Abstract
Vitrimers have been introduced to circumvent the lack of recyclability of traditional thermosets with permanent cross-linked structures, while preserving the advantages of structural stability and mechanical properties. The success of this lies in the successful incorporation of a robust networked structure to achieve reversible extensibility and toughness while preserving processability akin to thermoplastics. In this study, we report the synthesis of vitrimers utilizing 100% renewable and plant-based building blocks that exhibit transesterification exchange reaction (TER). The vitrimer was synthesized by solvent-free, high-shear reactive mixing of a biomass-derived lignin fraction enriched with carboxyl functionality and an epoxidized polyisoprene from natural rubber. The oxirane functionality in rubber reacts catalytically (zinc acetylacetonate) with carboxyl moieties in lignin to form esters at 180 °C. The ester linkages in the networked matrix undergo topological rearrangement upon heating above 180 °C, thus enabling (re)processability similar to thermoplastics. The material exhibits fast stress relaxation (characteristic relaxation time of <10 seconds) above 200 °C, which indicates the material's potential for use in rapid manufacturing of components and their recycling. This approach provides a pathway for circular and value-added utilization of lignin and subsequent use as a matrix for reinforced composites.
Original language | English |
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Pages (from-to) | 714-724 |
Number of pages | 11 |
Journal | Polymer Chemistry |
Volume | 15 |
Issue number | 8 |
DOIs | |
State | Published - Jan 29 2024 |
Funding
This work was supported by the U.S. Department of Energy, Office of Science, Basic Energy Sciences, Materials Sciences and Engineering Division [FWP# ERKCK60], under contract DE-AC05-00OR22725 with UT-Battelle, LLC. S. S. R. acknowledges doctoral research scholarship through the U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy (EERE), Vehicle Technologies Office (VTO).