Copper disulfide

Lead(ll) azide Calcium stearate, copper, zinc, brass, carbon disulfide... 

Protein-Based Adhesives. Proteia-based adhesives are aormaHy used as stmctural adhesives they are all polyamino acids that are derived from blood, fish skin, caseia [9000-71 -9] soybeans, or animal hides, bones, and connective tissue (coUagen). Setting or cross-linking methods typically used are iasolubilization by means of hydrated lime and denaturation. Denaturation methods require energy which can come from heat, pressure, or radiation, as well as chemical denaturants such as carbon disulfide [75-15-0] or thiourea [62-56-6]. Complexiag salts such as those based upon cobalt, copper, or chromium have also been used. Formaldehyde and formaldehyde donors such as h exam ethyl en etetra am in e can be used to form cross-links. Removal of water from a proteia will also often denature the material. 

AEROPHINE 3418A promoter is widely used ia North and South America, AustraHa, Europe, and Asia for the recovery of copper, lead, and ziac sulfide minerals (see Elotatton). Advantages ia comparison to other collectors (15) are said to be improved selectivity and recoveries ia the treatment of complex ores, higher recoveries of associated precious metals, and a stable grade—recovery relationship which is particularly important to the efficient operation of automated circuits. Additionally, AEROPHINE 3418A is stable and, unlike xanthates (qv), does not form hazardous decomposition products such as carbon disulfide. It is also available blended with other collectors to enhance performance characteristics. 

The reactive species that iaitiate free-radical oxidatioa are preseat ia trace amouats. Exteasive studies (11) of the autoxidatioa mechanism have clearly estabUshed that the most reactive materials are thiols and disulfides, heterocycHc nitrogen compounds, diolefins, furans, and certain aromatic-olefin compounds. Because free-radical formation is accelerated by metal ions of copper, cobalt, and even iron (12), the presence of metals further compHcates the control of oxidation. It is difficult to avoid some metals, particularly iron, ia fuel systems. 

Carbon disulfide is normally stored and handled in mild steel equipment. Tanks and pipes are usually made from steel. Valves are typically cast-steel bodies with chrome steel trim. Lead is sometimes used, particularly for pressure reUef disks. Copper and copper alloys are attacked by carbon disulfide and must be avoided. Carbon disulfide Hquid and vapor become very corrosive to iron and steel at temperatures above about 250°C. High chromium stainless steels, glass, and ceramics maybe suitable at elevated temperatures. 

Acetylene works Acrylates works Aldehyde works Aluminum works Amines works Ammonia works Anhydride works Arsenic works Asbestos works Benzene works Beryllium works Bisulfate works Bromine works Cadmium works Carbon disulfide works Carbonyl works Caustic soda works Cement works Ceramic works Chemical fertilizer works Chlorine works Chromium works Copper works Di-isocyanate works Electricity works Fiber works Fluorine works Gas liquor works Gas and coke works Hydrochloric acid works Hydrofluoric acid works Hydrogen cyanide works Incineration works Iron works and steel works... 

The name xanthate, derived from the Greek "xanthos (meaning blond), was coined by Zeiss in 1815, because the copper complexes that he isolated had a characteristic yellow color (22). Xanthates are formed by nucleophilic addition of an alkoxide ion to carbon disulfide. 

A hydroxy and an arylthio group can be added to a double bond by treatment with an aryl disulfide and lead tetraacetate in the presence of trifluoroacetic acid." Manganese and copper acetates have been used instead of Pb(OAc)4. ° Addition of the groups OH and RSO has been achieved by treatment of alkenes with O2 and a thiol (RSH)." Two RS groups were added, to give vie- dithiols, by treatment of the alkene with a disulfide RSSR and Bp3-etherate."° This reaction has been carried... 

Electrodeposition of copper indium disulfide (CulnS2) has been reported [180-182], In a typical instance, single-phase polycrystalline CuInS2 thin films composed of 1-3 fim sized crystallites were grown on Ti by sulfurization of Cu-ln precursors prepared by sequentially electrodeposited Cu and In layers [183]. In this work, solar cells were fabricated by electrodepositing ZnSe on CuInS2. Cyclic... 

The reaction of metallic copper with thiuram disulfides yields complexes of Cu I), which are polymeric in solution as well as in the solid state 121,122). In 123) the copper atoms are located at the corners of a slightly distorted tetrahedron with Cu—Cu distances ranging from 2.6—2.7 A. Each of the copper atoms is coordinated to three sulfur atoms in a nearly planar triangular arrangement and each sulfur atom coordinates one or two copper atoms. 

For the spectrophotometric method, the evolved carbon disulfide is reacted with copper acetate and diethylamine to form a yellow copper complex which can be measured at 435 nm." The recoveries range between 70 and 90%. Reproducibility of this method was improved by reducing the time and the mode of sample pretreatment. Since all alkylenebis(dithiocarbamates) decompose to carbon disulfide by acid degradation, the above analytical methods are not selective. The result is the measured total residues of all alkylenebis(dithiocarbamates) related products. However, this method is recommended as standard method S15 for alkylenebis(dithiocarbamates) by the German Research Association. ... 

Changing the carbon disulfide trapping agent from copper acetate and diethylamine solution to methanolic potassium hydroxide to produce a xanthogenate increases the method s reproducibility and sensitivity. " ... 

Dermal Effects. Skin irritation was noted in wildlife officers at the RMA after they handled sick or dead ducks without gloves (NIOSH 1981). Although the investigators concluded that diisopropyl methylphosphonate contributed to the local effects, a number of other compounds were present. Analysis of the pond water indicated the presence of a number of organic and inorganic contaminants, including diisopropyl methylphosphonate (11.3 ppm) aldrin (0.368 ppm) dieldrin (0.0744 ppm) dicyclo-pentadiene, bicycloheptadiene, diethyl benzene, dimethyl disulfide, methyl acetate, methyl isobutyl ketone, toluene, and sodium (49,500 ppm) chloride (52,000 ppm) arsenic (1,470 ppm) potassium (180 ppm) fluoride (63 ppm) copper (2.4 ppm) and chromium (0.27 ppm). Because of the presence of numerous compounds, it is unclear whether diisopropyl methylphosphonate was related to the irritation. 

During preparation of aluminium copper(I) disulfide from the elements in an air-free silica tube at 900-1000° C, initial heating must be slow to prevent explosion of the tube by internal pressure of unreacted sulfur vapour. 

Novel example of this reaction type are given by the copper-catalyzed decomposition of ethyl diazoacetate in the presence of bis(dialkoxyphosphoryl)disulfides 374 350 where P/S insertion sometimes accompanies the S/S insertion, and of bis(dialkoxy-thiophosphoryl)trisulfides 375 351 where desulfurization to give the disulfide derived product occurs during the reaction. Only P/S insertion product was obtained from bis(dialkoxyphosphoryl)trisulfide or -tetrasulfide 376 the copper-catalyst is dispensable in this case351K... 

These reactions, which were promoted either by copper (bronze or powder) or BF3 Et20, are completely analogous to those of disulfides. 

Metallothioneins (MT) are unique 7-kDa proteins containing 20 cysteine molecules bounded to seven zinc atoms, which form two clusters with bridging or terminal cysteine thiolates. A main function of MT is to serve as a source for the distribution of zinc in cells, and this function is connected with the MT redox activity, which is responsible for the regulation of binding and release of zinc. It has been shown that the release of zinc is stimulated by MT oxidation in the reaction with glutathione disulfide or other biological disulfides [334]. MT redox properties led to a suggestion that MT may possesses antioxidant activity. The mechanism of MT antioxidant activity is of a special interest in connection with the possible antioxidant effects of zinc. (Zinc can be substituted in MT by some other metals such as copper or cadmium, but Ca MT and Cu MT exhibit manly prooxidant activity.)... 

Hollingsworth, J. A. Hepp, A. F. Buhro, W. E. 1999. Spray CVD of copper indium disulfide films Control of microstructure and crystallographic orientation. Chem. Vap. Deposition 5 105-108. 

Lead(II) azide Lead chromate Lead dioxide Calcium stearate, copper, zinc, brass, carbon disulfide Iron hexacyanoferrate(4-) Aluminum carbide, hydrogen peroxide, hydrogen sulfide, hydroxylamine, ni-troalkanes, nitrogen compounds, nonmetal halides, peroxoformic acid, phosphorus, phosphorus trichloride, potassium, sulfur, sulfur dioxide, sulfides,... 

Copper is part of several essential enzymes including tyrosinase (melanin production), dopamine beta-hydroxylase (catecholamine production), copper-zinc superoxide dismutase (free radical detoxification), and cytochrome oxidase and ceruloplasmin (iron conversion) (Aaseth and Norseth 1986). All terrestrial animals contain copper as a constituent of cytochrome c oxidase, monophenol oxidase, plasma monoamine oxidase, and copper protein complexes (Schroeder et al. 1966). Excess copper causes a variety of toxic effects, including altered permeability of cellular membranes. The primary target for free cupric ions in the cellular membranes are thiol groups that reduce cupric (Cu+2) to cuprous (Cu+1) upon simultaneous oxidation to disulfides in the membrane. Cuprous ions are reoxidized to Cu+2 in the presence of molecular oxygen molecular oxygen is thereby converted to the toxic superoxide radical O2, which induces lipoperoxidation (Aaseth and Norseth 1986). 

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