Leaching behaviour and α-decay damage accumulation of UO2 containing short-lived actinides
- 1. Institute for Transuranium Elements, Karlsruhe (Germany). European Commission
- 2. CIEMAT, Madrid (Spain)
Description
UO2 containing short-lived α-emitters, the so-called α-doped UO2, can simulate type (i.e. a-decay) and level of activity of spent fuel at the time when it might become exposed to groundwater in a geologic repository during storage. This allows studying α-radiolysis effects on the dissolution of the fuel matrix. Additionally, UO2 with high concentrations of α-emitters accumulate, during experimentally acceptable short times, the amount of decays, hence of property modifications, corresponding to long storage times for spent fuel. UO2 containing ∼10 and ∼0.1 wt% 238Pu was fabricated and tested. Leaching experiments in deionized water under unaerated conditions, with continuous monitoring of the evolution of the redox potential and pH in the leaching solutions, were performed. The Eh measurements showed a fast increase of the redox potential in the case of the material with the highest α-activity, while theUO2 containing ∼0.1 wt% 238Pu increased its potential more slowly. The redox potential for undoped UO2 decreased steadily during the experiment. As previously observed, higher fractions of U were released in the case of α-doped UO2 compared to undoped UO2. The fractions of U and Pu released during leaching from the α-doped materials were very similar, suggesting that congruent dissolution occurred. After leaching times longer than 10h, only dissolved species were present in the solutions. Under these experimental conditions, characterized by relatively low values of the ratio sample surface/leachant volume, a dependence of the released amounts on the α-activity of the samples was observed. Periodical measurements of parameters like hardness, showed a rapid buildup of radiation damage in the material with the high α-activity. After more than two years, noticeable changes, namely an increase of the hardness, have begun to be observed also for the material with the low concentration of 238Pu. Copyright (2001) Material Research Society
Additional details
Identifiers
- URL
- http://www.mrs.org/;
Publishing Information
- Publisher
- Materials Research Society
- Imprint Place
- Warrendale, PA (United States)
- ISBN
- 1-55899-598-6
- Imprint Title
- Scientific basis for nuclear waste management XXIV: Materials Research Society symposium proceedings: Volume 663
- Imprint Pagination
- 1232 p.
- Journal Page Range
- p. 391-398
- ISSN
- 0275-0112
Conference
- Title
- Scientific basis for nuclear waste management XXIV
- Dates
- 27-31 Aug 2000
- Place
- Sydney, NSW (Australia)
INIS
- Country of Publication
- United States
- Country of Input or Organization
- Australia
- INIS RN
- 34038765
- Subject category
- S12: MANAGEMENT OF RADIOACTIVE WASTES, AND NON-RADIOACTIVE WASTES FROM NUCLEAR FACILITIES;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- ALPHA-BEARING WASTES; GROUND WATER; LEACHING; PH VALUE; PHYSICAL RADIATION EFFECTS; PLUTONIUM 238; RADIATION HARDENING; RADIOLYSIS; REDOX POTENTIAL; SPENT FUELS; URANIUM OXIDES
- Descriptors DEC
- ACTINIDE COMPOUNDS; ACTINIDE NUCLEI; ALPHA DECAY RADIOISOTOPES; CHALCOGENIDES; CHEMICAL RADIATION EFFECTS; CHEMICAL REACTIONS; DECOMPOSITION; DISSOLUTION; ENERGY SOURCES; EVEN-EVEN NUCLEI; FUELS; HARDENING; HEAVY ION DECAY RADIOISOTOPES; HEAVY NUCLEI; HYDROGEN COMPOUNDS; ISOTOPES; MATERIALS; NUCLEAR FUELS; NUCLEI; OXIDES; OXYGEN COMPOUNDS; PHYSICAL RADIATION EFFECTS; PLUTONIUM ISOTOPES; RADIATION EFFECTS; RADIOACTIVE MATERIALS; RADIOACTIVE WASTES; RADIOISOTOPES; REACTOR MATERIALS; SEPARATION PROCESSES; SILICON 32 DECAY RADIOISOTOPES; SPONTANEOUS FISSION RADIOISOTOPES; URANIUM COMPOUNDS; WASTES; WATER; YEARS LIVING RADIOISOTOPES
Optional Information
- Notes
- 23 refs., 1 tabs., 4 figs.