Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Chemisorption of hydrogen sulfide on nickel and ruthenium catalysts-1. Desorption isotherms

Journal Article · · J. Catal.; (United States)
Hydrogen adsorption isotherms at 25/sup 0/C, saturation sulfur uptake at 450/sup 0/C, and sulfur desorption into H/sub 2//H/sub 2/S at 450/sup 0/C were determined for the methanation catalysts alumina-supported 3% Ni, 10% Ni/10% Co, 16% Ni/0.5% Pt, and 0.5% Ru, and for unsupported Ni and Al/sub 2/O/sub 3/. The elution curves at 450/sup 0/C (and for Ni/Pt also at 520/sup 0/C) were measured as a function of 0.1-30 ppm H/sub 2/S in the hydrogen stream and of hydrogen flow rate, and the results transformed into H/sub 2/S desorption isotherms. The desorption isotherms followed a Langmuir equation. The heat of H/sub 2/S chemisorption on Ni/Pt was derived as 38 kcal/mole. The H/sub 2/S heat of adsorption on Ni was estimated as 30-40 kcal/mole at 50-90% coverage. An analysis of the results showed that H/sub 2/S chemisorption on Ni and Ru was very strong and that it was stronger on unsupported than supported nickel; that saturation coverage was lower on nickel alloys than on nickel and much lower on supported ruthenium than on nickel; and that H/sub 2/S adsorbed on nickel at 450/sup 0/C dissociatively up to monolayer coverage and molecularly at higher coverage and desorbed in the presence of 25-30 ppm H/sub 2/S to leave an Ni-S stoichiometric surface and in the presence of 8-12 ppm H/sub 2/S to form an Ni/sub 3/S/sub 2/ surface. Graphs, tables, and 31 references.
Research Organization:
Brigham Young Univ., Provo, Utah
OSTI ID:
5782480
Journal Information:
J. Catal.; (United States), Journal Name: J. Catal.; (United States) Vol. 51:2; ISSN JCTLA
Country of Publication:
United States
Language:
English