Novel mixed conducting SrSc₀.₀₅Co₀.₉₅O₃₋δ ceramic membrane for oxygen separation

• Published in: AIChE journal Vol. 53; no. 12; pp. 3116 - 3124
• Main Authors: Zeng, Pingying, Ran, Ran, Chen, Zhihao, Gu, Hongxia, Shao, Zongping, Liu, Shaomin
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.12.2007; Wiley Subscription Services
• Subjects: Applied sciences; ceramic membrane; Chemical engineering; Exact sciences and technology; mixed conducting; oxygen separation; perovskite; Sintering, pelletization, granulation; Solid-solid systems; SrSc0.05Co0.95O3-δ; Electrical conductivity; perovskite; ceramic membrane; Doping; Permeation; Srsc0.05Co0.95O3-δ; oxygen separation; Partial pressure; mixed conducting; Sintering; Pressing; Kinetics; Thermodynamic properties; Diffusion; Ceramic materials; Activation energy; Inorganic membrane
• ISSN: 0001-1541; 1547-5905
• DOI: 10.1002/aic.11334

A novel perovskite-type mixed-conducting oxide of SrSc₀.₀₅Co₀.₉₅O₃₋δ (SSC) was synthesized by a combined EDTA-citrate complexing method. The 5 mol % of Sc³⁺ doping into the B-site of SrCoO₃₋δ (SC) through the sol-gel synthesis effectively stabilized the oxygen vacancy disordered cubic perovskite structure of the oxide, and simultaneously resulted in a substantial increase of the electrical conductivity. The oxide was fabricated into dense ceramic membrane for oxygen separation by pressing/sintering process. The oxygen permeation flux of the SSC membrane and the rate-determination step of the permeation process were investigated between 750 and 900°C. The experimental results demonstrated that SSC is a promising membrane for oxygen separation with ultrahigh permeation fluxes, compared favorably with reported high oxygen semipermeable Ba₀.₅Sr₀.₅Co₀.₈Fe₀.₂O₃₋δ and SrCo₀.₈Fe₀.₂O₃₋δ membranes under air/helium gradient. At the condition of reduced temperature and low oxygen partial pressure at the sweep side atmosphere, the permeation process was found to be rate-determined mainly by the slow oxygen surface exchange kinetics at the air (feed) side membrane surface based on the single cell oxygen permeation study. The activation energy for the oxygen surface exchange and oxygen bulk diffusion was found to be around 126 kJ mol⁻¹ and <=62.1 kJ mol⁻¹, respectively. © 2007 American Institute of Chemical Engineers AIChE J, 2007