Abstract
ABSTRACTWe have characterized the corrosion behavior of several Defense Waste
Processing Facility (DWPF) reference waste glasses by conducting static
dissolution tests with crushed glasses. Glass dissolution rates were
calculated from measured B concentrations in tests conducted for up to five
years. The dissolution rates of all glasses increased significantly after
certain alteration phases precipitated. Calculation of the dissolution rates
was complicated by the decrease in the available surface area as the glass
dissolves. We took the loss of surface area into account by modeling the
particles to be spheres, then extracting from the short-term test results
the dissolution rate corresponding to a linear decrease in the radius of
spherical particles. The measured extent of dissolution in tests conducted
for longer times was less than predicted with this linear dissolution model.
This indicates that advanced stages of corrosion are affected by another
process besides dissolution, which we believe to be associated with a
decrease in the precipitation rate of the alteration phases. These results
show that the dissolution rate measured soon after the formation of certain
alteration phases provides an upper limit for the long-term dissolution
rate, and can be used to determine a bounding value for the source term for
radionuclide release from waste glasses. The long-term dissolution rates
measured in tests at 20,000 m−1 at 90°C in tuff groundwater at pH
values near 12 are about 0.2,0.07, and 0.04 g/(m2•d) for the
Environmental Assessment glass and glasses made with SRL 131 and SRL 202
frits, respectively.
Publisher
Springer Science and Business Media LLC
Cited by
8 articles.
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