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Formation of L1(0) Ordering in FeNi by Mechanical Alloying and Field-Assisted Heat Treatment: Synchrotron XRD Studies
[Image: see text] L1(0)-ordered FeNi, tetrataenite, found naturally in meteorites is a predilection for next-generation rare-earth free permanent magnetic materials. However, the synthesis of this phase remains unattainable in an industrially relevant time frame due to the sluggish diffusion of Fe a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10116615/ https://www.ncbi.nlm.nih.gov/pubmed/37091413 http://dx.doi.org/10.1021/acsomega.2c07869 |
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author | Mandal, Shuvam Panigrahi, Ajit Rath, Ashutosh Bönisch, Matthias Sengupta, Pradyut Debata, Mayadhar Basu, Suddhasatwa |
author_facet | Mandal, Shuvam Panigrahi, Ajit Rath, Ashutosh Bönisch, Matthias Sengupta, Pradyut Debata, Mayadhar Basu, Suddhasatwa |
author_sort | Mandal, Shuvam |
collection | PubMed |
description | [Image: see text] L1(0)-ordered FeNi, tetrataenite, found naturally in meteorites is a predilection for next-generation rare-earth free permanent magnetic materials. However, the synthesis of this phase remains unattainable in an industrially relevant time frame due to the sluggish diffusion of Fe and Ni near the order–disorder temperature (593 K) of L1(0) FeNi. The present work describes the synthesis of ordered L1(0) FeNi from elemental Fe and Ni powders by mechanical alloying up to 12 h and subsequent heat treatment at 623 K for 1000 h without a magnetic field and for 4 h in the presence of 1.5 T magnetic field. Also, to address the ambiguity of L1(0) phase identification caused by the low difference in the X-ray scattering factor of Fe and Ni, synchrotron-based X-ray diffraction is employed, which reveals that 6 h milling is sufficient to induce L1(0) FeNi formation. Further milling for 12 h is done to achieve a chemically homogeneous powder. The phase fraction of L1(0)-ordered FeNi is quantified to ∼9 wt % for 12 h milled FeNi, which increases to ∼15 wt % after heat treatment. Heat treatment of the milled powder in a magnetic field increases the long-range order parameter (S) from 0.18 to 0.30. Further, the study of magnetic properties reveals a decrease in magnetic saturation and a slight increase in coercivity with the increase in milling duration. At the same time, heat treatment in the magnetic field shows a considerable increase in coercivity. |
format | Online Article Text |
id | pubmed-10116615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-101166152023-04-21 Formation of L1(0) Ordering in FeNi by Mechanical Alloying and Field-Assisted Heat Treatment: Synchrotron XRD Studies Mandal, Shuvam Panigrahi, Ajit Rath, Ashutosh Bönisch, Matthias Sengupta, Pradyut Debata, Mayadhar Basu, Suddhasatwa ACS Omega [Image: see text] L1(0)-ordered FeNi, tetrataenite, found naturally in meteorites is a predilection for next-generation rare-earth free permanent magnetic materials. However, the synthesis of this phase remains unattainable in an industrially relevant time frame due to the sluggish diffusion of Fe and Ni near the order–disorder temperature (593 K) of L1(0) FeNi. The present work describes the synthesis of ordered L1(0) FeNi from elemental Fe and Ni powders by mechanical alloying up to 12 h and subsequent heat treatment at 623 K for 1000 h without a magnetic field and for 4 h in the presence of 1.5 T magnetic field. Also, to address the ambiguity of L1(0) phase identification caused by the low difference in the X-ray scattering factor of Fe and Ni, synchrotron-based X-ray diffraction is employed, which reveals that 6 h milling is sufficient to induce L1(0) FeNi formation. Further milling for 12 h is done to achieve a chemically homogeneous powder. The phase fraction of L1(0)-ordered FeNi is quantified to ∼9 wt % for 12 h milled FeNi, which increases to ∼15 wt % after heat treatment. Heat treatment of the milled powder in a magnetic field increases the long-range order parameter (S) from 0.18 to 0.30. Further, the study of magnetic properties reveals a decrease in magnetic saturation and a slight increase in coercivity with the increase in milling duration. At the same time, heat treatment in the magnetic field shows a considerable increase in coercivity. American Chemical Society 2023-04-10 /pmc/articles/PMC10116615/ /pubmed/37091413 http://dx.doi.org/10.1021/acsomega.2c07869 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Mandal, Shuvam Panigrahi, Ajit Rath, Ashutosh Bönisch, Matthias Sengupta, Pradyut Debata, Mayadhar Basu, Suddhasatwa Formation of L1(0) Ordering in FeNi by Mechanical Alloying and Field-Assisted Heat Treatment: Synchrotron XRD Studies |
title | Formation of L1(0) Ordering in FeNi by Mechanical
Alloying and Field-Assisted Heat Treatment: Synchrotron XRD Studies |
title_full | Formation of L1(0) Ordering in FeNi by Mechanical
Alloying and Field-Assisted Heat Treatment: Synchrotron XRD Studies |
title_fullStr | Formation of L1(0) Ordering in FeNi by Mechanical
Alloying and Field-Assisted Heat Treatment: Synchrotron XRD Studies |
title_full_unstemmed | Formation of L1(0) Ordering in FeNi by Mechanical
Alloying and Field-Assisted Heat Treatment: Synchrotron XRD Studies |
title_short | Formation of L1(0) Ordering in FeNi by Mechanical
Alloying and Field-Assisted Heat Treatment: Synchrotron XRD Studies |
title_sort | formation of l1(0) ordering in feni by mechanical
alloying and field-assisted heat treatment: synchrotron xrd studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10116615/ https://www.ncbi.nlm.nih.gov/pubmed/37091413 http://dx.doi.org/10.1021/acsomega.2c07869 |
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