Most
biodegradable thermoplastic materials cannot be used as elastomers
due to their relatively poor elasticity. Poly(butylene furandicarboxylate-co-ε-caprolactone) (PBFCL) copolyesters were synthesized
from 2,5-furandicarboxylic acid (FDCA), 1,4-butanediol, and poly(ε-caprolactone)
diols. The PBFCLs are susceptible to hydrolysis and enzyme degradation,
and the degradation rate could be controlled by the enzymes. PBFCL40
and PBFCL50 (CL molar content) displayed high tensile strength (≥50
MPa), good elongation at break (≥1050%), and quick shape recovery
like an elastomer. Although BF and CL segments were incompatible,
the dynamic mechanical and rheological results excluded the possibility
of microphase separation under room temperature. In situ small-angle
X-ray scattering (SAXS) and wide-angle X-ray scattering (WAXS) measurements
revealed the evolution of crystals during stretching. Strain-induced
orientation, melting of original crystals, and formation of fibrillar
crystal occurred in different strain regions, and the surviving crystals
acted as the physical cross-linking points. This viewpoint was further
confirmed by measuring the recoverability during cyclic tensile tests
in PBFCL40 and PBFCL50 with controlled crystallinity. With controlled
crystallinity, samples gained adjustable elasticity.