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The industrial application of continuous glass fabric-reinforced polymer composites (GFRPCs) is growing; however, the manufacturing boundedness of complex structures and the high cost of molds restrict their use. This research proposes a three-dimensional (3 D) printing process for GFRPCs that allows low-cost and rapid fabrication of complex composite parts.

The composite is manufactured using a digital light processing (DLP) based Vat-photopolymerization (VPP) process. For the composites, suitable resin material and glass fabrics are chosen based on their strength, stiffness, and printability. Jacob's working curve characterizes the curing parameters for adequate adhesion between the matrix and fabrics. The tensile and flexural properties were examined using UTM. The fabric distribution and compactness of the cured resin were analyzed in scanning electron microscopy.

The result showed that the object could print at a glass fabric content of 40 volume%. In DLP-based VPP printing technology, the adequate exposure time was found to be 30 seconds for making a GFRPC. The tensile strength and Young's modulus values were increased by 5.54 and 8.81 times, respectively than non-reinforced cured specimens. The flexural strength and modulus were also effectively increased to 2.8 and 3 times more than the neat specimens. In addition, the process is found to help fabricate the functional component.

The experimental procedure to fabricate GFRPC specimens through DLP-based AM is a spectacular experimental approach.

The purpose of this paper is related with the comparative study between graphene-based glass fiber–reinforced polymer composites and without graphene composite on polymer matrix. The current study explains the result of amalgamation of 4 Wt.% graphene oxide (GO), in comparison to without graphene, on the mechanical strength of glass fiber/epoxy (GE).

A hand layup technique is used for the experimental study. For this, chemical synthesis process is approached based on Hummer’s theory. For mechanical testing of glass fiber–reinforced graphene composites and without graphene composites, American Society for Testing and Materials-3039 (ASTM3039) standards was adopted. Furthermore, comparatively, composites were characterized by field emission scanning electron microscopy.

Reinforcement of 4.0 Wt.% GO in epoxy matrix material showed 7.46% and 12.31% improvement in mechanical strength and elongation, respectively. Scanning electron microscopy results showed the influence of graphene cumulations in the failure of GO-reinforced GE (GO-GE) composites.

The inimitable things of graphene grounded nanofillers have encouraged in the world of material for their thinkable manipulation in glass fiber polymeric composites. In this work, for the first time, graphene is used as nanofiller in glass fiber epoxy coatings, and their fractography study is investigated.

This study aims to deal with both the development and mechanical investigations of unsaturated polyester matrix (UPR) composites containing recycled polyethylene terephthalate (PET) fibers as new fillers.

UPR/PET fibers composites have been developed as mats by incorporating 5, 8, 13 and 18 parts per hundred of rubber (phr) of 6-, 10- and 15-mm length PET fibers from the recycling of postconsumer bottles. The mechanical and physical properties of the composites were investigated as a function of fiber content and length. A significant increase in stress at break and in ultimate stress (sr) were observed for composites reinforced with 5 and 8 phr of 15-mm length PET fibers. The Izod impact strength of UPR/mat PET fiber composites as a function of fiber rate and length showed that the 5 and 8 phr composites for the 15-mm length PET fiber have the optimal mechanical properties 13.55 and 10.50 Kj/m², respectively. The morphological study showed that the strong adhesion resulting from the affinity of the PET fiber for the UPR matrix. The ductile fracture of materials reinforced with 5 and 8 phr is confirmed by the fiber deformation and fracture surface roughness.

This study concluded that the PET fiber enhances the properties of composites, a good correlation was observed between the results of the mechanical tests and the structural analysis revealing that for the lower concentrations, the PET fibers are well dispersed into the resin, but entanglements are evidenced when the fiber content increases.

It can be shown from scanning electron microscopy micrographs that the fabrication technique produced composites with good interfacial adhesion between PET fibers and UPR matrix.