聚酰亚胺
膜
氢键
氢
气体分离
聚合物
材料科学
化学工程
增塑剂
氢气净化器
高分子化学
分子
化学
有机化学
复合材料
制氢
工程类
图层(电子)
生物化学
作者
Xiuling Chen,Zhiguang Zhang,Lei Wu,Yanfang Fan,Hongying Tang,Nanwen Li
标识
DOI:10.1016/j.memsci.2022.120575
摘要
To promote polyimide gas transport properties, we propose a facile technique through adjustable hydrogen bonding energy through blending polyimide (6FDA-DABA) containing –COOH groups and Tröger's base (TB) polymer without damaging polymer chemical structures. The hydrogen bonding strength between –OH groups in PI and the N atoms in TB (O–H⋯N) is well tailored via controlled thermal treatment which has been confirmed by molecular simulations. Hydrogen bonding amounts and strength reach maximum within membranes annealed at 120 °C for 16 h, and exhibit CO2/CH4 and H2/CH4 selectivities of 115.0 and 481.8 respectively, surpassing the 2008 upper bound. Contributed by the enhanced hydrogen bonding strength, the membranes annealed at 120 °C for 16 h display excellent CO2 plasticization resistance and physical aging in comparison with pristine PI and TB membranes. Such a approach potentially renders a synthetic membrane applicable for CO2 separation and hydrogen purification at high temperatures.
科研通智能强力驱动
Strongly Powered by AbleSci AI