Tension Amplification in Tethered Layers of Bottle-Brush Polymers

被引:18
|
作者
Leuty, Gary M. [1 ,4 ]
Tsige, Mesfin [1 ]
Grest, Gary S. [2 ]
Rubinstein, Michael [3 ]
机构
[1] Univ Akron, Dept Polymer Sci, Akron, OH 44325 USA
[2] Sandia Natl Labs, Albuquerque, NM 87185 USA
[3] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[4] US Air Force, Res Lab, Mat & Mfg Directorate, Wright Patterson AFB, OH 45433 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
COMPUTER-SIMULATIONS; MOLECULAR BRUSHES; DYNAMICS; ADSORPTION; COPOLYMERS; MELTS; GLYCOSAMINOGLYCANS; POLYELECTROLYTES; MACROMOLECULES; LUBRICATION;
D O I
10.1021/acs.macromol.5b02305
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Molecular dynamics simulations of a coarse-grained bead spring model have been used to study the effects of molecular crowding on the accumulation of tension in the backbone of bottle-brush polymers tethered to a flat substrate. The number of bottle -brushes per unit surface area, Sigma, as well as the lengths of the bottle-brush backbones N-bb (so <= N-bb <= 200) and side chains N-sc (50 <= N-sc <= 200) were varied to determine how the dimensions and degree of crowding of bottle -brushes give rise to bond tension amplification along the backbone, especially near the substrate. From these simulations, we have identified three separate regimes of tension. For low Sigma, the tension is due solely to intramolecular interactions and is dominated by the side chain repulsion that governs the lateral brush dimensions. With increasing Sigma, the interactions between bottle-brush polymers induce compression of the side chains, transmitting increasing tension to the backbone. For large Sigma, intermolecular side chain repulsion increases, forcing side chain extension and reorientation in the direction normal to the surface and transmitting considerable tension to the backbone.
引用
收藏
页码:1950 / 1960
页数:11
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