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排序方式: 共有2002条查询结果,搜索用时 15 毫秒
31.
Xian Wang Hiroyuki Hirano Toshio Tagawa Hiroyuki Ozoe 《Chemical Engineering Communications》2007,194(6):835-848
Water mist (diamagnetic) flow in a superconducting magnet of 10 T at various angles is studied experimentally and numerically. Water mist is produced by ultrasonic atomizers and fed into a cylindrical Plexiglas pipe (inner diameter, 90 mm) placed in a bore space of an inclined superconducting magnet. The water mist is found to stop at some locations in the magnet at inclined angles ψ ≤ π/6. At ψ ≥ π/4, the amount of mist flowing out of the other opening of the pipe increases with an increase in inclined angle. In the computation of this phenomenon, water mist is simulated with 1000 water droplets of 3 μm diameter. Brownian motion is considered and the Langevin equation is solved. The numerical results show that at ψ ≤ π/6, most of the water droplets accumulate above the magnetic coil. However, at ψ ≥ π/4, with an increase in inclined angle, the number of water droplets passing through the magnetic coil increases. 相似文献
32.
Effects of hydrostatic extrusion on the thermal properties of polycarbonate (PC) and of high-impact polystyrene (HIPS) were studied using differential scanning calorimeter (DSC) measurements. A glass transition temperature (Tg) and a peak temperature were determined from the DSC curves for both PC and HIPS extrudates. The Tg values of the PC extrudates, with a percentage reduction in area, R, from 40 to 50%, change appreciably from the value for the as–received PC. The results of the hydrostatic extrusion of the PC billets suggest that a two stage deformation process of molecular chains may be involved. Shear-banding is observed for HIPS extrudates with R = 30 to 60%; this fact indicates that a sub-glass transition (β-transition) occurs at temperatures below Tg. It is suggested that the molecular chains of the HIPS extrudate with R = 70% are oriented in the direction of hydrostatic extrusion. The deformation mechanism of molecular chains caused by the hydrostatic extrusion is discussed. 相似文献
33.
Yoshitsugu Kojima Takashi Ohta Mitsumasa Matsushita Minoru Takahara Toshio Kurauchi 《Polymer Engineering and Science》1992,32(10):686-689
Flat packages (FPs) were formed from epoxy molding compounds with various physical properties using a transfer molding machine. The compounds were prepared by changing kinds and amounts of additives and addition methods. The thermal shock test was carried out by the following procedures. The plastic package was soaked alternately in liquid nitrogen (?196°) and in liquid solder (200°) in the cycle of 140s. The median life to crack initiation was defined to be the cycles when half of the specimens exhibited crack initiation. According to linear fracture mechanics, the following expression was obtained relating the median life N, thermal stress σt, and strength σb; N = C/σ·(σb/σt)m. We found the linear relation between logarithm of Nσ and logarithm of σb/σt for various packages, and estimated the values of C and m as 5 × 104 MPa2 and 5.5, respectively. The value of m was the same as that obtained for a dual-in-line package. 相似文献
34.
Naoto Kimbara Akio Nishijima Toshio Sato Yuji Yoshimura Hiromichi Shimada Nobuyuki Matsubayashi Akinori Yukimura 《Catalysis Letters》1990,6(3-6):409-415
TiN supported molybdenum sulfide catalysts showed much higher activity for cleavage of C-C bonds than oxide supported molybdenum sulfide catalysts, indicating the possibility of a new generation of supports for hydroprocessing catalysts. 相似文献
35.
Toshio Kimura Yoshikatu Okada Takashi Yamaguchi Yuzo Shimada Kazuaki Utsumi 《The Journal of Adhesion》1994,47(1):179-190
Bondability and interfacial reaction between dielectric and insulator layers have been examined to obtain a basic understanding of bonding mechanisms. Lead-containing complex perovskite was used as a dielectric material. Two kinds of glass-ceramics were used as insulator material; lead borosilicate glass containing Al2O3 (insulator A) and the same containing Al2O3 and MgO (insulator B). Dielectric and insulator layers did not bond when insulator A was used. When insulator B was used, however, strong bonding was achieved between the two layers by firing the powder compacts at temperatures between 800° and 1000°C. Addition of MgO to lead borosilicate glass increased the thermal expansion coefficient to that of the dielectric and enhanced the formation of reaction layers, resulting in good bonding. Two reaction layers were identified. The main reaction products were enstatite and bredigite for one layer contacting the dielectric, and enstatite and a compound with the same diffraction pattern as that of faujasite for the other layers contacting insulator B. 相似文献
36.
Chengzhi Hu Masahiro Nakajima Tao Yue Masaru Takeuchi Minoru Seki Qiang Huang Toshio Fukuda 《Microfluidics and nanofluidics》2014,17(3):457-468
Alginate hydrogel has widespread applications in tissue engineering, cancer therapy, wound management and drug/cell/growth factor delivery due to its biocompatibility, hydrated environment and desirable viscoelastic properties. However, the lack of controllability is still an obstacle for utilizing it in the fabrication of 3D tissue constructs and accurate targeting in mass delivery. Here, we proposed a new method for achieving magnetic alginate hydrogel microfibers by dispersing magnetic nanoparticles in alginate solution and solidifying the magnetic alginate into hydrogel fiber inside microfluidic devices. The microfluidic devices have multilayered pneumatic microvalves with hemicylindrical channels to fully stop the fluids. In the experiments, the magnetic nanoparticles and the alginate solution were mixed and formed a uniform suspension. No aggregation of magnetic nanoparticles was found, which is crucial for flow control inside microfluidic devices. By regulating the flow rates of different solutions with the microvalves inside the microfluidic device, magnetic hydrogel fibers and nonmagnetic hydrogel fibers were fabricated with controlled sizes. The proposed method for fabricating magnetic hydrogel fiber holds great potential for engineering 3D tissue constructs with complex architectures and active drug release. 相似文献
37.
In the copolymerization of phenylacetylene with various acetylenes catalysed by WCl6·Ph4Sn, the relative reactivity of monomer decreased with increasing steric effect of monomer, e.g. HC Cn-Bu, HC Cn-Hex > HC CPh, HC Cs-Bu > HC Ct-Bu, MeCCPh, CICCPh. While 1-chloro-2-phenylacetylene (a disubstituted acetylene) showed high reactivity in the homopolymerization by Mobased catalysts, the reactivity was remarkably depressed in the presence of phenylacetylene as comonomer. Based on these results, the relative reactivity of the acetylenic monomers in copolymerization was explained in terms of competitive coordination of monomers to the propagating end. 相似文献
38.
Studies are reported of the effect of an essential fatty acid (EFA) deficiency on synthesis of triglycerides (TG) and phospholipids
(PL) and secretion of these compounds by livers of male Sprague-Dawley rats. Animals were fed a semipurified diet containing
corn oil or hydrogenated coconut oil (HCO) as the sole source of fat or no fat from weaning to 20 weeks of age. Liver function
of the animals in each group was compared by an isolated liver perfusion technique with perfusates containing erythrocytes
and linoleate, and in vivo experiments via tail vein injection of palmitate-3H. Perfusion experiments showed that an EFA deficiency reduced the ability of the liver to secrete TG and PL. Accumulation
of TG in the liver and its diminished secretion into the blood of EFA deficient animals were demonstrated by in vivo experiments
with palmitate-3H. The rate of conversion of linoleate to arachidonate and synthesis of PL was greater in livers of EFA deficient rats than
in the control, corn oil fed animals. The results suggest a relationship of EFA metabolism to lipid transport.
One of five papers to be published from the Symposium “Lipid Transport” presented at the AOCS Meeting, New Orleans, April
1970. 相似文献
39.
According to Bikerman, who attributes failure in adhints to a weak boundary layer, it is almost impossible and meaningless to correlate adhesive strength to surface-chemical properties of adhints. Though his assertion seems to be confirmed by the recent studies of Schonhorn and his coworkers on the methods of CASING and TCR, not a few results have yet been accumulated, which show a close relation between them. In this paper surface-chemical criteria for the optimum adhesion are investigated and the minimum interfacial tension or the maximum wetting pressure is deduced from the published data and our own as a first approximation. It is emphasized that, when critical surface tension γc would be used as a measure of surface-chemical properties of solid, its variability according to liquid series (nonpolar, polar and hydrogen bonding liquids) should be carefully taken into consideration. The importance is shown for polyethylene and its fluorine substituted polymers, using newly measured contact angle data and Zisman's data. Results of Levine et al. and Schonhorn et al. on adhesive shear strength with epoxy adhesives are replotted against available values of γc obtained by the use of hydrogen bonding liquid (γcc), which are thought to reflect wetting behaviors of epoxy adhesives quite well. Each curve shows a maximum around γcc = 40 dyne/cm with few points falling off the curves. 相似文献
40.
The subsequent melting behaviour of poly(butylene succinate) (PBSU) and poly(ethylene succinate) (PES) was investigated using DSC and temperature modulated DSC (TMDSC) after they finished nonisothermal crystallization from the melt. PBSU exhibited two melting endotherms in the DSC traces upon heating to the melt, which was ascribed to the melting and recrystallization mechanism. However, one melting endotherm with one shoulder and one crystallization exotherm just prior to the melting endotherm were found for PES. The crystallization exotherm was ascribed to the recrystallization of the melt of the crystallites with low thermal stability, and the shoulder was considered to be the melting endotherm of the crystallites with high thermal stability. The final melting endotherm was ascribed to the melting of the crystallites formed through the reorganization of the crystallites with high thermal stability during the DSC heating process. TMDSC experiments gave the direct evidences to support the proposed models to explain the melting behaviour of PBSU and PES crystallized nonisothermally from the melt. 相似文献