A Study of Flammable Gas Generation and Radionuclide Release during Underwater Handling of AM Reactor Spent Fuel

2021 ◽  
Vol 2021 (2) ◽  
pp. 71-80
Author(s):  
Artem Zuferovich Gaiazov ◽  
Leshchenko A.Yu. Leshchenko ◽  
Valery Pavlovich Smirnov ◽  
Pavel Aleksandrovich Ilyin ◽  
Vladimir Gennadievich Teplov
2021 ◽  
Vol 7 (3) ◽  
pp. 223-229
Author(s):  
Artyom Z. Gayazov ◽  
Anton Yu. Leshchenko ◽  
Valery P. Smirnov ◽  
Pavel A. Ilyin ◽  
Vadim G. Teplov

Introduction. The paper addresses studies on the accumulation of combustible gases during underwater handling simulations for the leaky spent nuclear fuel from the AM reactor. Two fuel compositions were studied- uranium-molybdenum dispersed in magnesium and uranium carbide dispersed in calcium. Methods. The 137Cs release rate was measured during underwater storage of the uranium-molybdenum fuel. The kinetics of hydrogen release for both fuels and methane release for the carbide SNF were obtained. The kinetics approximate most with exponential dependences that formally correspond to first-order chemical reactions. A contribution of radiolytic hydrogen to the gases generated during the experiments was estimated. It was demonstrated that the determining source of the gases is the chemical interaction between the spent fuel and the water. The experiment with the uranium-molybdenum fuel demonstrated a pronounced passivation effect of the chemical processes on the fuel surface due to insoluble corrosion products. For the carbide SNF, an incubation period of about 20 hours was observed followed by an intensive release of hydrogen and methane. Results. The obtained results were subject to a comparative analysis against publications on the behavior of the fuel components in water. Conclusion. The findings can be applied to justify fire and explosion safety of underwater handling techniques for the damaged spent nuclear fuel with the considered fuel compositions (the spent fuel from reactors AM, AMB, EGP-6, etc.), e.g., to justify underwater preparations of the AMB spent fuel for reprocessing.


1987 ◽  
Vol 112 ◽  
Author(s):  
Shirley A. Rawson ◽  
William L. Neal ◽  
James R. Burnell

AbstractThe Basalt Waste Isolation Project has conducted a series of hydrothermal experiments to characterize waste/barrier/rock interactions as a part of its study of the Columbia River basalts as a potential medium for a nuclear waste repository. Hydrothermal tests of 3–15 months duration were performed with light water reactor spent fuel and simulated groundwater, in combination with candidate container materials (low-carbon steel or copper) and/or basalt, in order to evaluate the effect of waste package materials on spent fuel radionuclide release behavior. Solutions were filtered through 400 and 1.8 nm filters to distinguish colloidal from dissolved species. In all experiments, 14C, 129I, and 137Cs occurred only as dissolved species, whereas the actinides occurred in 400 nm filtrates primarily as spent fuel particles. Actinide concentrations in 1.8 nm filtrates were below detection in steel-bearing experiments. In the system spent fuel + copper, apparent time-invariant concentrations of 14C and 137Cs were obtained, but in the spent fuel + steel system, the concentrations of 14C and 137Cs increased gradually throughout the experiments. In experiments containing basalt or steel + basalt, 137Cs concentrations decreased with time. In tests with copper + basalt, 14C and 129I concentrations attained time-invariant values and 137Cs concentrations decreased. Concentrations for the actinides and fission products measured in these experiments were below those calculated from Federal regulations governing radionuclide release.


2005 ◽  
Author(s):  
A. D. Cozzi ◽  
D. A. Crowley ◽  
J. M. Duffey ◽  
R. E. Eibling ◽  
T. M. Jones ◽  
...  

1987 ◽  
Vol 112 ◽  
Author(s):  
L. H. Johnson ◽  
D. W. Shoesmith ◽  
S. Stroes-Gascoyne

AbstractThe concept of disposal of unreprocessed spent fuel has now been under study internationally for over ten years. Considerable progress has been made in understanding the factors that will control radionuclide release from spent fuel in an underground disposal vault. This progress is reviewed and the research areas of significance in providing further data for source term models are discussed. Key areas for future research are identified; these include improved characterization of spent fuel to determine the inventories of fission products at grain boundaries, together with their release kinetics; and a better understanding of the effects of solution chemistry on spent fuel dissolution, in particular the effects of salinity, redox chemistry, and radiolysis of groundwater. Approaches to modelling the dissolution of spent fuel are discussed, and a possible approach for developing an oxidative dissolution model is outlined.


1989 ◽  
Vol 176 ◽  
Author(s):  
Bernd Grambow ◽  
L.O. Werme ◽  
R.S. Forsyth ◽  
J. Bruno

ABSTRACTComparison of spent fuel corrosion data from nuclear waste management projects in Canada, Sweden and the USA strongly suggests that the release of 90Sr to the leachant can be used as a measure of the degradation (oxidation/dissolution) of the fuel matrix. A surprisingly quantitative similarity in the 90 Sr release data for fuel of various types (BWR, PWR, Candu), linear power ratings and burnups leached under oxic conditions was observed in the comparison. After 1000 days of leachant contact, static or sequential, the fractional release rates for 90Sr (and for cesium nuclides) were of the order of 10−7/d.The rate of spent fuel degradation (alteration) under oxic conditions can be considered to be controlled either by the growth rates of secondary alteration products, by oxygen diffusion through a product layer, by the rate of formation of radiolytic oxidants or by solubility-controlled dissolution of the matrix. These processes are discussed. Methods for determining upper limits for long-term 90Sr release, and hence fuel degradation, have been derived from the experimental data and consideration of radiolytic oxidant production.


2012 ◽  
Vol 1475 ◽  
Author(s):  
I. G. McKinley ◽  
F. B. Neall ◽  
E. M. Scourse ◽  
H. Kawamura

ABSTRACTConcepts for the disposal of high-level radioactive waste (HLW) and spent fuel (SF) in several countries include a massive steel overpack within a bentonite buffer. In past conservative safety assessments to demonstrate feasibility of geological disposal, overpacks are assumed to provide complete containment for a given lifetime, after which all fail simultaneously. After failure, they are ignored as physical barriers to radionuclide transport. In order to compare different repository designs for specific sites, however, a more realistic treatment of overpack failure and its subsequent behaviour is needed. In addition to arguing for much longer lifetimes before mechanical failure and a distribution of overpack failure times, such assessment indicates that the presence of the failed overpack greatly constrains radionuclide release from the waste matrix and subsequent migration through the engineered barrier system. It also emphasises the key role of the bentonite buffer and the need to be able to assure its performance over relevant timescales.


1983 ◽  
Vol 26 ◽  
Author(s):  
D.E. Grandstaff ◽  
G.L. Mckeon ◽  
E.L. Moore ◽  
G.C. Ulmer

ABSTRACTThe Grande Ronde Basalts underlying the Hanford Site are being evaluated as a possible site for a high-level nuclear waste repository. Experiments, in which basalt from the Umtanun flow of the Grande Ronde Basalt and basalt with simulated spent fuel were reacted with synthetic Hanford groundwater, were conducted to determine steady state concentrations which can be used in radionuclide release-rate models. Tests were performed at temperatures of 100°, 200°, and 300°C; 30 MPa pressure, and a solution:solid mass ratio of 10:1 for durations up to 7,000 hr. Solution aliquots were extracted periodically during the experiments for analysis. The pH was measured at 250°C and recalculated to higher temperatures. In the basalt-water system the stable high-temperature pH values achieved were 7.2 (100°C), 7.5 (200°C), and 7.6 (300°C). Solution composition variations are due to mesostasis (glass) dissolution and precipitation of secondary phases. Solution measurements indicate a redox potential (Eh) of about -0.7 volts at 300°C. Secondary phases produced include silica, potassium feldspar, iron oxides, clays, scapolite, and zeolites. Tests in the basalt + simulated spent fuel + water systen show that calculated pH values stabilized near 7.6 (100°C), 7.2 (200°C), and 7.7 (300°C). At higher temperatures, solution concentrations were controlled by secondary phases similar to those found in basalt-water tests. Less than 1% of uranium, thorium, samarium, rhenium, cerium, and palladium were released to solution while somewhat higher amounts of iodine, molybdenum, and cesium were released. The UO2 component was unreactive; however, other components (e.g., cesium-bearing phases) were almost completely dissolved. Secondary phases incorporating radionuclide-analog elements include clays, palladium sulfide, powellite, coffinite, and a potassium-uranium silicate.


MRS Advances ◽  
2016 ◽  
Vol 1 (62) ◽  
pp. 4147-4156 ◽  
Author(s):  
C. Ferry ◽  
J. Radwan ◽  
H. Palancher

ABSTRACTHelium is produced in spent nuclear fuel by α-decays of actinides. After 10,000 years, the concentration of He accumulated in UO2 spent fuel is about 0.23 at.%. For direct disposal of spent nuclear fuel, consequences of helium build-up on the fuel matrix microstructure must be evaluated since it can modify the radionuclide release when water comes into contact with the spent fuel surface, after breaching of the disposal canister. An operational model has been proposed in order to evaluate the effect of helium on the microstructure of spent fuel in a repository. Based on conservative assumptions and different scenarios of bubble population, the calculated helium critical concentration, that could lead to a partial loss of integrity of the spent fuel pellet, is 0.37 at.%. However, observations on He-implanted UO2, α-doped UO2 pellets and natural analogues evidence a macroscopic damage only for He concentrations, which are more than one order of magnitude higher.


2005 ◽  
Vol 346 (1) ◽  
pp. 24-31 ◽  
Author(s):  
Andreas Loida ◽  
Volker Metz ◽  
Bernhard Kienzler ◽  
Horst Geckeis

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