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Synthesis behavior and grain morphology in mullite ceramics with precursor pH and sintering temperature

Published online by Cambridge University Press:  31 January 2011

Jae-Won Kim
Affiliation:
Department of Ceramic Science and Engineering, Changwon National University, Changwon, Kyungnam 641–773, Korea
Jae-Ean Lee
Affiliation:
Department of Ceramic Science and Engineering, Changwon National University, Changwon, Kyungnam 641–773, Korea
Yeon-Gil Jung*
Affiliation:
Department of Ceramic Science and Engineering, Changwon National University, Changwon, Kyungnam 641–773, Korea
Chang-Yong Jo
Affiliation:
High Temperature Materials Group, Korea Institute of Machinery and Materials, Changwon, Kyungnam 641–010, Korea
Jae-Ho Lee
Affiliation:
Department of Ceramic Engineering, Hanyang University, Seoul 133–791, Korea
Ungyu Paik
Affiliation:
Department of Ceramic Engineering, Hanyang University, Seoul 133–791, Korea
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Abstract

The effects of the precursor pH and sintering temperature on the synthesizing behavior and morphology of mullite were studied using a stoichiometric mullite (3Al2O3 · 2SiO2) precursor sol. The mullite precursor sol was prepared by the dissolution of aluminum nitrate enneahydrate [Al(NO3)3 · 9H2O] into the mixture of silica sol. The precursor pH of the sols was controlled to the acidic (pH ≈ 1.5 to 2), intermediate (pH ≈ 4.5 to 5) and basic (pH ≈ 8.5 to 9) conditions. The gels dried from the synthesized aluminosilicate sols were formed into a disk shape under 20 MPa pressure; then the green bodies were sintered for 3 h in the temperature range of 1100–1600 °C. The synthesizing temperature of mullite phase was found to be above 1200 °C for pH ≈ 1.5 to 2, and above 1300 °C for pH ≈ 4.5 to 5 and pH ≈ 8.5 to 9. The grain morphology of the synthesized mullite was changed to a rod shape for pH ≈ 1.5 to 2, and granulate shape for pH ≈ 4.5 to 5 and pH ≈ 8.5 to 9 with increasing sintering temperature. It was found that the morphology of mullite particle was predominantly governed by precursor pH and sintering temperature. However, at higher pH, the precursor pH and sintering temperature did not affect the synthesis behavior and grain morphology.

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Articles
Copyright
Copyright © Materials Research Society 2003

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References

REFERENCES

1.Dokko, P.C., Pask, J.A., and Nazdiyasni, K.S., J. Am. Ceram. Soc. 60, 150 (1997).CrossRefGoogle Scholar
2.Hirata, Y., Matsushita, S., Ishihara, Y., and Katsuki, H., J. Am. Ceram. Soc. 74, 2438 (1991).CrossRefGoogle Scholar
3.Aksay, I.A., Dabbs, D.M., and Sarikaya, M., J. Am. Ceram. Soc. 74, 2343 (1991).CrossRefGoogle Scholar
4.Klug, J. and Prochaka, S., J. Am. Ceram. Soc. 70, 750 (1987).CrossRefGoogle Scholar
5.Okada, K., Otsuka, N., and Somiya, S., Am. Ceram. Soc. Bull. 70, 1633 (1991).Google Scholar
6.Mah, T.I. and Mazdiyashi, K.S., J. Am. Ceram. Soc. 66, 699 (1983).CrossRefGoogle Scholar
7.Choi, Y.G., J. Kor. Ceram. Soc. 7, 773 (1999).Google Scholar
8.Hirata, Y., Sakeda, K., Matsuchma, Y., Shimada, K., and Ishihara, Y., J. Am. Ceram. Soc. 72, 995 (1989).CrossRefGoogle Scholar
9.Hoffman, D.W., Roy, R., and Komarneni, S., J. Am. Ceram. Soc. 67, 468 (1984).CrossRefGoogle Scholar
10.Jaymes, I., Douy, A., Massiot, D., and Coutures, J.P., J. Mater. Sci. 31, 4581 (1996).CrossRefGoogle Scholar
11.Rajendran, S., Rossell, H.J., and Sanders, J.V., J. Mater. Sci. 25, 4462 (1990).CrossRefGoogle Scholar
12.Chakraborty, A.K. and Ghosh, D.K., J. Mater. Sci. 29, 6131 (1994).CrossRefGoogle Scholar
13.Anilkumar, G.M., Mukundan, P., Damodaran, A.D., and Warrier, K.G.W., Mater. Lett. 33, 117 (1997).CrossRefGoogle Scholar
14.Okada, K. and Otuska, N., J. Am. Ceram. Soc. 74, 2414 (1991).CrossRefGoogle Scholar
15.Hong, J.S., Huang, X.X., and Guo, J.K., Mater. Lett. 24, 327 (1995).CrossRefGoogle Scholar
16.Song, K.C., Mater. Lett. 35, 290 (1998).CrossRefGoogle Scholar
17.Metcalfe, B.L. and Sant, J.H., Trans. J. Br. Ceram. Soc. 74(6), 193 (1995).Google Scholar
18.Ha, C.G., Jung, Y.G., Kim, J.W., Jo, C.Y., and Paik, U., Mater. Sci. & Eng. A 337, 212 (2002).CrossRefGoogle Scholar
19.Schneider, H., Okada, K., and Pask, J.A., Mullite and Mullite Ceramics (John Wiley & Sons, New York, 1994).Google Scholar
20.Temunjin, J., Okada, K., and Mackenzie, K.J.D., Ceram. Inter. 25, 85 (1999).CrossRefGoogle Scholar
21.Sacks, M.D., Lee, H.W., and Pask, J.A., in Mullite and Mullite Matrix Composites: A Review of Powder Preparation Methods and Densification Procedures for Fabricating High Density Mullite, edited by Somiya, S., Davis, R.F., and Pask, J.A. (Am. Ceram. Soc. Ceram. Trans. 61, Westerville, OH, 1990), pp. 167207.Google Scholar
22.Schneider, H., Voll, D., Merwin, L., and Sebald, A., J. Eur. Ceram. Soc. 11, 87 (1993).CrossRefGoogle Scholar
23.Okada, K. and Otsuka, N., in Mullite and Mullite Matrix Composites: Formation Process of Mullite, edited by Somiya, S., Davis, R.F., and Pask, J.A. (Am. Ceram. Soc. Ceram. Trans. 61, Westerville, OH, 1990), pp. 87375.Google Scholar
24.Ring, T.A., Fundamentals of Ceramic Powder Processing and Synthesis (Academic Press, New York, 1996), pp. 340347.Google Scholar
25.Chakravorty, A. and Ghosh, D.K., J. Am. Ceram. Soc. 71, 978 (1998).CrossRefGoogle Scholar