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Deactivation of alumina-supported nickel and ruthenium catalysts by sulfur compounds

Journal Article · · J. Catal.; (United States)

Deactivation of alumina-supported nickel and ruthenium catalysts by sulfur compounds was studied by temperature-programmed desorption, temperature-programmed surface reaction, and in flow experiments of carbon monoxide and hydrogen on a commercial catalyst (G-65) containing 25% nickel on alumina (Ni/Al) and on this catalyst with 1% iridium added (Ni/Ir/Al) in the absence and presence of hydrogen sulfide. The Ni/Ir/Al catalyst adsorbed 30% more CO than Ni/Al, and it desorbed in three temperature peaks, compared with two desorption peaks for Ni/Al. Carbon dioxide and surface carbon were formed during the desorption. On Ni/Al, two types of surface carbon were formed with different reactivities towards hydrogen, and on Ni/Ir/Al only one highly reactive carbon species was detected. In the presence of hydrogen sulfide, adsorption decreased, less carbon was formed on Ni/Ir/Al and none on Ni/Al, and the methanation reaction decayed at a rate which was determined for the two catalysts. The iridium increased the sulfur resistance of the catalyst by a factor of two. An alumina-supported 5% ruthenium catalyst deactivated more rapidly than Ni/Al.

Research Organization:
SRI Int.
OSTI ID:
6420413
Journal Information:
J. Catal.; (United States), Journal Name: J. Catal.; (United States) Vol. 61:1; ISSN JCTLA
Country of Publication:
United States
Language:
English