4.7 Article

Molecular characteristics, sources, and formation pathways of organosulfur compounds in ambient aerosol in Guangzhou, South China

期刊

ATMOSPHERIC CHEMISTRY AND PHYSICS
卷 22, 期 10, 页码 6919-6935

出版社

COPERNICUS GESELLSCHAFT MBH
DOI: 10.5194/acp-22-6919-2022

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资金

  1. National Key R&D Program of China [2018YFC1802801]
  2. National Natural Science Foundation of China [42192514, 41977177]
  3. Guangdong Foundation for Program of Science and Technology Research [2019B121205006, 2020B1212060053]
  4. Guangzhou Foundation for Program of Science and Technology Research [202102080251]

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This study reported the abundance and molecular composition of organic sulfur compounds (OrgSs) in fine particulate samples collected in Guangzhou. The results revealed positive correlations of organic sulfur with sulfur dioxide and oxidants. Fourier transform ion cyclotron resonance mass spectrometry analysis showed that most sulfur-containing formulas detected in the samples were oxidized organosulfates or nitrooxy organosulfates.
Organosulfur compounds (OrgSs), especially organosulfates, have been widely reported to be present in large quantities in particulate organic matter found in various atmospheric environments. Despite hundreds of organosulfates and their formation mechanisms being previously identified, a large fraction of OrgSs remain unexplained at the molecular level, and a better understanding of their formation pathways and critical environmental parameters is required to explain the variations in their concentrations. In this study, the abundance and molecular composition of OrgSs in fine particulate samples collected in Guangzhou were reported. The results revealed that the ratio of the annual average mass of organic sulfur to total particulate sulfur was 33 +/- 12 %, and organic sulfur had positive correlations with SO2 (r = 0.37, p < 0.05) and oxidant (NOx + O-3, r = 0.40, p < 0.01). A Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) analysis revealed that more than 80 % of the sulfur-containing formulas detected in the samples had the elemental composition of o/(4s + 3n) >= 1, indicating that they were largely in the form of oxidized organosulfates or nitrooxy organosulfates. Many OrgSs that were previously tentatively identified as having biogenic or anthropogenic origins were also present in freshly emitted aerosols derived from combustion sources. The results indicated that the formation of OrgSs through an epoxide intermediate pathway could account for up to 46 % of OrgSs from an upper bound estimation, and the oxidant levels could explain 20 % of the variation in the mass of organic sulfur. The analysis of our large dataset of FT-ICR MS results suggested that relative humidity, oxidation of biogenic volatile organic compounds via ozonolysis, and NOx-related nitrooxy organosulfate formation were the major reasons for the molecular variation of OrgSs, possibly highlighting the importance of the acid-catalyzed ring-opening of epoxides, oxidation processes, and heterogeneous reactions involving either the uptake of SO2 or the heterogeneous oxidation of particulate organosulfates into additional unrecognized OrgSs.

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