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Efficient lithium extraction via electrodialysis using acid-processed lithium-adsorbing lithium lanthanum titanate
Increasing demands of lithium (Li) for lithium-ion batteries (LIBs) call for efficient Li extraction methods from natural resources and used LIBs. In this study, we efficiently extract Li from a Li-containing solution via electrodialysis using a fast ion conductor, lithium lanthanum titanate (LLT, L...
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Published in: | Desalination 2022-12, Vol.543, p.116117, Article 116117 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Increasing demands of lithium (Li) for lithium-ion batteries (LIBs) call for efficient Li extraction methods from natural resources and used LIBs. In this study, we efficiently extract Li from a Li-containing solution via electrodialysis using a fast ion conductor, lithium lanthanum titanate (LLT, Li0.29La0.57TiO3), as a separation membrane. Here, the LLT surface was modified by immersing in a strong acid solution such as hydrochloric acid to adsorb Li ions. For a mixed alkaline solution of lithium hydroxide, sodium hydroxide, and potassium hydroxide with a 0.1-M concentration, the maximum extraction speed of Li reached 3.5 mg/h when 5 V voltage was applied to the ionic conductor membrane with an area of 16 cm2. With the Li-adsorbing LLT, 40 mg of Li was extracted after 72 h from an aqueous solution in which Li was eluted by immersing black powder of used LIBs in water. The result indicates that high alkalinity may play a key role to achieve fast extraction.
•Efficient lithium extraction from aqueous solution can be done with Li-adsorbing ionic conductor.•The lithium extraction demonstrates perfect selectivity of Li against Na and K.•Acid treatment of Li0.29La0.57TiO3 produces Li-adsorbing ionic conductor LA-LLT.•Extraction is faster for solutions with high alkalinity.•The method, LiSMIC, can be applied to recycling of Li from used Li-ion batteries. |
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ISSN: | 0011-9164 1873-4464 |
DOI: | 10.1016/j.desal.2022.116117 |