The beta relaxation of PET is studied as a function of its crystallini
ty. The variation of the magnitude of tan Phi is explained taking into
account the mechanical coupling of crystalline and amorphous phases b
y means of a series-parallel model which is intermediate between the p
urely parallel and series ones. The adjustable parameter which is cons
idered in such a model is related to the amorphous volume fraction whi
ch ensures the mechanical coupling and which appears to be propertiona
l to the reciprocal long period. The morphology analysis shows that th
e variation of the crystalline fraction (between 0.32 and 0.53) during
treatments carried out for one hour between 120 degrees C and 230 deg
rees C affects mainly the crystalline lamellae thickness while the lon
g period evolves much less. Therefore, the coupling fraction remains a
lmost unchanged. Moreover, an important feature of this work is that t
he beta relaxation in semicrystalline polymers does not linearly evolv
es with the crystallinity while beta relaxation does not exist in the
crystalline part.