4.7 Article

Impact of pyruvic acid photolysis on acetaldehyde and peroxy radical formation in the boreal forest: theoretical calculations and model results

Journal

ATMOSPHERIC CHEMISTRY AND PHYSICS
Volume 21, Issue 18, Pages 14333-14349

Publisher

COPERNICUS GESELLSCHAFT MBH
DOI: 10.5194/acp-21-14333-2021

Keywords

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Funding

  1. ENVRIplus [654182]
  2. ENVRIplus of the IBAIRN campaign

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By measuring gas-phase pyruvic acid in the boreal forest, the impact of its photolysis on the formation of acetaldehyde and peroxy radicals was studied. The results show that the photolysis of pyruvic acid is a significant source of acetaldehyde and acetylperoxy radicals.
Based on the first measurements of gas-phase pyruvic acid (CH3C(O)C(O)OH) in the boreal forest, we derive effective emission rates of pyruvic acid and compare them with monoterpene emission rates over the diel cycle. Using a data-constrained box model, we determine the impact of pyruvic acid photolysis on the formation of acetaldehyde (CH3CHO) and the peroxy radicals CH3C(O)O-2 and HO2 during an autumn campaign in the boreal forest. The results are dependent on the quantum yield (phi) and mechanism of the photodissociation of pyruvic acid and the fate of a likely major product, methylhydroxy carbene (CH3COH). With the box model, we investigate two different scenarios in which we follow the present IUPAC (IUPAC Task Group on Atmospheric Chemical Kinetic Data Evaluation, 2021) recommendations with phi = 0.2 (at 1 bar of air), and the main photolysis products (60 %) are acetaldehyde + CO2 with 35 % C-C bond fission to form HOCO and CH3CO (scenario A). In the second scenario (B), the formation of vibrationally hot CH3COH (and CO2) represents the main dissociation pathway at longer wavelengths (similar to 75 %) with a similar to 25 % contribution from C-C bond fission to form HOCO and CH3CO (at shorter wavelengths). In scenario 2 we vary phi between 0.2 and 1 and, based on the results of our theoretical calculations, allow the thermalized CH3COH to react with O-2 (forming peroxy radicals) and to undergo acid-catalysed isomerization to CH3CHO. When constraining the pyruvic acid to measured mixing ratios and independent of the model scenario, we find that the photolysis of pyruvic acid is the dominant source of CH3CHO with a contribution between similar to 70 % and 90 % to the total production rate. We find that the photolysis of pyruvic acid is also a major source of the acetylperoxy radical, with contributions varying between similar to 20 % and 60 % dependent on the choice of phi and the products formed. HO2 production rates are also enhanced, mainly via the formation of CH3O2. The elevated production rates of CH3C(O)O-2 and HO2 and concentration of CH3CHO result in significant increases in the modelled mixing ratios of CH3C(O)OOH, CH3OOH, HCHO, and H2O2.

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