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Two-particle interfacial microrheology at polymer-polymer interfaces

机译:聚合物-聚合物界面的两粒子界面微流变学

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摘要

We continue to develop two-particle interfacial microrheology and have applied the technique to study the interfacial viscoelastic properties of immiscible poly(dimethylsiloxane) (PDMS)-poly(ethylene glycol) (PEG) interfaces. The interfacial storage and loss moduli are measured over a wide frequency range: at low frequencies, the interfaces are dominated by viscous responses whereas elasticity dominates at high frequencies. The zero-shear interfacial viscosity, estimated following the Cox-Merz rule and Cross model, falls between the bulk viscosities of the two individual polymers. Surprisingly, the interfacial relaxation time, calculated from the crossover of the storage and loss moduli, is observed to be an order of magnitude larger than that of the PDMS bulk polymers. The effects of tracer particle surface chemistry and size have also been investigated and show minimum influences on two-particle interfacial microrheology.
机译:我们继续开发两粒子界面微流变学,并将该技术应用于研究不相溶的聚二甲基硅氧烷(PDMS)-聚乙二醇(PEG)界面的界面粘弹性。界面存储和损耗模量在很宽的频率范围内测量:在低频下,界面受粘滞响应支配,而弹性在高频下支配。遵循Cox-Merz规则和Cross模型估算的零剪切界面粘度介于两种单独聚合物的体积粘度之间。出乎意料的是,观察到由储能和损耗模量的交点计算的界面弛豫时间比PDMS本体聚合物的界面弛豫时间大一个数量级。还研究了示踪剂颗粒表面化学性质和尺寸的影响,并显示出对两颗粒界面微流变学的最小影响。

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