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Hydrogenation of adsorbed carbon monoxide on supported platinum group metals

Journal Article · · J. Catal.; (United States)
Hydrogenation of adsorbed carbon monoxide on supported platinum group metals was studied by in situ ir spectroscopy and reactive temperature-programmed desorption (RTD) methods using hydrogen as a carrier gas. The main product of the hydrogenation was methane. The RTD gave spectra for methane formation which showed peaks between 423 and 650 K depending on the metals. On alumina-supported metals the temperature of maximum methane formation was in the following order: Ru(420K) approx. = Rh(420K) < Pd(490 K) < Pt(560 K) < Ir (600 K). It agreed well with the order of catalytic activity for the hydrogenation of carbon monoxide, which had been referenced elsewhere. The ir spectra of the bridge, linear, and twin types of adsorbed CO were observed on Rh/Al/sub 2/O/sub 3/ or Ru/Al/sub 2/O/sub 3/. On both samples the bridge CO was hydrogenated at lower temperature than the linear CO to form hydrocarbons consisting mainly of methane. The twin CO on Rh/Al/sub 2/O/sub 3/ desorbed without being hydrogenated. Some adsorbed hydrocarbon species were observed on Ru/Al/sub 2/O/sub 3/ during hydrogenation. Adsorbed CO reacted easily with H/sub 2/O in the gas phase to form CO/sub 2/. 8 figures, 2 tables.
Research Organization:
Univ. of Tokyo, Japan
OSTI ID:
5448260
Journal Information:
J. Catal.; (United States), Journal Name: J. Catal.; (United States) Vol. 61:1; ISSN JCTLA
Country of Publication:
United States
Language:
English