Unveiling a large fraction of hidden organosulfates in ambient organic aerosol

Organosulfates are key compounds driving the anthropogenic enhancement of ambient organic aerosol, however, total organosulfate quantification remains elusive due to their molecular diversity and the scarcity of authentic standards. Here, we present a solid-phase extraction method that isolates organosulfates from ambient aerosol samples and enables their identification and quantification using mass spectrometry and a charged aerosol detector, respectively. We investigate ambient aerosol samples from urban China and rural Germany and quantify ~130 and ~65 chromatographically resolved organosulfates, respectively, contributing less than ~2% to the total organic matter. We find a significantly larger organosulfate fraction appearing as a broad peak in the chromatograms from the charged aerosol detector. Confirming its origin from chromatographically non-resolved organosulfates, an all-ion fragmentation experiment reveals specific sulfate-related ions. Integrating this peak, we find the contribution of organosulfates to organic aerosol is 12-17% and ~21% in samples from urban China and rural Germany, respectively. These findings emphasise the potential of sulfur emission reduction for mitigating both sulfate-related and organic aerosol pollution.

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Publication Details

Journal
Nature Communications
Published
2025-05-01
DOI
https://doi.org/10.1038/s41467-025-59420-y
Citations
6
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
7.80

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article

Unveiling a large fraction of hidden organosulfates in ambient organic aerosol

Alexander L. Vogel, Bangjun Liu, Stefanie Hildmann, Julia David et al.
6 citations
Nature Communications
Atmospheric chemistry and aerosols
7.80
article

Unveiling a large fraction of hidden organosulfates in ambient organic aerosol

Alexander L. Vogel, Bangjun Liu, Stefanie Hildmann, Julia David, Julian Rüdiger, Thorsten Hoffmann, Natalie Reininger, Jialiang Ma, Zhijun Wu, Yanting Qiu, Florian Ungeheuer, Yingbin Xue, Mario Simon, Anna Breuninger, Cunliang Zhao, Lili Li, Hongya Niu, Yushan Li, L D’Angelo, Yuchen Wang, Y. Bai, Damian Döbler
article en
6 citations

Abstract

Organosulfates are key compounds driving the anthropogenic enhancement of ambient organic aerosol, however, total organosulfate quantification remains elusive due to their molecular diversity and the scarcity of authentic standards. Here, we present a solid-phase extraction method that isolates organosulfates from ambient aerosol samples and enables their identification and quantification using mass spectrometry and a charged aerosol detector, respectively. We investigate ambient aerosol samples from urban China and rural Germany and quantify ~130 and ~65 chromatographically resolved organosulfates, respectively, contributing less than ~2% to the total organic matter. We find a significantly larger organosulfate fraction appearing as a broad peak in the chromatograms from the charged aerosol detector. Confirming its origin from chromatographically non-resolved organosulfates, an all-ion fragmentation experiment reveals specific sulfate-related ions. Integrating this peak, we find the contribution of organosulfates to organic aerosol is 12-17% and ~21% in samples from urban China and rural Germany, respectively. These findings emphasise the potential of sulfur emission reduction for mitigating both sulfate-related and organic aerosol pollution.

Nature CommunicationsVol. 16(1)
Hebei University of Engineering (CN), Goethe University Frankfurt (DE), Hunan University (CN), Johannes Gutenberg University Mainz (DE), Peking University (CN), Frankfurt Institute for Advanced Studies (DE), State Key Joint Laboratory of Environment Simulation and Pollution Control (CN), German Environment Agency (DE)
Deutsche Forschungsgemeinschaft, National Natural Science Foundation of China, China Scholarship Council, State Key Laboratory of Loess and Quaternary Geology
Openalex Percentile: Top 2%
Atmospheric chemistry and aerosols
7.80
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