共查询到19条相似文献，搜索用时 171 毫秒
1.
应用查表法模拟区域对流层O3、Nox分布和演化的研究 总被引：1，自引：0，他引：1
应用STEM-II气相光化学模式探讨了影响对流层O3、NOx气相光化学转化率的各物理、化学因子。表明在我国多数地区光化学污染物特征(NMHC/NOx较高)下，光辐射强度、温度、初始O3浓度和NOx浓度是影响O3、NOx气相光化学转化率的主要因子。将以上因子分档组合，计算并建立了各种情况下O3、NOx气相光化学转化率的查算表，并将之用于模拟区域O3、NOx的演化和分布。结果表明，与光化学模式直接耦合计算法相比，该方法既能显著缩短计算时间，又能基本反映大气化学反应的非线性过程，并与直接耦合法符合得较好。 相似文献
2.
应用大气光化学模式研究了日间影响NOx光化学转化率的主要物理化学因子.探讨了在不同NMHC/NOx比值时,NOx光化学特征及其转化产物的变化规律.结果表明,影响NOx转化率的主要因子是阳光辐射强度和NMHC/NOx比值.但在NMHC/NOx比值很低时,光强的增加并不能显著提高NOx转化率.温度和初始臭氧浓度对NOx转化率的影响次之.相对湿度对NOx转化率的影响较小.在不同NMHC/NOx比值下,NOx转化特征和产物有很大区别.NMHC/NOx比值高时,产物中PAN＞HNO3.NMHC/NOx比值中(低)时,产物主要是HNO3,PAN等有机氮不到10%(1%).最后初步比较了模拟和观测的NOy组成. 相似文献
3.
地面臭氧的变化规律和计算方法的初步研究Ⅰ.紫外波段 总被引：5，自引：1，他引：4
通过对广州鼎湖山近地面O3、NOx、太阳辐射、气象参数等项目的观测和理论分析,研究了地面O3与NOx等微量气体及太阳辐射的变化规律,详细讨论了紫外波段、不同天气条件地面O3与NOx,光化学反应、气溶胶、光化辐射等之间复杂的关系.用光能量传输与守恒的观点来考虑大气中与紫外辐射有关的主要过程,并以此来研究大气光化学过程中所遵循的能量规律,建立了一个简单、实用、省时的统计模式,用于计算地面O3浓度.结果表明,不同情况下计算值与观测值均吻合较好. 相似文献
4.
地面臭氧的变化规律和计算方法的初步研究Ⅱ.可见光波段 总被引：7，自引：0，他引：7
通过对广州鼎湖山近地面O3、NOx、太阳辐射,气象参数等项目的观测和理论分析,研究了地面O3与NOx等微量气体及太阳可见光辐射的变化规律,详细讨论了可见光波段、不同天气条件地面O3与NOx、光化学反应、气溶胶、可见光辐射等之间复杂的关系.提出以光能量传输与守恒的观点来考虑大气中与可见光辐射有关的主要过程,并以此来研究大气光化学过程中所遵循的能量规律,建立了一个简单、实用、省时的统计模式,用于计算地面O3浓度.结果表明:不同情况下,计算值与观测值吻合得均比较一致. 相似文献
5.
光化学烟雾的控制试验 总被引：2，自引：0，他引：2
利用MM5与RADM的耦合模式,设计了3个削减源排放的试验,用以探讨控制光化学污染的有效途径。试验结果表明,在NMHC/NOx比值很大的前提条件下,NOx地面源排放的削减对降低大气中O3含量的作用最显著,而削减NMHC对降低大气中PAN含量的作用明显,同时削减NMHC和NOx是降低大气光化学污染强度的最佳途径。 相似文献
6.
近地面O3变化化学反应机理的数值研究 总被引：34，自引：1，他引：33
利用中尺度气象模式（MM5）及区域化学模式（RADM）对中国地区近地面O3变化化学反应机理进行了数值模拟研究。主要研究了近地面O3变化与其主要前体物NMHC（非甲烷烃）、NOx、CO等之间复杂相互作用关系。主要结论为:（1） 污染地区近地面O3变化主要受光化学作用控制;而清洁地区地面O3变化主要受大气背景O3浓度影响。（2）NMHC和NOx的变化对HO2和OH自由基的影响是十分复杂的,O3的反馈作用对自由基的影响是不可忽视的。（3）在高NOx污染地区的地面上空可能出现高O3污染。（4）在O3光化学反应机理中同样存在线性相关关系。 相似文献
7.
将广泛应用于东亚地区的LLA(Lurmann Lloyd Atkinson)化学机制耦合到欧拉型区域空气质量模式(RAQM),并考虑区域污染物长期模拟研究中降水随时间变化的非均匀性,讨论了湍流参数化过程中相似理论在近地层和全边界层的应用对湍流垂直扩散系数(Kz)与干沉降速度(V),O3与NOx浓度的影响。结果表明,全边界层应用相似理论明显低估了Kz值,近地层50m处Kz值被低估20%以上,750m处其值被低估约70%;O3、NOx的干沉降速度在日本东部与南部海域被低估了10%以上,在朝鲜半岛东部和西部海域模拟值普遍偏高。Kz和干沉降速度的不同直接影响污染物的浓度和沉降量分布。Kz值的被低估对NOx浓度有明显影响,在近地层50m处NOx浓度最大可增加约30%,整个边界层中NOx平均浓度除台湾省东北海域外普遍增加5%~20%。O3浓度则受干沉降作用的影响较大。虽然近地层、全边界层分别应用相似理论都较好地模拟了O3与NOx峰值浓度出现的时间,但相似理论应用于全边界层会引起较大的误差。即使是大区域、长期空气质量模拟研究,也建议相似理论仅应用于近地层,且模式第一层高度应设置在常通量层内。 相似文献
8.
区域化学输送模式中NO x和O3源示踪法的引入 总被引：4，自引：0，他引：4
发展了化学输送模式中氮氧化合物(NOx)和臭氧(O3)的一种源示踪方法,对这种示踪法及其应用模式作了详细介绍,并结合臭氧光化学反应机理的分析描述了NOx和O3示踪物浓度方程的推导过程。将这种示踪法引用到区域化学输送模式中,并以太原和石家庄地表NOx人为排放产生的活性氮化物和臭氧为例,演示了污染物向北京的输送过程,模拟的O3,NOx和NOz示踪物浓度时空分布与O3,NOx和NOz在大气中的衰减尺度分析一致,表明该示踪法是一种有效的研究区域氮氧化物以及臭氧来源和输送转化过程的方法。个例模拟分析结果显示:太原和石家庄的地表人为排放产生的NOx本身并不能输送到北京,但通过它们产生的O3和HNO3可以输送到北京,对北京地表附近大气污染造成影响。 相似文献
9.
鼎湖山森林地区臭氧及其前体物的变化特征和分析 总被引：18，自引：2，他引：16
通过对鼎湖山森林地区近地面O3和NOx浓度、太阳辐射、气象参数等为期一年的观测和资料分析,给出了地面O3和NOx浓度、太阳辐射的变化规律及其相互之间的关系.地面O3、NOx、CO、SO2浓度以及紫外辐射、太阳总辐射等有明显的日变化和季节变化.不同因子对O3的敏感性试验结果表明,晴天和实际天气,O3浓度对NO、NO2浓度的变化最为敏感,其次是水汽、气溶胶,最后是紫外辐射.所有因子的变化均引起O3在湿季比干季更大的变化率,因此在研究臭氧化学和光化学时,应该考虑水汽以及OH自由基的重要作用.对于晴天和实际天气的逐时值和日平均值而言,O3浓度与NO2/NO之间存在很好的正相关关系,比值NO2/NO可以作为判断O3峰值出现的一个指标.O3极值的出现既受NO和NOx影响,也受气象因素(温湿度、云、风、雾、降雨)和辐射的影响.周末O3、NOx浓度及NO2/NO有规律的增大,表明实验地点的大气受到人为污染源的影响. 相似文献
10.
中国地区臭氧前体物对地面臭氧的影响 总被引：5，自引：1，他引：4
利用GEOS-Chem模式的数值试验结果,研究中国地区NOx和两类VOCs对O3质量浓度分布及其化学机理的影响。研究表明,NOx的减少会使得中国西部O3质量浓度显著降低,但在冬季NOx的减少会使得东北、华北地区O3质量浓度上升。而京津唐地区由于VOCs/NOx比值偏低,不能通过单一减少NOx来控制O3质量浓度。VOCs排放的减少会使得我国东部地区O3质量浓度大幅减少,其中人为VOCs的减少能降低我国东部地面O3质量浓度,而生物VOCs的减少只能在夏秋季有效减少我国东部地区35°N以南区域的地面O3质量浓度。控制地面O3质量浓度时,中国西部主要考虑NOx的减排,东部35°N以北主要考虑AVOCs的减排,而30~35°N应同时考虑AVOCs和BVOCs的减排,在30°N以南的地区,则需要全面考虑NOx和VOCs的减排。 相似文献
11.
12.
主要介绍一个可用于化学输送模式的对流层O3来源和过程追踪技术。该方法可定量估算不同区域的光化学反应通过输送过程对目标地区O3浓度的贡献,并且克服了光化学非线性特征对估算结果的影响。以研究2001年中国南部和北部光化学生成O3的输送为例,通过与改进的敏感性分析方法比较,系统评估了该方法的合理性。比较结果表明,两种方法的估算结果在水平、垂直分布和典型输送个例等方面具有良好的一致性,说明污染物来源和过程追踪技术可以为量化区域输送对目标地区O3浓度的影响提供合理结果。个例模拟分析的结果也表明,中国南部和北部光化学生成的O3可以通过输送对整个东亚O3产生重要影响,并且在不同的季节呈现不同的特征。 相似文献
13.
我国对流层大气臭氧的数值模拟 总被引：7，自引：2，他引：7
本文建立了一个用于对流层大气臭氧模拟的三维欧拉模式,针对影响臭氧光化学转化的各种因素及我国城市光化学污染的特点,模式中简化了光化学项的计算。根据实际观测资料,提出了模拟云雾对臭氧影响的参数化方法,并确定了云雾作用系数,通过模式的数值模拟,得出了我国对流层大气臭氧,特别是近地面层大气臭氧的分布状况、我国城市光化学污染的分布特征以及它们的季节变化规律. 相似文献
14.
A Possible Photochemical Link Between Stratospheric and Near-Surface Ozone on Swiss Mountain Sites in Late Winter 总被引：2，自引：0，他引：2
Record high near-surface ozone concentrations at two elevated sites (Chaumont, 1140 m asl, and Rigi, 1030 m asl) in Switzerland were observed simultaneously with extremely low total ozone during a fair weather period in mid-February 1993. An analysis of ozone, temperature, humidity, and wind profiles suggests that the surface ozone peaks were most possibly generated within the region in a layer between about 1000 and 1500 m asl. Mean diurnal cycles of ozone concentration during the period shows a strong increase from late morning to late afternoon at Chaumont and at the same time a decrease at the high alpine site Jungfraujoch (3580 m asl). The different diurnal ozone cycles can both be explained photochemically by taking into account the large difference in NOx concentrations (about two orders of magnitude) between the sites. Photochemical processes are also indicated by the diurnal cycles of NO2 and NO concentration. As a strong photochemical activity is not expected in mid-February at 47°N, we hypothesize that the extremely low total ozone played a role. Total ozone controls the amount of UV-B radiation reaching the troposphere and thus influences photochemical processes. Using a radiation model, we calculated an increase in ozone photolysis at Chaumont and Jungfraujoch of 73% and 83%, respectively, on the day with the lowest total ozone (243 DU) compared to average February conditions (335 DU). It is suggested that total ozone changes have the potential to stimulate photochemistry sufficiently to produce the observed surface ozone peaks at Chaumont and Rigi of 61 and 64 ppbv, respectively. A fog layer just below Chaumont during these days probably also influenced photochemistry, but on a smaller spatial scale. Our empirical results on the influence of changing UV radiation on tropospheric photochemistry are in close agreement with model studies of other groups. Although this case study represents unique conditions, a distinct anticorrelation between near-surface ozone at Chaumont and total ozone also appears in other years (1992–1997) when selecting fair weather days in mid-February. However, other influences cannot be excluded. The selected days provide evidence of a significant photochemical source of ozone in the mid-latitude lower troposphere in late winter. 相似文献
15.
Michael Keller Daniel J. Jacob Steven C. Wofsy Robert C. Harriss 《Climatic change》1991,19(1-2):139-158
A major portion of tropospheric photochemistry occurs in the tropics. Deforestation, colonization, and development of tropical rain forest areas could provoke significant changes in emissions of radiatively and photochemically active trace gases. A brief review of studies on trace-gas emissions in pristine and disturbed tropical habitats is followed by an effort to model regional tropospheric chemistry under undisturbed and polluted conditions. Model results suggest that changing emissions could stimulate photochemistry leading to enhanced ozone production and greater mineral acidity in rainfall in colonized agricultural regions. Model results agree with measurements made during the NASA ABLE missions. Under agricultural/pastoral development scenarios, tropical rain forest regions could export greater levels of N2O, CH4, CO, and photochemical precursors of NO
y
and O3 to the global atmosphere with implications for climatic warming. 相似文献
16.
Nuria Castell Ariel F. Stein Enrique Mantilla Rosa Salvador Millán Millán 《Journal of Atmospheric Chemistry》2009,63(1):73-91
Understanding the chemical links between ozone (O3) and its two main precursors, nitrogen oxides (NOx) and volatile organic compounds (VOC), is important for designing effective
photochemical smog reduction strategies. This chemical relationship will determine which precursor (NOx or VOC) emission reduction
will be more effective for decreasing the ozone formation. Under certain conditions, ozone levels decrease as a result of
a reduction in NOx emissions but do not respond significantly to changes in VOC emissions (NOx-sensitive condition), while
under other conditions ozone concentrations decrease in response to reductions in VOCs and may even increase when NOx emissions
are reduced (VOC-sensitive conditions). Indicator species can be used to assess the sensitivity of ozone to changes in the
emissions of its precursors. These indicators are species or species ratios involved in ozone photochemistry which reflect
the primary chemical process through which the ozone was formed. In this work we use the MM5-CAMx model system to explore
the behaviour of various indicator species during two meteorological situations featuring different atmospheric conditions
in a complex terrain area. The results show that indicators based on nitrogen compounds (i.e,. NOy and NOz) are suitable for
defining the transition range from VOC- to NOx-sensitive chemistry, and that despite the uncertainties associated with the
use of chemical indicators, the ratios O3/NOy and O3/NOz may provide a simple and useful way to summarize the response of ozone to changes in NOx and VOC emissions in Southwestern
Spain. 相似文献
17.
The oxidation of nonmethane hydrocarbons represents a source of tropospheric ozone that is primarily confined to the boundary layers of several highly industrialized regions. (Each region has an area greater than one million km2). Using a photochemical model, the global tropospheric ozone budget is reexamined by including the in-situ production from these localized regimes. The results from these calculations suggest that the net source due to this photochemistry, which takes place on the synoptic scale, is approximately as large as the amount calculated for global scale photochemical processes which consider only the oxidation of methane and carbon monoxide. Such a finding may have a considerable impact on our understanding of the tropospheric ozone budget. The model results for ozone show reasonable agreement with the climatological summer distribution of ozone and the oxides of nitrogen at the surface and with the vertical distribution of ozone and nonmethane hydrocarbons obtained during a 1980 field program. 相似文献
18.
Black carbon(BC) reduces the photolysis coefficient by absorbing solar radiation, thereby affecting the concentration of ozone(O_3) near the ground. The influence of BC on O_3 has thus received much attention. In this study, Mie scattering and the tropospheric Ultraviolet and Visible radiation model are used to analyze the effect of BC optical properties on radiation. Combined with data of O_3 precursors in Nanjing in 2014, an EKMA curve is drawn, and the variations in O_3 concentration are further investigated using a zero-dimensional box mechanism model(NCAR MM). When O_3 precursors are unchanged, radiation and O_3 show a highly similar tendency in response to changing BC optical properties(R=0.997).With the increase of modal radius, the attenuation of fresh BC to radiation and O_3 first trends upward before decreasing. In the mixing process, the attenuation of BC to radiation and O_3 presents an upward tendency with the increase of relative humidity but decreases rapidly before increasing slowly with increasing thickness of coating. In addition, mass concentration is another major factor. When the BC to PM2.5 ratio increases to 5% in Nanjing, the radiation decreases by approximately 0.13%–3.71% while O_3 decreases by approximately 8.13%–13.11%. The radiative effect of BC not only reduces O_3 concentration but also changes the EKMA curve. Compared with the NOx control area, radiation has a significant influence on the VOCs control area. When aerosol optical depth(AOD) increases by 17.15%, the NOx to VOCs ratio decreases by 8.27%, and part of the original NOx control area is transferred to the VOCs control area. 相似文献