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Formation of Liesegang patterns in the presence of an electric field

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 Added by Ioana Bena Dr.
 Publication date 2005
  fields Physics
and research's language is English




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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-Hilliard equation with a moving source term representing the reaction zone, and the electric field enters through its effects on the properties of the reaction zone. We employ our previous results [I. Bena, F. Coppex, M. Droz, and Z. Racz, J. Chem. Phys. {bf 122}, 024512 (2005)] on how the electric field changes both the motion of the front, as well as the amount of reaction product left behind the front, and our main conclusion is that the number of precipitation bands becomes finite in a finite electric field. The reason for the finiteness in case when the electric field drives the reagents towards the reaction zone is that the width of consecutive bands increases so that, beyond a distance $ell_+$, the precipitation is continuous (plug is formed). In case of an electric field of opposite polarity, the bands emerge in a finite interval $ell_-$, since the reaction product decreases with time and the conditions for phase separation cease to exist. We give estimates of $ell_{pm}$ in terms of measurable quantities and thus present an experimentally verifiable prediction of the Cahn-Hilliard equation with a moving source description of Liesegang phenomena.



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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.
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