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Products of Criegee intermediate reactions with NO2: experimental measurements and tropospheric implications
Author(s) -
Rebecca L. Caravan,
M. Anwar H. Khan,
Brandon Rotavera,
Ewa Papajak,
Ivan O. Antonov,
Mingwei Chen,
Kendrew Au,
Wen Chao,
David L. Osborn,
Jim J. Lin,
Carl J. Percival,
Dudley E. Shallcross,
Craig A. Taatjes
Publication year - 2017
Publication title -
faraday discussions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.255
H-Index - 110
eISSN - 1364-5498
pISSN - 1359-6640
DOI - 10.1039/c7fd00007c
Subject(s) - chemistry , adduct , acetaldehyde , formaldehyde , ozone , yield (engineering) , oxide , atmospheric chemistry , reactivity (psychology) , photochemistry , computational chemistry , organic chemistry , thermodynamics , ethanol , medicine , physics , alternative medicine , pathology
The reactions of Criegee intermediates with NO 2 have been proposed as a potentially significant source of the important nighttime oxidant NO 3 , particularly in urban environments where concentrations of ozone, alkenes and NO x are high. However, previous efforts to characterize the yield of NO 3 from these reactions have been inconclusive, with many studies failing to detect NO 3 . In the present work, the reactions of formaldehyde oxide (CH 2 OO) and acetaldehyde oxide (CH 3 CHOO) with NO 2 are revisited to further explore the product formation over a pressure range of 4-40 Torr. NO 3 is not observed; however, temporally resolved and [NO 2 ]-dependent signal is observed at the mass of the Criegee-NO 2 adduct for both formaldehyde- and acetaldehyde-oxide systems, and the structure of this adduct is explored through ab initio calculations. The atmospheric implications of the title reaction are investigated through global modelling.

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