High stability and oxygen permeability are two prominent requirements for the oxygen transport membrane candidates used as industrialization. Herein, we report several composite membranes based on xwt.%Ce0.9Pr0.1O2- (CPO)-(100x)wt.%Pr0.6Sr0.4Fe0.8Al0.2O3- (PSFAO) (x = 50, 60 and 75) prepared via a modified Pechini method. Oxygen permeability test reveals that the 60CPO-40PSFAOcomposition exhibits the highest oxygen permeability. The oxygen permeation flux through the optimal uncoated 0.33 mm-thickness 60CPO-40PSFAO composite can reach 1.03 mL cm -2 min -1 (over the general requirement value of 1 mL cm -2 min -1 ) in air/He atmosphere at 1000 °C. In situ XRD performance confirms the optimal 60CPO-40PSFAO sample shows excellent stability in CO2-containing atmospheres. The 60CPO-40PSFAO membrane still exhibits simultaneously excellent oxygen permeability and phase stability after operating for over 100 h at air/CO2 condition at 1000 °C, which further indicates that the 60CPO-40PSFAO composite is likely to be used for oxygen supply in CO2 capture.
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ABSTRACT:Ceramic dual-phase oxygen transport membranes with the composition of 60wt.% Ce0.9Pr0.1O2-δ-40wt.%Pr0.6Sr0.4Fe1-xAlxO3-δ (x = 0.05, 0.1, 0.2, 0.3, 0.4, 0.6, 0.8, 1.0) (60CPO-40PSF1-xAxO) based on 60Ce0.9Pr0.1O2-δ-40Pr0.6Sr0.4FeO3-δ doped Al was successfully synthesized through a modified Pechini method. Crystal structure, surface microtopography and oxygen permeability are investigated systematically. The cell parameters of perovskite phase first increased and then decreased with the increase of Al content, which is related to the radius of the Al 3+ and the formation of impurity phase.As x ranges from 0.1 to 0.8, the oxygen permeability of the materials first increases and then decreases, and the maximum value of oxygen permeation rate for 60CPO-40PSF1-xAxO membranes with 0.4mm thickness at 1000 °C is 1.12 mL min -1 cm -2 when x = 0.4. XRD measurements revealed high temperature stability and CO2-tolerant property of the dual-phase composites. The partial replacement of Fe 3+ /Fe 4+ by Al 3+ causes the material not only to exhibit good stability, but also to increase the oxygen permeability of the membranes.
Polycrystalline bulks of Bi 2 Sr 2 Ca 1−x K x Cu 2.0 O 8+δ (Bi-2212) with x = 0, 0.05, 0.10 and 0.15 were fabricated by the spark plasma sintering technique. The influences of K doping on the microstructures, electronic structures, as well as the related superconducting properties, were systematically investigated. The XRD analyses confirmed that K + ions have successfully substituted into the matrix of Bi-2212, and lead to a systematical change of lattice parameters. Due to the change of thermodynamic properties, bulks with higher density, larger grain size and better texture structures were obtained after doping. Therefore, ac susceptibility measurement revealed the optimization of intergrain connections, which lead to the optimization of both selfand in-field critical current density, J c of this system. The optimization of microstructures also caused the enhancement of surface pinning. Based on the enhancements of both intergrain connections and flux pinning properties, an obvious improvement of critical current density was obtained with the optimal doping content of K = 0.05. Meanwhile, Bi-2212 single filament tapes with K doping content of 0 and 0.05 were also fabricated by the powder-in-tube process. The XRD patterns also proved the successful doping of K ions in the Bi-2212 matrix. The critical current density J c , measured by the transport method under the magnetic field from 0 to 20 T at 4.2 K, proved the effectiveness of K doping on the enhancement of flux pinning properties of Bi-2212.
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