Sulfur isotope fractionation during oxidation of sulfur dioxide: gas-phase oxidation by OH radicals and aqueous oxidation by H2O2, O3 and iron catalysis
Item
Title (Dublin Core)
Sulfur isotope fractionation during oxidation of sulfur dioxide: gas-phase oxidation by OH radicals and aqueous oxidation by H2O2, O3 and iron catalysis
Description (Dublin Core)
The oxidation of SO<sub>2</sub> to sulfate is a key reaction in determining the role of sulfate in the environment through its effect on aerosol size distribution and composition. Sulfur isotope analysis has been used to investigate sources and chemical processes of sulfur dioxide and sulfate in the atmosphere, however interpretation of measured sulfur isotope ratios is challenging due to a lack of reliable information on the isotopic fractionation involved in major transformation pathways. This paper presents laboratory measurements of the fractionation factors for the major atmospheric oxidation reactions for SO<sub>2</sub>: Gas-phase oxidation by OH radicals, and aqueous oxidation by H<sub>2</sub>O<sub>2</sub>, O<sub>3</sub> and a radical chain reaction initiated by iron. The measured fractionation factor for <sup>34</sup>S/<sup>32</sup>S during the gas-phase reaction is α<sub>OH</sub> = (1.0089±0.0007)−((4±5)×10<sup>−5</sup>) <i>T</i>(°C). The measured fractionation factor for <sup>34</sup>S/<sup>32</sup>S during aqueous oxidation by H<sub>2</sub>O<sub>2</sub> or O<sub>3</sub> is α<sub>aq</sub> = (1.0167±0.0019)−((8.7±3.5) ×10<sup>−5</sup>)<i>T</i>(°C). The observed fractionation during oxidation by H<sub>2</sub>O<sub>2</sub> and O<sub>3</sub> appeared to be controlled primarily by protonation and acid-base equilibria of S(IV) in solution, which is the reason that there is no significant difference between the fractionation produced by the two oxidants within the experimental error. The isotopic fractionation factor from a radical chain reaction in solution catalysed by iron is α<sub>Fe</sub> = (0.9894±0.0043) at 19 °C for <sup>34</sup>S/<sup>32</sup>S. Fractionation was mass-dependent with regards to <sup>33</sup>S/<sup>32</sup>S for all the reactions investigated. The radical chain reaction mechanism was the only measured reaction that had a faster rate for the light isotopes. The results presented in this study will be particularly useful to determine the importance of the transition metal-catalysed oxidation pathway compared to other oxidation pathways, but other main oxidation pathways can not be distinguished based on stable sulfur isotope measurements alone.
Creator (Dublin Core)
Harris, E.
Sinha, B.
Hoppe, P.
Crowley, J. N.
Ono, S.
Foley, S.
Date (Dublin Core)
2018-01-15
Type (Dublin Core)
Text
Format (Dublin Core)
application/pdf
Identifier (Dublin Core)
10.5194/acp-12-407-2012
https://acp.copernicus.org/articles/12/407/2012/
Source (Dublin Core)
eISSN: 1680-7324
Language (Dublin Core)
eng
