甘油
增塑剂
热塑性塑料
淀粉
丁二醇
结晶度
低聚物
材料科学
高分子化学
单体
己二酸
化学
化学工程
聚合物
有机化学
复合材料
发酵
工程类
作者
Haishun Ouyang,Dongliang Jin,Ya‐Ling He,Kewen Tang,Xiaoming Guo,Lin Ye,Fei Cheng,Ping Zhu,Dongfang Wu,Kang Zhang
标识
DOI:10.1016/j.ijbiomac.2024.131603
摘要
The thermoplastic starch with glycerol is easy to retrograde and sensitive to hygroscopicity. In this study, branched 1,4-butanediol citrate oligomers with different molecular weights (P1, P2, and P3) are synthesized, and then mixed with glycerol (G) as the co-plasticizers to prepare thermoplastic starch (CS/PG). The results show that the molecular weight and branching degree of the branched 1,4-butanediol citrate oligomers increase as reaction time prolongs. Compared with glycerol plasticized starch, the thermoplastic starch films with branched 1,4-butanediol citrate oligomers/glycerol (10 wt%/20 wt%) have a better toughness, transmittance, and aging resistance, and have a lower crystallinity, hygroscopicity, and thermal stability. The toughness, transmittance, and aging resistance of CS/PG films are positively correlated with the molecular weight of the branched 1,4-butanediol citrate oligomers. These are due to the fact that the branched 1,4-butanediol citrate oligomer with a high molecular weight could form a stronger hydrogen bond and the more stable cross-linked structure with starch chains than that with a lower molecular weight. The elongation at break of CS/P3G film stored for 3 and 30 d are 98.0 % and 88.1 %, respectively. The mixture of branched butanediol citrate oligomers and glycerol, especially P3/G, has a potential application in the preparation of thermoplastic starch.
科研通智能强力驱动
Strongly Powered by AbleSci AI