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RESEARCH ARTICLE

Secondary organic aerosol tracers and malic acid in Hong Kong: seasonal trends and origins

Di Hu A B D and Jian Zhen Yu C
+ Author Affiliations
- Author Affiliations

A Department of Chemistry, Hong Kong Baptist University, Kowloon Tong, Kowloon, Hong Kong, P. R. China.

B HKBU Institute of Research and Continuing Education, Shenzhen Virtual University Park, Shenzhen, 518057, P. R. China.

C Department of Chemistry and Division of Environment, Hong Kong University of Science & Technology, Clear Water Bay, Kowloon, Hong Kong, P. R. China.

D Corresponding author. Email: dihu@hkbu.edu.hk

Environmental Chemistry 10(5) 381-394 https://doi.org/10.1071/EN13104
Submitted: 5 June 2013  Accepted: 26 August 2013   Published: 22 October 2013

Environmental context. Secondary organic aerosols (SOAs), a major organic component of ambient fine particles, contribute to adverse health effects and visibility degradation. Quantification of SOA tracers allows estimation of contributions from specific precursors, which helps the formulation of effective control strategies. We found that malic acid was present in SOA at high abundance in both winter and summer; its seasonally distinct inter-species relationships offer insights into distinct SOA formation pathways.

Abstract. Fine particle samples collected at an urban location in Hong Kong during winter were analysed by gas chromatography–ion trap mass spectrometry with prior chemical derivatisation. In total, 15 secondary organic aerosol (SOA) tracers from isoprene, monoterpenes, β-caryophyllene and toluene, and 24 other polar oxygenated compounds, were identified and quantified. Monoterpenes and isoprene SOA tracers showed lower levels on winter long-range transport (LRT) days than summer regional days, the latter being reported in our previous study. Opposite seasonal trends were observed for SOA tracers of β-caryophyllene and toluene. The averaged total secondary organic carbon (SOC) apportioned to these four volatile organic compounds (VOCs) was estimated to be 4.73 μg C m–3 on winter LRT days, lower than that on summer regional days (5.21 μg C m–3). β-caryophyllene and monoterpenes were found to be the most significant SOC contributors to PM2.5 in Hong Kong in both winter and summer, and their averaged SOC contributions on winter LRT days were 2.24 and 1.59 μg C m–3. Toluene and isoprene had relatively minor contributions to SOC in Hong Kong in both seasons, with averaged SOC contributions of 0.81 and 0.08 μg C m–3 on winter LRT days. Malic acid was well correlated with biogenic SOA tracers and oxalate in both seasons, whereas correlation between malic and succinic acid was only found in winter. Based on the seasonal characteristic inter-species correlations in the region, we hypothesise that malic acid could be formed mainly by the aqueous-phase photodegradation of SOA products of biogenic VOCs during summer. In winter, emissions of biogenic VOCs are greatly reduced and succinic acid then becomes the predominant contributor to malic acid.


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