Interfacial mechanical properties of carbon nanotube-deposited carbon fiber epoxy matrix hierarchical composites

Functionalized multiwalled carbon nanotubes were successfully deposited on carbon fibers using four different techniques including dip coating, hand layup, spray up and electrophoretic deposition (EPD). A uniform coating of nanotubes was achieved from EPD in comparison to other coating techniques. Later nanotube-coated fibers by EPD were introduced in epoxy resin to investigate interfacial mechanical properties of the developed hierarchical composites by vacuum bagging technique. The increases in flexural and interlaminar shear properties up to 15% and 18% were observed in composites containing nanotube-coated carbon fibers than composites with virgin carbon fibers, respectively. Microscopic observation revealed the proper impregnation of multiscale reinforcements, i.e., carbon fibers and carbon nanotubes, in resin along with the modification of fiber/matrix interface due to the presence of nanotubes at interface. Finally, the mechanisms for improved mechanical properties were identified along with the presentation of a schematic model for better understanding of the improved performance of hierarchical composite after depositing uniformly dispersed nanotubes on carbon fibers.     

Adjustable thermal conductivity in carbon nanotube nanofluids

Homogeneous and stable nanofluids have been produced by suspending well dispersible multi-walled carbon nanotubes (CNTs) into ethylene glycol base fluid. CNT nanofluids have enhanced thermal conductivity and the enhancement ratios increase with the nanotube loading and the temperature. Thermal conductivity enhancement was adjusted by ball milling and cutting the treated CNTs suspended in the nanofluids to relatively straight CNTs with an appropriate length distribution. Our findings indicate that the straightness ratio, aspect ratio, and aggregation have collective influence on the thermal conductivity of CNT nanofluids.     

Dispersibility dependence of thermal conductivity of carbon nanotube based nanofluids

A differential effective medium theory together with Brownian motion is used to predict Effective Thermal Conductivity (ETC) of CNT nanofluids. ETC was influenced significantly by Brownian motion and enhancement was higher in dilute nanofluids. A theoretical model employing an effective volume fraction with dispersibility factor agrees well with experimental data.     

Microstrain in hydroxyapatite carbon nanotube composites

Synchrotron radiation diffraction data were collected from hydroxyapatite–carbon nanotube bioceramic composites to determine the crystallite size and to measure changes in non‐uniform strain. Estimates of crystallite size and strain were determined by line‐profile fitting of discrete peaks and these were compared with a Rietveld whole‐pattern analysis. Overall the two analysis methods produced very similar numbers. In the commercial hydroxyapatite material, one reflection in particular, (0 2 3), has higher crystallite size and lower strain values in comparison with laboratory‐synthesized material. This could indicate preferential crystal growth in the [0 2 3] direction in the commercial material. From the measured strains in the pure material and the composite, there was a degree of bonding between the matrix and strengthening fibres. However, increasing the amount of carbon nanotubes in the composite has increased the strain in the material, which is undesirable for biomedical implant applications.     

Roles of interfaces between carbon fibers and epoxy matrix on interlaminar fracture toughness of composites

The effect of atmospheric-pressure plasma treatment on high strength PAN-based carbon fibers had been studied in terms of fiber surface energetics and mode I and II interlaminar fracture toughness of unidirectional carbon fibers/epoxy matrix composites. The surface characterization of plasma treated carbon fibers was investigated by X-ray photoelectron spectroscopy (XPS) and contact angles. As a result, the plasma treatment changed the surface properties of the carbon fibers, mainly through formation of oxygen functional groups like hydroxyl, carbonyl, and carboxyl groups. According to contact angle measurements, it was observed that plasma treatment led to an increase in surface free energy of the fibers, mainly due to the increase of its specific component. Fracture toughness test results employing double-cantilever beam (DCB) and end notched flexure (ENF) specimens also showed that the increase in specific components or hydrogen bonding between the –OH groups on carbon fibers and the =O ring in epoxy matrix resins played an important role in improving the degree of adhesion at interfaces, resulting in an increase in the interfacial fracture toughness of the composites studied.     

The interaction between unique hyperbranched polyaniline and carbon nanotubes,and its influence on the dielectric behavior of hyperbranched polyaniline/carbon nanotube/epoxy resin composites

Novel hybridized multi-walled carbon nanotubes (CNTs), consisting of a unique hyperbranched polyaniline (HSiPA) and CNTs, were prepared. The interaction between HSiPA and CNTs was investigated by many techniques, and results show that there are strong π–π and electrostatic interactions between HSiPA and CNTs, so HSiPA can stack firmly onto the surface of CNTs to form a coating. Based on this, a new kind of ternary composites made up of hybridized CNTs and epoxy (EP) resin was prepared, the influence of the ratio of HSiPA to CNTs on the structure and properties of the HSiPA/CNT/EP composites was intensively studied. The percolation threshold of HSiPA/CNT/EP composites is very low (1.26 wt%); besides, with a suitable ratio of HSiPA to CNTs, the HSiPA/CNT/EP composite has much higher dielectric constant and lower dielectric loss than the CNT/EP composite with the same loading of CNTs. When the ratio of HSiPA to CNTs is 0.5:1, the dielectric constant and loss at 100 Hz of the resultant HSiPA/CNT0.5/EP composite are 711 and 1.53, about 7.1 and 4.3 × 10^?3 times the corresponding value of CNT0.5/EP composite, respectively. In addition, compared with traditional CNT/EP composites, the HSiPA/CNT0.5/EP composites have different equivalent circuit models. These attractive results are attributed to unique structure of hybridized CNTs, and thus leading to greatly different structures between the CNT0.5/EP and HSiPA/CNT0.5/EP composites. This investigation reported herein suggests a new approach to prepare new CNTs and related composites with controllable dielectric properties.     

Electrochemical synthesis of polypyrrole/carbon nanotube nanoscale composites using well-aligned carbon nanotube arrays

Polypyrrole/carbon nanotube nanoscale composites were successfully fabricated by electrochemical deposition of polypyrrole over each of the carbon nanotubes in well-aligned large arrays. The thickness of the polypyrrole coating can be easily controlled by the value of the film-formation charge. For both thin (low film-formation charge) and thick (high film-formation charge) films, the polypyrrole coating on the surface of each nanotube is very uniform throughout the entire length, as observed by transmission electron microscopy. Received: 2 May 2001 / Accepted: 4 May 2001 / Published online: 20 June 2001     

Electronic properties of carbon nanotube/fabric composites

Single walled carbon nanotube (SWNT)/fabric composite materials were manufactured using two simple manufacturing processes. The first method is direct deposition of SWNTs by either a spray method or by incubation; the other is a Quasi-Langmuir–Blodgett (QLB) transfer technique. The composite retains high mechanical strength (governed by the fabric), and good electrical properties (determined by the nanotubes). We measure the DC electrical conductivity of the composite fabric to be 5.33 S/cm for the sprayed tubes, 13.8 S/cm for the incubated SWNTs, and 8 S/cm for the QLB transferred tubes; these values are limited not by the nanotube network, but by the surface roughness of the fabric itself. Measurements of the conductivity up to 1 MHz reveal a transport process that proceeds along a random network, with barriers separating the various nanotubes. The material is resistive both to changes in temperature (range of 0–80 °C) and mechanical deformations. The conductivity of the composite decreases by less than 10% when bent around a cylinder of 1 cm diameter.     

Conduction noise absorption by fiber-reinforced epoxy composites with carbon nanotubes

Nearly all electronic equipment is susceptible to malfunction as a result of electromagnetic interference. In this study, glass fiber, and carbon fiber as a type reinforcement and epoxy as a matrix material were used to fabricate composite materials. In an attempt to increase the conduction noise absorption, carbon nanotubes were grown on the surface of glass fibers and carbon fibers. A microstrip line with characteristic impedance of 50 Ω in connection with network analyzer was used to measure the conduction noise absorption. In comparing a glass fiber/epoxy composite with a GF-CNT/Ep composite, it was demonstrated that the CNTs significantly influence the noise absorption property mainly due to increase in electric conductivity. In the carbon fiber composites, however, the effectiveness of CNTs on the degree of electric conductivity is negligible, resulting in a small change in reflection and transmission of an electromagnetic wave.     

Melt mixing of polycarbonate/multi-wall carbon nanotube composites

—Composites of polycarbonate (PC) with multi-wall carbon nanotubes (MWNT) of different concentrations are prepared by diluting a PC based masterbatch containing 15 wt% MWNT using melt mixing in a DACA-Micro Compounder (4 g scale). Electrical resistivity measurements indicate that the percolation of MWNT is reached between 1 and 1.5 wt%. In addition, melt rheology was applied as another sensitive method to detect the percolation of the nanotubes. Atomic Force Microscopy and visual observations of the composite dispersions in a PC-solvent were used to characterise the state of MWNT dispersion. Differential Scanning Calorimetry and Dynamic Mechanical Analysis were applied to detect changes in the glass transition temperature of PC as a result of processing and of MWNT interactions with the PC matrix including the state of dispersion. In addition, DMA confirmed the reinforcement effect of the nanotubes. The results show that the nanotube incorporation also influences the processing behaviour. Due to the enhancement in melt viscosity by adding nanotubes and the enhanced shear forces, the molecular weight of the PC in the composites is reduced as compared to PC extruded under the same conditions. This effect leads to changes in the glass transition temperature and modulus which counteracts the effects originating from the nanotube-polymer interaction.     

Processing and properties of carbon nanofibers reinforced epoxy powder composites

Commercially available CNFs (diameter 30–300 nm) have been used to develop both bulk and coating epoxy nanocomposites by using a solvent-free epoxy matrix powder. Processing of both types of materials has been carried out by a double-step process consisting in an initial physical premix of all components followed by three consecutive extrusions. The extruded pellets were grinded into powder and sieved. Carbon nanofibers powder coatings were obtained by electrostatic painting of the extruded powder followed by a curing process based in a thermal treatment at 200 °C for 25 min. On the other hand, for obtaining bulk carbon nanofibers epoxy composites, a thermal curing process involving several steps was needed. Gloss and mechanical properties of both nanocomposite coatings and bulk nanocomposites were improved as a result of the processing process. FE-SEM fracture surface microphotographs corroborate these results. It has been assessed the key role played by the dispersion of CNFs in the matrix, and the highly important step that is the processing and curing of the nanocomposites. A processing stage consisted in three consecutive extrusions has reached to nanocomposites free of entanglements neither agglomerates. This process leads to nanocomposite coatings of enhanced properties, as it has been evidenced through gloss and mechanical properties. A dispersion limit of 1% has been determined for the studied system in which a given dispersion has been achieved, as the bending mechanical properties have been increased around 25% compared with the pristine epoxy resin. It has been also demonstrated the importance of the thickness in the nanocomposite, as it involves the curing stage. The complex curing treatment carried out in the case of bulk nanocomposites has reached to reagglomeration of CNFs.     

碳纳米管/聚二甲基硅氧烷复合薄膜的制备及力敏特性研究

针对传感器的敏感单元发展需求,提出了一种碳纳米管复合材料.该材料是以碳纳米管作为填充粒子,结合聚二甲基硅氧烷(PDMS)有机基体,采用超声共混方法制备的一种新型传感器敏感元件.详细分析研究了复合材料的制备工艺参数,以及在不同工艺参数下该复合材料的力敏特性.扫描电镜测试表明碳纳米管在PDMS中分散均匀且镶嵌良好.通过对不同体积分数的碳纳米管与PDMS复合材料进行电学性能测试,研究薄膜的"力-电阻"和"力-电容"耦合性能,测试了薄膜结构的力敏效应.计算得到复合薄膜材料的压阻灵敏度因子达到40,压电容灵敏度因子达到70.实验研究表明,通过改变碳纳米管与PDMS的比例,可以很好地调节其电子输运特性以及电阻和电容的应力敏感特性,可以为该类型的力敏材料在不同的力敏传感技术领域提供新的研究思路.     

Impedance spectroscopy of carbon nanotube/solid polymer electrolyte composites

New composite polymer electrolytes (CPE) have been prepared by a solution-casting technique, using polyethylene oxide, lithium hexafluorate (LiPF₆) as the doping salt, ethylene carbonate (EC) as the plasticizer and amorphous carbon nanotubes (αCNTs) as the filler. The crystallinity and ionic conductivity of the CPE are examined. Differential scanning calorimetry shows a decrease in melting temperature and crystallinity upon the addition of LiPF₆, EC and αCNTs to the polymer electrolyte system. The addition of salt increases the conductivity up to 10⁻⁵ S cm⁻¹. The incorporation of EC and αCNTs into the salted polymer shows a significant conductivity increase of 10⁻⁴ and 10⁻³ S cm⁻¹. The complexation process is examined using Fourier transform infrared spectroscopy. The Vogel-Tamman-Fulcher (VTF) plots suggest that the temperature dependence of conductivity is a thermally activated process.     

Nonlinear resistance of polymer composites with carbon nanotube additives in the percolation state

The electrical properties of a polymer composite with carbon nanotube additives have been analyzed. The state of the system near the percolation threshold, when charge is transferred along a single percolation path, has been considered. For this state, the current–voltage characteristics of a percolation chain made up of carbon nanotubes have been calculated under the assumption that the contact resistance between neighboring nanotubes is much higher than the intrinsic resistance of the nanotubes. According to recent data, the distance between neighboring (contacting) nanotubes has been assumed to be randomly distributed. It has been shown that, under the given conditions, the current–voltage characteristic is essentially nonlinear. This indicates the nonohmic conductivity of the composites. The dependence of the current–voltage characteristic on the spread of the contact distribution over distances has been discussed.     

碳纳米管/聚苯胺纳米复合管的制备及其微波介电特性研究

用原位乳液聚合法在碳纳米管表面包覆聚苯胺，制备出了碳纳米管/聚苯胺一维纳米复合管.复合管的直径为50—80 nm，聚苯胺包覆层的厚度为20—30 nm，聚苯胺在碳纳米管表面以层状和枝晶状两种形态生长.研究了碳纳米管/聚苯胺复合管在2—18 GHz的微波介电特性.与纯碳纳米管相比，碳纳米管/聚苯胺复合管的介电常数的实部ε′和虚部ε″在2—18 GHz随频率变化较小，在低频波段介电常数值较小，作为微波吸收剂容易实现与自由空间的阻抗匹配，而且它的介电损耗角正切(tanδ=ε″/ε′)较高，是一种很好的微波吸收剂. 关键词： 碳纳米管 聚苯胺 微波介电特性 微波吸收剂     

纳米CdS/碳纳米管复合材料的光电特性

基于CdS良好的光学性质和单壁碳纳米管(SWCNT)优异的电子学性质, 制备了纳米CdS/SWCNT复合材料和纳米CdS/聚乙烯亚胺(PEI)功能化SWCNT复合材料, 并利用日光灯光源模拟太阳光研究了它们的光电性质. 结果表明, 纳米CdS/SWCNT复合材料呈现显著的负光电导现象, 而纳米CdS/PEI-SWCNT复合材料呈现强烈的正光电导现象. 用电子转移理论对这一结果进行了解释. 两样品在大角度弯折的情况下, 光电性质均基本没有变化. 因此, 纳米CdS/碳纳米管复合材料在光电领域, 尤其是新兴的柔性光电子学领域有着良好的应用前景. 关键词： 碳纳米管 CdS 光电材料 复合材料     

Interphase characterization in epoxy resin/carbon fibre composites

In this paper, interphase properties of carbon fibre/epoxy resin single-fibre model and unidirectional (UD) composites are reported. To study the contribution of the carbon fibre surface chemistry and morphology and of the resin itself to the overall properties of the composites, untreated, oxidized and sized fibres are used with bi- and tetrafunctional, diglycidylether of Bisphenol A, DGEBA and tetraglycidyl 4,4'-diaminodiphenylmethane, TGDDM-based resins, cured with amine and anhydride hardeners. Adsorption measurements and single fibre contact angle experiments, as well as the pull-out test were applied to characterize the surface of carbon fibre and the interfacial shear strength with different matrices. It was shown that the presence of the size on the surface can drastically affect the wettability as well as the starting rate of the cure reaction of epoxide in the vicinity of the fibre surface, as revealed by FTIR microscopy. Different elastic-plastic behavior of model composites before debonding is found for untreated, oxidized and sized fibres, due to the various interphase structures formed. Both micro-and macromechanical properties of the composites are found to be significantly affected by the matrix properties. The role of the surface treatment of fibers becomes especially important in high performance resin systems.     

Rheological behaviour of ethylene glycol-titanate nanotube nanofluids

Experimental work has been performed on the rheological behaviour of ethylene glycol based nanofluids containing titanate nanotubes over 20–60 °C and a particle mass concentration of 0–8%. It is found that the nanofluids show shear-thinning behaviour particularly at particle concentrations in excess of ~2%. Temperature imposes a very strong effect on the rheological behaviour of the nanofluids with higher temperatures giving stronger shear thinning. For a given particle concentration, there exists a certain shear rate below which the viscosity increases with increasing temperature, whereas the reverse occurs above such a shear rate. The normalised high-shear viscosity with respect to the base liquid viscosity, however, is independent of temperature. Further analyses suggest that the temperature effects are due to the shear-dependence of the relative contributions to the viscosity of the Brownian diffusion and convection. The analyses also suggest that a combination of particle aggregation and particle shape effects is the mechanism for the observed high-shear rheological behaviour, which is also supported by the thermal conductivity measurements and analyses.     

Rapid microwave-assisted synthesis and electrochemical characterization of gold/carbon nanotube composites

Hybrid nanostructures composed of gold nanoparticles (NPs) and carbon nanotubes (CNTs) have been prepared by a microwave-assisted method in the mixed solvents of oleylamine and oleic. The morphology, structure and composition of as-obtained Au/CNT composites are characterized by transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD). The composites show characteristic plasmon absorption of Au NPs in the Ultraviolet–visual spectrum. Fourier transform infrared spectrum shows the successful introduction of functional groups on the surface of CNTs, which are crucial factors to assist the nucleation in situ of Au NPs on the surface of CNTs. Electrochemical measurements show the enhancement electrochemical response for the gold electrode modified with Au/CNT composites.     

Physico-chemical characterization of the fibre/matrix interaction in polyethylene fibre/epoxy matrix composites

The interphase in polyethylene fibre/epoxy matrix composites is studied with FT-IR microspectroscopy using a set-up to investigate the matrix as close to the fibre as a few μm or less. It is shown that moisture present on the fibre surface is able to influence the polymerization reaction of the epoxy/anhydride matrix in an irreversible manner. This effect is enhanced for composites from the more hydrophilic polyvinylalcohol fibre. The fibre/matrix interaction in these thermoplastic fibre composites is also studied with DSC through the characterization of the fibre melting. A decreased 'DSC interaction parameter' is found if the composition of the interphase is changed by moisture. For a composite with an epoxy/amine matrix, on the other hand, the DSC interaction parameter is unaffected by moisture from the fibre surface.