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@ARTICLE{vonHobe:1015297,
author = {von Hobe, Marc and Taraborrelli, Domenico and Alber, Sascha
and Bohn, Birger and Dorn, Hans-Peter and Fuchs, Hendrik and
Li, Yun and Qiu, Chenxi and Rohrer, Franz and Sommariva,
Roberto and Stroh, Fred and Tan, Zhaofeng and Wedel, Sergej
and Novelli, Anna},
title = {{M}easurement report: {C}arbonyl sulfide production during
dimethyl sulfide oxidation in the atmospheric simulation
chamber {SAPHIR}},
journal = {Atmospheric chemistry and physics},
volume = {23},
number = {18},
issn = {1680-7316},
address = {Katlenburg-Lindau},
publisher = {EGU},
reportid = {FZJ-2023-03642},
pages = {10609 - 10623},
year = {2023},
abstract = {Carbonyl sulfide (OCS), the most abundant sulfur gas in the
Earth's atmosphere, is a greenhouse gas, a precursor to
stratospheric sulfate aerosol, and a proxy for terrestrial
CO2 uptake. Estimates of important OCS sources and sinks
still have significant uncertainties and the global budget
is not considered closed. One particularly uncertain source
term, the OCS production during the atmospheric oxidation of
dimethyl sulfide (DMS) emitted by the oceans, is addressed
by a series of experiments in the atmospheric simulation
chamber SAPHIR in conditions comparable to the remote marine
atmosphere. DMS oxidation was initiated with OH and/or Cl
radicals and DMS, OCS, and several oxidation products and
intermediates were measured, including hydroperoxymethyl
thioformate (HPMTF), which was recently found to play a key
role in DMS oxidation in the marine atmosphere. One
important finding is that the onset of HPMTF and OCS
formation occurred faster than expected from the current
chemical mechanisms. In agreement with other recent studies,
OCS yields between $9 \%$ and $12 \%$ were observed in
our experiments. Such yields are substantially higher than
the $0.7 \%$ yield measured in laboratory experiments in
the 1990s, which is generally used to estimate the indirect
OCS source from DMS in global budget estimates. However, we
do not expect the higher yields found in our experiments to
directly translate into a substantially higher OCS source
from DMS oxidation in the real atmosphere, where conditions
are highly variable, and, as pointed out in recent work,
heterogeneous HPMTF loss is expected to effectively limit
OCS production via this pathway. Together with other
experimental studies, our results will be helpful to further
elucidate the DMS oxidation chemical mechanism and in
particular the paths leading to OCS formation.},
cin = {IEK-7 / IEK-8},
ddc = {550},
cid = {I:(DE-Juel1)IEK-7-20101013 / I:(DE-Juel1)IEK-8-20101013},
pnm = {2111 - Air Quality (POF4-211) / 2112 - Climate Feedbacks
(POF4-211)},
pid = {G:(DE-HGF)POF4-2111 / G:(DE-HGF)POF4-2112},
typ = {PUB:(DE-HGF)16},
UT = {WOS:001161773700001},
doi = {10.5194/acp-23-10609-2023},
url = {https://juser.fz-juelich.de/record/1015297},
}