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@ARTICLE{Sarrafzadeh:818333,
author = {Sarrafzadeh, Mehrnaz and Wildt, Jürgen and Pullinen, Iida
and Springer, Monika and Kleist, Einhard and Tillmann, Ralf
and Schmitt, Sebastian and Wu, Cheng and Mentel, Thomas F.
and Zhao, Defeng and Hastie, Donald R. and Kiendler-Scharr,
Astrid},
title = {{I}mpact of {NO}x and {OH} on secondary organic aerosol
formation from β-pinene photooxidation},
journal = {Atmospheric chemistry and physics},
volume = {16},
number = {17},
issn = {1680-7324},
address = {Katlenburg-Lindau},
publisher = {EGU},
reportid = {FZJ-2016-04805},
pages = {11237 - 11248},
year = {2016},
abstract = {In this study, the NOx dependence of secondary organic
aerosol (SOA) formation from photooxidation of the biogenic
volatile organic compound (BVOC) β-pinene was
comprehensively investigated in the Jülich Plant Atmosphere
Chamber. Consistent with the results of previous NOx studies
we found increases of SOA yields with increasing [NOx] at
low-NOx conditions ([NOx]0 < 30 ppb,
[BVOC]0 ∕ [NOx]0 > 10 ppbC ppb−1).
Furthermore, increasing [NOx] at high-NOx conditions
([NOx]0 > 30 ppb,
[BVOC]0 ∕ [NOx]0 ∼ 10 to
∼ 2.6 ppbC ppb−1) suppressed the SOA yield.
The increase of SOA yield at low-NOx conditions was
attributed to an increase of OH concentration, most probably
by OH recycling in NO + HO2 → NO2 + OH
reaction. Separate measurements without NOx addition but
with different OH primary production rates confirmed the OH
dependence of SOA yields. After removing the effect of OH
concentration on SOA mass growth by keeping the OH
concentration constant, SOA yields only decreased with
increasing [NOx]. Measuring the NOx dependence of SOA yields
at lower [NO] ∕ [NO2] ratio showed less pronounced
increase in both OH concentration and SOA yield. This result
was consistent with our assumption of OH recycling by NO and
to SOA yields being dependent on OH concentrations. Our
results furthermore indicated that NOx dependencies vary for
different NOx compositions. A substantial fraction of the
NOx-induced decrease of SOA yields at high-NOx conditions
was caused by NOx-induced suppression of new particle
formation (NPF), which subsequently limits the particle
surface where low volatiles condense. This was shown by
probing the NOx dependence of SOA formation in the presence
of seed particles. After eliminating the effect of
NOx-induced suppression of NPF and NOx-induced changes of OH
concentrations, the remaining effect of NOx on the SOA yield
from β-pinene photooxidation was moderate. Compared to
β-pinene, the SOA formation from α-pinene photooxidation
was only suppressed by increasing NOx. However, basic
mechanisms of the NOx impacts were the same as that of
β-pinene.},
cin = {IEK-8 / IBG-2},
ddc = {550},
cid = {I:(DE-Juel1)IEK-8-20101013 / I:(DE-Juel1)IBG-2-20101118},
pnm = {243 - Tropospheric trace substances and their
transformation processes (POF3-243) / HITEC - Helmholtz
Interdisciplinary Doctoral Training in Energy and Climate
Research (HITEC) (HITEC-20170406)},
pid = {G:(DE-HGF)POF3-243 / G:(DE-Juel1)HITEC-20170406},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000384199500002},
doi = {10.5194/acp-16-11237-2016},
url = {https://juser.fz-juelich.de/record/818333},
}