Chemical Stability of Simiulated HLW Forms in Contact With Clay Media

1981 ◽  
Vol 11 ◽  
Author(s):  
P. Van Iseghem ◽  
W. Timmerans ◽  
R. De Batist

ABSTRACTThe corrosion stability of six simulated HLW forms proposed by several European countries (five borosilicate glasses and one borosilicate glass ceramic) in contact with different media relating to the clay disposal has been investigated for periods up to 80 days and at a surface area to solution volume ratio of 1 cm−1 under non de-aerated conditions. In the reference medium distilled water the corrosion stabilities are largely determined by saturation effects for elements such as Si, Ca, Mg, Sr, Fe and U. Si saturation is found to be enhanced by a large Al2O3 concentration in the glass. In the clay-water mixture these saturation effects are much less predominant. Wet clay attacks the waste forms faster than the clay-water mixture, although the corrosion rates tend to decrease with time in both clay media. In general, no simple Arrhenius-type temnnerature dependence for the corrosion behaviour is found for the interval between 40 and 200°C.

1983 ◽  
Vol 26 ◽  
Author(s):  
J. L. Woolfrey ◽  
D. M. Levins

ABSTRACTThe chemical durability of SYNROC C has been measured as a function of repository conditions, namely, temperature, surface/volume ratio, groundwater pH and composition. The leach rate of SYNROC C is less dependent on temperature than borosilicate glasses; activation energies range from 15-25 kJ mol-1 compared to 33-74 kJ mol-1 for glass. The rate of release from SYNROC C is very low and independent of solution composition for the solutions studied. There is little variation in leach rate over the pH range 4-9, but at pH 2 the rate is up to 10 times higher. SYNROC C leach rate is independent of flow rate or surface/volume ratio for the mobile waste elements because of the unimportance of solution saturation effects owing to the low concentration of dissolved solids. The differential leach rate decreases rapidly with time because, after initial leaching from grain boundaries and metastable minor phases, the highly insoluble matrix protects the more leachable elements from further attack.


2018 ◽  
Vol 1 (1) ◽  
pp. 12-18
Author(s):  
Enikő Bitay ◽  
Irén Kacsó ◽  
Erzsébet Veress

Abstract ZrO2 doped Na-Ba-borosilicate glasses suitable as matrix materials for HLW immobilization were synthesized and corrosion behaviour was investigated in different aqueous media. Hydrolytic stability is increased with the doping level until 5 mol %; above this value the glass vitrification tendency is strongly intensified. Unexpectedly, ZrO2 doping diminished the corrosion stability in 1M HCl solution, and low ZrO2 content showed a low corrosion resistance in 1M Na2CO3 solution also. Doping effect was negligible in case of synthetic seawater. The glass structure is significantly stabilized by the integration of the 30% UO3 added.


1988 ◽  
Vol 127 ◽  
Author(s):  
H. Roggendorf ◽  
R. Conradt ◽  
H. Schmidt

ABSTRACTBorosilicate glasses are proposed as waste form for the final disposal of High Level Waste (HLW) in salt formations by the Federal Republic of Germany. To check the safety of this waste form the corrosion of the non-radioactive borosilicate glass R7T7 in salt brines has been studied in collaboration with the Hahn-Meitner-Institut, Berlin. Temperatures up to 190°C and S/V ratios (surface area to solution volume ratio) between 3.3 and 1000 m were applied. S/V was varied by the addition of glass powder. The results presented here concern the characterization of the surface composition of the corroded glass (corroded at 190°C in a brine containing high amounts of MgCl-, called Q brine in this paper) after removing the reaction product layer. The corrosion conditions were chosen to obtain samples typical of long term (silica saturation) corrosion. The surface composition was analyzed quantitatively by X-ray photoelectron spectroscopy (XPS) by using external standard glasses with a composition similar to R7T7. Additionally scanning electron microscopy (SEM) was employed.


2015 ◽  
Vol 1744 ◽  
pp. 153-161 ◽  
Author(s):  
Michael I. Ojovan ◽  
William E. Lee

ABSTRACTThe pH-dependence of glass corrosion rates has a well-known U-shaped form with minima for near-neutral solutions. This paper analyses the change of U-shaped form with time and reveals that the pH dependence evolves even for solutions that have pH not affected by glass corrosion mathematically corresponding to a zero surface to volume ratio. The U(t) dependence is due to changes of concentration profiles of elements in the near-surface layers of glasses in contact with water and is most evident within the initial stages of glass corrosion at relatively low temperatures. Numerical examples are given for the nuclear waste borosilicate glass K-26 which is experimentally characterised by an effective diffusion coefficient of caesium DCs = 4.5 10-12 cm2/day and by a rate of glass hydrolysis in non-saturated groundwater as high as rh = 100 nm/year The changes of U-shaped form need to be accounted when assessing the performance of glasses in contact with water solutions.


1987 ◽  
Vol 109 (3) ◽  
pp. 325-330 ◽  
Author(s):  
C. L. Spiro ◽  
S. G. Kimura ◽  
C. C. Chen

Chemical and physical transformations of coal ash during combustion and deposition in gas turbine environments have been studied. Extensive characterization of the coal-water mixture fuel and deposits obtained on deposition pins and turbine nozzle vanes has been performed. The behavior of alkali metals has been found to be much different from that for petroleum fuels, resulting in lower than expected deposition and probable reduced corrosion rates.


2007 ◽  
Vol 336-338 ◽  
pp. 1780-1783 ◽  
Author(s):  
N. Maier ◽  
K.G. Nickel ◽  
Georg Rixecker

Corrosion experiments on a number of rare earth di-silicates containing Y, Yb and Lu have been conducted in flowing air with 30 vol.% H2O at 1500°C. Nominally the corrosion rate is slower by a factor 5 to 10 compared to silica. However, alumina impurity incorporation has a profound influence on the process of corrosion as it masks not only the gravimetric results but also changes the surface phase assemblages to contain rare earth garnets and liquid phases. It is presumed that silica loss occurs under those conditions via the liquid phase and does not necessarily follow the same kinetics as direct silicate corrosion. Furthermore, atmospheric silicon hydroxide saturation effects contribute to the corrosion process. Currently all determined corrosion rates of rare earth silicates are viewed as system specific only.


1993 ◽  
Vol 333 ◽  
Author(s):  
A. Loida ◽  
B. Grambow ◽  
P. Dressier ◽  
K. Friese ◽  
H. Geckeis ◽  
...  

ABSTRACTHigh-burnup (<50 MWd/kgU) spent fuel samples of various sizes were exposed to NaCl solutions under static, anaerobic and reducing conditions. The accumulated corrosion time was about 200 days. Gas phase and leach solutions were analyzed. By dissolving mm sized fragments in large volumes of solution, saturation effects were avoided and upper limits for intrinsic dissolution rates of about 5-20 mg/(m2d) were measured. Surface area normalized reaction rates were significantly lower when using fine grained fuel powder (estimated sample surface area to solution volume ratio S/V ca. 3000 m-1), indicating saturation effects. The maximum concentrations of Pu and Am in the tests are close to reported solubility limited concentrations in pure 5m NaCl solutions in the absence of radiolysis effects. The presence of iron effectively reduces the solution concentration of all measured radionuclides (except Cs).


Author(s):  
Michael I. Ojovan ◽  
Natalia V. Ojóvan ◽  
Irene V. Startceva ◽  
Zoja I. Golubeva ◽  
Alexander S. Barinov

Abstract A mathematical model was used to predict radionuclide release from bitumen and glass waste forms over extended time periods. To calculate some model parameters, we used experimental data derived from 12yr field tests with six borosilicate waste glass blocks (each ∼30 kg in weight) and a bitumen block (310 kg), containing real intermediate-level NPP operational waste (NaNO3, 86 wt.% of a dry salt content; 137Cs, 82% of the radioactive inventory). Specific radioactivities of the glass material containing 35 wt.% waste oxides were βtot(90Sr+90Y), 3.74×106 Bq/kg, and αtot(239Pu), 1.3×104Bq/kg. The bitumen block with ∼31 wt.% salt content and βtot(90Sr+90Y), 4.0·106 Bq/kg, and αtot(239Pu), 3.0×103 Bq/kg was manufactured on base of a hard bitumen BN-IV. Tests with the waste forms were performed under saturated conditions of an experimental near-surface repository with a free access of groundwater to the waste blocks through a covering of host loamy soil and backfill of coarse sand. The way used to quantify the amount of leached radioactivity was to measure the volume and radioactivity concentrations of contacting groundwater. In the model, radionuclide release from the waste glass is assumed to be controlled by the processes of diffusion limited ion exchange and glass network dissolution. The mechanism of radionuclide release from the bitumen matrix is believed to remain the same throughout the long-term storage period, except for the initial stage when an enhanced leaching from the surface layer occurs. This long-term release is assumed to be controlled by diffusion of radionuclides through the bitumen matrix. So, identical formulae were applied to calculate the values of leached radioactivity fractions for two waste forms. Radioactivity release curves were plotted for field data and calculation results. For both waste forms, there was good agreement between the modelled and available experimental data. According to the modelling results, fmax = 2.3×10−3% of the initial radioactivity will release from the waste glass into the environment within a proposed institutional control period of 300 years under conditions of the near-surface repository and in the absence of additional engineered barriers. For the bitumen block and the same 300-yr period, the total (maximum) leached radioactivity fraction will be fmax = 4.2×10−3%. The main result of the modelling and experimental studies concerning the leaching behaviour of the bituminised and vitrified waste materials is that the fractional radioactivity release for two waste forms is on the same order of magnitude. Numerical release values per a unit of a surface area to volume ratio are also rather close for two waste forms (exposed surface area to volume ratio for the bitumen block is 2 to 4 times greater then for the glass).


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

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