Gas-phase hydrogenation of acetonitrile over Pt and Pt-Pd supported on mesoporous solids:: influence of the metallic precursor

被引:27
作者
Carrión, MC
Manzano, BR
Jalón, FA
Fuentes-Perujo, I
Maireles-Torres, P
Rodríguez-Castellón, E
Jiménez-López, A
机构
[1] Univ Malaga, Fac Ciencias, Dept Quim Inorgan Cristalog & Mineral, E-29071 Malaga, Spain
[2] Univ Castilla La Mancha, Fac Quim, Dept Quim Inorgan Organ & Bioquim, E-13071 Ciudad Real, Spain
关键词
MCM-41; dinuclear complex; platinum; bimetallic catalyst; mesoporous solid; hydrogenation of acetonitrile;
D O I
10.1016/j.apcata.2005.03.042
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
Gas-phase hydrogenation of acetonitrile has been chosen as a test reaction to evaluate the catalytic behaviour of supported bimetallic catalysts prepared from dinuclear complexes precursors. Thus, Pd/Pt supported on zirconium doped mesoporous silica catalysts, with total metal loading of 1 and 2 wt.%, have been obtained by incipient wetness impregnation by using [PdPtCl2(mu-dppm)21, after removing the ligands by calcination and subsequent reduction with H-2. These catalysts have been compared with supported platinum or palladium/platinum catalysts with similar metal loadings prepared from classical inorganic salts ([Pt(NH3)(4)](NO3)(2), PdCl2 and H(2)PtCl(6)(.)6H(2)O). The metal-based catalysts have been characterized by powder XRD, adsorption-desorption of N-2 at 77 K, TEM, H-2-TPR and NH3-TPD. A remarkable high degree of metal dispersion was attained when using the dinuclear precursor, giving rise to the highest yield of triethylamine in the gas-phase hydrogenation of acetonitrile, with a selectivity toward this tertiary amine close to 100%. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:34 / 42
页数:9
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