Stress induced lamellar thickening in poly(ethylene succinate)

Abstract

The crystalline structure evolution of poly(ethylene succinate) during tensile deformation was investigated by in-situ synchrotron X-ray scattering. Crystal phase transition from α to β form was confirmed to be fully reversible upon stress loading and unloading. An increase of long period was observed during the α–β crystal transition, which was attributed to the increase of both amorphous layer thickness and crystalline layer thickness (lamellar thickness). The crystalline layer thickness was scaled with the fraction of β crystal, and the change of which was in well agreement with the difference in the repeating length along the crystallographic c axis. Both the crystalline layer thickness and the amorphous layer thickness were fully recoverable. A possible molecular model was proposed to visualize the mechanism for the crystal transition and lamellar thickening.