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Polyethylene Glycol-Mediated Synthesis of Cubic Iron Oxide Nanoparticles with High Heating Power

机译:聚乙二醇介导的高热功率立方氧化铁纳米粒子的合成

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摘要

Iron oxide magnetic nanoparticles (IOMNPs) have been successfully synthesized by means of solvothermal reduction method employing polyethylene glycol (PEG200) as a solvent. The as-synthesized IOMNPs are poly-dispersed, highly crystalline, and exhibit a cubic shape. The size of IOMNPs is strongly dependent on the reaction time and the ration between the amount of magnetic precursor and PEG200 used in the synthesis method. At low magnetic precursor/PEG200 ratio, the cubic IOMNPs coexist with polyhedral IOMNPs. The structure and morphology of the IOMNPs were thoroughly investigated by using a wide range of techniques: TEM, XRD, XPS, FTIR, and RAMAN. XPS analysis showed that the IOMNPs comprise a crystalline magnetite core bearing on the outer surface functional groups from PEG200 and acetate. The presence of physisorbed PEG200 on the IOMNP surface is faintly detected through FT-IR spectroscopy. The surface of IOMNPs undergoes oxidation into maghemite as proven by RAMAN spectroscopy and the occurrence of satellite peaks in the Fe2p XP spectra. The magnetic studies performed on powder show that the blocking temperature (TB) of IOMNPs is around 300 K displaying a coercive field in between 160 and 170 Oe. Below the TB, the field-cooled (FC) curves turn concave and describe a plateau indicating that strong magnetic dipole-dipole interactions are manifested in between IOMNPs. The specific absorption rate (SAR) values increase with decreasing nanoparticle concentrations for the IOMNPs dispersed in water. The SAR dependence on the applied magnetic field, studied up to magnetic field amplitude of 60 kA/m, presents a sigmoid shape with saturation values up to 1700 W/g. By dispersing the IOMNPs in PEG600 (liquid) and PEG1000 (solid), it was found that the SAR values decrease by 50 or 75 %, indicating that the Brownian friction within the solvent was the main contributor to the heating power of IOMNPs.Electronic supplementary materialThe online version of this article (doi:10.1186/s11671-015-1091-0) contains supplementary material, which is available to authorized users.
机译:氧化铁磁性纳米粒子(IOMNPs)已成功地通过溶剂热还原法采用聚乙二醇(PEG200)作为溶剂合成。合成后的IOMNPs是多分散的,高度结晶的,并呈立方体形状。 IOMNPs的大小在很大程度上取决于反应时间以及合成方法中使用的磁性前驱物与PEG200之间的比例。在低磁性前体/ PEG200比率下,立方IOMNP与多面体IOMNP共存。通过使用多种技术彻底研究了IOMNP的结构和形态:TEM,XRD,XPS,FTIR和RAMAN。 XPS分析表明,IOMPNs包含一个结晶磁铁矿芯,其上带有PEG200和乙酸盐的外表面官能团。通过FT-IR光谱法难以检测到IOMNP表面上有物理吸附的PEG200。 IOMNPs的表面经过RAMAN光谱证实,并在Fe2p XP光谱中出现了卫星峰,从而氧化成磁赤铁矿。对粉末进行的磁性研究表明,IOMPN的阻滞温度(TB)在300 K附近,在160至170 Oe之间显示矫顽场。在TB以下,场冷(FC)曲线变成凹形并描述一个平台,表明IOMNP之间表现出强的磁偶极-偶极相互作用。分散在水中的IOMNP的比吸收率(SAR)值随纳米颗粒浓度的降低而增加。 SAR对所施加磁场的依赖性经过研究,直到磁场振幅达到60 kA / m时,呈现出S形,饱和度值高达1700 W / g。通过将IOMNPs分散在PEG600(液体)和PEG1000(固体)中,发现SAR值降低了50%或75%,表明溶剂中的布朗摩擦是IOMNPs加热功率的主要贡献者。材料本文的在线版本(doi:10.1186 / s11671-015-1091-0)包含补充材料,授权用户可以使用。

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