Selective Solid-Liquid Extraction of Lithium Cation Using Tripodal Sulfate-Binding Receptors Driven by Electrostatic Interactions.

Molecules

Key Laboratory of Medicinal Molecule Science and Pharmaceutics Engineering, Ministry of Industry and Information Technology, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 102488, China.

Published: May 2024

AI Article Synopsis

  • * Researchers developed tripodal hexaurea anion receptors that can effectively extract lithium sulfate into a water-DMSO solution, demonstrating a significant selectivity for lithium over other alkali metals like sodium and potassium.
  • * The selective extraction process relies on electrostatic interactions and ion-dipole interactions that depend on the size of the cation, providing valuable insights for designing better receptors for ion separation.

Article Abstract

Owing to the important role of and increasing demand for lithium resources, lithium extraction is crucial. The use of molecular extractants is a promising strategy for selective lithium recovery, in which the interaction between lithium and the designed extractant can be manipulated at the molecular level. Herein, we demonstrate that anion receptors of tripodal hexaureas can selectively extract LiSO solids into water containing DMSO (0.8% water) compared to other alkali metal sulfates. The hexaurea receptor with terminal hexyl chains displays the best Li extraction selectivity at 2-fold over Na and 12.5-fold over K. The driving force underpinning selective lithium extraction is due to the combined interactions of Li-SO electrostatics and the ion-dipole interaction of the lithium-receptor (carbonyl groups and N atoms); the latter was found to be cation size dependent, as supported by computational calculations. This work indicates that anion binding receptors could drive selective cation extraction, thus providing new insights into the design of receptors for ion recognition and separation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11173669PMC
http://dx.doi.org/10.3390/molecules29112445DOI Listing

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