Search arXiv⌕ Search
Home/Archive/arXiv

arXiv · cond-mat/0109068

Lamellar phase stability in diblock copolymers under reciprocating shear flows

Peilong Chen·Jorge Vinals
View original source ↗Read source document ↗Export metadata ↓

Abstract

A mesoscopic model of a diblock copolymer is used to study the stability of a uniform lamellar phase under a reciprocating shear flow. Approximate viscosity contrast between the microphases is allowed through a linear dependence of the (Newtonian) shear viscosity on monomer composition. We first show that viscosity contrast does not affect the composition of the base lamellar phase in an unbounded geometry, and that it only couples weakly to long wavelength perturbations. A perturbative analysis is then presented to address the stability of uniform lamellar structures under long wavelength perturbations by self-consistently solving for the composition and velocity fields of the perturbations. Stability boundaries are obtained as functions of the physical parameters of the polymer, the parameters of the flow and the initial orientation of the lamellae. We find that all orientations are linearly stable within specific ranges of parameters, but that the perpendicular orientation is generally stable within a larger range than the parallel orientation. Secondary instabilities are both of the Eckhaus type (longitudinal) and zig-zag type (transverse). The former is not expected to lead to re-orientation of the lamella, whereas in the second case the critical wavenumber is typically found to be along the perpendicular orientation.

Explore related subjects

cond-mat.softnlin.PS

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Peilong Chen, Jorge Vinals. 2001-09-04. Lamellar phase stability in diblock copolymers under reciprocating shear flows. https://doi.org/10.1021/ma011586s

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

arXiv2026

Speed up of passive tracers in mixtures with active chemical reactions

Diffusivity of passive tracers in complex mixtures is widely relevant for industrial applications and for probing biological systems. Interactions with the surrounding medium typically generate a drag force that suppresses tracer diffusion, although self-propulsion can accelerate tracers via active fluctuations. Similar effects are not understood in mixtures with particle conversion and exchange, although these are particularly relevant in biological contexts, where actively driven reactions prevail. By studying a thermodynamically consistent model of chemical reactions in mixtures, we show that reactions provide an additional relaxation pathway that suppresses interaction-induced memory, reducing the drag on tracers and restoring their diffusivity toward the value expected in the absence of solutes. Moreover, active reactions generate nonequilibrium fluctuations that can push tracer diffusivity beyond this limit, an effect we confirm with particle-based simulations. Our results identify chemical activity as a distinct route to controlling mass transport and offer a framework for interpreting microrheology experiments in chemically active mixtures.

cond-mat.soft↗
arXiv2026

Diffusion of charged rods across 3D varying section channels

We analyze the transport of rod-like particles by diffusion and drift in a three-dimensional channel with varying circular or elliptic cross section. Applying the Fick-Jacobs approximation to the transport equation of the particles' probability distribution, we derive an effective one-dimensional substitute model and the associated free energy profile. Our results show that the data for the mean first passage time of rods, once expressed as a function of the effective free energy barrier, collapse onto the same master curve as obtained for point or spherical particles. The observed universality provides a simple framework for predicting transport times of anisotropic particles in confined geometries without resolving the full multidimensional dynamics.

cond-mat.soft↗
arXiv2026

Reciprocal theorem for ion-releasing colloidal particles

We describe a generalization of the reciprocal theorem for particles suspended in electrolyte solutions and subjected to an electric field that could be either applied or emerged spontaneously. Attention is focused on catalytic colloids that release ions. The power of the generalization is to capture the effect of formation of a secondary cloud around a catalytic particle, which is equivalent to accounting for an excess charge $Q$ of a system. Our results show that the propulsion speed of catalytic particles has an extra contribution proportional to $Q$ and an external field $E_{\infty}$. The derived equation for $Q$ reveals that its sign is defined by the difference in the ion diffusivity and the magnitude is controlled by the average flux of ions from the surface. We demonstrate the application of the generalized theorem to electro- and diffusiophoresis of homogeneously releasing ions passive particles, as well as to a self-propulsion of inhomogeneous active particles (microswimmers). It is shown that whilst in some situations the extra term in the reciprocal theorem vanishes or has a little effect on the particle mobility, in many others it may dramatically change its magnitude, and even sign. In addition, the relevance of our results for microswimmer interactions is discussed briefly.

cond-mat.soft↗