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Structure‐property relationships of blends of polycarbonate
Author(s) -
Cheah K.,
Cook W. D.
Publication year - 2003
Publication title -
polymer engineering and science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.503
H-Index - 111
eISSN - 1548-2634
pISSN - 0032-3888
DOI - 10.1002/pen.10146
Subject(s) - materials science , rheometry , polycarbonate , dynamic mechanical analysis , composite material , polymer blend , shear rate , glass transition , viscoelasticity , viscosity , polymer , thermodynamics , polymer chemistry , physics , copolymer
Three grades of bisphenol‐A polycarbonate—high molecular weight linear, high molecular weight branched and low molecular weight linear—and their blends have been studied by GPC, DMTA, DSC, rheometry and impact measurements. The molecular weight distribution of the blends agred with that predicted from the component's distributions, indicating that no transesterification reactions had occurred during melt blending. The T g of the blends varied with blend composition according to the Fox equation and was related to the reciprocal molecular weight predicted by the Flory‐Fox equation. The low shear rate viscosity of the blends agreed with a logarithmic rule of mixtures and showed power‐law dependence on the weight average molecular weight. At higher shear rates, shear thinning was observed. The steady shear viscosity correlated well with the dynamic viscosity, as suggested by the Cox‐Merz relation. The stress relaxation behavior of the melt was very sensitive to the blend composition and molecular weight and correlated well with the real modulus. Temperature studies of the dart impact energy showed that only the low molecular weight polymer underwent a brittle‐duetile transition at ea −30°C and that all the blends were tough at room temperature. The enhanced stress triaxiality inherent in the notched lzod test caused the impact strenght at room temperature to decrease almost linealy with blend composition.