Biodegradable polymer blends of poly(lactic acid) and poly(ethylene glycol)

TLDR

The PLA/PEG films were produced by melt‑blending and extrusion at ratios ranging from 100/0 to 30/70. PLA/PEG blends transition from miscible to partially miscible with increasing PEG, where PEG plasticizes PLA below 50 % to raise elongation and lower modulus, while above 50 % PEG crystallinity increases modulus and reduces elongation; tensile strength decreases linearly with PEG, and enzymatic degradation yields greater weight loss than pure PLA, with PLA‑driven loss below 30 % PEG and PEG dissolution dominating above 30 %. © 1997 John Wiley & Sons, Inc., J Appl Polym Sci 66:1495–1505.

Abstract

Poly(lactic acid) (PLA) and poly(ethylene glycol) (PEG) were melt-blended and extruded into films in the PLA/PEG ratios of 100/0, 90/10, 70/30, 50/50, and 30/70. It was concluded from the differential scanning calorimetry and dynamic mechanical analysis results that PLA/PEG blends range from miscible to partially miscible, depending on the concentration. Below 50% PEG content the PEG plasticized the PLA, yielding higher elongations and lower modulus values. Above 50% PEG content the blend morphology was driven by the increasing crystallinity of PEG, resulting in an increase in modulus and a corresponding decrease in elongation at break. The tensile strength was found to decrease in a linear fashion with increasing PEG content. Results obtained from enzymatic degradation show that the weight loss for all of the blends was significantly greater than that for the pure PLA. When the PEG content was 30% or lower, weight loss was found to be primarily due to enzymatic degradation of the PLA. Above 30% PEG content, the weight loss was found to be mainly due to the dissolution of PEG. During hydrolytic degradation, for PLA/PEG blends up to 30% PEG, weight loss occurs as a combination of degradation of PLA and dissolution of PEG. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 66: 1495–1505, 1997