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Developing Toughened Aromatic Polybenzoxazines Using Thermoplastic Oligomers and Telechelics, Part 1: Preparation and Characterization of the Functionalized Oligomers

机译:使用热塑性低聚物和远螯剂开发增韧的芳族聚苯并恶嗪,第1部分:功能化低聚物的制备和表征

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摘要

The preparation and characterization of three families of thermoplastic oligomers (M n 5 2918-13263 g mol~(-1)) based on polyarylsulfone (PSU) differing in both molecular weight and terminal functionality and one series of polyarylethersulfone (PES) of different molecular weights is reported. Infrared and nuclear magnetic resonance spectroscopy data support the formation of both the hydroxyl terminated oligomers and conversion (67-89% depending on molecular weight) to the telechelic PSU oligomer bearing reactive benzoxazine groups. Differential scanning calorimetry reveals that the onset of homopolymerization in the telechelic PSU oligomer occurs at around 100 ℃ (peak maximum 125 ℃ at 10 K/min) and rescans show values of the glass transition (for the homopolymers) ranging from 124 to 167 ℃ depending on molecular weight. The influence on the oligomer backbone and terminal functionality is examined using thermal analysis.
机译:基于分子量和末端官能度不同的聚芳基砜(PSU)和一系列不同分子的聚芳基醚砜(PES)的三族热塑性低聚物(M n 5 2918-13263 g mol〜(-1))的制备和表征报告重量。红外和核磁共振光谱数据支持羟基封端的低聚物的形成和转化(取决于分子量的67-89%)到带有反应性苯并恶嗪基团的远螯PSU低聚物的转化。差示扫描量热法表明,远螯PSU低聚物发生均聚反应的温度约为100℃(在10 K / min时,最大峰值温度为125℃),重新扫描后的玻璃化转变温度(对于均聚物)范围为124至167℃分子量。使用热分析检查了对低聚物主链和末端官能度的影响。

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