...
首页> 外文期刊>Propellants, Explosives, Pyrotechnics >Propiolate-Terminated Polybutadiene-Based Network Binders for Solid Propellants via Catalyst-Free Azide-Alkyne Cycloaddition
【24h】

Propiolate-Terminated Polybutadiene-Based Network Binders for Solid Propellants via Catalyst-Free Azide-Alkyne Cycloaddition

机译:丙炔酸封端聚丁二烯基网络粘合剂,通过无催化剂叠氮化物-炔烃环加成制备固体推进剂

获取原文
获取原文并翻译 | 示例

摘要

We developed the new preparation method of polybutadiene-based binders, which has been widely used in solid composite propellants, under the triazole curing system formed by the Huisgen azide-alkyne cycloaddition (AAC) without any promotors. Firstly, polybutadiene terminated with propiolate, alkyne adjacent to electron-withdrawing group-C(=O)O-, PKPB(propiolate-terminated polybutadiene), was prepared followed by the 1,3-cycloaddition with trivalent azide curatives leading to form the polybutadiene binder cured via triazole linkages. Unexpectedly, compared to the conventional urethane-cured binders, higher temperature and long time were required to cure the polybutadiene binder and the mechanical properties, especially tensile strength was not as good as that of binder formed under urethane curing system. For the tria- zole-cured polybutadiene binder to exhibit the better mechanical properties, an asymmetric difunctional chain-linker end-capped with an alkyne and an isocyanate, respectively was introduced to modify the end-groups of hydroxyl-ter-minated polybutadiene (HTPB) with propiolates, ester al-kynes, resulting in forming the propiolate-terminated poly-urethane butadiene (PTPUB). The triazole-cured polyurethane butadiene-based binders obtained from the click reaction of PTPUB with tri-azide curatives conveyed the excellent mechanical properties as well as considerable shortening of reaction time, compared to PKPB-based binders. Finally, both of triazole cured binders showed the good low-temperature properties, Tg, available for solid propellants.
机译:在Huisgen azide-alkyne cyclazenation(AAC)形成的三唑固化体系下,我们开发了聚丁二烯基粘结剂的新制备方法,该粘结剂已广泛应用于固体复合推进剂中,没有任何促进剂。首先,制备了与丙炔酸酯封端的聚丁二烯,丙炔烯相邻的吸电子基团-C(=O)O-,PKPB(丙炔酸封端聚丁二烯),然后用三价叠氮化物固化剂制备1,3-环加成,形成通过三唑键固化的聚丁二烯粘结剂。出乎意料的是,与传统的聚氨酯固化粘结剂相比,聚丁二烯粘结剂的固化温度更高,时间更长,机械性能,特别是拉伸强度不如聚氨酯固化体系下形成的粘结剂。为了使三唑固化的聚丁二烯粘结剂表现出更好的力学性能,引入一种不对称的双官能团链连接剂,分别用炔烃和异氰酸酯封端,用丙炔酸酯改性羟基叔丁二烯(HTPB)的端基,形成丙炔酸酯封端的聚氨基甲酸酯丁二烯(PTPUB)。与PKPB基粘结剂相比,PTPUB与三叠氮化固化剂的点击反应得到的三唑固化聚氨酯丁二烯基粘结剂具有优异的力学性能和显著缩短的反应时间。最后,两种三唑固化粘结剂都表现出良好的低温性能Tg,可用于固体推进剂。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号