Dry Pretreatment of Used Nuclear Fuel for Tritium Removal: A Review
- Oak Ridge National Laboratory, P.O. Box 2008, Oak Ridge, TN 37831-6243 (United States)
Virtually all the elements in the periodic chart are generated as a result of atomic fission in nuclear fuel. Several of the elements are volatile or can readily react with other chemicals to form volatile molecules that can be released during the processing of used nuclear fuel for the recovery of the valuable products. Among the volatile fission products, {sup 129}I, {sup 14}C, {sup 3}H, {sup 85}Kr, and {sup 79}Se constitute the main environmental concern for uncontrolled release. Storage of used fuel allows the short-lived isotopes to decay significantly (e.g., {sup 3}H decays in half every 12.32 years and {sup 85}Kr every 10.76 years). However, depending on regulatory limits they may remain an environmental concern up to about 50-100 years of fuel storage. In contrast, the concern for environmental release of the highly mobile {sup 129}I and {sup 14}C remains for geological times (half-lives of 15.7 million years for {sup 129}I and 5730 years for {sup 14}C). Processing of used commercial nuclear fuel requires significant head-end operations to remove the fuel from the protective coverings (e.g., assemblies). The current industrial process includes cropping the end caps of the fuel assemblies, chopping of the fuel pins and/or bundles into short segments, and prolonged leaching of the segments using concentrated nitric acid (HNO{sub 3}). The infrastructure, processes, and waste treatment systems in the head-end operations, including the associated off-gas system, are some of the larger and more costly components of the entire plant. The bulk of the volatile fission products are released to the off-gas during the leaching and dissolution. However, a small but significant amount will transfer to the following steps of processing such as solvent extraction and will show up in many different waste streams. The effective capture of {sup 3}H and iodine throughout the different processes and disposition of associated waste streams is costly and complicated. Up-front removal and capture is highly desirable. Currently, at the U.S. Department of Energy national laboratories and internationally, several dry pretreatment technologies are being studied and developed with the potential to simplify and increase the safety of subsequent storage or chemical recycling processes. These studies include (1) alternative decladding methods, (2) oxidation of exposed fuel following either conventional shearing or chemical decladding, and (3) the collection and stabilization of released volatile radionuclides. Several dry processes are being developed for the up-front removal of tritium and other fission products. They can be combined with different decladding alternatives and, in general, produce a fine powder that can be fed to aqueous or pyrochemical separations processes. (authors)
- OSTI ID:
- 22991830
- Journal Information:
- Transactions of the American Nuclear Society, Vol. 114, Issue 1; Conference: Annual Meeting of the American Nuclear Society, New Orleans, LA (United States), 12-16 Jun 2016; Other Information: Country of input: France; 6 refs.; Available from American Nuclear Society - ANS, 555 North Kensington Avenue, La Grange Park, IL 60526 United States; ISSN 0003-018X
- Country of Publication:
- United States
- Language:
- English
Similar Records
Graphite fuels combustion off-gas treatment options
Multicomponent adsorption of radioactive iodine and krypton using ETS-10 supported carbon nano-polyhedrons