Silane treatment of Fe3O4 and its effect on the magnetic and wear properties of Fe3O4/epoxy nanocomposites

In this study, the effect of silane treatment of Fe₃O₄ on the magnetic and wear properties of Fe₃O₄/epoxy nanocomposites was investigated. Fe₃O₄ nanopowders were prepared by coprecipitation of iron(II) chloride tetrahydrate with iron(III) chloride hexahydrate, and the surfaces of Fe₃O₄ were modified with 3-aminopropyltriethoxysilane. The magnetic properties of the powders were measured on unmodified and surface-modified Fe₃O₄/epoxy nanocomposites using SQUID magnetometer. Wear tests were performed on unmodified and surface-modified Fe₃O₄/epoxy nanocomposites under the same conditions (sliding speed: 0.18 m/s, load: 20 N).The results showed that the saturation magnetization (M_s) of surface-modified Fe₃O₄/epoxy nanocomposites was approximately 110% greater than that of unmodified Fe₃O₄/epoxy nanocomposites. This showed that the specific wear rate of surface-modified Fe₃O₄/epoxy nanocomposites was lower than that of unmodified Fe₃O₄/epoxy nanocomposites. The decrease in wear rate and the increase in magnetic properties of surface-modified Fe₃O₄/epoxy nanocomposites occurred due to the improved dispersion of Fe₃O₄ into the epoxy matrix.     

Microwave synthesis of magnetic Fe3O4 nanoparticles used as a precursor of nanocomposites and ferrofluids

Methods to synthesize magnetic Fe₃O₄ nanoparticles and to modify the surface of particles are presented in the present investigation. Fe₃O₄ magnetic nanoparticles were prepared by the co-precipitation of Fe³⁺ and Fe²⁺, NH₃·H₂O was used as the precipitating agent to adjust the pH value, and the aging of Fe₃O₄ magnetic nanoparticles was accelerated by microwave (MW) irradiation. The obtained Fe₃O₄ magnetic nanoparticles were characterized by Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), X-ray powder diffraction (XRD) and vibrating sample magnetometer (VSM). The average size of Fe₃O₄ crystallites was found to be around 8–9 nm. Thereafter, the surface of Fe₃O₄ magnetic nanoparticles was modified by stearic acid. The resultant sample was characterized by FT-IR, scanning electron microscopy (SEM), XRD, lipophilic degree (LD) and sedimentation test. The FT-IR results indicated that a covalent bond was formed by chemical reaction between the hydroxyl groups on the surface of Fe₃O₄ nanoparticles and carboxyl groups of stearic acid, which changed the polarity of Fe₃O₄ nanoparticles. The dispersion of Fe₃O₄ in organic solvent was greatly improved. Effects of reaction time, reaction temperature and concentration of stearic acid on particle surface modification were investigated. In addition, Fe₃O₄/polystyrene (PS) nanocomposite was synthesized by adding surface modified Fe₃O₄ magnetic nanoparticles into styrene monomer, followed by the radical polymerization. The obtained nanocomposite was tested by thermogravimetry (TG), differential scanning calorimetry (DSC) and XRD. Results revealed that the thermal stability of PS was not significantly changed after adding Fe₃O₄ nanoparticles. The Fe₃O₄ magnetic fluid was characterized using UV–vis spectrophotometer, Gouy magnetic balance and laser particle-size analyzer. The testing results showed that the magnetic fluid had excellent stability, and had susceptibility of 4.46×10⁻⁸ and saturated magnetization of 6.56 emu/g. In addition, the mean size d (0.99) of magnetic Fe₃O₄ nanoparticles in the fluid was 36.19 nm.     

Synthesis and magnetic properties of hard magnetic (CoFe2O4)-soft magnetic (Fe3O4) nano-composite ceramics by SPS technology

CoFe₂O₄/Fe₃O₄ nano-composite ceramics were synthesized by Spark Plasma Sintering. The X-ray diffraction patterns show that all samples are composed of CoFe₂O₄ and Fe₃O₄ phases when the sintering temperature is below 900 °C. It is found that the magnetic properties strongly depend on the sintering temperature. The two-step hysteresis loops for samples sintered below 500 °C are observed, but when sintering temperature reaches 500 °C, the step disappears, which indicates that the CoFe₂O₄ and Fe₃O₄ are well exchange coupled. As the sintering temperature increases from 500 to 800 °C, the results of X-ray diffractometer indicate the constriction of crystalline regions due to the ion diffusion at the interfaces of CoFe₂O₄/Fe₃O₄ phases, which have great impact on the magnetic properties.     

海藻酸改性的空心Fe3O4纳米颗粒的制备与应用

不使用任何模板一步制得空心Fe₃O₄纳米颗粒,然后将海藻酸钠嫁接在氨基化的空心Fe₃O₄表面,再利用海藻酸盐与钙离子的作用,在空心Fe₃O₄表面形成一个凝胶化层,制得海藻酸盐凝胶化的空心Fe₃O₄纳米颗粒,粒径约为400～500 nm．采用TEM、XRD、XPS、VSM等手段对纳米微球进行表征．VSM表征结果表明在室温下样品磁性材料为超顺磁性．改性Fe₃O₄纳米颗粒成功地用于柔红霉素的载负和缓释,最大载负率和载药量分别为28.4%和14.2%．缓释结果表明,海藻酸盐凝胶化层的存在,能更有效控制柔红霉素缓慢地释放．     

Biosynthesis and magnetic properties of mesoporous Fe3O4 composites

Magnetic Fe₃O₄ materials with mesoporous structure are synthesized by co-precipitation method using yeast cells as a template. The X-ray diffraction (XRD) pattern indicates that the as-synthesized mesoporous hybrid Fe₃O₄ is well crystallized. The Barrett-Joyner-Halenda (BJH) models reveal the existence of mesostructure in the dried sample which has a specific surface area of 96.31 m²/g and a pore size distribution of 8-14 nm. Transmission electron microscopy (TEM) measurements confirm the wormhole-like structure of the resulting samples. The composition and chemical bonds of the Fe₃O₄/cells composites are studied by Fourier transform infrared (FT-IR) spectroscopy. Preliminary magnetic properties of the mesoporous hybrid Fe₃O₄ are characterized by a vibrating sample magnetometer (VSM). The magnetic Fe₃O₄/cells composites with mesoporous structure have potential applications in biomedical areas, such as drug delivery.     

Preparation and characterization of visible light responsive Fe2O3-TiO2 composites

In this study we present the effects of iron oxide (Fe₂O₃) on titanium dioxide (TiO₂) in synthesising visible-light reactive photocatalysts. A Fe₂O₃-TiO₂ composite photocatalyst was synthesized from Fe₂(SO₄)₃ and Ti(SO₄)₂ by a ethanol-assisted hydrothermal method. The preparation conditions were optimized through the investigation of the effects of hydrothermal temperature and time as well as molar ratio of Ti to Fe on the photocatalytic activity. The visual, physical and chemical properties of the Fe₂O₃-TiO₂ composites were investigated. The results showed that α-Fe₂O₃ and anatase TiO₂ were present in the composites. The Fe₂O₃-TiO₂ synthesized under optimum condition consisted of mesoporous structure with an average pore size of 4 nm and a surface area of 43 m²/g. Under visible and solar light irradiation, the photocatalytic activity of optimized sample was significantly higher than that of pure TiO₂. This sample led to a photodegradation efficiency of 90% and 40% of auramine under visible light and solar light, respectively.     

Fabrication, characterization and measurement of thermal conductivity of Fe3O4 nanofluids

Magnetite Fe₃O₄ nanoparticles were synthesized by a co-precipitation method at different pH values. The products were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, and transmission electronic microscopy. Their magnetic properties were evaluated on a vibrating sample magnetometer. The results show that the shape of the particles is cubic and they are superparamagnetic at room temperature. Magnetic nanofluids were prepared by dispersing the Fe₃O₄ nanoparticles in water as a base fluid in the presence of tetramethyl ammonium hydroxide as a dispersant. The thermal conductivity of the nanofluids was measured as a function of volume fraction and temperature. The results show that the thermal conductivity ratio of the nanofluids increases with increase in temperature and volume fraction. The highest enhancement of thermal conductivity was 11.5% in the nanofluid of 3 vol% of nanoparticles at 40 °C. The experimental results were also compared with the theoretical models.     

硅纳米孔柱阵列及其四氧化三铁复合薄膜的湿敏电容特性研究

报道了硅纳米孔柱阵列（Si-NPA），Fe₃O₄复合的Si-NPA（Fe ₃O₄/Si-NPA）两种薄 膜材料的制备方法并对其形貌和结构进行了表征，研究了其电容湿度传感特性.结果表明，S i-NPA，Fe₃O₄/Si-NPA均为微米/纳米结构复合体系.当环境相对湿 度从11％上升到95％ 时，采用100 Hz的信号频率进行测试，以Si-NPA和Fe₃O₄/Si-NPA 为电介质材料制成的湿 敏元件的电容增加值分别为起始值的1500％和5500％；采用1000 Hz的信号频率测试时，则 分别为起始值的800％和12000％，显示出两种材料较高的湿度灵敏性和较强的绝对电容输出 信号强度.同时，在升湿和降湿过程中，Si-NPA，Fe₃O₄/Si-NPA都 具有较快的响应速度 ，其响应时间分别为15 s，5 s和20 s，15 s.文章结合材料的形貌和结构特性对其物理机理 进行了分析.上述结果表明，Si-NPA无论是直接作为湿度薄膜传感材料还是作为复合薄膜湿 度传感材料的衬底都具有很好的前景. 关键词： 硅纳米孔柱阵列 3O₄')" href="#">Fe₃O₄ 湿度电容传感特性     

Nanowires of iron oxides embedded in SiO2 templates

To attain the complete filling of the channels of MCM-41 with magnetite and maghemite, we have tried out an alternative method to the incipient wetness impregnation. The mesoporous material was instilled with a Fe-carrying organic salt after subjecting the matrix to a silylation treatment. Thus, a solid of 7.7 wt.% iron-loaded MCM-41 was obtained. Different subsequent thermal treatments were used to produce γ-Fe₂O₃ or Fe₃O₄. The Mössbauer and magnetic results show that after this method, the as-prepared composite displays a size-distribution of magnetic particles. It is mainly made up of fine particles that display a superparamagnetic relaxation at room temperature and get blocked at ≈42 K for the AC susceptibility time-scale measurements both for γ-Fe₂O₃ and Fe₃O₄ particles. For both samples, about 24% of larger iron-containing phases are magnetically blocked at room temperature. For the Fe₃O₄ particles, this fraction undergoes the Verwey transition at about 110 K; in addition, there is a minor Fe (III) fraction that remains paramagnetic down to 4.2 K.     

Electromagnetic and mechanical properties of Fe3O4-coated amorphous carbon nanotube/polyvinyl chloride composites

Electromagnetic wave absorbing properties of absorbing composites depend on the dielectric and magnetic loss generally. In this paper, using Fe₃O₄-coated amorphous carbon nanotubes (ACNTs-Fe₃O₄) fabricated using a chemical synthesis–hydrothermal treatment method as an absorber and polyvinyl chloride (PVC) as a matrix, electromagnetic and mechanical properties of ACNT-Fe₃O₄/PVC composite were investigated. The results showed that the dielectric and magnetic losses of ACNT-Fe₃O₄/PVC composite were significantly enhanced in 8.2–12.4 GHz compared to ACNT/PVC composite, which improved absorbing properties, while slightly changing the mechanical properties.     

Positive and negative magnetoresistance in Fe3O4-based heterostructures

Fe₃O₄-based heterostructures, including Fe₃O₄/MgO/Fe₃O₄, Fe₃O₄/MgO/Si and Fe₃O₄/SiO₂/Si, were fabricated by magnetron sputtering to investigate the perpendicular-to-plane magneto-transport properties. In the Fe₃O₄/MgO/Fe₃O₄ and Fe₃O₄/MgO/Si heterostructures, the typical magneto-transport properties of single Fe₃O₄ films, such as negative magnetoresistance (MR) and extreme values of MR−T curves at 120 K, were observed, suggesting that the spin polarization of conducting electrons conserves through MgO barrier. MR in the Fe₃O₄/MgO/Fe₃O₄ heterostructure is larger than that in the Fe₃O₄/MgO/Si heterostructure, because the spin of electrons is disturbed in the depletion layer of Si and the SiO₂ layer introduced by Fe₃O₄/MgO growth. The Fe₃O₄/SiO₂/Si heterostructure has a positive MR of 2% at 120 K, which may originate from the scattering of conducting electrons in amorphous SiO₂ and the spin polarization reversal at the Fe₃O₄/SiO₂ interface.     

Green synthesis and characterization of superparamagnetic Fe3O4 nanoparticles

In this paper, we have first demonstrated a facile and green synthetic approach for preparing superparamagnetic Fe₃O₄ nanoparticles using α-d-glucose as the reducing agent and gluconic acid (the oxidative product of glucose) as stabilizer and dispersant. The X-ray powder diffraction (XRD), X-ray photoelectron spectrometry (XPS), and selected area electron diffraction (SAED) results showed that the inverse spinel structure pure phase polycrystalline Fe₃O₄ was obtained. The scanning electron microscopy (SEM) and transmission electron microscopy (TEM) results exhibited that Fe₃O₄ nanoparticles were roughly spherical shape and its average size was about 12.5 nm. The high-resolution TEM (HRTEM) result proved that the nanoparticles were structurally uniform with a lattice fringe spacing about 0.25 nm, which corresponded well with the values of 0.253 nm of the (3 1 1) lattice plane of the inverse spinel Fe₃O₄ obtained from the JCPDS database. The superconducting quantum interference device (SQUID) results revealed that the blocking temperature (T_b) was 190 K, and that the magnetic hysteresis loop at 300 K showed a saturation magnetization of 60.5 emu/g, and the absence of coercivity and remanence indicated that the as-synthesized Fe₃O₄ nanoparticles had superparamagnetic properties. Fourier transform infrared spectroscopy (FT-IR) spectrum displayed that the characteristic band of Fe-O at 569 cm⁻¹ was indicative of Fe₃O₄. This method might provide a new, mild, green, and economical concept for the synthesis of other nanomaterials.     

Preparation and magnetic properties of BaFe12O19/Ni0.8Zn0.2Fe2O4 nanocomposite ferrite

Nanocomposite of hard (BaFe₁₂O₁₉)/soft ferrite (Ni_0.8Zn_0.2Fe₂O₄) have been prepared by the sol–gel process. The nanocomposite ferrite are formed when the calcining temperature is above 800 °C. It is found that the magnetic properties strongly depend on the presintering treatment and calcining temperature. The “bee waist” type hysteresis loops for samples disappear when the presintering temperature is 400 °C and the calcination temperature reaches 1100 °C owing to the exchange-coupling interaction. The remanence of BaFe₁₂O₁₉/Ni_0.8Zn_0.2Fe₂O₄ nanocomposite ferrite with the mass ratio of 5:1 is higher than a single phase ferrite. The specific saturation magnetization, remanence magnetization and coercivity are 63 emu/g, 36 emu/g and 2750 G, respectively. The exchange-coupling interaction in the BaFe₁₂O₁₉/Ni_0.8Zn_0.2Fe₂O₄ nanocomposite ferrite is discussed.     

Study on dielectric and magnetic properties of Ho3Fe5O12 ceramics

Ho₃Fe₅O₁₂ ceramics with garnet structure were prepared by the solid-state reaction method. The results revealed the existence of Fe²⁺ ions have intensive influence on dielectric and magnetic properties of Ho₃Fe₅O₁₂ ceramics, which could be further confirmed by oxygen treatment. With a magnetic field lower than 10 kOe, the ME coefficient reaches 33 ps m⁻¹ at room temperature. And the ME coupling was further verified by dielectric anomaly near Néel temperature.     

Magnetic properties of Nd0.9Dy0.1Fe3(BO3)4

The magnetic properties of trigonal Nd_0.9Dy_0.1Fe₃(BO₃)₄ substituted compound with the competitive Nd-Fe and Dy-Fe exchange interactions have been investigated. It has been shown that in Nd_0.9Dy_0.1Fe₃(BO₃)₄ a spontaneous spin-reorientation transition from an ease-axis state to an easy-plane occurs near 8 K. Anomalies of the magnetization curves are observed in a spin-flop transition induced by the magnetic field B‖c. The calculations were performed using a molecular-field approximation and a crystal-field model for the rare-earth subsystem. Extensive experimental data on the magnetic properties of Nd_0.9Dy_0.1Fe₃(BO₃)₄ have been interpreted and good agreement between theory and experiment has been achieved using the obtained theoretical dependences.     

Preparation of photocatalytic Fe2O3-TiO2 coatings in one step by metal organic chemical vapor deposition

There are two major difficulties in the TiO₂ liquid-solid photocatalytic system: effective immobilization of the TiO₂ particles; and improving the catalytic activity under visible light. To simultaneously solve these two problems, Fe₂O₃-TiO₂ coatings supported on activated carbon fiber (ACF), have been prepared in one step by a convenient and efficient method—metal organic chemical vapor deposition (MOCVD). XRD results revealed that Fe₂O₃-TiO₂ coatings mainly composed of anatase TiO₂, α-Fe₂O₃ phases and little Fe₂Ti₃O₉. The pore structure of ACF was preserved well after loading with Fe₂O₃-TiO₂ coatings. UV-vis diffuse reflectance spectra showed a slight shift to longer wavelengths and an enhancement of the absorption in the visible region for Fe₂O₃-TiO₂ coatings, compared to the pure TiO₂ sample. A moderate Fe₂O₃-TiO₂ loading (13.7 wt%) was beneficial to mineralizing wastewater because the intermediates could be adsorbed onto the surface of photocatalyst following decomposition. The stable performance revealed that the Fe₂O₃-TiO₂ coatings were strongly adhered to the ACF surface, and the as prepared catalysts could be reused showing potential application for wastewater treatment.     

High heat generation ability in AC magnetic field for nano-sized magnetic Y3Fe5O12 powder prepared by bead milling

Nano-sized magnetic Y₃Fe₅O₁₂ ferrite having a high heat generation ability in an AC magnetic field was prepared by bead milling. A commercial powder sample (non-milled sample) of ca. 2.9 μm in particle size did not show any temperature enhancement in the AC magnetic field. The heat generation ability in the AC magnetic field improved with a decrease in the average crystallite size for the bead-milled Y₃Fe₅O₁₂ ferrites. The highest heat ability in the AC magnetic field was for the fine Y₃Fe₅O₁₂ powder with a 15-nm crystallite size (the samples were milled for 4 h using 0.1 mm? beads). The heat generation ability of the excessively milled Y₃Fe₅O₁₂ samples decreased. The main reason for the high heat generation property of the milled samples was ascribed to an increase in the Néel relaxation of the superparamagnetic material. The heat generation ability was not influenced by the concentration of the ferrite powder. For the samples milled for 4 h using 0.1 mm? beads, the heat generation ability (W g⁻¹) was estimated using a 3.58×10⁻⁴ fH² frequency (f/kHz) and the magnetic field (H/kA m⁻¹), which is the highest reported value of superparamagnetic materials.     

Strongly interacting superspins in Fe3O4 nanoparticles

In this paper we report structural and magnetic properties of Fe₃O₄ nanoparticles synthesized by thermal decomposition of ball milled iron nitrate and citric acid in N₂ and air ambient. The XRD pattern of samples which are prepared in air shows some impurity phases, while the samples synthesized in the N₂ atmosphere are almost pure Fe₃O₄ phase. The result shows that by increasing the particle size, the magnetization of the samples increases. The increase of magnetization by increasing the particle size could be attributed to the lower surface spin canting and surface spin disorder of the larger magnetic nanoparticles. The results of ac magnetic susceptibility measurements show that the susceptibility data are not in accordance with the Néel -Brown model for superparamagnetic relaxation, but fit well with conventional critical slowing down model which indicates that the dipole-dipole interactions are strong enough to cause superspin-glass like phase in these samples.     

Chemical quenching of positronium in Fe2O3/Al2O3 catalysts

Fe₂O₃/Al₂O₃ catalysts were prepared by solid state reaction method using α-Fe₂O₃ and γ-Al₂O₃ nano powders. The microstructure and surface properties of the catalyst were studied using positron lifetime and coincidence Doppler broadening annihilation radiation measurements. The positron lifetime spectrum shows four components. The two long lifetimes τ₃ and τ₄ are attributed to positronium annihilation in two types of pores distributed inside Al₂O₃ grain and between the grains, respectively. With increasing Fe₂O₃ content from 3 wt% to 40 wt%, the lifetime τ₃ keeps nearly unchanged, while the longest lifetime τ₄ shows decrease from 96 ns to 64 ns. Its intensity decreases drastically from 24% to less than 8%. The Doppler broadening S parameter shows also a continuous decrease. Further analysis of the Doppler broadening spectra reveals a decrease in the p-Ps intensity with increasing Fe₂O₃ content, which rules out the possibility of spin-conversion of positronium. Therefore the decrease of τ₄ is most probably due to the chemical quenching reaction of positronium with Fe ions on the surface of the large pores.     

Exchange coupling behavior in bimagnetic CoFe2O4/CoFe2 nanocomposite

In this work we report a study of the magnetic behavior of ferrimagnetic oxide CoFe₂O₄ and ferrimagnetic oxide/ferromagnetic metal CoFe₂O₄/CoFe₂ nanocomposite. The latter compound is a good system to study hard ferrimagnet/soft ferromagnet exchange coupled. Two steps were followed to synthesize the bimagnetic CoFe₂O₄/CoFe₂ nanocomposite: (i) first, preparation of CoFe₂O₄ nanoparticles using a simple hydrothermal method, and (ii) second, reduction reaction of cobalt ferrite nanoparticles using activated charcoal in inert atmosphere and high temperature. The phase structures, particle sizes, morphology, and magnetic properties of CoFe₂O₄ nanoparticles were investigated by X-Ray diffraction (XRD), Mossbauer spectroscopy (MS), transmission electron microscopy (TEM), and vibrating sample magnetometer (VSM) with applied field up to 3.0 kOe at room temperature and 50 K. The mean diameter of CoFe₂O₄ particles is about 16 nm. Mossbauer spectra revealed two sites for Fe³⁺. One site is related to Fe in an octahedral coordination and the other one to the Fe³⁺ in a tetrahedral coordination, as expected for a spinel crystal structure of CoFe₂O₄. TEM measurements of nanocomposite showed the formation of a thin shell of CoFe₂ on the cobalt ferrite and indicate that the nanoparticles increase to about 100 nm. The magnetization of the nanocomposite showed a hysteresis loop that is characteristic of exchange coupled systems. A maximum energy product (BH)_max of 1.22 MGOe was achieved at room temperature for CoFe₂O₄/CoFe₂ nanocomposites, which is about 115% higher than the value obtained for CoFe₂O₄ precursor. The exchange coupling interaction and the enhancement of product (BH)_max in nanocomposite CoFe₂O₄/CoFe₂ are discussed.