Add like
Add dislike
Add to saved papers

Oxidation Behavior of Refractory AlNbTiVZr 0.25 High-Entropy Alloy.

Materials 2018 December 13
Oxidation behavior of a refractory AlNbTiVZr0.25 high-entropy alloy at 600⁻900 °C was investigated. At 600⁻700 °C, two-stage oxidation kinetics was found: Nearly parabolic oxidation (n = 0.46⁻0.48) at the first stage, transitioned to breakaway oxidation (n = 0.75⁻0.72) at the second stage. At 800 °C, the oxidation kinetics was nearly linear (n = 0.92) throughout the entire duration of testing. At 900 °C, the specimen disintegrated after 50 h of testing. The specific mass gains were estimated to be 7.2, 38.1, and 107.5, and 225.5 mg/cm² at 600, 700, and 800 °C for 100 h, and 900 °C for 50 h, respectively. Phase compositions and morphology of the oxide scales were analyzed using X-ray diffraction (XRD) and scanning electron microscopy (SEM). It was shown that the surface layer at 600 °C consisted of the V₂O₅, VO₂, TiO₂, Nb₂O₅, and TiNb₂O₇ oxides. Meanwhile, the scale at 900 °C comprised of complex TiNb₂O₇, AlNbO₄, and Nb₂Zr₆O17 oxides. The oxidation mechanisms operating at different temperatures were discussed and a comparison of oxidation characteristics with the other alloys was conducted.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app