魏志勇

个人信息Personal Information

副教授

博士生导师

硕士生导师

主要任职:Null

性别:男

毕业院校:大连理工大学

学位:博士

所在单位:化工学院

学科:高分子材料. 高分子化学与物理

办公地点:西部校区化工实验楼A306

联系方式:13841142437

电子邮箱:zywei@dlut.edu.cn

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Effect of chain length of comonomeric diols on competition and miscibility of isodimorphism: A comparative study of poly(butylene glutarate-co-butylene azelate) and poly(octylene glutarate-co-octylene azelate)

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论文类型:期刊论文

发表时间:2018-08-01

发表刊物:EUROPEAN POLYMER JOURNAL

收录刊物:SCIE

卷号:105

页面范围:274-285

ISSN号:0014-3057

关键字:Isodimorphism; Even-odd copolyesters; Chain length effect

摘要:Two series of biobased even-odd aliphatic copolyesters, poly(butylene glutarate-co-butylene azelate) (PBGA) and poly(octylene glutarate-co-octylene azelate) (POGA), were prepared from even diol of 1,4-butanediol or 1,8-octanediol with odd diacids of glutaric acid and azelaic acid, respectively. These even-odd copolyesters can cocrystallize within the entire composition range despite being random, displaying a pseudo-eutectic point when their melting points are plotted as a function of composition. DSC and WAXD studies confirmed the isodimorphic behavior for PBGA and POGA. Then, the competition and miscibility in isodimorphism between PBGA and POGA were comparatively investigated. It demonstrated that the chain length of comonomeric diols can exert a considerable influence on the isodimorphic behavior of copolyesters. The comonomeric diol with longer chain shows greater ability in bridging the gap of competition between comonomer units. This insight contributes to predicting the composition of crystal transition point for isodimorphic copolyesters based on the molecular structure. For miscibility, the mutual insertion of comonomer units in the copolyester containing longer co-monomeric diol is easier than in the copolyester with shorter comonomeric diol. Furthermore, a close dependence between the mechanical properties with competition and miscibility in such even-odd copolyesters was observed and discussed. The composition dependence of yield stress presents a similar pseudo-eutectic behavior that matches those exhibited by T-m versus composition, and that of the elongation at break shows an opposite tendency. In conclusion, our work here not only clarifies the effect of chain length of comonomeric diols on competition and miscibility of isodimorphism in the even-odd copolyesters, but also provides guidance in the selection of comonomeric diol for preparation of aliphatic copolyesters with desirable performances.