Issue 11, 2024

Impact of atmospheric water-soluble iron on α-pinene-derived SOA formation and transformation in the presence of aqueous droplets

Abstract

The impact of water-soluble atmospheric iron on formation, growth and aging of secondary organic aerosol (SOA) is a controversial subject in the literature. Iron chemistry drives Fenton reactions in the aqueous phase which is dependent on pH. Flow reactor experiments in the dark and under humid conditions were conducted to investigate systematically the influence of ferrous iron in the aqueous phase on α-pinene SOA by online physical analysis and offline high-resolution mass spectrometry. During the experiments increased SOA formation under conditions favorable for dark Fenton chemistry in the aqueous phase was observed. Furthermore, samples with an acidified and iron-containing aqueous phase showed a degradation of pinyl-diaterpenyl (C17H26O8) ester which ages through oxidation via OH radicals and can thus be evidence for ongoing degradation processes of high molecular weight molecules by iron chemistry. Moreover, higher abundance of dimer MW338 (C19H30O5) in the acidic sample affected by Fenton's chemistry was detected which is suggested to be formed via acid catalysis indicating competing acidity-driven reactions influencing SOA formation. Therefore, this study provides insight into the impact of aqueous phase iron on SOA formation and transformation under simulated natural conditions.

Graphical abstract: Impact of atmospheric water-soluble iron on α-pinene-derived SOA formation and transformation in the presence of aqueous droplets

Supplementary files

Article information

Article type
Paper
Submitted
02 Jul 2024
Accepted
12 Sep 2024
First published
14 Sep 2024
This article is Open Access
Creative Commons BY license

Environ. Sci.: Atmos., 2024,4, 1218-1228

Impact of atmospheric water-soluble iron on α-pinene-derived SOA formation and transformation in the presence of aqueous droplets

S. Lüchtrath, S. Klemer, C. Dubois, C. George and A. Held, Environ. Sci.: Atmos., 2024, 4, 1218 DOI: 10.1039/D4EA00095A

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