聚脲
材料科学
复合材料
聚氨酯
应变率
分离式霍普金森压力棒
弹性体
软化
压缩永久变形
热塑性聚氨酯
压力(语言学)
热固性聚合物
变形(气象学)
无定形固体
粘弹性
天然橡胶
哲学
有机化学
化学
语言学
作者
Yi Jing,Mary C. Boyce,G.F. Lee,Edward Balizer
出处
期刊:Polymer
[Elsevier]
日期:2006-01-01
卷期号:47 (1): 319-329
被引量:393
标识
DOI:10.1016/j.polymer.2005.10.107
摘要
The thermoplastic elastomer polyurethane and the elastomeric thermoset polyurea are finding new applications in increasing the survivability of structures under impact loading, including those encountered in blast and ballistic events. However, the mechanical behavior of polyurea and polyurethane materials under these high rate conditions is relatively unknown. Here, the rate-dependent stress–strain behavior of one polyurea and three representative polyurethane materials is studied by dynamic mechanical analysis, quasi-static compression testing and split Hopkinson pressure bar (SHPB) testing. The polyurethane chemistries were chosen to probe the influence of the hard segment content on the mechanical behavior, where the volume fraction and the amorphous vs. crystalline structure of the hard segment domains were varied. The large strain stress–strain behavior of polyurea and polyurethane shows strong hysteresis, cyclic softening, and strong rate-dependence. The polyurethane with a non-crystalline well-dispersed hard segment morphology did not exhibit cyclic softening. The materials are observed to transition from a rubbery-like behavior under low strain rate (∼10−3–100 s−1) loading conditions to either a leathery or glassy-like behavior under high strain rate (∼10−3 s−1) loading conditions.
科研通智能强力驱动
Strongly Powered by AbleSci AI