Abstract
The 700°C isothermal section of the Fe–Cr–Si ternary phase diagram has been determined experimentally by means of scanning electron microscopy coupled with energy dispersive X-ray spectroscopy and X-ray powder diffraction. Ten three-phase regions exist in the 700°C isothermal section. The binary σ phase contains 0–17.6 at.% Si and 31.4–59.2 at.% Cr; the Fe5Si3 phase is stable at 700°C because of the dissolution of Cr. At this temperature, Fe and Cr cannot be entirely substituted by each other to form the FeSi or CrSi phases: the maximum possible Cr content in FeSi2, Fe5Si3 and D03 is 3.9, 20.7 and 15.2 at.%, respectively, and the maximum soluble Fe in CrSi2, Cr5Si3 and Cr3Si is 2.5, 20.4 and 16.8 at.%, respectively.
References
[1] K.Yamamoto, Y.Kimura, Y.Mishima: Scr. Mater. 50 (2004) 977. 10.1016/j.scriptamat.2004.01.006Search in Google Scholar
[2] P.J.Cunat: Alloying Elements in Stainless Steel and Other Chromium-Containing Alloys, Int. Chromium Dev. Assoc.Paris, (2004).Search in Google Scholar
[3] J.Robertson, M.I.Manning: J. Mater. Sci. Technol. 5 (1989) 741. 10.1179/026708389790222825Search in Google Scholar
[4] Z.Zhou, Z.Li, X.M.Wang, Y.X.Liu, Y.Wu, M.X.Zhao, F.C.Yin: Thermochim. Acta. 577 (2014) 59. 10.1016/j.tca.2013.12.009Search in Google Scholar
[5] A.G.H.Andersen, E.R.Jette: Trans. Amer. Soc. Met. 24 (1936) 375.Search in Google Scholar
[6] E.I.Gladyshevsky, L.K.Borusevich: Izv. Akad. Nauk SSSR, Met. 1 (1966) 159.Search in Google Scholar
[7] V.Raghavan: Phase diagrams of ternary iron alloys, Part 1, ASM International, Materials Park, Ohio, 11 (1987) 31.Search in Google Scholar
[8] M.Lindholm: J. Phase Equilib. 18 (1997) 432. 10.1007/BF02647699Search in Google Scholar
[9] Y.Dusausoy, J.Protas: Acta Crystallogr. 27 (1971) 1209. 10.1107/S0567740871003765Search in Google Scholar
[10] R.Wartchow, S.Gerighausen, M.Binnewies: Z. Kristallogr. 212 (1997) 320. 10.1524/zkri.1997.212.1.57Search in Google Scholar
[11] D.Errandonea, D.Santamaría–Perez, A.Vegas, J.Nuss, M.Jansen, P.Rodríguez–Hernandez, A.Muñoz: Phys. Rev. B77 (2008) 094113–1. 10.1103/PhysRevB.77.045208Search in Google Scholar
[12] M.Schuette, R.Wartchow, M.Binnewies: Z. Anorg. Allg. Chem. 629 (2003) 1846. 10.1002/zaac.200300125Search in Google Scholar
[13] T.Dasgupta, J.Etourneau, B.Chevalier, S.F.Matar, A.M.Umarji: J. Appl. Phys. 103 (2008) 113516–1. 10.1063/1.2917347Search in Google Scholar
[14] W.Jauch, A.J.Schultz, G.Heger: J. Appl. Crystallogr. 20 (1987) 117. 10.1107/S0021889887086400Search in Google Scholar
[15] C.H.Dauben, D.H.Templeton, C.E.Myers: J. Phys. Chem. 60 (1956) 443. 10.1021/j150538a015Search in Google Scholar
[16] B.Altintas: J. Phys. Chem. Solids72 (2011) 1325. 10.1016/j.jpcs.2011.07.027Search in Google Scholar
[17] V.Raghavan: J. Phase Equilib. 24 (2003) 265. 10.1007/s11669-003-0009-1Search in Google Scholar
[18] O.Kubaschewski: Iron Binary Phase Diagrams, Springer, Berlin (1982).Search in Google Scholar
[19] S.Ackerbauer, N.Krendelsberger, F.Weitzer, K.Hiebl, J.C.Schuster: Intermetallics17 (2009) 414. 10.1016/j.intermet.2008.11.016Search in Google Scholar
© 2014, Carl Hanser Verlag, München