首页> 美国卫生研究院文献>Polymers >Synthesis and Application of Arylaminophosphazene as a Flame Retardant and Catalyst for the Polymerization of Benzoxazines
【2h】

Synthesis and Application of Arylaminophosphazene as a Flame Retardant and Catalyst for the Polymerization of Benzoxazines

机译:芳基磷脂作为苯并恶嗪聚合的阻燃剂和催化剂的合成与应用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

A novel type of phosphazene containing an additive that acts both as a catalyst and as a flame retardant for benzoxazine binders is presented in this study. The synthesis of a derivative of hexachlorocyclotriphosphazene (HCP) and meta-toluidine was carried out in the medium of the latter, which made it possible to achieve the complete substitution of chlorine atoms in the initial HCP. Thermal and flammability characteristics of modified compositions were investigated. The modifier catalyzes the process of curing and shifts the beginning of reaction from 222.0 °C for pure benzoxazine to 205.9 °C for composition with 10 phr of modifier. The additive decreases the glass transition temperature of compositions. Achievement of the highest category of flame resistance (V-0 in accordance with UL-94) is ensured both by increasing the content of phenyl residues in the composition and by the synergistic effect of phosphorus and nitrogen. A brief study of the curing kinetics disclosed the complex nature of the reaction. An accurate two-step model is obtained using the extended Prout–Tompkins equation for both steps.
机译:本研究提出了一种用作催化剂和作为苯并恶嗪粘合剂的阻燃剂的添加剂的新型磷腈。在后者的培养基中进行六氯环三膦腈(HCP)和Meta-甲苯胺的衍生物的合成,这使得可以在初始HCP中实现完全取代氯原子。研究了改性组合物的热量和可燃性特性。改性剂催化固化过程,并将反应的开始从222.0℃的反应开始,用于用10phr改性剂的组合物,将纯苯恶嗪从222.0℃下移至205.9℃。添加剂降低组合物的玻璃化转变温度。通过增加组合物中苯基残基的含量和磷和氮的协同作用,确保了既通过增加苯基残基的含量和含量的最高抗阻燃性耐火性(V-0)的成就。对固化动力学的简要研究公开了反应的复杂性质。使用两个步骤的扩展PROUT-TOMPKINS方程获得精确的两步模型。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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