TY  - JOUR
AU  - Karl, M.
AU  - Dye, C.
AU  - Schmidbauer, N.
AU  - Wisthaler, A.
AU  - Mikoviny, T.
AU  - D'Anna, B.
AU  - Müller, M.
AU  - Borrás, E.
AU  - Clemente, E.
AU  - Munoz, A.
AU  - Porras, R.
AU  - Ródenas, M.
AU  - Vázquez, M.
AU  - Brauers, T.
TI  - Study of OH-initiated degradation of 2-aminoethanol
JO  - Atmospheric chemistry and physics
VL  - 12
SN  - 1680-7316
CY  - Katlenburg-Lindau
PB  - EGU
M1  - PreJuSER-20324
SP  - 1881 - 1901
PY  - 2012
N1  - The Instituto Universitario CEAM-UMH is partly supported by Generalitat Valenciana, Fundacion Bancaja, and the projects GRACCIE (Consolider-Ingenio 2010) and FEEDBACKS (Prometeo - Generalitat Valenciana). The EUPHORE team is acknowledged for their support in the use of the facilities. Armin Wisthaler and Tomas Mikoviny acknowledge support from A. Hansel and T. D. Mark. Claus Nielsen is thanked for the preparation of the reference salt, ethanolaminium nitrate, for the AMS analysis. Eldbjorg S. Heimstad and Mikael Harju (NILU Tromso) are thanked for determination of rate constants of several products from OH-initiated oxidation of MEA using EPI Suite version 4.0.
AB  - The degradation of 2-aminoethanol (MEA) by the hydroxyl radical (OH) was studied in the European Photoreactor (EUPHORE), a large outdoor environmental chamber. High-Temperature Proton-Transfer-Reaction Mass Spectrometry (HT-PTR-MS) and Fast Fourier Transform Infrared (FT-IR) were used to follow concentrations of reactants in the gas phase. Aerosol mass concentrations were tracked with Aerosol Mass Spectrometry (AMS). The chamber aerosol model MAFOR was applied to quantify losses of MEA to the particle phase. The rate constant k(OH + MEA) was determined relative to the rate constant of the 1,3,5-trimethylbenzene reaction with OH and was found to be (9.2 +/- 1.1) x 10(-11) cm(3) molecule(-1) s(-1), and thus the reaction between OH radicals and MEA proceeds a factor of 2-3 faster than estimated by structure-activity relationship (SAR) methods. Main uncertainty of the relative rate determination is the unknown temporal behaviour of the loss rate of MEA to chamber wall surfaces during the sunlit experiments. Nucleation and growth of particles observed in the experiments could be reproduced by the chamber model that accounted for condensation of gaseous oxidation products, condensation of ethanolaminium nitrate and nucleation involving MEA and nitric acid.
KW  - J (WoSType)
LB  - PUB:(DE-HGF)16
UR  - <Go to ISI:>//WOS:000300875900014
DO  - DOI:10.5194/acp-12-1881-2012
UR  - https://juser.fz-juelich.de/record/20324
ER  -