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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Biobased copolyesters from renewable resources: synthesis and crystallization behavior of poly(decamethylene sebacate-co-isosorbide sebacate)

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论文类型:期刊论文

发表时间:2015-01-01

发表刊物:RSC ADVANCES

收录刊物:SCIE、EI、Scopus

卷号:5

期号:53

页面范围:42777-42788

ISSN号:2046-2069

摘要:A series of long chain aliphatic copolyesters poly(decamethylene sebacate-co-isosorbide sebacate) (P(DS-co- IS)) were synthesized from commercially available biobased sebacic acid (SA), 1,10-decanediol (DD) and isosorbide (ISB) through a two-step melt polycondensation method. The molecular weight, composition, and microstructure of the P(DS-co-IS) copolyesters were characterized by GPC, H-1-NMR, and C-13-NMR. The crystallization properties of the P(DS-co-IS) copolyesters were depressed, while the glass transition temperature was enhanced by the incorporation of isosorbide with a bulky rigid structure. The nonisothermal melt crystallization peak temperature and melting point decreased for P(DS-co-IS) with increasing the number of ISB unit; moreover, the equilibrium melting point temperature of P(DS-co-IS) was also reduced. However, the introduction of the ISB segment did not change the crystal structure of P(DS-co-IS), but it gradually decreases the crystallinity. Isothermal crystallization kinetics of neat PDS and its copolyesters indicated that PDS possesses high crystallization ability, which is a characteristic of long chain aliphatic polyesters. The crystallization mechanism remains unchanged for both neat PDS and P(DS-co-IS); however, the crystallization rates of P(DS-co-IS) decreased with increasing ISB composition and crystallization temperature. No evidence of ring-banded spherulites could be detected for this long chain PDS and its copolyesters in a wide temperature range even when supercooled.