FLUID MIXING USING INDUCED CHARGE ELECTRO-OSMOTIC TRANSVERSE FLOW ACTUATED BY ASYMMETRICAL DRIVING ELECTRODE SEQUENCE

Microfluid mixing is an essential process in chemical analysis, drug test, and nanoparticle synthesis. Induced charge electro-osmosis (ICED) has good capability in microfluid mixing for its reconfigurable vortex profile. We found experimentally ICEO transverse flow induced by the asymmetrical driving electrode has a good performance in disturbing the interface of two fluids. Encouraged by these aspects, we proposed a micromixer using ICEO transverse flows actuated by the asymmetrical driving electrode sequence to mix microfluids. We established a simulation model to investigate the evolution ofthe interface and demonstrate the work principle of this method. Moreover, we numerically explored the effects of device structure, and electrolyte characteristics on the capability of micromixer Finally, we validated this method experimentally, and studied the effects of voltage intensity, frequency and flow rate on the mixing capability, obtaining mixing efficiency exceeding 94%. This method is a potential alternative in various microfluidic and lab-on-a-chip applications.</p

Microparticle separation using asymmetrical induced-charge electro-osmotic vortices on an arc-edge-based floating electrode

Five arc-shaped gaps were designed on the bipolar electrode to actuate alternately opposite-direction asymmetrical induced-charge electro-osmosis (AICEO) vortices, and we developed a microfluidic device using such asymmetrical vortices to realize particle separation. When the buoyancy force dominates in the vertical direction, particles stay at the channel bottom, experiencing a left deflection under the vortices in the convex arc areas. In contrast, when the levitation force induced by AICEO vortices overcomes the buoyancy force, particles are elevated to a high level and captured by right vortices, undergoing a right deflection under the vortices in the concave arc areas. Moreover, when particles pass through the concave or convex arc areas every time, their right or left deflections are enlarged gradually and the separation becomes more complete. Remarkably, as the light/small particles at low voltage, heavy/large particles can be elevated to a new high level and undergo right deflection by increasing the voltage. We first explicitly proved the separation principle and analyzed numerically its capability in density- and size-based separation. Depending on the study of the voltage-dependent AICEO characterization of 4 mu m silica and 4 mu m PMMA particles, we experimentally verified the feasibility of our device in density-based separation. According to the investigation of sensitivity to particle size, we separated multi-sized yeast cells to confirm the capability of our device in size-based separation. Finally, we extracted yeast cells from impeding particles, obtaining 96% purity. Additionally, we designed a 500 mu m distance between the focusing and separation region to circumvent the problems caused by electric-field interaction. Our AICEO-based separation method holds potential to serve as a useful tool in transesterification of microalgal lipids to biodiesel and solar cell processing because of its outstanding advantages, such as gentle conditions, contact-free separation, high-sensitivity and high-efficiency separation capability.</p

A microscopic physical description of electrothermal-induced flow for control of ion current transport in microfluidics interfacing nanofluidics

The phenomenon of electrothermal (ET) convection has recently captured great attention for transporting fluidic samples in microchannels embedding simple electrode structures. In the classical model of ET-induced flow, a conductivity gradient of buffer medium is supposed to arise from temperature-dependent electrophoretic mobility of ionic species under uniform salt concentrations, so it may not work well in the presence of evident concentration perturbation within the background electrolyte. To solve this problem, we develop herein a microscopic physical description of ET streaming by fully coupling a set of Poisson-Nernst-Planck-Navier-Stokes equations and temperature-dependent fluid physicochemical properties. A comparative study on a standard electrokinetic micropump exploiting asymmetric electrode arrays indicates that, our microscopic model always predicts a lower ET pump flow rate than the classical macroscopic model even with trivial temperature elevation in the liquid. Considering a continuity of total current density in liquids of inhomogeneous polarizability, a moderate degree of fluctuation in ion concentrations on top of the electrode array is enough to exert a significant influence on the induction of free ionic charges, rendering the enhanced numerical treatment much closer to realistic experimental measurement. Then, by placing a pair of thin-film resistive heaters on the bottom of an anodic channel interfacing a cation-exchange medium, we further provide a vivid demonstration of the enhanced model's feasibility in accurately resolving the combined Coulomb force due to the coexistence of an extended space charge layer and smeared interfacial polarizations in an externally-imposed temperature gradient, while this is impossible with conventional linear approximation. This leads to a reliable method to achieve a flexible regulation on spatial-temporal evolution of ion-depletion layer by electroconvective mixing. These results provide useful insights into ET-based flexible control of micro/nanoscale solid entities in modern micro-total-analytical systems