11,113 research outputs found

    Lasing from single, stationary, dye-doped glycerol/water microdroplets located on a superhydrophobic surface

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    We report laser emission from single, stationary, Rhodamine B-doped glycerol/water microdroplets located on a superhydrophobic surface. In the experiments, a pulsed, frequency-doubled Nd:YAG laser operating at 532 nm was used as the excitation source. The microdroplets ranged in diameter from a few to 20 um. Lasing was achieved in the red-shifted portion of the dye emission spectrum with threshold fluences as low as 750 J/cm2. Photobleaching was observed when the microdroplets were pumped above threshold. In certain cases, multimode lasing was also observed and attributed to the simultaneous lasing of two modes belonging to different sets of whispering gallery modes.Comment: to appear in Optics Communication

    Evaporation-triggered microdroplet nucleation and the four life phases of an evaporating Ouzo drop

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    Evaporating liquid droplets are omnipresent in nature and technology, such as in inkjet printing, coating, deposition of materials, medical diagnostics, agriculture, food industry, cosmetics, or spills of liquids. While the evaporation of pure liquids, liquids with dispersed particles, or even liquid mixtures has intensively been studied over the last two decades, the evaporation of ternary mixtures of liquids with different volatilities and mutual solubilities has not yet been explored. Here we show that the evaporation of such ternary mixtures can trigger a phase transition and the nucleation of microdroplets of one of the components of the mixture. As model system we pick a sessile Ouzo droplet (as known from daily life - a transparent mixture of water, ethanol, and anise oil) and reveal and theoretically explain its four life phases: In phase I, the spherical cap-shaped droplet remains transparent, while the more volatile ethanol is evaporating, preferentially at the rim of the drop due to the singularity there. This leads to a local ethanol concentration reduction and correspondingly to oil droplet nucleation there. This is the beginning of phase II, in which oil microdroplets quickly nucleate in the whole drop, leading to its milky color which typifies the so-called 'Ouzo-effect'. Once all ethanol has evaporated, the drop, which now has a characteristic non-spherical-cap shape, has become clear again, with a water drop sitting on an oil-ring (phase III), finalizing the phase inversion. Finally, in phase IV, also all water has evaporated, leaving behind a tiny spherical cap-shaped oil drop.Comment: 40 pages, 12 figure

    Can hail and rain nucleate cloud droplets?

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    We present results from moist convection in a mixture of pressurized sulfur hexa-flouride (liquid and vapor) and helium (gas) to model the wet and dry components of the earth's atmosphere. To allow for homogeneous nucleation, we operate the experiment close to critical conditions. We report on the nucleation of microdroplets in the wake of large cold liquid drops falling through the supersaturated atmosphere and show that the homogeneous nucleation is caused by isobaric cooling of the saturated sulfur hexaflouride vapor. Our results carry over to atmospheric clouds: falling hail and cold rain drops may enhance the heterogeneous nucleation of microdroplets in their wake under supersaturated atmospheric conditions. We also observed that under appropriate conditions settling microdroplets form a rather stable horizontal cloud layer, which separates regions of super and sub critical saturation.Comment: 6 pages, 3 figure

    Mist Flow Visualization for Round Jets in Aerosol Jet Printing

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    With the microdroplets of water serving as light scattering particles, the mist flow patterns of round micro-jets can be visualized using the Aerosol Jet(R) direct-write system. The visualization images show that the laminar mist jet appears to extend to more than 20 times the diameter of nozzle orifice, D, for jet Reynolds number Re < 600, especially with D = 0.3 mm and less. For smaller jets (e.g., with D = 0.15 mm), laminar collimated mist flow might be retained to 40xD for Re < 600 and for Re ~ 1500 within 20xD from the nozzle. The laminar part of mist flow associated with larger jets (e.g., with D = 1.0 mm for Re < 600) tends to exhibit noticeable gradual widening due to viscous diffusion. For free jets, their breakdown length--the distance from nozzle where transition from laminar to turbulent mist flow takes place as signaled by the inception of a rapid widening of mist stream--is shown to decrease with increasing Re. The presence of impingement wall tends to prevent turbulence development, even when the wall is placed further downstream of the free-jet breakdown length for a given Re . The critical Re for an impinging jet to develop turbulence increases as the standoff S is reduced. The mist flow of impinging jet of D = 1.0 mm seems to remain laminar even for Re > 4000 at S = 12 mm.Comment: 12 pages, 10 figure

    Frequency effect on streaming phenomenon induced by Rayleigh surface acoustic wave in microdroplets

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    Acoustic streaming of ink particles inside a water microdroplet generated by a surface acoustic wave(SAW) has been studied numerically using a finite volume numerical method and these results have been verified using experimental measurements. Effects of SAW excitation frequency, droplet volume, and radio-frequency (RF) power are investigated, and it has been shown that SAW excitation frequency influences the SAWattenuation length, lSAW , and hence the acoustic energy absorbed by liquid. It has also been observed that an increase of excitation frequency generally enhances the SAW streaming behavior. However, when the frequency exceeds a critical value that depends on the RF power applied to the SAW device, weaker acoustic streaming is observed resulting in less effective acoustic mixing inside the droplet. This critical value is characterised by a dimensionless ratio of droplet radius to SAWattenuation length, i.e., Rd/lSAW . With a mean value of Rd/lSAW  ≈ 1, a fast and efficient mixing can be induced, even at the lowest RF power of 0.05 mW studied in this paper. On the other hand, for the Rd/lSAW ratios much larger than ∼1, significant decreases in streaming velocities were observed, resulting in a transition from regular (strong) to irregular (weak) mixing/flow. This is attributed to an increased absorption rate of acoustic wave energy that leaks into the liquid, resulting in a reduction of the acoustic energy radiated away from the SAW interaction region towards the droplet free surface. It has been demonstrated in this study that a fast and efficient mixing process with a smaller RF power could be achieved if the ratio of Rd/lSAW  ≤ 1 in the SAW-droplet based microfluidics

    Microfluidic generation of networked droplet collections and lipid membrane constructs

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    We report on microfluidic strategies to generate several multi-compartment membrane-based structures, including droplet interface bilayer networks and multi-compartment vesicles. These developments allow the current status quo— where microdroplets are used as isolated vessels— to be changed. By linking droplets together with lipid membranes, higher order systems can be generated, with particular ramifications for bottom-up synthetic biology and for functional droplet-based microreactors and biodevices

    A method for volume stabilization of single, dye-doped water microdroplets with femtoliter resolution

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    A self-control mechanism that stabilizes the size of Rhodamine B-doped water microdroplets standing on a superhydrophobic surface is demonstrated. The mechanism relies on the interplay between the condensation rate that was kept constant and evaporation rate induced by laser excitation which critically depends on the size of the microdroplets. The radii of individual water microdroplets (>5 um) stayed within a few nanometers during long time periods (up to 455 seconds). By blocking the laser excitation for 500 msec, the stable volume of individual microdroplets was shown to change stepwise.Comment: to appear in the J. Op. Soc. Am.
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