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稳态剪切流作用下纤维素纳米原纤静电稳定悬浮液的微观力学

Micro-mechanics of electrostatically stabilized suspensions of cellulose nanofibrils under steady state shear flow.

作者信息

Martoïa F, Dumont P J J, Orgéas L, Belgacem M N, Putaux J-L

机构信息

Univ. Grenoble Alpes, LGP2, F-38000 Grenoble, France.

出版信息

Soft Matter. 2016 Feb 14;12(6):1721-35. doi: 10.1039/c5sm02310f. Epub 2016 Jan 4.

Abstract

In this study, we characterized and modeled the rheology of TEMPO-oxidized cellulose nanofibril (NFC) aqueous suspensions with electrostatically stabilized and unflocculated nanofibrous structures. These colloidal suspensions of slender and wavy nanofibers exhibited a yield stress and a shear thinning behavior at low and high shear rates, respectively. Both the shear yield stress and the consistency of these suspensions were power-law functions of the NFC volume fraction. We developed an original multiscale model for the prediction of the rheology of these suspensions. At the nanoscale, the suspensions were described as concentrated systems where NFCs interacted with the Newtonian suspending fluid through Brownian motion and long range fluid-NFC hydrodynamic interactions, as well as with each other through short range hydrodynamic and repulsive colloidal interaction forces. These forces were estimated using both the experimental results and 3D networks of NFCs that were numerically generated to mimic the nanostructures of NFC suspensions under shear flow. They were in good agreement with theoretical and measured forces for model colloidal systems. The model showed the primary role played by short range hydrodynamic and colloidal interactions on the rheology of NFC suspensions. At low shear rates, the origin of the yield stress of NFC suspensions was attributed to the combined contribution of repulsive colloidal interactions and the topology of the entangled NFC networks in the suspensions. At high shear rates, both concurrent colloidal and short (in some cases long) range hydrodynamic interactions could be at the origin of the shear thinning behavior of NFC suspensions.

摘要

在本研究中,我们对具有静电稳定且未絮凝的纳米纤维结构的TEMPO氧化纤维素纳米纤丝(NFC)水悬浮液的流变学特性进行了表征并建立了模型。这些由细长且呈波浪状的纳米纤维组成的胶体悬浮液在低剪切速率和高剪切速率下分别表现出屈服应力和剪切变稀行为。这些悬浮液的剪切屈服应力和稠度均为NFC体积分数的幂律函数。我们开发了一种用于预测这些悬浮液流变学的原始多尺度模型。在纳米尺度上,悬浮液被描述为浓缩体系,其中NFC通过布朗运动以及流体与NFC之间的长程流体动力学相互作用与牛顿悬浮液相互作用,并且通过短程流体动力学和排斥性胶体相互作用力彼此相互作用。利用实验结果和通过数值生成以模拟剪切流下NFC悬浮液纳米结构的NFC三维网络来估算这些力。它们与模型胶体系统的理论力和测量力高度吻合。该模型显示了短程流体动力学和胶体相互作用对NFC悬浮液流变学的主要作用。在低剪切速率下,NFC悬浮液屈服应力的起源归因于排斥性胶体相互作用以及悬浮液中缠结的NFC网络拓扑结构的综合贡献。在高剪切速率下,同时存在的胶体相互作用和短程(某些情况下为长程)流体动力学相互作用可能是NFC悬浮液剪切变稀行为的起源。

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