Natural rubber (NR) is incompatible with hydrophilic additives like halloysite nanotubes (HNT) due to their different polarity. The silane coupling agent is the ideal component to include in such a compound to solve this problem. Many types of silane are available for polymer composites depending on their functionalities. This work aimed to tune it to the composite based on NR and HNT. Four different silanes, namely Bis[3- (Triethoxysilyl)Propyl]Tetrasulfide (TESPT), 3-Aminopropyl triethoxysilane (APTES), N-[3-(Trimethoxysilyl)Propyl] Ethylenediamine (AEAPTMS), and Vinyltrimethoxysilane (VTMS) were used. Here, the mechanical properties were used to assess the properties, paying close attention to how their reinforcement influenced their crystallization behavior after stretching. It was revealed that adding silane coupling agents greatly improved the composites' modulus, tensile strength, and tear strength. From the overall findings, AEAPTMS was viable for NR/HNT composites. This was in direct agreement with the interactions between NR and HNT that silanes had encouraged. The findings from stress-strain curves describing the crystallization of the composites are in good agreement with the findings from synchrotron wide-angle X-ray scattering (WAXS). The corresponding silanes have substantially aided the strain-induced crystallization (SIC) of composites.
Halloysite nanotubes (HNTs) are naturally occurring tubular clay made of aluminosilicate sheets rolled several times. HNT has been used to reinforce many rubbers. However, the narrow diameter of this configuration causes HNT to have poor interfacial contact with the rubber matrix. Therefore, increasing the distance between layers could improve interfacial contact with the matrix. In this work, Epoxidized Natural Rubber (ENR)/HNT was the focus. The HNT layer distance was successfully increased by a urea-mechanochemical process. Attachment of urea onto HNT was verified by FTIR, where new peaks appeared around 3505 cm-1 and 3396 cm-1, corresponding to urea's functionalities. The intercalation of urea to the distance gallery of HNT was revealed by XRD. It was also found that the use of urea-treated HNT improved the modulus, tensile strength, and tear strength of the composites. This was clearly responsible for interactions between ENR and urea-treated HNT. It was further verified by observing the Payne effect. The value of the Payne effect was found to be reduced at 62.38% after using urea for treatment. As for the strain-induced crystallization (SIC) of the composites, the stress-strain curves correlated well with the results from synchrotron wide-angle X-ray scattering.
Lignin from kenaf (Hibiscus cannabinus) core was investigated as an alternative filler for rubber. Three types of extraction methods were used to isolate lignin from kenaf, namely kraft, soda and organosolv process. The particle size, surface area, functionalities changes, molecular weight and thermal properties of the lignin were characterized. The results showed that Kraft lignin (KL) has the smallest particle size (40.41 μm) compared to soda lignin (SL) (63.85 μm) and organosolv lignin (OL) (66.85 μm). This is in good agreement with the BET surface area of 9.52 m2/g, 1.25 m2/g and 2.40 m2/g respectively. However, the smaller surface area of SL compared to OL is due to the smaller pore size and pore volume of SL. KL also showed high hydroxyl content with corresponding high thermal stability as confirmed by NMR and TGA. The thermal stability of the lignin correlates well with the molecular weight (MW). From the overall characteristics, it can be concluded that KL, SL and OL can be used as an alternative filler in rubber compounds to substitute common fillers like silica and carbon.
A massive demand for rubber-based goods, particularly gloves, was sparked by the emergence of the COVID-19 epidemic worldwide. This resulted in thousands of tons of gloves being scrapped due to the constant demand for the items, endangering our environment in a grave way. In this work, we aimed to focus on the utilization of waste nitrile gloves (r-NBR) as a component blended with natural rubber (NR). The life span and other related properties of the blend can be improved by proper control of the chemical recipe. This study assessed three types of crosslinking systems, namely sulfur (S), peroxide (DCP), and mixed sulfur/peroxide (S/DCP) systems. The results indicate that choosing S/DCP strongly affected the tensile strength of the blend, especially at relatively high contents of r-NBR, improving the strength by 40-60% for cases with 25-35 phr of r-NBR. The improvement depended on the crosslink types induced in the blends. It is interesting to highlight that the thermal resistance of the blends was significantly improved by using the S/DCP system. This indicates that the life span of this blend can be prolonged by using a proper curing system. Overall, the S/DCP showed the best results, superior to those with S and DCP crosslinking systems.