Air pollution at the Bily Kriz mountains in the Czech Republic

An evaluation of air pollution at the Bily Kriz mountains in the Czech Republic is given. Annual daily concentrations of sulphur dioxide (SO₂), nitrogen oxides (NO_x), particulate matter of size 10 mm (PM₁₀) and ozone (O₃) measured in the years 1994–2000 are presented. Air pollution at Bily Kriz is assessed with the reference to the European Union Directives and the standards adopted by the Czech Republic. In general, the concentrations of air pollutants were lower in 1996 for ozone and decreased for SO₂, NO_x and PM₁₀ from 1994. The daily values of SO₂ and PM₁₀ exceeded the European Union limits in approximately 0.0% and 5.5% of cases, respectively. The values of ozone exceeded the limits for the considered period.     

Atmospheric particulate matter in the city of Sao Carlos/SP, Brazil

This paper presents experimental data and source apportionment simulations on particulate matter (PM₁₀ and PM_2.5) in the atmosphere of Sao Carlos/SP, Brazil. Both a Hi-vol sampler equipped with glass fibre filters and a Dichotomous sampler with nucleopore filters were used. The collected material was analysed for total carbon, using a thermometric method, and for traces of several chemical species, using X-ray fluorescence spectroscopy. Source apportionment estimations were made with a chemical mass balance receptor model software (CMB8), with source profiles taken and adapted from the literature. The results indicate that both PM₁₀ concentration and source apportionment vary seasonally, and that vegetative burning can be a significant source of PM₁₀ in the dry season     

Separate determination of PM10 emission factors of road traffic for tailpipe emissions and emissions from abrasion and resuspension processes

Little is known about the relevance of mechanically produced particles of road traffic from abrasion and resuspension processes in relation to the exhaust pipe particles. In this paper, emission factors of PM₁₀ and PM₁ for light and heavy-duty vehicles were derived for different representative traffic regimes from concentration differences of particles and nitrogen oxides (NO_x) in ambient air upwind and downwind of busy roads, or alternatively of kerbsides and nearby background sites. Hereby, PM₁ was interpreted as direct exhaust emissions and PM₁₀-PM₁ as mechanically produced emissions from abrasion and resuspension processes. The results show that abrasion and resuspension processes represent a significant part of the total primary PM₁₀ emissions of road traffic. At sites with relatively undisturbed traffic flow they are in the same range as the exhaust pipe emissions. At sites with disturbed traffic flow due to traffic lights, emissions from abrasion/resuspension are even higher than those from the exhaust pipes.     

Measurement of atmospheric particles and anionic species across central Taiwan

The ambient air concentrations and fluxes of various anionic species were sampled by MOUDI, TSP and dry deposition plates at a traffic sampling site in Taichung, central Taiwan. In the sampling period, from September to December 2000, the ambient air particle concentrations (PM₁, PM_2.5, PM₁₀ and TSP) were lower in the September than in the other three months (October to December). The reason is that the northwest wind brought more particles (diameter less than 10 μm) and the higher wind speed caused higher dry deposition fluxes and TSP concentrations in the last three months. The anion species percentages of TSP were 0.24%, 13.7%, 0.52%, 12.0%, 18.9'% and 54.6% for F^-, Cl^-, Br^-, NO₂^-, NO₃^- and SO₄^2-, respectively. The results revealed that SO₄^2-, NO₃^-, Cl^- and NO₂^- were the dominant species at the traffic sampling site. The ion-size distributions of Cl^-, NO₂^- and NO₃^- were unimodal, the main peak being between 3.2 and 5.6 μm. In contrast, the size distribution of SO₄^2- was bimodal, with the main peaks in the particle size ranges 0.32.0.56 μm and 3.2.5.6 μm. The ambient average particle dry deposition flux was 6.28 μg/m2/s, and the dry deposition fluxes were 0.01, 94.6, 0.05, 34.7, 72.2 and 376.4 ng/m2/s for F^-, Cl^-, Br^-, NO₂^-, NO₃^- and SO₄^2-, respectively. The dry deposition velocities were 3.10, 0.03, 3.67, 0.05, 1.54, 2.03 and 3.67 cm/s for F^-, Cl^-, Br^-, NO₂^-, NO₃^- and SO₄^2-, respectively.     

Trends in air quality and population exposure in Santiago, Chile, 1989–2001

This study focused on establishing trends in the period 1988–2001 in PM_2.5, PM₁₀ and ozone concentrations in Santiago, Chile, and linking those to population exposure. There is strong seasonality in the concentration levels, driven by prevailing meteorological conditions, with the concentration of particulates peaking at the beginning of winter, whereas the ozone concentration is highest during the summer. The levels of PM_2.5 and PM₁₀ have substantially decreased since the late 1980s and so has the population exposure. Nevertheless, the majority of the population is still exposed to annual average levels that are above standard values. The situation with ozone exposure is different; no substantial decrease can be observed in the data. If anything, certain parts of Santiago, notably the south-east, have shown increased levels of ozone. Overall population exposure indicates that the average person was more at risk of ozone in the year 2000 than they were in 1993.     

Characteristic study of particulates and metallic elements at an urban sampling site in Taichung, central Taiwan

Atmospheric total suspended particulate concentrations and metallic element concentrations were measured at three locations, characteristic of urban, suburban and rural sites. The sampling period was from July 2000 to August 2000. The results indicated that the urban sampling site had the highest total suspended particulate concentrations (average 108.61μ1m3), followed by the suburban site (average 60.11μ1m3) and the rural site (average 53.31μ1m3). The average PM_2.5 concentrations (24.11μ1m3) were higher than the PM_2.5-10 concentrations (12.81μ1m3) at the urban site. The average distributed ratios for PM_2.5/PM_2.5-10 were about 1.29, 1.53, 0.12, 1.12 and 2.31 for Pb, Zn, Fe, Ni and Cr, respectively. The average total suspended particulate mass ratios for daytime and nighttime were about 1.72. As for the elements Cu, Pb, Zn, Fe, Ni and Cr, these ratios were about 0.63, 0.97, 0.54, 1.66, 0.53 and 1.12, respectively. The total suspended particulate daytime concentrations of Pb and Zn were positively correlated (R = 0.925) at the urban sampling site. The elements Ni and Cr were positively correlated both during the daytime (R = 0.648) and the nighttime (R = 0.511), revealing that they came from the same emission source during daytime and nighttime, at the urban sampling site.     

Annual simulation of secondary pollution over northern Italy

A secondary pollution modelling system for simulating airborne dispersion and chemical reactions is applied over a regional scale domain located in the North-West of Italy, where urban and industrial areas are present. It was found an overestimation of NO₂ in the urban areas, probably due to an underestimation of the vertical diffusivity; the analysis of O_X confirms that the discrepancies in O₃ and NO₂ are mainly due to local scale effects; the model shows a general underestimation of the observed PM10 concentrations due to the uncertainties in the emission inventories, spatial resolution, and the adopted aerosol modelling approach.     

Roadside particulate levels at 30 locations in the Kathmandu Valley, Nepal

Roadside particulate levels (PM₁₀) at 30 locations throughout the Kathmandu Valley, Nepal are reported. There were seven sampling cycles from January to December 1999. PM₁₀ levels ranged between 1000 and 6000 μ/m3 for 1-h sampling. There was no consistent trend in PM10 levels with respect to monitoring cycle, average precipitation or wind speed. There is no WHO guideline for PM₁₀ (no safe exposure threshold), but the EPA 24-h standard is 150 μ/m3. The major sources of roadside PM₁₀ include dust re-suspension from vehicular movement and human activity, and particulate emissions from old vehicles. Other sources of PM₁₀ in the valley include cement and brick factories. Studies are currently being conducted to determine the lead content of PM₁₀ from roadside samples. Additional studies are warranted to assess the potential adverse human health effects of acute or chronic exposure to high particulate levels reported in this study.     

Metallic elements in particulates released during incense-burning at Tzu Yun Yen temple, Taichung, Taiwan

Concentrations of ambient suspended particulates were measured at Tzu Yun Yen temple (120°, 34′ 10”E; 24°, 16′, 12”N), using a Universal sampler and dry deposition plates. The temple is a characteristic incense-burning and semi-open sampling site. PM_2.5 concentrations for Period 1 (average 901μg/m3) were higher than those for Period 2 (average 701μg/m3). Results for average PM_2.5-10concentrations showed equal distributions in Period 1 and Period 2. Average ratios of PM_2.5/ PM₁₀ were higher in Period 1 (74%) than Period 2 (71%). In addition, the suspended particulate (PM₁₀) elements concentrations during Zhong Yuan Jie, and the first and 15th days of nong li for each month (Chinese lunar calendar) were all higher than during non-Zhong Yuan Jie and non-first and non-15th days. Furthermore, the dry deposition velocities of manganese in fine particulates (PM_2.5) and suspended particulates (PM₁₀) were 1.43 and 0.751cm/s, respectively, and the dry deposition velocities of cadmium in fine particulates (PM_2.5) and suspended particulates (PM₁₀) were 1.86 and 0.991cm/s, respectively.     

The study of temple and pastureland particle-bound polycyclic aromatic hydrocarbons concentrations in central Taiwan

The concentrations of polycyclic aromatic hydrocarbons in the atmosphere were measured simultaneously at Tzu Yun Yen temple and Tung Hai University pastureland in Taichung, central Taiwan. At both sites, 24 h samplings were performed between August 2001 and December 2001. The results indicated that high molecular mass polycyclic aromatic hydrocarbons are predominant at the Tzu Yun Yen temple sampling site. Moreover, the PM_2.5 (fine particulate) fraction of total polycyclic aromatic hydrocarbons was higher than that of the PM_2.5-10 (coarse particulate) fraction by a factor of about 1.48 at the temple sampling site. This ratio was 1.24 for the pastureland environment.     

Air pollution and the influence of sources on Paulinia (Brazil) and surroundings

The air quality in the industrial area and surroundings of the city of Paulinia (state of Sao Paulo, Brazil) has been investigated by analysing the concentration of air pollutants (SO₂, PM₁₀, NO, NO₂, CO and ozone) and identifying the main sources of air pollution. A mobile pollutant monitoring unit was used to collect the data at five different sites from November 2000 to July 2002. Critical pollutants were determined based on air quality standards, and sources were identified by principal component analysis. Photochemical reactions play an important role in Paulinia's air pollution: three out of five monitored sites showed levels exceeding the standard air quality of ozone. SO₂ and PM₁₀ appeared as pollutants deserving special attention. All the monitored sites showed vehicles and industrial plants (which release SO₂) to be significant sources of pollution. Depending on the location, ozone was related mainly with vehicular or industrial sources.     

Observation based analysis for the determination of equilibrium time constant between ammonia, acid gases, and fine particles

Experimental measurements of ammonia, acid gases, and the inorganic components of atmospheric aerosols were made at a commercial hog farm in eastern North Carolina from May 1998 to June 1999 by an annular denuder system (ADS). The ADS consisted of a cyclone separator, one diffusion denuder coated with sodium carbonate, another diffusion denuder with citric acid, and a filter pack containing Teflon and nylon filters in series. The equilibrium time constant for transfer between ammonia, acid gases, and aerosol phase of ammonium nitrate and ammonium chloride was determined based on kinetic rate constants (k_N as the rate constant of ammonium nitrate aerosol: 2.04 × 10^-4 m³/µmole/sec; k_Cl as the rate constant of ammonium chloride aerosol: 3.44 × 10^-4 m³/µmole/sec) and the observed inorganic components of atmospheric aerosols. The equilibrium time constant was determined based on kinetic rate constants and the observed inorganic components of atmospheric aerosols. The equilibrium time constant has a wide range of values, with an average value of 15.26 (±10.94) minutes for ambient equilibrium time between ammonia, nitric acid gas and ammonium nitrate aerosol; and 8.22 (±6.81) minutes for ammonia, hydrochloric acid, and ammonium chloride. Significant correlations were determined between comparisons of equilibrium time constant estimates with meteorological parameters, such as ambient temperature and relative humidity. The predicted chemical compositions in the particle by EQUISOLV II Model are in good agreement with the observed chemical composition at the experimental site.     

Sampling errors in the study of acid gases and anion species in atmospheric aerosols

Atmospheric acid aerosols were sampled by two annular denuder systems (ADS) and a micro-orifice uniform deposit impactor (MOUDI) at a traffic site in central Taiwan. Theoretical analysis showed that the relative artifact for HNO₃ gas sampling was about 0.53 when the initial HNO₃ concentration was under 0.2 µg/m³ and should be considered carefully. The concentrations of gaseous acid at the traffic sampling site were higher than those in the other study. The size distributions of acid aerosols were unimodal for Cl^-, NO₂^-, and NO₃^-, and bimodal for SO₄^2-. The dominant acid ions in particles less than 18 µm were SO₄^2-, NO₃^-, NO₂^- and Cl^-.     

Monitoring of phytoplankton biomass and nutrients in a polluted stream

The spatial and temporal variations in the concentrations of nutrients (NH₄⁺, NO₂⁻, PO₄³⁻, SiO₄⁻) and chlorophyll a were monitored simultaneously in a slow-flowing watercourse (Saricay Stream, Turkey), which runs in a rural–urban gradient. Chlorophyll a concentrations ranged between 0.044 μg l^-1 and 206.15 μg l^-1 and, in general, the higher concentrations of chlorophyll a and ammonium were measured downstream of the raw sewage outfalls. Nitrate was by far the most abundant form of inorganic nitrogen, and its concentration ranged between 411.71 μM and 87.25 μM. Silicates and phosphates were always potentially limiting to biomass relative to nitrogen. Agricultural run-off and point discharges from urban sources greatly affected the chemical composition of the water in the Saricay Stream and drove the system towards eutrophication.     

Assessment of particulates in the urban atmosphere of Sao Carlos, Brazil

A survey on the concentration of particulate matter in the urban atmosphere was carried out in the city of Sao Carlos, Brazil. Five sites were selected for data collection one in the city centre (high concentration of people and automotive vehicles), three in industrial areas, and one at the interface with the countryside. The particle size distribution and mass concentration, temperature, humidity and wind velocity were measured at each site. In the city centre, the concentration of the particles smaller than 10 μm (PM₁₀) was also measured. The particle size distribution was obtained with a laser scattering particle counter. The total and PM₁₀ concentrations were obtained with high volume samplers. The tests were performed for 75 consecutive weeks. The results show that the particle concentration is sensitive to seasonal conditions. During autumn and winter, which is the drier and windy period of the year, larger particles were dispersed, leading to higher concentrations, both total and PM₁₀. The relative humidity varied with the schedule of sampling and with the season the autumn and winter weeks were much drier than the other periods. Higher rainfall levels coincided with lower particle concentrations. All these results are statistically significant.     

Studies of air quality predictors based on neural networks

In recent years, urban air pollution has emerged as an acute problem because of its negative effect on health and living conditions. Regional air quality problems, in general, are linked to violations of specified air quality standards. The current study aims to find neural network based air quality predictors, which can work with a limited number of datasets and are robust enough to handle data with noise and errors. A number of available variations of neural network models, such as the Recurrent Network Model (RNM), the Change Point Detection Model with RNM (CPDM), the Sequential Network Construction Model (SNCM), the Self Organising Feature Model (SOFM), and the Moving Window Model (MWM), were implemented using MATLAB software for predicting air quality. Developed models were run to simulate and forecast based on the annual average data for 15 years from 1985 to 1999 for seven parameters, viz. VOC, NO_x, CO, SO₂, PM₁₀, PM_2.5 and NH₃ for one county of California, USA. The models were fitted with first nine years of data to predict data for remaining six years. The models, in general, could predict air quality patterns with modest accuracy. However, the SOFM model performed extremely well in comparison with the other models for predicting long-term (annual) data.     

Exploratory study of some potential environmental impacts of CO2 sequestration in unmineable coal seams

An initial investigation into the potential environmental impacts of CO₂ sequestration in unmineable coal seams has been conducted, focusing on changes in the produced water during enhanced coalbed methane (ECBM) production, using a CO₂ injection process (CO₂-ECBM). A high volatile bituminous coal, Pittsburgh No. 8, was reacted with synthetic produced water and gaseous carbon dioxide at 40°C and 50 bar to evaluate the potential for mobilisation of toxic metals during CO₂-ECBM/sequestration. Microscopic and X-ray diffraction analysis of the post-reaction coal samples clearly show evidence of chemical reaction and chemical analysis of the synthetic produced water shows substantial changes in composition. These results suggest that changes to the produced water chemistry and the potential for mobilising toxic trace elements from coal beds are important factors to be considered when evaluating deep, unmineable coal seams for CO₂ sequestration.     

Spatial and diurnal variations in concentration of atmospheric NOx along urban-rural roadways in Nanjing, Southeastern China

Atmospheric NO_x concentrations (including NO₂ and NO) on the roadside environments of urban trunk, belt highway and suburban road as well as a reference in a forest area were measured. NO_x concentrations on roadside environments tended to be higher than that on the reference. With the exception of suburban road, NO_x concentrations over both of the urban trunk and belt highway exceeded the limited value of National Air Environmental Quality Standards. Gradient measurement of NO_x on the downwind side of the belt highway shows that it declined to background level over 100 m from the road edge.     

Treatment of reactive dyes and textile finishing wastewater using Fenton's oxidation for reuse

Fenton's oxidation (FO) was used to decolourise and degrade some reactive dyes (Remazol Black 5, Remazol Red, Remazol Blue, Remazol Yellow) and raw textile finishing industry effluents (S1, S2, S3) containing mainly reactive dyes. The operational conditions for pH varied between 2.5 and 4.0 while temperature ranged from 30°C to 50°C. The concentrations of FeSO₄ and H₂O₂ varied to a wide range (200–600 mg/l of FeSO₄, 300–1000 mg/l of H₂O₂) depending on the type of the dyes and their mixture and textile additives used in the process. FO is highly effective for colour removal (>99%) for reactive dyes and (87–94%) for textile finishing wastewater. It can be applied as a pretreatment and the remaining total dissolved solids (TDS) can be removed by an additional advanced process, e.g. membrane process.     

Analysis and interpretation of the monitoring data for C2–C11 hydrocarbons in the atmosphere of a rural Portuguese site

This paper focuses the application of a measurement technique for determining atmospheric C₂–C₆ hydrocarbons after canister sampling and analysis by gas chromatography/flame ionisation detection (GC/FID), as well of an adsorption-sampling technique for C₆–C₁₁ compounds and GC/FID analysis after thermal desorption and cryogenic concentration. Tens of samples collected at Giesta, a rural area located 20 km to the SE of the coastal Portuguese city of Aveiro, were analysed. The characterisation of C₂ C₁₁ hydrocarbons is presented, considering seasonal variations, diurnal cycles, the influence of air masses and different photochemical conditions. Ratios between hydrocarbons and principal components analysis were applied to differentiate between biogenic and anthropogenic sources.