Abstract

The long-term isothermal oxidation behavior of bulk Ti2AlC in air and 100% water vapor has been investigated in the 1000–1300°C temperature range. The kinetics, for oxidation up to 120 hours, follows a cubic rate law in both environments – air and water vapor. The kinetics was found to be slightly faster for hydrothermal oxidation compared to oxidation in air, especially below 1100°C. However, there is little variation between the activation energies for oxidation in air (approximately 279 kJ/m3) and in 100% water vapor (approximately 261 kJ/m3). Scanning electron microscopy, energy dispersive spectroscopy and X-ray diffraction show that oxidation of Ti2AlC forms mostly a continuous and stable layer of α-Al2O3, along with a thin surface layer of rutile-TiO2 in both environments. However, the thin TiO2 layer volatilizes by forming gaseous TiO(OH)2 in the presence of water vapor at high temperatures (>1200°C). At short-term oxidation and lower temperatures, diffusion of hydroxyl ions is proposed to be the rate limiting mechanism under hydrothermal conditions. Above 1100°C, the diffusion of oxide ions through Al2O3 layer becomes the rate limiting step and humidity has little effect on the overall oxidation kinetics of Ti2AlC.

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