Tumbling and Deformation of Isolated Polymer Chains in Shearing Flow

被引:48
作者
Dalal, Indranil Saha [1 ]
Albaugh, Alex [1 ]
Hoda, Nazish [1 ]
Larson, Ronald G. [1 ]
机构
[1] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
BROWNIAN DYNAMICS SIMULATIONS; SEMIFLEXIBLE POLYMERS; DNA; DILUTE;
D O I
10.1021/ma3014349
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Using Brownian dynamics simulations of polymer chains over a wide range of resolution, we find universal scaling laws for polymer coil dimensions and tumbling time. At high shear rates (gamma) over dot, the coil thickness in the gradient direction becomes independent of chain length, scaling as N-kappa(0)(gamma) over dot(-1/4), where N-kappa denotes the numbers of Kuhn steps, and the tumbling time scales as N-kappa(gamma) over dot(-3/4), correcting scaling laws presented in prior studies. We find this to be a consequence of the formation of loops whose length is limited by the time required to stretch them and derive scaling laws from a balance of convection and diffusion of monomers. We find that, in the absence of hydrodynamic interaction (HI) and excluded volume (EV), for wormlike chains, the shrinkage in chain stretch observed at ultrahigh shear rates is pushed out to arbitrarily high shear rates if the chain is resolved increasingly finely below the persistence length. Finally, scaling laws in the presence of excluded volume and hydrodynamic interactions are derived that are expected to be valid for long chains at high shear rates.
引用
收藏
页码:9493 / 9499
页数:7
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