化学
三辛基氧化膦
稀释剂
萃取(化学)
共晶体系
无机化学
溶解度
离子液体
锂(药物)
分离过程
碱金属
溶剂化
相图
选择性
超临界流体
COSMO-RS公司
溶剂
氢键
分析化学(期刊)
深共晶溶剂
硝酸锂
液-液萃取
密度泛函理论
相(物质)
溶解
摩尔浓度
作者
Xiang Wei,Shigao Shen,Yuhang Fan,Qian Liu,Zhen Song,Hongye Cheng,Zhiwen Qi
标识
DOI:10.1021/acs.jced.5c00702
摘要
As alkali metals have similar physicochemical properties, efficient separation of lithium and sodium is a common challenge in the fields of salt lake brine processing and lithium battery resource recycling. In this work, a hydrophobic deep eutectic solvent (HDES) composed of dibenzoylmethane (DBM) and trioctylphosphine oxide (TOPO) was investigated for the selective extraction of lithium ions. The solid–liquid equilibrium phase diagram confirmed eutectic formation. By adjusting the molar ratio of DBM-TOPO, the solubility of the HDES in the diluent and its lithium ion extraction performance were enhanced, ultimately yielding a single-stage Li+ extraction efficiency of 91.1% and a Li+/Na+ separation selectivity of 92.6. Density and viscosity were measured across a temperature range and correlated using a linear equation and the Vogel–Fulcher–Tammann equation, respectively. Spectroscopic analyses (FT-IR, 1H NMR) and density functional theory (DFT) calculations demonstrated that hydrogen bonding between enol-form DBM and TOPO drives HDES formation and preferential coordination with Li+. These findings provide both experimental data and molecular-level understanding of DBM-TOPO HDESs, supporting their application in high-performance lithium extraction systems.
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