论文标题
粘性液体中超顺磁性纳米颗粒组装的特性
Properties of Assembly of Superparamagnetic Nanoparticles in Viscous Liquid
论文作者
论文摘要
根据颗粒直径,交替的(AC)磁场振幅和液体粘度,对氧化铁纳米颗粒的稀释率(SAR)进行了详细计算。对于中等和中等的AC磁场,相对于颗粒各向异性场H0振幅HK hk组件的SAR粒径的函数通过粒径的函数通过特征最大值,然后达到高原,而对于足够大的大振幅,H0〜HK,H0〜HK,SAR会单调地增加粒径的功能。这种差异是实现粒子单位磁化矢量粘性和磁振荡模式的结果,以及中等和足够大的H0值的主管。发现组件的SAR仅在粘度模式下,对足够大直径的纳米颗粒成反比。在开发的磁模式下,组件的SAR实际上与粘度无关,因为在这种情况下,纳米颗粒主管仅在AC磁场方向上弱振荡。在AC磁场的中等幅度下,发现液体和实心基质中的组件的SAR值接近,除了大颗粒直径和足够低粘度的范围。然而,在大场幅度幅度幅度固体基质中纳米颗粒的随机定向组件的SAR大约是液体中的两倍,因为在固体基质中,大量的组件纳米颗粒的大部分并不是与AC磁场方向相对于AC磁场方向的最佳方向。通过与数值模拟数据进行比较,已经阐明了线性响应理论的有效性条件。
Detailed calculations of the specific absorption rate (SAR) of a dilute assembly of iron oxide nanoparticles with effective uniaxial anisotropy dispersed in a liquid are performed depending on the particle diameters, the alternating (ac) magnetic field amplitude and the liquid viscosity. For small and moderate ac magnetic field amplitudes H0 with respect to particle anisotropy field Hk the SAR of the assembly as a function of the particle diameter passes through a characteristic maximum and then reaches a plateau, whereas for sufficiently large amplitudes, H0 ~ Hk, the SAR increases monotonically as a function of particle diameter. This difference is a consequence of realization of viscous and magnetic oscillation modes for particle unit magnetization vector and director for moderate and sufficiently large H0 values, respectively. It is found that the SAR of the assembly changes inversely with the viscosity only in a viscous mode, for nanoparticles of sufficiently large diameters. In the developed magnetic mode the SAR of the assembly is practically independent of the viscosity, since in this case the nanoparticle director only weakly oscillates around the ac magnetic field direction. At moderate amplitudes of the ac magnetic field the SAR values of the assembly in the liquid and in the solid matrix are found to be close, except of the range of large particle diameters and sufficiently low viscosity. However, at large field amplitudes the SAR of randomly oriented assembly of nanoparticles in a solid matrix is approximately two times less than that in a liquid, because a significant fraction of nanoparticles of the assembly in the solid matrix is not optimally oriented with respect to the ac magnetic field direction. The conditions for the validity of the linear response theory have been clarified by comparison with the numerical simulation data.