Hydrogen generation in a Pd membrane fuel processor: assessment of methanol-based reaction systems

被引:73
作者
Harold, MP
Nair, B
Kolios, G
机构
[1] Univ Houston, Dept Chem Engn, Houston, TX 77204 USA
[2] Univ Stuttgart, Lehrstuhl & Inst Chem Verfahrenstech, D-70119 Stuttgart 1, Germany
关键词
membranes; reaction engineering; energy; mathematical modeling; hydrogen; fuel cells; fuel processing;
D O I
10.1016/S0009-2509(03)00105-2
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The feasibility of a Pd membrane fuel processor that integrates several methanol-based chemistries and hydrogen purification steps is assessed. The assessment involves membrane reactor simulations to determine the effects of operating and design parameters on performance metrics including hydrogen utilization, hydrogen productivity, device volume, and Pd requirements. Methanol decomposition (direct and oxidative) on Pd/SiO2, methanol steam reforming (MSR) on Cu/ZnO/Al2O3, and methanol partial oxidation (MPOX) on Cu/Al2O3 are evaluated. The membrane reactor model includes detailed treatments of the catalytic kinetics from the literature, accounts for reaction on the Pd membrane and hydrogen permeation inhibition by site blockage, among other features. The simulations reveal that a maximum in the hydrogen productivity occurs at an intermediate value of the space velocity, implying a trade-off between reactor size, methanol conversion and hydrogen utilization. The assessment involves a determination of the Pd membrane surface to reactor volume ratio that maximizes productivity and the requisite Pd to realize that productivity. We show that MSR on Cu/ZnO and MPOX on Cu are promising reaction systems to practice the membrane concept for fuel processing, whereas direct methanol decomposition is reaction limited, making it infeasible. Several approaches for improving membrane fuel processor performance are evaluated and discussed. We show that oxygen addition can increase the hydrogen productivity in the Pd system, while water addition is beneficial for the MPOX system. The extent of enhancement in both cases depends on supply rate and kinetic factors. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2551 / 2571
页数:21
相关论文
共 62 条
[1]   Partial oxidation of methanol to produce hydrogen over Cu-Zn-based catalysts [J].
Alejo, L ;
Lago, R ;
Pena, MA ;
Fierro, JLG .
APPLIED CATALYSIS A-GENERAL, 1997, 162 (1-2) :281-297
[2]   Methanol-induced hydrogen permeation through a palladium membrane [J].
Amandusson, H ;
Ekedahl, LG ;
Dannetun, H .
SURFACE SCIENCE, 1999, 442 (02) :199-205
[3]   EFFECTS OF HIGH-CONCENTRATION CO AND CO2 ON HYDROGEN PERMEATION THROUGH THE PALLADIUM MEMBRANE [J].
AMANO, M ;
NISHIMURA, C ;
KOMAKI, M .
MATERIALS TRANSACTIONS JIM, 1990, 31 (05) :404-408
[4]   On board hydrogen purification for steam reformation PEM fuel cell vehicle power plants [J].
Amphlett, JC ;
Mann, RF ;
Peppley, BA .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 1996, 21 (08) :673-678
[5]   Applications of catalytic inorganic membrane reactors to refinery products [J].
Armor, JN .
JOURNAL OF MEMBRANE SCIENCE, 1998, 147 (02) :217-233
[6]   ADSORPTION OF HYDROGEN ON PD(100) [J].
BEHM, RJ ;
CHRISTMANN, K ;
ERTL, G .
SURFACE SCIENCE, 1980, 99 (02) :320-340
[7]   KINETICS OF CO OXIDATION ON SINGLE-CRYSTAL PD, PT, AND IR [J].
BERLOWITZ, PJ ;
PEDEN, CHF ;
GOODMAN, DW .
JOURNAL OF PHYSICAL CHEMISTRY, 1988, 92 (18) :5213-5221
[8]  
BERLOWITZ PJ, 2000, 2000010003 SAE, P8
[9]  
BRINKMAN HW, 1999, AM CERAMIC SOC B
[10]  
Brown LF, 2001, INT J HYDROGEN ENERG, V26, P381, DOI 10.1016/S0360-3199(00)00092-6