铁素体钴的异相合成

E. Nikishina
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The resulting intermediate products were subjected to thermal treatment at 750 °C (synthesis 1) and at 900 °C (synthesis 2) for 10–30 h in increments of 10 h. The synthesized phases and products of their thermolysis were studied by differential thermal analysis and differential thermogravimetry (DTA–DTG), X-ray diffraction analysis (XRDA), and granulometry.Results. The hydrated iron oxide sample remained amorphous even up to the crystallization temperature of 445 °C, which corresponds to the exothermic effect on the DTA curve. Further heating led to the α-modification of iron(III) oxide of the hexagonal system (a = b = 5.037 ± 0.002 Å; c = 13.74 ± 0.01 Å), which has an average particle size of 1.1 μm. XRDA results showed that a synthesis temperature of 750 °C (synthesis 1) and a heat treatment duration of 30 h were sufficient for the formation of a single-phase cobalt ferrite (a = 8.388 ± 0.002 Å) with an average particle diameter of 1.9 μm. For synthesis 2, a higher temperature of 900 °C was used because sample weight loss (about 12.5%) was observed in the temperature range of 720–810 °C based on the DTA results, which was due to the removal of SO2 and SO3. Moreover, when synthesis temperature and duration were at 900 °C and 30 h, respectively, CoFe2O4 with a = 8.389 ± 0.002 Å was formed. The results of the granulometric analysis showed that particles of different diameters were formed. The smallest particle size (1.5 μm) of cobalt ferrite was obtained by the heterophase interaction of hydrated iron(III) oxide (Fe2O3, 84.4 wt %) with an aqueous solution of cobalt sulfate with CCo = 0.147 mol/L. Conclusions. Depending on the method used for the synthesis of cobalt ferrite, particles of different diameters are formed. 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引用次数: 1

摘要

目标。本研究旨在开发合成钴铁氧体(CoFe2O4)的新方法,作为合成CoFe2O4基功能材料的前驱体,并研究所得相的物理化学性质。采用两种方法合成CoFe2O4:(1)水合氧化铁与(II, III)氧化物异相作用;(2)水合氧化铁与(II)硫酸钴水溶液(CCo = 0.147 mol/L,固液比为1:43)异相作用。在这两种情况下,前驱体都是水合氧化铁(Fe2O3, 84.4 wt %),由氯化铁(III)与浓氨溶液(6.0-9.5 mol/L)的异相相互作用得到。所得中间产物分别在750°C(合成1)和900°C(合成2)下以10小时为增量进行10 - 30小时的热处理。采用差热分析和差热重法(DTA-DTG)、x射线衍射分析(XRDA)和粒度法对其合成相和产物进行了研究。当结晶温度达到445℃时,水合氧化铁样品仍保持无定形状态,这与DTA曲线上的放热效应相对应。进一步加热导致六方体系的氧化铁(III)发生α-改性(a = b = 5.037±0.002 Å;C = 13.74±0.01 Å),平均粒径为1.1 μm。XRDA结果表明,750℃的合成温度(合成1)和30 h的热处理时间足以形成平均粒径为1.9 μm的钴铁氧体(a = 8.388±0.002 Å)。对于合成2,使用了900℃的较高温度,因为根据DTA结果,在720-810℃的温度范围内,由于SO2和SO3的去除,样品的重量损失(约12.5%)。当合成温度和时间分别为900℃和30 h时,可制得a = 8.389±0.002 Å的CoFe2O4。粒度分析结果表明,形成了不同粒径的颗粒。水合氧化铁(Fe2O3, 84.4 wt %)与CCo = 0.147 mol/L的硫酸钴水溶液异相作用,得到最小粒径为1.5 μm的铁酸钴。结论。根据合成钴铁氧体的方法不同,形成了不同直径的颗粒。通过水合氧化铁(III)与硫酸钴(II)水溶液的异相相互作用,获得了最小粒径的铁酸钴。
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Heterophase synthesis of ferrite cobalt Elena E. Nikishina
Objectives. The study aimed to develop new methods for the synthesis of cobalt ferrite (CoFe2O4), which is a precursor for the synthesis of CoFe2O4-based functional materials, as well as to study the physicochemical properties of the obtained phases.Methods. Two methods were used for the synthesis of CoFe2O4: (1) heterophase interaction of hydrated iron oxide with cobalt(II, III) oxide and (2) heterophase interaction of hydrated iron oxide with an aqueous solution of cobalt(II) sulfate (CCo = 0.147 mol/L, solid/liquid = 1:43). In both cases, the precursor was hydrated iron oxide (Fe2O3, 84.4 wt %), which was obtained by the heterophase interaction of iron(III) chloride with a concentrated ammonia solution (6.0–9.5 mol/L). The resulting intermediate products were subjected to thermal treatment at 750 °C (synthesis 1) and at 900 °C (synthesis 2) for 10–30 h in increments of 10 h. The synthesized phases and products of their thermolysis were studied by differential thermal analysis and differential thermogravimetry (DTA–DTG), X-ray diffraction analysis (XRDA), and granulometry.Results. The hydrated iron oxide sample remained amorphous even up to the crystallization temperature of 445 °C, which corresponds to the exothermic effect on the DTA curve. Further heating led to the α-modification of iron(III) oxide of the hexagonal system (a = b = 5.037 ± 0.002 Å; c = 13.74 ± 0.01 Å), which has an average particle size of 1.1 μm. XRDA results showed that a synthesis temperature of 750 °C (synthesis 1) and a heat treatment duration of 30 h were sufficient for the formation of a single-phase cobalt ferrite (a = 8.388 ± 0.002 Å) with an average particle diameter of 1.9 μm. For synthesis 2, a higher temperature of 900 °C was used because sample weight loss (about 12.5%) was observed in the temperature range of 720–810 °C based on the DTA results, which was due to the removal of SO2 and SO3. Moreover, when synthesis temperature and duration were at 900 °C and 30 h, respectively, CoFe2O4 with a = 8.389 ± 0.002 Å was formed. The results of the granulometric analysis showed that particles of different diameters were formed. The smallest particle size (1.5 μm) of cobalt ferrite was obtained by the heterophase interaction of hydrated iron(III) oxide (Fe2O3, 84.4 wt %) with an aqueous solution of cobalt sulfate with CCo = 0.147 mol/L. Conclusions. Depending on the method used for the synthesis of cobalt ferrite, particles of different diameters are formed. The smallest particle size of cobalt ferrite was obtained from the heterophase interaction of hydrated iron(III) oxide with an aqueous solution of cobalt(II) sulfate.
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