Preparation and characterization of structure-tailored magnetic fluorescent Fe3O4/P(GMA–EGDMA–NVCz) core–shell microspheres

Fe₃O₄ nanoparticles were prepared by solvothermal reaction, and structure-tailored Fe₃O₄/poly(glycidyl methacrylate-ethyleneglycol dimethacrylate-N-vinylcarbazole) (Fe₃O₄/P(GMA–EGDMA–NVCz)) core–shell microspheres were achieved by distillation–precipitation polymerization of GMA, EGDMA, and NVCz in the presence of Fe₃O₄ nanoparticles. The properties of Fe₃O₄/P(GMA–EGDMA–NVCz) microspheres were characterized by transmission electron microscopy(TEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), vibrating sample magnetometry (VSM), and fluorescence spectroscopy. The results showed that the size of Fe₃O₄/P(GMA–EGDMA–NVCz) core–shell microspheres could be controlled to 930–470 nm by adjusting the amount of shell monomers, corresponding magnetic content of 45–82 wt%, and saturation magnetization of 32–63 emu/g. Moreover, the intensity of the fluorescence increased considerably with the decrease of shell thickness and the increase of NVCz concentration in the monomer mixture.     

Synthesis and characterisation of Ni-doped Fe3O4/polypyrrole magnetic and conducting nanocomposites with core–shell structure

Abstract

Electrical and magnetic function materials have many potential applications. A magnetic and conducting Ni-doped Fe₃O₄/polypyrrole (PPy) nanocomposite with a core–shell structure was prepared by in situ polymerisation of a pyrrole monomer in an aqueous solution containing a dispersion of Ni-doped Fe₃O₄ nanoparticles. The structure and properties of Ni-doped Fe₃O₄/PPy nanocomposites were characterised by X-ray diffraction (XRD), TEM, infrared spectrometry (IR), vibrating sample magnetometry (VSM) and thermogravimetry (TG). The results showed that the Ni-doped Fe₃O₄ nanoparticles were completely coated by polypyrrole; the resultant Ni-doped Fe₃O₄/PPy nanocomposites exhibited a good superparamagnetic behaviour and the saturation magnetisation was as high as 25·2 emu g^?1 owing to the adoption of Ni-doped Fe₃O₄ as the magnetic source. In addition, the influences of Ni-doped Fe₃O₄ content on the electromagnetic properties of resultant nanocomposites were preliminarily investigated.     

Synthesis and characterization of quaternized carboxymethyl chitosan/poly(amidoamine) dendrimer core–shell nanoparticles

With the aim to develop a novel water-soluble modified chitosan nanoparticle with tuned size and improved antibacterial activity, quaternized carboxymethyl chitosan/poly(amidoamine) dendrimers (CM-HTCC/PAMAM) were synthesized. Firstly low-generation amino-terminated poly(amidoamine) (PAMAM) dendrimers were prepared via repetitive reactions between Michael addition and amidation, which were then employed for modifying quaternized carboxymethyl chitosan (CM-HTCC). Prior to the reaction of CM-HTCC with PAMAM, carboxylic groups in CM-HTCC were activated with EDC/NHS in order to enhance the reaction efficiency. FT-IR, ¹H NMR, elemental analysis and XRD were performed to characterize CM-HTCC/PAMAM dendrimers. Turbidity measurements showed that CM-HTCC/PAMAM dendrimers had good water-solubility. TEM images indicated that CM-HTCC/PAMAM dendrimers existed as smooth and spherical nanoparticles in aqueous solution. The results of antibacterial activity explored that CM-HTCC/PAMAM dendrimer nanoparticles displayed higher antibacterial activity against Gram-negative bacteria Escherichia coli (E. coli), whereas they showed much less efficiency against Gram-positive bacteria Staphylococcus aureus (S. aureus) compared to quaternized chitosan (HTCC).     

Synthesis and characterization of Fe–B nanoparticles for potential magnetic applications

The crystallization and structure of Fe–B nanoparticles (NPs) of different sizes formed in a single process by gas aggregation from Fe₈₀B₂₀ targets were analyzed by transmission electron microscopy. It is concluded that all NPs are covered by an amorphous Fe–B shell while the crystal structure of the NPs core depends on their size. Large NPs with diameters ≥30 nm are monocrystalline tetragonal Fe₃B, small diameter NPs (≤20 nm) are completely amorphous whereas in middle size NPs, with diameters between 20 and 30 nm, difference Fe–B phases (tetragonal Fe₃B and orthorhombic FeB) together with defaulted areas are observed. This work opens new possibilities to produce Fe–B NPs tailoring their magnetic properties by controlling their size and composition.     

Synthesis,characterization and bactericidal activity of silica/silver core–shell nanoparticles

Silica/silver core–shell nanoparticles (NPs) were synthesized by coating silver NPs on silica core particles (size ~300 ± 10 nm) via electro less reduction method. The core–shell NPs were characterized for their structural, morphological, compositional and optical behavior using X-ray diffraction, scanning electron microscopy, energy dispersive X-ray analysis and UV–Visible spectroscopy, respectively. The size (16–35 nm) and loaded amount of silver NPs on the silica core were found to be dependent upon reaction time and activation method of silica. The bactericidal activity of the NPs was tested by broth micro dilution method against both Bacillus subtilis (gram positive) and Escherichia coli ATCC25922 (gram negative) bacterium. The bactericidal activity of silica/silver core–shell NPS is more against E. coli ATCC25922, when compared to B. subtilis. The minimal inhibitory concentration of the core–shell NPs ranged from 7.8 to 250 μg/mL and is found to be dependent upon the amount of silver on silica, the core. These results suggest that silica/silver core–shell NPs can be utilized as a strong substitutional candidate to control pathogenic bacterium, which are otherwise resistant to antibiotics, making them applicable in diverse medical devices.     

Synthesis of maghemite (γ-Fe2O3) nanoparticles by thermal-decomposition of magnetite (Fe3O4) nanoparticles

In this research work, we prepared γ-Fe₂O₃ nanoparticles by thermal-decomposition of Fe₃O₄. The Fe₃O₄ nanoparticles were synthesized via co-precipitation method at room temperature. This simple, soft and cheap method is suitable for preparation of iron oxide nanoparticles (γ-Fe₂O₃; Fe₃O₄). The samples were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), vibrating sample magnetometer and differential scanning calorimeter (DSC). The XRD and FT-IR results indicated the formation of γ-Fe₂O₃ and Fe₃O₄ nanoparticles. The TEM images showed that the γ-Fe₂O₃ and Fe₃O₄ were spherical, and their size was 18 and 22 nm respectively. Magnetic properties have been measured by VSM at room temperature. Hysteresis loops showed that the γ-Fe₂O₃ and Fe₃O₄ nanoparticles were super-paramagnetic.     

Synthesis and characterization of core–shell magnetic molecularly imprinted polymer nanoparticles for selective extraction of tizanidine in human plasma

In this study, simple, effective and general processes were used for the synthesis of a new nano-molecularly imprinted polymers (MIPs) layer on magnetic Fe₃O₄ nanoparticles (NPs) with uniform core–shell structure by combining surface imprinting and nanotechniques. The first step for the synthesis of magnetic NPs was co-precipitation of Fe²⁺ and Fe³⁺ in an ammonia solution. Then, an SiO₂ shell was coated on the magnetic core with the Stöber method. Subsequently, the C=C groups were grafted onto the silica-modified Fe₃O₄ surface by 3-(trimethoxysilyl) propyl methacrylate. Finally, MIPs films were formed on the surface of Fe₃O₄@SiO₂ by the copolymerization of C=C end groups with methacrylic acid (functional monomer), ethylene glycol dimethacrylate (cross-linker), 2,2-azobisisobutyronitrile (initiator) and tizanidine (template molecule). The products were characterized using techniques that included Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), thermo gravimetric analysis (TGA), scanning electron microscopy (SEM), UV spectrophotometry, transmission electron microscopy (TEM) and vibrating sample magnetometer (VSM). Measurement of tizanidine through use of the core–shell magnetic molecularly imprinted polymers nanoparticles (MMIPs-NPs) in human plasma samples compared to the paracetamol showed that the synthesized nanosized MMIP for tizanidine has acted selectively.     

Preparation of magnetite core–shell nanoparticles of Fe3O4 and carbon with aryl sulfonyl acetic acid

High quality Fe₃O₄/carbon core–shells and shell–core nanoparticles have been successfully synthesized by depositing an epitaxial growth of Fe₃O₄ or carbon shell onto carbon or Fe₃O₄ nanocore. By employing the agents such as aryl sulfonyl acetic acid and glucose, Fe₃O₄ and carbon in a nanoscale was prepared from iron aryl sulfonyl acetate and then by the solvothermal reaction of glucose in a reverse microemulsion. The advantages of present approach rely not only on its simplicity, rapidity, and efficiency of the procedure, but also the formation of the controlled core–shell structures as well. It is highly suitable for further applications. Different core–shell structure controls could be attained by careful adjustment of the procedure sequences of decarboxylation and solvothermal reaction. The magnetic studies show that Fe₃O₄/carbon core–shell and shell–core nanoparticles found to be superparamagnetic. The characteristic differences in the core–shell structures would lead to the change of magnetization behaviors of Fe₃O₄ nanoparticles.     

Fe3O4 and CdS based bifunctional core–shell nanostructure

A room temperature solution process for synthesis of Fe₃O₄ nanoparticles and their hybrid core shell nanostructures using CdS as the shell material has been described. The as grown particles have been characterised using XRD, Rietveld refinement, high resolution transmission electron microscopy, atomic force microscopy, superconducting quantum interference device, optical absorbance and photoluminescence spectroscopy. A superparamagnetic response revealed from the magnetisation measurements of the as synthesised magnetite nanoparticles was retained even after the growth of the CdS shell. From luminescence and high resolution atomic force microscopy measurements, it is shown that the core–shell structures advantageously combine magnetic as well as fluorescence response with a tendency towards self-organization.     

Synthesis and characterization of core–shell nanoparticles and their influence on the mechanical behavior of acrylic bone cements

Core–shell nanoparticles consisting of polybutyl acrylate (PBA) rubbery core and a polymethyl methacrylate (PMMA) shell, with different core–shell ratios, were synthesized in order to enhance the fracture toughness of the acrylic bone cements prepared with them. It was observed by TEM and SEM that the core–shell nanoparticles exhibited a spherical morphology with ca. 120 nm in diameter and that both modulus and tensile strength decreased by increasing the PBA content; the desired structuring pattern in the synthesized particles was confirmed by DMA. Also, experimental bone cements were prepared with variable amounts (0, 5, 10 and 20 wt.%) of nanoparticles with a core–shell ratio of 30/70 in order to study the influence of these nanostructured particles on the physicochemical, mechanical and fracture properties of bone cements. It was found that the addition of nanostructured particles to bone cements caused a significant reduction in the peak temperature and setting time while the glass transition temperature (T_g) of cements increased with increasing particles content. On the other hand, modulus and strength of bone cements decreased when particles were incorporated but fracture toughness was increased.     

Synthesis and characterization of core–shell SiO2@(Er3+,Yb3+):Lu2O3

We synthesized crystalline Erbium Er³⁺ and Ytterbium Yb³⁺ codoped -Lu₂O₃ nanolayers on SiO₂ microspheres using the modified Pechini method. Two different kinds of precursors, nitrates and chlorides, have been used leading to a layer-to-layer morphology and necklaces structures, respectively. In both cases, the size of nanocrystallites constituting the optical active layer is around 5 nm. We performed X-ray powder diffraction to confirm the cubic crystalline structure of the sesquioxides layer. High resolution transmission electron microscopy analyses corroborate the crystalline nature of the layer. The optical emission of Er³⁺ in the visible range has been recorded.     

Synthesis of Al/Fe3Al core–shell intermetallic nanoparticles by chemical liquid deposition method

In this work, an Al/Fe₃Al core–shell nanoparticle was obtained by heat treatment of a precursor in high purity of argon. The precursor, with Fe(CO)₅ and nano Al as raw materials, was synthesized simply by a chemical liquid deposition method. The evolution of the phase and morphology during the heat-treatment has been carefully studied by XRD and TEM. The results indicate that the precursor transformed to core–shell structure of Fe₃Al intermetallic nanoparticle. The formation of the Fe₃Al intermetallic nanoparticle was explored by DSC test, which reveals that the formation temperature of the nanoparticle is around 587 °C. Moreover, the TG–DSC measurements from 50 °C to 1000 °C in compressed air (20% O₂ and 80% N₂) reveal that the heat-treated powder of the precursor remains thermal stability in relatively low temperature but becomes concentrated combustion in elevated temperature.     

Surfactant assisted synthesis and multifunctional features of Fe3O4@ZnO@SiO2 core–shell nanostructure

In this study, hybrid core–shell magnetic nanostructure comprising Fe₃O₄ core with multiple shells of zinc oxide and silica having well defined morphologies are produced by a simple synthetic approach based on an effective chemical precipitation technique. Semi-solid and hydrophilic poly ethylene glycol was used as the stabilizing agent to control the particle size of the magnetic nanostructures. 1-Hexadecyltrimethyl ammonium chloride was employed as the surfactant to achieve the core–shell nanostructure. The formation of the core–shell nanostructures were confirmed by X-ray diffraction, Fourier transform infra-red spectroscopy and high resolution transmission electron microscopy respectively. We also observed the pronounced ferromagnetic features of ZnO coated Fe₃O₄ core–shell nanostructure that substantiates the magnetization reversal mechanism of the spinel magnetite. The coating of dense SiO₂ on Fe₃O₄@ZnO was found to shift the magnetic behaviour from ferromagnetic to super-paramagnetic even at room temperature. The optical features of the material are observed by UV–Vis Spectrometer and Photoluminescence spectrometer.     

Thermal stress dependence of magnetic hysteretic processes in core–shell nanoparticles

The control of thermal stresses in the core–shell structures is an important task in order to understand their temperature dependent magnetization processes. This paper is dedicated to a theoretical and micromagnetic study of the thermal stresses on the hysteretic processes in core–shell nanoparticles. The analytical model can predict the thermal and elastic behavior of the core–shell nanoparticle supposed to a forced cooling process. The temperature and thermal stresses values obtained by direct computation from the analytical model were used to evaluate the magneto-elastic energy of the core–shell system. A micromagnetic model was used to compute the equilibrium positions of the particle magnetization as function of the applied field. The model allows an evaluation of the increase of the particle coercive field and of the blocking temperature as an effect of the thermal stress.     

Synthesis of Au@CdS core–shell nanoparticles and their photocatalytic capacity researched by SERS

High-quality Au@CdS core–shell nanoparticles (CSNs) have been synthesized to improve photo-conversion efficiency in photocatalysis. They demonstrate higher photocatalytic activity in the experiment of photocatalytic degradation of rhodamine 6G (R6G) solution than that of CdS counterparts. Au@CdS CSNs can broaden the absorption range in visible region compared to CdS counterparts. The heterojunction interface between Au and CdS facilitates the separation of photo-generated electron–hole pairs, and transfers electrons from CdS region to Au core. The two advantages are crucial to improve the photocatalytic activity of Au@CdS CSNs. Charge transfer mechanism between metal and semiconductor is efficient that can be used to guide the design of photocatalysts, photovoltaics, and other optoelectronic devices to effectively utilize the solar power. In this paper, we research the photocatalytic process by surface-enhanced Raman scattering (SERS). The combination of photocatalysis and SERS not only can show the change in concentration of R6G solution, but also can provide the information of the change of R6G molecular structure in photocatalytic process.     

Synthesis and characterization of Co–Fe nanoparticles supported on mesoporous silicas

Co–Fe bimetallic samples containing 25 wt% total of metal content were prepared by incipient wetness impregnation of cobalt nitrate and iron nitrate salts over hexagonal mesoporous silica (HMS) and SBA-15 supports. Changes in the textural properties and reduction behavior were compared with monometallic cobalt/iron-based samples. The samples were characterized by N₂ physisorption, X-ray diffraction (XRD), H₂-temperature programmed reduction (TPR), transmission electron microscopy (TEM) and H₂ chemisorption. The amount of incorporated metal was estimated by atomic absorption spectroscopy (AAS). Morphological properties revealed that after introduction of the metal to the SBA-15 support, the specific area, pore volume and pore diameter decreased to a lesser extent for bimetallic samples. XRD measurements detected the formation of Co₃O₄ and CoFe₂O₄ phases for both bimetallic samples. TPR profiles indicated similar behavior for both the bimetallic and monometallic samples. Higher temperatures were observed for the reducibility of Co–Fe/HMS as compared to Co–Fe/SBA-15. Dispersion values of the bimetallic samples were higher than Fe monometallic samples and lower than Co monometallic samples according to hydrogen chemisorption. The particle size distribution of the bimetallic samples estimated by TEM microphotographs showed a smaller fraction of larger size particles for Co–Fe/SBA-15.     

Controllable synthesis and characterization of Ag@AgBr core–shell nanowires

Ag@AgBr core–shell nanowires have been synthesized in large quantities via a redox reaction between Ag nanowires and FeBr₃ in solution at room temperature. The effect of the molar ratio of Fe:Ag on the formation and optical absorption of the Ag@AgBr core–shell nanowires was systematically studied. The results showed that Ag nanowires were converted into Ag@AgBr core–shell nanowires and finally into AgBr nanorods with the increase of the molar ratio of Fe:Ag. At the same time, the optical absorption of Ag nanowires decreased gradually and disappeared finally. In addition, the growth mechanism of the Ag@AgBr core–shell nanowires was also discussed in detail.     

Preparation, characterization, and fluorescence properties of well-dispersed core–shell CdS/carbon nanoparticles

The core–shell CdS-carbon (CdS/C) nanoparticles were synthesized for the first time via a facile pyrolysis approach of bis(β-mercaptoethanol)-cadmium(II) as a single-source precursor. After using acid treatment method, well-dispersed and homogeneous core–shell CdS/C nanoparticles were obtained. The morphology, structure, and properties of CdS/C nanoparticles were investigated by X-ray diffraction (XRD), Raman spectra, transmission electron microscopy, X-ray photoelectron spectroscopy (XPS), and fluorescence spectroscopy. Most of the prepared nanoparticles presented core–shell structures with core diameter of ~10 nm and shell thickness of ~4 nm. The CdS core belonged to hexagonal crystal system. The carbon shell was employed as a good dispersion medium to form well-dispersed small sized CdS particles. XRD and XPS results revealed that there is an interaction between CdS core and carbon shell. Fluorescence measurement showed that the monodispersed CdS-carbon nanoparticles exhibit remarkable fluorescence enhancement effect compared with that of the pristine CdS nanoparticles, which indicates the prepared nanoparticles are a promising photoresponsive material.