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Ion-molecule interactions enable unexpected phase transitions in organic-inorganic aerosol.


ABSTRACT: Atmospheric aerosol particles are commonly complex, aqueous organic-inorganic mixtures, and accurately predicting the properties of these particles is essential for air quality and climate projections. The prevailing assumption is that aqueous organic-inorganic aerosols exist predominately with liquid properties and that the hygroscopic inorganic fraction lowers aerosol viscosity relative to the organic fraction alone. Here, in contrast to those assumptions, we demonstrate that increasing inorganic fraction can increase aerosol viscosity (relative to predictions) and enable a humidity-dependent gel phase transition through cooperative ion-molecule interactions that give rise to long-range networks of atmospherically relevant low-mass oxygenated organic molecules (180 to 310 Da) and divalent inorganic ions. This supramolecular, ion-molecule effect can drastically influence the phase and physical properties of organic-inorganic aerosol and suggests that aerosol may be (semi)solid under more conditions than currently predicted. These observations, thus, have implications for air quality and climate that are not fully represented in atmospheric models.

SUBMITTER: Richards DS 

PROVIDER: S-EPMC7673807 | biostudies-literature | 2020 Nov

REPOSITORIES: biostudies-literature

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Ion-molecule interactions enable unexpected phase transitions in organic-inorganic aerosol.

Richards David S DS   Trobaugh Kristin L KL   Hajek-Herrera Josefina J   Price Chelsea L CL   Sheldon Craig S CS   Davies James F JF   Davis Ryan D RD  

Science advances 20201118 47


Atmospheric aerosol particles are commonly complex, aqueous organic-inorganic mixtures, and accurately predicting the properties of these particles is essential for air quality and climate projections. The prevailing assumption is that aqueous organic-inorganic aerosols exist predominately with liquid properties and that the hygroscopic inorganic fraction lowers aerosol viscosity relative to the organic fraction alone. Here, in contrast to those assumptions, we demonstrate that increasing inorga  ...[more]

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