Reactive
processing on conventional poly(ethylene terephthalate) (PET) with
the combination of pyromellitic dianhydride (PMDA) and triglycidyl
isocyanurate (TGIC) was used to produce long-chain branched PET (LCB-PET).
The branching factors of the PET samples were correlated from their
intrinsic viscosity and molar mass results. In all PET samples without
a cross-linked structure, PET modified with 0.1 wt % PMDA and 0.5
wt % TGIC (PET-P1T5) had the highest branching degree, with a branching
factor of 0.84. The relaxation time spectra of the three modified
PET samples with strain-hardening behaviors displayed rubbery states
during the relaxation process, which was ascribed to their increased
molecular weight or long-chain branched structure. Batch melt-foaming
experiments with CO2 were carried out to evaluate the melt-foamability
of PET. The results indicated that both a high molecular weight and
long-chain branched structure, especially the latter, could efficiently
lead to strong molecular entanglements and significantly improve the
polymer melt-foamability.