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

被引:106
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
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
相关论文
共 43 条
[1]  
[Anonymous], 1995, Handbook of X-ray Photoelectron Spectroscopy. A Reference Book of Standard Spectra for Identification and Interpretation of XPS Data
[2]   High efficiency steam reforming of ethanol by cobalt-based catalysts [J].
Batista, MS ;
Santos, RKS ;
Assaf, EM ;
Assaf, JM ;
Ticianelli, EA .
JOURNAL OF POWER SOURCES, 2004, 134 (01) :27-32
[3]   Characterization of the activity and stability of supported cobalt catalysts for the steam reforming of ethanol [J].
Batista, MS ;
Santos, RKS ;
Assaf, EM ;
Assaf, JM ;
Ticianelli, EA .
JOURNAL OF POWER SOURCES, 2003, 124 (01) :99-103
[4]   Effect of pretreatment on the activity of a Ru-promoted Co/Al2O3 Fischer-Tropsch catalyst [J].
Belambe, AR ;
Oukaci, R ;
Goodwin, JG .
JOURNAL OF CATALYSIS, 1997, 166 (01) :8-15
[5]   Novel zirconia-supported catalysts for low-temperature oxidative steam reforming of ethanol [J].
Bi, Jia-Lin ;
Hong, Yeh-Yeau ;
Lee, Chia-Chan ;
Yeh, Chuin-Tih ;
Wang, Chen-Bin .
CATALYSIS TODAY, 2007, 129 (3-4) :322-329
[6]   Metal-catalysed steam reforming of ethanol in the production of hydrogen for fuel cell applications [J].
Breen, JP ;
Burch, R ;
Coleman, HM .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2002, 39 (01) :65-74
[7]   Hydrogen produced from ethanol for internal reforming molten carbonate fuel cell [J].
Cavallaro, S ;
Mondello, N ;
Freni, S .
JOURNAL OF POWER SOURCES, 2001, 102 (1-2) :198-204
[8]   Molecular beam epitaxial growth and properties of CoFe2O4 on MgO(001) [J].
Chambers, SA ;
Farrow, RFC ;
Maat, S ;
Toney, MF ;
Folks, L ;
Catalano, JG ;
Trainor, TP ;
Brown, GE .
JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS, 2002, 246 (1-2) :124-139
[9]   X-RAY PHOTOELECTRON-SPECTROSCOPY STUDY OF THE SURFACE-COMPOSITION OF COO-MGO SOLID-SOLUTIONS [J].
CIMINO, A ;
DEANGELIS, BA ;
MINELLI, G .
SURFACE AND INTERFACE ANALYSIS, 1983, 5 (04) :150-154