Title :
Influence of molecular orientation on polarization phenomena in polyethylene terephthalate films
Author :
Bernes, A. ; Chatain, D. ; Lacabanne, C.
Author_Institution :
Solid State Phys. Lab., Toulouse Univ., France
fDate :
6/1/1992 12:00:00 AM
Abstract :
A comparative study of the amorphous and crystallized unoriented polyethylene terephthalate (PET), uniaxially and biaxially oriented PET films has been performed by thermally stimulated current (TSC) spectroscopy. The study of TSC peak observed around the glass transition temperature (Tg) has been undertaken. Below T g a relaxation mode that seems to be a precursor of the glass transition is observed. The shift of the Tg peak towards higher temperature under stretching and crystallization indicates a stiffening of the amorphous chains. The analysis of the fine structure of the Tg peak has been done by using fractional polarization. The various elementary peaks correspond to relaxation times obeying a compensation law. At the compensation temperature Tc all the relaxation times become equal. The difference (Tc-Tg) is higher for the biaxially oriented PET. This behavior has been assigned to the existence of an important crystalline phase consecutive to biaxial orientation. This phase modifies the relaxation processes involved in the amorphous phase
Keywords :
crystallisation; dielectric polarisation; dielectric properties of solids; dielectric relaxation; glass transition (polymers); molecular orientation; polymer films; polymer structure; thermally stimulated currents; PET; TSC peak; amorphous; biaxially oriented; compensation law; compensation temperature; crystallization; crystallized unoriented; fractional polarization; glass transition temperature; molecular orientation; polarization phenomena; polyethylene terephthalate films; relaxation mode; uniaxially oriented; Amorphous materials; Crystallization; Glass; Optical films; Plastic films; Polarization; Polyethylene; Positron emission tomography; Spectroscopy; Temperature;
Journal_Title :
Electrical Insulation, IEEE Transactions on