High H2 permeability in F-doped BaZr0.7Ce0.2Y0.1O3-δ perovskite membranes via thermodynamic controlled sintering

被引:0
|
作者
Gu, Zhenbin [1 ]
Tan, Jinkun [1 ]
Zhou, Haoli [1 ]
Liu, Zhengkun [1 ,2 ]
Ge, Lin [3 ]
Zhang, Guangru [1 ,2 ]
Jin, Wanqin [1 ]
机构
[1] Nanjing Tech Univ, Coll Chem Engn, State Key Lab Mat Oriented Chem Engn, Nanjing, Peoples R China
[2] Nanjing Tech Univ, Quzhou Membrane Mat Innovat Inst, Quzhou, Peoples R China
[3] Nanjing Tech Univ, Coll Mat Sci & Engn, Nanjing, Jiangsu, Peoples R China
关键词
anion doping; elements evaporation; hydrogen separation; MPEC; perovskite; HYDROGEN PERMEATION; SEPARATION PERFORMANCE; ELECTROLYTE MEMBRANES; CONDUCTIVITY; TEMPERATURE; OXIDES; MICROSTRUCTURE; STABILITY; TRANSPORT;
D O I
10.1002/aic.18670
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A raw hydrogen mixture frequently results in a reduction in conversion efficiency and the generation of undesired by-products. The application of advanced membrane technology has the potential to offer an economically viable solution for the recovery of hydrogen from such mixtures. BaZr1-x-yCexYyO3-delta is increasingly regarded as an optimal perovskite hydrogen permeable membrane. Nevertheless, the main drawback to its use in a larger scale is the extremely low hydrogen permeability and stability. An original perovskite material is proposed in this study, BaZr0.7Ce0.2Y0.1O3-delta-Fx. A thermodynamic-controlled sintering strategy (TCS) has been employed to inhibit the evaporation of metals from ceramic solids. The TCS directly caused the hydrogen permeation flux to reach 1.07 ml<middle dot>min-1 cm-2, representing a fourfold improvement. Furthermore, F-doping demonstrated enhanced performance at low and medium temperatures. The aforementioned successful strategy provides an effective path for the tailoring of perovskite materials and promotes its application for the industrial-scale separation of hydrogen.
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页数:11
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