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Synthesis and thermal decomposition of GAP-Poly(BAMO) copolymer

机译:GAP-Poly(BAMO)共聚物的合成与热分解

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摘要

An energetic copolymer of glycidyl azide polymer (GAP) and poly(bis(azidomethyl)oxetane (Poly(BAMO)) was synthesized using the Borontrifluoride—dimethyl ether complex/diol initiator system. The synthesized copolymer exhibited the characteristics of an energetic thermoplastic elastomer (ETPE). Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) were used to study the thermal decomposition behavior and the results were compared with that of the constituent homopolymers. The main weight loss step in all the polymers coincides with the exothermic dissociation of the azido groups in the side chain. In contrast with the behavior of the homopolymers, the copolymer shows a broad exothermic shoulder peak at 298℃ after the main exothermic decomposition peak at 228℃. Kinetic analysis was performed by Vyazovkin's model-free method, which suggests that the activation energy of the main decomposition step is around 145 kJ/mol and for the second shoulder it is around 220 kJ/mol. Fourier transform infra red (FTIR) spectra of the degradation residues show that the azido groups in the copolymer decompose in two stages at different temperatures which is responsible for the double decomposition behavior.
机译:利用三氟化硼-二甲醚配合物/二醇引发剂体系合成了缩水甘油叠氮化物聚合物(GAP)和聚(双(叠氮甲基)氧杂环丁烷(Poly(BAMO)))的高能共聚物,该共聚物表现出高能热塑性弹性体的特性(用热重分析(TGA)和差示扫描量热法(DSC)研究热分解行为,并将结果与​​组成均聚物的热分解行为进行比较,所有聚合物的主要失重步骤都与聚合物的放热解离相符。与均聚物的行为相反,该共聚物在228℃的主要放热分解峰之后,在298℃显示一个宽的放热肩峰,并通过Vyazovkin的无模型方法进行了动力学分析。表明主要分解步骤的活化能约为145 kJ / mol,而第二个肩峰的活化能约为220 kJ / m哦降解残基的傅立叶变换红外(FTIR)光谱表明,共聚物中的叠氮基在不同温度下分两个阶段分解,这是造成双分解行为的原因。

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