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81.
Hiroshi Kimura Koichiro Aikawa Yuichi Masubuchi Jun-ichi Takimoto K. Koyama Keiji Minagawa 《Rheologica Acta》1998,37(1):54-60
The mechanism of the electrorheological (ER) effect in two types of liquid crystalline polymer (LCP)/dimethylsiloxane (DMS)
blends was investigated by rheological measurements and by structure observation under electric field and shear flow. The
results show that the phase structures of these immiscible blends can be categorized into slipping (low viscosity) and non-slipping
(high viscosity) states. In the non-slipping state, higher viscosity LCP domains connect the electrodes. In the slipping state,
on the other hand, LCP domains do not connect the electrodes and the shear is mainly confined in the lower viscosity DMS domains.
The ER effect (electrically induced viscosity increase) originates from the electrically induced slipping to non-slipping
transition. In one of the blends, the ER effect occurs only at high shear rate, since this blend is in non-slipping state
even under no field if the shear rate is low.
Received: 29 April 1997 Accepted: 3 November 1997 相似文献
82.
83.
Koichiro DotaTadashi Shimizu Shoji HasegawaMasaaki Miyashita Keiji Tanino 《Tetrahedron letters》2011,52(8):910-912
An efficient method for constructing a 10-membered carbocycle with an oxygen bridge has been developed on the basis of a formal [6+4] cycloaddition reaction. Under the influence of EtAlCl2, a dicobalt hexacarbonyl acetylene complex possessing a benzoyloxy group and an allylsilane moiety reacted with furan to give a 11-oxabicyclo[6.2.1]undec-9-ene derivative. On treatment with iodine, the cycloadduct underwent decomplexation followed by rearrangement of the oxygen bridge to afford a 11-oxabicyclo[5.3.1]undeca-1,5-diene derivative. 相似文献
84.
Sumitomo K Mayumi K Minamikawa H Masuda M Asahi T Shimizu T Ito K Yamaguchi Y 《Electrophoresis》2011,32(3-4):448-454
Although polyethylene oxide (PEO) offers several advantages as a sieving polymer in SDS capillary polymer electrophoresis (SDS-CPE), solution properties of PEO cause deterioration in the electrophoresis because PEO in solution aggregates itself, degrades into smaller pieces, and forms polymer-micelle complexes with SDS. We examined protein separation on SDS-CPE with PEO as a sieving matrix in four individual buffer solutions: Tris-CHES, Tris-Gly, Tris-Tricine, and Tris-HCl buffers. The solution properties of PEO as a sieving matrix in those buffers were examined by dynamic light scattering (DLS) and by surface tension. Preferential SDS adsorption onto PEO disturbed protein-SDS complexation and impaired the protein separation efficiency. Substantial adsorption of SDS to PEO was particularly observed in Tris-Gly buffer. The Tris-CHES buffer prevented SDS from adsorbing onto the PEO. Only Tris-CHES buffer achieved separation of six proteins. This study demonstrated efficient protein separation on SDS-CPE with PEO. 相似文献
85.
Palladium-catalyzed arylative cyclization of propargyl-substituted malonate esters with aryl halides offers a stereoselective approach to alkylidenecyclopropanes. The reaction proceeds by an anti-carbopalladation pathway, which guarantees the exclusive stereocontrol of the resulting double bond. The highly strained as well as densely substituted skeletons of the products facilitate further versatile transformations, which underscores the importance of the products as synthetic intermediates. 相似文献
86.
Guksik Lee Fumito Araoka Ken Ishikawa Yuichi Momoi Osamu Haba Koichiro Yonetake Hideo Takezoe 《Particle & Particle Systems Characterization》2013,30(10):847-852
Ordering transitions are observed in azo‐dendrimer‐dissolved nematic liquid crystal (NLC) droplets dispersed in a glycerol matrix. The dendrimer molecules are spontaneously attached at the interface between NLC and glycerol, so that the nematic directors orient perpendicular to the interface, in the radial configuration. Photoisomerization makes the directors be tangential to the interface, in a photoinduced ordering transition from radial to bipolar structure. Similar experiments are conducted both in cholesteric (Ch) and smectic‐A (SmA) LC droplets. Complicated photoinduced ordering transitions are also observed in Ch and SmA droplets, and the associated molecular orientation changes are discussed. Photoisomerizable azo‐dendrimer molecules provide a possible way to control orientation, even in microdroplet systems in which the interface cannot be treated by conventional surface agents. 相似文献
87.
Hideki Miyaji Takanao Asahi Yoshihisa Miyamoto Kenjiro Asai 《Journal of Polymer Science.Polymer Physics》1987,25(1):159-171
Lattice constants of the monoclinic form of polyethylene under pressures up to 1.8 GPa at 298 K are investigated by x-ray diffraction. The thermal expansion from 100 K to 300 K at atmospheric pressure is also studied. The equation of state is calculated by Pastine's method, taking into account the zero-point vibration, and is compared with experimental results. The calculated results depend largely on the interatomic potential used and the limit of the interatomic distance for summation of the potentials. A change in the angle γ between the a and b axes results in an anisotropic change in the unit cell dimension with both pressure and temperature; the a and b axes change at nearly the same rate. The monoclinic form may have a higher density than the orthorhombic form at pressures above 1.0 GPa. 相似文献
88.
89.
The binding of phenylbutazone (PB) to bovine serum albumin (BSA) was considered to be predominantly due to hydrophobic interaction based on the thermodynamic parameters obtained by an equilibrium dialysis method. Little variation of proton nuclear magnetic resonance (1H-NMR) chemical shift of PB was found with change in the concentration of PB (0.5-5 mM) or upon the addition of BSA (7.25 x 10(-5) M). The NMR spectrum of PB in 0.1 M phosphate buffer solution at pH 7 showed that PB existed as a mesomeric anion. The spin-lattice relaxation time (T1) of PB was almost concentration-independent, but decreased in the presence of BSA to 36-38% for the phenyl group and 48-100% for the butyl group. The spin-spin relaxation time (T2) of PB was also almost independent of concentration, but was remarkably decreased in the presence of BSA to ca. 2.5% for the phenyl group and ca. 6-9% for the butyl group. The ratios of the spin-spin relaxation rate (1/T2) of the free PB to that of the bound PB were ca. 5000-11000 for the butyl group and ca. 23000 for the phenyl group. The binding of PB to BSA was considered to involve primarily the phenyl group. 相似文献
90.
Katsumi Saitoh Koichiro Sera Tadashi Shirai Tatsuji Sato Matsuo Odaka 《Analytical sciences》2003,19(4):525-528
The purpose of this study is to clarify the chemical characterization of PM2.5 and PM10 in diesel exhaust particles (DEP). Sampling of PM2.5 and PM10 in DEP was carried out in November 1999 using an automobile exhaust testing system at the National Traffic Safety and Environment Laboratory, with a diesel truck (engine type: direct injection, displacement: 7,961 cc, carrying weight: 2,020 kg, equivalent inertia weight: 5,600 kg) placed on a chassis dynamometer. Sampling conditions included idling, constant speed of 40 km/h, M-15 test pattern and 60%-revolution/40%-load of maximum power. Samples were collected on a polycarbonate membrane filter (Nuclepore, pore size: 0.8 microm) using a MiniVol Portable Air Sampler (Airmetrics Co., Inc.). The concentrations of several elemental and ionic species in the PM2.5 and PM10 samples were determined by particle induced X-ray emission (PIXE) and ion chromatography analysis. PIXE analysis of the PM2.5 and PM10 samples revealed 15 elements, of which Na, Mg, Si, S, Cl, Ca, Fe and Zn were found to be the major components. Ionic species were Cl-, NO2-, NO3-, SO4(2-), Na+, NH4+, K+ and Ca2+. Concentrations of elements and ionic species under the sampling condition of 60%-revolution/40%-load were highest in comparison with those of the other sampling conditions. The elemental and ionic species data were compared for PM2.5 and PM10; PM2.5 concentrations were 70% or more of PM10 concentrations for the majority of elements, and concentrations of ionic species in PM2.5 and PM10 were almost identical. 相似文献