Quantifying deformation and energy dissipation of polymeric surfaces under localized impact

被引:41
|
作者
Constantinides, Georgios [1 ]
Tweedie, Catherine A. [1 ]
Holbrook, Doria M. [2 ]
Barragan, Patrick [2 ]
Smith, James F. [3 ]
Van Vlietl, Krystyn J. [1 ]
机构
[1] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
[2] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
[3] Micro Mat Ltd, Wrexham, Wales
关键词
polymers; impact; nanoindentation;
D O I
10.1016/j.msea.2007.12.044
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The mechanical response of polymeric surfaces to concentrated impact loads is relevant to a range of applications, but cannot be inferred from quasistatic or oscillatory contact loading. Here we propose and demonstrate a set of quantitative metrics that characterizes the ability of polymers to resist impact deformation and dissipate impact energy, as well as the strain rate sensitivity of these materials to contact loading. A model which incorporates nonlinear material behavior is presented and can predict the experimentally observed deformation behavior with high accuracy. The micrometer-scale impact response of several polymers has been investigated in the velocity range of 0.7-1.5 mm/s. Two semi-crystalline polymers - polyethylene (PE) and polypropylene (PP) - characterized above the corresponding glass transition temperature T-g, and four fully amorphous polymers characterized well below T-g-polystyrene (PS), polycarbonate (PC), and low and high molecular weight poly(methyl methacrylate) or PMMA termed commercially as Lucite (R) (LU) and Plexiglas (R) (PL) - have been considered. In an inverse application, the model and experimental method provide a tool for extracting the relevant material quantities, including energy dissipation metrics such as the coefficient of restitution e. This approach can be used to determine quantitatively the impact energy absorption of polymer surfaces at elevated temperatures through T-g, as demonstrated for PS and PC over the range of 20-180 degrees C. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:403 / 412
页数:10
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