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Design and Synthesis of Chemical Precursors to Boron Carbide

Published online by Cambridge University Press:  25 February 2011

Xiaoguang Yang
Affiliation:
Department of Chemistry and Biochemistry, University of California at Los Angeles, 405 Hilgard Ave., Los Angeles, CA 90024.
Stephen Johnson
Affiliation:
Department of Chemistry and Biochemistry, University of California at Los Angeles, 405 Hilgard Ave., Los Angeles, CA 90024.
Hadcing Zheng
Affiliation:
Department of Materials Science and Engineering, University of California at Los Angeles, 405 Hilgard Ave., Los Angeles, CA 90024.
Kevin Thorne
Affiliation:
Department of Materials Science and Engineering, University of California at Los Angeles, 405 Hilgard Ave., Los Angeles, CA 90024.
J. D. Mackenzie
Affiliation:
Department of Materials Science and Engineering, University of California at Los Angeles, 405 Hilgard Ave., Los Angeles, CA 90024.
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Abstract

The design of molecular and preceramic polymer precursors to boron carbide based ceramics is described. The goal was to design nonvolatile, tractable precursors to boron carbide with high ceramic yields. Molecular precursors containing carburane cages and acetylenie groups were synthesized and converted to nonvolatile, soluble preceramic polymers. Pyrolysis of these polymers gave boron carbide based ceramics in 60–70% ceramic yield. A B4C/SiC film has been fabricated from one of the polymers and the film is uniform and crack-free.

Type
Research Article
Copyright
Copyright © Materials Research Society 1992

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References

REFERENCES

[1] Wynne, K. J. and Rice, R. W., Ann. Rev. Mater. Sci 14, 297 (1984).Google Scholar
[2] Toreki, W., Polymer Newsie, 6 (1991)Google Scholar
[3] (a) Rice, R. W., Wynne, K. J., Fox, W. B., U. S. Patent No. 4,097,294 (1978).Google Scholar
(b) Walker, B.E Jr, Rice, R. W., Becher, P. E., Bender, B. A., Coblenz, W. S., Am. Ceram. Soc. Bull. 62, 916 (1983).Google Scholar
[4] Mirabelli, M. G. L. and Sneddon, L. G., J. Am. Chem. Soc. 110, 3305 (1988).Google Scholar
[5] Zheng, H., Thome, K., Mackenzie, J. D., Yang, X., Hawthorne, M. F., presented at the 1991 MRS Fall Meeting, Boston, MA.Google Scholar
[6] Wynne, K. J., in Transformation of Organometallics into Common and Exotic Materials: Design and Activation, edited by Laine, R. M., Matrinus Nijhoff Publisher, 1988, p 8996.Google Scholar
[7] Reactive Oligomers, edited by Harris, F. W. and Spinelli, H. J. (ACS Symposium Series 282, St. Louis, MO, 1984) pp 1729.Google Scholar
[8] Zakharkin, L. I., Kovderov, A. I., Ol'Shevskaya, V. A., Izv. Akad. Nauk SSSR, Ser. Khim. 25, 1388 (1986).Google Scholar
[9] Yang, X., Knobler, C. B., Hawthorne, M. F., unpublished results.Google Scholar
[10] Grimes, R., Carboranes, Academic Press, New York 1970, p181.Google Scholar
[11] Miller, J. A. and Zweifel, G., Synthesis 129 (1983).Google Scholar