Enhanced catalytic performances of Ni/Al2O3 catalyst via addition of V2O3 for CO methanation

被引:112
作者
Liu, Qing [1 ]
Gu, Fangna [1 ]
Lu, Xiaopeng [1 ]
Liu, Youjun [1 ]
Li, Huifang [1 ]
Zhong, Ziyi [2 ]
Xu, Guangwen [1 ]
Su, Fabing [1 ]
机构
[1] Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, Beijing 100190, Peoples R China
[2] ASTAR, Inst Chem Engn & Sci, Jurong Island 627833, Singapore
基金
中国国家自然科学基金;
关键词
Ni/Al2O3; catalyst; Vanadium oxide; Ni3V2O8; CO methanation; CO2; methanation; SYNTHETIC NATURAL-GAS; PROMOTED RHODIUM CATALYSTS; CARBON-DIOXIDE; OXIDATIVE DEHYDROGENATION; NI/TIO2; CATALYST; OVEN GAS; HYDROGENATION; VANADIUM; SYNGAS; TEMPERATURE;
D O I
10.1016/j.apcata.2014.09.028
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
Highly active and coking resistant Ni-V2O3/Al2O3 catalysts were prepared by co-impregnation method for CO and CO2 methanation. The influence of vanadium oxide addition on catalyst structure, distribution and reducibility of Ni species, morphology and surface characteristics, was investigated in detail. Compared to the catalyst without vanadium, the Ni-V2O3/Al2O3 catalysts showed significant improvement in the activity, thermal stability, and resistance to coke formation in CO methanation. In addition, these catalysts also showed high activities for CO2 methanation at both atmospheric and 2.0 MPa pressures. It was found that Ni3V2O8 was formed during the calcination of the Ni-V2O3/Al2O3 catalysts, which led to the formation of smaller Ni particle sizes (ca. 3.0 nm) as compared to the case without vanadium oxide addition. The higher catalytic activity over the Ni-V2O3/Al2O3 catalysts for CO methanation was mainly due to the larger H-2 uptake, the higher Ni dispersion as well as the smaller metallic Ni nanoparticles. The oxidation-reduction cycle of V2O3 could increase the oxygen vacancies, which enhanced the dissociation of CO2 by-product and generated surface oxygen intermediates, thus preventing carbon deposition on the Ni particles in CO methanation. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:37 / 47
页数:11
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