International field intercomparison measurements of atmospheric mercury species at Mace Head,Ireland

Eleven laboratories from North America and Europe met at Mace Head, Ireland for the period 11–15 September 1995 for the first international field intercomparison of measurement techniques for atmospheric mercury species in ambient air and precipitation at a marine background location. Different manual methods for the sampling and analysis of total gaseous mercury (TGM) on gold and silver traps were compared with each other and with new automated analyzers. Additionally, particulate-phase mercury (Hg_part) in ambient air, total mercury, reactive mercury and methylmercury in precipitation were analyzed by some of the participating laboratories. Whereas measured concentrations of TGM and of total mercury in precipitation show good agreement between the participating laboratories, results for airborne particulate-phase mercury show much higher differences. Two laboratories measured inorganic oxidized gaseous mercury species (IOGM), and obtained levels in the low picogram m^-3 range.     

Interlaboratory exercises for volatile organic compound determination

The results of a European level intercomparison involving measurements of 26 hydrocarbons (from C2 to C9) at ambient air concentration level are discussed. On-line sampling with cryo-GC-FID analysis was the most commonly used methodology among the 20 participating laboratories. The stability of the gas samples in the canisters; the calibration methodology, the separation of peaks and the low level of concentrations were identified as the most important factors, which contributed to the increase in the uncertainty of the measurement. Uncertainty values associated with the common method used for the quantification of each compound and exercise were also determined.     

A High Volume Stack Sampler

This paper deals with the development design, and trial application of a sampling train to gather a relatively large amount of particulate sample in a short period of time. With air pollution sources installing control equipment to reduce emissions to the required low levels, it becomes necessary to use a sampling device which can collect a representative sample in a reasonable period of time. Some of the sampling trains currently being specified are expensive, awkward, and nearly impossible to use under field conditions. The high-volume train overcomes ail of these shortcomings and has some additional advantages. It uses the same glass fiber filter that is specified for ambient air particulate sampling so the emission test results are directly comparable to ambient air sampling data. The laboratories currently weighing and analyzing the glass filters need no additional equipment for the emission sampling analysis. The sample collected by the high-volume probe may be analyzed microscopically for size and characteristics of the particles. This is very important if control equipment is to be specified for the process or source. The high-volume sampler was evaluated on field tests of wood fired boilers, incinerators, wigwam burners, asphalt batching plants, seed cleaning plants, and wood fiber filtration systems. The results of several typical tests using the sampler on these sources are included in the paper.     

Levels of PCDD/FS in ambient air and soil in the vicinity of a municipal solid waste incinerator in Hsinchu

Levels of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) were determined in twenty-one ambient air samples, eight soil samples and two stack gas samples, collected near or in a municipal solid waste incinerator (MSWI) in Hsinchu, Taiwan. A systematic decrease of PCDD/Fs in the ambient air from the northeastern area was observed. PCDD/Fs levels measured in the ambient air range from 0.058 to 0.127 pg-TEQ/m3. Higher PCDD/Fs levels in the ambient air were found during winter. In addition, PCDD/Fs levels measured in the soil range from 0.524 to 5.02 pg-TEQ/g d.m. Principal component analysis (PCA) and hierarchical cluster analysis (HCA) did not provide sufficient evidence that the environmental PCDD/Fs contamination was caused by emissions from the Hsinchu MSWI. An unknown PCDD/Fs source was proposed using congener profile analysis and supported by both PCA and HCA.     

Survey of Laboratory Performance Analysis of Simulated Ambient S02 Bubbler Samples

The Quality Control Branch of the Quality Assurance and Environmental Monitoring Laboratory, National Environmental Research Center, Research Triangle Park, N. C, coordinated a nationwide interlaboratory study which surveyed the ability of participating laboratories to analyze simulated ambient sulfur dioxide samples. The purposes of the study were (1) to provide participating laboratories with a means for self evaluation of their performance, and (2) to begin to acquire information which indicates the quality of ambient SO₂ data being reported.

Sample vials of sodium sulfite in mannitol were distributed to 134 laboratories throughout the country that routinely analyze for atmospheric SO₂. No restrictions were placed on the method of analysis other than that the normal absorbing solution used with the analysis be a tetrachloromercurate II solution. Each sample set contained five separate vials. Each vial, when mixed properly with absorbing reagent, simulated a 24 hour bubbler sample. The range of concentrations in each set extended from approximately the lower detectable limit of the pararosaniline method to approximately the alert level as described in Federal Regulations.     

Evaluation of PCDD/Fs patterns emitted from incinerator via direct ambient sampling and indirect serum levels assessment of Taiwanese

The aim of this study was to evaluate the PCDD/Fs patterns in ambient air based on data information emitted from incinerator generated from ambient air measurements and those in serum. Four circular zones, namely A, B, C, and D, were identified based on simulated ambient annual average PCDD/Fs concentrations, from a selected municipal waste incinerator. Sixteen ambient samples were taken from the 4 circular zones across 4-seasons. Eighty-nine volunteers were recruited according to the demographic distribution within each zone. PCDD/Fs profiles were documented both for air and serum samples collected. Comparing to the congener patterns from ambient air and serum samples, we found that OCDD, OCDF, 1,2,3,4,6,7,8-HpCDD, and 1,2,3,4,6,7,8-HpCDF were the predominant groups among 17 congeners from both the ambient air and serum sample. And, factor analysis showed the distribution patterns of PCDD/Fs from ambient air and serum samples are almost identical across different zones, except for congener patterns of serum samples from residents in zone C. In addition, the average PCDD/Fs level significantly reduced for about 10 folds than those of the other three seasons when the incinerator was shut down in one of sampling periods. We might conclude that ambient air exposure was the most important contributor to PCDD/Fs levels in ambient air but not the single in serum. Therefore, another or more powerful source, such as occupational exposure, dietary intake or the consumption of local food, should be further investigated at the same time.     

Effect of ambient ozone and acid mist on aphid development

The effect of ambient air with increased ozone concentrations and artificial acid mist on the population growth of two different aphid species was studied: Aphis fabae on Phaseolus vulgaris and Phyllaphis fagi on seedings of Fagus sylvatica. Whereas the ambient air inhibited growth of Aphis fabae, it stimulated population growth of Phyllaphis fagi. In Fagus, analysis of a phloem exudate revealed that the amino acid/sugar ratio was significantly increased by the ambient air compared to filtered air. In Phaseolus, no significant differences in amino acid or sugar content of the phloem exudate could be found. Acid mist inhibited population development in both aphid species; the strongest effect was observed in the first weeks after artificial infestation.     

Another Look at New York City’s Air Pollution Problem

An analysis of the ambient air quality in New York City over the past several years has been made. The various sources of the contaminants are identified and evaluated as to their effects on ambient air quality. Meteorological data have been analyzed to develop insight into the influence of weather conditions upon ground level pollution concentrations. The results of these analyses are employed to indicate the approaches that will be most effective in improving air quality.     

Evaluation of weather conditions for methyl bromide ambient air monitoring in Monterey, Santa Cruz, and Kern Counties in the year 2000

Weather condition is one of the most important factors affecting spatial and temporal distributions of air pollutants, especially for short-term air dispersion. Abnormal weather conditions might lead to higher or lower ambient air concentrations than they would be under normal weather conditions. Therefore, testing for normality of weather conditions during the air monitoring period is an essential step for evaluating ambient air monitoring results. In this paper, a distance method was used to select a most representative weather station from the available candidates. An array of meteorological elements were identified that affect air dispersion and transportation. A statistical method was used to determine whether the weather conditions during the air monitoring period were significantly different from that of previous years. Using methyl bromide ambient air monitoring as a case study, this paper documents the methods, procedures, and results of weather analysis for Monterey, Santa Cruz, and Kern Counties during ambient air monitoring periods for methyl bromide in the year 2000. With a few exceptions, the meteorological elements and atmospheric stability factors, such as wind speeds, wind directions, and stability classes, during the monitoring period were in the normal range. Although there were higher frequencies of stable atmospheric conditions in Monterey/Santa Cruz Counties than in Kern County, weather conditions during the monitoring period were not significantly different from normal local weather conditions of previous years. Consequently, the subchronic air concentrations observed during the ambient air monitoring periods for methyl bromide in the year 2000 was taken under typical weather conditions of those areas at that time of the year.     

A New Approach to Setting Vehicle Emission Standards

Urban ambient air quality trend analysis was evaluated as an alternative to rollback analysis to estimate vehicle emission standards needed to achieve national ambient air quality standards. Examination of the trends of monthly maximum 8 hour average carbon monoxide concentrations, central business district traffic activity, and emission rates from vehicles on the road suggests that the automotive exhaust emission standard for carbon monoxide derived in response to the requirements of the Clean Air Act Amendments of 1970 may be ten times too severe. The excessive stringency of the vehicle emission standard for carbon monoxide was confirmed by two different analyses of the correlation between annual mean carbon monoxide concentration and frequency of occurrence of carbon monoxide concentrations above the level of the 8-hour standard. One correlation analysis using all available CAMP data involved an empirical approach and the other assumed that carbon monoxide concentrations are described by the lognormal distribution. Based on the analysis of CAMP air quality data, a vehicle carbon monoxide emission standard of approximately 29 grams per mile appears adequate to meet the ambient air quality standard. The large difference between the results of this analysis and the 1976 Federal vehicle carbon monoxide emission standard indicates the advisability of applying this methodology to verification of the standards for hydrocarbons and oxides of nitrogen.     

The Need for Representative Ambient Air Carbon Monoxide Sampling

Recent investigations have indicated that ambient air CO measurements may not reflect population exposure to CO. The lack of correlation may be due to improper siting of CO instruments, improper interpretation of air quality data, or both. Studies of population carboxy-hemoglobin levels are evaluated and compared with ambient air data.,

No significant correlation was found between median population COHb levels and reductions in CO concentrations required to meet ambient air standards when calculations used to estimate reductions were based on the second highest 8 hour average. However, calculated reductions based on annual average concentrations and a trend analysis technique correlated significantly with COHb levels in five cities from which both CAMP and COHb data were available.

Studies to determine the nature of the relationship between ambient air CO concentrations and population COHb levels are needed. The differences between the Occupational Safety and Health Act Regulations and the National Ambient Air Standards for carbon monoxide should be scrutinized to determine if a redefinition of the standards or their applicability is warranted. A reevaluation of the controls necessary to make reductions in population COHb burden may be necessary.     

Collaborative Testing of Methods to Measure Air Pollutants II. The Non-Dispersive Infrared Method for Carbon Monoxide

The Methods Standardization Branch of the Environmental Protection Agency, National Environmental Research Center, has undertaken a program to standardize methods used in measuring air pollutants covered by the national primary and secondary air quality standards. This paper presents the results of a collaborative test of the method specified for carbon monoxide.

The test involved analysis of CO in air samples (in cylinders) by participating laboratories. Three concentrations, covering the range of the method which is, 0 to 58 mg/m³, were analyzed dry and humidified on each of three days by 15 collaborators. The method of analysis, nondispersive infrared spectrometry (NDIR), involved an NDIR instrument in combination with different procedures for eliminating water vapor interference. A statistical analysis of the data obtained produced the following results: 1. The checking limit for duplicates (replication error) is 0.5 mg/m³.

2. The repeatability (variation within a laboratory) is 1.6 mg/m³.

3. The reproducibility (variation between laboratories) varies nonlinearly with concentration; i.e., a minimum of 2.3 mg/m³ at a concentration of 20 mg/m³ and ranges as high as 4.3 mg/m³ in the concentration range of 0 to 58 mg/m³.

4. The reproducibility at the level of the national primary ambient air quality standard, 10 mg/m³-8-hour average, is 2.5 mg/m³ or 25%.

5. The minimum detectable sensitivity is estimated to be 0.3 mg/m³.

6. Compensation for water vapor interference is satisfactorily accomplished using drying agents and refrigeration methods. The use of narrow-band optical filters alone may not provide adequate compensation.

7. The accuracy obtained depends upon the availability of reliable calibration gases. Based on the results of this study, the method produces results that average 2.5% high.

Future papers will contain test results for methods to measure other air pollutants.     

Characteristic Study of Ambient Air Total Gaseous Mercury (TGM) Concentrations During Rainy and Non-Rainy Periods at a Traffic Site in Taiwan

This investigation studied the concentrations of ambient air total gaseous mercury (TGM) during the rainy periods at the Hung-Kuang traffic sampling site in central Taiwan from May 26 to June 16, 2014. The results were compared with those of a previous study for ambient air TGM during non-rainy daytime and nighttime periods at the Hung-Kuang traffic sampling site, which was conducted during March 21 to July 20, 2012. The observed mean concentration of ambient air TGM was 1.16 ng/m³ during the rainy periods at the Hung-Kuang traffic sampling site. The mean ambient air TGM concentrations were higher in the non-rainy sampling period in daytime than in the rainy sampling period from this study. The mean ratio of non-rainy sampling period in daytime to that of rainy sampling period for ambient air TGM were 3.15. Furthermore, the mean ambient air TGM concentrations were higher in the non-rainy sampling period in nighttime in than in the rainy sampling period for this study. The mean rations for non-rainy sampling period in nighttime to that of the rainy sampling period for ambient air TGM were 2.70. The results obtained in this study also revealed that the ambient air TGM concentrations during the rainy period had the lowest concentrations when compared with the other sampling sites in other world regions.     

Ambient air monitoring of PCDD/Fs and co-PCBs in Gyeonggi-do, Korea

We started the monitoring for PCDD/Fs in ambient air and soil in August 2001, and co-PCBs in January 2002. Decreasing of PCDD/Fs and co-PCBs levels in ambient air were observed. The higher PCDD/Fs levels were found in winter and lower in autumn. We found that the industrial incinerators influenced the PCDD/Fs levels in ambient air. In the 2,3,7,8-substituted PCDD/Fs concentration profiles, the three major congeners occupied 67% of the total mass. In case of co-PCBs, PCB#118, #105 and #77 were observed as the main congeners. Five cluster groups discriminated by ratio of four components, O(8)CDD, 1,2,3,4,6,7,8-H(7)CDD, 1,2,3,4,6,7,8-H(7)CDF and O(8)CDF, were obtained from HCA (hierarchical cluster analysis).     

Long-term monitoring and modeling of polychlorinated dibenzo-p-dioxins and dibenzofurans from municipal solid waste incinerators and surrounding area in northern Taiwan

Municipal solid waste incinerators (MSWIs) have long been the major contributors of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) to ambient air in Taiwan. After stringent MSWI emission standards were introduced in 2001, the long-term continuous monitoring of flue gas and ambient air quality became necessary to ensure the effectiveness of the related control strategies. Three MSWIs and the surrounding ambient air were investigated in the current study for PCDD/F characteristics during 2006 to 2011. The average concentrations in the flue gas ranged from 0.008?~?0.0488 ng I-TEQ/Nm³, which is much less than the emission standard in Taiwan (0.1 ng I-TEQ/Nm³) (I-TEQ is the abbreviation of International Toxic Equivalent). This led to extremely low levels in the ambient air, 0.0255 pg I-TEQ/Nm³, much less than the levels seen in most urban areas around the world. Additionally, the results obtained using the Industrial Source Complex Short-Term Dispersion Model (ISCST3) indicate that the PCDD/F contributions from the three MSWIs to the ambient air were only in the range from 0.164?~?0.723 %. Principal component analysis (PCA) showed that the PCDD/Fs in the air samples had very similar characteristics to those from mobile sources. The results thus show that stringent regulations have been an effective control strategy, especially for urban areas, such as Taipei City.     

环境空气质量自动监测站的管理与维护

随着工业化、城镇化的深入推进,二氧化硫、氮氧化物、烟粉尘和挥发性有机物等各类污染物排放到环境中,致使中国大气受到严重污染,给人体的健康、动植物的生长、发育和繁殖等带来负面的影响。为实时监测环境空气质量,建立环境空气质量自动监测站逐渐成为大气污染防治的主要手段。文中以环境空气质量自动监测站为研究对象,提出环境空气质量自动监测站管理与维护面临的问题,探讨相应的解决措施,以期为环境空气质量自动监测站的管理与维护提供参考依据。     

Spatial interpretation of ambient air quality for the territory of the Czech Republic

A method for spatial interpretation and visualisation of measured air quality data is presented that may serve as a tool for ambient air quality characterisation using the least possible number of factors. This method enables comparison of different areas in relative terms and has practical consequences in decision making and public information. The 1996 data for the Czech Republic was used as a database. According to my results, not a single universal indicator can fully describe the ambient air quality albeit the three factors identified as "ambient air pollution", "ground-level ozone" and "wet atmospheric deposition" which are recommended. These selected factors represent three different aspects of ambient air quality and its impact on receptors. For the above factors black and white charts are presented classifying the Czech Republic territory into five categories as to relative ambient air quality. The air quality picture differs for the respective factors considerably.     

Atmospheric concentrations of saturated and aromatic hydrocarbons around a Greek oil refinery

Petroleum refineries are large industrial installations that are responsible for the emission of several pollutants into the atmosphere. Hydrocarbons are among the most important air pollutants that are emitted by petroleum refineries, since they are involved in almost every refinery process. The ambient air concentrations of many saturated and aromatic hydrocarbons were measured in several sites around an oil refinery, near the city of Corinth in Greece, during 1997. At the same time several meteorological parameters were also recorded. The seasonal, diurnal and spatial variations of the ambient air concentrations of these hydrocarbons were investigated and analyzed. An estimation of the contribution of the refinery to the measured atmospheric levels of hydrocarbons was also performed. The ambient air mixing ratios of the saturated and aromatic hydrocarbons in a large area outside the refinery were generally low, in ppbv range, much lower than the ambient air quality standards or the ambient air concentrations in the two largest urban centers in Greece, Athens and Thessaloniki.     

Assessment of vehicular pollution in China

As the motor vehicle population in China continues to increase at an annual rate of approximately 15%, air pollution related to vehicular emissions has become the focus of attention, especially in large cities. There is an urgent need to identify the severity of this pollution in China. Based on an investigation into vehicle service characteristics, this study used a series of driving cycle tests of in-use Chinese motor vehicles for their emission factors in laboratories, which indicated that CO and HC emission factors are 5-10 times higher, and NOx 2-5 times higher, than levels in developed countries. The MOBILE5 model was adapted to the Chinese situation and used to calculate the emission of pollutants from motor vehicles. Results show that vehicle emission is concentrated in major cities, such as Beijing, Guangzhou, Shanghai, and Tianjin. Motor vehicle emissions contribute a significant proportion of pollutants in those cities, with contribution rates of CO and NOx greater than 80% and 40%, respectively, in Beijing and Guangzhou. Urban air quality is far worse than the national ambient air quality standard. In conclusion, although China has a relatively small number of motor vehicles, most of them are concentrated within metropolitan areas, and their emissions are closely related to urban air pollution problems in large cities.     

Shock Wave Cleaning of Air Filters

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 SO₂ concentrations measured at urban sites in the eastern and midwestern U.S. are consistent with the corresponding reductions in local SO₂ emissions, but these decreases have been accompanied by only modest decreases in ambient sulfate concentrations. Large differences in the amounts of SO₂ 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 SO₂ 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 SO₂ emission levels and patterns of emissions clearly demonstrates the higher ambient sulfate concentration levels in eastern air quality control regions. Relationships between SO₂, 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 SO₂ 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.