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1.
Polyethylene multiwalled carbon nanotube composites   总被引:4,自引:0,他引:4  
Polyethylene (PE) multiwalled carbon nanotubes (MWCNTs) with weight fractions ranging from 0.1 to 10 wt% were prepared by melt blending using a mini-twin screw extruder. The morphology and degree of dispersion of the MWCNTs in the PE matrix at different length scales was investigated using scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM) and wide-angle X-ray diffraction (WAXD). Both individual and agglomerations of MWCNTs were evident. An up-shift of 17 cm−1 for the G band and the evolution of a shoulder to this peak were obtained in the Raman spectra of the nanocomposites, probably due to compressive forces exerted on the MWCNTs by PE chains and indicating intercalation of PE into the MWCNT bundles. The electrical conductivity and linear viscoelastic behaviour of these nanocomposites were investigated. A percolation threshold of about 7.5 wt% was obtained and the electrical conductivity of PE was increased significantly, by 16 orders of magnitude, from 10−20 to 10−4 S/cm. The storage modulus (G′) versus frequency curves approached a plateau above the percolation threshold with the formation of an interconnected nanotube structure, indicative of ‘pseudo-solid-like’ behaviour. The ultimate tensile strength and elongation at break of the nanocomposites decreased with addition of MWCNTs. The diminution of mechanical properties of the nanocomposites, though concomitant with a significant increase in electrical conductivity, implies the mechanism for mechanical reinforcement for PE/MWCNT composites is filler-matrix interfacial interactions and not filler percolation. The temperature of crystallisation (Tc) and fraction of PE that was crystalline (Fc) were modified by incorporating MWCNTs. The thermal decomposition temperature of PE was enhanced by 20 K on addition of 10 wt% MWCNT.  相似文献   

2.
In order to ensure better rubber/multi-walled carbon nanotube (MWCNT) compatibility and to enhance the dispersibility, a series of ionic liquids has been tested in regard to an improved interaction between rubber and carbon nanotubes. We found that in the presence of especially one ionic liquid, namely, 1-allyl-3-methyl imidazolium chloride, for the blend of solution-styrene-butadiene and polybutadiene rubber, used as basic elastomer, a three fold increase of tensile strength was achieved with only ∼3 wt.% MWCNT loading. At this low concentration of MWCNTs the sample can be stretched up to 456% without mechanical failure. The use of this ionic liquid additionally results in higher electrical conductivity (10−2 S cm−1) at low concentration (<3 wt.%) of MWCNTs. Dynamic mechanical analysis confirmed the specific interaction of CNTs and diene rubber chains by showing an extra relaxation process at relatively higher temperature (∼Tg + 130 K) in the temperature sweep measurements. Raman spectroscopic analysis also supported the specific interaction between MWCNTs and rubber molecules with the help of 1-allyl-3-methyl imidazolium chloride. Transmission electron microscopic images confirm the good dispersion of the MWCNTs along with a ‘cellular’-like structure of the CNTs in the rubber matrix.  相似文献   

3.
A method is reported that involves the bulk polymerization of styrene monomer in the presence of multi-wall carbon nanotubes (MWCNTs) and polystyrene (PS) beads, for the preparation of MWCNT/PS conducting composites with a significantly lower (0.08 wt.% MWCNT) percolation threshold than previously reported. Thus, the conductivities of 7.62 × 10−5 and 1.48 × 10−3 S cm−1 were achieved in the MWCNT/PS composites through homogeneous dispersion of 0.08 and 0.26 wt.% CNTs, respectively in the in situ polymerized PS region by using 70 wt.% PS beads during the polymerization. The extent of dispersion and location of the MWCNTs in the PS matrix has been investigated with a scanning and transmission electron microscopy. The conductivity of the composites was increased with increasing wt.% of the PS beads at a constant CNT loading, indicating the formation of a more continuous network structure of the CNTs in PS matrix.  相似文献   

4.
Cheng Yang 《Carbon》2009,47(4):1096-2058
Flexible dielectric polystyrene based composites containing multi-walled carbon nanotubes (MWCNTs) were reported. The MWCNTs were coated with polypyrrole (PPy) by an inverse microemulsion polymerization. Transmission electron microscopy, X-ray photoelectron spectroscopy and Raman spectroscopy indicated that the MWCNTs were coated with PPy. Our composites presented a stable high dielectric constant (∼44), rather low loss (<0.07), and large energy density (up to 4.95 J cm−3). The largely-enhanced dielectric performance originates from the organic shell PPy, which not only ensure good dispersion of MWCNTs in the polymer matrix but also screen charge movement to shut off leakage current. Such MWCNT composites can be used to store charge and electrical energy and play a key role in modern electronics and electric power systems.  相似文献   

5.
Multiwalled carbon nanotubes (MWCNTs) were dispersed and distributed via a co-rotating twin-screw extruder (TSE) in high (h)- and low (l)-molecular-weight amorphous and semicrystalline polylactides (PLAs) (aPLA and scPLA, respectively). Effects of PLA molecular weight and D-lactic acid equivalents content (D-content), as well as processing parameters, were examined on the MWCNT dispersion quality in PLA. The effectiveness of the MWCNT dispersion in various PLA matrices was investigated using scanning electron microscopy (SEM) and small-amplitude oscillatory and transient shear flow rheometry in the molten state. The results showed a better dispersion of MWCNTs in the low-molecular-weight PLA grades (aPLAl and scPLAl). In addition, better MWCNT dispersion was observed in aPLA grades when processed at a higher temperature of 190°C than at 150°C. At 150°C, while MWCNT bundles in aPLAl could be broken down, a good dispersion could not be achieved in aPLAh due to the lower molecular mobility at such a temperature. The electrical conductivity of the samples was also shown to increase as the MWCNT dispersion was improved. The existence of crystallites in scPLA-based nanocomposites, however, disrupted the connectivity of the MWCNTs and decreased the final electrical conductivity. The lower molecular weight aPLAl prepared at 190°C showed the highest electrical conductivity (~10−5 S/m) at a low loading of 0.5 wt.% MWCNTs.  相似文献   

6.
Two representative polybenzazoles, poly(p-phenylene benzobisoxazole) (PBO) and poly(2,5-benzoxazole) (ABPBO), have been used as matrix materials for fabricating electrically conducting nanocomposite films. In this strategy, pristine multi-walled carbon nanotubes (MWCNTs) were first treated with nitric acid to form carboxylated multi-walled carbon nanotubes (MWCNTs-COOH). Subsequently, MWCNTs-COOH were dispersed efficiently in the methanesulfonic acid (MSA) solution of polybenzazole, sonicated, and then processed into thin films. MWCNTs-COOH in MSA formed an isotropic regime at the concentration of ∼0.1 wt.%. Nanotubes could form net like structures and conductive channels in the polymer matrix to improve electrical conductivity, mechanical properties, and thermal stability. At the MWCNT-COOH composition of 5 wt.%, polybenzazole/MWCNT-COOH composite films exhibited a dramatic enhancement in electrical conductivity by 8 orders of magnitude from ∼10−12 to 1.6 × 10−4 S cm−1 without significantly sacrificing optical transparency.  相似文献   

7.
Covalent functionalization of multi-wall carbon nanotubes (MWCNTs) with minimal alteration to the MWCNT surface is important to achieve homogenously dispersed carbon nanotubes while maintaining their unique mechanical and electrical properties. Carboxylic acid derivatized MWCNTs (MWCNT-COOH) were covalently functionalized with 3,3′-iminobis(N,N-dimethylpropylamine) (DMPA). Upon subsequent quaternization of DMPA, dendritic ammonium cation-functionalized MWCNTs (MWCNT-DMPA+) were formed, where two ammonium cations were incorporated per amide site. Thermogravimetric analysis and X-ray photoelectron spectroscopy demonstrated successful covalent functionalization and formation of the surface-bound ammonium salt. Raman spectroscopy and atomic force microscopy indicated the absence of an appreciable decrease in the MWCNT aspect ratio. Compared with pristine MWCNTs and MWCNT-COOH, MWCNT-DMPA+ exhibited enhanced dispersibility in N,N-dimethylformamide (DMF) as observed with UV–Visible spectroscopy and transmission electron microscopy (TEM). In addition, blending the cation-bound MWCNT-DMPA+ with anion-bound sulfonated polyurethane in DMF generated novel composites with a nanotube content ranging from 0.5 to 5 wt.%. Characterization of the composite films using both field emission scanning electron microscopy and TEM revealed that MWCNT-DMPA+ exhibited uniform dispersion in sulfonated polyurethane matrices even at 5 wt.%. Tensile analysis showed that the modulus of the sulfonated polyurethane matrix linearly increased with MWCNT-DMPA+ content.  相似文献   

8.
Multi-walled carbon nanotube (MWCNT)/polyimide composite films were fabricated through electrophoretic deposition (EPD) of MWCNT-polyamic acid colloidal suspension which was derived from carboxylated-MWCNTs and poly(pyromellitic dianhydride-co-4,4′-oxydianiline) (PMDA-ODA). Under electric field, both negatively charged MWCNTs and PMDA-ODA colloid particles migrate onto a positively charged anode simultaneously, and are converted to a coherent MWCNT/polyimide composite film in the ensuing imidization reaction. Uniform dispersion of MWCNTs in the composite film was observed using transmission electron microscopy. The thickness of the prepared composite film can be tuned by varying processing conditions such as deposition time and anode conductivity. The electrical conductivity of the composite film increased with increasing the concentration of MWCNTs in EPD suspension. The mechanical reinforcement of polyimide using MWCNTs was evaluated by tensile testing and nanoindentation testing.  相似文献   

9.
Here, we demonstrate an easy method for the preparation of highly electrically conductive polycarbonate (PC)/multiwalled carbon nanotubes (MWCNTs) nanocomposites in the presence of poly(butylene terephthalate) (PBT). In the presence of MWCNTs, PC and PBT formed a miscible blend, and the MWCNTs in the PC matrix were uniformly and homogeneously dispersed after the melt mixing of the PC and PBT–MWCNT mixture. Finally, when the proportion of the PC and PBT–MWCNT mixture in the blend/MWCNT nanocomposites was changed, an electrical conductivity of 6.87 × 10?7 S/cm was obtained in the PC/PBT–MWCNT nanocomposites at an MWCNT loading as low as about 0.35 wt %. Transmission electron microscopy revealed a regular and homogeneous dispersion and distribution of the MWCNTs and formed a continuous conductive network pathway of MWCNTs throughout the matrix phase. The storage modulus and thermal stability of the PC were also enhanced by the presence of a small amount of MWCNTs in the nanocomposites. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013  相似文献   

10.
In this work, a novel nano-sulfur/MWCNTs composite with modified multi-wall carbon nano-tubes (MWCNTs) as sulfur-fixed matrix for Li/S battery is reported. Based on different solubility of sulfur in different solvents, nano-sulfur/MWCNTs composite was prepared by solvents exchange method. The composite was characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The modified MWCNTs are considered that not only acts as a conducting material, but also a matrix for sulfur. The electrochemical performance of the nano-sulfur/MWCNTs composite was tested. The results indicated that nano-sulfur/MWCNTs composite had the specific capacity of 1380 mAh g−1, 1326 mAh g−1 and 1210 mAh g−1 in the initial cycle at 100 mA g−1, 200 mA g−1 and 300 mAh g−1 discharge rates respectively, and remained a reversible capacity of 1020 mAh g−1, 870 mAh g−1 and 810 mAh g−1 after 30 cycles. The electrochemical performances confirm that the modified MWCNTs as sulfur-fixed matrix show better ability than any other carbon in cathode of Li/S batteries that had been reported.  相似文献   

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