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Fluorinated Polybenzimidazopyrrolones with Excellent Alkaline-Hydrolysis Resistance

机译:耐碱性水解性优异的氟化聚苯并咪唑并吡咯烷酮

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摘要

Two novel aromatic tetraamines containing bulky lateral phenyl unit and multiple trifluoromethyl groups, 1,1-bis[4-(3',4'-diaminophenoxy)phenyl]-1-(3"-trifluoromethylphenyl)22,2,2-trifluoroethane (6FTA) and 1,1-bis[4-(3',4'-diaminophenoxy)phenyl]-1-[3",5"-bis(trifluoromethyl)phenyl]-2,2,2-trifluoroethane (9FTA) were synthesized and characterized. A series of fluorinated aromatic polybenzimidazopyrrolones (polypyrrolones, PPys) were synthesized via a two-step polycondensation procedure. The inherent viscosities of the precursors, poly(amide amino acid) (PAAA), ranged from 0.39 dL/g to 0.54 dL/g. All the FPPys were amorphous. The freestanding FPPy films could be prepared, which exhibited good thermal stability with the glass transition temperature of 315-389℃, the temperatures of 5% weight loss (T5%) of 497-535℃ in nitrogen and residual weight retention at 700℃ over 60%. All the FPPy films exhibited excellent alkaline-hydrolysis resistance which retained their original shapes and toughness after boiling 7 days in 10% sodium hydroxide solution. Also after boiling 8 h in 10% sodium hydroxide solution, the tensile strength could retain as high as 56% of the original values. The alkaline-hydrolysis resistance was much better than the polyimides which had similar chemical structures.
机译:两种新颖的芳香四胺,均含有庞大的侧向苯基单元和多个三氟甲基,即1,1-双[4-(3',4'-二氨基苯氧基)苯基] -1-(3“-三氟甲基苯基)22,2,2-三氟乙烷( 6FTA)和1,1-双[4-(3',4'-二氨基苯氧基)苯基] -1- [3“,5”-双(三氟甲基)苯基] -2,2,2-三氟乙烷(9FTA)通过两步缩聚反应合成了一系列氟化芳族聚苯并咪唑并吡咯烷酮(聚吡咯烷酮,PPys),其前体的固有粘度(酰胺氨基酸)(PAAA)的粘度为0.39 dL / g至0.54。 dL / g。所有的FPPys均为无定形,可以制备独立的FPPy薄膜,具有良好的热稳定性,玻璃化温度为315-389℃,失重5%(T5%)为497-535℃ FPPy薄膜具有优异的耐碱性水解性,并保持了原有的形状和韧性在10%的氢氧化钠溶液中煮沸7天后,再加水。同样在10%的氢氧化钠溶液中沸腾8小时后,拉伸强度仍可保持高达原始值的56%。耐碱水解性比具有相似化学结构的聚酰亚胺要好得多。

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