X-ray photoelectron spectroscopic characterization of MoO/sub 3//SiO/sub 2/ hydrodesulfurization catalysts
Journal Article
·
· J. Phys. Chem.; (United States)
An x-ray photoelectron spectroscopic study of MoO/sub 3//SiO/sub 2/ hydrodesulfurization catalysts was carried out to understand their physiochemical and catalytic behavior and to compare the results with a previous study of MoO/sub 3//Al/sub 2/O/sub 3/ catalysts. With the oxidic MoO/sub 3//SiO/sub 2/ catalysts, it was found that Mo was well dispersed to form monolayers below 2 wt % MoO/sub 3/ content (ca. 0.4 x 10/sup 18/ Mo atoms/m/sup 2/), compared to ca. 13 wt % MoO/sub 3/ (4 x 10/sup 18/ Mo atoms/m/sup 2/) for alumina-supported catalysts. Multilayered Mo species and microcrystalline MoO/sub 3/ developed as the MoO/sub 3/ content increased to ca. 9 wt %. Above 13 wt % MoO/sub 3/, crystalline MoO/sub 3/ was detected by XRD. At high MoO/sub 3/ content, no Mo species interacting strongly with SiO/sub 2/ was observed by XPS. When sulfided, MoO/sub 3//SiO/sub 2/ catalysts were characterized by more vigorous surface segregations and subsequent sinterings of Mo and by lower degrees of Mo sulfidation, compared to those for MoO/sub 3//Al/sub 2/O/sub 3/ catalysts, except for the extremely low MoO/sub 3/ content catalysts. It was found that the extent of the sulfidation of Mo was restricted within the formation of double layers of a two-dimensional MoS/sub 2/ layer over MoO/sub 2/ at atmospheric pressure and within the formation of double layers of a two-dimensional MoS/sub 2/ layer over MoO/sub 2/ at atmospheric pressure and 400/sup 0/C. The discrepancies in the physiochemical and catalytic features between SiO/sub 2/..mu.. and Al/sub 2/O/sub 3/-supported catalysts are well understood in terms of the strength of Mo-support interactions and resultant Mo species on sulfidation. Differential charging effects in the XPS measurements are pointed out to be very important for the interpretations of the XPS results on MoO/sub 3//SiO/sub 2/ catalysts.
- Research Organization:
- Osaka Univ., Japan
- OSTI ID:
- 5590095
- Journal Information:
- J. Phys. Chem.; (United States), Journal Name: J. Phys. Chem.; (United States) Vol. 85:25; ISSN JPCHA
- Country of Publication:
- United States
- Language:
- English
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Journal Article
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Thu Jul 10 00:00:00 EDT 1980
· J. Phys. Chem.; (United States)
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OSTI ID:5130331
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Mon Aug 01 00:00:00 EDT 1988
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Journal Article
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Mon Jun 01 00:00:00 EDT 1987
· J. Catal.; (United States)
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Related Subjects
01 COAL, LIGNITE, AND PEAT
010402 -- Coal
Lignite
& Peat-- Purification & Upgrading
02 PETROLEUM
020400 -- Petroleum-- Processing
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
400201* -- Chemical & Physicochemical Properties
BINDING ENERGY
CATALYSTS
CATALYTIC EFFECTS
CHALCOGENIDES
CHEMICAL REACTIONS
DATA
DESULFURIZATION
ELECTRON SPECTROSCOPY
ENERGY
EXPERIMENTAL DATA
HYDROGENATION
INFORMATION
MOLYBDENUM COMPOUNDS
MOLYBDENUM OXIDES
NUMERICAL DATA
OXIDES
OXYGEN COMPOUNDS
PHOTOELECTRON SPECTROSCOPY
SILICON COMPOUNDS
SILICON OXIDES
SPECTROSCOPY
TRANSITION ELEMENT COMPOUNDS
X-RAY SPECTROSCOPY
010402 -- Coal
Lignite
& Peat-- Purification & Upgrading
02 PETROLEUM
020400 -- Petroleum-- Processing
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
400201* -- Chemical & Physicochemical Properties
BINDING ENERGY
CATALYSTS
CATALYTIC EFFECTS
CHALCOGENIDES
CHEMICAL REACTIONS
DATA
DESULFURIZATION
ELECTRON SPECTROSCOPY
ENERGY
EXPERIMENTAL DATA
HYDROGENATION
INFORMATION
MOLYBDENUM COMPOUNDS
MOLYBDENUM OXIDES
NUMERICAL DATA
OXIDES
OXYGEN COMPOUNDS
PHOTOELECTRON SPECTROSCOPY
SILICON COMPOUNDS
SILICON OXIDES
SPECTROSCOPY
TRANSITION ELEMENT COMPOUNDS
X-RAY SPECTROSCOPY