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991.
Peng Jiang Jian-Jun Zhou Rui Li Yan Gao Tao-Lei Sun Xiao-Wei Zhao Yan-Juan Xiang Si-Shen Xie 《Journal of nanoparticle research》2006,8(6):927-934
PVP (poly(vinyl pyrrolidone))-capped micrometer-sized twinned gold (Au) plates with the shape of hexagon or triangle have been successfully synthesized in a large quantity by reducing hydrogen tetrachloroauric acid (HAuCl4·3H2O) using ethylene glycol in the presence of (PVP) molecules at 200°C under the extra condition of autogenous pressure. Clear twin boundaries in thus-obtained Au plates have been observed by scanning electron microscope (SEM). To further elucidate the mechanism of formation of the twinned Au plates, transmission electron microscopy (TEM) has been employed to characterize smaller Au nanoplates obtained simultaneously with the Au microplates, the occurrence of 1/3{422} forbidden reflections in selected area electron diffraction (SAED) can be believed to result from the presence of twinning boundary within the Au (111) plane normal to TEM electron beam. In addition, X-ray photoelectron spectroscopy (XPS) experiment has confirmed that PVP molecules exist on the surface of the Au cores, which may play a very important role in the formation and evolution of the twinned Au plates. A possible growth mechanism has been suggested to explain the Au plate evolution from nanometer to micrometer. 相似文献
992.
Philipp Reissaus Tomas Waldemarsson Jürgen Blum Dominik Clément Isabel Llamas Harald Mutschke Frank Giovane 《Journal of nanoparticle research》2006,8(5):693-703
In order to find reliable collector surfaces for the Mesospheric Aerosol – Genesis, Interaction and Composition (MAGIC) sounding rocket experiment, intended to collect atmospheric nanoparticles, the sticking efficiency of nanoparticles was measured on several targets of different materials. The nanoparticles were generated by a molecular beam apparatus in Jena, Germany, by laser ablation (Al2O3 particles, diameter 5–50 nm) and by laser pyrolysis (carbon particles, diameter 10–20 nm). In a vacuum environment (>10−5 mbar) the particles condensed from the gas phase, formed a particle beam, and were accelerated to ∼
∼1 km/s. The sticking efficiency on the target materials carbon, gold and grease was measured by a microbalance. Results demonstrate moderate to high sticking probabilities. Thus, the capture and retrieval of atmospheric nanoparticles was found to be quantitatively feasible. 相似文献
993.
Hong-liang Li 《Journal of solid state chemistry》2003,172(1):102-110
Hexagonal CdSe and hexagonal CdS nanoparticles have been prepared using Cd(Ac)2 and less hazardous elemental Se or S as precursors, respectively, with the aid of ultrasound irradiation under an atmosphere of H2/Ar (5/95, V/V). The products consist of 7-10 nm nanocrystallites which aggregated in the form of polydispersive nanoclusters with sizes in the range 30-40 nm in the case of CdSe, and near monodispersive nanoclusters with a mean size of about 40 nm in the case of CdS. X-ray diffraction, high-resolution TEM and SAED patterns (selected area electron diffraction patterns) show that the as-prepared particles are well crystallized. X-ray photoelectron spectroscopy (XPS) measurements further confirm the formation of CdSe and CdS. Diffuse reflection spectra indicate that both the CdSe and the CdS nanocryslallites are direct band-gap semiconductors with band-gap values of about 1.83 and 2.62 eV, respectively. Control experiments demonstrate that the hydrogen is the reducing agent, and the extreme high temperature induced by the collapse of the bubble accelerates the reduction of elemental Se or S by hydrogen. An ultrasound assisted in situ reduction/combination mechanism is proposed. 相似文献
994.
Cross-sectional observation of the oxide scale formed by oxidation of TiC single crystals with (100), (110) and (111) faces at 1500 °C for 30 min in a mixed gas of Ar/O2 (PO2=0.08 kPa) was performed by transmission electron microscope (TEM). The oxide scale was composed of outer (zone 2) and inner (zone 1) subscales. TEM and selected area electron diffraction combined with X-ray energy dispersion analysis showed that the zone 2 consists of rutile and pores and the zone 1 of carbon and titanium oxide, identified as Ti3O5 in the oxide scale formed on the (110) face. Zone 1 formed on the (100) and (111) faces showed crisscross patterns, in contrast to the (110) with the wavy lamellar pattern. 相似文献
995.
用气体中蒸发的方法在蓝宝石基片上制备了纳米InSb颗粒膜.通过透射电镜分析显示,该方法可以制得多晶的InSb纳米颗粒,且颗粒均匀地分布在蓝宝石基片表面上;用X射线能谱仪分析样品得到两种元素的百分比接近1:1.实验结果表明,通过改变设备的工作条件,可以得到具有不同颗粒尺寸的InSb纳米颗粒. 相似文献
996.
997.
Nano-sized polyacrylonitrile (PAN) particles were prepared under the catalytic effect of in situ developed CoCl2/EDTA complex with ammonium persulfate as the initiator in the absence of any added emulsifier. The emulsion polymerization was studied at varying concentrations of the initiator, monomer, complex and solvent over a temperature range of 30-70℃. The overall activation energy (Ea, 49.79 kJ/mol), energy of dissociation of initiator (Ed,82.68 kJ/mol), number of micelles (0.163×1018) and the viscosity average molecular weight of the polymer were computed. The distribution of particle sizes was determined by transmission electron microscopy (TEM). It was found that the oil-in-water polymerization was stabilized by the presence of the CoCl2/EDTA in situ complex reducing the particle size into the nano order. The average diameters of PAN nano particles, obtained by TEM, were in the range of 50-150 nm at the maximum conversion. The experimental particle size was mainly dependent on the concentration of the complex and temperature. 相似文献
998.
Yao‐Te Chang Ching‐Fong Shu Chyi‐Ming Leu Kung‐Hwa Wei 《Journal of polymer science. Part A, Polymer chemistry》2003,41(23):3726-3735
We synthesized an AB2‐type monomer, 4‐{4‐[di(4‐aminophenyl)methyl]phenoxy}phthalic acid, which contained one phthalic acid group and two aminophenyl functionalities. The direct self‐polycondensation of the AB2‐type monomer in the presence of triphenylphosphite as an activator afforded a hyperbranched poly(ether imide) with a large number of terminal amino groups. This polymer was characterized with 1H NMR and IR spectroscopy. The degree of branching of the hyperbranched poly(ether imide) was approximately 56%, as determined by a combination of model compound studies and an analysis of 1H NMR spectroscopy integration data. The terminal amino groups underwent functionalization readily. The solubility and thermal properties of the resulting polymers depended on the nature of the chain end groups. In addition, the hyperbranched poly(ether imide) was grafted with polyhedral oligomeric silsesquioxane (POSS). Transmission electron microscopy analysis revealed that the grafted POSS molecules aggregated to form a nanocomposite material. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 3726–3735, 2003 相似文献
999.
ChangGangHU HuiXIE GanZuoL YaAN ZhongNiWANG XiaoYiZHANG JingPingTIAN 《中国化学快报》2005,16(5):681-684
The spontaneous formation of vesicles in the aqueous of cationic surfactant phosphate (PTA) and anionic surfactant sodium dodecyl sulfate (SDS) at certain mixing ratios have obtained^1. The addition of urea or Nal will expand the range of spontaneous vesicle formation. The fact is demonstrated by negative-staining transmission electron microscope(TEM) and dynamic light scattering(DLS) methods. The phenomenon especially in the part of urea is reported by us at first. Mechanism of urea/Nal-induced vesicles formation is discussed from the viewpoint of the molecular geometry packing parameter f, conformation and interaction. 相似文献
1000.
Exfoliated polyamide‐6 (PA6)/organoclay nanocomposite films with planar‐oriented clay platelets were prepared by the simple hot pressing of melt‐extruded nanocomposite pellets. The average distance between the neighboring clay platelets was controlled by changes in the clay loading content in the nanocomposites. The effects of the clay platelet spacing on the crystallization behavior of PA6 were investigated with transmission electron microscopy and wide‐angle X‐ray diffraction. The crystal lamellae were found to be mainly perpendicular to the clay surface for the nanocomposites with large spacing between the clay sheets at low clay loading contents. This perpendicular orientation morphology was attributed to the strong interactions between the PA6 molecular chain and the clay surface. In contrast, the crystal lamellae were found to be parallel to the clay surface when the spacing between the neighboring clay platelets was less than 30 nm. It was concluded that the confinement crystallization of PA6 within the nanoscale channels formed by clay sheets resulted in this parallel orientation texture. © 2005 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 284–290, 2006 相似文献