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Catalytic probe for alloy formation in supported PtRe catalysts: isotope exchange and hydrogenolysis of cyclopentane

Journal Article · · J. Catal.; (United States)
The H/D isotope exchange and the hydrogenolysis of cyclopentane (CP) as catalyzed by alumina- or silica-supported Pt, Re, their alloys, and physical mixtures have been studied. The number of surface-exposed metal atoms is determined by chemisorbing deuterium and exchanging it with hydrogen. The CP exchange reaction is found to be nonspecific for the composition of the catalyzing ensembles: PtRe alloys exhibit the same rate and exchange pattern as a physical mixture of these metals with the same number of metal atoms exposed. The exchange rate can therefore be used to count exposed metal atoms. The exchange patterns over Pt and PtRe show partial maxima for d/sub 5/ and d/sub 10/; over PtRe all products are formed in quantities intermediate to those obtained over Pt and Re respectively. CP hydrogenolysis is highly ensemble-specific. The TOF (turnover frequency) for methane formation over PtRe exceeds that over the separate metals by a factor of 40. This finding is used to estimate the extent of alloy formation in supported bimetallic PtRe catalysts. Even in physical mixtures of Pt and Re, initially supported on separated support particles, some alloy formation can be detected.
Research Organization:
Northwestern Univ., Evanston, IL (USA)
OSTI ID:
5204285
Journal Information:
J. Catal.; (United States), Journal Name: J. Catal.; (United States) Vol. 106:2; ISSN JCTLA
Country of Publication:
United States
Language:
English