Sequence Distribution, Thermal Properties, and Crystallization Studies of Poly(trimethylene terephthalate-co-1,4-cyclohexylene dimethylene terephthalate) Copolyesters

被引:9
|
作者
Yang, Jian [1 ]
Li, Wengang [2 ]
Yu, Aifang [2 ]
Xi, Peng [2 ]
Huang, Xiang'an [2 ]
Li, Suming [1 ,3 ]
机构
[1] Fudan Univ, Dept Mat Sci, Shanghai 200443, Peoples R China
[2] Donghua Univ, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 200051, Peoples R China
[3] Univ Montpellier I, Max Mousseron Inst Biomol, F-34060 Montpellier, France
关键词
polyester; thermal properties; crystallization; COCRYSTALLIZATION BEHAVIOR; CRYSTAL-STRUCTURE; POLY(BUTYLENE TEREPHTHALATE)S; CYCLOHEXYL;
D O I
10.1002/app.29340
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A series of novel poly(trimethylene terephthalate-co-1,4-cyclohexylene dimethylene terephthalate) (PTCT) with various compositions were synthesized by melt polycondensation of 1,3-propanediol, 1,4-cyclohexane-dimethanol and dimethyl terephthalate. The resulting copolyesters were characterized using C-13 and H-1 nuclear magnetic resonance. The average length of both trimethylene terephthalate (TT) and cyclohexylene dimethylene terephthalate (CT) sequences varies from 1 to 10, and the chain structure is statistically random. The crystallization was investigated using wide angle X-ray diffractometer (WAXD) and differential scanning calorimeter. The WAXD patterns can be divided in two groups according to the compostion: copolyesters with less than 35 mol % CT content exhibit PTT-type lattice, and those with CT unit content higher than 42 mol % cyrstallize with the PCT-type lattice. The crystallization of CT sequence is higher than that of TT sequence. Thermodynamic analysis shows that the comonomer is excluded from the PTT-type or PCT-type crystal of the copolyesters. The thermal decomposition temperature of copolyesters increases with increasing CT content, and their thermal stability is improved as compared to that of PTT. (C) 2008 Wiley Periodicals, Inc. J Appl Polym Sci 111: 2751-2760, 2009
引用
收藏
页码:2751 / 2760
页数:10
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