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^-.     

Modelling changes of aerosol compositions over Belgium and Europe

Seasonal changes in aerosol compositions over Belgium and Europe are simulated with an extended version of the EUROS model. EUROS is capable of modelling mass and chemical composition of aerosols in two size fractions (PM_2.5 and PM_10-2.5). The chemical composition is expressed in terms of seven components: ammonium, nitrate, sulphate, primary inorganic compounds, elementary carbon, primary organic compounds and Secondary Organic Compounds (SOA). A comparison of modelled and measured aerosol concentrations showed that modelled concentrations are generally consistent with observed concentrations. The chemical composition of the aerosol showed a strong dependence on the season. High aerosol concentrations during the summer were mainly due to high concentrations of the secondary components nitrate, ammonium, sulphate and SOA in the size fraction PM_2.5. In contrast, during autumn and winter, increased PM-concentrations were mainly due to higher concentrations of primary components, especially in the size fraction PM_10-2.5.     

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.     

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.     

Nitrification of centrate from dewatering of anaerobically digested sludge

Nitrification of anaerobically digested sludge centrate was studied in bench-scale suspended growth and fixed film enhanced suspended growth systems at temperatures of 10.5-28.5°C and pH values of 6.0-9.1. Nitrification followed zero-order kinetics in both systems, and ammonia removals in excess of 99% were observed. The temperature dependency of the suspended growth nitrification rate observed under not fully acclimated biomass conditions at pH between 6.8 and 8.5, was expressed as k_T = k₂₀θ^T-20where k₂₀ and θ were found to be 0.34 mg NH₃-N/MLVSS-d and 1.033, respectively. The nitrification rate in the fixed film enhanced suspended growth system involving styrofoam pads ranged from 0.11 to 0.13 mg NH₃-N/mg MLVSS-d at temperatures of 21.5-25°C and pH values of 7.8-8.6. The process contained suspended solids in the range of 10-20 mg/l.     

Differential water quality in confined and free-flowing water bodies, Lebanon

Integrated management of water resources is a major critical issue to be addressed in combating water stress in developing countries, such as Lebanon. At present, surface water is not properly used in Lebanon. This emphasises the importance of assessing surface water quality as a projected means to increase water availability. This study involves two different water bodies, the freely flowing Nahr-Ibrahin River and the Qaraaoun Reservoir, an impoundment of the Litani River. Water samples were collected from 16 chosen sites of each water body at four different dates during the dry season. Measured water parameters were temperature, pH, conductivity, BOD, HCO₃^-, Ca²⁺, Mg²⁺, Cl^-, SO₄^2-, PO₄^3-, NO_{3-, NH3, Fe, Mn, Zn, Pb, and Cd. Statistical analysis of the data revealed significant differences in water quality. The differences could be attributed to the fact that whereas the Qaraaoun reservoir is receiving domestic waste discharges that lead to an increase in the CO2 content and a pH decrease, the Nahr-Ibrahim River is influenced by agricultural runoffs and industrial discharges that increase the pH values. Consequently, the water metal speciation of the two water bodies was different. The study indicated that the differential quality of the two water bodies could be attributed to the nature of the water resources and exposure to contaminants. This is crucial in recommending intervention studies to protect quality and promote the role of surface water use, as an integrated component of water management in Lebanon.}     

Time-resolved ammonia measurement in vehicle exhaust

The objective of this study was to identify the influence of sampling and analytical approach on the quality of NH3 emission data of a gasoline-fuelled three-way catalyst vehicle. NH₃ concentration measurements have been performed in the tailpipe and in the diluted exhaust after a constant volume sampling (CVS) system during five different test cycles. Chemical ionisation mass spectrometry (CI-MS) and Fourier transform infrared spectroscopy (FTIR) were used to acquire ammonia concentrations in real-time. Independently, NH₃ emission rates were determined by continuous absorption of a flow-proportional sample of exhaust gas in diluted sulphuric acid and subsequent ion chromatography (IC). Ammonia emission rates ranged from 22–94 mg km^-1. The results of the three compared techniques are in good agreement. Furthermore, time-resolved ammonia emission profiles recorded by CI-MS and FTIR coincided with respect to emission levels as well as emission dynamics. However, in the dilution tunnel, severe ammonia adsorption was observed leading to long lasting memory effects or even analyte loss. Therefore, neither ammonia real-time emission data nor NH₃ emission rates should be acquired after a CVS system.     

Temporal variability of the precipitation chemistry in the forest area of Istanbul, Turkey

The chemical compositions of precipitation show temporal and spatial variability. It is important to determine the temporal variation of the chemical composition of rainwater for estimating the impacts of pollutants on the forest. In this study, the 34 rainwater samples are collected using, for the first time, the specially designed collectors between November 1997 and March 1998 in Istanbul University, Faculty of Forestry at Bahcekoy, Istanbul in Belgrad Forest. The sequentially collected samples are analysed for major ions concentrations and pH estimations. The pH values for all samples vary from 5.1-7.6. In general, the concentration of all rainwater samples decrease with time. Furthermore, it is estimated that the average Ca²⁺) (1943.0 µeql^-1) and SO₄^2- (887.3 µeql^-1) concentrations are extremely high during the first ten minutes of the precipitation event.     

Effects of organic loading and oil-grease for the treatment of edible oil effluent in a pilot-scale upflow anaerobic sludge blanket process

In this study, Karadeniz Birlik Dogan Erdil vegetable oil factory, Elazig City, Turkey, was selected as representative of this sector. During the first part of the test programme, the quality of raw effluents was investigated. The removals of COD and oil-grease were above 85% at organic loadings between 1.62 and 7.83 kg COD m^-3 d^-1 at hydraulic retention times of 2.0 and 2.5 days. The conversion rates of the removed COD into methane gas were between 0.24 and 0.361 g CH₄ (g COD)^-1.     

Preliminary studies of the oxidation of arsenic(III) by potassium ferrate

The Pollutant Standards Index (PSI) was developed in the USA to give the public an overall assessment of the air quality on a regular basis. Currently, the PSI does not include the synergistic effects of the major air pollutants. Synergism applies when the damage caused by two or more pollutants, either to human health or property, is greater than the effect or damage caused by each individual pollutant acting alone. The purpose of this work is to develop a methodology that would take into account the synergistic effects of the priority air pollutants, and therefore give us a better understanding of the severity of the damage caused by these pollutants. The equation suggested is D(P1,P2,P3,P4,P5) = C1^A C2^B C3^C C4^D C5^E. If it is assumed that the weight constants A to E are equal to one (all pollutants contribute equally to the damage), the equation becomes D (P1,P2,P3,P4,P5) = K·C1·C2·C3·C4·C5 where the constant K represents a conversion factor between the PSI scale and the new Synergistic Theory scale. The value of K is to be determined experimentally by finding the threshold value in the synergistic scale and dividing the threshold value of the PSI scale (100) by this number K = 100/SSC1_threshold where SS_threshold is the Synergistic Scale threshold value.     

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.     

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.     

Source contribution of atmospheric aerosols in Bangkok metropolitan area by CMB8 receptor model

The CMB₈ model was applied for source apportionment of particulate matter in Bangkok area. The 24 h of ambient data were collected and analysed for elemental composition during December 1996 to January 1997 by high volume air samplers at a station in Bangkok, Thailand. Seven source profiles and the average mass concentrations of 42 ambient data were used to run the chemical mass balance (CMB₈) model. The source apportionment by CMB₈ gave similar results comparing with factor analysis – multiple regression (FA–MR) model of the same data. The results revealed that major sources of particulate matter in Bangkok were: soil (33%), road dust (33%) and automobile (15%). The minor source contributions were: sea salt (4.34%), refuse incineration and biomass burning (0.84%), steel mill (0.62%) and fuel oil combustion (0.35%). The lack of source profile for biomass or open burning in Bangkok resulted in much lower predicted contribution of this source when compared to that from FA–MR. When apply this CMB₈ model with daily ambient data, the result revealed that one fourth of daily CMB₈ source apportionment had high value of ² (>4). These exceedance values of Chi² also point out that one of the selected sources (biomass burning) may not be the true contributing sources. Presumably, accurate biomass burning source profile is needed to improve the CMB calculation of source contributions for particulate matter in Bangkok metropolitan area.     

Measurement of ammonia emissions using various techniques in a comparative tunnel study

A field-based intercomparison study for ammonia measurements was conducted using seven analytical methods. It included sulphuric acid impinger, citric acid denuder, differential optical absorption spectroscopy (DOAS), Fourier transform infrared spectroscopy (FTIR), photoacoustic spectroscopy (PAS), and continuous aqueous extraction followed by measurement of conductivity (Airrmonia). Measurements were done at the entrance and the exit of the Gubrist highway tunnel near Zurich, Switzerland. For DOAS, FTIR, PAS and Airrmonia, 24 hour means were calculated based on a time resolution of 10 minutes. At the tunnel exit, all 24 hour averages were within 13%, and the continuous data of the time-resolved methods agreed well. At the tunnel entrance, a slightly reduced method comparison included four methods, and daily mean values agreed within 23%. Ammonia emission factors, based on 4 weeks of continuous measurements with the Airrmonia, were 31 ± 4 mg km^-1 for light-duty vehicles and 14 ± 7 mg km^-1 for heavy-duty vehicles.     

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.     

Chemical coupling between ammonia, acid gases, and fine particles

The concentrations of inorganic aerosol components in the fine particulate matter (PM(fine)< or =2.5 microm) consisted of primarily ammonium, sodium, sulfate, nitrate, and chloride are related to the transfer time scale between gas to particle phase, which is a function of the ambient temperature, relative humidity, and their gas phase constituent concentrations in the atmosphere. This study involved understanding the magnitude of major ammonia sources; and an up-wind and down-wind (receptor) ammonia, acid gases, and fine particulate measurements; with a view to accretion gas-to-particle conversion (GTPS) process in an agricultural/rural environment. The observational based analysis of ammonia, acid gases, and fine particles by annular denuder system (ADS) coupled with a Gaussian dispersion model provided the mean pseudo-first-order k(S-1) between NH(3) and H(2)SO(4) aerosol approximately 5.00 (+/-3.77)x10(-3) s(-1). The rate constant was found to increase as ambient temperature, wind speed, and solar radiation increases, and decreases with increasing relative humidity. The observed [NH(3)][HNO(3)] products exceeded values predicted by theoretical equilibrium constants, due to a local excess of ammonia concentration.     

Measurement of atmospheric fluxes of radionuclides at a UK site using both direct (rain) and indirect (soils) methods

Direct measurements of radionuclide tracers are useful tools for correcting proxy fluxes that are subject to post depositional changes. An analytical methodology was designed for the measurement of ²¹⁰Pb and ⁷Be in rainwater. Atmospheric inputs of the radionuclides to Cumbria (UK) were recorded. Rainwater fluxes were then compared with measurements from soil cores. The annual deposition from April 1997 to March 1998 of ²¹⁰Pb and ⁷Be was 165 ± 8 Bq m^-2 and 3912 ± 120 Bq m^-2, respectively, compared to an indirect ²¹⁰Pb flux of 148 ± 7 Bq m^-2 yr^-1 calculated from soil core records.     

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.     

Preparation, characterisation and testing of photocatalytic polymeric membranes with entrapped or suspended TiO2

Various cellulose triacetate (CTA) or polysulfone (PSf) membranes with entrapped polycrystalline TiO₂ were prepared by using different methods of the so-called phase inversion process. Porosity and permeability of the membranes increased by increasing the amount of entrapped TiO₂ while rejection decreased. The photoactivity of entrapped TiO₂ for the degradation of congo-red was compared with that of the same quantity of suspended TiO₂ and the results indicated that TiO₂ was always more efficient when used in suspension. A hybrid configuration consisting of a continuous membrane photoreactor with the photocatalyst in suspension showed to be the most promising one.     

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.