Roadside BTEX and other gaseous air pollutants in relation to emission sources

Hourly concentrations of benzene, toluene, ethylbenzene, m,p-xylenes, and o-xylene (BTEX) plus CO, NO_x, SO₂ were monitored at roadsides simultaneously with the traffic volume during the dry season of 2004, in Hanoi, Vietnam. The selected three streets included Truong Chinh (TC) with high traffic volume, Dien Bien Phu (DBP) with low traffic volume, and Nguyen Trai (NT) with high traffic volume running through an industrial estate. BTEX were sampled by SKC charcoal tubes and analyzed by GC–FID. Geometric means of hourly benzene, toluene, ethylbenzene, m,p-xylenes and o-xylene are, respectively, 65, 62, 15, 43, and 22 μg m⁻³ in TC street; 30, 38, 9, 26, and 13 μg m⁻³ in DBP street; and 123, 87, 24, 56, and 30 μg m⁻³ in NT street. Levels of other gaseous pollutants including CO, NO_x, and SO₂, measured by automatic instruments, were low and not exceeding the Vietnam national ambient air quality standards. BTEX levels were comparatively analyzed for different downwind distances (3–50 m) from the street, between peak hours and off-peak hours, as well as between weekdays and weekend. Results of principal component analysis suggest that the gaseous pollutants are associated with different vehicle types.     

成都市餐饮源大气污染物排放清单研究

为全面、准确地获得成都市餐饮源大气污染物排放清单,针对成都市社会餐饮、家庭餐饮和食堂餐饮分别选择监测对象进行细颗粒物(PM2.5)、非甲烷总烃(NMHCs)、油烟、氮氧化物(NOx)、SO2和CO 6种大气污染物排放浓度监测.分别按照用油量、就餐人次和灶头风量3种核算依据计算了6种大气污染物的排放因子,并计算成都市餐饮...     

Comparison among air pollutants, meteorological conditions and some chemical parameters in the transplanted lichen Usnea amblyoclada

The response of Usnea amblyoclada (Müll. Arg.) Zahlbr. to real concentrations of atmospheric pollutants measured by two automatic monitoring stations, was studied in Córdoba City, Argentina. The influence of different weather conditions on the biomonitor's response was also assessed. The concentration of chlorophyll a, chlorophyll b, hydroperoxy-conjugated dienes, and malondialdehyde were quantified in lichen thalli collected from a clean area and in transplanted thalli after 1 month of exposure in an urban area, from April to October, 1996. The dry weight/fresh weight, chlorophyll b/chlorophyll a and phaeophytin a/chlorophyll a ratios were also calculated. Data sets were evaluated by two-way analysis of variance and correlation analysis. It was observed that hydroperoxy-conjugated dienes, malondialdehyde, chlorophylls, and pigment degradation increase during winter-time, when higher levels of suspended particles, non-methane hydrocarbons, hydrogen sulfide and ozone were also measured. These findings would be connected mainly with meteorological conditions, as most pollutants did not exceed prescribed threshold levels.     

Chemical response of the lichen Punctelia subrudecta (Nyl.) Krog transplanted close to a power station in an urban-industrial environment

The lichen Punctelia subrudecta (Nyl.) Krog was transplanted to 22 biomonitoring sites in a northwestern area of Córdoba city, Argentina and tested for chlorophyll a, chlorophyll b, phaeophytin a, soluble protein, hydroperoxy conjugated dienes (HPCD), malondialdehyde (MDA) concentration and sulphur accumulation. A pollution index (PI) was calculated for each biomonitoring site. The biomonitoring sites were set according to (1) traffic levels, (2) industrial density and (3) distance of the power station close to each site. The biomonitor's chemical response was associated with industries as well as power stations. Significant differences were observed in sulphur content, MDA concentration and PI values in lichen material transplanted to sites with different industrial densities. The higher values for these parameters were found at sites with high industrial levels. At the same time, significant differences were detected for sulphur content in samples at different distances from the power station, with higher accumulation in samples located far from the power plant. For MDA concentration, effect of different levels of industrial density was observed only at points close to the power station, probably because of higher levels of humidity near the power plant. For PI significantly higher values were observed in samples at points far from the power station and with high industrial density. This shows the additive effect of the principal emission sources that act on the response of P. subrudecta to air pollutants.     

a rapid emission survey procedure for industrial air pollutants

A methodology has been developed to calculate industrial air pollutant emissions with an absolute minimum of effort. The procedure is dependent upon available industrial fuel data for Standard Industrial Classifications for Standard Metropolitan Statistical Areas as published by the Census of Manufacturers. Emission factors were developed which include both combustion and process losses and six SIC classifications which consume, on the average, about 80 per cent of the industrial fuels in urban areas. In spite of the diversity of industrial processes which dictate the weight of emissions discharged from industrial operation, factors have been developed which are considered representative for urban areas across the nation. The development of such factors permits the calculation of industrial emissions with a minimum of man-hours. The developed procedure allows the calculation of industrial emissions on an urban basis, a state basis, or a nation basis.     

Identification of stationary sources of air pollutants by concentration statistical analysis

The atmospheric concentrations of benzene, toluene, ethylbenzene and isomeric xylenes (BTEX) in a medium-sized town (S. Maria Capua Vetere, about 32000 inhabitants, Southern Italy) have been determined during working days and weekends in 2006. The procedure used was 24h passive adsorption by samplers distributed throughout the town followed by GC/MS analysis. On a yearly base, the arithmetic mean benzene concentrations were above the limit required by the 2000/69/CE European Directive. The Pearson correlation coefficients of the 24h geometric mean BTEX concentrations were indicative of stationary sources of toluene located in a well circumscribed area of the urban territory, active only during the working days and not officially recognized. The results highlight the effectiveness of the statistical approach used in this study for the identification of pollutant sources.     

Codependencies of reactive air toxic and criteria pollutants on emission reductions

It is important to understand the effects of emission controls on concentrations of ozone, fine particulate matter (PM2.5), and hazardous air pollutants (HAPs) simultaneously, to evaluate the full range of health, ecosystem, and economic effects. Until recently, the capability to simultaneously evaluate interrelated atmospheric pollutants ("one atmosphere" analysis) was unavailable to air quality managers. In this work, we use an air quality model to examine the potential effect of three emission reductions on concentrations of ozone, PM2.5, and four important HAPs (formaldehyde, acetaldehyde, acrolein, and benzene) over a domain centered on Philadelphia for 12-day episodes in July and January 2001. Although NO(x) controls are predicted to benefit PM2.5 concentrations and sometimes benefit ozone, they have only a small effect on formaldehyde, slightly increase acetaldehyde and acrolein, and have no effect on benzene in the July episode. Concentrations of all pollutants except benzene increase slightly with NO(x) controls in the January simulation. Volatile organic compound controls alone are found to have a small effect on ozone and PM2.5, a less than linear effect on decreasing aldehydes, and an approximately linear effect on acrolein and benzene in summer, but a slightly larger than linear effect on aldehydes and acrolein in winter. These simulations indicate the difficulty in assessing how toxic air pollutants might respond to emission reductions aimed at decreasing criteria pollutants such as ozone and PM2.5.     

Hazardous air pollutants from mobile sources in the Metropolitan Area of Mexico City

Environmental agencies are currently in the process of implementing a new air management program, which includes the improvement of fuel quality. In this work, exhaust emissions data and estimated relative risk for various fuels testing in-use vehicles, equipped with three different exhaust emission control technologies, are presented. Aromatics, sulfur, and olefins contents; type of oxygenated compound; and Reid vapor pressure were varied. The aim also includes calculating the ozone (O3) forming potential and a relative cancer risk of emissions from current and formulated gasoline blends in Mexico. The proposed gasoline decreases carbon monoxide, total hydrocarbons (THC), and nitrogen oxides emissions by 18 and 14%, respectively, when compared with gasoline sold in the rest of the country and within ozone nonattainment metropolitan areas in Mexico, respectively.     

Investigation of carbonyl compounds in air from various industrial emission sources

The emission concentrations of carbonyl compounds in air were quantified from a total of 195 man-made source units within 77 individual companies at a large industrial complex in Korea. The measurement data were evaluated both by absolute magnitude of concentration and by their relative contribution to malodor formation such as malodor degree (MD) derived from empirical formula. It was found that formaldehyde exhibited the highest mean concentration of 323ppb with a median value of 28.2ppb, while butyraldehyde recorded the highest contribution to odor formation with an MD value of 3.5 (186 (mean) and 9.8ppb (median)). The relative intensity of carbonyl emission, when compared by the sum of MD, showed the highest source strength from the food and beverage (industry sector) and scrubber (source unit). A comprehensive evaluation of the carbonyl data from diverse industrial facilities thus allowed us to describe the fundamental patterns of their emission.     

沸腾炉大气污染物初始排放因子的研究

以20台沸腾炉(≤60MW)的燃料特性分析数据和大气污染物的排放实测数据为基础,研究了颗粒物(PM)、SO2和NOX初始排放因子EFP0M、EF0SO2、EF0NOX的变化规律,并利用SPSS13.0统计分析软件,分析了EFP0M、EFS0O2、EF0NOX与影响因子间的相关性。结果表明,在沸腾炉运行负荷≥80%的条件下,EF0PM基本不受锅炉出力(W)、燃煤灰分质量分数(Aar)及过量空气系数(α)的影响,EFP0M与W、Aar、α不具有相关性;EF0SO2主要受燃煤硫质量分数(Sar)的影响,两者具有显著正相关关系;W、α、燃煤干燥基挥发分质量分数(Vdaf)对EF0NOX具有显著影响,EF0NOX与α具有显著正相关关系,而EF0NOX与W、Vdaf具有显著负相关关系;EFS0O2和EF0NOX影响因子由强到弱的顺序为:①EFS0O2:SarαW;②EF0NOX:VdafαW燃煤氮质量分数(Nar)。     

Chemical composition of major VOC emission sources in the Seoul atmosphere

This paper describes a chemical analysis of volatile organic compounds (VOCs) for five emission sources in Seoul. The source categories included motor vehicle exhaust, gasoline evaporation, paint solvents, natural gas and liquefied petroleum gas (LPG). These sources were selected because they have been known to emit significant quantities of VOCs in the Seoul area (more than 5% of the total emission inventory). Chemical compositions of the five emission sources are presented for a group of 45 C2-C9 VOCs. Motor vehicle exhaust profiles were developed by conducting an urban tunnel study. These emissions profiles were distinguished from the other emission profiles by a high weight percentage of butanes over seasons and propane in the wintertime. It was found that this is due to the wide use of butane-fueled vehicles. To obtain gasoline vapor profiles, gasoline samples from five major brands for each season were selected. The brands were blended on the basis of the marketshare of these brands in Seoul area. Raoult's law was used to calculate gasoline evaporative compositions based on the liquid gasoline compositions. The measured and estimated gasoline vapor compositions were found to be in good agreement. Vehicle and gasoline evaporation profiles were made over seasons because of the seasonal change in their compositions. Paint solvent emissions profiles were produced based on a product-use survey and sales figures. These profiles are a composite of four major oil-based paints and thinning solvent. The source profile of natural gas was made on a methane-free basis. It was found that Ethane and propane were the most abundant compounds accounting for 95% of the natural gas composition. LPG was largely composed of propane and ethane and the remaining components were minor contributors.     

Emission of air pollutants from burning candles with different composition in indoor environments

Candle composition is expected to influence the air pollutants emissions, possibly leading to important differences in the emissions of volatile organic compounds and polycyclic aromatic hydrocarbons. In this regard, the purity of the raw materials and additives used can play a key role. Consequently, in this work emission factors for some polycyclic aromatic hydrocarbons, aromatic species, short-chain aldehydes and particulate matter have been determined for container candles constituted by different paraffin waxes burning in a test chamber. It has been found that wax quality strongly influences the air pollutant emissions. These results could be used, at least at a first glance, to foresee the expected pollutant concentration in a given indoor environment with respect to health safety standards, while the test chamber used for performing the reported results could be useful to estimate the emission factors of any other candle in an easy-to-build standardised environment.     

A study on the potential sources of air pollutants observed at Tjörn,Sweden

The Potential Source Contribution Function (PSCF) receptor model combines both chemical and meteorological information. In this study, PSCF was employed to identify the potential source emission regions for aerosol compositions measured at Tjörn, Sweden (58.01 °N, 11.36 °E). PSCF was for the first time applied on a European scale. One hundred and fifty-two four-day air parcel backward trajectories were combined with concentrations of sixteen elements determined in 33 coarse and fine aerosol samples. The observations were made between February 17 and March 26, 1985. The modeling results of the heavy metals V, Pb, Zn, and As are presented and compared with available emission inventory data. A number of known industrialized regions in the former USSR and Europe are found of high potential to be the emission source areas. These areas are in good agreement with the known emission information. The PSCF maps of total sulfur, Non-Seasalt-Sulfur (N.S.S.) and chlorine are also presented. High potential regions in the Arctic area exist in the PSCF map for total sulfur wheres they do not occur in that for N.S.S.     

Mercury emission trend influenced by stringent air pollutants regulation for coal-fired power plants in Korea

Regulatory control of mercury emission from anthropogenic sources has become a global concern in the recent past. Coal-fired power plants are one of the largest sources of anthropogenic mercury emission into the atmosphere. This paper summarizes the current reducing trend of mercury emission as co-beneficial effect by more stringent regulation changes to control primary air pollutants with introducing test results from the commercial coal-fired facilities and suggesting a guideline for future regulatory development in Korea. On average, mercury emission concentrations ranged 16.3–2.7 μg Sm^?3, 2.4–1.1 μg Sm^?3, 3.1–0.7 μg Sm^?3 from anthracite coal-fired power plants equipped with electrostatic precipitator (ESP), bituminous coal-fired power plants with ESP + flue gas desulphurization (FGD) and bituminous coal-fired power plants with selective catalytic reactor (SCR) + cold side (CS) ? ESP + wet FGD, respectively. Among the existing air pollution control devices, the best configuration for mercury removal in coal-fired power plants was SCR + CS ? ESP + wet FGD, which were installed due to the stringent regulation changes to control primary air pollutants emission such as SO₂, NOx and dust. It was estimated that uncontrolled and controlled mercury emission from coal-fired power plants as 10.3 ton yr^?1 and 3.2 ton yr^?1 respectively. After the installation of ESP, FGD and SCR system, following the enforcement of the stringent regulation, 7.1 ton yr^?1 of mercury emission has been reduced (nearly 69%) from coal-fired power plants as a co-benefit control. Based on the overall study, a sample guideline including emission limits were suggested which will be applied to develop a countermeasure for controlling mercury emission from coal-fired power plants.     

Removal of phenolic estrogen pollutants from different sources of water using molecularly imprinted polymeric microspheres

The efficiency and effects of using Bisphenol A-molecularly imprinted polymeric microspheres (MIPMs) to remove phenolic estrogens from different sources of water were evaluated. MIPMs prepared by precipitation polymerization removed a group of phenolic estrogens from different kinds of water selectively and effectively. The highest removal efficiency was observed at pH=5. Fifty millimoles per litre ions or 10mg/L humid acid improved removal efficiency. MIPMs were more suitable to remove trace estrogens in large volume than high concentration of estrogens in small volume. The removal efficiency of spiked tap water, lake water and river water were better than that of distilled water. Hundred milligrams of MIPMs had higher removal selectivity and efficiency than those of 100mg or 300mg activated carbons. Moreover, MIPMs can be re-used for at least 30 times without losing any removal efficiency. MIPMs provided a selective, simple, reliable and practicable solution to remove trace phenolic estrogens from different sources of water.     

Comparison between the accumulation capacity of four lichen species transplanted to a urban site

The capacity to accumulate trace elements from the atmosphere of the lichens Hypogymnia physodes, Parmelia sulcata, Pseudevernia furfuracea and Usnea gr. hirta transplanted to an urban site of N Italy was compared. Twenty-nine elements (Al, As, Br, Ca, Cd, Ce, Cl, Co, Cr, Cs, Cu, Fe, Hg, I, K, La, Mg, Mn, Ni, Pb, Rb, Sb, Sc, Se, Sm, Th, Ti, V, Zn) were analyzed by Instrumental Neutron Activation Analysis (INAA) and Electro-Thermal Atomic Absorption Spectroscopy (ET-AAS). The ratio between the concentrations of each element in exposed samples to that of control samples (exposed-to-control ratio and EC ratio) was used to investigate the accumulation rates of lichen thalli. The results showed that in general elements did not exhibit well defined trends, but rather showed fluctuations, and indicated that H. physodes, P. furfuracea and U. gr. hirta have a similar accumulation capacity, while that of P. sulcata is lower.     

Photochemical ozone creation potentials (POCPs) for different emission sources of organic compounds under European conditions estimated with a Master Chemical Mechanism

Through the combined application of a speciated VOC emission inventory and an explicit chemical mechanism, a picture has been put together of the different contributions to photochemical ozone formation from 248 VOC emission source categories. The study has shown that the different VOC emission source categories show vastly different propensities for forming photochemical ozone as indexed by their photochemical ozone creation potentials (POCPs). POCPs range from close to zero for numerous processes, including halocarbon solvent usage, through to over 70 for diesel combustion and some reactive solvent and other product usage applications. The consequences of the large range in POCPs are highlighted for cost-effective VOC emission control strategies across north west Europe.     

Relationships between emission sources and air mass characteristics in East Asia during the TRACE-P period

Long-range transport of pollutants influenced by anthropogenic and natural emission sources in East Asia is investigated by using backward trajectory analysis along the NASA TRACE-P flight tracks and a numerical simulation with the three-dimensional chemical transport model (STEM-2k1). Observation-based regional distributions of trace gases are reconstructed using the observations obtained by measurements on board the DC-8 and P3-B aircrafts. Systematic features of the spatial distribution for each species are identified. It is found that the observed concentrations of CO and some NMHCs, and the ratios between these species, are highly associated with the source distribution features and their regional characteristics. Reconstructed fields of the observed and modeled ethane/CO and ethane/propane are found to reproduce well the estimated emission ratios in East Asia. We also investigated the time rate of change of the concentration of species and their ratio along the trajectory. From this analysis the propane/ethane and propane/acetylene ratios are shown to preserve their emission ratios during regional transport. However systematic differences in the propane vs. acetylene/CO relationships are found between the model and observation values. This analysis suggests that further efforts are needed to improve the estimates of biomass burning emissions in SE Asia. The results presented in this paper also suggest ways to further extend the capabilities to derive observation-based inventories.