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41.
Enomoto T Kanematsu S Tsunashima K Matsumoto K Hagiwara R 《Physical chemistry chemical physics : PCCP》2011,13(27):12536-12544
Fluorohydrogenate salts of quaternary phosphonium cations with alkyl and methoxy groups (tetraethylphosphonium (P(2222)(+)), triethyl-n-pentylphosphonium (P(2225)(+)), triethyl-n-octylphosphonium (P(2228)(+)), and triethylmethoxymethylphosphonium (P(222(101))(+))) have been synthesized by the metatheses of anhydrous hydrogen fluoride and the corresponding phosphonium bromide or chloride precursors. The three salts with asymmetric cations, P(222m)(FH)(2.1)F (m = 5, 8, and 101), are room temperature ionic liquids (ILs) and are characterized by differential scanning calorimetry, density, viscosity, and conductivity measurements. Linear sweep voltammetry using a glassy carbon working electrode shows these phosphonium fluorohydrogenate ILs have wide electrochemical windows (>4.9 V) with the lowest viscosity and highest conductivity in the known phosphonium-based ILs. Thermogravimetry shows their thermal stabilities are also improved compared to previously reported alkylammonium cation-based fluorohydrogenate salts. Differential scanning calorimetry and X-ray diffraction revealed that tetraethylphosphonium fluorohydrogenate salt, P(2222)(FH)(2)F, exhibits two plastic crystal phases. The high temperature phase has a hexagonal lattice, which is the first example of a plastic crystal phase with an inverse nickel arsenide-type structure, and the low-temperature phase has an orthorhombic lattice. The high-temperature plastic crystal phase exhibits a conductivity of 5 mS cm(-1) at 50 °C, which is the highest value for the neat plastic crystals. 相似文献
42.
Temperature and velocity measurements are performed to clarify the effects of sub-millimeter-bubble injection on the transition
to turbulence in the natural convection boundary layer along a vertical plate in water. In particular, we focus on the relationship
between the bubble injection position L and the transition to turbulence in the natural convection boundary layer. The bubble injection positions used in our experiments
are L = 1.6 and 3.6 mm. Bubble injection at L = 1.6 mm delays the transition to turbulence in the natural convection boundary layer, while that at L = 3.6 mm accelerates the transition to turbulence in the boundary layer. In the case of L = 1.6 mm, the appearance region of the liquid velocity fluctuation in the bubble-induced upward flow in the upstream unheated
section is restricted to near the wall, although the peak of the liquid velocity fluctuation is high. In contrast, in the
case of L = 3.6 mm, the relatively large liquid velocity fluctuation is distributed widely over the laminar boundary layer width. These
results suggest that the effect of the liquid velocity fluctuation on the laminar boundary layer is quite different between
L = 1.6 and 3.6 mm. It is therefore expected that the transition to turbulence in the natural convection boundary layer for
the case with bubble injection is dependent on the magnitude and appearance region of the liquid velocity fluctuation in the
bubble-induced upward flow in the upstream unheated section. 相似文献
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44.
Daisuke Sasaki Yoshihiro Suzuki Hagiwara Toshiki Shoichiro Yano Takashi Sawaguchi 《Journal of Analytical and Applied Pyrolysis》2007,80(2):312-318
The reactive end groups of nonvolatile oligomers obtained by controlled thermal degradation of poly(propylene-ran-ethylene) and poly(propylene-ran-1-butene) were determined by 1H and 13C NMR spectroscopy. The molar ratio of unsaturated to saturated end groups was found to be about 9:1. The average number of unsaturated end groups per molecule was between 1.6 and 1.8, indicating that 60–80 mol% of the oligomer molecules were telechelic, having two terminal unsaturated end groups. These oligomers had a lower polydispersity than the raw material, despite their lower molecular weight and melting temperature. Although the end groups resulting from each monomer unit could be detected by 13C NMR, the end group composition differed from that of the main chains of the raw materials. The end group composition was satisfactorily explained by the differences in bond dissociation energy and activation energy of elementary reactions that occurred during thermal degradation, based on the monomer composition of the raw materials. 相似文献
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Within the framework of perturbative QCD, we investigate the hadroproduction of charmed particles via two-gluon as well as quark-pair annihilation. The total production cross section is found to be sensitive to the choice of the scale parameter Q2 and in general not free from non-perturbative effects. Charmed-particle production in the high-pT region is also studied. 相似文献
48.
Domino Michael reactions of oxophorone and its derivatives 4 with Michael partners 3 have been effected to give bicyclo[2.2.2]octane-2,5-dione derivatives 7 by a catalytic amount of a Brønsted base (NMAP-Li) generated from N-methylaminopropylated silica gel (NMAP) and n-BuLi. The NMAP pellets were efficiently reused up to six times in 86% average yield. 相似文献
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50.
Kaoru Hagiwara 《Physics letters. [Part B]》1979,84(2):241-246
Opposite-side angular distributions of high-pT particles in the jet trigger experiments are studied in the lowest-order QCD. Gluon jets play a crucial role in understanding correlations between two high-pT jets. The angular distribution of the positive-to-negative particle ratio and that of charmed particles can be good probes of the gluon density inside a nucleon. 相似文献