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Electrochemical Synthesis of Zirconia

Published online by Cambridge University Press:  25 February 2011

Jay A. Switzer  and
Richard J. Phillips
Jay A. Switzer
Affiliation:
University of Pittsburgh, Department of Materials Science and Engineering, 848 Benedum Hall, Pittsburgh, PA 15261
Richard J. Phillips
Affiliation:
University of Pittsburgh, Department of Materials Science and Engineering, 848 Benedum Hall, Pittsburgh, PA 15261
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Abstract

Zirconia powder was produced in aqueous solution from zirconyl nitrate using electrogenerated base. Both divided and undivided electrochemical cells were used. In the divided cell, hydroxide ion was discharged in the cathode compartment, and hydrated zirconia was produced. The as-produced material was weakly agglomerated, amorphous, and had a surface area of up to 316 m2/g. The surface area of the powder did not vary systematically with the electrosynthesis current density, but did depend on subsequent processing. Crystalline zirconia was produced by calcining in air at temperatures above 400°C. Tetragonal zirconia was the only phase observed until about 800°C. After calcining at 800°C the crystallite size increased to about 20nm and about 34% monoclinic zirconia was produced. When an undivided cell was used, the pH remained constant (1–1.5) throughout the electrosynthesis, and amorphous zirconia deposited on the cathode.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 121: Symposium H – Better Ceramics Through Chemistry III , 1988 , 111
Copyright
Copyright © Materials Research Society 1988

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References

REFERENCES

Switzer, J.A., Am. Ceram. Soc Bull., 66, 1521 (1987).Google Scholar
2. Switzer, J.A., J. Electrochem. Soc, 133, 722 (1986).CrossRefGoogle Scholar
3. Garvie, R.C., J. Phys. Chem., 69, 1238 (1965).Google Scholar
4. Mazdiyasni, K.S., Lynch, C.T., and Smith, J.S., J. Am. Ceram. Soc, 48, 372 (1964).CrossRefGoogle Scholar
5. Mitsuhashi, T., Ichihara, M., and Tatsuke, U., J. Am. Ceram. Soc, 57, 97 (1974).CrossRefGoogle Scholar
6. Garvie, R.C. and Goss, M.F., J. Mater. Sci., 21, 1253 (1986).CrossRefGoogle Scholar
7. Morgan, P.E.D., J. Am. Ceram. Soc, 67, C–204 (1984).CrossRefGoogle Scholar
8. Toraya, H., Yoshimura, M., and Somiya, S., J. Am. Ceram. Soc, 67, C–119 (1984).CrossRefGoogle Scholar