Temperature-programmed sulfiding of precursor cobalt oxide genesis of highly active sites on sulfided cobalt catalyst for hydrogenation and isomerization
Journal Article
·
· Journal of Catalysis; (United States)
- Idemitsu Kosan Co. Ltd., Chiba (Japan)
- Osaka Univ. (Japan)
It was found that the method of sulfidation of cobalt oxide strongly affects the catalytic activities and selectivities of the resultant cobalt sulfide catalyst, as well as the calcination temperature of the cobalt oxide. When cobalt oxide was sulfided at 673 K by a temperature-programmed sulfiding method (a heating rate of 6 K/min), catalytic activities for the hydrogenation of butadiene and the isomerization of 1-butene were considerably enhanced compared with those for cobalt sulfide prepared by isothermal sulfidation at 673 K. Results of temperature-programmed sulfiding (TPS), temperature-programmed reduction (TPR), and X-ray diffraction (XRD) suggest that the catalysts showing high catalytic activities after sulfidation are partially sulfided at 673 K and consist of the unsulfided cobalt core phases (CoO or metallic Co). The sulfidation property of precursor cobalt oxides has been studied using TPS, simulating the sulfidation process of the cobalt sulfide catalysts. Two distinctly different kinds of sulfidation process are estimated by TPS measurements of the cobalt oxides. The calcination temperature of the precursor cobalt oxides strongly affects the sulfidation paths. They are differentiated in terms of the presence of a metallic Co intermediate. The relationship of the mechanism of sulfidation of the cobalt oxides to the generation of highly active sites is discussed.
- OSTI ID:
- 7161988
- Journal Information:
- Journal of Catalysis; (United States), Journal Name: Journal of Catalysis; (United States) Vol. 133:2; ISSN 0021-9517; ISSN JCTLA
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
02 PETROLEUM
020400 -- Petroleum-- Processing
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
400201* -- Chemical & Physicochemical Properties
ALKENES
BUTADIENE
BUTENES
CALCINATION
CATALYSTS
CATALYTIC EFFECTS
CHALCOGENIDES
CHEMICAL REACTION KINETICS
CHEMICAL REACTIONS
COBALT
COBALT COMPOUNDS
COBALT OXIDES
COBALT SULFIDES
COHERENT SCATTERING
CONTROL
CORRELATIONS
DECOMPOSITION
DIENES
DIFFRACTION
ELEMENTS
ENERGY SOURCES
FOSSIL FUELS
FUELS
HEATING RATE
HYDROCARBONS
HYDROGENATION
ISOMERIZATION
KINETICS
METALS
ORGANIC COMPOUNDS
OXIDES
OXYGEN COMPOUNDS
PETROLEUM
PHASE STUDIES
POLYENES
PYROLYSIS
REACTION KINETICS
REDUCTION
SCATTERING
SULFIDATION
SULFIDES
SULFUR COMPOUNDS
TEMPERATURE CONTROL
THERMOCHEMICAL PROCESSES
TRANSITION ELEMENT COMPOUNDS
TRANSITION ELEMENTS
X-RAY DIFFRACTION
020400 -- Petroleum-- Processing
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
400201* -- Chemical & Physicochemical Properties
ALKENES
BUTADIENE
BUTENES
CALCINATION
CATALYSTS
CATALYTIC EFFECTS
CHALCOGENIDES
CHEMICAL REACTION KINETICS
CHEMICAL REACTIONS
COBALT
COBALT COMPOUNDS
COBALT OXIDES
COBALT SULFIDES
COHERENT SCATTERING
CONTROL
CORRELATIONS
DECOMPOSITION
DIENES
DIFFRACTION
ELEMENTS
ENERGY SOURCES
FOSSIL FUELS
FUELS
HEATING RATE
HYDROCARBONS
HYDROGENATION
ISOMERIZATION
KINETICS
METALS
ORGANIC COMPOUNDS
OXIDES
OXYGEN COMPOUNDS
PETROLEUM
PHASE STUDIES
POLYENES
PYROLYSIS
REACTION KINETICS
REDUCTION
SCATTERING
SULFIDATION
SULFIDES
SULFUR COMPOUNDS
TEMPERATURE CONTROL
THERMOCHEMICAL PROCESSES
TRANSITION ELEMENT COMPOUNDS
TRANSITION ELEMENTS
X-RAY DIFFRACTION