4.8 Article

Response of the Aerodyne Aerosol Mass Spectrometer to Inorganic Sulfates and Organosulfur Compounds: Applications in Field and Laboratory Measurements

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 53, Issue 9, Pages 5176-5186

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.9b00884

Keywords

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Funding

  1. NSF [AGS-1822664, AGS-1242258, AGS-1455588]
  2. U.S. Environmental Protection Agency STAR grant [RD-83540301]
  3. EPA STAR grant [83540101]
  4. EPA [RD-83540301]
  5. Horizon 2020 research and innovation programme ACTRIS-2 Integrating Activities [654109]
  6. EPA-Ireland (AEROSOURCE) [2016-CCRP-MS-31]
  7. Polarstern expedition [AWI_ANT XXVII/4]
  8. Gottfried Wilhelm Leibniz Association (OCEANET project)
  9. NASA [NNX15AT96G]
  10. Environmental Protection Agency Ireland (EPA) [2016-CCRP-MS.31] Funding Source: Environmental Protection Agency Ireland (EPA)

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Organosulfur compounds are important components of secondary organic aerosols (SOA). While the Aerodyne high-resolution time-of-flight aerosol mass spectrometer (AMS) has been extensively used in aerosol studies, the response of the AMS to organosulfur compounds is not well-understood. Here, we investigated the fragmentation patterns of organosulfurs and inorganic sulfates in the AMS, developed a method to deconvolve total sulfate into components of inorganic and organic origins, and applied this method in both laboratory and field measurements. Apportionment results from laboratory isoprene photooxidation experiment showed that with inorganic sulfate seed, sulfate functionality of organic origins can contribute similar to 7% of SOA mass at peak growth. Results from measurements in the Southeastern U.S. showed that 4% of measured sulfate is from organosulfur compounds. Methanesulfonic acid was estimated for measurements in the coastal and remote marine boundary layer. We explored the application of this method to unit mass-resolution data, where it performed less well due to interferences. Our apportionment results demonstrate that organosulfur compounds could be a non-negligible source of sulfate fragments in AMS laboratory and field data sets. A reevaluation of previous AMS measurements over the full range of atmospheric conditions using this method could provide a global estimate/constraint on the contribution of organosulfur compounds.

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