A 3D flower‐like mesoporous Ni@C composite material has been synthesized by using a facile and economical one‐pot hydrothermal method. This unique 3D flower‐like Ni@C composite, which exhibited a high surface area (522.4 m2 g?1), consisted of highly dispersed Ni nanoparticles on mesoporous carbon flakes. The effect of calcination temperature on the electrochemical performance of the Ni@C composite was systematically investigated. The optimized material (Ni@C 700) displayed high specific capacity (1306 F g?1 at 2 A g?1) and excellent cycling performance (96.7 % retention after 5000 cycles). Furthermore, an asymmetric supercapacitor (ASC) that contained Ni@C 700 as cathode and mesoporous carbon (MC) as anode demonstrated high energy density (60.4 W h kg?1 at a power density of 750 W kg?1). 相似文献
To determinate the water diffusion coefficients and dynamics in adhesive/carbon fiber reinforced epoxy resin composite joints,energy dispersive X-ray spectroscopy analysis(EDX)is used to establish the content change of oxygen in the adhesive in adhesive/carbon fiber reinforced epoxy resin composite joints.As water is made up of oxygen and hydrogen,the water diffusion coefficients and dynamics in adhesive/carbon fiber reinforced epoxy resin composite joints can be obtained from the change in the content of oxygen in the adhesive during humidity aging,via EDX analysis.The authors have calculated the water diffusion coefficients and dynamics in the adhesive/carbon fiber reinforced epoxy resin composite joints with the aid of both energy dispersive X-ray spectroscopy and elemental analysis.The determined results with EDX analysis are almost the same as those determined with elemental analysis and the results also show that the durability of the adhesive/carbon fiber reinforced epoxy resin composite joints subjected to silane coupling agent treatment is better than those subjected to sand paper burnishing treatment and chemical oxidation treatment. 相似文献
Graphene oxide (GO) was functionalized using three different diamines, namely ethylenediamine (EDA), 4,4′-diaminodiphenyl sulfone (DDS) and p-phenylenediamine (PPD) to reinforce an epoxy adhesive, with the aim of improving the bonding strength of carbon fiber/epoxy composite. The chemical structure of the functionalized GO (FGO) nanosheets was characterized by elemental analysis, FT-IR and XRD. Hand lay-up, as a simple method, was applied for 3-ply composite fabrication. In the sample preparation, the fiber-to-resin ratio of 40:60 (w:w) and fiber orientations of 0°, 90°, and 0° were used. The GO and FGO nanoparticles were first dispersed in the epoxy resin, and then the GO and FGO reinforced epoxy (GO- or FGO-epoxy) were directly introduced into the carbon fiber layers to improve the mechanical properties. The GO and FGO contents varied in the range of 0.1–0.5 wt%. Results showed that the mechanical properties, in terms of tensile and flexural properties, were mainly dependent on the type of GO functionalization followed by the percentage of modified GO. As a result, both the tensile and flexural strengths are effectively enhanced by the FGOs addition. The tensile and flexural moduli are also increased by the FGO filling in the epoxy resin due to the excellent elastic modulus of FGO. The optimal FGO content for effectively improving the overall composite mechanical performance was found to be 0.3 wt%. Scanning electron microscopy (SEM) revealed that the failure mechanism of carbon fibers pulled out from the epoxy matrix contributed to the enhancement of the mechanical performance of the epoxy. These results show that diamine FGOs can strengthen the interfacial bonding between the carbon fibers and the epoxy adhesive. 相似文献
Thermal management is an important parameter in an electronic packaging application. In this work, three different types of fillers such as natural graphite powder (Gr) of 50‐μm particle size, boron nitride powder (h‐BN) of 1‐μm size, and silver flakes (Ag) of 10‐μm particle size were used for thermal conductivity enhancement of neat epoxy resin. The thermal properties, rheology, and lap shear strength of the neat epoxy and its composite were investigated. The analysis showed that the loading of different wt% of Gr‐based fillers can effectively increase the thermal conductivity of the epoxy resin. It has also been observed that the thermal conductivity of the hybrid filler (Gr/h‐BN/Ag) reinforced epoxy adhesive composite increased six times greater than that of neat epoxy resin composite. Further, the viscosity of hybrid filler reinforced epoxy resin was found to be increased as compared with its virgin counterpart. The adhesive composite with optimized filler content was then subsequently subjected to determine single lap shear strength. The degree of filler dispersion and alignment in the matrix were determined by scanning electron microscopy (SEM) analysis. 相似文献
The one-pot catalytic conversion of cellulose into ethylene glycol (EG) is an attractive way of biomass utilization. However, low-cost, efficient, and stable catalysts are the premise and research challenges of industrial application. Herein, the magnetic recyclable W–Ni@C catalyst was synthesized by in-situ pyrolysis of Ni-MOFs impregnated with ammonium metatungstate. Compared with the Ni-W bimetallic catalysts prepared by the impregnation method and the sol–gel method, the W–Ni@C catalyst for cellulose hydrogenolysis reaction can achieve a higher ethylene glycol yield (67.1% vs 43.3% and 42.6%) and 100% of cellulose conversion rate. The uniformly dispersed Ni nanoparticles and abundant defective WOx were formed in a reductive atmosphere generated in pyrolysis of Ni-MOFs, which was indispensable for the hydrogenolysis of cellulose into EG. Besides, the hierarchical porous carbon derived from organic ligands in Ni-MOFs reduces the mass transfer resistance while confining Ni nanoparticles and WOx to prevent their leaching, effectively enhancing the stability of the W–Ni@C catalyst. Therefore, the remarkable catalytic performance, the simple and effective recovery method as well as satisfying stability would make W–Ni@C become a promising catalyst for the conversion of cellulose to EG.
Recently, several types of nanoparticles are frequently incorporated in reinforced epoxy resin composites. A homogeneous dispersion of these nanoparticles is still a problem. Thermoplastic nanofibrous structures can tackle this dispersion issue. Therefore, this paper investigated the effect of electrospun polyamide 6 nanofibrous structures on the mechanical properties of a glass fibre/epoxy composite. The nanofibres were incorporated in the glass fibre/epoxy composite as stand-alone interlayered structures and directly spun on the glass fibre reinforcement. Both ways of nanofibre incorporation have no negative effect on the impregnation of the epoxy. Moreover, the nanofibres remain well dispersed within the matrix. Incorporation of nanofibres increases the stress at failure in the 0°-direction, the best results are obtained when the nanofibres are directly electrospun onto the glass fibres. Optical microscopic images also demonstrate that nanofibres prevent delamination when a 90° crack reaches a neighbouring 0° ply. Furthermore, mode I tests showed a small improvement when a thin nanofibrous structure is deposited directly onto the glass fibres. When the composites are loaded under 45°, it is proven that, for an identical stress, the glass fibre composite with deposited nanofibres has less cracks than when interlayered nanofibrous structures are incorporated. Generally, it can be concluded that the addition of polyamide 6 nanofibres improves some mechanical characteristics of a glass fibre/epoxy composite. 相似文献
Uniform phenolic resin microspheres were prepared by the polycondensation of 3-aminophenol and formaldehyde. On the surface of the 3-aminophenol resin microspheres, silver nanoparticles were synthesized in situ and immobilized by simple heating. The composite was employed as a substrate for surface-enhanced Raman scattering (SERS). The SERS enhancement factor was evaluated using 4-mercaptobenzoic acid and Nile blue A as signal molecules. A highly sensitive SERS immunoassay that combined labeled antibody conjugated silver nanoparticle modified 3-aminophenol resin microspheres and coating antibody conjugated magnetic nanoparticles was fabricated to determine carcinoembryonic antigen. A linear relationship was obtained between the Raman intensity and the concentration of carcinoembryonic antigen. The limit of detection was 1.2 picograms per milliliter at a signal-to-noise ratio of three. This is believed to be the first report of a SERS immunoassay using silver nanoparticle modified 3-aminophenol resin microspheres as substrates. 相似文献
This study reveals the influence of silica nanoparticles on the cure reactions of a diglycidyl ether of bisphenol A epoxy resin. As soon as the silica nanoparticles are added to the neat resin (1, 3, and 5 vol.‐%), the total degree of conversion increases with an increasing amount of nanoparticles, and the cure reaction shows a more complex autocatalytic behaviour, which can not be described by a traditional kinetic model. Results from subsequent thermo‐mechanical analyses confirm an alteration in the microstructure attributable only to the presence of the nanoparticles in the curing stage. An amino‐rich interphase around the reactive treated particles is formed, which shifts the resin/hardener ratio, and benefits the homopolymerization of the epoxy and leads to a more highly crosslinked epoxy network. At the same time, the nanophase consists of a core‐shell structure with the rigid particle inside and a rubber‐like shell because of the excess hardener in this region.