Synthesis gas production in the combined CO2 reforming with partial oxidation of methane over Ce-promoted Ni/SiO2 catalysts

被引:88
|
作者
Li, Baitao [1 ]
Xu, Xiujuan [1 ]
Zhang, Shuyi [1 ]
机构
[1] S China Univ Technol, Dept Chem & Chem Engn, Key Lab Fuel Cell Technol Guangdong Prov, Guangzhou 510640, Peoples R China
基金
中国国家自然科学基金;
关键词
Methane reforming; Nickel-cerium-silica catalyst; Syngas; Hydrogen production; Ni/SiO2; CARBON-DIOXIDE; NICKEL-CATALYSTS; NI CATALYSTS; SYNGAS; CERIA; HYDROGEN; SURFACE; MGO; RH; MICROSTRUCTURE;
D O I
10.1016/j.ijhydene.2012.10.103
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
A series of nickel-based catalyst supported on silica (Ni/SiO2) with different loading of Ce/Ni (molar ratio ranging from 0.17 to 0.84) were prepared using conventional co-impregnation method and were applied to synthesis gas production in the combination of CO2 reforming with partial oxidation of methane. Among the cerium-containing catalysts, the cerium-rich ones exhibited the higher activity and stability than the cerium-low ones. The temperature-programmed reduction (TPR) and UV-vis diffuse reflectance spectroscopy (UV-vis DRS) analysis revealed that the addition of CeO2 reduced the chemical interaction between Ni and support, resulting in an increase in reducibility and dispersion of Ni. Over NiCe-x/SiO2 (x = 0.17, 0.50, 0.67, 0.84) catalysts, the reduction peak in TPR profiles shifted to the higher temperature with increasing Ce/Ni molar ratio, which was attributed to the smaller metallic nickel size of the reduced catalysts. The transmission electron microscopy (TEM) and X-ray diffraction (XRD) for the post-reaction catalysts confirmed that the promoter retained the metallic nickel species and prevented the metal particle growth at high reaction temperature. The NiCe-0.84/SiO2 catalyst with small Ni particle size exhibited the stable activity with the constant H-2/CO molar ratio of 1.2 during 6-h reaction in the combination of CO2 reforming with partial oxidation of methane at 850 degrees C and atmospheric pressure. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:890 / 900
页数:11
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