Enhanced CO2 Resistance for Robust Oxygen Separation Through Tantalum-doped Perovskite Membranes
dc.contributor.author | Zhang, C. | |
dc.contributor.author | Tian, H. | |
dc.contributor.author | Yang, D. | |
dc.contributor.author | Sunarso, J. | |
dc.contributor.author | Liu, J. | |
dc.contributor.author | Liu, Shaomin | |
dc.date.accessioned | 2017-01-30T12:58:50Z | |
dc.date.available | 2017-01-30T12:58:50Z | |
dc.date.created | 2016-02-15T19:30:20Z | |
dc.date.issued | 2016 | |
dc.identifier.citation | Zhang, C. and Tian, H. and Yang, D. and Sunarso, J. and Liu, J. and Liu, S. 2016. Enhanced CO2 Resistance for Robust Oxygen Separation Through Tantalum-doped Perovskite Membranes. ChemSusChem. 9 (5): pp. 505-512. | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/27417 | |
dc.identifier.doi | 10.1002/cssc.201501395 | |
dc.description.abstract |
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. Oxygen selective membranes with enhanced oxygen permeability and CO2 resistance are highly required in sustainable clean energy generation technologies. Here, we present novel, cobalt-free, SrFe1-xTaxO3-d (x=0, 0.025, 0.05, 0.1, 0.2) perovskite membranes. Ta-doping induced lattice structure progression from orthorhombic (x=0) to cubic (x=0.05). SrFe0.95Ta0.05O3-d (SFT0.05) showed the highest oxygen flux rates reaching 0.85mLmin-1cm-2 at 950°C on a 1.0mm-thick membrane. Surface decoration can increase the permeation rate further. Ta inclusion within the perovskite lattice of SrFeO3-d (SF) enhanced the CO2 resistance of the membranes significantly as evidenced by the absence of the carbonate functional groups on the FTIR spectrum when exposed to CO2 atmosphere at 850°C. The CO2 resistance of Ta-doped SF compounds correlates with the lower basicity and the higher binding energy for the lattice oxygen. SFT0.05 demonstrated high stability during long-term permeation tests under 10% CO2 atmosphere. | |
dc.title | Enhanced CO2 Resistance for Robust Oxygen Separation Through Tantalum-doped Perovskite Membranes | |
dc.type | Journal Article | |
dcterms.source.issn | 1864-5631 | |
dcterms.source.title | ChemSusChem | |
curtin.department | Department of Chemical Engineering | |
curtin.accessStatus | Fulltext not available |
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