Ba0.5Sr0.5Co0.8Fe0.2O3-δ ceramic hollow-fiber membranes for oxygen permeation

被引:89
|
作者
Liu, S. [1 ]
Tan, X.
Shao, Z.
da Costa, J. C. Diniz
机构
[1] Univ Queensland, Sch Engn, ARC Ctr Funct Nanomat, Brisbane, Qld 4072, Australia
[2] Shandong Univ Technol, Dept Chem Engn, Zibo 255049, Peoples R China
[3] Nanjing Univ Technol, Coll Chem & Chem Engn, Key Lab Mat Oriented Chem Engn, Minist Educ China, Nanjing 210009, Peoples R China
关键词
air separation; mixed conducting ceramic; hollow-fiber membrane; perovskite membrane;
D O I
10.1002/aic.10966
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Setf-supported asymmetric hollow-fiber membranes of mixed oxygen-ionic and electronic conducting perovskite Ba0.5Sr0.5Co0.8Fe0.2O3-delta (BSCF) were prepared by a combined phase-inversion and sintering technique. The starting inorganic powder was synthesized by combined EDTA-citrate complexing process followed by thermal treatment at 600 degrees C. The powder was dispersed in a polymer solution and then extruded into hollow-fiber precursors through a spinneret. ne fiber precursors were sintered at elevated temperatures to form gastight membranes, which were characterized by SEM and gas permeation tests. Performance of the hollow fibers in air separation was both experimentally and theoretically studied at various conditions. The results reveal that the oxygen permeation process was controlled by the slow oxygen surface exchange kinetics under the investigated conditions. The porous inner surface of the prepared perovskite hollow-fiber membranes considerably favored the oxygen permeation. The maximum oxygen flux measured was 0.031 mol-m(-2).s(-1) at 950 degrees C with the sweep gas flow rate of 0.522 mol(.)m(-2).s(-1). To improve the oxygen flux of BSCF perovskite membranes, future work should be focused on surface modification rather than reduction of the membrane thickness. (c) 2006 American Institute of Chemical Engineers.
引用
收藏
页码:3452 / 3461
页数:10
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