摘要
Precise ion separation is crucial for applications such as wastewater treatment, energy storage, and resource recovery, but challenges arise due to the similar properties of metal ions. To address this, a monomer with crown ether-like properties, o-phenyldioxydiacetyl chloride (OPDC), was synthesized for ion-selective membrane design via interfacial polymerization. The resulting membrane exhibited seven times higher Li+ flux compared to conventional thin-film composite (TFC) membranes. Electrodialysis and crossflow filtration experiments revealed that OPDC-enhanced TFC membranes play a key role in selective Li+ separation. The OPDC monomer enables both chemical complexation and physical sieving, improving Li+/Mg2+ selectivity. Density Functional Theory (DFT) simulation reveals the thermodynamically favorable binding preferences of the OPDC monomer. The strong complexation ability of OPDC towards Mg2+ led to the formation of a stable state, reducing Mg2+ permeability through the membrane and thereby improving the Li+/Mg2+ separation performance of the membrane. This work advances the understanding of ion transport mechanisms and paves the way for the development of ion-selective TFC membranes.
源语言 | 英语 |
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文章编号 | 124165 |
期刊 | Journal of Membrane Science |
卷 | 730 |
DOI | |
出版状态 | 已出版 - 7月 2025 |