Scale-dependent particle diffusivity and apparent viscosity in polymer solutions as probed by dynamic magnetic nanorheology

热扩散率 粘度 粒子(生态学) 聚合物 比例(比率) 材料科学 热力学 化学物理 化学 物理 复合材料 地质学 海洋学 量子力学
作者
Melissa Hess,Micha Gratz,Hilke Remmer,Samira Webers,Joachim Landers,Dmitry Borin,Frank Ludwig,Heiko Wende,Stefan Odenbach,Andreas Tschöpe,Annette M. Schmidt
出处
期刊:Soft Matter [Royal Society of Chemistry]
卷期号:16 (32): 7562-7575 被引量:23
标识
DOI:10.1039/c9sm00747d
摘要

In several upcoming rheological approaches, including methods of micro- and nanorheology, the measurement geometry is of critical impact on the interpretation of the results. The relative size of the probe objects employed (as compared to the intrinsic length scales of the sample to be investigated) becomes of crucial importance, and there is increasing interest to investigate the dynamic processes and mobility in nanostructured materials. A combination of different rheological approaches based on the rotation of magnetically blocked nanoprobes is used to systematically investigate the size-dependent diffusion behavior in aqueous poly(ethylene glycol) (PEG) solutions with special attention paid to the relation of probe size to characteristic length scales within the polymer solutions. We employ two types of probe particles: nickel rods of hydrodynamic length Lh between 200 nm and 650 nm, and cobalt ferrite spheres with diameter dh between 13 nm and 23 nm, and examine the influence of particle size and shape on the nanorheological information obtained in model polymer solutions based on two related, dynamic-magnetic approaches. The results confirm that as long as the investigated solutions are not entangled, and the particles are much larger than the macromolecular correlation length, a good accordance between macroscopic and nanoscopic results, whereas a strong size-dependent response is observed in cases where the particles are of similar size or smaller than the radius of gyration Rg or the correlation length ξ of the polymer solution.

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