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1.
    
In this article, the interphase thickness in polymer carbon nanotubes (CNTs) nanocomposites (PCNT) is correlated to CNT radius and the extent of conductivity transportation from CNT to polymer matrix surrounding the CNT (K). In addition, CNT properties and “K” are applied to suggest the simple equations for percolation threshold and the fraction of networked CNT. A simple model is developed to predict the conductivity of PCNT assuming CNT size, “K” and tunneling resistance. The impacts of different parameters on the interphase thickness, percolation threshold, the fraction of networked CNT, and the conductivity of nanocomposites are studied and many experimental results are used to confirm the predictions. Thin and large CNT as well as high “K” cause low percolation threshold, large conductive networks and desirable conductivity in nanocomposites. Moreover, high tunneling resistivity and large tunneling distance negatively affect the conductivity, but the exceptional CNT conductivity is ineffective. The reasonable roles of all parameters in the predicted conductivity and the fine agreement between predictions and experimental results confirm the developed model.  相似文献   

2.
    
This article expresses a simple model for prediction of conductivity in polymer carbon nanotubes (CNT) nanocomposites (PCNT). This model suggests the roles of CNT concentration, CNT dimensions, CNT conductivity, the percentage of networked CNT, interphase thickness and tunneling properties in the conductivity of PCNT. The suggested model is applied to predict the conductivity in several samples. In addition, the significances of all parameters attributed to CNT, interphase and tunneling regions on the predicted conductivity are justified to confirm the suggested model. The calculations of conductivity properly agree with the experimental results demonstrating the capability of suggested model for prediction of conductivity. Thick interphase increases the conductivity of nanocomposites, because it enlarges the conductive networks. In addition, high tunneling resistivity due to polymer layer, large tunneling distance between adjacent CNT and small tunneling diameter deteriorate the conductivity, because they enhance the tunneling resistance limiting the charge transferring via tunneling regions. The suggested model can replace the available models to predict the conductivity in future researches.  相似文献   

3.
    
This article develops simple equations for tunneling distance between adjacent nanoparticles (d) and electrical conductivity of polymer/carbon nanotubes (CNT) nanocomposites (PCNT). The developed model considers the significances of CNT dimensions and waviness as well as interphase region surrounding CNT on the conductivity of nanocomposites. Moreover, d is defined by the sizes of CNT, interphase thickness and network density. The roles of all parameters for nanoparticles, interphase, percolation threshold and conductive network in the nanocomposite conductivity and tunneling distance are determined. Among the studied parameters, the fraction of percolated CNT of 0.6 and d = 1 nm provide the highest conductivity of PCNT, while d > 2.5 nm cause an insulated nanocomposite. In addition, the high concentration of thin CNT, a thick interphase, poor waviness, low percolation threshold, and the small fraction of percolated CNT produce an optimized level for d.  相似文献   

4.
    
Jang-Yin and Deng-Zheng equations for electrical conductivity of polymer carbon nanotubes (CNTs) nanocomposites (PCNT) are developed assuming the roles of networked CNTs, interphase, and tunneling regions. The developed models are coupled to formulate the operative resistance of a unit cell (Reff) induced by networked CNTs and tunneling region. The suggested equation is applied to calculate the operative resistance at dissimilar ranges of all parameters. In addition, the experimental measurements of conductivity for some samples are used to examine the predictability of the models. The models correctly predict the conductivity for various samples. Moreover, the parametric analyses demonstrate the sensible impacts of all parameters on the operative resistance justifying the suggested equation. A petite tunneling distance, wide tunnel, and poor polymer tunneling resistivity meaningfully deteriorate the operative resistance.  相似文献   

5.
    
The operative interphase properties surrounding carbon nanotubes (CNTs) networks are applied to progress a simple and applicable simulation for the strength of nanocomposites. Both critical interfacial shear strength (τc) and interfacial shear strength (τ) define the operative depth and power of interphase area. The experimental results of selected examples and the parametric analyses are employed to accept the established model. The experimental data properly fit to the model's forecasts and all parameters reasonably affect the nanocomposite's strength. Very low τc (10 MPa) and extremely high τ (400 MPa) significantly improve the strength of nanocomposites by 700%, while τc > 43 MPa slightly increase the nanocomposite's strength. The strongest and the densest interphase around CNT nets can raise the strength of nanocomposites by 450%, but very poor or thin interphase only changes the nanocomposite's strength by 10%. Additionally, the narrowest and the biggest CNT produce the sturdiest samples, while thick CNT (CNT radius > 11 nm) cannot strengthen the polymer media.  相似文献   

6.
    
In this work, we focus on the minimum interfacial shear modulus (Sc) and interfacial shear modulus (Si) controlling the efficiency of interphase zone in polymer clay nanocomposites, since the stress transferring through interphase section handles the stress bearing of samples. The roles of “Sc” and “Si” in the effective thickness and concentration of interphase zone are clarified. Moreover, a model based on Kolarik system is developed for modulus of clay-reinforced nanocomposites, which reflects the efficiency of interphase zone. The experimental data of tensile modulus for many samples display good matching with the predictions of the advanced model. Also, all model parameters properly manipulate the nanocomposite's modulus. Thick clay (t > 4 nm) cannot generate the interphase zone in the samples. A poor “Sc,” high “Si,” and thin clay improve the modulus of nanocomposites, but very high “Sc,” extremely poor “Si,” or thick clay cause a poor nanocomposite. A high value of Sc = 0.21 GPa deteriorates the reinforcing efficiency of clay in nanocomposites. Furthermore, low Si < 35 GPa produces a poorer nanocomposite than the polymer matrix. Additionally, complete exfoliation of thin clay (t = 1 nm) causes 900% improvement in the nanocomposite's modulus.  相似文献   

7.
8.
In this work, we investigate the compatibilizing mechanism of nanoclay in binary polymer blends by measuring the interfacial tension of polystyrene/polyamide 6, PS/PA6, as a typical system, in the presence of nanoclay. The interfacial tension of PA6 nanocomposites and PS are determined with the breaking thread method by employing the Tomotika theory. The interfacial tension is reduced when organoclay is incorporated in the PA6 phase. To investigate the effect of the localization of nanoclay, nanoclay is intentionally located at the interface of PA6 and PS. Microscopic observations show that PA6 fiber remain unchanged and does not go through break-up process; therefore, one can deduce that the apparent interfacial tension of the system reduces significantly when nanoclay particles saturate the interface.  相似文献   

9.
The viscosity of immiscible polymer blends has been studied via application of certain aspects of rheology. A symmetric mixture rule was derived, and the deviations from the ‘additivity rule’ have been associated, essentially, with the properties of the interphase, with its influence on the effective volumes of the two polymers constituting the blend and with the deformability of both the interphase and the disperse phase. The rule predicts a positive deviation for a mixture with a disperse-phase viscosity (ηd) greater than that (ηm) of the continuous medium, and a much higher-viscosity interphase, i.e. ηi å ηd ≥ ηm. Negative deviation is to be expected when the interphase has a much lower viscosity than those of the two pure polymers (ηd, ηm å ηi) in the blend. The viscosity and strength of the interphase depend mostly on the specific thermodynamic interactions that led to its creation.  相似文献   

10.
    
This paper presents a comprehensive molecular dynamics study on the effects of the stoichiometric ratio of epoxy:hardener, hardener's linear and cyclic structure, and number of aromatic rings on the interfacial characteristics of graphene/epoxy nanocomposite. The van der Waals gap and polymer peak density as a function of the type of the hardener is calculated by analyzing the local mass density profile. Additionally, steered molecular dynamics are used to conduct normal pull-out of graphene to study the effect of the mentioned features of hardeners on the interfacial mechanical properties of nanocomposites, including traction force, separation distance, and distribution quality of reacted epoxide rings in the epoxy. Influence of the hardeners on the damage mechanism and its initiation point are also studied by analyzing the evolution of local mass density profile during the normal pull-out simulation. It is seen that stoichiometric ratio and geometrical structure of the hardeners affect the interfacial strength. It is also revealed that the hardener type can change the epoxy damage initiation point. The damage occurs in the interphase region for a higher stoichiometric ratio or cyclic structure of hardener. In comparison, for hardener's lower stoichiometric ratio and non-cyclic structure, failure begins in the epoxy near graphene layers.  相似文献   

11.
    
Phase change materials (PCMs) function based on latent heat stored on or released from a substance over a slim temperature range. Multiwalled carbon nanotubes (MWCNTs) and polyaniline are important elements in sensor devices. In this work, pristine and polyaniline‐grafted MWCNTs (PANI‐g‐MWCNTs) were applied as conductive carbon‐based fillers to make PCMs based on paraffin. The attachment of PANI to the surface of MWCNTs was proved by Fourier transform Infrared analysis. Dispersion of MWCNTs in paraffin was studied by wide‐angle X‐ray scattering. Heating and solidification of PCM nanocomposites were investigated by differential scanning calorimetry, while variation in nanostructure of PCMs during heating/solidification process was evaluated by rheological measurements. It was found that after 30 min of sonication, the samples filled with 1 wt % MWCNTs have melting and solidification temperatures of 29 and 42 °C, respectively. It was also found that PANI attachment to MWCNTs significantly changes thermal conductivity behavior of PCM nanocomposites. The developed MWCNTs‐based sensor elements responded sharply at low MWCNTs content, and experienced an almost steady trend in conductivity at higher contents, while PANI‐g‐MWCNTs sensor followed an inverse trend. This contradictory behavior brought insight for understanding the response of PCMs against thermal fluctuations. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45389.  相似文献   

12.
    
In this work, the shape effect of silver nanoparticles (AgNPs) on photocatalysis and electrical conductivity was investigated. Different shapes of AgNPs achieved using various concentrations of NaBH4 were characterized using particle size analysis, UV–visible spectroscopy and high‐resolution transmission electron microscopy. The colours of colloidal solutions were found to be influenced by the shape of the nanoparticles. Yellow and blue AgNPs were spherical and triangular in shape, respectively, whereas distorted spherical particles showed a red colour and the presence of both particles in one solution resulted in a green colloidal solution. The AgNPs were used to prepare Ag/poly(vinyl alcohol) (PVA) composite films and their electrical conductivity was investigated. Owing to their better charge carrier generation, uniform distribution in the PVA matrix and enhanced surface plasmon resonance, blue AgNPs (triangular shaped) exhibited superior conductivity performance compared to the other nanoparticles. The values for maximum conductivity for the blue and yellow AgNPs were 3.45 × 10?4 Ω?1 cm?1 and 2.67 × 10?4 Ω?1 cm?1respectively. © 2019 Society of Chemical Industry  相似文献   

13.
Hybrid solid polymer electrolytes (HSPE) of high ionic conductivity were prepared using polyethylene oxide (PEO), polyacrylonitrile (PAN), propylene carbonate (PrC), ethylene carbonate (EC), and LiClO4. These electrolyte films were dry, free standing, and dimensionally stable. The HSPE films were characterized by constructing symmetrical cells containing nonblocking lithium electrodes as well as blocking stainless steel electrodes. Studies were made on ionic conductivity, electrochemical reaction, interfacial stability, and morphology of the films using alternating current impedance spectroscopy, infrared spectroscopy, and scanning electron microscopy. The properties of HSPE were compared with the films prepared using (i) PEO, PrC, and LiClO4; and (ii) PAN, PrC, EC, and LiClO4. The specific conductivity of the HSPE films was marginally less. Nevertheless, the dimensional stability was much superior. The interfacial stability of lithium was similar in the three electrolyte films. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 65: 2191–2199, 1997  相似文献   

14.
Polycarbazole (PCB) was synthesized via an interfacial polymerization method using carbazole monomer and ammonium persulfate as the oxidizing agent. The effects of surfactant type (non‐ionic Tween 20, cationic cetyltrimethylammonium bromide (CTAB) and anionic sodium dodecylsulfate) and concentration on the synthesized PCB were investigated based on the roles of micelle formation. Electron microscopy images revealed various PCB morphologies depending on the surfactant type and concentration. The newly found morphological structures of the PCB were macroporous honeycomb, connected hollow sphere and smaller hollow sphere depending on the surfactant type. The highest electrical conductivity of doped PCB_CTAB obtained was 11.3 ± 0.36 S cm?1. The electrical conductivity values of the doped PCB synthesized with CTAB were higher than that without a surfactant by three orders of magnitude. © 2016 Society of Chemical Industry  相似文献   

15.
In this work, polymer nanocomposites consisting of a poly(vinyl chloride) (PVC) and polyvinylidene fluoride (PVDF) polymer network with ZnO nanoparticles as a dopant were prepared by solution casting. An XRD study of the PVC/PVDF/ZnO polymer nanocomposites shows predominantly sharp and high intensity peaks. However, the intensity and sharpness of the XRD peaks decreases with further increment in loading of ZnO (wt%), which reveals a proper intercalation of ZnO nanoparticles within the PVC/PVDF polymer system. Fourier transform infrared spectroscopy has been used to verify the chemical compositional change as a function of ZnO nanoparticle loading. TGA analysis clearly describes the thermal degradation of the pure polymer and polymer nanocomposites. The complex dielectric function, AC electrical conductivity and impedance spectra of these nanocomposites were investigated over the frequency range from 10 Hz to 35 MHz. These spectra were studied with respect to the Wagner ? Maxwell ? Sillars phenomenon in the low frequency region. Nyquist plots of the PVC/PVDF/ZnO nanocomposites were established from impedance measurements. The temperature‐dependent DC ionic conductivity obtained from the Nyquist plots follows Arrhenius behaviour. © 2016 Society of Chemical Industry  相似文献   

16.
A two‐step method is suggested to predict the Young's modulus of polymer nanocomposites assuming the interphase between polymer matrix and nanoparticles. At first, nanoparticles and their surrounding interphase are assumed as effective particles with core–shell structure and their modulus is predicted. At the next step, the effective particles are taken into account as a dispersed phase in polymer matrix and the modulus of composites is calculated. The predictions of the two‐step method are compared with the experimental data in absence and presence of interphase and also, the influences of nanoparticles size as well as interphase thickness and modulus on the Young's modulus of nanocomposites are explored. The predictions of the suggested model show good agreement with the experimental data by proper ranges of interphase properties. Moreover, the interphase thickness and modulus straightly affect the modulus of nanocomposites. Also, smaller nanoparticles create a higher level of modulus for nanocomposites, due to the large surface area at interface and the strong interfacial interaction between polymer matrix and nanoparticles.

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17.
    
Flexible conductive composites based on an elastomer, ethylene–vinyl acetate copolymer (EVM), and multiwalled carbon nanotubes (MWCNTs) were fabricated by melt‐blending and subsequent crosslinking. Two types of ionic liquids (ILs), tributylmethylammonium bis(trifluoromethanesulfonyl)imide and 1‐ethyl‐3‐methylimidazolium tetrafluoroborate, were used to modify the MWCNTs for the purpose of improving their dispersion in the polymer matrix. It was found that the MWCNTs modified by an individual IL form agglomerates in the EVM matrix, while the MWCNTs modified by the two types of ILs simultaneously disperse in the EVM matrix homogeneously. Moreover, nanocomposites based on the MWCNTs modified with the combination of the two ILs exhibit improved mechanical and electrical properties. The mechanism of such synergistic effects was investigated. It was found that EVM is miscible with tributylmethylammonium bis(trifluoromethanesulfonyl)imide and it is immiscible with 1‐ethyl‐3‐methylimidazolium tetrafluoroborate. On the other hand, MWCNTs show stronger interaction with 1‐ethyl‐3‐methylimidazolium tetrafluoroborate than tributylmethylammonium bis(trifluoromethanesulfonyl)imide. Therefore, the uniform dispersion of MWCNTs in the EVM matrix is attributed to ‘bridging’ effects of the two ILs due to the different interactions of the two ILs with MWCNTs and EVM. The application of MWCNTs modified with two types of ILs in a polymer matrix opens a new fabrication strategy for high‐performance polymer nanocomposites. © 2017 Society of Chemical Industry  相似文献   

18.
The synthesis, diffraction patterns, thermal stability, and ionic conductivity properties of methacrylate‐type polymers are analyzed here to assess their feasibility as polymer electrolytes. From the parent polymer, poly (N,N‐dimethylaminoethylmethacrylate), herein labeled PDMAEMA, a protonated derivative was used to prepare polymer/Montmorillonite nanocomposites with various clay contents (1, 3, and 5 wt %). AC spectroscopy provided the ionic conductivity data for the polymers and clay–polymer nanocomposites. Evidences of nanocomposite formation are shown using transmission electron microscopy and wide‐angle X‐ray diffraction. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   

19.
20.
介绍了通过机械混炼法制备碳纳米管束(CNTB)一元增强,碳纳米管束/白炭黑二元增强,碳纳米管束/炭黑/白炭黑三元增强以复合材料的方法。其中的二元与三元增强复合材料,又研究了Si747的添加与否对复合材料的性能影响。我们进行此研究的目的在于探索在一元,二元,三元以及由Si747添加的几种体系中,碳纳米管束的添加量对复合材料体积电阻率的影响。通过TEM研究了不同复合材料中填料的分散情况,通过导电性能测试,研究了在三种增强体系中,碳纳米管的导电网络效应。经研究我们发现: (1)在碳纳米管束/白炭黑二元增强体系中,当CNTB的填充体积分数一致时,当白炭黑的填充分数从0phr,20phr增加到50phr时,复合材料的导电性能是逐渐变差的。但当白炭黑的填充量到达70phr时,复合材料的导电性发生了突变,其导电性能突然变好,其体积电阻率甚至要好于填充0phr白炭黑的碳纳米管束一元增强的复合材料; (2)在碳纳米管束/炭黑/白炭黑三元增强体系中,我们尝试了用等量炭黑替代白炭黑,当保证CNTB的填充体积一致时,我们发现随着等量替代的白炭黑的炭黑的质量增加,复合材料的导电性能逐渐变好: (3)在碳纳米管束/白炭黑二元增强体系和碳纳米管束/炭黑/白炭黑三元增强体系中,在保证各个填料的质量不变的情况下,我们尝试了用Si747对复合材料进行了改性,结果发现,经过Si747改性的复合材料的体积电阻率要明显好于未经过Si747改性的复合材料。  相似文献   

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