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.     

Fabrication,physiochemical and optoelectronic characterization of SiO2/CdS core–shell nanostructures

Silica/CdS core–shell nanostructures have been developed using a simple wet chemical route. This method utilizes silica spheres formation followed by successive ionic layer adsorption and reaction method assisted CdS shell layer formation. The morphological studies revealed the uniformity in size distribution with core size of 250 nm and shell thickness of 9 nm. The electron microscopic images also indicate the irregular morphology of CdS shell layer. The structural studies indicate the simple cubic system of CdS shell with no other trace for impurities in the crystal structure. This CdS layer exhibit the band gap energy of 2.66 eV, due to weak quantum confinement and numerous defects presence. The studies on room temperature photoluminescence measurement indicate the emission properties and the corresponding electronic energy levels of defect states. Further, the physiochemical understanding of core–shell formation mechanism clearly matches with the motive behind the defects present in the CdS shell layer.     

Preparation and properties of antibacterial TiO2@C/Ag core–shell composite

Abstract

An environment-friendly hydrothermal method was used to prepare TiO₂@C core–shell composite using TiO₂ as core and sucrose as carbon source. TiO₂@C served as a support for the immobilization of Ag by impregnation in silver nitrate aqueous solution. The chemical structures and morphologies of TiO₂@C and TiO₂@C/Ag composite were characterized by x-ray diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, energy dispersive x-ray spectroscopy and Brunauer–Emmett–Teller (BET) analysis. The antibacterial properties of the TiO₂@C/Ag core–shell composite against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) were examined by the viable cell counting method. The results indicate that silver supported on the surface of TiO₂@C shows excellent antibacterial activity.     

Preparation of polystyrene–polyisoprene core–shell nanoparticles for reinforcement of elastomers

Latex-formed core–shell nanoparticles composed of cross-linked polystyrene (PS) core and polyisoprene (PI) shell were successfully synthesized by means of a two-stage emulsion polymerization. The PS core possessed a Z-average diameter of 50.3 nm, and the PS–PI particles took a spherical shape with a Z-average size of 50–70 nm in diameter. Shell thickness was controlled by varying isoprene loading. Necessary interphase interactions between the core and shell domains were also achieved by grafting and swelling polymerization. Latex compounding method was employed to prepare the filled elastomer compounds. As expected, the PS–PI core–shell nanoparticles exhibited excellent reinforcement to elastomeric matrix, enhancing the tensile strength of the styrene–butadiene rubber by approximately 400%. The lower density, better interfacial interactions, and latex compounding process would benefit the PS–PI nanoparticles reinforced elastomer nanocomposites in energy saving.     

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.     

Preparation and characterization of high-performance Ni-based core–shell catalyst for ethanol steam reforming

Journal of Materials Science - A core–shell catalyst, based on nickel nanoparticles supported on silica nanospheres and surrounded by ceria, was tested for ethanol steam reforming (ESR)...     

Fabrication and fluorescence properties of multilayered core–shell particles composed of quantum dot,gadolinium compound,and silica

A preparation method for multilayered quantum dot/silica/gadolinium compound/silica (QD/Si/Gd/Si) core–shell particles is proposed. Silica (Si)-coated quantum dot (QD/Si) core–shell particles were prepared by a Stöber method at room temperature in water/ethanol solution with TEOS and NaOH in the presence of QD nanoparticles. Succeeding gadolinium compound (Gd)-coating of the QD/Si core–shell particles was performed by a homogeneous precipitation method using Gd(NO₃)₃, urea, and polyvinylpyrrolidone in the presence of the QD/Si particles, which resulted in production of multilayered QD/silica/gadolinium compound (QD/Si/Gd) core–shell particles. For Si-coating of the QD/Si/Gd particles, the Stöber method was performed at room temperature in water/ethanol solution with TEOS and NaOH in the presence of the QD/Si/Gd particles. Consequently, Si-coated QD/Si/Gd, i.e., multilayered QD/Si/Gd/Si, core–shell particles were obtained. The QD/Si/Gd/Si particles revealed strong fluorescence, which was almost comparable to the QD particles with no shells. These particles are expected to be harmless to living bodies, and have dual functions of magnetic resonance imaging and fluorescence.     

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).     

Development of electrosprayed artesunate-loaded core–shell nanoparticles

Objective: Artesunate (ART) is proven to have potential anti-proliferative activities, but its instability and poor aqueous solubility limit its application as an anti-cancer drug. The present study was undertaken to develop coaxial electrospraying as a novel technique for fabricating nanoscale drug delivery systems of ART as the core–shell nanostructures.

Methods: The core–shell nanoparticles (NPs) were fabricated with coaxial electrospraying and the formation mechanisms of NPs were examined. The physical solid state and drug–polymer interactions of NPs were characterized by X-ray powder diffraction (XRPD) and Fourier transform infrared (FTIR) spectroscopy. The effects of materials and electrospraying process on the particle size and surface morphology of NPs were investigated by scanning electron microscopy (SEM). The drug release from NPs was determined in vitro by a dialysis method.

Results: The ART/poly(lactic-co-glycolic) acid (PLGA) chitosan (CS) NPs exhibited the mean particle size of 303?±?93?nm and relatively high entrapment efficiency (80.5%). The release pattern showed an initial rapid release within two hours followed by very slow extended release. The release pattern approached the Korsmeyer–Peppas model.

Conclusions: The present results suggest that the core–shell NPs containing PLGA and CS have a potential as carriers in the anticancer drug therapy of ART.     

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.     

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.     

Structural and optical properties of individual GaP/ZnO core–shell nanowires

Structural and optical properties of ZnO–GaP core–shell nanowires were studied by means of electron microscopy and microphotoluminescence. A thin ZnO shell layer was deposited by RF sputtering on GaP nanowires, which were grown on GaP (111)B substrates under vapour–liquid–solid mode by MOVPE. The SEM and TEM characterization showed that the ZnO shells fully covered the surface of the NWs from top to bottom. Each GaP NW core is composed of many well-defined twinned segments with the planes of twinning oriented in perpendicular to the growth direction. This was contradicted in kinked GaP NWs: their growth direction was initially perpendicular to the twinning planes, but once the NW had kinked, it changed to lie within the twinning planes. The ZnO shell deposited on the GaP core has a columnar morphology. The columns are inclined at a positive angle close to 70° with respect to the GaP growth axis. All observed columns were tilted at this angle to the growth direction. Micro-photoluminescence study showed that thermal annealing improved the quality of the ZnO crystallographic structure; the annealing made observable the photoluminescence peak related to the band-to-band transition in ZnO.     

Preparation and characterization of the carbon–Microsilica composite sorbent

In this paper, Microsilica, one kind of industry solid waste, was utilized firstly to prepare carbon–Microsilica composite sorbent with core–shell structures from a partial carbonization, mixture, and sulfonation process. The prepared composite sorbent was characterized with XPS, FT-IR, SEM, XRD and gas sorption experiments. The characterization results indicated BET surface area (S_BET) and total pore volume (V_total) of the prepared composite sorbent enhance 255% and 136% than Microsilica, respectively, and an abundant of oxygen functional groups, such as carboxyl and sulfonic groups, were introduced into the surface of the prepared composite sorbent. The adsorption capacity of the prepared composite sorbent for methylene blue (MB) and Cr(VI) also was investigated and compared with Microsilica and activated carbon, the results shown that the adsorption capacity of the prepared composite sorbent for methylene blue and Cr(VI) enhance 406.6% and 657.5% than Microsilica, and reach about 70.0% and 72.3% of activated carbon adsorption capacity, respectively. This paper proposed a new approach of comprehensive utilization of Microsilica with a uncomplicated process, and the prepared carbon–Microsilica composite sorbent with excellent adsorbent performance could be used as a potential substitute of activated carbon for heavy metal ion or organic dye adsorption in waste water.     

Preparation of N,N-p-phenylene bismethacryl amide as a novel cross-link agent for synthesis and characterization of the core–shell magnetic molecularly imprinted polymer nanoparticles

Novel magnetic molecularly imprinted nanoparticles (MMIPs) using N,N-p-phenylene bismethacryl amide as a cross linker and super paramagnetic core–shell nanoparticle as a supporter for use in controlled release were prepared by precipitation polymerization. Novel cross-linking agents were synthesized by the reaction of methacryloyl chloride with p-phenylenediamine. Then, the Fe₃O₄ nanoparticles were encapsulated with a SiO₂ shell and functionalized with –CH=CH₂ and MMIPs were further prepared by using methacrylic acid as a functional monomer, N,N-p-phenylene bismethacryl amide as a cross-linking agent and betamethasone as template. Magnetic non-MIPs were also prepared with the same synthesis procedure as with MMIPs only without the presence of the template. The obtained MMIPs were characterized by using transmission electron microscopy, Fourier transform infrared spectrum, X-ray diffraction, energy-dispersive X-ray spectroscopy, and the vibrating sample magnetometer. The performance of the MMIPs for the controlled release of betamethasone was assessed and results indicated that the magnetic MIPs also had potential applications in drug controlled release.     

Dielectric,mechanical and thermal properties of novel core–shell CuPc@MWCNTs/PEN composite films

In this work, multiwalled carbon nanotubes (MWCNTs) were successfully enwrapped by a thin layer of tetra-nitrophthalocyanine copper (CuPc) via solvent-thermal method. EDS spectrum shows that the hybrid materials are mainly composed of C, Cu, N and O elements. TEM images exhibit that the MWCNT was wholly coated with a layer of CuPc and micro-nanoscale core–shell CuPc@MWCNTs were formed. FTIR reveals the detailed chemical groups of micro-nanoscale core–shell CuPc@MWCNTs. Thereafter, CuPc@MWCNTs/polyarylene nitrile ethers (PEN) composite films were prepared via solution-casting method. The CuPc@MWCNTs/PEN composite films possess excellent thermal and mechanical properties endowed by PEN matrix. The glass transition temperature of the composite films is about 175 °C and the initial decomposition temperature is in the range of 494–499 °C. Besides, the tensile modulus of the composite films is above 70 MPa. Furthermore, the dielectric constant of the composite film with 5.0 wt% CuPc@MWCNTs loading is 31 at 50 Hz while the dielectric loss is 0.58 at 50 Hz.     

Bi-layered polymer–magnetite core/shell particles: synthesis and characterization

Polymer magnetic core particles receive growing attention due to these materials owing magnetic properties which are widely used in different applications. The prepared composite particles are characterized with different properties namely: a magnetic core, a hydrophobic first shell, and finally an external second hydrophilic shell. The present study describes a method for the preparation of bi-layered polymer magnetic core particles (diameter range is 50–150 nm). This method comprises several steps including the precipitation of the magnetic iron oxide, coating the magnetite with oleic acid, attaching the first polymer shell by miniemulsion polymerization and finally introducing hydrophilic surface properties by condensation polymerization. The first step is the formation of magnetite nanoparticles within a co-precipitation process using oleic acid as the stabilizing agent for magnetite. The second step is the encapsulation of magnetite into polyvinylbenzyl chloride particles by miniemulsion polymerization to form a magnetic core with a hydrophobic polymer shell. The hydrophobic shell is desired to protect magnetite nanoparticles against chemical attack. The third step is the coating of magnetic core hydrophobic polymer shell composites with a hydrophilic layer of polyethylene glycol by condensation polymerization. Regarding the miniemulsion polymerization the influence of the amount of water, the mixing intensity and the surfactant concentration were studied with respect to the formation of particles which can be further used in chemical engineering applications. The resulting magnetic polymer nanoparticles were characterized by particle size measurement, chemical stability, iron content, TEM, SEM, and IR.     

Ascorbic acid-mediated synthesis and characterisation of iron oxide/gold core–shell nanoparticles.

The current article reports on providing surface modification of magnetic nanoparticles with gold to provide stability against aggregation. Gold-coated magnetite nanoparticles were synthesised to combine both magnetic as well as surface plasma resonance (SPR) properties in a single moiety. The nanocomposites were produced by reduction (using ascorbic acid) of gold chloride on to the surface of iron oxide nanoparticles. Ascorbic acid not only acts as a reducing agent, but also the oxidised form of ascorbic acid i.e. Dehydro-ascorbic acid acts as a capping agent to impart stability to as synthesised gold-coated iron oxide nanocomposites. The synthesised nanocomposite was monodispersed with a mean particle size of around 16 nm and polydispersity index of 0.190. X-ray diffraction analysis confirms presence of gold on the surface of magnetite nanoparticles. The synthesised nanocomposites had a total organic content of around 3.2% w/w and also showed a shifted SPR peak at 546 nm as compared to gold nanoparticles (528 nm). Both uncoated and gold-coated magnetite exhibited superparamagnetic behaviour at room temperature. Upon coating with gold shell, saturation magnetisation of iron oxide nanoparticles decreases from 42.806 to 3.54 emu/gram.     

Investigation of optical properties of core–shell silicon nanowires

The ability to control the size, orientation, composition and morphology of silicon nanowires (SiNWs) presents an ideal platform for exploring a wide range of potential technological applications. In this work, we demonstrated the detail study of optical properties of highly disordered core–shell SiNWs that were grown by atmospheric pressure chemical vapor deposition. The microstructure of SiNWs was characterized by field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM). The TEM study shows that the SiNWs consists of crystalline core silicon surrounded by thick amorphous silicon oxide. The total diameter including the outer SiO₂ sheath was 60–80 nm. The reflection and absorption of a-SiO₂/c-SiNWs were affected by process parameter like silane flow rate and hydrogen dilution. The optical reflection of SiNWs decreased with increasing photon energy across the visible and near the ultraviolet range, approaching moth's eye antireflection. Specifically, a minimum reflection of 2–3% was observed at 400 nm. The band gap is estimated at ∼1.32 eV by quasi-direct band Tauc's plot. The sum of localized states at the band edge is ∼0.53 eV. Straight SiNWs have lower reflection than those of nanoparticles mixed SiNWs and coil mixed SiNWs. The reflection and absorption of SiO₂/SiNWs were confirmed to respond strongly to infrared with increasing H₂ flow rate.     

Preparation of nickel–silver core–shell nanoparticles by liquid-phase reduction for use in conductive paste

Nickel–silver (Ni–Ag) core–shell nanoparticles (NPs) were prepared by depositing Ag on Ni nanocores using the liquid-phase reduction technique in aqueous solution, and their properties were characterised using various experimental techniques. The core–shell NPs had good crystallinity, and the thicknesses of the Ag nanoshells could be tuned effectively. The oxidation resistance of the Ag surface and the electroconductive properties of the Ni core allowed these Ni–Ag core–shell NPs to be used in a conductive paste. Thick films composed of Ni–Ag core–shell NPs were screen-printed on a polycrystalline silicon substrate then sintered at temperatures ranging from 500 °C to 800 °C. Stable resistivity was obtained when the sintering temperature was higher than 650 °C, and the electrical properties of the Ni–Ag core–shell paste were close to those of pure Ag paste. Thus, the Ni–Ag NPs can partly replace pure Ag NPs in conductive pastes.