اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدCapillary attraction induced collapse of colloidal monolayers at fluid interfaces
97
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We investigate the evolution of a system of colloidal particles, trapped at a fluid interface and interacting via capillary attraction, as function of the range of the capillary interaction and temperature. We address the collapse of an initially homogeneous particle distribution and of a radially symmetric (disk--shaped) distribution of finite size, both theoretically by using a perturbative approach inspired by cosmological models and numerically by means of Brownian dynamics (BD) and dynamical density functional theory (DDFT). The results are summarized in a dynamical phase diagram, describing a smooth crossover from collective (gravitational-like) collapse to local (spinodal-like) clustering. In this crossover region, the evolution exhibits a peculiar shock wave behavior at the outer rim of the contracting, disk-shaped distribution.
قيم البحث
اقرأ أيضاً
Fluctuations of the interface between coexisting colloidal fluid phases have been measured with confocal microscopy. Due to a very low surface tension, the thermal motions of the interface are so slow, that a record can be made of the positions of th
e interface. The theory of the interfacial height fluctuations is developed. For a host of correlation functions, the experimental data are compared with the theoretical expressions. The agreement between theory and experiment is remarkably good.
Deformation of a fluid interface caused by the presence of objects at the interface can lead to large lateral forces between the objects. We explore these fluid-mediated attractive force between partially submerged vertical cylinders. Forces are expe
rimentally measured by slowly separating cylinder pairs and cylinder triplets after capillary rise is initially established for cylinders in contact. For cylinder pairs, numerical computations and a theoretical model are found to be in good agreement with measurements. The model provides insight into the relative importance of the contributions to the total force. For small separations, the pressure term dominates, while at large separations, surface tension becomes more important. A cross-over between the two regimes occurs at a separation of around half of a capillary length. The experimentally measured forces between cylinder triplets are also in good agreement with numerical computations, and we show that pair-wise contributions account for nearly all of the attractive force between triplets. For cylinders with equilibrium capillary rise height greater than the height of the cylinder, we find that the attractive force depends on the height of the cylinders above the submersion level, which provides a means to create precisely-controlled tunable cohesive forces between objects deforming a fluid interface.
The influence of a fluid-fluid interface on self-phoresis of chemically active, axially symmetric, spherical colloids is analyzed. Distinct from the studies of self-phoresis for colloids trapped at fluid interfaces or in the vicinity of hard walls, h
ere we focus on the issue of self-phoresis close to a fluid-fluid interface. In order to provide physically intuitive results highlighting the role played by the interface, the analysis is carried out for the case that the symmetry axis of the colloid is normal to the interface; moreover, thermal fluctuations are not taken into account. Similarly to what has been observed near hard walls, we find that such colloids can be set into motion even if their whole surface is homogeneously active. This is due to the anisotropy along the direction normal to the interface owing to the partitioning by diffusion, among the coexisting fluid phases, of the product of the chemical reaction taking place at the colloid surface. Different from results corresponding to hard walls, in the case of a fluid interface the direction of motion, i.e., towards the interface or away from it, can be controlled by tuning the physical properties of one of the two fluid phases. This effect is analyzed qualitatively and quantitatively, both by resorting to a far-field approximation and via an exact, analytical calculation which provides the means for a critical assessment of the approximate analysis.
The dynamics of active colloids is very sensitive to the presence of boundaries and interfaces which therefore can be used to control their motion. Here we analyze the dynamics of active colloids adsorbed at a fluid-fluid interface. By using a mesosc
opic numerical approach which relies on an approximated numerical solution of the Navier-Stokes equation, we show that when adsorbed at a fluid interface, an active colloid experiences a net torque even in the absence of a viscosity contrast between the two adjacent fluids. In particular, we study the dependence of this torque on the contact angle of the colloid with the fluid-fluid interface and on its surface properties. We rationalize our results via an approximate approach which accounts for the appearance of a local friction coefficient. By providing insight into the dynamics of active colloids adsorbed at fluid interfaces, our results are relevant for two-dimensional self assembly and emulsion stabilization by means of active colloids.
Euler buckling is the elastic instability of a column subjected to longitudinal compression forces at its ends. The buckling instability occurs when the compressing load reaches a critical value and an infinitesimal fluctuation leads to a large ampli
tude deflection. Since Eulers original study, this process has been extensively studied in homogeneous, isotropic, linear-elastic solids. Here, we examine the nature of the buckling in inhomogeneous soft composite materials. In particular, we consider a soft host with liquid inclusions both large and small relative to the elastocapillarity length, which lead to softening and stiffening of a homogeneous composite respectively. However, by imposing a gradient of the inclusion volume fraction or by varying the inclusion size we can deliberately manipulate the spatial structure of the composite properties of a column and thereby control the nature of Euler buckling.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
