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Deciphering the Role of Radical Precursors during the Second Texas Air Quality Study

机译:在第二次德克萨斯州空气质量研究中阐明自由基前体的作用

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摘要

The Texas Environmental Research Consortium (TERC) funded significant components of the Second Texas Air Quality Study (TexAQS II), including the TexAQS IIrnRadical and Aerosol Measurement Project (TRAMP) and instrumented flights by a Piper Aztec aircraft. These experiments called attention to the role of short-lived radical sources such as formaldehyde (HCHO) and nitrous acid (HONO) in increasing ozone productivity. TRAMP instruments recorded daytime HCHO pulses as large as 32 parts per billion (ppb) originating from upwind industrial activities in the Houston Ship Channel, where in situ surface monitors detected HCHO peaks as large as 52 ppb. Moreover, Ship Channel petrochemical flares were observed to produce plumes of apparent primary HCHO. In one such combustion plume that was depleted of ozone by large emissions of oxides of nitrogen (NO_x), the Piper Aztec measured a ratio of HCHO to carbon monoxide (CO) 3 times that of mobile sources. HCHO from uncounted primary sources or ozonolysis of underestimated olefin emissions could significantly increase ozone productivity in Houston beyond previous expectations. Simulations with the CAMx model show that additional emissions of HCHO from industrial flares or mobile sources can increase peak ozone in Houston by up to 30 ppb. Other findings from TexAQS II include significant concentrations of HONO throughout the day, well in excess of current air quality model predictions, with large nocturnal vertical gradients indicating a surface or near-surface source of HONO, and large concentrations of nighttime radicals (~30 parts per trillion [ppt] HO_2). HONO may be formed heterogeneously on urban canopy or particulate matter surfaces and may be enhanced by organic aerosol of industrial or motor vehicular origin, such as through conversion of nitric acid (HNO_3). Additional HONO sources may increase daytime ozone by more than 10 ppb. Improving the representation of primary and secondary HCHO and HONO in air quality models could enhance the simulated effectiveness of control strategies.
机译:德克萨斯州环境研究协会(TERC)资助了第二次德克萨斯州空气质量研究(TexAQS II)的重要组成部分,其中包括TexAQS IIn辐射和气溶胶测量项目(TRAMP)以及Piper Aztec飞机进行的仪表飞行。这些实验引起人们对诸如甲醛(HCHO)和亚硝酸(HONO)等短寿命自由基源在提高臭氧生产率中的作用的关注。 TRAMP仪器记录的白天HCHO脉冲高达十亿分之32(ppb),源于休斯敦船舶航道的逆风工业活动,该现场现场监测仪检测到HCHO峰值高达52 ppb。此外,观察到船道石化火炬产生明显的初级HCHO羽。在一种这样的燃烧羽流中,由于大量氮氧化物(NO_x)的排放而耗尽了臭氧,Piper Aztec测量出HCHO与一氧化碳(CO)的比率是移动源的3倍。来源不明的HCHO或低估烯烃排放的臭氧分解可能大大增加休斯顿的臭氧生产率,超出先前的预期。 CAMx模型的模拟表明,工业火炬或移动源产生的HCHO额外排放量可使休斯顿的臭氧峰值增加30 ppb。 TexAQS II的其他发现包括:全天浓度很高的HONO,远远超出了当前的空气质量模型预测,夜间垂直梯度较大表明HONO的表面或近表面来源,夜间自由基的浓度较高(约30个份每兆[ppt] HO_2)。 HONO可以在城市冠层或颗粒物表面上异质地形成,并且可以通过工业或机动车辆来源的有机气溶胶来增强,例如通过硝酸(HNO_3)的转化。其他HONO源可能会使白天的臭氧增加10 ppb以上。改善空气质量模型中主要和次要HCHO和HONO的表示,可以提高控制策略的模拟效果。

著录项

  • 来源
    《Journal of the air & waste management association》 |2009年第11期|1258-1277|共20页
  • 作者单位

    Houston Advanced Research Center, The Woodlands, TX Texas Environmental Research Consortium, Houston, TX;

    Department of Atmospheric Chemistry, University of Houston, Houston, TX;

    Department of Atmospheric Chemistry, University of Houston, Houston, TX;

    Department of Atmospheric and Oceanic Sciences, University of California-Los Angeles, Los Angeles, CA;

    Department of Tropospheric Chemistry, University of New Hampshire, Durham, NH;

    Department of Civil and Environmental Engineering, Rice University, Houston, TX;

    Department of Meteorology, Pennsylvania State University, University Park, PA;

    Institute for Air Science, Baylor University, Waco, TX;

    Air Quality Design, Inc., Golden, CO;

    Department of Atmospheric and Aquatic Sciences, University of North Carolina-Chapel Hill, Chapel Hill, NC;

    Department of Atmospheric and Aquatic Sciences, University of North Carolina-Chapel Hill, Chapel Hill, NC;

    U.S. Environmental Protection Agency, National Center for Environmental Assessment, Research Triangle Park, NC;

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