Influence of the metal sites of M-N-C (M = Co, Fe, Mn) catalysts derived from metalloporphyrins in ethylbenzene oxidation

被引:35
作者
Fu, Lingling [1 ]
Lu, Yijuan [1 ]
Liu, Zhigang [1 ]
Zhu, Runliang [2 ]
机构
[1] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemobiosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
[2] Chinese Acad Sci, Guangzhou Inst Geochem, Guangzhou 510640, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
M; (cobalt; iron; manganese)-N-C; Transition metal; Nitrogen-doped carbon; Porphyrin; Ethylbenzene oxidation; NITROGEN-DOPED CARBON; OXYGEN REDUCTION REACTION; ONE-POT METHOD; SELECTIVE OXIDATION; ELECTROCATALYSTS; NANOPARTICLES; PERFORMANCE; HYDROGEN; NANOCOMPOSITE; NANOTUBES;
D O I
10.1016/S1872-2067(15)61029-4
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Transition metal catalysts M-N-C (M = Co, Fe, Mn) were synthesized by a template-free method by heating meso-tetraphenyl porphyrins (i.e. CoTPP, FeTPPCI, MnTPPCl) precursors. The catalysts were characterized by N-2 adsorption-desorption, thermogravimetry, high-resolution transmission electron microscopy, and Raman and X-ray photoelectron spectroscopy. The selective oxidation of ethylbenzene with molecular oxygen under a solvent-free condition was carried out to explore the catalytic performance of the M-N-Cs, which exhibited different catalytic performance. That was ascribed to the difference in M (Co, Fe, Mn) and different graphitization degree forming during the heating process, in which M (Co, Fe, Mn) might have different catalytic activity on the formation of the M-N-C catalyst. All the M-N-C composites had remarkable recyclability in the selective oxidation of ethylbenzene. (C) 2016, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:398 / 404
页数:7
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