Self-propulsion of pure water droplets by spontaneous Marangoni stress driven motion

We report spontaneous motion in a fully bio-compatible system consisting of pure water droplets in an oil-surfactant medium of squalane and monoolein. Water from the droplet is solubilized by the reverse micellar solution, creating a concentration gradient of swollen reverse micelles around each droplet. The strong advection and weak diffusion conditions allow for the first experimental realization of spontaneous motion in a system of isotropic particles at sufficiently large P\'eclet number according to a straightforward generalization of a recently proposed mechanism. Experiments with a highly concentrated solution of salt instead of water, and tetradecane instead of squalane, confirm the above mechanism. The present swimming droplets are able to carry external bodies such as large colloids, salt crystals, and even cells.Comment: 5 pages, 5 figure

Realisation of the Brazil-nut effect in charged colloids without external driving

Sedimentation is a ubiquitous phenomenon across many fields of science, such as geology, astrophysics, and soft matter. Sometimes, sedimentation leads to unusual phenomena, such as the Brazil-nut effect, where heavier (granular) particles reside on top of lighter particles after shaking. We show experimentally that a Brazil-nut effect can be realised in a binary colloidal system of long-range repulsive charged particles driven purely by Brownian motion and electrostatics without the need for activity. Using theory, we argue that not only the mass-per-charge for the heavier particles needs to be smaller than the mass-per-charge for the lighter particles, but that at high overall density, the system can be trapped in a long-lived metastable state, which prevents the occurrence of the equilibrium Brazil-nut effect. Therefore, we envision that our work provides valuable insights into the physics of strongly interacting systems, such as partially glassy and crystalline structures. Finally, our theory, which quantitatively agrees with the experimental data, predicts that the shapes of sedimentation density profiles of multicomponent charged colloids are greatly altered when the particles are charge regulating with more than two ion species involved. Hence, we hypothesise that sedimentation experiments can aid in revealing the type of ion-adsorption processes that determine the particle charge and possibly the value of the corresponding equilibrium constants.Comment: 13 pages, 4 figures. In ancillary files: SI and 2 SI videos, published manuscript with improved explanation on quantification of parameter

О финансово-экономическом кризисе

У статті для визначення позиції молодих учених, стосовно фінансово-економічної кризи 2008–2010 р. використаний метод нечіткої кластеризації даних, що працює в режимі паралельної їхньої обробки. Наведено заходи щодо зниження наслідків кризи для України.В статье для определения позиции молодых ученых, применительно к финансово-экономическому кризису 2008—2010 гг. использован метод нечеткой кластеризации данных, который работает в режиме параллельной их обработки. Приведены мероприятия по снижению последствий кризиса для Украины.In an article for determining the position of young scientists, in relation to financial and economic crisis, 2008— 2010. used the method of fuzzy clustering, which operates in parallel processing. Shows the measures to reduce the impact of the crisis in Ukraine

Speed-Dispersion Induced Alignment : a 1D model inspired by swimming droplets experiments

We investigate the collective dynamics of self-propelled droplets, confined in a one dimensional micro-fluidic channel. On one hand, neighboring droplets align and form large trains of droplets moving in the same direction. On the other hand, the droplets condensates, leaving large regions with very low density. A careful examination of the interactions between two "colliding" droplets demonstrates that local alignment takes place as a result of the interplay between the dispersion of their speeds and the absence of Galilean invariance. Inspired by these observations, we propose a minimalistic 1D model of active particles reproducing such dynamical rules and, combining analytical arguments and numerical evidences, we show that the model exhibits a transition to collective motion in 1D for a large range of values of the control parameters. Condensation takes place as a transient phenomena which tremendously slows down the dynamics, before the system eventually settles into a homogeneous aligned phase.Comment: 5 pages, 5 figure

Formation of dodecagonal quasicrystals in two-dimensional systems of patchy particles

The behaviour of two-dimensional patchy particles with 5 and 7 regularly-arranged patches is investigated by computer simulation. For higher pressures and wider patch widths, hexagonal crystals have the lowest enthalpy, whereas at lower pressures and for narrower patches, lower-density crystals with five nearest neighbours and that are based on the (3^2,4,3,4) tiling of squares and triangles become lower in enthalpy. Interestingly, in regions of parameter space near to that where the hexagonal crystals become stable, quasicrystalline structures with dodecagonal symmetry form on cooling from high temperature. These quasicrystals can be considered as tilings of squares and triangles, and are probably stabilized by the large configurational entropy associated with all the different possible such tilings. The potential for experimentally realizing such structures using DNA multi-arm motifs are discussed.Comment: 12 pages, 12 figure

Realization of the Brazil-nut effect in charged colloids without external driving

Sedimentation is a ubiquitous phenomenon across many fields of science, such as geology, astrophysics, and soft matter. Sometimes, sedimentation leads to unusual phenomena, such as the Brazil-nut effect, where heavier (granular) particles reside on top of lighter particles after shaking. We show experimentally that a Brazil-nut effect can be realized in a binary colloidal system of long-range repulsive charged particles driven purely by Brownian motion and electrostatics without the need for activity. Using theory, we argue that not only the mass-per-charge for the heavier particles needs to be smaller than the mass-per-charge for the lighter particles but also that at high overall density, the system can be trapped in a long-lived metastable state, which prevents the occurrence of the equilibrium Brazil-nut effect. Therefore, we envision that our work provides valuable insights into the physics of strongly interacting systems, such as partially glassy and crystalline structures. Finally, our theory, which quantitatively agrees with the experimental data, predicts that the shapes of sedimentation density profiles of multicomponent charged colloids are greatly altered when the particles are charge-regulating with more than one ion species involved. Hence, we hypothesize that sedimentation experiments can aid in revealing the type of ion adsorption processes that determine the particle charge and possibly the value of the corresponding equilibrium constants

Evaporation of binary liquids from a capillary tube

Evaporation of multi-component liquid mixtures in confined geometries, such as capillaries, is crucial in applications such as microfluidics, two-phase cooling devices, and inkjet printing. Predicting the behaviour of such systems becomes challenging because evaporation triggers complex spatio-temporal changes in the composition of the mixture. These changes in composition, in turn, affect evaporation. In the present work, we study the evaporation of aqueous glycerol solutions contained as a liquid column in a capillary tube. Experiments and direct numerical simulations show three evaporation regimes characterised by different temporal evolutions of the normalised mass transfer rate (or Sherwood number, $Sh$), namely $Sh (\tilde{t}) = 1$, $Sh \sim 1/\sqrt{\tilde{t}}$, and $Sh \sim \exp\left(-\tilde{t}\right)$. Here $\tilde{t}$ is a normalised time. We present a simplistic analytical model which shows that the evaporation dynamics can be expressed by the classical relation $Sh = \exp \left( \tilde{t} \right) \mathrm{erfc} \left( \sqrt{\tilde{t}}\right)$. For small and medium $\tilde{t}$, this expression results in the first and second of the three observed scaling regimes, respectively. This analytical model is formulated in the limit of pure diffusion and when the penetration depth $\delta(t)$ of the diffusion front is much smaller than the length $L(t)$ of the liquid column. When $\delta \approx L$, finite length effects lead to $Sh \sim \exp\left(-\tilde{t}\right)$, i.e. the third regime. Finally, we extend our analytical model to incorporate the effect of advection and determine the conditions under which this effect is important. Our results provide fundamental insight into the physics of selective evaporation from a multi-component liquid column

Mathematical modeling for 1,6-hexanediol diacrylate photopolymerization in presence of oxygen

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