催化作用
煅烧
蒸汽重整
X射线光电子能谱
化学
选择性
无机化学
水煤气变换反应
多相催化
程序升温还原
化学工程
有机化学
制氢
工程类
作者
Ayman M. Karim,Yu Su,Mark Engelhard,David L. King,Yong Wang
摘要
The catalytic roles of Co0 and Co2+ during steam reforming of ethanol were investigated over Co/MgO catalysts. Catalysts with different Co0/(Co0+Co2+) fraction were prepared through calcination and/or reduction at different temperatures, and the Co0 fraction was quantified by temperature programmed reduction (TPR) and in situ X-ray photoelectron spectroscopy (XPS). Higher temperature calcination of Co/MgO allowed us to prepare catalysts with more nonreducible Co2+ incorporated in the MgO lattice, while lower calcination temperatures allowed for the preparation of catalysts with higher Co0/(Co0+Co2+) fractions. The catalytic tests on Co0, nonreducible Co2+, and reducible Co2+ indicated that Co0 is much more active than either reducible or nonreducible Co2+ for C−C cleavage and water gas shift reaction. In addition, catalysts with a higher Co0 surface fraction exhibited a lower selectivity to CH4.
科研通智能强力驱动
Strongly Powered by AbleSci AI