Brittle-to-Ductile Transition of Sulfonated Polystyrene Ionomers

This study examines the brittle-to-ductile transition of sulfonated polystyrene ionomers (SPS) with different counterions. The polystyrene precursor was unentangled and had two ionic groups per chain on average. Thus, its terminal relaxation time was comparable to the lifetime of the associating ionic groups. Three types of ionomer samples were used to tune the association lifetime: (1) fully neutralized SPS with different alkali-metal counterions, (2) fully neutralized SPS with mixed sodium and cesium counterions, and (3) partially neutralized SPS with sodium or cesium counterions. For all three systems, the brittle-to-ductile transition could be represented by a diagram of two Weissenberg numbers, Wi and Wi(R), defined with respect to the terminal and Rouse relaxation times, respectively. A flowable region existed at sufficiently low Wi, independent of Wi(R). At higher Wi, a brittle-to-ductile transition of the ionomer melt occurred above a critical value of Wi(R). To achieve ductility during the application of rapid elongational flow, the Rouse-type motions should be sufficiently slow relative to the rate of ion-dissociation, so that the strain-induced breakup of the ionic cross-links would not cause very strong chain retraction that may further lead to the macroscopic fracture.

Automated summary

This study investigates the brittle-to-ductile transition of sulfonated polystyrene ionomers with different counterions. It was found that a flowable region existed at sufficiently low Wi, independent of Wi(R), while a brittle-to-ductile transition of the ionomer melt occurred at higher Wi, above a critical value of Wi(R). The study suggests that to achieve ductility during rapid elongational flow, Rouse-type motions should be slow relative to the rate of ion-dissociation.