Well-defined high molecular weight polyglycolide-b-poly(L-)lactide-b-polyglycolide triblock copolymers: synthesis, characterization and microstructural analysis

被引:13
作者
Ayyoob, Muhammad [1 ]
Lee, Seungmook [1 ]
Kim, Young Jun [1 ]
机构
[1] Sungkyunkwan Univ, Polymer Chem Lab, Dept Chem Engn, 2066 Seobu Ro, Suwon 16419, South Korea
关键词
Biodegradable; Biocompatible; Block copolymers; B-PLLGA; Polylactide; Polyglycolide; Ring-opening polymerization; POLY(LACTIC ACID); MECHANICAL-PROPERTIES; ALIPHATIC POLYESTERS; BLOCK-COPOLYMERS; L-LACTIDE; PLA; POLYCONDENSATION; GLYCOLIDE; SEQUENCE; HYDROLYSIS;
D O I
10.1007/s10965-019-2001-4
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Block copolymerization is already a proven technique to manipulate the properties of polymeric materials. Herein, our work presents a facile synthesis of high molecular weight polyglycolide-b-poly(L-)lactide-b-polyglycolide (b-PLLGA) triblock copolymers by ring-opening polymerization (ROP) in bulk at considerably low temperature. A series of ABA-type triblock copolymers was successfully prepared and microstructural properties were thoroughly investigated against random copolymers of poly(L-lactide-co-glycolide) (r-PLLGA). This synthesis method led to the preparation of high molecular weight b-PLLGAs with highly defined chain microstructure and an intrinsic viscosity [eta] was obtained as high as 1.62 dl/g when [M]:[I] was [1]:[1000]. The investigations revealed that the prepared copolymers are in block type chain microstructure, having exclusive thermal transitions and sequence/segment properties. DSC analysis revealed that two glass (T-g) transitions and two melt transitions (T-m) exclusively associated to PGA block and PLLA block. Results were further confirmed by homosequenses of -LLLL- and -GGGG- from C-13-NMR spectroscopy. Tensile results revealed that b-PLLGA have higher tensile strength and Young's modulus as compared to r-PLLGA. Moreover, b-PLLGAs are more thermally stable and have a wider thermal processing window.
引用
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页数:12
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