AbstractThe microdeformation morphology of a number of vinyl polymers with bulky side chains (type I) and arylene polymers with flexible oxygen linkages (type II) was studied by electron microscopy. The polyarylenes crazed only near the glass transition while the polyvinyls exhibited a crazing regime that extended to liquid nitrogen temperatures. In addition significantly less plastic strain was localized in type II glass crazes relative to those in type I glasses. In compatible blends of polystyrene (PS) and 2,6‐dimethyl poly(phenylene oxide) (2MPPO), ca. 30 2MPPO was sufficient to induce a transition from type I to type II crazing behavior. Small amounts of PS suppressed the low‐temperature 2MPPO β relaxation but enhanced the intermediate transition of 2MPPO at higher temperatures. Blending increased the conformational energy of the 2MPPO chain and improved interchain packing. The propensity for the polymer glass to form sharp shear bands at the expense of diffuse bands was increased by a decrease in the conformation energy of the polymer chain and an improvement in the glassy state pac
展开▼
