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Secondary inorganic aerosols formation during haze episodes at an urban site in Beijing, China

机译:中国北京某城市霾天气中二次无机气溶胶的形成

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摘要

Severe PM2.5 pollution was observed frequently in Beijing. We conducted highly time-resolved measurements of inorganic ions associated with PM2.5 at an urban site in Beijing from 10 February to 19 March, 2015. The average PM2.5 mass concentrations during the six haze episodes ranged from 113.0 mu g/m(3) to 182.6 mu g/m(3), which were more than 8 times higher than those observed in clean periods. The secondary inorganic species (NH4(+), SO42- and NO3-) in PM2.5 sharply increased during the haze episodes, indicating more extensive formation of SO42- and NO3-. The sulfur oxidation ratios (SOR) and the nitrogen oxidation ratios (NOR) in haze episodes were higher than those in clean periods, which indicated that secondary transformation in haze episodes was more significant than those in clean periods. No correlations between SOR and the oxidants (O-3 and HONO) and the temperature were found, whereas a high correlation between SOR and relative humidity (RH) was found in haze episodes, which implied that sulfate was mainly produced by the aqueous-phase oxidation of SO2 rather than the gas-phase conversion of SO2 to sulfate. The conversion of SO2 to SO42- was observed to be sensitive to changes in RH. Furthermore, the SOR sharply increased at RH 60% with the highest value of 0.88?at RH around 80% during complicated pollution. NO2 played an important role in the rapid sulfate formation with high RH and NH3 neutralization conditions in haze episodes in Beijing. The impact of RH was less apparent for nitrate than for sulfate. Nitrate was found to be produced mainly by photochemical and heterogeneous reactions, while heterogeneous reactions had a greater influence on NOR at nighttime. The NO3-/SO42- ratio indicated that mobile sources contributed more to the formation of PM2.5 than stationary sources. The result suggested the need for control of vehicle emissions to reduce the high levels of NOx and nitrate and the severe PM2.5 pollution in Beijing.
机译:北京经常出现严重的PM2.5污染。我们于2015年2月10日至3月19日在北京市区进行了高度时间分辨的与PM2.5相关的无机离子测量。在6次霾天气中,PM2.5的平均质量浓度为113.0μg / m( 3)至182.6μg / m(3),比清洁时期的观测值高8倍以上。在雾霾发作期间,PM2.5中的次生无机物(NH4(+),SO42-和NO3-)急剧增加,表明SO42-和NO3-的形成更加广泛。霾事件中的硫氧化比(SOR)和氮氧化率(NOR)高于清洁时期的烟氧化,表明霾事件中的二次转化要比清洁时期的显着。没有发现SOR与氧化剂(O-3和HONO)和温度之间的相关性,而在霾天气中,SOR与相对湿度(RH)之间的相关性很高,这表明硫酸盐主要由水相产生氧化SO2而不是将SO2气相转化为硫酸盐。观察到SO2向SO42-的转化对RH的变化很敏感。此外,在复杂污染期间,相对湿度在RH> 60%时急剧增加,在RH的80%左右最高值为0.88?。在北京霾天气中,NO2在高RH和NH3中和条件下快速形成硫酸盐中起着重要作用。相对于硫酸盐,RH对硝酸盐的影响不那么明显。硝酸盐主要通过光化学反应和异相反应产生,而异质反应在夜间对NOR的影响更大。 NO3- / SO42-比值表明,移动源比固定源对PM2.5形成的贡献更大。结果表明,有必要控制车辆的排放量,以减少北京的高水平NOx和硝酸盐以及严重的PM2.5污染。

著录项

  • 来源
    《Atmospheric environment》 |2018年第3期|275-282|共8页
  • 作者单位

    Municipal Res Inst Environm Protect, Natl Engn Res Ctr Urban Environm Pollut Comrol, Beijing 100037, Peoples R China;

    Municipal Res Inst Environm Protect, Natl Engn Res Ctr Urban Environm Pollut Comrol, Beijing 100037, Peoples R China;

    Municipal Res Inst Environm Protect, Natl Engn Res Ctr Urban Environm Pollut Comrol, Beijing 100037, Peoples R China;

    Municipal Res Inst Environm Protect, Natl Engn Res Ctr Urban Environm Pollut Comrol, Beijing 100037, Peoples R China;

    Municipal Res Inst Environm Protect, Natl Engn Res Ctr Urban Environm Pollut Comrol, Beijing 100037, Peoples R China;

    Municipal Res Inst Environm Protect, Natl Engn Res Ctr Urban Environm Pollut Comrol, Beijing 100037, Peoples R China;

    Municipal Res Inst Environm Protect, Natl Engn Res Ctr Urban Environm Pollut Comrol, Beijing 100037, Peoples R China;

    Municipal Res Inst Environm Protect, Natl Engn Res Ctr Urban Environm Pollut Comrol, Beijing 100037, 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; PM2.5; Sulfate; Nitrate; Secondary formation;

    机译:雾度;PM2.5;硫酸盐;硝酸盐;二次形成;

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