Aa. Mansour et al., DIELECTRIC INVESTIGATION OF MOLECULAR-DYNAMICS OF BLENDS .3. EFFECT OF MOLECULAR-WEIGHT IN TMPC PS BLENDS/, Polymer international, 41(4), 1996, pp. 395-406
Dielectric and calorimetric measurements have been carried out for tet
ramethyl polycarbonate/polystyrene (TMPC/PS) blends with different com
positions. The effect of varying the molecular weight of the weakly po
lar component (PS) on the molecular dynamics of the polar segments of
TMPC has been thoroughly studied over wide ranges of frequency (10(-2)
-10(5) Hz), temperature (50-220 degrees C) and number average molecula
r weight, <(m)over bar (n)>, (6500-560 000 g mol(-1)). All blends were
found to be compatible regardless of the composition ratio and the mo
lecular weight of PS. Some new and interesting experimental findings h
ave been observed concerning the effect of molecular weight on the gla
ss temperature and on the broadness of the glass transition and relaxa
tion. Neither the kinetics nor the distribution of relaxation times of
the local process observed in pure TMPC was affected by blending with
PS, regardless of the composition ratio or the molecular weight of PS
. It has been concluded that the mixing of the polymeric components to
form a homogeneous single phase (compatible blend) does not take plac
e on a segmental level but on a structural one. The size of this struc
tural level has been suggested to have the same volume as the cooperat
ive dipoles, which is assumed to be the minimum volume responsible for
a uniform glass transition (10-15 nm). The molecular weight dependenc
e of the relaxation characteristics of the glass process and temperatu
re could be attributed to the variation in the size and packing of the
structural units.