The number of phases, transition temperatures, and microhardness of a
series of poly(ester ether carbonate) (PEEC) multiblock terpolymers wi
th poly(butylene terephthalate) (PET) hard segments have been investig
ated as a function of ether/carbonate (EC) soft-segment composition at
constant PET content. The polymerization degree of PET and the intrin
sic viscosity of the terpolymers were determined by viscosimetry. The
degree of crystallinity, long spacing, glass transitions T-g, and melt
ing temperature were derived by means of x-ray diffraction, dynamic me
chanical thermal analysis (DMTA), and differential scanning calorimetr
y (DSC) measurements. Surface mechanical properties were studied by mi
croindentation tests. It was found that the terpolymer consists of two
amorphous (EC and PET) phases and one crystalline (PET) phase. The T-
g value of PET does not depend on the chemical composition of the soft
segments, in the contrast to the T-g of the soft-segment amorphous ph
ase. Introduction of polycarbonate moities in the soft segments induce
s an increase of T-g by 50 degrees C without formation of an additiona
l (third) amorphous phase. The reduced crystallizability of PET hard s
egments (by;a factor of 3) is explained by this decrease of flexibilit
y of the soft segments, which also causes a twofold reduction in the m
icrohardness values. The dominating contribution of crystallinity to t
he microhardness is shown. However, the much lower measured overall mi
crohardness in contrast to the one calculated by means of the additive
law is explained by the plasticizing effect of the soft amorphous pha
se, This assumption is in agreement with the structure model derived f
rom the small-angle x-ray (SAXS) and wide-angle x-ray (WAXS) data.