Efficient Co/NSPC catalyst for selective hydrogenation of halonitrobenzenes and mechanistic insight

被引:3
|
作者
Xu, Jiahui [1 ]
Chen, Xianlang [2 ]
Bai, Jia-qi [1 ,3 ]
Miao, Zhengan [3 ]
Tan, Yuan [4 ]
Zhan, Nannan [4 ]
Liu, Huangfei [1 ]
Ma, Mei [1 ]
Cai, Mengdie [1 ]
Cheng, Qin [1 ]
Sun, Song [1 ]
机构
[1] Anhui Univ, Sch Chem & Chem Engn, Hefei 230601, Anhui, Peoples R China
[2] Taizhou Univ, Engn Res Ctr Recycling & Comprehens Utilizat Pharm, Taizhou 318000, Zhejiang, Peoples R China
[3] Sennics Co Ltd Anhui, 1111 West Cuihuliu Rd,Circulat Econ Ind Pk, Tongling 244000, Peoples R China
[4] Zhejiang Normal Univ, Hangzhou Inst Adv Studies, 1108 Gengwen Rd, Hangzhou 311231, Peoples R China
基金
中国国家自然科学基金; 安徽省自然科学基金;
关键词
DOPED CARBON HYBRIDS; CHEMOSELECTIVE HYDROGENATION; P-CHLORONITROBENZENE; MESOPOROUS SILICA; ACTIVATED CARBON; HIGH-PERFORMANCE; CO; COBALT; NANOPARTICLES; NITROARENES;
D O I
10.1039/d3cy01767b
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
The selective hydrogenation of halonitrobenzenes (HNBs) to haloanilines (HANs) is an efficient method to prepare key intermediates in the fine chemical industry. It is still a challenge to develop non-noble metal-based heterogeneous hydrogenation catalysts to achieve high activity and selectivity for this reaction. Herein, we reported a N, S co-doped mesoporous carbon supported Co catalyst for hydrogenation of HNBs, the prepared 5%Co/NSPC-800 catalyst showed superior catalytic performance with a TOFs of 203 h(-1) and >99.9% selectivity to p-chloroaniline (p-CAN), and it also exhibited wide substrate applicability and can be reused at least 4 times. Furthermore, the reaction mechanism of p-CNB hydrogenation over 5%Co/NSPC-800 was proposed on the basis of kinetic studies, spectroscopic studies, and DFT calculations. The hydrogenation of p-CNB over 5%Co/NSPC-800 followed the condensation route, and Co-0 and Co-N-x were the main active sites for this reaction.
引用
收藏
页码:1167 / 1180
页数:14
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