The Growth and the Reaction Mechanism of Si3N4 Powder from Silica

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The behaviour of silica during the carbothermal reduction nitriding process at temperatures between 1300-1500°C was studied by means of X-ray diffraction and scanning electron microscope analysis. The experimental runs were allowed to proceed up to 1 h in presence of nitrogen flow. The following mechanism of reduction nitriding of silica which was based on the experimental observation was proposed. Initially the impurity of the starting material is reduced before 1300°C. SiO2 was reduced into SiO gas phase by active carbon and it was vaporised out of the mixture. The nucleation of α-Si3N4 was formed vapour-gas reaction took place and deposited on the surface of the mixture as well as around the reaction crucible. In the third stage, α-Si3N4 transforms to one dimensional direction which was β-Si3N4 particle. This was followed by the formation of SiC at temperature above 1450°C.

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157-162

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August 2007

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© 2007 Trans Tech Publications Ltd. All Rights Reserved

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[1] A. Gugel, et al. Powder Met. Int. Vol. 6 10 (1994), p.136.

Google Scholar

[2] C. Bowen, et al: J. Mat. Sci. Vol. 13 (1978), p.341.

Google Scholar

[3] I. Chen and A. Rosenflanz: Nature Vol. 389 16 (1997), p.701.

Google Scholar

[4] G. Z. Cao and R. Metselaar: Chem Mat. Vol. 3 2 (1991), p.242.

Google Scholar

[5] W. D. Glaeser: Ceramics for High Temperature Appl. -II (B. Hill Publications, Mass 1978).

Google Scholar

[5] W. R Cannon, et al.: J. Am. Ceram. Soc. Vol. 65 (1982), p.324.

Google Scholar

[6] M. Ekelund, et al: J. Mat. Sci. Vol. 31 (1996), p.5749.

Google Scholar

[7] T. Yamada: Am. Ceram. Soc. Bull. Vol. 72 5 (1993), p.99.

Google Scholar

[8] Z. G. Kostic, et al.: Ceramic Inter. Vol. 22 (1996), p.179.

Google Scholar

[9] R Reidel and W. Dressler: Ceramic Inter. Vol. 22 (1996), p.233.

Google Scholar

[10] M . Mori, US Patent no 4122152, (1977).

Google Scholar

[11] K. Komeya and H. Inoue: J. Mat. Sci. Vol. 10 (1975).

Google Scholar

[12] S. C. Zhang and W. R Canon: J. Am. Ceram. Soc. Vol. 67 10 (1984), p.691.

Google Scholar

[13] Y. W. Cho and Charles: J. A., Mat. Sci. and Tech. Vol. 7 (1991), p.399.

Google Scholar

[14] I. A Rahman: Ceramic Inter. Vol. 20 (1994), p.195.

Google Scholar

[15] A. Bannyapadhyay, et al: Scripta Met. Vol. 32 (1995), p.1417.

Google Scholar

[16] C. Bishop and Hendry: J. Thermal Analysis Vol. 42 (1994), p.697.

Google Scholar

[17] A. O. Kurt and J. T. Davies : J. Mat. Sci. Vol. 36 (2001), p.5885.

Google Scholar

[18] A. Atasoy and M. Tumer: 4 th Inter. Pow. Metall. Conf. Sakarya (2004), p.958.

Google Scholar

[19] B. K. Padhi and C. Potnaik: Cer. Inter. Vol 21 (1995), p.213.

Google Scholar

[20] H. Arik: Tr. J. Eng. and Enverimental Sci. Vol. 20 (1996), p.233.

Google Scholar

[21] Y. Sugahara, et al: J. Mat. Sci. Lett. Vol. 4 (1985), p.928.

Google Scholar

[22] A Atasoy and M. Tumer: 4 th Inter. Pow. Metall. Conf. Sakarya (2004), p.1299.

Google Scholar

[23] J. Krestan et al: J. Europ. Cer. Soc. Vol. 24 (2004), p.791.

Google Scholar

[24] E. T. Turkdogan: Metall. Trans Vol. 10 B (1977), p.308.

Google Scholar

[25] O. P. Kolchin: S. Africa, M. Mater. Symp. (1966), p.40.

Google Scholar

[26] I. Barin: Thermochemical Properties of Inorganic Materials, (S. Verlag Publications 1994).

Google Scholar