The Assessment of the Long-Term Evolution of the Spent Nuclear Fuel Matrix by Kinetic, Thermodynamic and Spectroscopic Studies of Uranium Minerals.

1994 ◽  
Vol 353 ◽  
Author(s):  
Jordi Bruno ◽  
I. Casas ◽  
E Cera ◽  
R. C. Ewing ◽  
R. J. Finch ◽  
...  
Keyword(s):  
Nuclear Fuel ◽  
Safety Assessment ◽  
Source Term ◽  
Spent Nuclear Fuel ◽  
Spectroscopic Studies ◽  
Spent Fuel ◽  
Term Evolution ◽  
Uranium Minerals ◽  
The Stability

AbstractThe long term behaviour of spent nuclear fuel is discussed in the light of recent thermodynamic and kinetic data on mineralogical analogues related to the key phases in the oxidative alteration of uraninite. The implications for the safety assessment of a repository of the established oxidative alteration sequence of the spent fuel matrix are illustrated with Pagoda calculations. The application to the kinetic and thermodynamic data to source term calculations indicates that the appearance and duration of the U(VI) oxyhydroxide transient is critical for the stability of the fuel matrix.

scholarly journals An Automated SeaFAST ICP-DRC-MS Method for the Determination of 90Sr in Spent Nuclear Fuel Leachates

Molecules ◽  
2020 ◽  
Vol 25 (6) ◽  
pp. 1429 ◽  
Author(s):  
Víctor Vicente Vilas ◽  
Sylvain Millet ◽  
Miguel Sandow ◽  
Luis Iglesias Pérez ◽  
Daniel Serrano-Purroy ◽  
...  
Keyword(s):  
Nuclear Fuel ◽  
Safety Assessment ◽  
Analytical Approach ◽  
Source Term ◽  
Spent Nuclear Fuel ◽  
Spent Fuel ◽  
Chemical Purification ◽  
Radiochemical Method ◽  
Good Agreement

To reduce uncertainties in determining the source term and evolving condition of spent nuclear fuel is fundamental to the safety assessment. ß-emitting nuclides pose a challenging task for reliable, quantitative determination because both radiometric and mass spectrometric methodologies require prior chemical purification for the removal of interfering activity and isobars, respectively. A method for the determination of 90Sr at trace levels in nuclear spent fuel leachate samples without sophisticated and time-consuming procedures has been established. The analytical approach uses a commercially available automated pre-concentration device (SeaFAST) coupled to an ICP-DRC-MS. The method shows good performances with regard to reproducibility, precision, and LOD reducing the total time of analysis for each sample to 12.5 min. The comparison between the developed method and the classical radiochemical method shows a good agreement when taking into account the associated uncertainties.

New Perspectives for the Spent Nuclear Fuel Radionuclides Release Model in a Deep Geological Repository

2006 ◽  
Vol 985 ◽  
Author(s):  
Christophe Poinssot ◽  
Cécile FERRY ◽  
Arnaud POULESQUEN
Keyword(s):  
Nuclear Fuel ◽  
Source Term ◽  
Spent Nuclear Fuel ◽  
Deep Geological Repository ◽  
Term Evolution ◽  
Geological Repository ◽  
Definition Of ◽  
Release Model ◽  
The Impact

AbstractSpent Nuclear Fuel (SNF) source terms are used to define the release rate of radionuclides (RN) in a direct disposal and to assess the performance of this waste form. They classically distinguish between two contributions: (i) the Instant Release Fraction (IRF) of RN which are directly leached when water contacts the fuel, (ii) the slow and long term release of RN which are embedded within the fuel matrix. Recent experimental results bring significant input in our understanding and assessment of both contributions. However, they have not yet been integrated in the definition of the SNF source term. This paper will present the impact on the RN source term of the latest results on the SNF long term evolution and the key remaining scientific issues.

Consequences of the Anticipated Long-Term Evolution of Spent Nuclear Fuel for the Assessment of the Release Rate of Radionuclides.

2002 ◽  
Vol 757 ◽  
Author(s):  
Christophe Poinssot ◽  
Patrick Lovera ◽  
Cécile Ferry ◽  
Jean-Marie Gras
Keyword(s):  
Nuclear Fuel ◽  
Source Term ◽  
Spent Nuclear Fuel ◽  
Long Term Evolution ◽  
Time Dependent ◽  
Geological Disposal ◽  
Long Term Storage ◽  
Term Evolution ◽  
Term Storage

ABSTRACTThe research conducted in the framework of the French research project on spent nuclear fuel (SNF) long - term evolution (PRECCI Project) has enlightened the potential significance of spent nuclear fuel intrinsic evolution in closed system for the assessment of radionuclide (RN) source term in long-term storage or geological disposal. Beyond others, alpha self-irradiation enhanced diffusion and evolution of the grain boundaries cohesion are two major processes which have to be accounted for in view of the RN source term models development. Accounting for these processes, operational models are developed, the aim of which is to quantitatively define the RN release rates from SNF in long-term storage or geological disposal. They distinguish basically an instantaneous contribution (IRF in geological disposal) and a time-dependent contribution (matrix oxidation or alteration). RN inventories associated to these two different processes have to be modeled since they are time-dependent due to the RN diffusion within the pellet. The present paper details the models that are developed in France in terms of assumptions, conservatism and robustness. It comes out from this work that for the instant release fraction, we have to consider a much higher instant release fraction than classically assumed (5–6% in geological disposal) in particular for geological disposal.

scholarly journals An Alternative Conceptual Model for the Spent Nuclear Fuel–Water Interaction in Deep Geologic Disposal Conditions

2021 ◽  
Vol 11 (18) ◽  
pp. 8566
Author(s):  
Barbara Pastina ◽  
Jay A. LaVerne
Keyword(s):  
Conceptual Model ◽  
Nuclear Fuel ◽  
Release Rate ◽  
Safety Assessment ◽  
Spent Nuclear Fuel ◽  
Water Radiolysis ◽  
Spent Fuel ◽  
Radiation Chemical ◽  
Radionuclide Release

For the long-term safety assessment of direct disposal of spent nuclear fuel in deep geologic repositories, knowledge on the radionuclide release rate from the UO2 matrix is essential. This work provides a conceptual model to explain the results of leaching experiments involving used nuclear fuel or simulant materials in confirmed reducing conditions. Key elements of this model are: direct effect of radiation from radiolytic species (including defects and excited states) in the solid and in the first water layers in contact with its surface; and excess H2 may be produced due to processes occurring at the surface of the spent fuel and in confined water volumes, which may also play a role in keeping the spent fuel surface in a reduced state. The implication is that the fractional radionuclide release rate used in most long-term safety assessments (10−7 year−1) is over estimated because it assumes that there is net UO2 oxidation caused by radiolysis, in contrast with the alternative conceptual model presented here. Furthermore, conventional water radiolysis models and radiation chemical yields published in the literature are not directly applicable to a heterogeneous system such as the spent fuel–water interface. Suggestions are provided for future work to develop more reliable models for the long-term safety assessment of spent nuclear fuel disposal.

Landscape Modeling for Dose Calculations in the Safety Assessment of a Repository for Spent Nuclear Fuel

2007 ◽  
Author(s):  
Tobias Lindborg ◽  
Ulrik Kautsky ◽  
Lars Brydsten
Keyword(s):  
Nuclear Fuel ◽  
Safety Assessment ◽  
Spent Nuclear Fuel ◽  
Landscape Model ◽  
Landscape Development ◽  
Surface Hydrology ◽  
Site Investigations ◽  
Time Period ◽  
The Individual

The Swedish Nuclear Fuel and Waste Management Co., (SKB), pursues site investigations for the final repository for spent nuclear fuel at two sites in the south eastern part of Sweden, the Forsmark- and the Laxemar site (figure 1). Data from the two site investigations are used to build site descriptive models of the areas. These models describe the bedrock and surface system properties important for designing the repository, the environmental impact assessment, and the long-term safety, i.e. up to 100,000 years, in a safety assessment. In this paper we discuss the methodology, and the interim results for, the landscape model, used in the safety assessment to populate the Forsmark site in the numerical dose models. The landscape model is built upon ecosystem types, e.g. a lake or a mire, (Biosphere Objects) that are connected in the landscape via surface hydrology. Each of the objects have a unique set of properties derived from the site description. The objects are identified by flow transport modeling, giving discharge points at the surface for all possible flow paths from the hypothetical repository in the bedrock. The landscape development is followed through time by using long-term processes e.g. shoreline displacement and sedimentation. The final landscape model consists of a number of maps for each chosen time period and a table of properties that describe the individual objects which constitutes the landscape. The results show a landscape that change over time during 20,000 years. The time period used in the model equals the present interglacial and can be used as an analogue for a future interglacial. Historically, the model area was covered by sea, and then gradually changes into a coastal area and, in the future, into a terrestrial inland landscape. Different ecosystem types are present during the landscape development, e.g. sea, lakes, agricultural areas, forest and wetlands (mire). The biosphere objects may switch from one ecosystem type to another during the modeled time period, from sea to lake, and from lake to mire and finally, some objects are transformed into agricultural area due to favorable farming characteristics.

Radionuclide Inventory of Vitrified Waste After Spent Nuclear Fuel Reprocessing at La Hague

2013 ◽  
Author(s):  
A. Meleshyn ◽  
U. Noseck
Keyword(s):  
Nuclear Fuel ◽  
Safety Assessment ◽  
Spent Nuclear Fuel ◽  
Auxiliary Information ◽  
Opalinus Clay ◽  
High Level Waste ◽  
Stable Elements ◽  
High Level ◽  
Model Approach

The primary aim of the present work was to determine the inventories of the radionuclides and stable elements in vitrified high-level waste produced at La Hague and delivered to Germany, which are of importance for long-term safety assessment of final repositories for radioactive wastes. For a subset of these radionuclides and stable elements, the inventories were determined — either by direct measurements or by involving established correlations — and reported by AREVA. This allowed verification of the validity of application of a model approach utilizing the data of burnup and activation calculations and auxiliary information on the reprocessing and vitrification process operated at La Hague. Having proved that such a model approach can be applied for prediction of inventories of actinides, fission and activation products in vitrified waste, the present work estimated the minimum, average and maximum inventories of the radionuclides, which are of importance for long-term safety assessment of final repositories for radioactive waste but were not reported by AREVA for delivered CSD-V canisters. The average and maximum inventories in individual CSD-V canisters predicted in the present approach were compared to the inventories predicted by Nagra for canisters with vitrified waste delivered from La Hague to Switzerland [1]. This comparison revealed a number of differences between these inventories despite the fact that the canisters delivered to Switzerland were produced in essentially the same way and from the common reprocessing waste stock as CSD-V canisters delivered to Germany. Therefore, a further work is required in order to identify the reason for the discrepancy in the present estimation versus the Nagra estimation [1]. Such a work should also address the recommendation by the international peer review of the Safety Report of the Project Opalinus Clay to obtain estimates of the inventories of long-lived mobile radionuclides (such as 14C, 36Cl, 79Se, and 129I), which contribute most to the dose estimates in the radiological safety assessments, if possible, in agreement with other countries with similar waste streams in order for a coordinated set of data to be generated [2]. Since vitrified waste from reprocessing of spent nuclear fuel at La Hague was delivered to several countries — Belgium, France, Germany, Japan, Netherlands, and Switzerland — an international effort can be recommended.

scholarly journals Approaches to Safety Justification for Loading of VSC-VVER Containers in ZNPP DSFSF

2019 ◽  
pp. 82-87
Author(s):  
Ya. Kostiushko ◽  
O. Dudka ◽  
Yu. Kovbasenko ◽  
A. Shepitchak
Keyword(s):  
Nuclear Fuel ◽  
Nuclear Power ◽  
Safety Assessment ◽  
Power Plants ◽  
Spent Nuclear Fuel ◽  
Operating Conditions ◽  
Spent Fuel ◽  
Fuel Assemblies ◽  
Fuel Storage ◽  
The Government

The introduction of new fuel for nuclear power plants in Ukraine is related to obtaining a relevant license from the regulatory authority for nuclear and radiation safety of Ukraine. The same approach is used for spent nuclear fuel (SNF) management system. The dry spent fuel storage facility (DSFSF) is the first nuclear facility created for intermediate dry storage of SNF in Ukraine. According to the design based on dry ventilated container storage technology by Sierra Nuclear Corporation and Duke Engineering and Services, ventilated storage containers (VSC-VVER) filled with SNF of VVER-1000 are used, which are located on a special open concrete site. Containers VSC-VVER are modernized VSC-24 containers customized for hexagonal VVER-1000 spent fuel assemblies. The storage safety assessment methodology was created and improved directly during the licensing process. In addition, in accordance with the Energy Strategy of Ukraine up to 2035, one of the key task is the further diversification of nuclear fuel suppliers. Within the framework of the Executive Agreement between the Government of Ukraine and the U.S. Government, activities have been underway since 2000 on the introduction of Westinghouse fuel. The purpose of this project is to develop, supply and qualify alternative nuclear fuel compatible with fuel produced in Russia for Ukrainian NPPs. In addition, a supplementary approach to safety analysis report is being developed to justify feasibility of loading new fuel into the DSFSF containers. The stated results should demonstrate the fulfillment of design criteria under normal operating conditions, abnormal conditions and design-basis accidents of DSFSF components.  Thus, the paper highlights both the main problems of DSFSF licensing and obtaining permission for placing new fuel types in DSFSF.

Long-term safety of the extended SFR - Methodology and conclusions from the SR-PSU project

MRS Advances ◽  
2016 ◽  
Vol 1 (61) ◽  
pp. 4075-4080
Author(s):  
Fredrik Vahlund
Keyword(s):  
Radioactive Waste ◽  
Nuclear Fuel ◽  
Nuclear Power ◽  
Safety Assessment ◽  
Power Plants ◽  
Spent Nuclear Fuel ◽  
Surface System ◽  
Radiological Safety ◽  
The Impact

ABSTRACTSince 1988 the Swedish Nuclear Fuel and Waste Management Co. operates a repository for low- and intermediate-level short-lived radioactive waste, SFR, in Forsmark, Sweden. Due to decommissioning of the nuclear power plants additional storage capacity is needed. In December 2014, an application to extend the repository was therefore submitted. One key component of this application was an assessment of post-closure safety of the extended SFR. For this safety assessment, a methodology based on that developed by SKB for the spent nuclear fuel repository was used and the impact of the degradation of repository components, the evolution of the surface system and changes of future climate on the radiological safety of the repository was assessed over a period of 100,000 years. The central conclusion of the SR-PSU safety assessment is that the extended SFR repository meets requirements on protection of human health and of the environment that have been established by the Swedish radiation safety authority for the final disposal of radioactive waste. Furthermore, the design of the repository was shown suitable for the waste selected and the applied methodology suitable for the safety assessment.

Sorption of Actinides in Well-Defined Oxidation States on Geologic Media

1981 ◽  
Vol 11 ◽  
Author(s):  
B. Allard ◽  
U. Olofsson ◽  
B. Torstenfelt ◽  
H. Kipatsi ◽  
K. Andersson
Keyword(s):  
Nuclear Fuel ◽  
Spent Nuclear Fuel ◽  
Oxidation States ◽  
Spent Fuel ◽  
Long Term Storage ◽  
Term Storage ◽  
Geologic Media

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.

Release of 108Ag from Irradiated PWR Control Rod Absorbers under Deep Repository Conditions

2015 ◽  
Vol 1744 ◽  
pp. 217-222
Author(s):  
O. Roth ◽  
M. Granfors ◽  
A. Puranen ◽  
K. Spahiu
Keyword(s):  
Nuclear Fuel ◽  
Source Term ◽  
Spent Nuclear Fuel ◽  
Nuclear Reactors ◽  
Reactor Irradiation ◽  
Spent Fuel ◽  
Control Rod ◽  
Potential Source ◽  
Absorber Material ◽  
Control Rods

ABSTRACTIn a future Swedish deep repository for spent nuclear fuel, irradiated control rods from PWR nuclear reactors are planned to be stored together with the spent fuel. The control rod absorber consists of an 80% Ag, 5% Cd, 15% In alloy with a steel cladding. Upon in-reactor irradiation 108Ag is produced by neutron capture. Release of 108Ag has been identified as a potential source term for release of radioactive substances from the deep repository.Under reducing deep repository conditions, the Ag corrosion rate is however expected to be low which would imply that the release rate of 108Ag should be low under these conditions. The aim of this study is to investigate the dissolution of PWR control rod absorber material under conditions relevant to a future deep repository for spent nuclear fuel. The experiments include tests using irradiated control rod absorber material from Ringhals 2, Sweden. Furthermore, un-irradiated control rod absorber alloy has been tested for comparison. The experiments indicate that the release of Ag from the alloy when exposed to water is strongly dependent on the redox conditions. Under aerated conditions Ag is released at a significant rate whereas no release could be measured after 133 days during leaching under H2.

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