Selective Lithium extraction from clay minerals using a Superacidic urea–Methanesulfonic acid deep eutectic solvent

Urea–methanesulfonic acid (MSA) deep eutectic solvents (DESs) are reported here for the first time as a green, superacidic platform for the highly selective extraction of lithium (Li) from clay-bearing ores. Formulated in molar ratios from 1:2 to 1:8, these DESs were characterized using Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, 1 H and 13 C nuclear magnetic resonance (NMR), ultraviolet-visible (UV–Vis) spectroscopy, alongside density functional theory (DFT) to map their unique molecular interactions and tuneable acidity. Spectroscopic and computational analyses revealed a transition from hydrogen-bond-dominant to ionic environments as the MSA ratio increased, with DFT indicating rising interaction energies (1.583 to 3.237 eV) and vibrational signatures of protonation. The urea-MSA 1:2 system, optimized with 20% water, maintained superacidity ( H 0 = −3.102) and achieved a remarkable 100% extraction efficiency for Li, Na, and Sr. Critically, the system exhibited superior selectivity, recovering 100% Li while leaching only 23% Al and 6% K, significantly outperforming conventional sulfuric acid (4% Li) and citric acid (92% Li). This selectivity is attributed to a “coordination window” where the superacidic protons effectively disrupt the mineral lattice while the DES components inhibit the total dissolution of structural impurities. These findings demonstrate that urea-MSA DESs serve as high-performance, recyclable, and sustainable alternatives for the selective recovery of critical metals. By operating at moderate temperatures with high atom economy, this system offers a viable industrial pathway for the green valorization of complex mineral matrices, addressing the urgent need for sustainable lithium sourcing in the global energy transition. • Urea-MSA DESs formulated and characterized across 1:2 to 1:8 ratios. • FTIR, Raman, and NMR show a shift from H-bonding to an ionic environment. • Pure DESs exhibit superacidic behavior: H 0 from −3.501 to −5.681. • Achieved 100% Li, Na, and Sr extraction from complex Serbian clay-hosted ore. • High selectivity for Li over structural gangue elements like Al (23%) and K (6%). • DFT analysis links molecular reactivity descriptors to macroscopic leaching performance.

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Publication Details

Journal
Separation and Purification Technology
Published
2026-02-04
DOI
https://doi.org/10.1016/j.seppur.2026.137148
Citations
1
Primary Topic
Extraction and Separation Processes
Type
article
Field-Weighted Citation Impact
19.05
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article

Selective Lithium extraction from clay minerals using a Superacidic urea–Methanesulfonic acid deep eutectic solvent

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article

Selective Lithium extraction from clay minerals using a Superacidic urea–Methanesulfonic acid deep eutectic solvent

Ian J. Scowen, Yousef Ghorbani, Hosein Ghaedi, Payam Kalhor, Cristian Serrano Araya, Enrico Ferrari, Tasnim Munshi, Cora Dawson-Jones
article en
1 citations

Abstract

Urea–methanesulfonic acid (MSA) deep eutectic solvents (DESs) are reported here for the first time as a green, superacidic platform for the highly selective extraction of lithium (Li) from clay-bearing ores. Formulated in molar ratios from 1:2 to 1:8, these DESs were characterized using Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, 1 H and 13 C nuclear magnetic resonance (NMR), ultraviolet-visible (UV–Vis) spectroscopy, alongside density functional theory (DFT) to map their unique molecular interactions and tuneable acidity. Spectroscopic and computational analyses revealed a transition from hydrogen-bond-dominant to ionic environments as the MSA ratio increased, with DFT indicating rising interaction energies (1.583 to 3.237 eV) and vibrational signatures of protonation. The urea-MSA 1:2 system, optimized with 20% water, maintained superacidity ( H 0 = −3.102) and achieved a remarkable 100% extraction efficiency for Li, Na, and Sr. Critically, the system exhibited superior selectivity, recovering 100% Li while leaching only 23% Al and 6% K, significantly outperforming conventional sulfuric acid (4% Li) and citric acid (92% Li). This selectivity is attributed to a “coordination window” where the superacidic protons effectively disrupt the mineral lattice while the DES components inhibit the total dissolution of structural impurities. These findings demonstrate that urea-MSA DESs serve as high-performance, recyclable, and sustainable alternatives for the selective recovery of critical metals. By operating at moderate temperatures with high atom economy, this system offers a viable industrial pathway for the green valorization of complex mineral matrices, addressing the urgent need for sustainable lithium sourcing in the global energy transition. • Urea-MSA DESs formulated and characterized across 1:2 to 1:8 ratios. • FTIR, Raman, and NMR show a shift from H-bonding to an ionic environment. • Pure DESs exhibit superacidic behavior: H 0 from −3.501 to −5.681. • Achieved 100% Li, Na, and Sr extraction from complex Serbian clay-hosted ore. • High selectivity for Li over structural gangue elements like Al (23%) and K (6%). • DFT analysis links molecular reactivity descriptors to macroscopic leaching performance.

Separation and Purification TechnologyVol. 391
University of Southampton (GB), University of Lincoln (GB), Keele University (GB)
Responsible consumption and production
Openalex Percentile: Top 2%
Extraction and Separation Processes
19.05
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