Frozen autocatalytic fronts in a radial flow

Autocatalytic reaction-diffusion fronts are localized reaction zones propagating at a constant speed with a constant width. We show both theoretically and experimentally that, if the reactant <a:math xmlns:a="http://www.w3.org/1998/Math/MathML"><a:mi>Y</a:mi></a:math> of the autocatalytic reaction is injected radially at a constant flow rate in a sea of the autocatalytic species <b:math xmlns:b="http://www.w3.org/1998/Math/MathML"><b:mi>X</b:mi></b:math>, a stationary front can be maintained at a fixed position that scales linearly with the flow rate. When this reaction front is about to reach a stationary state, a second outward traveling front emerges to adapt the outer concentration of the autocatalytic species to the stoichiometry ratio between <c:math xmlns:c="http://www.w3.org/1998/Math/MathML"><c:mi>X</c:mi></c:math> and <d:math xmlns:d="http://www.w3.org/1998/Math/MathML"><d:mi>Y</d:mi></d:math>. Simple analytical solutions to the reaction-diffusion-advection equations governing the dynamics are computed for both fronts. The analytical predictions for the stationary front position and moving front dynamics as a function of injection flow rate, reactant concentration, and gap of the quasi-two-dimensional reactor agree well with experimental results obtained with the autocatalytic chlorite-tetrathionate reaction. Published by the American Physical Society 2024

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Publication Details

Journal
Physical Review Research
Published
2024-11-20
DOI
https://doi.org/10.1103/physrevresearch.6.l042044
Citations
4
Primary Topic
Spectroscopy and Quantum Chemical Studies
Type
article
Field-Weighted Citation Impact
1.35

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article

Frozen autocatalytic fronts in a radial flow

Luka Negrojević, A. De Wit, Fabian Brau, Alessandro Comolli
4 citations
Physical Review Research
Spectroscopy and Quantum Chemical Studies
1.35
article

Frozen autocatalytic fronts in a radial flow

Luka Negrojević, A. De Wit, Fabian Brau, Alessandro Comolli
article en
4 citations

Abstract

Autocatalytic reaction-diffusion fronts are localized reaction zones propagating at a constant speed with a constant width. We show both theoretically and experimentally that, if the reactant <a:math xmlns:a="http://www.w3.org/1998/Math/MathML"><a:mi>Y</a:mi></a:math> of the autocatalytic reaction is injected radially at a constant flow rate in a sea of the autocatalytic species <b:math xmlns:b="http://www.w3.org/1998/Math/MathML"><b:mi>X</b:mi></b:math>, a stationary front can be maintained at a fixed position that scales linearly with the flow rate. When this reaction front is about to reach a stationary state, a second outward traveling front emerges to adapt the outer concentration of the autocatalytic species to the stoichiometry ratio between <c:math xmlns:c="http://www.w3.org/1998/Math/MathML"><c:mi>X</c:mi></c:math> and <d:math xmlns:d="http://www.w3.org/1998/Math/MathML"><d:mi>Y</d:mi></d:math>. Simple analytical solutions to the reaction-diffusion-advection equations governing the dynamics are computed for both fronts. The analytical predictions for the stationary front position and moving front dynamics as a function of injection flow rate, reactant concentration, and gap of the quasi-two-dimensional reactor agree well with experimental results obtained with the autocatalytic chlorite-tetrathionate reaction. Published by the American Physical Society 2024

Physical Review ResearchVol. 6(4)
Université Libre de Bruxelles (BE)
European Commission, Horizon 2020, H2020 Marie Skłodowska-Curie Actions
Life below water
Openalex Percentile: Top 19%
Spectroscopy and Quantum Chemical Studies
1.35
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