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Published on: March 18, 2019
[Concentrations and Size Distributions of Water-soluble Inorganic Ions in Aerosol Particles in Taiyuan, Shanxi]
Lu Wang1,2, Tian-Xue Wen1, Hong-Yan Miao1,3
1State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry(LAPC), Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, China.
Abstract:
Size-resolved filter samples were collected in Taiyuan every other week from June 2012 to May 2014. The mass concentrations of water-soluble ions (Na+, NH4+, K+, Mg2+, Ca2+, F-, Cl-, NO3- and SO42-) were measured by ion chromatography. The results showed that the total concentrations of measured water-soluble ions were (15.39±9.91), (21.10±15.49) and (36.34±18.51) μg·m-3 in PM1.1, PM2.1 and PM9, respectively. In PM1.1 and PM2.1, secondary water-soluble ions (SO42-, NO3- and NH4+) comprised 87.59% and 86.30% of all water-soluble ions, respectively, while in PM9, SO42- and Ca2+ comprised 32.78% and 28.54% of all water-soluble ions, respectively. SO42- and NH4+ had higher concentrations in winter and summer, and lower in spring and autumn. NO3-, K+and Cl- presented similar seasonal variation with a descending order of winter >autumn >spring >summer, and Ca2+ and Mg2+ followed the sequence of spring >winter >autumn >summer. SO42- and NH4+ showed a unimodal size distribution and the peak in the fine mode shifted from 0.43-0.65 μm in spring and autumn to 0.65-1.1 μm in summer. NO3- showed a bimodal size distribution. NO3- and NH4+ were dominated by the fine mode peaking at 0.43-2.1 μm in winter, and NO3- was dominated by the coarse mode peaking at 4.7-5.8 μm in summer. K+, Na+and Cl- also showed a bimodal size distribution with the fine mode at 0.43-1.1 μm and the coarse mode at 4.7-5.8 μm. Ca2+, Mg2+ and F- were unimodal with the peak in the coarse mode of 4.7-5.8 μm. On heavily polluted days, the mass concentrations of secondary water-soluble ions and Cl- accumulated, and secondary water-soluble ions were unimodal with the peak in the fine mode of 1.1-2.1 μm. However, on clear days, secondary water-soluble ions showed a bimodal size distribution with the fine mode at 0.43-0.65 μm and the coarse mode at 4.7-5.8 μm. The peak of secondary water-soluble ions in the fine mode shifted. PCA analysis showed that the sources of water-soluble ions were dominated by the secondary formation, coal combustion, industrial emission, biomass burning, and soil particles or falling dust.
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