Mesoporous nickel catalyst supported on multi-walled carbon nanotubes for carbon dioxide methanation

被引:110
|
作者
Wang, Wei [1 ,2 ,3 ]
Chu, Wei [1 ,2 ,3 ]
Wang, Ning [4 ]
Yang, Wen [1 ]
Jiang, Chengfa [1 ]
机构
[1] Sichuan Univ, Dept Chem Engn, Chengdu 610065, Sichuan, Peoples R China
[2] Sichuan Univ, Inst New Energy & Low Carbon Technol, Chengdu 610225, Sichuan, Peoples R China
[3] Sichuan Prov Engn Technol Ctr Environm Protect Ca, Chengdu 610064, Sichuan, Peoples R China
[4] Tsinghua Univ, Beijing Key Lab Green Chem React Engn & Technol, Dept Chem Engn, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Nickel-based catalyst; Carbon dioxide methanation; Confinement effect; Carbon nanotubes; Ultrasonic-assisted co-impregnation; Activation energy; CO2; METHANATION; NI/AL2O3; CATALYSTS; CONVERSION; REDUCTION; HYDROGEN; CAPTURE; ZRO2; CONFINEMENT; EMISSIONS; INSIGHT;
D O I
10.1016/j.ijhydene.2015.11.133
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
Nickel-based catalysts supported on multi-walled carbon nanotubes (CNTs) promoted with cerium were successfully synthesized by ultrasonic-assisted co-impregnation, using gamma-Al2O3 as comparative support, and employed in the carbon dioxide methanation reaction. Results indicated that the exceptional properties of CNTs together with the accession of cerium effectively enhanced the dispersion of metallic nickel, promoted the reduction of metal oxides and accelerated the CO2 activation. Meanwhile, the confinement effect of CNTs and the promotion effect of cerium could efficiently prevent the active species migration and sintering, and restricted the carbon deposition reaction. Catalytic performances exhibited that 12Ni4.5Ce/CNT catalyst possessed the highest activity with 83.8% conversion of CO2 and almost 100% selectivity of CH4 without obvious deactivation after 100 h stability test under reaction conditions. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:967 / 975
页数:9
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