In this paper, an analytical model is developed for electrical conductivity of nanocomposites, particularly polymer/carbon nanotubes nanocomposites. This model considers the effects of aspect ratio, concentration, waviness, conductivity and percolation threshold of nanoparticles, interphase thickness, wettability between polymer and filler, tunneling distance between nanoparticles and network fraction on the conductivity. The developed model is confirmed by experimental results and parametric studies. The calculations show good agreement with the experimental data of different samples. The concentration and aspect ratio of nanoparticles directly control the conductivity. Moreover, a smaller distance between nanoparticles increases the conductivity based on the tunneling mechanism. A thick interphase also causes an increased conductivity, because the interphase regions participate in the networks and enhance the effectiveness of nanoparticles.

Cross model correlates the dynamic complex viscosity of polymer systems to zero complex viscosity, relaxation time and power-law index. However, this model disregards the growth of complex viscosity in nanocomposites containing filler networks, especially at low frequencies. The current paper develops the Cross model for complex viscosity of nanocomposites by yield stress as a function of the strength and density of networks. The predictions of the developed model are compared to the experimental results of fabricated samples containing poly(lactic acid), poly(ethylene oxide) and carbon nanotubes. The model’s parameters are calculated for the prepared samples, and their variations are explained. Additionally, the significances of all parameters on the complex viscosity are justified to approve the developed model. The developed model successfully estimates the complex viscosity, and the model’s parameters reasonably change for the samples. The stress at transition region between Newtonian and power-law behavior and the power-law index directly affects the complex viscosity. Moreover, the strength and density of networks positively control the yield stress and the complex viscosity of nanocomposites. The developed model can help to optimize the parameters controlling the complex viscosity in polymer nanocomposites.

Graphene was grown on molybdenum (Mo) foil by a chemical vapor deposition method at different growth temperatures (1000°C, 1100°C, and 1200°C). The properties of graphene were investigated by X-ray diffraction (XRD), X-ray photoelectron spectroscopy, and Raman spectroscopy. The results showed that the quality of the deposited graphene layer was affected by the growth temperature. XRD results showed the presence of a carbide phase on the Mo surface; the presence of carbide was more intense at 1200°C. Additionally, a higher I2D/IG ratio (0.418) was observed at 1200°C, which implies that there are fewer graphene layers at this temperature. The lowest ID/IG ratio (0.908) for the graphene layers was obtained at 1200°C, suggesting that graphene had fewer defects at this temperature. The size of the graphene domains was also calculated. We found that by increasing the growth temperature, the graphene domain size also increased.

Electrochemical synthesis was employed to prepare a novel hydroxyapatite/graphene (HAP/ Gr) composite powder suitable for medical applications as a hard tissue implant (scaffold). The synthesis was performed in a homogeneous dispersion containing Na2H2EDTA·2H2O, NaH2PO4 and CaCl2 with a Ca/EDTA/PO4 3− concentration ratio of 0.25/0.25/0.15M, along with 0.01 wt% added graphene nanosheets, at a current density of 137 mA cm−2 and pH value of 9.0. The field emission scanning electron microscopy and transmission electron microscopy observations of the composite HAP/Gr powder indicated that nanosized hydroxyapatite particles were uniformly placed in the graphene overlay. Raman spectroscopy, Fourier transform infrared spectroscopy and X-ray diffraction confirmed graphene incorporation in the HAP/Gr powder. The electrochemically prepared HAP/Gr composite powder exhibited slight antibacterial effect against the growth of the bacterial strain Staphylococcus aureus.

In recent years, flame synthesis has absorbed a great deal of attention as a combustion method for the production of metal oxide nanoparticles, carbon nanotubes, and other related carbon nanostructures, over the existing conventional methods. Flame synthesis is an energyefficient, scalable, cost-effective, rapid and continuous process, where flame provides the necessary chemical species for the nucleation of carbon structures (feed stock or precursor) and the energy for the production of carbon nanostructures. The production yield can be optimized by altering various parameters such as fuel profile, equivalence ratio, catalyst chemistry and structure, burner configuration and residence time. In the present report, diffusion and premixed flame synthesis methods are reviewed to develop a better understanding of factors affecting the morphology, positioning, purity, uniformity and scalability for the development of carbon nanotubes along with their correlated carbonaceous derivative nanostructures..

It has been demonstrated in a previous study that carbon nanotube (CNT)/epoxy/basalt composites produce better flexural properties than epoxy/basalt composites. In this study, mode I fracture tests were conducted using CNT/epoxy/basalt composites with and without seawater absorption in order to investigate the effect of the seawater absorption on the mode I fracture toughness (GIC) of the CNT/epoxy/basalt composites. The results demonstrated that the compliance of the seawater-absorbed specimen was larger than that of the dry specimen at the same crack length, while the opposite result was obtained for the fracture load. The GIC value of the seawater-absorbed CNT/epoxy/basalt composites was approximately 20% lower than that of the dry CNT/epoxy/basalt composites.