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1.
2.
Takaaki Kakitsuka Shinji Matsuo Seok–Hwan Jeong Toru Segawa Hiroshi Okamoto Yoshihiro Kawaguchi Yasuhiro Kondo Yuzo Yoshikuni Hiroyuki Suzuki 《Optical and Quantum Electronics》2006,38(12-14):1053-1060
We theoretically investigated a digitally tunable laser with a chirped ladder filter and a ring resonator to obtain a wide wavelength tuning range covering the whole C- or L- band. The clear relation between the tuning range and laser structure, especially the ladder filter, is described analytically. The introduction of a chirped structure into a ladder filter is effective in achieving both wide tunability and a stable lasing mode. A numerical simulation based on multimode rate equations shows that a tuning range of over 40 nm and a mode suppression ratio over 40 dB can be achieved by introducing a chirped ladder filter. 相似文献
3.
Toru Egawa Yukari Kachi Tsuguhide Takeshima Hiroshi Takeuchi Shigehiro Konaka 《Journal of Molecular Structure》2003,658(3):241-251
The molecular structure and conformation of carvone, a compound with a minty odor, were investigated by means of gas electron diffraction supported by theoretical calculations. Electron diffraction patterns were recorded by heating the nozzle up to 128 °C to obtain enough scattering intensity. The infrared spectrum was also measured by using an absorption cell with a path length of 10 m. The obtained molecular scattering intensities were analyzed with the aid of theoretical calculations and infrared spectroscopy. It was revealed that the experimental data are well reproduced by assuming that carvone consists of a mixture of three conformers that have the isopropenyl group in the equatorial position and mutually differ in the torsional angle around the single bond connecting the ring and the isopropenyl group. It was also found that the puckering amplitude of the ring of carvone is close to those of menthol and isomenthol, a minty compound and its nonminty isomer. The determined structural parameters (rg and ∠α) of the most abundant conformer of carvone are as follows: 〈r(C-C)〉=1.520(3) Å; 〈r(CC)〉=1.360(5) Å; r(CO)=1.225(5) Å; 〈r(C-H)〉=1.104(4)Å; 〈∠CC-C〉=121.1(5)°; 〈∠C-C-C〉=110.4(5)°; ∠C-CO-C=117.1(14)°; 〈∠C-C-H〉=111.1(13)°. Angle brackets denote average values and parenthesized values are the estimated limits of error (3σ) referring to the last significant digit. 相似文献
4.
5.
Shin-ichi Hirano Toshinobu Yogo Wataru Sakamoto Seiji Yamada Tomoyuki Nakamura Tomoe Yamammto Hiroyuki Ukai Kouichi Banno Tomoko Nakafuku Yukari Ando 《Journal of Sol-Gel Science and Technology》2003,26(1-3):35-41
Nano sized crystalline particles/polymer hybrids were synthesized form designed metal-organic precursors. The newly developed method is composed of the synthesis of organic matrix by polymerization and the in situ nucleation and growth of crystalline oxide particles in the organic matrix below 100°C. The design of metal-organic precursor modified with polymerizable ligand and the selection of reaction conditions does influence the size and crystallinity of ceramic particles in organic matrix. The nano-sized magnetic particle/polymer hybrid exhibits the interesting feature of superparamagnetism and quantum size effect. The crystalline particles of BaTiO3/, PbTiO3/, and KNbO3/polymer hybrids behave to be dielectric and show the typical electro-rheological behavior. 相似文献
6.
Highly dispersed molybdena-titania catalyst can be prepared by an equilibrium adsorption method. In this method, molybdate
anions adsorb onto the positively charged titania surfaces via electrostatic attraction by controlling the pH of the impregnating
solution and they increase as an inverse function of the pH. 95Mo-NMR and UV spectroscopic studies of impregnating solution show that the polymeric species like Mo7O24
6-ions are adsorbed on titania in the acidic impregnating solution. XRD, Raman, and XPS data of the calcined samples show that
mono-layer coverage of molybdenum oxide over-layer possesses a highly distorted MoO6 group with a molecular geometry resembling the distorted square pyramid.
The catalytic oxidation of methanol over the surface molybdate species on titania possesses higher turnover numbers and higher
selectivities of partial oxidation products than the catalysts supported on alumina, silica, zirconia, or magnesia. Changes
of the surface properties either after reduction and sulfiding treatment over monolayer catalyst on titania have also been
investigated. The NO chemisorption and XPS studies show that two types of active sites appeared after reduction treatment:
one site is active for hydrogenation of 1,3-butadiene and the other site is active for metathesis of propene. A higher degree
coordinative unsaturations of MO is required for hydrogenation than metathesis. After sulfiding treatments of the catalyst,
hydrogenation of 1,3-butadiene also requires triply coordinative unsaturation, and hydrogenolysis of thiophene requires the
ensemble of doubly or triply coordinative unsaturations. 相似文献
7.
Summary Acetonitrile can be salted-out from aqueous solution by adding tetrabutylammonium perchlorate. This phase separation method has been used for the extraction of the Fe(III)-4,7-diphenylphenanthroline complex into acetonitrile followed by direct injection onto an ODS column. The Fe complex is separated by using 9:1 acetonitrile/water as a mobile phase. The proposed reversed-phase high-performance liquid chromatography has been applied to the determination of Fe in serum. 相似文献
8.
A flow-injection system is described for the determination of d-mannitol. Mannitol dehydrogenase is immobilized on poly(vinyl alcohol) beads and packed in a column (5 cm × 4 mm i.d.). The NADH formed is detected fluorimetrically. The response is linear between 5 × 10?7 and 1 × 10?4 M mannitol and the detection limit is 1 × 10?7 M. The throughput is 30 samples per hour. The reactor is stable for at least 8 weeks. 相似文献
9.
Fluorimetric determination of isatin in human urine and serum by liquid chromatography postcolumn photoirradiation 总被引:2,自引:0,他引:2
For the fluorimetric determination of isatin in human urine and serum, HPLC-postcolumn photoirradiation using a mobile phase has been developed. Isatin in the urine or serum sample was separated on a Capcell Pak C1 column (250 x 4.6 mm id). The mobile phase consisted of 70 mmol l-1 phosphate buffer (pH 7.2)-tetrahydrofuran (85 + 15% v/v) containing 5 mmol l-1 hydrogen peroxide, which was irradiated with germicidal light to induce fluorescence (lambda ex 302 nm, lambda em 418 nm). The addition of tetrahydrofuran to the mobile phase led to the peaks showing good separation as well as increased sensitivity. The calibration graph for isatin was linear over the range of 0.16-10.7 ng. The pretreatment of the acidified urine or serum samples consisted of diluting steps or deproteinizing steps using perchloric acid, respectively. The mean recovery of isatin from urine and serum was greater than 94%. 相似文献
10.
Using a technique of laser flash photolysis coupled with vacuum ultraviolet laser-induced fluorescence spectroscopy, the rate coefficients of O(1D) reactions with N2, O2, N2O, and H2O at 295 ± 2 K have been determined to be , kO2=(4.06±0.24)×10-11, kN2O=(1.35±0.08)×10-10 and . The quoted uncertainties include estimated errors and are the 95% confidence level. The kN2 and kN2O values obtained are larger than the current NASA/JPL recommendations by 26% and 16%, respectively, although they are still within the error limits associated with the recommendations. 相似文献