The effects of the addition of epoxidized natural rubber/maleic anhydride-grafted polypropylene blend as a compatibilizing agent (CA) on the properties of natural rubber (NR)/polypropylene (PP) thermoplastic elastomer blend were studied. The blends were prepared in the molten state at 180°C using a Brabender Plasticorder at a rotor speed of 60 r min⁻¹. Evidence of compatibilization was obtained from the Brabender plastograms and from the mechanical properties results as well as the morphological analysis. It was found that the addition of the CA at different contents resulted in an increase of the tensile strength and Young’s modulus and a decrease of the elongation at break. It was also found that the melting temperature remained unchanged, the % crystallinity decreased, but the thermal stability was not affected. The morphology revealed a more homogeneous distribution of the dispersed PP phase for the CA-containing systems compared to the control NR/PP blend. These effects were attributed to the interactions that developed with the blend constituents through the functional groups of the CA.

This interesting study investigated the effect of Maleic Anhydride-grafted-Polypropylene/Epoxidized Natural Rubber (PP-g-MA/ENR) as a compatibilizing agent (CA) on the properties of a 30/70 Polypropylene/Natural Rubber PP/NR blends. The effect of dynamic vulcanization with sulfur-donors (i.e.: Tetramethyl thiuram disulfide (TMTD) and 4,4 Dithiodimorpholine (DTDM)) which were used as vulcanizing agents was also reported. Several formulations of TPVs with different concentrations of CA (from 5 to 15 phr) were prepared by mixing in the molten state using a Haake Rheocord 90. The structural analysis of dual compatibilizer was examined by FTIR spectroscopy. The rheological behavior was examined using Haake Rheocord 90. The mechanical properties were determined by the tensile measurements. The dynamic mechanical thermal properties were investigated by DMA. A morphological examination was conducted using SEM Microscopy, respectively. FTIR analysis confirmed reactions between the MA group in PP-g-MA and the epoxy groups in ENR, resulting in ENR-grafted PP with an ester and acid-based linkage. The Haake plastograms revealed a proportional increase in the final mixing torque value with the increasing content of CA. The mechanical results exhibited higher values in terms of tensile strength and Young’s modulus for the TPVs containing CA compared to un-compatibilized ones. The compatibilized TPV blends exhibited a noteworthy increase in storage modulus and a notable decrease in loss tangent values with the CA concentration increased. Furthermore, the TPVs show two distinct-phase morphologies. That is, the TPV with CA showed the presence of smaller vulcanized rubber particles dispersed within the PP matrix, a phenomenon that becomes more pronounced with higher CA contents.

This study investigates the effects of incorporating a 50/50 blend of Epoxidized Natural Rubber/Polypropylene-grafted maleic anhydride (ENR/PP-g-MA) as a compatibilizing agent (CA) for a 70/30 Natural Rubber/Polypropylene (NR/PP) thermoplastic elastomer (TPE) on the technical properties such as structural analysis, rheological, dynamic mechanical and morphological properties. Formulations with varying CA concentrations (5 to 15 phr) were prepared using a Brabender plasticorder at 180°C for 10 min. The structural analysis was examined by Fourier transform infrared spectroscopy (FTIR), and proton nuclear magnetic resonance (¹H-NMR). The rheological behavior was examined using a Rubber Process Analyser (RPA). The dynamic mechanical properties were investigated by DMA. Atomic Force Microscopy (AFM) was used for the morphological examination. FTIR analysis confirmed reactions between the MA group in PP-g-MA and the epoxy groups in ENR, resulting in ENR-grafted PP with an ester and acid-based linkage. This reaction was evident during compatibilizer preparation. RPA results showed increased viscosity for both types of CAs compared to their individual values, confirming crosslinking reactions. Higher CA concentrations led to elevated viscosity and storage modulus. DMA results indicated that the compatibilization led to a significant enhancement in the storage modulus of the blends. Moreover, an increase in the glass transition temperatures (Tg) of the blends was produced. AFM examination revealed a more homogenous distribution of the dispersed PP phase for the CA-containing blends compared to the control NR/PP system.

This study focuses on developing and characterizing high-density polyethylene (HDPE) composites with date seed (DS) fillers. Untreated DS (UDS) and alkali-treated DS (TDS) fillers were incorporated at 10, 20, and 30 wt% using two-roll mixing and compression molding, and their structural, rheological, mechanical, physical, and morphological properties were systematically characterized. Structural analysis by Fourier-transform infrared spectroscopy (FTIR) confirmed the removal of hemicellulose and lignin in treated fillers, enhancing filler–matrix compatibility. Rheological testing showed a decrease in melt flow index with increasing filler content, which was more pronounced in TDS composites due to stronger interfacial interactions. Mechanically, HDPE/TDS composites exhibited a ∼28% increase in tensile strength, a ∼35% improvement in Young’s modulus, and a ∼22% enhancement in impact resistance compared to neat HDPE. In contrast, elongation at break decreased, reflecting the trade-off between stiffness and ductility. Physically, water absorption decreased by nearly 65% in TDS composites compared to UDS counterparts, while density showed slight improvement due to reduced porosity and enhanced cohesion. Morphological analysis confirmed more homogeneous, uniform filler dispersion, and reduced agglomeration in TDS-based composites compared to HDPE/UDS composites. Overall, chemical treatment of DS significantly enhanced the structural, rheological, mechanical, and physical properties of HDPE composites. These findings demonstrate the potential of treated date seed as a sustainable reinforcement material for future industrial applications.