Highly oriented UHMWPE films were reinforced with functionalized graphene nanoplates (GNP). GNP was functionalized by deposition of polyaniline (PANI) on the GNP surface. The structure of GNP/PANI was studied by Raman spectroscopy, and the structure of xerogels and films based on UHMWPE was studied by DSC and SEM. PANI promotes the reduction of the GNP aggregation in the UHMWPE matrix and increases the degree of crystallinity due to heterogeneous crystallization. The new lamellar crystal structure has a high drawability. The highest value of the tensile strength 1330 MPa (an increase of 45%) was obtained with a filler content of 2 wt % GNP/PANI, and the highest value of Young’s modulus 41 GPa (an increase of 32%) was obtained with a filler content of 1 wt % GNP/PANI. The effect of GNP with PANI fillers on the dynamic mechanical properties of the UHMWPE films was discussed.

The paper considers the development of fillers representing mixtures of carbon nanotubes and graphene materials (graphene oxide and graphene nanoplatelets) in different mass ratios to modify epoxy resin. The graphene type and content effect on the dispersed phase particle effective sizes—both in aqueous suspensions and the resin—was analyzed. Hybrid particles were characterized by Raman spectroscopy and electron microscopy. The composites containing 0.15–1.00 wt.% CNTs/GO and CNTs/GNPs were thermogravimetrically analyzed, and their mechanical characteristics were determined. SEM images of the composite fracture surfaces were acquired. Optimal dispersions containing 75–100 nm particles were obtained at the CNTs:GO mass ratio of 1:4. It was shown that the CNTs can be located between the GO layers and on the GNP surface. The samples containing up to 0.2 wt.% CNTs/GO (at 1:1 and 1:4 ratios) were stable when heated in air up to 300 °C. For 0.15–0.20 wt.% CNTs/GO (at 1:1 ratio), the tensile strength and modulus of the composite increased by 84–88 and 40%, respectively. The increase in the strength characteristics was found to occur due to the interaction of the filler layered structure with the polymer matrix. The obtained composites can be used as structural materials in different fields of engineering.

A novel polyaniline-modified CNT and graphene-based nanocomposite (2.32–7.34 nm) was prepared and characterized by spectroscopic methods. The specific surface area was 176 m²/g with 0.232 cm³/g as the specific pore volume. The nanocomposite was used to remove zinc and lead metal ions from water; showing a high removal capacity of 346 and 581 mg/g at pH 6.5. The data followed pseudo-second-order, intraparticle diffusion and Elovich models. Besides this, the experimental values obeyed Langmuir and Temkin isotherms. The results confirmed that the removal of lead and zinc ions occurred in a mixed mode, that is, diffusion absorption and ion exchange between the heterogeneous surface of the sorbent containing active adsorption centers and the solution containing metal ions. The enthalpy values were 149.9 and 158.6 J.mol⁻¹K⁻¹ for zinc and lead metal ions. The negative values of free energies were in the range of −4.97 to −26.3 kJ/mol. These values indicated an endothermic spontaneous removal of metal ions from water. The reported method is useful to remove the zinc and lead metal ions in any water body due to the high removal capacity of nanocomposite at natural pH of 6.5. Moreover, a low dose of 0.005 g per 30 mL made this method economical. Furthermore, a low contact time of 15 min made this method applicable to the removal of the reported metal ions from water in a short time. Briefly, the reported method is highly economical, nature-friendly and fast and can be used to remove the reported metal ions from any water resource.