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Methanation and HDS catalysts based on sulfided, bimetallic clusters

Conference · · Prepr. Pap., Am. Chem. Soc., Div. Fuel Chem.; (United States)
OSTI ID:6888265
Environmental concerns have led to an increased interest in hydrotreating catalysts, i.e. catalysts for hydrodesulfurization (HDS) or hydrodenitrogenation (HDN). Although HDS may be catalyzed by bulk or supported MoS/sub 2/ and related sulfides, the most effective catalysts are those derived from ''sulfided cobalt molybdate'' supported on Al/sub 2/O/sub 3/. These catalysts are prepared conventionally by impregnating the alumina support with solutions of molybdate ions and cobaltous ions. The impregnated support is then calcined to convert the adsorbed species to their respective oxides. The supported metal oxides are then converted to sulfides (''sulfided'') with a mixture of H/sub 2/ and H/sub 2/S (or the feed stream itself) at temperatures in the range 300-400/sup 0/C. Alternate promoters, e.g. Ni and Fe, may be used in the place of Co, but the resulting catalysts usually show a lower activity. Despite intensive study, the exact nature of the active ''CoMoS'' phase is still uncertain, and hence the role of the Co promoter and the exact mechanism of HDS remain obscure. XPS and Mossbauer Emission Spectroscopy has been used to show that a ''CoMoS'' phase, distinct from Co/sub 9/S/sub 8/ or MoS/sub 2/, is present and that the activity of the catalyst parallels the amount of this CoMoS phase present. More recently, EXAFS has been used to study these cobalt molybdate catalysts in both the oxidized and sulfided states.
Research Organization:
Departments of Chemistry and Chemical Engineering, The Univ. of Michigan, Ann Arbor, MI 48109
OSTI ID:
6888265
Report Number(s):
CONF-8609181-
Conference Information:
Journal Name: Prepr. Pap., Am. Chem. Soc., Div. Fuel Chem.; (United States) Journal Volume: 31:3
Country of Publication:
United States
Language:
English

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