Lin Y-H, Huang C-F
Department of Applied Chemistry, National Chiao Tung University, Hsinchu, Taiwan.
J Chem Phys. 2008 Jun 14;128(22):224903. doi: 10.1063/1.2927870.
The dynamic structure factor (DSF) for single (labeled) chains well entangled in polymer melts has been developed based on the Rouse-Mooney picture; the DSF functions derived from the Langevin equations of the model in both discrete and continuous forms are given. It is shown that for all practical purposes, it is sufficient to use the continuous form to analyze experimental results in the "safe" q region (q being the magnitude of the scattering wave vector q) where the Rouse-segment-based theories are applicable. The DSF form reduces to the same limiting form as that of the free Rouse chain as q(2)a(2) or q(2)R(2)-->infinity (a and R being the entanglement distance and the root mean square end-to-end distance, respectively), confirming what has been expected physically. The natural reduction to the limiting form allows the full range of DSF curves to be displayed in terms of the reduced Rouse variable q(2)(Z(d)t)(0.5) in a unified way. The displayed full range represents a framework or "map," with respect to which effects occurring in different regions of the DSF may be located and studied in a consistent manner. One effect is the significant or noticeable deviations of the theoretical DSF curves from the limiting curve in the region approximately 4>q(2)(Z(d)t)(0.5)> approximately 0.1 (a time region where t<tau(1) (e)) to the faster side as qa is in the range 1-5. This is supported by the comparison of the experimental results of an entangled poly(vinylethylene) sample with the theoretical curves. The DSF functional forms predict plateaus with heights depending on the value of q-q-split plateaus-as can be experimentally observed in the time region greater than the relaxation time tau(1) (e) of the lowest Rouse-Mooney mode, when qa falls between approximately 1 and approximately 7. High sensitivity of the distribution of the q-split plateaus to a enables its value to be extracted from matching the calculated with the experimental results. The thus obtained a value for a well-entangled poly(ethylene-co-butene) polymer is in close agreement with the rheological result. It is shown that the fixed-end boundary conditions in the Rouse-Mooney model are responsible for the correct prediction of the distribution of the q-split plateaus.
基于劳斯-穆尼图景,已针对聚合物熔体中高度缠结的单(标记)链开发了动态结构因子(DSF);给出了从该模型的朗之万方程以离散和连续形式导出的DSF函数。结果表明,对于所有实际应用而言,在基于劳斯链段的理论适用的“安全”q区域(q为散射波矢q的大小)中,使用连续形式来分析实验结果就足够了。当q²a²或q²R²趋于无穷大时(a和R分别为缠结距离和均方根端到端距离),DSF形式简化为与自由劳斯链相同的极限形式,这证实了物理上的预期。自然地简化为极限形式使得能够以统一的方式根据约化的劳斯变量q²(Zd t)⁰·⁵来展示DSF曲线的全范围。所展示的全范围代表了一个框架或“图谱”,据此可以以一致的方式定位和研究在DSF的不同区域中出现的效应。一种效应是在大约4 > q²(Zd t)⁰·⁵ > 大约0.1的区域(即t < τ₁(e)的时间区域)中,理论DSF曲线相对于极限曲线有显著或明显的偏差,偏向较快的一侧,此时qa在1 - 5范围内。缠结的聚(乙烯-乙烯基醚)样品的实验结果与理论曲线的比较支持了这一点。DSF函数形式预测了具有取决于q - q分裂平台值的高度的平台——这在大于最低劳斯-穆尼模式的弛豫时间τ₁(e)的时间区域中可以通过实验观察到,当qa介于大约1和大约7之间时。q分裂平台的分布对a的高灵敏度使得能够通过将计算结果与实验结果匹配来提取其值。由此获得的高度缠结的聚(乙烯-共-丁烯)聚合物的a值与流变学结果非常吻合。结果表明,劳斯-穆尼模型中的固定端边界条件负责正确预测q分裂平台的分布。