Grazing-exit and micro X-ray fluorescence analyses for chemical microchips.

Grazing-exit x-ray fluorescence (GE-XRF) and micro x-ray fluorescence (micro-XRF) methods were applied to chemical microchips as a detection method. Since an energy-dispersive x-ray detector was used, the simultaneous detection of multiple elements was possible. An analyzing region was especially designed on the microchip so that a sample solution could be dried and concentrated in a suitable area corresponding to the size of the primary x-ray beam. Finally, it was confirmed that both analytical methods could be combined well for use with a microchip. In GE-XRF, the background intensity in the XRF spectrum was reduced at grazing-exit angles. In addition, a good relationship between the x-ray fluorescence intensities and the concentrations of standard solutions that were introduced into the microchip was obtained. This indicates that the GE-XRF method is feasible for trace elemental analysis in chemical microchip systems. In micro-XRF, an attempt was made to concentrate and dry the analyte within a small analyzing region. The preliminary results indicated that the micro-XRF method could be applied for the analysis of microchips.     

Photon-echo profile in the ultrashort time region for pentacene molecules in crystals

Photon-echo behavior in the ultrashort time region is studied for pentacene molecules in p-terphenyl crystals at 1.7 K by means of the accumulated three-pulse echo. We show highly resolved echo spectra with a parameter of time separation and also time behavior of echo intensity as a function of pulse separation measured at various frequencies near the peak position of the absorption line of the S₀–S₁ transition. We demonstrate various features of echo profile in both time and frequency domains, which are dependent on the time region of observation.     

A new experimental limit for the decay K+ → π+γγ

A search for K⁺ → π⁺γ, π⁺γγ, π⁺γγγ was made detecting pions from stopped kaons in the kinetic energy region between 117 MeV and 127 MeV. New Limits of 1.4 ×10^?6, 8.4 × 10^?6 and 1.0 × 10^?4 for the branching ratio were obtained assuming a phase-space spectrum on the pion energy. The first limit also aplies to another process K⁺ → π⁺ + a, where a is a light meson with mass smaller than 100 MeV/c² and decays into nγ's with lifetime less than 10^?9 s.     

Rapid bonding of Pyrex glass microchips

A newly developed vacuum hot press system has been specially designed for the thermal bonding of glass substrates in the fabrication process of Pyrex glass microchemical chips. This system includes a vacuum chamber equipped with a high-pressure piston cylinder and carbon plate heaters. A temperature of up to 900 degrees C and a force of as much as 9800 N could be applied to the substrates in a vacuum atmosphere. The Pyrex substrates bonded with this system under different temperatures, pressures, and heating times were evaluated by tensile strength tests, by measurements of thickness, and by observations of the cross-sectional shapes of the microchannels. The optimal bonding conditions of the Pyrex glass substrates were 570 degrees C for 10 min under 4.7 N/mm(2) of applied pressure. Whereas more than 16 h is required for thermal bonding with a conventional furnace, the new system could complete the whole bonding processes within just 79 min, including heating and cooling periods. Such improvements should considerably enhance the production rate of Pyrex glass microchemical chips. Whereas flat and dust-free surfaces are required for conventional thermal bonding, especially without long and repeated heating periods, our hot press system could press a fine dust into glass substrates so that even the areas around the dust were bonded. Using this capability, we were able to successfully integrate Pt/Ti thin film electrodes into a Pyrex glass microchip.     

Strictly Transparent Wavelength Conversion Using Multi-Wavelength Signal Generation

We succeeded in strictly transparent wavelength conversion by means of channel selection from multi-wavelength signals generated by sinusoidal modulation of input signal. Modulation-format-independent and bit-rate-independent wavelength conversion is achieved with small power penalty.     

Total synthesis of amauromine

Total synthesis of amauromine ($\text{1}$), a novel alkaloid possessing two reversed prenyl groups in its molecule, was described.     

Fiber Structure,Tensile Behavior and Antibacterial Activity of Polylactide/Poly(butylene terephthalate) Bicomponent Fibers Produced by High-Speed Melt-Spinning

Abstract

Various types of bicomponent fibers composed of polylactide (PLA) and poly(butylene terephthalate) (PBT) with different molecular weights, arranging the polymers separately in the skin or core, were produced by high-speed melt-spinning. The bicomponent spinning, arranging the PLA with high molecular weight (melt flow rate =1.9?g/10?min, L-lactide content = 98.7%) in the skin and the PBT with low molecular weight (IV = 0.835–0.865 dL/g) in the core, resulted in orientation-induced crystallization in the PLA component at the spinning speed of 2?km/min. This crystallization effect was ascribed to a chain-extending treatment applied to the original PLA (MFR = 4.0?g/10?min) to increase its molecular weight. By the treatment the PLA could crystallize when spun even at 1?km/min in its single-component spinning. On the other hand, the bicomponent spinning system interfered with the orientation-induced crystallization of PBT in the core. As a result, the critical spinning speed needed to generate the orientation-induced crystallization in the core PBT was elevated to 4?km/min. The inferior tensile behavior of the bicomponent fibers, as compared to the single-component PLA or PBT fibers, suggested poor compatibility between PLA and PBT. Transesterification reactions rarely occurred at the interface of the two polymers. The bicomponent fibers prepared from high molecular weight PLA and low molecular weight PBT, however, showed sufficient antibacterial activity and physical properties to be suitable for designing medical clothing materials.