ﻻ يوجد ملخص باللغة العربية
We study the effects of an external electric field on both the motion of the reaction zone and the spatial distribution of the reaction product, $C$, in an irreversible $A^- +B^+ to C$ reaction-diffusion process. The electrolytes $Aequiv (A^+,A^-)$ and $Bequiv (B^+,B^-)$ are initially separated in space and the ion-dynamics is described by reaction-diffusion equations obeying local electroneutrality. Without an electric field, the reaction zone moves diffusively leaving behind a constant concentration of $C$-s. In the presence of an electric field which drives the reagents towards the reaction zone, we find that the reaction zone still moves diffusively but with a diffusion coefficient which slightly decreases with increasing field. The important electric field effect is that the concentration of $C$-s is no longer constant but increases linearly in the direction of the motion of the front. The case of an electric field of reversed polarity is also discussed and it is found that the motion of the front has a diffusive, as well as a drift component. The concentration of $C$-s decreases in the direction of the motion of the front, up to the complete extinction of the reaction. Possible applications of the above results to the understanding of the formation of Liesegang patterns in an electric field is briefly outlined.
Starting from a generic model of a pore/bulk mixture equilibrium, we propose a novel method for modulating the composition of the confined fluid without having to modify the bulk state. To achieve this, two basic mechanisms - sensitivity of the pore
Understanding how electrolyte solutions behave out of thermal equilibrium is a long-standing endeavor in many areas of chemistry and biology. Although mean-field theories are widely used to model the dynamics of electrolytes, it is also important to
The effects of an external electric field on the formation of Liesegang patterns are investigated. The patterns are assumed to emerge from a phase separation process in the wake of a diffusive reaction front. The dynamics is described by a Cahn-Hilli
We revisit the problem of pinning a reaction-diffusion front by a defect, in particular by a reaction-free region. Using collective variables for the front and numerical simulations, we compare the behaviors of a bistable and monostable front. A bist
The latest trend in studies of modern electronically and/or optically active materials is to provoke phase transformations induced by high electric fields or by short (femtosecond) powerful optical pulses. The systems of choice are cooperative electr