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Weight loss and gas evolution during sintering of silicon nitride powders synthesized by silica reduction and imide decomposition

Published online by Cambridge University Press:  31 January 2011

Yasuhiro Goto
Affiliation:
Materials and Devices Research Laboratories, Research and Development Center, Toshiba Corporation, 1, Komukai Toshiba-cho, Saiwai-ku, Kawasaki 210, Japan
Yoshiyuki Ohnuma
Affiliation:
Materials and Devices Research Laboratories, Research and Development Center, Toshiba Corporation, 1, Komukai Toshiba-cho, Saiwai-ku, Kawasaki 210, Japan
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Extract

The relationships among weight loss, gas evolution, and other changes during sintering were investigated for silicon nitride powders synthesized by silica reduction and imide decomposition. Small weight losses were detected for all powders at low temperatures (below 1400 °C), and large weight losses were found to occur for the silica-reduction powders at high temperatures (1400–1800 °C). Only CO was detected in the sampled gases during sintering, and CO evolution peaks were seen at around 900–1200 (broad), 1400, and 1600 °C. The main deposited material around the samples was SiO. The weight losses at low temperatures were thought to be caused by evaporation of residual binder or adsorbed substances. The main causes of the large weight losses at high temperatures were thought to be CO and SiO evolutions, and CO evolution at around 1600 °C probably originated from the liquid phase accompanied by α–Si3N4 to β–Si3N4 transformation.

Type
Articles
Copyright
Copyright © Materials Research Society 1998

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References

1.Glasson, D. R. and Jayaweera, S. A. A., J. Appl. Chem. 18, 65 (1968).CrossRefGoogle Scholar
2.Zhang, S-C. and Cannon, W. R., J. Am. Ceram. Soc. 67, 691 (1984).CrossRefGoogle Scholar
3.Komeya, K. and Inoue, H., J. Mater. Sci. 10, 1243 (1975).CrossRefGoogle Scholar
4.Inoue, H., Komeya, K., and Tsuge, A., J. Am. Ceram. Soc. 65, C-205 (1982).Google Scholar
5.Mazdiyasni, K. S. and Cooke, L. M., J. Am. Ceram. Soc. 56, 628 (1973).Google Scholar
6.Yamada, T., Kawahito, T., and Iwai, T., in Proc. Int. Sympo. Ceram. Comp. Engines, edited by Sōmiya, S., Kanai, E., and Ando, K. (Elsevier Appl. Sci., London, 1983), p. 333.Google Scholar
7.Yamada, T. and Kohtoku, Y., Jpn. Chem. Ind. Assn. Monthly 42, 8 (1989).Google Scholar
8.Richerson, D. W., Am. Ceram. Soc. Bull. 52, 560 (1973).Google Scholar
9.Lnage, F. F., J. Am. Ceram. Soc. 62, 428 (1979).Google Scholar
10.Kohtoku, Y., FC Report 11, 257 (1993).Google Scholar
11.Yamada, T., Kanetsuki, Y., Fueda, K., Takahashi, T., Kohtoku, Y., and Asada, H., in Key Engineering Materials, Vols. 89–91, “Silicon Nitride ‘93,” edited by Hoffmann, M. J., Becher, P. F., and Petzow, G. (Trans Tech Publications, Switzerland, 1994), p. 177.Google Scholar
12.Dijen, F. K., Kerber, A., Vogt, U., Pfeiffer, W., and Schulze, M., in Key Engineering Materials, Vols. 89–91, “Silicon Nitride ‘93,” edited by Hoffmann, M. J., Becher, P. F., and Petzow, G. (Trans Tech Publications, Switzerland, 1994), p. 19.Google Scholar
13.Komeya, K., Funahashi, K., Meguro, T., and Kameda, T., in Advanced Materials ‘93, I/A: Ceramic Powders, Corrosion and Advanced Processing, edited by N. Mizutani, Trans. Mat. Res. Soc. Jpn. 14A, 915 (1993).Google Scholar
14.Suzuki, K. and Kanno, Y., J. Ceram. Soc. Jpn. 92, 101 (1984).Google Scholar
15.Inoue, H., Komeya, K., and Tsuge, A., Toshiba Rev. 39, 488 (1984).Google Scholar