Observations of Highly Oxidised Molecules and Particle Nucleation in the Atmosphere of Beijing
Preprint
- 27 March 2019
- preprint
- Published by Copernicus GmbH in EGUsphere
- Vol. 2019, 1-35
Abstract
Particle nucleation is one of the main sources of atmospheric particulate matter by number, with new particles having great relevance for human health and climate. Highly oxidised multifunctional organic molecules (HOMs) have been recently identified as key constituents in the growth, and, sometimes, in initial formation of new particles. While there have been many studies of HOMs in atmospheric chambers, flow tubes and clean environments, analyses of data from polluted environments are scarce. Here, measurements of HOMs and particle size distributions down to small molecular clusters are presented alongside VOC and trace gas data from a campaign in Beijing. Many gas phase HOMs have been characterised and their temporal trends and behaviours analysed in the context of new particle formation. The HOMs identified have a comparable degree of oxidation to those seen in other, cleaner, environments, likely due to an interplay between the higher temperatures facilitating rapid hydrogen abstractions and the higher concentrations of NOx and other RO2. terminators ending the autoxidation sequence more rapidly. Our data indicate that alkylbenzenes, monoterpenes, and isoprene are important precursor VOCs for HOMs in Beijing. Many of the C5 and C10 compounds derived from isoprene and monoterpenes have a slightly greater degree of average oxidation state of carbon compared to those from other precursors. Most HOMs except for large dimers have daytime peak concentrations, indicating the importance of OH. chemistry in the formation of HOMs, as O3 is lower on the days with higher HOM concentrations; similarly, VOC concentrations are lower on the days with higher HOM concentrations. The daytime peaks of HOMs coincide with the growth of freshly formed new particles, and their initial formation coincides with the peak in sulphuric acid vapours, suggesting that the nucleation process is sulphuric acid-dependent, with HOMs contributing to subsequent particle growth.Keywords
All Related Versions
- Published version: Atmospheric Chemistry and Physics, 19 (23), 14933.
This publication has 49 references indexed in Scilit:
- Atmospheric autoxidation is increasingly important in urban and suburban North AmericaProceedings of the National Academy of Sciences, 2017
- Formation of Highly Oxidized Radicals and Multifunctional Products from the Atmospheric Oxidation of AlkylbenzenesEnvironmental Science & Technology, 2017
- What Is Required for Highly Oxidized Molecules To Form Clusters with Sulfuric Acid?The Journal of Physical Chemistry A, 2017
- Thermodynamic properties of nanoparticles during new particle formation events in the atmosphere of North China PlainAtmospheric Research, 2017
- Elucidating severe urban haze formation in ChinaProceedings of the National Academy of Sciences, 2014
- Rapid Autoxidation Forms Highly Oxidized RO2 Radicals in the AtmosphereAngewandte Chemie International Edition, 2014
- Satellite methods underestimate indirect climate forcing by aerosolsProceedings of the National Academy of Sciences, 2011
- Competition of coagulation sink and source rate: New particle formation in the Pearl River Delta of ChinaAtmospheric Environment, 2010
- New particle formation in Beijing, China: Statistical analysis of a 1‐year data setJournal of Geophysical Research: Atmospheres, 2007
- Potential Role of Ultrafine Particles in Associations between Airborne Particle Mass and Cardiovascular HealthEnvironmental Health Perspectives, 2005