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1.
The garnet-type fluorides, Na3M2Li3F12 (M = Al, Cr, and Fe) were synthesized as the coprecipitates of ~1 to 10 μm powders from HF solutions. The garnet structures were always obtained under acidic conditions. The incorporation of water molecules into the structure of the Cr and Fe garnets was observed. After heat treatment at 300°C, very small unknown peaks were observed in the X-ray powder pattern in addition to the garnet phase which had a slightly smaller value of the lattice constant than that of hydrous garnets. From the measurement of magnetic properties and Mössbauer effects, the Fe and Cr garnets were found to be paramagnetic with both ions in the trivalent state. Presentation of infrared spectra of the garnets is also included. 相似文献
2.
Horiyama S Suwa K Yamaki M Kataoka H Katagi T Takayama M Takeuchi T 《Chemical & pharmaceutical bulletin》2002,50(7):996-1000
Hydroxylamines gradually undergo oxidation to their oximes on being dissolved in organic solvent (e.g. methanol). This phenomenon was followed by (1)H-NMR and liquid chromatography-mass spectrometry (LC-MS). The oxidation rate was estimated from the peak area observed on the mass chromatogram at the protonated molecule or fragment ion on LC-atmospheric pressure chemical ionization (APCI)-MS. The results showed that the oxidation rate of hydroxylamines depended on the solvent type. 相似文献
3.
Takeshi Suwa Terutaka Watanabe Jiro Okamoto Sueo Machi 《Journal of polymer science. Part A, Polymer chemistry》1978,16(11):2931-2944
The radiation-induced emulsifier-free emulsion polymerization of tetrafluoroethylene was carried out at an initial pressure of 2–25 kg/cm2, temperature of 30–110°C, and under a dose rate of 0.57 × 104?3.0 × 104 rad/hr. The rate of polymerization was shown to be proportional to 1.0 and 1.3 powers of the dose rate and initial pressure, respectively, and is maximal at about 70°C. The molecular weight of polytetrafluoroethylene (PTFE) lies in the range of 105?106, increases with reaction time in the early stage of polymerization, and is maximal at 70°C but is almost independent of the dose rate. An interesting discovery is that PTFE, a hydrophobic polymer, forms as a stable latex in the absence of emulsifier. When PTFE latex coagulates during polymerization under certain conditions, the polymerization rate decreases, probably because polymerization proceeds mainly on the polymer particle surface. The observed rate acceleration and successive increase in polymer molecular weight may be due to slow termination of propagating radicals in the rigid PTFE particles. 相似文献
4.
Hironobu Tahara Yudai Tanaka Shoko Yamamoto Shigeki Yonemori Bun Chan Hiroto Murakami Takamasa Sagara 《Chemical science》2021,12(13):4872
Redox-active ionic liquids (RAILs) are gaining attention as a material that can create a wide range of functions. We herein propose a charge-transfer (CT) RAIL by mixing two RAILs, specifically a carbazole-based ionic liquid ([CzC4ImC1][TFSI]) as a donor and a viologen-based ionic liquid ([C4VC7][TFSI]2) as an acceptor. We investigated the effect of CT interaction on the physicochemical properties of the CT ionic liquid (CT-IL) using the results of temperature-dependent measurements of UV-vis absorption, viscosity, and ionic conductivity as well as cyclic voltammograms. We employed the Walden analysis and the Grunberg–Nissan model to elucidate the effect of the CT interaction on the viscosity and ionic conductivity. The CT interaction reduces the viscosity by reducing the electrostatic attraction between the dicationic viologen and TFSI anion. It also reduces the ionic conductivity by the CT association of the dicationic viologen and carbazole. The electrochemically reversible responses of the viologens in [C4VC7][TFSI]2 and CT-IL are consistent with the Nernstian and the interacting two-redox site models. Notably, the transport and electrochemical properties are modulated by CT interaction, leading to unique features that are not present in individual component ILs. The inclusion of CT interaction in RAILs thus provides a powerful means to expand the scope of functionalized ionic liquids.A redox-active ionic liquid (RAIL) consisting of a carbazole and viologen shows charge transfer (CT) interaction. The physicochemical properties are modulated by the CT interaction by comparison with the individual RAILs. 相似文献
5.
Takeshi Suwa Terutaka Watanabe Jiro Okamoto Sueo Machi 《Journal of polymer science. Part A, Polymer chemistry》1979,17(1):129-138
Simultaneous formation of hydrofluoric acid (HF) in the radiation-induced polymerization of tetrafluoroethylene (TFE) was investigated. HF concentration in PTFE latex was determined mainly by conductometric titration with 0.01 and 0.001N NaOH. The amount of HF formed is almost independent of agitation speed and the amount of n-hexadecane added and is maximal at ca. 70°C corresponding to the rate of polymerization. The rate of HF formation increases with the initial pressure of TFE monomer and dose rate and decreases with polymerization or TFE consumption. This fact suggests that HF is formed mainly by TFE reactions and not by the degradation of PTFE. The mechanism of HF formation in this reaction system in the absence of oxygen is shown in the following two schemes: scheme I is the reaction of TFE with primary radicals (OH·, H·, e) from the radiolysis of water; scheme II is the reaction of water with the species from the radiolysis of TFE. On the assumption that HF is formed only according to scheme I, the G value of HF formation G(HF)calc can be calculated as 11.25. All observed G values G(HF)obs are larger than G(HF)calc. When the polymerization is carried out at 20 kg/cm2 under various dose rates, G(HF)obs increases with the dose rate. When the polymerization is carried out at 3.0 × 104 rad/hr under various pressures, G(HF)obs decreases with the decrease in pressure from 20 to 2 kg/cm2 and is fairly close to G(HG)calc at 2 kg/cm2. This indicates that HF formation is due mainly to scheme II at high pressure (in the presence of enough TFE) and to scheme I as the pressure is lowered. 相似文献
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10.
Hitoshi Watarai Hideaki Monjushiro Satoshi Tsukahara Masayori Suwa Yoshinori Iiguni 《Analytical sciences》2004,20(3):423-434
The recent development of new migration methods of micro-particles in liquids using various external fields is reviewed. The combination of a laser scattering force and a photothermal effect produced photothermal-conversion laser-photophoresis. A dielectric field generated in a planer or a capillary quadrupole electrode realized dielectrophoresis. Using a micrometer-scaled magnetic field gradient, the "Magnetophoretic velocimetry" of micro-particles was invented. Furthermore, the Lorentz force generated by combining an electric field and a magnetic field was utilized for electromagnetophoresis. These new methods were overlooked and the advantages in analytical use were discussed. 相似文献