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Reaction of alkanes and cycloalkanes on silica-supported platinum and platinum/gold alloy systems

Journal Article · · J. Catal.; (United States)
OSTI ID:6462381

Aerosil 200 supported 10% Pt/Au catalysts of 4% loading were prepared and calcined in air at 700/sup 0/C for 12 hr prior to reduction in order to obtain bulk metal homogeneity. Detailed product distributions were obtained in a flow reactor for the reactions of n-pentane with hydrogen at 340/sup 0/-400/sup 0/C, cyclopentane with hydrogen at 340/sup 0/-370/sup 0/C, methylcyclopentane with hydrogen at 340/sup 0/-450/sup 0/C, and ethane with hydrogen at 500/sup 0/C, and the results compared with the results obtained over silica-supported platinum under identical conditions. Hydrogen adsorption indicated that the alloy catalysts had < 0.4% surface platinum content. The alloy catalyst had good activity for bond-shift isomerization but not cyclization of n-pentane and was inactive for benzene formation from n-hexane, which differed from published data for Pt/Au films. It was also inactive for the hydrogenolysis of neopentane and ethane, and for ring opening of cyclopentane. The absence of 1,5-cyclization activity and possibly the high bond-shift activity were apparently a result of the surface topography, i.e., the relative extents of exposed crystal faces due to the severe heat treatment. The bond shift activity suggested a single-site mechanism.

OSTI ID:
6462381
Journal Information:
J. Catal.; (United States), Journal Name: J. Catal.; (United States) Vol. 64:1; ISSN JCTLA
Country of Publication:
United States
Language:
English