X-ray Photoelectron Spectroscopy Study of Mo-Ni/ gamma -Al sub(2)O sub(3) Catalysts for Hydroconversion of Fatty Oil Derivatives
The chemical states of Mo and Ni supported on gamma -Al sub(2)O sub(3) prepared under various conditions were investigated using X-ray photoelectron spectroscopy. The Mo species interacted with the Ni species interacting weakly with the support by co-impregnation of both the metal species to form Ni...
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Published in | Arabian Journal for Science and Engineering Vol. 39; no. 9; pp. 6617 - 6625 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
01.09.2014
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Online Access | Get full text |
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Summary: | The chemical states of Mo and Ni supported on gamma -Al sub(2)O sub(3) prepared under various conditions were investigated using X-ray photoelectron spectroscopy. The Mo species interacted with the Ni species interacting weakly with the support by co-impregnation of both the metal species to form Ni-Mo-O binary oxides. Increasing hydrogen pressure during pretreatment of the catalysts led to the formation of Ni-Mo-O binary oxides consisting of the metal species with a lower oxidation number, while the interaction between the two metal species was retained. By contrast, the strong Ni interaction with the support remained independent of the hydrogen pressure. In the hydroconversion of methyl laurate on Mo-Ni/ gamma -Al sub(2)O sub(3), the Mo species with a higher oxidation number in the binary oxide contributed to the formation of C sub(12) hydrocarbons, while the reduced Ni species and the Mo species with the lower oxidation number in the binary oxide promoted the formation of C sub(11) hydrocarbons. The strong interaction of the Mo species with the Ni species suppressed catalytic activity derived from the Ni species; however, that played an important role in the selective production of hydrocarbons with jet fuel fractions. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-2 |
ISSN: | 1319-8025 2191-4281 |
DOI: | 10.1007/s13369-014-1182-8 |