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TBP-P507
SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

Polymer microcapsules containing TBP–P507 prepared through in situ cross-linking for highly stable and selective extraction of Li+ from high-Mg2+/Li+-ratio brines

Chao Zhang,Tian Xie,Han Qu,Guofei Li,Zhongyu Zhao,Wanji Zhou,Shiai Xu,Zheng Li

The efficient separation and extraction of Li + from salt lake brines with a high Mg 2+ /Li + ratio remains challenging. Herein, poly(vinyl alcohol-co-ethylene) microcapsules encapsulating tributyl phosphate (TBP) and mono-2-ethylhexyl 2-ethylhexyl phosphate (P507) as carriers were successfully fabricated via one-step phase inversion followed by in situ cross-linking with boric acid. Correspondingly, the obtnined microcapsules possess a fine three-dimensional cross-linked network structure, which can effectively stabilize the extractant carriers and significantly enhance the encapsulation stability. These microcapsules were employed for the stable and selective extraction of Li + from high-Mg 2+ /Li + -ratio brines. The surface morphology, composition, structure, and adsorption characteristics of the TBP–P507 microcapsules were thoroughly investigated. The microcapsules comprising 30 wt% (m/m) polymer matrix and 70 wt% (m/m) TBP–P507 as the extractant (denoted as TBP–P507/P-3) exhibited the highest separation efficiency for Li + and Mg 2+ . The separation factor of Li + over Mg 2+ was up to 427, and the equilibrium adsorption capacity of the TBP–P507/P-3 microcapsules for Li + reached 0.83 mg/g in synthetic brine with a low Li + concentration and a high Mg 2+ /Li + ratio. These results illustrated that Li + could be separated with high selectivity over Mg 2+ . Adsorption kinetics and isotherms investigations indicated that Li + adsorption by TBP–P507/P-3 conformed to the pseudo-second-order kinetic model and was consistent with the Langmuir–Freundlich model, with the mechanism classified as chemisorption. Accordingly, the maximum amount of Li + adsorbed by the TBP–P507/P-3 microcapsules calculated using the Langmuir–Freundlich model was 4.4 mg/g. After 10 adsorption–elution cycles with pure water as the eluent, 96 % of the maximum equilibrium adsorption capacity was retained. The results clearly illustrate the construction of a finely-tuned three-dimensional cross-linked network structure is pivotal to enhancing stability of the microcapsules, efficiently decreasing the risk of carrier leakage from the involved polymer matrixes. Overall, this research presents a valuable microcapsule technology for separating and extracting Li + from high-Mg 2+ /Li + -ratio salt lake brines.

CAS / MDL: 9002-86-2 25067-34-9
研究领域: 材料科学 · 环境科学 · 化学工程
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JOURNAL OF SOLID STATE CHEMISTRY · 2025 · IF 3.5

Developing a green lithium extraction process: insights into the TBP - P507 system and its industrial potential

Huifang Li,Shuo Wang,Wenbin Fan,Dahuan Liu

Solvent extraction has emerged as a highly promising method for lithium extraction . In this study, a sustainable extraction system was developed using 2-ethylhexyl phosphate mono 2-ethylhexyl ester (P507) and tri-butyl phosphate (TBP). By precisely controlling the coordination mode of Fe 3+ with TBP and P507 during the stripping process, a green extraction process was achieved. The research comprehensively investigated the effects of various factors, such as the type of diluent, saponification ratio, volume ratio of TBP, molar ratio of Fe/Li, and extraction phase ratio. Through systematic experiments, the optimal parameters were identified, and the coordination mechanism between the organic compounds and metal ions was elucidated. This work not only provides a promising approach for lithium recovery from salt lake brines but also establishes a solid theoretical foundation for the industrial application of the TBP-P507 extraction system, thereby holding great potential for promoting the development of the lithium extraction industry.

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