Why Bubbles Coalesce Faster than Droplets: The Effects of Interface Mobility and Surface Charge.

Air bubbles in pure water appear to coalesce much faster compared to oil emulsion droplets at the same water solution conditions. The main factors explaining this difference in coalescence times could be interface mobility and/or pH-dependent surface charge at the water interface. To quantify the relative importance of these effects, we use high-speed imaging to monitor the coalescence of free-rising air bubbles with the water-air interface as well as free-falling fluorocarbon-oil emulsion droplets with a water-oil interface.

Interferometry and Simulation of the Thin Liquid Film between a Free-Rising Bubble and a Glass Substrate.

Because of their practical importance and complex underlying physics, the thin liquid films formed between colliding bubbles or droplets have long been the subject of experimental investigations and theoretical modeling. Here, we examine the possibility of accurately predicting the dynamics of the thin liquid film drainage using numerical simulations when compared to an experimental investigation of millimetric bubbles free-rising in pure water and colliding with a flat glass interface. A high-speed camera is used to track the bubble bounce trajectory, and a second high-speed camera together with a pulsed laser is used for interferometric determination of the shape and evolution of the thin liquid film profile during the bounce.

Free-Rising Bubbles Bounce More Strongly from Mobile than from Immobile Water-Air Interfaces.

Recently it was reported that the interface mobility of bubbles and emulsion droplets can have a dramatic effect not only on the characteristic coalescence times but also on the way that bubbles and droplets bounce back after collision (Vakarelski, I. U.; Yang, F.

Mobile-surface bubbles and droplets coalesce faster but bounce stronger.

Enhancing the hydrodynamic interfacial mobility of bubbles and droplets in multiphase systems is expected to reduce the characteristic coalescence times and thereby affect the stability of gas or liquid emulsions that are of wide industrial and biological importance. However, by comparing the controlled collision of bubbles or water droplets with mobile or immobile liquid interfaces, in a pure fluorocarbon liquid, we demonstrate that collisions involving mobile surfaces result in a significantly stronger series of rebounds before the rapid coalescence event. The stronger rebound is explained by the lower viscous dissipation during collisions involving mobile surfaces.

Stable-streamlined cavities following the impact of non-superhydrophobic spheres on water.

The formation of a stable-streamlined gas cavity following the impact of a heated Leidenfrost sphere on a liquid surface or a superhydrophobic sphere on water is a recently demonstrated phenomenon. A sphere encapsulated in a teardrop-shaped gas cavity was found to have near-zero hydrodynamic drag due to the self-adjusting streamlined shape and the free-slip boundary condition on the cavity interface. Here we show that such cavities can as well be formed following water impact from a sufficient height of non-superhydrophobic spheres with water contact angles between >30° and 120°.

The air entrapment under a drop impacting on a nano-rough surface.

We study the impact of drops onto a flat surface with a nano-particle-based superhydrophobic coating, focusing on the earliest contact using 200 ns time-resolution. A central air-disc is entrapped when the drop impacts the surface, and when the roughness is appropriately accounted for, the height and radial extent of the air-disc follow the scaling laws established for impacts onto smooth surfaces. The roughness also modifies the first contact of the drop around the central air-disc, producing a thick band of micro-bubbles.

Drag crisis moderation by thin air layers sustained on superhydrophobic spheres falling in water.

We investigate the effect of thin air layers naturally sustained on superhydrophobic surfaces on the terminal velocity and drag force of metallic spheres free falling in water. The surface of 20 mm to 60 mm steel or tungsten-carbide spheres is rendered superhydrophobic by a simple coating process that uses a commercially available hydrophobic agent. By comparing the free fall of unmodified spheres and superhydrophobic spheres in a 2.

Coalescence Dynamics of Mobile and Immobile Fluid Interfaces.

Coalescence dynamics between deformable bubbles and droplets can be dramatically affected by the mobility of the interfaces with fully tangentially mobile bubble-liquid or droplet-liquid interfaces expected to accelerate the coalescence by orders of magnitude. However, there is a lack of systematic experimental investigations that quantify this effect. By using high speed camera imaging we examine the free rise and coalescence of small air-bubbles (100 to 1300 μm in diameter) with a liquid interface.

Self-determined shapes and velocities of giant near-zero drag gas cavities.

Minimizing the retarding force on a solid moving in liquid is the canonical problem in the quest for energy saving by friction and drag reduction. For an ideal object that cannot sustain any shear stress on its surface, theory predicts that drag force will fall to zero as its speed becomes large. However, experimental verification of this prediction has been challenging.

Evaporative Lithography in Open Microfluidic Channel Networks.

We demonstrate a direct capillary-driven method based on wetting and evaporation of various suspensions to fabricate regular two-dimensional wires in an open microfluidic channel through continuous deposition of micro- or nanoparticles under evaporative lithography, akin to the coffee-ring effect. The suspension is gently placed in a loading reservoir connected to the main open microchannel groove on a PDMS substrate. Hydrophilic conditions ensure rapid spreading of the suspension from the loading reservoir to fill the entire channel length.

Leidenfrost Vapor Layers Reduce Drag without the Crisis in High Viscosity Liquids.

The drag coefficient C_{D} of a solid smooth sphere moving in a fluid is known to be only a function of the Reynolds number Re and diminishes rapidly at the drag crisis around Re∼3×10^{5}. A Leidenfrost vapor layer on a hot sphere surface can trigger the onset of the drag crisis at a lower Re. By using a range of high viscosity perfluorocarbon liquids, we show that the drag reduction effect can occur over a wide range of Re, from as low as ∼600 to 10^{5}.

Drag Moderation by the Melting of an Ice Surface in Contact with Water.

We report measurements of the effects of a melting ice surface on the hydrodynamic drag of ice-shell-metal-core spheres free falling in water at a Reynolds of number Re~2×10^{4}-3×10^{5} and demonstrate that the melting surface induces the early onset of the drag crisis, thus reducing the hydrodynamic drag by more than 50%. Direct visualization of the flow pattern demonstrates the key role of surface melting. Our observations support the hypothesis that the drag reduction is due to the disturbance of the viscous boundary layer by the mass transfer from the melting ice surface.

Leidenfrost vapour layer moderation of the drag crisis and trajectories of superhydrophobic and hydrophilic spheres falling in water.

We investigate the dynamic effects of a Leidenfrost vapour layer sustained on the surface of heated steel spheres during free fall in water. We find that a stable vapour layer sustained on the textured superhydrophobic surface of spheres falling through 95 °C water can reduce the hydrodynamic drag by up to 75% and stabilize the sphere trajectory for the Reynolds number between 10(4) and 10(6), spanning the drag crisis in the absence of the vapour layer. For hydrophilic spheres under the same conditions, the transition to drag reduction and trajectory stability occurs abruptly at a temperature different from the static Leidenfrost point.

Stabilization of thin liquid films by repulsive van der Waals force.

Using high-speed video recording of bubble rise experiments, we study the stability of thin liquid films trapped between a rising bubble and a surfactant-free liquid-liquid meniscus interface. Using different combinations of nonpolar oils and water that are all immiscible, we investigate the extent to which film stability can be predicted by attractive and repulsive van der Waals (vdW) interactions that are indicated by the relative magnitude of the refractive indices of the liquid combinations, for example, water (refractive index, n = 1.33), perfluorohexane (n = 1.

Dynamic air layer on textured superhydrophobic surfaces.

We provide an experimental demonstration that a novel macroscopic, dynamic continuous air layer or plastron can be sustained indefinitely on textured superhydrophobic surfaces in air-supersaturated water by a natural gas influx mechanism. This type of plastron is an intermediate state between Leidenfrost vapor layers on superheated surfaces and the equilibrium Cassie-Baxter wetting state on textured superhydrophobic surfaces. We show that such a plastron can be sustained on the surface of a centimeter-sized superhydrophobic sphere immersed in heated water and variations of its dynamic behavior with air saturation of the water can be regulated by rapid changes of the water temperature.

Foam-film-stabilized liquid bridge networks in evaporative lithography and wet granular matter.

Evaporative lithography using latex particle templates is a novel approach for the self-assembly of suspension-dispersed nanoparticles into ordered microwire networks. The phenomenon that drives the self-assembly process is the propagation of a network of interconnected liquid bridges between the template particles and the underlying substrate. With the aid of video microscopy, we demonstrate that these liquid bridges are in fact the border zone between the underlying substrate and foam films vertical to the substrate, which are formed during the evaporation of the liquid from the suspension.

Ionic enhancement of silica surface nanowear in electrolyte solutions.

The nanoscale wear and friction of silica and silicon nitride surfaces in aqueous electrolyte solutions were investigated by using sharp atomic force microscope (AFM) cantilever tips coated with silicon nitride. Measurements were carried out in aqueous solutions of varying pH and in monovalent and divalent cation chloride and nitrate solutions. The silica surface was shown to wear strongly in solutions of high pH (≈11.

Stabilization of Leidenfrost vapour layer by textured superhydrophobic surfaces.

In 1756, Leidenfrost observed that water drops skittered on a sufficiently hot skillet, owing to levitation by an evaporative vapour film. Such films are stable only when the hot surface is above a critical temperature, and are a central phenomenon in boiling. In this so-called Leidenfrost regime, the low thermal conductivity of the vapour layer inhibits heat transfer between the hot surface and the liquid.

Drag reduction by Leidenfrost vapor layers.

We demonstrate and quantify a highly effective drag reduction technique that exploits the Leidenfrost effect to create a continuous and robust lubricating vapor layer on the surface of a heated solid sphere moving in a liquid. Using high-speed video, we show that such vapor layers can reduce the hydrodynamic drag by over 85%. These results appear to approach the ultimate limit of drag reduction possible by different methods based on gas-layer lubrication and can stimulate the development of related energy saving technologies.

Dynamic interactions between microbubbles in water.

The interaction between moving bubbles, vapor voids in liquid, can arguably represent the simplest dynamical system in continuum mechanics as only a liquid and its vapor phase are involved. Surprisingly, and perhaps because of the ephemeral nature of bubbles, there has been no direct measurement of the time-dependent force between colliding bubbles which probes the effects of surface deformations and hydrodynamic flow on length scales down to nanometers. Using ultrasonically generated microbubbles (approximately 100 microm size) that have been accurately positioned in an atomic force microscope, we have made direct measurements of the force between two bubbles in water under controlled collision conditions that are similar to Brownian particles in solution.

Tailoring silica nanotribology for CMP slurry optimization: Ca(2+) cation competition in C(12)TAB mediated lubrication.

Self-assembled surfactant structures at the solid/liquid interface have been shown to act as nanoparticulate dispersants and are capable of providing a highly effective, self-healing boundary lubrication layer in aqueous environments. However, in some cases in particular, chemical mechanical planarization (CMP) applications the lubrication imparted by self-assembled surfactant dispersants can be too strong, resulting in undesirably low levels of wear or friction disabling material removal. In the present investigation, the influence of calcium cation (Ca(2+)) addition on dodecyl trimethylammonium bromide (C(12)TAB) mediated lubrication of silica surfaces is examined via normal and lateral atomic force microscopy (AFM/LFM), benchtop polishing experiments and surface adsorption characterization methods.

Lateral hydrodynamic interactions between an emulsion droplet and a flat surface evaluated by frictional force microscopy.

We introduce a lateral atomic force microscopy (AFM) method to measure the hydrodynamic drag force acting on a microscopic emulsion droplet moving parallel to a flat surface. A tetradecane oil droplet formed in an aqueous solution of sodium dodecylsulfate was attached to a V-shaped atomic force microscopy cantilever, and lateral hydrodynamic interactions between the droplet and a flat glass surface were measured using a range of scanning velocities. The droplet was positioned either far from the oscillating surface or was pressed to the surface under a constant applied load.

Variations in the spatial distribution of sonoluminescing bubbles in the presence of an ionic surfactant and electrolyte.

It has been established that the addition of sodium dodecylsulfate (SDS) to water to a concentration of 1 mM increased the integrated sonoluminescence (SL) intensity to a maximum. Moreover, further increase in the SDS concentration to 10 mM decreased the SL intensity to a level comparable to that obtained for water. Photographic images of water and 10 mM SDS have revealed a localized distribution of SL bubbles near the liquid surface.

Particulate templates and ordered liquid bridge networks in evaporative lithography.

We investigate the properties of latex particle templates required to optimize the development of ordered liquid bridge networks in evaporative lithography. These networks are key precursors in the assembly of solutions of conducting nanoparticles into large, optically transparent, and conducting microwire networks on substrates (Vakarelski, I. U.