Chromium aluminum oxid copper oxide

Copper(II) sulfate Cumene hydroperoxide Cyanides Cyclohexanol Cyclohexanone Decaborane-14 Diazomethane 1,1-Dichloroethylene Dimethylformamide Hydroxylamine, magnesium Acids (inorganic or organic) Acids, water or steam, fluorine, magnesium, nitric acid and nitrates, nitrites Oxidants Hydrogen peroxide, nitric acid Dimethyl sulfoxide, ethers, halocarbons Alkali metals, calcium sulfate Air, chlorotrifluoroethylene, ozone, perchloryl fluoride Halocarbons, inorganic and organic nitrates, bromine, chromium(VI) oxide, aluminum trimethyl, phosphorus trioxide... 

Refractory bricks composed of oxides of magnesium, chromium, aluminum and iron and trace amounts of silica and calcium oxide are used in roofs of open hearths, sidewalls of electric furnaces and vacuum apparatus and copper converters. Such refractories are made in an arc furnace by fusing mixtures of magnesite and chrome ore. 

ELECTRON SPIN RESONANCE SPECTROSCOPY Electron spin resonance (ESR) is a technique that can also be used on aqueous samples and has been used to study the adsorption of copper, manganese, and chromium on aluminum oxides and hydroxides. Copper(II) was found to adsorb specifically on amorphous alumina and microcrystalline gibbsite forming at least one Cu-O-Al bond (McBride, 1982 McBride et al., 1984). Manganese(II) adsorbed on amorphous aluminum hydroxide was present as a hydrated outer-sphere surface complex (Micera et al., 1986). Electron spin resonance combined with electron spin-echo experiments revealed that chromium(III) was adsorbed as an outer-sphere surface complex on hydrous alumina that gradually converted to an inner-sphere surface complex over 14 days of reaction time (Karthein et al., 1991). 

The search is on for catalysts to replace those containing toxic heavy metals. The addition of hydrogen chloride to acetylene to form vinyl chloride is catalyzed by mercuric chloride. Rhodium (III) chloride on activated carbon works just as well and is much less toxic 97 It should be tried also in other addition reactions of acetylene as well as in trans-esteriflcation reactions of vinyl acetate. The reduction of 2 ethyl-2-hexenal to 2-ethylhexanol can be catalyzed by a mixture of copper, zinc, manganese, and aluminum oxides in 100% yield.98 This is said to be a replacement for carcinogenic copper chromite. In Reaction 4.15, the amount of toxic chromium(II) chloride has been reduced from stoichiometric to catalytic (9-15 mol% chromium(II) chloride) by the addition of manganese metal.99... 

CHROMIUM SODIUM OXIDE (Cr3Na207 10588-01-9) A strong oxidizer. Reacts violently with reducing agents, acids, acetic anhydride, hydrazine, combustible materials, organic substances, metal powders. Reacts with acrolein, antimony trisulfide, antimony tritelluride, arsenic pentasulfide, 1,1-dichloro-l-nitroethane, 1,3-dichloropropene, diethyl-amine, fluorine, hydrazine, potassium iodide, sodium tetraborate, sodium tetraborate decahydrate, sodium borohydride, zirconium dusts, i-trioxane. Incompatible with m-bis(trichlormethyl)benzene, hydroxylamine. Aqueous solution is caustic incompatible with acids, alcohols, aldehydes, alkylene oxides, cresols, caprolactam solution, epichlorohydrin, organic anhydrides, glycols, maleic anhydride, phenols. Attacks aluminum copper, brass, bronze, tin, zinc, especially in the presence of moisture. 

Hydrogenation is generally carried out at tanperatures of 250-280°C and pressures of 20-25 MPa. Catalysts include zinc oxide in conjunction with aluminum oxide, chromium oxide, or iron oxide, and possibly, other promoters copper chromite whose activity has been reduced by the addition of cadmium compounds and cadmium oxide on an alumina carrier. Selective hydrogenation can also be carried out in a homogenous phase with metallic soaps as catalysts. 

Non-ferrous metals may form a protective oxide layer, providing a barrier against further deterioration. The coating of aluminum, magnesium, copper, chromium, cadmimn and tin may be required, nevertheless, to protect the surface from deterioration other than oxidation, or a clear coat may be used to preserve the appearance of the virgin metal from oxidation. Zinc surfaces may require a chemical pre-treatment prior to the application of the primer and top coat, depending on the condition of the surface and type of primer used. Lead and lead alloy surfaces are easily coated with a linseed oil based primer and a compatible top coat. 

Some metals used as metallic coatings are considered nontoxic, such as aluminum, magnesium, iron, tin, indium, molybdenum, tungsten, titanium, tantalum, niobium, bismuth, and the precious metals such as gold, platinum, rhodium, and palladium. However, some of the most important poUutants are metallic contaminants of these metals. Metals that can be bioconcentrated to harmful levels, especially in predators at the top of the food chain, such as mercury, cadmium, and lead are especially problematic. Other metals such as silver, copper, nickel, zinc, and chromium in the hexavalent oxidation state are highly toxic to aquatic Hfe (37,57—60). 

The transport of pre-boiler corrosion debris to the boiler section includes the oxides of iron, copper, nickel, zinc, and chromium and results from the corrosion of pre-heaters and condensers, and the like. Specifically, equipment components variously fabricated from admiralty brass, aluminum brass, cupronickels, and stainless steels are most affected. 

As mentioned above, approximately 7% of the total sulfur present in lead ore is emitted as S02. The remainder is captured by the blast furnace slag. The blast furnace slag is composed primarily of iron and silicon oxides, as well as aluminum and calcium oxides. Other metals may also be present in smaller amounts, including antimony, arsenic, beryllium, cadmium, chromium, cobalt, copper, lead, manganese, mercury, molybdenum, silver, and zinc. This blast furnace slag is either recycled back into the process or disposed of in piles on site. About 50 to 60% of the recovery furnace output is slag and residual lead, which are both returned to the blast furnace. The remainder of this dross furnace output is sold to copper smelters for recovery of the copper and other precious metals. 

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