A Simple Frequency Lock of Green YAG Laser to Dispersion Line of the Linear Absorption Spectrum of Iodine Molecules Utilizing an Acousto-Optic Frequency Shifter

Frequency of a 532 nm emission line of a diode-laser-pumped Nd:YAG laser is stabilized by lock of the output line to the linear absorption line of iodine molecules. The stabilization method is very simple utilizing the frequency shift caused with an acousto-optic modulator. The laser frequency was stabilized at the zero-crossing point of the second-derivative of the dispersion curve. Instability obtained by the error signal is affected by the phase-characteristics of detectors, which results in 3^*10^-8.     

Development of surface-coil-type resonators consisting of an irradiation and receiver coil system for EPR measurements at 700 MHz

Surface-coil-type resonators (SCRs) consisting of irradiation and receiver coils that are highly isolated from each other were developed for electron paramagnetic resonance (EPR) measurements. Their sample space was open to free space. For these coils, a circular single-turn one-loop receiver coil and a square single-turn twin-loop irradiation coil were fabricated. The transmission lines were set to resonate at about 700 MHz. A phantom (agar, including a nitroxide radical and physiological saline solution) is located on the receiver coil, and the irradiation coil is under the receiver coil. In this condition, the isolation between the receiver and irradiation SCRs was about 40 dB at the resonant frequency. When radiowaves that were divided from the line to the irradiation SCR were applied to the line from the receiver SCR at the appropriate phase and power to cancel the direct coupling between both SCRs, the isolation increased to more than 70 dB. In the conventional SCR, the noise level increased at high incident power. Because such an increase in the noise was not observed in the irradiation-receiver SCR system, high sensitivity at high incident power was obtained.     

Construction of rigid local systems and integral representations of their sections

We give a method for constructing all rigid local systems of semi‐simple type, which is different from the Katz–Dettweiler–Reiter algorithm. Our method follows from the construction of Fuchsian systems of differential equations with monodromy representations corresponding to such local systems, which give an explicit solution of the Riemann–Hilbert problem. Moreover, we show that every section of such local systems has an integral representation. (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Structure of molten selenium by X-ray diffraction

X-ray diffraction patterns have been obtained from molten selenium at 250, 350, 450 and 550°C. The height of the peak maxima in the structure factor was much the same and the first peak maximum was considerably lower than the second one. It was also found that the first peak maximum decreases with the increase of temperature, but the second and third peak maxima are relatively temperature insensitive within the observed temperature range. A comparison between the atomic radial distribution function obtained in this work and that calculated from the quasi-crystalline model was made. From these results, we may suggest that the structure of molten selenium consists mainly of eight-atom ring units randomly distributed.     

Studies of the polymerization of diallyl compounds. XXV. Gel point in the polymerization of diallyl esters of aromatic dicarboxylic acids

Studies on gelation in the radical polymerization of diallyl dicarboxylates have been conducted by Simpson,^9,11 Gordon,¹⁰ and Oiwa.¹³ However, the results obtained have not always been consistent and are still far from full elucidations. In this paper, the gel point in the polymerization of diallyl aromatic dicarboxylates, including diallyl phthalate (DAP), diallyl isophthalate (DAI), and diallyl terephthalate (DAT) is experimentally reexamined in detail and discussed according to Gordon's theory; the discrepancy between actual and theoretical gel point conversion was quite large and was enhanced in the order DAT > DAI > DAP. Moreover, from detailed inquiry into the primary chain length of the prepolymer it is suggested that the intramolecular chain transfer reaction plays an important role in the polymerization of diallyl ester accompanying the intramolecular cyclization reaction. The polydispersity coefficient (P _w,0/P _n,0) of the initial prepolymer of DAP is also estimated to be 2.0 from the extrapolation of P _w/P _n to zero conversion.     

A universal peroxyoxalate-chemiluminescence detection system for mobile phases of differing pH.

A universal peroxyoxalate-chemiluminescence detection system for high performance liquid chromatography, available for a variety of mobile phases, has been developed. The system consisted of a dual-head short-stroke pump and a chemiluminescence detector. The standard conditions using bis(2,4,6-trichlorophenyl) oxalate (TCPO) as aryl oxalate were as follows. The first postcolumn solution was the mixture of 0.5 M imidazole-nitric acid (pH 7.5) and acetonitrile (1:4, v/v). The second was acetonitrile containing TCPO-hydrogen peroxide. These two solutions were delivered by the two pump-heads. After the pH of the column eluate was adjusted to the optimum range (6.5-7.5) by the first postcolumn solution, the solution was mixed with the second postcolumn solution. After flowing through a reaction coil, the chemiluminescence of the mixture was monitored. Using this system, a high sensitivity (fmol level) was obtained for perylene as an analyte with mobile phases having different pH values (2.0-8.0). Polycyclic aromatic hydrocarbons became detectable to a high sensitivity even after the column separation using an acidic mobile phase. The detection sensitivity of nitrated pyrenes after on-line electrochemical reduction using an acidic mobile phase was also increased. This system might be available for other aryl oxalates by some modifications of the postcolumn solutions.     

Einflu? von L?sungsmitteln und Initiatoren auf kationische Copolymerisation von 1,3-Dioxolan mit 5-Methyl-2,3-dihydro-2-furanon

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