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dc.contributor.authorWei, Shaolou
dc.contributor.authorKang, Jiyun
dc.contributor.authorTasan, Cemal C.
dc.date.accessioned2022-12-05T18:26:17Z
dc.date.available2022-12-05T18:26:17Z
dc.date.issued2022-11-29
dc.identifier.urihttps://hdl.handle.net/1721.1/146759
dc.description.abstractAbstract This study concerns reverse austenitic transformation of plastic strain-induced hexagonal close-packed martensite. With the aid of in situ synchrotron X-ray diffractometry, the kinetic features of the transformation and the defect content evolution in a metastable (Fe60Mn40)85Co15 alloy are quantitatively examined using 5, 20, and 100 °C/min heating rates. It is found that the reverse austenitic transformation can be activated below 200 °C and completes within a short time scale. Through a Kissinger-style kinetic analysis, the activation energy of the reverse austenitic transformation is determined as 171.38 kJ/mol, confirming its displacive nature. Although exponential attenuation is observed in both stacking fault probability and dislocation density upon the initiation of the transformation, the resulting microstructure (single-phase face-centered cubic structure) remains highly defected, exhibiting high Vickers hardness, but still preserving somewhat strain hardenability. Atomistic mechanisms for the reverse austenitic transformation are further conceived according to the crystallographic theory of martensitic transformation. Graphical abstracten_US
dc.publisherSpringer International Publishingen_US
dc.relation.isversionofhttps://doi.org/10.1557/s43578-022-00818-5en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceSpringer International Publishingen_US
dc.titleAn in situ synchrotron X-ray study of reverse austenitic transformation in a metastable FeMnCo alloyen_US
dc.typeArticleen_US
dc.identifier.citationWei, Shaolou, Kang, Jiyun and Tasan, Cemal C. 2022. "An in situ synchrotron X-ray study of reverse austenitic transformation in a metastable FeMnCo alloy."
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineering
dc.identifier.mitlicensePUBLISHER_CC
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-12-04T04:11:57Z
dc.language.rfc3066en
dc.rights.holderThe Author(s)
dspace.embargo.termsN
dspace.date.submission2022-12-04T04:11:57Z
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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