Chain heterogeneity of poly(lactic acid) and its influence on crystallization kinetics

被引:0
|
作者
Yang, Tao [1 ]
He, Shuang [1 ]
Liu, Peng [1 ]
Yan, Jingyao [1 ]
Lu, Ruiyao [1 ]
Xue, Yanhu [1 ,2 ]
机构
[1] Tianjin Univ Sci & Technol, Coll Chem Engn & Mat Sci, Tianjin 300457, Peoples R China
[2] Tsinghua Univ, Dept Chem Engn, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Poly(lactic acid); Temperature rising elution fractionation; Chain microstructure; RISING ELUTION FRACTIONATION; COLD CRYSTALLIZATION; L-LACTIDE; COPOLYMERS; MELT; POLYMERIZATION; NMR;
D O I
10.1016/j.ijbiomac.2024.134101
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Temperature rising elution fractionation (TREF) approach was used to separate a biodegradable poly(lactic acid) (PLA) resin into ten fractions and completely establish the relationship between chain microstructure and properties. The main fractions were mainly eluted at 100, 110, 114, and 118 degrees C, and their mass percentages were 7.98 wt%, 44.83 wt%, 19.64 wt%, and 11.90 wt%, respectively. Through the use of successive self-nucleation/ annealing (SSA) thermal fractionation, gel permeation chromatography (GPC), differential scanning calorimetry (DSC), and 13C-nuclear magnetic resonance spectroscopy (13C NMR), the intermolecular and intramolecular differences of PLA were further explored. Fractions eluted at 90, 110, 118, and 126 degrees C were also chosen to research the non-isothermal cold crystallization kinetics, and fractions eluted at 110, 118, and 126 degrees C were chosen to explore the non-isothermal crystallization kinetics in order to simulate the real process. The findings demonstrated that the Liu-Mo approach were more suited the non-isothermal crystallization and non-isothermal cold crystallization kinetics of PLA. As the elution temperature increased, so did the stereoregularity of the fractions, the crystallization rate, the crystallization capacity, and the lamellar thickness. These will lay a foundation for its basic research and industrial application.
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页数:13
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