اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدPhase behavior and rheology of sticky rod-like particles
141
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We construct colloidal ``sticky rods from the semi-flexible filamentous fd virus and temperature-sensitive polymers poly(N-isopropylacrylamide) (PNIPAM). The phase diagram of fd-PNIPAM system becomes independent of ionic strength at high salt concentration and low temperature, i.e. the rods are sterically stabilized by the polymer. However, the network of sticky rods undergoes a sol-gel transition as the temperature is raised. The viscoelastic moduli of fd and fd-PNIPAM suspensions are compared as a function of temperature, and the effect of ionic strength on the gelling behavior of fd-PNIPAM solution is measured. For all fluidlike and solidlike samples, the frequency-dependant linear viscoelastic moduli can be scaled onto universal master curves.
قيم البحث
اقرأ أيضاً
Lipid rafts are hypothesized to facilitate protein interaction, tension regulation, and trafficking in biological membranes, but the mechanisms responsible for their formation and maintenance are not clear. Insights into many other condensed matter p
henomena have come from colloidal systems, whose micron-scale particles mimic basic properties of atoms and molecules but permit dynamic visualization with single-particle resolution. Recently, experiments showed that bidisperse mixtures of filamentous viruses can self-assemble into colloidal monolayers with thermodynamically stable rafts exhibiting chiral structure and repulsive interactions. We quantitatively explain these observations by modeling the membrane particles as chiral liquid crystals. Chiral twist promotes the formation of finite-sized rafts and mediates a repulsion that distributes them evenly throughout the membrane. Although this system is composed of filamentous viruses whose aggregation is entropically driven by dextran depletants instead of phospholipids and cholesterol with prominent electrostatic interactions, colloidal and biological membranes share many of the same physical symmetries. Chiral twist can contribute to the behavior of both systems and may account for certain stereospecific effects observed in molecular membranes.
The paper studies the modes of vibrations of a lattice with rod-like particles, in a continuum model where the sites of the lattice are the connections among strings and rigid rods. In these structures then, translational and rotational degrees of fr
eedom are strongly coupled. We will discuss in particular two-dimensional lattices with auxetic-like behaviour. Auxetics are materials with a negative Poisson elastic parameter, meaning that they have a lateral extension, instead to shrink, when they are stretched. We assume as auxetic-like two-dimensional structures, structures which do not collapse, when stretched in one of the in-plane directions. The presence of rigid rod-like particles in the lattice prevents the shrinking of the membrane. Complete bandgaps between acoustic and optical modes are observed in analogy with the behaviour of crystalline materials.
When non-adsorbing polymers are added to an isotropic suspension of rod-like colloids, the colloids effectively attract each other via depletion forces. We performed Monte Carlo simulations to study the phase diagram of such rod-polymer mixture. The
colloidal rods were modelled as hard spherocylinders; the polymers were described as spheres of the same diameter as the rods. The polymers may overlap with no energy cost, while overlap of polymers and rods is forbidden. Large amounts of depletant cause phase separation of the mixture. We estimated the phase boundaries of isotropic-isotropic coexistence both, in the bulk and in confinement. To determine the phase boundaries we applied the grand canonical ensemble using successive umbrella sampling [J. Chem. Phys. 120, 10925 (2004)], and we performed a finite-size scaling analysis to estimate the location of the critical point. The results are compared with predictions of the free volume theory developed by Lekkerkerker and Stroobants [Nuovo Cimento D 16, 949 (1994)]. We also give estimates for the interfacial tension between the coexisting isotropic phases and analyse its power-law behaviour on approach of the critical point.
We study the rheology of a soft particulate system where the inter-particle interactions are weakly attractive. Using extensive molecular dynamics simulations, we scan across a wide range of packing fractions ($phi$), attraction strengths ($u$) and i
mposed shear-rates ($dot{gamma}$). In striking contrast to repulsive systems, we find that at small shear-rates generically a fragile isostatic solid is formed even if we go to $phi ll phi_J$. Further, with increasing shear-rates, even at these low $phi$, non-monotonic flow curves occur which lead to the formation of persistent shear-bands in large enough systems. By tuning the damping parameter, we also show that inertia plays an important role in this process. Furthermore, we observe enhanced particle dynamics in the attraction-dominated regime as well as a pronounced anisotropy of velocity and diffusion constant, which we take as precursors to the formation of shear bands. At low enough $phi$, we also observe structural changes via the interplay of low shear-rates and attraction with the formation of micro-clusters and voids. Finally, we characterize the properties of the emergent shear bands and thereby, we find surprisingly small mobility of these bands, leading to prohibitely long time-scales and extensive history effects in ramping experiments.
The rheology of cohesive granular materials, under a constant pressure condition, is studied using molecular dynamics simulations. Depending on the shear rate, pressure, and interparticle cohesiveness, the system exhibits four distinctive phases: uni
form shear, oscillation, shear-banding, and clustering. The friction coefficient is found to increase with the inertial number, irrespective of the cohesiveness. The friction coefficient becomes larger for strong cohesion. This trend is explained by the anisotropies of the coordination number and angular distribution of the interparticle forces. In particular, we demonstrate that the second-nearest neighbors play a role in the rheology of cohesive systems.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
