In thin amorphous polymer films, the entanglement density, v(c), stron
gly influences the draw ratio during micronecking and the competition
between cavitational and non-cavitational processes, often referred to
as crazing and shear deformation respectively. TEM investigations sug
gest this also to be true of polymers capable of crystallizing althoug
h modes of deformation involving chain slip may be suppressed owing to
strain induced crystallization. In either case, v(c) is determined no
t only by the intrinsic properties of the polymer in question (chain s
tiffness and packing density), but also by the sample history. In melt
crystallized semicrystalline films, for example, if crystallization t
akes place. relatively slowly compared with the rate of relaxation of
chain conformations in the melt, v(c) may be substantially reduced owi
ng to a decrease in chain interpenetration. Evidence for this comes fr
om observations of the draw ratios in micronecks in isotactic polyprop
ylene films isothermally crystallized at different temperatures, which
increase sharply in regimes where entanglement loss is predicted to o
ccur during crystallization.