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Spatiotemporal Patterns and Nonclassical Kinetics of Competing Elementary Reactions:  Chromium Complex Formation with Xylenol Orange in a Capillary
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    Spatiotemporal Patterns and Nonclassical Kinetics of Competing Elementary Reactions:  Chromium Complex Formation with Xylenol Orange in a Capillary
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    Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109-1055, and Department of Physics, Bar-Ilan University, Ramat-Gan 52900, Israel
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    The Journal of Physical Chemistry A

    Cite this: J. Phys. Chem. A 1997, 101, 15, 2819–2827
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    https://doi.org/10.1021/jp962994e
    Published April 10, 1997
    Copyright © 1997 American Chemical Society

    Abstract

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    An experimental investigation of chemical reaction fronts, created by an initial separation of reactants, is reported for a system of two competing reactions. Spatiotemporal patterns are observed experimentally for the competing reaction front and are accounted for quantitatively by a reaction-diffusion model. We use the reaction of xylenol orange with Cr3+ in aqueous solution. Different oligomers of Cr3+ provide the two kinetically different species that react competitively with xylenol orange. The parameters that determine whether pattern formation is observable at the front are the ratios of (1) the microscopic reaction constants of the competing reactions and (2) the concentrations of the competing species. Under the parameter values studied, which allowed clear spatiotemporal separation of the two competing reactions, we find that the behavior of the reaction front at early times follows a perturbation theory developed for a simple elementary A + B → C reaction with initially separated reactants. The global reaction rate, observed over the entire time scale of the experiments, is highly non-monotonic. Overall, with no free parameters, our theoretical model is quantitatively consistent with the experimental observations of the spatiotemporal patterns, the unusual scaling laws, and the crossover behaviors. The geometrical constraints and nonclassical behavior of the reaction rate allow a quantitative determination of the reaction probability of the chromium ion monomer relative to that of the higher order oligomers.

    Copyright © 1997 American Chemical Society

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    University of Michigan.

     Present address:  Inorganic Division, Department of Chemistry, National Institute of Technology and Quality, 2 Chungang-dong, Kwachon, Kyounggido, Korea.

    §

     Bar-Ilan University.

    *

     Corresponding author.

     Abstract published in Advance ACS Abstracts, March 15, 1997.

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    This article is cited by 16 publications.

    1. Christophe Léger and, Françoise Argoul, , Martin Z. Bazant. Front Dynamics during Diffusion-Limited Corrosion of Ramified Electrodeposits. The Journal of Physical Chemistry B 1999, 103 (28) , 5841-5851. https://doi.org/10.1021/jp990486+
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    12. Misha Sinder, Joshua Pelleg. Asymptotic properties of a reversible A + B ↔ C (static) reaction-diffusion process with initially separated reactants. Physical Review E 2000, 62 (3) , 3340-3348. https://doi.org/10.1103/PhysRevE.62.3340
    13. Misha Sinder, Joshua Pelleg. Properties of the crossover from nonclassical to classical chemical kinetics in a reversible A + B ↔ C reaction diffusion process. Physical Review E 1999, 60 (6) , R6259-R6262. https://doi.org/10.1103/PhysRevE.60.R6259
    14. Alejandro D Sánchez, Horacio S Wio. Kinetics of coupled bimolecular diffusion-limited reactions. Physica A: Statistical Mechanics and its Applications 1999, 272 (3-4) , 429-449. https://doi.org/10.1016/S0378-4371(99)00224-1
    15. Sung Hyun Park, Haim Taitelbaum, Raoul Kopelman. Competing Elementary Reactions in a Capillary - Two Reaction Fronts Moving in Opposite Directions. MRS Proceedings 1998, 543 https://doi.org/10.1557/PROC-543-249
    16. Andrew Yen, Raoul Kopelman. Experimental study of a ternary A + 2 B → C reaction-diffusion system with a propagating reaction front: Scaling exponents. Physical Review E 1997, 56 (3) , 3694-3696. https://doi.org/10.1103/PhysRevE.56.3694

    The Journal of Physical Chemistry A

    Cite this: J. Phys. Chem. A 1997, 101, 15, 2819–2827
    Click to copy citationCitation copied!
    https://doi.org/10.1021/jp962994e
    Published April 10, 1997
    Copyright © 1997 American Chemical Society

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