The unique physicochemical properties of room-temperature ionic liquids (RTILs) have led to intense interest in these materials as alternatives to conventional organic solvents in a range of synthetic, catalytic, and electrochemical applications. Recently, there has been growing interest in their potential use in various separation processes, among them the liquid-liquid extraction of metal ions. Although certain RTIL-extractant combinations (e.g., crown ethers in 1-alkyl-3-methylimidazolium bis[(trifluoromethylsulfonyl] imides) have been shown to provide extraction efficiencies far exceeding those observed with conventional solvents, recent work suggests that the utility of RTILs may be limited by solubilization losses and difficulties in recovering extracted metal ions. In this work, we demonstrate that these limitations arise, in part, from differences in the mechanism of metal ion partitioning in RTIL systems versus conventional organic diluents and consider approaches by which they might be overcome.
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