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排序方式: 共有178条查询结果,搜索用时 125 毫秒
111.
Masahiro Tanaka Hiromi Kato Naoyuki Suzuki Chie Iwata Naofumi Akata 《Journal of Radioanalytical and Nuclear Chemistry》2018,318(2):877-885
A water bubbler system that can distinguish chemical forms of tritium was proposed for long-term tritium monitoring of the exhaust gas of a large fusion test device. The characteristics and performance of the water bubbler system were evaluated under operational conditions and confirmed to be suitable for tritium monitoring. For the tritium measurements, the water bubbler system determined the tritium activity and distinguished the chemical forms of tritium. The tritium activity and chemical forms in the exhaust gas provided helpful information to understand the tritium behavior in the large fusion test device. 相似文献
112.
Naofumi Naga Hitomi Nagino Midori Iwashita Tomoharu Miyanaga Hidemitsu Furukawa 《Journal of polymer science. Part A, Polymer chemistry》2015,53(11):1360-1368
Organic–inorganic hybrid gels containing Si‐vinylene units have been synthesized by a hydrosilylation reaction of tri‐ or tetra‐ethynyl aryl compounds, 1,3,5‐triethynylbenzene (TEB), 3,3′,5,5′‐tetraethynylbiphenyl (TEBP), or tetrakis(4‐ethynylphenyl)methane (TEPM), and bisdimethylsilyl compounds, 1,1,3,3‐tetramethyldisiloxane (TMDS) or 1,4‐bisdimetylsilylbenzene (BDMSB), in toluene. Network structure of the resulting gels was quantitatively characterized by a scanning microscopic light scattering. The reactions yielded the gels having homogeneous network structure of 1.5–2.9 nm mesh size under the monomer concentrations that were relatively higher than the critical gelation concentration. The gels obtained from TEB showed broad absorption in the range from 340 to 370 nm, and emission in the range from 440 to 490 nm. The TEB–BDMSB gels showed remarkable red shift of the emission in comparison with that of the corresponding reaction solutions derived from the network formed by σ–π conjugation. The TEPM–TMDS, BDMSB gels exited by 280 nm showed not only the emission peak at around 360 nm derived from TEPM, but the broad peak at around 420 nm, which should be derived from interaction between phenyl groups of TEPM in the gels. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 1360–1368 相似文献
113.
Dinuclear palladium complexes catalyzed addition reactions of carboxylic acid O-H bond to unactivated internal alkynes. The reaction afforded a trans-adduct selectively. 相似文献
114.
Minoru Tanabe Hiroaki Nishimura Naofumi Ohnishi Kevin B. Fournier Shinsuke Fujioka Atsushi Iwamae Stephanie B. Hansen Keiji Nagai Frederic Girard Michel Primout Bruno Villette Didier Brebion Kunioki Mima 《High Energy Density Physics》2010,6(1):89-94
The propagation of a laser-driven heat-wave into a Ti-doped aerogel target was investigated. The temporal evolution of the electron temperature was derived by means of Ti K-shell X-ray spectroscopy, and compared with two-dimensional radiation hydrodynamic simulations. Reasonable agreement was obtained in the early stage of the heat-wave propagation. In the later phase, laser absorption, the propagation of the heat-wave, and hydrodynamic motion interact in a complex manner, and the plasma is mostly re-heated by collision and stagnation at the target central axis. 相似文献
115.
Naofumi Naga Yukio Imanishi 《Journal of polymer science. Part A, Polymer chemistry》2003,41(3):441-448
Copolymerization of ethylene or propylene and norbornene (NB) was carried out with stereospecific zirconocene catalysts rac‐ethylenebis(indenyl)zirconium dichloride, rac‐dimethylsilylenebis(indenyl)zirconium dichloride ( 2 ), rac‐dimethylsilylenebis(2‐methylindenyl)zirconium dichloride, and diphenylmethylene(cyclopentadienyl)(9‐fluorenyl)zirconium dichloride combined with cocatalysts at 40 °C. Temperature‐rising elution fractionation of the copolymers was carried out with cross‐fractionation chromatography with o‐dichlorobenzene as a solvent, and a broad distribution of the copolymer composition was detected. The fraction eluted at lower temperature contained higher NB. The effect of the polymerization time was examined in the ethylene–NB copolymerization with catalyst 2 , and the higher‐temperature elution fraction increased with increasing polymerization time. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 441–448, 2003 相似文献
116.
The surface reaction on titanium due to pulsed Nd:YAG laser irradiation in a nitrogen atmosphere was investigated using X-ray photoelectron spectroscopy (XPS). The laser, with a wavelength of 532 nm (SHG mode), was irradiated on a titanium substrate in an atmosphere-controlled chamber, and then the substrate was transported to an XPS analysis chamber without exposure to air. This in situ XPS technique makes it possible to clearly observe the intrinsic surface reaction. The characteristics of the surface layer strongly depend on the nitrogen gas pressure. When the pressure is 133 kPa, an oxynitride and a stoichiometric titanium nitride form the topmost and lower surface layers on the titanium substrate, respectively. However, only a nonstoichiometric titanium oxide layer containing a small amount of nitrogen is formed when the pressure is lower than 13.3 kPa. Repetition of laser shots promotes the formation of the oxide layer, but the formation is completed within a few laser shots. After the initial structure is formed, the chemical state of the surface layer is less influenced by the repetition of laser shots. 相似文献
117.
118.
The Suzuki? Miyaura coupling reaction catalyzed by dinuclear palladium complexes gave cine‐substitution products along with ordinary ipso‐substitution products. In the reaction in (D6)benzene, the ipso position of the cine‐substitution product was highly deuterated. The H/D exchange also occurred in various positions of benzene rings. 相似文献
119.
Ayako Ishii Naofumi Ohnishi Hiroki Nagakura Hirotaka Ito Shoichi Yamada 《High Energy Density Physics》2013,9(2):280-287
We present numerical attempts of radiative transfer in a relativistic scattering flow that can produce gamma rays using a three-dimensional Monte Carlo code. We prepared an initial background flowfield obtained from hydrodynamical simulation of a relativistic jet in which Thomson scattering dominates compared to absorption, and solved the radiative transfer equation for the background evolved by a simple expansion model. Since a large number of sample particles is required for an accurate computation, we have parallelized the Monte Carlo code in order to obtain solutions in a practical computational time even for a long-term simulation coupled with a time-dependent flowfield. Using this code, higher parallel efficiency is achieved with larger number of particles. The obtained light curve from the simple model shows a signal of the transition from the opaque post-shock flow to the transparent regime as the flow expands, and the high-energy photons are generated by not only the Doppler boosting but also the inverse Compton scattering. 相似文献
120.
Naofumi Naga 《Journal of polymer science. Part A, Polymer chemistry》2005,43(6):1285-1291
The copolymerization of ethylene and cycloolefins [cyclopentene (CPE), cyclohexene (CHX), cycloheptene (CHP), cyclooctene (COT), cyclododecene (CDO), norbornene (NB), and 5,6‐dihydrodicyclopentadiene HDCPD] and cyclodiolefins [1,3‐cyclopentadiene (CPD), 1,4‐cyclohexadiene (CHD), 1,5‐cyclooctadiene (COD), 2,5‐norbornadiene (NBD), and dicyclopentadiene (DCPD)] was investigated with a constrained‐geometry catalyst, dimethylsilylene(tetramethylcyclopentadienyl)(N‐tert‐butyl)titanium dichloride, with methyl isobutyl aluminoxane as a cocatalyst. In the copolymerization with cycloolefins, the olefins, except for CHX, CDO, and HDCPD, were copolymerized via the 1,2‐insertion mode with the following reactivity: NB > CHP > COT > CPE. In the copolymerization with cyclodiolefins, corresponding copolymers, except for copolymerization with CHD, were obtained. A crosslinking fraction was detected in the copolymers with COD and NBD. The reactivity of the cyclodiolefins, except for COD, was higher than that of the cycloolefins. CPD was copolymerized via 1,2‐insertion, 1,4‐insertion or 1,2‐insertion of dimerized DCPD. The copolymerization with COD showed peculiar behavior under the copolymerization condition of a high COD concentration in the feed. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1285–1291, 2005 相似文献