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81.
Masahiro Tajima Miki Niwa Yasushi Fujii Yutaka Koinuma Reiji Aizawa Satoshi Kushiyama Satoru Kobayashi Koichi Mizuno Hideo Ohuˆchi 《Applied catalysis. B, Environmental》1997,12(4):1418
The decomposition of chlorofluorocarbons (CFCs) in the presence of water was examined over a variety of solid acid catalysts. The TiO2ZrO2 catalyst was found to have the highest activity and longest life among the catalysts examined. The activity of the TiO2ZrO2 catalysts depended upon the content of TiO2. At the contents of TiO2 from 58 to 90 mole%, the TiO2ZrO2 catalysts exhibited high activity, and these catalysts were proven to contain TiZrO4 crystal. From the study of the XRD peak intensity of the TiZrO4 crystal, it was highest on the TZ-58 which contained 58 mole% of TiO2, and decreased with increasing the content of TiO2. Furthermore, the conversion of CFC113 measured at 673 K was highest at TZ-58, and decreased gradually with increasing TiO2 content. Therefore, the TiZrO4 crystal influences the activity of decomposition of CFC113. However, the TiO2ZrO2 catalyst was gradually deactivated during the reaction due to the elimination of titanium atoms. A good relationship was found between the activity on TiO2ZrO2 catalyst and bond energy of CCl in the compounds of chlorofluorocarbons and hydrochlorocarbons, suggesting that the rate controlling step was the cleavage of CCl bond. 相似文献
82.
Minoru Kobayashi 《应用聚合物科学杂志》1988,35(2):311-319
The effects of sequence distribution on the glass transition temperature (Tg) of the title terpolymers prepared by radical polymerization were studied. Tg was examined by thermomechanical analysis. The average diad concentrations, as estimation of sequence distributions were calculated from monomer reactivity ratios. A modified Gibbs–Dimarzio equation for binary copolymers was extended to terpolymers to explain the relation between observed Tg and average diad concentrations. The observed Tg showed good agreement with the calculated values determined by the extended equation. 相似文献
83.
Pyrolytic carbon was deposited from acetylene in a fluidized bed at 1100°C on alumina microspheres. In case when only argon was used as the diluent gas, density and BAF of the deposit decreased and deposition yield increased with increasing acetylene concentration. Hydrogen sypply suppressed carbon formation and, consequently, caused an increase in density and Lc. BAF was relatively independent of hydrogen concentration. It was found that high density, isotropic carbon can be deposited from acetylene at 1100°C, if an appropriate proportion of hydrogen is added. 相似文献
84.
This study was undertaken to elucidate the state of a polymer in the amorphous state through a change of motion of the molecular chain caused by heat treatment below the glass transition temperature. From dielectric measurements of amorphous poly(ethylene terephthalate) heat-treated below Tg, it was found that the average relaxation time, the distribution of relaxation time and the dielectric strength increase with increase of heat treatment. From these results, it was concluded that the amorphous state becomes more random by heat treatment. 相似文献
85.
Hideto Matsuyama Kentarou Hayashi Taisuke Maki Masaaki Teramoto Noboru Kubota 《应用聚合物科学杂志》2004,93(1):471-474
Microporous high‐density polyethylene (HDPE) and low‐density polyethylene (LDPE) hollow fiber membranes were prepared from polyethylene–diisodecyl phthalate solution via thermally induced phase separation. Effect of the polyethylene density on the membrane structure and performance was investigated. The HDPE membrane showed about five times higher water permeability than the LDPE membrane because it had the larger pore and the higher porosity at the outer membrane surface. The formation of the larger pore was owing to both the initial larger structure formed by spinodal decomposition and the suppression of the diluent evaporation from the outer membrane surface due to the higher solution viscosity. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 471–474, 2004 相似文献
86.
Phase separation rate during porous membrane formation by immersion precipitation was investigated by light scattering in a polyimide/N‐Methylpyrrolidone (NMP)/water system. In the light scattering measurement, plots of scattered intensity against scattered angle showed maxima in all cases, which indicated that phase separation occurred by a spinodal decomposition (SD). Characteristic properties of the early stage of SD, such as an apparent diffusion coefficient Dapp and an interphase periodic distance Λ, were obtained. The growth process of Λ was also followed by light scattering. The growth rate had the same tendency as Dapp when water content in the nonsolvent bath and the polymer concentration in the cast solution were changed. The pore size of the final membrane increased with decreasing water content, which was opposite to the tendency of Λ growth rate. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 292–296, 2003 相似文献
87.
The chemical reactivities of novel reactive antioxidants based on tetrazoles for carbon–carbon double bonds of liquid polybutadiene and their antioxidation activities toward isoprene rubber were evaluated. These antioxidants, i.e., 2-substituted phenyl-5-(3′,5′ -di-tert-butyl-4′-hydroxyphenyl)tetrazoles (PHPT), were pyrolyzed in liquid polybutadiene at 160–170°C for 30 min to attach to rubber in extents of 61–85% of the nitrileimines formed from PHPT by 1,3-dipolar addition reaction. The reactivities of PHPT followed the order p-Cl > m-Cl > H > p-CH3 > m-CH3, p-OC2H5, suggesting that PHPT reacts with diene rubber in electrophilic reaction and p-derivatives exhibit higher contents of binding than m-derivatives due to steric hindrance. From oxygen absorption data, the antioxidation activities of PHPT for isoprene rubber vulcanizates followed the order m-Cl, m-CH3 > H, p-Cl, p-Cl, p-CH3 > p-OC2H5. Isoprene rubber vulcanizates, obtained after pretreatment with PHPT by heating, were extracted with acetone, followed by aging to show that there was good retention and appreciable antioxidation activities of PHPT, especially, p-CH3 and p-Cl substituted PHPT. 相似文献
88.
Fumiaki Kobayashi Toru Ogawa Mitsuo Akabori Yoshio Kato 《Journal of the American Ceramic Society》1995,78(8):2279-2281
Uranium-plutonium nitride is a candidate fuel for fast reactors, but its major drawback is 14 C formation from natural nitrogen. One would probably have to use highly 15 N-enriched nitrogen. A pyrochemical process with molten-salt electroreflning has been proposed as a means to increase the nuclear proliferation resistance of the fuel cycle. Molten-salt electroreflning could also be applied to nitride fuels to make possible the recycling of 15 N. The anodic dissolution behavior of UN in LiCI-KCI melt was studied to provide the basis for a feasibility study of electroreflning of irradiated nitride fuels. 相似文献
89.
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
90.
We have developed a new multicolor holographic polymer film. Our holographic polymer film contains 3‐[(2,4,6‐trichloro)azo]‐9H‐carbazole‐9‐ethanol (A‐1) and poly(methyl methacrylate). The holographic polymer film can be recorded with a holographic image without applying an external electric field. The diffraction efficiency was 57% at A‐1 with a 20 wt% of dope ratio. The writable holographic image writing for the holographic polymer film step used the silver halide photographic emulsion master plate 532‐nm laser beam under the nonelectric field. After the copy hologram is formed, our holographic polymer film can be displayed in red and green holographic images. Even though our holographic polymer film is rewritten over 200 times, the diffraction efficiency does not fall. As the holographic polymer film is manufactured using roll‐to‐roll techniques, although still in a laboratory scale in this study, it has a strong possibility of being manufactured in larger sizes with lower cost. 相似文献