Technique for Measuring Dust Collector Efficiency As a Function of Particle Size

With a specially designed generator, producing an aerosol of concentration, chemical composition, and size distribution similar to incinerator aerosols, a scrubber was tested in the laboratory by sampling before and after the collector. Using an Andersen Sampler as a 7 stage cascade impactor the efficiency for 7 different size classes was determined. This technique provides a rapid and simple method for evaluating the performance of a collector as a function of particle size. The multistage impaction classifies the particles according to their aerodynamic behavior. Gravimetric analysis of each stage eliminates the need for tedious counting and sizing.     

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).     

An Aerosol Sampler for Determination of Particle Concentration as a Function of Size and Time

A high flow rate four-stage impacfor was developed for the determination of aerosol concentration as a function of both particle size and time. The unit is very useful for long-term sampling intervals (24 hr) and for sampling very dusty atmospheres. Gas-borne particulate matter is collected out on four rotating drums, each with a collection surface area of about 10 sq in.; this allows a large quantity of materials to be collected without danger of particle build-up and blow-off. A particle size-collection efficiency calibration for the unit is presented together with experimental data on wall losses, surface coatings, and other important operational considerations.     

Fine Particle Collection Efficiency Related to Pressure Drop,Scrubbant and Particle Properties,and Contact Mechanism

Collection efficiencies are shown for control of fine particles in venturi scrubbers (1) as a function of pressure drop, and (2) as a function of throat area and liquid to gas ratio. A relationship of pressure drop to throat area, gas density, throat velocity, and liquid to gas ratio is given and is used to provide a method for estimating efficiency knowing only these scrubber design parameters. The effect of charged particles and of surface active agents on collection efficiency are discussed briefly.     

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.     

Effect of Dust Size Distribution on the Collection Efficiency of Pulse-Jet Fabric Filters

Recent advances in vehicle emission control technology have reduced the effectiveness of the conventional tailpipe test used In inspection and maintenance programs. A different approach Is being followed in Harris County, Texas (Houston area), based on identification and correction of misfuellng and tampering. Misfueling Is being identified by using a lead-sensitive test paper to detect lead deposits in the tailpipe that result from using leaded gasoline. Field tests of this procedure demonstrated that it Is reliable and accurate for the Intended purpose. The data also indicated the need to observe certain precautions to avoid contamination and other potential sources of error. This procedure and other emission-related checks have been added to the annual safety inspections. These tests are conducted on vehicles of 1980 model year and later, by approximately 1150 Inspection stations throughout the county that conduct annual safety Inspections. Experience with the first few months of this program has been excellent.     

On the Minimum Efficiency and the Most Penetrating Particle Size for Fibrous Filters

Equations for predicting the minimum efficiency and most penetrating particle size for fibrous filters have been derived by considering the diffusion and interception mechanisms. The results show that the most penetrating particle size decreases with increasing filtration velocity and with increasing fiber volume fraction, and increases with increasing filter fiber size. The corresponding equation for minimum efficiency has also been derived showing the dependence on filtration velocity, fiber volume fraction, and fiber size. These results have been compared with experimental data and satisfactory agreement has been obtained.     

Effect of Diffusiophoresis and Thermophoresis on the Overall Particle Collection Efficiency of Spray Droplet Scrubbers

The overall particle collection efficiencies of spray scrubbers using monodisperse droplets of 100,500, and 1000 microns diameter were calculated for the cases of evaporating and condensing droplets. The properties of the gas at the inlet to the spray scrubber were maintained constant at 150°F, 100% relative humidity, and 1 atmosphere pressure. At the liquid entrance to the spray scrubber, the water droplet temperature was 50° F for the condensing case and 180° F for the evaporating case. The liquid to gas flow rate ratio for all the calculations was held constant at 4 gal/1000 acf. The gas velocity in the co-current spray tower was 1 ft/sec in the downwind direction. The calculation results show that for the particles in the 0.01 to 10 Mm diameter range, the overall spray scrubber particle collection efficiency is greater with the cooler 50°F water (condensing case) than with the warmer 180°F water (evaporating case). The effect of diffusiophoresis and thermophoresis is noticeable for all the water droplet sizes considered, but is more significant for the larger water droplets. This greater effect for the larger water droplets compared to the smaller droplets is due to the longer existence of the temperature and water vapor concentration gradients between the water droplets and the surrounding gas.     

The Influences of Ambient Particle Composition and Size on Particle Infiltration in Los Angeles,CA, Residences

Abstract

Particle infiltration is a key determinant of the indoor concentrations of ambient particles. Few studies have examined the influence of particle composition on infiltration, particularly in areas with high concentrations of volatile particles, such as ammonium nitrate (NH₄NO₃). A comprehensive indoor monitoring study was conducted in 17 Los Angeles–area homes. As part of this study, indoor/outdoor concentration ratios during overnight (nonindoor source) periods were used to estimate the fraction of ambient particles remaining airborne indoors, or the particle infiltration factor (F_INF), for fine particles (PM_2.5), its nonvolatile (i.e., black carbon [BC]) and volatile (i.e., nitrate [NO₃ ^?]) components, and particle sizes ranging between 0.02 and 10 μm. F_INF was highest for BC (median = 0.84) and lowest for NO₃ ^? (median = 0.18). The low F_INF for NO₃ ^? was likely because of volatilization of NO₃ ^? particles once indoors, in addition to depositional losses upon building entry. The F_INF for PM_2.5 (median = 0.48) fell between those for BC and NO₃ ^?, reflecting the contributions of both particle components to PM_2.5. F_INF varied with particle size, air-exchange rate, and outdoor NO₃ ^? concentrations. The F_INF for particles between 0.7 and 2 μm in size was considerably lower during periods of high as compared with low outdoor NO₃ ^? concentrations, suggesting that outdoor NO₃ ^? particles were of this size. This study demonstrates that infiltration of PM_2.5 varies by particle component and is lowest for volatile species, such as NH₄NO₃. Our results suggest that volatile particle components may influence the ability for outdoor PM concentrations to represent indoor and, thus, personal exposures to particles of ambient origin, because volatilization of these particles causes the composition of PM_2.5 to differ indoors and outdoors. Consequently, particle composition likely influences observed epidemiologic relationships based on outdoor PM concentrations, especially in areas with high concentrations of NH₄NO₃ and other volatile particles.     

Performance of a Pulse-Jet Filter at High Filtration Velocity I. Particle Collection

The fly ash collection characteristics of a pulse-jet fabric filter have been studied. Fly ash penetration was found to decrease as the dust deposit increased from 0 to 60 micrometers in thickness, to increase as face velocity through the bags increased from 5 to 15 cm/s, and to remain relatively constant for particles from 0.3 to 4.0 µm in diameter. Experiments employing chemically tagged fly ash were performed to investigate three dust penetration mechanisms. On resumption of filtering after cleaning, penetration by straight through dust loss declined rapidly from its maximum, reached a minimum, and then increased. Seepage of dust through the fabric was found to be constant throughout the filtration cycle. Dust lost as pinhole plugs increased after cleaning, passed through a maximum, and then declined. The pinholes appeared to open the way for further penetration by the straight through mechanism.     

Measurement of Ultrafine Particle Size Distributions from Coal-, Oil-, and Gas-Fired Stationary Combustion Sources

Abstract

Currently, we have limited knowledge of the physical and chemical properties of emitted primary combustion aerosols and the changes in those properties caused by nucleation, condensation growth of volatile species, and particle coagulations under dilution and cooling in the ambient air. A dilution chamber was deployed to sample exhaust from a pilot-scale furnace burning various fuels at a nominal heat input rate of 160 kW/h^?1 and 3% excess oxygen. The formation mechanisms of particles smaller than 420 nm in electrical mobility diameter were experimentally investigated by measurement with a Scanning Mobility Particle Sizer (SMPS) as a function of aging times, dilution air ratios, combustion exhaust temperatures, and fuel types. Particle formation in the dilution process is a complex mixture of nucleation, coagulation, and condensational growth, depending on the concentrations of available condensable species and solid or liquid particles (such as soot, ash) in combustion exhausts. The measured particle size distributions in number concentrations measured show peaks of particle number concentrations for medium sulfur bituminous coal, No. 6 fuel oil, and natural gas at 40-50 nm, 70-100 nm, and 15-25 nm, respectively. For No. 6 fuel oil and coal, the particle number concentration is constant in the range of a dilution air ratio of 50, but the number decreases as the dilution air ratio decreases to 10. However, for natural gas, the particle number concentration is higher at a dilution air ratio of 10 and decreases at dilution air ratios of 20-50. At a dilution air ratio of 10, severe particle coagulation occurs in a relatively short time. Samples taken at different combustion exhaust temperatures for these fuel types show higher particle number concentrations at 645 K than at 450 K. As the aging time of particles increases, the particles increase in size and the number concentrations decrease. The largest gradient of particle number distribution occurs within the first 10 sec after dilution but shows only minor differences between 10 and 80 sec. The lifetimes of the ultrafine particles are relatively short, with a scale on the order of a few seconds. Results from this study suggest that an aging time of 10 sec and a dilution air ratio of 20 are sufficient to obtain representative primary particle emission samples from stationary combustion sources.     

Filtration of Airborne Particulates by Gravel Filters: I. Initial Collection Efficiency of a Gravel Layer

An equation derived for initial collection of efficiency E₀ of a gravel bed filter predicts that — ln(1 — E₀) is proportional to the thickness of the gravel layer, to the — 5/3 power of the diameter of uniform gravels, and to the — 2/3 power of the Darcy airflow velocity. The experimental data obtained from NH₄CI fume removal from dry air at room temperature by sieved gravel fractions generally supported the equation, except that the effect of mean gravel size was represented by the —1.43 power of the average diameter.     

Characterization of Indoor Particle Sources Using Continuous Mass and Size Monitors

ABSTRACT

A comprehensive indoor particle characterization study was conducted in nine Boston-area homes in 1998 in order to characterize sources of PM in indoor environments. State-of-the-art sampling methodologies were used to obtain continuous PM_2.5 concentration and size distribution particulate data for both indoor and outdoor air. Study homes, five of which were sampled during two seasons, were monitored over week-long periods. Among other data collected during the extensive monitoring efforts were 24hr elemental/organic carbon (EC/OC) particulate data as well as semi-continuous air exchange rates and time-activity information.

This rich data set shows that indoor particle events tend to be brief, intermittent, and highly variable, thus requiring the use of continuous instrumentation for their characterization. In addition to dramatically increasing indoor PM₂₅ concentrations, these data demonstrate that indoor particle events can significantly alter the size distribution and composition of indoor particles. Source event data demonstrate that the impacts of indoor activities are especially pronounced in the ultrafine (d_a < 0.1 um) and coarse (2.5 < d_a < 10 |um) modes. Among the sources of ultrafine particles characterized in this study are indoor ozone/terpene reactions. Furthermore, EC/OC data suggest that organic carbon is a major constituent of particles emitted during indoor source events. Whether exposures to indoor-generated particles, particularly from large short-term peak events, may be associated with adverse health effects will become clearer when biological mechanisms are better known.     

Collection and analysis of Nicotine as a marker for environmental tobacco smoke

Nicotine is a potential marker for environmental tobacco smoke (ETS) because it is unique to tobacco smoke and is a major constituent of the smoke. An air sampling method is presented which efficiently collects both particulate and vapor phase nicotine. Two filters are assembled in tandem in a personal sampling cassette. The first filter collects total or size fractional particules and the second is treated with sodium bisulfate to collect vapor phase nicotine and nicotine which has volatilized from the paniculate material collected on the first filler. The nicotine is then desorbed from the filters and analyzed by gas chromatography with nitrogen sensitive detection. The sampling method was evaluated in an environmental chamber under controlled conditions of temperature, humidity, ventilation and smoking rate. It was then employed in a field study of particulate exposures of railroad office workers and railroad mechanics to determine the portion of the particulate exposure attributable to environmental tobacco smoke. The method was found to be efficient and sensitive for the determination of nicotine levels in air.     

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.     

Lynx Body Size in Norway is Related to its Main Prey (Roe Deer) Density,Climate, and Latitude

We studied the effect of various factors on body size variation of the Eurasian lynx in Norway, using data from 374 lynx collected between 1960 and 1976 and whose locality of capture, year of birth, sex, and age were known. Body size of lynx in Norway was mainly affected by sex and age. Female skull size (and by implication body size) was also positively affected by the availability of its main prey (roe deer) and by latitude, and negatively by the North Atlantic Oscillation (NAO). Male size was not affected by any of the environmental factors examined. We interpret the effects of NAO and latitude on body size through their effect on the local climate and particularly snow conditions. We suggest that females are more sensitive to environmental factors than males.     

Atmospheric phosphorus deposition at a montane site: Size distribution,effects of wildfire,and ecological implications

The dry deposition of atmospheric particulate matter can be a significant source of phosphorus (P) to oligotrophic aquatic ecosystems, including high-elevation lakes. In this study, measurements of the mass concentration and size distribution of aerosol particles and associated particulate P are reported for the southern Sierra Nevada, California, for the period July–October, 2008. Coarse and fine particle samples were collected with Stacked Filter Units and analyzed for Total P (TP) and inorganic P (IP) using a digestion-extraction procedure, with organic P (OP) calculated by difference. Particle size-resolved mass and TP distributions were determined concurrently using a MOUDI cascade impactor. Aerosol mass concentrations were significantly elevated at the study site, primarily due to transport from offsite and emissions from local and regional wildfires. Atmospheric TP concentrations ranged from 11 to 75 ng m^?3 (mean = 37 ± 16 ng m^?3), and were typically dominated by IP. Phosphorus was concentrated in the coarse (>1 μm diameter) particle fraction and was particularly enriched in the 1.0–3.2 μm size range, which accounted for 30–60% of the atmospheric TP load. Wildfire emissions varied widely in P content, and may be related to fire intensity. The estimated dry depositional flux of TP for each daily sampling period ranged between 7 and 118 μg m^?2 d^?1, with a mean value of 40 ± 27 μg m^?2 d^?1. Relative rates of dry deposition of N and P in the Sierra Nevada are consistent with increasing incidence of N limitation of phytoplankton growth and previously observed long-term eutrophication of lakes.     

Sorption of Pesticides on Kaolinite and Montmorillonite as a Function of Hydrophilicity

Pesticides and other organic species are adsorbed by soil via different mechanisms, with bond strengths that depend on the properties of both the soil and the pesticide. Since the clay fraction in soil is a preferential sorbent for organic matter, reference kaolinite and montmorillonite are useful models for studying the mechanism and the strength of sorption. This paper presents the results of batch experiments to investigate the interactions of kaolinite KGa-1 and montmorillonite SWy-1 with the following pesticides and organic species resulting from the natural degradation of pesticides in the environment: atrazine (1-chloro-3-ethylamino-5-isopropylamino-2,4,6-triazine), simazine (1-chloro-3,5-bisethylamino-2,4,6-triazine), diuron [1,1-dimethyl-3-(3,4-dichlorophenyl)urea], aniline, 4-chlorophenol, 2,4-dichlorophenol, and 2,4,6-trichlorophenol. Each of these chemicals has different hydrophilicity. Systems containing 2.0 g of clay were put in contact with 100.0 mL of solutions of the pesticides at known concentration ranging from 1.0 to 5.0 mg/L, and the amount of solute adsorbed was evaluated through RP-HPLC analysis of the pesticide still present in the aqueous suspension. To test for electrostatic interactions between the clay surface and the pesticides, potentiometric titration was used to determine the permanent surface charge of clays. Experiments were performed at different pH values. The results indicate that, for the chemicals studied, neutral molecules are preferentially retained relative to ionized ones, and that montmorillonite is a more effective sorbent than kaolinite.     

Comparison of the Particle Size Distribution of Heavy-Duty Diesel Exhaust Using a Dilution Tailpipe Sampler and an In-Plume Sampler during On-Road Operation

ABSTRACT

Originally constructed to develop gaseous emission factors for heavy-duty diesel trucks, the U.S. Environmental Protection Agency's (EPA) On-Road Diesel Emissions Characterization Facility has been modified to incorporate particle measurement instrumentation. An electrical low-pressure impactor designed to continuously measure and record size distribution data was used to monitor the particle size distribution of heavy-duty diesel truck exhaust. For this study, which involved a high-mileage (900,000 mi) truck running at full load, samples were collected by two different methods. One sample was obtained directly from the exhaust stack using an adaptation of the University of Minnesota's air-ejector-based mini-dilution sampler. The second sample was pulled from the plume just above the enclosed trailer, at a point ~11 m from the exhaust discharge. Typical dilution ratios of about 300:1 were obtained for both the dilution and plume sampling systems. Hundreds of particle size distributions were obtained at each sampling location. These were compared both selectively and cumulatively to evaluate the performance of the dilution system in simulating real-world exhaust plumes. The data show that, in its current residence-time configuration, the dilution system imposes a statistically significant bias toward smaller particles, with substantially more nanoparticles being collected than from the plume sample.     

Comparison of Particle Size Distributions and Elemental Partitioning from the Combustion of Pulverized Coal and Residual Fuel Oil

ABSTRACT

U.S. Environmental Protection Agency (EPA) research examining the characteristics of primary PM generated by the combustion of fossil fuels is being conducted in efforts to help determine mechanisms controlling associated adverse health effects. Transition metals are of particular interest, due to the results of studies that have shown cardiopulmonary damage associated with exposure to these elements and their presence in coal and residual fuel oils. Further, elemental speciation may influence this toxicity, as some species are significantly more water-soluble, and potentially more bio-available, than others. This paper presents results of experimental efforts in which three coals and a residual fuel oil were combusted in three different systems simulating process and utility boilers. Particle size distributions (PSDs) were determined using atmospheric and low-pressure impac-tion as well as electrical mobility, time-of-flight, and light-scattering techniques. Size-classified PM samples from this study are also being utilized by colleagues for animal instillation experiments.

Experimental results on the mass and compositions of particles between 0.03 and >20 μm in aerodynamic diameter show that PM from the combustion of these fuels produces distinctive bimodal and trimodal PSDs, with a fine mode dominated by vaporization, nucleation, and growth processes. Depending on the fuel and combustion equipment, the coarse mode is composed primarily of unburned carbon char and associated inherent trace elements (fuel oil) and fragments of inorganic (largely calcium-alumino-silicate) fly ash including trace elements (coal). The three coals also produced a central mode between 0.8- and 2.0-μm aerodynamic diameter. However, the origins of these particles are less clear because vapor-to-particle growth processes are unlikely to produce particles this large.

Possible mechanisms include the liberation of micron-scale mineral inclusions during char fragmentation and burnout and indicates that refractory transition metals can contribute to PM <2.5 μm without passing through a vapor phase. When burned most efficiently, the residual fuel oil produces a PSD composed almost exclusively of an ultrafine mode (~0.1 μm). The transition metals associated with these emissions are composed of water-soluble metal sulfates. In contrast, the transition metals associated with coal combustion are not significantly enriched in PM <2.5 μm and are significantly less soluble, likely because of their association with the mineral constituents. These results may have implications regarding health effects associated with exposure to these particles.