聚酰亚胺
玻璃化转变
膜
增塑剂
高分子化学
聚合物
吸附
共价键
化学工程
化学
退火(玻璃)
渗透
二氧化碳
材料科学
有机化学
复合材料
吸附
工程类
图层(电子)
生物化学
作者
John D. Wind,Claudia Staudt‐Bickel,Donald R. Paul,William J. Koros
出处
期刊:Macromolecules
[American Chemical Society]
日期:2003-02-22
卷期号:36 (6): 1882-1888
被引量:202
摘要
Solid-state covalent cross-linking of 6FDA-based polyimides with esterification reactions is shown to be effective in stabilizing membranes against CO 2 plasticization up to 40 atm feed pressure. The selection of cross-linking agent has a major impact on the cross-linking degree and the gas transport properties. A generalized cross-linking strategy is presented that enables analysis of the effects of the cross-linking agent structure and thermal treatment on pure gas permeation and sorption for CO 2 and CH 4 at 35 °C. The polyimide 6FDA-DAM:DABA 2:1 was cross-linked with ethylene glycol, 1,4-butylene glycol, 1,4-cyclohexanedimethanol, and 1,4-benzenedimethanol to illustrate these effects. The cross-linking degree is evaluated by a combination of solution 1 H NMR and solid-state IR spectroscopy. The annealing temperature is a significant factor in determining the membrane transport properties, since it affects the polymer chain rigidity and free volume distribution. It is believed that this cross-linking approach can be implemented in an industrial hollow fiber formation process since the reaction is shown to occur in the solid state, well below the glass transition temperature.
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