首页> 外文期刊>Thermochimica Acta: An International Journal Concerned with the Broader Aspects of Thermochemistry and Its Applications to Chemical Problems >Synthesis, curing kinetics and thermal properties of a novel self-promoted fluorene-based bisphthalonitrile monomer
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Synthesis, curing kinetics and thermal properties of a novel self-promoted fluorene-based bisphthalonitrile monomer

机译:新型的自促进芴基双邻苯二甲腈单体的合成,固化动力学和热性能

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摘要

A novel amino-containing fluorene-based bisphthalonitrile monomer, 9,9-bis(4-aminophenyl)-2,7-(3,4-dicyanophenoxy)-fluorene (AFPN), was successfully synthesized via the nucleophilic displacement of the nitro-substituent from 4-nitrophthalonitrile. The structure of AFPN was confirmed by Fourier transform infrared (FT-IR), H-1 and C-13 nuclear magnetic resonance (NMR). Its curing behavior and curing kinetics were investigated using differential scanning calorimetry (DSC) and FT-IR techniques. Isoconversional method based on Starink was applied to analyze the curing process of AFPN. The thermal and mechanical properties of the cured product were evaluated by thermogravimetric analysis (TGA) and dynamic mechanical analysis (DMA). The AFPN showed a self-promoted curing behavior, whereas the introduction of the amino groups increased its curing rate and lowered its curing temperature. Additionally, its cured polymer showed an excellent thermal and thermo-oxidative stability, since its char yield reached 76.5% at 800 degrees C in nitrogen and 83.4% at 600 degrees C in air, respectively. (C) 2015 Elsevier B.V. All rights reserved.
机译:通过硝基的亲核取代成功地合成了一种新型的含氨基芴基双邻苯二甲腈单体9,9-双(4-氨基苯基)-2,7-(3,4-二氰基苯氧基)-芴(AFPN)。 4-硝基邻苯二甲腈的取代基。 AFPN的结构通过傅立叶变换红外(FT-IR),H-1和C-13核磁共振(NMR)得以确认。使用差示扫描量热法(DSC)和FT-IR技术研究了其固化行为和固化动力学。采用基于Starink的等转化法分析了AFPN的固化过程。固化产物的热和机械性能通过热重分析(TGA)和动态力学分析(DMA)进行评估。 AFPN表现出自我促进的固化行为,而氨基的引入提高了其固化速率并降低了固化温度。另外,其固化的聚合物表现出优异的热和热氧化稳定性,这是因为其炭含量在800摄氏度的氮气中分别达到76.5%和600摄氏度的空气中达到83.4%。 (C)2015 Elsevier B.V.保留所有权利。

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