Immobilization of highly active Pd nano-catalysts on functionalized mesoporous silica supports using mercapto groups as anchoring sites and their catalytic performance for phenol hydrogenation

被引:15
|
作者
Zhang, Jiaxi [1 ]
Huang, Gaowei [1 ]
Zhang, Cheng [1 ,2 ]
He, Qunhua [2 ]
Huang, Chao [1 ]
Yang, Xu [3 ]
Song, Huiyu [1 ]
Liang, Zhenxing [1 ]
Du, Li [1 ,4 ]
Liao, Shijun [1 ,4 ]
机构
[1] S China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510640, Guangdong, Peoples R China
[2] Guangdong Environm Monitoring Ctr, Guangzhou 510640, Guangdong, Peoples R China
[3] Chinese Acad Sci, Key Lab Renewable Energy & Gas Hydrate, Guangzhou Inst Energy Convers, Guangzhou 510640, Guangdong, Peoples R China
[4] S China Univ Technol, Sch Chem & Chem Engn, Key Lab Fuel Cell Technol Guangdong Prov, Guangzhou 510640, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Mesoporous silica; Mercapto group functionalization; Palladium; Anchoring; Supported catalyst; Phenol hydrogenation; CYCLOHEXANONE; NANOSPHERES; ADSORPTION; LIPASE; SBA-15;
D O I
10.1016/S1872-2067(12)60603-2
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Highly active and highly dispersed Pd-loaded nano-catalysts using mercapto group (-SH) functionalized mesoporous silica supports, namely, Pd-SH-MCM-41 and Pd-SH-SBA-15, were prepared using an impregnation-reduction approach. The surface -SH groups are believed to facilitate the high distribution and immobilization of the Pd nanoparticles within the silica supports through an anchoring interaction. The catalysts featured long-range ordered structures, uniform pore size, high surface area, and highly dispersed Pd nanoparticles as characterized by X-ray diffraction, N-2 adsorption-desorption, and transmission electron microscopy. The catalysts showed activity five times higher than that of commercial Pd/C catalyst and three times higher than those of Pd/MCM-41 and Pd/SBA-15 catalysts. Within 1 h of reaction at 80 degrees C and 1.0 MPa, the conversion of phenol attained was greater than 99%, and the selectivity for cyclohexanone was 98%. (C) 2013, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1519 / 1526
页数:8
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