Mechanical Properties of Glassy Polyethylene Nanofibers via Molecular Dynamics Simulations

被引:33
作者
Buell, Sezen [2 ]
Van Vliet, Krystyn J. [2 ]
Rutledge, Gregory C. [1 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
关键词
TRANSITION TEMPERATURE; ELASTIC PROPERTIES; POLYMER; MODULI; DEFORMATION; SCAFFOLDS;
D O I
10.1021/ma900250y
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 extent to which the intrinsic mechanical properties of polymer fibers depend on physical size has been a matter of dispute that is relevant to most nanofiber applications. Here, we report the elastic and plastic properties determined from molecular dynamics simulations of amorphous, glassy polymer nanofibers with diameter ranging from 3.7 to 17.7 nm. We find that, for a given temperature, the Young's elastic modulus E decreases with Fiber radius and can be as much as 52% lower than that of the corresponding bulk material. Poisson's ratio nu of the polymer comprising these nanofibers was found to decrease from a value of 0.3 to 0.1 with decreasing fiber radius. Our findings also indicate that a small but finite stress exists on the simulated nanofibers prior to elongation, attributable to surface tension. When strained uniaxially tip to a tensile strain of epsilon = 0.2 over the range of strain rates and temperatures considered, the nanofibers exhibit a yield stress ay between 40 and 72 MPa, which is not strongly dependent oil fiber radius; this yield stress is approximately half that of the same polyethylene simulated in the amorphous bulk.
引用
收藏
页码:4887 / 4895
页数:9
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