聚酰胺
材料科学
膜
单体
化学工程
离子
聚合物
高分子化学
复合材料
有机化学
化学
生物化学
工程类
作者
Cheng‐Ye Zhu,Jinbo Li,Jia‐Hui Xin,Hui Fan,Yu Fang,Chao Zhang,Hao‐Cheng Yang,Hong‐Qing Liang,Zhikang Xu
标识
DOI:10.1002/adfm.202509846
摘要
Abstract Devising polyamide membranes with favorable pore size and surface charge is highly promising for boosting their ion‐sieving performance. Despite tremendous achievements, existing polyamide membranes suffer from limited pore size tunability and highly negative charges due to a haphazard or nonoptimized choice of monomer concentrations, significantly locking their ion‐sieving potential, especially for different ion species. Here, a straightforward strategy is proposed to synthesize a series of highly selective polyamide membranes with customized ion‐sieving performance through deciphering the maze of monomer concentrations and ratios to engineer pore size and charge density and systematically elucidating the impact of structure on performance. Beyond conventional concentration ranges, individual increases of either acyl chloride or amine monomer concentration can be harnessed to produce carboxy‐rich or amino‐rich polyamide membranes with enhanced charge group density, demonstrating improved selectivity for mono/divalent anions or cations, respectively. Notably, the simultaneous elevation of both monomer concentrations yields polyamide membranes with the highest amide bond density and smallest pore size, achieving ultrahigh selectivity above 100 for both ion types. Moreover, the optimal polyamide membranes demonstrate superior and durable Li + /Mg 2+ selectivity ranging from 79 to 366 toward simulated salt‐lake brines across varying salinities, Li + /Mg 2+ ratios, and operating pressures.
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