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首页> 外文期刊>Journal of the air & waste management association >Projected ozone trends and changes in the ozone-precursor relationship in the South Coast Air Basin in response to varying reductions of precursor emissions
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Projected ozone trends and changes in the ozone-precursor relationship in the South Coast Air Basin in response to varying reductions of precursor emissions

机译:响应于前体排放量的不同减少,预计的臭氧趋势以及南海岸空气盆地中臭氧与前体关系的变化

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摘要

This study examined the effects of varying future reductions in emissions of oxides of nitrogen (NO_x) and volatile organic compounds (VOC) on the location and magnitude of peak ozone levels within California's South Coast Air Basin (SoCAB or Basin). As ozone formation is currently VOC-limited in the Basin, model simulations with 2030 baseline emissions (-61% for NO_x and -32% for VOC from 2008) predict 10-20% higher peak ozone levels (i.e., NO_x disbenefit) in the western and central SoCAB compared with the 2008 base simulation. With additional NO_x reductions of 50% beyond the 2030 baseline emissions (-81% from 2008), the predicted ozone levels are reduced by about 15% in the eastern SoCAB but remain comparabie to 2008 levels in the western and central Basin. The Basin maximum ozone site shifts westward to more populated areas of the Basin and will result potentially in greater population-weighted exposure to ozone with even a relatively small shortfall in the required NO_x reductions unless accompanied by additional VOC reductions beyond 2030 baseline levels. Once committed to a NO_x-focused control strategy, NO_x reductions exceeding 90% from 2008 levels will be necessary to attain the ozone National Ambient Air Quality Standards (NAAQS). The findings from this study and other recent work that the current VOC emission estimates are underestimated by about 50% suggest that greater future VOC reductions will be necessary to reach the projected 2030 baseline emissions. Increasing the base year VOC emissions by a factor of 15 result in higher 2008 baseline ozone predictions, lower relative response factors, and about 20% lower projected design values. If correct, these findings have important implications for the total and optimum mix of VOC and NO_x emission reductions that will be required to attain the ozone NAAQS in the SoCAB. Implications: Results of this study indicate that ozone levels in the western and central SoCAB would remain the same or increase with even a relatively small shortfall in the projected NO_x reductions under planned NO_x-focused controls. This possibility, therefore, warrants a rigorous analysis of the costs and effects of varying reductions of VOC and NO_x on the formation and combined health impacts of ozone and secondary particles. Given the nonlinearity of ozone formation, such analyses should include the implications of gradually increasing global background ozone concentrations and the Basin's topography and meteorology on the practical limits of alternative emission control strategies.
机译:这项研究检查了未来氮氧化物(NO_x)和挥发性有机化合物(VOC)排放量的不同减少对加利福尼亚州南海岸空气盆地(SoCAB或盆地)内臭氧峰值水平的位置和大小的影响。由于该盆地目前的臭氧形成受到VOC的限制,因此,以2030年基准排放量(从2008年开始,NO_x为-61%,VOC为-32%)进行的模型模拟预测,该地区的峰值臭氧水平(即NO_x不利)将增加10-20%。西部和中部SoCAB与2008年的基础仿真相比。到2030年基准排放量增加50%的NO_x排放量(比2008年减少-81%)后,东部SoCAB的预测臭氧水平降低了约15%,但与西部和中部盆地的2008年水平保持了可比性。流域最大的臭氧位置向西转移到流域人口较多的地区,除非与2030年基准水平相比有更多的VOC降低,否则可能导致更大的人口加权臭氧暴露,甚至所需的NO_x减排量相对较小的缺口。一旦致力于以NO_x为重点的控制策略,则要达到臭氧国家环境空气质量标准(NAAQS),必须将NO_x的排放量比2008年的水平降低90%以上。这项研究和其他近期工作得出的结论是,当前的VOC排放估算值被低估了约50%,这表明,为达到预计的2030年基准排放量,有必要进一步降低VOC的排放量。将基准年的VOC排放量增加15倍,会导致2008年基准臭氧预测值更高,相对响应因子更低,并且预计设计值降低约20%。如果正确,这些发现对实现SoCAB中的臭氧NAAQS所需的VOC和NO_x减排总量的最佳组合具有重要意义。启示:这项研究的结果表明,在以NO_x为重点的控制措施下,预计的NO_x减少量相对较小的缺口,西部和中部SoCAB中的臭氧水平将保持不变或增加。因此,这种可能性需要对VOC和NO_x的不同减少量对臭氧和二次颗粒的形成以及对健康的综合影响的成本和影响进行严格分析。考虑到臭氧形成的非线性,此类分析应包括逐步增加全球本底臭氧浓度以及流域的地形和气象对替代排放控制策略的实际限制的影响。

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    Division of Atmospheric Sciences, Desert Research Institute, Nevada System of Higher Education, 2215 Raggio Parkway, Reno, NV 89512, USA;

    Division of Atmospheric Sciences, Desert Research Institute, Nevada System of Higher Education, Reno, NV, USA;

    Department of Chemistry, Howard University, Washington, DC, USA;

    Department of Chemistry, Howard University, Washington, DC, USA;

    Department of Physics, University of Texas El Paso, El Paso, TX, USA;

    Department of Physics, University of Texas El Paso, El Paso, TX, USA;

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