# Modification of Polylactide with Triblock and Diblock Copolymers of Ethylene Glycol and Propylene Glycol

## TL;DR

This paper explores how adding specific copolymers improves the mechanical properties of polylactide, especially elongation and impact strength.

## Contribution

The study introduces new triblock and diblock copolymers that significantly enhance polylactide's mechanical performance.

## Key findings

- Amorphous blends with triblock copolymer showed a 70-fold increase in elongation at break compared to pure PLA.
- Diblock copolymer blends exhibited higher tensile impact strength than neat PLA.
- Crystallized blends had elongation at break exceeding 7–25 times that of neat crystalline PLA.

## Abstract

Polylactide (PLA) was melt blended with block copolymers of ethylene glycol and propylene glycol: a triblock copolymer (PPG-b-PEG-b-PPG) with a molar mass of 2700 g/mol and 40 wt% PEG content, and a diblock copolymer (PPG-b-PEG) with a molar mass of 4000 g/mol and 50 wt% PEG content. The structure as well as the thermal and mechanical properties of both amorphous and crystallized blends were investigated. Due to the copolymers’ chemical composition and the resulting phase structure, the 10 wt% amorphous blends with PPG-b-PEG-b-PPG and PPG-b-PEG, with Tg values of 38 °C and 46 °C, respectively, exhibited relatively high yield stress, close to 45 MPa, along with remarkable elongation at break. Notably, the blend with the triblock copolymer showed a 70-fold increase in elongation at break compared to neat amorphous PLA. Furthermore, the tensile impact strength of the blend with the diblock copolymer surpassed that of neat PLA. Upon crystallization, the 10 wt% blends showed reduced yield stress and elongation at break; however, the elongation at break exceeded 7–25 times that of neat crystalline PLA. Furthermore, their tensile impact strength increased to more than three times the value of crystalline PLA.