Heterogeneous blends of recycled poly(ethylene terephthalate) with impact modifiers: phase structure and tensile creep

Several types of photomicrographs have concurrently shown that impact modifiers (IMs) form particles (on a micrometre scale) which are evenly dispersed in a recycled poly(ethylene terephthalate) (PET) matrix; their adhesion to the latter is high enough that fracture surfaces (produced in liquid nitrogen) do not follow the interface. An essential part of the tensile creep of PET corresponds to the elastic time‐independent component; the time‐dependent component is rather limited, even if relatively high stresses are applied. Thus, the tensile compliance of PET is virtually independent of the applied stress, which indicates linear viscoelastic behaviour. The compliance of PET/IM blends (93/7, 90/10, 85/15 (by weight)) grows with the IM content and its time‐dependence becomes more visible. The effects of the two types of IM used in this study seem to be practically identical from the viewpoint of dimensional stability of the blends. The logarithm of compliance grows with the logarithm of time faster than linearly, and this tendency becomes more apparent with increasing fraction of IM. Even if the strain‐induced free volume is taken into account, a noticeable upswing of the compliance for longer creep periods (t > 1000 min) is evident. This cannot be interpreted as a consequence of the flow, because the recovery following the creep has proved the complete reversibility of the previous deformation. A simple empirical equation is proposed, which provides a plausible prediction of the creep behaviour of PET with dispersed impact modifiers. Copyright © 2004 Society of Chemical Industry