Lignin-based
polyurethane elastomers (LPUe) with high stiffness,
strength, and toughness were facilely prepared by direct cross-linking
of unfunctionized lignin as hard segments and poly(propylene glycol)
tolylene 2,4-diisocyanate terminated (PPGTDI) as soft domains. The
effects of lignin molecular weight (3600 and 600 g mol–1) and weight fraction (5–40 wt %) on the thermal and mechanical
properties of LPUe were studied. With an increase in lignin content,
LPUe exhibited improved thermal stability, and the glass transition
temperature (T
g) also increased, especially
for LPUe derived from lignin with low lignin molecular weight of 600
g mol–1 (600-LPUe). Furthermore, LPUe also exhibits
excellent mechanical properties. For 600-LPUe with 40 wt % of lignin,
the Young’s modulus, tensile strength, and strain at break
reach 176.4 MPa, 33.0 MPa, and 1394%, respectively, which could be
attributed to better dispersion of low molecular weight lignin in
elastomers as evident from DSC, SEM, and TEM studies. Our results
demonstrate the potential application of unmodified lignin in developing
biobased high-performance PU materials. This is in contrast to many
current studies of LPUe systems that need lignin modification to prepare
PU materials.