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61.
R. Nishi I. Houda K. Kitano Y. Sugawara S. Morita 《Applied Physics A: Materials Science & Processing》2001,72(7):S93-S95
Noncontact imaging was successfully performed with the quartz resonator in air by using the FM detection method. A constant frequency shift mode was used. The frequency shift was about -30 mHz, which was induced by the attractive force gradient. A noncontact image of the Si(111) atomic step was obtained with vertical and lateral resolutions of 0.8 Å and 60 Å. 相似文献
62.
M Yoshikawa H Endo K Hoshino Y Sugawara O Takaiti S Kanda K Imai 《Biomedical chromatography : BMC》1990,4(5):181-187
A new method for the high performance liquid chromatographic (HPLC) determination of N-(N-acetyl-L-methionyl)-O,O-bis(ethoxycarbonyl)dopamine (TA-870), a dopamine prodrug, in biological fluid has been developed. In order to measure with an electrochemical detector (ECD), TA-870 was passed first through an immobilized carboxylesterase column to be converted to the electrochemically active deethoxycarbonylated TA-870 (DEC-TA-870). The properties of this carboxylesterase immobilized on Sepharose 4B were examined by this flow injection system. Hydrolysis of TA-870 with this immobilized carboxylesterase was a maximum at pH 7-8 and 50 degrees C, and the activity decreased in the presence of organic solvent such as acetonitrile. For the determination of TA-870 in biological fluids, an HPLC-immobilized enzyme-ECD system using a column-switching technique was developed. The blood was deproteinized with ethanol, and TA-870 in the ethanol extracts was adsorbed in Bond Elut C18. The dichloromethane eluate from Bond Elut C18 was injected into the HPLC system. The HPLC apparatus was composed of three pumps, two separation columns (LiChrosorb Si 60 and mu Bondasphere), a trap column (Bond Elut), an enzyme column, ECD and the column-switching system. The calibration curve for TA-870 in blood was linear in the range from 2 to 200 ng/mL. This new assay method might be useful also for the determination of other catechol ester compounds. 相似文献
63.
64.
Kapuruge Don Kunkuma Amila Somarathne Ekenechukwu C. Okafor Daiki Sugawara Akihiro Hayakawa Hideaki Kobayashi 《Proceedings of the Combustion Institute》2021,38(4):5163-5170
This study examined the effects of OH concentration and temperature on the NO emission characteristics of turbulent, non-premixed methane (CH4)/ammonia (NH3)/air swirl flames in two-stage combustors at high pressure. Emission data were obtained using large-eddy simulations with a finite-rate chemistry method from model flames based on the energy fraction of NH3 (ENH3) in CH4/NH3 mixtures. Although NO emissions at the combustor exit were found to be significantly higher than those generated by CH4/air and NH3/air flames under both lean and stoichiometric primary zone conditions, these emissions could be lowered to approximately 300 ppm by employing far-rich equivalence ratios (?) of 1.3 to 1.4 in the primary zone. This effect was possibly due to the lower OH concentrations under far-rich conditions. An analysis of local flame characteristics using a newly developed mixture fraction equation for CH4/NH3/air flames indicated that the local temperature and NO and OH concentration distributions with local ? were qualitatively similar to those in NH3/air flames. That is, the maximum local NO and OH concentrations appeared at local ? of 0.9, although the maximum temperature was observed at local ? of 1.0. Both the temperature and OH concentration were found to gradually decrease with the partial replacement of CH4 with NH3. Consequently, NO emissions from CH4/NH3 flames were maximized at ENH3 in the range of 20% to 30%, after which the emissions decreased. Above 2100 K, the NO emissions from CH4/NH3 flames increased exponentially with temperature, which was not observed in NH3/air flames because of the lower flame temperatures in the latter. But, the maximum NO concentration in CH4/NH3 flames was occurred at a temperature slightly below the maximum temperature, just as in NH3/air flames. The apparent exponential increase in NO emissions from CH4/NH3 flames is attributed to a similar trend in the OH concentration at high temperatures. 相似文献
65.
Kotaro Nagatani Yunosuke Hoshino Haruka Tezuka Masahisa Nakada 《Tetrahedron letters》2017,58(10):959-962
A synthetic pathway to the C-ring fragment of cotylenin A which emerged from our retrosynthetic analysis of cotylenin A is described. The catalytic asymmetric intramolecular cyclopropanation (CAIMCP) of the α-diazo-β-keto ester bearing 2,4,6-trimethylphenyl group as the ester part has been found to afford the crystalline product with high ee, which allowed to establish the approach to the C-ring fragment which required ten-pot operations. The developed approach would be beneficial to a large scale synthesis of the C-ring fragment for the total synthesis of cotylenin A. 相似文献
66.
Wang J Sugawara A Shimojima A Okubo T 《Langmuir : the ACS journal of surfaces and colloids》2010,26(23):18491-18498
A facile solution process for the preparation of anisotropic silica nanoparticles (ASNPs) is presented. ASNPs are prepared via controlled self-assembly of spherical silica seeds (22 nm) in alcohol-water mixed media, followed by their in situ fixation and overgrowth with tetraethoxysilane (TEOS). Ethanol and L-arginine (Arg) are used to modify the dielectric constant and ionic strength of the reaction media, by which seed assembly is controlled through the adjustment of electrostatic interaction. Ethanol and Arg also serve as a cosolvent and a catalyst for hydrolysis and condensation of TEOS, respectively, which enables us to produce ASNPs in a simple one-pot process. In addition to ASNPs with wormlike structures, different kinds of NPs (bimodal spherical NPs, monodisperse spherical NPs, and spherical aggregates) have also been obtained by changing the concentrations of ethanol and Arg. The length, thickness, or both of ASNPs are controlled systematically by varying the concentrations of Arg, seed NPs, and TEOS. Other alcoholic cosolvents, such as methanol, 1-propanol, 2-propanol, and t-butanol, are also effective to give ASNPs when the dielectric constant of the alcohol-water mixed media is properly adjusted, showing the versatility of the present method. 相似文献
67.
To evaluate the superiority of using a task-specific onium salt (TSOS), a novel TSOS reagent 1-methyl-3-[2-(8-quinolinylaminosulfonyl)ethyl]imidazolium chloride (HmimesqCl) was synthesized, and its performance in extraction of different divalent metal cations was investigated. This TSOS reagent has both a cationic imidazolium unit and an anionic (proton-dissociable) complexation unit for the extraction of metal cations into an ionic liquid. In the use of HmimesqCl, relatively high extraction of metals resulted in comparison with the use of its non-imidazolium analogs, without changing the extraction selectivity. 相似文献
68.
We report the construction of a molecular recognition layer composed of polyelectrolyte brushes and metal complexes on the surface of a quartz crystal microbalance (QCM) and the sensing abilities for various volatile organic compounds (VOCs). Atom‐transfer radical polymerization of 2‐(dimethylamino)ethyl acrylate from an initiator‐terminated self‐assembled monolayer yielded polyelectrolyte brushes on the surface of a weight‐detectable quartz crystal microbalance. One end of a poly[(2‐dimethylamino)ethyl methacrylate] brush was covalently attached onto the surface of a sensor. We found that metallophthalocyanines with four bulky pentaphenylbenzene substituents could adsorb volatile organic compounds selectively into their cavities. Macromolecular metal complexes were prepared by immersing polymer‐brush‐modified QCMs into an aqueous solution of sterically protected cobalt phthalocyanine. Anionic cobalt phthalocyanine was trapped in the polymer brushes and acted as a molecular receptor for the sensing of VOC molecules. 相似文献
69.
The visible second harmonic of the idler output from a noncollinear optical parametric amplifier was compressed using adaptive dispersion control with a deformable mirror. The amplifier was pumped by and seeded in the signal path by a common 400 nm second-harmonic pulse from a Ti:sapphire regenerative amplifier. Thus, both the idler output and the second harmonic of the idler were passively carrier-envelope phase stabilized. The shortest pulse duration achieved was below 3 fs. 相似文献
70.
We have developed efficient electrocatalysts for methanol oxidation using new synthetic method facilitating deposition of Pt–Ru very thin nanoplatelets on carbon nanoparticles The method involves oxidation of carbon support, adsorption of Pb2+, its reduction and galvanic displacement of Pb0 by Pt and/or Ru. The Pt mass activity of this catalyst is about 10 times higher than that of the commercial Pt–Ru/C. The catalyst with the 1:1 Pt/Ru ratio displayed the highest methanol oxidation activity per surface Pt atom. Our results demonstrate the new synthetic method that yields the catalyst with potential for solving the problem of high Pt loading in direct methanol fuel cell anodes. 相似文献