TY - JOUR
T1 - Influence of uranyl complexation on the reaction kinetics of the dodecane radical cation with used nuclear fuel extraction ligands (TBP, DEHBA, and DEHiBA)
AU - Celis Barros, Cristian
AU - Pilgrim, Corey D.
AU - Cook, Andrew R.
AU - Mezyk, Stephen P.
AU - Grimes, Travis S.
AU - Horne, Gregory P.
N1 - Funding Information:
This research has been funded by the US-DOE Assistant Secretary for NE, under the Material Recovery and Waste Form Development Campaign, DOE-Idaho Operations Office Contract DE-AC07-05ID14517 and DE-NE0008659 Nuclear Energy Universities Program (NEUP) grant. The efforts of Cook and the picosecond pulsed electron irradiation experiments performed using the BNL Accelerator Center for Energy Research LEAF facility, were supported by the US-DOE Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences under contract DE-SC0012704.
Publisher Copyright:
© the Owner Societies 2021.
PY - 2021/11/21
Y1 - 2021/11/21
N2 - Specialized extractant ligands - such as tri-butyl phosphate (TBP),N,N-di-(2-ethylhexyl)butyramide (DEHBA), andN,N-di-2-ethylhexylisobutryamide (DEHiBA) - have been developed for the recovery of uranium from used nuclear fuel by reprocessing solvent extraction technologies. These ligands must function in the presence of an intense multi-component radiation field, and thus it is critical that their radiolytic behaviour be thoroughly evaluated. This is especially true for their metal complexes, where there is negligible information on the influence of complexation on radiolytic reactivity, despite the prevalence of metal complexes in used nuclear fuel reprocessing solvent systems. Here we present a kinetic investigation into the effect of uranyl (UO22+) complexation on the reaction kinetics of the dodecane radical cation (RH˙+) with TBP, DEHBA, and DEHiBA. Complexation had negligible effect on the reaction of RH˙+with TBP, for which a second-order rate coefficient (k) of (1.3 ± 0.1) × 1010M−1s−1was measured. For DEHBA and DEHiBA, UO22+complexation afforded an increase in their respective rate coefficients:k(RH˙++ [UO2(NO3)2(DEHBA)2]) = (2.5 ± 0.1) × 1010M−1s−1andk(RH˙++ [UO2(NO3)2(DEHiBA)2]) = (1.6 ± 0.1) × 1010M−1s−1. This enhancement with complexation is indicative of an alternative RH˙+reaction pathway, which is more readily accessible for [UO2(NO3)2(DEHBA)2] as it exhibited a much larger kinetic enhancement than [UO2(NO3)2(DEHiBA)2], 2.6×vs.1.4×, respectively. Complementary quantum mechanical calculations suggests that the difference in reaction kinetic enhancement between TBP and DEHBA/DEHiBA is attributed to a combination of reaction pathway (electron/hole transfervs.proton transfer) energetics and electron density distribution, wherein attendant nitrate counter anions effectively ‘shield’ TBP from RH˙+electron transfer processes.
AB - Specialized extractant ligands - such as tri-butyl phosphate (TBP),N,N-di-(2-ethylhexyl)butyramide (DEHBA), andN,N-di-2-ethylhexylisobutryamide (DEHiBA) - have been developed for the recovery of uranium from used nuclear fuel by reprocessing solvent extraction technologies. These ligands must function in the presence of an intense multi-component radiation field, and thus it is critical that their radiolytic behaviour be thoroughly evaluated. This is especially true for their metal complexes, where there is negligible information on the influence of complexation on radiolytic reactivity, despite the prevalence of metal complexes in used nuclear fuel reprocessing solvent systems. Here we present a kinetic investigation into the effect of uranyl (UO22+) complexation on the reaction kinetics of the dodecane radical cation (RH˙+) with TBP, DEHBA, and DEHiBA. Complexation had negligible effect on the reaction of RH˙+with TBP, for which a second-order rate coefficient (k) of (1.3 ± 0.1) × 1010M−1s−1was measured. For DEHBA and DEHiBA, UO22+complexation afforded an increase in their respective rate coefficients:k(RH˙++ [UO2(NO3)2(DEHBA)2]) = (2.5 ± 0.1) × 1010M−1s−1andk(RH˙++ [UO2(NO3)2(DEHiBA)2]) = (1.6 ± 0.1) × 1010M−1s−1. This enhancement with complexation is indicative of an alternative RH˙+reaction pathway, which is more readily accessible for [UO2(NO3)2(DEHBA)2] as it exhibited a much larger kinetic enhancement than [UO2(NO3)2(DEHiBA)2], 2.6×vs.1.4×, respectively. Complementary quantum mechanical calculations suggests that the difference in reaction kinetic enhancement between TBP and DEHBA/DEHiBA is attributed to a combination of reaction pathway (electron/hole transfervs.proton transfer) energetics and electron density distribution, wherein attendant nitrate counter anions effectively ‘shield’ TBP from RH˙+electron transfer processes.
UR - https://www.scopus.com/pages/publications/85118998289
UR - https://www.mendeley.com/catalogue/67652015-18fb-31cf-8db6-661c47169b46/
U2 - 10.1039/d1cp03797h
DO - 10.1039/d1cp03797h
M3 - Article
AN - SCOPUS:85118998289
SN - 1463-9076
VL - 23
SP - 24589
EP - 24597
JO - Physical Chemistry Chemical Physics
JF - Physical Chemistry Chemical Physics
IS - 43
ER -