Direct synthesis of Pd incorporated in mesoporous silica for solvent-free selective hydrogenation of chloronitrobenzenes

被引:26
|
作者
Yu, Wen [1 ]
Lin, Hsin-Wei [1 ]
Tan, Chung-Sung [1 ]
机构
[1] Natl Tsing Hua Univ, Dept Chem Engn, Hsinchu 30013, Taiwan
关键词
Direct synthesis; Pd-MS; 1; 3; 5-Trimethylbenzene; Solvent-free hydrogenation; Chloronitrobenzene; SUPERCRITICAL CARBON-DIOXIDE; O-CHLORONITROBENZENE; PALLADIUM NANOPARTICLES; COUPLING REACTIONS; HETEROGENEOUS CATALYST; HIGHLY EFFICIENT; CO OXIDATION; CHLOROANILINE; DEPOSITION; SUPPORT;
D O I
10.1016/j.cej.2017.05.051
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Pd incorporated in mesoporous silica (Pd-MS) catalysts were prepared by a direct synthesis method in the presence of 1, 3, 5-trimethylbenzene (TMB) and their formation mechanism was proposed. TMB not only acted as an effective expanding agent to enlarge pore size and pore volume of MS but also acted as a structure-directing agent to induce the formation of worm-like morphology. For solvent-free hydrogenation of p-chloronitrobenzene (p-CNB), a complete conversion of p-CNB with a selectivity towards p-chloroaniline of 99.9% over the Pd-MS catalyst with addition of TMB (Pd-MS-50-TMB, where 50 represented the addition of 5 mL of aqueous NH3) was obtained at 85 degrees C and 3.45 MPa of H-2 in 2 h, while only 48.4% p-CNB conversion over Pd-MS-50 synthesized without TMB was obtained. The enhanced activity of the Pd-MS-50-TMB was not only attributed to the smaller size of Pd particles, but also to the worm-like morphology of the support with larger pore size and pore volume that could enhance mass transfer and allow the reactants more facile access to Pd for reaction. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:124 / 133
页数:10
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