Synthesis of novel thermoplastic polyester elastomers with biobased amorphous polyester as the soft segment

被引:2
|
作者
Xu, Yanyan [1 ]
Zhang, Qinan [1 ,2 ]
Wang, Zhao [1 ,2 ]
Zhang, Liqun [1 ,2 ,3 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, Beijing Engn Res Ctr Adv Elastomers, Beijing 100029, Peoples R China
[3] South China Univ Technol, Dept Polymer Mat & Engn, Guangzhou 510640, Peoples R China
基金
中国国家自然科学基金;
关键词
Biobased; Thermoplastic; Polyester elastomers; Block copolymers; Copolymerization; MULTIBLOCK COPOLYMERS SYNTHESIS; 2,5-FURANDICARBOXYLIC ACID; MECHANICAL-PROPERTIES; ENZYMATIC-SYNTHESIS; BLOCK; COPOLYESTERS; CRYSTALLIZATION; SUCCINATE; BEHAVIOR;
D O I
10.1016/j.polymertesting.2023.108088
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The development of sustainable polymers from biobased blocks is urgently desirable. In this work, a class of novel biobased thermoplastic polyester elastomers, namely poly(butylene terephthalate)-poly(1,4-butylene/2,3-butylene succinate) (PBT-PBBS) copolyesters, were designed and synthesized via melt oligomer poly -condensation of common PBT oligomer and biobased PBBS oligomer. The obtained PBT-PBBS copolyesters exhibited desired block structure and contained a hard phase of crystallized PBT and a soft phase of amorphous PBBS. Their mechanical properties could be tailored by tuning the polycondensation time or the molar ratio of PBT to PBBS. Specifically, the tensile strength and the elongation at break of these copolyesters could be flexibly adjusted in the range of 6-13 MPa and 240-650%, respectively. Therefore, they are expected to be widely used in the fields of elastomers, hot-melt adhesives, and toughening modifiers.
引用
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页数:8
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