Issue 15, 2024

Electromigration separation of lithium isotopes with B12C4, B15C5 and B18C6 systems

Abstract

High abundance 6Li and 7Li are essential materials for the nuclear industry. In this article, the lithium isotope separation effect and lithium-ion transport of a “lithium salt aqueous solution (anolyte)|crown ethers–ionic liquid organic solution|ammonium chloride aqueous solution (catholyte)” electromigration system with B12C4, B15C5 and B18C6 as phase transfer catalysts were investigated systematically. The results show that separation factors can reach 1.028 (B12C4), 1.024 (B15C5) and 1.011 (B18C6), respectively, when LiCl solution is used as the anolyte. The separation effect mainly originated from interfaces between anolytes and organic solutions, and was less affected by an electric field. The separation effect between organic solution and catholytes was greatly affected by the electric field for B12C4 and B15C5 systems, which converted from 7Li-enrichment to 6Li-enrichment with increased voltage. For the B18C6 system it was less affected. Furthermore, lithium ion transport in B12C4, B15C5 and B18C6 systems was greatly promoted by the electric field, with the Li+ concentration in catholytes of B12C4, B15C5 and B18C6 systems increased from 0.088 mg L−1, 0.286 mg L−1 and 0.778 mg L−1 to 8.321 mg L−1, 7.422 mg L−1 and 4.631 mg L−1 respectively as the voltage increased from 2 V to 16 V. The B12C4 system has been confirmed as the optimal solution considering both the Li+ transport and isotope separation effect.

Graphical abstract: Electromigration separation of lithium isotopes with B12C4, B15C5 and B18C6 systems

Supplementary files

Article information

Article type
Paper
Submitted
28 Dec 2023
Accepted
10 Mar 2024
First published
12 Mar 2024

New J. Chem., 2024,48, 6676-6687

Electromigration separation of lithium isotopes with B12C4, B15C5 and B18C6 systems

Z. Zhao, X. Zhou, Q. Meng, P. Zhang, F. Shao, X. Li, H. Li, L. Mao, T. Zheng, Y. Jing, Y. Jia, S. Wang and J. Sun, New J. Chem., 2024, 48, 6676 DOI: 10.1039/D3NJ05963D

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