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In Situ Synthesis of Silica-Coated Magnetite Nanoparticles by Reverse Coprecipitation Method

机译:逆共沉淀法原位合成二氧化硅包覆的磁铁矿纳米粒子

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摘要

Silica-coated magnetite nanoparticles were synthesized by reverse coprecipitation of Fe~(2+) and Fe~(3+) with sodium hydroxide in the presence of sodium silicate solution. Effect of reaction conditions and various amounts of sodium silicate solution on the powder particle characteristics was investigated by X-ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FT-IR), laser particle size analyzer (LPSA), streaming current potential and vibrating sample magnetometer (VSM) techniques. Also, stability of silica-coated magnetite nanoparticles in the acidic condition has been studied by titration method. FT-IR results revealed that silica chemisorbed on the surface of magnetite nanoparticles by Fe-O-Si bonds. Analysis of the XRD patterns confirmed the formation of magnetite having spinel structure in the presence of sodium silicate solution. FE-SEM micrographs revealed that the mean particle size of spherical magnetite decreased from 50 to less than 25 nm by adding sodium silicate solution. Agglomeration declined when the volume ratio of sodium silicate/sodium hydroxide was 0.1. This was attributed to the coating of magnetite nanoparticles by silica. Coating of magnetite by silica prevents the formation of hydrogen bondings between magnetite and water molecules. Further increase in the sodium silicate concentration revealed a reverse effect.
机译:在硅酸钠溶液存在下,用氢氧化钠对Fe〜(2+)和Fe〜(3+)进行共沉淀,合成了二氧化硅包覆的磁铁矿纳米粒子。通过X射线衍射(XRD),场发射扫描电子显微镜(FE-SEM),傅里叶变换红外光谱(FT-IR),激光研究了反应条件和不同量的硅酸钠溶液对粉末颗粒特性的影响。粒度分析仪(LPSA),流电势和振动样品磁力计(VSM)技术。另外,已经通过滴定法研究了二氧化硅涂覆的磁铁矿纳米颗粒在酸性条件下的稳定性。 FT-IR结果表明,二氧化硅通过Fe-O-Si键化学吸附在磁铁矿纳米颗粒的表面上。对XRD图谱的分析证实了在硅酸钠溶液存在下形成具有尖晶石结构的磁铁矿。 FE-SEM显微照片显示,通过添加硅酸钠溶液,球形磁铁矿的平均粒径从50 nm减小到小于25 nm。当硅酸钠/氢氧化钠的体积比为0.1时,附聚降低。这归因于二氧化硅对磁铁矿纳米颗粒的涂覆。二氧化硅对磁铁矿的涂层可防止磁铁矿和水分子之间形成氢键。硅酸钠浓度的进一步增加显示出相反的作用。

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