Testing Low-Density Polyethylene Membranes for Lithium Isotope Electromigration System

The growing energy demand has emphasized the importance of developing nuclear technologies and high-purity lithium isotopes (<sup>6</sup>Li and <sup>7</sup>Li) as raw materials. This study investigates how voltage and migration time affect two types of low-density polyethylene membranes-one impregnated with ionic liquids and the other non-impregnated-for lithium isotope separation via electromigration from a lithium-loaded organic phase to an aqueous solution. We developed a laboratory-made setup for high-precision lithium isotope measurements (2RSD = ±0.30‱) of natural carbonate samples (LSVEC) and an optimized protocol for isotope ratio measurements using quadrupole ICP-MS with the sample-standard bracketing method (SSB). The results document that both impregnated and non-impregnated membranes can achieve promising <sup>6</sup>Li enrichment under different environmental conditions, including ionic liquids and organic solutions in the cathode chamber. Lithium-ion mobility is influenced by voltage in an environment assisted by 0.1 mol/L tetrabutylammonium perchlorate and increases quasi-linearly from 5 to 15 V. Between 20 and 25 h, the lithium-ion concentration had the maximum value, after which the trend declined. In the BayesGLM model, we incorporated all data and systematically eliminated those with a low enrichment factor, either individually or in groups. Our findings indicated that the model was not significantly affected by the exclusion of measurements with low α. This suggests that voltage and migration time are crucial, and achieving a better enrichment factor depends on applying the optimal ratio of ionic liquids, crown ethers, and organic solvents. Ionic liquids used for impregnation sustain enrichment in the first hours, particularly for <sup>7</sup>Li; however, after 25 h, <sup>6</sup>Li demonstrated a higher enrichment capacity. The maximum single-stage separation factor for <sup>6</sup>Li/<sup>7</sup>Li was achieved at 24 and 48 h for an impregnated membrane M2 (α = 1.021/1.029) and a non-impregnated membrane M5 (α = 1.031/1.038).

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Journal
Materials
Published
2025-05-27
DOI
https://doi.org/10.3390/ma18112519
Primary Topic
Extraction and Separation Processes
Type
article
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article

Testing Low-Density Polyethylene Membranes for Lithium Isotope Electromigration System

Ana-Maria Nasture, Ramona Zgavarogea, Roxana Elena Ionete, Constantin Nechita et al.
Materials
Extraction and Separation Processes
article

Testing Low-Density Polyethylene Membranes for Lithium Isotope Electromigration System

Ana-Maria Nasture, Ramona Zgavarogea, Roxana Elena Ionete, Constantin Nechita, Andreea Maria Iordache, Rui Santos, Erdin Feizula
article en

Abstract

The growing energy demand has emphasized the importance of developing nuclear technologies and high-purity lithium isotopes (<sup>6</sup>Li and <sup>7</sup>Li) as raw materials. This study investigates how voltage and migration time affect two types of low-density polyethylene membranes-one impregnated with ionic liquids and the other non-impregnated-for lithium isotope separation via electromigration from a lithium-loaded organic phase to an aqueous solution. We developed a laboratory-made setup for high-precision lithium isotope measurements (2RSD = ±0.30‱) of natural carbonate samples (LSVEC) and an optimized protocol for isotope ratio measurements using quadrupole ICP-MS with the sample-standard bracketing method (SSB). The results document that both impregnated and non-impregnated membranes can achieve promising <sup>6</sup>Li enrichment under different environmental conditions, including ionic liquids and organic solutions in the cathode chamber. Lithium-ion mobility is influenced by voltage in an environment assisted by 0.1 mol/L tetrabutylammonium perchlorate and increases quasi-linearly from 5 to 15 V. Between 20 and 25 h, the lithium-ion concentration had the maximum value, after which the trend declined. In the BayesGLM model, we incorporated all data and systematically eliminated those with a low enrichment factor, either individually or in groups. Our findings indicated that the model was not significantly affected by the exclusion of measurements with low α. This suggests that voltage and migration time are crucial, and achieving a better enrichment factor depends on applying the optimal ratio of ionic liquids, crown ethers, and organic solvents. Ionic liquids used for impregnation sustain enrichment in the first hours, particularly for <sup>7</sup>Li; however, after 25 h, <sup>6</sup>Li demonstrated a higher enrichment capacity. The maximum single-stage separation factor for <sup>6</sup>Li/<sup>7</sup>Li was achieved at 24 and 48 h for an impregnated membrane M2 (α = 1.021/1.029) and a non-impregnated membrane M5 (α = 1.031/1.038).

MaterialsVol. 18(11)
Universidade do Porto (PT), National Institute for Research and Development in Forestry "Marin Drăcea" (RO), National Institute for Research and Development of Isotopic and Molecular Technologies (RO)
Openalex Percentile: Top 89%
Extraction and Separation Processes
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