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71.
A switched reluctance (SR) motor has a doubly salient pole structure. The performance of the SR motor strongly depends on the magnetic properties of the core material, since it consists only of an iron core and copper windings. This study experimentally evaluates the performance of an SR motor made of permendur (Fe–49% Co alloy), which has very high saturation flux density and low core loss. Two types of SR motors that have the same dimensions but different core materials are used: one motor is made of the conventional nonoriented Si steel, and the other is made of permendur. Comparison of the characteristics of the two motors shows that the performance of the permendur SR motor surpasses that of the conventional one in terms of output power and efficiency. © 2014 Wiley Periodicals, Inc. Electr Eng Jpn, 187(1): 51–57, 2014; Published online in Wiley Online Library ( wileyonlinelibrary.com ). DOI 10.1002/eej.22431  相似文献   
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Abstract

Efficient electron-transfer reactions from three kind of tetraselenafulvalenes (TSeF's) to photoexcited triplet state of C60 or C70 in polar solvents have been confirmed by transient absorption spectroscopy observing the decay of 3C60*/3C70* and rise of C60 ??/C70 ??. Growth of single crystal seems to be stimulated by laser irradiation of the solution containing C60 and bis(ethylenedithio)tetraselena-fulvalene (BEDT-TSeF), in which C60 ?? was effectively formed.  相似文献   
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We demonstrate that domain structure of single-layer graphene grown by ambient pressure chemical vapor deposition is strongly dependent on the crystallinity of the Cu catalyst. Low energy electron microscopy analysis reveals that graphene grown using a Cu foil gives small and mis-oriented graphene domains with a number of domain boundaries. On the other hand, no apparent domain boundaries are observed in graphene grown over a heteroepitaxial Cu(111) film deposited on sapphire due to unified orientation of graphene hexagons. The difference in the domain structures is correlated with the difference in the crystal plane and grain structure of the Cu metal. The graphene film grown on the heteroepitaxial Cu film exhibits much higher carrier mobility than that grown on the Cu foil.  相似文献   
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We evaluated the effects of seven mushroom extracts (Grifola frondosa, Pholiota nameko, Panellus serotinus, Hypsizygus marmoreus, Pleurotus cornucopiae, Armillaria mellea, and Flammulina velutipes) on cytotoxic activity and cytokine production of lamina propria leukocytes (LPLs) isolated from rat small (S) and large (L) intestinal mucosa. Boiling water extracts from seven species of mushrooms showed no direct cytotoxicity against the YAC-1 target cells. However, prominent increases of cytotoxicity were observed in S- and L-LPLs co-cultured with P. serotinus extract. Cytokine production (TNFα, IFNγ, IL-12 p70, and IL-4) of S- and L-LPLs was stimulated in response to P. cornucopiae extract. Mushroom extracts contributed to target cell adhesion and/or cytokine production in the effector cells. The promotion of cytotoxic activity in S- and L-LPLs was not necessarily related to β-glucan content of the mushroom.  相似文献   
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β‐Methylglycidyl ethers have been applied to Electrical and Electronic adhesives. However, there is no report about the detailed polymerization behavior and physical properties of their cured products. Hence, we investigated cationic polymerization behavior of bisphenol A di(β‐methylglycidyl) ether (Me‐BADGE) and physical properties of the cured products containing Me‐BADGE. DSC analysis suggested that Me‐BADGE could be cured completely at lower temperature than bisphenol A diglycidyl ether (BADGE). Physical properties were analyzed by dynamic viscoelastic analysis. Glass transition temperature (Tg) of BADGE homopolymer was 194°C. In contrast, the copolymer of BADGE (50 wt %) with Me‐BADGE (50 wt %) showed Tg at 124°C. According to the data of E’ and tan δ, crosslink density of the cured products decreased with increasing the Me‐BADGE content. The analysis of cationic polymerization of monofunctional β‐methylglycidyl ether suggested that the cationic polymerization proceeded not only through oxonium cation but also through carbocation formed by ring‐opening reaction of oxonium cation. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42377.  相似文献   
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