LeDuc P, Haber C, Bao G, Wirtz D
Department of Mechanical Engineering, The Johns Hopkins University, Baltimore, Maryland 21218, USA.
Nature. 1999 Jun 10;399(6736):564-6. doi: 10.1038/21148.
Polymer dynamics are of central importance in materials science, mechanical engineering, biology and medicine. The dynamics of macromolecular solutions and melts in shear flow are typically studied using bulk experimental methods such as light and neutron scattering and birefringence. But the effect of shear on the conformation and dynamics of individual polymers is still not well understood. Here we describe observations of the real-time dynamics of individual, flexible polymers (fluorescently labelled DNA molecules) under a shear flow. The sheared polymers exhibit many types of extended conformation with an overall orientation ranging from parallel to perpendicular with respect to the flow direction. For shear rates much smaller than the inverse of the relaxation time of the molecule, the relative populations of these two main types of conformation are controlled by the rate of the shear flow. These results question the adequacy of assumptions made in standard models of polymer dynamics.
聚合物动力学在材料科学、机械工程、生物学和医学中至关重要。大分子溶液和熔体在剪切流中的动力学通常使用诸如光散射、中子散射和双折射等整体实验方法进行研究。但是,剪切对单个聚合物的构象和动力学的影响仍未得到很好的理解。在此,我们描述了在剪切流下单个柔性聚合物(荧光标记的DNA分子)的实时动力学观察结果。被剪切的聚合物呈现出多种类型的伸展构象,其整体取向相对于流动方向从平行到垂直不等。对于远小于分子弛豫时间倒数的剪切速率,这两种主要构象类型的相对数量由剪切流速率控制。这些结果对聚合物动力学标准模型中所做假设的充分性提出了质疑。