Unraveling the coordination approach of Eu(iii) in cyphos nitrate ionic liquid – a comprehensive luminescence spectroscopy study

离子液体 化学 氯化物 萃取(化学) 发光 无机化学 水溶液 硝酸盐 相(物质) 物理化学 色谱法 有机化学 材料科学 催化作用 光电子学
作者
Alok Rout,Satendra Kumar,N. Ramanathan
出处
期刊:Dalton Transactions [Royal Society of Chemistry]
卷期号:51 (14): 5534-5545 被引量:9
标识
DOI:10.1039/d2dt00422d
摘要

In consideration of the mounting attention drawn by the ionic liquid cyphos 101 (trihexyl(tetradecyl)phosphonium chloride: [P66614][Cl]) in the recovery of rare earth metals and other valuable species from their waste matrices, an effort was made using luminescence spectroscopy to study the detailed liquid-liquid extraction and coordination behavior of Eu(III) using the nitrate form of cyphos 101 (cyphos nitrate: [P66614][NO3]) in its undiluted form. Eu(III) complexation with [P66614][NO3] at each stage of the extraction process was investigated using the luminescence spectroscopy technique. Various extraction parameters such as aqueous phase acidity, concentrations of ionic liquid extractant and initial Eu(III) ion, extraction time, experimental temperature, etc. were tuned to discover their impact on the complexation process. The uniqueness of the nitrate ion in ionic liquid was explored by comparing the emission patterns of Eu(III) with [P66614]-based ionic liquids containing different anions. In addition, the affirmative effect of increasing the initial aqueous phase nitrate ion concentration in the coordination process was underscored by comparing the emission patterns in the chloride medium. The luminescence results of the Eu(III)- [P66614][NO3] complex were compared both in unirradiated and irradiated ionic liquid phases. Asymmetry ratio (AR) and lifetime data under each experimental condition were ascertained, thereby revealing the precise nature of complex formation and strength of the metal-solvate species (metal-ligand complex formation) formed. The stripping of the loaded Eu(III) from the [P66614][NO3] phase was established and the results were presented in the form of the emission patterns of Eu(III) in both phases.
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