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首页> 外文期刊>The Journal of Chemical Physics >A transport model and constitutive equation for oppositely charged polyelectrolyte mixtures with application to layer-by-layer assembly
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A transport model and constitutive equation for oppositely charged polyelectrolyte mixtures with application to layer-by-layer assembly

机译:具有相对电荷的聚电解质混合物的运输模型和组成方程用施加到逐层组装

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We develop a general framework for transport of polyions, solvent and salt, with intended application to Layer-by-Layer (LbL) assembly of polyelectrolyte monolayers (PEMs). The formulation for the first time includes electrostatics, chemical potential gradients, and mechanical stress gradients as driving forces for mass transport. The general model allows all species to be mobile throughout the process and avoids the assumptions of stepwise instantaneous equilibrium and/or immobilized structures typical of previous approaches, while reducing to these models in appropriate limits. A simple constitutive equation is derived for a mixture of oppositely charged polyelectrolytes that accounts for network strand dilution and cross-chain ion pairing by appending reactive terms to the Smoluchowski probability diffusion equation for network strand end-to-end vectors. The resulting general framework encompasses the Poisson equation describing the electrostatic potential distribution, an osmotic pressure balance, a stress constitutive equation, and a generalized flux law of polymer transport. The computational domain is split into a PEM phase and an external solution phase with an appropriate boundary condition derived for the interface between the two. The mobile species (water and small salt ions) are taken to be in a state of dynamic equilibrium with their distributions enslaved to the perturbations in the two polyion compositions. The proposed model captures the swelling response of PEM films to external solutions. For the first time, we studied the effects of the temporal evolution of electrostatic and stress distribution on the rate of chain loss and absorption during rinsing and dipping of an idealized and arbitrarily selected and rigid brush layer into external solutions. The temporal evolution provides a kinetic basis for the ability of LbL films to grow under conditions that thermodynamics alone suggests would cause them to be washed away and to account for partial de
机译:我们开发了一种用于运输聚乙烯,溶剂和盐的一般框架,其预期应用于聚电解质单层(PEMS)的逐层(LBL)组件。首次制剂包括静电,化学潜在梯度和机械应力梯度作为大规模运输的驱动力。一般模型允许所有物种在整个过程中是移动的,避免逐步瞬时平衡和/或固定结构的假设,典型的先前方法,同时以适当的限制降低这些模型。通过对网络股线终端向端子向端到端向量的Smoluchowski概率扩散方程附加反应性术语来衍生出对网络链稀释和交联离子配对的相反电荷的聚电解质的混合物来衍生出简单的组成方程。所得到的一般框架包括描述静电电位分布,渗透压平衡,应力本构体等式和聚合物转运的广义助焊剂定律的泊松方程。计算域被分成PEM阶段和外部解决方案阶段,其具有用于两者之间接口的适当边界条件。将移动物种(水和小盐离子)采用动态平衡状态,其分布酶酶活化为两种聚硫代组合物中的扰动。所提出的模型捕获PEM电影对外部解决方案的溶胀响应。我们首次研究了静电和应力分布的时间演化对漂洗和浸渍过程中的链损和吸收速率的影响,并将理想化的和任意选择和刚性刷层中的外部溶液中的浸渍和浸渍。时间进化为LBL薄膜在单独的热力学建议的条件下生长的能力提供了动力学基础,这将导致它们被冲走并考虑部分de

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