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

被引:124
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
    Aberuagba, F
    Kumar, M
    Gupta, JK
    Muralidhar, G
    Sharma, LD
    [J]. REACTION KINETICS AND CATALYSIS LETTERS, 2002, 75 (02): : 245 - 250
  • [2] MAGNESIA-SUPPORTED NICKEL-CATALYSTS .1. FACTORS AFFECTING THE STRUCTURE AND MORPHOLOGICAL PROPERTIES
    ARENA, F
    HORRELL, BA
    COCKE, DL
    PARMALIANA, A
    GIORDANO, N
    [J]. JOURNAL OF CATALYSIS, 1991, 132 (01) : 58 - 67
  • [3] Hydrogen production for fuel cells from the catalytic ethanol steam reforming
    Aupretre, F
    Descorme, C
    Duprez, D
    [J]. TOPICS IN CATALYSIS, 2004, 30-1 (1-4) : 487 - 491
  • [4] Ethanol steam reforming over MgxNi1-xAl2O3 spinel oxide-supported Rh catalysts
    Aupretre, F
    Descorme, C
    Duprez, D
    Casanave, D
    Uzio, D
    [J]. JOURNAL OF CATALYSIS, 2005, 233 (02) : 464 - 477
  • [5] Mechanisms of catalyst deactivation
    Bartholomew, CH
    [J]. 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
    Basile, F
    Fornasari, G
    Gazzano, M
    Kiennemann, A
    Vaccari, A
    [J]. 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
    Basile, F
    Fornasari, G
    Poluzzi, E
    Vaccari, A
    [J]. APPLIED CLAY SCIENCE, 1998, 13 (5-6) : 329 - 345
  • [8] Bio-ethanol steam reforming: Insights on the mechanism for hydrogen production
    Benito, M
    Sanz, JL
    Isabel, R
    Padilla, R
    Arjona, R
    Daza, L
    [J]. 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
    Chang, FW
    Kuo, MS
    Tsay, MT
    Hsieh, MC
    [J]. JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2004, 79 (07) : 691 - 699
  • [10] Gas chromatography method for the characterization of ethanol steam reforming products
    Chladek, Petr
    Coleman, Luke J. I.
    Croiset, E.
    Hudgins, Robert R.
    [J]. JOURNAL OF CHROMATOGRAPHIC SCIENCE, 2007, 45 (03) : 153 - 157