Exploring data quality for some inorganic and organic constituents of inhalable particulate matter (PM10)

Quality assurance (QA) assessments of air pollution data sets provide a basis for evaluating the significance of various substances in the atmosphere. For non-criteria pollutants, QA results are seldom reported in the technical literature and are often difficult to estimate. The present report provides a summary of QA results such as recovery, precision and accuracy data. Of the six trace elements and nine organic constituents compared in detail, recoveries, laboratory precision and laboratory accuracy values were 100%, ±3% to ±19% and-2 to-13% for the former group and 69% to 98%, ±7% to 23% and-15 to-34% for the later group. System precision varied from ±22% to ±47% for the trace elements and ±42% to ±83% for the organic constituents. Limitations in the interpretation of non-criteria particulate-phase pollutant data bases are discussed with some emphasis placed on receptor-modelling and risk assessment applications. Finally, the relevance of NBS certified materials for QA estimates in non-criteria air pollutant studies is also reviewed.     

Carbon speciation in airborne particulate matter with C (1s) NEXAFS spectroscopy

Recent and current research activities on the chemical characterization of carbon in airborne carbonaceous particulate matter with near-edge X-ray absorption fine structure (NEXAFS) spectroscopy are reviewed. NEXAFS spectroscopy uses soft X-rays from synchrotron radiation facilities and allows for the bulk and surface speciation of particulates smaller than 2.5 micrometres (PM 2.5). This relatively novel technique is often superior to TEM-EELS and FTIR spectroscopy. In the extreme case, one single PM particle is sufficient for characterization. Liquids, extracts, solid core and surface functional groups can be quantified. Preliminary data on combustion derived PM such as diesel soot, wood smoke and tobacco smoke are compared with ambient samples.     

Analysis of crystalline phases in airborne particulate matter by two-dimensional X-ray diffraction (XRD2)

In this work, the potentiality of two-dimensional X-ray diffraction (XRD(2)) to characterise aerosol particles collected on commercial glass filters is presented. Indeed, even if routine analysis usually requires only mass determination, and rarely chemical composition, phase determination is fundamental to recognize the primary or secondary origin of the particulate matter and thus to determine the main sources of the pollution and to model contamination events. The experiments were performed at Daresbury Synchrotron (UK) Laboratory on 14.1 Beamline. The analysis of filters collected in Tuscany (Italy) is discussed with particular attention to the presence of arsenic sulfide. The first results of these experiments are very promising, showing the presence of unexpected compounds in the particulate matter of the investigated area.     

Concentrations, sources, and exposure profiles of polycyclic aromatic hydrocarbons (PAHs) in particulate matter (PM10) in the north central part of India

Airborne particulates (PM₁₀) from four different areas within Agra city (a semi-arid region) were collected using respirable dust samplers during the winter season (Nov. 2005–Feb 2006) and were then extracted with methylene chloride using an automated Soxhlet Extraction System (Soxtherm^®). The extracts were analyzed for 17 target polycyclic aromatic hydrocarbons (PAHs) and the heterocycle carbazole. The average concentration of total PAH (TPAH) ranged from 8.04 to 97.93 ng m^???3. The industrial site had the highest TPAH concentration followed by the residential, roadside, and agricultural sites. Indeno(1,2,3-cd)pyrene, benzo(g,h,i)perylene, and benzo(b)fluoranthene were the predominant compounds found in the samples collected from all of the sites. The average B(a)P-equivalent exposure, calculated by using toxic equivalent factors derived from literature and the USEPA, was approximately 7.6 ng m^???3. Source identification using factor analysis identified prominent three, four, four, and four probable factors at industrial, residential, roadside, and agricultural sites, respectively.     

Size Distribution of Aerosols (PM10) and Lead (Pb) near Traffic Intersections in Mumbai (India)

The size distribution of aerosols was measured near traffic intersections of Marol link road in air quality control region (AQCR1), which is a moderately industrial area and Dadar Khodad circle in AQCR2, which is a heavily commercial core of the Mumbai City. The reason behind selecting the two unidentical regions was to study the contribution from vehicles to the size separated PM10 and that of Pb. It is recognised that particulates in urban air are responsible for serious health effects. As very small particles are assumed to be important for the adverse health effects, the particle size distribution is thus an important factor that needs to be addressed whenever the particulates pollution is concerned. The size measurements were done with a cascade impactor of eight stages with a back-up filter. It effectively separates the particulate matter into nine-sizes ranging from 0.0-0.4 to 9.0-10.0 microm. Samples were analysed in nine-particle size fractions with special reference to a toxic metal - lead (Pb) by atomic absorption spectrophotometry (AAS). It was found that PM10 and Pb at both the intersections could easily be classified by the size distribution. The fractions of the PM10 and that of Pb showing a tendency of trimodal distributions with the first peak at coarse mode approximately 9.0-10.0 microm, second at approximately 5.8 microm and the third at coarse mode approximately1.1 microm. The significant percentage of Pb was found in the range below 2.5 microm at both the intersections. However, Pb in AQCR1 is found in the coarser range as well, which could probably be the influence of various industrial activities in the area. PM10 concentration values in the coarser range in AQCR2 are associated with the resuspension of dust particles and mechanical erosions.     

Human health damage caused by particulate matter PM10 and ozone in urban environments: the case of Athens, Greece

Studies conducted over the past decades have provided substantial evidence that both the long- and the short-term exposures to ozone and particulate matter are responsible for mortality and cardiopulmonary morbidity. This paper examines the relationship between exposure to ambient concentrations of ozone (O₃) and particulate matter with aerodynamic diameter of less than 10 μm (PM₁₀) and public health and provides the quantification of the burden of disease from PM₁₀ and O₃-related mortality and morbidity through a Life Cycle Impact Assessment focused on the greater area of Athens, Greece. Thus, characterizations factors (CFs) for human health damage are calculated in 17 sites in Athens, in terms of the annual marginal change in the disability-adjusted life years (DALYs) due to a marginal increase in the ambient concentrations. It is found that the PM₁₀ intake factors range between 1.25?×?10^?6 and 2.78?×?10^?6, suggesting that 1.25–2.78 μg of PM₁₀ are inhaled by the Athenian population per kg of PM₁₀ in the urban atmosphere. Mortality due to chronic exposure to PM₁₀ has a dominant contribution to years of life lost with values ranging between 6.2?×?10^?5 and 1.1?×?10^?4. On the other hand, the mortality caused by short-term exposure to O₃ is weaker with the CFs ranging between 1.58?×?10^?7?years of life lost in the urban/traffic areas and 4.71?×?10^?7?years in the suburbs. Finally, it is found that 9,000 DALYs are lost on average in Athens, corresponding to 0.0018 DALYs per person. This is equal to 0.135 DALYs per person over a lifetime of approximately 75 years, assuming constant emission rates for the whole period.     

Fractionation of eleven elements by chemical bonding from airborne particulate matter collected in an industrial city in Argentina

A four-step chemical sequential extraction procedure was used to evaluate the distribution of Al, As, Cr, Cu, Fe, Mn, Ni, Pb, Ti, V and Zn in airborne particulate matter collected on glass fibre filters using a high-volume sampler. Two sets of samples were collected in 2001 (winter and summer campaigns) in representative zones of an industrial city of Argentina. The leaching scheme was applied to PM-10 particles and consisted in extracting the elements in four fractions, namely soluble and exchangeable elements; carbonates, oxides and reducible elements; bound to organic matter and sulfidic metals; and residual elements. Metals and metalloids at microg g(-1) level were determined in each fraction by inductively coupled plasma optical emission spectrometry (ICP OES). Analyte concentration varied from 14 microg g(-1) (equivalent to 1.0 ng m(-3)) for As to 11.8 mg g(-1) (equivalent to 2,089 ng m(-3)) for Al. Seven elements, namely Al, Cr, Fe, Mn, Pb, Ti and Zn showed similar distributions in both seasons while As was distributed in a significantly different manner in each season. The results exhibited low As contents in the first and second fractions that could be associated with routine coal combustion and a high content in the third and fourth fractions of the summer samples that could be linked to the use of pesticides. Aluminium, As, Cu, Mn, Ni, Ti, V and Zn were found in different percentages in the more bioavailable aqueous fraction with As, Mn, V and Zn exhibiting solubilities greater than 1% while Cr and Pb being insoluble. The content of Al, Cr, Cu, Fe, Ni, Pb, and Zn in the residual fraction was, in average, higher than 50%. A comparative assessment of the use of the underlying information available from fractionation studies compared to that obtained from total element content was done for Fe and Mn. It showed that the results obtained using chemical sequential extraction procedures allowed further discrimination of the potential air pollution sources.     

Acidic and basic properties and buffer capacity of airborne particulate matter in an urban area of Beijing

Particles with aerodynamic diameters <10  $\upmu $ m (PM₁₀) and particles with aerodynamic diameters <2.5  $\upmu $ m (PM_2.5) were sampled during summer 2006 in Beijing and mass concentrations, water-soluble ionic compounds concentrations, and acidic buffer capacity were analyzed. Results show that the mass concentration ranges of PM₁₀ and PM_2.5 were from 56.4 to 226.6  $\upmu $ g/m³ and from 31.3 to 200.7  $\upmu $ g/m³ during sampling days, respectively. Concentrations of F^???, Cl^???, NO $_{3}^{\,\,-}$ , NO $_{2}^{\,\,-}$ , SO $_{4}^{\,\,2-}$ , Ac^???, Ca^2?+?, Na^?+?, K^?+?, Mg^2?+?, and NH $_{4}^{\,\,+}$ in particles were analyzed by ion chromatography. Microtitration was adapted to determine the acidic?Cbasic property and the change of the buffering systems in different pH of the aqueous solution in which the PM is suspended. The major alkalinity and buffer capacity of particles were analyzed and calculated. The average carbonate buffer capacity was 0.3 mmol/g in PM_2.5 and 0.7 mmol/g in PM₁₀. The average acetic acid buffer capacity was 0.1 mmol/g in PM_2.5 and 0.3 mmol/g in PM₁₀. Carbonate and acetic acid are the main species for the buffer capacity in the particle phase. The average mass of carbonate was 71.0 mg/g in PM₁₀ and 46.7 mg/g in PM_2.5. The average mass of acetic acid was 11.2 mg/g in PM_2.5 and 20.0 mg/g in PM₁₀.     

Partitioning between soluble and insoluble fractions of major and trace elements in size-classified airborne particulate matter collected in Tokyo

Airborne particulate matter (APM) is a major air pollutant, and the effect on human health of fine APM (PM2.5) deposited deep inside the lungs has recently become a serious concern. Moreover, soluble constituents may leach from APM, and intensify some health disorders. To identify the soluble chemical constituents of APM, size-classified APM was sampled in central Tokyo, and the elemental compositions of the water-soluble, acid-soluble and insoluble fractions were investigated. The extraction procedure was validated by calculating the mass balance of soluble and insoluble fractions of a standard APM reference material (NIST SRM 1648). Among the major elements, Fe and Ti in APM of all size classes and K in coarse APM were distributed primarily in the insoluble fraction and were inferred to be present as oxides or silicates, whereas Na and Mg in all size classes and K in fine APM were primarily in the water-soluble fraction and were inferred to be have originated mainly from sea salt. Among the trace elements, Zn and Cd in the fine APM (d < 2 microm) had large enrichment factors, indicating an anthropogenic origin, and were distributed primarily in the water-soluble fraction. When fine anthropogenic APM enters into the lungs, leached toxic elements, such as Cd, may adversely affect health. The higher the bonding energy of the monoxide molecule of the element was, the higher its distribution ratio was in the water-soluble fraction. Therefore, many metallic elements in APM were inferred to be present as oxygen-bonded compounds.     

Thermodynamic influences on size fractionated measurements (PM 2.5, PM 10) of ambient aerosols

Mass concentrations of PM 10 and PM 2.5 are planned as new standards for the monitoring of ambient air quality in the European Union. Standard procedure is the removal of particles > 10 microns and > 2.5 microns aerodynamic diameter, respectively, by impaction in a preseparator. Different samplers work according to different principles of flow control. The influence of ambient temperature, pressure and relative humidity on different devices is calculated to estimate the comparability of various aerosol samplers. Therefore, the effects of these ambient factors on the volume flow as well as on the cut-off dp50 are investigated. In a second step, the influence of relative humidity on the flow control device is calculated. The results show that the cut-off shifts (up to 6.4%) for varying ambient conditions. Therefore, the influence on the impaction process should not be neglected and an 'ideal sampler' would measure temperature, pressure and relative humidity and adapt the volume flow to avoid a systematic error in the cut-off.     

Characterisation of particulate matter emissions from the Zimbabwe Mining and Smelting Company (ZIMASCO) Kwekwe Division (Zimbabwe): a ferrochrome smelter

Particulate matter emissions from stack number 2 of a majorferrochrome smelter, Zimbabwe Mining and Smelting Company(ZIMASCO) were characterized and the rates at which the elementsCr, Fe, Cu and Zn and total ferrochrome dust are emitted into theatmosphere were determined. The extent of soil contamination bythe dust deposited around the smelter in the generally prevailingsoutheasterly wind direction around the smelter was carried out.The highest concentrations of Cr and Fe occurred in the fineparticulates of sizes less than 59 m whilst that of Cu and Znoccurred in the coarse particulates of size range 70-100 m.The emission rates from stack 2 were; total ferrochromeparticulates 62.17 kg h^-1, Cr 6.217 kg h^-1, Fe 2.423 kg h^-1, Zn42 mg h^-1 and 6 mg h^-1 for Cu. Particulate matter was emitted at arate of 289 mg m^-3 from stack number 2. This value exceeds thelegal limit of 200 mg m^-3. Chromium and iron are the metalsin the largest amounts. The particles that constitute the largestproportion of the dust were in the range of 58-107.5 m. Thisis a characteristic feature of the particulate matter emissionsfrom ZIMASCO. Soils in the downwind direction from the smelterwere polluted with Cr up to a distance of about 700 m outward fromthe perimeter of the boundary of the smelter.     

Concentrations, enrichment and predominant sources of Sb and other trace elements in size classified airborne particulate matter collected in Tokyo from 1995 to 2004

APM was collected and trace elements existing in the particles were monitored since May 1995 in this study. APM sample was collected separately by size (d < 2 microm, 2-11 microm and >11 microm) on the roof of the university building (45 m above ground) in the campus of Faculty of Science and Engineering, Chuo University, Tokyo, Japan, using an Anderson low volume air sampler. The collected sample was digested by HNO3, H2O2 and HF using a microwave oven, and major elements (Na, Mg, Al, K, Ca and Fe) were measured by ICP-AES, and trace elements (Li, Be, Ti, V, Cr, Mn, Co, Ni, Cu, Zn, As, Se, Mo, Cd, Sb, Ba and Pb) were measured by ICP-MS. It was observed that the APM concentration was higher between the winter and the spring, compared to during the summer. The enrichment factor was calculated for each element in each set of APM (d < 2 microm, 2-11 microm and >11 microm). Seasonal trends of enrichment factors were examined, and the elements were classified into 3 groups according to the common seasonal behavior. It is likely that the elements in the same group have common origins. Toxic pollutant elements (Sb, Se, Cd, Pb and As) were found in small particles with d of <2 microm in concentrated levels. Antimony (Sb) had the highest enrichment factor, and the results suggested that Sb level in APM was extremely high. The origins of Sb were sought, and wastes from plastic incineration and brake pad wears of automobiles were suspected. Each set of APM (d < 2 microm, 2-11 microm and >11 microm) was classified by the shape, and the shape-dependent constituents of a single APM particle were quantitatively measured by SEM-EDX. High concentration of Sb was found in APM <2 microm and square particles. Particles less than 2 microm and square shaped particles were major particles produced by actual car braking experiments. From these experimental results it was concluded that the source of Sb in squared APM <2 microm is considered to be from brake pad wear.     

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.     

Distribution of heavy metals in water, particulate matter and sediments of Gediz River (Eastern Aegean)

The present paper is the first document of heavy metal levels in surficial sediment, water and particulate matter of the Gediz River collected from five different sites in August, October 1998, February, June 1999. The present work attempts to establish the status of distribution and environmental implications of metals in the sediment, water and particulate matter and their possible sources of derivation. The concentrations of mercury ranged 0.037–0.81, 120–430; lead 0.59–1.5, 190–8,100; copper 0.24–1.6, 30–180; zinc 0.19–2.9, 10–80; manganese 30–170, 20–490; nickel 0.39–9.0, 100–510; iron 1.3–687, 100–6,200 μg/l in water and particulate matter, respectively. The maximum values in water were generally obtained in summer periods due to industrial and agricultural activities at Muradiye. The particulate metal concentrations also generally showed increased levels from the upper Gediz to the mouth of the river. Calculation of metal partition coefficients shows that the relative importance of the particulate and the water phases varies in response to water hydrochemistry and suspended solid content, but that most elements achieve a conditional equilibrium in the Gediz River. The metals ranged between Hg: 0.25–0.49, Cr: 59–814, Pb: 38–198, Cu: 15–148, Zn: 34–196, Mn: 235–1,371, Ni: 35–175, and Fe: 10,629–72,387 mg/kg in sediment. The significant increase of metals found in Muradiye suggested a pollution effect, related to anthropogenic wastes. Also, relatively high concentrations of Ni and Mn occurred in sampling site upstream, due to geochemical composition of the sediments. Maximum values of contamination factor for metals were noticed for sediment of Muradiye. The sampling stations have very high degree of contamination indicating serious anthropogenic pollution.     

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.     

Heavy metals concentrations in zooplankton and suspended particulate matter in a southwestern Atlantic temperate estuary (Argentina)

The present work includes part of the first studies of metals concentrations in the zooplankton from a heavily industrialized estuary of Argentina, the Bahía Blanca estuary. Cd, Cu, and Pb concentrations in the zooplankton (macro- and mesozooplankton) and the suspended particulate matter were measured at stations with different degree of pollution. Physicochemical variables and zooplankton composition and abundance were also analyzed. Thus, the aim of the present work was to analyze the spatial and temporal distribution of heavy metals in these two different fractions, and the possible relation among them due to their importance in the biogeochemical cycles of marine environments. Samplings were carried out during a year, from March 2005 to April 2006, every 2 months, at stations located near chemical and petrochemical industries, stations far from these points and one station in an intermediate location. In the mesozooplankton, the mean concentrations of Cd, Cu, and Pb were 3.63?±?1.46, 34.46?±?5.40, and 11.54?±?3.04 μg?g^?1 dry weight (d.w.) respectively, while in the macrozooplankton, 3.20?±?2.28, 21.86?±?4.79, and 8.36?±?1.85 μg?g^?1 d.w. On the other hand, particulate Cd, Cu, and Pb presented a mean concentration of 3.33?±?1.22, 12.75?±?2.67, and 12.53?±?3.20 μg?g^?1 d.w., respectively. Metals’ levels in both the SPM and zooplankton fluctuated throughout the study time and were relatively high in the particulate phase especially for Cu and Pb. Moreover, zooplankton accumulated important concentrations of the three metals. The sources of them are probably the discharges of the industries and domestic sewages located near the estuary.     

Distribution of PM2.5 and PM10-2.5 in PM10 Fraction in Ambient Air Due to Vehicular Pollution in Kolkata Megacity

This research paper aims at establishing baseline PM₁₀ and PM_2.5 concentration levels, which could be effectively used to develop and upgrade the standards in air pollution in developing countries. The relative contribution of fine fractions (PM_2.5) and coarser fractions (PM_10-2.5) to PM₁₀ fractions were investigates in a megacity which is overcrowded and congested due to lack of road network and deteriorated air quality because of vehicular pollution. The present study was carried out during the winter of 2002. The average 24h PM₁₀ concentration was 304 μg/m³, which is 3 times more than the Indian National Ambient Air Quality Standards (NAAQS) and higher PM₁₀ concentration was due to fine fraction (PM_2.5) released by vehicular exhaust. The 24h average PM_2.5 concentration was found 179 μg/m³, which is exceeded USEPA and EU standards of 65 and 50 μg/m³ respectively for the winter. India does not have any PM_2.5 standards. The 24 h average PM_10-2.5 concentrations were found 126 μg/m³. The PM_2.5 constituted more than 59% of PM₁₀ and whereas PM₁₀-PM_2.5 fractions constituted 41% of PM₁₀. The correlation between PM₁₀ and PM_2.5 was found higher as PM_2.5 comprised major proportion of PM₁₀ fractions contributed by vehicular emissions.     

Lead (Pb) and arsenic (As) bioaccessibility in various soils from south China

Serious problems are faced in several parts of the world due to the presence of high concentration of fluoride in drinking water which causes dental and skeletal fluorosis to humans. Nalgonda district in Andhra Pradesh, India is one such region where high concentration of fluoride is present in groundwater. Since there are no major studies in the recent past, the present study was carried out to understand the present status of groundwater quality in Nalgonda and also to assess the possible causes for high concentration of fluoride in groundwater. Samples from 45 wells were collected once every 2 months and analyzed for fluoride concentration using an ion chromatograph. The fluoride concentration in groundwater of this region ranged from 0.1 to 8.8 mg/l with a mean of 1.3 mg/l. About 52% of the samples collected were suitable for human consumption. However, 18% of the samples were having less than the required limit of 0.6 mg/l, and 30% of the samples possessed high concentration of fluoride, i.e., above 1.5 mg/l. Weathering of rocks and evaporation of groundwater are responsible for high fluoride concentration in groundwater of this area apart from anthropogenic activities including irrigation which accelerates weathering of rocks.     

Source analysis of particulate matter associated polycyclic aromatic hydrocarbons (PAHs) in an industrial city in northeastern China

Particle-associated polycyclic aromatic hydrocarbon (PAH) concentrations were investigated at eight sampling sites during cold periods where heating is used (heating period) (February to March, 2005) and warm periods where heating is not required (non-heating periods) (August to September 2006) in the urban area of Anshan, an iron and steel city in northeastern China. Eleven PAH species were measured using GC-MS. The total average concentrations of PAHs ranged from 46.14 to 385.60 ng m(-3) in the heating period and from 5.28 to 146.40 ng m(-3) in the non-heating period. The lowest concentration of ∑PAHs was observed at Qianshan, a monitoring site far from the city and industrial area, and the highest concentration occurred in the site located at the factory area of Anshan Iron and Steel Incorporation. Moreover, ambient PAH profiles were studied and high molecular weight PAH (including 4-6 rings) species occurred in the high fractions. Toxic equivalent factors analysis gave the potential carcinogenic risks in Anshan. For the heating sampling period, BaP equivalent concentration is in the range of 41.98 to 220.83 ng m(-3), and 9.23 to 126.00 ng m(-3) for the non-heating sampling period. By diagnostic ratio analysis, traffic emission and combustion (coal or biomass) were potential sources for PAHs in Anshan. Finally, PCA results indicated the major sources were vehicle emission, steel industry emission, and coal combustion for both heating and non-heating seasons, which agreed with the results from the diagnostic ratio analysis.     

RELEVANT ASPECTS OF AIR QUALITY IN OPORTO (PORTUGAL): PM10 AND O3

The air quality Framework Directive (FWD) and the correspondent Daughter Directives defined the new strategy for air quality management in Europe. In general, the new standards are more restrictive than those established by the previous legislation. In Portugal, some difficulties can be previewed to achieve those new standards. Thus, this paper aims at evaluating the impact of application of the FWD to Oporto Metropolitan Area in what concerns to the most critical air pollutants in the area (PM₁₀ and O₃). The specific objectives were: i) to analyse the concentration exceedances between 1999 and 2001; ii) to identify the main emission sources; iii) to evaluate the possibility of a new redistribution of the existing monitoring sites; iv) to contribute to the definition of a new strategy for air quality management. The results showed that; i) the standard values for PM₁₀ and O₃ were largely surpassed, possibly concluding that the FWD application implies a strong impact on the air quality management strategies; ii) the main emission sources (road traffic and the neighbour stationary sources localised upwind) affect all the Metropolitan area through intra-region pollutant transport; iii) it is safer maintaining the site localisation to avoid previewing exceedances through mathematical correlations; iv) the reduction of PM₁₀ and of ozone precursors must be performed considering new technologies for cleaner production and gaseous depuration, a rigorous urban and territory planning, the creation of an efficient public transport network and the definition of strict measures for car maintenance.