Sulfur-doped porous carbon supported palladium catalyst for high selective o-chloro-nitrobenzene hydrogenation

被引:22
|
作者
Zhang, Qunfeng [1 ]
Li, Kang [1 ]
Xiang, Yizhi [2 ]
Zhou, Yuan [1 ]
Wang, Qingtao [1 ]
Guo, Lingling [1 ]
Ma, Lei [1 ]
Xu, Xiaoliang [1 ]
Lu, Chunshan [1 ]
Feng, Feng [1 ]
Lv, Jinhui [1 ]
Ni, Jun [1 ]
Li, Xiaonian [1 ]
机构
[1] Zhejiang Univ Technol, Ind Catalysis Inst, State Key Lab Breeding Base Green Chem Synth Tech, Hangzhou 310032, Zhejiang, Peoples R China
[2] Mississippi State Univ, Dave C Swalm Sch Chem Engn, Mississippi State, MS 39762 USA
基金
中国国家自然科学基金;
关键词
Sulfur-modified carbon support; Selective hydrogenation; o-chloro-nitrobenzene; o-chloro-aniline; P-CHLORONITROBENZENE; DIPHENYL-SULFIDE; PD/C CATALYST; RUTHENIUM; ADSORPTION;
D O I
10.1016/j.apcata.2019.05.016
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
Sulfur-modified carbon support can effectively modulate the performance of the metal catalyst. Here we prepared a sulfur-doped mesoporous carbon material (CSx) through carbonization of poly(sodium p-styrenesulfonate or p-styrenesulfonate co-maleate), which was supported with Pd and employed for the selective hydrogenation of o-chloro-nitrobenzene (o-CNB) to o-chloro-aniline (o-CAN). Such catalyst shows almost 100% selectivity of o-CAN at 100% o-CNB conversion (performed In a batch reactor: t = 210 min, No-CNB/m(cat) = 0.63 mol/g(cat)). The stability (recyclability) study of the optimal catalyst shows that the catalyst can be reused for at least six times without decreasing the selectivity (100% conversion can be achieved with slightly prolonged reaction time). We suggest that the electronic effect between the S and Pd, which reduces the hydrogen adsorption and dissociation ability of Pd, to be responsible for the excellent selectivity, and the formation of C-S covalent bond to be responsible for the good stability.
引用
收藏
页码:74 / 81
页数:8
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