Zhang Wenlin, Larson Ronald G
Department of Chemical Engineering, University of Michigan, Ann Arbor, Michigan 48109, United States.
ACS Cent Sci. 2018 Nov 28;4(11):1545-1550. doi: 10.1021/acscentsci.8b00651. Epub 2018 Nov 6.
We use an analytical mean-field theory and all-atom molecular dynamics (MD) simulations to predict that external tension, together with the nematic coupling interactions, can drive phase separation of long chains from short ones in bidisperse homopolymer melts. The nematic coupling parameter α for polyethylene (PE) oligomers under applied tension is extracted from the MD simulations and used in the mean-field free energy to predict the phase boundary for bidisperse melts in which the longer chains are stretched by uniaxial tension. The predicted phase diagram is validated by direct MD simulations. We also show that extensional flow, and possibly even shear flow, may lead to nematic phase separation in molten PE oligomers, because the flow can impose a stronger tension on the longer chains than the short ones.
我们使用解析平均场理论和全原子分子动力学(MD)模拟来预测,外部张力与向列耦合相互作用一起,可以驱动双分散均聚物熔体中长链与短链的相分离。通过MD模拟提取了施加张力下聚乙烯(PE)低聚物的向列耦合参数α,并将其用于平均场自由能中,以预测双分散熔体的相边界,其中较长的链被单轴张力拉伸。预测的相图通过直接MD模拟得到验证。我们还表明,拉伸流动,甚至可能是剪切流动,可能导致熔融PE低聚物中的向列相分离,因为流动对较长链施加的张力比对短链更强。