Strain sensing in polymer/carbon nanotube composites by electrical resistance measurement

In this work multiwall carbon nanotubes (MWCNTs) dispersed in a polymer matrix have been used for strain sensing of the resulting nanocomposite under tensile loading. This was achieved by measuring the relative electrical resistance change (ΔR/R₀) in conductive polyvinylidenefluoride (PVDF)/MWCNTs nanocomposites prepared by melt-mixing with varying filler content from 0.5 wt.% to 8 wt.%. Two main parameters were systematically studied. The PVDF/MWCNTs mixing procedure that results in a successful MWCNTs dispersion, and the effect of MWCNTs content on material’s sensing behaviour. The samples were subjected to tensile loading and the longitudinal strain was monitored together with the longitudinal electrical resistance. The results showed that MWCNTs dispersed in insulating PVDF matrix have the potential to be used as a sensitive network to monitor the strain levels in polymer/carbon nanotube nanocomposites as the deformation level of each sample was being reflected by the resistance changes.     

Molecular dynamics simulations of orientation induced interfacial enhancement between single walled carbon nanotube and aromatic polymers chains

In this work, molecular dynamics simulations were utilized to probe the interfacial enhancement between aromatic polymers and single walled carbon nanotube (SWCNT) induced by molecular orientation. Two aromatic polymers, polyphenylene sulfide (PPS) and polystyrene (PS) were chosen for comparison study. It was found that orientation of polymer chain could bring about an obvious promotion in interfacial interaction for both systems. In PPS/SWCNT systems, the increased interfacial interaction energy was due to the easy formation of offset π–π stacking, while in PS/SWCNT systems the formation of edge-to-face π–π stacking contributed to the enhancement. Polymer/SWCNT composites were also constructed and a similar interfacial enhancement was observed as well. The mechanism of the orientation induced enhancement was a combination of forming more π–π stacking and better coating effect. This will help to deepen the understanding of interfacial interaction in aromatic polymers/carbon nanotubes composites and guide the fabrication of high performance materials.     

Enhanced dielectric and ferroelectric properties induced by TiO2@MWCNTs nanoparticles in flexible poly(vinylidene fluoride) composites

Flexible polymer based composites containing multi-walled carbon nanotubes (MWCNTs) have been reported to present high dielectric constant. However, the composites generally exhibit high dielectric loss and low dielectric breakdown strength, which prohibits their practical use in electronic and electric industry. MWCNTs were coated with a continuous layer of TiO₂ nanoparticles (TiO₂@MWCNTs) by a simple hydrothermal process and TiO₂@MWCNTs/poly(vinylidene fluoride) (PVDF) composites were prepared by a solution casting method. Compared to the pristine MWCNTs/PVDF composites, the TiO₂@MWCNTs/PVDF composites presented enhanced dielectric constant and lower dielectric loss. Additionally, the breakdown strength of the TiO₂@MWCNTs/PVDF composites was also improved, which is favorable for enhanced ferroelectric properties in the composites.     

Crystallization,mechanical performance and hydrolytic degradation of poly(butylene succinate)/graphene oxide nanocomposites obtained via in situ polymerization

Poly(butylene succinate) (PBS)/graphene oxide (GO) nanocomposites were fabricated via in situ polymerization with very low GO content (from 0.03 to 0.5 wt%). The microstructures of the nanocomposites were characterized with Raman spectroscopy, fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), sedimentation experiments and atomic force microscopy (AFM). The results showed that PBS chains have been successfully grafted onto GO sheets during in-situ polymerization, accompanied by the thermo-reduction from GO to graphene. The grafted GO displayed a great nucleating effect on PBS crystallization, resulting in largely improved crystallization temperature and decreased spherules size. A simultaneous enhancement in tensile strength and elongation was achieved for PBS/GO nanocomposites fiber. Meanwhile, increase in hydrolytic degradation rate was also observed for these nanohybrids. Our result indicates that using very low content GO is a simple way to achieve good dispersion yet with remarkable property enhancement for polymer/GO nanocomposites.     

Preparation of continuous carbon nanotube networks in carbon fiber/epoxy composite

In order to optimize carbon nanotube (CNT) dispersion state in fiber/epoxy composite, a novel kind of CNT organization form of continuous networks was designed. The present work mainly discussed the feasibility of preparing continuous CNT networks in composite: Fiber fabric was immersed into CNT aqueous solution (containing dispersant) followed by freeze drying and pyrolysis process, prior to epoxy infusion. The morphologies of fabric with CNTs were observed by Scanning Electron Microscope. The relationship between CNT networks and flowing epoxy resin was studied. Properties of composite, including out-of-plane electrical conductivity and interlaminar shear strength (ILSS), were measured. The results demonstrated that continuous and porous CNT networks formed by entangled CNTs could be assembled in fiber fabric. Most part of them were preserved in composite due to the robustness of network structures. The preserved CNT networks significantly improved out-of-plane electrical conductivity, and also have an effect on ILSS value.     

Electrical properties of polyvinylidene fluoride (PVDF)/multi-walled carbon nanotube (MWCNT) semi-transparent composites: Modelling of DC conductivity

Transparent conductive composites can be achieved from PVDF–MWCNT at very low concentration of MWCNT. These composites show different degree of UV–Visible radiation absorption depending on MWCNT concentration in composites. The composition dependent dielectric properties and AC conductivity were also measured for these composites. Properties like AC conductivity, dielectric constant and loss are increasing with filler concentration. The variations of DC conductivity against composition and temperature are also reported. The electrical hysteresis and electrical set are observed for PVDF–MWCNT composites when subjected to heating–cooling cycle. The validity of different theoretical models depicting percolation threshold with respect to DC conductivity was tested for these composites.     

The influence of nano/micro hybrid structure on the mechanical and self-sensing properties of carbon nanotube-microparticle reinforced epoxy matrix composite

Nano/micrometer hybrids are prepared by chemical vapor deposition growth of carbon nanotubes (CNTs) on SiC, Al₂O₃ and graphene nanoplatelet (GNP). The mechanical and self-sensing behaviors of the hybrids reinforced epoxy composites are found to be highly dependent on CNT aspect ratio (AR), organization and substrates. The CNT–GNP hybrids exhibit the most significant reinforcing effectiveness, among the three hybrids with AR1200. During tensile loading, the in situ electrical resistance of the CNT–GNP/epoxy and the CNT–SiC/epoxy composites gradually increases to a maximum value and then decreases, which is remarkably different from the monotonic increase in the CNT–Al₂O₃/epoxy composites. However, the CNT–Al₂O₃ with increased AR ⩾ 2000 endows the similar resistance change as the other two hybrids. Besides, when AR < 3200, the tensile modulus and strength of the CNT–Al₂O₃/epoxy composites gradually increase with AR. The interrelationship between the hybrid structure and the mechanical and self-sensing behaviors of the composites are analyzed.     

Study on thermal properties of graphene foam/graphene sheets filled polymer composites

The polymer composites composed of graphene foam (GF), graphene sheets (GSs) and pliable polydimethylsiloxane (PDMS) were fabricated and their thermal properties were investigated. Due to the unique interconnected structure of GF, the thermal conductivity of GF/PDMS composite reaches 0.56 W m⁻¹ K⁻¹, which is about 300% that of pure PDMS, and 20% higher than that of GS/PDMS composite with the same graphene loading of 0.7 wt%. Its coefficient of thermal expansion is (80–137) × 10⁻⁶/K within 25–150 °C, much lower than those of GS/PDMS composite and pure PDMS. In addition, it also shows superior thermal and dimensional stability. All above results demonstrate that the GF/PDMS composite is a good candidate for thermal interface materials, which could be applied in the thermal management of electronic devices, etc.     

A comparative study of the load transfer mechanisms of the carbon nanotube reinforced polymer composites with interfacial crystallization

With the help of shear-lag theory, load transfer analysis is performed on the carbon nanotube reinforced polymer composites with interfacial crystallization of different morphologies, including transcrystallinity layer (TCL) and nanohybrid shish-kebab (NHSK) structures. By comparison, we find that the TCL structures can ease the burden of the CNT while the NHSK structures can lead to a fluctuating distribution of the axial stress in the CNT. Both structures can improve the effective elastic modulus of the composites, though the effect of the TCL structures is more pronounced. Besides, the enhancement of the load transfer efficiency of the composites is also observed, the study of the interfacial stress on different kinds of interfaces shows that the reinforcing effect of the TCL structures is sensitive to both the CNT/crystalline polymer interface and crystalline polymer/amorphous polymer interface, while the major decisive factor for the NHSK structures is confined to be the CNT/crystalline polymer interface because of the interlocking effect. Based on these features, some suggestions are given for tailoring the high-performance carbon nanotube reinforced polymer composites.     

Significantly improving infrared light-induced shape recovery behavior of shape memory polymeric nanocomposite via a synergistic effect of carbon nanotube and boron nitride

The present work studies the thermomechanical properties and infrared light-induced shape memory effect (SME) in shape memory polymer (SMP) nanocomposite incorporated with carbon nanotube (CNT) and boron nitride. The combination of CNT and boron nitride results in higher glass transition temperature, mechanical strength and thermomechanical strength. While CNTs are employed to improve the absorption of infrared light and thermally conductive property of SMP, boron nitrides facilitate heat transfer from CNTs to the polymer matrix and thus to enable fast response. A unique synergistic effect of CNT and boron nitride was explored to facilitate the heat transfer and accelerate the infrared light-induced shape recovery behavior of the shape memory polymeric nanocomposite.     

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.     

Dynamic fracture of carbon nanotube/epoxy composites under high strain-rate loading

We investigate dynamic fracture of three types of multiwalled carbon nanotube (MWCNT)/epoxy composites and neat epoxy under high strain-rate loading (${10}^5''–''{10}^6$ s⁻¹). The composites include randomly dispersed, 1 wt%, functionalized and pristine CNT/epoxy composites, as well as laminated, ∼50 wt% CNT buckypaper/epoxy composites. The pristine and functionalized CNT composites demonstrate spall strength and fracture toughness slightly higher and lower than that of neat epoxy, respectively, and the spall strength of laminated CNT buckypaper/epoxy composites is considerably lower; both types of CNTs reduce the extent of damage. Pullout, sliding and immediate fracture modes are observed; the fracture mechanisms depend on the CNT–epoxy interface strength and fiber strength, and other microstructures such as the interface between CNT laminates. Compared to the functionalized CNT composites, weaker CNT–epoxy interface strength and higher fiber strength lead to a higher probability of sliding fracture and higher tensile strength in the pristine CNT composites at high strain rates. On the contrary, sliding fracture is more pronounced in the functionalized CNT composites under quasistatic loading, a manifestation of a loading-rate effect on fracture modes. Despite their helpful sliding fracture mode and large CNT content, the weak laminate–laminate interfaces play a detrimental role in fracture of the laminated CNT buckypaper/epoxy composites. Regardless of materials, increasing strain rates leads to pronounced rise in tensile strength and fracture toughness.     

Combined effects of fiber/matrix interface and water absorption on the tribological behaviors of water-lubricated polytetrafluoroethylene-based composites reinforced with carbon and basalt fibers

Tribological behaviors of two PTFE-based composites reinforced with carbon fibers and basalt fibers sliding against stainless steel under water lubrication were investigated and compared with those of pure PTFE. Results showed that carbon fibers were well bonded with PTFE matrix by dendritic PTFE nano-ribbons in a Boston ivy-like manner, but the basalt fibers were poorly bonded with the matrix. Due to the great accelerating effect of poor fiber/matrix interfacial adhesion on water absorption, BF/PTFE with the highest crystallinity unexpectedly showed the highest water absorption, resulting in serious matrix plasticization and degradation of fiber/matrix interfacial adhesion. As a result, as the reinforcement failure of basalt fibers occurred, BF/PTFE exhibited the highest wear rate. Instead, because good fiber/matrix interfacial adhesion was favor of the resistance to water intrusion, CF/PTFE composite was not dominated by remarkable matrix plasticization and fiber/matrix interface degradation, and showed the lowest wear rate.     

Toughness,flexural, damping and interfacial properties of hybridized GFRE composites with MWCNTs

As the improved damping in fiber-reinforced composites can affect the other mechanical properties, therefore, the aim of this work is to investigate the effect of multiwall carbon nanotube (MWCNT) on the interfacial bond strength, flexural strength and stiffness, toughness and damping properties of hybridized glass-fiber reinforced epoxy (GFRE) composites. Nanophased epoxy resin was used to hybridize unidirectional and quasi-isotropic GFRE composites with [0/±45/90]_s and [90/±45/0]_s stacking sequences. Results from the interfacial characterizations of the hybridized composites showed improvement up to 30% compared to the control laminates. Hybridization of GFRE laminates with MWCNTs leads to decreasing the flexural and storage moduli, increasing flexural strength, toughness, natural frequencies and damping ratio. A high correlation coefficient of 0.9985 was obtained between static flexural and dynamic storage moduli. The highest flexural strength, flexural and storage moduli and natural frequency of quasi-isotropic laminate were observed for [0/±45/90]_s stacking sequence and vice versa for damping ratio.     

Combination effect of carbon nanotubes with graphene on intumescent flame-retardant polypropylene nanocomposites

A novel polypropylene (PP) nanocomposite was fabricated by the incorporation of intumescent flame retardant (IFR), carbon nanotubes (CNTs) and graphene into the PP matrix. Results from TEM indicate that IFR, CNTs and exfoliated graphene nanosheets are dispersed finely in the PP matrix, which is supported by the XRD analysis results. Thermogravimetric (TGA) results show that the addition of IFR, CNTs and graphene improved the thermal stability and the char yields of PP. The PP/IFR/CNTs/RGO nanocomposites, filled with 18 wt% IFR, 1 wt% CNTs and 1 wt% graphene, achieve the limiting oxygen index value of 31.4% and UL-94 V0 grade. Cone calorimeter data reveal that combustion behavior, heat release rate peak (PHRR) and average specific extinction area (ASEA) of PP decrease substantially when combination effects of IFR, CNTs and graphene intervene. For the PP/IFR/CNTs/RGO nanocomposites, the PHRR exhibits an 83% reduction and the time of ignition is delayed 40 s compared with neat PP.     

Nano-epoxy resins containing electrospun carbon nanofibers and the resulting hybrid multi-scale composites

For the first time, electrospun carbon nanofibers (ECNFs, with diameters and lengths of ∼200 nm and ∼15 μm, respectively) were explored for the preparation of nano-epoxy resins; and the prepared resins were further investigated for the fabrication of hybrid multi-scale composites with woven fabrics of conventional carbon fibers via the technique of vacuum assisted resin transfer molding (VARTM). For comparison, vapor growth carbon nanofibers (VGCNFs) and graphite carbon nanofibers (GCNFs) were also studied for making nano-epoxy resins and hybrid multi-scale composites. Unlike VGCNFs and GCNFs that are prepared by bottom-up methods, ECNFs are produced through a top-down approach; hence, ECNFs are more cost-effective than VGCNFs and GCNFs. The results indicated that the incorporation of a small mass fraction (e.g., 0.1% and 0.3%) of ECNFs into epoxy resin would result in substantial improvements on impact absorption energy, inter-laminar shear strength, and flexural properties for both nano-epoxy resins and hybrid multi-scale composites. In general, the reinforcement effect of ECNFs was similar to that of VGCNFs, while it was higher than that of GCNFs.     

Facile preparation of graphene nanoribbon filled silicone rubber nanocomposite with improved thermal and mechanical properties

In the present study, graphene nanoribbon was prepared through unzipping the multi walled carbon nanotubes, and its reinforcing effect as a filler to the silicone rubber was further investigated. The results showed that carbon nanotubes could be unzipped to graphene nanoribbon using strong oxidants like potassium permanganate and sulfuric acid. The prepared graphene nanoribbon could homogeneously disperse within silicone rubber matrix using a simple solution mixing approach. It was also found from the thermogravimetric analysis curves that the thermal stability of the graphene nanoribbon filled silicone rubber nanocomposites improved compared to the pristine silicone rubber. Besides, with the incorporation of the nanofiller, the mechanical properties of the resulting nanocomposites were significantly enhanced, in which both the tensile stress and Young’s modulus increased by 67% and 93% respectively when the mass content of the graphene nanoribbon was 2.0 wt%. Thus it could be expected that graphene nanoribbon had large potentials to be applied as the reinforcing filler to fabricate polymers with increased the thermal and mechanical properties.     

Waterproof characteristics of nanoclay/epoxy nanocomposite in adhesively bonded joints

When adhesively bonded joints are exposed to a moist environment, the tensile load capability of the joint is significantly decreased because moisture absorption weakens the mechanical properties of epoxy adhesive. In this paper, a nanoclay with excellent penetration resistance properties was used as a filler in epoxy adhesive in order to enhance adhesive strength in moist environments. The water absorption of the epoxy adhesive and the adhesive strength of the adhesively bonded joints were measured in water absorption experiments with respect to the weight fraction of the nanoclay and the moisture exposure time. These results showed that the tensile load capability of the nanoclay-filled adhesively bonded joint was greatly enhanced, even in a moist environment, because the nanoclay reduced water absorption into the epoxy adhesive as well as into the interface between the epoxy adhesive and the steel adherend and increased the strength of the epoxy adhesive itself.     

Effect of silica coating thickness on the thermal conductivity of polyurethane/SiO2 coated multiwalled carbon nanotube composites

Silica coated multiwalled carbon nanotubes (SiO₂@MWCNTs) with different coating thicknesses of ∼4 nm, 30–50 nm, and 70–90 nm were synthesized by a sol–gel method and compounded with polyurethane (PU). The effects of SiO₂@MWCNTs on the electrical properties and thermal conductivity of the resulting PU/SiO₂@MWCNT composites were investigated. The SiO₂ coating maintained the high electrical resistivity of pure PU. Meanwhile, incorporating 0.5, 0.75 and 1.0 wt% SiO₂@MWCNT (70–90 nm) into PU, produced thermal conductivity values of 0.287, 0.289 and 0.310 W/mK, respectively, representing increases of 62.1%, 63.3% and 75.1%. The thermal conductivity of PU/SiO₂@MWCNT composites was also increased by increasing the thickness of the SiO₂ coating.     

The filler–rubber interface and reinforcement in styrene butadiene rubber composites with graphene/silica hybrids: A quantitative correlation with the constrained region

Silica/reduced graphene oxide (SiO₂@rGO) hybrids were fabricated by an electrostatic assembly, and subsequently, SiO₂@rGO was incorporated into styrene butadiene rubber (SBR) to fabricate SBR composites. The dispersion status of SiO₂@rGO and the filler–rubber interfacial interaction were investigated. Likewise, the amount of constrained region was quantified and the findings suggested that the greater the volume fraction of constrained region has possessed, the stronger the interfacial interaction has had. Moreover, the contribution of constrained region to the performance of composites was quantitatively analyzed by the mechanical analysis and the tube model, and the results showed that it is the effect of constrained region, rather than the contents of SiO₂@rGO, which controls the reinforcement of composites. Specifically, the higher the volume fraction of constrained region is, the better the mechanical properties of composites will be. Also, SiO₂@rGO can be utilized as novel reinforcing filler for fabricating the green tire materials with high performance.