Molecular characterization of atmospheric particulate organosulfates in three megacities at the middle and lower reaches of the Yangtze River
PM<sub>2.5</sub> filter samples have been collected in three megacities at the middle and lower reaches of the Yangtze River: Wuhan (WH), Nanjing (NJ), and Shanghai (SH). The samples were analyzed using ultra-high-performance liquid chromatography (UHPLC) coupled with Orbitrap mass s...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Copernicus Publications
2016-02-01
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Series: | Atmospheric Chemistry and Physics |
Online Access: | https://www.atmos-chem-phys.net/16/2285/2016/acp-16-2285-2016.pdf |
Summary: | PM<sub>2.5</sub> filter samples have been collected in three megacities
at the middle and lower reaches of the Yangtze River: Wuhan (WH), Nanjing
(NJ), and Shanghai (SH). The samples were analyzed using
ultra-high-performance liquid chromatography (UHPLC) coupled with Orbitrap
mass spectrometry (MS), which allowed for detection of about 200 formulas of
particulate organosulfates (OSs), including dozens of formulas of
nitrooxy-organosulfates, with various numbers of isomers for each
tentatively determined formula at each location. The number of aliphatic OS
formulas represented more than 78 % of the detected OSs at the three
locations, while aromatic OSs were much less numerous. OSs with two to four
isomers accounted for about 50 % of the total OSs on average in these
megacity samples, and the percentage of OSs with six and more isomers in the
WH sample was more significant than those in the SH and NJ samples.
Additionally, the molecular formula, average molecular weight, and degrees
of oxidation and unsaturation of tentatively assigned OSs were compared. The
results indicate that the OSs between NJ and SH shared higher similarity,
and the characteristics of OSs in SH varied diurnally and seasonally. OSs
derived from isoprene, monoterpenes, and sesquiterpenes were abundant in
samples from the three megacities and could be produced through both daytime
photochemistry and NO<sub>3</sub> night-time chemistry. The reaction pathways
leading to isoprene-derived OSs probably varied in those locations because
of the different NO<sub><i>x</i></sub> levels. In addition, a number of OSs that might be
formed from polycyclic aromatic hydrocarbons were also detected, which
underlies the importance of anthropogenic sources for this class of
compounds. |
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ISSN: | 1680-7316 1680-7324 |