首页 | 本学科首页   官方微博 | 高级检索  
     

可生物降解聚酯P(ES-co-DGA)和P(BS-co-DGA)的合成及性能比较
引用本文:张敏,惠媛媛,李成涛,邱建辉. 可生物降解聚酯P(ES-co-DGA)和P(BS-co-DGA)的合成及性能比较[J]. 塑料科技, 2011, 39(12)
作者姓名:张敏  惠媛媛  李成涛  邱建辉
作者单位:1. 陕西科技大学教育部轻化工助剂化学与技术重点实验室,陕西西安,710021
2. 日本秋田县立大学,日本秋田015-0055
基金项目:陕西省教育厅产业化培育项目(2010JC01); 咸阳市科技计划项目(TD10-01)
摘    要:通过改变二乙醇酸(DGA)的含量,将其与乙二醇、1,4-丁二醇进行缩聚反应,得到了P(ES-co-DGA)和P(BS-co-DGA)共聚物,采用1H-NMR表征化学结构,并对共聚物的相对分子质量(Mn)、热性能、力学性能、降解性等进行比较研究。结果表明:随着DGA的增加,两种共聚物的熔点(Tm)均呈下降趋势,但P(ES-co-DGA)的玻璃化转变温度(Tg)逐渐升高,P(BS-co-DGA)的Tg却变化不大;所有共聚物的热分解温度(Td)(失重2%)均在300℃左右。当DGA含量为50%时,P(BS-co-DGA)的最大断裂伸长率可达到921%;当DGA含量为20%时,P(ES-co-DGA)的最大断裂伸长率可达到853%。随着DGA的增加,P(BS-co-DGA)的降解速率增大;当DGA含量为10%以上时,P(BS-co-DGA)的降解性能逐渐降低。

关 键 词:聚丁二酸乙二醇酯  聚丁二酸丁二醇酯  共聚改性  热稳定性  降解性

Synthesis and Performance Comparison of Biodegradable Polyesters of P(ES-co-DGA) and P(BS-co-DGA)
Zhang Min,Hui Yuanyuan,Li Chengtao,Qiu Jianhui. Synthesis and Performance Comparison of Biodegradable Polyesters of P(ES-co-DGA) and P(BS-co-DGA)[J]. Plastics Science and Technology, 2011, 39(12)
Authors:Zhang Min  Hui Yuanyuan  Li Chengtao  Qiu Jianhui
Affiliation:Zhang Min1,Hui Yuanyuan1,Li Chengtao1,Qiu Jianhui2 1 Key laboratory of Auxiliary Chemistry & Technology for Chemical Industry,Ministry of Education,Shaanxi University of Science & Technology,Xi'an 710021,China 2 Akita Prefecture University,Akita 015-0055,Japan
Abstract:The binary copolymers of P(ES-co-DGA) and P(BS-co-DGA) were synthesized by taking different contents of glycolic acid(DGA) through polycondensation with ethylene glycol and 1,4-butanediol.Chemical structures of the copolymers were characterized by 1H-NMR,and molecular weight,thermal properties,mechanical performance and degradations were also investigated and compared.The results show that with the increasing of DGA,the melting points(Tm) of these two copolymers decrease;the glass transition temperature(Tg)...
Keywords:Poly(ethylene-succinate)(PES)  Poly(butylene-succinate)(PBS)  Copolymerization modif ication  Thermal stability  Degradation  
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号