Nickel catalysts for internal reforming in molten carbonate fuel cells

被引:38
作者
Berger, RJ
Doesburg, EBM
vanOmmen, JG
Ross, JRH
机构
[1] UNIV TWENTE,FAC CHEM TECHNOL,LAB INORGAN CHEM MAT SCI & CATALYSIS,NL-7500 AE ENSCHEDE,NETHERLANDS
[2] UNIV LIMERICK,DEPT CHEM & ENVIRONM SCI,LIMERICK,IRELAND
关键词
molten carbonate fuel cell; nickel; steam reforming; lithium; potassium; deactivation;
D O I
10.1016/0926-860X(96)00099-3
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
Natural gas may be used instead of hydrogen as fuel for the molten carbonate fuel cell (MCFC) by steam reforming the natural gas inside the MCFC, using a nickel catalyst (internal reforming). The severe conditions inside the MCFC, however, require that the catalyst has a very high stability. In order to find suitable types of nickel catalysts and to obtain more knowledge about the deactivation mechanism(s) occurring during internal reforming, a series of nickel catalysts was prepared and subjected to stability tests at 973 K in an atmosphere containing steam and lithium and potassium hydroxide vapours. All the catalysts prepared showed a significant growth of the nickel crystallites during the test, especially one based on alpha-Al2O3 and a coprecipitated Ni/Al2O3 sample having a very high nickel content. However, this growth of nickel crystallites only partially explained the very strong deactivation observed in most cases. Only a coprecipitated nickel/alumina catalyst with high alumina content and a deposition-precipitation catalyst showed satisfactory residual activities. Addition of magnesium or lanthanum oxide to a coprecipitated nickel/alumina catalyst decreased the stability. Adsorption and retention of the alkali was the most important factor determining the stability of a catalyst in an atmosphere containing alkali hydroxides. This is because the catalyst bed may remain active if a small part of the catalyst bed retains all the alkali.
引用
收藏
页码:343 / 365
页数:23
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