Synthesis, Characterization and Sintering Behavior of Nanocrystalline Cordierite Ceramics

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Nanocrystalline cordierite powders were prepared by the polymerized complex method. The synthesized precursor was calcined in air at 600-1200 oC for 1h, and the calcined powders were fully characterized by TG/DTA, BET, XRD, SEM, and TEM. The XRD and selected-area electron diffraction (SAED) analysis confirmed the development of the phase composition of cordierite powders showing amorphous phase after calcination at temperature below 800oC, mixed phases of spinel and μ-cordierite phase after calcination at 800oC and 900oC, and mixed phases of spinel, μ- cordierite and α-cordierite phases after calcination at above 900oC. The BET specific surface areas of the calcined powders varied from 3 to 107 m2/g, depending on calcination temperature. The highest specific surface area of 107 m2/g was found in the powders calcined at 800oC. The average particle sizes evaluated by BET were less than 60 nm, depending on calcination temperature. The powders calcined at 800oC and 1000oC were uniaxially pressed and pressureless-sintered in air at 1250-1350oC for 2h. Densities of the sintered samples evaluated by Archimedes’s method were 87- 91 % of theoretical value. The crystal structure of all the sintered samples, determined by XRD, was mainly α-cordierite, having a small amount of spinel as second phase.

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242-247

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October 2006

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© 2006 Trans Tech Publications Ltd. All Rights Reserved

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[1] Y. Hirose, H. Doi, O. Kamigaito: J. Mater. Sci. Lett. Vol. 3 (1984), pp.153-55.

Google Scholar

[2] H. Ikawa et al.: J. Am. Ceram. Soc. Vol. 69(1986), pp.496-98.

Google Scholar

[3] B.P. Saha et al.: Materials Chemistry and Physics. Vol. 64(2001), pp.140-145.

Google Scholar

[4] C.D. Vogt, E. Ohara: Materials Aspects in Automotive Catalytic Converters. Wiley-VCH Verlag GmbH, Weinheim: 2002, pp.173-185.

Google Scholar

[5] T. Hamanaka, Handbook of Advanced Ceramics. Elsevier Academic Press, Oxford: 2003, pp.367-384.

Google Scholar

[6] K. Kata, Y. Shimada, H. Takamizawa: IEEE Trans. Compon. Hybrids. Manuf. Technol. Vol. 13 (1990), pp.448-451.

Google Scholar

[7] R. R. Tummala: J. Am. Ceram. Soc. Vol. 74 (1991), pp.895-908.

Google Scholar

[8] S. H. Knickerbocker, A. H. Kumer, L. W. Herron: Am. Ceram. Soc. Bull. Vol. 72(1993), p.9095.

Google Scholar

[9] S. J. Lee, W. M. Kriven: J. Am. Ceram. Soc. Vol. 81 (1998), pp.2605-12.

Google Scholar

[10] M. H. Nguyen, S. J. Lee, W.M. Kriven: J. Mater. Res. Vol. 14 (1999), pp.3417-26.

Google Scholar

[11] S. J. Lee, C. H. Lee, W. M. Kriven: J. Ceram. Proc. Res. Vol. 1 (2000), pp.92-95.

Google Scholar

[12] L. E. Chahal et. al.: J. Crystal Growth. Vol. 156 (1995), pp.99-107.

Google Scholar

[13] M. N. Rahaman. Ceramic processing and sintering. New York , Marcel Dekker, Inc.: (1995).

Google Scholar