电不稳定性混沌的Lorenz模型。

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Prateek Gupta, Supreet Singh Bahga
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引用次数: 0

摘要

我们证明了洛伦兹方程组可以近似于微通道中电不稳定性(EKI)的非线性流动动力学,该微通道由电场驱动,电场平行于分离具有不匹配电导率的共流动中心流和鞘流的扩散界面。利用伽辽金投影,我们证明了电流体动力流动方程可以用洛伦兹方程近似地表示在流体间电导率差很小的极限下。导出的动力学模型定性地捕捉了EKI在线性和非线性状态下的特征,包括中性稳定性判据和随着电瑞利数的增加在周期和非周期状态之间的交替转换。虽然在数量上不精确,但这个简化的动力学模型为在EKI实验中观察到的混沌行为的基本非线性提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lorenz Model for Chaos in Electrokinetic Instability.

We demonstrate that the Lorenz system of equations can approximate the nonlinear flow dynamics of the electrokinetic instability (EKI) in a microchannel driven by an electric field applied parallel to the diffusive interfaces separating the co-flowing centre and sheath streams with mismatched electrical conductivity. Using Galerkin projection, we show that the electrohydrodynamic flow equations can be approximated by the Lorenz equations in the limit of small conductivity difference between the flow streams. The derived dynamical model qualitatively captures the characteristics of EKI in both linear and nonlinear regimes, including the neutral stability criterion and alternating transitions between periodic and aperiodic states with increasing electric Rayleigh numbers. While not quantitatively precise, this simplified dynamical model provides valuable insights into the essential nonlinearities responsible for chaotic behaviour observed in EKI experiments.

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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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