The temperature-dependent ballistic performance and the ductile-to-brittle transition in polymer networks

被引:17
|
作者
Masser, Kevin A. [1 ]
Long, Tyler R. [1 ]
Yu, Jian H. [1 ]
Knorr, Daniel B., Jr. [1 ]
Hindenlang, Mark D. [1 ]
Taylor, Terrence [1 ]
Harris, Doug [1 ]
Lenhart, Joseph L. [1 ]
机构
[1] US Army, Res Lab, CCDEVCOM, Weap & Mat Res Directorate, Aberdeen, MD 21010 USA
关键词
ballistic; ductile-to-brittle transition; impact; polymer network; DYNAMIC GLASS-TRANSITION; MOLECULAR-DYNAMICS; CHARACTERISTIC LENGTH; MECHANICAL-BEHAVIOR; MOBILITY; DEFORMATION; RELAXATION; TOUGHNESS; SCALE; ARCHITECTURE;
D O I
10.1002/polb.24807
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The temperature dependence of the ballistic impact performance of a series of transparent polymer networks is evaluated. A systematic series of homogeneous epoxy/propylene-oxide-based thermosets, a nanoscale phase-separated epoxy/dual amine thermoset, and two homogeneous, completely aliphatic materials synthesized via ring-opening metathesis polymerization are examined. The Vogel temperature (T-o) and the Kauzmann temperature (T-K) are critical parameters for scaling the temperature-dependent ballistic impact performance of each class of materials. The ductile-to-brittle transition temperature in a series of propylene-oxide amine-cured epoxies occurs at the material T-K, corresponding to a sharp drop in fracture toughness and ballistic impact performance. Two aliphatic, ring-opening metathesis polymerized materials are found to exhibit no clear transition from purely ductile to purely brittle behavior, but the temperature dependence is still scaled to a single curve when normalized by T-o. The cooperatively rearranging region (CRR) or the volume of this region is related to the breadth of temperatures over which these materials exhibit purely ductile deformation both quasi-statically and at higher rates. The temperature-dependent performance is discussed in the context of the configurational entropy. The breadth of the ductility window is related to the size of the CRR, calculated from calorimetric measurements at the resin T-g. Published 2019. This article is a U.S. Government work and is in the public domainin the USA. J. Polym. Sci., Part B: Polym. Phys. 2019, 57, 511-523
引用
收藏
页码:511 / 523
页数:13
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