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Infrared study on the formation of isocyanate in the NO and CO reaction on supported IR catalyst

Journal Article · · J. Catal.; (United States)
An infrared study on the formation of isocyanate in the NO + CO reaction on supported Ir catalyst was conducted to elucidate the mechanism of ammonia formation during catalytic treatment of automobile exhaust gases and to develop a new catalytic route for ammonium isocyanate and isocyanic acid. On reduced iridium supported on alumina, silica, titanium dioxide, or magnesium oxide, the isocyanate species (2260-2240 cm/sup -//sup 1/) formed above 200/sup 0/C, with maximum intensity at 280/sup 0/-300/sup 0/C, from gaseous mixtures of nitric oxide and carbon monoxide, and from preadsorbed nitric oxide and gaseous carbon monoxide, but not from preadsorbed carbon monoxide and gaseous nitric oxide. The isocyanate decomposed on evacuation above 300/sup 0/C with formation of carbon monoxide and dioxide and molecular nitrogen. Oxidized iridium had similar spectra of lower intensities. The location of the isocyanate band depended on the support. The results were consistent with a proposed mechanism which accounted for all products detected, and which indicated the dissociative adsorption of nitric oxide as the rate-determining step and migration of the NCO species formed on iridium to the metal of the support oxide.
Research Organization:
Univ. Szeged
OSTI ID:
6326021
Journal Information:
J. Catal.; (United States), Journal Name: J. Catal.; (United States) Vol. 63:1; ISSN JCTLA
Country of Publication:
United States
Language:
English