BaCoO3−δ perovskite-type oxygen carrier for chemical looping air separation, part Ⅰ: Determination of oxygen non-stoichiometry and cyclic stability of oxygen carrier

化学计量学 氧气 钙钛矿(结构) 化学链燃烧 解吸 X射线光电子能谱 分析化学(期刊) 空气分离 化学 活化能 化学工程 材料科学 极限氧浓度 物理化学 结晶学 有机化学 色谱法 热力学 吸附 工程类 物理
作者
Ganwei Cai,Cong Luo,Ying Zheng,Dingshan Cao,Tong Luo,Xiaoshan Li,Fan Wu,Liqi Zhang
出处
期刊:Separation and Purification Technology [Elsevier]
卷期号:302: 121972-121972 被引量:5
标识
DOI:10.1016/j.seppur.2022.121972
摘要

Chemical looping air separation (CLAS) is a cost-effective high-temperature air separation technology, and finding suitable oxygen carriers with high oxygen selectivity and capacity is of vital importance to it. Perovskite-type oxides have been extensively studied as oxygen carriers due to their high oxygen selectivity. In this work, BaCoO3-δ perovskite oxide with large oxygen capacity was proposed as an excellent oxygen carrier for CLAS. BaCoO3-δ perovskite powder was synthesized through a sol–gel method, and the determination of oxygen non-stoichiometry and cyclic stability of BaCoO3-δ was investigated via thermogravimetric analysis (TGA), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS). Results indicated that the oxygen non-stoichiometry of BaCoO3-δ was a function of temperature and oxygen partial pressure, and the empirical formula was determined by linear fitting in the range of δ less than 0.5. The standard enthalpy change and standard entropy change of the oxygen desorption reaction were 169.43 kJ/mol and 156.19 kJ/(mol·K) at δ of 0.38, which increased to 292.58 kJ/mol and 298.81 kJ/(mol·K) at δ of 0.47, respectively. The oxygen desorption amount and desorption rate of BaCoO3-δ remained extremely stable during 50 cycles at 875℃, with an oxygen capacity of approximately 0.018 g O2/g BaCoO3 of each cycle. The kinetics of the oxygen desorption process of BaCoO3-δ perovskite was described using the 3-D diffusion Jander model, and the obtained values of apparent activation energy (Ea) and pre-exponential factor (A) were 209.79 kJ/mol and 1.93E06, respectively. Further results indicated that BaCoO3-δ demonstrated a hexagonal perovskite phase, the desorbed oxygen was provided by lattice oxygen in perovskite, the crystal structure remained stable during cycles, and the micro-morphology slightly changed after 50 cycles.
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