Spherical CaCO3: Synthesis, Characterization, Surface Modification and Efficacy as a Reinforcing Filler in Natural Rubber Composites

Abstract

Natural rubber (NR), an important natural polymer derived from the Hevea brasiliensis tree, has been widely used in the rubber industry owing to its excellent elastic properties. However, it requires reinforcing fillers to improve its mechanical properties for the manufacturing of rubber products. Generally, calcium carbonate (CaCO3) is employed as a non-reinforcing filler. This work aimed to synthesize spherical-shaped CaCO3 at a submicrometric scale without and with surface treatment and explore its utilization as a reinforcing filler in NR composites. The morphological shape and polymorphic phase of CaCO3 were investigated using SEM, TEM, XRD, ATR-FTIR and Raman techniques. The mechanical properties of various amounts (0 to 60 phr) of CaCO3-filled NR composites were explored. As a result, the NR/treated CaCO3 composites provided higher tensile strength than the NR/untreated CaCO3 composites and pure NR at all filler loadings. This may have been due to the improved interfacial interaction between NR and CaCO3 with the improved hydrophobicity of CaCO3 after treatment with olive soap. The optimal filler loading was 20 phr for the highest tensile strength of the rubber composites. In addition, the elongation at break of the NR/treated CaCO3 was slightly decreased. Evidence from SEM and FTIR revealed the vaterite polymorph and shape stability of CaCO3 particles in the NR matrix. The results demonstrate that the particle size and surface treatment of the filler have essential effects on the mechanical property enhancement of the rubber composites. Synthesized spherical CaCO3 could be a potential reinforcing filler with broader application in polymer composites.

Thermal Oxidative Aging and Service Life Prediction of Commercial Ethylene–Propylene–Diene Monomer Spacer Damping Composites for High–Voltage Transmission Lines

“…The DTG curve depicted in Figure 2b demonstrates that the aging of EPDM had negligible influence on the degradation temperature. The third stage, observed within the temperature range of 650-750 • C, could be attributed to the thermal decomposition of CaCO 3 [33]. The residual substances included carbon black and the decomposition product of CaCO 3 and ZnO mineral additives.…”

“…temperature range of 650-750 °C, could be attributed to the thermal decomposition of CaCO3 [33]. The residual substances included carbon black and the decomposition product of CaCO3 and ZnO mineral additives.…”