Sun Qi, Faller Roland
Department of Chemical Engineering and Materials Science, University of California at Davis, Davis, California 95616, USA.
J Chem Phys. 2007 Apr 14;126(14):144908. doi: 10.1063/1.2715588.
The authors have successfully developed a structurally coarse-grained 1,4-cis-polyisoprene-atactic polystyrene blend model by systematic mapping between a detailed atomistic model and a mesoscale model. This is to their best knowledge the first time that a chemically specific polymer blend model has been used to study the phase separation morphology and kinetics in a blend. A structurally optimized force-field model has many advantages over simple bead-spring models in terms of representing the chain microstructure. It keeps the identity of the polymers, particularly the structure through radial distribution functions. Starting from randomly mixed initial configurations, the blends show a clear phase separation for chain lengths around 10 monomers and this separation becomes more pronounced with the increase of chain length. The ensuing morphology is lamellar at equiweight concentrations and cylindrical or spherical at unbalanced concentrations. Morphologies are validated to be stable under increasing system sizes and further characterized quantitatively by density profiles.
作者通过在详细的原子模型和中尺度模型之间进行系统映射,成功开发了一种结构粗粒化的1,4-顺式聚异戊二烯-无规立构聚苯乙烯共混物模型。据他们所知,这是首次使用化学特异性聚合物共混物模型来研究共混物中的相分离形态和动力学。在表示链微观结构方面,结构优化的力场模型比简单的珠簧模型具有许多优势。它保持了聚合物的特性,特别是通过径向分布函数体现的结构。从随机混合的初始构型开始,对于链长约为10个单体的情况,共混物显示出明显的相分离,并且随着链长的增加,这种分离变得更加明显。在等重浓度下,随后的形态是层状的,在不平衡浓度下是柱状或球状的。形态在系统尺寸增加时被验证是稳定的,并通过密度分布进行了进一步的定量表征。