变硬
材料科学
聚脲
消散
弹性体
复合材料
张力(地质)
弹性能
拉伤
能量(信号处理)
变形(气象学)
动力学(音乐)
光谱学
可塑性
傅里叶变换红外光谱
应变能
结构工程
机械
形状变化
聚合物
热塑性弹性体
纳米复合材料
材料性能
动态力学分析
作者
Gladys S.-X. Tan,Bryan H.-Y. Lim,Jet Lem,Siyu Chen,Steven E. Kooi,Carlos M. Portela,Roland G.-S. Goh,Daria V. Andreeva
标识
DOI:10.1021/acsapm.5c03694
摘要
Segmented elastomers, such as polyurea, dissipate energy through various mechanisms. Although dynamic stiffening of soft domains is often cited, growing evidence highlights the dominant role of hydrogen-bond breaking and reformation. To clarify the specific role of hard domains, we synthesized polyurea, polyurethane, and polyurethane-urea with systematically varied hard-domain order, while maintaining comparable soft-domain dynamics at a target strain rate. Microballistic impact experiments revealed two distinct dissipation regimes, with ordered polyurea performing best. FTIR spectroscopy and strain-rate-dependent cyclic tension experiments confirmed an order–disorder transition coinciding with maximum energy dissipation. These findings emphasize the role of ordered hard domains in elastomer design.
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