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.

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 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.

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.

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.

Operational Model for the Spent Nuclear Fuel Radionuclides Source Term in Presence of Water

2001 ◽  
Author(s):  
Christophe Poinssot ◽  
Christophe Jegou ◽  
Pierre Toulhoat ◽  
Jean-Marie Gras
Keyword(s):  
Nuclear Fuel ◽  
Closed System ◽  
Source Term ◽  
Spent Nuclear Fuel ◽  
Driving Forces ◽  
Spent Fuel ◽  
Microscopic Description ◽  
Operational Model ◽  
Geological Disposal ◽  
Source Term Model

Abstract Under the geological disposal conditions, spent fuel (SF) is expected to evolve during the 10,000 years while being maintained isolated from the biosphere before water comes in. Under those circumstances, several driving forces would lead to the progressive intrinsic transformations within the rod which would modify the subsequent release of radionuclides: the production of a significant volume of He, the accumulation of irradiation defects, the slow migration of radionuclides (RN) within the pellet. However, the current RN source terms for SF never accounted for these evolutions and was based on the existing knowledge on the fresh SF. Two major mechanisms were considered, the leaching of the readily available fraction (one which was supposed to be instantly accessible to water), and the release of RN through alteration of the UO2 grains. We are now proposing a new RN source term model based on a microscopic description of the system in order to also account for the early evolution of the closed system, the amplitude of which increases with the burnup and is greater for MOX fuels.

Chemical Effects at the Reaction Front in Corroding Spent Nuclear Fuel

2006 ◽  
Vol 985 ◽  
Author(s):  
Jeffrey A. Fortner ◽  
A. Jeremy Kropf ◽  
James L. Jerden ◽  
James C. Cunnane
Keyword(s):  
Transition Zone ◽  
Nuclear Fuel ◽  
Spent Nuclear Fuel ◽  
Aqueous Environment ◽  
Spent Fuel ◽  
Aqueous Corrosion ◽  
Reduction Potentials ◽  
Chemical Effects ◽  
Before And After ◽  
X Ray Absorption

AbstractPerformance assessment models of the U. S. repository at Yucca Mountain, Nevada suggest that neptunium from spent nuclear fuel is a potentially important dose contributor. A scientific understanding of how the UO2 matrix of spent nuclear fuel impacts the oxidative dissolution and reductive precipitation of Np is needed to predict the behavior of Np at the fuel surface during aqueous corrosion. Neptunium would most likely be transported as aqueous Np(V) species, but for this to occur it must first be oxidized from the Np(IV) state found within the parent spent nuclear fuel. In this paper we present synchrotron x-ray absorption spectroscopy and microscopy findings that illuminate the resultant local chemistry of neptunium and plutonium within uranium oxide spent nuclear fuel before and after corrosive alteration in an air-saturated aqueous environment. We find the Pu and Np in unaltered spent fuel to have a +4 oxidation state and an environment consistent with solid-solution in the UO2 matrix. During corrosion in an air-saturated aqueous environment, the uranium matrix is converted to uranyl (UO22+) mineral assemblage that is depleted in Np and Pu relative to the parent fuel. The transition from U(IV) in the fuel to a fully U(VI) character across the corrosion front is not sharp, but occurs over a transition zone of ∼ 50 micrometers. We find evidence of a thin (∼ 20 micrometer) layer that is enriched in Pu and Np within a predominantly U(IV) environment on the fuel side of the transition zone. These experimental observations are consistent with available data for the standard reduction potentials for NpO2+/Np4+ and UO22+/U4+ couples, which indicate that Np(IV) may not be effectively oxidized to Np(V) at the corrosion potential of uranium dioxide spent nuclear fuel in air-saturated aqueous solutions.

scholarly journals The Need for Integrating the Back End of the Nuclear Fuel Cycle in the United States of America

MRS Advances ◽  
2018 ◽  
Vol 3 (19) ◽  
pp. 991-1003 ◽  
Author(s):  
Evaristo J. Bonano ◽  
Elena A. Kalinina ◽  
Peter N. Swift
Keyword(s):  
United States ◽  
Nuclear Fuel ◽  
United States Of America ◽  
Spent Nuclear Fuel ◽  
Fuel Cycle ◽  
Nuclear Fuel Cycle ◽  
The United States ◽  
Spent Fuel ◽  
Dry Storage ◽  
The Us

ABSTRACTCurrent practice for commercial spent nuclear fuel management in the United States of America (US) includes storage of spent fuel in both pools and dry storage cask systems at nuclear power plants. Most storage pools are filled to their operational capacity, and management of the approximately 2,200 metric tons of spent fuel newly discharged each year requires transferring older and cooler fuel from pools into dry storage. In the absence of a repository that can accept spent fuel for permanent disposal, projections indicate that the US will have approximately 134,000 metric tons of spent fuel in dry storage by mid-century when the last plants in the current reactor fleet are decommissioned. Current designs for storage systems rely on large dual-purpose (storage and transportation) canisters that are not optimized for disposal. Various options exist in the US for improving integration of management practices across the entire back end of the nuclear fuel cycle.

The SR 97 Safety Assessment of a KBS 3 Repository for Spent Nuclear Fuel – Overview, Review Comments and New Developments

2002 ◽  
Vol 713 ◽  
Author(s):  
Allan Hedin ◽  
Ulrik Kautsky ◽  
Lena Morén ◽  
Patrik Sellin ◽  
Jan-Olof Selroos
Keyword(s):  
Nuclear Fuel ◽  
Safety Assessment ◽  
Spent Nuclear Fuel ◽  
Bentonite Clay ◽  
Research Programme ◽  
High Strength ◽  
Functional Requirements ◽  
Future Evolution ◽  
Site Investigations ◽  
Potential Safety

ABSTRACTIn preparation for coming site investigations for siting of a deep repository for spent nuclear fuel, the Swedish Nuclear Fuel and Waste Management Company, SKB has carried out the longterm safety assessment SR 97, requested by the Swedish Government. The repository is of the KBS-3 type, where the fuel is placed in isolating copper canisters with a high-strength cast iron insert. The canisters are surrounded by bentonite clay in individual deposition holes at a depth of 500 m in granitic bedrock. Geological data are taken from three sites in Sweden to shed light on different conditions in Swedish granitic bedrock.The future evolution of the repository system is analysed in the form of five scenarios. The first is a base scenario where the repository is postulated to be built entirely according to specifications and where present-day conditions in the surroundings, including climate, persist. The four other scenarios show the evolution if the repository contains a few initially defective canisters, in the event of climate change, in the event of earthquakes, and in the event of future inadvertent human intrusion.The principal conclusion of the assessment is that the prospects of building a safe deep repository for spent nuclear fuel in Swedish granitic bedrock are very good. The results of the assessment also serve as a basis for formulating requirements and preferences regarding the bedrock in site investigations, for designing a programme for site investigations, for formulating functional requirements on the repository's barriers, and for prioritisation of research.SR 97 has been reviewed both by an international group of OECD/NEA experts and by Swedish authorities. The NEA reviewers concluded that “SR 97 provides a sensible illustration of the potential safety of the KBS-3 concept”, and no issues were identified that need to be resolved prior to proceeding to the investigation of potential sites. The authorities' conclusions were in principal consistent with those of the NEA.Uncertainties and lack of knowledge in different areas identified in SR 97 have strongly influenced the contents and structure of SKBs most recent research programme, RD&DProgramme 2001.Since SR 97, the methodology for probabilistic consequence analyses have been further developed. Analytic approximations to the numerical transport models used in SR 97 have been developed. The new models have been used to extend the probabilistic calculations in SR 97.

scholarly journals Thermal Ionization-Isotope Dilution Mass Spectrometry Determination of Ruthenium in Spent Nuclear Fuel

2013 ◽  
Vol 25 (12) ◽  
pp. 7044-7046 ◽  
Author(s):  
Young-Shin Jeon ◽  
Yang-Soon Park ◽  
Jung-Suk Kim ◽  
Sun-Ho Han ◽  
Yong Joon Park
Keyword(s):  
Mass Spectrometry ◽  
Nuclear Fuel ◽  
Isotope Dilution ◽  
Spent Nuclear Fuel ◽  
Isotope Dilution Mass Spectrometry ◽  
Thermal Ionization
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