Hostname: page-component-76fb5796d-dfsvx Total loading time: 0 Render date: 2024-04-26T11:17:23.432Z Has data issue: false hasContentIssue false

The Effect of Cooling Rate During Rapid Solidification on the Structure and Texture of NiTi

Published online by Cambridge University Press:  28 February 2011

A. J. Pedraza
Affiliation:
Department of Materials Science and Engineering, The University of Tennessee, Knoxville, TN 37996-2000
M. J. Godbole
Affiliation:
Department of Materials Science and Engineering, The University of Tennessee, Knoxville, TN 37996-2000
E. A. Kenik
Affiliation:
Metals and Ceramics Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831-6376
D. F. Pedraza
Affiliation:
Metals and Ceramics Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831-6376
D. H. Lowndes
Affiliation:
Solid State Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831-6056
Get access

Abstract

A study has been conducted on the effects of increasing cooling rate during rapid solidification of NiTi upon the phases that are produced. The hammer and anvil rapid solidification technique and laser melting with a nanosecond excimer laser were used, which allow the cooling rate to be varied by three to four orders of magnitude. Although 1/3 {110} superlattice reflections are seen in the selected area diffraction (SAD) patterns of the splat quenched (SQ) specimens, x-ray diffraction analyses show the presence of only B2 phase and martensite. On the other hand, laser treatment (LT) of the specimens produces a layer that has a L10 structure with a slight monoclinic distortion. This phase can be envisaged as a small distortion of a B2 unit cell with a volume per atom ~3.3% lower than the equilibrium B2 phase. Also martensite is present in the layer. SQ alloys exhibit a marked {200} texture due to columnar growth opposite to the direction of heat extraction, while LT produces epitaxial regrowth of the melted layer. No substantial disordering is obtained in NiTi rapidly solidified alloys.

Type
Articles
Copyright
Copyright © Materials Research Society 1987

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Sandrock, G. D., Perkins, A. J., and Hehemann, R. F., Met. Trans. 2, 2769 (1971)CrossRefGoogle Scholar
2. Wang, F. E., Buehler, W. J., and Pickart, S. J., J. Appl. Phys. 36, 3232 (1965)Google Scholar
3. Ling, H. C. and Kaplow, R., Met Trans. 11A, (1979) 77 Google Scholar
4. Dautovich, D. P. and Purdy, G. R., Can. Metall. Quart. 4, 129 (1965).Google Scholar
5. Hwang, C. M., M.Meichle, C., Salamon, M. B., and Wayman, C. M., (a) Phil. Mag. A 47,9 (1983); (b)ib, A47, 31 (1983).Google Scholar
6. Goo, E. and Sinclair, R., Acta Metall 33, 1717 (1985).Google Scholar
7. Tietze, H., Mullner, M., Selgert, P., and Assmus, W., J. Phys. F: Met. Phys. 15, 263 (1985).Google Scholar
8. Shabalovskaya, S. A., Lotkov, A. I., and Baturin, A. A., Phys. Met. Metall. 56, 67 (1983).Google Scholar
9. Buschow, K. H. J., J. Phys. F: Met. Phys. 13, 563 (1983).Google Scholar
10. Philip, T. V. and Beck, P. A., Trans. AIME 221, 1269 (1957); P. Villars and L. D. Calvert, ”Pearson's Handbook of Crystallographic Data for Intermetallic Phases”, Volume 3, p. 2905 (American Society for Metals, 1985)Google Scholar
11. McCamy, J. W., Godbole, M. J., Lowndes, D. H. and Pedraza, A. J., J. Mater. Res. 1, 629 (1986).Google Scholar