Nuclear waste viewed in a new light; a synchrotron study of uranium encapsulated in grout
Creators
- 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.2014.11.035Additional 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
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47030806
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- COMPARATIVE EVALUATIONS; CORROSION; CORROSION PRODUCTS; GROUTING; HYDROGEN; INTERMEDIATE-LEVEL RADIOACTIVE WASTES; MAGNOX; OXIDATION; POWDERS; TOMOGRAPHY; URANIUM; URANIUM DIOXIDE; URANIUM HYDRIDES; X-RAY DIFFRACTION
- Descriptors DEC
- ACTINIDE COMPOUNDS; ACTINIDES; ALLOYS; CHALCOGENIDES; CHEMICAL REACTIONS; COHERENT SCATTERING; DIAGNOSTIC TECHNIQUES; DIFFRACTION; ELEMENTS; EVALUATION; HYDRIDES; HYDROGEN COMPOUNDS; MAGNESIUM ALLOYS; MAGNESIUM BASE ALLOYS; MATERIALS; METALS; NONMETALS; OXIDES; OXYGEN COMPOUNDS; RADIOACTIVE MATERIALS; RADIOACTIVE WASTES; SCATTERING; URANIUM COMPOUNDS; URANIUM OXIDES; WASTES
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.