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Abstract. The present study is concerned with the fabrication and characterization of Me2Y substituted hexaferrites, Ba2Me2Fe12-xTxO22 (Me = Co 2+ , Mg 2+ , and Cr 2+ , and T = Fe 3+ , and Ga 3+ ). The samples were prepared by the conventional ball milling technique and sintering at 1200° C. The effect of the choices of Me and T ions on the structural and magnetic properties of the hexaferrites were investigated. XRD patterns, magnetic parameters, and Mössbauer spectra of the Co2Y were consistent with a single phase Y-type hexaferrite. However, the CoCr-Y sample was found to be dominated by the Y-type hexaferrite, and M-type and BaCrO4 minority phases were observed in the XRD pattern of the sample. The small increase in saturation magnetization from about 34 emu/g up to 37.5 emu/g was therefore attributed to the development of the M-type phase. On the other hand,

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Molybdenum-zinc substituted hexaferrites were synthesized by high-energy ball milling and subsequent sintering at different temperatures (1100, 1200, and 1300° C). The samples sintered at 1100° C exhibited good hard magnetic properties, although a decrease in saturation magnetization from 70.2 emu/g for the unsubstituted sample down to 57 emu/g for the sample with x = 0.3 was observed. The drop in saturation magnetization results mainly from the presence of secondary nonmagnetic oxides. The samples sintered at temperatures ≥1200° C showed an improvement in saturation magnetization, and a sharp drop in coercivith. This behavior was associated with the development of the W-type hexaferrite, the particle growth, and possibly the spin reorientation transition from easy-axis to easy-plane.

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In this article we report on the structural and magnetic properties of BaFe12-4xMoxZn3xO19hexaferrites with Mo-Zn substitution for Fe ions. The starting materials were commensurate with the BaM stoichiometry, and the Mo:Zn ratio was 1:3. The powder precursors were prepared by high energy ball milling, and subsequently sintered at temperatures from 1100 to 1300° C. The structural analyses indicated that all samples sintered at 1100° C were dominated by a major M-type hexaferrite phase. The relative abundance of the BaMoO4and Zn-spinel secondary phases increased with increasing the concentration of the substituents, resulting in a decrease of the saturation magnetization from about 67 emu/g (forx= 0.0) to 55 emu/g (forx= 0.3). The coercivity also decreased from 3275 Oe (forx= 0.0) to 900 Oe (forx= 0.3), demonstrating the ability to tune the coercivity to the range useful for magnetic recording by the substitution process. The saturation magnetization improved significantly with sintering atT> 1100° C, and the coercivity decreased significantly, signaling the transformation of the samples to soft magnetic materials. These magnetic changes were due to the high-temperature reaction of the spinel phase with the BaM phase to produce the W-type hexaferrite phase on the one hand, and to the growth of the particles on the other hand. The magnetic phases were further investigated using Mössbauer spectroscopy and thermomagnetic measurements. Our study indicated that the sample withx= 0.2 has the highest saturation magnetization (74 emu/g at sintering temperature of 1300° C) and a tunable coercivity between 2100 Oe and 450 Oe.

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