This article examines the influence of micro- and nanoscale calcium carbonate (CaCO3) fillers on the dielectric behavior and aging resistance of polyvinyl chloride (PVC)-based composites. PVC films containing varying CaCO3 contents (0%, 2.5%, 5%, and 7.5% by weight) were subjected to accelerated aging through prolonged ultraviolet (UV) exposure and thermal stress for up to 1248 h. The evolution of dielectric properties was characterized by impedance spectroscopy, while structural modifications were analyzed using Fourier-transform infrared (FTIR) spectroscopy. Additionally, changes in surface morphology, internal homogeneity (related to particle size, shape, and distribution), and chemical composition were investigated using scanning electron microscopy combined with energy-dispersive X-ray spectroscopy (SEM-EDX), to evaluate the effects of irradiation and variations in the material’s surface composition and morphology. The results reveal a significant correlation between filler concentration and dielectric stability, highlighting the potential of CaCO3 reinforcement to improve the long-term reliability of polymeric insulating materials. The results further highlight that beyond the amount of filler used, the fine-scale feature of CaCO3, particularly its particle size and how well it is dispersed, has a significant impact on how the material responds to aging and maintains its dielectric properties.
This study investigated the effect of nanofiller on the structural properties of thermally aged polyvinyl chloride (PVC)/Aluminum oxide (Al2O3) nanocomposites prepared with different amounts of nanoparticles (2.5, 5.0, and 7.5 wt%) using various techniques. Experimental studies were designed to monitor structural changes in PVC/Al2O3 nanocomposites by means of dielectric characterization, charging and discharging currents measurements, SEM and FTIR analyses, and visual observations as a function of nanofiller amount and aging time. The results obtained demonstrated that the dielectric permittivity of PVC was increased for unaged samples with the addition of 2.5% and 7.5% Al2O3 nanoparticles. An increase in dielectric losses is also observed at the same level of filler content, attributable to interfacial polarization driven by improved charge transport and dipole relaxation. A decrease in charging and discharging currents with higher Al2O3 content is attributed to an increase in matrix rigidity, which restricts charge carrier mobility. The charging and discharging currents progressively increased during thermal aging, as polar aging products were formed during this process, which could improve charge mobility and conductivity. FTIR and SEM analyses indicated that with thermal aging, polar groups formation was more likely due to structural decomposition of the matrix and mild dehydrochlorination. The changes in color were indicative of surface degradation. These results provide new insight into the electrical and aging behaviors in PVC/Al2O3 nanocomposites.
This study provides an in-depth investigation of the influence of calcium carbonate (CaCO3) filler on the mechanical performance and aging resistance of polyvinyl chloride (PVC)-based composites. PVC/CaCO3 composites containing 2.5, 5, and 7.5 wt% of CaCO3 were subjected to accelerated aging under combined ultraviolet (UV) irradiation and thermal stress for up to 1248 h. The key mechanical properties of specimens —tensile strength and elongation at break—were measured before and after aging. Changes in surface morphology, coloration, hydrophobicity, and chemical composition were characterized using scanning electron microscopy (SEM-EDS), X-ray spectroscopy, atomic force microscopy (AFM), contact angle measurements, and carbonyl index calculation to quantify relationships between the structural and physical properties of the specimens and aging conditions. The results reveal a significant correlation between filler content and the mechanical behavior of aged specimens, highlighting the potential of CaCO3 reinforcement not only to improve the retention of mechanical properties but also to increase the service life of PVC-based insulation compounds.