The dynamic behavior of polyelectrolyte chains in the oligomer range is investigated with coarse-grained molecular dynamics simulation and compared to data obtained by two different experimental methods, namely capillary electrophoresis and electrophoresis NMR. We find excellent agreement of experiments and simulations when hydrodynamic interactions are accounted for in the simulations. We show that the electrophoretic mobility exhibits a maximum in the oligomer range and for the first time illustrate that this maximum is due to the hydrodynamical shielding between the chain monomers. Our findings demonstrate convincingly that it is possible to model dynamic behavior of polyelectrolytes using coarse grained models for both, the polyelectrolyte chains and the solvent induced hydrodynamic interactions.
Collapse/expansion dynamics and actuation of pH-responsive nanogels
Research Center for Advanced Science and Technology, University of Tokyo（东京大学先进科学技术研究中心）；Department of Materials Science & Engineering, Johns Hopkins University（约翰斯·霍普金斯大学材料科学与工程系）
How hydrodynamic interactions alter polymer stretching in turbulence
IITB-Monash Research Academy, Indian Institute of Technology Bombay（印度孟买理工学院-蒙纳士大学联合研究院）；Indian Institute of Technology Bombay（印度孟买理工学院）；Monash University（蒙纳士大学）；Université Côte d’Azur（蔚蓝海岸大学）
