Synthesis and Characterization of Ferromagnetic Nickel–Cobalt Silicide Catalysts with Good Sulfur Tolerance in Hydrodesulfurization of Dibenzothiophene

Preparation of highly active and excellent sulfur tolerant hydrodesulfurization (HDS) catalysts is very important for the removal the sulfur from the sulfur containing compounds in petroleum. Herein we report on the synthesis and characterization of ferromagnetic nickel–cobalt silicide (Ni1–x Co x S...

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Veröffentlicht in:Journal of physical chemistry. C 2012-11, Vol.116 (47), p.24968-24976
Hauptverfasser: Chen, Xiao, Wang, Xinkui, Xiu, Jinghai, Williams, Christopher T, Liang, Changhai
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container_end_page 24976
container_issue 47
container_start_page 24968
container_title Journal of physical chemistry. C
container_volume 116
creator Chen, Xiao
Wang, Xinkui
Xiu, Jinghai
Williams, Christopher T
Liang, Changhai
description Preparation of highly active and excellent sulfur tolerant hydrodesulfurization (HDS) catalysts is very important for the removal the sulfur from the sulfur containing compounds in petroleum. Herein we report on the synthesis and characterization of ferromagnetic nickel–cobalt silicide (Ni1–x Co x Si2) solid solution catalysts having large surface area by the reaction of nickel cobalt oxide solid solutions with SiH4. The catalytic properties of Ni1–x Co x Si2 were investigated for HDS of dibenzothiophene (DBT). The results showed that the saturation magnetization of the Ni1–x Co x Si2 solid solutions with fluorite structure can be controlled by changing the molar ratio of Ni to Co. The nickel-rich Ni0.75Co0.25Si2 catalyst is much more active than that of monometallic silicide (NiSi2 and CoSi2) and significantly improves the hydrogenation property (31.5% HYD selectivity), proving the synergistic effect between the components. X-ray photoelectron spectroscopy (XPS) provided further evidence that the valence electron concentration of the Ni increased with increasing the Co substitution, enhancing the metal–silicon and metal–metal interactions. In addition, the Si sites in the silicides alter the metal coordination, leading to a strong modification of the electronic structure around the Fermi level of the metals. This engenders a high activity for the HDS of DBT and weakens the metal–sulfur bonds, improving the sulfur tolerance.
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Herein we report on the synthesis and characterization of ferromagnetic nickel–cobalt silicide (Ni1–x Co x Si2) solid solution catalysts having large surface area by the reaction of nickel cobalt oxide solid solutions with SiH4. The catalytic properties of Ni1–x Co x Si2 were investigated for HDS of dibenzothiophene (DBT). The results showed that the saturation magnetization of the Ni1–x Co x Si2 solid solutions with fluorite structure can be controlled by changing the molar ratio of Ni to Co. The nickel-rich Ni0.75Co0.25Si2 catalyst is much more active than that of monometallic silicide (NiSi2 and CoSi2) and significantly improves the hydrogenation property (31.5% HYD selectivity), proving the synergistic effect between the components. X-ray photoelectron spectroscopy (XPS) provided further evidence that the valence electron concentration of the Ni increased with increasing the Co substitution, enhancing the metal–silicon and metal–metal interactions. 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X-ray photoelectron spectroscopy (XPS) provided further evidence that the valence electron concentration of the Ni increased with increasing the Co substitution, enhancing the metal–silicon and metal–metal interactions. In addition, the Si sites in the silicides alter the metal coordination, leading to a strong modification of the electronic structure around the Fermi level of the metals. 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Herein we report on the synthesis and characterization of ferromagnetic nickel–cobalt silicide (Ni1–x Co x Si2) solid solution catalysts having large surface area by the reaction of nickel cobalt oxide solid solutions with SiH4. The catalytic properties of Ni1–x Co x Si2 were investigated for HDS of dibenzothiophene (DBT). The results showed that the saturation magnetization of the Ni1–x Co x Si2 solid solutions with fluorite structure can be controlled by changing the molar ratio of Ni to Co. The nickel-rich Ni0.75Co0.25Si2 catalyst is much more active than that of monometallic silicide (NiSi2 and CoSi2) and significantly improves the hydrogenation property (31.5% HYD selectivity), proving the synergistic effect between the components. X-ray photoelectron spectroscopy (XPS) provided further evidence that the valence electron concentration of the Ni increased with increasing the Co substitution, enhancing the metal–silicon and metal–metal interactions. In addition, the Si sites in the silicides alter the metal coordination, leading to a strong modification of the electronic structure around the Fermi level of the metals. This engenders a high activity for the HDS of DBT and weakens the metal–sulfur bonds, improving the sulfur tolerance.</abstract><cop>Columbus, OH</cop><pub>American Chemical Society</pub><doi>10.1021/jp308371y</doi><tpages>9</tpages></addata></record>
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source American Chemical Society Journals
subjects Catalysis
Catalysts: preparations and properties
Chemistry
Condensed matter: electronic structure, electrical, magnetic, and optical properties
Exact sciences and technology
General and physical chemistry
Magnetic properties and materials
Other ferromagnetic metals and alloys
Physics
Studies of specific magnetic materials
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
title Synthesis and Characterization of Ferromagnetic Nickel–Cobalt Silicide Catalysts with Good Sulfur Tolerance in Hydrodesulfurization of Dibenzothiophene
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