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1.
Introduction This study collected long-term airborne lead concentrations in the Korean peninsula and analyzed their temporal, spatial, and cancer risk characterization. Methods Approximately, 12,000 airborne samples of total suspended particulate (TSP) were collected from 30 ambient air monitoring stations in inland (Daegu, Daejeon, Gwangju, and Seoul) cities and portal cities (Incheon, Busan, and Ulsan) over a period of 7?years (2004?C2010). High volume air samplers were employed to collect daily TSP samples during the second week of the consecutive months throughout the entire study period. The concentrations of Pb extracted from the TSP samples were analyzed using either inductively coupled plasma-atomic emission or flame atomic absorption spectrometry. Results The long-term high mean Pb concentrations were observed in the port cities including Incheon (88?±?18?ng/m 3), Ulsan (61?±?7?ng/m 3), and Busan (58?±?6?ng/m 3). In the temporal analysis, seasonal mean Pb levels were relatively higher in winter and spring than those in summer and fall. In the spatial analysis, the mean Pb levels in spring, winter, and fall from Incheon, which showed the highest seasonal concentrations except summer, were 110?±?19, 101?±?18, and 76?±?23?ng/m 3, respectively. In summer, the highest seasonal mean Pb level was observed in the largest industrial city and the second port city, Ulsan (78?±?15?ng/m 3), followed by Incheon (65?±?13?ng/m 3). Conclusion The estimated excess cancer risk analysis showed that inhalation of Pb could result in cancer for one or two persons per million of population in the Korean peninsula. 相似文献
2.
Contribution of pollution from different types of sources in Jamshedpur, the steel city of India, has been estimated in winter 1993 using two approaches in order to delineate and prioritize air quality management strategies for the development of region in an environmental friendly manner. The first approach mainly aims at preparation of a comprehensive emission inventory and estimation of spatial distribution of pollution loads in terms of SO 2 and NO 2 from different types of industrial, domestic and vehicular sources in the region. The results indicate that industrial sources account for 77% and 68% of the total emissions of SO 2 and NO 2, respectively, in the region, whereas vehicular emissions contributed to about 28% of the total NO 2 emissions. In the second approach, contribution of these sources to ambient air quality levels to which the people are exposed to, was assessed through air pollution dispersion modelling. Ambient concentration levels of SO 2 and NO 2 have been predicted in winter season using the ISCST3 model. The analysis indicates that emissions from industrial sources are responsible for more than 50% of the total SO 2 and NO 2 concentration levels. Vehicular activities contributed to about 40% of NO 2 pollution and domestic fuel combustion contributed to about 38% of SO 2 pollution. Predicted 24-h concentrations were compared with measured concentrations at 11 ambient air monitoring stations and good agreement was noted between the two values. In-depth zone-wise analysis of the above indicates that for effective air quality management, industrial source emissions should be given highest priority, followed by vehicular and domestic sources in Jamshedpur region. 相似文献
3.
The composition of ambient air pollution, emphasising the ambient particulate matter, has been investigated for 14 wintertime smog periods (SO 2 and/or suspended particulate concentrations exceeding 400 μg m −3) in Berlin (West). The total aerosol mass concentration, the SO 2, CO, NO and NO 2 and pertinent meteorological parameters were measured. For chemical characterization the aerosol was collected by hi-volume, low-volume samplers and cascade impactors. The samples were analysed for the metals Pb, Cd, Mn, Ni; the water soluble ions: NH 4+, SO 42−, NO 3−; and the PAH's: Fl, Py, Per, BaP, BghiP and Cor. The aerosol size distribution (0,01 < dp < 20 μm) was measured by a combination of electrical and optical analysers with a time resolution of 10 min.The smog periods lasted from 6 to 100 h and occured during anticyclonic conditions with restricted vertical mixing and low to moderate wind velocities. The smog producing pollutants originated either in the city of Berlin or in the industrial regions 100–200 km away.Ambient air quality standards were exceeded by SO 2 (highest 24-h concentration: 760 μg m −3), NO x (320), TSP (930) and SO 42− (190). BaP levels of up to 92 μg m −3 were measured. The total sulfate level increases with the SO 2 concentration and exceeds 100 μg m −3 for SO 2 levels above 600 μg m −3. In 40% of all cases the aerosol sulfate seems to be more acidic than (NH 4)HSO 4. The secondary aerosol fraction, i.e. the sum of SO 42−, NH 4+ and NO 2− ranges from 23 up to 65% of TSP and is related to the age of the pollutants.The composition of the pollutants reflects the different emission patterns of the various source regions and chemical conversions during the trip from the sources to the measuring station. Therefore, the patterns of the composition of the pollutants provide a means to apportion the pollutants among contributing source regions. Thus, it seems possible to develop a scheme to determine during an ongoing smog condition the major contributing source region on the basis of real time measurements of selected physical and chemical parameters of ambient pollutants. 相似文献
4.
Pulmonary function of approximately 200 school children in Steubenville, OH was measured before and immediately following air pollution alerts in the fall of 1978 and 1979. TSP concentrations exceeded the National Primary Ambient Air Quality 24 h standards in 1978. SO 2 exceeded the standard in 1979. The children were then reexamined in three weekly visits following each alert. Estimated mean Forced Vital Capacity (FVC) was approximately 2% lower following each alert, although the lowest means were observed one to two weeks after the episodes. Forced Expired Volume in 0.75 sec (FEV 0.75) did not change during the 1978 study, but was 4% lower immediately following the 1979 alert. The children were measured again in five weekly examinations in the spring and fall of 1980. Air pollution levels did not exceed the standards on either occasion. In the spring of 1980, estimated mean FVC and FEV 0.75 showed a decline similar to that observed following the alerts in 1978 and 1979. In the fall of 1980, there were no significant differences in the estimated mean FVC or FEV 0.75 between the examinations. A total of 335 children were tested in the four studies, including 194 who participated in more than one study. The evidence for each child from all the studies was combined in a regression analysis of pulmonary function on TSP and SO 2 average concentrations in the previous 24 h. The distribution of the individual regression coefficients was centered significantly below zero, implying a decrease in pulmonary function with increasing TSP and SO 2 concentrations. The magnitude of the median change was less than 1% of the mean FVC and FEV 0.75 over the range of TSP and SO 2 concentrations observed. 相似文献
5.
The purpose of this study was to analyze quantitative relationships between air pollution and mortality, and to examine the impact of migration on pollution-related mortality functions. Dose-response functions were estimated for intra-urban variations in ambient air quality for the city of Jacksonville, Florida. Indices of air pollution used in this study were sulfur dioxide (SO 2) and total suspended particulates (TSP). Ambient air quality was measured by the dispersion of TSP and SO 2 across census tracts using the SYMAP dispersion model in conjunction with air quality monitoring stations. Holding other things constant, TSP apeared to have no statistically significant association with mortality rates. By contrast, the significance of the estimated coefficient for the pollution variable, SO 2, supported the contention that there is a positive and statistically significant relationship between air pollution and mortality rates. However, after making a limited test of the impact of migration on dose-response functions, the SO 2 pollution variable was no longer statistically significant. That is, recent migrants may have limited exposure to the existing level of SO 2 in Jacksonville, Florida, but carry with them long term exposure to more heavily polluted areas in the Northern United States. The results of this study suggest that further epidemiological studies and economic analysis of the health effects on air pollution should make some attempt to control the migration effect. 相似文献
6.
Purpose This study presents a procedure to differentiate the local and remote sources of particulate-bound polycyclic aromatic hydrocarbons (PAHs). Methods Data were collected during an extended PM 2.5 sampling campaign (2009?C2010) carried out for 1?year in Venice-Mestre, Italy, at three stations with different emissive scenarios: urban, industrial, and semirural background. Diagnostic ratios and factor analysis were initially applied to point out the most probable sources. In a second step, the areal distribution of the identified sources was studied by applying the discriminant analysis on factor scores. Third, samples collected in days with similar atmospheric circulation patterns were grouped using a cluster analysis on wind data. Local contributions to PM 2.5 and PAHs were then assessed by interpreting cluster results with chemical data. Results Results evidenced that significantly lower levels of PM 2.5 and PAHs were found when faster winds changed air masses, whereas in presence of scarce ventilation, locally emitted pollutants were trapped and concentrations increased. This way, an estimation of pollutant loads due to local sources can be derived from data collected in days with similar wind patterns. Long-range contributions were detected by a cluster analysis on the air mass back-trajectories. Results revealed that PM 2.5 concentrations were relatively high when air masses had passed over the Po Valley. However, external sources do not significantly contribute to the PAHs load. Conclusions The proposed procedure can be applied to other environments with minor modifications, and the obtained information can be useful to design local and national air pollution control strategies. 相似文献
7.
Three thousand four hundred fifty-one Austrian elementary school children were examined (between 2 and 8 times) by spirometry by standardized methods, over a 5 yr period. The districts where they lived were grouped into those where NO 2 declined during this period (by at least 30 μg/m 3 measured as half year means) and those with less or no decline in ambient NO 2. In both groups of districts, SO 2 and TSP fell by similar amounts over this period. A continuous improvement of MEF25 (maximum exspiratory flow rate at 25% vital capacity) was found in districts with declining ambient NO 2. Populations did not differ in respect of anthropometric factors, passive smoking or socioeconomic status. A birth cohort from this study population which was followed up to age 18 confirmed the improved growth of MEF25 with decline in NO 2, while the improved growth of forced vital capacity was more related to decline in SO 2. This study provides the first evidence that improvements in the outdoor air quality during the 1980s are correlated with health benefits, and suggest that adverse effects on lung function related to ambient air pollution are reversible before adulthood. Improvement of small airway functions appeared to be more dependent on reductions of NO 2 than reduction in SO 2 and TSP. 相似文献
8.
The TSP, SO 4= and Pb levels observed downwind of a large refinery and in the city of Willemstad in Curaçao are presented. The results show that wiht increasing wind speed TSP and SO 4= levels increase while Pb levels decrease. On the other hand, at relatively constant wind speeds a good correlation between TSP and Pb was observed.The correlation observed between TSP, SO 4= and Pb and the wind speed, the effect of rain on the atmospheric levels observed during the sampling period, the lack of secondary pollutants (e.g. ozone, NO 3?) and the composition of the island background air, allow us to conclude that the SO 4= measured at the monitoring sites is mainly produced as a primary pollutant in the refinery, the high atmospheric TSP levels are due to refinery emissions (traditional source) and the recirculation of street dust particles (non traditional source) produced by traffic and the predominantly high wind velocity.The implication on air quality and control measures are discussed. 相似文献
9.
Covid-19 lockdowns have improved the ambient air quality across the world via reduced air pollutant levels. This article aims to investigate the effect of the partial lockdown on the main ambient air pollutants and their elemental concentrations bound to PM2.5 in Hanoi. In addition to the PM2.5 samples collected at three urban sites in Hanoi, the daily PM2.5, NO2, O3, and SO2 levels were collected from the automatic ambient air quality monitoring station at Nguyen Van Cu street to analyze the pollution level before (March 10th–March 31st) and during the partial lockdown (April 1st–April 22nd) with “current” data obtained in 2020 and “historical” data obtained in 2014, 2016, and 2017. The results showed that NO2, PM2.5, O3, and SO2 concentrations obtained from the automatic ambient air quality monitoring station were reduced by 75.8, 55.9, 21.4, and 60.7%, respectively, compared with historical data. Besides, the concentration of PM2.5 at sampling sites declined by 41.8% during the partial lockdown. Furthermore, there was a drastic negative relationship between the boundary layer height (BLH) and the daily mean PM2.5 in Hanoi. The concentrations of Cd, Se, As, Sr, Ba, Cu, Mn, Pb, K, Zn, Ca, Al, and Mg during the partial lockdown were lower than those before the partial lockdown. The results of enrichment factor (EF) values and principal component analysis (PCA) concluded that trace elements in PM2.5 before the partial lockdown were more affected by industrial activities than those during the partial lockdown. 相似文献
10.
A detailed physical and chemical characterisation of total suspended particles (TSP) in the highly industrialised city of Huelva (southwestern Spain) was carried out. The results evidenced a coarse grain-size prevalence (PM 10 accounting for only 40% of TSP mass, 37 and 91 μg/m 3, respectively). PM 10 levels are in the usual range for urban background sites in Spain. The crustal, anthropogenic and marine components accounted for a mean of a 40%, 24% and 5% of bulk TSP, respectively. As expected from the industrial activities, relatively high PO 43− and As levels for an urban site were detected. In addition to the crustal and marine components, source apportionment analysis revealed three additional emission sources influencing the levels and composition of TSP: (a) a petrochemical source, (b) a mixed metallurgical-phosphate source, (c) and an unknown source (Sb and NO 3−).Due to the high local emissions, the mean TSP anthropogenic contribution (mostly PM 10) obtained for all possible air mass transport scenarios reached 18–29 μg/m 3. The 2010 annual EU PM 10 limit value (20 μg/m 3) would be exceeded by the anthropogenic load recorded for all the air mass transport scenarios, with the exception of the North Atlantic transport (only 15% of the sampling days). Under African air mass transport scenarios (20% of sampling days), the TSP crustal contribution reached near three times the local crustal contribution. It must be pointed out that this crustal input should diminish when sampling PM 10 due to the dominant coarse size distribution of this type of particles. 相似文献
11.
Whereas most estimates of material damage are based on industrial surveys, the estimates produced in this study were derived from material damage experiments and ambient air quality data. Air quality data on SO 2 were obtained from 200 or more monitoring sites primarily located in heavily populated or polluted areas. Material threshold damage function data were then compared with SO 2 levels, and an estimate of losses, as reflected in increased maintenance and replacement costs, was determined. Estimates of the total stock of various materials in use were derived from census and industry data and allocated geographically according to population. A substantial decrease in the ambient SO 2 levels, particularly in larger urban areas, has occurred during the past five years. From 1968 to 1972, the estimated amount of material damage from SO 2 in the U. S. decreased from $900 million/yr to less than $100 million. During this period, the estimated percentage of man made materials exposed to SO 2 levels exceeding the proposed secondary annual average standard (60 μg/m 3) and primary annual average standard (80 μg/m 3) in the U. S. fell respectively, from 20% to less than 5% and from more than 10% to less than 1%. Most of the present loss is attributed to corrosion damage of metallic surfaces that are normally exposed to the ambient environment. 相似文献
12.
As part of an environmental impact assessment for building a new town in Junk Bay, continuous measurement of SO 2 and particulate concentrations was carried out from October 1981 to June 1982 at three sites in Junk Bay to study the air quality in the area. Flame photometric SO 2 analyzers were used to measure ambient SO 2 level, whereas tape monitors were used to measure the ambient suspended particulate level (in terms of soiling index, or coefficient of haze per 1000 feet). It was found that the mean SO 2 concentrations at the three monitoring sites ranged from 5μg m −3 to 35μg m −3. Maximum daily values up to about 250 μg m −3 and hourly values up to 800 μg m −3 had been recorded on occasion. Comparison of the hourly meteorological data and the hourly SO 2 concentrations in four high-SO 2-level days suggested that the ‘sulfur dioxide episodes’ were all associated with very light wind speeds and local sources. The mean coefficient of haze level in Junk Bay was less than one, which corresponded to very slight particulate pollution. 相似文献
13.
The trends in and relationships between ambient air concentrations of sulfur dioxide and sulfate aerosols at 48 urban sites and 27 nonurban sites throughout the U.S. between 1963 and 1972 have been analyzed. The substantial decreases in ambient SO 2 concentrations measured at urban sites in the eastern and midwestern U.S. are consistent with the corresponding reductions in local SO 2 emissions, but these decreases have been accompanied by only modest decreases in ambient sulfate concentrations. Large differences in the amounts of SO 2 emitted within individual air quality control regions are associated with much smaller differences in the corresponding ambient sulfate concentrations. Substantial changes in the patterns of SO 2 emissions between air quality regions result in essentially no differences between ambient sulfate concentrations in those air quality regions. Comparisons of several air quality regions in the eastern and western U.S. with similar SO 2 emission levels and patterns of emissions clearly demonstrates the higher ambient sulfate concentration levels in eastern air quality control regions. Relationships between SO 2, sulfates, and vanadium concentrations at eastern nonurban U.S. sites cannot be explained by local emission sources. These various observed results can be best explained by long distance sulfur oxide transport with chemical conversion of SO 2 to sulfates occurring over ranges of hundreds of kilometers. This conclusion has been suggested earlier and the present analysis strongly supports previous discussions. An impact of long range transport of sulfates is to emphasize the need for Consistent strategies for reduction of sulfur oxides throughout large geographical regions. Additions of large capacities involving elevated sources in mid-continental or western regions could result in significant increases in sulfate concentrations well downwind of such sources. Some of the types of research activities required to quantitate crucial experimental parameters are discussed. 相似文献
14.
The computer model Industrial Source Complex Short Term (ISCST) was used to study the stack emissions from a refuse Incinerator proposed for the island of Bermuda. The model predicts that the highest ground level pollutant concentrations will occur near Prospect, 800 m to 1000 m due south of the stack. We installed a portable laboratory and instruments at Prospect to begin making air quality baseline measurements. By comparing the model’s estimates of the incinerator contribution to the background levels measured at the site we predict that stack emissions will not cause an Increase In TSP or SO 2. The incinerator will be a significant source of HCI to Bermuda air with ambient levels approaching air quality guidelines. 相似文献
15.
Real-time chemical measurements have been made as part of a field study of air quality in the city and harbour of Cork, Ireland. The data relate to the year 2008, with particular attention paid to the period between May and August. Eight air quality parameters were measured: NO, O 3, NO 2, SO 2, EC, OC, particulate SO 42? and PM 2.5. The data have been used in a novel way involving wind and temporal averaging, along with Principal Component Analysis (PCA) and Positive Matrix Factorisation (PMF) methodologies to extrapolate major source contributions for PM 2.5. It is demonstrated that continuous monitoring of standard air quality parameters, such as NO, NO 2, SO 2, along with EC, OC and particulate SO 42?, can be used to provide relevant, cost-effective initial estimates of source contributions to ambient PM 2.5 levels. It is also shown that the benefit of including OC and particulate SO 42? in the monitoring protocol is considerable. Three major source groups of ambient PM 2.5 mass in Cork were identified and quantified using this combined monitoring and modelling approach; road transport (19%), domestic solid fuel burning (14%) and oil-fired domestic and industrial boilers, including power generation plants (31%). 相似文献
16.
A long-term study of measurement of concentration of NO x, SO 2 and TSP pollutants have been done in a port and harbour region in India. Monthly measurements of gaseous and particulate pollutants were made at six monitoring stations from January 1997 to December 2000. Meteorological data was also simultaneously collected. In this study, the relationship between monitored ambient air quality data and meteorological factors, such as wind speed, temperature, is statistically analysed, using the SPSS package. The monthly mean concentrations of NO x, SO 2 and TSP were in the range of 19.5–59.0 μg/m3, 8.6–51.3 μg/m3 and 88.2–199.3 μg/m3, respectively. The results show that TSP is strongly correlated with NO x and SO 2 with a correlation coefficient of 0.83 and 0.82, respectively. The correlation coefficients for TSP, NO x, and SO 2 with wind are –0.78, –0.78, and –0.88, respectively. 相似文献
17.
A method is described for quantifying health risks to asthmatics briefly exposed to elevated levels of SO 2. By combining symptomologlcal and physiological measurements, we have developed a dose-response surface that relates both severity and incidence of response to ambient air quality levels. The complete model to assess potentially avoidable risks includes power plant emission data; ambient SO 2 background levels; demographic and activity patterns of asthmatics, the identified population at risk; and the dose-response surface. The estimated annual risk to persons experiencing an SO 2-lnduced response due to a nearby power plant is quite small (response rates under 3 percent). Uncertainties due to modeling errors, variations in activity patterns, demographics and physiological response are discussed. 相似文献
18.
Introduction Trends in precipitation pH and conductivity during 1992?C2009, and in ionic compositions from January 2007 to June 2009, are reported from Lushan Mountain, one of the highest mountains in mid-east China. Annual mean pH was in the range of 4.35?C5.01 and showed a statistically very significant ( P?0.01) decreasing trend with time. Annual mean conductivity showed a statistically significant ( P?0.05) increasing trend, although this was not the case for non-H conductivity. Increasing rainwater acidity was mainly caused by increasing amounts of acid substances entering the rain. The trends in precipitation pH and conductivity were directly associated with energy consumption. Results and discussions Over the period of study, Lushan Mountain received more rainfall in spring and summer. The pH values varied seasonally with winter minima. The winter multiyear seasonal mean pH was 4.35. The corresponding summer value was 4.88. SO 4 2? and NO 3 ? were the main anions, and NH 4 + and Ca 2+ the main cations. The anion to cation ratio was 0.8?C1.0, and that of [SO 4 2? ] to [NO 3 ? ] was 2.4-3.0, much lower than that of the 1980s. However, sulfuric acid was still the main acid present. The ratio of [NH 4 + ] to [Ca 2+] was about 1.0, suggesting that these two alkaline substances provided close acid neutralizing capacity. The ratio of [Cl ?] to [Na +] was about 0.67, somewhat lower than that of natural precipitation. Conclusions Ionic composition varied seasonally and was closely correlated to the amounts of rainfall and pollution. Trajectory analyses showed that the trajectories to Lushan Mountain could be classified in six clusters and trajectories originating from the South Sea and the areas surrounding Lushan Mountain had the greatest impacts on precipitation chemistry. 相似文献
19.
Map Ta Phut industrial area (MA) is the largest industrial complex in Thailand. There has been concern about many air pollutants over this area. Air quality management for the area is known to be difficult, due to lack of understanding of how emissions from different sources or sectors (e.g., industrial, power plant, transportation, and residential) contribute to air quality degradation in the area. In this study, a dispersion study of NO 2 and SO 2 was conducted using the AERMOD model. The area-specific emission inventories of NO x and SO 2 were prepared, including both stack and nonstack sources, and divided into 11 emission groups. Annual simulations were performed for the year 2006. Modeled concentrations were evaluated with observations. Underestimation of both pollutants was found, and stack emission estimates were scaled to improve the modeled results before quantifying relative roles of individual emission groups to ambient concentration over four selected impacted areas (two are residential and the others are highly industrialized). Two concentration measures (i.e., annual average area-wide concentration or AC, and area-wide robust highest concentration or AR) were used to aggregately represent mean and high-end concentrations for each individual area, respectively. For AC-NO 2, on-road mobile emissions were found to be the largest contributor in the two residential areas (36–38% of total AC-NO 2), while petrochemical-industry emissions play the most important role in the two industrialized areas (34–51%). For AR-NO 2, biomass burning has the most influence in all impacted areas (>90%) except for one residential area where on-road mobile is the largest (75%). For AC-SO 2, the petrochemical industry contributes most in all impacted areas (38–56%). For AR-SO 2, the results vary. Since the petrochemical industry was often identified as the major contributor despite not being the largest emitter, air quality workers should pay special attention to this emission group when managing air quality for the MA. Implications: Effective air quality management in Map Ta Phut Industrial Area, Thailand requires better understanding of how emissions from various sources contribute to the degradation of ambient air quality. Based on the dispersion study here, petrochemical industry was generally identified as the major contributor to ambient NO 2 and SO 2. By accounting for all stack and non-stack sources, on-road mobile emissions were found to be important in some particular areas. 相似文献
20.
Purpose The study examines the effectiveness of red mud, blast furnace (BF) slag, and alum-derived water treatment sludge as immobilizing agents for excessive soluble P that had accumulated in three green waste-based composts. Methods The three wastes were applied at 0%, 5%, 10%, and 20% w/ w to three different composts, all containing extremely high concentrations of extractable P, and were incubated for 60?days. Water-soluble P was measured regularly throughout the incubation period, and at the end, P extractable with resin, 0.05?M NaHCO 3, and 0.005?M H 2SO 4 were also measured. Results In the water extracts, inorganic P made up more than 85% of the total P present. All three materials had the ability to adsorb P and thus lowered water-soluble P concentrations. Water treatment sludge was clearly the most effective material, and this was attributed to its amorphous nature (thus, large Brunauer?CEmmett?CTeller surface area) and its acid pH (6.8) compared with the alkaline pH (10?C11) of the other two materials. Water treatment sludge was also the most effective at lowering resin- and NaHCO 3-extractable P. When H 2SO 4 was used as the extractant, BF slag tended to be the most effective material at lowering extractable P, followed by water treatment sludge, and red mud. That is, the P immobilized by water treatment sludge was extractable with acid but not with water, resin, or NaHCO 3. Conclusions Water treatment sludge has the potential to be used as an effective immobilizing agent for soluble P in composts, and it should be trialed under field conditions. 相似文献
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