<p>Carbonate radical anion (<InlineEquation ID="IEq1"> <InlineMediaObject> <ImageObject Color="BlackWhite" FileRef="41612_2025_905_Article_IEq1.gif" Format="GIF" Height="17" Rendition="HTML" Resolution="72" Type="Linedraw" Width="43" /> </InlineMediaObject> <EquationSource Format="TEX">\({{\rm{CO}}}_{{3}^{.-}}\)</EquationSource> <EquationSource Format="MATHML"><math> <msub> <mrow> <mi mathvariant="normal">CO</mi> </mrow> <mrow> <msup> <mrow> <mn>3</mn> </mrow> <mrow> <mo>.</mo> <mo>−</mo> </mrow> </msup> </mrow> </msub> </math></EquationSource> </InlineEquation>) is generally considered as a marginal intermediate that rarely regulates atmospheric-relevant reactions of significance. Unexpectedly, in this work, employing a suit of the in-field measurements, lab-based validations, improved kinetic numerical calculations, and chemical transport modeling, we demonstrate that <InlineEquation ID="IEq2"> <InlineMediaObject> <ImageObject Color="BlackWhite" FileRef="41612_2025_905_Article_IEq2.gif" Format="GIF" Height="17" Rendition="HTML" Resolution="72" Type="Linedraw" Width="43" /> </InlineMediaObject> <EquationSource Format="TEX">\({{\rm{CO}}}_{{3}^{.-}}\)</EquationSource> <EquationSource Format="MATHML"><math> <msub> <mrow> <mi mathvariant="normal">CO</mi> </mrow> <mrow> <msup> <mrow> <mn>3</mn> </mrow> <mrow> <mo>.</mo> <mo>−</mo> </mrow> </msup> </mrow> </msub> </math></EquationSource> </InlineEquation> gives a significantly overlooked contribution (~54.4%) to overall secondary sulfate formation during dust storm-relevant episodes and ~236.3% increase of SO<sub>2</sub> uptake over mineral dust pathway during haze-relevant periods. GEOS-Chem modeling results further emphasize the important position of this radical ion in dust-driven SO<sub>2</sub> oxidation chemistry. Our finding leaves this active intermediate no longer a marginal oxidant currently prevailing in the framework of the atmospheric science community. More importantly, after considering this rapid dust-driven sulfate formation channel mediated by carbonate radicals during pollution episodes, this study provides a clear indication that high priority should be given to reducing alkaline soil dust emissions to achieve benefits for air quality.</p>

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Carbonate radical ion as a key driver of rapid atmospheric sulfate formation

  • Yangyang Liu,
  • Xiao Li,
  • Qiuyue Ge,
  • Xiaozhong Fang,
  • Tao Wang,
  • Wenbo You,
  • Wei Wang,
  • Lifang Xie,
  • Kejian Li,
  • Kedong Gong,
  • Le Yang,
  • Runbo Wang,
  • Jilun Wang,
  • Licheng Wang,
  • Minglu Ma,
  • Tingting Huang,
  • Hongbo Fu,
  • Jianmin Chen,
  • Xinyi Dong,
  • Liwu Zhang

摘要

Carbonate radical anion ( \({{\rm{CO}}}_{{3}^{.-}}\) CO 3 . ) is generally considered as a marginal intermediate that rarely regulates atmospheric-relevant reactions of significance. Unexpectedly, in this work, employing a suit of the in-field measurements, lab-based validations, improved kinetic numerical calculations, and chemical transport modeling, we demonstrate that \({{\rm{CO}}}_{{3}^{.-}}\) CO 3 . gives a significantly overlooked contribution (~54.4%) to overall secondary sulfate formation during dust storm-relevant episodes and ~236.3% increase of SO2 uptake over mineral dust pathway during haze-relevant periods. GEOS-Chem modeling results further emphasize the important position of this radical ion in dust-driven SO2 oxidation chemistry. Our finding leaves this active intermediate no longer a marginal oxidant currently prevailing in the framework of the atmospheric science community. More importantly, after considering this rapid dust-driven sulfate formation channel mediated by carbonate radicals during pollution episodes, this study provides a clear indication that high priority should be given to reducing alkaline soil dust emissions to achieve benefits for air quality.