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Hygroscopic properties of newly formed ultrafine particles at an urban site surrounded by deciduous forest (Sapporo, northern Japan) during the summer of 2011

机译:2011年夏季,落叶林(北日本北部札幌,日本札幌,日本札幌,日本札幌)的新成型超细颗粒的吸湿性

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To investigate the hygroscopic properties of ultrafine particles during new particle formation events, the hygroscopic growth factors of size-segregated atmospheric particles were measured at an urban site in Sapporo, northern Japan, during the summer of 2011. The hygroscopic growth factor at 85 % relative humidity [g(85%)] of freshly formed nucleation mode particles was 1.11 to 1.28 (average: 1.16 ± 0.06) at a dry particle diameter (Dp) centered on 20 nm, which is equivalent to 1.17 to 1.35 (1.23 ± 0.06) at a dry Dp centered on 100 nm after considering the Kelvin effect. These values are comparable with those of secondary organic aerosols, suggesting that low-volatility organic vapors are important to the burst of nucleation mode particles. The equivalent g(85%) at a dry Dp of 100 nm for nucleated particles that have grown to Aitken mode sizes (1.24 to 1.34; average: 1.30 ± 0.04) were slightly higher than those of newly formed nucleation mode particles, suggesting that the growth of freshly formed nucleation mode particles to the Aitken mode size can be subjected to condensation of not only low-volatility organic vapors, but also water-soluble inorganic species. Based on this result, and previous measurement of radiocarbon in aerosols, we suggest that the burst of nucleation mode particles and their subsequent growth were highly affected by biogenic organic emissions at this measurement site, which is surrounded by deciduous forest. Gradual increases in mode diameter after the burst of nucleation mode particles were observed under southerly wind conditions, with a dominant contribution of intermediately hygroscopic particles. However, sharp increases in mode diameter were observed when the wind direction shifted to northwesterly or northeasterly, with a sharp increase in the highly hygroscopic particle fraction of the Aitken mode particles, indicating that the hygroscopic growth factor of newly formed particles is perturbed by the local winds that deliver different air masses to the measurement site.
机译:为了研究新的颗粒形成事件期间超细颗粒的吸湿性,在2011年夏季,在日本北部的札幌市札幌市札幌的城市遗址测量了尺寸隔离的大气颗粒的吸湿生长因子。相对的85%的吸湿生长因子在20nm的干粒径(DP)的干粒径(DP)下湿度[g(85%)]在20nm的干燥粒径(dp)下为1.11至1.28),其相当于1.17至1.35(1.23±0.06)在考虑到开尔文效应后,在一个处于100nm的干燥DP。这些值与二次有机气溶胶的相当,表明低挥发性有机蒸气对核切割模式颗粒的爆发很重要。在100nm的干燥DP的等效G(85%)对于已经生长到AITKEN模式尺寸的核(1.24至1.34;平均:1.30±0.04)略高于新形成的成核模式颗粒,表明新成形的核切割模式颗粒的生长可以对αEITKEN模式颗粒进行凝聚不仅是低挥发性有机蒸气,而且还可以进行水溶性无机物种。基于该结果,先前测量气溶胶中的radiocarbon,我们建议核心模式颗粒的爆发及其随后的生长受到该测量部位的生物有机排放的高度影响,这些测量部位被落叶林包围。在横向风条件下观察到成核模式颗粒突发后模式直径的逐渐增加,具有中间吸湿颗粒的显着贡献。然而,当风向转移到西北或东北部的风向时,观察到模式直径的急剧增加,随着AITKEN模式颗粒的高湿粒子分数急剧增加,表明新形成的颗粒的吸湿生长因子被局部扰动向测量部位提供不同的空气肿块的风。

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