Direct Extraction of Uranium Oxides with <i>N,N</i>-Di(2-ethylhexyl)isobutyramide

The direct extraction of uranium from voloxidized nuclear fuel into an organic solvent offers several potential advantages over conventional hydrometallurgical reprocessing, including reducing the reprocessing plant footprint, providing an initial degree of decontamination from fission products, and minimizing the amount of secondary waste from nitric acid. In this work, the direct extraction of uranium oxides into 1.5 M <i>N,N</i>-di(2-ethylhexyl)isobutyramide (DEHiBA) in <i>n-</i>dodecane is examined. UV-vis spectra and distribution ratios of HNO<sub>2</sub> in 1.5 M DEHiBA as well as the equilibrium organic phase H<sub>2</sub>O concentrations in HNO<sub>3</sub>-loaded 1.5 M DEHiBA are also reported. Hypothesized reaction stoichiometries for the direct extraction of uranium from UO<sub>2</sub>, α-U<sub>3</sub>O<sub>8</sub>, and ε-UO<sub>3</sub> are verified through analysis of organic-phase U, HNO<sub>2</sub>, and HNO<sub>3</sub> concentrations after dissolution. Water generated by the dissolution results in the formation of a separate aqueous phase, which will need to be accounted for in future flowsheet design.

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Publication Details

Journal
ACS Omega
Published
2025-03-28
DOI
https://doi.org/10.1021/acsomega.5c01103
Primary Topic
Radioactive element chemistry and processing
Type
article
Field-Weighted Citation Impact
0.00

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article

Direct Extraction of Uranium Oxides with N,N-Di(2-ethylhexyl)isobutyramide

Amy L. Speelman, Ashley Williams, Gabriel B. Hall, Gregg J. Lumetta et al.
ACS Omega
Radioactive element chemistry and processing
article

Direct Extraction of Uranium Oxides with N,N-Di(2-ethylhexyl)isobutyramide

Amy L. Speelman, Ashley Williams, Gabriel B. Hall, Gregg J. Lumetta, Bruce K. McNamara, Nathan P. Bessen, Daria Boglaienko, Sergey I. Sinkov, Avalon B. Tarbet-Mendoza
article en

Abstract

The direct extraction of uranium from voloxidized nuclear fuel into an organic solvent offers several potential advantages over conventional hydrometallurgical reprocessing, including reducing the reprocessing plant footprint, providing an initial degree of decontamination from fission products, and minimizing the amount of secondary waste from nitric acid. In this work, the direct extraction of uranium oxides into 1.5 M <i>N,N</i>-di(2-ethylhexyl)isobutyramide (DEHiBA) in <i>n-</i>dodecane is examined. UV-vis spectra and distribution ratios of HNO<sub>2</sub> in 1.5 M DEHiBA as well as the equilibrium organic phase H<sub>2</sub>O concentrations in HNO<sub>3</sub>-loaded 1.5 M DEHiBA are also reported. Hypothesized reaction stoichiometries for the direct extraction of uranium from UO<sub>2</sub>, α-U<sub>3</sub>O<sub>8</sub>, and ε-UO<sub>3</sub> are verified through analysis of organic-phase U, HNO<sub>2</sub>, and HNO<sub>3</sub> concentrations after dissolution. Water generated by the dissolution results in the formation of a separate aqueous phase, which will need to be accounted for in future flowsheet design.

ACS OmegaVol. 10(13)
Pacific Northwest National Laboratory (US)
Nuclear Fuel Cycle and Supply Chain
Openalex Percentile: Top 95%
Radioactive element chemistry and processing
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