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Dissolution Rate of Colloidal Silica in Highly Alkaline Solution

Published online by Cambridge University Press:  17 March 2011

Taiji Chida
Affiliation:
Department of Quantum Science and Energy Engineering, Graduate School of Engineering, Tohoku University, Sendai 980-8579, JAPAN
Yuichi Niibori
Affiliation:
Department of Quantum Science and Energy Engineering, Graduate School of Engineering, Tohoku University, Sendai 980-8579, JAPAN
Osamu Tochiyama
Affiliation:
Department of Quantum Science and Energy Engineering, Graduate School of Engineering, Tohoku University, Sendai 980-8579, JAPAN
Hitoshi Mimura
Affiliation:
Department of Quantum Science and Energy Engineering, Graduate School of Engineering, Tohoku University, Sendai 980-8579, JAPAN
Koichi Tanaka
Affiliation:
Department of Quantum Science and Energy Engineering, Graduate School of Engineering, Tohoku University, Sendai 980-8579, JAPAN
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Abstract

For the performance assessment of the radioactive waste repository, it is important to clarify the dynamic behavior of silica (silicic acid and hydrous or unhydrous silicon dioxides). The behavior of silica would be complicated when cement is used for the construction of the repository, since silica takes various forms due to polymerization, precipitation and dissolution with change of pH or temperature. In order to know the fundamental kinetic property of silica, this study has examined the dissolution rate of colloidal-silica.

In the experiment, the concentration of silica in a soluble form was determined by the silicomolybdenum-yellow method. In this study, soluble-silica was defined as silica reacting with molybdate reagent and coloring yellow, and colloidal-silica was defined as silica in liquid phase except for soluble-silica. Colloidal-silica was obtained through the polymerization process, where the pH value of silica solution was brought down from over 10 by HNO3 solution. This study examined dissolution rate of colloidal-silica again by setting to 10 or 13 in pH-value and 288 K, 298 K or 313 K in temperature. In the experimental results, the dissolution reaction of colloidal-silica proceeded linearly with time, when the dissolution of colloidal silica was not restricted by the solubility of silica. To estimate the dissolution rate, we assumed df /dt = k*, where f is the soluble-silica fraction defined as the amount of soluble-silica divided by the silica amount introduced into the sample solution, t the time (s) and k* the rate constant (s-1). The activation energy for the dissolution of the colloidal-silica at pH 13 was estimated to be approximately 80 kJ·mol-1which was similar to that for amorphous silica (solid phase) at pH 13. This suggests the same reaction mechanism for the dissolution of colloidal-silica and amorphous silica in highly alkaline solution.

Type
Research Article
Copyright
Copyright © Materials Research Society 2004

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References

1. Niibori, Y., Kunita, M., Tochiyama, O. and Chida, T., J. Nucl. Sci. Technol, 37, 349 (2000).Google Scholar
2. Chida, T., Niibori, Y., Tochiyama, O., Tanaka, K., in Science Basis for Nuclear Waste Mnagement XXVI, edited by Fintch, J. R. and Bullen, B. D., (Mater. Res. Soc. Proc., 757, Warrendale, PA, 2002) pp. 497502.Google Scholar
3. Howard, G. A., Aquqtic Environmental Chemistry, (Oxford Chemistry Primers, New York, 1996), p. 14.Google Scholar
4. Stumm, W., Morgan, J. J., Aquatic Chemistry, 3rd ed. (John Wiley & Sons, New York, 1996), p. 368.Google Scholar
5. Fleming, B. A., J. Colloid Interface Sci., 110, 40 (1986).Google Scholar
6. Carroll, S., Mroczek, E., Alai, M. and Ebert, M., Geochim. Cosmochim. Acta 62, 1379 (1998).Google Scholar
7. Hrnecek, E. and Irlweck, K., Radiochim. Acta. 87, 29 (1999).Google Scholar
8. Brady, V., , P., Walther, V., J., Geochim. Cosmochim. Acta 53, 2823 (1989).Google Scholar
9. Levenspiel, O., Chemical Reaction Engineering, 2nd ed. (John Wiley & Sons, New York, 1972), p. 834.Google Scholar
10. Atkins, W., , P., Physical Chemistry, 6th ed. (Oxford University Press, 1998), p. 775786.Google Scholar