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Modeling of radionuclide transport through repository components using finite volume finite element and multidomain methods

机译:使用有限体积有限元和多域方法对通过存储库组件的放射性核素传输进行建模

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This paper presents 3D saturated flow and transport calculations performed using numerical methods developed within the MELODIE software in the framework of assessing the performance of a radioactive waste geological repository. This type of computational modeling is a challenging task due to the presence of strong physical, chemical and hydrogeological heterogeneities, as well as the very different geometrical scales (from dm to km) to be handled simultaneously. First, the software is briefly described, with a particular focus on the specific features that help for dealing with such contrasted system, notably the finite volume finite element and the Schwarz domain decomposition methods. IRSN calculations based on the French "spent fuel/iron canister/clay" concept designed by Andra in the framework of its feasibility study of a deep geological repository are then presented. Through sensitivity analyses based on various evolution scenarios, these calculations aim at assessing the possible influence of design features, waste degradation mechanisms or radionuclide transfer properties of repository components on the behavior of the containment system as a whole. The results of the simulation have shown the transport regime in the drifts depends on the efficiency of the seals. When seals are efficient, velocities are low and transfer regime in the drifts is dominated by diffusion, whereas advection is dominant when seals are poorly sealed. However, whatever the dominant transport regime (diffusion or advection) in the drifts, the activity released out from the canisters was shown to be mainly transferred by diffusion to the host rock exits. This transfer through clayey components (bentonite and host rock) highlights the importance of chemical properties of the three types of long-lived radionuclides considered in the present study. The sensitivity analysis has shown that strongly sorbed and/or weakly soluble radionuclides are less influenced by activity release mechanisms and by seal efficiency. Concerning the strongly sorbed radionuclide Nb-94, the activity is hardly transferred beyond the vicinity of the disposal cells: the sorption properties allow limiting and delaying efficiently radionuclide migration. Concerning the weakly soluble radionuclide Se-79, a part of the activity is instantaneously precipitated in the bentonite surrounding the canisters and the activity release in the system is controlled by the dissolution of this precipitated activity. Such radionuclides are thus hardly concerned with canister dissolution mechanisms. On the contrary, the migration and release at the host rock exits of I-129, which is a non-sorbed and soluble radionuclide, is shown to be influenced by the radionuclide source term, i.e. dissolution mechanism and instantaneous released fraction (IRF). The IRF, which corresponds to 8% of the total activity contained in the canisters impacts significantly the activity released out of the host rock when UO2 matrix dissolution controlled by uranium solubility lasts up to several million years, whereas its contribution is far less marked when matrix dissolves rapidly by alpha-radiolysis.
机译:本文介绍了使用MELODIE软件开发的数值方法在评估放射性废物地质处置库性能的框架中进行的3D饱和流量和输运计算。由于存在强烈的物理,化学和水文地质异质性,并且要同时处理的几何尺寸(从dm到km)非常不同,因此这种类型的计算建模是一项艰巨的任务。首先,简要介绍该软件,特别关注有助于处理这种对比系统的特定功能,特别是有限体积有限元和Schwarz域分解方法。然后介绍了基于安德拉在深部地质库可行性研究框架内设计的法国“废燃料/铁罐/粘土”概念的IRSN计算。通过基于各种演化方案的敏感性分析,这些计算旨在评估存储库组件的设计特征,废物降解机制或放射性核素转移特性对整个收容系统行为的可能影响。仿真结果表明,漂移中的运输方式取决于密封件的效率。当海豹有效时,速度低,漂移中的转移方式主要由扩散引起,而当海豹密封性差时,对流占主导地位。但是,无论漂移中占主导地位的运输方式(扩散或对流),从罐中释放出来的活动都主要是通过扩散转移到主岩出口。通过粘土成分(膨润土和基质岩)的这种转移突出了本研究中考虑的三种长寿命放射性核素化学性质的重要性。敏感性分析表明,强吸附和/或微溶的放射性核素受活性释放机制和密封效率的影响较小。关于强烈吸附的放射性核素Nb-94,其活性很难转移到处置池附近:吸附特性可以限制和延迟有效的放射性核素迁移。关于弱溶性放射性核素Se-79,一部分活性在罐周围的膨润土中立即沉淀,并且该沉淀活性的溶解控制了系统中的活性释放。因此,这种放射性核素几乎与罐的溶解机理无关。相反,I-129是一种非吸附和可溶的放射性核素,在其岩体出口处的迁移和释放受放射性核素来源项(即溶出机理和瞬时释放分数(IRF))的影响。当铀溶解度控制的UO2基质溶解持续数百万年时,IRF相当于碳罐中所含总活性的8%,会显着影响从岩体中释放出的活性,而当基质溶解时,UO2的贡献远不那么明显通过α-放射分解迅速溶解。

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