% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Zhao:155322,
author = {Zhao, Defeng and Kaminski, M. and Schlag, P. and Fuchs, H.
and Acir, I.-H. and Bohn, B. and Häseler, R. and
Kiendler-Scharr, A. and Rohrer, F. and Tillmann, R. and
Wang, Mingjin and Wegener, R. and Wildt, J. and Wahner, A.
and Mentel, T. F.},
title = {{S}econdary {O}rganic {A}erosol ({SOA}) formation from
hydroxyl radical oxidation and ozonolysis of monoterpenes},
journal = {Atmospheric chemistry and physics / Discussions},
volume = {14},
number = {9},
issn = {1680-7375},
address = {Katlenburg-Lindau},
publisher = {EGU},
reportid = {FZJ-2014-04495},
pages = {12591 - 12634},
year = {2014},
abstract = {Oxidation by hydroxyl radical (OH) and ozonolysis are the
two major pathways of daytime biogenic volatile organic
compounds (VOCs) oxidation and secondary organic aerosol
(SOA) formation. In this study, we investigated the particle
formation of several common monoterpenes (α-pinene,
β-pinene, and limonene) by OH dominated oxidation, which
has seldom been investigated. OH oxidation experiments were
carried out in the SAPHIR chamber in Jülich, Germany, at
low NOx (0.01–1 ppbV) and low ozone (O3) concentration. OH
concentration and OH reactivity were measured directly so
that the overall reaction rates of organic compounds with OH
were quantified. Multi-generation reaction process, particle
growth, new particle formation, particle yield, and chemical
composition were analyzed and compared with that of
monoterpene ozonolysis. Multi-generation products were found
to be important in OH dominated SOA formation. The relative
role of functionalization and fragmentation in the reaction
process of OH oxidation was analyzed by examining the
particle mass and the particle size as a function of OH
dose. We developed a novel method which quantitatively links
particle growth to the reaction of OH with organics in a
reaction system. This method was also used to analyze the
evolution of functionalization and fragmentation of organics
in the particle formation by OH oxidation. It shows that
functionalization of organics was dominant in the beginning
of the reaction (within two lifetimes of the monoterpene)
and fragmentation started to be dominant after that. We
compared particle formation from OH oxidation with that from
pure ozonolysis. In individual experiments, growth rates of
the particle size did not necessarily correlate with the
reaction rate of monoterpene with OH and O3. Comparing the
size growth rates at the similar reaction rates of
monoterpene with OH or O3 indicates that generally, OH
oxidation and ozonolysis had similar efficiency in particle
growth. The SOA yield of α-pinene and limonene by
ozonolysis was higher than that of OH oxidation. Aerosol
mass spectrometry (AMS) shows SOA elemental composition from
OH oxidation follows a slope shallower than −1 in the O /
C vs. H / C diagram, indicating that oxidation proceeds
without significant loss of hydrogen. SOA from OH oxidation
had higher H / C ratios than SOA from ozonolysis. In
ozonolysis, a process with significant hydrogen loss seemed
to play an important role in SOA formation.},
cin = {IEK-8 / IBG-2},
ddc = {550},
cid = {I:(DE-Juel1)IEK-8-20101013 / I:(DE-Juel1)IBG-2-20101118},
pnm = {233 - Trace gas and aerosol processes in the troposphere
(POF2-233) / HITEC - Helmholtz Interdisciplinary Doctoral
Training in Energy and Climate Research (HITEC)
(HITEC-20170406)},
pid = {G:(DE-HGF)POF2-233 / G:(DE-Juel1)HITEC-20170406},
typ = {PUB:(DE-HGF)16},
doi = {10.5194/acpd-14-12591-2014},
url = {https://juser.fz-juelich.de/record/155322},
}