Hostname: page-component-7479d7b7d-qlrfm Total loading time: 0 Render date: 2024-07-11T20:24:17.206Z Has data issue: false hasContentIssue false

Intermediate-temperature oxidation behavior of Ti2AlC in air

Published online by Cambridge University Press:  31 January 2011

X. H. Wang
Affiliation:
High-Performance Ceramic Division, Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, 72 Wenhua Road, Shenyang, 110016, People's Republic of China
Y. C. Zhou*
Affiliation:
High-Performance Ceramic Division, Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, 72 Wenhua Road, Shenyang, 110016, People's Republic of China
*
a) Address all correspondence to this author. e-mail: yczhou@imr.ac.cn
Get access

Abstract

The isothermal oxidation behavior of Ti2AlC at intermediate temperatures of 500, 600, 700, 800, and 900 °C in flowing air was investigated by means of thermogravimetric analysis, x-ray diffraction (XRD), Raman spectroscopy, and scanning electron microscopy (SEM)/energy dispersive spectroscopy. An anomalous oxidation with higher kinetics at lower temperatures of 500 and 600 °C was observed although Ti2AlC exhibited good oxidation resistance at higher temperatures. As revealed by SEM scale morphology observation, oxidation-induced cracks present at temperatures of 500 and 600 °C resulted in poor protectivity of scales and accounted for the anomalous oxidation. The weight gain data for the remaining temperatures were analyzed with an instantaneous parabolic rate constant method by assuming a parabolic rate law. The variations of instantaneous parabolic rate constant with time reflected the complexity of the oxidation behavior of Ti2AlC at intermediate temperatures. These variations were discussed from the viewpoint of phase transformation of oxidation products on the basis of XRD, Raman spectroscopy, and SEM scale morphology observation. As indicated by XRD and Raman spectra, the scale formed on Ti2AlC at higher temperature was stable α–Al2O3 and rutile TiO2, while transition aluminas of γ–Al2O3, δ–Al2O3, θ–Al2O3, and TiO2 (anatase) were detected at lower temperatures. The whisker morphology of θ–Al2O3 at 800 °C and ridged morphology of α–Al2O3 at 800 and 900 °C were confirmed by SEM.

Type
Articles
Copyright
Copyright © Materials Research Society 2002

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

REFERENCES

1.Jeitschko, W., Nowotny, H., and Benesovky, F., Monatsh. Chem. 94, 672 (1963).CrossRefGoogle Scholar
2.Pietzka, M.A. and Schuster, J.C., J. Phase Equilib. 15, 392 (1994).CrossRefGoogle Scholar
3.Barsoum, M.W., Brodkin, D., and El-Raghy, T., Scr. Mater. 36, 535 (1997).CrossRefGoogle Scholar
4.Barsoum, M.W., Ali, M., and El-Raghy, T., Metall. Mater. Trans. A. 31, 1857 (2000).CrossRefGoogle Scholar
5.Wang, X.H. and Zhou, Y.C., Z. Metallkd. 93, 66 (2002).Google Scholar
6.Zhou, Y.C. and Wang, X.H., Mat. Res. Innovations 5, 87 (2001).CrossRefGoogle Scholar
7.Wang, X.H. and Zhou, Y.C., Oxid. Met. (in press).Google Scholar
8.Roy, T.K., Blasubramaniam, R., and Gosh, A., Metall. Mater. Trans. A. 27, 3993 (1996).CrossRefGoogle Scholar
9.Mungole, M.N., Blasubramaniam, R., and Gosh, A., Intermetallics 8, 717 (2000).CrossRefGoogle Scholar
10.Schaeffer, J.C., Scr. Metall. Mater. 28, 791 (1993).CrossRefGoogle Scholar
11.Babu, N., Balasubramaniam, R., and Ghosh, A., Corros. Sci. 43, 2239 (2001).CrossRefGoogle Scholar
12.Ohsaka, T., Izumi, F., and Fujiki, Y., J. Raman Spectrosc. 7, 321 (1978).CrossRefGoogle Scholar
13.Balachandran, U. and Eror, N.G., J. Solid State Chem. 42, 276 (1982).CrossRefGoogle Scholar
14.Turkovic, A., Ivanda, M., Vranesa, V., and Drasner, A., Vacuum 43, 471 (1992).CrossRefGoogle Scholar
15.Lottici, P.P., Bersani, D., Braghini, M., and Montenero, A., J. Mater. Sci. 28, 177 (1993).CrossRefGoogle Scholar
16.Iida, Y., Furukawa, M., Aoki, T., and Sakai, T., Appl. Spectrosc. 52, 673 (1998).CrossRefGoogle Scholar
17.Porto, S.P.S., Fleury, P.A., and Damen, T.C., Phys. Rev. 154, 522 (1967).CrossRefGoogle Scholar
18.Aminzadeh, A., Appl. Spectrosc. 51, 817 (1997).CrossRefGoogle Scholar
19.Shimada, S. and Kozeki, M., J. Mater. Sci. 27, 1869 (1992).CrossRefGoogle Scholar
20.Racault, C., Langlais, F., and Naslain, R., J. Mater. Sci. 29, 3384 (1994).CrossRefGoogle Scholar
21.Wang, X.H. and Zhou, Y.C., J. Mater. Chem. 12, 2781 (2002).CrossRefGoogle Scholar
22.Zhou, Y.C. and Sun, Z.M., Phys. Rev. B 61, 12570 (2000).CrossRefGoogle Scholar
23.Rommerskirchen, I., Eltester, B., and Grabke, H.J., Mater. Corros. 47, 646 (1996).CrossRefGoogle Scholar
24.Doychak, J., in Intermetallic Compounds, edited by Westbrook, J.H. and Fleischer, R.L. (Wiley, New York, 1994), p. 977.Google Scholar