Cobalt Nanoparticles Encapsulated in Nitrogen-Doped Carbon Shells: Efficient and Stable Catalyst for Nitrobenzene Reduction

被引:60
|
作者
Xu, Yan [2 ]
Shan, Weixiang [2 ]
Liang, Xiang [2 ]
Gao, Xiaohui [1 ]
Li, Wenzhang [2 ]
Li, Hongmei [1 ]
Qiu, Xiaoqing [2 ]
机构
[1] Cent South Univ, Sch Phys Sci & Elect, Changsha 41083, Peoples R China
[2] Cent South Univ, Coll Chem & Chem Engn, Changsha 41083, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORK; IN-SITU SYNTHESIS; POROUS CARBON; BIFUNCTIONAL ELECTROCATALYSTS; CO NANOPARTICLES; HYDROGENATION; NANOTUBES; 4-NITROPHENOL; PERFORMANCE; STORAGE;
D O I
10.1021/acs.iecr.9b06604
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In this work, cobalt nanoparticles@N-doped carbon nanocomposites (Co@NC) with controllable Co contents have been prepared by pyrolysis of Zn/Co bimetal zeolitic imidazolate framework-9 (Zn/Co-ZIF-9). The magnetic cobalt nanoparticles encapsulated by multilayered carbon shells are uniformly distributed on the NC substrates. The as-obtained Co@NC 45.8 wt % samples exhibit higher catalytic activity and stability for the heterogeneous catalytic reduction of nitrobenzene to anilines by NaBH4 under gentle condition. The reduction reaction over cog NC 45.8 wt % catalysts accords with pseudo-first-order kinetics with an apparent rate constant of 0.844 min(-1) and apparent activation energy of 14.20 kJ/mol at room temperature. Additionally, the related catalytic mechanism and reaction path have been fully explored and it has been found that the active hydrogen species induced by metallic cobalt nanoparticles, instead of the self-hydrolysis of NaBH4, accounts for the efficient reduction of nitrobenzene. Moreover, the Co@NC catalysts are greatly expedient for the separation and recycling from the reaction system due to its ferromagnetism, suggesting the promising application in the catalytic reduction reaction of nitrobenzene into anilines.
引用
收藏
页码:4367 / 4376
页数:10
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