Composites with sustainable natural fibers are currently experiencing remarkably diversified applications, including in engineering industries, owing to their lower cost and density as well as ease in processing. Among the natural fibers, the fiber extracted from the leaves of the Amazonian curaua plant (Ananas erectifolius) is a promising strong candidate to replace synthetic fibers, such as aramid (Kevlar™), in multilayered armor system (MAS) intended for ballistic protection against level III high velocity ammunition. Another remarkable material, the graphene oxide is attracting considerable attention for its properties, especially as coating to improve the interfacial adhesion in polymer composites. Thus, the present work investigates the performance of graphene oxide coated curaua fiber (GOCF) reinforced epoxy composite, as a front ceramic MAS second layer in ballistic test against level III 7.62 mm ammunition. Not only GOCF composite with 30 vol% fibers attended the standard ballistic requirement with 27.4 ± 0.3 mm of indentation comparable performance to Kevlar™ 24 ± 7 mm with same thickness, but also remained intact, which was not the case of non-coated curaua fiber similar composite. Mechanisms of ceramic fragments capture, curaua fibrils separation, curaua fiber pullout, composite delamination, curaua fiber braking, and epoxy matrix rupture were for the first time discussed as a favorable combination in a MAS second layer to effectively dissipate the projectile impact energy.

Graphene oxide (GO) incorporation in natural fiber composites has recently defined a novel class of materials with enhanced properties for applications, including ballistic armors. In the present work, the performance of a 0.5 vol % GO-incorporated epoxy matrix composite reinforced with 30 vol % fabric made of ramie fibers was investigated by stand-alone ballistic tests against the threat of a 0.22 lead projectile. Composite characterization was also performed by Fourier-transform infrared spectroscopy, thermal analysis and X-ray diffraction. Ballistic tests disclosed an absorbed energy of 130 J, which is higher than those reported for other natural fabrics epoxy composite, 74–97 J, as well as plain Kevlar (synthetic aramid fabric), 100 J, with the same thickness. This is attributed to the improved adhesion between the ramie fabric and the composite matrix due to the GO—incorporated epoxy. The onset of thermal degradation above 300 °C indicates a relatively higher working temperature as compared to common natural fiber polymer composites. DSC peaks show a low amount of heat absorbed or release due to glass transition endothermic (113–121 °C) and volatile release exothermic (~132 °C) events. The 1030 cm⁻¹ prominent FTIR band, associated with GO bands between epoxy chains and graphene oxide groups, suggested an effective distribution of GO throughout the composite matrix. As expected, XRD of the 30 vol % ramie fabric-reinforced GO-incorporated epoxy matrix composite confirmed the displacement of the (0 0 1) peak of GO by 8° due to intercalation of epoxy chains into the spacing between GO layers. By improving the adhesion to the ramie fabric and enhancing the thermal stability of the epoxy matrix, as well as by superior absorption energy from projectile penetration, the GO may contribute to the composite effective ballistic performance.

The coating of natural fiber by graphene oxide (GO) has, over, this past decade, attracted increasing attention as an effective way to improve the adhesion to polymer matrices and enhance the composite properties. In particular, the GO-functionalized 30 vol% curaua fiber (Ananas Erectifolius) reinforcing epoxy composite was found to display superior tensile and thermogravimetric properties as well as higher fiber/matrix interfacial shear strength. In this brief report, dynamic mechanical analysis (DMA) was conducted in up to 50 vol% GO-functionalized curaua fiber reinforced epoxy matrix (EM) composites. The objective was not only to extend the amount incorporated but also for the first time investigate the composite viscoelastic behavior. The GO functionalization of curaua fibers (GOCF) improved the DMA storage (E′) and loss (E″) modulus compared to the non-functionalized fiber composites. Values at 30 °C of both E′ (13.44 GPa) and E″ (0.67 GPa) for 50 vol% GO-functionalized curaua fiber reinforced epoxy matrix composites (50GOCF/EM) were substantially higher than those of 20 GOCF/EM with E′ (7.08 GPa) and E″ (0.22 GPa) as well as non-functionalized 50CF/EM with E′ (11.04 GPa) and E″ (0.45 GPa). All these results are above the neat epoxy previously reported values of E′ (3.86 GPa) and E″ (0.09 GPa). As for the tangent delta, the parameters associated with damping factor and glass transition temperature were not found to be significantly changed by GO functionalization, but decreased with respect to the neat epoxy due to chain mobility restriction.

Fiber-reinforced composites are among the most investigated and industrially applied materials. Many studies on these composites using fibers, especially with natural fibers, were made in response to an urgent action for ambient preservation. A particularly relevant situation exists nowadays in the area of materials durability. In this respect, no studies on water-immersion-accelerated aging in fique fiber–epoxy composites are reported. This work aimed to fill this gap by investigating the epoxy matrix composites reinforced with 40 vol% fique fabric. The epoxy matrix and the composite, both unaged and aged, were characterized by weight variation, water absorption, morphology, colorimetry (CIELAB method), Fourier transform infrared spectroscopy (FTIR) and dynamic–mechanical analysis (DMA). The main results were that degradation by water presents appearance of complex microfibril structures, plasticization of epoxy resin, and debonding of the fique fiber/epoxy matrix. The most intense color change was obtained for the water-immersion-aged epoxy by 1440 h. Cole–Cole diagrams revealed the heterogeneity of the materials studied.

Replacing synthetic fibers with natural ones as reinforcement in polymeric composites is an alternative to contribute to sustainability. Pineapple leaf fibers (PALF) have specific mechanical properties that allow their use as reinforcement. Further, graphene oxide (GO) has aroused interest due to its distinctive properties that allow the improvement of fiber/matrix interfacial adhesion. Thus, this work aimed to evaluate the ballistic performance and energy absorption properties of PALF-reinforced composites, presenting different conditions (i.e., GO-functionalization, and variation of fibers volume fraction and arrangement) through residual velocity and Izod impact tests. ANOVA was used to verify the variability and reliability of the results. SEM was employed to visualize the failure mechanisms. The Izod impact results revealed a significant increase in the absorbed energy with the increment of fiber volume fraction for the unidirectional configuration. The ballistic results indicated that the bidirectional arrangement was responsible for better physical integrity after the projectile impact. Furthermore, bidirectional samples containing 30 vol.% of GO non-functionalized fibers in a GO-reinforced matrix showed the best results, indicating its possible application as a second layer in multilayered armor systems.

Knowledge about the curing behavior of a thermosetting resin and its composites includes the determination of kinetic parameters and constitutes an important scientific and technological tool for industrial process optimization. In the present work, the differential scanning calorimetry (DSC) technique was used to determine several curing parameters for pure epoxy and its composite reinforced with 20 vol % mallow fibers. Analyses were performed with heating rates of 5, 7.5, and 10 °C/min, as per the ASTM E698 standard. The kinetic related parameters, that is, activation energy (E), Avrami’s pre-exponential factor (Z), and mean time to reach 50% cure (t½), were obtained for the materials, at temperatures ranging from 25 to 100 °C. Response surfaces based on the mathematical relationship between reaction time, transformed fraction, and temperature were provided for optimization purposes. The results showed that the average curing time used for the production of diglycidyl ether of bisphenol A/triethylenetetramine (DGEBA/TETA) epoxy systems or their composites reinforced with natural mallow fibers can be considerably reduced as the temperature is increased up to a certain limit.