磁性纳米四氧化三铁在生物医学中的应用

近年来,由于磁性纳米粒子在实际应用中发挥越来越重要的作用,有关磁性纳米粒子的应用受到科学界广泛关注,特别是生物医学领域。由于磁性纳米Fe_3O_4粒子制作简单且晶体对细胞无毒,在生物医药领域大量应用,磁性纳米Fe_3O_4粒子主要通过表面包覆成为免疫磁性微球进行使用。简述了磁性纳米Fe_3O_4粒子的制备方法,重点综述了近些年磁性纳米Fe_3O_4粒子在生物医学上的应用,包括磁共振成像技术、磁分离技术、靶向药物载体技术、肿瘤热疗技术、造影剂技术,并且阐述了磁性纳米Fe_3O_4粒子的发展前景。     

Assembly of Fe3O4 nanoparticles on SiO2 monodisperse spheres

The assembly of superparamagnetic Fe₃O₄ nanoparticles on submicroscopic SiO₂ spheres have been prepared by an in situ reaction using different molar ratios of Fe³⁺/Fe²⁺ (50–200%). It has been observed that morphology of the assembly and properties of these hybrid materials composed of SiO₂ as core and Fe₃O₄ nanoparticles as shell depend on the molar ratio of Fe³⁺/Fe²⁺.     

Polyaniline/Fe3O4 nanocomposites synthesized under the direction of cationic surfactant

Polyaniline(PANi)/Fe₃O₄ nanocomposites have been prepared via in situ chemical oxidative polymerization directed with cationic surfactant cetyltrimethylammonium bromide (CTAB). The studies show that PANi can coat Fe₃O₄ nanoparticles. CTAB can produce insoluble substance with initiator of polyreaction, and plays a very important role for the coating of Fe₃O₄ nanoparticles by PANi. Many Fe₃O₄ nanoparticles are bald without being coated by PANi when CTAB is replaced by anionic surfactant, so anionic surfactant can not play the role of CTAB.     

羧甲基纤维素-Fe3O4复合纳米磁性材料的制备及其渗透性能

采用改进的氧化沉淀法在羧甲基纤维素(CMC)溶液中制备了以磁性纳米Fe3O4为核心,外包CMC的复合磁性纳米粒子。用透射电镜、X射线衍射、红外光谱、Zeta电位和震动样品磁强计对复合粒子进行了表面形貌、结构和磁学的表征。实验结果表明,CMC-Fe3O4复合纳米粒子为反尖晶石型,平均粒径约为40 nm;CMC在Fe3O4粒子表面是化学吸附;在相同pH值下,CMC-Fe3O4的表面Zeta电位低于纯相Fe3O4;CMC-Fe3O4的饱和磁化强度为36.74 emu.g-1;CMC-Fe3O4复合粒子在土壤介质中的过滤系数约为0.03 cm-1;在10 cm土柱渗透实验中,72%的CMC-Fe3O4复合粒子悬浊液穿过了土壤介质。     

Synthesis and Magnetic Properties of Fe3O4 Nanoparticles

Magnetic Fe₃O₄ nanoparticles with size below 10 nm have been prepared by the aqueous phase coprecipitation method. The Fe₃O₄ nanoparticles show typical superparamagnetism. Comparison is made between the dispersed sample and the powder sample, and the results are discussed.     

Fe3O4 包覆聚苯乙烯磁性微球的制备及性能

为研究一种应用于磁稳定流化床反应器的新型高分子磁性微球的制备方法及性能,采用悬浮聚合法制备了Fe_3O_4纳米粒子包覆聚苯乙烯磁性微球,研究了搅拌速率、加入磁性Fe_3O_4纳米粒子的时间等因素对复合微球粒径及性能的影响,运用扫描电子显微镜(SEM)、X射线衍射(XRD)、振动样品磁强计(VSM)、热重(TGA)等测试手段,表征了磁性聚苯乙烯微球的形貌特征、结构、粒径、磁学性能及Fe_3O_4的包覆量.实验结果表明:在搅拌转速为600 r/min,80℃保温10 min加入修饰Fe_3O_4纳米粒子,制备所得的磁性聚苯乙烯微球为粒径分布均匀的球状微粒;Fe_3O_4的包覆量达到5%,最高饱和磁化强度为3.73 emu/g,具有较好的超顺磁性,可应用于磁稳定流化床反应器.     

Research on hydrophobicity of electrospun Fe3O4/PVDF nanofiber membranes under different preparation conditions

Abstract

Preparation condition can affect the structure and the properties of nanofiber membrane. In order to explore suitable conditions to prepare the Fe₃O₄/PVDF nanofiber membrane with good hydrophobicity, the hydrophobicity of Fe₃O₄/PVDF nanofiber membranes obtained by electrospinning was investigated by changing preparation conditions like weight percentage of Fe₃O₄ nanoparticles, blending quality concentration of poly (vinylidene fluoride) (PVDF) and Fe₃O₄ nanoparticles, and positive voltage. And the variations of hydrophobicity of Fe₃O₄/PVDF nanofiber membranes modified by 1H, 1H, 2H, 2H-perfluorodecyl trimethoxysilane were studied. The results show that the hydrophobicity of Fe₃O₄/PVDF nanofiber membranes has changed under different preparation conditions. The contact angles of samples increased after a modification by 1H, 1H, 2H, 2H-perfluorodecyl trimethoxysilane, which indicates that the hydrophobicity of Fe₃O₄/PVDF nanofiber membranes has been enhanced.     

Preparation and characteristics of Fe3O4 magnetic thin films plated on hollow glass spheres

The surface of hollow glass spheres was deposited with a layer of Fe₃O₄ film in the open air without using ultrasound and toxic reducing reagent NaNO₂; the magnetic films of Fe₃O₄ were characterized by XRD, SEM and EDS. The intactness of the films was remarkably affected by temperature; it is favorable for the hollow glass spheres to be encapsulated completely by the Fe₃O₄ magnetic films as plating temperature increased at pH 6.7. The films exhibited ferromagnetic behavior.     

Characteristic analysis of Fe3O4 nanoparticles modified by oleic acid and undecylenic acid

Carbonization of magnetic polymer microspheres is one of the methods for the preparation of magnetic carbon materials. Fe₃O₄ magnetic particle characteristics considerably influence the magnetic content and size distribution of magnetic polymer microspheres. The characteristics of Fe₃O₄ nanoparticles modified by oleic acid (OA) and undecylenic acid (UA) were analyzed by X-ray diffraction, Fourier transform infrared, scanning electron microscopy, dynamic laser light scattering, thermogravimetry/differential thermogravimetry, vibrating sample magnetometer, and water contact angle. Fe₃O₄ nanoparticles modified by OA and UA are nearly spherical and exhibit superparamagnetism. Fe₃O₄ particle size and saturation magnetization are slightly influenced by the OA and UA composition. OA and UA both are chemically adsorbed onto Fe₃O₄ as bidentate chelates. OA shows easier adsorption onto Fe₃O₄ than UA. OA groups have an expanded arrangement on OA@Fe₃O₄, whereas UA groups have a condensed arrangement on UA@Fe₃O₄. Particle lipophilicity decreases and particle clustering increases with decreasing OA content and increasing UA content on OA-UA@Fe₃O₄ nanoparticles.     

储存时间对SMP/Fe3O4形状回复性能的影响

首先制备了形状记忆性良好、在热场和磁场中都可响应的SMP/Fe3O4纳米复合材料,将样品在形变固定后,储存不同时间,分别在热场和磁场中考察储存时间对SMP/Fe3O4回复性能的影响。结果显示,储存时间10min及储存时间为12h的样品的形状回复率均在95%以上,存储时间对于热场和磁场中形变回复性能的影响具有类似的规律,即:形变固定后储存时间延长,其起始回复温度升高,回复诱导期增长,回复的温度区间变宽。XRD、DSC、DMA测试结果表明,随储存时间的延长,样品的结晶度增加,样品熔点和熔融温度区间发生改变,从而引起相应的SMP/Fe3O4回复性能的变化。     

Application of multi-functional chestnut shell in one-step preparing Fe3O4@C magnetic nanocomposite with high adsorption performance

Chestnut shell (CS) acts as a multi-functional material in the one-step preparation of Fe₃O₄@C nanocomposite via hydrothermal method by using Fe(NO₃)₃ as Fe source without adding any other additives. The characterized results show that under required hydrothermal conditions, a proper amount of CS can reduce a certain amount of adsorbed/enriched Fe³⁺ to Fe²⁺ to ensure the 2:1 molar ration of Fe³⁺ to Fe²⁺ and the in-situ formation of goal phase Fe₃O₄ on the surface of the CS. Meanwhile, CS is carbonized to C material similar to graphene oxide. In the preparation process of the composite of Fe₃O₄@C, CS plays multiple roles, such as promoter, reductive agent, C-source, and template, to endow a certain morphology of the nanocomposite Fe₃O₄@C. The composite material shows good magnetic separability and adsorption property for methylene blue (MB) solution. Furthermore, the adsorptive kinetic behavior of the Fe₃O₄@C is investigated. The method is simple, fast, low cost and green and really realizes the full use of wasteful resource CS.     

Fe3O4／羧甲基化壳聚糖纳米粒子的制备与表征

磁性壳聚糖纳米粒子可用于药物载体及废水处理吸附剂。以化学共沉淀法制备Fe3O4纳米粒子，壳聚糖先进行羧甲基化改性，再经碳二亚胺活化，包履在Fe3O4颗粒表面,透射电镜（TEM）表明，Fe3O4纳米粒子被CMC包履，粒径约10nm；X射线衍射（XRD）分析表明复合纳米粒子中磁性物质为Fe3O4；傅立叶红外光谱（FTIR）表明壳聚糖发生羧甲基反应；磁性测试表明，Fe3O4／CMC具有超顺磁性，饱和磁化强度25.73emu／g，且有良好的磁稳定性。     

Fe3O4 magnetic nanoparticles synthesis from tailings by ultrasonic chemical co-precipitation

The aim of this study is to develop a new method for the preparation of high-value, environmentally friendly products from tailings. Magnetic Fe₃O₄ nano-powder was synthesized by ultrasonic-assisted chemical co-precipitation utilizing high purity iron separated from iron ore tailings by acidic leaching method. Magnetite particles with 15 nm average diameter were characterized by X-ray diffraction, field-emission scanning electron microscopy and vibrating sample magnetometer. Surfactant influence on particles shape and size was investigated. Fe₃O₄ nanoparticles coated with C₁₂H₂₅OSO₃Na exhibit better dispersion and uniform size. The product consisted of ferrous ferrite (Fe3O4) nanosized cubic particles with a high level of crystallinity and exhibit super-paramagnetism based on magnetization curves lacking hysteresis.     

Structural and optical properties of spray pyrolytically prepared Fe2O3 thin films

Fe₂O₃ thin film was prepared using aqueous solution of FeCl₃ by spray pyrolysis. The substrate temperature was 450°C. The lattice parametersa andc for different concentrations were calculated from X-ray diffraction study. Hexagonal structure of the Fe₂O₃ thin film was confirmed. Band gap values of Fe₂O₃ prepared from different concentrations were determined from optical transmission data.     

Kinetics of Fe(3)O(4)-CoO/Al(2)O(3) catalytic ozonation of the herbicide 2-(2,4-dichlorophenoxy) propionic acid

The presence of Fe(3)O(4)-CoO/Al(2)O(3) can improve degradation efficiency significantly during the ozonation of the herbicide 2-(2,4-dichlorophenoxy) propionic acid (2,4-DP). The main factors affecting degradation efficiency, such as pH, the catalyst concentration and addition of the scavenger, were investigated. The kinetics of the catalytic ozonation are also discussed. The results indicate that two factors, the oxidation after adsorption of 2,4-DP and the oxidation of hydroxyl radicals (OH), lead to a great enhancement in ozonation efficiency during the catalytic ozonation of 2,4-DP in the presence of Fe(3)O(4)-CoO/Al(2)O(3), in which the oxidation of the OH plays an important role. Under controlled conditions, the apparent reaction rate constants for the degradation of 2,4-DP were determined to be 2.567 × 10(-4)s(-1) for O(3) and 1.840 × 10(-3)s(-1) for O(3)/Fe(3)O(4)-CoO/Al(2)O(3). The results from the analysis of the reaction kinetics using the relative method showed that O(3)/Fe(3)O(4)-CoO/Al(2)O(3) possessed a larger R(ct) (R(ct) is defined as the ratio of the ·OH exposure to the O(3) exposure, R(ct) = ∫C(t)(OH) dt/C(t)O(3)dt) than O(3), indicating that O(3)/Fe(3)O(4)-CoO/Al(2)O(3) produced more hydroxyl radicals.     

Microwave assisted fast fabrication of Fe3O4-MWCNTs nanocomposites and their application as MRI contrast agents

Uniform Fe₃O₄ nanoparticles with diameters of 3-5 nm are successfully decorated onto the external walls of multiwall carbon nanotubes (MWCNTs) by in situ high-temperature decomposition of Fe(acac)₃ in polyol solution under the irradiation of microwave. With this method, reaction time of forming Fe₃O₄-MWCNTs nanocomposites has been significantly shortened to 15 min. The resulting Fe₃O₄-MWCNTs nanocomposites show superparamagnetic property at room temperature and can be remained as stable aqueous dispersion for 2 months. Longitudinal relaxivity (r₁) and transverse relaxivity (r₂) of the magnetic MWCNTs are 8.34 Fe mM⁻¹ S⁻¹ and 146 Fe mM⁻¹ S⁻¹ respectively. The much higher r₂ value and the obvious change in the gray scale of MR images confer the Fe₃O₄-MWCNTs nanocomposites as potential candidates for T₂-weighted MRI contrast agents.     

Recent progress in Fe3O4 based magnetic nanoparticles: from synthesis to application

Fe₃O₄ based magnetic polymer nanoparticles (MPNPs) are densely studied for several decades. These Fe₃O₄ based MPNPs can be used in wastewater treatment and biological field such as magnetic resonance imaging contrast agents, hyperthermia therapy and protein separation. The Fe₃O₄ based MPNPs are attractive because they combine the advantages of magnetism and polymers together. In order to obtain the practical application in the above mentioned areas, the bare Fe₃O₄ needs to be functionalised with different kinds of molecules like organic small molecules and polymers and some inorganic molecules like silica, metals and carbon. In this review, the chemical preparation methods, different modification methods and various applications of the Fe₃O₄ based MPNPs are introduced.     

Preparation of Fe3O4/PVA nanofibers via combining in-situ composite with electrospinning

A novel approach, combining in-situ composite method with electrospinning, was used to prepare high magnetic Fe₃O₄/poly(vinyl alcohol) (PVA) composite nanofibers. Fe₃O₄ magnetic fluids were synthesized by chemical co-precipitation method in the presence of 6 wt.% PVA aqueous solution. PVA was used as stabilizer and polymeric matrix. The resulting Fe₃O₄/PVA composite nanofibers were characterized with field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and X-ray diffractometer (XRD), respectively. These composite fibers showed a uniform and continuous morphology, with the Fe₃O₄ nanoparticles embedded in the fibers. Magnetization test confirmed that the composite fiber showed a high saturated magnetization (M_s = 2.42 emµ·g^-1) although only 4 wt.% content.     

钴铁氧体/聚吡咯复合材料的制备及电磁性能

首先采用溶胶-凝胶法制备钴铁氧体,再使用水热原位合成钴铁氧体(CoFe₂O₄,CFO)/聚吡咯(polypyrrole,PPy)新型复合材料。采用X射线衍射仪(XRD)分析样品的相结构、扫描电子显微镜(SEM观察样品微观形貌、振动样品磁场计(VSM)测试样品磁性能表征样品磁性能、样品的电磁参数采用矢量网络分析仪分析,计算获得样品在(8～12)GHz频率范围内的反射损耗。结果表明:在以酒石酸为络合剂、pH=5左右、经650 ℃热处理,得到结晶度良好的尖晶石结构钴铁氧体,平均粒径为350 nm;原位聚合后得到的钴铁氧体/聚吡咯复合材料表现出良好的吸波性能,在涂层厚度1.5 mm,PPy含量为6%时,吸波性能最佳,在频率为8.66 GHz处达到-11.05 dB,小于-5 dB的频段范围为(7.49~11.43)GHz,其可作为一种轻质、宽频的雷达波吸收剂来使用。