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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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