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聚烯烃共混物中结构弛豫的单链极限

The single chain limit of structural relaxation in a polyolefin blend.

作者信息

May Andrew F, Maranas Janna K

机构信息

Department of Chemical Engineering, The Pennsylvania State University, University Park, PA 16802, USA.

出版信息

J Chem Phys. 2006 Jul 14;125(2):24906. doi: 10.1063/1.2204034.

Abstract

The influence of composition on component dynamics and relevant static properties in a miscible polymer blend is investigated using molecular dynamics simulation. Emphasis is placed on dynamics in the single chain dilution limit, as this limit isolates the role of inherent component mobility in the polymer's dynamic behavior when placed in a blend. For our systems, a biased local concentration affecting dynamics must arise primarily from chain connectivity, which is quantified by the self-concentration, because concentration fluctuations are minimized due to restraints on chain lengths arising from simulation considerations. The polyolefins simulated [poly(ethylene-propylene) (PEP) and poly(ethylene-butene) (PEB)] have similar structures and glass transition temperatures, and all interactions are dispersive in nature. We find that the dependence of dynamics upon composition differs between the two materials. Specifically, PEB (slower component) is more influenced by the environment than PEP. This is linked to a smaller self-concentration for PEB than PEP. We examine the accuracy of the Lodge-McLeish model (which is based on chain connectivity acting over the Kuhn segment length) in predicting simulation results for effective concentration. The model predicts the simulation results with high accuracy when the model's single parameter, the self-concentration, is calculated from simulation data. However, when utilizing the theoretical prediction of the self-concentration the model is not quantitatively accurate. The ability of the model to link the simulated self-concentration with biased local compositions at the Kuhn segment length provides strong support for the claim that chain connectivity is the leading cause of distinct mobility in polymer blends. Additionally, the direct link between the willingness of a polymer to be influenced by the environment and the value of the self-concentration emphasizes the importance of the chain connectivity. Furthermore, these findings are evidence that the Kuhn segment length is the relevant length scale controlling segmental dynamics.

摘要

利用分子动力学模拟研究了组成对互溶聚合物共混物中组分动力学及相关静态性质的影响。重点关注单链稀释极限下的动力学,因为该极限隔离了聚合物在共混物中时固有组分迁移率在其动态行为中的作用。对于我们的体系,影响动力学的局部浓度偏差主要源于链连接性,其由自浓度量化,因为由于模拟考虑对链长的限制,浓度波动被最小化。所模拟的聚烯烃[聚(乙烯 - 丙烯)(PEP)和聚(乙烯 - 丁烯)(PEB)]具有相似的结构和玻璃化转变温度,且所有相互作用本质上都是色散性的。我们发现两种材料的动力学对组成的依赖性不同。具体而言,PEB(较慢的组分)比PEP受环境的影响更大。这与PEB的自浓度比PEP小有关。我们研究了Lodge - McLeish模型(基于作用于库恩链段长度的链连接性)在预测有效浓度模拟结果方面的准确性。当根据模拟数据计算该模型的单个参数自浓度时,该模型能高精度地预测模拟结果。然而,当使用自浓度的理论预测时,该模型在定量上并不准确。该模型将模拟的自浓度与库恩链段长度处的局部浓度偏差联系起来的能力,为链连接性是聚合物共混物中不同迁移率的主要原因这一说法提供了有力支持。此外,聚合物受环境影响的倾向与自浓度值之间的直接联系强调了链连接性的重要性。此外,这些发现证明库恩链段长度是控制链段动力学的相关长度尺度。

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