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@ARTICLE{Xiao:4682,
author = {Xiao, R. and Takegawa, N. and Kondo, Y. and Miyazaki, Y.
and Miyakawa, T. and Hu, M. and Shao, M. and Zeng, L.M. and
Hofzumahaus, A. and Holland, F. and Lu, K. and Sugimoto, N.
and Zhao, Y. and Zhang, Y.H.},
title = {{F}ormation of submicron sulfate and organic aerosols in
the outflow from the urban region of the {P}earl {R}iver
{D}elta in {C}hina},
journal = {Atmospheric environment},
volume = {43},
issn = {1352-2310},
address = {Amsterdam [u.a.]},
publisher = {Elsevier Science},
reportid = {PreJuSER-4682},
pages = {3754 - 3763},
year = {2009},
note = {This research was supported by China National Basic
Research and Development Programs 2002CB410801 and
2002CB211605. This work also was supported by the Ministry
of Education, Culture, Sports, Science, and Technology
(MEXT) and the global environment research fund of the
Japanese Ministry of the Environment (B-083). We thank the
China Scholarship Council for the scholarship supporting R.
Xiao at the University of Tokyo, Japan. The authors thank D.
Kodama, M. Shiraiwa. S. Han, P. Lin, and Z. Deng for their
support of the field experiments and Dr. X.D. Liu at the
Chinese Research Academy of Environmental Sciences and Dr.
Y.F. Cheng at the Leibniz-lnstitute for Tropospheric
Research for their constructive suggestions. We also would
like to thank the anonymous reviewers for their helpful
comments.},
abstract = {Size-resolved chemical compositions of non-refractory
submicron aerosols were measured using a quadrupole Aerodyne
aerosol mass spectrometer at a rural site near Guangzhou in
the Pearl River Delta (PRD) of China in the summer of 2006.
Two cases characterized as the outflows from the PRD urban
region with plumes of high SO2 concentration were
investigated. The evolution of sulfate size distributions
was observed on a timescale of several hours. Namely mass
concentrations of sulfate in the condensation mode (with
vacuum aerodynamic diameters (D-va) < 300 nm) increased at a
rate of about 0.17-0.37 ppbv h(-1) during the daytime. This
finding was consistent with the sulfuric acid production
rates of about 0.17-0.3 ppbv h(-1), as calculated from the
observed gas-phase concentrations of OH (similar to 3.3 x
10(6)-1.7 x 10(7) cm(-3)) and SO2 (similar to 3-21.2 ppbv).
This implies that the growth of sulfate in the condensation
mode was mainly due to gas-phase oxidation of SO2. The
observed rapid increase was caused mainly by the concurrent
high concentrations of OH and SO2 in the air mass. The
evolution of the mass size distributions of m/z 44, a tracer
for oxygenated organic aerosol (OOA), was very similar to
that of sulfate. The mass loadings of m/z 44 were strongly
correlated with those of sulfate (r(2) = 0.99) in the
condensation mode, indicating that ODA might also be formed
by the gas-phase oxidation of volatile organic compound
(VOC) precursors. It is likely that sulfate and ODA were
internally mixed throughout the whole size range in the air
mass. (C) 2009 Elsevier Ltd. All rights reserved.},
keywords = {J (WoSType)},
cin = {ICG-2},
ddc = {550},
cid = {I:(DE-Juel1)VDB791},
pnm = {Atmosphäre und Klima},
pid = {G:(DE-Juel1)FUEK406},
shelfmark = {Environmental Sciences / Meteorology $\&$ Atmospheric
Sciences},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000268609000012},
doi = {10.1016/j.atmosenv.2009.04.028},
url = {https://juser.fz-juelich.de/record/4682},
}