{"title":"Effect of oxidation time on the composition and structure evolution of the oxide film on Al-Mg-Sc-Zr alloy","authors":"Mingjin Wu","doi":"10.1016/j.vacuum.2025.114359","DOIUrl":null,"url":null,"abstract":"<div><div>The oxidation behavior of Al-Mg-Sc-Zr alloy at 300 °C for different oxidation times was systematically studied, the influence of oxidation time on the composition of the oxide scale and the microstructure of the substrate was revealed, and the relationship between oxidation time, microstructure of substrate and oxide scale composition and structure was established. The results showed that with the increase of oxidation time, the morphology of the oxide scale changed from irregular and thin film to a loose structure oxide scale with MgO particle aggregates, and finally formed a thick and dense oxide scale. Initially, Al<sub>2</sub>O<sub>3</sub> dominated the oxide scale composition, but with increasing oxidation time, the MgO content gradually increased. At 1.5h, the MgO content in the oxide scale exceeded that of Al<sub>2</sub>O<sub>3</sub>, eventually becoming the predominant component. And at 2.0 h, the composition of the oxide scale changed to MgO, MgAl<sub>2</sub>O<sub>4</sub>, and a few Al<sub>2</sub>O<sub>3</sub>, and MgAl<sub>2</sub>O<sub>4</sub> was present largely in the deep part of the oxide scale, gradually replacing MgO in the thickness direction as the oxidation time prolonged. At the same time, the orientation of the matrix grains changed, and the proportion of HAGBs increased dramatically, which increased the diffusion rate of Mg atoms. As the oxidation time increased, changes in dislocation density and precipitation of nanoparticles also affected the path and speed of atomic migration, thereby determining the phase composition and structural stability of the oxide scale on Al-Mg-Sc-Zr alloy.</div></div>","PeriodicalId":23559,"journal":{"name":"Vacuum","volume":"239 ","pages":"Article 114359"},"PeriodicalIF":3.8000,"publicationDate":"2025-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Vacuum","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0042207X25003495","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The oxidation behavior of Al-Mg-Sc-Zr alloy at 300 °C for different oxidation times was systematically studied, the influence of oxidation time on the composition of the oxide scale and the microstructure of the substrate was revealed, and the relationship between oxidation time, microstructure of substrate and oxide scale composition and structure was established. The results showed that with the increase of oxidation time, the morphology of the oxide scale changed from irregular and thin film to a loose structure oxide scale with MgO particle aggregates, and finally formed a thick and dense oxide scale. Initially, Al2O3 dominated the oxide scale composition, but with increasing oxidation time, the MgO content gradually increased. At 1.5h, the MgO content in the oxide scale exceeded that of Al2O3, eventually becoming the predominant component. And at 2.0 h, the composition of the oxide scale changed to MgO, MgAl2O4, and a few Al2O3, and MgAl2O4 was present largely in the deep part of the oxide scale, gradually replacing MgO in the thickness direction as the oxidation time prolonged. At the same time, the orientation of the matrix grains changed, and the proportion of HAGBs increased dramatically, which increased the diffusion rate of Mg atoms. As the oxidation time increased, changes in dislocation density and precipitation of nanoparticles also affected the path and speed of atomic migration, thereby determining the phase composition and structural stability of the oxide scale on Al-Mg-Sc-Zr alloy.
期刊介绍:
Vacuum is an international rapid publications journal with a focus on short communication. All papers are peer-reviewed, with the review process for short communication geared towards very fast turnaround times. The journal also published full research papers, thematic issues and selected papers from leading conferences.
A report in Vacuum should represent a major advance in an area that involves a controlled environment at pressures of one atmosphere or below.
The scope of the journal includes:
1. Vacuum; original developments in vacuum pumping and instrumentation, vacuum measurement, vacuum gas dynamics, gas-surface interactions, surface treatment for UHV applications and low outgassing, vacuum melting, sintering, and vacuum metrology. Technology and solutions for large-scale facilities (e.g., particle accelerators and fusion devices). New instrumentation ( e.g., detectors and electron microscopes).
2. Plasma science; advances in PVD, CVD, plasma-assisted CVD, ion sources, deposition processes and analysis.
3. Surface science; surface engineering, surface chemistry, surface analysis, crystal growth, ion-surface interactions and etching, nanometer-scale processing, surface modification.
4. Materials science; novel functional or structural materials. Metals, ceramics, and polymers. Experiments, simulations, and modelling for understanding structure-property relationships. Thin films and coatings. Nanostructures and ion implantation.