Multiscale Formulation for Assessment of Electroosmotic Flow in Paper-Based Microfluidics.

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Joselynne C Salazar Bove, Sebastian Toro, Pablo A Kler
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引用次数: 0

Abstract

In this work, multiscale techniques to model the pressure driven and electroosmotic flows in porous materials with paper-like microstructures are studied and applied. The multiscale technique is based on the definition of a representative volume element (RVE) of the material, where the microstructure is built from connected channels, where the fluid moves inside the void of the porous material. For fluid flow, the velocity is solved under incompressible flow conditions in the Stokes regime at the microscale level, while the homogeneous Darcy problem is solved at the macroscale level. Similarly, for electroosmotic flow, the velocity and pressure are also solved at the microscale under incompressible flow conditions in the Stokes regime. However, in this case a Helmholtz-Smoluchowsky term is considered at the surface of the solid microstructure. Such term is calculated by solving the electric field via the charge conservation equation. Consequently, the electroosmotic velocity is included in the fluid dynamic problem as a boundary condition, significantly reducing the computational demand. Afterward, once the homogenized velocity field of the microscale problem is obtained, an effective pressure-based permeability and an effective electroosmotic permeability are estimated at the macroscale. To validate the results, a comparison is made with experimental data and other numerical studies reported in the literature for common papers used in microfluidics, such as Whatman # $\#$ 1 and Munktel 00A, but also through comparisons with direct numerical simulations. Finally, we propose a microcell structure for representing such papers for matching fluid flow and electrical properties. With such topology, electroosmotic and mixed fluid flow are solved in order to demonstrate the capabilities of the multiscale technique for representing different phenomena involved in paper-based microfluidics. With these microcells will be also possible to predict other physicochemical phenomena which are important for paper-based microfluidics such as capillary imbibition or scalar dispersion, among others.

基于纸张的微流体中电渗透流动评估的多尺度公式。
在本工作中,研究并应用了多尺度技术来模拟具有纸状微结构的多孔材料中的压力驱动和电渗透流动。多尺度技术是基于材料的代表性体积元(RVE)的定义,其中微观结构是由连接的通道构建的,流体在多孔材料的空隙中移动。对于流体流动,在微观尺度上求解不可压缩流动条件下的Stokes格式下的速度,在宏观尺度上求解齐次Darcy问题。同样,对于电渗透流动,在不可压缩流动条件下的速度和压力也可以在微观尺度上求解。然而,在这种情况下,在固体微观结构的表面考虑Helmholtz-Smoluchowsky项。这一项是通过电荷守恒方程求解电场来计算的。因此,将电渗透速度作为边界条件纳入流体动力学问题,大大减少了计算量。然后,一旦获得微观尺度问题的均匀速度场,就可以在宏观尺度上估计有效的基于压力的渗透率和有效的电渗透渗透率。为了验证结果,将实验数据与微流体常用论文(如whatman# $\#$ 1和Munktel 00A)中报道的其他数值研究进行了比较,并与直接数值模拟进行了比较。最后,我们提出了一个微细胞结构来表示这些论文,以匹配流体流动和电学性质。利用这种拓扑结构,解决了电渗透和混合流体流动问题,以展示多尺度技术表征纸基微流体中不同现象的能力。有了这些微细胞,还可以预测其他对纸基微流体很重要的物理化学现象,如毛细管吸胀或标量分散等。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
期刊介绍: ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.
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