1 Electroceramics, Fuel Cells and Solid State Chemistry Division, Risø National Laboratory for Sustainable Energy, Technical University of Denmark2 Fuel Cells and Solid State Chemistry Division, Risø National Laboratory for Sustainable Energy, Technical University of Denmark3 Risø National Laboratory for Sustainable Energy, Technical University of Denmark4 unknown5 Department of Energy Conversion and Storage, Technical University of Denmark6 Mixed Conductors, Department of Energy Conversion and Storage, Technical University of Denmark
Ceramic oxygen transport membranes (OTMs) enable selective oxygen separation from air at high temperatures. Among several potential applications for OTMs, the use in (1) oxygen production for oxyfuel power plants and (2) the integration in high-temperature catalytic membrane reactors for alkane upgrading through selective oxidative reactions are of special interest. Nevertheless, these applications involve the direct contact of the membrane surface with carbon-rich atmospheres. Most state-of-the-art permeable membranes are based on perovskites, which are prone to carbonation under operation in CO2-rich environments and/or decomposition in reducing gas environments. The oxygen flux through supported thin film membranes of Ce0.9Gd0.1O1.95−δ (CGO) with 2 mol.% of cobalt was measured for oxygen separation in oxyfuel processes and in syngas production and degradation was compared to perovskite membranes. The CGO membranes consist of a 27 μm-thick gastight CGO layer supported on a porous CGO substrate. The flat surface of the membrane was coated using two different porous catalytic layers aiming to improve the oxygen activation rate on the permeate side while the porous substrate was infiltrated with an oxygen reduction catalyst. Oxygen separation was studied using air as feed and argon/CO2 or argon/CH4 mixtures as sweep gas in the temperature range 750–1000 °C. The supported membrane exhibited a maximum oxygen flux of ca. 5 ml min−1 cm−2 at 1000 °C when diluted methane was used as sweep gas. The CGO membrane showed high stability in CO2 (in contrast to tests on La0.6Sr0.4Co0.2Fe0.8O3−δ (LSCF) membranes) and no detrimental effect on the oxygen flux is observed when CO2 is present in the sweep gas even at temperatures below 800 °C. Moreover, the SEM analysis showed that membrane integrity remained stable after the permeation tests using CO2.
Journal of Membrane Science, 2011, Vol 385-386, p. 154-161