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Fabrication of TiB2 and TiB2/FeB composites by mechanically activated borothermic reduction of ilmenite

Published online by Cambridge University Press:  31 January 2011

P. Millet*
Affiliation:
Department of Applied Mathematics and Electronic Materials Engineering, Research School of Physical Sciences and Engineering, The Australian National University, Canberra, ACT 0200, Australia
T. Hwang
Affiliation:
Department of Electronic Materials Engineering, Research School of Physical Sciences and Engineering, The Australian National University, Canberra, ACT 0200, Australia
*
a)Author to whom correspondence should be addressed. Present address: Centre d'Elaboration de Matiriaux et d'Etudes Structurales, CNRS, B.P. 4347, 29 rue Jeanne Marvig, 31055 Toulouse Cedex, France.
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Abstract

TiB2 and TiB2/FeB composites have been formed at temperatures below 1000 °C, directly from ilmenite sand by reaction with amorphous boron. The structural transformations occurring during high-energy mechanical milling pretreatment and subsequent annealing of different mixtures of the constituents have been studied. On heating at temperature below 800 °C, complete borothermic reduction of the ilmenite structure is accomplished. The mixture so obtained with an ilmenite-boron ratio equal to 1/6 undergoes a sequence of reactions on further heating to form TiB2, FeB, and the amorphous phase B2O2.

Type
Articles
Copyright
Copyright © Materials Research Society 1996

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References

REFERENCES

1.Terry, B. S. and Chinyamakobvu, O., Mater. Sci. Technol. 7, 842 (1991).Google Scholar
2.Low, I. M., J. Mater. Sci. Lett. 11, 715 (1992).CrossRefGoogle Scholar
3.Tkácová, K., Mechanical Activation of Minerals, Developments in Mineral Processing, edited by Fuerstenau, D. W. (Elsevier, Amsterdam, 1989), Vol. 11.Google Scholar
4.Popovich, A. A., Reva, V. P., and Vasilenko, V. N., J. Alloys Comp. 190, 143 (1993).CrossRefGoogle Scholar
5.Millet, P., Calka, A., and Ninham, B. W., J. Mater. Sci. Lett. 13, 1428 (1994).CrossRefGoogle Scholar
6.Millet, P. and Hwang, T., J. Mater. Sci. 31 (2), 351 (1996).CrossRefGoogle Scholar
7. Manufacturer: ANUtech Pty. Ltd., The Australian National University, Canberra, ACT 0200, Australia.Google Scholar
8.Jiang, Z. and Rhine, W. E., J. Eur. Ceram. Soc. 12, 403 (1993).CrossRefGoogle Scholar
9.Duncan, J. F. and Metson, J.B., NZ J. Sci. 25, 111 (1982).Google Scholar
10.Jing, J., Calka, A., and Camble, S. J., J. Phys. Condens. Matter 3, 7413 (1991).CrossRefGoogle Scholar