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Catalytic oxidation of carbon monoxide over RuRh/SiO/sub 2/ bimetallic clusters

Journal Article · · J. Phys. Chem.; (United States)
DOI:https://doi.org/10.1021/j100276a029· OSTI ID:6038414
The oxidation of CO over a series of well-characterized Ru-Rh/SiO/sub 2/ catalysts has been studied both in a Pyrex microreactor and by using an in situ infrared cell-reactor. The incorporation of Rh into a supported Ru catalyst results in the formation of bimetallic clusters which have mixed metal surface sites. The incorporation of Rh into a supported Ru catalysts results in the formation of bimetallic clusters which have mixed metal surface sites. These bimetallic clusters are much more resistant to deactivation by oxygen than Ru/SiO/sub 2/. The ratio of CO/O/sub 2/ partial pressures required for a change over from a diffusion-controlled regime to a kinetically controlled regime increases from 1.0 on Rh/SiO/sub 2/ to 2.0 on Ru/SiO/sub 2/ at 100 /sup 0/C. This observation correlates well with an increase in the strength of the metal-oxygen bond for Ru as compared to Rh. In situ infrared spectra of adsorbed CO during reaction conditions show that the changeover between the diffusion-controlled and kinetically controlled regimes is concomitant with the displacement of an O/sub 2/ adlayer by CO. Turnover frequencies for the rate of CO/sub 2/ formation as a function of surface composition over the series of bimetallic clusters studied showed little or no synergism. 27 references, 7 figures, 3 tables.
Research Organization:
Univ. of Rhode Island, Kingston
OSTI ID:
6038414
Journal Information:
J. Phys. Chem.; (United States), Journal Name: J. Phys. Chem.; (United States) Vol. 90:4; ISSN JPCHA
Country of Publication:
United States
Language:
English