Index Geophysics

α-pinene photooxidation under controlled chemical conditions – Part 1: Gas-phase composition in low- and high-NOx environments

The OH oxidation of α-pinene under both low- and high-NO_x environments was studied in the Caltech atmospheric chambers. Ozone was kept low to ensure OH was the oxidant. The initial α-pinene concentration was 20–50 ppb to ensure that the dominant peroxy radical pathway under low-NO_x conditions is reaction with HO₂, produced from reaction of OH with H₂O₂, and under high-NO_x conditions, reactions with NO. Here we present the gas-phase results observed. Under low-NO_x conditions the main first generation oxidation products are a number of α-pinene hydroxy hydroperoxides and pinonaldehyde, accounting for over 40% of the yield. In all, 65–75% of the carbon can be accounted for in the gas phase; this excludes first-generation products that enter the particle phase. We suggest that pinonaldehyde forms from RO₂ + HO₂ through an alkoxy radical channel that regenerates OH, a mechanism typically associated with acyl peroxy radicals, not alkyl peroxy radicals. The OH oxidation and photolysis of α-pinene hydroxy hydroperoxides leads to further production of pinonaldehyde, resulting in total pinonaldehyde yield from low-NO_x OH oxidation of ~33%. The low-NO_x OH oxidation of pinonaldehyde produces a number of carboxylic acids and peroxyacids known to be important secondary organic aerosol components. Under high-NO_x conditions, pinonaldehyde was also found to be the major first-generation OH oxidation product. The high-NO_x OH oxidation of pinonaldehyde did not produce carboxylic acids and peroxyacids. A number of organonitrates and peroxyacyl nitrates are observed and identified from α-pinene and pinonaldehyde.

Eddingsaas, N. C.

Loza, C. L.

Yee, L. D.

Seinfeld, J. H.

Wennberg, P. O.

2018-01-15

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10.5194/acp-12-6489-2012

https://acp.copernicus.org/articles/12/6489/2012/

eISSN: 1680-7324

eng