4.6 Article

Chemical characterisation of degraded nuclear fuel analogues simulating the Fukushima Daiichi nuclear accident

Journal

NPJ MATERIALS DEGRADATION
Volume 6, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41529-022-00219-3

Keywords

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Funding

  1. UK Engineering and Physical Science Research Council (EPSRC) [EP/N017374/1, EP/R01924X/1, EP/S020659/1, EP/S01019X/1]
  2. Nuclear Decommissioning Authority
  3. EPSRC
  4. BEIS [EP/T011424/151]
  5. DOE Office of Science [DESC0012704]

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The Fukushima Daiichi accident resulted in the creation of molten core-concrete interaction (MCCI) material, which is a mixture of degraded nuclear fuel material and other reactor components. Analysis of this material revealed the presence of various minerals containing U-Zr-O, as well as crystalline silicate phases and a Ce-bearing mineral called perclevite. The formation of perclevite was a result of a reaction between the U-Zr-O-depleted Ce-Nd-O melt and the silicate melt. Most of the U was found in the form of U4+, while Ce was present as Ce3+.
The Fukushima Daiichi accident generated degraded nuclear fuel material, mixed with other reactor components, known as molten core-concrete interaction (MCCI) material. Simulant MCCI material was synthesised, excluding highly radioactive fission products, containing depleted U, and incorporating Ce as a surrogate for Pu. Multi-modal mu-focus X-ray analysis revealed the presence of the expected suite of U-Zr-O containing minerals, in addition to crystalline silicate phases CaSiO3, SiO2-cristobalite and Ce-bearing percleveite, (Ce,Nd)(2)Si2O7. The formation of perclevite resulted from reaction between the U-Zr-O-depleted Ce-Nd-O melt and the silicate (SiO2) melt. It was determined that the majority of U was present as U4+, whereas Ce was observed to be present as Ce3+, consistent with the highly reducing synthesis conditions. A range of Fe-containing phases characterised by different average oxidation states were identified, and it is hypothesised that their formation induced heterogeneity in the local oxygen potential, influencing the oxidation state of Ce.

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