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951.
High microwave absorption performances for single-walled carbon nanotube–epoxy composites with ultra-low loadings 总被引:1,自引:0,他引:1 下载免费PDF全文
Microwave-absorbing polymeric composites based on single-walled carbon nanotubes(SWNTs) are fabricated via a simple yet versatile method, and these SWNT–epoxy composites exhibit very impressive microwave absorption performances in a range of 2 GHz–18 GHz. For instance, a maximum absorbing value as high as 28 dB can be achieved for each of these SWNT–epoxy composites(1.3-mm thickness) with only 1 wt% loading of SWNTs, and about 4.8 GHz bandwidth,corresponding to a microwave absorption performance higher than 10 dB, is obtained. Furthermore, such low and appropriate loadings of SWNTs also enhance the mechanical strength of the composite. It is suggested that these remarkable results are mainly attributable to the excellent intrinsic properties of SWNTs and their homogeneous dispersion state in the polymer matrix. 相似文献
952.
Lei‐Lei Zhang He‐Jun Li Jin‐Hua Lu Yu‐Lei Zhang Sheng Cao Xue‐Ni Zhao Zi‐Bo He 《Surface and interface analysis : SIA》2013,45(6):973-977
In order to improve the cell compatibility of biomedical carbon/carbon composites, Ti6Al4V coatings were applied on carbon/carbon composites by magnetron sputtering technique. The microstructure and cell responses of the coatings were evaluated, and the bonding strength between the coatings and carbon/carbon composites was analyzed. The Ti6Al4V coatings modulated the surface morphology, decreased the surface roughness, improved the surface wettability and achieved a strong bonding strength to carbon/carbon composites. The cells showed larger cell extension and higher cell proliferation for the Ti6Al4V coatings than for the carbon/carbon composites. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
953.
Jiyong Hu Zhenxin Zhao Dandan Zhao Shufang Chen Jin'an Zhao Haipeng Zhao 《无机化学与普通化学杂志》2013,639(5):821-825
To investigate the effect of organic anions on coordination frameworks, the complexes [Cd(2, 6‐pydc)(bibix)2(H2O)2]n ( 1 ) and {[Cd4(2, 5‐pydc)4(bibix)4(H2O)4](H2O)8}n ( 2 ) were isolated by the reactions of 1‐{4‐[(1H‐benzoimidazol‐1‐yl)methyl]benzyl}‐1H‐benzoimidazole (bibix) and two distinct pyridyl‐dicarboxylates as organic anions with d10 metal salts. In the resulting structures, bibix adopts different coordination modes affected by the aromatic anions, which have distinct geometric structure and bonding modes. Thus, complex 1 has a 1D chain structure, whereas complex 2 has a 2D architecture. Both complexes 1 and 2 have a strong fluorescence emission, which may be tentatively assigned to metal‐perturbed intraligand interactions. 相似文献
954.
Michael A. Gunning Luke M. Geever John A. Killion John G. Lyons Clement L. Higginbotham 《Polymer Testing》2013,32(8):1603-1611
The work outlined in this paper describes the evaluation of polyhydroxybutyrate (PHB) based natural fibre composites via an extrusion – injection moulding process. Virgin PHB was compounded with two different naturally occuring plant fibres, hemp and jute, and a third, regenerated cellulose fibre, lyocell. Composite materials containing 10–30 wt% of each type of fibre were obtained by twin screw extrusion and the resultant material was injection moulded to produce tensile samples suitable for mechanical characterisation. Mechanical properties were determined using tensile, impact and flexural testing. Melt flow index and water absorption studies were also carried out on the biocomposite materials, and Fourier transform infrared spectroscopy was used to examine the bonding between the polymer and each fibre type. The rate of biodegradation was also observed by placing composite samples in compost and measuring weight loss weekly. The biocomposites produced using this method were shown to have increased rates of biodegradation whilst exhibiting significantly improved flexural properties. 相似文献
955.
Bert De Schoenmaker Sam Van der Heijden Ives De Baere Wim Van Paepegem Karen De Clerck 《Polymer Testing》2013,32(8):1495-1501
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
956.
The electro-optic and complex dielectric behaviour of an antiferroelectric liquid crystal 4-(1-methylheptyloxycarbonyl)phenyl 4′-(n-butanoyloxyprop-1-oxy)biphenyl-4-carboxylate, having chiral SmCA* and hexatic smectic phases, have been investigated. Complex dielectric permittivities were measured as a function of frequency, d.c. bias field and temperature. Spontaneous polarization was measured by the current reversal technique; tilt angle was measured under a polarizing microscope using a low frequency electric field. The electro-optic properties and dielectric behaviour of the material are compared with results obtained by DSC and polarizing optical microscopy. Dielectric relaxation processes in SmCA* and hexatic smectic phases were determined. The dielectric strength at the SmCA* to hexatic smectic phase transition is discussed in terms of coupling between the long range bond orientational order and smectic C director. It seems from the results of spontaneous polarization and dielectric relaxation spectroscopy that the material might possess an additional phase between the SmCA* and hexatic smectic I* phases. 相似文献
957.
Octa(aminophenyl)silsesquioxane (OAPS) was used as the curing agent of diglycidyl ether of bisphenol-A (DGEBA) epoxy resin. A study on comparison of DGEBA/OAPS with DGEBA/4,4′-diaminodiphenyl sulfone (DDS) epoxy resins was achieved. Differential scanning calorimetry was used to investigate the curing reaction and its kinetics, and the glass transition of DGEBA/OAPS. Thermogravimetric analysis was used to investigate thermal decomposition of the two kinds of epoxy resins. The reactions between amino groups and epoxy groups were investigated using Fourier transform infrared spectroscopy. Scanning electron microscopy was used to observe morphology of the two epoxy resins. The results indicated that OAPS had very good compatibility with DGEBA in molecular level, and could form a transparent DGEBA/OAPS resin. The curing reaction of the DGEBA/OAPS prepolymer could occur under low temperatures compared with DGEBA/DDS. The DGEBA/OAPS resin didn’t exhibit glass transition, but the DGEBA/DDS did, which meant that the large cage structure of OAPS limited the motion of chains between the cross-linking points. Measurements of the contact angle indicated that the DGEBA/OAPS showed larger angles with water than the DGEBA/DDS resin. Thermogravimetric analysis indicated that the incorporation of OAPS into epoxy system resulted in low mass loss rate and high char yield, but its initial decomposition temperature seemed to be lowered. 相似文献
958.
In the present work, structure changes during stretching of isotactic polypropylene (emPP) and emPP/silicon dioxide (SiO2) composites have been investigated systematically. The α-form crystal structure of both iPP and emPP/SiO2 composites is destroyed and transforms into the mesophase as the samples are stretched at a low temperature (35℃), while stretching at high temperatures (90℃ and 120℃) can restrain the appearance of defects and keep the perfection of crystal structure. FTIR results reveal that the stretching temperatures show no obvious difference of the effect on the orientation of pure iPP, however, the orientation of emPP/SiO2 composites is greatly changed by the tensile temperature. In the case of micron-sized SiO2 particles (average particle diameter d>1 μm), the orientation of the composites is lower than that of pure iPP at all stretching temperatures. The above results suggest that the stretching temperature and the SiO2 particle size have great influence on the structure variation and orientation behavior of emPP/SiO2 composites. 相似文献
959.
The surfaces of poly(urea-formaldehyde) (PUF) were modified by γ -glycidoxypropyltrimethoxy silane (KH560) in order to improve the interfacial bonding between self-healing PUF microcapsules and epoxy matrix. The modification mechanism between PUF microcapsules and KH560 was studied. X-ray photoelectron spectra (XPS) analyses showed that the silane coupling agent molecular binds strongly to the surfaces of PUF microcapsules. Chemical bond (Si–O–C) and hydrogen bond were formed at interface by the reaction between Si–OH and the hydroxyl group of PUF microcapsules surface. The tensile and impact resistance tests revealed that strength and toughness of the composites was improved significantly. Furthermore, scanning electronic microscopy (SEM) photographs of the fractured surface confirmed that the silane coupling agent plays an important role in improving the interfacial performance between microcapsules and resin matrix. 相似文献
960.
Yubo Chen Hao Feng Liang Li Songmin Shang Marcus Chun-Wah Yuen 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(12):1225-1229
Conducting polymer hydrogels consisting of polypyrrole (PPy) and chitosan (CS) are prepared by static polymerization of pyrrole using methyl orange (MO) as the dopant and Fe2(SO4)3 as the oxidant in the CS aqueous solution. PPy/CS composite hydrogels not only have good electrical conductivities, but also exhibit excellent swelling/deswelling behaviors due to the participation of one-dimensional conducting PPy blocks in the hydrogel network. The effects of the amount of the oxidant and ionic strength on the physical properties of PPy/CS composite hydrogels are studied in detail. The results show that PPy/CS composite hydrogels have improved water absorbencies in saline solutions compared with the conventional polyelectrolyte hydrogel. 相似文献