Reduction-Tolerant Oxygen-Permeable Perovskite-Type Oxide Sr0.7Ba0.3Fe0.9Mo0.1O3-δ

被引:40
作者
Dong, Xueliang [1 ]
Jin, Wanqin [1 ]
Xu, Nanping [1 ]
机构
[1] Nanjing Univ Technol, Coll Chem & Chem Engn, State Key Lab Mat Oriented Chem Engn, Nanjing 210009, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
MIXED-CONDUCTING MEMBRANES; FUEL-CELLS; STRUCTURAL STABILITY; CHEMICAL EXPANSION; ANODE MATERIALS; CERAMIC MEMBRANES; PERFORMANCE; PERMEATION; METHANE; CO2;
D O I
10.1021/cm903862y
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
The mixed ionic-electronic conducting (MIEC) materials that have been developed for catalytic membrane reactors are vulnerable to a reducing atmosphere, especially H-2. We reported on a MIEC oxide, Sr0.7Ba0.3Fe0.9Mo0.1O3-delta (SBFM), with a cubic perovskite structure (a = 3.91 angstrom at room temperature). SBFM can maintain full perovskite structure in a 5 vol % H-2/He atmosphere at 900 degrees C even for 50 h. The high reduce-tolerant property was mainly attributed to the synergistic effect between Mo(VI)/Mo(V) and Fe3+/Fe2+ couples. SBEM also exhibited good tolerance to a CO2 atmosphere at high temperature (>= 900 degrees C) but reacted with CO2 at relatively low temperature (<800 degrees C). The introduction of Mo ion into the Fe site greatly improved the thermal stabilization of the SBFM oxide. The average thermal expansion coefficients in nitrogen atmosphere were 12.8 x 10(-6) and 20.8 x 10(-6)degrees C-1 in the temperature ranges of 200-600 and 600-900 degrees C, respectively. At 900 degrees C, the oxygen permeation flux of SBEM membrane (1 mm in thickness) was 4.39 x 10-7 mol cm(-2) s(-1). The oxygen permeation activation energy (E-a) was 42 kJ mol(-1), which was significantly lower than that of commonly used MIEC membranes.
引用
收藏
页码:3610 / 3618
页数:9
相关论文
共 42 条
[1]  
Adler SB, 2001, J AM CERAM SOC, V84, P2117, DOI 10.1111/j.1151-2916.2001.tb00968.x
[2]  
[Anonymous], ANGEW CHEM
[3]   Influence of CO2 on the oxygen permeation performance and the microstructure of perovskite-type (Ba0.5Sr0.5)(Co0.8Fe0.2)O3-δ membranes [J].
Arnold, Mirko ;
Wang, Haihui ;
Feldhoff, Armin .
JOURNAL OF MEMBRANE SCIENCE, 2007, 293 (1-2) :44-52
[4]   Ceramic membrane reactor for converting methane to syngas [J].
Balachandran, U ;
Dusek, JT ;
Maiya, PS ;
Ma, B ;
Mieville, RL ;
Kleefisch, MS ;
Udovich, CA .
CATALYSIS TODAY, 1997, 36 (03) :265-272
[5]  
Bouwmeester H.J., 1996, FUNDAMENTALS INORGAN
[6]   Dense ceramic membranes for methane conversion [J].
Bouwmeester, HJM .
CATALYSIS TODAY, 2003, 82 (1-4) :141-150
[7]   Effects of sintering atmospheres on sintering behavior, electrical conductivity and oxygen permeability of mixed-conducting membranes [J].
Chang, Xianfeng ;
Zhang, Chun ;
Dong, Xueliang ;
Zhou, Wei ;
Jin, Wanqin ;
Shao, Zongping ;
Xu, Nanping .
JOURNAL OF MEMBRANE SCIENCE, 2008, 316 (1-2) :128-136
[8]   Match of thermal performances between the membrane and the support for supported dense mixed-conducting membranes [J].
Chang, Xianfeng ;
Zhang, Chun ;
Jin, Wanqin ;
Xu, Nanping .
JOURNAL OF MEMBRANE SCIENCE, 2006, 285 (1-2) :232-238
[9]   Conversion of methane to syngas by a membrane-based oxidation-reforming process [J].
Chen, CS ;
Feng, SJ ;
Ran, S ;
Zhu, DC ;
Liu, W ;
Bouwmeester, HJM .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (42) :5196-5198
[10]   Chemical expansion, crystal structural stability, and oxygen permeability of SrCo0.4Fe0.6-xAlxO3-δ oxides [J].
Dong, Xueliang ;
Xu, Zhi ;
Chang, Xianfeng ;
Zhang, Chun ;
Jin, Wanqin .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2007, 90 (12) :3923-3929