Study on particulate and metallic elements variation at daytime and nighttime period in urban atmosphere

Daily PM_2.5, PM_2.5–10 and TSP have been collected by Universal and PS‐1 sampler simultaneously at a site within Taichung between February and March 1999. The filters were analyzed by atomic absorption spectrophotometry for the elemental analysis of Ca, Fe, Mn, Pb, Cu, Zn and Cr. In general, the concentration of these metallic elements are higher in fine particles than in coarse particles. On average, PM₁₀ accounted for 67% of the TSP at daytime, while at nighttime PM₁₀ accounted for only 44% of the TSP. For PM_2.5, PM₂._5–10 and TSP concentrations, there were no significant differences between day and night period. The averaged concentrations of metallic elements in PM_2.5 at daytime were all higher than that at nighttime. Ca, Fe and Zn have large and variable PM_2.5 concentrations at both daytime and nighttime. For the daytime Zn and Pb account for the largest portion of the heavy metal elements. For the nighttime, Zn and Cr make the largest portion of the heavy metal elements. The concentrations of Mn were higher on fine particulates. The trace metals Cu and Cr in Taichung are probably due to particulates emitted by Taichung Fire Power Plants transported into the sampling area by the prevailing northwesterly wind.     

PIXE characterization of PM10 and PM2.5 particulates sizes collected in Ikoyi Lagos,Nigeria

Ambient concentrations of PM₁₀ (x?≤?10?µm) and PM_2.5 (x?≤?2.5?µm) particulate fractions collected from Ikoyi Lagos, Nigeria, as well as their elemental compositions are presented in this study. Both size-segregated fractions were collected using a double staged ‘Gent’ stack filter unit sampler. Elemental characterizations of dust laden filters were carried out using proton-induced X-ray emission (PIXE) technique. Twenty-two elements (Si, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Pb, Br, Rb, Sr, Zr, Ag, Cd, and Ta) were detected as well as their concentrations and correlations were determined for both particulate size fractions. Their correlation matrix result indicates that some of the trace elements detected could have common source origins or similar chemical properties. The results were similar to the levels observed in moderately polluted urban areas and there is need for source identification and apportionment using receptor models in future studies.     

Ambient air particulates-bound metallic elements sources identifications during winter and summer at a Science Park

The ambient air particulates pollutants of total suspended particulates (TSP) and PM_2.5 were collected by using PS-1 and Wilbur PM_2.5 sampler, simultaneously during the year of 2015–2017 at a photoelectric factory in Science Park of central Taiwan. And those of the ambient air atmospheric metallic elements (Cr, Mn, Ni, Cu, Zn, Pb) concentrations which attached on the TSP and PM_2.5 were analyzed by using inductively coupled plasma optical emission spectrometer. In addition, identifying anthropogenic and natural pollutants sources were conducted by using the enrichment factor (EF) and principal component analysis (PCA) methods. The results indicated that the average TSP and PM_2.5 concentrations were ranked highest in winter season, while summer season was ranked lowest during the year of 2015–2016. In addition, the average highest metallic element concentrations were occurred in winter season for both TSP and PM_2.5 during the year of 2015–2016, while the average lowest metallic elements concentrations in TSP and PM_2.5 were also occurred in winter season during the year of 2016–2017. Moreover, the EF analysis results showed that the metallic element Zn came from anthropogenic emission source. As for metallic element Mn, the results showed that metallic element Mn was mainly attributed to natural emission in this study. Finally, the PCA results showed that metallic elements Cr, Zn and Pb were the dominant emissions metallic elements in this study. As for PM_2.5, the results showed that the metallic elements Cr, Cu and Pb were the dominant emissions metallic elements at this HPB sampling site.

     

PM<Subscript>2.5</Subscript> particulates and metallic elements (Ni,Cu, Zn,Cd and Pb) study in a mixed area of summer season in Shalu,Taiwan

PM_2.5 has become an important environmental issue in Taiwan during the past few years. Moreover, electricity increased significantly during the summertime and TTPP generated by coal burning base is the main electricity provider in central Taiwan. Therefore, summer season has become the main research target in this study. The ambient air concentrations of particulate matter PM_2.5 and PM₁₀ collected by using VAPS at a mixed characteristic sampling site were studied in central Taiwan. The results indicated that the average daytime PM_2.5 and PM₁₀ particulate concentrations were occurred in May and they were 44.75 and 57.77 µg/m³ in this study. The results also indicated that the average nighttime PM_2.5 and PM₁₀ particulate concentrations were occurred in June and they were 38.19 and 45.79 µg/m³ in this study. The average PM_2.5/PM₁₀ ratios were 0.7 for daytime, nighttime and 24-h sampling periods in the summer for this study. This value was ranked as the lowest ratios when compared to the other seasons in previous study. Noteworthy, the results further indicated that the metallic element Pb has the mean highest concentrations for 24-h, daytime and nighttime sampling periods when compared to those of the other metallic elements (Ni, Cu, Zn and Cd). The average mean highest metallic Pb concentrations in PM10 were 110.7, 203.0 and 207.2 ng/m³ for 24-h, daytime and nighttime sampling periods in this study. And there were 59.53, 105.2 and 106.6 ng/m³ for Pb in PM2.5 for 24-h, daytime and nighttime sampling periods, respectively. Moreover, the results further indicated that mean metallic element Pb concentrations on PM_2.5 and PM₁₀ were all higher than those of the other elements for 24 h, day and nighttime.     

Atmospheric particulate matter in Nigerian megacities

The paucity of data on air pollution indices in Nigeria prompted us to commence a national screening exercise regarding particulate matter loads. Six potential megacities (Aba, Abuja, Lagos, Kano, Maiduguri, and Port-Harcourt) representing the six geographical zones in Nigeria were chosen for the study. Sampling was achieved using a ‘Gent’ stacked filter unit sampler capable of collecting fractions of particulate matter with sizes of <10-μm and <2.5-μm simultaneously. The mean values for PM₁₀ are 550, 35, 87, 340, 246 and 130 μg m^?3 while for PM_2.5 the mean values are 100, 14, 25, 67, 20 and 30 μg m^?3 respectively for Aba, Abuja, Lagos, Kano, Maiduguri, and Port-Harcourt. Except for Abuja, the daily PM₁₀ mass loads exceeded the World Health Organization (WHO) guidelines daily limit where as the PM_2.5 values were within the WHO guideline limit. Their correlation matrix result indicates that some PM_2.5 fractions mass fractions were strongly correlated than the PM₁₀ fractions probably due to their long range transport potentials. Further work is in progress to determine the elemental profiles of both particulate fractions collected.     

The pollution characteristics of PM<Subscript>2.5</Subscript> and correlation analysis with meteorological parameters in Xinxiang during the Shanghai Cooperation Organization Prime Ministers’ Meeting

The pollution characteristics of PM_2.5 and correlation analysis with meteorological parameters in Xinxiang during the Shanghai Cooperation Organization Prime Ministers’ Meeting were investigated. During the whole meeting, nine PM_2.5 samples were collected at a suburban site of Xinxiang, and the average concentration of PM_2.5 was 122.28 μg m^?3. NO₃ ^?, NH₄ ⁺, SO₄ ^2? accounted for 56.8% of the total water-soluble ions. In addition, with an exception of Cl^?, all of water-soluble ions decreased during the meeting. Total concentrations of crustal elements ranged from 6.53 to 185.86 μg m^?3, with an average concentration of 52.51 μg m^?3, which accounted for 82.5% of total elements. The concentrations of organic carbon and elemental carbon were 7.71 and 1.52 μg m^?3, respectively, lower than those before and after the meeting. It is indicated that during the meeting, limiting motor vehicles is to reduce exhaust emissions, delay heating is to reduce the fossil fuel combustion, and other measures are to reduce the concentration of PM_2.5. The directly dispersing by mixing layerheight increase and the indirectly reducing the formation of secondary aerosol by low relative humidity, andthese are the only two key removing mechanisms of PM_2.5 in Xinxiang during the meeting.     

Water-soluble inorganic ions in airborne particulates from the nano to coarse mode: a case study of aerosol episodes in southern region of Taiwan

In 2004, airborne particulate matter (PM) was collected for several aerosol episodes occurring in the southern region of Taiwan. The particulate samples were taken using both a MOUDI (Micro-orifice Uniform Deposit Impactor) and a nano-MOUDI sampler. These particulate samples were analyzed for major water-soluble ionic species with an emphasis to characterize the mass concentrations and distributions of these ions in the ambient ultrafine (PM_0.1, diameter <0.1 μm) and nano mode (PM_nano, diameter <0.056 μm) particles. Particles collected at the sampling site (the Da-Liao station) on the whole exhibited a typical tri-modal size distribution on mass concentration. The mass concentration ratios of PM_nano/PM_2.5, PM_0.1/PM_2.5, and PM₁/PM_2.5 on average were 1.8, 2.9, and 71.0%, respectively. The peak mass concentration appeared in the submicron particle mode (0.1 μm < diameter <1.0 μm). Mass fractions (percentages) of the three major water-soluble ions (nitrate, sulfate, and ammonium) as a group in PM_nano, PM_0.1, PM₁, and PM_2.5 were 18.4, 21.7, 50.0, and 50.7%, respectively. Overall, results from this study supported the notion that secondary aerosols played a significant role in the formation of ambient submicron particulates (PM_0.1−1). Particles smaller than 0.1 μm were essentially basic, whereas those greater than 2.5 μm were neutral or slightly acidic. The neutralization ratio (NR) was close to unity for airborne particles with diameters ranging from 0.18 to 1 μm. The NRs of these airborne particles were found strongly correlated with their sizes, at least for samples taken during the aerosol episodes under study. Insofar as this study is exploratory in nature, as only a small number of particulate samples were used, there appears to be a need for further research into the chemical composition, source contribution, and formation of the nano and ultrafine mode airborne particulates.     

Modelling concentrations of airborne primary and secondary PM10 and PM2.5 with the BelEUROS-model in Belgium

The Eulerian Chemistry-Transport Model BelEUROS was used to calculate the concentrations of airborne PM₁₀ and PM_2.5 over Europe. Both primary as well as secondary particulate matter in the respirable size-range was taken into account. Especially PM_2.5 aerosols are often formed in the atmosphere from gaseous precursor compounds. Comprehensive computer codes for the calculation of gas phase chemical reactions and thermodynamic equilibria between compounds in the gas-phase and the particulate phase had been implemented into the BelEUROS-model. Calculated concentrations of PM₁₀ and PM_2.5 are compared to observations, including both the spatial and daily, temporal distribution of particulate matter in Belgium for certain monitoring locations and periods. The concentrations of the secondary compounds ammonium, nitrate and sulfate have also been compared to observed values. BelEUROS was found to reproduce the observed concentrations rather well. The model was applied to assess the contribution of emissions derived from the sector agriculture in Flanders, the northern part of Belgium, to PM₁₀- and PM_2.5-concentrations. The results demonstrate the importance of ammonia emissions in the formation of secondary particulate matter. Hence, future European emission abatement policy should consider more the role of ammonia in the formation of secondary particles.     

Review of total suspended particles (TSP) and PM<Subscript>2.5</Subscript> concentration variations in Asia during the years of 1998–2015

In Asian countries such as China, Malaysia, Pakistan, India, Taiwan, Korea, Japan and Hong Kong, ambient air total suspended particulates and PM_2.5 concentration data were collected and discussed during the years of 1998–2015 in this study. The aim of the present study was to (1) investigate and collect ambient air total suspended particulates (TSP) and PM_2.5 concentrations for Asian countries during the past two decades. (2) Discuss, analyze and compare those particulates (TSP and PM_2.5) annual concentration distribution trends among those Asian countries during the past two decades. (3) Test the mean concentration differences in TSP and PM_2.5 among the Asian countries during the past decades. The results indicated that the mean TSP concentration order was shown as China > Malaysia > Pakistan > India > Taiwan > Korea > Japan. In addition, the mean PM_2.5 concentration order was shown as Vietnam > India > China > Hong Kong > Mongolia > Korea > Taiwan > Japan and the average percentages of PM_2.5 concentrations for Taiwan, China, Japan, Korea, Hong Kong, Mongolia and Other (India and Vietnam) were 8, 21, 6, 8, 14, 13 and 30%, respectively, during the past two decades. Moreover, t test results revealed that there were significant mean TSP and PM_2.5 concentration differences for either China or India to any of the countries such as Taiwan, Korea and Japan in Asia during the past two decades for this study. Noteworthy, China and India are both occupied more than 60% of the TSP and PM_2.5 particulates concentrations out of all the Asia countries. As for Taiwan, the average PM_2.5 concentration displayed increasing trend in the years of 1998–1999. However, it showed decreasing trend in the years of 2000–2010. As for Korea, the average PM_2.5 concentrations showed decreasing trend during the years of 2001–2013. Finally, the average PM_2.5 concentrations for Mongolia displayed increasing trend in the years of 2004–2013.     

Airborne fine particulate matter (PM2.5) at industrial,high- and low-density residential sites in a Nigerian megacity

Abstract

Airborne particulate matter PM_2.5 was collected in an industrial, a low-density, and a high-density residential area of Lagos from December 2010 to November 2011, and elemental composition was determined by proton-induced X-ray emission. Across the months, mass concentrations ranged from 13 to 237?µg?m^?3, exceeding the World Health Organization guideline value of 10?µg?m^?3. Data on 24 elements were obtained, with maximum values during Harmattan season months; source identification and apportionment studies by positive matrix factorization suggested that petroleum oil combustion (70%) was the major source of PM_2.5 and could pose a great hazard to Lagos receptors.     

Characterization of chemical species in universal sampler (PM2.5 and PM2.5–10) aerosols in suburban area of central Taiwan

Aerosol samples of particulate and chemical species for PM₁₀ (particulate matter with aerodynamic diameters less than 10 μm) collected by Universal sampler were studied from June to August 1998 in the suburban area of central Taiwan. The ratios of PM_2.5/PM_2.5–10 displayed that the fine particles (particle size < 2.5 μm) are prevailing in the suburban site. Ion Chromatography was used to analyze for the water‐soluble ions: sulphate and nitrate in the Universal samples. Also, the collected samples were analyzed by atomic absorption spectrophotometry for the elemental analysis of Ca, Fe, Pb, Cu and Cr. The results indicated that the crustal elements (Ca and Fe) and resuspended matters were dominated in the coarse particulate mode while the anthropogenic elements (Cr, Pb, Cu) and sulphate components are mainly in the fine particle fraction. The results also showed that the sulphate and nitrate make the largest portion of the chemical species collected by Universal sampler (PMio). The concentrations of heavy metals in THU are generally high, owing to the higher motor vehicle and industrial density nearby. The degree of pollution from this source differs from day to day, depending on the motor vehicle density.     

Characteristics,sources and health risk assessment of toxic heavy metals in PM<Subscript>2.5</Subscript> at a megacity of southwest China

Twenty trace elements in fine particulate matters (i.e., PM_2.5) at urban Chengdu, a southwest megacity of China, were determined to study the characteristics, sources and human health risk of particulate toxic heavy metals. This work mainly focused on eight toxic heavy metal elements (As, Cd, Cr, Cu, Mn, Ni, Pb and Zn). The average concentration of PM_2.5 was 165.1 ± 84.7 µg m^?3 during the study period, significantly exceeding the National Ambient Air Quality Standard (35 µg m^?3 in annual average). The particulate heavy metal pollution was very serious in which Cd and As concentrations in PM_2.5 significantly surpassed the WHO standard. The enrichment factor values of heavy metals were typically higher than 10, suggesting that they were mainly influenced by anthropogenic sources. More specifically, the Cr, Mn and Ni were slightly enriched, Cu was highly enriched, while As, Cd, Pb and Zn were severely enriched. The results of correlation analysis showed that Cd may come from metallurgy and mechanical manufacturing emissions, and the other metals were predominately influenced by traffic emissions and coal combustion. The results of health risk assessment indicated that As, Mn and Cd would pose a significant non-carcinogenic health risk to both children and adults, while Cr would cause carcinogenic risk. Other toxic heavy metals were within a safe level.     

贵阳市冬季PM_(2.5)中典型重金属元素的化学形态分析与健康风险评价

为了更准确地研究重金属的生物有效性和对环境与人体的潜在生态危害,采用改进BCR法分析了贵阳市冬季PM_(2.5)中Cu、Mn、Co、Cd、Pb这5种重金属元素的化学形态,并评价了它们的生物有效性和健康风险。结果表明:不同重金属元素形态分布存在差异,Cu主要是弱酸溶态,其次是可氧化态;Mn主要是弱酸溶态,其次是残渣态;Co没有检测出可还原态,而在其他3种形态分布比较平均;Pb和Cd绝大部分都是弱酸溶态。生物有效性系数(K)分析结果表明:重金属生物有效性强弱顺序为CdPbMnCuCo,其中Cd和Pb的K0.8,属于生物可利用性元素;Mn、Cu、Co的K值在0.4~0.7之间,属于潜在生物可利用性元素。健康风险评价表明:成人的致癌风险比儿童大,尤其Cd对成年人存在潜在的致癌风险,且成年男性高于成年女性;Mn存在潜在非致癌风险,且对儿童的风险最大。     

Characterization and distribution of mineral content in fine and coarse airborne particle fractions by neutron activation analysis∗

Nowadays, much attention is devoted to the study of toxic elements at trace and sub-trace levels in the investigation of particulate matter composition, especially in PM₁₀ and PM_2.5. Furthermore, it should be considered that the behavior knowledge is an other important task for understanding such species. Finally, the determination of particular elements with a few data in literature can assume relevant importance in industrial processes (Pd, Rh, Ir, etc. for catalytic pot, Sm, Ce, Eu, etc. for optical fibers and electronic process). In this article, we apply a nuclear technique, i.e. Instrumental Neutron Activation Analysis, for the study of metal composition in fine and coarse fractions. This nuclear technique allows the determination of about 25 elements: for some of them, this is the first determination in the ambient air of Rome. The investigation was performed in a reserved area in downtown Rome during a 15-day intensive campaign. The sampled filters were irradiated at the nuclear reactor Triga Mark II (ENEA-Casaccia Laboratories) at neutron flux of 2.6?×?10¹²?n?cm^?2?s^?1 for 32.55?h. The measurements of the γ-ray allow the qualitative and quantitative analysis. The element levels in fine and coarse fractions will be shown with the correlations among some elements being more interesting in the toxicological field: basically, the concentrations are very low.     

Mitochondrial toxicity and in vitro biological effects of ambient PM2.5 from an urban site in China

Abstract

The roles of PM_2.5-induced mitochondrial damage and oxidative stress on mast cell degranulation were examined in vitro. Mast cells were treated with suspensions of PM_2.5 in Dulbecco’s modified Eagle’s medium at concentrations from 25 to 200?mg/L in the absence or presence of 10?mmol/L N-acetyl-L-cysteine. Biological effects and mitochondrial function were assessed by determining cell viability, β-hexosaminidase release, interleukin-4 secretion, reactive oxygen species generation, adenosine triphosphate production, potential alteration of mitochondrial membrane, and activities of mitochondrial electron transport chain complexes I and III. Exposure of mast cells to PM_2.5 induced reduction of adenosine triphosphate production, collapse of mitochondrial membrane potential, and inhibition of the activity of complex III. Co-treatment of mast cells exposed to PM_2.5 with N-acetyl-L-cysteine attenuated cytotoxicity and the production of reactive oxygen species, and decreased the release of β-hexosaminidase and interleukin-4. Evidently, PM_2.5-induced oxidative stress plays an essential role in mitochondrial toxicity and mast cell activation.     

High reduction of ozone and particulate matter during the 2016 G-20 summit in Hangzhou by forced emission controls of industry and traffic

Many regions in China experience air pollution episodes because of the rapid urbanization and industrialization over the past decades. Here we analyzed the effect of emission controls implemented during the G-20 2016 Hangzhou summit on air quality. Emission controls included a forced closure of highly polluting industries, and limiting traffic and construction emissions in the cities and surroundings. Particles with aerodynamic diameter lower than 2.5 μm (PM_2.5) and ozone (O₃) were measured. We also simulated air quality using a forecast system consisting of the two-way coupled Weather Research and Forecast and Community Multi-scale Air Quality (WRF-CMAQ) model. Results show PM_2.5 and ozone levels in Hangzhou during the G-20 Summit were considerably lower than previous to the G-20 Summit. The predicted concentrations of ozone were reduced by 25.4%, whereas the predicted concentrations of PM_2.5 were reduced by 56%.     

电镀企业周边大气颗粒物PM_(2.5)、PM_(10)和TSP中重金属分布特征及健康风险评价

以东莞市5个镇区为研究对象,采集电镀企业周边大气样品,分析了样品中重金属(包括As、Co、Cd、Cr、Cu、Mn、Ni、Pb、Sb、V、Zn和Hg)的含量分布,使用富集因子(enrich factor)、地累积指数(index of geoaccumulation)、Hakanson法和美国国家环境保护局(US EPA)的人体暴露健康风险评价模型,对PM_(2.5)、PM_(10)、总悬浮颗粒物(TSP)中重金属进行人体健康风险评价。结果表明,PM_(2.5)、PM_(10)和TSP中As、Cd和Cr平均浓度皆超标。Cr、Ni和V元素在3种颗粒物中非富集,主要为自然源;As、Co、Cu、Pb和Zn,可能来源于自然源和叠加的工业污染。Cd、Hg和Sb浓度受人为污染影响严重。Cd、Sb、Cu、Zn、Pb为生物可利用元素(K>0.6),在环境中的可迁移性高且易于被生物体和人体吸收。Mn元素的非致癌风险值较其他重金属要高1~4个数量级,且儿童的非致癌暴露风险值HQ均高于成人的。3种颗粒物中重金属元素通过呼吸吸入途径产生的非致癌风险HI值均高于人体可接受的上限1.0,其主要贡献来源于Mn的影响,研究区非致癌风险较为严重。除PM_(10)中Co元素和TSP中Co、Cr的成人致癌风险CR值大于10-4之外,其余大部分重金属元素通过呼吸途径产生的致癌风险CR值均在可接受范围之内,此外,3种颗粒物中的成人的致癌暴露风险值CRT均高于儿童的CRT值,并且除了PM_(2.5)中儿童的重金属致癌暴露风险CRT值(4.70E-05)低于人体可接受范围的上限(10-4),其余CRT值均高于10-4,致癌风险较为严重。     

Particle size distributions, PM2.5 concentrations and water-soluble inorganic ions in different public indoor environments: a case study in Jinan, China

In this study, we collected particles with aerodynamic diameter ?2.5 μm (PM_2.5) from three different public indoor places (a supermarket, a commercial office, and a university dining hall) in Jinan, a medium-sized city located in northern China. Water-soluble inorganic ions of PM_2.5 and particle size distributions were also measured. Both indoor and outdoor PM_2.5 levels (102.3–143.8 μg·m^?3 and 160.2–301.3 μg·m^?3, respectively) were substantially higher than the value recommended by the World Health Organization (25 μg·m^?3), and outdoor sources were found to be the major contributors to indoor pollutants. Diurnal particle number size distributions were different, while the maximum volume concentrations all appeared to be approximately 300 nm in the three indoor locations. Concentrations of indoor and outdoor PM_2.5 were shown to exhibit the same variation trends for the supermarket and dining hall. For the office, PM_2.5 concentrations during nighttime were observed to decrease sharply. Among others, SO ₄ ^2? , NH ₄ ⁺ and NO ₃ ^? were found to be the dominant water-soluble ions of both indoor and outdoor particles. Concentrations of NO ₃ ^? in the supermarket and office during the daytime were observed to decrease sharply, which might be attributed to the fact that the indoor temperature was much higher than the outdoor temperature. In addition, domestic activities such as cleaning, water usage, cooking, and smoking also played roles in degraded indoor air quality. However, the results obtained here might be negatively impacted by the small number of samples and short sampling durations.     

Cluster analysis of inorganic elements in particulate matter in the air environment of an equatorial urban coastal location

Concentrations of nine inorganic elements (Na, Zn, Ca, Fe, Ni, Mn, Cu, Cd and Al) in particulate matter (PM₁₀) in the air of an equatorial urban coastal location during 2009 were studied during summer and winter monsoon seasons using high-volume sampling techniques. Atomic absorption spectrophotometry was used to analyse the samples. The concentrations of most inorganic elements were higher during summer than winter, except for Cu and Zn. The main inorganic elements in PM₁₀ are Na, Zn and Ca. High concentrations of Na and Ca are due to marine aerosols. Analysis of enrichment factors showed that inorganic elements are from non-crustal sources. Cluster analysis identified five clusters in the summer and six in the winter: (1) PM₁₀–Ni, (2) Zn–Na, (3) Fe–Cu–Ca–Cd, (4) Mn and (5) Al for summer; and (1) PM₁₀, (2) Zn, (3) Fe–Ni, (4) Cu–Ca–Na–Cd, (5) Mn and (6) Al for winter. Combining both correlation and cluster analysis, it was found that Fe–Cu–Cd was from industry/vehicle emissions, Zn was from resuspended soil, Mn was from metallurgical processes, Ni was from a nearby power plant and Al was from crustal sources. Inorganic element concentrations could be a good indicator of local sources of PM₁₀.     

Observation of black carbon aerosol in Beijing, 2003

The objective of this study was to determine the black carbon concentration in Beijing in 2003. The aerosol properties were measured using an Aethalometer and a tapered element oscillating microbalance (TEOM) on the roof of the Physics Building of Peking University (39.99° N, 116.31° E) from July to August 2003 and from November 2003 to January 2004. The average black carbon (BC) concentrations in the summer and winter were 8.80 and 11.4 μg/m³, respectively. During winter, two different cyclone cut offs were installed at the inlet of an aethalometer. The BC mass concentration in TSP, PM₁₀, and PM_2.5 were obtained. The results indicated that in winter aerosol, 90% of BC exited in PM₁₀ and 82.6% of BC exited in PM_2.5. The BC in PM₁₀ accounted for 5.11% of the PM₁₀ mass.