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Zinc Fluoride Product Stewardship Summary February 2011
Zinc Fluoride Product Stewardship Summary February 2011 ZnF2 Chemical Name: Zinc Fluoride Chemical Category (if applicable): Metal Halide Synonyms: Zinc difluoride; ZnF2 CAS Number: 7783-49-5 CAS Name: Zinc fluoride EC (EINECS) Number: 232-001-9 Document Number: GPS0041 V1.0 Zinc fluoride (ZnF2) is used in the manufacture of metals, in fluxes, chemical synthesis, and in the manufacture of special glasses.. Exposure can occur at either a ZnF2 manufacturing facility or at other manufacturing, packaging or storage facilities that handle ZnF2. Persons involved in maintenance, sampling and testing activities, or in the loading and unloading of ZnF2 packages 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 ZnF2 is a component of consumer products, users should follow manufacturer’s use and/or label instructions. ZnF2 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. ZnF2 s a nonflammable solid that is stable under normal conditions. Contact of ZnF2 with water or extended skin contact under moist conditions can produce hydrofluoric acid (HF), a very dangerous acid. Breathing ZnF2 dust can irritate the nose, throat, and lungs. Short-term exposure to high concentrations of ZnF2 may cause nausea, vomiting, loss of appetite and weakness. Long-term exposure to ZnF2 may cause deposits of fluorides in bones and teeth, a condition called fluorosis, which may result in pain, disability and discoloration or mottling of teeth. -
Electronic Supplementary Material (ESI) for Chemcomm. This Journal Is © the Royal Society of Chemistry 2016
Electronic Supplementary Material (ESI) for ChemComm. This journal is © The Royal Society of Chemistry 2016 Colloidal Atomic Layer Deposition Growth of PbS/CdS Core/Shell Quantum Dots Michel Nasilowski,a Lea Nienhaus,a Sophie N. Bertram,a Moungi. G. Bawendia,* Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA. *e-mail: [email protected] Supplementary Information Experimental methods Chemicals: Sulfur (Aldrich, 99.998%), oleylamine (OLA, Aldrich, technical grade 70%), lead chloride (PbCl2, Alfa-Aesar, 99.999%), hexanes (Omnisolv, 98.5%), formamide (FA, Sigma-Aldrich, >99%), ammonium sulfide ((NH4)2S, Strem, 40-44% aqueous solution), cadmium acetate dihydrate (Cd(Ac)2, Sigma-Aldrich 98%), cadmium oxide (CdO, Alfa-Aesar, 99.998%), oleic acid (OA, Alfa-Aesar, technical grade 90%) and tetracholorethylene (Alfa-Aesar, 99%) were used without further purification. Cd(OA)2: 1.28 g of cadmium oxide in 20 mL of oleic acid was heated at 160°C for 1 hour under nitrogen until colorless. The solution was then degassed under vacuum at 70°C for 30 min. Synthesis of PbS QDs: The synthesis of PbS QDs was adapted from a previously reported procedure.1,2 0.080g of sulfur in 7.5 mL OLA was heated at 120°C for 20 min under nitrogen bubbling and stirring. 0.83g of PbCl2 in 15 mL OLA was degassed for 30 minutes at room temperature, then under nitrogen, the temperature was increased to 120°C (with a vacuum pull at 110°C for ~5min). Once the temperature was stable at 120°C, 2.5mL of the sulfur solution was swiftly injected into the lead solution. -
Evaluation of Antibacterial and Cytocompatible Properties Of
Dental Materials Journal 2020; : – Evaluation of antibacterial and cytocompatible properties of multiple-ion releasing zinc-fluoride glass nanoparticles Erika NISHIDA1, Hirofumi MIYAJI1, Kanako SHITOMI1, Tsutomu SUGAYA1 and Tsukasa AKASAKA2 1 Department of Periodontology and Endodontology, Faculty of Dental Medicine, Hokkaido University, N13 W 7, Kita-ku, Sapporo, Hokkaido 060- 8586, Japan 2 Department of Biomedical Materials and Engineering, Faculty of Dental Medicine, Hokkaido University, N13 W 7, Kita-ku, Sapporo, Hokkaido 060- 8586, Japan Corresponding author, Hirofumi MIYAJI; E-mail: [email protected] Zinc-fluoride glass nanoparticles (Zinc-F) release several ions, such as fluoride, zinc and calcium ions, through acid-base reactions. The aim of this study was to evaluate the antibacterial and cytotoxic properties of Zinc-F. Antibacterial tests showed that a Zinc-F eluting solution significantly reduced the turbidity and colony-forming units ofStreptococcus mutans and Actinomyces naeslundii, compared to that of calcium-fluoroaluminosilicate glass nanoparticles without zinc ions. In live/dead staining, Zinc-F eluate significantly decreased green-stained bacterial cells, indicating live cells, compared with the control (no application). Human dentin coated with Zinc-F showed suppressed S. mutans and A. naeslundii biofilm formation. Additionally, Zinc-F eluate showed low cytotoxic effects in osteoblastic and fibroblastic cells. Therefore, our findings suggested that Zinc-F exhibits antibacterial and biocompatible properties through multiple-ion release. Keywords: Actinomyces naeslundii, Biocompatibility, Dentin, Streptococcus mutans, Zinc-fluoride glass nanoparticles calcium and silicon and a phosphoric acid solution. It is INTRODUCTION assumed that Zinc-F aggregates on the dentin surface to Root caries has become a major problem in elderly close dentinal tubules and release zinc, fluoride, calcium people with exposed tooth roots caused by aging or and silicon ions through acid-base reactions, such as periodontal disease. -
ZINC SILICOFLUORIDE CAS Number
Common Name: ZINC SILICOFLUORIDE CAS Number: 16871-71-9 RTK Substance number: 2043 DOT Number: UN 2855 Date: December 2001 ------------------------------------------------------------------------- ----------------------------------------------------------------------- HAZARD SUMMARY * Zinc Silicofluoride can affect you when breathed in and * If you think you are experiencing any work-related health by passing through your skin. problems, see a doctor trained to recognize occupational * Contact can irritate the skin and eyes. Prolonged contact diseases. Take this Fact Sheet with you. can cause skin rash and ulcers, and damage to the eyes. * Breathing Zinc Silicofluoride can irritate the nose, throat WORKPLACE EXPOSURE LIMITS and lungs causing coughing, wheezing and/or shortness of The following exposure limits are for Fluoride: (measured as breath. Fluorine): * Very high exposure can cause Fluoride poisoning with stomach pain, weakness, convulsions, collapse and death. OSHA: The legal airborne permissible exposure limit * Repeated high exposure can cause deposits of Fluorides in (PEL) is 2.5 mg/m3 averaged over an 8-hour the bones and teeth, a condition called “Fluorosis.” This workshift. may cause pain, disability and mottling of the teeth. * The above health effects do NOT occur at the level of NIOSH: The recommended airborne exposure limit is Fluoride used in water for preventing cavities in teeth. 2.5 mg/m3 averaged over a 10-hour workshift. * CONSULT THE NEW JERSEY DEPARTMENT OF HEALTH AND SENIOR SERVICES HAZARDOUS ACGIH: The recommended airborne exposure limit is SUBSTANCE FACT SHEET ON FLUORINE. 2.5 mg/m3 averaged over an 8-hour workshift. IDENTIFICATION * The above exposure limits are for air levels only. When Zinc Silicofluoride is a white, sand-like powder. -
United States Patent Office Paieated Aug
2,847,458 United States Patent Office Paieated Aug. 2, 1958 2 products of the reaction. Thus it is not surprising that either no structures or incorrect structures have been 2,847,458 assigned to them. Generally these reaction products of the prior art have been reacted with other materials PREPARATION OF ARYLPHOSPHONCACDS such as organic and inorganic bases, metal sulfides, al Tsai H. 'Chao, Somerville, Hans Z. Lecher, Painfield, and cohols, phenols, thiols, aluminum chloride and other Ruth A. Greenwood, Somerville, N. J., assignors to hydrocarbons in order to produce products which were American Cyanamid Company, New York, N. Y., a to be used as additives to mineral oils to prevent cor corporation of Maine rosion or to impart extreme pressure lubricating or de No Drawing. Application March 25, 1955 tergent properties to the oils. Some of these products Serial No. 496,934 have also been proposed as flotation agents. The prior art reaction products of aromatic hydrocar 15 Claims. (Cl. 260-500) bons with phosphorus pentasulfide have never been corn pletely hydrolyzed to form phosphonic acids. Some such This invention relates to a new process of preparing crude reaction products have been blown with steam or arylphosphonic acids. It also relates to arylthionophos nitrogen to remove malodorous thiocompounds which are phine sulfides which are new compounds and are inter formed as by-products. However, the prior art empha mediates in said process. sized that after this treatment the products still contained A number of arylphosphonic acids having the formula substantial amounts of sulfur, that is to say they were ArPO(OH) in which Ar is an aryl radical have been 20 not completely hydrolyzed. -
Oiv-Ma-As313-21.Pdf
COMPENDIUM OF INTERNATIONAL ANALYSIS OF METHODS - OIV Metatartaric acid Method OIV-MA-AS313-21 Type IV method Determination of the presence of metatartaric acid (Resolution Oeno 10/2007) 1. Introduction Metatartaric acid added to the wine to avoid tartaric precipitation is traditionally proportioned by the difference between the total tartaric acid following hot hydrolysis of metatartaric acid and natural tartaric acid preceding hydrolysis. However, taking into account the precision of the determination of tartaric acid, traces of metatartaric acid are not detectable by this method, and the additive, which is not accepted in certain countries, must therefore be characterised using a more specific method. 2. Scope Wines likely to contain traces of metatartaric acid. 3. Principle In relatively acid mediums, metatartaric acid forms an insoluble precipitate with cadmium acetate; it is the only one of all the elements present in must and wine to give such a precipitate . Note: Tartaric acid is also precipitated with cadmium acetate, but only in the presence of an alcohol content greater than 25% vol. The precipitate redissolves in water, unlike the precipitate obtained with metatartaric acid. The cadmium precipitate of metatartaric acid breaks down by heating with sodium hydroxide and releases tartaric acid. The latter produces a specific orange colour with ammonium metavanadate. 4. Reagents 4.1 Cadmium acetate solution at 5 p.100 4.1.1 Dihydrated cadmium acetate at 98% 4.1.2 Pure acetic acid 4.1.3 Distilled or demineralized water OIV-MA-AS313-21 : R2007 1 COMPENDIUM OF INTERNATIONAL ANALYSIS OF METHODS - OIV Metatartaric acid 4.1.4 Cadmium acetate solution: dissolve 5 g of cadmium acetate (4.1.1) in 99 mL of water (4.1.3) add 1 mL of pure acetic acid (4.1.2) 4.2 Sodium hydroxide 1M 4.3 Sulfuric acid 1M 4.4 Solution of ammonium metavanadate 2% w/v 4.4.1 Ammonium metavanadate 4.4.2 Trihydrated sodium acetate at 99% 4.4.3 Sodium acetate solution at 27 p. -
Thiophosphation of 2-Methyl-2-Nitro-L-Propanol and the Preparation of Monothiophosphoric Acid J
Journal of Research of the National Bureau of Standards Vol. 48, No. 4, April 1952 Research Paper 2318 Thiophosphation of 2-Methyl-2-Nitro-l-Propanol and the Preparation of Monothiophosphoric Acid J. V. Karabinos, R. A. Paulson, and W. H. Smith The thiophosphation of a nitroalcohol was studied in ether and in pyridine solution. When 2-methyl-2-nitro-l-propanol was refluxed with phosphorus pentasulfide in ether, the corresponding dithiophosphate was formed. In pyridine solution, however, a pyridine salt of the secondary dithiophosphate was formed. A pyridine salt of metatrithophosphoric acid was also isolated from the latter reaction, and this salt was hydrolyzed to pyridinium monothiophosphate. Monothiophosphoric acid monohydrate itself was obtained, for the first time, by application of ion-exchange and lyophilizing techniques to its pyridine salt. 1. Introduction HPS3 + 3H20->H3PS03 + 2H2S. The reaction of phosphorus pentasulfide with The formulas for the pyridinium salts III and IV organic hydroxy compounds reportedly [1 to 4]* may be represented as follows: yields secondary dithiophosphates (I). (C5H5N)2.HPS3. (III). C5H5N.H3PS03. (IV) (RO)2P(S)SH. (I) It is possible that substance III, rather than phos An extension of this reaction to a nitroalcohol is phorus pentasulfide, acts as the thiating agent in described. When 2-methyl-2-nitro-l-propanol was pyridine solution [5]. refluxed with phosphorus pentasulfide in ethyl ether, From the mother liquors obtained by the reaction a product melting at 104° G was obtained that gave of phosphorus pentasulfide with the nitroalcohol in elemental analyses and a molecular-weight value pyridine solution, still another crystalline substance .corresponding to 0,0'-bis(2-methyl-2-nitro-propyl-) was obtained; this substance melted at 103° to 104° C dithiophosphate (II). -
Chemical Name Federal P Code CAS Registry Number Acutely
Acutely / Extremely Hazardous Waste List Federal P CAS Registry Acutely / Extremely Chemical Name Code Number Hazardous 4,7-Methano-1H-indene, 1,4,5,6,7,8,8-heptachloro-3a,4,7,7a-tetrahydro- P059 76-44-8 Acutely Hazardous 6,9-Methano-2,4,3-benzodioxathiepin, 6,7,8,9,10,10- hexachloro-1,5,5a,6,9,9a-hexahydro-, 3-oxide P050 115-29-7 Acutely Hazardous Methanimidamide, N,N-dimethyl-N'-[2-methyl-4-[[(methylamino)carbonyl]oxy]phenyl]- P197 17702-57-7 Acutely Hazardous 1-(o-Chlorophenyl)thiourea P026 5344-82-1 Acutely Hazardous 1-(o-Chlorophenyl)thiourea 5344-82-1 Extremely Hazardous 1,1,1-Trichloro-2, -bis(p-methoxyphenyl)ethane Extremely Hazardous 1,1a,2,2,3,3a,4,5,5,5a,5b,6-Dodecachlorooctahydro-1,3,4-metheno-1H-cyclobuta (cd) pentalene, Dechlorane Extremely Hazardous 1,1a,3,3a,4,5,5,5a,5b,6-Decachloro--octahydro-1,2,4-metheno-2H-cyclobuta (cd) pentalen-2- one, chlorecone Extremely Hazardous 1,1-Dimethylhydrazine 57-14-7 Extremely Hazardous 1,2,3,4,10,10-Hexachloro-6,7-epoxy-1,4,4,4a,5,6,7,8,8a-octahydro-1,4-endo-endo-5,8- dimethanonaph-thalene Extremely Hazardous 1,2,3-Propanetriol, trinitrate P081 55-63-0 Acutely Hazardous 1,2,3-Propanetriol, trinitrate 55-63-0 Extremely Hazardous 1,2,4,5,6,7,8,8-Octachloro-4,7-methano-3a,4,7,7a-tetra- hydro- indane Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]- 51-43-4 Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]-, P042 51-43-4 Acutely Hazardous 1,2-Dibromo-3-chloropropane 96-12-8 Extremely Hazardous 1,2-Propylenimine P067 75-55-8 Acutely Hazardous 1,2-Propylenimine 75-55-8 Extremely Hazardous 1,3,4,5,6,7,8,8-Octachloro-1,3,3a,4,7,7a-hexahydro-4,7-methanoisobenzofuran Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime 26419-73-8 Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime. -
United States Patent Office Patented June 25, 1963
3,095,356 United States Patent Office Patented June 25, 1963 1. 2 3,095,356 of fluoride uptake by the teeth. Soluble fluorides are DENTIFRICE COMPRISING INSOLUBLE SODIUM found to be taken up to a greater extent when these metal METAPHOSPHATE AND A CADMUM, TN, saits are also present with the fluoride. The proportion ZINC, MANGANESE OR IRON COMPOUND TO of the fluorides, such as aluminum, tin, or sodium fluoride INHIBIT CALCUM ON SEQUESTERNG employed in the practice of the present invention is in the Henry V. Moss, Clayton, Mo, assignor to Monsanto range of 0.05 to 1% by weight of the dentifrice composi Chemical Company, St. Louis, Mo., a corporation of tion. However, the total proportion of metal compounds Delaware w of the group of cadmium, tin, zinc, manganese, alumi No Drawing. Filed Feb. 20, 1956, Ser. No. 566,353 num and iron which are present in the dentifrice is within 11 Claims. (CI. 167-93) 10 the broader range of 0.05 to 50 weight percent. This invention relates to polishing compositions suitable According to one of the present theories as to the for use as a dentifrice base and particularly to those com molecular aggregation of phosphate salts, the insoluble positions which contain the insoluble form of sodium sodium metaphosphate containing the usual impurities, metaphosphate as an ingredient thereof. may exist as a chain-type of molecular structure, and also An object of the present invention is the provision of 5 in the form of relatively short-chain polyphosphates. Ac an improved identifice. - cording to this theory, the presently employed metal com The use of the so-called insoluble form of sodium pounds control the sequestering action of polyphosphates, metaphosphate in finely divided form has been proposed thereby controlling the type of molecular structures pre as a dentifrice. -
638 Subpart A—Phosphorus Production Subcategory Subpart B
§ 422.10 40 CFR Ch. I (7–1–12 Edition) Subpart A—Phosphorus Subpart D—Defluorinated Production Subcategory Phosphate Rock Subcategory § 422.10 Applicability; description of SOURCE: 41 FR 25975, June 23, 1976, unless the phosphorus production sub- otherwise noted. category. The provisions of this subpart are ap- § 422.40 Applicability; description of plicable to discharges of pollutants re- the defluorinated phosphate rock sulting from the production of phos- subcategory. phorus and ferrophosphorus by smelt- The provisions of this subpart are ap- ing of phosphate ore. plicable to discharges resulting from the defluorination of phosphate rock Subpart B—Phosphorus by application of high temperature treatment along with wet process phos- Consuming Subcategory phoric acid, silica and other reagents. § 422.20 Applicability; description of the phosphorus consuming sub- § 422.41 Specialized definitions. category. For the purpose of this subpart: The provisions of this subpart are ap- (a) Except as provided below, the gen- plicable to discharges of pollutants re- eral definitions, abbreviations, and sulting from the manufacture of phos- methods of analysis set forth in 40 CFR phoric acid, phosphorus pentoxide, part 401 shall apply to this subpart. (b) The term phosphorus pentasulfide, phosphorus process waste water means any water which, during manu- trichloride, and phosphorus facturing or processing, comes into di- oxychloride directly from elemental rect contact with or results from the phosphorus. The production of phos- production or use of any raw material, phorus trichloride and phosphorus intermediate product, finished product, oxychloride creates waste water pollut- by-product, or waste product. The term ants not completely amenable to the ‘‘process waste water’’ does not include procedures utilized for best practicable contaminated nonprocess waste water, control technology currently available. -
Qt4gj5w6d6 Nosplash 07E474c
This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. Article Cite This: ACS Omega 2019, 4, 5486−5495 http://pubs.acs.org/journal/acsodf Mechanochemical Synthesis, Accelerated Aging, and Thermodynamic Stability of the Organic Mineral Paceite and Its Cadmium Analogue ‡ † ‡ † § ‡ § Shaodi Li, , Igor Huskic,́, Novendra Novendra, Hatem M. Titi, Alexandra Navrotsky,*, ‡ and Tomislav Frisčič*́, ‡ Department of Chemistry, McGill University, 801 Sherbrooke St. W., H3A 0B8 Montreal, Canada § Peter A. Rock Thermochemistry Laboratory and NEAT ORU, University of California Davis, One Shields Avenue, Davis, California 95616, United States *S Supporting Information ABSTRACT: We demonstrate the use of ball milling mechanochemistry for rapid, simple, and materials-efficient · synthesis of the organic mineral paceite CaCu(OAc)4 6H2O (where OAc− is the acetate ion), composed of coordination polymer chains containing alternating Ca2+ and Cu2+ ions, as · well as its cadmium-based analogue CaCd(OAc)4 6H2O. While the synthesis of paceite in aqueous solutions requires a high excess of the copper precursor, mechanochemistry permits the use of stoichiometric amounts of reagents, as well as the use of poorly soluble and readily accessible calcium carbonate or hydroxide reactants. As established by thermochemical measurements, enthalpies of formation of both synthetic paceite and its cadmium analogue relevant to the mechanochemical reactions are highly exothermic. Reactions can also be conducted using accelerated aging, a synthetic technique that mimics geological processes of mineral weathering. Accelerated aging reactivity involving copper(II) acetate monohydrate (hoganite) and calcium carbonate (calcite) provides a potential explanation of how complex organic minerals like paceite could form in a geological environment. -
Synthesis and Characterization of Surface-Capped, Size-Quantized Cds Clusters
1322 J. Am. Chem. SOC.1990, I12, 1322-1 326 Synthesis and Characterization of Surface-Capped, Size-Quantized CdS Clusters. Chemical Control of Cluster Size Norman Henon,**+Ying Wang,+ and Hellmut Eckert* Contribution No. 4743 from E.I. du Pont de Nemouts & Company, Central Research and Development Department, P.O.Box 80328, Wilmington, Delaware 19880-0328, and Department of Chemistry, University of California at Santa Barbara, Santa Barbara, California 93106. Received May 8, I989 Abstract: Clusters of CdS in the quantum confinement regime C5O-A diameter are prepared in a rational technique whereby the cluster size and its distribution are controlled by chemical means. Competitive reaction chemistry between CdS core cluster growth and surface capping by thiophenolateleads to clusters whose core is essentially sphalerite CdS but whose reactive surface has been passivated by covalently attached phenyl groups. Adjustment of the sulfide to thiophenol ratio during synthesis takes advantage of the competitive reaction rates of these species with Cd ions to control the eventual cluster size. The clusters remain soluble in several organic solvents but may be isolated as stable powders and subsequently redissolved. The Cd "'NMR data for this series of capped clusters confirm the presence of sphalerite CdS as the cluster core and the increasing percentage of Cd involved in this core as the S/SPh ratio increases. Optical properties demonstrate well-behaved absorption edge and emission band shifts with development of exciton features as the clusters grow. Colloidal semiconductor species are currently under intense combustion (C + H) and atomic absorption were performed by Galbraith investigation as examples of nonmolecular materials that dem- Co., Knoxville, TN.