Effects of aging and moisture on the dynamic viscoelastic properties of oriental lacquer (urushi) film

The effects of aging and moisture on the dynamic viscoelastic properties of three oriental lacquer films were investigated. With aging over 1000 days at room temperature, the glass‐transition temperature of the lacquer films (T_α) shifted to higher temperatures, the maximum loss tangent (tanδ_α) decreased, and the storage modulus at 20°C (E) increased. These changes were analogous irrespective of lacquers. With increasing moisture content, E decreased and tanδ increased at room temperature. Although the equilibrium moisture content of the virgin lacquer (sap) film was higher than that of the clear lacquer film, its E and tanδ were more stable with an increase of moisture content. It was speculated that the polysaccharides aggregated in the sap film did not effectively contribute to the mechanical properties of the film, while their hygroscopicity resulted in higher moisture content. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2288–2294, 2002     

Residual stress versus microstructural effects on the strength and toughness of phase-separated PbO–B2O3–Al2O3 glasses

A few authors have reasonably proposed that liquid–liquid phase-separated (LLPS) glasses could show improved fracture strength, S_f, and toughness, K_Ic, as the second phase could provide a barrier to crack propagation via deflection, bowing, trapping, or bridging. Due to the associated tensile or compressive residual stresses, the second phase could also act as a toughening or a weakening mechanism. In this work, we investigated five glasses of the PbO–B₂O₃–Al₂O₃ system spanning across the miscibility gap: Four of them undergo LLPS—three are binodal (two B₂O₃-rich and one PbO-rich) and one is spinodal—and one does not show LLPS (composition outside the miscibility gap). Their compositions were designed in such a way that the amorphous particles are under compressive residual stresses in some and under tensile residual stresses in others. The following mechanical properties were determined: the Vickers hardness, ball on three balls (B3B) strength, and toughness, K_Ic-SEVNB (single-edge V-notch beam [SEVNB]). The microstructures and compositions were analyzed using scanning electron microscopy with energy-dispersive X-ray spectrometry. The spinodal glass showed, by far, the best mechanical properties. Its K_Ic-SEVNB = 1.6 ± 0.1 MPa m^1/2, which embodies an increase of almost 50% over the B₂O₃-rich binodal composition, and 90% considering the PbO-rich binodal composition. Moreover, its fracture strength, S_f = 166 ± 7 MPa, is one of the highest ones ever reported for an LLPS glass. Fracture analyses evidenced that the spinodal composition exhibited the lowest net stress at the fracture point. Moreover, calculations indicate that the internal residual stress level is the lowest in the spinodal glass. The overall results indicate that the microstructural effect of the spinodal glass is the most significant factor for its superior mechanical properties. This work corroborates the idea that LLPS provides a feasible and stimulating solution to improve the mechanical properties of glasses.     

Analysis of proton exchange membrane fuel cell catalyst layers for reduction of platinum loading at Nissan

The biggest issue that must be addressed in promoting widespread use of fuel cell vehicles (FCVs) is to reduce the cost of the fuel cell system. Especially, it is of vital importance to reduce platinum (Pt) loading of catalyst layers (CLs) in the membrane electrode assembly (MEA) of a proton exchange membrane fuel cell (PEMFC). In order to lower the Pt loading of the MEA, mass transport of reactants related to the performance in high current density should be enhanced significantly as well as kinetics of the catalyst, which can result in the better Pt utilization and effectiveness. In this study, we summarized our analytical approach and methods for reduction of Pt loading in CLs. Microstructure, mass transport properties of the reactants, and their relation in CLs were elucidated by applying experimental analyses and computational methods. A simple CL model for I–V performance prediction was then established, where experimentally elucidated parameters of the microstructure and the properties in CLs were taken into account. Finally, we revealed the impact of lowering the Pt loading on the transport properties, polarization, and the I–V performance.     

Detection and visualization method of dynamic state transition for biological spatio-temporal imaging data

In the statistical analysis of functional brain imaging data, regression analysis and cross correlation analysis between time series data on each grid point have been widely used. The results can be graphically represented as an activation map on an anatomical image, but only activation signal, whose temporal pattern resembles the predefined reference function, can be detected. In the present study, we propose a fusion method comprising innovation approach in time series analysis and statistical test. Autoregressive (AR) models were fitted to time series data of each pixel for the range sufficiently before or after the state transition. Then, the remaining time series data were filtered using these AR parameters to obtain its innovation (filter output). The proposed method could extract brain neural activation as a phase transition of dynamics in the system without employing external information such as the reference function. The activation could be detected as temporal transitions of statistical test values. We evaluated this method by applying to optical imaging data obtained from the mammalian brain and the cardiac sino-atrial node (SAN), and demonstrated that our method can precisely detect spatio-temporal activation profiles in the brain or SAN.     

Electroelastic Response of Cylindrical Fiber with D∞ Symmetry Exposed to Local Electric Field Through Opposed Electrode Pair

To obtain practical information on the electroelastic behavior of poly-l-lactic acid microtweezers or catheters, a previously constructed analytical technique is used to obtain the electroelastic field solution of a poly-l-lactic acid cylindrical fiber exposed to a local electric field, which is applied through an opposed pair of square-sectioned electrodes. The numerical representation of the solution reveals the detailed field quantity distributions, their importance in the design of microtweezers and catheters, the overall deformation of such devices, and the effects of the electrode dimensions on the deformation.     

Development of 72‐kV high‐pressure air‐insulated GIS with vacuum circuit breaker

SF₆ gas has excellent dielectric strength and interruption performance. For these reasons, it has been widely used for gas‐insulated switchgear (GIS). However, use of SF₆ gas has become regulated under agreements set at the 1997 COP3. Thus, investigation and development for GIS with a lower amount of SF₆ gas are being carried out worldwide. Presently, SF₆‐free GIS has been commercialized for the 24‐kV class. Air or N₂ gas is used as the insulation gas for this GIS. On the other hand, SF₆‐free GIS has not been commercialized for the 72‐kV‐class GIS. The dielectric strengths of air and N₂ gas are approximately one‐third that of SF₆ gas. To enhance the insulation performance of air and N₂ we have investigated a hybrid gas insulation system which has the combined features of providing an insulation coating and suitable insulation gas. We have developed the world's first 72‐kV SF₆‐free GIS. This paper deals with key technologies for SF₆‐free GIS, such as the hybrid insulation structure, a bellows for the high‐pressure vacuum circuit breaker, a newly designed disconnector and spacer, and prevention of particle levitation. Test results of the 72‐kV high‐pressure air‐insulated GIS with the vacuum circuit breaker are described. © 2006 Wiley Periodicals, Inc. Electr Eng Jpn, 157(4): 13–23, 2006; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/eej.20451     

Temperature dependency of bound water of cellulose studied by a high-resolution NMR spectrometer

The widths at half-value of high-resolution NMR spectra of bound water of cellulose were studied in relation to the temperature change. Two points were made clear: First, the amount of bound water of the cellulose sample can be pointed out with higher accuracy the lower the temperature of the measurement. Second, it is possible to determine in a simple manner the boundary temperature T_c at which water molecules become bound by the cellulose. T_c is characteristic of the cellulose sample of a given water content and corresponds to the glass transition temperature of the water-containing sample. The measurements appear to be readily applicable to other hydrophilic polymers.     

Hydrolysis of dextrin in the presence of 12-tungstosilicic acid

Hydrolysis of dextrin in the presence of 12-Tungstosilicic acid was investigated, and the acid was found to show an approximately two times higher catalytic activity than did hydrochloric acid. From the comparison of degree of dissociation of 12-tungstosilicic acid with that of hydrochloric acid, examination of the influence of the ionic strength on the reaction rates, analysis of the reaction products, and evaluation of activation parameters of the reaction, it was assumed in conclusion that the higher catalytic activity of 12-tungstosilicic acid resulted from a “concentration effect” due to the complex formation of the heteropolyanions with dextrin molecules, and from the effect of its higher ionic strength, but not from the effect of direct participation of the heteropolyanion to the elementary reaction process.     

Catalytic action of metallic salts in autoxidation and polymerization: 11. Polymerization of methacrylic acid esters with sodium hexanitrocobaltate in methanol-water

The polymerization of a series of methacrylic acid esters (methyl, ethyl, isopropyl and n-butyl) with sodium hexanitrocobaltate, Na₃[Co(NO₂)₆] was carried out in a methanol-water mixed solvent. The homogeneity of the polymerization system was dependent on the composition of the mixed solvent and greatly affected the rate of the polymerization. A maximum rate was obtained at approximately equimolar fractions of methanol and water in the polymerization of methyl methacrylate. The effect of bulkiness of ester groups on the polymerizability of each monomer was indistinguishable in the mixed solvent system. Kinetic study of the polymerization of methyl methacrylate in a mixed solvent of about an equimolar fraction of methanol and water gave the following polymerization equation: $\text{R}{}_{\mathrm{p}}\text{= k[l]}{}^{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{[}\text{M}\text{]}{}^2$, and an apparent activation energy of 10.6 kcal/mol. The copolymerization of methyl methacrylate and styrene with the initiator suggested that polymerization proceeded via a radical mechanism. The possibility of a certain interaction between initiator, solvent and monomer in the initial stage of the polymerization is discussed on the basis of the kinetic data, properties of oligomers of methyl methacrylate, spectroscopic and other data.