The Coefficient of Haze as a Measure of Particulate Elemental Carbon

The technique to measure the coefficient of haze (COH) was developed in 1953 and was widely employed as a surrogate technique to measure total suspended particulate matter (TSP) in the 1960s. Because of the physical design of the sampler (known as the AISI Tape Sampler) used to measure COH, it was postulated that COH was directly related to the mass of fine elemental carbon particles (EC) with diameters less than 2.5 μm. To test the hypothesis, simultaneous samples of COH and EC were collected and analyzed during the 1981 Summer Study in Detroit. Regression analysis indicates that the two quantities are linearly related over the concentration range observed. Additional analyses indicate that COH is not related to TSP, fine particle mass, or light-scattering aerosol. Calculation of specific light absorption coefficients for EC from the COH data support the hypothesis that the tape sampler responds only to fine EC. A brief examination of historical COH data from Detroit suggests that the EC concentration has declined since 1972. This should be regarded as a preliminary assessment, however, until further verification of the COH-EC connection can be made.     

An Atmospheric Particulate Sampling Procedure For Gravimetric And Elemental Analyses

Large quantities of atmospheric aerosols with compositions SO₄ ⁼, NO₃ ^? and NH₄ ⁺ have been detected in highly industrialized areas. The major portions of aerosol products are the results of energyrelated fuel combustion. Both microphysical and macrophysical processes are considered in investigating the time dependent evolution of the saturation spectra of condensation nuclei associated with both polluted and clean atmospheres during the time periods of advection fog formation. The results show that the condensation nuclei associated with a polluted atmosphere provide more favorable conditions than condensation nuclei associated with a clean atmosphere to produce dense advection fog, and that attaining a certain degree of supersaturation is not necessarily required for the formation of advection fog with condensation nuclei associated with a polluted atmosphere for monodisperse distribution.     

Ambient Carbon Monoxide And Its Fate in the Atmosphere

Carbon monoxide, the most abundant air pollutant found in the atmosphere generally exceeds that of all other pollutants combined (excluding C0₂). An estimated tonnage of >87 X 10⁶ of CO was emitted in the United States from major technological sources alone during 1966. More than 90% of the total CO emitted from fossil fuels is derived from gasoline powered motor vehicles. Other sources of CO include emissions from coal and fuel oil burning, aircraft and open burning. Some CO is also formed by certain vegetation and marine invertebrates (siphonophores). Chemical reactions of CO in the upper and lower atmosphere are discussed. Chemical oxidation of CO in the lower atmosphere by molecular oxygen is very slow. The exact duration of CO in the lower atmosphere is not known with certainty; however, the mean residence time has been variously estimated to be between 0.3 and 5.0 years. In the absence of scavenging processes the estimated world-wide CO emission would be sufficient to raise the’atmospheric level by 0.03 ppm per year, yet the background levels of CO in clean air do not appear to be increasing. Several potential sinks are discussed. Knowledge of the mechanism of process of removal of CO from the lower atmosphere is unsatisfactory; the process, at the present time, cannot be identified with certainty.     

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.     

PM2.5中元素碳测定的研究进展

针对大气颗粒物中碳质细颗粒的不断深入研究，以及由此引发的环境污染问题，引用大量文献，从元素碳特性以及形成机理论述了各种元素碳测定技术及其特点，并结合国外的元素碳测定技术，探讨了国内相关技术的发展方向。     

Elemental Carbon Concentration in the Air Around Tampa Bay,Florida, 1990-1991

Elemental carbon (EC) particles have been found in the lungs of dolphins. The question arose as to whether these particles originated over land or water. This project determined the amount of EC particulate found in terrestrial air. Portions of paniculate filters and associated data collected during the period from January 1990 through December 1991 were provided by the Florida Department of Environmental Regulation. Using reflectance spectroscopy and laboratory-generated standards, atmospheric concentrations of EC and TSP were determined. This paper addresses the data from those counties which surround Tampa Bay.

In the spring of 1992, a television news station reported that researchers at Mote Marine Institute had found black carbon particulates in the lungs of dolphins (reported as “...dolphins with Black Lung Disease..."). The dolphins were found in the Gulf of Mexico off the coast of Florida.1 In discussions with a principal investigator of the dolphin study, the question arose as to whether these particulates came from urban or marine sources. No comprehensive investigation of soot concentrations in the air over Florida had been made. This study reports the elemental carbon (EC) content of urban particulate matter in the Tampa Bay region, where the affected dolphins were discovered between 1988 and 1990 (Sarasota County). This is the first step toward answering whether urban concentrations of EC were sufficient to contribute measurably to the EC found in the marine environment. Future efforts will address marine concentrations and sources of EC.

Elemental carbon, commonly termed “soot,” is a product of incomplete combustion. Common urban sources of EC in particulate matter include both mobile sources (diesel-powered buses, cars, and trucks) and point sources (incinerators, power plants and home heating units). The State of Florida operates environmental monitoring stations in selected municipalities around the state. At these stations, which were sited according to EPA requirements², Total Suspended Particulate (TSP) samples were collected using the accepted methods.³ These samples were suitable for EC analysis. Samples collected in the Tampa Bay region in 199b and 1991 were analyzed for EC content using reflectance spectroscopy. EC concentrations were calculated in micrograms per cubic meter (μg/m³).     

Methane in the Atmosphere

Methane is present in the troposphere with a volume concentration of about 1.5 ppm. Estimates of Koyama (1963) indicate a predominantly biological origin with a total production rate of about 2.7 × 10¹⁴ g CH₄/yr. From that he estimated the atmospheric lifetime of methane to be around 20 years. Measurements of the C-l4 in methane by Libby and later by Bainbridge, et al. (1961 ) gave a C-l4 content of 75% of recent wood and, therefore, confirm the predominant biological origin, the addition of inactive CH; from industrial sources being only about 25%. Much less is known about sinks of CH₄. Cadle (1966) reported fairly high destruction rates by atomic O, a reaction which should be important at high altitude. Bainbridge (1966) indeed reports a decrease in the measured methane concentration above the tropopause. He, however, considers this decrease too small to account for the destruction rate of 20 years estimated by Koyama. Our measurements on air samples collected on aircraft flights at various altitudes show a high variability of the CH₄ content both with time and altitude.     

PANs in the Atmosphere

The types of PANs and PBzNs present or possibly present in the ambient atmosphere are discussed. Biological activities of the PANs and PBzNs are briefly considered. The concentration and composition of PANs in the atmosphere are discussed and calculations made of the production of RGO radicals from precursor alkanes, alkenes and aromatic hydrocarbons present in the atmosphere. Lifetimes of PANs are estimated, and the effects of transport on the composition of PANs is evaluated.     

Particulate Emission in Corn Drying

Particulate generation and emission from commercial cross flow driers was sampled in three corn drying seasons. Emission from a pilot scale model was measured in one season. Emission rates along the exhaust side of the drying columns were determined. The particulate was analyzed for size distribution and nutrient content.     

Field Measurements of Particulate Matter Emissions,Carbon Monoxide,and Exhaust Opacity from Heavy-Duty Diesel Vehicles

ABSTRACT

Diesel particulate matter (PM) is a significant contributor to ambient air PM₁₀ and PM_2.5 particulate levels. In addition, recent literature argues that submicron diesel PM is a pulmonary health hazard. There is difficulty in attributing PM emissions to specific operating modes of a diesel engine, although it is acknowledged that PM production rises dramatically with load and that high PM emissions occur during rapid load increases on turbocharged engines. Snap-acceleration tests generally identify PM associated with rapid transient operating conditions, but not with high load. To quantify the origin of PM during transient engine operation, continuous opacity measurements have been made using a Wager 650CP full flow exhaust opacity meter. Opacity measurements were taken while the vehicles were operated over transient driving cycles on a chassis dynamometer using the West Virginia University (WVU) Transportable Heavy Duty Vehicle Emissions Testing Laboratories. Data were gathered from Detroit Diesel, Cummins, Caterpillar, and Navistar heavy-duty (HD) diesel engines. Driving cycles used were the Central Business District (CBD) cycle, the WVU 5-Peak Truck cycle, the WVU 5-Mile route, and the New York City Bus (NYCB) cycle. Continuous opacity measurements, integrated over the entire driving cycle, were compared to total integrated PM mass. In addition, the truck was subjected to repeat snap-acceleration tests, and PM was collected for a composite of these snap-acceleration tests. Additional data were obtained from a fleet of 1996 New Flyer buses in Flint, MI, equipped with electronically controlled Detroit Diesel Series 50 engines. Again, continuous opacity, regulated gaseous emissions, and PM were measured. The relationship between continuous carbon monoxide (CO) emissions and continuous opacity was noted. In identifying the level of PM emissions in transient diesel engine operation, it is suggested that CO emissions may prove to be a useful indicator and may be used to apportion total PM on a continuous basis over a transient cycle. The projected continuous PM data will prove valuable in future mobile source inventory prediction.     

Characterization of Activated Carbon Fiber Filters for Pressure Drop,Submicrometer Particulate Collection,and Mercury Capture

ABSTRACT

The use of activated carbon fiber (ACF) filters for the capture of particulate matter and elemental Hg is demonstrated. The pressure drop and particle collection efficiency characteristics of the ACF filters were established at two different face velocities and for two different aerosols: spherical NaCl and combustion-generated silica particles. The clean ACF filter specific resistance was 153 kg m^-2 sec^-1. The experimental specific resistance for cake filtration was 1.6 × 10⁶ sec^-1 and 2.4 × 10⁵ sec^-1 for 0.5- and 1.5-μm mass median diameter particles, respectively. The resistance factor R was approximately 2, similar to that for the high-efficiency particulate air filters. There was a discrepancy in the measured particle collection efficiencies and those predicted by theory. The use of the ACF filter for elemental Hg capture was illustrated, and the breakthrough characteristic was established. The capacity of the ACF filter for Hg capture was similar to other powdered activated carbons.     

Atmosphere and agriculture in the new millennium

Effects of changing climate (CO(2), O(3), aerosols, UV-B radiation, temperature and precipitation) on crops are predominantly based on univariate studies. Limited bivariate studies suggest rising CO(2) levels would be beneficial to crops but may be offset by adverse O(3) effects. Elevated UV-B and ambient crop yields are difficult to project due also to limited research. Climate warming concerns, using average daily temperatures may be less important than the effects of rising nocturnal temperatures on crop growth. Traditional approaches of examining air pollutant-induced visible foliar injury or the effects of single air pollutants on crop productivity need to be redirected to the analysis of integrated holistic systems. In that context, present and future agriculture in India and the USA are compared.     

Particulate organic matter in the sea: the composition conundrum

As organic matter produced in the euphotic zone of the ocean sinks through the mesopelagic zone, its composition changes from one that is easily characterized by standard chromatographic techniques to one that is not. The material not identified at the molecular level is called "uncharacterized". Several processes account for this transformation of organic matter: aggregation/disaggregation of particles resulting in incorporation of older and more degraded material; recombination of organic compounds into geomacromolecules; and selective preservation of specific biomacromolecules. Furthermore, microbial activities may introduce new cell wall or other biomass material that is not easily characterized, or they may produce such material as a metabolic product. In addition, black carbon produced by combustion processes may compose a fraction of the uncharacterized organic matter, as it is not analyzed in standard biochemical techniques. Despite these poorly-defined compositional changes that hinder chemical identification, the vast majority of organic matter in sinking particles remains accessible to and is ultimately remineralized by marine microbes.     

Characterization of Particulate Matter in California

ABSTRACT

The size, composition, and concentration of particulate matter (PM) vary with location and time. Several monitoring/sampling programs are operated in California to characterize PM less than 2.5 and 10 µm in aerodynamic diameter (PM_2.5 and PM₁₀). This paper presents a broad summary of the spatial and temporal variations observed in ambient PM_2.5 and PM₁₀ concentrations in California. Many areas that have high PM₁₀ concentrations also have relatively high PM_2.5 concentrations, and data indicate that a significant portion of the PM₁₀ air quality problem is caused by PM_2.5. To develop effective plans for attaining the ambient PM standards, improved understanding of these unique problems is needed. Since 1989, pollution control efforts—whether specifically targeted for particulate matter or indirectly via controls on gaseous emissions—have caused annual average PM_2.5 and PM₁₀ concentrations to decline at most sites in California.     

Elemental analysis of airborne particulates in Chile

Aerosol samples collected in three characteristic Chilean cities-including urban and remote zones-have been analyzed by the PIXE spectroscopic technique. Elemental composition, total suspended particulate matter (TSP), particle size distribution, and the peculiar geographic and meteorological parameters have been included in this study. Santiago--the polluted capital of Chile--registered high TSP indexes and important amounts of hazardous elements in air such as S, V, Cr, Zn, Br and Pb. The atmosphere of Antofagasta city showed marine and mineral activity influence. Results from Chillán city are similar to those from rural environments. Protons and deuterons-provided by the isochronous cyclotron of the University of Chile-were used to excite X-ray radiation from the sample. Signals were processed by an energy dispersive detection system, including a cryogenic Si(Li) detector, electronic for pulse amplification and an analog to digital converter. The absolute elemental concentration of the particulate matter in air was obtained through a fundamental parameter equation. Samples consist of particulate material collected directly on Nuclepore filters or deposited over Kapton foils. Typical elements analyzed were Mg, Al, Si, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Cu, Zn, As, Br and Pb.     

Predicting the Performance of Particulate Control Equipment

A new probabilistic modeling environment is described which allows the explicit and quantitative representation of the uncertainties inherent in new environmental control processes for SO₂ and NO_x removal. Stochastic analyses provide additional insights into the uncertainties in process performance and cost not possible with conventional deterministic or sensitivity analysis. Applications of the probabilistic modeling framework are illustrated via an analysis of the performance and cost of the fluidized bed copper oxide process, an advanced technology for the control of SO₂ and NO_x emissions from coal-fired power plants. An engineering model of a conceptual commercial-scale system provides the basis for the analysis. The model also captures interactions between the power plant, the SO₂/NO_x removal process, and other components of the emission control system. Results of the analysis address payoffs from process design improvements; the dependence of system cost on process design conditions and the availability of byproduct markets; and the likelihood that the advanced process will yield cost savings relative to conventional technology. The implications of case study results for research planning and comparisons with alternative systems also are briefly discussed.     

Particulate Air Pollution In the United States

A study was conducted to identify, characterize, and quantify the national particulate air pollution problem from stationary sources. Particulate emissions from stationary sources were determined from data on emission factors, grain loadings, and material balances. The principal method used for establishing the tonnage emitted by an industry utilized uncontrolled emission factors. Total tonnage emitted by a given industry was calculated from four quantities: (1) an emission factor for the uncontrolled source; (2) the total tonnage processed per year by the industry; (3) the efficiency of control equipment used; and (4) the percentage of production capacity equipped with control devices.

Particulate emissions from stationary sources in the United States currently total approximately 18 X 10⁶ ton/yr. The major stationary sources of particulates include electric power generation plants, the crushed stone industry, the forest products industry, agriculture and related operations, the cement industry, and the iron and steel industry.

Three methods were developed to project the total quantity of particulate pollutants emitted up to the year 2000. In making these forecasts, these factors were considered (1) changes in production capacity; (2) improvements in control devices; and (3) regulatory action to enforce installation of control equipment.

These forecasts indicate that particulate emissions can be reduced from the current level of 18 X 10⁶ ton/yr to 3 X 10⁶ ton/yr by 2000 based on the most optimistic forecast. The projections also suggest that major reductions of particulate matter will most likely occur by installation of control equipment on uncontrolled sources and by shifts to more efficient types of collection equipment on existing controlled sources.     

Long Range Cloud Diffusion in the Lower Atmosphere

Previous attempts to measure heavy metals in air are discussed with particular reference to lead. A polarographic method was developed for lead in air samples taken on glass fiber sheet. Using this method, the distribution of lead across the glass fiber sheet was investigated, and within experimental error, found to be uniform. Air samples from 18 Ontario cities, previously analyzed for benzo [a]pyrene content were analyzed.