Diffusion and chemical reaction in the porous structures of solid oxide fuel cells

被引:26
作者
Haberman, B. A. [1 ]
Young, J. B. [1 ]
机构
[1] Univ Cambridge, Dept Engn, Hopkinson Lab, Cambridge CB2 1PZ, England
来源
JOURNAL OF FUEL CELL SCIENCE AND TECHNOLOGY | 2006年 / 3卷 / 03期
关键词
SOFC; CPIM; porous media; fuel cell simulations;
D O I
10.1115/1.2211637
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The Rolls-Royce integrated-planar solid oxide fuel cell (IP-SOFC) consists of ceramic modules with electrochemical cells printed on the outer surfaces. The cathodes are supplied with oxygen from air flowing over the outside of the module and the anodes are supplied with fuel diffusing from the internal gas channels. Natural gas is reformed into hydrogen in a separate reformer module of similar design except that the fuel cells are replaced by a reforming catalyst layer The performance of the modules is intrinsically linked to the behavior of the gas flows within their porous structures. The multicomponent convective-diffusive flows are simulated using a new theory of flow in porous material, the cylindrical pore. interpolation model. The effects of the catalyzed methane reforming and water-gas shift chemical reactions are also considered using appropriate kinetic models. It is found that the shift reaction, which is catalyzed by the anode material, has certain beneficial effects on the fuel cell module performance. The shift reaction enables the fuel cells to make effective use of carbon monoxide as a fuel when the supplied fuel has become depleted of hydrogen. In the reformer module the kinetics of the reaction make it difficult to sustain a high methane conversion rate. Although the analysis is based on IP-SOFC geometry, the modeling approach and general conclusions are applicable to other types of SOFCs.
引用
收藏
页码:312 / 321
页数:10
相关论文
共 22 条
[1]   Modeling of mass and heat transport in planar substrate type SOFCs [J].
Ackmann, T ;
de Haart, LGJ ;
Lehnert, W ;
Stolten, D .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2003, 150 (06) :A783-A789
[2]   Anode-supported intermediate temperature direct internal reforming solid oxide fuel cell. I: model-based steady-state performance [J].
Aguiar, P ;
Adjiman, CS ;
Brandon, NP .
JOURNAL OF POWER SOURCES, 2004, 138 (1-2) :120-136
[3]   High-temperature kinetics of the homogeneous reverse water-gas shift reaction [J].
Bustamante, F ;
Enick, RM ;
Cugini, AV ;
Killmeyer, RP ;
Howard, BH ;
Rothenberger, KS ;
Ciocco, MV ;
Morreale, BD .
AICHE JOURNAL, 2004, 50 (05) :1028-1041
[4]   Definition and sensitivity analysis of a finite volume SOFC model for a tubular cell geometry [J].
Campanari, S ;
Iora, P .
JOURNAL OF POWER SOURCES, 2004, 132 (1-2) :113-126
[5]   A complete polarization model of a solid oxide fuel cell and its sensitivity to the change of cell component thickness [J].
Chan, SH ;
Khor, KA ;
Xia, ZT .
JOURNAL OF POWER SOURCES, 2001, 93 (1-2) :130-140
[6]   Electrochemical model of the integrated planar solid oxide fuel cell (IP-SOFC) [J].
Costamagna, P ;
Selimovic, A ;
Del Borghi, M ;
Agnew, G .
CHEMICAL ENGINEERING JOURNAL, 2004, 102 (01) :61-69
[7]   INTERDIFFUSION OF GASES IN A LOW PERMEABILITY GRAPHITE AT UNIFORM PRESSURE [J].
EVANS, RB ;
WATSON, GM ;
TRUITT, J .
JOURNAL OF APPLIED PHYSICS, 1962, 33 (09) :2682-&
[8]   INTERDIFFUSION OF GASES IN A LOW-PERMEABILITY GRAPHITE .2. INFLUENCE OF PRESSURE GRADIENTS [J].
EVANS, RB ;
WATSON, GM ;
TRUITT, J .
JOURNAL OF APPLIED PHYSICS, 1963, 34 (07) :2020-&
[9]   SOFC technology development at Rolls-Royce [J].
Gardner, FJ ;
Day, MJ ;
Brandon, NP ;
Pashley, MN ;
Cassidy, M .
JOURNAL OF POWER SOURCES, 2000, 86 (1-2) :122-129
[10]   KINETICS AND MECHANISMS OF THE 2 OPPOSING REACTIONS OF THE EQUILIBRIUM CO + H2O = CO2 + H21 [J].
GRAVEN, WM ;
LONG, FJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1954, 76 (10) :2602-2607