Oxygen desorption behavior of sol-gel derived perovskite-type oxides in a pressurized fixed bed reactor

Perovskite-type oxides have been considered to be an effective oxygen carrier for producing O-2/CO2 for oxy-fuel combustion application, which is a promising technique for carbon capture and storage. However, the main problem of common perovskite-type oxygen carriers is their relatively low oxygen desorption capacity at atmospheric pressure. Therefore, it is important to develop new oxygen carriers and enhance the reaction pressure to achieve high desorption capacity. In this study, a series of A/beta site substitution Ba1-xSrxCo1-y,FeyO3-delta(x = 0, 0.5, 1; y = 0, 0.2, 1) perovskites were synthesized by solgel method, and the oxygen desorption performance of them was investigated in pressurized fixed bed. The perovskite samples were characterized using X-ray diffraction (XRD), X-ray fluorescence (XRF), X-ray photoelectron spectroscopy (XPS) and Transmission electron microscopy (TEM) measurements. The effect of reaction pressure, temperature and flow rate on the oxygen desorption performance were investigated in details. The results indicated that all of the Ba1-xSrxCo1-y,FeyO3-delta perovskites showed an obvious improvement on oxygen desorption capacity at pressurized conditions. Besides, BaCo03_8 showed the best oxygen desorption performance among theBa(1-x)Sr(x)Co(1-y),FeyO3-delta(x = 0, 0.5, 1; y = 0, 0.2, 1) perovskites. Oxygen desorption amounts of BaCoO3-delta increased by 57.2% and 62.7% under 2 MPa and 3 MPa conditions respectively, comparing to that of it under atmospheric pressure at 850 degrees C. The optimal temperature and WHSV for BaCoO3-delta are 850 degrees C and 176.78 h(-1). XRF and XRD results showed that the elemental contents of perovskites remained after reactions and the crystal structure of perovskites could recover after cyclic process under high pressure calcination. XPS results showed the evolution of oxygen species during oxygen desorption process. (C) 2017 Elsevier B.V. All rights reserved.