A highly active non-precious metal catalyst based on Fe-N-C@CNTs for nitroarene reduction

被引:9
|
作者
Chen, Jian [1 ,2 ]
Yao, Yi [1 ,2 ]
Zhao, Jiao [1 ]
Zhao, Yaopeng [1 ]
Zheng, Yuanyuan [1 ]
Li, Mingrun [1 ]
Yang, Qihua [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
来源
RSC ADVANCES | 2016年 / 6卷 / 98期
关键词
MOLECULARLY DEFINED COMPLEXES; CARBON NANOTUBES; HYDROGEN STORAGE; IRON; SITES; SPILLOVER; 4-NITROPHENOL; NANOPARTICLES; ENHANCEMENT; TEMPERATURE;
D O I
10.1039/c6ra20666b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Research on transition metal-nitrogen-carbon (M-N-C) materials revealed their potential as catalysts in several important traditional reactions. However, the activity of M-N-C still needs to be further improved and the real active center of M-N-C catalysts is still under debate. In this work, an efficient Fe-N-C@CNTs for the hydrogenation of nitroarenes was prepared by pyrolysis of FeCl3, phenanthroline and CNTs. Fe-N-C supported on CNTs is much more active than that supported on activated carbon, showing the promotion effect of CNTs. The characterization results suggest that the high activity of Fe-N-C is mainly attributed to the formation of epsilon-Fe3N, which is the active site for the hydrogenation reaction. Nitrogen/carbon atoms contacted to the active centers could serve as bridges to transport the dissociated hydrogen atoms via spillover effect. The catalytic performance of Fe-N-C was also tested on fixed bed reactor under continuous flow condition for the first time and could smoothly catalyze the reaction for over 300 hours.
引用
收藏
页码:96203 / 96209
页数:7
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