<Emphasis Type="Italic">In situ</Emphasis> anchor of magnetic Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> nanoparticles onto natural maifanite as efficient heterogeneous Fenton-like catalyst

In situ anchor of magnetic Fe₃O₄ nanoparticles (NPs) onto the surface of natural maifanite was realized by chemical oxidation coprecipitation in hot alkaline solution. The Fe₃O₄/maifanite composites were characterized by XRD, FTIR, SEM, and TEM. These results indicated that polycrystalline Fe₃O₄ NPs with inverse spinel structure were formed and tightly dispersed on maifanite surface. Based on the measurement of surface Zeta potential of maifanite at different medium pHs, the possible combination mechanism between natural maifanite and Fe₃O₄ NPs was proposed. Then, the asobtained composites were developed as highly efficient heterogeneous Fenton-like catalyst for the discoloration of an azo dye, Methyl Orange (MO). The comparative tests on MO discoloration in different systems revealed that Fe₃O₄/maifanite composite exhibited much higher Fenton-like catalytic activity than Fe₃O₄ NPs and the heterogeneous Fentonlike reaction governed the discoloration of MO. Kinetic results clearly showed that MO discoloration process followed the second-order kinetic model. Fe₃O₄/maifanite composites exhibited the typical ferromagnetic property detected by VSM and could be easily separated from solution by an external magnetic field.     

Synthesis and microwave absorption property of ternary composites: polyaniline/CoFe<Subscript>2</Subscript>O<Subscript>4</Subscript>/Ba<Subscript>3</Subscript>Co<Subscript>2</Subscript>Fe<Subscript>24</Subscript>O<Subscript>41</Subscript>

Polyaniline (PANI)/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite was prepared by an in-situ polymerization method. The phase structure, morphology and magnetic properties of the as-prepared PANI/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite were characterized by XRD, FT-IR, SEM, TEM, and VSM, respectively. The microwave absorption properties of the composite were investigated by using a vector network analyzer in the 2–18 GHz frequency range. The results show that the maximum reflection loss value of the PANI/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite reaches ?30.5 dB at 10.5 GHz with a thickness of 3 mm and the bandwidth of reflection loss below ?10 dB reaches up to 1.2 GHz. The excellent microwave absorption properties of the as-prepared PANI/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite due to the enhanced impedance match between dielectric loss and magnetic loss.     

Removal and reuse of Ag nanoparticles by magnetic polyaniline/Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> nanofibers

For the treatment of wastewater containing Ag nanoparticles (NPs), PANI/Fe₃O₄ nanofibers were firstly prepared by a novel self-assemble. And then, the efficiency for the removal of Ag NPs from wastewater was investigated. The magnetic performance of PANI/Fe₃O₄ nanofibers could be optimized by adjusting the pH of the self-assemblied system. Under pH of 3, the as-prepared nanofibers exhibited the highest magnetism and also displayed good efficiency (>?12 mg g^?1) for the removal of Ag NPs. Importantly, the resulted product (PANI/Fe₃O₄/Ag composite) could act as a catalysis for cleaning durable pollutant, 4-nitrophenol. After 10 cycles, only slight decrease in rate constant was found, indicating excellent reusability. Those approaches provide a new way to merge the recovery of Ag NPs as pollutants and reuse of recovered Ag NPs as recyclable material for environmental remediation.     

Lightweight glass/Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>-polyaniline composite hollow spheres with conductive and magnetic properties

Lightweight composite hollow spheres with conductive and magnetic properties were prepared by using Hollow Glass Spheres (HGS) as substrate. The morphology, composition, conductive, and magnetic properties of the resultant products were characterized by SEM, EDX, XRD, FTIR spectra, conductivity measurement, and vibrating-sample magnetometry. Polyaniline (PANI) were in situ polymerized on HGS with increasing ratios of PANI to HGS, resulting in the enhanced conductivity of HGS/PANI composites from 1.3 × 10⁻² S/cm to 4.4 × 10⁻² S/cm. Lightweight glass/Fe₃O₄-PANI composite hollow spheres (HGS/Fe₃O₄-PANI) with conductivity of 5.4 × 10⁻³ S/cm and magnetization of 9.25 emu/g were prepared by deposition of Fe₃O₄ nanoparticles onto HGS via electrostatic adsorption first, and then polymerization of aniline onto HGS/Fe₃O₄. The glass/PANI-Fe₃O₄ composite hollow spheres (HGS/PANI-Fe₃O₄) composed of Fe₃O₄ as the outmost layer and PANI as the inner layer were prepared for comparison. The conductivity and magnetization of HGS/PANI-Fe₃O₄ were 1.1 × 10⁻⁴ S/cm and 2.61 emu/g, respectively.     

Fast microwave synthesis of Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> and Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>/Ag magnetic nanoparticles using Fe<Superscript>2+</Superscript> as precursor

A simple and quick microwave method to prepare high performance magnetite nanoparticles (Fe₃O₄ NPs) directly from Fe has been developed. The as-prepared Fe₃O₄ NPs product was fully characterized by X-ray diffraction, transmission electron microscopy and scanning electron microscopy. The results show that the as-prepared Fe₃O₄ NPs are quite monodisperse with an average core size of 80 × 5 nm. The microwave synthesis technique can be easily modified to prepare Fe₃O₄/Ag NPs and these NPs possess good magnetic properties. The formation mechanisms of the NPs are also discussed. Our proposed synthesis procedure is quick and simple, and shows potential for large-scale production and applications for catalysis and biomedical/biological uses.     

Direct synthesis of mesoporous Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> through citric acid-assisted solid thermal decomposition

A simple and inexpensive approach to synthesizing mesoporous Fe₃O₄ is developed by using citric acid-assisted solid thermal decomposition of ferric nitrate. The structure and magnetic property of mesoporous Fe₃O₄ were characterized by XRD, FT–IR, N₂ adsorption–desorption isotherms, TEM, and vibrating sample magnetometer. It was shown that the decomposition of citric acid results in the formation of the mesoporous structure and narrow pore-size distribution. The reducing atmosphere which created by the decomposition of the ferric nitrate–citric acid complex caused the partial reduction of Fe(III) to Fe(II) and in turn the formation of Fe₃O₄. Moreover, the strength of the coordination between carboxyl group and Fe³⁺ also affected the phase composition of the iron oxides.     

Magnetically separable Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>@TiO<Subscript>2</Subscript> nanospheres: preparation and photocatalytic activity

A facile and efficient approach for the fabrication of Fe₃O₄@TiO₂ nanospheres with a good core–shell structure has been demonstrated. Products were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectra (XPS), X-ray diffraction (XRD) and vibrating sample magnetometer (VSM). The results showed that Fe₃O₄@TiO₂ nanocomposites exhibited high degree of crystallinity, excellent magnetic properties at room temperature. Furthermore, the as-prepared Fe₃O₄@TiO₂ nanocomposites exhibited good photocatalytic activity toward the degradation of Rhodamine B (RhB) solution. Additionally, the recycling experiment of Fe₃O₄@TiO₂ nanocomposites had been done, demonstrating that Fe₃O₄@TiO₂ nanocomposites have high efficiency and stability.     

The synthesis and the magnetic properties of Sm<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>BiY<Subscript>2–<Emphasis Type="Italic">x</Emphasis></Subscript>Fe<Subscript>5</Subscript>O<Subscript>12 </Subscript>nanoparticles

Sm _x BiY_2–x Fe₅O₁₂ (x = 0, 0.1, 0.2, 0.4, 0.6, 0.8) nanocrystals were fabricated by sol–gel method. Samples were characterized by powder X-ray diffraction (XRD), thermal gravity analysis (TGA) and differential thermal analysis (DTA), transmission electron microscopy (TEM), vibrating sample magnetometer(VSM). The samples were calcined at 850 °C and 1000 °C and the average size of the particles were determined by Scherrer’s formula . In this paper, we discussed the effect of Sm³⁺ substitution for Y³⁺ on magnetic properties of BiY₂Fe₅O₁₂. The magnetic properties of Sm _x BiY_2−x Fe₅O₁₂ are decreased with increasing content of Sm ion.     

Synthesis and application of TiO<Subscript>2</Subscript>/SiO<Subscript>2</Subscript>/Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> nanoparticles as novel adsorbent for removal of Cd(II), Hg(II) and Ni(II) ions from water samples

In the current study, SiO₂/Fe₃O₄ core–shell nanoparticles functionalized with TiO₂, using a simple method and application for removal of Cd(II), Hg(II) and Ni(II) ions from aqueous solution. The structure of the resulting product was confirmed by X-ray diffraction spectrometry, transmission electron microscopy (TEM), pH_pzc and Brunauer, Emmett and Teller methods. The average diameter of TiO₂/SiO₂/Fe₃O₄ nanoparticles according to TEM was obtained around 48 nm. In batch tests, the effects of pH, initial metal concentration, contact time and temperature were studied. Adsorption of metal ions was studied from both kinetics and equilibrium point of view. Maximum adsorption capacity of Cd(II), Hg(II) and Ni(II) on TiO₂/SiO₂/Fe₃O₄ nanoparticles was 670.9, 745.6 and 563.0 mg g^?1, respectively. Adsorption–desorption results showed that the reusability of nanoparticles was encouraging. This adsorbent was successfully applied to removal Cd(II), Hg(II) and Ni(II) ions in real samples including tap water, electronic wastewater and medical wastewater.     

Preparation and characteristic of magnetic LDPE/Fe3O4 nano-composite films

Magnetic LDPE/Fe₃O₄ composite films have been successfully prepared using conventional melt blending technique in a sigma internal mixer. The magnetic Fe₃O₄ nanoparticles using in compositing were perpared by chemical co-precipitation method and characterized by TEM, XRD, FTIR and their magnetism was analyzed by VSM. The LDPE/Fe₃O₄ composite films were measured with SEM, XRD, FTIR and VSM. The magnetic measurement showed that both the Fe₃O₄ nanoparticles and the composite films made through doping of Fe₃O₄ nanoparticles in original LDPE displayed a super-paramagnetic property. And other results showed that the composite films were dispersed homogeneously and the structure of original LDPE were not destroyed with the doping of Fe₃O₄ nanoparticles.     

Magnetic properties of Nd-Y<Subscript>3</Subscript>Fe<Subscript>5</Subscript>O<Subscript>12</Subscript> nanoparticles

Nb³⁺-substituted garnet nanoparticles Y_3−xNd_xFe₅O₁₂ (x = 0.0, 0.5, 1.0, 1.5, and 2.0) were fabricated by a sol-gel method and their crystalline structures and magnetic properties were investigated by using X-ray diffraction (XRD), thermal analysis (DTA/TG), and vibrating sample magnetometer (VSM). The XRD patterns of Y_3−xNd_xFe₅O₁₂ have only peaks of the garnet structure and the sizes of particles range from 34 to 70 nm. From the results of VSM, it is shown that when the Nd concentration x ( 1.0, the saturation magnetization of Y_3−xNd_xFe₅O₁₂ increases as the Nd concentration (x) is increased, and gets its maximum at x = 1.0, but when x ( 1.0, the saturation magnetization decreases with increasing the Nd concentration (x), this may be due to the distortion of the microstructure of Y_3−xNd_xFe₅O₁₂, which leads to the decrease of the effective moment formed by Fe³⁺. Meanwhile, it is observed that with the enhancement of the surface spin effects, the saturation magnetization rises as the particle size is increased.     

Study on the endocytosis and the internalization mechanism of aminosilane-coated Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> nanoparticles in vitro

In this study, the endocytosis and the internalization mechanism of aminosilane-coated Fe₃O₄ nanoparticles into human lung cancer cell line SPC-A1 was studied compared with human lung cell line WI-38 in vitro. The particle endocytosis behavior was studied by using Transmission Electron Microscope (TEM) and Coupled Plasma-Atomic Emission Spectrometry (ICP-AES). It was found that aminosilane-coated Fe₃O₄ nanoparticles could be greatly taken up by SPC-A1 human cancer cells (202 pg iron/cell) but not by WI-38 human lung cells (13 pg iron/cell). The particles could be retained in SPC-A1 cells over a number of generations in vitro. Different endocytosis was observed by TEM after SPC-A1 cells were treated with different temperature or with/without Cytochalasin B (Inhibitor of phagocytosis) at 37 °C. No nanoparticles were taken up by SPC-A1 after the endocytosis inhibited in low temperature. Restoring the endocytosis activity at 37 °C, the process of nanoparticles from coated pit to endosomes and lysosomes was observed by TEM. Endocytosis activity was effectively inhibited by the presence of Cytochalasin B at 37 °C, while a lot of nanoparticles were uptaken to the cytoplasm of SPC-A1 cells in the control group. Our results suggest that the process of endocytosis of aminosilane-coated Fe₃O₄ nanoparticles can efficiently takes place in lung cancer cells and nanoparticles can be kept in cancer cells for generations. Phagocytosis may be involved in the internalization process of aminosilane-coated Fe₃O₄ nanoparticles.     

Structural studies of a new electroceramic composite: Pb(Fe<Subscript>0.5</Subscript>Nb<Subscript>0.5</Subscript>)O<Subscript>3</Subscript> (PFN)-Cr<Subscript>0.75</Subscript>Fe<Subscript>1.25</Subscript>O<Subscript>3</Subscript>(CRFO)

A study of the structural characteristics of the composites [Pb(Fe_0.5Nb_0.5)O₃(PFN)] _x -[Cr_0.75Fe_1.25O₃(CRFO)]_100?x (x = 0 (CRFO100), 10, 50, 90, 100) was performed in this work. The compounds PFN100 and CRFO100 were prepared by conventional solid-state method and investigated by X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and ⁵⁷Fe Mössbauer Spectroscopy techniques. The X-ray analysis shows that PFN100 is tetragonal and the CRFO100 phase has a trigonal symmetry. The refinement of all the composites was also performed and discussed in this paper. The Mössbauer spectrum for the composite samples shows a paramagnetic doublet and a sextet probably assigned to a magnetic phase associated to Fe⁺³. For the sample PFN100, only a magnetic field of 49.5 T (isomer shift (δ) = 0.21 mm/s) was detected. For the composite sample, the δ and Δ are typical of Fe ions at sites of octahedral coordination.     

Heterogeneous Fenton-like discoloration of methyl orange using Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>/MWCNTs as catalyst: combination mechanism and affecting parameters

Multi-walled carbon nanotubes (MWCNTs) can act not only as a support for Fe₃O₄ nanoparticles (NPs) but also as a coworker with synergistic effect, accordingly improving the heterogeneous Fenton-like efficiency of Fe₃O₄ NPs. In this study, Fe₃O₄ NPs were in situ anchored onto MWCNTs by a moderate co-precipitation method and the as-prepared Fe₃O₄/MWCNTs nanocomposites were employed as the highly efficient Fenton-like catalysts. The analyses of XRD, FTIR, Raman, FESEM, TEM and HRTEM results indicated the formation of Fe₃O₄ crystals in Fe₃O₄/MWCNTs nanocomposites prepared at different conditions and the interaction between Fe₃O₄ NPs and MWCNTs. Over a wide pH range, the surface of modified MWCNTs possessed negative charges. Based on these results, the possible combination mechanism between Fe₃O₄ NPs and MWCNTs was discussed and proposed. Moreover, the effects of preparation and catalytic conditions on the Fenton-like catalytic efficiency were investigated in order to gain further insight into the heterogeneous Fenton-like reaction catalyzed by Fe₃O₄/MWCNTs nanocomposites.     

Light weight RGO/Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> nanocomposite for efficient electromagnetic absorption coating in X-band

Reduced graphene oxide (RGO)/magnetite (Fe₃O₄) nanocomposite has been synthesized by an in-situ facile hydrothermal method. The XRD pattern reveals the development of nanocomposite in which both phases are coexistent. Raman Spectroscopy shows the main characteristics peaks of D and G bands at 1349 cm^?1 and 1595 cm^?1 for graphitic structures. The intensity ratio (I_D/I_G) is also calculated, which indicate the degree of defects in the material. This ratio (I_D/I_G), increases from 0.84 for GO to 0.91 for RGO/Fe₃O₄ nanocomposite and promotes the defects which are beneficial for electromagnetic (EM) absorption. The SEM image depicts that, Fe₃O₄ spherical nanoparticles are dispersed over the surface of graphene sheets and provide a thermal conducting path for heat dissipation between different layers of graphene. The EM absorption properties have been analyzed at 2–18 GHz of RGO and RGO/Fe₃O₄. The addition of proper content of Fe₃O₄ magnetic nanoparticles in RGO sheets improved the Reflection Loss (RL) from ??13.5 dB to ??20 dB at a frequency of 9.5 GHz. Moreover, due to magnetic loss and interfacial polarization, the effective bandwidth increases from 2.5 GHz to 3.8 GHz at a coating thickness of 1.5 mm. Hence this light weight nanocomposite is an excellent material for strong EM absorption in X-band.     

Synthesis and applications of fluorescent-magnetic-bifunctional dansylated Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>@SiO<Subscript>2</Subscript> nanoparticles

Bifunctional magnetic-luminescent dansylated Fe₃O₄@SiO₂ (Fe₃O₄@SiO₂-DNS) nanoparticles were fabricated by the nucleophilic substitution of dansyl chloride with primary amines of aminosilane-modified Fe₃O₄@SiO₂ core–shell nanostructures. The morphology and properties of the resultant Fe₃O₄@SiO₂-DNS nanoparticles were investigated by transmission electron microscopy, FT–IR spectra, UV–vis spectra, photoluminescence spectra, and vibrating sample magnetometry. The Fe₃O₄@SiO₂-DNS nanocomposites exhibit superparamagnetic behavior at room temperature, and can emit strong green light under the excitation of UV light. They show very low cytotoxicity against HeLa cells and negligible hemolysis activity. The T ₂ relaxivity of Fe₃O₄@SiO₂-DNS in water was determined to be 114.6 Fe mM⁻¹ s⁻¹. Magnetic resonance (MR) imaging analysis coupled with confocal microscopy shows that Fe₃O₄@SiO₂-DNS can be uptaken by the cancer cells effectively. All these positive attributes make Fe₃O₄@SiO₂-DNS a promising candidate for both MR and fluorescent imaging applications.     

Radiation Synthesis and Magnetic Property Investigations of the Graft Copolymer Poly(Ethylene-g-Acrylic Acid)/Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> Film

In this work, acrylic acid (AAc) monomer was grafted onto low-density polyethylene (LDPE) films by the direct method to obtain acid (LDPE-grafted poly(acrylic acid) (LDPE-g-PAAc)) graft copolymers. The presence of the grafted PAAc with COOH groups allows coupling with Fe^2+/3+ ions. The stabilization of Fe₃O₄ particles onto the graft copolymers was done by in situ reduction of LDPE-g-PAAc/Fe^2+/3+ with sodium borohydride (NaBH₄) in aqueous solution. The LDPE-g-PAAc graft copolymer and LDPE-g-PAAc/Fe₃O₄ composite films were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC), and electron spin resonance (ESR). The synthesized composites exhibit excellent magnetic properties. The results indicated that the magnetic oxide (Fe₃O₄) was embedded and homogenously dispersed into the surfaces of the graft copolymer films as indicated by SEM. The FT-IR analysis clearly suggests that an AAc monomer was effectively grafted onto LDPE. The XRD studies elucidate the change in the crystallinity of the graft copolymers.

Open image in new window

Graphical Abstract The procedures for magnetic film manufacture LDPE-g-PAAc/Fe₃O₄ using gamma irradiation technique

     

Structural,Magnetic, Optical,and Catalytic Properties of Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> Nanoparticles by the Sol-Gel Method

This article was aimed to extend a simple procedure for the preparation by a sol-gel method by using iron nitrate and polar solvent (e.g., water) as the starting materials from the viewpoint that they are of low cost. A study of the effect of chelating agents such as citric acid weight ratio on the structure of Fe₃O₄ was reported. The synthesized product was characterized by powder X-ray diffraction (XRD), high-resolution scanning electron microscopy (HR-SEM), high-resolution transmission electron microscopy (HR-TEM), photoluminescence (PL) studies, and vibrating sample magnetometer (VSM). Magnetic analysis revealed that the Fe₃O₄ nanoparticles had a ferromagnetic behavior at room temperature with a saturation magnetization of 20.83 emu/g. Furthermore, Fe₃O₄ nanoparticles prepared by the sol-gel method using citric acid were tested for the catalytic activity towards the oxidation of benzyl alcohol.     

An Investigation of Y<Subscript>3</Subscript>Ba<Subscript>5</Subscript>Cu<Subscript>8</Subscript>O<Subscript>18</Subscript> Doping with Ag Nanoparticles and Its Application as Superconductor

Y₃Ba₅Cu₈O₁₈ superconductors were prepared through a standard solid-state reaction and the structural properties of the samples were studied through XRD and the Rietveld refinement method. The effect of silver nanoparticles doping on the Y₃Ba₅Cu₈O₁₈ superconductors was studied as well. It is known that the size of nanoparticles is increased during aging. Therefore, two batches of samples with 1 and 2 wt% of Ag nanoparticles and the size range of 30, 200, 500, 700, 800, and 1000 nm were prepared. After preparing the samples and observing the Meissner effect, the crystallography, critical current density, critical temperature, magnetic susceptibility, SEM, and EDX experiments of the samples were carried out. The results of the critical current density measurements showed that the sample with 2 wt% Ag nanoparticles and the size of 700 nm has the maximum current density. In both batches of samples, increasing the nanoparticle size to 700 nm led to an increase in the critical current density. The crystallography studies showed that silver nanoparticles do not insert into the superconductor’s frame. Actually, they are placed in the samples as a distinct phase.     

Novel preparation of ultrafine MnCo<Subscript>1.75</Subscript>Fe<Subscript>0.25</Subscript>O<Subscript>4</Subscript> nanostructures for the photodegradation of Acid Red 88

For the first time, ultrafine MnCo_1.75Fe_0.25O₄ nanostructures were prepared via a novel coprecipitation–calcination route by using tetraethylenepentamine (tepa) and SDBS as precipitating agent and surfactant, respectively. Results of this study show that particle size and morphology of the MnCo_1.75Fe_0.25O₄ samples can be controlled by setting main reaction parameters such as reaction temperature, surfactant type and calcination temperature. The as-prepared MnCo_1.75Fe_0.25O₄ nanostructures were characterized by EDX, TEM, FESEM, VSM, FT-IR, XRD and UV–Vis analysis. The photocatalytic degradation of the acid red 88 dye as water pollutant was performed to examine the photocatalytic performance of as-prepared MnCo_1.75Fe_0.25O₄ nanostructures.