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51.
Saka M Iijima K Nishida M Koma Y Hasegawa N Sato K Kato Y 《Shokuhin eiseigaku zasshi. Journal of the Food Hygienic Society of Japan》2008,49(3):160-167
The effects of processing and cooking on the levels of pesticide residues in soybean samples were investigated for 14 pesticides in pre-harvest samples. On soaking, the transfer ratios (%, total pesticide residue amount in product/that in soybean) of soaked soybean were greater than 60% for most of the pesticides investigated. The transfer ratio of soymilk ranged from 37% to 92%, and that of tofu ranged from 7% to 63%. The processing factor (Pf, the concentration (mg/kg) of pesticide in product/that in soybean) of tofu ranged from 0.026 to 0.28. These values varied among pesticides. There was a high correlation between the log P(ow) and the transfer ratio of tofu. The test described here should be useful to obtain the transfer ratios of pesticide residues in processing and/or cooking steps. 相似文献
52.
Masatsune Kato Takaaki Aoki Takashi Noji Yasuhiro Ono Yoji Koike Tomoyuki Hikita Yoshitami Saito 《Journal of Superconductivity and Novel Magnetism》1994,7(1):37-38
We have investigated the relation between the crystal structure and superconductivity in La1.9Bi0.1CuO4+δ , in which the phase separation observed in La2CuO4+δ is suppressed. A phase diagram in theT?δ plane is given for La1.9Bi0.1CuO4+δ with excess oxygen. For very smallδ values, the crystal structure is orthorhombic, and an orthorhombic-tetragonal phase transition occurs markedly atδ ~ 0.03 in the measured temperature range between 13 and 293 K. Superconductivity is observed in the range of 0.04<δ<0.11. This is clear evidence thathigh-T c superconductivity also appears in the tetragonal phase. 相似文献
53.
Yasuhiro Sakuma Masahiko KatoShinya Yagi Kazuo Soda 《Nuclear instruments & methods in physics research. Section B, Beam interactions with materials and atoms》2011,269(3):257-262
We have measured the energy distributions of the secondary ions sputtered from the Si(1 1 1) and Ge(1 1 1) surfaces and investigated the ionization probabilities of sputtered Si+ and Ge+ ions for clarifying their ionization mechanisms. The observed ionization probabilities depend on the velocity of Si+ and Ge+ ions. This velocity dependence can be successfully analyzed by a theoretical expression, which was proposed originally for the metal surfaces. This implies that the ionization mechanism of Si+ and Ge+ ions is the same as ions sputtered from the metal surface, i.e., the resonant electron transfer in the high velocity regime and the thermal excitation process in the low velocity regime. The difference in the ionization probability between Si+ and Ge+ ions is well explained by the difference in the band gap energy. 相似文献
54.
The oxidation of Fe(II) with dissolved molecular oxygen was studied in sulfuric acid solutions containing 0.2 mol . dm-3 FeSO4 at temperatures ranging from 343 to 363 K. In solutions of sulfuric acid above 0.4 mol . dm-3, the oxidation of Fe (II) was found to proceed through two parallel paths. In one path the reaction rate was proportional
to both [Fe2+]2 and po2, exhibiting an activation energy of 51.6 . kJ mol-1. In another path the reaction rate was proportional to [Fe2+]2, [SO4-], and po2 with an activation energy of 144.6 kJ . mol-1. A reaction mechanism in which the SO4- ions play an important role was proposed for the oxidation of Fe(II). In dilute solutions of sulfuric acid below 0.4 mol
. dm-3, the rate of the oxidation reaction was found to be proportional to both [Fe(II)]2 and Po2, and was also affected by [H+] and [SO2-
4]. The decrease in [H+] resulted in the increase of reaction rate. The discussion was further extended to the effect of Fe (III) on the oxidation
reaction of Fe (II). 相似文献
55.
56.
Direct measurement by high-performance size exclusion chromatography with fluorescence detection was applied to the characterization of humic substances in river waters from the Kuji River system, which runs through forest hills and an agricultural plain in Japan. The monitoring wavelength of excitation 320 nm and emission 430 nm corresponds to the fluorescence maxima for aquatic fulvic acid. Chromatograms of the river waters showed four peaks; each peak position was in good agreement among these samples. Peak height ratios for the samples from the upstream Kuji River and its tributaries were different from those of the midstream and downstream sections of the Kuji River, which may reflect differences in the characteristics of humic substances and other organic materials supplied from soil to river. 相似文献
57.
58.
Takehiro Kaneko Yasuhiro Watanuki Takeshi Toyama Yoshiyuki Kojima Nobuyuki Nishimiya 《International Journal of Hydrogen Energy》2017,42(15):10014-10022
In order to enhance hydrogen storage capacity of carbonaceous materials through metal modification, FeNiCr-carbon composites were prepared by calcination of Fe, Ni and Cr-containing polyacrylonitrile (PAN) fibers fabricated by electrospinning method. Fe (III), Ni (II) and Cr (III) acetylacetonates (M (acac)n) were selected as metal sources. Increase of specific surface area and formation of micropores were observed on heat decomposition of M (acac)n particularly through introduction of steam. Maximal hydrogen content, 1.62 mass%, was obtained at 77 K under 0.8 MPa of hydrogen for a FeNiCr-carbon composite, which contained about 15.5 mass% of metals and had specific surface area of 501 m2 g?1. The hydrogen content exceeded the hydrogen physisorption limit, 2.34 mass% per 1000 m2 g?1, which was calculated on the basis of the commensurate–incommensurate transition with an enhancing factor ρ of 1.126. After hydrogenation at 653 K, no hydrogen desorption peaks were observed for FeNiCr powders derived from M (acac)n, and one peak at 828 K for a carbonaceous sample prepared from unmodified PAN fibers. From the most promising FeNiCr-carbon composite, another peak was recorded at 752 K in addition to the peak at 828 K. The former would be originated from hydrogen on novel sorption sites additionally created on the composite formation. 相似文献
59.
This article illustrates two types of organofunctionalized heterogeneous catalysts for variety of organic carbon–carbon bond-forming reactions, summarizing our previous reports and also presenting new data. Organic amines with an alkoxysilane moiety were immobilized on inorganic silica-alumina surfaces (SA-NR2) by simple silane-coupling reactions between the silica-alumina surface (SA) and the alkoxysilane. This SA-NR2 acted as acid–base bifunctional heterogeneous catalysts for carbon–carbon bond-forming reactions, such as cyano-ethoxycarbonylation, Michael reaction of nitriles, and nitro-aldol reaction. These reactions did not occur with either SA or homogeneous amine compounds. In addition, the mixture of SA and homogeneous amine showed low catalytic activity due to undesirable acid–base neutralization reaction. Achiral organic silane-coupling reagents with a variety of functional groups were also immobilized on a SiO2 surface that had been immobilized with chiral bis(oxazoline) (BOX), to which Cu ions were coordinated to make chiral Cu–BOX complexes on the SiO2 surface. The SiO2-supported Cu–BOX complex catalyst functionalized with achiral 3-methacryloxypropyltrimethoxysilane dramatically increased enantioselectivity in the asymmetric Diels–Alder reaction of cyclopentadiene and 3-acryloyl-2-oxazolidinone. The organofunctionalized catalysts showed much better performances for the C–C bond-forming reactions compared to the corresponding homogeneous systems. The heterogeneous catalysts thus obtained were characterized by solid-state 13C and 29Si MAS NMR, FT-IR, UV/vis, XAFS, ESR, XRF, and elemental analysis. 相似文献
60.
Seiichi Takami Yasuhiro Shirai Toyohiro Chikyow Yutaka Wakayama 《Thin solid films》2009,518(2):692-694
We have proposed the synthesis of organic molecular nanowires using porous alumina as a template. We also proposed the use of a magnetic field to control the molecular packing structure in the nanowires. In this paper, we developed the method to evaluate the electronic properties of the nanowire of a phthalocyanine derivative that was synthesized using porous alumina as a template. The developed method facilitates the study in the organic molecular nanowires that were synthesized using templates and helps their use in future electronic devices. 相似文献