Synergetic integration of a methanol steam reforming cell with a high temperature polymer electrolyte fuel cell

被引:40
|
作者
Ribeirinha, P. [1 ]
Schuller, G. [2 ]
Boauentura, M. [1 ]
Mendes, A. [1 ]
机构
[1] LEPABE, Fac Engn Porto, Rua Roberto Frias, P-4200465 Oporto, Portugal
[2] German Aerosp Ctr DLR, Inst Engn Thermodynam, D-70569 Stuttgart, Germany
关键词
Methanol steam reforming; HT-PEMFC; Heat integration; H-2; production; PERFORMANCE; HYDROGEN; COMBUSTOR; PRESSURE; CATALYST; MEAS;
D O I
10.1016/j.ijhydene.2017.01.172
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 this work an integrated unit, combining a methanol steam-reforming cell (MSR-C) and a high temperature polymer electrolyte membrane fuel cell (HT-PEMFC) was operated at the same temperature (453 K, 463 K and 473 K) allowing thermal integration and increasing the system efficiency of the combined system. A novel bipolar plate made of aluminium gold plated was built, featuring the fuel cell anode flow field in one side and the reformer flow field on the other. The combined unit (MSR-C/HT-PEMFC) was assembled using Celtec P2200N MEAs and commercial reforming catalyst CuO/ZnO/Al2O3 (BASF RP60). The water/methanol vaporisation originates oscillations in the vapour flowrate; reducing these oscillations increase the methanol conversion from 93% to 96%. The MSR-C/HT-PEMFC showed a remarkable high performance at 453 K. The integrated unit was operated during ca. 700 h at constant at 0.2 A cm(-2), fed alternately with hydrogen and reformate at 453 K and 463 K. Despite the high operating temperature, the HT-PEMFC showed a good stability, with an electric potential difference decreasing rate at 453 K of ca. 100 mu V h(-1). Electrochemical impedance spectroscopy (EIS) analysis revealed an overall increase of the ohmic resistances and charge transfer resistances of the electrodes; this fact was assigned to phosphoric acid losses from the electrodes and membrane and catalyst particle size growth. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:13902 / 13912
页数:11
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