SOFC system with integrated catalytic fuel processing

被引:37
作者
Finnerty, C [1 ]
Tompsett, GA [1 ]
Kendall, K [1 ]
Ormerod, RM [1 ]
机构
[1] Univ Keele, Birchall Ctr Inorgan Chem & Mat Sci, Keele ST5 5BG, Staffs, England
关键词
micro-SOFC; pre-reformer; combustion; catalyst; butane;
D O I
10.1016/S0378-7753(99)00496-6
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
In recent years, there has been much interest in the development of solid oxide fuel cell technology operating directly on hydrocarbon fuels. The development of a catalytic fuel processing system, which is integrated with the solid oxide fuel cell (SOFC) power source is outlined here. The catalytic device utilises a novel three-way catalytic system consisting of an in situ pre-reformer catalyst, the fuel cell anode catalyst and a platinum-based combustion catalyst. The three individual catalytic stages have been tested in a model catalytic microreactor. Both temperature-programmed and isothermal reaction techniques have been applied. Results from these experiments were used to design the demonstration SOFC unit. The apparatus used for catalytic characterisation can also perform in situ electrochemical measurements as described in previous papers [C.M. Finnerty, R.H. Cunningham, K. Kendall, R.M. Ormerod, Chem. Commun. (1998) 915-916; C.M. Finnerty, N.J. Coe, R.H. Cunningham, R.M. Ormerod, Catal. Today 46 (1998) 137-145]. This enabled the performance of the SOFC to be determined at a range of temperatures and reaction conditions, with current output of 290 mA cm(-2) at 0.5 V, being recorded. Methane and butane have been evaluated as fuels. Thus, optimisation of the in situ partial oxidation pre-reforming catalyst was essential, with catalysts producing high H-2/CO ratios at reaction temperatures between 873 K and 1173 K being chosen. These included Ru and Ni/Mo-based catalysts. Hydrocarbon fuels were directly injected into the catalytic SOFC system. Microreactor measurements revealed the reaction mechanisms as the fuel was transported through the three-catalyst device. The demonstration system showed that the fuel processing could be successfully integrated with the SOFC stack. (C) 2000 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:459 / 463
页数:5
相关论文
共 18 条
[1]  
Aparicio P. F., 1999, J CATAL, V184, P202
[2]   INFLUENCE OF MOLYBDENUM AND TUNGSTEN ADDITIVES ON THE PROPERTIES OF NICKEL STEAM REFORMING CATALYSTS [J].
BOROWIECKI, T ;
GOLEBIOWSKI, A .
CATALYSIS LETTERS, 1994, 25 (3-4) :309-313
[3]  
Boucouvalas J, 1997, STUD SURF SCI CATAL, V107, P435
[4]   Low NOx options in catalytic combustion and emission control [J].
Burch, R .
PURE AND APPLIED CHEMISTRY, 1996, 68 (02) :377-385
[5]   Some aspects of hydrocarbon activation on platinum group metal combustion catalysts [J].
Burch, R ;
Loader, PK ;
Urbano, FJ .
CATALYSIS TODAY, 1996, 27 (1-2) :243-248
[6]  
CUNNINGHAM RH, 1997, SOLID OXIDE FUEL CEL, V5, P965
[7]   Carbon formation on and deactivation of nickel-based/zirconia anodes in solid oxide fuel cells running on methane [J].
Finnerty, CM ;
Coe, NJ ;
Cunningham, RH ;
Ormerod, RM .
CATALYSIS TODAY, 1998, 46 (2-3) :137-145
[8]   A novel test system for in situ catalytic and electrochemical measurements on fuel processing anodes in working solid oxide fuel cells [J].
Finnerty, CM ;
Cunningham, RH ;
Kendall, K ;
Ormerod, RM .
CHEMICAL COMMUNICATIONS, 1998, (08) :915-916
[9]  
FINNERTY CM, 1999, PORT FUEL CELLS S LU
[10]  
KENDALL K, 1994, P 1 EUR SOL OX FUEL, P163