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Absorption properties and size distribution of aerosol particles during the fall season at an urban site of Gwangju, Korea

机译:韩国光州市区秋季秋季气溶胶颗粒的吸收特性和粒径分布

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摘要

To investigate the influence of pollution events on the chemical composition and formation processes of aerosol particles, 24-h integrated size-segregated particulate matter (PM) was collected during the fall season at an urban site of Gwangju, Korea and was used to determine the concentrations of mass, water-soluble organic carbon (VVSOC) and ionic species. Furthermore, black carbon (BC) concentrations were observed with an aethalometer. The entire sampling period was classified into four periods, i.e., typical, pollution event I, pollution event Ⅱ, and an Asian dust event. Stable meteorological conditions (e.g., low wind speed, high surface pressure, and high relative humidity) observed during the two pollution events led to accumulation of aerosol particles and increased formation of secondary organic and inorganic aerosol species, thus causing PM_(2.5) increase. Furthermore, these stable conditions resulted in the predominant condensation or droplet mode size distributions of PM, WSOC, NO_3~-, and SO_4~(2-). However, difference in the accumulation mode size distributions of secondary water-soluble species between pollution events Ⅰ and Ⅱ could be attributed to the difference in transport pathways of air masses from high-pollution regions and the formation processes for the secondary chemical species. The average absorption Angstrom exponent (AAE_(370-950)) for 370-950 nm wavelengths > 1.0 indicates that the BC particles from traffic emissions were likely mixed with light absorbing brown carbon (BrC) from biomass burning (BB) emissions. It was found that light absorption by BrC in the near UV range was affected by both secondary organic aerosol and BB emissions. Overall, the pollution events observed during fall at the study site can be due to the synergy of unfavorable meteorological conditions, enhanced secondary formation, local emissions, and long-range transportation of air masses from upwind polluted areas.
机译:为了调查污染事件对气溶胶颗粒化学成分和形成过程的影响,在秋季期间,在韩国光州的一个城市地点收集了24小时的尺寸分离的颗粒物(PM),用于确定污染物的浓度。质量浓度,水溶性有机碳(VVSOC)和离子种类。此外,用电量计观察到黑碳(BC)浓度。整个采样期分为四个时期,即典型的污染事件I,污染事件Ⅱ和亚洲粉尘事件。在这两次污染事件中观察到的稳定的气象条件(例如低风速,高表面压力和高相对湿度)导致气溶胶颗粒堆积,并增加了有机和无机次级气溶胶物种的形成,从而导致PM_(2.5)增加。此外,这些稳定条件导致了PM,WSOC,NO_3〜-和SO_4〜(2-)的主要冷凝或液滴模式尺寸分布。然而,污染事件Ⅰ和Ⅱ之间次要水溶性物质的积累模式大小分布的差异可能是由于高污染区空气团的输送途径和次要化学物质形成过程的不同所致。波长大于1.0的370-950 nm处的平均吸收埃指数(AAE_(370-950))表明,来自交通排放的BC颗粒可能与吸收来自生物质燃烧(BB)排放的棕色碳(BrC)混合在一起。已经发现,BrC在近紫外线范围内的光吸收受到次级有机气溶胶和BB排放的影响。总体而言,在研究地点坠落期间观察到的污染事件可能是由于不利的气象条件,增强的次生形成,局部排放以及来自上风污染区的气团的远距离运输的协同作用所致。

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