Oxygen transport properties of tubular Ce0.9Gd0.1O1.95-La0.6Sr0.4FeO3−d composite asymmetric oxygen permeation membranes supported on magnesium oxide
S. Ovtar; J. Gurauskis; A.B. Haugen; C. Chatzichristodoulou; A. Kaiser; P.V. Hendriksen. Journal of Membrane Science. Volume 523 - 1, pp. 576 - 587.
The oxygen permeation through dense Ce0.9Gd0.1O1.95 - (La0.6Sr0.4)(0.98)FeO3-d dual-phase composite asymmetric membranes supported on a porous MgO tube was studied. The membranes were prepared by thermoplastic extrusion, dip coating, co-sintering and infiltration of a catalyst. Oxygen permeation measurements and electrical conductivity characterization of the membrane were performed as a function of temperature and oxygen partial pressure. The oxygen flux through the membrane in a H-2/air gradient at 850 degrees C reached 15 N ml cm(-2) min(-1). The measured oxygen flux was in good agreement with the theoretically estimated one, taking into account the transport properties of the composite, surface exchange losses, gas diffusion and gas conversion in the MgO support. The performance of the membrane was limited by the surface exchange for the operation in N-2/air, CO2/air and H-2/air at low temperatures and most probably by the porosity of the MgO support for the operation in H-2/air at 850 degrees C. The stability tests of the membrane in CO2/air and H-2/air configurations revealed that an initial degradation of the oxygen flux occurs and it is followed by a relatively stable performance. Post-mortem analysis of the membrane after 900 h of operation did not reveal any significant microstructural degradation of the membrane layer.
The oxygen permeation through dense Ce0.9Gd0.1O1.95 - (La0.6Sr0.4)(0.98)FeO3-d dual-phase composite asymmetric membranes supported on a porous MgO tube was studied. The membranes were prepared by thermoplastic extrusion, dip coating, co-sintering and infiltration of a catalyst. Oxygen permeation measurements and electrical conductivity characterization of the membrane were performed as a function of temperature and oxygen partial pressure. The oxygen flux through the membrane in a H-2/air gradient at 850 degrees C reached 15 N ml cm(-2) min(-1). The measured oxygen flux was in good agreement with the theoretically estimated one, taking into account the transport properties of the composite, surface exchange losses, gas diffusion and gas conversion in the MgO support. The performance of the membrane was limited by the surface exchange for the operation in N-2/air, CO2/air and H-2/air at low temperatures and most probably by the porosity of the MgO support for the operation in H-2/air at 850 degrees C. The stability tests of the membrane in CO2/air and H-2/air configurations revealed that an initial degradation of the oxygen flux occurs and it is followed by a relatively stable performance. Post-mortem analysis of the membrane after 900 h of operation did not reveal any significant microstructural degradation of the membrane layer.