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101.
Alternating current (ac) superconducting machines such as superconducting generators, transformers, or resistive current limiters need large‐current‐capacity conductors. These conductors are generally fabricated as multistrand cables stacked with multifilamentary NbTi superconductors whose current capacity is a few tens of amperes. ac quench current degradation has often been observed in ac use of such multistrand cables. Several reasons for this degradation have been pointed out: nonuniformity of each strand current, mechanical disturbances, thermomagnetic instability, and ac losses. However, it has not as yet been overcome. Since the angle between the strand axis and the cable axis changes along the cable axis in multistrand cables, the strands are exposed to a spatially (axially) distributed magnetic field, which has longitudinal and transverse components changing periodically due to multiple cabling. This paper mainly discusses the thermomagnetic instability due to the distributed transverse magnetic field, which was compared with the self‐field instability and the longitudinal field instability experimentally and theoretically. It was confirmed that the ac quench current degradation due to the distributed transverse field could be induced by the following: nonlinear Ej characteristic, strong dependence of Ej characteristic on magnetic field in low field region, uniformity of the axial current profile inside the superconductor with the high resistive matrix, and the poor thermal diffusion of CuNi/NbTi composites. © 2000 Scripta Technica, Electr Eng Jpn, 131(1): 45–55, 2000  相似文献   
102.
Improved genome editing via oviductal nucleic acids delivery (i-GONAD) is a new technology enabling in situ genome editing of mammalian zygotes exiting the oviductal lumen, which is now available in mice, rats, and hamsters. In this method, CRISPR/Cas9 genome-editing reagents are delivered directly to the oviducts of pregnant animals (corresponding to late zygote stage). After intraoviductal instillation, electric shock to the entire oviduct was provided with a specialized electroporation (EP) device to drive the genome editing reagents into the zygotes present in the oviductal lumen. i-GONAD toward early zygotes has been recognized as difficult, because they are tightly surrounded by a cumulus cell layer, which often hampers effective transfer of nucleic acids to zygotes. However, in vivo EP three min after intraoviductal instillation of the genome-editing reagents enabled genome editing of early zygotes with an efficiency of 70%, which was in contrast with the rate of 18% when in vivo EP was performed immediately after intraoviductal instillation at Day 0.5 of pregnancy (corresponding to 13:00–13:30 p.m. on the day when vaginal plug was recognized after natural mating). We also found that addition of hyaluronidase, an enzyme capable of removing cumulus cells from a zygote, slightly enhanced the efficiency of genome editing in early zygotes. These findings suggest that cumulus cells surrounding a zygote can be a barrier for efficient generation of genome-edited mouse embryos and indicate that a three-minute interval before in vivo EP is effective for achieving i-GONAD-mediated genome editing at the early zygote stage. These results are particularly beneficial for researchers who want to perform genome editing experiments targeting early zygotes.  相似文献   
103.
Fluoroalkyl end‐capped N‐acryloxysuccinimide (ASuI) cooligomers were prepared under very mild conditions by the cooligomerizations of fluoroalkanoyl peroxides with ASuI and comonomers such as N,N‐dimethylacrylamide (DMAA) and acryloylmorpholine (ACMO). These fluorinated ASuI cooligomers thus obtained were in general easily soluble in water and common organic solvents. These fluorinated ASuI cooligomers were also able to reduce the surface tension of water quite effectively to around 20 mN/m with a clear break point resembling a critical micelle concentration (CMC), although the corresponding nonfluorinated ASuI cooligomers were not effective for reducing the surface tension of water. Fluorinated ASuI cooligomers were applicable to new fluorinated precooligomers, and these precooligomers could react with several amino compounds such as aniline, cytosine, and cyclohexylamine to afford fluorinated cooligomer‐bound aromatic and cyclohexyl segments under mild conditions. Of particular interest, these fluorinated precooligomers were able to react with low molecular weight biocides such as sulfathiazole (STZ) and 3‐amino‐5‐hydroxypyrazole (AHP) to give the corresponding fluorinated cooligomers containing antibacterial segments under similar conditions. These cooligomers were shown to have not only a good oleophobicity imparted by fluorine but also surface antibacterial activity against Staphylococcus aureus. Therefore, our present fluorinated cooligomers containing antibacterial segments are suggested to have high potential for new fluorinated functional materials through their surface active property and surface antibacterial activity. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 3874–3880, 2004  相似文献   
104.
A synthesis of Li3V2(PO4)3 being a potential cathode material for lithium ion batteries was attempted via a glass-ceramic processing. A glass with the composition of 37.5Li2O-25V2O5-37.5P2O5 (mol%) was prepared by a melt-quenching method and precursor glass powders were crystallized with/without 10 wt% glucose in N2 or 7%H2/Ar atmosphere. It was found that heat treatments with glucose at 700 °C in 7%H2/Ar can produce well-crystallized Li3V2(PO4)3 in the short time of 30 min. The battery performance measurements revealed that the precursor glass shows the discharge capacity of 14 mAh g−1 at the rate of 1 μA cm−2 and the glass-ceramics with Li3V2(PO4)3 prepared with glucose at 700 °C in 7%H2/Ar show the capacities of 117-126 mAh g−1 (∼96% of the theoretical capacity) which are independent of heat treatment time. The present study proposes that the glass-ceramic processing is a fast synthesizing route for Li3V2(PO4)3 crystals.  相似文献   
105.
An enzyme-synthetic method of demonstrating phosphorylase was applied to the living rabbit cornea, and polyglucose particles synthesized from glucose-1-phosphate in vivo were studied electron microscopically. In the corneas in which the medium for phosphorylase was applied from the anterior chamber or the bulbar subconjunctiva, synthesized polyglucose particles were found in the cytoplasmic matrices of the epithelium. When the medium was deposited in the conjunctival sac, a few synthesized polyglucose particles were found in the cytoplasmic matrices of only the superficial layer of the corneal epithelium. These findings suggest that metabolites for glycogen metabolism come mainly from the aqueous humor in the anterior chamber. The polyglucose particles synthesized by the enzyme-synthetic method in vivo resemble native glycogen particles. In addition, these particles were not overproduced because the synthesis of polyglucose is probably regulated in vivo.  相似文献   
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