Sorption of Strontium to Uraninite and Uranium(IV)-Silicate Nanoparticles.

Langmuir

Research Centre for Radwaste Disposal and Williamson Research Centre, School of Earth & Environmental Sciences, The University of Manchester, Oxford Road, Manchester M13 9PL, U.K.

Published: March 2022

AI Article Synopsis

  • Spent nuclear fuel contains uranium and strontium-90, a key radioactive contaminant, and their interactions are not well understood.
  • The study investigates strontium's sorption behavior with two relevant uranium phases across a pH range of 4-14, finding that strontium shows the strongest affinity for UO, especially at higher pH levels.
  • Advanced techniques like EXAFS spectroscopy reveal that strontium interacts with uranium in complex ways, significantly influencing its mobility in nuclear fuel storage environments.

Article Abstract

Spent nuclear fuel contains both uranium (U) and high yield fission products, including strontium-90 (Sr), a key radioactive contaminant at nuclear facilities. Both U and Sr will be present where spent nuclear fuel has been processed, including in storage ponds and tanks. However, the interactions between Sr and U phases under ambient conditions are not well understood. Over a pH range of 4-14, we investigate Sr sorption behavior in contact with two nuclear fuel cycle relevant U(IV) phases: nano-uraninite (UO) and U(IV)-silicate nanoparticles. Nano-UO is a product of the anaerobic corrosion of metallic uranium fuel, and UO is also the predominant form of U in ceramic fuels. U(IV)-silicates form stable colloids under the neutral to alkaline pH conditions highly relevant to nuclear fuel storage ponds and geodisposal scenarios. In sorption experiments, Sr had the highest affinity for UO, although significant Sr sorption also occurred to U(IV)-silicate phases at pH ≥ 6. Extended X-ray absorption fine structure (EXAFS) spectroscopy, transmission electron microscopy, and desorption data for the UO system suggested that Sr interacted with UO via a near surface, highly coordinated complex at pH ≥ 10. EXAFS measurements for the U(IV)-silicate samples showed outer-sphere Sr sorption dominated at acidic and near-neutral pH with intrinsic Sr-silicates forming at pH ≥ 12. These complex interactions of Sr with important U(IV) phases highlight a largely unrecognized control on Sr mobility in environments of relevance to spent nuclear fuel management and storage.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098169PMC
http://dx.doi.org/10.1021/acs.langmuir.1c02927DOI Listing

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