Hostname: page-component-848d4c4894-wzw2p Total loading time: 0 Render date: 2024-05-17T19:17:08.991Z Has data issue: false hasContentIssue false

Processing of Nanostructured Zirconia Ceramics

Published online by Cambridge University Press:  15 February 2011

G. Skandan
Affiliation:
Dept. of Materials Science and Engineering, Rutgers, The State University of New Jersey, P.O. Box 909, Piscataway, NJ 08855, U. S. A.
H. Hahn
Affiliation:
Technische Hochschule Darmstadt 31 Hilperstr., Darmstadt, Germany
B. H. Kear
Affiliation:
Dept. of Materials Science and Engineering, Rutgers, The State University of New Jersey, P.O. Box 909, Piscataway, NJ 08855, U. S. A.
M. Roddy
Affiliation:
Dept. of Ceramic Engineering, Rutgers, The State University of New Jersey, P.O. Box 909, Piscataway, NJ 08855, U. S. A.
W. R. Cannon
Affiliation:
Dept. of Ceramic Engineering, Rutgers, The State University of New Jersey, P.O. Box 909, Piscataway, NJ 08855, U. S. A.
Get access

Abstract

The inert gas condensation (IGC) technique was employed to synthesize non-agglomerated nanoparticles of ZrO2 and Y2O3 with different average particle sizes ranging from 4 to 14 run. The sintering behaviors (in air and vacuum) of single phase n-ZrO2 (monoclinic crystal structure) and Y2O3-ZrO2 mixture (Y-TZP) were studied in terms of densification rate and final sintering temperature. There was a strong correlation between densification characteristics and properties of the starting powder compacts such as average particle size, particle and pore size distributions. n-ZrO2 was sintered to full density in air at temperatures as low as 1125°C (0.47 Tm) and in vacuum at 975 °C (0.42 Tm). Although the grain sizes in the fully sintered samples were well below 100 nm, the grains had grown by a factor of 10 as compared to the initial particle size. Therefore, a pressureassisted sintering technique was employed to further reduce the densification temperature and final grain size. Threshold effects in this process are also discussed.

Type
Research Article
Copyright
Copyright © Materials Research Society 1994

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. Gleiter, H., Progress in Mat. Sci., 33 (4) (1990).Google Scholar
2. Uyeda, R., Progress in Mat. Sci., 15 (5) (1991).Google Scholar
3. Siegel, R. W., Nanostructured Materials, 3, 1 (1993).Google Scholar
4. Kislyi, P. S., Kryl, Ya. A., Filipenko, V. M., Sverkhtverdye Materialy, 6, 2934 (1987).Google Scholar
5. Hahn, H. and Averback, R. S., Nanostructured Materials, 1, 95 (1992).Google Scholar
6. Messing, G., Zhang, S. and Jayanthi, G., J. Am. Ceram. Soc., 76 [11], 2707 (1993).Google Scholar
7. Cannon, W. R. and Danforth, S. C., J. of Am. Ceram. Soc., 65 [7], 324 (1982).Google Scholar
8. Birringer, R., Gleiter, H., Klein, H. P. and Marquardt, P., Phy. Lett. 102A, 365 (1984).Google Scholar
9. Skandan, G., Hahn, H. and Parker, J. C., Scripta Met., 25, 2389 (1991).Google Scholar
10. Skandan, G., Hahn, H., Roddy, M. and Cannon, W. R., J. Am. Ceram. Soc., in press.Google Scholar
11. Skandan, G., Foster, C. M., Frase, H., Ali, M. N., Parker, J. C. and Hahn, H., Nanostructured Materials, 1, 313 (1992).Google Scholar
12. Allen, A., Krueger, S., Long, G., Kerch, H., Parker, J. C., Skandan, G. and Hahn, H., to be published in the proceedings of World Ceramic Congress at Florence, Italy.Google Scholar
13. Skandan, G., Hahn, H., Kear, B. H., Roddy, M. and Cannon, W. R., to be published in Mat. Letters.Google Scholar
14. Swinkels, F. B. and Ashby, M. F., Acta Metail., 29 [2] 259 (1981).Google Scholar
15. Coble, R. L., J. of App. Phy., 41 (12), 4798 (1970).Google Scholar