High-Order Multiple Emulsions Formed in Poly(dimethylsiloxane) Microfluidics

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Birgit Hausmann
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A. R. Abate and D. A. Weitz "High-Order Multiple Emulsions Formed in Poly(dimethylsiloxane) Microfluidics" Small 5(18), 2030-2032 (2009)


microfluidics, multiple emulsions, photoresponsive materials, sol–gel processes, wettability


Droplets encapsulated multiple times in droplets of alternating kinds of fluids (oil, water) were emulsified in a highly controlled way. PDMS microcapillary devices were used to guarantee monodispersity of higher order emulsions, at the expense of large quantity formation.

Results and Discussion

Fig. 1 Ordered droplets (water and oil, alternating) formed by linear drop maker arrays. Photomicrographs of a) single, b) double, c) triple, d)quadruple, and e)quintuple emulsion drop maker arrays.The multiple emulsions produced by the arrays are shown to the right. (The scalebars are 100mm.)
Fig. 2 Hexagonally packed a) single, c) double, e) triple, g) quadruple, and i) quintuple emulsions in a monolayer. The diameter distributions are shown for the b) single, d) double, f) triple, h) quadruple, and j) quintuple emulsions; the distributions for the outer drops and each of the nested inner drops are plotted individually.

A single emulsion of water droplets in fluorocarbon oil (w/o) is formed by injecting water at 200mL/h in the first inlet of a microtube and oil in a second inlet at 400mL/h (Fig. 1a). The single drop maker has uniform hydrophobic wettability. To form a double emulsion of o/w/o a third inlet is added to the linear drop maker where the fluid is injected at 600mL/h (Fig. 1b). By adding even more inlets and triggering the fluid speeds at each inlet even triple, quadruple and quintuple emulsion were formed (Fig. 1c-e).

In that way monodisperse higher order emulsion can be formed. Since the microcapillary devices fabrication is very difficult the scalability of the emulsification process is restricted. Linear arrays of poly(dimethylsiloxane) (PDMS) drop makers with alternating wettability were fabricated such that drops form from each channel.

A superior method would combine the control of microfluidic drop formation with increased scalability. method here combines the control of microfluidic drop formation with the scalability of lithographically fabricated devices.[10] We use

For the drop formation junction, we use pinned-jet flow focusing (PJFF). To form a double emulsion, we require two drop makers functionalized to have opposite wettability. the first hydrophilic and the second hydrophobic. to perfectly synchronize the devices, we hydrodynamically couple them using triggered drop formation. We design each nozzle such that it is slightly narrower than the incoming emulsion from the previous drop maker. This allows the incoming emulsion to obstruct the nozzle, perturbing flow, and triggering the formation of the outer drop Weconfine our drops in a monolayer by sandwiching them between two plates that are 50mmapart. diameter distribution is narrow, with coefficient of variation (CV) of 2%, Similarly, the triple, quadruple, and quintuple emulsions all pack hexagonally because all are monodisperse

The emulsions pack hexagonally because they areconfinedinamonolayerandmonodisperse.

Experimental Section Preparation of devices: The devices are fabricated using softlithography in PDMS. [10] All devices are fabricated at a fixed channel height of 50 mm. The PDMS devices are bonded to a glass plate using oxygen-plasma treatment To spatially control wettability, the devices are coated with a photoreactive sol–gel [11] within 15 minutes after plasma bonding. The devices are filled with the photoreactive sol–gel mixture and heated with a hotplate set to 225 8C; this vaporizes the solvent in the mixture and deposits the coating. The coating makes the channels hydrophobic by default; to spatially pattern wettability, we graft patches of hydrophilic polyacrylic acid onto the interface using utraviolet (UV) light-initiated polymerization. To accomplish this we fill the coated channels with the hydrophilic monomer solution and expose them to spatially patterned UV light. When exposed to light, the photoinitiator silanes embedded in the sol–gel release radicals that initiate polymerization of the acrylic acid monomers in solution. The resulting acrylic acid polymers are grafted to the sol–gel interface, tethered by covalent linkages with the photoinitiator silanes. This results in a dense covering of polyacrylic acid of the interface, making it very hydrophilic, suitable for forming oil-in-water emulsions.