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Multiphase Electrodispersion Precipitation of Zirconia Powders

Published online by Cambridge University Press:  21 February 2011

Michael T. Harris
Affiliation:
Chemical Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831
Warren G. Sisson
Affiliation:
Chemical Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831
Timothy C. Scott
Affiliation:
Chemical Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831
Osman A. Basaran
Affiliation:
Chemical Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831
Charles H. Byers
Affiliation:
Chemical Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831
W. Ren
Affiliation:
Materials Science and Engineering Department, University of Tennessee, Knoxville, Tennessee 37996
Thomas T. Meek
Affiliation:
Materials Science and Engineering Department, University of Tennessee, Knoxville, Tennessee 37996
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Abstract

The multiphase electrodispersion precipitation of zirconia powders has been done in the electric dispersion reactor (EDR). This paper presents the first results obtained where the bench-scale EDR unit was operated in the continuous mode to synthesize 130 ± 2 g of ZrO2 powder in approximately 12 h. An aqueous solution of zirconyl nitrate was dispersed and precipitated in a 2-ethyl-l-hexanol continuous phase containing 0.012 M to 0.12 M ammonia. A gravity settler was used to remove soft agglomerates of the ZrO2 particles from the organic solvent. Electric bed filtration was employed to remove the fines from the solvent, which was then recycled.

The particle-size distribution was varied by changing the electric field strength. At high field strengths (approximately 20 kV/cm), the particle sizes ranged from approximately 0.1 to 5 μm. The dried powder had a consistency of talcum powder. Microwave and conventional heating experiments showed that the powders were sinterable. The BET surface area of the powders ranged from approximately 20 to 90 m2/g.

Type
Research Article
Copyright
Copyright © Materials Research Society 1998

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References

REFERENCES

1 Hardy, A.B., et al. , in Ultrastructure Processing of Advanced Ceramics, edited by Mackenzie, J. and Ulrich, D. R., John Wiley and Sons, New York, 1988) pp. 407428.Google Scholar
2 Osseo-Asare, K., and Arriagada, F.J., Ceram. Trans. 12, 3 (1990).Google Scholar
3 Harris, M.T., Scott, T.C., and Byers, C.H., U. S. Patent No. 5 122 360 (16 June 1992).Google Scholar
4 Harris, M.T., Scott, T.C., and Byers, C.H., U. S. Patent No. 5 207 973 (4 May 1993).Google Scholar
5 Harris, M.T., Scott, T.C., Basaran, O.A., and Byers, C.H., Mat. Res. Soc. Proc. 121, 257 (1988).Google Scholar
6 Harris, M.T., Sisson, W.G., and Basaran, O.A., Mat. Res. Soc. Proc. 271, 945 (1992).Google Scholar
7 Harris, M.T., Scott, T.C., and Byers, C.H., Mat. Sei. Eng. A168, 125 (1993).Google Scholar