Photocatalytic chloride-to-chlorine conversion by ionic iron in aqueous aerosols: a combined experimental, quantum chemical, and chemical equilibrium model study

<p>Prior aerosol chamber experiments show that the ligand-to-metal charge transfer absorption in iron(III) chlorides can lead to the production of chlorine (Cl<span class="inline-formula"><sub>2</sub></span>/Cl). Based on this mechanism, the photocatalytic oxi...

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Main Authors: M. K. Mikkelsen, J. B. Liisberg, M. M. J. W. van Herpen, K. V. Mikkelsen, M. S. Johnson
Format: Article
Language:English
Published: Copernicus Publications 2024-03-01
Series:Aerosol Research
Online Access:https://ar.copernicus.org/articles/2/31/2024/ar-2-31-2024.pdf
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author M. K. Mikkelsen
J. B. Liisberg
M. M. J. W. van Herpen
K. V. Mikkelsen
M. S. Johnson
author_facet M. K. Mikkelsen
J. B. Liisberg
M. M. J. W. van Herpen
K. V. Mikkelsen
M. S. Johnson
author_sort M. K. Mikkelsen
collection DOAJ
description <p>Prior aerosol chamber experiments show that the ligand-to-metal charge transfer absorption in iron(III) chlorides can lead to the production of chlorine (Cl<span class="inline-formula"><sub>2</sub></span>/Cl). Based on this mechanism, the photocatalytic oxidation of chloride (Cl<span class="inline-formula"><sup>−</sup></span>) in mineral dust–sea spray aerosols was recently shown to be the largest source of chlorine over the North Atlantic. However, there has not been a detailed analysis of the mechanism that includes the aqueous formation equilibria and the absorption spectra of the iron chlorides nor has there been an analysis of which iron chloride is the main chromophore. Here we present the results of experiments measuring the photolysis of FeCl<span class="inline-formula"><sub>3</sub></span> <span class="inline-formula">⋅</span> 6H<span class="inline-formula"><sub>2</sub></span>O in specific wavelength bands, an analysis of the absorption spectra of FeCl<span class="inline-formula"><math xmlns="http://www.w3.org/1998/Math/MathML" id="M6" display="inline" overflow="scroll" dspmath="mathml"><mrow><msubsup><mi/><mi>n</mi><mrow><mn mathvariant="normal">3</mn><mo>-</mo><mi>n</mi></mrow></msubsup></mrow></math><span><svg:svg xmlns:svg="http://www.w3.org/2000/svg" width="17pt" height="16pt" class="svg-formula" dspmath="mathimg" md5hash="fb86d1cea1d2072e93be953ab610af6f"><svg:image xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="ar-2-31-2024-ie00001.svg" width="17pt" height="16pt" src="ar-2-31-2024-ie00001.png"/></svg:svg></span></span> (<span class="inline-formula"><i>n</i>=1</span> … 4) made using density functional theory, and the results of an aqueous-phase model that predicts the abundance of the iron chlorides with changes in pH and iron concentrations. Transition state analysis is used to determine the energy thresholds of the dissociations of the species. Based on a speciation model with conditions extending from dilute water droplets and acidic seawater droplets to brine and salty crust, as well as the absorption rates and dissociation thresholds, we find that FeCl<span class="inline-formula"><math xmlns="http://www.w3.org/1998/Math/MathML" id="M8" display="inline" overflow="scroll" dspmath="mathml"><mrow><msubsup><mi/><mn mathvariant="normal">2</mn><mo>+</mo></msubsup></mrow></math><span><svg:svg xmlns:svg="http://www.w3.org/2000/svg" width="8pt" height="15pt" class="svg-formula" dspmath="mathimg" md5hash="a685953c08dd2ff7fc811710de5bbda3"><svg:image xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="ar-2-31-2024-ie00002.svg" width="8pt" height="15pt" src="ar-2-31-2024-ie00002.png"/></svg:svg></span></span> is the most important species for chlorine production for a wide range of conditions. The mechanism was found to be active in the range of 400 to 530 nm, with a maximum around 440 nm. We conclude that iron chlorides will form in atmospheric aerosols from the combination of iron(III) cations with chloride and that they will be activated by sunlight, generating chlorine (Cl<span class="inline-formula"><sub>2</sub></span>/Cl) from chloride (Cl<span class="inline-formula"><sup>−</sup></span>) in a process that is catalytic in both chlorine and iron.</p>
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spelling doaj-art-3e8a343487a64aa4a96132203b5378de2025-08-20T02:22:37ZengCopernicus PublicationsAerosol Research2940-33912024-03-012314710.5194/ar-2-31-2024Photocatalytic chloride-to-chlorine conversion by ionic iron in aqueous aerosols: a combined experimental, quantum chemical, and chemical equilibrium model studyM. K. Mikkelsen0J. B. Liisberg1M. M. J. W. van Herpen2K. V. Mikkelsen3M. S. Johnson4Department of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen Ø, DenmarkDepartment of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen Ø, DenmarkAcacia Impact Innovation, Maarten van Herpen, Bernheze 5384 BB, the NetherlandsDepartment of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen Ø, DenmarkDepartment of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen Ø, Denmark<p>Prior aerosol chamber experiments show that the ligand-to-metal charge transfer absorption in iron(III) chlorides can lead to the production of chlorine (Cl<span class="inline-formula"><sub>2</sub></span>/Cl). Based on this mechanism, the photocatalytic oxidation of chloride (Cl<span class="inline-formula"><sup>−</sup></span>) in mineral dust–sea spray aerosols was recently shown to be the largest source of chlorine over the North Atlantic. However, there has not been a detailed analysis of the mechanism that includes the aqueous formation equilibria and the absorption spectra of the iron chlorides nor has there been an analysis of which iron chloride is the main chromophore. Here we present the results of experiments measuring the photolysis of FeCl<span class="inline-formula"><sub>3</sub></span> <span class="inline-formula">⋅</span> 6H<span class="inline-formula"><sub>2</sub></span>O in specific wavelength bands, an analysis of the absorption spectra of FeCl<span class="inline-formula"><math xmlns="http://www.w3.org/1998/Math/MathML" id="M6" display="inline" overflow="scroll" dspmath="mathml"><mrow><msubsup><mi/><mi>n</mi><mrow><mn mathvariant="normal">3</mn><mo>-</mo><mi>n</mi></mrow></msubsup></mrow></math><span><svg:svg xmlns:svg="http://www.w3.org/2000/svg" width="17pt" height="16pt" class="svg-formula" dspmath="mathimg" md5hash="fb86d1cea1d2072e93be953ab610af6f"><svg:image xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="ar-2-31-2024-ie00001.svg" width="17pt" height="16pt" src="ar-2-31-2024-ie00001.png"/></svg:svg></span></span> (<span class="inline-formula"><i>n</i>=1</span> … 4) made using density functional theory, and the results of an aqueous-phase model that predicts the abundance of the iron chlorides with changes in pH and iron concentrations. Transition state analysis is used to determine the energy thresholds of the dissociations of the species. Based on a speciation model with conditions extending from dilute water droplets and acidic seawater droplets to brine and salty crust, as well as the absorption rates and dissociation thresholds, we find that FeCl<span class="inline-formula"><math xmlns="http://www.w3.org/1998/Math/MathML" id="M8" display="inline" overflow="scroll" dspmath="mathml"><mrow><msubsup><mi/><mn mathvariant="normal">2</mn><mo>+</mo></msubsup></mrow></math><span><svg:svg xmlns:svg="http://www.w3.org/2000/svg" width="8pt" height="15pt" class="svg-formula" dspmath="mathimg" md5hash="a685953c08dd2ff7fc811710de5bbda3"><svg:image xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="ar-2-31-2024-ie00002.svg" width="8pt" height="15pt" src="ar-2-31-2024-ie00002.png"/></svg:svg></span></span> is the most important species for chlorine production for a wide range of conditions. The mechanism was found to be active in the range of 400 to 530 nm, with a maximum around 440 nm. We conclude that iron chlorides will form in atmospheric aerosols from the combination of iron(III) cations with chloride and that they will be activated by sunlight, generating chlorine (Cl<span class="inline-formula"><sub>2</sub></span>/Cl) from chloride (Cl<span class="inline-formula"><sup>−</sup></span>) in a process that is catalytic in both chlorine and iron.</p>https://ar.copernicus.org/articles/2/31/2024/ar-2-31-2024.pdf
spellingShingle M. K. Mikkelsen
J. B. Liisberg
M. M. J. W. van Herpen
K. V. Mikkelsen
M. S. Johnson
Photocatalytic chloride-to-chlorine conversion by ionic iron in aqueous aerosols: a combined experimental, quantum chemical, and chemical equilibrium model study
Aerosol Research
title Photocatalytic chloride-to-chlorine conversion by ionic iron in aqueous aerosols: a combined experimental, quantum chemical, and chemical equilibrium model study
title_full Photocatalytic chloride-to-chlorine conversion by ionic iron in aqueous aerosols: a combined experimental, quantum chemical, and chemical equilibrium model study
title_fullStr Photocatalytic chloride-to-chlorine conversion by ionic iron in aqueous aerosols: a combined experimental, quantum chemical, and chemical equilibrium model study
title_full_unstemmed Photocatalytic chloride-to-chlorine conversion by ionic iron in aqueous aerosols: a combined experimental, quantum chemical, and chemical equilibrium model study
title_short Photocatalytic chloride-to-chlorine conversion by ionic iron in aqueous aerosols: a combined experimental, quantum chemical, and chemical equilibrium model study
title_sort photocatalytic chloride to chlorine conversion by ionic iron in aqueous aerosols a combined experimental quantum chemical and chemical equilibrium model study
url https://ar.copernicus.org/articles/2/31/2024/ar-2-31-2024.pdf
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