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71.
Masaharu Tsuji Chikashi Yamagiwa Minoru Endoh Yukio Nishimura 《Chemical physics letters》1980,73(3):407-412
The extensive bands observed from the helium afterglow reaction of SO2 in the 250–540 nm region are assigned to the new SO+(A2Π-X2Πr) system produced from the He+/SO2 dissociative charge-transfer reaction at thermal energy. They had been erroneously interpreted as the SO+2 (C?-X?) system produced from He(23S)/SO2 Penning ionization. The spectroscopic constants for the SO+A2Π) and SO+(X2Πr) states were determined. 相似文献
72.
Naofumi Terada Minoru Morimoto Hiroyuki Saimoto Yoshiharu Okamoto Saburo Minami Yoshihiro Shigemasa 《先进技术聚合物》2003,14(1):40-51
Oxidized chitosan derivatives with various degrees of oxidation (DS, 0.1–1.0) were prepared by the treatment of chitosan with CrO3/aq HClO4 or by the oxidation of 3‐O‐ and N‐protected chitosan with 30% aq H2O2/Na2WO4 followed by 3‐O‐ and N‐deprotection. The oxidized products were then N‐acetylated with Ac2O in order to improve their water‐solubility. Although the oxidized chitosan derivative of DS 0.28 and the degree of N‐acetylation of chitosan (DA) 38% was insoluble in the pH 3–8 region, that of DS 0.26 and DA 76% was soluble in the neutral pH range. The newly‐prepared acetylated and oxidized chitosan derivatives were found to suppress the chemiluminescence response of inflammatory cells such as canine polymorphonuclear cells (PMNs). Analysis by the surface plasmon resonance method revealed that the bind and release behavior of PMNs to acetylated oxidized chitosan derivatives was similar to that against carboxymethylated chitosan derivatives. The amount of water‐soluble chitosan derivative bound to cytokine IL‐8 was found to be affected by the structural and electronic features of the chitosan substituents in the chitosan chain. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
73.
Minoru Tanaka Masanobu Yoshinaga Satoshi Asano Yuko Yamashoji Yoshihiro Kawaguchi 《Fresenius' Journal of Analytical Chemistry》1992,343(12):896-900
Summary The enantiomeric separation ability of unmodified and methylated cyclodextrins (CDs) during capillary zone electrophoresis (CZE) was investigated using twelve dansylamino acids. Unmodified - and -CDs exhibited high enantioselectivities. -CD could scarcely separate the enantiomers before and after dimethylation, but obtained enantioselectivity after trimethylation. On the other hand, dimethylation of -CD removed much of its high enantioselectivity. Moreover, the chemical modifications produced a reverse in the migration order of the enantiomers. The inclusion of dansyl-DL-phenylalanine with CDs was evaluated using 600 MHz 1H NMR spectroscopy. 相似文献
74.
Determination of 4-alkylphenols by novel derivatization and gas chromatography-mass spectrometry 总被引:2,自引:0,他引:2
A simple and sensitive method for the determination of alkylphenols in water samples has been developed using gas chromatography-mass spectrometry. Alkylphenols were determined after the extractive derivatization with pentafluoropyridine. The derivatization of alkylphenols efficiently proceeded to give the corresponding 4-tetrafluoropyridyl derivatives under the biphasic reaction system. The derivatization conditions including the phase-transfer catalyst, the amount of pentafluoropyridine, the reaction time, the concentration of NaOH and organic solvent were optimized. On the mass spectra of these derivatives, intense specific ion peaks were observed: m/z 256 for 4-n-alkylphenols and m/z 284 for 4-tert.-alkylphenols. Calibration curves were linear in the range of 20-1000 ng/l (200-10,000 ng/l for nonylphenol), and the detection limits varied between 6.93 and 15.7 ng/l (85.2 ng/l for nonylphenol). The average recoveries of the alkylphenols in a fortified river water sample (100 ng/l except for nonylphenol: 1000 ng/l) ranged from 91.1 to 112%. The relative standard deviations were found to be between 5.6 and 16%. This method was successfully applied to the determination of alkylphenols in river water. 相似文献
75.
Atsuhisa Mimoto Sojiro Kon Takuya Motomura Minoru Inaba 《Journal of fluorine chemistry》2005,126(7):1101-1110
The Ni-based alloys, such as Ni-Co, Ni-Mn, Ni-Ag, Ni-Cu, Ni-Al and Ni-Si, prepared by hot isostatic pressing (HIP) at 1000 °C under 2 × 108 Pa for 2 h were employed as the anodes for electrolytic production of NF3. The current efficiencies for NF3 formation were 42-38, 52-40, 52-47, 63-62, 50 and 41% for Ni-Co, Ni-Mn, Ni-Ag, Ni-Cu, Ni-Al and Ni-Si alloys, respectively. The current efficiencies only on Ni-Cu alloys with Cu concentrations lower than 10 mol% were almost the same as those on Ni sheet and HIPed Ni anodes, whereas those on the other alloys used in this study were smaller compared with those on both Ni anodes. On the other hand, the current losses caused by anodic dissolution of Ni-Co, Ni-Mn, Ni-Ag, Ni-Cu, Ni-Al and Ni-Si alloy electrodes were 7.95-4.42, 6.40-7.02, 5.60-6.30, 3.34-6.33, 5.10 and 0.18%, respectively. The anode consumptions of Ni-5 mol% Cu and Ni-5 mol% Si alloys were almost the same or smaller compared with those of Ni sheet and HIPed Ni electrodes, though those of other alloys used were large compared with those of both Ni anodes. Consequently, addition of Cu to the nickel matrix is available for a cheaper cost of anode with keeping a same current efficiency as that on the Ni anode and addition of Si to the nickel matrix is effective for decreasing anode consumption largely. A Ni sheet electrode containing a trace of impurities, such as Co, Mn, Ag and Al, is also favorable as the anode for electrolytic production of NF3. 相似文献
76.
We have shown the Lennard-Jones (LJ) phase diagram for a slit-shaped nanopore by molecular simulations and thermodynamically
predicted the results with no adjustable parameter. With this success, LJ phase diagrams are predictable. In this study, the
freezing of an LJ CH4 capillary condensate under a tensile condition in a nonstructural carbon nanopore with a cylindrical geometry was examined
using molecular dynamics (MD) simulation. We employ a unit cell in contact with a bulk vapor phase, which is useful for the
determination of the bulk vapor pressure in equilibrium with the molecules in a pore. The MD simulation results show liquid-solid
(amorphous) phase transitions with a variation in the bulk vapor pressure. The frozen particles are arranged in concentric
circular regions along the wall similar to those reported by Maddox and Gubbins. The freezing points are determined from the
variations in density, enthalpy, arrangement, and structural functions. The obtained liquid-solid coexistence points are found
to exhibit a significant dependence of the freezing point on the equilibrium bulk vapor pressure, forming an extraordinarily
skewed curve on the p-T diagram, in contrast to the bulk phase coexistence that is represented by an almost vertical line.
The origin of the significant dependence is considered to be the Laplace effect on the capillary condensate similar to the
case with a slit-shaped pore. A simple model, which the authors earlier presented for slit-shaped nanopores, successfully
predicted the p-T relation of the freezing point for cylindrical nanopores as well. 相似文献
77.
Kazuo Sugiyama Tadao Nakaya Minoru Imoto 《Journal of polymer science. Part A, Polymer chemistry》1972,10(1):205-215
A study of the photopolymerization of vinyl monomers in the presence of tetramethyltetrazene (TMT) was made. TMT was found to act as an effective sensitizer. In the photopolymerization of vinyl monomers such as methyl methacrylate or styrene the rate of polymerization was expressed by the equation: Rp = k[TMT]1/2[monomer]. The chain-transfer constant of TMT under ultraviolet irradiation was estimated to be 3.8 × 10?2 for the above monomers. A linear correlation was found to exist between the reactivity of dimethylamino radical toward the vinyl monomers and e values for the corresponding monomers. 相似文献
78.
A new synthetic method for the preparation of allyl amines has been developed. The key steps of this method are enantioselective addition of diethylzinc and [1,3]-chirality transfer through the [3.3] sigmatropic rearrangement of allyl cyanates. Stereocontrolled syntheses of lentiginosine (1) and polyoxamic acid derivative 2 from a common intermediate 7 derived from D-tartaric acid (8), have been accomplished. 相似文献
79.
A novel pressure-driven sample injection method was developed as an alternative to electrokinetic injection, and electrophoretic separation was carried out on a microfabricated device employing this method. This method enables a defined volume of liquid dispensing, followed by instantaneous injection driven by pneumatic pressure, greatly simplifying the injection procedure. A particular microstructure, called a "metering chamber", has been designed for the quantitative dispensing of an ultra-low volume of sample liquid; a "hydrophobic passive valve" equipped with an air vent channel is employed for injecting a dispensed sample into the separation channel. The reproducibility of dispensing was 3.3% (n = 15), expressed by the variation of dispensed volumes. The electrophoretic separation of DNA fragments was performed using this injection method, varying the injection volumes from 0.45 to 4.0 nL, and the separation efficiencies were compared. This precise injection method, easily variable in injection volumes, is highly suitable for quantitative as well as qualitative electrophoretic analyses. 相似文献
80.
Abstract The reaction of aluminum alkoxide in straight-chain primary alcohols at elevated temperatures yielded the alkyl derivatives of boehmite [AlO(OH)1-x (OR) x ], a class of intercalation compound where the guest moieties are covalently bonded to the host boehmite layers. The addition of small amounts of water to the reaction system yielded another phase having a larger basal spacing. XRD, IR, and elemental analysis showed that the products had the boehmite layer structure with the alkyl moieties incorporated between the boehmite layers. IR spectra of the products also exhibited bands due to hydrogen bonding between the boehmite layers. These results suggest that the products are the alkyl derivatives of boehmite having the second stage structure. Because water in the reaction medium facilitated the hydrolysis of intermediate aluminum alkoxides, the product with the second stage structure had smaller alkyl/Al ratio and therefore had smaller basal spacing than that expected from the corresponding first stage product. 相似文献