4.7 Article

Molecular distributions of dicarboxylic acids, oxocarboxylic acids, and α-dicarbonyls in aerosols over Tuoji Island in the Bohai Sea: Effects of East Asian continental outflow

期刊

ATMOSPHERIC RESEARCH
卷 272, 期 -, 页码 -

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.atmosres.2022.106154

关键词

Water-soluble SOA; East Asian continental outflow; Molecular characteristics; Source identification; Photochemical aging; Biomass burning

资金

  1. National Natural Science Foundation of China [21577079]
  2. Japan Society for the Promotion of Science (JSPS) [24221001]
  3. Jiangsu Collaborative Innovation Center for Climate Change
  4. China Scholarship Council (CSC)

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Field measurements of dicarboxylic acids and related compounds in PM2.5 were conducted in Tuoji Island, China. The concentrations were found to be strongly influenced by the East Asian continental outflow and the air parcel's residence time in the polluted boundary layer. The results also revealed that secondary sources were dominant, while biomass and plastic waste burning were significant primary sources.
Field measurements of the concentrations of dicarboxylic acids and related compounds (oxocarboxylic acids and a-dicarbonyls) in PM2.5 were conducted on a background island (Tuoji Island, China) over the Bohai Sea to better understand the effects of pollution downwind of the East Asian continental outflow. Air mass backward trajectory calculations demonstrated that the distributions of dicarboxylic acids and related compounds at Tuoji Island depended strongly on the East Asian continental outflow and correlated with the hours spent by an air parcel in the polluted boundary layer. Based on the data analysis, the sampling period was categorized into heavy aerosol pollution periods (HAPPs) and light aerosol pollution periods (LAPPs). The average concentration of dicarboxylic acids and related compounds during HAPPs (1280 +/- 503 ng m(-3)) was approximately seven times higher than that during LAPPs (189 +/- 90.8 ng m(-3)). The order of the major species of dicarboxylic acids and related compounds, ranked by concentrations, was oxalic acid (C-2) > glyoxylic acid (omega C-2) > succinic acid (C-4) > terephthalic acid (tPh) during HAPPs, and C-2 > malonic acid (C-3) >omega C-2 > C-4 during LAPPs. Results of positive matrix factorization (PMF) showed that secondary sources were the dominant source of dicarboxylic acids and related compounds, with contributions of 38% and 57% during HAPPs and LAPPs, respectively. Primary sources of biomass burning and plastic waste burning were also significant during HAPPs (contributions: 26% and 20%, respectively) and LAPPs (contributions: 18% and 12%, respectively). The concentration ratios of C-3 to C-4 (C-3/C-4), C-2 to C-4 (C-2/C-4), fumaric acid to maleic acid (F/M), phthalic acid to azelaic acid (Ph/C-9), adipic acid to azelaic acid (C-6/C-9), and the positive correlations of Ph or tPh with dicarboxylic acids, and levoglucosan with dicarboxylic acids and related compounds further support the PMF results.

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