Styrene butadiene rubber-organoclay nanocomposites were prepared with Cloisite 15A via melt intercalation. X-ray diffraction
and transmission electron microscopy indicated that the nanostructures are partially exfoliated and intercalated. The nanocomposites
exhibited great improvements in tensile strength and tensile modulus. The incorporation of organoclay gave rise to considerable
reduction of tan delta and increase in storage modulus in the rubbery region. It is shown that after 6 phr (parts per hundred
rubber) clay loading there is not much increase in the properties. The effect of carbon black (N330) on mechanical properties,
dynamic mechanical properties, heat build up, abrasion resistance in the nanocomposites having the optimized clay level (6
phr) was investigated. Optimum results were obtained with the addition of 25 phr carbon black. For comparison with the 6phr
nanoclay and 25phr N330 (high abrasion furnace carbon black) filled SBR composites, 40 phr N330 filled SBR composites was
used. The 6phr organoclay and 25phr N330 filled SBR nanocomposite showed better properties than 40phr carbon filled SBR compound.
These results indicate that 6phr organoclay can be replaced by 15 phr carbon black from the conventional SBR-carbon black
based tire tread compounds. The Dynamic mechanical analyzer (DMA) results revealed that the new tire tread compound gives
better rolling resistance and comparable wet grip resistance and lower heat build up than that of conventional tread compound. 相似文献
Cassava starch-filled natural rubber (NR) composites were prepared by using direct blending and co-coagulation method. The effects of two different method and cassava starch loading on morphology, mechanical properties and thermal properties of cassava starch/NR composites were studied. X-ray diffraction results and scanning electron microscopy images proved that co-coagulation method promotes better dispersion of cassava starch than direct blending method. The composites prepared by co-coagulation method exhibited higher values of tensile strength, tear strength, hardness, and thermal stability. The optimum value of tensile strength and tear strength of cassava starch/NR composites were achieved at a 10 phr cassava starch loading. 相似文献
Organoclay filled natural rubber (NR) nanocomposites were prepared using a laboratory two-roll mill. The effect of organoclay loading up to 10 phr was studied. The vulcanized nanocomposites were subjected to mechanical, thermal, and swelling tests. The results indicated that the tensile strength and elongation at break reached optimum at 4 phr of organoclay loading, and the incorporation of organoclay increased the tensile modulus and hardness of NR nanocomposites. The thermal degradation was shifted to a higher temperature and the weight loss decreased with incorporation of organoclay. Transmission electron microscopy (TEM) and X-ray diffraction (XRD) were employed to characterize the microstructure of NR nanocomposites. Results from TEM and XRD show the formation of intercalated and exfoliated individual silicate layers of organoclay filled NR nanocomposites particularly at low filler loading (< 4 phr). 相似文献
Summary: Three rubber‐based nanocomposites, natural rubber (NR), styrene‐butadiene rubber (SBR), and ethylene‐propylene‐diene rubber (EPDM) matrixes, were prepared with octadecylamine modified fluorohectorite (OC) by melt blending. X‐ray diffraction (XRD) revealed that the SBR/OC and EPDM/OC nanocomposites exhibited a well‐ordered intercalated structure and a disordered intercalated structure, respectively. In the case of the NR/OC nanocomposite, it exhibited an intermediate intercalated and even exfoliated structure. These results were in good agreement with transmission electron microscopy (TEM) observations. Furthermore, in the NR/OC and SBR/OC systems, the mixing process played a predominant role in the formation of nanometer‐scale dispersion structure, whereas the intercalated structure of EPDM/OC formed mainly during the vulcanization process. The tensile strength of SBR/OC and EPDM/OC nanocomposites loading 10 phr OC was 4–5 times higher than the value obtained for the corresponding pure rubber vulcanizate, which could be ascribed to the slippage of the rubber molecules and the orientation of the intercalated OC. For the strain‐induced crystallization NR, the exfoliated OC efficiently improved the modulus of the NR/OC nanocomposite relative to the pure NR. However, its hindrance on NR crystallization during the tensile process may be the main reason for the decrease in tensile strength of NR/OC.
XRD diffraction patterns of three nanocomposites containing 10 phr organoclay. 相似文献
Graphene oxide(GO) has recently attracted substantial interest as a possible reinforcing agent for next generation rubber composite materials. In this research, GO was incorporated in natural rubber(NR) composites through latex co-coagulation technique. The microstructures of GO/NR composites were characterized through a combination of transmission electron microscope, scanning electron microscope, X-ray diffraction, Fourier transform infrared spectroscopy, and Differential scanning calorimeter. The results showed that highly exfoliated GO sheets were finely dispersed into NR rubber matrix with strong interface interaction between GO and NR. The mechanical properties of the GO/NR composites were further evaluated. The results showed that the tensile strength, tear strength and modulus can be significantly improved at a content of less than 2 phr. Especially,GO exhibited specific reinforce mechanism in NR due to the stress-induced crystallization effects of NR. The stress transfer from the NR to the GO sheets and the hindrance of GO sheets to the stress-induced crystallization of NR were further displayed in stress–strain behavior of GO/NR composites. These enhanced properties were attributed to the high surface area of GO sheets and highly exfoliated microstructures of GO sheets in NR. 相似文献