# Regulating the Crystalline Structure and Ion Affinity of Covalent Organic Frameworks for Enhanced Lithium/Magnesium Separation

**Authors:** Chuncai Wang, Shiwen Bao, Yanfeng Gong, Lei Yu, Zizhe Xu, Chul. B. Park, Kunyan Sui, Jun Gao, Xueli Liu

PMC · DOI: 10.3390/biomimetics11030177 · Biomimetics · 2026-03-03

## TL;DR

This paper introduces a method to improve ion separation in membranes by adjusting crystallinity and ion affinity using CO2 drying and crown ether functionalization.

## Contribution

A novel strategy combining ScCO2 drying and 12-crown-4 functionalization to enhance Li+/Mg2+ separation in COF membranes.

## Key findings

- ScCO2 drying increased crystallinity and Li+ flux by 1.5-fold in COF membranes.
- 12-crown-4 functionalization restored selectivity to 187 without reducing Li+ flux.
- The method maintained performance in real salt lake brines.

## Abstract

Selective ion transport is essential for many applications of membrane separation, such as rare metal and high-value element extraction from complex ionic sources. However, efficient regulation of permeability–selectivity remains a major challenge for advanced ionic transport membranes. Herein, we demonstrate that supercritical CO2 (ScCO2) drying combined with crown ether functionalization enables precise modulation of crystallinity and ion-specific affinity in covalent organic framework (COF) membranes. The pristine COF membrane prepared by solution casting was amorphous. Owing to its positively charged framework and sub-nanometer pores, the membrane exhibited a high Li+ transport rate over Mg2+ via a synergistic effect of size exclusion and electrostatic repulsion, resulting in a selectivity of 204. After ScCO2 drying, the crystallinity and structural ordering of the COF membrane were significantly enhanced, leading to a 1.5-fold increase in Li+ flux, accompanied by a moderate decrease in selectivity to 147. To compensate for this trade-off, 12-crown-4 (12C4) was introduced as a Li+ recognition agent into the ScCO2-treated membrane, restoring Li+/Mg2+ selectivity to 187 without compromising Li+ flux. Importantly, the selective Li+ transport performance was maintained in real salt lake brines. This structural–chemical co-regulation strategy provides a versatile approach for optimizing ion transport membranes in complex separation applications.

## Linked entities

- **Chemicals:** 12-crown-4 (PubChem CID 9269), Li+ (PubChem CID 28486), Mg2+ (PubChem CID 888)

## Full-text entities

- **Diseases:** injury to (MESH:D014947)
- **Chemicals:** Ethanol (MESH:D000431), DCM (MESH:D008752), DMSO (MESH:D004121), chloride (MESH:D002712), salt (MESH:D012492), C (MESH:D002244), acetone (MESH:D000096), imine (MESH:D007097), Crown Ether (MESH:D043844), Na+ (MESH:D012964), COF (MESH:D000073396), Magnesium (MESH:D008274), brine (MESH:C017082), Br (MESH:D001966), PTFE (MESH:D011138), 1,3,5-triaminoxybenzidine (-), DMF (MESH:D004126), EB (MESH:D004996), K+ (MESH:D011188), water (MESH:D014867), LiCl (MESH:D018021), MgCl2 (MESH:D015636), 12-CROWN 4-ETHER (MESH:C557123), CO2 (MESH:D002245), 1,3,5-Triformylphloroglucinol (MESH:C000607859), Li (MESH:D008094)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13024126/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC13024126/full.md

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Source: https://tomesphere.com/paper/PMC13024126