Effect of chain segment length on crystallization behaviors of poly(l-lactide-b-ethylene glycol-b-l-lactide) triblock copolymer. Issue 2 (February 2020)

• Record Type: Journal Article
• Authors: Gong, Yongji; Song, Weihua; Wu, Yifan; Zhang, Daohai; Liu, Yufei; Zhao, Qian; He, Min; Chen, Xiaolang
• Is Part Of: Polymers and polymer composites. Volume 28:Issue 2(2020)
• Page Start: 77
• Page End: 88
• Publication Date: 2020-02
• Subjects: PLLA -- triblock copolymers -- crystallization behavior -- morphology; Polymers -- Periodicals; 668.905
• DOI: 10.1177/0967391119863951
• Languages: English
• ISSNs: 0967-3911

Abstract

The poly(l -lactide-b-ethylene glycol-b-l -lactide) (PLLA-PEG-PLLA) triblock copolymers with different chain segment length are fabricated by ring-opening polymerization. The structure, molecular weight, and crystallization behaviors of the triblock copolymers are characterized by Fourier transform infrared, nuclear magnetic resonance spectroscopy, gel permeation in chromatography, X-ray diffraction, differential scanning calorimetry, and polarizing optical microscopy (POM). The results show that the increase of block length is beneficial to improve its crystallization. In addition, the triblock copolymer exhibits a double crystallization phenomenon. The POM results indicate that PEG and PLLA chains of the copolymer crystallize in their respective crystallization temperature regions. The growth rate of the PLLA spherocrystal decreases and the dendritic spherocrystals appear with increasing the PEG chain length when the PLLA chain of the copolymer is isothermal crystallized at 80°C and PLLA chain length is constant. The growth rate of the PEG spherocrystal decreases and the spherocrystal morphology changes little with increasing PLLA chain length when the PEG chain is isothermal crystallized at 25°C and the length of PEG chain remained unchanged.