Crazing of nanocomposites with polymer-tethered nanoparticles

被引:32
|
作者
Meng, Dong [1 ,5 ]
Kumar, Sanat K. [1 ]
Ge, Ting [2 ]
Robbins, Mark O. [3 ]
Grest, Gary S. [4 ]
机构
[1] Columbia Univ, Dept Chem Engn, New York, NY 10027 USA
[2] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[3] Johns Hopkins Univ, Dept Phys & Astron, Baltimore, MD 21218 USA
[4] Sandia Natl Labs, POB 5800, Albuquerque, NM 87185 USA
[5] Mississippi State Univ, Dave C Swalm Sch Chem Engn, Starkville, MS 39762 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2016年 / 145卷 / 09期
基金
美国国家科学基金会;
关键词
MECHANICAL-PROPERTIES; PHASE-BEHAVIOR; FRACTURE; COMPOSITES; FAILURE; ENTANGLEMENTS; SIMULATIONS; SURFACE;
D O I
10.1063/1.4961872
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The crazing behavior of polymer nanocomposites formed by blending polymer grafted nanoparticles with an entangled polymer melt is studied by molecular dynamics simulations. We focus on the three key differences in the crazing behavior of a composite relative to the pure homopolymer matrix, namely, a lower yield stress, a smaller extension ratio, and a grafted chain length dependent failure stress. The yield behavior is found to be mostly controlled by the local nanoparticle-grafted polymer interfacial energy, with the grafted polymer-polymer matrix interfacial structure being of little to no relevance. Increasing the attraction between nanoparticle core and the grafted polymer inhibits void nucleation and leads to a higher yield stress. In the craze growth regime, the presence of "grafted chain" sections of approximate to 100 monomers alters the mechanical response of composite samples, giving rise to smaller extension ratios and higher drawing stresses than for the homopolymer matrix. The dominant failure mechanism of composite samples depends strongly on the length of the grafted chains, with disentanglement being the dominant mechanism for short chains, while bond breaking is the failure mode for chain lengths >10N(e), where N-e is the entanglement length. Published by AIP Publishing.
引用
收藏
页数:10
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