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 ether linkages. Receptor 2 binds MgBr and CaCl with high selectivity over the corresponding lithium salts in a nonpolar aprotic solvent. The preference for Mg and Ca 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.
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http://dx.doi.org/10.1039/d4sc03760j | DOI Listing |
Chem Sci
December 2024
Department of Chemistry, Research Institute of Natural Sciences, Gyeongsang National University Jinju 52828 Korea
[This corrects the article DOI: 10.1039/D4SC03760J.].
View Article and Find Full Text PDFChem Sci
December 2024
Department of Chemistry and Hylleraas Centre for Quantum Molecular Sciences, University of Oslo Oslo 0315 Norway
The preferred structures of lithium halides (LiX, with X = Cl, Br, I) in organic solvents have been the subject of a wide scientific debate, and a large variety of forms has been isolated and characterized by X-ray diffraction. The identified molecular scaffolds for LiX are diverse, often built on (LiX) rings with a prevalence of rhomboidal arrangements and an appropriate number of solvent or Lewis base molecules coordinating the lithium ions. Much less is known about the structures of LiX in solution, limiting the understanding of the synergistic role of LiX in reactions with various organometallic complexes, as prominently represented by the turbo Grignard reaction.
View Article and Find Full Text PDFACS Appl Mater Interfaces
October 2024
Centre for Cooperative Research on Alternative Energies (CIC energiGUNE), Basque Research and Technology Alliance (BRTA), 01510 Vitoria-Gasteiz, Spain.
Carbohydr Res
November 2024
Key Laboratory of Green Chemistry and Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu, Sichuan, 610064, PR China. Electronic address:
Although the xylose mutarotation and transformation have been investigated largely separately, their relationship has been rarely systematically elaborated. The effect of several factors such as xylose concentration, temperature, and salt concentration, affecting the mutarotation of xylose are discussed. Nine alkali halides (LiCl, NaCl, KCl, LiBr, NaBr, KBr, LiI, NaI, and KI) are used to test salt effects.
View Article and Find Full Text PDFChem Sci
August 2024
Department of Chemistry, Research Institute of Natural Sciences, Gyeongsang National University Jinju 52828 Korea
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