TY - JOUR
T1 - Dielectric investigation of the molecular dynamics of blends (II)
T2 - polymers with dissimilar molecular architecture (PS/TMPC blend)
AU - Mansour, Ashraf A.
AU - Madbouly, Samy A.
PY - 1995/8
Y1 - 1995/8
N2 - The molecular dynamics of polystyrene/tetramethyl polycarbonate (PS/TMPC) blends were investigated using dielectric spectroscopy in the frequency and temperature ranges 10−2−107 Hz and 50–220°C, respectively. Blends with different compositions, namely 12.5, 25, 50, 75 and 87.5 wt% PS/TMPC were found to be compatible over the entire composition range and showed one glass relaxation process corresponding with the transition observed by calorimetric measurements. It was found that neither the kinetics or the distribution of relaxation times of the local process observed in pure TMPC were affected by blending. This fact implies that the local environment of the segments is not changed upon blending. Furthermore, these blends showed that the blending of TMPC with weakly polar polystyrene does not cause any change in the dipolar interaction of the TMPC segments, so that the relaxation strength varies linearly with composition. It is concluded that the polymeric chains of the TMPC and PS are not mixed at a segmental level, but at a higher structural level lying somewhere between segmental and molecular. This conclusion is in good agreement with that obtained in the case of blends composed of polymers with similar molecular architecture.
AB - The molecular dynamics of polystyrene/tetramethyl polycarbonate (PS/TMPC) blends were investigated using dielectric spectroscopy in the frequency and temperature ranges 10−2−107 Hz and 50–220°C, respectively. Blends with different compositions, namely 12.5, 25, 50, 75 and 87.5 wt% PS/TMPC were found to be compatible over the entire composition range and showed one glass relaxation process corresponding with the transition observed by calorimetric measurements. It was found that neither the kinetics or the distribution of relaxation times of the local process observed in pure TMPC were affected by blending. This fact implies that the local environment of the segments is not changed upon blending. Furthermore, these blends showed that the blending of TMPC with weakly polar polystyrene does not cause any change in the dipolar interaction of the TMPC segments, so that the relaxation strength varies linearly with composition. It is concluded that the polymeric chains of the TMPC and PS are not mixed at a segmental level, but at a higher structural level lying somewhere between segmental and molecular. This conclusion is in good agreement with that obtained in the case of blends composed of polymers with similar molecular architecture.
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U2 - 10.1002/pi.1995.210370405
DO - 10.1002/pi.1995.210370405
M3 - Article
AN - SCOPUS:84989741592
SN - 0959-8103
VL - 37
SP - 267
EP - 276
JO - Polymer International
JF - Polymer International
IS - 4
ER -