Nonisothermal model for gas separation hollow-fiber membranes

被引:49
作者
Coker, DT
Allen, T
Freeman, BD
Fleming, GK
机构
[1] N Carolina State Univ, Dept Chem Engn, Raleigh, NC 27695 USA
[2] Air Liquide, Houston, TX 77008 USA
[3] Air Liquide, Newport, DE 19804 USA
关键词
D O I
10.1002/aic.690450709
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A model for multicomponent gas separation using hollow-fiber membrane modules is presented that explicitly accounts for heating or cooling inside membrane permeators due to gas expansion. The model permits simulation of countercurrent contacting with permeate purging (or sweep). The numerical approach permits rapid and stable solutions for cases with many components, even when the mixture contains components with widely varying permeability coefficients. Simulation results are presented for natural-gas sweetening, a commercially significant application, using polymer permeation properties similar to those of a high-performance polyimide. For some conditions, temperature decreases from the feed to residue end of the module by as much as 40 degrees C. As CO2 concentration in the feed increases or as stage cut increases, the temperature decrease from feed to residue increases. Relative to an isothermal case, expansion-driven cooling reduces stage cut at a given feed flow rate since gas permeability decreases with decreasing temperature. Neglect of expansion-driven cooling in natural-gas separation simulations can lead to large errors in estimating the amount of feed gas that can be treated to achieve a fixed residue composition. For 30% CO2 feed concentration, if the effective membrane thickness is halved only a 20% increase (rather than almost a factor of 2) in the amount of gas that can be treated per unit area is obtained due to the impact of expansion-driven cooling on gas flux.
引用
收藏
页码:1451 / 1468
页数:18
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