Catalytic properties of silica/silver nanocomposites

The catalytic properties of silver nanoparticles supported on silica and the relation between catalytic activity of silver particles and the support (silica) size are investigated in the present article. The silver nanoparticles with 4 nm diameters were synthesized and were attached to silica spheres with sizes of 40, 78, 105 nm, respectively. The reduction of Rhodamine 6G (R6G) by NaBH4 was designed by using the SiO2/Ag core-shell nanocomposites as catalysts. The experimental results demonstrated that the catalytic activity of silica/silver nanoparticles depends on not only the concentration of catalysts (silver) but also the support silica size. Silver particles supported on small SiO2 spheres (approximately 40 nm) show high catalytic activity. Moreover, by making a comparison between the UV-vis spectra of the catalyst before and after the catalytic reaction, we found that the position of surface plasma resonance (SPR) peak of Ag nanoparticles changes little. The above results suggested that the size and morphology of silver particles were probably kept unchanged after the reduction of R6G and also implied that the catalytic activity of silver particles was hardly lost during the catalytic reaction.     

Evaluating the potential of nanoparticles for controlling zinc stearate release from low‐density polyethylene into food simulants

The present study addressed the effect of polymer nanocomposites with different loading contents of fume silica (nanospheres) and nanoclay (nanosheet) on migration of zinc stearate from packaging materials into food simulants. Specific migration levels of zinc stearate from neat low‐density polyethylene (LDPE) and LDPE/nanocomposites into two food simulants stored at 40°C for 10 days were determined by gas chromatography coupled with flame ionization detector. Differential scanning calorimetry (DSC) analysis showed that incorporation of nanoparticles, especially at 1 wt% loading level of nano silica, noticeably increased degree of crystallinity, which significantly reduced water vapour permeability. Nanocomposites had a lower migration of zinc stearate in comparison with neat polymer. Additionally, results of this study revealed that physical properties of the food simulant had dominant effect on migration of zinc stearate.     

Preparation and application of magnetic cobalt/SiO2 core/shell nanospheres

Homogeneous SiO₂-coated cobalt nanospheres with tunable silica shell thickness from 21.7 nm to 4.5 nm were synthesized by using modified Stöber method. These nanocomposites were used as source materials to prepare SiO₂ semi-hollow and hollow nanospheres by partially and completely etching cobalt cores, respectively. A proposed formation mechanism of these Co/SiO₂ nanospheres with a core/shell structure was presented in this paper, which is also important for the rational design and synthesis of other monodisperse core/shell nanoarchitectures with uniform size and shape. Furthermore, these Co/SiO₂ nanospheres were also used as a substrate for the deposition of CdS nanocrystals to prepare magnetic luminescent Co/SiO₂/CdS nanocomposites.     

In situ growth of CoPt nanoparticles in porous germania nanospheres

Mesoporous nanospheres of germania were used as matrix to grow CoPt nanoparticles. The host germania nanospheres were prepared by biomineralization via the recognition of the peptide sequence T-G-H-Q-S-P-G-A-Y-A-A-H. The size of the cobalt/platinum nanoparticles embedded in germania is in the 8-9 nm range, as determined by TEM analysis. The porosity of the nanocomposites was confirmed by nitrogen isotherm analysis. MFM analysis confirmed the magnetic properties of the germania nanocomposites. This simple method of preparation of germania nanospheres via biomineralization, followed by growth of CoPt nanoparticles has an attractive potential for preparing new optomagnetic materials. Such nanocomposites for various device fabrications can be produced and potentially be used to target specific applications.     

Silica fluorescent nanospheres containing a large amount of quantum dots prepared using liposomes as templates

Quantum dot (QD) fluorescent spheres have captivated many scientists because of their many potential applications in biomedical research. In this work, QD nanospheres were prepared using a novel method: incorporating QDs into nano-liposomes and then synthesising a silica shell using a lipid membrane as the template. The results showed that the nanocomposites obtained were spherical in shape, and each nanosphere contained a silica shell and the cores consisted of a large amount of QDs. Ultrathin sections of the spheres showed that the thickness of the silica shell was about 50–60?nm. Because the QD cores were coated with liposome and thick silica shell, the bright field of the silica sphere suspension was close to milk white in colour, which was different from that of the red-coloured QD solution. Although the quantum yield of the silica spheres (2.27%) was lower than that of the QDs (23.52%), these nanospheres still emitted a bright fluorescence, and there was no obvious difference between the fluorescent colour of the nanosphere suspension and the QD solution.     

Surface-enhanced Raman spectroscopy studies of orderly arranged silica nanospheres-synthesis,characterization and dye detection

Silica nanospheres have been explored much for drug delivery, photocatalysis, sensors and energy storage applications. It also acts as a template for Surface-Enhanced Raman Spectroscopy (SERS) substrates. Uniform nanostructures at low cost with high reproducibility are the major challenges in SERS substrate fabrication. In the present work, silica nanospheres were synthesized using stober method and deposited on to glass slides using Vertical deposition techniques. Different size/thickness of Silver (Ag) nanoparticles were deposited onto silica thin films using sputter deposition technique. The monodispersity of silica nanospheres and size of silver nanoparticles (10 nm, 20 nm and 30 nm) were confirmed by FESEM analysis. The structural properties were confirmed through XRD. UV–Vis analysis revealed that the plasmonic properties of Ag@SiO₂ give high surface plasmons for 30 nm thickness of silver. The binding energy of Ag@SiO₂ confirmed through XPS spectrum. The fabricated SERS substrates were used to detect Rhodamine 6G (R6G), Methylene blue (MB), Methylene violet (MV) and Methyl orange dyes as an analyte molecule with a limit of detection at about 10^?11 mol/L. The addition of SiO₂ nanospheres decreases the Ag oxidation rate and increases their stability. The maximum enhancement factor (1.5?×?10⁷) achieved for 30nm thickness of Ag@SiO₂. The results and technique establish the potential applications and reproducible SERS substrate.

     

Size-dependent surface plasmon resonance in silver silica nanocomposites

Silver silica nanocomposites were obtained by the sol-gel technique using tetraethyl orthosilicate (TEOS) and silver nitrate (AgNO(3)) as precursors. The silver nitrate concentration was varied for obtaining composites with different nanoparticle sizes. The structural and microstructural properties were determined by x-ray diffractometry (XRD), Fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). X-ray photoelectron spectroscopic (XPS) studies were done for determining the chemical states of silver in the silica matrix. For the lowest AgNO(3) concentration, monodispersed and spherical Ag crystallites, with an average diameter of 5?nm, were obtained. Grain growth and an increase in size distribution was observed for higher concentrations. The occurrence of surface plasmon resonance (SPR) bands and their evolution in the size range 5-10?nm is studied. For decreasing nanoparticle size, a redshift and broadening of the plasmon-related absorption peak was observed. The observed redshift and broadening of the SPR band was explained using modified Mie scattering theory.     

Preparation of silver nanoparticles with antimicrobial activities and the researches of their biocompatibilities

Silver nanoparticles were prepared by chemical reduction method using chitosan as stabilizer and ascorbic acid as reducing agent in this work. The silver/chitosan nanocomposites were characterized in terms of their particle sizes and morphology by using UV spectrophotometer, nano-grainsize analyzer, and transmission electron microscopy. Antibacterial activities of these nanocomposites were carried out for Staphylococcus aureus and Escherichia coli. The silver nanoparticles exhibited significantly inhibition capacity towards these bacteria. Detailed studies on the biocompatibility of the silver/chitosan nanocomposites were investigated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and cell adhesion test. The results indicated that these silver/chitosan nanocomposites were benefit for the proliferation and adhesion of L-929 cells, and the biocompatibilities between the nanocomposites and the cells would become better with the culturing days. We anticipated that these silver/chitosan nanocomposites could be a promising candidate as coating material in biomedical engineering and food packing fields wherein antibacterial properties and biocompatibilities are crucial.     

Study on gelatin-silver nanoparticle composite towards the development of bio-based antimicrobial film

Nano-scale silver particle stabilized by gelatin protein was prepared through the reduction of aqueous silver nitrate solution by sodium borohydride. Gelatin concentration was varied against a fixed concentration of silver nitrate to optimize the gelatin to metal ratio. Gelatin-protected Ag-nanoparticle was characterized by UV-VIS spectroscopy and transmission electron microscopy (TEM). All the samples exhibited similar yellow color with a characteristic plasmonic band of silver nanoparticles at 412 nm. TEM micrographs also showed the presence of nanoscale silver particles of approximately 3.9 nm. Since silver has strong bactericidal properties and at the same time relatively less toxic to human cell, silver in various forms is ideally suited for a wide range of applications in consumer, industrial and medical products The antimicrobial properties of gelatin-silver nanocomposites were tested by 'cup-plate zone of inhibition' method. The nanocomposites exhibited significant antibacterial and antifungal activity.     

Synthesis and characterization of high-purity silica nanosphere from rice husk

The work reports the synthesis, characterization, and the properties of high-purity silica nanospheres from low-cost rice husk. Primarily, the rice husk was washed with distilled water (DW) and subjected to acid leaching to remove the impurities. The treated rice husk was annealed at different temperatures (620 and 900 degrees C) for varied time periods to achive the desirable silica nanospheres. The annealing temperature and time considerably affected the properties of the synthesized silica nanospheres. The morphology studies confirmed that the size of nanospheres were of approximately 50-60 nm. The photoluminesence studies revealed that the synthesized silica nanospheres showed less structural defects and good optical properties. On the basis of the formation and the characterization of silica nanospheres a possible mechanism was suggested. Inductively coupled plasma mass spectrometry (ICP-MS) analysis confirmed that the synthesized silica nanospheres contained approximately 99.93% purity.     

中空二氧化硅纳米球的制备与应用研究进展

中空二氧化硅纳米球是一种具有单个空腔或多个空腔,直径在纳米级的新型结构材料。目前已开发出多种中空二氧化硅纳米球的制备方法,不同制备方法各具差异性。中空二氧化硅纳米球在医学、保温隔热和光学等多领域中有广泛应用。对模板法、喷雾干燥法、选择性刻蚀法等多种中空二氧化硅纳米球的制备方法及其特点进行了梳理和分析,评价了其优缺点,并探讨了中空二氧化硅纳米球的应用进展。     

Incorporation of silver nanoparticles coated with mercaptosuccinic acid/poly(ethylene glycol) copolymer into epoxy for enhancement of dielectric properties

A novel route to the synthesis of polymer-coated silver nanoparticles (NPs) was developed on the basis of the reduction of Tollens' reagent using mercaptosuccinic acid/poly(ethylene glycol) (MSA/PEG) copolymer as reducing agent and stabilizer simultaneously. The average size of the polymer-coated silver NPs could be controlled in a wide range from 10 to 120 nm by changing the MSA/PEG molar ratio. These surface-coated silver NPs can be uniformly dispersed in polar solvent and a homogeneous silver NPs/acetone dispersion has been prepared. Silver–epoxy nanocomposites have been developed by incorporating these silver NPs into epoxy. The nanocomposites with silver volume content of 25% showed a more than 3000% increase in dielectric constant as compared to neat matrix and a relatively low dielectric loss below 0.05, which meets the main requirement for embedded decoupling capacitors. Moreover, thermal properties of the silver–epoxy nanocomposites were also characterized by thermogravimetric analysis (TGA) and dynamic mechanical thermal analysis (DMTA). The initial decomposition temperature and glass transition temperature were elevated with the increase of silver content, which exhibit great thermal stability and facilitate electrical applications requiring higher heat-resistance.     

Structure-property relationship in sol-gel derived polymer/silica hybrid nanocomposites prepared at various pH

This paper reports a comparative study on structure-property relationship of acrylic rubber (ACM)/silica, epoxidised natural rubber (ENR)/silica and poly (vinyl alcohol) (PVA)/silica hybrid nanocomposites prepared by sol-gel technique under different pH levels (pH = 1.0–13.0), probably for the first time. The initial concentration of tetraethoxysilane (TEOS) (used as the precursor for silica) was kept at 45 wt%, and tetrahydrofuran (THF) for ACM/silica and ENR/silica while water for PVA/silica were taken as solvents. TEOS to water mole ratio was maintained at 1:2 for the rubber/silica systems to accomplish the sol-gel reaction. The structure of the resultant hybrid composites was determined by using electron microscopy, Fourier Transform infrared spectroscopy and solubility. Dynamic mechanical and mechanical properties were also investigated. The silica particles were found to exist as nanoparticles (average diameter <100 nm) at low pH (≤ 2.0) beyond which these aggregate, although the amount of silica generation was not strictly influenced by the various pH conditions in all the systems. These nanocomposites were optically clear and showed superior mechanical reinforcement over the micro-composites containing aggregated silica structures with lower optical clarity. The nanocomposites exhibited higher storage modulus both at the glassy and the rubbery regions as compared to those micro-composites. The loss tangent peak heights were also minimum and the Tg shifted to higher temperature for those nanocomposites. The maximum improvement of mechanical properties was observed with the PVA/silica nanocomposites due to higher level of interaction between the hydroxyl groups of PVA and the silanol groups of the silica phase.     

Pd Nanosheet‐Covered Hollow Mesoporous Silica Nanoparticles as a Platform for the Chemo‐Photothermal Treatment of Cancer Cells

A versatile system combining chemotherapy with photothermal therapy for cancer cells using Pd nanosheet‐covered hollow mesoporous silica nanoparticles is reported. While the hollow mesoporous silica core can be used to load anticancer drugs (i.e., doxorubicin) for chemotherapy, the Pd nanosheets on the surface of particles can convert NIR light into heat for photothermal therapy. More importantly, the loading of Pd nanosheets on hollow mesoporous silica nanospheres can dramatically increase the amount of cellular internalization of the Pd nanosheets: almost 11 times higher than the unloaded Pd nanosheets. The as‐prepared nanocomposites efficiently deliver both drugs and heat to cancer cells to improve the therapeutic efficiency with minimal side effects. Compared with chemotherapy or photothermal therapy alone, the combination of chemotherapy and phototherapy can significantly improve the therapeutic efficacy, exhibiting a synergistic effect.     

Structural analysis of graphene oxide/silver nanocomposites: optical properties,electrochemical sensing and photocatalytic activity

In the present study, graphene oxide/silver (GO/Ag) nanocomposites were synthesized via a facile simple one pot chemical reduction method using ethylene glycol/sodium borohydrate (EG/NaBH₄) as solvent and reducing agent. GO was selected as a substrate and stabilizer to prepare GO/Ag nanocomposites. The synthesized GO/Ag nanocomposites were characterized by a series of techniques. Highly monodispersed stable crystalline silver nanoparticles having a face-centered cubic (fcc) phase were confirmed by X-ray powder diffraction (XRD) on GO signature. Scanning electron microscopy images showed that Ag nanoparticles are deposited on the GO sheet with a narrow size distribution. Transmission electron microscopy observations revealed that large numbers of Ag nanoparticles were uniformly distributed on GO sheet and well separated with an average size of 18 nm. Ultraviolet–visible (UV–Vis) spectroscopic results showed the peak of GO and surface plasmon resonance (SPR) of Ag nanoparticles. The SPR property of GO/Ag nanocomposites showed that there was an interaction between Ag nanoparticles and GO sheet. The intensities of the Raman signal of GO/Ag nanocomposites are gradually increased with attachment of Ag nanoparticles i.e. there is surface-enhanced Raman scattering activity. Electrochemical investigations indicated that the nanocomposites possessed an excellent performance for detecting towards 4-nitrophenol. An application of the obtained GO/Ag nanocomposites as a catalyst in the reduction of 4-nitrophenol to 4-aminophenol by NaBH₄ was demonstrated. The GO/Ag nanocomposites exhibited high activity and stability for the catalytic reduction of 4-nitrophenol. The prepared GO/Ag nanocomposites act as photo-catalysts.     

Directly ultraviolet photochemical deposition of silver nanoparticles on silica spheres: Preparation and characterization

A simple method was developed to directly deposit silver nanoparticles on the surface of silica spheres. The photochemical reduction was carried out by ultraviolet irradiation in air atmosphere at room temperature. The [Ag(NH₃)₂]⁺was reduced to silver atoms upon ultraviolet irradiation. Silver atoms subsequently deposited on the surface of silica spheres and agglomerated into silver nanoparticles. Silica spheres with silver nanoparticles of different size and density can be simply controlled by adjusting the UV-light irradiation time. The silver nanoparticles deposited on silica spheres were characterized by X-ray photoelectron spectroscopy, X-ray diffraction, transmission electron microscopy, and field emission scanning electron microscopy.     

Monodisperse porphyrin nanospheres synthesized by coordination polymerization

Monodisperse nanospheres are formed by coordination polymerization tetrakis(4-pyridyl)porphyrin-metal complexes with chloroplatinic acid in aqueous solution. The porphyrin nanospheres and their platinized nanocomposites have potential applications in catalysis and solar energy conversion systems.     

Candidate mechanisms controlling the electrical characteristics of silica/XLPE nanodielectrics

The incorporation of silica nanoparticles into polyethylene has been shown to increase the breakdown strength significantly compared to composites with micron scale fillers. Additionally, the voltage endurance of the nanocomposites is two orders of magnitude higher than that of the base polymer. The most significant difference between micron-scale and nano-scale fillers is the large interfacial area in nanocomposites. Because the interfacial region (interaction zone) is likely to be pivotal in controlling properties, this paper compares the behavior of nanoscale silica/cross-linked low density polyethylene nanocomposites with several silica surface treatments. In addition to breakdown strength and voltage endurance, dielectric spectroscopy, absorption current measurements, and thermally stimulated current determinations (TSC) were performed to elucidate the role of the interface. It was found that a reduction in the mobility in nanocomposites as well as a change in the defect size may be key to explaining the improvement in the properties.     

Fabrication and characterization of Ag-SiO2 composite hollow nanospheres

Ag-SiO₂ composite hollow nanospheres were synthesized by impregnation of hollow silica nanospheres (HSNSs), which were prepared by templating CaCO₃ nanoparticles, in [Ag(NH₃)₂]NO₃ aqueous solution followed by heat treatment. The straightforward process generates composite materials containing Ag nanoparticles, with the average size of 6–10 nm in diameter, uniformly dispersed and mainly distributed on the shells or between the spaces of the HSNSs. The Ag-supported HSNSs were characterized through TEM, EDS, and XPS. Furthermore, ASS, XRD and UV-Vis analyses demonstrated that higher loading efficiency could be achieved under the optimum loading conditions of a silver precursor solution of 0.08 M, pH = 9.0 and HSNSs with a BET surface area of 830.4 m²/g.     

Facial synthesis of polypyrrole/silver nanocomposites at the water/ionic liquid interface and their electrochemical properties

Polpyrrole (PPy)/silver nanocomposites with their size of around 80-120 nm were successfully synthesized at the interface of water and ionic liquid. High dispersed PPy/silver nanocomposites were obtained in the presence of polyvinylpyrrolidone (PVP) by controlling the reacting conditions. The morphology and structure of the resulting nanocomposites were characterized by transmission electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction and X-ray photoelectron spectroscopy. It was also found that the electrical conductivity of PPy/silver nanocomposites was much higher than that of pure PPy. Cyclic voltammetric experiments further indicated that the nanocomposite had excellent redox ability: polypyrrole; silver; ionic liquid; interface synthesis; and nanocomposites.