The insufficient molecular weight of linear poly(butylene
adipate-co-terephthalate) (PBAT) leads to poor foamability
and mechanical
performance of foams, which seriously restricts the industrial application
of PBAT as foam materials. Herein, biobased itaconic anhydride was
grafted onto PBAT backbone, and then epoxidized soybean oil was added
to obtain a dynamic cross-linked network based on Zn(II)-catalyzed
transesterification. The rheology results showed that the storage
modulus and viscosity of the PBAT vitrimers increased obviously, exhibiting
a viscous liquid-like to elastic solid-like transition behavior with
increasing cross-linked degrees. Reversible cleavage of the cross-links
and reformation of the integrated cross-linked network through rebonding
of the dynamic bonds were observed under shears of alternative large-
and low-amplitude oscillations, endowing PBAT vitrimers with fluidity
and elasticity during processing. PBAT vitrimers exhibited strain-hardening
behavior in an extensional flow and could be foamed by supercritical
carbon dioxide foaming. The lightweight foam could show an expansion
ratio of up to 26.7-fold and a density of 0.045 g/cm3.
On coupling the cell structure and mechanical properties contributed
by the dynamic cross-linked network, the foams showed enhanced elasticity,
specific compressive strength, and damping properties. The strategy
of altering the viscoelasticity and mechanical properties of PBAT
simultaneously by a dynamic cross-linking network provides a new approach
toward obtaining high-performance PBAT foams.