Nanoparticulate and colloidal uranium and plutonium in spent nuclear fuel storage pond effluents.

Colloids present a challenge for nuclear decommissioning and disposal due to their potential to mobilise radionuclides. Waste retrieval and decommissioning of storage ponds for spent nuclear fuel and silos for radioactive waste at the Sellafield nuclear facility, UK, are high priorities. The particulates characterised here originate from facilities > 60 years old and provide a unique opportunity to investigate the long-term fate of radionuclides in an aquatic, engineered storage environment. Radioactive effluents were obtained from a legacy pond and characterised using ultrafiltration, transmission electron microscopy (TEM) and actinide L3 edge X-ray absorption spectroscopy (XAS). TEM analysis showed discrete UO2-like nanoparticles, 5-10 nm in size, often co-associated with Mg-Al- and Fe-(oxyhydr)oxide colloidal phases. Uranium XAS indicated a mix of uranium oxidation states with EXAFS suggesting U(IV)-oxide nanoparticles and sorbed U(VI). Pu XANES identified Pu(IV) as the dominant oxidation state. Both U and Pu associates with large, Mg/Al- and Fe-(oxyhydr)oxide agglomerates highlights the potential for pseudo-colloid formation, explaining the basis of current particle filtration / abatement of technology. This study, which examines novel samples from a complex, highly radioactive facility using advanced techniques, provides a new understanding of radionuclide speciation and mobility in these environments and informs radioactive effluent treatment and disposal.