Effect of dispersion conditions on the thermo-mechanical and toughness properties of multi walled carbon nanotubes-reinforced epoxy

In this work, multi wall carbon nanotubes (MWCNTs) dispersed in a polymer matrix have been used to enhance the thermo-mechanical and toughness properties of the resulting nanocomposites. Dynamic mechanical analysis (DMA), tensile tests and single edge notch 3-point bending tests were performed on unfilled, 0.5 and 1 wt.% carbon nanotube (CNT)-filled epoxy to identify the effect of loading on the aforementioned properties. The effect of the dispersion conditions has been thoroughly investigated with regard to the CNT content, the sonication time and the total sonication energy input. The CNT dispersion conditions were of key importance for both the thermo-mechanical and toughness properties of the modified systems. Sonication duration of 1 h was the most effective for the storage modulus and glass transition temperature (T_g) enhancement for both 0.5 and 1 wt.% CNT loadings. The significant increase of the storage modulus and T_g under specific sonication conditions was associated with the improved dispersion and interfacial bonding between the CNTs and the epoxy matrix. Sonication energy was the influencing parameter for the toughness properties. Best results were obtained for 2 h of sonication and 50% sonication amplitude. It was suggested that this level of sonication allowed appropriate dispersion of the CNTs to the epoxy matrices without destroying the CNT’s structure.     

Microstructure and properties of polyurethane nanocomposites reinforced with methylene-bis-ortho-chloroanilline-grafted multi-walled carbon nanotubes

Methylene-bis-ortho-chloroanilline (MOCA), an excellent cross-linker widely used to prepare cured polyurethane (PU) elastomers with high performance, was used to modify a multi-walled carbon nanotube. PU/carbon nanotube (CNT) nanocomposites were prepared by incorporation of the MOCA-grafted CNT into PU matrix. Fourier transform infrared spectra have shown that the modified CNTs have been linked with PU matrix. The microstructure of composites was investigated by Field-Emission Scanning Electron Microscopy. The results of Dynamic Mechanical Thermal Analysis and Differential Scanning Calorimetry have investigated the grafted CNTs as cross-linker in the cured composites. The studies on the thermal and mechanical properties of the composites have indicated that the storage modulus and tensile strength, as well as glass transition temperature and thermal stability are significantly increased with increasing CNT content.     

A comprehensive study on thermal conductivities of wavy carbon nanotube-reinforced cementitious nanocomposites

The thermal conductivities of cementitious nanocomposites reinforced by wavy carbon nanotubes (CNTs) are determined by the effective medium (EM) micromechanics-based method. The nanocomposite is composed of sinusoidally wavy CNTs as reinforcement and cement paste as matrix. The interfacial region between the CNTs and cementitious material is considered in the analysis. The effects of volume fraction and waviness parameters of CNTs, interfacial thermal resistance, type of CNTs placement within the matrix including aligned or randomly oriented CNTs, cement paste properties on the thermal conductivity coefficients of the nanocomposite are studied. The estimated values of the model are in very good agreement with available experimental data. Two parameters of CNT waviness and interfacial region contributions should be included in the modeling to predict realistic results for both aligned and randomly oriented CNT-reinforced nanocomposites. The results reveal that thermal conductivities K₂₂ (transverse in-plane thermal conductivity) and K₃₃ (longitudinal in-plane thermal conductivity) of the nanocomposites are remarkably dependent on the CNT waviness. Also, it is found that the CNT waviness moderately affects the thermal conductivity of a cementitious nanocomposite containing randomly oriented CNTs. However, the non-straight shape of CNTs does not influence the value of thermal conductivity K₁₁ (transverse out of plane thermal conductivity). The achieved results can be useful to guide the design of cementitious nanocomposites with optimal thermal conductivity properties.     

Effect of surfactant treatment on thermal stability and mechanical properties of CNT/polybenzoxazine nanocomposites

The mechanical and thermo-mechanical properties of polybenzoxazine nanocomposites containing multi-walled carbon nanotubes (MWCNTs) functionalized with surfactant are studied. The results are specifically compared with the corresponding properties of epoxy-based nanocomposites. The CNTs bring about significant improvements in flexural strength, flexural modulus, storage modulus and glass transition temperature, T_g, of CNT/polybenzoxazine nanocomposites at the expense of impact fracture toughness. The surfactant treatment has a beneficial effect on the improvement of these properties, except the impact toughness, through enhanced CNT dispersion and interfacial interaction. The former four properties are in general higher for the CNT/polybenzoxazine nanocomposites than the epoxy counterparts, and vice versa for the impact toughness. The addition of CNTs has an ameliorating effect of lowering the coefficient of thermal expansion (CTE) of polybenzoxazine nanocomposites in both the regions below and above T_g, whereas the reverse is true for the epoxy nanocomposites. This observation has a particular implication of exploiting the CNT/polybenzoxazine nanocomposites in applications requiring low shrinkage and accurate dimensional control.     

Mechanical,electrical and thermal properties of aligned carbon nanotube/polyimide composites

Carbon nanotubes (CNTs) have high strength and modulus, large aspect ratio, and good electrical and thermal conductivities, which make them attractive for fabricating composite. The poly(biphenyl dianhydride-p-phenylenediamine) (BPDA/PDA) polyimide has good mechanical and thermal performances and is herein used as matrix in unidirectional carbon nanotube composites for the first time. The strength and modulus of the composite increase by 2.73 and 12 times over pure BPDA–PDA polyimide, while its electrical conductivity reaches to 183 S/cm, which is 10¹⁸ times over pure polyimide. The composite has excellent high temperature resistance, and its thermal conductivity is beyond what has been achieved in previous studies. The improved properties of the composites are due to the long CNT length, high level of CNT alignment, high CNT volume fraction and good CNT dispersion in polyimide matrix. The composite is promising for applications that require high strength, lightweight, or high electrical and thermal conductivities.     

Isothermal crystallization behavior and mechanical properties of polylactide/carbon nanotube nanocomposites

Carbon nanotube (CNT)–reinforced polylactide (PLA) nanocomposites were prepared using a melt compounding process employing a twin-screw extruder. The isothermal crystallization kinetics of PLA/CNT nanocomposites according to Avrami’s theory were analyzed using differential scanning calorimetry in the temperature range 90–120 °C. There was a significant dependence of CNT on the crystallization behavior of the PLA matrix. The incorporation of CNT improved effectively the crystallization rate of PLA/CNT nanocomposites through heterogeneous nucleation. The nucleating effect of CNTs which increased the number of nucleation sites and decreased the average spherulite size was confirmed using polarized optical microscopy. The rheological properties of the PLA/CNT nanocomposites were also investigated. Changes in the microstructure of the PLA/CNT nanocomposites occurred by incorporating CNT. Furthermore, the tensile strength/modulus and thermal stability of PLA/CNT nanocomposites were enhanced when a very small quantity of CNT was added. This research accounts for the effect of CNTs, which significantly influenced the isothermal behavior, thermal stability, mechanical, and rheological properties of the PLA/CNT nanocomposites, providing a design guide for PLA/CNT nanocomposites in industrial fields.     

Effect of nanofiber on material properties of vapor-grown carbon nanofiber reinforced thermoplastic polyurethane (TPU/CNF) nanocomposites prepared by melt compounding

The present work deals with the preparation of the CNF based TPU nanocomposites by melt blending to explore the effect of state of dispersion and wt.% loading of CNF on material properties. In addition, the morphology, mechanical, thermal, rheological, and electrical properties of the nanocomposites have been evaluated through various characterization techniques with an aim to find the suitability of the nanocomposites for industrial applications. Transmission electron microscopy (TEM) study reveals that the CNFs exhibited a uniformly dispersed in TPU matrix. The thermal stability of the TPU evaluated by thermogravimetric analysis (TGA) showed significant increase with increased CNF content. It is observed that storage modulus (E′) and glass transition temperature (T_g) of the TPU matrix increases by the incorporation of CNF. The melting point (T_m) and the T_g of soft segments observed from the differential scanning calorimetry (DSC) were found to shift towards higher temperature with the inclusion of CNF.     

Enhanced thermal and mechanical properties of carbon nanotube composites through the use of functionalized CNT-reactive polymer linkages and three-roll milling

We report enhanced thermal and mechanical properties of carbon nanotube (CNT) composites achieved through the use of functionalized CNTs-reactive polymer linkages and three-roll milling. CNTs were functionalized with carboxyl groups and dispersed in a polymer containing an epoxide group resulting in a chemical reaction. To maximize CNT dispersion for practical usage, entangled CNTs are separated and then evenly dispersed within the polymer matrix using three horizontally positioned rotating rolls that apply a strong shear force to the composite. Consequently, accompanying with thermal stability, elastic modulus and storage modulus of such functionalized CNT/polymer composites were increased by 100% and 500% that of the untreated epoxy polymer.     

Influence of carbon nanotube-polymeric compatibilizer masterbatches on morphological, thermal, mechanical, and tribological properties of polyethylene

Study was made of the effect of multiwall carbon nanotubes (MWCNTs) and polymeric compatibilizer on thermal, mechanical, and tribological properties of high density polyethylene (HDPE). The composites were prepared by melt mixing in two steps. Carbon nanotubes (CNTs) were melt mixed with maleic anhydride grafted polyethylene (PEgMA) as polymeric compatibilizer to produce a PEgMA-CNT masterbatch containing 20 wt% of CNTs. The masterbatch was then added to HDPE to prepare HDPE nanocomposites with CNT content of 2 or 6 wt%. The unmodified and modified (hydroxyl or amine groups) CNTs had similar effects on the properties of HDPE-PEgMA indicating that only non-covalent interactions were achieved between CNTs and matrix. According to SEM studies, single nanotubes and CNT agglomerates (size up to 1 μm) were present in all nanocomposites regardless of content or modification of CNTs. Addition of CNTs to HDPE-PEgMA increased decomposition temperature, but only slight changes were observed in crystallization temperature, crystallinity, melting temperature, and coefficient of linear thermal expansion (CLTE). Young’s modulus and tensile strength of matrix clearly increased, while elongation at break decreased. Measured values of Young’s moduli of HDPE-PEgMA-CNT composites were between the values of Young’s moduli for longitudinal (E₁₁) and transverse (E₂₂) direction predicted by Mori-Tanaka and Halpin-Tsai composite theories. Addition of CNTs to HDPE-PEgMA did not change the tribological properties of the matrix. Because of its higher crystallinity, PEgMA possessed significantly different properties from HDPE matrix: better mechanical properties, lower friction and wear, and lower CLTE in normal direction. Interestingly, the mechanical and tribological properties and CLTEs of HDPE-PEgMA-CNT composites lie between those of PEgMA and HDPE.     

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.     

Interface tailoring to enhance mechanical properties of carbon nanotube reinforced magnesium composites

This study highlights the use of a metallic coating of nanoscale thickness on carbon nanotube to enhance the interfacial characteristics in carbon nanotube reinforced magnesium (Mg) composites. Comparisons between two reinforcements were targeted: (a) pristine carbon nanotubes (CNTs) and (b) nickel-coated carbon nanotubes (Ni–CNTs). It is demonstrated that clustering adversely affects the bonding of pristine CNTs with Mg particles. However, the presence of nickel coating on the CNT results in the formation of Mg₂Ni intermetallics at the interface which improved the adhesion between Mg/Ni–CNT particulates. The presence of grain size refinement and improved dispersion of the Ni–CNT reinforcements in the Mg matrix were also observed. These result in simultaneous enhancements of the micro-hardness, ultimate tensile strength and 0.2% yield strength by 41%, 39% and 64% respectively for the Mg/Ni–CNT composites in comparison with that of the monolithic Mg.     

Evaluation and modelling of electrically conductive polymer nanocomposites with carbon nanotube networks

Superior electrical, thermal, and mechanical properties of carbon nanotubes (CNTs) have made them effective filler for multifunctional polymer nanocomposites (PNCs). In particular, electrically conductive PNCs filled with CNTs have been researched extensively. These studies aimed to increase the PNCs' electrical conductivity (σ) and to minimize the percolation thresholds (ϕ_c). In this work, we have developed an improved model to describe the CNT networks and thereby evaluate the PNCs' ϕ_c and σ. The new model accounts for the electrical conductance contributed by the continued CNT network across the boundary of adjacent representative volume elements. It more realistically represents the interconnectivity among CNTs and enhances the evaluation of the structure-to-property relationship of PNCs' σ.     

Synthesis and properties of poly(hexamethylene terephthalate)/multiwall carbon nanotubes nanocomposites

Poly(hexamethylene terephthalate) (PHT)/carbon nanotubes (CNT) nanocomposites containing 1% and 3% (w/w) of filler were prepared by two procedures: in situ ring-opening polymerization of hexamethylene terephthalate cyclic oligomers in the presence of CNT and melt blending of PHT/CNT mixtures. Arc discharge multiwalled carbon nanotubes, both pristine (MWCNT) and hydroxyl functionalized (MWCNT-OH), were used. The objective was to evaluate the effect of preparation procedure, nanotube side-wall functionalization and amount of nanotube loaded on properties of PHT. All nanocomposites showed an efficient distribution of the carbon nanotubes within the PHT matrix but interfacial adhesion and reinforcement effect was dependent on both functionalization and nanotubes loading. Significant differences in thermal stability and mechanical properties ascribable to functionalization and processing were observed among the prepared nanocomposites. All the prepared nanocomposites showed enhanced crystallizability due to CNT nucleating effects although changes in melting and glass transition temperatures were not significant.     

Effects of carbon black-carbon nanotube complex fillers on the properties of isotactic polypropylene nanocomposites

In this study, the reinforcing effects of carbon black (CB) and carbon nanotube (CNT) complex fillers on the properties of isotactic polypropylene (iPP) nanocomposites were investigated using various methods. The surface of the CNTs was modified using a linear alkyl chain in order to create a homogeneous CNT dispersion in the iPP matrix. When the CB content that was incorporated in the iPP matrix increased, the thermal and mechanical properties of the iPP/CB nanocomposites were enhanced. Additionally these enhancements in the properties were similarly induced by introducing a small amount of alkylated CNTs (a-CNTs). In contrast, the CB/a-CNT complex filler was more effective for the iPP nanocomposites than the CB or a-CNT single filler in terms of the thermal stability and the electrical properties. However, the mechanical properties of the CB/a-CNT complex filler incorporated iPP nanocomposites were poorer than the only a-CNT incorporated iPP nanocomposites. Additionally, the complex filler did not overcome the nucleation behavior of the a-CNTs in the re-crystallization of iPP.     

A study on the tensile response and fracture in carbon nanotube-based composites using molecular mechanics

A study on the mechanical properties of polyethylene and carbon nanotube (CNT) based composites is presented using molecular mechanics simulations. The systems being investigated consist of amorphous as well as crystalline polyethylene (PE) composites with embedded single-walled CNTs. All the systems are subjected to quasi-static tensile loading, with the assumption that no cross-link chemical bonds exist between the CNT and polyethylene matrix in the case of nanocomposites. Based on the numerical simulations, we report Young’s moduli (C₃₃) of 212–215 GPa for crystalline PE, which closely match the experimental measurement. Furthermore, elastic stiffness of 3.19–3.69 GPa and tensile strength of 0.21–0.25 GPa are obtained for amorphous PE. The tensile responses are found to be highly isotropic. In the case of crystalline PE reinforced by long through CNTs, moderate improvements in the tensile strength and elastic stiffness are observed. However, the results differ from the predictions using the rule of mixtures. On the other hand, although significant increase in the overall tensile properties is observed when amorphous PE is reinforced by long through CNTs, the load transfer at the nanotube/polymer interface has negligible effect. Finally, degradations in both tensile strength and elastic stiffness are reported when amorphous PE is reinforced by embedded CNTs. The study presented indicates the importance of specific CNT and polymer configurations on the overall properties of the nanocomposite.     

Simulated strength and structure of carbon–carbon reinforced composite

The atomistic simulations of carbon nanotube (CNT) – carbon reinforced composite material are reported. The studied composite samples are obtained by impregnating certain amounts of CNTs (3,3) and (6,6) into a pristine graphite matrix. The addition of CNTs is found to be of significant usefulness for the CNT–reinforced composites, since it allows to achieve extreme lightness and strength. Being impregnated into graphite matrix, CNTs are able to increase the critical component of its initially highly anisotropic Young modulus by 2–8 times. The linear thermal expansion coefficients do not exceed 10⁻⁶ to 10⁻⁵ K⁻¹, making this material applicable for novel aviation and space vehicles. The degree of dispersion of CNTs within graphite matrix is found to drastically influence composite properties.     

Self-sensing and mechanical performance of CNT/GNP/UHMWPE biocompatible nanocomposites

Ultra-high molecular weight polyethylene (UHMWPE)-based conductive nanocomposites with reduced percolation and tunable piezoresistive behavior were prepared via solution mixing followed by compression molding using carbon nanotubes (CNT) and graphene nanoplatelets (GNP). The effect of varying wt% of GNP with fixed CNT content (0.1 wt%) on the mechanical, electrical, thermal and piezoresistive properties of UHMWPE nanocomposites was evaluated. The combination of CNT and GNP enhanced the dispersion in UHMWPE matrix and lowered the probability of CNT aggregation as GNP acted as a spacer to separate the entanglement of CNT with each other. This has allowed the formation of an effective conductive path between GNP and CNT in UHMWPE matrix. The thermal conductivity, degree of crystallinity and degradation temperature of the nanocomposites increased with increasing GNP content. The elastic modulus and yield strength of the nanocomposites were improved by 37% and 33%, respectively, for 0.1/0.3 wt% of CNT/GNP compared to neat UHMWPE. The electrical conductivity was measured using four-probe method, and the lowest electrical percolation threshold was achieved at 0.1/0.1 wt% of CNT/GNP forming a nearly two-dimensional conductive network (critical value, t = 1.20). Such improvements in mechanical and electrical properties are attributed to the synergistic effect of the two-dimensional GNP and one-dimensional CNT which limits aggregation of CNTs enabling a more efficient conductive network at low wt% of fillers. These hybrid nanocomposites exhibited strong piezoresistive response with sensitivity factor of 6.2, 15.93 and 557.44 in the linear elastic, inelastic I and inelastic II regimes, respectively, for 0.1/0.5 wt% of CNT/GNP. This study demonstrates the fabrication method and the self-sensing performance of CNT/GNP/UHMWPE nanocomposites with improved properties useful for orthopedic implants.     

Reinforcement of SC-15 epoxy with CNT/CNF under high magnetic field: an investigation of mechanical and thermal response

We report here reinforcement of SC-15 epoxy matrix with 1.0 wt% loading of carbon nanotubes (CNTs)/carbon nanofibers (CNFs), and cured under a high (28 T) magnetic field. The improvement in mechanical properties such as compressive strength and stiffness was phenomenal with CNT inclusion, about 126% and 166% increase in strength and modulus, respectively. Enhancement in the glass transition (T _g) and thermal decomposition temperatures was also significant, by about 30 and 23 °C, respectively. Although the degree of anisotropy introduced by the magnetic field was not significant, it was observed that almost half of the improvement was due to magnetic flocculation. In the following is described the results of initial experiments conducted in the National High Magnetic Field Laboratory (NHMFL). Enhanced properties of the nanocomposites strongly suggest improved ordering of nanoparticles within the matrix.     

Characterization of IrO2/CNT nanocomposites

IrO₂ nanocrystals (NCs) were grown on vertically aligned carbon nanotube (CNT) templates, forming IrO₂/CNT nanocomposites, by metal organic chemical vapour deposition using (C₆H₇)(C₈H₁₂)Ir as a source reagent. The surface morphology, structural and spectroscopic properties of the nanocomposites were characterized using field-emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and Raman scattering. IrO₂ varied from particle- to tube-like NCs as the deposition time increased from 5 to 60 min. The particle-like IrO₂ NCs may be used as a protective layer on CNTs, providing stable and uniform field emission application. The tube-like structure may increase the surface-to-volume ratio which makes the IrO₂/CNT nanocomposites as an attractive candidate for the supercapacitor application.     

Fabrication of microwave exfoliated graphite oxide reinforced thermoplastic polyurethane nanocomposites: Effects of filler on morphology,mechanical, thermal and conductive properties

Different formulations of microwave-exfoliated graphite oxide (MEGO) based thermoplastic polyurethane (TPU) nanocomposites were successfully prepared via melt blending followed by injection molding. The spectroscopic study indicated that a strong interfacial interaction had developed between the MEGO and the TPU matrix. The microscopic observations showed that the MEGO layers were homogeneously dispersed throughout the TPU matrix. Thermal analysis indicated that the glass transition temperatures (T_g) of the nanocomposites increased with increasing MEGO content and their thermal stability improved in comparison with pure TPU matrix. The mechanical properties of nanocomposites improved substantially by the incorporation of MEGO into the TPU matrix. Electrical conductivity test indicated that a conductivity of 10⁻⁴ S cm⁻¹ was achieved in the nanocomposite containing only 4.0 wt.% of MEGO.