RESUMEN
In this work, we studied the extraction systems for the separation f-elements based on the tetradentate N,O-donor ligand di(N-ethyl-4-ethylanilide) 2,2'-dipyridyl-6,6'-dicarboxylic acid (L). The organic phase of these systems was perspective fluorine-containing organic solvents-metanitrobenzotrifluoride (F-3), ionic liquid C4mimNTf2 (IL), and their mixture. The increase of Am(III) selectivity in the presence of Ln(III) in cases of the diluent mixture was shown. The mechanism of the f-element complexation leading to the improved properties of the extraction systems was studied by UV-visible, Raman-spectroscopy, XRD-study, and density functional theory calculations.
RESUMEN
Reprocessing of spent nuclear fuel (SNF) is an important task in a frame of ecology and rational use of natural resources. Uranium, as the main component of SNF (>95%), can be recovered for further use as fresh nuclear fuel. To minimize an amount of solid radioactive waste generated during SNF reprocessing, new extractants are under investigation. Diamides of 1,10-phenanthroline-2,9-dicarboxylic acid are perspective tetradentate N-donor ligands that form strong complexes with f-elements, which are soluble in polar organic solvents. As an example of three ligands of this class, we conducted a comparative study and showed how the substituent in the amide functional group affects the extraction ability toward uranyl nitrate from nitric acid media. We have performed a careful study (NMR, FT-IR, XRD, RMC-EXAFS) of the structures of synthesized complexes of new ligands with uranyl nitrate and used quantum mechanical calculations to explain the discovered regularities through.