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聚(乳酸)基三嵌段共聚物的合成、表征及结晶行为。

Synthesis, characterization, and crystallization behaviors of poly(-lactic acid)-based triblock copolymer.

机构信息

Key Laboratory of Advanced Materials Technology Ministry of Education, School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu, 610031, China.

Key Laboratory of Karst Environment and Geohazard, Ministry of Land and Resources, Guizhou University, Guiyang, 550025, China.

出版信息

Sci Rep. 2020 Feb 27;10(1):3627. doi: 10.1038/s41598-020-60458-9.

Abstract

Poly(-lactic acid) (PDLA) with different polyethylene glycol (PEG) segment synthesized PDLA-PEG-PDLA triblock copolymer through the ring-opening reaction of -LA and PEG will be used as a toughening modifier. The microstructure, crystal structures and crystallization behaviors of this triblock copolymer were investigated by Fourier transform infrared (FTIR) spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, X-ray diffraction (XRD), differential scanning calorimetry (DSC) and polarized optical microscopy (POM). The triblock copolymer is synthesized from the appearance of CH stretching vibration peak at 2910 cm and C-O stretching vibration peak at 1200 cm from PEG in FTIR spectra. Moreover, the chemical shift that is about 3.6 ppm in H NMR and 68.8ppm in C NMR proves this matter. The results of XRD and DSC reveal that PDLA and PEG are crystallized separately, and are not fully compatible, and microphase separation has occurred in this triblock copolymer. PEG can induce the triblock copolymer to accelerate the rate of crystallization, allowing it to crystallize more completely in the same amount of time. When the molecular weight of PEG is 6000 or the ratio of -LA/PEG is 1/1, the crystallizability of PDLA-PEG-PDLA triblock copolymer is the best.

摘要

聚(丙交酯)(PDLA)与不同的聚乙二醇(PEG)段通过 -LA 和 PEG 的开环反应合成 PDLA-PEG-PDLA 三嵌段共聚物,将用作增韧改性剂。通过傅里叶变换红外(FTIR)光谱、核磁共振(NMR)光谱、X 射线衍射(XRD)、差示扫描量热法(DSC)和偏光显微镜(POM)研究了这种三嵌段共聚物的微观结构、晶体结构和结晶行为。从 FTIR 光谱中 PEG 的 2910cm 处的 CH 伸缩振动峰和 1200cm 处的 C-O 伸缩振动峰的出现可以看出三嵌段共聚物的合成。此外,在 H NMR 中约 3.6 ppm 和 C NMR 中 68.8 ppm 的化学位移证明了这一点。XRD 和 DSC 的结果表明 PDLA 和 PEG 分别结晶,并且不完全相容,在这种三嵌段共聚物中发生了微相分离。PEG 可以诱导三嵌段共聚物加速结晶速率,使其在相同的时间内更完全地结晶。当 PEG 的分子量为 6000 或 -LA/PEG 的比例为 1/1 时,PDLA-PEG-PDLA 三嵌段共聚物的结晶性最佳。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e410/7046728/47c20fe3a3bf/41598_2020_60458_Fig1_HTML.jpg

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