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A Novel Approach to Enhance High Temperature Therma Stability of Superparamagnetic Fe3O4 Nanoparticles

机译:一种提高超顺磁Fe3O4纳米粒子高温热稳定性的新方法

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We report a novel approach to enhance thermal stability of magnetite nanoparticles by entrapping them in silver matrix. The oleic acid capped nanoparticles of average crystallite size similar to 10 nm were synthesized through co-precipitation, followed by hydrothermal microwave assisted capping of magnetite nanoparticles with Ag matrix in ethylene glycol solvent. At similar to 160 degrees C the oleic acid is desorbed from the magnetite nanoparticles, and silver is deposited on negatively charged magnetite seeds through electrostatic attraction. The prepared particles are characterized by X-ray diffraction, high resolution transmission electron microscopy, dynamic light scattering and UV-vis spectroscopy. The surface plasmon resonance band at 479 nm and large average hydrodynamic diameter of similar to 432 nm confirm the Ag matrix around the magnetite particles. Thermal stability of prepared particles was assessed using in situ high temperature XRD, thermo gravimetric analysis and differential scanning calorimetry and the results are compared with that of oleic acid capped particles. Magnetite nanoparticles in silver matrix showed no phase conversion up to 900 degrees C, while oleic acid capped and bare nanoparticles are phase converted to nonmagnetic alpha-Fe2O3 phase between 400-450 degrees C, under vacuum annealing. A rapid growth of Fe3O4 nanoparticles at higher temperature was observed due to faster coalescence through diffusion and higher surface free energy of magnetite as compared to silver. The saturation magnetization of oleic acid capped magnetite particles in silver matrix before and after vacuum annealing at 900 degrees C were 25.4 and 46.7 emu/g, respectively. The retention of superparamagnetic behavior in silver matrix up to 900 degrees C is interesting for high temperature applications.
机译:我们通过在银基质中诱发它们来报告一种提高磁铁矿纳米颗粒的热稳定性的新方法。通过共沉淀合成平均微晶尺寸的油酸覆盖纳米颗粒,其通过共沉淀合成,然后通过乙二醇溶剂中的Ag基质进行磁铁矿纳米颗粒的水热微波辅助封盖。在类似于160℃下,油酸从磁铁矿纳米颗粒中解吸,通过静电吸引,将银沉积在带负电的磁铁矿种子上。制备的颗粒的特征在于X射线衍射,高分辨率透射电子显微镜,动态光散射和UV-Vis光谱。表面等离子体共振带在479nm处和相对于432nm的平均水动力直径相似,确认磁铁矿颗粒周围的Ag基质。使用原位高温XRD,热重量分析和差示扫描量热法评估制备颗粒的热稳定性,并将结果与​​油酸覆盖颗粒的颗粒进行比较。银基质中的磁铁矿纳米颗粒显示出高达900℃的相转换,而油酸盖和裸纳米颗粒在真空退火的真空退火下在400-450℃之间转化为非磁性α-Fe2O3相。与银相比,由于银,由于银,因此观察到Fe3O4纳米颗粒在较高温度下观察到较高温度的磁性。在900℃下,在900℃下真空退火之前和之后的银基质中的油酸封端磁铁矿颗粒的饱和磁化分别分别为25.4和46.7Mu / g。对于高达900摄氏度的银矩阵中的超顺磁性行为的保留是有趣的高温应用。

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