001     909859
005     20240708133759.0
037 _ _ |a FZJ-2022-03472
041 _ _ |a English
100 1 _ |a Diaz Gomez, Laura Johana
|0 P:(DE-Juel1)190476
|b 0
|e Corresponding author
|u fzj
111 2 _ |a Actinides Revisited (AnRev) 2022
|g AnRev 2022
|c Dresden
|d 2022-09-21 - 2022-09-23
|w Germany
245 _ _ |a Solvent extraction studies of different diastereomers of modified diglycolamide ligands for An(III) and Ln(III) extraction
260 _ _ |c 2022
336 7 _ |a Conference Paper
|0 33
|2 EndNote
336 7 _ |a INPROCEEDINGS
|2 BibTeX
336 7 _ |a conferenceObject
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336 7 _ |a CONFERENCE_POSTER
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336 7 _ |a Output Types/Conference Poster
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520 _ _ |a Solvent extraction is currently the preferred technique for the separation of actinides (An) from fission products(FP), and especially lanthanides (Ln), as constituents of Spent Nuclear Fuel (SNF) or PUREX raffinate. A specialinterest is on the separation of Am from Cm, Ln and other FP by testing various ligands to upgrade the currentmethods. Diglycolamide (DGA) derivatives have shown promising results as extractants for trivalent Ln and An,such as, N,N,N’,N’-tetra-n-octyl diglycolamide (TODGA), which usually have a higher affinity for Cm(III) overAm(III). Wilden et al. [1] reported a change on Am(III) selectivity over Cm(III) with methyl substitutions withdifferent orientation in the backbone of Me2-TODGA. Here, we study the selectivity and affinity of relatedextractants (TODGA and N,N,N’,N’-tetra-n-decyl diglycolamide, TDDGA) with dipropyl and ethyl-methylsubstitutions in the molecule backbone, and their respective diastereomers (syn or anti) in n-dodecane. Thechemical structures are shown in Figure 1 An inverse selectivity is observed for Am(III) over Cm(III) and otherLn(III) at high nitric acid concentration (7 - 10 mol L-1 HNO3). The steric hindrance gives low distribution ratios(D < 1.5) for the trivalent metal ions at 0.1 mol L-1 ligand concentration, as shown in Figure 2. Besides trivalentions, Pu(IV) was also tested with the interest on the complexation behavior with tetravalent ions, which showsremarkably higher distribution ratios at the same HNO3 concentrations (D > 10). This is unlike methyl anddimethyl-TODGA, which present similar distribution ratios between trivalent and tetravalent metal ions. The synethyl-methyl substitutions for both analogues showed the highest D values for Am(III) among the tested ligands,giving a promising molecule for further studies. The results of the extraction studies will be presented anddiscussed in the poster.References1. Wilden, A., et al., Unprecedented Inversion of Selectivity and Extraordinary Difference in theComplexation of Trivalent f-Elements by Diastereomers of a Methylated Diglycolamide. Chem. Eur. J.,2019. 25(21): p. 5507-5513.
536 _ _ |a 1412 - Predisposal (POF4-141)
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536 _ _ |a Verbundprojekt: Untersuchungen zur SEParation von AMericium aus hochradioaktiven Abfalllösungen (SEPAM), Teilprojekt A (02E11921A)
|0 G:(BMWi)02E11921A
|c 02E11921A
|x 1
700 1 _ |a Wilden, Andreas
|0 P:(DE-Juel1)130438
|b 1
|u fzj
700 1 _ |a Modolo, Giuseppe
|0 P:(DE-Juel1)130383
|b 2
|u fzj
700 1 _ |a Gullo, M. C.
|0 P:(DE-HGF)0
|b 3
700 1 _ |a Verboom, Willem
|0 P:(DE-HGF)0
|b 4
909 C O |o oai:juser.fz-juelich.de:909859
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910 1 _ |a Forschungszentrum Jülich
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913 1 _ |a DE-HGF
|b Forschungsbereich Energie
|l Nukleare Entsorgung, Sicherheit und Strahlenforschung (NUSAFE II)
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914 1 _ |y 2022
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980 _ _ |a poster
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