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Evaluating the degree of oxygenation of organic aerosol during foggy and hazy days in Hong Kong using high-resolution time-of-flight aerosol mass spectrometry (HR-ToF-AMS)

机译:使用高分辨率飞行时间气溶胶质谱法(HR-TOF-AMS)在香港雾化和朦胧日内有机气溶胶氧合程度评价

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The chemical characteristics of organic aerosol (OA) are still poorly constrained. Here we present observation results of the degree of oxygenation of OA based on high-resolution time-of-flight aerosol mass spectrometry (HR-ToF-AMS) measurements made at a coastal site in Hong Kong from late April to the end of May in 2011. Two foggy periods and one hazy period were chosen for detailed analysis to compare the changes in the degree of oxygenation of OA due to different processes. Using HR-ToF-AMS measured inorganic species as input, the Extended Aerosol Inorganic Model (E-AIM) predicted a fine-particle liquid water content (LWCfp) up to 85 μg m?3 during the foggy days. Particle concentration as measured by HR-ToF-AMS was up to 60 μg m?3 during the hazy days and up to 30 μg m?3 during the foggy days. The degree of oxygenation of OA, as indicated by several parameters including the fraction of m/z 44 in organic mass spectra (f44), the elemental ratio of oxygen to carbon (O : C), and the carbon oxidation state (OSc), was evaluated against the odd oxygen (Ox) concentration, LWCfp, ionic strength (IS), and in situ pH (pHis). Observations suggest that the high concentration of OA (on average 11 μg m3) and the high degree of oxygenation (f44 = 0.15, O : C = 0.51, and OSc = ?0.31) during the hazy period were mainly due to gas-phase oxidation. During the foggy periods with low photochemical activities, the degree of oxygenation of OA was almost as high as that on the hazy days, and significantly higher than that during non-foggy/non-hazy days. However, the OA evolved quite differently in the two foggy periods. The first foggy period in late April saw a larger LWCfp and a lower Ox concentration and the OA were made up of ~ 20 % semi-volatile oxygenated organic aerosol (SVOOA) as resolved by positive matrix factorization (PMF). In the second foggy period in mid-May, higher Ox concentration and lower LWCfp were observed, and the OA were found to contain 50 % low-volatility oxygenated organic aerosols (LVOOA). An examination of the particle characteristics (pHis, IS, and LWCfp) suggests that partitioning may have been the dominating process through which oxygenated species were incorporated into the particle phase during the first foggy period, while oxidation in the aqueous phase dominated over gas-phase processes during the second foggy period.
机译:有机气溶胶(OA)的化学特征仍然受到严重。在这里,我们基于在4月下旬到5月底,在香港沿海地区的高分辨率飞行时间氧气质谱(HR-TOF-AMS)测量来呈现OA氧化程度的观察结果选择两个有雾的时期和一个朦胧的时间,以进行详细分析,以比较由于不同的过程,比较OA的氧气程度的变化。使用HR-TOF-AMS测量的无机物质作为输入,延伸的气溶胶无机模型(E-AIM)在雾化天期间预测了高达85μgm≤3的细颗粒液体水含量(LWCFP)。通过HR-TOF-AMS测量的颗粒浓度在朦胧的日子期间高达60μgm≤3,在雾化天期间高达30μgm≤3。 OA的氧合度,如有机质谱(F44)中的M / Z 44分数的若干参数,氧与碳(O:C)的元素比和碳氧化状态(OSC),对奇氧(OX)浓度,LWCFP,离子强度(IS)和原位pH(PHI)评估。观察结果表明,在朦胧时期期间,高浓度的OA(平均11μgm3)和高氧合(F44 = 0.15,O:c = 0.51和OSC = 0.31)主要是由于气相氧化。在光化学活动低的雾期间,OA的氧气程度几乎高于朦胧的日子,并且显着高于非雾/非朦胧日期。然而,OA在两个有雾的时期中进化得非常不同。 4月下旬的第一个有雾期看到较大的LWCFP和较低的牛浓度,并且OA由〜20%的半挥发性含氧有机气溶胶(SVOOA)组成,如阳性基质分子(PMF)分解。在5月中旬的第二雾时段中,观察到更高的牛浓度和更低的LWCFP,发现OA含有> 50%低挥发性的含氧有机气溶胶(LVOOA)。对颗粒特征(PHI,LWCFP)的检查表明,分区可能是在第一有雾周期内掺入颗粒相中的氧化物质中的主导过程,而水相中的氧化在占气相中的氧化第二雾期间的过程。

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