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Selective hydrogenation of nitrostyrene to aminostyrene over Pt/TiO2 catalysts : Effects of pressurized carbon dioxide and catalyst preparation conditions

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Title: Selective hydrogenation of nitrostyrene to aminostyrene over Pt/TiO2 catalysts : Effects of pressurized carbon dioxide and catalyst preparation conditions
Authors: Fujita, Shin-ichiro Browse this author →KAKEN DB
Yoshida, Hiroshi Browse this author →KAKEN DB
Asai, Kouki Browse this author
Meng, Xiangchun Browse this author
Arai, Masahiko Browse this author →KAKEN DB
Keywords: Carbon dioxide
Hydrogenation
Platinum catalyst
Molecular interaction
SMSI
Issue Date: Dec-2011
Publisher: Elsevier B.V.
Journal Title: The Journal of Supercritical Fluids
Volume: 60
Start Page: 106
End Page: 112
Publisher DOI: 10.1016/j.supflu.2011.02.016
Abstract: The present work has studied the influence of CO2 pressurization on the hydrogenation of nitrostyrene (NS) using Pt/TiO2. With CO2 pressurization up to 12 MPa (CO2-dissolved expanded liquid (CXL) phase), the over-all reaction rate and the selectivity to aminostyrene (AS) increased. At higher CO2 pressures where all NB dissolved in scCO2 (scCO2-homogeneous phase), both of them decreased with increasing the CO2 pressure. The phase behavior was an important factor for the present reaction system. It was also found that the presence of pressurized CO2 gave higher selectivity to AS than in its absence at any conversion level. This was ascribed to retardation effects of dense phase CO2 on the hydrogenation of AS to ethylaniline. Competitive adsorption of nitro and vinyl groups was suggested to determine the product selectivity. FTIR measurements showed that the pressurized CO2 lowers the reactivity of the nitro group, and this effect is stronger in scCO2-homogeneous phase than in CXL phase, resulting in the lower AS selectivity in the former phase. Lower Pt loadings and higher catalyst reduction temperatures gave Pt/TiO2 catalysts more selective for the AS formation. FTIR measurements of adsorbed CO over the catalysts suggested that the presence of less-coordinated Pt atoms on edge, corner and kink sites was significant for the selective hydrogenation of NS to AS.
Type: article (author version)
URI: http://hdl.handle.net/2115/48154
Appears in Collections:工学院・工学研究院 (Graduate School of Engineering / Faculty of Engineering) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 荒井 正彦

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