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Coprecipitation of Ni With Calcite: An Experimental Study

Published online by Cambridge University Press:  10 February 2011

T. Carlsson
Affiliation:
VTT Chemical Technology, P.O.Box 1404, FIN-02044 VTT, Finland, [email protected]
H. Aalto
Affiliation:
VTT Chemical Technology, P.O.Box 1404, FIN-02044 VTT, Finland, [email protected]
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Abstract

At the Finnish candidate sites for a nuclear waste repository calcite (CaCO3) is a common fracture mineral, that may participate in coprecipitation processes. The objective of this work was to study the coprecipitation of the trace element Ni with CaCO3 under controlled conditions. The experiments were carried out at 30 °C in vessels closed to the atmosphere. Calcite-saturated 0.05 M NaCI solutions containing trace amounts of Ni2+ were contacted with calcite for periods of up to 42 days. The experimental data indicate that Ni coprecipitates with calcite as a result of recrystallization. The amounts of coprecipitated Ni and recrystallized calcite were determined using liquid scintillation counting and the isotopes 63Ni and 45Ca. The results are supported by a complementary SEM/EDS analysis of the solid phase.

Type
Research Article
Copyright
Copyright © Materials Research Society 1998

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References

REFERENCES

1 Pitkanen, P., Snellman, M., Leino-Forsman, H., Nuclear Waste Commission of Finnish Power Companies, Report YJT-94-14, (1994).Google Scholar
2 Grenthe, I., Radiochim. Acta, 52/53, p. 425 (1991).Google Scholar
3 Read, D., Chemval-2 Project Report on Stage 1: ECSC-EC-EAEC, Report EUR 15161 (1993).Google Scholar
4 Bruno, J., Grenthe, I., Munoz, M., Mat. Res. Soc. Symp. Proc. 50, Pittsburgh, PA, p. 717 (1985)Google Scholar
5 Savage, D., Mat. Res. Soc. Symp. Proc. 353, Pittsburgh, PA, 1159 (1995)Google Scholar
6 Kolthoff, I. and Sandell, E.B., Textbook of Quantitative Inorganic Analysis, Mac Millan, New York, 3rd ed., 1952.Google Scholar
7 Schwarzenbach, G., Complexometric Titrations, Interscience, New York, 1957.Google Scholar
8 Morse, J. W. and Bender, M. L., Chem. Geol., Vol. 82, p. 265 (1990)Google Scholar
9 Meece, D. E. and Benninger, L. K., Geochim. Cosmochim. Acta, Vol. 57, p. 1447 (1993)Google Scholar
10 Ollila, K., J. Nuci. Mater., Vol. 190, p. 70 (1992)Google Scholar
11 Brunauer, S., Emmett, P.H., Teller, E., J. Am. Chem. Soc. Vol. 60, p. 309 (1938)Google Scholar
12 Lawrence, T. J. Wolery Livermore National Laboratory, Report UCRL-MA- 110662 PT III.Google Scholar
13 Carlsson, T. and Aalto, H., TVO Work Report TURVA-95-07, 1995.Google Scholar
14 Carlsson, T. and Aalto, H., VTT Research Notes 1793, 1996.Google Scholar
15 Stumm, W., Chemistry of the Solid-Water Interface, Wiley-Interscience, New York, 1991.Google Scholar
16 Lorens, R. B., Geochim. Cosmochim. Acta, Vol. 45, p. 533 (1981)Google Scholar
17 Smith, R. M. and Martell, A. E., Critical Stability Constants, Vol. 4. Plenum Press, London, 1976,Google Scholar
18 Grauer, R., Paul Scherrer Institut, TM-44-94-05, 1994.Google Scholar