Evaluation of glass materials by using the line-focus-beam ultrasonic-material-characterization system

We developed experimental procedures to evaluate glass materials using the line-focus-beam ultrasonic-material-characterization (LFB-UMC) system. We prepared 28 specimens of a commercial borosilicate glass from random lots, and measured the velocities of leaky-surface acoustic waves (LSAWs) and leaky-surface-skimming compressional waves (LSSCWs), VLSAW and VLSSCW, using V(z) curve measurements at 225 MHz and 23 degrees C. The velocities for VLSAW ranged from 3121.83 m/s to 3149.77 m/s, with a maximum deviation of 27.94 m/s. The velocities for VLSSCW ranged from 5547.7 m/s to 5585.0 m/s, with a maximum deviation of 37.3 m/s. To investigate these observed variations in VLSAW and VLSSCW, we measured the bulk acoustic wave (BAW) properties, viz., longitudinal and shear velocities, then the densities and the chemical compositions of 8 of the 28 specimens. The LFB-UMC measurements confirmed that decreases in VLSAW and VLSSCW occur mainly with the B2O3 dopant concentrations, corresponding to the decrease of shear-wave and longitudinal-wave velocities that are caused by the decrease of the stiffness constants c44 and c11, respectively, rather than with decreased densities. The sensitivities are -6.36 x 10(-2) wt%/(m/s) for VLSAW and -4.87 x 10(-2) wt%/(m/s) for VLSSCW. This demonstrates that the LFB-UMC system is effective for evaluating glass materials and controlling production processes, by analyzing variations in chemical composition through the super-accurate velocity measurements of LSAWs and LSSCWs.     

Isolation of hesperidin from peels of thinned Citrus unshiu fruits by microwave-assisted extraction

Simultaneous extraction by microwave-irradiation and crystallisation were performed in the same pot of solvent of 70% (v/v) aqueous ethanol for isolation of hesperidin from thinned immature fruit peels of Citrus unshiu as refining of Citrus waste biomass. The hesperidin content in immature fruits peels was about 3.2-fold higher than that of mature fruit. After microwave-assisted extraction (MAE), the yield of hesperidin reached 58.6 mg/g, which was comparable to the amount obtained after extraction using DMSO:methanol (1:1, v/v) as a solvent for 30 min at room temperature. Heating temperature and time for isolation of hesperidin crystallites were optimised as 140 °C and 8 min by using response surface methodology. Under this optimal condition, 86.8% (47.7 mg/g) of total hesperidin was isolable by MAE and low-temperature storage (5 °C, 24 h).     

CoCl(2) inhibits neural differentiation of retinoic acid-treated embryoid bodies

The effects of CoCl(2) on retinoic acid (RA)-treated embryoid bodies (EBs) were investigated. Four-day EBs were treated with 5x10(-6) M of RA for 4 d, then subjected to attached culturing for 7 d in the presence of CoCl(2) at 0, 20, and 100 microM. Differentiation into MAP2- and GFAP-immunopositive cells was inhibited by CoCl(2) in a dose-dependent manner. Next, RA-treated EBs were dissociated into single cells and cultured for 7 d at an initial cell density of 1x10(3)/cm(2). The number of cells increased in a CoCl(2)-dose dependent fashion. In cultures with 100 microM of CoCl(2), more than 90% of the cells were immunopositive for nestin and nestin-immunopositive cells formed clusters, while there were few cells immunopositive for MAP2 or GFAP. These results suggest that CoCl(2) inhibits neural differentiation of RA-treated EB cells and promotes the proliferation of nestin-immunopositive cells, i.e., embryonic stem (ES)-derived neural stem-like cells.     

Inhibiting Surface Diffusion to Synthesize 3D Bicontinuous Nanoporous N-Doped Carbon for Boosting Oxygen Reduction Reaction in Flexible All-Solid-State Al-Air Batteries

Catalyzing oxygen reduction reaction (ORR) and accelerating oxygen diffusion are two key challenges for the requirements of the cathode catalysts in the metal-air batteries. A promising strategy for improving both ORR performance and mass diffusion simultaneously is to build carbon-based catalysts with ORR-active chemical dopants and 3D interconnected porosity. Herein, a 3D nanoporous N-doped carbon with bicontinuous porosity and interconnected open-pore channels is reported, which is prepared by a polyaniline-assisted template method. The polyaniline can efficiently inhibit the surface diffusion-caused template coarsening, achieving a small pore size of 35 nm. The small porous morphology gives rise to a high N-dopant concentration up to 7.20 at.%, which in turn exhibits a commercial Pt/C-comparable ORR performance together with satisfied durability in alkaline media. Using these nanoporous carbon catalysts as air electrodes, an all-solid-state flexible Al-air battery is assembled with the measured maximum power density reaching 130.5 mW cm⁻², as compared to 106.2 mW cm⁻² when the commercial Pt/C standard is used. This study provides an efficient method to synthesize 3D N-doped carbon with bicontinuous nano-sized pore channels for wide-ranging applications in portable and flexible devices.     

Preparation of micro-dot electrodes of LiCoO2 and Li4Ti5O12 for lithium micro-batteries

Fabrications of micro-dot electrodes of LiCoO₂ and Li₄Ti₅O₁₂ on Au substrates were demonstrated using a sol-gel process combined with a micro-injection technology. A typical size of prepared dots was about 100 μm in diameter, and the dot population on the substrate was 2400 dots cm⁻². The prepared LiCoO₂ and Li₄Ti₅O₁₂ micro-dot electrodes were characterized with scanning electron microscopy, X-ray diffraction, micro-Raman spectroscopy, and cyclic voltammetry. The prepared LiCoO₂ and Li₄Ti₅O₁₂ micro-dot electrodes were evaluated in an organic electrolyte as cathode and anode for lithium micro-battery, respectively. The LiCoO₂ micro-dot electrode exhibited reversible electrochemical behavior in a potential range from 3.8 to 4.2 V versus Li/Li⁺, and the Li₄Ti₅O₁₂ micro-dot electrode showed sharp redox peaks at 1.5 V.     

Pd-catalyzed hydrosilylation polymerization of a dihydrosilane with diyne/triyne mixed systems affording crosslinked silylene-divinylene polymers and their properties

Treatment of a dihydrosilane (methylphenylsilane, 1) with mixtures of a diyne (p- or m-diethynylbenzene, 2a or 2b) and a triyne (1,3,5-triethynylbenzene, 3a or B,B′,B″-triethynyl-N,N′,N″-trimethylborazine, 3b; 1:2:3=100:95:5, 100:90:10, 100:80:20) in the presence of Pd-PCy₃ (Cy=cyclohexyl) catalyst gave new crosslinked silylenedivinylene polycarbosilanes. In TGA the resulting crosslinked polymers tended to show higher Td₅ values and higher char yields than the corresponding linear polymers. On the other hand, UV/vis absorption spectra of the crosslinked polymers obtained in the reactions of 2a or 2b with 3a exhibited increased broad peaks around 390 nm for 2a or 360 nm for 2b. Coincidently, their fluorescence spectra showed significant increase of the emission peaks in 400-550 nm. The crosslinked polymer derived from 2a and 3b, however, showed decrease of the absorption peak around 390 nm and profound depression of fluorescence peaks in 400-550 nm.     

Chemical (Sr,Co)-doping effect on critical current density for Dy123 melt-solidified bulks

The dilute impurity doping for CuO-chain site was found to largely improve the critical current properties of both Y123 single crystals and Y123 melt-solidified bulks in our previous study. In addition, dilute Sr-doping to Ba site is also effective for enhancement of J_c without serious decrease in T_c as in the case of dilute Zn doping for CuO₂-plane site. In the present study, we have attempted further enhancement of flux pinning force of the Dy123 melt-solidified bulk, which is essentially more promising materials than Y123, by impurity doping for Cu site in the CuO-chain and for Ba site. Although the (Sr,Co)-co-doped Dy123 melt-solidified bulks showed systematically suppressed T_c with their doping levels, high T_c's well exceeding 90 K were maintained. All the Sr-doped or Co-doped Dy123 bulks exhibited higher J_c than the undoped one. More improved J_c properties were achieved by (Sr,Co)-co-doping, suggesting that pinning potential at local regions around doped impurities become deeper by Co-doping, resulting in stronger point-defect-like pinning sites. In addition, more detailed studies on the dilute Sr-doping and the dilute (Sr,Co)-Co-doping were carried out for Y123 single crystals in order to clarify the difference between their doping effects on the J_c properties. The vortex transition field, H^*, to the disordered state in the M–H loops for the Co-doped Y123 single crystal was located at the lower field than that of the Sr-doped one, meaning that the Co ions strongly affect the vortex system compared with the Sr ions.     

Effect of Gallia Addition on the Sintering Behavior of Samaria-Doped Ceria

Samaria-doped ceria (SDC) was prepared by using the solid-state reaction method. Sintering of SDC was significantly promoted by adding a small amount of gallium. SDC that had 1% of gallium added, sintered at 1450°C, showed almost the same properties as SDC sintered at 1600°C. Measurements showed that the addition of gallia could reduce the sintering temperature by 150°C without deteriorating the properties of SDC as an electrolyte for solid oxide fuel cells.     

Uniaxial elongational viscosity of various molten polymer composites

Uniaxial elongational viscosity of low density polyethylene (LDPE) that was filled with glass bead, glass flake, talc, or glass fiber was measured. The effect of various inorganic fillers on the strain-hardening property in elongational viscosity was investigated. The strain-hardening property of LDPE became weaker by the addition of fillers in the order of glass bead, glass flake, and talc. Glass fiber filled LDPE showed a strain-softening property. The smaller the particle and the larger the aspect ratio, the weaker the strain-hardening property. Their causes were analyzed from the two terms, i.e., the relaxation spectrum and the damping function, by Bernstein-Kearsley-Zapas (BKZ) model. By the incorporation of fillers, the relaxation modules became larger, and the damping function became stronger in the order of glass bead, glass flake, talc, and glass fiber. Recoverable strain was also measured to understand weaker strain-hardening properties. The degree of recovery became smaller by the addition of fillers. It was found that the smaller the particles and the larger the aspect ratio, the smaller the degree of recovery. It was concluded that weaker strain-hardening properties of LDPE composite than that of LDPE are caused by stronger damping function and smaller degree of recovery.     

Monomolecular layer epitaxy of GaAs for ideal static induction transistor

An ideal static induction transistor (ISIT) structure was fabricated using molecular layer epitaxy (MLE). The doping method of MLE enabled us to achieve a sufficiently high level of doping for ISIT fabrication. In the fabrication process a low growth temperature was very important for the device structure, which requires very sharp dopant profiles. For the ISIT, two MLE processes, namely source–drain growth and gate regrowth, were required. The electrical characteristics of the source–drain were changed after heat treatment at a temperature higher than 480°C. The effect of the redistribution of dopants of the source–drain structure (n⁺⁺–i–p⁺⁺–i–n⁺) during gate regrowth was clearly shown by SIMS (secondary ion mass spectroscopy) measurements for various temperatures of heat treatment. As a result the doped Se diffused from the n⁺⁺ source region to the other layers and the doped Zn diffused from the p⁺⁺ layer to the i-layers. The source was a heavily Se-doped layer at the doping level of (2–3)×10¹⁹ cm⁻³ containing a larger amount of interstitial Se atoms in the lattice. The redistribution of Se from the heavily doped region was detectable even after heat treatment at 480°C for 30 min. For the p⁺⁺ layer the profile of the C-doped layer was stable even after heat treatment at 620°C for 30 min, but the profile of Zn changed markedly after heat treatment at 480°C for 30 min. In addition, the carbon-doped p⁺⁺ layer acted as a gettering layer for diffused interstitial Se from the source region. The driving force of the redistribution of dopants results in the electric field in the device structures. © 1997 John Wiley & Sons, Ltd.