Aarhus University Seal

Urban organic aerosol composition in eastern China differs from north to south: Molecular insight from a liquid chromatography-mass spectrometry (Orbitrap) study

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review


  • Kai Wang, Chinese Academy of Sciences, Johannes Gutenberg University Mainz
  • ,
  • Ru Jin Huang, Pilot National Laboratory for Marine Science and Technology (Qingdao), Chinese Academy of Sciences
  • ,
  • Martin Brüggemann, Leibniz Institute for Tropospheric Research
  • ,
  • Yun Zhang, Johannes Gutenberg University Mainz
  • ,
  • Lu Yang, Chinese Academy of Sciences
  • ,
  • Haiyan Ni, Chinese Academy of Sciences
  • ,
  • Jie Guo, Chinese Academy of Sciences
  • ,
  • Meng Wang, Chinese Academy of Sciences
  • ,
  • Jiajun Han, University of Toronto
  • ,
  • Merete Bilde
  • Marianne Glasius
  • Thorsten Hoffmann, Johannes Gutenberg University Mainz

Air pollution by particulate matter in China affects human health, the ecosystem and the climate. However, the chemical composition of particulate aerosol, especially of the organic fraction, is still not well understood. In this study, particulate aerosol samples with a diameter of ≤2.5g μm (PM2.5) were collected in January 2014 in three cities located in northeast, east and southeast China, namely Changchun, Shanghai and Guangzhou. Organic aerosol (OA) in the PM2.5 samples was analyzed by an ultrahigh-performance liquid chromatograph (UHPLC) coupled to a high-resolution Orbitrap mass spectrometer in both negative mode (ESI-) and positive mode electrospray ionization (ESI+). After non-target screening including the assignment of molecular formulas, the compounds were classified into five groups based on their elemental composition, i.e., CHO, CHON, CHN, CHOS and CHONS. The CHO, CHON and CHN groups present the dominant signal abundances of 81g %-99.7g % in the mass spectra and the majority of these compounds were assigned to mono- and polyaromatics, suggesting that anthropogenic emissions are a major source of urban OA in all three cities. However, the chemical characteristics of these compounds varied between the different cities. The degree of aromaticity and the number of polyaromatic compounds were substantially higher in samples from Changchun, which could be attributed to the large emissions from residential heating (i.e., coal combustion) during wintertime in northeast China. Moreover, the ESI- analysis showed higher H/C and O/C ratios for organic compounds in Shanghai and Guangzhou compared to samples from Changchun, indicating that OA undergoes more intense photochemical oxidation processes in lower-latitude regions of China and/or is affected to a larger degree by biogenic sources. The majority of sulfur-containing compounds (CHOS and CHONS) in all cities were assigned to aliphatic compounds with low degrees of unsaturation and aromaticity. Here again, samples from Shanghai and Guangzhou show a greater chemical similarity but differ largely from those from Changchun. It should be noted that the conclusions drawn in this study are mainly based on comparison of molecular formulas weighted by peak abundance and thus are associated with inherent uncertainties due to different ionization efficiencies for different organic species.

Original languageEnglish
JournalAtmospheric Chemistry and Physics
Pages (from-to)9089-9104
Number of pages16
Publication statusPublished - Jun 2021

    Research areas


See relations at Aarhus University Citationformats

ID: 221270241