Abstract
The increasing demand for lithium in energy storage systems and electronic devices has highlighted the critical need for efficient and selective separation strategies, particularly from salt-lake brines and pre-concentrated lithium-rich streams, which contain high concentrations of competing cations such as Mg2+, Ca2+, Na+, and K+. In this study, a core-shell structured magnetic poslymer adsorbent functionalized with crown ether moieties (MNPs@PS@(PVBC-g-PGMA)-2M12C4) was systematically engineered for the selective recognition and recovery of Li+ ions. The adsorbent was synthesized by grafting 2-hydroxymethyl-12-crown-4 ether (2M12C4) onto a PGMA-modified magnetic polystyrene substrate via surface-initiated radical polymerization. The resulting adsorbent exhibited a rough spherical morphology with an average diameter of 260 nm, excellent surface functionality, and rapid magnetic responsiveness. Batch adsorption experiments revealed a maximum Li+ adsorption capacity of 10.62 mg g−1, with equilibrium reached within 120 min. Kinetic and isotherm analyses indicated that monolayer chemisorption was governed by host-guest interactions between Li+ and the crown ether cavities. Notably, the adsorbent exhibited high selectivity for Li+ over coexisting cations, with selective separation coefficients (α1) exceeding 6.0, and demonstrated excellent recyclability, retaining 96.83% of its initial adsorption capacity after eight consecutive cycles. These results underscore the potential of the crown ether-grafted magnetic polymer microspheres as robust and reusable platforms for lithium recovery from complex aqueous environments.
| Original language | English |
|---|---|
| Pages (from-to) | 14012-14023 |
| Number of pages | 12 |
| Journal | New Journal of Chemistry |
| Volume | 49 |
| Issue number | 32 |
| DOIs | |
| Publication status | Published - 11 Aug 2025 |
| Externally published | Yes |
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