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21.
Atsushi Takahashi Isao Nakamura Masaaki Haneda Tadahiro Fujitani Hideaki Hamada 《Catalysis Letters》2006,106(3-4):133-138
Catalytic hydrogenation of naphthalene to decalin was studied over a carbon-supported rhodium catalyst in supercritical carbon
dioxide solvent at 333 K, and the results were compared with those in an organic solvent. cis-, trans-Decalin and tetralin were formed from the beginning of the reaction in supercritical carbon dioxide. Higher concentration
of hydrogen in carbon dioxide solvent and on the active site, and also the suppression of desorption of partially hydrogenated
tetralin molecules from the active site would be responsible for higher selectivity to cis-decalin in supercritical carbon dioxide than that in an organic solvent. 相似文献
22.
Photon rupture with a focused single pulse of pulsed YAG-laser irradiation was used to fabricate an aluminum electrochemical micro-reactor. Porous type anodic oxide film formed on aluminum specimens was irradiated in solutions with a pulsed Nd-YAG laser beam through a convex lens to fabricate micro-channels, micro-electrode, and through holes (for reference electrode, solution inlet, and outlet). During irradiation, specimens were moved by a computer controlled XYZ stage. After irradiation, the surface of the micro-channel and through hole were again treated to form anodic oxide film and the surface of the micro-electrode was treated electrochemically to provide an Au layer. The calculated volume of the micro-reactor including micro-channel and through holes is about 1.5 μl. The cyclic voltammogram of the micro-electrochemical cell was measured in K3Fe(CN)6/K4Fe(CN)6 with both static and flowing solution at different scanning rates. The anodic and cathodic peak currents were measured and the values depended on scanning rate and ion concentration when the solution was static. With the flowing solution, limiting currents were observed and the anodic limiting current was increased with the cubic root of the solution flow rate. 相似文献
23.
Alain A Vertès Masayuki Inui Hideaki Yukawa 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2007,82(8):693-697
The challenges of implementing biorefineries on a global scale include socioeconomic, financial, and technological constraints. In particular, the development of biorefineries is tightly linked to the continued availability of fermentation raw materials. These constraints can be relaxed by the use of diverse raw materials, while advances that confer higher flexibility would enable biotechnological plant managers to swiftly react to volatile markets. In conventional processes, Saccharomyces cerevisiae grows on a relatively limited range of substrates, and produces only a single product—ethanol. Given the observed maturity of the S. cerevisiae fermentation technology, alternatives to baker's yeast may be needed to tip the economic balance in favour of biotechnological ethanol. These alternative fermentation technologies may allow a greater diversity of substrates to be used to produce an individually tailored mix of ethanol and other chemicals. Copyright © 2007 Society of Chemical Industry 相似文献
24.
Sakayu Shimizu Kengo Akimoto Yoshifumi Shinmen Hiroshi Kawashima Michihiro Sugano Hideaki Yamada 《Lipids》1991,26(7):512-516
Incubation with sesame oil increases the mycelial dihomo-γ-linolenic acid content of an arachidonic acid-producing fungus,Mortierella alpina, but decreases its arachidonic acid content [Shimizu, S., K. Akimoto, H. Kawashima, Y. Shinmen and H. Yamada (1989)J. Am. Oil Chem. Soc. 66, 237–241]. The factor causing these effects was isolated and identified to be (+)-sesamin. The results obtained in experiments
with both a cell-free extract of the fungus and with rat liver microsomes demonstrated that (+)-sesamin specifically inhibits
Δ5 desaturase at low concentrations, but does not inhibit Δ6, Δ9 and Δ12 desaturases. Kinetic analysis showed that (+)-sesamin
is a noncompetitive inhibitor (Ki for rat liver Δ5 desaturase, 155 μM). (+)-Sesamolin, (+)-sesaminol and (+)-episesamin, also inhibited only Δ5 desaturases
of the fungus and liver. These results demonstrate that (+)-sesamin and related lignan compounds present in sesame seeds or
its oil are specific inhibitors of Δ5 desaturase in polyunsaturated fatty acid biosynthesis in both microorganisms and animals.
On leave from Suntory Ltd. 相似文献
25.
Md. Majibur Rahman Khan Hideaki Morikawa Mikihiko Miura Yoshie Fujimori Masanobu Nagura 《Carbon》2007,45(5):1035-1042
Carbon fibers were prepared from silk fibers after an iodine treatment and the carbon yield, fiber morphology, structure and mechanical properties were investigated. A single or multi-step carbonization process was used for the preparation. In the single step process, silk fibroin (SF) fibers were heated from 25 to 800 °C with a heating rate of 5 °C min−1 under Ar atmosphere. However, the carbon fiber obtained was partially melted and was too fragile to handle. For better performance, SF fibers were treated with iodine vapor at 100 °C for 12 h and untreated and iodinated SF fibers were heated from 25 to 800 °C by a multi-step carbonization process, which was defined based on the optimum thermal degradation rate of silk. In this multi-step process, the carbon fibers obtained from iodinated SF were structurally intact and stable in appearance, and the carbon yield achieved was ca. 36 wt.%, much higher than the value for untreated SF. X-ray diffraction, Raman spectroscopy and transmission electron microscopic observation revealed that the obtained carbon fibers from both untreated and iodinated SFs had a basically amorphous structure. The strength of carbon fibers prepared from iodinated SF using the multi-step carbonization was considerably increased compared to that of untreated SF. According to viscoelastic measurement, by heating above 280 °C the iodine introduced intermolecular cross-linking of the SF, and its melt flow was inhibited which produced a higher yield and better performance of the carbon fiber. 相似文献
26.
Shimizu Sakayu Akimoto Kengo Kawashima Hiroshi Shinmen Yoshifumi Yamada Hideaki 《Journal of the American Oil Chemists' Society》1989,66(2):237-241
The mycelial dihomo-γ-linolenic acid content of an arachidonic acid-producing fungus,Mortierella alpina 1S-4, was found to increase, with an accompanying marked decrease in its arachidonic acid content, on cultivation with sesame
oil. The resultant mycelia were found to be a rich source of dihomo-γ-linolenic acid. This unique phenomenon was suggested
to be due to specific repression of the conversion of dihomo-γ-linolenic acid to arachidonic acid by the oil. After fractionation
of the oil with acetone into oil and non-oil fractions, it was found that the effective factor(s) was present in the non-oil
fraction. In a study on optimization of the culture conditions for the production of dihomo-γ-linolenic acid byM. alpina 1S-4, a medium containing glucose, yeast extract and the non-oil fraction was found to be suitable for the production. Under
the optimal conditions in a 50-1 fermentor, the fungus produced 107 mg of dihomo-γ-linolenic acid/g dry mycelia (2.17 g/l
of culture broth). This value accounted for 23.1% of the total fatty acids in the lipids extracted from the mycelia. The mycelia
were also rich in arachidonic acid (53.5 mg/g dry mycelia, 11.2%). Other major fatty acids in the lipids were palmitic acid
(24.1%), stearic acid (7.0), oleic acid (20.1), linoleic acid (6.6) and γ-linolenic acid (4.1).
On leave from Suntory Ltd. 相似文献
27.
Silica-supported cobalt catalysts for the selective reduction of nitrogen monoxide with propene 总被引:1,自引:0,他引:1
Megumu Inaba Yoshiaki Kintaichi Masaaki Haneda Hideaki Hamada 《Catalysis Letters》1996,39(3-4):269-274
Catalytic behavior of silica-supported transition metals for NO reduction with propene in the presence of oxygen was investigated. While both silica and cobalt oxides did not show any activity for the selective NO reduction, impregnated CoO/SiO2 prepared from cobalt acetate showed good activity although the preparation conditions had significant effect on the activity. It was suggested that highly dispersed surface Co2+ ions on silica are responsible for the catalytic activity. 相似文献
28.
Hajime Arai Masayuki Tsuda Masahiko Hayashi Hideaki Ohtsuka Yoji Sakurai 《Electrochimica acta》2005,50(9):1821-1828
Several polymorphs of layered nickel dioxide were prepared by using the chemical insertion of alkaline ions into Li0.10NiO2. We used aqueous AOH (A = Li, Na, K) solutions as reducing agents. Sodium and potassium insertion resulted in hydrated layered compounds that can be classified as γ-NiOOH with high crystallinity, while lithium insertion occurred without hydration. We discuss the coordination environment around the A+ ions for these inserted compounds. The thermal behavior, analyzed using high temperature (HT) X-ray diffraction (XRD) and thermogravimetric (TG) measurements, indicated that heating the hydrate at 150 °C yielded its dehydrate. The electrode performance of the nickelate was studied in lithium cells. We discuss the effect of interlayer water on cell rechargeability and the similarity between these nickelate and hydrated manganese dioxide (birnessite). 相似文献
29.
Kojiro Nakai Yasunori Oumi Haruyuki Horie Tsuneji Sano Hideaki Yoshitake 《Microporous and mesoporous materials》2007,100(1-3):328-339
Bromination and subsequent ethylenediamine substitution of the CC double bond in mesoporous ethylenesilica were carried out to explore the characteristics of this periodic mesoporous organosilica. The structures of the products (BrPMO and EDA–BrPMO, respectively) were analysed by IR, Br K-edge EXAFS and NMR spectroscopies, as well as X-ray diffraction and nitrogen adsorption. We showed (1) that the formulae of the two products that formed were [CHBrSiO1.5]0.45[CHSiO1.5]0.55 and [NH2CH2CH2NHCHSiO1.5]0.05 [CHBrSiO1.5]0.40[CHSiO1.5]0.55, respectively, (2) that the addition of Br2 at room temperature occurred on the CC double bonds with disturbing the framework structure, (3) that IR absorption band of CC bonds that reacted with Br2 is significantly different from that of inactive CC bond, (4) that the length of the C–Br bond was considerably longer than in conventional alkyl bromides, and (5) that a large proportion of the ν(C–Br) band remained at the same position in the IR absorption spectrum after the ethylenediamine (EDA) substitution, while a new ν(C–Br) absorption also appeared. The mechanisms of these reactions are discussed at both the micro and mesoscopic levels.
Arsenate adsorption on EDA–BrPMO, in which the EDA is directly bound to the “surface” of the mesopores, was compared with adsorption on EDA–Pr–PMO, which was prepared by the direct synthesis of 3-chloropropyl-functionalized mesoporous ethanesilica followed by the substitution of Cl with EDA. The strength of the adsorption, as measured with the distribution coefficient, was greater for the former adsorbent than the latter. The origin of this difference was attributed to the distance between amino group and the surface. 相似文献
30.
It is of great importance in propene polymerization to control molecular weight and molecular weight distribution as well as isotacticity. Propene polymerization was carried out with an isospecific MgCl2/TiCl4-Cp2TiMe2 catalyst in the presence of various kinds of external Lewis bases. It was found that the molecular weight distribution of the isotactic polymer could be controlled while retaining high activity, high isospecificity and high molecular weight only by changing the kind and/or amount of the Lewis bases. © 1997 Elsevier Science Ltd. 相似文献