Influence of Fe2O3 on alloying and magnetic properties of Fe–Al

•The Fe–Al alloying in a presence of Fe2O3 is detected after 2h of milling.•The Fe–25at.% Al substitutional solid solution is formed.•Next milling steps yield Al decrease in the alloy and hematite dissolution.•Dynamic process is reflected by changes in magnetic properties.•Intergrain exchange coupli...

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Veröffentlicht in:Materials science & engineering. B, Solid-state materials for advanced technology Solid-state materials for advanced technology, 2014-08, Vol.186, p.73-78
Hauptverfasser: Jiraskova, Y., Bursik, J., Zivotsky, O., Cuda, J.
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Sprache:eng
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Zusammenfassung:•The Fe–Al alloying in a presence of Fe2O3 is detected after 2h of milling.•The Fe–25at.% Al substitutional solid solution is formed.•Next milling steps yield Al decrease in the alloy and hematite dissolution.•Dynamic process is reflected by changes in magnetic properties.•Intergrain exchange coupling yields dipolar interactions at low magnetic fields. The present study is devoted to changes of the magnetic properties during the high-energy ball milling of the Fe, Al and Fe2O3 powders. The magnetic properties are supported by the structure morphology, phase composition, and changes in atomic ordering investigated using the structure sensitive scanning electron microscopy, X-ray diffraction and Mössbauer spectrometry. Intergrain exchange coupling results in negative values of δM(H) Henkel graphs yielding dipolar interactions among particles and only slightly depending on the milling time. The bcc-Fe–Al is detected after 2h of milling coexisting with the α-(Fe,Al)2O3, superparamagnetic oxides, and α-Fe. In the next milling steps the changes in the phase composition are seen. While a small amount of the superparamagnetic oxides and the bcc-Fe–Al phase are detected after 20h, the α-(Fe,Al)2O3 has been dissolved. An increase in the hyperfine induction and saturation magnetization evidences a decrease in Al content in the bcc-Fe–Al estimated to be bellow 18at.% Al.
ISSN:0921-5107
1873-4944
DOI:10.1016/j.mseb.2014.03.012