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在含杯芳烃的室温离子液体中银离子的溶剂萃取与反萃取

Solvent extraction and stripping of silver ions in room-temperature ionic liquids containing calixarenes.

作者信息

Shimojo Kojiro, Goto Masahiro

机构信息

Department of Applied Chemistry, Graduate School of Engineering, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka, 812-8581, Japan.

出版信息

Anal Chem. 2004 Sep 1;76(17):5039-44. doi: 10.1021/ac049549x.

Abstract

We found that a calix[4]arene-bearing pyridine is soluble in a typical room-temperature ionic liquid (RTIL), 1-alkyl-3-methylimidazolium hexafluorophosphate. Pyridinocalix[4]arene showed a high extraction ability and selectivity for silver ions. The extraction performance of the calix[4]arene was greatly enhanced by dissolution in RTILs compared to in chloroform. In a competitive extraction test using five different metal ions (Ag+, Cu2+, Zn2+, Co2+, Ni2+), only silver ions were transferred by the calix[4]arene from the aqueous feed phase into the RTILs, through a cation-exchange mechanism. The pyridinocalix[4]arene was found to form a stable 1:1 complex with silver ions, both by slope analysis and by Job's method. Since it is easy to strip silver ions from RTILs by controlling the aqueous-phase pH, the extraction performance of calix[4]arene in RTILs was maintained after five repeated uses.

摘要

我们发现,一种含杯[4]芳烃的吡啶可溶于典型的室温离子液体(RTIL),即1-烷基-3-甲基咪唑六氟磷酸盐。吡啶杯[4]芳烃对银离子表现出高萃取能力和选择性。与在氯仿中相比,杯[4]芳烃在RTILs中的溶解极大地提高了其萃取性能。在使用五种不同金属离子(Ag +、Cu2 +、Zn2 +、Co2 +、Ni2 +)的竞争性萃取试验中,杯[4]芳烃仅通过阳离子交换机制将银离子从水相进料相转移到RTILs中。通过斜率分析和乔布氏法发现,吡啶杯[4]芳烃与银离子形成稳定的1:1配合物。由于通过控制水相pH值很容易从RTILs中反萃银离子,杯[4]芳烃在RTILs中的萃取性能在五次重复使用后仍得以保持。

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