G20峰会期间长三角区域臭氧变化及管控效果评估

为了研究2016年二十国集团领导人峰会(G20峰会)期间长三角区域臭氧(O3)变化特征,评估管控措施对O3浓度的影响,利用2016年8月10日至9月20日杭州及周边地区的空气质量监测数据、气象数据以及排放清单数据,分析了O3和NO2浓度及气象条件的时空分布特征,研究了不同管控区域不同保障时期O3浓度的时空变化和O3敏感控制区的改变。结果表明:峰会保障期间对于一次排放污染物和细颗粒物的管控措施效果明显,但核心区的O3质量浓度高于严控区和管控区,分别高出11. 2、9. 2μg/m^3。日间的NOx管控导致O3日变化幅度增高接近50μg/m^3。在峰会保障期间,卫星数据和站点观测结果显示核心区O3由VOCs控制区转为NOx-VOCs协同控制区,整个长三角区域的O3生成对于NOx排放量更为敏感。管控措施越强,核心区的O3生成对于NOx排放越敏感,且O3浓度与NOx浓度的相关性越强。对NOx和VOCs的协同控制降低排放,是关系O3浓度管控的一项重要工作。     

Inventory of emissions of primary air pollutants in the city of Kocaeli, Turkey

This study aims to obtain a reliable inventory of the emission rates of the principal air pollutants including PM, SO2, NOx) and CO in Kocaeli, Turkey. In the first stage, the pollutant sources classified as point, area and line sources are determined in the area. Then the annual emission rates of the pollutants released from these sources are estimated by the emission factors given by USEPA and CORINAIR. Results show that the annual emission rates for PM, SO2, NOx) and CO are 2195 tons, 5342 tons, 14632 tons and 23095 tons, respectively. On the other hand, the pollutant group with the highest contribution to total emission rate is determined as the point sources for NOx, which is responsible for 73% of total NOx emission, while it is the area sources for PM, SO2 and CO with the contribution percentages of 75, 76 and 69, respectively.     

火力发电行业主要气态污染物排放量计算方法研究

针对目前我国火力发电行业气态污染物排放量计算方法使用混乱的情况,根据欧盟《空气污染物排放清单指南》和美国《空气污染物排放因子汇编》,介绍了火电行业主要气态污染物排放量的实际测量及理论计算方法。提出我国火电行业应根据实际情况,选择实际测量、排放因子或经验公式等方法计算污染物排放量;使用排放因子方法计算SO2排放量时,应开展S元素转化率的研究;火电厂应增加燃料中N元素的分析,以利于NOx排放量的准确估算。     

Simultaneous determination of atmospheric sulfur and nitrogen oxides using a battery-operated portable filter pack sampler

We developed a method to analyze atmospheric SO(x) (particulate SO(4)(2-)+ gaseous SO(2)) and NO(x) (NO + NO(2)) simultaneously using a battery-operated portable filter pack sampler. NO(x) determination using a filter pack method is new. SO(x) and NO(x) were collected on a Na(2)CO(3) filter and PTIO (2-phenyl-4,4,5,5-tetramethylimidazoline-3-oxide-1-oxyl) + TEA (triethanolamine) filters (6 piled sheets), respectively. Aqueous solutions were then used to extract pollutants trapped by the filters and the resulting extracts were pre-cleaned (e.g. elimination of PTIO) and analyzed for sulfate and nitrite by ion chromatography. Recoveries of SO(2) and NO(x) from standard pollutant gases and consistency of the field data with those from other instrumental methods were examined to evaluate our method. SO(x) and NO(x) could be analyzed accurately with determination limits of 0.2 ppbv and 1.0 ppbv (as daily average concentrations), respectively. The sampler can determine SO(x) and NO(x) concentrations at mountainous or remote sites without needing an electric power supply.     

集合数值预报系统在上海市空气质量预测预报中的应用研究

介绍了上海市世博环境空气质量集合数值预报系统的框架,分析了各模式在上海市空气质量预报及排放源污染贡献测算中的应用情况,提出开发多种预报手段、实施集合预报是提高城市空气质量预报准确率的发展方向。     

CO and NO2 pollution in a long two-way traffic road tunnel: investigation of NO2/NOx ratio and modelling of NO2 concentration

The CO, NO and NO2 concentrations, visibility and air flow velocity were measured using continuous analysers in a long Norwegian road tunnel (7.5 km) with traffic in both directions in April 1994 and 1995. The traffic density was monitored at the same time. The NO2 concentration exceeded Norwegian air quality limits for road tunnels 17% of the time in 1994. The traffic through the tunnel decreased from 1994 to 1995, and the mean NO2 concentration was reduced from 0.73 to 0.22 ppm. The ventilation fan control, based on the CO concentration only, was unsatisfactory and the air flow was sometimes low for hours. Models for NO2 concentration based on CO concentration and absolute air flow velocity were developed and tested. The NO2/NOx ratio showed an increase for NOx levels above 2 ppm; a likely explanation for this phenomenon is NO oxidation by O2. Exposure to high NO2 concentrations may represent a health risk for people with respiratory and cardiac diseases. In long road tunnels with two-way traffic, this study indicates that ventilation fan control based on CO concentration should be adjusted for changes in vehicle CO emission and should be supplemented by air flow monitoring to limit the NO2 concentration.     

上海浦东国际机场飞机尾气排放对机场附近空气质量的影响

统计2012年10月和11月浦东机场飞机机型和航班架次,根据各类飞机起降的污染物排放设计工作参数,估算出2012年浦东机场飞机起降时排放的NO2、SO2、CO和HC的估算值。利用浦东新区13个空气监测子站二氧化氮和二氧化硫数据绘制等值线图。结果显示,机场所在的江镇点位和祝桥点位二氧化氮浓度变化受飞机影响很大,而飞机排放的二氧化硫对两个点位的影响可以忽略不计。建议采用改进飞机滑行路线、探讨征收飞机碳排放税等措施减少飞机尾气排放对空气质量的影响。     

Determination of O3, NO2, SO2, CO and PM10 measured in Belgrade urban area

O(3), NO(2), SO(2), CO and PM(10) concentrations, simultaneously determined for the first time in Belgrade urban area in the autumnal period of 2005, are presented. The obtained results display similar behaviour of SO(2), NO(2), CO, PM(10) opposite from that of O(3). The weekend effect was also investigated showing diminution of average daily concentrations of SO(2), NO(2), PM(10) and CO for 72, 40, 37 and 42% respectively, and increase of the average daily concentration of O(3) for 56%. Influence of meteorological conditions on observed concentration levels was studied, too. The observed influence of wind speed on the O(3) nightly concentration levels was analyzed pointing to the phenomena of O(3) transport during episodic measurements. To make an identification of possible pollution sources and analyse the influence of meteorological parameters on pollution levels, air back trajectories for high level concentrations episodes were calculated and analysed. A multivariate receptor modelling (Principal Component Analysis, Cluster Analysis) has been applied to a set of data in order to determine the contribution of different sources. It was found that the main principal components, extracted from the air pollution data, were related to gasoline combustion, oil combustion and ozone transport.     

Air Quality and Monitoring Strategy in the Helsinki Metropolitan Area, Finland

The Helsinki Metropolitan Area Council (YTV) is responsible for air quality monitoring in the Helsinki area. Air quality has been monitored periodically since the late 1950s. An automatic SO2 monitoring network was constructed in 1975 and TSP measurements were added in 1978. Since then the network has been expanded and currently five automatic multicomponent stations form the basis of the network monitoring SO2, NO, NO2, CO, PM10 and O3 concentrations. Manual TSP and PM10 measurements are also conducted. Mobile monitoring units are also being used as well as special measurement campaigns. The effects of air pollution on nature are studied in bioindicator monitoring. An air quality index is used in order to inform the public of the current air quality situation. Changes in air quality are reflected in monitoring strategy. SO2 concentrations have decreased in the past two decades. Annual averages in 1995 were at or below 5 µg/m3. Traffic is the major source for pollutants even though catalytic converters have lowered traffic emissions somewhat. The highest annual average NO2 concentration at an urban site was 49 µg/m3 in 1995, and there has been no clear change in NO2 levels. There has been a decreasing trend in CO concentrations. Maximum annual TSP and PM10 averages in 1995 were 92 and 32 µg/m3, respectively. The highest average lead concentration was 0.01 µg/m3. Elevated concentrations are experienced from time to time. During the spring daily TSP and PM10 concentrations can go up to around 300 and 150 µg/m3, respectively. This is caused by resuspension mainly due to street sanding. Also a major winter NO2 episode occurred in December 1995. The highest hourly NO2 concentrations reached 400 µg/m3.     

Combined Non-Catalytic Reduction of NOx and SO2 by Ammonia Liquor during Staged Fluidized-Bed Combustion

Emissions of NOx and SO2 were monitored in the presence of ammonia liquor in a 0.09 m2 and 2 m high stainless-steel fluidized-bed combustor. Experiments were carried out at 2 m/s fluidizing velocity, 40% excess air, and 870 °C bed temperature. Ammonia liquor with 7% ammonia by weight was injected into the freeboard of the combustor 52 cm above the distributor through a water-cooled injector. A 65 : 34 primary/secondary air ratio was maintained throughout the investigation. Approximately 70% of NO and 20% of SO2 was reduced at an NH3/NO molar ratio of 2 : 1, respectively. However, a higher reduction in SO2 emissions (62%) was achieved at a very high NH3/NO molar ratio of 7 : 1. These experiments showed that ammonia addition did have a significant effect in SO2 reduction if injected in an excess amount. The injection of ammonia liquor combined with staged combustion was found to be very effective in reducing NOx emissions. A reduction of about 50% was achieved at an NH3/NO molar ratio of 0.6 : 1 which is also coupled with a very low level of ammonia in the flue.     

不同模式版本对长三角区域大气污染物模拟结果对比评估

选取2015年1、4、7、10月(分别代表冬、春、夏、秋4季),应用CMAQv4.7.1和CMAQv5.1模式模拟长三角区域的空气质量,对比了NO2、SO2、O3、PM2.54个常规污染物的模拟结果,表明CMAQv5.1对NO2、SO2和PM2.5的模拟效果优于CMAQv4.7.1,而CMAQv4.7.1的O3模拟效果优于CMAQv5.1;CMAQv5.1的NO2模拟值更接近地面观测值,比起不同版本的化学机制对NO2模拟效果的影响,NO2的模拟偏差受排放高估的影响更大;2个版本SO2的模拟值差距较小,且都与地面观测值之间差异较小;CMAQv5.1 PM2.5的模拟值比CMAQv4.7.1更接近观测值,气溶胶模块机制的更新(例如新增细分的PM2.5模式物种和部分二次有机气溶胶生成机制的改进等)对PM2.5模拟效果的改善显著;CMAQv5.1的O3模拟值比CMAQv4.7.1高,CMAQv5.1的O3模拟值在O3观测值的高值时段更接近观测值,而CMAQv4.7.1的O3模拟值在低值时段更接近观测值,CMAQv5.1在日最大8小时平均(MDA8)O3观测浓度超标日的O3模拟效果相比CMAQv4.7.1有一定程度的改善,但在非超标日模拟效果变差,CMAQv5.1的O3模拟效果总体相比CMAQv4.7.1并未得到有效提升。提出,未来针对低值时段和低值区域的O3模拟机制的改进将进一步提升O3模拟效果。     

Atmospheric deposition of major ions and trace metals near an industrial area,Jordan

Al, Cd, Cr, Cu, Fe, Mn, Pb, Zn, NH4+, Mg2+, Ca2+, Na+, K+, Cl-, NO3- and SO4(2-), along with pH were determined in wet and dry deposition samples collected at Al-Hashimya, Jordan. Mean trace metal concentrations were similar or less than those reported for other urban regions worldwide, while concentrations of Ca2+ and SO4(2-) were the highest. The high Ca2+ concentrations were attributed to the calcareous nature of the local soil and to the influence of the Saharan dust, while the high concentrations of SO4(2-) were attributed to the influence of anthropogenic sources and Saharan dust soil. Except for SO4(2-), NO3-, and Ca2+, dry deposition fluxes of measured metals and ions were higher than their corresponding wet deposition fluxes. The high annual average pH values recorded for wet and dry deposition samples were attributed to the neutralization of acidity by alkaline species. Cd, Cr, Cu, Pb, Zn, NO3- and SO4(2-) were enriched in wet and dry deposition samples relative to crustal material, and a significant anthropogenic contribution to these elements and ions is tentatively suggested. Finally, the possible sources and the main factors affecting the concentrations of the measured species are discussed.     

睢宁地区大气PM_(2.5)及气态污染物季节性变化特征

根据2014年全年实时在线观测数据,分析了徐州睢宁地区大气细颗粒物(PM_(2.5))和气态污染物(包括SO_2、CO、NO_x、O_3)质量浓度的季节性变化特征。结合后向轨迹模型,分析不同气团对该地区大气污染浓度的影响。PM_(2.5)与O_3值在夏季最低,呈显著相关,表明夏季PM_(2.5)主要受控于本地大气光化学活性。在冬季,除O_3外,PM_(2.5)、SO_2、CO、NO_x值最高,且大气颗粒物主要以细粒子为主。O_3在春季最高,并与远程传输的气团且经过我国东部污染源密集地区相对应。高浓度的PM_(2.5)主要与冬季缓慢移动的气团相对应,这可能将PM_(2.5)及其气态前体物传输至该地区进而加重大气污染程度。     

Characteristics of surface ozone at an urban site of Xi'an in Northwest China

Surface ozone concentrations in Xi'an, China were monitored from March 23, 2008 to January 12, 2009 using the Model ML/EC9810 ozone analyzer. The daily average O(3) ranged from <1 ppb to 64.2 ppbv with an annual average of 16.0 ppbv. The seasonal average of O(3) in summer (32.5 ppbv) was more than 10 times higher than that in winter (3.0 ppbv). A significant positive correlation was found between ozone concentration and ambient temperature, indicating that the intensity of solar radiation was one of the several major factors controlling surface ozone production. Using the NOAA HYSPLIT 4 trajectory model, the three longest O(3) pollution episodes were found to be associated with the high biogenic volatile organic carbon (BVOC) emissions from the vegetation of Qinling Mountains. No significant weekday and weekend difference in O(3) levels was detected due to the non-significant change in NO(x) emissions. O(3) depletion by NO emission directly emitted from vehicles, low oxygenated VOC concentrations, and low-level solar radiation caused by high aerosol loading all contributed to the low levels of O(3) found in Xi'an compared to other cities and rural areas.     

Surface ozone and meteorological condition in a single year at an urban site in central–eastern China

Surface ozone and some meteorological parameters were continuously measured from June 2003 to May 2004 at urban Jinan, China. The levels and variations of surface ozone were studied and the influences of meteorological parameters on ozone were analyzed. Annual and diurnal ozone variation patterns in Jinan both show a typical pattern for polluted urban areas. Daytime ozone concentrations in summer were the highest in the four seasons. However, during nighttime from 2100 to 0600 hours ozone concentrations in spring was higher than that in summer. Daily averaged ozone showed negative correlation with pressure and relative humidity and positive correlation with temperature, total solar radiation, sunshine duration and wind speed during the study period. Further studies show that, solar radiation is a primary influence factor for the daytime variations of ozone concentrations at this site; transport of pollutants by wind could enhance the pollution at this site; precipitation has a significant influence on decreasing surface ozone. A multi-day ozone episode from 16 to 21 June 2003 was observed at this site. Surface meteorological data analysis and backward trajectory computation show that the episode is associated with the influence of typhoon Soudelor, attributing to both local photochemical processes and transport of air pollutants from southeastern coastal region, especially Yangtze River Delta region.     

长三角城市群污染输送相互影响的敏感性试验

利用WRF-Chem模式,对2013年11月29日至12月11日长江三角洲地区的严重空气污染事件进行数值模拟,研究长三角核心区不同污染物本地源和外来输送所占比重。分析长三角核心区排放源对本地不同污染物浓度的污染贡献。结果表明,在2013年12月的这一次污染事件中,颗粒物平均本地贡献与外来输送基本比重相当;而SO_2、CO、NH_3、NO_x这4种气体污染物则以本地贡献为主,本地贡献的差异与气体的化学反应活性有关,活性越强本地贡献比重越大。污染过程中12月7日至12月9日00:00为污染最严重的时段,污染物的本地贡献有明显上升。区域间输送的方向和强度与地面风向、风速有紧密的联系。在边界层高度范围内,大部分污染物越往高空本地排放源的贡献越弱,外来输送主导作用增强,而硝酸盐在地面、1 km和1.5 km的本地贡献差异远小于其他污染物。     

空气质量多模式预报系统在中山市的应用

介绍了中山市空气质量多模式预报系统。对2015年3月—2016年2月的预报效果评估表明:系统可以较好地反映污染物的变化趋势但仍存在系统性偏差。通过对排放源清单的调整优化及对模式干沉降模块的改进使模式系统的偏差显著减小。总结并建立中山市污染天气案例库,发现在典型污染天气形势下,除O3-8 h外,其他污染物均值均能达到空气质量二级标准。未来将从2个方面提高中山市空气质量预报预警系统的实用性,包括逐步实现污染源排放清单的动态及时更新和提高极端气象条件下O3污染预报能力。     

Characterization and diurnal variation of size-resolved inorganic water-soluble ions at a rural background site

Water-soluble inorganic ions in aerosol samples have been studied. The sample collection took place during summer in 2003 at a European background site which is operating within the framework of the European Monitoring and Evaluation Program. Gent type PM10 stacked filter unit (SFU) samplers were operated in parallel on a day and night basis to collect particles in separate coarse (2.0-10 microm) and fine (<2.0 microm) size fractions. Particulate masses were measured gravimetrically; the filters from one of the SFU samplers were analyzed by particle-induced X-ray emission spectrometry (PIXE) and instrumental neutron activation analysis (INAA). Filters from the other SFU sampler were analyzed by ion chromatography (IC) for major inorganic anions (MSA-, NO2(-), NO3(-), Cl-, Br-, SO4(2-), oxalate) and cations (Na+, K+, NH4(+), Mg2+, Ca2+). The water-soluble inorganic ions measured were responsible for 44% and 16% of the total fine and coarse particulate mass, respectively. In the fine size fraction, the main ionic components were SO4(2-) and NH4(+) accounting for about 90% of fine ionic mass. In the coarse fraction the main ionic components were Ca2+ and NO3(-), followed by SO4(2-). Significant day and night difference in the mass concentrations was observed only for fine NO3(-). The molar ratios of fine NH4(+) to SO4(2-) indicated their complete neutralization to (NH4)2SO4. According to the cation-to-anion ratios the coarse particles were alkaline, while the fine particles were slightly acidic or neutral. By comparing the corresponding concentrations obtained from PIXE/INAA and IC, we determined the water-extractable part of the individual species. We also investigated the effect of long-range transported air masses on the local air concentrations, and we found that the air quality of this background monitoring station was affected by regional pollution sources.     

A novel wet-scrubbing process using Fe(VI) for simultaneous removal of SO2 and NO

The objective of this work was to develop a novel wet-scrubbing process using Fe(VI) for the simultaneous removal of gaseous NO and SO(2). The oxidation of SO(2) and NO with Fe(VI) was studied in aqueous solution at alkaline pH (9.0-11.0). A stoichiometric molar ratio for NO and SO(2) oxidation with Fe(VI) was determined to be nearly 3.0. Sulfate and nitrate was identified as final products by ion chromatography from the reaction at pH 9.0-11.0. The feasibility of simultaneous removal of multiple gas pollutants with the continuous feeding of ferrate in lab-scale was investigated from the view of industrial application. It was found that the removal efficiency of NO and SO(2) was enhanced with the increase of Fe(VI) concentration, more than 90% NO removal efficiency and 100% SO(2) removal efficiency were achieved by wet-scrubbing process using Fe(VI) at room temperature and ambient atmosphere. The results demonstrate that Fe(VI) could be an effective wet-scrubbing agent for the simultaneous removal of NO and SO(2).