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Powder synthesis of barium titanate and barium orthotitanate via an ethylene glycol complex polymerization route

Published online by Cambridge University Press:  31 January 2011

S. J. Lee ,
M. D. Biegalski  and
W. M. Kriven
S. J. Lee
Affiliation:
Department of Materials Science and Engineering, University of Illinois at Urbana–Champaign, Urbana, Illinois 61801
M. D. Biegalski
Affiliation:
Department of Materials Science and Engineering, University of Illinois at Urbana–Champaign, Urbana, Illinois 61801
W. M. Kriven
Affiliation:
Department of Materials Science and Engineering, University of Illinois at Urbana–Champaign, Urbana, Illinois 61801
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Abstract

Pure and reactive barium titanate (BaTiO3) and barium orthotitanate (Ba2TiO4) powders have been synthesized by an ethylene glycol (EG), polymerizationcomplexation route. The EG content affected the crystallization behavior and powder morphology. The BaTiO3powder, which had a particle size of approximately 100 nm, crystallized from amorphous to tetragonal phase on calcining at 700 °C for 1 h. Ball-milled BaTiO3 powder sintered to 97% relative density at 1200 °C after 2 h, with a grain size of approximately 200 nm. Ba2TiO4 powder required longer holding times or higher temperatures to be crystallized from the amorphous phase than did BaTiO3. In Ba2TiO4, the phase transformation between low-temperature monoclinic symmetry to high-temperature orthorhombic symmetry was observed by dilatometry and differential scanning calorimetry. A volume decrease of ∼0.5% accompanied the monoclinic-to-orthorhombic transformation on heating. The high-temperature orthorhombic phase could be retained down to room temperature y the addition of at least 6 wt% magnesia (MgO) stabilizer.

Type
Articles
Information
Journal of Materials Research , Volume 14 , Issue 7 , July 1999 , pp. 3001 - 3006
Copyright
Copyright © Materials Research Society 1999

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References

REFERENCES

1.Moulson, A.J. and Herbert, J.M., Electroceramics (Chapman & Hall, London, 1990).Google Scholar
2.Kumazawa, H., Kagimoto, T., and Kawabata, A., J. Mater. Sci 31, 2599 (1996).CrossRefGoogle Scholar
3.Yao, K., Zang, L., Yao, X., and Zhu, W., J. Mater. Sci. 32, 3659 (1997).CrossRefGoogle Scholar
4.Arima, M., Kakihana, M., Nakamura, Y., Yashima, M., and Yoshimura, M., J. Am. Ceram. Soc. 79, 2847 (1996).CrossRefGoogle Scholar
5.Godbole, P.D., Deshpande, S.B., Potdar, H.S., and Date, S.K., Mater. Lett. 12, 97 (1991).CrossRefGoogle Scholar
6.Kim, S., Lee, M., Noh, T., and Lee, C., J. Mater. Sci. 31, 3643 (1996).CrossRefGoogle Scholar
7.Rase, D.E. and Roy, R., J. Am. Ceram. Soc. 38, 108 (1955).Google Scholar
8.Ritter, J.J., Roth, R.S., and Blendell, J.E., J. Am. Ceram. Soc. 69, 155 (1986).CrossRefGoogle Scholar
9.Bland, J.A., Acta. Cryst. 14, 875 (1961).CrossRefGoogle Scholar
10.Todd, S.S. and Lorenson, R.E., J. Am. Chem. Soc. 74, 3764 (1953).CrossRefGoogle Scholar
11.Nguyen, M.H., Masters thesis, University of Illinois at Urbana-Champaign, (1997).Google Scholar
12.Mazdiyasni, K.S., Dolloff, R.T., and Smith, J.S., J. Am. Ceram. Soc. 52, 523 (1969).CrossRefGoogle Scholar
13.Alcock, J.R., Riley, F.L., D'Angeli, C., and Thomas, A.G., Br. Ceram. Trans. J. 90, 152 (1991).Google Scholar
14.Pechini, M.P., U.S. Patent No. 3 330 697 (1967).Google Scholar
15.Gülgün, M.A., Popoola, O.O., and Kriven, W.M., J. Am. Ceram. Soc. 77, 531 (1994).CrossRefGoogle Scholar
16.Budd, D. and Payne, D.A., in Better Ceramics Through Chemistry, edited by Brinker, C.J., Clark, D.E., and Ulrich, D.R. (Mater. Res. Soc. Symp. Proc. 32, Elsevier Science Publishing, New York, 1984), p. 239.Google Scholar
17.Tai, L.W. and Lessing, P.A., J. Mater. Res. 7, 502 (1992).CrossRefGoogle Scholar
18.Jonker, G.H. and Kwestroo, W., J. Am. Ceram. Soc. 41, 390 (1958).CrossRefGoogle Scholar
19.Gülgün, M.A., Nguyen, M.H., and Kriven, W.M., J. Am. Ceram. Soc. 82, 556 (1999).CrossRefGoogle Scholar
20.Nguyen, M.H., Lee, S.J., and Kriven, W.M., J. Mater. Res. (1999, in press)Google Scholar
21.Sun, Y.N., Sacks, M.D., and Williams, J.W., in Ceramic Transactions, Vol. 1, edited by Messing, G.L., Fuller, E.R. Jr, and Hausner, H. (The American Ceramic Society, Westerville, OH, 1988), pp. 538–548.Google Scholar
22.Shin, W.K., Sacks, M.D., Scheiffle, G.W., and Williams, J.W., in Ceramic Transactions, Vol. 1, edited by Messing, G.L., Fuller, E.R. Jr, and Hausner, H. (The American Ceramic Society, Westerville, OH, 1988), pp. 549–558.Google Scholar
23.Proust, C., Miot, C., and Husson, E., Ferroelectrics 186, 89 (1996).CrossRefGoogle Scholar
24.Arend, H. and Kihlborg, L., J. Am. Ceram. Soc. 52, 63 (1969).CrossRefGoogle Scholar