Iron phthalocyanine oligomer/Fe3O4 hybrid microspheres and their microwave absorption property

The novel nano-scale iron phthalocyanine oligomer/Fe₃O₄ (FePc/Fe₃O₄) hybrid microspheres were synthesized from iron phthalocyanine oligomer and FeCl₃·6H₂O via a solvent-thermal crystallization route. The morphology and structure of the hybrid microspheres were characterized by Fourier transform infrared spectrophotometer, X-ray diffraction, scanning electron microscopy and transmission electron microscopy. These results showed that the hybrids were monodisperse microspheres and the morphology can be adjusted by controlling pre-polymerization time. The saturation magnetization increased with increase in the pre-polymerization time, while the coercivities decreased. The FePc/Fe₃O₄ hybrid microspheres exhibited novel microwave electromagnetic properties: the dielectric loss was enhanced when the pre-polymerization time increased and a new microwave loss peak appeared at high frequency. The microwave absorbing properties enhanced with increase in the pre-polymerization time and a maximum reflection loss of −29.7 dB was obtained at 11.7 GHz with 6 h of pre-polymerization time when the matching thickness was 3.0 mm. The novel hybrid materials are believed to have potential applications as microwave absorbing materials.     

Preparation and microwave absorption properties of Fe-phthalocyanine oligomer/Fe3O4 hybrid microspheres

The novel nano-scale Fe-phthalocyanine oligomer/Fe₃O₄ hybrid microspheres were synthesized from bis-phthalonitrile and FeCl₃·6H₂O through a simple solvent-thermal route. The morphology and structure of the hybrid microspheres were characterized by FTIR, XRD, SEM and TEM. These results showed that the hybrids were monodispersed solid microspheres and the morphology can be adjusted by controlling the addition of bis-phthalonitrile. On the basis of these results, the formation process was discussed. Magnetization measurement indicated that saturation magnetizations decreased linearly with increasing the addition of bis-phthalonitrile, while coercivities increased. The microwave absorption properties were measured by a vector network analyzer. The dielectric loss of the hybrid microspheres was larger and a new magnetic loss peak appeared at high frequency. The microwave absorbing properties enhanced with increasing the addition of bis-phthalonitrile and a maximum reflection loss of −31.1 dB was obtained at 8.6 GHz with 1 g bis-phthalonitrile when the matching thickness was 3.0 mm. The novel hybrid materials are believed to have potential applications in the microwave absorbing performances.     

Facile synthesis and electrochemical properties of hierarchical MnO2 submicrospheres and LiMn2O4 microspheres

Hierarchical MnO₂ submicrospheres have been successfully synthesized by a wet chemical method. The as-prepared products were characterized by means of XRD, SEM, FTIR, TG, and TEM. With the as-prepared MnO₂ submicrospheres as precursors, LiMn₂O₄ microspheres were conveniently prepared by a simple solid-state reaction between MnO₂ and LiOH at a temperature as low as 600 °C. Electrochemical properties of the as-prepared MnO₂ submicrospheres and LiMn₂O₄ microspheres as cathode materials in lithium ion cells were investigated by galvanostatic charge/discharge tests.     

Preparation and dual microwave-absorption properties of carboxylic poly(arylene ether nitrile)/Fe3O4 hybrid microspheres

The carboxylic poly(arylene ether nitrile)/Fe₃O₄ hybrid microspheres were prepared via solvothermal method. The carboxylic poly(arylene ether nitrile) (PEN-COOH) was introduced into the Fe₃O₄ microspheres by chemisorption with mass content up to 15% as defined by infrared spectra and thermal gravimetric analysis. The hybrid sphere is of hierarchical polymer-inorganic microstructure as observed by transmission electron microscopy. The microwave-absorption of the sample owns a shifting peak and a special immobilized peak with the variation of absorber thickness from 3 to 5 mm. Maximum microwave-absorption of the product is capable of over −30 dB in the range of 10-12 GHz. By proposed equivalent filter circuit model, the immobilized peak was attributed to the ordered nanostructure where the Fe₃O₄ nanocrystals were isolated by PEN-COOH. The product has the potential to be applied as microwave absorber with high microwave-absorption, good dispersibility and robust polymer-inorganic interfacial adherence.     

Magnetic and rheological properties of monodisperse Fe3O4 nanoparticle/organic hybrid

Fe₃O₄ nanoparticle/organic hybrids were synthesized via hydrolysis using iron (III) acetylacetonate at ∼80 °C. The synthesis of Fe₃O₄ was confirmed by X-ray diffraction, selected-area diffraction, and X-ray photoelectron spectroscopy. Fe₃O₄ nanoparticles in the organic matrix had diameters ranging from 7 to 13 nm depending on the conditions of hydrolysis. The saturation magnetization of the hybrid increased with an increase in the particle size. When the hybrid contained Fe₃O₄ particles with a size of less than 10 nm, it exhibited superparamagnetic behavior. The blocking temperature of the hybrid containing Fe₃O₄ particles with a size of 7.3 nm was 200 K, and it increased to 310 K as the particle size increased to 9.1 nm. A hybrid containing Fe₃O₄ particles of size greater than 10 nm was ferrimagnetic, and underwent Verwey transition at 130 K. Under a magnetic field, a suspension of the hybrid in silicone oil revealed the magnetorheological effect. The yield stress of the fluid was dependent on the saturation magnetization of Fe₃O₄ nanoparticles in the hybrid, the strength of the magnetic field, and the amount of the hybrid.     

Synthesis and studies of trisubstituted biphthalonitrile/Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> magnetic hybrid microspheres

New trisubstituted biphthalonitrile/magnetite (TSB/Fe₃O₄) magnetic hybrid microspheres were synthesized from TSB and FeCl₃ · 6H₂O using the method of one-stage thermal temperature crystallization of solvents. The morphology and structure of magnetic hybrid microspheres were inspected using a scanning electron microscope, IR Fourier spectroscopy, and X-ray diffraction. It was found that the grown TSB/Fe₃O₄ magnetic hybrid microspheres represent spherical particles with an average size of ~137 nm and a small size spread. The size and size distribution of magnetic hybrid microspheres can be controlled by a small change in the ratio of TSB and Fe³⁺ ion contents in the microsphere. TSB/Fe₃O₄ hybrid microspheres exhibit a rather high saturation magnetization (58.16 emu g^–1) and new microwave electromagnetic properties, i.e., lower (in comparison with published) dielectric losses at low frequencies; magnetic losses are increased obviously due to an increase in the TSB content. Furthermore, it is detected that magnetic hybrid microspheres absorb microwaves, and strong reflection losses in a wide frequency range are established. The effective reflection loss of–31 dB is obtained in the microwave range from 2 to 16 GHz due to TSB content variations. Wide absorption properties of microwaves along with regular spherical shape and excellent magnetic properties offer wide opportunities for various applications of TSB/Fe₃O₄ magnetic hybrid microspheres as functional materials.     

Fe3O4/β-CD的高压电学性质研究

 高压下的电学性质测量是获得材料物理性质的有效手段。利用集成在金刚石对顶砧上的薄膜微电路,测量了高压下Fe₃O₄/β-CD（β-糊精）的电导率,并分析了电导率随压力的变化关系。在0～39.9 GPa范围内,Fe₃O₄/β-CD的电导率随压力的增加而逐渐增大,并呈半导体的特征;而在17.0 GPa处其电导率发生突变,表明样品发生了高压相变。在卸压过程中,电导率随压力的变化呈线性关系,并且卸压后样品的电导率不能回到最初的状态,推测这是一个不可逆的高压结构相变。     

Only Ku-band microwave absorption by Fe3O4/ferrocenyl-CuPc hybrid nanospheres

A novel kind of hybrid nanospheres made of Fe₃O₄ and ferrocenyl-CuPc (FCP) was prepared via effective solvothermal method and performed microwave absorptivity only in Ku-band with minimum reflection loss of −25 dB at 16.0 GHz corresponding to absorbing about 99.7% content of microwave. Scanning electron microscopy images indicated that the nanospheres with uniform particle size distribution have the average diameter of 135 nm. Due to the synergistic reaction between magnetic ferrocenyl-CuPc and Fe₃O₄, the hybrid nanospheres showed novel electromagnetic properties. The real part of complex permittivity of hybrid nanospheres remains stable in the range of 0.5–12.0 GHz and has a large fluctuation at 16.5 GHz. Moreover, the dielectric loss of hybrid nanospheres also appeared a sharp peak at 16.3 GHz with the value of 2.7. The specific gravity of hybrid nanospheres is about 2.08. On the basis of these results, the novel hybrids are believed to have potential applications in the microwave absorbing area in Ku-band.     

Synthesis of magnetic and lightweight hollow microspheres/polyaniline/Fe3O4 composite in one-step method

After hollow microspheres (HM) were surface modified, a layer of electromagnetic polyaniline/Fe₃O₄ composite (PAN/Fe₃O₄) was successfully grafted onto the surface of the self-assembled monolayer coated HM, resulting in HM/PAN/Fe₃O₄ composites. In this approach, γ-aminopropyltriethoxy silane was adopted to form a well-coating monolayer with amino groups for the graft polymerization of aniline, which played an important role in fabricating the core-shell structure. FeCl₃ was used as the oxidant not only for aniline to form PAN, but also for FeCl₂ to prepare the magnets. The structure, morphologies, and magnetic properties of the as-prepared samples were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction and vibrating sample magnetometer. The results indicated that the HM/PAN/Fe₃O₄ composites possess low density (ρ < 1.0 g/cm³), controllable morphology, and good magnetic properties at room temperature (saturation magnetization Ms = 8.32 emu g⁻¹ and coercive force Hc ≈ 0).     

A simplified method for synthesis of Fe3O4@PAA nanoparticles and its application for the removal of basic dyes

A simplified method for synthesis of polyacrylic acid-bound iron oxide magnetic nanoparticles (Fe₃O₄@PAA NPs) was reported. The as-prepared nanoparticles were characterized by TEM, FT-IR, VSM and XRD. Characterization results indicated that PAA was successfully introduced onto the surface of Fe₃O₄ and did not cause any changes in magnetic property. The Fe₃O₄@PAA NPs were used to adsorb rhodamine 6G (R6G) as a model basic dye pollutant from aqueous solution. Kinetics data and adsorption isotherms were better fitted by pseudo-second-order kinetic model and Langmuir isotherm, respectively. The adsorption equilibrium could be reached at about 20 min, showing that the as-prepared adsorbent exhibited extremely rapid adsorption rate. The aqueous solution of the Yellow River was chosen as the test sample, and the results showed that the magnetic adsorbent was efficient for the removal of the basic dye in the real sample.     

Effects of sintering temperature on grain growth and the complex permeability of Co0.2Ni0.3Zn0.5Fe2O4 material prepared using mechanically alloyed nanoparticles

Nanoparticle-sized Co_0.2Ni_0.3Zn_0.5Fe₂O₄ was prepared using mechanical alloying and sintering. The starting raw materials were milled in air and subsequently sintered at various temperatures from 600 to 1300 °C. The effects of sintering temperature on physical, magnetic and electrical characteristics were studied. The complex permittivity and permeability were investigated in the frequency range 10 MHz to 1.0 GHz. The results show that single phase Co_0.2Ni_0.3Zn_0.5Fe₂O₄ could not be formed during milling alone and therefore requires sintering. The crystallization of the ferrite sample increases with increasing sintering temperature; which decrease the porosity and increase the density, crystallite size and the shrinkage of the material. The maximum magnetization value of 83.1 emu/g was obtained for a sample sintered at 1200 °C, while both the retentivity and the coercivity decrease with increasing the sintering temperature. The permeability values vary with both the sintering temperature and the frequency and the absolute value of the permeability decreased after the natural resonance frequency. The real part of the permittivity was constant within the measured frequency, while the loss tangent values decreased gradually with increasing frequency.     

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.     

利用天然磁铁矿简易绿色合成磁性Fe3C@C纳米材料

采用改进的溶胶凝胶法，以天然磁铁矿为铁源，开发出一种制备过程简单且环境友好且低成本的磁性Fe₃C@C纳米材料制备策略. 其中，柠檬酸作为多元羧酸络合剂，不但可以有效地溶解不同铁源，例如Fe、Fe₃O₄或天然磁铁矿，形成柠檬酸铁盐络合物；还可以在热解过程中作为碳源，形成包裹碳层. 通过控制高温热解过程可以直接形成特殊的核-壳结构形态. Fe₃C@C纳米材料具有超顺磁性特性(38.09 emu/mg).     

Magnetism and thermal induced characteristics of Fe2O3 content bioceramics

Magnetic properties of Li₂O–MnO₂–CaO–P₂O₅–SiO₂ (LMCPS) glasses doped with various amounts of Fe₂O₃ were investigated. There is a dramatic change in the magnetic property of pristine LMCPS after the addition of Fe₂O₃ and crystallized at 850 °C for 4 h. Both the electron paramagnetic resonance and magnetic susceptibility measurements showed that the glass ceramic with 4 at% Fe₂O₃ exhibited the coexistence of superparamagnetism and ferromagnetism at room temperature. When the Fe₂O₃ content was higher than 8 at%, the LMCPS glasses showed ferromagnetism behavior. The complex magnetic behavior is due to the distribution of (Li, Mn)ferrite particle sizes driven by the Fe₂O₃ content. The thermal induced hysteresis loss of the crystallized LMCPS glass ceramics was characterized under an alternating magnetic field. The energy dissipations of the crystallized LMCPS glass ceramics were determined by the concentration and Mn/Fe ratios of Li(Mn, Fe)ferrite phase formed in the glass ceramics.     

Microwave dielectric and magnetic properties of superparamagnetic 8-nm Fe3O4 nanoparticles

The superparamagnetic 8-nm Fe₃O₄ nanoparticles were successfully prepared by chemical oxidation process. For the complex permittivity, the dual dielectric relaxation processes have been proved by two overlapped Cole–Cole semicircles, and the natural resonance frequency is 3.03 GHz for the complex permeability. The maximum reflection loss value reaches −55.5 dB at 6.11 GHz with 3.85 mm in the thickness of the absorbers for the superparamagnetic 8-nm Fe₃O₄ nanoparticles which is better than that of 150 nm and 30 nm Fe₃O₄ nanoparticles. It is believed that the superparamagnetic 8-nm Fe₃O₄ nanoparticles can be used as a kind of candidate for microwave absorber.     

Synthesis and characterization of TiO2/Fe2O3 core-shell nanocomposition film and their photoelectrochemical property

TiO₂/Fe₂O₃ core-shell nanocomposition film has been fabricated via two-step method. TiO₂ nanorod arrays are synthesized by a facile hydrothermal method, and followed by Fe₂O₃ nanoparticles deposited on TiO₂ nanorod arrays through an ordinary chemical bath deposition. The phase structures, morphologies, particle size, chemical compositions of the composites have been characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FESEM) and ultraviolet-visible (UV-vis) spectrophotometer. The results confirm that Fe₂O₃ nanoparticles of mean size ca. 10 nm coated on the surface of TiO2 NRs. After depositing Fe₂O₃, UV-vis absorption property is induces the shift to the visible-light range, the annealing temperature of 600 °C is the best condition for UV-vis absorption property of TiO₂/Fe₂O₃ nanocomposite film, and increasing Fe content, optical activity are enhanced one by one. The photoelectrochemical (PEC) performances of the as-prepared composite nanorods are determined by measuring the photo-generated currents under illumination of UV-vis light. The TiO₂ NRs modified by Fe₂O₃ show the photocurrent value of 1.36 mA/cm² at 0 V vs Ag/AgCl, which is higher than those of unmodified TiO₂ NRs.     

Preparation of superparamagnetic Fe3O4/PMMA nano composites and their magnetorheological characteristics

Fe₃O₄/PMMA composite particles were fabricated by a simple one-pot hydrothermal method. The magnetic measurement showed that the composite particles displayed a higher saturated magnetization and superparamagnetic property. The rheological properties of the magnetorheological fluids (MRFs) based on Fe₃O₄/PMMA particles were measured on a rotational rheometer with a magnetic field generator. It was found that the MRFs exhibited better MR effect and sendimentary stability than the similar materials.     

Preparation of poly(styrene-glucidylmethacrylate)/Fe3O4 composite microspheres with high magnetite contents

Magnetic polymer composite microspheres with high magnetite contents were prepared by dispersion polymerization of styrene (St) and glucidylmethacrylate (GMA), in which Fe₃O₄ nanoparticles were co-stabilized by oleic acid and silane surfactants. The microstructure of the composite microspheres was characterized by Fourier transform infrared (FTIR) spectrometry, X-ray diffraction (XRD) and transmission electron microscopy (TEM). Results demonstrated the presence of a hybrid morphology with organic polymer-encapsulated inorganic particles. Subsequently, thermogravimetric analysis (TGA) and vibrating sample magnetometry (VSM) were used to evaluate the magnetite content of the microspheres. It was found that an accordant magnetite content of about 70 wt%, could be obtained for the magnetic polymer microspheres, a value significantly higher than those reported thus far. The possible mechanism for the formation of the microspheres was proposed.     

Synthesis and characterization of Fe3O4@C@Ag nanocomposites and their antibacterial performance

We synthesized Fe₃O₄@C@Ag nanocomposites through a combination of solvothermal, hydrothermal, and chemical redox reactions. Characterization of the resulting samples by X-ray diffraction, Fourier-transform infrared spectroscopy, field-emission scanning and transmission electron microscopy, and magnetic measurement is reported. Compared to Fe₃O₄@Ag nanocomposites, the Fe₃O₄@C@Ag nanocomposites showed enhanced antibacterial activity. The Fe₃O₄@C@Ag nanocomposites were able to almost entirely prevent growth of Escherichia coli when the concentration of Ag nanoparticles was 10 μg/mL. Antibacterial activity of the Fe₃O₄@C@Ag nanocomposites was maintained for more than 40 h at 37 °C. The intermediate carbon layer not only protects magnetic core, but also improves the dispersion and antibacterial activity of the silver nanoparticles. The magnetic core can be used to control the specific location of the antibacterial agent (via external magnetic field) and to recycle the residual silver nanoparticles. The Fe₃O₄@C@Ag nanocomposites will have potential uses in many fields as catalysts, absorbents, and bifunctional magnetic-optical materials.     

Dependence of pH and surfactant effect in the synthesis of magnetite (Fe3O4) nanoparticles and its properties

Nanoparticles of Fe₃O₄ were synthesized by co-precipitation in an aqueous solution containing ferrous and ferric salts (1:2) at varying pH with ammonia as a base. It was found that the value of pH influences the reaction mechanism for the formation of Fe₃O₄. Furthermore, the addition of mercaptoethanol significantly reduced the crystalline size of Fe₃O₄ nanoparticles from 15.03 to 8.02 nm. X-ray diffraction (XRD) spectra revealed that the synthesized nanoparticles were ε-Fe₂O₃ or Fe₃O₄ phase. To further prove the composition of the product, as-prepared Fe₃O₄ were examined by X-ray photoelectron spectroscopy (XPS). Magnetic properties of the obtained particles were determined by vibrating sample magnetometer (VSM). Further analysis of the X-ray studies shows that while maintaining a pH value of 6 and 9 in a solution containing iron salts II and III ions produces ε-Fe₂O₃. Whereas a pH value of 11 produces magnetite (Fe₃O₄) phase. All of these results show that the pH has a major role in the observed phase formation of (Fe₃O₄) nanoparticles.