Published March 21, 2015 | Version v1
Journal article

Nuclear waste viewed in a new light; a synchrotron study of uranium encapsulated in grout

  • 1. Interface Analysis Centre, H. H. Wills Physics Laboratory, University of Bristol, Tyndall Avenue, Bristol BS8 1TL (United Kingdom)
  • 2. Diamond Light Source Limited, Harwell Science and Innovation Campus, Fermi Avenue, Didcot, Oxfordshire OX11 0QX (United Kingdom)
  • 3. National Nuclear Laboratory, Seascale, Cumbria CA20 1 PG (United Kingdom)
  • 4. Radioactive Waste Management Limited (formerly the Radioactive Waste Management Directorate of the UK Nuclear Decommissioning Authority), Curie Avenue, Didcot, Oxfordshire OX11 0RH (United Kingdom)

Description

Highlights: • Unirradiated Magnox uranium was encapsulated in grout and exposed to hydrogen. • Synchrotron X-ray tomography imaged the uranium corrosion before and after exposure. • Synchrotron X-ray powder diffraction identified the corrosion products; UH3 and UO2. • Uranium encapsulated in grout oxidised via the anoxic U + H2O regime. • Successful in-situ, non-invasive examination of pyrophoric and radioactive material - Abstract: How do you characterise the contents of a sealed nuclear waste package without breaking it open? This question is important when the contained corrosion products are potentially reactive with air and radioactive. Synchrotron X-rays have been used to perform micro-scale in-situ observation and characterisation of uranium encapsulated in grout; a simulation for a typical intermediate level waste storage packet. X-ray tomography and X-ray powder diffraction generated both qualitative and quantitative data from a grout-encapsulated uranium sample before, and after, deliberately constrained H2 corrosion. Tomographic reconstructions provided a means of assessing the extent, rates and character of the corrosion reactions by comparing the relative densities between the materials and the volume of reaction products. The oxidation of uranium in grout was found to follow the anoxic U + H2O oxidation regime, and the pore network within the grout was observed to influence the growth of uranium hydride sites across the metal surface. Powder diffraction analysis identified the corrosion products as UO2 and UH3, and permitted measurement of corrosion-induced strain. Together, X-ray tomography and diffraction provide means of accurately determining the types and extent of uranium corrosion occurring, thereby offering a future tool for isolating and studying the reactions occurring in real full-scale waste package systems

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jhazmat.2014.11.035

Additional details

Identifiers

DOI
10.1016/j.jhazmat.2014.11.035;
PII
S0304-3894(14)00942-X;

Publishing Information

Journal Title
Journal of Hazardous Materials
Journal Volume
285
Journal Page Range
p. 221-227
ISSN
0304-3894
CODEN
JHMAD9

Optional Information

Copyright
Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.