具有耗竭吸引力的致密胶体悬浮液的捏合动力学和延展流变学

Diego D. Soetrisno, Carina D. V. Martínez Narváez, Mariah J. Gallegos, Vivek Sharma, J. Conrad
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摘要

我们采用滴入基底(DoS)方案,研究了在恒定体积分数 ϕ=0.40 条件下,致密胶体悬浮液的毛细管驱动的捏合动力学特性,以及聚合物诱导的耗竭相互作用。带有二甲基丙烯酰胺共聚物刷的甲基丙烯酸酯共聚物颗粒悬浮在折射率和密度匹配的 80 (w/w)% 甘油水混合物中,并加入氯化钠以筛选静电排斥。通过添加重量和分散性相同的聚丙烯酰胺聚合物,引入胶体之间的损耗吸引力。聚合物的加入会延迟并改变致密悬浮液的捏合动力学,这取决于聚合物的大小和分散度。悬浮液的延伸弛豫时间 λE 与相应聚合物溶液的归一化自由体积聚合物浓度 c/c∗ 成函数关系,表明聚合物溶液的弹性特性控制着延伸时间尺度。根据我们之前的研究结果[Soetrisno 等人,Macromolecules 56, 4919-4928 (2023)],对于稀释体系中的胶体-聚合物混合物,聚合物尺寸决定了 λE 的缩放指数,而高分散性会使 λE 的缩放从幂律过渡到线性。胶体-聚合物混合物和聚合物溶液的丝状体寿命 tf 与不含聚合物的相应流体的丝状体寿命 tf,0 进行归一化后,塌缩成一条主曲线,作为 c/c∗ 的函数。这些结果让我们深入了解了聚合物尺寸在决定胶体-聚合物混合物的捏合动力学和延伸流变学方面的作用,并进一步表明这些混合物的剪切和延伸响应可以通过两种成分的浓度分别进行调节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pinching dynamics and extensional rheology of dense colloidal suspensions with depletion attractions
We study the extensional flow properties by characterizing the capillarity-driven pinching dynamics of dense colloidal suspensions at a constant volume fraction ϕ=0.40 with polymer-induced depletion interactions using a dripping-onto-substrate (DoS) protocol. Methacrylate copolymer particles with dimethylacrylamide copolymer brushes are suspended in a refractive-index- and density-matched mixture of 80 (w/w)% glycerol in water with NaCl added to screen the electrostatic repulsions. Depletion attractions between the colloids are introduced by adding polyacrylamide polymers of weight and dispersity. The addition of polymer delays and modifies the pinch-off dynamics of the dense suspensions, depending on the size and dispersity of the polymer. The extensional relaxation time λE of suspensions collapses as a function of the normalized free volume polymer concentration c/c∗ with the corresponding polymer solutions, indicating that the elastic properties of the polymer solutions control the extensional time scale. Following the results of our previous study [Soetrisno et al., Macromolecules 56, 4919–4928 (2023)], the polymer size determines the scaling exponent of λE for colloid-polymer mixtures in the dilute regime and high dispersity shifts the concentration where the scaling of λE transitions from power-law to linear. The filament lifespans tf of colloid-polymer mixtures and of polymer solutions collapse onto a master curve as a function of c/c∗ when normalized by the filament lifespan of the corresponding fluid without polymer tf,0. These results provide insight into the role of the polymer size in dictating the pinching dynamics and extensional rheology of colloid-polymer mixtures and further suggest that the shear and extensional responses of these mixtures can be separately tuned through the concentrations of the two constituents.
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