Preparation, Electrochemical Property and Application in Bulk-modified Electrode of Dawson-type Phospho-molybdate-doped Polypyrrole Composite Nanoparticles

A kind of inorganic-organic hybrid semiconductor composite nanoparticles： Dawson-type phosphomolybdate- doped polypyrrole （P2Mo18-PPy） was designed and prepared using microemulsion oxidation-polymerization at room temperature and characterized by TEM and IR. The P2Mo18-PPy was used as a bulk-modifier to fabricate a chemically modified carbon paste electrode（CPE） by direct mixing, which represents the example of polyoxometalates（ POMs）- doped semiconductor polymer nanoparticles modified electrode. Both the advantage of POMs-doped polymer and the surface-renewal property of the CPE were fully utilized. The electrochemical behavior of the P2Mo18-PPY bulk-modified CPE（P2Mo18-PPy-CPE） was investigated with cyclic voltammetry. Three couples of reversible redox peaks were observed in the range from ＋ 800 to 0 mV, which corresponded to the reduction and oxidation through two-, four- and six-electron processes, respectively. The P2 Mo18-PPY-CPE showed a high electrocatalytic activity for the reduction of nitrite, which expanded the application of POMs-doped semiconductor polymer nanoparticles.

PREPARATION OF POLYSTYRENE/SiO_2 COMPOSITE NANOPARTICLES BEARING SULFONIC GROUPS ON THE SURFACE VIA EMULSION COPOLYMERIZATION USING A POLYMERIZABLE EMULSIFIER

Functionalized PS/SiO_2 composite nanoparticles bearing sulfonic groups on the surface were successfully synthesized via emulsion copolymerization using a polymerizable emulsifierαolefin solfonate(AOS).As demonstrated by transmission electron microscopy and atomic force microscopy,well-defined core-shell PS/SiO_2 composite nanoparticles with a diameter of 50 nm were obtained.Sulfonic groups introduced onto the surface of the composite nanoparticles were quantified by FTIR,and can be controlled to some exten...

Synthesis and characterization of Fe_3O_4@SiO_2 magnetic composite nanoparticles by a one-pot process

Fe3O4@SiO2 core–shell composite nanoparticles were successfully prepared by a one-pot process. Tetraethyl-orthosilicate was used as a surfactant to synthesize Fe3O4@SiO2 core–shell structures from prepared Fe3O4 nanoparticles. The properties of the Fe3O4 and Fe3O4@SiO2 composite nanoparticles were studied by X-ray diffraction, transmission electron microscopy, energy dispersive spectroscopy, and Fourier transform infrared spectroscopy. The prepared Fe3O4 particles were approximately 12 nm in size, and the thickness of the SiO2 coating was approximately 4 nm. The magnetic properties were studied by vibrating sample magnetometry. The results show that the maximum saturation magnetization of the Fe3O4@SiO2 powder（34.85 A·m^2·kg^–1） was markedly lower than that of the Fe3O4 powder（79.55 A·m^2·kg^–1）, which demonstrates that Fe3O4 was successfully wrapped by SiO2. The Fe3O4@SiO2 composite nanoparticles have broad prospects in biomedical applications; thus, our next study will apply them in magnetic resonance imaging.

Preparation and characterization of cross-linked β-cyclodextrin polymer/Fe_3O_4 composite nanoparticles with core-shell structures

Cross-linkedβ-cyclodextrin polymer/Fe3O4 composite nanoparticles with core-shell structures were prepared via cross linking reaction on the surface of carboxymethylβ-cyclodextrin（CM-β-CD） modified Fe3O4 nanoparticles inβ-cyclodextrin alkaline solution by using epichlorohydrin as crosslinking agent.The morphology,structure and magnetic properties of the prepared composite nanoparticles were investigated by transmission electron microscopy（TEM）,Fourier transform infrared（FTIR） spectrometry,X-ray diffraction（XRD） measurement,thermogravimetric analysis（TGA） and Vibrating sample magnetometry （VSM）,respectively.

Composite magnetic nanoparticles:Synthesis and cancer-related applications

Recent advances in the preparation and applications of composite magnetic nanoparticles are reviewed and summa- rized, with a focus on cancer-related applications.

Microstructure and abrasive wear behaviour of anodizing composite films containing Si C nanoparticles on Ti6Al4V alloy

Anodized composite films containing Si C nanoparticles were synthesized on Ti6Al4 V alloy by anodic oxidation procedure in C4O6H4Na2 electrolyte. Scanning electron microscopy(SEM), energy dispersive spectroscopy(EDS) and X-ray photoelectron spectroscopy(XPS) were employed to characterize the morphology and composition of the films fabricated in the electrolytes with and without addition of Si C nanoparticles. Results show that Si C particles can be successfully incorporated into the oxide film during the anodizing process and preferentially concentrate within internal cavities and micro-cracks. The ball-on-disk sliding tests indicate that Si C-containing oxide films register much lower wear rate than the oxide films without Si C under dry sliding condition. Si C particles are likely to melt and then are oxidized by frictional heat during sliding tests. Potentiodynamic polarization behavior reveals that the anodized alloy with Si C nanoparticles results in a reduction in passive current density to about 1.54×10-8 A/cm2, which is more than two times lower than that of the Ti O2 film(3.73×10-8 A/cm2). The synthesized composite film has good anti-wear and anti-corrosion properties and the growth mechanism of nanocomposite film is also discussed.

Direct Electrochemistry and Electrocatalysis of Hemoglobin at PAMAM Dendrimer-MWNTs-Au Nanoparticles Composite Film Modified Glassy Carbon Electrode

The direct electron transfer of hemoglobin at the PAMAM-MWNTs-AuNPs composite film modified glassy carbon electrode was studied. In a phosphate buffer solution（PBS, pH=7.0）, the formal potential（E^0） of Hb was -0.105 V versus SCE, the electron transfer rate constant was 4.66 s-1. E^0＇ of Hb at the modified electrode was linearly varied in a pH range of 5.0-8.0 with a slope of-49.2 mV/pH. The Hb/PAMAM-MWNTs-AuNPs/GCE gave an excellent electrocatalytic response to the reduction of hydrogen peroxide. The catalytic current increased linearly with H2O2 concentration in a range of 1.0× 10^-6 to 2.2× 10^-3 mol/L. The detection limit was 2.0× 10^-7 mol/L at a signal to noise ratio of 3. The Michaelis-Menten constant（Km^app） was 2.95 mmol/L.

Study on the Properties of MetaIIophthalocyanine-Fe_3O_4 Nanoparticles Composite

The solubility , antioxidation ability, thermal stability, coercivity Hc and long term stability of MPc-Fe3O4-nanoparticles composite(M=Co, Cu, Ni, Mn) have been studied. The results show that MFc-Fe3O4 nanoparticles composite can be easily dissolved in dilute acid. The dissolving rate of different MPc-Fe3O4 nanoparticles composite is in the following order:M=Mn-M = Co<M=Cu<M=Ni. The antioxidation ability of Fe3O4 nanoparticles are improved greatly after their complex with MPc and there is good relationship between Toxidation of Fe3O4 nanoparticles and n , the complex layers of MPc on the surface of the composite. The results also show that the thermal stability of Fe3O4 nanoparticles increases greatly and the Hc ot them decreases dramatically after Fe3O4 nanoparticles form nanoscale composite with MPc. MPc-Fe3O4 nanoparticles composite have high long term stability.

Graphene-gold Nanoparticle Composite Film Modified Electrode for Determination of Trace Mercury in Environmental Water

The graphene-gold nanoparticles composite film modified glassy carbon electrode （EG- AuNPs/GCE） was prepared by one-step coelectrodeposition and employed for determination of trace mercury in environmental water with differential pulse stripping voltammetry. Such a nanostructured composite film combined with the advantages of gold nanoparticles and graphene, can greatly promote the electron-transfer process and increase accumulation abil-ity for Hg（Ⅱ）, leading to a remarkably improved sensitivity. The linear calibration curve ranged from 0.2 μg/L to 30 μg/L for Hg（Ⅱ） and the detection limit （S/N=3） was found to be 0.03 μg/L at a deposition time of 300 s. Moreover, the stablity of the as-prepared electrode and interferences from other substances were evaluated. The modified electrode was successfully applied to the direct detection of Hg（Ⅱ） in real water samples.

PREPARATION, COMPLEX MECHANISM AND STRUCTURE MODEL OF METALLOPHTHALOCYANINE-Fe_3O_4 NANOPARTICLES COMPOSITE

MPc-Fe3O4-nanoparticles composite(M= Co, Cu , Ni, Mn ) have been prepared and the factors that influence their mean size have been studied. The mean size of the nanoparticles composite increase with the increase of complex temperature. The interaction of MPc with Fe3O4 nanoparticles has been studied. There are M-O covalent bonding and ionic bonding between MPc and Fe3Q4 nanoparticles. The intensities of M-O bonding and ionic bonding are in vestigated . The complex mechanism of MPc with Fe3O4 nanoparticles have been studied. First, there are complex between MPc and all Fe3O4 nanoparticles. Then, Fe3O4 nanoparticles accumulate together to form the accumulators, MPc have the function of cohering Fe3O4 nanoparticles. A considerable number of MPc combine with Fe3O4 nanoparticles on the surface of the accumu-lators to form MPc-Fe3O4 nanoparticles composite. All the above proesses take place spontaneously. The structuremodel of MPc-Fe3O4 nanoparticles composite has also been investigated. Inside the MPc-Fe3O4 nanoparticles composite, Fe3O4 nanoparticles accumulate together without order, on the surface of the composite, MPc form molecular dispersion layer. The threshold of molecular dispersion layer are also investigated.

Polypyrrole Chitosan Cobalt Ferrite Nanoparticles Composite Layer for Measuring the Low Concentration of Fluorene Using Surface Plasmon Resonance

Fluorene is a polycyclic aromatic hydrocarbon, which is a hazardous toxic chemical in the environment. The measurement of low concentrations of fluorene is a subject of intense interest in chemistry and in the environment. Polypyrrole chitosan cobalt ferrite nanoparticles are prepared using the electrochemical method. The prepared layers are characterized using field emission scanning electron microscopy, Fourier transform infrared spectroscopy, and energy dispersive spectroscopy. The layers are used to detect fluorene using the surface plasmon resonance technique at room temperature. The composite layer is evaluated after detection of fluorene using atomic force microscopy. The fluorene is bound on the layer, and the shift of the resonance angle is about 0.0052°, corresponding to the limitation of 0.01 ppm.

The Effects of Nanoparticle Additives on Thermophysical Properties of Concrete Mixtures

In recent years, energy-retrofitting is becoming an imperative aim for existing buildings worldwide and increased interest has focused on the development of nanoparticle blended concretes with adequate mechanical properties and durability performance, through the optimization of concrete permeability and the incorporation of the proper nanoparticle type in the concrete matrix. In order to investigate the potential use of nanocomposites as dense barriers against the permeation of liquids into the concrete, three types of nanoparticles including Zinc Oxide (ZnO), Magnesium Oxide (MgO), and composite nanoparticles were used in the present study as partial replacement of cement. Besides, the effect of adding these nanoparticles on both pore structure and mechanical strengths of the concrete at different ages was determined, and scanning electron microscopy (SEM) images were then used to illustrate the uniformity dispersion of nanoparticles in cement paste. It was demonstrated that the addition of a small number of nanoparticles effectively enhances the mechanical properties of concrete and consequently reduces the extent of the water permeation front. Finally, the behavioral models using Genetic Algorithm (GA) programming were developed to describe the time-dependent behavioral characteristics of nanoparticle blended concrete samples in various compressive and tensile stress states at different ages.

Tailoring the Meso-Structure of Gold Nanoparticles in Keratin-Based Activated Carbon Toward High-Performance Flexible Sensor

Flexible biosensors with high accuracy and reliable operation in detecting pH and uric acid levels in body fluids are fabricated using well-engineered metaldoped porous carbon as electrode material.The gold nanoparticles@N-doped carbon in situ are prepared using wool keratin as both a novel carbon precursor and a stabilizer.The conducting electrode material is fabricated at 500℃ under customized parameters,which mimics A-B type(two different repeating units) polymeric material and displays excellent deprotonation performance(pH sensitivity).The obtained pH sensor exhibits high pH sensitivity of 57 mV/pH unit and insignificant relative standard deviation of 0.088%.Conversely,the composite carbon material with sp^2 structure prepared at 700℃ is doped with nitrogen and gold nanoparticles,which exhibits good conductivity and electrocatalytic activity for uric acid oxidation.The uric acid sensor has linear response over a range of 1-150 μM and a limit of detection 0.1 μM.These results will provide new avenues where biological material will be the best start,which can be useful to target contradictory applications through molecular engineering at mesoscale.

Synthesis and Characterization of Natural Polymer/Inorganic Antibacterial Nanocomposites

In order to increase antibacterial abilities and avoid the aggregation of nanoparticle, Ag- ZnO nanocomposites were studied in the network structure which contains bonds, and these bonds are formed by hydrolysis reaction between Ti（TBOU）4（TBOT） and the water that in Persimmon tannin solution. The size and morphology of Ag-ZnO nanocompos：tes were investigated by scanning electron microscopy （SEM） and field emission scanning electron microscopy（FE-SEM）. The antibacterial properties of nanocomposites were examined by minimal bactericidal concentration（MBC）. Results showed that this kind of antibacterial nanocomposites composites（ANPs） have excellent antibacterial abilities and without aggregation.

Nonlinear Optieal Properties of Ag Nanopartieles/Glass Composites Measured on a Femtosecond Time Scale

Ag nanoparticles embedded in soda-lime silicate glass were fabricated by ion-exchange and subsequently annealing method. Effects of annealing duration on the optical nonlinearity and ultrafast dynamics of Ag nanoparticles in glass were investigated by z-scan technique and pump-probe technique. The results indicate that the third-order optical nonlinearity increases with extending the annealing time, the fast decay process with lifetime of a few picoseconds is attributed to thermal equilibrium process of hot electrons and the energy transfer to lattices by interaction with phonons in the formed Ag nanoparticles, while the slow decay in more than one hundred picoseconds corresponds to the subsequent cooling process by a thermal diffusion from the Ag nanoparticle to the host matrix via the phonon-medium interaction. The fast decay process is accelerated with extending the annealing time.

Synthesis and Tribological Properties of Copper-alumina Nanocomposites Prepared by Coprecipitation Technique

The objective of this work is to study the synthesis of copper-alumina nanocomposites using the coprecipitation process and hot-pressing method, and investigate their mechanical properties. The effects of calcination temperature on the average size of composite particles and chemical composition after calcination were also analyzed. The sintering parameters including sintering temperature, hot pressure and packing time were optimized to fabricate the alumina nanoparticles reinforced copper matrix composites（CMCs）. The density, microhardness and tribological properties of the CMCs reinforced with 1 wt%, 2 wt%, 3 wt%, 4 wt% and 5 wt% of alumina nanoparticles were investigated correspondingly. The results showed that the optimum preparation parameters for the CMCs were 900 ℃ of hot pressing temperature, 27.5 MPa of hot pressure and 2 hrs of packing time. The CMC reinforced with 2 wt% of alumina nanoparticles had the lowest wear rate, with the relative wear resistance of 3.13.

Shape and size effects of ceria nanoparticles on the impact strength of ceria/epoxy resin composites

Ceria nanoparticles with various shapes （rods, cubes, and plates） and sizes were controllably synthesized and then introduced into epoxy resin. Subsequently, we investigated correlations between the shape and size of ceria nanostructures and the mechanical performance of composites. The samples were character- ized by transmission electron microscopy, scanning electron microscopy, and X-ray diffraction. Compared with commercial ceria filled composites, the composites made with morphology-controlled ceria nanos- tructures show a higher impact strength. It is found that epoxy resins made with high-aspect-ratio ceria nanorods show the highest impact strength, up to 17.27 kJ/m2, which is about four times that of the neat epoxy resin.

Optical constants and their dispersion of Ag-MgF_2 nanoparticle composite films

Ag-MgF_2 composite films with different Ag fractions were prepared through a co-evaporation method. Microstructure analysis shows that the films are composed of amorphous MgF_2 matrix and embedded fcc-Ag nanoparticles. The optical constants and their dispersion of the films, within the wavelength range of 250 - 650 nm, were measured by reflecting spectroscopic ellipsometry. The maximum of the imaginary part ε~″ of the complex dielectric permittivity attributing to the surface plasmon resonance polarization of the Ag nanoparticles in an Ag-MgF_2 film, and the tangent of the phase-shift angle δ resulting from the dielectric loss of the film, occur at λ= 435 nm and λ= 420 nm, respectively. Based on Maxwell-Garnett effective medium theory, the experimentally observed dispersion spectra were reasonably described.

On-Chip Fabrication of Carbon Nanoparticle–Chitosan Composite Membrane

The on-chip fabrication of a carbon nanoparticle-chitosan composite membrane （i.e. a sorbent membrane or a mixed matrix membrane） using laminar flow-based interfacial deprotonation technology was presented in this paper. In addition, the effects of carbon nanoparticles and reactant flow rates on membrane formation were investigated. Finally, the permeability and adsorption capacities of the membrane were discussed. During fabrication, an acidic chitosan solution and a basic buffer solution that contained carbon nanoparticles were introduced into a microchannel. At the flow interface, a freestanding composite membrane with embedded carbon nanoparticles was formed due to the deprotonation of the chitosan molecules. The membrane growth gradually stopped with time from upstream to downstream and the thickness of the membrane increased rapidly and then slowly along the reactant flow direction. The formation of the membrane was divided into two stages. The average growth rate in the first stage was significantly larger than the average growth rate in the second stage. Carbon nanoparticles in the basic solution acted as nucleating agents and made the membrane formation much easier. As the flow rate of the chitosan solution increased, the averaged membrane thickness and the membrane hydraulic permeability initially increased and then decreased. Because of the addition of carbon nanoparticles, the formed membrane had adsorption abilities. The carbon nanoparticle-chitosan composite membrane that was fabricated in this study could be employed for simultaneous adsorption and dialysis in microdevices in the future.

Preparation of Polystyrene/Fe3O4 Nanoparticles in Triton X-100/ Sodium Dodecyl Benzenesulfonate Mixed Surfactant System

The composite nanoparticles of polystyrene/Fe3O4 with a shell-core structure were prepared in the mixed system of Triton X-100 and SDBS. The shell of the composite nanoparticles was formed by polystyrene and the core by Fe3O4 nanoparticles. The diameter of Fe3O4 nanoparticles is about 10 nm and that of the composite nanoparticles 25-35 nm. The XRD spectra and FTIR spectra show that the enwrapping of polystyrene with Fe3O4 nanoparticles was successful.