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Chemical characteristics of submicron aerosol particles during a long-lasting haze episode in Xiamen, China

机译:厦门长期霾天气中亚微米气溶胶颗粒的化学特征

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摘要

A long-lasting haze episode has been first observed with a mean atmospheric visibility of 8.6 km since last decades over Xiamen. An Aerodyne Aerosol Mass Spectrometer (AMS) was deployed to obtain the size-resolved chemical composition of non-refractory submicron particles (NR-PM1) at 10 min resolution. Characteristics of aerosol particles in haze days have been analyzed and compared to in clear days and rainy days. The mean concentration of PM2.5 was about 213.3 mu g m(-3) (+/- 16.9 mu g m(-3)) during haze days, which was about 4 times higher than during clear days. Organics, sulfate and ammonium were the major components in these supper fine particles, accounting for 37.2% (+/- 0.11), 28.7% (+/- 0.11) and 12.0% (+/- 0.11), respectively, during haze days. The size distributions of aerosol species were characterized by a major accumulation mode peaking at a vacuum aerodynamic diameter of 390 nm during clear days, 427 nm during rainy days and 579 rim during haze days. High concentrations of SO42-, NO3- and NH4+ were observed and the average values of sulfur oxidation ratios (SOR) and nitrogen oxidation ratios(NOR) were up to 0.56 (+/- 0.17) and 0.25 (+/- 0.11) during haze days. Positive Matrix Factorization (PMF) was used to identity a hydrocarbon-like organic aerosol (HOA) and an oxygenated organic aerosol (OOA) component. It showed that OOA components were probably representative of SOA in Xiamen. The average value of NO3-/SO42- was 0.28 during clear days, 0.20 during rainy days and 0.59 during haze days, indicating that pollutants from local vehicle exhaust sources were accumulated in haze days. During haze days, the main air mass (accounted for 81%) transported from the northeast of China, implying that the haze pollution was partly influenced by the pollutants transported from heavy haze areas in China. Pollution accumulated by local processes, secondary aerosol formation and the stagnation meteorological atmosphere dominated the formation of the haze event. (C) 2015 Elsevier Ltd. All rights reserved.
机译:自过去几十年来,厦门地区首次观测到长期霾霾,平均大气能见度为8.6 km。部署了Aerodyne气溶胶质谱仪(AMS),以10分钟的分辨率获得了尺寸分辨的非难熔亚微米颗粒(NR-PM1)的化学成分。分析和比较了阴霾天和阴雨天的气溶胶颗粒特征。在阴霾天,PM2.5的平均浓度约为213.3μg m(-3)(+/- 16.9μg m(-3)),比晴天高约4倍。这些超细颗粒中的主要成分是有机物,硫酸盐和铵,在雾霾天中分别占37.2%(+/- 0.11),28.7%(+/- 0.11)和12.0%(+/- 0.11)。气溶胶种类的大小分布的特征是主要的积聚模式,在晴天,真空空气动力学直径为390 nm,在雨天为427 nm,在雾霾天为579边缘,达到峰值。在雾霾中观察到高浓度的SO42-,NO3-和NH4 +,硫氧化比(SOR)和氮氧化比(NOR)的平均值分别高达0.56(+/- 0.17)和0.25(+/- 0.11)天。正矩阵分解(PMF)用于鉴定类烃类有机气溶胶(HOA)和氧化有机气溶胶(OOA)组分。结果表明,OOA组件可能是厦门SOA的代表。 NO3- / SO42-的平均值在晴天时为0.28,在雨天时为0.20,在霾天时为0.59,表明来自本地汽车尾气源的污染物在霾天时累积。在霾天期间,主要的空气质量(占81%)从中国的东北部转移出去,这意味着霾污染受到了中国重霾地区排放的污染物的部分影响。局部过程累积的污染,二次气溶胶的形成和停滞的气象气氛主导了霾事件的形成。 (C)2015 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Atmospheric environment》 |2015年第7期|118-126|共9页
  • 作者单位

    Third Inst Oceanog, SOA, Key Lab Global Change & Marine Atmospher Chem, Xiamen, PR, Peoples R China;

    Third Inst Oceanog, SOA, Key Lab Global Change & Marine Atmospher Chem, Xiamen, PR, Peoples R China;

    Third Inst Oceanog, SOA, Key Lab Global Change & Marine Atmospher Chem, Xiamen, PR, Peoples R China;

    Third Inst Oceanog, SOA, Key Lab Global Change & Marine Atmospher Chem, Xiamen, PR, Peoples R China;

    Third Inst Oceanog, SOA, Key Lab Global Change & Marine Atmospher Chem, Xiamen, PR, Peoples R China;

    Third Inst Oceanog, SOA, Key Lab Global Change & Marine Atmospher Chem, Xiamen, PR, Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Haze; Aerosol particles; Size distribution; PM1; Chemical composition; Air pollution;

    机译:雾度;气溶胶颗粒;粒度分布;PM1;化学成分;空气污染;

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