Effects of carbon dioxide-induced plasticization on the gas trans-port properties of glassy polyimide membranes

被引:102
作者
Kanehashi, Shinji
Nakagawa, Tsutomu
Nagai, Kazukiyo
Duthie, Xavier
Kentish, Sandra
Stevens, Geoff
机构
[1] Meiji Univ, Dept Appl Chem, Tama Ku, Kawasaki, Kanagawa 2148571, Japan
[2] Univ Melbourne, Dept Chem & Biomol Engn, Cooperat Res Ctr Greenhouse Gas Technol CO2CRC, Melbourne, Vic 3010, Australia
关键词
glassy polymer; plasticization; carbon dioxide; permeability; solubility; diffusivity; CHEMICAL CROSS-LINKING; FLUORINATED POLYIMIDES; PERMEABILITY; SOLUBILITY; SEPARATION; SORPTION; PERMSELECTIVITY; SUPPRESSION; VOLUMES; FILMS;
D O I
10.1016/j.memsci.2007.04.012
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The time dependence of carbon dioxide (CO2) transport properties, such as permeability, solubility, and diffusivity, in glassy polyimide membranes was investigated in terms of membrane preparation protocols (i.e., casting solvent and thermal treatment). The polyimide used was 6FDA-TeMPD (4,4-(hexafluoroisopropylidene) diplithalic anhydride) (6FDA)-2,3,5,6-tetramethyl-1,4-phenylene-diamine (TeMPD). The time dependence of C02 permeability in the as-cast 6FDA-TeD4PD membranes prepared from tetrahydrofuran and dichloromethane showed typical CO2-induced plasticization at pressures over 10 atm. The critical plasticization pressure at which CO2-induced plasticization begins to affect the gas permeability shifted from nearly 10-30 atm after heat treatment. The increase in CO2 permeability upon plasticization is mostly caused by an increase in C02 diffusivity. Furthermore, we found that regardless of the membrane preparation protocol, there is a critical CO2 diffusivity of 73 5 x 10-8 CM2/S at the plasticization pressure in 6FDA-TeMPD membranes. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:147 / 155
页数:9
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