Atmospheric Aerosols: Size Distribution Interpretation

The body of information presented in this paper is directed towards the scientist or engineer who measures and interprets the physical characteristics of ambient air. This paper interprets measurements made with the Minnesota Aerosol Analyzing System (MAAS) in Denver, near Denver, and near Ft. Collins, Colo., and examines the measurements in the light of what has been learned from several thousand size distributions measured in the other parts of the United States. The origin and physical change of atmospheric particulates is examined through interpretation of modes occurring in the size distributions. The mode coined “AHken Nuclei Range” mode is a measure of aerosol generation, while aged aerosols show up in the “Accumulation Range” mode. Windblown dusts, sea sprays, and mechanically produced particles such as fly ash generate a “Coarse Particle Range” mode. The air environment is categorized into several types of background and urban aerosols whose physical characteristics are described by a limited number of parameters. These categories are exemplified and discussed.     

Calculated Droplet Size Distributions and Opacities of Condensed Sulfuric Acid Aerosols

The properties of condensed polydisperse sulfuric acid aerosols in industrial flue gas were calculated. The condensed aqueous acid volume concentration, composition, droplet size distributions and condensed plume opacity were calculated for typical flue gas compositions, condensation nucleus size distributions and flue gas dilution ratios. The assumed initial flue gas at 170°C contained 0.035 g/acm fly ash particles, 1-20% water vapor, and 1-50 ppmv sulfuric acid vapor. The assumed gas cooling mechanism was by adiabatlc dilution with cool ambient air. Polydisperse droplet growth was calculated by assuming equal surface area increase for each particle. The calculations show that sulfuric acid condensation should have minimal effect on particles larger than 1 μm, but will form a high concentration of particles in the narrow size range of 0.05-0.5 μm diameter. Depending on the initial sulfuric acid and water vapor concentrations in the hot flue gas, the calculated maximum plume opacity following gas dilution ranged from 5% to 25%, compared to 4% for the dry condensation nucleus aerosol.     

Aerosols in a Mediterranean Forest: Sulfates,Particle Size Distribution,and Growth Rates

ABSTRACT

Particle size distribution measurements in 16 nonlinear intervals covering the 0.1–7.5 μm range and concurrent sulfate concentrations were continuously recorded in September 1996 over the period of two weeks in a Mediterranean forest. Sulfate size distribution was derived from a linear correlation fit between the concentrations and the number of particles recorded at each particle size interval. The results revealed two modal diameters for sulfates, with typical diameters at 0.3 and 0.675 μm. These results were associated with two different dominant chemical mechanisms governing sulfate formation.

In order to describe the dominant chemical mechanism, the growth law approach was applied. Growth rates were determined using the parameter estimates of the fitted particle size distribution function. By matching these data with sulfate concentrations, the dominant chemical reactions were identified. The results have shown that sulfate formation is governed by both homogeneous and heterogeneous reactions and that the latter process was dominant. Condensation reactions prevailed in the early morning and late afternoon, and volume reactions at night, particularly in high-moisture conditions. From the observational data, the gas-to-particle conversion rate for sulfur dioxide (SO₂) at nighttime was also derived, yielding a 2.18%/hr^-1.     

Modeling Inorganic Aerosols and Their Response to Changes in Precursor Concentration in Mexico City

Abstract

Based on data from the 1997 Investigación sobre Materia Particulada y Deterioro Atmosférico-Aerosol and Visibility Evaluation Research (IMADA-EVER) campaign and the inorganic aerosol model ISORROPIA, the response of inorganic aerosols to changes in precursor concentrations was calculated. The aerosol behavior is dominated by the abundance of ammonia and thus, changes in ammonia concentration are expected to have a small effect on particle concentrations. Changes in sulfate and nitrate are expected to lead to proportional reductions in inorganic fine particulate matter (PM_2.5). Comparing the predictions of ISORROPIA with the observations, the lowest bias and error are achieved when the aerosols are assumed to be in the efflorescence branch. Including crustal species reduces the bias and error for nitrate but does not improve overall model performance. The estimated response of inorganic PM_2.5 to changes in precursor concentrations is affected by the inclusion of crustal species in some cases, although average responses are comparable with and without crustal species. Observed concentrations of particle chloride suggest that gas phase concentrations of hydrogen chloride may not be negligible, and future measurement campaigns should include observations to test this hypothesis. Our ability to model aerosol behavior in Mexico City and, thus, design control strategies, is constrained primarily by a lack of observations of gas phase precursors. Future campaigns should focus in particular on better understanding the temporal and spatial distribution of ammonia concentrations. In addition, gas phase observations of nitric acid are needed, and a measure of particle water content will allow stable versus metastable aerosol behavior to be distinguished.     

Composition,Size and Control of Automotive Exhaust Particulates

This paper on automobile exhaust particulates describes total particulate composition, size of exhausted lead particulates, and the effects of traps on total lead emitted. This study was conducted using cars manufactured during 1966-1970. Work in suspended particulate emission from several vehicles operated on a chassis dynamometer under Federal 7-mode cycle conditions has shown: (1 ) cars vary widely in the amounts and composition of their particulate emissions; (2) cold-cycle operation gives 2-8 times more particulate than hot engine operation; (3) lead compounds represent less than one-third of total particulates, the remainder being carbon compounds along with ammonium and nitrate ions and unknown materials; (4) carbon emission for stabilized cars using leaded gasoline varies widely but averages about 35% of the total; (5) suspended particulate emissions are nearly equal with new cars whether or not lead is present; (6) exhausted lead varies with the condition of the exhaust system and ranges between 7 and 30% of the lead consumed by the engine; (7) fuel additives affect the amount of emitted particulates; (8) probe sampling techniques underestimate by a large factor the amount of particulates emitted by vehicles; and (9) trapping systems offer potential for greatly reducing the emission of suspended total particulates.     

Environmental Impact of Residential Wood Combustion Emissions and its Implications

Currently available information suggests a substantial environmental impact from residential wood combustion emissions. Air pollution from this source is widespread and increasing. Current ambient measurements, surveys, and model predictions indicate winter respirable (<2 μm) emissions from residential wood combustion can easily exceed all other sources. Both the chemical potency and deliverability of the emissions from this source are of concern. The emissions are almost entirely in the inhalable size range and contain toxic and priority pollutants, carcinogens, co-carcinogens, cilia toxic, mucus coagulating agents, and other respiratory irritants such as phenols, aldehydes, etc. This source is contributing substantially to the nonattainment of current particulate, carbon monoxide, and hydrocarbon ambient air quality standards and will almost certainly have a significant impact on potential future standards such as inhalable particulates, visibility, and other chemically specific standards. Emission from this growing source is likely to require additional expenditures by industry for air pollution control equipment in nonattainment areas.     

Overview of Traditional and Environmental Factors Related to Bone Health

Environmental Science and Pollution Research - Bone mass in adulthood depends on growth and mineralization acquired during childhood and adolescence. It is well known that these stages of life are...     

One-Year Study of the Elemental Composition and Source Apportionment of PM10 Aerosols in Florence,Italy

Abstract

An extensive investigation was carried out for the characterisation of the air particulate composition in Florence. The aim was to determine the aerosol elemental concentrations, as well as to identify pollution sources. For our investigation, the external Particle-Induced X-Ray Emission–Particle-Induced γ-Ray Emission beam facility of the Istituto Nazionale di Fisica Nucleare, Van de Graaff accelerator at the Physics Department of the Florence University was used. We report the results of the analysis of a long temporal series (approximately 1 yr) of PM₁₀ particulate samples, collected on Millipore filters on a daily basis in three different sites (characterised by different urban settings). Daily concentrations of more than 20 elements were detected. The long sampling period (approximately 1 yr) allowed a comparison with the air quality recommended values and the identification of seasonal variations. Four main sources (traffic, oil-combustion, soil-dust, and wind transported sea-salt) were extracted with the help of Principal Component Analysis (PCA). An absolute PCA showed traffic to be the major source both in the high traffic site and in the urban background site.     

Establishing Relevant Ozone Standards to Protect Vegetation and Human Health: Exposure/Dose-Response Considerations

For assessing the efficacy of a specific form of the National Ambient Air Quality Standard for 0₃, those exposure patterns that result in vegetation and human health effects must be identified. For vegetation, it has been found that the higher hourly average concentrations should be weighted more than the lower concentrations. Controlled human exposure work supports the suggestion that concentration may be more important than exposure duration and ventilation rates. It has been indicated in the literature that the current form of the federal 0₃ standard may not be appropriate for protecting vegetation and human health from 0₃ exposures. The proposed use of the cumulative index alone as a form of the standard may not provide sufficient protection to vegetation. An extended-period average index, such as a daily maximum 8-hour average concentration, may not be appropriate to protect human health because of the reduced ability to observe differences among hourly 0₃ concentrations exhibited within exposure regimes. For both vegetation and human health effects research, additional experimentation is required to identify differences in responses that occur when ambient-type exposure regimes are applied. Any standard promulgated to protect vegetation and human health from 0₃ exposures should consider combining cumulative exposure indices with other parameters so that those unique exposures that have the potential for eliciting an adverse effect can be adequately described.     

The Transfer of Trichloroethyene (TCE) from a Shower to Indoor Air: Experimental Measurements and Their Implications

Experiments were performed to measure the transfer of trlchloroethylene (TCE), a volatile organic compound (VOC), from tap water In showers to Indoor air. In these experiments, the loss of TCE from tap water in the shower is based on the difference between Influent and effluent concentrations. We have developed and previously published a three-compartment model, which we use to simulate the 24-h concentration history of VOCs in the shower, bathroom, and remaining household volumes resulting from the use of contaminated tap water. An important input to this model is the transfer efficiency of the VOC from water to air. The experiments reveal that the transfer efficiency of TCE from shower water to air has an arithmetic mean value of 61 percent and an arithmetic standard deviation of 9 percent. Analysis of the results shows that there Is no statistically significant difference between the transfer efficiency measured with hot (37°C) or cold (22°C) shower water and that there Is no statistically significant change In transfer efficiency with time during a 20-mln shower. The implications for exposure assessment are considered.     

The Steubenville Comprehensive Air Monitoring Program (SCAMP): Concentrations and Solubilities of PM2.5 Trace Elements and Their Implications for Source Apportionment and Health Research

Abstract

The elemental compositions of the water-soluble and acid-digestible fractions of 24-hr integrated fine particulate matter (PM_2.5) samples collected in Steubenville, OH, from 2000 to 2002 were determined using dynamic reaction cell inductively coupled plasma-mass spectrometry. The water-soluble elemental compositions of PM_2.5 samples collected at four satellite monitoring sites in the surrounding region were also determined. Fe was the most abundant but least water soluble of the elements determined at the Steubenville site, having a mean ambient concentration of 272 µg/m³ and a median fractional solubility of 6%. Fe solubility and its correlations with SO₄ ^2? and temperature varied significantly by season, consistent with the hypothesis that secondary sulfates may help to mobilize soluble Fe under suitable summertime photochemical conditions. Significantly higher ambient concentrations were observed at Steubenville than at each of the four satellite sites for 10 of the 18 elements (Al, As, Ca, Cd, Fe, Mg, Mn, Na, Pb, and Zn) determined in the water-soluble PM_2.5 fraction. Concentrations of Fe, Mn, and Zn at Steubenville were substantially higher than concentrations reported recently for larger U.S. cities. Receptor modeling identified seven sources affecting the Steubenville site. An (NH₄)₂SO₄-dominated source, likely representing secondary PM_2.5 from coal-fired plants to the west and southwest of Steubenville, accounted for 42% of the PM_2.5 mass, and two sources likely dominated by emissions from motor vehicles and from iron and steel facilities in the immediate Steubenville vicinity accounted for 20% and 10%, respectively. Other sources included an NH₄NO₃ source (15%), a crustal source (6%), a mixed nonferrous metals and industrial source (3%), and a primary coal combustion source (3%). Results suggest the importance of very different regional and local source mechanisms in contributing to PM_2.5 mass at Steubenville and reinforce the need for further research to elucidate whether metals such as Fe, Mn, and Zn play a role in the PM_2.5 health effects observed previously there.     

Comparing the Community Composition of European and Eastern Chinese Waterbirds and the Influence of Human Factors on the China Waterbird Community

We compared the European and eastern Chinese waterbird assemblages and checked whether the effects of human disturbance could be detected in the assemblages’ composition. For the different Chinese provinces, we expected to find a negative effect of economic development on the mean bird species mass and on the proportion of bentivorous, piscivorous and insectivorous bird species. We also expected to find relatively fewer large species in the Chinese assemblage. Species rank–abundance curves were relatively similar, but China had significantly more species with smaller body masses. The China assemblage was characterized by relatively higher abundance of heavy-bodied species, contrary to our expectations. Mean bird body mass decreased in China with increasing disturbance and increasing gross domestic product (GDP). For coastal provinces in China the percentage of bentivorous, piscivorous and insectivorous bird species declined with increasing GDP, maybe through the increased use of pesticides or fertilizer.     

Particle Size Distributions and Elemental Composition of Atmospheric Particulate Matter in Southern Italy

Abstract

Three 2-wk seasonal field campaigns were performed in 2003 and 2004 at a sampling site on the southern Tyrrhenian coast of Italy with the aim to investigate the dynamics and characteristics of particle-bound pollutants in the Mediterranean area. Fine (PM_2.5) and coarse particulate matter (PM_10–2.5) size fractions were collected by a manual dichotomous sampler on 37-mm Teflon filters over a 24-hr sampling period. On average, 70% of the total PM₁₀ (PM_2.5 + PM_10–2.5) mass was associated with the coarse fraction and 30% with the fine fraction during the three campaigns. The ambient concentrations of Pb, Ni, Cr, Zn, Mn, V, Cd, Fe, Cu, Ca, and Mg associated with both size fractions were determined by atomic absorption spec-trometry. Ambient concentrations showed differences in their absolute value, ranging from few ng · m^-3 to µg ?m^-3, as well as in their variability within the PM_2.5 and PM_10–2.5 size fractions. PM₁₀ levels were well below the European Union (EU) limit value during the study period with the exception of three events during the first campaign (fall) and five events during the third campaign (spring). Two main sources were identified as the major contributors including mineral dust, transported from North Africa, and sea spray from the Tyrrhenian Sea. Comparing the results with backward trajectories, calculated using the Hybrid Single-Particle Lagrangian Integrated Trajectory Model (HYSPLIT) and Total Ozone Mapping Spectrometer-National Aeronautics and Space Administration (TOMS-NASA) maps, it was observed that in central and eastern Europe, the Tyrrhenian Sea and North Africa were the major emission source regions that affected the temporal variations and daily averages of PM_2.5 and PM_10–2.5 concentrations.     

影响恶臭监测结果的因素及其对策

使用三点比较式臭袋法进行恶臭监测，对经常影响监测结果的几个因素加以分析，并提出相应的对策。     

Atmospheric Aerosol Composition and Concentration as a Function of Particle Size and of Time

As a step toward better understanding the reactive Los Angeles air basin atmosphere, a study was undertaken at the University of California—Riverside Campus, to determine the composition and concentration of atmospheric particulate matter as a function of particle size and time. The study involved developing a method for obtaining size-classified, time-fractionated aerosol samples amenable to chemical and physical (including microscopic) analysis. During a 15-day period, samples were obtained over 4-hr periods and subsequently analyzed for nitrate, sulfate, iron, and lead. Concentration of six gaseous pollutantsj total aerosol light-scattering, and several meteorological measurements were simultaneously recorded and averaged over the 4-hr intervals. This data was presented graphically to show the diurnal variation in and relationship between gaseous, particulate, and meteorological measurements. A strong relationship between gaseous peroxyacetyl nitrate, particulate nitrate, and aerosol light-scattering was found. High concentrations of ammonium nitrate particles, mainly in the 0.5-2μ, diameter size range, were found in the atmospheric particulate samples collected on days of very high smog (very limited visibility).     

Combustion sources of particles. 1. Health relevance and source signatures

Combustion processes result in generation of a large number of particle and gaseous products that create health and environmental risks. Of particular importance are the very small particles that are emitted in large quantities from all the combustion sources, and that have been shown to be potentially more significant in terms of their impact on health than larger particles. To control and mitigate the particles with a view of health and environmental risk reduction, a good understanding is necessary of the relative and absolute contribution from the emission sources to the airborne concentrations. This understanding could only be achieved by developing source signature libraries through direct emission measurements from the sources on one hand, and by measuring particle concentrations in the air, and apportioning them to the specific local and distant sources using the signatures, on the other hand. This paper is a review of particle characteristics that are used as source signatures as well as their general advantages and limitations. The second part of the paper reviews source signatures of the most common combustion pollution sources.     

Concentration and Composition of Atmospheric Aerosols from the 1995 SEAVS Experiment and a Review of the Closure between Chemical and Gravimetric Measurements

ABSTRACT

We summarize the results from the various measurements and the inter-sampler comparisons from Southeastern Aerosol and Visibility Study (SEAVS), a study with one of its objectives to test for closure among chemical, gravimetric and optical measurements of atmospheric aerosol particles. Sulfate and organics are the dominant components of the SEAVS fine particles (nominally, particles with aerodynamic diameter <2.5 u,m) but between 28 and 42% (range over various samplers) of the gravimetrically measured total fine particle concentration is unidentified by the chemical measurements. Estimates of water associated with inorganic components and measurement imprecision do not totally explain the observed difference between gravimetric and chemical measurements. We examine the theoretical and empirical basis for assumptions commonly made in the published literature to extrapolate total fine particle concentration on the basis of chemical measurements of ions, carbon and elements.