Abstract

Protective coatings for high temperature applications, as present e.g. during cutting and milling operations, require excellent mechanical and thermal properties during work load. The Ti1−xAlxN system is industrially well acknowledged as it covers some of these requirements, and even exhibits increasing hardness with increasing temperature in its cubic modification, known as age hardening. The thermally activated diffusion at high temperatures however enables for the formation of wurtzite AlN, which causes a rapid reduction of mechanical properties in Ti1−xAlxN coatings. The present work investigates the possibility to increase the formation temperature of w-AlN due to Hf alloying up to 10at.% at the metal sublattice of Ti1−xAlxN films. Ab initio predictions on the phase stability and decomposition products of quaternary Ti1−x−yAlxHfyN alloys, as well as the ternary Ti1−xAlxN, Hf1−xAlxN and Ti1−zHfzN systems, facilitate the interpretation of the experimental findings. Vacuum annealing treatments from 600 to 1100°C indicate that the isostructural decomposition, which is responsible for age hardening, of the Ti1−x−yAlxHfyN films starts at lower temperatures than the ternary Ti1−xAlxN coating. However, the formation of a dual phase structure of c-Ti1−zHfzN (with z=y/(1−x)) and w-AlN is shifted to ~200°C higher temperatures, thus retaining a film hardness of ~40GPa up to ~1100°C, while the Hf free films reach the respective hardness maximum of ~38GPa already at ~900°C. Additional annealing experiments at 850 and 950°C for 20h indicate a substantial improvement of the oxidation resistance with increasing amount of Hf in Ti1−x−yAlxHfyN.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.