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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Modeling the Electrostatics of Hollow Shell Suspensions: Ion Distribution, Pair Interactions, and Many-Body Effects
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Modeling the Electrostatics of Hollow Shell Suspensions: Ion Distribution, Pair Interactions, and Many-Body Effects

机译:空心壳悬浮液的静电学建模:离子分布,对相互作用和多体效应

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Electrostatic interactions play a key role in hollow shell suspensions as they determine their structure, stability, thermodynamics, and rheology and also the loading capacity of small charged species for nanoreservoir applications. In this work, fast, reliable modeling strategies aimed at predicting the electrostatics of hollow shells for one, two, and many colloids are proposed and validated. The electrostatic potential inside and outside a hollow shell with a finite thickness and a specific permittivity is determined analytically in the Debye-Huckel (DH) limit. An expression for the interaction potential between two such hollow shells is then derived and validated numerically. It follows a classical Yukawa form with an effective charge depending on the shell geometry, permittivity, and inner and outer surface charge densities. The predictions of the Ornstein-Zernike (OZ) equation with this pair potential to determine equations of state are then evaluated by comparison to results obtained with a Brownian dynamics algorithm coupled to the resolution of the linearized Poisson Boltzmann and Laplace equations (PB-BD simulations). The OZ equation based on the DLVO-like potential performs very well in the dilute regime as expected, but also quite well, and more surprisingly, in the concentrated regime in which full spheres exhibit significant many-body effects. These effects are shown to vanish for shells with small thickness and high permittivity. For highly charged hollow shells, we propose and validate a charge renormalization procedure. Finally, using PB-BD simulations, we show that the cell model predicts the ion distribution inside and outside hollow shells accurately in both electrostatically dilute and concentrated suspensions. We then determine the shell loading capacity as a function of salt concentration, volume fraction, and surface charge density for nanoreservoir applications such as drug delivery, sensing, or smart coatings.
机译:静电相互作用在中空壳悬浮液中起着关键作用,因为它们决定了其结构,稳定性,热力学和流变学,以及小型带电物质在纳米储层应用中的负载能力。在这项工作中,提出并验证了一种快速,可靠的建模策略,旨在预测一种,两种和许多胶体的空心壳的静电。在Debye-Huckel(DH)极限范围内通过解析确定了具有有限厚度和特定介电常数的空心壳体内部和外部的静电势。然后,推导并验证了两个这样的空心壳之间的相互作用势的表达式。它遵循经典的Yukawa形式,根据壳的几何形状,介电常数以及内部和外部表面电荷密度,带有有效电荷。然后,通过与布朗动力学算法与线性化泊松玻尔兹曼方程和拉普拉斯方程(PB-BD模拟)的分辨率耦合的结果进行比较,评估具有该对电位以确定状态方程的Ornstein-Zernike(OZ)方程的预测)。如预期的那样,基于DLVO的电位的OZ方程在稀溶液中的表现很好,但在全球都表现出显着的多体效应的集中状态下,也表现得非常好,而且更令人惊讶。对于具有较小厚度和高介电常数的壳,这些作用已消失。对于高荷电的空心壳,我们提出并验证了荷重归一化程序。最后,使用PB-BD模拟,我们证明了该单元模型可准确预测在静电稀释和浓缩悬浮液中空心壳内部和外部的离子分布。然后,我们确定壳载量与盐浓度,体积分数和表面电荷密度的函数关系,适用于纳米储库应用,例如药物输送,传感或智能涂层。

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