Evaluating the capabilities of Aerosol-to-Liquid Particle Extraction System (ALPXS)/ICP-MS for monitoring trace metals in indoor air

This study investigates the application of the Aerosol-to-Liquid Particle Extraction System (ALPXS), which uses wet electrostatic precipitation to collect airborne particles, for multi-element indoor stationary monitoring. Optimum conditions are determined for capturing airborne particles for metal determination by inductively coupled plasma–mass spectrometry (ICP-MS), for measuring field blanks, and for calculating limits of detection (LOD) and quantification (LOQ). Due to the relatively high flow rate (300 L min^?1), a sampling duration of 1 hr to 2 hr was adequate to capture airborne particle-bound metals under the investigated experimental conditions. The performance of the ALPXS during a building renovation demonstrated signal-to-noise ratios appropriate for sampling airborne particles in environments with elevated metal concentrations, such as workplace settings. The ALPXS shows promise as a research tool for providing useful information on short-term variations (transient signals) and for trapping particles into aqueous solutions where needed for subsequent characterization. As the ALPXS does not provide size-specific samples, and its efficiency at different flow rates has yet to be quantified, the ALPXS would not replace standard filter-based protocols accepted for regulatory applications (e.g., exposure measurements), but rather would provide additional information if used in conjunction with filter based methods.

ImplicationsThis study investigates the capability of the Aerosol-to-Liquid Particle Extraction System (ALPXS) for stationary sampling of airborne metals in indoor workplace environments, with subsequent analysis by ICP-MS. The high flow rate (300 L/min) permits a short sampling duration (< 2 hr). Results indicated that the ALPXS was capable of monitoring short-term changes in metal emissions during a renovation activity. This portable instrument may prove to be advantageous in occupational settings as a qualitative indicator of elevated concentrations of airborne metals at short time scales.     

The use of wind fields in a land use regression model to predict air pollution concentrations for health exposure studies

A methodology is developed to include wind flow effects in land use regression (LUR) models for predicting nitrogen dioxide (NO₂) concentrations for health exposure studies. NO₂ is widely used in health studies as an indicator of traffic-generated air pollution in urban areas. Incorporation of high-resolution interpolated observed wind direction from a network of 38 weather stations in a LUR model improved NO₂ concentration estimates in densely populated, high traffic and industrial/business areas in Toronto-Hamilton urban airshed (THUA) of Ontario, Canada. These small-area variations in air pollution concentrations that are probably more important for health exposure studies may not be detected by sparse continuous air pollution monitoring network or conventional interpolation methods. Observed wind fields were also compared with wind fields generated by Global Environmental Multiscale-High resolution Model Application Project (GEM-HiMAP) to explore the feasibility of using regional weather forecasting model simulated wind fields in LUR models when observed data are either sparse or not available. While GEM-HiMAP predicted wind fields well at large scales, it was unable to resolve wind flow patterns at smaller scales. These results suggest caution and careful evaluation of regional weather forecasting model simulated wind fields before incorporating into human exposure models for health studies. This study has demonstrated that wind fields may be integrated into the land use regression framework. Such integration has a discernable influence on both the overall model prediction and perhaps more importantly for health effects assessment on the relative spatial distribution of traffic pollution throughout the THUA. Methodology developed in this study may be applied in other large urban areas across the world.     

Mold infestation of wet spray-applied cellulose insulation

Mold investigations were conducted in four buildings that had been insulated with wet spray-applied cellulose insulation (WSACI). Bulk WSACI samples were collected and analyzed by quantitative polymerase chain reaction (QPCR) methods. Airborne mold was evaluated using both Burkard total mold spore and Andersen culturable/viable sampling methods. Although reportedly treated with biocidal borates, QPCR analyses indicated that elevated concentrations of mold cells (reported as spore equivalents per gram) may be present in WSACI. QPCR analyses showed the following: (1) very high concentrations of Penicillium chrysogenum in samples from two of four buildings; (2) very high concentrations of Stachybotrys chartarum in samples from one building and a more moderate presence in a second; (3) moderately high concentrations of Aspergillus versicolor in samples from one building and more moderate concentrations in a second; (4) the presence of the opportunistic pathogen, Aspergillus fumigatus, in samples from three of the four buildings, and (5) the presence of 22 of 23 target mold species. Elevated airborne total mold spore concentrations were observed in all four of the buildings investigated. Culturable/viable airborne mold concentrations were moderately elevated in three of the four buildings. Mold genera/types present were relatively consistent among airborne mold samples collected by both methods and bulk sample analyses. Results of this study suggest that WSACI has the potential to cause elevated airborne mold levels in buildings where it has been applied and pose significant mold exposure and public health risks.     

Wind Tunnel Testing of Open Top Field Chambers for Plant Effects Assessment

ABSTRACT

This study reports the first field measurements of airborne exavalent chromium (Cr(vi)) in southwestern Ontario. Hexavalent chromium was identified as an inhalation carcinogen and an air toxic of concern during the 1991-93 Windsor Air Quality Study. The results of that study indicated that approximately 20% of the routinely monitored ambient airborne chromium (Cr) was in the hexavalent form. In addition, the range of carcinogenic health risks attributable to airborne Cr(vi) was determined to be between 1.4 x IO⁶ and 3.0 x 10^-4 for people living in the Windsor area. During the summer of 1993, analyses of concurrent indoor and outdoor 24-hour air quality samples taken at 33 residences in Hamilton resulted in geometric mean Cr(vi) concentrations of 0.20 r|g/m³ and 0.55 r|g/m³, respectively, and little or no relationship between the indoor and outdoor sample sets. During the summer of 1994, an airborne Cr(vi) size-fractionation study was conducted in Hamilton, the results of which suggested that the majority of the Cr(vi) was in the inhalable fraction.     

Atmospheric polycyclic aromatic hydrocarbons (PAHs) in Asia: a review from 1999 to 2004

Polycyclic aromatic hydrocarbons (PAHs) are present in both gaseous and particulate phases. These compounds are considered to be atmospheric contaminants and are human carcinogens. Many studies have monitored atmospheric particulate and gaseous phases of PAH in Asia over the past 5 years. This work compares and discusses different sample collection, pretreatment and analytical methods. The main PAH sources are traffic exhausts (AcPy, FL, Flu, PA, Pyr, CHR, BeP) and industrial emissions (BaP, BaA, PER, BeP, COR, CYC). PAH concentrations are highest in areas of traffic, followed by the urban sites, and lowest in rural sites. Meteorological conditions, such as temperature, wind speed and humidity, strongly affect PAH concentrations at all sampling sites. This work elucidates the characteristics, sources and distribution, and the healthy impacts of atmospheric PAH species in Asia.     

Compounds in Airborne Participates: Salts and Hydrocarbons

Concentrations of 10 polycyclic aromatic hydrocarbons (PAH), the aliphatlcs as a group, sulfate, nitrate, fluoride, acidity, and carbon In the airborne partlculate matter were measured at 16 sites In Cleveland, OH over a 1 year period during 1971 and 1972. Analytical methods used included gas chromatography, colorimetry, and combustion techniques. Uncertainties in the concentrations associated with the sampling procedures, and the analytical methods are evaluated. The data are discussed relative to other studies and source origins. Benzo(a)pyrene and its high concentrations downwind of coke ovens are discussed. Hydrocarbon correlation studies indicated no significant relations among compounds studied.     

Indoor- and outdoor-derived contaminants in urban and rural homes in Ottawa, Ontario, Canada

Indoor and outdoor air contaminants have largely been treated separately in studies of their respective effects on respiratory and nonrespiratory health. In this paper, we report the results of a comprehensive study of key contaminants in 10 urban and 10 rural homes in Ottawa, Ontario, Canada. The analyses included house dust mite and cat allergens along with the fungal inflammatory polysaccharide beta1,3-D-glucan in settled dust and fine particulate matter, coarse particulate matter, ergosterol, glucan, and endotoxin from air samples. In addition, black carbon was continuously measured for 7 days. A detailed physical assessment of the house and patterns of use were undertaken, including a careful inspection for mold and water damage, as well as measurements of air leakage. The performance of the houses and the range and distribution of the contaminants measured were largely similar to that of previous Canadian studies. For certain combinations, it is thought that the presence of both allergen and inflammatory materials increases asthma symptoms. House-by-house comparisons of airborne concentrations of inflammatory compounds measured (endotoxin, fine particulate matter, and fungal glucan) with dust mite allergens indicated that certain houses had relatively higher amounts of both kinds of materials.     

Analysis of Ambient Concentrations of Organic Vapors with a Passive Sampler

Volatile organic compounds can contribute to the failure of electronic equipment in both switching offices and data centers. They can also be useful indicators of ventilation needs. Only within the past decade have ambient concentrations of volatile organics been measured routinely. In standard sampling approach, a pump is used to pull a known volume of air through an adsorbent. This study examines a sampling procedure that does not use a pump, but instead depends on molecular diffusion for eventual contact between the vapor phase compounds and the charcoal sorbent (passive sampling). The technique is both simpler and less expensive than active sampling with a pump. This method has been validated for low-level sampling over extended time intervals. This study demonstrates that collected amounts vary linearly with airborne concentrations for sampling intervals in excess of four weeks: even after eight weeks of sampling at typical ambient concentrations, the amount of material collected does not approach the capacity of the sorbent. The method is applicable for concentrations spanning six orders of magnitude; reproducibility averages 13 percent of the mean value; and the sensitivity is excellent (0.06 μg/m³ or roughly 0.015 ppbv for a compound with a molecular weight of 100). The procedure has already been used successfully to monitor indoor air quality at almost a dozen telephone office and data center sites.     

Rapid Screening and Identification of Airborne Carcinogens of Greatest Concern in California

This paper describes a method for establishing a priority list of airborne carcinogens within a state Jurisdiction. In this case it was necessary to identify, from among hundreds of potential candidates, the five to ten materials of greatest potential concern in California as airborne carcinogens.

Because no previous inventory of carcinogens in California existed, published lists, rankings, and assessments of national scope were used to identify candidates. By systematic manipulation and comparison of these data sources, 47 materials of some notoriety were chosen for closer scrutiny. This selection was pared to 22 candidates largely by eliminating those which had very little production and use in California. (Substances primarily used as pesticides were excluded from the scope of this study.) The remaining candidates were then ranked by additive . and multiplicative algorithms and by a panel of experts. The results of these rankings were combined to produce a single selection of 11 priority candidates. In alphabetical order, they are arsenic, asbestos, benzene, cadmium, carbon tetrachloride, chloroform, ethylene dibromide, ethylene dichloride, N-nitrosoamines, perchloroethylene, and polycyclic aromatic hydrocarbons. In continuing studies, a baseline emissions inventory is being prepared, and a source testing program is being designed.     

Correlation between the nitrogen concentration of two epiphytic lichens and the traffic density in an urban area

A field experiment was carried out in the urban environment of the Grenoble area using two epiphytic lichens: the nitrophytic Physcia adscendens and the acidiphytic Hypogymnia physodes. Two complementary studies characterized this experiment. Firstly, a sampling of the two lichens in 48 sites randomly located throughout the Grenoble area indicated that roads (size and proximity to sampling sites) influenced the nitrogen concentrations of P. adscendens, but not those of H. physodes. Secondly, to study more accurately the influence of roads, a traffic index was calculated and applied along two transects located perpendicularly to urban motorways. Significant positive correlations were found between this traffic index and the total nitrogen concentration of P. adscendens.     

A Survey Technique for Determining The Representativeness of Urban Air Monitoring Stations With Respect to Carbon Monoxide

An air quality survey technique for measuring the horizontal spatial variation of carbon monoxide concentrations in urban areas is described; it was used to determine how representative an urban air monitoring station is of concentrations throughout the city.

The survey technique was applied in San Jose, Calif., where 1128 samples were collected over a six-month period and were compared with the values recorded simultaneously at the urban air monitoring station. All samples were collected at “breathing height” within a 13-square-mile grid which included the downtown area as well as surrounding residential and industrial locations. Three basic sampling strategies were employed to answer specific questions about the distribution of carbon monoxide concentration: (7) walking sampling, in which samples were obtained while walking along the sidewalks of congested downtown streets, (2) random spatial sampling, in which samples were collected at randomly selected points in the urban grid, and (3) specialized sampling in the immediate vicinity of the air monitoring station.

The results indicate that pedestrians on downtown streets in San Jose can be exposed to concentrations above the federal air quality standards without these values being observed at the air monitoring station. There also is evidence that, at any instant of time, similar values of carbon monoxide exist throughout this city (within a 13-square mile area), provided that measurements are not made in close proximity to streets. Furthermore, the higher concentrations observed in the immediate vicinity of streets decrease quite rapidly with increasing horizontal distance from these streets.

These findings, in the view of the authors, raise serious doubts as to whether it is possible to determine if air quality standards as currently defined are actually being met in urban areas using data from present-day air monitoring stations.     

The APCA Exhibition

On June 5 and 6 of 1980, two parallel plume oxidation studies were carried out in the vicinity of the Tennessee Valley Authority's Colbert Steam Plant. One study was performed in a smog chamber into which stack gases were injected and mixed with ambient air. The other study included direct airborne sampling of the power plant plume. Atmospheric oxidation rates for the conversion of SO₂ to SO₄ ^2- and the removal rates of NO _x (which is presumably the rate of NO₃ ^- formation) were estimated for both studies. The SO₂ to SO₄ ^2- rate coefficients were found to be 0.022 ± 0.009 h^-1 for both chamber experiments and the first airborne sampling day. For the second day, a rate constant of 0.041 ± 0.052 h^-1 was estimated from the aircraft data. The large deviation in this value is explained by the fact that the plume from the power plant combined and reacted with the urban plume from the city of Florence, AL. The formation of a very large "O3 bulge" on this day is also attributed to the mixed plumes. The first order rate coefficients for NO _x removal were estimated to be 0.27 ± 0.14 h^-1 for both chamber experiments and the first airborne sampling day. A NO _x removal rate could not be determined for the second airborne sampling day.     

Occurrence of carcinogenic amino-alpha-carbolines in some environmental samples

The carcinogenic amino-alpha-carbolines, 2-amino-9H-pyrido[2,3-b]indole and AalphaC, have been measured in airborne particles, rain water, soil and cigarette-smoke-polluted indoor air by high-performance liquid chromatography. These carcinogens were found in all kinds of environmental samples examined, although MeAalphaC was not detected in soil. Considering the present results, together with the previous findings that these carcinogens were present in foodstuffs, cigarette smoke and diesel-exhaust particles, amino-alpha-carbolines are likely to be ubiquitous environmental pollutants. Our data also support the hypothesis that amino-alpha-carbolines are formed through combustion of various materials such as food, grass and petroleum.     

Pedestrian exposure to size-resolved particles in Milan

Measurement campaigns for airborne particles along a pedestrian route in the city center of Milan were performed by means of a portable instrument consisting of an optical particle counter and a global positioning system (GPS) signal receiver. Based on the size-resolved particle number concentration data and on proper density factors experimentally determined for Milan urban area, the mass concentrations were calculated in terms of particulate matter with aerodynamic diameters < or =10 microm (PM10), < or =2.5 pm (PM2.5), and < or =1 microm (PM1). Besides directly measuring the personal exposure to PM throughout the route, the measurement campaigns pointed out small spatial and temporal variations of the concentration ranges in the different urban microenvironments visited along the route as well as very peculiar features of the particles levels in the underground subway. These findings suggested that the personal exposure of pedestrians in the city center could be estimated by simply taking into account the exposure at the open air and in the subway. The comparison between measured and calculated exposures according to the microenvironment-based estimation results in reasonable accordance, even though the estimations tend to slightly underestimate (12%) the actual measured exposure.     

Multivariate stochastic modelling of grass fluoride and airborne fluorides

Stochastic modelling was used to investigate the influence of airborne fluorides (in the case of grass fluoride) and meteorological factors on both grass and airborne fluoride levels, taking into consideration lagged dependence. Using rigorous grass sampling methods, there were indications of a negative relationship between volume of rainfall and grass fluoride concentrations, but no apparent relationship between the time which the leaf was visibly wet and grass fluoride levels. No evidence was found that rainfall washed airborne fluoride from the atmosphere or that wind variables influenced grass fluoride. For one particular experimental site, a multivariate stochastic model, which accounts for 81% of the total variation of the grass fluoride series, is developed.     

The influence of sampling protocol on nonmethane hydrocarbon mixing ratios

The effect of sampling protocol on ambient air hydrocarbon mixing ratios was examined on eight sampling days in Los Angeles during 2007 and 2008. Four protocols, which were based on previously published multi-city urban hydrocarbon studies in the United States, were compared and differences were quantified. Whole air canister samples were collected and analyzed for nonmethane hydrocarbons (NMHCs). Differing sampling protocols resulted in large differences in mixing ratios, up to an order of magnitude, for certain NMHCs on the same sampling day. However, the magnitude of the variability between NMHC levels obtained by the four protocols was not consistent throughout the eight sampling days. It was found that sampling time, followed by sampling location, had the greatest influence on the magnitude of the mixing ratio. Ratios between hydrocarbons, often used in urban studies to gain information on emission sources, also varied depending on the protocol used. Comparison of absolute NMHC mixing ratios collected in urban environments using differing sampling protocols should be made with care.     

Covariations in the concentrations of organic compounds associated with springtime atmospheric aerosols

Organic compounds that can be thermally desorbed from airborne particles change cohesively with time, providing information about sources, photochemical transformations and transport of aerosols. In the spring of 1985, 138 airborne particulate samples were collected at an urban site in Boulder, Colorado. Samples were collected by drawing approximately 300 ℓ of air, for 58 min, through a small glass tube containing a quartz fiber filter. Particles were subsequently analyzed by direct thermal desorption of volatile organic compounds into a gas Chromatographic column followed by separation and detection of compounds with flame ionization or mass spectrometry. Factor analysis on the concentrations of 42 organic compounds in 138 1-h samples with time and meteorology revealed characteristic chromatograms for photochemical activity, biological sources and motor vehicle sources. Organic compounds desorbed from particles include terpenoids from biogenic sources, alkanes from vehicular and biological sources and aldehydes, ketones, carboxylic acids, lactones and furans from photochemical transformations and other sources. Concentrations of oxygenated species increased on sunny days relative to cloudy days or nights. Terpenoid concentrations increased when the wind direction was from a forested region west of the sampling site. Odd carbon number n-alkanes increased as temperature increased with the progression of springtime.     

Indoor air quality differences between urban and rural preschools in Korea

Background, aims, and scope

Preschool indoor air quality (IAQ) is believed to be different from elementary school or higher school IAQ and preschool is the first place for social activity. Younger children are more susceptible than higher-grade children and spend more time indoors. The purpose of this study was to compare the indoor air quality by investigating the concentrations of airborne particulates and gaseous materials at preschools in urban and rural locations in Korea.

Methods

We investigated the concentrations of airborne particulates and gaseous materials in 71 classrooms at 17 Korean preschools. For comparison, outdoor air was sampled simultaneously with indoor air samples. Airborne concentrations of total suspended particulates, respirable particulates, lead, asbestos, total volatile organic compounds and components, formaldehyde, and CO₂ were measured with National Institute for Occupational Safety and Health and/or Environmental Protection Agency analytical methods.

Results

The concentration profiles of the investigated pollutants in indoor and urban settings were higher than those in outdoor and rural areas, respectively. The ratios of indoor/outdoor concentrations (I/O) of particulates and gaseous pollutants were characterized in urban and rural preschools. Total dust concentration was highest in urban indoor settings followed by urban outdoor, rural indoor, and rural outdoor locations with an I/O ratio of 1.37 in urban and 1.35 in rural areas. Although I/O ratios of lead were close to 1, lead concentrations were much higher in urban than in rural areas. The I/O ratio of total VOCs was 2.29 in urban and 2.52 in rural areas, with the highest level in urban indoor settings. The I/O ratio of formaldehyde concentrations was higher in rural than in urban areas because the outdoor rural level was much lower than the urban concentration. Since an I/O ratio higher than 1 implies the presence of indoor sources, we concluded that there are many indoor sources in preschools.

Conclusions

We confirmed that pollutants in indoor and urban settings were higher than those in outdoor and rural areas, respectively. Preschool children are expected to spend more time inside preschool facilities and therefore to be more exposed to pollutants. As far as we know, preschool IAQ is different from elementary school or higher school IAQ. Also, they are more vulnerable than higher-grade children. We found that the indoor and urban concentration profiles of the studied pollutants in preschools were higher than those in outdoor and rural areas. We believe that our findings may be useful for understanding the potential health effects of exposure and intervention studies in preschools.     

The Mass Distribution of Large Atmospheric Particles

This paper describes the results of a study to determine the total mass and the mass distribution of atmospheric aerosols, especially that mass associated with particles greater than 10 μm diameter. This study also determined what fraction of the total aerosol mass a standard high-volume air sampler collects and what fraction and size interval settle out on a dust fall plate. A special aerosol sampling system was designed for this study to obtain representative samples of large airborne particles. A suburban sampling site was selected because no local point sources of aerosols existed nearby. Samples were collected under various conditions of wind velocity and direction to obtain measurements on different types of aerosols.

Study measurements show that atmospheric particulate matter has a bimodal mass distribution. Mass associated with large particles mainly ranged from 5 to 100 μm in size, while mass associated with small particles ranged from an estimated 0.03 to 5 μm in size. Combined, these two distributions produced a bimodal mass distribution with a minimum around 5 μm diameter. The high-volume air sampler was found to collect most of the total aerosol mass, not just that fraction normally considered suspended particulate. Dust fall plates did not provide a good or very useful measure of total aerosol mass. The two fundamental processes of aerosol formation, condensation and dispersion appear to account for the formation of a bimodal mass distribution in both natural and anthropogenic aerosols. Particle size distribution measurements frequently are in error because representative samples of large airborne particles are not obtained. Considering this descrepancy, air pollution regulations should specify or be based upon an upper particle size limit.     

Particle Size Distributions of Kraft Paper Mill Aerosols Obtained by Airborne Sampling

Size distributions of particles at several downwind points in a Kraft paper mill plume have been determined by means of airborne sampling. Size distributions from samples close to the stack were found to have a log normal frequency distribution, but significant deviations from the log normal were found farther downwind. Several possible physical mechanisms are postulated as causes for this behavior. Plume dilution with background particles appears to be the most likely mechanism. The airborne sampling system is described, and electron micrographs of sampled particles are presented.