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      Droplet breakup driven by shear thinning solutions in a microfluidic T-Junction

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          Abstract

          Droplet microfluidics is, like a miniaturized biomedical lab, efficient and adjustable for high throughput analysis, encapsulation of cells, drug formulation, polymerase chain reaction. Typically, for most biomedical applications, handling of complex, non-Newtonian fluids is involved, e.g. synovial and salivary fluids, collagen, gel scaffolds. The role of the corresponding rheology on the droplets breakup has not been accurately addressed so far. Here we suggest a novel approach to describe droplets formation occurring in a microfluidic T-shaped junction, either in Newtonian or non-Newtonian, shear thinning liquids. The non-Newtonian liquid carrying the droplets was made of Xanthan solutions, a stiff rod-like polysaccharide displaying a marked shear thinning rheology and weak elastic effects. The breakup process shows similar trends regardless of the nature of the surrounding liquid once the droplets size is assessed in terms of an effective Capillary number introduced to account for shear thinning effects. Experimental results are complemented with numerical simulations of pure power-law fluids with the lattice Boltzmann models, which are in good quantitative agreement with the experimental data and confirm the proposed scaling.

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          Most cited references20

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          Microfluidic diagnostic technologies for global public health.

          The developing world does not have access to many of the best medical diagnostic technologies; they were designed for air-conditioned laboratories, refrigerated storage of chemicals, a constant supply of calibrators and reagents, stable electrical power, highly trained personnel and rapid transportation of samples. Microfluidic systems allow miniaturization and integration of complex functions, which could move sophisticated diagnostic tools out of the developed-world laboratory. These systems must be inexpensive, but also accurate, reliable, rugged and well suited to the medical and social contexts of the developing world.
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            Formation of droplets and bubbles in a microfluidic T-junction-scaling and mechanism of break-up.

            This article describes the process of formation of droplets and bubbles in microfluidic T-junction geometries. At low capillary numbers break-up is not dominated by shear stresses: experimental results support the assertion that the dominant contribution to the dynamics of break-up arises from the pressure drop across the emerging droplet or bubble. This pressure drop results from the high resistance to flow of the continuous (carrier) fluid in the thin films that separate the droplet from the walls of the microchannel when the droplet fills almost the entire cross-section of the channel. A simple scaling relation, based on this assertion, predicts the size of droplets and bubbles produced in the T-junctions over a range of rates of flow of the two immiscible phases, the viscosity of the continuous phase, the interfacial tension, and the geometrical dimensions of the device.
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              Lattice Boltzmann simulations of droplet formation in a T-shaped microchannel.

              We investigated the formation of a droplet from a single pore in a glass chip, which is a model system for droplet formation in membrane emulsification. Droplet formation was simulated with the lattice Boltzmann method, a method suitable for modeling on the mesoscale. We validated the lattice Boltzmann code with several benchmarks such as the flow profile in a rectangular channel, droplet deformation between two shearing plates, and a sessile drop on a plate with different wetting conditions. In all cases, the modeling results were in good agreement with the benchmark. A comparison of experimental droplet formation in a microchannel glass chip showed good quantitative agreement with the modeling results. With this code, droplet formation simulations with various interfacial tensions and various flow rates were performed. All resulting droplet sizes could be correlated quantitatively with the capillary number and the fluxes in the system.
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                Author and article information

                Journal
                2016-10-25
                Article
                1610.07800
                13d744cf-9ded-431b-8444-0b45d9a63222

                http://arxiv.org/licenses/nonexclusive-distrib/1.0/

                History
                Custom metadata
                Manuscript: 9 pages 5 figures, 61 References. Supplementary Material: 5 pages 1 figure, two movies
                cond-mat.soft

                Condensed matter
                Condensed matter

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