Molecular orientation in polystyrene fibres has been studied using pol
arized Fourier transform infrared spectroscopy. Polymerization of the
monomers was carefully controlled to work with the same molecular weig
ht and heterogeneity index. During drawing, the velocity of the fibres
was maintained constant and the temperature was varied from 166 to 20
0-degrees-C. Samples were cut from the different fibres. Two polarized
spectra, with electric vectors parallel and perpendicular to the draw
ing direction, were recorded. The molecular orientation function was c
alculated from the area of the 1028 cm-1 peaks, which corresponds to t
he nu18a in-plane CH bending normal mode of the aromatic ring. Results
indicate that the molecular orientation depends strongly upon the dra
wing conditions. Annealing the fibre at a temperature slightly higher
than the glass transition temperature allows one to recover most of th
e isotropic properties.