Polymer concepts in microscopically‐viewed phase transition behavior of crystalline polymers

Abstract

AbstractStructural evolution process in crystalline phase transition, isothermal crystallization from melt and solvent‐induced crystallization has been investigated for crystalline polymers on the basis of the time and/or temperature dependence of small‐angle X‐ray scattering (SAXS), wide‐angle X‐ray scattering (WAXS) and infrared/Raman spectra. As examples of isothermal crystallization study, polyethylene and polyoxymethylene were investigated. As for polyoxymethylene, the time‐resolved infrared spectral measurement clarified the appearance of infrared bands characteristic of folded chain crystal (FCC) in the early stage of crystallization process, followed by the detection of infrared bands characteristic of extended chain crystal (ECC) in a later stage. From the time‐resolved SAXS measurement, the stacked lamellar structure of ca. 14 nm long period was detected at first and it was followed by an appearance of the new lamellae in the amorphous region sandwiched between the original lamellae, resulting in the tightly stacked lamellar structure of 7 nm long period. The timing of detecting the SAXS 14 nm peak was almost the same with the observation of infrared FCC bands and the SAXS 7 nm peak with the infrared ECC band. This correspondency allowed us to speculate that some chains bridging several lamellae became fully extended when the new lamellae were formed in the amorphous region sandwiched between the original lamellae. As a result the ECC‐like structural parts were formed, giving the ECC infrared bands. As other examples, the Brill transition of aliphatic nylons and the solvent‐induced crystallization of syndiotactic polystyrene have been reviewed.