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This work investigated the thermal, morphological, and tensile properties of poly(l-lactide)-b-poly(ethylene glycol)-b-poly(l-lactide) (PLLA-PEG-PLLA)/thermoplastic starch (TPS) blends with 3 wt% citric acid (CA) treatment of TPS. The blends with PLLA-PEG-PLLA/CA-TPS ratios of 100/0, 90/10, 80/20, and 60/40 (w/w) were investigated and compared with PLLA-PEG-PLLA/CA-free TPS blends. Crystallizability of the blends decreased and thermal stability increased as the TPS content increased. The thermal stability of the blends was found to improve after CA treatment of TPS. The PLLA-PEG-PLLA/CA-TPS blends showed better phase compatibility than those of the PLLA-PEG-PLLA/CA-free TPS blends. The tensile properties of the blends were improved by CA treatment of TPS. In conclusion, improvement in thermal stability, phase compatibility, and tensile properties of the PLLA-PEG-PLLA/TPS blends was obtained by CA treatment of TPS. The resulting PLLA-PEG-PLLA/CA-TPS blends could potentially be used to prepare biodegradable and flexible bioplastics.

In this study, talcum was melt-blended with a flexible poly(l-lactide)-b-polyethylene glycol-b-poly(l-lactide) triblock copolymer (PLLA-PEG-PLLA) with 1, 2, 4, and 8 wt% talcum, for improvement of the crystallization and thermomechanical properties of PLLA-PEG-PLLA compared with PLLA. The crystallizability of PLLA-PEG-PLLA/talcum composites was better than that of PLLA/talcum composites as determined from differential scanning calorimetry. X-ray diffractometry showed that the PLLA-PEG-PLLA/talcum films had a higher degree of crystallinity than the PLLA/talcum films. PEG middle-blocks and talcum showed a synergistic effect for crystallization of PLLA end-blocks. The PLLA-PEG-PLLA/talcum films showed better thermomechanical properties than those of the PLLA/talcum films as determined from dynamic mechanical analysis. This was confirmed from the results of dimensional stability to heat. In summary, the PLLA-PEG-PLLA/talcum composites have potential for use as flexible bioplastics with good dimensional stability to heat.

Polymer blends of poly(L-lactide)-b-poly(ethylene glycol)-b-poly(L-lactide) (PLLA-PEG-PLLA) and high-density polyethylene (HDPE) with different blend ratios were prepared by a melt blending method. The thermal, morphological, mechanical, opacity, and biodegradation properties of the PLLA-PEG-PLLA/HDPE blends were investigated and compared to the PLLA/HDPE blends. The blending of HDPE improved the crystallization ability and thermal stability of the PLLA-PEG-PLLA; however, these properties were not improved for the PLLA. The morphology of the blended films showed that the PLLA-PEG-PLLA/HDPE blends had smaller dispersed phases compared to the PLLA/HDPE blends. The PLLA-PEG-PLLA/HDPE blends exhibited higher flexibility, lower opacity, and faster biodegradation and bioerosion in soil than the PLLA/HDPE blends. Therefore, these PLLA-PEG-PLLA/HDPE blends have a good potential for use as flexible and partially biodegradable materials. [ABSTRACT FROM AUTHOR]

High-molecular-weight poly( L -lactide) (HMW-PLLA) is a promising candidate for use as a bioplastic because of its biodegradability and compostability. However, the applications of HMW-PLLA have been limited due to its poor crystallizability. In this work, stereocomplex polylactide (scPLA) powder was prepared by precipitation of a low-molecular-weight poly( L -lactide)/poly( D -lactide) (LMW-PLLA/LMW-PDLA) blend solution and investigated for use as a fully-biodegradable nucleating agent for HMW-PLLA compared to LMW-PLLA powder. The obtained LMW-PLLA and scPLA powders with a nearly spherical shape showed complete homo- and stereocomplex crystallites, respectively. HMW-PLLA/LMW-PLLA powder and HMW-PLLA/scPLA powder blends were prepared by melt blending. The LMW-PLLA powder was homogeneously melted in the HMW-PLLA matrices, whereas the scPLA powder had good phase compatibility and was well-dispersed in the HMW-PLLA matrices, as detected by scanning electron microscopy (SEM). It was shown that the enthalpies of crystallization (Δ H c ) upon cooling scans for HMW-PLLA largely increased and the half crystallization time ( t 1/2 ) dramatically decreased as the scPLA powder content increased; however, the LMW-PLLA powder did not exhibit the same behavior, as determined by differential scanning calorimetry (DSC). The crystallinity content of the HMW-PLLA/scPLA powder blends significantly increased as the scPLA powder content increased, as determined by DSC and X-ray diffractometry (XRD). In conclusion, the fully biodegradable scPLA powder showed good potential for use as an effective nucleating agent to improve the crystallization properties of the HMW-PLLA bioplastic.

A poly( ε -caprolactone- co -L-lactide) copolyester was synthesized and employed to toughen poly(L-lactide) (PLLA) by reactive melt blending in the presence of an epoxy-based chain extender. The effects of chain extension reaction and copolyester content on properties of PLLA-based blends were studied. The chain extension reaction reduced crystallinity and melt flow index of PLLA/copolyester blends. Meanwhile the copolyester blending improved the crystallinities of the chain-extended PLLA up to 20 wt% copolyester. The phase compatibility between PLLA matrix and dispersed copolyester phases was enhanced by the chain extension reaction. The impact strength of chain-extended PLLA increased with the contents of copolyester and chain extender.