Influence of particles alloying on the performances of Pt-Ru/CNT catalysts for selective hydrogenation

被引:80
|
作者
Teddy, Jacques [1 ]
Falqui, Andrea [2 ]
Corrias, Anna [3 ]
Carta, Daniela [3 ]
Lecante, Pierre [4 ]
Gerber, Iann [5 ]
Serp, Philippe [1 ]
机构
[1] Univ Toulouse UPS INP LCC, Chim Coordinat Lab, UPR CNRS 8241, Composante ENSIACET, F-31432 Toulouse 4, France
[2] Ist Italiano Tecnol, I-16163 Genoa, Italy
[3] Univ Cagliari, Dipartimento Sci Chim, I-09042 Cagliari, Italy
[4] CNRS, Ctr Elaborat Mat & Etud Struct, F-31055 Toulouse, France
[5] Univ Toulouse INSA, UPS, LPCNO, IRSAMC, F-31077 Toulouse, France
关键词
Carbon nanotubes; Bimetallic catalysts; Selective hydrogenation; Platinum-ruthenium; NANOFIBER-SUPPORTED PLATINUM; AUGMENTED-WAVE METHOD; ALPHA; BETA-UNSATURATED ALDEHYDES; CARBON NANOTUBES; UNSATURATED ALDEHYDES; SURFACE-CHEMISTRY; CINNAMYL ALCOHOL; CINNAMALDEHYDE; ADSORPTION; NANOPARTICLES;
D O I
10.1016/j.jcat.2010.11.016
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
The influence of PtRu bimetallic particle size and composition on cinnamaldehyde selective hydrogenation has been investigated for the first time using well-defined catalysts based on carbon nanotubes support. Very high selectivity towards cinnamyl alcohol together with high activity have been obtained provided a high temperature treatment of the catalyst is performed. HRTEM, WAXS and EXAFS analyses permit us to conclude that the remarkable influence of this high temperature treatment on both activity and selectivity arises from different phenomena. First, a particle size and a structural effect have been evidence that permits to increase the selectivity. WAXS and EXAFS point the formation of alloyed PtRu nanoparticles. Second, the heat treatment allows the removal of oxygenated groups from CNT surface. This may increase the cinnamaldehyde adsorption capacity and decrease the activation barrier for diffusion of substrate and product on the CNT surface, thus contributing to an increase in the activity. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:59 / 70
页数:12
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