The crystallization kinetics of poly(butylene terephthalate) (PBT), poly(et
hylene terephthalate) (PET), and their copolymers poly(1,4-butylene-co-ethy
lene terephthalate) (PBET) containing 70/ 30, 65/35 and 60/40 molar ratios
of 1,4-butanediol/ethylene glycol were investigated using differential scan
ning calorimetry (DSC) at crystallization temperatures (T-c) which were 35-
90 C below equilibrium melting temperature T-m(o). Although these copolymer
s contain both monomers in high proportion, DSC data revealed for copolymer
crystallization behaviour. The reason for such copolymers being able to cr
ystallize could be due to the similar chemical structures of 1,4-butanediol
and ethylene glycol. DSC results for isothermal crystallization revealed t
hat random copolymers had a lower degree of crystallinity and lower crystal
lite growth rate than those of homopolymers. DSC heating scans, after compl
etion of isothermal crystallization, showed triple melting endotherms for a
ll these polyesters, similar to those of other polymers as reported in the
literature. The crystallization isotherms followed the Avrami equation with
an exponent n of 2-2.5 for PET and 2.5-3.0 for PBT and PBETs. Analyses of
the Lauritzen-Hoffman equation for DSC isothermal crystallization data reve
aled that PBT and PET had higher growth rate constant G(o), and nucleation
constant K-g than those of PBET copolymers. (C) 2001 Society of Chemical In
dustry.