Preparation, characterization and stability of vanadium/Y2O3-stabilized ZrO2 composite membranes under different atmospheres

被引:5
|
作者
Park, Jung Hoon [1 ]
Magnone, Edoardo [1 ]
Jeon, Sung Il [1 ]
Baek, Il Hyun [1 ]
机构
[1] Korea Inst Energy Res, Climate Change Technol Res Div, Green House Gas Res Ctr, Taejon 305343, South Korea
关键词
Hydrogen permeation; Composite membrane; Vanadium; Y2O3 -stabilized ZrO2 ceramic phase; Processing parameters; HYDROGEN PERMEABILITY; THERMAL-DECOMPOSITION; VANADIUM ALLOYS; FUEL-CELLS; SEPARATION; PERMEATION; TRANSPORT; REACTOR; SURFACE; BINDER;
D O I
10.1016/j.memsci.2011.01.010
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In this experimental work vanadium/Y2O3-stabilized ZrO2 composite membrane was successfully fabricated by a two-step sintering process. The formation of a well-defined ceramic metal composite membrane was confirmed under high vacuum sintering conditions. Their surface morphology, stability and structural properties were studied as a function of temperature up to 1100 degrees C by thermogravimetry, differential thermal analysis, scanning electron microscopy, energy dispersive X-ray spectroscopy, and X-ray diffraction analysis. Significant differences were observed in the crystalline structure of the vanadium/Y2O3-stabilized ZrO2 composite membranes when they were treated at high temperature in different atmospheres (vacuum, air, hydrogen, nitrogen, and helium). The first hydrogen permeation investigation of vanadium/Y2O3-stabilized ZrO2 composite membrane is reported. Preliminary hydrogen permeation experiments have been confirmed that hydrogen flux was 1.08 ml min(-1) cm(2) for a dense vanadium/Y2O3-stabilized ZrO2 composite membrane (thick: 380 mu m) at 300 degrees C using 100% H-2 as the feed gas. Both high temperature XRD and ex situ study showed deterioration of membranes and the formation of a small amount of vanadium nitride (VNx) and vanadium hydride (VHx) solid solutions under nitrogen and hydrogen gas conditions, respectively. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:149 / 157
页数:9
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