Polymers

This study discusses the thermal behavior of glass fiber-reinforced SiO₂-filled polymers in dry milling. Focus is put on the effects of the addition of SiO₂ particles on cutting-generated heat and the fresh-surface integrity of the composite. Cutting trials were developed using a Spinner U-620 5-axis CNC machine. Real-time temperature histories owing to the dry milling of both Glass/Epoxy and Glass/Polyester composites were recorded using thermocouples preinstalled within the composite specimen. SEM inspections were conducted to elucidate the prevailing failure mechanisms during the material removal process. The results showed that fiber orientation significantly dominated thermal responses. Cutting perpendicular to the fiber orientation results in a critical temperature, while the addition of SiO₂ particles effectively reduces the temperature overlaps and peak values, causing the temperature to drop. The addition of SiO₂ serves to keep the temperature sufficiently lower than the glass transition point of the matrix. However, increasing the feed rate from 50 mm/min to 150 mm/min reduced the overall temperature during cutting. Under similar cutting conditions, Glass/Polyester composites exhibited lower peak temperatures and heat quantities than Glass/Epoxy regardless of the feed rate and fiber orientation. Observations revealed that fiber orientation and matrix type strongly influence the intensity of the thermal and mechanical damages induced. These findings suggest that the addition of silicon dioxide can adjust the thermal balance in dry cutting and may improve the composite’s structural integrity significantly. Such a composite design promotes the heat control of sensitive parts in advanced engineering applications.

Geopolymer materials obtained through the alkaline activation of fly ash represent a promising alternative for reducing the environmental impact of the construction sector, which is currently dominated by cement use. This study aimed to develop self-cleaning geopolymer composites by incorporating TiO₂ nanoparticles. Specimens containing 1%, 3%, and 4% TiO₂ were prepared using alkaline solutions based on Na₂SiO₃ and NaOH (6 M or 8 M), at mass ratios of 1:1 and 2:1. The results indicate that the three analyzed factors—the NaOH solution concentration, the activator ratio, and the nanoparticle dosage—significantly influence density, mechanical strength, and water absorption. Increasing the NaOH concentration to 8 M led to slight densification, improved flexural and compressive strength, and reduced water absorption. Modifying the Na₂SiO₃:NaOH ratio produced similar densification effects but resulted in reductions in mechanical strengths. The addition of 1–3% TiO₂ increased density and mechanical performance while reducing water absorption, whereas 4% TiO₂ content had the opposite effect. Self-cleaning capacity was confirmed by up to ~90% degradation of Rhodamine B after five UV–artificial rain–drying cycles, compared to only 27.3% degradation for the control samples.

This study investigates the degradation mechanisms of glass-fibre- and carbon-fibre-reinforced polymer (GFRP and CFRP, respectively) composites fabricated either with epoxy, vinyl-ester, or bio-epoxy resins under a hygrothermal environment. Composite laminates were manufactured using the vacuum-assisted resin infusion technique and exposed to high moisture and elevated in-service temperatures of 23 °C (room temperature), 40 °C and 60 °C for up to 125 days. Changes in the physical, microstructural, chemical and mechanical properties were then assessed. CFRP and GFRP composites showed distinct differences in their hygrothermal ageing depending on the resin system used in the manufacturing. CFRP composites consistently demonstrated higher stability than GFRP composites. Epoxy resin exhibited high resistance to water absorption and hydrolysis under hygrothermal exposure. After 125 days at 60 °C, glass/epoxy (GE) and carbon/epoxy (CE) composites retained 79.0% and 72.1% of their tensile strength and 46.9% and 72.6% of their interlaminar shear strength (ILSS), respectively. Vinyl-ester composites showed high mechanical retention, with glass/vinyl-ester (GV) and carbon/vinyl-ester (CV) retaining 70.8% and 83.1% of tensile strength and 67.5% and 80.3% of ILSS, respectively. Despite this mechanical stability, evidence of hydrolysis indicated ongoing chemical degradation of the vinyl-ester resin under prolonged hygrothermal exposure. In contrast, bio-epoxy composites exhibited relatively low overall durability. Glass/bio-epoxy (GB) retained 126.5% tensile strength and 68.8% ILSS, whereas carbon/bio-epoxy retained 61.0% tensile strength and 44.3% ILSS after 125 days at 60 °C. Overall, fibre and resin types were found to have a significant effect on the hygrothermal ageing of polymer composites.