4.6 Article

Gamma radiolytic stability of the novel modified diglycolamide 2,2′-oxybis(N,N-didecylpropanamide) (mTDDGA) for grouped actinide extraction

Journal

RSC ADVANCES
Volume 12, Issue 20, Pages 12416-12426

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ra08761d

Keywords

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Funding

  1. SCK CEN Academy
  2. ENEN + project from the Euratom research and training Work Programme 2016-2017 - 1 [755576]
  3. H2020 Euratom Research and Innovation Programme [755171]
  4. Excellence Initiative of the German federal government
  5. Excellence Initiative of the German state government
  6. Julich Aachen Research Alliance - High-Performance Computing
  7. JARA-CDS [jara0037, JIEK61]

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Reprocessing of spent nuclear fuel aims to improve resource efficiency and reduce radiotoxicity and heat production. The stability of a new ligand under ionizing radiation conditions was studied, and its degradation rate was found to be lower.
Reprocessing of spent nuclear fuel aims at improving resource efficiency and reducing its radiotoxicity and heat production in the long term. The necessary separation of certain metal ions from the spent fuel solutions can be achieved using different solvent extraction processes. For the scenario of the EURO-GANEX process, the use of the new, modified diglycolamide 2,2 '-oxybis(N,N-didecylpropanamide) (mTDDGA) was recently proposed to simplify the current solvent composition and reduce extraction of fission products. Before further developing the process based on this new ligand, its stability under ionizing radiation conditions needs to be studied. For this reason, gamma irradiation experiments were conducted followed by analyses with high performance liquid chromatography coupled to a mass spectrometer (HPLC-MS). The determined degradation rate of mTDDGA was found to be lower than that of the reference molecule N,N,N ',N '-tetra-n-octyl-diglycolamide (TODGA). Many identified degradation compounds of both molecules are analogues showing the same bond breaking, although also unreported de-methylation, double/triple de-alkylation and n-dodecane addition products were observed.

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