Ruthenium nanoparticles loaded on multiwalled carbon nanotubes for liquid-phase hydrogenation of fine chemicals: An exploration of confinement effect

被引:87
作者
Wang, Yong [1 ]
Rong, Zeming [1 ]
Wang, Yu [1 ]
Zhang, Peng [1 ,2 ]
Wang, Yue [1 ]
Qu, Jingping [1 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] Michigan State Univ, Dept Chem, E Lansing, MI 48824 USA
基金
中国国家自然科学基金;
关键词
Ruthenium catalyst; Carbon nanotube; Hydrogenation; Fine chemical; Benzene; p-Chloronitrobenzene; Cinnamaldehyde; Confinement effect; Electronic effect; Heat treating; ENHANCED CATALYTIC-ACTIVITY; SELECTIVE HYDROGENATION; PARTICLE-SIZE; ALPHA; BETA-UNSATURATED ALDEHYDES; REGIOSELECTIVE HYDROGENATION; ASYMMETRIC HYDROGENATION; PREFERENTIAL OXIDATION; UNSATURATED ALDEHYDES; BENZENE HYDROGENATION; BIMETALLIC CATALYSTS;
D O I
10.1016/j.jcat.2015.04.034
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
For the purpose as stated in title, three Ru catalysts were prepared with the same treated carbon nanotubes. One has most of Ru nanoparticles confined inside the channels, and the other two have most of Ru nanoparticles outside through different preparation methods. Heat treating was performed to obtain another three catalysts. Characterization by X-ray photoelectron spectroscopy indicated that heat treating made Ru nanoparticles electron rich. Hydrogenation of benzene, p-chloronitrobenzene, and cinnamaldehyde was chosen as model reactions to evaluate all these catalysts. Electronic effect plays an important role in catalytic performance. The electron-rich Ru would be favorable for p-chloronitrobenzene hydrogenation, but unfavorable for benzene hydrogenation. For cinnamaldehyde hydrogenation, the electron-rich Ru would be favorable for adsorption of C=O bond rather than C=C bond and thus promoted the selectivity to cinnamyl alcohol. A confinement effect induced by the electronic effect has different influences on these substrates, and it can be enhanced by heat treating for all the reactions. Finally, we drew a correlation of electronic structures between catalysts and substrates accounting for these phenomena. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:95 / 106
页数:12
相关论文
共 65 条
[1]   Iron catalysts supported on carbon nanotubes for Fischer-Tropsch synthesis: Effect of catalytic site position [J].
Abbaslou, Reza M. Malek ;
Tavassoli, Ahmad ;
Soltan, Jafar ;
Dalai, Ajay K. .
APPLIED CATALYSIS A-GENERAL, 2009, 367 (1-2) :47-52
[2]   Work functions and surface functional groups of multiwall carbon nanotubes [J].
Ago, H ;
Kugler, T ;
Cacialli, F ;
Salaneck, WR ;
Shaffer, MSP ;
Windle, AH ;
Friend, RH .
JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (38) :8116-8121
[3]   An Efficient Strategy to Drive Nanoparticles into Carbon Nanotubes and the Remarkable Effect of Confinement on Their Catalytic Performance [J].
Castillejos, Eva ;
Debouttiere, Pierre-Jean ;
Roiban, Lucian ;
Solhy, Abderrahim ;
Martinez, Victor ;
Kihn, Yolande ;
Ersen, Ovidiu ;
Philippot, Karine ;
Chaudret, Bruno ;
Serp, Philippe .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (14) :2529-2533
[4]   Effect of confinement in carbon nanotubes on the activity of Fischer-Tropsch iron catalyst [J].
Chen, Wei ;
Fan, Zhongli ;
Pan, Xiulian ;
Bao, Xinhe .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (29) :9414-9419
[5]   Enhancement of the Performance of a Platinum Nanocatalyst Confined within Carbon Nanotubes for Asymmetric Hydrogenation [J].
Chen, Zhijian ;
Guan, Zaihong ;
Li, Mingrun ;
Yang, Qihua ;
Li, Can .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (21) :4913-4917
[6]   Structure-activity relationships in catalysis by metals: some aspects of particle size, bimetallic and supports effects [J].
Coq, B ;
Figueras, F .
COORDINATION CHEMISTRY REVIEWS, 1998, 178 :1753-1783
[7]   LIQUID-PHASE HYDROGENATION OF CINNAMALDEHYDE OVER SUPPORTED RUTHENIUM CATALYSTS - INFLUENCE OF PARTICLE-SIZE, BIMETALLICS AND NATURE OF SUPPORT [J].
COQ, B ;
KUMBHAR, PS ;
MOREAU, C ;
MOREAU, P ;
WARAWDEKAR, MG .
JOURNAL OF MOLECULAR CATALYSIS, 1993, 85 (02) :215-228
[8]   COMPETITIVE C=C AND C=O ADSORPTION OF ALPHA-BETA-UNSATURATED ALDEHYDES ON PT AND PD SURFACES IN RELATION WITH THE SELECTIVITY OF HYDROGENATION REACTIONS - A THEORETICAL APPROACH [J].
DELBECQ, F ;
SAUTET, P .
JOURNAL OF CATALYSIS, 1995, 152 (02) :217-236
[9]   Chemoselective hydrogenation of α,β-unsaturated aldehydes with modified Pd/C catalyst [J].
Du, Wen Qiang ;
Rong, Ze Ming ;
Liang, Yan ;
Wang, Yong ;
Lu, Xin Yi ;
Wang, Yi Fan ;
Lu, Lian Hai .
CHINESE CHEMICAL LETTERS, 2012, 23 (07) :773-776
[10]  
Du WQ, 2012, CHEM RES CHINESE U, V28, P882