Model development and validation of hydrogen transport through supported palladium membranes

被引:13
作者
Bhargav, Atul [1 ]
Jackson, Gregory S. [1 ]
Ciora, Richard J., Jr. [2 ]
Liu, Paul T. K. [2 ]
机构
[1] Univ Maryland, Dept Mech Engn, College Pk, MD 20742 USA
[2] Media & Proc Technol Inc, Pittsburgh, PA 15238 USA
关键词
Palladium membrane; Porous substrate; H-2; purification; Micro-kinetic modeling; STAINLESS-STEEL MEMBRANES; OXIDE FUEL-CELLS; PD-AG ALLOYS; COMPOSITE MEMBRANES; PHASE-TRANSITION; HIGH-TEMPERATURE; MASS-TRANSFER; N-VALUE; PERMEATION; THIN;
D O I
10.1016/j.memsci.2010.03.041
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Porous matrices are often used to provide structural support to thin Pd-based metallic membranes in H-2 separation applications. Optimizing such composite membranes requires detailed understanding of all possible rate-controlling processes including surface and bulk processes in the metal and diffusion of gases through the porous media. In the work described in this paper, we fabricate a composite membrane by depositing a thin (similar to 5-6 mu m) Pd film on a porous alpha-Al2O3 tube and then measure the H-2 permeance of this composite membrane over a range of operating conditions. The rate-controlling processes for the H-2 permeation are evaluated with a computational model which combines a detailed thermo-kinetic Pd-H-2 interaction model and a porous media transport model. The Pd-H-2 thermo-kinetic model is validated against literature data, and the porous media transport model is independently calibrated using experimental measurements. The combined composite membrane model gives good agreement with experiments over a large range of temperatures (250-450 degrees C) and H-2 partial pressures (100-385 kPa). This validated model is then used to analyze the importance of design parameters such as Pd thickness and support micro-structure on H-2 flux through the membrane. These parametric studies will also aid in assessing trade-offs between membrane structural robustness and overall performance. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:123 / 132
页数:10
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