Microphysics of the aqueous bulk counters the water activity driven rate acceleration of bromide oxidation by ozone from 289-245 K

The reaction of ozone with bromide is an initiation process in bromine activation resulting in the formation of reactive bromine species with impacts on the fate of compounds in the lower atmosphere. Environmental halide sources often contain organics, which are known to influence aqueous bulk react...

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Main Authors: Edebeli, Jacinta, Ammann, Markus, Bartels-Rausch, Thorsten
Format: Text
Language:English
Published: ETH Zurich 2019
Subjects:
Online Access:https://dx.doi.org/10.3929/ethz-b-000322290
http://hdl.handle.net/20.500.11850/322290
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spelling ftdatacite:10.3929/ethz-b-000322290 2023-05-15T18:18:54+02:00 Microphysics of the aqueous bulk counters the water activity driven rate acceleration of bromide oxidation by ozone from 289-245 K Edebeli, Jacinta Ammann, Markus Bartels-Rausch, Thorsten 2019 application/pdf https://dx.doi.org/10.3929/ethz-b-000322290 http://hdl.handle.net/20.500.11850/322290 en eng ETH Zurich info:eu-repo/semantics/openAccess Creative Commons Attribution Non Commercial 3.0 Unported https://creativecommons.org/licenses/by-nc/3.0/legalcode cc-by-nc-3.0 CC-BY-NC Text article-journal Journal Article ScholarlyArticle 2019 ftdatacite https://doi.org/10.3929/ethz-b-000322290 2021-11-05T12:55:41Z The reaction of ozone with bromide is an initiation process in bromine activation resulting in the formation of reactive bromine species with impacts on the fate of compounds in the lower atmosphere. Environmental halide sources often contain organics, which are known to influence aqueous bulk reactivity. Here, we present a study investigating the temperature dependence of bromide oxidation by ozone using a coated wall flow tube reactor coated with an aqueous mixture of citric acid, as a proxy for oxidized secondary organic matter, and sodium bromide. Using the resistor model formulation, we quantify changes in the properties of the aqueous bulk relevant for the observed reactivity. The reactive uptake coefficient decreased from 2 × 10−6 at 289 K to 0.5 × 10−6 at 245 K. Our analysis indicates that the humidity-driven increase in concentration with a corresponding increase in the pseudo-first order reaction rate was countered by the colligative change in ozone solubility and the effect of the organic fraction via increased viscosity and decreased diffusivity of ozone as the temperature decreased. From our parameterization, we provide an extension of the temperature dependence of the reaction rate coefficients driving the oxidation of bromide, and assess the temperature-dependent salting effects of citric acid on ozone solubility. This study shows the effects of the organic species at relatively mild temperatures, between the freezing point and eutectic temperature of sea as is typical for the Earth's cryosphere. Thus, this study may be relevant for atmospheric models at different scales describing halogen activation in the marine boundary layer or free troposphere including matrices such as sea-spray aerosol and brine in sea ice, snow, and around mid-latitude salt lakes. : Environmental Science: Processes & Impacts, 21 (1) : ISSN:2050-7887 : ISSN:2050-7895 Text Sea ice DataCite Metadata Store (German National Library of Science and Technology)
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language English
description The reaction of ozone with bromide is an initiation process in bromine activation resulting in the formation of reactive bromine species with impacts on the fate of compounds in the lower atmosphere. Environmental halide sources often contain organics, which are known to influence aqueous bulk reactivity. Here, we present a study investigating the temperature dependence of bromide oxidation by ozone using a coated wall flow tube reactor coated with an aqueous mixture of citric acid, as a proxy for oxidized secondary organic matter, and sodium bromide. Using the resistor model formulation, we quantify changes in the properties of the aqueous bulk relevant for the observed reactivity. The reactive uptake coefficient decreased from 2 × 10−6 at 289 K to 0.5 × 10−6 at 245 K. Our analysis indicates that the humidity-driven increase in concentration with a corresponding increase in the pseudo-first order reaction rate was countered by the colligative change in ozone solubility and the effect of the organic fraction via increased viscosity and decreased diffusivity of ozone as the temperature decreased. From our parameterization, we provide an extension of the temperature dependence of the reaction rate coefficients driving the oxidation of bromide, and assess the temperature-dependent salting effects of citric acid on ozone solubility. This study shows the effects of the organic species at relatively mild temperatures, between the freezing point and eutectic temperature of sea as is typical for the Earth's cryosphere. Thus, this study may be relevant for atmospheric models at different scales describing halogen activation in the marine boundary layer or free troposphere including matrices such as sea-spray aerosol and brine in sea ice, snow, and around mid-latitude salt lakes. : Environmental Science: Processes & Impacts, 21 (1) : ISSN:2050-7887 : ISSN:2050-7895
format Text
author Edebeli, Jacinta
Ammann, Markus
Bartels-Rausch, Thorsten
spellingShingle Edebeli, Jacinta
Ammann, Markus
Bartels-Rausch, Thorsten
Microphysics of the aqueous bulk counters the water activity driven rate acceleration of bromide oxidation by ozone from 289-245 K
author_facet Edebeli, Jacinta
Ammann, Markus
Bartels-Rausch, Thorsten
author_sort Edebeli, Jacinta
title Microphysics of the aqueous bulk counters the water activity driven rate acceleration of bromide oxidation by ozone from 289-245 K
title_short Microphysics of the aqueous bulk counters the water activity driven rate acceleration of bromide oxidation by ozone from 289-245 K
title_full Microphysics of the aqueous bulk counters the water activity driven rate acceleration of bromide oxidation by ozone from 289-245 K
title_fullStr Microphysics of the aqueous bulk counters the water activity driven rate acceleration of bromide oxidation by ozone from 289-245 K
title_full_unstemmed Microphysics of the aqueous bulk counters the water activity driven rate acceleration of bromide oxidation by ozone from 289-245 K
title_sort microphysics of the aqueous bulk counters the water activity driven rate acceleration of bromide oxidation by ozone from 289-245 k
publisher ETH Zurich
publishDate 2019
url https://dx.doi.org/10.3929/ethz-b-000322290
http://hdl.handle.net/20.500.11850/322290
genre Sea ice
genre_facet Sea ice
op_rights info:eu-repo/semantics/openAccess
Creative Commons Attribution Non Commercial 3.0 Unported
https://creativecommons.org/licenses/by-nc/3.0/legalcode
cc-by-nc-3.0
op_rightsnorm CC-BY-NC
op_doi https://doi.org/10.3929/ethz-b-000322290
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