Synthesis of High-Performance Lignin-Based Inverse Thermoplastic Vulcanizates with Tailored Morphology and Properties

We report synthesis of a high-strength renewable phenolic composition with linear large deformation strain without a thermoplastic-like yielding while retaining thermal processability. Small molecule carboxylic acid derivatives with varying molecular architectures act as esterifying crosslinkers in an equal mass mixture of lignin and acrylonitrile-butadiene copolymers in a highly scalable, solvent-free process. These inverse thermoplastic vulcanizates (iTPVs)-unique in their approach of crosslinking the rigid lignin phase rather than the soft phase-exhibit ordered self-assembly, tunable nanoscale morphology, and processability. The first of its kind iTPV compositions exhibit engineering stress- strain curves with two- to sixfold linear extensibility, a twofold rise in strength, and an order of magnitude enhanced modulus compared to a simple lignin-rubber blend. Viscoelastic properties correlate well with crosslinker architecture and the resulting morphology, allowing competing properties of toughness and stiffness to be tuned. This research finds a path for identifying the potential of lignin as a sustainable feedstock.

Automated summary

This research introduces a method for synthesizing a high-strength renewable phenolic composition with linear large deformation strain while maintaining thermal processability. Small molecule carboxylic acid derivatives are used as esterifying crosslinkers in a scalable, solvent-free process to mix lignin and acrylonitrile-butadiene copolymers. The resulting inverse thermoplastic vulcanizates show significant improvements in strength and modulus compared to a simple lignin-rubber blend, with tunable nanoscale morphology and enhanced processability.