1. Concentration and size distribution of water-extracted dimethylaminium and trimethylaminium in atmospheric particles during nine campaigns - Implications for sources, phase states and formation pathways.
- Author
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Xie, Huan, Feng, Limin, Hu, Qingjing, Zhu, Yujiao, Gao, Huiwang, Gao, Yang, and Yao, Xiaohong
- Subjects
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METHYL groups , *BIOCONCENTRATION , *MARINE pollution , *PARTICLE size distribution , *BEACHES - Abstract
In this study, we determined the concentrations of water-extracted dimethylaminium (DMA + ) and trimethylaminium (TMA + ) in size-segregated atmospheric particles collected during three inland campaigns and one sea-beach campaign in Qingdao and five marine campaigns in marginal seas of China and the northwest Pacific Ocean. The averages of DMA + and TMA + in PM 0.056 – 10 (the sum of concentrations from 0.056 to 10 μm) during each campaign ranged from 0.045 to 1.1 nmol m −3 and from 0.029 to 0.53 nmol m −3 , respectively. The increased concentrations of DMA + and TMA + in PM 0.056 – 10 , particularly the 1–2 orders of magnitude increased ratios of DMA + /NH 4 + and TMA + /NH 4 + , in the marine and sea-beach atmospheres indicated that the overwhelming majority was derived from marine sources. Size distributions of TMA + and DMA + were also investigated in terms of phase states and formation pathways, e.g., the dominant modes of particulate DMA + and TMA + in some samples were characterized by the mass median aerodynamic diameter at 0.1–0.2 μm against the dominant mode of NH 4 + and SO 4 2− at 0.7–0.9 μm, while the ratios of DMA + /NH 4 + and/or TMA + /NH 4 + in <0.2 μm particles increased by 3–10 times from the corresponding lower values in >0.2 μm particles. This strongly implied that the particulate DMA + and TMA + at <0.2 μm size range overwhelmingly existed in the liquid organic phase as unprotonated TMA and DMA, but those at the >0.2 μm size range mainly existed in the aqueous (or solid) phase where the dominance of gas-aerosol equilibria would cause the ratios to be almost size-independent. The size-dependent phase states corresponded to their various formation pathways. [ABSTRACT FROM AUTHOR]
- Published
- 2018
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