Chemical Composition and Sources of PM10 and PM2.5 Aerosols in Guangzhou, China

Aerosol samples of PM10 and PM2.5 are collected in summertime at four monitoring sites in Guangzhou, China. The concentrations of organic and elemental carbons (OC/EC), inorganic ions, and elements in PM10 and PM2.5 are also quantified. Our study aims to: (1) characterize the particulate concentrations and associated chemical species in urban atmosphere (2) identify the potential sources and estimate their apportionment. The results show that average concentration of PM2.5 (97.54 μg m⁻³) in Guangzhou significantly exceeds the National Ambient Air Quality Standard (NAAQS) 24-h average of 65 μg m⁻³. OC, EC, Sulfate, ammonium, K, V, Ni, Cu, Zn, Pb, As, Cd and Se are mainly in PM2.5 fraction of particles, while chloride, nitrate, Na, Mg, Al, Fe, Ca, Ti and Mn are mainly in PM2.5-10 fraction. The major components such as sulfate, OC and EC account for about 70–90% of the particulate mass. Enrichment factors (EF) for elements are calculated to indicate that elements of anthropogenic origins (Zn, Pb, As, Se, V, Ni, Cu and Cd) are highly enriched with respect to crustal composition (Al, Fe, Ca, Ti and Mn). Ambient and source data are used in the multi-variable linearly regression analysis for source identification and apportionment, indicating that major sources and their apportionments of ambient particulate aerosols in Guangzhou are vehicle exhaust by 38.4% and coal combustion by 26.0%, respetively.     

Risk assessment of heavy metals in road and soil dusts within PM2.5, PM10 and PM100 fractions in Dongying city, Shandong Province, China

15 road and 14 soil dust samples were collected from an oilfield city, Dongying, from 11/2009-4/2010 and analyzed by inductively coupled plasma-mass spectroscopy (ICP-MS) for V, Cr, Mn, Co, Ni, Cu, Zn, As, Cd and Pb within PM(2.5), PM(10) and PM(100) fractions synchronously. Metal concentrations, sources and human health risk were studied. Results showed that both soil and road dust exhibited higher values for Mn and Zn and lower values for Co and Cd for the three fractions. Mass concentration ratios of PM(2.5)/PM(10) and PM(10)/PM(100) for metals in road and soil dust indicate that most of the heavy metals tend to concentrate in fine particles. Geoaccumulation index and enrichment factors analysis showed that Cu, Zn and Cd exhibited moderate or heavy contamination and significant enrichment, indicating the influence of anthropogenic sources. Vanadium, Cr, Mn and Co were mostly not enriched and were mainly influenced by crustal sources. For Ni, As and Pb, they ranged from not enriched to moderately enriched and were influenced by both crustal materials and anthropogenic sources. The conclusions were confirmed by multivariate analysis methods. Principle component analysis revealed that the major sources were vehicle emission, industrial activities, coal combustion, agricultural activities and crustal materials. The risk assessment results indicated that metal ingestion appeared to be the main exposure route followed by dermal contact. The most likely cause for cancer and other health risks are both the fine particles of soil and road dusts.     

Analysis of a high PM10 episode observed at a coastal site nearby Shanghai, China

A high PM₁₀ episode observed at a coastal site nearby Shanghai during 18–19 January 2007 was analyzed in this study. The maximum hourly averaged PM₁₀ concentrations for the 2 days were 0.58 and 0.62 mg/m³, respectively. The meteorological condition during the episode was favorable for air pollution with large-scale stagnation. There was no dispersing effect by high wind, no scavenging function by precipitation, and no diluting process by clean marine air during the episode. The trajectories for 16–19 January all came from the northern region and kept in low levels, and during the episode peak time, from the morning of 18 to the morning of 19 January, trajectories all came from the northern inland areas and had passed over the coastal region of Jiangsu province before arriving at the site. The variation of the air pollution indexes (APIs) in the cities located in the upwind direction of the site during the episode days clearly shows a process of large-scale air pollution from north to south. The liner correlation coefficient for PM₁₀ and SO₂ concentrations is 0.774 during the episode, while for PM₁₀ and CO, it even reaches 0.995, which indicated that the high PM₁₀ was mainly emitted from the coal burning for domestic heating in winter. Therefore, the observed episode was caused by the transport of domestic heating pollutants accumulated in the boundary layer from northern continental areas.     

Gravimetric and Chemical Features of Airborne PM10 AND PM2.5 in Mainland Portugal

This paper describes concentration amounts of arsenic (As), particulate mercury (Hg), nickel (Ni) and lead (Pb) in PM₁₀ and PM_2.5, collected since 1993 by the Technological and Nuclear Institute (ITN) at different locations in mainland Portugal, featuring urban, industrial and rural environments, and a control as well. Most results were obtained in the vicinity of coal- and oil-fired power plants. Airborne mass concentrations were determined by gravimetry. As and Hg concentrations were obtained through instrumental neutron activation analysis (INAA), and Ni and Pb concentrations through proton-induced X-ray emission (PIXE). Comparison with the EU (European Union) and the US EPA (United States Environmental Protection Agency) directives for Ambient Air has been carried out, even though the sampling protocols herein – set within the framework of ITN's R&D projects and/or monitoring contracts – were not consistent with the former regulations. Taking this into account, 1) the EU daily limit for PM₁₀ was exceeded a few times in all sites except the control, even if the number of times was still inferior to the allowed one; 2) the EU annual mean for PM₁₀ was exceeded at one site; 3) the EPA daily limit for PM_2.5 was exceeded one time at three sites; 4) the EPA annual mean for PM_2.5 was exceeded at most sites; 5) the inner-Lisboa site approached or exceeded the legislated PMs; 6) Pb levels stayed far below the EU limit value; and 7) concentrations of As, Ni and Hg were also far less than the reference values adopted by EU. In every location, Ni appeared more concentrated in PM_2.5 than in coarser particles, and its levels were not that different from site to site, excluding the control. The highest As and Hg concentrations were found in the neighbourhood of the coal-fired, utility power plants. The results may be viewed as a “worst-case scenario” of atmospheric pollution, since they have been obtained in busy urban-industrial areas and/or near major power-generation and waste-incineration facilities.     

Characterization of metal aerosols in PM10 from urban, industrial, and Asian Dust sources

Metallic elements (As, Be, Ca, Cd, Co, Cr, Fe, K, Mn, Ni, Pb, Sb, Se, and Zn) in PM10 aerosols were determined at urban and industrial sites, which are affected by traffic and residential sources, metallurgical activity, and petrochemical and steel works. The effect of the long-range transported Asian Dust on the metal content of aerosols was also examined. At the urban sampling site, concentrations of As, Cd, Pb, Se, and Zn were assigned to road traffic and combustion sources, Ca and Fe to soil dust sources from long-range transported Asian Dusts, and Cr and Ni to metallurgical sources transported from the nearby industrial complex, based on Principal Component Analysis (PCA). Enhanced Cr and Ni concentrations at the metallurgical industrial site suggest that local emissions from metal-assembly facilities and manufacture of alloys contributed to elevated levels of those metals. We also observed that petrochemical activities contributed to increased levels of Sb and Zn. When Asian Dust events occurred, Ca, Fe, K, and Zn concentrations dramatically increased compared to values without the Asian Dust. Two different types of Asian Dust events were observed. For the Asian Dust event 1 (4/1/2007), the Fe and K concentrations were much higher by a factor of 2–3 than those for the Asian Dust event 2 (3/2/2008), while As, Mn, and Zn concentrations were significantly higher on the Asian Dust event 2. Backward trajectory analysis showed that for the Asian Dust event 2, the air mass had passed over the heavily industrialized zones in China during long-range transport to the current sampling site, suggesting that the As, Mn, and Zn may have originated from industrial sources.     

Chemical composition of precipitation and its sources in Hangzhou, China

To understand the origin and chemical characteristics of precipitation in Hangzhou, rainwater samples were collected from June 2006 to May 2008. All samples were analyzed for pH, electrical conductivity, and major ions (NH??, Ca2?, Mg2?, Na?, K?, SO?2?, NO??, F?, and Cl?). Acidification of precipitation in Hangzhou was serious with volume-weighted mean pH value of 4.5, while frequency of acid rain was 95%. The calculated SO?2?/NO?? ratio in Hangzhou precipitation was 2.87, which indicated that the precipitation of Hangzhou belonged to sulfate-based acid rain. The results of acid neutralization analysis showed that not all the acidity in the precipitation of Hangzhou was neutralized by alkaline constituents. The results of sea salt contribution analysis showed that nearly all SO?2?, Ca2?, and Mg2? and 33.7% of K? were of non-sea origins, while all Na? and Cl? and 66.3% of K? originated from sea sources. The principal component analysis which was used to analyze the sources of various ions indicated that chemical compositions of precipitation in Hangzhou mainly came from terrestrial sources, factory emissions, fuel wood burning, and marine sources.     

柳州市大气颗粒物中多环芳烃的种类和时空分布特征及来源

采用气相色谱/质谱联用技术(GC/MS)检测了柳州市大气颗粒物样品中的PAHs,比较了柳州市各区大气颗粒物中多环芳烃含量的差异以及不同季节对多环芳烃含量的影响,讨论了其分布规律及污染源.     

广州大型购物中心室内空气中PM10、CO和CO2的分布和来源特征

利用便携式测量仪,对广州市大型购物中心室内空气中的PM10、CO和CO2等进行了现场测定.结果表明,室内CO2和PM10浓度偏高.CO2全部超出了我国的室内空气标准,PM10全部超出了国家年平均标准,大部分超出了日平均标准.本文同时对购物中心内不同场所CO、CO2和PM10的浓度水平变化和来源特征进行了分析.     

Ambiental dust speciation and metal content variation in TSP, PM10 and PM2.5 in urban atmospheric air of Harare (Zimbabwe)

The effects of timber harvesting on stream water quality and efficiency of alternate streamside management zones were evaluated in Pockwock Lake and Five Mile Lake watersheds in central Nova Scotia, Canada. The streamside management zone (SMZ) included a 20 m no cut, 20 m select cut and a 30 m select cut buffer strips along the stream. Water quality of eight streams, six in harvested and two in not-harvested watersheds were monitored for two years before and two years after the harvesting of timber. Nonparametric statistical tests on stream water quality showed that there was significant change in the concentration of potassium in six streams, manganese in five streams, zinc in two streams and total nitrogen in one stream after timber harvesting. There was no significant change in the quality of water in two streams used as control sites in the neighboring watersheds of similar size and hydrological characteristics. The results show that forest management practices were most favorable in streams maintained with 30 m select cut followed by 20 m no cut and 20 m select cut SMZ. The streamside zone width and treatment of select cut or no cut in the zone played an important role in filtering or retaining the minerals in surface water runoff. In buffer zones of similar width, the buffer zone with no cut or forested buffer was relatively more effective at protecting stream water quality than select cut SMZ. The vegetation in the zone may have decreased the flow velocity and increased residence time and thus increased filtration and retention of minerals in the riparian soil.     

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

Air samples for PM(10) (dp?相似文献   

Evaluation of levels, sources and distribution of toxic elements in PM10 in a suburban industrial region, Rio de Janeiro, Brazil

The Oswaldo Cruz Foundation Campus (FIOCRUZ), in a suburban region of the city of Rio de Janeiro, was selected as a case study to assess the pollution released from vehicle and industrial facilities in Basin III, the most polluted area of the city. Concentrations of particulate matter (PM10) and trace metals in airborne particles were determined in an intensive field campaign. The samplings were performed every six days for 24 h periods, using a PM10 high volume sampler, from September 2004 to August 2005. PM10 mass concentrations were determined gravimetrically and the metals by ICP-OES. For PM10, the arithmetic mean for the period is 169 ± 42 μg m⁻³ which is 3.4 times the national recommended standard of 50 μg m⁻³. Additionally, 51% of the samplings exceeded the recommended 24 h limit of 150 μg m⁻³. Ca, Mg, Fe, Zn and Al were the metals that presented the higher concentrations. The correlation matrix gave two main clusters and three significant principal components (PC). Both PC1 and PC2 are associated to crustal, vehicular and industrial emissions while PC3 is mainly associated to geological material. Enrichment factors for Zn, Cu, Cd and Pb indicate that for these elements, anthropic sources prevail over natural inputs. PM10 levels showed a good correlation with hospital admissions for respiratory diseases in children and elderly people.     

Speciation and sources of atmospheric aerosols in a highly industrialised emerging mega-city in central China

Monitoring air quality in large urban agglomerations is the key to the prevention of air pollution-related problems in emerging mega-cities. The city of Wuhan is a highly industrialised city with >9 million inhabitants in Central China. Simultaneous PM10 sampling was performed during 1 year at one urban and one industrial site. Mean PM10 daily levels (156 microg m(-3) at the urban site and 197 microg m(-3) at the industrial hotspot) exceed the US-EPA or EU annual limit values by 3-4 times. A detailed study of daily speciation showed that the mean chemical composition of PM10 presents minimal differences between peak and low PM episodes. This implies that PM10 aerosols in the study area result from local emissions, and air quality management and abatement strategies in Wuhan should thus focus on local anthropogenic sources. The levels of some elements of environmental concern are relatively high (409-615 ngPb m(-3), 66-70 ngAs m(-3), 116-227 ngMn m(-3), 10-12 ngCd m(-3)) due to industrial, but also urban emissions. Principal component analysis identified a mineral source (probably cement and steel manufacture) and smelting as the main contributors to PM10 levels at the industrial site (34%), followed by a coal fired power plant (20%) and the anthropogenic regional background (16%). At the urban site the major PM10 source is a mixed coal combustion source (31%), followed by the anthropogenic regional background (28%) and traffic (16%).     

Chemical Elements and their Source Apportionment of PM10 in Beijing Urban Atmosphere

Ecological health in a temperate stream impacted by acid mine drainage (AMD) was evaluated by using a multimetric approach of the Index of Biological Integrity (IBI) based on natural fish assemblage. Recently, this approach has been widely used in many developed countries as a tool for ecological risk assessments of water environments. We used 10 metric systems, instead of 12 metrics suggested by Barbour, M. T., Gerritsen, J., Snyder, B. D., & Stribling, J. B. (1999). Rapid Bioassessment Protocols for Use in Streams and Wadeable Rivers: Periphyton, benthic Macroinvertebrates and Fish, 2nd edn. EPA 841-B-99-002. Washington, DC: U.S. Environmental Protection Agency, Office of Water, for a development of the regional IBI model, and used trophic guilds, habitat guilds, and richness variables for the calculation of IBI values. In the model, the attributes of four of 11 metrics were modified for the regional application. IBI values in the stream averaged 20.6 (n = 5), indicating a “poor condition” in terms of ecological health according to the modified criteria of U.S. EPA (1993). Fish Field and Laboratory Methods for Evaluating the Biological Integrity of Surface Waters. EPA 600-R-92-111. Environmental Monitoring systems Laboratory – Cincinnati office of Modeling, Monitoring systems, and quality assurance Office of Research Development, U.S. EPA, Cincinnati, Ohio, 45268. In particular, mean IBI values in the impacted areas of sites 2 and 3 were 13, and this health condition was categorized as “very poor condition.” IBI values in the impacted sites were significantly lower than the values found in the control. Also, we found that fishes in site sites 2 and 3 were not present during the study, and morphological deformity of Rhynchocypris oxycephalus was observed in site 4, influenced directly by sites 2 and 3, indicating a chemical impact in the sites. From the results of experiments in which AMD was treated with marine shells at stagnant condition, pH increased up to 6.0 from 3.1, and Fe and Al were removed up to 99% within 6 h. In the reactor experiment considering field application, pH of effluent maintained around 7.0. In addition, concentrations of Fe, Al, and heavy metals decreased remarkably in the effluents, and bottom-opened screen between neutralizer basins showed high effectiveness in the treatment of AMD.     

Characteristics and sources of atmospheric polycyclic aromatic hydrocarbons (PAHs) in Shanghai, China

A field campaign was conducted to measure and analyze 13 polycyclic aromatic hydrocarbons (PAHs) in six major zones in the city of Shanghai, P.R. China from August 2006 to April 2007. Ambient air samples were collected seasonally using passive air samplers, and gas chromatography–mass spectroscopy was used in this field campaign. The results showed that there was a sequence of 13 PAHs at Phen > FA > Pyr > Chr > Fl > An > BaA > BbFA > BghiP > IcdP > BkFA > BaP > DahA and the sum of these PAHs is 36.01 ± 10.85 ng/m³ in gas phase. FL, Phen, FA, Pyr, and Chr were the dominant PAHs in gas phase in the city. They contributed 90% of total PAHs in the gas phase. Proportion of measured PAHs with three, four, five, and six rings to total PAHs was 53%, 42%, 3%, and 2%, respectively. The highest concentration of ΣPAHs (the sum of 13 PAHs) occurred in the wintertime and the lowest was in the summer. This investigation suggested that traffic, wood combustion, and metal scrap burn emissions were dominant sources of the concentrations of PAHs in six city zones compared with coal burning and industry emissions. Further, the traffic emission sources of PAHs in the city were attributed mostly to gasoline-powered vehicles compared with diesel-powered vehicles. It was revealed that the seasonal changes in PAHs in the city depended on different source types. Metal scrap burn was found to be the major source of PAHs during the autumn, while the PAH levels in the atmosphere for winter and spring seasons were mainly influenced by wood and biomass combustion. Comparisons of PAHs among different city zones and with several other cities worldwide were also made and discussed.     

Distribution,sources, and toxicity assessment of polycyclic aromatic hydrocarbons in surface soils of a heavy industrial city,Liuzhou, China

As a heavy industrial city, Liuzhou has been facing a serious pollution problem. It is necessary to take steps to control and prevent environmental pollution wherever possible. Surface soil samples were collected from four communities in Liuzhou City, to determine the concentrations, distributions, sources, and toxicity potential of polycyclic aromatic hydrocarbons (PAHs) present. The mean concentrations of total PAHs in the surface soil are 756.43 ng/g for the heavy industrial area, 605.06 ng/g for the industrial area, 481.24 ng/g for the commercial–cum–residential area, and 49.93 ng/g for the rural area. Both the isomer ratio and principal component analyses for the PAHs prove that these pollutants originate mainly from coal, diesel, gasoline, and natural gas combustion. The pollution hierarchies and toxic equivalency factor of BaP prove that the city is subject to heavy pollution caused by industry, transportation, and daily human activities.     

宁波市PM10、PM2.5中水溶性无机阴离子浓度水平及分布特征

研究了宁波市PM10、PM2.5中无机阴离子浓度水平及分布特征。结果表明,PM10中Cl-为1.00μg/m3,具有较明显的海洋特征,SO24-、NO3-离子浓度为9.90、3.70μg/m3;Cl-主要存在于粒径为2.5-10μm的颗粒物中,而NO3-、SO42-主要存在于PM2.5中,成为PM2.5的重要组成部分。PM10中水溶性无机阴离子季节变化明显,呈冬天高,夏天低的趋势。     

Differences in the Spatial Distribution and Chemical Composition of PM10 Between the UK and Poland

The Fine Resolution Atmospheric Multi-pollutant Exchange Model was used to calculate the spatial distribution and chemical composition of PM₁₀ concentrations for two geographically remote countries in Europe—the UK and Poland—for the year 2007. These countries are diverse in terms of pollutant emissions as well as climate conditions. Information on the contribution of natural and anthropogenic as well as national and imported particles in total PM₁₀ concentrations in both countries is presented. The paper shows that the modelled national annual average PM₁₀ concentrations, calculated for the entire country area, are similar for the UK and Poland and close to 12 μg m^?3. Secondary inorganic aerosols dominate the total PM₁₀ concentrations in Poland. Primary particulate matter has the greatest contribution to total PM₁₀ in the UK, with large contribution of base cations. Anthropogenic sources predominate (81 %) in total PM₁₀ concentrations in Poland, whereas natural prevail in the UK—hence, the future reduction of PM₁₀ air concentrations by emissions reduction could be more difficult in the UK than in Poland.     

PM sources in a highly industrialised area in the process of implementing PM abatement technology. Quantification and evolution

Principal component analysis (PCA) coupled with a multilinear regression analysis (MLRA) was applied to PM(10) speciation data series (2002-2005) from four sampling sites in a highly industrialised area (ceramic production) in the process of implementing emission abatement technology. Five common factors with similar chemical profiles were identified at all the sites: mineral, regional background (influenced by the industrial estate located on the coast: an oil refinery and a power plant), sea spray, industrial 1 (manufacture and use of glaze components, including frit fusion) and road traffic. The contribution of the regional background differs slightly from site to site. The mineral factor, attributed to the sum of several sources (mainly the ceramic industry, but also with minor contributions from soil resuspension and African dust outbreaks) contributes between 9 and 11 microg m(-3) at all the sites. Source industrial 1 entails an increase in PM(10) levels between 4 and 5 microg m(-3) at the urban sites and 2 microg m(-3) at the suburban background site. However, after 2004, this source contributed less than 2 microg m(-3) at most sites, whereas the remaining sources did not show an upward or downward trend along the study period. This gradual decrease in the contribution of source industrial 1 coincides with the implementation of PM abatement technology in the frit fusion kilns of the area. This relationship enables us to assess the efficiency of the implementation of environmental technologies in terms of their impact on air quality.     

北京清华园采暖前与采暖期PM10中含碳组分的理化特征

采用美国rp公司生产的Series5400大气颗粒物碳质组分监测仪对清华园PM10中的碳质组分进行了连续在线监测(2002年9月~11月)。结合PM2.5中碳质组分浓度、PM10的浓度和气象数据,分析了碳质组分的污染特征。结果表明,采样期间清华园大气PM10中有机碳(OC)、元素碳(EC)的日平均质量浓度分别在4.07~65.81μg/m3、0.96~26.14μg/m3之间变化,平均值分别为20.8±12.1和7.0±5.1μg/m3。OC在总碳(TC)中占有很大比例,OC/TC平均值为75.84%;TC在PM10中的含量平均为25.0%。本文对9~10月份(秋季)和11月份(初冬)OC、EC的相关性分别进行了分析,结果表明OC、EC之间具有良好的相关性,9月份和10月份相关性系数(R2)为0.83;11月份为0.90。二次生成的OC(OCsec)浓度估算结果表明,9、10月份OCsec在OC中的比例(60.7%)比11月份(38.5%)大。碳质组分主要集中在细颗粒物中,PM10中的OC有70.3%存在于细颗粒物PM2.5中,TC则有58.6%存在于PM2.5中。