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Nanocrystalline Mn-Zn-ferrite by novel oxalato-hydrazinated complex method

机译:新型草酸肼络合法制备纳米晶锰锌铁氧体

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We report here for the first time the synthesis of technologically important ferrite, using a metal oxalato-hydrazinate (MOH) complex method. The MOH complex of iron-manganese-zinc was synthesized at room temperature using the precursors, ferrous ammonium sulphate, manganese acetate and zinc acetate. Thermo-gravimetric studies of MOH intermediate showed complete phase formation of MnZnFe_2O_4 at 280 ℃. XRD data showed the formation of single phase cubic spinel MnZnFe_2O_4. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) demonstrate the spherical shape particle morphology. TEM images indicated the particle size of ferrite powder in the range of 20-36nm. Magnetization of synthesized nano-sized Mno.69Zno.19Fe2.12O4 was observed coercive force (H_c) at 127.82 Oe with a saturation magnetization (M_s), 34.5 emu g~(-1) using vibrating sample magnetometer (VSM) at room temperature. Mossbauer study of nano-sized ferrite powder showed super-paramagnteic behavior.
机译:我们在这里首次报告使用草酸肼基金属酸盐(MOH)络合物方法合成技术上重要的铁氧体。室温下使用前驱体,硫酸亚铁铵,乙酸锰和乙酸锌合成了铁-锰-锌的MOH络合物。 MOH中间体的热重分析表明,在280℃时MnZnFe_2O_4完全形成相。 XRD数据表明单相立方尖晶石MnZnFe_2O_4的形成。扫描电子显微镜(SEM)和透射电子显微镜(TEM)证明了球形颗粒的形态。 TEM图像表明铁氧体粉末的粒径在20-36nm范围内。在室温下使用振动样品磁力计(VSM)在127.82 Oe的矫顽力(H_c)下观察到矫顽力(H_c),饱和磁化强度(M_s)为34.5 emu g〜(-1)。 Mossbauer对纳米铁氧体粉末的研究显示出超顺磁行为。

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