Hidehiko Arai
Japan Atomic Energy Research Institute
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Featured researches published by Hidehiko Arai.
Liquid Crystals | 1989
Atsuo Fukuda; Yukio Ouchi; Hidehiko Arai; Hideo Takano; Ken Ishikawa; Hideo Takezoe
Abstract To demonstrate the generality of the chevron structure in ferroelectric liquid crystal (FLC) cells, an optical micrograph is presented, which shows a series of defect lines clearly indicating this structure. The generality is understood as a direct manifestation of the smectic layer undulation playing an important role in the SASC (S*C) phase transition. By establishing the relation between chevrons and asymmetric focal conics, both of which have two senses, ±z, the boundaries between them with opposite senses, i.e. so-called zig-zag defects, have been characterized; the type boundary does not exist as a line but shrinks into a point. The interplay between the chevron structure and the director alignment has been described in detail; in particular, the appearance of unwinding lines in the middle of thick cells, the characterization of internal disclination loops in SSFLC cells, and the law regulating the emission and absorption of internal disclinations by zig-zag defects. With a view to removing...
Applied Radiation and Isotopes | 1993
Masakazu Hosono; Hidehiko Arai; Masaki Aizawa; Ichiro Yamamoto; Ken Shimizu; Masashi Sugiyama
Abstract The electron beam-induced decoloration and degradation of an azo dye (Acid Red 265) in aqueous solution supersaturated with oxygen were studied. The solution, in which the dissolved oxygen concentration (DO) was increased by pressurizing with oxygen gas up to O.3 MPa, was fed through a nozzle to a water channel under atmospheric pressure and irradiated with high-energy electron beams. It was confirmed that with high DO concentration, cleavage of aromatic rings of the dye molecules and reduction of total organic carbon were induced effectively by irradiation. The DO concentration by pressurizing under 0.3 MPa of oxygen was found to be adequate for the electron beam-induced oxidation of organic substances in water in the range of 5–14 kGy.
Radiation Physics and Chemistry | 2000
Koichi Hirota; Teruyuki Hakoda; Hidehiko Arai; Shoji Hashimoto
Abstract To get qualitative and quantitative data for the decomposition of chlorinated hydrocarbons, gaseous chlorobenzene of 10–40 ppm concentrations was irradiated under air condition with electron beam in the dose range of 0–10 kGy. The irradiation decomposed chlorobenzene, and formed gaseous products and aerosols. An irradiation dose of 10 kGy decomposed 80% of chlorobenzene at 10 ppm. Good mass balances on chorine (mgCl) and carbon (mgC) were obtained at doses of 4, 8 and 4 kGy with the addition of NH 3 . About 65% of chlorine in reacted chlorobenzene was dechlorinated by the irradiation at 4 and 8 kGy. The addition of NH 3 enhanced the dechlorination to about 80%. At least about 40% of the gaseous products was found to be aliphatic oxygenates like formate, acetate and α -ketoglutarate at doses of 4 and 8 kGy on the basis of carbon unit (mgC). These aliphatic oxygenates accounted for only 3% in the case of the aerosols. The FTIR analyses revealed that the aerosols consisted of low-vapor-pressured products that had nitrate groups and/or retained the aromatic ring.
Water Research | 1986
Hidehiko Arai; Michimasa Arai; Akihisa Sakumoto
Abstract The combination effect of ionizing radiation and ozone to degrade humic acid in water was superior to ozone and radiation alone. The humic acid treated by this combination method, followed by chlorination, produced only little trihalomethane and total organic halogen. A chain reaction mechanism was suggested for the oxidation of humic acid.
Radiation Physics and Chemistry | 2002
Koichi Hirota; Teruyuki Hakoda; Hidehiko Arai; Shoji Hashimoto
Abstract A study on electron-beam treatment was carried out to find out the effective decomposition conditions of vaporized volatile organic compounds. Air streams containing aromatic and aliphatic compounds were irradiated with electron beams in batch and flow systems. The research showed that chloroethene was readily decomposed through a chain reaction with one of the fragmentation products, Cl radical. A thermal electron and negative oxygen ion were important active species for decomposing carbon tetrachloride. The formation of particles was observed only from the irradiation of aromatics, like benzene, xylene, and chlorobenzene. Dechlorination of chlorobenzene was enhanced in the presence of ammonia.
Radiation Physics and Chemistry | 1981
Hidehiko Arai; Siro Nagai; Koji Matsuda; Motoyoshi Hatada
Abstract The G-values of most products increase with temperature in the radiolysis of methane in a flow-type experiment over the temperature range 50–280°C at atmospheric pressure. The apparent activation energies of most products are higher at higher temperature region above 150°C than those obtained below about 100°C. Irradiation at higher temperature favors the formation of olefins. The results are qualitatively understood on the basis of known nature and reactivity of free radicals.
Applied Radiation and Isotopes | 1997
Agustin N.M. Bagyo; Hidehiko Arai; Teijiro Miyata
Abstract The aqueous solutions of disperse dyes can not be easily decolored and sedimented by γ radiation. The change of pH after irradiation into acidic conditions made sedimentation occur effectively. In oxygen-saturated solutions, absorption band, change of pH and total organic carbon decreased markedly, while in nitrogen-saturated solutions a smooth decrease was seen. Sedimentation was also induced by addition of various electrolytes. The mechanism of the sedimentation was also discussed.
Radiation Physics and Chemistry | 1981
Hidehiko Arai; Siro Nagai; Motoyoshi Hatada
Electron beam irradiation of methane containing small amounts of carbon monoxide in a flow system at atmospheric pressure produced acetic and propionic acids in considerable yields. Propionic acid was formed in preference to acetic acid, especially at small molar ratios, [CO]/[CH4]. These acids were though to be formed via Koch-Haaf reactions CH3++CO→CH3CO+→H2OCH3COOH2+C2H5++CO→C2H5CO+→H2OC2H5COOH2+ The decrease in G(H2) observed by the addition of CO to methane was interpreted on the basis of the following reaction H+CO→k2HCO The estimated values of k2 were close to the reported value.
Radiation Physics and Chemistry | 1980
Siro Nagai; Hidehiko Arai; Motoyoshi Hatada
Abstract Electron beam irradiation of gas mixture of CO and H2 (1:6) in the presence of silica gel exclusively produces carbon dioxide and hydrocarbons in high yields. At the reaction temperature of 140°C, CO2 is preferentially produced, most of which are formed independently of hydrocarbons. The yields of hydrocarbons consisting predominantly of low molecular weight paraffins, obtained at 295°C, were higher by more than an order of magnitude than those by the homogeneous radiolysis and comparable to those by catalytic reactions over Fischer-Tropsch catalyst. Results obtained by irradiation of H2 over silica gel pre-irradiated under COHe gas stream indicate that secondary reactions between H2 and solid deposits produced from CO are responsible for the formation of hydrocarbons in the radiolysis of the COH2 mixture over silica gel.
Radiation Research | 1975
Hidehiko Arai
The self-focusing of a pulsed electron beam in organic gaseous media was investigated as a function of pressure. The relative total ionization cross section of gases, obtained from the present study, is correlated with molar static electron polarization. Below 1 Torr the pinch initially enhances and then declines with increasing pressure. At pressures greater than 10 Torr, the beam exhibits the self-focusing again. The self-focusing between 10 and 40 Torr is successively stronger in gases interacting more strongly with secondary electrons, i.e.,