纳滤
膜
聚酰亚胺
渗透
化学工程
材料科学
溶剂
相位反转
高分子化学
化学
纳米技术
有机化学
图层(电子)
工程类
渗透
生物化学
作者
Feng Gan,Senjie Jiang,Jinli Zhou,Junkang Wang,Jiaxiang Wen,Jinpeng Mo,Shaobo Han,Long Fan,Ningbo Yi,Yancheng Wu
标识
DOI:10.1016/j.eurpolymj.2022.111702
摘要
Polyimide-based nanofiltration membranes (NF) featuring customizable chemical structure and outstanding comprehensive performance have garnered tremendous interest for potential applications in ions rejection. Coordinated interactions can build supramolecular networks in polyimide that reshuffle phase separation behavior during membrane formation, thus conferring microstructural flexibility to nanofiltration membranes. In this paper, novel nanofiltration membranes were prepared by constructing dual coordination interactions in polyimide, and the structures were confirmed by NMR, FTIR, EDX, and XPS analyses. As expected, the skin and supporting layers of the PI-based NF membranes can be controlled by designing coordination conditions during membrane formation. A promising result is that the resulted NF membranes occur higher reject of metal ions than the pristine membranes prepared by conventional non-solvent induced phase separation methods. The optimized performance showed significantly higher permeability for removing Mg2+ ions, giving water permeance of 477.7 L m−2 h−1·bar−1 and a rejection of over 80%. Moreover, the resulted PI-based NF membranes occur better solvent resistance than the pristine NF membranes due to the enhanced coordination structures. As a preliminary study, this work gives a new strategy to regulate the microstructure of nanofiltration membranes, promising further potential for applications in ion removal.
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