Synthesis and characterisation of peroxypinic acids as proxies for highly oxygenated molecules (HOMs) in secondary organic aerosol

• Published in: Atmospheric chemistry and physics Vol. 18; no. 15; pp. 10973 - 10983
• Main Authors: Steimer, Sarah S, Delvaux, Aurélie, Campbell, Steven J, Gallimore, Peter J, Grice, Peter, Howe, Duncan J, Pitton, Dominik, Claeys, Magda, Hoffmann, Thorsten, Kalberer, Markus
• Format: Journal Article
• Language: English
• Published: Katlenburg-Lindau Copernicus GmbH 06.08.2018; Copernicus Publications
• Subjects: Acids; Aerosols; Analytical methods; Atmospheric processes; Chemical properties; Chemical synthesis; Chromatography; Detection; Environmental aspects; Humidity; Laboratory experiments; Liquid chromatography; Mass spectrometry; Mass spectroscopy; Ozonolysis; Particle formation; Secondary aerosols; Timing; Toxicity; α-Pinene
• ISSN: 1680-7324; 1680-7316; 1680-7324
• DOI: 10.5194/acp-18-10973-2018

Peroxy acids were recently found to be involved in new particle formation in the atmosphere and could also substantially contribute towards particle toxicity. However, a lack of suitable analytical methods for the detection and characterisation of peroxy acids in the particle phase is currently hindering the quantitative investigation of their contribution to these important atmospheric processes. Further development of appropriate techniques and relevant standards is therefore urgently needed. In this study, we synthesised three peroxypinic acids, developed a liquid chromatography separation method and characterised them with tandem mass spectrometry. The observed fragmentation patterns clearly distinguish the different peroxypinic acids from both the acid and each other, showing several neutral losses previously already observed for other peroxy acids. Both monoperoxypinic acids were found to be present in secondary organic aerosol generated from ozonolysis of α-pinene in laboratory experiments. The yield of monoperoxypinic acid formation was not influenced by humidity. Monoperoxypinic acid quickly degrades on the filter, with about 60 % lost within the first 5 h. This fast degradation shows that time delays in traditional off-line analysis will likely lead to severe underestimates of peroxy compound concentrations in ambient particles.