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Multiphase Buffering by Ammonia Sustains Sulfate Production in Atmospheric Aerosols

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Zheng,  Guangjie
Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Andreae,  Meinrat O.
Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Pöschl,  Ulrich
Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

/persons/resource/persons127588

Cheng,  Yafang
Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Citation

Zheng, G., Su, H., Andreae, M. O., Pöschl, U., & Cheng, Y. (2024). Multiphase Buffering by Ammonia Sustains Sulfate Production in Atmospheric Aerosols. AGU Advances, 5(4): e2024AV001238. doi:10.1029/2024AV001238.


Cite as: https://hdl.handle.net/21.11116/0000-000F-D82D-C
Abstract
Multiphase oxidation of sulfur dioxide (SO2) is an important source of sulfate in the atmosphere. There are, however, concerns that protons produced during SO2 oxidation may cause rapid acidification of aerosol water and thereby quickly shut down the fast reactions favored at high pH. Here, we show that the sustainability of sulfate production is controlled by the competing effects of multiphase buffering and acidification, which can be well described by a characteristic buffering time, τbuff. Both GEOS-Chem simulations and observations show that globally, τbuff is long enough (days) to sustain sulfate production over most populated regions, where the acidification of aerosol water is counteracted by the strong buffering effect of NH4+/NH3. Our results highlight the importance of anthropogenic ammonia emissions and pervasive human influences in shaping the chemical environment of the atmosphere.