The effects of alpha-radiolysis on UO2 dissolution determined from electrochemical experiments with 238Pu-doped UO2

2002 ◽  
Vol 90 (9-11) ◽  
Author(s):  
S. Stroes-Gascoyne ◽  
F. King ◽  
J. S. Betteridge ◽  
F. Garisto

SummaryThe long-term stability of spent nuclear fuel under deep geologic repository conditions will be determined mostly by the influence of α-radiolysis, since the dose-rate for α-radiolysis will exceed that for γ/β-radiolysis beyond a fuel age of ∼100 years and will persist for more than 10000 years. Dissolution rates derived from studies with currently available spent fuel include radiolysis effects from γ/β- as well as α-radiolysis. The use of external α-sources and chemically added H

Author(s):  
Juan Merino ◽  
Xavier Gaona ◽  
Lara Duro ◽  
Jordi Bruno ◽  
Aurora Marti´nez-Esparza

The study of spent fuel behaviour under disposal conditions is usually based on conservative approaches assuming oxidising conditions produced by water radiolysis at the fuel/water interface. However, the presence of H2 from container corrosion can inhibit the dissolution of the UO2 matrix and enhance its long-term stability. Several studies have confirmed the decrease in dissolution rates when H2 is present in the system, although the exact mechanisms of interaction have not been fully established. This paper deals with a radiolytic modelling exercise to explore the consequences of the interaction of H2 with radicals generated by radiolysis in the homogeneous phase. The main conclusion is that in all the modelled cases the presence of H2 in the system leads to a decrease in matrix dissolution. The extent of the inhibition, and the threshold partial pressure for the inhibition to take place, both depend in a complex way on the chemical composition of the water and the type of radiation present in the system.


1998 ◽  
Vol 121 (2) ◽  
pp. 174-188 ◽  
Author(s):  
Bernd Grambow ◽  
Andreas Loida ◽  
Emmanuel Smailos

1997 ◽  
Vol 506 ◽  
Author(s):  
E. C. Buck ◽  
R. J. Finch ◽  
P. A. Finn ◽  
J. K. Bates

ABSTRACTUranyl oxide hydrate phases are known to form during contact of oxide spent nuclear fuel with water under oxidizing conditions; however, less is known about the fate of fission and neutron capture products during this alteration. We describe, for the first time, evidence that neptunium can become incorporated into the uranyl secondary phase, dehydrated schoepite (UO3•0.8H2O). Based on the long-term durability of natural schoepite, the retention of neptunium in this alteration phase may be significant during spent fuel corrosion in an unsaturated geologic repository.


Author(s):  
Krista Nicholson ◽  
John McDonald ◽  
Shona Draper ◽  
Brian M. Ikeda ◽  
Igor Pioro

Currently in Canada, spent fuel produced from Nuclear Power Plants (NPPs) is in the interim storage all across the country. It is Canada’s long-term strategy to have a national geologic repository for the disposal of spent nuclear fuel for CANada Deuterium Uranium (CANDU) reactors. The initial problem is to identify a means to centralize Canada’s spent nuclear fuel. The objective of this paper is to present a solution for the transportation issues that surround centralizing the waste. This paper reviews three major components of managing and the transporting of high-level nuclear waste: 1) site selection, 2) containment and 3) the proposed transportation method. The site has been selected based upon several factors including proximity to railways and highways. These factors play an important role in the site-selection process since the location must be accessible and ideally to be far from communities. For the containment of the spent fuel during transportation, a copper-shell container with a steel structural infrastructure was selected based on good thermal, structural, and corrosion resistance properties has been designed. Rail has been selected as the method of transporting the container due to both the potential to accommodate several containers at once and the extensive railway system in Canada.


1994 ◽  
Vol 353 ◽  
Author(s):  
Jordi Bruno ◽  
I. Casas ◽  
E. Cera ◽  
J. de Pablo ◽  
J. GimÉnez ◽  
...  

AbstractWe have carried out an experimental comparison study of the dissolution rates of unirradiated UO2 and SIMFUEL pellets and particles (100–300 μm) in a standard NaCI/NaHC03 solution, under oxidizing conditions. We have performed the experiments using batch and flow methodologies. Both methodologies gave similar results, indicating that the overall oxidation/dissolution process is the same in both cases. The results from the experiments indicate that under these conditions the dissolution process is both oxygen and bicarbonate promoted. The dissolution rates we obtained are: R=2.4 ± 0.8 mg U/m2 d for U02 and R= 0.17 ± 0.05 mg U/m2 d for SIMFUEL. The results of the experiments indicate that the dissolution rate under oxic conditions is clearly dependent on the number of U(VI) surface sites which for spent nuclear fuel is a function of the extent of radiolytic oxidation.


1981 ◽  
Vol 11 ◽  
Author(s):  
B. Allard ◽  
U. Olofsson ◽  
B. Torstenfelt ◽  
H. Kipatsi ◽  
K. Andersson

The long-lived actinides and their daughter products largely dominate the biological hazards from spent nuclear fuel already from some 300 years after the discharge from the reactor and onwards . Therefore it is essential to make reliable assessments of the geochemistry of these elements in any concept for long-term storage of spent fuel or reprocessing waste, etc.


2004 ◽  
Vol 824 ◽  
Author(s):  
Christophe Poinssot ◽  
Patrick Lovera ◽  
Cécile Ferry

AbstractIn the framework of the research conducted on the long term evolution of spent nuclear fuel in geological disposal conditions, a source term model has been developed to evaluate the instantaneous release of RN (Instant Release Fraction IRF) and the delayed release of the RN which are embedded within the matrix. This model takes into account all the scientific results currently available in the literature except the hydrogen effect. IRF was assessed by considering the evolution with time of the RN inventories located within the fuel microstructure to which no confinement properties can be allocated on the long term (rim, gap, grain boundaries). It allows to propose some reference bounding values for the IRF as a function of time of canister breaching and burnup. The matrix radiolytic dissolution was modeled by a simple kinetic model neglecting the radiolytic species recombination and the influence of aqueous ligands and radiolytic oxidants were supposed to completely react with the fuel surface. Spent fuel performance was therefore demonstrated to deeply depend on the reactive surface area.


2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
B. Yolanda Moratilla Soria ◽  
Maria Uris Mas ◽  
Mathilde Estadieu ◽  
Ainhoa Villar Lejarreta ◽  
David Echevarria-López

The objective of the present study is to compare the associated costs of long-term storage of spent nuclear fuel—open cycle strategy—with the associated cost of reprocessing and recycling strategy of spent fuel—closed cycle strategy—based on the current international studies. The analysis presents cost trends for both strategies. Also, to point out the fact that the total cost of spent nuclear fuel management (open cycle) is impossible to establish at present, while the related costs of the closed cycle are stable and known, averting uncertainties.


Author(s):  
Edgar C. Buck ◽  
Nancy L. Dietz ◽  
John K. Bates

Direct disposal of spent nuclear fuel (SNF) into the proposed unsaturated geologic repository at Yucca Mountain, NV is being studied at several laboratories, including Argonne National Laboratory. Corrosion tests with SNF are being conducted to understand the long-term behavior of SNF under conditions designed to simulate the unsaturated conditions at the site. The SNF used in this study was the Approved Testing Material (ATM)-106 with a bum-up of 43 MW·d/kg U. A sample of ATM-106 fuel was exposed to dripping simulated groundwater for 271 days; after this time the experiment was terminated and the material removed for further study. Details of the testing methodology have been given by Finn et al.,.Previous attempts to study SNF with TEM have used ion milled samples, in this study we prepared the samples by ultramicrotomy which reduced the radiological hazard substantially.


Author(s):  
Sergey Yu. Sayenko ◽  
G. A. Kholomeyev ◽  
B. A. Shilyaev ◽  
A. V. Pilipenko ◽  
E. P. Shevyakova ◽  
...  

Abstract This paper describes the research work carried out at the NSC KIPT to develop and apply a final waste form in the shape of a monolithic solid block for the containment of spent nuclear fuel. To prepare radioactive waste for long-term storage and final deep geological disposal, investigations into the development of methods of immobilizing HLW simulators in protective solid matrices are being conducted at the NSC KIPT. For RBMK spent nuclear fuel it is proposed and justified to encapsulate the spent fuel bundles into monolithic protective blocks, produced with the help of hot isostatic pressing (HIP) of powder materials. In accordance with this approach, as a material for the protective block made up of the glass-ceramic composition prepared by sintering at isostatic pressure, the powder mixture of such natural rocks as granite and clay has been chosen. Concept approach and characterization of waste form, technological operations of manufacturing and performance assessment are presented. The container with spent fuel for long-term storage and final disposal presents a three barrier protective system: ceramic fuel UO2 in cladding tube, material of the glass-ceramic block, material of the sealed metal capsule. Investigations showed that the produced glass-ceramic material is characterized by high stability of chemical and phase compositions, high resistance in water medium, low porosity (compared with the porosity of natural basalt). With the help of mathematical calculations it was shown that the absorbed dose of immobilizing material by RBMK spent fuel irradiation for 1000 years of storage in the geological disposal after 10 years of preliminary cooling will be ∼ 3.108 Gy, that is 2–3 orders of magnitude less than the values corresponding to preserving radiation resistance and functional parameters of glasses and ceramics. The average value of velocity of linear corrosion in water medium of the protective layer made up of the glass-ceramic composition determined experimentally makes up ∼ 15 mm per year. This allows to use glass-ceramic compositions effectively as an engineering barrier in the system of spent fuel geological disposal and to increase the lifetime of the waste container, in particular, up to 3000 years with the layer thickness ∼ 40 mm. The possible release of radionuclides from the waste container during its interim storage in the open air (near-surface storage) is estimated. The calculations are made by taking into account the possible increase of coefficients of radionuclide diffusion from 10−16 to 10−14 m2/c as a result of spent fuel radiation affecting the protective layer. The obtained results showed that the protective barrier (about 40 mm) at the base of the glass-ceramic composition, ensures reliable isolation from the environment against the release of radionuclides from the controlled near-surface long-term storage far up to 1000 years. The relatively limited release of radionuclides will make up about 1% for the period of more than 400 years, and 10% - in 1000 years. During this period of time, the radionuclides 90Sr and 137Cs will completely turn into stable 90Zr and 137Ba and the decay of many transuranium elements will occur. The results from laboratory scale experiments, tests and calculations carried out so far, show that the proposed glass-ceramic materials may be used as basic materials for manufacturing the monolithic protective block in which the spent fuel elements will be embedded with the aim of further long-term storage or final disposal.


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