Abstract
We analyze thermally unstable lignin linkages that generate reactive sites and promote crosslinking reactions during thermal annealing at 180 °C. This results in significantly enhanced glass transition temperature (T g ). We use these characteristics of lignin to enhance interfacial reactivity of a lignin-based multiphase polymer synthesized by a dynamic shear process. An approximately 18 °C increase in T g and more than 230% increase in storage modulus (E') are achieved by thermally annealing the 50 wt% hardwood lignin-nitrile rubber composite for 5 h at 180 °C. Tunable chemical and physical crosslinks within lignin and rubber resulted in shape programmability demonstrating excellent strain recovery of the synthesized renewable materials. The substantial improvement of the elastic work density of the lignin-based elastomers allows a broader applicable stress window for stress/strain sensing. The renewable materials also exhibit a better strain recovery after thermal annealing.
Original language | English |
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Pages (from-to) | 210-222 |
Number of pages | 13 |
Journal | Polymer |
Volume | 160 |
DOIs | |
State | Published - Jan 3 2019 |
Funding
This research at Oak Ridge National Laboratory, managed by UT Battelle , LLC, for the U.S. Department of Energy under contract DE-AC05-00OR22725 , was sponsored by the Office of Energy Efficiency and Renewable Energy (EERE) BioEnergy Technologies Office (BETO) Program . C. C. B acknowledges the Wigner Fellowship Program as part of the Laboratory Directed Research and Development Program of Oak Ridge National Laboratory , managed by UT-Battelle, LLC, for the U.S. Department of Energy .
Funders | Funder number |
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U.S. Department of Energy | DE-AC05-00OR22725 |
Battelle | |
Office of Energy Efficiency and Renewable Energy | |
Oak Ridge National Laboratory | |
Bioenergy Technologies Office |
Keywords
- Elastomer
- Shape memory polymer
- Shear-induced crosslinking
- Thermal activation
- Thermo-responsive lignin