TY  - JOUR
AU  - Rolletter, Michael
AU  - Kaminski, Martin
AU  - Acir, Ismail-Hakki
AU  - Bohn, Birger
AU  - Dorn, Hans-Peter
AU  - Li, Xin
AU  - Lutz, Anna
AU  - Nehr, Sascha
AU  - Rohrer, Franz
AU  - Tillmann, Ralf
AU  - Wegener, Robert
AU  - Hofzumahaus, Andreas
AU  - Kiendler-Scharr, Astrid
AU  - Wahner, Andreas
AU  - Fuchs, Hendrik
TI  - Investigation of the α -pinene photooxidation by OH in the atmospheric simulation chamber SAPHIR
JO  - Atmospheric chemistry and physics
VL  - 19
IS  - 18
SN  - 1680-7324
CY  - Katlenburg-Lindau
PB  - EGU
M1  - FZJ-2019-04919
SP  - 11635 - 11649
PY  - 2019
AB  - The photooxidation of the most abundant monoterpene, α-pinene, by the hydroxyl radical (OH) was investigated at atmospheric concentrations in the atmospheric simulation chamber SAPHIR. Concentrations of nitric oxide (NO) were below 120 pptv. Yields of organic oxidation products are determined from measured time series giving values of 0.11±0.05, 0.19±0.06, and 0.05±0.03 for formaldehyde, acetone, and pinonaldehyde, respectively. The pinonaldehyde yield is at the low side of yields measured in previous laboratory studies, ranging from 0.06 to 0.87. These studies were mostly performed at reactant concentrations much higher than observed in the atmosphere. Time series of measured radical and trace-gas concentrations are compared to results from model calculations applying the Master Chemical Mechanism (MCM) 3.3.1. The model predicts pinonaldehyde mixing ratios that are at least a factor of 4 higher than measured values. At the same time, modeled hydroxyl and hydroperoxy (HO2) radical concentrations are approximately 25 % lower than measured values. Vereecken et al. (2007) suggested a shift of the initial organic peroxy radical (RO2) distribution towards RO2 species that do not yield pinonaldehyde but produce other organic products. Implementing these modifications reduces the model–measurement gap of pinonaldehyde by 20 % and also improves the agreement in modeled and measured radical concentrations by 10 %. However, the chemical oxidation mechanism needs further adjustment to explain observed radical and pinonaldehyde concentrations. This could be achieved by adjusting the initial RO2 distribution, but could also be done by implementing alternative reaction channels of RO2 species that currently lead to the formation of pinonaldehyde in the model.
LB  - PUB:(DE-HGF)16
UR  - <Go to ISI:>//WOS:000486704600001
DO  - DOI:10.5194/acp-19-11635-2019
UR  - https://juser.fz-juelich.de/record/865539
ER  -