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1.
J Colloid Interface Sci ; 486: 265-276, 2017 Jan 15.
Article in English | MEDLINE | ID: mdl-27721075

ABSTRACT

Three dimensional simulations are performed to investigate the interaction dynamics between two drops impinging simultaneously on a dry surface. Of particular interest in this study is to understand the effects of impact velocity and surrounding gas density on droplet interactions. To simulate the droplet dynamics and morphologies, a computational framework based on the phase-field lattice Boltzmann formulation is employed for the two-phase flow computations involving high density ratio. Two different coalescence modes are identified when the impinging droplets have different impact speeds. When one of the droplet has a tangential impact velocity component, asymmetric ridge formation is observed. Influence of droplet impact angle on the interaction dynamics of the central ridge is further investigated. Traces of different fluid particles are seeded to analyse internal flow dynamics in oblique impact scenarios. Greater overlapping between the fluid particles is observed with increase in the impact angle. Finally, the present simulations indicate that the ambient gas density has a significant influence to determine the final outcome of the droplet interactions.

2.
Phys Rev E ; 94(2-1): 023108, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27627393

ABSTRACT

The behavior of a droplet impinging onto a solid substrate can be influenced significantly by the horizontal motion of the substrate. The coupled interactions between the moving wall and the impacting droplet may result in various outcomes, which may be different from the usual normal droplet impact on a stationary wall. In this paper, we present a method to suppress drop rebound on hydrophobic surfaces via transverse wall oscillations, normal to the impact direction. The numerical investigation shows that the suppression of droplet rebound has a direct relationship with the oscillation phase, amplitude, and frequency. For a particular range of oscillation frequencies and amplitudes, a lateral shifting of the droplet position is observed along the oscillating direction. While large oscillation amplitude favors the process of droplet deposition, a high frequency promotes droplet rebound from the oscillating wall. A linear trend in the transition region between deposition and rebound is observed from a scaled phase diagram of the oscillation amplitude versus frequency. We provide a systematic investigation of drop deposition and elucidate the mechanism of rebound suppression through the temporal evolution of the nonaxial kinetic energy and the velocity flow field.

3.
J Biomech Eng ; 130(3): 031018, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18532867

ABSTRACT

Micropatterning of two different cell types based on surface modification allows spatial control over two distinct cell subpopulations. This study considers a micropatterned coculture system, which has release and absorption parts alternately arranged at the base, and each part has a single cell type. A micropattern unit was defined and within each unit, there are one release part and one absorption part. The cells in the absorption parts consume species, which are secreted by the cells in the release parts. The species concentrations at the micropatterned cell base were computed from a three-dimensional numerical flow model incorporating mass transport. Different combined parameters were developed for the release and absorption parts to make the data collapse in each part. Combination of the collapse data in the release and absorption parts can be used to predict the concentration distribution through the whole channel. The correlated results were applied to predict the critical length ratio of the release and absorption parts for an actual micropatterned system (Bhatia et al., 1999, "Effect of Cell-Cell Interactions in Preservation of Cellular Phenotype: Co-Cultivation of Hepatocytes and Nonparenchymal Cell," FASEB J. 13, pp. 1883-1900) to avoid species insufficiency based on basic fibroblast growth factor (bFGF). The mass transfer effectiveness was found to be higher with more numbers of micropattern units. The optimal condition for micropatterned coculture bioreactors is achieved by having the product of the length ratio and the reaction ratio equal to 1. This condition was used to optimize the mass transfer in the micropatterned system (Bhatia et al., 1999, "Effect of Cell-Cell Interactions in Preservation of Cellular henotype: Co-Cultivation of Hepatocytes and Nonparenchymal Cell," FASEB J. 13, pp. 1883-1900) based on bFGF.


Subject(s)
Bioreactors , Coculture Techniques/methods , Fibroblast Growth Factor 2/metabolism , Microfluidic Analytical Techniques/methods , Numerical Analysis, Computer-Assisted , Paracrine Communication , Animals , Cells, Cultured , Coculture Techniques/instrumentation , Computer Simulation , Diffusion Chambers, Culture , Equipment Design , Fibroblast Growth Factor 2/analysis , Fibroblasts/cytology , Fibroblasts/metabolism , Hepatocytes/cytology , Hepatocytes/metabolism , Humans , Kinetics , Microfluidic Analytical Techniques/instrumentation , Models, Biological
4.
J Biomech Eng ; 129(3): 365-73, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17536903

ABSTRACT

Microchannel bioreactors have applications for manipulating and investigating the fluid microenvironment on cell growth and functions in either single culture or co-culture. This study considers two different types of cells distributed randomly as a co-culture at the base of a microchannel bioreactor: absorption cells, which only consume species based on the Michaelis-Menten process, and release cells, which secrete species, assuming zeroth order reaction, to support the absorption cells. The species concentrations at the co-culture cell base are computed from a three-dimensional numerical flow-model incorporating mass transport. Combined dimensionless parameters are proposed for the co-culture system, developed from a simplified analysis under the condition of decreasing axial-concentration. The numerical results of species concentration at the co-culture cell-base are approximately correlated by the combined parameters under the condition of positive flux-parameter. Based on the correlated results, the critical value of the inlet concentration is determined, which depends on the effective microchannel length. For the flow to develop to the critical inlet concentration, an upstream length consisting only of release cells is needed; this upstream length is determined from an analytical solution. The generalized results may find applications in analyzing the mass transport requirements in a co-culture microchannel bioreactor.


Subject(s)
Biological Transport, Active , Bioreactors , Cell Culture Techniques/instrumentation , Cell Physiological Phenomena , Microfluidic Analytical Techniques/instrumentation , Animals , Cell Culture Techniques/methods , Cells, Cultured , Coculture Techniques , Computer Simulation , Humans , Kinetics , Microfluidic Analytical Techniques/methods
5.
J Biomech Eng ; 128(2): 185-93, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16524329

ABSTRACT

Microchannel bioreactors have been used in many studies to manipulate and investigate the fluid microenvironment around cells. In this study, substrate concentrations and shear stresses at the base were computed from a three-dimensional numerical flow-model incorporating mass transport. Combined dimensionless parameters were developed from a simplified analysis. The numerical results of substrate concentration were well correlated by the combined parameters. The generalized results may find applications in design analysis of microchannel bioreactors. The mass transport and shear stress were related in a generalized result. Based on the generalized results and the condition of dynamic similarity, various means to isolate their respective effects on cells were considered.


Subject(s)
Bioreactors , Cell Culture Techniques/instrumentation , Cell Physiological Phenomena , Computer-Aided Design , Flow Injection Analysis/instrumentation , Microfluidic Analytical Techniques/instrumentation , Models, Biological , Animals , Biological Transport, Active , Cell Culture Techniques/methods , Cells, Cultured , Computer Simulation , Equipment Design , Equipment Failure Analysis , Flow Injection Analysis/methods , Humans , Kinetics , Microfluidic Analytical Techniques/methods , Shear Strength , Stress, Mechanical
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