Catalytic Roles of Co0 and Co2+ during Steam Reforming of Ethanol on Co/MgO Catalysts

被引:104
作者
Karim, Ayman M. [1 ]
Su, Yu [1 ]
Engelhard, Mark H. [2 ]
King, David L. [1 ]
Wang, Yong [1 ,3 ]
机构
[1] Pacific NW Natl Lab, Inst Interfacial Catalysis, Richland, WA 99354 USA
[2] Pacific NW Natl Lab, Environm Mol Sci Lab, Richland, WA 99354 USA
[3] Washington State Univ, Gene & Linda Voiland Sch Chem Engn & Bioengn, Pullman, WA 99164 USA
来源
ACS CATALYSIS | 2011年 / 1卷 / 04期
关键词
ethanol steam reforming; reaction pathway; Co-0; Co2+; XPS; cobalt oxidation state; SUPPORTED COBALT CATALYSTS; RAY PHOTOELECTRON-SPECTROSCOPY; FUEL-CELL APPLICATIONS; HYDROGEN-PRODUCTION; SOLID-SOLUTIONS; CU CATALYSTS; XPS ANALYSIS; OXIDE; TEMPERATURE; NI;
D O I
10.1021/cs200014j
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
The catalytic roles of Co-0 and Co2+ during steam reforming of ethanol Were investigated over Co/MgO catalysts. Catalysts with different Co-0/(Co-0 + Co2+) fraction were prepared through calcination and/or reduction at different temperatures, and the Co-0 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 tempratures allowed for the preparation of catalysts with higher Co-0/(Co-0 + Co2+) fractions. The catalytic tests on Co-0, nonreducible Co2+, and reducible Co2+ indicated that Co-0 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 Co-0 surface fraction exhibited a lower selectivity to CH4.
引用
收藏
页码:279 / 286
页数:8
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