Hydrogen permeation through the Pd-Nb-Pd composite membrane: Surface effects and thermal degradation

被引:38
作者
Alimov, Vasily N. [1 ]
Hatano, Yuji [2 ]
Busnyuk, Andrei O. [1 ]
Livshits, Daniil A. [3 ]
Notkin, Mikhail E. [1 ]
Livshits, Alexander I. [1 ]
机构
[1] Bonch Bruevich Univ, St Petersburg 191186, Russia
[2] Toyama Univ, Hydrogen Isotope Res Ctr, Toyama 9308555, Japan
[3] Innolume GmbH, D-44263 Dortmund, Germany
基金
日本学术振兴会;
关键词
Hydrogen separation; Composite membranes; Niobium; Palladium; PLASMA-DRIVEN SUPERPERMEATION; HIGH-TEMPERATURE STABILITY; METAL MEMBRANES; INTERMEDIATE LAYER; IMPROVEMENT; LIFETIME; FLUX;
D O I
10.1016/j.ijhydene.2011.04.016
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The composite membranes based on Group 5 metals are capable of H-2 separation with the high speed and infinite selectivity. The chemical and thermal stability are critical issues for the application of such membranes in the field of hydrogen energy. In order to understand the degradation mechanisms, the H-2 permeation through composite Pd-2 mu m-Nb-100 mu m-Pd-2 mu m membranes was investigated in a very wide pressure range: (10(-5)-10(4)) Pa. At higher pressures the surface contaminations only moderately decreased the permeation. However the permeation experiments at lower pressures demonstrated that an orders of magnitude change in the probability of H-2 molecule dissociative sticking is actually hidden behind this relatively moderate effect. The membranes poisoned by the surface contaminations could be recovered by their exposure to O-2 at (300-400) degrees C. Heating at temperature higher than 500 degrees C resulted in the irreversible decrease of permeation and in the pronounced change of permeation behavior at the variation of H-2 pressure. An extremely high permeation was observed at lower pressures at the clean surface of Pd coating. That allows developing an effective membrane pump for hydrogen isotopes. Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:7737 / 7746
页数:10
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