Brownian dynamics simulation on the parallel superposition rheology of a colloidal gel

Young Jin Lee, Howon Jin, Kyung Hyun Ahn
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Abstract

Parallel superposition rheology has been explored using Brownian dynamics simulations on a model colloidal gel by imposing a small amplitude probing oscillation parallel to the main shear flow. This study aims to investigate the constituting principles behind the material functions in parallel superposition rheometry (PSR) and to elucidate the principles behind the structure responses. The viscoelastic spectra under frequency sweeps show that in a high-frequency region, each curve can be superimposed onto a single master curve using horizontal shift factors equal to viscosity which is a reminiscence of time-shear rate superposition in orthogonal superposition rheometry. This corresponds to the region where a parallel superposition analysis can be adequately performed as the shear rate controls the viscoelastic spectra of the gel independently from probing perturbation. On the other hand, in the low-frequency region, this principle breaks down and even negative storage modulus is observed due to the strong flow coupling effect, which is also found in experiments. By introducing the spatial moduli, it is found that the negative modulus originates from the attractive potential region. In the flow conditions where negative modulus occurs, the shear force is strong enough to break down every surface bond between the particles. In this state, the increase in structural factor in response to the rise in the shear rate dominates particle stress, even within the attractive potential region. This arises because the isolated particles have more opportunities to interact with other particles as the shear rate of the imposed perturbation increases. This structural response, influenced by the attractive potential, results in a negative storage modulus and a positive loss modulus after performing Fourier transformation. This paper, for the first time by a simulation approach, demonstrates the essential characteristics of the material functions obtained using PSR. Also, this study is expected to enhance our understanding on the flowing materials and suggest a criterion for the reliable application of superposition rheology using a viscoelastic master curve.
胶体凝胶平行叠加流变的布朗动力学模拟
通过对模型胶体凝胶施加与主剪切流平行的小振幅探测振荡,利用布朗动力学模拟探索了平行叠加流变学。本研究旨在探究平行叠加流变学(PSR)中材料函数背后的构成原理,并阐明结构响应背后的原理。频率扫描下的粘弹性频谱显示,在高频区域,每条曲线都可以通过与粘度相等的水平移动因子叠加到一条主曲线上,这是对正交叠加流变仪中时间-剪切速率叠加的再现。由于剪切速率控制着凝胶的粘弹性光谱,而不受探测扰动的影响,因此在这一区域可以充分进行平行叠加分析。另一方面,在低频区域,这一原则会被打破,由于强烈的流动耦合效应,甚至会观察到负的存储模量,这在实验中也有发现。通过引入空间模量,可以发现负模量源于吸引力势区。在出现负模量的流动条件下,剪切力足以破坏颗粒之间的每一个表面键。在这种状态下,随着剪切速率的上升,结构因子的增加会主导颗粒应力,即使在吸引力势能区域内也是如此。这是因为随着外加扰动的剪切速率增加,孤立的粒子有更多机会与其他粒子相互作用。这种受吸引力影响的结构响应在进行傅立叶变换后会产生负的存储模量和正的损耗模量。本文首次通过模拟方法展示了利用 PSR 获得的材料函数的基本特征。此外,这项研究有望加深我们对流动材料的理解,并为使用粘弹性主曲线可靠地应用叠加流变学提出一个标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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