Bimetallic Ru/Ni supported catalysts for the gas phase hydrogenation of acetonitrile

被引:51
|
作者
Braos-Garcia, P. [1 ]
Garcia-Sancho, C. [1 ]
Infantes-Molina, A. [1 ]
Rodriguez-Castellon, E. [1 ]
Jimenez-Lopez, A. [1 ]
机构
[1] Univ Malaga, Fac Ciencias, Dept Quim Inorgan Cristalog & Mineral, ICP CSIC,Unidad Asociada, E-29071 Malaga, Spain
关键词
Gas phase acetonitrile hydrogenation; Supported nickel-ruthenium bimetallic catalysts; Mesoporous silica; SBA-15; NICKEL-IRON CATALYSTS; LIQUID-PHASE; ELECTRONIC INTERACTIONS; NI/MG(AL)O CATALYSTS; RUTHENIUM CATALYSTS; MESOPOROUS SILICA; SURFACE-AREAS; H/D EXCHANGE; NI-RU; NITRILES;
D O I
10.1016/j.apcata.2010.03.061
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A family of bimetallic Ni-Ru catalysts supported on a mesoporous SBA-15 silica was prepared by conventional impregnation method, with constant metal molar loadings, but varying Ni/(Ni + Ru) atomic ratios. The corresponding Ni and Ru monometallic catalysts were also prepared for comparison. These catalysts were characterized by XRD, N-2 adsorption-desorption at -196 degrees C, TEM, XPS, H-2-TPR, chemisorption of H-2 at r.t., H-2-TPD and NH3-TPD techniques. Finally, they were also tested in the hydrogenation of acetonitrile reaction, in the gas phase and at atmospheric pressure. Acetonitrile conversion values depended on the Ni/(Ni + Ru) composition of the bimetallic catalysts. Ru-rich bimetallic catalysts exhibited acetonitrile conversion values higher than that of pure Ni one; thus, although selectivity patterns remained almost unchanged, primary amine yields were increased. These higher conversion values resulted as a consequence of enhanced specific activity of Ni atoms, attributable to a strong interaction between both metals, Ni and Ru, likely because NiRu alloy nanoparticles were formed. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:132 / 144
页数:13
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