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Significant Increase of Aromatics-Derived Secondary Organic Aerosol during Fall to Winter in China

机译:秋季至冬季,源自芳香族的次生有机气溶胶显着增加

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摘要

Human activities release large amounts of anthropogenic pollutants into the air, and thereby produce substantial secondary organic aerosol (SOA). Aromatic hydrocarbons (AHs) that mainly emitted from coal combustion, transportation, solvent use and biofuel/biomass burning, are a major class of anthropogenic SOA precursors. At present, there are few field studies focusing on AH-derived SOA (SOA_A) on a continental scale, especially in polluted regions of the world. In this study, a one-year concurrent observation of the SOA_A tracer, 2,3-dihydroxy-4-oxopentanoic acid (C_5H_8O_5, DHOPA) was carried out at 12 sites across six regions of China for the first time. The annual averages of DHOPA among the 12 sites ranged from 1.23 to 8.83 ng m~(-3) with a mean of 3.48 ± 1.96 ng m~(-3). At all observation sites, the concentrations of DHOPA from fall to spring were significantly higher than those in summertime, and positive correlations were observed between DHOPA and the biomass burning tracer (levoglucosan). This indicated that such a nationwide increase of SOA_A during the cold period was highly associated with the enhancement of biomass burning emission. In the northern China, the highest levels of DHOPA were observed in the coldest months during winter, probably due to the enhancement of biofuel and coal consumption for household heating. In the southern China, the highest levels of DHOPA were mostly observed in fall and spring, which were associated with the enhancement of open biomass burning. The apparent increases of DHOPA and levoglucosan levels during the cold period and the negative correlations of visibility with DHOPA and levoglucosan imply that the reduction of SOA_A amount and biomass burning emission is an efficient way to reduce haze pollution during fall to winter in China.
机译:人类活动将大量人为污染物释放到空气中,从而产生大量的二次有机气溶胶(SOA)。主要从煤炭燃烧,运输,溶剂使用和生物燃料/生物质燃烧产生的芳香烃(AHs)是人为SOA的主要前体。目前,在大陆范围内,尤其是在世界污染地区,很少有针对AH来源的SOA(SOA_A)的现场研究。在这项研究中,首次在中国六个地区的12个地点进行了为期一年的同时观测SOA_A示踪剂2,3-二羟基-4-氧戊酸(C_5H_8O_5,DHOPA)。 12个站点中DHOPA的年平均值介于1.23至8.83 ng m〜(-3)之间,平均值为3.48±1.96 ng m〜(-3)。在所有观察点,从秋季到春季,DHOPA的浓度均显着高于夏季,并且DHOPA与生物质燃烧示踪剂(左旋葡聚糖)之间存在正相关。这表明在寒冷时期,全国范围内SOA_A的增加与生物质燃烧排放的增加高度相关。在中国北方,在冬季最冷的月份观测到DHOPA的最高水平,这可能是由于生物燃料和家庭取暖用煤的消耗增加了。在中国南部,DHOPA的最高水平主要发生在秋季和春季,这与露天生物质燃烧的增强有关。在寒冷时期,DHOPA和左旋葡聚糖的含量明显增加,并且与DHOPA和左旋葡聚糖的能见度呈负相关关系,这表明减少SOA_A量和减少生物质燃烧排放是减少秋冬季雾霾污染的有效方法。

著录项

  • 来源
    《Environmental Science & Technology》 |2017年第13期|7432-7441|共10页
  • 作者单位

    State Key Laboratory of Organic Geochemistry and Guangdong Provincial Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China;

    State Key Laboratory of Organic Geochemistry and Guangdong Provincial Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China,University of Chinese Academy of Sciences, Beijing 100049, China;

    State Key Laboratory of Organic Geochemistry and Guangdong Provincial Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China;

    State Key Laboratory of Organic Geochemistry and Guangdong Provincial Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China,University of Chinese Academy of Sciences, Beijing 100049, China;

    State Key Laboratory of Organic Geochemistry and Guangdong Provincial Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China,University of Chinese Academy of Sciences, Beijing 100049, China;

    State Key Laboratory of Organic Geochemistry and Guangdong Provincial Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China;

    State Key Laboratory of Organic Geochemistry and Guangdong Provincial Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China;

    State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, China,Center for Excellence in Regional Atmospheric Environment, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021, China;

    State Key Laboratory of Organic Geochemistry and Guangdong Provincial Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China,Center for Excellence in Regional Atmospheric Environment, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021, China;

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  • 正文语种 eng
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