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一种用于添加盐的悬浮液中高电荷胶体(微凝胶)的自洽奥恩斯坦-泽尔尼克凝胶模型。

A self-consistent Ornstein-Zernike jellium for highly charged colloids (microgels) in suspensions with added salt.

作者信息

Aguirre-Manzo L A, González-Mozuelos P

机构信息

Departamento de Física, Cinvestav del I. P. N., Av. Instituto Politécnico Nacional 2508, Ciudad de México, C. P. 07360, Mexico.

出版信息

J Phys Condens Matter. 2021 May 28;33(27). doi: 10.1088/1361-648X/abfe95.

Abstract

This work discusses a jellium scheme, built within the framework of the multicomponent Ornstein-Zernike (OZ) equation, which is capable of describing the collective structure of suspensions of highly charged colloids with added salt, even in the presence of finite-size multivalent microions. This approach uses a suitable approximation to decouple the microion-microion correlations from the macroion-microion profiles, which in combination with the methodology from the dressed ion theory (DIT) gives a full account of the electrostatic effective potential among the colloids. The main advantages of the present contribution reside in its ability to manage the short-range potentials and non-linear correlations among the microions, as well as its realistic characterization of the ionic clouds surrounding each macroion. The structure factors predicted by this jellium scheme are contrasted with previously reported experimental results for microgel suspensions with monovalent salts (2019032602), thus validating its high accuracy in these situations. The present theoretical analysis is then extended to microgel suspensions with multivalent salts, which reveals the prominent influence of the counterion valence on the makeup of the effective potentials. Although the induced differences may be difficult to identify through the mesoscopic structure, our results suggest that the microgel collapsing transition may be used to enhance these distinct effects, thus giving a feasible experimental probe for these phenomena.

摘要

这项工作讨论了一种在多组分奥恩斯坦 - 泽尔尼克(OZ)方程框架内构建的凝胶模型,该模型能够描述添加盐的高电荷胶体悬浮液的集体结构,即使存在有限尺寸的多价微离子。这种方法使用了一种合适的近似来将微离子 - 微离子相关性与大离子 - 微离子分布解耦,这与修饰离子理论(DIT)的方法相结合,全面考虑了胶体之间的静电有效势。本研究的主要优点在于其处理微离子间短程势和非线性相关性的能力,以及对每个大离子周围离子云的实际表征。该凝胶模型预测的结构因子与先前报道的单价盐微凝胶悬浮液的实验结果(2019032602)进行了对比,从而验证了其在这些情况下的高精度。然后,本理论分析扩展到多价盐微凝胶悬浮液,揭示了抗衡离子价对有效势组成的显著影响。尽管通过介观结构可能难以识别诱导差异,但我们的结果表明,微凝胶塌陷转变可用于增强这些明显的效应,从而为这些现象提供一种可行的实验探针。

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