Thermal strain-induced cold crystallization of amorphous poly(lactic acid)

Abstract

The cold crystallization behaviors and structure evolutions of amorphous PLA stretched within a high-temperature range (100–150 °C) were investigated via in situ synchrotron WAXS and SAXS measurements. The PLA stretched at 120 °C exhibits excellent mechanical properties with the highest modulus, stretching strength and moderate elongation, which is attributed to the coordination effect of thermally-induced initial crystallinity and moderate chain segment mobility. The WAXS results showed that the diffraction peaks of (200/110) and (203) planes shift to higher 2θ values, which indicates the formation of more ordered α′ and α forms during PLA stretching within 100–150 °C. More α forms can be formed from the stretched α′ form and/or from the amorphous phase at 100 °C. The phase diagram of α and α′ forms in stretched PLA with stretching temperature was proposed according to the obtained data of lattice spacing. The crystallinity of stretched PLA increases faster than that which underwent quiescent cold crystallization at the same temperature. The SAXS results indicated that the long period and lamellar thickness along and vertical to the stretching direction of PLA stretched within 100–150 °C exhibit distinct variations, which is attributed to the difference of strain-induced crystallization and lamellar orientation.