{"title":"Re-investigation of the Phase Equilibria and Thermodynamic Assessment of the Mg-Sm Binary System","authors":"Ruyi Jiang, Xiaofen Duan, Dashi Li, Cuiyun He","doi":"10.1007/s11669-024-01111-0","DOIUrl":null,"url":null,"abstract":"<div><p>The Mg-Sm phase diagram has been experimentally studied by x-ray diffraction, scanning electron microscope equipped with energy dispersive spectrometer, and differential scanning calorimetry. Five binary compounds, Mg<sub>41</sub>Sm<sub>5</sub>, Mg<sub>5</sub>Sm, Mg<sub>3</sub>Sm, Mg<sub>2</sub>Sm and MgSm were confirmed to exist in the Mg-Sm system. In addition to Mg<sub>2</sub>Sm and MgSm, Mg<sub>3</sub>Sm was found to be a congruently melting phase. The Mg<sub>5</sub>Sm and Mg<sub>2</sub>Sm were found to be only stable at high temperatures and decompose above 400 °C in this work. A special effort was made to determine the extent of the solid solubility ranges of Mg<sub>3</sub>Sm, Mg<sub>2</sub>Sm, MgSm and, <i>γ</i>-Sm. The Mg-Sm binary system was modeled using the Calphad approach based on new experimental data of this work and all reliable experimental information from literature. A complete thermodynamic description of the Mg-Sm system is obtained and extensive comparisons between calculated and experimental data are presented, indicating that almost all available experimental and theoretical data are fitted satisfactorily.</p></div>","PeriodicalId":657,"journal":{"name":"Journal of Phase Equilibria and Diffusion","volume":"45 3","pages":"520 - 536"},"PeriodicalIF":1.5000,"publicationDate":"2024-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Phase Equilibria and Diffusion","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s11669-024-01111-0","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The Mg-Sm phase diagram has been experimentally studied by x-ray diffraction, scanning electron microscope equipped with energy dispersive spectrometer, and differential scanning calorimetry. Five binary compounds, Mg41Sm5, Mg5Sm, Mg3Sm, Mg2Sm and MgSm were confirmed to exist in the Mg-Sm system. In addition to Mg2Sm and MgSm, Mg3Sm was found to be a congruently melting phase. The Mg5Sm and Mg2Sm were found to be only stable at high temperatures and decompose above 400 °C in this work. A special effort was made to determine the extent of the solid solubility ranges of Mg3Sm, Mg2Sm, MgSm and, γ-Sm. The Mg-Sm binary system was modeled using the Calphad approach based on new experimental data of this work and all reliable experimental information from literature. A complete thermodynamic description of the Mg-Sm system is obtained and extensive comparisons between calculated and experimental data are presented, indicating that almost all available experimental and theoretical data are fitted satisfactorily.
期刊介绍:
The most trusted journal for phase equilibria and thermodynamic research, ASM International''s Journal of Phase Equilibria and Diffusion features critical phase diagram evaluations on scientifically and industrially important alloy systems, authored by international experts.
The Journal of Phase Equilibria and Diffusion is critically reviewed and contains basic and applied research results, a survey of current literature and other pertinent articles. The journal covers the significance of diagrams as well as new research techniques, equipment, data evaluation, nomenclature, presentation and other aspects of phase diagram preparation and use.
Content includes information on phenomena such as kinetic control of equilibrium, coherency effects, impurity effects, and thermodynamic and crystallographic characteristics. The journal updates systems previously published in the Bulletin of Alloy Phase Diagrams as new data are discovered.