Plasticization of ultra-thin polysulfone membranes by carbon dioxide

被引:102
|
作者
Scholes, Colin A. [1 ]
Chen, George Q. [1 ]
Stevens, Geoff W. [1 ]
Kentish, Sandra E. [1 ]
机构
[1] Univ Melbourne, Dept Chem & Biomol Engn, Cooperat Res Ctr Greenhouse Gas Technol CO2CRC, Melbourne, Vic 3010, Australia
基金
澳大利亚研究理事会;
关键词
Gas separation; Polymeric membrane; Ultra-thin; Plasticization; Carbon dioxide; Polysulfone; GLASS-TRANSITION TEMPERATURE; GAS-TRANSPORT PROPERTIES; POLYMER-FILMS; SEPARATION MEMBRANES; FLUE-GASES; SORPTION; PERMEATION; INTERFACE; CAPTURE;
D O I
10.1016/j.memsci.2009.09.036
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Plasticization of gas separation membranes by carbon dioxide permanently alters their performance and increases the possibility of membrane failure. This is amplified in ultra-thin composite membranes, where the active polymeric layer is less than 2 mu m. Here, the plasticization influence of CO2 is measured on ultra-thin polysulfone composite membranes for a range of active layer thicknesses, at four temperatures. The resulting permeability-pressure isotherms demonstrate plasticization occurs for all thicknesses at pressures lower than has been reported for dense membranes. These isotherms were quantitatively fitted with an expanded dual-sorption model that takes into account plasticization of the membrane. The plasticization potential Of CO2 for polysulfone was found to increase with reduced active layer thickness. Similarly, the plasticization potential of CO2 was found to decrease with temperature. These results are consistent with similar research that shows that thin films behave differently to dense membranes. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:208 / 214
页数:7
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