Phase Morphology and Mechanical Properties of Super-Tough PLLA/TPE/EMA-GMA Ternary Blends.

The inherent brittleness of poly(lactic acid) (PLA) limits its use in a wider range of applications that require plastic deformation at higher stress levels. To overcome this, a series of poly(l-lactic acid) (PLLA)/biodegradable thermoplastic polyester elastomer (TPE) blends and their ternary blends with an ethylene-methyl acrylate-glycidyl methacrylate (EMA-GMA) copolymer as a compatibilizer were prepared via melt blending to improve the poor impact strength and low ductility of PLAs. The thermal behavior, crystallinity, and miscibility of the binary and ternary blends were analyzed by differential scanning calorimetry (DSC). Tensile tests revealed a brittle-ductile transition when the binary PLLA/20TPE blend was compatibilized by 8.6 wt. % EMA-GMA, and the elongation at break increased from 10.9% to 227%. The "super tough" behavior of the PLLA/30TPE/12.9EMA-GMA ternary blend with the incomplete break and notched impact strength of 89.2 kJ∙m-2 was observed at an ambient temperature (23 °C). In addition, unnotched PLLA/40TPE samples showed a tremendous improvement in crack initiation resistance at sub-zero test conditions (-40 °C) with an impact strength of 178.1 kJ∙m-2. Morphological observation by scanning electron microscopy (SEM) indicates that EMA-GMA is preferentially located at the PLLA/TPE interphase, where it is partially incorporated into the matrix and partially encapsulates the TPE. The excellent combination of good interfacial adhesion, debonding cavitation, and subsequent matrix shear yielding worked synergistically with the phase transition from sea-island to co-continuous morphology to form an interesting super-toughening mechanism.

Recycling of sisal fiber reinforced polypropylene and polylactic acid composites: Thermo-mechanical properties, morphology, and water absorption behavior.

The effect of recycling on the thermo-mechanical and water absorption behavior of polypropylene (PP)/sisal fiber and polylactic acid (PLA)/sisal fiber composites were studied. The PP-based non-biodegradable composites and PLA-based biodegradable composites were recycled for four times. The effect of recycling was determined by examining the morphology, thermo-mechanical properties, and water absorption behavior and the obtained results were compared. The results showed that the incorporation of sisal fibers in the PP and PLA matrix enhances the tensile modulus and percentage crystallinity of the composites. The tensile strength and modulus of the sisal fiber reinforced PP composites were not affected with recycling. Even though the tensile properties of PLA and PLA/sisal fiber reinforced composites are superior to PP and PP/sisal fiber composites, the PLA-based composites show a dramatic decrease in tensile strength and modulus after the first recycling due to the degradation of the polymer. The thermal stability of the PP/sisal fiber composites was not affected by the repeated recycling process. On the other hand, the PLA-based composites with higher sisal fiber content show a bit lower thermal stability after recycling. The PP-based composites show fluctuations in percentage crystallinity with recycling. On the other hand, a remarkable increase in percentage crystallinity for PLA and PLA-based composites was observed with increasing recycling times. Water diffusion study divulges that the diffusion of water into the polymer composites was reduced with recycling, irrespective of the polymer matrix.