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71.
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
72.
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
73.
Shuji Kodama Atsushi Morikawa Kazuya Nakagomi Atsushi Yamamoto Atsushi Sato Kentaro Suzuki Tomohisa Yamashita Tomoko Kemmei Atsushi Taga 《Electrophoresis》2009,30(2):349-356
Nicotine (NC) and its related compounds (cotinine (CN), nornicotine (NN), anatabine (AT) and anabasine (AB)) were simultaneously enantioseparated by CE using a capillary with amino groups and sulfated β‐CD as a chiral selector. The optimum running conditions were found to be 30 mM acetate buffer (pH 5.0) containing 8% sulfated β‐CD with an applied voltage of +15 kV at 30°C using direct detection at 260 nm. Using a capillary coated with amino groups, the EOF migrates toward the positive pole. However, when sulfated β‐CD was added to the BGE, it was found that the EOF migrated toward the negative pole due to ionic adsorption of sulfated β‐CD to amino groups on the capillary inner wall. All the cationic analytes migrated as anions, suggesting that they formed stable anionic complexes with sulfated β‐CD. With this system and a simple pretreatment with mini‐cartridges, NC alkaloids in five cigarette samples were enantioseparated. As a result, each of the compounds except for CN was detected. In the case of NC, only (S)‐NC was detected (more than 99.9%), but in the case of NN, AT and AB, the ratios of (S)‐isomer to total isomers were in the ranges 58–70, 81–85 and 59–65%, respectively. On the other hand, only NC was detected in cigarette smoke and the ratio of (S)‐ and (R)‐NCs was 96:4. The amounts of NC alkaloids in cigarettes suggest that the production of (R)‐NC resulted from racemization due to the high temperature/burning of the cigarette. 相似文献
74.
Kazuya Uenishi Atsushi Sudo Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2009,47(14):3662-3668
A copolymerization of 10‐methyl‐2H,8H‐benzo‐[1,2‐b:5,4‐b′]bipyran‐2,8‐dione ( 1 ) and glycidyl phenyl ether (GPE) was studied. 1 was a bislactone designed as a bifunctional analogue of 3,4‐dihydrocoumarin (DHCM), of which anionic 1:1 alternating copolymerization with GPE has been reported by us, previously. This alternating nature was inherited by the present copolymerization of 1 and GPE, leading to an intriguing copolymerization behavior in contrast to the ordinary statistical copolymerizations of monofunctional monomers and bifunctional monomers usually controlled by the proportional dependence of the crosslinking density on the monomer feed ratio: (1) When the feed ratio [GPE]0/[ 1 ]0 was 1, the two monomers underwent the 1:1 alternating copolymerization. In this case, 1 behaved as a monofunctional monomer, that is, only one of the two lactones in 1 participated in the copolymerization allowing the other lactone moiety to be introduced into the side chain almost quantitatively. (2) Increasing the feed ratio [GPE]0/[1]0 to larger than 4 allowed almost all of the lactone moieties to participate in the copolymerization system to give the corresponding networked polymers efficiently. The compositions of the copolymers [GPE unit]/[ 1 ‐derived acyclic ester unit] were always biased to smaller values than the feed ratios [GPE]0/[lactone moiety in 1 ]0 by the intrinsic 1:1 alternating nature of the copolymerization. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3662–3668, 2009 相似文献
75.
Hiroki Hotta Kazuya Tatsuno Yoji Hattori Takuya Hashimoto Masayuki Uehara Kin-ichi Tsunoda 《Electrochemistry communications》2008,10(9):1351-1354
The H+ concentration change was monitored near an electrode surface through an electrolysis using a slab optical waveguide technique. Indium tin oxide transparent electrode modified by porous insulating polymer to which methyl red was covalently immobilized was used as a guiding layer, and the absorbance change of the polymer film was monitored. H+ generation at the vicinity of the electrode through the oxidation of ascorbic acid could be monitored by this technique. 相似文献
76.
目前Si基半导体由于其自身材料特性的限制,已经越来越难以满足高速发展的现代电力电子技术对半导体器件的性能要求.SiC作为新一代半导体材料具有显著的性能优势,但由于其属于典型的难加工材料,实现SiC晶圆的高质量与高效率加工成为了推动其产业化应用进程的关键.本综述在回顾近年来SiC超精密加工技术研究进展的基础上,重点介绍了一种基于等离子体氧化改性的SiC高效超精密抛光技术,分析了该技术的材料去除机理、典型装置、改性过程及抛光效果.分析结果表明,该技术具有较高的去除效率,能够获得原子级平坦表面,并且不会产生亚表面损伤.同时针对表面改性辅助抛光技术加工SiC表面过程中出现的台阶现象,探讨了该台阶结构的产生机理及调控策略.最后对等离子体辅助抛光技术的发展与挑战进行了展望. 相似文献
77.
Inagi S Koseki K Hayashi S Fuchigami T 《Langmuir : the ACS journal of surfaces and colloids》2010,26(24):18631-18633
The electrochemical reduction of a fluorene-based conjugated polymer, poly(9-fluorenone-alt-9,9-dioctylfluorene), was investigated for the first time. The carbonyl group in the fluorenone unit was selectively and quantitatively converted to the methylene group, as determined by (1)H NMR, IR, and energy-dispersive X-ray (EDX) analysis. The optical and electrochemical properties of the polymers were studied by UV-vis, photoluminescence (PL), and cyclic voltammetry (CV) measurements and were found to be tunable by varying the reduction level. 相似文献
78.
Yoshiro Kaneko Dr. Kazuya Fujisaki Tsuyoshi Kyutoku Hidemitsu Furukawa Dr. Jun‐ichi Kadokawa Prof. 《化学:亚洲杂志》2010,5(7):1627-1633
In this paper, we describe the preparation of hydrogels through the formation of an inclusion complex of amylose in a vine‐twining polymerization. This is achieved by the phosphorylase‐catalyzed polymerization of α‐D ‐glucose 1‐phosphate from maltoheptaose primer, in the presence of a water‐soluble copolymer having hydrophobic graft‐chains (poly(acrylic acid sodium salt‐graft‐δ‐valerolactone)). The mixture turns into a gel during the polymerization process. Evaluation of the hydrogels is conducted by shear‐viscosity measurements of the products. For the hydrogels with relatively high viscosities, fast relaxation modes of the cooperative diffusions are observed by scanning microscopic light scattering measurements, which indicate the nanometer‐size network structures of the hydrogels. In addition, we found that the enzymatic disruption and reproduction of the hydrogels are achieved by the combination of the amylase‐catalyzed hydrolysis of the amylose component and the formation of amylose by the phosphorylase‐catalyzed polymerization. 相似文献
79.
In this Letter, we investigate the environmental dependence of dark matter halos in theories which attempt to explain the accelerated expansion of the Universe by modifying general relativity (GR). Using high-resolution N-body simulations in f(R) gravity models which recover GR in dense environments by virtue of the chameleon mechanism, we find a significant difference, which depends on the environment, between the lensing and dynamical masses of dark matter halos. This environmental dependence of the halo properties can be used as a smoking gun to test GR observationally. 相似文献
80.
Yoshinao Kumagai Yuuki Enatsu Masanari Ishizuki Yuki Kubota Jumpei Tajima Toru Nagashima Hisashi Murakami Kazuya Takada Akinori Koukitu 《Journal of Crystal Growth》2010,312(18):2530-2536
Void formation at the interface between thick AlN layers and (0 0 0 1) sapphire substrates was investigated to form a predefined separation point of the thick AlN layers for the preparation of freestanding AlN substrates by hydride vapor phase epitaxy (HVPE). By heating 50–200 nm thick intermediate AlN layers above 1400 °C in a gas flow containing H2 and NH3, voids were formed beneath the AlN layers by the decomposition reaction of sapphire with hydrogen diffusing to the interface. The volume of the sapphire decomposed at the interface increased as the temperature and time of the heat treatment was increased and as the thickness of the AlN layer decreased. Thick AlN layers subsequently grown at 1450 °C after the formation of voids beneath the intermediate AlN layer with a thickness of 100 nm or above self-separated from the sapphire substrates during post-growth cooling with the aid of voids. The 79 μm thick freestanding AlN substrate obtained using a 200 nm thick intermediate AlN layer had a flat surface with no pits, high optical transparency at wavelengths above 208.1 nm, and a dislocation density of 1.5×108 cm−2. 相似文献