The controversial role of inter-diffusion in glass alteration

被引:82
|
作者
Gin, S. [1 ]
Neill, L. [2 ]
Fournier, M. [1 ]
Frugier, P. [1 ]
Ducasse, T. [1 ]
Tribet, M. [1 ]
Abdelouas, A. [3 ]
Parruzot, B. [4 ]
Neeway, J. [4 ]
Wall, N. [2 ]
机构
[1] CEA, DEN, DTCD, SECM, F-30207 Bagnols Sur Ceze, France
[2] Washington State Univ, Dept Chem, Pullman, WA 99164 USA
[3] Univ Nantes, SUBATECH, Ecole Mines Nantes, CNRS,IN2P3,UMR 6457, F-44307 Nantes 3, France
[4] Pacific NW Natl Lab, Energy & Environm Directorate, Richland, WA 99352 USA
关键词
Glass; Alteration; Dissolution; Kinetics; Rate; SON68; Mechanisms; Leaching; Inter-diffusion; NUCLEAR-WASTE GLASS; INTERFACIAL DISSOLUTION-REPRECIPITATION; INTERNATIONAL SIMPLE GLASS; LONG-TERM BEHAVIOR; 50; DEGREES-C; BOROSILICATE GLASS; ALTERATION MECHANISMS; SURFACE-LAYERS; PERFORMANCE ASSESSMENT; SOLUTION CHEMISTRY;
D O I
10.1016/j.chemgeo.2016.07.014
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Current kinetic models for nuclear waste glasses (e.g. GM2001, GRAAL) are based on a set of mechanisms that have been generally agreed upon within the international waste glass community. These mechanisms are: hydration and ion exchange reactions (the two processes are referred as inter-diffusion), hydrolysis of the silicate network, and condensation/precipitation of partly or completely hydrolyzed species that produces a porous and amorphous layer and crystalline phases on surface of the altered glass. Recently, a new idea with origins in the mineral dissolution community has been proposed that excludes inter-diffusion processes as a potential rate limiting mechanism. To understand how the newly,proposed interfacial dissolution/precipitation model can change the current understanding of glass corrosion, a key experiment used to account for this model was replicated to further revisit the interpretation. This experiment was performed far from saturation, at 50 degrees C, with SON68 glass, in static mode, deionized water, and a S/V ratio of 10 m(-1) for 6 months. Results were repeatable and showed that glass dissolution rate progressively dropped by similar to 1 order of magnitude compared to the forward rate, suggesting that a dense surface layer was under construction. According to previous and new solids characterizations, it is concluded that neither a simple inter-diffusion model nor the interfacial dissolution/precipitation model can account for the observed elemental profiles within the alteration layer. More generally, far-from- and close-to-saturation conditions must be distinguished, This argument is bolstered by literature where evidence shows that inter-diffusion takes place in acidic conditions and far from saturation. However, closer to saturation, when a sufficiently dense layer is formed, a new approach is proposed requiring a full description of chemical reactions taking place within the alteration layer and an accurate budget of hydrous species along the profile as it is thought that the access of a sufficient amount of water to the pristine glass is the rate-limiting process in these conditions. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 123
页数:9
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