Affiliation:
1. Institute of Surface‐Earth System Science, School of Earth System Science Tianjin University Tianjin China
2. Tianjin Bohai Rim Coastal Earth Critical Zone National Observation and Research Station Tianjin University Tianjin China
3. Haihe Laboratory of Sustainable Chemical Transformations Tianjin China
4. Bioanalytical Chemistry, Department of Chemistry Humboldt University Berlin Berlin Germany
Abstract
RationaleThe sources and chemical compositions of organic aerosol (OA) exert a significant influence on both regional and global atmospheric conditions, thereby having far‐reaching implications on environmental chemistry. However, existing mass spectrometry (MS) methods have limitations in characterizing the detailed composition of OA due to selective ionization as well as fractionation during cold‐water extraction and solid‐phase extraction (SPE).MethodsA comprehensive MS study was conducted using aerosol samples collected on dusty, clean, and polluted days. To supplement the data obtained from electrospray ionization (ESI), a strategy for analyzing OAs collected using the quartz fiber filter directly utilizing laser desorption ionization (LDI) was employed. Additionally, the ESI method was conducted to explore suitable approaches for determining various OA compositions from samples collected on dusty, clean, and polluted days.ResultsIn situ LDI has the advantages of significantly reducing the sample volume, simplifying sample preparation, and overcoming the problem of overestimating sulfur‐containing compounds usually encountered in ESI. It is suitable for the characterization of highly unsaturated and hydrophobic aerosols, such as brown carbon‐type compounds with low volatility and high stability, which is supplementary to ESI.ConclusionsCompared with other ionization methods, in situ LDI helps provide a complementary description of the molecular compositions of OAs, especially for analyzing OAs in polluted day samples. This method may contribute to a more comprehensive MS analysis of the elusive compositions and sources of OA in the atmosphere.
Funder
National Natural Science Foundation of China
State Key Laboratory of Heavy Oil Processing