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991.
Song J Chen M Olesen MB Wang C Havelund R Li Q Xie E Yang R Bøggild P Wang C Besenbacher F Dong M 《Nanoscale》2011,3(12):4966-4971
Core-sheath silver nanowire/polyvinylpyrrolidone (AgNW/PVP) nanocables have been fabricated via an efficient single-spinneret electrospinning method. The core-sheath structure is revealed by combining several characterization methods. A possible formation mechanism of the AgNW/PVP nanocable involving a strong stretching during the electrospinning process is proposed. Further, electrical measurements were performed on AgNW/PVP nanocables as well as bare AgNWs, which indicated the nanocables became insulating due to the isolation of highly conductive AgNWs by insulating PVP sheath. Therefore, the described fabrication method holds potential for the fabrication of low-cost metal/polymer composite materials for nanoelectronic applications in general. 相似文献
992.
Wei Xie Haifeng ChengZengyong Chu Zhaohui ChenChunguang Long 《Ceramics International》2011,37(6):1947-1951
A series of polyacrylonitrile-based hollow carbon fibres (PAN-HCFs) were prepared by carbonizing polyacrylonitrile (PAN) hollow cured fibres at temperature ranging from 550 to 950 °C for 1 h in nitrogen. The effects of carbonization temperature on the structure, elemental compositions, surface electrical conductivity, electromagnetic parameters and reflectivity of PAN-HCFs were investigated. Results indicate that the obtained PAN-HCFs have not been graphitized and the C content and surface electrical conductivity increases as the carbonization temperature increases. The reflectivity of composites of PAN-HCFs and resin is −7.50 dB at 6.06 GHz and the band of the reflectivity under −5 dB is 6 GHz when the carbonization temperature is 750 °C. 相似文献
993.
In this study, influences of both component ratio of minor phases and charge sequence on the morphology and mechanical performance
in typical ternary blends, polypropylene (PP)/polystyrene (PS)/polyamide-6 (PA6), have been studied. Reactive compatibilization
of the blends has been carried out using multi-monomer melt grafted PP with anhydride groups and styrene segments. For uncompatibilized
blends, scanning electron microscope (SEM) and selective solvent extraction showed that the blends presented a core–shell
morphology with PS as shell and PA6 as core in the PP matrix, in spite of the component ratio and charge sequence. The shell
thickened and droplet size decreased with increasing the PS/PA6 component ratio. While for compatibilized blends, the addition
of compatibilizers resulted in a significant reduction of the dispersed droplet size and the phase structure of the dispersed
phases was greatly dependent on the charge sequence. When the blending of PA6, g-PP, and PP are preceded, the encapsulation
structure reversed into the structure of PS phase encapsulated by PA6 phase, which led to better tensile and flexural strength
of the blends. 相似文献
994.
Anming Wang Fangkai Zhang Feifei Chen Meizhang Wang Haifeng Li Zhaowu Zeng Tian Xie Zhenming Chen 《Korean Journal of Chemical Engineering》2011,28(4):1090-1095
To obtain robust and thermo-stable enzyme aggregates, p-benzoquinone was used as cross-linker and bovine serum albumin (BSA) as crowding macromolecules to prepare cross-linked enzyme aggregates (CLEAs) of lipase. Effects of cross-linking time and cross-linker content on the activity, thermal stability and characteristics of enzyme aggregates were examined carefully. It was observed that when the content of p-benzoquinone was 5 mM and amount of BSA was 125% of that of lipase (w/w), the specific activity of cross-linked co-aggregates of lipase and BSA was 79.8 U mg−1, 2.44-fold of that of cross-linked enzyme aggregates of lipase without BSA. Moreover, after heat treatment for 96 h at 50 °C, the CLEAs prepared with this facile routine kept 75.18% of their initial activity, 5.01-fold more than that of the just CLEAs using glutaraldehyde. Furthermore, BSA macromolecules in lipase CLEAs enhanced the catalytic efficiency of free and just lipase CLEAs without BSA by 1.45 and 2.83 times, respectively. The proposed crosslinking technique would rank among the potential strategies for efficiently preparing robust and thermo-stable enzyme aggregates. 相似文献
995.
996.
Cationic liposomes have emerged as a novel adjuvant and antigen delivery system to enhance vaccine efficacy. However, the role of surface charge density in cationic liposome-regulated immune responses has not yet been elucidated. In the present study, we prepared a series of DOTAP/DOPC cationic liposomes with different surface densities by incorporating varying amounts of DOPC (a neutral lipid) into DOTAP (a cationic lipid). The results showed that DOTAP/DOPC cationic liposome-regulated immune responses relied on the surface charge density, and might occur through ROS signaling. The liposomes with a relatively high charge density, such as DOTAP/DOPC 5:0 and 4:1 liposomes, potently enhanced dendritic cell maturation, ROS generaion, antigen uptake, as well as the production of OVA-specific IgG2a and IFN-γ. In contrast, low-charge liposomes, such as DOTAP/DOPC 1:4 liposome, failed to promote immune responses even at high concentrations, confirming that the immunoregulatory effect of cationic liposomes is mostly attributable to their surface charge density. Moreover, the DOTAP/DOPC 1:4 liposome suppressed anti-OVA antibody responses in vivo. Overall, maintaining an appropriate surface charge is crucial for optimizing the adjuvant effect of cationic liposomes and enhancing the efficacy of liposome-based vaccines. 相似文献
997.
We demonstrate nonvolatile resistive switching in single crystalline ZnO nanowires with high ON/OFF ratios and low threshold voltages. Unlike the mechanism of continuous metal filament formation along grain boundaries in polycrystalline films, the resistive switching in single crystalline ZnO nanowires is speculated to be induced by the formation of a metal island chain on the nanowire surface. Resistive memories based on bottom-up semiconductor nanowires hold potential for next generation ultra-dense nonvolatile memories. 相似文献
998.
The construction and transformation of metal-carbon (M-C) bonds constitute the central themes of organometallic chemistry. Most of the work in this field has focused on traditional M-C bonds involving tetravalent carbon: relatively little attention has been paid to the chemistry of nontraditional metal-carbon (M-C(cage)) bonds, such as carborane cages, in which the carbon is hypervalent. We therefore initiated a research program to study the chemistry of these nontraditional M-C(cage) bonds, with a view toward developing synthetic methodologies for functional carborane derivatives. In this Account, we describe our results in constructing and elucidating the chemistry of transition metal-carboryne complexes. Our work has shown that the M-C(cage) bonds in transition metal-carboranyl complexes are generally inert toward electrophiles, and hence significantly different from traditional M-C bonds. This lack of reactivity can be ascribed to steric effects resulting from the carboranyl moiety. To overcome this steric problem and to activate the nontraditional M-C(cage) bonds, we prepared a series of group 4 and group 10 transition metal-carboryne complexes (where carboryne is 1,2-dehydro-o-carborane), because the formation of metallacyclopropane opens up the coordination sphere and creates ring strain, facilitating the reactions of M-C(cage) bonds with electrophiles. Structural and theoretical studies on metal-carboryne complexes suggest that the bonding interaction between the metal atom and the carboryne unit is best described as a resonance hybrid of the M-C σ and M-C π bonds, similar to that observed in metal-benzyne complexes. The nickel-carboryne complex (η(2)-C(2)B(10)H(10))Ni(PPh(3))(2) can (i) undergo regioselective [2 + 2 + 2] cycloaddition reactions with 2 equiv of alkyne to afford benzocarboranes, (ii) react with 1 equiv of alkene to generate alkenylcarborane coupling products, and (iii) also undergo a three-component [2 + 2 + 2] cyclotrimerization with 1 equiv of activated alkene and 1 equiv of alkyne to give dihydrobenzocarboranes. The reaction of carboryne with alkynes is also catalyzed by Ni species. Subsequently, a Pd/Ni co-catalyzed [2 + 2 + 2] cycloaddition reaction of 1,3-dehydro-o-carborane with 2 equiv of alkyne was developed, leading to the efficient formation of C,B-substituted benzocarboranes in a single process. In contrast, the zirconium-carboryne species, generated in situ from Cp(2)Zr(μ-Cl)(μ-C(2)B(10)H(10))Li(OEt(2))(2), reacts with only 1 equiv of alkyne or polar unsaturated organic substrates (such as carbodiimides, nitriles, and azides) to give monoinsertion metallacycles, even in the presence of excess substrates. The resultant five-membered zirconacyclopentenes, incorporating a carboranyl unit, are an important class of intermediates for the synthesis of a variety of functionalized carboranes. Transmetalation of zirconacyclopentenes with other metals, such as Ni and Cu, was also found to be a very useful tool for various chemical transformations. Studies of metal-carboryne complexes remain a relatively young research area, particularly in comparison to the rich literature of metal-benzyne complexes. Other transition metal-carborynes are expected to be prepared and structurally characterized as the field progresses, and the results detailed here will further that effort by providing easy access to a wide range of functionalized carborane derivatives. 相似文献
999.
1000.