Abstract

<p>In this paper, a comprehensive study on 1373 K high-temperature oxidation behaviors in a Ni-20 at.% Al-5 at.% Pt system was performed by coupling experimental investigations with CALPHAD (CALculation of PHAse Diagram) calculations. The discussion was expanded to include the effects of chemical concentrations on the degradation mechanism of thermally grown oxide layers during oxidation at 1373 K. A step-by-step oxidation procedure was established: first, aluminum oxide grows on the underside, followed by nickel oxide, which fully develops and penetrates the original aluminum oxide. The formation of NiO leads to aluminum enrichment and nickel depletion; once the concentration of Al achieves a threshold, θ-Al<sub>2</sub>O<sub>3</sub> transforms into α-Al<sub>2</sub>O<sub>3</sub>, forming a tight structure. At this point, Al diffusion toward the exterior predominates, followed by the inward diffusion of O. The diffusion of Ni is gradually restricted by the establishment of the α-Al<sub>2</sub>O<sub>3</sub> layer. When Al is not enough, Al<sub>2</sub>O<sub>3</sub> combines with NiO to develop NiAl<sub>2</sub>O<sub>4</sub>. Nickel segregation may also occur during subsequent oxidation at the oxide layer/matrix alloy boundary. Small voids are likely to form due to the merging of the vacancies caused by the unbalanced diffusion of Al toward the Al<sub>2</sub>O<sub>3</sub> layer and the opposite diffusion of Ni, resulting in significant peeling failure. Additionally, Pt has a beneficial effect by forming a thinner oxide scale that is more resistant to spallation.</p>

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.