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Synthesis of ceramic oxide powders in a microwave plasma device

Published online by Cambridge University Press:  03 March 2011

Dieter Vollath
Affiliation:
Kernforschungszentrum Karlsruhe, Institut für Materialforschung, P.O. Box 3640, D-76021 Karlsruhe, Germany
Kurt E. Sickafus
Affiliation:
Los Alamos National Laboratory, Los Alamos, New Mexico 87545
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Abstract

Synthesizing oxide ceramic powders by application of a microwave plasma is a great advantage. There are two ways the microwave plasma can be used: The first is as a source of heat for the pyrolysis of solutions and the second is to excite gas reactions to obtain nanosized powders. Both applications are superior to standard methods. A microwave cavity well suited for these experiments and its operating characteristics are described. Using a microwave plasma as a source of heat for pyrolytic decomposition of nitrates in aqueous solutions leads to a fine-grained product with particle sizes from 100 to 1000 nm. Crystallite sizes in those particles are in most cases less than 10 nm. This is demonstrated with zirconia-based ceramics, such as ZrO2−3 mol % Y2O3−20 mol % Al2O3. Depending on the conditions during pyrolysis, it is possible to obtain a product in which alumina is either dissolved in zirconia or the onset of the phase separation is observed. The energy efficiency of this process is better than 80%. If the reactants are gaseous, e.g., ZrCl4, it is possible to produce powders with mean particle sizes of about 4 nm. In the case of zirconia, these particles are monocrystalline with a cubic structure. This structure is not in equilibrium under the experimental conditions.

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Articles
Copyright
Copyright © Materials Research Society 1993

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References

REFERENCES

1Vollath, D., J. Mater. Sci. 25, 2227 (1990).CrossRefGoogle Scholar
2Vollath, D. and Dörzapf, B., Vorrichtung zur Herstellung von Keramikpulvern, German Patent G 90 15 477, May 3, 1992.Google Scholar
3Vollath, D., Euro-Ceiamics 1, 1.33 (1989).Google Scholar
4Vollath, D. and Dörzapf, B., Verfahren zur Herstellung homogener feinteiliger Keramikpulver, German Patent P 37 25 740.4, April 4, 1990.Google Scholar
5Vollath, D., Sickafus, K., and Varma, R., in Microwave Processing of Materials III, edited by Beatty, R.L., Sutton, W. H., and Iskander, M.F. (Mater. Res. Soc. Symp. Proc. 269, Pittsburgh, PA, 1992), p. 379.Google Scholar
6Vollath, D. and Sickafus, K. E., J. Mater. Sci. (1993, in press).Google Scholar
7Christiansen, D. Z. and Unruh, W. P., Ceram. Trans. 21, 597 (1991).Google Scholar
8Vogt, G. J. and Unruh, W. P., in Microwave Processing of Materials III, edited by Beatty, R.L., Sutton, W. H., and Iskander, M.F. (Mater. Res. Soc. Symp. Proc. 269, Pittsburgh, PA, 1992), p. 245.Google Scholar
9Singh, A. K., Mehta, P., and Kingon, A. I., Ceram. Trans. 21, 421 (1991).Google Scholar
10Vollath, D. and Sickafus, K. E., Nanostructured Mater. 1, 427437 (1992).CrossRefGoogle Scholar
11Gleiter, H., Prog, in Mater. Sci. 33, 223 (1989).Google Scholar
12Gleiter, H., Nanostructured Mater. 1, 1 (1992).CrossRefGoogle Scholar
13Kagawa, M., Honda, F., Onodera, H., and Nagae, T., Mater. Res. Bull. XVIII, 1081 (1983).Google Scholar
14Kagawa, M., Suzuki, M., Mizaguchi, Y., Hirai, T., and Syono, Y., MRS Spring Meeting '92, San Francisco, Abstract No. P2.3, (1992).Google Scholar
15Anderson, H., Kodas, T. T., and Smith, D. M., Am. Ceram. Soc. Bull. 68, 996 (1989).Google Scholar
16MacDonald, A. D., Microwave Breakdown in Gases (John Wiley & Sons, New York, 1966).Google Scholar
17Bosisio, R. G., Weissfloch, C. F., and Wertheimer, M. R., J. Microwave Power 7, 325 (1972).CrossRefGoogle Scholar
18Baker, R. R., Jacobs, A., and Winkler, C. A., Can. J. Chem. 49, 1671 (1971).CrossRefGoogle Scholar
19Young, R. A., Sharpless, R. L., and Stringham, R. J., J. Chem. Phys. 40, 117 (1964).CrossRefGoogle Scholar
20Schlick, G. GmbH, Coburg, Germany, Technical Document #D19/1.Google Scholar
21Phase Diagrams for Ceramists (The American Ceramics Society, Westerville, OH, 1981), pp. 141142.Google Scholar
22Gmelins Handbuch der anorganischen Chemie, Zirconium Syst. #42 (1958), p. 291.Google Scholar
23Phase Diagrams for Ceramists (The American Ceramics Society, Westerville, OH, 1975), pp. 7677.Google Scholar