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Reduction of NO by H/sub 2/-CO mixtures over silica-supported rhodium: infrared and kinetic studies

Journal Article · · J. Catal.; (United States)
OSTI ID:6387585

The kinetics of NO reduction by H/sub 2/-CO mixtures have been investigated over a Rh/SiO/sub 2/ catalyst. Nearly 90% of the reduction can be ascribed to H/sub 2/. The presence of CO retards the rate of NO reduction, presumably due to competitive adsorption with H/sub 2/. The formation of urea is a direct result of NO reduction by H/sub 2/ and CO. The catalyst activity is 50% higher when the catalyst is preoxidized rather than prereduced. N/sub 2/O, N/sub 2/, NH/sub 3/, and (NH/sub 2/)/sub 2/CO are formed over the prereduced catalyst. NH/sub 3/ formation is largely suppressed when the catalyst is preoxidized and a product believed to be HNCO is formed instead of urea. In situ infrared spectra of the catalyst show that for NO conversions below 70%, the surface is dominated by adsorbed NO. At higher conversions, bands are also observed for adsorbed CO, but none for isocyanate species attached to Rh.

Research Organization:
Univ. of California, Berkeley
OSTI ID:
6387585
Journal Information:
J. Catal.; (United States), Journal Name: J. Catal.; (United States) Vol. 88:2; ISSN JCTLA
Country of Publication:
United States
Language:
English