Multiwavelength distributed-feedback dye laser array and its application to spectroscopy

A multiwavelength, multistripe tunable laser array is proposed, and its application to absorption spectroscopy is demonstrated. Laser waveguides doped with Rhodamine 6 G dye were integrated on a plastic chip, and simultaneous output at different wavelengths was obtained by use of a distributed-feedback technique. A very low threshold of 3 muJ was attained, and spectrally narrowed output (<0.1 nm) was obtained. A scheme for digital spectroscopy is also proposed based on this laser array, and absorption spectroscopy of sodium atoms without wavelength scanning is demonstrated by use of a sodium-vapor cell.     

Mechanical and dielectric absorption of poly(vinyl chloride) and some related polymers

The mechanical and dielectric low temperature absorptions of poly(vinyl chloride) (PVC) and several modified PVC's have been studied over the temperature range from ?60 to +60°C. with some tests extending to ?150°C. and others to +170°C. The results indicate that the low-temperature absorption near ?50°C (β₂ absorption) decreases in intensity with chlorination, while the absorption at a higher temperature near 0°C (β₁ absorption) decreases in intensity with hydrogenation. The apparent activation energies of the β₁ and β₂ absorptions were calculated to be 16 kcal/mole and 10.7 kcal/mole, respectively. Besides, the β₂ absorption markedly decreases in intensity with addition of plasticizer, while the intensity of β₁ absorption is not much affected by increasing plasticizer content. From these results, the β₁ and β₂ processes are concluded to be the results of molecular motion in crystalline and amorphous region in PVC, respectively. For samples of reduced Cl content, another low-temperature absorption was located near ?120°C (γ absorption) and attributed to the presence of short sequences of ethylene units. It has also been observed that the temperature location of the high temperature absorption near 100°C (α absorption) shifts linearly to higher temperature with increasing chlorine content and to lower temperature with increasing hydrogen content.     

Spatial study on a multibubble system for sonochemistry by laser-light scattering

Volumetric oscillation of multiple cavitation bubbles in an ultrasonic standing-wave field is investigated spatially through the intensity measurements of scattered light from bubbles changing the measuring position in the direction of sound propagation. When a thin light sheet finer than half of wavelength of sound is introduced into the cavitation bubbles, at an antinode of sound pressure the scattered light intensity oscillates. The peak-to-peak light intensity corresponds to the number of the bubbles which contribute to the sonochemical reaction because the radius for oscillating bubbles at pressure antinodes is restrictive in a certain range due to the shape instability and the action of Bjerknes force that expels from the antinode bubbles that are larger than the resonant size. The experimental results show that the intensity waveform of oscillating scattered light measured at the side near the sound source is similar to the waveform as seen in a single-bubble experiment. The peak-to-peak light intensity for the scattered light waveform is low at the side near the sound source where the progressive wave is dominant, while at the side near the water surface far from the sound source the intensity is relatively high and has periodic structure corresponding to the periodicity of half wavelength from the standing wave. These tendencies of high intensity near the water surface and the periodicity correspond to the periodic luminescent stripes seen in images of luminescence in an ultrasonic standing wave as reported by Hatanaka et al. [Jpn. J. Appl. Phys. 39 (2000) 2962]. The present method of light scattering is promising for evaluating spatial distribution of violently oscillating cavitation bubbles which effect sonochemical reactions.     

Common-path achromatic interferometer-coronagraph: nulling of polychromatic light

A three-dimensional common-path interferometer is proposed, which can achromatically null out an on-axis source while it maintains the detectability of an off-axis source. A geometric phase in the three-dimensional interferometer introduces an achromatic pi-phase shift to the light from the on-axis source, such that destructive interference nulls out the axial light at one of the ports of the interferometer. Light from the off-axis source, which is exempt from the pi-phase shift, comes out from both ports with equal intensity. The common-path scheme makes the system highly immune to environmental disturbances.     

O-selectivity and utility of phosphorylation mediated by phosphite triester intermediates in the N-unprotected phosphoramidite method

Previously, O-selective phosphorylation on polymer supports in the N-unprotected phosphoramidite method could not be carried out because the amino groups of dA and dC have high reactivity toward tervalent phosphorus(III)-type phosphitylating reagents. In this paper, we developed a new coupling strategy named the "activated phosphite method" in which the phosphitylation is mediated by phosphite triester intermediates 1. Application of 1-hydroxybenzotriazole as the promoter to the solid-phase synthesis resulted in excellent O-selectivity of more than 99.7%. This O-selectivity was explained by the frontier molecular orbital interactions between the reactive intermediates and the nucleophiles such as the amino or hydroxyl groups of nucleosides. Furthermore, longer oligonucleotides were synthesized not only by a manual operation but also by a DNA synthesizer. The utility of our new method was demonstrated by the successful synthesis of a base-labile modified oligodeoxyribonucleotide having 4-N-acetyldeoxycytidine residues. Finally, DNA 20-mers containing dA or dC could be synthesized in good yields by use of a combined reagent of 6-trifluoromethyl-1-hydroxybenzotriazole and benzimidazolium triflate.     

Memory effect in the chain-collapse process in a dilute polymer solution

The effect of temperature perturbation on a single-chain-collapse process was studied for poly(methyl methacrylate) with the molecular weight M(w)=1.05 x 10(7) in the mixed solvent of tert-butyl alcohol+water (2.5 vol %). In the chain-collapse process after a quench from the theta; temperature to a temperature T(1), the temperature was changed from T(1) to T(2) at the time t(1) after the quench and returned to T(1) at the time t(1)+t(2). In the three stages at T(1), T(2), and T(1), measurements of the mean-square radius of gyration of polymer chains were carried out by static light scattering and the chain-collapse process was represented by the expansion factor as a function of time. An effect of chain aggregation on the measurements was negligibly small because of the very slow phase separation. For the negative temperature perturbation (T(1)>T(2)), the chain-collapse processes observed in the first and third stages were connected smoothly and agreed with the collapse process due to a single-stage quench to T(1). A memory of the chain collapse in the first stage at T(1) was found to persist into the third stage at the same temperature T(1) without being affected by the temperature perturbation of T(2) during t(2). The memory effect was observed irrespective of the time period of t(2). The positive temperature perturbation (T(1)相似文献