Relative humidity and O 3 concentration as two prerequisites for sulfate formation
Sulfate formation mechanisms have been discussed extensively but are still disputed. In this work, a year-long particulate matter (PM2.5) sampling campaign was conducted together with measurements of gaseous pollutant concentrations and meteorological parameters in Beijing, China, from March 2012 to...
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Published in | Atmospheric chemistry and physics Vol. 19; no. 19; pp. 12295 - 12307 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
02.10.2019
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Online Access | Get full text |
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Summary: | Sulfate formation mechanisms have been discussed
extensively but are still disputed. In this work, a year-long particulate
matter (PM2.5) sampling campaign was conducted together with
measurements of gaseous pollutant concentrations and meteorological
parameters in Beijing, China, from March 2012 to February 2013. The sulfur
oxidation ratio (SOR), an indicator of secondary sulfate formation,
displayed a clear summer peak and winter valley, even though no obvious
seasonal variations in sulfate mass concentration were observed. A rapid
rise in the SOR was found at a relative humidity (RH) threshold of ∼45 % or an
O3 concentration threshold of ∼35 ppb, allowing us to
first introduce the idea that RH and O3 concentrations are two
prerequisites for rapid sulfate formation via multiphase reactions. In the
case of the RH threshold, this is consistent with current understanding of
the multiphase formation of sulfate, since it relates to the
semisolid-to-liquid phase transition of atmospheric aerosols. Correlation
analysis between SOR and aerosol water content (AWC) further backed this up. In the case of the
O3 concentration threshold, this is consistent with the consumption of
liquid oxidants in multiphase sulfate formation. The thresholds introduced
here lead us to a better understanding of the sulfate formation mechanisms and
sulfate formation variations. H2O2 might be the major oxidant of
sulfate formation, since another liquid-phase oxidant, O3, has
previously been shown to be unimportant. The seasonal variations in sulfate
formation could be accounted for by variations in the RH and O3
prerequisites. For example, over the year-long study, the fastest
SO2-to-sulfate conversion occurred in summer, which was associated with
the highest values of O3 (and also H2O2) concentration and
RH. The SOR also displayed variations with pollution levels; i.e. the SOR
increased with PM2.5 in all seasons. Such variations were primarily
associated with a transition from the slow gas-phase formation of sulfate to
rapid multiphase reactions, since RH increased higher than its prerequisite
value of around 45 % as pollution evolved. In addition, the self-catalytic
nature of sulfate formation (i.e. the formation of hydrophilic sulfate
aerosols under high RH conditions results in an increase in aerosol water
content, which results in greater particle volume for further multiphase
sulfate formation) also contributed to variations among the pollution
scenarios. |
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ISSN: | 1680-7324 1680-7324 |
DOI: | 10.5194/acp-19-12295-2019 |