Natural rubber latex foam (NRLF) was reinforced with micro- and nanofibrillated cellulose at a loading content of 5–20 parts per hundred of rubber (phr) via the Dunlop process. Cellulose powder from eucalyptus pulp and bacterial cellulose (BC) was used as a microcellulose (MC) and nanocellulose (NC) reinforcing agent, respectively. NRLF, NRLF-MC, and NRLF-NC exhibited interconnected macroporous structures with a high porosity and a low-density. The composite foams contained pores with sizes in a range of 10–500 µm. As compared to MC, NC had a better dispersion inside the NRLF matrix and showed a higher adhesion to the NRLF matrix, resulting in a greater reinforcement. The most increased tensile strengths for MC and NC incorporated NRLF were found to be 0.43 MPa (1.4-fold increase) and 0.73 MPa (2.4-fold increase), respectively, by reinforcing NRLF with 5 phr MC and 15 phr NC, whereas the elongation at break was slightly reduced. Compression testing showed that the recovery percentage was improved to 34.9% (1.3-fold increase) by reinforcement with 15 phr NC, whereas no significant improvement in the recovery percentage was observed with MC. Both NRLF-MC and NRLF-NC presented hydrophobic surfaces and good thermal stability up to 300 °C. Due to their highly porous structure, after a prolong immersion in water, NRLF composites had high water uptake abilities. According to their properties, the composite foams could be further modified for use as green absorption or supporting materials.

Natural rubber (NR), a long-chain hydrocarbon polymer mostly consisting of cis-1,4-polyisoprene units, has a high molecular weight (MW) and viscosity, enabling it to show excellent physical properties. However, NR has no reactive functional group, making it difficult to react with other molecules, especially in manufacturing processes. The functionalized low-molecular-weight NR (FLNR) is a requirement to disperse ingredients into the rubber adequately. Here, the FLNR was prepared by a photochemical degradation process under UVC-irradiation in the presence of H₂O₂ using P25-titanium oxide (TiO₂) powder as a photocatalyst. The optimum condition for the preparation of FLNR was the use of 2.0 g of TiO₂ powder per 100 g of rubber and H₂O₂ at 20% w/w under UVC-irradiation for 5 h. The hydroxyl groups were found on the NR chains due to the chain-scission of polyisoprene chains and hydroxyl radicals in the system. The weight average MW of NR decreased from 12.6 × 10⁵ to 0.6 × 10⁵ gmol⁻¹, while the number average MW decreased from 3.3 × 10⁵ to 0.1 × 10⁵ gmol⁻¹.