Glass Surface area to Solution Volume Ratio and its Implications to Accelerated Leach Testing

1982 ◽  
Vol 15 ◽  
Author(s):  
Larry R. Pederson ◽  
Charles Q. Buckwalter ◽  
Gary L. Mcvay ◽  
B. Lynn Riddle

ABSTRACTLeaching tests of PNL 76–68 glass in deionized water have been performed using the standard MCC-l static leaching procedure but with varied glass surface area to solution volume ratios (SA/V). It was found that leaching could be strongly influenced by the SA/V ratio, due largely to an effect of silicon solubility limitations. The conclusion that solubility and not solid state diffusion is most important in regulating leaching rates is supported by (1) the similarities in depth profiles of all soluble glass components with none depleted to depths greater than that of silicon despite vastly different solid state diffusivities, and (2) the lack of dependence of leaching rates on reaction layer thicknesses. To more directly examine the influence of dissolved silicon on glass leaching rates, leaching tests were performed in silicic acid solutions and in two actual groundwaters. As expected, leaching rates of all soluble glass components were reduced by amounts roughly proportional to the silicon saturation fraction. Since solubility modifies leaching rates in all but very dilute solutions, short-term tests at high SA/V values can be used to predict solution concentrations for long-term tests at low SA/V values, although reaction layers formed are not of the same thickness. Glass leaching data for a range of leaching times and SA/V values can be represented by a single curve when plotted versus the product of SA/V and time. However, the use of SA/V variations may have limited usefulness in accelerated leach testing for multicomponent systems. Events such as silica colloid and certain alteration phase formations modify the above relationship.

1982 ◽  
Vol 15 ◽  
Author(s):  
Albert J. Machiels ◽  
Claudio Pescatore

ABSTRACTThe effects of the surface area-to-solution volume ratio on waste glass leach rates are investigated from a theoretical point of view. Simple leach models are discussed first. Correlation variables to interpret the results of similar leaching experiments performed at different values of the surface area-to-solution volume ratio are obtained for static leach testing. For dynamic leaching conditions, the source term required for risk assessment is derived and its dependence on the leachant flow rate and leach specimen surface area is discussed. The findings are upheld by a more complex leach model, the mathematical formulation of which has been implemented in a computer code named LIX. When tested against actual PNL 76–68 glass leaching data, LIX shows excellent capabilities in reproducing the experimental evidence, in particular the effects of the surface area-to-solution volume ratio.


1983 ◽  
Vol 62 (2) ◽  
pp. 151-158 ◽  
Author(s):  
L. R. Pederson ◽  
C. Q. Buckwalter ◽  
G. L. McVay

2008 ◽  
Vol 39-40 ◽  
pp. 279-286 ◽  
Author(s):  
Pavel Šlemín ◽  
Gerhard Heide ◽  
Aleš Helebrant

Both the static and dynamic corrosion tests of E-glass were used for different conditions - temperature, glass surface to solution volume ratio (S/V), solution flow rate (F) and F/S ratio. Results obtained for glass fibres were compared with the ones for glass grains and planar samples. Evaluation of experimental results by kinetic model shows that the change of glass surface should be taken into account in the case of fibres corrosion. The total incongruent process of dissolution could be explained as congruent dissolution of glass accompanied by back precipitation of SiO2 or silicates. In most cases, more then 90% of SiO2 precipitates back. The second possible explanation, i.e. SiO2 network dissolution accompanied by selective leaching of Ca, B and Al, is not very probable. The glass sample shape can influence the estimation of dissolution rate. Up to now, with existing kinetic models, the dissolution rates evaluated from experiments with different shapes of glass (fibres, grains, planar) cannot be used as materials properties.


1994 ◽  
Vol 66-67 (s1) ◽  
Author(s):  
James D. Prikryl ◽  
Roberto T. Pabalan ◽  
David R. Turner ◽  
Bret W. Leslie

1989 ◽  
Vol 176 ◽  
Author(s):  
X. Feng ◽  
I. L. Pegg ◽  
Y. Guo ◽  
AA. Barkatt ◽  
P. B. Macedo

ABSTRACTWe report data on the relationship between nuclear waste glass durability, as measured by leachate concentrations and leach rates, and the ratio of glass surface area to solution volume, S/V. The study includes West Valley non-radioactive production glasses (SF6 and SF10), West Valley glasses containing U and Th designed at CUA (WVCM47, WVCM50, and WVCM59), Savannah River SRLTDS-131 glass, and Hanford waste glass HW-39 (for which existing literature data is used). While some of these glasses show departures of leachate concentrations from simple (S/V)t scaling others conform well. The departures are, in all cases, most evident at high values of S/V. It is therefore important, therefore to understand how glass composition determines which corrosion mechanism is dominant in order to assess the region of validity of extrapolations based on (S/V)t scaling. While leach rates show a general tendency to decrease with S/V and time, exceptions are evident for the less durable glasses which show minima and maxima in the S/V-dependence at fixed time.


2000 ◽  
Vol 663 ◽  
Author(s):  
M. Lobanova ◽  
L. Maurer ◽  
P. Barboux ◽  
F. Devreux ◽  
Y. Minet

ABSTRACTOne presents the results of numerical simulations of glass leaching. The glass is modelled as a random mixture of partly and totally soluble species, which represent silica, and boron or alkali oxides, respectively. It is shown that the dissolution rate and the thickness of the altered surface layer are strongly dependent on the glass composition, whereas the equilibrium solubility is not. The dependence of the layer thickness on the glass surface area to solution volume ratio is also emphasized. The protective role of the surface layer is shown to arise from its restructuring after the extraction of the soluble species. The simulation results are compared to an experimental study performed on series of SiO2-B2O3-Na2O glasses.


1996 ◽  
Vol 465 ◽  
Author(s):  
J. Wei ◽  
P. Van Iseghem

ABSTRACTDuring the reaction of HLW glass with interstitial clay water at different temperatures with various ratios of glass surface area to solution volume (SA/V) and durations, Eu released from the glass forms predominantly Eu-humate colloids (organic colloids) by a complexation reaction. The size distribution and stability of Eu-humate colloids have been characterized. It is likely that inorganic colloids which are mainly composed of Si, Al and Ca are generated from the corrosion of waste glass by a nucleation reaction.


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