301Serbsf10,616*
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
United States Patent Office Patented Sept
3,000,702 United States Patent Office Patented Sept. 19, 196 2 since potassium fluoride is very soluble. In this case, a 3,000,702 MANUEFACTURE OF SODIUM FLUOR DE double or complex salt is formed in the melt between George L. Cunningham, Burtonsville, Md., assignor to potassium fluoride and the calcium salt and that is slowly W. R. Grace & Co., New York, N.Y., a corporation extracted with water in spite of the great solubility of of Connecticut potassium fluoride in water. The corrosion of the molten No Drawing. Filed May 23, 1958, Ser. No. 737,196 melt is also a considerable problem although suitable 4. Claims. (CI. 23-88) ceramic materials have been discovered for constructing the fusion vessel. This invention relates to a process for the manufac Processes have been devised for the production of so ture of sodium fluoride relatively low in silica content. 10 dium fluoride based on the thermal decomposition of More particularly, this invention relates to a cyclic proc sodium silicofluoride to sodium fluoride and silicon tetra ess whereby sodium fluoride, relatively low in silica con fluoride (U.S. 1,896,697, U.S. 2,588,786, 1,730,915, tent and ammonium chloride, may be manufactured from 2,602,726, and U.S. 1,664,348). These processes are cheap and readily available raw materials. faulty in that relatively high temperatures are required to As manufactured at the present time, technical sodium 15 decompose the sodium silicofluoride and thus it is very fluoride contains 94% to 97% NaF and 1.5% to 5.0% difficult to carry the reaction to completion. -
Ammonium Bifluoride CAS No
Product Safety Summary Ammonium Bifluoride CAS No. 1341-49-7 This Product Safety Summary is intended to provide a general overview of the chemical substance. The information on the summary is basic information and is not intended to provide emergency response information, medical information or treatment information. The summary should not be used to provide in-depth safety and health information. In-depth safety and health information can be found in the Safety Data Sheet (SDS) for the chemical substance. Names • Ammonium bifluoride (ABF) • Ammonium difluoride • Ammonium acid fluoride • Ammonium hydrogen difluoride • Ammonium fluoride compound with hydrogen fluoride (1:1) Product Overview Solvay Fluorides, LLC does not sell ammonium bifluoride directly to consumers. Ammonium bifluoride is used in industrial applications and in other processes where workplace exposures can occur. Ammonium bifluoride (ABF) is used for cleaning and etching of metals before they are further processed. It is used as an oil well acidifier and in the etching of glass or cleaning of brick and ceramics. It may also be used for pH adjustment in industrial textile processing or laundries. ABF is available as a solid or liquid solution (in water). Ammonium bifluoride is a corrosive chemical and contact can severely irritate and burn the skin and eyes causing possible permanent eye damage. Breathing ammonium bifluoride can severely irritate and burn the nose, throat, and lungs, causing nosebleeds, cough, wheezing and shortness of breath. On contact with water or moist skin, ABF can release hydrofluoric acid, a very dangerous acid. Inhalation or ingestion of large amounts of ammonium bifluoride can cause nausea, vomiting and loss of appetite. -
1 Abietic Acid R Abrasive Silica for Polishing DR Acenaphthene M (LC
1 abietic acid R abrasive silica for polishing DR acenaphthene M (LC) acenaphthene quinone R acenaphthylene R acetal (see 1,1-diethoxyethane) acetaldehyde M (FC) acetaldehyde-d (CH3CDO) R acetaldehyde dimethyl acetal CH acetaldoxime R acetamide M (LC) acetamidinium chloride R acetamidoacrylic acid 2- NB acetamidobenzaldehyde p- R acetamidobenzenesulfonyl chloride 4- R acetamidodeoxythioglucopyranose triacetate 2- -2- -1- -β-D- 3,4,6- AB acetamidomethylthiazole 2- -4- PB acetanilide M (LC) acetazolamide R acetdimethylamide see dimethylacetamide, N,N- acethydrazide R acetic acid M (solv) acetic anhydride M (FC) acetmethylamide see methylacetamide, N- acetoacetamide R acetoacetanilide R acetoacetic acid, lithium salt R acetobromoglucose -α-D- NB acetohydroxamic acid R acetoin R acetol (hydroxyacetone) R acetonaphthalide (α)R acetone M (solv) acetone ,A.R. M (solv) acetone-d6 RM acetone cyanohydrin R acetonedicarboxylic acid ,dimethyl ester R acetonedicarboxylic acid -1,3- R acetone dimethyl acetal see dimethoxypropane 2,2- acetonitrile M (solv) acetonitrile-d3 RM acetonylacetone see hexanedione 2,5- acetonylbenzylhydroxycoumarin (3-(α- -4- R acetophenone M (LC) acetophenone oxime R acetophenone trimethylsilyl enol ether see phenyltrimethylsilyl... acetoxyacetone (oxopropyl acetate 2-) R acetoxybenzoic acid 4- DS acetoxynaphthoic acid 6- -2- R 2 acetylacetaldehyde dimethylacetal R acetylacetone (pentanedione -2,4-) M (C) acetylbenzonitrile p- R acetylbiphenyl 4- see phenylacetophenone, p- acetyl bromide M (FC) acetylbromothiophene 2- -5- -
Environmental Protection Agency § 117.3
Environmental Protection Agency § 117.3 (4) Applicability date. This paragraph TABLE 117.3—REPORTABLE QUANTITIES OF (i) is applicable beginning on February HAZARDOUS SUBSTANCES DESIGNATED PUR- 6, 2020. SUANT TO SECTION 311 OF THE CLEAN (j) Process waste water means any WATER ACT—Continued water which, during manufacturing or Cat- RQ in pounds processing, comes into direct contact Material egory (kilograms) with or results from the production or use of any raw material, intermediate Ammonium benzoate ...................... D ...... 5,000 (2,270) Ammonium bicarbonate .................. D ...... 5,000 (2,270) product, finished product, byproduct, Ammonium bichromate ................... A ....... 10 (4.54) or waste product. Ammonium bifluoride ...................... B ....... 100 (45.4) Ammonium bisulfite ......................... D ...... 5,000 (2,270) [44 FR 50776, Aug. 29, 1979, as amended at 58 Ammonium carbamate .................... D ...... 5,000 (2,270) FR 45039, Aug. 25, 1993; 65 FR 30904, May 15, Ammonium carbonate ..................... D ...... 5,000 (2,270) 2000; 80 FR 37112, June 29, 2015; 83 FR 5208, Ammonium chloride ........................ D ...... 5,000 (2,270) Feb. 6, 2018] Ammonium chromate ...................... A ....... 10 (4.54) Ammonium citrate dibasic ............... D ...... 5,000 (2,270) Ammonium fluoborate ..................... D ...... 5,000 (2,270) § 117.2 Abbreviations. Ammonium fluoride ......................... B ....... 100 (45.4) NPDES equals National Pollutant Ammonium hydroxide ..................... C -
The Influences of Fluorides on the Transformation of Α-Alumina Crystals
Ceramics-Silikáty 61 (4), 357-366 (2017) www.ceramics-silikaty.cz doi: 10.13168/cs.2017.0035 THE INFLUENCES OF FLUORIDES ON THE TRANSFORMATION OF α-ALUMINA CRYSTALS #QINGBO TIAN*,**, XIAOJIE YANG***, YUE WANG**, ZHIJIE LV** *Co-innovation Center for Green Building of Shandong Province,, Shandong Jianzhu University, Jinan 250101, P. R. China; **School of Material Science and Engineering, Shandong Jianzhu University, Jinan 250101, P. R. China; ***Shandong Institute for Product Quality Inspection, Jinan 250100, P. R. China #E-mail: [email protected] Submitted June 20, 2017; accepted July 29, 2017 Keywords: α-Al2O3 , Morphology, Platelet-like Al2O3, Fluorides Influence of addition of aluminum fluoride (AlF3) and ammonium fluoride (NH4F) on transformation of α-Al2O3 from boehmite was investigated. Transformation of α-Al2O3 occurred at about 1050°C and 950°C, when boehmite contained AlF3 and NH4F additives respectively, which was 150°C and 300°C lower than that without any additives. The formed α-Al2O3 consisted of clear, hexagonal plate-like particles about 2-3 µm in diameter and 200 nm in thickness. However, the formed hexagonal platelet particles gradually became blunt at edges and decreased in sizes at the higher calcinating temperatures. The transfer of α-Al2O3 morphology was due to the diminution and disappearance of fluorine. The fluoride coated on the surfaces were firstly decomposed and then fluorine entered the lattices of crystals was volatilized. The fluoride with tiny particles attached on the surface had a same chemical bonding of F–Al–O with that in the lattices of crystals. INTRODUCTION ration of ammonium nitrate induced the transformation of intermediate phases to the stable α-Al2O3 structure at The high pure alumina ceramics have attracted a lower temperature. -
Used at Rocky Flats
. TASK 1 REPORT (Rl) IDENTIFICATION OF CHEMICALS AND RADIONUCLIDES USED AT ROCKY FLATS I PROJECT BACKGROUND ChemRisk is conducting a Rocky Flats Toxicologic Review and Dose Reconstruction study for The Colorado Department of Health. The two year study will be completed by the fall of 1992. The ChemRisk study is composed of twelve tasks that represent the first phase of an independent investigation of off-site health risks associated with the operation of the Rocky Flats nuclear weapons plant northwest of Denver. The first eight tasks address the collection of historic information on operations and releases and a detailed dose reconstruction analysis. Tasks 9 through 12 address the compilation of information and communication of the results of the study. Task 1 will involve the creation of an inventory of chemicals and radionuclides that have been present at Rocky Flats. Using this inventory, chemicals and radionuclides of concern will be selected under Task 2, based on such factors as the relative toxicity of the materials, quantities used, how the materials might have been released into the environment, and the likelihood for transport of the materials off-site. An historical activities profile of the plant will be constructed under Task 3. Tasks 4, 5, and 6 will address the identification of where in the facility activities took place, how much of the materials of concern were released to the environment, and where these materials went after the releases. Task 7 addresses historic land-use in the vicinity of the plant and the location of off-site populations potentially affected by releases from Rocky Flats. -
United States Patent Office
United States Patent Office 3,330,620 Patented July 11, 1967 2 3,330,620 aqueous solution is used and this base is selected from METHOD FOR OXEDZNG AMMONUMSULFTE TO AMMONUMSULFATE the group consisting of pyridine, picolines, lutidines, col Angel Vian-Ortino and Vicente Martin-Municio, Madrid, lidines, quinoline, pyridic coal-tar bases, pyridic bases Spain, assignors to Empresa Auxiliar de la Industria, derived from petro-chemical processes, bases containing S.A., Madrid, Spain 5 pyridinic condensed rings and derivatives thereof. No Drawing. Fied Apr. 22, 1963, Ser. No. 274,806 The method of the present invention of converting am Claims priority, application Spain, Apr. 23, 1962, monium sulfite into ammonium sulfate may also be car 276,718 ried out by forming a dispersion of an organic, nitro 15 Claims. (C. 23-119) gen-containing base in an aqueous solution of ammonium 10 sulfate and ammonium sulfite, the organic base being in The present invention relates to a process for the soluble in the aqueous solution and being present in an quantitative oxidation of ammonium sulfite and, more amount equal to between 10% and 80% of the volume particularly, for the oxidation of ammonium sulfite which of the dispersion, passing air through the dispersion while has been formed by absorption of sulfur dioxide in aque the same is maintained at an elevated temperature of be ous ammonia solutions. Thus, the present invention is also 5 tween 40 and 140 C. and at an absolute pressure of be concerned with the recovery of sulfur dioxide from waste tween 1 and 11 atmospheres so as to substantially com gases in the form of ammonium sulfate. -
Application News Multi-Residue Analysis of 18 Regulated Mycotoxins by LC-MS/MS (2) No
LAAN-A-LM-E135 LC-MS/MS Application News Multi-residue analysis of 18 regulated mycotoxins by LC-MS/MS (2) No. C165 Fusarium mycotoxins are a structurally diverse group Materials and Methods of secondary metabolites known to contaminate a Solvent extracts were provided by Concept Life Sciences diverse array of food and feed resulting in a risk for following validated extraction protocols. Samples were human and animal health. European guidance measured using a Nexera UHPLC and the LCMS-8060 legislation has set maximum levels for mycotoxins in triple quadrupole detector (Table 1). To separate out the food and feed to minimize the impact to human and three pairs of regioisomers (3-AcDON/15-AcDON, animal health. The most toxicologically important FB2/FB3, and FA2/FA3) a pentafluorophenyl (PFP) column Fusarium mycotoxins are trichothecenes (including was used and compared against a C18 material. To deoxynivalenol (DON) and T-2 toxin (T-2)), zearalenone enhance signal response a series of mobile phase (ZON) and fumonisin B1 (FB1). additives were considered including ammonium acetate, In this work, a single LC-MS/MS method has been ammonium fluoride, ammonium formate and acetic acid developed for the determination of 18 mycotoxins in food solutions. safety. Limits of quantification were at or below the In this work, ammonium fluoride solution and maximum levels set in the EC/1886/2006 document. The ammonium fluoride with acetic acid solution was the scope of the method included aflatoxins (B1, B2, G1, G2), preferred solvent system as it resulted in a considerable fumonisins (B1, B2, B3), ochratoxin A (OTA) and enhancement of signal intensity in positive ion mode trichothecenes (3-acetyldeoxynivalenol (3-AcDON), 15- for all mycotoxins. -
Control of IL J
By Control of IL J. L. Ricard, T. E. See, and W. B. Bollen Oregon State University Incipient Decay Corvallis, Oreg. With Gases in Douglas-fir Poles t-200 THERMOBAROME TER D WOOD AL NE cr 00°A • 0 z METHYL BROMIDE- ALONE - cr 100 cr) METHYL BROMIDE AND WOOD cc Foreword a. In 1962, Messrs. 0. F. Hand and A. F. Wetsch, of the Bonneville Power Administration, began a study of gas diffusion systems for controlling I - decay fungi and insects in Douglas-fir and West- 10 20 30 40 50 ern Red Cedar utility poles. Many fumigants were MINUTES tested in that year, among them Chlorodane, Figure 1. — Evaluation of Warburg apparatus for study Chloropicrin, Ethylene Dibromidc, Vapam, Tc- of methyl bromide absorption by wood at 1.4°C. The break lone, Cresan M, Cyanogas and Methyl Bromide. in the curve for methyl bromide and wood is attributable Fungi and insects were killed by several of the to resetting the manometer. materials tested as confirmed by bio-assay tech- niques. Reported as among the most effective tested were Vapam, Cyanogas, Chloropicrin, and ERVICE LIFE of Douglas-fir poles could be ex- S Methyl Bromide. Following the work by Bonne- tended if they could be penetrated readily by fungicides with long-lasting effects. Incipient ville Power Administration, a cooperative research contract was established with the Forest Research decay is readily detected in poles (16), and the Overholts, Laboratory, Oregon State University, to evaluate common decay fungus, Poria carbonica chemical treatments for arresting decay in poles. is sensitive to fungicides (15). -
Appendix C: Natural Resources and Environmental Protection
A Appendix C: P Natural Resources P and Environmental E Protection Act (NREPA) Part 31 – N Part 5 Rules D • Applicability Flow Chart I • Part 5 Rules with Notes X C APPENDIX C: NREPA Part 31 – Part 5 Rules Applicability Flow Chart - Part 5 Rules Spillage of Oil and Polluting Materials Review the administrative rules (R 324.2001 – R 324.2009) on the following pages and ask the questions below to determine if the Part 5 requirements apply. Does the facility meet the definition of an oil storage or on-land facility per R 324.2001 (f) or (g)? No Yes Does the facility have polluting materials that all meet the small container exemption or are regulated by (and in compliance with) another Yes Not subject to Part 5 requirements. program listed in R 324.2003 excluding R 324.2003 (1)(b)? No Does the facility have polluting materials in regulated Threshold Management Quantities (TMQs) per R 324.2002 (f)? No Polluting materials include mixtures containing 1% or more, by weight, of any substances listed below. SALT LISTED CHEMICALS OIL R 324.2009 Solid form - 5 tons Single container or tank having 660 gallon storage or Liquid form - 1,000 gallons Outdoors – 440 pounds capacity Indoors – 2,200 pounds Total capacity of 1,320 gallons above ground storage REQUIREMENTS o Pollution Incident Prevention Plan (PIPP) – R 324.2006 REQUIREMENTS Including notification requirements to EGLE , local health o Use Area & Indoor Storage – R 324.2005 department, and local emergency planning committee o Surveillance – R 324.2004 o Secondary Containment – R 324.2005 o -
Effects of Post-Manufacture Board Treatments on Formaldegyde Emission
Effects of post-manufacture board treatments on formaldehyde emission: a literature review (1960-1984) George E. Myers treatments. At present I suggest that impregnation of Abstract boards with aqueous solutions (Method 1) is likely to be This paper reviews the literature dealing with the the most reliable because it should permit the use of a many post-manufacture board treatments used to re large scavenger excess and also allow neutralization of duce formaldehyde emission from urea-formaldehyde board acidity to reduce resin hydrolysis. bonded boards. Such treatments have almost solely used one or more of five chemical or physical principles: 1) formaldehyde reaction with NH3, 2) formaldehyde reaction with oxygenated sulfur compounds, 3) formal This is the fifth in a planned series of six critical dehyde reaction with organic -NH functionality, 4) pH reviews of the literature on different aspects of the adjustment, and 5) physical barrier. I have categorized problem of formaldehyde emission from adhesively the available reports according to four primary board bonded wood products. The series was initiated at the treatment methods that use the five principles in differ Forest Products Laboratory, Madison, Wis., in response ent ways. The four primary treatment methods are: to a need expressed by industry representatives for an 1. Application of scavengers as solids or aqueous independent evaluation and summation of data from solutions. Ammonium bicarbonate and carbonate have diverse sources. The six aspects being reviewed concern been used as solid powders, while the solutions involved the effects of formaldehyde-to-urea mole ratio (F/U) a variety of ammonium salts, ammonium and alkali (48), ventilation rate and loading (49), temperature and metal salts with sulfur-containing anions, and urea and humidity (51), separate additions to wood furnish or other compounds having -NH functionality; veneer (52), post-manufacture treatments of boards, 2. -
Ammonium Fluoride Product Stewardship Summary February 2012
Ammonium Fluoride Product Stewardship Summary February 2012 (NH4)F Chemical Name: Ammonium Fluoride Chemical Category (if applicable): Inorganic neutral halide Synonyms: Neutral ammonium fluoride; Commercial ammonium fluoride; and (NH4)F CAS Number: 12125-01-8 CAS Name: Ammonium fluoride EC (EINECS) Number: 235-185-9 Other identifier (Please specify): GPS0050 Honeywell manufactures ammonium fluoride that is used by industry in the manufacture of electronic materials. Exposure can occur at either an ammonium fluoride manufacturing facility or at other manufacturing, packaging or storage facilities that handle ammonium fluoride. Persons involved in maintenance, sampling and testing activities, or in the loading and unloading of packages containing ammonium fluoride are at risk of exposure, but worker exposure can be controlled with the use of proper general mechanical ventilation and personal protective equipment. Workplace exposure limits for fluoride ion have been established for use in worksite safety programs. When ammonium fluoride is a component of consumer products, users should follow manufacturer’s use and/or label instructions. Ammonium fluoride dusts released to the atmosphere and deposited in soil or surface water in the vicinity of production sites have negligible impact on the environment. Please see the MSDS for additional information. Ammonium fluoride is a nonflammable solid that is stable under normal conditions. Ammonium fluoride is corrosive to metals and glass. It can react with acids to liberate hydrogen fluoride and bases to liberate ammonia. When heated to decomposition, it will release toxic hydrogen fluoride gas and ammonia. Contact of ammonium fluoride with water or extended skin contact under moist conditions can produce hydrofluoric acid (HF), a very dangerous acid that can cause burns of the skin and eyes.