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Copper chromite Chromium oxide

Operation. The preheated gas stream is passed through a catalyst bed, where the catalyst initiates and promotes the oxidation of the organic without being permanently altered. The catalyst is normally an active material, such as platiniun, copper chromite, chromium, or nickel, on an inert substrate, such as honeycomb-shaped ceramic. For the catalyst to be effective, the active sites upon which the organic gas molecules react must be accessible. The buildup of polymerized material or reaction with certain metal particulates will prevent contact between active sites and the gas. A catalyst can be reactivated by removing such a coating. [Pg.665]

For example transition metal such as M0O3 and Cr203, are good catalysts for polymerization of olefins a mixture of copper on chromium oxides, called copper chromite, is used for hydrogenation and, a mixture of iron and molybdenum oxide, called iron molybdate, is used for formaldehyde formation from methanol. [Pg.41]

However, compounds known to be double oxides in the solid state are named as such for example, Cr2Cu04 (actually Cr203 CuO) is chromium(III) copper(II) oxide (and not copper chromite). [Pg.219]

Copper—cadmium and zinc—chromium oxides seem to provide most selectivity (38—42). Copper chromite catalysts are not selective. Reduction of red oil-grade oleic acid has been accompHshed in 60—70% yield and with high selectivity with Cr—Zn—Cd, Cr—Zn—Cd—Al, or Zn—Cd—A1 oxides (43). The reduction may be a homogeneously catalyzed reaction as the result of the formation of copper or cadmium soaps (44). [Pg.85]

The relatively high cost and lack of domestic supply of noble metals has spurred considerable efforts toward the development of nonnoble metal catalysts for automobile exhaust control. A very large number of base metal oxides and mixtures of oxides have been considered, especially the transition metals, such as copper, chromium, nickel, manganese, cobalt vanadium, and iron. Particularly prominent are the copper chromites, which are mixtures of the oxides of copper and chromium, with various promoters added. These materials are active in the oxidation of CO and hydrocarbons, as well as in the reduction of NO in the presence of CO (55-59). Rare earth oxides, such as lanthanum cobaltate and lanthanum lead manganite with Perovskite structure, have been investigated for CO oxidation, but have not been tested and shown to be sufficiently active under realistic and demanding conditions (60-63). Hopcalities are out-... [Pg.79]

Schlatter et al. found that their data with copper chromite agrees better with 0.7 order for CO concentrations (53). For crystals of nickel oxide and chromium oxide, Yu Yao and Kummer have found that the kinetics depend on CO or hydrocarbon around 0.55 order and depend on oxygen around 0.45 order (79). Hertl and Farrauto found evidence that CO adsorbs on copper as a carbonyl group, and adsorbs on chromium oxide as a unidentate carbonate. They found that the kinetics depends on CO to the first order, and depends on oxygen to the zero order (80). [Pg.86]

Chromium compounds as catalysts, 188 Chromium oxide in catalytic converter, 62 Chromium oxide catalysts, 175-184 formation of active component, 176,177 of Cr-C bonds, 177, 178 propagation centers formation of, 175-178 number of, 197, 198 change in, 183, 184 reduction of active component, 177 Clear Air Act of 1970, 59, 62 Cobalt oxide in catalytic converter, 62 Cocatalysts, 138-141, 152-154 Competitive reactions, 37-43 Copper chromite, oxidation of CO over, 86-88... [Pg.416]

Cuprous oxide is also reduced violently by electropositive metals as discovered in an accident which occurred with aluminium. With chromium (III) oxide the reaction enables one to make copper chromite, which is a very common catalyst. The activity of copper chromite is such that it frequently combusts at the end of the reaction. [Pg.208]

Hydrogenolyses of carboxylic acids and esters to the corresponding aldehydes seems very attractive due to their simplicity. Copper chromites are the most widely used catalysts.15 Raney copper and zinc oxide-chromium oxide have also been used for this process.16-18 The hydrogenolysis of methyl benzoate to benzaldehyde was studied on various metal oxides at 300-350°C. ZnO, Zr02 and Ce02 presented high activities and selectivities (Scheme 4.8). [Pg.124]

Catalysts suitable specifically for reduction of carbon-oxygen bonds are based on oxides of copper, zinc and chromium Adkins catalysts). The so-called copper chromite (which is not necessarily a stoichiometric compound) is prepared by thermal decomposition of ammonium chromate and copper nitrate [50]. Its activity and stability is improved if barium nitrate is added before the thermal decomposition [57]. Similarly prepared zinc chromite is suitable for reductions of unsaturated acids and esters to unsaturated alcohols [52]. These catalysts are used specifically for reduction of carbonyl- and carboxyl-containing compounds to alcohols. Aldehydes and ketones are reduced at 150-200° and 100-150 atm, whereas esters and acids require temperatures up to 300° and pressures up to 350 atm. Because such conditions require special equipment and because all reductions achievable with copper chromite catalysts can be accomplished by hydrides and complex hydrides the use of Adkins catalyst in the laboratory is very limited. [Pg.9]

COPPER-CHROMIUM OXIDE CATALYST ( COPPER CHROMITE CATALYST)... [Pg.427]

Fatty alcohols are obtained by direct hydrogenation of fatty acids or by hydrogenation of fatty acid esters. Typically, this is performed over copper catalysts at elevated temperature (170°C-270°C) and pressure (40-300 bar hydrogen) [26], By this route, completely saturated fatty alcohols are produced. In the past, unsaturated fatty alcohols were produced via hydrolysis of whale oil (a natural wax occurring in whale blubber) or by reduction of waxes with sodium (Bouveault-Blanc reduction). Today, they can be obtained by selective hydrogenation at even higher temperatures (250°C-280°C), but lower pressure up to 25 bar over metal oxides (zinc oxide, chromium oxide, iron oxide, or cadmium oxide) or partially deactivated copper chromite catalysts [26],... [Pg.96]

Copper chromite is the reaction product of copper oxide and chromium oxide. It is an important catalyst for the burning of rocket propellants ... [Pg.116]

Copper chromite, CuCr204, and mixtures of cupric oxide with chromium sesquioxide and special additives (the Adkins catalyst), dehydrogenate primary alcohols to aldehydes [354, 355] and secondary alcohols to ketones [354, 355, 356]. [Pg.15]

The copper-chromium oxide ("copper chromite") catalyst, which was developed by Adkins, has been considered to be a complement of Raney nickel for hydrogenation reactions.26 This catalyst, which is, essentially, copper supported on chromium oxide or copper-chromium oxide,22-29 is useful for the hydrogenation of esters and amides but does not affect the saturation of... [Pg.216]

Another common catalyst prepared by coprecipitation is copper-chromium oxide, also known as "copper chromite" or Adkins catalyst.23 This catalyst is prepared by the addition of copper nitrate to a solution of ammonium dichromate in ammonia giving a precipitate copper ammonium dichromate. This precipitate is filtered, dried and then calcined at 650°-800°C, or more commonly, heated with a flame to induce a thermal reaction (Eqn. 13.5). The resulting fine powder is washed with acetic acid and dried to give the copper chromite catalyst.23 A more active catalyst is prepared by adding 10% barium nitrate by weight of copper before precipitation.24,25 Copper chromite catalysts containing calcium and were found to be less effective than those having a barium promoter.25... [Pg.272]

Copper chromite and copper-chromium oxide are effective catalysts for the decarboxylation of acids in quinoline solution. An example is the decarboxylation of cis-a-phenylcinnamic acid in refluxing quinoline to c/r-stilbene the two catalysts cited... [Pg.81]

Hydrogenation Copper chromite (Lazier catalyst). Copper chromium oxide (Adkins catalyst). Lindlar catalyst (see also Lithium ethoxyacetylide, Malealdehyde, Nickel boride). Nickel catalysts. Palladium catalysts. Palladium hydroxide on carbon. Perchloric acid (promoter). Platinum catalysts. Raney catalysts, Rhenium catalysts. Rhodium catalysts. Stannous chloride. Tributylborane. Trifluoroicetic acid, Tris (triphenylphosphine)chlororhodium. [Pg.658]

Copper chromite (Lazier catalyst), 156, 975 Copper-Chromium oxide, 157 Copper powder, 157-158 Copper powder-Benzoic acid, 158 Copper salts, 158... [Pg.704]

Dehydrooenation 1,4-Benzoquinone. Chloranil. o-Chloranil. Copper chromite. Copper-Chromium oxide. Diethyl azodicarboxylate. 2,3-Dichloro-3,6-dicyano-I,4-benzoquinone. DIphenylpIcrylhydrazyl, N-Lithioethylenediamlne. Mercuric acetate. Nickel catalyst. Oleic add, Palladium. Perbenmic acid. Potassium l-butoxide. Pyrldinium hydrobromide per-bramlda, Balinlum. Selenium dioxide. Sodium borohydride. Sulfdr (sm 1,2-Naphthalic anhydridli preparation). Tetracyanoethylene. Thionyl chloride. Trityl perchlorate. [Pg.1387]

Copper chromite has been made by the ignition of basic copper chromate at a red heat and by the thermal decomposition of copper ammonium chromate. The procedure given here is a modification of the latter method in which barium ammonium chromate is also incorporated. Copper-chromium oxide hydrogenation catalysts have also been prepared by grinding or heating together copper oxide and chromium oxides, by the decomposition of copper ammonium chromium carbonates... [Pg.18]


See other pages where Copper chromite Chromium oxide is mentioned: [Pg.41]    [Pg.26]    [Pg.872]    [Pg.872]    [Pg.153]    [Pg.872]    [Pg.249]    [Pg.89]    [Pg.102]    [Pg.89]    [Pg.52]    [Pg.354]    [Pg.192]    [Pg.438]    [Pg.872]    [Pg.48]   
See also in sourсe #XX -- [ Pg.26 ]




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Chromite

Chromium aluminum oxid Copper chromite)

Chromium oxidants

Chromium oxide

Chromium oxids

Chromium-copper

Copper oxidized

Oxidants copper

Oxidative coppering

Oxides chromium oxide

Oxidic copper

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