Influence of functionalization on properties of MWCNT-epoxy nanocomposites

The effects of various functionalized multi-walled carbon nanotubes (MWCNTs) on morphological, thermal, and mechanical properties of an epoxy based nanocomposite system were investigated. Chemical functionalization of MWCNT by oxidation (MWCNT-COOH) and direct-fluorination (MWCNT-F) were confirmed by FTIR, Raman spectroscopy, and TGA. Utilizing in situ polymerization, 1 wt% loading of MWCNT was used to prepare epoxy-based nanocomposites. Compared to the neat epoxy system, nanocomposites prepared with MWCNT-COOH showed 25.5% increase in ultimate flexural strength and 54.8% increase in flexural modulus. A decrease in strength was observed for the MWCNT-F nanocomposites. The premature degradation was attributed to a presumable catalyzation by hydrofluoric acid, HF, which evolved from the MWCNT-F during the curing process. However, only the MWCNT-F nanocomposites showed 22% increase in thermal properties (T_g). All nanophased systems showed increase in storage modulus.     

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.     

New development of self-damping MWCNT composites

Epoxy resin modified with nanofillers cannot be used alone for high performance structural applications due to their low-mechanical properties. Therefore, the objective of this work is to hybridize unidirectional and quasi-isotropic glass fiber composite laminates with 1.0 wt% multi-walled carbon nanotubes (MWCNTs). Results from flexural and damping characterizations showed that the flexural strength and modulus, storage modulus, and damping ratio of MWCNT/E nanocomposite are improved by about 7% ± 1.5% compared to neat epoxy. The enhancement in the flexural strength of quasi-isotropic laminate (20.7%) is about ten times higher than that for unidirectional laminate (2.1%). The flexural moduli of the nano-hybridized laminates are reduced by about 7.5–10.8%. Accordingly, the ultimate failure strain and damping properties are evidently improved. The improvement in damping ratio in some cases is about 100%. The high correlation coefficient (0.9995) between flexural and storage moduli suggests using the dynamic nondestructive tests for evaluation the elastic properties of composites.     

Effect of surface functionalization on mechanical properties and decomposition kinetics of high performance polyetherimide/MWCNT nano composites

In this investigation, Polyetherimide (PEI) reinforced with multi-walled carbon nanotube (MWCNT) using novel melt blending technique. Surface of MWCNTs are modified by acid treatment as well as by plasma treatment. PEI nano composites with 2 wt% treated MWCNT shows about 15% improvement in mechanical properties when compared to unfilled PEI. The thermal decomposition kinetics of PEI/MWCNT nano composites has been critically analyzed by using Coats – Redfern model. The increase in activation energy for thermal degradation by 699 kJ/mol for 2 wt% MWCNT implies improvement in the thermal properties of PEI. Studies under Fourier Transform Infrared Spectroscopy (FTIR) and Transmission Electron Microscopy (TEM) depict significant interfacial adhesion with uniform dispersion of MWCNT in polymer matrix due to surface functionalization. 0.5 wt% chemically modified MWCNT shows typical alignment of MWCNT. There is a significant improvement in mechanical properties and thermal properties for surface functionalized MWCNT reinforced.     

Influence of nanotube content on the mechanical and thermo-mechanical behaviour of –COOH functionalized MWNTs/epoxy composites

Functionalized multi-wall carbon nanotubes (MWNTs) with carboxylic acid group (–COOH) have been utilized for the preparation of epoxy nanocomposites. Composites were synthesized using three different wt% (0.5, 0.75 and 1) of MWNTs via the solution mixing technique followed by ultrasonication. Mechanical and thermo-mechanical properties of the fabricated composites have been experimented for the suitability of this material in a variety of structural applications. The flexural modulus, strength, hardness, impact strength and storage modulus increased upon increasing MWNTs contents. Best results have been observed in nanocomposites with 0.75 wt% nanotubes loading, which showed 101, 166 and 61% enhancement in the flexural modulus, hardness and storage modulus, respectively, compared to neat epoxy. Achievement of uniform dispersion and hence formation of improved interface between nanotubes and epoxy was the reason behind the maximum enhancement at this wt%, which is further evidenced by the fracture surface morphology obtained from microscopical investigations.     

Thermal and mechanical properties of phenolic-based composites reinforced by carbon fibres and multiwall carbon nanotubes

The thermal, mechanical and ablation properties of carbon fibre/phenolic composites filled with multiwall carbon nanotubes (MWCNTs) were investigated. Carbon fibre/phenolic/MWCNTs were prepared using different weight percentage of MWCNTs by compression moulding. The samples were characterized by scanning electron microscopy (SEM), flexural tests, thermal gravimetric analysis and oxyacetylene torch tests. The thermal stability and flexural properties of the nanocomposites increased by increasing MWCNTs content (wt% ⩽1), but they decreased when the content of MWCNTs was 2 wt%. The linear and mass ablation rates of the nanocomposites after modified with 1 wt% MWCNTs decreased by about 80% and 52%, respectively. To investigate the material post-test microstructure, a morphological characterization was carried out using SEM. It was shown that the presence of MWCNTs in the composite led to the formation of a strong network char layer without any cracks or opening.     

Influence of ultrasonic dual mixing on thermal and tensile properties of MWCNTs-epoxy composite

Multiwalled carbon nanotubes (MWCNTs) reinforced epoxy based composites were fabricated by using an innovative ultrasonic dual mixing (UDM) process consists of ultrasonic mixing with simultaneous magnetic stirring. The effect of addition of varying amount of MWCNTs on thermal stability and tensile properties of the epoxy based composite has been investigated. It is found that the thermal stability, tensile strength and toughness of the epoxy base improves with the increase of MWCNTs addition up to 1.5 wt.% and UDM processing at certain capacity of the system. Tensile tests and thermal gravimetric analysis (TGA) were performed on each group of composites containing different amount of MWCNTs to determine their mechanical and thermal properties respectively. The dispersion of 1.5 wt.% MWCNTs fillers in epoxy nanocomposites was studied by transmission electron microscopy (TEM) as well as by field emission scanning electron microscopy (FESEM) applied on their tensile fracture surface.     

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.     

Effect of block-copolymer dispersants on properties of carbon nanotube/epoxy systems

The effects of the addition of eight different block copolymers on the dispersion stability of multi-walled carbon nanotubes (MWCNTs) are reported. Suspensions of CNTs in different components of an epoxy system have been prepared using a tip sonicator and different amounts of block copolymers. The resistance to sedimentation of MWCNTs in various media was systematically investigated by using a centrifugation technique. Block copolymers that result in dispersions of MWCNTs in epoxy and hardener stable for more than 1 week have been obtained. Dispersions using a single or a combination of two different dispersing agents have been used for the fabrication of MWCNT nanocomposites. The effect of different preparation routes and use of block copolymers on the tensile properties and surface resistivity of the composites have been evaluated. The results obtained have been related with the dispersion stability of the MWCNTs in the epoxy components.     

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.     

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.     

Effect of chemical functionalization of multi-walled carbon nanotubes with 3-aminopropyltriethoxysilane on mechanical and morphological properties of epoxy nanocomposites

Nanocomposites based on epoxy resin and different weight percentages of unmodified, oxidized, and silanized multi-walled carbon nanotubes (MWCNTs) were prepared by cast molding method. Effects of MWCNTs content on the flexural properties were examined. The results showed that as the loading of the MWCNTs increased, improved flexural strength and flexural modulus were observed. The mechanical properties decreased when the MWCNTs content exceeded 0.2 wt.% due to agglomeration of MWCNTs. These results prove the effect of functionalization on the interfacial adhesion between epoxy and MWCNTs. This was further confirmed by morphology study of fractured surfaces of nanocomposites by SEM and TEM.     

Improving the mechanical properties of epoxy using multiwalled carbon nanotubes functionalized by a novel plasma treatment

Achieving both uniform dispersion and good interfacial adhesion have been long-term challenges in optimizing the properties of carbon nanotube reinforced polymer nanocomposites. A novel and effective plasma method, which combines continuous and pulsed plasma modes in a nitrogen and hydrogen gas mixture (15% H₂), has been developed to better meet this need. It has yielded high levels of primary amines on the surface of multiwalled carbon nanotubes which improved their dispersion and interfacial bonding with an epoxy resin. By adding just 0.1 wt% of these nanotubes to Bisphenol F epoxy resin, the mechanical properties of the nanocomposites, from nano to macro, were significantly improved. Nanoindentation tests showed that the hardness and elastic modulus increased by 40% and 19%, respectively, using the functionalized nanotubes. Macro-mechanical properties from thermo-mechanical and flexural analysis were also enhanced, with a nearly 40% improvement in toughness.     

Poly (butylene terephthalate)/silica nanocomposites prepared from cyclic butylene terephthalate

Poly (butylene terephthalate) (PBT)/silica nanocomposites were compounded from cyclic butylene terephthalate (CBT) resin with very low melt viscosity via high-speed stirring and subsequent in situ polymerization. The effect of silica nanoparticles on the properties of CBT and its polymer composites has been studied. It was shown that the well-dispersed silica nanoparticles, even in small content (1–2 wt.%), result in the dramatic extension of the polymerization process of CBT resin. The flexural properties of polymerized PBT nanocomposites, including modulus, yield strength and failure strain, was improved significantly with the incorporation of silica nanoparticles.     

Scavenging phenomenon and improved electrical and mechanical properties of polyaniline–divinylbenzene composite in presence of MWCNT

A semi-doped polyaniline (PANI)–dodecylbenzenesulfonic acid (DBSA) complex is added with a suspension of multiwall carbon nanotubes (MWCNT)–divinylbenzene (DVB) to prepare PANI–MWCNT based thermosetting conductive resin system. Firstly, unreinforced nanocomposites with various loading of MWCNT are prepared. Continuous improvement in the electrical conductivity is observed with increasing MWCNT loading in the composite, while improvement in the mechanical properties is observed only up to 0.2 wt% MWCNT loading. On further MWCNT loading, the decrease in mechanical properties is observed. Flexural strength increased by 18% with 0.2 wt% of MWCNT in the unreinforced nanocomposite while electrical conductivity increased continuously to 0.68 S/cm (at 0.5 wt% of MWCNT loading) from 0.25 S/cm (neat sample). DSC and TGA analysis show that MWCNT effectively contributed to enhance the scavenging effect of PANI, affecting degree of DVB polymerization at higher loading of MWCNT. Samples were characterized by FTIR analysis. DMA analysis is also performed to understand the mechanical behavior of the cured unreinforced nanocomposite under dynamic loading. SEM observation has been employed to understand the dispersion behavior of MWCNT into the matrix. PANI-wrapping behavior on MWCNT is observed from the SEM images. Wrapping of PANI on MWCNT increased doping state and surface area of PANI which subsequently contribute to the increased scavenging behavior of PANI at higher MWCNT loading. A structural thermosetting nanocomposite with electrical conductivity of 0.68 S/cm, flexural modulus of 1.87 GPa and flexural strength up to 35 MPa is prepared. In addition, PANI–DBSA/DVB matrix with MWCNT is also used to impregnate carbon fabrics to prepare highly conductive CFRPs. A CFRP with 1.67 S/cm electrical conductivity in through-thickness direction and 328 MPa flexural strength is obtained with the addition of 0.2 wt% MWCNT into the resin system.     

Effects of stretching on mechanical properties of aligned multi-walled carbon nanotube/epoxy composites

Composites based on epoxy resin and differently aligned multi-walled carbon nanotube (MWCNT) sheets have been developed using hot-melt prepreg processing. Aligned MWCNT sheets were produced from MWCNT arrays using the drawing and winding technique. Wavy MWCNTs in the sheets have limited reinforcement efficiency in the composites. Therefore, mechanical stretching of the MWCNT sheets and their prepregs was conducted for this study. Mechanical stretching of the MWCNT sheets and hot stretching of the MWCNT/epoxy prepregs markedly improved the mechanical properties of the composites. The improved mechanical properties of stretched composites derived from the increased MWCNT volume fraction and the reduced MWCNT waviness caused by stretching. With a 3% stretch ratio, the MWCNT/epoxy composites achieved their best mechanical properties in this study. Although hot stretching of the prepregs increased the tensile strength and modulus of the composites considerably, its efficiency was lower than that of stretching the MWCNT sheets.     

The thermal conductivity of embedded nano-aluminum nitride-doped multi-walled carbon nanotubes in epoxy composites containing micro-aluminum nitride particles

Amino-functionalized nano-aluminum nitride (nano-AlN) particles were doped onto the surfaces of chlorinated multi-walled carbon nanotubes (MWCNTs) to act as fillers in thermally conducting composites. These synthesized materials were embedded in epoxy resin. Then, the untreated micro-aluminum nitride (micro-AlN) particles were added to this resin, whereby the composites filled with nano-AlN-doped MWCNTs (0, 0.5, 1, 1.5, 2 wt%) and micro-AlN (25.2, 44.1, 57.4 vol%) were fabricated. As a result, the thermal diffusivity and conductivity of all composites continuously improved with increasing nano-AlN-doped MWCNT content and micro-AlN filler loading. The thermal conductivity reached its maximum, which was 31.27 times that of the epoxy alone, when 2 wt% nano-AlN-doped MWCNTs and 57.4 vol% micro-AlN were added to the epoxy resin. This result is due to the high aspect ratio of the MWCNTs and the surface polarity of the doped nano-AlN and micro-AlN particles, resulting in the improved thermal properties of the epoxy composite.     

Synthesis of polyaniline/multi-walled carbon nanotube nanocomposites in water/oil microemulsion

A water/oil microemulsion system having been successfully used for synthesizing polyaniline(PANi) nanoparticles, was employed for preparing PANi/multi-walled carbon nanotube (MWCNT) nanocomposites via in situ chemical oxidative polymerization. The structures and the electrical property of PANi/MWCNT nanocomposites were also studied. The studies showed that PANi could coat MWCNTs to form nanocables with core-shell structure, and the backbone structure of PANi was not damaged by the introduction of MWCNTs. The conductivities of PANi/MWCNT nanocomposites were higher than that of PANi. Moreover, a model was supposed to be used for describing a PANi/MWCNT nanocable formation by in situ microemulsion polymerization.     

Fracture mechanisms of epoxy filled with ozone functionalized multi-wall carbon nanotubes

This work focused on the fracture mechanisms and reinforcing effects of ozone-treated multi-walled carbon nanotubes (MWCNTs) in epoxy matrix. Ozone functionalization of MWCNTs was found to be of help for a better dispersion and stronger interfacial bonding with epoxy matrix, which in turn improve the strength and fracture toughness of the resin. The MWCNT/epoxy composites showed complicated failure modes than the conventional fibrous composites, which have been quantitatively investigated and correlated with the fracture toughness of the nanocomposites studied.     

Preparation,characterization and properties of polycaprolactone diol-functionalized multi-walled carbon nanotube/thermoplastic polyurethane composite

Multi-walled carbon nanotubes (MWCNTs) were chemically functionalized to prepare thermoplastic polyurethane (PU) composites with enhanced properties. In order to achieve a high compatibility of functionalized MWCNTs with the PU matrix, polycaprolactone diol (PCL), as one of PU’s monomers, was selectively grafted on the surface of MWCNTs (MWCNT–PCL), while carboxylic acid groups functionalized MWCNTs (MWCNT–COOH) and raw MWCNTs served as control. Both MWCNT–COOH and MWCNT–PCL improved the dispersion of MWCNTs in the PU matrix and interfacial bonding between them at 1 wt% loading fraction. The MWCNT–PCL/PU composite showed the greatest extent of improvement, where the tensile strength and modulus were 51.2% and 33.5% higher than those of pure PU respectively, without sacrificing the elongation at break. The considerable improvement in both mechanical properties and thermal stability of MWCNT–PCL/PU composite should result from the homogeneous dispersion of MWCNT–PCL in the PU matrix and strong interfacial bonding between them.