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Filler–rubber composites were prepared by mixing chloroacetated natural rubber (CNR) with silica, carbon black (CB), or calcium carbonate using a two‐roll mill. The interactions between the CNR and fillers, including silica, carbon black, and calcium carbonate, were characterized based on glass transition temperature (Tg) and shear storage modulus (G′). The results showed that both the Tg and G′ values of the CNR‐Si composite were found to be higher than those of the CNR–CB and CNR–CaCO3 composites, indicating the existence of the CNR and silica interaction. The outstanding direct interaction between the CNR rubber matrix and silica without using a coupling agent was believed to be due to hydrogen bonds that formed between the hydroxyls of the silanol groups of silica and the carbonyls in the chloroacetate groups of CNR molecules. Moreover, it was also found that silica dispersed and distributed in the CNR matrix much better than in the natural rubber matrix. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016, 133, 43076.

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Dynamic vulcanization was studied in terms of the change in a-relaxation temperatures of the LDPE matrix, morphology, and mechanical properties of LDPE/ozonolysed NR blends which were vulcanized at various blend ratios and with different curing systems, i.e., peroxide and sulfur systems. The ozonolysed NR with M w ¼ 8.30 Â 10 5 g mol À1 and M n ¼ 2.62 Â 10 5 g mol À1 , prepared by the in situ ozonolysis reaction of natural rubber latex, was used in this study. The significant change in the a-relaxation temperature of LDPE in the LDPE/ozonolysed NR, dynamically vulcanized using the sulfur system, suggested that sulfur vulcanization of the blend gave a higher degree of crosslink density than using peroxide and corresponded with the improved damping property and homogenous phase morphology. However, the peroxide cured blends of LDPE/ozonolyzed NR gave more improvement of tensile strength and elongation at break than the sulfur cured system. Furthermore, the mechanical properties of tensile strength, elongation at break, and damping were improved by increasing the ozonolyzed natural rubber content in both DCP and sulfur cured blends.

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Green electrospinning technique was employed to prepare chloroacetated natural rubber (CNR)/poly(vinyl alcohol) (PVA) nanofiber films by varying the addition of PVA in the range 2.5–55 wt % followed by encapsulation of 2.5 wt % fumed silica (FS). In this study, the risk of using organic solvents was eliminated using CNR in latex. The encapsulated electrospun fiber mats showed a fairly homogenous composition with enhanced water absorption ability of 703.54% ± 33.95%. The FS improved the interfacial adhesion and contributed to enhancing the intermolecular interaction between the two polymers. The mean diameter of the nanofibers decreased from 64.0 ± 19.0 to 41.0 ± 13.0 nm and significant improvement in the hydrolytic and enzymatic degradation rate was observed implying that FS can facilitate the degradation rate. Furthermore, loading of PVA and encapsulation of FS resulted in an improved stiffness of CNR at room temperature and storage modulus increased to 2.48 and 2.12 MPa, respectively. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018, 135, 46432.

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