Natural rubber from different Hevea braziliensis clones, namely RRIM600, RRIT251, PB235 and BPM24, exhibit unique properties. The influences of the various fresh natural rubber latex and cream concentrated latex on the non-rubber components related properties were studied. It was found that the fresh natural rubber latex exhibited differences in their particle size, which was attributed to the non-rubber and unique signature of clones which affect various properties. Meanwhile, the cream concentrated latex showed the protein contents, surface tension, and color of creamed latex to be lower than the fresh natural latex. However, TSC, DRC, viscosity, particle size and green strength of concentrated latex were found to be higher than the fresh natural latex. This is attributed to the incorporation of HEC molecules. Also, the rubber particle size distribution in the RRIM600 clone exhibited a large particle size and uniform distribution, showing good mechanical properties when compared to the other clones. Furthermore, the increased green strength in the RRIM600 clone can be attributed to the crystallization of the chain on straining and chain entanglement. These experimental results may provide benefits for manufacturing rubber products, which can be selected from a suitable clone.

A reprocessable elastomeric vulcanisate based on Epoxidised Natural Rubber with 50 mol-% epoxide content (ENR-50) was evloved by applying a self-assembled network based on thermochemically exchangeable ester crosslinks to the system. Hydrolysed Maleic Anhydride (HMA) as crosslinking substance in the presence of 1,2-DiMethylImidazole (DMI) as esterification accelerator and Zinc Acetate Dihydrate (ZAD) as transesterification catalyst was employed to generate the exchangeable ester crosslinking system. A sulphur-cured ENR-50 vulcanisate possessing a permanent sulphide crosslinking network was prepared as reference. Based on the results from cure characteristic and chemical structure analyses, the ENR-50 crosslinked with HMA behaves as a dynamic network because of a transesterification reaction catalysed by ZAD, promoting an exchangeable crosslinking network in the system. This dynamic network contributes to an intermolecular rearrangement of the ester crosslinking bonds at elevated temperatures, enabling interfacial self-adhesion and so reprocessability of the vulcanisates. The obtainable vulcanisates can be reprocessed, yielding relatively high retention of mechanical properties compared to their pristine counterpart. The interfacial self-adhesion and reprocessability of the vulcanisates have shown to significantly be improved with a higher loading of ZAD and elevated temperatures. This concept essentially shows a prospect towards developing e.g. novel recyclable and self-healing systems for elastomers.

This work aims to compare the performance between natural rubber (NR) composites with lead oxide (PbO) and bismuth oxide (Bi₂O₃) as shielding fillers for gamma radiation shielding applications. Modulus at 100% elongation, tensile strength, elongation at break, hardness and a specific gravity of the NR composites were investigated. The results indicated that NR/Bi₂O₃ and NR/PbO composites have no significant difference in terms of modulus and hardness values, while the NR/PbO composite exhibited better tensile strength and specific gravity than that of NR/Bi₂O₃ composite. However, NR/Bi₂O₃ composite exhibited better performance in oil resistance and thermal stability than the one with PbO. Gamma radiation shielding properties including mass attenuation coefficient ( ${\mu }_m$), effective atomic number (Z_eff), effective electron density (N_e) and half-value layer (HVL) have also been studied. It is seen that both the composites exhibited better radiation shielding properties. Furthermore, the radiation properties were in good agreement with the calculated theoretical values. In addition, both the composites of NR with PbO and Bi₂O₃ particles showed excellent radiation shielding properties compared to neat NR as well as commercially available materials including window, ordinary concrete and haematite-serpentine. The material developed in the present investigation can be used as efficient flexible radiation shielding materials. However, lead (Pb) is not suitable to use as a radiation shielding material due to its toxic nature to the human and the environment. Therefore, NR with Bi₂O₃ is an appropriate choice for producing novel wearable radiation shielding materials to manufacture gloves, aprons, rubber underwear and other wearable materials.

Flexible thermoplastic elastomers (TPE) were prepared for fused deposition modeling (FDM) or 3D printing. These materials can be used for medical purposes such as disposable soft splints and other flexible devices. Blends of 50% epoxidized natural rubber (ENR-50) and block rubber (Standard Thai Rubber 5L (STR5L)) with polycaprolactone (PCL) were produced and compared. The purpose of this study was to investigate the properties of natural rubber (NR) and PCL in simple blends with PCL contents of 40%, 50%, and 60% by weight (except at 75% for morphology study) in the base mixture (NR/PCL). The significant flow factors for FDM materials, such as melting temperature (T_m) and melt flow rate (MFR), were observed by differential scanning calorimetry (DSC) and via the melt flow index (MFI). In addition, the following mechanical properties were also determined: tensile strength, compression set, and hardness. The results from DSC showed that the melting temperature changed slightly (1–2 °C) with amount of PCL used, and there was a suspicious point in the 50/50 blends with both types of rubber. The lowest melting enthalpy of both blends was found at the 50/50 blended composition. The MFI results showed that PCL significantly affected the melt flow rate of both blends. The ENR-50/PCL blend flowed better than the STR5L/PCL blend. The conclusion was that this was due to the morphology of its phase structure having better uniformity than that of the STR5L/PCL blend. In compression set testing or measuring shape recovery, rubber directly influenced the recovery in all blends. The ENR-50/PCL blend had less recovery than the STR5L/PCL blend, probably due to the functional effects of epoxide groups and polarity mismatch. The hard phase PCL significantly affected the hardness of samples but improved shape recovery of the material. The ENR-50/PCL blend had better tensile properties than the STR5L/PCL blend. The elongation at break of both blends improved with a high rubber content. Hence, the ENR-50/PCL blend was superior to STR5L/PCL for printing purposes due to its better miscibility, uniformity, and flow, which are the keys to success for optimizing the fused deposition modeling conditions as well as the overall mechanical properties of products. Most blends in this study were only slightly different, but the 50/50 blend of ENR-50/PCL seemed to be near optimal for 3D printing.