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Copolymers based on GAP and 1,2-Epoxyhexane as Promising Prepolymers for Energetic Binder Systems

机译:基于间隙和1,2-环氧己烷的共聚物作为能量粘合剂系统有前途的预聚物

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Copolymers of epichlorohydrin (ECH) and 1,2-epoxyhexane (EpH) have been synthesized via cationic ring-opening polymerization using BF(3)xTHF as a catalyst. Structures of the resulting polymers have been confirmed by IR and NMR spectroscopy and GPC. In a subsequent reaction with NaN3 in DMSO, the halogenated precursors were completely azidated, which was confirmed by the same spectroscopic methods. The introduced pendant n-butyl chains act as an internal plasticizer by lowering the glass transition temperature (T-g) of the copolymers compared to the reference compound glycidyl azide polymer (GAP). Compared to GAP in a similar molecular weight range, the copolymers also showed reduced viscosity. These properties make the described copolymers interesting candidates for use as energetic binders in cast-cure applications.
机译:通过使用BF(3)XTHF作为催化剂,通过阳离子环开环聚合通过阳离子开环聚合合成了表氯醇(ECH)和1,2-环氧己烷(EPH)的共聚物。 通过IR和NMR光谱和GPC证实所得聚合物的结构。 在随后与DMSO中的NaN 3反应中,完全叠加卤代前体,通过相同的光谱方法证实。 通过将共聚物的玻璃化转变温度(T-G)与参考化合物氧化乙胺(间隙)降低,引入的侧丁基链作为内部增塑剂作为内部增塑剂。 与类似的分子量范围内的间隙相比,共聚物也显示出粘度降低。 这些性质使所述共聚物具有有趣的候选者在铸造应用中用作能量粘合剂。

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