Oxygen Barrier of Multiwalled Carbon Nanotube/Polymethyl Methacrylate Nanocomposites Prepared by in situ Method

Multiwalled carbon nanotubes (MWCNTs)/poly(methyl methacrylate) (PMMA) nanocomposites were prepared by ultrasonic assisted emulsifier free emulsion polymerization technique with variable concentration of functionalized carbon nanotubes. MWCNTs were functionalized with H 2 SO 4 and HNO 3 with continuing sonication and polished by H 2 O 2 . The appearance of Fourier transform infrared absorption bands in the PMMA/MWCNT nanocomposites showed that the functionalized MWCNT interacted chemically with PMMA macromolecules. The surface morphology of functionalized MWCNT and PMMA/MWCNT nanocomposites were studied by scanning electron microscopy. The dispersion of MWCNT in PMMA matrix was evidenced by high resolution transmission electron microscopy. The oxygen permeability of PMMA/MWCNT nanocomposites gradually decreased with increasing MWCNT concentrations.     

Properties of polycarbonate (PC)/multi-wall carbon nanotube (MWCNT) nanocomposites prepared by melt blending

This investigation deals with an easy method to develop electrical conductivity in polycarbonate (PC)/multi-wall carbon nanotube (MWCNT) nanocomposites with low loading of MWCNT. This was achieved by melt-blending of in-situ bulk polymerized low molecular weight poly(methyl methacrylate) (PMMA)/MWCNT nanocomposites and PC in various compositions at 280 degrees C in internal mixer. Differential scanning calorimetry (DSC) study showed single Tg in (85/15 w/w) PC/PMMA blend, indicating miscibility of PC and PMMA in the blend. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) studies of the melt-blended PC/PMMA/MWCNT nanocomposites revealed homogeneous dispersion and distribution of MWCNTs in PC matrix. Finally, through optimizing the blending composition of PC and PMMA/MWCNT nanocomposites, electrical conductivity of 3.74 x 10(-7) S x cm(-1) was achieved in the (85/15 w/w) PC/PMMA/MWCNT nanocomposites with the MWCNTs loading as low as approximately 0.37 wt%. Storage modulus of PC was found to increase significantly in presence of small amount (0.37 wt%) of MWCNTs in the nanocomposites.     

Influence of multiwall carbon nanotube functionality and loading on mechanical properties of PMMA/MWCNT bone cements

Poly (methyl methacrylate) (PMMA) bone cement—multi walled carbon nanotube (MWCNT) nanocomposites with weight loadings ranging from 0.1 to 1.0 wt% were prepared. The MWCNTs investigated were unfunctionalised, carboxyl and amine functionalised MWCNTs. Mechanical properties of the resultant nanocomposite cements were characterised as per international standards for acrylic resin cements. These mechanical properties were influenced by the type and wt% loading of MWCNT used. The morphology and degree of dispersion of the MWCNTs in the PMMA matrix at different length scales were examined using field emission scanning electron microscopy. Improvements in mechanical properties were attributed to the MWCNTs arresting/retarding crack propagation through the cement by providing a bridging effect and hindering crack propagation. MWCNTs agglomerations were evident within the cement microstructure, the degree of these agglomerations was dependent on the weight fraction and functionality of MWCNTs incorporated into the cement.     

Properties of poly(lactic acid)/montmorillonite/carbon nanotubes nanocomposites: determination of percolation threshold

Incorporation of rigid nanoparticles is the most effective means of improving polymer properties. Montmorillonite (MMT) and multi-walled carbon nanotubes (MWCNTs) are legendary in this field for their individual exceptional properties. A synergistic phenomenon is induced between these two particles when they are simultaneously incorporated into polymers. At a definite nanofillers concentration, called the percolation threshold, there is a sudden change in nanocomposite properties due to the formation of a 3D-structured network of the nanoparticles within the matrix. In this work, the properties of poly(lactic acid) (PLA) nanocomposites filled with different fractions of MMT/MWCNTs hybrid (0.5–2.0 wt%) were analyzed. In particular, the percolation threshold of the MMT/MWCNTs hybrid was uniquely identified by differential scanning calorimetry, thermogravimetric analysis and dynamic mechanical thermal analysis. The structural studies by X-ray diffraction and Fourier-transform infrared spectroscopy were also associated with the percolation threshold of MMT/MWCNTs in PLA. At 1.0 wt% MMT/MWCNTs concentration, the complete exfoliation of the particles was maintained, and the thermal characteristics such as glass transition, crystallization and melting temperatures reached their plateau at this hybrid concentration. Moreover, the thermal degradation and viscoelastic parameters showed their peak values at this critical point, which is correlated with the formation of the percolation threshold within the matrix. The morphological studies confirmed the homogeneous dispersion of MMT/MWCNTs in PLA up to a concentration of 1.0 wt%. At 2.0 wt% MMT/MWCNTs, few aggregations occurred in the PLA-based composite, confirming that the percolation threshold was formed at a lower concentration of MMT/MWCNTs nanoparticles.

     

Dispersion characteristics and properties of poly(methyl methacrylate)/multi-walled carbon nanotubes nanocomposites

The preparation, characterization, and properties of poly(methyl methacrylate) (PMMA)/multi-walled carbon nanotubes (MWCNTs) nanocomposites are described. Nanocomposites have been prepared by melt-blending in a batch mixer. Both unmodified and surface modified MWCNTs have been used for the nanocomposites preparation. Using both unmodified and modified MWCNTs, the effect of surface modification in nanocomposites is investigated by focusing on three major aspects: dispersion characteristics, mechanical properties, and electrical conductivity measurements. Dispersion of the MWCNTs in the PMMA matrix is examined by scanning and transmission electron microscopy that revealed a homogeneous distribution-dispersion of MWCNTs in the PMMA matrix for both unmodified and modified MWCNTs. Thermomechanical behavior is studied by dynamic mechanical analyzer and results showed a substantial improvement in the mechanical properties of PMMA in conjunction to an increase in the elastic behavior. The tensile properties of neat PMMA moderately improved after nanocomposites preparation with both modified and unmodified MWCNTs, however, electrical conductivity of neat PMMA significantly improved after nanocomposites preparation with 2 wt% unmodified MWCNTs. For example, the through plane conductivity increased from 3.6 x 10(-12) S x cm(-1) for neat PMMA to 3.6 x 10(-9) S x cm(-1) for nanocomposite. The various property measurements have been conducted and results have shown that, in overall, surface modifications have very little or no effect on final properties of neat PMMA.     

Hybrid Composite Using Natural Filler and Multi-Walled Carbon Nanotubes (MWCNTs)

This paper presents an experimental study on the development of hybrid composites comprising of multi-walled carbon nanotubes (MWCNTs) and natural filler (oil palm shell (OPS) powder) within unsaturated polyester (UP) matrix. The results revealed that the dispersion of pristine MWCNTs in the polymer matrix was strongly enhanced through use of the solvent mixing method assisted by ultrasonication. Four different solvents were investigated, namely, ethanol, methanol, styrene and acetone. The best compatibility with minimum side effects on the curing of the polyester resin was exhibited by the styrene solvent and this produced the maximum tensile and flexural properties of the resulting nanocomposites. A relatively small amount of pristine MWCNTs well dispersed within the natural filler polyester composite was found to be capable of improving mechanical properties of hybrid composite. However, increasing the MWCNT amount resulted in increased void content within the matrix due to an associated rapid increase in viscosity of the mixture during processing. Due to this phenomenon, the maximum tensile and flexural strengths of the hybrid composites were achieved at MWCNT contents of 0.2 to 0.4 phr and then declined for higher MWCNT amounts. The flexural modulus also experienced its peak at 0.4 phr MWCNT content whereas the tensile modulus exhibited a general decrease with increasing MWCNT content. Thermal stability analysis using TGA under an oxidative atmosphere showed that adding MWCNTs shifted the endset degradation temperature of the hybrid composite to a higher temperature.     

Synergistic effects in network formation and electrical properties of hybrid epoxy nanocomposites containing multi-wall carbon nanotubes and carbon black

Epoxy nanocomposites including multi-wall carbon nanotubes (MWCNT) and carbon black (CB) were produced and investigated by means of electrical conductivity measurements and microscopical analysis. Varying the weight fraction of the nanoparticles, electrical percolation behaviour was studied. Due to synergistic effects in network formation and in charge transport the inclusion of both MWCNT and CB in the epoxy matrix leads to an identical electrical behaviour of this ternary nanocomposite system compared to the binary MWCNT-epoxy system. For both types of nanocomposites an electrical percolation threshold of around 0.025 wt% and 0.03 wt% was observed. Conversely, the binary CB nanocomposites exhibit a three-times higher percolation threshold of about 0.085 wt%. The difference between the binary MWCNT-epoxy and the ternary CB/MWCNT-epoxy in electrical conductivity at high filler concentrations (e.g. 0.5 wt%) turns out to be less than expected. Thus, a considerable amount of MWCNTs can be replaced by CB without changing the electrical properties.     

Comparison of rheological and electrical percolation phenomena in carbon black and carbon nanotube filled epoxy polymers

Epoxy nanocomposite suspensions including multi-wall carbon nanotubes (MWCNTs) and carbon black (CB) were produced and investigated by means of combined rheological and electrical analysis. The rheological percolation behaviour was compared to the electrical percolation behaviour. Due to similar dynamic agglomeration mechanisms the difference between the rheological and the electrical percolation threshold in the cured state is identical for MWCNT and CB filled systems. Non-covalent matrix–nanoparticle interactions in uncured epoxy suspensions are negligible since the onset of electrical and rheological percolation in the uncured state coincidence. Furthermore, the electrical percolation threshold in the cured state is always lower than in the uncured state because of the high tendency of CB and MWCNTs to form conductive networks during curing. The difference between rheological and electrical percolation threshold is dependent on the curing conditions. Thus, the rheological percolation threshold can be considered as an upper limit for the electrical percolation threshold in the cured state. Due to the formation of co-supporting networks multi-filler (MWCNTs and CB) suspensions exhibit a similar rheological behaviour as the binary MWCNT suspensions. For both types of suspensions a rheological percolation threshold of around 0.2 and 0.25 wt% was determined. Conversely, the binary CB nanocomposites exhibit a four-times higher percolation threshold of about 0.8 wt%. The difference between the binary MWCNT suspension and the ternary CB/MWCNT suspension in storage shear modulus at high filler concentrations (~0.8 wt%) turns out to be less than expected. Thus, synergistic effects in network formation are already present in the epoxy suspension and get more pronounced during curing.     

Filler dispersion and electrical properties of polyamide 12/MWCNT-nanocomposites produced in reactive extrusion via anionic ring-opening polymerization

The reactive extrusion of lauryl lactam to polyamide 12 (PA12) of controlled molar mass was successfully performed in a microcompounder. The maximum residual monomer content was less than 1%. The in-situ polymerization in the presence of 1–5 wt.% multiwalled carbon nanotubes (MWCNTs) was studied and the processing conditions were optimized with respect to the electrical resistivity and MWCNT dispersion. Runs which yielded in higher molar mass PA12 resulted in better dispersion of MWCNTs, whereas nanocomposites with lower molar mass PA12 had lower electrical percolation thresholds (MWCNT concentration ∼1 wt.%). A high screw speed of 200 rpm was identified to cause best dispersion and the lowest percolation threshold.     

Carbon nanotube modification using gum arabic and its effect on the dispersion and tensile properties of carbon nanotubes/epoxy nanocomposites

In this study, the effects of a MWCNT treatment on the dispersion of MWCNTs in aqueous solution and the tensile properties of MWCNT/epoxy nanocomposites were investigated. MWCNTs were treated using acid and gum arabic, and MWCNT/epoxy nanocomposites were fabricated with 0.3 wt.% unmodified, oxidized and gum-treated MWCNTs. The dispersion states of the unmodified, oxidized, and Gum-treated MWCNTs were characterized in distilled water. The tensile strengths and elastic modulus of the three nanocomposites were determined and compared. The results indicated that the gum treatment produced better dispersion of the MWCNTs in distilled water and that gum-treated MWCNT/epoxy nanocomposites had a better tensile strength and elastic modulus than did the unmodified and acid-treated MWCNT/epoxy nanocomposites. Scanning electron microscope examination of the fracture surface showed that the improved tensile properties of the gum-treated MWCNT/epoxy nanocomposites were attributed to the improved dispersion of MWCNTs in the epoxy and to interfacial bonding between nanotubes and the epoxy matrix.     

Controlling the shapes and electrical conductivities of polyaniline-wrapped MWCNTs

Nanocomposites of carbon nanotubes with polyaniline (PANI) constitute promising conducting nanomaterials, due to their ease of synthesis, electrical conductivity, and environmental stability. Variously shaped multi-walled carbon nanotube (MWCNT)-PANI nanocomposites were synthesized, and their electrical conductivities were compared. This study shows that new synthetic methods were able to control the shapes and electrical conductivities of MWCNT-PANI nanocomposites. The shapes of the MWCNT-PANI nanocomposites were changed by altering the reactant concentrations and the sequence of adding the initiator, ammonium persulfate (APS). The use of surface-modified MWCNTs instead of pristine MWCNTs is also an important factor determining the shapes of the nanocomposites. It was found that the electrical conductivity is strongly dependent on the shape and PANI content. The electrical conductivities of the MWCNT-PANI nanocomposites increased when the PANI/MWCNT ratio was decreased. The nanocomposites were characterized via field emission transmission electron microscopy (FE-TEM), Fourier-transform infrared (FT-IR) and ultraviolet-visible (UV-Vis) spectroscopy, and elementary analysis of the MWCNT-PANI nanocomposites.     

Preparation and properties of chitosan nanocomposite films reinforced by poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) treated carbon nanotubes

Carbon nanotube-based nanocomposites of chitosan were successfully prepared by a simple solution-evaporation method. Multiwalled carbon nanotubes (MWCNTs) were treated by poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate)(PEDOT-PSS) in water before mixed with a chitosan solution to improve the dispersion of MWCNTs and interfacial compatibility between MWCNTs and chitosan. The morphological and mechanical properties of the prepared PEDOT-PSS/MWCNT/chitosan nanocomposites have been characterized with field emission scanning electron microscopy (FESEM) and tensile tests. MWCNTs were observed to be homogeneously dispersed throughout the chitosan matrix. As compared with the neat chitosan, the tensile strength and modulus of the nanocomposite were greatly improved by about 61% and 34%, respectively, with incorporation of only 0.5 wt.% of MWCNTs into the chitosan matrix. The comparison of mechanical properties for PEDOT-PSS/MWCNT/chitosan and pristine MWCNT/chitosan nanocomposites has been made. The hardness of the nanocomposites was also evaluated by nanoindentation.     

Widely dispersed PEI-based nanocomposites with multi-wall carbon nanotubes by blending with a masterbatch

High performance poly(etherimide) (PEI)-based nanocomposites (PNs) with multi-walled carbon nanotubes (MWCNT) were obtained via melt mixing. To achieve this, PEI was mixed with a well-dispersed commercial poly(butylene terephthalate) (PBT)/MWCNT master-batch in an attempt to transfer the dispersed MWCNTs to a PEI matrix. A broad and homogeneous dispersion of MWCNTs throughout the PEI-based matrix was obtained. The electrical percolation threshold (p_c) was reached at only 1 wt.% MWCNT. This p_c showed a power law dependence of conductivity on filler concentration, with a critical exponent of 1.92, which indicates that a three dimensional percolated structure was achieved. The glass transition temperature and the pressure at the output end of the extruder decreased when the master-batch was added, indicating that the processability of PEI was improved. In addition to this, the modified PEI-based PNs presented ductile behaviour and an ameliorated (12% with 5 wt.% MWCNT) elastic modulus compared with pure PEI.     

Microspherical poly(methyl methacrylate)/multiwalled carbon nanotube composites prepared via in situ dispersion polymerization

In this study, microspherical poly(methyl methacrylate)/multi-walled carbon nanotube (PMMA/ MWCNT) composites were directly prepared by in situ dispersion polymerization using poly (N-vinylpyrrolidone) in methanol media. PMMA/MWCNT microspheres having a diameter of 2.6 approximately 3.9 microm and a molecular weight of 58,000 approximately 65,000 g/mol with a 15.7 approximately 19.5% coefficient of variation (Cv) were synthesized. The morphology of the synthesized composite was investigated using scanning electron microscopy and transmission electron microscopy. The experimental results demonstrated that MWCNTs are well dispersed and embedded in the final PMMA/MWCNT microspheres. The prepared PMMA/MWCNT microspheres were investigated in terms of their capacity to serve as an electrorheological (ER) materials.     

Reducing resistivity of polyamide-6/multi-walled carbon nanotube composites by adding ultra-fine rubber particles on account of non-volume exclusion effect

The volume resistivity of polyamide-6(PA6)/multi-walled carbon nanotube (MWCNT) composites was found to be further reduced by adding a kind of ultra-fine rubber particle (URP) with average diameter of 150 nm due to non-volume exclusion effect. With the addition of 16 phr URP, the percolation threshold of PA6/MWCNT composites was reduced from 6 phr MWCNTs to 3 phr. Besides, at a constant loading of 4 phr MWCNTs, increase of URP loading led to two changes and a plateau for the volume resistivity of composites. The morphological observations of composites revealed that the decrease of volume resistivity was attributed to both homogenous dispersion and stretching of MWCNTs in PA6. The mechanism on better dispersion and stretching of MWCNTs with the help of URP was also given.     

Effect of maleic anhydride modified MWCNTs on the morphology and dynamic mechanical properties of its PMMA composites

This study successfully grafted multiwalled carbon nanotubes (MWCNTs) with maleic anhydride (Mah-g-MWCNTs) via Friedel–Crafts acylation with the aluminum chloride catalyst (AlCl₃), investigated by Raman and TGA analysis. The covalent bonds and carboxylic groups of maleic anhydride provided additional active species, improving adhesion between the MWCNTs and poly(methyl methacrylate) (PMMA). This investigation also studied the morphology and dynamic mechanical properties of pristine MWCNTs (P-MWCNTs) and modified MWCNTs (Mah-g-MWCNTs) reinforced with PMMA. Findings show a homogeneous distribution of MWCNTs throughout the matrix for Mah-g-MWCNTs/PMMA composites, as revealed by transmission electron microscope (TEM). The addition of both MWCNTs influenced the molecular arrangement of the PMMA matrix and also increased the dynamic mechanical properties of MWCNTs/PMMA composites. Glass transition temperature (Tg) and storage moduli (E′) of the Mah-g-MWCNTs/PMMA composites increased significantly comparing with P-MWCNTs/PMMA composites, attributed to improved interfacial adhesion between the reinforcement and the matrix. DMA studies revealed that adding 4.76 wt% Mah-g-MWCNTs into PMMA generates a 184% enhancement in the storage modulus and a 19 °C increase in Tg. However, adding 4.76 wt% P-MWCNTs into PMMA only generates 108% enhancement in the storage modulus and a 14 °C increase in Tg.     

Poly(3- hydroxybutyrate)/Bioglass(®) composite films containing carbon nanotubes

Poly(3hydroxybutyrate) (P(3HB))/Bioglass(?)?composites incorporating multiwalled carbon nanotubes (MWCNTs) have been successfully prepared by the solvent casting technique. The microstructure, electrical properties and bioactivity of the composites were characterized using scanning electron microscopy, x-ray diffraction and current-voltage measurements. Different concentrations of MWCNTs were used to determine their effect on the electrical properties of the composites. MWCNTs and Bioglass(?) particles were found to be homogeneously dispersed throughout the P(3HB) matrix. The electrical resistance of the composite samples decreased on increasing the MWCNT concentration, as expected. An in vitro degradation study in simulated body fluid (SBF) was carried out on composite samples. The formation of hydroxyapatite on the surfaces of P(3HB)/Bioglass(?)/MWCNT composite films was confirmed after two months of immersion in SBF. This hydroxyapatite layer was not formed on the neat polymeric films and on composites containing MWCNTs only (without Bioglass(?)). It was found that the presence of MWCNTs did not hinder the bioactivity of the Bioglass(?) particles, as confirmed by SEM and XRD studies on composite samples.     

Fabrication of alizarin red S/multi-walled carbon nanotube nanocomposites and their application in hydrogen peroxide detection

In this work, an easy and effective method to synthesize alizarin red S/multi-walled carbon nanotube (ARS/MWCNT) nanocomposites based on the π–π stacking non-covalent interactions between ARS and MWCNTs was introduced. The characters of ARS/MWCNT nanocomposites were investigated by Fourier transformation infrared spectroscopy, UV–Vis spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscope, and electrochemical techniques. ARS tightly coating on MWCNTs surface makes the nanocomposites good dispersibility in water and excellent electrochemical activity. Because of the combination of the excellent electroactivity of ARS and the unique properties of MWCNTs, ARS/MWCNT nanocomposites-modified glassy carbon electrode exhibits a good response to the reduction of hydrogen peroxide and takes on a promising prospect of the practical application in electrochemical sensors field.     

Fabrication and characterization of carbon nanotube reinforced poly(methyl methacrylate) nanocomposites

Multiwall carbon nanotube (CNT) reinforced poly(methyl methacrylate) (PMMA) nanocomposites have been successfully fabricated with melt blending. Two melt blending approaches of batch mixing and continuous extrusion have been used and the properties of the derived nanocomposites have been compared. The interaction of PMMA and CNTs, which is crucial to greatly improve the polymer properties, has been physically enhanced by adding a third party of poly(vinylidene fluoride) (PVDF) compatibilizer. It is found that the electrical threshold for both PMMA/CNT and PMMA/PVDF/CNT nanocomposites lies between 0.5 to 1 wt% of CNTs. The thermal and mechanical properties of the nanocomposites increase with CNTs and they are further increased by the addition of PVDF For 5 wt% CNT reinforced PMMA/PVDF/CNT nanocomposite, the onset of decomposition temperature is about 17 degrees C higher and elastic modulus is about 19.5% higher than those of neat PMMA. Rheological study also shows that the CNTs incorporated in the PMMA/PVDF/CNT nanocomposites act as physical cross-linkers.     

聚偏氟乙烯/碳纳米管纳米复合材料的制备和表征

采用超声波分散法制备了聚偏氟乙烯(PVDF)/多壁碳纳米管(MWCNT)复合材料。利用扫描电子显微镜、差示扫描量热法和傅立叶变换红外光谱等方法研究了复合材料的形态,考察了MWCNT用量对复合材料结晶行为和力学性能的影响。结果表明,通过超声处理,PVDF和MWCNTs之间产生了相互作用,复合体以球状的形式存在。MWCNTs的引入导致具有压电性的β相形成和屈服强度的提高。根据实验结果,对PVDF/MWCNT复合球体和β相的形成机理提出了可能的解释。