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991.
In this paper, three kinds of imidazole derivatives, 2-(4-methylphenyl)-4,5-di(2-furyl) imidazole (MDFI), 2-(4-nitrophenyl)-4,5-di(2-furyl) imidazole (NDFI), and 2-(4-tert-butylphenyl)-4,5-di(2-furyl) imidazole (t-BDFI) were synthesized. In an alkaline medium, the chemiluminescence (CL) reaction of imidazole derivatives with H2O2 has been investigated. It was also found that MDFI/H2O2 and t-BDFI/H2O2 systems gave strong CL. When Co2+ was added into the two CL systems, the CL intensity was remarkably enhanced. In the optimum conditions, the CL intensity is linearly related to the logarithm of concentration of Co2+. The linear ranges are 5 × 10−9–2.5 × 10−7 mol/L for MDFI/H2O2 system and 5 × 10−9–2.5 × 10−7 mol/L for t-BDFI/H2O2 system, and the corresponding detection limits are 1.2 × 10−9 mol/L and 1.1 × 10−9 mol/L, respectively. The method was applied to the determination of Co2+ in vitamin B12 injection. Furthermore, the CL mechanism was also discussed.  相似文献   
992.
A new, simple technique has been demonstrated for fabricating high-capacity composite electrode structures. In this technique, Li2MnO3 is leached in acid in the presence of soluble transition metal ions and subsequently annealed between 450 and 850 °C. The technique can be used to prepare a wide variety of composite compounds, in particular, a new family of ‘layered–rocksalt’ xLi2MnO3·(1−x)MO (e.g., M = Ni and Co) structures and modifications thereof, as well as ‘layered–layered’ xLi2MnO3·(1−x)LiMO2 (e.g., M = Mn, Ni, and Co) and ‘layered–spinel’ xLi2MnO3·(1−x)LiM2O4 (e.g., M = Mn and Ni). This novel approach also holds promise for 1) synthesizing materials that reduce the extent of internal phase transitions of composite cathode structures with a high manganese content, and 2) minimizing the extent to which cells need to be electrochemically activated to remove Li2O, thereby reducing the extent of the irreversible capacity loss on the first charge/discharge cycle.  相似文献   
993.
A new porous cobalt hydroxide film has been successfully electrodeposited on nickel foam from 0.1?M cobalt nitrate electrolyte at ?1.0?V vs. SCE without adding any surfactant. The microstructure and surface morphology of prepared cobalt hydroxide films were physically characterized by X-ray diffraction analysis and scanning electron microscopy. The results indicate that an interlaced network structure was obtained. The effects of electrodeposition time, deposition potential, and different substrates on the specific capacitance and microstructure of prepared porous ??-Co(OH)2 thin film were systematically studied. The results indicate that the film deposited on nickel foam at ?1.0?V has excellent electrochemical properties. A maximum specific capacitance of 1473?F?g?1 could be achieved at a current density of 2?A?g?1.  相似文献   
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We report a simple, scalable approach to improve the interfacial characteristics and, thereby, the performance of commonly used polyolefin based battery separators. The nanoparticle-coated separators are synthesized by first plasma treating the membrane in oxygen to create surface anchoring groups followed by immersion into a dispersion of positively charged SiO(2) nanoparticles. The process leads to nanoparticles electrostatically adsorbed not only onto the exterior of the surface but also inside the pores of the membrane. The thickness and depth of the coatings can be fine-tuned by controlling the ζ-potential of the nanoparticles. The membranes show improved wetting to common battery electrolytes such as propylene carbonate. Cells based on the nanoparticle-coated membranes are operable even in a simple mixture of EC/PC. In contrast, an identical cell based on the pristine, untreated membrane fails to be charged even after addition of a surfactant to improve electrolyte wetting. When evaluated in a Li-ion cell using an EC/PC/DEC/VC electrolyte mixture, the nanoparticle-coated separator retains 92% of its charge capacity after 100 cycles compared to 80 and 77% for the plasma only treated and pristine membrane, respectively.  相似文献   
1000.
Kim C  Chung S  Kim YE  Lee KS  Lee SH  Oh KW  Kang JY 《Lab on a chip》2011,11(2):246-252
We present a microfluidic device generating three-dimensional (3D) coaxial flow by the addition of a simple hillock to produce an alginate core-shell microcapsule for the efficient formation of a cell spheroid. A hillock tapered at downstream of the two-dimensional focusing channel enables outside flow to enclose the core flow. The aqueous solution in the core flow was focused and surrounded by 1.8% alginate solution to be solidified as a shell. The double-layered coaxial flow (aqueous phase) was broken up into a droplet by the shear flow of oleic acid (oil phase) containing calcium chloride for the polymerization of the alginate shell. The droplet generated from the laminar coaxial flow maintained a double-layer structure and gelation of the alginate solution made a core-shell microcapsule. The shell-thickness of the microcapsule was adjusted from 8-21 μm by the variation of two aqueous flow rates. The inner shape of the shell was almost spherical when the ratio of the water-glycol mixture in the core flow exceeded 20%. The microcapsule was used to form a spheroid of embryonic carcinoma cells (embryoid body; EB) by injecting a cell suspension into the core flow. The cells inside the microcapsule aggregated into an EB within 2 days and the EB formation rate was more than 80% with strong compaction. The microcapsule formed single spherical EBs without small satellite clusters or a bumpy shape as observed in solid microbeads. The microfluidic chip for encapsulation of cells could generate a number of EBs with high rate of EB formation when compared with the conventional hanging drop method. The core-shell microcapsule generated by 3D focusing in the microchannel was effective in forming large number of spherical cell clusters and the encapsulation of cells in the microcapsule is expected to be useful in the transplantation of islet cells or cancer stem cell enrichment.  相似文献   
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