CHINESE JOURNAL OF ENERGETIC MATERIALS
+高级检索
新型中性大分子键合剂的合成及性能
作者:
作者单位:

湖南大学

作者简介:

通讯作者:

基金项目:


Synthesis and Properties of Novel Neutral Macromolecular Bonding Agents
Author:
Affiliation:

Hunan University

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 支撑附件
    摘要:

    为实现中性大分子键合剂结构的精确调控并提升其性能,设计合成新型单体丙烯酸氰乙酯(CEA),通过与丙烯酸羟乙酯(HEA)自由基共聚制备新型中性大分子键合剂。采用傅里叶红外、核磁对单体及聚合产物进行结构表征,测定其羟值及玻璃化转变温度(Tg)。将键合剂应用于NEPE高能推进剂配方,考察其对工艺及力学性能的影响。结果表明:CEA与HEA聚合活性匹配,无需控制投料即可获得结构均一的共聚物。该键合剂降低推进剂药浆屈服值及表观粘度,提升药浆工艺性能,且常温下推进剂药柱的拉伸强度与最大伸长率分别达0.98 MPa和70.1%,较传统键中性键合剂体系提升22.5%与27.3%。

    Abstract:

    To achieve precise structural control of neutral macromolecular bonding agents and enhance their performance, a novel monomer cyanoethyl acrylate (CEA) was designed and synthesized. Through free radical copolymerization with hydroxyethyl acrylate (HEA), a new type of neutral macromolecular bonding agent was prepared. The structures of monomers and polymer products were characterized by Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR), with hydroxyl value and glass transition temperature (Tg) determined. The bonding agent was applied to NEPE high-energy propellant formulations to investigate its effects on processing and mechanical properties. Results demonstrated that CEA and HEA exhibited matched polymerization reactivity, enabling the production of structurally homogeneous copolymers without requiring controlled feeding. This bonding agent reduced the yield value and apparent viscosity of propellant slurry, improving processing performance. Moreover, the propellant grains achieved tensile strength of 0.98 MPa and maximum elongation of 70.1% at ambient temperature, representing 22.5% and 27.3% improvements respectively compared to conventional neutral bonding agent systems.

    参考文献
    相似文献
    引证文献
文章指标
  • PDF下载次数:
  • HTML阅读次数:
  • 摘要点击次数:
  • 引用次数:
引用本文

蓝相涛,张平安,袁剑民,等. 新型中性大分子键合剂的合成及性能[J]. 含能材料,DOI:10.11943/CJEM2025132.

复制
历史
  • 收稿日期: 2025-06-19
  • 最后修改日期: 2025-08-15
  • 录用日期: 2025-08-23
  • 在线发布日期:
  • 出版日期: