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We study the effects of irradiating water with 3 MeV protons at high doses by observing the motion of charged polystyrene beads outside the proton beam. By single-particle tracking, we measure a radial velocity of the order of microns per second. Combining electrokinetic theory with simulations of the beam-generated reaction products and their outward diffusion, we find that the bead motion is due to electrophoresis in the electric field induced by the mobility contrast of cations and anions. This work sheds light on the perturbation of biological systems by high-dose radiations and paves the way for the manipulation of colloid or macromolecular dispersions by radiation-induced diffusiophoresis.
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We report measurements of resonant thermal capillary oscillations of a hemispherical liquid gas interface obtained using a half bubble deposited on a solid substrate. The thermal motion of the hemispherical interface is investigated using an atomic force microscope cantilever that probes the amplitude of vibrations of this interface versus frequency. The spectrum of such nanoscale thermal oscillations of the bubble surface presents several resonance peaks and reveals that the contact line of the hemispherical bubble is pinned on the substrate. The analysis of these peaks allows us to measure the surface viscosity of the bubble interface. Minute amounts of impurities are responsible for altering the rheology of the pure water surface.
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We present a study of the hydrodynamics of an active particle-a model squirmer-in an environment with a broken rotational symmetry: a nematic liquid crystal. By combining simulations with analytic calculations, we show that the hydrodynamic coupling between the squirmer flow field and liquid crystalline director can lead to reorientation of the swimmers. The preferred orientation depends on the exact details of the squirmer flow field. In a steady state, pushers are shown to swim parallel with the nematic director while pullers swim perpendicular to the nematic director. This behavior arises solely from hydrodynamic coupling between the squirmer flow field and anisotropic viscosities of the host fluid. Our results suggest that an anisotropic swimming medium can be used to characterize and guide spherical microswimmers in the bulk.
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The "free" water surface is generally prone to contamination with surface impurities, be they surfactants, particles, or other surface active agents. The presence of such impurities can modify flow near such interfaces in a drastic manner. Here we show that vibrating a small sphere mounted on an atomic force microscope cantilever near a gas bubble immersed in water is an excellent probe of surface contamination. Both viscous and elastic forces are exerted by an air-water interface on the vibrating sphere even when very low doses of contaminants are present. The viscous drag forces show a crossover from no-slip to slip boundary conditions while the elastic forces show a nontrivial variation as the vibration frequency changes. We provide a simple model to rationalize these results and propose a simple way of evaluating the concentration of such surface impurities.
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A micrometer-sized spherical particle classically equilibrates at the water-air interface in partial wetting configuration, causing about no deformation to the interface. In condition of thermal equilibrium, the particle just undergoes faint Brownian motion, well visible under a microscope. We report experimental observations when the particle is made of a light-absorbing material and is heated up by a vertical laser beam. We show that, at small laser power, the particle is trapped in on-axis configuration, similarly to 2-dimensional trapping of a transparent sphere by optical forces. Conversely, on-axis trapping becomes unstable at higher power. The particle escapes off the laser axis and starts orbiting around the axis. We show that the laser-heated particle behaves as a microswimmer with velocities on the order of several 100 µm/s with just a few milliwatts of laser power.
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We study the thermophoretic coefficient D(T) of a charged colloid. The non-uniform electrolyte is characterized in terms of densities and diffusion currents of mobile ions. The hydrodynamic treatment in the vicinity of a solute particle relies on the Hückel approximation, which is valid for particles smaller than the Debye length, a << [Formula: see text] . To leading order in the parameter a/[Formula: see text] , we find that the coefficient D(T) consists of two contributions, a dielectrophoretic term proportional to the permittivity derivative dvarepsilon/dT , and a Seebeck term, i.e., the macroscopic electric field induced by the thermal gradient in the electrolyte solution. Depending on the particle valency, these terms may take opposite signs, and their temperature dependence may result in a change of sign of thermophoresis, as observed in several recent experiments.
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We study the electrostatic properties of charged particles trapped at an interface in a water-in-oil microemulsion. The electrostatic potential and the counterion distribution in the water droplet are given in terms of the ratio of the Debye screening length kappa(-1) and the droplet radius R. In the limit R-->infinity we recover the well-known results for a flat interface. Finite-size corrections are obtained in terms of the small parameter 1/kappaR. Part of the counterions spread along the interface and form a charged layer of one Debye length thickness. In particular, there is a uniform surface charge contribution. We derive explicit expressions for the electric field, the mobile charge density, and the charge-induced pressure on the interface.
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We study a simple model for an amphiphilic layer that may adsorb cosurfactant molecules from a reservoir. Upon varying the length of the cosurfactant, we obtain a discontinuous change of the adsorption rate and a corresponding discontinuity of the bending rigidity kappa. With realistic values for the chemical potential and the interaction energy of the hydrophobic tails, our model accounts quantitatively for the measured rigidity and the discontinuity observed for the ternary system AOT/water/oil and for SDS/alcohol bilayers.
Assuntos
Bicamadas Lipídicas/química , Modelos Biológicos , Modelos Químicos , Tensoativos/química , Adsorção , Elasticidade , Membranas Artificiais , Óleos/química , Dodecilsulfato de Sódio/química , Succinatos/metabolismo , Água/químicaRESUMO
We study the tail contributions to the elastic constants of an amphiphilic layer. For dense systems the terms arising from the attractive van der Waals interactions prevail, whereas the translational entropy of the liquid layer is essential at lower density. Both the membrane rigidity kappa and the Gaussian bending elastic constant kappa; strongly vary with the density of the hydrocarbon chains; for dense systems, they are of the order 100kT with a ratio kappa;/kappa = -2 / 3. At lower density, partial cancellation of interaction and entropic contributions leads to elastic constants of the order of kT, with a ratio close to the value -2 observed for microemulsions.