This study demonstrates improved impact resistance and dynamic behavior in bioelastomers from terpenes, suggesting new sustainable materials for industrial applications.
The increasing demand for sustainable materials has propelled the development of bio-based elastomers derived from renewable terpenes. This study presents the synthesis of high-cis poly(butadiene-co-terpene) copolymers using coordination chain transfer polymerization with neodymium-based catalysts, enabling precise control of molecular weight and microstructure. Two terpene monomers, β-myrcene and trans-β-farnesene, were incorporated up to 45 wt% without compromising the elastomeric 1,4-cis polybutadiene segments. The copolymers were evaluated as impact modifiers in acrylonitrile–butadiene–styrene (ABS) and as vulcanizable rubber formulations. ABS containing bio-based copolymers exhibited distinct rubber morphologies, including elongated and rod-like particles with average particle diameters greater than 1042 nm and rubber phase volume fraction values ≥ 0.49, resulting in improved impact resistance exceeding 580 J/m and elongation at break higher than 12%. Vulcanized rubbers incorporating terpene segments displayed tunable curing kinetics, mechanical properties, and dynamic mechanical behavior, with notable increases in elongation (up to ~520%) and elasticity attributed to lower crosslink density (<1.20 × 10−4 mol/mL). Additionally, its energy dissipation capacity has been enhanced compared to the high-cis polybutadiene. These findings highlight the potential of terpene-derived bioelastomers as sustainable alternatives to fossil-based rubbers, offering comparable or enhanced performance for engineering polymer applications. The study underscores important structure–property relationships, providing a foundation for further optimization toward industrial adoption.
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Magaña et al. (2025) studied this question.
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