催化作用
镍
甲烷
二氧化碳重整
碳纤维
二氧化碳
无机化学
热重分析
材料科学
化学
合成气
化学工程
冶金
有机化学
复合数
复合材料
工程类
作者
Shaobin Wang,Gao Qing Lu
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:1998-01-16
卷期号:12 (2): 248-256
被引量:93
摘要
Catalytic activities and deactivation characteristics of oxides-supported nickel catalysts for the reaction of methane reforming with carbon dioxide were investigated. The dynamic carbon deposition on various nickel catalysts was also studied by a thermogravimetric method. Among the catalysts prepared, Ni/La2O3, Ni/α-Al2O3, Ni/SiO2, and Ni/CeO2 showed very high CH4 and CO2 conversions and moderate deactivation whereas Ni/MgO and Ni/TiO2 had lower conversions when the Ni reduction was conducted at 500 °C. When Ni/MgO catalyst was reduced at 800 °C, it exhibited not only comparable conversions of CH4 and CO2 with other active catalysts but also much longer period of stability without deactivation. The amount of carbon deposited in Ni-based catalysts varied depending on the nature of support and followed the order of Ni/La2O3 > Ni/α-Al2O3 > Ni/SiO2 > Ni/MgO > Ni/CeO2 at 700 °C. The carbons formed on the catalyst surface showed different structural and chemical properties, and these in turn affected the catalytic activity of the catalysts.
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