Hostname: page-component-848d4c4894-2xdlg Total loading time: 0 Render date: 2024-06-20T06:28:19.643Z Has data issue: false hasContentIssue false

New Crystalline Silicotitanate (CST) Waste Forms: Hydrothermal Synthesis and Characterization of CS-SI-TI-O Phases

Published online by Cambridge University Press:  10 February 2011

M. Nyman
Affiliation:
Sandia National Labs, Org. 1845, M.S. 0710. Albuquerque, N.M. 87185-0710
T. M. Nenoff
Affiliation:
Sandia National Labs, Org. 1845, M.S. 0710. Albuquerque, N.M. 87185-0710
Y. Su
Affiliation:
Pacific Northwest Labs, P.O. Box 999, MSIN K8-93, Battelle Blvd., Richland, WA 99352
M. L. Balmer
Affiliation:
Pacific Northwest Labs, P.O. Box 999, MSIN K8-93, Battelle Blvd., Richland, WA 99352
A. Navrotsky
Affiliation:
U.C. Davis, Dept. of Chem. Eng. and Mat. Sci. U.C. Davis, Davis, CA 95616
H. Xu
Affiliation:
U.C. Davis, Dept. of Chem. Eng. and Mat. Sci. U.C. Davis, Davis, CA 95616
Get access

Abstract

The radioactivity of the Hanford site waste tanks is primarily from 137Cs and 90Sr, of which can both be selectively removed from solution using a crystalline silicotitanate (CST) ion exchanger. We are currently seeking waste forms alternative to borosilicate glass for Cs-CSTs. In order to obtain a fundamental basis for the development of an alternative waste form, we are investigating synthesis and characterization of CST component phases, namely Cs-Si-Ti-O phases. Two novel Cs-Ti-Si-O phases (one porous, one condensed) have been hydrothermally synthesized, characterized and evaluated as waste form candidates based on chemical and thermal stability, leachability, and ion exchange capabilities.

Type
Research Article
Copyright
Copyright © Materials Research Society 1999

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

[1] Anthony, R. G., Phillip, C. V., Dosch, R. G., Waste Management 13 (1993) 503512.Google Scholar
[2] Anthony, R. G., Dosch, R. G., Gu, D., Philip, C. V., Industrial Engineering and Chemical Research 33 (1994) 2702–2705.Google Scholar
[3] Poojary, D. M., Cahill, R. A., Cleartield, A., Chemistsry of Materiials 6 (1994) 23642368.Google Scholar
[4] Balmer, M. L.,, Pacific Northwest Labs, Chicago August, 1998.Google Scholar
[5] Balmer, M. L., Huang, Q., Wong-Ng, W., Roth, R. S., Santoro, A., Journal of Solid State Chemistry 130 (1997) 97–102.Google Scholar
[6] Balmer, M. L., Su, Y., Grey, I. E., Santoro, A., Roth, R. S., Huang, Q., Hess, N., Bunker, B. C., Materials Rescarch Societv Svinposium Proceedinigs 455 (1997) 449455.Google Scholar
[7] McCready, D. E., Balmer, M. L., Keefer, K. D., Powder Diffraction 12 (1997) 4046.Google Scholar
[8] Behrens, E. A., Poojary, D. M., Clearfield, A., Clhcnmistirm of Mateiials 8 (1996) 12361244.Google Scholar
[9] Harrison, W. T. A., Gier, T. E., Stucky, G. D., Zeolitcs 15 (1995) 408–412.Google Scholar
[10] Labouriau, A., Higley, T. J., Earl, W. L., Journal of physical Chemistry 102 (1998) 2897–2904.Google Scholar
[11] Dirken, P. J., Smith, M. E., Whitfield, H. J., Journal of Physical Chemistry 99 (1995) 395–401.Google Scholar
[12] Bunker, B. C., Pacific Northwest Laboratory, Richland 1994.Google Scholar