TY - JOUR
T1 - Synthesis, characterization and properties of poly(butanediol sebacate–butanediol terephthalate) (PBSeT) copolyesters using glycerol as cross-linking agent
AU - Li, Zhimao
AU - Li, Yingchun
AU - Dong, Xing
AU - Wang, Wensheng
AU - Zhu, Yong Chuang
AU - Murugadoss, Vignesh
AU - Song, Gang
AU - Naik, Nithesh
AU - Pan, Duo
AU - Guo, Zhanhu
N1 - Funding Information:
The authors thank Maoyong He of Taiyuan Institute of Technology for his help.
Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2021/9
Y1 - 2021/9
N2 - High molecular weight aliphatic-aromatic copolyesters were synthesized from Sebacic acid, terephthalic acid, 1, 4-butanediol and glycerol via two-step esterification and polycondensation. Copolyesters were characterized with intrinsic viscosity, gel permeation chromatography, X-ray diffraction, Fourier infrared spectroscopy, nuclear magnetic resonance, differential scanning calorimetry, thermogravimetric analysis, rheological analysis, tensile and puncture testing. All the copolyesters had a weight-average molecular weight over 20,000 g/mol or intrinsic viscosity over 1.1 dL/g when the glycerol content was in the range from 0.04 to 0.1 mol. Particularly, in addition to a small reduction in the tensile strength and elongation at break, the molecular weight, crystallinity, and intrinsic viscosity of the polyester were increased when the glycerol content was 0.04 mol, and the puncture resistance reached its maximum, which would improve the performance of the copolyester film. Obviously, the addition of glycerol did not significantly affect the melting temperature, glass transition temperature and thermal stability of polyesters, which would make it possible to use copolyester as a base material for cold-resistant hydrogels. As a whole, the level of glycerol within 0.1 mol is sufficient to improve the properties of copolyesters, which is beneficial to promote the generalization of them for films and hydrogels.
AB - High molecular weight aliphatic-aromatic copolyesters were synthesized from Sebacic acid, terephthalic acid, 1, 4-butanediol and glycerol via two-step esterification and polycondensation. Copolyesters were characterized with intrinsic viscosity, gel permeation chromatography, X-ray diffraction, Fourier infrared spectroscopy, nuclear magnetic resonance, differential scanning calorimetry, thermogravimetric analysis, rheological analysis, tensile and puncture testing. All the copolyesters had a weight-average molecular weight over 20,000 g/mol or intrinsic viscosity over 1.1 dL/g when the glycerol content was in the range from 0.04 to 0.1 mol. Particularly, in addition to a small reduction in the tensile strength and elongation at break, the molecular weight, crystallinity, and intrinsic viscosity of the polyester were increased when the glycerol content was 0.04 mol, and the puncture resistance reached its maximum, which would improve the performance of the copolyester film. Obviously, the addition of glycerol did not significantly affect the melting temperature, glass transition temperature and thermal stability of polyesters, which would make it possible to use copolyester as a base material for cold-resistant hydrogels. As a whole, the level of glycerol within 0.1 mol is sufficient to improve the properties of copolyesters, which is beneficial to promote the generalization of them for films and hydrogels.
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U2 - 10.1016/j.mtcomm.2021.102557
DO - 10.1016/j.mtcomm.2021.102557
M3 - Article
AN - SCOPUS:85108888245
SN - 2352-4928
VL - 28
JO - Materials Today Communications
JF - Materials Today Communications
M1 - 102557
ER -