01-06-2025 | Original Paper
Effect of SiO2 nanoparticles on the melt-crystallization kinetics and mechanical behavior of polypropylene
Authors: Ahmad A. Joraid, Mahdi A. Al-Maghrabi, Ali A. Alshehry
Published in: Journal of Polymer Research | Issue 6/2025
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Abstract
The article explores the significant effects of SiO2 nanoparticles on the crystallization kinetics and mechanical behavior of polypropylene (PP). Through extensive experimental analysis using differential scanning calorimetry (DSC), Raman and FTIR spectroscopy, polarized optical microscopy (POM), and mechanical testing, the study reveals how different concentrations of SiO2 nanoparticles influence the crystallization peak temperature, overall crystallization time, and enthalpy of PP. The findings indicate that low concentrations of SiO2 (0.5–1 wt%) markedly enhance nucleation, leading to improved crystallization kinetics and mechanical properties. The article employs various kinetic models, including JMAK, Ozawa, Mo, and Lauritzen–Hoffman, to provide a comprehensive understanding of the crystallization behavior under nonisothermal and isothermal conditions. The results show that SiO2 nanoparticles act as effective nucleating agents, reducing the crystallization time and activation energy, particularly at optimal concentrations. The mechanical properties, such as tensile strength, elongation at break, and Young’s modulus, are also significantly improved at low SiO2 concentrations, highlighting the potential of SiO2 nanofillers in optimizing PP composites for advanced applications. The study concludes that while low concentrations of SiO2 nanoparticles enhance the thermal and mechanical performance of PP, higher concentrations lead to nanoparticle agglomeration, which negatively impacts the material's properties.
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Abstract
This study investigates the effect of SiO₂ nanoparticles on polypropylene's (PP) crystallization kinetics and mechanical properties. SiO2 nanoparticles notably improve PP's thermal and mechanical performance by serving as nucleating agents, especially at lower concentrations. Differential scanning calorimetry (DSC) revealed that SiO2 nanoparticles delayed crystallization onset, prolonged induction times, and altered nucleation behavior. Using the Johnson–Mehl–Avrami-Kolmogorov (JMAK) model, it was observed that nanoparticles increased crystallization rates through enhanced heterogeneous nucleation. Conversely, aggregation restricted molecular mobility at higher nanoparticle loadings, adversely influencing crystallization and mechanical properties. Mechanical tests indicated that 0.5 wt% SiO2 significantly improved tensile strength (33.58 MPa) and elongation at break (41.3%). Excessive SiO2 loading led to nanoparticle agglomeration, reducing mechanical performance due to diminished stress transfer efficiency. Scanning electron microscopy (SEM) and Raman spectroscopy confirmed uniform nanoparticle dispersion and strong nanoparticle-polymer interactions at lower concentrations, whereas higher concentrations induced phase separation and structural inconsistencies. Furthermore, activation energy calculations using isoconversional methods, including Ozawa–Flynn–Wall (OFW) and Kissinger–Akahira–Sunose (KAS) models, demonstrated a progressive increase in activation energy with crystallization progress, indicating diffusion-limited crystallization at higher SiO₂ concentrations. The Mo model further confirmed SiO₂ nanoparticles' ability to lower the cooling rate necessary for achieving specific crystallinity levels. Overall, these findings highlight the potential of SiO₂ nanoparticles as effective additives for enhancing PP's mechanical performance and crystallization kinetics at optimal concentrations. The study provides valuable insights into the role of nanoscale fillers in polymer engineering, paving the way for advanced polypropylene-based nanocomposites with tailored thermal and mechanical properties.
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