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首页> 外文期刊>Propellants, Explosives, Pyrotechnics >Synthesis and Characterization of Glycidyl Azide-r-(3,3-bis(azidomethyl)oxetane)Copolymers
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Synthesis and Characterization of Glycidyl Azide-r-(3,3-bis(azidomethyl)oxetane)Copolymers

机译:缩水甘油叠氮基-r-(3,3-双(叠氮基甲基)氧杂环丁烷)共聚物的合成与表征

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Glycidyl azide-r-(3,3-bis(azidomethyl)oxetane)copolymers were synthesized by cationic copolymerization of epichlorohydrin and 3,3-bis(bromomethyl)oxetane,using butane-1,4-diol as an initiator and boron trifluoride etherate as a catalyst,followed by azidation of the halogenated copolymer.The main objective of this work is the preparation of an OH-terminated amorphous polymer with energetic content higher than that of the well-known glycidyl azide homopolymer.The effect of experimental conditions,i.e.,the rate of monomer feeding,on the final molecular weight and functionality of the copolymer has also been investigated.The obtained copolymers were extensively characterized to determine their composition and thermal stability.The heat of reaction for the polymerization of the halogenated key precursors has also been measured.It was found that even though both the operating conditions and the catalytic system were chosen in order to favor a living character of the polymerization,the final product seems to be the result of a combined living and active chain end mechanism.In particular,the latter is responsible for the formation of oligomers and not hydroxyl-terminated chains.Nevertheless,the average number of OH groups is high enough to allow a cross-linking of the polymeric chains,by addition of polyisocyanates and subsequent formation of inter-chain urethanic bonds.
机译:通过环氧氯丙烷与3,3-双(溴甲基)氧杂环丁烷的阳离子共聚反应,使用丁烷-1,4-二醇作为引发剂和三氟化硼醚化物,合成了叠氮化缩水甘油-r-(3,3-双(叠氮甲基)氧杂环丁烷)共聚物。作为催化剂,接着进行了卤代共聚物的叠氮化。这项工作的主要目的是制备一种高能含量比众所周知的缩水甘油基叠氮化物均聚物高的OH封端的无定形聚合物。此外,还研究了单体进料速率对共聚物最终分子量和官能度的影响。对所得共聚物进行了广泛的表征,以确定其组成和热稳定性。卤化关键前体的聚合反应热也得到了确定。结果发现,即使同时选择了操作条件和催化体系以利于聚合的活性,最终的产物似乎是活的和活泼的链端机制相结合的结果。特别是,后者负责形成低聚物而不是羟基封端的链。尽管如此,OH基的平均数目仍然足够高,可以交叉。通过添加多异氰酸酯并随后形成链间氨基甲酸酯键,使聚合物链发生-连接。

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