In this work, a novel nanomaterial deposition technique involving the triboelectrification (TE) of glass fibers (GF) to create attractive charges on their surface was investigated. Through TE, continuous GF were positively charged thus, attracting negatively charged graphene oxide (GO) nanoparticles dispersed in a solution. The electrical charges on the glass fibers surface increased with the intensity of the TE process. The deposited GO coating was then chemically treated to obtain reduced graphene oxide (rGO) on the surface of GFs. The amount of coating obtained increased with the GO solution concentration used during the deposition process, as revealed by FESEM analysis. However, the same increment could not be noticed as a function of the intensity of the process. Both uncoated and coated GF were used to obtain single fiber microcomposites by using a bicomponent epoxy matrix. The fiber/matrix interfacial shear strength was evaluated through micro debonding tests, which revealed an increment of fiber/matrix adhesion up to 45% for rGO coated GF in comparison to the uncoated ones. A slight improvement in the electrical conductivity of rGO coated fibers through TE compared to conventional dip coating was also observed in terms of volumetric resistivity by a four-point probe setup.

In this study, novel biodegradable polycaprolactone (PCL)-based composites for sustainable packaging applications were developed by adding surface-treated wood fibers (WFs). Specifically, the WFs were treated with citric acid (CA) to improve the fiber/matrix adhesion and then melt compounded with a PCL matrix. The presence of an absorption peak at 1720 cm⁻¹ in the Fourier transform infrared (FTIR) spectra of CA-treated WFs, coupled with the increase in the storage modulus and complex viscosity in the rheological analysis, confirmed the occurrence of an esterification reaction between CA and WFs, with a consequent increase in interfacial interactions with the PCL matrix. Scanning electron microscopy (SEM) of the cryo-fractured surface of the composites highlighted that PCL was able to efficiently wet the fibers after the CA treatment, with limited fiber pull-out. Quasi-static tensile tests showed that the composites reinforced with CA-treated wood fibers exhibited a significant increase in yield strength (about 30% with a WF amount of 10% at 0 °C) and also a slight improvement in the VICAT softening temperature (about 6 °C with respect to neat PCL). Water absorption tests showed reduced water uptake in CA-treated composites, consistent with the reduced hydrophilicity confirmed by higher water contact angle values. Therefore, the results obtained in this work highlighted the potential of CA-treated WFs as reinforcement for PCL composites, contributing to the development of eco-sustainable and high-performance packaging materials.