Appendix a Disposal Procedures by Chemical Updated 5/11/2020 Use
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. -
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 -
Chromatographic Separation of Alkaline Earth Metals Using Alpha-Hydroxyisobutyric Acid
AN ABSTRACT OF THE THESIS OF JOHN ARTHUR HAUSCHILD for the MASTER OF SCIENCE (Name) (Degree) in CHEMISTRY (ANALYTICAL) presented on (Major) Title: CHROMATOGRAPHIC SEPARATION OF ALKALINE EARTH METALS USING ALPHA-HYDROXYISOBUYRIC ACID Abstract approved: Redacted for Privacy Max B. Williams A systematic study of the elution of magnesium and calcium from Dowex 50 X 8 resin using a-hydroxyisobutyric acid (a-HIBA) at various pH values and concentrations, indicated that the difference in the equilibrium distribution coefficients of these two elements was large enough for a good separation.This fact was applied to develop a chromatographic procedure for the separationof milligram quantities of magnesium, calcium, strontium, and barium.After magnesium was eluted with 0. 22M a-HIBA at pH 4. 5, thethree remaining elements were eluted by varying the concentration and pH of a-HIBAduring the course of the elution (exponential gradient elution).After its respec- tive elution, each alkaline earth metal was directly determined by atomic absorption spectroscopy.Using this method, several success- ful analyses of synthetic samples (similar to the composition of sea water) were performed.Yield determinations of the alkaline earth metals from these analyses were consistently greater than 93%, with the overall average yield being 98%. Chromatographic Separation of Alkaline Earth Metals Using Alpha-Hydroxyisobutyric Acid by John Arthur Haus child A THESIS submitted to Oregon State University in partial fulfillment of the requirements for the degree of Master -
NON-HAZARDOUS CHEMICALS May Be Disposed of Via Sanitary Sewer Or Solid Waste
NON-HAZARDOUS CHEMICALS May Be Disposed Of Via Sanitary Sewer or Solid Waste (+)-A-TOCOPHEROL ACID SUCCINATE (+,-)-VERAPAMIL, HYDROCHLORIDE 1-AMINOANTHRAQUINONE 1-AMINO-1-CYCLOHEXANECARBOXYLIC ACID 1-BROMOOCTADECANE 1-CARBOXYNAPHTHALENE 1-DECENE 1-HYDROXYANTHRAQUINONE 1-METHYL-4-PHENYL-1,2,5,6-TETRAHYDROPYRIDINE HYDROCHLORIDE 1-NONENE 1-TETRADECENE 1-THIO-B-D-GLUCOSE 1-TRIDECENE 1-UNDECENE 2-ACETAMIDO-1-AZIDO-1,2-DIDEOXY-B-D-GLYCOPYRANOSE 2-ACETAMIDOACRYLIC ACID 2-AMINO-4-CHLOROBENZOTHIAZOLE 2-AMINO-2-(HYDROXY METHYL)-1,3-PROPONEDIOL 2-AMINOBENZOTHIAZOLE 2-AMINOIMIDAZOLE 2-AMINO-5-METHYLBENZENESULFONIC ACID 2-AMINOPURINE 2-ANILINOETHANOL 2-BUTENE-1,4-DIOL 2-CHLOROBENZYLALCOHOL 2-DEOXYCYTIDINE 5-MONOPHOSPHATE 2-DEOXY-D-GLUCOSE 2-DEOXY-D-RIBOSE 2'-DEOXYURIDINE 2'-DEOXYURIDINE 5'-MONOPHOSPHATE 2-HYDROETHYL ACETATE 2-HYDROXY-4-(METHYLTHIO)BUTYRIC ACID 2-METHYLFLUORENE 2-METHYL-2-THIOPSEUDOUREA SULFATE 2-MORPHOLINOETHANESULFONIC ACID 2-NAPHTHOIC ACID 2-OXYGLUTARIC ACID 2-PHENYLPROPIONIC ACID 2-PYRIDINEALDOXIME METHIODIDE 2-STEP CHEMISTRY STEP 1 PART D 2-STEP CHEMISTRY STEP 2 PART A 2-THIOLHISTIDINE 2-THIOPHENECARBOXYLIC ACID 2-THIOPHENECARBOXYLIC HYDRAZIDE 3-ACETYLINDOLE 3-AMINO-1,2,4-TRIAZINE 3-AMINO-L-TYROSINE DIHYDROCHLORIDE MONOHYDRATE 3-CARBETHOXY-2-PIPERIDONE 3-CHLOROCYCLOBUTANONE SOLUTION 3-CHLORO-2-NITROBENZOIC ACID 3-(DIETHYLAMINO)-7-[[P-(DIMETHYLAMINO)PHENYL]AZO]-5-PHENAZINIUM CHLORIDE 3-HYDROXYTROSINE 1 9/26/2005 NON-HAZARDOUS CHEMICALS May Be Disposed Of Via Sanitary Sewer or Solid Waste 3-HYDROXYTYRAMINE HYDROCHLORIDE 3-METHYL-1-PHENYL-2-PYRAZOLIN-5-ONE -
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. -
Pp-03-25-New Dots.Qxd 10/23/02 2:38 PM Page 379
pp-03-25-new dots.qxd 10/23/02 2:38 PM Page 379 HYDROGEN SULFIDE 379 HYDROGEN SULFIDE [7783-06-4] Formula: H2S; MW 34.08 Synonyms: sulfur hydride; sulfureted hydrogen Occurrence and Uses Hydrogen sulfide occurs in natural gas. It also is found in many sewer gases. It is a by-product of many industrial processes. Trace amounts of dis- solved H2S are found in wastewaters in equilibrium with dissolved sulfides and hydrosulfides. It also is found in volcanic eruptions, hot springs and in troposphere. The average concentration of H2S in the air is about 0.05 ppb. The most important applications of hydrogen sulfide involve the production of sodium sulfide and other inorganic sulfides. Hydrogen sulfide obtained as a by-product often is converted into sulfuric acid. It also is used in organic syn- thesis to make thiols or mercaptans. Other applications are in metallurgy for extracting nickel, copper, and cobalt as sulfides from their minerals; and in classical qualitative analytical methods for precipitation of many metals (see Reactions). It also is used in producing heavy water for nuclear reactors. Physical Properties Colorless gas; characteristic odor of rotten eggs; odor threshold 1ppm; sweetish taste; fumes in air; flammable gas, burns with a pale blue flame; refractive index at 589.3nm, 1.000644 at 0°C and 1 atm; density 1.539 g/L at 0°C; critical temperature 100.4°C; critical pressure 88.9 atm; liquefies at –60.7°C; solidifies at –85.5°C; velocity of sound 289 m/sec in H2S gas; slightly soluble in water (0.4% at 20°C); pH of a saturated aqueous solution 4.5; slight- ly acidic; diffusivity in water at 16°C, 1.77x105 cm2/sec; soluble in carbon disulfide, methanol, acetone; very soluble in N-methylpyrrolidinone and alka- nolamines (salt formation occurs: salt dissociates on heating); liquid H2S dis- solves sulfur and SO2. -
Hydrothermal Synthesis of Molybdenum Based Oxides for The
Hydrothermal synthesis of molybdenum based oxides for the application in catalysis Zur Erlangung des akademischen Grades eines DOKTORS DER NATURWISSENSCHAFTEN (Dr. rer. nat.) Fakultät für Chemie und Biowissenschaften Karlsruher Institut für Technologie (KIT) - Universitätsbereich genehmigte DISSERTATION von Dipl.-Ing. (FH) Kirsten Schuh aus Mainz Dekan: Prof. Dr. Peter Roesky Referent: Prof. Dr. Jan-Dierk Grunwaldt Korreferent: Prof. Dr. Anker Degn Jensen Tag der mündlichen Prüfung: 17. April 2014 Acknowledgements Acknowledgements I owe many thanks to a lot of people who have helped, supported and encouraged me during my doctoral studies, not just scientifically but also personally. First I would like to thank my supervisor Prof. Dr. Jan-Dierk Grunwaldt for the opportunity to complete my doctoral studies in his group and for providing me with a very interesting and diversified topic. I am grateful for the scientific freedom he gave me, the possibility to spend several months at the Technical University of Denmark as well as University of Zurich and for the opportunity to attend international conferences. I am grateful to Dr. Wolfgang Kleist for his scientific help especially with presentations and publications making the manuscripts reader friendly. I would also like to thank Prof. Dr. Anker Degn Jensen for agreeing to be my co- supervisor, for very helpful corrections and suggestions of abstracts, manuscripts and presentations and for giving me the opportunity to spend four months in his group at the Technical University of Denmark (DTU), where I felt very welcome. I am especially grateful for the help of Dr. Martin Høj, who put the selective oxidation set- up at DTU into operation, tested several of my samples for selective oxidation of propylene and performed TEM measurements of my FSP samples. -
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. -
Fine Biocompatible Powders Synthesized from Calcium Lactate and Ammonium Sulfate
ceramics Article Fine Biocompatible Powders Synthesized from Calcium Lactate and Ammonium Sulfate Maksim Kaimonov 1,* , Tatiana Shatalova 1,2 , Yaroslav Filippov 1,3 and Tatiana Safronova 1,2 1 Department of Materials Science, Lomonosov Moscow State University, Building, 73, Leninskie Gory, 1, 119991 Moscow, Russia; [email protected] (T.S.); fi[email protected] (Y.F.); [email protected] (T.S.) 2 Department of Chemistry, Lomonosov Moscow State University, Building, 3, Leninskie Gory, 1, 119991 Moscow, Russia 3 Research Institute of Mechanics, Lomonosov Moscow State University, Michurinsky pr., 1, 119192 Moscow, Russia * Correspondence: [email protected]; Tel.: +7-952-889-11-43 Abstract: Fine biocompatible powders with different phase compositions were obtained from a 0.5 M solution of ammonium sulfate (NH4)2SO4 and calcium lactate Ca(C3H5O3)2. The powder ◦ after synthesis and drying at 40 C included calcium sulfate dehydrate CaSO4·2H2O and calcite ◦ CaCO3. The powder after heat treatment at 350 C included β-hemihydrate calcium sulfate β- CaSO4·0.5H2O, γ-anhydrite calcium sulfate γ-CaSO4 and calcite CaCO3. The phase composition of ◦ powder heat-treated at 600 C was presented as β-anhydrate calcium sulfate β-CaSO4 and calcite ◦ CaCO3. Increasing the temperature up to 800 C leads to the sintering of a calcium sulfate powder β β consisting of -anhydrite calcium sulfate -CaSO4 main phase and a tiny amount of calcium oxide CaO. The obtained fine biocompatible powders of calcium sulfate both after synthesis and after heat Citation: Kaimonov, M.; Shatalova, treatment at temperature not above 600 ◦C can be recommended as a filler for producing unique T.; Filippov, Y.; Safronova, T. -
Ammonium Formate As Green Hydrogen Source for Clean Semi-Continuous Enzymatic Dynamic Kinetic Resolution of (+/-)-Ααα-Methylbenzylamine
RSC Advances Ammonium Formate as Green Hydrogen Source for Clean Semi-Continuous Enzymatic Dynamic Kinetic Resolution of (+/-)-ααα-Methylbenzylamine Journal: RSC Advances Manuscript ID: RA-ART-01-2014-000462.R1 Article Type: Paper Date Submitted by the Author: 21-Feb-2014 Complete List of Authors: Miranda, Leandro S. M.; Federal University of Rio de Janeiro, Biocatalysis and Organic Synthesis Lab, Chemistry Institute de Souza, Rodrigo Octavio; Federal University of Rio de Janeiro, de Miranda, Amanda; Federal University of Rio de Janeiro, Page 1 of 21 RSC Advances Graphical Abstract RSC Advances Page 2 of 21 Ammonium Formate as Green Hydrogen Source for Clean Semi-Continuous Enzymatic Dynamic Kinetic Resolution of (+/-)-α- Methylbenzylamine Amanda S. de Miranda, [a] Rodrigo O. M. A. de Souza, [ a] Leandro S. M. Miranda [a]* Keywords: Dynamic kinetic resolution • racemic amines • continuous flow . ammonium formate. Abstract: Abstract: The chemoenzymatic dynamic kinetic resolution of (+/-)-α- Methylbenzylamine under continuous flow conditions in the presence of Pd/BaSO 4 as racemization catalyst and ammonium formate as reductant is described. Under the conditions developed good conversions and excellent enantiomeric excess are reported Page 3 of 21 RSC Advances Introduction Recently, continuous processing and biocatalysis have been elected as key green engineering research areas for sustainable manufacturing 1a and it is clear that joint efforts between these areas can lead to great improvements on continuous manufacturing in agreement with green chemistry principles 1b,c . Optically pure amines are ubiquitously present in nature and active pharmaceutical ingredients (APIs). However, their synthesis still represents an ongoing synthetic challenge that can be inferred by the great amount of work and methodologies dealing with this issue in the literature. -
Mechanochemical Catalytic Transfer Hydrogenation of Aromatic Nitro Derivatives
Article Mechanochemical Catalytic Transfer Hydrogenation of Aromatic Nitro Derivatives Tomislav Portada, Davor Margetić and Vjekoslav Štrukil * Division of Organic Chemistry and Biochemistry, Ruđer Bošković Institute, Bijenička cesta 54, 10000 Zagreb, Croatia; [email protected] (T.P.); [email protected] (D.M.) * Correspondence: [email protected]; Tel.: +385‐1‐468‐0197 Received: 15 November 2018; Accepted: 29 November 2018; Published: date Abstract: Mechanochemical ball milling catalytic transfer hydrogenation (CTH) of aromatic nitro compounds using readily available and cheap ammonium formate as the hydrogen source is demonstrated as a simple, facile and clean approach for the synthesis of substituted anilines and selected pharmaceutically relevant compounds. The scope of mechanochemical CTH is broad, as the reduction conditions tolerate various functionalities, for example nitro, amino, hydroxy, carbonyl, amide, urea, amino acid and heterocyclic. The presented methodology was also successfully integrated with other types of chemical reactions previously carried out mechanochemically, such as amide bond formation by coupling amines with acyl chlorides or anhydrides and click‐type coupling reactions between amines and iso(thio)cyanates. In this way, we showed that active pharmaceutical ingredients Procainamide and Paracetamol could be synthesized from the respective nitro‐precursors on milligram and gram scale in excellent isolated yields. Keywords: mechanochemistry; catalytic transfer hydrogenation; aromatic nitro derivatives; ammonium formate; aging; ball milling; synthesis 1. Introduction Catalytic hydrogenation is one of the most significant functional group transformation reactions in organic synthesis and numerous procedures and reagents have been developed for that purpose [1,2]. As such, the hydrogenation reaction plays one of the key roles in many industrially important processes, for example hydrogenation of carbon monoxide to methanol or in food industry for the conversion of unsaturated vegetable oils into saturated triglycerides [3]. -
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.