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  Aerosol pH and Ion Activities of HSO4- and SO42-in Supersaturated Single Droplets

Li, M., Su, H., Zheng, G., Kuhn, U., Kim, N., Li, G., et al. (2022). Aerosol pH and Ion Activities of HSO4- and SO42-in Supersaturated Single Droplets. Environmental Science & Technology, 56(18), 12863 -12872. doi:10.1021/acs.est.2c01378.

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 Creators:
Li, Meng1, Author           
Su, Hang1, Author           
Zheng, Guangjie1, Author           
Kuhn, Uwe1, Author           
Kim, Najin1, Author           
Li, Guo1, Author           
Ma, Nan1, Author           
Pöschl, Ulrich1, Author           
Cheng, Yafang1, Author           
Affiliations:
1Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society, ou_1826290              

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 Abstract: Accurate determination of acidity (pH) and ion activities in aqueous droplets is a major experimental and theoretical challenge for understanding and simulating atmospheric multiphase chemistry. Here, we develop a ratiometric Raman spectroscopy method to measure the equilibrium concentration of sulfate (SO42–) and bisulfate (HSO4–) in single microdroplets levitated by aerosol optical tweezers. This approach enables determination of ion activities and pH in aqueous sodium bisulfate droplets under highly supersaturated conditions. The experimental results were compared against aerosol thermodynamic model calculations in terms of simulating aerosol ion concentrations, ion activity coefficients, and pH. We found that the Extended Aerosol Inorganics Model (E-AIM) can well reproduce the experimental results. The alternative model ISORROPIA, however, exhibits substantial deviations in SO42– and HSO4– concentrations and up to a full unit of aerosol pH under acidic conditions, mainly due to discrepancies in simulating ion activity coefficients of SO42––HSO4– equilibrium. Globally, this may cause an average deviation of ISORROPIA from E-AIM by 25 and 65% in predicting SO42– and HSO4– concentrations, respectively. Our results show that it is important to determine aerosol pH and ion activities in the investigation of sulfate formation and related aqueous phase chemistry.

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Language(s): eng - English
 Dates: 2022-09-01
 Publication Status: Published online
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 Identifiers: DOI: 10.1021/acs.est.2c01378
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Title: Environmental Science & Technology
  Abbreviation : Environ. Sci. Technol.
Source Genre: Journal
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Publ. Info: Easton, PA : American Chemical Society
Pages: - Volume / Issue: 56 (18) Sequence Number: - Start / End Page: 12863 - 12872 Identifier: ISSN: 0013-936X
CoNE: https://pure.mpg.de/cone/journals/resource/954921342157