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Photochemical aging of aerosol particles in different air masses arriving at Baengnyeong Island, Korea

机译:到达韩国班宁岛的不同气团中气溶胶颗粒的光化学老化

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Atmospheric aerosol particles are a serious health risk, especially in regions like East Asia. We investigated the photochemical aging of ambient aerosols using a potential aerosol mass?(PAM) reactor at Baengnyeong Island in the Yellow Sea during 4–12?August?2011. The size distributions and chemical compositions of aerosol particles were measured alternately every 6?min from the ambient air or through the highly oxidizing environment of a potential aerosol mass?(PAM) reactor. Particle size and chemical composition were measured by using the combination of a scanning mobility particle sizer?(SMPS) and a high-resolution time-of-flight aerosol mass spectrometer?(HR-ToF-AMS). Inside the PAM reactor, Osub3/sub and OH levels were equivalent to 4.6?days of integrated OH exposure at typical atmospheric conditions. Two types of air masses were distinguished on the basis of the chemical composition and the degree of aging: air transported from China, which was more aged with a higher sulfate concentration and O : C ratio, and the air transported across the Korean Peninsula, which was less aged with more organics than sulfate and a lower O : C ratio. For both episodes, the particulate sulfate mass concentration increased in the 200–400?nm size range when sampled through the PAM reactor. A decrease in organics was responsible for the loss of mass concentration in 100–200?nm particles when sampled through the PAM reactor for the organics-dominated episode. This loss was especially evident for the m∕z?43 component, which represents less oxidized organics. The m∕z?44 component, which represents further oxidized organics, increased with a shift toward larger sizes for both episodes. It is not possible to quantify the maximum possible organic mass concentration for either episode because only one OH exposure of 4.6?days was used, but it is clear that SOsub2/sub was a primary precursor of secondary aerosol in northeast Asia, especially during long-range transport from China. In addition, inorganic nitrate evaporated in the PAM reactor as sulfate was added to the particles. These results suggest that the chemical composition of aerosols and their degree of photochemical aging, particularly for organics, are also crucial in determining aerosol mass concentrations.
机译:大气气溶胶颗粒具有严重的健康风险,尤其是在东亚这样的地区。我们使用潜在气溶胶质量?(PAM)反应器在2011年8月4日至12日于黄海的Baengnyeong岛调查了环境气溶胶的光化学老化。每隔6分钟从环境空气中或通过潜在的气溶胶质量(PAM)反应器的高氧化环境交替测量气溶胶颗粒的尺寸分布和化学组成。粒度和化学组成是通过结合使用扫描迁移率粒度仪(SMPS)和高分辨率飞行时间气溶胶质谱仪(HR-ToF-AMS)来测量的。在PAM反应器内部,O 3 和OH含量相当于典型大气条件下OH累积暴露量的4.6天。根据化学成分和老化程度将空气分为两种类型:从中国输送的空气,其老化程度更高,具有较高的硫酸盐浓度和O:C比,以及从朝鲜半岛输送的空气,其中与硫酸盐相比,有机物更多,有机碳比率更低,其老化程度更低。对于这两种情况,通过PAM反应器采样时,颗粒硫酸盐质量浓度在200–400?nm的范围内增加。通过PAM反应器取样的有机物占优势的事件,有机物的减少是造成100-200?nm颗粒质量浓度损失的原因。这种损失对m ∕ z?43组分尤为明显,它代表了较少的氧化有机物。代表进一步氧化的有机物的m ∕ z?44组分随着两个事件的向更大尺寸的转移而增加。由于仅使用一次4.6?天的OH暴露,因此无法量化任一事件的最大可能有机物浓度,但是很明显,SO 2 是东北次要气溶胶的主要前体亚洲,尤其是从中国进行远距离运输时。另外,将在PAM反应器中作为硫酸盐蒸发的无机硝酸盐添加到颗粒中。这些结果表明,气溶胶的化学组成及其光化学老化程度,特别是对于有机物,在确定气溶胶质量浓度方面也至关重要。

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