Use of maleic anhydride compatibilization to improve toughness and other properties of polylactide blended with thermoplastic elastomers

Polylactide (PLA) being a very brittle biopolymer could be toughened by blending with thermoplastic elastomers such as thermoplastic polyurethane elastomer (TPU) and thermoplastic polyester elastomer (TPE); unfortunately, these blends are immiscible forming round domains in the PLA matrix. Therefore, the purpose of this study was to investigate the effects of using maleic anhydride (MA) compatibilization on the toughness and other properties of PLA blended with TPU and TPE. MA grafting on the PLA backbone (PLA-g-MA) was prepared separately by reactive extrusion and added during melt blending of PLA/thermoplastic elastomers. IR spectroscopy revealed that MA graft might interact with the functional groups present in the hard segments of TPU and TPE domains via primary chemical reactions, so that higher level of compatibilization could be obtained. SEM studies indicated that PLA-g-MA compatibilization also decreased the size of elastomeric domains leading to higher level of surface area for more interfacial interactions. Toughness tests revealed that Charpy impact toughness and fracture toughness (K-IC and G(IC) of inherently brittle PLA increased enormously when the blends were compatibilized with PLA-g-MA. For instance, G(IC) fracture toughness of PLA increased as much as 166%. It was also observed that PLA-g-MA compatibilization resulted in no detrimental effects on the other mechanical and thermal properties of PLA blends. Copyright (c) 2014 John Wiley & Sons, Ltd

Loss of thermoplastic elastomer toughening in polylactide after weathering

It has been already pointed out that one of the best ways to increase toughness of the inherently brittle polylactide (PLA) without sacrificing strength and modulus is the use of thermoplastic elastomer toughening approach; but what happens under outdoor conditions was not explored. Therefore, the objective of this study was to explore the degree of losses especially in fracture toughness of PLA when blended with thermoplastic polyurethane (TPU) elastomer or thermoplastic polyester elastomer (TPE) after weathering. For this purpose, neat PLA, its 10 phr TPU and TPE blends were exposed to accelerated weathering conditions of both ultraviolet-irradiation cycles and moisture cycles as described in the standard of ISO 4892-3 for various periods. In general, due to the significant molecular weight reduction via chain scission reactions, drastic losses in the strength and toughness of the specimens were observed. On the other hand, in terms of %retention in the properties after weathering periods, it could be suggested that, rather than use of neat PLA, the use of its TPU or TPE blends would be still advantageous for both "indoor use" and also for "outdoor use." (c) 2018 Wiley Periodicals, Inc

Influence of rubber content on mechanical, thermal, and morphological behavior of natural rubber toughened poly(lactic acid)-multiwalled carbon nanotube nanocomposites

The effects of natural rubber (NR) on the mechanical, thermal, and morphological properties of multiwalled carbon nanotube (CNT) reinforced poly(lactic acid) (PLA) nanocomposites prepared by melt blending were investigated. A PLA/NR blend and PLA/CNT nanocomposites were also produced for comparison. The tensile strength and Youngs modulus of PLA/CNT nanocomposites improved significantly, whereas the impact strength decreased compared to neat PLA. The incorporation of NR into PLA/CNT significantly improved the impact strength and elongation at break of the nanocomposites, which showed approximately 200 and 850 increases at 20 wt NR, respectively. However, the tensile strength and Youngs modulus of PLA/NR/CNT nanocomposites decreased compared to PLA/CNT nanocomposites. The morphology analysis showed the homogeneous dispersion of NR particles in PLA/NR/CNT nanocomposites, while CNTs preferentially reside in the NR phase rather than the PLA matrix. In addition, the incorporation of NR into PLA/CNT lowered the thermal stability and glass-transition temperature of the nanocomposites