Multiphase oxidation of SO<sub>2</sub> by NO<sub>2</sub> on CaCO<sub>3</sub> particles
Heterogeneous/multiphase oxidation of SO<sub>2</sub> by NO<sub>2</sub> on solid or aqueous particles is thought to be a potentially important source of sulfate in the atmosphere, for example, during heavily polluted episodes (haze), but the reaction mechanism and rate are...
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| Format: | Article |
| Language: | English |
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Copernicus Publications
2018-02-01
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| Series: | Atmospheric Chemistry and Physics |
| Online Access: | https://www.atmos-chem-phys.net/18/2481/2018/acp-18-2481-2018.pdf |
| _version_ | 1819142376062451712 |
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| author | D. Zhao D. Zhao X. Song X. Song T. Zhu Z. Zhang Y. Liu J. Shang |
| author_facet | D. Zhao D. Zhao X. Song X. Song T. Zhu Z. Zhang Y. Liu J. Shang |
| author_sort | D. Zhao |
| collection | DOAJ |
| description | Heterogeneous/multiphase oxidation of SO<sub>2</sub> by NO<sub>2</sub> on solid or
aqueous particles is thought to be a potentially important source of sulfate
in the atmosphere, for example, during heavily polluted episodes (haze), but
the reaction mechanism and rate are uncertain. In this study, in order to
assess the importance of the direct oxidation of SO<sub>2</sub> by NO<sub>2</sub> we
investigated the heterogeneous/multiphase reaction of SO<sub>2</sub> with NO<sub>2</sub>
on individual CaCO<sub>3</sub> particles in N<sub>2</sub> using Micro-Raman spectroscopy.
In the SO<sub>2</sub> ∕ NO<sub>2</sub> ∕ H<sub>2</sub>O ∕ N<sub>2</sub> gas mixture, the
CaCO<sub>3</sub> solid particle was first converted to the Ca(NO<sub>3</sub>)<sub>2</sub>
droplet by the reaction with NO<sub>2</sub> and the deliquescence of
Ca(NO<sub>3</sub>)<sub>2</sub>, and then NO<sub>2</sub> oxidized SO<sub>2</sub> in the
Ca(NO<sub>3</sub>)<sub>2</sub> droplet forming CaSO<sub>4</sub>, which appeared as
needle-shaped crystals. Sulfate was mainly formed after the complete
conversion of CaCO<sub>3</sub> to Ca(NO<sub>3</sub>)<sub>2</sub>, that is, during the
multiphase oxidation of SO<sub>2</sub> by NO<sub>2</sub>. The precipitation of CaSO<sub>4</sub>
from the droplet solution promoted sulfate formation. The reactive uptake
coefficient of SO<sub>2</sub> for sulfate formation is on the order of 10<sup>−8</sup>,
and RH enhanced the uptake coefficient. We estimate that the direct
multiphase oxidation of SO<sub>2</sub> by NO<sub>2</sub> is not an important source of
sulfate in the ambient atmosphere compared with the SO<sub>2</sub> oxidation by OH
in the gas phase and is not as important as other aqueous-phase pathways,
such as the reactions of SO<sub>2</sub> with H<sub>2</sub>O<sub>2</sub>, O<sub>3</sub>, and O<sub>2</sub>,
with or without transition metals. |
| first_indexed | 2024-12-22T12:09:21Z |
| format | Article |
| id | doaj.art-6aba8bceb7ba4049a63769dd9eb57f3a |
| institution | Directory Open Access Journal |
| issn | 1680-7316 1680-7324 |
| language | English |
| last_indexed | 2024-12-22T12:09:21Z |
| publishDate | 2018-02-01 |
| publisher | Copernicus Publications |
| record_format | Article |
| series | Atmospheric Chemistry and Physics |
| spelling | doaj.art-6aba8bceb7ba4049a63769dd9eb57f3a2022-12-21T18:26:19ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242018-02-01182481249310.5194/acp-18-2481-2018Multiphase oxidation of SO<sub>2</sub> by NO<sub>2</sub> on CaCO<sub>3</sub> particlesD. Zhao0D. Zhao1X. Song2X. Song3T. Zhu4Z. Zhang5Y. Liu6J. Shang7BIC-ESAT and SKL-ESPC, College of Environmental Sciences and Engineering, Peking University, Beijing, 100871, ChinaThese authors contributed equally to this work.BIC-ESAT and SKL-ESPC, College of Environmental Sciences and Engineering, Peking University, Beijing, 100871, ChinaThese authors contributed equally to this work.BIC-ESAT and SKL-ESPC, College of Environmental Sciences and Engineering, Peking University, Beijing, 100871, ChinaBIC-ESAT and SKL-ESPC, College of Environmental Sciences and Engineering, Peking University, Beijing, 100871, ChinaBIC-ESAT and SKL-ESPC, College of Environmental Sciences and Engineering, Peking University, Beijing, 100871, ChinaBIC-ESAT and SKL-ESPC, College of Environmental Sciences and Engineering, Peking University, Beijing, 100871, ChinaHeterogeneous/multiphase oxidation of SO<sub>2</sub> by NO<sub>2</sub> on solid or aqueous particles is thought to be a potentially important source of sulfate in the atmosphere, for example, during heavily polluted episodes (haze), but the reaction mechanism and rate are uncertain. In this study, in order to assess the importance of the direct oxidation of SO<sub>2</sub> by NO<sub>2</sub> we investigated the heterogeneous/multiphase reaction of SO<sub>2</sub> with NO<sub>2</sub> on individual CaCO<sub>3</sub> particles in N<sub>2</sub> using Micro-Raman spectroscopy. In the SO<sub>2</sub> ∕ NO<sub>2</sub> ∕ H<sub>2</sub>O ∕ N<sub>2</sub> gas mixture, the CaCO<sub>3</sub> solid particle was first converted to the Ca(NO<sub>3</sub>)<sub>2</sub> droplet by the reaction with NO<sub>2</sub> and the deliquescence of Ca(NO<sub>3</sub>)<sub>2</sub>, and then NO<sub>2</sub> oxidized SO<sub>2</sub> in the Ca(NO<sub>3</sub>)<sub>2</sub> droplet forming CaSO<sub>4</sub>, which appeared as needle-shaped crystals. Sulfate was mainly formed after the complete conversion of CaCO<sub>3</sub> to Ca(NO<sub>3</sub>)<sub>2</sub>, that is, during the multiphase oxidation of SO<sub>2</sub> by NO<sub>2</sub>. The precipitation of CaSO<sub>4</sub> from the droplet solution promoted sulfate formation. The reactive uptake coefficient of SO<sub>2</sub> for sulfate formation is on the order of 10<sup>−8</sup>, and RH enhanced the uptake coefficient. We estimate that the direct multiphase oxidation of SO<sub>2</sub> by NO<sub>2</sub> is not an important source of sulfate in the ambient atmosphere compared with the SO<sub>2</sub> oxidation by OH in the gas phase and is not as important as other aqueous-phase pathways, such as the reactions of SO<sub>2</sub> with H<sub>2</sub>O<sub>2</sub>, O<sub>3</sub>, and O<sub>2</sub>, with or without transition metals.https://www.atmos-chem-phys.net/18/2481/2018/acp-18-2481-2018.pdf |
| spellingShingle | D. Zhao D. Zhao X. Song X. Song T. Zhu Z. Zhang Y. Liu J. Shang Multiphase oxidation of SO<sub>2</sub> by NO<sub>2</sub> on CaCO<sub>3</sub> particles Atmospheric Chemistry and Physics |
| title | Multiphase oxidation of SO<sub>2</sub> by NO<sub>2</sub> on CaCO<sub>3</sub> particles |
| title_full | Multiphase oxidation of SO<sub>2</sub> by NO<sub>2</sub> on CaCO<sub>3</sub> particles |
| title_fullStr | Multiphase oxidation of SO<sub>2</sub> by NO<sub>2</sub> on CaCO<sub>3</sub> particles |
| title_full_unstemmed | Multiphase oxidation of SO<sub>2</sub> by NO<sub>2</sub> on CaCO<sub>3</sub> particles |
| title_short | Multiphase oxidation of SO<sub>2</sub> by NO<sub>2</sub> on CaCO<sub>3</sub> particles |
| title_sort | multiphase oxidation of so sub 2 sub by no sub 2 sub on caco sub 3 sub particles |
| url | https://www.atmos-chem-phys.net/18/2481/2018/acp-18-2481-2018.pdf |
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