polyterpeen

Polyterpeen (also spelled polyterpene) denotes a class of polymers produced by the polymerization of terpene monomers, a family of hydrocarbon compounds commonly found in essential oils and plant resins. Typical monomers include isoprene, myrcene, limonene and pinene; the resulting materials range from elastomeric to thermoplastic depending on monomer identity, polymer architecture and degree of crosslinking.

Synthesis methods include free-radical, cationic and coordination polymerizations, as well as controlled/living techniques and ring-opening metathesis for certain terpene-derived precursors. Copolymerization with other dienes or vinyl monomers is widely used to tailor mechanical and thermal properties. Post-polymerization modifications (hydrogenation, epoxidation) further expand functionality and oxidative stability.

Physical properties of polyterpeens vary: some are soft, tacky resins used for adhesion and tack modification, while others form elastic rubbers suitable for tires, gaskets or damping components. They are generally hydrophobic and can exhibit low glass transition temperatures when derived from flexible monomers like isoprene.

Interest in polyterpeens has grown because terpenes are renewable, plant-derived feedstocks. Potential applications span adhesives, coatings, varnishes, specialty elastomers and biodegradable materials. Challenges include variability of natural feedstock composition, odor management and competitive cost versus petrochemical polymers. Environmental performance and end-of-life behavior depend on the specific polymer chemistry and formulation.