Characterization of the active phase of NiMo/Al2O3 hydrodesulfurization catalysts

Authors
Hong, Seung TaePark, Dal RyungYoo, Seung-JoonKim, Jae-DuckPark, Hyung Sang
Issue Date
2006-12
Publisher
VSP BV
Citation
RESEARCH ON CHEMICAL INTERMEDIATES, v.32, no.9, pp.857 - 870
Abstract
The active phase of the NiMo/Al2O3 catalyst for hydrodesulfurization reactions has been investigated in this work. Special attention has been focused on the effect of the order of metal impregnation on the formation of the active phase in the reaction. The Mo and Ni oxides and their sulfides on the alumina were investigated by XPS and DRS analyses. The Ni-Mo oxides or precursor of the active phase which are chemically bonded between Mo and Ni were also confirmed from the binding energy shifts of the XPS peaks. The amount of Ni-Mo oxides was determined after the formation of metal oxides during calcination. The Ni-Mo sulfide (active phase) was then induced through sulfidation. It was important that Mo should be located at the tetrahedral sites on the alumina with a high Mo dispersion. These results indicated that there are two important factors in preparing highly efficient Ni-Mo catalysts; one is that Mo should be located at the tetrahedral coordination on Al2O3 in high dispersion (Mo/Al2O3) and the other is that the Ni species should be supported on MoAl2O4 to form Ni-Mo oxides which change into the Ni-Mo sulfide active sites by sulfidation.
Keywords
MOSSBAUER EMISSION-SPECTROSCOPY; MOLYBDENA-ALUMINA CATALYSTS; TEMPERATURE-PROGRAMMED REDUCTION; CO-MO CATALYSTS; SUPPORTED CO; NO ADSORPTION; S PHASE; SURFACE; HYDROGENATION; REDUCIBILITY; MOSSBAUER EMISSION-SPECTROSCOPY; MOLYBDENA-ALUMINA CATALYSTS; TEMPERATURE-PROGRAMMED REDUCTION; CO-MO CATALYSTS; SUPPORTED CO; NO ADSORPTION; S PHASE; SURFACE; HYDROGENATION; REDUCIBILITY; hydrodesulfurization; active phase; binding energy shift; XPS; DRS; tetrahedral Mo; NiO; impregnation order
ISSN
0922-6168
URI
https://pubs.kist.re.kr/handle/201004/134870
DOI
10.1163/156856706778938473
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KIST Article > 2006
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