Hostname: page-component-8448b6f56d-dnltx Total loading time: 0 Render date: 2024-04-25T06:19:07.827Z Has data issue: false hasContentIssue false
  • English
  • Français

Temperature effect on nonhydrolytic foaming process

Published online by Cambridge University Press:  31 January 2011

G. S. Grader ,
Y. de Hazan ,
G. Natali ,
T. Dadosh  and
G. E. Shter
G. S. Grader
Affiliation:
Chemical Engineering Department, Technion, Haifa 32000, Israel
Y. de Hazan
Affiliation:
Chemical Engineering Department, Technion, Haifa 32000, Israel
G. Natali
Affiliation:
Chemical Engineering Department, Technion, Haifa 32000, Israel
T. Dadosh
Affiliation:
Chemical Engineering Department, Technion, Haifa 32000, Israel
G. E. Shter
Affiliation:
Chemical Engineering Department, Technion, Haifa 32000, Israel
Get access

Abstract

This paper describes the effect of temperature on the formation of nonhydrolytic alumina foams. The foams are generated by heat treatment of crystals of the aluminum chloride isopropyl ether complex [AlCl3(Pri2O)], with the release of isopropyl chloride (PriCl). The chlorine content in the foams was determined by titration, and their weight loss during sintering was measured by thermogravimetric and differential thermal analysis. Based on these measurements, the condensation degree (CD) in the foams was modeled. The foaming time ranged from several minutes at 70 °C to several seconds at 160 °C. It was found that the chlorine-to-aluminum ratio of the foam (Cl/Al) decreased from 1.79 at 70 °C to 1.56 at 160 °C. Thermogravimetric analysis data confirm that the smaller Cl content gives rise to a smaller weight loss during thermal decomposition, consistent with a higher CD in the foams created at higher temperatures. Finally, about 80% of the PriCl produced during complex decomposition and subsequent –Al–O–Al– condensation reactions is lost during foaming.

Type
Articles
Information
Journal of Materials Research , Volume 14 , Issue 10 , October 1999 , pp. 4020 - 4024
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.Grader, G.S., Shter, G.E., and de Hazan, Y., Israeli Patent Application No. 123 969 (1998).Google Scholar
2.Grader, G.S., de Hazan, Y., and Shter, G.E., in Sol-Gel Processing, Proceedings of the American Ceramic Society Annual Meeting, edited by Komarneni, S. (American Ceramic Society, 1998).Google Scholar
3.Grader, G.S., de Hazan, Y., and Shter, G.E., J. Mater. Res. 14, 1485 (1999).CrossRefGoogle Scholar
4.Brockmeyer, J.W., U.S. Patent No. 4 610 832 (9 Sept 1986).Google Scholar
5.Lange, F.F. and Miller, K.T., Adv. Ceram. Mater. 2, 827 (1987).CrossRefGoogle Scholar
6.Fujiu, T., Messing, G.L., and Huebner, W., J. Am. Ceram. Soc. 73, 85 (1990).CrossRefGoogle Scholar
7.Wu, M. and Messing, G., J. Am. Ceram. Soc. 73, 3497 (1990).CrossRefGoogle Scholar
8.Sepulveda, P., Am. Ceram. Soc. Bull. 76, 61 (1997).Google Scholar
9.Even, W.R. Jr and Gregory, D.P., MRS Bull. XIX(4), 29 (1994).CrossRefGoogle Scholar
10.Grader, G.S., de Hazan, Y., Cohen, Y., and Bravozhivotovskii, D., J. Sol-Gel. Sci. Technol. 10, 5 (1997).CrossRefGoogle Scholar
11.Grader, G.S., de Hazan, Y., Bravo-Zhivotovski, D., and Shter, G.E., J. Sol-Gel Sci. Technol. 10, 127 (1997).CrossRefGoogle Scholar