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@ARTICLE{Gkatzelis:838710,
author = {Gkatzelis, Georgios and Tillmann, Ralf and Hohaus, Thorsten
and Müller, Markus and Eichler, Philipp and Xu, Kang-Ming
and Schlag, Patrick and Schmitt, Sebastian H. and Wegener,
Robert and Kaminski, Martin and Holzinger, Rupert and
Wisthaler, Armin and Kiendler-Scharr, Astrid},
title = {{C}omparison of three aerosol chemical characterization
techniques utilizing {PTR}-{T}o{F}-{MS}: {A} study on
freshly formed and aged biogenic {SOA}},
journal = {Atmospheric measurement techniques discussions},
volume = {288},
issn = {1867-8610},
address = {Katlenburg-Lindau},
publisher = {Copernicus},
reportid = {FZJ-2017-07270},
pages = {1 - 31},
year = {2017},
abstract = {An inter-comparison of different aerosol chemical
characterization techniques has been performed as part of a
chamber study of biogenic SOA formation and aging at the
atmosphere simulation chamber SAPHIR. Three different
aerosol sampling techniques, the aerosol collection module
(ACM), the chemical analysis of aerosol on-line (CHARON) and
the collection thermal desorption unit (TD) were connected
to Proton Transfer Reaction Time of Flight Mass
Spectrometers (PTR-ToF-MS) to provide chemical
characterization of the SOA. The techniques were compared
among each other and to results from an Aerosol Mass
Spectrometer (AMS) and a Scanning Mobility Particle Sizer
(SMPS). The experiments investigated SOA formation from the
ozonolysis of β-pinene, limonene, a β-pinene/limonene mix
and real plant emissions from Pinus sylvestris L. (Scots
pine). The SOA was subsequently aged by photooxidation
except for limonene SOA which was aged by NO3
oxidation.Despite significant differences in the aerosol
collection and desorption methods of the PTR based
techniques, the determined chemical composition, i.e. the
same major contributing signals were found by all
instruments for the different chemical systems studied.
These signals could be attributed to known products expected
from the oxidation of the examined monoterpenes. The
sampling and desorption method of ACM and TD, provided
additional information on the volatility of individual
compounds and showed relatively good agreement.Averaged over
all experiments, the total aerosol mass recovery compared to
an SMPS varied from $80 ± 10 \%,$ $51 ± 5 \%$
and $27 ± 3 \%$ for CHARON, ACM and TD, respectively.
Comparison to the oxygen to carbon ratios (O : C)
obtained by AMS showed that all PTR based techniques
observed lower O : C ratios indicating a loss of
molecular oxygen either during aerosol sampling or
detection. The differences in total mass recovery and
O : C between the three instruments resulted
predominately from differences in the field strength (E/N)
in the drift-tube reaction ionization chambers of the
PTR-ToF-MS instruments and from dissimilarities in the
collection/desorption of aerosols. Laboratory case studies
showed that PTR-ToF-MS E/N conditions influenced
fragmentation which resulted in water loss and carbon-oxygen
bond breakage of the detected molecules. Since ACM and TD
were operated in higher E/N compared to CHARON this resulted
to higher fragmentation, thus affecting primarily the
detected oxygen and carbon content and therefore also the
mass recovery. Overall, these techniques have been shown to
provide valuable insight on the chemical characteristics of
BSOA, and can address unknown thermodynamic properties such
as partitioning coefficient values and volatility patterns
down to a compound specific level.},
cin = {IEK-8},
ddc = {550},
cid = {I:(DE-Juel1)IEK-8-20101013},
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},
doi = {10.5194/amt-2017-288},
url = {https://juser.fz-juelich.de/record/838710},
}