A novel trialkyl phosphate – Ionic liquid mixture for an efficient separation of Lithium ion from its acidic feed solution

被引:0
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作者
Rout, Alok [1 ]
Palai, Manisankar. [1 ]
Ramanathan, N. [1 ,2 ]
机构
[1] Materials Chemistry & Metal Fuel Cycle Group, Indira Gandhi Centre for Atomic Research, Kalpakkam,603 102, India
[2] Indira Gandhi Centre for Atomic Research, a CI of Homi Bhabha National Institute, Kalpakkam,603102, India
关键词
Alkynes - Ligands - Solvent extraction;
D O I
10.1016/j.molliq.2024.126205
中图分类号
学科分类号
摘要
Separation of Lithium ion (Li+) using conventional non-crown type ligands through solvent extraction process is a challenging task and can only be feasible by tuning the organic phase with an additional polar environment. In this context, we have projected an extracting system containing a traditional trialkyl phosphate (T(alk)P): Tri-iso-amyl phosphate (TiAP) containing a minimal amount of ionic liquid (IL): [C4mpip][NTf2] (1-butyl-1-methylpiperidinium bis(trifluoromethanesulfonyl)imide) for the efficient extraction and separation of Li+ from its hydrochloric acid feed. The extraction performances pertaining various experimental parameters were realized to explore the solvent potentiality of TiAP/[C4mpip][NTf2] towards Li+ coordination. Involvement of two ligand molecules in extraction in presence of 10 % (v/v) IL diluent offers fast extraction kinetics and turns the extraction mechanism into a cation exchange pathway, which was further examined by using different classes of ILs in conjunction with TiAP for Li+ uptake. The selectivity of Li+ over other alkali (or alkaline earth) metal ions was investigated to highlight the affinity of the proposed IL system towards Li+. Extraction scenario in TiAP phase was compared with that in TBP phase containing same IL to bring out the efficacy of the proposed IL system. The stripping performance of Li+ from the loaded organic phase was studied using an acid solution to establish the sustainability of the proposed extraction process. © 2024 Elsevier B.V.
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