Abstract

The formation of shear bands and crazes in thin films as well as in bulk samples of polystyrene were examined in the electron microscope using a variety of replication techniques. The morphologies of shear bands and crazes are quite similar both depending initially upon the relative shear displacement of 400 to 1000 A domains. As deformation continues and orientation increases, fibrils varying from 50 to 700 A are formed within the deformation zone, lateral constraint of the normal Poisson contraction causing voids to form in the crazes but not in the shear bands. Shear-band width was found not to be a unique function of either temperature or strain-rate and both craze and shear-band morphologies were found not to be strong functions of molecular weight. Regardless of molecular weight, fibrils formed within the deformation zone were always on the order of a few hundred Angstroms in diameter. However, for thin films of molecular weight less than 20 000 insufficient numbers of tie molecules between fundamental structural units or domains made it difficult for these fibres to span the craze width.

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