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Investigation of the metastable spinodally decomposed magnetic CrFe-rich phase in Al doped CrFeCoNi alloy
KTH, School of Industrial Engineering and Management (ITM), Materials Science and Engineering.
China Univ Geosci, Fac Mat Sci & Chem, Wuhan 430074, Peoples R China.;Uppsala Univ, Dept Phys & Astron, Div Mat Theory, SE-75120 Uppsala, Sweden..
Chongqing Univ, Coll Mat Sci & Engn, Natl Engn Res Ctr Magnesium Alloys, Chongqing 400044, Peoples R China.;Chongqing Inst Adv Light Met, Chongqing 400030, Peoples R China..
KTH, School of Industrial Engineering and Management (ITM), Materials Science and Engineering.ORCID iD: 0000-0001-9317-6205
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2023 (English)In: Journal of Alloys and Compounds, ISSN 0925-8388, E-ISSN 1873-4669, Vol. 939, p. 168794-, article id 168794Article in journal (Refereed) Published
Abstract [en]

We have conducted an in-depth study of the magnetic phase due to a spinodal decomposition of the BCC phase of a CrFe-rich composition. This magnetic phase is present after casting (arc melting) or water quenching after annealing at 1250 degrees C for 24 h but is entirely absent after annealing in the interval 900-1100 degrees C for 24 h. Its formation is favored in the temperature interval ca 450-550 degrees C and loses magnetization above 640 degrees C. This ferromagnetic-paramagnetic transition is due to a structural transformation from ferromagnetic BCC into paramagnetic sigma and FCC phases. The conclusion from measurements at different heating rates is that both the transformation leading to the increase of the magnetization due to the spinodal decomposition of the parent phase and the vanishing magnetization at 640 degrees C are diffusion controlled.

Place, publisher, year, edition, pages
Elsevier BV , 2023. Vol. 939, p. 168794-, article id 168794
Keywords [en]
High entropy alloy, AlCrFeCoNi, Spinodal decomposition, Structural transformation, Magnetization
National Category
Metallurgy and Metallic Materials
Identifiers
URN: urn:nbn:se:kth:diva-329905DOI: 10.1016/j.jallcom.2023.168794ISI: 000996492500001Scopus ID: 2-s2.0-85146081676OAI: oai:DiVA.org:kth-329905DiVA, id: diva2:1774595
Note

QC 20230626

Available from: 2023-06-26 Created: 2023-06-26 Last updated: 2023-06-26Bibliographically approved

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Dastanpour Hosseinabadi, EsmatSchönecker, StephanStröm, ValterVitos, Levente

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