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71.
72.
S. M. Abdur Razzak Yoshinori Namihira Kazuya Miyagi Feroza Begum Shubi Kaijage Nguyen Hoang Hai Tatsuya Kinjo Nianyu Zou 《Optical Review》2007,14(1):14-16
This paper presents a novel technique for the control of chromatic dispersion and confinement loss in hexagonal photonic crystal
fibers (H-PCFs). It is demonstrated that it is possible to obtain very low chromatic dispersion of 0 ± 0:38 ps/(nm·km) in
the wavelength range of 1.41 to 1.66 μm and confinement loss of less than 0.0001 dB/km from a six ring modified H-PCF (MH-PCF).
The higher order dispersion at 1.55 μm is about −0.001 ps/(nm2-km). 相似文献
73.
Taketoshi Matsumoto Patricia Nickut Kazuya Watanabe Tatsuya Tsukuda Katharina Al-Shamery 《Surface science》2007,601(22):5226-5231
Reduction of oxidized gold nanoclusters by exposures to foreign gases and irradiation of UV photons has been investigated using X-ray photoelectron spectroscopy. Gold nanoclusters with narrow size distributions protected by alkanethiolate ligands were deposited on a TiO2(1 1 0) surface with dip coating. Oxygen plasma etching was used for removal of alkanethiolate ligands and oxidization of gold clusters. The oxidized gold clusters were exposed to CO, C2H2, C2H4, H2, and hydrogen atoms. Although, C2H4 and H2 did not show any indications of reduction of oxidized gold clusters, CO, C2H2, and hydrogen atoms reduced the oxides on gold cluster surfaces. Among them, hydrogen atoms were most effective for reduction. Irradiation of UV photons around 400 nm could also reduce the oxidized gold clusters. The photochemical reduction mechanism was proposed as follows. The photo-reduction was initiated by electronic excitation of gold clusters and oxygen atoms activated reacted with carbon atoms at the surfaces of gold clusters. Carbon species were likely absorbed in gold clusters or remained at the boundaries between gold clusters when gold clusters agglomerated during oxygen plasma exposures. As the photochemical reduction progressed, carbon atoms segregated to the surfaces of gold clusters. 相似文献
74.
Chen Rong Kazuya Mitsuji Xue Songtao Yoshihiro Sugimura Masanori Izumi 《Acta Mechanica Solida Sinica》1999,12(2):144-154
The purpose of this paper is to study the dynamic behavior of soft ground including a porous layer by considering the porosity
change. In order to take the porosity change into account, the concept of the volume fraction, which has been proposed in
continuum mechanics, is introduced. The constitutive equations presented by Bowen are applied to the analysis of the porous
media. According to Bowen's theory, the porosity is considered as a variable called the volume fraction and has its own constitutive
equation. The constitutive equation of the volume fraction has thermoelastic equation coefficients and is determined by the
strains of the solid and the fluid. This means that the compressibilities of the solid and the fluid are considered. When
the special condition is assumed, Bowen's theory can contain Biots's theory, which has been applied in earthquake engineering.
The wave propagation in the ground including a porous layer, modeled by Bowen's theory, is studied and compared with that
of Biot's theory. One-dimensional attenuation and surface amplitude are calculated. The effect of the volume fraction is discussed
with respect to the compressibilities of the solid and the fluid. 相似文献
75.
Kiyotomi Kaneda Kazuya Yamaguchi Kohsuke Mori Tomoo Mizugaki Kohki Ebitani 《Catalysis Surveys from Japan》2000,4(1):31-38
Various Mg-Al type hydrotalcites were examined as catalysts for the epoxidation of olefins and N-oxidation of pyridines using hydrogen peroxide. The catalytic activity of hydrotalcites increased with increasing the basicity of their surface. Adding cationic surfactants, e.g., n-dodecyltrimethylammonium bromide, to the above system remarkably accelerated the reaction rate. The hydrotalcites, into which were introduced both Ru and Co cations in the Brucite layers, were found to be good catalysts for the oxidation of various alcohols in the presence of molecular oxygen. Moreover, these hydrotalcites could smoothly catalyze also the oxygenation of diphenylmethane, fluorene, and xanthene at benzylic position with excellent yields. The hydrotalcite catalysts could be easily separated from the reaction mixture and reused with retention of their high catalytic performance for the above oxidations. 相似文献
76.
77.
78.
Masashi Haruki Fumiya Kobayashi Kazuya Kishimoto Shin-ichi Kihara Shigeki Takishima 《Fluid Phase Equilibria》2009,280(1-2):49-55
A new apparatus based on the circulation method was developed to measure the solubility of metal complexes in supercritical carbon dioxide (scCO2) at a wide range of temperatures and pressures. A UV–vis spectrometer, which was connected to a small saturation cell through optical fibers, was used to determine solubility. The solubilities of cobalt(III) acetylacetonate (Co(acac)3) and chromium(III) acetylacetonate (Cr(acac)3) in scCO2 were measured to check the validity of both the apparatus and the method and to accumulate new solubility data. The solubility data for Cr(acac)3 obtained in this study were in good agreement with the data reported in the literature.The measured solubilities of Co(acac)3 and Cr(acac)3 were also correlated with the empirical equation including the three adjustable parameters, based on the equation proposed by Chrastil. The parameters were determined by fitting the equation to the experimental data for each metal complex and the calculated results closely replicated the experimental data. 相似文献
79.
It was observed that the reaction of CFCl3 with thiophenoxide gave only 10% of the corresponding thioether. On the other hand, these thioethers could be prepared in excellent yield from diaryl disulfides and CFCl3 in the presence of sodium hydroxymethanesulfinate in aqueous DMF at 4 atm pressure of nitrogen. Dechlorination of the thioether (PhSCFCl2) with different reducing agents were studied. Most of the reducing agents eliminated both fluorine and chlorine functionalities or gave the hydrolyzed products. But its sulfone on treatment with Zinc in methanol gave monochlorofluoromethyl and fluoromethyl phenyl sulfone in good yields. Darzens reaction of these compounds was also studied. 相似文献
80.
Abstract Using supercritical water oxidation, the cation exchange resin was decomposed fast and completely to water, carbon dioxide and sulfuric acid. While the resin decomposition yield increased with the reaction time and the amount of hydrogen peroxide added as oxidizing agent, it was constant in the resin concentration from 0.14 to 1.9 dry resin weight percent to water. More than 99% of the cation exchange resin was decomposed with hydrogen peroxide added in the amount of 7 times the stoichiometric value at 673 K and 30MPa for 30 minutes of the reaction time. The cation exchange resin is decomposed through two main reaction pathways. One has a rate controlling intermediate such as acetic acid whose decomposition rate was very slow, and the other does not have stable intermediates. The decomposition of the acetic acid is a significant factor for the complete decomposition of the resin, although it does not dominate the whole resin decomposition. A simple kinetic model that estimates the resin decomposition yield was developed. 相似文献