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Bridging-Controlled Network Microstructure and Long-Wavelength Fluctuations in Silica-Poly(2-vinylpyridine) Nanocomposites: Experimental Results and Theoretical Analysis

机译:二氧化硅 - 聚(2-乙烯基吡啶)纳米复合材料的桥接控制网络微观结构和长波长波动:实验结果与理论分析

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摘要

We have performed small-angle X-ray scattering (SAXS) measurements to study the evolution of length-scale-dependent nanoparticle (NP) correlations over a wide range of loadings in miscible silica-poly(2-vinylpyridine) polymer nanocomposites (PNC) characterized by strong interfacial attraction. The local cage and intermediate-scale correlations evolve in a commonly observed manner with increasing silica concentration, while long-wavelength concentration fluctuations exhibit a complex behavior. Higher-loading PNCs show a nonmonotonic change in the structure factor amplitude with wavevector because of an upturn on the longest length scales, which is the most intense for the highest NP concentration sample. These observations suggest that the PNC is approaching a spinodal demixing transition of an unusual polymer bridging-induced network type. PRISM integral equation theory is quantitatively applied, captures the key features of the SAXS data, and provides a theoretical basis for a network-like phase separation analogous to polyelectrolyte coacervation. The theory with validated parameters is then used to make predictions of real-space pair correlation functions between all species, the small- and large-wavevector collective polymer structure factor, spatially resolved NP coordination numbers, the interfacial cohesive energy density, and a measure of an enlarged effective NP radius because of polymer adsorption. With increasing NP loading, intensification of tight secondary bridged NP configurations, but weakening of interpolymer and polymer-NP correlations due to packing frustration, is predicted. This local reorganization of the polymer structure coexists with macro- and microphase separation such as features at low wavevectors which vary distinctively with NP loading. The predictions for the collective polymer structure are potentially testable using scattering experiments. Our results provide an important starting point for building an understanding of collective NP dynamics.
机译:我们已经进行了小角度X射线散射(SAXS)测量,以研究在混溶性二氧化硅 - 聚(2-乙烯基吡啶)聚合物纳米复合材料(PNC)中的各种载荷上的长度依赖性纳米颗粒(NP)相关性的演变以强烈的界面吸引力为特征。局部笼和中间规模相关性以常见的方式在增加的二氧化硅浓度增加,而长波长浓度波动表现出复杂的行为。高负载PNC在最长长度尺度上显示出具有波浪传感器的结构因子幅度的非单调变化,这是最高NP浓度样品的最强烈。这些观察结果表明,PNC正在接近异常聚合物桥接诱导的网络类型的旋转晶岩脱敏转变。棱镜积分方程理论是定量应用的,捕获萨克斯数据的关键特征,并为类似于聚电解质凝聚的网络状相分离提供了理论依据。然后使用具有验证参数的理论来使所有物种,小型和大波动集体聚合物结构因子,空间分辨的NP配位数,界面内聚能密度和衡量标准的实际空间对相关函数的预测由于聚合物吸附而有效的有效NP半径。随着NP负载的增加,预测了紧缩次级桥接NP配置,但由于包装挫折而削弱互聚物和聚合物-NP相关性。该局部重组聚合物结构与宏观和微相分离共存,例如在低波浪管下的特征,其具有NP负载的优异。使用散射实验可能可测试集体聚合物结构的预测。我们的结果提供了建立对集体NP动态的理解的重要起点。

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