Ion pair extractant selective for LiCl and LiBropen access
- Authors
- Heo, Nam Jung; Oh, Ju Hyun; Li, Aimin; Lee, Kyounghoon; He, Qing; Sessler, Jonathan L.; Kim, Sung Kuk
- Issue Date
- Aug-2024
- Publisher
- Royal Society of Chemistry
- Citation
- Chemical Science, v.15, no.34, pp 13958 - 13965
- Pages
- 8
- Indexed
- SCIE
SCOPUS
- Journal Title
- Chemical Science
- Volume
- 15
- Number
- 34
- Start Page
- 13958
- End Page
- 13965
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/73543
- DOI
- 10.1039/d4sc03760j
- ISSN
- 2041-6520
2041-6539
- Abstract
- Improved methods for achieving the selective extraction of lithium salts from lithium sources, including rocky ores, salt-lake brines, and end-of-life lithium-ion batteries, could help address projected increases in the demand for lithium. Here, we report an ion pair receptor (2) capable of extracting LiCl and LiBr into an organic receiving phase both from the solid state and from aqueous solutions. Ion pair receptor 2 consists of a calix[4]pyrrole framework, which acts as an anion binding site, linked to a phenanthroline cation binding motif via ether linkages. Receptor 2 binds MgBr2 and CaCl2 with high selectivity over the corresponding lithium salts in a nonpolar aprotic solvent. The preference for Mg2+ and Ca2+ salts is reversed in polar protic media, allowing receptor 2 to complex LiCl and LiBr with high selectivity and affinity in organic media containing methanol or water. The effectiveness of receptor 2 as an extractant for LiCl and LiBr under liquid-liquid extraction (LLE) conditions was found to be enhanced by the presence of other potentially competitive salts in the aqueous source phase. An ion pair receptor is reported that is capable of extracting LiCl and LiBr selectively from aqueous phases; the extraction efficiency is enhanced by the presence of other competitive salts.
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