Ni/Mg-Al mixed oxide catalyst for the steam reforming of ethanol

被引:126
作者
Coleman, L. J. I. [1 ]
Epling, W. [1 ]
Hudgins, R. R. [1 ]
Croiset, E. [1 ]
机构
[1] Univ Waterloo, Dept Chem Engn, Waterloo, ON N2L 3G1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Ethanol steam reforming; Hydrogen production; Nickel; Hydrotalcite; Mixed oxide support; NI-BASED CATALYSTS; MC FUEL-CELL; LAYERED DOUBLE HYDROXIDES; ACID-BASE PROPERTIES; HYDROGEN-PRODUCTION; BIO-ETHANOL; THERMODYNAMIC ANALYSIS; PARTIAL OXIDATION; NICKEL-CATALYSTS; LOW-TEMPERATURE;
D O I
10.1016/j.apcata.2009.04.032
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 10 wt% Ni-loaded Mg-Al mixed oxide supported catalysts were evaluated for the production of hydrogen via the steam reforming of ethanol. Mg-Al mixed oxide supported nickel catalysts were found to give superior activity, H-2 and COx product selectivity, and improved catalyst stability compared to the pure oxide supported nickel catalysts. Performance was dependent upon the A and Mg content of the support. At 923 K, the mixed oxide supported catalysts exhibited the highest H-2 and COx yields and were stable, showing no signs of deactivation after 20 h of operation. The improved performance of these catalysts was related to the incorporation of the pure oxides, MgO and Al2O3, into a MgAl2O4 phase. The formation of MgAl2O4 reduced nickel incorporation into the supports leaving nickel in its active form. In addition, the formation of MgAl2O4, a slightly basic material, exhibited moderate acidic and basic site strength and density compared to the pure oxide supported catalysts. Moderation of the acid-base properties improved the activity, selectivity, and stability of the catalysts by reducing activity for by-product reactions. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:52 / 63
页数:12
相关论文
共 58 条
[1]   Preparation and characterization of MgO/Al2O3 mixed oxides support for hydrotreating catalysts [J].
Aberuagba, F ;
Kumar, M ;
Gupta, JK ;
Muralidhar, G ;
Sharma, LD .
REACTION KINETICS AND CATALYSIS LETTERS, 2002, 75 (02) :245-250
[2]   MAGNESIA-SUPPORTED NICKEL-CATALYSTS .1. FACTORS AFFECTING THE STRUCTURE AND MORPHOLOGICAL PROPERTIES [J].
ARENA, F ;
HORRELL, BA ;
COCKE, DL ;
PARMALIANA, A ;
GIORDANO, N .
JOURNAL OF CATALYSIS, 1991, 132 (01) :58-67
[3]   Hydrogen production for fuel cells from the catalytic ethanol steam reforming [J].
Aupretre, F ;
Descorme, C ;
Duprez, D .
TOPICS IN CATALYSIS, 2004, 30-1 (1-4) :487-491
[4]   Ethanol steam reforming over MgxNi1-xAl2O3 spinel oxide-supported Rh catalysts [J].
Aupretre, F ;
Descorme, C ;
Duprez, D ;
Casanave, D ;
Uzio, D .
JOURNAL OF CATALYSIS, 2005, 233 (02) :464-477
[5]   Mechanisms of catalyst deactivation [J].
Bartholomew, CH .
APPLIED CATALYSIS A-GENERAL, 2001, 212 (1-2) :17-60
[6]   Preparation and characterisation of a stable Rh catalyst for the partial oxidation of methane [J].
Basile, F ;
Fornasari, G ;
Gazzano, M ;
Kiennemann, A ;
Vaccari, A .
JOURNAL OF CATALYSIS, 2003, 217 (02) :245-252
[7]   Catalytic partial oxidation and CO2-reforming on Rh- and Ni-based catalysts obtained from hydrotalcite-type precursors [J].
Basile, F ;
Fornasari, G ;
Poluzzi, E ;
Vaccari, A .
APPLIED CLAY SCIENCE, 1998, 13 (5-6) :329-345
[8]   Bio-ethanol steam reforming: Insights on the mechanism for hydrogen production [J].
Benito, M ;
Sanz, JL ;
Isabel, R ;
Padilla, R ;
Arjona, R ;
Daza, L .
JOURNAL OF POWER SOURCES, 2005, 151 :11-17
[9]   Effect of calcination temperature on catalyst reducibility and hydrogenation reactivity in rice husk ash-alumina supported nickel systems [J].
Chang, FW ;
Kuo, MS ;
Tsay, MT ;
Hsieh, MC .
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2004, 79 (07) :691-699
[10]   Gas chromatography method for the characterization of ethanol steam reforming products [J].
Chladek, Petr ;
Coleman, Luke J. I. ;
Croiset, E. ;
Hudgins, Robert R. .
JOURNAL OF CHROMATOGRAPHIC SCIENCE, 2007, 45 (03) :153-157