4.6 Article

Characterization of a Ternary Neodymium-HEDTA-Citrate Complex in the Actinide Lanthanide Separation Process

Journal

ACS OMEGA
Volume 7, Issue 17, Pages 15005-15015

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.2c00759

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Funding

  1. Department of Energy Office of Nuclear Energy [DE-NE0008554]

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The actinide lanthanide separation (ALSEP) process is a method used to separate americium and curium from lanthanide fission products, reducing the radioactivity and heat loading of nuclear waste. This process utilizes HEDTA as the primary ligand to selectively strip the actinides while leaving the lanthanides behind. A new ternary lanthanide-HEDTA-citrate complex was discovered during experiments.
The actinide lanthanide separation (ALSEP) process is a modern solvent extraction approach used for the separation of the minor actinides americium and curium from the lanthanide fission products for transmutation, a process that can significantly reduce the long-term radioactivity and heat loading of nuclear waste. This process, inspired by existing chemistry, uses the aminopolycarboxylate N-(2-hydroxyethyl)ethylenediamineN,N',N'-triacetic acid (HEDTA) to selectively separate the actinides by stripping them from the organic phase while leaving the lanthanides behind. HEDTA is used in this separation as it has been shown to exhibit faster extraction kinetics than other aminopolycarboxylates, but its lower coordination number can allow for the formation of higher order complexes with the typically 8- to 9-coordinate f-elements. ALSEP uses a carboxylic add buffer in the aqueous phase to control the pH of the system during metal stripping, and this buffer has the ability to complex actinide(III) and lanthanide(III) ions. The presence of a previously uncharacterized ternary lanthanide-HEDTA-citrate complex was detected during single-phase spectroscopy experiments. A combination of partitioning experiments and spectrophotometric titration led to the identification of a 1:1:1 complex containing a partially protonated citrate ligand and determination of the stability constant of its neodymium complex.

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