Development of paper-structured catalyst for application to direct internal reforming solid oxide fuel cell fueled by biogas

被引:25
|
作者
Nguyen, T. G. H. [1 ]
Sakamoto, M. [2 ]
Uchida, T. [2 ]
Doan, D. C. T. [3 ]
Dang, M. C. [3 ]
Tu, P. H. [3 ]
Sasaki, K. [1 ,2 ]
Shiratori, Y. [1 ,2 ]
机构
[1] Kyushu Univ, Dept Hydrogen Energy Syst, Nishi Ku, 744 Motooka, Fukuoka, Fukuoka 8190395, Japan
[2] Kyushu Univ, Int Res Ctr Hydrogen Energy, Nishi Ku, 744 Motooka, Fukuoka, Fukuoka 8190395, Japan
[3] Vietnam Natl Univ Ho Chi Minh City, Inst Nanotechnol, Community 6, Linh Trung Ward, Ho Chi Minh City, Vietnam
关键词
Paper-structured catalyst; (Ce; Zr)O-2; Solid oxide fuel cell; Internal reforming; Biogas; CARBON DEPOSITION; PARTIAL OXIDATION; METHANE; NI; ANODE; DEACTIVATION; FUNDAMENTALS; HYDROCARBONS; CO;
D O I
10.1016/j.ijhydene.2019.02.134
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
A flexible paper-structured catalyst (PSC) that can be applied to the anode of a solid oxide fuel cell (SOFC) was examined for its potential to enable direct internal reforming (DIR) operation. The catalytic activity of three types of Ni-loaded PSCs: (a) without the dispersion of support oxide particles in the fiber network (PSC-A), (b) with the dispersion of (Mg,Al)O derived from hydrotalcite (PSC-B), and (c) with the dispersion of (Ce,Zr)O2-delta (PSC-C), for dry reforming of CH4 was evaluated at operating temperatures of 650-800 degrees C. Among the PSCs, PSC-C exhibited the highest CH4 conversion with the lowest degradation rate. The electrochemical performance of an electrolyte-supported cell (ESC) was evaluated under the flow of simulated biogas at 750 degrees C for cases without and with the PSCs on the anode. The application of the PSCs improved the cell performance. In particular, PSC-C had a remarkably positive effect on stabilizing DIRSOFC operation fueled by biogas. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:10484 / 10497
页数:14
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