High-Temperature Oxidation Performance of Mo-Si-B Alloys: Current Results, Developments and Opportunities

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Abstract:

Ni-base superalloys are approaching the melting point as their fundamental limitation. For high-temperature components one possibility aiming at a further increase of efficiency, e.g. of jet turbines, is the use of refractory metals. Mo as base material is suitable for operating temperatures far beyond 1200°C. As a consequence of the formation of volatile Mo-oxides, it exhibits no intrinsic oxidation resistance when exceeding 700°C. Mo-Si-B alloys have melting points around 2000°C and retain good mechanical properties and oxidation resistance at very high temperatures. In air, the three-phase Mo-Si-B alloy dealt with in this paper shows excellent oxidation behaviour between 900°C-1300°C as a consequence of the formation of a protective silica scale. Below 900°C, alloys of this class suffer from catastrophic oxidation, leading to an evaporation of Mo-oxide and giving rise to a linear rate law of the weight loss. A protective oxide layer is not formed as a consequence of simultaneous and competitive Mo- and Si-oxide formation. Several approaches are possible to improve the oxidation performance of Mo-Si-B alloys, especially in this moderate temperature range. These include classical alloying, e.g. with Cr aiming for protective Cr-oxide scales, addition of small amounts of reactive elements for microstructure-refinement as well as selective oxidation of silica in oxygen-deficient atmospheres prior to operation in air. The results presented show promising opportunities and indicate that an oxidation protection from room temperature up to 1300°C requires a combination of the suggested approaches.

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587-592

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July 2011

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[1] D.M. Berczik, U.S. Patent no. 5, 595, 616, (East Hartford, United Technologies Corp., 1997).

Google Scholar

[2] D.M. Berczik, U.S. Patent no. 5, 693, 616, (East Hartford, United Technologies Corp., 1997).

Google Scholar

[3] S. Ochiai, Intermetallics 14, 1351 (2006).

Google Scholar

[4] S. Paswan, R. Mitra, and S. K. Roy, Intermetallics 15, 1217 (2007).

Google Scholar

[5] D. P. Whittle, J. Stringer, Phil. Trans. Roy. Soc. London A295, 309 (1980).

Google Scholar

[6] B. A. Pint, J. Am. Ceram. Soc. 86, 686 (2003).

Google Scholar

[7] F. Rioult, N. Sekido, R. Sakidja, and J. H. Perepezko, J. Electrochem. Soc. 154, C692 (2007).

DOI: 10.1149/1.2775164

Google Scholar

[8] H. Saage, M. Krüger, D. Sturm, M. Heilmaier, J.H. Schneibel, E. George, L. Heatherly, Ch. Somsen, G. Eggeler, Y. Yang, Acta Materialia 57, 13, (2009).

DOI: 10.1016/j.actamat.2009.04.040

Google Scholar