A Comparison of the Size Distribution of Particulates Emitted from Air,Mechanical, and Steam Atomized Oil Fired Burners

Particulate size distributions were obtained in the effluent gases from three steam generating boilers of a power station employing mechanical, steam, and air systems for heavy fuel atomization. Samples were obtained with an eight-stage cascade impactor. The air atomized burner produced the lowest particulate loading, the greatest percentage of particulates by weight in the submicron range, and particulates with the lowest combustible content.     

Development of a variable configuration cascade impactor for aerosol size distribution measurement

In atmospheric aerosol studies, it is often required to use two different impactors, namely, the normal pressure and the low-pressure impactor, to measure the mass-size distribution over a wide size range. From the perspective of rendering the system compact for such measurements, it may be more advantageous to combine the two features in a single instrument. In an effort towards exploring this option, a variable configuration cascade impactor (VCCI) comprising of 7 normal pressure and 4 low-pressure stages has been designed and developed. In configuration-1, it operates as a low-pressure impactor, with a sampling flow rate of 10 L min^?1 and classifies the particles from 0.1 to 21 μm in eleven size classes. In configuration-2, it operates as a normal pressure impactor, with a sampling flow rate of 45 L min^?1, and classifies the particles from 0.53 to 10 μm in seven size classes. As part of performance evaluation of the system, the deposit patterns and the integral performance have been studied. For integral performance, a comparative mass-size distribution measurement between VCCI and standard Andersen impactor was carried out. Its performance was also evaluated against the GRIMM Scanning Mobility Particle Sizer (SMPS) in the common size range of both these instruments and against GRIMM Optical Particle Counter (OPC). In addition to this, VCCI was evaluated for its performance in the PM_x configuration obtained by removing a few of the impactor stages sequentially and measuring corresponding size distribution for every stage removed. Changes in the distribution parameters due to spillover of the deposits of previous stage to remaining stages were within 10%. This variation is well within the generally accepted value for all environmental measurement related applications.     

空气中多环芳烃的研究现状

本文比较系统地讨论了空气中多环芳烃（ＰＡＨｓ）的研究现状。重点介绍了空气颗粒物及气相中多环芳烃的采样分析新办法，城市大气及居民室内外空气中多环芳烃的污染状况及其来源，简单介绍了人体接触多环芳烃的水平，指标及空气中多环芳烃的健康风险评价的研究概况。共引文献１２９篇。     

High Volume Sampling: Errors Incurred during Passive Sample Exposure Periods

The current Federal EPA reference method for the determination of total suspended particulate matter (TSP) in the atmosphere is the high volume method (hi-vol).¹ The hi-vol sampler is normally operated for a 24 hr period by drawing air through an 8 X 10 in. glass fiber filter at an air sampling flow rate of between 40-60 cfm. TSP samples are presently collected in this manner every 6th day (61 samples/year). Results are used to determine compliance with existing National Primary Ambient Air Quality Standards for TSP (i.e., 260 µg/m³, maximum 24 hr average, not to be exceeded more than once a year; 75 µg/m³, annual geometric mean). However, when the sampling frequency is diminished to only 61 out of a possible 365 measurements each year, the degree of certainty associated with meeting these air quality standards is also decreased.^2,3 This partial sampling schedule also introduces other sampling errors. One such error caused by the exposure of the collection filter both prior and subsequent to the desired sampling day is the subject of the following discussion.     

A Field Intercomparison and Fundamental Characterization of Various Dust Samplers with a Reference Sampler

The European Economic Community Council Directive 80/779/EEC¹ describes air quality limit values and guide values for sulfur dioxide and suspended particulates. However, article 10, paragraph 1 does not define well enough the reference method required, amongst others, for the gravimetric measurement of suspended particulates. It is explicity stated in article 10, paragraph 5 of the directive, that “the commission shall, in selected locations in the member states and in cooperation with the latter, carry out studies on the sampling…of suspended particulates. These studies shall be designed in particular to promote the harmonization of methods of sampling and analysis of these pollutants.” Therefore, in a joint research program the Umweltbundesamt (grant #104 02263), the commission of European Communities (grant #84-B-6642-11-017-11-N) and the U.S. EPA (grant #2-43211-3580) funded the development of a reference dust sampler by the Fraunhofer-lnstitute of Toxicology and Aerosol Research (FhITA, in Hannover, Federal Republic of Germany) in order: ? to study the particle size distribution of ambient air aerosol at a number of selected sites;

? to compare the results obtained with the reference dust sampler with those of particle samplers operated in Europe and the United States;

? to verify the applicability of wind tunnel results to sampling behaviour in the free atmosphere.

     

Applicability of a modified MCE filter method with Button Inhalable Sampler for monitoring personal bioaerosol inhalation exposure

In this study, a “modified” mixed cellulose ester (MCE) filter culturing method (directly placing filter on agar plate for culturing without extraction) was investigated in enumerating airborne culturable bacterial and fungal aerosol concentration and diversity both in different environments. A Button Inhalable Sampler loaded with a MCE filter was operated at a flow rate of 5 L/min to collect indoor and outdoor air samples using different sampling times: 10, 20, and 30 min in three different time periods of the day. As a comparison, a BioStage impactor, regarded as the gold standard, was operated in parallel at a flow rate of 28.3 L/min for all tests. The air samples collected by the Button Inhalable Sampler were directly placed on agar plates for culturing, and those collected by the BioStage impactor were incubated directly at 26 °C. The colony forming units (CFUs) were manually counted and the culturable concentrations were calculated both for bacterial and fungal aerosols. The bacterial CFUs developed were further washed off and subjected to polymerase chain reaction–denaturing gradient gel electrophoresis (DGGE) for diversity analysis. For fungal CFUs, microscopy method was applied to studying the culturable fungal diversity obtained using different methods. Experimental results showed that the performance of two investigated methods varied with sampling environments and microbial types (culturable bacterial and fungal aerosols). For bacterial aerosol sampling, both methods were shown to perform equally well, and in contrast the “modified” MCE filter method was demonstrated to enumerate more culturable fungal aerosols than the BioStage impactor. In general, the microbial species richness (number of gel bands) was observed to increase with increasing collection time. For both methods, the DGGE gel patterns were observed to vary with sampling time and environment despite of similar number of gel bands. In addition, an increase in sampling time from 20 to 30 min was found not to substantially alter the species richness. Regardless of the sampling methods, more species richness was observed in the outdoor environment than the indoor environment. This study described a new personal bioaerosol exposure assessment protocol, and it was demonstrated applicable in monitoring the personal bioaerosol exposure in replace of an Andersen-type impactor.     

Severe particulate pollution from the deposition practices of the primary materials of a cement plant

Global cement production has increased twofold during the last decade. This increase has been accompanied by the installation of many new plants, especially in Southeast Asia. Although various aspects of pollution related to cement production have been reported, the impact of primary material deposition practices on ambient air quality has not yet been studied. In this study, we show that deposition practices can have a very serious impact on levels of ambient aerosols, far larger than other cement production-related impacts. Analyses of ambient particulates sampled near a cement plant show 1.3–30.4 mg/m³ total suspended particulates in the air and concentrations of particles with a diameter of 10 μm or less at 0.04–3 mg/m³. These concentrations are very high and seriously exceed air quality standards. We unequivocally attribute these levels to outdoor deposition of cement primary materials, especially clinker, using scanning electron microscopy/energy-dispersive X-ray spectroscopy. We also used satellite-derived aerosol optical depth maps over the area of study to estimate the extent of the spatial impact. The satellite data indicate a 33 % decrease in aerosol optical depth during a 10-year period, possibly due to changing primary material deposition practices. Although the in situ sampling was performed in one location, primary materials used in cement production are common in all parts of the world and have not changed significantly over the last decades. Hence, the results reported here demonstrate the dominant impact of deposition practices on aerosol levels near cement plants.     

Metallic Element Composition of Particulate Matter During Day and Night Sampling at a Traffic Site

Day and night period sampling programs were carried out using a versatile air pollutant system to collect fine particulate matter (PM_2.5) and coarse particulate matter (PM_2.5–10) simultaneously at a traffic junction that is only 60 m from HungKuang University located in Central Taiwan. Therefore, HungKuang University is regarded as the traffic sampling site in this study. Similar measurements were carried out in a previous 2013 study by Fang and colleagues during October 2012 to November 2012. Determination of metallic element composition of fine and coarse particulates collected during the day and the night was accomplished with inductively coupled plasma atomic emission spectrometry (ICP-AES). The results indicated that there were no significant differences in composition of metallic elements Zn, Cu, Cr, Mn, Fe, Pb, and Cd in either coarse or fine particles for both day and night sampling periods. The statistical results indicated no significant differences for metallic elements in the PM_2.5–10 particulates for day and night sampling periods. Also, no significant differences were noted for metallic elements in the PM_2.5 particulates for day and night sampling periods at this traffic sampling site. The proposed reason is the limited sampling period employed in this study. Another potential reason is the presence of traffic that runs heavily both day and night being a major contributor to the ambient air metallic pollutants in this region.     

Quality control for sampling of PCDD/PCDF emissions from open combustion sources

Both long duration (>6 h) and high temperature (up to 139 °C) sampling efforts were conducted using ambient air sampling methods to determine if either high volume throughput or higher than ambient air sampling temperatures resulted in loss of target polychlorinated dibenzodioxins/dibenzofurans (PCDDs/PCDFs) from a polyurethane foam (PUF) sorbent. Emissions from open burning of simulated military forward operating base waste were sampled using EPA Method TO-9A for 185 min duration using a filter/PUF/PUF in series combination. After a 54 m³ sample was collected, the sampler was removed from the combustion source and the second PUF was replaced with a fresh, clean PUF. An additional 6 h of ambient air sampling (171 m³) was conducted and the second PUF was analyzed to determine if the PCDD/PCDF transferred from the filter and the first PUF. Less than 4.4% of the initial PCDD/PCDF was lost to the second PUF. To assess the potential for blow off of PCDD/PCDF analytes during open air sampling, the mobility of spiked mono- to hepta-PCDD/PCDF standards across a PUF sorbent was evaluated from ambient air temperatures to 145 °C with total volumes between 600 L and 2400 L. Lower molecular weight compounds and higher flow amounts increased release of the spiked standards consistent with vapor pressure values. At 600 L total sampled volume, the release temperature for 1% of the tetra-CDD (the lowest chlorinated homologue with a toxic compound) was 87 °C; increasing the volume fourfold reduced this temperature to 73 °C.     

Development and Evaluation of an Impactor for a PM2.5 Speciation Sampler

ABSTRACT

A conventional impactor for a particle speciation sampler was developed and validated through laboratory and field tests. The speciation sampler consists of the following components: a PM_2.5 conventional impactor that removes particles larger than 2.5 μm, an all-glass, coated honeycomb diffusion denuder, and a 47-mm filter pack. The speciation sampler can operate at two different sampling rates: 10 and 16.7 L/min. An experimental characterization of the impactor’s performance was conducted. The impactor’s collection efficiency was examined as a function of critical design parameters such as Reynolds number, the distance from the nozzle exit to the impac-tion plate, and the impaction substrate coating method. The bounce of particles larger than the cut point was successfully minimized by using a greased surface as the im-paction substrate. Additionally, a series of field intercomparison experiments were conducted at both 10 and 16.7 L/min airflow. PM_2.5 mass and SO₄ ^2- concentrations were measured and compared with the Federal Reference Method (FRM) and found to be in good agreement. Results of the laboratory chamber tests also indicated that the impactor’s performance was in good agreement with the FRM.     

Concentrations of particulate matter emitted from large cattle feedlots in Kansas

Particulate matter (PM) emitted from cattle feedlots are thought to affect air quality in rural communities, yet little is known about factors controlling their emissions. The concentrations of PM (i.e., PM2.5, PM10, and total suspended particulates or TSP) upwind and downwind at two large cattle feedlots (KS1, KS2) in Kansas were measured with gravimetric samplers from May 2006 to October 2009 (at KS1) and from September 2007 to April 2008 (at KS2). The mean downwind and net (i.e., downwind - upwind) mass concentrations of PM2.5, PM10, and TSP varied seasonally, indicating the need for multiple-day, seasonal sampling. The downwind and net concentrations were closely related to the moisture content of the pen surface. The PM2.5/PM10 and PM2.5/TSP ratios at the downwind sampling location were also related to the moisture content of the pen surface, humidity, and temperature. Measurement of the particle size distribution downwind of the feedlot with a cascade impactor showed geometric mean diameter ranging from 7 to 18 microm, indicating that particles that were emitted from the feedlots were generally large in size.     

Flexibility of X-Ray Emission Spectrography as Adapted to Microanalysis of Air Pollutants

Methods previously published by this laboratory for analyzing thin dust coatings of airborne particulates have been further evaluated, as applied to vast air pollution surveys. It was demonstrated that choice of glass fiber filters adapted to high-volume samplers restricts the analysis to a limited number of elements, such as lead. More flexibility and versatility are attained through the use of organic membrane filters mounted in small plastic monitors which permit multi-elemental analysis at least as accurately as with other popular but time-consuming techniques. These qualities of speed and accuracy allow shorter intervals of sampling which are normally required for better statistical assessment of broad air pollution surveys. Sensitivity of the technique reaches a value close to 0.05 μg/m³, while time of analysis required is about five minutes per element after receipt of the sample.     

新型多级冲击采样器切割粒径的标准粒子实验分析

大气溶胶对环境污染、气候变化以及人体健康有着重要的影响,大气溶胶的采集和分析已成为当前大气环境研究领域中的一个重要课题.论述的新型多级冲击采样器能够实现大气溶胶颗粒物按空气动力学粒径的大小7级分离采集,提供大致均匀的平面样品以进行后续的物理、化学分析,同时保证各分级切割粒径的稳定性.利用振动孔溶胶发生器产生均匀、粒径大致相同、单分散相的1.5～17μm空气动力学粒径标准粒子,对新型多级冲击采样器前三级的切割粒径和收集效率进行鉴定性分析实验,结果表明,能够满足对大气溶胶颗粒物分级采集的要求.     

Environmental Issues—Persistent Problems and Emerging Challenges

Abstract

A field study was performed to evaluate indoor air concentrations and vapor intrusion (VI) of tetrachloroethylene (PCE) and other chlorinated solvents at a commercial retail site in Dallas, TX. The building is approximately 40 yr old and once housed a dry cleaning operation. Results from an initial site characterization were used to select sampling locations for the VI study. The general approach for evaluating VI was to collect time-integrated canister samples for off-site U.S. Environmental Protection Agency Method TO-15 analyses. PCE and other chlorinated solvents were measured in shallow soil gas, subslab soil-gas, indoor air, and ambient air. The subslab soil gas exhibited relatively high values: PCE ≤2,600,000 parts per billion by volume (ppbv) and trichloroethylene ≤170 ppbv. The attenuation factor, the ratio of indoor air and subslab soil-gas concentrations, was unusually low: approximately 5 x 10^-6 based on the maximum subslab soil-gas concentration of PCE and 1.4 x 10^-5 based on average values.     

Indoor-outdoor relationship of suspended particulate matter and its chemical composition at different sizes

The indoor-outdoor concentration relationship of particulate matter PM_9.0 (aerodynamic diameter 9 μm or smaller) and its chemical composition (sulfate, nitrate, chloride and ammonium) has been studied. Samples were collected using four identical Anderson impactors, each one collecting nine size ranges by eight impactor stages (9, 5.8, 4.7, 3.3, 2.1, 1.1, 0.65 and 0.43 μm) plus a back-up filter representing particles finer than 0.45 μm. Concentrations of sulfate, nitrate and chloride were determined by ion chromatography, and an ammonium-selective ion electrode plus a Corning pH ion meter were used to determine ammonium ion. The results revealed that sulfate was the predominant component and chloride the least abundant. The size distribution of sulfate, nitrate and ammonium very strongly peaked near 0.65 μm and with very little at the larger sizes. The chloride concentration was depleted in the fine particles and enhanced in the relatively coarser particles, with the peak at 3.3 μm. All these concentrations had a significant linear relationship with mass concentrations in outdoor samples. In indoor samples, the same relation was observed only for sulfate and ammonium, which were also significantly correlated with each other. Furthermore, indoor sulfate, chloride and ammonium concentrations were higher towards the finest particle sizes, indicating a higher potential inhalation health hazard. The study also confirmed that indoor air quality depends on outdoor atmospheric pollution level, indoor activities and virtually on the particle size. Finally, the study would assist in selecting the type of collector required to reduce the level of particulates to an acceptable level for indoor ambient air.     

A field intercomparison and fundamental characterization of various dust samplers with a reference sampler

The European Economic Community Council Directive 80/779/EEC describes air quality limit values and guide values for sulfur dioxide and suspended particulates. However, article 10, paragraph 1 does not define well enough the reference method required, amongst others, for the gravimetric measurement of suspended particulates. It is explicity stated in article 10, paragraph 5 of the directive, that "the commission shall, in selected locations in the member states and in cooperation with the latter, carry out studies on the sampling...of suspended particulates. These studies shall be designed in particular to promote the harmonization of methods of sampling and analysis of these pollutants." Therefore, in a joint research program the Umweltbundesamt (grant #104 02263), the commission of European Communities (grant #84-B-6642-11-017-11-N) and the U.S. EPA (grant #2-432U-3580) funded the development of a reference dust sampler by the Fraunhofer-Institute of Toxicology and Aerosol Research (FhlTA, in Hannover, Federal Republic of Germany) in order: to study the particle size distribution of ambient air aerosol at a number of selected sites; to compare the results obtained with the reference dust sampler with those of particle samplers operated in Europe and the United States; to verify the applicability of wind tunnel results to sampling behaviour in the free atmosphere.     

Monitoring personal,indoor, and outdoor exposures to metals in airborne particulate matter: Risk of contamination during sampling,handling and analysis

Rigorous sampling and quality assurance protocols are required for the reliable measurement of personal, indoor and outdoor exposures to metals in fine particulate matter (PM_2.5). Testing of five co-located replicate air samplers assisted in identifying and quantifying sources of contamination of filters in the laboratory and in the field. A field pilot study was conducted in Windsor, Ont., Canada to ascertain the actual range of metal content that may be obtained on filter samples using low-flow (4 L min⁻¹) 24-h monitoring of personal, indoor and outdoor air. Laboratory filter blanks and NIST certified reference materials were used to assess contamination, instrument performance, accuracy and precision of the metals determination. The results show that there is a high risk of introducing metal contamination during all stages of sampling, handling and analysis, and that sources and magnitude of contamination vary widely from element to element. Due to the very small particle masses collected on low-flow 24-h filter samples (median 0.107 mg for a sample volume of approximately 6 m³) the contribution of metals from contamination commonly exceeds the content of the airborne particles being sampled. Thus, the use of field blanks to ascertain the magnitude and variability of contamination is critical to determine whether or not a given element should be reported. The results of this study were incorporated into standard operating procedures for a large multiyear personal, indoor and outdoor air monitoring campaign in Windsor.     

Effect of typhoon on atmospheric particulates in autumn in central Taiwan

Previous studies have suggested that the ongoing global climate change will likely increase the intensity and frequency of extreme weather, such as typhoons. Since the beginning of global warming, it has become necessary to understand the influence of typhoons on air quality. Rare data, especially particulate measurements data could be used to establish the relationship between the air pollution and typhoons. One of main limiting factors is that most of the previous chemical analyses of particulates used a relatively long sampling time, which could dilute the temporal impact of particulate characteristics and their sources. This work, depending more time-resolved measurements, focus on the characteristics and sources of high particulate matter levels and the influence of typhoons and the Pacific high system. Depending on the measurements, two pollutant groups were clearly identified in this work. The first pollutant group was the emissions from neighboring riverbeds under the strong circulation of the typhoon in the driest season and characterized as high coarse particle concentrations with high mass fraction of Ca²⁺. The second pollutant group was characterized as the formation and transport of secondary particles with prevalent ions of NH₄⁺, NO₃^?, and SO₄^2? and occurred in the sea-land breeze circulation under the influence the Pacific high system.     

A Technique for Respirable Sampling

The purpose of this paper is to describe instrumentation to aerodynamically size suspended particulates found in ambient air and to summarize results of field testing utilizing the new technique.

A four-stage, multiorifice high-volume fractionating impactor with backup filter, which can be operated as a component of the standard high-volume sampler, collects particulate matter in five separate aerodynamic size ranges: 7 micrometer (μm) or larger, 3.3 to 7 μm, 2.0 to 3.3 μm, 1.1 to 2.0 μm, and 0.01 to 1.1 μm.

Comparative field tests utilizing duplicate sampling techniques were conducted to determine the feasibility of using the size fractionator on a routine basis in field operations. Verification of the actual particle size separation was not undertaken; however, earlier tests utilizing laboratory-generated aerosols have been performed with satisfactory results.

The results of field tests indicate that the fractionator can be used to determine the aerodynamic size distribution of particulate matter. A glass fiber surface with a pH of 11.0 was found to adsorb atmospheric acid gases during sampling and thus gave erroneous mass concentration results when compared to the standard high-volume sampler. Glass fiber filters with a pH of 6.5 eliminated the acid gas adsorption.     

Size resolved chemical mass balance of aerosol particles over rural Hungary

The mass size distribution of atmospheric aerosol particles was determined by means of an electric low pressure impactor (ELPI) in rural air in Hungary. The particles captured on different stages of the impactor were chemically analyzed by capillary zone electrophoresis to quantify ionic components as well as by catalytic combustion method to detect total carbon in the samples. The results show that fine aerosol consists mainly of ammonium sulfate and organic carbon. These two species have rather different size distributions since very small particles are composed almost of carbon compounds. The analysis of fine aerosol samples collected simultaneously on filters indicates that an important part of organics is soluble in water. The mass balance of fine particles as a function of their size is estimated by taking into account the liquid water adsorbed by ammonium sulfate and by converting the mass of carbon to the mass of carbon compounds. Finally, the size resolved mass balance of fine aerosol particles is presented and discussed as a function of the origin of air masses.