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Experimental Indications of Effects of Surface Deprotonation on Na-Bentonite Porewater Chemistry in a Geological Repository

Published online by Cambridge University Press:  21 March 2011

C. Oda
Affiliation:
Japan Nuclear Cycle Development Institute, Tokai, Ibaraki, Japan. Email: chie@tokai.jnc.go.jp
M. Shibata
Affiliation:
Japan Nuclear Cycle Development Institute, Tokai, Ibaraki, Japan. Email: chie@tokai.jnc.go.jp
M. Yui
Affiliation:
Japan Nuclear Cycle Development Institute, Tokai, Ibaraki, Japan. Email: chie@tokai.jnc.go.jp
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Abstract

Bentonite-water interaction was studied using a simple equilibrium model based on experimental measurements in order to describe bentonite porewater chemistry. Direct pH measurements for highly compacted bentonite and batch-type bentonite-water interaction experiments were performed under anaerobic conditions. In the direct pH measurements, resin particles doped with a pH indicator were sandwiched between a pair of bentonite columns immersed in a test solution. The experimental results showed that the solution compositions in equilibrium with bentonite depended on the bentonite to liquid ratio (B/L) and the initial solution composition. An equilibrium model assuming only fast equilibration processes between the bentonite minerals and the solution could be used to calculate the trends of pH and other ion concentrations with B/L. This study indicates that the surface deprotonation of smectite is a very important factor influencing the porewater chemistry in highly compacted bentonite.

Type
Research Article
Copyright
Copyright © Materials Research Society 2001

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References

REFERENCES

1. Wanner, H., EIR-Bericht Nr. 589 (1986).Google Scholar
2. Wieland, E., Wanner, H., Albisson, Y., Wersin, P. and Karnland, O., SKB Technical Report 94-26 (1994).Google Scholar
3. Bradbury, M. H. and Baeyens, B, PSI Bericht Nr. 95-12 (1995).Google Scholar
4. Owada, H., Mihara, M., Iriya, K. and Matsui, A., JNC TN8400 99-057 (in Japanese) (1999).Google Scholar
5. Sasaki, Y., Shibata, M., Yui, M. and Ishikawa, H., Scientific Basis for Nuclear Waste Management XVIII, Mat. Res. Soc. Symp. Proc., vol.353, pp.337344 (1994).Google Scholar
6. Gaines, G. L. and Thomas, H. C., J. Chem. Phys, 21, pp.714718 (1953).Google Scholar
7. Dzombak, D. A. and Morel, F. M. M., Surface Complexation Modeling, A Wiley-Interscience Publication (1990).Google Scholar
8. Shibutani, T., Kohara, Y., Oda, C., Kubota, M., Kuno, Y. and Shibata, M., JNC TN8400 99-066 (in Japanese) (1999).Google Scholar
9. Parkhurst, D. L., U.S. Geological Survey, Water-Resources Investigations Report 95-4227 (1995).Google Scholar
10. Yui, M., Takeda, S., Komuro, M., Makino, H., Shibutani, T., Umeki, H., Ishiguro, K., Takase, H. and Neyama, A., PNC TN8410 92-166 (in Japanese) (1992).Google Scholar