2018
DOI: 10.1016/j.scitotenv.2018.02.303
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Concentration and size distribution of water-extracted dimethylaminium and trimethylaminium in atmospheric particles during nine campaigns - Implications for sources, phase states and formation pathways

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Cited by 30 publications
(59 citation statements)
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“…In four out of the five total samples in Category 2, the concentrations of NH 4 + , NO 3 − , and SO 4 − in PM 0.056–10 are significantly smaller than the 66th percentile values of the corresponding species in Categories 1 and 3. In addition, the ratios of [TMA + ] PM0.056–10 /[NH 4 + ] PM0.056–10 and [DMA + ] PM0.056–10 /[NH 4 + ] PM0.056–10 in Category 2 are approximately 1 order of magnitude larger than those observed at a semiurban site along the coast of the SYS (Xie et al, ). These results imply that the DMA + and TMA + in PM 0.056–10 may be derived mainly from oceanic sources rather than long‐range transport from continental sources.…”
Section: Resultsmentioning
confidence: 97%
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“…In four out of the five total samples in Category 2, the concentrations of NH 4 + , NO 3 − , and SO 4 − in PM 0.056–10 are significantly smaller than the 66th percentile values of the corresponding species in Categories 1 and 3. In addition, the ratios of [TMA + ] PM0.056–10 /[NH 4 + ] PM0.056–10 and [DMA + ] PM0.056–10 /[NH 4 + ] PM0.056–10 in Category 2 are approximately 1 order of magnitude larger than those observed at a semiurban site along the coast of the SYS (Xie et al, ). These results imply that the DMA + and TMA + in PM 0.056–10 may be derived mainly from oceanic sources rather than long‐range transport from continental sources.…”
Section: Resultsmentioning
confidence: 97%
“…In the measurements collected from the marginal seas of China to the NWPO in the spring of 2015, the dominant modes of DMA + and TMA + are generally resolved at 0.4 ± 0.1 μm; on a few occasions, they are resolved at 0.8 ± 0.2 μm (Yu et al, ). In the literature, the particle mode of species at 0.4 μm may be associated with either primary combustion emissions or heterogeneous reactions (Ondov & Wexler, ; Xie et al, ). Assuming that the DMA + over the NWPO is derived mainly from oceanic sources, the latter likely formed the DMA + mode at 0.4 ± 0.1 μm through an acid‐base neutralization reaction between the gaseous amines and acidic particles (Sauerwein & Chan, ; Xie et al, ).…”
Section: Resultsmentioning
confidence: 99%
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