Crystallization of magnetic particles in nNa2O-9SrO-6Fe2O3-8B2O3 (n = 1 and 4) glasses

•Crystallization of magnetic particles from Na2O-SrO-Fe2O3-B2O3 glasses is studied.•Increase of sodium oxide content leads to decrease of crystallization temperatures.•Crystallization of 4 nm maghemite nanoparticles is observed at low temperatures.•Hexaferrite morphology and properties are determine...

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Veröffentlicht in:Journal of magnetism and magnetic materials 2019-04, Vol.476, p.311-316
Hauptverfasser: Trusov, L.A., Babarkina, O.V., Anokhin, E.O., Sleptsova, A.E., Gorbachev, E.A., Eliseev, A.A., Filippova, T.V., Vasiliev, A.V., Kazin, P.E.
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Sprache:eng
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Zusammenfassung:•Crystallization of magnetic particles from Na2O-SrO-Fe2O3-B2O3 glasses is studied.•Increase of sodium oxide content leads to decrease of crystallization temperatures.•Crystallization of 4 nm maghemite nanoparticles is observed at low temperatures.•Hexaferrite morphology and properties are determined by annealing temperatures. Magnetic glass-ceramics with composition nNa2O-9SrO-6Fe2O3-8B2O3 (n = 1 and 4) were prepared by fast quenching of the molten oxide mixtures and subsequent thermal treatment of the obtained glasses at 450–950 °C. The samples were investigated by differential thermal analysis, x-ray powder diffraction, electron microscopy, and SQIUD magnetometry. Increasing of the sodium oxide content leads to a significant decrease of the glass transition, devitrification, and melting temperatures. Just above the glass transition temperature (525 °C for n = 1 and 430 °C for n = 4) superparamagnetic γ-Fe2O3 nanoparticles precipitate, which, at elevating annealing temperature, are substituted by thin hexaferrite nanoplatelets with coercivities of 2000–4000 Oe; the annealing at higher temperatures results in crystallization of the submicron hexaferrite particles with a coercivity of up to 6000 Oe. Thus the glass-ceramics are highly applicable sources of non-sintered nanoparticles with various morphologies and magnetic properties.
ISSN:0304-8853
1873-4766
DOI:10.1016/j.jmmm.2018.12.083