Abstract Prolonged exposure to environmental conditions such as ultraviolet radiation, humidity, and temperature, to which carbon fiber-reinforced thermoplastic polymer components are exposed during their service life, can lead to significant changes in mechanical, physical, and chemicals properties, and can often be irreversible, resulting in premature component failure. This study presents the influence of accelerated weathering exposure times (400 h, 800 h, and 1200 h) on the mechanical, thermal, and structural properties of carbon fiber (CF)/polyamide 6 (PA6) laminates. Analyses of composite surfaces were carried out using microscopy and contact angle measurements, which indicated that the factors of exposure to accelerated only affected the surface of the composites, showing signs of the beginning of degradation. The tensile strength (609 MPa ± 10 MPa) and interlaminar shear strength (27 MPa ± 0.9 MPa) did not present significant changes, showing that the reinforcement, the matrix, and the interface remained stable after exposure to accelerated.

Abstract Polyamide (PA) is a well-known and researched thermoplastic due to its excellent mechanical and physical properties, making it developed in the automotive sector, suitable for lighter vehicles, and, consequently, lower fuel consumption. This review manuscript presents the applications of PA-based materials in the manufacture of vehicle parts, with a description of their processing, a discussion about their thermal properties and the crystallization of polymer structure, the challenges of machining PA-based composite materials, and the feasibility of recyclability. This work aims to revise literature about the use of polyamide 6 (PA6), polyamide 66 (PA66), and polyamide 12 (PA12) and their composites reinforced with fiberglass (FG) and carbon fiber (CF) focused on the potential that these materials have as alternative materials for the automotive industry.

Abstract Polymer compatibilizer agents are crucial for industrial materials development. Compatibilizer agents may be prepared by melt-grafting in the reactive extrusion process which is cheaper and environmentally friendly. Maleic anhydride-grafted acrylonitrile-butadiene-styrene (ABS-g-MA) has emerged as a relevant compatibilizer agent for immiscible blends, like polycarbonate (PC)/ABS. In this work, ABS-g-MA was prepared by a simple reactive extrusion process using ABS, maleic anhydride (MA) and benzoyl peroxide (BPO). The MA:BPO ratios of 1:0.5 and 1:1 varying the content of MA by 1, 2 and 5 wt% were investigated. The grafting reaction was confirmed through Fourier transform infrared spectroscopy (FT-IR), grafted degree (GD%), thermal and rheological analysis. The effectiveness of the compatibilizer agent was evaluated in PC/ABS blends (70/30 and 85/15 blend ratios). The addition of 5 wt% of ABS-g-MA (5 MA:2.5 BPO) in the PC/ABS blends promoted an expressive reduction of ABS domain sizes and better dispersion in the PC matrix.

Abstract Antistatic packaging is a very important sector since the electrostatic discharge of electronic devices can damage and/or disable these products. In addition, it is essential to dispose of this packaging correctly. In this work, the synergistic effect of the addition of lignin and carbon black on the development of antistatic and biodegradable packaging was verified. In this study, PLA was mixed with lignin and carbon black and the composites were prepared using a high-speed thermokinetic homogenizer where the melting of the PLA and the blend with fillers occurred by friction. The composites were characterized by Izod impact tests, scanning electron microscopy, thermal properties, electrical characterization and biodegradation tests in garden soil. The results show that lignin is a great option to accelerate the biodegradation of PLA in the garden soil and the carbon black acts as an antistatic agent reducing the electrical resistivity of the composites.

In this work, polyaniline (PANI) in emeraldine-base form, synthesized by chemical oxidation polymerization, was protonated with hydrochloric acid (HCl). Composites based on high-density polyethylene (HDPE) and linear-low density polyethylene (LLDPE) blends with PANI were prepared in molten condition using a torque rheometer. The effect of compatibilizer agent (maleic anhydride-grafted high density polyethylene, HDPE-g-MA) and different contents of PANI on the blends-based composites was also investigated. Thermal, mechanical, and electromagnetic (electric permittivity) measurements and morphological aspects of the composites were evaluated. The addition of PANI content in the composites decreases the degree of crystallinity of HDPE and LLDPE blends, which implies that PANI particles make it difficult for co-crystallization to occur in the HDPE and LLDPE, respectively. On the other hand, the addition of compatibilizer agent in the HDPE and LLDPE blends increased the degree of crystallinity. The complex parameters of permittivity in the frequency range of 8.2 to 12.4 GHz varied as a function of the PANI content in the blend. It was also observed that the compatibilizer agent increased the composite stiffness and decreased the electric permittivity values. This result shows that the increasing rigidity of the molecular structure of the polyethylene matrix hindered the dissipation of the electromagnetic energy in the sample.

Epoxy/CNT and epoxy/CNT/calcium carbonate nanocomposites were produced via in situ polymerization assisted by ultrasonication without solvent and electrical, mechanical, thermal and thermomechanical properties of nanocomposites were evaluated. Epoxy/CNT presented very low percolation threshold, near 0.05 wt % and nanocomposites with higher contents of CNT presented further increase in electrical conductivity. The addition of calcium carbonate in epoxy/CNT nanocomposites increased the electrical conductivity, due to volume exclusion phenomena. Regarding thermal properties, due to the low content of the CNT and calcium carbonate no changes in glass transition (Tg) were observed. DMA results showed no significant changes in thermomechanical properties, once the contents of CNT and calcium carbonate are below stiffness threshold, however an increase of flexural modulus by adding CNT and calcium carbonate was observed.

Blends of ultra-high molecular weight polyethylene (UHMWPE) and different contents (0, 10, 20 and 30 wt%) of linear low-density polyethylene (LLDPE) with and without maleic anhydride-grafted LLDPE (LLDPE-g-MA) were prepared by melt blending and aging resistance, thermal and mechanical properties were evaluated. The degree of crystallinity increases with the content of LLDPE in the blends. On the other hand, the addition of compatibilizer agent modifies the crystallinity and the crystallite size. Non-compatibilized blends have excellent impact resistance properties and the addition of LLDPE-g-MA aids processing but decrease the impact resistance of the blends. Thermal and mechanical properties were greatly affected by thermal and water aging. The thermal aging leads to an increase in the degree of crystallinity and consequent a decrease in impact resistance.