Hydrogen production from liquid hydrocarbon fuels for PEMFC application

被引:24
作者
Chen, Yazhong
Xu, Hengyong
Wang, Yuzhong
Jin, Xianglan
Xiong, Guoxing
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Appl Catalysis Lab, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[3] Res Inst Daqing Petrohem Co, Daqing 163000, Peoples R China
关键词
liquid hydrocarbons; prereforming; autothermal reforming; distributed air feed; nickel catalyst; Pd membrane;
D O I
10.1016/j.fuproc.2006.07.007
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Lack of efficient hydrogen storage intermediate has boosted the development of fuel processor or economic onsite hydrogen production techniques for application to proton exchange membrane fuel cell promptly. Aiming to develop onsite hydrogen production techniques for proton exchange membrane fuel cell application using nickel-based reforming catalysts and stainless steel reactors, in this paper, a novel process for H-2 production from liquid hydrocarbon fuels was proposed and experimentally demonstrated on a lab scale. The main operations involved prereforming, autothermal reforming, high temperature water gas shift, low temperature water gas shift and H-2 enrichment by Pd membrane. The results indicated that prereforming introduction prior to autothermal reforming suppressed undesired gas phase reactions efficiently and made reforming reactions perform catalytically and smoothly, which was confirmed by a stable 500 h time-on-stream test of both prereforming and autothermal reforming catalysts. The air distributed feed applied in autothermal reforming reactor coupled the endothermic steam reforming and exothermic catalytic combustion reactions over the catalyst closely, maintaining an appropriate temperature distribution curve for autothermal reforming catalyst bed. During the process of H-2 enrichment by highly H-2 permeable Pd composite membrane, concentration polarization played an important role. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:971 / 978
页数:8
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