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Hydrogenation of Aliphatic Carboxylic Acids

Aliphatic aldehydes are also important intermediates for fine chemical manufacture. The Cr -modified catalyst, however, is not suitable for the preparation of these, because of its low selectivity [17]. [Pg.374]

Several commercially available Cr203 catalysts have been tested, affording quite different results for activity and selectivity (Table 4). Impurities in Cr203, especially alkali metals and alkaline earth metals, have a strong influence on catalytic performance. These contaminant impurities in Cr203 result in a drastic decrease in activity and selectivity, as has been reported elsewhere [17]. Selectivity is reduced mainly because of ketone formation. [Pg.374]

Catalyst Temperature rc) Conversion of acid (%) Selectivity (%) Total-UDEH Ketone 10-UDEH/ Total-UDEH [Pg.375]

4 Application of Cf203 Catalysts to Different Aliphatic Carboxylic Acids [Pg.376]


It is worth mentioning that cyclic acetal-type saccharide-based surfactants are promising not only with respect to their environmental properties but also as concerns their synthesis. Recently, the Mitsubishi Chemical Corporation elaborated and commercialized a process of direct hydrogenation of aliphatic carboxylic acids to the corresponding aldehydes [181,182]. This process allows long-chain aliphatic aldehydes to be obtained from natural fats and oils, and, as a consequence, to produce cyclic acetal-type saccharide surfactants entirely from renewable feedstock. [Pg.184]


See other pages where Hydrogenation of Aliphatic Carboxylic Acids is mentioned: [Pg.387]    [Pg.374]    [Pg.317]   


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Acidity aliphatic

Aliphatic carboxylic acids

Aliphatic hydrogenation

Aliphatics acidic hydrogen

Carboxylic acids aliphatic, acidity

Carboxylic acids hydrogenation

Carboxylic aliphatic

Hydrogen aliphatic

Hydrogen carboxylic acid

Hydrogenation of acids

Hydrogenation of carboxylic acids

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