核/壳结构磁性Fe3O4@SiO2纳米粒子的制备及表征

闵洁, 何丽华, 郑荣, 苏红莹, 支云飞, 陕绍云

现代化工 ›› 2021, Vol. 41 ›› Issue (2) : 146 -150.

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现代化工 ›› 2021, Vol. 41 ›› Issue (2) : 146-150. DOI: 10.16606/j.cnki.issn0253-4320.2021.02.028
科研与开发

核/壳结构磁性Fe3O4@SiO2纳米粒子的制备及表征

    闵洁, 何丽华, 郑荣, 苏红莹, 支云飞, 陕绍云
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Preparation and characterizations of core-shell structural Fe3O4@SiO2 magnetic nanoparticles

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摘要

在Triton X-100/正己醇/环己烷/水反相微乳液体系中,分别采用一步法和两步法制备具有核/壳结构的磁性Fe3O4@SiO2复合纳米粒子。考察了搅拌方式和超声条件对一步法产物结构、形貌的影响,并与两步法进行了对比研究。通过XRD、FT-IR、DLS、TEM和VSM对复合颗粒进行了表征。结果表明,反相微乳液体系下,一步法获得的纳米粒子团聚严重、无明显的核/壳结构,且搅拌方式和超声因素对产物微观结构影响较小;而采用两步法可以获得形貌规整的核/壳结构Fe3O4@SiO2复合纳米粒子,其室温下的磁滞回线呈超顺磁性,饱和磁化强度为37.8 emu/g。

Abstract

Core-shell structural Fe3O4@SiO2 magnetic composite nanoparticles are prepared in Triton X-100/hexanol/cyclohexane/water based inverse microemulsion system by means of one-step method and two-step method,respectively.Effects of stirring mode and ultrasonic condition on the structure and morphology of the products by one-step method are investigated and compared with that by two-step method.The resulted nanoparticles are characterized by X-ray diffraction (XRD),Fourier-infrared spectroscopy (FT-IR),dynamic laser light scattering (DLS),transmission electron microscopy (TEM) and vibrating sample magnetometer (VSM).Results indicate that nanoparticles obtained by one-step method aggregate strongly and have no obvious core/shell structure,and stirring mode and ultrasonication have little influence on the microstructure of the products.Moreover,regular core-shell structural Fe3O4@SiO2 nanoparticles can be obtained by two-step method,and the hysteresis loop at room temperature show a superparamagnetic behavior with saturation magnetization of 37.8 emu·g-1.

关键词

复合材料 / 两步法 / 一步法 / 核/壳结构 / 反相微乳液 / 纳米粒子 / 二氧化硅

Key words

composites / two-step method / one-step method / core-shell structure / inverse microemulsion / nanoparticles / SiO2

Author summay

闵洁(1995-),女,硕士研究生,研究方向为纳米材料,1342731625@qq.com

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核/壳结构磁性Fe3O4@SiO2纳米粒子的制备及表征[J]. 现代化工, 2021, 41(2): 146-150 DOI:10.16606/j.cnki.issn0253-4320.2021.02.028

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