In-situ synthesis of Ni-Mo2C/Al2O3 catalysts for dry reforming of methane

被引:25
作者
Duan, Yiping [1 ]
Shang, Ruishu [1 ]
Zhong, Xinyan [1 ]
Xie, Wei [1 ]
Wang, Xingyue [1 ]
Huang, Lihong [1 ,2 ,3 ]
机构
[1] Chengdu Univ Technol, Dept Chem & Pharmaceut Engn, Chengdu 610059, Peoples R China
[2] Indiana Univ Purdue Univ, Richard G Lugar Ctr Renewable Energy, Indianapolis, IN 46224 USA
[3] Indiana Univ Purdue Univ, Lugar Ctr Renewable Energy, 799 W Michigan St, Indianapolis, IN 46202 USA
基金
中国国家自然科学基金;
关键词
Dry reforming of methane; Hydrogen and syngas production; In-situ synthesis of Ni-Mo2C/Al2O3 catalyst; MOLYBDENUM CARBIDE CATALYSTS; ONE-POT SYNTHESIS; SYNTHESIS GAS; NIMO-AL2O3; CATALYSTS; COMBUSTION SYNTHESIS; ALUMINA; HYDRODESULFURIZATION; PERFORMANCE; STABILITY; HYDROGEN;
D O I
10.1016/j.ijhydene.2016.10.006
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
Dry reforming of methane (DRM) is considered a promising process to convert two major greenhouse gases (CH4 and CO2) into hydrogen and synthesis gas for chemical and fuel production. In the current work, NiMo Al2O3 samples were prepared by combustion synthesis via one-pot process using urea and starch as fuel, and then treated in a flow of CH4/CO2 at 800 degrees C to in-situ synthesize the Ni-Mo2C/Al2O3 catalyst, which was then tested in CH4/CO2 for DRM. The results indicate that the Ni-Mo2C/Al2O3 catalyst was successfully formed, and there was a strong interaction of Ni-0-Mo2C via in-situ carburization; within DRM, CH4 can be converted by Ni-0 into intermediate species of C*, and was then further transformed into CO by the adjacent Mo2C species in a catalytic cycle. Meanwhile, there were improved specific surface area and resistance to oxidation and sintering, as suggested by BET, XRD and XPS. As a result, the conversion of CO2 and mole ratio of H-2/CO maintained stable near 94% and 0.99, respectively, and the conversion of CH4 remained stable near 89.4% in a 15-h DRM test. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:21955 / 21964
页数:10
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