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Thermal Expansion of Ti5Si3 with Ge, B, C, N, or O Additions

Published online by Cambridge University Press:  31 January 2011

J. J. Williams
Affiliation:
Ames Laboratory and Department of Materials Science and Engineering, Iowa State University, Ames, Iowa 50011
M. J. Kramer
Affiliation:
Ames Laboratory and Department of Materials Science and Engineering, Iowa State University, Ames, Iowa 50011
M. Akinc
Affiliation:
Ames Laboratory and Department of Materials Science and Engineering, Iowa State University, Ames, Iowa 50011
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Abstract

The crystallographic thermal expansion coefficients of Ti5Si3 from 20 to 1000 °C as a function of B, C, N, O, or Ge content were measured by high-temperature x-ray diffraction using synchrotron sources at Cornell University (Cornell High Energy Synchrotron Source; CHESS) and Argonne National Laboratory (Advanced Photon Source; APS). Whereas the ratio of the thermal expansion coefficients along the c and a axes was approximately 3 for pure Ti5Si3, this ratio decreased to about 2 when B, C, or N atoms were added. Additions of O and Ge were less efficient at reducing this thermal expansion anisotropy. The extent by which the thermal expansion was changed when B, C, N, or O atoms were added to Ti5Si3 correlated with their expected effect on bonding in Ti5Si3.

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Articles
Copyright
Copyright © Materials Research Society 2000

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References

REFERENCES

1.Thom, A.J. and Akinc, M., in Advanced Ceramics for Structural and Tribological Applications, edited by Hawthorne, H.M. and Troczynski, T. (Metallurgical Society of Canadian Institute of Mining, Metallurgy and Petroleum International Symposium Proceedings, Vancouver, BC, Canada, 1995), p. 619.Google Scholar
2.Zhang, L. and Wu, J., Scripta Mater. 38, 307 (1998).CrossRefGoogle Scholar
3.Ikarashi, Y., Ishizaki, K., Nagai, T., Hashizuka, Y., and Kondo, Y., Intermetallics 4, 141 (1996).CrossRefGoogle Scholar
4.Thom, A.J., Akinc, M., Cavin, O.B., and Hubbard, C.R., J. Mater. Sci. Lett. 13, 1657 (1994).CrossRefGoogle Scholar
5.Nakashima, T. and Umakoshi, Y., Philos. Mag. Lett. 66, 317 (1992).Google Scholar
6.Thom, A.J., Young, V.G., and Akinc, M., J. Alloys Compds. 296, 59 (2000).CrossRefGoogle Scholar
7.Williams, J.J., Kramer, M.J., Akinc, M. and Malik, S.K., J. Mater. Res. 15, 99335 (2000).Google Scholar
8.Kim, Y., Thom, A.J., and Akinc, M., in Processing and Fabrication of Advanced Materials for High Temperature Applications–II, edited by Srivatsan, T.S. and Ravi, V.A. (The Minerals, Metals and Materials Society Symposium Proceedings, Warrendale, PA, 1992), p. 189.Google Scholar
9.Margulies, L., Kramer, M.J., Williams, J.J., Deters, E.M., McCallum, R.W., Haeffner, D.R., Lang, J.C., Kycia, S., and Goldman, A.I., in Applications of Synchrotron Radiation Techniques to Materials Science IV, edited by Mini, S.M., Stock, S.R., Perry, D.L., and Terminello, L.J. (Mater. Res. Soc. Symp. Proc. 524, Warrendale, PA, 1998), p. 139.Google Scholar
10.Margulies, L., Kramer, M.J., McCallum, R.W., Kycia, S., Haeffner, D.R., Lang, J.C., and Goldman, A.I., Rev. Sci. Instrum. 70, 3554 (1999).CrossRefGoogle Scholar
11.Appleman, D.E. and Evans, H.T., U.S. National Technical Information Service, Document No. PB2–16188 (1973).Google Scholar
12.Carbide, Nitride and Boride Synthesis and Processing, edited by A.W. Weimer (Chapman and Hall, London, 1997), p. 646.Google Scholar
13.Hashin, Z., J. Mech. Phys. Solids 32, 149 (1984).CrossRefGoogle Scholar
14.Mitra, R., Metall. Mater. Trans. A 29, 1629 (1998).CrossRefGoogle Scholar
15.Rosenkranz, R., Frommeyer, G., and Smarsly, W., Mater. Sci. Eng., A 152, 288 (1992).CrossRefGoogle Scholar