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Title: Kinetic studies of the water gas shift reaction on a sulfided cobalt/molybdena/alumina catalyst

Thesis/Dissertation ·
OSTI ID:7019276

In this study, the applicability of low temperature oxygen chemisorption (LTOC) to measure the specific surface area of several rare-earth oxides (La, Ce, Pr, Nd, Tb) and the kinetics of the water-gas shift reaction over a sulfided cobalt-molybdena-alumina (AMOCAT 1A) catalyst are investigated. The LTOC results indicate that oxygen is possibly adsorbed in the molecular form, O/sub 2//sup -/, as observed by others after heat treatment of these oxides in vacuum. Lanthana and ceria were found to have ratios of total surface area to LTOC similar to those of chromia and molybdena respectively, after a comparable pretreatment. Furthermore, ceria is deduced to exist as a monolayer on the alumina support at loadings below 12%. An additional hour of reduction after the 6 hours of reduction shows a significant increase in LTOC on lanthana, neodymia and terbia which may be due to phase changes exhibited by these polymorphic oxides. The kinetics of the water-gas shift reaction has been extensively studied on iron oxide (high temperature shift) and copper oxide (low temperature shift) based catalysts. This investigation establishes the kinetics over a sulfided cobalt-molybdena-alumina (AMOCAT 1A) catalyst in the medium temperature shift range, 250-300/sup 0/C. The catalyst was sulfided in-situ in a high pressure integrated Berty reactor system. Reaction rates were measured for different CO/H/sub 2/O feed ratios in the range 0.3-3.0, with and without CO/sub 2/ in the feed. The reaction was carried out at several pressures in the range 5-27 atm. and GHSV's in the range 4800-2400 hr/sup 1/.

Research Organization:
State Univ. of New York, Buffalo (USA)
OSTI ID:
7019276
Resource Relation:
Other Information: Thesis (Ph. D.)
Country of Publication:
United States
Language:
English