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Updated: Jan 20, 2026

Direct Analysis of Single Cells by Mass Spectrometry at Atmospheric Pressure
Published on: September 4, 2010
Does atmospheric processing produce toxic Pb-containing compounds? A case study in suburban Beijing by single
Long Peng1, Lei Li2, Qinhao Lin3
1State Key Laboratory of Organic Geochemistry and Guangdong Provincial Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, PR China; University of Chinese Academy of Sciences, Beijing, 100049, PR China.
Abstract:
A single particle aerosol mass spectrometry (SPAMS) was deployed to investigate the mixing state and chemical processing of Pb-rich particles in suburban Beijing. Based on a large dataset of mass spectra, Pb-rich particles were classified into Pb-O-Cl-N-S (55%), Pb-N (17%), Pb-N-S (15%), and Pb-EC (7%). Residual coal combustion, industrial activities, and meteorological conditions were identified as main factors regulating the variations of Pb-rich particles in the atmosphere. The highest abundance of the Pb-rich particles was observed during heating period (HP) primarily due to the increase in coal usage. Pb in Pb-O-Cl-N-S type was identified in forms of PbO, PbCl2, and Pb(NO3)2. Dominantly presented in the form of Pb(NO3)2, Pb-N type represented the completely transformed Pb-rich particles from PbO/PbCl2 by atmospheric processes. It is found that PbCl2 and PbO could be transformed to Pb(NO3)2, highly dependent on the amount of NO2 and RH. Significant enhancement of nitrate in Pb-O-Cl-N-S particles was observed when the RH was greater than 60%, emphasizing the importance of heterogeneous hydrolysis of N2O5 on the formation of Pb(NO3)2. Compared with non-carcinogenic PbCl2/PbO and insoluble PbO, soluble and carcinogenic Pb(NO3)2 produced by atmospheric processes may significantly enhance negative effects of Pb-rich particles on human health and the ecosystem.
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