The Long-Term Corrosion and Modelling of Two Simulated Belgian Reference High-Level Waste Glasses

1987 ◽  
Vol 112 ◽  
Author(s):  
P. Van Iseghem ◽  
B. Grambow

AbstractThe corrosion behaviour in distilled water of two simulated candidate high level waste borosilicate glasses (SAN602519L3C2 and SM58LW11) his been investigated at 90°C for different SA/V condition's 10, 100, 7800 m−1). The experimental data were modelled using the PHREEQE and GLASSOL computer codes. The model is quite successful for describing the corrosion behaviour, using experimentally derived values for the forward rate, silica saturation and the final rate. GWss SAN60 is more stable than glass SM58 at SA/V values of 10 and 100 m−1, but in the long term the relative performance is inverse. Indeed, the high Al content of SAN60 induces the creation of analcime crystals after SiO2 has reached its saturation concentration in solution, which cause an enhancement of the final rate of dissolution of the glass; for SM58 on the contrary the SiO2 solution is a stable condition.

1981 ◽  
Vol 6 ◽  
Author(s):  
Richard G. Strickert ◽  
Dhanpat Rai

ABSTRACTKnowledge of Pu solid phases present in nuclear wastes is important for predicting the geochemical behavior of Pu. Thermodynamic data and experimental measurements using discrete Pu compounds, Pu-doped borosilicate glasses (simulating a high-level waste form), and Pu contaminated sediments suggest that PuO2(c) is very stable and is expected to be present in the repository. The solubility of the stable phase, such as PuO2(c), can be used to predict the maximum Pu concentration in solutions for long-term safety assessment of nuclear waste repositories.


1988 ◽  
Vol 127 ◽  
Author(s):  
J. P. Simpson ◽  
R. Schenk

ABSTRACTHydrogen evolution from anoxic corrosion of cast steel overpacks in high-level waste repositories is an important issue for design if, as has been estimated, the hydrogen is prevented from escaping by diffusion by a low permeability compacted bentonite backfill.Evaluation of the corrosion results showed three basic types of corrosion behaviour: general corrosion with oxide layer formation, unstable corrosion behaviour with pitting or macro-element formation and stable passive behaviour.Cast steel containers under Swiss repository conditions are expected to suffer general corrosion with oxide layer formation. This behaviour gives the highest long term corrosion rates (2–5 μm/a) without local attack, above the 0.03–0.8 μm/a tolerated for hydrogen escape by diffusion but below the 20 μm/a assumed for overpack design.


Author(s):  
Bruno Kursten ◽  
Frank Druyts ◽  
Pierre Van Iseghem

Abstract The current worldwide trend for the final disposal of conditioned high-level, medium-level and long-lived alpha-bearing radioactive waste focuses on deep geological disposal. During the geological disposal, the isolation between the radioactive waste and the environment (biosphere) is realised by the multibarrier principle, which is based on the complementary nature of the various natural and engineered barriers. One of the main engineered barriers is the metallic container (overpack) that encloses the conditioned waste. In Belgium, the Boom Clay sediment is being studied as a potential host rock formation for the final disposal of conditioned high-level radioactive waste (HLW) and spent fuel. Since the mid 1980’s, SCK•CEN has developed an extensive research programme aimed at evaluating the suitability of a wide variety of metallic materials as candidate overpack material for the disposal of HLW. A multiple experimental approach is applied consisting of i) in situ corrosion experiments, ii) electrochemical experiments (cyclic potentiodynamic polarisation measurements and monitoring the evolution of ECORR as a function of time), and iii) immersion experiments. The in situ corrosion experiments were performed in the underground research facility, the High Activity Disposal Experimental Site, or HADES, located in the Boom clay layer at a depth of 225 metres below ground level. These experiments aimed at predicting the long-term corrosion behaviour of various candidate container materials. It was believed that this could be realised by investigating the medium-term interactions between the container materials and the host formation. These experiments resulted in a change of reasoning at the national authorities concerning the choice of over-pack material from the corrosion-allowance material carbon steel towards corrosion-resistant materials such as stainless steels. The main arguments being the severe pitting corrosion during the aerobic period and the large amount of hydrogen gas generated during the subsequent anaerobic period. The in situ corrosion experiments however, did not allow to unequivocally quantify the corrosion of the various investigated candidate overpack materials. The main shortcoming was that they did not allow to experimentally separate the aerobic and anaerobic phase. This resulted in the elaboration of a new laboratory programme. Electrochemical corrosion experiments were designed to investigate the effect of a wide variety of parameters on the localised corrosion behaviour of candidate overpack materials: temperature, SO42−, Cl−, S2O32−, oxygen content (aerobic - anaerobic),… Three characteristic potentials can be derived from the cyclic potentiodynamic polarisation (CPP) curves: i) the open circuit potential, OCP, ii) the critical potential for pit nucleation, ENP, and iii) the protection potential, EPP. Monitoring the open circuit potential as a function of time in clay slurries, representative for the underground environment, provides us with a more reliable value for the corrosion potential, ECORR, under disposal conditions. The long-term corrosion behaviour of the candidate overpack materials can be established by comparing the value of ECORR relative to ENP and EPP (determined from the CPP-curves). The immersion tests were developed to complement the in situ experiments. These experiments aimed at determining the corrosion rate and to identify the corrosion processes that can occur during the aerobic and anaerobic period of the geological disposal. Also, some experiments were elaborated to study the effect of graphite on the corrosion behaviour of the candidate overpack materials.


2019 ◽  
Vol 2019 ◽  
pp. 1-10
Author(s):  
Hailin Yang ◽  
Mingjiao Fu ◽  
Bobo Wu ◽  
Ying Zhang ◽  
Ruhua Ma ◽  
...  

For the proposed novel procedure of immobilizing HLW with magnesium potassium phosphate cement (MKPC), Fe2O3 was added as a modifying agent to verify its effect on the solidification form and the immobilization of the radioactive nuclide. The results show that Fe2O3 is inert during the hydration reaction. It slows down the hydration reaction and lowers the heat release rate of the MKPC system, leading to a 3°C-5°C drop in the mixture temperature during hydration. Early comprehensive strength of Fe2O3 containing samples decreased slightly while the long-term strength remained unchanged. For the sintering process, Fe2O3 played a positive role, lowering the melting point and aiding the formation of ceramic structure. CsFe(PO4)2, or CsFePO4, was generated by sintering at 900°C. These products together with the ceramic structure and absorption benefit the immobilization of Cs+. The optimal sintering temperature for heat treatment is 900°C; it makes the solidification form a fired ceramic-like structure.


1998 ◽  
Vol 124 (1) ◽  
pp. 88-100 ◽  
Author(s):  
James L. Conca ◽  
Michael J. Apted ◽  
Wei Zhou ◽  
Randolph C. Arthur ◽  
John H. Kessler

1981 ◽  
Vol 11 ◽  
Author(s):  
T. J. Headley ◽  
G. W. Arnold ◽  
C. J. M. Northrup

The long-term stability of nuclear waste forms is an important consideration in their selection for safe disposal of radioactive waste. Stability against long-term radiation damage is particularly difficult to assess by short-term laboratory experiments. Much of the displacement damage in high-level waste forms will be generated by heavy recoil nuclei emitted during the α-decay process of long-lived actinide elements. Hence, an accelerated aging test which reliably simulates the α-recoil damage accumulated during thousands of years of storage is desirable. One recent approach to this simulation is to implant the waste form with heavy Pb-ions.I- 6 If the validity of this approach is to be fully assessed, two important questions which have not yet been investigated must be answered.(1) Is the structural damage, including cumulative effects, similar for irradiation by Pb-ions and a-recoil nuclei in a given material? (2) Is the dose-dependence of the accumulated damage similar? The purpose of this investigation was to assess the extent of these similarities in selected materials. We utilized transmission electron microscopy (TEM) to characterize the radiation damage and measure its dose-dependence.


Author(s):  
A. Meleshyn ◽  
U. Noseck

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.


1984 ◽  
Vol 44 ◽  
Author(s):  
Eberhard Freude ◽  
Bernd Grambow ◽  
Werner Lutze ◽  
Harald Rabe ◽  
Rodney C. Ewing

During the past ten years extensive data have been determined for the corrosion of nuclear waste forms in short-term laboratory experiments (usually less than one year). The long-term behavior of glass has been inferred by: (1) the acceleration of corrosion rates at high temperatures [1]; (2) the use of high surface areas of the glass to small volumes of solution [1]; and the analysis of natural glasses altered over long periods of geologic time [2, 3]. The most recent efforts have concentrated on understanding the mechanisms of corrosion [1, 4, 5]. The corrosion mechanism may be used to make long-term extrapolations of the “stability” of the waste form. In this paper, we consider a linear time dependence for the corrosion under near saturation conditions and use a rate equation in the QTERM code [6, 7, 8] to model the long-term behavior of the German glass, C-31−3EC [9], JSS A [10, 11] and SRL TDS 131 [1]. The data base for C-31−3EC has been published elsewhere [9, 12, 13, 14], and we include experimental work completed by Rabe for boron and silica, at 200°C.


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