اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدShear induced breakup of droplets in a colloidal dispersion
56
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We present numerical results for the breakup of a pair of colloidal particles enveloped by a droplet under shear flow. The smoothed profile method is used to accurately account for the hydrodynamic interactions between particles due to the host fluid. We observe that the critical capillary number, $Ca_{rm B}$, at which droplets breakup depends on a velocity ratio, $E$, defined as the ratio of the boundary shift velocity (that restores the droplet shape to a sphere) to the diffusive flux velocity in units of the particle radius $a$. For $E < 10$, $Ca_{B}$ is independent of $E$, as is consistent with the regime studied by Taylor. When $E > 10$, $Ca_{B}$ behaves as $Ca_{rm B} = 2E^{-1}$, which confirms Karam and Bellingers hypothesis. As a consequence, droplet break up will occur when the time scale of droplet deformation $dot{gamma}^{-1}$ is smaller than the diffusive time scale $t_{D} equiv a^{2}/Ltau$ in units of $a$, where $L$ is the diffusion constant and $tau$ is the 2nd order coefficient of the Ginzburg-Landau type free energy of the binary mixture. We emphasize that the breakup of droplet dispersed particles is not only governed by a balance of forces. We find that velocity competition is one of the important contributing factor.
قيم البحث
اقرأ أيضاً
Colloidal gels are formed through the aggregation of attractive particles, whose size ranges from 10~nm to a few micrometers, suspended in a liquid. Such gels are ubiquitous in everyday life applications, from food products to paints or construction
materials, in particular thanks to their ability to easily yield, i.e., to turn from a solid to a liquid under the application of a weak external load. Understanding and controlling the mechanical response of colloidal gels is therefore of prime importance. Depending on the details of the system, however, the resulting gel networks present different microstructural organisations that may lead to widely different mechanical responses. This raises important challenges in fully characterizing yielding and in uncovering the mechanisms of nonlinear response in colloidal gels. In this paper, we distinguish between two classes of colloidal gels showing respectively reversible yielding, where the gel network reforms upon load release, and irreversible yielding, where the network is fully destroyed through fractures and phase separation. This broad, empirical distinction is achieved through rheology and local experiments at a mesoscopic scale, intermediate between the network characteristic size and the sample size. We further discuss how the observables derived from creep and fatigue experiments may be modelled to predict yielding and highlight open questions and future research directions in the domain.
In directionally-dried colloidal dispersions regular bands can appear behind the drying front, inclined at $pm45^circ$ to the drying line. Although these features have been noted to share visual similarities to shear bands in metal, no physical mecha
nism for their formation has ever been suggested, until very recently. Here, through microscopy of silica and polystyrene dispersions, dried in Hele-Shaw cells, we demonstrate that the bands are indeed associated with local shear strains. We further show how the bands form, that they scale with the thickness of the drying layer, and that they are eliminated by the addition of salt to the drying dispersions. Finally, we reveal the origins of these bands in the compressive forces associated with drying, and show how they affect the optical properties (birefringence) of colloidal films and coatings.
Aqueous dispersion of Laponite, when exposed to carbon dioxide environment leads to in situ inducement of magnesium and lithium ions, which is, however absent when dispersion is exposed to air. Consequently, in the rheological experiments, Laponite d
ispersion preserved under carbon dioxide shows more spectacular enhancement in the elastic and viscous moduli as a function of time compared to that exposed to air. By measuring concentration of all the ions present in a dispersion as well as change in pH, the evolving inter-particle interactions among the Laponite particles is estimated. DLVO analysis of a limiting case is performed, wherein two particles approach each other in a parallel fashion a situation with maximum repulsive interactions. Interestingly it is observed that DLVO analysis explains the qualitative details of an evolution of elastic and viscous moduli remarkably well thereby successfully relating the macroscopic phenomena to the microscopic interactions.
Droplet-based microfluidics turned out to be an efficient and adjustable platform for digital analysis, encapsulation of cells, drug formulation, and polymerase chain reaction. Typically, for most biomedical applications, the handling of complex, non
-Newtonian fluids is involved, e.g. synovial and salivary fluids, collagen, and gel scaffolds. In this study we investigate the problem of droplet formation occurring in a microfluidic T-shaped junction, when the continuous phase is made of shear thinning liquids. At first, we review in detail the breakup process providing extensive, side-by-side comparisons between Newtonian and non-Newtonian liquids over unexplored ranges of flow conditions and viscous responses. The non-Newtonian liquid carrying the droplets is made of Xanthan solutions, a stiff rod-like polysaccharide displaying a marked shear thinning rheology. By defining an effective Capillary number, a simple yet effective methodology is used to account for the shear-dependent viscous response occurring at the breakup. The droplet size can be predicted over a wide range of flow conditions simply by knowing the rheology of the bulk continuous phase. Experimental results are complemented with numerical simulations of purely shear thinning fluids using Lattice Boltzmann models. The good agreement between the experimental and numerical data confirm the validity of the proposed rescaling with the effective Capillary number.
We examine microstructural and mechanical changes which occur during oscillatory shear flow and reformation after flow cessation of an intermediate volume fraction colloidal gel using rheometry and Brownian Dynamics (BD) simulations. A model depletio
n colloid-polymer mixture is used, comprising of a hard sphere colloidal suspension with the addition of non-adsorbing linear polymer chains. Results reveal three distinct regimes depending on the strain amplitude of oscillatory shear. Large shear strain amplitudes fully break the structure which results into a more homogenous and stronger gel after flow cessation. Intermediate strain amplitudes densify the clusters and lead to highly heterogeneous and weak gels. Shearing the gel to even lower strain amplitudes creates a less heterogonous stronger solid. These three regimes of shearing are connected to the microscopic shear-induced structural heterogeneity. A comparison with steady shear flow reveals that the latter does not produce structural heterogeneities as large as oscillatory shear. Therefore oscillatory shear is a much more efficient way of tuning the mechanical properties of colloidal gels. Moreover, colloidal gels presheared at large strain amplitudes exhibit a distinct nonlinear response characterized largely by a single yielding process while in those presheared at lower rates a two step yield process is promoted due to the creation of highly heterogeneous structures.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
