Isolating α‑Pinene Ozonolysis Pathways Reveals New Insights into Peroxy Radical Chemistry and Secondary Organic Aerosol Formation

• Published in: Environmental science & technology 2021-05, Vol.55 (10), p.6700-6709
• Main Authors: Zhao, Zixu, Zhang, Wen, Alexander, Taylor, Zhang, Xuan, Martin, David B. C, Zhang, Haofei
• Format: Article
• Language: English
• Subjects: Aerosols; Aldehydes; Anthropogenic Impacts on the Atmosphere; Atmosphere; Atmospheric conditions; Autoxidation; Carbonyl compounds; Carbonyls; Continuous flow; Continuously stirred tank reactors; Intermediates; Iodides; Ionic mobility; Ionization; Ions; Isomerization; Isomers; Mass spectrometry; Mass spectroscopy; Peroxy radicals; Scientific imaging; Spectroscopy; α-Pinene
• ISSN: 0013-936X; 1520-5851
• DOI: 10.1021/acs.est.1c02107

α-Pinene ozonolysis is a key process that impacts the formation of new particles and secondary organic aerosol (SOA) in the atmosphere. The mechanistic understanding of this chemistry has been inconclusive despite extensive research, hindering accurate simulations of atmospheric processes. In this work, we examine the ozonolysis of two synthesized unsaturated carbonyl isomers (C11H18O) which separately produce the two Criegee intermediates (CIs) that would form simultaneously in α-pinene ozonolysis. Direct gas-phase measurements of peroxy radicals (RO2) from flowtube ozonolysis experiments by an iodide-adduct chemical ionization mass spectrometer suggest that the initial C10H15O4 · RO2 from the CI with a terminal methyl ketone undergo autoxidation 20-fold faster than the CI with a terminal aldehyde and always outcompete the bimolecular reactions under typical laboratory and atmospheric conditions. These results provide experimental constraints on the detailed RO2 autoxidation mechanisms for understanding new particle formation in the atmosphere. Further, isomer-resolved characterization of the SOA formed from a continuous-flow stirred tank reactor using ion mobility spectrometry mass spectrometry suggests that the two structurally different CIs predominantly and unexpectedly form constituents with identical structures. These results open up possibilities of diverse isomerization pathways that the two CIs may undergo that form mutual products to a large extent toward their way forming the SOA. This work highlights new insights into α-pinene ozonolysis pathways and call for future studies to uncover the detailed mechanisms.