聚酰胺
界面聚合
共价键
膜
基质(水族馆)
化学工程
图层(电子)
材料科学
化学
薄膜复合膜
聚合
高分子化学
聚合物
复合材料
有机化学
反渗透
单体
地质学
工程类
海洋学
生物化学
作者
Chengbao Geng,Pei Huang,Fangbo Zhao,Hongxing Dong,Hongyan Niu,Yue Zhou,Jun Shen,Jiaming Zhang
标识
DOI:10.1016/j.memsci.2021.119637
摘要
The weak interfacial force among the substrate with polyamide layer is always a non-ignorable issue for the traditional thin-film composite (TFC) membrane during actual operation. To solve this issue, herein, we have proposed an effective strategy, which is enhancing the long-term separation durability of the TFC membrane by fixing the polyamide layer on the substrate through covalent bonding. To start with, an amino-substituted polyethersulfone (PES-NH2) was synthesized and blended with polyethersulfone (PES) to prepare a hydrophilic PES/PES-NH2 substrate. Next, the amino group in the substrate could effectively react with a part of acyl chloride groups in the organic phase to form the stable covalent bond with the polyamide layer formed by interfacial polymerization. The prepared PES/PES-NH2 TFC membrane possessed a denser polyamide layer with a higher cross-linking degree, as well as exhibited greatly increased separation performance at 0.6 MPa. Significantly, the PES/PES-NH2 TFC membrane still maintained excellent separation performance under a long-term filtration period of 15 days, which is also much longer than the PES TFC membrane. This effective and promising method provides a valuable way to maintain the separation stability of TFC membrane in long-term operation.
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