Chemically modified cyclodextrins as supramolecular tools to generate carbon-supported ruthenium nanoparticles: An application towards gas phase hydrogenation

被引:21
|
作者
Wyrwalski, F. [1 ,2 ,4 ]
Leger, B. [1 ,2 ,4 ]
Lancelot, C. [2 ,3 ,4 ]
Roucoux, A. [5 ,6 ]
Monflier, E. [1 ,2 ,4 ]
Ponchel, A. [1 ,2 ,4 ]
机构
[1] UArtois, UCCS, F-62300 Lens, France
[2] Univ Lille Nord France, F-59000 Lille, France
[3] USTL, UCCS, F-59650 Villeneuve Dascq, France
[4] CNRS, UMR 8181, F-75700 Paris, France
[5] Ecole Natl Super Chim Rennes, CNRS, UMR 6226, CS 50837, F-35708 Rennes 7, France
[6] Univ Europeenne Bretagne, Rennes, France
关键词
Cyclodextrins; Metallic nanoparticles; Activated carbon; Hydrogenation; Gas phase reactions; O-XYLENE HYDROGENATION; PALLADIUM NANOPARTICLES; BETA-CYCLODEXTRIN; METHYLATED CYCLODEXTRINS; RECYCLABLE CATALYSTS; POLYOL PROCESS; NANOCATALYST; DISPERSIONS; COMPLEXES; BEHAVIOR;
D O I
10.1016/j.apcata.2010.07.006
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 series of carbon-supported ruthenium catalysts was synthesized from zerovalent ruthenium nanoparticles stabilized by randomly methylated cyclodextrins (alpha-, beta- and gamma-CD) followed by their adsorption onto the carbon support. The catalysts were characterized by N-2 physisorption and thermal analyses. The deposited ruthenium nanoparticles were characterized by transmission electron microscopy, which has highlighted predominantly spherical shapes with a mean diameter of 2.4 nm. Catalytic activity was investigated in the gas phase hydrogenation of o-, m- and p-xylene at 85 degrees C, both separately and in a two-component mixture (o- and p-xylene). The catalyst prepared by a 1:3 concentration ratio of RuCl3 to randomly methylated beta-cyclodextrin exhibited the highest hydrogenation activity and stereoselectivity toward the formation of trans-dimethylcyclohexane. The beta-cyclodextrin appeared as multifunctional molecular receptors enabling the stabilization and dispersion of the metallic nanoparticles onto the support and the promotion of the catalytic reaction through host-guest interactions. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:334 / 341
页数:8
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