Modelling The Alteration of Son-68 Glass with Nearfield Materials

2006 ◽  
Vol 932 ◽  
Author(s):  
G. de Combarieu ◽  
P. Barboux ◽  
N. Godon ◽  
Y. Minet ◽  
S. Gin

ABSTRACTThe model tested in this paper couples glass dissolution rate and geochemistry in the surrounding environment, thus leading to the comprehensive description of the interactions between the glass and the minerals and their transformations. Leaching of glass is simulated at 90°C and S/V=80 cm-1 in pure water or with iron from the canister and overpack or with argillite. The glass dissolution is described with an affinity law with respect to a nontronite-like phase, which saturation state depends on Si, Al, Fe, Na and Ca activities. The simulations results allow to reproduce both the decrease of the initial alteration rate and the so-called residual regime while the composition of the alteration layers are explained in terms of precipitated phases. In presence of metallic iron, the corrosion does not affect much glass dissolution rate if silica sorption is neglected. On the contrary, in presence of argillite, the alteration is enhanced by the dissolution of primary clay minerals and the precipitation of feldspar, K-zeolite and clay minerals.

1991 ◽  
Vol 257 ◽  
Author(s):  
H.U. Zwicky ◽  
TH. Graber ◽  
R. Grauer ◽  
R. Restani

ABSTRACTThe dissolution behaviour of two alkali borosilicate glasses has been investigated at 90°C in the presence of potential corrosion inhibitors. The added materials were selected on the basis of surface chemistry considerations: Since the dissolution rate of silicate solid phases in alkaline solutions increases with growing negative surface charge, it should be expected that sorbing cations reduce the reaction rates. Due to the formation of insoluble hydroxides and silicates and to the dominance of neutral or negatively charged hydroxo complexes in the pH range of interest, the selection of potential inhibitors is very restricted.The precipitated hydroxides of Al, Zn, Cd and Pb were chosen as the solid phases. Compared with the experiments in pure water, glass dissolution is enhanced in presence of Al(OH)3 and Zn(OH)2. The concentration of the aqua ions is too low for an inhibiting effect. Sorption of silicic acid on the hydroxide accelerates the glass dissolution. Addition of PbO had a strong inhibiting effect in a 28 days experiment. At longer times an insoluble lead silicate is formed and thereby the glass dissolution rate is increased. Cd on the other hand is still effective as an inhibitor after 365 days.Based on the present results, the possibility of using glass corrosion inhibitors in a repository is considered not to be worthwhile.


1993 ◽  
Vol 333 ◽  
Author(s):  
William L. Bourcier ◽  
Susan A. Carroll ◽  
Brian L. Phillips

ABSTRACTPredictions of long-term glass dissolution rates are highly dependent on the form of the affinity term in the rate expression. Analysis of the quantitative effect of saturation state on glass dissolution rate for CSG glass (a simple analog of SRL-165 glass), shows that a simple (1-Q/K) affinity term does not match experimental results. Our data at 100°C show that the data is better fit by an affinity term having the form where σ =10.


2021 ◽  
Vol 5 (1) ◽  
Author(s):  
C. Carriere ◽  
P. Dillmann ◽  
S. Gin ◽  
D. Neff ◽  
L. Gentaz ◽  
...  

AbstractThe French concept developed to dispose high-level radioactive waste in geological repository relies on glassy waste forms, isolated from the claystone host rock by steel containers. Understanding interactions between glass and surrounding materials is key for assessing the performance of a such system. Here, isotopically tagged SON68 glass, steel and claystone were studied through an integrated mockup conducted at 50 °C for 2.5 years. Post-mortem analyses were performed from nanometric to millimetric scales using TEM, STXM, ToF-SIMS and SEM techniques. The glass alteration layer consisted of a crystallized Fe-rich smectite mineral, close to nontronite, supporting a dissolution/reprecipitation controlling mechanism for glass alteration. The mean glass dissolution rate ranged between 1.6 × 10−2 g m−2 d−1 to 3.0 × 10−2 g m−2 d−1, a value only 3–5 times lower than the initial dissolution rate. Thermodynamic calculations highlighted a competition between nontronite and protective gel, explaining why in the present conditions the formation of a protective layer is prevented.


Author(s):  
Karel Lemmens ◽  
Marc Aertsens ◽  
Ve´ra Pirlet ◽  
Norbert Maes ◽  
Hugo Moors ◽  
...  

To estimate the lifetime of vitrified high level waste (HLW-glass) in Boom Clay disposal conditions, the dissolution behaviour of waste glass has been studied with experiments performed in surface laboratories and in the HADES underground research facility of SCK·CEN since 1980. We present the main topics and first results of the SCK·CEN programme 2000–2003. This programme focuses on the following items: (1) the diffusion/sorption/precipitation of silica in Boom clay or backfill clay, (2) demonstration of glass dissolution behaviour in realistic test conditions, (3) the effect of presaturation of the clay with silica, and (4) the estimation of near field concentrations of critical isotopes. The experiments have shown so far that Si, released by the glass, is effectively immobilized by Boom Clay, but it can nevertheless diffuse into the clay without immediately precipitating. The dissolution rate of glass SON68 and SM539 is determined in Boom Clay at in situ density and at 30°C (this is the long-term temperature expected near the waste glass packages in a Boom Clay repository). The dissolution rates, based on glass mass losses, are constant during the first year, at ∼ 0.010 g.m−2.day−1 for glass SON68 and ∼ 0.012 g.m−2.day−1 for glass SM539. The addition of glass frit causes a decrease of the glass dissolution rate, both with glass SON68 and SM539, and both in Boom Clay and in FoCa-clay. In FoCa-clay at high density with glass frit, the dissolution rates, based on glass mass losses, after 8 months at 30°C are ∼ 0.001 g.m−2.day−1 (SM539) and ∼0.005 g.m−2.day−1 (SON68). Because the experiments performed in Boom Clay and FoCa-clay with glass frit simulate realistic conditions (high clay density, low temperature), they can be used to estimate the maximum glass dissolution rate in a (Boom) clay repository. The corresponding minimum lifetime of a glass canister, calculated with the SCK·CEN code for lifetime predictions, is of the order of 105 to 106 years, if we neglect the internal glass surface area (due to cracking). In more diluted clay suspensions with glass frit, the glass dissolution rate is 10−4 to 10−5 g.m−2.day−1 or even zero. This would correspond to a lifetime of >>106 years. So far, there is no indication that the addition of glass frit leads to secondary phase formation at low temperature (30–40°C). Leach experiments with doped glasses SON68 and SM539 suggest that the maximum concentrations of most critical radionuclides in near field conditions are lower than the best estimate solubilities used for performance assessment studies in Boom Clay. For Se, relatively high concentrations were measured, though. The research programme for the underground laboratory is not discussed.


Author(s):  
Tomohiro Furukawa ◽  
Yasushi Hirakawa

As a preliminary investigation into the establishment of a lithium removal technique for the components used at the International Fusion Materials Irradiation Facility (IFMIF), experiments were performed on the dissolution of lithium in three solvents: ethanol, pure water, and ethanol–water. In these experiments, hemispherical lithium was immersed in the solvents at constant temperatures, and the degree of dissolution was measured continuously from the height of the sample. From the obtained data, the average dissolution rate in the solvents at each testing temperature (10–90 °C) and the amount of hydrogen generated by the chemical reaction were calculated. The average dissolution rates in ethanol, pure water, and ethanol–water at 30 °C were 0.01, 1.6, and 0.43 mm/min, respectively. Although the average dissolution rate increased with the testing temperature in the low-temperature range (10–50 °C) for all solvents, this increase was saturated in the high-temperature range (50–90 °C) in experiments with pure water and ethanol–water as solvents. The volume of gas collected during each experiment was in good agreement with the volume of hydrogen assumed to be generated from the chemical reaction of lithium with the solvents.


2012 ◽  
Vol 12 (13) ◽  
pp. 5859-5878 ◽  
Author(s):  
V. Pinti ◽  
C. Marcolli ◽  
B. Zobrist ◽  
C. R. Hoyle ◽  
T. Peter

Abstract. Emulsion and bulk freezing experiments were performed to investigate immersion ice nucleation on clay minerals in pure water, using various kaolinites, montmorillonites, illites as well as natural dust from the Hoggar Mountains in the Saharan region. Differential scanning calorimeter measurements were performed on three different kaolinites (KGa-1b, KGa-2 and K-SA), two illites (Illite NX and Illite SE) and four natural and acid-treated montmorillonites (SWy-2, STx-1b, KSF and K-10). The emulsion experiments provide information on the average freezing behaviour characterized by the average nucleation sites. These experiments revealed one to sometimes two distinct heterogeneous freezing peaks, which suggest the presence of a low number of qualitatively distinct average nucleation site classes. We refer to the peak at the lowest temperature as "standard peak" and to the one occurring in only some clay mineral types at higher temperatures as "special peak". Conversely, freezing in bulk samples is not initiated by the average nucleation sites, but by a very low number of "best sites". The kaolinites and montmorillonites showed quite narrow standard peaks with onset temperatures 238 K


1989 ◽  
Vol 176 ◽  
Author(s):  
Kevin G. Knauss ◽  
William L. Bourcier ◽  
Kevin D. McKeegan ◽  
Celia I. Merzbacher ◽  
Son N. Nguyen ◽  
...  

ABSTRACTWe have measured the dissolution rate of a simple five-component borosilicate glass (Na2O, CaO, Al2O3, B2O3, SiO2) using a flow-through system. The experiments were designed to measure the dissolution rate constant over the interval pH 1 through pH 13 at 3 temperatures (25°, 50° and 70°C). Dilute buffers were used to maintain a constant pH. Analyses of solutions and solid surfaces provided information that is used to develop a kinetic model for glass dissolution.Under all conditions we eventually observed linear dissolution kinetics. In strongly acidic solutions (pH 1 to pH 3) all components but Si were released in their stoichiometric proportions and a thick, Si-rich gel was formed. In mildly acidic to neutral solutions the gel was thinner and was both Si- and Al-rich, while the other components were released to solution in stoichiometric proportions. In mildly to strongly alkaline solutions all components were released to solution in stoichiometric proportions. By varying the flow rate at each pH we demonstrated a lack of transport control of the dissolution rate.The dissolution rates were found to be lowest at near-neutral pH and to increase at both low and high pH. A rate equation based on transition-state theory (TST) was used to calculate dissolution rate constants and reaction order with respect to pH over two pH intervals at each temperature. At 250C between pH 1 and pH 7 based on the Si release rate the log rate constant for glass dissolution (g glass/m20d) was −0.77 and the order with respect to pH was −0.48. Between pH 7 and pH 13 the log rate constant for glass dissolution was −8.1 and the order with respect to pH was +0.51. The measured simple glass dissolution rate constants compare very well with constants estimated by fitting the same TST equation to experimental results obtained for SRL-165 glass and to dissolution rate estimates made for synthetic basaltic glasses.


2016 ◽  
Vol 720 ◽  
pp. 157-161
Author(s):  
Kohei Nagata ◽  
Toshiisa Konishi ◽  
Michiyo Honda ◽  
Mamoru Aizawa

A novel chelate-setting β-tricalcium phosphate (β-TCP) cement with anti-washout properties have been fabricated previously. This cement has been set on the basis of chelating ability of inositol phosphate (IP6). In this study, the ball-milling and surface-modification conditions of starting β-TCP cement powders were optimized in terms of bioresorbability. Starting powders were prepared by simultaneously ball-milling at 300 rpm for 3 h with 1 mm diameter ZrO2 beads and surface-modifying with 40 cm3 of 3000 ppm IP6 solution. The resulting starting powder was consisted of β-TCP single phase, and had high specific surface area of 48.3 m2∙g-1. Cement pastes were prepared by mixing the starting powder and the aqueous solution composed of 2.5 mass% sodium hydrogen phosphate, 1.5 mass% citric acid and 1.0 mass% sodium alginate at a powder/liquid ratio of 1/0.90 [g∙cm-3] for 2 min. After setting in pure water for 72 h, compressive strength of the cement specimens was higher than that of human cancellous bone. Dissolution rate of Ca2+ ions was measured by according to Japanese Industrial Standard T 0330-3. The results of Ca2+ ions dissolution rate test demonstrated that the cement specimens derived from the above starting powder were the highest dissolution rate among examined ones. This cement would be expected as bone fillers with high bioresobability.


1989 ◽  
Vol 176 ◽  
Author(s):  
William L. Bourcier ◽  
Dennis W. Peiffer ◽  
Kevin G. Knauss ◽  
Kevin D. McKeegan ◽  
David K. Smith

ABSTRACTA kinetic model for the dissolution of borosilicate glass, incorporated into the EQ3/6 geochemical modeling code, is used to predict the dissolution rate of a nuclear waste glass. In the model, the glass dissolution rate is controlled by the rate of dissolution of an alkalidepleted amorphous surface (gel) layer. Assuming that the gel layer dissolution affinity controls glass dissolution rates is similar to the silica saturation concept of Grambow [1] except that our model predicts that all components concentrated in the surface layer, not just silica, affect glass dissolution rates. The good agreement between predicted and observed elemental dissolution rates suggests that the dissolution rate of the gel layer limits the overall rate of glass dissolution. The model predicts that the long-term rate of glass dissolution will depend mainly on ion concentrations in solution, and therefore on the secondary phases which precipitate and control ion concentrations.


1996 ◽  
Vol 465 ◽  
Author(s):  
W. L. Ebert ◽  
S.-W. Tam

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.


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