Study of thermal decomposition kinetics for polyimides based on 2,6-bis(4-aminophenyl)-4-(4-(4-aminophenoxy) phenyl) pyridine

被引:1
|
作者
Zhuo, Longhai [1 ,2 ]
Kou, Kaichang [1 ,2 ]
Bai, Yang [3 ]
Wang, Yiqun [1 ,2 ]
Wu, Guanglei [4 ]
机构
[1] Northwestern Polytech Univ, Sch Sci, Key Lab Space Appl Phys & Chem, Minist Educ, Xian 710129, Peoples R China
[2] Northwestern Polytech Univ, Sch Sci, Shaanxi Key Lab Macromol Sci & Technol, Xian 710129, Peoples R China
[3] Xian Modern Chem Res Inst, Xian, Peoples R China
[4] Xi An Jiao Tong Univ, Sch Elect Engn, CNRE, State Key Lab Elect Insulat & Power Equipment, Xian 710049, Peoples R China
基金
中国国家自然科学基金;
关键词
Polyimide; phthalimide pendant; terminate; hyperbranched; thermal decomposition kinetics; HYPERBRANCHED AROMATIC POLYIMIDES; DIANHYDRIDE; MECHANISM; MEMBRANES; TRIAMINE;
D O I
10.1177/0954008315583705
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This study reports on the preparation and thermal decomposition kinetics of a polyimide (PI) with phthalimide pendant (PI-1) and an analogous hyperbranched PI (PI-2). PI-1 was synthesized from 2,6-bis(4-aminophenyl)-4-(4-(4-aminophenoxy) phenyl) pyridine (BAAP) and 4,4'-(hexa-fluoroisopropylidene) diphthalic anhydride using a simple method with BAAP terminated by phthalic anhydride. The morphology of the PI structures was examined using X-ray diffraction. The thermal decomposition processes of the PIs were then studied according to a two-stage method using thermogravimetric analysis. The results indicated that both PIs exhibited excellent thermal stability, with a decomposition pattern of 5% mass loss beyond 508 degrees C and 10% beyond 529 degrees C. The two PIs exhibited similar levels of thermal stability in the first decomposition stage, but PI-1 exhibited higher stability in the second stage. The results indicate that PIs into which phthalimide pendants have been introduced retain their thermal stability in the first stage of decomposition and demonstrate enhanced thermal stability in the second stage.
引用
收藏
页码:390 / 400
页数:11
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