Composition, seasonal variation, and sources of PM10 from world heritage site Taj Mahal, Agra

Air samples for PM(10) (dp?相似文献   

宁波和温州地区夏季大气中不同粒径颗粒物特征分析

对宁波地区北仑和奉化站、温州地区乐清站3个监测点夏季TSP、PM10、PM2.5和PM1.0进行监测,测试分析各种粒径颗粒物浓度水平和粒径分布特征,并通过化学质量平衡(CMB)受体模型对颗粒物进行源解析。监测结果显示,夏季宁波、温州地区TSP和PM10日均浓度为0.049～0.134mg/m3和0.025～0.084mg/m3,均未超过我国环境空气质量二级标准;PM2.5日均浓度为0.007～0.069mg/m3,按美国2006年EPA最新标准限值0.035mg/m3衡量,奉化、乐清、北仑站的超标天数占总监测天数的比例分别为75%、40%和37.5%。粒径分布统计结果显示,3个监测站点PM10占TSP的比例为48.78%～86.96%;PM2.5占TSP的比例为33.33%～72.46%;奉化和乐清监测点PM10中PM2.5和PM1.0的比例平均值在50%以上。源解析结果显示,夏季TSP主要来源于土壤尘,其次是建筑尘和煤烟尘,其贡献率分别为40.70%～55.49%、9.62%～13.64%和5.85%～17.28%。     

Dry deposition study by using dry deposition plate and water surface sampler in Shalu, central Taiwan

This study presents the chemical composition of dry deposition by using dry deposition plate and water surfaces sampler during daytime and nighttime sampling periods at a near highway traffic sampling site. In addition, the characterization for mass and water soluble species of total suspended particulate (TSP), PM2.5 and PM10 were also studied at this sampling site during August 22 to October 31 of 2006 around central Taiwan. The samples collected were analyzed by using Ion Chromatography (DIONEX 100) for the ionic species analysis. Results of the particulate dry deposition fluxes are higher in the water surfaces sampler than that of the dry deposition plate. In other words, the results also indicated that water surface can absorb more ambient dry deposition inorganic pollutants than that of dry deposition plate in this study. The results obtained in this study indicated that the ionic species of Cl(-), NO3(-) and SO4(2-) occupied about average 60-70% downward flux out of total ionic species for either dry deposition plate or water surfaces sampler during August to October of 2006 at this near highway traffic sampling site.     

Atmospheric aerosol concentration level and chemical characteristics of water-soluble ionic species in wintertime in Beijing,China

Total suspended particulate (TSP) samples were collected during wintertime from November 24, 1998 to February 12, 1999 in Beijing. Ionic species including Cl-, NO3(-), SO4(2-), Na+, NH4(+), K+, Mg2+ and Ca2+ were determined by Ion Chromatography (IC). The sum average concentration of all the determined ions accounted for 18.9% of the TSP concentration, and SO4(2-) appeared the dominant ion with an average concentration of 30.84 microg m(-3); the sum mass concentration of SO4(2-), NO3(-), Ca2+ and NH4(+) accounted for about 83.2% of all the eight ions measured. The study indicated that the chemical form of sulfate and ammonium varies with TSP concentration levels. During heavy pollution periods, the average TSP concentration was 0.66 mg m(-3), and the NH4(+)/SO4(2-) molar ratio was low (0.58). It indicated that sulfate may present as CaSO4 and (NH4)2SO4 x CaSO4 x 2H2O. When TSP concentration (average 0.186 mg m(-3)) was relatively low, the NH4(+)/SO4(2-) molar ratio was 1.94, close to the theoretical ratio of 2 of (NH4)2SO4. Under this condition (NH4)2SO4 is expected to exist as the major form of sulfate. When the TSP concentration level was medium (average 0.35 mg m(-3)), the NH4+/SO4(2-) molar ratio appeared an average value (1.27), (NH4)2SO4, (NH4)2SO4 x CaSO4 x 2H2O and CaSO4 are expected to be present in those aerosol particles. Meteorological conditions including wind speed and wind direction were related to the TSP concentration level.     

Short-term variation in air quality associated with firework events: a case study

The effect of fireworks on air quality was assessed from the ambient concentrations of various air pollutants (SO2, NO2, PM10 and TSP) during Diwali festival in Hisar city (India), in November 1999. The extensive use of fireworks was found to be related to short-term variation in air quality. During the festival the concentration of SO2 was observed to be increased approximately 10-fold at few sites, whereas the concentrations of NO2, PM10 and TSP increased 2-3 times, compared to the data collected on a typical winter day in December 1999. The maximum NO2 concentration was observed a day after the festival. The diurnal pattern of the above pollutants showed a slight increase in the night. The levels of these pollutants observed during Diwali were found to be moderately high, which can be associated with serious health impacts.     

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.     

广州市灰霾期PM10的化学组成对能见度的影响

采集广州市大气可吸入颗粒物(PM10)样品,并分别对冬、夏两季灰霾和非灰霾期PM10中有机碳(OC)、元素碳(EC)和水溶性离子进行分析。广州市灰霾期大气PM10中的主要化学成分按质量浓度大小排序为OC>NO3->SO24->NH4+>EC(非灰霾期则依次为OC>SO24->EC>NH4+>NO3-),其质量浓度分别为非灰霾期的4.7、12.5、3.7、3.2和2.3倍。相关性分析表明,灰霾期总碳[TC(OC+EC)]及NO3-的质量浓度对大气能见度的降低起主要作用,而非灰霾期则主要是TC和SO24-。     

Characteristics of aerosol types during large-scale transport of air pollution over the Yellow Sea region and at Cheongwon,Korea, in 2008

Episodes of large-scale transport of airborne dust and anthropogenic pollutant particles from different sources in the East Asian continent in 2008 were identified by National Oceanic and Atmospheric Administration satellite RGB (red, green, and blue)-composite images and the mass concentrations of ground level particulate matter. These particles were divided into dust, sea salt, smoke plume, and sulfate by an aerosol classification algorithm. To analyze the aerosol size distribution during large-scale transport of atmospheric aerosols, aerosol optical depth (AOD) and fine aerosol weighting (FW) of moderate imaging spectroradiometer aerosol products were used over the East Asian region. Six episodes of massive airborne dust particles, originating from sandstorms in northern China, Mongolia, and the Loess Plateau of China, were observed at Cheongwon. Classified dust aerosol types were distributed on a large-scale over the Yellow Sea region. The average PM10 and PM2.5 ratio to the total mass concentration TSP were 70% and 15%, respectively. However, the mass concentration of PM2.5 among TSP increased to as high as 23% in an episode where dust traveled in by way of an industrial area in eastern China. In the other five episodes of anthropogenic pollutant particles that flowed into the Korean Peninsula from eastern China, the anthropogenic pollutant particles were largely detected in the form of smoke over the Yellow Sea region. The average PM10 and PM2.5 ratios to TSP were 82% and 65%, respectively. The ratio of PM2.5 mass concentrations among TSP varied significantly depending on the origin and pathway of the airborne dust particles. The average AOD for the large-scale transport of anthropogenic pollutant particles in the East Asian region was measured to be 0.42 ± 0.17, which is higher in terms of the rate against atmospheric aerosols as compared with the AOD (0.36 ± 0.13) for airborne dust particles with sandstorms. In particular, the region ranging from eastern China, the Yellow Sea, and the Korean Peninsula to the Korea East Sea was characterized by high AOD distributions. In the episode of anthropogenic polluted aerosols, FW averaged 0.63 ± 0.16, a value higher than that in the episode of airborne dust particles (0.52 ± 0.13) with sandstorms, showing that fine anthropogenic pollutant particles contribute greatly to atmospheric aerosols in East Asia.     

The Effect of Traction Sanding on Urban Suspended Particles in Finland

Springtime urban road dust forms one of the most serious problems regarding air pollution in Finland. The composition and origin of springtime dust was studied in southern Finland with two different methods. Suspended particles (PM10 and TSP) were collected with high volume particle samplers and particle deposition was collected with moss bags. The composition of the PM(1.5-10) fraction was studied using individual particle analysis with SEM/EDX. The deposition in the moss bags was analysed with ICP-MS. The results showed that during the study period, approximately 10% of both PM(1.5-10) particles and the deposition originated from sanding. Other sources in the springtime PM(1.5-10) were e.g. asphalt aggregate or soil and combustion processes. It can be concluded that sanding produced a relatively small amount of particulate matter under the investigated circumstances.     

北京市大气颗粒物的浓度水平和离子物种的化学形态

用离子色谱法测定了 1 998年 1 1月至 1 999年 2月期间的 2 4个总悬浮颗粒物 (TSP)样品中 NH+ 4、NO- 3、SO2 - 4和Na+ 质量浓度。研究结果表明 ,北京市冬季大气颗粒物中离子物种的化学形态可以分为三种情况 :污染严重时 ,离子物种以 H2 SO4 、NH4 HSO4 、Na NO3为主要存在形态 ,气溶胶酸性强 ;污染轻时 ,离子物种以 (NH4 ) 2 SO4 、Na NO3为主要存在形态 ,气溶胶呈弱酸性 ;中等污染时 ,离子物种以 (NH4 ) 2 SO4 、NH4 HSO4 、Na NO3几种化学形态存在 ,气溶胶呈中等酸性     

Study on Size Distribution of Total Aerosol and Water-Soluble Ions During an Asian Dust Storm Event at Jeju Island, Korea

Soil dust particles transported from loess regions of the Asian continent, called Asian dust, highly influences the air quality of north-eastern Asia and the northern Pacific Ocean. In order to investigate the effects of these dust storms on the chemical composition of atmospheric aerosol particles with different size, measurements of size distributions of total aerosol and major ion species were carried out on Jeju Island, Korea during April 2001. Juju Island was chosen for the study because the levels of emissions of anthropogenic air pollutants are very low. A 5-stage cascade impactor was used to sample size-fractionated aerosol particles. Samples were analyzed for major water-soluble ions using Dionex DX-120 ion chromatograph. The average mass concentration of total aerosol was found to be 24.4 and 108.3 microg m(-3) for non-Asian dust and Asian dust periods, respectively. The total aerosol size distribution, measured during the non-Asian dust period, was bimodal, whereas the coarse particles dominated the size distribution of total aerosol during the Asian dust period. It was found that SO4(2-), NH4+ and K+ were mainly distributed in fine particles, while Cl-, NO3-, Na+, Mg2+ and Ca2+ were in coarse particles. Although SO4(2-) was mainly distributed in fine particles, during the Asian dust period, the concentrations in coarse particles were significantly increased. This indicates heterogeneous oxidation of SO2 on wet surfaces of basic soil dust particles. The NH4+ was found to exist as (NH4)2SO4 in fine particles, with a molar ratio of NH4+ to SO4(2-) of 2.37 and 1.52 for non-Asian dust and Asian dust periods, respectively. Taking into account the proximity of the sampling site to the sea, and the observed chloride depletion, coarse mode nitrate, during the non-Asian dust period, is assumed to originate from the reaction of nitric acid with sodium chloride on the surfaces of sea-salt particles although the chloride depletion was not shown to be large enough to prove this assumption. During the Asian dust period, however, chloride depletion was much smaller, indicating coarse nitrate particles were mainly produced by the reaction of nitric acid with surfaces of basic soil particles. Most chloride and sodium components were shown to originate from sea-salt particles. Asian dust aerosols, arriving at Jeju Island, contained considerable amounts of sea-salt particles as they passed over the Yellow Sea. Ca2+ was shown to be the most abundant species in Asian dust particles.     

Sixteen-year air quality data analysis of a high environmental risk area in Southern Italy

The Brindisi area is characterized by the presence of industries with high environmental impact, located along its eastern border. Epidemiological studies have revealed several critical situations: two short-term (2003-2005) epidemiological studies have shown that PM(10) and NO(2) are adversely associated with daily hospital admissions: one of the two pointed to the associations with wind blowing from the southern, eastern and western sectors. This study aims to expand the time span of available air quality data in order to provide a more complete and extensive epidemiological study. Multi-year series (from 1992 to 2007) of SO(2), NO(2), and TSP concentration data are presented and analyzed. Data show a significant downward trend of SO(2) from 1992 to 2007, while for the TSP series, the downward trend is limited to the period 1992-1994. Marked seasonal trends are evident for all three pollutants, especially for NO(2) and TSP. The NO(2) series shows higher levels in winter. Inversely, the TSP series shows its maximum values during the summer months, associated with a moderate correlation with temperature and a poor correlation with other pollutants. Analysis of the series for wind sectors revealed the influence of the industrial site and of the harbor. The concentration series exhibit high concentration values and stronger correlations between them and with meteorology for wind blowing from the eastern sectors. Overall analysis supports the hypothesis of a different origin for TSP during the year and for different wind regimes and therefore possible size and chemical differences in TSP, which should be further investigated due to their health implications.     

Characteristics of Hazardous Airborne Dust Around an Indian Surface Coal Mining Area

Surface coal mining creates more air pollution problems with respect to dust than underground mining . An investigation was conducted to evaluate the characteristics of the airborne dust created by surface coal mining in the Jharia Coalfield. Work zone air quality monitoring was conducted at six locations, and ambient air quality monitoring was conducted at five locations, for a period of 1 year. Total suspended particulate matter (TSP) concentration was found to be as high as 3,723 μg/m³, respirable particulate matter (PM10) 780 μg/m³, and benzene soluble matter was up to 32% in TSP in work zone air. In ambient air, the average maximum level of TSP was 837 μg/m³, PM10 170 μg/m³ and benzene soluble matter was up to 30%. Particle size analysis of TSP revealed that they were more respirable in nature and the median diameter was around 20 μm. Work zone air was found to have higher levels of TSP, PM10 and benzene soluble materials than ambient air. Variations in weight percentages for different size particles are discussed on the basis of mining activities. Anionic concentration in TSP was also determined. This paper concludes that more stringent air quality standards should be adopted for coal mining areas and due consideration should be given on particle size distribution of the air-borne dust while designing control equipment.     

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.     

乌鲁木齐市采暖季空气质量变化趋势分析

为了定量评价乌鲁木齐市采暖季空气污染近五年的治理成效,给环境治理决策提供科学依据,运用回归分析方法,对乌鲁木齐市采暖季空气质量的浓度、级别和变化规律进行回归分析。分析结果表明,PM10、SO2、NO2三项污染物的浓度都有所下降,空气质量级别的污染天数呈现明显的月变化规律。乌鲁木齐市采暖季空气的重污染状况有所遏制,但SO2污染凸现,在下一步的治理工作中,加强尘污染治理的同时要加大对SO2的治理力度。     

2008年春季呼和浩特沙尘天气与TSP和PM_(10)污染的关系

利用TSP和PM10逐时监测数据,对2008年春季呼和浩特市TSP和PM10浓度的变化及其在沙尘天气过程中的相关性进行了分析,结果表明:(1)2008年春季TSP和PM10浓度值多高于国家环境空气质量二级标准,沙尘天气是影响空气环境质量的主要诱因。(2)TSP和PM10浓度在沙尘暴发生当日及前后几天均会有不同程度的增加,且以沙尘天气发生当日浓度最大。TSP和PM10浓度3月份最低,4月份次之,5月份最高。(3)不同沙尘天气过程中,TSP和PM10浓度相差明显,且TSP与PM10/TSP值随沙尘天气强度的增加而增大,PM10在不同沙尘天气过程中均为主要组成成分。(4)沙尘天气过程中TSP与PM10呈线性相关。     

PM source apportionment and trace metallic aerosol affinities during atmospheric pollution episodes: a case study from Puertollano, Spain

Source apportionment study was performed, applying principal component analysis to the results of 221 chemical analyses of PM10 and PM2.5 samples collected daily from the industrial (but low traffic) Spanish town of Puertollano over a 14-month period during 2004-2005. Results reveal compositional variations attributable to different mixtures of natural and anthropogenic materials, mainly soil and rock dust (crustal), marine salt (only in PM10), petrochemical refinery emissions, and particles attributed to the combustion of local coal, which is unusually rich in Pb and Sb. During the study period there were 34 pollution episodes when PM10 exceeded 50 tg m(-3), mostly due to winter air temperature inversions, regional atmospheric stagnation, or African dust incursions (North African, NAF days: usually in summer). Whereas the crustal component during NAF episodes averaged 52% with a PM2.5/PM10 ratio of 0.54, this dropped to 29% and a PM2.5/PM10 of 0.67 during non-NAF days when anthropogenic materials predominated. Abnormally enhanced concentrations of pathfinder metallic trace elements provide additional evidence for source apportionment: thus aerosols with raised levels of Pb and Sb are associated with local coal combustion, Ni and V can be linked to petrochemical PM emissions, and Ti, Mn, Rb, and Ce are particularly characteristic of crustal dust incursions.     

Source apportionment of PM10 and PM(2.5) at Tocopilla, Chile (22 degrees 05' S, 70 degrees 12' W)

Tocopilla is located on the coast of Northern Chile, within an arid region that extends from 30 degrees S to the border with Perú. The major industrial activities are related to the copper mining industry. A measurement campaign was conducted during March and April 2006 to determine ambient PM10 and PM(2.5) concentrations in the city. The results showed significantly higher PM10 concentrations in the southern part of the city (117 microg/m3) compared with 79 and 80 (microg/m3) in the central and northern sites. By contrast, ambient PM2.5 concentrations had a more uniform spatial distribution across the city, around 20 (microg/m3). In order to conduct a source apportionment, daily PM10 and PM(2.5) samples were analyzed for elements by XRF. EPA's Positive Matrix Factorization software was used to interpret the results of the chemical compositions. The major source contributing to PM(2.5) at sites 1, 2 and 3, respectively are: (a) sulfates, with approximately 50% of PM2.5 concentrations at the three sites; (b) fugitive emissions from fertilizer storage and handling, with 16%, 21% and 10%; (c) Coal and residual oil combustion, with 15%, 15% and 4%; (d) Sea salt, 5%, 6% and 16%; (e) Copper ore processing, 4%, 5% and 15%; and (f) a mixed dust source with 11%, 7% and 4%. Results for PM10--at sites 1, 2 and 3, respectively--show that the major contributors are: (a) sea salt source with 36%, 32% and 36% of the PM10 concentration; (b) copper processing emissions mixed with airborne soil dust with 6.6%, 11.5% and 41%; (c) sulfates with 31%, 31% and 12%; (d) a mixed dust source with 16%, 12% and 10%, and (e) the fertilizer stockpile emissions, with 11%, 14% and 2% of the PM10 concentration. The high natural background of PM10 implies that major reductions in anthropogenic emissions of PM10 and SO2 would be required to attain ambient air quality standards for PM10; those reductions would curb down ambient PM(2.5) concentrations as well.     

上海浦东新区环境空气质量特点及成因分析

为了解浦东新区建区以来的环境空气质量，浦东新区环境保护监测站对1994年－2001年环境空气中主要污染物监测结果进行了分析：SO2，NOx,TSP的质量浓度和分指数结果相比较，TSP占有最大权重，处于污染主导地位，其主要污染源为工业粉尘，烟尘，机动车排放的尾气，建筑施工及道路交通产生的尘污染。     

2017年厦门金砖会晤期间PM2.5的化学特征及来源

为了探讨厦门金砖会晤期间的排放控制措施以及天气形势对大气颗粒物污染特征的影响,于2017年8月10日至9月10日对厦门气态污染物、细颗粒物(PM2.5)中的水溶性离子以及有机碳(OC)、元素碳(EC)等主要化学成分开展了高时间分辨率的在线监测。根据空气质量管控措施和天气形势将研究期分为6个阶段。管控前、管控期Ⅰ(非台风)和管控期Ⅱ(非台风) PM2.5质量浓度分别为(33. 12±9. 48)、(30. 30±17. 00)、(16. 01±4. 71)μg/m^3。管控期Ⅰ(台风)和管控期Ⅱ(台风) PM2.5质量浓度分别为(12. 40±3. 73)、(12. 45±3. 28)μg/m^3。结果表明:管控期Ⅰ(非台风)阶段受静稳天气的影响,管控效果削弱,PM2.5质量浓度下降幅度小;台风对颗粒物质量浓度下降的影响比管控更显著。管控初期,PM2.5中二次无机离子的质量浓度下降明显;台风对碳质组分质量浓度的影响不如无机组分显著。PMF源解析结果表明,二次无机源是PM2.5主要来源,随着管控措施的实行,扬尘源的贡献从21%降低到6%,而机动车源的贡献降幅不明显。台风期间SO4^2-、NO3^-、SO2、NO2以及硫酸盐氧化比值(SOR)均明显低于非台风期间,氮氧化比值(NOR)反而升高。台风和非台风期间NOR的日变化特征一致,NOR与阳离子的相关性分析结果表明,台风或高风速海风期间NOR与Na^+呈现很强的正相关性,说明海盐粒子可促进NO2非均相反应生成NO3-。