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Abstract
The extraction of trivalent lanthanides from an aqueous phase containing 1 M NaClO4 into the room temperature ionic liquid 1-butyl-3-methylimidazolium nonafluoro-1-butanesulfonate by the β-diketone extractant 2-thenoyltrifluoroacetone (Htta) was studied. Radiotracer distribution, absorption spectroscopy, time-resolved laser-induced fluorescence spectroscopy, and X-ray absorption fine structure measurements point to the extraction of multiple lanthanide species. At low extractant concentrations, fully hydrated aqua cations of the lanthanides are present in the ionic liquid phase. As the extractant concentration is increased 1:2 and 1:3 lanthanide:tta species are observed. In contrast, 1:4 Ln:tta complexes were observed in the extraction of lanthanides by Htta into 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide.
ACKNOWLEDGEMENTS
L. TenKate and S. Naik performed the Karl-Fischer titrations. The ANL Actinide Facility for Synchrotron Radiation Research and the XOR-BESSRC staff of the APS provided infrastructure and support for the EXAFS measurements. This work, including the use of the Advanced Photon Source, was supported by the U.S. Department of Energy, Office of Basic Energy Science under contract number DE-AC02-06CH11357.
The submitted manuscript has been created by UChicago Argonne, LLC, Operator of Argonne National Laboratory (“Argonne”). Argonne, a U.S. Department of Energy Office of Science laboratory, is operated under Contract No. DE-AC02-06CH11357. The U.S. Government retains for itself, and others acting on its behalf, a paid-up nonexclusive, irrevocable worldwide license in said article to reproduce, prepare derivative works, distribute copies to the public, and perform publicly and display publicly, by or on behalf of the Government.
Notes
a Estimated absolute uncertainty ±0.5 H2O.
