A Novel Mechanism for the Extraction of Metals from Water to Ionic Liquids

被引:27
作者
Janssen, Camiel H. C. [3 ,4 ]
Sanchez, Antonio [1 ]
Witkamp, Geert-Jan [3 ]
Kobrak, Mark N. [1 ,2 ]
机构
[1] CUNY Brooklyn Coll, Dept Chem, Brooklyn, NY 11210 USA
[2] CUNY, Dept Chem, Grad Ctr, New York, NY 10016 USA
[3] Delft Univ Technol, Fac Sci Appl, Dept Biotechnol, NL-2628 BC Delft, Netherlands
[4] Wetsus Ctr Excellence Sustainable Water Technol, NL-8900 CC Leeuwarden, Netherlands
关键词
crown compounds; ion chromatography; ion exchange; ionic liquids; thermodynamics; STRUCTURAL VARIATIONS; SOLVENT-EXTRACTION; AQUEOUS-SOLUTIONS; CROWN-ETHERS; COORDINATION; GREENNESS; EXCHANGE;
D O I
10.1002/cphc.201300686
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We present a novel mechanism for the extraction of metals from aqueous phases to room-temperature ionic liquids (ILs) by use of a high-temperature salt as an extraction agent. The mechanism capitalizes on the fact that charged metal complexes are soluble in ILs; this allows for extraction of charged complexes rather than the neutral species, which are formed by conventional approaches. The use of a well-chosen extraction agent also suppresses the competing ion-exchange mechanism, thus preventing degradation of the ionic liquid. The approach permits the use of excess extractant to drive the recovery of metals in high yield. This work presents both a thermodynamic framework for understanding the approach and experimental verification of the process in a range of different ILs. The method has great potential value in the recovery of metals, water purification and nuclear materials processing.
引用
收藏
页码:3806 / 3813
页数:8
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