Predicting reaction behavior of tethered polymers in shear flow

被引:0
|
作者
Nguyen, Anh Hung [1 ]
Kania, Sagar [1 ]
Oztekin, Alparslan [1 ]
Webb III, Edmund B. [1 ]
机构
[1] Lehigh Univ, Dept Mech Engn & Mech, Bethlehem, PA 18015 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2023年 / 159卷 / 17期
基金
美国国家科学基金会;
关键词
VON-WILLEBRAND-FACTOR; COLLAPSED POLYMERS; HYDRODYNAMIC INTERACTIONS; FACTOR MULTIMERS; DYNAMICS; CLEAVAGE; SURFACE; LENGTH; DNA; SIMULATION;
D O I
10.1063/5.0168440
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
Kinetics of force-mediated chemical reactions of end-tethered polymers with varying chain length N in varying shear rate flow gamma are explored via coarse-grained Brownian dynamics simulations. At fixed gamma , force F along a polymer increases linearly with N as previously predicted; however, contrary to existing theory, the F(N) slope increases for N above a transition length that exhibits minimal dependence on gamma . Force profiles are used in a stochastic model of a force-mediated reaction to compute the time for x percent of a polymer population to experience a reaction, t(x). Observations are insensitive to the selected value of x in that t(x) data for varying N and gamma can be consistently collapsed onto a single curve via appropriate scaling, with one master curve for systems below the transition N (small N) and another for those above (large N). Different force scaling for small and large N results in orders of magnitude difference in force-mediated reaction kinetics as represented by the population response time. Data presented illustrate the possibility of designing mechano-reactive polymer populations with highly controlled response to flow across a range in gamma
引用
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页数:9
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