Published March 31, 2009 | Version v1
Journal article

High level nuclear waste glass corrosion in synthetic clay pore solution and retention of actinides in secondary phases

  • 1. Institut fuer Nukleare Entsorgung (INE), Forschungszentrum Karlsruhe, P.O. Box 3640, 76021 Karlsruhe (Germany)

Description

The corrosion of the simulated high level waste glass GP WAK1 in synthetic clay pore solution was studied in batch-type experiments at 323 and 363 K with special focus on the effect of high carbonate concentration in solution. The corrosion rate after 130 days was <10-4 g m-2 d-1 - no significant effect of the carbonate was identified. During glass corrosion, crystalline secondary phases (powellite, barite, calcite, anhydrite and clay-like Mg(Ca,Fe)-silicates) were formed. To obtain a molecular level picture of radionuclide speciation within the alteration layer, spectroscopic methods have been applied including grazing incidence X-ray absorption spectroscopy (XAS) to study the structural changes in the coordination of uranyl upon alteration layer formation. The number of equatorial oxygen atoms increases from 4 in the bulk glass to 5 in the alteration layer. Furthermore, reduced coordination symmetry was found. Hectorite, a frequently observed secondary clay mineral within the glass alteration layer, was synthesized in the presence of trivalent f-elements (e.g. Eu) and structurally characterized using time-resolved laser fluorescence spectroscopy. Structural incorporation into the octahedral layer is indicated

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jnucmat.2008.12.044

Additional details

Identifiers

DOI
10.1016/j.jnucmat.2008.12.044;
PII
S0022-3115(08)00755-1;

Publishing Information

Journal Title
Journal of Nuclear Materials
Journal Volume
385
Journal Issue
2
Journal Page Range
p. 456-460
ISSN
0022-3115
CODEN
JNUMAM

Conference

Title
3. symposium N on nuclear materials
Acronym
E-MRS 2008 spring meeting
Dates
26-30 May 2008
Place
Strasbourg (France)

Optional Information

Copyright
Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.