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Characterization of nighttime formation of particulate organic nitrates based on high-resolution aerosol mass spectrometry in an urban atmosphere in China

机译:基于高分辨率气溶胶质谱法在中国城市大气中夜间形成颗粒状有机硝酸盐的表征

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Organic nitrates are important atmospheric species that significantly affect the cycling of NOsubx/sub and ozone production. However, characterization of particulate organic nitrates and their sources in polluted atmosphere is a big challenge and has not been comprehensively studied in Asia. In this study, an aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) was deployed at an urban site in China from 2015 to 2016 to characterize particulate organic nitrates in total nitrates with a high time resolution. Based on the cross-validation of two different data processing methods, organic nitrates were effectively quantified to contribute a notable fraction of organic aerosol (OA), namely 9?%–21?% in spring, 11?%–25?% in summer, and 9?%–20?% in autumn, while contributing a very small fraction in winter. The good correlation between organic nitrates and fresh secondary organic aerosol (SOA) at night, as well as the diurnal trend of size distribution of organic nitrates, indicated a key role of nighttime local secondary formation of organic nitrates. Furthermore, theoretical calculations of nighttime SOA production of NOsub3/sub reactions with volatile organic compounds (VOCs) measured during the spring campaign were performed, resulting in three biogenic VOCs ( α -pinene, limonene, and camphene) and one anthropogenic VOC (styrene) identified as the possible key VOC precursors to particulate organic nitrates. The comparison with similar studies in the literature implied that nighttime particulate organic nitrate formation is highly relevant to NOsubx/sub levels. This study proposes that unlike the documented cases in the United States and Europe, modeling nighttime particulate organic nitrate formation in China should incorporate not only biogenic VOCs but also anthropogenic VOCs for urban air pollution, which needs the support of relevant smog chamber studies in the future.
机译:有机硝酸盐是重要的大气物质,会显着影响NO x 的循环和臭氧的产生。然而,在大气中表征颗粒状有机硝酸盐及其来源是一个巨大的挑战,在亚洲尚未进行全面研究。在这项研究中,从2015年到2016年,在中国的城市地区部署了Aerodyne高分辨率飞行时间气溶胶质谱仪(HR-ToF-AMS),以高时间分辨率表征了总硝酸盐中的颗粒有机硝酸盐。基于两种不同数据处理方法的交叉验证,有机硝酸盐得到了有效定量,以贡献显着比例的有机气溶胶(OA),即春季为9 %% – 21%,夏季为11 %% – 25%。 ,秋季为9 %% – 20 %%,而冬季的贡献很小。夜间有机硝酸盐与新鲜的次要有机气溶胶(SOA)之间的良好相关性以及有机硝酸盐的尺寸分布的日变化趋势,表明夜间有机硝酸盐局部次生形成的关键作用。此外,进行了春季运动期间测量的夜间SOA产生的NO 3 反应与挥发性有机化合物(VOC)的理论计算,得出了三种生物源VOC(α-pine烯,li烯和樟脑)。一种人为的挥发性有机化合物(苯乙烯)被确定为有机硝酸盐颗粒的重要挥发性有机化合物前体。与文献中类似研究的比较表明,夜间颗粒有机硝酸盐的形成与NO x 水平高度相关。这项研究提出,与美国和欧洲有记录的案例不同,对中国夜间有机硝酸盐形成的建模不仅应包括生物VOC,而且还应包括人为VOC以解决城市空气污染,这在未来需要相关雾气室研究的支持。 。

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