The isothermal crystallization of poly(ethylene terephthalate) (PET) homopolymers with different molecular weight was studied in a wide temperature range (140–230 °C) using different experimental techniques. Three different morphological regions, labeled
r1,
r2 and
r3, were distinguished as a
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The isothermal crystallization of poly(ethylene terephthalate) (PET) homopolymers with different molecular weight was studied in a wide temperature range (140–230 °C) using different experimental techniques. Three different morphological regions, labeled
r1,
r2 and
r3, were distinguished as a function of crystallization temperature (
Tc). In
r1 (low
Tc) crystallized samples were characterized by a low crystalline degree with a small spherulite texture containing thin crystals. In
r2 (intermediate
Tc) samples showed medium size spherulites composed of two distinct crystalline families (thin and thick crystals). In this temperature range, the crystallization exhibited a maximum value and it was associated with a high content of secondary crystals. In
r3 (high
Tc), samples presented considerable amorphous zones and regions consisting of oversized spherulites containing only thick crystals. Time-resolved wide-angle X-ray diffraction measurements, using synchrotron radiation, indicated a rapid evolution of the crystalline degree within the second region, in contrast with the quite slow evolution observed in the third region. On the other hand, by small-angle X-ray scattering (SAXS) and time-resolved SAXS experiment, it was found that the long period (
L) as well as the lamellar thickness (
lc) increase as a function of
Tc, corroborating the formation of the thickest crystals in the third region. From all these observations, a morphological model was proposed for each region.
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