材料科学
复合材料
极限抗拉强度
韧性
涂层
复合数
弹性体
相容性(地球化学)
共晶体系
热导率
延伸率
聚合物
电阻率和电导率
聚乙烯
聚丙烯
离子电导率
电导率
艾氏冲击强度试验
聚乙二醇
爆炸物
丙烯酸
蠕动
结构材料
纳米复合材料
电解质
拉伸试验
聚烯烃
断裂韧性
作者
Hongxia Zhang,Shimin Zhang,Yibo Zhang,Fan Liao,Yanpeng Lv,Xin Ruan,Wenwen Deng,Guoqiang He,Fei Xiao,Chongwei An
标识
DOI:10.1021/acsapm.6c00083
摘要
Developing binders that integrate excellent mechanical properties with electrical conductivity is critical to meeting the urgent demand for improved safety and reduced vulnerability in HMX-based energetic composites. Herein, a synergistically enhanced elastomer, termed AAP, was fabricated via ultraviolet-initiated free radical polymerization. The synthesis involved a polymerizable deep eutectic solvent designed from acrylic acid and acryloyloxyethyltrimethylammonium chloride, further reinforced by phytic acid, which provides high hydrogen-bond density, and the cross-linker polyethylene glycol diacrylate. The resulting elastomer features a dynamic hydrogen-bond network and efficient ion-conductive pathways. Notably, the optimized sample, AAP-2, exhibits outstanding comprehensive properties, including a tensile strength of 9.38 MPa, an elongation at break of 796.55%, a toughness of 48.41 MJ·m –3, intrinsic self-healing capability, high adhesion strength with aluminum, and an electrical conductivity of 8.179 × 10 –5 S/m. When employed as a binder, AAP demonstrated excellent compatibility with HMX. The H 50 -AAP 50 composite maintained high toughness while achieving superior tensile strength compared to traditional HTPB-based composites. More importantly, owing to its intrinsic ionic conductivity, the AAP-2 coating significantly mitigated the mechanical and electrostatic sensitivities of HMX. Consequently, the electrostatic spark sensitivity threshold of the H 90 AAP 10 sample increased markedly from 0.54 J for raw HMX to 3.6 J. This work offers new insights into the design of multifunctional binders for the construction of high-performance, safe, and low-vulnerability energetic composites.
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