纳米导电微粒子材料

大连三科科技发展有限公司生产的纳米导电微粒子材料涂敷于显示管、彩色显像管及玻璃镀层上,具有防眩光、静电、辐射等功能,还可减轻红、紫外线的照射,提高图像清晰度,减轻辐射危害,可广泛应用于显示器件,触摸屏制造的电子工业领域,微波炉。

高钒高速钢中碳化钒的微细结构分析

利用扫描电镜、透射电镜和X射线能量分散谱仪对高钒高速钢中合金碳化物———碳化钒的精细结构及微区成分进行分析。结果发现:碳化钒中由于碳的有序缺位形成了V6C5简单六方超点阵结构;碳化钒内有大量纳米微粒子存在;微粒子处Cr、Mo和Fe元素含量较高,尤其是Mo元素,可高达20%(质量分数)以上。

Synthesis,characterization and photocatalytic performance of rod-shaped Pt/PbWO_4 composite microcrystals

Rod-shaped PbW O4 microcrystals of length 1 μm were fabricated by a hydrothermal route and subsequent calcination. Pt nanoparticles（NPs） of different contents（0.5 wt%,1 wt% and 2 wt%） were subsequently deposited on the PbW O4 microcrystals,producing robust Pt/PbW O4 composite microcrystals. The PbW O4 microcrystals and Pt/PbW O4 photocatalysts were characterized by X-ray diffraction,N2 sorption measurements,scanning electron microscopy,transmission electron microscopy,and X-ray photoelectron,photoluminescence,Fourier-transform infrared,and ultraviolet-visible diffuse reflectance spectroscopies. The photocatalytic performances of the catalysts were evaluated by the consecutive photocatalytic degradation of acid orange II dye. The Pt/PbW O4 composite microcrystals exhibited high photocatalytic activity and stability. The deposition of Pt NPs produced surface plasmon resonance（SPR）,which induced a large visible light absorption. A Pt NP content of 1-2 wt% resulted in an ~2 times increase in photocatalytic activity,compared with the activity of Pt/PbW O4. The crystal structure and high crystallinity of PbW O4 resulted in its favorable photocatalytic property,and the SPR effect of the Pt NPs promoted visible light harvesting. The Pt NPs also enhanced the separation of photo-generated electrons and holes,which further promoted the photocatalytic reaction.

Pd micro-nanoparticles electrodeposited on graphene/polyimide membrane for electrocatalytic oxidation of formic acid

A novel Pd electrocatalyst with flowerlike micro-nanostructures was synthesized by electrochemical deposition on a flexible graphene/polyimide（Gr/PI） composite membrane and characterized by scanning electron microscopy（SEM）,X-ray diffraction（XRD）.The Pd micro-nanoparticles were prepared on a COOH-CNTs/PI membrane as a comparative sample.The XRD and SEM investigations for Pd electrodeposition demonstrate that the particle size of Gr/PI composite membrane is smaller than that of COOH-CNTs/PI membrane,while the uniform and dense distribution of Pd micro-nanoparticles on the Gr/PI composite membrane is greater than that on the COOH-CNTs/PI membrane.The electrocatalytic properties of Pd/Gr/PI and Pd/COOH-CNTs/PI catalysts for the oxidation of formic acid were investigated by cyclic voltammetry（CV） and chronoamperometry（CA）.It is found that the electrocatalytic activity and stability of Pd/Gr/PI are superior to those of Pd/COOH-CNTs/PI catalyst.This is because smaller metal particles and higher dense distribution desirably provide abundant catalytic sites and mean higher catalytic activity.Therefore,the Pd/Gr/PI catalyst has better catalytic performance for formic acid oxidation than the Pd/COOH-CNTs/PI catalyst.

Structure and magnetic properties of Cu-Ni alloy nanoparticles prepared by rapid microwave combustion method

Cu-Ni alloy nanoparticles were prepared by a microwave combustion method with the molar ratios of CU2＋ to Ni2＋ as 3：7, 4：6, 5：5, 6：4 and 7：3. The as-prepared samples were characterized by XRD, HR-SEM, EDX and VSM. XRD and EDX analyses suggest the formation of pure alloy powders. The average crystallite sizes were found to be in the range of 21.56-33.25 nm. HR-SEM images show the clustered/agglomerated particle-like morphology structure. VSM results reveal that for low Ni content （CusNis, Cu6Ni4 and Cu7Ni3）, the system shows paramagnetic behaviors, whereas for high Ni content （Cu3Ni7 and Cu4Ni6）, it becomes ferromagnetic.

Carbon-supported ultrafine Pt nanoparticles modified with trace amounts of cobalt as enhanced oxygen reduction reaction catalysts for proton exchange membrane fuel cells

To accelerate the kinetics of the oxygen reduction reaction(ORR)in proton exchange membrane fuel cells,ultrafine Pt nanoparticles modified with trace amounts of cobalt were fabricated and decorated on carbon black through a strategy involving modified glycol reduction and chemical etching.The obtained Pt36Co/C catalyst exhibits a much larger electrochemical surface area(ECSA)and an improved ORR electrocatalytic activity compared to commercial Pt/C.Moreover,an electrode prepared with Pt36Co/C was further evaluated under H2-air single cell test conditions,and exhibited a maximum specific power density of 10.27 W mgPt^-1,which is 1.61 times higher than that of a conventional Pt/C electrode and also competitive with most state-of-the-art Pt-based architectures.In addition,the changes in ECSA,power density,and reacting resistance during the accelerated degradation process further demonstrate the enhanced durability of the Pt36Co/C electrode.The superior performance observed in this work can be attributed to the synergy between the ultrasmall size and homogeneous distribution of catalyst nanoparticles,bimetallic ligand and electronic effects,and the dissolution of unstable Co with the rearrangement of surface structure brought about by acid etching.Furthermore,the accessible raw materials and simplified operating procedures involved in the fabrication process would result in great cost-effectiveness for practical applications of PEMFCs.

Microstructure and properties of Al-doped ODS steels prepared by wet-milling and SPS methods

In this paper,15Cr-ODS steels containing 0,1 wt%,2 wt%and 3 wt%Al element were fabricated by combining wet-milling and spark plasma sintering(SPS)methods.The microstructure and mechanical properties of ODS steel were investigated by XRD,SEM,TEM,EBSD and tensile tests.The results demonstrate that the Al addition significantly refines the particle precipitates in the Fe-Cr matrix,leading to the obvious refinement in grain size of matrix and the improvement of mechanical properties.The dispersion particles in ODS steels with Al addition are identified as Al2O3 and Y_(2)Ti_(2)O_(7)nanoparticles,which has a heterogeneous size distribution in the range of 5 nm to 300 nm.Increasing Al addition causes an obvious increase in tensile strength and a decline in elongation.The tensile strength and elongation of 15Cr-ODS steel containing 3 wt%Al are 775.3 MPa and 15.1%,respectively.The existence of Al element improves the corrosion resistance of materials.The ODS steel containing 2 wt%Al shows corrosion potential of 0.39 V and passivation current density of 2.61×10^(−3)A/cm^(2)(1.37 V).This work shows that Al-doped ODS steels prepared by wet-milling and SPS methods have a potential application in structural parts for nuclear system.

Effect of WO3 Nanoparticle Loading on the Microstructural, Mechanical and Corrosion Resistance of Zn Matrix/TiO2-WO3 Nanocomposite Coatings for Marine Application

In this study, for marine application purposes, we evaluated the effect of process parameter and particle loading on the microstructure, mechanical reinforcement and corrosion resistance properties of a Zn-TiO2-WO3 nanocomposite produced via electrodeposition. We characterized the morphological properties of the composite coatings with a Scanning Electron Microscope （SEM） equipped with an Energy Dispersive Spectrometer （EDS）. We carried out mechanical examination using a Dura Scan hardness tester and a CERT UMT-2 multi-functional tribological tester. We evaluated the corrosion properties by linear polarization in 3.5% NaCl. The results show that the coatings exhibited good stability and the quantitative particle loading greatly enhanced the structural and morphological properties, hardness behavior and corrosion resistance of the coatings. We observed the precipitation of this alloy on steel is greatly influenced by the composite characteristics.

Preparation of gold clusters on metal oxides by deposition-precipitation with microwave drying and their catalytic performance for CO and sulfide oxidation

Gold clusters and small nanoparticles supported on metal oxides could be prepared by deposition‐precipitation followed by microwave irradiation as a drying method and then calcination.The drying method influenced the size of the Au particles.Au(III)was partly reduced during conventional oven drying,resulting in Au aggregates.In contrast,Au(III)was preserved during microwave drying owing to rapid and uniform heating,and the Au diameter was minimized to1.4nm on Al2O3.This method can be applied to several metal oxide supports having different microwave absorption efficiencies,such as MnO2,Al2O3,and TiO2.These catalysts exhibited higher catalytic activities for CO oxidation at low temperature and for selective aerobic oxidation of sulfide than those prepared by conventional methods.

Irradiation Damage of Nano-C2S Particles Studied by In-Situ Transmission Electron Microscopy

Development of a reactive nanocement is a new approach to improve the physical and chemical properties of construction materials. However, due to the decreased size of cement particles, beam damage during transmission electron microscope （TEM） observation becomes more severe than in conventional cement. In this work, irradiation damage to nano-C2S （dicalcium silicate） is observed and studied by in-situ evolution of diffraction patterns （DP）, high resolution TEM （HRTEM）, and electron energy-loss spectroscopy （EELS）. The results show that the damage to nano-C2S occurs through a decomposition reaction. Nano-C2S is first amorphized, and then re-crystallized into CaO nano-crystals with average size of 7 nm surrounded by an amorphous matrix of Si and SiO2. During this process, C2S particles exhibit volume shrinkage. The damage energy causing the reaction was analyzed and electron-electron inelastic scattering produced radiolysis and heat, leading to the observed phenomena.

Synthesis and Optical Properties of ZnO Nanoparticles in Submicron PS Hollow Reactors

ZnO nanoparticles were first encapsulated in submicron PS hollow microspheres through two-step swelling process of core-shell structured PMMA/PS （PMMA： polymethyl methao- rylate） microspheres in acid-alkali solution, and the ZnO precursors, i.e. the ethanol solu- tions of （CHaCOO）2Zn and LiOH. The transmission electron microscope, X-ray diffraction, and thermogravimetric analysis results show that the feeding order of ethanol solutions of （CH3COO）2Zn and LiOH in the second swelling step has great influence on the loading efficiency and the size of ZnO nanoparticles, but little on their crystal form. The photolumi- nescence and UV-Vis absorption behavior of ZnO/PS microspheres show that the PS shell can effectively avoid the fluorescence quenching effect.

Antibacterial Properties of Novel Bacterial Cellulose Nanofiber Containing Silver Nanoparticles

In this work,we describe a novel facile method to prepare long one-dimensional hybrid nanofibers by using hydrated bacterial cellulose nanofibers(BCF)as a template.Silver(Ag)nanoparticles with an average diameter of 1.5 nm were well dispersed on BCF via a simple in situ chemical-reduction between AgNO3and NaBH4at a relatively low temperature.A growth mechanism is proposed that Ag nanoparticles are uniformly anchored onto BCF by coordination with BC-containing hydroxyl groups.The bare BCF and as-prepared Ag/BCF hybrid nanofibers were characterized by several techniques including transmission electron microscopy,X-ray diffraction,thermogravimetric analyses,and ultraviolet-visible(UV-Vis)absorption spectra.The antibacterial properties of Ag/BCF hybrid nanofibers against Escherichia coli(E.coli,Gram-negative)and Staphylococcu saureus(S.saureus,Gram-positive)bacteria were evaluated by using modified Kirby Bauer method and colony forming count method.The results show that Ag nanoparticles are well dispersed on BCF surface via in situ chemical-reduction.The Ag/BCF hybrid nanofiber presents strong antibacterial property and thus offers its candidature for use as functional antimicrobial agents.

Suppression of gold nanoparticle agglomeration and its separation via nylon membranes

Use of ultraporous nylon membrane is one of the most widely employed techniques for removal of hard and soft nanoparticles in the semiconductor industry, and the accurate determination of membrane pore size is necessary in order to avoid manufacturing defects caused by contamination. The gold nanoparticle has several benefits for the evaluation of polymeric membranes; however, the nanoparticles agglomerate easily on the nylon membrane and make it difficult to evaluate the membrane precisely. The properties of 2-amino-2-hydroxymethyl-1,3-propanediol(ADP) ligand in gold nanoparticle solution were systematically investigated, and ADP was utilized for improved evaluation of the nylon membranes. Nylon membrane used in this study was prepared by phase inversion techniques. Ultrathin dense layer on top of the membrane surface and Darcy structures in the microporous membrane support were observed. The gold particle rejection was carried out at various p H values from 4 to14 and higher rejection was observed at p H 4 and 8. The suppression of gold colloid agglomeration using ADP and monodispersity of gold colloids was also analyzed by confocal laser scanning microscopy(CLSM), transmission electron microscopy(TEM), and scanning electron microscopy(SEM). van der Waals interaction energy of the particles was reduced in the addition of ADP. The presence of ADP ligand in the gold solutions prevented the agglomeration of gold nanoparticles and reduced the adsorption of the particles on the nylon membrane surface,leading to precise evaluation of membrane pore sizes.

ZrO2/PMMA Nanocomposites： Preparation and Its Dispersion in Polymer Matrix

ZrO2/PMMA nanocomposite particles are synthesized through an in-situ free radical emulsion polymerization based on the silane coupling agent （Z-6030） modified ZrO2 nanoparticles, and the morphology, size and its distribution of nanocomposite particles are investigated. Scanning electron microscopy （SEM） images demonstrate that the methyl methacrylate （MMA） feeding rate has a significant effect on the particle size and morphology. When the MMA feeding rate decreases from 0.42 ml-min-1 to 0.08 ml. min-1, large particles （about 200-550.nm） will not form, and the size distribution become narrow （36-54 nm）. The average nanocomposite particles size increases from 34 nm to 55 nm, as the MMA/ZrO2 nanoparticles mass ratio increased from 4 ： 1 to 16 ： 1. Regular spherical ZrO2/PMMA nanocomposite particles are synthesized when the emulsifier OP-10 concentration is 2 mg.m1-1. The nanocomposite particles could be mixed with VAc-VeoVa10 polymer matrix just by magnetic stirring to prepare the ZrOE/PMMA/VAc-VeoVal0 hybrid coatings. SEM and atomic force microscopy （AFM） photos reveal that the distribution of the ZrO2/PMMA nanocomposite particles in the VAc-VeoVal0 polymer matrix is homogenous and stable. Here, the grafted-PMMA polymer on ZrO2 nanoparticles plays as a bridge which effectively connects the ZrO2 nanoparticles and the VAc-VeoVal0 polymer matrix with improved comparability. In consequence, the hybrid coating with good dispersion stability is obtained.

Synthesis and Characterization of MgSb2O6 Trirutile-Type in Low Presence Concentrations of Ethylenediamine

The nanoparticles MgSb206 with trirutile-type structure were prepared by colloidal method using ethylanediamine （0.5 and 0.75 mL）, following a calcination at 800 ℃. After, those powders were analyzed by x-ray obtaining a tetragonal structure with cell parameters, a = 4.64 A and c = 9.25 A and special group P42/mnm. Using a scanning electron microscopy were analyzed the powders calcined at 800 ℃, showing the formation of micro-plates, micro-rods, nanoparticles and morphology as rice grains. Employing a transmission electron microscopy, were found nanostructures hexagonal shaped with sizes of- 33.6 nm （0.5 mL） and 28.6 nm （0.75 mL）.

Facile Fabrication of Platinum Nanoparticles Supported on Nitrogen-doped Carbon Nanotubes and Their Catalytic Activity

A facile impregnation method under mild condition is designed for synthesis of highly dispersed Pt nanoparticles with a narrow size of 4-7 nm on nitrogen-doped carbon nanotubes （CNx）. CNx do not need any pre-surface modification due to the inherent chemical activity. The structure and nature of Pt/CNx were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and energy dispersive spectroscopy spectrum. All the experimental results revealed that the large amount of doped nitrogen atoms in CNx was virtually effective for capturing the Pt（IV） ions. The improved surface nitrogen functionalities and hydrophilicity contributed to the good dispersion and immobi- lization of Pt nanoparticles on the CNx surface. The Pt/CNx served as active and reusable catalysts in the hydrogenation of allyl alcohol. This could be attributed to high dispersion of Pt nanoparticles and stronger interaction between Pt and the supports, which prevented the Pt nanoparticles from aggregating into less active Pt black and from leaching as well.

High densities of magnetic nanoparticles supported on graphene fabricated by atomic layer deposition and their use as efficient synergistic microwave absorbers

An atomic layer deposition （ALD） method has been employed to synthesize Fe3O4/graphene and Ni/graphene composites. The structure and microwave absorbing properties of the as-prepared composites are investigated. The surfaces of graphene are densely covered by Fe3O4 or Ni nanoparticles with a narrow size distribution, and the magnetic nanoparticles are well distributed on each graphene sheet without significant conglomeration or large vacancies. The coated graphene materials exhibit remarkably improved electromagnetic （EM） absorption properties compared to the pristine graphene. The optimal reflection loss （RL） reaches -46.4 dB at 15.6 GHz with a thickness of only 1.4 mm for the Fe3O4/graphene composites obtained by applying 100 cycles of Fe2O3 deposition followed by a hydrogen reduction. The enhanced absorption ability arises from the effective impedance matching, multiple interfacial polarization and increased magnetic loss from the added magnetic constituents. Moreover, compared with other recently reported materials, the composites have a lower filling ratio and smaller coating thickness resulting in significantly increased EM absorption properties. This demonstrates that nanoscale surface modification of magnetic particles on graphene by ALD is a very promising way to design lightweight and high-efficiency microwave absorbers.

Convective Assembly of Linear Gold Nanoparticle Arrays at the Micron Scale for Surface Enhanced Raman Scattering

A convective assembly technique at the micron scale analogous to the writing action of a ＂pipette pen＂ has been developed for the linear assembly of gold nanoparticle strips with micron scale width and millimeter scale length for surface enhanced Raman scattering （SERS）. The arrays with interparticle gaps smaller than 3 nm are hexagonally stacked in the vicinity of the pipette tip. Variable numbers of stacked layers and clean surfaces of the assembled nanoparticles are obtained by optimizing the velocity of the pipette tip. The SERS properties of tile assembled nanoparticle arrays rely on their stacking number and surface cleanliness.

Recent progress in the application of microfluidic systems and gold nanoparticles in immunoassays

Immunoassays are useful for many bioassays. Many new techniques and materials are introduced into the immunoassay to improve the efficiency. This paper reviews recent progress in the application of microfluidic systems and gold nanoparticles in immunoassay. The micro/nano technologies and materials can offer good sensitivity, fast detection, cost-effectiveness and easy signal readout. In particular, the miniaturization of microfluidics and colorimetric assays based on gold nanoparticles have dramatically improved the efficiency of immunoassays.

Effects of Al_2O_3 nanoparticles on properties of self compacting concrete with ground granulated blast furnace slag (GGBFS) as binder

In this work, strength assessments and percentage of water absorption of self compacting concrete containing ground granulated blast furnace slag （GGBFS） and A1203 nanoparticles as binder have been investigated. Portland cement was replaced by different amounts of GGBFS and the properties of concrete specimens were investigated. Although it negatively impacts the physical and mechanical properties of concrete at early ages of curing, GGBFS was found to improve the physical and mechanical properties of concrete up to 45 wt% at later ages. A1203 nanoparticles with the average particle size of 15 nm were added partially to concrete with the optimum content of GGBFS and physical and mechanical properties of the specimens were measured. A1203 nanoparticle as a partial replacement of cement up to 3.0 wt% could accelerate C-S-H gel formation as a result of increased crystalline Ca（OH）2 amount at the early ages and hence increase strength and improve the resistance to water permeability of concrete specimens. The increase of the A1203 nanoparticles＇ content by more than 3.0 wt% would cause the reduction of the strength because of the decreased crystalline Ca（OH）2 content required for C-S-H gel formation. Several empirical relationships have been presented to predict flexural and split tensile strength of the specimens by means of the corresponding compressive strength at a certain age of curing. Accelerated peak appearance in conduction calorimetry tests, more weight loss in thermogravimetric analysis and more rapid appearance of the peaks related to hydrated products in X-ray diffraction results, all indicate that A1203 nanoparticles could improve mechanical and physical properties of the concrete specimens.