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Comparison of Different Fluorine-treatments for Improved High Temperature Oxidation Resistance of TiAl-alloys
Published online by Cambridge University Press: 07 March 2011
Abstract
Intermetallic TiAl-alloys can replace the heavier Ni-based superalloys in several high temperature applications with regards to their mechanical properties, however they can not be used at temperatures above 800°C in oxidizing environments for longer times because of insufficient oxidation resistance. Despite an Al-content of about 45 at.% in technical alloys, no protective alumina layer is formed because the thermodynamic stabilities of titanium oxide and aluminum oxide are of the same order of magnitude. Therefore a mixed TiO2/Al2O3-scale is formed which is fast growing so that the metal consumption rate is quite high. On the other hand the formation of a slow growing alumina layer is promoted by a fluorine treatment. This so called fluorine effect leads to the preferential intermediate formation of gaseous aluminum fluorides at elevated temperatures if the fluorine content at the surface stays within a defined concentration range. These fluorides are converted into solid Al2O3 due to the high oxygen partial pressure of the high temperature service environment forming a protective pure Al2O3 surface scale. In this paper results of high temperature oxidations tests of several technical TiAl-alloys will be presented. Different F-treatments e.g. dipping or spaying which are easy to apply have been used and their results will be compared. The mass change data of the F-treated specimens are always lower than those of the untreated ones. Post experimental investigations such as light microscopy, scanning electron microscopy and energy dispersive X-ray analysis reveal the formation of a thin alumina layer on the F-treated samples after optimization of the process while a thick mixed scale is found on the untreated samples. The results will be discussed in view of an optimized procedure and the future use of TiAl-components in high temperature environments.
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- Copyright © Materials Research Society 2011