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Vanadium Pentoxide and Other Inorganic Vanadium Compounds
This report contains the collective views of an international group of experts and does not necessarily represent the decisions or the stated policy of the United Nations Environment Programme, the International Labour Organization, or the World Health Organization. Concise International Chemical Assessment Document 29 VANADIUM PENTOXIDE AND OTHER INORGANIC VANADIUM COMPOUNDS Note that the layout and pagination of this pdf file are not identical to the printed CICAD First draft prepared by Dr M. Costigan and Mr R. Cary, Health and Safety Executive, Liverpool, United Kingdom, and Dr S. Dobson, Centre for Ecology and Hydrology, Huntingdon, United Kingdom Published under the joint sponsorship of the United Nations Environment Programme, the International Labour Organization, and the World Health Organization, and produced within the framework of the Inter-Organization Programme for the Sound Management of Chemicals. World Health Organization Geneva, 2001 The International Programme on Chemical Safety (IPCS), established in 1980, is a joint venture of the United Nations Environment Programme (UNEP), the International Labour Organization (ILO), and the World Health Organization (WHO). The overall objectives of the IPCS are to establish the scientific basis for assessment of the risk to human health and the environment from exposure to chemicals, through international peer review processes, as a prerequisite for the promotion of chemical safety, and to provide technical assistance in strengthening national capacities for the sound management -
Phosphate-Based Treatments for Conservation of Stone
RILEM Technical Letters (2017) 2: 14‐19 DOI: http://dx.doi.org/10.21809/rilemtechlett.2017.34 Phosphate‐based treatments for conservation of stone Enrico Sassoni a* a Department of Civil, Chemical, Environmental and Materials Engineering, University of Bologna, Via Terracini 28, 40131, Bologna, Italy Received: 30 May 2017 / Accepted: 09 August 2017 / Published online: 9 October 2017 © The Author(s) 2017. This article is published with open access and licensed under a Creative Commons Attribution 4.0 International License. Abstract To overcome the limitations of currently available protectives and consolidants for carbonate stones (such as marble and limestone), in 2011 the use of calcium phosphate was proposed. The idea is forming calcium phosphates (ideally hydroxyapatite) as the reaction product between the substrate and an aqueous solution of a phosphate salt that the stone is treated with. In this paper, the studies aimed at identifying the best treatment conditions (in terms of nature and concentration of the phosphate precursor, solution pH, reaction time, ionic and organic additions) are first briefly summarized. Then, the efficacy of the phosphate treatment in protecting marble from dissolution in rain and restoring cohesion of weathered marble and limestone is discussed. Some recent studies on the use of the phosphate treatment on alternative substrates and some future steps for research on the topic are finally outlined. Keywords: Cultural heritage; Marble; Hydroxyapatite; Protection; Consolidation 1 Introduction improve mechanical properties, by providing a binding action between the stone grains. Organic products are A great part of cultural heritage objects (e.g. monuments, effective in improving mechanical properties, but again architectural decorations and statues) is made of carbonate they lack compatibility and durability. -
United States Patent (19) 11 Patent Number: 5,883,058 Wells Et Al
USOO5883058A United States Patent (19) 11 Patent Number: 5,883,058 Wells et al. (45) Date of Patent: *Mar 16, 1999 54 HIGH LATHER STYLING SHAMPOOS 4,784,801 11/1988 Hoeffkes et al. ....................... 252/554 5,084.212 1/1992 Farris et al. ............................ 252/554 (75) Inventors: Robert Lee Wells, Cincinnati, Ohio; 5,104,642 4/1992 Wells et al. ..... ... 424/47 Jon Robert Behrens, Kobe, Japan 5,120,532 6/1992 Wells et al. ............ ... 424/70 5,310,508 5/1994 Subramanyam et al. ............... 252/549 73) Assignee: The Procter & Gamble Company, 5,391,368 2/1995 Gerstein ............................... 424/70.13 5,514,302 5/1996 Brown ..................................... 252/545 Cincinnati, Ohio 5,580,494 12/1996 Sandhu et al. .......................... 510/125 Notice: The term of this patent shall not extend FOREIGN PATENT DOCUMENTS beyond the expiration date of Pat. No. 5,672.576. 0323715 12/1989 European Pat. Off.. Appl. No.: 520,631 Primary Examiner Paul Lieberman Assistant Examiner Necholas Ogden Filed: Aug. 29, 1995 Attorney, Agent, or Firm Joan B. Tucker; William J. Int. Cl." ................................................ C110 1/83 Winter; Tara M. Rosnell U.S. Cl. .......................... 510/127; 510/119,510/123; 57 ABSTRACT 510/125; 424/70.11; 424/70.24 The present invention relates to hair shampoo compositions Field of Search ..................................... 252/549, 550, which have improved cleansing, lathering, and Styling ben 252/551, 557; 510/119, 123,125, 127; efits=. These Shampoo compositions comprise an alkyl glyc 424/70.24, 70.11 eryl ether Sulfonate Surfactant, a hair Styling polymer, a 56) References Cited non-polar volatile Solvent, and water. -
Chemistry Inventory; Fall
CHEMISTRY FALL 2005 MSDS Mfg.'s Name Chemical Name Quantity Stored Storage Conditions (on file = 9) Aluminum 9 1.5 kg Aluminum chloride, anhydrous, 98.5% 9 0.2 kg Aluminum chloride · 6H2O 9 0.5 kg Aluminum hydroxide 9 0.5 kg Aluminum nitrate 9 0.5 kg Aluminum sulfate 9 0.5 kg Ammonia, concentrated 9 4.0 L Ammonium acetate 9 0.2 kg Ammonium chloride 9 Ammonium dihydrogen phosphate (monobasic) 9 0.4 kg J.T. Baker Ammonium hydrogen phosphate (dibasic) No 0.5 kg Ammonium nitrate 9 2.5 kg Ammonium oxalate 9 0.7 kg Ammonium peroxydisulfate 9 0.5 kg Ammonium sulfate 9 0.2 kg Antimony 9 0.4 kg Barium chloride, anhydrous 9 2.5 kg Barium chloride · 2H2O 9 2.5 kg Barium nitrate 9 0.8 kg Bismuth 9 2.0 kg Boric Acid 9 0.4 kg Brass 9 Bromine 9 2.5 kg Cadmium 9 0.1 kg Cadmium nitrate 9 0.3 kg Calcium acetate · xH2O 9 0.5 kg Calcium carbide 9 1.0 kg Calcium carbonate 9 2.2 kg Calcium chloride 9 1.0 kg Calcium hydroxide 9 0.3 kg Calcium nitrate · 4H2O 9 1.0 kg Calcium oxide 9 0.3 kg Calcium sulfate · 2H2O 9 1.0 kg Carbon 9 0.1 kg Ceric ammonium nitrate 9 0.5 kg Cesium chloride 9 0.01 kg Chromium 9 0.01 kg Chromium chloride 9 0.5 kg Chromium nitrate 9 0.5 kg Cobalt 9 0.025 kg Cobalt chloride 9 0.7 kg Cobalt nitrate 9 0.6 kg Copper (assorted) 9 4.0 kg Copper acetate 9 0.05 kg Copper chloride 9 0.1 kg Copper nitrate 9 3.5 kg Copper oxide 9 0.4 kg Cupric sulfate, anhydrous 9 0.5 kg Cupric sulfate · 5H2O 9 2.75 kg EDTA 9 0.6 kg Iodine 9 2.0 kg Iron (assorted) 9 5.0 kg MSDS Mfg.'s Name Chemical Name Quantity Stored Storage Conditions (on file = 9) Ferric ammonium -
Gravimetric Determination of Vanadium As V(IV)-Oxinate
Chem. Anal. (Warsaw), 38, 639 (1993) Gravimetric Determination of Vanadium as V(IV)-Oxinate by S. Kaur, A. K. Chhakkarand L. R. Kakkar* Department ofChemistry, Kurukshetra University, Kurukshetra -132119, Haryana; India Key words: vanadium(V), oxine, 8-hydroxyquinoline, gravimetry A very simple gravimetric method for the determination of vanadium has been worked out. In acid medium vanadium is reduced to tetravalent state which forms greenish-black precipitate with 8-hydroxyquinoline (2 % in 2 mol 1-1 CH3COOH) in the presence of ammonium acetate. The precipitate is dried and weighedas VO(C9H60 N)2. The con version factor for vanadium is 0.1437. The method is free from the interference of molybdenum(VI), chromium(III,VI), uranium(VI), selenium(IV), arsenic(I1I), bis muth(III), lead(U), calcium(II), manganese(I1) and maguesium(II). Opracowanoprosta wagow'\ metode oznaczania wanadu. Wauad(V) redukuje silt w kwasnym roztworze do wanadu(IV), ktory w obecnosci octanuamonu tworzy z 8-hydro ksychinolina (2 % roztwor w 2 mol 1-1CH3COOH) zielonoczaruy osad. Po wysuszeniu osad jestwazonyjako VO(C9H60 Nh Mnoznik analityczny wynosi dla wanadu 0,1437. W oznaczeniu nie przeszkadzaja: molibden(VI), chrom(III,VI), uran(VI), selen(IV), arsen(III), bizmut(III), o16w(II), wapriffl), mangan(II} i magnez(II), Many inorganic [1-4a] and organic [5-8, 11] precipitants employed for the estimation of vanadium in milligram amounts are. unsuitable for routine analysis, either because they are not quantitative or because other elements are coprecipitated withvanadium, and also in some cases, the precipitate formed does not have a definite composition. Cup ferron [4b] is generally recommended for the precipitation of vanadium, but several precautions are necessary because ofthe instability of cupfer ron and many other elements are precipitated by the reagent under conditions ofthe * Senior author for correspondence. -
(DAP) Diammonium Phosphate Safety Data Sheet 200 Revision Date:04/30/2015 : Version: 1.0
(DAP) Diammonium phosphate Safety Data Sheet 200 Revision date:04/30/2015 : Version: 1.0 SECTION 1: Identification of the substance/mixture and of the company/undertaking 1.1. Product identifier Product form : Substance Substance name : (DAP) Diammonium phosphate Product code : DAP, DAPFR,DAPOS, DAPLG CAS No. : 7783-28-0 Formula : (NH4)2HPO4 Synonyms : Ammonium phosphate, dibasic / Diammonium hydrogenorthophosphate / Phosphoric acid, diammonium salt / Diammonium hydrogenphosphate / Ammonium phosphate dibasic / Diammonium hydrogen phosphate / Diammonium hydrogen orthophosphate / Phosphoric acid, ammonium salt (1:2) / DIAMMONIUM PHOSPHATE / DAP Product group : Commercial product Other means of identification : DAP, DAPLG 1.2. Relevant identified uses of the substance or mixture and uses advised against Use of the substance/preparation : Agricultural chemical No additi onal infor mati on available 1.3. Details of the supplier of the safety data sheet PCS Sales (USA), Inc. 1101 Skokie Blvd. Suite 400 Northbrook, IL 60062 T 800-241-6908 / 847-849-4200 Suite 500 122 1st Avenue South Saskatoon, Saskatchewan Canada S7K7G3 T 800-667-0403 (Canada) / 800-667-3930 (USA) [email protected] - www.PotashCorp.com 1.4. Emergency telephone number Emergency number : 800-424-9300 CHEMTREC SECTION 2: Hazards identification 2.1. Classification of the substance or mixture GHS-US classification Skin Irrit. 2 H315 Eye Irrit. 2B H320 STOT SE 3 H335 Aquatic, Acute 2 H401 04/30/2015 EN (English) SDS Ref.: 200 1/10 (DAP) Diammonium phosphate Safety Data Sheet 200 Full text of H-phrases: see section 16 2.2. Label elements GHS-US labelling Hazard pictograms (GHS-US) : GHS07 Signal word (GHS-US) : Warning Hazard statements (GHS-US) : H315 - Causes skin irritation H320 - Causes eye irritation H335 - May cause respiratory irritation H401 - Toxic to aquatic life. -
Step-By-Step Guide to Better Laboratory Management Practices
Step-by-Step Guide to Better Laboratory Management Practices Prepared by The Washington State Department of Ecology Hazardous Waste and Toxics Reduction Program Publication No. 97- 431 Revised January 2003 Printed on recycled paper For additional copies of this document, contact: Department of Ecology Publications Distribution Center PO Box 47600 Olympia, WA 98504-7600 (360) 407-7472 or 1 (800) 633-7585 or contact your regional office: Department of Ecology’s Regional Offices (425) 649-7000 (509) 575-2490 (509) 329-3400 (360) 407-6300 The Department of Ecology is an equal opportunity agency and does not discriminate on the basis of race, creed, color, disability, age, religion, national origin, sex, marital status, disabled veteran’s status, Vietnam Era veteran’s status or sexual orientation. If you have special accommodation needs, or require this document in an alternate format, contact the Hazardous Waste and Toxics Reduction Program at (360)407-6700 (voice) or 711 or (800) 833-6388 (TTY). Table of Contents Introduction ....................................................................................................................................iii Section 1 Laboratory Hazardous Waste Management ...........................................................1 Designating Dangerous Waste................................................................................................1 Counting Wastes .......................................................................................................................8 Treatment by Generator...........................................................................................................12 -
SIAM 24, 17-20 April 2007 US/ICCA
SIAM 24, 17-20 April 2007 US/ICCA SIDS INITIAL ASSESSMENT PROFILE CAS Nos. 7722-76-1, 7783-28-0, 68333-79-9, 8011-76-5, 65996-95-4 Phosphate category: Monoammonium phosphate (MAP), Chemical Names Diammonium phosphate (DAP), Ammonium polyphosphate (APP), Single superphosphate (SSP), Triple superphosphate (TSP) MAP: NH4H2PO4 DAP: (NH4)2HPO4 Structural Formula APP: SSP: main components:Ca(H2PO4)2. H2O /CaSO4.H2O TSP: CaHPO4.2H2O SUMMARY CONCLUSIONS OF THE SIAR Category/Analogue Rationale The category consists of monoammonium phosphate (MAP; CAS No. 7722-76-1), diammonium phosphate (DAP; CAS No. 7783-28-0), ammonium polyphosphate (APP; CAS No. 68333-79-9), single superphosphate (SSP; CAS No. 8011-76-5), and triple superphosphate (TSP; CAS No. 65996-95-4). All members of the category are mainly or exclusively used as fertilizer and have one common functional group (phosphate) that equilibrates between several different ionic species - = = -3 [H3PO4, H2PO4 , HPO4 , HPO4 , or PO4 ] depending on the pH of the environment. Thus, chemical reactions for all compounds in this category are similar with the exception of the actual dissociation product, which forms calcium or ammonia along with common phosphate moieties. However, the presence of the ammonium ion will influence the observed toxicity and its data are used to conservatively represent the toxicity of the category members. Under typical environmental conditions, the phosphate would be present as monohydrogen = - - phosphate (HPO4 ) or dihydrogen phosphate (H2PO4 ) with the equilibrium favoring H2PO4 as the acidity of the environment increases. Under these conditions, the proportions of phosphoric acid -3 (H3PO4) and the phosphate anion (PO4 ) would be extremely low. -
Chemical Analyses for Selected Minor Elements in Pierre Shale
Chemical Analyses for Selected Minor Elements in Pierre Shale GEOLOGICAL SURVEY PROFESSIONAL PAPER 391-A Chemical Analyses for Selected Minor Elements in Pierre Shale By L. F. RADER and F. S. GRIMALDI ANALYTICAL METHODS IN GEOCHEMICAL INVESTIGATIONS OF THE PIERRE SHALE GEOLOGICAL SURVEY PROFESSIONAL PAPER 391-A UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON : 1961 UNITED STATES DEPARTMENT OF THE INTERIOR STEW ART L. UDALL, Secretary GEOLOGICAL SURVEY Thomas B. Nolan, Director For sale by the Superintendent of Documents, U.S. Government Printing Office Washington 25, D.C. CONTENTS Page Page Abstract--_________________________________________ A-l Methods for the determination of individual Introduction ___-----_-_--_________________-__--__-_ 1 constituents Continued General remarks._________________________ ______ 1 Copper lead, and zinc Continued Laboratories. -._---____-_-______________________ 2 Zinc, dithizone method._____^_______________ A-20 Acknowledgments. ___-_-_-_--______--_-_________ 2 Lead, dithizone method______------_-____-__- 22 Division of work________________________________ 2 Arsenic.___________,__________-_-_--___-__---_- 23 Methods selected and treatment of data ___________ 3 Acid digestion, heteropoly blue method________ 23 Sample preparation _________________________________ 4 Alternative fusion-heteropoly blue method_____ 24 Methods for the determination of individual constituents. 4 Titanium. _____________________________________ 4 Selenium, distillation, visual-estimation method.____ 25 Peroxide method._--_--_-____._____________ 4 Molybdenum and tungsten______-____------_---_- 27 Alternative tiron method, ___________________ 5 Isolation by method 1, alpha-benzoinoxime pre Vanadium. _--.---_____-_-___.__________________ 7 cipitation. ___----_-_-_-__--_----_-----_-- 27 Fusion-leach separation method. _____________ 7 Isolation by alternative method 2, alpha-ben Alternative cupferron separation method...... -
Prohibited and Restricted Chemical List
School Emergency Response Plan and Management Guide Prohibited and Restricted Chemical List PROHIBITED AND RESTRICTED CHEMICAL LIST Introduction After incidents of laboratory chemical contamination at several schools, DCPS, The American Association for the Advancement of Science (AAAS) and DC Fire and Emergency Management Services developed an aggressive program for chemical control to eliminate student and staff exposure to potential hazardous chemicals. Based upon this program, all principals are required to conduct a complete yearly inventory of all chemicals located at each school building to identify for the removal and disposal of any prohibited/banned chemicals. Prohibited chemicals are those that pose an inherent, immediate, and potentially life- threatening risk, injury, or impairment due to toxicity or other chemical properties to students, staff, or other occupants of the school. These chemicals are prohibited from use and/or storage at the school, and the school is prohibited from purchasing or accepting donations of such chemicals. Restricted chemicals are chemicals that are restricted by use and/or quantities. If restricted chemicals are present at the school, each storage location must be addressed in the school's written emergency plan. Also, plan maps must clearly denote the storage locations of these chemicals. Restricted chemicals—demonstration use only are a subclass in the Restricted chemicals list that are limited to instructor demonstration. Students may not participate in handling or preparation of restricted chemicals as part of a demonstration. If Restricted chemicals—demonstration use only are present at the school, each storage location must be addressed in the school's written emergency plan. Section 7: Appendices – October 2009 37 School Emergency Response Plan and Management Guide Prohibited and Restricted Chemical List Following is a table of chemicals that are Prohibited—banned, Restricted—academic curriculum use, and Restricted—demonstration use only. -
FLUID COMPATIBILITY CHART for Metal Threaded Fittings Sealed with Loctite¨ Sealants LIQUIDS, SOLUTIONS & SUSPENSIONS
FLUID COMPATIBILITY CHART for metal threaded fittings sealed with Loctite® Sealants LIQUIDS, SOLUTIONS & SUSPENSIONS LEGEND: Bagasse Fibers.......................... Chlorobenzene Dry ................... Ferrous Chloride ...................... Ion Exclusion Glycol ................. Nickel Chloride.......................... All Loctite® Anaerobic Sealants are Barium Acetate ........................ Chloroform Dry......................... Ferrous Oxalate......................... Irish Moss Slurry...................... Nickel Cyanide ......................... Compatible Including #242®, 243, Barium Carbonate..................... Chloroformate Methyl............... Ferrous Sulfate10%.................. Iron Ore Taconite ..................... Nickel Fluoborate ..................... 542, 545, 565, 567, 569, 571, 572, Barium Chloride........................ Chlorosulfonic Acid .................. Ferrous Sulfate (Sat)................. Iron Oxide ................................ Nickel Ore Fines ....................... 577, 580, 592 Barium Hydroxide..................... Chrome Acid Cleaning .............. Fertilizer Sol ............................. Isobutyl Alcohol ....................... Nickel Plating Bright ................. † Use Loctite® #270, 271™, 277, 554 Barium Sulfate.......................... Chrome Liquor.......................... Flotation Concentrates.............. Isobutyraldehyde ..................... Nickel Sulfate ........................... Not Recommended Battery Acid .............................. Chrome Plating -
New Methods for the Determination of Trace Quantities of Vanadium. Sham Lal Sachdev Louisiana State University and Agricultural & Mechanical College
Louisiana State University LSU Digital Commons LSU Historical Dissertations and Theses Graduate School 1966 New Methods for the Determination of Trace Quantities of Vanadium. Sham Lal Sachdev Louisiana State University and Agricultural & Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_disstheses Recommended Citation Sachdev, Sham Lal, "New Methods for the Determination of Trace Quantities of Vanadium." (1966). LSU Historical Dissertations and Theses. 1135. https://digitalcommons.lsu.edu/gradschool_disstheses/1135 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Historical Dissertations and Theses by an authorized administrator of LSU Digital Commons. For more information, please contact [email protected]. This dissertation has been microfilmed exactly as received SACHDEV, Sham Lai, 1937- NEW METHODS FOR THE DETERMINATION OF TRACE QUANTITIES OF VANADIUM. Louisiana State University, Ph.D., 1966 Chemistry, analytical University Microfilms, Inc., Ann Arbor, Michigan NEW METHODS FOR THE DETERMINATION OF TRACE QUANTITIES OF VANADIUM A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Doctor of Philosophy in The Department of Chemistry by Sham Lai Sachdev B.S., Panjab University, 1959 M.S.., Pan jab University, i960 January, 1966 ACKNOWLEDGMENTS The author wishes to express his gratitude to Professor Philip W. West for directing this research. He also wishes to express his appreciation for the help and encouragement extended to him by Dr. J. W. Robinson, his colleagues and many members of the graduate faculty of the Chemistry Department at Louisiana State University.