Stability of fine water droplet clouds

The rate of evaporation of monodisperse water droplets was first evaluated by solving numerically the modified Maxwell equation, assuming the cellular model for a droplet clouds. The results are discussed in comparison with those for a single isolated droplet, which can be obtained analytically. The critical conditions for the droplet cloud to be stable are then evaluated as a function of droplet number concentration, droplet size and initial conditions of the surrounding air. Secondly, the equilibrated system, where a water droplet cloud is steadily mixed with unsaturated air, was analysed on the basis of enthalpy and material balance of the system to evaluate the total volume change of the droplets. Some of these analyses were verified by experiment, using an ultramicroscopic technique which is useful for droplet size analysis.     

Characterization of silica-coated silver nanoparticles prepared by a reverse micelle and hydrolysis–condensation process

Described herein is the synthesis of individually silica-coated silver nanoparticles using a reverse micelle method followed by hydrolysis and condensation of tetraethoxysilane (TEOS). The size of a silica-coated silver nanoparticle can be controlled by changing the reaction time and the concentration of TEOS. By maintaining the size of a silver nanoparticle as a core particle at around 7 nm, the size of a silica-coated silver nanoparticle increased from 13 to 28 nm as the reaction time increased from 1 to 9 h due to an increase in silica thickness. The size of silica-coated silver nanoparticles also increased from 15 to 22 nm as the TEOS concentration increased from 7.8 to 40 mM. The size of a silica-coated silver nanoparticle can be accurately predicted using the rate of the hydrolysis reaction for TEOS. Neither the dispersion nor the film of silica-coated silver nanoparticles exhibited any peak shifting during surface plasmon resonance (SPR) at around 410 nm, whereas, without silica coating, the SPR peak of Ag film shifted to 466 nm.     

Enhancement of the thermal stability and mechanical properties of a PMMA/aluminum trihydroxide composite synthesized via bead milling

The use of aluminum trihydroxide (ATH) fillers as non-halogen flame retardants for polymethylmethacrylates (PMMA) creates a conflict between the mechanical properties and heat resistance of the composites. Therefore, to ensure that the PMMA mechanical properties remain satisfactory, improvements in both the filler–polymer interactions and the ability to control the size and size distribution, morphology and dispersion of the fillers are required. Thus, in the present study, bead milling was used to control both the size distribution and dispersion of ATH fillers in MMA, which had an initial average size of 0.75 μm. The dispersion was obtained by alteration of the surface characteristics of ATH fillers using a silane-based dispersing agent, (3-acryloxypropyl) trimethoxysilane (APTMS). Bead milling successfully comminuted the ATH particles and prevented the formation of ATH agglomerates. The smallest average size of the ATH particles after bead milling was 300 nm. Highly dispersed ATH filler particles were observed in the TEM images of the PMMA/ATH composites. The filler–polymer interaction, i.e. the interaction parameter (B), was calculated. The effects of volume fraction, particle size distribution, and surface modification of the fillers on the results of dynamic mechanical analysis (DMA) are discussed. The thermal stability of the PMMA/ATH composites was also investigated using thermal gravimetric analysis (TGA).     

Giant electric double-layer capacitance of heavily boron-doped diamond electrode

The physical and electrochemical properties of boron-doped polycrystalline diamond electrodes, prepared with various B/C ratio, i.e., 0.1%, 0.5% (BDD-A), 1% (BDD-B), and 5% (BDD-C), were investigated. Electrochemical measurements of the heavily boron-doped films (BDD-C) showed giant electric double-layer capacitance and activity which is significantly larger than BDD-A and BDD-B as well as glassy carbon electrodes. However, interestingly, actual boron concentration of BDD-C was observed to be almost the same as that of BDD-B by secondary ion mass spectroscopy (SIMS) and glow discharge optical emission spectroscopy (GDOES) analysis. It is suggested that the large capacitance is due to a few sp²-bonded carbon impurities, which was observed only in BDD-C, although the amount of the sp²-bonded nondiamond species are very small. In the present work, the reason for the interesting electrochemical properties of heavily boron-doped diamond electrodes is discussed. Furthermore, dimensional stability of the electrodes was also confirmed by conducting harsh anodic treatment.     

Estrogen Stimulates Proliferation and Differentiation of Neural Stem/Progenitor Cells through Different Signal Transduction Pathways

Our previous study indicated that both 17β-estradiol (E2), known to be an endogenous estrogen, and bisphenol A (BPA), known to be a xenoestrogen, could positively influence the proliferation or differentiation of neural stem/progenitor cells (NS/PCs). The aim of the present study was to identify the signal transduction pathways for estrogenic activities promoting proliferation and differentiation of NS/PCs via well known nuclear estrogen receptors (ERs) or putative membrane-associated ERs. NS/PCs were cultured from the telencephalon of 15-day-old rat embryos. In order to confirm the involvement of nuclear ERs for estrogenic activities, their specific antagonist, ICI-182,780, was used. The presence of putative membrane-associated ER was functionally examined as to whether E2 can activate rapid intracellular signaling mechanism. In order to confirm the involvement of membrane-associated ERs for estrogenic activities, a cell-impermeable E2, bovine serum albumin-conjugated E2 (E2-BSA) was used. We showed that E2 could rapidly activate extracellular signal-regulated kinases 1/2 (ERK 1/2), which was not inhibited by ICI-182,780. ICI-182,780 abrogated the stimulatory effect of these estrogens (E2 and BPA) on the proliferation of NS/PCs, but not their effect on the differentiation of the NS/PCs into oligodendroglia. Furthermore, E2-BSA mimicked the activity of differentiation from NS/PCs into oligodendroglia, but not the activity of proliferation. Our study suggests that (1) the estrogen induced proliferation of NS/PCs is mediated via nuclear ERs; (2) the oligodendroglial generation from NS/PCs is likely to be stimulated via putative membrane-associated ERs.     

High luminance YAG:Ce nanoparticles fabricated from urea added aqueous precursor by flame process

High luminance Y₃Al₅O₁₂:Ce³⁺ (YAG:Ce) nanoparticles were prepared from urea-added nitrate aqueous precursor by flame-assisted spray pyrolysis (FASP). The addition of urea into nitrate precursor plays an important role in YAG:Ce nanoparticle formation and in improving its optical performance. The decomposition and combustion of urea in the flame zone provides additional heat to the particles, which coupled with the evolution of large volumes of gasses, contributes to nanoparticle formation. The as-prepared nanoparticles are hexagonal YAlO₃, that are nearly spherical, rough on the surface and dense—and they can be converted to YAG:Ce after being annealed at 1200 °C for 4 h. The heat-treated particles are single crystalline, smooth in surface and dense with an average size around 50 nm. The optimum cerium-doping concentration of YAG:Ce nanoparticles is 4.0 at.%, which exhibits quantum efficiency of 45.0%. This quantum efficiency is comparable with that of YAG:Ce nanoparticles produced from other processes. The efficient emission of YAG:Ce nanoparticles also originates from a relatively good distribution of Ce ions incorporated into the host material of YAG as evidenced from the elemental mapping analysis.     

A Pulse Combustion-Spray Pyrolysis Process for the Preparation of Nano- and Submicrometer-Sized Oxide Particles

The preparation of nano- and submicrometer particles using an integrated pulse combustion–spray pyrolysis process was investigated for the first time. Zinc oxide nanoparticles with average sizes ranging from 20 to 40 nm were synthesized using a salt precursor with a lower decomposition temperature than the pulse combustion (PC) temperature. Particles of a doped-type oxide, gadolinium oxide-doped with europium, were also produced from a precursor, whose decomposition temperature was higher than the PC temperature, and were observed to be ellipsoidal–toroidal in shape and submicrometer in size. The high-intensity fluctuating pressures generated by PC and the precursor decomposition temperature are proposed as the reasons for the formation of either nanoparticles or aspherical particles. In addition, hot gas fluctuating flow in PC enhanced energy transfer, resulting in more crystalline particles, as compared with particles produced by conventional spray pyrolysis.     

Production of Narrow‐Size‐Distribution Polymer‐Pigment‐Nanoparticle Composites via Electrohydrodynamic Atomization

Near‐monodisperse, size‐controllable, poly(methyl methacrylate)‐pigment nanoparticle composites were produced using electrohydrodynamic atomization (EHDA). The geometric mean diameters of the composite particles were in the 0.91 to 1.90 µm‐diameter range with geometric standard deviations of approximately 1.05 to 1.12. Increasing the polymer volume fraction and liquid flow‐rate resulted in an increase in the diameter of the composite particles, which agreed well with droplet scaling relations for EHDA. The results here demonstrate that EHDA can be used for polymer‐nanoparticle‐composite production and as an alternative to conventional inkjet printing.

     

Preparation of Copper-Ruby Glasses by Sputtering: The Effect of Atmosphere on the Growth of Copper Particles

Copper-ruby glasses were prepared by the sputtering method and the effect of reducing treatment was examined. The reducing was carried out either during sputtering or heat treatment. Optical absorption was related to the growth of copper particles. The results are summarized as follows: (i) the volume fraction of copper particles in the glasses which are heat-treated in air increases with the addition of hydrogen in the sputtering gas. (ii) The copper particles do not grow larger than 8 nm by heat treatment in reducing atmosphere, whereas they grow as large as 12 nm in air. (iii) Reducing during heat treatment gives a pronounced effect only when sputtering was not carried out under reducing conditions. The origin of these phenomena was also discussed, considering the mechanism of nucleation and growth of copper particles.