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Title: Tritium Content in and Release from Pressurized-Water-Reactor Fuel Cladding

Journal Article · · Transactions of the American Nuclear Society
OSTI ID:22991826
; ; ;  [1]
  1. Oak Ridge National Laboratory, P.O. Box 2008, Oak Ridge, TN 37831-6152 (United States)

It is expected that tritium pretreatment will be required in future reprocessing plants to prevent the release of tritium to the environment (except for long-cooled fuels; >30 yrs). To design and operate future reprocessing plants in a safe and environmentally compliant manner, the amount and form of tritium in the used nuclear fuel (UNF) must be understood and quantified. Tritium in light water reactor (LWR) fuel is dispersed between the fuel matrix and the fuel cladding, and some tritium may be in the plenum, probably as tritiated water (THO or T{sub 2}O). In a standard processing flowsheet, tritium management would be accomplished by treatment of liquid streams within the plant. Pretreating the fuel prior to dissolution to release the tritium into a single off-gas stream could simplify tritium management, so the removal of tritium in the liquid streams throughout the plant may not be required. The fraction of tritium remaining in the cladding may be reduced as a result of tritium pretreatment. Since Zircaloy'R cladding makes up roughly 25% by mass of UNF in the United States, processes are being considered to reduce the volume of reprocessing waste attributed to Zircaloy'R clad fuel by recovering the zirconium from the cladding for reuse. Treatment options for Zircaloy cladding include recycling to recover the significant value of the zirconium and eliminate costs associated with the disposal of transuranic-contaminated Zircaloy. If LWR fuel is reprocessed and the fuel is dissolved without tritium pretreatment, the tritium in the cladding will remain bound to the cladding. If tritium pretreatment is included in the flow sheet, some portion of the tritium in the cladding may be released along with the tritium from the fuel matrix. To design and operate reprocessing plants in a safe and environmentally compliant manner, the amount and form of tritium in the UNF must be understood and quantified. For Zircaloy-clad fuels from light water reactors, the tritium produced from ternary fission and other sources is expected to be divided between the fuel, where it is generated, and the cladding. It has been previously documented that a fraction of the tritium produced in uranium oxide fuel from LWRs can migrate and become trapped in the cladding. Estimates of the percentage of tritium in the cladding typically range from 0-96%. There is relatively limited data on how the tritium content of the cladding varies with burnup and fuel history (temperature, power, etc.) and how pretreatment impacts its release. The present study was undertaken to understand how tritium pretreatment at standard tritium pretreatment conditions (oxidation in air at 480 to 600 deg. C) affects the tritium content in the Zircaloy cladding and the extent to which the tritium content could be reduced with modest increases in the tritium pretreatment temperature. The data indicate that <20% of the tritium in PWR cladding will be removed by pretreatment at 500-700 deg. C for 24 h. Essentially 100% of the tritium will likely be released if the heating time at 700 deg. C is extended to 96 h. Small amounts of tritium are expected to be released if the cladding is heated at ≤ 600 deg. C for up to 96 h. The results of this study indicate that the amount of tritium released from tritium pretreatment systems will be dependent on both the operating temperature and length of time in the pretreatment system. Under certain conditions, a significant fraction of the tritium could remain bound in the cladding and would need to be considered in any subsequent processing of the cladding to recover/recycle the zirconium. (authors)

OSTI ID:
22991826
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; 1 ref.; 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