A series of high-temperature thermoplastic elastomers (TPEs) and thermoplastic vulcanisates (TPVs) were successfully developed based on two different types of heat resistant polyamide (PA) (25 parts by weight)-PA-12 and PA-6, in combination with three different functionalized rubbers (75 parts by weight) of varying polarity, e.g., maleic anhydride grafted ethylene propylene diene terpolymer (MA-g-EPDM), sulphonated ethylene propylene diene terpolymer, and carboxylated acrylonitrile butadiene rubber, by melt mixing method. These rubbers have low level of unsaturation in its backbone, and the plastics showed high melting range. Thus, the developed TPEs and TPVs were expected to be high temperature resistant. Resol type resin was used for dynamic vulcanization to further increase the high temperature properties of these blends. Interestingly, initial degradation temperature of the prepared blends was much higher (421 8C for MA-g-EPDM/PA-12) than the other reported conventional TPEs and TPVs. Fourier transform infrared analysis described the interactive nature of the TPEs and TPVs, which is responsible for their superior properties. The maximum tensile strength with lowest tension set was observed for the carboxylated acrylonitrile butadiene rubber/PA-12 TPV. Mild increase in mechanical properties without any degradation was observed after recycling. Dynamic mechanical analysis results showed two distinct glass transition temperatures and indicated the biphasic morphology of the blends, as evident from the scanning electron microscopy.

No abstract

No abstract

This work aimed at studying the effect of a silica specific surface area (SSA), as determined by the nitrogen adsorption method, on the viscoelastic and fatigue behaviors of silica-filled styrene–butadiene rubber (SBR) composites. In particular, silica fillers with an SSA of 125 m2/g, 165 m2/g, and 200 m2/g were selected. Micro-computed X-ray tomography (µCT) was utilized to analyze the 3D morphology of the fillers within an SBR matrix prior to mechanical testing. It was found with this technique that the volume density of the agglomerates drastically decreased with decreasing silica SSA, indicating an increase in the silica dispersion state. The viscoelastic behavior was evaluated by dynamic mechanical analysis (DMA) and hysteresis loss experiments. The fatigue behavior was studied by cyclic tensile loading until rupture enabled the generation of Wöhler curves. Digital image correlation (DIC) was used to evaluate the volume strain upon deformation, whereas µCT was used to evaluate the volume fraction of the fatigue-induced cracks. Last, scanning electron microscopy (SEM) was used to characterize, in detail, crack mechanisms. The main results indicate that fatigue life increased with decreasing silica SSA, which was also accompanied by a decrease in hysteresis loss and storage modulus. SEM investigations showed that filler–matrix debonding and filler fracture were the mechanisms at the origin of crack initiation. Both the volume fraction of the cracks obtained by µCT and the volume strain acquired from the DIC increased with increasing SSA of silica. The results are discussed based on the prominent role of the filler network on the viscoelastic and fatigue damage behaviors of SBR composites.