Materials Research and Innovation Laboratory (MRAIL), Department of Chemical and Biomolecular Engineering, University of Tennessee, Knoxville, Tennessee 37996, USA.
J Chem Phys. 2018 Apr 14;148(14):141103. doi: 10.1063/1.5026792.
Virtual experimentation of atomistic entangled polyethylene melts undergoing planar elongational flow revealed an amazingly detailed depiction of individual macromolecular dynamics and the resulting effect on bistable configurational states. A clear coil-stretch transition was evident, in much the same form as first envisioned by de Gennes for dilute solutions of high polymers, resulting in an associated hysteresis in the configurational flow profile over the range of strain rates predicted by theory. Simulations conducted at steady state revealed bimodal distribution functions, in which equilibrium configurational states were simultaneously populated by relatively coiled and stretched molecules which could transition from one conformational mode to the other over a relatively long time scale at critical values of strain rates. The implication of such behavior points to a double-well conformational free energy potential with an activation barrier between the two configurational minima.
原子纠缠聚乙烯熔体在平面拉伸流中进行的虚拟实验揭示了对单个高分子动力学的惊人详细描述,以及对双稳态构象状态的影响。可以明显看出,线圈拉伸转变与 de Gennes 最初设想的高聚物稀溶液中的形式非常相似,导致在理论预测的应变率范围内,构形流曲线的滞后现象与理论预测一致。在稳态下进行的模拟揭示了双峰分布函数,其中平衡构象状态同时由相对卷曲和拉伸的分子占据,这些分子可以在临界应变率下在相对较长的时间尺度上从一种构象模式转变为另一种构象模式。这种行为的含义表明存在双势阱构象自由能,其中两个构象极小值之间存在一个活化能垒。