a b s t r a c tA feasibility study was carried out on the utilization of Alkanolamide (ALK) on silica reinforcement of natural rubber (NR) by using a semi-efficient cure system. The ALK was incorporated into the NR compound at 1.0, 3.0, 5.0, 7.0 and 9.0 phr. An investigation was carried out to examine the effect of ALK on the cure characteristics and properties of NR compounds. It was found that ALK gave shorter scorch and cure times for silica-filled NR compounds. ALK also exhibited higher torque differences, tensile modulus, tensile strength, hardness and crosslink density of up to 5.0 phr of ALK loading, and then decreased with further increases of ALK loading. The resilience increased with increased ALK loading. Scanning electron microscopy (SEM) micrographs proved that 5.0 phr of ALK in the silica-filled NR compound exhibited the greatest matrix tearing line and surface roughness due to higher reinforcement level of the silica, as well as better dispersion and cure enhancement.

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This paper presents a comparison on the effects of blending chitin and/or starch with poly(lactic acid) (PLA). Three sets of composites (PLA–chitin, PLA–starch and PLA–chitin–starch) with 92%, 94%, 96% and 98% PLA by weight were prepared. The percentage weight (wt.%) amount of the chitin and starch incorporated ranges from 2% to 8%. The mechanical, dynamic mechanical, thermal and microstructural properties were analyzed. The results from the tensile strength, yield strength, Young’s modulus, and impact showed that the PLA–chitin–starch blend has the best mechanical properties compared to PLA–chitin and PLA–starch blends. The dynamic mechanical analysis result shows a better damping property for PLA–chitin than PLA–chitin–starch and PLA–starch. On the other hand, the thermal property analysis from thermogravimetry analysis (TGA) shows no significant improvement in a specific order, but the glass transition temperature of the composite increased compared to that of neat PLA. However, the degradation process was found to start with PLA–chitin for all composites, which suggests an improvement in PLA degradation. Significantly, the morphological analysis revealed a uniform mix with an obvious blend network in the three composites. Interestingly, the network was more significant in the PLA–chitin–starch blend, which may be responsible for its significantly enhanced mechanical properties compared with PLA–chitin and PLA–starch samples.

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In previous research, a polylactic chitin starch composite was prepared without the use of a solvent to enhance the miscibility. In this study, a polylactic acid (PLA) chitin starch composite was produced with chloroform as a plasticizer in the ratio 1:10. The blending of chitin and starch with PLA ranges from 2% to 8%. Tensile strength, impact, thermogravimetry analysis-Fourier-transform infrared spectroscopy (TGA)-FTIR, and differential scanning calorimetry (DSC) were used to test the thermomechanical properties. Also, the morphological properties, water absorption, and wear rate of the material was observed. The results showed that the tensile strength, yield strength, and impact strength were improved compared to the pure polylactic acid. Also, the elastic modulus of the samples increased, but were lower compared to that of the pure polylactic acid. The result of the fractured surface morphology showed good miscibility of the blending, which accounted for the good mechanical properties recorded in the study. The thermogravimetric analysis (TGA) and derivative thermogravimetric analysis DTA show a single degradation and peak respectively, which is also shown in the glass temperature measures from the DSC analysis. The water absorption test shows that the water absorption rate increases with starch content and the wear rate recorded sample A (92% P/8% C) as the highest. The high miscibility projected was achieved with no void, with the use of chloroform as a plasticizer.

In the new era of sustainable developments, various adaptations have been carried out in many industries to revolutionize the quest for sustainable materials as a method to reduce the dependency on petroleum feedstock. One of such inventions focusing on the automotive industries with new concepts of energy automotive such as electric and hybrid cars, as well as the utilization of inorganic materials as a components of polymer composites, which is expected to reduce the demand and utilization of various rubber composites in automotive parts. However, due to remarkable increment of service life and inherent properties, ethylene propylene diene terpolymer (EPDM) has showed the highest consumption in automotive segments and the fastest development rate in the field of polymer modification. Thus, a comprehensive review concerning the development of environmentally friendly EPDM-based composites reinforced by various clay minerals is highlighted and presented in this article. The characteristic of EPDM, including the chemistry, processing, properties, and applications, as well as the current research on various types of rubber/clay composites, EPDM/clay composites, and rubber/bentonite (Bt) composites, is reviewed and reported. In addition, the characteristics, properties, and applications of different types of clay minerals such as layered silicates, Bt clays, and montmorillonites as reinforcement material in EPDM composites are also included. Finally, the drawbacks and challenges in developments of EPDM/clay composites and the existing improvizations through various compatibilization of EPDM/clay composite system such as chemical modification of clays, functionalization using coupling agents, and compatibilization through grafting are discussed by highlighting the important findings.

The performance of rubber composite relies on the compatibility between rubber and filler. This is specifically of concern when preparing composites with very different polarities of the rubber matrix and the filler. However, a suitable compatibilizer can mediate the interactions. In this study, composites of natural rubber (NR) with halloysite nanotubes (HNT) were prepared with maleated natural rubber (MNR) and modified palm stearin (MPS) as dual compatibilizers. The MPS dose ranged within 0.5–1.5 phr, while the MNR dose was fixed at 10 phr in all formulations. It was found that the mixed MNR/MPS significantly enhanced modulus, tensile strength, and tear strength of the composites. The improvements were mainly due to improved rubber-HNT interactions arising from hydrogen bonds formed in the presence of these two compatibilizers. This was clearly verified by observing the Payne effect. Apart from that, the MPS also acted as a plasticizer to provide improved dispersion of HNT. It was clearly demonstrated that MNR and MPS as dual compatibilizers improved rubber-HNT interactions and reduced filler-filler interactions, which then improved tensile and tear strengths, as well as dynamical properties. Therefore, the mix of MNR and MPS had a great potential to compatibilize non-polar rubber with HNT filler.

Halloysite Nanotubes (HNT) are chemically similar to clay, which makes them incompatible with non-polar rubbers such as natural rubber (NR). Modification of NR into a polar rubber is of interest. In this work, Epoxidized Natural Rubber (ENR) was prepared in order to obtain a composite that could assure filler–matrix compatibility. However, the performance of this composite was still not satisfactory, so an alternative to the basic HNT filler was pursued. The surface area of HNT was further increased by etching with acid; the specific surface increased with treatment time. The FTIR spectra confirmed selective etching on the Al–OH surface of HNT with reduction in peak intensity in the regions 3750–3600 cm−1 and 825–725 cm−1, indicating decrease in Al–OH structures. The use of acid-treated HNT improved modulus, tensile strength, and tear strength of the filled composites. This was attributed to the filler–matrix interactions of acid-treated HNT with ENR. Further evidence was found from the Payne effect being reduced to 44.2% through acid treatment of the filler. As for the strain-induced crystallization (SIC) in the composites, the stress–strain curves correlated well with the degree of crystallinity observed from synchrotron wide-angle X-ray scattering.