Kinetic demixing and decomposition of oxygen permeable membranes |
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| Affiliation: | 1. Faculty of Electronics, Telecommunications and Informatics, Gdansk University of Technology, Narutowicza 11/12, 80-233, Gdansk, Poland;2. Department of Energy Conversion and Storage, Technical University of Denmark, Risø Campus, Frederiksborgvej 399, DK-4000, Roskilde, Denmark;1. Department of Materials Science and Engineering, Clemson University, Clemson, SC 29634, USA;2. United States Department of Energy, National Energy Technology Laboratory, Morgantown, WV 26507, USA;3. United States Department of Energy, National Energy Technology Laboratory, Pittsburgh, PA 15236, USA;4. Materials Science and Engineering Department, Carnegie Mellon University, Pittsburgh, PA 15213, USA;5. AECOM, Morgantown, WV 26507, USA;1. Materials Science and Engineering Postgraduate Program, UFRN, 59078-970 Natal, Brazil;2. Department of Materials and Ceramic Engineering, University of Aveiro, 3810-193 Aveiro, Portugal;3. Department of Mechanical Engineering, University of Aveiro, 3810-193 Aveiro, Portugal;4. Materials Science and Engineering Postgraduate Program, UFPB, 58051-900 João Pessoa, Brazil;1. School of Metallurgy, Northeastern University, Shenyang, China;2. Liaoning Key Laboratory for Metallurgical Sensor and Technology, Northeastern University, Shenyang, China;1. Department of Materials Science and Metallurgy, University of Cambridge, Cambridge CB3 0FS, UK;2. State Key Laboratory of Advanced Metallurgy University of Science and Technology Beijing, Beijing 100083, PR China |
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| Abstract: | Oxygen flux through La0.5Sr0.5Fe1−xCoxO3−δ (x = 0, 0.5 and 1) membranes has been determined as a function of oxygen partial pressure, temperature and time. The flux was diffusion controlled for low pO2 gradients while larger pO2 gradients caused a surface exchange controlled flux. The activation energy of the oxygen flux varied in the range 67–105 kJ/mol. After about 1 month at 1150 °C in an O2/N2 gradient the membranes were examined for kinetic demixing and decomposition. On the reducing side only the original perovskite phase was observed at the surface, while on the oxidizing side various secondary phases were observed dependent on the composition at the Fe/Co-site and the Sr + La/Fe + Co ratio of the materials. Moreover, kinetic demixing of the main perovskite phase was also observed, particularly near the surfaces. Grain growth and pore coalescence resulting in membrane expansion were also observed in some cases. The present findings are discussed with regard to the long term chemical stability of the membranes. |
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