اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدCoalescence of Drops Near A Hydrophilic Boundary Leads to Long Range Directed Motion
113
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
A new mechanism for the passive removal of drop on a horizontal surface is described that does not require pre-fabrication of a surface energy gradient. The method relies upon the preparation of alternate hydrophilic/hydrophobic stripes on a surface. When one side of this surface is exposed to steam, with its other surface convectively cooled with cold water, steam condenses as a continuous film on the hydrophilic stripes but as droplets on the hydrophobic stripes. Coalescence leads to a random motion of the center of mass of the fused drops on the surface, which are readily removed as they reach near the boundary of the hydrophobic and hydrophilic zones thus resulting in a net diffusive flux of the coalesced drops from the hydrophobic to the hydrophilic stripes of the surface. Although an in-situ produced thermal gradient due to differential heat transfer coefficients of the hydrophilic and hydrophobic stripes could provide additional driving force for such a motion, it is, however, not a necessary condition for motion to occur. This method of creating directed motion of drops does not require a pre-existing wettability gradient and may have useful applications in thermal management devices.
قيم البحث
اقرأ أيضاً
It is well known that in Anderson localized systems, starting from a random product state the entanglement entropy remains bounded at all times. However, we show that adding a single boundary term to an otherwise Anderson localized Hamiltonian leads
to unbounded growth of entanglement. Our results imply that Anderson localization is not a local property. One cannot conclude that a subsystem has Anderson localized behavior without looking at the whole system, as a term that is arbitrarily far from the subsystem can affect the dynamics of the subsystem in such a way that the features of Anderson localization are lost.
We consider a model for periodic patterns of charges constrained over a cylindrical surface. In particular we focus on patterns of chiral helices, achiral rings or vertical lamellae, with the constraint of global electroneutrality. We study the depen
dence of the patterns size and pitch angle on the radius of the cylinder and salt concentration. We obtain a phase diagram by using numerical and analytic techniques. For pure Coulomb interactions, we find a ring phase for small radii and a chiral helical phase for large radii. At a critical salt concentration, the characteristic domain size diverges, resulting in macroscopic phase segregation of the components and restoring chiral symmetry. We discuss possible consequences and generalizations of our model.
We derive exact results for displacement fields that develop as a response to external pinning forces in two dimensional athermal networks. For a triangular lattice arrangement of particles interacting through soft potentials, we develop a Greens fun
ction formalism which we use to derive exact results for displacement fields produced by localized external forces. We show that in the continuum limit the displacement fields decay as $1/r$ at large distances $r$ away from a force dipole. Finally, we extend our formulation to study correlations in the displacement fields produced by the external pinning forces. We show that uncorrelated pinned forces at each vertex give rise to long-range correlations in displacements in athermal systems, with a non-trivial system size dependence. We verify our predictions with numerical simulations of athermal networks in two dimensions.
We introduce and study in two dimensions a new class of dry, aligning, active matter that exhibits a direct transition to orientational order, without the phase-separation phenomenology usually observed in this context. Characterized by self-propelle
d particles with velocity reversals and ferromagnetic alignment of polarities, systems in this class display quasi-long-range polar order with continuously-varying scaling exponents and yet a numerical study of the transition leads to conclude that it does not belong to the Berezinskii-Kosterlitz-Thouless universality class, but is best described as a standard critical point with algebraic divergence of correlations. We rationalize these findings by showing that the interplay between order and density changes the role of defects.
We study the stochastic dynamics of an electrolyte driven by a uniform external electric field and show that it exhibits generic scale invariance despite the presence of Debye screening. The resulting long-range correlations give rise to a Casimir-li
ke fluctuation-induced force between neutral boundaries that confine the ions; this force is controlled by the external electric field, and it can be both attractive and repulsive with similar boundary conditions, unlike other long-range fluctuation-induced forces. This work highlights the importance of nonequilibrium correlations in electrolytes and shows how they can be used to tune interactions between uncharged biological or synthetic structures at large separations.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
