Analysis of Aerosolized Particulates of Feedyards Located in the Southern High Plains of Texas

The objective of this study was to quantify, size, and examine the composition of particulates found in ambient aerosolized dust of four large feedyards in the Southern High Plains. Ambient air samples (concentration of dust) were collected upwind (background) and downwind of the feedyards. Aerosolized particulate samples were collected using high volume sequential reference ambient air samplers, PM ₁₀ and PM _2.5 , laser strategic aerosol monitors, cyclone air samplers, and biological cascade impactors. Weather parameters were monitored at each feedyard. The overall (main effects and estimable interactions) statistical (P < 0.0001) general linear model statement (GLM) for PM ₁₀ data showed more concentration of dust (μg/m ³ of air) downwind than upwind and more concentration of dust in the summer than in the winter. PM _2.5 concentrations of dust were comparable for 3 of 4 feedyards upwind and downwind, and PM _2.5 concentrations of dust were lower in the winter than in the summer. GLM (P < 0.0001) data for cascade impactor (all aerobic bacteria, Enterococcus spp, and fungi) mean respirable and non-respirable colony forming units (CFU) were 676 ± 74 CFU/m ³ , and 880 ± 119 CFU/m ³ , respectively. The PM ₁₀ geometric mean size (±GSD) of particles were analyzed in aerosols of the feedyards (range 1.782 ± 1.7 μm to 2.02 ± 1.74μm) and PM _2.5 geometric mean size particles were determined (range 0.66 ± 1.76 μm to 0.71 ± 1.71 μm). Three of 4 feedyards were non-compliant for the Environmental Protection Agency (EPA) concentration standard (150 μg/m ³ /24 h) for PM ₁₀ particles. This may be significant because excess dust may have a negative impact on respiratory disease.     

DESIGN AND EXPERIMENTAL CHARACTERIZATION OF A PM1 AND A PM2.5 PERSONAL SAMPLER

This paper presents the development, laboratory and field evaluation of two personal particle samplers (PPS). Both samplers operate at a flow rate of 4 l min^-1, and collect particles smaller than 1.0 and 2.5 μm in aerodynamic diameter, respectively, on 3.7 cm Teflon filters. In each sampler, particles larger than 2.5 or 1.0 μm are retained by impaction onto a coated porous metal disk, which minimizes particle bounce. Using the substrates without any coating results in a substantial reduction of the collection efficiency for particles larger than the 50% cutpoint of the sampler. Particle losses in each sampler are quite low (e.g., on the order of 10% or less) and do not depend significantly on aerodynamic particle diameter. Both samplers display sharp particle cut characteristics, with the ratio of the aerodynamic particle diameter corresponding to 84% collection efficiency to the 50% cutpoint being approximately 1.18 and 1.27 for the PM₁ and the PM_2.5 samplers, respectively. Field tests showed that the mass, sulfate and nitrate concentrations measured by the PM_2.5 PPS and a collocated PM_2.5 Personal Exposure Monitor (PEM) agreed within 10% or less. Such agreement, however, was not observed between the PM_2.5 PPS and the Harvard/EPA Annular Denuder System (HEADS), with the HEADS nitrate concentrations being on the average higher by a factor of 2.1. The particle mass, sulfate and nitrate concentrations obtained with a modified MOUDI sampler collecting all particles smaller than 1 μm in aerodynamic diameter on a filter and the PM₁ PPS were also in very good agreement (e.g., within 7% or less). The two personal particle samplers will be used in field studies in different locations of the U.S. to provide better estimates of human exposures to exclusively particles of the accumulation mode. (e.g., without incorporating the contribution of the coarse mode).     

PM1.0 and PM2.5 Characteristics in the Roadside Environment of Hong Kong

Daily mass concentrations of PM _1.0 (particles less than 1.0 μm in diameter), PM _2.5 (particles less than 2.5 μm in diameter), organic carbon (OC), and elemental carbon (EC) were measured from January through May 2004 at a heavily trafficked sampling site in Hong Kong (PU). The average concentrations for PM _1.0 and PM _2.5 were 35.9 ± 12.4 μ g cm ^{? 3} and 52.3 ± 18.3 μ g cm ^{? 3} . Carbonaceous aerosols were the dominant species in fine particles, accounting for ～ 45.7% of PM _1.0 and ～ 44.4% of PM _2.5 . During the study period, seven fine-particle episodes occurred, due to the influence of long-range transport of air masses from mainland China. PM _1.0 and PM _2.5 responded in similar ways; i.e., with elevated mass and OC concentrations in those episode days. During the sampling period, PM _1.0 OC and EC generally behaved similarly to the carbonaceous aerosols in PM _2.5 , regardless of seasonal variations and influence by regional pollutions. The low and relatively constant OC/EC ratios in PM _1.0 and PM _2.5 indicated that vehicular emissions were major sources of carbonaceous aerosols. PM _1.0 and PM _2.5 had the same dominant sources of vehicular emissions in winter, while in spring PM _2.5 was more influenced by PM _{1 ? 2.5} (particles 1–2.5 μ m in diameter) that did not form from vehicle exhausts. Therefore, PM _1.0 was a better indicator for vehicular emissions at the Roadside Station.     

Investigation of Cut-Off Sizes and Collection Efficiencies of Portable Microbial Samplers

This research investigated the physical collection efficiencies and cut-off sizes of SMA MicroPortable, BioCulture, Microflow, Microbiological Air Sampler (MAS-100), Millipore Air Tester (MAT), SAS Super 180, and RCS High Flow portable microbial samplers when collecting Polystyrene Latex particles ranging from 0.5 to 9.8 μm in aerodynamic size. Traditional collection efficiency measurements often directly compare particle concentrations upstream and downstream of the sampler without considering the particle losses. Here, we developed a new approach which tests collection efficiencies of the sampler with and without agar collection plate loaded. This method thus allows estimating the effective collection efficiency, i.e., the fraction of incoming particles deposited onto the agar collection medium only. The experimental cut-off sizes, or d ₅₀, of the investigated samplers ranged from 1.2 μm for the RCS High Flow, 1.7 μm for the MAS-100, 2.1 μm for SAS Super 180, to 2.3 μm for MAT; for other three samplers they were close to or above 5 μm. In most cases the theoretical d ₅₀ was lower than the experimental value, which was likely due to the dissipation of impactor jets and the influence of cross-flow in the multi-nozzle impactors. For most samplers, we observed a notable difference between the collection efficiency obtained by the traditional measurement method and the effective collection efficiency. In general, all samplers collected 10% or less of 0.5 μm particles onto the agar medium. This study indicates that the use of most of the tested bioaerosol samplers may result in a substantial underestimation of bacterial concentrations, especially of single bacterial cells with diameter 0.5–1.0 μm. On the other hand, most of the investigated samplers would be more efficient when collecting larger fungal spores.     

Characterization of the Gent Stacked Filter Unit PM10 Sampler

ABSTRACT

An integral part of several International Atomic Energy Agency sponsored coordinated research programmes involving the sampling and analysis of ambient airborne particules was the development of a PM₁₀ sampler. Each participant was provided with such a sampler so that comparable samples would be obtained by each of the participating groups. Thus, in order to understand the characteristics of this sampler, we undertoke several characterization studies in which we examined the aerodynamic collection characteristics of the impactor inlet and the reproducibility of the sample mass collection. One of the samplers machined in Belgium was compared with one built from the same design in the U.S. and comparable results were obtained. The sampler was operated side-by-side with a commercial PM₁₀ beta gauge and an IMPROVE-design 2.5 μm cut-point cyclone. Although the sampler was not wind tunnel tested as required for certification as a reference sampler, it does provide a collection efficiency that generally follows the guidelines for a PM₁₀ sampler.     

Development and Evaluation of a High-Volume Aerosol-into-Liquid Collector for Fine and Ultrafine Particulate Matter

This study presents a novel high-volume aerosol-into-liquid collector, developed to provide concentrated slurries of fine and/or ultrafine particulate matter (PM) to be used for unattended, in situ measurements of PM chemistry and toxicity. This system operates at 200 liters per minute (L/min) flow and utilizes the saturation–condensation, particle-to-droplet growth component of the versatile aerosol concentration enrichment system (VACES), growing fine or ultrafine PM to 3–4-μm droplets, in conjunction with a newly designed impactor, in which grown particles are collected gradually forming highly concentrated slurries. Laboratory evaluation results indicated an excellent overall system collection efficiency (over 90%) for both monodisperse and polydisperse particles in the range of 0.01 to 2 μm. Field evaluations illustrated that overall a very good agreement was obtained for most PM_2.5 species between the new aerosol collection system and the VACES/BioSampler tandem as well as filter samplers operating in parallel. Very good agreement between the new system and the VACES/BioSampler was also observed for reactive oxygen species (ROS) in ambient PM_2.5 samples, whereas lower ROS values were obtained from the water extracts of the filter, likely due to incomplete extraction of water insoluble redox active species collected on the filter substrate. Moreover, the field tests indicated that the new aerosol collection system could achieve continuous and unattended collection of concentrated suspensions for at least 2 to 3 days without any obvious shortcomings in its operation. Both laboratory and field evaluations of the high-volume aerosol-into-liquid collector suggest that this system is an effective technology for collection and characterization of ambient aerosols.

Copyright 2013 American Association for Aerosol Research     

Airborne Particle Generation Through Acoustic Ejection of Particles-In-Droplets

This article reports a method to produce airborne particles by generating uniformly sized droplets that contain particles, where the droplets are made with an acoustic ejector that does not need any small orifice or nozzle which might become clogged. We demonstrate stable and continuous ejection for more than 10 minutes of 14-μ m droplets containing 1-μ m polystyrene latex (PSL) particles at a concentration of 1% solids. There was no indication of clogging. We have demonstrated ejection of droplets containing PSL at rates up to 3,000 droplets/s (90,000 1-μ m-PSL particles/s). This method should produce, at a known rate, (1) uniform particles of known volume when the particles are soluble in the liquid and/or (2) particles with a statistical distribution (e.g., Poisson distribution) when the particles are aggregates of primary particles. The method should be useful for aerosol generation systems requiring no volatile organic compounds (VOC).     

Reducing Particle Bounce and Loading Effect for a Multi-Hole Impactor

Aerosol sampling is used to evaluate the health hazards associated with particles deposited in the human breathing system. Impactors, which are extensively employed as aerosol samplers, have low collection efficiency because of particle bounce. The impaction plate is typically coated with oil or grease to prevent particle bounce. However, such coating materials cannot sustain long-term heavy particle loading.

In this study, the impaction plate was recessed, forming a cavity filled with Trypticase Soy Agar (TSA) to reduce particle bounce and re-entrainment. An ultrasonic atomizing nozzle was employed to generate challenge aerosols. An Aerodynamic Particle Sizer (APS) was utilized to measure the number concentrations and the size distributions upstream and downstream of the size-selective devices. A multi-hole impactor and Personal Environmental Monitor PM _2.5 (PEM–PM _2.5 ) were used to evaluate particle bounce and heavy particle loading. Liquid type-Dioctyl phthalate (DOP), soluble solid type-potassium sodium tartrate tetrahydrate (PST) and insoluble solid type-polymethyl methacrylate (PMMA) were investigated, as were different impaction surfaces/surface combinations. The multi-hole impactor coated with silicone oil was compared with a TSA-filled plate. Laboratory results demonstrate that the solid PST particles bounced off the TSA-filled plate less than off the silicone-coated aluminum plate. This study also used a 700-μm-thick layer of silicone oil to prevent TSA dehydration. The experimental results revealed that the silicone-TSA double layer minimized PST particle bounce during the two-hour heavy sampling (mass concentration was around 7.22 mg/m ³ ). Moreover, the PEM-PM _2.5 impactor yielded consistent results when the silicone-TSA double layer method was used. These results are useful for designing bounce-free impaction substrates during heavy load sampling.     

A Shelter to Protect a Passive Sampler for Coarse Particulate Matter,PM10 − 2.5

This work designed and tested a shelter to protect a passive sampler for measuring coarse particulate matter, PM _{10 ? 2.5} . The shelter protects the sampler from precipitation and reduces the effects of wind on the deposition of particles to its collection surface. Six shelters were tested in a wind tunnel at three wind speeds: 2, 8, and 24 km hr ^?1 . Shelter performance was expressed as the ratio of PM _{10 ? 2.5} measured with the passive samplers to that measured with a filter-based dichotomous sampler. For most shelters, the PM _{10 ? 2.5} ratio averaged across wind speeds was well above one (2.4 to 8.5) and was generally dependent on wind speed. However, the PM _{10 ? 2.5} ratio for one shelter, the Flat Plates shelter, was 1.04 with substantially less effect on particle deposition from wind speed. Eight week-long field tests were conducted to compare PM _{10 ? 2.5} measured with a passive sampler installed in a Flat Plates shelter to that measured with a collocated filter-based dichotomous sampler. In these tests, the mean PM _{10 ? 2.5} ratio was 1.29. The linear relationship between PM _{10 ? 2.5} measured passively to that measured with the filter-based sampler had a Pearson correlation coefficient of 0.97 and was not significantly affected by the addition of weekly mean wind speed (p = 0.35). Although temperature was significant in this regression model (p = 0.02), it only improved the relationship marginally. The passive sampler in a Flat Plates shelter offers an inexpensive means to assess ambient PM _{10 ? 2.5} without on-site measurement of wind speed.     

Size-Resolved Concentrations of Particulate Matter and Bioaerosols Inside versus Outside of Homes

Size-resolved airborne particulate matter samples (PM _2.5 , PM ₁₀ , and TSP) collected inside ten northern California homes over four days and one night (9–12 h/sample, spanning a 3.5 week period) were analyzed for protein, endotoxin, and (1 → 3)-β-D-glucan concentrations. Some simultaneous size-resolved outdoor samples were also collected. The associations of residential characteristics and occupant behavior with the indoor airborne levels were investigated. In addition, the relation between these chemical biomarkers and the more traditional culturing approaches was studied. Most of the indoor mass concentration of airborne particles and protein was in the fine fraction (PM _2.5 ), while the mass of airborne endotoxin and (1 → 3)-β-D-glucan was mainly in the coarser fractions (PM _10–2.5 and PM _TSP–10 ). No strong correlations were seen between short-term (3–6 min) culturable bacteria and fungi counts and the corresponding longer-term (9–12 h) biomarker levels. Daytime indoor levels of the biomarkers tended to be higher than outdoors, especially for the PM _10–2.5 fraction, but only in a few cases were the indoor/outdoor relationships statistically significant. Indoor pets were associated with elevated airborne PM and bioaerosols inside homes. Two other factors, wall-to-wall carpet and older houses, also appear to be associated with some elevations in indoor levels.     

Chemical Mass Closure and Chemical Characteristics of Ambient Ultrafine Particles and other PM Fractions

Ambient ultrafine particles (UPs or PM _0.1 ), PM _2.5 and PM ₁₀ were investigated at the roadside of Syuefu road in Hsinchu city and in the Syueshan highway tunnel in Taipei, Taiwan. A SMPS (TSI Model 3936), three Dichotomous samplers (Andersen Model SA-241), and three MOUDIs (MSP Model 110) were collocated to determine the PM number and mass concentrations simultaneously. The filter samples were further analyzed for organic carbon (OC), element carbon (EC), water-soluble ions, and trace elements. The OC artifact was studied and quantified using the quartz behind quartz (QBQ) method for all PM fractions. Taking into account the OC artifact, chemical mass closure (ratio of the reconstructed chemical mass to the gravimetrical mass) of PM _0.1 , PM _2.5 , and PM ₁₀ was then calculated and found to be good. The chemical analysis results of UPs at both sites showed that UPs in the present tunnel was mostly contributed from the vehicle emissions while UPs at the roadside was mainly influenced by urban sources.     

Development and Evaluation of a Continuous Ambient PM2.5 Mass Monitor

A Continuous Ambient Mass Monitor (CAMM) for fine particle mass (PM_2.5) has recently been developed at the Harvard School of Public Health. The principle of this method is based on the measurement of the increase in pressure drop across a membrane filter (Fluoropore^TM) during particle sampling. The monitor consists of a conventional impactor inlet to remove particles larger than 2.5 mu m, a diffusion dryer to remove particle-bound water, a filter tape to collect particles, a filter tape transportation system to allow unassisted sampling, and a data acquisition and control unit. For each sampling period (typically 30- 60 min), a new segment of the filter tape is exposed so that particles remain close to equilibrium with the sample air during their collection. This results in mini mization of volatilization and adsorption artifacts during sampling. Furthermore, since the required flow rate for the fine particle mass monitoring channel is only 0.3 L / min, the relative humidity of the air sample can be easily reduced to 40% or less using a NafionTM diffusion dryer to remove particle-bound water. The CAMM has a detection limit of > 5 mu g / m³ for PM_2.5 concentrations averaged over 1 h. The performance of the newly developed monitor was investigated through laboratory and field studies. Laboratory tests included a calibration of the CAMM using polystyrene latex (PSL) and silica particles. A series of field studies were conducted in 7 cities with presumably different PM_2.5 chemical composition. The 24 1-h CAMM measurements were averaged and compared to Harvard Impactor (HI) 24 h PM_2.5 integrated measurements. Based on 211 valid sampling days, the measurements obtained from the Harvard Impactor and the CAMM were highly correlated (r² = 0.90). The average CAMM-to-HI concentration ratio was 1.07 (+- 0.18).     

PM2.5 and PM10 Mass Measurements in California's San Joaquin Valley

PM _2.5 and PM ₁₀ mass measurements from different sampling systems and locations within California's San Joaquin Valley (SJV) are compared to determine how well mass concentrations from a unified data set can be used to address issues such as compliance with particulate matter (PM) standards, temporal and spatial variations, and model predictions. Pairwise comparisons were conducted among 20 samplers, including four Federal Reference Method (FRM) units, battery-powered MiniVols, sequential filter samplers, dichotomous samplers, Micro-Orifice Uniform Deposit Impactors (MOUDIs), beta attenuation monitors (BAMs), tapered element oscillating microbalances (TEOMs), and nephelometers. The differences between FRM samplers were less than 10 and 20% for 70 and 92% of the pairwise comparisons, respectively. The TEOM, operating at 50°C in this study, measured less than the other samplers, consistent with other comparisons in nitrate-rich atmospheres. PM _2.5 mass measured continuously with the BAM was highly correlated with filter-based PM _2.5 although the absolute bias was greater than 20% in 45% of the cases. Light scattering (B _sp ) was also highly correlated with filter-based PM _2.5 at most sites, with mass scattering efficiencies varying by 10 and 20% for B _sp measured with Radiance Research nephelometers with and without PM _2.5 size-selective inlets, respectively. Collocating continuous monitors with filter samplers was shown to be useful for evaluating short-term variability and identifying outliers in the filter-based measurements. Comparability among different PM samplers used in CRPAQS is sufficient to evaluate spatial gradients larger than about 15% when the data are pooled together for spatial and temporal analysis and comparison with models.     

Sieving of aerosol particles with metal screens

Metal screens with uniform micrometer-sized opening were employed to sieve aerosol particles by suppressing the adhesion of particles smaller than the openings. The collection efficiencies of monodispersed polystyrene latex (PSL) particles were experimentally determined using the metal screens with 1.2, 1.8, 2.5, and 4.2 μm openings at various filtration velocities. The particles smaller than the mesh opening adhered on the metal screen at a low filtration velocity, but the bounce-off of particles on the mesh surface suppressed the adhesion at a high velocity. As a result, we found that the adhesion of PSL particles larger than 0.3 μm mostly suppressed at a filtration velocity higher than 10 m s^?1 and therefore we can sieve aerosol particles according to the opening size of metal screens. We also found that the particle number concentration could be determined by measuring the increase in pressure drop since the clogging of metal screen openings takes place by the individual particles.

© 2016 American Association for Aerosol Research     

Development of a Sharp-Cut Cyclone for Ambient Aerosol Monitoring Applications

Aerosol samplers for ambient PM2.5 are required to possess a steep aerodynamic particle size selection curve, i.e., a 'sharp cut' at 2.5 mu m aerodynamic diameter. For long-term and continuous PM monitors the selector system also requires low maintenance and the ability to operate at high loadings. While a sharp cut is easier to achieve with an impactor-based selector, the other require ments are more easily met with a cyclone. Four alternative PM2.5 selectors were tested against these criteria: two were pre-existing commercial designs and two were novel cyclone prototypes. The main aim of the work was to assess the characteristics of the selectors when clean and under various loading conditions. The aerodynamic size-selection characteristics of the PM2.5 selectors were tested before and after loading with dust, under both laboratory and field conditions. Aerosol penetration measurements were made using an Aerodynamic Particle Sizer. Many repeat tests were performed on two specimens of the Well Impactor Ninety-Six (WINS), two specimens of a novel Sharp-Cut Cyclone (SCC), one member of the GK cyclone family (GK4.39), and one University Research Glass ware (URG) cyclone. Four loadings of the WINS and SCC were made in the laboratory using a narrow-fraction alumina dust. The penetration curves were measured after each loading. Five cumulative outdoor loadings were made by setting up four PM2.5 samplers, two with the WINS and two with the SCC, in a suburban garden during the summer months. The penetration curves were mea sured at weekly intervals after sampling times ranging from 96 to 132 h. Three further cumulative loadings were tested in a similar experiment in a city-center underground car park. When clean, all three PM2.5 size selectors were shown to have 50%penetration (D₅₀) values close to 2.5 mu m, although the penetration curve shape differs for the three selector designs. Under loading the D₅₀ value for both the WINS and SCC fell, with the decrease being largest for the WINS. With high loadings the SCC D₅₀ fell to 2.35 mu m and the WINS D₅₀ fell to 2.15 mu m. The WINS deviation was large enough to potentially lead to under sampling of PM2.5. The SCC cyclone was seen to provide a sharp cut for ambient air sampling applications that is less affected than the WINS by loading. Additionally, the SCC is a dry system whereas the WINS uses an oiled substrate. While the WINS cut point is unlikely to shift to an unacceptable degree during 24 or 96 h sampling periods, it would perform less well than the SCC over extended sampling periods.     

Investigation of inherent and latent internal losses in liquid-based bioaerosol samplers

Previous studies have analyzed collection efficiencies and reaerosolization rates of liquid-based bioaerosol collectors. However, these studies did not analyze latent internal losses in the samplers, i.e., the fraction of the particles that is aerosolized from the collection liquid, attach to the samplers’ inner surfaces and do not leave the sampler via outlet. Here, we investigated the internal losses and reaerosolization rates in BioSampler (SKC Inc., Eighty Four, PA) and AGI-30 (Ace Glass Inc., Vineland, NJ) bioaerosol collectors operated with different amounts of liquid as a function of particle type (polystyrene latex particles of 0.9 and 3.2 μm, B. subtilis bacteria and C. cladosporioides fungal spores), particle concentration (“low” and “high” differing by a factor of 100) and operating time (15 and 30 min). The samplers were filled with sterile deionized water containing known (reference) particle concentrations and were operated in a particle-free atmosphere for 15 or 30 min. The overall particle loss was determined by comparing the concentration of particles remaining in the collection liquid with the reference concentration. The reaerosolization rates were estimated by comparing the concentration of particles collected at each sampler's outlet with the reference concentration. The internal loss was determined as a fraction of particles remaining attached to the inner walls of a sampler, i.e., particles not in the collection liquid and not reaerosolized. All the investigated variables had a statistically significant effect on the overall particle loss, the reaerosolization rate and the internal loss. Averaged for all test conditions, the internal loss for BioSampler with 5 mL liquid, BioSampler with 20 mL liquid and AGI-30 was 37.7%, 29.6% and 22.5%, respectively. The observed reaerosolization rates were rather low and ranged from 0.2% to 6.9%. This study shows that depending on a particular set of sampling conditions a substantial fraction of already collected particles could leave the collection fluid, attach to the inner surfaces of the samplers and not be available for sample analysis thus affecting the accuracy of bioaerosol investigations.     

A Novel Multifilter PM10–PM2.5 Sampler (MFPPS)

A novel multifilter PM₁₀–PM_2.5 sampler (MFPPS) that enables the collection of four PM₁₀ and four PM_2.5 samples simultaneously has been developed and tested. The MFPPS uses a PM₁₀ impactor as the inlet and operates at 33.4 L/min. After the inlet, the aerosol flow is divided half by a Y-type fitting. Half of the flow is directed into four PM₁₀ filter cassettes, while the other half is directed into four PM_2.5 filter cassettes after the aerosols are further classified by a PM_2.5 impactor. An active flow control system consisting of two mass flow controllers (MFCs), one for PM₁₀ and the other for PM_2.5, is used to fix the total flow rate of 16.7 L/min for four PM₁₀ or four PM_2.5 channels based on the ambient pressure and temperature. To ensure flow rate uniformity through each of the four PM₁₀ or four PM_2.5 filter cassettes, an orifice is assembled behind each of the filter cassettes to increase the pressure drop, such that the flow rates of eight sampling lines are nearly equal using just two MFCs. The MFPPS was calibrated in the laboratory for particle collection efficiency curves first. Then, the ambient PM concentrations were compared with those of other two collocated FRM samplers, the dichotomous PM₁₀ and the EPA WINS PM_2.5 sampler in the field study. Calibration results showed the cutoff aerodynamic diameters of the PM₁₀ and PM_2.5 impactors were 9.8 ± 0.1 and 2.5 ± 0.05 μm, respectively. Field comparison results indicated PM₁₀ and PM_2.5 concentrations agreed well with the other two PM samplers.     

Effect of Semivolatile Material on PM 2.5 Measurement by the PM 2.5 Federal Reference Method Sampler at Bakersfield,California

The chemical composition of fine particulate material was determined for samples collected in Bakersfield, CA, during February-March, 1998 using several diffusion denuder samplers, including the PC-BOSS, which measures both semivolatile fine particulate nitrate and organic material. An average of 56% of the fine particulate carbonaceous material was lost from the filters of the Particle Concentrator-Brigham Young University Organic Sampling System (PC-BOSS). A comparable amount of fine particulate semivolatile organic material was also lost from collected particles with single filter samplers, such as the PM 2.5 Federal Reference Method. The fraction of nitrate lost from collected particles was a function of temperature and humidity, with the biggest effect being due to temperature. The fraction of nitrate lost was comparable for conventional annular denuder samplers and the PM 2.5 FRM, averaging 33%. The nitrate loss from particles for the PC-BOSS was smaller, averaging 11%, possibly due to the concentration of particulate material prior to collection with this sampler. The loss of nitrate and semivolatile organic material during sample collection resulted in the PM 2.5 FRM sampler giving PM 2.5 mass that was an average of 30% (7.3 w g/m 3 ) lower than the true value and different from the true value from negligible to 20 w g/m 3 .     

PM10/PM2.5/PM1 Data from a Trichotomous Sampler

ABSTRACT

As part of an effort to determine whether 1 μm or 2.5 μam is the better choice for a new fine particulate matter standard, Professor Virgil A. Marple of the University of Minnesota developed a high volume trichotomous (PM₁₀/PM_2.5 /PM₁) sampler. Two of these samplers were used to obtain particulate matter (PM) samples at a site located in Phoenix, Arizona, from May 1995 through October 1995. All filter samples were analyzed for mass concentrations and a few for elemental and chemical compositions. Relative fractions were determined for PM₁₀, PM_2.5, PM₁, PM_2.5–10, and PM_1–2.5. Calculations were made to evaluate how coarse and fine mode aerosol contributed to the intermediate size range. Results indicated that most of the PM₁₀ in Phoenix was coarse mode PM (windblown dust), which was also a primary contributor to PM₂₅.     

Experimental and Modeling Studies of the Stream-Wise Filter Vibration Effect on the Filtration Efficiency

The stream-wise vibration effect of a fibrous filter is studied experimentally and numerically for the purpose of evaluating filtration efficiency. The particle sizes range from 0.02 to 10 μ m and the face velocity ranges from 3 to 10 cm/s. The vibrational peak velocity also varied from 0 to 50 cm/s. The filtration efficiency for this wide size range is obtained by combining the individual test results for fine particles (0.02 to 0.5 μ m) and large particles (0.5 to 10.0 μ m). For the fine particle experiment, Arizona Road Dust (ARD) test particles are generated by an atomizer after an ultrasonic process and measured by a Scanning Mobility Particle Sizer (SMPS). For the large particle experiment, the test particles are generated by a fluidized bed and measured by an Aerodynamic Particle Sizer (APS). When the particles are generated by the atomizer after ultrasonicating, the majority of the particles are in nano scale without the agglomerates on the large particle surface, while particles generated by the fluidized bed are mostly in micro-scale because many nanoparticles are agglomerated on large particle surface. The filtration efficiency increases with the vibrational peak velocity in the impaction-dominant region (D _p > 0.1 μ m) and diffusion-dominant region (D _p < 0.1 μ m), due to the increased relative velocity between the particle and the filter fiber and the increased diffusion intensity from turbulence around the fiber, respectively. A model for the filter vibration effect is established with a modified Stokes number for the impaction-dominant region and an empirical analysis for the diffusion-dominant region.