Crystallization Behaviors and Regime Kinetics Analysis of Poly(<Emphasis Type="Italic">L</Emphasis>-lactide)-poly(butylene adipate)-poly(<Emphasis Type="Italic">L</Emphasis>-lactide) Based Multiblock Thermoplastic Polyurethanes

Poly(L-lactide)-based (PLLA) poly(ester-urethane)s are particularly relevant and gain significant attention due to their environment-friendly degradability and elastomeric shape memory capability. The tensile properties, resilience and degradation are strongly affected by their crystallization. This work was to investigate crystallization behaviors of the poly(L-lactide)-poly(butylene adipate)-poly(L-lactide) (PLLA-PBAPLLA) based thermoplastic polyurethane elastomers (PLAEUs) we synthesized previously. Dynamic scanning calorimetry (DSC) and polarized optical microscopy (POM) in combination with Avrami, Jezioney and Hoffman-Weeks models were used to analyze the impact of the PLLA block length on the crystallization temperature T_c, degree of crystallinity X_c, nucleation and spherulite growth mode and crystallization regime kinetics of the PLAEUs. The results indicate the low melting point poly(butylene adipate) (PBA) block resides in the amorphous domains while the PLLA block resides in both crystalline and amorphous phases. The X_c of the PLAEUs increase with the increased length of the PLLA block (i.e. higher content of PLLA block). The analyses with Avrami and Jezioney models show the PLAEU copolymers follow a disc-like spherulite growth. The covalently bonded PBA block decreases both nucleation velocity and spherulite growth rate in the isothermal crystallization. Such an impact is lessened as PLLA block length increases. The PLLA homopolymers demonstrate crystallization regime transition from II to III at a certain T_c of isothermal crystallization, while the crystallization regime kinetics of PLLA block in the PLAEUs are explained by a single regime III at low molecular weights of PLLA and the transition is restored as the PLLA block length increases (i.e. regime II to III).