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dc.contributor.authorLobanov, M. L.en
dc.contributor.authorYurovskikh, A. S.en
dc.contributor.authorReznik, P. L.en
dc.contributor.authorNikul’chenkov, N. N.en
dc.contributor.authorRusakov, G. M.en
dc.contributor.authorRedikul’tsev, A. A.en
dc.date.accessioned2020-09-29T09:46:01Z-
dc.date.available2020-09-29T09:46:01Z-
dc.date.issued2020-
dc.identifier.citationSolid state amorphization in a thin Fe-Si-Mg-O surface film triggered by the reduction of elements from oxides in the temperature range of the α-γ transformation / M. L. Lobanov, A. S. Yurovskikh, P. L. Reznik, N. N. Nikul’chenkov, et al. . — DOI 10.22226/2410-3535-2020-1-83-88 // Letters on Materials. — 2020. — Vol. 1. — Iss. 10. — P. 83-88.en
dc.identifier.issn2218-5046-
dc.identifier.otherhttps://lettersonmaterials.com/Upload/Journals/23539/83-88.pdfpdf
dc.identifier.other1good_DOI
dc.identifier.other279737ef-f1bf-40b6-af90-dd6a075214dcpure_uuid
dc.identifier.otherhttp://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85079877888m
dc.identifier.urihttp://elar.urfu.ru/handle/10995/90105-
dc.description.abstractThe study of the processes occurring in the surface layer of the MgO coated commercial alloy Fe-3%Si-0.5%Cu (grain oriented electrical steel) demonstrated that the amorphous phase in the form of a Fe-based solid solution is formed during continuous heating in the 95%N2 + 5%H2 atmosphere. For the purposes of this study, the following methods were used: non-ambient XRD at 20 –1060°C with heating and cooling at a rate of 0.5 dps, layer-by-layer chemical analysis performed by a glow discharge analyzer, scanning electron microscopy and energy dispersive X-ray spectroscopy. ThermoCalc software was used to calculate the potential phase equilibrium states. The amorphous phase was formed in the α → γ transformation temperature range, when the heating rates were altered in the surface layer of 1 µm initially consisted of a solid α-Fe-based solution with ~1– 2 wt.% Si with (MgFe)2 SiO4, (MgFe)O, SiO2 oxide inclusions. We suppose that (MgFe)2 SiO4 oxides are partly reduced by H2 to Mg2 Si molecular complexes, which become solid solutions in the temperature range of the metastability of the α-Fe crystal lattice with subsequent amorphization as an alternative to the α → γ transition. The amorphous state is obtained at 920 – 960°C and is retained both at subsequent heating (to 1060°C) and cooling (to 20°С), which is super-stable compared to the established metallic glasses. The composition of the amorphous phase can be described by the formula Fe89.5 Si6 Mg4 Cu0.5. © 2020, Institute for Metals Superplasticity Problems of Russian Academy of Sciences. All rights reserved.en
dc.description.sponsorshipRussian Foundation for Basic Research, RFBR: 20‑08‑00332en
dc.description.sponsorshipMinistry of Education and Science of the Russian Federation, Minobrnauka: 11.1465.2014/K.en
dc.description.sponsorshipAcknowledgements. This study was conducted using equipment provided by the Laboratory of Structural Analysis Techniques and Materials and Nanomaterials Properties of CKP Ural Federal University. The study was financially supported by Government Decree No. 211 of the Russian Federation, Contract No. 02. A03.21.0006 and within the framework of the state task issued by the Ministry of Education and Science of the Russian Federation, project No. 11.1465.2014/K. The reported study was funded by RFBR, project number 20‑08‑00332.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherInstitute for Metals Superplasticity Problems of Russian Academy of Sciencesen
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.rightscc-byother
dc.sourceLetters on Materialsen
dc.subjectMETALLIC GLASSESen
dc.subjectPHASE TRANSITIONSen
dc.subjectSOLID-STATE AMORPHISATIONen
dc.subjectX-RAY DIFFRACTIONen
dc.titleSolid state amorphization in a thin Fe-Si-Mg-O surface film triggered by the reduction of elements from oxides in the temperature range of the α-γ transformationen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.rsi42407843-
dc.identifier.doi10.22226/2410-3535-2020-1-83-88-
dc.identifier.scopus85079877888-
local.affiliationUral Federal University n. a. the first President of Russia B. N. Yeltsin, 19 Mira St., Yekaterinburg, 620002, Russian Federationen
local.affiliationM. N. Miheev Institute of Metal Physics UB RAS, 18 S. Kovalevskaya St, Yekaterinburg, 620990, Russian Federationen
local.contributor.employeeLobanov, M.L., Ural Federal University n. a. the first President of Russia B. N. Yeltsin, 19 Mira St., Yekaterinburg, 620002, Russian Federation, M. N. Miheev Institute of Metal Physics UB RAS, 18 S. Kovalevskaya St, Yekaterinburg, 620990, Russian Federationru
local.contributor.employeeYurovskikh, A.S., Ural Federal University n. a. the first President of Russia B. N. Yeltsin, 19 Mira St., Yekaterinburg, 620002, Russian Federationru
local.contributor.employeeReznik, P.L., Ural Federal University n. a. the first President of Russia B. N. Yeltsin, 19 Mira St., Yekaterinburg, 620002, Russian Federationru
local.contributor.employeeNikul’chenkov, N.N., Ural Federal University n. a. the first President of Russia B. N. Yeltsin, 19 Mira St., Yekaterinburg, 620002, Russian Federationru
local.contributor.employeeRusakov, G.M., Ural Federal University n. a. the first President of Russia B. N. Yeltsin, 19 Mira St., Yekaterinburg, 620002, Russian Federation, M. N. Miheev Institute of Metal Physics UB RAS, 18 S. Kovalevskaya St, Yekaterinburg, 620990, Russian Federationru
local.contributor.employeeRedikul’tsev, A.A., Ural Federal University n. a. the first President of Russia B. N. Yeltsin, 19 Mira St., Yekaterinburg, 620002, Russian Federationru
local.description.firstpage83-
local.description.lastpage88-
local.issue10-
local.volume1-
dc.identifier.wos000514855400015-
local.identifier.pure12250533-
local.identifier.eid2-s2.0-85079877888-
local.fund.rffi20‑08‑00332-
local.identifier.wosWOS:000514855400015-
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