Thursday, September 14, 2000

Part II

Environmental Protection Agency 40 CFR Part 148 et al. Hazardous Management System; Identification and Listing of : Inorganic Chemical Manufacturing ; Land Disposal Restrictions for Newly Identified Wastes; and CERCLA Hazardous Substance Designation and Reportable Quantities; Proposed Rule

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ENVIRONMENTAL PROTECTION made to RCRA Information Center, to: RCRA CBI Document Control Officer, AGENCY Crystal Gateway I, First Floor, 1235 Office of Solid Waste (5305W), U.S. Jefferson Davis Highway, Arlington, VA. EPA, 1200 Pennsylvania Avenue, NW, 40 CFR Parts 148, 261, 268, 271, and You also may submit comments Washington, D.C. 20460. Any CBI data 302 electronically by sending electronic should be specifically and clearly [SWH±FRL±6864±5] mail through the Internet to: marked. In addition, please submit a [email protected]. You non-CBI version of your comments for RIN 2050±AE49 should identify comments in electronic inclusion in the public record. format with the docket number F–2000– Supporting documents in the docket Hazardous ICMP–FFFFF. You must submit all System; Identification and Listing of for this proposal are also available in electronic comments as an ASCII (text) electronic format on the Internet: . Restrictions for Newly Identified Address requests for a hearing to Mr. Wastes; and CERCLA Hazardous We will keep the official record for David Bussard at: Office of Solid Waste, this action in paper form. Accordingly, Substance Designation and Reportable Hazardous Waste Identification Division Quantities we will transfer all comments received (5304W), U.S. Environmental Protection electronically into paper form and place AGENCY: Environmental Protection Agency, 1200 Pennsylvania Avenue, them in the official record, which also Agency. NW, Washington, D.C. 20460, (703) will include all comments submitted ACTION: Proposed rule. 308–8880. directly in writing. The official record is FOR FURTHER INFORMATION CONTACT: For the paper record maintained at the SUMMARY: The Environmental Protection general information, contact the RCRA/ RCRA Information Center, also referred Agency (EPA) proposes to amend the Superfund Hotline at (800) 424–9346 or to as the Docket. regulations for hazardous waste TDD (800) 553–7672 (hearing impaired). Our responses to comments, whether management under the Resource In the Washington, D.C., metropolitan the comments are written or electronic, Conservation and Recovery Act (RCRA) area, call (703) 920–9810 or TDD (703) will be in a notice in the Federal by listing as hazardous three wastes 412–3323. For specific aspects of the Register or in a response to comments generated from inorganic chemical rule, contact Ms. Gwen DiPietro, Office document placed in the official record manufacturing processes. We also of Solid Waste (5304W), U.S. for this rulemaking. We will not propose not to list as hazardous various Environmental Protection Agency, 1200 immediately reply to commenters other process wastes. This action Pennsylvania Avenue, NW, Washington, electronically other than to seek proposes to add the toxic constituents D.C., 20460. [E-mail addressee and clarification of electronic comments that found in the wastes to the list of telephone number: may be corrupted in transmission or constituents that serves as the basis for [email protected] (703–308– during conversion to paper form, as classifying wastes as hazardous, and to 8285).] For technical information on the discussed above. establish treatment standards for the CERCLA aspects of this rule, contact wastes. Ms. Lynn Beasley, Office of Emergency You may view public comments and The effect of this proposed regulation and Remedial Response, Analytical supporting materials in the RCRA would be to subject the wastes to Operations and Data Quality Center Information Center (RIC), located at stringent management and treatment (5204G), U.S. Environmental Protection Crystal Gateway I, First Floor, 1235 standards under Subtitle C of RCRA. Agency, 1200 Pennsylvania Avenue, Jefferson Davis Highway, Arlington, VA. Additionally, this action proposes to NW, Washington, D.C. 20460, [E-mail The RIC is open from 9 a.m. to 4 p.m., designate the wastes proposed for listing address and telephone number: Monday through Friday, excluding as hazardous substances subject to the [email protected] (703–603–9086).] federal holidays. To review docket Comprehensive Environmental materials, we recommend that you make SUPPLEMENTARY INFORMATION: If you do an appointment by calling 703–603– Response, Compensation, and Liability not submit comments electronically, we Act (CERCLA) and to adjust the one- 9230. You may copy a maximum of 100 ask you to voluntarily submit one pages from any regulatory docket at no pound statutory reportable quantities additional copy of your comments on (RQs) for some of these substances. charge. Additional copies cost $0.15/ labeled personal computer diskettes in page. DATES: EPA will accept public ASCII (text) format or a word processing comments on this proposed rule until format that can be converted to ASCII Customer Service November 13, 2000. Comments (text). It is essential to specify on the postmarked after this date will be How Can I Influence EPA’s Thinking on disk label the word processing software This Proposed Rule? marked ‘‘late’’ and may not be and version/edition as well as your considered. Any person may request a name. This will allow us to convert the In developing this proposal, we tried public hearing on this proposal by filing comments into one of the word to address the concerns of all our a request with Mr. David Bussard by processing formats we utilize. Please stakeholders. Your comments will help September 28, 2000. use mailing envelopes designed to us improve this rule. We invite you to ADDRESSES: If you wish to comment on physically protect the submitted provide your comments on all data, this proposed rule, you must send an diskettes. We emphasize that assumptions and methodologies used to original and two copies of the comments submission of comments on diskettes is support our proposal, your views on referencing docket number F–2000– not mandatory nor will it result in any options we have proposed, your ideas ICMP–FFFFF to: RCRA Information advantage or disadvantage to any on new approaches we have not Center, Office of Solid Waste (5305G), commenter. considered, any new data you may have, U.S. Environmental Protection Agency You should not submit electronically your views on how this rule may affect Headquarters, 1200 Pennsylvania any confidential business information you, and other relevant information. Avenue, NW, Washington, D.C. 20460. (CBI). You must submit an original and Your comments must be submitted by Hand deliveries of comments should be two copies of CBI under separate cover the deadline in this proposal. Your

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00002 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules 55685 comments will be most effective if you 4. Evaluation of Secondary Materials A. Applicability of Rule in Authorized follow the suggestions below: E. Description of Risk Assessment States • Explain your views as clearly as Approaches B. Effect on State Authorizations possible and provide a summary of the 1. What risk thresholds were used? VII. Designation of Inorganic Chemical reasoning you used to arrive at your 2. What leaching procedures were used? Wastes under the Comprehensive conclusions. Provide examples to 3. How were wastes screened to determine Environmental Response, Compensation, if further assessment was needed? and Liability Act (CERCLA) illustrate your views wherever possible. • 4. How was the groundwater pathway A. Reporting Requirements Provide solid technical data to evaluated? B. Basis for Proposed RQ Adjustment support your views. • 5. How was the surface water pathway VIII. Administrative Assessments If you estimate potential costs, evaluated? A. Executive Order 12866 explain how you arrived at your 6. What are the limitations and 1. Methodology Section estimate. uncertainties of the assessment? 2. Results • Tell us which parts of this proposal F. Sector-specific Listing Determination B. Regulatory Flexibility Act (RFA), as you support, as well as which parts you Rationales amended by the Small Business disagree with. 1. Antimony oxide Regulatory Enforcement Fairness Act of • Offer specific alternatives. 2. Barium carbonate 1996 (SBREFA), 5 U.S.C. 601 et seq. • Reference your comments to 3. Boric acid C. Paperwork Reduction Act specific sections of the proposal by 4. Cadmium pigments D. Unfunded Mandates Reform Act using section titles or page numbers of 5. Inorganic hydrogen cyanide E. Executive Order 12898: Environmental the preamble or the regulatory citations. 6. Phenyl mercuric acetate Justice • Clearly label any CBI submitted as 7. Phosphoric acid from the dry process F. Executive Order 13045 : Protection of 8. Phosphorus pentasulfide Children From Environmental Health part of your comments. 9. Phosphorus trichloride • Include your name, date, and Risks and Safety Risks 10. Potassium dichromate G. Executive Order 13084: Consultation docket number with your comments. 11. Sodium chlorate and Coordination With Indian Tribal Contents of This Proposed Rule 12. Sodium dichromate Governments 13. Sodium phosphate from wet process H. Executive Order 13132: Federalism I. Overview phosphoric acid I. National Technology Transfer and A. Who Potentially Will be Affected by this 14. Titanium dioxide Advancement Act Proposed Rule? G. What is the Status of Leachate B. Why Does this Rule Read Differently from Previously Disposed Wastes? I. Overview from Other Listing Rules? IV. Proposed Treatment Standards Under A. Who Potentially Will Be Affected by C. What are the Statutory Authorities for RCRA’s Land Disposal Restrictions this Proposed Rule? A. What are EPA’s Land Disposal This Proposed Rule? II. Background Restrictions (LDRs)? A. How Does EPA Define a Hazardous Beginning January 1, 1999 all B. What are the treatment standards for Waste? K176 (baghouse filters from production documents related to EPA’s regulatory, B. How Does EPA Regulate RCRA of antimony oxide) compliance and enforcement activities, Hazardous Wastes? C. What standards are the treatment including rules, policies, interpretive C. What is the Consent Decree Schedule for guidance, and site-specific and Scope of this Proposal? standards for K177 (slag from the III. Approach Used in this Proposed Listing production of antimony oxide that is determinations with broad application, A. Summary of Today’s Action disposed of or speculatively should properly identify the regulated B. What Wastes Associated with the 14 accumulated)? entities, including descriptions that Sectors Are Outside the Scope of the D. What are the treatment standards for correspond to the applicable SIC codes Consent Decree? K178 (nonwastewaters from the or NAICS codes (source: October 9, 1998 1. Mineral processing wastes exempt under production of titanium dioxide by the USEPA memo from Peter D. Robertson, the ‘‘Bevill’’ exemptions chloride-ilmenite process)? E. What Other LDR Provisions Are Acting Deputy Administrator of 2. Residuals used or reused in different USEPA). Today’s action, if finalized, industrial processes Proposed to Apply? 3. Debris and other nonprocess wastes 1. Debris could potentially affect those who C. What Information Did EPA Collect and 2. Soil handle the wastes that we are proposing Use? 3. Underground Injection Wells that can be to add to EPA’s list of hazardous wastes 1. The RCRA Section 3007 Survey found in the administrative record for under the RCRA program. This action 2. Field work: site visits, sampling and this rule also may affect entities that may need to analysis F. Is There Treatment Capacity for the respond to releases of these wastes as 3. Other sources Proposed Wastes? CERCLA hazardous substances. These 1. What Is a Capacity Determination? D. How Did EPA Evaluate Wastes for potentially-affected entities are Listing Determinations? 2. What are the Capacity Analysis Results? 1. Listing policy V. Compliance Dates described in the Economics Background 2. Characteristic hazardous waste A. Notification Document placed in the docket in 3. Evaluations of particular units and B. Interim Status and Permitted Facilities support of today’s proposed rule. A pathways of release VI. State Authority summary is shown in the table below.

SUMMARY OF FACILITIES POTENTIALLY AFFECTED BY THE USEPA'S 2000 INORGANIC CHEMICAL MANUFACTURING WASTE LISTING PROPOSAL

Number of U.S. relevant Item SIC code Industry sector name inorganic mfg. facilities

1 ...... 2816 Inorganic Pigments ...... 3 1 ...... 2819 Industrial Inorganic Chemicals, not elsewhere classified ...... 3

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The list of potentially affected entities II. Background wastes are also classified as hazardous in the above table may not be wastes based on the ‘‘derived-from’’ rule A. How Does EPA Define a Hazardous exhaustive. Our aim is to provide a (see 40 CFR 261.3(c)(2)(i)). For example, Waste? guide for readers regarding entities ash or other residuals from the likely to be regulated by this action. Section 3001 of RCRA and EPA’s treatment of a listed waste generally This table lists those entities that we are regulations establish two ways of carries the original hazardous waste aware potentially could be affected by identifying wastes as hazardous under code and is subject to the hazardous this action. However, this action may RCRA. A waste may be hazardous either waste regulations. Also, the ‘‘mixture’’ affect other entities not listed in the if it exhibits certain properties (called rule (see 40 CFR 261.3(a)(2)(iii) and (iv)) table. To determine whether your ‘‘characteristics’’) which pose threats to provides that, with certain limited facility is regulated by this action, you human health and the environment, or exceptions, any mixture of a listed should examine 40 CFR Parts 260 and if it is included on a specific list of hazardous waste and a solid waste is 261 carefully in concert with the wastes EPA has evaluated and found to itself a RCRA hazardous waste. proposed rules amending RCRA that are pose unacceptable risks. EPA’s Some materials that would otherwise found at the end of this Federal Register regulations in the Code of Federal be classified as hazardous wastes under document. If you have questions Regulations (CFR) define four hazardous the rules described above are excluded regarding the applicability of this action characteristics: ignitability, corrosivity, from jurisdiction under RCRA if they to a particular entity, consult the person reactivity, or toxicity. (See 40 CFR are recycled in certain ways. The listed in the preceding section entitled 261.21 through 261.24.) As a generator, current definition of solid waste at 40 CFR 261.2 excludes secondary materials FOR FURTHER INFORMATION CONTACT. you must determine whether or not a waste exhibits any of these from the definition of solid waste that B. Why Does This Rule Read Differently characteristics by testing the material or are used directly (i.e., without From Other Listing Rules? by using your knowledge of the process reclamation) as ingredients in that produced the waste. (See 40 CFR manufacturing processes to make new Today’s proposed listing 262.11(c).) products, used directly as effective determination preamble and regulations EPA may also conduct a more specific substitutes for commercial products, or are written in ‘‘readable regulations’’ assessment of a waste or category of returned directly to the original process format. The authors tried to use active wastes and ‘‘list’’ them if they meet from which they are generated as a rather than passive voice, plain criteria set out in 40 CFR 261.11. As substitute for raw material feedstock. language, a question-and-answer format, described in 40 CFR 261.11, we may list (See 40 CFR 261.2(e).) As discussed in the pronouns ‘‘we’’ for EPA and ‘‘you’’ a waste as hazardous if it: the January 4, 1985, rulemaking that for the owner/generator, and other —Exhibits any of the characteristics promulgated this regulatory framework, techniques to make the information in noted above , i.e., ignitability, these are activities which, as a general today’s rule easier to read and corrosivity, reactivity, or toxicity matter, resemble ongoing manufacturing understand. This new format is part of operations more than conventional (261.11(a)(1)); waste management and so are more our efforts toward regulatory re- —Is ‘‘acutely’’ hazardous, i.e., if they are appropriately classified as not involving invention, and it makes today’s rule fatal to humans or in animal studies solid wastes. (See 50 FR 637–640). Our read differently from other listing rules. at low doses, or otherwise capable of approach to these issues is described in We believe that this new format will causing or significantly contributing more detail below in section III.D.4. help readers understand the regulations, to an increase in serious illness which should then increase compliance, (261.11(a)(2)); or B. How Does EPA Regulate RCRA make enforcement easier, and foster —Is capable of posing a substantial Hazardous Wastes? better relationships between EPA and present or potential hazard to human the regulated community. Wastes exhibiting any hazardous health or the environment when characteristic or listed as hazardous are C. What Are the Statutory Authorities improperly managed (261.11(a)(3)). subject to federal requirements under for This Proposed Rule? Under the third criterion at 40 CFR RCRA. These regulations affect persons 261.11(a)(3), we may decide to list a who generate, transport, treat, store or These regulations are proposed under waste as hazardous (1) if it contains dispose of such waste. Facilities that the authority of Sections 2002(a), hazardous constituents identified in must meet the hazardous waste 3001(b), 3001(e)(2), 3004(d)–(m) and Appendix VIII to 40 CFR Part 261, and management requirements, including 3007(a) of the Solid Waste Disposal Act, (2) if, after considering the factors noted the need to obtain permits to operate, 42 U.S.C. 6912(a), 6921(b) and (e)(2), in this section of the regulations, we commonly are referred to as ‘‘Subtitle 6924(d)–(m)and 6927(a), as amended ‘‘conclude that the waste is capable of C’’ facilities. Subtitle C is Congress’ several times, most importantly by the posing a substantial present or potential original statutory designation for that Hazardous and Solid Waste hazard to human health or the part of RCRA that directs EPA to issue Amendments of 1984 (HSWA). These environment when improperly treated, those regulations for hazardous wastes statutes commonly are referred to as the stored, transported, or disposed of, or as may be necessary to protect human Resource Conservation and Recovery otherwise managed.’’ We place a health or the environment. EPA Act (RCRA), and are codified at Volume chemical on the list of hazardous standards and procedural regulations 42 of the United States Code (U.S.C.), constituents on Appendix VIII only if implementing Subtitle C are found Sections 6901 to 6992(k) (42 U.S.C. scientific studies have shown a generally at 40 CFR Parts 260 through 6901–6992(k)). chemical has toxic effects on humans or 272. Section 102(a) of the Comprehensive other life forms. When listing a waste, All RCRA hazardous wastes are also Environmental Response, we also add the hazardous constituents hazardous substances under the Compensation, and Liability Act of 1980 that serve as the basis for listing to Comprehensive Environmental (CERCLA), 42 U.S.C. 9602(a) is the Appendix VII to part 261. Response, Compensation, and Liability authority under which the CERCLA Residuals from the treatment, storage, Act (CERCLA), as described in section aspects of this rule are proposed. or disposal of most listed hazardous 101(14)(C) of the CERCLA statute. This

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00004 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules 55687 applies to wastes listed in 40 CFR Today’s proposal satisfies EPA’s duty tetrachloride production exempt 261.31 through 261.33, as well as any under paragraph 1.g to propose under 40 CFR 261.4(b)(7).) (T) wastes that exhibit a RCRA determinations for inorganic chemical We found that all of the remaining characteristic. Table 302.4 at 40 CFR industry wastes. wastes that we evaluated did not meet 302.4 lists CERCLA hazardous As described above, the consent the criteria for listing in 40 CFR 261.11, substances along with their reportable decree provides that EPA does not need and we are proposing not to list them as quantities (RQs). Anyone spilling or to make listing determinations for hazardous wastes. More information on releasing a substance at or above the RQ certain wastes that it has exempted from our evaluations of particular wastes is must report this to the National hazardous waste regulations under the set out in the background documents Response Center, as required in ‘‘Bevill amendments’’ to RCRA. See the and the sector-specific discussions in CERCLA Section 103. In addition, discussion of ‘‘exempt mineral section III.F of this preamble. Section 304 of the Emergency Planning processing’’ wastes in section III.B.1 We have previously listed as and Community Right-to-Know Act below. hazardous a number of wastes in 40 CFR (EPCRA) requires facilities to report the 261.32 from other inorganic chemicals III. Approach Used in This Proposed release of a CERCLA hazardous industries, including wastes from the Listing substance at or above its RQ to State and production of inorganic pigments (codes local authorities. Today’s rule proposes A. Summary of Today’s Action K002 through K008), and wastes from to establish RQs for some of the newly Manufacturers of the inorganic chlorine production (codes K071, K073, and K106). Today’s proposal does not listed wastes. chemical products described above affect the scope of any existing identified over 170 categories of C. What Is the Consent Decree Schedule hazardous waste listing, and we are not residuals generated as part of their for and Scope of This Proposal? soliciting comments on those existing production processes. We first The 1984 Hazardous and Solid Waste listing determinations. determined which of these residuals fell Amendments (HSWA) to RCRA require We are also proposing other changes within the scope of our consent decree EPA to make listing determinations for to the RCRA regulations as a result of obligations. We then evaluated the risks several specified categories of wastes, the proposed listings. These changes posed by each of the remaining including ‘‘inorganic chemical industry include adding constituents to categories of residual materials. In some wastes’’ (see RCRA section 3001(e)(2)). Appendices VII and VIII for Part 261, cases we used quantitative or qualitative In 1989, the Environmental Defense and setting new land disposal screening methods. For 18 wastes we Fund (EDF) filed a lawsuit to enforce restrictions. We are proposing to add the conducted full-scale modeling to predict the statutory deadlines for listing following constituents to Appendix VII risks. decisions in RCRA Section 3001(e)(2). that serve as the basis for listing: K176— As a result of this evaluation, we (EDF v. Browner; D.D.C. Civ. No. 89– arsenic and lead, K177—antimony, and found that three wastes generated in the 0598). To resolve most of the issues in K178—manganese and thallium. We are 14 inorganic chemicals manufacturing the case, EDF and EPA entered into a also proposing to add manganese to the operations which we evaluated meet the consent decree, which has been list of hazardous constituents in criteria for listing set out in either 40 amended several times to revise Appendix VIII, based on scientific CFR 261.11(a)(1) or 261.11(a)(3). We deadlines for EPA action. Paragraph 1.g studies that demonstrate manganese has conducted full-scale modeling of two of (as amended) of the consent decree toxic effects on humans and other life these wastes and propose to list them addresses the inorganic chemical forms. Section IV of today’s proposal under 40 CFR 261.11(a)(3). We found industry: describes the proposed changes to the that one waste warranted listing under land disposal restrictions, which would EPA shall promulgate a final listing 40 CFR 261.11(a)(1) because it exhibited establish treatment standards for determination for inorganic chemical hazardous waste characteristics. We did specific constituents in the wastes industry wastes on or before October 31, not model this waste. Since these are 2001. This listing determination shall be proposed for listing. proposed for public comment on or before wastes from specific inorganic chemical Also as a result of the proposed August 30, 2000. The listing determination industries, we propose to add them to listings, these wastes would become shall include the following wastes: sodium Section 261.32 with K-waste codes. The hazardous substances under CERCLA. dichromate production wastes, wastes from three wastestreams we propose to list as Therefore, in today’s rule we are the dry process for manufacturing hazardous, along with their proposing to designate these phosphoric acid, phosphorus trichloride corresponding hazard code and wastestreams as CERCLA hazardous production wastes, phosphorus pentasulfide proposed EPA Hazardous Waste substances, and to adjust the one-pound production wastes, wastes from the Numbers, are: 1 statutory RQs for two of these production of sodium phosphate from wet K176 Baghouse filters from the process phosphoric acid, sodium chlorate wastestreams; this is described in production wastes, antimony oxide production of antimony oxide. (E) section VII of today’s proposal. production wastes, cadmium pigments K177 Slag from the production of antimony oxide that is disposed of or B. What Wastes Associated With the 14 production wastes, barium carbonate Sectors Are Outside the Scope of the production wastes, potassium dichromate speculatively accumulated. (T) production wastes, phenyl mercuric acetate K178 Nonwastewaters from the Consent Decree? production wastes, boric acid production production of titanium dioxide by the Determining the scope of our consent wastes, inorganic hydrogen cyanide chloride-ilmenite process. (This decree obligations was more production wastes, and titanium dioxide listing does not apply to chloride complicated than usual for two reasons. production wastes (except for chloride process waste solids from titanium First, Paragraph 1.g (quoted above in process waste solids). However, such listing II.C) does not tell EPA which determinations need not include any wastes 1 which are excluded from hazardous waste As required in 40 CFR 262.30, the listing wastestreams it must evaluate. For most description includes the hazard code. Wastes listed other listing obligations set out in the regulation under section 3001(b)(3)(A)(ii) of under 40 CFR 261.11(a)(1) due to the toxicity RCRA and for which EPA has determined characteristic are designated ‘‘E,’’ and wastes listed consent decree, the decree specifies that such regulation is unwarranted pursuant under 40 CFR 261.11(a)(3) for toxicity are particular wastestreams which EPA to section 3001(b)(3)(C) of RCRA. designated ‘‘T’’. must evaluate for listing. See, for

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00005 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55688 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules example, paragraph 1.k identifying 14 (Sept. 1, 1989), 55 FR 2322 (Jan. 23, wastes: Boric acid, sodium dichromate, specific petroleum wastestreams.2 1990), the July 31, 1990 Report to and titanium dioxide. Second, paragraph 1.g contains an Congress on Wastes from Mineral In other sectors, the facilities produce exemption for wastes found to be Processing, and 56 FR 27300 (June 13, inorganic product chemicals from a exempt from hazardous waste regulation 1991). mineral product. Under the Bevill in previous EPA actions implementing EPA codified these ‘‘Bevill’’ exemption (54 FR 36620–21), chemical the so-called ‘‘Bevill exemptions’’ for exemptions at 40 CFR 261.4 (b)(7). EPA manufacturing begins if there is any mineral processing wastes. Thus, we discussed some of these exemptions further processing of a saleable mineral needed to conduct some analysis to further in a 1998 final rule promulgating product. Since these facilities use determine the scope of our obligations. treatment standards for non-exempt saleable mineral products as feedstock, We began by asking facilities to mineral processing wastes that exhibit their processes are chemical identify all of the residuals generated by the toxicity characteristic. See the Land manufacturing, and may not be their production processes. We then Disposal Restrictions Phase IV Final classified as mineral processing. reviewed their lists. We found that some Rule at 63 FR 28598 (May 26, 1998). Therefore, none of the wastestreams residuals were actually exempt ‘‘Bevill’’ Paragraph 1.g of the consent decree generated by these facilities in the wastes that we need not address. We provides that EPA need not make listing production of the other inorganic found that other wastes were really determinations for wastes from any of chemicals are Bevill exempt. associated with the manufacture of the 14 inorganic chemical We emphasize that we are not re- other materials. Also, we concluded that manufacturing processes which are opening any Bevill decisions made in a few residuals were not ‘‘production’’ ‘‘excluded from hazardous waste earlier actions regarding the wastes and therefore were not covered regulation under Section exemptions. We are not re-defining the boundaries between ‘‘extraction’’ and by the decree. With the exceptions 3001(b)(3)(A)(ii) of RCRA and for which ‘‘beneficiation,’’ between discussed below in our evaluation of the it has determined that such regulation is ‘‘beneficiation’’ and ‘‘mineral sodium dichromate and titanium unwarranted pursuant to Section processing,’’ or between ‘‘mineral dioxide sectors, we chose not to 3001(b)(3)(C) of RCRA.’’ In other words, processing’’ and non-exempt chemical evaluate any of the wastes that we the consent decree does not require us manufacturing. Nor are we revisiting considered to be outside the scope of to make listing determinations for our decision that all wastes uniquely the decree. We concluded that wastes which we exempted under the associated with the extraction and evaluation was not possible under the statute’s ‘‘Bevill’’ provisions. time frame set out in the decree. In the beneficiation of ores and minerals are Paragraph 1.g. of the consent decree following sections we provide an exempt. Similarly, we are not re- requires EPA to make a listing overview of the types of wastes that we opening any of our earlier decisions as determination for ‘‘* * * titanium consider outside the scope. to which categories of mineral dioxide production wastes (except for processing wastes are exempt. Rather, 1. Mineral Processing Wastes Exempt chloride process waste solids).’’ EPA we are determining whether particular Under the ‘‘Bevill’’ Exemptions interprets the exception to refer to the wastestreams fall within any of the Many of the inorganic chemical chloride process waste solids from the exempt categories. We are not manufacturing processes we address in production of titanium tetrachloride requesting comment on, and do not this rule use ores and minerals as which are exempt under the Bevill rule, intend to respond to comments relating feedstocks. Some wastes derived from rather than all solids from the chloride to the earlier decisions. the processing of ores and minerals are process. Solids generated after titanium We also found that some inorganic exempt from regulation as RCRA tetrachloride forms fall within the scope chemical processes generate composite hazardous wastes under decisions EPA of the consent decree. wastestreams that contain both a Bevill made under statutory requirements We reviewed the generators’ lists of exempt waste and one or more non- known as the ‘‘Bevill’’ amendments. process residuals to determine whether exempt wastes. We evaluated the non- RCRA Sections 3001(b)(3) and 8002(p) they had included any Bevill exempt exempt portions of such wastes to fulfill required EPA to determine whether wastes which we need not assess. (In our consent decree requirements. We wastes from the extraction, beneficiation some cases, the generators had claimed apportioned risks between the exempt or processing of ores and minerals that certain wastes were exempt under and nonexempt portion of such warranted regulation as hazardous EPA’s Bevill decisions.) This process commingled wastes, and made listing wastes under Subtitle C of RCRA. was not always simple. We found it was determinations for the non-exempt Between 1989 and 1991 EPA completed sometimes difficult to determine portions. We did not, however, assess a series of rules and studies establishing whether a particular facility’s waste fit the exempt portions of such streams. which mining wastes fit within the within one of the exempt categories. For This assessment, therefore, does not re- ‘‘extraction,’’ ‘‘beneficiation,’’ or example, the mineral processing open any earlier decision regarding ‘‘processing’’ definitions, and which of exemption for titanium dioxide covers exemptions for the ‘‘Bevill’’ component the wastes within each category were only solid materials from an initial step of the commingled streams. exempt from regulation as hazardous in the production process. It was not always easy to tell whether particular 2. Residuals Used or Reused in Different wastes. EPA concluded that all wastes Industrial Processes produced during extraction and waste solids were generated from the beneficiation are entitled to an portion of the process that would make In some cases, facilities within the 14 exemption. EPA found that 20 them exempt, or from later production inorganic chemicals sectors set out in categories of wastes from subsequent steps. Sector-specific information the consent decree produce residuals ‘‘mineral processing’’ operations met the regarding our conclusions appears in that are used or reused in processes that ‘‘high volume/low toxicity’’ criteria and section III.F of this preamble for those are not among those listed in the decree. were exempt as well. See 54 FR 36592 sectors where we found this exemption Those industries in turn produced had some relevance. We found that residuals derived from the materials 2 The revised consent decree is available in the facilities in only three of the consent generated in the consent decree docket for today’s proposal. decree sectors generate Bevill exempt industries. We evaluated the

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00006 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules 55689 management of the original industry’s bricks which become wastes when included the development, distribution, material up to the point that the second facilities remove them to refurbish their and assessment of an extensive industry inserts it into its production furnaces. We consider this material to questionnaire sent under the authority process. However, we generally be a structural component of the plant of RCRA section 3007 to all known considered the second production where production takes place rather facilities engaged in any of the 14 process and its associated wastes to be than a waste from the ‘‘production’’ of inorganic chemical manufacturing beyond the scope of the consent decree. an inorganic chemical. Similarly, we processes. During our field We did not evaluate for listing purposes consider a few analogous types of plant investigations we made site visits to wastes generated from these non- debris to fall outside the scope of the familiarize ourselves with processes and consent decree industries. For example, decree. This debris includes residuals, and made additional visits to in the titanium dioxide sector, one miscellaneous construction materials, collect samples of residuals which we facility uses a residual from the insulation, reactor bed material, and sent to laboratories for analysis. Finally, production of titanium dioxide as an piping. These wastes were reported for we collected data from other sources to ingredient to make salt. We considered the following inorganic sectors: help characterize the settings in which salt-making to be a separate production Phosphoric acid, barium carbonate, some of the wastes are managed. Each process outside the scope of the consent sodium dichromate, hydrogen cyanide, of these efforts is summarized below. decree. We are not proposing any listing antimony oxide, sodium phosphate, and 1. The RCRA Section 3007 Survey determinations for wastes generated in titanium dioxide. the salt plant. We have never interpreted the decree We developed an extensive However, in some cases, the reuse of to require us to consider listing tanks, questionnaire under the authority of the residual from a consent decree pads, or other structural components Section 3007 of RCRA for distribution to process involved an activity which we housing production processes when the inorganic chemicals manufacturing always regulate as waste management. they become wastes by being removed industry. The purpose of the survey was In this situation, we considered the from use. Other paragraphs of the decree to gather information about solid and reuse to be waste management, and the support this position. Paragraphs 1.c. hazardous waste generation and waste to be within the scope of the (coke byproducts) and 1.k. (petroleum management practices in the U.S. for the consent decree. Consequently, we refining wastes) cover production fourteen inorganic chemical industry evaluated the residual for listing. For processes involving reaction vessels sectors. The questionnaire collected example, we found that one of the lined with refractory or similar information about the inorganic facilities which produces boric acid materials, and in neither case did the chemical products manufactured, the generates a waste which is used as a decree include wastes related to the processes used, the wastes generated, fuel. Under our regulations, reaction vessels themselves or related the wastes characteristics, and how the we regulate burning for energy recovery materials. Nor do any other provisions wastes were managed. The and so, we evaluated this waste. See 40 in the decree direct us to list any other questionnaire is included in the CFR 261.2(c)(2). We found that the type of structural components. We note ‘‘General Background Document for the waste is already being managed in a that discarded refractory bricks and Inorganic Chemical Listing RCRA Subtitle C unit and decided not other debris would be regulated as Determination.’’ which is in the docket to list the waste. Others examples of hazardous wastes, if these materials for today’s proposal. This document reuse that we evaluated include land were contaminated with a listed waste also provides more details on the application of biological treatment (including wastes listed as a result of producers identified in the inorganic solids from hydrogen cyanide today’s rulemaking), or if they exhibited sectors. production as a fertilizer or soil a hazardous waste characteristic. We distributed the survey in March of amendment, and land application of A few facilities also reported 1999 to all 124 facilities that we had gypsum from the titanium dioxide environmental media (excavated soils or identified as potential manufacturers of sector. In two cases, however, we recovered groundwater) contaminated chemicals in the 14 targeted sectors. We decided to make listing decisions for with process residuals as wastes from developed the list of facilities from a residuals generated during the their production processes. We consider review of the available literature, which production of non-consent decree such contaminated media to be outside included directories of chemical products. In the titanium dioxide sector, the scope of today’s listing producers, reference works of chemical the residuals are commingled with other determinations, because these are not technology, chemical profile wastes clearly within the scope of the wastes generated during production information, and previous work by EPA decree. See the discussions of the processes, but rather wastes generated on these industries. From the surveys sodium dichromate sector and the due to construction or remedial action. distributed, 57 facilities indicated that titanium dioxide sector in section III.F. We note that none of the other consent they manufacture chemicals from at In the sodium dichromate sector, decree provisions require us to evaluate least one of the 14 sectors. The other residuals from the non-consent decree contaminated media. See the specific facilities notified us that they had either process are piped back to the consent listing background documents for the stopped operations or did not decree process, making it difficult to different sectors for a full listing of the manufacture inorganic chemical determine whether the two processes wastes we considered to be out of scope products. From the survey, we are really separate. of the decree. confirmed that one product was no longer manufactured in this country 3. Debris and Other Nonprocess Wastes C. What Information Did EPA Collect (phenyl mercuric acetate). Some generators also identified debris and Use? We also conducted an exhaustive and structural components of their Our investigation of the wastes engineering review of the submitted production plants as intermittently- generated by the inorganic chemicals surveys for accuracy and completeness. generated wastes. We concluded that manufacturing industry included two We conducted quality assurance these materials do not fall within the major information collection efforts: A reviews of the data to identify any scope of the decree. Most of the wastes survey of the industries and field inappropriate entries and missing data. that fell in this category were refractory investigations. The survey effort The engineering review of each facility’s

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00007 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55690 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules response resulted in follow-up letters During record sampling, we collected inorganic hydrogen cyanide industry for and/or telephone calls to the facilities 69 waste samples from 13 different cyanide and volatile organics because of seeking clarifications, corrections, and facilities. Additional samples were their potential to be present from the additional data where needed. collected for QA/QC purposes. Largely process. Similarly, in the titanium Where we conducted sampling and due to the time constraints imposed by dioxide sector, we analyzed waste analysis of the waste, we used this our consent decree schedule, we samples for semivolatile and analytical data in our analysis (see the focused the sampling effort on the chlorinated organics due to the use of following section). Facilities also wastes that we most expected to present coke and chlorine as raw materials in submitted data in their survey on the significant potential risks. Based on the production process for the titanium composition of some of their wastes. In information obtained from the RCRA chloride intermediate. The overall list of the absence of our own analytical data, Section 3007 Surveys, we established target analytes are in the QAPP, which we used data provided by facilities in sampling priorities by considering the is in the docket for today’s rule. The our evaluation. These cases are noted in reported management practices (e.g., docket also contains the background the sector-specific discussions in wastes going to Subtitle D and documents for each sector and the section III.F. In some cases, these data impoundments were of concern), and corresponding waste characterization consisted of results from testing to the likely presence of contaminants of data reports, which show the chemical determine whether the wastes exhibited concern. analyses performed and the analytes characteristics. We thought such data We also found that we were able to found in the waste samples. were reliable because of the make listing decisions on a variety of In our analyses of wastes samples, we consequences the facilities would face if reported wastes without conducting performed analyses to measure their characteristic data were not sampling. In some cases, we were able constituent concentrations in the wastes accurate. In addition, survey to use information about the processes themselves (‘‘total’’ analysis), as well as respondents were required to certify the and the raw materials to conclude that analyses for constituents that leach out accuracy of their submittal. a waste was not likely to present a of the wastes. We generally used the significant risk. Also, we did not methods specified in OSW’s methods 2. Field Work: Site Visits, Sampling and typically sample wastes that were manual (‘‘Test Methods for Evaluating Analysis reported to be characteristically Solid Waste, Physical/Chemical As part of our field work, we visited hazardous waste and were already Methods,’’ SW–846), as described in the regulated as hazardous under RCRA. We QAPP, the SAPs, and the background production facilities (engineering site felt that, for these wastes, we could documents for the specific sectors. We visits), we took preliminary samples make listing decisions without further used two extraction methods to measure (familiarization sampling), and we information on waste constituents. In leaching, the Toxicity Characteristic obtained samples to fully characterize addition, we did not attempt to sample Leaching Procedure (TCLP, SW–846 the waste for constituents of concern wastes that we found to be outside the method 1311), and the Synthetic (record sampling). We initiated the scope of the consent decree, as Precipitation Leaching Procedure (SPLP, sampling phase of this listing described in Section III.B. Thus, for SW–846 method 1312). determination with the development of example, we did not sample a number In general, we were able to measure a Quality Assurance Project Plan of wastes that appeared to be exempt the concentrations of constituents in (QAPP) for sampling and analysis. The under the Bevill regulations. waste samples at very low detection QAPP describes the quality assurance We believe that the 69 record samples levels. However, for some constituents and quality control requirements for the from 13 sites provide an adequate in some matrices the SPLP and/or TCLP data collection. We also developed characterization of the wastes that we analyses provided detection limits that sampling and analysis plans (SAPs) for sampled. The 13 sites represent were somewhat above health-based sampling at individual facilities. The approximately 30% of the 42 identified levels of concern. In such cases, we QAPP and the SAPs are available in the production facilities within the specific examined all of the analytical data to public docket for this proposal. sectors we chose for sampling. The determine if the undetected constituent The primary purpose of the wastes sampled also represent the major might possibly present a potential risk. engineering site visits was to gain first waste types of concern, e.g., specific Where we did not detect the constituent hand knowledge of the manufacturing process wastes/sludges, wastewater in the total analysis (i.e., the analysis of processes, the waste generation and treatment sludges, wastewaters, and a sample prior to any leaching), we management, and to identify potential spent filter material. Section III.F of this assumed that the constituent was not locations for waste sampling. We proposal provides information on the present in the leachate. However, if the conducted site visits at 25 facilities in specific wastes sampled in each sector. totals analysis showed the presence of a 12 of the sectors. We selected the The docket for today’s proposal also constituent that we did not detect in the facilities to visit based on logistics and contains background documents for the leachate, then we assessed the risk that to visit sites that represent the variety of specific sectors, which give details on would be posed if the constituent were process and wastes generated within which wastes we sampled and our present at a concentration equal to one- industry sectors. Site visit reports are evaluation of the need for sampling or half the detection limit. Section III.F available in the docket for today’s rule. modeling certain wastes. shows the cases where we used this During some of the engineering site For most sectors, we focused our assumption in our evaluation of wastes visits, we collected 22 familiarization analyses on metal constituents, because for the different inorganic sectors, and samples to help us identify potential these are the constituents expected from further details are available in the sampling or analytical problems for the the inorganic processes under background documents for each sector. wastes of interest. For example, we used evaluation. We analyzed for other the familiarization samples to assess the constituents in those cases where we 3. Other Sources effectiveness of the analytical methods expected they might be present in the We also collected data from a variety that we planned to use during record waste, or if other constituents showed of other sources to help characterize the sampling for a number of the targeted up in the familiarization sampling. settings in which these wastes are waste matrices. Thus, we analyzed wastes from the managed. For example, we contacted

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00008 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules 55691 several state and local authorities to regulatory actions (261.11(a)(3)(vii) and full-scale risk modeling for 18 wastes in collect information regarding the 261.11(a)(3)(x)) in selecting the waste 5 sectors. We found that we could location of drinking water wells. We management scenarios we evaluated in adequately address the risks of the also obtained information and, in some our risk assessments. For example, we remaining wastes with a variety of less cases analytical data, from state used information that the waste time-consuming approaches. Some were authorities and other sources to help in generators submitted in their Section qualitative; others were quantitative, but our evaluations. We note these sources 3007 questionnaires to decide what not as complex as full modeling. in the sector-specific discussions in types of waste management units are We evaluated one waste using the Section III.F when we relied on such used. Using information about other single criterion set out in 40 CFR data. federal environmental regulatory 261.11(a)(1) rather than the eleven programs, we concluded that some units factors referenced in 40 CFR D. How Did EPA Evaluate Wastes for or some pathways did not pose risks 261.11(a)(3). This is the first time under Listing Determinations? requiring evaluation. this consent decree that we have 1. Listing Policy We separately considered the proposed to make a listing decision As discussed in section II.A. of this remaining factor, whether the available based on this criterion. It relies on the preamble, we consider the listing information indicated any impact on existing characteristics to identify criteria set out in 40 CFR 261.11, in light human health or the environment from wastes posing significant risks and does of all the information we have relevant improper management of the wastes of not require the use of modeling. See the concern (261.11(a)(3)(ix)). Thus, we discussion of wastes from the to the criteria, in making listing examined a variety of databases for production of antimony oxide in section determinations. For decisions made information on damage incidents for the III.F.1 of the preamble. under 40 CFR 261.11(a)(3), today’s inorganic chemical production Our proposed listing determinations proposed listing determinations follow processes under investigation. For are based upon estimates of individual the elements of the EPA’s hazardous example, we examined databases for risk. We relied on individual risk waste listing policy presented the information on potential and actual estimates (HQs > 1), and not population proposed listing for wastes generated by Superfund sites (CERCLIS), releases risk estimates, because we are the dyes and pigments industry (see FR reported under the Toxic Release concerned about risks to individuals 66072, December 22, 1994). We have Inventory System (TRIS), civil cases who are exposed to potential releases of modified and adapted this policy in filed on behalf of EPA, and spills and hazardous constituents. We believe that subsequent listings. See for example the releases reported to the National using individual risk as a basis for our recent Petroleum Refining proposal (60 Response Center (NRC). A full listing determinations (rather than FR 57747; November 20, 1995) and the description of our search is in the population risk estimates) also is Solvents waste proposal (61 FR 42318; docket for this rule. appropriate to protect against potential August 14, 1996). Most of the cases found for these risks, as well as present risks that may This policy uses a ‘‘weight-of- industries typically resulted from spills arise due to the generation and evidence’’ approach in which calculated or releases of products, and did not management of particular wastestreams. risk information is a key factor to provide any useful information of EPA acknowledges that in cases where consider in making a listing possible risks presented by the wastes small populations are exposed to determination under 40 CFR we evaluated for listing. In a few cases particular wastes and waste 261.11(a)(3). The criteria provided in 40 we found sites on the Superfund management practices, population risks CFR 261.11(a)(3) include eleven factors National Priority List (NPL) that may be very small. We did not attempt for determining ‘‘substantial present or included inorganic manufacturing to calculate population risks for the potential hazard to human health and processes. However these sites usually proposed listings. In general, we expect the environment.’’ We incorporate nine encompassed a variety of chemical population risks arising from of these factors, as described generally manufacturing and mining industries, contaminated groundwater due to waste below, into our risk evaluation for the and it is difficult to attribute the damage management to be small, because often wastestreams of concern: reported to the specific inorganic only a limited number of domestic wells —Toxicity (261.11(a)(3)(i)) is considered manufacturing wastes under evaluation. will be near these facilities, and in developing the health benchmarks Furthermore, contamination at these groundwater contamination often moves used in the risk evaluation. sites appears linked to historical very slowly. Nevertheless, the increased —Constituent concentrations and waste management practices at closed or risk for an exposed individual may be quantities (261.11(a)(3)(ii) and inactive manufacturing plants, and significant. In proposing the listing 261.11(a)(3)(viii)) are used to define these were not useful in assessing determinations for K176, K177, and the initial conditions for the risk current or potential hazards for the K178, EPA is protecting against the evaluation. wastes at issue. In addition, Federal and potential risk for exposed individuals, —Potential to migrate, persistence, State regulatory controls are now in regardless of how many individuals are degradation, and bioaccumulation of place that would prevent exposed. the hazardous constituents and any mismanagement. For example, many of We set out below general observations degradation products the wastes examined in today’s proposal about some of our approaches to risk (261.11(a)(3)(iii), 261.11(a)(3)(iv), are regulated as characteristic waste, assessment. 261.11(a)(3)(v), and 261.11(a)(3)(vi)) and releases or disposal to the land are are all considered in our evaluation of addressed under the existing RCRA 2. Characteristic Hazardous Waste constituent mobility (e.g., leaching regulations. We did not find any We describe in Section a. below our from waste) and fate and transport evidence of actual damage cases. analysis for wastes which are ‘‘100% models we used to project potential We describe our decisions under 40 characteristic’’—wastes which all concentrations of the contaminants to CFR 261.11(a)(3) in more detail in the generators report as characteristic and which individuals might be exposed. sector-specific discussion in section which all generators appear to manage We considered two additional factors, III.F below, and in the background in compliance with applicable plausible mismanagement and other documents. Generally, we conducted hazardous waste regulations. We

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00009 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55692 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules describe our approach to wastes which questionnaires also showed that there above, this provision authorizes (but are occasionally characteristic—but are a number of wastes that exhibit does not require) EPA to list wastes that managed in compliance—in Section b. characteristics at some facilities, but not exhibit characteristics without the below. Finally, we discuss in Section c. others. Consistent with previous listing analysis required under 40 CFR one waste which appears to exhibit a decisions (see for example, the most 261.11(a)(3). We believe that characteristic frequently, but does not recent petroleum refining listing at 63 noncompliance is an appropriate reason appear to be managed in compliance FR 42137), we focused on the volumes to use this authority to list a with hazardous waste regulations. of waste that did not exhibit characteristic waste. a. Wastes consistently exhibiting characteristics in our listing evaluation. d. Non-characteristic wastes disposed characteristics. For wastes which these For wastestreams identified as of in hazardous waste units. We industries identified as characteristic exhibiting characteristics and identified nine wastes which do not and managed in compliance with apparently managed in compliance with appear to exhibit any characteristic, but hazardous waste regulations, we are applicable regulations, we relied on the which are disposed of in Subtitle C proposing to find that there is no ‘‘no plausible mismanagement’’ and management units. Four of these wastes ‘‘plausible mismanagement’’ scenario to ‘‘other regulations’’ analysis described are sent to combustion unit regulated evaluate for listing. (See 40 CFR above. A hypothetical example follows. under Subtitle C of RCRA. The 261.11(a)(3)(vii).) The Subtitle C rules If one facility generated 40 tons per year remaining 5 wastes are sent to Subtitle applying to characteristic wastes of a properly-managed characteristic C landfills. We found that all of these adequately protect human health and waste, and a second facility generated wastes receive some treatment before the environment, especially where 60 tons per year of a non-characteristic land disposal. In one case available data waste generators are complying with waste, we would not evaluate the total indicates that the waste meets them. 40 CFR 261.11(a)(3)(x) authorizes of 100 tons of waste under a single applicable LDR treatment standards as us to consider actions taken by other approach. Rather, we would evaluate generated. regulatory programs. We believe we can the characteristic waste under the In general, these wastes have very reasonably interpret this to include the approach described above. For the waste limited potential for mismanagement rules for characteristic wastes under that did not exhibit a characteristic, we under 40 CFR 261.11(a)(3)(vii). This is Subtitle C . would conduct the type of risk particularly true for wastes which We acknowledge that the regulation of assessment described below in section generators place in on-site, Subtitle C characteristic wastes differs in some III.E. units with ample capacity. Also, in ways from the regulation of listed some cases, some of the wastes are wastes. For example, for characteristic c. Characteristic wastes not managed generated in very small quantities (less wastes, residues from treatment in compliance with Subtitle C. In one than 1 metric ton per year). These required by the land disposal case, we found a characteristic waste wastes are distinguishable from a non- restrictions need not always be placed where we believe that existing Subtitle characteristic organobromine waste sent in hazardous waste disposal units. C rules do not adequately prevent to a hazardous waste unit that we However, we do not regard the mismanagement. Four facilities generate decided to list in 1998. That waste had differences as ‘‘mismanagement.’’ a baghouse filter waste from the extremely high concentrations of a Rather, we believe that both approaches production of antimony oxide. Data constituent posing significant risks, and protect human health and the from our sampling and analysis at 2 received no treatment (see May 4, 1998; environment. Consequently, for the facilities showed exceedences of the 63 FR 24596).3 We request comment on purposes of this rule we decided that we toxicity characteristic. Two facilities the individual rationales set out in the would not propose to list a ‘‘100% recycle these wastes in a manner that sector-specific discussions and the characteristic’’ waste unless we found may comply with applicable background documents. evidence of extraordinary risks under regulations. Two other facilities, 3. Evaluations of Particular Units and one or more of the other factors in 40 however, did not identify their waste as Pathways of Release CFR 261.11(a)(3). characteristic wastes, and appear to For a few of the 100% characteristic manage them in ways which do not We are proposing to find that some wastes in this rule, we found factors comply with Subtitle C rules. Because of pathways of release from some units warranting further consideration. For this apparent noncompliance, we present low risks because they are example, we found that the sole concluded that it would be appropriate adequately controlled under other generator of cadmium pigment wastes to disregard the characteristic rules in Federal environmental regulations that codes them as hazardous, arranges for an analysis of the factors in 40 CFR minimize the likelihood of releases. We treatment to comply with the land 261.(a)(3). However, we also concluded are also proposing to find that other risk disposal restrictions, and then disposes that it was not necessary to conduct pathways present low risks due to of treated residues in a Subtitle D such an analysis. Since this waste fails physical or chemical attributes of the landfill. At the same time, we found that the toxicity characteristic, it clearly wastes. In some cases, we evaluated all the waste contains very high levels of contains levels of constituents which release pathways at a single unit under cadmium. We decided to investigate could pose threats to human health via a combination of these approaches. further to ensure that the treatment groundwater when placed in a a. Wastewater management. Facilities residues did not present significant municipal landfill, if leachate were to in these industries generally treat risks. We examined data relating to the migrate to a drinking water well at wastewaters in on-site wastewater treatment process and leachate sufficient concentrations. Since the treatment plants and discharge to monitoring data from the landfill generators are not managing the wastes surface waters, or pretreat the waste and receiving the residues. Based on these in compliance with applicable Subtitle discharge to an off-site wastewater data, we concluded that the residues did C regulations, we assume that this type not pose risks warranting listing. of mismanagement could occur at other 3 On April 9, 1999, the D.C. Circuit in Great Lakes Chemical Corporation v. EPA ordered that the b. Wastes which sometimes exhibit sites. Accordingly, we exercised our organobromine listing determinations be vacated. characteristics. Information submitted authority to propose to list this waste Accordingly, EPA removed the listings from CFR in responses to the Section 3007 under 40 CFR 261.11(a)(1). As noted (see 65 FR 14472: March 17, 2000).

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00010 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules 55693 treatment facility, e.g., a Publicly wastewaters in impoundments as part of process where we compared the total Owned Treatment Works (POTW). the MACT rulemaking. Therefore, we concentrations of the constituents of Under the Clean Water Act (CWA), did not do any further evaluation of concern to a series of soil screening discharges to surface waters are these emissions as part of today’s listing levels (see section III.E.3). controlled under the National Pollutant determination. We assessed the 4. Evaluation of Secondary Materials Discharge Elimination System (NPDES) potential for groundwater releases from and require an NPDES permit, while the impoundments. RCRA gives EPA jurisdiction only discharges to a POTW are subject to For sectors and wastes where facilities over materials that are discarded. EPA’s State and national pretreatment did not use surface impoundments for current definition of discard is set out standards.4 Point source discharges for wastewater management, we in the definition of solid waste at 40 the various sectors in the inorganics determined that ‘‘plausible CFR 261.2. Under this approach, listing are regulated under the CWA by mismanagement’’ would be continued process residuals (or ‘‘secondary the effluent guidelines and pretreatment management in existing tank-based materials’’) destined for recycling are standards in 40 CFR Parts 415 treatment systems. We do not view solid wastes within our jurisdiction if (Inorganic chemical manufacturing) and abandonment of existing treatment the recycling closely resembles waste 422 (Phosphate manufacturing). systems for surface impoundments as management. Conversely, if the Therefore, we did not evaluate NPDES ‘‘plausible,’’ because the manufacturers materials are recycled as part of an effluent or discharges to POTWs in have already made a considerable ongoing manufacturing process, they are today’s proposal. This approach is investment in wastewater treatment not solid wastes. The existing rules consistent with other listing rules. See, systems using tanks and will continue specifically exclude secondary materials for example, 60 FR 57759 (November to use them. Further, we assumed that from jurisdiction that are used directly 20, 1995, petroleum refining wastes wastewater treatment tanks retain (without reclamation), as ingredients in proposal). In a few cases, facilities sufficient structural integrity to prevent manufacturing processes to make new reported disposal of wastewaters by wastewater releases to the subsurface products, used directly as effective deep well injection in a permitted Class (and therefore to groundwater), and that substitutes for commercial products, or I UIC hazardous waste . In overflow and spill controls prevent returned directly to the original process these cases, the wells were units significant wastewater releases. Thus, from which they are generated as a regulated by the Underground Injection based on the lack of any significant substitute for raw material feedstock. 40 Control (UIC) program under the Safe likelihood of release of the constituents CFR 261.2(e). In addition, the existing Drinking Water Act (40 CFR Part 144). to groundwater, we did not project rules allow for closed loop reclamation These wells also had no migration significant risks to groundwater from where secondary materials can be exemptions under Section 148.20 to these wastes in the tank-based reclaimed and returned to the original allow disposal of untreated hazardous wastewater treatment scenario. We did production process provided that the waste. Therefore, we did not evaluate not model any releases to groundwater entire process is closed, the reclamation this scenario further. from tanks. This is consistent with our does not involve controlled flame For surface impoundments, we approach in other listing rules (see, for combustion, and the reclaimed material concluded that releases to air were not example, the proposed rule for is not used to produce a fuel or a likely to present concerns. For most chlorinated aliphatics production material that is used in a manner sectors, the constituents of concern are wastes at 64 FR 46476; August 25, constituting disposal. (40 CFR nonvolatile metals, and this makes 1999). We also considered the 261.4(a)(8)) As discussed in the January volatilization a highly unlikely pathway possibility of air releases from tanks. For 4, 1985, rulemaking, these are activities for constituents from normal wastewater most wastes, the constituents of concern which, as a general matter, resemble treatment practices. We recognize that are nonvolatile metals, making ongoing manufacturing operations more releases of volatile organic chemicals volatilization a very unlikely pathway of than conventional waste management from impoundments may be a potential release from tanks. For the hydrogen and so are more appropriately classified route of concern for one sector, cyanide sector, where volatile as not involving solid wastes. However, inorganic hydrogen cyanide production. compounds are likely and tanks are materials which would otherwise EPA is developing maximum achievable used in wastewater treatment systems, qualify for exclusion under these control technology (MACT) standards the tanks will also be covered by other provisions are not excluded if EPA finds for cyanide manufacturing under the CAA regulations as described above. In that the recycling is not legitimate. EPA Clean Air Act (CAA), which may addition, in many cases facilities have considers a variety of economic and address these emissions.5 EPA is installed tank covers, further reducing chemical factors when it determines evaluating possible air releases from the likelihood of release to the air. As whether or not a specific recycling a result, we have not modeled releases practice is legitimate. (See 4 In fact, 40 CFR 261.4 excludes ‘‘any mixture of to air from tanks for any wastes in this Memorandum from Sylvia K. Lowrance, domestic and other wastes that passes listing determination. Director Office of Solid Waste, through a sewer system to a POTW for treatment’’ b. Waste solids management. We concerning F006 Recycling, dated April (40 CFR 261.4(a)(1)(ii), and industrial wastewater 26, 1989). These determinations are very discharges that are point source discharges subject concluded that we did not need to to regulation under Section 402 of the CWA (40 model any releases of volatile site-specific and tend to be very time CFR 261.4(a)(2)). constituents from solids for the same consuming. EPA typically makes them 5 Clean Air Act—Title III: Upcoming MACT reasons set out above. The management in the context of site-specific Standards—Cyanide Chemical Manufacturing; practices of concern for waste solids enforcement or permitting actions. Unified Air Toxics Website: http://www.epa.gov/ ttn/uatw/mactupd.html: The hydrogen cynaide were landfills, including disposal in on- The existing rules, however, do not industry would also be subject to regulations under site and off-site landfills, and in a few exclude materials that are either 40 CFR Part 60, Subpart YYY under the CAA for cases, waste piles. We evaluated the contained in or used to produce fuels or volatile organic compound (VOC) emissions from potential for groundwater releases from that are directly used, or incorporated wastewater treatment at facilities in the synthetic organic chemical manufacturing industry (SOCMI), all landfills and piles. We also into a product that is used, in a manner which was proposed September 19, 1994 (59 FR considered the possibility of releases of constituting disposal. EPA asserts RCRA 46780). airborne particulates by a multistep jurisdiction for these types of use/reuse

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00011 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55694 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules circumstances as they more closely barriers to releases to the environment. the materials to an antimony oxide resemble conventional waste Where we found such management smelter located within the U.S. management rather than ongoing practices, we determined that there was For purposes of convenience, in the manufacturing. (See 50 FR 637–640, no significant potential for releases. We sector specific discussions below (and January 4, 1985). then evaluated the potential for releases in the various background documents) A series of court decisions also from the consent decree process itself. we describe all of the residuals as address the issue of our jurisdiction We found that the only points at which wastes. We emphasize, however, that over recycled materials. In general, they releases were expected were either those we have not determined whether any of hold that EPA lacks authority to regulate where we were already evaluating solid the residuals that are recycled are solid materials that are immediately reused in wastes for the purposes of this listing or wastes as defined in 40 CFR 260.2. We an ongoing manufacturing or industrial points where the facility released believe it is more appropriate to leave process. American Mining Congress v. uncontained gases outside of RCRA such site-specific determinations to EPA (824 F. 2d 1177 (D.C. Cir. 1987) jurisdiction. Consequently, we felt that other decision-making processes. (AMC I)); American Mining Congress v. we were evaluating all of the potential EPA (907 F. 2d 1179, 1186 (D.C. Cir. risks (within our jurisdiction) associated E. Description of Risk Assessment 1990) (AMC II)); American Petroleum with the recycling of these materials. In Approaches Institute v. EPA (216 F. 3d 50 (D.C. Cir. the antimony oxide sector, however, we 2000)). The most recent decision, found one residual that was being held Before turning to the details of the Association of Battery Recyclers, Inc. v. in containers for several years for risk assessment approaches used, we EPA (208 F. 3d 1047 (D.C. Cir 2000)), potential reuse. Our rules identify this want to highlight two general issues. remanded a rule regulating the reuse of practice as ‘‘speculative accumulation’’ First, we note that for this proposal we some closely related materials. We are and classify the materials held in such used a variety of screening still evaluating the impacts of this a manner as solid wastes. Accordingly, methodologies to assess a large number decision. However, the remand does not we assessed the risks posed by these of wastes. Due to time constraints affect this rule because we are not accumulated wastes. imposed by the consent decree relying on the exemptions in the We found that a few materials are schedule, we chose —where remanded rule.6 inserted into separate manufacturing appropriate— to use these For almost all of the residual processes co-located on-site with methodologies rather than conducting materials from these manufacturing consent decree processes. We evaluated more time-consuming, full-scale, risk processes which are re-used or recycled the potential for releases prior to assessment modeling. In general, in some way, we decided not to attempt reinsertion into that separate process. however, we believe that these to determine whether the recycling However, as explained above in section screening methodologies conservatively practice is not subject to regulation III.B, we did not evaluate any risks assessed risks, so that wastes that we under the court decisions and posed by use of residuals in processes ‘‘screened out’’ are unlikely to present regulations described above. Such that are not subject to our consent significant risks. determinations can be very time- decree deadline. Second, we want to describe our consuming, particularly where we find We also considered the risks of selection of plausible mismanagement recycling practices that appear not to be materials recycled off-site. We practices for both screening and full regulated, and then need to determine considered the potential for release modeling assessments. In general, we whether or not such practices are before the materials were transferred off- assessed the types of management units legitimate. Consequently, we decided site. We did not assess the off-site uses which, according to data available to us, that it would be more efficient to which involved non-consent decree facilities have actually used or examine first the potential risks posed manufacturing processes. In a few cases, contemplated using. Frequently, we by the reported recycling practices. If however, we found that the reuse found that facilities had made economic we found no significant risks, we would involved land placement or burning for investments that would make them decide not to list the material. If, on the energy recovery. These activities are likely to continue to use the same types other hand, we found risks, we evaluate always regulated as waste management of units. For example, where facilities the recycling practice prior to making a under the rules and court decisions had paid to install tanks to store or treat listing decision. described above. In those cases, we wastes, we assumed that they would To assess the risks of materials concluded that the materials were continue to use tanks rather than place recycled on-site by reusing them in one wastes from the consent decree process wastes in pits or surface impoundments. of the consent decree manufacturing where they were generated, and we Furthermore, we found that some waste processes, we first evaluated the evaluated risks posed by the use. For quantities were so large that it would be management of the materials prior to example, we evaluated the risks posed their re-use. We looked for closed by use of residual materials from the prohibitively expensive to transport piping, covers on containers, or similar production of boric acid as fuels for wastes off-site. Similarly, where cement kilns. In one case involving facilities had installed piping to return 6 On May 26, 1998, we promulgated a conditional antimony oxide residuals, we found that residual materials to their production exclusion from the definition of solid waste for the residuals were sent off-site to processes, we assumed that they would secondary materials (other than listed wastes) another smelter producing antimony continue to use these systems to recycle generated within the primary mineral processing those residuals. We also assumed that industry from which minerals, acids, cyanide, oxide. This smelter happens to be water, or other values are recovered by mineral located outside of the country. We did such facilities had found it more processing, with certain provisions. Because this not evaluate risks from its residuals, as economical to return those residuals to conditional exclusion only applied to non-listed their processes, and were thus not likely wastes, and we were making listing determinations, we have no legal jurisdiction to regulate we did not use this exclusion as a basis to not them. We have evaluated the production to send them to landfills or other types evaluate wastes for listing purposes. On April 21, of antimony oxide within the U.S. in of disposal units. 2000, the D.C. Circuit Court issued a decision this rulemaking, so we have evaluated We seek comment on all data, vacating a portion of this conditional exclusion. [See Association of Battery Recyclers, Inc. v. EPA. the risks that would be posed if this assumptions and methodologies used in 208 F.3d 1047 (D.C. Cir. 2000)]. generator changed its practice and sent our risk assessment for this proposal.

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1. What Risk Thresholds Were Used? hazard quotient (HQ) of one (1) solution which mimics acid rain, while EPA’s listing program generally indicates that the estimated dose is the TCLP uses a leach solution which defines risk levels of concern for equal to the reference dose (RfD) and, mimics acids formed in municipal carcinogens as risks within or above a therefore an HQ of 1 is EPA’s threshold landfills. In past actions, EPA has range of 1×10-6 to 1×10-4 (from 1 in of concern for non-cancer effects. recognized that the TCLP’s use of 1,000,000 to 1 in 10,000) at the upper Usually, doses less than the RfD (HQ<1) organic acids may not be appropriate for end of the risk distribution (e.g., 90th or are not likely to be associated with disposal scenarios that do not involve 95th percentile risk for a particular adverse health risks and, therefore, are municipal landfills. For example, in the exposure scenario). The level of concern less likely to be of regulatory concern. proposed rule for management and for non-cancer effects is generally As the frequency and/or magnitude of disposal of lead-based paint debris, EPA indicated by a hazard quotient (HQ) of the exposures exceeding the RfD used the SPLP to assess leaching from 1 or greater at the upper end of the increase (HQ>1), the probability of landfills that do not accept municipal distribution. Consistent with the listing adverse effects in a human population wastes (see 63 FR 70189; December 18, policy described in the dyes and increases. However, it should not be 1998). Similarly, EPA utilized the SPLP pigments proposal (59 FR 66075–66078) categorically concluded that all doses in screening low hazard wastes as part we used a 1×10-5 risk level and/or HQs below the RfD are ‘‘acceptable’’ (or will of its 1989 Bevill determination (see 54 of one to identify which wastes are be risk-free) and that all doses in excess FR 36592; September 1, 1989). of the RfD are ‘‘unacceptable’’ (or will In the context of EPA’s more recent candidates for listing. To make a listing result in adverse effects). mineral processing sector actions, we determination, we then used a weight- The values of the CSF and RfD that considered the relative merits of both of-evidence approach that considers the we use for assessing risks are generally the TCLP and the SPLP for various risk estimates along with other taken from EPA’s on-line toxicity data wastes in the mineral processing information related to the factors base called IRIS. However, in some industries; EPA decided to continue to described in 40 CFR 261.11(a)(3). For cases we used EPA’s compilation of rely on the TCLP for defining cancer, a risk threshold of one in toxicity benchmarks known as HEAST characteristically hazardous Bevill 1,000,000 represents the probability that or other sources, such as toxicological wastes, in part because we found that an individual will develop cancer over issue papers prepared by EPA’s National disposal in municipal landfills did a lifetime as a result of exposure to a Center for Environmental Assessment occur for some sectors. See the Land chemical contaminant. When we (NCEA).7 Disposal Restrictions Phase IV Final estimate the lifetime excess cancer risk, Rule at 63 FR 28598 (May 26, 1998). For 2. What Leaching Procedures Were we use an upper bound estimate of the today’s rule, however, we have specific Used? carcinogenic slope factor (CSF) as data showing that some wastes do not derived from laboratory studies in As noted in III.C, we used the TCLP go to municipal landfills and are animals or from human epidemiological and SPLP leaching procedures to unlikely to be disposed of in municipal studies. In addition, because the CSF evaluate the wastes in today’s rule. EPA landfills. We used the SPLP sampling typically relies on a number of developed the TCLP as a tool to predict results for wastes that were not likely to extrapolations (e.g., from animals to the leaching of constituents from the go to municipal landfills, and we used humans and from high doses to low waste in a the TCLP results for wastes going to doses) there is some uncertainty in the landfill, and the TC regulations use this municipal landfills. value of the CSF. method to determine if a waste is For non-cancer effects, which include hazardous under 261.24 (see the 3. How Were Wastes Screened To a wide variety of health effects, we used Toxicity Characteristic rule, 55 FR Determine If Further Assessment Was EPA’s reference dose (RfD) as a risk 46369; November 2, 1990). We have also Needed? threshold. A reference dose is an used the TCLP in the listing program to We used a number of approaches to estimate of an oral exposure that is estimate leaching concentrations for use eliminate from further consideration likely to be without an appreciable risk in groundwater modeling (for example, those wastes that could not plausibly of adverse effects in the general see the recent petroleum listing, 63 FR pose unacceptable risks. This served to population, including sensitive 42110, August 6, 1998). We believe the identify those wastes and chemical individuals, over a lifetime. The RfD can TCLP is the most appropriate leaching constituents that required further be derived from a NOAEL, LOAEL, or procedure to use for wastes in assessment. Different screening benchmark dose. Uncertainty factors are municipal landfills, because the approaches were used depending on the applied to address limitations of the leaching solution is similar to the type type of waste management practices available toxicological data and are of leachate generated from the employed in the industry and, in some necessary to ensure the RfD is protective decomposition of municipal waste. The instances, the waste volume and the of individuals in the general population. TCLP leaching solution is a solution location of the waste management units. The use of uncertainty factors is based containing acetic acid that is adjusted to For wastes that are managed in on long-standing scientific practice. a pH of 4.93 or 2.88, depending on the landfills, groundwater contamination is Uncertainty factors when combined acidity of the waste sample. the primary source of human exposures, commonly range from 10 to 1000 EPA developed the SPLP as a method particularly for certain metals and other depending on the nature and quality of to predict leaching from wastes or soils inorganic compounds that are the underlying data. The RfD under exposure to the slightly acidic, nonvolatile, such as those present in the methodology is expected to have an dilute solution generated by normal wastes that are the subject of today’s uncertainty spanning perhaps an order rainfall. The SPLP test uses a leach rule. We compared leachate of magnitude. To assess risks associated concentrations derived from the TCLP with non-cancer effects, we used a 7 EPA’s Integrated Risk Information System (IRIS) or SPLP test measurements to levels in hazard quotient (HQ), which is defined may be found at http://www.epa.gov/iris. See also drinking water that are protective of ‘‘Risk Assessment for the Listing Determinations for as the ratio of the estimated dose of a Inorganic Chemical Manufacturing Wastes’’ (August human health. These levels, referred to given chemical to an individual to the 2000) for a discussion of the toxicity benchmark as health-based levels (HBLs), are reference dose for that chemical. A values used in today’s rule. designed to be protective of both

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00013 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55696 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules children and adults. Health-based levels plausibly pose a risk to human health available data.10 If the waste (HBLs) are levels in environmental when disposed of in a landfill. concentrations exceeded background media that would not exceed EPA’s risk Typically wastes generated in volumes levels in soils, we performed a second thresholds given conservative of less than 1 or 2 metric tons per year level screen by comparing the waste assumptions regarding exposure (e.g., a were considered as candidates for this concentrations with soil ingestion HBLs. level in drinking water that would not de minimis analysis. This analysis Soil ingestion HBLs assume direct exceed a risk threshold for an individual assumed that the entire mass of the contact with the waste and, therefore, whose drinking water intake was at the chemical contaminant in a volume of are more conservative than HBLs based high end of the distribution for the waste that is generated in a year’s time on inhalation exposures. In those general population).8 Although an HBLs would leach out of the waste and instances when the waste represents a concentration level at the infiltrate into groundwater in the same concentrations exceeded both point of exposure, we conservatively year. The only dilution that was background levels and soil ingestion assumed direct contact with the wastes assumed to occur was with the volume HBLs, we performed a third level screen (i.e., no dilution) for the purpose of of water that infiltrated into the landfill. using the results of EPA’s air screening out wastes and chemical To minimize the amount of dilution we characteristics study. This study constituents that could not pose chose a conservative infiltration rate developed levels of chemical unacceptable risks and, therefore, do not based on the infiltration that could contaminants in wastes that are merit further analysis. As explained occur for a relatively low permeability protective of human health with respect previously, we used SPLP soil underlying a relatively small to inhalation exposures when managed measurements for wastes that are landfill (corresponding to the 10th in a variety of ways.11 In particular, air managed in landfills containing only percentile of the distribution of characteristic levels were developed for industrial wastes and TCLP municipal landfill areas nationwide). waste piles at several different distances measurements for wastes that are However, in some cases the resulting from a potential receptor. We used the managed in landfills which also contain infiltration was less than the amount of air characteristic levels corresponding to municipal wastes. For wastewaters that water that would be withdrawn from a a downwind distance of 25 or 150 are managed in surface impoundments, well by a household for domestic usage. meters (80 or 500 feet). Because the air we used the concentration in the filtered In these instances, we diluted the characteristic levels include the effect of liquid (i.e., the SPLP filtrate) because infiltrate into the minimum volume of atmospheric dilution, they are the filtrate is more representative of the water needed to support a household significantly higher than soil ingestion fraction of the waste that could infiltrate well, which we estimated from data on HBLs. In most cases waste into the subsurface environment. U.S. per capita water consumption concentrations are either below Regardless of the type of measurement, assuming a family of four. The background or below soil ingestion if the result of the chemical analysis for concentration derived using this HBLs for the wastes EPA evaluated. a particular compound was below the procedure was then compared to the Moreover, we found no instances in limit of detection but the compound HBLs. Any chemical contaminant that which air characteristic levels are was detected in the waste, then we used did not screen out as a result of this exceeded. In the cases where waste 1⁄2 the value reported by the laboratory analysis we identified as a constituent concentrations exceeded the soil as the limit of detection for that of concern (CoC) requiring further compound. Any chemical contaminant ingestion levels, the exceedence was assessment. While we do expect the de typically less than a factor of 2 to 3. We in a waste that did not screen out minimis screen to be conservative against HBLs (i.e., the waste believe it is highly unlikely that off-site overall, the degree to which it is exceedences due to windblown dust concentration was a factor of 2 or less conservative depends on many waste times the HBLs 9) we identified as a from piles or landfills would actually and site-specific factors. (For example, exceed the soil ingestion levels given constituent of concern (CoC) requiring our sampling and analysis data indicate further assessment. However, very low this low level of exceedence in the that in some cases essentially all of the waste. Therefore, we conclude that risks volume wastes were subject to further chemical constituent leached out of the screening, as described below. associated with particulates from piles sample over the duration of the leach For very low volume wastes that did and landfills transported by an air test.) not screen out against HBLs, we pathway are not significant and no performed an additional conservative For wastes managed in waste piles further assessment is needed. screen to determine if the waste could and landfills, we performed a multi- level screening analysis to determine if 10 Different statistics may be used for 8 Details on how HBLs are derived may be found further assessment of the air pathway characterizing background levels depending on the in the risk assessment background document for was needed. Wind blown dust from data available. The mathematical properties of the today’s proposal, ‘‘Risk Assessment for the Listing wastes managed in piles is a potential arithmetic mean allow it to be used when only average values rather than the original data are Determinations for Inorganic Chemical source of human exposures. This Manufacturing Wastes’’ (August 2000). available. However, if the original data are 9 We used professional judgment to screen out pathway is also possible for landfills, available, the data can be pooled and a geometric constituents with concentrations within a factor of but likely to result in much lower mean can be calculated. If the data are positively two of the HBLs. Historically, our models have releases due to the common usage of skewed, as is often the case, the arithmetic mean will be higher than the geometric mean. We suggested that the dilution and attenuation of daily and longer-term cover at landfills. constituents in the subsurface will generally result consider either statistic to be a central tendency in dilution and attenuation factors (DAFs) of 2 or In the first level screen we compared the measure of background levels. However, greater. (See, for example, the DAFs estimated for waste contaminant total concentrations background levels are highly variable and may be the petroleum refining listing determination, 63 FR to background levels in soils. considerably higher or lower than the national average at any given location. See, for example, the 42110, and the docket for today’s rulemaking for Background soil levels were taken from DAFs calculated to support today’s proposal.) If our U.S. Geological Survey paper ‘‘Elemental consideration of site-specific factors had indicated published compilations of levels in Concentrations in Soils and Other Surficial that a very low DAF were likely for actual exposure native soils nationwide and were Materials in the Conterminous United States,’’ (e.g. known drinking water wells placed very close generally characterized using a paper 1270, U.S. Government Printing Office, 1984. 11 to the management until boundary), we would have geometric mean or (in a few instances) See U.S. EPA, ‘‘Revised Risk Assessment for modeled that waste rather than screening it out the Air Characteristic Study,’’ Office of Solid Waste, using professional judgment. an arithmetic mean concentration of the EPA 530–R–99–019, November 1999.

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EPA derived HBLs for chemical have the potential to adversely impact defines high end as the 90th percentile contaminants from toxicity benchmarks surface waters before eliminating the and greater of the distribution of and a set of exposure assumptions that wastes from further consideration. We exposures in the population. Central differ depending on the type of health used EPA’s national water quality tendency generally refers to the mean or effect and exposure pathway. For criteria for this purpose. Specifically, 50th percentile of the distribution. carcinogenic effects, HBLs were derived we compared waste concentrations (i.e., Central tendency and high end from a cancer slope factor (CSF) for the SPLP measurements for wastes managed estimates may be generated using either oral route of exposure. For non-cancer in on-site landfills and SPLP filtrate probabilistic or deterministic effects, HBLs were derived from EPA’s measurements for wastes managed in approaches.14 oral reference dose (RfD) for the surface impoundments) directly to We evaluated potential groundwater compound. Risk thresholds were as ambient water quality criteria that have exposures over a 10,000 year time described previously. Drinking water been established for the protection of period. Evaluating peak doses over this and soil ingestion HBLs for individual both human health and aquatic life. Any time horizon allows the model to chemical contaminants are presented chemical contaminant in a waste capture the slow movement of some elsewhere.12 The exposure assumptions managed under these circumstances that chemicals through the subsurface. we used for deriving the HBLs are did not screen out against ambient water While exposure assumptions (e.g., land described as follows. quality criteria (within a factor of 2) we use patterns, climate, environmental For drinking water exposures, we identified as a constituent of concern and other exposure assumptions) are derived HBLs for carcinogenic effects (CoC) requiring further assessment. expected to change over 10,000 years, for an adult exposed for 30 years and EPA recently republished ambient such changes are difficult to predict. We having a tap water intake of 1.4 liters water quality criteria for a large number believe such a time period is per day. This represents 21 milliliters of chemical contaminants (see 63 FR appropriate to ensure human health is per day on a per kilogram body weight 68354; December 10, 1998). Separate protected. Even with long time periods, basis, which is the mean tap water criteria for the protection of aquatic life we are still concerned with the risk that intake for adults. A duration of exposure have been established for fresh water would result once contamination of 30 years represents the 95th and salt water. In a number of instances reaches potential drinking water wells. percentile of the distribution of waste management units are located Given that the metals of concern do not residential occupancy periods for adults adjacent to estuarine environments. In degrade in the environment, we believe nationwide. We derived HBLs for non- these cases, for screening purposes, we a long modeling time period is cancer effects for a child having a tap used the lower of the fresh water and necessary. Further, there is uncertainty water intake of 1.3 liters per day. This salt water criteria. in when peak concentrations at the represents 64 milliliters per day on a per receptor well may occur, and using the 4. How Was the Groundwater Pathway kilogram body weight basis and 10,000 year time frame makes it more Evaluated? corresponds to the 90th percentile of the likely that we will capture the peak risk distribution of tap water intakes in We conducted modeling analyses to in our evaluation. EPA has used similar children that are 1 to 10 years of age.13 assess possible risks to human health time horizons for groundwater modeling Because the drinking water HBLs from wastes managed in land-based in past hazardous waste rules. 15 incorporate conservative exposure units such as landfills and surface For modeling chemical concentrations assumptions, we consider them to be impoundments. We used fate and in ground water, many input parameters appropriate for screening purposes. transport models to estimate were varied. These included waste Soil ingestion HBLs were derived contaminant concentrations that might characterization data (e.g., chemical from either the CSF or the RfD assuming occur in a residential drinking water concentrations and waste volumes), a soil ingestion rate of 200 milligrams well from migration of uncontrolled waste management practices (e.g., waste per day and an exposure duration of 8 releases of leachate from a waste management unit size and infiltration years. A soil ingestion rate of 200 management unit through the rates), hydrogeological parameters (e.g., milligrams per day (about 3/100th of a subsurface environment. We assessed depth to water table, hydraulic teaspoon) is a conservative estimate of human exposures to these contaminants conductivity, and aquifer thickness), the mean intake rates for children in the from information on the amount of tap and chemical parameters (e.g., soil- age range of 1 to 7. An exposure water an individual drinks and the water partition coefficient). We duration of 8 years is an estimate of the length of time an individual might conducted extensive sensitivity analyses mean residential occupancy period for a reside at a residence and utilize water to determine which of these parameters 6 year old child. In selecting these from a residential well. We then had the greatest influence on the risk values for use in deriving soil ingestion assessed what the human health risks results. For a detailed discussion of the HBLs, we considered the likelihood that would be as a consequence of such ground water analysis, including children would actually come into exposures. parameter distributions, input direct contact with the wastes. We took a probabilistic approach to assumptions, and sensitivity analyses, In cases where wastes are known to be the assessment of human exposures. In see the risk assessment background managed in on-site landfills or surface this approach, we used Monte Carlo document for today’s proposal, ‘‘Risk impoundments that are located adjacent simulation techniques to determine the Assessment for the Listing to or in close proximity to surface distribution of groundwater Determinations for Inorganic Chemical waters, we used additional screening concentrations to which an individual Manufacturing Wastes’’ (August 2000). criteria to identify wastes that could could be exposed and combined this with distributional data for the general 14 We relied upon the probabilistic risk estimates 12 See the risk assessment background document population on the intake rates of tap for today’s proposal. However, both deterministic for today’s proposal, ‘‘Risk Assessment for the water and the duration of exposure. We and probabilistic approaches are presented in the Listing Determinations for Inorganic Chemical then assessed the risks to human health risk assessment background document. Manufacturing Wasters’’ (August 2000). 15 See HWIR proposal at 64 FR 63429, November 13 See EPA’s ‘‘Exposure Factors Handbook’’ (EPA/ from both the middle (central tendency) 19, 1999, and the final rule for the recent listing of 600/P–95/002Fa), August 1997, for additional and upper (high end) portions of the wastes from petroleum refining at 63 FR 42157, details on human exposure factors. distribution of human exposures. EPA August 6, 1998.

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In assessing groundwater exposures from the uppermost aquifer where and depends on the type for wastes managed in off-site landfills, contaminant concentrations are of soil and the climate where the we considered the locations of every expected to be the highest. landfill is located. For surface industrial and municipal landfill known Equilibrium sorption of chemical impoundments, the infiltration rate is to receive the wastes and the volume of contaminants onto soil and aquifer estimated from the liquid depth in the wastes managed at each of these sites. materials is parameterized in the impoundment and from the hydraulic In so doing, we considered only that EPACMTP model using a soil-water conductivities and thicknesses of the volume of waste that is currently not partition coefficient (Kd). For today’s sediments and the underlying soil. We being managed as hazardous waste. For proposed rule, we used values for Kd assumed that surface impoundments wastes managed on-site by multiple that have been derived from field have no liner or leachate collection facilities, we generally considered only studies and have been published in the system. Unconsolidated or loose those facilities where groundwater scientific literature. An empirical sediments are treated as free liquid so exposures are expected to be the distribution was used to characterize the that the pressure head on the highest. These locations were identified variability of Kd for chemical underlying, consolidated sediments is by considering the concentration levels contaminants for which sufficient determined by the depth of the liquid in of chemical constituents in the waste published data were available. However, the impoundment and the depth of the managed at the site and the proximity for several chemical contaminants unconsolidated sediments. As sediment of on-site waste management units, having relatively few published values accumulates at the base of the namely landfills and surface (e.g., antimony and thallium), a log impoundment, the weight of the liquid impoundments, to potential off-site uniform distribution was used.16 Our and upper sediments acts to compress receptors. Our rationale for selecting use of empirically derived partition (or consolidate) the lower sediments. particular locations for conducting coefficients assumes that sorption is The result is the formation of a modeling analyses is discussed in linear with respect to groundwater consolidated sediment layer having a section III.F for the specific inorganic concentration (i.e., the Kd isotherm is hydraulic conductivity that is much sectors. linear). However, sorption is not lower than the previously unconsolidated sediment. a. How were contaminant unlimited and will tend to level off as We assumed that landfills have an concentrations in groundwater groundwater concentrations increase operational life of 30 years.17 In modeled? For modeling fate and beyond the linear range (i.e., the Kd landfills, leaching of contaminants from transport in the subsurface isotherm becomes non-linear). This condition is most likely to occur in the the waste leads to an exponential environment, we used the groundwater decrease in the leachate concentration model EPACMTP (EPA’s Composite unsaturated zone where dilution is limited, if leachate concentrations are with time. The rate at which this occurs Model for Leachate Migration with depends on the volume of waste Transformation Products). The model sufficiently high. EPA has sometimes used the disposed of in the landfill and the total consists of two coupled modules: (1) A MINTEQA2 equilibrium speciation concentration of chemical contaminants one-dimensional module that simulates model to estimate Kd’s for a variety of in the waste. We used the measured infiltration and dissolved contaminant metals rather than relying solely on field TCLP concentration (for disposal in a transport through the unsaturated zone, measurements. However, recently a municipal landfill) or SPLP and (2) a three-dimensional saturated number of technical issues have been concentration (for disposal in an zone flow and transport module. Fate raised concerning the model and its industrial landfill) as the initial leachate and transport processes accounted for in application. EPA is in the process of concentration for modeling. In contrast, the model are advection, hydrodynamic evaluating the model to address those we assumed that surface impoundments dispersion, sorption equilibria, 18 issues. Therefore, we have decided not have an operational life of 50 years. hydrolysis, and dilution from recharge to use MINTEQA2 for today’s proposed Many surface impoundments are to the saturated zone. The model rule. Once the evaluation is completed periodically dredged and, therefore, can assumes that the soil and aquifer are and the issues are satisfactorily be maintained in service for longer uniform porous media. EPACMTP (as resolved, EPA may again choose to use periods of time. With surface used in this analysis) does not account the model in an appropriate form in impoundments, leachate concentrations for heterogeneity of the aquifer or for future rulemakings. are not expected to decrease over time preferential migration pathways such as Infiltration of leachate from landfills and, therefore, leachate concentrations fractures and macro-pores or for into the subsurface is modeled using the are assumed to remain constant during colloidal transport, any or all of which HELP model (Hydrologic Evaluation for their operational life. We used the total could be important at a particular site. Landfill Performance), a quasi-two- concentration of chemical contaminant Although EPACMTP simulates steady- dimensional hydrologic model used to measured in the wastewater or (for state groundwater flow in both the compute water balances for landfills. wastewaters with high levels of solids) unsaturated zone and the saturated We assumed that landfills have a final the concentration measured in the SPLP zone, the model (as used in this earthen cover but no liner or leachate filtrate as the leachate concentration for analysis) simulates contaminant collection system. The net infiltration modeling. transport from a finite source and rate that is calculated by the model The fate and transport simulation predicts the peak contaminant considers, among other factors, modules in EPACMTP are linked to a concentration arriving at a down- precipitation, evapotranspiration, and Monte Carlo module to allow gradient groundwater well. Only quantitative consideration of variability migration of chemical contaminants 16 A log uniform distribution is a distribution that within the surficial aquifer is modeled has equal probabilities at all percentiles when the 17 U.S. Environmental Protection Agency, ‘‘Draft by EPACMTP. We did not model parameter is transformed into logarithms. For these National Survey of Solid Waste (Municipal) migration of contaminants to deeper chemical constituents, we used a log uniform Landfill Facilities,’’ Office of Solid Waste, distribution that was centered on the geometric Washington, D.C., 1988 (EPA/530–SW–88–034). aquifers but, instead, based our mean of the available data and had a width of 3 18 See assumptions made for the recent proposed assessment on exposures that might logs. This was done to better account for the hazardous waste identification rule at 64 FR 63382; occur from groundwater withdrawn variability normally seen in measurements of Kd. November 19, 1999.

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00016 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules 55699 and uncertainty in groundwater determined by associating the site determine the closest point at which a concentrations due to variability and location with a soils classification residential well could be located and, uncertainty in model input parameters. region. We defined soil classification therefore, the point at which human We use a regional site-based regions from information on the soil exposures could plausibly occur. We methodology to associate the types found within a 100 mile radius of considered the location of the facility appropriate regional climatic and the site location. The distribution of soil property boundary, the type of land use hydrogeologic conditions to the location textures for the region was determined adjacent to the property boundary, the of actual waste management sites. This by identifying the soil texture presence of surface waters that could methodology accommodates classifications from data contained in intercept ground water flow, utilization dependencies between the various the U.S. Department of Agriculture of ground water for residential or model input parameters. In this (Natural Resources Conservation agriculture uses, and the existence of approach, a site location is assigned to Service) STATSGO (State Soil residential drinking water wells in the one of 13 hydrogeologic regions and one Geographic) data base. The predominant direction of ground water flow. For both of 97 climatic regions that are linked to soil textures within each mapping unit on-site and off-site waste management, databases of climatic and hydrogeologic (which represents a collection of soils) we assumed the receptor well was parameters. A climatic data set provides were identified and the fraction of the located down-gradient from the waste infiltration and recharge values for three three soil textures used in the management unit and that ground water soil textures at each of 97 climatic EPACMTP model were determined (i.e, is withdrawn from the top ten meters of centers in the contiguous United States. sandy loam, silt loam, and silty clay the aquifer and within the lateral extent The soil textures are based on a Soil loam). These soil classification regions of the contaminant plume. Exposures Conservation Service soil mapping were used for modeling off-site were further assumed to occur out to a database and U.S. Department of municipal and industrial landfill sites. distance of a mile from the waste Agriculture definitions of coarse, A similar approach was taken for on-site management unit. medium, and fine soil textures. (These landfills and surface impoundments Our assessment of human exposures textures are represented in EPACMTP except that the predominate soil did not consider naturally occurring by sandy loam, silt loam, and silty clay textures from mapping units that background levels in ground water. loam, respectively.) Infiltration rates for correspond to the site location itself Background levels in ground water are the waste management unit and the were identified. These were compared not a significant source of human recharge rate for the surrounding region for consistency with other soils exposure for several of the more were determined for each soil type and information available for the site. Once important chemical constituents in the climatic center using the HELP model. the fraction of the three soils textures is wastes that are the subject of today’s A site location is generally assigned to determined for a given site location, a proposal (e.g., antimony and thallium). the climatic center that is geographically distribution of soil parameter values is However, for manganese, dietary closest to the site. generated from information on the exposures are a significant source of Each site location is also located on a distribution of soil parameter values for background exposures. We did not groundwater resource map (from a U.S. the three soil textures and the fraction attempt to quantify the cumulative risks Geological Survey inventory of State of each soil texture for the site. These from both dietary and drinking water groundwater resource maps) and a parameters are used for modeling exposures combined and, therefore, this hydrogeologic region is assigned to the groundwater flow and contaminant is a source of uncertainty in our site based on the primary aquifer type transport in the unsaturated zone and assessment of risks from manganese in at that location. A hydrogeologic include saturated conductivity, these wastes. database provides a distribution of moisture retention properties, water Human exposures were characterized values for depth to groundwater, aquifer content, and organic matter content. in terms of lifetime average daily dose thickness, hydraulic gradient, and A full description of the groundwater (LADD) and average daily dose (ADD) hydraulic conductivity for each of 13 modeling analyses conducted for for both children and adults. We used hydrogeologic regions. The today’s proposed rule may be found in the LADD for assessing cancer risks and hydrogeologic data base (HGDB) was the background document, ‘‘Risk the ADD for assessing risks from non- developed from a survey of Assessment for the Listing cancer effects (including reproductive, hydrogeologic parameters for Determinations for Inorganic Chemical developmental, neurological, approximately 400 hazardous waste Manufacturing Wastes’’ (August, 2000). cardiovascular, hematologic, metabolic, sites nationwide. These site-specific b. How were human exposures and a wide variety of other physiologic data were then regrouped according to assessed? Our assessment of human effects). Exposures to children of age hydrogeologic classifications, and a exposures to contaminated ground one to six years and adults of age 20 to distribution of parameter values was water is based on a residential drinking 64 years were assessed. We used generated for each of the 13 water scenario. A different approach information from EPA’s Exposure hydrogeologic regions (made up of 12 was used for determining the location of Factors Handbook 20 to characterize tap specific hydrogeologic environments exposure depending on whether the water intake rates for individuals and and one miscellaneous category). In the wastes are managed on-site or are residential occupancy periods of analysis for today’s rule, we modified shipped off-site for disposal. For waste households (and, therefore, the length of the above approach for on-site waste shipped to off-site municipal landfills, time an individual could be exposed to management units to enable available we used EPA’s National Survey of contaminated ground water). site-specific information on depth to Municipal Landfills 19 to determine the Distributional data on tap water intake groundwater to be used in place of the distance from the landfill to the receptor rates for individuals and residential values found in the database. well. We also used these same data for occupancy periods for households were We also used a regional site-based off-site industrial landfills. For wastes methodology to associate the managed on-site in either landfills or 20 U.S. Environmental Protection Agency, appropriate soil characteristics to a ‘‘Exposure Factors handbook’’, Volumes I and III, surface impoundments, we attempted to Office of Research and Development, National given site location. In this approach, a Center for Enironmental Assessment, Washington, distribution of soil textures at a site is 19 Ibid. DC., August 1997 (EPA/600/P–95/002Fa and c).

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00017 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55700 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules used to generate both the ADD and be intercepted by surface water. Because recommends the long-term harmonic LADD exposure estimates. For assessing this is a screening analysis, we made mean be used as the design flow.23 The lifetime exposures, we averaged the well conservative assumptions that are likely harmonic mean is always less than the water concentrations over the duration to overstate the infiltration of leachate arithmetic mean and is used in place of of exposure (i.e., the residential and, therefore, the potential release to it because low flow conditions drive occupancy period). We also averaged surface water. For example, for on-site long-term average water quality. the tap water intake rates over the landfills, we assumed a soil type (sandy However, because this flow statistic was duration of exposure to account for the loam) that is likely to overstate the not available, we estimated the changes in tap water intake rates with infiltration rate even in the absence of harmonic mean flow from the arithmetic age that are seen among children. For liners or leachate collection systems. mean flow and the 7Q10. estimating the ADD, we used the peak Similarly, for surface impoundments we As a result of the screening level 9-year average well water concentration assumed a sludge thickness (8 inches) analysis, all wastes screened out for but did not further average the and soil type (sandy loam) that is likely which the ground water to surface water estimated exposure (which we believe to overstate the infiltration rate. In pathway was a concern. Therefore, no would be inappropriate given the range addition, we assumed no retardation in additional analysis of this pathway was of possible health effects we want to the migration of chemical contaminants conducted. protect against). Previous work with the in ground water due to sorption or other 6. What Are the Limitations and EPACMTP ground water model has processes. shown that the peak 9-year Due to the nature of these releases, Uncertainties of the Assessment? concentration and the maximum which are likely to occur over a wide Our assessment of exposures and risks predicted concentration are nearly area, we assumed that the inflow of is subject to a variety of limitations and identical. contaminated ground water was rapidly uncertainties. These are discussed in A full description of the methods and diluted into surface water and that there some detail in the background data used in the exposure assessment was little or no mixing zone. We document for today’s proposed rule. A for today’s proposed rule may be found followed EPA’s Office of Water number of these are highlighted here. in the background document, ‘‘Risk guidance for determining the design We assumed our sampling and Assessment for the Listing flows for rivers as regards water quality analysis data are fully representative of Determinations for Inorganic Chemical criteria. The appropriate design flow the range of wastes generated in the Manufacturing Wastes’’ (August, 2000). depends on the particular water quality effected industries. However, our own 5. How Was the Surface Water Pathway impact being evaluated. For assessing data show that there are significant Evaluated? potential impacts on aquatic life, we variations in waste concentrations used the ‘‘7Q10’’ as the design flow. The across facilities in a given industry. A number of facilities that generate 7Q10 is the seven day low flow with a Variability in waste concentration that wastes covered by today’s proposed rule return frequency of once every 10 years is unaccounted for could lead to an are located adjacent to rivers or bays. As and is the recommended design flow for over- or under-estimation of risks. a consequence, the potential exists for use with chronic water quality criteria However, any tendency toward under- subsurface releases of chemical for the protection of aquatic life. We estimation is likely to be mitigated to contaminants from on-site management believe that chronic water quality some extent by our selection of wastes of the wastes to enter these river and criteria are the appropriate criteria for and exposure scenarios that are bay systems through ground water evaluating the potential impact of intended to capture the highest risks. inflow. In instances where no direct continuing steady releases, such as We also assumed that our methods for contact with ground water is likely to those that would result from subsurface measuring the leaching behavior of occur (as there would otherwise be if, discharge of contaminated ground wastes (i.e., the TCLP and SPLP test for example, ground water was being water. On the other hand, EPA generally procedures) are both representative of used for residential drinking water), it uses the ‘‘30Q5’’ as the design flow for the range of leaching conditions that becomes important to evaluate the assessing potential impacts on human exist under real world conditions and potential water quality impacts of these health. The 30Q5 is the thirty day low accurately quantify the concentrations releases on surface waters in the context of contaminants that leach into the of hazardous waste listings. However, flow with a return frequency of once every 5 years and is the recommended subsurface environment from a given we wish to emphasize that the surface waste management unit. However, we water impacts considered in today’s design flow for use with water quality criteria for the protection of human know that many metals exhibit varying proposed rule are due to subsurface (or amphoteric) behavior with respect to releases to ground water only. Direct health as regards non-cancer effects. pH and that any one test procedure is discharges to surface waters are already However, a 30Q5 design flow was not capable of characterizing leaching regulated by the Clean Water Act under available in all cases. In these instances, behavior only under a particular set of the NPDES permit system and are not we estimated the 30Q5 based on the 7Q10 design flow.22 For carcinogens conditions. considered further in today’s The ground water model we used in proposal.21 (e.g., arsenic), lifetime exposures are the our analysis (i.e., EPACMTP) is We conducted a screening level primary concern and a design flow that designed to characterize dilution and analysis to evaluate potential surface corresponds to a longer averaging time water impacts. In this analysis, we is appropriate. For this reason, EPA attenuation in the subsurface estimated the volume of leachate that environment under homogeneous would infiltrate into ground water and 22 EPA guidance provides a simple rule of thumb conditions. The model does not account assumed that this entire volume would for estimating the 30Q5 from the 7Q10 depending for subsurface heterogeneities, nor does on the size of the river. For smaller rivers (defined it account for fractured flow or colloidal as those with a low flow of 50 cfs or less), the 30Q5 21 Industrial wastewater discharges that are is 1.1 times the 7Q10. For larger rivers (low flow transport. These conditions, if present at regulated under the National Pollutant Discharge of 600 cfs or greater), the 30Q5 is 1.4 times the Elimination System (NPDES) Permit Program are 7Q10. See ‘‘Technical Support Document for Water 23 The harmonic mean is defind as the inverse of specifically excluded from regulation as hazardous Quality-Based Toxics Control,’’ EPA/505/2–90–001, the average of the sum of the inverses of the wastes under 40 CFR 261.4(a)(2). March 1991. recorded flows.

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00018 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules 55701 a site, can lead to less dilution and considerable uncertainty) may have an titanium dioxide pigments and attenuation of contaminant levels than impact on the estimated risks and, chromate pigment. predicted by the model, causing ground therefore, the outcome of the risk The manufacturers use two different water concentrations to be under assessment. processes to produce antimony oxide. In estimated. In addition, sorption of metal Other important uncertainties include the first process, antimony metal is species onto soil and aquifer materials those related to the health effects of roasted in the presence of air. The exhibits considerable variability chemical contaminants in humans antimony oxide forms as a fume, cools depending on geochemical conditions (hazard identification), absorption and and condenses in a baghouse. In the and the total concentration of the metal metabolism of ingested contaminates second process, crude (low grade) present at a given location. Although (pharmacokinetics), and biological antimony oxide is roasted in the our use of empirically derived Kd response (dose-response relationships). presence of air to produce higher grade values captures some of this variability, These and other limitations and antimony oxide. The antimony oxide the available published data are fairly uncertainties are discussed in the cools and condenses in a baghouse. The limited for certain metals (e.g., background document, ‘‘Risk crude antimony oxide comes either from antimony). We have accounted for the Assessment for the Listing off-site or is recycled from within the uncertainty associated with the small Determinations for Inorganic Chemical facility. number of data points explicitly for Manufacturing Wastes’’ (August, 2000). c. How does the Bevill Exclusion these metals by expanding the range of F. Sector-Specific Listing Determination apply to wastes from the antimony Kd values used for modeling (to three Rationales oxide manufacturing processes? orders of magnitude). Even for metals Antimony oxide producers use a range that have abundant data (e.g., arsenic), We seek comments on all proposed of raw materials to produce antimony it is unlikely that the range of variability listing decisions in this section, and the oxide, including antimony metal ingots, apparent in the data could exist at a underlying rationales used to support sodium antimonate, and antimony ore given site. our proposals. concentrate, and some facilities have Uncertainty associated with the 1. Antimony Oxide claimed that wastes generated from the specification of Kd as noted above could production of antimony oxide are Bevill lead to an over- or under-estimation of a. Summary. We have evaluated exempt. Wastes generated from risk. However, a tendency toward over- antimony oxide production wastes and processes using either antimony ingots estimation is likely to be mitigated by propose to list two wastes from this or sodium antimonate (both of which the fact that under near steady-state process as hazardous: (1) Baghouse are saleable mineral products) are conditions (when ground water impacts filters and (2) slag that is disposed of or considered chemical manufacturing are the greatest), concentrations in speculatively accumulated. We propose wastes rather than mineral processing ground water are little influenced by to list the baghouse filter waste under wastes and are not eligible for the Bevill Kd. Under non-steady conditions, any the criterion in 40 CFR 261.11(a)(1) exemption. The September 1, 1989 tendency toward over- or under- because it routinely exhibits one or Bevill final rule states at 54 FR 36620– estimation is limited by the variability more of the characteristics of hazardous 21 that chemical manufacturing begins inherent in the empirical distributions waste, but the waste is not consistently if there is any further processing of of Kd used in the analysis, which managed in compliance with Subtitle C mineral product. include both relatively high and regulations. We propose to list the slag relatively low values of Kd. under the criteria in 40 CFR 261.11(a)(3) Two of the facilities also purchase an Nevertheless, in general the risk because of risks associated with land antimony ore concentrate as a raw estimates are sensitive to the disposal. material and place this material in kilns specification of Kd and, therefore, this K176 Baghouse filters from the to produce antimony oxide. The is an important source of uncertainty in production of antimony oxide. (E) smelting of a ore concentrate above the our analysis. K177 Slag from the production of fusion point is defined as mineral As indicated previously, for wastes antimony oxide that is disposed of or processing (See 54 FR 36618). At these managed on-site we based our speculatively accumulated (T). antimony oxide facilities, since mineral assessment of human exposures on the Other wastes generated by the processing has begun, wastes from the plausibility of ground water being used antimony oxide industry do not meet process are not eligible for the Bevill for drinking water. While some the criteria set out at 40 CFR exemption as beneficiation wastes (See information was available on utilization 261.11(a)(3) for listing a waste as 40 CFR 261.4(b)(7)(i)). In addition, of ground water for drinking water, very hazardous. They do not pose a although there is a Bevill exemption for limited information was available from substantial present or potential threat to 20 specific mineral processing wastes which to determine the location of human health or the environment. We form various mineral processing sectors, exposure at a given site. For wastes identified no risks of concern associated the wastes generated from antimony managed off-site we assumed that with the current management of these oxide mineral processing are not ground water is used for drinking water other wastes. included as one of these 20 wastes and (or will be in the future) and we used b. Description of the antimony oxide are not excluded. (See 40 CFR national data on the distribution of industry. Antimony oxide was produced 261.4(b)(7)(ii)). Thus there are no distances to residential wells to assess by four facilities in the United States in antimony oxide wastes that qualify for human exposures and risk. Our analysis 1998. Antimony oxide is used as a flame the Bevill exemption. did not consider possible changes in the retardant in plastics and textiles, a d. Wastes generated by these location of on-site waste management smoke suppressant, a stabilizer for processes. Table III–1 summarizes our operations in the future. These exposure plastics, an opacifier in glass, ceramics information about the wastes generated assumptions (about which there is and vitreous enamels, and a coating for from the production of antimony oxide:

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TABLE III±1.ÐANTIMONY OXIDE PRODUCTION WASTES

Number of Waste category reported 1998 volume Reported waste Management practices generators (MT) hazard codes

Antimony slag not recycled in process ...... 3 113 D008 ...... Sent to lead smelters for lead and/or anti- mony recovery; or on-site drum storage prior to future on-site land disposal. Baghouse filters ...... 4 9 No code reported ..... In-process antimony recovery; off-site anti- mony recovery; industrial Subtitle D landfill; or non-hazardous waste inciner- ator. Empty supersacks ...... 1 15 No code reported ..... Disposal in off-site Subtitle D landfill or re- cycled.

In addition to these wastes, there are site engineered ‘‘slag storage pit’’ to be unit for this waste, we assessed the on- other materials produced that are reused constructed in the next two to three site landfill scenario for this waste. in the antimony oxide production years. How Was This Waste Category process. Antimony oxide and antimony We assessed the on-site disposal Characterized? slag are captured at various points in the scenario, reflecting the projected facility and reinserted into a furnace to We selected two of the three facilities management practice for this waste. For produce antimony oxide, either on-site for sampling and analysis. At the site a number of years, the facility has been or off-site. Because these materials are which stores the slag indefinitely, we managed prior to reuse in ways that placing approximately 20 MT/yr in steel collected one sample of ‘‘reduction present low potential for release, and drums on pallets on the ground. The furnace slag’’ that was designated as because we evaluated process waste facility reported that they intend to containing less than 5 percent antimony generated after the secondary materials reclaim the antimony from this slag (AC–1–AO–01) and one sample of are reinserted into the process, we do when antimony prices are favorable. We ‘‘reduction furnace slag’’ that was not believe that these secondary consider storage on-site for more than designated as containing between 5 and materials present significant risks. one year to be speculative accumulation 10 percent antimony (AC–1–AO–06). e. Agency evaluation. (1) Antimony and consider these materials to be solid Based on characterization information slag not recycled in antimony oxide wastes. We believe that the length of provided by the facility in its RCRA process. time secondary materials are Section 3007 Survey response, we accumulated before being recycled is an believe these samples are representative How Are These Wastes Currently important indicator of whether or not of all of the slags generated at the Managed? they are wastes. This is supported by facility. We conducted total, TCLP and Three facilities produced antimony the large number of recycling damage SPLP analyses of these slags. The slag that is not recycled in the antimony cases where secondary materials that analytical results for the constituents oxide process. Two of these facilities were overaccumulated over time caused found to be present in the leachates at send the slag to lead smelters. One of extensive harm. (See 50 FR 614) ‘‘Under levels exceeding the HBLs are presented the two facilities reported its slag to be RCRA and the implementing in Table III–2. TC hazardous because of its lead regulations, permanent placement of We collected a third sample (LI–1– content (D008). The third facility, hazardous waste, including perpetual AO–01) at a facility that reclaims its slag however, has historically stored a for lead. This sample failed the TC for ‘‘storage’’ falls into the regulatory portion of its slag on-site in drums, lead, as the facility reported in its RCRA category of land disposal.’’ 25 (See also reporting that they plan to reclaim Section 3007 Survey response. The American Petroleum Institute v. EPA, antimony when antimony prices are results are available in ‘‘Waste more favorable. Recent revisions to the 216 F. 3d 50 (D.C. Cir. 2000).) Since the Characterization Report, Laurel facility’s Operating Permit,24 however, Operating Permit requires the facility to Industries Inc., La Porte, Texas’’ in the require that the slag be placed in an on- build and use an on-site, land-based docket for today’s proposal.

TABLE III±2.ÐCHARACTERIZATION OF SPECULATIVELY ACCUMULATED ANTIMONY SLAG

AC±1±AC±01 AC±1±AO±06 HBL Constituent of concern Total TCLP SPLP Total TCLP SPLP mg/L mg/kg mg/L mg/L mg/kg mg/L mg/L

Antimony ...... 11,500 55.8 114 127,000 110 211 0.006 Arsenic ...... 301 2.0 2.9 478 3.1 3.8 0.0007 Boron ...... <500 9.8 9.3 <2,500 8.5 8.1 1.4 Selenium ...... <50 0.6 0.6 <250 0.6 0.3 0.08 Vanadium ...... <50 1.3 1.1 <250 0.6 1.0 0.14

24 ‘‘United States Antimony Corp. Stibnite Hill the State of Montana on August 12, 1999 (with a Chairman, Subcommittee on Commerce, Mine Project Operating Permit 00045’’, 6th review number of stipulations), and subsequently approved Transportation, and Tourism, Committee on Energy draft, January 1999. This draft permit is issued by the Forest Service. and Commerce, House of Representatives, from J. under the Metal Mine Reclamation Act, 82–4–301 25 ‘‘Above Ground Land Emplacement Facilities, Winston Porter, Administrator, EPA, dated March MCA. It was prepared by the facility, approved by N.J. Law,’’ Letter to Honorable James J. Florio, 26, 1986.

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How Was the Groundwater Ingestion results are higher than the TCLP results, facility and any potential groundwater Risk Assessment Established? making the industrial landfill the worst plumes associated with its operation. case scenario. Specifically, we modeled potential We modeled the annual volume We examined records available from distances to wells from the facility’s reported to be stored on-site indefinitely the State where the slag is stored to southern boundary to one mile. (20 MT). (The facility reports that it determine the appropriate distance-to- processes sodium antimonate from two We used a regional site-based well to model. We identified four approach in modeling this unit, as facilities and returns the resultant slag residential wells within several miles of to the process for further processing. We described in section III.E.4. We the facility. These data demonstrate that modified this to enable us to use did not include these recycled slag groundwater is a viable and actively volumes in our modeling.) available depth to groundwater used resource in this area. One well is information at this particular site. We used the total and SPLP results as located 1.4 miles directly downgradient. model inputs, reflecting the industrial Based on local topography and What Is EPA’s Listing Rationale for This nature of the on-site unit. We used only groundwater information, we do not Waste? the analytical results for the facility that believe the other identified wells could stores the slag indefinitely. Both of the be affected by releases to groundwater Where these slags are reused and samples for this facility are relevant from the facility. We modeled potential present no exposure route of concern, because they represent the material releases to a downgradient residential we did not evaluate these secondary stored on-site and destined for the on- well. Given that our groundwater model materials further. site slag pit. We did not model the is not configured at this time to model The results of the risk assessment for sample from the other sampled facility releases further than one mile, we did the on-site disposal scenario for boron, because they acknowledged that their not assess the full distance to the known selenium, and vanadium were very low. waste exhibited the TC. Both this well. In our probabilistic analysis, we In the 90th to the 95th percentile range, facility and the facility that was not varied the well distance from the closest the highest hazard quotient for these sampled reclaim these wastes in a property boundary that appeared to be three constituents was in the range of manner that is excluded from regulation potentially downgradient to the limit of 0.001. For this reason, the full results for under Subtitle C. We believe that it is the model (one mile). Our results these three constituents are not reasonable to assume that they will therefore are conservative with respect presented here. The results of the risk continue to manage their slags in ways to this particular well, but otherwise assessment for the on-site disposal that do not violate Subtitle C reflect the fact that future residences scenario for antimony and arsenic are regulations. Also, in this case, the SPLP and wells may be placed closer to the presented in Table III–3:

TABLE III±3.ÐPROBABILISTIC RISK ASSESSMENT RESULTS FOR SPECULATIVELY ACCUMULATED ANTIMONY SLAG

Percentile Adult risk Child risk Adult risk Child risk

1Antimony hazard quotient 1ArsenicÐcancer risk

90th% ...... 2.2 4.6 4 E±07 3 E±07 95th% ...... 4.5 9.4 1 E±06 9 E±07

For a more complete description of this place the waste in an on-site lined More generally, we considered the analysis, see ‘‘Risk Assessment for the storage pit, upon completion of efficacy of landfills (and any liners) over Listing Determinations for Inorganic construction, that will be governed by a the modeled risk assessment period, Chemical Manufacturing Wastes’’ state mining permit. We considered which covers 10,000 years. Landfills are (August 2000) in the docket for today’s whether our decisionmaking should used actively until their capacity is proposal. account for the added protection reached (our models assume an active In our modeling results, the dilution provided by a liner system. Our first life of 30 years), and at the end of their and attenuation factors (DAFs) were consideration is the current uncertainty active life, we assume landfills are relatively high. For example, high end regarding this waste’s disposition. closed and the wastes remain in the unit antimony DAFs were as high as 8,000. While the facility has stated its intended indefinitely. The effectiveness of liner This is the result of the hydrogeological placement of this waste in a lined unit, systems depends on how they are setting of the site evaluated. Due to the our most recent information indicates designed. Composite and double liners high hydraulic conductivity we used in that construction had not yet begun. The that combine two or more layers of liner modeling, the landfill leachate is readily facility may in fact choose to place this material with leachate collection and diluted into a large volume of waste in an off-site commercial landfill leak detection will no doubt minimize groundwater. Given the uncertainty that would not necessarily be lined. leakage to the subsurface during the about the actual ultimate management This uncertainty is greater than in most period when the leachate collection practice and the site-specific nature of waste management scenarios that we system is actively managed. However, the modeling, DAFs could be have assessed in this rulemaking, where depending on the regulatory controls considerably lower in other disposal there is a long term history of relevant for a particular unit, monitoring scenarios, resulting in much higher management in a particular type of would continue for a limited post- hazard quotients and, therefore, higher management unit (e.g., an operating on- closure period. There is also uncertainty potential risks. site landfill, a local off-site landfill). associated with liner performance, in Our modeling approach assumes that Because of this uncertainty, we are the near term as well as in the long term. the slag will be placed in an unlined hesitant to give much weight to a liner There are a variety of factors that may unit. Information from the facility, system that may be constructed in the influence longevity and performance, however, indicates that they plan to future. such as poor construction, installation

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00021 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55704 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules or facility operation, or geologic proposal. However, we note that the its baghouse filters to Mexico for movement below the liner that can effectiveness of the liner system would antimony recovery. Two other facilities cause holes, tears or larger failures. have to be sufficient to reduce the dispose of these wastes in a non- Some defects may have a significant antimony concentration at the well by hazardous waste incinerator and an effect. Because of our uncertainty close to 90% in order to keep the risks industrial Subtitle D landfill. None of regarding the efficacy of the liner system below an HQ of 1. these wastes are handled as hazardous, over long periods of time, and the Therefore, given the reasons cited although our sampling efforts showed uncertainty over the ultimate disposal above, we propose to list these slags as this waste to exhibit the toxicity for this waste, we believe our use of the hazardous: characteristic for lead and arsenic. modeling results for an unlined landfill K177 Slag from the production of How Was This Waste Category is appropriate. antimony oxide that is disposed of or Characterized? In deciding whether to list this waste speculatively accumulated. as hazardous, we also considered other It is important to note that this listing We collected a total of three samples factors in addition to the risk results has been developed to capture only of this waste category from two noted above. First, we considered the those wastes that are not recycled. Thus, facilities. At one facility we collected very high levels of toxic constituents this listing, as proposed, would not one sample of the ‘‘oxidation furnace’’ present in the waste and in test leachate apply to generators that recycle or baghouse filters (AC–1–AO–03) and one (which is one of the criterion cited in reclaim this material as long as it is not sample of the ‘‘reduction furnace’’ 261.11(a)(3)(ii)). The levels of antimony speculatively accumulated. If slags have baghouse filters (AC–1–AO–07). At the and arsenic are quite high. The been speculatively accumulated (i.e., other facility, we collected a sample of antimony level exceeds 10% in the held for more than a calendar year the baghouse associated with its kiln waste (up to 127,000 mg/kg), and the without recycling) at the time of the (LI–1–AO–03). Because the facilities SPLP antimony concentration exceeds effective date of this final rule, these sampled represented the range of the drinking water HBL by a factor of slags would meet the listing production practices within the >35,000. Another key factor is the lack immediately.26 industry, we believe these samples are of any appreciable degradation expected We also propose to add antimony to representative of all of the baghouse for these metals (a constituent’s Appendix VII to Part 261, which filters generated by this industry. We degradation or persistence is also a designates the hazardous constituents conducted total, TCLP and SPLP criterion for listing given in for which K177 would be listed. analyses of these baghouse filters. The 261.11(a)(3)). Unlike some organic (2) Baghouse filters. analytical results for the constituents compounds, metals such as antimony found to be present in the leachates at will not degrade over time. Thus, even How Are These Wastes Currently levels exceeding the HBLs are presented if the loss in effectiveness of a liner Managed? in Table III–4. Two of the three samples system only occurs over the very long These filters capture product or off- of the waste, one from each facility that term, the metals would still be present specification product. Two facilities generate this waste, exceed the toxicity for leaching. It is difficult to assess the place antimony laden baghouse filters in characteristic for either lead or arsenic. impact of the long-term effectiveness of their on-site production furnaces. One (The third sample exhibits TCLP lead the liner system in question for today’s of these facilities also sends a portion of levels close to the TC standard). TABLE III±4.ÐCHARACTERIZATION OF BAGHOUSE FILTERS FROM ANTIMONY OXIDE PRODUCTION (MG/KG OR MG/L)

LI±1±AO±03 AC±1±AC±03 AC±1±AO±07 TC Constituent of Concern HBL Total TCLP SPLP Total TCLP SPLP Total TCLP SPLP Limit

Antimony ...... 91,400 9.3 6.2 150,000 9.9 4.3 145,000 68.7 287 0.006 ...... Arsenic ...... 114 <0.5 0.6 <250 <0.5 0.09 <250 1 6.9 6.9 0.0007 5.0 Boron ...... 24.0 6.5 1.0 <2500 <2 0.2 <2500 <2 0.7 1.4 ...... Cadmium ...... 5.3 0.3 0.5 <250 0.3 0.3 411 <0.05 0.9 0.0078 1.0 Lead ...... 3.1 1 8.5 16.9 <2500 2.8 1.0 <250 <0.5 <0.05 0.015 5.0 Mercury ...... 0.9 <0.002 0.001 0.1 <0.002 <0.0002 95.2 0.03 0.4 0.0047 0.2 Thallium ...... <2 <2 0.06 <1000 <2 0.06 <1000 <2 0.1 0.0013 ...... 1 Exceeds Toxicity Characteristic level.

What Is EPA’s Listing Rationale for This regulations. We propose to list this risk assessment modeling of the off-site Waste? waste under the 261.11(a)(1) criteria: landfill scenario, as we would traditionally do to support a 261.11(a)(3) We propose to list the baghouse filters K176 Baghouse filters from the production of antimony oxide (E). listing. Such modeling would reflect waste because our data show it reported management practices. routinely exhibits one or more of the Because we believe we have sufficient Antimony is not a TC constituent and, characteristics of hazardous waste (i.e., reason to list this waste under therefore, was not considered in the TC lead or arsenic), yet the generators 261.11(a)(1) based on the TC 261.11(a)(1) listing decision. However, do not identify their wastes as exceedences and lack of compliance exhibiting the toxicity characteristic and with hazardous waste regulation, we antimony levels are high and would the generators that dispose of this waste chose to conserve our time and likely result in risk if modeled. Leach do not comply with Subtitle C resources and did not conduct formal results for the waste exceed the HBLs by

26 A material is not accumulatively speculatively, the calendar year (commencing on January 1)—the material accumulated at the beginning of the however, if the person accumulating it can show amount of material that is recycled or transferred period. (40 CFR 261.1(c)(8)) that the material is potentially recyclable and has to a different site for recycling equals at least 75 a feasible means of being recycled and that—during percent by weight or volume of the amount of that

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00022 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules 55705 a wide margin, e.g., the SPLP results for pose hazardous at levels below the TC carbonate for commercial sale. A antimony are up to 48,000 times the (see 55 FR 11799, March 29, 1990). Pennsylvania facility produces barium HBL. The high levels of antimony in the Under an amended consent decree carbonate only for use as a feedstock in waste (up to 15%) would provide a (Environmental Technology Council v. its own internal manufacturing long-term source of the metal for Browner, C.A. No. 94–2119 (TFH), April processes. A third facility is a specialty leaching into the groundwater. Thus, we 11, 1997), EPA is required to sign a manufacturer that produces extremely expect that modeling an off-site Subtitle notice taking final action with respect to small amounts of barium carbonate D scenario would yield significant the proposed revisions to the mixture (approximately 10 kg in 1998).28 For drinking water risk. rule by April 30, 2001. more detailed information concerning Note that, when facilities process the (3) Empty supersacks. One facility this industry, see ‘‘Barium Carbonate antimony oxide product captured in ships crude antimony oxide in Listing Background Document for the these filters by reinserting the product- supersacks and then reuses them to Inorganic Chemical Listing containing filters back into the furnace store intermediate materials until they Determination’’ in the docket for today’s where the antimony oxide originated, wear out. The facility then sends these proposal. without reclamation, these materials empty supersacks either to an off-site Barium carbonate (BaCO3) has a wide 27 would not be solid wastes. industrial Subtitle D landfill or to an off- range of uses, including feedstock for We also propose to add arsenic and site plastic recycler. The facility claims production of other barium chemicals, lead to Appendix VII to Part 261, which that the supersacks are empty and an additive in various glasses, ceramics, designates the hazardous constituents would meet the standard in 40 CFR bricks, and other construction materials, for which K176 would be listed. 261.7 (which exempts ‘‘empty’’ an additive in oil-drilling suspensions, The ‘‘mixture’’ rule for listed wastes containers formerly used to manage and a brine purification chemical in the currently provides an exemption for hazardous waste). Although 40 CFR chlor-alkali industry. wastes listed solely because they exhibit 261.7 does not literally apply to these The two primary barium carbonate characteristics (see 40 CFR sacks, we think it is reasonable to take production facilities use different 261.3(a)(2)(iii)). Mixtures of such listed a similar approach here. We believe that manufacturing processes to make wastes lose their listed waste status the levels of crude antimony oxide in barium carbonate. The Georgia facility when they cease to exhibit worn-out supersacks would be low uses locally mined barite ore, containing characteristics for which they were because the material is the primary barium in the form of barium sulfate, as listed. (However, they would still need feedstock (raw material) used in this the primary feedstock. The ore is to comply with Land Disposal process. We do not believe it follows crushed and milled, thermally reduced Restriction requirements.) In the both of that these supersacks should be in a roasting kiln, and leached with the last two Hazardous Waste regulated, when other similarly empty water to dissolve the barium. The Identification Rule (HWIR) proposals containers would be exempt. Therefore, resulting barium sulfide solution is (60 FR 66344, December 21, 1995) and we propose not to list this waste as filtered and reacted with carbon dioxide (64 FR 63382, November 19, 1999), we hazardous. gas to produce a barium carbonate proposed to narrow the exemption to precipitate. This precipitate is then only include wastes listed for 2. Barium Carbonate dried, and sized for sale. ignitability, corrosivity, and reactivity. a. Summary. We have evaluated the The Pennsylvania facility uses a This narrowing would make any wastes, waste management practices, commercially purchased high purity waste listed for the toxicity and potential risk exposure pathways barium chloride solid as the primary characteristic (TC) (including the waste associated with the barium carbonate feedstock. The facility dissolves the proposed today for listing under the production processes and propose not to barium chloride in water, heats and (a)(1) criteria) ineligible for the current list any wastes from this industry as filters the resulting solution, and exemption. In other words, under hazardous under Subtitle C of RCRA. precipitates barium carbonate by current mixture rule regulations, Some wastes in this industry are D002 reacting the barium chloride solution mixtures containing these baghouse or D005 characteristic hazardous wastes, with ammonium bicarbonate. The filters would become nonhazardous which are both currently subject to resulting barium carbonate precipitate is wastes once they ceased exhibiting the RCRA Subtitle C regulation and washed, filtered, dried and sized before characteristic. Under the HWIR managed in compliance with those the facility utilizes it as a feedstock in proposal, however, such mixtures regulations. For other wastes, not other manufacturing processes on-site. would remain hazardous wastes even identified as characteristic hazardous after they cease to exhibit the TC. As we wastes, we have identified no risks of c. What wastes are generated? Table state in the TC rule, chemicals can still concern associated with the current III–5 below briefly lists the facility- management of these wastes that would reported residuals from the barium 27 As noted above, these filters capture product warrant listing. These wastes do not carbonate manufacturing processes, materials. EPA does not regulate reclamation of meet the criteria listed under 40 CFR residual volumes generated in 1998, these products. See 50 FR 14216, April 11, 1985: 261.11(a)(3) for listing a waste as reported RCRA hazard codes, and ‘‘Under the final rules, commercial chemical residual management practices. products and intermediates, off-specification hazardous. variants, spill residues, and container residues b. How is barium carbonate listed in 40 CFR 261.33 are not considered solid produced? There are two facilities in the 28 Since, as explained below, we find no wastes when recycled except when they are significant risks from the larger volume wastes we recycled in ways that differ from their normal use— United States that produce significant assessed, we conclude that any low volume wastes namely, when they are burned for energy recovery quantities of barium carbonate. A from this third facility also would not pose any or used to produce a fuel’’ Georgia facility produces barium risks warranting listing.

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TABLE III±5.ÐBARIUM CARBONATE PRODUCTION WASTES

Reported RCRA Waste category 1998 volume (MT) hazard codes Sequential residual management practices

Barite Ore Feedstock ProcessÐGeorgia Facility

Treated barium wastes (D005 barium wastes in- 18,300 ...... None (D005 prior Disposal in local, captive, industrial Subtitle D clude barite ore leaching waste, barium sulfide to treatment). landfill (after treatment of D005 wastes in on- filtration sludge, and barium carbonate produc- site Subtitle C treatment unit). tion area cleaning and maintenance wastes). Wastewater from BaCO3 precipitate dewatering .. 313,000 ...... None ...... Treatment in on-site, tank-based WWTP prior to NPDES discharge to Etowah River. WWTP sludge ...... 11,000 ...... None ...... (1) Dewatered; (2) Treated on-site; (3) Disposal in local, captive, industrial Subtitle D landfill. Spent polypropylene and nylon filter media and 3 (filter media) ...... None ...... (1) Washed and washwaters re-inserted to bar- baghouse dust collector bags. ∼1.5 (baghouse ium carbonate production process. Solids bags). managed as barium carbonate production area cleaning and maintenance wastes. (2) Treated materials disposed in off-site munic- ipal Subtitle D landfill.

High Purity Barium Chloride Feedstock ProcessÐPennsylvania Facility

Ammonia vapor scrubber water and ammonia Not reported ...... D002 ...... Treatment in on-site, tank-based WWTP. reclamation unit wastewaters. Barium carbonate precipitate washwater ...... 1,600 ...... None ...... Treatment in on-site, tank-based WWTP prior to NPDES discharge to Susquehanna River. WWTP sludge ...... 8,200 ...... None ...... (1) Stored in roll-off bin; (2) Disposal in off-site municipal Subtitle D land- fill. Ammoniated spent process solution storage tank 1 ...... None ...... Disposal in off-site municipal Subtitle D landfill. solids. Sludge and spent filter media from filtration of <1.23 ...... D005 ...... (1) Stored in closed container; barium chloride solution and BaCO3 drying and (2) Sent to off-site Subtitle C facility for treatment sizing unit dusts. and disposal.

In addition to these wastes, the two material is a gas from a production unit, production of ammonium bicarbonate barium carbonate manufacturing rather than from a waste management solution for use in the barium carbonate facilities also produce other materials unit, and is conveyed to its destination production process. Because the spent which are either piped directly back to through piping, the gas is not a solid solution is piped to the reclamation unit the production process or are used for waste. RCRA Section 1004(27) excludes with no significant potential for other purposes. Residues from the barite non-contained gases from the definition exposure to the environment, we did ore feedstock production process, ore of solid waste, and therefore they cannot not evaluate the solution further. crusher/grinder, kiln, barium carbonate be considered a hazardous waste (see 54 Both facilities produce barium drier, granulation and packaging FR 50973). carbonate from a saleable mineral processes are directly returned to their The facility using barium chloride as product.29 Under the Bevill exemption unit of origin with no significant its feedstock reclaims ammonia in the (54 FR 36620–21), chemical pathways for exposure of these form of ammonium hydroxide from manufacturing begins if there is any materials to the environment prior to barium carbonate production wastes further processing of a saleable mineral reuse. Barium carbonate production area and uses this material throughout the product. Since these facilities use cleaning and maintenance wastewaters facility as a feedstock and reagent. Spent saleable mineral products as feedstock, are also re-inserted to the barium ammoniated process solution is piped their processes are chemical carbonate production process with no from the process unit where it forms to manufacturing, and are not classified as significant pathways for exposure of a storage tank where it is commingled mineral processing. Therefore none of these materials to the environment prior with ammoniated spent process the wastestreams generated by these to reuse. Because these materials are solutions from several other on-site facilities during the production of managed prior to reuse in ways that manufacturing processes. The barium carbonate are Bevill exempt. present low potential for release, and ammoniated spent process solutions See the ‘‘Barium Carbonate Listing because we evaluated all wastes from these other manufacturing Background Document for the Inorganic generated after they are reinserted into processes are beyond the scope of this Chemical Listing Determination’’ for the process, we do not believe that these listing determination. From the storage more details on these residuals. secondary materials present significant tank, the facility pipes the commingled threats. ammoniated spent process solutions to 29 Note that primary barite ore has wide use in The barite ore feedstock facility also an ammonia reclamation unit which drilling muds for the petroleum industry and produces molten sulfur or sodium reclaims the ammonia in the form of numerous other industrial uses, including use as feedstock for barium chemicals; see ‘‘Barite’’ U.S. hyposulfate from hydrogen sulfide gas ammonium hydroxide. Ammonium Geological Survey—Minerals Information, 1997, piped from the barium carbonate hydroxide is used on-site in various http://minerals.usgs.gov/minerals/pubs/ manufacturing process. Because the manufacturing processes, including the commodity/barite/index.htm.

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d. Waste characterization and Agency characteristically hazardous for barium that exceeded the health-based levels by evaluation. Barium is the primary (D005) before treatment (or are more than a factor of 2 (see section constituent of potential concern in the consistently assumed by the facility to III.E.3 for a discussion of this risk- wastes from both facilities. Barium be D005 wastes), include: screening criterion). See the ‘‘Barium occurs in several production wastes at —Barite ore leaching waste, which is Carbonate Listing Background high levels, in some cases exceeding the solids from the filtration of the liquid Document for the Inorganic Chemical TC level (100 mg/L) in TCLP leachate product stream from the barite ore Listing Determination’’ for further samples. These TC wastes are coded and roasting and leaching units, details on the available data. treated as hazardous (D005). The —Barium sulfide sludge, which is from In addition, we found only one Georgia facility holds a hazardous waste polishing filtration of liquid barium exceedence of AWQC standards among treatment permit to allow on-site sulfide, and, the SPLP leaching data for treated stabilization of barium, and the —Wastes from cleaning and barium wastes. Selenium was found at Pennsylvania facility sends all of their maintenance of the barium carbonate a level of 0.04–0.06 mg/L, which D005 wastes off-site for treatment and production area. exceeds the AWQC standard (0.0050 mg/L) by a factor of 8 to 12. However, disposal at a hazardous A RCRA Subtitle C hazardous waste the landfill in which the treated barium and disposal facility. treatment facility permit governs the on- We decided not to do characterization wastes are placed is 1,700 feet from the site treatment process for these barium sampling for wastes from either facility nearest downgradient water body, the wastes. The three wastes are sent because both facilities submitted Etowah River, and also lies beyond the directly to the treatment unit, or they information to us on the nature of their river’s 100 year flood plain. In recent are stored prior to treatment for short wastes. We also received some years, the Etowah River in the vicinity additional analytical data from the State time periods in Subtitle C closed of the landfill has had a flow rate of Georgia for the Georgia facility. These containers. The treatment process is a varying between 9.9 to 230 m 3 per data provided information on the stabilization process for barium using second on a daily basis. Given the concentrations (or absence) of the metal gypsum (primarily calcium sulfate) to distance over which leachate from the constituents of potential concern in the precipitate soluble barium as less treated barium wastes would need to wastes and in test leachates from the soluble barium sulfate. According to travel before reaching the river, dilution wastes. We believe the available RCRA Subtitle C regulations, the treated and attenuation during transport in information is sufficient to adequately barium waste must meet the LDR UTS. local groundwater, and further dilution characterize the wastes and to allow us Treatment takes place in concrete in the Etowah River, we believe the to evaluate their risk potential for the mixer-type trucks. Once treatment is levels of selenium in the leachate would purposes of a listing decision. ‘‘Barium complete, the treatment trucks decrease to a level which would no Carbonate Listing Background immediately transport the waste to the longer pose a risk to the environment. Document for the Inorganic Chemical facility’s captive Subtitle D landfill for We do not believe it is necessary to Listing Determination’’ summarizes the disposal, located approximately 2 miles assess other management practices for analytical data and other information from the production facility on facility- the treated barium wastes. The facility available for these wastes. owned property. has treated and disposed of their We propose not to list any of the State and facility information indicate treatment residues in a similar manner wastes from the barium carbonate that the treated barium wastes no longer for over 15 years. The production manufacturing industry. Many wastes exceed the TC level for barium (100 mg/ facility itself relies on a local source of from this industry are characteristically L from TCLP analysis) and typically barite ore, has operated from its current hazardous and managed as hazardous leach less than 1 mg/L barium, location since 1942 and is therefore not wastes either on-site or at permitted according to both SPLP and TCLP likely to change its location in the near Subtitle C treatment facilities off-site. analyses. In addition, according to data future. The dedicated landfill has a Other wastes did not exhibit the facility and the state of Georgia remaining life of nearly 20 years and is constituents at levels of concern for submitted to EPA from sampling events located approximately 2 miles from the purposes of a listing given the nature of conducted during the past two years at production facility. Given the dedicated their management and disposal. the facility, the waste meets the LDR nature of the landfill, its proximity to Several groups of wastes from each of UTS for all regulated constituents. the production facility, and the the facilities are disposed of in a treated The treated barium wastes are significant remaining capacity, we form, rather than an as-generated form. disposed of in the landfill without daily believe it is unlikely that the Georgia In general, therefore, we focused our cover. However, the waste has a facility will dispose of their wastes in evaluation on the treated form of the relatively high moisture content any other unit in the near future. Thus wastes. (approximately 50%) when placed in there is no need to assess additional The paragraphs below describe how the landfill and, according to the management scenarios for this the wastes are generated and managed facility, hardens over time and does not wastestream. for the two processes and our rationale create dust. In addition, the waste does Given the facility’s Subtitle C waste for proposing not to list the wastes. We not contain any known volatile treatment permit, we believe that the solicit comments on the proposed constituents of concern. facility’s untreated D005 wastes are listing decisions described below. To assess the potential for adequately managed with respect to this (1) Wastes from the production of groundwater releases from the captive, rulemaking. In addition, we have found barium carbonate from barite ore industrial landfill, we compared the no potential for releases to air, feedstock. (a) Treated barium wastes. SPLP leaching data from the facility and groundwater, or surface water at levels The waste category, ‘‘treated barium the state of Georgia to existing HBLs for of concern from the treated wastes. wastes,’’ is the treatment residue from ingestion of groundwater. SPLP data are Therefore we propose not to list these the commingling and treatment of appropriate for evaluating this waste wastes. several barium wastes in an on-site because it is placed in a Subtitle D (b) Wastewater from barium carbonate hazardous waste treatment unit. The industrial landfill. We did not find any precipitate dewatering. The facility barium wastes, which are consistently constituents in the available SPLP data filters barium carbonate precipitate from

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00025 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55708 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules residual process solutions and sends of airborne dust. In addition, the waste Given the relatively small volume of this filtrate to the facility’s tank-based does not contain any known volatile these wastes, the inert nature of the wastewater treatment plant (WWTP) for constituents of concern. filters and bags themselves, and the treatment. According to the facility’s We do not believe it is necessary to facility’s washing and stabilization of RCRA Section 3007 Survey response, assess other management practices for barium prior to disposal, we believe the wastewater does not exceed the TC this waste. The facility has treated and these treated bag wastes do not warrant level for any constituent. disposed of their wastewater treatment listing as hazardous wastes. Wastewater from the barium plant sludge in a similar manner for (2) Wastes from the production of carbonate production process over 15 years. Given the dedicated barium carbonate from high purity commingle in the WWTP with nature of the landfill, its proximity to barium chloride feedstock. (a) Barium wastewaters from other facility the production facility, and the carbonate production wastewaters and processes beyond the scope of this significant remaining capacity, we wastewater treatment plant sludge. The rulemaking and comprise approximately believe it is unlikely that the facility Pennsylvania facility commingles and 17% of the total WWTP flow-through. will dispose of their wastes in any other treats wastewaters from several The wastewater treatment is an facility in the foreseeable future. manufacturing processes at their facility oxidation process. Treatment of the Based on our knowledge of the in an on-site, tank-based WWTP. wastewaters occurs in tanks equipped current nature of the management of the Wastewaters from the barium carbonate with secondary containment. Given the treated wastewater treatment plant production process are piped directly to controlled manner in which the sludge and of the low level of the WWTP and comprise less than 1% wastewater is managed in tanks, the constituents of concern it contains, of total WWTP flow through; the lack of any volatile constituents of including volatile constituents, we remainder of the wastewaters entering concern, and NPDES regulation of the propose not to list the treated the WWTP are from manufacturing WWTP effluent, we propose not to list wastewater treatment plant sludge. processes not within the scope of this this wastewater. (d) Spent polypropylene and nylon listing determination. Wastewaters from (c) Treated wastewater treatment filter media and baghouse dust collector the barium carbonate production plant sludge. The facility’s WWTP bags. Baghouse dust collector bags and process include: generates a treatment sludge from the polypropylene and nylon filter media —Ammonia vapor scrubber waters and commingling and treatment of fabric at the Georgia facility deteriorate wastewaters discussed above in the over time and must be replaced ammonia reclamation unit preceding section. The resulting sludge periodically. The facility washes the wastewater. —Barium carbonate precipitate is dewatered to 25% solids content in bags and filters with water and then an uncovered tank. None of the soaks them in sulfate solution to washwater. information the facility provided on this stabilize any remaining barium. The A scrubber captures ammonia vapor waste indicates the presence of volatile facility then disposes of the bags and from the mixing of ammonium constituents of concern. filter fabric in a local municipal Subtitle bicarbonate solution with the barium The facility places the dewatered D landfill. Wastewaters from the chloride solution to precipitate barium WWTP sludge directly from the WWTP washing of the filters and bags are carbonate. Water, sodium hydroxide, unit into a treatment unit consisting of returned to the production process. and emissions from other manufacturing a concrete mixer-type truck containing Solids from the washing of the filters processes in the facility mix with the gypsum (primarily calcium sulfate). The and bags become part of the cleaning ammonia vapor in the scrubber to truck mixes the wastewater treatment and maintenance wastes that are treated produce this wastestream. sludge with the gypsum to convert as discussed above in section (a). An ammonia reclamation unit soluble barium to a less soluble barium The facility did not provide chemical recovers ammonia from ammoniated sulfate prior to transporting the waste to composition analyses for these wastes. spent process solutions from multiple the facility’s off-site, captive, Subtitle D However, we do not expect either manufacturing processes, including the landfill. We found low potential for baghouse bags or nylon and barium carbonate manufacturing releases from either the dewatering tank polypropylene filter fabrics, which are process, in the form of 28% ammonium or the treatment unit. Analytical data used primarily for physical separation hydroxide solution. The unit also from the state shows that the treatment of solids from liquids in the barium produces a wastewater. Approximately process reduced leachable barium in the carbonate production process, to 1% of the total ammonia reclamation sludge, according to SPLP analysis, from contain notable levels of any potential unit inflow derives from the barium 53 mg/L to 0.03 mg/L. constituent of concern besides barium. carbonate production process. SPLP analytical data from the State According to the facility, neither the Therefore, a small percentage of the also show no potential constituents of bags nor the filters exceed the TC level unit’s wastewater derives from barium concern in treated WWTP sludge for any constituent. In addition, the carbonate production. samples at concentrations above HBLs facility treats the materials to stabilize The facility also produces a or above AWQCs. Therefore, this waste any remaining barium before disposing wastewater from the washing of barium screened out from any further risk of them in a Subtitle D municipal solid carbonate precipitate with deionized evaluation for groundwater or surface waste landfill. The facility does not water in order to remove any process water. The SPLP data are appropriate for produce a large volume of these wastes; solution remaining on the precipitate. evaluating this waste because it is approximately 3 metric tons per year of The only possible release route of placed in a Subtitle D industrial landfill. filters and approximately 1.5 metric concern from the tank-based system for Similar to the treated barium wastes tons per year of baghouse bags. Because the wastewaters would be through air described above in section (a), the waste barium is not volatile, and because we releases. This pathway is highly has a high moisture content when do not expect the filter media and bags unlikely for the nonvolatile metals that placed in the landfill and is reported by to contain any other volatile are the potential constituents of concern the facility to harden over time. constituents, we do not believe these in these wastes. Given the controlled Therefore, we do not believe this waste residuals pose any risk through airborne manner in which the wastewaters are poses a significant risk through releases pathways. managed and the regulation of the

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00026 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules 55709 treatment unit’s discharge under the The ammoniated spent process We have identified no risks of concern NPDES program, we propose not to list solution storage tank accumulates solids associated with the current management these wastewaters. which the facility removes and disposes of the wastes. Treatment of the commingled of in a local Subtitle D municipal solid b. Description of the boric acid wastewaters consists of neutralization waste landfill on a yearly basis. The industry. Boric acid was produced by followed by filtration. The treatment tank solids are a small volume waste of two facilities in the United States in generates a sludge. According to the 1 MT/yr. According to analytical data 1998. These two facilities are both facility’s RCRA Section 3007 Survey provided by the facility, the solids do located in the Mojave Desert in response, the sludge does not exceed the not exceed the TC level for any California, one of the few areas where TC level for any constituent. The facility constituent, though they do contain borate minerals can be mined in the disposes of the sludge in a local Subtitle vanadium, nickel, and antimony at United States. D municipal solid waste landfill. We do levels of potential concern. However, as The two facilities mine borates from note the presence of some potential noted for the wastewater treatment plant different sources to produce boric acid. constituents of concern in the WWTP sludge, the constituents of concern in The first recovers borate from brines sludge. These constituents include the solids are unlikely to arise from the pumped from beneath Searles Dry Lake, vanadium, nickel, and antimony. barium carbonate production process California. The second facility mines However, we do not believe that these because the barium carbonate sodium borate ores near Boron, constituents derive from the barium production process contributes only 1% California. carbonate manufacturing process. of the total wastewaters in the storage The first facility extracts highly Because the barium carbonate tanks. In addition, information the mineralized brine and uses a liquid- production process wastewaters facility provided indicates that the liquid extraction process to remove the contribute less than 1% of the total nickel, vanadium and antimony found borates from the brine. During the first input to the on-site WWTP, any in the sludge derive from other production step, called the ‘‘loading constituents in the barium carbonate manufacturing processes that are section,’’ the facility mixes the brine production wastewaters sent to the beyond the scope of this listing with a chelating agent in a kerosene WWTP also make a minimal determination. Thus, given the solids’ solution that causes most of the boron contribution to the total level of small volume and the low likelihood and some of the sodium and potassium constituents in the combined that the barium carbonate process compounds in the brine to bind to the wastewater in the WWTP and the wastewater contributes any constituents extractant. The loaded extractant is sent resulting sludge. In addition, the of concern, we propose not to list the through strippers where it is mixed with process uses high purity barium ammoniated spent process solution tank dilute sulfuric acid to strip the boron, solids in this listing determination. chloride dissolved in deionized water as sodium and potassium from the (c) Sludge and spent filter media from its primary feedstock and reclaims extractant to form boric acid, sodium filtration of barium chloride solution sulfate and potassium sulfate. The much of the residual ammonia from its and barium carbonate drying and sizing solution is then sent to a solution settler ammonium bicarbonate feedstock. unit air pollution control residues. Both from which the liquor goes to boric acid Therefore, the likelihood that the the air pollution control dusts from the recovery using crystallization and constituents of concern in the sludge barium carbonate drying and sizing unit evaporation techniques. might arise from the barium carbonate and sludge and the spent filter materials production process is very low. from barium chloride solution filtration The second facility mines sodium Moreover, the facility has provided exceed the TC regulatory level for borate kernite ore to produce boric acid information to us indicating that the barium (100 mg/L). The facility codes through a process of dissolution, barium carbonate process is not the the waste as characteristic hazardous classification, thickening, filtration and source of these potential constituents of waste (D005). The facility stores these crystallization. concern and that they derive instead small volume wastes in closed Because the facilities use such from on-site manufacturing processes containers on-site before sending them different sources and production beyond the scope of today’s listing to a RCRA Subtitle C hazardous waste processes, their resulting wastes are proposal (see ‘‘Barium Carbonate Listing treatment and disposal facility for very different and are discussed Background Document for the Inorganic treatment and disposal. We believe that separately. For more detailed Chemical Listing Determination’’ for the containers present no significant information concerning this industry, further details). Given the minimal potential for release to the environment. see the ‘‘Boric Acid Background potential for contribution of We believe that regulations applying to Document for the Inorganic Chemical constituents of concern by the barium characteristic wastes adequately protect Listing Determination’’ in the docket for carbonate process wastewaters to the against mismanagement. Furthermore, today’s proposal. WWTP sludge, we propose not to list these wastes comprise a very small c. Agency evaluation of wastes this sludge under this rulemaking effort. volume (<1.23 metric tons per year). generated by the brine recovery process. (b) Ammoniated spent process Thus, we propose not to list these Are There Any Wastes in This Process solution storage tank solids. The facility wastes. That Fall Under the Bevill Exemption? pipes residual process solution containing ammonia directly from the 3. Boric Acid The depleted brine from the loading barium carbonate precipitate settling a. Summary. We have evaluated the section of the brine recovery process is unit to covered storage tanks prior to wastes from the production of boric acid exempt as a mineral processing routing it through an on-site ammonia and propose not to list any wastes from beneficiation waste under 40 CFR reclamation unit. The barium carbonate this process as hazardous under RCRA. 261.4(b)(7)(i).30 This waste from the process wastewater is one of many These wastes do not meet the criteria set ammoniated residual process solutions out at 40 CFR 261.11(a)(3) for listing 30 The Agency has previously evaluated the Bevill status of wastestreams at the Searles Lake facility; the facility routes to the storage tanks wastes as hazardous. They do not pose see memos dated February 14, 1992 and June 30, and constitutes approximately 1% of the a substantial present or potential threat 1993 in Appendix E of the ‘‘Boric Acid Background unit’s total input. to human health or the environment. Continued

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00027 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55710 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules extraction/beneficiation of ores and an API settler and Wemco floatation —Petroleum contaminated sludges from minerals is thus outside the scope of the cells designed to separate organic containment areas around the API consent decree. The facility reported compounds from the brine. The organic settler, Wemco floatation cells, generating 4,600,000 MT in 1998. This emulsions generated in these units and loading section and liquid-liquid Bevill exempt waste is commingled in the process settlers are sent to an on- extraction (LLX) strippers with wastes which do not qualify for the site ‘‘crud’’ treatment facility which —Spent activated carbon collected from Bevill exclusion later in the process. breaks down the emulsion into aqueous the carbon filter system used to purify The portion of the waste which does not and organic components. This treatment the borate liquor before it goes into qualify for the Bevill exclusion is within process generates a non-exempt the crystallization units the scope of the consent decree and is hydrocarbon waste (fuel oil) that is sent discussed below. off-site to a used oil refinery. The Bevill In addition to the above wastes, the As discussed in the Agency’s prior exempt brine is sent to the ‘‘Trona facility also produces other materials Bevill evaluations for this facility, skimmer’’ where it is combined with during the production of boric acid that mineral processing begins at the liquid- other non-exempt wastewaters are either piped directly back to the liquid extraction step where sulfuric generated during the process. The Trona production process or used for other acid is added to the loaded extractant to skimmer acts as a settling pond purposes. These materials include produce sodium sulfate and boric acid. promoting phase separation of aqueous residuals and kerosene Wastes generated before this step, remaining organic materials in the recovered from the crud treatment including spent brine, are beneficiation brine. The Bevill exempt brine is then process, off-specification product, wastes and retain their Bevill returned to the dry lake for recharging scrubber water and condensate that are exemption. All wastes generated after as required by the facility’s Bureau of returned to on-site production units for the beginning of mineral processing are Land Management permit. Because the use. Because these materials are reused non-exempt solid wastes. Therefore, all non-exempt wastewaters are on-site in production units and there is of the wastes at this facility which are commingled with the Bevill exempt no significant potential for exposure of generated from the liquid extraction brine in the Trona skimmer, the non- these materials to the environment prior step to the end of the process are all exempt wastewaters are also returned to to reuse, we found that they present no non’exempt solid wastes. See the ‘‘Boric the dry lake as a small percentage of the significant threat. Also, off-specification Acid Background Document for the overall volume. The non-exempt organic product, when reinserted without Inorganic Chemical Listing waste removed at the Trona skimmer is reclamation into the process where it Determination’’ in the docket for more stored on-site in a tank until it is originated, is not a solid waste. information on the Bevill exemption for shipped off-site to a commercial blender wastes at this facility. and subsequently burned for energy How Are the Wastes From the Brine What Kinds of Wastes Are Generated by recovery. Recovery Process Currently Managed? the Brine Recovery Process? Additional wastes generated by the Table III–6 summarizes our The Bevill exempt depleted brine brine recovery process that are not information about the wastes from this from the loading section is sent through Bevill exempt include: process:

TABLE III.±6.ÐBORIC ACID: BRINE RECOVERY PROCESS WASTES

Waste category 1998 volume (MT) Sequential management practices

Fuel oil from crud treatment facility ...... 690 ...... (1) Stored in covered tank; (2) Sent off-site to a Subtitle C permitted used oil refinery. Miscellaneous wastewaters ...... 194,040 (The Bevill exempt partially depleted (1) Combined wastewaters; discharged to brine volume is 4.6 million MT). Trona skimmer with the Bevill exempt par- tially depleted brine; (2) Removal of organics in skimmer unit; (3) Commingled partially depleted brine and process wastewaters are returned to Searles Dry Lake for recharging. Organics from Trona skimmer ...... 10 ...... (1) Stored in covered tank; (2) Sent to off-site Subtitle C blender; (3) Burned for energy recovery. Sludges from containment areas ...... 20 ...... (1) Drum storage; (2) 20 cubic yard roll-off bins; (3) Transported with manifest off-site to Sub- title C landfill as California-only hazardous waste. Spent activated carbon ...... 43 ...... (1) Washed; (2) Reclaimed in an on-site furnace; (3) Reused in the process.

Document for the Inorganic Chemical Listing Determination’’ in the docket.

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What Is EPA’s Decision About Whether hydrocarbons). This wastewater is section, LLX strippers, Wemco flotation to List These Wastes as Hazardous? generated at the carbon column. cells and API settlers. The facility We propose not to list any wastes However, it only represents 0.03 percent reported a California-only hazardous from the brine recovery process for the of the total volume that is returned to waste code CA611 (petroleum production of boric acid. Our rationale the dry lake. Also, the reported level of contaminated soils) for the waste but for each waste is presented below. formaldehyde in the waste would be did not report any federal characteristic (1) Fuel oil from the crud treatment well below the HBL for this chemical (3 codes. The facility stores the waste on- 31 facility. We propose not to list the fuel mg/L) after mixing with other site in drums, transfers to it to 20 cubic oil generated at the crud treatment wastewaters. We are not concerned with yard roll-off bins and mixes the sludge facility. The facility characterized the potential air releases because the Trona with soil, and then ships the waste off- fuel oil as 100 percent hydrocarbons. skimmer, where the wastes are mixed, is site with a manifest as a California-only The fuel oil is stored on-site in a covered. The facility also mixes a hazardous waste to a Subtitle C landfill. covered tank prior to being shipped off- characteristic (D002) HCl acid waste The facility is tied to its location in site to a Subtitle C permitted used oil stream with the Bevill exempt depleted California so we believe it is plausible refinery. For those scenarios where brine prior to reaching the Trona that the waste will always be treated as a California-only hazardous waste. We wastes are managed in a tank, the skimmer. The resultant mixture is not characteristic and the mixing takes do not believe there would be any impervious nature of the construction place within a pipeline where there is significant benefit to the environment materials (concrete, fiberglass, or steel) no opportunity for exposure to the by listing this waste. of tanks is unlikely to result in releases characteristic waste before or during the (5) Spent activated carbon. We to groundwater in all but the most mixing. Given the factors listed above, propose not to list the carbon that is catastrophic scenarios. We also are not particularly the lack of an exposure regenerated on-site. The carbon is concerned with potential air releases pathway, we propose not to list the regenerated in an on-site furnace. The because the tank is covered. The miscellaneous wastewaters. carbon filtration process occurs later in subsequent treatment at the permitted (3) Organics from the Trona skimmer. the process after much of the organic used oil refinery is already regulated We propose not to list the organics additives have settled out of the borate under Subtitle C and the used oil (chlorinated hydrocarbons) recovered liquor. Consequently, we expect that the regulations. Therefore, we propose not from the Trona skimmer. The organics filters will not collect high to list this waste. are stored in a covered tank before being concentrations of constituents of (2) Miscellaneous wastewaters. We shipped off-site. For those scenarios concern, except perhaps kerosene propose not to list the miscellaneous where wastes are managed in a tank, the related organics. We expect any such wastewaters. We evaluated the potential impervious nature of the construction constituents that are filtered out using for an exposure pathway via materials (concrete, fiberglass, or steel) carbon adsorption to be combustible. groundwater ingestion and determined of tanks is unlikely to result in releases There is no potential for exposure prior that no such pathway exists. The facility to groundwater in all but the most to the regeneration process or during the producing boric acid by recovering catastrophic scenarios. We also are not return of the activated carbon to the borates mined from Searles Dry Lake is concerned with potential air releases carbon filter. The furnace is permitted located in California’s Mojave Desert. because both the Trona skimmer and by the State of California Air Control The process and associated wastewaters tank are covered. The waste is shipped Board. Although the permit does not are tied to the Mojave Desert location off-site to a Subtitle C permitted blender contain any requirements for emission because it is the source of the borate prior to being burned for energy controls, it does require annual rich brine. The environment is arid with recovery in cement kilns. Burning by reporting. We reviewed the emissions only 4 inches of precipitation annually. cement kilns is regulated under MACT data and do not believe that the The groundwater under the facility has standards for cement kilns (64 FR emissions from the furnace are of total dissolved solids (TDS) levels as 31989, June 14, 1999 and 64 FR 52827, concern. The reported emission levels high as 450,000 ppm. All wastewaters, September 30, 1999). Therefore, we did are significantly below the MACT including the Bevill exempt depleted not further evaluate potential risks from standards for permitted hazardous waste brine, are co-managed and ultimately burning the organics under this listing. incinerators (64 FR 52827, September returned to the dry lake resource. Due The facility reported a California-only 30, 1999). We expect the use of this to the extremely high TDS levels in the hazardous waste code CA343 (organic furnace to continue because it is area, the water is non-potable. The liquids, unspecified) for the waste but expedient to regenerate the carbon on- surrounding communities have drinking did not report any federal characteristic site, and the facility is unlikely to water piped in from 25 miles away. codes. The facility manifests the waste relocate given the proximity of the Therefore, no groundwater exposure using the California code when they mineralized brine source. Therefore, we pathway exists. send it to the blender. Because this propose not to list this waste. Furthermore, the total volume of the waste has significant BTU value and d. Agency evaluation of wastes miscellaneous wastewaters is 4 percent also carries a state hazardous waste generated by the kernite ore process. of the volume of the depleted brine; any code, we expect this management contaminants in these wastewaters What Kinds of Wastes Are Generated by practice to continue; we do not believe would therefore be diluted by a factor of the Kernite ore Process? there would be any significant benefit to 25 prior to return to the dry lakebed. The facility generates two primary the environment by listing this waste. Most of the miscellaneous wastewaters wastestreams: and gangue. The (4) Sludges from containment areas. are generated in the later part of the tailings include the wastewaters and We propose not to list the sludges process and thus we do not expect they fine insolubles from ore processing and collected from containment areas will contain constituents of concern at boric acid production. The tailings are around the process tanks, the loading significant levels. There is one managed in tanks and then pumped to wastewater that contains organic 31 Based on the RfD in IRIS (2E–1 mg/kg-day) and on-site evaporation ponds/surface constituents not found in the influent a 90th percentile drinking water intake rate in impoundments. The boric acid gangue brine (formaldehyde and fuel children (64 mL/Kg/day). which includes clay, sand and other

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00029 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55712 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules course insolubles, is produced during transferred to a solid waste bin in product by reinserting the off- the separation of solids from the borate preparation for on-site disposal in a specification product back into the liquor, a step the facility calls industrial Subtitle D landfill. process where it originated, without ‘‘classification.’’ The gangue is placed In addition to the above wastes, the reclamation, the off-specification on a slab for drainage and then managed facility also produces off-specification product would not be a solid waste. in on-site waste piles with gangue product that is put directly back to the The facility made beneficiation produced from the other production production process. Because the exemption claims under the Bevill process at the facility. The drainage material is reused on-site in production amendments for the tailings and gangue from the slab is sent to the tailings units in ways that present low potential wastes. Because we propose not to list ponds. The remaining wastestream is for release, and because we evaluated these wastes, we did not review the comprised of the filters from the process waste generated after the facility’s Bevill exemption claims. filtration of the borate liquor to remove secondary material is reinserted into the How Are the Wastes From the Kernite any remaining insoluble ore material process, we do not believe that the off- Ore Process Currently Managed? prior to crystallization. The filter aid is specification product presents washed off weekly and managed with significant risks. Note that, when Table III–7 summarizes our the tailings. The spent filters are facilities process off-specification information about these wastes:

TABLE III±7.ÐBORIC ACID: KERNITE ORE PROCESS WASTES

Waste category 1998 volume Sequential management practices

Tailings ...... Up to 750,000 gallons/day1 ...... (1) Stored in tank; (2) Pumped to evaporation ponds/surface im- poundments. Gangue ...... Portion of 900,000 MT2 ...... (1) Placed on slab for drainage; (2) Trucked to on-site waste piles. Spent filters ...... 3 ...... (1) Stored in solid waste bin; (2) On-site industrial Subtitle D landfill. 1 Capacity volume for boric acid surface impoundments. Current daily quantity is lower. Source: California Regional Water Quality Control Board permit, board order 6±93±17. 2 The boric acid coarse gangue is co-mingled with gangue from the other production process at the facility. That process is outside the scope of the consent decree. The boric acid gangue represents only a minor proportion of the total 900,000 tons of gangue typically deposited annually on the waste piles. Source: California Regional Water Quality Control Board permit, board order 6±93±17.

What Is EPA’s Decision About Whether potential release from the facility’s and the affinity of these constituents to To List These Wastes as Hazardous? evaporation ponds unlikely. bind with soil.33 The area under the The groundwater under the off-site facility has several geologic faults that For the reasons set out below, we area of land closest to the waste act as groundwater barriers. The South propose not to list any wastes from the management units is not suitable for use Borax fault is likely to prevent any kernite ore process for the production of as drinking water. The ore body, which potential release from the waste boric acid. is the raw material for the process, has management units from reaching the (1) Tailings. We propose not to list the a localized impact on the groundwater drinking water source for the existing tailings from boric acid production. The in its vicinity. Monitoring wells in the community well. The fault is located tailings are managed in a tank and then area show that the groundwater in the just south of the waste management pumped to evaporation ponds. The geologic strata underneath the off-site units, between the units and the well. In facility provided TCLP data for the area adjacent to the waste management addition, the groundwater underlying tailings. Those data show waste units has total dissolved solids (TDS) the waste management units is contains arsenic and antimony above levels in excess of three times the contained in the tertiary soil layer health-based drinking water levels. The maximum level for an aquifer to be whereas the community well draws Agency also assumed that boron was considered a drinking water source in from the quaternary layer. We believe present in significant levels due to the California.32 Additional factors such as that migration between these two layers nature of the ore. The facility provided low flow rate and high treatment cost would be limited. (The facility total levels for the boron concentration make the potential for a private well in submitted a detailed summary of the in the waste. We conducted an in-depth that area highly unlikely. Municipalities geologic conditions at the site. This review of the groundwater conditions at can tap into an alternative water source information has been placed in the the site and have concluded that a through a regional pipeline and need docket for this rulemaking. See groundwater exposure pathway does not not rely on groundwater. ‘‘Summary of Boron Operations exist. No one is currently living near the The geology of the area has several Hydrogeology, Potential Groundwater facility boundary closest to the waste characteristics that reduce the potential Receptors and BAP Waste Management management unit areas and it is for releases from the impoundments Parameters’’). Finally, we note that the unlikely that future development will from reaching known drinking water impoundments in question are designed occur. The closest existing drinking sources. The transport time to with a triple liner and leachate water well is two miles away from the groundwater for the constituents of collection system, making any waste management units. It is a concern appears to be significant given significant release less likely over the community well and is subject to all the depth to groundwater under the active life of the units. Based on these applicable drinking water standards. In waste management units (170–220 feet) factors, we do not believe there is a addition, there are several factors described below which make 32 California Water Quality Control Plan for the 33 Source: California Regional Water Quality contamination of this well from a Lathontan Regions, revised 1991 (p. 4.6–1) Control Board permit, board order 6–93–17.

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00030 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules 55713 groundwater exposure pathway from the groundwater would come from the unacceptable levels of risk from the tailings. tailings because there is any liquid antimony and boron in the gangue. After We also assessed the potential for air associated with the gangue would assessing possible risks from arsenic, we releases from the tailings ponds. evaporate before leaching into the compared the ratios of the waste Because the constituents of concern subsurface. Based on our decision concentrations for the three constituents from this process are nonvolatile metals, regarding the tailings, we did not further to the ingestion health-based level for we are not concerned with releases evaluate the risks to groundwater from each constituent. This ratio for arsenic through volatilization. Although the the gangue. was an order of magnitude higher than surface impoundments are evaporation We did assess in more detail the the ratios for antimony and boron, ponds, the facility claims that there is potential for air releases from the waste indicating that the highest potential risk still some level of moisture in the ponds pile. We do not expect releases of the from ingestion would arise from the at all times, thereby minimizing release nonvolatile metals from this waste. The arsenic. Thus, based on the lack of of particulates to the air. The moist gangue solids are trucked to on- significant risk for arsenic in this waste, particulates would not likely be subject site waste piles. The gangue contains the Agency concluded that neither to wind blown erosion due to the enough sodium sulfate to cause the antimony nor boron pose a significant moisture level of the waste. gangue piles to set up like cement when air risk at this site. In addition, as Furthermore, the closest off-site it dries, helping prevent erosion and air mentioned above in the tailings section, receptors are at least two miles away release of particulates from the pile. As the facility has conducted an air risk from the unit. Due to dispersion, it is a further check of potential air releases, assessment. The document shows no unlikely that any particulate releases we examined the potential for release of significant risk from the management would reach such receptors at the constituent of most concern, arsenic. practices for the gangue waste pile. The significant levels. The facility also According to data provided by the facility’s risk assessment is available in provided a risk assessment which facility, the total levels of arsenic in the the docket for today’s proposal. assessed the air risks from the tailings gangue vary between 25 and 78 mg/kg. Therefore, based on all of these factors, ponds. Their assessment did not show We compared these total concentrations we propose not to list the gangue from any air risks from the tailings ponds to one of the levels calculated as part of the production of boric acid using the even when they assumed a conservative the EPA’s Air Characteristic Study (530– kernite ore process. dry down process for the unit. (The R–99–019b, Aug 1999, Table 4–3). The (3) Spent filters. We propose not to facility’s air risk assessment is available Study evaluated different waste list the spent filters generated during the in the RCRA docket for today’s management and receptor scenarios to filtration step of the boric acid proposal). determine waste concentrations that production process. The spent filters are In summary, there are several site would remain below a specific target stored in a solid waste bin and then specific factors that need to be taken risk. Using the waste pile scenario at a managed in an on-site industrial into account when evaluating risks from receptor distance of 150 meters, the Subtitle D landfill. The filtration step this waste. This is the only facility in study showed that arsenic levels of occurs late in the process, so we expect the country producing boric acid from 6,000 ppm did not cause exceedences of minimal contamination. In addition, ore. The facility is tied to its location the target risk levels. The concentration because the filters are washed weekly, because it is the source of the ore. The levels in the gangue are well below this the vast majority of any contaminants hydrogeology of the site is such that number. In addition, the location of the filtered out at this stage would be local groundwater is not suitable for facility is remote with the closest captured by the wash process and drinking water use, and any potential residence two miles away, which is managed with the tailings (see section releases from the unit would be unlikely significantly beyond the 150 meter (1) above for listing determination on to migrate to any drinking water source. range. The Air Characteristics Study the tailings). The facility applies a daily Furthermore, the facility is remote with only evaluated direct risks from cover at the landfill which protects the nearest receptors two miles away. inhalation, not indirect risks. However, against residual particulates from being Based on all of these facts, we propose due to the desert environment where the released into the air. Furthermore, the not to list the tailings from the kernite facility is located, risks related to quantity of spent filters is relatively ore process for the production of boric consumption of soil, plants or animals small (3 MT), making it unlikely to acid. are highly unlikely to arise. Based on present a significant risk in the landfill. (2) Gangue. We propose not to list the these factors, we believe that the arsenic Finally, the location of the facility is gangue generated during the boric acid levels in the gangue do not present remote with the closest residence being process. Initially, the gangue is placed unacceptable risks via the air pathway. two miles away. Therefore, we propose on a slab to drain. The drainage from the In addition to arsenic, boron and not to list the spent filters from the gangue is collected and managed with antimony are the two other constituents kernite ore process for the production of the tailings (we assessed the drainage as of concern present in the gangue. Based boric acid. part of the tailings wastestream; see on data provided by the facility, section (1) above for our listing antimony is found at total 4. Cadmium Pigments recommendation). The drained gangue concentrations ranging from 36 mg/kg to a. Summary. We propose not to list is trucked to on-site waste piles. The 84 mg/kg in the gangue. The facility any wastes from the production of gangue is wet when transported to the estimated the boron total concentration cadmium pigments. All of the non- waste pile but most of the moisture levels to be 25,000 ppm based on wastewater residuals consistently evaporates quickly in the dry desert average daily sampling of the gangue. exhibit the toxicity characteristic for environment. The same geological Arsenic is the most toxic of the three barium, cadmium, and selenium. There conditions apply to the gangue waste constituents. Because the particulate is only one producer, and over the past unit as described above for the tailings releases and exposure scenario would seven years the producer has drummed waste unit. The gangue is ultimately likely be the same for all three and shipped with manifests all its non- managed as a dry waste pile and there constituents and because, as discussed wastewater residuals to an off-site is virtually no precipitation to cause above, we do not believe arsenic poses Subtitle C facility for treatment to leaching. We assumed a greater risk to a concern, we also believe there are no applicable LDR standards. The

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00031 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55714 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules wastewaters are pretreated on-site in and protective coatings for plastics, limited to the manufacturing areas closed tanks prior to discharge to a glass, ceramics, rubber and other requiring use of cadmium pigments, POTW, which is regulated under the materials. The coatings provide heat such as the plastics industry, where no Clean Water Act. We conclude that the resistance to surfaces and a barrier to substitute is adequate. Our RCRA existing regulatory controls adequately chemical and sunlight exposures. Section 3007 Survey results show that reduce risks, and there are no exposure Cadmium pigments are produced by six out of seven facilities ceased pathways of concern. These wastes do digesting cadmium metal in sulfuric production of cadmium pigments in not pose a substantial present or acid, nitric acid, and water to produce recent years. The domestic demand for potential hazard, and thus do not meet a cadmium sulfate solution (liquor). cadmium pigments in the next few years the criteria for listing set out in 40 CFR Chemical reagents are added to the is likely to remain stable. A more 261.11(a)(3). liquor to selectively precipitate out complete discussion of this process and b. Description of the cadmium metals which are present as impurities. the industry is provided in the pigments industry. One facility Sodium sulfide and metals (e.g., zinc, ‘‘Cadmium Pigments Listing produced cadmium pigments in the selenium) are added to the purified Background Document for the Inorganic United States in 1998 and 1999. liquor to yield a slurry which, after Chemical Listing Determination’’ in the Cadmium pigments are cadmium filtration, is the ‘‘greencake’’, the first docket for today’s proposal. sulfides of variable composition, usually intermediate product from the cadmium b. What kinds of wastes are generated produced as powders but also available pigments production. The greencakes by this process?. Using the facility’s in other forms such as pastes and are then washed, sized, and calcined. survey response, we divided the wastes liquids. Cadmium pigments are used to The calcined materials are ground, into two broad categories: Wastewaters provide shades of bright yellow, orange, rewashed, filtered, dried, milled, and and non-wastewaters. Table III–8 red, and maroon. The shades depend on blended to make different shades. summarizes the types of wastes in each the ratio of cadmium and zinc to The use of cadmium pigments is category, the characteristics of each sulfides and selenium. Current uses of declining.34 Growth in the overall waste, waste volume, and current cadmium pigments include decorative demand for cadmium pigments is management practices:

TABLE III±8.ÐCADMIUM PIGMENT PRODUCTION WASTES

Reported 1998 waste Waste category waste volume Management practice codes (MT)

Non-wastewaters

Miscellaneous solid wastes, including materials from D005 33.5 ...... Each waste is drummed (separately or sometimes dust collectors, plant cleanup, filtered pigments from D006 combined) and shipped to a commercial off-site the presses, and from the on-site wastewater pre- D010 hazardous waste treatment facility to be treated and treatment process. decharacterized before placing in a Subtitle D land- fill. Note: D005Ðbarium D006Ðcadmium D010Ðselenium Contaminated paper and cloth, including filter bags, fil- D005 9.3 ter cloths, filter cartridges, and dust collector bags. D006 D010 Contaminated gaskets generated from the red and yel- D005 0.3 low calciners. D006 D010 Iron press residue generated from digestion of cad- D005 4.5 mium metal. D006 D010

Wastewaters

Gas scrubber wastewater (spent caustic from scrub- Not reported ..... pH adjusted, treated to re- All these wastewaters are bing vapors generated from calcination process). move zinc and cad- then combined and fur- mium. The resulting ther treated in on-site sludge is a part of the closed tanks for pH ad- miscellaneous solid justment; 2-step filtra- wastes. tion; monitoring for tur- bidity prior to discharge to a POTW. Process wastewater from filtering the greencake ...... Not reported ..... pH adjusted, treated to re- cover cadmium. Process wastewaters from wet washing system ...... Not reported.

34 minerals.usgs.gov/minerals/pubs/commodity/ USGS Minerals Information, Mineral cadmium/140396.txt) Commodity Summary, 1996 (see http://

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c. Agency evaluation. After evaluating production wastes. The landfill waste management practices and the characteristics and current information and leachate data are potential exposure pathways, we management practices of all the waste provided in the ‘‘Cadmium Pigments concluded that there are no risk residuals, we determined that: (1) all the Listing Background Document for the pathways of concern. These wastes do non-wastewater wastes are being Inorganic Chemical Listing not meet the criteria set out at 40 CFR properly treated and managed as Determination’’ in the docket for today’s 261.11(a)(3) for listing as hazardous. hazardous wastes under RCRA proposal. We recognize that the residues They do not pose a substantial present regulations, and (2) all the wastewaters from commercial treatment facilities or potential hazard to human health or are being treated on-site in closed tanks represent the commingling of wastes the environment. and discharged to a permitted POTW, from a variety of facilities and wastes. b. Description of the inorganic where they are subject to the Clean Therefore, information on the landfill hydrogen cyanide industry. Hydrogen Water Act. Therefore, we did not pursue leachate from treated material is of cyanide (HCN) is used in the risk assessment modeling for any of limited use. However, the data available manufacture of a number of important these wastes. The following are the indicate that the cadmium pigment chemicals including: adiponitrile to details of our evaluation: wastes do not present a substantial produce nylon, methyl methacrylate to (1) Non-wastewaters. In its RCRA hazard when disposed. Given that the produce clear acrylic plastics, sodium Section 3007 Survey, the facility generating facility has followed the cyanide for the recovery of gold, classified all four wastes of this category reported management practice for seven triazines for agricultural herbicides, as characteristic hazardous, as years, we believe use of this or methionine for animal food generated, for barium, cadmium, and comparable treatment and disposal will supplements, and chelating agents for selenium. The facility also provided continue. water treatment. data characterizing each non-wastewater HCN is manufactured via two primary What Is EPA’s Listing Rationale for inorganic synthesis processes: residual for total and TCLP These Wastes? ¨ concentrations of eight TC metals. Andrussow and Blausaure-Methan- Except for chromium (which was We propose not to list any of the four Ammoniak (BMA). The Andrussow detected in the TCLP leachate of one wastes in this category as hazardous process involves the reaction of waste below its health-based level), no because they are already managed in ammonia, methane (natural gas) and air other hazardous constituents were compliance with existing hazardous over a platinum catalyst; the BMA reported. The total volume of these four waste regulations, including full process is similar except the reaction wastes was 47.6 metric tons in 1998. compliance with the BDAT occurs in the absence of air. The Over the past seven years the requirements for treatment prior to land reaction products are quenched with generator has managed all its non- disposal. We conclude that available water. Excess ammonia reactant is wastewater wastes generated from the data on the specific cadmium pigment recovered for reuse in the reaction or production of cadmium pigments as TC manufacturing wastes do not support a converted to an ammonium salt. The hazardous wastes. These wastes are decision to list the wastes as hazardous. aqueous HCN product is purified and (2) Wastewaters. We propose not to drummed and shipped with manifests concentrated for use as a liquid list the wastewaters as hazardous to a commercial off-site Subtitle C feedstock for manufacturing of one or because the gas scrubber and the facility for treatment. The off-site more of the final products mentioned process wastewaters are pretreated on- treatment includes mixing and treating above. Two of the Andrussow process site in closed tanks prior to discharge to the wastes with other solid wastes and manufacturers do not produce a liquid a POTW. The wastewater treatment the addition of lime and fly ash to meet hydrogen cyanide intermediate product tanks provide sufficient structural but immediately convert the hydrogen the current LDR treatment standards integrity to minimize potential releases cyanide in the reactor gases in a sodium (via stabilization). The resultant mixture to groundwater. We are unlikely to find hydroxide contactor to produce liquid forms a concrete-like residue, which no potential air releases from these tanks as sodium cyanide. longer exhibits a characteristic and is neither volatile contaminants nor There are ten manufacturers of managed in a Subtitle D landfill. We airborne particulates are likely to be hydrogen cyanide in the United States believe this management, which present in these wastewaters. During who use the Andrussow or the BMA complies with existing Subtitle C treatment, the closed tanks present no process. Of these ten manufacturers, regulations, adequately protects human significant threat of release to the only one uses the BMA process. Two of health and the environment. environment. After treatment, the the nine Andrussow manufacturers use Although we generally believe that an abbreviated version of the Subtitle C regulations for characteristic wastewaters are subject to the Clean Water Act program. We conclude that Andrussow process to produce sodium wastes adequately prevent cyanide. Manufacture of sodium mismanagement, we have additional the wastewaters do not warrant listing. We assessed solids from the on-site cyanide as a final product results in data that help confirm our conclusion fewer wastes and significantly lower for this waste. The landfill information treatment as miscellaneous wastes discussed above in section (1). wastewater volumes. and leachate data provided by the local The inorganic hydrogen cyanide and state governments (per our request) 5. Inorganic Hydrogen Cyanide industry subject to this rulemaking is indicate that the landfill has a liner with a. Summary. We propose not to list composed only of the facilities that a leachate collection system. The any wastes from the production of produce hydrogen cyanide as an 35 landfill leachate data we have to date inorganic hydrogen cyanide (HCN) as intermediate product or feedstock to demonstrate that constituents detected hazardous under Subtitle C of RCRA. manufacture a variety of commercial in the landfill leachates are not These wastes are managed in on-site chemicals using the Andrussow and attributable to the cadmium pigments wastewater treatment processes, BMA processes. This proposal industrial landfills, municipal landfills, specifically does not cover wastes from 35 Quarterly leachate monitoring data from March 95 to September 98, provided by Michigan’s hazardous waste incinerators, hazardous the manufacturing of HCN as a Department of Environment, Wayne County District waste landfills, and hazardous waste byproduct in the manufacture of Office and Local Office. injection wells. After analysis of these acrylonitrile by the ammoxidation of

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00033 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55716 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules propylene (Sohio process). The Sohio natural gas prior to being used as solids are generated during manual process is inherently an organic process feedstock. tank cleaning after thorough washing. chemical manufacturing process, and is —Process air cartridge filters. This —Wastewater filters. These are not within the scope of the inorganic waste consists of spent filter material generated from the filtration of chemicals manufacturing industry or and filter solids that are generated process wastewater prior to deep-well the consent decree. Furthermore, we during the filtration of ambient air injection. have already evaluated wastes for that is used in the reaction. —Ammonium sulfate filters. This waste acrylonitrile manufacturing, and the —Acid spray cartridge filters. The waste is from the filtration of the cyanide wastes associated with the consists of spent filter cartridges and ammonium sulfate solution from the Sohio process (K011, K013, and K014) filter solids from acid spray filters neutralization of excess ammonia by are subject to Subtitle C regulation. used in the hydrogen cyanide sulfuric acid. The filtered ammonium c. What kinds of wastes are generated stripper. sulfate solution is then crystallized by this process? —Spent catalyst. This waste consists of into solid form prior to sale as metal gauze panels that contain the fertilizer. How Did We Categorize the Wastes? precious-metal catalyst used to —Spent ammonium phosphate. Wastes generated from the production catalyze the synthesis reaction. The Ammonium phosphate solution is of hydrogen cyanide consist of various catalyst activity diminishes with time used to scrub the off-gas from the types of wastewater, various types of and needs to be replaced with fresh reactor to assist in ammonium spent filter media, spent catalyst, catalyst periodically. recovery. biological solids from wastewater —Ammonium sulfate and ammonium —Organic layer from wastewater treatment, and ammonium salts. Based phosphate. The ammonium wastes are collection tank. This is generated from on an assessment of the wastes reported generated from the neutralization of the treatment of commingled HCN in the survey, the wastes were excess ammonia in the process using wastewater and predominantly non- categorized as follows: sulfuric or phosphoric acid. HCN process wastewater. —Commingled wastewaters. This waste —Miscellaneous wastewaters. These In addition to these wastes, other includes continuously generated numerous wastewaters are generated residuals are produced by some of the wastewaters such as HCN purification during plant upsets or shutdowns for facilities that are recycled back to the wastewater and ammonia purification maintenance and are reported in production process. These materials wastewater. detail in the ‘‘Inorganic Hydrogen consist of process water and recovered —Ammonia recycle cartridge and spent Cyanide Listing Background ammonia. These residuals are reused carbon filters. This waste consists of Document for the Inorganic Chemical on-site via enclosed piping systems and spent filter material and filter solids Listing Determination.’’ tanks, minimizing the potential for that are generated during the filtration —HCN polymer and sump wastes. environmental releases. Also, we of the recycled unreacted ammonia These wastes are generated in process evaluated all wastes generated after stream prior to being reused as vessels, tanks, and wastewater these secondary materials are reinserted process feedstock. collection sumps and removed during or reused; we do not believe that these —Biological wastewater treatment periodic plant maintenance secondary materials present significant solids. The are generated operations. risks. Consequently, we did not evaluate from the biological treatment of —Sludge from wastewater collection them further. process and non-process wastewaters tank. This waste is generated from the to remove residual cyanide and settling of suspended solids in How Are These Wastes Currently Being organonitrile contaminants. wastewater tanks and removed during Managed? —Feed gas cartridge and spent carbon periodic plant maintenance Table III–9 summarizes the major filters. This waste consists of spent operations. waste categories, waste characteristics, filter material and filter solids that are —HCN storage tank solids. These solids waste volumes, and their current generated during the filtration of settle out of the HCN product. The management practices:

TABLE III±9.ÐINORGANIC HYDROGEN CYANIDE PRODUCTION WASTES

Waste Category Reported 1998 (Number of facilities) Waste volume Management practices Codes 1 (MT)

Commingled wastewaters (8) ...... D002 ...... 5,600,000 On-site wastewater treatment in tanks or surface impoundments, dis- charge to NPDES outfall or POTW. Ammonia recycle cartridge and spent carbon filters (5) ...... none ...... 73 Off-site municipal D landfill; off-site in- dustrial D landfill; on-site Subtitle C landfill; on-site Subtitle C inciner- ation. Biological wastewater treatment solids (4) ...... none; 45,397 Off-site industrial Subtitle D landfill; F0393. off-site municipal Subtitle D landfill; on-site Subtitle C landfill. Feed gas cartridge and spent carbon filters (9) ...... none ...... 9.7 Off-site municipal D landfill; off-site in- dustrial D landfill; on-site Subtitle C landfill as non-hazardous waste; off- site recycle/reuse via return to man- ufacturer. Process air cartridge filters (8) ...... none ...... 7.5 Off-site municipal D landfill; off-site in- dustrial D landfill; reclamation.

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TABLE III±9.ÐINORGANIC HYDROGEN CYANIDE PRODUCTION WASTESÐContinued

Waste Category Reported 1998 (Number of facilities) Waste volume Management practices Codes 1 (MT)

Acid spray cartridge filters (1) ...... none ...... 1.1 On-site Subtitle C landfill as nonhaz- ardous waste. Spent catalyst (10) ...... none ...... 4.06 Off-site reclamation. Ammonium sulfate and ammonium phosphate (3) ...... none ...... 27,425 Off-site use as fertilizer. Miscellaneous wastewaters (4) ...... none ...... 209,000 Managed with commingled wastewaters described above. HCN polymer and sump wastes (1) ...... none ...... 0.7 Off-site industrial D landfill Sludge from wastewater collection tank (2) ...... D001;D018 23.9 Stabilization/off-site Subtitle C landfill; off-site Subtitle C . HCN storage tank solids (1) ...... none ...... 0.3 Off-site municipal D landfill Wastewater filters (1) ...... none ...... 450 Captive off-site Subtitle C incineration. Ammonium sulfate filters (1) ...... none ...... 1.1 Off-site industrial D landfill Spent Ammonium Phosphate (1) ...... none ...... 230 On-site reuse as biological treatment system nutrient source or on-site nonhazardous waste incineration Organic layer from wastewater collection tank (1) ...... D001 ...... 43.3 Off-site Subtitle C incineration (1993) 1 D001 (ignitability), D002 (corrosivity), D018 (benzene). 2 Includes 2.1 MT reported for 1993. 3 One facility commingles wastewater to generate a hazardous waste derived from F039 wastewater.

d. Agency evaluation. We selected commingled wastewaters by filtration impoundments in question would not three facilities in Alabama, Tennessee, and disposal via deepwell injection. be moved off-site or to different locations. and Texas to collect record samples of What Management Scenarios Were wastes for the listing determination. Assessed? Our decision on what scenario to These facilities were selected based on assess was based on review of our the survey information for the entire Based on the reported management practices, we assessed the potential for analytical data and the characteristics of industry sector and collectively the surface impoundments used at the represent all the wastes generated and releases from tanks and surface impoundments. We decided that risks three facilities. We evaluated the all of the waste management practices potential for groundwater releases to used by the manufacturing sector. from the ultimate discharges to NPDES outfalls and POTWs are adequately drinking water wells at the Alabama (1) Commingled wastewaters. controlled by the Clean Water Act. Risks site, and potential surface water impacts from discharges to Class I injection at the Tennessee facility. The analytical How Many Facilities Generate This data for the wastewater managed in the Waste Category and How Is It Managed? wells with RCRA ‘‘no-migration’’ variances are adequately regulated surface impoundment at the Texas Eight of the ten facilities generated under the Safe Drinking Water Act and facility showed that all levels of the commingled wastewaters from the RCRA (see section III.D.3). toxicants of concern are below health- inorganic hydrogen cyanide process. Potential releases to groundwater. We based levels, or are associated with The total volume of commingled assessed both the tank and surface other commingled on-site production wastewaters reported by these facilities impoundment scenarios for potential processes and are not due to HCN was 5.5 million MT in 1998. Six of these releases to groundwater and determined production. eight facilities treat the commingled that the unlined surface impoundment The Alabama facility manages wastewaters using one or more of the scenario poses a more significant wastewater in a series of surface following operations in their on-site potential risk to groundwater than the impoundments and tanks that provide wastewater treatment processes: (a) tank scenario. We focused on the equalization, oxidation, maturation, steam stripping to remove cyanide and surface impoundment pathway because rock-reed filtration, and mixing. In ammonia, with off-gasses vented to several of the reported surface addition, the facility has an emergency flares, scrubbers or incinerators; (b) pH impoundments are unlined, posing a holding basin which has also been used adjustment; (c) aerated or non-aerated potential direct release pathway to for HCN process wastewaters. The biological treatment in tanks or lined/ groundwater. We take the position that surface impoundments are equipped unlined surface impoundments; (d) tanks, by the impervious nature of the with double synthetic liners with ozone treatment in tanks; (e) construction materials (concrete, leachate detection and collection oxychlorination in surface fiberglass, or steel) are not likely to systems. The oxidation basin is a impoundments; (f) settling in surface result in significant releases to concrete-lined structure with an impoundments; and NPDES outfalls, or groundwater. We conducted sampling additional synthetic liner. Our POTWs. In addition to commingling of and analysis of these wastewaters at the analytical data indicates that the hydrogen cyanide process three facilities located in Alabama, concentrations at the inlet to the wastewaters, some facilities also Tennessee, and Texas currently using impoundments would exceed the HBLs commingle these wastewaters with surface impoundment-based wastewater for one constituent of concern wastewaters from other non-HCN treatment systems. We assessed each (acetonitrile). A study of existing wells processes generated in the same site individually, because we believe it near the facility indicates the presence chemical manufacturing complex. The is reasonable to assume that large of private water wells within a one-mile remaining two facilities manage their volume wastewaters managed in radius of the property boundary. We

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Despite the criteria, thus, we assessed this facility’s wastewaters in the equalization estimated nature of the results for impoundments for potential releases to impoundment. We estimated the acetonitrile in this waste sample, the groundwater. As described below, the concentration of the constituents of data clearly indicate that acetonitrile is Tennessee facility and its surface concern in the equalization likely to be present in the waste. impoundments are sited on the banks of impoundment by applying the dilution Acetonitrile, also commonly referred to the Loosahatchie River, with no off-site factor in the impoundment (e.g., 36 to as methyl cyanide, is a likely by-product downgradient wells. However, we did 1 total wastewaters to HCN from the main reaction between assess the impact from potential releases wastewaters), and we assessed these methane and ammonia to form to groundwater to the nearby river at concentrations in our modeling for this hydrogen cyanide. In addition, samples this site. pathway. For the groundwater-to- we collected at the Tennessee facility surface water pathway at the Tennessee show that significant levels of Potential releases to air. We also facility, we used the sample collected at examined the air exposure pathway for acetonitrile are present in the the exit from the surface wastewater, albeit at somewhat lower the wastewater treatment impoundments. We used the sample impoundments and tanks because of the levels than we found at the Alabama from wastewater exiting the unit, rather site. potential release of volatile organic than at the inlet, because treatment compounds and hydrogen cyanide from occurs in the impoundment. However, We initially sampled at the Tennessee the wastewater treatment units. EPA is the inlet data are similar, and even facility in August of 1999 (sample DM– developing maximum achievable using the inlet data would not 1–HC–08). We used the analytical control technology (MACT) standards significantly increase the surface water results for this sample as input to the for cyanide manufacturing under the screening results. risk assessment (described further Clean Air Act (CAA), which may We analyzed the waste for both below). However, because our analytical address these emissions. Although this amenable and total cyanide, as well as results for amenable cyanide were rule will be technology-based, the CAA a number of volatile organics and qualified due to holding time ultimately requires EPA to regulate metals. We used the amenable cyanide exceedences, we sampled at this facility significant risks remaining after the results as our cyanide risk assessment a second time in October of 1999 to imposition of technology-based inputs because we believe that better understand the potential impact controls. EPA has also proposed amenable cyanide most closely of this waste on the environment (DM– regulations under the CAA for volatile represents the fraction of cyanide likely 2–HC–08). All of the analytical data for organic compound (VOC) emissions to be mobile in a groundwater scenario these samples are available in from wastewater at Synthetic Organic and the ‘‘free cyanide’’ assessed in our ‘‘Inorganic Hydrogen Cyanide Listing Chemical Manufacturing Industry health-based level (HBL). However, this Background Document for the Inorganic (SOCMI) facilities, which would cover had no impact on our risk results, Chemicals Listing Determination’’ in the the HCN manufacturers (see proposal at because our data show that amenable docket for today’s proposal. The second 60 FR 46780, September 12, 1994). and total cyanide results for this waste round of sampling showed lower levels Therefore, we are deferring control of are the same. of the key constituent of potential any air releases to the MACT and We sampled the wastewater at the concern than found in the first round of SOCMI standards and did not assess Alabama facility in August, 1999. The sampling. Due to time constraints, we this pathway further in today’s analytical data for the commingled HCN did not re-run the risk assessment proposal. wastewaters (DG–1–HC–07) represent model for this pathway to incorporate waste concentrations prior to the second round of analytical data. How Was This Waste Category However, this would result in somewhat Characterized? commingling with other non-HCN wastewaters. Our results for a key lower risks, and thus would have had We conducted sampling and analysis chemical, acetonitrile, are qualified as not impacted our proposed decision. of these wastewaters at the three ‘‘estimated’’ for this sample as a result The critical analytical results for the facilities currently using surface of problems during sampling and commingled wastewaters for the impoundment-based wastewater analyses at this site as described further Tennessee and Alabama surface treatment systems. We collected in Waste Characterization Report, impoundments are presented below in samples at various places in the process, Degussa-Huls; February 25, 2000, Table III–10. These represent the including prior to commingling, so that constituents found to be present in the we could assess the risks of the 36 The ‘‘Inorganic Hydrogen Cyanide Listing wastewaters at level exceeding the HBLs wastestream at issue here. Today’s Background Document for the Inorganic Chemical or AWQC. (Several other constituents proposal is based primarily on samples Listing Determination,’’ available in the docket for today’s proposal, provides all analytical data we were marginally above the AWQC and of the commingled wastewaters developed, as well as split samples collected by were not important in the surface water collected in the wastewater treatment industry, where available. screening.)

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TABLE III±10.ÐCHARACTERIZATION OF COMMINGLED WASTEWATERS FROM INORGANIC HCN PRODUCTION (MG/L)

Sample Sample DM±2±HC± Sample 1 Constituent of concern DM±1±HC± 08 DG±1±HC±07 HBL AWQC 08 2nd Rnd

Amenable CN ...... 0.638 <0.01 0.509 0.3 0.005 Nitrite as N ...... 11.5 no analysis <2.5 2 1 Vinyl chloride ...... 0.029 3 0.0066 L <0.001 0.0009 (0.1) 0.002 Acetonitrile ...... 4 50 K 28 L 190 0.09 (0.045) 2 N/A Acrylonitrile ...... 0.013 <0.001 <0.0005 0.002 (0.03) 5.9E±05 1 HBL in parenthesis based on inhalation pathway from residential use of water (e.g., showering). 2 N/A: Not Applicable. 3 L: Qualified result with a low bias for positive result. 4 K: Qualified result with a high bias for positive result.

How Was the Groundwater-To-Drinking the most likely direction of groundwater TABLE III±11.ÐGROUNDWATER RISK Water Risk Assessment Established? flow is to the low-lying areas to the RESULTS FOR COMMINGLED The Alabama facility’s surface north-northeast of the surface WASTEWATERS FROM THE PRODUC- impoundments are located in the center impoundments. We found there are TION OF INORGANIC HYDROGEN CY- of an industrial park on the west side of drinking water wells located due east of ANIDE Mobile Bay. The wastewater treatment the equalization surface impoundment. impoundments are located near the Although the wells are located east of Acetonitrile eastern property boundary of the facility the surface impoundment instead of the Percentile hazard and approximately 4,000 feet south of quotient estimated north-northeast groundwater (HQ) 1 the State of Alabama barge canal. We flow direction, they are at somewhat chose to assess surface water risks at the lower ground elevation than the surface 90th % ...... 0.3 Tennessee facility, which is closer to a impoundment. Given the uncertainty in 95th % ...... 0.5 surface water body. However, given the the direction of the groundwater flow, 1 Risk from inhalation scenario during show- use of groundwater in the area around we assumed that contaminated ering included exposure factors for both adult the Alabama facility, we assessed the groundwater from the surface and child in the analysis. possible impact on drinking water impoundment could migrate to the east wells. We selected the equalization How Was The Groundwater-To-Surface and reach these wells. Based on the basin as the unit for quantitative Water Risk Assessment Established? available land use and groundwater use modeling. This is the first surface The Tennessee facility and its surface information for this area, we performed impoundment in the series and is likely impoundments are sited on the banks of to hold the highest level of constituents risk modeling for potential releases to the Loosahatchie River. The surface of concern. We elected not to assess the drinking water wells located between impoundments are located emergency holding pond, which is used 3,100 and 5,280 feet east of the surface approximately 800 feet from the river. primarily during high stormwater impoundment. The minimum distance Based on information available in the events. Due to the intermittent use of of 3,100 feet is based on the distance Remedial Facility Investigation (RFI),38 the holding pond, we expect the from the impoundment to the eastern the direction of the groundwater flow is potential for significant groundwater boundary of the industrial area documented to be south towards the releases to be greater for the controlled by the facility. The maximum Loosahatchie River. The possibility of a equalization pond. In addition, the distance of 5,280 is the distance east public water supply well or private well equalization pond is covered with a from the impoundment to the closest being located downgradient of the floating synthetic membrane, while the known well. This drinking water well Tennessee surface impoundments is holding pond is not.37 Our modeling of appears to be located just inside the unlikely because the facility boundary the covered equalization pond did not eastern boundary of the state property, extends to the river to the south. Hence, assume any loss of the volatile which lies to the east of the industrial based on the geologic setting of the constituents of concern, thus allowing park where the facility is located. We facility as detailed above, we believe it more of the constituents to infiltrate to also assumed that a future well may be is highly unlikely that these the groundwater rather than volatilize to placed in the same State property impoundments could impact drinking the air. directly east of the facility’s water wells via migration of a Based on information available in a undeveloped tract at approximately contaminated groundwater plume. Based on these facts we did not assess corrective action plan related to a 3,100 feet from the surface product spill on-site (Risk-Based the groundwater-to-drinking water well impoundment. The details of this Corrective Action Plan for the Sodium pathway further at this site. We did, assessment are presented in the ‘‘Risk Cyanide Production Unit at Degussa however, conduct a screening analysis Assessment for the Listing Corporation Alabama Facility, of potential releases of groundwater to Theodore, Alabama; March 19, 1998), Determinations for Inorganic Chemical surface water and subsequent exposure Manufacturing Wastes’’ in the docket for via ingestion because of the proximity of 37 The facility reported that the cover on the today’s proposal. The results of the risk the unit to the river. We calculated the equalization unit was installed to ensure modeling for the only drinking water concentrations in the river that would compliance with expected new regulations to constituent of concern are presented in control volatile organic carbon emissions from result from discharge of contaminated wastewater sources for the Synthetic Organic Table III–11 below. Chemical Manufacturing Industry (SOCMI) 38 U.S. EPA Phase II RFI Workplan, (proposal, 59 FR 46780, September 9, 1994). Potentiometric Surface Plan, March 3 & 4, 1999.

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00037 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55720 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules groundwater by estimating the result in yet lower river concentrations. municipal and an industrial landfill, infiltration rate for the unlined We did not account for the likelihood using only those two waste volumes impoundment and diluting the resulting that river water would be pretreated reported to be managed in off-site leachate volume into the river under prior to use for drinking and showering. Subtitle D landfills; volumes managed various flow conditions. The results of We did not account for volatilization, as hazardous wastes were not included this screening level analysis suggest that , or hydrolysis of the in this array. No significant volatile concentrations of the constituents of cyanide and other constituents prior to constituents were detected in this waste concern in the river would be well exposure. Even if we used the surface (only non-volatile metals were detected; below the aquatic life AWQC and HBLs impoundment influent concentrations, see following section), thus rather than the exit concentrations, as for drinking water. The details of the volatilization from landfills to the air input to the analysis, this waste would screening analysis are presented in was not a pathway of concern. ‘‘Risk Assessment for the Listing not exceed risk thresholds in the Determinations for Inorganic Chemical adjacent river. We did not conduct risk assessment of Manufacturing Wastes’’ in the docket for For these reasons, we propose not to the voluntary Subtitle C landfill and today’s proposal. list this waste category as hazardous. incineration practices because we For a more complete description of this assumed that listing would not What Is EPA’s Listing Rationale for This analysis, see ‘‘Risk Assessment for the significantly increase regulatory control Waste? Listing Determination for Inorganic for these wastes. Note that these on-site Our risk assessment results for the Chemical Manufacturing Wastes’’ in the captive units have sufficient capacity surface impoundment scenario, docket for this proposal. and flexibility to accept these relatively summarized above for drinking water in (2) Ammonia recycle cartridge and small volume non-hazardous wastes. Table III–11, suggest that the only spent carbon filters. How Was This Waste Category constituent of concern that required How Many Facilities Generate This Characterized? modeling (acetonitrile) does not pose a Waste Category and How Is It Managed? substantial present or potential hazard Five facilities reported generating 73 Two samples were collected at to human health and the environment. MT/year of filter media and waste solids different facilities. We sampled again at The HQ was below one at both the 90th in 1998 from the removal of both facilities because of problems with and 95th percentile in the probabilistic organonitrile polymers from the the cyanide analyses for the first set of risk distribution. ammonia recycle stream. The analyses and elevated detection limits The results of our risk analysis also management methods reported by the for certain metals in the Tennessee show that hypothetical releases to the industry were off-site municipal sample. Due to the schedule constraints adjacent river would not result in Subtitle D landfill, off-site industrial of this determination, we initiated the exceedences of risk thresholds. Our Subtitle D landfill, on-site Subtitle C risk analyses using the first round of analysis was conducted at a screening incineration, and on-site Subtitle C samples. The risk analysis and second level and thus is based on a number of landfill. conservative assumptions that may round of sampling and analysis were overstate actual risk. We did not What Management Scenarios Were conducted in parallel. HBLs are shown account for dilution of the potential Assessed? in Table III–12. plume in groundwater flowing under We conducted risk assessment the surface impoundment that would modeling for off-site disposal in both a

TABLE III±12.ÐCHARACTERIZATION OF AMMONIA RECYCLE FILTERS [mg/L]

RH±1±HC±05 (1st RH±2±HC±05 (2nd DM±1±HC±04 (1st DM±02±HC±04 (2nd Parameter data set) data set) data set) data set) HBL TCLP SPLP TCLP SPLP TCLP SPLP TCLP SPLP

Antimony ...... 1 0.55 J 0.59 <0.5 0.237 <0.5 <0.5 0.8 0.08 0.006 Arsenic ...... 2 0.045 L 0.039 <0.5 0.0137 <0.5 <0.05 <0.5 0.0112 0.0007 Nickel ...... 0.50 J 0.61 <0.2 0.303 <0.2 0.0654 <0.2 0.0178 0.31 Total CN ...... N/A 2.4 L 0.230 0.243 0.218 0.187 L 3 0.222 0.303 4 0.31 1 J: Estimated result, due to poor field duplication. 2 L: Qualified result with a low bias for positive result. 3 Average of duplicate sample results. 4 HBL for hydrogen cyanide.

How Was the Groundwater Ingestion the wastes are reported to be managed. constraints of this listing determination, Risk Assessment Established? As noted in section III.C., we used the we could not delay the risk assessment TCLP results for the municipal landfill modeling until the validated results of We assessed the off-site landfill scenario and the SPLP for the industrial the second round of analyses became scenario for the ammonia recycle filter landfill scenario. available, and thus used the first round cartridges, reflecting the types of of samples for the Texas facility as management reported for this waste. We As described above, we had some assessed the groundwater ingestion initial concerns about our analytical model input. Subsequently, having pathway for these landfills. Our model data and determined that re-analysis reviewed all the analytical data, we inputs included different hydrogeologic would serve to demonstrate the validity believe that the modeled data set settings reflecting the two regions where of these data. Due to the time appropriately characterizes the risks of

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00038 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules 55721 all constituents included in the first What is EPA’s Listing Rationale for This exceeded one. As a matter of policy, we sampling round, and that re-running the Waste? generally do not consider listing wastes model with the second round of The results of our probabilistic risk with predicted cancer risks of less than analytical data would not increase the assessment are provided in Table III–13 1E–06 or hazard quotients of less than predicted risk. The only additional below (we also completed deterministic 1.0. We see no special concerns constituent of concern found in the risk modeling and the results were warranting an exception to this policy. second analysis was cadmium. We comparable; see ‘‘Risk Assessment for Based on these results we conclude that modeled this constituent using the same the Listing Determinations for Inorganic this waste does not pose risk to human two scenarios and found no significant Chemical Manufacturing Wastes’’ for health and the environment at levels risk. details). At the 90th and 95th percentile that warrant listing. We therefore are cumulative risk level, we found no proposing not to list ammonia recycle cancer risk in excess of 1E–07, nor did filters from inorganic hydrogen cyanide we find any hazard quotients that production.

TABLE III±13.ÐGROUNDWATER RISK RESULTS FOR AMMONIA RECYCLE FILTERS 1

Antimony Arsenic Cadmium Percentile Adult cancer Child cancer Adult HQ Child HQ risk risk Adult HQ Child HQ

Industrial Landfill: 90th ...... 7.9E±02 1.6E±01 3.8E±08 2.8E±08 3.6E±04 7.7E±04 95th ...... 1.9E±01 3.9E±01 1.6E±07 1.2E±07 1.6E±03 3.4E±03 Municipal Landfill: 90th ...... 8.7E±02 1.8E±01 3.9E±08 3.1E±08 4.0E±04 8.5E±04 95th ...... 2.0E±01 4.2E±01 1.8E±07 1.3E±07 1.7E±03 3.7E±03 1 Modeling for two other constituents (nickel and cyanide) yielded HQs that were extremely small (<1E±16) even at the 95th%.

(3) Biological wastewater treatment leaching results to the HBLs. In all cases off-site municipal D landfill, off-site solids. the SPLP and TCLP levels industrial D landfill, and on-site C corresponding to the management hazardous landfill. The facility using How Many Facilities Generate This practice were below the HBLs. the hazardous C landfill for disposal of Waste Category and How Is It Managed? For the agricultural liming scenario, the filters is managing the filters as Four facilities reported a total volume we compared the total concentrations in nonhazardous waste in a captive on-site of 45,397 MT/year for this waste. The the waste to the soil screening levels; no C landfill. management methods reported are off- constituents exceeded these screening site municipal and industrial Subtitle D levels, i.e., all constituents were below What Management Scenarios Were landfills, on-site Subtitle C landfill, and background or direct soil ingestion Assessed? off-site use as agricultural liming agent levels. We assessed the municipal and (volume not reported). The full analyses are summarized in industrial Subtitle D landfill scenarios What Management Scenarios Were the ‘‘Inorganic Hydrogen Cyanide using our TCLP and SPLP results, Assessed? Listing Background Document for the respectively. No volatile constituents Inorganic Chemicals Listing were detected in this waste (only non- We evaluated the Subtitle D landfill Determination’’ and the analytical volatile metals were detected; see and the agricultural liming agent results are reported in detail in the following section), thus volatilization scenario reflecting the reported Waste Characterization Reports for this management practices. We assessed the from landfills to the air was not a sector; these documents are available in pathway of concern. We did not assess landfill scenario using our TCLP and the docket for today’s proposal. SPLP results for the wastes reported the voluntary Subtitle C landfill managed in such landfills. We assessed What Is EPA’s Listing Rationale for This scenario because we assumed that the agricultural use scenario by Waste? listing would not significantly increase regulatory control. Note that the on-site comparing total constituent We propose not to list this waste as unit has sufficient capacity to continue concentrations to the soil screening hazardous because the levels of toxicant to accept this small volume waste. levels (see section III.C.3). constituents found in the waste are How Was This Waste Category below the levels of concern. How Was This Waste Category Characterized? (4) Feed gas cartridge and spent Characterized? carbon filters. We collected two samples of this We collected one sample of this waste at two different facilities. We How Many Facilities Generate This waste. The analytical results showed conducted total and leaching analyses of Waste Category and How Is It Managed? that SPLP levels for all constituents are these samples. To evaluate the Nine facilities reported a total volume below drinking water HBLs. The TCLP industrial landfill disposal scenario we of 9.7 MT/year for this waste. The results showed levels that exceeded compared the SPLP leaching results to management methods reported are off- HBLs for the constituents summarized constituent HBLs, and for the municipal site manufacturer refurbishing for reuse, below in Table III–14: landfill scenario we compared TCLP

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TABLE III±14.ÐCHARACTERIZATION OF FEED GAS FILTERS FROM INORGANIC HCN PRODUCTION [mg/kg or mg/L]

Constituent Total TCLP SPLP HBL

Boron ...... 17,900 7.4 <0.5 1.4 Lead ...... 18.5 1 0.03 1 0.003 0.015 Nickel ...... 91.0 0.4 <0.05 0.31 Zinc ...... 1,060 13 <0.5 5 1 Results are less than the typical laboratory reporting limit, but are greater than the calculated instrument detection limits.

Split sample results provided by the the environment. For a more complete management method reported was on- facility were comparable. We did not description of this analysis, see ‘‘Risk site Subtitle C disposal as a find cyanide in these wastes. Assessment for the Listing nonhazardous waste. The cartridge-type The full analytical results are Determinations for Inorganic Chemical filter elements are used in the process summarized in the ‘‘Inorganic Hydrogen Manufacturing Wastes’ in the docket. to prevent clogging of spray nozzles Cyanide Listing Background Document Thus, we propose not to list this waste used to inject the hydrogen cyanide for the Inorganic Chemicals Listing as hazardous. intermediate product into the HCN Determination’’ and are reported in stripper. The filters remove process detail in the Waste Characterization TABLE III±15.ÐGROUNDWATER RISK particulates, including rust, from the Reports for this sector; these documents RESULTS FOR FEED GAS FILTERS hydrogen cyanide intermediate product. are available in the docket for today’s FOR BORON The waste is generated when the spent proposal. filter elements are replaced weekly. While this waste is classified as How Was the Groundwater Ingestion Percentile Adult Child HQ HQ nonhazardous, the generator disposes of Risk Assessment Established? it in the facility’s on-site Subtitle C We assessed the groundwater 90th ...... 0.007 0.01 landfill. ingestion pathway for the off-site 95th ...... 0.01 0.05 landfill scenario for this waste, How Was This Waste Category reflecting the types of management (5) Process air cartridge filters. Characterized? reported. As noted in section III.E., we How Many Facilities Generate This No sample of this waste was collected used the TCLP results for the municipal Waste Category and How Is It Managed? because of unavailability during the landfill scenario and the SPLP for the Eight facilities reported a total volume sampling time frame and because the industrial landfill scenario. We found of 7.5 MT/year for this waste. The level of toxic constituents is expected to that the industrial Subtitle D landfill management methods reported are off- be low. The filters are used to remove scenario screened out because all site industrial D landfill, off-site inert impurities such as pipe scale. The constituents in the SPLP analysis were manufacturer refurbishing for reuse, off- facility washes the filters prior to below their respective HBLs. site municipal D landfill, and on-site removal of the filters from the process. The constituents of concern that industrial D landfill. Most facilities We expect that any hydrogen cyanide exceeded their respective HBLs in the reported the practice of filtering the air contamination is removed during this TCLP results were boron, lead, nickel, that they feed to the reactors. Very small washing. The facility reported in its and zinc. We evaluated these volumes of spent filters are generated RCRA Section 3007 Survey that the constituents using the de minimis periodically. We did not assess these waste contains a total concentration of volume screening analysis, as described wastes beyond the characterization cyanide of one ppm. in section III.E.3 of today’s proposal. provided in the RCRA Section 3007 The analysis suggests that lead, nickel What Is EPA’s Listing Rationale for This Survey results because no wastes were Waste? and zinc are not of concern. We available to sample when we conducted We propose not to list this waste as modeled the remaining constituent, our sampling. The level of toxic hazardous because the level of toxic boron, using our standard groundwater constituents is expected to be low model for the municipal landfill because the filters are only used to constituents found in this waste are scenario. We modeled the municipal remove airborne solids from the ambient expected to be below levels of concern. landfill scenario, using a hydrogeologic air used in the process. While we do not have any leaching test setting reflecting the region where the data, we can conservatively estimate waste was reported to be managed. What Is EPA’s Listing Rationale for This that any leachable level of cyanide Waste? would be at least 20-fold less than the What Is EPA’s Listing Rationale for This 1 ppm total level reported, i.e, less than Waste? We propose not to list this waste as hazardous because we do not believe 0.05 mg/L. This is well below the HBL As noted above, the industrial landfill that the level of any toxic constituents for amenable cyanide (0.3 mg/L). scenario screened out. For the in these small waste volumes would Furthermore, this small volume waste is municipal landfill scenario, the results exceed levels of concern that would already managed in a Subtitle C landfill. in Table III–15 show that the HQs are pose a risk based on management in (7) Spent catalyst. All ten facilities well below one at both the 90th and Subtitle D landfills. reported generation of this waste, with 95th% for the constituent of concern. (6) Acid spray cartridge filters. a combined total volume of 4.1 MT/ Thus, our risk assessment results year. The management method reported suggest that the only constituent of How Many Facilities Generate This was off-site metals reclamation or concern that required modeling (boron) Waste Category and How Is It Managed? regeneration. These catalysts gradually does not pose a substantial present or One facility reported a total volume of lose their effectiveness over time and potential hazard to human health and 1.1 MT/year for this waste. The are periodically reclaimed. Due to the

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We have chosen not to evaluate the ‘‘commingled wastewaters’’ (10) HCN polymer and HCN sump these materials further because category. wastes. One facility reported a total management practices for these volume of 0.7 MT/year (0.3 MT/yr What Management Scenarios Were polymer and 0.4 MT/year sump wastes) materials prior to reuse minimize the Assessed? potential for environmental releases. for these two wastes. The physical Therefore, we propose not to list this We did not assess these numerous description of the wastes was reported waste as hazardous because there are no wastewater streams individually. The as dirt, debris and inert polymer solids. significant known exposure pathways wastewaters were assessed indirectly The wastes are disposed of in an off-site that would present risk. within the commingled wastewater industrial Subtitle D landfill. Very small (8) Ammonium sulfate and category discussed earlier. The volume volumes of these wastes are generated ammonium phosphate. and constituents represented by these periodically. We did not assess these miscellaneous wastewaters are wastes beyond the characterization How Many Facilities Generate This represented in the total commingled provided in the RCRA Section 3007 Waste Category and How Is It Managed? major and miscellaneous wastewater Survey results because of the Three facilities reported a total streams. unavailability under the sample volume of 27,425 MT/year for this How Was This Waste Category schedule and because of the low waste. The management method Characterized? concentrations of toxic constituents reported was off-site use as fertilizer. expected to be present in this waste. We did not collect samples of these In the RCRA Section 3007 Survey, the What Management Scenarios Were miscellaneous wastewater streams. The one generator reported that total levels Assessed? levels of toxic contaminants in these of cyanide were 50 mg/kg for the HCN We assessed the agricultural end use wastewaters are reflected in the polymer and 5 mg/kg for the sump of this waste by comparing the total contaminant concentrations of the total wastes. These levels are unlikely to pose constituent results to the soil screening commingled wastewater streams at each a risk in a landfill scenario for these levels. In this case we evaluated the facility. See the commingled wastewater very small waste volumes. In support of material, because it is land applied. category discussed earlier in this section this, we note here, as we did above for for a discussion on how the commingled the acid spray filter cartridge waste How Was This Waste Category major and miscellaneous wastewater category, leaching test results would be Characterized? streams were characterized. Two of the at least 20-fold less than the total levels. One sample of this by-product was miscellaneous wastewaters were This would mean any leaching from collected from the Alabama site. The reported to contain potentially high sump waste would be below the HBL for analytical data results show that the concentrations of hydrogen cyanide cyanide. While this 20-fold factor would detected constituents of concern in the when generated. leave the HCN polymer somewhat above total analyses are below the soil What Is EPA’s Listing Rationale for This the HBL at 2.5 ppm cyanide, we note screening levels. In addition, we Waste Category? that groundwater modeling for cyanide compared the SPLP leaching results to for the ammonia recycle filters indicates the HBLs as a screen of potential We propose not to list this waste similar levels of cyanide in a larger groundwater exposure.39 The detected category as hazardous. There is no waste volume presents very low levels SPLP results are below the HBLs. The direct exposure pathway into the of risk in a landfill scenario. Therefore, analytical results showing the level of environment from these individual we propose not to list HCN polymer and toxic constituents are included in the wastes, because they are treated and HCN sump wastes. ‘‘Inorganic Hydrogen Cyanide Listing commingled with the other wastewaters (11) Sludge from wastewater Background Document for the Inorganic generated at each facility. Although high collection tank. One facility reported a Chemicals Listing Determination.’’ concentrations of hydrogen cyanide in volume of 2.1 MT over a seven year the wastewaters are possible for some of period, or approximately 0.3 MT/year What Is EPA’s Listing Rationale for This these wastes, the risk is reduced by the for this waste. The waste was coded as Waste? high dilution that occurs when these hazardous (D001), stabilized on-site and We propose not to list this waste as wastewaters are mixed with other large disposed of in an off-site Subtitle C hazardous because the levels of toxic volume wastewaters in the facility-wide landfill. The waste is generated constituents found in the waste are wastewater collection system. These approximately every ten years; the below levels of concern. miscellaneous wastewaters are volume reported was for 1993 with no (9) Miscellaneous wastewaters. generated intermittently and generation of that waste since that date. infrequently. Thus, any potential This waste results from sedimentation How Many Facilities Generate This releases from land-based management of in a wastewater collection tank. HCN Waste Category and How Is It Managed? the wastes after dilution in with other wastewaters managed in this tank only Four facilities reported a total volume wastewaters would be short-lived, and account for ten percent of throughput; of 209,000 MT/year for this waste unlikely to result in any significant the sediment thus is only marginally long-term risk. In addition, the associated with HCN production. One 39 Note that the SPLP/HBL groundwater screen for hydrogen cyanide contaminant is other facility reported generating 1.8 MT this scenario is likely to be a worse-case screening, because the fertilizer application scenario isn ot readily and rapidly treated in the of this waste, and also codes it as analogous to a landfill scenario, particularly with wastewater treatment systems, so that characteristically hazardous waste (in respect to application rates. any risk is minimized. For example, the this case as D018 for benzene). This

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00041 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55724 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules second facility sends the waste off-site reported concentrations of cyanide (1 is generated approximately every ten to a Subtitle C incinerator; the facility mg/kg) and ammonium sulfate (5,000 years; the volume reported was for 1993 reported that the benzene was derived mg/kg). This concentration of cyanide is with no generation of the waste since from other on-site processes. We considered to be very small and is not that date. Thus, on an annualized basis propose not to list these wastes because expected to be of concern (see the waste quantity generated would be they are very small volume wastes that discussion of cyanide for acid spray approximately 4 MT/yr. We did not are already managed as cartridge filters). In addition, we assess these wastes beyond the characteristically hazardous wastes in collected a sample of the ammonium characterization provided in the RCRA full compliance with the Subtitle C sulfate by-product (i.e., the material Section 3007 Survey results because of regulations. In addition, the wastes are being filtered to generate this waste) and the unavailability of samples under the generated from the treatment of did not find any constituents of sample schedule. We propose not to list predominantly non-HCN wastewater concern. See discussions for ammonium this waste as hazardous because the from unrelated petrochemical processes sulfate and ammonium phosphate. waste is managed as characteristically at the facilities. Therefore, we propose not to list this hazardous in accordance with all (12) HCN storage tank solids. One waste as hazardous because we do not applicable Subtitle C standards, which facility reported a volume of 0.3 MT/ believe that there are any significant adequately protect against year for this waste. During periodic levels of toxic constituents in the waste. mismanagement. Further, the waste is shutdowns of this product tank for (15) Spent ammonium phosphate. generated from the treatment of cleaning, solids are removed after One facility reported a volume of 230 predominantly non-HCN wastewater rigorous washing of the tank interior to MT/year for this waste. The waste is from other unrelated petrochemical remove soluble cyanide. The waste reused on-site as a nutrient source in the processes at the facility. Only ten consists of polymer and tank scale. The biological treatment unit or incinerated percent of the wastewater throughput in waste is disposed of in an off-site on-site in a nonhazardous waste the tank generating this waste is municipal Subtitle D landfill. A sample incinerator. The waste is generated in associated with HCN production; the of this waste was not collected because batches one or two times per year. The percentage contribution from the HCN of unavailability during the sampling waste is generated from the scrubbing of process to this oily layer is likely to be time frame. However, the waste the reactor off-gas stream using aqueous much lower, because other description provided by the facility monoammonium phosphate solution in petrochemical processes on-site are indicates the waste is similar in the ammonia recovery process. The likely sources of the organic material. composition to the ammonia recycle resulting diammonium phosphate filters, which we have proposed not to solution is then purified to recover the 6. Phenyl Mercuric Acetate list. Given the much smaller volume ammonia and the resulting spent a. Summary. We propose not to list here, this waste is not expected to ammonium phosphate solution is stored any wastes from the production of present significant risk. Therefore, we in tanks prior to final management. We phenyl mercuric acetate (PMA) as are proposing not to list this waste as did not assess this waste beyond the hazardous under Subtitle C of RCRA. hazardous. characterization provided in the § 3007 PMA currently is not manufactured in (13) Wastewater filters. One facility Survey results because of the the United States, and it is extremely reported a volume of 450 MT/year for unavailability of samples under the unlikely that it will be manufactured in this waste. The waste is managed in a sample schedule; the characterization the United States in the future. captive, off-site Subtitle C incinerator as indicates the presence of organonitrile Therefore, there are no wastes being characteristically hazardous waste. The compounds in the waste. However, the generated that could be subject to a waste is spent filters from the filtration preferred management method is to listing determination. of commingled wastewaters from reuse the waste as a nutrient source in b. Description of the phenyl mercuric various on-site processes prior to on-site the biotreatment system, with acetate industry. PMA (C8H8Hg O2) is an deepwell injection and is generated incineration only when this is not organic mercury compound, a white to periodically. A sample of this waste was possible due to the solution becoming creamy white odorless crystalline not available during the sampling time spent or when the concentrations of powder or clear solution. Prior to 1990 frame. However, the one generator phosphate and ammonia are it was the predominant fungicide used reported that the waste is incompatible with the wastewater in the latex paint industry. In 1990, EPA characteristically hazardous due to treatment system. We believe the levels banned the use of PMA in interior paint benzene, and the facility manages the of organonitrile compounds do not pose (55 FR 26754, June 29, 1990) and waste as D018. The source of the a risk under either management subsequently, the paint industry ceased benzene is the waste from other non- scenario. The wastewater treatment using PMA in paint production. PMA is HCN process wastewaters at the facility. scenario results in the destruction of the still used for other limited purposes We propose not to list this waste compounds via biodegradation and the (e.g., slimicide in paper mills; selective because it is already managed as a incineration scenario would also result herbicide for crabgrass; fungicide for hazardous waste in accordance with in destruction of the volatile diseases of turf on golf greens and tees; Subtitle C regulations. organonitriles. Additionally, emissions fungicidal seed dressing for seed- and (14) Ammonium sulfate filters. One from the on-site incinerator would be soil-borne diseases of cereals, sorghum, facility reported a volume of 1.1 MT/ regulated under the Hydrogen Cyanide and groundnuts). year for this waste. The waste is MACT standards which will be Based on our research and the results managed in an off-site industrial proposed in 2000. Therefore, we of our RCRA Section 3007 Survey, we landfill. The waste is generated propose not to list this waste as conclude that there is no domestic periodically. We did not assess this hazardous. production of PMA. Any domestic waste beyond the characterization (16) Organic layer from wastewater demand is met by imports from other provided in the RCRA Section 3007 collection tank. One facility reported a countries. See the ‘‘Phenyl Mercuric Survey results because of the volume of 43.3 MT/year for this waste. Acetate Listing Background Document unavailability of samples under the The waste is coded as D001 and sent off- for the Inorganic Chemical Listing sample schedule. However, the facility site Subtitle C incineration. This waste Determination’’ for details.

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c. Agency evaluation. PMA is not identified fourteen waste categories —Spent filters for product are generated produced within the United States and from the production of phosphoric acid when product is filtered prior to is not widely used in domestic (via the dry process) that required loading into tank cars and trucks to manufacturing processes. Therefore, we assessment. These waste categories are remove settled solids. The filters are have no reason to believe that wastes described briefly and in more detail in changed periodically and rinsed with from the production of PMA are the following subsections.40 water prior to disposal. generated within the U.S. Given the —Arsenic filter cake is the result of —Spent activated carbon for off- compound’s limited market within the filtering the phosphoric acid after the specification product is generated U.S., it is highly unlikely that new addition of sodium hydrosulfide or when carbon is used to remove traces production of PMA will occur within hydrogen sulfide gas and a filter aid. of contaminants from the off- the U.S. in the future. As a result of The precipitate consists of arsenic specification product. these market conditions, there are no trisulfide and other heavy metal —Spent filters for off-specification wastes that can be assessed for this sulfides which are essentially product is generated when filters are sector. Therefore, we propose not to list insoluble in strong acid. used to remove solids from the off- any PMA production wastes as —Combustion chamber slag specification product. hazardous. (infrequently generated) is the result —Wastewater treatment sludges are 7. Phosphoric Acid From the Dry of residue buildup on the walls of the generated when wastewaters from the Process chamber. phosphoric acid and other processes —Off-specification phosphoric acid is are treated. These sludges are only a. Summary. We have evaluated the generated when the product does not marginally derived from phosphoric wastes from the production of meet color or concentration acid wastewaters due to commingling phosphoric acid manufactured via the specifications. with large volumes of other non- dry process, and propose not to list any —Spent filters (from purification) are phosphoric acid wastewaters. The wastes from this process as hazardous generated from the units that are used solids that are removed by filtration wastes. These wastestreams do not meet to remove arsenic from the are landfilled or sold. the criteria set out at 40 CFR phosphoric acid. 261.11(a)(3) for listing wastes as Three facilities reported that they —Caustic scrubber water is generated hazardous. They do not pose a collect phosphoric acid in air pollution when air used to remove hydrogen substantial present or potential threat to control devices (i.e., vent scrubbers, human health or the environment. We sulfide gas at the acid purification absorbers, mist eliminator). Each site have identified no risks of concern step is scrubbed. This scrubbing reported that they then recycle these associated with the current management operation controls odor and acid mist acids into the production process. This of these wastes. before the air is discharged to the material is continuously reused in the b. Description of the phosphoric acid atmosphere. production process. Based on our site industry. —Phosphoric acid spills occur around visits, the material is piped from the Phosphoric acid was produced by the the process or storage tanks area. generating unit to the production dry process by eight facilities in the These materials are collected in process, minimizing the potential for United States in 1998. The majority of contained areas and pumped to releases to the environment prior to phosphoric acid is consumed in the management units. reuse. We evaluated all wastes manufacture of phosphate salts. These —Clean-up and washdown water from generated after the materials are reused phosphorus-containing compounds are across the units is collected in a sump and concluded that none merited used in detergents, animal feed and discharged to the wastewater listing. Consequently, we do not believe supplements, dentifrices, fertilizers, treatment system. that these materials present significant metal treating, water softening, —Process acid leaks occur when piping threats. leavening agents, and flame and fire and coupling break, or during At two of the facilities, the caustic retardants. equipment maintenance. These scrubber water, generated from In the dry process, elemental materials are collected in contained scrubbing the air to remove hydrogen phosphorous is burned in excess air areas and pumped to management sulfide gas, is returned as makeup generating phosphorous pentoxide units. solution to the purification process. (P2O5). The resulting phosphorus —Spent mist eliminator packing (filters) Based on information from one of the pentoxide is hydrated with a spray of are used in the scrubber system to facilities and our site visit, the material recycled phosphoric acid and water, remove gas and acid particulates from is piped from the generating unit to the forming phosphoric acid that is the phosphoric acid. The filter production process, and there is no collected as product. Scrubbers are packing material is reported to consist significant potential for exposure. Also, employed for the hydrator off-gases to of polyester fibers, stainless steel, process acid leaks are collected in tanks absorb as much phosphoric acid mist as steel wool or fiberglass. The filters are at one facility and piped back to the possible from the excess air. The strong periodically replaced and the spent acid process, with no significant phosphoric acid stream from the packing is washed prior to disposal. exposure route for this material. As hydrator is purified with hydrogen —Rubber liners of product storage tanks stated above, we evaluated all wastes sulfide to precipitate out arsenic are periodically replaced. generated after the materials are reused trisulfide. This sludge is removed by and concluded that none merited filtration. In some cases, off- 40 One facility has shut down their phosphoric listing. Consequently, we do not believe acid process and reported few wastes generated in specification product is filtered and 1998. This facility’s wastes therefore are not that these materials present significant recycled into the process. The product included in the following overview, but were threats. may also be filtered after it leaves the evaluated to determine their potential threat to We have organized our discussion of storage tank and prior to loading in human health or the environment. The details of these wastes in terms of how they are this facility’s waste generation and management truck and railcars. practices are included in the ‘‘Phosphoric Acid currently managed: characteristic c. Description of wastes generated by Listing Background Document for the Inorganic wastes, wastewaters, and non- the phosphoric acid process. We have Chemical Listing Determination’’. characteristic solid wastes.

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d. Agency evaluation. (1) they exhibit the characteristics of prior to land disposal. Furthermore, Characteristic wastes. The RCRA corrosivity or toxicity for arsenic. We these wastes are managed or disposed in Section 3007 Surveys show that a believe that these wastes are managed Subtitle C management units. Table III– number of wastes are managed as RCRA according to the applicable RCRA 16 summarizes our information characteristic wastes at all times. These Subtitle C regulations, including LDR regarding the generation and wastes are hazardous wastes because standards. The LDR restrictions apply management of these wastes.

TABLE III±16.ÐCHARACTERISTIC WASTES FROM PHOSPHORIC ACID PRODUCTION DISPOSED IN SUBTITLE C UNITS

Number of Waste category reported 1998 Volume Reported hazard codes Final management practices generators (MT)

Arsenic filter cake ...... 7 614 D002, D004 ...... Subtitle C landfill Combustion chamber slag ...... 1 0.1 D002 ...... Subtitle C incineration Off-specification phosphoric acid ... 1 0.71 D002 ...... Subtitle C landfill Spent filters (from purification) ...... 2 4.6 D004 ...... Subtitle C incineration or Subtitle C landfill

We propose not to list these four materials as hazardous from the point of believe that the rules applying to waste categories as hazardous wastes generation through disposal, because characteristic wastes adequately protect under RCRA. All generators of these they exhibit one or more of the against mismanagement. wastes already report managing these hazardous waste characteristics. We (2) Other characteristic waste.

TABLE III±17.ÐOTHER CHARACTERISTIC WASTES FROM THE PRODUCTION OF PHOSPHORIC ACID

Number of Waste category reported 1998 Volume Reported hazard codes Sequential management practices generators (MT)

Phosphoric acid spills ...... 2 2.2 D002 ...... (1) Neutralized, (2) roll-off bin, (3) Subtitle D landfill; (1) Tanks, (2) neutralized in sur- face impoundment, (3) NPDES

We assessed the specific management tanks because we assume that they (3) Wastewaters. Wastewaters are practices employed for this function effectively. With regard to the generated at various points in the wastestream, as summarized in Table surface impoundment, we note that the process as a result of scrubbing III–17, and determined that no exposure facility has estimated that these small operations, equipment cleanup, and scenarios of concern exist. One facility volume spills make up less than 0.001% management of leaks and spills. As reported that the wastestream is of the total wastewater volumes. We reported by the facilities, the primary managed as hazardous (D002), expect that dilution of this magnitude constituents of concern in these neutralized, and disposed of in a would effectively treat the spills wastewaters are phosphoric acid and Subtitle D landfill. These product spills rapidly. Further, the facility reported traces of hydrogen sulfide, which are are expected to be mostly phosphoric that the wastewaters in the readily treated and controlled via acid, which is hazardous because it is impoundment are neutralized. neutralization. Phosphoric acid, when corrosive. The facility effectively treats Consequently, we do not anticipate that neutralized, forms various phosphate and neutralizes these wastes prior to any potential releases from the surface disposal. There is no significant risk impoundment would pose a significant salts, none of which are known to pose expected from the disposal of the small threat to groundwater. Ultimately, the a significant risk to human health and volume (0.5 MT/yr) of treated spills to spills are discharged, along with the the environment. Similarly, hydrogen the landfill. much larger volume of wastewaters sulfide is neutralized to form The second facility reported placing generated on-site, to surface waters nonvolatile salts. All facilities report the untreated spills into its wastewater under a NPDES permit, which provides that these wastewaters comprise very treatment system, which includes both effective control and an exemption from small portions of the overall wastewater tanks and impoundments. Again, we RCRA regulations. We also note that we treatment throughput, which contains expect that this waste presents hazards expect no release of constituents of wastewaters from other unrelated on- because of its corrosivity, not because it concern to the air from either the tank site processes. Table III–18 summarizes contains hazardous constituents. We do or the impoundments, because the our information on these wastewaters. not expect releases to groundwater from waste contains no volatile constituents.

TABLE III±18.ÐWASTEWATERS FROM PHOSPHORIC ACID PRODUCTION

Number of Waste category reported 1998 Volume Reported hazard Sequential management practices generators (MT) codes

Caustic scrubber water ...... 1 36 none ...... (1) pretreatment in covered tanks, (2) POTW

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TABLE III±18.ÐWASTEWATERS FROM PHOSPHORIC ACID PRODUCTIONÐContinued

Number of Waste category reported 1998 Volume Reported hazard Sequential management practices generators (MT) codes

Cleanup water ...... 1 small volume none ...... (1) pretreatment in covered tanks, (volume not (2) POTW reported) Process acid leaks ...... 1 251 none ...... (1) pretreatment in covered tanks, (2) NPDES 1 The 25 tons include leaks from eight processes, of which one is phosphoric acid production. The individual volume of leaks from phosphoric acid production is unknown.

We have assessed the management wastewater releases. Thus, based on the designed to neutralize this compound, practices employed for these wastes and lack of any significant likelihood of reducing the potential for volatilization. determined that no exposure pathway of release of the constituents to In addition, the facilities have installed concern exists. We believe these groundwater, we did not project tank covers, further reducing the wastewaters will continue to be significant risks to groundwater from likelihood of release to the air. As a managed in existing tank-based these wastes in the tank-based result, we did not model releases to air treatment systems. We believe the wastewater treatment scenario. from tanks from the production of manufacturers have made a Furthermore, discharges to POTWs and phosphoric acid. Thus, we propose not considerable investment in wastewater surface waters under NPDES are to list these wastewaters as hazardous treatment systems using tanks and will regulated under the Clean Water Act wastes under RCRA. continue to use them. Further, we and are exempt from RCRA Subtitle C (4) Non-characteristic solid wastes. assumed that wastewater treatment regulation and thus were not assessed. The phosphoric acid sector reported six tanks retain sufficient structural We also considered the possibility of waste categories that do not routinely integrity to prevent wastewater releases air releases from tanks. The only exhibit any of the hazardous waste to the subsurface (and therefore to potential volatile constituent of concern characteristics and that are often groundwater), and that overflow and in these wastes is hydrogen sulfide. The managed in Subtitle D landfills, as spill controls prevent significant treatment processes employed are summarized in Table III–19:

TABLE III±19.ÐNON-CHARACTERISTIC SOLID WASTES

Number of Waste category reported 1998 Volume Reported hazard Sequential management generators (MT) codes practices

Spent mist eliminator packing ...... 5 28.4 None ...... (1) storage in containers, (2) treatment to control acid (washing, neutralization, or off-site stabilization by one facility), (3) re- cycling or disposal in Subtitle C or D land- fills. Rubber liners ...... 2 19.8 None ...... (1) storage in containers, (2) Subtitle C in- cineration or neutralization before Subtitle D landfill. Spent filters for product ...... 1 0.5 None ...... (1) storage in containers, (2) off-site sta- bilization, (3) Subtitle D landfill. Spent activated carbon for off-specification 1 1 3 None ...... (1) storage in containers, (2) off-site sta- product. bilization, (3) Subtitle D landfill. Spent filters for off-specification product ...... 1 0.5 None ...... (1) storage in containers, (2) off-site sta- bilization, (3) Subtitle D landfill. Wastewater treatment sludges ...... 3 2 0.005 None ...... (1) storage in containers, (2) Subtitle D landfill. 1 1996 volume; none generated in 1997 or 1998. 2 Two facilities did not report volumes due to very small input of phosphoric acid production wastes to the WWT system; one facility estimated that 0.0001% of 4,640 MT sludge generated (or 0.005 MT) was from phosphoric acid production.

The spent mist filters collect constituents. Thus, arsenic is not it is unlikely that they contain any phosphoric acid mist before arsenic expected to adhere to the filters as constituent at levels of concern (i.e., trisulfide is precipitated out. The condensate drops back into process. The above health-based limits for ingestion). material which condenses in the filters generators treat the spent filters prior to We also note that both wastes are is expected to be corrosive and may disposal to remove or immobilize any treated prior to disposal in landfills. contain some arsenic. However, the low levels of constituents that may Similarly, we do not expect the spent material used for filter packing in the remain. carbon or spent filters associated with mist eliminators is typically polyester, The rubber liners and spent filters for off-specification product to contain fiberglass, or steel wool. The filter product are associated with food-grade significant levels of constituents of packing provides surface area for products. We expect any contaminant concern. Product is classified as ‘‘off- condensation, not absorption, and is not levels to be extremely low due to purity specification’’ due to color and expected to accumulate waste or requirements. Consequently, we believe concentration of acid, rather than

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00045 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55728 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules because of the presence of any phosphorus pentasulfide vapors are —Scrubber water is generated as a result contaminants. We note again that these distilled and the liquid from the process of a nitrogen stream being scrubbed to wastes undergo treatment prior to is solidified, milled and packaged. remove phosphorus pentasulfide dust. placement in landfills. In addition, both One facility operates its entire process The packaging equipment is filled the activated carbon, which is under nitrogen blanket. The blanketed with nitrogen to prevent oxidation. infrequently generated, and the off- vessels, packaging area and tote-bin —Caustic scrubber water is the result of specification filters are very low volume wash systems are all vented to a caustic the reactor, packing and tote bin wash wastes (on an annualized basis, the scrubber. A second facility vents the system being vented to the scrubber to spent carbon totals about 1 MT and the reactor to a caustic scrubber that remove sulfur dioxide and residual spent off-specification filters equal 0.5 removes the sulfur dioxide and hydrogen sulfide. MT). hydrogen sulfide and generates a —Tote bin wash water results from As stated in the wastewater rationale, blowdown wastestream. The facility has cleaning the shipping containers that the wastewater contribution from the other scrubbers that remove phosphorus phosphoric acid process is insignificant. hold the product. The phosphorus pentoxide from the exhaust stream and pentasulfide residue is washed from Therefore, the volumes of treatment reacts it with water to produce a dilute sludge (and any constituents of the returned containers with water phosphoric acid that is routed to their and caustic. potential concern) attributable to the acid plant. The third facility fills the phosphoric acid process are small and reactor, condenser and packaging — sulfur is occasionally generated unlikely to present any significant risk. equipment with nitrogen to prevent when making or breaking couplings to We do not believe any of these oxidation. This nitrogen stream is hoses where sulfur comes into the materials contain significant scrubbed with recirculating water to reaction. concentrations of any contaminants of remove phosphorus pentasulfide dust. One facility reported that they filter concern. Therefore, we propose not to The scrubber liquor is treated and elemental phosphorus before feeding it list these wastes as listed hazardous discharged. to the reactor. The filter solids, called wastes under RCRA. c. Description of wastes generated by phosphorus impurities, are managed in 8. Phosphorus Pentasulfide the phosphorus pentasulfide process. tanks and then are piped to that We have identified nine waste facility’s phosphoric acid production a. Summary. We have evaluated the categories from the production of furnace for phosphorus reclamation. wastes from the production of phosphorus pentasulfide that required Because there is low potential for phosphorus pentasulfide and propose assessment. These waste categories are significant exposure from on-site storage not to list any wastes from this process described briefly and in more detail in prior to entry in the furnace, we did not as hazardous. These wastestreams do the following subsections. evaluate this material further under this not meet the criteria set out at 40 CFR sector. Note that wastes generated from 261.11(a)(3) for listing a waste as —Still residue/reactor waste is the the production of phosphoric acid via hazardous. They do not pose a result of impurities being left behind the dry process, including this facility’s substantial present or potential threat to when the phosphorus pentasulfide is phosphoric acid furnace, are addressed human health or the environment. We distilled to remove undesirables (high in section III.F.7 of today’s proposal. have identified no risks of concern boilers). This residue consists of associated with the current management glassy phosphates, carbon, and iron We have organized our discussion of of these wastes. sulfide compounds and is removed these wastes in terms of how they are b. Description of the phosphorus from the reactor during unit turn- currently managed: characteristic pentasulfide industry. Phosphorus around. wastes, wastewaters, and scrap sulfur. pentasulfide was produced by three —Phosphorus pentasulfide scrap waste d. Agency evaluation. (1) facilities in the United States in 1998. is occasionally generated during Characteristic wastes. The RCRA Phosphorus pentasulfide is used in the certain maintenance operations or Section 3007 Surveys show that a manufacture of lubricating oil additives, equipment failure. This waste can number of the phosphorus pentasulfide insecticides, ore flotation agents and also consist of commercial off- wastes categories are managed as RCRA specialty chemicals. specification material and fugitive hazardous wastes at all times. These The production of phosphorus dust from the packaging operation. wastes are hazardous because they pentasulfide begins by feeding liquid —Absorbents contaminated with exhibit the characteristics of ignitability, phosphorus and liquid sulfur into a phosphorus pentasulfide and reactivity or toxicity for chromium or reactor. The reaction is carefully Therminol (benzylated ethyl benzene) benzene. The facility that generates the controlled because phosphorus are generated from cleaning up leaks largest volume waste, phosphorus pentasulfide reacts violently with air during maintenance operations. The pentasulfide scrap waste, considers it to forming phosphorus pentoxide and absorbent material may be in the form be a listed hazardous waste (U189). The sulfur dioxide and because toxic of floor dry (a granular material) or an surveys also show that these wastes are hydrogen sulfide gas forms when absorbent pillow. managed as hazardous wastes, with phosphorus pentasulfide combines with —Waste Therminol is a spent heat final disposition by incinerated in moisture on exposure to air. To reduce transfer product used for the vessels Subtitle C units. Table III–20 this hazard, the process equipment is and pipes to prevent freeze up of the summarizes our information about these continuously purged with nitrogen. The liquid phosphorus pentasulfide. wastes.

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TABLE III±20.ÐCHARACTERISTIC WASTES FROM PHOSPHORUS PENTASULFIDE PRODUCTION DISPOSED IN SUBTITLE C UNITS

Number of Waste category reported 1998 volume Reported hazard Final management practices generators (MT) codes

Still residue/reactor waste ...... 2 4.6 D003, D007 ...... Subtitle C incineration. Phosphorus pentasulfide scrap waste ...... 3 67.75 D001, D003, Subtitle C incineration. U189. Contaminated absorbent ...... 1 1.2 (1996) D003 ...... Subtitle C incineration. Waste Therminol ...... 1 1.4 D018 ...... Subtitle C incineration.

We propose not to list these four percent of the waste are already listed hydrogen sulfide which are readily waste categories as hazardous wastes as commercial chemical product (U189). controlled via neutralization. The under RCRA. All generators of these Therefore, we propose not to list these management practices for these wastes already report managing these wastes. wastewaters do not allow for the release materials as hazardous from the point of (2) Wastewaters. Wastewaters are of phosphoric acid and hydrogen sulfide generation through incineration because generated at various points in the to the environment in an undiluted or they exhibited one or more of the process as a result of scrubbing unneutralized state. Table III–21 hazardous waste characteristics. Again, operations and tote bin washing. As summarizes our information on these the rules applying to characteristic identified by the facilities, the primary wastewaters: wastes adequately protect against constituents of concern in these mismanagement. Furthermore, ninety wastewaters are phosphoric acid and

TABLE III±21.ÐWASTEWATERS FROM PHOSPHORUS PENTASULFIDE PRODUCTION

Number of Waste category reported 1998 Volume Reported hazard Sequential management practices generators (MT) codes

Process scrubber water ...... 1 77,377 none ...... (1) Sewer, (2) POTW Caustic scrubber water ...... 2 2,177 none ...... (1) Covered tanks, (2) off-site treatment, (3) NPDES; (1) Treatment in covered tanks, (2) POTW. Tote bin wash water ...... 2 188 (1) D003 ...... (1) Covered tanks, (2) none ...... (2) off-site treatment, (3) NPDES; (1) Treatment in covered tanks, (2) POTW.

We assessed the management periodically exhibit a characteristic, the b. Description of the phosphorus practices for these wastes and generator always manages the waste in trichloride industry. Six facilities in the determined that no exposure pathway of a Subtitle C incinerator. We believe this United States reported producing concern exists. Thus, we propose not to management practice is likely to phosphorus trichloride in 1997 or 1998. list these wastes as listed hazardous continue because the cost to treat it as We are assessing wastes from the five wastes under RCRA. The covered tanks hazardous is low for such a small facilities that still produce this employed minimize potential for volume wastes, and because the waste product.41 releases to groundwater and air. may be TC hazardous as generated. This Phosphorus trichloride is used as an Discharges to surface waters under waste is also small volume and highly intermediate in the production of a NPDES are exempt from RCRA unlikely to present a significant risk. variety of chemicals. These chemicals regulation. Discharges to POTWs via the are used to make pesticides, herbicides, 9. Phosphorus Trichloride facility’s common sewage line are antiscaling additives, corrosion excluded from RCRA (40 CFR a. Summary. We have evaluated the inhibitors for cooling towers and heat 261.4(a)(1)(ii)). wastes from the production of exchangers, surfactants, sequestrants, (3) Scrap sulfur. One facility reported phosphorus trichloride and propose not and textile-treating agents. Phosphorus generation of scrap sulfur that to list any wastes from this process as occasionally exhibits the characteristic hazardous wastes. These wastes do not 41 One facility discontinued production as of of TC for lead. This sulfur is managed meet the criteria set out at 40 CFR November 1999 and has no future plans to resume production of phosphorus trichloride. This facility’s as hazardous in a Subtitle C incinerator. 261.11(a)(3) for listing a waste as wastes therefore are not included in the following The 1998 waste volume was 0.12 MT. hazardous. They do not pose a overview, but were evaluated to determine their We do not believe this material substantial present or potential threat to potential threat to human health or the warrants listing as hazardous waste and, human health or the environment. We environment. The details of this facility’s waste generation and management practices are included therefore, propose not to list this waste have identified no risks of concern in the ‘‘Phosphoric Acid Listing Background as hazardous under RCRA. While this associated with the current management Document for the Inorganic Chemical Listing waste category was reported to of these wastes. Determination.’’

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00047 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55730 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules trichloride is used as a raw material in sludge removal step. These materials One facility reported recycling three the production of chemicals that are are treated and discharged to an secondary materials: phosphorous used extensively as lubricating oil POTW and under a NPDES permit. storage tank sediment; phosphorous additives to control corrosion and as —Product storage tank cleanout with transfer water; and absorber residual. antioxidants and flame retardants in nonreactive phosphate ester is the The phosphorous storage tank sediment plastics. rinsate generated from cleaning the is generated periodically when the Phosphorus trichloride (PCl3) is a storage tank or equipment. When this phosphorus storage tanks are cleaned. clear, volatile liquid with a pungent, rinse is done, the rinsate is drummed Because the material is stored in irritating odor. Phosphorus trichloride is for off-site disposal as a hazardous containers prior to being sent off-site for produced by one basic process. Liquid waste. recovery of phosphorus we found low phosphorus and chlorine gas are —Product storage tank cleanout with potential for significant exposure from continuously introduced into a reaction water is generated as a result of on-site storage. The phosphorous vessel. The phosphorus trichloride additional rinsing that follows recovery process is outside the scope of vapor phase is purified in a packed phosphate ester rinsing. This the consent decree so we did not column and then liquified in a potentially acidic rinse water is sent evaluate its wastes. At this same facility, condenser. Most raw material impurities to wastewater treatment for raw material phosphorous is unloaded remain in the reactor and are removed neutralization. from rail cars and conveyed through the as solid waste periodically during unit —Spent filter washwater for product is facility using a closed pressurized turnaround. Some facilities filter the generated as the result of washing the piping system that uses water to push product before shipment to ensure there spent filters used to remove dirt and the phosphorous in the piping system. is no dirt or other particles in the final particles from the product. This wash To unload the phosphorous from each product. water is mixed with other rail car, water is pumped into the rail A scrubber is used to collect materials wastewaters and sent to wastewater car to push the phosphorous out. from various points in the process. For pretreatment. Because the phosphorous/water filled example, hydrochloric acid and —Process area wash water consists of rail cars are then returned to the phosphorous manufacturers, where the phosphorus acid (H3PO3), the hydrolysis pad washdown/rain water and any products of phosphorus trichloride spilled material collected in phosphorous is then recovered, we vapors are vented to the scrubber from contained areas. This wash water is found no potential for significant the reactor. Also, phosphorus mixed with other wastewaters and exposure, and did not evaluate this trichloride vapor generated during sent to wastewater pretreatment. material further. The third instance of transfer of the product into shipping —Final washout water from reactor is recycling at this facility, gases vented containers is collected and vented to the the rinsate from additional reactor from the product check, storage tanks, same scrubber. The wastewater washing after sludge removal. The and reflux separator are collected in an absorber. The vapors from the absorber generated from the scrubber(s) is one facility reporting this rinsate are captured in a caustic scrubber and commingled with miscellaneous commingles it with other wastewaters sent to wastewater treatment (see wastewaters (e.g., reactor washout, prior to wastewater pretreatment. wastewaters in section d(2) below). spent filter wash, process area wash —Caustic scrubber water consists of According to the facility, the non-vapor water) and sent for treatment. Some small amounts of sodium salts and phosphorous trichloride residual from facilities generate a wastewater residual caustic. Phosphorus the absorber is collected and piped to a treatment sludge from the cleanout of trichloride, acid vapors, traces of treatment tanks. All of these facilities non-consent decree production process chlorine and carbon dioxide are where the phosphorous trichloride is produce a variety of other products that vented from various points of the are outside the scope of today’s rule, incorporated into the non-consent process. The vent releases mixed with decree product. Because this material is and they commingle the wastewaters air are scrubbed before the air is from PCl production with wastewaters piped from the phosphorous trichloride 3 released to the atmosphere. The spent process to the non-consent decree from other processes. scrubber charge is sent along with process, and there is no significant c. What kinds of wastes are generated other wastewaters to wastewater potential for exposure, we did not by this process?. We have organized our pretreatment. evaluate this residual further. discussion of these wastes in terms of —Process scrubber water consists of a d. Agency evaluation. We have how they are currently managed: weak acidic solution from scrubbing organized our discussion of these wastes characteristic wastes, wastewaters, residual gases from distillation and in terms of how they are currently recycled phosphorus, and non- from various storage tank vents. managed: characteristic wastes, non- characteristic non-wastewaters. The —Spent filters for product are generated characteristic wastewaters, and non- wastes generated by this process due to filtering dirt and other particles characteristic solid wastes. include: from the product before shipment. (1) Wastes that are characteristically —Reactor cleanout sludge consists of The filters are washed and dried hazardous wastes. Many of the impurities from the elemental before disposal. phosphorus trichloride producers stated phosphorus and chlorine raw —Wastewater treatment sludges are that a number of their wastes exhibit materials, including high boiling generated when wastewaters from the RCRA characteristics. These wastes are impurities such as arsenic trichloride phosphorus trichloride and other hazardous wastes because they exhibit that are retained in the reactor. These processes are biologically treated. the characteristics of ignitability, materials are sent to Subtitle C These sludges are only marginally corrosivity, reactivity or toxicity. The incinerators. derived from phosphorus trichloride Toxicity Characteristic was reported for —Initial washout water from reactor is wastewaters due to commingling with arsenic, cadmium, chromium, lead, generated as a result of rinsing out the large volumes of other non- mercury, selenium or silver. reactor after sludge removal. In one phosphorus trichloride wastewaters. These characteristic wastes are subject case, the reactor is cleaned with hot The solids that are removed by to the applicable LDR standards. water only and there is no initial filtration are landfilled. Furthermore, these wastes are

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TABLE III±22.ÐCHARACTERISTIC WASTES FROM PHOSPHORUS TRICHLORIDE PRODUCTION

Number of Waste category reported 1998 Volume Reported hazard Sequential management practices generators (MT) codes

Reactor cleanout sludge ...... 4 1 66 D001±004, (1) container D006±009, (2) Subtitle C incineration D010, D011. Initial washout water from reactor ...... 4 1 478 (1) D002, D004, (1) off-site pretreatment, D006, D007. (2) POTW; (2) D002, D004 (1) neutralized in tanks, (3) D004, D007 (2) surface impoundment, (3) biotreat in tank, (4) NPDES; (1) tank, (2) off-site biotreatment, (3) NPDES Product storage tank cleanout with nonreac- 1 10 D002, D003 ...... (1) container tive phosphate ester. (2) Subtitle C incineration Product storage tank cleanout with water ..... 1 15 D002 ...... (1) neutralized in tanks, (2) NPDES Spent filter wash for product ...... 1 15 D002 ...... (1) pretreatment in tanks, (2) NPDES Process area wash water ...... 1 1,400 D002 ...... (1) tanks, (2) NPDES 1 Volumes from 1996 or 1997 are included in the totals when the wastes were not generated by a facility in 1998.

For all but one of the wastes in the treated waste that enters the (2) Non-characteristic wastewaters. above table, the generators report impoundment, we do not believe this Wastewaters are generated at various managing these materials as hazardous waste is likely to pose significant risk. points in the process as a result of from the point of generation through The waste is generated infrequently scrubbing operations, equipment disposal (or the point at which they (once a year) and combined with cleanup, and washing the process area. become discharges to surface water wastewaters from other processes. Based According to the data submitted by the regulated under NPDES or POTW on information supplied by the facility, facility, the primary constituents of regulations). We believe these wastes we estimated that the washout water concern in these wastewaters are are sufficiently regulated such that would be diluted at least a hundred-fold hydrochloric acid and phosphorous by the daily throughput to the mismanagement is unlikely. Thus, we acid, which are readily controlled via wastewater treatment system. Any propose not to list these seven waste neutralization. The management categories. potential releases from the practices for these wastewaters One facility appears to treat initial impoundment after dilution with other washout reactor water in tanks and then wastewaters would be unlikely to result minimize opportunities for the release pass it through a nonhazardous waste in any significant long-term risk. of hydrochloric acid or phosphorous surface impoundment. (All other units Therefore, we believe that this specific acid to the environment in an undiluted used to manage this waste have RCRA waste also does not pose significant or unneutralized state. Table III–23 permits or are exempt from permitting.) threats to human health or the summarizes our information on these While we have no analytical data on the environment. wastewaters.

TABLE III±23.Ð WASTEWATERS FROM PHOSPHORUS TRICHLORIDE PRODUCTION

Number of Waste category reported 1998 Volume Reported hazard Sequential management practices generators (MT) codes

Final washout water from reactor ...... 1 not reported none ...... (1) pretreatment in tanks, (2) POTW. Caustic scrubber water ...... 3 4,236 1 none ...... (1) pretreatment in tanks, (2) POTW or NPDES. Process scrubber water ...... 3 12,528 1 D002 (one facil- (1) pretreatment or neutralized in tanks, ity). (2) POTW or NPDES. 1 Volumes from 1996 or 1997 are included in the totals when the wastes were not generated by a facility in 1998.

We have assessed the management concern exists that warrants listing. We management in existing tank-based practices employed for these wastes and have determined that plausible treatment systems. We believe the determined that no exposure pathway of management would be continued manufacturers have made a

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TABLE III±24.ÐNON-CHARACTERISTIC SOLID WASTES

Number of re- Waste category ported genera- 1998 Volume Reported hazard Management practices tors (MT) codes

Spent filters for product ...... 1 0.1 none ...... industrial Subtitle D landfill. Wastewater treatment sludges ...... 4 1 1,100 none 2 ...... Subtitle D landfill or Subtitle C landfill. 1 Volumes from 1997 are included in the totals when the wastes were not generated by a facility in 1998. 2 One facility reported that this wastewater treatment sludge is occasionally characteristically hazardous for D028 (dichloroethane), and the waste is then sent to a Subtitle C landfill. The dichloroethane is used in a process unrelated to the phosphorus trichloride process of interest in today's proposal.

The phosphorus trichloride product is They do not pose a substantial present levels are so high, we believe this waste filtered to remove PCl4 and PCl5. These or potential hazard to human health or will always exhibit the toxicity compounds produce a slime on the the environment. characteristic. product and are more viscous than the b. Description of the potassium d. Agency evaluation. We propose not product. The facility washes the filters dichromate industry. Potassium to list this waste as hazardous under before sending them to disposal. The dichromate, which has a wide variety of Subtitle C of RCRA. This waste is contaminants are easily washed off industrial uses, was produced by a currently managed as hazardous from because of their ready solubility in single facility in the United States in the point of generation through ultimate water. The spent filters are generated in 1998. The U.S. demand for this disposal because it is characteristically very small volumes. We are proposing chemical is very limited and has mostly hazardous. The composition of the not to list them because we do not been replaced by sodium dichromate for waste is such that it is likely to always expect the washed filters to contain industrial use. Any demand not met by be characteristic for chromium. The significant levels of contaminants of the U.S. facility is met by imports to rules applying to characteristic wastes concern. U.S. distributors. Potassium dichromate adequately protect against All four of the facilities that generate is produced by reacting chromium mismanagement. wastewater treatment sludges trioxide with potassium hydroxide. The 11. Sodium Chlorate commingle wastewaters from PCl3 reactants are mixed in a reactor along production with wastewaters from other with a crystal modifier. The potassium a. Summary. We propose not to list processes. The wastewater contribution dichromate is crystallized, sent through any wastes from the production of from the phosphorus trichloride process a centrifuge to remove any remaining sodium chlorate (NaClO3) as hazardous is very small compared to volumes of mother liquor, dried and packaged for under Subtitle C of RCRA. Process wastewaters from the other processes. sale. The single waste is filtered out sludges, spent filters, wastewaters and Therefore, the phosphorus trichloride from the mother liquor. The mother hydrogen gas are generated from the process does not contribute significant liquor is recycled back into the process. production of sodium chlorate. These amounts of constituents to this sludge. c. What kinds of wastes are generated wastes and materials are managed in a We do not believe any of these by this process? There is one waste variety of ways. After analysis of the materials warrant listing as hazardous category generated from this process: management practices and potential wastes from the production of filter solids and spent filter media. exposure pathways of these wastes and phosphorus trichloride. Therefore, we According to data submitted by the materials, we concluded that there are propose not to list these wastes as facility, this waste typically contains no risk pathways of concern. These hazardous wastes under RCRA in this 12.5 percent chromium. The facility wastes and materials do not meet the rulemaking. reports the waste as hazardous for criteria set out at 40 CFR 261.11(a)(3) for chromium and manages it as hazardous listing as hazardous. They do not pose 10. Potassium Dichromate (D007). The reported waste volume for a substantial present or potential hazard a. Summary. We evaluated the wastes 1998 was 0.6 MT. The waste is stored to human health or the environment. from the production of potassium on-site in drums and is shipped off-site b. Description of the sodium chlorate dichromate and propose not to list any to a commercial Subtitle C facility for industry. There were ten facilities wastes from this process as hazardous stabilization to meet the land disposal producing sodium chlorate in 1999. wastes under RCRA. These wastes do restrictions (40 CFR 268.40 and 268.48) This industry manufactures sodium not meet the criteria set out at 40 CFR and final disposal in a Subtitle C chlorate crystals and solutions from 261.11(a)(3) for listing as hazardous. landfill. Because the total chromium electrolysis of a sodium chloride brine.

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Sodium chlorate is the raw material lead. The sodium chlorate industry in Scrubber waters and filtrates are piped used for the production of chlorine general characterizes wastes that have to on-site sodium chlorate production dioxide, which is replacing chlorine and been in contact with chromium or lead units for use. Because these materials sodium hypochlorite to be used as an as hazardous (D007 or D008). Chromium are managed prior to reuse in ways that oxidizing bleaching agent by the pulp is introduced into the process by the present low potential for releases to the and paper industry. The replacement of addition of sodium dichromate into environment, and because we evaluated elemental chlorine with chlorine electrolytic cells to protect electrodes process wastes generated after they are dioxide reduces effluent emissions of from corrosion and to improve product reused, we do not believe that these dioxin formed in the bleaching process yields. The presence of lead in the secondary materials present significant of paper and pulp. Approximately wastes results from the deterioration of threats. At all ten facilities, hydrogen ninety-eight percent of sodium chlorate anodes that can be used in the gas is produced by the electrolysis units is used to generate chlorine dioxide. electrolytic cells. The six waste and is either piped to on-site boilers, The other important use of sodium categories are: vented, or in one case, piped to a chlorate is as an intermediate in the —Process sludges with chromium or compression plant where it is production of other chlorates, lead. These include electrolytic cells compressed and sold. Because the perchlorates, and chlorites. sludge, product filter press sludge, material is a gas produced from a All ten facilities use a similar process and those brine treatment sludges production unit rather than a waste in producing sodium chlorate. These generated from purification where management unit and is conveyed to its facilities dissolve sodium chloride salt brine is formed by mixing salts with destination via piping, the gas is not a in water to create a liquid brine. The chrome-laden wastewaters recycled solid waste. RCRA Section 1004(27) brine is treated to remove impurities, from various steps of the process. excludes non-contained gases from the such as calcium carbonate and —Process sludges without chromium definition of solid waste and thus they magnesium hydroxide. The treated and lead. These wastes include filter cannot be considered a hazardous brine is filtered and pumped into press sludge or drum sludge from waste. (See 54 FR 50973) Because the electrolytic cells. In the cells, sodium treatment of brine, when recycled gaseous materials are not solid wastes chloride is converted to chlorine and chrome-laden wastewater is not used when produced, we did not evaluate sodium hydroxide which further react in the brine dissolution step. them further for purposes of listing. to form sodium chlorate and hydrogen —Spent filters with chromium or lead. One facility reports generating a gas. This reaction is catalyzed by The filters are generated at several wastewater (sulfate solution) from brine sodium dichromate. Sodium chlorate is points in the production process, but treatment. The wastewater is then treated with heat and urea to most are generated after the transported to an off-site facility and remove residual sodium hypochlorite. electrolysis of the brine solution when used in their black liquor pulping Sodium chlorate is then processed the mother liquor is filtered to remove process. The sulfate solution is added to further for crystallization, centrifuging, impurities. black liquor for use in a wood digester. drying, and packaging. A more complete —Spent filters without chromium and The process in the digester is outside discussion of this process and the lead. Examples include disposable the scope of the consent decree and we industry can be found in ‘‘Sodium cartridge and sock filters from have not evaluated risks from wastes Chlorate Listing Background Document treatment of brine, when recycled that it produces. We note, however, that for the Inorganic Chemical Listing chrome-laden wastewater is not used the reuse of black liquor is excluded Determination’’ in the docket for today’s in the brine dissolution step. from regulation (40 CFR 261.4(a)(6)). proposal. —Wastewaters with chromium that are The sulfate solution is stored in tanks c. What kinds of wastes are generated not recycled back to the process. prior to use in the pulping process, by this process? Wastes generated from —Other wastewaters that do not contain which minimizes the potential for the production of sodium chlorate chromium or lead and are not releases. consist of process sludges, spent filters recycled (condensate, cooling water, and ion-exchange wastewater). How Are These Wastes Currently Being and wastewaters. Based on an Managed? evaluation of survey responses from the In addition to these wastes, other ten sodium chlorate producers, we materials are produced by all ten Table III–25 summarizes the six waste divided the wastes further into six facilities during the production of categories, waste characteristics, waste general waste categories based on the sodium chlorate that are piped directly volumes, and their current management presence or absence of chromium and back to the production process. practices:

TABLE III±25.ÐWASTE FROM SODIUM CHLORATE PRODUCTION

1 1998 Volume Waste category (number of facilities) Reported Waste Codes (MT) Management practices

Process sludges with chromium or lead D001, D002, D007, D008 ...... 28,547 Nine facilities store the waste on site in (10). containers and then send it to Subtitle C landfills or incinerators; one facility decharacterizes the waste in tanks be- fore managing it in on-site surface im- poundments. Two facilities did not re- port hazard codes.

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TABLE III±25.ÐWASTE FROM SODIUM CHLORATE PRODUCTIONÐContinued

1 1998 Volume Waste category (number of facilities) Reported Waste Codes (MT) Management practices

Process sludges without chromium and none reported ...... 1,886 Three facilities store the waste on site in lead (5 2). containers and then send it off-site to municipal Subtitle D landfills; one facil- ity stores the waste on a concrete pad with secondary containment before applying it to an on-site land farm; one facility stores the waste on site in con- tainers and then sends it off-site to an industrial Subtitle D landfill; one facility stores the waste on site in containers before sending it off-site for recycling. Spent filters with chromium or lead (7) ... D001, D007, D008 ...... 82.9 All seven facilities classify the waste as hazardous; six send the waste to Sub- title C landfills or incinerators; one fa- cility decharacterizes the waste on-site in tanks, stores it in a closed com- pactor, then ships the waste off-site to an industrial Subtitle D landfill. Spent filters without chromium and lead none reported ...... 3.52 Three facilities store the waste on site in (4). containers and send it off-site to Sub- title D landfills. One facility stores the waste with process sludge in on-site containers and then sends it off-site to a Subtitle C facility for stabilization prior to disposal in a Subtitle C landfill. Wastewaters with chromium that are not D002, D007 ...... 26,736 One facility sends the wastewater to an recycled back to the process (2). off-site Subtitle C facility for treatment and disposal. One facility combines and treats the wastewater with other process wastewaters in tanks prior to discharge to on-site surface impound- ments. Other wastewaters that do not contain none reported ...... 10,744 3 Discharged via NPDES permit or to a chromium or lead and are not recycled POTW. (condensate, cooling water, ion-ex- change wastewater). 1 D001 (ignitability); D002 (corrosivity); D007 (chromium); D008 (lead). 2 One facility contributes more than one residuals to this waste group. 3 Two facilities did not report volumes of this wastewater.

d. Agency evaluation. We selected generate this waste. Seven facilities How Was This Waste Characterized? wastes from three facilities for sampling. classify their wastes as characteristic We collected a total of six samples to As described in detail in ‘‘Sodium and send it off-site to Subtitle C landfills assess this waste categories. Three Chlorate Listing Background Document or incinerators. Two facilities do not samples of the sludge from electrolytic for the Inorganic Chemical Listing classify their wastes as characteristic but cells were collected at two facilities Determination’’ in the docket for today’s nevertheless send their wastes to where the wastes were destined for proposal, we selected these facilities Subtitle C landfills. Subtitle C treatment and disposal. These and wastes because based on the survey The tenth facility, located in two facilities generate and manage this information collected, we believe that waste as characteristically hazardous. the wastes generated by these three Hamilton, Mississippi, reports this waste to be characteristic and treats it in These samples were part of the record facilities are fully representative of the characterizing this waste category, but wastes generated by this industry and tanks to reduce hexavalent chromium to the relatively stable trivalent state. The were not used for risk assessment. their management practices. We collected another three samples We evaluated the characteristics and facility commingles this sludge with wastes from the production of titanium from the Hamilton, Mississippi facility current management practices of each of that classifies this waste as dioxide (TiO ) in these tanks. The the six waste categories. The details of 2 characteristically hazardous and treats it treated mixture is subsequently our evaluation follow. in tanks to remove the characteristic (1) Process sludge with chromium or managed in a series of four surface prior to pumping the effluent to on-site lead. impoundments, three of which are lined surface impoundments. One sample with leachate collection systems. How Is This Waste Managed? (KM–SC–01) reflects the untreated Today’s proposal separately addresses sodium chlorate sludge collected from a The predominant source of process the titanium dioxide wastes that are dedicated sump prior to commingling sludge with chromium or lead is from commingled with this sodium chlorate with the titanium dioxide wastewaters. the periodic cleanout of electrolytic sludge (see section III.F.14.c.(14)). The second sample (KM–SI–01) is the cells used to convert the brine solution treated combined wastes collected at the to sodium chlorate. All ten facilities inlet to the surface impoundments. The

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TABLE III±26.ÐANALYTICAL DATA FOR SODIUM CHLORATE

KM±SC±01 KM±SI±01 KM±SI±04 (Untreated (Treated commingled (Treated commingled NaC1O3 NaC1O3 and TiO2 wastes) NaC1O3 and TiO2 sludge Constituents of concern wastes only) in impoundment) HBL Total Total SPLP Total SPLP (mg/1) (mg/kg) (mg/l) (mg/kg) (mg/l)

Chromium ...... 0.99 31.1 <0.05 1,140 0.05 23 Hexavalent Chromium ...... 0.85 L <0.02 <0.02 <0.8 0.03 0.05 L: Concentration reported from analysis performed outside method recommended holding time. Value should be considered biased low.

The total chromium concentration in characteristic hazardous wastes) treats (2) Process sludge without chromium the treated waste is higher than the the sludge in tanks to reduce hexavalent and lead. untreated waste due to commingling chromium to trivalent chromium prior with other wastes from the titanium to placement in on-site surface How Is This Waste Managed? dioxide production process. There are impoundments. We found that the This sludge is produced as part of the other constituents detected in the waste did not pose risks during initial purification of the brine solution. treated commingled waste sample (KM– treatment because there are no exposure Five facilities report generating this type SI–01) that are attributable to the pathways of concern for the on-site of waste and managing it as titanium dioxide production process; treatment tanks. The wastes are treated nonhazardous. Four facilities manage these constituents are assessed in in concrete tanks with secondary the waste in an on-site land farm, off- containment which minimize potential section III.F.14.c.(14) of today’s site municipal Subtitle D landfills, and releases to groundwater. We also are not proposal. an industrial Subtitle D landfill. One concerned with potential air releases What Is EPA’s Listing Rationale for This facility ships their waste off-site for from these tanks as neither volatile recycling. Waste? contaminants nor airborne particulates We propose not to list this waste are likely to be present in the wastes. As We collected a total of four samples category. Seven facilities consider discussed above, the primary of this waste category from two wastes in this category to be constituent of concern in this waste is facilities. Two of the four samples (HT– characteristically hazardous (for D001, hexavalent chromium, which is treated SN–01 and EC–SN–03) are D002, D007 or D008) and manage the to form relatively stable trivalent representative of wastes that are land wastes under Subtitle C regulations. We chromium. The physical form of the disposed. The other two samples (EC– believe that these regulations adequately wastes (i.e., sludge with high water SN–01 and EC–SN–02) are protect against mismanagement. Two content) eliminates the potential for a representative of wastes that are facilities do not classify their wastes as significant release of airborne generally recycled and occasionally also characteristic but send them to Subtitle particulates. Furthermore, our analytical landfilled. Table III–27 identifies the C landfills. We also believe that this data show that the waste, after constituents of concern that we found to practice adequately prevents treatment, does not contain any be present in the waste at levels mismanagement. The remaining facility constituents of concern at levels exceeding their respective HBLs and/or (which does not identify its sludges as exceeding health-based levels. soil screening levels. TABLE III±27.ÐANALYTICAL RESULTS FOR SODIUM CHLORATE PROCESS SLUDGE WITHOUT CHROMIUM AND LEAD (PPM)

HT±SN±01 EC±SN±03 EC±SN±01 EC±SN±02 Parameter HBL 1SSL Total TCLP SPLP Total TCLP SPLP Total TCLP SPLP Total TCLP SPLP

Arsenic ...... 14.3 20.03 <0.05 <5 <0.005 <0.05 <5 <0.005 <0.05 <5 <0.005 <0.05 0.0007 5.2 Cadmium ...... 27.4 <0.05 <0.05 <5 <0.05 <0.05 <5 <0.05 <0.05 <5 <0.05 <0.05 0.0078 4.3 Chromium ...... 57.3 <0.05 <0.05 15.3 <0.05 <0.05 <5 <0.05 <0.05 10.1 <0.05 <0.05 23 37 Copper ...... 17.2 <0.25 <0.05 15.3 <0.05 <0.05 <5 <0.25 <0.05 5.3 <0.25 <0.05 1.3 17 Lead ...... 14.8 0.024 <0.03 139 <0.03 <0.03 19.3 0.12 E 0.001 34.9 0.05 E 0.002 E 0.015 400* Manganese ...... 69.2 0.08 <0.05 238 4.5 <0.05 125 0.5 <0.05 51.9 0.7 <0.05 0.73 330 Mercury ...... 0.5 L <0.002 <0.0002 <0.1 <0.002 <0.0002 <0.1 <0.002 <0.0002 <0.1 <0.002 <0.0002 0.0047 24* Nickel ...... 7.4 <0.2 <0.05 12.1 0.4 <0.05 <5 <0.2 <0.05 <5 <0.2 <0.05 0.31 13 Silver ...... 1.1 <0.1 <0.01 <1 <0.1 <0.01 <1 <0.1 <0.01 <1 <0.1 <0.01 0.078 400* Zinc ...... 111 <2 <0.5 279 10.6 <0.5 <50 <2 <0.5 <50 <2 <0.5 4.7 48

1 SSL: Soil Screening Level based on geometric mean background concentration (mg/kg) in soils in conterminous U.S. or soil ingestion HBL (marked *). 2 Results are less than the typical laboratory reporting limit, but are greater than the calculated instrument detection limit. E: Analysis performed outside recommended holding time. Reported value should be considered as estimated.

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What Management Scenarios Did We treatment scenario. Finally, we We used the SPLP results of all four Aassess? compared the total concentrations of relevant samples to evaluate the We evaluated wastes managed under copper, lead, mercury, and silver of all industrial Subtitle D landfill the four identified management samples to the soil ingestion HBL management scenario. We found that scenarios: on-site land farm, municipal because these constituents were not the waste poses no substantial present Subtitle D landfill, industrial Subtitle D assessed in the chlorinated aliphatics or potential hazard to human health and landfill, and recycling. risk analyses. The maximum total the environment when managed in an Land farm scenario. One facility concentrations of lead, mercury, and industrial Subtitle D landfill because the reports managing 37 MT/year of this silver are well below the soil ingestion SPLP leachate concentration of all waste in an on-site permitted land farm. HBL, and the maximum total constituents of the four samples of this EPA previously assessed this same land concentration of copper in this waste waste category are below their farm as part of the chlorinated aliphatics (i.e., 17.2 mg/kg) is very close to the soil respective HBLs. ingestion HBL (i.e., 17 mg/kg). We listing determinations (see proposed We used the TCLP results of all four believe that after mixing with soil in the rule at 64 FR 46475, August 25, 1999). relevant samples to assess the municipal Today’s assessment of sodium chlorate land application unit, the copper Subtitle D landfill scenario. We waste placed in the same unit is based concentration in the unit will be even modeled all three volumes reported on our earlier modeling of this unit for lower. We do not believe this waste being sent to municipal Subtitle D a waste from the production of poses risk via volatilization to the air chlorinated aliphatics (EDC/VCM pathway because it does not contain any landfills. We focused our assessment on sludges). significant toxic volatile chemicals. In the geological regions in the In assessing this management addition, the comparison described northwestern and southeastern areas of scenario, we first compared the total above for this unit, where we the country because of the locations of constituent concentrations of all four determined that the detected waste the facilities and the landfills currently record samples to background soil constituents are present in the waste at being used. The constituents we concentrations. The following metals levels below or very close to the soil modeled are arsenic, lead, manganese, exceeded this screening criteria: arsenic, ingestion levels, suggests that any wind nickel, and zinc. The details regarding cadmium, chromium, copper, lead, blown dust from the unit should not our modeling inputs and assumptions mercury, silver, and zinc. We then used pose risk at levels of concern. are provided in ‘‘Sodium Chlorate the metal modeling results generated Based on our analysis, we conclude Listing Background Document for the from the chlorinated aliphatics listing that the waste does not present a Inorganic Chemical Listing determination to calculate the substantial risk to human health or the Determination’’ and ‘‘Risk Assessment proportional sodium chlorate risk. The environment when land applied. for the Listing Determinations for calculated modeling results of arsenic, Landfill scenarios. Three facilities Inorganic Chemical Manufacturing cadmium, hexavalent chromium, and manage their wastes in municipal Wastes’ in the docket for today’s zinc for the same land farm are all Subtitle D landfills and one facility proposal. The results of our risk below a hazard quotient (HQ) of 1 and manages its waste in an industrial assessment are summarized below in 10¥6 risk thresholds for the land Subtitle D landfill. Table III–28.

TABLE III±28.ÐGROUNDWATER PATHWAY RISK ASSESSMENT RESULTS FOR PROCESS SLUDGE WITHOUT CHROMIUM AND LEAD

Arsenic Manganese Nickel Zinc Percentile Adult can- Child can- cer risk cer risk Adult HQ Child HQ Adult HQ Child HQ Adult HQ Child HQ

90th ...... 3E±08 ...... 2E±08 ...... 2E±04 ...... 4E±04 ...... 2E±06 ...... 3E±06 ...... 5E±08 ...... 1E±07 95th ...... 2E±07 ...... 2E±07 ...... 6E±04 ...... 1E±03 ...... 2E±05 ...... 3E±05 ...... 5E±06 ...... 1E±05

Based on these risk assessment Determinations for Inorganic Chemical the off-site facility. We believe that the results, we conclude that process sludge Manufacturing Wastes’’ in the docket for constituent concentrations in the final without chromium and lead does not this proposal. cement product would be even lower pose a substantial present or potential Recycling scenario.—One facility due to mixing with other materials. hazard to human health and the ships their wastes to an off-site facility What Is EPA’s Listing Rationale For environment when managed in for reuse. The material is added to This Waste? municipal Subtitle D landfills. We mined gypsum used to retard the setting calculated hazard quotients for non- of concrete. We assessed this use Based on our assessments of the four carcinogenic compounds (lead, because it involves land placement, management scenarios (on-site land manganese, nickel, and zinc), and all of with higher likelihood of releases to the farm, municipal Subtitle D landfill, these were well below a value of one. environment. Two samples of this waste industrial Subtitle D landfill, and We found no adult or child cancer risk category were collected from the facility recycling), we found that the wastes do for arsenic in excess of 1E–06 at the that produces and manages this waste in not present a substantial risk to human 95th percentile. Based on these results such a fashion. We compared this use to health or the environment. Therefore, we conclude that this waste does not a less protective landfarming scenario, we propose not to list these wastes. pose risk to human health and the which we modeled, and found no risk environment. For a more complete of concern. The volume of the waste is (3) Spent filters with chromium or description of this analysis, see ‘‘Risk quite small (<1%) when compared to lead. Assessment for the Listing the volume of mined gypsum used by

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How Is This Waste Managed? UTS) before being landfilled at an off- spent filter sample (KM–FB–01) for site industrial Subtitle D landfill. arsenic, lead, total chromium, and Spent filters are generated at several How Was This Waste Characterized? hexavalent chromium. Chromium and points in the production process but lead are the two primary constituents of most are generated after the electrolysis We collected one sample of the spent concern in wastes of this category. The of the brine solution. Seven facilities filter that was decharacterized prior to sample was not collected from the report generating this waste. Six of the being sent to an industrial Subtitle D facility that uses anodes with lead seven facilities report this waste to be landfill. We did not sample any of the coating, thus lead was not present in characteristic and ship it to off-site six facilities that already adequately this sample. Arsenic was the only Subtitle C landfills or incinerators. The managed the waste under Subtitle C seventh facility generates a very small regulations. Table III–29 presents the constituent detected in the SPLP volume of D007 waste that is acid- analytical results for the total and analysis of this sample at levels washed and decharacterized (to meet leaching analyses of the decharacterized exceeding the HBL.

TABLE III±29.ÐANALYTICAL RESULTS FOR SPENT FILTERS WITH CHROMIUM (KM±FB±01)

Total TCLP SPLP Drinking water Parameter (mg/kg) (mg/l) (mg/l) HBLs (mg/l)

Arsenic ...... <0.5 <0.5 10.005 0.0007 Chromium ...... 41.0 <0.05 <0.05 20 Hexavalent Chromium ...... 16.8 2NA 2<0.022 0.05 Lead ...... <5 <0.5 <0.03 0.015 1 Results are less than the typical laboratory reporting limit, but are greater than the calculated instrument detection. 2 NA Not applicable. Typical TCLP leaching solution is not suitable for leachable hexavalent chromium because most (or all) hexavalent chro- mium in TCLP waste leachates were converted to trivalent chromium. The leach test for hexavalent chromium was modified by replacing the typ- ical (TCLP/SPLP) solution with deionized water.

What Is EPA’s Listing Rationale For concern. For a more complete type of waste. Two of these four This Waste? description of this analysis, see ‘‘Risk facilities manage their wastes as Assessment for the Listing As previously noted, six of the seven nonhazardous in municipal Subtitle D Determinations for Inorganic Chemical generators of this waste report managing landfills. One facility manages its waste Manufacturing Wastes’’ in the docket for their wastes in Subtitle C facilities as as nonhazardous in an industrial this proposal. characteristically hazardous from the Subtitle D landfill. One facility sends Our analytical data demonstrate that their spent filters along with process point of generation through ultimate the waste is effectively decharacterized disposal. We did not conduct risk sludge off-site to a Subtitle C facility for and does not pose risks warranting stabilization prior to disposal in a assessment on wastes identified as listing for chromium, the primary hazardous wastes and managed in Subtitle C landfill. These wastes are constituent of concern in this waste. generated in very small volumes. Subtitle C facilities because listing The result of the screening analysis for would not provide any significant arsenic, the only constituent present in How Was This Waste Characterized? incremental control of wastes already the waste’s leachate at levels exceeding managed under Subtitle C. We the HBL, shows that the arsenic in this We collected two samples (HT–FB–01 evaluated the small volume waste (i.e., waste does not pose risk to human and HT–FB–02) from one facility. These 2.3 MT/yr) generated by the seventh health and the environment. Therefore, two samples are representative of wastes facility that decharacterizes its waste we propose not to list spent filters with in this category that are land disposed. before landfilling in an industrial chromium. We found that antimony, arsenic, boron, Subtitle D landfill. (4) Spent filters without chromium hexavalent chromium, and lead in the Because the volume of this waste is and lead. TCLP or SPLP waste leachates exceeded relatively small, we used a screening their HBLs. We also found that analysis (described in section III.E.3) to How Is This Waste Managed? cadmium was not detected in the screen the potential risk to groundwater This residual is usually generated as leachates at a detection level of six associated with landfilling this waste. part of the initial brine purification times higher than its HBL. The detection We found that the SPLP data for arsenic steps, where impurities are removed limit was high due to dilution to screens out because the volume of the from the brine solution, and from minimize sample matrix interferences. waste generated by the facility is filtering of product during packaging. Information on constituents of concern insufficient to release arsenic at levels of Four facilities report generating this is summarized in Table III–30.

TABLE III±30.ÐANALYTICAL RESULTS FOR SPENT FILTERS WITHOUT CHROMIUM OR LEAD

HT±FB±01 HT±FB±02 HBL Parameter Total TCLP SPLP Total TCLP SPLP (mg/l) (mg/kg) (mg/l) (mg/l) (mg/kg) (mg/l) (mg/l)

Antimony ...... 34.1 0.018 <0.005 <5 0.012 <0.005 0.006 Arsenic ...... 7.3 0.014 0.003 5.3 <0.005 <0.005 0.0007 Boron ...... <50 6.1 <0.05 <50 0.67 <0.5 1.4 Cadmium ...... 22.5 <0.05 <0.05 <5 <0.05 <0.05 0.008 Cr, +6 ...... <0.8 NA <0.02 2.8 L NA 0.19 L 0.05

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TABLE III±30.ÐANALYTICAL RESULTS FOR SPENT FILTERS WITHOUT CHROMIUM OR LEADÐContinued

HT±FB±01 HT±FB±02 HBL Parameter Total TCLP SPLP Total TCLP SPLP (mg/l) (mg/kg) (mg/l) (mg/l) (mg/kg) (mg/l) (mg/l)

Lead ...... 8.7 0.024 0.06 7.1 0.020 0.012 0.015 L: Concentration reported from analysis performed outside required holding time. Value should be considered biased low.

What Management Scenarios Were below in Table III–31, suggest that the What Are the Results of EPA’s Risk Assessed? only constituent of concern that Assessment for This Waste When We modeled both the industrial (0.6 required modeling (arsenic) does not Managed in Municipal Subtitle D MT/year) and municipal (2.8 MT/year) pose a substantial present or potential Landfills? landfill scenarios, based on the reported hazard to human health and the management practices. environment. We found no arsenic Our risk assessment results for the We used the SPLP leachate cancer risk in excess of 1E–08 at the municipal landfill scenario, concentrations to evaluate the industrial 95th percentile for either adult or child summarized below in Table III–32, landfill scenario. The constituents of exposure scenarios. Therefore, we suggest that the three constituents of concern that exceeded their respective believe that this waste when managed in concern (antimony, arsenic, and HBLs in the SPLP results were arsenic, industrial Subtitle D landfills clearly cadmium) do not pose a substantial hexavalent chromium, and lead. We does not warrant listing. For a more present or potential hazard to human evaluated these constituents using the complete description of this analysis, health and the environment. The hazard de minimis volume screening analysis, see ‘‘Risk Assessment for the Listing quotients, for both the adult and child as described in section III.E.3 of today’s Determinations for Inorganic Chemical exposure scenarios, of antimony are less proposal. The analysis suggests that Manufacturing Wastes’’ in the docket for than 0.01 at the 95th percentile, and of hexavalent chromium and lead are not this proposal. cadmium, are less than 0.001 at the 95th of concern. We then modeled arsenic percentile. We found no arsenic cancer using our standard groundwater model TABLE III±31.ÐRISK RESULTS FOR risk in excess of 1E–08 at the 95th for the industrial landfill scenario. percentile for either adult or child We used the TCLP leachate FILTERS WITHOUT CHROMIUM AND exposure scenarios. Therefore, we concentrations to evaluate the LEADÐINDUSTRIAL SUBTITLE D believe that this waste when managed in municipal landfill scenario. Using the LANDFILL SCENARIO de minimis volume analysis, we municipal Subtitle D landfills does not screened out boron, hexavalent Arsenic warrant listing. For a more complete description of this analysis, see ‘‘Risk chromium, and lead. We then Percentile Adult can- Child can- Assessment for the Listing conducted full groundwater modeling cer risk cer risk for the municipal scenario for antimony, Determinations for Inorganic Chemical Manufacturing Wastes’’ in the docket for arsenic, and cadmium. 90th ...... 1E±09 8E±10 this proposal. What Are the Results of EPA’s Risk 95th ...... 5E±09 4E±09 Assessment for This Waste When Managed in an Industrial Subtitle D Landfill? Our risk assessment results for the industrial landfill scenario, summarized

TABLE III±32. RISK RESULTS FOR FILTERS WITHOUT CHROMIUM AND LEAD MUNICIPAL SUBTITLE D LANDFILL SCENARIO

Antimony Arsenic Cadmium Percentile Adult can- Child can- Adult HQ Child HQ cer risk cer risk Adult HQ Child HQ

90th ...... 5E±04 1E±03 5E±10 4E±10 3E±05 6E±05 95th ...... 2E±03 4E±03 5E±09 4E±09 1E±04 3E±04

(5) Wastewaters with chromium that electrolytic cells, the excess caustic metals on the surface. The facility are not recycled back to the process. from the hydrogen purification step, and combines the wastewaters with the the wastewater from the production of How Is This Waste Managed and How wastewaters from its titanium dioxide sodium chlorate crystals. The facility Is It Characterized? production process and treats the stores the wastewater on-site in closed commingled wastewaters in tanks. The Two facilities report generating this tanks before sending it off-site to a treated wastewater is then discharged to wastewater and characterize it as hazardous waste facility for treatment on-site surface impoundments. hazardous (D002 and D007). One facility and disposal. The other facility generates 11 MT per year of this generates 26,725 MT per year of this wastewater from its on-site laboratory wastewater from acid washing filters testings of the electrolyte in the and anodes to remove buildup of trace

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What Is EPA’s Listing Rationale for This facility provide sufficient structural The two facilities’ processes diverge Waste? integrity and have secondary significantly at this point. At the Texas One facility identifies the waste as containment areas to minimize potential facility, the sodium chromate solution is hazardous and manages it in accordance releases to groundwater. We are either crystallized and sold or processed with Subtitle C regulations. We believe unlikely to find potential air releases electrolytically to convert the sodium from these tanks or the permitted that applicable Subtitle C regulations chromate to sodium dichromate. The facility as neither volatile contaminants adequately protect against electrolytic cell system also produces nor airborne particulates are likely to be mismanagement, and we did not sodium hydroxide solution which, the present in these wastewaters. investigate it further. facility reports, they sell. The North For the other facility, in Hamilton, 12. Sodium Dichromate Carolina facility converts the sodium Mississippi, we evaluated its combined chromate solution to sodium a. Summary. We have evaluated the dichromate through acidification, and wastewaters and solids as described wastes, waste management practices, above in the ‘‘process sludges with the sodium dichromate is then partially and potential risk exposure pathways evaporated. The acidification process chromium or lead’’ category. Today’s associated with the sodium dichromate proposal separately addresses the also produces sodium sulfate and lower production processes and propose not to purity sodium sulfate ‘‘saltcake,’’ both titanium dioxide wastes that are list any wastes from this industry as commingled with this sodium chlorate of which the facility sells. The sodium hazardous wastes under Subtitle C of dichromate is then either used in liquid waste. We propose not to list these RCRA. These wastes do not meet the wastes. form or further evaporated to produce a criteria listed under 40 CFR 261.11(a)(3) crystalline product. (6) Other wastewaters that do not for listing a waste as hazardous. They do c. How does the Bevill Exclusion contain chromium or lead and are not not pose a substantial present or apply to wastes from the sodium recycled. potential threat to human health or the dichromate manufacturing processes? environment. We have identified no How Is This Waste Managed? The sodium dichromate manufacturing risks of concern associated with the facilities produce two types of residuals There are other wastewaters generated current management of these wastes. which are eligible for the Bevill from several points of the process, Note that certain wastes from this sector exemption once disposed: beneficiation including process condensate, cooling are exempt mineral processing wastes wastes (See 40 CFR 261.4(b)(7)(i)) and waters, and ion-exchange wastewater. which are not within the scope of Four facilities reported generating these today’s listing proposal. mineral processing wastes referred to as wastewaters. Two facilities generate b. Description of the sodium treated residue from roasting/leaching of process condensates from condensing dichromate industry. Two facilities in chromium ore (see 40 CFR water vapor from their crystalizers, the United States produce sodium 261.4(b)(7)(ii)(N)). steam jets, or pad water evaporator. dichromate; one in North Carolina and Under the Bevill exemption, any Both facilities store their process one in Texas. Both facilities sell their wastes generated from beneficiation of condensates in closed tanks. One product on the open market in addition ores, such as crushing, mixing, and facility neutralizes the condensate prior to using the material as a feedstock for milling, are Bevill exempt. Both to discharging it to an NPDES permitted various manufacturing processes on- facilities beneficiate ore by drying and outfall. The other facility does not treat site. The majority of sodium dichromate grinding chromite ore and mixing the the condensate, but tests to ensure it is used as a feedstock for the production ore with other ingredients prior to meets its State Pollutant Discharge of chromic acid. It is also used in a wide placement in the roasting kiln and Elimination System permit prior to variety of other uses. For more detailed generate air pollution control dusts from discharge to a river. One facility information concerning this industry, these processes. However, the residuals generates wastewater from regeneration see ‘‘Sodium Dichromate Listing from these processes, which would be of the ion-exchange unit that is used for Background Document for the Inorganic Bevill exempt, are not disposed of but purification of the brine. The Chemical Listing Determination’’ in the rather captured and returned to the wastewater is collected in a tank for pH docket for today’s proposal. process from which they originated for neutralization before it is discharged to The two sodium dichromate chromium recovery. a POTW. One facility generates production facilities use somewhat In terms of when beneficiation stops wastewater from cooling tower different manufacturing processes and and mineral processing starts, EPA blowdown, chemical storage tank generate somewhat different wastes. determined in 1989 that the roasting/ scrubber pad, hydrogen scrubber pad, Both facilities use imported chromite leaching of chromium ore to produce and water demineralization area. These ore as their primary feedstock. They dry sodium chromate is mineral processing wastewaters are piped to its on-site and grind the ore and feed it into a rather than beneficiation. 54 FR 36592 NPDES facility to be processed and roasting kiln or hearth with other (September 1, 1989) stated: discharged. materials such as soda ash, lime, and ‘‘A specific exception to the above sodium hydroxide. The facilities roast, categorization system applies when the What Is EPA’s Listing Rationale for This then quench and leach the ore with Waste? roasting/leaching sequence produces a final water, producing sodium chromate or intermediate product that does not We propose not to list these solution and solid ore residues. Both undergo further beneficiation or processing wastewaters as hazardous. We evaluated facilities return the ore residues to the steps (e.g., the leach liquor serves as an input these wastewaters that are stored and manufacturing process for further to inorganic chemical manufacturing). In this treated in tanks or in a NPDES roasting and leaching. The facilities type of situation, the Agency believes that the permitted facility. We found that these purify the resulting sodium chromate operation is most appropriately considered a processing, rather than a beneficiation, wastewaters do not pose risks solution product stream by adjusting its operation. In the context of this rulemaking, warranting regulation during treatment pH, treating it with sodium carbonate, one candidate Bevill waste (roast/leach ore because there are no exposure pathways and, at the Texas facility, sodium residue from primary chrome ore processing) of concern. The wastewater treatment dichromate, and filtering out the is affected by this distinction; EPA believes tanks and the wastewater treatment resulting solid impurities. that this material is clearly a waste from

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TABLE III±33.ÐSODIUM DICHROMATE PRODUCTION RESIDUALS

1998 volumes Reported waste Waste category (MT) codes Sequential management practices

North Carolina Facility

Residuals commingled in spent ore residue treat- ment unit 1: Spent post-neutralization ore residue (Bevill ex- 146,937 ...... D007 ...... Sent on-site to tank-based spent ore residue treat- empt after treatment). ment unit with NPDES permitted discharge. Spent post-leach ore residue (Bevill exempt 25,930 ...... D007 ...... Sent on-site to tank-based spent ore residue treat- after treatment). ment unit with NPDES permitted discharge. Saltcake drier scrubber wastewater ...... 13,851 ...... D007 ...... Sent on-site to tank-based spent ore residue treat- ment unit with NPDES permitted discharge. boiler washout (Bevill exempt after 70 ...... D007 ...... Sent on-site to tank-based spent ore residue treat- treatment). ment unit with NPDES permitted discharge. Residuals disposed of on-site: Reduced chromium treatment residues (com- 129,503 ...... None ...... Sent to on-site industrial Subtitle D disposal unit. mingled Bevill exempt and non-exempt resi- dues). Commingled treated wastewaters (commingled 920,161 ...... None ...... Passed through sand filters then discharged directly Bevill exempt and non-exempt residues). under NPDES permit or sent to on-site industrial Subtitle D disposal unit. Residuals disposed of off-site: Chromium-contaminated filters, membranes, 67 ...... D007 ...... Stored in on-site roll-off bin before off-site treatment and other plant waste. and landfill disposal at Subtitle C facility. Spent sand filter sands (commingled Bevill ex- 21.7 (1997) ...... None ...... Stored in on-site drums or roll-off bins before dis- empt and non-exempt residues). posal in off-site industrial Subtitle D landfill.

Texas Facility

Residuals commingled in spent ore residue treat- ment unit: Spent post-neutralization ore residue (Bevill ex- 60,000 ...... D007 ...... Sent to on-site, covered, tank-based, spent ore res- empt after treatment). idue treatment unit with NPDES permitted dis- charge. Caustic filter sludge ...... 80 ...... D002 ...... Sent to on-site, covered, tank-based, spent ore res- idue treatment unit with NPDES permitted dis- charge. Residuals commingled in wastewater treatment unit 2: Sodium dichromate evaporation unit wastewater ∼2,500 ...... None ...... Sent to on-site, tank-based wastewater treatment unit with NPDES permitted discharge. Sodium chromate evaporation unit wastewater ∼300 ...... None ...... Sent to on-site, tank-based wastewater treatment unit with NPDES permitted discharge.

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TABLE III±33.ÐSODIUM DICHROMATE PRODUCTION RESIDUALSÐContinued

1998 volumes Reported waste Waste category (MT) codes Sequential management practices

Residuals disposed of on-site: Reduced chromium treatment residues from 60,000 ...... None ...... Sent to on-site industrial Subtitle D, double-lined spent ore residue treatment unit (commingled surface impoundment for dewatering and dis- Bevill exempt and non-exempt residues). posal. Impoundment has NPDES permitted out- flow. Reduced chromium treatment residues from ∼30,000 (1999) None ...... Sent to on-site industrial Subtitle D, double-lined wastewater treatment unit (commingled Bevill surface impoundment for dewatering and dis- exempt and non-exempt residues). posal. Impoundment has NPDES permitted out- flow. Commingled treated wastewaters (commingled 186,515 ...... None ...... Sent to on-site industrial Subtitle D surface im- Bevill exempt and non-exempt residues). poundment, filtered through sand filters, then dis- charged directly under NPDES permit. Residuals disposed of off-site: Process filters and membranes, baghouse 24 ...... D007 ...... Stored in on-site roll-off box before treatment and bags, chromium-contaminated empty con- landfill disposal at Subtitle C facility. tainers, and other plant wastes. Spent sand filter sands (commingled Bevill ex- ∼2 MT once None ...... Placed in on-site non-hazardous soil waste bin and empt and non-exempt wastes). every two then disposed of in off-site industrial Subtitle D years. landfill. 1 Remediation well water, cooling tower blowdown, and stormwater are also treated in this unit. These materials are beyond the scope of this listing determination. 2 Stormwater and remediation well water are also treated in this unit. Contaminated media are not within the scope of this listing determination.

In addition to these wastes, the disposal). Since these processes are We propose not to list any of the sodium dichromate manufacturers outside the scope of the consent decree wastes from the sodium dichromate produce residuals which are either we did not evaluate any of these manufacturing industry. Many wastes piped back to the production process or materials further. We did however, from this industry are Bevill exempt sold for use in other manufacturing evaluate some residuals produced on- once treated, and therefore not within processes. Air pollution control devices site at the North Carolina and Texas the scope of the consent decree capture materials that are returned to facilities during the preparation of the requirements. Other wastes are their units of origin or to other materials that are sold. See the characteristically hazardous and are manufacturing process units. At the discussions in the sections below of salt managed at permitted Subtitle C North Carolina facility, ore residue cake drier scrubber water and caustic facilities off-site. Some wastes did not washwaters and calcium carbonate filter sludge. Finally, the North Carolina exhibit constituents at levels of concern residuals are returned to the production facility produces some off-specification for purposes of a listing given the nature process for chromium recovery. product, which it reinserts into the of their management and disposal. The Chromium-bearing solution from the sodium dichromate manufacturing main constituent of concern, chromium, saltcake purification process is directly process. Off-specification product, when is treated on-site for many of the wastes. reused in the roasted ore quench, leach reinserted without reclamation into the Several wastes from each of the and filter process. At the Texas facility, process from where it originated, is not facilities are disposed of in a treated chromium-containing residuals from a solid waste. See the ‘‘Sodium form, rather than an as-generated form. scrubbers on the hearth and on the Dichromate Listing Background In general, we focused our evaluation on sodium chromate and dichromate Document for the Inorganic Chemical the treated form of wastes because it is ultimately only the treated wastes evaporation/crystallization units are Listing Determination’’ for more details which are disposed. reused in the hearth kiln and quench on these residuals. tank units. Because these materials are The sections below describe how reused in production units in ways that e. Waste characterization and Agency wastes are generated and managed at the present low potential for release, and evaluation. Chromium is the primary two sodium dichromate manufacturing because we evaluated process wastes constituent of concern in the wastes facilities, each with its own production generated after the secondary material is from both facilities. Chromium occurs process, and our rationale for proposing reinserted into the process, we do not in several production wastes at high not to list the wastes. We solicit believe that these materials present levels, in some cases exceeding the TC comments on the proposed listing significant risk. level (5.0 mg/L) in TCLP leachate decisions described below. The North Carolina facility also samples. These wastes are coded as (1) North Carolina Facility. produces for sale sodium sulfate hazardous (D007). Both facilities treat (a) Residuals Commingled in Spent ‘‘saltcake’’ and purified sodium sulfate some of their D007 wastes on-site and Ore Residue Treatment Unit. The North anhydrous from the sodium dichromate send other D007 wastes off-site for Carolina facility commingles and treats production process. The Texas facility treatment and disposal at permitted several characteristic wastes from sells hydroxide solution from their Subtitle C hazardous waste facilities. sodium dichromate manufacturing in an sodium dichromate production process. Various other wastes which fall below on-site, tank-based treatment unit at the We found no information indicating that D007 regulatory levels are either treated North Carolina facility. These four the facilities which purchase these on-site or sent off-site for disposal. No sodium dichromate manufacturing materials burn them for energy recovery other constituents of concern were wastes are: or incorporate them into products that reported to be present in the wastes at —Waste heat boiler washout, which are are used on the land (use constituting levels of concern. accumulated solids from the internal

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components of the roasting kiln waste intact structures with minimal potential We found the treatment residues from heat boilers (Bevill exempt after for releases to groundwater. We do not saltcake drier scrubber solution to pose treatment) anticipate significant air releases no significant risks to groundwater. —Spent post-leach ore residue (Bevill because the wastes do not contain After treatment for hexavalent exempt after treatment) volatile constituents and have high chromium, the commingled reduced —Spent post-neutralization ore residue moisture content. Also, some of the chromium treatment residues from 1998 (Bevill exempt after treatment) tanks have covers which further reduce showed weekly TCLP analysis levels of —Saltcake drier scrubber wastewater the possibility of air releases. We are leachable chromium in the range of We consider the saltcake drier proposing not to list any of these four 0.01–1.00 mg/L for composite samples scrubber wastewater to be a wastestream wastestreams undergoing treatment in and <0.01–0.76 mg/L for grab samples. associated with the production of this tank system. Assuming that the saltcake drier sodium sulfate at the North Carolina (b) Residuals Disposed of On-Site. (i) scrubber wastewater’s percent facility, rather than a sodium Commingled reduced chromium contribution to total chromium in the dichromate manufacturing waste. treatment residues. The reduced commingled residues is equal to its Nevertheless, we chose to exercise our chromium sludge from the on-site spent percent contribution to total chromium discretion to evaluate the risk posed by ore residue treatment unit is slurried leaching from the commingled residues the treated and untreated form of this and conveyed directly from the (0.001%), the saltcake scrubber solution residue. As explained below, we did not treatment unit to one of two on-site was responsible for TCLP leaching × ¥7 × ¥5 find risks warranting listing. industrial Subtitle D disposal units levels of 1 10 to 1 10 mg/L for × ¥7 All four wastes catalogued above go (former limestone quarries). Of the composite samples and <3 10 to × ¥5 directly from their points of generation several treatment residues contributing 2.28 10 mg/L for grab samples. The to the on-site spent ore residue to the final commingled treatment HBL for ingestion of hexavalent treatment unit without intervening residue, only one falls within the scope chromium is 0.047 mg/L and 23 mg/L storage. The facility treats non-contact of today’s listing proposal; residue from for trivalent chromium. The AWQC for cooling tower blowdown, remediation treatment of saltcake drier scrubber hexavalent chromium is 0.011 mg/L and well water, and stormwater in the wastewater (we believe this is not 0.74 mg/L for trivalent chromium. Even at a maximum leaching level of 1×10¥5 treatment unit as well. The four within scope of the consent decree but mg/L, the leachable chromium manufacturing wastes comprise are evaluating it in this rule making). contribution of the saltcake drier approximately 60–65% by volume of Residues from the treatment of waste scrubber wastewater indicates a very the wastes entering the treatment unit. heat boiler washout, spent post-leach low level of risk to groundwater. The entire treatment process takes place ore residue, and spent post- neutralization ore residue are Bevill The treated wastes are disposed in an in a series of tanks with secondary uncovered disposal unit that resembles exempt mineral processing wastes containment. Treatment consists of a surface impoundment. However, given beyond the scope of today’s listing conversion of hexavalent chromium in the inorganic, nonvolatile nature of the proposal (see Section III.F.12(c)). the wastes to trivalent chromium with treated wastes, we do not believe they Stormwater and remediation well water pickle liquor (ferrous chloride reducing pose a risk through airborne pathways. are contaminated media whose agent). Trivalent chromium is a Given the low level of chromium treatment residues we also consider to generally less toxic and less soluble leaching attributable to the one be beyond the scope of the consent form of chromium. Wastes containing a treatment residue within the scope of decree (see section III.B of today’s high percentage of solids (waste heat today’s listing proposal and the lack of proposal). Therefore, we do not consider boiler washout, spent post-leach ore volatile constituents of concern, we residue, and spent post-neutralization the risks posed by these treatment propose not to list residues deriving ore residue) are also neutralized with residues. from the treatment of saltcake drier lime slurry in order to increase According to information the facility scrubber wastewater. precipitation of trivalent chromium submitted in their RCRA Section 3007 (ii) Commingled treated wastewaters. compounds out of solution. Survey response, the only potential The spent ore residue treatment unit The treatment sludge is then constituent of concern in the untreated described in the sections above has thickened in a series of clarifier tanks. saltcake drier scrubber wastewater is clarifier units which discharge a Limestone is added to the thickened chromium, detected at a level of 6 mg/ wastewater stream to tank-based sand sludge to further stabilize chromium L. Therefore, chromium is the only filters. After passing through sand and other metals. All of the tanks in the constituent we considered when filters, the treated wastewaters discharge treatment train have secondary assessing the level of risk from saltcake through an NPDES-permitted outfall. containment and some are covered. drier scrubber wastewater treatment These wastewaters are a mixture of non- Treated wastewaters, after passing residues. Bevill exempt and Bevill exempt through sand filters, discharge from the Of the total mass of chromium found treatment residues, and other treatment treatment unit under an NPDES permit in the commingled reduced chromium residues beyond the scope of the or travel with the treated solid residues treatment residues, the saltcake drier consent decree. The solids suspended in to the on-site industrial Subtitle D scrubber wastewater contributes the wastewaters are a mixture of Bevill disposal unit (see section approximately 0.001%. This estimate is exempt and non-Bevill exempt III.F.12.e(1)(b)ii below regarding the based on calculations using information treatment residues. The liquid portion, commingled treated wastewaters). the North Carolina facility provided to the majority of this wastestream, is a The Bevill exemption applies to the us on chromium contents and tonnages mixture of non-Bevill exempt residues, waste heat boiler washout, spent post- of waste exiting the spent ore residue some of which are within the scope of leach ore residue, and spent post- treatment unit. Both the information this listing determination, and some of neutralization ore residue only after the and the calculations are further detailed which derive from treatment of wastes are treated. We evaluated the in the ‘‘Sodium Dichromate Listing contaminated media and are therefore potential for releases from the treatment Background Document for the Inorganic not with the scope of this listing tanks. We assumed that the tanks were Chemical Listing Determination.’’ determination. We did not find any

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00060 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules 55743 significant potential for releases from also permitted to discharge 2.72 pounds within the scope of today’s listing the tanks. (We assess spent filter media of combined hexavalent and trivalent proposal. All other wastes are either from the sand filters separately in chromium per day. Making the Bevill exempt wastes or treatment section III.F.12.e(1)(c)ii below.) We conservative assumption that all 2.72 residues from contaminated media or concluded that the NPDES discharge is pounds of chromium are trivalent non-contact cooling water, none of exempt from RCRA regulation. chromium and given the amount of which falls within the scope of the A portion of the commingled treated treated wastewater discharged in 1998, consent decree. wastewaters remains with the we estimated that the facility produced As discussed in section commingled reduced chromium an NPDES effluent with an average III.F.12.e(1)(b), the saltcake drier treatment residues discharged for chromium concentration of 0.49 mg/L, scrubber solution contributes disposal to the facility’s on-site which is less than 23 mg/L, the HBL for approximately 0.001% of the total industrial Subtitle D disposal units. The trivalent chromium. Actual reported chromium exiting the spent ore residue facility also adds water to this mixture levels of total chromium release were treatment unit. Assuming that a waste’s from either the nearby Northeast Cape well below the permit limit. percent contribution to total chromium Fear River or the quarry in order to help Given that the levels of chromium exiting the treatment unit is equal to its slurry and convey the residues to the present in the on-site disposal unit percent contribution to total chromium disposal units. liquids are less than or within a factor leaching from waste exiting the unit, the The liquids which separate from the of two of the HBLs, we do not believe figures above indicate a TCLP leaching settled treatment residues in the they pose a risk to human health or the level of 2×10¥6 mg/L due to the facility’s disposal units are not Bevill environment through groundwater contributions of the saltcake drier exempt wastes (see Section III.F.12.c). underlying the disposal unit that scrubber wastewater. Because these liquids derive from the supports listing these wastewaters as a The HBL for hexavalent chromium is same treatment unit from which the hazardous waste. NPDES-discharged wastewaters (c) Residuals Disposed of Off-Site. (i) 0.047 mg/L and 23 mg/L for trivalent discussed above derive, we are Chromium-contaminated filters, chromium. The AWQC for hexavalent assuming their chemical composition is membranes, and other plant wastes. chromium is 0.011 mg/L and 0.74 mg/ very similar to that of the wastewaters This waste category from the North L for trivalent chromium. At a level of × ¥6 discharged under the facility’s NPDES Carolina facility includes spent filters, 2 10 mg/L, the leachable chromium permit. We used NPDES permit membranes, and various other plant contribution of the saltcake drier discharge data, available to the public wastes which exceed the TC level for scrubber wastewater presents a very low from the EPA’s Envirofacts database, 42 chromium. The wastes are stored in a level of risk. as a surrogate for characterization of this closed roll-off bin on-site before being The waste is inorganic in nature and wastewater (see discussion of SPLP sent off-site to a permitted Subtitle C therefore we do not expect it to contain filtrate in Section III.E.3). The exposure facility for treatment and disposal in a volatile constituents of concern. In pathway of concern is the groundwater landfill. We feel that applicable Subtitle addition, the waste is stored before underlying the facility’s disposal units C regulations adequately prevent disposal in a closed container. We do and consumption of the groundwater as mismanagement and therefore propose not believe, therefore, that this waste drinking water. not to list these wastes. poses a risk via airborne pathways. According to the North Carolina (ii) Spent sand filter sands. The North Given the low level of risk posed by the facility’s NPDES permit, the facility is Carolina facility generates waste sand saltcake drier scrubber wastewater allowed to discharge 0.31 pounds per material from the spent ore residue treatment residue contribution to day of hexavalent chromium to the treatment unit sand filters which filter leachable chromium levels in the spent Northeast Cape Fear River. Given the treated wastewaters prior to their sand filters and its nonvolatile nature, amount of treated wastewater reported NPDES-permitted discharge. The we propose not to list this waste. to be discharged in 1998 and using the purpose of the sand filters is to remove (2) Texas Facility. (a) Residuals permit loading as an upperbound value, any residual solids which the treatment Commingled in On-Site Treatment we estimate that the facility produced unit clarifiers fail to remove upstream in Units. At the Texas facility, an NPDES effluent with an average the treatment process. Since the commingling and treatment of four hexavalent chromium concentration of clarifiers capture the majority of the untreated wastes takes place in two 0.056 mg/L. This concentration is less solids, the sand filters capture smaller different on-site, tank-based treatment than twice the HBL for hexavalent amounts of treatment residue. The most units. The treatment residues from the chromium (0.047 mg/L).43 However, recent disposal of sand from the filters two treatment units are then co- according to NPDES compliance took place in 1997. The facility stores disposed in an on-site, Subtitle D monitoring data for the facility, no the spent sand in closed drums or roll- treatment surface impoundment. The hexavalent chromium was detected in off bins on-site before disposing of them first treatment unit, the spent ore the facility’s NPDES effluent in 1998. in an off-site industrial Subtitle D solid residue treatment unit, treats the Therefore, it is likely that the actual waste landfill. following two sodium dichromate concentration of hexavalent chromium According to information submitted manufacturing wastestreams: in the facility’s commingled treated to EPA by the North Carolina facility, wastewaters is less than the this residue does not exhibit any —spent post-neutralization ore residue concentration the facility is permitted to constituent above the TC level (Bevill exempt after treatment) release. according to TCLP leachate analysis. —caustic filter sludge from filtration of According to the North Carolina The only detected constituent of sodium hydroxide facility’s NPDES permit, the facility is potential concern was chromium, at a We consider caustic filter sludge to be level of 0.2 mg/L. Residue from a wastestream associated with the 42 http://www.epa.gov/enviro/index_java.html. treatment of saltcake drier scrubber production of sodium hydroxide rather 43 As described in Section III.E.3, we used wastewater is the only residue than a sodium dichromate engineering judgment to screen out constituents with concentrations within a factor of two of the contributing to the chromium levels in manufacturing waste. Nevertheless, we HBL. the spent sand filters which also falls chose to exercise our discretion to

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00061 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55744 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules evaluate the risk posed by the treated disposed of in the Subtitle D surface from the spent ore residue treatment and untreated forms of this residue. impoundment at the Texas facility, only unit analyzed with a facility-modified The spent ore residue treatment unit three fall within the scope of today’s version of the TCLP ranged between treatment tanks have both secondary listing proposal: residue from treatment 0.16 and 1.75 mg/L chromium (see containment and covers. Treatment of caustic filter sludge, residue from ‘‘Sodium Dichromate Listing consists of converting the hexavalent treatment of sodium chromate Background Document for the Inorganic chromium in the units to trivalent evaporation unit wastewaters, and Chemical Listing Determination’’ for chromium. Trivalent chromium is residue from treatment of sodium details). Therefore, conservatively typically a less soluble and less toxic dichromate evaporation unit assuming a maximum TCLP chromium form of chromium. Ore residue wastes wastewaters. Residues from the leaching level of 4.9 mg/L and assuming are not Bevill exempt and therefore treatment of post-neutralization spent that the percent contribution by the beyond the scope of the consent decree ore residue are Bevill exempt mineral three wastes to total chromium entering until treatment occurs. Therefore, we processing wastes beyond the scope of the treatment units is equal to their have evaluated the potential for releases today’s listing proposal (see section percent contribution to total chromium from these treatment tanks. We assume III.F.12.c). Stormwater and remediation leaching from treatment residues exiting the tanks are intact structures with well water are contaminated media the treatment units, the caustic filter minimal potential for releases to whose treatment residues we also sludge, sodium chromate evaporation groundwater. We believe the covers on consider to be beyond the scope of the unit wastewaters, and sodium the tanks reduce the potential for air consent decree (see section III.B). dichromate evaporation unit releases. Also, the wastes do not contain Therefore, we do not consider the risks wastewaters were responsible for TCLP volatile constituents. posed by these residues. chromium leaching levels of 2.45×10±6 The second treatment unit, the According to information the facility mg/L. wastewater treatment unit, treats the submitted in their RCRA Section 3007 The HBL for hexavalent chromium is following two sodium dichromate Survey response, the only potential 0.047 mg/L and 23 mg/L for trivalent manufacturing wastestreams: constituent of concern in the untreated chromium. The AWQC for hexavalent —sodium chromate evaporation unit sodium dichromate evaporation unit chromium is 0.011 mg/L and 0.74 mg/ wastewaters wastewater, sodium dichromate L for trivalent chromium. At a leaching —sodium dichromate evaporation unit evaporation unit wastewaters, and the level of 2.45×10±6 mg/L, the leachable wastewaters caustic filter sludge is chromium, chromium contribution of the caustic measured at a level of 0.5 mg/L, 0.5 mg/ The wastewater treatment unit also filter sludge, sodium chromate L and 20 mg/kg, respectively. Therefore, evaporation unit wastewaters, and the treats remediation well water and chromium is the only constituent we sodium dichromate evaporation unit stormwater, two types of contaminated considered when assessing the level of wastewaters indicates a very low level media which are outside the scope of risk from sodium dichromate of risk to groundwater from potential the consent decree. The two evaporation unit wastewater, sodium releases from the surface impoundment. wastewaters within the scope of the chromate evaporation unit wastewater, consent decree make up approximately and caustic filter sludge treatment The waste is metallic and inorganic in 9% of the total volume of the wastes residues. nature and therefore we do not expect entering the treatment unit. The facility Of the total chromium contributed to it to contain volatile constituents of converts hexavalent chromium to less the co-disposed reduced chromium concern. We do not believe, therefore, toxic trivalent chromium during this treatment residue by all incoming that this waste poses a risk via airborne treatment process. The tanks do not wastes, the sodium dichromate pathways. Given the low level of have covers. evaporation unit wastewater, sodium chromium leachate deriving from the We evaluated the tanks for potential chromate evaporation unit wastewater, three treatment residues within the releases to the environment. We and the caustic filter sludge contribute scope of today’s listing proposal and assumed the tank structures were intact 5×10±5 percent by weight. This estimate placed into the surface impoundments, and therefore posed minimal potential is based on calculations using we propose not to list residues deriving for releases to groundwater. Since the information the Texas facility provided from the treatment of caustic filter wastewaters contain no volatile to us on chromium contents and sludge, sodium chromate evaporation constituents, we found no significant tonnages of wastes entering the spent unit wastewater, and sodium potential for air releases. We are ore residue treatment unit and the dichromate evaporation unit proposing not to list the wastes in these wastewater treatment unit on-site. Both wastewater. treatment tanks. the information and the calculations are (ii) Commingled treated wastewaters. The facility disposes the treatment described further in the ‘‘Sodium Treated wastewaters commingled with materials from the two tank systems Dichromate Listing Background the commingled reduced chromium described above in an on-site surface Document for the Inorganic Chemical treatment residues separate from these impoundment. We describe that surface Listing Determination.’’ solid residues in the Texas facility’s impoundment in the next section. The facility did not provide us with surface impoundment disposal unit. (b) Residuals Disposed of On-Site. (i) TCLP, SPLP, or total constituent These liquids are not Bevill exempt Commingled reduced chromium analyses for the co-disposed reduced wastes (see Section III.F.12.3). The treatment residues. The treatment chromium treatment residues. However, solids suspended in the wastewaters are residues from the two treatment tank the facility did report to us that reduced a mixture of Bevill exempt and non- systems described in the section above chromium treatment residues do not Bevill exempt treatment residues. The are piped directly to the facility’s on- exceed the TC level of 5.0 mg/L liquid portion, the majority of this site, double-lined, Subtitle D surface according to TCLP analysis. In addition, wastestream, is a mixture of non-Bevill impoundment for co-disposal and the facility reported that for the time exempt residues, some of which are dewatering. Of the several treatment period between October 1, 1998 and within the scope of this listing residues contributing to the mass of December 31, 1998, weekly samples of determination, and some of which reduced chromium treatment residue reduced chromium treatment residues derive from treatment of contaminated

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The Texas facility reports in maximum TCLP chromium leaching (see discussion below in Section their RCRA Section 3007 Survey level of 4.9 mg/L, and assuming that the III.F.12.e(2)(c)(ii). We therefore assume response that process filters and percent contribution to total chromium that the chemical composition of the membranes and baghouse bags from by the three wastes entering the treated wastewaters in the surface their facility exceed the TC level for treatment units is equal to their percent impoundment is very similar to that of chromium and are coded D007. The contribution to total chromium leaching the NPDES permitted discharge. We facility also reports that they produce from treatment residues exiting the used NPDES permit discharge data, empty containers and other plant wastes treatment units, the caustic filter sludge, available to the public from the EPA’s contaminated with chromium which are sodium chromate evaporation Envirofacts database,44 as a surrogate for also coded D007. The facility stores wastewaters, and sodium dichromate characterization of this wastewater (see these hazardous wastes in a closed evaporation unit wastewaters were discussion of SPLP filtrate in Section rolloff bin on-site before sending them responsible for TCLP chromium III.E.3). The exposure pathway of off-site to a permitted Subtitle C leaching levels of 2.4×10±6 mg/L. concern is the groundwater underlying hazardous waste facility for treatment The HBL for hexavalent chromium is the facility’s disposal units and and landfill disposal. These wastes are 0.047 mg/L and 23 mg/L for trivalent consumption of the groundwater as sufficiently managed under current chromium. The AWQC for hexavalent drinking water. RCRA Subtitle C regulations and chromium is 0.011 mg/L and 0.74 mg/ According to the Texas facility’s 1998 therefore we propose not to list these L for trivalent chromium. At a level of NPDES monitoring data, the facility wastes. 2.4×10±6 mg/L, the leachable chromium discharged an average of 0.018 pounds (ii) Spent sand filter sands. The Texas contribution of the sodium dichromate of hexavalent chromium each day facility generates waste sand material evaporation unit wastewater, the through their internal NPDES outfall. from the sand filters which filter treated sodium chromate evaporation Given the amount of treated wastewater wastewaters prior to their NPDES wastewaters, and the caustic filter the facility reported as discharge from permitted discharge from the facility’s sludge presents a very low level of risk. the surface impoundment in 1998, we on-site surface impoundment. The The waste is metallic and inorganic in estimate that the facility produced an purpose of the sand filters is to remove nature, and therefore we do not expect NPDES effluent with an average any residual solids which fail to settle it to contain volatile constituents of hexavalent chromium concentration of in the surface impoundment. Since the concern. We do not believe, therefore, 0.016 mg/L. This concentration is less majority of the solids settle in the that this waste poses a risk via airborne than the HBL for hexavalent chromium surface impoundment, the sand filters pathways. Given the low level of risk (0.047 mg/L). captures smaller amounts of reduced posed by the contribution of According to the Texas facility’s chromium treatment residue. constituents in the spent filter sands NPDES monitoring data for 1998, the Approximately 2 MT of spent sand filter attributable to caustic filter sludge, facility released an average of 0.46 sand is disposed of every two years. The sodium chromate evaporation unit pounds of combined hexavalent and facility stores the spent sand in non- wastewaters, and sodium dichromate trivalent chromium per day. Making the hazardous soil bins on-site before evaporation unit wastewater treatment conservative assumption that all 0.46 disposing of it at an off-site Subtitle D residue, the absence of volatile pounds of chromium are trivalent industrial landfill. constituents of concern, and the chromium and given the amount of According to the Texas facility, this relatively small volume of the total treated wastewater discharged in 1998, residue does not exhibit any constituent waste, we propose not to list this waste. we estimated that the facility produced above the TC level according to TCLP an NPDES effluent with an average leachate analysis. Residues from 13. Sodium Phosphate From Wet chromium concentration of 0.41 mg/L, treatment of caustic filter sludge, Process Phosphoric Acid which is less than 23 mg/L, the HBL for sodium chromate evaporation unit a. Summary. We propose not to list trivalent chromium. wastewaters, and sodium dichromate any wastes from the production of Wastes in the surface impoundment evaporation unit wastewaters are the sodium phosphate from wet process dewater and the resulting wastewaters only residues contributing to the phosphoric acid as hazardous under pass out of the surface impoundment potential constituent of concern levels subtitle C of RCRA. Many of these and through tank-based sand filters. in the spent sand filters which also fall secondary materials are piped back into From the sand filters, the treated within the scope of today’s listing the production process; other wastes are wastewaters then discharge through an proposal. All other wastes are either discharged to a permitted publicly- NPDES-permitted outfall. These Bevill exempt wastes or treatment owned treatment works (POTW). Other wastewaters are a mixture of non-Bevill residues from contaminated media, materials are sent to Subtitle D exempt and Bevill exempt treatment neither of which falls within the scope industrial landfills. After an analysis of residues, and other treatment residues of the consent decree. waste management practices and beyond the scope of the consent decree. Chromium was the only potential potential exposure pathways, we We did not find any significant constituent of concern detected in the conclude that there are no risk pathways potential for releases from the sand filter sodium chromate evaporation unit of concern. These wastes do not meet tanks. (We assess spent filter media wastewaters, sodium dichromate the criteria set out at 40 CFR from the sand filters separately in evaporation unit wastewaters and the 261.11(a)(3) for listing as hazardous. Section III.F.12.e(2)(c)(ii) We concluded caustic filter sludge, and is therefore the b. Description of the sodium only potential constituent of concern we phosphate industry. Sodium phosphate 44 http://www.epa.gov/enviro/index_java.html considered in the spent sand filter is the more general chemical name for

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00063 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55746 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules a wide variety of salts produced from The processes for monosodium process pass through dryers. The the neutralization of phosphoric acid. dihydrogen phosphate, disodium finished product is packaged or shipped Some of the salts produced by the monohydrogen phosphate, and in bulk. facilities in this industry are trisodium phosphate are similar except Sodium hexametaphosphate and monosodium dihydrogen phosphate for the ratio of phosphoric acid to soda sodium tripolyphosphate are also (H2NaPO4), disodium monohydrogen ash at the reactor stage and the type, produced from food-grade phosphoric phosphate (HNa2PO4), trisodium size and construction of the crystallizing acid and soda ash. Both processes start phosphate (Na3PO4), sodium and drying equipment. The raw with a reaction between phosphoric hexametaphosphate (Na4P 4O12), and materials are water, phosphoric acid, acid and soda ash. For the sodium sodium tripolyphosphate (Na5P3O10). soda ash, and caustic. The purified hexametaphosphate process, the The various phosphate salts produced phosphoric acid is manufactured product is fed to a furnace which melts are used for a wide variety of purposes, elsewhere through the wet-acid the mix and converts it to sodium ranging from a water soluble solid acid purification method and is food grade. hexametaphosphate. For the sodium and pH buffer for acidic cleaners to The process starts with a reaction tripolyphosphate process, the reaction products manufactured for the food between phosphoric acid, soda ash, and discharge is dried and heat treated in a industry 45. Sodium phosphate is caustic. The solution is used to make converter to convert it to sodium produced from wet process phosphoric the monosodium dihydrogen phosphate, tripolyphosphate. In both processes, the acid by two manufacturing companies at which passes through a polishing filter product is cooled, sized, stored, and four locations in the United States. For before shipment to customers. The packaged for shipment. more detailed information concerning sodium to phosphorus ratio of the c. What kinds of wastes are generated this industry, see ‘‘Sodium Phosphate solution is adjusted with caustic to by these processes? A brief description Listing Background Document for the make disodium monohydrogen of the waste categories, how they are Inorganic Chemical Listing phosphate and trisodium phosphate. generated, their volumes across the Determination’’ in the docket for today’s These solutions are filtered and then industry, and how they are managed is proposal. crystallized. The crystals from each presented in Table III–34:

TABLE III±34.ÐSODIUM PHOSPHATE PRODUCTION WASTES

1998 Volume Waste category (MT) Source Management practices

Filter press cakes ...... 120 ...... Product polishing ...... Recycled or Subtitle D landfill. Mix area filters ...... 0.009 ...... Product polishing ...... Subtitle D landfill. Dust collector filter bags ...... 2.1 ...... Drying and grinding processes ...... Subtitle D landfill. Scrubber waters and effluents ...... 32 ...... Process vapor scrubbers ...... POTW or recycled. Product dust collected ...... Not reported ..... Drying and grinding processes ...... Recycled or Subtitle D landfill. Off-specification product...... 771 ...... Off-specification grinding or customer Recycled or Subtitle D landfill. returns.

For those scenarios where secondary into the process from where it How Was This Waste Characterized? materials (filter press cakes, product originated, is not a solid waste. For dust, off-specification product, and those scenarios where wastes are We collected two samples of this scrubber water) are piped back to the discharged via the facility’s common residual at one facility. Based on our production process, we could identify sewage line to permitted publicly- assessment of the raw materials and no potential route for significant owned treatment works (POTWs), these production processes used across the exposure prior to reuse. In addition, we wastes are excluded from RCRA (40 CFR industry, we believe these samples are evaluated all wastes generated after 261.4(a)(1)(ii)). For those scenarios representative of the range of waste reinsertion of these materials into the where wastes are sent to industrial characteristics at the other three sodium process and we do not believe that these subtitle D landfills, we performed a risk phosphate production facilities. assessment to help us determine secondary materials present significant Constituents detected above their HBLs whether these risks warranted listing. are summarized in Table III–35. threats. Also, off-specification product, d. Agency evaluation. (1) Filter press when reinserted without reclamation cake and mix area filters.

TABLE III±35.ÐCHARACTERIZATION OF FILTER PRESS CAKES FROM SODIUM PHOSPHATE PRODUCTION

Total TCLP SPLP HBL Parameter (mg/kg) (mg/l) (mg/l) (mg/l)

Primary filter press cake (Sample RCH±1±SP±01): Antimony ...... 0.5 <0.5 0.0298 0.006 Thallium ...... <2 <2 0.0055 0.001

45 In this preamble, we often refer to sodium safe’’ (GRAS). The FDA states that: ‘‘This substance considers the composition and properties of the phosphate produced for the food industry as ‘‘food is generally recognized as safe when used as in substance, the amount likely to be consumed, its grade.’’ The Food and Drug Administration (FDA), accordance with good manufacturing practice.’’ probable long-term effects and various safety Department of Health and Human Services, refers (See, for example, 21 CFR 182.1778, 182.6290, factors. to the various sodium phosphates used in the food 182.6778, and 182.8778.) In deciding whether a industry as ‘‘substances generally recognized as food additive should be approved, the FDA

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TABLE III±35.ÐCHARACTERIZATION OF FILTER PRESS CAKES FROM SODIUM PHOSPHATE PRODUCTIONÐContinued

Total TCLP SPLP HBL Parameter (mg/kg) (mg/l) (mg/l) (mg/l)

Tray filter cake (Sample RCH±1±SP±02): Antimony ...... <0.5 <0.5 <0.025 0.006 Thallium ...... <2 <2 0.0079 0.001

What Management Scenarios Were Chemical Manufacturing Wastes’’ in the concern. For a more complete Assessed and How Was the Risk docket for this proposed rulemaking. description of this analysis, see ‘‘Risk Assessment Established? Assessment for the Listing These wastes go to industrial subtitle TABLE III±36.ÐPROBABILISTIC RISK Determinations for Inorganic Chemical D landfills and we therefore determined RESULTS FOR FILTER PRESS CAKES Manufacturing Wastes’’ in the docket for that we would model the scenario of off- this proposed rulemaking. site disposal in an industrial D landfill. Antimony Thallium The detected SPLP levels for antimony did not screen out using the We assessed the off-site landfill scenario Percentile Adult Child Adult Child using the hydrogeologic properties HQ HQ HQ HQ de minimis volume analysis. We associated with the geographic areas conducted full groundwater modeling where the landfills reported in the Industrial for the industrial landfill scenario for survey are located. landfill: this constituent. We assessed the off-site We gave the SPLP results primary 90th ...... 0.001 0.003 0.002 0.003 landfill scenario using the probabilistic consideration as there is no reported 95th ...... 0.004 0.008 0.004 0.008 approach for off-site landfills described management in municipal landfills in section III.E. (2) Dust collector filter bags. (where the TCLP results would be What Is EPA’s Listing Rationale for This relevant). Based on the sampling results How Was This Waste Characterized? Waste? summarized above, we decided that We collected one sample of this modeling was necessary for two From the results of the risk residual. Based on our assessment of the constituents of concern: antimony and assessment, summarized below in Table raw materials and production processes thallium. For antimony, we used one- III–38, antimony (the constituent of used across the industry, we believe this half of the detection limit as a model concern) does not pose a substantial sample is representative of similar input for sample RCH–1–SP–02. We present or potential hazard to human wastes at the other three sodium used the probabilistic approach for an health and the environment. The hazard phosphate production facilities. The off-site industrial Subtitle D landfill quotients for antimony, for both the waste constituents detected at levels described in section III.E of today’s adult and child exposure scenarios, are above their HBLs are summarized in proposal. less than 0.007 at the 95th percentile. As Table III–37: a matter of policy, EPA generally does What Is EPA’s Listing Rationale for This not consider listing wastes with Waste? TABLE III±37.ÐCHARACTERIZATION OF predicted hazard quotients of less than From the results of the risk DUST COLLECTOR FILTER BAG 1.0. We see no special concerns assessment, summarized below in Table FROM SODIUM PHOSPHATE PRO- warranting an exception to this policy. III–36, neither antimony nor thallium DUCTION Therefore, we believe that this waste (the constituents of concern) pose a [Sample RCH±1±SP±03] does not warrant listing. For a more substantial present or potential hazard complete description of this analysis, to human health and the environment. see ‘‘Risk Assessment for the Listing Param- Total TCLP SPLP HBL The hazard quotients for both eter (mg/ (mg/l) (mg/l) (mg/l) Determinations for Inorganic Chemical constituents, for both the adult and kg) Manufacturing Wastes’’ in the docket for child exposure scenarios, are less than this proposed rulemaking. Antimony 48.8 <0.5 0.309 0.006 0.008 at the 95th percentile. As a matter Arsenic .. <0.5 <0.5 0.0064 0.0007 of policy, EPA generally does not TABLE III±38.ÐPROBABILISTIC RISK consider listing wastes with predicted What Management Scenarios Were RESULTS FOR DUST COLLECTOR BAGS hazard quotients of less than 1.0. We see Assessed and How Was the Risk no special concerns warranting an Antimony Assessment Established? exception to this policy. Therefore, we Percentile Industry reported that this waste is Adult Child believe that these wastes do not warrant HQ HQ listing. managed in off-site industrial D For the mix area filters, the location landfills. We assessed this scenario. Industrial landfill: of these filters indicates that any Antimony and arsenic are the 90th ...... 0.001 0.002 contaminants found would be similar to constituents of concern. 95th ...... 0.003 0.003 those of the filter press cake. Given that Because the volume of this waste is our evaluation of the much larger relatively small, we first used the de (3) Scrubber waters and effluents. We volume filter press cake yielded no minimis waste quantity screening did not evaluate scenarios where these significant risk, we are also proposing analysis (described in section III.E.3) to secondary materials are piped back into not to list the very small volume mix screen the potential risk to groundwater the production process because there is area filters. associated with landfilling this waste. no potential for exposure. For those For a more complete description of We found that the SPLP data for arsenic scenarios where wastes are managed in these analyses, see ‘‘Risk Assessment for screens out because the waste volume is a tank, the impervious nature of the the Listing Determinations for Inorganic insufficient to release arsenic at levels of construction materials (concrete,

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00065 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55748 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules fiberglass, or steel) of tanks are unlikely tetrachloride production exempt Sulfate Process. In the sulfate process, to result in releases to groundwater in under section 261.4(b)(7)] ilmenite ore or slag with high TiO2 all but the most catastrophic scenarios. We propose not to list the remainder content is digested with sulfuric acid, We also are not concerned with of the wastes generated by this sector. forming a porous cake; this cake is potential air releases from these tanks as We do not believe these wastes pose further dissolved by dilute acid to form neither volatile contaminants nor threats to human health or the titanyl sulfate (TiOSO4). Iron may be airborne particulates are likely to be environment that warrant listing. We added to the digestion process to ensure present in these aqueous wastes. For have not identified risks of concern that iron impurities remain in the ∂ those scenarios where wastes are associated with the current management ferrous (Fe2 ) state so that the eventual discharged via the facility’s common of these wastes that support a listing TiO2 product can be easily washed. The sewage line to POTWs, these wastes are determination. Our findings, however, titanyl sulfate solution is then clarified, excluded from RCRA (40 CFR do not change the applicability of yielding a waste sulfate digestion 261.4(a)(1)(ii)). Furthermore, these existing standards and regulations, such sludge, and then concentrated through discharges are regulated by the Clean as the hazardous waste characteristics, vacuum evaporation. The filtered titanyl Water Act pretreatment standards. They to these wastes and this industry. sulfate solution is vacuum-evaporated a do not warrant listing. We propose not b. Description of the titanium dioxide second time and hydrolyzed to to list this waste. industry. There are nine facilities precipitate hydrated titania (TiO(OH)2). (4) Product dust collected. All producing titanium dioxide. There are The titania hydrate is then filtered and collected dust that can be recycled is three distinct processes currently in use: washed, yielding filtrate waste and recycled back into the production the chloride process, the sulfate process, wastewater, respectively, before being ° process. Due to production constraints, and the chloride-ilmenite process. Six calcined at 1,000 C to produce the TiO2 some portion of this collected product facilities use the chloride process. Two product. dust cannot be recycled back to the of these six facilities also produce Chloride-Ilmenite Process. In the process and is instead sent to an titanium dioxide via the sulfate process. chloride-ilmenite process, ilmenite ore industrial Subtitle D landfill. However, Three separate facilities use only the is converted to titanium tetrachloride. this landfilled product is still food-grade chloride-ilmenite process. As in the chloride process, the chloride- product. Because this ‘‘waste’’ is, in fact, Chloride Process. In the chloride ilmenite process takes place in a food-grade product, we believe it process, rutile or high-grade ilmenite is chlorinator in which the ore is unlikely that it contains any constituent converted to titanium tetrachloride chlorinated in the presence of coke as a exceeding health-based limits based on (TiCl4). The conversion takes place in a reducing agent. Vent gases from the ingestion. Therefore, we propose not to chlorinator in the presence of chlorine chlorinator are scrubbed prior to venting list this waste. gas with petroleum coke added as a to the atmosphere. Non-volatile metal (5) Off-specification product. Much of reductant. All U.S. producers of TiCl4 chlorides and unreacted coke and ore this material is reused in the production use fluidized bed chlorinators. Vent solids are removed from the gaseous process with no potential for exposure. gases from the chlorinator are scrubbed product stream. The gaseous product However, because of production prior to venting to the atmosphere. Non- stream then is purified further to constraints, they cannot always work all volatile metal chlorides and unreacted separate the titanium tetrachloride from of this material back into the process, coke and ore solids are removed from other volatile metal chloride impurities, and it must be disposed in an industrial the gaseous product stream. The including ferric chloride (FeCl3) which subtitle D landfill. In all cases, product facilities also generate waste acid, is present in higher concentrations than is rejected by a customer because of which they mingle with coke and ore the chloride process due to the high iron physical property problems—i.e., solids before treatment. Vent gases from content in the ore. The separation is particle size—rather than chemical the chlorinator are scrubbed prior to done via condensation and chemical problems or contaminants. Because this venting to the atmosphere. The volatile treatment. The process for converting ‘‘waste’’ is, in fact, food-grade product, TiCl4 and other volatile metal the purified TiCl4 product stream to we believe it unlikely that it contains compounds such as vanadium TiO2 is similar to that used in the any constituent exceeding health-based oxychloride, exit the chlorinator as chloride process, as described above. limits based on ingestion. Therefore, we overhead vapor. The gaseous product c. What kind of wastes are generated propose not to list this waste. stream is purified to separate the by these processes?. The wastes generated by the titanium dioxide sector 14. Titanium Dioxide titanium tetrachloride from other metal chloride impurities using processes are described in overview below, a. Summary. We evaluated wastes such as partial condensation and organized by process. Additional detail from the production of titanium dioxide chemical treatment. Finally, vanadium on these wastes is provided in the and propose to list one waste and not compounds, which have boiling points background document for this sector. to list all of the others. Certain wastes close to that of TiCl4, are removed from The wastes generated by the chloride from titanium dioxide production are the titanium tetrachloride by process include: exempt mineral processing wastes and complexing with mineral oil and —Commingled wastewaters, including were not assessed as part of today’s reducing with hydrogen sulfide, or by process and non-process wastewaters listing determination because they are complexing with copper. The purified from chlorinator coke and ore solids outside the scope of the consent decree. TiCl4 is then oxidized to TiO2, driving recovery, reaction and chemical tank We are proposing to list nonwastewaters off chlorine gas, which is recycled to the storage scrubbers, product finishing from the chloride ilmenite process chlorinator. The pure TiO2 is slurried operations, wastewater treatment and (unless otherwise exempted). and sent to the finishing process which chlorinator solids decantation, and K178 Nonwastewaters from the includes milling, addition of inorganic on-site landfill leachate. production of titanium dioxide by the and organic surface treatments, and/or —Chloride process waste solids from chloride-ilmenite process. (T) [This spray drying of the product TiO2. The titanium tetrachloride production listing does not apply to chloride product can be sold as a packaged dry (exempt as mineral processing wastes, process waste solids from titanium solid or a water-based slurry. see 40 CFR 261.4(b)(7)).

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—Wastewater treatment sludges with wastewaters from the chloride oxidation unit tank and equipment generated by facilities that have process. vents, supernatant or filtrate from chloride-only processes (exempt —Wastewater treatment sludges. These coke and ore solids management and mineral processing wastes at those wastewater treatment sludges are wastewater treatment disposal facilities with no contribution of generated from commingled chloride impoundments. The wastewaters are solids from oxidation and finishing) process and sulfate process commingled prior to being introduced —Waste sands from finishing (milling) wastewaters by facilities that have into the wastewater treatment system. of the titanium dioxide product and both processes. The wastewater —Other spent scrubber waters from the scouring of oxidation process units. treatment consists of elementary reaction fume disposal system. The —Vanadium wastes generated in the neutralization and precipitation or wastewaters are pretreated and are purification process. filtration. subsequently commingled with other The wastes generated by the sulfate —Acids from intermediate titanium wastewaters prior to being introduced process (used at two plants that also use product filtration/bleaching units and to the wastewater treatment system. the chloride process) include: product calciner overhead scrubbers. —Non-exempt non-wastewaters, —Primary and secondary gypsum, —Product milling sand from finishing including the portion of wastewater which is produced when the waste operations. treatment solids derived from the sulfuric acid generated from the The wastes generated by the chloride- neutralization of process and non- filtering of titanium dioxide hydrate ilmenite process include: process wastewaters from oxidation solution is neutralized with calcium —Coke and ore solids (exempt as and finishing, and solids from ferric carbonate. mineral processing wastes, see 40 CFR chloride filtration. —Digestion sludge from the clarification 261.4(b)(7)) that are not consumed by —HCl from the reaction scrubber. of the titanyl sulfate liquor that is the chlorination process. These solids —Additive feeder vent filter solids produced during the acid digester are conveyed through the process as generated in the oxidation process. step. part of various wastestreams. —Vanadium waste generated in the —Wastewaters from the sulfuric acid —Waste acid (metal chloride) solution, purification process. digestion scrubber which removes usually called ferric or iron chloride, —Off-specification titanium dioxide acidic components and entrained that is separated from the gaseous product. solids from reaction gases, evaporator titanium tetrachloride product stream condensate from the precipitation and acidified. —Rail car product washout wastewater. unit, the calciner scrubber, the sulfate —Process and non-process wastewaters —Waste sand removed from a reactor waste sludge settling pond from reaction and oxidation purge stream (coke and ore solids) supernatant, and the primary and scrubbers, reactant and treatment Table III–39, below, summarizes our secondary gypsum precipitation units. chemical storage scrubbers, product information about the wastes generated These wastewaters are commingled finishing, HCl storage vent scrubber, rom the production of titanium dioxide.

TABLE III±39.ÐTITANIUM DIOXIDE WASTES

Number of 1998 Reported hazard Waste category generators volumes (MT) codes Management practices

Commingled chloride process wastewaters .. 4 7,614,358 ...... D002, D007 ...... Neutralization, solids settling, NPDES dis- charge. Chloride process solids (Bevill exempt) ...... 6 1,200,000 ...... none ...... On-site impoundments, on-site Subtitle D landfills. Waste sands from oxidation, milling and 3 9,485 ...... none ...... On-site industrial Subtitle D landfill; off-site scouring. industrial Subtitle D landfill. Gypsum from sulfate process ...... 2 46 69,500 ...... none ...... On-site waste pile storage; on-site industrial Subtitle D landfill; sold for various uses. Digestion scrubber water...... 2 2,000,333 ...... Neutralization in dedicated impoundment; commingled with other wastewaters. Digestion sludge from sulfate process ...... 2 41,494 ...... D002 ...... Unlined impoundment, dewatering, on-site industrial Subtitle D landfill. Commingled wastewaters from the chloride 2 16,184,031 ...... none ...... Neutralization, solids settling in unlined sur- and sulfate process. face impoundments, NPDES discharge. Wastewater treatment sludges from commin- 2 159,121 ...... none ...... Dewatering, on-site industrial Subtitle D gled chloride and sulfate process (partially landfill. Bevill exempt). Waste acid (ferric chloride) from chloride-il- 3 1,883,000 ...... D002, D007, On-site hazardous waste underground injec- menite process. D008. tion; reuse as raw material in sodium chloride production; storage in tanks and unlined impoundment prior to sale as water and wastewater treatment reagent. Chloride ilmenite process solids (Bevill ex- 3 not reported ...... none ...... On-site dewatering; on-site Subtitle D indus- empt). trial landfill; on-site unlined impoundment; various reuses. Non-exempt nonwastewaters from the chlo- 3 14,600 ...... none ...... On-site dewatering; on-site Subtitle D indus- ride-ilmenite process. trial landfill; on-site unlined impoundment; various reuses. HCl from reaction scrubber, chloride-ilmenite 3 not reported ...... D002 ...... On-site wastewater treatment, on-site reuse. process. Commingled wastewaters from the chloride- 3 13,556,000 ...... none ...... On-site neutralization, solids settling, ilmenite process. NPDES discharge.

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TABLE III±39.ÐTITANIUM DIOXIDE WASTESÐContinued

Number of 1998 Reported hazard Waste category generators volumes (MT) codes Management practices

Additive vent filter solids from chloride-ilmen- 1 < 1 ...... none ...... Off-site Subtitle D industrial landfill. ite process. Vanadium waste from the chloride-ilmenite 4 not reported ...... none ...... Returned to reaction area for TiCl 4 recov- and chloride process. ery, remaining vanadium wastes are in- corporated in solids streams. Off-spec titanium dioxide product ...... 2 563 ...... none ...... Off-site Subtitle D industrial landfill. Railcar/trailer product washout ...... 1 <10,000 ...... none ...... On-site storage in unlined surface impound- ment, on-site wastewater treatment. 46 Additional volumes are used as products.

The manufacturers also produce The industry reported a number of discussed these solids, we believe that materials that are reused in other wastes generated from the storage and they also fall within the exemption. processes that are outside the scope of handling of various raw materials which While they are removed from the the consent decree. With one exception are exempt because they are associated product stream and various other wastes described below, we did not evaluate with beneficiation. Solid wastes from at points other than where the majority these materials, or wastes generated the extraction/beneficiation of ores and of the solids are separated from the during co-product production for the minerals are Bevill exempt solid wastes TiCl4 gas stream, they are similarly purposes of today’s listing (see 51 FR 24496, July 3, 1986 and 54 composed of unreacted ore and coke determinations, because they were FR 36592, September 1, 1989). These solids from the chlorination reactor. outside the scope of the consent decree. wastes are described in the background They fit within the plain language of the One facility produces sulfur from the document for this sector. We have not exemption. assessed these wastes because they are treatment of off-gases. Because the off- Solids also are generated from the exempt under 40 CFR 261.4(b)(7). gas is produced from a production unit oxidation and finishing stages of The only relevant mineral processing rather than a waste management unit titanium dioxide production. These waste exemption consists of ‘‘chloride solids are non-exempt solid wastes (not and is conveyed to its destination via process waste solids from titanium piping, the gas is not a solid waste. covered by the exemption). Most tetrachloride production’’ (see 40 CFR titanium dioxide producers commingle RCRA Section 1004(27) excludes non- 261.4(b)(7)(ii)(S)). The consent decree contained gases from the definition of wastewaters from titanium tetrachloride mandating today’s proposal states in production with wastewaters from solid waste and thus they cannot be paragraph 1.g that Bevill exempt wastes considered a hazardous waste. (See 54 oxidation and finishing. To the extent are not within the scope of the consent that the resultant sludges contain non- FR 50973) Because this gas is not a solid decree as it applies to the inorganic waste when produced, we did not exempt solids, we have assessed that chemical listing determinations, and portion of those solids. evaluate it further for purposes of specifically that ‘‘chloride process waste listing. Due to process variations, each solids’’ need not be assessed within the facility using the chloride or chloride- d. What wastes from these processes titanium dioxide sector. Titanium ilmenite process generates its exempt are exempt mineral processing wastes? tetrachloride production occurs in both solids in slightly different ways. The In July of 1988, the U.S. Court of the chloride and chloride-ilmenite general principles that we used to 47 Appeals, for the D.C. Circuit in processes. determine the Bevill status of these Environmental Defense Fund v. EPA The chloride process waste solids are wastes include the following: (EDF II), 852 F.2d 1316 (D.C. Cir. 1988), generated during the chlorination cert. denied, 489 U.S. 1011(1989), reaction of the titanium ore in the —Extraction and beneficiation ends just ordered EPA to restrict the scope of the reducing presence of coke at elevated before chlorination occurs. Wastes temperatures, and are generated from generated prior to this point are Bevill Bevill mining waste exclusion, as it exempt, outside the scope of the consent applied to mineral processing wastes. In both the chloride process and the decree and therefore not addressed in this response, EPA promulgated rules on chloride-ilmenite process. The majority rulemaking. The chlorinator marks the September 1, 1989 (54 FR 36592) and on of these solids are removed from the beginning of mineral processing because January 23, 1990 (55 FR 2322), issued a reaction area as a mass and are the ore undergoes a physical/chemical Report to Congress on Wastes from quenched, neutralized, settled and change (see 54 FR 36619, September 1, Mineral Processing on July 31, 1990, disposed as exempt materials. 1989). 54 FR 36621 further notes, and published a regulatory Additional solids from the reactor are ‘‘Likewise, EPA considered titanium determination published on June 13, carried overhead with the TiCl4 product tetrachloride produced during the titanium gas stream and are subsequently chloride [sic] process to be a saleable 1991 (56 FR 27300). The list of Bevill product; any further processing subsequent exempt wastes is set out at 40 CFR removed in various scrubbing units. to its production is considered to be 261.4(b)(7). We relied on these Bevill Although EPA has not previously chemical manufacturing.’’ rulemakings to determine the Bevill —Mineral processing ends when titanium status of waste streams in the titanium 47 All sulfate process waste solids and liquids are dioxide is produced in the oxidation unit. dioxide sector. non-exempt mineral processing wastes (see 55 FR Further steps are chemical manufacturing. 2322, January 23, 1990). 55 FR 2392 noted that all The Agency defines the beginning of The production of titanium dioxide sulfate process waste solids and wastewaters from oxidation as the beginning of chemical results in the generation of 2 categories the production of titanium dioxide do not meet the high volume/low hazard criteria established in the manufacturing because the facility is using of exempt waste: beneficiation wastes September 1, 1989 Bevill rule and therefore were a saleable mineral product, titanium and exempt mineral processing wastes. not eligible for continued coverage under the Bevill tetrachloride, to produce titanium dioxide These categories are described below. exclusion (see 54 FR 36592). (see 54 FR 366211).

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—The mineral processing exemption only presence of coke, and in fact we found risk assessment to fully evaluate the covers solids from the production of measurable levels of these compounds potential for risks. See section titanium tetrachloride. These solids, in wastes from the chloride and III.F.14.e(10) below. therefore, are outside of the consent decree. chloride-ilmenite processes. These data At least six streams of solid-bearing 5. Agency Evaluation material leave the chlorination reaction are presented in the Titanium Dioxide area. The status of these streams is as Listing Background Document and (1) Commingled wastewaters from the follows: associated analytical data reports in the chloride process, including wastewaters (1) Titanium tetrachloride going on for docket for today’s notice. As explained from coke and ore recovery, scrubber further production. All wastes formed during in this background document, we water, finishing wastewaters and sludge further processing of this gaseous product believe that these compounds are supernatants. stream are chemical manufacturing wastes formed in the chlorinator, and are How Many Facilities Generate This that are outside the scope of the Bevill predominantly associated with the Waste Category and How Is It Managed? exemption. exempt mineral processing solids (2) Solids removed from the gaseous (additional details regarding this Four facilities generated commingled titanium tetrachloride stream. These solids wastewaters from the chloride process. are associated with the production of conclusion are provided in the referenced background document). (As will be discussed further in titanium tetrachloride. These solids are III.F.14.e(7), two additional facilities typically slurried to impoundments for These compounds were not assessed, storage or disposal and are Bevill-exempt however, as part of the rulemakings generate the same wastewaters and (with one exception described below). which established the mineral commingle them with wastewaters from (3) Waste acids. In 1990 and 1998 processing exemptions, and so these the sulfate process.) Three of the four rulemakings for LDR Phase IV (see 63 FR results could present new issues for ‘‘chloride only’’ facilities treat their 28601), EPA took the position that the waste these wastes if such compounds were wastewaters in surface impoundment- acids do not meet the high-volume, low- based treatment systems; the fourth toxicity test and thus are not exempt mineral found to pose unacceptable risks. During the development of the mineral facility uses a tank-based wastewater processing wastes. treatment system. Each of the (4) Gases going to scrubbers. Offgases from processing exemption, EPA anticipated the chlorinators pass through various air certain conditions might suggest the impoundment systems include unlined pollution control systems which generate appropriateness of re-opening these units. These large volume wastes are scrubber waters. In 1998, EPA stated that exemptions.48 We are considering generated in excess of 29 million metric scrubber waters and sludges from scrubber whether we should re-assess the status tons per year. These wastewaters are not waters were not Bevill-exempt. However, as of these wastes as exempt mineral Bevill-exempt (but convey exempt a result of the information collection processing wastes. Any reassessment of solids into the wastewater treatment activities associated with today’s proposal, it these wastes would involve a separate system where those solids are removed is now clear to EPA that gases from the to form sludges that are comprised of chlorinator contain some solids from the analysis and opportunity for notice and chlorinator. We are interpreting the comment. exempt solids and non-exempt solids, exemption today to cover these particles depending on the specific piping of the when they drop out of scrubber waters to How Did EPA Assess Mixtures of plants). form sludges. (Gas streams and wastewaters Exempt and Non-Exempt Wastes From Many facilities commingle waste are not Bevill exempt, even when they are the Production of Titanium Dioxide? hydrochloric acids (generated as carrying solid particles from chlorinator.) There are a number of wastes from the scrubber water) with their combined (5) Solids purged from the reactor. A purge titanium dioxide sector that remain wastewaters. Three other facilities, stream from the reactor may be taken to partially within the scope of the consent however, return waste acids on site or reduce silica levels in the reactor. This sell the acids for reuse. Because these stream is Bevill exempt. decree because they are composed of (6) Recovered solids from the reaction area. both exempt and non-exempt solids. materials have no exposure route of Housekeeping results in the collection of Because they are not ‘‘100 percent concern, we did not further evaluate coke and ore solids from the vicinity of the exempt’’ in composition, we have risk scenarios associated with reuse of reaction area. These wastes are Bevill assessed their potential impacts on the this material. exempt. environment, and attempted to isolate In one case, the facility conducts some What Management Scenarios Were the risks associated with the non- Assessed? processing of their ferric chloride waste acid exempt solids and wastewaters. Any (which is subsequently sold as a water and For this rulemaking, we determined wastewater reagent), and generates a solids assessment of the CDD and CDF loading in exempt wastes will involve a separate that the surface impoundment scenario stream. We consider the processing that this poses a more significant potential risk facility conducts to be either an ancillary analysis and opportunity for notice and process or chemical manufacturing, and thus comment. than the tank scenario, and thus the subsequent solids stream is not generated Finally, we are assessing one non- assessed the groundwater pathway for from mineral processing and therefore is not exempt waste generated at the Delaware surface impoundments. We assessed exempt. facility, non-exempt non-wastewaters potential groundwater releases to both surface water and drinking water wells. What Is The Status of the Mineral from the chloride-ilmenite process, We concluded that the air pathway does Processing Exemption for ‘‘Chloride which contains some CDDs and CDFs at not present significant risks for these Waste Solids From Titanium levels exceeding our initial screening wastes because the wastes do not Tetrachloride Production’? criteria. We did not, as part of today’s listing determination, conduct sufficient contain volatile organics or other As part of our waste characterization constituents that pose risk due to air of the titanium dioxide sector, we 48 ‘‘If EPA finds that this exemption is not releases. conducted analyses for chlorinated protective of human health and the environment dibenzo-p-dioxins (CDDs) and dibenzo- and if an examination of titanium tetrachloride How Was This Waste Category p-furans (CDFs). We were concerned waste management shows any continuing or new Characterized? problems, the Agency will reconsider this subtitle that these compounds might be present D determination for chloride process waste solids One of the four facilities, located in in the wastes as a result of the from titanium tetrachloride production.’’ 56 FR Hamilton, Mississippi, was selected for chlorination step which occurs in the 273000, June 13, 1991. sampling and analysis. This facility’s

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TABLE III±40.ÐCHARACTERIZATION OF COMMINGLED WASTEWATERS FROM CHLORIDE PROCESS, TITANIUM DIOXIDE

Detected levels in Sample KM±SI±01 Constituent of concern (mg/L) HBL AWQC SPLP Total Filtrate

Antimony ...... <0.05 0.044 0.006 0.014 Arsenic ...... 0.04 0.001 0.0007 0.000018 Manganese ...... 25.9 0.46 0.73 0.05 Molybdenum ...... 0.53 0.23 0.078 NA Thallium ...... 0.086 1 <0.005 0.001 0.0017 1 Thallium is identified as a potential constituent of concern because it was detected in the totals analysis at levels exceeding the HBL and AWQC, and the SPLP filtrate analysis detection limit was too high to confirm that mobile levels of thallium do not exceed these standards. One half the detection limit was used as input to the risk assessment (see III.E.3).

How Was the Groundwater-to-Surface overall flow being toward the river. We amount of available information best Water Risk Assessment Established? calculated infiltration rates for the supported our data requirements for We assumed that surface unlined impoundment, and divided this modeling and because we believe this impoundments present greater risks to flow rate into the flow rate of the river facility is representative of other the environment than tanks. Therefore to determine potential concentrations of generators of this waste category in we focused on the 3 facilities that the five metals of concern in the river terms of hydrogeological setting and manage wastewaters in impoundments. as a result of recharge with waste characterization. Based on We selected the sampled facility for contaminated groundwater. The results information presented in the RFA for modeling because (1) its management of this screening (see ‘‘Risk Assessment the facility of concern, as well as from practices (i.e., treatment in surface Support to the Inorganic Chemical the U.S. Geological Survey Ground- impoundments) are representative of 3 Industry Listing: Background water Site Inventory, there are of the 4 chloride-only facilities, (2) the Information Document’’) demonstrate groundwater wells north of the plant. that concentrations of the constituents analytical data for this waste were The RFA also indicates that of concern are likely to be well below obtained from this site, and (3) its groundwater flow direction in the setting is similar to the other 2 facilities risk thresholds for both human health and aquatic life in surface water. localized vicinity of the surface that use surface impoundments. The impoundments is to the northwest. We facility selected for modeling is How Was the Groundwater Ingestion modeled the potential impact of the bounded on two sides by a river, Risk Assessment Established? unlined portion of the surface tributary creeks, and swamps. The RCRA Facility Assessment 50 for this site We were able to collect specific impoundment train on drinking water provides maps showing distances to information regarding the physical wells located within 2,000–5,000 feet these potential receptors and setting of the modeled facility, and thus (based on well locations and the closest groundwater flow directions in the used primarily site-specific data as facility property lines). The resultant vicinity of the surface impoundments input to the risk assessment. We chose concentrations are presented below in and plant-wide flow directions, with the this site for modeling because the Table III–41.

TABLE III±41.ÐGROUNDWATER PATHWAY RISK ASSESSMENT RESULTS FOR COMMINGLED WASTEWATERS FROM CHLORIDE PROCESS, TITANIUM DIOXIDE

Risk or hazard quotient Constituent of concern 90th% 95th% Adult Child Adult Child

Antimony HQ ...... 0.1 0.2 0.2 0.5 Arsenic cancer risk ...... 2E±08 2E±08 8E±08 6E±08 Molybdenum HQ ...... 0.03 0.07 0.06 0.1

50 U.S. EPA RCRA Facility Assessment of Kerr 49 This facility also commingles wastewaters from McGee Chemical Corporation; Hamilton, MS. June sodium clorate production, which account for 16, 1995. approximately 1.7 percent of the total 4aste volume.

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TABLE III±41.ÐGROUNDWATER PATHWAY RISK ASSESSMENT RESULTS FOR COMMINGLED WASTEWATERS FROM CHLORIDE PROCESS, TITANIUM DIOXIDEÐContinued

Risk or hazard quotient Constituent of concern 90th% 95th% Adult Child Adult Child

Thallium HQ ...... 0.02 0.03 0.03 0.07

What Is EPA’s Listing Rationale for This contributions of non-exempt solids to wastewater treatment solids are Waste? their waste solids. Two of these described separately in section facilities, both located in Ohio, We propose not to list commingled III.F.14.e(8). They contain significant commingle wastewaters from oxidation wastewaters from the production of volumes of non-exempt solids (>35%). and finishing (i.e., generated after the titanium dioxide via the chloride (3) Various sands from oxidation, production of titanium tetrachloride and process. The results of our risk milling and scouring. therefore potentially bearing non- assessment show that this waste exempt solids) with the wastewaters How Many Facilities Generate This category does not pose significant risk to from titanium tetrachloride production Waste Category and How Is It Managed? human health and the environment. Our that bear exempt solids. Neither facility assessment of the air and surface water Two facilities using the chloride reported any solids in their oxidation exposure pathways shows no risk of process reported disposal of 250 MT of and finishing wastewaters, although concern. Our assessment of the milling sand in off-site and dedicated data from similar wastewaters from the groundwater exposure pathway on-site Subtitle D landfills. One facility chloride-ilmenite process indicate that also reported landfilling over 2,300 MT similarly shows no risk of concern for very low levels of solids can be present the constituents of concern. of scouring sand. One facility reported in similar wastewaters. (We assess 6,935 MT/yr of waste oxidation sand (2) Chloride process solids (Bevill solids from the chloride-ilmenite that is managed in an on-site industrial exempt). Six facilities generate waste process in section III.F.14.e(10) of this Subtitle D landfill. All of these sands are solids from the chloride process. As proposal.) At the third facility (located similar and are associated with titanium previously discussed, the Agency in Mississippi), which operates a dioxide finishing operations. All of determined at 56 FR 27312 (June 13, slightly different process, there were no these sands are produced after the 1991) that chloride process waste solids reported wastewaters or solids from beginning of chemical manufacturing from titanium tetrachloride production oxidation and finishing. Note that the and therefore are not exempt. are Bevill exempt mineral processing wastewaters bearing the exempt solids wastes (40 CFR 261.4(b)(7)(ii)(S)). Five at this facility are commingled with What Management Scenarios Were of the six facilities generate their solids comparatively small volumes of Assessed? in surface impoundments; the sixth, wastewaters from sodium chlorate We assessed the off-site industrial located in Louisiana, uses tank-based production (described in section III.F.11 landfill scenario for milling sand and a settling to segregate the solids from their 52 of today’s proposal). We believe that dedicated on-site landfill for scouring wastewaters. All six facilities dispose of the contribution of any non-exempt sand, reflecting the types of their solids in their surface solids to the volume of exempt solids management reported for these wastes. impoundments or on-site landfills. from these three facilities would be very We assessed the groundwater ingestion Approximately 1.2 million MT of this small. Thus, we have chosen not to pathway for these landfills. The on-site waste was generated in 1998.51 The attribute any risks to the nonexempt landfill scenario for scouring sand waste solids at each of these sites portion of these commingled solids. screened out when we compared the contains contributions from Bevill Two of the six facilities generating SPLP results for this waste directly to exempt solids ranging from 100% to chloride process waste solids also the HBLs. 40%, as discussed further below. operate sulfate-based titanium dioxide At the two facilities located in Georgia production lines. These plants are sited How Was This Waste Category and Louisiana, coke and ore solids are in Georgia and Maryland. Wastewaters Characterized? generated as entirely segregated wastes from the chloride process and sulfate We collected samples of both the that are not commingled with non- processes are commingled and results in milling sand and the scouring sand. We exempt solids; these exempt wastes are commingled wastewater treatment conducted total, TCLP and SPLP clearly outside the scope of the consent solids that are partially composed of analyses on the waste matrix. We used decree dictating today’s proposal and exempt solids. The non-exempt the SPLP results (rather than the TCLP) have not been assessed further. to assess potential releases to 52 At three other facilities, the facilities The sodium chlorate wastewaters account for groundwater because there is no contact conduct some commingling of their only 1.7% of the total volume of managed wastewater, and for only 4.4% of the solids with municipal landfill leachate in the wastewaters, resulting in small potential generated. The predominant potential constituent of reported management practices, and no concern in the sodium chlorate solids is chromium; indication that other practices are likely. 51 This waste volume includes the non-exempt analytical data for the commingled solids (KM–SI– sulfate solids generated at one of the 2 facilities that 04) show that the SPLP concentration is <0.05 mg/ The SPLP analytical results of concern commingle wastes from the chloride and sulfate L and not of concern. See section III.F.11 for further for the milling sand are presented below processes. discussion of this facility’s sludge. in Table III–42.

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TABLE III±42.ÐCHARACTERIZATION OF acid directly to their gypsum plants pathways. The primary gypsum MILLING SAND FROM TITANIUM DI- where it is neutralized to form gypsum. contained lower levels of leachable OXIDE PRODUCTION We found no significant potential for metals than the secondary gypsum; we release of this acid waste prior to its focused our modeling efforts on the Detected treatment in the gypsum plant. The two higher volume secondary gypsum as it SPLP lev- HBL facilities reported production of 69,500 was more likely to show risk when Constituent of concern els in MT/yr of gypsum that is landfilled.53 KP±SO± (mg/L) modeled and the management scenarios 05 (mg/L) We chose to look further at this material are identical (they are placed in the because it is disposed of in a landfill same on-site industrial landfill). The Antimony ...... 0.024 0006 and used in a manner constituting screening results are discussed further disposal (i.e., as fertilizer), and because in the ‘‘Titanium Dioxide Listing the generators conduct on-site land How Was the Groundwater Ingestion Background Document for the Inorganic Risk Assessment Established? placement (piles). Specifically, the Georgia facility places their gypsum in Chemical Listing Determination,’’ As described in Section III.D.4. we piles prior to sale for use in agricultural available in the docket for today’s used our standard distance-to-well chemicals, cement, chemical products, notice. assumptions for an off-site landfill, and and wall board. The Maryland facility assumed hydrogeologic conditions We assessed the landfill scenario for generates primary and secondary would be comparable to those for the potential impacts to both surface water gypsum, both of which are also placed reported off-site landfill. As shown in and drinking water wells. The facility in piles prior to use in wall board Table III–43, the resultant risks were selected for modeling is bounded to the manufacture or disposal in an on-site calculated. north and east by the Patapsco River, landfill. As described above, the which is an estuary. The expected gypsum is not an exempt mineral TABLE III±43.ÐGROUNDWATER PATH- groundwater flow, while not processing waste because this sulfate characterized definitively, is expected to WAY RISK ASSESSMENT RESULTS process wastestream did not meet the be eastward, toward the river.54 FOR MILLING SAND FROM TITANIUM high volume/low toxicity criteria noted DIOXIDE PRODUCTION in 54 FR 36592 (September 1, 1989). How Was This Waste Category Characterized? Antimony HQ What Management Scenarios Were Assessed? Adult Child We collected three samples of this Percentile risk risk We assessed each of the reported waste for analysis. We conducted total, management scenarios that involve land TCLP and SPLP analyses on the waste 90th ...... 0.003 0.006 placement: agricultural chemicals, matrices. We used the SPLP results 95th ...... 0.008 0.02 cement, piles and landfills. We (rather than TCLP) to assess potential evaluated potential releases to both air releases to groundwater and surface What is EPA’s Listing Rationale for This and groundwater. Samples were water because there is no contact with Waste? collected at both facilities, and included municipal landfill leachate in the We propose not to list this waste both primary and secondary gypsum reported management practices. We because the modeled and screening risk samples at the Maryland site. The used total results to assess potential air for antimony, the sole constituent of management scenarios were assessed releases, and this pathway screened out. using the appropriate sample for the concern, is well below a hazard quotient The SPLP analytical results for the type of gypsum reported for that of unity. secondary gypsum that we used to (4) Gypsum from the sulfate process. scenario. All pathways screened out assess groundwater releases from except for the landfill scenario at the How Many Facilities Generate This Maryland site. For the Maryland landfill landfilling are presented below in Table Waste Category and How Is It Managed? we found constituent concentrations at III–44. The Maryland and Georgia facilities levels of potential concern for the generate this waste. Both sites pipe their groundwater and surface water

TABLE III±44.ÐCHARACTERIZATION OF SECONDARY GYPSUM FROM SULFATE PROCESS, TITANIUM DIOXIDE

Detected SPLP levels Constituent of concern in MI±SO± HBL AWQC 03 (mg/L) (mg/L) (mg/L)

Antimony ...... 0.055 0.006 0.014 Arsenic ...... <0.0035 0.0007 0.000018 Manganese ...... 3.1 0.73 0.05

53 Additional volumes are used as products. Department of the Environment. RCRA Operation (now Millennium Inorganic Chemicals, Inc.); 54 See ‘‘Update of the Hazardous Waste and Maintenance Inspection of SCM Chemicals Hawkins Point Plant; Baltimore, MD. October 1994. Groundwater Task Force’’, April 1998. Maryland

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How Was the Groundwater-to-Surface concentrations of the constituents of area to the south of the facility, or that Water Risk Assessment Established? concern are expected to be well below potentially contaminated groundwater We calculated infiltration rates for the risk thresholds for human health and would not reach this neighborhood. We unlined landfill, and divided this flow aquatic life in surface water. thus decided to model potential rate into the flow rate of the river to How Was the Groundwater Ingestion exposure at this neighborhood. We determine potential concentrations of Risk Assessment Established? modeled the potential impact of the the three metals of concern (see Table unlined landfill on drinking water wells III–44) in the river as a result of recharge While we are not aware of any actual located within 2,500–5,000 feet (based with contaminated groundwater. The drinking water wells in the vicinity of on distances to the nearest residential results of this screening (available in the the Maryland facility, we were unable to area). The resultant risks were Risk Assessment Background determine definitively that there are not calculated and are summarized in Table Document) demonstrate that private wells in use in the residential III–45.

TABLE III±45.ÐGROUNDWATER PATHWAY RISK ASSESSMENT RESULTS FOR SECONDARY GYPSUM FROM SULFATE PROCESS, TITANIUM DIOXIDE

Antimony HQ ArsenicÐcancer risk Manganese HQ Adult risk Child risk Adult risk Child risk Adult risk Child risk

90th ...... 0.23 0.49 6.E±07 4.E±07 0.1 0.2 95th ...... 0.35 0.75 1.E±06 1.E±06 0.1 0.3

What is EPA’s Listing Rationale for This (5) Digestion scrubber water from the section III.F.14.e(7). We also modeled Waste? sulfate process. the dedicated surface impoundment We propose not to list gypsum from How Many Facilities Generate This scenario using the physical parameters the sulfate process. The results of our Waste Category and How Is It Managed? describing the dedicated Georgia risk assessment demonstrate that there impoundment. This impoundment is is no significant risk associated with The Maryland and Georgia facilities placed directly on the banks of a river, this material, and that it does not reported generation of digestion and thus we were primarily concerned warrant control as a listed hazardous scrubber water from the sulfate process. with potential releases to surface water. waste. At the 95th percentile, the risks The Maryland facility manages this We did not model a drinking water well for antimony (HQ=0.75) and arsenic wastewater in a dedicated surface scenario because there are no ¥ (1E 6), approach levels at which EPA impoundment after neutralization. The constituents of concern in this considers listing wastes (HQ=1.0 and other facility commingles this wastewater at levels exceeding HBLs. cancer risk>10¥6, respectively). We wastewater with other wastewaters from believe that our modeled exposure their chloride and sulfate processes. As How Was This Waste Category scenario, while plausible, contains a described above, the gypsum is not an Characterized? number of conservative assumptions exempt mineral processing waste that likely overstate these marginal because this sulfate process wastestream We collected one sample of this waste risks. In particular, our assumptions did not meet the high volume/low for analysis. We conducted total regarding groundwater flow direction toxicity criteria noted in 54 FR 36592 analyses (leaching was not conducted (i.e., that a contaminated plume from (September 1, 1989). (See 40 CFR given the low levels of percent solids in the landfill would flow to the south 261.4(b)(7)(ii).) this waste), which are summarized below in Table III–46 for the toward the nearest residences, rather What Management Scenarios Were constituents of potential concern. than due west toward the river) and the Assessed? use of groundwater for drinking water at these residences (records indicate this We assessed the waste in its community uses public water) may commingled form as managed by the overstate actual risks. Maryland facility, as described below in

TABLE III±46.ÐCHARACTERIZATION OF DIGESTION SCRUBBER WATER FROM SULFATE PROCESS, TITANIUM DIOXIDE

Detected levels in HBL AWQC Constituent of concern MI±WW±03 (mg/L) (mg/L) (mg/L)

Aluminum ...... 0.58 16 0.087 Manganese ...... 0.58 0.73 0.05 Mercury ...... 0.0032 0.005 0.000050

How Was the Groundwater-to-Surface of the river to determine potential screening (available in the Risk Water Risk Assessment Established? concentrations of the three metals of Assessment Background Document) concern (see Table III–46) in the river as demonstrate that concentrations of the We calculated infiltration rates for the a result of recharge with contaminated constituents of concern are likely to be unlined surface impoundment, and divided this flow rate into the flow rate groundwater. The results of this

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00073 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55756 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules well below risk thresholds for human facility manages it in a dedicated the levels of constituents in the health and aquatic life in surface water. surface impoundment and the Maryland wastewater were below HBLs and facility places it in an on-site landfill. What is EPA’s Listing Rationale for This AWQC. We modeled the landfill As described above, the waste is not an Waste? scenario for potential releases to both exempt mineral processing waste groundwater drinking wells and surface We propose not to list digestion because this sulfate process wastestream water. scrubber water from the production of did not meet the high volume/low titanium dioxide via the sulfate process. toxicity criteria noted in 54 FR 36592 How Was This Waste Category The results of our risk assessment show (September 1, 1989). (See 40 CFR Characterized? that this waste category does not 261.4(b)(7)(ii).) warrant listing as a hazardous waste. We collected one sample of this waste (6) Sulfate process digestion sludges. What Management Scenarios Were for analysis at the Maryland facility. We Assessed? conducted total, TCLP, and SPLP How Many Facilities Generate This We assessed both management analyses. We used the SPLP results as Waste Category and How Is It Managed? scenarios using the respective samples inputs to the on-site landfill, which are The Maryland and Georgia facilities collected at each facility. The surface summarized below in Table III–47 for generate this sludge. The Georgia impoundment scenario screened out; the constituents of potential concern.

TABLE III±47.ÐCHARACTERIZATION OF DIGESTION SLUDGE FROM SULFATE PROCESS, TITANIUM DIOXIDE

Detected SPLP Lev- Constituent of concern els in MI± HBL (mg/L) AWQC SO±02 (mg/L) (mg/L)

Aluminum ...... 2.0 16 0.087 Antimony ...... 0.023 0.006 0.014 Copper ...... 0.37 1.3 0.0031 Iron ...... 12.0 5 1 Lead ...... 1 0.004 0.015 0.0025 Manganese ...... 0.36 0.73 0.05 Vanadium ...... 0.42 0.14 Zinc ...... 0.30 4.7 0.12 1 Results are less than the typical laboratory reporting limit, but are greater than the calculated instrument detection limits.

How Was the Groundwater-to-Surface (8). The results of this screening ingestion scenario was assessed for Water Risk Assessment Established? (available in the Risk Assessment antimony and vanadium because the Background Document) demonstrate detected SPLP concentrations exceeded We calculated infiltration rates for the that concentrations of the constituents their respective HBLs. We did not assess landfill, and divided this flow rate into of concern are likely to be well below the iron HBL exceedence because the the flow rate of the river to determine risk thresholds for human health and HBL is at or above the solubility limit potential concentrations of the three aquatic life in surface water. in ground water under most conditions. metals of concern (see preceding table) in the river as a result of recharge with How Was the Groundwater Ingestion The resultant risks were calculated and contaminated groundwater. Note that Risk Assessment Established? are summarized in Table III–48. this is the same Maryland landfill See the comparable discussion for the described elsewhere in III.F.14.e(4) and gypsum (III.F.14.e(4)). The groundwater

TABLE III±48.ÐGROUNDWATER PATHWAY RISK ASSESSMENT RESULTS FOR DIGESTION SLUDGE FROM SULFATE PROCESS, TITANIUM DIOXIDE

Antimony HQ Vanadium HQ Adult risk Child risk Adult risk Child risk

90th ...... 0.13 0.27 0.02 0.03 95th ...... 0.18 0.39 0.03 0.07

What Is EPA’s Listing Rationale for This How Many Facilities Generate This sludges that are comprised of exempt Waste? Waste Category and How Is It Managed? solids and non-exempt solids, We propose not to list this waste. The The Maryland and Georgia facilities depending on the specific piping of the results of our risk assessment modeling generate this waste category. Both plants). show that this waste does not contain facilities neutralized their commingled What Management Scenarios Were mobile metals that are likely to pose risk wastewaters and manage them in Assessed? to human health and the environment surface impoundments prior to NPDES due to transport through the subsurface. discharge (but convey exempt solids We collected samples at both facilities (7) Commingled wastewaters from the into the wastewater treatment system at the influent to their surface chloride and sulfate process. where those solids are removed to form impoundment trains. We screened the

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TABLE III±49.ÐCHARACTERIZATION OF COMMINGLED WASTEWATERS FROM CHLORIDE AND SULFATE PROCESS, TITANIUM DIOXIDE [mg/L]

Detected levels in sample Constituent of concern MI±WW±04 HBL AWQC Total SPLP Filtrate

Arsenic ...... 0.022 <0.005 (1) 0.0007 0.000018 Manganese ...... 119 9.95 0.73 0.05 Thallium ...... 0.005 0.004 0.001 0.0017 (1) 1/2 the detection limit was used as input to the risk assessment.

How Was the Groundwater-to-Surface of recharge with contaminated How Was the Groundwater Ingestion Water Risk Assessment Established? groundwater. The results of this Risk Assessment Established? screening (available in the Risk We calculated infiltration rates for the See the comparable discussion for the surface impoundment, and divided this Assessment Background Document) gypsum (III.F.14.e(4)). The resultant flow rate into the flow rate of the river demonstrate that concentrations of the risks were calculated and are to determine potential concentrations of constituents of concern are likely to be the two metals of concern (see well below risk thresholds for human summarized in Table III–50. preceding table) in the river as a result health and aquatic life in surface water.

TABLE III±50.ÐGROUNDWATER PATHWAY RISK ASSESSMENT RESULTS FOR COMMINGLED WASTEWATERS FROM CHLORIDE AND SULFATE PROCESSES, TITANIUM DIOXIDE

90th percentile 95th percentile Constituent of concern Adult Child Adult Child

Arsenic cancer risk ...... 5E±08 3E±08 2E±07 1E±07 Manganese HQ ...... 0.009 0.02 0.02 0.04

What Is EPA’s Listing Rationale for This sludges in on-site landfills. Over slurry and scrubber water from the Waste? 159,000 MT of this waste was generated reaction area) as identified in We propose not to list commingled in 1998. 261.4(b)(7)(ii)(S) and discussed above in wastewaters from the production of What Is the Bevill Exemption Status of III.F.14.e(2). Two scrubber waters from 55 titanium dioxide from the chloride and This Waste Category? the calcination and finishing portion sulfate processes. The results of our risk of the sulfate process contribute non- assessment demonstrate that this waste As discussed above, the chloride exempt solids to the wastewater category does not pose risks warranting process waste solids are exempt mineral treatment solids (sulfate process wastes listing as hazardous waste. Arsenic processing wastes, to the extent that levels at the receptor result in cancer they are associated with the titanium 55 Although wastes from calcining are generally risks well below 1E–06, and manganese tetrachloride process. Data provided by treated as Bevill exempt extraction/beneficiation levels at the receptor are similarly well these two facilities, however, show that wastes, wastes from titanium dioxide calcination these waste contain at least 35% non- are post-mineral processing, chemical below a hazard quotient of one. manufacturing wastes. The Agency noted at 54 FR (8) Wastewater treatment sludges from exempt solids. Our quantitative 36619, ‘‘As discussed in the April NPRM, the commingled chloride-and sulfate- assessment of the potential risk Agency considers any operations following the process wastewaters. associated with these non-exempt solids initial [mineral] processing operation to be is provided here. [mineral] processing operations, regardless of How Many Facilities Generate This whether the activity was included on the list of RTC The wastewater treatment solids at beneficiation activities or has traditionally been Waste Category and How Is It Managed? the Maryland site are derived from at considered beneficiation.’’ Therefore, since mineral processing ends and chemical manufacturing starts Two facilities, sited in Georgia and least four primary sources. Two at the beginning of oxidation, and the calcining step Maryland, generate this waste category, residuals from the chloride process occurs after oxidation, all wastes generated from the and after de-watering, place their contribute exempt solids (i.e., solids calcining step are non-exempt wastes.

VerDate 112000 20:03 Sep 13, 2000 Jkt 190000 PO 00000 Frm 00075 Fmt 4701 Sfmt 4702 E:\FR\FM\14SEP2.SGM pfrm12 PsN: 14SEP2 55758 Federal Register / Vol. 65, No. 179 / Thursday, September 14, 2000 / Proposed Rules are not exempt because, as described estimate that their wastewater treatment ‘‘Titanium Dioxide Listing Background above, the sulfate process wastestreams solids are significantly more than 35% Document for the Inorganic Chemical did not meet the high volume/low non-exempt. Listing Determination’’ for details of this toxicity criteria noted in 54 FR 36592 What Management Scenarios Were screening). (September 1, 1989)). Additional Assessed? potential sources of minor amounts of How Was This Waste Category solids are other wastewaters that are We collected samples of both Characterized? facilities’ wastes and therefore assessed treated in this facility’s wastewater Both facilities were selected for treatment system, including cooling the management practices at the two sites individually. The Maryland facility sampling and analysis. Both samples water, stormwater, drainage water and were collected from filter cake discharge landfill leachate. Based on the treats its wastewater in surface impoundments; the sludge is generated of the filter press. We conducted total, information reported in this facility’s TCLP and SPLP analyses on the waste § 3007 survey response, we estimate that from a filter press, and the facility then places the sludge in an on-site landfill. matrix. We used the SPLP results (rather their wastewater treatment solids are than the TCLP) to assess potential more than 35% non-exempt. We assessed potential groundwater releases to both surface water and releases to groundwater and surface The wastewater treatment solids at drinking water wells from this landfill. water because there is no potential for the Georgia site are derived from at least The Georgia facility dredges its sludge contact with municipal landfill leachate six sources. Two residuals from the from its surface impoundments, filter in the reported management practices chloride process contribute exempt presses the solids, places the filter for these two facilities. Given the large solids (i.e., waste acid from the chloride solids in piles for further drainage and waste quantities reported for this reaction area and supernatant from the air drying, and then places the filter category, we believe it would be chloride solids impoundment) solids in an industrial on-site landfill. prohibitively expensive for off-site (261.4(b)(7)(ii)(S)). Finishing We assessed the groundwater pathways disposal to occur. We used total results wastewaters from the chloride process for the landfill and pile, and the air to assess potential air releases from the contribute non-exempt solids (these pathway for the pile. (Note that we piles, and found no significant risks. wastewaters are generated from the elsewhere assess the groundwater The SPLP analytical results used to chemical manufacturing end of the impact of the Maryland surface assess groundwater releases at the production process). At least three impoundments using sampling data for Maryland facility that generates wastewaters from the sulfate process the wastewater in that unit. See commingled chloride/sulfate contribute non-exempt solids. Based on III.F.14.e(7)). All pathways for the wastewater treatment sludge (as the information reported in this Georgia facility screened out and are not described in the previous paragraph) are facility’s § 3007 survey response, we discussed further in this notice (see the presented below in Table III–51.

TABLE III±51.ÐCHARACTERIZATION OF COMMINGLED WASTEWATER TREATMENT SLUDGES FROM CHLORIDE AND SULFATE PROCESSES, TITANIUM DIOXIDE

Detected SPLP levels Constituent of concern in MI±SO± HBL AWQC 01 (mg/L) (mg/L) (mg/L)

Aluminum ...... 0.24 16 0.087 Arsenic ...... 1 0.00005 0.0007 0.000018 Manganese ...... 2.63 0.73 0.05 Thallium ...... 1 0.003 0.001 0.0017 1 Estimated results are less than the typical laboratory reporting limit, but are greater than the calculated instrument detection limits.

In addition to the metals described of magnitude), which segregates the screening (available in the Risk above, our analytical data show that this majority of its exempts solids from its Assessment Background Document) waste contains polychlorinated dioxins wastewater treatment solids. demonstrate that concentrations of the and furans (PCDD/F). These data are constituents of concern are likely to be How Was the Groundwater-to-Surface provided in the background document well below risk thresholds in surface Water Risk Assessment Established? for the titanium dioxide sector. As water. discussed previously (III.F.14.d), we The Maryland facility selected for How Was the Groundwater Ingestion believe that these contaminants are modeling this scenario was also Risk Assessment Established? clearly associated with the exempt modeled for several other wastes, and is solids contained in this waste, and thus described further in section III.F.14.e(5) The facility selected for modeling this we did not assess them. Samples above. We calculated infiltration rates scenario was also modeled for several collected at these two facilities bear out for the unlined landfill, and divided this other wastes, and is described further in this association with the exempt solids. flow rate into the flow rate of the river section III.F.14.e(4) above. The resultant The Maryland facility, which does not to determine potential concentrations of risks were calculated and are segregate any of its exempt solids from the four metals of concern (see summarized in Table III–52. other wastewater treatment solids, has preceding table) in the river as a result significantly higher PCDD/F levels than of recharge with contaminated the Georgia facility (i.e., several orders groundwater. The results of this

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TABLE III±52.ÐGROUNDWATER PATHWAY RISK ASSESSMENT RESULTS FOR COMMINGLED WASTEWATER TREATMENT SLUDGES FROM CHLORIDE AND SULFATE PROCESSES, TITANIUM DIOXIDE

Manganese HQ Thallium HQ Adult risk Child risk Adult risk Child Risk

90th ...... 0.1 0.3 0.1 0.3 95th ...... 0.2 0.5 0.2 0.4

What Is EPA’s Listing Rationale for This rather than the storage of products, What Is the Bevill Status of Solids Waste? because of their potential for releases to Removed From This Waste? We are proposing not to list the environment.56 In addition, we Prior to disposal or reuse of their commingled wastewater treatment sampled the ferric chloride at the waste acids, both the Mississippi and sludges from chloride and sulfate Delaware facility and found that it Tennessee plants filter their waste acid processes because our modeling of contains a variety of metals, as well as to remove the exempt solids. At the potential groundwater releases shows some chlorinated dioxins and furans. Delaware site, however, the waste acid no risk at levels which warrant listing (See the background document for this is processed via the addition of a this waste as hazardous. No scenario sector for more details on this sampling chemical prior to solids removal. The modeled (groundwater-to-surface water and analysis). These factors may lead to purpose of the chemical addition is to and groundwater-to-drinking water concerns about the legitimacy of the use modify the properties of the waste acid wells) showed risk at levels of of this material as a drinking water and to enhance its value as a saleable regulatory concern. wastewater treatment reagent. However, potable water and wastewater treatment (9) Waste acid (ferric chloride) from as explained below, we do not need to reagent. the chloride-ilmenite process. resolve this issue to make a decision The addition of this chemical at the Delaware plant marks the end of How Many Facilities Generate This about listing ferric chloride. titanium tetrachloride production (i.e., Waste Category and How Is It Managed? This waste routinely exhibits the mineral processing) and the beginning All three facilities that utilize the characteristic of corrosivity and the of ferric chloride production (assuming chloride-ilmenite process generate this toxicity characteristic for chromium and ferric chloride is a legitimate product). waste category. The DeLisle, Mississippi lead. All three generators of the ferric Ferric chloride production can be facility identifies the waste as chloride waste acid acknowledge the considered either chemical characteristic for corrosivity, chromium hazardous nature of this waste. Each manufacturing 57 or an ancillary and lead and disposes of its waste in an generator reported pH levels at 1 or less, process.58 Consequently, as explained on-site underground injection well. The and the one facility that disposes of this below in section III.F.14.e(10), solids Tennessee facility pipes its ferric waste via deep well injection assigns removed from the ferric chloride at the chloride to an on-site sodium chloride three separate characteristic codes to Delaware plant are not Bevill-exempt. plant. Both the Mississippi and this material. EPA sampled the ferric Tennessee facilities generate the What Is EPA’s Listing Rationale for This majority of their exempt-mineral chloride at the Delaware facility, and Waste? processing solids from the filtration of both EPA and the facility analyzed the We are proposing to not list this waste this waste acid. The Delaware facility’s waste. The results showed that this and rely instead on the existing process is slightly different in that the material exhibits the characteristics of regulatory controls provided by the majority of their exempt solids are D001, D007, and D008. hazardous waste characteristics. Data generated prior to the generation of the What Is the Bevill Status of This Waste? from all three facilities clearly waste acid, and only a relatively small demonstrates that this waste exhibits portion of their solids are generated Ferric chloride waste acid is a liquid several of the characteristics. At this from the removal of solids from this mineral processing waste that did not time we have not determined whether waste. The Delaware facility adds a meet the high volume/low toxicity any of the facilities are out of processing chemical to their waste acid, criteria for determining eligibility for compliance. State and EPA authorities removes solids, stores the acid in tanks the Bevill exemption and therefore is are examining these sites in detail for (as well as an on-site surface not Bevill-exempt (see 63 FR 28601). compliance with the existing impoundment when their tank capacity regulations. Listing would not serve to is exceeded), and sells the acid to a better establish this jurisdiction. 56 Surface impoundments pose essentially broker for resale as a wastewater and inherent risks of groundwater contamination due to The Mississippi facility that injects drinking water treatment reagent. the hydraulic pressure created by the contained this waste identifies the waste as However, EPA is not at this time liquids. Management v. EPA, 919 hazardous and manages it as a assessing whether the ferric chloride is F.2d 158, 166 (D.C. Cir. 1992). Material that is hazardous waste under Subtitle C a legitimate product. We did not attempt placed in a surface impoundment, where it is regulations. Within the context of this to address this complex and site-specific capable of posing a substantial present or potential consent decree, we did not investigate hazard to human health or the environment when issue in this proposal. We note that the improperly treated, stored, transported or disposed in depth the Tennessee facility’s use of Delaware facility uses a surface of or otherwise managed, ‘‘by leaching into the this material in production of sodium impoundment to store a portion of the ground, is ‘discarded material’ and hence a solid ferric chloride prior to its sale as a water waste.’’ (AMC II, 907 F.2d) Although secondary 57 54 FR 36616, September 1, 1989. and wastewater treatment reagent. EPA materials may have value and be reused, their value 58 All wastes from ancillary activities are not does not protect them from being considered solid uniquely associated with extraction/beneficiation has often considered land-based units, wastes for the purposes of RCRA regulation if they and processing of ores and minerals (see 45 FR and impoundments in particular, to be are discarded prior to use (API, 906 F.2d at 741 76619, November 19, 1980, and 63 FR 28590, May associated with the discard of wastes, n.16). 26, 1998).

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As each of the three chloride-ilmenite scrubbers at various points in its discussed previously, the Delaware facilities is described below. process. Some solids make their way facility stores the material in a surface All three facilities generate non- into scrubber waters. When the facility impoundment. EPA can address exempt vanadium waste when they treats these wastewaters, the solids concerns, if appropriate, by the use of separate vanadium compounds from precipitate and the resultant wastewater enforcement, based on the existing titanium tetrachloride. The facilities treatment solids are added to the two characteristics associated with this reinsert these materials into the reaction wastes described above to form ‘‘Iron material. In addition, the questions area. Titanium tetrachloride is Rich’’. Solids from the scrubber used to framed above about the potential recovered and maybe reused; however, treat gasses from the titanium legitimacy of this facility’s use of ferric the remainder of this waste is not reused tetrachloride reactor are Bevill-exempt. chloride as a product and its storage in and is incorporated into the unreacted Solids from scrubbers associated with a surface impoundment are equally coke and ore solids stream from the oxidation and finishing (steps that take relevant whether the ferric chloride is reaction area, the solids separated from place after the formation of titanium listed as a hazardous waste or is known the ferric chloride, or the ferric chloride. tetrachloride) are not exempt. Based on to exhibit the characteristics of This vanadium waste is not exempt facility data, we estimate that hazardous waste. Therefore we have because it is not a solid. However we approximately 1.5% of the total volume decided to not list this waste as a were not able to determine the volume of ‘‘Iron Rich’’ consists of non-exempt hazardous waste and rely on the contribution of this vanadium waste to solids from wastewater treatment. hazardous characteristics of the material the various wastes into which it is The Tennessee facility generates for any necessary control. ultimately incorporated. Hence, the solids from ferric chloride filtration and (10) Non-exempt nonwastewaters estimates of total exempt solids from wastewater treatment. The filter from the chloride-ilmenite process. provided below are likely to be solids are exempt (261.4(b)(7)(ii)(S)) underestimated. (This waste is also because such filtration simply removes How Many Facilities Generate This discussed in III.F.14.e(14) below.) exempt solids. Unlike the processing Waste Category and How Is It Managed? The Delaware facility combines and that occurs at the Delaware plant, no All three chloride-ilmenite facilities neutralizes three sources of solids chemical manufacturing is taking place generate wastes that contain (reactor solids, solids removed from at this step at the Tennessee plant. The commingled exempt and non-exempt ferric chloride waste acid, and solids facility landfills these ferric chloride components. Depending on the specific from wastewater treatment), and solids as a discrete wastestream; we do configuration of the individual plants, markets the resulting material as ‘‘Iron not assess this exempt waste further in these wastes are composed to different Rich’’ material. As asserted by the this rule. This facility commingles degrees of exempt and non-exempt company, uses of Iron Rich include wastewaters from both the titanium solids, as described further below. structural fill, landfill caps and covers, tetrachloride and titanium dioxide sides Solids are generated in several places and construction of dikes for of the process, and the resultant in the chloride ilmenite process: containment of dredged spoils on the wastewater treatment sludge is thus Delaware River. The facility may also comprised of exempt and non-exempt —Coke and ore solids are removed from stabilize some portion of the Iron Rich sources. The Tennessee facility reported the gaseous titanium tetrachloride with fly ash prior to sale. Each estimated percent solids data for most of product stream, quenched and component of the Delaware commingled their wastewaters. We reviewed these neutralized. While the Agency residuals is described in the following data and determined that a significant believes this stream is largely exempt, paragraphs. portion (74%) of the resultant sludge we note that any contributions to this The majority of the commingled would be nonexempt (see Titanium stream from the disposal of the Delaware solids are unreacted coke and Dioxide Listing Background Document vanadium waste is non-exempt. ore materials that are removed from the for calculations). These nonexempt —Solids are generated during gaseous titanium tetrachloride product solids are within the scope of today’s wastewater treatment and are non- stream after the reactor. These ‘‘reactor proposal. We sampled the commingled exempt to the extent they are solids’’ make up more than 80% of the exempt and nonexempt waste and generated from oxidation and volume of commingled ‘‘Iron Rich’’ at describe our assessment of this material finishing wastewaters. this facility. This stream is comprised of in this section. —Coke and ore solids can also be exempt chloride process solids and non- The Mississippi facility also generates generated from the removal of solids exempt vanadium waste. exempt solids from filtering ferric from waste acid. These residuals may The Delaware facility also removes chloride prior to deep well injection. No contain a non-exempt portion if they solids from its ferric chloride. This chemical manufacturing occurs. These are partially comprised of vanadium solids removal step takes place after the solids are placed in a dedicated on-site waste. These solids cannot be exempt facility incorporates a chemical additive landfill, and are not assessed further in if they are removed from the waste into the ferric chloride. We have this rule. The facility also operates a acid after the initiation of chemical concluded that the use of this chemical wastewater treatment system which is manufacturing and/or ancillary constitutes chemical processing that is similar to the Tennessee facility in that operations. outside the scope of the Bevill it commingles wastewaters from We assessed these various sources of exemption (see 54 FR 36592, September condensation and purification non-exempt materials as one waste 1, 1989 and previous waste acid (associated with the titanium category because of the expected discussion in III.F.14(e)(9)). In addition, tetrachloride production process), as similarities among these materials and this stream is partially derived from the well as oxidation and finishing

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(associated with the titanium dioxide What Management Scenarios Were relevant. Our assessment addresses the production process). The commingled Assessed? municipal scenario qualitatively. These wastewaters are managed in on-site scenarios were assessed for potential surface impoundments and the dredged The Delaware facility asserts that releases to drinking water wells and air solids from these units (comprised of there are a variety of end uses for the releases. In addition, we modeled the exempt and nonexempt materials) are Iron Rich. The predominant recent use on-site landfill at the Tennessee facility placed in an on-site landfill. The facility has been for the construction of dikes to for potential releases to surface water. contain dredged river sediments at U.S. provided detailed information regarding Army Corp of Engineer disposal sites in How Was This Waste Category the amounts of solids present in each of the vicinity of the titanium dioxide Characterized? the wastewaters managed in this system, plant. We assessed this scenario as demonstrating that there is a small We collected samples of this waste at comparable to an industrial D landfill the Tennessee and Delaware facilities. contribution (∼3%) of non-exempt scenario. The Iron Rich has also been For the Tennessee facility, we collected solids (i.e., solids in wastewaters from used as daily cover at a municipal the sample directly from a holding/ oxidation and finishing) in the landfill (demonstration project) and as dewatering pond where the dredged wastewater treatment sludge. We did final cover for a closed on-site landfill. wastewater treatment solids are not select this facility for site visits and These uses clearly constitute disposal. dewatered prior to landfilling on site. thus did not sample this waste. We Other proposed uses include use as We collected the sample from the believe our sampling and modeling of subsidence fill at a closed municipal Delaware facility directly from the Iron the Tennessee and Delaware sites is an landfill, structural fill by the local Port Rich dewatering unit press; this sample appropriate surrogate for this waste Authority, surcharge for road bed consisted of commingled chlorinator given the similar nature of the processes compaction, and construction of a solids, ferric chloride solids, and at the three facilities (with particular wildlife refuge at the site of the closed wastewater treatment solids. This similarities between the wastewater on-site industrial landfill. These uses all material is sometimes mixed with fly treatment facilities at Mississippi and involve placement on the ground and ash prior to use; our sample was Tennessee). Furthermore, the also appear to also be uses that collected prior to fly ash addition. Both percentages of non-exempt solids in the constitute disposal (see 40 CFR 266.20). samples were analyzed for total, TCLP commingled wastes at the Tennessee We chose to model risks for disposal in and SPLP constituent analyses. These and Delaware sites are higher than at the an off-site industrial D landfill because data are summarized below in Table III– Mississippi site. this seemed to fit the largest number of 54 for the constituents of concern that the varied potential disposal or land- were present in the wastes at levels based use scenarios. We believe the exceeding the health-based levels and/ municipal landfill scenario is also or ambient water quality criteria.

TABLE III±54.ÐCHARACTERIZATION OF WASTEWATER TREATMENT SOLIDS FROM THE CHLORIDE-ILMENITE PROCESS, TITANIUM DIOXIDE

Detected levels, Delaware site Detected levels, AWQC Soil Tennessee site HBL (mg/L) screening Constituent of concern Total TCLP SPLP (mg/L) levels Total SPLP Human Aquatic 1 (mg/kg) (mg/L) (mg/L) (mg/kg) (mg/L) health life (mg/kg)

Antimony ...... 0.9 2 0.021 0.02 0.7 0.021 0.006 0.014 n/a 32 Arsenic ...... 2.2 <0.0035 2 0.001 2.8 3 <0.0035 0.0007 1.8E±05 0.15 4.7 Barium ...... 178 2 2.4 0.92 49.6 0.12 1.1 n/a n/a 5600 Boron ...... 30 1.7 0.61 24.5 0.45 1.4 n/a n/a 7,200 Lead ...... 309 2 0.032 2 0.0032 42.4 2 0.002 0.015 ...... 0.0025 400 Manganese ...... 10,600 252 16.3 2,890 1.5 0.7 0.05 n/a 4 3,800 Nickel ...... 91.8 0.5 <0.005 59.8 0.007 0.31 0.61 0.052 1,600 Thallium ...... 3.7 0.28 0.012 7.2 <0.0022 0.001 0.0017 n/a 6.4 Vanadium ...... 240 2 0.0003 <0.005 1,060 <0.005 0.14 n/a n/a 720 n/a: not applicable. 1 Soil ingestion health-based levels. 2 Results are less than the typical laboratory reporting limit, but are greater than the calculated instrument detection limits. 3 One half the detection limit was used as model input. 4 The air characteristic level is 3,000 mg/kg at 25m and drops to 30,000 at 150m.

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In addition, our analytical data show TABLE III±55.ÐCHARACTERIZATION OF flow will generally follow the natural that chlorinated dioxins and furans are WASTEWATER TREATMENT SOLIDS topography. A ridgeline running north present in these wastes. As discussed FROM THE CHLORIDE-ILMENITE and south is located just east of the previously, we believe these compounds PROCESS, TITANIUM DIOXIDE facility boundary. This ridge is are associated with the exempt solids. approximately 200 feet higher in CHLORINATED DIBENZO-P-DIOXINS However, the Delaware waste contains elevation than the elevation at the the ferric chloride solids; these solids (CDD) AND FURANS (CDF)ÐCon- facility. Based on this topography, we have lost their exempt status because of tinued expect that the groundwater flow the facility’s chemical manufacturing/ direction is to the west towards the ancillary activities necessary for the Total De- tected levels river. We calculated the concentrations production of ferric chloride for sale as in Delaware in the river that would result from a water and wastewater treatment Constituent of concern waste discharge of contaminated ground water reagent. As a result, we have considered (ng/kg, wet by estimating the infiltration rate for the the chlorinated dioxin and furan basis) unlined landfill, and (given the area of content of the waste as part of today’s 1234789-HeptaCDF ...... 126 the landfill) diluting the resulting listing determination. The PCDD/PCDF OctaCDF ...... 24,000 leachate volume into the river under analytical results for the Delaware site OctaCDD ...... 22.2 various design flow conditions. The are summarized below (detected 2378±TetraCDD Equivalent1 .... 57.2 results of this screening level analysis homologs only) in Table III–55. (available in the Risk Assessment 1 12378±TetraCDD equivalent calculated using the World Health Organization Toxic Background Document) demonstrate TABLE III±55.ÐCHARACTERIZATION OF Equivalency Factors (WHO±TEF). Van den that concentrations of the constituents WASTEWATER TREATMENT SOLIDS Berg, et al. 1998. Toxic Equivalency Factors of concern in the river are likely to be FROM THE HLORIDE LMENITE (TEFs) for PCBs, PCDDs, PCDFs for Human well below the national AWQC for C -I and Wildlife. Environmental Health Perspec- PROCESS, TITANIUM DIOXIDE tives, v.106, n.12, pp. 775±792. December. human health and aquatic life for these CHLORINATED DIBENZO-P-DIOXINS constituents. How Was the Groundwater-to-Surface (CDD) AND FURANS (CDF) Water Risk Assessment Established? How Was the Groundwater Ingestion Risk Assessment Established? Total De- The Tennessee facility is bounded to tected levels the west by the Tennessee River. The The Delaware facility reported actual in Delaware facility indicated that the overall or contemplated use of the Iron Rich at Constituent of concern waste (ng/kg, wet groundwater flow is toward the river. a variety of landfills and land placement basis) There have been several projects to usages in the general vicinity of the determine placement of down gradient plant. We used our usual distance-to- 2378-TetraCDF ...... 12.2 monitoring wells for individual on-site well assumptions for an off-site landfill, 12378-PentaCDF ...... 21.8 landfill units. These borings indicate and assumed hydrogeologic conditions 23478-PentaCDF ...... 48.1 that the groundwater elevation declines 123478-HexaCDF ...... 237 that are representative of the principal 123678-HexaCDF ...... 8.1 to the northwest towards the river. In soil and aquifer types present regionally 234678-HexaCDF ...... 2.5 addition, a contract geologist familiar (within a 100 mile radius) of the facility. 123789-HexaCDF ...... 5.6 with the local hydrogeology has The resultant risk assessment results are 1234678-HeptaCDF ...... 189 indicated that shallow groundwater presented below in Table III–56.

TABLE III±56.ÐGROUNDWATER PATHWAY RISK ASSESSMENT RESULTS FOR NON-WASTEWATERS FROM CHLORIDE- ILMENITE PROCESS, TITANIUM DIOXIDE

Hazard quotient or cancer risk Constituents of concern 90th% adult 90th% child 95th% adult 95th% child

Antimony ...... 0.2 0.5 0.4 0.8 Arsenic (cancer risk) ...... 3E±07 2E±07 1E±06 9E±07 Manganese ...... 0.8 1.6 1.6 3.3 Thallium ...... 0.7 1.4 1.1 2.4

What Is EPA’s Listing Rationale for This these listed materials remain In addition, the management practices Waste? commingled with solids that would reported for this waste, particularly as otherwise be exempt, the entire reported for the Delaware site, are We propose to list as hazardous the commingled mass is subject to the expected to provide less control than non-exempt portion of the solid wastes listing (see § 261.3(b)(2)). Our risk the scenario modeled (i.e., an industrial generated from the production of results indicate that metals in these landfill). Potential future management titanium dioxide via the chloride- materials leach at levels that may pose practices include use at municipal ilmenite process. This listing covers the a risk to human health and the landfills for interim and final cover, as non-exempt portions of the wastewater environment. Specifically, in the well as subsidence fill at a closed treatment solids generated at all three commingled wastes, the risks exceed an municipal landfill. These scenarios, facilities, any non-exempt portions of HQ of one for both manganese (3.3) and particularly the interim cover scenario, the chlorinator solids (e.g., any mass thallium (2.4) at the 95th percentile; the indicate that the waste may come in derived from the vanadium wastes), and risks similarly exceed an HQ of one for contact with municipal landfill leachate ferric chloride solids generated at the both manganese (1.6) and thallium (1.4) in the future, if not listed. The TCLP Delaware facility. To the extent that at the 90th percentile. results for this waste indicate even

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TABLE III±57.ÐREDUCED VOLUME ANALYSIS; GROUNDWATER PATHWAY RISK ASSESSMENT RESULTS FOR NON- WASTEWATERS FROM CHLORIDE-ILMENITE PROCESS, TITANIUM DIOXIDE

Hazard quotient or cancer risk Constituents of concern 90th % adult 90th % child 95th % adult 95th % child

Antimony ...... 0.1 0.2 0.2 0.4 Arsenic ...... not modeled Manganese ...... 0.5 1.0 1.0 2.2 Thallium ...... 0.4 0.9 0.8 1.6

This waste also contains 57 ppt TCDD (these solids were part of the Iron Rich (11) HCl from reaction scrubber, equivalents. This concentration exceeds sample collected by EPA to support this chloride-ilmenite process. All three the background level in soils (8 ppt) and listing determination). Similarly, at the chloride-ilmenite facilities reported the soil ingestion HBL of 45 ppt59. We Delaware facility, solids that collect in generating HCl from scrubbing reactor were not able to compare this the ferric chloride product storage tanks off-gasses. These wastes are stored in concentration with a screening level and impoundments would be covered covered tanks with vent scrubbers and from the Air Characteristics Study by the listing as these solids are are re-used on site, predominantly as pH because the study did not establish ineligible for the mineral processing control in wastewater treatment levels for TCDD. While we did not exemption (because they are generated systems. We assessed this waste as part conduct a risk assessment of the after the initiation of chemical of the following category, ‘‘Commingled detected TCDD TEQ, the presence of manufacturing and/or ancillary wastewaters from chloride-ilmenite TCDD equivalents in the wastes is an operations), they are comparable to the process’’. additional factor that supports a listing ferric chloride solids that are determination, particularly in light of commingled in the Iron Rich, and they (12) Commingled wastewaters from the fact that the management practices are derived to some degree from non- the chloride-ilmenite process. reported by the facility were varied and, exempt vanadium materials. The How Many Facilities Generate This in many cases, would constitute releases proposed listing, therefore, reads: Waste Category and How Is It Managed? to the circulating environment with a K178 Non-wastewaters from the production greater potential for a variety of of titanium dioxide by the chloride- All three chloride-ilmenite facilities exposure pathways than would occur ilmenite process. (T) [This listing does not commingle their wastewaters and treat from a well managed landfill. apply to chloride process waste solids from them on-site. The Delaware facility The proposed listing address all non- titanium tetrachloride production exempt utilizes a tank-based system, with final wastewaters that are not covered by the under section 261.4(b)(7)] NPDES discharge through an unlined mineral processing waste exemption, cooling pond to the adjacent river. Both and is not limited to non-exempt We are also proposing to add the Tennessee and Mississippi facilities wastewater treatment solids. The listing manganese and thallium to Appendix utilized surface impoundment based therefore would cover non-exempt non- VII to Part 261, which designates the wastewater treatment systems. These hazardous constituents for which K178 wastewaters from the removal of wastewaters are not Bevill-exempt (but would be listed. In addition, we are vanadium wastes from the product convey exempt solids into the proposing to add manganese to the list titanium tetrachloride stream that are wastewater treatment system where of hazardous constituents in Appendix currently returned to the reaction area those solids are removed to form VIII to Part 261. We believe the available and ultimately commingled with the sludges that are comprised of exempt exempt reactor solids or ferric chloride studies clearly show that manganese has toxic effects on humans and other life solids and non-exempt solids, 60 depending on the specific piping of the 59 forms. EPA is currently evaluating the health risks plants). from 2,3,7,8-TCDD and once the review process is completed, EPA may re-examine the soil ingestion 60 See information in EPA’s IRIS database, which HBL. See http://www.epa.gov.ncea.dioxin.htm for may be found at http://www.epa.gov/iris, and ‘‘Risk for the Inorganic Chemical Manufacturing Wastes’’ additional information. Assessment Support to the Listing Determinations (August 2000) in the docket for today’s rule.

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What Management Scenarios Were potential drinking water wells. The the Mississippi facility’s surface Assessed? RFI 61 for this site indicates that the impoundments on surface water local groundwater flow is generally because the facility is bounded to the We modeled the surface toward the south and east. It is unclear south by the Bay of St. Louis. impoundment scenarios at both the what the patterns are off site and how We did not conduct sampling and Tennessee and Mississippi sites. (We these patterns might change seasonally, analysis at the Mississippi facility. Our assumed any releases from the unlined but the groundwater elevation maps risk assessment inputs for this facility cooling pond at the Delaware facility included in the RFI indicated that the used the combined analytical data set would be intercepted by the river, and direction of groundwater flow does vary for the Delaware and Tennessee would be comparable in concentration, seasonally and that a shift to a more facilities, which are sister plants of the but much less volume than the actual westerly direction may occur under NPDES discharge point.) some conditions. Information from the Mississippi plant. We used the physical At the Tennessee site, we assessed the U.S. Geological Survey’s Ground-water parameters for the Mississippi site to potential releases from the Site Inventory, available in the docket describe wastewater flows, surface impoundment system to the adjacent for today’s proposal, shows numerous impoundment sizes, and distances to river. We do not believe any drinking drinking water wells in the vicinity of potential receptors for this modeling. water wells could possibly be impacted the plant, both to the east and How Was This Waste Category by these impoundments given their southwest. The facility also reported Characterized? placement on the river banks and within wells on their property which they the facility property. We sampled at this believe are cross-gradient and, in some The analytical results for the facility at the headworks to the cases, unused. We chose to model the constituents found to be present in the impoundment train. groundwater scenario because of wastewaters at levels exceeding HBLs We assessed the Mississippi facility’s potential impacts on these known wells. and/or AWQC are presented below in impact on both surface water and We also assessed the potential impact of Table III–58.

TABLE III±58.ÐCHARACTERIZATION OF COMMINGLED WASTEWATERS FROM CHLORIDE-ILMENITE PROCESS, TITANIUM DIOXIDE

Detected Detected levels in levels in AWQCÐ Constituent of concern Delaware Tennessee HBL Aquatic life sample sample (mg/L) (mg/L) (mg/L) (mg/L)

Aluminum ...... 0.65 3.1 16 0.087 Copper ...... 0.03 0.007 1.3 0.0031 Lead ...... <0.003 0.005B 0.015 0.0025 Manganese ...... 3.3 3.34 0.73 N/A Nickel ...... 0.013 0.020 0.3 0.052 Thallium ...... <0.005 0.013 0.001 N/A Vanadium ...... 0.018 0.63 0.14 N/A B: also detected in blank N/A: not available

How Was the Groundwater-to-Surface unlined surface impoundment, and How Was the Groundwater Ingestion Water Risk Assessment Established? (given the area of the impoundment) Risk Assessment Established? diluting the resulting leachate volume The Tennessee facility is bounded to Based on information presented in the the west by a river. As noted above, the into the river under various design flow RFI for the Mississippi facility, as well facility indicated that the overall conditions. The results of this screening as from the U.S. Geological Survey groundwater flow is toward the river. level analysis (available in Risk Ground-water Site Inventory, there are The Mississippi facility is bounded to Assessment Support to the Inorganic groundwater wells to the east and the south by the Bay of St. Louis, which Chemical Industry Listing: Background southwest of the plant within 2,000– is fed by 2 rivers to the east and west Information Document’’) demonstrate 5,000 feet. We modeled the potential of the plant. Additional details are that concentrations of the constituents impact of the unlined surface available in the docket. We calculated of concern in the river are likely to be impoundment train on drinking water the concentration in the river that well below the human health and wells located within this range. The would result from discharge of aquatic life AWQC for these results are presented below in Table III– contaminated groundwater by constituents. 59. estimating the infiltration rate for the

61 Draft RCRA Facility Investigation Report; DuPont DeLisle, NS. December 7, 1999.

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TABLE III±59.ÐGROUNDWATER PATHWAY RISK ASSESSMENT RESULTS FOR COMMINGLED WASTEWATERS FROM CHLORIDE-ILMENITE PROCESS, TITANIUM DIOXIDE

Hazard quotient Constituent of concern 90th % adult 90th % child 95th % adult 95th % child

Manganese ...... 0.0002 0.0003 0.0003 0.0007 Thallium ...... 0.002 0.004 0.004 0.009 Vanadium ...... 0.00009 0.0002 0.0003 0.0006

What Is EPA’s Listing Rationale for This therefore, contamination of ground How Many Facilities Generate This Waste? water is not likely to pose a significant Waste Category and How is it Managed? We propose not to list commingled risk to human health. Based on this fact, and the very small volume generated by Two facilities reported generating this wastewaters from the production of waste, although we believe that all titanium dioxide via the chloride- one facility, we propose not to list this material as a hazardous waste. titanium dioxide manufacturers may ilmenite process. The results of our risk generate this waste at some time. The assessment demonstrate that this waste (14) Vanadium waste from the chloride-ilmenite and chloride process. two reporting facilities both describe category poses no risks that warrant off-site Subtitle D landfills that accept listing as hazardous waste. The Vanadium containing material is generated from the production of both municipal and industrial wastes as concentrations of the constituents of the final management practice for this concern at the modeled exposure points titanium dioxide via the chloride and waste. As noted in the September 1, are well below an HQ of one. the chloride-ilmenite processes. This is 1989 Bevill rulemaking, off- (13) Additive vent filter solids from not an exempt mineral processing waste specification commercial product the chloride-ilmenite process. One because it is not a solid (see also 63 FR wastes are non-exempt solid wastes. facility reported production of vent 28602). This waste is generally returned filter solids from additive handling. to the reaction area where titanium What Management Scenarios Were This material is placed in an off-site tetrachloride is recovered and the Assessed? industrial D landfill. Small amounts of remainder of the vanadium waste is this waste are generated (<1 MT). This incorporated into the mass of the We modeled the off-site municipal D material is not Bevill exempt. Handling unreacted coke and ore solids (i.e., the landfill scenario using the regional of this additive is an ancillary activity. exempt solids) and/or the waste acid. locations of the reported landfills. All wastes from ancillary activities are There is no potential for exposure prior How Was This Waste Category not uniquely associated with extraction/ to mixing with the exempt waste or Characterized? beneficiation and processing of ores and waste acid. We assessed the mixtures of minerals (see 45 FR 76619, November exempt and non-exempt wastes as We collected one sample of this waste 19, 1980, and 63 FR 28590, May 26, discussed above in III.D.14.e(8) and (10). and conducted totals, TCLP, and SPLP 1998). Specifically, we assessed the wastewater analyses. The analytical results for the Information from the facility indicates treatment solids at the Maryland one constituent found to be present in that a constituent of concern in this facility, the Iron Rich material at the the waste TCLP sample at a level material is aluminum. The drinking Delaware facility, and the waste acid. exceeding its HBL are presented below water HBL for aluminum is higher than (15) Off-specification titanium in Table III–60 (no constituent exceeded the solubility limit in ground water and, dioxide product. HBLs in the SPLP).

TABLE III±60.ÐCHARACTERIZATION OF OFF-SPECIFICATION TITANIUM DIOXIDE PRODUCT

Detected levels in sample Constituent of concern DPN±SO±02 (mg/L) HBL (mg/L) Total TCLP

Lead ...... 0.6 1 0.06 0.015 1 Results are less than the typical laboratory reporting limit, but are greater than the calculated instrument detection limits.

How Was the Groundwater Ingestion our usual distance-to-well assumptions a 100 mile radius) for the particular Risk Assessment Established? for an off-site landfill, and assumed landfill sites that were reported for these hydrogeologic conditions that are wastes. The resultant groundwater The facilities reported use of landfills representative of the principal soil and concentrations were very low and are in the vicinity of their plant. We used aquifer types present regionally (within presented below in Table III–61.

TABLE III±61.ÐGROUNDWATER PATHWAY RISK ASSESSMENT RESULTS FOR OFF-SPECIFICATION TITANIUM DIOXIDE

Predicted well concentrations (mg/L) HBL Constituent of concern (mg/L) 90th% 95th%

Lead ...... 2.5E±08 1.1E±06 0.015

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The modeled levels of lead were so far Of course, as set out in detail in the propose deferrals for similar wastes below the HBL that we determined it August 1988 notice, this does not mean derived from landfills. was unnecessary to further assess the that landfills holding wastes that are At the time this issue was brought to risks from lead. Clearly those risks listed now as hazardous become subject the Agency’s attention in the context of would be well below an HQ of one. to Subtitle C regulation. However, the petroleum refinery waste listings, previously disposed wastes now What Is EPA’s Listing Rationale for This meeting a listing description, including EPA’s Office of Water had recently Waste? residues such as leachate that are proposed national effluent limitations guidelines and pretreatment standards We propose not to list off- derived from such wastes, and that are for wastewater discharges—most specification titanium dioxide as a managed actively do become subject to notably, leachate—from certain types of hazardous waste. Our risk analysis Subtitle C regulation. See 53 FR at shows that this waste does not pose 31149, August 17, 1988. In many, landfills. See 63 FR 6426, February 6, risks that warrant listing. indeed most, circumstances, active 1998. In support of this proposal, EPA management of leachate would be conducted a study of the volume and (16) Railcar/trailer product washout. exempt from Subtitle C regulation chemical composition of wastewaters One facility reported generation of this because the usual pattern of generated by both subtitle C (hazardous residual (<10,000 MT). The washwater, management is discharge either to waste) and subtitle D (non-hazardous containing titanium dioxide, is placed POTWs via the sewer system, where waste) landfills, including treatment in a surface impoundment. This waste leachate mixes with domestic sewage is not Bevill exempt because it is a technologies and management practices and is excluded from RCRA jurisdiction currently in use. Most pertinent to liquid and it is associated with the (see RCRA Section 1004(27) and 40 CFR chemical manufacturing part of the finalizing the temporary deferral for the 261.4(a)(1)), or to navigable waters, also petroleum refining wastes, EPA did not process. The water from this pond is excluded from RCRA jurisdiction (see subsequently sent to wastewater propose (or subsequently finalize) RCRA Section 1004(27) and 40 CFR pretreatment standards for subtitle D treatment where it is commingled with 261.4(a)(2)). In addition, management of landfill wastewaters sent to POTWs all other chloride-ilmenite wastewaters leachate in wastewater treatment tanks (assessed in III.D.14.e(12)). The titanium prior to discharge under the CWA is because the Agency’s information dioxide product that settles to the exempt from RCRA regulation (40 CFR indicated that such standards were not bottom of this pond is mechanically 264.1(g)(6)). required (see 65 FR 3008, January 19, recovered and returned to the If actively managed, landfill leachate 2000). production process. We assessed the and gas condensate derived from the The conditions included in the potential impact of this impoundment newly-listed wastes proposed for listing temporary deferral we published on via the SPLP analytical data collected in today’s proposal could be classified February 11, 1999 are that the leachate for off-specification product (previously as K176, K177, or K178. In such is subject to regulation under the Clean discussed in III.D.14.e(15)). These data circumstances, we would be concerned Water Act, and the leachate cannot be are available in the background about the potential disruption in current document for this sector, and show no stored in surface impoundments after leachate management that could occur, February 13, 2001. See 40 CFR constituents of concern. We chose the and the possibility of redundant 261.4(b)(15). We believe that it was SPLP to assess this management regulation. This issue was raised to the appropriate to temporarily defer the scenario because there is no potential Agency in the context of the petroleum for contact with municipal landfill refinery waste listings (see 63 FR 42173, application of the new waste codes to leachate. We therefore do not propose to August 6, 1998). A commenter such leachate in order to avoid list this waste. expressed concern that, because some of disruption of ongoing leachate the commenter’s non-hazardous waste management activities while the Agency G. What Is the Status of Landfill decides if any further integration is Leachate From Previously Disposed landfills received newly-listed needed of the RCRA and CWA Wastes? petroleum wastes prior to the effective date of the listing decision, the leachate regulations consistent with RCRA Leachate derived from the treatment, that is collected and managed from Section 1006(b)(1). We believe that it is storage, or disposal of listed hazardous these landfills would be classified as still appropriate to defer regulation and wastes is classified as a hazardous waste hazardous. The commenter argued that avoid leachate management activities, by virtue of the ‘‘derived-from’’ rule in this could lead to vastly increased and to permit the Agency to decide 40 CFR 261.3(c)(2). The Agency has treatment and disposal costs without whether any further integration of the been clear in the past that hazardous necessarily any environmental benefit. two programs is needed. As such, we waste listings apply to wastes disposed After examining and seeking comment would be concerned about forcing of prior to the effective date of a listing, on this issue, we published a final rule pretreatment of leachate even though even if the landfill ceases disposal of the that temporarily defers regulation of pretreatment is neither required by the waste when the waste becomes landfill leachate and gas condensate CWA, nor needed. Therefore, we are hazardous. (See 53 FR 31147, August derived from certain listed petroleum proposing to temporarily defer the 17, 1988). We also have a well- refining wastes (K169-K172) that were regulation of landfill leachate and gas established interpretation that listings disposed before, but not after, the new condensate derived from the wastes we apply to leachate derived from the listings became effective, provided are proposing for listing in today’s rule, disposal of listed hazardous wastes, certain conditions are met. See 64 FR with the same conditions as described including leachate derived from wastes 6806, February 11, 1999. Since then, we in 40 CFR 261.4(b)(15) for petroleum meeting the listing description that were have published proposed rules for wastes. We seek comment on our disposed before the effective date of a wastes from the dye and pigment listing. We are not reopening any of industries (64 FR 40192, July 23, 1999) proposed decision to extend the these issues with this proposed and the chlorinated aliphatics industry temporary deferral to include the wastes rulemaking. (64 FR 46476, August 25, 1998) that also proposed for listing in today’s notice.

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IV. Proposed Treatment Standards proposed regulated hazardous Therefore, the nonwastewater treatment Under RCRA’s Land Disposal constituents and the proposed treatment standard for antimony is 1.15 mg/L Restrictions limits can be found in the following TCLP, for arsenic is 5.0 mg/L TCLP, and preamble sections and in the proposed for lead is 0.75 mg/L TCLP. In the event A. What Are EPA’s Land Disposal regulatory Table 268.40—Treatment that there are wastewater treatment Restrictions (LDRs)? Standards for Hazardous Wastes. If we residuals from treatment of K177 (which RCRA requires us to establish make a final decision to list the under the derived-from rule also would treatment standards for all wastes identified wastes, these constituents and be considered K177), the wastewater destined for the land disposal. These are treatment standards would apply. treatment standard for antimony is 1.9 the ‘‘land disposal restrictions’’ or LDRs. We have provided in the BDAT mg/L, for arsenic is 1.4 mg/L, and for For any hazardous waste identified or background document a review of lead is 0.69 mg/L. listed after November 8, 1984, we must technologies that can be used to meet We are requesting data and comment promulgate these LDR treatment the proposed numerical concentration on the stabilization of antimony. standards within six months of the date limits for K176, K177, and K178, Available stabilization data for of identification or final listing (RCRA assuming optimized design and antimony show effective treatment for Section 3004(g)(4), 42 U.S.C. 6924(g)(4)). operation. Where we are proposing wastes with initial antimony RCRA also requires us to set as these numerical concentration limits, the use concentrations below those found in treatment standards ‘‘* * * levels or of other technologies capable of K177. Therefore, based on the available methods of treatment, if any, which achieving the proposed treatment data, we are uncertain if stabilization substantially diminish the toxicity of standards would be allowed, except for will be effective for the antimony in this the waste or substantially reduce the those treatment or reclamation practices waste. likelihood of migration of hazardous constituting land disposal or D. What Are the Treatment Standards constituents from the waste so that impermissible dilution (see 40 CFR for K178 (Nonwastewaters From the short-term and long-term threats to 268.3). human health and the environment are Production of Titanium Dioxide by the minimized.’’ (RCRA Section 3004(m)(1), B. What Are the Treatment Standards Chloride-Ilmenite Process)? 42 U.S.C. 6924(m)(1)). for K176 (Baghouse Filters From The constituents of concern in this Once a hazardous waste is prohibited Production of Antimony Oxide)? waste are the chlorinated congeners of from land disposal, the statute provides The constituents identified to require dibenzo-p-dioxin and dibenzofuran, only two options for legal land disposal: treatment in this waste are antimony, thallium and manganese. We are Meet the treatment standard for the arsenic, cadmium, lead, and mercury. proposing to apply the UTS levels to the waste prior to land disposal, or dispose We are proposing to apply the UTS chlorinated congeners of dibenzo-p- of the waste in a land disposal unit that levels to these constituents as the dioxin and dibenzofuran, and thallium, satisfies the statutory no migration test. treatment standards. Therefore, the as indicated in Table V–1. In addition A no migration unit is one from which nonwastewaters treatment standard we are also proposing the option of there will be no migration of hazardous proposed for antimony is 1.15mg/L complying with the technology standard constituents for as long as the waste TCLP; arsenic is 5.0 mg/L TCLP; of combustion (CMBST) for the remains hazardous. RCRA sections 3004 cadmium is 0.11 mg/L TCLP; lead is chlorinated dibenzo-p-dioxin and (d), (e), (f), and (g)(5). Each waste 0.75 mg/L TCLP; and, mercury is 0.025 dibenzofuran (dioxins and furans) identified for listing as hazardous in this mg/L TCLP. In the event that there are constituents present in K178. rule will be subject to all the land wastewater treatment residuals from We note at the outset that we typically disposal restrictions on the same day treatment of K176 (which under the promulgate numerical performance their respective listing becomes derived-from rule would also be standards to allow facilities maximum effective. considered as K176), the wastewater flexibility in determining for themselves We gathered data on waste treatment standards are as follows: how best to achieve compliance with characteristics and current management Antimony is 1.9 mg/L; arsenic is 1.4 mg/ the LDR treatment standards. By practices for wastes proposed to be L; cadmium is 0.69 mg/L; lead is 0.69 promulgating combustion as an listed in this action. These data can be mg/L; and, mercury is 0.15 mg/L. alternative compliance option, we are found in the administrative record for We are requesting data and comment not disturbing the degree of flexibility this rule. An examination of the on the stabilization of antimony. afforded to facilities; rather, we are constituents that are the basis of the Available stabilization data for enhancing it. proposed listings shows that we have antimony show effective treatment for However, when we specify a previously developed numerical wastes with initial antimony treatment technology like CMBST as the treatment standards for most of the concentrations below those found in treatment standard, the analytical constituents. We have determined that it K176. Therefore, based on the available elements of compliance change. is technically feasible and justified to data, we are uncertain if stabilization Typically, with specified technologies, apply existing universal treatment will be effective for the antimony in this no testing and analysis of treatment standards (UTS) to the hazardous waste. residuals is required because we are constituents in the wastes proposed to confident that use of the specified be listed as K176, K177, and K178 that C. What Standards Are the Treatment technology will reduce the level of were found to be present at Standards for K177 (Slag From the target organic constituents to levels that concentrations exceeding the treatment Production of Antimony Oxide That is minimize threats to human health and standards, because the waste Disposed of or Speculatively the environment. For K178, the compositions are similar to other wastes Accumulated)? regulated organic constituents of for which applicable treatment The constituents identified to require concern are dioxin/furan congeners. If technologies have been demonstrated. treatment in this waste are antimony, combustion in well designed and Also see LDR Phase II final rule, 59 FR arsenic, and lead. We are proposing to operated units is used to treat K178, the 47982, September 19, 1994, for a further apply the UTS levels to these dioxin/furan congeners in the K178 discussion of UTS. A list of the constituents as the treatment standards. should be substantially destroyed. By

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To account for this in a manner equivalent to a Part 264 or treatment yielded concentrations of uncertainty, we selected treatment data Part 266 combustion unit. The practical 0.002, 0.003, and 0.46 mg/L TCLP. representing relatively high initial effect of this change will be to limit the Under the LDR program, we typically concentrations (up to 1000 mg/L), but type of facilities that can combust K178 apply a variability factor of 2.8 to the also representing full scale operation to well-regulated RCRA units (or, after treated waste data, to account for and satisfactory treatment (at least 90 the current transition period, Clean Air variations arising from mechanical percent reduction in concentration). We Act permitted units subject to MACT limitations in the treatment equipment. found that sedimentation technology, standards). This will ensure that Therefore we calculated potential the most effective treatment method in combustion is done in a closely- treatment standards based on our database, resulted in a final effluent regulated facility and in a manner that solidification treatment from our concentration of 6.1 mg/L and chemical provides protection for human health treatability database as 0.006, 0.008, and precipitation technology resulted in and the environment. Furthermore, by 1.29 mg/L TCLP. We are unsure whether final effluent concentrations of 2.4 and restricting combustion of K178 to these these treatment standards would be 4.8 mg/L (both operated at full scale and units, combustion will only occur in achievable in a waste with the resulted in greater than 90 percent units subject to the recently upgraded significantly higher concentrations of reduction). We have selected, to be dioxin/furan emission standards of the manganese found in K178. Therefore, conservative, the highest concentration MACT Hazardous Waste Combustion we are not proposing treatment (6.1 mg/L) to calculate a K178 Rule as well as standards for other standards based on solidification. wastewater standard. We applied a hazardous air pollutants, such as metals Rather, to propose a more achievable variability factor of 2.8 to obtain a (64 FR 52828, September 30, 1999). standard, we based it on a technology proposed K178 LDR treatment standard K178 does have metal constituents of which results in higher post-treatment of 17.1mg/L. Again, we request concern, which would not be treated by manganese levels. High temperature comments on and data relevant to this metals recovery (which vitrifies the the combustion process and that would proposed treatment standard for manganese in the slag) resulted in a remain in the combustion treatment wastewater forms of K178, both from treated manganese concentration of 1.3 residuals (e.g., ash and scrubber water). those who support the standard and mg/L TCLP. Using this datum and our We therefore are retaining metal those who believe the standard is not typical variability factor of 2.8, we treatment standards for all achievable. We also request any calculated a proposed manganese circumstances, i.e., whether or not the information regarding the similarity of treatment standard of 3.6 mg/L TCLP. treatment used by a facility involves manganese wastewater treatment to the We request comment and data on this combustion. When combustion is used treatment of other RCRA-regulated proposed treatment standard, and we to treat the organics to achieve LDR metals that now appear in the UTS, both request anyone who has an interest in compliance, facilities will still need to from a structural or physico-chemical the treatment standard for manganese to perspective as well as from a treatment conduct compliance testing and analysis comment to that effect. We may use the performance perspective. Only for all regulated metal constituents in list of commenters on this topic as the commenters on this subject may be the combustion treatment residuals only individuals notified of potential notified of future changes we may make prior to disposal. This approach is changes to this proposed treatment based on newly submitted data. patterned after EPA’s promulgation of a standard, so it is important for you to similar alternative treatment standard comment if you are in any way Because we typically include the for F024 (wastes from production of interested. same treatment standards for new chlorinated aliphatics) and also for F032 Because it is possible that listings into those for F039 (multisource (wastes from wood preserving commenters may submit data showing leachate) to maintain equivalence processes). See 55 FR 22580–81, June 1, that this treatment option is within the LDR regulatory structure, we 1990. See also 62 FR 26000–3, May 12, inappropriate for K178, we request are also proposing to add the manganese 1997. comment on the option of setting a treatment standard to the F039 section For both solid and wastewater treatment standard for manganese that is of the 268.40 table. The F039 waste code treatment residuals, we are proposing identical to the current UTS level for applies to hazardous waste landfill use of the Universal Treatment thallium, the other metal found in leachates in lieu of the original waste Standards (UTS) for all constituents of proposed K178. The thallium treatment codes when multiple waste codes would concern except manganese. Universal level of 0.20 mg/L TCLP is based on otherwise apply. F039 wastes are treatment standards have not been stabilization. We also request any subject to numerical treatment developed for manganese, although we information regarding the similarity of standards equivalent to UTS. We are are proposing standards below. We did manganese nonwastewater treatment to proposing this addition to the not study this constituent in the the treatment of other RCRA-regulated constituents regulated by F039 to development of F039 treatment metals that now appear in the UTS, both maintain the implementation benefits of standards in 1990 or UTS in 1994. from a structural or physico-chemical having one waste code for multisource Furthermore, we lack studies perspective as well as from a treatment leachate. We are also proposing to add demonstrating treatment effectiveness performance perspective. manganese to the UTS Table at 40 CFR for highly concentrated manganese We have some treatment data for 268.48. Manganese represents nonwastewaters, such as those manganese in wastewater matrices significant risk to human health and the containing manganese at levels such as derived from wastes other than K178 in environment, as shown in the risk those found in K178. We did, however, our treatability database. It has been assessment accompanying this rule. Its identify treatability data for less difficult to determine whether these presence in other hazardous wastes

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TABLE IV±1.ÐTREATMENT STANDARDS FOR K178

Regulated hazardous constituent Wastewaters Nonwastewaters Concentration in mg/kg4 un- 1 2 Common name CAS Concentration in mg/L , less noted as No. or technology code 3 ``mg/L TCLP'', or technology code

1,2,3,4,6,7,8-Heptachlorodibenzo-p-dioxin ...... 35822±39±4 0.000035 or CMBST 5 ...... 0.0025 or CMBST 5 1,2,3,4,6,7,8-Heptachlorodibenzofuran ...... 67562±39±4 0.000035 or CMBST 5 ...... 0.0025 or CMBST 5 1,2,3,4,7,8,9-Heptachlorodibenzofuran ...... 55673±89±7 0.000035 or CMBST 5 ...... 0.0025 or CMBST 5 HxCDDs (All Hexachlorodibenzo-p-dioxins) ...... 34465±46±8 0.000063 or CMBST 5 ...... 0.001 or CMBST 5 HxCDFs (All Hexachlorodibenzofurans) ...... 55684±94±1 0.000063 or CMBST 5 ...... 0.001 or CMBST 5 1,2,3,4,6,7,8,9-Octachlorodibenzo-p-dioxin (OCDD) ...... 3268±87±9 0.000063 or CMBST 5 ...... 0.005 or CMBST 5 1,2,3,4,6,7,8,9-Octachlorodibenzofuran (OCDF) ...... 39001±02±0 0.000063 or CMBST 5 ...... 0.005 or CMBST 5 PeCDDs (All Pentachlorodibenzo-p-dioxins) ...... 36088±22±9 0.000063 or CMBST 5 ...... 0.001 or CMBST 5 PeCDFs (All Pentachlorodibenzofurans) ...... 30402±15±4 0.000035 or CMBST 5 ...... 0.001 or CMBST 5 TCDDs (All tetrachlorodi-benzo-p-dioxins) ...... 41903±57±5 0.000063 or CMBST 5 ...... 0.001 or CMBST 5 TCDFs (All tetrachlorodibenzofurans) ...... 55722±27±5 0.000063 or CMBST 5 ...... 0.001 or CMBST 5 Manganese ...... 7439±96±5 17.1 ...... 3.6 mg/L TCLP Thallium ...... 7440±28±0 1.4 ...... 0.20 mg/L TCLP 1 CAS means Chemical Abstract Services. When the waste code and/or regulated constituents are described as a combination of a chemical with its salts and/or esters, the CAS number is given for the parent compound only. 2 Concentration standards for wastewaters are expressed in mg/L and are based on analysis of composite samples. 3 All treatment standards expressed as a Technology Code or combination of Technology Codes are explained in detail in 40 CFR 268.42 Table 1-Technology Codes and Descriptions of Technology-Based Standards. 4 Except for Metals (EP or TCLP) and Cyanides (Total and Amenable) the nonwastewater treatment standards expressed as a concentration were established, in part, based upon incineration in units operated in accordance with the technical requirements of 40 CFR part 264, subpart O or 40 CFR part 265, subpart O, or based upon combustion in fuel substitution units operating in accordance with applicable technical require- ments. A facility may comply with these treatment standards according to provisions in 40 CFR 268.40(d). All concentration standards for nonwastewaters are based on analysis of grab samples. 5 For these wastes, the definition of CMBST is limited to: (1) combustion units operating under 40 CFR 266, (2) combustion units permitted under 40 CFR Part 264, Subpart O, or (3) combustion units operating under 40 CFR 265, Subpart O, which have obtained a determination of equivalent treatment under 268.42(b).

What Other LDR Provisions Are with these wastes would have to be the LDR treatment standards being Proposed to Apply? treated prior to land disposal, meeting proposed today, or if they are disposed 1. Debris. We propose to apply the either alternative treatment standards in a deep injection well that has been regulations at 40 CFR 268.45 to (i.e., 10 times UTS or 90 percent granted a no migration petition for those hazardous debris contaminated with reduction in initial constituent wastes. K176, K177 or K178. Debris concentrations) or the standards at 40 E. Is There Treatment Capacity for the contaminated with these wastes would CFR 268.40 being proposed today. Non- Proposed Wastes? have to be treated prior to land disposal, soil residuals generated from the using specific technologies from one or treatment of soil contaminated with 1. What Is a Capacity Determination? more of the following families of debris K176, K177, or K178 would remain EPA must determine whether treatment technologies: extraction, subject to the treatment standards adequate alternative treatment capacity destruction, or immobilization. proposed today. See 63 FR 28602, May exists nationally to manage the wastes Hazardous debris contaminated with a 26, 1998, for additional information on subject to LDR treatment standards. listed waste that is treated by an the applicability, scope, and content of RCRA section 3004 (h)(2). Thus, LDRs immobilization technology specified in the alternative soil treatment standard are effective when the new listings are 40 CFR 268.45 Table 1 is a hazardous provisions. effective (typically 6 months after the waste and must be managed in a 3. Underground Injection Wells that new listings are published in the hazardous waste facility. Residuals can be found in the administrative Federal Register), unless EPA grants a generated from the treatment of debris record for this rule. Finally, because national capacity variance from the contaminated with K176, K177, or K178 land disposal also includes placement otherwise-applicable date and would remain subject to the treatment in injection wells (40 CFR 268.2(c)) establishes a different date (not to standards proposed today. See 57 FR application of the land disposal exceed two years beyond the statutory 37277, August 18, 1992, for additional restrictions to K176, K177, and K178 deadline) based on ‘‘* * * the earliest information on the applicability, scope, requires the modification of injection date on which adequate alternative and content of the hazardous debris well requirements found in 40 CFR 148. treatment, recovery, or disposal capacity provisions. We propose that K176, K177, and K178 which protects human health and the 2. Soil. In addition, we propose to be prohibited from underground environment will be available’’ (RCRA apply the regulations at 40 CFR 268.49 injection. Therefore, these wastes could section 3004(h)(2), 42 U.S.C.6924(h)(2)). to hazardous soil contaminated with not be underground injected unless they Our capacity analysis methodology K176, K177, or K178. Soil contaminated have been treated in compliance with focuses on the amount of waste

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We also request or K177 that is expected to be generated regulated under NPDES, discharges to a data on soil or debris contaminated with and therefore, there is no quantity of the POTW, or treatment in a RCRA-exempt these wastes, residuals generated from wastewater form of K176 or K177 that tank, is not included in the quantities the treatment or recycling of these will require alternative commercial requiring additional treatment as a wastes, and the current and planned treatment. These wastes are typically result of the LDRs. Also, land-disposed management practices for the wastes, present in a nonwastewater form. Based wastes that do not require alternative or waste mixtures, and treatment residuals. on the RCRA § 3007 Survey information additional treatment are excluded from For available capacity to meet the presented in the Capacity Background the required capacity estimates (i.e., LDR requirements, we request data on Document, required alternative those that currently are treated to meet the current treatment or recovery treatment capacity for K176 the LDR treatment standards). Land- capacity capable of treating these nonwastewaters is estimated to be eight disposed wastes requiring alternative or wastes, facility and unit permit status tons per year. Required alternative additional treatment or recovery related to treatment of the proposed treatment capacity for K177 capacity that is available on site or wastes, and any plans that facilities may nonwastewaters is estimated to be 22 within the same company also are expand or reduce existing capacity or tons per year. As described in the excluded from the required commercial construct new capacity. In addition, we section of proposed LDR treatment capacity estimates. The resulting request information on the time and standards above, we are proposing that estimates of required commercial necessary procedures required for numerical treatment standards be capacity then are compared to estimates permit modification for generators or applied to K176 and K177 of available commercial capacity. If commercial treatment or disposal nonwastewaters. We anticipate that adequate commercial capacity exists, facilities to manage the wastes, required commercially available stabilization, as the waste is restricted from further land changes for operating practices due to well as other technologies, can be used disposal. If protective alternative the proposed listings or proposed in meeting these treatment standards. capacity does not exist, EPA has the additional constituent to be regulated in We estimate that the commercially authority to grant a national capacity the wastes, and any waste minimization available stabilization capacity is at variance. activities associated with the wastes. Of least eight million tons per year based In making the estimates described particular interest to us are chemical on the 1995 Biennial Report. Thus we above, the volume of waste requiring and physical constraints of treatment expect there is sufficient capacity to treatment depends on the current waste technologies for these wastes and any treat the proposed K176 and K177 management practices employed by the problems for disposing of these wastes. hazardous wastes that would require waste generators before this proposed Also of interest are any analytical treatment. Therefore, we are proposing regulation is promulgated and becomes not to grant a national capacity variance difficulties associated with identifying effective. Data on waste management for K176 or K177 wastewaters or and monitoring the regulated practices for these wastes were collected nonwastewaters. constituents in these wastes. during the development of this For K178 waste (chloride-ilmenite proposed rule. However, we realize that F. What are the Capacity Analysis nonexempt nonwastewaters from the as the regulatory process proceeds, Results? production of titanium dioxide), our generators of these wastes may decide to data indicate that the waste is typically minimize or recycle their wastes or This preamble only provides a generated as a nonwastewater. We did otherwise alter their management summary of the capacity analysis not identify any wastewater forms of practices. Thus, we will monitor performed to support this proposed these wastes and therefore do not changes and update data on current regulation. For additional and more anticipate that alternative management management practices as these changes detailed information, please refer to the for wastewaters is required. We found will affect the volume of wastes ‘‘Background Document for Capacity that the wastes are currently land ultimately requiring commercial Analysis for Land Disposal Restrictions: disposed. We estimated that treatment or recovery capacity. Inorganic Chemical Production Wastes approximately 7,300 tons per year The commercial hazardous waste (Proposed Rule),’’ August 2000 (i.e., the (derived from public information since treatment industry may change rapidly. Capacity Background Document). data on amounts of treatment solids are For example, national commercial For this capacity analysis, we confidential as reported in § 3007 treatment capacity changes as new examined data on waste characteristics Survey) may require alternative facilities come on line or old facilities and management practices gathered for treatment. In our assessment, we go off line, and as new units and new the inorganic chemical hazardous waste assumed that facilities can segregate technologies are added at existing listing determinations. We also wastestreams and separately manage the facilities. The available capacity at examined data on available treatment or newly-proposed hazardous waste. commercial facilities also changes as recovery capacity for these wastes. The Although the generation quantity (and facilities change their commercial status sources for these data are the RCRA therefore, the quantity requiring (e.g., changing from a fully commercial Section 3007 Survey distributed in the treatment) may be higher due to the to a limited commercial or ‘‘captive’’— spring of 1999, record sampling and site derived from rule, we expect that company owned—facility). Thus, we visits (see the docket for today’s rule for available treatment capacity still exists. also continue to update and monitor more information on these survey As discussed earlier for K178 changes in available commercial instruments and facility activities), the treatment standards, we are proposing treatment capacity. available treatment capacity data that numerical treatment standards be For wastes required to meet today’s submission that was collected in the applied to K178 wastes. We anticipate proposed treatment standards, we mid-1990’s, and the 1997 Biennial that commercially available request data on the annual generation Report. incineration, followed by stabilization if

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These upper bound estimates are most propose the technology standard of With respect to the revisions to the likely very overstated since only a combustion (CMBST) as an alternative F039 and UTS lists, as discussed earlier portion of each estimated waste volume compliance option for hazardous in the section on K178 treatment may contain manganese at organic constituents in the K178 wastes. standards, we are proposing to add concentrations above the proposed level The units treating the waste by using manganese to the list of regulated specified in the UTS table and the F039 CMBST will be subject to certain constituents in F039 (§ 268.40) and the list. The estimates assume that standards, and facilities will need to UTS table (§ 268.48). We have estimated manganese is present at levels above the meet treatment standards for all what portion of the F039 or proposed treatment standards in all of regulated metal constituents prior to characteristic wastes (which require these wastes and require alternative disposal, as discussed in the earlier treatment of underlying hazardous treatment, when it is likely that this may section on K178 treatment standards. constituents to UTS levels) may be be true in only a small sets of the cases. We assume that facilities would achieve required to meet these new treatment Furthermore, EPA does not anticipate treatment standards using incineration, standards. We request comments on the that waste volumes subject to treatment stabilization, or both. The quantity of estimates, the appropriate means of for F039 or characteristic wastes would commercially available combustion treatment (if necessary), and the significantly increase because waste capacity for sludge and solid is a sufficiency of available treatment generators already are required to minimum of 300,000 tons per year and capacity for the affected wastes by the comply with the treatment requirements the quantity of commercially available addition of manganese to the F039 and for other metals that may be present in stabilization capacity is at least eight UTS lists. the wastes. The volumes of wastes for million tons per year based on 1995 When changing the treatment which additional treatment is needed Biennial Report. requirements for wastes already subject solely due to the addition of manganese We have identified that there exist to LDR (including F039 and to the F039 and UTS lists are therefore characteristic wastes), EPA no longer facilities managing K178 waste in expected to be very small. See the has authority to use RCRA § 3004(h)(2) surface impoundments (i.e., in Capacity Background Document for to grant a capacity variance to these wastewater treatment systems that detailed analysis. contain land based units). If the waste wastes. However, EPA is guided by the overall objective of section 3004(h), However, even though our volume is managed in unretrofitted estimates are highly conservative and impoundments,62 it would thus be land namely that treatment standards which best accomplish the goal of RCRA overstated, we find that there still disposed in a prohibited manner. These would be no shortage of treatment impoundments can be retrofitted, closed § 3004(m) (to minimize threats posed by land disposal) should take effect as soon capacity. Based on data submittals in or replaced with tank systems. If the the mid-1990’s and the 1997 Biennial impoundment continues to be used to as possible, consistent with availability of treatment capacity. Report, EPA has estimated that manage K178 waste, the unit will be approximately 37 million tons per year subject to Subtitle C requirements. In We expect that only a limited quantity of hazardous waste leachate may be of commercial wastewater treatment addition, any hazardous wastes capacity are available, and well over one managed in the affected impoundment generated from the disposal of newly- listed K176, K177, and K178 wastes million tons per year of liquid, sludge, after the effective date of today’s rule are and solid commercial combustion subject to land disposal prohibitions.63 (due to the small number of generators) and added to the generation of leachates capacity are available. Also, as However, facilities may continue to from other multiple restricted hazardous discussed earlier in this section, there manage newly listed K178 in surface wastes already subject to LDR. exist several million tons of available impoundments, provided they are in For the amount of characteristic stabilization capacity. These are well compliance with the appropriate wastes or leachates generated from those above the quantities of F039 or standards for impoundments (40 CFR previously regulated hazardous wastes characteristic wastes potentially Parts 264 and 265 subpart K) and the that would be subject only to the new requiring treatment for manganese even special rules regarding surface treatment standards for manganese, we under the conservative screening impoundments (40 CFR 268.14). EPA evaluated the universe of wastes that assumptions described above. notes that those provisions require basic might be impacted by revisions to the Therefore, we are proposing a decision groundwater monitoring (40 CFR Parts lists of regulated constituents for F039 not to delay the effective date for adding 264 and 265 Subpart F), management, and UTS based on limited information. manganese to the lists of constituents and recordkeeping, but (in keeping with Based on 1997 Biennial Report data and for F039 and UTS. RCRA section 3005(j)(6)(A)) are afforded some assumptions of waste We request comment on its proposed up to 48 months to retrofit to meet compositions and their potential for decision not to delay the effective date minimum technological requirements. land disposal, we were able to estimate for adding manganese to the lists of Based on the foregoing, we expect that the potential need for additional constituents for F039 and UTS. We sufficient capacity to treat the proposed treatment. For example, we estimated an request data on the annual generation K178 hazardous wastes that would upper bound of 70,000 tons per year of volumes and characteristics of wastes require treatment. Therefore, we are nonwastewaters mixed with other waste potentially affected by the proposed codes, the F039 leachate from which changes to UTS and F039 in wastewater 62 A unretrofitted impoundment is one not satisfying the minimum technology requirements would be potentially impacted by the and nonwastewater forms (if any), and (MTR) specified in sections 3004(o) and 3005(j)(11). revision to the F039 treatment the current and planned management 63 See RCRA § 3004(m)(1) ‘‘Simultaneously with standards. In a similar fashion, we practices for the wastes, waste mixtures, the promulgation of regulations under subsection estimated that no more than 520,000 and treatment residuals. We also request (d), (e), (f), or (g) prohibiting one or more methods of land disposal of a particular hazardous waste tons per year of characteristic data on the current treatment or * * * promulgate regulations specifying those nonwastewaters potentially might be recovery capacity capable of treating the levels or methods of treatment * * *’’ affected by the proposed changes (i.e., affected wastes.

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Further, for soil and debris Should this occur, we will revise the requirements were promulgated or contaminated with the newly listed capacity analysis accordingly. enacted, the state was obligated to enact wastes (K176, K177, and K178), we equivalent authority within specified V. Compliance Dates believe that the vast majority of time-frames. New Federal requirements contaminated soil and debris We seek comment on the proposed did not take effect in an authorized state contaminated with these wastes will be decisions in this section. until the state adopted the requirements managed on-site and therefore will not A. Notification as state law. require substantial commercial By contrast, under Section 3006(g) of treatment capacity. Therefore, we are Under the RCRA Section 3010 any RCRA, 42 U.S.C. 6926(g), new not proposing to grant a national person generating, transporting, or requirements and prohibitions imposed capacity variance for hazardous soil and managing a hazardous waste must notify by the HSWA (including the hazardous debris contaminated with these wastes EPA (or an authorized state) of its waste listings in this proposal) take covered under this proposal. Based on activities. Section 3010(a) allows us to effect in authorized states at the same the 1999 RCRA § 3007 Survey followed waive, under certain circumstances, the time that they take effect in non- by record sampling and site visits, there notification requirement under Section authorized states. EPA is directed to are no data showing the newly listed 3010 of RCRA. If these hazardous waste implement those requirements and wastes managed by underground listings are promulgated, we propose to prohibitions in authorized states, injection wells. Also, based on the 1999 waive the notification requirement as including the issuance of permits, until RCRA § 3007 Survey followed by record unnecessary for persons already the state is granted authorization to do sampling and site visits, there are no identified within the hazardous waste so. While states must still adopt HSWA- data showing mixed radioactive wastes management universe (i.e., persons who related provisions as state law to retain associated with the proposed listings. have an EPA identification number final authorization, the Federal HSWA EPA is proposing to not grant a national under 40 CFR 262.12). We do not requirements apply in authorized states capacity variance for underground propose to waive the notification in the interim. requirement for waste handlers who injected wastes, mixed radioactive B. Effect on State Authorizations wastes, or soil and debris contaminated have neither notified us that they may with these mixed radioactive wastes, if manage hazardous wastes nor received Because this proposal (with the such wastes are generated. an EPA identification number. Such exception of the actions proposed under Therefore, we propose that LDR individuals will have to provide CERCLA authority) will be promulgated treatment standards for the affected notification under RCRA Section 3010. pursuant to the HSWA, a state wastes covered under today’s rule thus B. Interim Status and Permitted submitting a program modification is become effective when the listing Facilities able to apply to receive either interim or determinations become effective—the final authorization under Section earliest possible date (see RCRA section Because HSWA requirements are 3006(g)(2) or 3006(b), respectively, on 3004(h)(1)—land disposal prohibitions applicable in authorized states at the the basis of requirements that are must take effect immediately when same time as in unauthorized states, we substantially equivalent or equivalent to there is sufficient protective treatment will regulate the newly identified EPA’s requirements. The procedures capacity for the waste available). wastes listed under HSWA until states and schedule for state program However, we may need to revise are authorized to regulate these wastes. modifications under 3006(b) are capacity analyses or capacity variance Thus, once this regulation becomes described in 40 CFR 271.21. It should be decisions if final listing determinations effective as a final rule, we will apply noted that all HSWA interim are changed or if we receive data and Federal regulations to these wastes and authorizations are currently scheduled information to warrant any revision. to their management in both authorized to expire on January 1, 2003 (see 57 FR Finally, we request comments on the and unauthorized states. 60129, February 18, 1992). estimated quantities requiring VI. State Authority Section 271.21(e)(2) of EPA’s state alternative treatment and information authorization regulations (40 CFR Part on characteristics of the affected wastes, A. Applicability of Rule in Authorized 271) requires that states with final management practices for these wastes, States authorization modify their programs to and available treatment, recovery or Under Section 3006 of RCRA, we may reflect federal program changes and disposal capacity for the wastes. We authorize qualified states to administer submit the modifications to EPA for also request comments concerning and enforce the RCRA program within approval. The deadline by which the alternative management for any of these the state. (See 40 CFR Part 271 for the states must modify their programs to wastes managed in surface standards and requirements for adopt this proposed regulation, if it is impoundments, including new piping authorization.) Following authorization, adopted as a final rule, will be or tank systems, and the length of time we retain enforcement authority under determined by the date of promulgation required for such activities. In addition, Sections 3007, 3008, 3013, and 7003 of of a final rule in accordance with 40 we solicit comments on our decision not RCRA, although authorized states have CFR 271.21(e)(2). If the proposal is to grant a national capacity variance or primary enforcement responsibility. adopted as a final rule, Table 1 at 40 delay the effective date for any of the Before the Hazardous and Solid Waste CFR 271.1 will be amended accordingly. affected wastes. We will consider all Amendments of 1984 (HSWA) amended Once we approve the modification, the available data and information provided RCRA, a state with final authorization state requirements become RCRA during the public comment period and administered its hazardous waste Subtitle C requirements. revise our capacity analysis accordingly program entirely in lieu of the Federal States with authorized RCRA in making the final capacity program in that state. The Federal programs already may have regulations determinations. Please note, the requirements no longer applied in the similar to those in this proposed rule. ultimate volumes of wastes estimated to authorized state, and we could not issue These state regulations have not been require alternative or additional permits for any facilities located in the assessed against the Federal regulations commercial treatment may change if the state with permitting authorization. being proposed to determine whether final listing determinations change. When new, more stringent Federal they meet the tests for authorization.

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Thus, a state would not be authorized to been released in a quantity that is equal chronic toxicity, and potential implement these regulations as RCRA to or exceeds its RQ must immediately carcinogenicity. requirements until state program notify the NRC as soon as that person Generally, for each intrinsic property, modifications are submitted to EPA and has knowledge of the release. The toll- we rank the hazardous substance on a approved, pursuant to 40 CFR 271.21. free telephone number of the NRC is 1– five-tier scale, associating a specific Of course, States with existing 800–424–8802; in the Washington, DC, range of values on each scale with an regulations that are more stringent than metropolitan area, the number is (202) RQ value of 1, 10, 100, 1,000, or 5,000 or broader in scope than current Federal 267–2675. In addition to this reporting pounds. Based on the various primary regulations may continue to administer requirement under CERCLA, Section criteria, the hazardous substance may and enforce their regulations as a matter 304 of the Emergency Planning and receive several tentative RQ values. The of state law. Community Right-to-Know Act of 1986 lowest of the tentative RQs becomes the It should be noted that authorized (EPCRA) requires owners or operators of ‘‘primary criteria RQ’’ for that states are required to modify their certain facilities to report releases of substance. programs only when EPA promulgates extremely hazardous substances and After the primary criteria RQ is Federal standards that are more CERCLA hazardous substances to State assigned, the substance is evaluated stringent or broader in scope than and local authorities. Immediately after further for its susceptibility to certain existing Federal standards. Section 3009 the release of an RQ or more of an degradative processes, which are used of RCRA allows states to impose extremely hazardous substance or a as secondary RQ adjustment criteria. standards more stringent than those in CERCLA hazardous substance, EPCRA These natural degradative processes are the Federal program. For those Federal Section 304 notification must be given biodegradation, hydrolysis, and program changes that are less stringent to the community emergency photolysis (BHP). If a hazardous or reduce the scope of the Federal coordinator of the local emergency substance, when released into the program, states are not required to planning committee for any area likely environment, degrades relatively modify their programs. See 40 CFR to be affected by the release, and to the rapidly to a less hazardous form by one 271.1(I). This proposed rule, if finalized, State emergency response commission or more of the BHP processes, its is neither less stringent than nor a of any State likely to be affected by the primary criteria RQ is generally raised reduction in the scope or the current release. one level. Conversely, if a hazardous Federal program, and, therefore, states Under Section 102(b) of CERCLA, all substance degrades to a more hazardous would be required to modify their product after its release, the original programs to retain authorization to hazardous substances (as defined by CERCLA Section 101(14)) have a substance is assigned an RQ equal to the implement and enforce these RQ for the more hazardous substance, regulations. statutory RQ of one pound, unless and until the RQ is adjusted by regulation. which may be one or more levels lower VII. Designation of Inorganic Chemical In today’s proposed rule, we propose: than the RQ for the original substance. Wastes under the Comprehensive (1) to list the following three The standard methodology used to Environmental Response, wastestreams as RCRA hazardous adjust the RQs for RCRA hazardous Compensation, and Liability Act wastes; (2) to designate these wastestreams differs from the (CERCLA) wastestreams as CERCLA hazardous methodology applied to individual All hazardous wastes listed under substances, and (3) to adjust the one- hazardous substances. The procedure RCRA and codified in 40 CFR 261.31 pound statutory RQs for two of these for assigning RQs to RCRA wastestreams through 261.33, as well as any solid wastestreams. The proposed is based on an analysis of the hazardous waste that is not excluded from wastestreams are as follows: constituents of the wastestreams. The constituents of each RCRA hazardous regulation as a hazardous waste under K176 Baghouse filters from the production wastestream are identified in 40 CFR 40 CFR 261.4(b) and that exhibits one or of antimony oxide more of the characteristics of a RCRA K177 Slag from the production of antimony part 261, Appendix VII. We determine hazardous waste (as defined in 40 CFR oxide that is disposed of or speculatively an RQ for each constituent within the 261.21 through 261.24), are hazardous accumulated wastestream and establish the lowest substances under the Comprehensive K178 Nonwastewaters from the production of RQ value of these constituents as the Environmental Response, titanium dioxide by the chloride-ilmenite adjusted RQ for the wastestream. Compensation, and Liability Act of 1980 process. [This listing does not apply to In today’s proposed rule, we propose (CERCLA), as amended (see CERCLA chloride process waste solids from to assign a one-pound adjusted RQ to Section 101(14)(C)). CERCLA hazardous titanium tetrachloride production exempt the K176 wastestream and 5,000 pounds substances are listed in Table 302.4 at under 40 CFR 261.4(b)(7).] to the K177 wastestream. The proposed 40 CFR 302.4 along with their reportable B. Basis for Proposed RQ Adjustment adjusted RQs for both of these quantities (RQs). If a hazardous wastestreams are based on the lowest substance is released in an amount that Our methodology for adjusting the RQ value of the constituents present in equals or exceeds its RQ, the release RQs of individual hazardous substances each wastestream, are presented in must be reported immediately to the begins with an evaluation of the Table VII–1 below. We seek comment National Response Center (NRC) intrinsic physical, chemical, and our proposed adjustments to the RQ pursuant to CERCLA Section 103. toxicological properties of each values for these wastes. We are not hazardous substance. The intrinsic adjusting the RQ for K178 at this time A. Reporting Requirements properties examined—called ‘‘primary because we have not yet developed a Under CERCLA Section 103(a), the criteria’’—are aquatic toxicity, ‘‘waste constituent RQ’’ for manganese, person in charge of a vessel or facility mammalian toxicity (oral, dermal, and one of the constituents of concern in from which a hazardous substance has inhalation), ignitability, reactivity, this waste.

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TABLE VII±1.ÐPROPOSED ADJUSTED RQS FOR WASTESTREAMS K176, K177, AND K178

Wastestream constituent Wastestream Wastestream Wastestream constituent RQ RQ (lb.) (lb.)

K176 ...... arsenic ...... 1 1 lead ...... 10 ...... K177 ...... antimony ...... 5,000 5,000

VIII. Administrative Assessments followed by a presentation of the cost, The Agency has modeled the most economic impact and benefit results, likely post-regulatory scenario resulting A. Executive Order 12866 may be found in the background from the listing (e.g., disposal in a Under Executive Order 12866, [58 FR document: ‘‘Economic Analysis of the Subtitle C hazardous waste landfill, 51,735 (October 4, 1993)] the Agency Proposed Rule For Listing Hazardous recycling) and estimated the cost of must determine whether the regulatory Waste From Inorganic Chemical complying with it. The difference action is ‘‘significant’’ and therefore Production,’’ which was placed in the between the baseline management cost subject to OMB review and the docket for today’s proposed rule. We and the post-regulatory cost is the requirements of the Executive Order. seek comment on the methodology incremental cost of the rulemaking. The Order defines ‘‘significant used, the projected economic impacts, To estimate the economic impact of regulatory action’’ as one that is likely and the benefits assumed for the today’s proposed rulemaking, we to result in a rule that may: (1) Have an proposed listings. annual effect on the economy of $100 compared the incremental cost of the million or more or adversely affect in a 1. Methodology Section rulemaking with model firm sales and material way the economy, a sector of To estimate the cost, economic either net profit or product value. The the economy, productivity, competition, impacts to potentially affected firms and Agency has also considered the ability jobs, the environment, public health or benefits to society from this proposed of potentially affected firms to pass safety, or State, local, or tribal rulemaking, We evaluated § 3007 compliance costs on in the form of governments or communities; (2) create Survey responses from inorganic higher prices. a serious inconsistency or otherwise chemical producers, firm financial To estimate the benefits of today’s interfere with an action taken or reports, and chemical production data. proposal, we evaluated risk assessment planned by another agency; (3) The Agency has developed model results and as well as a qualitative materially alter the budgetary impact of facilities that represent composite assessment of benefits including natural entitlements, grants, user fees, or loan information about inorganic chemical resource protection of groundwater. programs or the rights and obligations of producers at both the facility and firm recipients thereof; or (4) raise novel, level. We also evaluated two scenarios. 2. Results legal or policy issues arising out of legal The first scenario evaluates the cost of a. Volume Results. Data reviewed by mandates, the President’s priorities, or listing all wastes that we propose to list the Agency indicates that there are 9 the principles set forth in the Executive in today’s proposal. The second inorganic chemical producers Order. scenario includes not only wastes that potentially affected by today’s proposed The Agency estimated the costs of EPA has proposed to list but also any rule. The data report that these firms today’s proposed rule to determine if it waste that has exceeded risk screens (or generated 700,000 tons of inorganic is a significant regulation as defined by other screening criteria) and had chemical production waste annually the Executive Order. The analysis quantitative risk assessment completed. that are potentially affected by today’s considered compliance costs and Analysis of these scenarios allows the proposed rule and modeled under economic impacts for inorganic public to understand what costs would Scenario 1. Data also indicate that there chemical producers affected by this have resulted from this rule making if rule. We estimate the total cost of the all of the quantitative risk assessments are 26 inorganic chemical producers rule to be $3 million annually. This involving fate and transport modeling who have generated wastes that are analysis suggests that this rule is not had shown risk to human health. either being listed because they exhibit economically significant according to To estimate the incremental cost of a characteristic or have been evaluated the definition in E.O. 12866. The Office this rule making, we reviewed baseline for quantitative risk assessment of Management and Budget has deemed management practices and costs of involving fate and transport modeling this rule to be significant for novel potentially affected firms. Where more by the Agency to evaluate their potential policy reasons and has reviewed this than one baseline management method effect on human health and the rule. was used (e.g. municipal incineration environment. These wastes are being Detailed discussions of the and landfilling), we either modeled modeled under Scenario 2. methodology used for estimating the more than one form of baseline b. Cost Results. For today’s proposed costs, economic impacts and the management or selected the least rule, we estimate the total annual benefits attributable to today’s proposed expensive form of baseline management incremental costs from today’s proposal rule for listing hazardous wastes from (which would overestimate rather than to be $ 2.5 million for all facilities. inorganic chemical production, underestimate the cost of the rule). Sectors costs are summarized in Table 2.

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TABLE VIII±1.ÐESTIMATED INCREMENTAL COST BY INORGANIC CHEMICAL SECTOR

Estimated incremental annual costs Number of affected $ 000s facilities Sector (1999 $) Scenario 1 Scenario 2 Scenario 1 Scenario 2

Antimony Oxide ...... 1.6 (recycling), 1.6 (recycling), 33 35 (disposal). 35 (disposal). Hydrogen Cyanide ...... 215 ...... 3 5 Sodium Chlorate ...... 225 ...... 0 5 Sodium Phosphate ...... 76 ...... 0 4 Titanium Dioxide ...... 2900 ...... 6500 ...... 3 9 Total ...... 2937 ...... 7051 ...... 9 26

c. Economic Impact Results. To and comment rulemaking requirements in the potential impacts of the proposed estimate potential economic impacts under the Administrative Procedures rule on small entities and welcome resulting from today’s proposed rule, we Act or any other statute unless the comments on issues related to such used first order economic impacts agency certifies that the rule will not impacts. measures such as the estimated have a significant economic impact on C. Paperwork Reduction Act incremental costs of today’s proposed a substantial number of small entities. rule as a percentage of both affected Small entities include small businesses, The information collection firms’ sales and estimated profits 64. We small organizations, and small requirements in this proposed rule have applied these measures to affected governmental jurisdictions. been submitted for approval to the inorganic chemical producers. For For purposes of assessing the impacts Office of Management and Budget affected inorganic chemical producers of today’s rule on small entities, a small (OMB) under the Paperwork Reduction in the antimony oxide and sodium entity is defined as: (1) A small business Act, 44 U.S.C. 3501 et seq. An chlorate sectors, we estimated the costs that has fewer than 1000 or 100 Information Collection Request (ICR) to be less than 3 percent of a typical employees per firm depending upon the document has been prepared (ICR No. firm’s sales and less than 2 percent of SIC code the firm primarily classified 1968.01) and a copy may be obtained a firm’s estimated profits. For affected in 65; (2) a small governmental from Sandy Farmer by mail at inorganic chemical producers in the jurisdiction that is a government of a Collection Strategies Division; U.S. hydrogen cyanide sector, we estimated city, county, town, school district or Environmental Protection Agency the cost to be less than 1 percent of a special district with a population of less (2822); 1200 Pennsylvania Ave., NW, typical firm’s sales and estimated than 50,000; and (3) a small Washington, DC 20460,by email at profits. More detailed information on organization that is any not-for-profit [email protected], or by this estimate can be found in the enterprise which is independently calling (202) 260–2740. A copy may also economic analysis placed into today’s owned and operated and is not be downloaded off the internet at http:/ docket. dominant in its field. /www.epa.gov/icr. d. Benefits Assessment. EPA has not After considering the economic This rule is proposed under the conducted a quantitative assessment of impacts of today’s proposed rule on authority of sections 3001(e)(2) and actual benefits from this proposed rule. small entities, I certify that this action 3001(b)(1) of the Hazardous and Solid Because today’s proposed rule results in will not have a significant economic Waste Amendments (HSWA) of 1984. new hazardous waste management impact on a substantial number of small The effect of listing the wastes described requirements for K176, K177, and K178 entities. earlier will be to subject industry to wastes, the Agency believes that there There are two potentially affected management and treatment standards inorganic producing firms that may be a reduction in releases of under the Resource Conservation and constitute small entities. These firms are hazardous constituents to the Recovery Act (RCRA). located in the antimony oxide sector. environment. This proposed rule does not contain We have determined that these two any new information collection B. Regulatory Flexibility Act (RFA), as firms would under this proposal incur requirements, nor does it propose to amended by the Small Business costs of less than 1 percent of both the modify any existing information Regulatory Enforcement Fairness Act of firm’s sales and estimated profits under collection requirements. As a result, this 1996 (SBREFA), 5 USC 601 et. seq. one scenario analyzed for the wastes in proposed rule represents only an The RFA generally requires an agency this sector. We continue to be interested incremental increase in burden for to prepare a regulatory flexibility generators and subsequent handlers of 65 The Small Business Administration has analysis of any rule subject to notice classified firms in the manufacturing sector (SIC the newly listed wastes in complying Codes 20–39) and wholesale trade sector (SIC Codes with existing RCRA information 64 Because profit information is often either 50–51) as small businesses within the sector based collection requirements. unavailable or more variable from year to year than on the number of employees per firm. See Small The total annual respondent burden sales measures, the Agency has chose to use a profit Business Size Standards, 61 FR 3280, 3289 (January surrogate in completing the economic impact 31, 1996). Thus, to determine if a inorganic and cost for all existing paperwork analysis of this proposal. According to Dun and chemical producer is a small business, the primary associated with this proposed rule Bradstreet’s Industry Norms and Key Business SIC code of the firm would have to be determined. presented here represents the Indicators (1995) the average net after tax profit for The small entities in today’s rulemaking are in two incremental increase in paperwork inorganic chemical producers in the 2819 SIC code SIC codes: (1) 2812 Alkalies and Chlorine, size was 6.3 percent. This percentage is applied to standard 1000 employees and (2) 5082 Construction burden under six existing Information reported sales of affected firms in order to estimate and Mining (except Petroleum) Machinery and Collection Requests (ICRs). We estimate their profits. Equipment size standard 100 employees. the total annual respondent burden for

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The plan must proposed, and to benefit all populations. approximately 417 hours, at an annual provide for notifying potentially As such, this rule is not expected to cost of approximately $19,916. affected small governments, enabling cause any disproportionately high and Comments are requested on the officials of affected small governments adverse impacts to minority or low- Agency’s need for this information, the to have meaningful and timely input in income communities versus non- accuracy of the provided burden the development of EPA regulatory minority or affluent communities. estimates, and any suggested methods proposals with significant Federal In making hazardous waste listing for minimizing respondent burden, intergovernmental mandates, and determinations, we base our evaluations including through the use of automated informing, educating, and advising of potential risk from the generation and collection techniques. Send comments small governments on compliance with management of solid wastes on an on the ICR to the Director, Collection the regulatory requirements. analysis of potential individual risk. In Strategies Division; U.S. Environmental Today’s rule contains no Federal conducting risk evaluations, our goal is Protection Agency (2822); 1200 mandates (under the regulatory to estimate potential risk to any Pennsylvania Ave., NW, Washington, provisions of Title II of the UMRA) for population of potentially exposed DC 20460; and to the Office of State, local, or tribal governments or the individuals (e.g., home gardeners, adult Information and Regulatory Affairs, private sector. The rule would not farmers, children of farmers, anglers) Office of Management and Budget, 725 impose any federal intergovernmental located in the vicinity of any generator 17th St., N.W., Washington, DC 20503, mandate because it imposes no or facility handling a waste. Therefore, marked ‘‘Attention: Desk Officer for enforceable duty upon state, tribal or we are not putting poor, rural, or EPA.’’ Include the ICR number in any local governments. States, tribes and minority populations at any correspondence. Since OMB is required local governments would have no disadvantage with regard to our to make a decision concerning the ICR compliance costs under this rule. It is evaluation of risk or with regard to how between 30 and 60 days after September expected that states will adopt similar the Agency makes its proposed 14, 2000, a comment to OMB is best rules, and submit those rules for hazardous waste listing determinations. assured of having its full effect if OMB inclusion in their authorized RCRA In proposing today to list wastes as receives it by October 16, 2000. The programs, but they have no legally hazardous (i.e., filter baghouses and low proposed rule will respond to any OMB enforceable duty to do so. For the same antimony slags from antimony oxide or public comments on the information reasons, we determined that this rule production that are discarded, collection requirements contained in contains no regulatory requirements that nonexempt nonwastewater from the this proposal. might significantly or uniquely affect titanium dioxide chloride-ilmenite small governments. We have fulfilled process,), all populations potentially D. Unfunded Mandates Reform Act the requirement for analysis under the exposed to these wastes or potentially Title II of the Unfunded Mandates Unfunded Mandates Reform Act. exposed to releases of the hazardous Reform Act of 1995 (UMRA), Public constituents in the wastes will benefit Law 104–4, establishes requirements for E. Executive Order 12898: from the proposed listing determination. Federal agencies to assess the effects of Environmental Justice In addition, listing determinations take their regulatory actions on State, local, EPA is committed to addressing effect at the national level. The wastes and tribal governments and the private environmental justice concerns and is proposed to be listed as hazardous will sector. Under section 202 of the UMRA, assuming a leadership role in be hazardous regardless of where they EPA generally must prepare a written environmental justice initiatives to are generated and regardless of where statement, including a cost-benefit enhance environmental quality for all they may be managed. Although the analysis, for proposed and final rules populations in the United States. The Agency understands that the proposed with ‘‘Federal mandates’’ that may Agency’s goals are to ensure that no listing determinations, if finalized, may result in expenditures to State, local, segment of the population, regardless of affect where these wastes are managed and tribal governments, in the aggregate, race, color, national origin, or income in the future (in that hazardous wastes or to the private sector, of $100 million bears disproportionately high and must be managed at subtitle C facilities), or more in any one year. Before adverse human health or environmental the Agency’s decision to list these promulgating an EPA rule for which a impacts as a result of EPA’s policies, wastes as hazardous is independent of written statement is needed, section 205 programs, and activities, and that all any decisions regarding the location of of the UMRA generally requires EPA to people live in safe and healthful waste generators and the siting of waste identify and consider a reasonable environments. In response to Executive management facilities. number of regulatory alternatives and Order 12898 and to concerns voiced by Similarly, in cases where the Agency adopt the least costly, most cost- many groups outside the Agency, EPA’s is proposing not list a solid waste as effective or least burdensome alternative Office of Solid Waste and Emergency hazardous because the waste does not that achieves the objectives of the rule. Response formed an Environmental meet the criteria for being identified as The provisions of section 205 do not Justice Task Force to analyze the array a hazardous waste, these decisions are apply when they are inconsistent with of environmental justice issues specific based upon an evaluation of potential applicable law. Moreover, section 205 to waste programs and to develop an individual risks located in proximity to allows EPA to adopt an alternative other overall strategy to identify and address any facility handling the waste. than the least costly, most cost-effective these issues (OSWER Directive No. Therefore, any population living or least burdensome alternative if the 9200.3–17). proximately to a facility that produces a Administrator publishes with the Today’s proposed rule covers wastes solid waste that the Agency has proposed rule an explanation why that from inorganic chemical production. It proposed not to list would not be alternative was not adopted. Before EPA is not certain whether the adversely affected either because the establishes any regulatory requirements environmental problems addressed by waste is already being managed as a that may significantly or uniquely affect this rule could disproportionately affect hazardous waste in the Subtitle C small governments, including tribal minority or low-income communities. system or because the solid waste does governments, it must have developed Today’s proposed rule is intended to not pose a sufficient risk to the local under section 203 of the UMRA a small reduce risks of hazardous wastes as population. We encourage all

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We the Executive Order to include on facilities that have evaluated considered risks to children in our risk regulations that have ‘‘substantial direct potential ecological and human health assessment. The more appropriate and effects on the States, on the relationship impacts (taking into account subsistence safer management practices proposed in between the national government and patterns and sensitive populations) to this rule are projected to reduce risks to the States, or on the distribution of minority or low-income communities. children potentially exposed to the power and responsibilities among the constituents of concern. The public is various levels of government.’’ F. Executive Order 13045: Protection of invited to submit or identify peer- Under Section 6 of Executive Order Children From Environmental Health reviewed studies and data, of which the 13132, EPA may not issue a regulation Risks and Safety Risks agency may not be aware, that assess that has federalism implications, that Executive Order 13045, ‘‘Protection of results of early life exposure to the imposes substantial direct compliance Children from Environmental Health proposed hazardous constituents from costs, and that is not required by statute, Risks and Safety Risks’’ (62 FR 19885, wastes from inorganic chemical unless the Federal government provides April 23, 1997), applies to any rule that: production proposed for listing in the funds necessary to pay the direct (1) is determined to be ‘‘economically today’s rulemaking. compliance costs incurred by State and significant’’ as defined under Executive local governments, or EPA consults with G. Executive Order 13084: Consultation Order 12866, and (2) concerns an State and local officials early in the and Coordination With Indian Tribal environmental health or safety risk that process of developing the proposed Governments EPA has reason to believe may have a regulation. EPA also may not issue a disproportionate effect on children. If Under Executive Order 13084, EPA regulation that has federalism the regulatory action meets both criteria, may not issue a regulation that is not implications and that preempts State the Agency must evaluate the required by statute, that significantly or law, unless the Agency consults with environmental health or safety effects of uniquely affects the communities of State and local officials early in the the planned rule on children, and Indian tribal governments, and that process of developing the proposed explain why the planned regulation is imposes substantial direct compliance regulation. preferable to other potentially effective costs on those communities, unless the Section 4 of the Executive Order and reasonably feasible alternatives Federal government provides the funds contains additional requirements for considered by the Agency. This necessary to pay the direct compliance rules that preempt State or local law, proposed rule is not subject to the costs incurred by the tribal even if those rules do not have Executive Order because it is not governments, or EPA consults with federalism implications (i.e., the rules economically significant as defined in those governments. If EPA complies by will not have substantial direct effects E.O. 12866, and because the Agency consulting, Executive Order 13084 on the States, on the relationship does not have reason to believe the requires EPA to provide to the Office of between the national government and environmental health or safety risks Management and Budget, in a separately the states, or on the distribution of addressed by this action present a identified section of the preamble to the power and responsibilities among the disproportionate risk to children. rule, a description of the extent of EPA’s various levels of government). Those The topic of environmental threats to prior consultation with representatives requirements include providing all children’s health is growing in of affected tribal governments, a affected State and local officials notice regulatory importance as scientists, summary of the nature of their concerns, and an opportunity for appropriate policy makers, and village leaders and a statement supporting the need to participation in the development of the continue to recognize the extent to issue the regulation. In addition, regulation. If the preemption is not which children are particularly Executive Order 13084 requires EPA to based on express or implied statutory vulnerable to environmental hazards. develop an effective process permitting authority, EPA also must consult, to the Recent EPA actions have been in the elected officials and other extent practicable, with appropriate forefront of addressing environmental representatives of Indian tribal State and local officials regarding the threats to the health and safety of governments ‘‘to provide meaningful conflict between State law and children. Today’s proposed rule further and timely input in the development of Federally protected interests within the reflects our commitment to mitigating regulatory policies on matters that agency’s area of regulatory environmental threats to children. significantly or uniquely affect their responsibility. A few significant physiological communities.’’ This proposed rule does not have characteristics are largely responsible For the reasons described above, federalism implications. It will not have for children’s increased susceptibility to today’s proposed rule does not create a substantial direct effects on the States, environmental hazards. First, children mandate on State, local or tribal on the relationship between the national eat proportionately more food, drink governments, nor does it impose any government and the States, or on the proportionately more fluids, and breathe enforceable duties on these entities. distribution of power and more air per pound of body weight than Accordingly, the requirements of responsibilities among the various do adults. As a result, children section 3(b) of Executive Order 13084 levels of government, as specified in potentially experience greater levels of do not apply to this rule. Executive Order 13132. This proposed exposure to environmental threats than rule directly affects primarily inorganic do adults. Second, because children’s H. Executive Order 13132—Federalism chemical producers. There are no State bodies are still in the process of Executive Order 13132, entitled and local government bodies that incur development, their immune systems, ‘‘Federalism’’ (64 FR 43255, August 10, direct compliance costs by this neurological systems, and other 1999), requires EPA to develop an rulemaking. State and local government

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The This proposed rule would preempt performance level for leachability is Environmental protection, Air State and local law that is less stringent based on the Best Commercially- pollution control, Chemicals, for these inorganic chemical production Available Demonstrated Technology Emergency Planning and Community wastes as hazardous wastes. Under the (BDAT). The use of the TCLP for the Right-to-Know Act, Extremely Resource Conservation and Recovery same constituents assures uniformity hazardous substances, Hazardous Act (RCRA), 42 U.S.C. 6901 to 6992k, and consistency in the treatment of chemicals, Hazardous materials, the relationship between the States and hazardous waste in fulfillment of the Hazardous materials transportation, the national government with respect to Congressional Mandate to minimize Hazardous substances, Hazardous hazardous waste management is long-term threats to human health or the wastes, Intergovernmental relations, established for authorized State environment. 42 U.S.C. 6924(m). The Natural resources, Reporting and hazardous waste programs, 42 U.S.C. use of any voluntary consensus standard recordkeeping requirements, Superfund, 6926 (3006), and retention of State would be impractical with applicable Waste treatment and disposal, Water authority, 42 U.S.C. 6929 (3009). Under law because it would require a different pollution control, Water supply. section 3009 of RCRA, States and their leaching method than is currently used Dated: August 30, 2000. political subdivisions may not impose to determine hazardous characteristics. Carol M. Browner, requirements less stringent for The use of different chemical methods hazardous waste management than the to assess hazardousness of the waste Administrator. national government. By publishing and and compliance with treatment For the reasons set forth in the inviting comment on this proposed rule, standards would create disparate results preamble, title 40, chapter I of the Code we hereby provide State and local between hazardous waste identification of Federal Regulations is proposed to be officials notice and an opportunity for and effective treatment of land disposed amended as follows: appropriate participation. Thus, we hazardous wastes. We have not, PART 148ÐHAZARDOUS WASTE have complied with the requirements of therefore, used any voluntary consensus INJECTION RESTRICTIONS section 4 of the Executive Order. standards. EPA welcomes comments on I. National Technology Transfer and this aspect of the proposed rulemaking 1. The authority citation for Part 148 Advancement Act and, specifically, invites the public to continues to read as follows: identify potentially-applicable Section 12(d) of the National Authority: Secs. 3004, Resource voluntary consensus standards and to Conservation and Recovery Act, 42 U.S.C. Technology Transfer and Advancement explain why such standards should be 6901 et seq. Act of 1995 (‘‘NTTAA’’), Public Law used in this regulation. EPA has also 104–113, section 12(d) (15 U.S.C. 272 issued an advanced notice of proposed 2. Section 148.18 is amended by note) directs EPA to use voluntary rulemaking for the Land Disposal adding paragraphs (l) and (m) to read as consensus standards in its regulatory Restriction program (65 FR 37932, June follows: activities, unless to do so would be 19, 2000) that has included discussion § 148.19 Waste-specific prohibitions newly inconsistent with applicable law or on the effectiveness of stabilization on listed and identified wastes. otherwise impractical. Voluntary metals in hazardous wastes. consensus standards are technical * * * * * (l) Effective [date six months after standards (e.g., materials specifications, List of Subjects publication of final rule], the wastes test methods, sampling procedures, and 40 CFR Part 148 specified in 40 CFR 261.32 as EPA business practices) that are developed or Hazardous Waste Numbers K176, K177, adopted by voluntary consensus Environmental protection, standards bodies. The NTTAA directs Administrative practice and procedure, and K178 are prohibited from EPA to provide Congress, through OMB, Hazardous waste, Reporting and underground injection. (m) The requirements of paragraphs explanations when the Agency decides recordkeeping requirements, Water (a) through (l) of this section do not not to use available and applicable supply. apply: voluntary consensus standards. This 40 CFR Part 261 (1) If the wastes meet or are treated to proposed rulemaking involves technical Environmental protection, Hazardous meet the applicable standards specified standards. EPA proposes to use Toxicity materials, Waste treatment and disposal, in subpart D of part 268 of this chapter; Characteristic Leaching Procedure Recycling. or (TCLP) for treatment standards for (2) If an exemption from a prohibition associated with hazardous metal 40 CFR Part 268 has been granted in response to a constituents in wastes proposed for Environmental protection, Hazardous petition under subpart C of this part; or listing in today’s proposal. The TCLP is materials, Waste management, (3) During the period of extension of the standard test method used to Reporting and recordkeeping the applicable effective date, if an evaluate the toxicity characteristic for requirements, Land Disposal extension has been granted under the definition of hazardous waste (see Restrictions, Treatment Standards. § 148.4. 40 CFR 261.24) and treatment standards 40 CFR Part 271 for metal constituents under the Land PART 261ÐIDENTIFICATION AND Disposal Restrictions (see 40 CFR 268.40 Environmental protection, LISTING OF HAZARDOUS WASTE Administrative practice and procedure, 66 For more information, please refer to Appendix Confidential business information, 3. The authority citation for Part 261 C of the background document ‘‘Economic Analysis Hazardous material transportation, continues to read as follows: of the Proposed Rule For Listing Hazardous Waste From Inorganic Chemical Production,’’ which was Hazardous waste, Indians-lands, Authority: 42 U.S.C. 6905, 6912(a), 6921, placed in the docket for today’s proposed rule. Intergovernmental relations, Penalties, 6922, 6924(y), and 6938.

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4. Section 261.4 is amended by (iii) The leachate or gas condensate do impoundment is used to temporarily revising paragraph (b)(15) to read as not exhibit any characteristic of store leachate or gas condensate in follows: hazardous waste nor are derived from response to an emergency situation (e.g., any other listed hazardous waste; shutdown of wastewater treatment § 261.4 Exclusions. (iv) Discharge of the leachate or gas system), provided the impoundment has * * * * * condensate, including leachate or gas a double liner, and provided the (b) * * * condensate transferred from the landfill leachate or gas condensate is removed (15) Leachate or gas condensate to a POTW by truck, rail, or dedicated from the impoundment and continues to collected from landfills where certain pipe, is subject to regulation under be managed in compliance with the solid wastes have been disposed, Sections 307(b) or 402 of the Clean conditions of paragraph (b)(15)(v) after provided that: Water Act. the emergency ends. (v) After February 13, 2001, leachate (i) The solid wastes disposed would or gas condensate derived from K169– * * * * * meet one or more of the listing K172 will no longer be exempt if it is 5. In § 261.32, the table is amended by descriptions for Hazardous Waste Codes stored or managed in a surface adding in alphanumeric order (by the K169, K170, K171, K172, K174, K175, impoundment prior to discharge. After first column) the following K176, K177, and K178, if these wastes [date 24 months after publication date of wastestreams to the subgroup had been generated after the effective the final rule], leachate or gas ‘‘Inorganic Chemicals’’ to read as date of the listing; condensate derived from K176, K177, follows: (ii) The solid wastes described in and K178 will no longer be exempt if it paragraph (b)(15)(i) of this section were is stored or managed in a surface § 261.32 Hazardous waste from specific disposed prior to the effective date of impoundment prior to discharge. There sources. the listing: is one exception: if the surface * * * * *

Industry and EPA haz- Hazardous ardous waste No. Hazardous waste code

******* Inorganic chemicals:

******* K176 ...... Baghouse filters from the production of antimony oxide ...... (E) K177 ...... Slag from the production of antimony oxide that is disposed of or speculatively accumulated ...... (T) K178 ...... Nonwastewaters from the production of titanium dioxide by the chloride-ilmenite process. [This listing (T) does not apply to chloride process waste solids from titanium tetrachloride production exempt under section 261.4(b)(7)].

*******

* * * * * APPENDIX VII TO PART 261ÐBASIS * * * * * 6. Appendix VII to Part 261 is FOR LISTING HAZARDOUS WASTE 7. Appendix VIII to Part 261 is amended by adding the following amended by adding in alphabetical wastestreams in alphanumeric order (by EPA hazardous Hazardous constituents for sequence of common name the waste No. which listed the first column) to read as follows: following entries:

***** K176 ...... Arsenic, lead. K177 ...... Antimony. K178 ...... Manganese, thallium.

APPENDIX VIII TO PART 261ÐHAZARDOUS CONSTITUENTS

Chemical Common name Chemical abstracts name abstracts Hazardous No. waste No.

******* Manganese ...... Same ...... 7439±96±5 ......

*******

PART 268ÐLAND DISPOSAL Authority: 42 U.S.C. 6905, 6912(a), 6921, Subpart CÐProhibitions on Land RESTRICTIONS and 6924. Disposal

8. The authority citation for Part 268 9. Section 268.36 is added to read as continues to read as follows: follows:

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§ 268.36 Waste specific prohibitionsÐ to those wastes and units covered by the depending on whether the treatment inorganic chemical wastes. petition; standards are expressed as (a) Effective [date six months from (3) The wastes meet the applicable concentrations in the waste extract or date of publication of final rule], the treatment standards established the waste, or the generator may use wastes specified in 40 CFR Part 261 as pursuant to a petition granted under knowledge of the waste. If the waste EPA Hazardous Wastes Numbers K176, § 268.44; contains regulated constituents in K177, and K178, and soil and debris (4) Hazardous debris has met the excess of the applicable Subpart D treatment standards in § 268.40 or the contaminated with these wastes, levels, the waste is prohibited from land radioactive wastes mixed with these alternative treatment standards in disposal, and all requirements of Part wastes, and soil and debris § 268.45; or 268 are applicable, except as otherwise contaminated with radioactive wastes (5) Persons have been granted an mixed with these wastes are prohibited extension to the effective date of a specified. from land disposal. prohibition pursuant to § 268.5, with 10. In § 268.40, the Table is amended (b) The requirements of paragraph (a) respect to these wastes covered by the by adding in alphanumeric order new of this section do not apply if: extension. entries for K176, K177, and K178 to read (1) The wastes meet the applicable (c) To determine whether a hazardous as follows: treatment standards specified in Subpart waste identified in this section exceeds D of this Part; the applicable treatment standards § 268.40 Applicability of treatment (2) Persons have been granted an specified in § 268.40, the initial standards. exemption from a prohibition pursuant generator must test a sample of the * * * * * to a petition under § 268.6, with respect waste extract or the entire waste,

TREATMENT STANDARDS FOR HAZARDOUS WASTES [Note: NA means not applicable]

Regulated hazardous constituent Wastewaters Nonwastewaters

Waste Waste description and treat- Concentration in mg/ Concentration in mg/ code ment/regulatory subcategory 1 kg5 unless noted as Common name CAS 2 number L3, or technology 4 ``mg/L TCLP'', or code technology code

******* K176 ...... Baghouse filters from the pro- Antimony ...... 7440±36±0 1.9 ...... 1.15 mg/L TCLP duction of antimony oxide. Arsenic ...... 7440±38±2 1.4 ...... 5.0 mg/L TCLP Cadmium ...... 7440±43±9 0.69 ...... 0.11 mg/L TCLP Lead ...... 7439±92±1 0.69 ...... 0.75 mg/L TCLP Mercury ...... 7439±97±6 0.15 ...... 0.025 mg/L TCLP K177 ...... Slag from the production of an- Antimony ...... 7440±36±0 1.9 ...... 1.15 mg/L TCLP timony oxide that is dis- Arsenic ...... 7440±38±2 1.4 ...... 5.0 mg/L TCLP posed of or speculatively ac- Lead ...... 7439±92±1 0.60 ...... 0.75 mg/L TCLP cumulated. K178 ...... Nonwastewaters from the pro- 1,2,3,4,6,7,8- 35822±39±4 0.000035 or CMBST11 0.0025 or CMBST11 duction of titanium dioxide Heptachlorodibenzo-p-dioxin 67562±39±4 0.000035 or CMBST11 0.0025 or CMBST11 by the chloride-ilmenite proc- (1,2,3,4,6,7,8-HpCDD). 0.0025 or CMBST11 ess. [This listing does not 1,2,3,4,6,7,8- apply to chloride process Heptachlorodibenzofuran waste solids from titanium (1,2,3,4,6,7,8-HpCDF). tetrachloride production ex- empt under section 261.4(b)(7).]. 1,2,3,4,7,8,9- 55673±89±7 0.000035 or CMBST11 0.0025 or CMBST11 Heptachlorodibenzofuran (1,2,3,4,7,8,9-HpCDF). HxCDDs (All 34465±46±8 0.000063 or CMBST11 0.001 or CMBST11 Hexachlorodibenzo-p- dioxins). HxCDFs (All 55684±94±1 0.000063 or CMBST11 0.001 or CMBST11 Hexachlorodibenzofurans). 1,2,3,4,6,7,8,9- 3268±87±9 0.000063 or CMBST11 0.005 or CMBST11 Octachlorodibenzo-p-dioxin (OCDD). 1,2,3,4,6,7,8,9- 39001±02±0 0.000063 or CMBST11 0.005 or CMBST11 Octachlorodibenzofuran (OCDF). PeCDDs (All 36088±22±9 0.000063 or CMBST11 0.001 or CMBST11 Pentachlorodibenzo-p- dioxins). PeCDFs (All 30402±15±4 0.000035 or CMBST11 0.001 or CMBST11 Pentachlorodibenzofurans). TCDDs (All tetrachlorodibenzo- 41903±57±5 0.000063 or CMBST11 0.001 or CMBST11 p-dioxins). TCDFs (All 55722±27±5 0.000063 or CMBST11 0.001 or CMBST11 tetrachlorodibenzofurans).

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TREATMENT STANDARDS FOR HAZARDOUS WASTESÐContinued [Note: NA means not applicable]

Regulated hazardous constituent Wastewaters Nonwastewaters

Waste Waste description and treat- Concentration in mg/ Concentration in mg/ code ment/regulatory subcategory 1 kg5 unless noted as Common name CAS 2 number L3, or technology 4 ``mg/L TCLP'', or code technology code

Manganese ...... 7439±96±5 17.1 ...... 3.6 mg/L TCLP Thallium ...... 7440±28±0 1.4 ...... 0.20 mg/L TCLP ******* ******* FOOTNOTES TO TREATMENT STANDARD TABLE 268.40 1 The waste descriptions provided in this table do not replace waste descriptions in 40 CFR part 261. Descriptions of Treatment/Regulatory Subcategories are provided, as needed, to distinguish between applicability of different standards. 2 CAS means Chemical Abstract Services. When the waste code and/or regulated constituents are described as a combination of a chemical with its salts and/or esters, the CAS number is given for the parent compound only. 3 Concentration standards for wastewaters are expressed in mg/L and are based on analysis of composite samples. 4 All treatment standards expressed as a Technology Code or combination of Technology Codes are explained in detail in 40 CFR 268.42 Table 1ÐTechnology Codes and Descriptions of Technology-Based Standards. 5 Except for Metals (EP or TCLP) and Cyanides (Total and Amenable) the nonwastewater treatment standards expressed as a concentration were established, in part, based upon incineration in units operated in accordance with the technical requirements of 40 CFR part 264, Subpart O or 40 CFR part 265, Subpart O, or based upon combustion in fuel substitution units operating in accordance with applicable technical require- ments. A facility may comply with these treatment standards according to provisions in 40 CFR 268.40(d). All concentration standards for nonwastewaters are based on analysis of grab samples. ******* 11 For these wastes, the definition of CMBST is limited to: (1) combustion units operating under 40 CFR 266, (2) combustion units permitted under 40 CFR part 264, Subpart O, or (3) combustion units operating under 40 CFR 265, Subpart O, which have obtained a determination of equivalent treatment under 268.42(b).

11. In § 268.48, the Table is amended a new entry to read as follows: (The § 268.48 Universal treatment standards. by adding in alphabetical order under footnotes are republished without * * * * * the heading of ‘‘Inorganic Constituents’’ change.)

UNIVERSAL TREATMENT STANDARDS [Note: NA means not applicable]

Wastewater Nonwastewater standard standard

Regulated Constituent common name CAS 1 number Concentration in Concentration mg/kg 3 unless in mg/l 2 noted as ``mg/l TCLP'

******* Inorganic Constituents ******* Manganese 7439±96±5 17.1 3.6 mg/l TCLP ******* ******* 1 CAS means Chemical Abstract Services. When the waste code and/or regulated constituents are described as a combination of a chemical with its salts and/or esters, the CAS number is given for the parent compound only. 2 Concentration standards for wastewaters are expressed in mg/L and are based on analysis of composite samples. 3 Except for Metals (EP or TCLP) and Cyanides (Total and Amenable) the nonwastewater treatment standards expressed as a concentration were established, in part, based upon incineration in units operated in accordance with the technical requirements of 40 CFR Part 264, Subpart O, or Part 265, Subpart O, or based upon combustion in fuel substitution units operating in accordance with applicable technical requirements. A facility may comply with these treatment standards according to provisions in 40 CFR 268.40(d). All concentration standards for nonwastewaters are based on analysis of grab samples.

* * * * * Authority: 42 U.S.C. 6905, 6912(a), and § 271.1 Purpose and scope. 6926. * * * * * PART 271ÐREQUIREMENTS FOR AUTHORIZATION OF STATE 13. Section 271.1(j) is amended by (j) * * * HAZARDOUS WASTE PROGRAMS adding the following entries to Table 1 and Table 2 in chronological order by 12. The authority citation for Part 271 date of publication to read as follows. continues to read as follows:

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TABLE 1.ÐREGULATIONS IMPLEMENTING THE HAZARDOUS AND SOLID WASTE AMENDMENTS OF 1984

Promulgation date Title of regulation Federal Register reference Effective date

******* [insert date of signature of final Listing of Hazardous Wastes [insert Federal Register page [insert effective date of final rule] rule] K176, K177, and K178 numbers] *******

TABLE 2.ÐSELF-IMPLEMENTING PROVISIONS OF THE SOLID WASTE AMENDMENTS OF 1984

Effective date Self-implementing provision RCRA citation Federal Register reference

******* [effective date of final rule]. Prohibition on land disposal of 3004(g)(4)(C) and 3004(m). [date of publication of final rule] K176, K177, and K178 wastes, [FR page numbers]. and prohibition on land disposal of mixed with K176, K177, and K178 wastes, including soil and debris. *******

PART 302ÐDESIGNATION, Authority: 42 U.S.C. 9602, 9603, and 9604; alphanumeric order at the end of the REPORTABLE QUANTITIES, AND 33 U.S.C. 1321 and 1361. table to read as follows: NOTIFICATION 15. In § 302.4, Table 302.4 is amended § 302.4 Designation of hazardous 14. The authority citation for Part 302 by adding the following new entries in substances continues to read as follows: * * * * *

TABLE 302.4.ÐLIST OF HAZARDOUS SUBSTANCES AND REPORTABLE QUANTITIES [Note: All Comments/Notes Are Located at the End of This Table]

Regu- Statutory Final RQ Hazardous substance CASRN latory RCRA syno- RQ Code ² Waste Category Pounds nyms Number (Kg)

******* K176 ...... *1 4 K176 X 1 (0.454) Baghouse filters from the production of antimony oxide. K177 ...... *1 4 K177 X 5,000 (2,270) Slag from the production of antimony oxide. K178 ...... *1 4 K178 X # Nonwastewaters from the production of titanium dioxide by the chloride-ilmenite process. [This listing does not apply to chloride process waste solids from titanium tetra- chloride production exempt under section 261.4(b)(7).]. ² Indicates the statutory source as defined by 1, 2, 3, and 4 below. ******* 4-Indicates that the statutory source for designation of this hazardous substance under CERCLA is RCRA Section 3001. 1* Indicates that the 1-pound RQ is a CERCLA statutory RQ. # The Agency may adjust the statutory RQ for this hazardous substance in a future rulemaking; until then the statutory RQ applies. *******

[FR Doc. 00–22810 Filed 9–13–00; 8:45 am] BILLING CODE 6560±50±U

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