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Dehydrogenation and hydrogenation activity of palladium-tin-silica and nickel-tin silica

Journal Article · · J. Catal.; (United States)
The dehydrogenation of cyclohexanone on palladium-tin-silica catalyst at 753/sup o/K yielded phenol as major product; the dehydrogenation of cyclohexylamine at 673/sup o/K yielded mainly aniline; the dehydrogenation of 2-propanol at 723/sup o/K yielded only acetone; the dehydrogenation of cyclohexane at 723 yielded only benzene. The optimum dehydrogenation catalyst had a 3:1 palladium-tin ratio for cyclohexylamine and cyclohexane and a 0.3:1 ratio for cyclohexanone and 2-propanol, and all four conversions were higher with, than without tin. The hydrogenation of ethylene on palladium-tin-silica yielded only ethane, and conversions were higher on 100% Pd than on palladium/tin catalysts. The hydrogenation of benzene on nickel/tin/silica yielded only cyclohexane and conversions were higher on nickel/silica than on this catalyst with added tin. These results, and carbon monoxide adsorption studies, carbon deposition, X-ray diffraction patterns, and ESCA studies suggested that the tin causes a weakening of the adsorption bond, and prevents formation of deposits which poison dehydrogenation and promote hydrogenation. Graphs, spectra, tables, and 25 references.
Research Organization:
Kobe Univ., Japan
OSTI ID:
5709475
Journal Information:
J. Catal.; (United States), Journal Name: J. Catal.; (United States) Vol. 50:3; ISSN JCTLA
Country of Publication:
United States
Language:
English