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Oxidation resistance of Ti <sub>3</sub> AlC <sub>2</sub> and Ti <sub>3</sub> Al <sub>0.8</sub> Sn <sub>0.2</sub> C <sub>2</sub> MAX phases: A comparison

Élodie DrouelleInstitut PPRIME CNRS Université de Poitiers/ENSMA UPR 3346 CNRS Chasseneuil du Poitou‐Futuroscope Cedex FranceVéronique Gauthier‐BrunetInstitut PPRIME CNRS Université de Poitiers/ENSMA UPR 3346 CNRS Chasseneuil du Poitou‐Futuroscope Cedex FranceJonathan CormierInstitut PPRIME CNRS Université de Poitiers/ENSMA UPR 3346 CNRS Chasseneuil du Poitou‐Futuroscope Cedex FrancePatrick VillechaiseInstitut PPRIME CNRS Université de Poitiers/ENSMA UPR 3346 CNRS Chasseneuil du Poitou‐Futuroscope Cedex FrancePierre SallotSafran Tech Magny les hameaux Cedex FranceFoad NaïmiLaboratoire Interdisciplinaire Carnot de Bourgogne UMR 6303 CNRS‐Université de Bourgogne Franche‐Comté DIJON Cedex FranceFrédéric BernardLaboratoire Interdisciplinaire Carnot de Bourgogne UMR 6303 CNRS‐Université de Bourgogne Franche‐Comté DIJON Cedex FranceS. DuboisInstitut PPRIME CNRS Université de Poitiers/ENSMA UPR 3346 CNRS Chasseneuil du Poitou‐Futuroscope Cedex France
2019en
ABI

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Abstract Ti 3 AlC 2 and Ti 3 Al 0.8 Sn 0.2 C 2 MAX phase powders are densified using Spark Plasma Sintering (SPS) technique to obtain dense bulk materials. Oxidation tests are then performed over the temperature range 800°C‐1000°C under synthetic air on the two different materials in order to compare their oxidation resistance. It is demonstrated that, in the case of the Ti 3 Al 0.8 Sn 0.2 C 2 solid solution, the oxide layers consist in TiO 2 , Al 2 O 3 , and SnO 2 . The presence of Sn atoms in the A planes of the solid solution leads to an easy diffusion of Sn out of the MAX phase which promote the formation of the nonprotective and fast growing SnO 2 oxide. Moreover, the small Al/Ti atom's ratio promotes the growth of a nonprotective rutile‐TiO 2 scale as well. In the case of the Ti 3 AlC 2 MAX phase, the oxide layer consists in a protective alumina scale; a few TiO 2 grains being observed on the top of the Al 2 O 3 layer. The parabolic oxidation rate constants are about 3 orders of magnitude smaller for Ti 3 AlC 2 compared to Ti 3 Al 0.8 Sn 0.2 C 2 .

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