膜
热稳定性
化学
丙烷
玻璃化转变
部分
高分子化学
二胺
对苯二甲酰氯
有机化学
聚合物
缩聚物
生物化学
作者
Blanca Díez,Purificación Cuadrado,Ángel Marcos‐Fernández,José G. de la Campa,Alberto Tena,Pedro Prádanos,Laura Palacio,Young Moo Lee,Cristina Álvarez,Ángel E. Lozano,A. Hernández
标识
DOI:10.1016/j.reactfunctpolym.2018.03.013
摘要
Two series of aromatic poly(ortho-hydroxyamide)s (poly(o-hydroxyamide)s, HPAs) were prepared by reaction of two diamines, 2,2-bis(3-amino-4-hydroxyphenyl) propane (APA) and 2,2-bis(3-amino-4-hydroxyphenyl) hexafluoropropane (APAF), with four aromatic diacid chlorides; terephthaloyl dichloride (TPC), isophthaloyl dichloride (IPC), 2,2-bis[4-chlorocarbonylphenyl)hexafluoropropane (6FC) and 4,4′-sulfonyldibenzoyl dichloride (DBSC). Amorphous HPAs with high molecular weights (inherent viscosities higher than 0.5 dL/g) and relatively high glass transition temperatures (220–280 °C) were obtained. Dense membranes of HPAs were able to undergo a thermal rearrangement (TR) process to polybenzoxazoles (β-TR-PBOs) heating at moderate temperatures (between 250 and 375 °C), and their complete conversion was reached at a temperature below 375 °C, depending on the o-hydroxy diamine moiety, APA and APAF. The β-TR-PBOs films derived from APAF showed a higher thermal stability and higher Tg than those from APA. Gas separation properties of TR-PBOs membranes were superior to those of their poly(o-hydroxyamide) precursors, particularly for the following gas pairs: O2/N2, CO2/CH4, He/CH4 and He/CO2.
科研通智能强力驱动
Strongly Powered by AbleSci AI