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Chromium oxides acids

It difiers from the cof per. chromium oxide catalyst described in Section VI,6 in that it has not been extracted with 10 per cent, acetic acid—a process which presumably removes some copper oxide. [Pg.321]

This preparation illustrates the use of the copper-chromium oxide catalyst in the r uotion of esters of dibasic acids to glycols ... [Pg.873]

Other catalysts that can be used are boron trifluoride (5), copper—chromium oxides (6), phosphoric acid (7), and siUca-alurnina (8). Under similar conditions, ethanol yields /V-ethylaniline [103-69-5] and /V,/V-diethylaniline [91-66-7] (9,10). [Pg.229]

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]

An autoclave (Note 1) is charged with 200 g. (1.28 moles) of 2,3-dimethylnaphthalene (Note 2), 940 g. (3.14 moles, 23% excess) of sodium dichromate dihydrate, and 1.8 1. of water. The autoclave is closed, heated to 250°, and shaken continuously at this temperature for 18 hours. The autoclave is cooled with continued agitation (Note 3), the pressure is released, and the autoclave is opened. The contents are transferred to a large vessel (Note 4). To effect complete transfer, the autoclave is rinsed with several 500-ml. portions of hot water. Green hydrated chromium oxide in the reaction mixture is separated on a large Buchner funnel and washed with warm water until the filtrate is colorless. The combined filtrates (7-8 1.) are acidified with 1.3 1. of 6N hydrochloric acid. The acidified mixture is allowed to... [Pg.80]

Hydrogenation of Fatty Acid Methyl Esters The hydrogenolysis of fatty acid methyl esters into the corresponding fatty alcohols and methanol is performed at 200-300°C and a H2 pressure of 200-300 bar with the aid of copper oxide/chromium oxide catalysts (Adkins catalysts). Three different procedures are applied [39 a-c] ... [Pg.20]

The pattern of oxidation states correlates with the pattern of acid-base behavior of d-metal oxides. Although most d-metal oxides are basic, the oxides of a given element show a shift toward acidic character with increasing oxidation number, just as the oxoacids do (recall Section 10.10). The family of chromium oxides is a good... [Pg.780]

Chemical Resistance. The chemical resistance of chromium carbide is superior to that of other interstitial carbides. Oxidation in air starts at 1000°C and a dense and strong oxide layer is formed. It is insoluble in cold HCl but dissolves in hot oxidizing acids. [Pg.237]

Some more recent processes have been developed which involve direct hydrogenation of the oil to the fatty acid and 1,2-propane diol. These high-temperature (>230 °C) and high-pressure processes generally use a copper chromium oxide catalyst. [Pg.187]

The fluorination of CF3CH2CI into CF3CH2F over chromium oxides is accompanied by a dehydrofluorination reaction (formation mainly of CF2=CHC1). This dehydrofluorination is responsible for the deactivation of the catalyst. A study of the dehydrofluorination reaction of CF3CH2CI proves that the reaction is favoured when the degree of fluorination of chromium oxide increases. Consequently it would be favoured on strong acid sites. Adding nickel to chromium oxide decreases the formation of alkenes and increases the selectivity for fluorination while the total activity decreases. Two kinds of active sites would be present at the catalyst surface. The one would be active for both the reactions of dehydrofluorination and of fluorination, the other only for the fluorination reaction. [Pg.379]

The fluorination of chromium oxide caused an increase of surface site Lewis acidity. Kemnitz and al.[12] as well as Peri [13], showed that on fluorinated alumina the progressive substitution of F for O and OH led, thanks to inductive attracting effect of fluorine, to an increase of the Lewis acidity of a sites. Hence the dehydrofluorination reaction was ftivoured on strong acide sites. [Pg.384]

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]

More than three decades ago, skeletal rearrangement processes using alkane or cycloalkane reactants were observed on platinum/charcoal catalysts (105) inasmuch as the charcoal support is inert, this can be taken as probably the first demonstration of the activity of metallic platinum as a catalyst for this type of reaction. At about the same time, similar types of catalytic conversions over chromium oxide catalysts were discovered (106, 107). Distinct from these reactions was the use of various types of acidic catalysts (including the well-known silica-alumina) for effecting skeletal reactions via carbonium ion mechanisms, and these led... [Pg.25]

A wide range of nonacidic metal oxides have been examined as catalysts for aromatization and skeletal isomerization. From a mechanistic point of view, chromium oxide catalysts have been, by far, the most thoroughly studied. Reactions over chromium oxide have been carried out either over the pure oxide, or over a catalyst consisting of chromium oxide supported on a carrier, usually alumina. Depending on its history, the alumina can have an acidic function, so that the catalyst as a whole then has a duel function character. However, in this section, we propose only briefly to outline, for comparison with the metal catalyzed reactions described in previous sections, those reactions where the acidic catalyst function is negligible. [Pg.81]

Jones reagent is prepared by dissolving chromium oxide (C1O3) (23.5 g) in coned sulfuric acid (21 mL) with cooling and then diluting with distilled water to give a total volume of 175 mL.4... [Pg.256]


See other pages where Chromium oxides acids is mentioned: [Pg.98]    [Pg.260]    [Pg.872]    [Pg.920]    [Pg.99]    [Pg.6]    [Pg.14]    [Pg.218]    [Pg.399]    [Pg.141]    [Pg.150]    [Pg.913]    [Pg.139]    [Pg.378]    [Pg.548]    [Pg.880]    [Pg.741]    [Pg.20]    [Pg.71]    [Pg.314]    [Pg.192]    [Pg.150]    [Pg.155]    [Pg.872]    [Pg.156]    [Pg.53]    [Pg.54]   
See also in sourсe #XX -- [ Pg.137 , Pg.195 ]




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Chromium oxidants

Chromium oxide

Chromium oxids

Oxides chromium oxide

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