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Sample records for aerosol particulate matter

  1. PREFACE OF SPECIAL ISSUE OF AEROSOL SCIENCE AND TECHNOLOGY FOR PARTICULATE MATTER SUPERSITES PROGRAM AND RELATED STUDIES

    EPA Science Inventory

    This article is the preface or editors note to a dedicated issue of Aerosol Science and Technology, journal of the American Association for Aerosol Research. It includes a selection of scientific papers from the specialty conference entitled, "Particulate Matter Supersites ...

  2. Carbonaceous Aerosols in Fine Particulate Matter of Santiago Metropolitan Area, Chile

    PubMed Central

    Toro Araya, Richard; Flocchini, Robert; Morales Segura, Rául G. E.; Leiva Guzmán, Manuel A.

    2014-01-01

    Measurements of carbonaceous aerosols in South American cities are limited, and most existing data are of short term and limited to only a few locations. For 6 years (2002–2007), concentrations of fine particulate matter and organic and elemental carbon were measured continuously in the capital of Chile. The contribution of carbonaceous aerosols to the primary and secondary fractions was estimated at three different sampling sites and in the warm and cool seasons. The results demonstrate that there are significant differences in the levels in both the cold (March to August) and warm (September to February) seasons at all sites studied. The percent contribution of total carbonaceous aerosol fine particulate matter was greater in the cool season (53 ± 41%) than in the warm season (44 ± 18%). On average, the secondary organic carbon in the city corresponded to 29% of the total organic carbon. In cold periods, this proportion may reach an average of 38%. A comparison of the results with the air quality standards for fine particulate matter indicates that the total carbonaceous fraction alone exceeds the World Health Organization standard (10 µg/m3) and the United States Environmental Protection Agency standard (15 µg/m3) for fine particulate matter. PMID:24587753

  3. Formation of Secondary Particulate Matter by Reactions of Gas Phase Hexanal with Sulfate Aerosol Particles

    NASA Astrophysics Data System (ADS)

    Zhang, J.

    2003-12-01

    The formation of secondary particulate matter from the atmospheric oxidation of organic compounds can significantly contribute to the particulate burden, but the formation of organic secondary particulate matter is poorly understood. One way of producing organic secondary particulate matter is the oxidation of hydrocarbons with seven or more carbon atoms to get products with low vapor pressure. However, several recent reports suggest that relatively low molecular weight carbonyls can enter the particle phase by undergoing heterogeneous reactions. This may be a very important mechanism for the formation of organic secondary particulate matter. Atmospheric aldehydes are important carbonyls in the gas phase, which form via the oxidation of hydrocarbons emitted from anthropogenic and biogenic sources. In this poster, we report the results on particle growth by the heterogeneous reactions of hexanal. A 5 L Continuous Stirred Tank Reactor (CSTR) is set up to conduct the reactions in the presence of seed aerosol particles of deliquesced ammonia bisulfate. Hexanal is added into CSTR by syringe pump, meanwhile the concentrations of hexanal are monitored with High Pressure Liquid Chromatograph (HPLC 1050). A differential Mobility Analyzer (TSI 3071) set to an appropriate voltage is employed to obtain monodisperse aerosols, and another DMA associated with a Condensation Nuclear Counter (TSI 7610) is used to measure the secondary particle size distribution by the reaction in CSTR. This permits the sensitive determination of particle growth due to the heterogeneous reaction, very little growth occurs when hexanal added alone. Results for the simultaneous addition of hexanal and alcohols will also be presented.

  4. Relating hygroscopicity and composition of organic aerosol particulate matter

    SciTech Connect

    Duplissy, J.; DeCarlo, P. F.; Dommen, J.; Alfarra, M. R.; Metzger, A.; Barmpadimos, I.; Prevot, A. S. H.; Weingartner, E.; Tritscher, T.; Gysel, M.; Aiken, A. C.; Jimenez, J. L.; Canagaratna, M. R.; Worsnop, D. R.; Collins, D. R.; Tomlinson, J.; Baltensperger, U.

    2011-01-01

    A hygroscopicity tandem differential mobility analyzer (HTDMA) was used to measure the water uptake (hygroscopicity) of secondary organic aerosol (SOA) formed during the chemical and photochemical oxidation of several organic precursors in a smog chamber. Electron ionization mass spectra of the non-refractory submicron aerosol were simultaneously determined with an aerosol mass spectrometer (AMS), and correlations between the two different signals were investigated. SOA hygroscopicity was found to strongly correlate with the relative abundance of the ion signal m/z 44 expressed as a fraction of total organic signal (f44). m/z 44 is due mostly to the ion fragment CO2+ for all types of SOA systems studied, and has been previously shown to strongly correlate with organic O/C for ambient and chamber OA. The analysis was also performed on ambient OA from two field experiments at the remote site Jungfraujoch, and the megacity Mexico City, where similar results were found. A simple empirical linear relation between the hygroscopicity of OA at subsaturated RH, as given by the hygroscopic growth factor (GF) or "κorg" parameter, and f44 was determined and is given by κorg = 2.2 × f44 - 0.13. This approximation can be further verified and refined as the database for AMS and HTDMA measurements is constantly being expanded around the world. Finally, the use of this approximation could introduce an important simplification in the parameterization of hygroscopicity of OA in atmospheric models, since f44 is correlated with the photochemical age of an air mass.

  5. Biomass burning as the main source of organic aerosol particulate matter in Malaysia during haze episodes.

    PubMed

    Radzi bin Abas, M; Oros, Daniel R; Simoneit, B R T

    2004-05-01

    The haze episodes that occurred in Malaysia in September-October 1991, August-October 1994 and September-October 1997 have been attributed to suspended smoke particulate matter from biomass burning in southern Sumatra and Kalimantan, Indonesia. In the present study, polar organic compounds in aerosol particulate matter from Malaysia are converted to their trimethylsilyl derivatives and analyzed by gas chromatography-mass spectrometry in order to better assess the contribution of the biomass burning component during the haze episodes. On the basis of this analysis, levoglucosan was found to be the most abundant organic compound detected in almost all samples. The monosaccharides, alpha- and beta-mannose, the lignin breakdown products, vanillic and syringic acids and the minor steroids, cholesterol and beta-sitosterol were also present in some samples. The presence of the tracers from smoke overwhelmed the typical signatures of emissions from traffic and other anthropogenic activities in the urban areas.

  6. Concentrations and composition of aerosols and particulate matter in surface waters along the transatlantic section

    NASA Astrophysics Data System (ADS)

    Nemirovskaya, I. A.; Lisitzin, A. P.; Novigatsky, A. N.; Redzhepova, Z. U.; Dara, O. M.

    2016-07-01

    Along the transatlantic section from Ushuaia to Gdańsk (March 26-May 7, 2015; cruise 47 of R/V Akademik Ioffe), data were obtained on the concentrations of aerosols in the near-water layer of the atmosphere and of particulate matter in surface waters, as well as of organic compounds within the considered matter (Corg, chlorophyll a, lipids, and hydrocarbons). The concentrations of aerosols amounted to 1237-111 739 particles/L for the fraction of 0.3-1 μm and to 0.02-34.4 μg/m2/day for the matter collected by means of the network procedure. The distribution of aerosols is affected by circumcontinental zoning and by the fluxes from arid areas of African deserts. The maximum concentration of the treated compounds were found in the river-sea frontal area (the runoff of the Colorado River, Argentina), as well as when nearing the coasts, especially in the English Channel.

  7. DAILY VARIATION IN ORGANIC COMPOSITION OF FINE PARTICULATE MATTER IN THE DETROIT EXPOSURE AND AEROSOL RESEARCH STUDY

    EPA Science Inventory

    Organic composition of fine particulate matter (PM2.5) was investigated as a part of the Detroit Exposure and Aerosol Research Study (DEARS). A high volume (113 liters/minute) sampler was used at the Allen Park community air monitoring station to collect PM2.5 for analysis by ga...

  8. Spatial and Temporal Variability of Outdoor Coarse Particulate Matter Mass Concentrations Measured with a New Coarse Particulate Sampler during the Detroit Exposure and Aerosol Research Study

    EPA Science Inventory

    The Detroit Exposure and Aerosol Research Study (DEARS) provided data to compare outdoor residential coarse particulate matter (PM10-2.5) concentrations in six different areas of Detroit with data from a central monitoring site. Daily and seasonal influences on the spa...

  9. Study of satellite retrieved aerosol optical depth spatial resolution effect on particulate matter concentration prediction

    NASA Astrophysics Data System (ADS)

    Strandgren, J.; Mei, L.; Vountas, M.; Burrows, J. P.; Lyapustin, A.; Wang, Y.

    2014-10-01

    The Aerosol Optical Depth (AOD) spatial resolution effect is investigated for the linear correlation between satellite retrieved AOD and ground level particulate matter concentrations (PM2.5). The Multi-Angle Implementation of Atmospheric Correction (MAIAC) algorithm was developed for the Moderate Resolution Imaging Spectroradiometer (MODIS) for obtaining AOD with a high spatial resolution of 1 km and provides a good dataset for the study of the AOD spatial resolution effect on the particulate matter concentration prediction. 946 Environmental Protection Agency (EPA) ground monitoring stations across the contiguous US have been used to investigate the linear correlation between AOD and PM2.5 using AOD at different spatial resolutions (1, 3 and 10 km) and for different spatial scales (urban scale, meso-scale and continental scale). The main conclusions are: (1) for both urban, meso- and continental scale the correlation between PM2.5 and AOD increased significantly with increasing spatial resolution of the AOD, (2) the correlation between AOD and PM2.5 decreased significantly as the scale of study region increased for the eastern part of the US while vice versa for the western part of the US, (3) the correlation between PM2.5 and AOD is much more stable and better over the eastern part of the US compared to western part due to the surface characteristics and atmospheric conditions like the fine mode fraction.

  10. On-line analysis of urban particulate matter focusing on elevated wintertime aerosol concentrations.

    PubMed

    Tan, Phillip V; Evans, Greg J; Tsai, Julia; Owega, Sandy; Fila, Michael S; Malpica, Oscar; Brook, Jeffrey R

    2002-08-15

    A 10-day winter sampling campaign was conducted in downtown Toronto for particulate matter (PM) air pollution in the fine (<2.5 microm) size range. An aerosol laser ablation mass spectrometer (LAMS), a tapered-element oscillating microbalance (TEOM), and an aerodynamic particle sizer (APS) were operated in parallel to characterize the PM on-line. In this study, the LAMS observed differences in the chemical composition between three separate episodes with higher PM2.5 mass and APS counts. LAMS results showed that in one instance of elevated PM, organic amines were present in the particulates. Temporal analyses of this episode revealed chemical transformations as the amines, characterized by m/z peaks 58(C3HeN)+, 86(C5H2N)+, and nitrates, increased in number concentration while Ca and hydrocarbon particle classes concurrently decreased. On another day, sulfates were found to have increased significantly. The third event was only 4 h in duration and exhibited an increase in the number of submicron-sized K/hydrocarbons and sulfate-containing particles. In this last event, the hydrocarbons and a K to Fe ratio enrichment indicated there was likely a contribution from a combustion source. This work offers some of the first insights into single particle size and chemistry in a cold winter climate.

  11. Influence of oxygenated organic aerosols (OOAs) on the oxidative potential of diesel and biodiesel particulate matter.

    PubMed

    Stevanovic, S; Miljevic, B; Surawski, N C; Fairfull-Smith, K E; Bottle, S E; Brown, R; Ristovski, Z D

    2013-07-16

    Generally, the magnitude of pollutant emissions from diesel engines running on biodiesel fuel is ultimately coupled to the structure of the fuel's constituent molecules. Previous studies demonstrated the relationship between the organic fraction of particulate matter (PM) and its oxidative potential. Herein, emissions from a diesel engine running on different biofuels were analyzed in more detail to explore the role that different organic fractions play in the measured oxidative potential. In this work, a more detailed chemical analysis of biofuel PM was undertaken using a compact time of flight aerosol mass spectrometer (c-ToF AMS). This enabled a better identification of the different organic fractions that contribute to the overall measured oxidative potentials. The concentration of reactive oxygen species (ROS) was measured using a profluorescent nitroxide molecular probe 9-(1,1,3,3-tetramethylisoindolin-2-yloxyl-5-ethynyl)-10-(phenylethynyl)anthracene (BPEAnit). Therefore, the oxidative potential of the PM, measured through the ROS content, although proportional to the total organic content in certain cases, shows a much higher correlation with the oxygenated organic fraction as measured by the c-ToF AMS. This highlights the importance of knowing the surface chemistry of particles for assessing their health impacts. It also sheds light onto new aspects of particulate emissions that should be taken into account when establishing relevant metrics for assessing health implications of replacing diesel with alternative fuels.

  12. Comparison of different gas-phase mechanisms and aerosol modules for simulating particulate matter formation.

    PubMed

    Kim, Youngseob; Couvidat, Florian; Sartelet, Karine; Seigneur, Christian

    2011-11-01

    The effects of two gas-phase chemical kinetic mechanisms, Regional Atmospheric Chemistry Mechanism version 2 (RACM2) and Carbon-Bond 05 (CB05), and two secondary organic aerosol (SOA) modules, the Secondary Organic Aerosoi Model (SORGAM) and AER/EPRI/Caltech model (AEC), on fine (aerodynamic diameter < or =2.5 microm) particulate matter (PM2.5) formation is studied. The major sources of uncertainty in the chemistry of SOA formation are investigated. The use of all major SOA precursors and the treatment of SOA oligomerization are found to be the most important factors for SOA formation, leading to 66% and 60% more SOA, respectively. The explicit representation of high-NO, and low-NOx gas-phase chemical regimes is also important with increases in SOA of 30-120% depending on the approach used to implement the distinct SOA yields within the gas-phase chemical kinetic mechanism; further work is needed to develop gas-phase mechanisms that are fully compatible with SOA formation algorithms. The treatment of isoprene SOA as hydrophobic or hydrophilic leads to a significant difference, with more SOA being formed in the latter case. The activity coefficients may also be a major source of uncertainty, as they may differ significantly between atmospheric particles, which contain a myriad of SOA, primary organic aerosol (POA), and inorganic aerosol species, and particles formed in a smog chamber from a single precursor under dry conditions. Significant interactions exist between the uncertainties of the gas-phase chemistry and those of the SOA module.

  13. A study of aerosol properties based on observations of particulate matter from the U.S. Embassy in Beijing, China

    NASA Astrophysics Data System (ADS)

    Mukherjee, Anondo; Toohey, Darin W.

    2016-08-01

    The United States Embassy in Beijing, China publicly released a record of mass concentrations of particulate matter 2.5 µm and smaller in aerodynamic diameter (PM2.5), from April 2008 to the present, measured with a beta attenuation monitor (BAM). We compare these measurements with observations of particulate matter recorded at the Beijing Institute of Atmospheric Physics and observations of visibility recorded at the Beijing Capital International Airport (BCIA) to assess their value as a record of air quality in the greater Beijing metropolitan area. We find that the PM2.5 observations correlate well with the other observations of particulate matter (PM) over the period 1 January-1 February 2013 using a tapered element oscillating microbalance and an aerosol mass spectrometer (AMS), and they exhibit a clear inverse correlation with visibility measured at BCIA. Using inverse visibility as a proxy of radiation extinction, we determine a dry mass extinction efficiency and a dependence of radiation extinction on relative humidity, which is consistent with other studies of polluted urban environments. We deduce a strong degree of homogeneity of particulate pollution across the Beijing metropolitan region and conclude that the U.S. Embassy measurements are a reliable sample of this particulate pollution during periods of photochemical smog. The U.S. Embassy observations of PM2.5 appear to remain consistent throughout the available record and can serve as a useful dataset for studying future trends in particulate matter as China implements ambitious measures to improve air quality in the region.

  14. Use of Remotely Sensed Aerosol Optical Depth in Particulate Matter Forecasting for Urban Areas

    NASA Astrophysics Data System (ADS)

    Grant, S. L.; Crist, K.

    2011-12-01

    Cincinnati, a large metropolitan area in southwestern Ohio, has been listed as a non-attainment area based on the EPA 1997 PM2.5 (particulate matter with aerodynamic diameter < 2.5μm) standard with a number of unhealthy days reported annually for sensitive groups. AirNow provides air quality index for the city, but its accuracy largely depends on the air quality forecast models used and ground-based monitoring network measurements. These networks are inherently limited by their sparse distribution; nonetheless, they form an integral part of many decision-making structure and epidemiological studies. Remote sensing instruments such as MODIS provide daily aerosol optical depth (AOD) products with almost global spatial coverage, which are available on a near-real-time (NRT) basis. This work aims to show that the NRT AOD product obtained from MODIS can improve the air quality forecast in the Cincinnati area. To achieve this, an evaluation of the correlation of AOD retrievals with ground-based PM2.5 observations is carried out. Further to which, the MODIS AOD data is included as a variable in a statistical model to bolster current PM2.5 forecasting capabilities. Other key input parameters to the multiple linear regression model includes surface and vertical weather patterns, mixing height, local wind patterns, relative humidity and temperature.

  15. Secondary organic aerosol formation exceeds primary particulate matter emissions for light-duty gasoline vehicles

    NASA Astrophysics Data System (ADS)

    Gordon, T. D.; Presto, A. A.; May, A. A.; Nguyen, N. T.; Lipsky, E. M.; Donahue, N. M.; Gutierrez, A.; Zhang, M.; Maddox, C.; Rieger, P.; Chattopadhyay, S.; Maldonado, H.; Maricq, M. M.; Robinson, A. L.

    2013-09-01

    The effects of photochemical aging on emissions from 15 light-duty gasoline vehicles were investigated using a smog chamber to probe the critical link between the tailpipe and ambient atmosphere. The vehicles were recruited from the California in-use fleet; they represent a wide range of model years (1987 to 2011), vehicle types and emission control technologies. Each vehicle was tested on a chassis dynamometer using the unified cycle. Dilute emissions were sampled into a portable smog chamber and then photochemically aged under urban-like conditions. For every vehicle, substantial secondary organic aerosol (SOA) formation occurred during cold-start tests, with the emissions from some vehicles generating as much as 6 times the amount of SOA as primary particulate matter after three hours of oxidation inside the chamber at typical atmospheric oxidant levels. Therefore, the contribution of light duty gasoline vehicle exhaust to ambient PM levels is likely dominated by secondary PM production (SOA and nitrate). Emissions from hot-start tests formed about a factor of 3-7 less SOA than cold-start tests. Therefore, catalyst warm-up appears to be an important factor in controlling SOA precursor emissions. The mass of SOA generated by photo-oxidizing exhaust from newer (LEV1 and LEV2) vehicles was only modestly lower (38%) than that formed from exhaust emitted by older (pre-LEV) vehicles, despite much larger reductions in non-methane organic gas emissions. These data suggest that a complex and non-linear relationship exists between organic gas emissions and SOA formation, which is not surprising since SOA precursors are only one component of the exhaust. Except for the oldest (pre-LEV) vehicles, the SOA production could not be fully explained by the measured oxidation of speciated (traditional) SOA precursors. Over the time scale of these experiments, the mixture of organic vapors emitted by newer vehicles appear to be more efficient (higher yielding) in producing SOA than

  16. An Evaluation of Sharp Cut Cyclones for Sampling Diesel Particulate Matter Aerosol in the Presence of Respirable Dust

    PubMed Central

    Cauda, Emanuele; Sheehan, Maura; Gussman, Robert; Kenny, Lee; Volkwein, Jon

    2015-01-01

    Two prototype cyclones were the subjects of a comparative research campaign with a diesel particulate matter sampler (DPMS) that consists of a respirable cyclone combined with a downstream impactor. The DPMS is currently used in mining environments to separate dust from the diesel particulate matter and to avoid interferences in the analysis of integrated samples and direct-reading monitoring in occupational environments. The sampling characteristics of all three devices were compared using ammonium fluorescein, diesel, and coal dust aerosols. With solid spherical test aerosols at low particle loadings, the aerodynamic size-selection characteristics of all three devices were found to be similar, with 50% penetration efficiencies (d50) close to the design value of 0.8 µm, as required by the US Mine Safety and Health Administration for monitoring occupational exposure to diesel particulate matter in US mining operations. The prototype cyclones were shown to have ‘sharp cut’ size-selection characteristics that equaled or exceeded the sharpness of the DPMS. The penetration of diesel aerosols was optimal for all three samplers, while the results of the tests with coal dust induced the exclusion of one of the prototypes from subsequent testing. The sampling characteristics of the remaining prototype sharp cut cyclone (SCC) and the DPMS were tested with different loading of coal dust. While the characteristics of the SCC remained constant, the deposited respirable coal dust particles altered the size-selection performance of the currently used sampler. This study demonstrates that the SCC performed better overall than the DPMS. PMID:25060240

  17. Chemical speciation of vanadium in particulate matter emitted from diesel vehicles and urban atmospheric aerosols.

    PubMed

    Shafer, Martin M; Toner, Brandy M; Overdier, Joel T; Schauer, James J; Fakra, Sirine C; Hu, Shaohua; Herner, Jorn D; Ayala, Alberto

    2012-01-03

    We report on the development and application of an integrated set of analytical tools that enable accurate measurement of total, extractable, and, importantly, the oxidation state of vanadium in sub-milligram masses of environmental aerosols and solids. Through rigorous control of blanks, application of magnetic-sector-ICPMS, and miniaturization of the extraction/separation methods we have substantially improved upon published quantification limits. The study focused on the application of these methods to particulate matter (PM) emissions from diesel vehicles, both in baseline configuration without after-treatment and also equipped with advanced PM and NO(x) emission controls. Particle size-resolved vanadium speciation data were obtained from dynamometer samples containing total vanadium pools of only 0.2-2 ng and provide some of the first measurements of the oxidation state of vanadium in diesel vehicle PM emissions. The emission rates and the measured fraction of V(V) in PM from diesel engines running without exhaust after-treatment were both low (2-3 ng/mile and 13-16%, respectively). The V(IV) species was measured as the dominant vanadium species in diesel PM emissions. A significantly greater fraction of V(V) (76%) was measured in PM from the engine fitted with a prototype vanadium-based selective catalytic reductors (V-SCR) retrofit. The emission rate of V(V) determined for the V-SCR equipped vehicle (103 ng/mile) was 40-fold greater than that from the baseline vehicle. A clear contrast between the PM size-distributions of V(V) and V(IV) emissions was apparent, with the V(V) distribution characterized by a major single mode in the ultrafine (<0.25 μm) size range and the V(IV) size distribution either flat or with a small maxima in the accumulation mode (0.5-2 μm). The V(V) content of the V-SCR PM (6.6 μg/g) was 400-fold greater than that in PM from baseline (0.016 μg/g) vehicles, and among the highest of all environmental samples examined. Synchrotron

  18. Secondary organic aerosol formation exceeds primary particulate matter emissions for light-duty gasoline vehicles

    NASA Astrophysics Data System (ADS)

    Gordon, T. D.; Presto, A. A.; May, A. A.; Nguyen, N. T.; Lipsky, E. M.; Donahue, N. M.; Gutierrez, A.; Zhang, M.; Maddox, C.; Rieger, P.; Chattopadhyay, S.; Maldonado, H.; Maricq, M. M.; Robinson, A. L.

    2014-05-01

    The effects of photochemical aging on emissions from 15 light-duty gasoline vehicles were investigated using a smog chamber to probe the critical link between the tailpipe and ambient atmosphere. The vehicles were recruited from the California in-use fleet; they represent a wide range of model years (1987 to 2011), vehicle types and emission control technologies. Each vehicle was tested on a chassis dynamometer using the unified cycle. Dilute emissions were sampled into a portable smog chamber and then photochemically aged under urban-like conditions. For every vehicle, substantial secondary organic aerosol (SOA) formation occurred during cold-start tests, with the emissions from some vehicles generating as much as 6 times the amount of SOA as primary particulate matter (PM) after 3 h of oxidation inside the chamber at typical atmospheric oxidant levels (and 5 times the amount of SOA as primary PM after 5 × 106 molecules cm-3 h of OH exposure). Therefore, the contribution of light-duty gasoline vehicle exhaust to ambient PM levels is likely dominated by secondary PM production (SOA and nitrate). Emissions from hot-start tests formed about a factor of 3-7 less SOA than cold-start tests. Therefore, catalyst warm-up appears to be an important factor in controlling SOA precursor emissions. The mass of SOA generated by photooxidizing exhaust from newer (LEV2) vehicles was a factor of 3 lower than that formed from exhaust emitted by older (pre-LEV) vehicles, despite much larger reductions (a factor of 11-15) in nonmethane organic gas emissions. These data suggest that a complex and nonlinear relationship exists between organic gas emissions and SOA formation, which is not surprising since SOA precursors are only one component of the exhaust. Except for the oldest (pre-LEV) vehicles, the SOA production could not be fully explained by the measured oxidation of speciated (traditional) SOA precursors. Over the timescale of these experiments, the mixture of organic vapors

  19. Analysis of inorganic mercury species associated with airborne particulate matter/aerosols: method development.

    PubMed

    Feng, Xinbin; Lu, Julia Y; Grègoire, D Conrad; Hao, Yingjie; Banic, Catharine M; Schroeder, William H

    2004-10-01

    This paper describes a method for speciation of Hg associated with airborne particulate matter. This method uses a mini-sampler for sample collection and analysis, thermal desorption for separating Hg species, and inductively coupled plasma mass spectrometry (ICP-MS) for identification and quantification of Hg. Coal fly ash spiked with different Hg compounds (e.g. Hg0, HgCl2, HgO, and HgS) was used for qualitative calibration. A standard reference material with a certified value for Hg concentration was used to evaluate the method. When the temperature of the furnace was programmed at a linear rate of increase of 50 degrees min(-1), different Hg compounds could clearly be separated. Three airborne particulate matter samples were collected in parallel in Toronto, ON, Canada and analyzed using this method. Reproducible results were obtained and Hg0, HgCl2, HgO, and HgS species from these samples were detected.

  20. Global Estimates of Average Ground-Level Fine Particulate Matter Concentrations from Satellite-Based Aerosol Optical Depth

    NASA Technical Reports Server (NTRS)

    Van Donkelaar, A.; Martin, R. V.; Brauer, M.; Kahn, R.; Levy, R.; Verduzco, C.; Villeneuve, P.

    2010-01-01

    Exposure to airborne particles can cause acute or chronic respiratory disease and can exacerbate heart disease, some cancers, and other conditions in susceptible populations. Ground stations that monitor fine particulate matter in the air (smaller than 2.5 microns, called PM2.5) are positioned primarily to observe severe pollution events in areas of high population density; coverage is very limited, even in developed countries, and is not well designed to capture long-term, lower-level exposure that is increasingly linked to chronic health effects. In many parts of the developing world, air quality observation is absent entirely. Instruments aboard NASA Earth Observing System satellites, such as the MODerate resolution Imaging Spectroradiometer (MODIS) and the Multi-angle Imaging SpectroRadiometer (MISR), monitor aerosols from space, providing once daily and about once-weekly coverage, respectively. However, these data are only rarely used for health applications, in part because the can retrieve the amount of aerosols only summed over the entire atmospheric column, rather than focusing just on the near-surface component, in the airspace humans actually breathe. In addition, air quality monitoring often includes detailed analysis of particle chemical composition, impossible from space. In this paper, near-surface aerosol concentrations are derived globally from the total-column aerosol amounts retrieved by MODIS and MISR. Here a computer aerosol simulation is used to determine how much of the satellite-retrieved total column aerosol amount is near the surface. The five-year average (2001-2006) global near-surface aerosol concentration shows that World Health Organization Air Quality standards are exceeded over parts of central and eastern Asia for nearly half the year.

  1. Impacts of elevated-aerosol-layer and aerosol type on the correlation of AOD and particulate matter with ground-based and satellite measurements in Nanjing, southeast China.

    PubMed

    Han, Yong; Wu, Yonghua; Wang, Tijian; Zhuang, Bingliang; Li, Shu; Zhao, Kun

    2015-11-01

    Assessment of the correlation between aerosol optical depth (AOD) and particulate matter (PM) is critical to satellite remote sensing of air quality, e.g. ground PM10 and ground PM2.5. This study evaluates the impacts of aloft-aerosol-plume and aerosol-type on the correlation of AOD-PM by using synergistic measurement of a polarization-sensitive Raman-Mie lidar, CIMEL sunphotometer (SP) and TEOM PM samplers, as well as the satellite MODIS and CALIPSO, during April to July 2011 in Nanjing city (32.05(○)N/118.77(○)E), southeast China. Aloft-aerosol-layer and aerosol types (e.g. dust and non-dust or urban aerosol) are identified with the range-resolved polarization lidar and SP measurements. The results indicate that the correlations for AOD-PM10 and AOD-PM2.5 can be much improved when screening out the aloft-aerosol-layer. The linear regression slopes show significant differences for the dust and non-dust dominant aerosols in the planetary boundary layer (PBL). In addition, we evaluate the recent released MODIS-AOD product (Collection 6) from the "dark-target" (DT) and "deep-blue" (DB) algorithms and their correlation with the PM in Nanjing urban area. The results verify that the MODIS-DT AODs show a good correlation (R = 0.89) with the SP-AOD but with a systematic overestimate. In contrast, the MODIS-DB AOD shows a moderate correlation (R = 0.66) with the SP-AOD but with a smaller regression intercept (0.07). Furthermore, the moderately high correlations between the MODIS-AOD and PM10 (PM2.5) are indicated, which suggests the feasibility of PM estimate using the MODIS-AOD in Nanjing city.

  2. Opposite seasonality of the aerosol optical depth and the surface particulate matter concentration over the north China Plain

    NASA Astrophysics Data System (ADS)

    Qu, Wenjun; Wang, Jun; Zhang, Xiaoye; Sheng, Lifang; Wang, Wencai

    2016-02-01

    Great difference exists in the aerosol optical depth (AOD) between summer and winter over the North China Plain (NCP). Monthly mean AOD at 550 nm derived from the MODIS (MODerate Resolution Imaging Spectroradiometer) products during 2000-2014 over the area of 30-40° N and 110-125° E exhibits an annual maximum in June (0.855 ± 0.130) and a minimum in December (0.381 ± 0.032). This seasonality of AOD is in the opposite phase with the surface particulate matter (PM) concentration (higher in winter and lower in summer). The possible causes for the higher AOD in June (compared with December) include (a) a higher boundary layer height (BLH) that results in more efficient transport and mixing of aerosol particles to a higher altitude (corresponding to a lower particle concentration near surface) as revealed by the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations profile, (b) a higher relative humidity (RH) due to the inshore monsoon circulation that leads to enhancement of aerosol extinction, (c) emission from the regional open stalk burning in the summer harvest season (as seen from MODIS fire products), and (d) the typical eastward open topographical basin over NCP. Under the assumption that the aerosol and water vapor are well mixed within the boundary layer, analysis on multi-year average shows that the differences in BLH, RH and surface PM concentration can explain up to 81% of the variance of monthly averaged AOD over NCP. A preliminarily hypothesis is also suggested to interpret the shift of AOD pattern from winter to summer with an abrupt increase of AOD from May to June, as well as an increase of surface PM2.5 concentration over NCP during the early phase of northward progress of the East Asia summer monsoon front.

  3. A novel Aerosol-Into-Liquid Collector for online measurements of trace metal and elements in ambient particulate matter (PM)

    NASA Astrophysics Data System (ADS)

    Wang, Dongbin; Shafer, Martin; Schauer, James; Sioutas, Constantinos

    2015-04-01

    A novel monitor for online, in-situ measurement of several important metal species (i.e. Fe, Mn and Cr) in ambient fine and ultrafine particulate matter (PM) is developed based on a recent published high flow rate Aerosol-Into-Liquid Collector. This Aerosol-Into-Liquid Collector collects particles directly as highly concentrated slurry samples, and the concentrations of target metals in slurry samples are subsequently determined in a Micro Volume Flow Cell (MVFC) coupled with absorbance spectrophotometry to detect colored complexes coming from the reactions between target metals and specific reagents. Laboratory tests are conducted to evaluate the performance of the MVFC-absorbance system. The calibration curves of the system are determined using standard solutions prepared by serial dilution. As part of the evaluation, the effects of reaction time, reagent amount and interference on the system are also evaluated. Field evaluations of the online monitor will be performed to validate the ability of this new online sampler in near-continuous collection and measurements. Both laboratory and field evaluations of the novel monitor will indicate that it is an effective and valuable technology for PM collection and characterization of important metal species in ambient aerosols.

  4. INDOOR/OUTDOOR AEROSOL CONCENTRATION RATIOS DURING THE 1999 FRESNO PARTICULATE MATTER EXPOSURE STUDIES AS A FUNCTION OF SIZE, SEASON, AND TIME OF DAY

    EPA Science Inventory

    The 1999 Fresno particulate matter exposure studies tools place in February (winter season) and April/May (spring season) for two periods of four weeks. During that time, near-continuous measurements of indoor and outdoor aerosol concentrations were made with a scanning mobilit...

  5. Composition and major sources of organic compounds of aerosol particulate matter sampled during the ACE-Asia campaign

    NASA Astrophysics Data System (ADS)

    Simoneit, Bernd R. T.; Kobayashi, Minoru; Mochida, Michihiro; Kawamura, Kimitaka; Lee, Meehye; Lim, Ho-Jin; Turpin, Barbara J.; Komazaki, Yuichi

    2004-10-01

    The organic compound tracers of atmospheric particulate matter, as well as organic carbon (OC) and elemental carbon (EC), have been characterized for samples acquired during the Asian Pacific Regional Aerosol Characterization Experiment (ACE-Asia) from Gosan, Jeju Island, Korea, from Sapporo, Japan, and from Chichi-jima Island in the western North Pacific, as well as on the National Oceanic and Atmospheric Administration R/V Ronald H. Brown. Total extracts were analyzed by gas chromatography-mass spectrometry to determine both polar and aliphatic compounds. Total particles, organic matter, and lipid and saccharide compounds were high during the Asian dust episode (early April 2001) compared to levels at other times. The organic matter can be apportioned to seven emission sources and to significant oxidation-producing secondary products during long-range transport. Terrestrial natural background compounds are vascular plant wax lipids derived from direct emission and as part of desert sand dust. Fossil fuel utilization is obvious and derives from petroleum product and coal combustion emissions. Saccharides are a major polar (water-soluble) carbonaceous fraction derived from soil resuspension (agricultural activities). Biomass-burning smoke is evident in all samples and seasons. It contributes up to 13% of the total compound mass as water-soluble constituents. Burning of refuse is another source of organic particles. Varying levels of marine-derived lipids are superimposed during aerosol transport over the ocean. Secondary oxidation products increase with increasing transport distance and time. The ACE-Asia aerosols are composed not only of desert dust but also of soil dust, smoke from biomass and refuse burning, and emissions from fossil fuel use in urban areas.

  6. Characterizing particulate matter emissions from vehicles: chassis-dynamometer tests using a High-Resolution Aerosol Mass Spectrometer

    NASA Astrophysics Data System (ADS)

    Collier, S.; Zhang, Q.; Forestieri, S.; Kleeman, M.; Cappa, C. D.; Kuwayama, T.

    2012-12-01

    During September of 2011 a suite of real-time instruments was used to sample vehicle emissions at the California Air Resources Board Haagen-Schmidt facility in El Monte, CA. A representative fleet of 8 spark ignition gasoline vehicles, a diesel passenger vehicle, a gasoline direct-injection vehicle and an ultra-low emissions vehicle were tested on a chassis dynamometer. The emissions were sampled into the facility's standard CVS tunnel and diluted to atmospherically relevant levels (5-30 μg/m3) while controlling other factors such as relative humidity or background black carbon particulate loading concentrations. An Aerodyne High Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-MS) was among the real-time instruments used and sampled vehicle emissions at 10 second time resolution in order to characterize the non-refractory organic and inorganic particulate matter (PM). PM composition and concentration were tracked throughout the cold start driving cycle which included periods of fast acceleration and high velocity cruise control, meant to recreate typical commuter driving behavior. Variations in inorganic and organic PM composition for a given vehicle throughout the driving cycle as well as for various vehicles with differing emissions loading were characterized. Differences in PM composition for a given vehicle whose emissions are being exposed to differing experimental conditions such as varying relative humidity will also be reported. In conjunction with measurements from a Multi Wavelength Photoacoustic Black Carbon Spectrometer (MWPA-BC) and real-time gas measurements from the CARB facility, we determine the real-time emission ratios of primary organic aerosols (POA) with respect to BC and common combustion gas phase pollutants and compared to different vehicle driving conditions. The results of these tests offer the vehicle emissions community a first time glimpse at the real-time behavior of vehicle PM emissions for a variety of conditions and

  7. Particulate matter fugitive dusts

    SciTech Connect

    Not Available

    1988-01-01

    Topics covered in this conference include: Review of EPA's cost/benefit analysis for additional regulation of surface coal mines; Particulate monitoring on the Kilauea East Rift, Hawaii, and The MEDUSA sampling system: case histories in the measurement of particulate matter with wide spectrum analysis.

  8. Daily measurement of organic compounds in ambient particulate matter in Augsburg, Germany: new aspects on aerosol sources and aerosol related health effects.

    PubMed

    Schnelle-Kreis, Jürgen; Küpper, Ute; Sklorz, Martin; Cyrys, Josef; Briedé, Jacob Jan; Peters, Annette; Zimmermann, Ralf

    2009-07-01

    Several epidemiological studies have shown that in the human population ambient particulate matter (PM) is associated with adverse health effects. Little is known, however, about the relative effects of aerosol constituents. Since 2002, diurnal samples of ambient PM2.5 were analysed by automated methods for the quantification of particle-associated organic compounds (POC). Data on chemical composition have been investigated in epidemiological and biological effect studies. As a result of these studies, the associations found between PAH concentration and symptoms of myocardial infarction survivors suggest a major influence of combustion sources on cardiovascular health effects. The correlations found between formation of reactive oxygen species and the presence of specific organic compounds suggests an important influence of biomass combustion particles in PM2.5-associated oxidative stress.

  9. Characterization of particulate matter emissions from on-road gasoline and diesel vehicles using a soot particle aerosol mass spectrometer

    NASA Astrophysics Data System (ADS)

    Dallmann, T. R.; Onasch, T. B.; Kirchstetter, T. W.; Worton, D. R.; Fortner, E. C.; Herndon, S. C.; Wood, E. C.; Franklin, J. P.; Worsnop, D. R.; Goldstein, A. H.; Harley, R. A.

    2014-02-01

    Particulate matter (PM) emissions were measured in July 2010 from on-road motor vehicles driving through a highway tunnel in the San Francisco Bay area. A soot particle aerosol mass spectrometer (SP-AMS) was used to measure the chemical composition of PM emitted by gasoline and diesel vehicles at high time resolution. Organic aerosol (OA) and black carbon (BC) concentrations were measured during various time periods that had different levels of diesel influence, as well as directly in the exhaust plumes of individual heavy-duty (HD) diesel trucks. BC emission factor distributions for HD trucks were more skewed than OA distributions, with the highest 10% of trucks accounting for 56 and 42% of total measured BC and OA emissions, respectively. A comparison of measured OA and BC mass spectra across various sampling periods revealed a high degree of similarity in BC and OA emitted by gasoline and diesel engines. Cycloalkanes predominate in exhaust OA emissions relative to saturated alkanes (i.e., normal and iso-paraffins), suggesting that lubricating oil rather than fuel is the dominant source of primary organic aerosol (POA) emissions in diesel vehicle exhaust. This finding is supported by the detection of trace elements such as zinc and phosphorus in the exhaust plumes of individual trucks. Trace elements were emitted relative to total OA at levels that are consistent with typical weight fractions of commonly used additives present in lubricating oil. The presence of trace elements in vehicle exhaust raises the concern that ash deposits may accumulate over time in diesel particle filter systems, and may eventually lead to performance problems that require servicing.

  10. Characterization of particulate matter emissions from on-road gasoline and diesel vehicles using a soot particle aerosol mass spectrometer

    NASA Astrophysics Data System (ADS)

    Dallmann, T. R.; Onasch, T. B.; Kirchstetter, T. W.; Worton, D. R.; Fortner, E. C.; Herndon, S. C.; Wood, E. C.; Franklin, J. P.; Worsnop, D. R.; Goldstein, A. H.; Harley, R. A.

    2014-07-01

    Particulate matter (PM) emissions were measured in July 2010 from on-road motor vehicles driving through a highway tunnel in the San Francisco Bay area. A soot particle aerosol mass spectrometer (SP-AMS) was used to measure the chemical composition of PM emitted by gasoline and diesel vehicles at high time resolution. Organic aerosol (OA) and black carbon (BC) concentrations were measured during various time periods that had different levels of diesel influence, as well as directly in the exhaust plumes of individual heavy-duty (HD) diesel trucks. BC emission factor distributions for HD trucks were more skewed than OA distributions (N = 293), with the highest 10% of trucks accounting for 56 and 42% of total measured BC and OA emissions, respectively. OA mass spectra measured for HD truck exhaust plumes show cycloalkanes are predominate in exhaust OA emissions relative to saturated alkanes (i.e., normal and iso-paraffins), suggesting that lubricating oil rather than fuel is the dominant source of primary organic aerosol (POA) emissions in diesel vehicle exhaust. This finding is supported by the detection of trace elements such as zinc and phosphorus in the exhaust plumes of individual trucks. Trace elements were emitted relative to total OA at levels that are consistent with typical weight fractions of commonly used additives present in lubricating oil. A comparison of measured OA and BC mass spectra across various sampling periods revealed a high degree of similarity in OA and BC emitted by gasoline and diesel engines. This finding indicates a large fraction of OA in gasoline exhaust is lubricant-derived as well. The similarity in OA and BC mass spectra for gasoline and diesel engine exhaust is likely to confound ambient source apportionment efforts to determine contributions to air pollution from these two important sources.

  11. The Southeastern Aerosol Research and Characterization Study, Part 3: Continuous measurements of fine particulate matter mass and composition

    SciTech Connect

    Edgerton, E.S.; Hartsell, B.E.; Saylor, R.D.; Jansen, J.J.; Hansen, D.A.; Hidy, G.M.

    2006-09-15

    Deployment of continuous analyzers in the Southeastern Aerosol Research and Characterization Study (SEARCH) network began in 1998 and continues today as new technologies are developed. Measurement of fine particulate matter (PM2.5) mass is performed using a dried, 30 {sup o}C tapered element oscillating microbalance (TEOM). TEOM measurements are complemented by observations of light scattering by nephelometry. Measurements of major constituents include: (1) SO{sub 4}{sup 2-} via reduction to SO{sub 2}; (2) NH{sub 4}{sup +} and NO{sub 3}{sup -} via respective catalytic oxidation and reduction to NO, (3) black carbon (BC) by optical absorption,(4) total carbon by combustion to CO{sup 2}, and (5) organic carbon by difference between the latter two measurements. Several illustrative examples of continuous data from the SEARCH network are presented. A distinctive composite annual average diurnal pattern is observed for PM2.5 mass, nitrate, and BC, likely indicating the influence of traffic-related emissions, growth, and break up of the boundary layer and formation of ammonium nitrate. Examination of PM2.5 components indicates the need to better understand the continuous composition of the unmeasured 'other' category, because it contributes a significant fraction to total mass during periods of high PM2.5 loading. Selected episodes are presented to illustrate applications of SEARCH data. An SO{sub 2} conversion rate of 0.2%/hr is derived from an observation of a plume from a coal-fired power plant during early spring, and the importance of local, rural sources of NH{sub 3} to the formation of ammonium nitrate in particulate matter (PM) is demonstrated. 41 refs., 15 figs., 3 tabs.

  12. Fine Particulate Matter Predictions Using High Resolution Aerosol Optical Depth (AOD) Retrievals

    NASA Technical Reports Server (NTRS)

    Chudnovsky, Alexandra A.; Koutrakis, Petros; Kloog, Itai; Melly, Steven; Nordio, Francesco; Lyapustin, Alexei; Wang, Jujie; Schwartz, Joel

    2014-01-01

    To date, spatial-temporal patterns of particulate matter (PM) within urban areas have primarily been examined using models. On the other hand, satellites extend spatial coverage but their spatial resolution is too coarse. In order to address this issue, here we report on spatial variability in PM levels derived from high 1 km resolution AOD product of Multi-Angle Implementation of Atmospheric Correction (MAIAC) algorithm developed for MODIS satellite. We apply day-specific calibrations of AOD data to predict PM(sub 2.5) concentrations within the New England area of the United States. To improve the accuracy of our model, land use and meteorological variables were incorporated. We used inverse probability weighting (IPW) to account for nonrandom missingness of AOD and nested regions within days to capture spatial variation. With this approach we can control for the inherent day-to-day variability in the AOD-PM(sub 2.5) relationship, which depends on time-varying parameters such as particle optical properties, vertical and diurnal concentration profiles and ground surface reflectance among others. Out-of-sample "ten-fold" cross-validation was used to quantify the accuracy of model predictions. Our results show that the model-predicted PM(sub 2.5) mass concentrations are highly correlated with the actual observations, with out-of- sample R(sub 2) of 0.89. Furthermore, our study shows that the model captures the pollution levels along highways and many urban locations thereby extending our ability to investigate the spatial patterns of urban air quality, such as examining exposures in areas with high traffic. Our results also show high accuracy within the cities of Boston and New Haven thereby indicating that MAIAC data can be used to examine intra-urban exposure contrasts in PM(sub 2.5) levels.

  13. PREFACE: SPECIAL ISSUE OF AEROSOL SCIENCE AND TECHNOLOGY ON FINDINGS FROM THE FINE PARTICULATE MATTER SUPERSITES PROGRAM

    EPA Science Inventory

    This collection of papers, which is the first coordinated publication of results from the Phase II Supersites Program, reflects the objectives of the program - to characterize particulate matter, to provide information, such as source-receptor relationships, that support health...

  14. Impact of global climate change on ozone, particulate matter, and secondary organic aerosol concentrations in California: A model perturbation analysis

    NASA Astrophysics Data System (ADS)

    Horne, Jeremy R.; Dabdub, Donald

    2017-03-01

    Air quality simulations are performed to determine the impact of changes in future climate and emissions on regional air quality in the South Coast Air Basin (SoCAB) of California. The perturbation parameters considered in this study include (1) temperature, (2) absolute humidity, (3) biogenic VOC emissions due to temperature changes, and (4) boundary conditions. All parameters are first perturbed individually. In addition, the impact of simultaneously perturbing more than one parameter is analyzed. Air quality is simulated with meteorology representative of a summertime ozone pollution episode using both a baseline 2005 emissions inventory and a future emissions projection for the year 2023. Different locations within the modeling domain exhibit varying degrees of sensitivity to the perturbations considered. Afternoon domain wide average ozone concentrations are projected to increase by 13-18% as a result of changes in future climate and emissions. Afternoon increases at individual locations range from 10 to 36%. The change in afternoon particulate matter (PM) levels is a strong function of location in the basin, ranging from -7.1% to +4.7% when using 2005 emissions and -8.6% to +1.7% when using 2023 emissions. Afternoon secondary organic aerosol (SOA) concentrations for the entire domain are projected to decrease by over 15%, and the change in SOA levels is not a strong function of the emissions inventory utilized. Temperature increases play the dominant role in determining the overall impact on ozone, PM, and SOA concentrations in both the individual and combined perturbation scenarios.

  15. Phenols and hydroxy-PAHs (arylphenols) as tracers for coal smoke particulate matter: source tests and ambient aerosol assessments

    SciTech Connect

    Bernd R.T. Simoneit; Xinhui Bi; Daniel R. Oros; Patricia M. Medeiros; Guoying Sheng; Jiamo Fu

    2007-11-01

    Source tests were conducted to analyze and characterize diagnostic key tracers for emissions from burning of coals with various ranks. Coal samples included lignite from Germany, semibituminous coal from Arizona, USA, bituminous coal from Wales, UK and sample from briquettes of semibituminous coal, bituminous coal and anthracite from China. Ambient aerosol particulate matter was also collected in three areas of China and a background area in Corvallis, OR (U.S.) to confirm the presence of tracers specific for coal smoke. The results showed a series of aliphatic and aromatic hydrocarbons and phenolic compounds, including PAHs and hydroxy-PAHs as the major tracers, as well as a significant unresolved complex mixture (UCM) of compounds. The tracers that were found characteristic of coal combustion processes included hydroxy-PAHs and PAHs. Atmospheric ambient samples from Beijing and Taiyuan, cities where coal is burned in northern China, revealed that the hydroxy-PAH tracers were present during the wintertime, but not in cities where coal is not commonly used (e.g., Guangzhou, South China). Thus, the mass of hydroxy-PAHs can be apportioned to coal smoke and the source strength modeled by summing the proportional contents of EC (elemental carbon), PAHs, UCM and alkanes with the hydroxy-PAHs. 36 refs., 2 figs., 3 tabs.

  16. Empirical Relationship between particulate matter and Aerosol Optical Depth over Northern Tien-Shan, Central Asia

    EPA Science Inventory

    Measurements were obtained at two sites in northern Tien-Shan in Central Asia during a 1-year period beginning July 2008 to examine the statistical relationship between aerosol optical depth (AOD) and of fine [PM2.5, particles less than 2.5 μm aerodynamic diameter (AD)] and coars...

  17. Chemical characterization of fine particulate matter in Changzhou, China, and source apportionment with offline aerosol mass spectrometry

    NASA Astrophysics Data System (ADS)

    Ye, Zhaolian; Liu, Jiashu; Gu, Aijun; Feng, Feifei; Liu, Yuhai; Bi, Chenglu; Xu, Jianzhong; Li, Ling; Chen, Hui; Chen, Yanfang; Dai, Liang; Zhou, Quanfa; Ge, Xinlei

    2017-02-01

    Knowledge of aerosol chemistry in densely populated regions is critical for effective reduction of air pollution, while such studies have not been conducted in Changzhou, an important manufacturing base and populated city in the Yangtze River Delta (YRD), China. This work, for the first time, performed a thorough chemical characterization on the fine particulate matter (PM2.5) samples, collected during July 2015 to April 2016 across four seasons in this city. A suite of analytical techniques was employed to measure the organic carbon (OC), elemental carbon (EC), water-soluble organic carbon (WSOC), water-soluble inorganic ions (WSIIs), trace elements, and polycyclic aromatic hydrocarbons (PAHs) in PM2.5; in particular, an Aerodyne soot particle aerosol mass spectrometer (SP-AMS) was deployed to probe the chemical properties of water-soluble organic aerosol (WSOA). The average PM2.5 concentration was found to be 108.3 µg m-3, and all identified species were able to reconstruct ˜ 80 % of the PM2.5 mass. The WSIIs occupied about half of the PM2.5 mass (˜ 52.1 %), with SO42-, NO3-, and NH4+ as the major ions. On average, nitrate concentrations dominated over sulfate (mass ratio of 1.21), indicating that traffic emissions were more important than stationary sources. OC and EC correlated well with each other and the highest OC / EC ratio (5.16) occurred in winter, suggesting complex OC sources likely including both secondary and primary ones. Concentrations of eight trace elements (Mn, Zn, Al, B, Cr, Cu, Fe, Pb) can contribute up to ˜ 5.0 % of PM2.5 during winter. PAH concentrations were also high in winter (140.25 ng m-3), which were predominated by median/high molecular weight PAHs with five and six rings. The organic matter including both water-soluble and water-insoluble species occupied ˜ 21.5 % of the PM2.5 mass. SP-AMS determined that the WSOA had average atomic oxygen-to-carbon (O / C), hydrogen-to-carbon (H / C), nitrogen-to-carbon (N / C), and organic

  18. Global Estimates of Ambient Fine Particulate Matter Concentrations from Satellite-Based Aerosol Optical Depth: Development and Application

    PubMed Central

    van Donkelaar, Aaron; Martin, Randall V.; Brauer, Michael; Kahn, Ralph; Levy, Robert; Verduzco, Carolyn; Villeneuve, Paul J.

    2010-01-01

    Background Epidemiologic and health impact studies of fine particulate matter with diameter < 2.5 μm (PM2.5) are limited by the lack of monitoring data, especially in developing countries. Satellite observations offer valuable global information about PM2.5 concentrations. Objective In this study, we developed a technique for estimating surface PM2.5 concentrations from satellite observations. Methods We mapped global ground-level PM2.5 concentrations using total column aerosol optical depth (AOD) from the MODIS (Moderate Resolution Imaging Spectroradiometer) and MISR (Multiangle Imaging Spectroradiometer) satellite instruments and coincident aerosol vertical profiles from the GEOS-Chem global chemical transport model. Results We determined that global estimates of long-term average (1 January 2001 to 31 December 2006) PM2.5 concentrations at approximately 10 km × 10 km resolution indicate a global population-weighted geometric mean PM2.5 concentration of 20 μg/m3. The World Health Organization Air Quality PM2.5 Interim Target-1 (35 μg/m3 annual average) is exceeded over central and eastern Asia for 38% and for 50% of the population, respectively. Annual mean PM2.5 concentrations exceed 80 μg/m3 over eastern China. Our evaluation of the satellite-derived estimate with ground-based in situ measurements indicates significant spatial agreement with North American measurements (r = 0.77; slope = 1.07; n = 1057) and with noncoincident measurements elsewhere (r = 0.83; slope = 0.86; n = 244). The 1 SD of uncertainty in the satellite-derived PM2.5 is 25%, which is inferred from the AOD retrieval and from aerosol vertical profile errors and sampling. The global population-weighted mean uncertainty is 6.7 μg/m3. Conclusions Satellite-derived total-column AOD, when combined with a chemical transport model, provides estimates of global long-term average PM2.5 concentrations. PMID:20519161

  19. Study on particulate matter air pollution in Beijing with MODIS aerosol level 2 products

    NASA Astrophysics Data System (ADS)

    Mao, Jietai; Li, Chengcai; Lau, Alexis K.

    2004-09-01

    In the run-up to the 2008 Olympic Games in Beijing, Chinese government officials at both the central and municipal levels are keenly aware that they must transform Beijing into a world-class city. According to the Beijing Municipal Environmental Protection Bureau (BJEPB) to improve its air quality some actions are adopting, including taking steps to increase the forested area surrounding the city preventing dust storms, reducing the automotive vehicles, moving polluting factories now inside the fourth ring road ringing the inner city to locations outside of the fourth ring road, and switching the fuel of public buses and taxis from diesel to natural gas, etc. Will they eliminate most serious environmental problems in Beijing? MODIS aerosol products are helping us to answer this kind of questions. A long-term validation has been finished by sun-photometer observations, and the results proved the relative error of MODIS level 2 products was slightly larger than the estimation of Chu et al. (2002) from the results in most AERONET sites. However, the comparison between the products and moisture-corrected air pollution index (API) data, which were daily released to public by EPB, showed a high correlation coefficient. An air pollution episode in 2003 was investigated by the usage of satellite products. Our conclusion for the air pollution control strategy in Beijing is that only reducing the pollution sources from inner city can't fully solve the pollution problems in Beijing and the regional transports from the nearby southern provinces are contributing a lot to the pollution situation in Beijing.

  20. Rigid particulate matter sensor

    SciTech Connect

    Hall, Matthew

    2011-02-22

    A sensor to detect particulate matter. The sensor includes a first rigid tube, a second rigid tube, a detection surface electrode, and a bias surface electrode. The second rigid tube is mounted substantially parallel to the first rigid tube. The detection surface electrode is disposed on an outer surface of the first rigid tube. The detection surface electrode is disposed to face the second rigid tube. The bias surface electrode is disposed on an outer surface of the second rigid tube. The bias surface electrode is disposed to face the detection surface electrode on the first rigid tube. An air gap exists between the detection surface electrode and the bias surface electrode to allow particulate matter within an exhaust stream to flow between the detection and bias surface electrodes.

  1. Lidar measurements of airborne particulate matter

    NASA Astrophysics Data System (ADS)

    Li, Guangkun; Philbrick, C. Russell

    2003-03-01

    Raman lidar techniques have been used in remote sensing to measure the aerosol optical extinction in the lower atmosphere, as well as water vapor, temperature and ozone profiles. Knowledge of aerosol optical properties assumes special importance in the wake of studies strongly correlating airborne particulate matter with adverse health effects. Optical extinction depends upon the concentration, composition, and size distribution of the particulate matter. Optical extinction from lidar returns provide information on particle size and density. The influence of relative humidity upon the growth and size of aerosols, particularly the sulfate aerosols along the northeast US region, has been investigated using a Raman lidar during several field measurement campaigns. A particle size distribution model is being developed and verified based on the experimental results. Optical extinction measurements from lidar in the NARSTO-NE-OPS program in Philadelphia PA, during summer of 1999 and 2001, have been analyzed and compared with other measurements such as PM sampling and particle size measurements.

  2. Estimating Size-Resolved Surface Particulate Matter Concentrations Using MISR High-Resolution Size-Fractionated Aerosol Optical Depth

    NASA Astrophysics Data System (ADS)

    Franklin, M.; Kalashnikova, O. V.; Garay, M. J.

    2015-12-01

    There is significant public health interest in gaining a better understanding of the health effects associated with particulate matter (PM) of different composition and size, yet ground-based monitoring data for such PM species is extremely limited. Due to their spatial and temporal coverage, satellite observations of total column aerosol optical depth (AOD) have increasingly been used to estimate surface concentrations of PM. While techniques for using satellite observations of AOD to predict surface concentrations of PM2.5 have been established, predicting surface concentrations of different particle sizes and species is more challenging. The Multi-angle Imaging SpectroRadiometer (MISR) instrument has the unique capability of estimating both total column AOD as well as total column size fractionated (small, medium and large) AOD. Using MISR AOD and AOD size fractionated products derived from high-resolution (275 m) observations reported at a spatial scale of 4.4 km in combination with national Air Quality System (AQS) monitoring data over the 2008-2009 period, we examine the association between size-fractionated MISR AOD and surface measurements of PM at different sizes (PM2.5 and PM10) and PM2.5 species (EC, OC, SO42-, NH4+) over the greater Los Angeles area. While there was a limited sample size of speciated PM data, the strongest univariate association found was between AOD and PM2.5 SO42- (R2=0.76). Incorporating meteorological data from weather stations in the area resulted in improvements to the models associating AOD with PM2.5 and PM10 mass. We found that PM2.5 was best predicted by a spatio-temporal model of AOD that also included dew point temperature and wind speed (R2=0.61), and that PM10 was best predicted by a spatio-temporal model of large fraction AOD that also included atmospheric pressure and wind speed (R2=0.65). These flexibly specified spatio-temporal models enabled reliable predictions of surface PM2.5 and PM10 concentrations at a 4.4km

  3. Comparison of the TSI Model 8520 and Grimm Series 1.108 portable aerosol instruments used to monitor particulate matter in an iron foundry.

    PubMed

    Cheng, Yu-Hsiang

    2008-03-01

    This study uses two real-time dust monitors, the TSI Model 8520 DustTrak and Grimm Series 1.108 Aerosol Spectrometer, to determine PM(10) and PM(2.5) levels simultaneously in an iron foundry. The SA Model 241 Dichotomous Sampler was used as a reference gravimetric method for comparing the measurement results obtained by these direct-reading instruments. The response to PM levels from DustTrak is higher than that of the Aerosol Spectrometer. The DustTrak provides an overestimation PM levels, and PM levels measured by an Aerosol Spectrometer are lower than actual concentrations. Calibration factors of the DustTrak and Aerosol Spectrometer are 0.74 and 1.33, respectively, when used to measure particulate matter at an iron foundry. Based on measurement results, the DustTrak provides a lower overestimation of PM(10) levels than PM(2.5) levels; that is, the response of the DustTrak increases as particle size decreases. In addition, measurement results suggest that the Aerosol Spectrometer provides precise measurements of PM(10) and PM(2.5), and measurement accuracy compared with the reference gravimetric method can be improved through a calibration factor.

  4. Development of Particulates and Aerosols Research

    NASA Technical Reports Server (NTRS)

    DeWitt, Kenneth; Rivera, Monica

    2005-01-01

    During the past year several accomplishments were made for both the Particulate Matter Characterization and Measurement System, (PMCMS) and PAGEMS projects. The PAGEMS focus is to measure particulate emissions as a function of combustor parameters such as inlet temperature, inlet pressure and fuel air ratio. These measurements are used to evaluate combustor performance in hopes of correlating particulate emissions with engine conditions. These measurements have taken place at in-house NASA combustor facilities and off-site facilities. Ths work is unique because particulate measurements at high- pressure conditions are not commonly made. Some calibration of the PAGEMS instrumentation was done as well as minor modifications to the PAGEMS plumbing setup. These led to measurement improvements. The instrumentation and measurement process for PAGEMS was assessed and new instruments such as a thermodenuder, thermal mass flow meters and a cyclone separator were purchased to improve the PAGEMS instrumentation and measurement process. A worksheet was created to simulate varying inlet conditions to the DMA. This worksheet allows the user to assess the error in the measurements when certain conditions exist. Two technical papers were written with the PAGEMS team for the EXCAVATE field project. A paper was also reviewed for an in house publication. Also data was processed and analyzed for another field project (PAX) and will be part of a third PAGEMS paper. Accomplishments were also made with the PMCMS project. The calibration of the radial differential mobility analyzer, (RDMA) in the particle sizing system in the PMCMS was completed and provided satisfactory results. The voltages used for the RDMA depending on the particle of interest were corrected. The measurement capability of the PMCMS was increased by replacing the MetOne CPC with a TSI CPC. Lastly, assistance was provided to three college summer students with calibration of their particulate equipment and Monica Rivera

  5. Particulate matter (PM) episodes at a suburban site in Hong Kong: evolution of PM characteristics and role of photochemistry in secondary aerosol formation

    NASA Astrophysics Data System (ADS)

    Qin, Yi Ming; Jie Li, Yong; Wang, Hao; Lee, Berto Paul Yok Long; Huang, Dan Dan; Keung Chan, Chak

    2016-11-01

    Episodes with high concentrations of particulate matter (PM) across the seasons were investigated during four 1-month campaigns at a suburban site in Hong Kong. High-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) measurements revealed that both regional transport and secondary formation contributed to high PM levels during the episodes at this site. Based on distinct meteorological conditions, episodes were categorized into three types: liquid water content (LWC), solar irradiance (IR), and long-range transport (LRT). Despite the difference in meteorological conditions, all episodes were characterized by a high fraction of sulfate (45-56 %) and organics (23-34 %). However, aerosols in LWC episodes were less aged, consisting of the lowest fraction of secondary organic aerosol (SOA) and the highest fraction of small particles. Large particles mixed internally while freshly formed small particles mixed externally in LWC episodes. Aerosols in LRT episodes, by contrast, were the most aged and consisted of the highest proportion of low-volatility oxygenated organic aerosol (LVOOA) and the lowest proportion of small particles. Both small and large particles mixed externally in LRT episodes. The highest proportion of semi-volatile oxygenated organic aerosol (SVOOA) and a medium proportion of small particles were observed in IR episodes. Both small and large particles were likely externally mixed during IR episodes. Furthermore, aerosols experienced the most dramatic size increase and diurnal variation, with a time lag between SVOOA and LVOOA and a gradual increase in carbon oxidation state (OSc ≈ 2 × O : C - H : C). Five out of 10 episodes were of the IR type, further reflecting the importance of this type of episode. The evolution of aerosol components in one particular episode of the IR type, which exhibited a clear land-sea breeze pattern, was examined in detail. Sulfate and SOA due to photochemical aging

  6. Chemical Characteristics of Particulate Matter from Vehicle emission using High Resolution Time of Flight Aerosol Mass Spectrometer (HR-ToF-AMS)

    NASA Astrophysics Data System (ADS)

    Park, T.; Lee, T.; Kang, S.; Lee, J.; Kim, J.; Son, J.; Yoo, H. M.; Kim, K.; Park, G.

    2015-12-01

    Car emissions are major contributors of particulate matter (PM) in the urban environment and effects of air pollution, climate change, and human activities. By increasing of interest in research of car emission for assessment of the PM control, it became require to understand the chemical composition and characteristics of the car exhaust gases and particulate matter. To understand car emission characteristics of PM, we will study PM of car emissions for five driving modes (National Institute Environmental Research (NIER)-5, NIER-9, NIER-12, NIER-14) and three fixed speed driving modes (30km/h, 70km/h, 110km/h) using different fuel types (gasoline, diesel, and LPG) at Transportation Pollution Research Center (TPRC) of NIER in Incheon, South Korea. PM chemical composition of car emission was measured for concentrations of organics, sulfate, nitrate, ammonium, PAHs, oxidation states and size distribution using an Aerodyne High Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS) and engine exhaust particle sizer (EEPS) on real-time. In the study, organics concentration was dominated for all cases of driving modes and the concentration of organics was increased in 110km/h fixed speed mode for gasoline and diesel. The presentation will provide an overview of the chemical composition of PM in the car emissions.

  7. Polarimetric discrimination of atmospheric particulate matter

    NASA Astrophysics Data System (ADS)

    Raman, Prashant; Fuller, Kirk; Gregory, Don

    2012-06-01

    A polarimeter capable of measuring the complete Mueller matrix of highly scattering samples in transmission and reflection from 300 to 1100 nm has been constructed and tested. Exploratory research has been conducted which may lead to the standoff detection of bio-aerosols in the atmosphere. The polarization properties of bsubtilis (surrogate for anthrax spore) have been compared to ambient particulate matter species such as pollen, dust and soot (all sampled onto microscope slides) and differentiating features have been identified. The application of this technique for the discrimination of bio-aerosol from background clutter has been demonstrated.

  8. Apparatus for particulate matter analysis

    DOEpatents

    Gundel, Lara A.; Apte, Michael G.; Hansen, Anthony D.; Black, Douglas R.

    2007-01-30

    The apparatus described herein is a miniaturized system for particle exposure assessment (MSPEA) for the quantitative measurement and qualitative identification of particulate content in gases. The present invention utilizes a quartz crystal microbalance (QCM) or other mass-sensitive temperature compensated acoustic wave resonator for mass measurement. Detectors and probes and light sources are used in combination for the qualitative determination of particulate matter.

  9. Application of Remotely-sensed Aerosol Optical Depth in Characterization and Forecasting of Urban Fine Particulate Matter

    NASA Astrophysics Data System (ADS)

    Grant, Shanique L.

    Emissions from local industries, particularly coal-fired power plants, have been shown to enhance the ambient pollutant budget in the Ohio River Valley (ORV) region. One pollutant that is of interest is PM2.5 due to its established link to respiratory illnesses, cardiopulmonary diseases and mortality. State and local agencies monitor the impact of the local point sources on the ambient concentrations at specific sites; however, the monitors do not provide satisfactory spatial coverage. An important metric for describing ambient particulate pollution is aerosol optical depth (AOD). It is a dimensionless geo-physical product measured remotely using satellites or ground-based light detection ranging instruments. This study focused on assessing the effectiveness of using satellite aerosol optical depth (AOD) as an indicator for PM2.5 in the ORV and two cities in Ohio. Three models, multi-linear regression (MLR), principal component analysis (PCA) -- MLR and neural network, were trained using 40% of the total dataset. The outcome was later tested to minimize error and further validated with another 40% of the dataset not included in the model development phase. Furthermore, to limit the effect of seasonality, four models representing each season were created for each city using meteorological variables known to influence PM2.5 and AOD concentration. GIS spatial analysis tool was employed to visualize and make spatial and temporal comparisons for the ORV region. Comparable spatial distributions were observed. Regression analysis showed that the highest and lowest correlations were in the summer and winter, respectively. Seasonal decomposition methods were used to evaluate trends at local Ohio monitoring stations to identify areas most suitable for improved air quality management. Over the six years of study, Cuyahoga County maintained PM2.5 concentrations above the national standard and in Hamilton County (Cincinnati) PM2.5 levels ranked above the national level for more

  10. Feasibility of the detection of trace elements in particulate matter using online High-Resolution Aerosol Mass Spectrometry

    SciTech Connect

    Salcedo, D.; Laskin, Alexander; Shutthanandan, V.; Jimenez, Jose L.

    2012-08-10

    The feasibility of using an online thermal-desorption electron-ionization high-resolution aerosol mass spectrometer (AMS) for the detection of particulate trace elements was investigated analyzing data from Mexico City obtained during the MILAGRO 2006 field campaign, where relatively high concentrations of trace elements have been reported. This potential application is of interest due to the real-time data provided by the AMS, its high sensitivity and time resolution, and the widespread availability and use of this instrument. High resolution mass spectral analysis, isotopic ratios, and ratios of different ions containing the same elements are used to constrain the chemical identity of the measured ions. The detection of Cu, Zn, As, Se, Sn, and Sb is reported. There was no convincing evidence for the detection of other trace elements commonly reported in PM. The elements detected tend to be those with lower melting and boiling points, as expected given the use of a vaporizer at 600oC in this instrument. Operation of the AMS vaporizer at higher temperatures is likely to improve trace element detection. The detection limit is estimated at approximately 0.3 ng m-3 for 5-min of data averaging. Concentration time series obtained from the AMS data were compared to concentration records determined from offline analysis of particle samples from the same times and locations by ICP (PM2.5) and PIXE (PM1.1 and PM0.3). The degree of correlation and agreement between the three instruments (AMS, ICP, and PIXE) varied depending on the element. The AMS shows promise for real-time detection of some trace elements, although additional work including laboratory calibrations with different chemical forms of these elements are needed to further develop this technique and to understand the differences with the ambient data from the other techniques. The trace elements peaked in the morning as expected for primary sources, and the many detected plumes suggest the presence of multiple

  11. Spatial and Temporal Variation in Fine Particulate Matter Mass and Chemical Composition: The Middle East Consortium for Aerosol Research Study

    PubMed Central

    Abdeen, Ziad; Heo, Jongbae; Wu, Bo; Shpund, Jacob; Vanger, Arye; Sharf, Geula; Moise, Tamar; Brenner, Shmuel; Nassar, Khaled; Saleh, Rami; Al-Mahasneh, Qusai M.; Sarnat, Jeremy A.; Schauer, James J.

    2014-01-01

    Ambient fine particulate matter (PM2.5) samples were collected from January to December 2007 to investigate the sources and chemical speciation in Palestine, Jordan, and Israel. The 24-h PM2.5 samples were collected on 6-day intervals at eleven urban and rural sites simultaneously. Major chemical components including metals, ions, and organic and elemental carbon were analyzed. The mass concentrations of PM2.5 across the 11 sites varied from 20.6 to 40.3 μg/m3, with an average of 28.7 μg/m3. Seasonal variation of PM2.5 concentrations was substantial, with higher average concentrations (37.3 μg/m3) in the summer (April–June) months compared to winter (October–December) months (26.0 μg/m3) due mainly to high contributions of sulfate and crustal components. PM2.5 concentrations in the spring were greatly impacted by regional dust storms. Carbonaceous mass was the most abundant component, contributing 40% to the total PM2.5 mass averaged across the eleven sites. Crustal components averaged 19.1% of the PM2.5 mass and sulfate, ammonium, and nitrate accounted for 16.2%, 6.4%, and 3.7%, respectively, of the total PM2.5 mass. The results of this study demonstrate the need to better protect the health and welfare of the residents on both sides of the Jordan River in the Middle East. PMID:25045751

  12. Concentrations and changes of chemical elements in aerosol particulate matter as indicators of air quality in Riyadh City, Saudi Arabia

    NASA Astrophysics Data System (ADS)

    Rushdi, A. I.; Al-Mutlaq, K. F.; Simoneit, B. R.

    2010-12-01

    : Samples of air particulate matter (PM) were collected for the determination of chemical elements from June 2006 to May 2007. PM samples were taken in two size modes (PM2.5 and PM10) using MiniVolume air samplers on rooftops of various buildings (15-25 m above ground) in the city of Riyadh. The samples were subjected to XRF analysis to determine both major (Na, Mg, Al, K, Ca, Si, P, S and Fe) and trace elements (Mn, Ni, Cu, Zn, and Ba). The results show that the concentrations of both were higher in PM10 compared to PM2.5 indicating that the major source of the atmospheric PM was local dust. Furthermore, the spatial distribution of high concentrations of PM was in the south and southeast of the city and the lowest was found in the center and north eastern part of the city. This spatial PM distribution was attributed different factors such as wind direction and velocity, existence of cement factories in the southeast of the city, the presence of buildings and trees, and paved streets in the city center that reduce the amount of dust resuspended into the atmosphere. The air quality of the city was found to range from moderate to highly unhealthy for PM2.5 and from good to highly unhealthy for PM10. The enrichment factors for the measured elements were examined and revealed two groups based on their regional distribution. The first group showed no significant spatial changes indicating it has a common source throughout the sampling grid. The second group (mainly S and Ni) showed significant changes as expected from anthropogenic inputs. The S is possibly a combination of a mineralogical (CaSO4) and fossil fuel combustion origin. The source of Ni is probably in emissions from fossil fuel combustion.

  13. Spatial and temporal variation in fine particulate matter mass and chemical composition: the Middle East Consortium for Aerosol Research Study.

    PubMed

    Abdeen, Ziad; Qasrawi, Radwan; Heo, Jongbae; Wu, Bo; Shpund, Jacob; Vanger, Arye; Sharf, Geula; Moise, Tamar; Brenner, Shmuel; Nassar, Khaled; Saleh, Rami; Al-Mahasneh, Qusai M; Sarnat, Jeremy A; Schauer, James J

    2014-01-01

    Ambient fine particulate matter (PM2.5) samples were collected from January to December 2007 to investigate the sources and chemical speciation in Palestine, Jordan, and Israel. The 24-h PM2.5 samples were collected on 6-day intervals at eleven urban and rural sites simultaneously. Major chemical components including metals, ions, and organic and elemental carbon were analyzed. The mass concentrations of PM2.5 across the 11 sites varied from 20.6 to 40.3 μg/m(3), with an average of 28.7 μg/m(3). Seasonal variation of PM2.5 concentrations was substantial, with higher average concentrations (37.3 μg/m(3)) in the summer (April-June) months compared to winter (October-December) months (26.0 μg/m(3)) due mainly to high contributions of sulfate and crustal components. PM2.5 concentrations in the spring were greatly impacted by regional dust storms. Carbonaceous mass was the most abundant component, contributing 40% to the total PM2.5 mass averaged across the eleven sites. Crustal components averaged 19.1% of the PM2.5 mass and sulfate, ammonium, and nitrate accounted for 16.2%, 6.4%, and 3.7%, respectively, of the total PM2.5 mass. The results of this study demonstrate the need to better protect the health and welfare of the residents on both sides of the Jordan River in the Middle East.

  14. Biomass burning as an important source of reactive oxygen species associated with the atmospheric aerosols in Southeastern United States - Implications for health effects of ambient particulate matter

    NASA Astrophysics Data System (ADS)

    Verma, V.; Weber, R. J. J.; Fang, T.; Xu, L.; Ng, N. L.; Russell, A. G.

    2014-12-01

    We assessed the potential of water-soluble fraction of atmospheric fine aerosols in the southeastern US to generate reactive oxygen species (ROS). ROS-generation potential of particles was quantified by the dithiothreitol (DTT) assay and involved analysis of fine particulate matter (PM) extracted from high-volume quartz filters (23 h integrated daily samples) collected for one year at various sites in different environmental settings in the southeast, including three urban Atlanta sites, and one rural site in Yorkville. Water-soluble PM extracts were further separated into the hydrophobic and hydrophilic fractions using a C-18 column, and both fractions were analyzed for the DTT activity. Organic aerosol (OA) composition was measured at selected sites using a High-Resolution Time-of-Flight Aerosol Mass Spectrophotometer (HR-ToF-AMS). The various factors of the organic aerosols, i.e. Isoprene OA (Isop-OA), hydrocarbon-like OA (HOA), less-oxidized oxygenated OA, (LO-OOA), more-oxidized OOA (MO-OOA), cooking OA (COA), and biomass burning OA (BBOA) were also resolved, and their ability to generate ROS investigated by linear regression techniques. Among all OA factors, BBOA was most consistently associated with ROS, with the highest intrinsic DTT activity of 151±20 pmol/min/μg. The water-soluble bioavailable fraction of BBOA-DTT activity is 2-3 times higher than the reported total-DTT activity of diesel exhaust particles. The total contribution of various aerosol sources to the ROS generating potential was also determined by the positive matrix factorization approach. Interestingly, biomass burning appears as the strongest source of ROS generation, with its annual contribution of 35 % to DTT activity; the contribution was higher in winter (47 %), than summer (24 %) and fall (17 %) seasons. The good agreement between the hydrophobic DTT activity with that estimated from the summed OA components, indicates that humic-like substances (HULIS), which are abundantly emitted

  15. Particulate matter and preterm birth

    EPA Science Inventory

    Particulate matter (PM) has been variably associated with preterm birth (PTB) (gestation <37 weeks), but the role played by specific chemical components of PM has been little studied. We examined the association between ambient PM <2.5 micrometers in aerodynamic diameter (PM2.S) ...

  16. Source Testing for Particulate Matter.

    ERIC Educational Resources Information Center

    DeVorkin, Howard

    Developed for presentation at the 12th Conference on Methods in Air Pollution and Industrial Hygiene Studies, University of Southern California, April, 1971, this outline covers procedures for the testing of particulate matter. These are: (1) basic requirements, (2) information required, (3) collection of samples, (4) processing of samples, (5)…

  17. Study of primary biological aerosols to characterize their diversity in particulate matter over the Indian tropical region: assessment for climatic and health impact

    NASA Astrophysics Data System (ADS)

    Priyamvada R, H.; Muthalagu, A.; R, R.; Verma, R. S.; Philip, L.; Desprès, V.; Poeschl, U.; Gunthe, S. S.

    2015-12-01

    Primary Biological Aerosol Particles (PBAPs) are ubiquitous in the Earth's atmosphere and can influence the biosphere, climate, and public health (Després et al., 2012).To study the importance of the PBAPs, it is important to have an understanding about their origin, seasonal abundance and diversity. The study of PBAPs over the Indian tropical region becomes important as it hosts ~ 18% of the world population and has a distinct climate with a systematic and cyclic monsoon season which is different from the continental climates in Europe and America. In this study, the PBAPs were characterized by the application of molecular genetic techniques involving DNA extraction, PCR amplifications, cloning and DNA sequencing. In addition, characterization of the fungal source emissions was performed to better understand the diversity, abundance, and relative contribution of the fungal aerosols. For the present study, DNA analysis was performed on a one-year air filter set of PM10 (particulate matter ≤10 mm) covering three distinct meteorological seasons, i.e. summer, monsoon, and winter. The results from DNA analysis revealed the presence of bacteria and fungi in the filter samples. The fungal source characterization performed by the DNA analysis revealed the ratio of Basidiomycota to Ascomycota to be 96:4, which is consistent with previously reported studies from airborne fungal communities in the European continental boundary layer air (Fröhlich-Nowoisky et al., 2009). In the study region, the highest species richness was found to be present in the family Agaricaceae (25.3%) followed by Polyporaceae (15.3%) and Marasmiaceae (10.81%). Agaricaceae, Polyporaceae and Psathyrellaceae were dominant families in the study region and the families like Clavariaceae, Nectriaceae, Phanerochaetachae, Pleurotaceae and Strophariaceae were found to be rare. The results will next be compared with the diversity and types of the fungi found in ambient PM10. More details will be presented.

  18. Development of a Numerical System to Improve Particulate Matter Forecasts in South Korea Using Geostationary Satellite-retrieved Aerosol Optical Data over Northeast Asia

    NASA Astrophysics Data System (ADS)

    Lee, S.; Song, C. H.; Park, R.; Park, M. E.; Han, K. M.; Kim, J.; Choi, M.; Ghim, Y. S.; Woo, J. H.

    2014-12-01

    To improve short-term particulate matter (PM) forecasts in South Korea, the initial distribution of PM composition, particularly over the upwind regions, is primarily important. To prepare the initial PM composition, the aerosol optical depth (AOD) data retrieved from a geostationary equatorial orbit (GEO) satellite sensor, GOCI (Geostationary Ocean Color Imager) which covers Northeast Asia (113°E-146°E; 25°N-47°N), were used. A spatio-temporal (ST) kriging method was used to better prepare the initial AOD distributions that were converted into the PM composition over Northeast Asia. One of the largest advantages to using the ST-kriging method in this study is that more observed AOD data can be used to prepare the best initial AOD fields. It is demonstrated in this study that the short-term PM forecast system developed with the application of the ST-kriging method can greatly improve PM10 predictions in Seoul Metropolitan Area (SMA), when evaluated with ground-based observations. For example, errors and biases of PM10 predictions decreased by ~60% and ~70%, respectively, during the first 6 h of short-term PM forecasting, compared with those without the initial PM composition. In addition, The influences of several factors (such as choices of observation operators and control variables) on the performances of the short-term PM forecast were also explored in this study.

  19. Nighttime aqueous-phase secondary organic aerosols in Los Angeles and its implication for fine particulate matter composition and oxidative potential

    NASA Astrophysics Data System (ADS)

    Saffari, Arian; Hasheminassab, Sina; Shafer, Martin M.; Schauer, James J.; Chatila, Talal A.; Sioutas, Constantinos

    2016-05-01

    Recent investigations suggest that aqueous phase oxidation of hydrophilic organic compounds can be a significant source of secondary organic aerosols (SOA) in the atmosphere. Here we investigate the possibility of nighttime aqueous phase formation of SOA in Los Angeles during winter, through examination of trends in fine particulate matter (PM2.5) carbonaceous content during two contrasting seasons. Distinctive winter and summer trends were observed for the diurnal variation of organic carbon (OC) and secondary organic carbon (SOC), with elevated levels during the nighttime in winter, suggesting an enhanced formation of SOA during that period. The nighttime ratio of SOC to OC was positively associated with the relative humidity (RH) at high RH levels (above 70%), which is when the liquid water content of the ambient aerosol would be high and could facilitate dissolution of hydrophilic primary organic compounds into the aqueous phase. Time-integrated collection and analysis of wintertime particles at three time periods of the day (morning, 6:00 a.m.-9:00 a.m.; afternoon, 11:00 a.m.-3:00 p.m.; night, 8:00 p.m.-4:00 a.m.) revealed higher levels of water soluble organic carbon (WSOC) and organic acids during the night and afternoon periods compared to the morning period, indicating that the SOA formation in winter continues throughout the nighttime. Furthermore, diurnal trends in concentrations of semi-volatile organic compounds (SVOCs) from primary emissions showed that partitioning of SVOCs from the gas to the particle phase due to the decreased nighttime temperatures cannot explain the substantial OC and SOC increase at night. The oxidative potential of the collected particles (quantified using a biological macrophage-based reactive oxygen species assay, in addition to the dithiothreitol assay) was comparable during afternoon and nighttime periods, but higher (by at least ∼30%) compared to the morning period, suggesting that SOA formation processes possibly

  20. The short-term association of selected components of fine particulate matter and mortality in the Denver Aerosol Sources and Health (DASH) study

    EPA Science Inventory

    Associations of short-term exposure to fine particulate matter (PM2.5) with daily mortality may be due to specific PM2.5 chemical components. Objectives: Daily concentrations of PM2.5 chemical species were measured over five consecutive years in Denver, CO to investigate whethe...

  1. Method of dispersing particulate aerosol tracer

    DOEpatents

    O'Holleran, Thomas P.

    1988-01-01

    A particulate aerosol tracer which comprises a particulate carrier of sheet silicate composition having a particle size up to one micron, and a cationic dopant chemically absorbed in solid solution in the carrier. The carrier is preferably selected from the group consisting of natural mineral clays such as bentonite, and the dopant is selected from the group consisting of rare earth elements and transition elements. The tracers are dispersed by forming an aqueous salt solution with the dopant present as cations, dispersing the carriers in the solution, and then atomizing the solution under heat sufficient to superheat the solution droplets at a level sufficient to prevent reagglomeration of the carrier particles.

  2. Estimating Landscape Fire Particulate Matter (PM) Emissions over Southern Africa using MSG-SEVIRI Fire Radiative Power (FRP) and MODIS Aerosol Optical Thickness Observations

    NASA Astrophysics Data System (ADS)

    Mota, Bernardo; Wooster, Martin J.

    2016-04-01

    The approach to estimating landscape fire fuel consumption based on the remotely sensed fire radiative power (FRP) thermal energy release rate, as opposed to burned area, is now relatively widely used in studies of fire emissions, including operationally within the Copernicus Atmosphere Monitoring Service (CAMS). Nevertheless, there are still limitations to the approach, including uncertainties associated with using only the few daily overpasses typically provided by polar orbiting satellite systems, the conversion between FRP and smoke emissions, and the increased likelihood that the more frequent data from geostationary systems fails to detect the (probably highly numerous) smaller (i.e. low FRP) component of a regions fire regime. In this study, we address these limitations to directly estimate fire emissions of Particular Matter (PM; or smoke aerosols) by presenting an approach combining the "bottom-up" FRP observations available every 15 minutes across Africa from the Meteosat Spinning Enhanced Visible and Infrared Imager (SEVIRI) Fire Radiative Product (FRP) processed at the EUMETSAT LSA SAF, and the "top-down" aerosol optical thickness (AOT) measures of the fire plumes themselves as measured by the Moderate-resolution Imaging Spectro-radiometer (MODIS) sensors aboard the Terra (MOD04_L2) and Aqua (MYD04_L2) satellites. We determine PM emission coefficients that relate directly to FRP measures by combining these two datasets, and the use of the almost continuous geostationary FRP observations allows us to do this without recourse to (uncertain) data on wind speed at the (unknown) height of the matching plume. We also develop compensation factors to address the detection limitations of small/low intensity (low FRP) fires, and remove the need to estimate fuel consumption by going directly from FRP to PM emissions. We derive the smoke PM emissions coefficients per land cover class by comparing the total fire radiative energy (FRE) released from individual fires

  3. Using Satellite Aerosol Retrievals to Monitor Surface Particulate Air Quality

    NASA Technical Reports Server (NTRS)

    Levy, Robert C.; Remer, Lorraine A.; Kahn, Ralph A.; Chu, D. Allen; Mattoo, Shana; Holben, Brent N.; Schafer, Joel S.

    2011-01-01

    The MODIS and MISR aerosol products were designed nearly two decades ago for the purpose of climate applications. Since launch of Terra in 1999, these two sensors have provided global, quantitative information about column-integrated aerosol properties, including aerosol optical depth (AOD) and relative aerosol type parameters (such as Angstrom exponent). Although primarily designed for climate, the air quality (AQ) community quickly recognized that passive satellite products could be used for particulate air quality monitoring and forecasting. However, AOD and particulate matter (PM) concentrations have different units, and represent aerosol conditions in different layers of the atmosphere. Also, due to low visible contrast over brighter surface conditions, satellite-derived aerosol retrievals tend to have larger uncertainty in urban or populated regions. Nonetheless, the AQ community has made significant progress in relating column-integrated AOD at ambient relative humidity (RH) to surface PM concentrations at dried RH. Knowledge of aerosol optical and microphysical properties, ambient meteorological conditions, and especially vertical profile, are critical for physically relating AOD and PM. To make urban-scale maps of PM, we also must account for spatial variability. Since surface PM may vary on a finer spatial scale than the resolution of standard MODIS (10 km) and MISR (17km) products, we test higher-resolution versions of MODIS (3km) and MISR (1km research mode) retrievals. The recent (July 2011) DISCOVER-AQ campaign in the mid-Atlantic offers a comprehensive network of sun photometers (DRAGON) and other data that we use for validating the higher resolution satellite data. In the future, we expect that the wealth of aircraft and ground-based measurements, collected during DISCOVER-AQ, will help us quantitatively link remote sensed and ground-based measurements in the urban region.

  4. Advanced particulate matter control apparatus and methods

    DOEpatents

    Miller, Stanley J [Grand Forks, ND; Zhuang, Ye [Grand Forks, ND; Almlie, Jay C [East Grand Forks, MN

    2012-01-10

    Apparatus and methods for collection and removal of particulate matter, including fine particulate matter, from a gas stream, comprising a unique combination of high collection efficiency and ultralow pressure drop across the filter. The apparatus and method utilize simultaneous electrostatic precipitation and membrane filtration of a particular pore size, wherein electrostatic collection and filtration occur on the same surface.

  5. PARTICULATE MATTER, OXIDATIVE STRESS AND ...

    EPA Pesticide Factsheets

    Particulate matter (PM), a component of air pollution has been epidemiologically associated with sudden deaths, cardiovascular and respiratory illnesses. The effects are more pronounced in patients with pre-existing conditions such as asthma, diabetes or obstructive pulmonary disorders. Clinical and experimental studies have historically focused on the cardiopulmonary effects of PM. However, since PM particles carry numerous biocontaminants that are capable of triggering free radical production and cytokine release, the possibility that PM may affect organs systems sensitive to oxidative stress must be considered. Four independent studies that summarize the neurochemical and neuropathological changes found in the brains of PM exposed animals are described here. These were recently presented at two 2007 symposia sponsored by the Society of Toxicology (Charlotte, NC) and the International Neurotoxicology Association (Monterey, CA). Particulates are covered with biocontaminants (e.g., endotoxins, mold, pollen) which convey free radical activity that can damage the lipids, nucleic acids, and proteins of target cells on contact and stimulate inflammatory cytokine release. Although, the historical focus of PM toxicity has been cardiopulmonary targets, it is now appreciated that inhaled nano-size (<100 nm) particles quickly exit the lungs and enter the circulation where they distribute to various organ systems (l.e., liver, kidneys, testes, lymph nodes) (Takenaka et aI

  6. Composition and oxidation state of sulfur in atmospheric particulate matter

    NASA Astrophysics Data System (ADS)

    Longo, Amelia F.; Vine, David J.; King, Laura E.; Oakes, Michelle; Weber, Rodney J.; Huey, Lewis Gregory; Russell, Armistead G.; Ingall, Ellery D.

    2016-10-01

    The chemical and physical speciation of atmospheric sulfur was investigated in ambient aerosol samples using a combination of sulfur near-edge x-ray fluorescence spectroscopy (S-NEXFS) and X-ray fluorescence (XRF) microscopy. These techniques were used to determine the composition and oxidation state of sulfur in common primary emission sources and ambient particulate matter collected from the greater Atlanta area. Ambient particulate matter samples contained two oxidation states: S0 and S+VI. Ninety-five percent of the individual aerosol particles (> 1 µm) analyzed contain S0. Linear combination fitting revealed that S+VI in ambient aerosol was dominated by ammonium sulfate as well as metal sulfates. The finding of metal sulfates provides further evidence for acidic reactions that solubilize metals, such as iron, during atmospheric transport. Emission sources, including biomass burning, coal fly ash, gasoline, diesel, volcanic ash, and aerosolized Atlanta soil, and the commercially available bacterium Bacillus subtilis, contained only S+VI. A commercially available Azotobacter vinelandii sample contained approximately equal proportions of S0 and S+VI. S0 in individual aerosol particles most likely originates from primary emission sources, such as aerosolized bacteria or incomplete combustion.

  7. Speciation of The Particulate Organic Matter In Three Remote Areas

    NASA Astrophysics Data System (ADS)

    Masclet, Pierre; Marchand, Nicolas; Jaffrezo, Jean Luc; Besombes, Jean Luc

    Total particulate matter was collected as part of three programs between 1999 and 2001 (EAAS in Finland, ESOMPTE in Marseille/Fos and POVA in french alpine valleys). The speciation of the particulate organic matter (POM) was performed by Gas Chromatography or HPLC coupled with a mass spectrometer. 13 organic families were identified in the 245 samples collected. The presence of some functional groups (- COOH; - OH and - CHO) and the carbon chain length are used in order to identify the sources of the particulate pollutants and the physicochemical behaviour during the long range atmospheric transport of the aerosol. The composition of the POM differs depending on the season (the secondary fraction reaches 27 % in summer and only 6% in winter) and on the remoteness of the sources. Alkanes are always the most abundant compounds. Polycyclic aromatic hydrocarbons, alcohols, esters, carboxylic acids and monoaromatic hydrocarbons are present in significant abundance. Some alkenes, aldehydes, ether oxydes, ketones and halocompounds are also found. Alcohols are more abundant in aerosols collected close to marine sites. Long carbon chain esters are mostly found in aerosols collected in high density vegetation areas and relatively high concentrations of PAH are measured in aerosols collected close to highly populated areas. These three families are good geochemical tracers, respectively of marine, biogenic and anthropic sources.

  8. PARTICULATE MATTER, OXIDATIVE STRESS AND NEUROTOXICITY

    EPA Science Inventory

    Particulate matter (PM), a component of air pollution has been epidemiologically associated with sudden deaths, cardiovascular and respiratory illnesses. The effects are more pronounced in patients with pre-existing conditions such as asthma, diabetes or obstructive pulmonary dis...

  9. Particulate matter, oxidative stress and neurotoxicity.

    EPA Science Inventory

    Particulate matter (PM), a component of air pollution has been epidemiologically associated with sudden deaths, cardiovascular and respiratory illnesses. The effects are more pronounced in patients with pre-existing conditions such as asthma, diabetes or obstructive pulmonary dis...

  10. OPEN PATH OPTICAL SENSING OF PARTICULATE MATTER

    EPA Science Inventory

    The paper discusses the concepts behind recent developments in optical remote sensing (ORS) and the results from experiments. Airborne fugitive and fine particulate matter (PM) from various sources contribute to exceedances of state and federal PM and visibility standards. Recent...

  11. Particulate Matter (Environmental Health Student Portal)

    MedlinePlus

    ... Pollutants Natural Disasters Drinking Water Waterborne Diseases & Illnesses Water Cycle Water Treatment Videos Games Experiments For Teachers Home ... Pollutants Natural Disasters Drinking Water Waterborne Diseases & Illnesses Water Cycle Water Treatment Particulate Matter The Basics We’ve ...

  12. Methods of analysis for complex organic aerosol mixtures from urban emission sources of particulate carbon

    SciTech Connect

    Mazurek, M.A. ); Hildemann, L.M. . Dept. of Civil Engineering); Cass, G.R.; Rogge, W.F. ); Simoneit, B.R.T. . Coll. of Oceanography)

    1990-10-01

    Organic aerosols comprise approximately 30% by mass of the total fine particulate matter present in urban atmospheres. The chemical composition of such aerosols is complex and reflects input from multiple sources of primary emissions to the atmosphere, as well as from secondary production of carbonaceous aerosol species via photochemical reactions. To identify discrete sources of fine carbonaceous particles in urban atmospheres, analytical methods must reconcile both bulk chemical and molecular properties of the total carbonaceous aerosol fraction. This paper presents an overview of the analytical protocol developed and used in a study of the major sources of fine carbon particles emitted to an urban atmosphere. 23 refs., 1 fig., 2 tabs.

  13. High Diversity of Fungi in Air Particulate Matter

    NASA Astrophysics Data System (ADS)

    Fröhlich-Nowoisky, J.; Despres, V. R.; Pöschl, U.

    2009-04-01

    Fungal spores account for large proportions of air particulate matter, and they influence the hydrological cycle and climate as nuclei for water droplets and ice crystals in clouds, fog and precipitation. Moreover, some fungi are major pathogens and allergens. The diversity of airborne fungi is, however, hardly known. By DNA analysis we found pronounced differences in the relative abundance and seasonal cycles of various groups of fungi in coarse and fine particulate matter, with more plant pathogens in the coarse and more human pathogens and allergens in the respirable fine particle fraction (< 3 µm). Moreover, the ratio of Basidiomycota to Ascomycota was found to be much higher than previously assumed, which might also apply to the biosphere. References: Després, V.R., J.F. Nowoisky, M. Klose, R. Conrad, M.O. Andreae, U. Pöschl, Characterization of primary biogenic aerosol particles in urban, rural, and high-alpine air by DNA sequence and restriction fragment analysis of ribosomal RNA genes, Biogeosciences, 4, 1127-1141, 2007. Elbert, W., P. E. Taylor, M. O. Andreae, U. Pöschl, Contribution of fungi to primary biogenic aerosols in the atmosphere: wet and dry discharged spores, carbohydrates, and inorganic ions, Atmospheric Chemistry and Physics, 7, 4569-4588, 2007. Fröhlich-Nowoisky, J. Despres, V.R., Pöschl, U.: High diversity of fungi in air particulate matter, Proceedings of the National Academy of Sciences, submitted, 2008.

  14. 40 CFR 60.422 - Standards for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standards for particulate matter. 60... Manufacture § 60.422 Standards for particulate matter. On or after the date on which the performance test... sulfate dryer, particulate matter at an emission rate exceeding 0.15 kilogram of particulate per...

  15. 40 CFR 60.422 - Standards for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standards for particulate matter. 60... Manufacture § 60.422 Standards for particulate matter. On or after the date on which the performance test... sulfate dryer, particulate matter at an emission rate exceeding 0.15 kilogram of particulate per...

  16. 40 CFR 60.422 - Standards for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standards for particulate matter. 60... Manufacture § 60.422 Standards for particulate matter. On or after the date on which the performance test... sulfate dryer, particulate matter at an emission rate exceeding 0.15 kilogram of particulate per...

  17. Particulate matter formation from photochemical degradation of organophosphorus pesticides

    NASA Astrophysics Data System (ADS)

    Borrás, E.; Ródenas, M.; Vera, T.; Muñoz, A.

    2015-12-01

    Several experiments were performed in the European Photo-reactor - EUPHORE - for studying aerosol formation from organophosphorus pesticides such as diazinon, chlorpyrifos, chlorpyrifos-methyl and pirimiphos-methyl. The mass concentration yields obtained (Y) were in the range 5 - 44% for the photo-oxidation reactions in the presence and the absence of NOx. These results confirm the importance of studying pesticides as significant precursors of atmospheric particulate matter due to the serious risks associated to them. The studies based on the use of EUPHORE photoreactor provide useful data about atmospheric degradation processes of organophosphorus pesticides to the atmosphere. Knowledge of the specific degradation products, including the formation of secondary particulate matter, could complete the assessment of their potential impact, since the formation of those degradation products plays a significant role in the atmospheric chemistry, global climate change, radiative force, and are related to health effects.

  18. Particulate matter in the Venus atmosphere

    NASA Technical Reports Server (NTRS)

    Ragent, B.; Esposito, L. W.; Tomasko, M. G.; Marov, M. IA.; Shari, V. P.

    1985-01-01

    The paper presents a summary of the data currently available (June 1984) describing the planet-enshrouding particulate matter in the Venus atmosphere. A description and discussion of the state of knowledge of the Venus clouds and hazes precedes the tables and plots. The tabular material includes a precis of upper haze and cloud-top properties, parameters for model-size distributions for particles and particulate layers, and columnar masses and mass loadings.

  19. Particulate matter sensor with a heater

    DOEpatents

    Hall, Matthew

    2011-08-16

    An apparatus to detect particulate matter. The apparatus includes a sensor electrode, a shroud, and a heater. The electrode measures a chemical composition within an exhaust stream. The shroud surrounds at least a portion of the sensor electrode, exclusive of a distal end of the sensor electrode exposed to the exhaust stream. The shroud defines an air gap between the sensor electrode and the shroud and an opening toward the distal end of the sensor electrode. The heater is mounted relative to the sensor electrode. The heater burns off particulate matter in the air gap between the sensor electrode and the shroud.

  20. Long-term assessment of particulate matter using CHIMERE model

    NASA Astrophysics Data System (ADS)

    Monteiro, A.; Miranda, A. I.; Borrego, C.; Vautard, R.; Ferreira, J.; Perez, A. T.

    Particulate matter (PM) and aerosols have became a critical pollutant and object of several research applications, due to their increasing levels, especially in urban areas, causing air pollution problems and thus effects on human health. The main purpose of this study is to perform a first long-term air quality assessment for Portugal, regarding aerosols and PM pollution. The CHIMERE chemistry-transport model, forced by the MM5 meteorological fields, was applied over Portugal for 2001 year, with 10 km horizontal resolution, using an emission inventory obtained from a spatial top-down disaggregation of the 2001 national inventory database. The evaluation model exercise shows a model trend to overestimate particulate pollution episodes (peaks) at urban sites, especially in winter season. This could be due to an underprediction of the winter model vertical mixing and also to an overestimation of PM emissions. Simulated inorganic components (ammonium and sulfate) and secondary organic aerosols (SOA) were compared to measurements taken at Aveiro (northwest coast of Portugal). An underestimation of the three components was verified. However, the model is able to predict their seasonal variation. Nevertheless, as a first approach, and despite the complex topography and coastal location of Portugal affected by sea salt natural aerosols emissions, the results obtained show that the model reproduces the PM levels, temporal evolution, and spatial patterns. The concentration maps reveal that the areas with high PM values are covered by the air quality monitoring network.

  1. Airborne particulate matter in spacecraft

    NASA Technical Reports Server (NTRS)

    1988-01-01

    Acceptability limits and sampling and monitoring strategies for airborne particles in spacecraft were considered. Based on instances of eye and respiratory tract irritation reported by Shuttle flight crews, the following acceptability limits for airborne particles were recommended: for flights of 1 week or less duration (1 mg/cu m for particles less than 10 microns in aerodynamic diameter (AD) plus 1 mg/cu m for particles 10 to 100 microns in AD); and for flights greater than 1 week and up to 6 months in duration (0.2 mg/cu m for particles less than 10 microns in AD plus 0.2 mg/cu m for particles 10 to 100 microns in AD. These numerical limits were recommended to aid in spacecraft atmosphere design which should aim at particulate levels that are a low as reasonably achievable. Sampling of spacecraft atmospheres for particles should include size-fractionated samples of 0 to 10, 10 to 100, and greater than 100 micron particles for mass concentration measurement and elementary chemical analysis by nondestructive analysis techniques. Morphological and chemical analyses of single particles should also be made to aid in identifying airborne particulate sources. Air cleaning systems based on inertial collection principles and fine particle collection devices based on electrostatic precipitation and filtration should be considered for incorporation into spacecraft air circulation systems. It was also recommended that research be carried out in space in the areas of health effects and particle characterization.

  2. Miniature Sensors for Airborne Particulate Matter

    EPA Science Inventory

    Our group is working to design a small,lightweight, low-cost real-time particulate matter(PM) sensor to enable better monitoring of PMconcentrations in air, with the goal of informingpolicymakers and regulators to provide betterpublic health. The sensor reads the massconcentratio...

  3. SPATIAL PREDICTION OF FINE PARTICULATE MATTER

    EPA Science Inventory

    A new national monitoring network for the measurement of fine particular matter (PM2.5) is currently under development. A primary goal of this network is to collect monitoring data in residential communities for the evaluation of compliance with particulate air quality standards...

  4. REINVENTING PERSONAL EXPOSURE TO PARTICULATE MATTER

    EPA Science Inventory

    Recent epidemiologic studies of modern air pollution show statistically significant relationships between fluctuations of daily non-trauma mortality and fluctuations of daily ambient particulate matter (PM) levels at low concentrations. A review of historic smoke-fog (smog)episo...

  5. FINE PARTICULATE MATTER EMISSIONS FROM CANDLES

    EPA Science Inventory

    The paper gives reulst of testing five types of candles, purchased from local stores, for fine particulate matter (PM) emissions under close-to-realistic conditions in a research house. The test method allows for determination of both the emission and deposition rates. Most tes...

  6. Source apportionment of particulate matter in Denmark

    NASA Astrophysics Data System (ADS)

    Moenster, J.; Glasius, M.; Nielsen, O. J.; Bilde, M.; Jensen, F. P.

    2005-12-01

    Atmospheric particulate matter (PM) has received considerable attention over the last decade as an important component of air pollution, particularly due to its health effects on the exposed population. Typically the mass of particles with diameters smaller that 10 μm (PM10) has been used in large cohort studies to estimate health effects such as increase in hospitalization rate, asthma attacks and premature deaths. Particles smaller than 2.5 μm (PM2.5) and ultra fine particles have been used in various epidemiological studies and correlations between exposure to fine and ultra fine particles and health effects have been found. Limits of acceptable concentrations of PM10, PM2.5 and some carcinogenic species have been made, and it is important to find the origin of the particulate matter to prevent exceeds of these limits. This can be done by measuring particle mass, organic/inorganic fractions of particles, the chemical components and other relevant factors, and then use receptor modeling for source apportionment of the particulate matter. We have done measurements at street level and urban background in Copenhagen, Denmark, to determine the origin of different sizes of particulate matter and the toxic organic compounds connected to these particles. We also did measurements in a small village with less traffic and more residential wood combustion for a comparison between traffic and wood combustion generated pollution. Our results show a significant amount of particulate matter coming from non local sources and are dominated by long-range transported inorganic salts. The amount of these is highly depended on the wind direction and thus on the origin of the wind plume. The origin of the carcinogenic organic compound benzo(a)pyrene was found to be local combustion sources. To prevent events of high particulate matter concentration in Copenhagen, Denmark, a reduction of emission from the local traffic will only lead to a minor effect, since the majority of the

  7. Continuous measurements at the urban roadside in an Asian megacity by Aerosol Chemical Speciation Monitor (ACSM): particulate matter characteristics during fall and winter seasons in Hong Kong

    NASA Astrophysics Data System (ADS)

    Sun, C.; Lee, B. P.; Huang, D.; Jie Li, Y.; Schurman, M. I.; Louie, P. K. K.; Luk, C.; Chan, C. K.

    2016-02-01

    Non-refractory submicron aerosol is characterized using an Aerosol Chemical Speciation Monitor (ACSM) in the fall and winter seasons of 2013 on the roadside in an Asian megacity environment in Hong Kong. Organic aerosol (OA), characterized by application of Positive Matrix Factorization (PMF), and sulfate are found to be dominant. Traffic-related organic aerosol shows good correlation with other vehicle-related species, and cooking aerosol displays clear mealtime concentration maxima and association with surface winds from restaurant areas. Contributions of individual species and OA factors to high NR-PM1 are analyzed for hourly data and daily data; while cooking emissions in OA contribute to high hourly concentrations, particularly during mealtimes, secondary organic aerosol components are responsible for episodic events and high day-to-day PM concentrations. Clean periods are either associated with precipitation, which reduces secondary OA with a lesser impact on primary organics, or clean oceanic air masses with reduced long-range transport and better dilution of local pollution. Haze events are connected with increases in contribution of secondary organic aerosol, from 30 to 50 % among total non-refractory organics, and the influence of continental air masses.

  8. Continuous measurements at the urban roadside in an Asian Megacity by Aerosol Chemical Speciation Monitor (ACSM): particulate matter characteristics during fall and winter seasons in Hong Kong

    NASA Astrophysics Data System (ADS)

    Sun, C.; Lee, B. P.; Huang, D.; Li, Y. J.; Schurman, M. I.; Louie, P. K. K.; Luk, C.; Chan, C. K.

    2015-07-01

    Non-refractory submicron aerosol is characterized using an Aerosol Chemical Speciation Monitor (ACSM) in the fall and winter seasons of 2013 at the roadside in an Asian megacity environment in Hong Kong. Organic aerosol (OA), characterized by application of Positive Matrix Factorization (PMF), and sulfate are found dominant. Traffic-related organic aerosol shows good correlation with other vehicle-related species, and cooking aerosol displays clear meal-time concentration maxima and association with surface winds from restaurant areas. Contributions of individual species and OA factors to high NR-PM1 are analyzed for hourly data and daily data; while cooking emissions in OA contribute to high hourly concentrations, particularly during meal times, secondary organic aerosol components are responsible for episodic events and high day-to-day PM concentrations. Clean periods are either associated with precipitation, which reduces secondary OA with a~lesser impact on primary organics, or clean oceanic air masses with reduced long-range transport and better dilution of local pollution. Haze events are connected with increases in contribution of secondary organic aerosol, from 30 to 50 % among total non-refractory organics, and influence of continental air masses.

  9. 40 CFR 60.182 - Standard for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standard for particulate matter. 60.182... Smelters § 60.182 Standard for particulate matter. (a) On and after the date on which the performance test... furnace, or sintering machine discharge end any gases which contain particulate matter in excess of 50...

  10. 40 CFR 60.52 - Standard for particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standard for particulate matter. 60.52... § 60.52 Standard for particulate matter. (a) On and after the date on which the initial performance... atmosphere from any affected facility any gases which contain particulate matter in excess of 0.18 g/dscm...

  11. 40 CFR 60.122 - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.122... Smelters § 60.122 Standard for particulate matter. (a) On and after the date on which the performance test... furnace any gases which: (1) Contain particulate matter in excess of 50 mg/dscm (0.022 gr/dscf)....

  12. 40 CFR 52.2059 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Particulate matter... Control strategy: Particulate matter. (a) Pennsylvania has committed to undertake a comprehensive program... Investigating and Controlling Nontraditional Particulate Matter Emissions Task Completion date Scheduled...

  13. 40 CFR 60.282 - Standard for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standard for particulate matter. 60.282... § 60.282 Standard for particulate matter. (a) On and after the date on which the performance test...: (i) Contain particulate matter in excess of 0.10 g/dscm (0.044 gr/dscf) corrected to 8 percent...

  14. 40 CFR 60.92 - Standard for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standard for particulate matter. 60.92... Facilities § 60.92 Standard for particulate matter. (a) On and after the date on which the performance test... which: (1) Contain particulate matter in excess of 90 mg/dscm (0.04 gr/dscf). (2) Exhibit 20...

  15. 40 CFR 60.472 - Standards for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standards for particulate matter. 60... Processing and Asphalt Roofing Manufacture § 60.472 Standards for particulate matter. (a) On and after the...) Particulate matter in excess of: (i) 0.04 kg/Mg (0.08 lb/ton) of asphalt shingle or mineral-surfaced...

  16. 40 CFR 52.2584 - Control strategy; Particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 5 2012-07-01 2012-07-01 false Control strategy; Particulate matter... Control strategy; Particulate matter. (a) Part D—Disapproval—USEPA disapproves Regulation NR 154.11(7)(b... control strategy to attain and maintain the standards for particulate matter, because it does not...

  17. 40 CFR 60.52 - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.52... § 60.52 Standard for particulate matter. (a) On and after the date on which the initial performance... atmosphere from any affected facility any gases which contain particulate matter in excess of 0.18 g/dscm...

  18. 40 CFR 52.427 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 3 2014-07-01 2014-07-01 false Control strategy: Particulate matter...: Particulate matter. (a) Determination of attainment. EPA has determined, as of May 16, 2012, that based on... fine particulate matter (PM2.5) nonattainment area has attained the 2006 24-hour PM2.5 national...

  19. 40 CFR 60.472 - Standards for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standards for particulate matter. 60... Processing and Asphalt Roofing Manufacture § 60.472 Standards for particulate matter. (a) On and after the...) Particulate matter in excess of: (i) 0.04 kg/Mg (0.08 lb/ton) of asphalt shingle or mineral-surfaced...

  20. 40 CFR 52.2584 - Control strategy; Particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy; Particulate matter... Control strategy; Particulate matter. (a) Part D—Disapproval—USEPA disapproves Regulation NR 154.11(7)(b... control strategy to attain and maintain the standards for particulate matter, because it does not...

  1. 40 CFR 60.382 - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.382... Processing Plants § 60.382 Standard for particulate matter. (a) On and after the date on which the... stack emissions that: (1) Contain particulate matter in excess of 0.05 grams per dry standard...

  2. 40 CFR 60.172 - Standard for particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 7 2012-07-01 2012-07-01 false Standard for particulate matter. 60.172... Smelters § 60.172 Standard for particulate matter. (a) On and after the date on which the performance test... contain particulate matter in excess of 50 mg/dscm (0.022 gr/dscf)....

  3. 40 CFR 60.142a - Standards for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standards for particulate matter. 60... 20, 1983 § 60.142a Standards for particulate matter. (a) Except as provided under paragraphs (b) and...-blown BOPF and contain particulate matter in excess of 23 mg/dscm (0.010 gr/dscf). (3) Exit from...

  4. 40 CFR 52.427 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 3 2013-07-01 2013-07-01 false Control strategy: Particulate matter...: Particulate matter. (a) Determination of attainment. EPA has determined, as of May 16, 2012, that based on... fine particulate matter (PM2.5) nonattainment area has attained the 2006 24-hour PM2.5 national...

  5. 40 CFR 52.1476 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Control strategy: Particulate matter... strategy: Particulate matter. (a) The requirements of subpart G of this chapter are not met since the plan does not provide for the attainment and maintenance of the national standards for particulate matter...

  6. 40 CFR 60.182 - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.182... Smelters § 60.182 Standard for particulate matter. (a) On and after the date on which the performance test... furnace, or sintering machine discharge end any gases which contain particulate matter in excess of 50...

  7. 40 CFR 60.402 - Standard for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standard for particulate matter. 60.402... Plants § 60.402 Standard for particulate matter. (a) On and after the date on which the performance test... which: (i) Contain particulate matter in excess of 0.030 kilogram per megagram of phosphate rock feed...

  8. 40 CFR 60.292 - Standards for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standards for particulate matter. 60... Manufacturing Plants § 60.292 Standards for particulate matter. (a) On and after the date on which the..., particulate matter at emission rates exceeding those specified in table CC-1, Column 2 and Column...

  9. 40 CFR 52.1476 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Particulate matter... strategy: Particulate matter. (a) The requirements of subpart G of this chapter are not met since the plan does not provide for the attainment and maintenance of the national standards for particulate matter...

  10. 40 CFR 60.162 - Standard for particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standard for particulate matter. 60.162... Smelters § 60.162 Standard for particulate matter. (a) On and after the date on which the performance test... particulate matter in excess of 50 mg/dscm (0.022 gr/dscf)....

  11. 40 CFR 60.342 - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.342... Manufacturing Plants § 60.342 Standard for particulate matter. (a) On and after the date on which the... gases which: (1) Contain particulate matter in excess of 0.30 kilogram per megagram (0.60 lb/ton)...

  12. 40 CFR 52.2584 - Control strategy; Particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 5 2014-07-01 2014-07-01 false Control strategy; Particulate matter... Control strategy; Particulate matter. (a) Part D—Disapproval—USEPA disapproves Regulation NR 154.11(7)(b... control strategy to attain and maintain the standards for particulate matter, because it does not...

  13. 40 CFR 60.302 - Standard for particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 7 2012-07-01 2012-07-01 false Standard for particulate matter. 60.302... § 60.302 Standard for particulate matter. (a) On and after the 60th day of achieving the maximum... a grain dryer any process emission which: (1) Contains particulate matter in excess of 0.023...

  14. 40 CFR 52.776 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 3 2014-07-01 2014-07-01 false Control strategy: Particulate matter...: Particulate matter. (a) The requirements of subpart G of this chapter are not met since the plan does not provide for attainment and maintenance of the secondary standards for particulate matter in...

  15. 40 CFR 60.92 - Standard for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standard for particulate matter. 60.92... Facilities § 60.92 Standard for particulate matter. (a) On and after the date on which the performance test... which: (1) Contain particulate matter in excess of 90 mg/dscm (0.04 gr/dscf). (2) Exhibit 20...

  16. 40 CFR 52.2584 - Control strategy; Particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 5 2013-07-01 2013-07-01 false Control strategy; Particulate matter... Control strategy; Particulate matter. (a) Part D—Disapproval—USEPA disapproves Regulation NR 154.11(7)(b... control strategy to attain and maintain the standards for particulate matter, because it does not...

  17. 40 CFR 60.162 - Standard for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standard for particulate matter. 60.162... Smelters § 60.162 Standard for particulate matter. (a) On and after the date on which the performance test... particulate matter in excess of 50 mg/dscm (0.022 gr/dscf)....

  18. 40 CFR 60.272a - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60... Standard for particulate matter. (a) On and after the date of which the performance test required to be... control device and contain particulate matter in excess of 12 mg/dscm (0.0052 gr/dscf); (2) Exit from...

  19. 40 CFR 60.92 - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.92... Facilities § 60.92 Standard for particulate matter. (a) On and after the date on which the performance test... which: (1) Contain particulate matter in excess of 90 mg/dscm (0.04 gr/dscf). (2) Exhibit 20...

  20. 40 CFR 60.292 - Standards for particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 7 2012-07-01 2012-07-01 false Standards for particulate matter. 60... Manufacturing Plants § 60.292 Standards for particulate matter. (a) On and after the date on which the..., particulate matter at emission rates exceeding those specified in table CC-1, Column 2 and Column...

  1. 40 CFR 60.682 - Standard for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standard for particulate matter. 60.682... Insulation Manufacturing Plants § 60.682 Standard for particulate matter. On and after the date on which the... gases which contain particulate matter in excess of 5.5 kg/Mg (11.0 1b/ton) of glass pulled....

  2. 40 CFR 60.142a - Standards for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standards for particulate matter. 60... 20, 1983 § 60.142a Standards for particulate matter. (a) Except as provided under paragraphs (b) and...-blown BOPF and contain particulate matter in excess of 23 mg/dscm (0.010 gr/dscf). (3) Exit from...

  3. 40 CFR 60.182 - Standard for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standard for particulate matter. 60.182... Smelters § 60.182 Standard for particulate matter. (a) On and after the date on which the performance test... furnace, or sintering machine discharge end any gases which contain particulate matter in excess of 50...

  4. 40 CFR 60.282 - Standard for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standard for particulate matter. 60.282... § 60.282 Standard for particulate matter. (a) On and after the date on which the performance test...: (i) Contain particulate matter in excess of 0.10 g/dscm (0.044 gr/dscf) corrected to 8 percent...

  5. 40 CFR 60.162 - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.162... Smelters § 60.162 Standard for particulate matter. (a) On and after the date on which the performance test... particulate matter in excess of 50 mg/dscm (0.022 gr/dscf)....

  6. 40 CFR 60.92 - Standard for particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standard for particulate matter. 60.92... Facilities § 60.92 Standard for particulate matter. (a) On and after the date on which the performance test... which: (1) Contain particulate matter in excess of 90 mg/dscm (0.04 gr/dscf). (2) Exhibit 20...

  7. 40 CFR 60.342 - Standard for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standard for particulate matter. 60.342... Manufacturing Plants § 60.342 Standard for particulate matter. (a) On and after the date on which the... gases which: (1) Contain particulate matter in excess of 0.30 kilogram per megagram (0.60 lb/ton)...

  8. 40 CFR 60.182 - Standard for particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standard for particulate matter. 60.182... Smelters § 60.182 Standard for particulate matter. (a) On and after the date on which the performance test... furnace, or sintering machine discharge end any gases which contain particulate matter in excess of 50...

  9. 40 CFR 60.282 - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.282... § 60.282 Standard for particulate matter. (a) On and after the date on which the performance test...: (i) Contain particulate matter in excess of 0.10 g/dscm (0.044 gr/dscf) corrected to 8 percent...

  10. 40 CFR 60.682 - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.682... Insulation Manufacturing Plants § 60.682 Standard for particulate matter. On and after the date on which the... gases which contain particulate matter in excess of 5.5 kg/Mg (11.0 1b/ton) of glass pulled....

  11. 40 CFR 52.1476 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Particulate matter... strategy: Particulate matter. (a) The requirements of subpart G of this chapter are not met since the plan does not provide for the attainment and maintenance of the national standards for particulate matter...

  12. 40 CFR 52.776 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 3 2012-07-01 2012-07-01 false Control strategy: Particulate matter...: Particulate matter. (a) The requirements of subpart G of this chapter are not met since the plan does not provide for attainment and maintenance of the secondary standards for particulate matter in...

  13. 40 CFR 52.1476 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Particulate matter... strategy: Particulate matter. (a) The requirements of subpart G of this chapter are not met since the plan does not provide for the attainment and maintenance of the national standards for particulate matter...

  14. 40 CFR 60.172 - Standard for particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standard for particulate matter. 60.172... Smelters § 60.172 Standard for particulate matter. (a) On and after the date on which the performance test... contain particulate matter in excess of 50 mg/dscm (0.022 gr/dscf)....

  15. 40 CFR 60.162 - Standard for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standard for particulate matter. 60.162... Smelters § 60.162 Standard for particulate matter. (a) On and after the date on which the performance test... particulate matter in excess of 50 mg/dscm (0.022 gr/dscf)....

  16. 40 CFR 60.302 - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.302... § 60.302 Standard for particulate matter. (a) On and after the 60th day of achieving the maximum... a grain dryer any process emission which: (1) Contains particulate matter in excess of 0.023...

  17. 40 CFR 60.342 - Standard for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standard for particulate matter. 60.342... Manufacturing Plants § 60.342 Standard for particulate matter. (a) On and after the date on which the... gases which: (1) Contain particulate matter in excess of 0.30 kilogram per megagram (0.60 lb/ton)...

  18. 40 CFR 60.402 - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.402... Plants § 60.402 Standard for particulate matter. (a) On and after the date on which the performance test... which: (i) Contain particulate matter in excess of 0.030 kilogram per megagram of phosphate rock feed...

  19. 40 CFR 60.142a - Standards for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standards for particulate matter. 60... 20, 1983 § 60.142a Standards for particulate matter. (a) Except as provided under paragraphs (b) and...-blown BOPF and contain particulate matter in excess of 23 mg/dscm (0.010 gr/dscf). (3) Exit from...

  20. 40 CFR 60.282 - Standard for particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 7 2012-07-01 2012-07-01 false Standard for particulate matter. 60.282... § 60.282 Standard for particulate matter. (a) On and after the date on which the performance test...: (i) Contain particulate matter in excess of 0.10 g/dscm (0.044 gr/dscf) corrected to 8 percent...

  1. 40 CFR 52.2059 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Particulate matter... Control strategy: Particulate matter. (a) Pennsylvania has committed to undertake a comprehensive program... Investigating and Controlling Nontraditional Particulate Matter Emissions Task Completion date Scheduled...

  2. 40 CFR 52.776 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 3 2011-07-01 2011-07-01 false Control strategy: Particulate matter...: Particulate matter. (a) The requirements of subpart G of this chapter are not met since the plan does not provide for attainment and maintenance of the secondary standards for particulate matter in...

  3. 40 CFR 52.776 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 3 2013-07-01 2013-07-01 false Control strategy: Particulate matter...: Particulate matter. Link to an amendment published at 78 FR 28507, May 15, 2013. (a) The requirements of... the secondary standards for particulate matter in the Metropolitan Indianapolis Intrastate Region....

  4. 40 CFR 60.92 - Standard for particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 7 2012-07-01 2012-07-01 false Standard for particulate matter. 60.92... Facilities § 60.92 Standard for particulate matter. (a) On and after the date on which the performance test... which: (1) Contain particulate matter in excess of 90 mg/dscm (0.04 gr/dscf). (2) Exhibit 20...

  5. 40 CFR 60.302 - Standard for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standard for particulate matter. 60.302... § 60.302 Standard for particulate matter. (a) On and after the 60th day of achieving the maximum... a grain dryer any process emission which: (1) Contains particulate matter in excess of 0.023...

  6. 40 CFR 52.2059 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 5 2012-07-01 2012-07-01 false Control strategy: Particulate matter... Control strategy: Particulate matter. (a) Pennsylvania has committed to undertake a comprehensive program... Investigating and Controlling Nontraditional Particulate Matter Emissions Task Completion date Scheduled...

  7. 40 CFR 60.52 - Standard for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standard for particulate matter. 60.52... § 60.52 Standard for particulate matter. (a) On and after the date on which the initial performance... atmosphere from any affected facility any gases which contain particulate matter in excess of 0.18 g/dscm...

  8. 40 CFR 60.142a - Standards for particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 7 2012-07-01 2012-07-01 false Standards for particulate matter. 60... 20, 1983 § 60.142a Standards for particulate matter. (a) Except as provided under paragraphs (b) and...-blown BOPF and contain particulate matter in excess of 23 mg/dscm (0.010 gr/dscf). (3) Exit from...

  9. 40 CFR 60.292 - Standards for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standards for particulate matter. 60... Manufacturing Plants § 60.292 Standards for particulate matter. (a) On and after the date on which the..., particulate matter at emission rates exceeding those specified in table CC-1, Column 2 and Column...

  10. 40 CFR 60.162 - Standard for particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 7 2012-07-01 2012-07-01 false Standard for particulate matter. 60.162... Smelters § 60.162 Standard for particulate matter. (a) On and after the date on which the performance test... particulate matter in excess of 50 mg/dscm (0.022 gr/dscf)....

  11. 40 CFR 52.2059 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 5 2013-07-01 2013-07-01 false Control strategy: Particulate matter... Control strategy: Particulate matter. (a) Pennsylvania has committed to undertake a comprehensive program... Investigating and Controlling Nontraditional Particulate Matter Emissions Task Completion date Scheduled...

  12. 40 CFR 60.182 - Standard for particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 7 2012-07-01 2012-07-01 false Standard for particulate matter. 60.182... Smelters § 60.182 Standard for particulate matter. (a) On and after the date on which the performance test... furnace, or sintering machine discharge end any gases which contain particulate matter in excess of 50...

  13. 40 CFR 60.302 - Standard for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standard for particulate matter. 60.302... § 60.302 Standard for particulate matter. (a) On and after the 60th day of achieving the maximum... a grain dryer any process emission which: (1) Contains particulate matter in excess of 0.023...

  14. 40 CFR 60.52 - Standard for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standard for particulate matter. 60.52... § 60.52 Standard for particulate matter. (a) On and after the date on which the initial performance... atmosphere from any affected facility any gases which contain particulate matter in excess of 0.18 g/dscm...

  15. 40 CFR 52.2584 - Control strategy; Particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy; Particulate matter... Control strategy; Particulate matter. (a) Part D—Disapproval—USEPA disapproves Regulation NR 154.11(7)(b... control strategy to attain and maintain the standards for particulate matter, because it does not...

  16. 40 CFR 60.132 - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.132... and Bronze Production Plants § 60.132 Standard for particulate matter. (a) On and after the date on... reverberatory furnace any gases which: (1) Contain particulate matter in excess of 50 mg/dscm (0.022...

  17. 40 CFR 60.402 - Standard for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standard for particulate matter. 60.402... Plants § 60.402 Standard for particulate matter. (a) On and after the date on which the performance test... which: (i) Contain particulate matter in excess of 0.030 kilogram per megagram of phosphate rock feed...

  18. 40 CFR 60.52 - Standard for particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 7 2012-07-01 2012-07-01 false Standard for particulate matter. 60.52... § 60.52 Standard for particulate matter. (a) On and after the date on which the initial performance... atmosphere from any affected facility any gases which contain particulate matter in excess of 0.18 g/dscm...

  19. 40 CFR 60.682 - Standard for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standard for particulate matter. 60.682... Insulation Manufacturing Plants § 60.682 Standard for particulate matter. On and after the date on which the... gases which contain particulate matter in excess of 5.5 kg/Mg (11.0 1b/ton) of glass pulled....

  20. 40 CFR 60.292 - Standards for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standards for particulate matter. 60... Manufacturing Plants § 60.292 Standards for particulate matter. (a) On and after the date on which the..., particulate matter at emission rates exceeding those specified in table CC-1, Column 2 and Column...

  1. 40 CFR 52.2059 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 5 2014-07-01 2014-07-01 false Control strategy: Particulate matter... Control strategy: Particulate matter. (a) (b) EPA approves the PM-10 attainment demonstration for the...-Wilmington, PA-NJ-DE fine particulate matter (PM2.5) nonattainment area has attained the 2006 24-hour...

  2. Hyphenation of a EC / OC thermal-optical carbon analyzer to photo ionization time-of-flight mass spectrometry: a new off-line aerosol mass spectrometric approach for characterization of primary and secondary particulate matter

    NASA Astrophysics Data System (ADS)

    Diab, J.; Streibel, T.; Cavalli, F.; Lee, S. C.; Saathoff, H.; Mamakos, T.; Chow, J. C.; Chen, L.-W. A.; Watson, J. G.; Sippula, O.; Zimmermann, R.

    2015-01-01

    Source apportionment and exposure of primary and secondary aerosols remains a challenging research field. In particular, the organic composition of primary particles and the formation mechanism of secondary organic aerosols (SOA) warrant further investigations. Progress in this field is strongly connected to the development of novel analytical techniques. In this study an off-line aerosol mass spectrometric technique based on filter samples, a hyphenated thermal/optical analyzer-photo ionization time of flight mass spectrometer (PI-TOFMS) system, was developed. The approach extends the capability of the widely used PM carbon analysis (for elemental/organic carbon (EC / OC)) by enabling the investigation of evolved gaseous species with soft and selective (resonance enhanced multiphoton ionization, REMPI) and non-selective photo ionization (single photon ionization, SPI) techniques. SPI was tuned to be medium soft to achieve comparability with results obtained by electron ionization (EI) aerosol mass spectrometer (AMS). Different PM samples including wood combustion emission samples, smog chamber samples from the reaction of ozone with different SOA precursors, and ambient samples taken at Ispra, Italy in winter as well as in summer were tested. The EC / OC-PI-TOFMS technique increases the understanding of the processes during the thermal/optical analysis and identifies marker substances for the source apportionment. Composition of oligomeric or polymeric species present in PM can be investigated by the analysis of the thermally breakdown products. In case of wood combustion, in addition to the well-known markers at m/z ratios of 60 and 73, two new characteristic masses (m/z 70 and 98) have been revealed as potentially linked to biomass burning. All four masses were also the dominant signals in an ambient sample taken in winter time in Ispra, Italy, confirming the finding that wood burning for residential heating is a major source for particulate matter (PM) in

  3. Hyphenation of a EC / OC thermal-optical carbon analyzer to photo-ionization time-of-flight mass spectrometry: an off-line aerosol mass spectrometric approach for characterization of primary and secondary particulate matter

    NASA Astrophysics Data System (ADS)

    Diab, J.; Streibel, T.; Cavalli, F.; Lee, S. C.; Saathoff, H.; Mamakos, A.; Chow, J. C.; Chen, L.-W. A.; Watson, J. G.; Sippula, O.; Zimmermann, R.

    2015-08-01

    Source apportionment and characterization of primary and secondary aerosols remains a challenging research field. In particular, the organic composition of primary particles and the formation mechanism of secondary organic aerosols (SOAs) warrant further investigations. Progress in this field is strongly connected to the development of novel analytical techniques. In this study an off-line aerosol mass spectrometric technique based on filter samples, a hyphenated thermal-optical analyzer photo-ionization time-of-flight mass spectrometer (PI-TOFMS) system, was developed. The approach extends the capability of the widely used particulate matter (PM) carbon analysis (for elemental / organic carbon, EC / OC) by enabling the investigation of evolved gaseous species with soft and selective (resonance enhanced multi-photon ionization, REMPI) and non-selective photo-ionization (single-photon ionization, SPI) techniques. SPI was tuned to be medium soft to achieve comparability with results obtained by the electron ionization aerosol mass spectrometer (AMS). Different PM samples including wood combustion emission samples, smog chamber samples from the reaction of ozone with different SOA precursors, and ambient samples taken at Ispra, Italy, in winter as well as in summer were tested. The EC / OC-PI-TOFMS technique increases the understanding of the processes during thermal-optical analysis and identifies marker substances for the source apportionment. Composition of oligomeric or polymeric species present in PM can be investigated by the analysis of the thermal breakdown products. In the case of wood combustion, in addition to the well-known markers at m/z ratios of 60 and 73, two new characteristic masses (m/z 70 and 98) have been revealed as potentially linked to biomass burning. All four masses were also the dominant signals in an ambient sample taken in winter time in Ispra, Italy, confirming the finding that wood burning for residential heating is a major source of PM

  4. Establishing the origin of particulate matter across Europe

    NASA Astrophysics Data System (ADS)

    Schaap, Martijn; Kranenburg, Richard; Hendriks, Carlijn; Kuenen, Jeroen

    2016-04-01

    Exposure to particulate matter (PM) in ambient air leads to adverse health effects. To design cost effective mitigation strategies, a thorough understanding of the sources of particulate matter is crucial. In this paper we like to provide an overview of recent source apportionment studies aimed at PM and its precursors carried out at TNO. The source apportionment module that tracks the origin of modelled particulate matter distributions throughout a LOTOS-EUROS simulation will be explained. To optimally apply this technology dedicated emission inventories, e.g. fuel type specific, need to be generated. Applications to Europe shows that in northwestern Europe the contribution of transport and agricultural emissions dominate the PM mass concentrations, especially during episodic events. In eastern Europe, the domestic and energy sector are much more important. In southern Europe the picture is more mixed, although the frequent high levels of desert dust stand out. Evaluation of the source allocation against experimental data and PMF analyses is challenging as there is only a limited availability of source specific tracers or factors that can be used for direct comparison. Nonetheless, for the available tracers such as vanadium for heavy fuel oil combustion an evaluation is very well possible. The source apportionment technique can also be used to interpret particulate matter formation efficiencies. It will be shown that the conversion rates for the secondary inorganic aerosol precursors (NOx, NH3 and SO2) have changed during the last 20 years. A particular problem is related to the fact that CTMs systematically underestimate observed PM levels, which means that the contribution of certain source categories (natural, agriculture, combustion) are underestimated. Future developments needed to improve the source apportionment information concerning process knowledge, data assimilation as well as model implementation will be discussed. Specific challenges concerning the

  5. Thermogravimetric analysis of diesel particulate matter

    NASA Astrophysics Data System (ADS)

    Lapuerta, M.; Ballesteros, R.; Rodríguez-Fernández, J.

    2007-03-01

    The regulated level of diesel particulate mass for 2008 light-duty diesel on-road engines will be 0.005 g km-1 in Europe. Measurements by weighing and analysis of this low level of particulate mass based on chemical extraction are costly, time consuming and hazardous because of the use of organic solvents, potentially carcinogenic. An alternative to this analysis is proposed here: a thermal mass analyser that measures the volatile fraction (VOF) as well as the soot fraction of the particulate matter (PM) collected on a cleaned fibre glass filter. This paper evaluates this new thermal mass measurement (TGA) as a possible alternative to the conventional chemical extraction method, and presents the results obtained with both methods when testing a diesel engine fuelled with a reference diesel fuel (REF), a pure biodiesel fuel (B100) and two blends with 30% and 70% v/v biodiesel (B30 and B70, respectively).

  6. NICKEL SPECIATION OF URBAN PARTICULATE MATTER

    SciTech Connect

    Kevin C. Galbreath; Charlene R. Crocker; Carolyn M. Nyberg; Frank E. Huggins; Gerald P. Huffman

    2003-10-01

    A four-step sequential Ni extraction method, summarized in Table AB-1, was evaluated for identifying and quantifying the Ni species occurring in urban total suspended particulate (TSP) matter and fine particulate matter (<10 {micro}m [PM{sub 10}] and <2.5 {micro}m [PM{sub 2.5}] in aerodynamic diameter). The extraction method was originally developed for quantifying soluble, sulfidic, elemental, and oxidic forms of Ni that may occur in industrial atmospheres. X-ray diffraction (XRD) and x-ray absorption fine structure (XAFS) spectroscopy were used to evaluate the Ni species selectivity of the extraction method. Uncertainties in the chemical speciation of Ni in urban PM{sub 10} and PM{sub 2.5} greatly affect inhalation health risk estimates, primarily because of the large variability in acute, chronic, and cancer-causing effects for different Ni compounds.

  7. Characterization of iron in airborne particulate matter

    NASA Astrophysics Data System (ADS)

    Tavares, F. V. F.; Ardisson, J. D.; Rodrigues, P. C. H.; Brito, W.; Macedo, W. A. A.; Jacomino, V. M. F.

    2014-01-01

    In this work soil samples, iron ore and airborne atmospheric particulate matter (PM) in the Metropolitan Region of Belo Horizonte (MRBH), State of Minas Gerais, Brazil, are investigated with the aim of identifying if the sources of the particulate matter are of natural origin, such as, resuspension of particles from soil, or due to anthropogenic origins from mining and processing of iron ore. Samples were characterized by powder X-ray diffraction, X-ray fluorescence and 57Fe-Mössbauer spectroscopy. The results showed that soil samples studied are rich in quartz and have low contents of iron mainly iron oxide with low crystallinity. The samples of iron ore and PM have high concentration of iron, predominantly well crystallized hematite. 57Fe-Mössbauer spectroscopy confirmed the presence of similar iron oxides in samples of PM and in the samples of iron ore, indicating the anthropogenic origin in the material present in atmosphere of the study area.

  8. PARTICULATE MATTER NAAQS RISK AND EXPOSURE ...

    EPA Pesticide Factsheets

    The PM REA assesses human exposure and health risks for particulate matter. To provide a quantitative assessment of PM exposures and health risks as one of the key information inputs to the Administrator in order to make an informed decision regarding the PM NAAQS. A tiered risk/exposure assessment will be conducted as part of the PM NAAQS review and will be peer reviewed by the Clean Air Scientific Advisory Committee (CASAC) of EPA’s Science Advisory Board.

  9. Aromatic Radicals-Acetylene Particulate Matter Chemistry

    DTIC Science & Technology

    2011-12-01

    atmosphere1. In addition to acute respiratory problems, long-term effects include lung cancer and cardiopulmonary diseases , as studied by Pope at al...problems such as ischemic heart disease , fatal arrhythmia, and congestive heart failure4,5. Strategies to reduce fine particulate matter (PM...acetylene reaction have been made by Fahr and Stein15, who deduced an Arrhenius expression in a 4 temperature range between 1000 and 1330 K in

  10. High secondary aerosol contribution to particulate pollution during haze events in China

    NASA Astrophysics Data System (ADS)

    Huang, Ru-Jin; Zhang, Yanlin; Bozzetti, Carlo; Ho, Kin-Fai; Cao, Jun-Ji; Han, Yongming; Daellenbach, Kaspar R.; Slowik, Jay G.; Platt, Stephen M.; Canonaco, Francesco; Zotter, Peter; Wolf, Robert; Pieber, Simone M.; Bruns, Emily A.; Crippa, Monica; Ciarelli, Giancarlo; Piazzalunga, Andrea; Schwikowski, Margit; Abbaszade, Gülcin; Schnelle-Kreis, Jürgen; Zimmermann, Ralf; An, Zhisheng; Szidat, Sönke; Baltensperger, Urs; Haddad, Imad El; Prévôt, André S. H.

    2014-10-01

    Rapid industrialization and urbanization in developing countries has led to an increase in air pollution, along a similar trajectory to that previously experienced by the developed nations. In China, particulate pollution is a serious environmental problem that is influencing air quality, regional and global climates, and human health. In response to the extremely severe and persistent haze pollution experienced by about 800 million people during the first quarter of 2013 (refs 4, 5), the Chinese State Council announced its aim to reduce concentrations of PM2.5 (particulate matter with an aerodynamic diameter less than 2.5 micrometres) by up to 25 per cent relative to 2012 levels by 2017 (ref. 6). Such efforts however require elucidation of the factors governing the abundance and composition of PM2.5, which remain poorly constrained in China. Here we combine a comprehensive set of novel and state-of-the-art offline analytical approaches and statistical techniques to investigate the chemical nature and sources of particulate matter at urban locations in Beijing, Shanghai, Guangzhou and Xi'an during January 2013. We find that the severe haze pollution event was driven to a large extent by secondary aerosol formation, which contributed 30-77 per cent and 44-71 per cent (average for all four cities) of PM2.5 and of organic aerosol, respectively. On average, the contribution of secondary organic aerosol (SOA) and secondary inorganic aerosol (SIA) are found to be of similar importance (SOA/SIA ratios range from 0.6 to 1.4). Our results suggest that, in addition to mitigating primary particulate emissions, reducing the emissions of secondary aerosol precursors from, for example, fossil fuel combustion and biomass burning is likely to be important for controlling China's PM2.5 levels and for reducing the environmental, economic and health impacts resulting from particulate pollution.

  11. High secondary aerosol contribution to particulate pollution during haze events in China.

    PubMed

    Huang, Ru-Jin; Zhang, Yanlin; Bozzetti, Carlo; Ho, Kin-Fai; Cao, Jun-Ji; Han, Yongming; Daellenbach, Kaspar R; Slowik, Jay G; Platt, Stephen M; Canonaco, Francesco; Zotter, Peter; Wolf, Robert; Pieber, Simone M; Bruns, Emily A; Crippa, Monica; Ciarelli, Giancarlo; Piazzalunga, Andrea; Schwikowski, Margit; Abbaszade, Gülcin; Schnelle-Kreis, Jürgen; Zimmermann, Ralf; An, Zhisheng; Szidat, Sönke; Baltensperger, Urs; El Haddad, Imad; Prévôt, André S H

    2014-10-09

    Rapid industrialization and urbanization in developing countries has led to an increase in air pollution, along a similar trajectory to that previously experienced by the developed nations. In China, particulate pollution is a serious environmental problem that is influencing air quality, regional and global climates, and human health. In response to the extremely severe and persistent haze pollution experienced by about 800 million people during the first quarter of 2013 (refs 4, 5), the Chinese State Council announced its aim to reduce concentrations of PM2.5 (particulate matter with an aerodynamic diameter less than 2.5 micrometres) by up to 25 per cent relative to 2012 levels by 2017 (ref. 6). Such efforts however require elucidation of the factors governing the abundance and composition of PM2.5, which remain poorly constrained in China. Here we combine a comprehensive set of novel and state-of-the-art offline analytical approaches and statistical techniques to investigate the chemical nature and sources of particulate matter at urban locations in Beijing, Shanghai, Guangzhou and Xi'an during January 2013. We find that the severe haze pollution event was driven to a large extent by secondary aerosol formation, which contributed 30-77 per cent and 44-71 per cent (average for all four cities) of PM2.5 and of organic aerosol, respectively. On average, the contribution of secondary organic aerosol (SOA) and secondary inorganic aerosol (SIA) are found to be of similar importance (SOA/SIA ratios range from 0.6 to 1.4). Our results suggest that, in addition to mitigating primary particulate emissions, reducing the emissions of secondary aerosol precursors from, for example, fossil fuel combustion and biomass burning is likely to be important for controlling China's PM2.5 levels and for reducing the environmental, economic and health impacts resulting from particulate pollution.

  12. TOXICOLOGICAL EFFECTS OF PARTICULATE MATTER DERIVED FROM THE DESTRUCTION OF THE WORLD TRADE CENTER

    EPA Science Inventory

    May 15, 2002
    Abstract submitted by Stephen H. Gavett for American Association for Aerosol Research (AAAR) annual meeting October 7-11, 2002 in Charlotte, NC.

    TOXICOLOGICAL EFFECTS OF PARTICULATE MATTER DERIVED FROM THE DESTRUCTION OF THE WORLD TRADE CENTER
    Stephen H ...

  13. An evaluation of indoor and outdoor biological particulate matter (BioPM)

    EPA Science Inventory

    Monitoring of indoor and ambient particulate matter (PM) and the characterization of the content for biological aerosol concentrations has not been extensively performed. Samples from urban and rural North Carolina, and Denver, CO, were collected and analyzed as the goal of this ...

  14. Particulate matter and black carbon optical properties and emission factors from prescribed fires in the southeastern United States

    EPA Science Inventory

    The aerosol emissions from prescribed fires in the Southeastern United States were measured and compared to emissions from laboratory burns with fuels collected from the site. Fine particulate matter (PM2.5), black carbon, and aerosol light scattering and absorption were characte...

  15. Characterization of Particulate Matter from a Heavily Industrial Environment

    NASA Astrophysics Data System (ADS)

    Valarini, Simone; Ynoue, Rita Yuri

    2011-01-01

    A characterization of PM aerosols collected in Cubatão, Brazil is presented. Throughout 2009, 5 sampling campaings were carried out at CEPEMA (Centro de Capacitação e Pesquisa em Meio Ambiente da Universidade de São Paulo), in the vicinity of PETROBRAS oil refinery. Mini-vol portable air sampler was deployed to collect coarse and fine particles. Size-fractionated particle samples were collected by a Micro-Orifice Uniform Deposition Impactor (MOUDI) device. Gravimetric analysis showed three peaks for mass size distributions: the After-Filter stage (cut point diameter of less than 0,1μm), stage 7A (d=0,32μm) and stage 3A (d= 3,2μm). Fine particle matter (FPM) concentrations were almost always lower than coarse particle matter (CPM) concentrations. Comparison between the PM2.5 (particulate matter lower than 2.5μg.m-3) measurements by the MOUDI and Mini-Vol sampler reveals good agreement. However, MOUDI underestimates CPM. Reflectance analysis showed that almost all the Black Carbon is found in the Mini-Vol FPM and lower stages of the MOUDI, with higher concentrations at the After-Filter. The atmospheric loading of PM 2.5 was elevated at night, mainly due to more stable atmospheric conditions. Aerosol samples were analyzed for water- soluble ions, black carbon (BC), and trace elements using a number of analytical techniques.

  16. Micro-scale variability of particulate matter and the influence of urban fabric on the aerosol distribution in two mid-sized German cities

    NASA Astrophysics Data System (ADS)

    Paas, Bastian; Schneider, Christoph

    2016-04-01

    Spatial micro-scale variability of particle mass concentrations is an important criterion for urban air quality assessment. The major proportion of the world's population lives in cities, where exceedances of air quality standards occur regularly. Current research suggests that both long-term and even short-term stays, e.g. during commuting or relaxing, at locations with high PM concentrations could have significant impacts on health. In this study we present results from model calculations in comparison to high resolution spatial and temporal measurements. Airborne particles were sampled using an optical particle counter in two inner-city park areas in Aachen and Munster. Both are mid-sized German cities which, however, are characterized by a different topology. The measurement locations represent spots with different degrees of outdoor particle exposure that can be experienced by a pedestrian walking in an intra-urban recreational area. Simulations of aerosol distributions induced by road traffic were conducted using both the German reference dispersion model Austal2000 and the numerical microclimate model ENVI-met. Simulation results reveal details in the distribution of urban particles with highest concentrations of PM10 in direct vicinity to traffic lines. The corresponding concentrations rapidly decline as the distances to the line sources increase. Still, urban fabric and obstacles like shrubs or trees are proved to have a major impact on the aerosol distribution in the area. Furthermore, the distribution of particles was highly dependent of wind direction and turbulence characteristics. The analysis of observational data leads to the hypothesis that besides motor traffic numerous diffuse particle sources e.g. on the ability of surfaces to release particles by resuspension which were dominantly apparent in measured PM(1;10) and PM(0.25;10) data are present in the urban roughness layer. The results highlight that a conclusive picture concerning micro

  17. 40 CFR 52.1880 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Control strategy: Particulate matter... strategy: Particulate matter. (a) The requirements of subpart G of this chapter are not met because the... matter in the Greater Metropolitan Cleveland Intrastate Region and the Ohio portions of the...

  18. 40 CFR 52.1880 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Particulate matter... strategy: Particulate matter. (a) The requirements of subpart G of this chapter are not met because the... matter in the Greater Metropolitan Cleveland Intrastate Region and the Ohio portions of the...

  19. 40 CFR 52.1880 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Particulate matter... strategy: Particulate matter. (a) The requirements of subpart G of this chapter are not met because the... matter in the Greater Metropolitan Cleveland Intrastate Region and the Ohio portions of the...

  20. 40 CFR 52.1880 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Particulate matter... strategy: Particulate matter. (a) The requirements of subpart G of this chapter are not met because the... matter in the Greater Metropolitan Cleveland Intrastate Region and the Ohio portions of the...

  1. Organic speciation of size-segregated atmospheric particulate matter

    NASA Astrophysics Data System (ADS)

    Tremblay, Raphael

    Particle size and composition are key factors controlling the impacts of particulate matter (PM) on human health and the environment. A comprehensive method to characterize size-segregated PM organic content was developed, and evaluated during two field campaigns. Size-segregated particles were collected using a cascade impactor (Micro-Orifice Uniform Deposit Impactor) and a PM2.5 large volume sampler. A series of alkanes and polycyclic aromatic hydrocarbons (PAHs) were solvent extracted and quantified using a gas chromatograph coupled with a mass spectrometer (GC/MS). Large volume injections were performed using a programmable temperature vaporization (PTV) inlet to lower detection limits. The developed analysis method was evaluated during the 2001 and 2002 Intercomparison Exercise Program on Organic Contaminants in PM2.5 Air Particulate Matter led by the US National Institute of Standards and Technology (NIST). Ambient samples were collected in May 2002 as part of the Tampa Bay Regional Atmospheric Chemistry Experiment (BRACE) in Florida, USA and in July and August 2004 as part of the New England Air Quality Study - Intercontinental Transport and Chemical Transformation (NEAQS - ITCT) in New Hampshire, USA. Morphology of the collected particles was studied using scanning electron microscopy (SEM). Smaller particles (one micrometer or less) appeared to consist of solid cores surrounded by a liquid layer which is consistent with combustion particles and also possibly with particles formed and/or coated by secondary material like sulfate, nitrate and secondary organic aerosols. Source apportionment studies demonstrated the importance of stationary sources on the organic particulate matter observed at these two rural sites. Coal burning and biomass burning were found to be responsible for a large part of the observed PAHs during the field campaigns. Most of the measured PAHs were concentrated in particles smaller than one micrometer and linked to combustion sources

  2. 40 CFR 60.152 - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.152... Plants § 60.152 Standard for particulate matter. (a) On and after the date on which the performance test...: (1) Particulate matter at a rate in excess of 0.65 g/kg dry sludge input (1.30 lb/ton dry...

  3. 40 CFR 60.152 - Standard for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standard for particulate matter. 60.152... Plants § 60.152 Standard for particulate matter. (a) On and after the date on which the performance test...: (1) Particulate matter at a rate in excess of 0.65 g/kg dry sludge input (1.30 lb/ton dry...

  4. 40 CFR 60.152 - Standard for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standard for particulate matter. 60.152... Plants § 60.152 Standard for particulate matter. (a) On and after the date on which the performance test...: (1) Particulate matter at a rate in excess of 0.65 g/kg dry sludge input (1.30 lb/ton dry...

  5. 40 CFR 60.152 - Standard for particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standard for particulate matter. 60.152... Plants § 60.152 Standard for particulate matter. (a) On and after the date on which the performance test...: (1) Particulate matter at a rate in excess of 0.65 g/kg dry sludge input (1.30 lb/ton dry...

  6. 40 CFR 60.152 - Standard for particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 7 2012-07-01 2012-07-01 false Standard for particulate matter. 60.152... Plants § 60.152 Standard for particulate matter. (a) On and after the date on which the performance test...: (1) Particulate matter at a rate in excess of 0.65 g/kg dry sludge input (1.30 lb/ton dry...

  7. Assessing the Cytotoxicity of Black Carbon As A Model for Ultrafine Anthropogenic Aerosol Across Human and Murine Cells: A Chronic Exposure Model of Nanosized Particulate Matter

    NASA Astrophysics Data System (ADS)

    Salinas, E.

    2015-12-01

    Combustion-derived nanomaterials or ultrafine (<1 μm) atmospheric aerosols are primarily products of anthropogenic activities, such as the burning of fossil fuels. Ultrafine particles (UFPs) can absorb other noxious pollutants including volatile organic compounds (VOCs), polycyclic aromatic hydrocarbons (PAHs), toxic organic compounds, and heavy metals. The combination of high population density, meteorological conditions, and industrial productivity brings high levels of air pollution to the metropolitan area of El Paso, Texas, USA/ Ciudad Juarez, Chihuahua, Mexico, comprising the Paso del Norte air basin. A study conducted by scientists from the Research Triangle Park in North Carolina, analyzed sites adjacent to heavy-traffic highways in El Paso and elucidated higher UFP concentrations in comparison to previously published work exploring pollution and adverse health effects in the basin. UFPs can penetrate deep into the alveolar sacs of the lung, reaching distant alveolar sacs and inducing a series of immune responses that are detrimental to the body: evidence suggests that UFPs can also cross the alveolar-blood barrier and potentially endanger the body's immune response. The physical properties of UFPs and the dynamics of local atmospheric and topographical conditions indicate that emissions of nanosized carbonaceous aerosols could pose significant threats to biological tissues upon inhalation by local residents of the Paso del Norte. This study utilizes Black Carbon (BC) as a model for environmental UFPs and its effects on the immunological response. An in vitro approach is used to measure the ability of BC to promote cell death upon long-term exposure. Human epithelial lung cells (A549), human peripheral-blood monocytes (THP-1), murine macrophages (RAW264.7), and murine epithelial lung cells (LA-4) were treated with BC and assessed for metabolic activity after chronic exposure utilizing three distinct and independent cell viability assays. The cell viability

  8. 40 CFR 60.672 - Standard for particulate matter (PM).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... PROGRAMS (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES Standards of Performance for Nonmetallic Mineral Processing Plants § 60.672 Standard for particulate matter (PM). (a) Affected...

  9. Characterizing Aerosolized Particulate As Part Of A Nanoprocess Exposure Assessment

    SciTech Connect

    Jankovic, John Timothy; Ogle, Burton R; Zontek, Tracy L; Hollenbeck, Scott M

    2010-01-01

    The purpose of this effort was to propose important aerosol characterization parameters that should be gathered as part of a nanomaterial hazard assessment and to offer a methodology for applying that data to daily operations. This study documents different ways of characterizing nanoscale materials using an aerosol from a process simulation consisting of a vacuum cleaner motor operating inside an enclosure. The aerosol is composed of insoluble carbon particles plus environmental background constituents. The average air concentration is 2.76E+5 p/cm3. Size measurements of the aerosol indicate > 70% of the particulate is blade-like in shape, 50% of which have a height dimension 100 nm. In terms of an equivalent spherical diameter 0.8% of the particulate is 100 nm in size. The carbon blades are characterized as having a root-mean-square roughness of 75 nm, and average fractal dimension of 2.25. These measures: aerosol chemistry, solubility, shape and size, surface area, number concentration and size distribution are important parameters to collect for current exposure assessment and toxicology and epidemiology studies.

  10. Workshop on Aerosols and Particulates from Aircraft Gas Turbine Engines

    NASA Technical Reports Server (NTRS)

    Wey, Chown Chou (Compiler)

    1999-01-01

    In response to the National Research Council (NRC) recommendations, the Workshop on Aerosols and Particulates from Aircraft Gas Turbine Engines was organized by the NASA Lewis Research Center and held on July 29-30, 1997 at the Ohio Aerospace Institute in Cleveland, Ohio. The objective is to develop consensus among experts in the field of aerosols from gas turbine combustors and engines as to important issues and venues to be considered. Workshop participants' expertise included engine and aircraft design, combustion processes and kinetics, atmospheric science, fuels, and flight operations and instrumentation.

  11. Characterization of coarse particulate matter in school gyms.

    PubMed

    Braniš, Martin; Šafránek, Jiří

    2011-05-01

    We investigated the mass concentration, mineral composition and morphology of particles resuspended by children during scheduled physical education in urban, suburban and rural elementary school gyms in Prague (Czech Republic). Cascade impactors were deployed to sample the particulate matter. Two fractions of coarse particulate matter (PM(10-2.5) and PM(2.5-1.0)) were characterized by gravimetry, energy dispersive X-ray spectrometry and scanning electron microscopy. Two indicators of human activity, the number of exercising children and the number of physical education hours, were also recorded. Lower mass concentrations of coarse particulate matter were recorded outdoors (average PM(10-2.5) 4.1-7.4 μg m(-3) and PM(2.5-1.0) 2.0-3.3 μg m(-3)) than indoors (average PM(10-2.5) 13.6-26.7 μg m(-3) and PM(2.5-1.0) 3.7-7.4 μg m(-3)). The indoor concentrations of coarse aerosol were elevated during days with scheduled physical education with an average indoor-outdoor (I/O) ratio of 2.5-16.3 for the PM(10-2.5) and 1.4-4.8 for the PM(2.5-1.0) values. Under extreme conditions, the I/O ratios reached 180 (PM(10-2.5)) and 19.1 (PM(2.5-1.0)). The multiple regression analysis based on the number of students and outdoor coarse PM as independent variables showed that the main predictor of the indoor coarse PM concentrations is the number of students in the gym. The effect of outdoor coarse PM was weak and inconsistent. The regression models for the three schools explained 60-70% of the particular dataset variability. X-ray spectrometry revealed 6 main groups of minerals contributing to resuspended indoor dust. The most abundant particles were those of crustal origin composed of Si, Al, O and Ca. Scanning electron microscopy showed that, in addition to numerous inorganic particles, various types of fibers and particularly skin scales make up the main part of the resuspended dust in the gyms. In conclusion, school gyms were found to be indoor microenvironments with high

  12. Methods of analysis for complex organic aerosol mixtures from urban emission sources of particulate carbon

    SciTech Connect

    Mazurek, M.A. ); Hildemann, L.M. . Dept. of Civil Engineering); Cass, G.R.; Rogge, W.F. . Dept. of Environmental Engineering Science); Simoneit, B.R.T. . Coll. of Oceanography)

    1990-04-01

    Extractable organic compounds having between 6 to 40 carbon atoms comprise an important mass fraction of the fine particulate matter samples from major urban emission sources. Depending on the emission source type, this solvent-soluble fraction accounts for <20% to 100% of the total organic aerosol mass, as measured by quantitative high-resolution has chromatography (HRGC) with flame ionization detection. In addition to total extract quantitation, HRGC can be applied to further analyses of the mass distributions of elutable organics present in the complex aerosol extract mixtures, thus generating profiles that serve as fingerprints'' for the sources of interest. This HRGC analytical method is applied to emission source samples that contain between 7 to 12,000 {mu}g/filter organic carbon. It is shown to be a sensitive technique for analysis of carbonaceous aerosol extract mixtures having diverse mass loadings and species distributions. This study describes the analytical chemical methods that have been applied to: the construction of chemical mass balances based on the mass of fine organic aerosol emitted for major urban sources of particulate carbon; and the generation of discrete emission source chemical profiles derived from chromatographic characteristics of the organic aerosol components. 21 refs., 1 fig., 2 tabs.

  13. 40 CFR 52.1374 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Particulate matter. 52.1374 Section 52.1374 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) On July 8, 1997, the Governor of Montana submitted...

  14. 40 CFR 52.2429 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 5 2012-07-01 2012-07-01 false Control strategy: Particulate matter. 52.2429 Section 52.2429 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. Determination of Attainment. EPA has determined, as of January...

  15. 40 CFR 52.1131 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Particulate matter. 52.1131 Section 52.1131 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) Revisions to the following regulations submitted on March...

  16. 40 CFR 52.2429 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 5 2014-07-01 2014-07-01 false Control strategy: Particulate matter. 52.2429 Section 52.2429 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. Determination of Attainment. EPA has determined, as of January...

  17. 40 CFR 52.1025 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Particulate matter. 52.1025 Section 52.1025 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... strategy: Particulate matter. (a) The revisions to the control strategy resulting from the modification...

  18. 40 CFR 52.2526 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 5 2013-07-01 2013-07-01 false Control strategy: Particulate matter. 52.2526 Section 52.2526 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) EPA approves West Virginia's November 15, 1991 SIP submittal...

  19. 40 CFR 52.332 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 3 2013-07-01 2013-07-01 false Control strategy: Particulate matter. 52.332 Section 52.332 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR...: Particulate matter. (a) On April 9, 1992, the Governor of Colorado submitted the moderate PM-10...

  20. 40 CFR 52.1025 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Control strategy: Particulate matter. 52.1025 Section 52.1025 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... strategy: Particulate matter. (a) The revisions to the control strategy resulting from the modification...

  1. 40 CFR 52.1341 - Control strategy: particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: particulate matter. 52.1341 Section 52.1341 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: particulate matter. Determination of Attainment. EPA has determined, as of May 23,...

  2. 40 CFR 52.332 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 3 2014-07-01 2014-07-01 false Control strategy: Particulate matter. 52.332 Section 52.332 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR...: Particulate matter. (a) On April 9, 1992, the Governor of Colorado submitted the moderate PM-10...

  3. 40 CFR 52.2429 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 5 2013-07-01 2013-07-01 false Control strategy: Particulate matter. 52.2429 Section 52.2429 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. Determination of Attainment. EPA has determined, as of January...

  4. 40 CFR 52.2526 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Particulate matter. 52.2526 Section 52.2526 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) EPA approves West Virginia's November 15, 1991 SIP submittal...

  5. 40 CFR 52.477 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 3 2014-07-01 2014-07-01 false Control strategy: Particulate matter. 52.477 Section 52.477 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. Determination of Attainment. EPA has determined, as of January...

  6. 40 CFR 52.1025 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Particulate matter. 52.1025 Section 52.1025 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... strategy: Particulate matter. (a) The revisions to the control strategy resulting from the modification...

  7. 40 CFR 52.1025 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Particulate matter. 52.1025 Section 52.1025 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... strategy: Particulate matter. (a) The revisions to the control strategy resulting from the modification...

  8. 40 CFR 52.1374 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Particulate matter. 52.1374 Section 52.1374 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) On July 8, 1997, the Governor of Montana submitted...

  9. 40 CFR 52.1374 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Particulate matter. 52.1374 Section 52.1374 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) On July 8, 1997, the Governor of Montana submitted...

  10. 40 CFR 52.1131 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Particulate matter. 52.1131 Section 52.1131 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) Revisions to the following regulations submitted on March...

  11. Method for removing particulate matter from a gas stream

    DOEpatents

    Postma, Arlin K.

    1984-01-01

    Particulate matter is removed from a stream of pressurized gas by directing the stream of gas upwardly through a bed of porous material, the porous bed being held in an open ended container and at least partially submerged in liquid. The passage of the gas through the porous bed sets up a circulation in the liquid which cleans the particulate matter from the bed.

  12. 40 CFR 52.427 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 3 2012-07-01 2012-07-01 false Control strategy: Particulate matter. 52.427 Section 52.427 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR...: Particulate matter. Determination of attainment. EPA has determined, as of May 16, 2012, that based on 2007...

  13. 40 CFR 52.1025 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 4 2014-07-01 2014-07-01 false Control strategy: Particulate matter. 52.1025 Section 52.1025 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... strategy: Particulate matter. (a) The revisions to the control strategy resulting from the modification...

  14. 40 CFR 52.2526 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Particulate matter. 52.2526 Section 52.2526 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) EPA approves West Virginia's November 15, 1991 SIP submittal...

  15. 40 CFR 52.477 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 3 2012-07-01 2012-07-01 false Control strategy: Particulate matter. 52.477 Section 52.477 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. Determination of Attainment. EPA has determined, as of January...

  16. 40 CFR 52.1081 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Particulate matter. 52.1081 Section 52.1081 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) Determination of Attainment. EPA has determined, as of...

  17. 40 CFR 52.332 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 3 2012-07-01 2012-07-01 false Control strategy: Particulate matter. 52.332 Section 52.332 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR...: Particulate matter. (a) On April 9, 1992, the Governor of Colorado submitted the moderate PM-10...

  18. 40 CFR 52.1341 - Control strategy: particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: particulate matter. 52.1341 Section 52.1341 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: particulate matter. Determination of Attainment. EPA has determined, as of May 23,...

  19. 40 CFR 52.2526 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 5 2014-07-01 2014-07-01 false Control strategy: Particulate matter. 52.2526 Section 52.2526 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) EPA approves West Virginia's November 15, 1991 SIP submittal...

  20. 40 CFR 52.1131 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Control strategy: Particulate matter. 52.1131 Section 52.1131 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) Revisions to the following regulations submitted on March...

  1. 40 CFR 52.2429 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Particulate matter. 52.2429 Section 52.2429 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. Determination of Attainment. EPA has determined, as of January...

  2. 40 CFR 52.1081 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Particulate matter. 52.1081 Section 52.1081 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) Determination of Attainment. EPA has determined, as of...

  3. 40 CFR 52.332 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 3 2011-07-01 2011-07-01 false Control strategy: Particulate matter. 52.332 Section 52.332 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR...: Particulate matter. (a) On April 9, 1992, the Governor of Colorado submitted the moderate PM-10...

  4. 40 CFR 52.1081 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Particulate matter. 52.1081 Section 52.1081 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) Determination of Attainment. EPA has determined, as of...

  5. 40 CFR 52.477 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 3 2011-07-01 2011-07-01 false Control strategy: Particulate matter. 52.477 Section 52.477 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. Determination of Attainment. EPA has determined, as of January...

  6. 40 CFR 52.1374 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Control strategy: Particulate matter. 52.1374 Section 52.1374 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) On July 8, 1997, the Governor of Montana submitted...

  7. 40 CFR 52.2429 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Particulate matter. 52.2429 Section 52.2429 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. Determination of Attainment. EPA has determined, as of January...

  8. 40 CFR 52.2526 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 5 2012-07-01 2012-07-01 false Control strategy: Particulate matter. 52.2526 Section 52.2526 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) EPA approves West Virginia's November 15, 1991 SIP submittal...

  9. 40 CFR 52.1131 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Particulate matter. 52.1131 Section 52.1131 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) Revisions to the following regulations submitted on March...

  10. 40 CFR 52.477 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 3 2013-07-01 2013-07-01 false Control strategy: Particulate matter. 52.477 Section 52.477 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. Determination of Attainment. EPA has determined, as of January...

  11. 40 CFR 52.1081 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 4 2014-07-01 2014-07-01 false Control strategy: Particulate matter. 52.1081 Section 52.1081 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. (a) Determination of Attainment. EPA has determined, as of...

  12. 40 CFR 52.477 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 3 2010-07-01 2010-07-01 false Control strategy: Particulate matter. 52.477 Section 52.477 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy: Particulate matter. Determination of Attainment. EPA has determined, as of January...

  13. 2009 Final Report: Integrated Science Assessment for Particulate Matter

    EPA Science Inventory

    EPA released the final Integrated Science Assessment (ISA) for Particulate Matter (PM). This is EPA’s latest evaluation of the scientific literature on the potential human health and welfare effects associated with ambient exposures to particulate matter (PM). The develop...

  14. MODELING ENVIRONMENTAL EXPOSURES TO PARTICULATE MATTER AND PESTICIDES

    EPA Science Inventory

    This presentation describes initial results from on-going research at EPA on modeling human exposures to particulate matter and residential pesticides. A first generation probabilistic population exposure model for Particulate Matter (PM), specifically for predicting PM1o and P...

  15. 40 CFR 60.532 - Standards for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standards for particulate matter. 60.532 Section 60.532 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS... Wood Heaters § 60.532 Standards for particulate matter. Unless exempted under § 60.530, each...

  16. 40 CFR 60.532 - Standards for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standards for particulate matter. 60.532 Section 60.532 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS... Wood Heaters § 60.532 Standards for particulate matter. Unless exempted under § 60.530, each...

  17. 40 CFR 60.532 - Standards for particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standards for particulate matter. 60.532 Section 60.532 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS... Wood Heaters § 60.532 Standards for particulate matter. Unless exempted under § 60.530, each...

  18. 40 CFR 60.532 - Standards for particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 7 2012-07-01 2012-07-01 false Standards for particulate matter. 60.532 Section 60.532 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS... Wood Heaters § 60.532 Standards for particulate matter. Unless exempted under § 60.530, each...

  19. 40 CFR 60.532 - Standards for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standards for particulate matter. 60.532 Section 60.532 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS... Wood Heaters § 60.532 Standards for particulate matter. Unless exempted under § 60.530, each...

  20. 40 CFR 60.282 - Standard for particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... § 60.282 Standard for particulate matter. (a) On and after the date on which the performance test... particulate matter in excess of 0.1 g/kg black liquor solids (dry weight) . (3) From any lime kiln any...

  1. Lability of Secondary Organic Particulate Matter

    SciTech Connect

    Liu, Pengfei; Li, Yong Jie; Wang, Yan; Giles, Mary K.; Zaveri, Rahul A.; Bertram, Allan K.; Martin, Scot T.

    2016-10-24

    Accurate simulations of the consenctrations of atmospheric organic particulate matter (PM) are needed for predicting energy flow in the Earth’s climate system. In the past, simulations of organic PM widely assume equilibrium partitioning of semivolatile organic compounds (SVOCs) between the PM and surrounding vapor. Herein, we test this assumption by measuring evaporation rates and associated vapor mass concentration of organic films representative of atmospheric PM. For films representing anthropogenic PM, evaporation rates and vapor mass concentrations increased above a threshold relative humidity (RH), indicating equilibrium partitioning above a transition RH but not below. In contrast for films representing biogenic PM, no threshold was observed, indicating equilibrium partitioning at all RHs. The results suggest that the mass lability of atmospheric organic PM can differ in consequential ways among Earth’s natural biomes, polluted regions, and regions of land-use change, and these differences need to be considered when simulating atmospheric organic PM.

  2. GIST-PM-Asia v1: development of a numerical system to improve particulate matter forecasts in South Korea using geostationary satellite-retrieved aerosol optical data over Northeast Asia

    NASA Astrophysics Data System (ADS)

    Lee, S.; Song, C. H.; Park, R. S.; Park, M. E.; Han, K. M.; Kim, J.; Choi, M.; Ghim, Y. S.; Woo, J.-H.

    2016-01-01

    To improve short-term particulate matter (PM) forecasts in South Korea, the initial distribution of PM composition, particularly over the upwind regions, is primarily important. To prepare the initial PM composition, the aerosol optical depth (AOD) data retrieved from a geostationary equatorial orbit (GEO) satellite sensor, GOCI (Geostationary Ocean Color Imager) which covers a part of Northeast Asia (113-146° E; 25-47° N), were used. Although GOCI can provide a higher number of AOD data in a semicontinuous manner than low Earth orbit (LEO) satellite sensors, it still has a serious limitation in that the AOD data are not available at cloud pixels and over high-reflectance areas, such as desert and snow-covered regions. To overcome this limitation, a spatiotemporal-kriging (STK) method was used to better prepare the initial AOD distributions that were converted into the PM composition over Northeast Asia. One of the largest advantages in using the STK method in this study is that more observed AOD data can be used to prepare the best initial AOD fields compared with other methods that use single frame of observation data around the time of initialization. It is demonstrated in this study that the short-term PM forecast system developed with the application of the STK method can greatly improve PM10 predictions in the Seoul metropolitan area (SMA) when evaluated with ground-based observations. For example, errors and biases of PM10 predictions decreased by ˜ 60 and ˜ 70 %, respectively, during the first 6 h of short-term PM forecasting, compared with those without the initial PM composition. In addition, the influences of several factors on the performances of the short-term PM forecast were explored in this study. The influences of the choices of the control variables on the PM chemical composition were also investigated with the composition data measured via PILS-IC (particle-into-liquid sampler coupled with ion chromatography) and low air-volume sample

  3. EDITORIAL: Global impacts of particulate matter air pollution

    NASA Astrophysics Data System (ADS)

    Bell, Michelle L.; Holloway, Tracey

    2007-10-01

    Even in well-studied, data-rich regions of the United States and Europe, understanding ambient particulate matter (PM, aka aerosols) remains a challenge. Atmospheric aerosols exhibit chemical heterogeneity, spatial and seasonal variability, and result in a wide range of health impacts (mortality, respiratory disease, cardiovascular disease, eye irritation, and others). In addition, aerosols play an important role in climate, exerting warming effects (black carbon), cooling effects (sulfate and organic carbon), and affecting precipitation and cloud cover. Characterizing the emission sources, concentrations, transport patterns, and impacts is particularly difficult in developing countries, where data are scarce, emissions are high, and health impacts are often severe. We are pleased to present this focus issue of Environmental Research Letters (ERL) devoted to the study of PM on an international scale. Our authors are leading researchers who each bring cross-cutting analysis to this critical health and environmental issue. Collectively, the research presented here contributes to our understanding of PM sources, processes, and impacts, while highlighting key steps forward. In this issue, Zhang et al examine the size distribution and composition of emitted anthropogenic PM in China, finding that the characteristics of primary aerosol emissions differ significantly between industrialized and developing regions in China. Concentration measurements of PM, like detailed emissions inventories, are rare in the developing world. van Vliet and Kinney analyze fine particles in Nairobi based on monitoring data for PM2.5 and black carbon. Using measurements from multiple locations of differing proximity to roadways, the authors evaluate traffic-source contributions to PM exposure. The impact of emission location and exposed population are also evaluated by Liu and Mauzerall, but on a continent-to-continent scale. The authors quantify the connection between SO2 emissions and

  4. 75 FR 55711 - Federal Implementation Plans To Reduce Interstate Transport of Fine Particulate Matter and Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-09-14

    ... Interstate Transport of Fine Particulate Matter and Ozone; Correction AGENCY: Environmental Protection Agency..., Nitrogen oxides, Ozone, Particulate matter, Regional haze, Reporting and recordkeeping requirements,...

  5. Factors Controlling Liquid Particulate Matter in Amazonia

    NASA Astrophysics Data System (ADS)

    Bateman, A. P.; Gong, Z.; de Sá, S. S.; Wernis, R. A.; Yee, L.; Isaacman-VanWertz, G. A.; Goldstein, A. H.; Castillo, P.; Sedlacek, A. J., III; Palm, B. B.; Campuzano-Jost, P.; Day, D. A.; Hu, W.; Jimenez, J. L.; Alexander, L.; Manzi, A. O.; Souza, R. A. F. D.; Artaxo, P.; Martin, S. T.

    2015-12-01

    The hygroscopic response of particulate matter (PM) during GoAmazon 2014/5 was investigated through the use of particle rebound (or lack thereof) during impaction. The hygroscopic response was measured online and in real-time using a custom designed impaction apparatus. The impaction apparatus was calibrated with respect to particle viscosity indicating a liquid state (viscosity <102 Pa s) for complete adherence (no particle rebound). By varying the PM water content and observing particle rebound as a function of RH (up to 98%), the hygroscopic response and phase state of the PM under investigation was determined. The hygroscopic response curves were categorized according to the rebound fraction at high RH (80 - 98%) bounded by two extremes. 1) Time periods that resemble pure SOM generated under controlled chamber conditions, where no particle rebound is observed above 80% RH. 2) Time periods that a large fraction (10 - 40%) of particles rebound at RH values >95%, an indication of hydrophobic particles. The role of anthropogenic and biogenic factors in controlling the hygroscopic response of PM in Amazonia is investigated through meteorological conditions and particle chemical composition.

  6. Source apportionment of particulate matter in a large city of southeastern Po Valley (Bologna, Italy).

    PubMed

    Tositti, L; Brattich, E; Masiol, M; Baldacci, D; Ceccato, D; Parmeggiani, S; Stracquadanio, M; Zappoli, S

    2014-01-01

    This study reports the results of an experimental research project carried out in Bologna, a midsize town in central Po valley, with the aim at characterizing local aerosol chemistry and tracking the main source emissions of airborne particulate matter. Chemical speciation based upon ions, trace elements, and carbonaceous matter is discussed on the basis of seasonal variation and enrichment factors. For the first time, source apportionment was achieved at this location using two widely used receptor models (principal component analysis/multi-linear regression analysis (PCA/MLRA) and positive matrix factorization (PMF)). Four main aerosol sources were identified by PCA/MLRA and interpreted as: resuspended particulate and a pseudo-marine factor (winter street management), both related to the coarse fraction, plus mixed combustions and secondary aerosol largely associated to traffic and long-lived species typical of the fine fraction. The PMF model resolved six main aerosol sources, interpreted as: mineral dust, road dust, traffic, secondary aerosol, biomass burning and again a pseudo-marine factor. Source apportionment results from both models are in good agreement providing a 30 and a 33% by weight respectively for PCA-MLRA and PMF for the coarse fraction and 70% (PCA-MLRA) and 67% (PMF) for the fine fraction. The episodic influence of Saharan dust transport on PM10 exceedances in Bologna was identified and discussed in term of meteorological framework, composition, and quantitative contribution.

  7. 75 FR 17865 - Approval and Promulgation of Air Quality Implementation Plans; Wisconsin; Particulate Matter...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-04-08

    ...; Particulate Matter Standards AGENCY: Environmental Protection Agency (EPA). ACTION: Direct final rule. SUMMARY... updates were made to the particulate matter standards by adding fine particulate standards and revoking the state's course particulate standards. EPA revised its particulate matter standards in October...

  8. 76 FR 5270 - Approval and Promulgation of Air Quality Implementation Plans; Wisconsin; Particulate Matter...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-01-31

    ... particulates can cause heart and lung disease. Particulate matter also aggravates asthma. Airborne particulate... more for fine particulates. WPC states that it would be difficult for sources to limit PM 2.5...

  9. Setting and Reviewing Standards to Control Particulate Matter (PM) Pollution

    EPA Pesticide Factsheets

    The Clean Air Act requires EPA to set national air quality standards for particulate matter, and to periodically review the standards to ensure that they provide adequate health and environmental protection, updating those standards as necessary.

  10. Monitoring by Control Technique - Wet Scrubber For Particulate Matter

    EPA Pesticide Factsheets

    Stationary source emissions monitoring is required to demonstrate that a source is meeting the requirements in Federal or state rules. This page is about Wet Scrubber For Particulate Matter controls used to reduce pollutant emissions.

  11. Canada-United States Transboundary Particulate Matter Science Assessment

    EPA Pesticide Factsheets

    This 2004 document summarizes the findings of the Canada-U.S. subcommittee on Scientific Cooperation concerning the transboundary transport of particulate matter (PM) and PM precursors between the two countries.

  12. COMPARISON OF METHODS FOR MEASURING CONCENTRATIONS OF SEMIVOLATILE PARTICULATE MATTER

    EPA Science Inventory

    The paper gives results of a comparison of methods for measuring concentrations of semivolatile particulate matter (PM) from indoor-environment, small, combustion sources. Particle concentration measurements were compared for methods using filters and a small electrostatic precip...

  13. ULTRAFINE PARTICULATE MATTER EXPOSURE AUGMENTS ISCHEMIA REPERFUSION INJURY IN MICE

    EPA Science Inventory

    Epidemiological studies have linked ambient particulate matter (PM) levels to an increased incidence of adverse cardiovascular events. Yet little is definitively known about the mechanisms accounting for the cardiovascular events associated with PM-exposure. The goal of this stud...

  14. ULTRAFINE PARTICULATE MATTER EXPOSURE AUGMENTS ISCHEMIA REPERFUSION INJURY IN MICE

    EPA Science Inventory

    Epidemiological studies have linked ambient particulate matter (PM) levels to an increased incidence of adverse cardiovascular events. Yet little is definitively known about the mechanisms accounting for the cardiovascular events associated with PM exposure. The goal of thi...

  15. PARTICULATE MATTER CONCENTRATIONS IN NON-RESIDENTIAL MICROENVIRONMENTS

    EPA Science Inventory

    Exposures to airborne particulate matter (PM) have long been associated with increases in both acute and chronic human health effects. Traditionally, research and regulations have focused on outdoor air pollution. However, human activity pattern studies show that people are ind...

  16. Canada-United States Transboundary Particulate Matter Science Assessment 2013

    EPA Pesticide Factsheets

    This 2013 document summarizes the findings of the Canada-U.S. subcommittee on Scientific Cooperation concerning the transboundary transport of particulate matter (PM) and PM precursors between the two countries.

  17. 40 CFR 266.105 - Standards to control particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... HAZARDOUS WASTE MANAGEMENT FACILITIES Hazardous Waste Burned in Boilers and Industrial Furnaces § 266.105 Standards to control particulate matter. (a) A boiler or industrial furnace burning hazardous waste may...

  18. 40 CFR 266.105 - Standards to control particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... HAZARDOUS WASTE MANAGEMENT FACILITIES Hazardous Waste Burned in Boilers and Industrial Furnaces § 266.105 Standards to control particulate matter. (a) A boiler or industrial furnace burning hazardous waste may...

  19. 40 CFR 266.105 - Standards to control particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... HAZARDOUS WASTE MANAGEMENT FACILITIES Hazardous Waste Burned in Boilers and Industrial Furnaces § 266.105 Standards to control particulate matter. (a) A boiler or industrial furnace burning hazardous waste may...

  20. 40 CFR 266.105 - Standards to control particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... HAZARDOUS WASTE MANAGEMENT FACILITIES Hazardous Waste Burned in Boilers and Industrial Furnaces § 266.105 Standards to control particulate matter. (a) A boiler or industrial furnace burning hazardous waste may...

  1. AMBIENT PARTICULATE MATTER DECREASED IN HUMAN ALVEOLAR MACHROPHAGE CYTOKINE RELEASE

    EPA Science Inventory

    Human exposure to ambient airborne particulate matter (PM) is associated with cardiopulmonary mortality and morbidity, including increased hospitalizations for lung infection. Normal lung immune responses to bacterial infection include alveolar macrophage cytokine production and...

  2. Effect of ambient particulate matter expousre on hemostasis

    EPA Science Inventory

    Epidemiological studies have linked levels of particulate matter (PM) in ambient air to cardiovascular mortality and hospitalizations for myocardial infarction (MI) and stroke. Thrombus formation plays a primary role in potentiating acute cardiovascular events, and this study was...

  3. 75 FR 30710 - Approval and Promulgation of Air Quality Implementation Plans; Wisconsin; Particulate Matter...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-06-02

    ... Implementation Plans; Wisconsin; Particulate Matter Standards; Withdrawal of Direct Final Rule AGENCY... matter standards by adding fine particulate standards and revoking the state's course particulate standards. The State of Wisconsin submitted this revision as a modification to the State Implementation...

  4. Bioaccessibility of palladium and platinum in urban aerosol particulates

    NASA Astrophysics Data System (ADS)

    Puls, Christoph; Limbeck, Andreas; Hann, Stephan

    2012-08-01

    To evaluate potential health hazards caused by environmental Platinum Group Elements (PGEs), bioaccessibility of the metals in question needs to be assessed. To gain appropriate data, airborne particulate matter samples of different size fractions (total suspended particles as well as PM10 and PM2.5) were taken in downtown Vienna, an urban site primarily polluted by traffic. Total PGE concentrations in these samples were in the low picogram per cubic meter range, as determined by ID-ICP-MS after microwave digestion. For elimination of elements interfering with the accurate quantification, the digested samples were subjected to a cleaning procedure involving cation exchange. For determination of the bioaccessible fraction, it was assumed that inhaled particles are removed from the respiratory system by mucociliary clearance and subsequently ingested. Accordingly, the solubility of PGE in synthetic gastric juice was investigated by batch extraction of particulate matter samples followed by microwave assisted UV-digestion, cation exchange cleanup and ID-ICP-MS. The acquired data was used to calculate the bioaccessible fraction of Pd and Pt in airborne particulate matter. Average GIT-extractable fractions for Pd and Pt in TSP were 41% and 27%, in PM10 34% and 26%, respectively, thus exceeding previously determined values for bioaccessibility of PGE from ground catalyst materials by up to an order of magnitude.

  5. Air Quality Criteria for Particulate Matter.

    ERIC Educational Resources Information Center

    National Air Pollution Control Administration (DHEW), Washington, DC.

    To assist states in developing air quality standards, this book offers a review of literature related to atmospheric particulates and the development of criteria for air quality. It not only summarizes the current scientific knowledge of particulate air pollution, but points up the major deficiencies in that knowledge and the need for further…

  6. Source Apportionment of Ambient Fine Particulate Matter in Dearborn, Michigan, using Hourly Resolved PM Chemical Composition Data

    EPA Science Inventory

    High time-resolution aerosol sampling was conducted for one month during July–August 2007 in Dearborn, MI, a non-attainment area for fine particulate matter (PM2.5) National Ambient Air Quality Standards (NAAQS). Measurements of more than 30 PM2.5 species were made using a suite o...

  7. EVALUATION OF METHODS FOR THE DETERMINATION OF DIESEL-GENERATED FINE PARTICULATE MATTER: PHYSICAL CHARACTERIZATION OF RESULTS

    EPA Science Inventory

    A multi-phase instrument comparison study was conducted on two different diesel engines on a dynamometer to compare commonly used particulate matter (PM) measurement techniques while sampling the same diesel exhaust aerosol and to evaluate inter- and intra-method variability. In...

  8. A comprehensive particulate matter monitoring system and dosimetry-based ambient particulate matter standards.

    PubMed

    Zeng, Yousheng

    2006-04-01

    A numerical particulate matter (PM) measurement model is developed to characterize and evaluate PM sampling methods. Simulations are conducted using the model to evaluate currently widely used PM samplers, including Federal Reference Method (FRM) samplers. The simulations show that current PM samplers are very vulnerable to both changes in measurement target (i.e., natural variability of particle size distribution) and the sampler's design, manufacturing, and operating conditions, potentially resulting in significant errors in the monitoring data. The numerical model is used in conjunction with two types of commercially available PM monitoring devices to form a Comprehensive Particulate Matter Monitoring System (CPMMS). The first type of device can be any mass-based PM monitor with a well-defined sampling efficiency curve. The second type of device is one capable of measuring particle size distribution with a reasonably good relative accuracy between size categories but not necessarily accurate in measuring absolute mass concentrations. This study shows that CPMMS can produce much higher quality PM monitoring data than the current PM samplers under the same conditions. In addition, unlike past and current PM monitoring data such as total suspended particulates, coarse PM (PM10), fine PM (PM2.5), etc., the CPMMS monitoring data will survive changes in PM regulatory definition. A new concept, dosimetry-based PM metrics and standards, is proposed to define ambient PM level based on the deposition fraction of particles in the human respiratory tract. The dosimetry-based PM metrics is more meaningful because it correlates the ambient PM level with the portion that can be deposited in the respiratory tract without an arbitrary cutoff particle diameter. CPMMS makes dosimetry-based PM metrics and standards feasible.

  9. Characterization of coarse particulate matter in school gyms

    SciTech Connect

    Branis, Martin; Safranek, Jiri

    2011-05-15

    We investigated the mass concentration, mineral composition and morphology of particles resuspended by children during scheduled physical education in urban, suburban and rural elementary school gyms in Prague (Czech Republic). Cascade impactors were deployed to sample the particulate matter. Two fractions of coarse particulate matter (PM{sub 10-2.5} and PM{sub 2.5-1.0}) were characterized by gravimetry, energy dispersive X-ray spectrometry and scanning electron microscopy. Two indicators of human activity, the number of exercising children and the number of physical education hours, were also recorded. Lower mass concentrations of coarse particulate matter were recorded outdoors (average PM{sub 10-2.5} 4.1-7.4 {mu}g m{sup -3} and PM{sub 2.5-1.0} 2.0-3.3 {mu}g m{sup -3}) than indoors (average PM{sub 10-2.5} 13.6-26.7 {mu}g m{sup -3} and PM{sub 2.5-1.0} 3.7-7.4 {mu}g m{sup -3}). The indoor concentrations of coarse aerosol were elevated during days with scheduled physical education with an average indoor-outdoor (I/O) ratio of 2.5-16.3 for the PM{sub 10-2.5} and 1.4-4.8 for the PM{sub 2.5-1.0} values. Under extreme conditions, the I/O ratios reached 180 (PM{sub 10-2.5}) and 19.1 (PM{sub 2.5-1.0}). The multiple regression analysis based on the number of students and outdoor coarse PM as independent variables showed that the main predictor of the indoor coarse PM concentrations is the number of students in the gym. The effect of outdoor coarse PM was weak and inconsistent. The regression models for the three schools explained 60-70% of the particular dataset variability. X-ray spectrometry revealed 6 main groups of minerals contributing to resuspended indoor dust. The most abundant particles were those of crustal origin composed of Si, Al, O and Ca. Scanning electron microscopy showed that, in addition to numerous inorganic particles, various types of fibers and particularly skin scales make up the main part of the resuspended dust in the gyms. In conclusion, school

  10. Sources and Processes Affecting Particulate Matter Pollution over North China

    NASA Astrophysics Data System (ADS)

    Zhang, L.; Shao, J.; Lu, X.; Zhao, Y.; Gong, S.; Henze, D. K.

    2015-12-01

    Severe fine particulate matter (PM2.5) pollution over North China has received broad attention worldwide in recent years. Better understanding the sources and processes controlling pollution over this region is of great importance with urgent implications for air quality policy. We will present a four-dimensional variational (4D-Var) data assimilation system using the GEOS-Chem chemical transport model and its adjoint model at 0.25° × 0.3125° horizontal resolution, and apply it to analyze the factors affecting PM2.5 concentrations over North China. Hourly surface observations of PM2.5 and sulfur dioxide (SO2) from the China National Environmental Monitoring Center (CNEMC) can be assimilated into the model to evaluate and constrain aerosol (primary and precursors) emissions. Application of the data assimilation system to the APEC period (the Asia-Pacific Economic Cooperation summit; 5-11 November 2014) shows that 46% of the PM2.5 pollution reduction during APEC ("The APEC Blue") can be attributed to meteorology conditions and the rest 54% to emission reductions due to strict emission controls. Ammonia emissions are shown to significantly contribute to PM2.5 over North China in the fall. By converting sulfuric acid and nitric acid to longer-lived ammonium sulfate and ammonium nitrate aerosols, ammonia plays an important role in promoting their regional transport influences. We will also discuss the pathways and mechanisms of external long-range transport influences to the PM2.5 pollution over North China.

  11. Structure analysis and size distribution of particulate matter from candles and kerosene combustion in burning chamber

    NASA Astrophysics Data System (ADS)

    Baitimirova, M.; Osite, A.; Katkevics, J.; Viksna, A.

    2012-08-01

    Burning of candles generates particulate matter of fine dimensions that produces poor indoor air quality, so it may cause harmful impact on human health. In this study solid aerosol particles of burning of candles of different composition and kerosene combustion were collected in a closed laboratory system. Present work describes particulate matter collection for structure analysis and the relationship between source and size distribution of particulate matter. The formation mechanism of particulate matter and their tendency to agglomerate also are described. Particles obtained from kerosene combustion have normal size distribution. Whereas, particles generated from the burning of stearin candles have distribution shifted towards finer particle size range. If an additive of stearin to paraffin candle is used, particle size distribution is also observed in range of towards finer particles. A tendency to form agglomerates in a short time is observed in case of particles obtained from kerosene combustion, while in case of particles obtained from burning of candles of different composition such a tendency is not observed. Particles from candles and kerosene combustion are Aitken and accumulation mode particles

  12. Particulate PAH emissions from residential biomass combustion: time-resolved analysis with aerosol mass spectrometry.

    PubMed

    Eriksson, A C; Nordin, E Z; Nyström, R; Pettersson, E; Swietlicki, E; Bergvall, C; Westerholm, R; Boman, C; Pagels, J H

    2014-06-17

    Time-resolved emissions of particulate polycyclic aromatic hydrocarbons (PAHs) and total organic particulate matter (OA) from a wood log stove and an adjusted pellet stove were investigated with high-resolution time-of-flight aerosol mass spectrometry (AMS). The highest OA emissions were found during the addition of log wood on glowing embers, that is, slow burning pyrolysis conditions. These emissions contained about 1% PAHs (of OA). The highest PAH emissions were found during fast burning under hot air starved combustion conditions, in both stoves. In the latter case, PAHs contributed up to 40% of OA, likely due to thermal degradation of other condensable species. The distribution of PAHs was also shifted toward larger molecules in these emissions. AMS signals attributed to PAHs were found at molecular weights up to 600 Da. The vacuum aerodynamic size distribution was found to be bimodal with a smaller mode (Dva ∼ 200 nm) dominating under hot air starved combustion and a larger sized mode dominating under slow burning pyrolysis (Dva ∼ 600 nm). Simultaneous reduction of PAHs, OA and total particulate matter from residential biomass combustion may prove to be a challenge for environmental legislation efforts as these classes of emissions are elevated at different combustion conditions.

  13. Driver exposure to particulate matter in Bangkok.

    PubMed

    Jinsart, W; Kaewmanee, C; Inoue, M; Hara, K; Hasegawa, S; Karita, K; Tamura, K; Yano, E

    2012-01-01

    The aims of this study were to determine the particulate matter with aerodynamic diameters > or = 2.5 microm (PM2.5) and 2.5-10 microm (PM10-2.5) exposure levels of drivers and to analyze the proportion of elemental carbon (EC) and organic carbon (OC) in PM2.5 in Bangkok, Thailand. Four bus routes were selected. Measurements were conducted over 10 days in August (rainy season) 2008 and 8 days in January (dry season) 2009. The mean PM2.5 exposure level of the Tuk-tuk drivers was 86 microg/m3 in August and 198 microg/m3 in January. The mean for the non-air-conditioned bus drivers was 63 microg/m3 in August and 125 microg/m3 in January. The PM2.5 and PM10-2.5 exposure levels of the drivers in January were approximately twice as high as those in August. The proportion of total carbon (TC) in PM2.5 to the PM2.5 level in August (0.97 +/- 0.28 microg/m3) was higher than in January (0.65 +/- 0.13 microg/m3). The proportion of OC in the TC of the PM2.5 in August (0.51 +/- 0.08 microg/m3) was similar to that in January (0.65 +/- 0.07 microg/m3). The TC exposure by PM25 in January (81 +/- 30 microg/m3) remained higher than in August (56-21 microg/m3). The mean level of OC in the PM2.5 was 29 +/- 13 microg/m3 in August and 50 +/- 24 microg/m3 in January. In conclusion, the PM exposure level in Bangkok drivers was higher than that in the general environment, which was already high, and it varied with the seasons and vehicle type. This study also demonstrated that the major component of the PM was carbon, likely derived from vehicles.

  14. [Light absorption by suspended particulate matter in Chagan Lake, Jilin].

    PubMed

    Wang, Yuan-Dong; Liu, Dian-Wei; Song, Kai-Shan; Zhang, Bai; Wang, Zong-Ming; Jiang, Guang-Ji; Tang, Xu-Guang; Lei, Xiao-Chun; Wu, Yan-Qing

    2011-01-01

    Spectral characteristics and the magnitudes of light absorption by suspended particulate matter were determined by spectrophotometry in this optically complex Lake Chagan waters for the purpose of surveying the natural variability of the absorption coefficients to parameterize the bio-optical models for converting satellite or in-situ water reflectance signatures into water quality information. Experiments were carried out on seasonal frozen Lake Chagan, one representative inland case-2 water body in Northeast of China. Particulate absorption properties analyzed using the field data on July 15th and October 12th 2009 were measured using the quantitative filter technique to produce absorption spectra containing several fractions that could be attributed to two main optical active constituents (OACs) phytoplankton pigments and non-algal particulates (mineral sediments, and organic detritus). Results suggested that the suspended particulate matter (SPM) concentration was higher while phytoplankton biomass (chlorophyll-a concentration) was lower in July and that in October. The spectral shape of total suspended particulate matter resembled that of non-algal particulates which contributed greater than phytoplankton in total particulate absorption during both periods. An obvious absorption peak occurring at around 440 nm exhibited an increase in phytoplankton contribution in October. Non-algal particulate absorption at 440 nm (a(NAP) (440)) had better correlation with total suspended particulate matter concentration than that with chlorophyll-a over the two periods. Light absorption by phytoplankton pigments in the Chagan lake region was generally lower than that of non-algal components. Chl. a dominating phytoplankton pigment composition functioned exponentially with its absorption coefficients at 440 and 675 nm specifically, the average values of which in July were 0.146 8 m2 x mg(-1) and 0.050 3 respectively while in October they were 0.153 3 and 0.013 2 m2 x mg(-1

  15. Vehicular emissions of organic particulate matter in Sao Paulo, Brazil

    NASA Astrophysics Data System (ADS)

    Oyama, B. S.; Andrade, M. F.; Herckes, P.; Dusek, U.; Röckmann, T.; Holzinger, R.

    2015-12-01

    Vehicular emissions have a strong impact on air pollution in big cities. Many factors affect these emissions: type of vehicle, type of fuel, cruising velocity, and brake use. This study focused on emissions of organic compounds by Light (LDV) and Heavy (HDV) duty vehicle exhaust. The study was performed in the city of Sao Paulo, Brazil, where vehicles run on different fuels: gasoline with 25 % ethanol (called gasohol), hydrated ethanol, and diesel (with 5 % of biodiesel). The vehicular emissions are an important source of pollutants and the principal contribution to fine particulate matter (smaller than 2.5 μm, PM2.5) in Sao Paulo. The experiments were performed in two tunnels: Janio Quadros (TJQ) where 99 % of the vehicles are LDV, and Rodoanel Mario Covas (TRA) where up to 30 % of the fleet was HDV. The PM2.5 samples were collected on quartz filters in May and July 2011 at TJQ and TRA, respectively, using two samplers operating in parallel. The samples were analyzed by Thermal-Desorption Proton-Transfer-Reaction Mass-Spectrometry (TD-PTR-MS), and by Thermal-Optical Transmittance (TOT). The organic aerosol (OA) desorbed at TD-PTR-MS represented around 30 % of the OA estimated by the TOT method, mainly due to the different desorption temperatures, with a maximum of 870 and 350 °C for TOT and TD-PTR-MS, respectively. Average emission factors (EF) organic aerosol (OA) and organic carbon (OC) were calculated for HDV and LDV fleet. We found that HDV emitted more OA and OC than LDV, and that OC emissions represented 36 and 43 % of total PM2.5 emissions from LDV and HDV, respectively. More than 700 ions were identified by TD-PTR-MS and the EF profiles obtained from HDV and LDV exhibited distinct features. Nitrogen-containing compounds measured in the desorbed material up to 350 °C contributed around 20 % to the EF values for both types of vehicles, possibly associated with incomplete fuel burning. Additionally, 70 % of the organic compounds measured from the aerosol

  16. Particulate matter in urban areas: health-based economic assessment.

    PubMed

    El-Fadel, M; Massoud, M

    2000-08-10

    The interest in the association between human health and air pollution has grown substantially in recent years. Based on epidemiological studies in several countries, there is conclusive evidence of a link between particulate air pollution and adverse health effects. Considering that particulate matter may be the most serious pollutant in urban areas and that pollution-related illness results in financial and non-financial welfare losses, the main objective of this study is to assess the economic benefits of reducing particulate air pollution in Lebanese urban areas. Accordingly, the extent and value of health benefits due to decreasing levels of particulate in the air are predicted. Health impacts are expressed in both physical and monetary terms for saved statistical lives, and productivity due to different types of morbidity endpoints. Finally, the study concludes with a range of policy options available to mitigate particulate air pollution in urban areas.

  17. Aerodynamic size distribution of suspended particulate matter in the ambient air in the city of Cleveland, Ohio

    NASA Technical Reports Server (NTRS)

    Leibecki, H. F.; King, R. B.; Fordyce, J. S.

    1974-01-01

    The City of Cleveland Division of Air Pollution Control and NASA jointly investigated the chemical and physical characteristics of the suspended particulate matter in Cleveland, and as part of the program, measurements of the particle size distribution of ambient air samples at five urban locations during August and September 1972 were made using high-volume cascade impactions. The distributions were evaluated for lognormality, and the mass median diameters were compared between locations and as a function of resultant wind direction. Junge-type distributions were consistent with dirty continental aerosols. About two-thirds of the suspended particulate matter observed in Cleveland is less than 7 microns in diameter.

  18. Global Chemical Composition of Ambient Fine Particulate Matter for Exposure Assessment

    PubMed Central

    2015-01-01

    Epidemiologic and health impact studies are inhibited by the paucity of global, long-term measurements of the chemical composition of fine particulate matter. We inferred PM2.5 chemical composition at 0.1° × 0.1° spatial resolution for 2004–2008 by combining aerosol optical depth retrieved from the MODIS and MISR satellite instruments, with coincident profile and composition information from the GEOS-Chem global chemical transport model. Evaluation of the satellite-model PM2.5 composition data set with North American in situ measurements indicated significant spatial agreement for secondary inorganic aerosol, particulate organic mass, black carbon, mineral dust, and sea salt. We found that global population-weighted PM2.5 concentrations were dominated by particulate organic mass (11.9 ± 7.3 μg/m3), secondary inorganic aerosol (11.1 ± 5.0 μg/m3), and mineral dust (11.1 ± 7.9 μg/m3). Secondary inorganic PM2.5 concentrations exceeded 30 μg/m3 over East China. Sensitivity simulations suggested that population-weighted ambient PM2.5 from biofuel burning (11 μg/m3) could be almost as large as from fossil fuel combustion sources (17 μg/m3). These estimates offer information about global population exposure to the chemical components and sources of PM2.5. PMID:25343705

  19. Time course of bronchial cell inflammation following exposure to diesel particulate matter using a modified EAVES.

    PubMed

    Hawley, Brie; McKenna, Dave; Marchese, Anthony; Volckens, John

    2014-08-01

    Electrostatic deposition of particles onto the surface of well-differentiated airway cells is a rapid and efficient means to screen for toxicity associated with exposure to fine and ultrafine particulate air pollution. This work describes the development and application of an electrostatic aerosol in vitro exposure system (EAVES) with increased throughput and ease-of-use. The modified EAVES accommodates standard tissue culture plates and uses an alternating electric field to deposit a net neutral charge of aerosol onto air-interface cell cultures. Using this higher-throughput design, we were able to examine the time-course (1, 3, 6, 9, and 24 h post-exposure) of transcript production and cytotoxicity in well-differentiated human bronchial cells exposed to diesel particulate matter at levels of 'real-world' significance. Statistically significant responses were observed at exposure levels (∼0.4 μg/cm(2)) much lower than typically reported in vitro using traditional submerged/resuspended techniques. Levels of HO-1, IL-8, CYP1A1, COX-2, and HSP-70 transcripts increased immediately following diesel particulate exposure and persisted for several hours; cytotoxicity was increased at 24h. The modified EAVES provides a platform for higher throughput, more efficient and representative testing of aerosol toxicity in vitro.

  20. Global Chemical Composition of Ambient Fine Particulate Matter for Exposure Assessment

    DOE PAGES

    Philip, Sajeev; Martin, Randall V.; van Donkelaar, Aaron; ...

    2014-10-24

    Epidemiologic and health impact studies are inhibited by the paucity of global, long-term measurements of the chemical composition of fine particulate matter. We inferred PM2.5 chemical composition at 0.1° × 0.1° spatial resolution for 2004–2008 by combining aerosol optical depth retrieved from the MODIS and MISR satellite instruments, with coincident profile and composition information from the GEOS-Chem global chemical transport model. Evaluation of the satellite-model PM2.5 composition data set with North American in situ measurements indicated significant spatial agreement for secondary inorganic aerosol, particulate organic mass, black carbon, mineral dust, and sea salt. We found that global population-weighted PM2.5 concentrationsmore » were dominated by particulate organic mass (11.9 ± 7.3 μg/m3), secondary inorganic aerosol (11.1 ± 5.0 μg/m3), and mineral dust (11.1 ± 7.9 μg/m3). Secondary inorganic PM2.5 concentrations exceeded 30 μg/m3 over East China. Sensitivity simulations suggested that population-weighted ambient PM2.5 from biofuel burning (11 μg/m3) could be almost as large as from fossil fuel combustion sources (17 μg/m3). In conclusion, these estimates offer information about global population exposure to the chemical components and sources of PM2.5.« less

  1. Laboratory Measurements of Particulate Matter Concentrations from Asphalt Pavement Abrasion

    NASA Astrophysics Data System (ADS)

    Fullová, Daša; Đurčanská, Daniela

    2016-12-01

    The issue of emissions from road traffic is compounded by the fact that the number of vehicles and driven kilometres increase each year. Road traffic is one of the main sources of particulate matter and traffic volume is still increasing and has unpleasant impact on longevity of the pavements and the environment. Vehicle motions cause mechanical wearing of the asphalt pavement surface - wearing course by vehicle tyres. The contribution deals with abrasion of bituminous wearing courses of pavements. The asphalt mixtures of wearing courses are compared in terms of mechanically separated particulate matter. The samples of asphalt mixtures were rutted in wheel tracking machine. The particulate matter measurements were performed in laboratory conditions. The experimental laboratory measurements make it possible to sample particulates without contamination from exhaust emissions, abraded particles from vehicles, resuspension of road dust and climate affects. The contribution offers partial results of measurements on six trial samples of asphalt mixtures with different composition. It presents particulate matter morphology and the comparison of rutted asphalt samples in terms of PM mass concentrations and chemical composition.

  2. An evaluation of indoor and outdoor biological particulate matter

    NASA Astrophysics Data System (ADS)

    Menetrez, M. Y.; Foarde, K. K.; Esch, R. K.; Schwartz, T. D.; Dean, T. R.; Hays, M. D.; Cho, S. H.; Betancourt, D. A.; Moore, S. A.

    The incidences of allergies, allergic diseases and asthma are increasing world wide. Global climate change is likely to impact plants and animals, as well as microorganisms. The World Health Organization, U.S. Environmental Protection Agency, U.S. Department of Agriculture, U.S. Department of Health and Human Services, and the Intergovernmental Panel on Climate Change cite increased allergic reactions due to climate change as a growing concern. Monitoring of indoor and ambient particulate matter (PM) and the characterization of the content for biological aerosol concentrations has not been extensively performed. Samples from urban and rural North Carolina (NC), and Denver (CO), were collected and analyzed as the goal of this research. A study of PM 10 (<10 μm in aerodynamic diameter) and PM 2.5 (<2.5 μm in aerodynamic diameter) fractions of ambient bioaerosols was undertaken for a six month period to evaluate the potential for long-term concentrations. These airborne bioaerosols can induce irritational, allergic, infectious, and chemical responses in exposed individuals. Three separate sites were monitored, samples were collected and analyzed for mass and biological content (endotoxins, (1,3)-β- D-glucan and protein). Concentrations of these bioaerosols were reported as a function of PM size fraction, mass and volume of air sampled. The results indicated that higher concentrations of biologicals were present in PM 10 than were present in PM 2.5, except when near-roadway conditions existed. This study provides the characterization of ambient bioaerosol concentrations in a variety of areas and conditions.

  3. From Source to City: Particulate Matter Concentration and Size Distribution Data from an Icelandic Dust Storm

    NASA Astrophysics Data System (ADS)

    Thorsteinsson, T.; Mockford, T.; Bullard, J. E.

    2015-12-01

    Dust storms are the source of particulate matter in 20%-25% of the cases in which the PM10health limit is exceeded in Reykjavik; which occurred approximately 20 times a year in 2005-2010. Some of the most active source areas for dust storms in Iceland, contributing to the particulate matter load in Reykjavik, are on the south coast of Iceland, with more than 20 dust storm days per year (in 2002-2011). Measurements of particle matter concentration and size distribution were recorded at Markarfljot in May and June 2015. Markarfljot is a glacial river that is fed by Eyjafjallajokull and Myrdalsjokull, and the downstream sandur areas have been shown to be significant dust sources. Particulate matter concentration during dust storms was recorded on the sandur area using a TSI DustTrak DRX Aerosol Monitor 8533 and particle size data was recorded using a TSI Optical Particle Sizer 3330 (OPS). Wind speed was measured using cup anemometers at five heights. Particle size measured at the source area shows an extremely fine dust creation, PM1 concentration reaching over 5000 μg/m3 and accounting for most of the mass. This is potentially due to sand particles chipping during saltation instead of breaking uniformly. Dust events occurring during easterly winds were captured by two permanent PM10 aerosol monitoring stations in Reykjavik (140 km west of Markarfljot) suggesting the regional nature of these events. OPS measurements from Reykjavik also provide an interesting comparison of particle size distribution from source to city. Dust storms contribute to the particular matter pollution in Reykjavik and their small particle size, at least from this source area, might be a serious health concern.

  4. Monitoring Particulate Matter with Commodity Hardware

    NASA Astrophysics Data System (ADS)

    Holstius, David

    Health effects attributed to outdoor fine particulate matter (PM 2.5) rank it among the risk factors with the highest health burdens in the world, annually accounting for over 3.2 million premature deaths and over 76 million lost disability-adjusted life years. Existing PM2.5 monitoring infrastructure cannot, however, be used to resolve variations in ambient PM2.5 concentrations with adequate spatial and temporal density, or with adequate coverage of human time-activity patterns, such that the needs of modern exposure science and control can be met. Small, inexpensive, and portable devices, relying on newly available off-the-shelf sensors, may facilitate the creation of PM2.5 datasets with improved resolution and coverage, especially if many such devices can be deployed concurrently with low system cost. Datasets generated with such technology could be used to overcome many important problems associated with exposure misclassification in air pollution epidemiology. Chapter 2 presents an epidemiological study of PM2.5 that used data from ambient monitoring stations in the Los Angeles basin to observe a decrease of 6.1 g (95% CI: 3.5, 8.7) in population mean birthweight following in utero exposure to the Southern California wildfires of 2003, but was otherwise limited by the sparsity of the empirical basis for exposure assessment. Chapter 3 demonstrates technical potential for remedying PM2.5 monitoring deficiencies, beginning with the generation of low-cost yet useful estimates of hourly and daily PM2.5 concentrations at a regulatory monitoring site. The context (an urban neighborhood proximate to a major goods-movement corridor) and the method (an off-the-shelf sensor costing approximately USD $10, combined with other low-cost, open-source, readily available hardware) were selected to have special significance among researchers and practitioners affiliated with contemporary communities of practice in public health and citizen science. As operationalized by

  5. Particulate matter, air quality and climate: lessons learned and future needs

    NASA Astrophysics Data System (ADS)

    Fuzzi, S.; Baltensperger, U.; Carslaw, K.; Decesari, S.; Denier van der Gon, H.; Facchini, M. C.; Fowler, D.; Koren, I.; Langford, B.; Lohmann, U.; Nemitz, E.; Pandis, S.; Riipinen, I.; Rudich, Y.; Schaap, M.; Slowik, J.; Spracklen, D. V.; Vignati, E.; Wild, M.; Williams, M.; Gilardoni, S.

    2015-01-01

    The literature on atmospheric particulate matter (PM), or atmospheric aerosol, has increased enormously over the last two decades and amounts now to some 1500-2000 papers per year in the refereed literature. This is in part due to the enormous advances in measurement technologies, which has allowed for an increasingly accurate understanding of the chemical composition and of the physical properties of atmospheric particles and of their processes in the atmosphere. The growing scientific interest in atmospheric aerosol particles is due to their high importance for environmental policy. In fact, particulate matter constitutes one of the most challenging problems both for air quality and climate change policies. In this context, this paper reviews the most recent results within the atmospheric aerosol science, and the policy needs, which have driven much of the increase in monitoring and mechanistic research over the last two decades. The synthesis reveals many new processes and developments in the science underpinning climate-aerosol interactions and effects of PM on human health and the environment. But, while airborne particulate matter is responsible for globally important effects on premature human mortality, we still do not know the relative importance of different chemical components of PM for these effects. Likewise, the magnitude of the overall effects of PM on climate remains highly uncertain. Despite the uncertainty there are many things that could be done to mitigate local and global problems of atmospheric PM. Recent analyses have shown that reducing BC emissions, using known control measures would reduce global warming and delay the time when anthropogenic effects on global temperature would exceed 2 °C. Likewise, cost effective control measures on ammonia, an important agricultural precursor gas for secondary inorganic aerosols (SIA), would reduce regional eutrophication and PM concentrations in large areas of Europe, China, and the USA. Thus there is

  6. Particulate matter, air quality and climate: lessons learned and future needs

    NASA Astrophysics Data System (ADS)

    Fuzzi, S.; Baltensperger, U.; Carslaw, K.; Decesari, S.; Denier van der Gon, H.; Facchini, M. C.; Fowler, D.; Koren, I.; Langford, B.; Lohmann, U.; Nemitz, E.; Pandis, S.; Riipinen, I.; Rudich, Y.; Schaap, M.; Slowik, J. G.; Spracklen, D. V.; Vignati, E.; Wild, M.; Williams, M.; Gilardoni, S.

    2015-07-01

    The literature on atmospheric particulate matter (PM), or atmospheric aerosol, has increased enormously over the last 2 decades and amounts now to some 1500-2000 papers per year in the refereed literature. This is in part due to the enormous advances in measurement technologies, which have allowed for an increasingly accurate understanding of the chemical composition and of the physical properties of atmospheric particles and of their processes in the atmosphere. The growing scientific interest in atmospheric aerosol particles is due to their high importance for environmental policy. In fact, particulate matter constitutes one of the most challenging problems both for air quality and for climate change policies. In this context, this paper reviews the most recent results within the atmospheric aerosol sciences and the policy needs, which have driven much of the increase in monitoring and mechanistic research over the last 2 decades. The synthesis reveals many new processes and developments in the science underpinning climate-aerosol interactions and effects of PM on human health and the environment. However, while airborne particulate matter is responsible for globally important influences on premature human mortality, we still do not know the relative importance of the different chemical components of PM for these effects. Likewise, the magnitude of the overall effects of PM on climate remains highly uncertain. Despite the uncertainty there are many things that could be done to mitigate local and global problems of atmospheric PM. Recent analyses have shown that reducing black carbon (BC) emissions, using known control measures, would reduce global warming and delay the time when anthropogenic effects on global temperature would exceed 2 °C. Likewise, cost-effective control measures on ammonia, an important agricultural precursor gas for secondary inorganic aerosols (SIA), would reduce regional eutrophication and PM concentrations in large areas of Europe, China

  7. 40 CFR 60.472 - Standards for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... matter in excess of 0.67 kg/Mg (1.3 lb/ton) of asphalt charged to the still when a catalyst is added to... still when a catalyst is added to the still and when No. 6 fuel oil is fired in the afterburner; and (3... a catalyst; and (4) Particulate matter in excess of 0.64 kg/Mg (1.3 lb/ton) of asphalt charged...

  8. 40 CFR 60.472 - Standards for particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... matter in excess of 0.67 kg/Mg (1.3 lb/ton) of asphalt charged to the still when a catalyst is added to... still when a catalyst is added to the still and when No. 6 fuel oil is fired in the afterburner; and (3... a catalyst; and (4) Particulate matter in excess of 0.64 kg/Mg (1.3 lb/ton) of asphalt charged...

  9. 40 CFR 60.472 - Standards for particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... matter in excess of 0.67 kg/Mg (1.3 lb/ton) of asphalt charged to the still when a catalyst is added to... still when a catalyst is added to the still and when No. 6 fuel oil is fired in the afterburner; and (3... a catalyst; and (4) Particulate matter in excess of 0.64 kg/Mg (1.3 lb/ton) of asphalt charged...

  10. Black carbon and elemental concentration of ambient particulate matter in Makassar Indonesia

    NASA Astrophysics Data System (ADS)

    Sattar, Y.; Rashid, M.; Ramli, M.; Sabariah, B.

    2014-02-01

    Airborne particulate matter with aerodynamic diameter of less or equal to 10 um or PM10, has been collected on a weekly basis for one year from February 2012 to January 2013 at one site of Makassar, Province of South Sulawesi Indonesia. The samples were collected using a size selective high volume air sampler sited at Daya, a mixed urban, commercial and industrial area in the city of Makassar. The concentration of black carbon (BC) along with a total of 14 elements (i.e Al, Ba, Ca, Cr, Fe, K, Mg, Ba, Na, Ni, Pb, Si, Ti and Zn) were determined from the sample. Results showed that the average particulate mass concentration was 32.9 ± 11.6 μg/m3 with BC and elemental concentration constituted 6.1% and 10.6% of the particulate concentration, respectively. Both BC and elemental constituents contributed 16.7% while 83.3% of the particulate matter remained to be counted for. The black carbon concentration was higher during the dry months which may be attributed to rampant biomass burning during hot and dry weather conditions, apart from other possible sources. Most of the elements were enriched relative to soil origin illustrating of their possible associations with other sources such as marine and anthropogenic derived aerosols, particularly Cr, Ni, Pb, and Zn, which are known to originate from man-made activities.

  11. Electrically heated particulate matter filter with recessed inlet end plugs

    DOEpatents

    Gonze, Eugene V [Pinckney, MI; Ament, Frank [Troy, MI

    2012-02-21

    A particulate matter (PM) filter includes filter walls having inlet ends and outlet ends. First adjacent pairs of the filter walls define inlet channels. Second adjacent pairs of the filter walls define outlet channels. Outlet end plugs are arranged in the inlet channels adjacent to the output ends. Inlet end plugs arranged in the outlet channels spaced from the inlet ends.

  12. A POPULATION EXPOSURE MODEL FOR PARTICULATE MATTER: SHEDS-PM

    EPA Science Inventory

    The US EPA National Exposure Research Laboratory (NERL) has developed a population exposure and dose model for particulate matter (PM) that will be publicly available in Fall 2002. The Stochastic Human Exposure and Dose Simulation (SHEDS-PM) model uses a probabilistic approach ...

  13. SPATIO-TEMPORAL MODELING OF FINE PARTICULATE MATTER

    EPA Science Inventory

    Studies indicate that even short-term exposure to high concentrations of fine atmospheric particulate matter (PM2.5) can lead to long-term health effects. In this paper, we propose a random effects model for PM2.5 concentrations. In particular, we anticipa...

  14. 40 CFR 60.42 - Standard for particulate matter (PM).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Fossil-Fuel-Fired Steam Generators § 60.42 Standard for particulate matter (PM). (a) Except as provided... fossil fuel or fossil fuel and wood residue. (2) Exhibit greater than 20 percent opacity except for one... owner or operator of an affected facility that combusts only gaseous or liquid fossil fuel...

  15. 40 CFR 60.42 - Standard for particulate matter (PM).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... Fossil-Fuel-Fired Steam Generators § 60.42 Standard for particulate matter (PM). (a) Except as provided... fossil fuel or fossil fuel and wood residue. (2) Exhibit greater than 20 percent opacity except for one... owner or operator of an affected facility that combusts only gaseous or liquid fossil fuel...

  16. 40 CFR 60.42 - Standard for particulate matter (PM).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Fossil-Fuel-Fired Steam Generators § 60.42 Standard for particulate matter (PM). (a) Except as provided... fossil fuel or fossil fuel and wood residue. (2) Exhibit greater than 20 percent opacity except for one... owner or operator of an affected facility that combusts only gaseous or liquid fossil fuel...

  17. 40 CFR 60.142a - Standards for particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 20, 1983 § 60.142a Standards for particulate matter. (a) Except as provided under paragraphs (b) and... the steel production cycle of any top-blown BOPF or during hot metal transfer or skimming operations... secondary emissions from a top-blown BOPF or from hot metal transfer or skimming for a top-blown or a...

  18. AN EVALUATION OF THE PROTEIN MASS OF PARTICULATE MATTER

    EPA Science Inventory

    A comparison of ambient particulate matter mass concentrations with the total protein mass concentration has not been performed previously for North Carolina and was the goal of this study. The analysis of total protein mass was used as an all inclusive indicator of biologically ...

  19. 40 CFR 60.172 - Standard for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standard for particulate matter. 60.172 Section 60.172 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES Standards of Performance for Primary...

  20. 40 CFR 60.172 - Standard for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standard for particulate matter. 60.172 Section 60.172 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES Standards of Performance for Primary...

  1. 40 CFR 60.172 - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.172 Section 60.172 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES Standards of Performance for Primary...

  2. OXIDATIVE STRESS PARTICIPATES IN PARTICULATE MATTER (PM) INDUCED LUNG INJURY

    EPA Science Inventory

    Oxidative stress participates in particulate matter (PM) induced acute lung injury.
    Elizabeth S. Roberts1, Judy L. Richards2, Kevin L. Dreher2. 1College of Veterinary Medicine, NC State University, Raleigh, NC, 2US Environmental Protection Agency, NHEERL, RTP, NC.
    Epidemiol...

  3. Turkish Pupils' Conceptions of the Particulate Nature of Matter

    ERIC Educational Resources Information Center

    Boz, Yezdan

    2006-01-01

    The purpose of this research study is to explore year 6, 8 & 11 (13, 15 and 17 years old respectively) Turkish pupils' views about the particulate nature of matter within the context of phase changes. About 300 pupils participated in the study. Questionnaires distributed to year 6, 8 and 11 pupils included 6-item open-ended questions about (a)…

  4. Characterization of cotton gin particulate matter emissions - project plan

    Technology Transfer Automated Retrieval System (TEKTRAN)

    In 2006, EPA implemented a more stringent standard for particulate matter with an effective diameter less than 2.5 microns (PM2.5). The implementation time line for this standard will vary by state/district regulatory agency. For example, the San Joaquin Valley Air Pollution Control District has pro...

  5. Characterization of cotton gin particulate matter emissions – project plan

    Technology Transfer Automated Retrieval System (TEKTRAN)

    In 2006, EPA implemented a more stringent standard for particulate matter with an effective diameter less than 2.5 microns (PM2.5). The implementation timeline for this standard will vary by state/district regulatory agency. For example, the San Joaquin Valley Air Pollution Control District, has pro...

  6. SOURCE SAMPLING FINE PARTICULATE MATTER: WOOD-FIRED INDUSTRIAL BOILER

    EPA Science Inventory

    The report provides a profile for a wood-fired industrial boiler equipped with a multistage electrostatic precipitator control device. Along with the profile of emissions of fine particulate matter of aerodynamic diameter of 2.5 micrometers or less (PM-2.5), data are also provide...

  7. Particulate matter adjacent to cattle deep-bedded monoslope facilities

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Purpose: Confined cattle facilities are an increasingly common housing system in the Northern Great Plains region. Many of these facilities add organic bedding material to the pens once or twice per week. Particulate matter concentrations and emissions from these facilities have not been evaluate...

  8. 40 CFR 60.402 - Standard for particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES Standards of Performance for Phosphate Rock... subpart shall cause to be discharged into the atmosphere: (1) From any phosphate rock dryer any gases which: (i) Contain particulate matter in excess of 0.030 kilogram per megagram of phosphate rock feed...

  9. 40 CFR 60.402 - Standard for particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES Standards of Performance for Phosphate Rock... subpart shall cause to be discharged into the atmosphere: (1) From any phosphate rock dryer any gases which: (i) Contain particulate matter in excess of 0.030 kilogram per megagram of phosphate rock feed...

  10. Concentrations of particulate matter in large cattle feedlots in Kansas

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Air quality in communities surrounding cattle feedlots is a growing public concern. Our objective was to quantify emission patterns and weather effects on particulate matter (PM) transport upwind and downwind from two large cattle feedlots (KS1, KS2) in Kansas. The concentrations of PM2.5 (particles...

  11. Respiratory dose analysis for components of ambient particulate matter

    EPA Science Inventory

    Particulate matter (PM) in the atmosphere is a complex mixture of particles with different sizes and chemical compositions. Although PM is known to induce health effects, specific attributes of PM that may cause health effects are somewhat ambiguous. Dose of each specific compone...

  12. 40 CFR 52.776 - Control strategy: Particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 3 2010-07-01 2010-07-01 false Control strategy: Particulate matter... PROGRAMS (CONTINUED) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Indiana § 52.776 Control strategy... Metropolitan Indianapolis Intrastate Region. (b) APC 4-R of Indiana's “Air Pollution Control...

  13. Air Quality Criteria for Particulate Matter (Final Report, 2004)

    EPA Science Inventory

    EPA has completed the process of updating and revising, where appropriate, its Air Quality Criteria for Particulate Matter (PM) as issued in 1996 (usually referred to as the Criteria Document). Sections 108 and 109 of the Clean Air Act require that EPA carry out a periodic revi...

  14. 40 CFR 60.62 - Standard for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.62 Section 60.62 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES Standards of Performance for Portland...

  15. Integrated Science Assessment for Particulate Matter (Second External Review Draft)

    EPA Science Inventory

    EPA has announced that the Second External Review Draft of the Integrated Science Assessment (ISA) for Particulate Matter (PM) have been made available for independent peer review and public review. The ISA reflects the latest scientific knowledge useful in indicating the kind...

  16. Inductively heated particulate matter filter regeneration control system

    SciTech Connect

    Gonze, Eugene V; Paratore Jr., Michael J; Kirby, Kevin W; Phelps, Amanda; Gregoire, Daniel J

    2012-10-23

    A system includes a particulate matter (PM) filter with an upstream end for receiving exhaust gas, a downstream end and zones. The system also includes a heating element. A control module selectively activates the heating element to inductively heat one of the zones.

  17. 40 CFR 60.732 - Standards for particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES Standards of Performance for Calciners and... particulate matter in excess of 0.092 gram per dry standard cubic meter (g/dscm) for calciners and for calciners and dryers installed in series and in excess of 0.057 g/dscm (0.025 gr/dscf) for dryers; and...

  18. 40 CFR 60.732 - Standards for particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES Standards of Performance for Calciners and... particulate matter in excess of 0.092 gram per dry standard cubic meter (g/dscm) for calciners and for calciners and dryers installed in series and in excess of 0.057 g/dscm (0.025 gr/dscf) for dryers; and...

  19. 40 CFR 60.732 - Standards for particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES Standards of Performance for Calciners and... particulate matter in excess of 0.092 gram per dry standard cubic meter (g/dscm) for calciners and for calciners and dryers installed in series and in excess of 0.057 g/dscm (0.025 gr/dscf) for dryers; and...

  20. 40 CFR 60.732 - Standards for particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES Standards of Performance for Calciners and... particulate matter in excess of 0.092 gram per dry standard cubic meter (g/dscm) for calciners and for calciners and dryers installed in series and in excess of 0.057 g/dscm (0.025 gr/dscf) for dryers; and...

  1. 40 CFR 60.732 - Standards for particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES Standards of Performance for Calciners and... particulate matter in excess of 0.092 gram per dry standard cubic meter (g/dscm) for calciners and for calciners and dryers installed in series and in excess of 0.057 g/dscm (0.025 gr/dscf) for dryers; and...

  2. 40 CFR 266.105 - Standards to control particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... standard cubic foot) after correction to a stack gas concentration of 7% oxygen, using procedures... particulate matter standard. (c) Oxygen correction. (1) Measured pollutant levels must be corrected for the amount of oxygen in the stack gas according to the formula: ER30SE99.027 Where: Pc is the...

  3. EXPOSURE ASSESSMENT OF PARTICULATE MATTER FOR SUSCEPTIBLE POPULATIONS IN SEATTLE

    EPA Science Inventory

    In this article we present results from a 2-year comprehensive exposure assessment study that examined the particulate matter (PM) exposures and health effects in 108 individuals with and without chronic obstructive pulmonary disease (COPD), coronary heart disease (CHD), and as...

  4. Integrated Science Assessment for Particulate Matter (First External Review Draft)

    EPA Science Inventory

    EPA has announced that the First External Review Draft of the Integrated Science Assessment (ISA) for Particulate Matter and related Annexes have been made available for independent peer review and public review. This draft ISA document represents a concise synthesis and e...

  5. Particulate matter neurotoxicity in culture is size-dependent

    EPA Science Inventory

    Exposure to particulate matter (PM) air pollution produces inflammatory damage to the cardiopulmonary system. This toxicity appears to be inversely related to the size of the PM particles, with the ultrafine particle being more inflammatory than larger sizes. Exposure to PM has m...

  6. Evaluation of a Direct Personal Coarse Particulate Matter Monitor

    EPA Science Inventory

    One aspect of the North Carolina Adult Asthma and Environment study (NCAAES) was to evaluate personal exposures to coarse particulate matter (PM 10-2.5) and their associated variability. As part of this, we examined the ability of a community-based monitor to act as...

  7. Personal Coarse Particulate Matter Exposures in an Adult Cohort

    EPA Science Inventory

    Volunteers associated with the North Carolina Adult Asthma and Environment Study (NCAAES) participated in an investigation of personal daily exposures to coarse and fine particulate matter size fractions (PM10-2.5, PM2.5). Data from these personal measuremen...

  8. 2009 Final Report: Integrated Science Assessment for Particulate Matter

    EPA Science Inventory

    Cover of the Integrated Science Assessment (ISA) for <span class=Particulate Matter" vspace = "5" hspace="5" align="right" border="1" /> EPA has released the final Integrated Science Assessment (ISA) for P...

  9. 77 FR 39205 - Public Hearings for Proposed Rules-National Ambient Air Quality Standards for Particulate Matter

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-07-02

    ... Quality Standards for Particulate Matter AGENCY: Environmental Protection Agency (EPA). ACTION... titled, ``National Ambient Air Quality Standards for Particulate Matter,'' that is scheduled to be... and secondary national ambient air quality standards (NAAQS) for particulate matter (PM) to...

  10. 77 FR 50446 - Approval and Promulgation of Implementation Plans; Tennessee; Knoxville; Fine Particulate Matter...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-08-21

    ... Particulate Matter 2002 Base Year Emissions Inventory AGENCY: Environmental Protection Agency (EPA). ACTION: Proposed rule. SUMMARY: EPA is proposing to approve the 1997 annual fine particulate matter (PM 2.5 )...

  11. The heart as an extravascular target of endothelin-1 in particulate matter-induced cardiac dysfunction

    EPA Science Inventory

    Exposure to particulate matter air pollution has been causally linked to cardiovascular disease in humans. Several broad and overlapping hypotheses describing the biological mechanisms by which particulate matter exposure leads to cardiovascular disease and cardiac dysfunction ha...

  12. Analysis of particulate emissions from tropical biomass burning using a global aerosol model and long-term surface observations

    NASA Astrophysics Data System (ADS)

    Reddington, Carly L.; Spracklen, Dominick V.; Artaxo, Paulo; Ridley, David A.; Rizzo, Luciana V.; Arana, Andrea

    2016-09-01

    We use the GLOMAP global aerosol model evaluated against observations of surface particulate matter (PM2.5) and aerosol optical depth (AOD) to better understand the impacts of biomass burning on tropical aerosol over the period 2003 to 2011. Previous studies report a large underestimation of AOD over regions impacted by tropical biomass burning, scaling particulate emissions from fire by up to a factor of 6 to enable the models to simulate observed AOD. To explore the uncertainty in emissions we use three satellite-derived fire emission datasets (GFED3, GFAS1 and FINN1). In these datasets the tropics account for 66-84 % of global particulate emissions from fire. With all emission datasets GLOMAP underestimates dry season PM2.5 concentrations in regions of high fire activity in South America and underestimates AOD over South America, Africa and Southeast Asia. When we assume an upper estimate of aerosol hygroscopicity, underestimation of AOD over tropical regions impacted by biomass burning is reduced relative to previous studies. Where coincident observations of surface PM2.5 and AOD are available we find a greater model underestimation of AOD than PM2.5, even when we assume an upper estimate of aerosol hygroscopicity. Increasing particulate emissions to improve simulation of AOD can therefore lead to overestimation of surface PM2.5 concentrations. We find that scaling FINN1 emissions by a factor of 1.5 prevents underestimation of AOD and surface PM2.5 in most tropical locations except Africa. GFAS1 requires emission scaling factor of 3.4 in most locations with the exception of equatorial Asia where a scaling factor of 1.5 is adequate. Scaling GFED3 emissions by a factor of 1.5 is sufficient in active deforestation regions of South America and equatorial Asia, but a larger scaling factor is required elsewhere. The model with GFED3 emissions poorly simulates observed seasonal variability in surface PM2.5 and AOD in regions where small fires dominate, providing

  13. Particulate Matter Filtration Design Considerations for Crewed Spacecraft Life Support Systems

    NASA Technical Reports Server (NTRS)

    Agui, Juan H.; Vijayakumar, R.; Perry, Jay L.

    2016-01-01

    Particulate matter filtration is a key component of crewed spacecraft cabin ventilation and life support system (LSS) architectures. The basic particulate matter filtration functional requirements as they relate to an exploration vehicle LSS architecture are presented. Particulate matter filtration concepts are reviewed and design considerations are discussed. A concept for a particulate matter filtration architecture suitable for exploration missions is presented. The conceptual architecture considers the results from developmental work and incorporates best practice design considerations.

  14. Fossil and nonfossil carbon in fine particulate matter: A study of five European cities

    NASA Astrophysics Data System (ADS)

    Glasius, Marianne; La Cour, Agnete; Lohse, Christian

    2011-06-01

    Fossil carbon in particulate matter comes from anthropogenic use and combustion of fossil fuels, while nonfossil carbon may originate from both biogenic (e.g., pollen, plant debris, fungal spores, and biogenic secondary organic aerosol (SOA)) and anthropogenic sources (e.g., cooking and residential wood combustion). We investigated the relative contributions of fossil and nonfossil sources to fine carbonaceous aerosols in five European cities by radiocarbon analysis of aerosol samples collected at four types of sites in 2002-2004. The average fraction of nonfossil carbon was 43 ± 11%, with the lowest fraction, 36 ± 7%, at urban curbside sites and the highest fraction, 54 ± 11%, at rural background sites, farthest away from the impact of man-made emissions. Generally, fossil carbon concentrations at urban curbside sites are elevated in comparison to background sites, which is expected because of their proximity to vehicular emissions. Contrary to what might be expected, the concentration of nonfossil carbon is also higher at curbside than at background sites. This may be attributable to differences between site categories in levels of primary biological aerosols, brake and tire wear in resuspended road dust, biofuels, emissions from cooking and residential wood combustion, or processes such as anthropogenic enhancement of biogenic SOA and increased partitioning of semivolatile compounds into the aerosol phase at urban sites. The exact causes should be investigated by future detailed source analyses.

  15. Stroke Damage Is Exacerbated by Nano-Size Particulate Matter in a Mouse Model.

    PubMed

    Liu, Qinghai; Babadjouni, Robin; Radwanski, Ryan; Cheng, Hank; Patel, Arati; Hodis, Drew M; He, Shuhan; Baumbacher, Peter; Russin, Jonathan J; Morgan, Todd E; Sioutas, Constantinos; Finch, Caleb E; Mack, William J

    2016-01-01

    This study examines the effects of nano-size particulate matter (nPM) exposure in the setting of murine reperfused stroke. Particulate matter is a potent source of inflammation and oxidative stress. These processes are known to influence stroke progression through recruitment of marginally viable penumbral tissue into the ischemic core. nPM was collected in an urban area in central Los Angeles, impacted primarily by traffic emissions. Re-aerosolized nPM or filtered air was then administered to mice through whole body exposure chambers for forty-five cumulative hours. Exposed mice then underwent middle cerebral artery occlusion/ reperfusion. Following cerebral ischemia/ reperfusion, mice exposed to nPM exhibited significantly larger infarct volumes and less favorable neurological deficit scores when compared to mice exposed to filtered air. Mice exposed to nPM also demonstrated increases in markers of inflammation and oxidative stress in the region of the ischemic core. The findings suggest a detrimental effect of urban airborne particulate matter exposure in the setting of acute ischemic stroke.

  16. Stroke Damage Is Exacerbated by Nano-Size Particulate Matter in a Mouse Model

    PubMed Central

    Liu, Qinghai; Babadjouni, Robin; Radwanski, Ryan; Cheng, Hank; Patel, Arati; Hodis, Drew M.; He, Shuhan; Baumbacher, Peter; Russin, Jonathan J.; Morgan, Todd E.; Sioutas, Constantinos; Finch, Caleb E.; Mack, William J.

    2016-01-01

    This study examines the effects of nano-size particulate matter (nPM) exposure in the setting of murine reperfused stroke. Particulate matter is a potent source of inflammation and oxidative stress. These processes are known to influence stroke progression through recruitment of marginally viable penumbral tissue into the ischemic core. nPM was collected in an urban area in central Los Angeles, impacted primarily by traffic emissions. Re-aerosolized nPM or filtered air was then administered to mice through whole body exposure chambers for forty-five cumulative hours. Exposed mice then underwent middle cerebral artery occlusion/ reperfusion. Following cerebral ischemia/ reperfusion, mice exposed to nPM exhibited significantly larger infarct volumes and less favorable neurological deficit scores when compared to mice exposed to filtered air. Mice exposed to nPM also demonstrated increases in markers of inflammation and oxidative stress in the region of the ischemic core. The findings suggest a detrimental effect of urban airborne particulate matter exposure in the setting of acute ischemic stroke. PMID:27071057

  17. PRELIMINARY PARTICULATE MATTER MASS CONCENTRATIONS ASSOCIATED WITH LONGITUDINAL PANEL STUDIES "ASSESSING HUMAN EXPOSURES OF HIGH RISK SUBPOPULATIONS TO PARTICULATE MATTER"

    EPA Science Inventory

    The NERL Particulate Matter Longitudinal Panel Studies were used to characterize temporal variations of personal exposure to PM and related co-pollutants, including that of PM measured at ambient sites. These studies were fundamental in understanding the associations between p...

  18. Characterisation of local and external contributions of atmospheric particulate matter at a background coastal site

    NASA Astrophysics Data System (ADS)

    Salvador, Pedro; Artíñano, Begoña; Querol, Xavier; Alastuey, Andrés; Costoya, Miguel

    This study applies a methodology for discriminating local and external contributions of atmospheric particulate matter (PM) at a rural background station in the North-western coast of Spain. The main inputs at the nearest scale have come from soil dust, marine aerosol and road traffic. At a larger scale, the highest contributions have come from fossil-fuel combustion sources, giving rise to relatively high ammonium sulphate background levels, mainly in summer. External contributions from long-range transport processes of African dust and nitrate have been detected. Morocco and Western Sahara have been identified as the main potential source regions of African dust, with a higher content of Al and Ti than other crustal components. Geographical areas from central and Eastern Europe have been identified as potential sources of particulate nitrate. The discrimination of the PM contribution from natural and anthropogenic sources at different geographical scales is a necessary information for establishing PM reduction strategies in specific areas.

  19. 75 FR 17894 - Approval and Promulgation of Air Quality Implementation Plans; Wisconsin; Particulate Matter...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-04-08

    ...; Particulate Matter Standards AGENCY: Environmental Protection Agency (EPA). ACTION: Proposed rule. SUMMARY... September 11, 2009. EPA revised its particulate matter standards in October 2006 by strengthening the 24... particulate matter. DATES: Comments must be received on or before May 10, 2010. ADDRESSES: Submit...

  20. Global Fine Particulate Matter Concentrations and Trends Inferred from Satellite Observations, Modeling, and Ground-Based Measurements

    NASA Astrophysics Data System (ADS)

    Martin, Randall; van Donkelaar, Aaron; Boys, Brian; Philip, Sajeev; Lee, Colin; Snider, Graydon; Weagle, Crystal

    2014-05-01

    Outdoor fine particulate matter (PM2.5) is a leading environmentally-related cause of premature mortality worldwide. However, ground-level PM2.5 monitors remain sparse in many regions of the world. Satellite remote sensing from MODIS, MISR, and SeaWiFS yields a powerful global data source to address this issue. Global modeling (GEOS-Chem) plays a critical role in relating these observations to ground-level concentrations. The resultant satellite-based estimates of PM2.5 indicate dramatic variation around the world, with implications for global public health. A new ground-based aerosol network (SPARTAN) offers valuable measurements to understand the relationship between satellite observations of aerosol optical depth and ground-level PM2.5 concentrations. This talk will highlight recent advances in combining satellite remote sensing, global modeling, and ground-based measurements to improve understanding of global population exposure to outdoor fine particulate matter.

  1. Calculating the potential to emit particulate matter

    SciTech Connect

    Vaart, D.R. van der

    1996-09-01

    As the implementation of the 1990 amendments to the Clean Air Act, and Title V in particular, continues, questions regarding the calculation of a facility`s potential to emit continue to surface. The US Environmental Protection Agency (EPA) has provided limited guidance decisions, although many are still being made during Title V implementation. This paper discusses what is meant by PM-10 and the validity of using sieve analysis in estimating particulate emissions. Title V of the Clean Air Amendments of 1990, and the accompanying regulations in 40 CFR Part 70, defines a major source subject to Title V by calculating its potential emissions of all regulated pollutants, both criteria and hazardous air pollutants. For PM, the threshold emission rate is 100 tons per year (tpy) for applicability to Title V. Much discussion has ensued regarding a definition of PM for the purpose of determining a facility`s potential to emit. Recently, EPA provided guidance which indicated that only PM-10 should be considered for making this determination although many states regulate larger particles through their state implementation plan (SIP) as a surrogate for PM-10.

  2. Gene-particulate matter-health interactions

    SciTech Connect

    Kleeberger, Steven R. . E-mail: kleeber1@niehs.nih.gov; Ohtsuka, Yoshinori

    2005-09-01

    Inter-individual variation in human responses to air pollutants suggests that some subpopulations are at increased risk to the detrimental effects of pollutant exposure. Extrinsic factors such as previous exposure and nutritional status may influence individual susceptibility. Intrinsic (host) factors that determine susceptibility include age, gender, and pre-existing disease (e.g., asthma), and it is becoming clear that genetic background also contributes to individual susceptibility. Environmental exposures to particulates and genetic factors associated with disease risk likely interact in a complex fashion that varies from one population and one individual to another. The relationships between genetic background and disease risk and severity are often evaluated through traditional family-based linkage studies and positional cloning techniques. However, case-control studies based on association of disease or disease subphenotypes with candidate genes have advantages over family pedigree studies for complex disease phenotypes. This is based in part on continued development of quantitative analysis and the discovery and availability of simple sequence repeats and single nucleotide polymorphisms. Linkage analyses with genetically standardized animal models also provide a useful tool to identify genetic determinants of responses to environmental pollutants. These approaches have identified significant susceptibility quantitative trait loci on mouse chromosomes 1, 6, 11, and 17. Physical mapping and comparative mapping between human and mouse genomes will yield candidate susceptibility genes that may be tested by association studies in human subjects. Human studies and mouse modeling will provide important insight to understanding genetic factors that contribute to differential susceptibility to air pollutants.

  3. Chemical characterization and source apportionment of fine and coarse particulate matter in Lahore, Pakistan

    NASA Astrophysics Data System (ADS)

    Stone, Elizabeth; Schauer, James; Quraishi, Tauseef A.; Mahmood, Abid

    2010-03-01

    Lahore, Pakistan is an emerging megacity that is heavily polluted with high levels of particle air pollution. In this study, respirable particulate matter (PM 2.5 and PM 10) were collected every sixth day in Lahore from 12 January 2007 to 19 January 2008. Ambient aerosol was characterized using well-established chemical methods for mass, organic carbon (OC), elemental carbon (EC), ionic species (sulfate, nitrate, chloride, ammonium, sodium, calcium, and potassium), and organic species. The annual average concentration (±one standard deviation) of PM 2.5 was 194 ± 94 μg m -3 and PM 10 was 336 ± 135 μg m -3. Coarse aerosol (PM 10-2.5) was dominated by crustal sources like dust (74 ± 16%, annual average ± one standard deviation), whereas fine particles were dominated by carbonaceous aerosol (organic matter and elemental carbon, 61 ± 17%). Organic tracer species were used to identify sources of PM 2.5 OC and chemical mass balance (CMB) modeling was used to estimate relative source contributions. On an annual basis, non-catalyzed motor vehicles accounted for more than half of primary OC (53 ± 19%). Lesser sources included biomass burning (10 ± 5%) and the combined source of diesel engines and residual fuel oil combustion (6 ± 2%). Secondary organic aerosol (SOA) was an important contributor to ambient OC, particularly during the winter when secondary processing of aerosol species during fog episodes was expected. Coal combustion alone contributed a small percentage of organic aerosol (1.9 ± 0.3%), but showed strong linear correlation with unidentified sources of OC that contributed more significantly (27 ± 16%). Brick kilns, where coal and other low quality fuels are burned together, are suggested as the most probable origins of unapportioned OC. The chemical profiling of emissions from brick kilns and other sources unique to Lahore would contribute to a better understanding of OC sources in this megacity.

  4. Satellite remote sensing of particulate matter and air quality assessment over global cities

    NASA Astrophysics Data System (ADS)

    Gupta, Pawan; Christopher, Sundar A.; Wang, Jun; Gehrig, Robert; Lee, Yc; Kumar, Naresh

    Using 1 year of aerosol optical thickness (AOT) retrievals from the MODerate resolution Imaging Spectro-radiometer (MODIS) on board NASA's Terra and Aqua satellite along with ground measurements of PM 2.5 mass concentration, we assess particulate matter air quality over different locations across the global urban areas spread over 26 locations in Sydney, Delhi, Hong Kong, New York City and Switzerland. An empirical relationship between AOT and PM 2.5 mass is obtained and results show that there is an excellent correlation between the bin-averaged daily mean satellite and ground-based values with a linear correlation coefficient of 0.96. Using meteorological and other ancillary datasets, we assess the effects of wind speed, cloud cover, and mixing height (MH) on particulate matter (PM) air quality and conclude that these data are necessary to further apply satellite data for air quality research. Our study clearly demonstrates that satellite-derived AOT is a good surrogate for monitoring PM air quality over the earth. However, our analysis shows that the PM 2.5-AOT relationship strongly depends on aerosol concentrations, ambient relative humidity (RH), fractional cloud cover and height of the mixing layer. Highest correlation between MODIS AOT and PM 2.5 mass is found under clear sky conditions with less than 40-50% RH and when atmospheric MH ranges from 100 to 200 m. Future remote sensing sensors such as Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) that have the capability to provide vertical distribution of aerosols will further enhance our ability to monitor and forecast air pollution. This study is among the first to examine the relationship between satellite and ground measurements over several global locations.

  5. Receptor modelling of airborne particulate matter in the vicinity of a major steelworks site.

    PubMed

    Taiwo, A M; Beddows, D C S; Calzolai, G; Harrison, Roy M; Lucarelli, F; Nava, S; Shi, Z; Valli, G; Vecchi, R

    2014-08-15

    In this study, the Multilinear Engine (ME-2) receptor model was applied to speciated particulate matter concentration data collected with two different measuring instruments upwind and downwind of a steelworks complex in Port Talbot, South Wales, United Kingdom. Hourly and daily PM samples were collected with Streaker and Partisol samplers, respectively, during a one month sampling campaign between April 18 and May 16, 2012. Daily samples (PM10, PM2.5, PM2.5-10) were analysed for trace metals and water-soluble ions using standard procedures. Hourly samples (PM2.5 and PM2.5-10) were assayed for 22 elements by Particle Induced X-ray Emission (PIXE). PM10 data analysis using ME-2 resolved 6 factors from both datasets identifying different steel processing units including emissions from the blast furnaces (BF), the basic oxygen furnace steelmaking plant (BOS), the coke-making plant, and the sinter plant. Steelworks emissions were the main contributors to PM10 accounting for 45% of the mass when including also secondary aerosol. The blast furnaces were the largest emitter of primary PM10 in the study area, explaining about one-fifth of the mass. Other source contributions to PM10 were from marine aerosol (28%), traffic (16%), and background aerosol (11%). ME-2 analysis was also performed on daily PM2.5 and PM2.5-10 data resolving 7 and 6 factors, respectively. The largest contributions to PM2.5-10 were from marine aerosol (30%) and blast furnace emissions (28%). Secondary components explained one-half of PM2.5 mass. The influence of steelworks sources on ambient particulate matter at Port Talbot was distinguishable for several separate processing sections within the steelworks in all PM fractions.

  6. Determination of trace metals in air particulate matters by capillary electrophoresis with spectrophotometric detection

    SciTech Connect

    Fung, Y.S.; Tung, H.S.

    1998-12-31

    Chemical analysis of trace metals in air particulate matters are required for studies in the apportionment of major air pollution sources, occupational health protection, environmental monitoring of ambient and indoor air, and for atmospheric aerosol research purpose. The demand for the required analysis is towards more sensitive, cheaper and automated method, as well as capability of differentiating different chemical species present in the air particulate matters. The recent advance of capillary electrophoresis provides an alternative method for multi-element determination with capability of speciation of different chemical elements for both total and leachable metal determination. It also uses equipment available in many chemical laboratories with reasonable capital and low running cost. In the present paper, the application of CE for trace metal analysis in air particulate matters will be investigated in three areas. The first area is the development of sample pretreatment method. For total metal analysis, the microwave digestion method is chosen based on short digestion time and reduced contamination. The second area is the optimization of the CE buffers. The use of strong and weak complex system is compared using histidine and 4-methylbenzylamine for indirect UV detection and 8-hydroxyquinoline-5-sulphonic acid (HQS) for direct UV detection for CE separation of alkali and alkaline earth metals (ammonium, potassium, sodium, calcium, magnesium, barium, strontium) with transition metals (cobalt, cadmium, nickel, zinc, lead and copper). The role of lactic acid, 18-crown-6 and other additives to effect satisfactory separation of closely co-migrated pairs and to achieve suitable separation of large amounts of alkali metals (ppm) from trace levels of transition metals (ppb) will be discussed for both leachable and total metals present in air particulate matters.

  7. Biodiesel Fuel Property Effects on Particulate Matter Reactivity

    SciTech Connect

    Williams, A.; Black, S.; McCormick, R. L.

    2010-06-01

    Controlling diesel particulate emissions to meet the 2007 U.S. standard requires the use of a diesel particulate filter (DPF). The reactivity of soot, or the carbon fraction of particulate matter, in the DPF and the kinetics of soot oxidation are important in achieving better control of aftertreatment devices. Studies showed that biodiesel in the fuel can increase soot reactivity. This study therefore investigated which biodiesel fuel properties impact reactivity. Three fuel properties of interest included fuel oxygen content and functionality, fuel aromatic content, and the presence of alkali metals. To determine fuel effects on soot reactivity, the performance of a catalyzed DPF was measured with different test fuels through engine testing and thermo-gravimetric analysis. Results showed no dependence on the aromatic content or the presence of alkali metals in the fuel. The presence and form of fuel oxygen was the dominant contributor to faster DPF regeneration times and soot reactivity.

  8. Radio Frequency Sensing of Particulate Matter Accumulation on a Gasoline Particulate Filter

    SciTech Connect

    Parks, James; Prikhodko, Vitaly Y.; Sappok, Alex; Ragaller, Paul; Bromberg, Leslie

    2016-10-30

    Filter Sensing Technology’s radio frequency (RF) sensor for particulate filter on-board diagnostics (OBD) was studied on a lean gasoline engine at the National Transportation Research Center (NTRC) at Oak Ridge National Laboratory (ORNL). The response of the RF sensor to particulate matter (PM) or “soot” accumulation on the gasoline particulate filter (GPF) installed in the engine exhaust was evaluated. In addition, end plugs of the GPF were purposely removed, and subsequent changes to the RF sensor measured soot loading on the GPF were characterized. Results from the study showed that the RF sensor can accurately measure soot accumulation on a GPF; furthermore, the predicted decreased soot accumulation due to plug removal was detected by the RF sensor. Overall, the studies were short and preliminary in nature; however, clearly, the RF sensor demonstrated the capability of measuring GPF soot loading at a level suitable for use in lean gasoline engine emission control OBD and control.

  9. Stable isotopes measurements reveal dual carbon pools contributing to organic matter enrichment in marine aerosol

    PubMed Central

    Ceburnis, Darius; Masalaite, Agne; Ovadnevaite, Jurgita; Garbaras, Andrius; Remeikis, Vidmantas; Maenhaut, Willy; Claeys, Magda; Sciare, Jean; Baisnée, Dominique; O’Dowd, Colin D.

    2016-01-01

    Stable carbon isotope ratios in marine aerosol collected over the Southern Indian Ocean revealed δ13C values ranging from −20.0‰ to −28.2‰. The isotope ratios exhibited a strong correlation with the fractional organic matter (OM) enrichment in sea spray aerosol. The base-level isotope ratio of −20.0‰ is characteristic of an aged Dissolved Organic Matter (DOM) pool contributing a relatively homogeneous background level of DOM to oceanic waters. The range of isotope ratios, extending down to −28.2‰, is characteristic of more variable, stronger, and fresher Particulate Organic Matter (POM) pool driven by trophic level interactions. We present a conceptual dual-pool POM-DOM model which comprises a ‘young’ and variable POM pool which dominates enrichment in sea-spray and an ‘aged’ but invariant DOM pool which is, ultimately, an aged end-product of processed ‘fresh’ POM. This model is harmonious with the preferential enrichment of fresh colloidal and nano-gel lipid-like particulate matter in sea spray particles and the observed depleted δ13C ratio resulting from isotope equilibrium fractionation coupled with enhanced plankton photosynthesis in cold water (−2 °C to +8 °C). These results re-assert the hypothesis that OM enrichment in sea-spray is directly linked to primary production and, consequently, can have implications for climate-aerosol-cloud feedback systems. PMID:27819297

  10. Stable isotopes measurements reveal dual carbon pools contributing to organic matter enrichment in marine aerosol

    NASA Astrophysics Data System (ADS)

    Ceburnis, Darius; Masalaite, Agne; Ovadnevaite, Jurgita; Garbaras, Andrius; Remeikis, Vidmantas; Maenhaut, Willy; Claeys, Magda; Sciare, Jean; Baisnée, Dominique; O’Dowd, Colin D.

    2016-11-01

    Stable carbon isotope ratios in marine aerosol collected over the Southern Indian Ocean revealed δ13C values ranging from ‑20.0‰ to ‑28.2‰. The isotope ratios exhibited a strong correlation with the fractional organic matter (OM) enrichment in sea spray aerosol. The base-level isotope ratio of ‑20.0‰ is characteristic of an aged Dissolved Organic Matter (DOM) pool contributing a relatively homogeneous background level of DOM to oceanic waters. The range of isotope ratios, extending down to ‑28.2‰, is characteristic of more variable, stronger, and fresher Particulate Organic Matter (POM) pool driven by trophic level interactions. We present a conceptual dual-pool POM-DOM model which comprises a ‘young’ and variable POM pool which dominates enrichment in sea-spray and an ‘aged’ but invariant DOM pool which is, ultimately, an aged end-product of processed ‘fresh’ POM. This model is harmonious with the preferential enrichment of fresh colloidal and nano-gel lipid-like particulate matter in sea spray particles and the observed depleted δ13C ratio resulting from isotope equilibrium fractionation coupled with enhanced plankton photosynthesis in cold water (‑2 °C to +8 °C). These results re-assert the hypothesis that OM enrichment in sea-spray is directly linked to primary production and, consequently, can have implications for climate-aerosol-cloud feedback systems.

  11. Primary particulate emissions and secondary organic aerosol (SOA) formation from idling diesel vehicle exhaust in China.

    PubMed

    Deng, Wei; Hu, Qihou; Liu, Tengyu; Wang, Xinming; Zhang, Yanli; Song, Wei; Sun, Yele; Bi, Xinhui; Yu, Jianzhen; Yang, Weiqiang; Huang, Xinyu; Zhang, Zhou; Huang, Zhonghui; He, Quanfu; Mellouki, Abdelwahid; George, Christian

    2017-03-26

    In China diesel vehicles dominate the primary emission of particulate matters from on-road vehicles, and they might also contribute substantially to the formation of secondary organic aerosols (SOA). In this study tailpipe exhaust of three typical in-use diesel vehicles under warm idling conditions was introduced directly into an indoor smog chamber with a 30m(3) Teflon reactor to characterize primary emissions and SOA formation during photo-oxidation. The emission factors of primary organic aerosol (POA) and black carbon (BC) for the three types of Chinese diesel vehicles ranged 0.18-0.91 and 0.15-0.51gkg-fuel(-1), respectively; and the SOA production factors ranged 0.50-1.8gkg-fuel(-1) and SOA/POA ratios ranged 0.7-3.7 with an average of 2.2. The fuel-based POA emission factors and SOA production factors from this study for idling diesel vehicle exhaust were 1-3 orders of magnitude higher than those reported in previous studies for idling gasoline vehicle exhaust. The emission factors for total particle numbers were 0.65-4.0×10(15)particleskg-fuel(-1), and particles with diameters less than 50nm dominated in total particle numbers. Traditional C2-C12 precursor non-methane hydrocarbons (NMHCs) could only explain less than 3% of the SOA formed during aging and contribution from other precursors including intermediate volatile organic compounds (IVOC) needs further investigation.

  12. High diversity of fungi in air particulate matter

    PubMed Central

    Fröhlich-Nowoisky, Janine; Pickersgill, Daniel A.; Després, Viviane R.; Pöschl, Ulrich

    2009-01-01

    Fungal spores can account for large proportions of air particulate matter, and they may potentially influence the hydrological cycle and climate as nuclei for water droplets and ice crystals in clouds, fog, and precipitation. Moreover, some fungi are major pathogens and allergens. The diversity of airborne fungi is, however, not well-known. By DNA analysis we found pronounced differences in the relative abundance and seasonal cycles of various groups of fungi in coarse and fine particulate matter, with more plant pathogens in the coarse fraction and more human pathogens and allergens in the respirable fine particle fraction (<3 μm). Moreover, the ratio of Basidiomycota to Ascomycota was found to be much higher than previously assumed, which might also apply to the biosphere. PMID:19617562

  13. SIZE DISTRIBUTION AND RATE OF PRODUCTION OF AIRBORNE PARTICULATE MATTER GENERATED DURING METAL CUTTING

    SciTech Connect

    M.A. Ebadian, Ph.D.; S.K. Dua, Ph.D., C.H.P.; Hillol Guha, Ph.D.

    2001-01-01

    During deactivation and decommissioning activities, thermal cutting tools, such as plasma torch, laser, and gasoline torch, are used to cut metals. These activities generate fumes, smoke and particulates. These airborne species of matter, called aerosols, may be inhaled if suitable respiratory protection is not used. Inhalation of the airborne metallic aerosols has been reported to cause ill health effects, such as acute respiratory syndrome and chromosome damage in lymphocytes. In the nuclear industry, metals may be contaminated with radioactive materials. Cutting these metals, as in size reduction of gloveboxes and tanks, produces high concentrations of airborne transuranic particles. Particles of the respirable size range (size < 10 {micro}m) deposit in various compartments of the respiratory tract, the fraction and the site in the respiratory tract depending on the size of the particles. The dose delivered to the respiratory tract depends on the size distribution of the airborne particulates (aerosols) and their concentration and radioactivity/toxicity. The concentration of airborne particulate matter in an environment is dependent upon the rate of their production and the ventilation rate. Thus, measuring aerosol size distribution and generation rate is important for (1) the assessment of inhalation exposures of workers, (2) the selection of respiratory protection equipment, and (3) the design of appropriate filtration systems. Size distribution of the aerosols generated during cutting of different metals by plasma torch was measured. Cutting rates of different metals, rate of generation of respirable mass, as well as the fraction of the released kerf that become respirable were determined. This report presents results of these studies. Measurements of the particles generated during cutting of metal plates with a plasma arc torch revealed the presence of particles with mass median aerodynamic diameters of particles close to 0.2 {micro}m, arising from

  14. Toward the next generation of air quality monitoring: Particulate Matter

    NASA Astrophysics Data System (ADS)

    Engel-Cox, Jill; Kim Oanh, Nguyen Thi; van Donkelaar, Aaron; Martin, Randall V.; Zell, Erica

    2013-12-01

    Fine particulate matter is one of the key global pollutants affecting human health. Satellite and ground-based monitoring technologies as well as chemical transport models have advanced significantly in the past 50 years, enabling improved understanding of the sources of fine particles, their chemical composition, and their effect on human and environmental health. The ability of air pollution to travel across country and geographic boundaries makes particulate matter a global problem. However, the variability in monitoring technologies and programs and poor data availability make global comparison difficult. This paper summarizes fine particle monitoring, models that integrate ground-based and satellite-based data, and communications, then recommends steps for policymakers and scientists to take to expand and improve local and global indicators of particulate matter air pollution. One of the key set of recommendations to improving global indicators is to improve data collection by basing particulate matter monitoring design and stakeholder communications on the individual country, its priorities, and its level of development, while at the same time creating global data standards for inter-country comparisons. When there are good national networks that produce consistent quality data that is shared openly, they serve as the foundation for better global understanding through data analysis, modeling, health impact studies, and communication. Additionally, new technologies and systems should be developed to expand personal air quality monitoring and participation of non-specialists in crowd-sourced data collections. Finally, support to the development and improvement of global multi-pollutant indicators of the health and economic effects of air pollution is essential to addressing improvement of air quality around the world.

  15. Organic content of particulate matter in turbine engine exhaust

    SciTech Connect

    Robertson, D.J.; Groth, R.H.; Blasko, T.J.

    1980-03-01

    Research report:Solid particulate matter, mainly carbon, emitted during fossil fuels combustion contains a variety of organic species adsorbed onto it. Studies were conducted to identify the organic compounds generated by a gas turbine engine. Total organics were determined by gas chromatography and flame ionization. Polynuclear aromatic hydrocarbons, phenols, and nitrosamines were present in samples collected from exhaust gases. (1 diagram, 4 references, 11 tables)

  16. Electrically heated particulate matter filter soot control system

    DOEpatents

    Gonze, Eugene V.; Paratore, Jr., Michael J.; Bhatia, Garima

    2016-03-15

    A regeneration system includes a particulate matter (PM) filter with an upstream end for receiving exhaust gas and a downstream end. A control module determines a current soot loading level of the PM filter and compares the current soot loading level to a predetermined soot loading level. The control module permits regeneration of the PM filter when the current soot loading level is less than the predetermined soot loading level.

  17. [Form of the particulate matter ambient air standards in China].

    PubMed

    Wang, Shuai; Ding, Jun-Nan; Wang, Rui-Bin; Li, Jian-Jun; Meng, Xiao-Yan; Yang, Bin; Lin, Hong

    2014-02-01

    Based on the principles from the World Health Organization (WHO) and the United States, an analysis was conducted to study the form of 24-hour standard of particulate matter in China by methods of statistical regression, proportional rollback and controlling contrast maps, using the monitoring data of inhalable particulate matter (PM10) from 120 cities in China during year 2005 to 2012. It was found that for cities in China, when the annual arithmetic mean of PM10 was equal to the national standard, the non-exceedance rates of daily average PM10 in most cities were higher than 95.0% , and the average rate for all cities was 97.1%. The average non-exceedance rate was 96.3% for cities in North China and Northwest China, 96.6% for Northeast China, 97.2% for East China and Central South China, and 98.1% for Southwest China. When the 97th percentile was chosen as the form of 24-hour standard of particulate matter for China, the 24-hour standard had an equal controlling strength with the annual standard. The 24-hour standard will become the controlling standard when larger percentiles were chosen, otherwise the contrary. By considering together the statistical characteristics of PM10 level in China, the robustness of the percentiles and protection of human health, the 95th percentile was suitable as the preferred form of the 24-hour standard of PM10 and PM2.5 in China.

  18. Total particulate matter concentration skews cigarette smoke's gene expression profile.

    PubMed

    Dvorkin-Gheva, Anna; Vanderstocken, Gilles; Yildirim, Ali Önder; Brandsma, Corry-Anke; Obeidat, Ma'en; Bossé, Yohan; Hassell, John A; Stampfli, Martin R

    2016-10-01

    Exposure of small animals to cigarette smoke is widely used as a model to study the pathogenesis of chronic obstructive pulmonary disease. However, protocols and exposure systems utilised vary substantially and it is unclear how these different systems compare. We analysed the gene expression profile of six publically available murine datasets from different cigarette smoke-exposure systems and related the gene signatures to three clinical cohorts. 234 genes significantly regulated by cigarette smoke in at least one model were used to construct a 55-gene network containing 17 clusters. Increasing numbers of differentially regulated clusters were associated with higher total particulate matter concentrations in the different datasets. Low total particulate matter-induced genes mainly related to xenobiotic/detoxification responses, while higher total particulate matter activated immune/inflammatory processes in addition to xenobiotic/detoxification responses. To translate these observations to the clinic, we analysed the regulation of the revealed network in three human cohorts. Similar to mice, we observed marked differences in the number of regulated clusters between the cohorts. These differences were not determined by pack-year. Although none of the experimental models exhibited a complete alignment with any of the human cohorts, some exposure systems showed higher resemblance. Thus, depending on the cohort, clinically observed changes in gene expression may be mirrored more closely by specific cigarette smoke exposure systems. This study emphasises the need for careful validation of animal models.

  19. Total particulate matter concentration skews cigarette smoke's gene expression profile

    PubMed Central

    Dvorkin-Gheva, Anna; Vanderstocken, Gilles; Yildirim, Ali Önder; Brandsma, Corry-Anke; Obeidat, Ma'en; Bossé, Yohan; Hassell, John A.

    2016-01-01

    Exposure of small animals to cigarette smoke is widely used as a model to study the pathogenesis of chronic obstructive pulmonary disease. However, protocols and exposure systems utilised vary substantially and it is unclear how these different systems compare. We analysed the gene expression profile of six publically available murine datasets from different cigarette smoke-exposure systems and related the gene signatures to three clinical cohorts. 234 genes significantly regulated by cigarette smoke in at least one model were used to construct a 55-gene network containing 17 clusters. Increasing numbers of differentially regulated clusters were associated with higher total particulate matter concentrations in the different datasets. Low total particulate matter-induced genes mainly related to xenobiotic/detoxification responses, while higher total particulate matter activated immune/inflammatory processes in addition to xenobiotic/detoxification responses. To translate these observations to the clinic, we analysed the regulation of the revealed network in three human cohorts. Similar to mice, we observed marked differences in the number of regulated clusters between the cohorts. These differences were not determined by pack-year. Although none of the experimental models exhibited a complete alignment with any of the human cohorts, some exposure systems showed higher resemblance. Thus, depending on the cohort, clinically observed changes in gene expression may be mirrored more closely by specific cigarette smoke exposure systems. This study emphasises the need for careful validation of animal models. PMID:27995131

  20. Effects of Crayfish on Quality of Fine Particulate Organic Matter

    NASA Astrophysics Data System (ADS)

    Montemarano, J. J.; Kershner, M. W.; Leff, L. G.

    2005-05-01

    The origin and ontogeny of detritus often determines its bioavailability. Crayfish shred and consume detrital organic matter, influencing fine particulate organic matter (FPOM) availability, composition and quality. Given consumption of FPOM by many invertebrates, crayfish can indirectly affect these organisms by altering FPOM bioavailability through organic matter fragmentation, biofilm disturbance, and defecation. These effects may or may not vary among coarse particulate organic matter (CPOM) from different leaf species. To assess crayfish effects on FPOM quality, crayfish were fed stream-conditioned maple or oak leaves in hanging 1-mm mesh-bottom baskets in aquaria. After 12 h, crayfish and remaining leaves were removed. FPOM fragments that fell through the mesh were vacuum filtered and analyzed for percent organic matter, C:N ratio, and bacterial abundance. The same analyses were conducted on crayfish feces collected using finger cots encasing crayfish abdomens. C:N ratios did not differ between feces and maple leaf CPOM, but were lower in FPOM produced through fragmentation and disturbance (P = 0.023). Overall, crayfish alter the ontogeny of detritus, which may, in turn, affect stream FPOM dynamics.

  1. Global Chemical Composition of Ambient Fine Particulate Matter for Exposure Assessment

    SciTech Connect

    Philip, Sajeev; Martin, Randall V.; van Donkelaar, Aaron; Lo, Jason Wai-Ho; Wang, Yuxuan; Chen, Dan; Zhang, Lin; Kasibhatla, Prasad S.; Wang, Siwen; Zhang, Qiang; Lu, Zifeng; Streets, David G.; Bittman, Shabtai; Macdonald, Douglas J.

    2014-10-24

    Epidemiologic and health impact studies are inhibited by the paucity of global, long-term measurements of the chemical composition of fine particulate matter. We inferred PM2.5 chemical composition at 0.1° × 0.1° spatial resolution for 2004–2008 by combining aerosol optical depth retrieved from the MODIS and MISR satellite instruments, with coincident profile and composition information from the GEOS-Chem global chemical transport model. Evaluation of the satellite-model PM2.5 composition data set with North American in situ measurements indicated significant spatial agreement for secondary inorganic aerosol, particulate organic mass, black carbon, mineral dust, and sea salt. We found that global population-weighted PM2.5 concentrations were dominated by particulate organic mass (11.9 ± 7.3 μg/m3), secondary inorganic aerosol (11.1 ± 5.0 μg/m3), and mineral dust (11.1 ± 7.9 μg/m3). Secondary inorganic PM2.5 concentrations exceeded 30 μg/m3 over East China. Sensitivity simulations suggested that population-weighted ambient PM2.5 from biofuel burning (11 μg/m3) could be almost as large as from fossil fuel combustion sources (17 μg/m3). In conclusion, these estimates offer information about global population exposure to the chemical components and sources of PM2.5.

  2. Particulate matter and manganese exposures in Toronto, Canada

    NASA Astrophysics Data System (ADS)

    Pellizzari, E. D.; Clayton, C. A.; Rodes, C. E.; Mason, R. E.; Piper, L. L.; Fort, B.; Pfeifer, G.; Lynam, D.

    Methylcyclopentadienyl manganese tricarbonyl (MMT) is a manganese-based gasoline additive used to enhance automobile performance. MMT has been used in Canadian gasoline for about 20 yr. Because of the potential for increased levels of Mn in particulate matter resulting from automotive exhausts, a large-scale population-based exposure study (˜1000 participant periods) was conducted in Toronto, Canada, to estimate the distribution of 3-day average personal exposures to particulate matter (PM 2.5 and PM 10) and Mn. A stratified, three-stage, two-phase probability, longitudinal sample design of the metropolitan population was employed. Residential indoor and outdoor, and ambient levels (at a fixed site and on a roof) of PM 2.5, PM 10, and Mn were also measured. Supplementary data on traffic counts, meteorology, MMT levels in gasoline, personal occupations, and activities (e.g. amount of vehicular usage) were collected. Overall precision (%RSD) for analysis of duplicate co-located samples ranged from 2.5 to 5.0% for particulate matter and 3.1 to 5.5% for Mn. The detection limits were 1.47 and 3.45 μg m -3 for the PM 10 and PM 2.5 fractions, respectively, and 5.50 and 1.83 ng m -3 for Mn in PM 10 and PM 2.5, respectively. These low detection limits permitted the reporting of concentrations for >98% of the samples. For PM 10, the personal particulate matter levels (median 48.5 μg m -3) were much higher than either indoor (23.1 μg m -3) or outdoor levels (23.6 μg m -3). The median levels for PM 2.5 for personal, indoor, and outdoor were 28.4, 15.4 and 13.2 μg m -3, respectively. The correlation between PM 2.5 personal exposures and indoor concentrations was high (0.79), while correlations between personal and the outdoor, fixed site and roof site were low (0.16-0.27). Indoor Mn concentration distributions (in PM 2.5 and PM 10), unlike particulate matter, exhibited much lower and less variable levels that the corresponding outdoor data. The median personal exposure

  3. Source apportionment studies on particulate matter in Beijing/China

    NASA Astrophysics Data System (ADS)

    Suppan, P.; Shen, R.; Shao, L.; Schrader, S.; Schäfer, K.; Norra, S.; Vogel, B.; Cen, K.; Wang, Y.

    2013-05-01

    More than 15 million people in the greater area of Beijing are still suffering from severe air pollution levels caused by sources within the city itself but also from external impacts like severe dust storms and long range advection from the southern and central part of China. Within this context particulate matter (PM) is the major air pollutant in the greater area of Beijing (Garland et al., 2009). PM did not serve only as lead substance for air quality levels and therefore for adverse health impact effects but also for a strong influence on the climate system by changing e.g. the radiative balance. Investigations on emission reductions during the Olympic Summer Games in 2008 have caused a strong reduction on coarser particles (PM10) but not on smaller particles (PM2.5). In order to discriminate the composition of the particulate matter levels, the different behavior of coarser and smaller particles investigations on source attribution, particle characteristics and external impacts on the PM levels of the city of Beijing by measurements and modeling are performed: a) Examples of long term measurements of PM2.5 filter sampling in 2010/2011 with the objectives of detailed chemical (source attribution, carbon fraction, organic speciation and inorganic composition) and isotopic analyses as well as toxicological assessment in cooperation with several institutions (Karlsruhe Institute of Technology (IfGG/IMG), Helmholtz Zentrum München (HMGU), University Rostock (UR), Chinese University of Mining and Technology Beijing, CUMTB) will be discussed. b) The impact of dust storm events on the overall pollution level of particulate matter in the greater area of Beijing is being assessed by the online coupled comprehensive model system COSMO-ART. First results of the dust storm modeling in northern China (2011, April 30th) demonstrates very well the general behavior of the meteorological parameters temperature and humidity as well as a good agreement between modeled and

  4. STATISTICAL ISSUES IN THE STUDY OF AIR POLLUTION INVOLVING AIRBORNE PARTICULATE MATTER

    EPA Science Inventory

    Epidemiological research in the early 1990s focusing on health effects of airborne particulate matter pointed to a statistical association between increases in concentration of particulate in ambient air and increases in daily nonaccidental mortality, particularly among the eld...

  5. Continuous and semicontinuous monitoring techniques for particulate matter mass and chemical components: a synthesis of findings from EPA's Particulate Matter Supersites Program and related studies.

    PubMed

    Solomon, Paul A; Sioutas, Constantinos

    2008-02-01

    The U.S. Environmental Protection Agency (EPA) established the Particulate Matter (PM) Supersites Program to provide key stakeholders (government and private sector) with significantly improved information needed to develop effective and efficient strategies for reducing PM on urban and regional scales. All Supersites projects developed and evaluated methods and instruments, and significant advances have been made and applied within these programs to yield new insights to our understanding of PM accumulation in air as well as improved source-receptor relationships. The tested methods include a variety of continuous and semicontinuous instruments typically with a time resolution of an hour or less. These methods often overcome many of the limitations associated with measuring atmospheric PM mass concentrations by daily filter-based methods (e.g., potential positive or negative sampling artifacts). Semicontinuous coarse and ultrafine mass measurement methods also were developed and evaluated. Other semicontinuous monitors tested measured the major components of PM such as nitrate, sulfate, ammonium, organic and elemental carbon, trace elements, and water content of the aerosol as well as methods for other physical properties of PM, such as number concentration, size distribution, and particle density. Particle mass spectrometers, although unlikely to be used in national routine monitoring networks in the foreseeable future because of their complex technical requirements and cost, are mentioned here because of the wealth of new information they provide on the size-resolved chemical composition of atmospheric particles on a near continuous basis. Particle mass spectrometers likely represent the greatest advancement in PM measurement technology during the last decade. The improvements in time resolution achieved by the reported semicontinuous methods have proven to be especially useful in characterizing ambient PM, and are becoming essential in allowing scientists to

  6. Evolution of ozone, particulates, and aerosol direct radiative forcing in the vicinity of Houston using a fully coupled meteorology-chemistry-aerosol model

    NASA Astrophysics Data System (ADS)

    Fast, Jerome D.; Gustafson, William I.; Easter, Richard C.; Zaveri, Rahul A.; Barnard, James C.; Chapman, Elaine G.; Grell, Georg A.; Peckham, Steven E.

    2006-11-01

    A new fully coupled meteorology-chemistry-aerosol model is used to simulate the urban- to regional-scale variations in trace gases, particulates, and aerosol direct radiative forcing in the vicinity of Houston over a 5 day summer period. Model performance is evaluated using a wide range of meteorological, chemistry, and particulate measurements obtained during the 2000 Texas Air Quality Study. The predicted trace gas and particulate distributions were qualitatively similar to the surface and aircraft measurements with considerable spatial variations resulting from urban, power plant, and industrial sources of primary pollutants. Sulfate, organic carbon, and other inorganics were the largest constituents of the predicted particulates. The predicted shortwave radiation was 30 to 40 W m-2 closer to the observations when the aerosol optical properties were incorporated into the shortwave radiation scheme; however, the predicted hourly aerosol radiative forcing was still underestimated by 10 to 50 W m-2. The predicted aerosol radiative forcing was larger over Houston and the industrial ship channel than over the rural areas, consistent with surface measurements. The differences between the observed and simulated aerosol radiative forcing resulted from transport errors, relative humidity errors in the upper convective boundary layer that affect aerosol water content, secondary organic aerosols that were not yet included in the model, and uncertainties in the primary particulate emission rates. The current model was run in a predictive mode and demonstrates the challenges of accurately simulating all of the meteorological, chemical, and aerosol parameters over urban to regional scales that can affect aerosol radiative forcing.

  7. Chemical Characterization and Source Apportionment of Particulate Matter in Lahore, Pakistan

    NASA Astrophysics Data System (ADS)

    von Schneidemesser, Erika; Stone, Elizabeth; Quraishi, Tauseef; Schauer, James; Shafer, Martin; Mahmood, Abid

    2010-05-01

    Lahore, Pakistan is a rapidly growing megacity with a population approaching 10 million. A significant issue affecting many of the world's megacities is extremely high levels of air pollution associated with transportation, solid fuel combustion, and industrial sources. High ambient concentrations of particulate matter (PM), as well as high levels of toxic components of PM, have been linked to increased mortality and morbidity. Although much focus has been directed at particulate matter mass, in many developing and underdeveloped nations, the adverse health impacts of high levels of PM are further enhanced by the high concentrations of toxic components in PM. To address these issues is Lahore, a measurement campaign of fine (PM2.5) and coarse (PM10-2.5) particulate matter was conducted for the 2007 calendar year, which included measurements of particle mass, detailed chemical composition of PM and source apportionment calculations. Annual average PM2.5 and PM10 concentrations were measured to be 194 µg m-3 and 336 µg m-3, respectively, with daily 24-hour maximum concentrations of 410 µg m-3 and 650 µg m-3 for PM2.5 and PM10, respectively. PM2.5 and PM10 samples were analysed for organic and elemental carbon, organic species, ionic species, elemental composition, water soluble elements and biological activity using a macrophage ROS assay. The coarse mode was dominated by crustal dust components, while the fine fraction was dominated by carbonaceous aerosols. The PM10 elemental composition data, which included data for toxic metals, was processed using principle component analysis to determine likely source categories. Seven factors were identified explaining 91% of the variance of the measured components. The factors included a number of industrial sources, re-suspended soil, mobile sources, and regional secondary aerosol. Source contributions to the organic carbon (OC) component of the PM2.5 fraction were identified using organic tracer species and chemical

  8. Particulate matter air quality assessment over southeast United States using satellite and ground measurements

    NASA Astrophysics Data System (ADS)

    Gupta, Pawan

    Fine particles (PM2.5, particles with aerodynamic diameter less than 2.5 mum) can penetrate deep inside the human lungs and recent scientific studies have shown thousands of deaths occur each year around the world, prematurely, due to a high concentration of particulate matter. Therefore, monitoring and forecasting of surface level fine particulate matter air quality is very important. Typically air quality measurements are made from ground stations. In recent years, linear regression relationships between satellite derived aerosol optical thickness (AOT) and surface measured PM2.5 mass concentration are formed and used to estimate PM2.5 in the areas where surface measurements are not available. This type of simple linear relationships varies with regions and seasons, and does not provide accurate enough estimation of surface level pollution and many studies have shown that AOT alone is not sufficient for PM2.5 mass concentration estimations. Furthermore, AOT represents aerosol loading in the entire column of the atmosphere whereas PM2.5 is measured at the surface; hence, the knowledge of vertical distribution of aerosols coupled with meteorology becomes critical in PM2.5 estimations. In this dissertation I used three years (2004-2006) of coincident hourly PM2.5, MODerate resolution Imaging Spectroradiometer (MODIS) derived AOT, and Rapid Update Cycle (RUC) analyzed meteorological fields to assess PM2.5 air quality in the Southeast United States. I explored the use of two-variate (TVM), multi-variate (MVM) and artificial neural network (ANN) methods for estimating PM2.5 over 85 stations in the region. First, satellite data were analyzed for sampling biases, quality, and impact of clouds. Results show that MODIS-Terra AOT data was available only about 50% of the days in any given month due to cloud over and unfavorable surface conditions, but this produced a sampling bias of less than 2 mugm-3. Results indicate that there is up to three fold improvements in the

  9. Chemical characterisation of total suspended particulate matter from a remote area in Amazonia

    NASA Astrophysics Data System (ADS)

    Gonçalves, Cátia; Figueiredo, Bernardino R.; Alves, Célia A.; Cardoso, Arnaldo A.; da Silva, Rodrigo; Kanzawa, Simone H.; Vicente, Ana Margarida

    2016-12-01

    This research had as study object the total suspended particulate matter collected in the Alenquer region, a remote area in the Pará state. The main objectives were the characterisation of the inorganic and organic chemical composition of the aerosol, looking for seasonal patterns and the identification of probable emission sources and formation processes. A set of 30 samples were collected in the rainy (April-May) and dry season (August-September) of 2014. The analytical methods included gravimetric analysis, water-soluble ions analysis by ion chromatography (IC), elemental analysis by inductively coupled plasma mass spectrometry (ICP-MS) equipped with collision cell technology, carbonaceous content determination with a thermal-optical system and organic speciation by gas chromatography-mass spectrometry (GC-MS). The average concentrations of particulate matter ranged from 14 ± 1.3 μg·m- 3 to 31 ± 7.8 μg·m- 3, in the rainy and dry season, respectively. The carbonaceous content represented, on average, approximately 27% and 21% of the particulate matter in the rainy and dry season, respectively. Na+, Cl-, SO₄2 -, and NO₃- yield the highest concentrations in both seasons. Na was the dominant element, reflecting the transport of air masses from the Atlantic. An increase in concentrations between the rainy and dry seasons was especially noted for the terrigenous elements such Mn, Fe and Al. The chromatographically resolved organics included n-alkanes, n-alkenes, PAHs, n-alkanoic acids, n-di-acids, resin acids and some phenolic compounds. The primary inputs of organic constituents to the aerosols of Alenquer based on the homologous compound series and biomarkers were: (i) natural emissions from terrestrial higher plants waxes, particularly in dry season; (ii) anthropogenic emissions from diesel fuel combustion and biomass combustion, predominating during the dry season. The chemical characterisation along with the backward trajectory cluster analysis

  10. Removal of Particulate Matter Emissions from a Vehicle Using a Self-Powered Triboelectric Filter.

    PubMed

    Han, Chang Bao; Jiang, Tao; Zhang, Chi; Li, Xiaohui; Zhang, Chaoying; Cao, Xia; Wang, Zhong Lin

    2015-12-22

    Particulate matter (PM) pollution from automobile exhaust has become one of the main pollution sources in urban environments. Although the diesel particulate filter has been used in heavy diesel vehicles, there is no particulate filter for most gasoline cars or light-duty vehicles because of high cost. Here, we introduce a self-powered triboelectric filter for removing PMs from automobile exhaust fumes using the triboelectrification effect. The finite element simulation reveals that the collision or friction between PTFE pellets and electrodes can generate large triboelectric charges and form a space electric field as high as 12 MV/m, accompanying an open-circuit voltage of ∼6 kV between the two electrodes, which is comparable to the measured value of 3 kV. By controlling the vibration frequency and fill ratio of pellets, more than 94% PMs in aerosol can be removed using the high electric field in the triboelectric filter. In real automobile exhaust fumes, the triboelectic filter has a mass collection efficiency of ∼95.5% for PM2.5 using self-vibration of the tailpipe.

  11. Origin of fine carbonaceous particulate matter in the Western Mediterranean Basin: fossil versus modern sources

    NASA Astrophysics Data System (ADS)

    Cruz Minguillón, María.; Perron, Nolwenn; Querol, Xavier; Szidat, Sönke; Fahrni, Simon; Wacker, Lukas; Reche, Cristina; Cusack, Michael; Baltensperger, Urs; Prévôt, André S. H.

    2010-05-01

    The present work was carried out in the frame of the international field campaign DAURE (Determination of the sources of atmospheric Aerosols in Urban and Rural Environments in the western Mediterranean). The objective of this campaign is to study the aerosol pollution episodes occurring at regional scale during winter and summer in the Western Mediterranean Basin. As part of this campaign, this work focuses on identifying the origin of fine carbonaceous aerosols. To this end, fine particulate matter (PM1) samples were collected during two different seasons (February-March and July 2009) at two sites: an urban site (Barcelona, NE Spain) and a rural European Supersite for Atmospheric Aerosol Research (Montseny, NE Spain). Subsequently, 14C analyses were carried out on these samples, both in the elemental carbon (EC) fraction and the organic carbon (OC) fraction, in order to distinguish between modern carbonaceous sources (biogenic emissions and biomass burning emissions) and fossil carbonaceous sources (mainly road traffic). Preliminary results from the winter period show that 40% of the OC at Barcelona has a fossil origin whereas at Montseny this percentage is 30%. These values can be considered as unexpected given the nature of the sites. Nevertheless, the absolute concentrations of fossil OC at Barcelona and Montseny differ by a factor of 2 (the first being higher), since the total OC at Montseny is lower than at Barcelona. Further evaluation of results and comparison with other measurements carried out during the campaign are required to better evaluate the origin of the fine carbonaceous matter in the Western Mediterranean Basin. Acknowledgements: Spanish Ministry of Education and Science, for a Postdoctoral Grant awarded to M.C. Minguillón in the frame of Programa Nacional de Movilidad de Recursos Humanos del Plan nacional de I-D+I 2008-2011. Spanish Ministry of Education and Science, for the Acción Complementaria DAURE CGL2007-30502-E/CLI.

  12. Impact assessment of respirable suspended particulate matter from diesel generator sets used for pumping station.

    PubMed

    Talwar, B; Pipalatkar, P; Gajghate, D G; Nema, P

    2010-10-01

    Prediction of respirable suspended particulate matter impacts of diesel generator sets used for pumping station has been made using meteorological data, information on stack characteristics and emission rate, baseline ambient particulate matter and Industrial Source Complex Short Term (ISCST-3) model. It is observed that particulate matter emission from pumping station-S workplace diesel generator sets ranged from 2.4 to 436.5 mg Nm⁻³ and while at pumping station-C, it ranged from 23.2 to 186.5 mg Nm⁻³. The predicted and ambient respirable suspended particulate matter concentrations are below the national air quality standard for respirable suspended particulate matter in a mixed industrial area. Metals contents in respirable suspended particulate matter indicate the origin of crustal and mobile sources. Therefore, the impact of diesel generator sets used for pumping of crude oil on local air quality would be acceptable.

  13. Wireless zoned particulate matter filter regeneration control system

    DOEpatents

    Gonze, Eugene V [Pinckney, MI; Kirby, Kevin W [Calabasas Hills, CA; Phelps, Amanda [Malibu, CA

    2011-10-04

    An assembly includes a particulate matter (PM) filter that comprises an upstream end for receiving exhaust gas, a downstream end and multiple zones. An absorbing layer absorbs microwave energy in one of N frequency ranges and is arranged with the upstream end. N is an integer. A frequency selective filter has M frequency selective segments and receives microwave energy in the N frequency ranges. M is an integer. One of the M frequency selective segments permits passage of the microwave energy in one of the N frequency ranges and does not permit passage of microwave energy in the other of the N frequency ranges.

  14. Apparatus for removal of particulate matter from gas streams

    DOEpatents

    Smith, Peyton L.; Morse, John C.

    2000-01-01

    An apparatus for the removal of particulate matter from the gaseous product stream of an entrained flow coal gasifier which apparatus includes an initial screen, an intermediate screen which is aligned with the direction of flow of the gaseous product stream and a final screen transversely disposed to the flow of gaseous product and which apparatus is capable of withstanding at least a pressure differential of about 10 psi (68.95 kPa) or greater at the temperatures of the gaseous product stream.

  15. AIR QUALITY: MERCURY, TRACE ELEMENTS, AND PARTICULATE MATTER CONFERENCE

    SciTech Connect

    John H. Pavlish; Steven A. Benson

    1999-07-01

    This final report summarizes the planning/preparation, facilitation, and outcome of the conference entitled ''Air Quality: Mercury, Trace Elements, and Particulate Matter'' that was held December 1-4, 1998, in McLean, Virginia (on the outskirts of Washington, DC). The goal of the conference was to bring together industry, government, and the research community to discuss the critical issue of how air quality can impact human health and the ecosystem, specifically hazardous air pollutants and fine airborne particles; available and developing control technologies; strategies and research needs; and an update on federal and state policy and regulations, related implementation issues, and the framework of the future.

  16. Ash reduction system using electrically heated particulate matter filter

    DOEpatents

    Gonze, Eugene V [Pinckney, MI; Paratore, Jr., Michael J; He, Yongsheng [Sterling Heights, MI

    2011-08-16

    A control system for reducing ash comprises a temperature estimator module that estimates a temperature of an electrically heated particulate matter (PM) filter. A temperature and position estimator module estimates a position and temperature of an oxidation wave within the electrically heated PM filter. An ash reduction control module adjusts at least one of exhaust flow, fuel and oxygen levels in the electrically heated PM filter to adjust a position of the oxidation wave within the electrically heated PM filter based on the oxidation wave temperature and position.

  17. Low exhaust temperature electrically heated particulate matter filter system

    DOEpatents

    Gonze, Eugene V [Pinckney, MI; Paratore, Jr., Michael J.; Bhatia, Garima [Bangalore, IN

    2012-02-14

    A system includes a particulate matter (PM) filter, a sensor, a heating element, and a control module. The PM filter includes with an upstream end that receives exhaust gas, a downstream end and multiple zones. The sensor detects a temperature of the exhaust gas. The control module controls current to the heating element to convection heat one of the zones and initiate a regeneration process. The control module selectively increases current to the heating element relative to a reference regeneration current level when the temperature is less than a predetermined temperature.

  18. Elevated exhaust temperature, zoned, electrically-heated particulate matter filter

    DOEpatents

    Gonze, Eugene V [Pinckney, MI; Bhatia, Garima [Bangalore, IN

    2012-04-17

    A system includes an electrical heater and a particulate matter (PM) filter that is arranged one of adjacent to and in contact with the electrical heater. A control module selectively increases an exhaust gas temperature of an engine to a first temperature and that initiates regeneration of the PM filter using the electrical heater while the exhaust gas temperature is above the first temperature. The first temperature is greater than a maximum exhaust gas temperature at the PM filter during non-regeneration operation and is less than an oxidation temperature of the PM.

  19. Fe, Ni and Zn speciation, in airborne particulate matter

    NASA Astrophysics Data System (ADS)

    Thiodjio Sendja, Bridinette; Aquilanti, Giuliana; Vassura, Ivano; Giorgetti, Marco

    2016-05-01

    The study of elemental speciation in atmospheric particulate matter is important for the assessment of the source of the particle as well for the evaluation of its toxicity. XANES data at Fe, Ni, and Zn K-edges are recorded on a sample of urban dust (from the Rimini area of Emilia Romagna region, Italy) deposited on a filter and on the NIST standard reference material 1648. Using linear combination fitting we give an indication of the chemical species of the three metals present in the samples.

  20. Fine particulate matter and visibility in the Lake Tahoe Basin: chemical characterization, trends, and source apportionment.

    PubMed

    Green, Mark C; Chen, L W Antony; DuBois, David W; Molenar, John V

    2012-08-01

    Speciated PM2.5 (particulate matter with an aerodynamic diameteraerosol dominated reconstructedfine mass at both sites, with 58% at Bliss State Park (BLIS) and 68% at South Lake Tahoe (SOLA). Fine mass at SOLA is 2.5 times that at BLIS, mainly due to enhanced organic and elemental carbon (OC and EC). SOLA experiences a winter peak in PM25 mainly due to OC and EC from residential wood combustion, whereas BLIS experiences a summer peak in PM2.5 mainly due to OC and ECfrom wildfires. Carbonaceous aerosol dominates visibility impairment, causing about 1/2 the reconstructed aerosol light extinction at BLIS and 70% at SOLA. Trend analysis (1990-2009) showed statistically significant decreases in aerosol extinction at BLIS on 20% best and 60% middle visibility days and statistically insignificant upward trends on 20% worst days. SOLA (1990-2003) showed statistically significant decreases in aerosol extinction for all day categories, driven by decreasing OC and EC. From the regional haze rule baseline period of 2000-2004 until 2005-2009, BLIS saw 20% best days improving and 20% worst days getting worse due to increased wildfire effects. Receptor modeling was performed using positive matrix factorization (PMF) and chemical mass balance (CMB). It confirmed that (1) biomass burning dominanted PM25 sources at both sites with increasing importance over time; (2) low combustion efficiency burning accounts for most of the biomass burning contribution; (3) road dust and traffic contributions were much higher at SOLA than at BLIS; and (4) industrial combustion and salting were minor sources.

  1. Spatiotemporal prediction of fine particulate matter during the 2008 northern California wildfires using machine learning.

    PubMed

    Reid, Colleen E; Jerrett, Michael; Petersen, Maya L; Pfister, Gabriele G; Morefield, Philip E; Tager, Ira B; Raffuse, Sean M; Balmes, John R

    2015-03-17

    Estimating population exposure to particulate matter during wildfires can be difficult because of insufficient monitoring data to capture the spatiotemporal variability of smoke plumes. Chemical transport models (CTMs) and satellite retrievals provide spatiotemporal data that may be useful in predicting PM2.5 during wildfires. We estimated PM2.5 concentrations during the 2008 northern California wildfires using 10-fold cross-validation (CV) to select an optimal prediction model from a set of 11 statistical algorithms and 29 predictor variables. The variables included CTM output, three measures of satellite aerosol optical depth, distance to the nearest fires, meteorological data, and land use, traffic, spatial location, and temporal characteristics. The generalized boosting model (GBM) with 29 predictor variables had the lowest CV root mean squared error and a CV-R2 of 0.803. The most important predictor variable was the Geostationary Operational Environmental Satellite Aerosol/Smoke Product (GASP) Aerosol Optical Depth (AOD), followed by the CTM output and distance to the nearest fire cluster. Parsimonious models with various combinations of fewer variables also predicted PM2.5 well. Using machine learning algorithms to combine spatiotemporal data from satellites and CTMs can reliably predict PM2.5 concentrations during a major wildfire event.

  2. Novel Collection and Toxicological Analysis Techniques for IC Engine Exhaust Particulate Matter

    SciTech Connect

    Michael Keane; Xiao-Chun Shi; Tong-man Ong

    2008-09-30

    The project staff partnered with Costas Sioutas from the University of Southern California to apply the VACES (Versatile Aerosol Concentration Enhancement System) to a diesel engine test facility at West Virginia University Department of Mechanical Engineering and later the NIOSH Lake Lynn Mine facility. The VACES system was able to allow diesel exhaust particulate matter (DPM) to grow to sufficient particle size to be efficiently collected with the SKC Biosampler impinger device, directly into a suspension of simulated pulmonary surfactant. At the WVU-MAE facility, the concentration of the aerosol was too high to allow efficient use of the VACES concentration enhancement, although aerosol collection was successful. Collection at the LLL was excellent with the diluted exhaust stream. In excess of 50 samples were collected at the LLL facility, along with matching filter samples, at multiple engine speed and load conditions. Replicate samples were combined and concentration increased using a centrifugal concentrator. Bioassays were negative for all tested samples, but this is believed to be due to insufficient concentration in the final assay suspensions.

  3. Evaluation of the Pulmonary Toxicity of Ambient Particulate Matter from Camp Victory, Iraq

    DTIC Science & Technology

    2015-01-01

    online DOI: 10.1080/15287394.2015.1072611 EVALUATION OF THE PULMONARY TOXICITY OF AMBIENT PARTICULATE MATTER FROM CAMP VICTORY, IRAQ K. L. Porter1, F. H. Y...studied. The relative toxicity of Camp Victory dust was evaluated by comparing it to particulate matter from northern Kuwait, a standard U.S. urban...the ubiquitous ambient particulate matter (PM). Airborne PM concentrations in SWA exceed environmental, occupational, and military exposure guidelines

  4. Characterization and Cytotoxic Assessment of Ballistic Aerosol Particulates for Tungsten Alloy Penetrators into Steel Target Plates

    PubMed Central

    Machado, Brenda I.; Murr, Lawrence E.; Suro, Raquel M.; Gaytan, Sara M.; Ramirez, Diana A.; Garza, Kristine M.; Schuster, Brian E.

    2010-01-01

    The nature and constituents of ballistic aerosol created by kinetic energy penetrator rods of tungsten heavy alloys (W-Fe-Ni and W-Fe-Co) perforating steel target plates was characterized by scanning and transmission electron microscopy. These aerosol regimes, which can occur in closed, armored military vehicle penetration, are of concern for potential health effects, especially as a consequence of being inhaled. In a controlled volume containing 10 equispaced steel target plates, particulates were systematically collected onto special filters. Filter collections were examined by scanning and transmission electron microscopy (SEM and TEM) which included energy-dispersive (X-ray) spectrometry (EDS). Dark-field TEM identified a significant nanoparticle concentration while EDS in the SEM identified the propensity of mass fraction particulates to consist of Fe and FeO, representing target erosion and formation of an accumulating debris field. Direct exposure of human epithelial cells (A549), a model for lung tissue, to particulates (especially nanoparticulates) collected on individual filters demonstrated induction of rapid and global cell death to the extent that production of inflammatory cytokines was entirely inhibited. These observations along with comparisons of a wide range of other nanoparticulate species exhibiting cell death in A549 culture may suggest severe human toxicity potential for inhaled ballistic aerosol, but the complexity of the aerosol (particulate) mix has not yet allowed any particular chemical composition to be identified. PMID:20948926

  5. Characterization and cytotoxic assessment of ballistic aerosol particulates for tungsten alloy penetrators into steel target plates.

    PubMed

    Machado, Brenda I; Murr, Lawrence E; Suro, Raquel M; Gaytan, Sara M; Ramirez, Diana A; Garza, Kristine M; Schuster, Brian E

    2010-09-01

    The nature and constituents of ballistic aerosol created by kinetic energy penetrator rods of tungsten heavy alloys (W-Fe-Ni and W-Fe-Co) perforating steel target plates was characterized by scanning and transmission electron microscopy. These aerosol regimes, which can occur in closed, armored military vehicle penetration, are of concern for potential health effects, especially as a consequence of being inhaled. In a controlled volume containing 10 equispaced steel target plates, particulates were systematically collected onto special filters. Filter collections were examined by scanning and transmission electron microscopy (SEM and TEM) which included energy-dispersive (X-ray) spectrometry (EDS). Dark-field TEM identified a significant nanoparticle concentration while EDS in the SEM identified the propensity of mass fraction particulates to consist of Fe and FeO, representing target erosion and formation of an accumulating debris field. Direct exposure of human epithelial cells (A549), a model for lung tissue, to particulates (especially nanoparticulates) collected on individual filters demonstrated induction of rapid and global cell death to the extent that production of inflammatory cytokines was entirely inhibited. These observations along with comparisons of a wide range of other nanoparticulate species exhibiting cell death in A549 culture may suggest severe human toxicity potential for inhaled ballistic aerosol, but the complexity of the aerosol (particulate) mix has not yet allowed any particular chemical composition to be identified.

  6. Characterization of particulate matter from diesel passenger cars tested on chassis dynamometers.

    PubMed

    Jung, Sungwoon; Lim, Jaehyun; Kwon, Sangil; Jeon, Sangwoo; Kim, Jeongsoo; Lee, Jongtae; Kim, Sunmoon

    2017-04-01

    Emission characterization of particle number as well as particle mass from three diesel passenger cars equipped with diesel particulate filter (DPF), diesel oxidation catalyst (DOC) and exhaust gas recirculation (EGR) under the vehicle driving cycles and regulatory cycle. Total particle number emissions (PNEs) decreased gradually during speed-up of vehicle from 17.3 to 97.3km/hr. As the average vehicle speed increases, the size-segregated peak of particle number concentration shifts to smaller size ranges of particles. The correlation analysis with various particulate components such as particle number concentration (PNC), ultrafine particle number concentration (UFPNC) and particulate matter (PM) mass was conducted to compare gaseous compounds (CO, CO2, HC and NOx). The UFPNC and PM were not only emitted highly in Seoul during severe traffic jam conditions, but also have good correlation with hydrocarbons and NOx influencing high potential on secondary aerosol generation. The effect of the dilution temperature on total PNC under the New European Driving Cycle (NEDC), was slightly higher than the dilution ratio. In addition, the nuclei mode (DP: ≤13nm) was confirmed to be more sensitive to the dilution temperature rather than other particle size ranges. Comparison with particle composition between vehicle speed cycles and regulatory cycle showed that sulfate was slightly increased at regulatory cycle, while other components were relatively similar. During cold start test, semivolatile nucleation particles were increased due to effect of cold environment. Research on particle formation dependent on dilution conditions of diesel passenger cars under the NEDC is important to verify impact on vehicular traffic and secondary aerosol formation in Seoul.

  7. Road tunnel, roadside, and urban background measurements of aliphatic compounds in size-segregated particulate matter

    NASA Astrophysics Data System (ADS)

    Alves, Célia A.; Oliveira, César; Martins, Natércia; Mirante, Fátima; Caseiro, Alexandre; Pio, Casimiro; Matos, Manuel; Silva, Hugo F.; Oliveira, Cristina; Camões, Filomena

    2016-02-01

    Particulate matter samples were collected in a road tunnel in Lisbon (PM0.5, PM0.5-1, PM1-2.5, and PM2.5-10) and at two urban locations representing roadside and background stations (PM2.5 and PM2.5-10). Samples were analysed for organic and elemental carbon (OC and EC), n-alkanes, n-alkenes, hopanes, some isoprenoid compounds, and steranes. Particulate matter concentrations in the tunnel were 17-31 times higher than at roadside in the vicinity, evidencing an aerosol origin almost exclusively in fresh vehicle emissions. PM0.5 in the tunnel comprised more than 60% and 80% of the total OC and EC mass in PM10, respectively. Concentrations of the different aliphatic groups of compounds in the tunnel were up to 89 times higher than at roadside and 143 times higher than at urban background. Based on the application of hopane-to-OC or hopanes-to-EC ratios obtained in the tunnel, it was found that vehicle emissions are the dominant contributor to carbonaceous particles in the city but do not represent the only source of these triterpenic compounds. Contrary to what has been observed in other studies, the Σhopane-to-EC ratios were higher in summer than in winter, suggesting that other factors (e.g. biomass burning, dust resuspension, and different fuels/engine technologies) prevail in relation to the photochemical decay of triterpenoid hydrocarbons from vehicle exhaust.

  8. Analysis of semi-volatile materials (SVM) in fine particulate matter

    NASA Astrophysics Data System (ADS)

    Salvador, Christian Mark; Chou, Charles C.-K.

    2014-10-01

    The mass fraction of semi-volatile materials (SVM) in fine particulate matter (PM2.5) was investigated at a subtropical urban aerosol observatory (TARO, 25.0 °N, 121.5 °E) in Taipei, Taiwan during August 2013. In particular, an integrated Denuder-FDMS-TEOM system was employed to study the effectiveness of the coupling of FDMS and TEOM instruments. The charcoal and MgO denuders used in this study performed a removal efficiency of 89 and 95% for positive interferences in OC and nitrate measurements, respectively, and did not induce a significant particle loss during the field campaign, suggesting that denuders should be considered as a standard device in PM2.5 instrumentation. Analysis on the mass concentration and speciation data found that, as a result of SVM loss, FRM-based measurement underestimated PM2.5 by 21% in our case. Coupling FDMS to TEOM significantly improved the bias in PM2.5 mass concentration from -25% to -14%. The negative bias in FDMS-TEOM was attributed to the failure of FDMS in recovering the mass of lost SVOMs in PM2.5. The results of this study highlight the significance of SVM in a subtropical urban environment, give a warning of underestimated health risk relevant to PM2.5 exposure, and necessitate further development of instrument and/or technique to provide accurate ambient levels of fine particulate matters.

  9. Satellite constraints on surface concentrations of particulate matter

    NASA Astrophysics Data System (ADS)

    Ford Hotmann, Bonne

    Because of the increasing evidence of the widespread adverse effects on human health from exposure to poor air quality and the recommendations of the World Health Organization to significantly reduce PM2.5 in order to reduce these risks, better estimates of surface air quality globally are required. However, surface measurements useful for monitoring particulate exposure are scarce, especially in developing countries which often experience the worst air pollution. Therefore, other methods are necessary to augment estimates in regions with limited surface observations. The prospect of using satellite observations to infer surface air quality is attractive; however, it requires knowledge of the complicated relationship between satellite-observed aerosol optical depth (AOD) and surface concentrations. This dissertation explores how satellite observations can be used in conjunction with a chemical transport model (GEOS-Chem) to better understand this relationship. First, we investigate the seasonality in aerosols over the Southeastern United States using observations from several satellite instruments (MODIS, MISR, CALIOP) and surface network sites (IMPROVE, SEARCH, AERONET). We find that the strong summertime enhancement in satellite-observed aerosol optical depth (factor 2-3 enhancement over wintertime AOD) is not present in surface mass concentrations (25-55% summertime enhancement). Goldstein et al. [2009] previously attributed this seasonality in AOD to biogenic organic aerosol; however, surface observations show that organic aerosol only accounts for ~35% of PM2.5 mass and exhibits similar seasonality to total surface PM2.5. The GEOS-Chem model generally reproduces these surface aerosol measurements, but under represents the AOD seasonality observed by satellites. We show that seasonal differences in water uptake cannot sufficiently explain the magnitude of AOD increase. As CALIOP profiles indicate the presence of additional aerosol in the lower troposphere

  10. Modeling particulate matter emissions during mineral loading process under weak wind simulation.

    PubMed

    Zhang, Xiaochun; Chen, Weiping; Ma, Chun; Zhan, Shuifen

    2013-04-01

    The quantification of particulate matter emissions from mineral handling is an important problem for the quantification of global emissions on industrial sites. Mineral particulate matter emissions could adversely impact environmental quality in mining regions, transport regions, and even on a global scale. Mineral loading is an important process contributing to mineral particulate matter emissions, especially under weak wind conditions. Mathematical models are effective ways to evaluate particulate matter emissions during the mineral loading process. The currently used empirical models based on the form of a power function do not predict particulate matter emissions accurately under weak wind conditions. At low particulate matter emissions, the models overestimated, and at high particulate matter emissions, the models underestimated emission factors. We conducted wind tunnel experiments to evaluate the particulate matter emission factors for the mineral loading process. A new approach based on the mathematical form of a logistical function was developed and tested. It provided a realistic depiction of the particulate matter emissions during the mineral loading process, accounting for fractions of fine mineral particles, dropping height, and wind velocity.

  11. Satellite-based retrieval of particulate matter concentrations over the United Arab Emirates (UAE)

    NASA Astrophysics Data System (ADS)

    Zhao, Jun; Temimi, Marouane; Hareb, Fahad; Eibedingil, Iyasu

    2016-04-01

    In this study, an empirical algorithm was established to retrieve particulate matter (PM) concentrations (PM2.5 and PM10) using satellite-derived aerosol optical depth (AOD) over the United Arab Emirates (UAE). Validation of the proposed algorithm using ground truth data demonstrates its good accuracy. Time series of in situ measured PM concentrations between 2014 and 2015 showed high values in summer and low values in winter. Estimated and in situ measured PM concentrations were higher in 2015 than 2014. Remote sensing is an essential tool to reveal and back track the seasonality and inter-annual variations of PM concentrations and provide valuable information on the protection of human health and the response of air quality to anthropogenic activities and climate change.

  12. Chemical composition and mass closure of particulate matter at six urban sites in Europe

    NASA Astrophysics Data System (ADS)

    Sillanpää, Markus; Hillamo, Risto; Saarikoski, Sanna; Frey, Anna; Pennanen, Arto; Makkonen, Ulla; Spolnik, Zoya; Van Grieken, René; Braniš, Martin; Brunekreef, Bert; Chalbot, Marie-Cecile; Kuhlbusch, Thomas; Sunyer, Jordi; Kerminen, Veli-Matti; Kulmala, Markku; Salonen, Raimo O.

    The chemical composition of fine (PM 2.5) and coarse (PM 2.5-10) particulate matter was investigated in 7-week field campaigns of contrasting air pollution at six urban background sites in Europe. The campaigns were scheduled to include seasons of local public health concern due to high particulate concentrations or findings in previously conducted epidemiological studies. The sampling campaigns were carried out as follows: Duisburg/Germany October-November 2002 (autumn), Prague/Czech Republic November 2002-January 2003 (winter), Amsterdam/Netherlands January-March 2003 (winter), Helsinki/Finland March-May 2003 (spring), Barcelona/Spain March-May 2003 (spring) and Athens/Greece June-July 2003 (summer). Aerosol samples were collected in 3+4-day periods per week ( N=14) using two identical virtual impactors (VI). All the filter samples were analysed with the same instruments to obtain particulate mass, inorganic ions, total and watersoluble elements, and elemental and organic carbon content. The campaign means of PM 2.5 and PM 2.5-10 ranged from 8.3 to 30 and 5.4 to 29 μg m -3, respectively. The "wet and cool" seasons favoured a low coarse-to-fine particulate mass ratio (<1), whereas the ratio was high (>1) during the warmer and drier spring and summer campaigns. According to chemical mass closure, the major components in PM 2.5 were carbonaceous compounds (organic matter+elemental carbon), secondary inorganic ions and sea salt, whereas those in PM 2.5-10 were soil-derived compounds, carbonaceous compounds, sea salt and nitrate. The major and minor components together accounted for 79-106% and 77-96% of the gravimetrically measured PM 2.5 and PM 2.5-10 mass, respectively. In conclusion, the measured PM 2.5 and PM 2.5-10 in the campaigns could be reconstructed to a large extent with the help of harmonized particulate sampling and analysis of the selected chemical constituents. The health significance of the observed differences in chemical composition and emission

  13. Urban particulate matter pollution: a tale of five cities.

    PubMed

    Pandis, Spyros N; Skyllakou, Ksakousti; Florou, Kalliopi; Kostenidou, Evangelia; Kaltsonoudis, Christos; Hasa, Erion; Presto, Albert A

    2016-07-18

    Five case studies (Athens and Paris in Europe, Pittsburgh and Los Angeles in the United States, and Mexico City in Central America) are used to gain insights into the changing levels, sources, and role of atmospheric chemical processes in air quality in large urban areas as they develop technologically. Fine particulate matter is the focus of our analysis. In all cases reductions of emissions by industrial and transportation sources have resulted in significant improvements in air quality during the last few decades. However, these changes have resulted in the increasing importance of secondary particulate matter (PM) which dominates over primary in most cases. At the same time, long range transport of secondary PM from sources located hundreds of kilometres from the cities is becoming a bigger contributor to the urban PM levels in all seasons. "Non-traditional" sources including cooking, and residential and agricultural biomass burning contribute an increasing fraction of the now reduced fine PM levels. Atmospheric chemistry is found to change the chemical signatures of a number of these sources relatively fast both during the day and night, complicating the corresponding source apportionment.

  14. Organic and Elemental Carbon Aerosol Particulates at the Southern Great Plains Site Field Campaign Report

    SciTech Connect

    Cary, Robert

    2016-04-01

    The purpose of this study was to measure the organic carbon (OC) and elemental carbon (EC) fractions of PM2.5 particulate matter at the U.S. Department of Energy (DOE)’s Atmospheric Radiation Measurement (ARM) Climate Research Facility Southern Great Plains (SGP) sampling site for a 6-month period during the summer of 2013. The site is in a rural location remote from any populated areas, so it would be expected to reflect carbon concentration over long-distance transport patterns. During the same period in 2012, a number of prairie fires in Oklahoma and Texas had produced large plumes of smoke particles, but OC and EC particles had not been quantified. In addition, during the summer months, other wild fires, such as forest fires in the Rocky Mountain states and other areas, can produce carbon aerosols that are transported over long distances. Both of these source types would be expected to contain mixtures of both OC and EC.

  15. Particulate Matter Concentrations in East Oakland's High Street Corridor

    NASA Astrophysics Data System (ADS)

    Lei, P.; Jackson, J.; Lewis, R.; Marigny, A.; Mitchell, J. D.; Nguyen, R.; Philips, B.; Randle, D.; Romero, D.; Spears, D.; Telles, C.; Weissman, D.

    2012-12-01

    Particulate matter (PM) is a complex mixture of small solid pieces and/or liquid droplets in the air. High concentrations of PM can pose a serious health hazard because inhalation can result in breathing problems and/or aggravate asthma. Long term exposure can increase the likelihood of respiratory problems like asthma and emphysema as well as cancer. The smaller the particles, the deeper they can get into the respiratory system. For this reason, the smallest particles, those smaller than 2.5 micrometers in diameter (PM2.5), are the most dangerous. PM2.5 is largely emitted from motor vehicles burning fuels that don't break down fully. Our research team investigated the levels of PM2.5 as well as particles smaller than 10 micrometers (PM10) and total suspended particulate (TSP) along the northeast-southwest trending High Street Corridor, near Fremont High School in East Oakland, California. Using the Aerocet 531 mass particle counter, team members walked through neighborhoods and along major roads within a 1 mile radius of Fremont High School. The Aerocet 531 recorded two minute average measurements of all the relevant PM sizes, which are reported in mg/m3. Measurements were consistently taken in the morning, between 8:30 and 11:30 am. Preliminary results indicate maximum readings of all PM sizes at sites that are in close proximity to a major freeway (Interstate-880). These results support our initial hypothesis that proximity to major roads and freeways, especially those with high diesel-fuel burning truck traffic, would be the primary factor affecting PM concentration levels. Preliminary median and maximum readings all suggest particulate matter levels below what the EPA would consider unhealthy or risky.

  16. Effect of ozonation on particulate matter in broiler houses.

    PubMed

    Li, Q; Wang, L; Oviedo-Rondón, E; Parnell, C B

    2010-10-01

    The effects of ozonation on particulate matter were studied on a commercial broiler farm. The farm consisted of 4 identical tunnel-ventilated houses (12.8×152.4 m): 2 houses were treated with O3 (maximum concentration 0.1 ppm) and the other 2 served as control units. The particle size distributions of total suspended particulate (TSP) samples from both control and treated houses were found to have very similar profiles with no statistical difference. The TSP concentrations were significantly higher in treated houses as compared with those in control houses, and the mean of the differences was 5.50 mg/m3. In both treated and control houses, there were substantial vertical TSP concentration gradients and the concentrations decreased with height. At broiler chicken height (0.28 m), TSP concentrations were 13±3 mg/m3 in control houses and 17±2 mg/m3 in treated houses. At human breathing height (1.55 m), TSP concentrations were 8±4 mg/m3 in control houses and 7±2 mg/m3 in treated houses. Particle phase NH4+ concentrations were higher in treated houses (ranging from 0.59 to 42.01 mg/m3 with mean=17.49 mg/m3) than in control houses (ranging from 0.34 to 13.55 mg/m3 with mean=4.42 mg/m3). The TSP samples from locations in the vicinity of the farm showed higher concentrations downwind than that upwind, but there were no significant differences observed among different ambient locations for TSP NH4+ concentrations. The results from this study did not show that direct application of ozonation technique has beneficial effects for particulate matter control in broiler houses.

  17. Contribution of long range transport to local fine particulate matter concerns

    NASA Astrophysics Data System (ADS)

    Wagstrom, K. M.; Pandis, S. N.

    2011-05-01

    We have utilized the Particulate Matter Source Apportionment Technology (PSAT) in PMCAMx (a regional chemical transport model) to quantify the contributions from local emissions and short range (under 100 km), mid range (100-550 km) and long range (over 550 km) pollutant transport to both primary and secondary particulate matter concentrations using the Eastern United States as a test case. We have studied these contributions for two urban (Pittsburgh, Pennsylvania and Atlanta, Georgia) and one rural area (Great Smoky Mountains National Park) during all seasons. The local emissions impacts to elemental carbon (EC) in major urban areas were found to be substantial with approximately 50% of the EC coming from local sources and 80% emitted within 200 km of the receptor. The local sources are even more important during the night contributing around 60% of the EC and then dropping to around 40% during the early afternoon. The EC in the rural Great Smoky Mountains was mainly the result of sources 100-550 km away. The seasonal variation of the EC source area contributions is small. There was also little difference between high and low EC concentration days. The contributions to secondary aerosol species were found to be more regional with more than 50% of the sulfate and secondary organic aerosol (SOA) originating from SO 2 and VOC sources that were more than 200 km away from the receptor. The importance of sources further away increased during the winter because of the lower photochemical activity. While mid range transport dominated in the summer the sulfate and SOA levels in all areas, long range transport became the most important sulfate and SOA source during the winter in the colder Northeastern US and of sulfate in the warmer South.

  18. Adverse effect of diesel engine produced particulate matter on various stone types and concrete: a laboratory exposure experiment

    NASA Astrophysics Data System (ADS)

    Farkas, Orsolya; Szabados, György; Antal, Ákos; Török, Ákos

    2015-04-01

    The effect of particulate matter on construction materials have been studied under laboratory conditions. For testing the adverse effects of diesel soot and particulate matter on stone and concrete a small scale laboratory exposure chamber was constructed. Blocks of 9 different stone types and concrete was placed in the chamber and an exhaust pipe of diesel engine was diverted into the system. Tested stones included: porous limestone, cemented non-porous limestone, travertine, marble, rhyolite tuff, andesite and granite. The engine was operated for 10 hours and the produced particulate matter was diverted directly to the surface of the material specimens of 3 cm in diameter each. Working parameters of the engine were controlled; the composition of the exhaust gas, smoke value and temperature were continuously measured during the test. Test specimens were documented and analysed prior to exposure and after the exposure test. Parameters such colorimetric values, weight, surface properties, mineralogical compositions of the test specimens were recorded. The working temperature was in the order of 300°C-320°C. The gas concentration was in ppm as follows: 157 CO; 5.98 CO2, 34.3 THC; 463 NOx; 408 NO; 12.88 O2. Our tests have demonstrated that significant amount of particulate matter was deposited on construction materials even at a short period of time; however the exposure was very intense. It also indicates that that the interaction of particulate matter and aerosol compounds with construction materials in urban areas causes rapid decay and has an adverse effect not only on human health but also on built structures.

  19. Compositional Analysis of Fine Particulate Matter in Fairbanks, Alaska

    NASA Astrophysics Data System (ADS)

    Nattinger, K.; Simpson, W. R.; Huff, D.

    2015-12-01

    Fairbanks, AK experiences extreme pollution episodes that result in winter violations of the fine particulate matter (PM2.5) National Ambient Air Quality Standards. This poses a significant health risk for the inhabitants of the area. These high levels result from trapping of pollution in a very shallow boundary layer due to local meteorology, but the role of primary (direct emission) of particulate matter versus secondary production (in the atmosphere) of particulate matter is not understood. Analysis of the PM2.5 composition is being conducted to provide insight into sources, trends, and chemistry. Methods are developed to convert carbon data from IMPROVE (post-2009 analysis method) to NIOSH (pre-2009 method) utilizing blank subtraction, sampler bias adjustment, and inter-method correlations from co-located samples. By converting all carbon measurements to a consistent basis, long-term trends can be analyzed. The approach shows excellent mass closure between PM2.5 mass reconstructed from constituents and gravimetric-analyzed mass. This approach could be utilized in other US locations where the carbon analysis methods also changed. Results include organic and inorganic fractional mass percentages, analyzed over an eight-year period for two testing sites in Fairbanks and two in the nearby city of North Pole. We focus on the wintertime (Nov—Feb) period when most air quality violations occur and find that the particles consist primarily of organic carbon, with smaller percentages of sulfate, elemental carbon, ammonium, and nitrate. The Fairbanks area PM2.5 organic carbon / elemental carbon partitioning matches the source profile of wood smoke. North Pole and Fairbanks PM2.5 have significant compositional differences, with North Pole having a larger percentage of organic matter. Mass loadings in SO42-, NO3-, and total PM2.5 mass correlate with temperature. Multi-year temporal trends show little if any change with a strong effect from temperature. Insights from this

  20. 75 FR 65567 - Approval and Promulgation of Air Quality Implementation Plans; Ohio; Particulate Matter Standards

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-10-26

    ... AGENCY 40 CFR Part 52 Approval and Promulgation of Air Quality Implementation Plans; Ohio; Particulate... requirements. The particulate matter (PM) standards contain the particulate emission control requirements that have been necessary to attain and maintain the 2006 National Ambient Air Quality Standards (NAAQS)...

  1. Source apportionment of fine and coarse particulate matter in a sub-urban area at the Western European Coast

    NASA Astrophysics Data System (ADS)

    Almeida, S. M.; Pio, C. A.; Freitas, M. C.; Reis, M. A.; Trancoso, M. A.

    Aerosol chemical composition data for PM 2.5 and PM 10-2.5, was acquired during the year 2001 at a sub-urban area located in the north outskirts of Lisbon. Principal component analysis (PCA) and multilinear regression analysis (MLRA) were used to identify possible sources of particulate matter (PM) and to determine their mass contribution. Seven main groups of sources were identified: soil, sea, secondary aerosols, road traffic, fuel-oil combustion, coal combustion and a Se/Hg emission source. In PM 2.5, secondary aerosol and vehicle exhaust contributed on average, with 25% and 22% to total mass, respectively, while sea spray and soil represented, respectively, 47% and 20% of the coarse fraction mass loading. Maritime air mass transport has a significant role on air quality in the North of Lisbon. Maritime transport scenarios are very frequent and promote the decrease of anthropogenic and mineral aerosol concentrations. The highest PM levels were recorded during South Continental episodes. These episodes are characterized by high mineral aerosol contents, due to the transport of dust from the interior of Iberian Peninsula and the Sahara desert. After identifying the contribution of PM sources, it is possible to conclude that abatement strategies to improve local air quality should focus on traffic and on non-mobile combustion processes emitting sulphur and NO x, which conduce to the formation of secondary aerosols.

  2. Qualitative and quantitative determination of water in airborne particulate matter

    NASA Astrophysics Data System (ADS)

    Canepari, S.; Farao, C.; Marconi, E.; Giovannelli, C.; Perrino, C.

    2012-10-01

    This paper describes the optimization and validation of a new simple method for the quantitative determination of water in atmospheric particulate matter (PM). The analyses are performed by using a coulometric Karl-Fisher system equipped with a controlled heating device; different water contributions are separated by the application of an optimized thermal ramp (three heating steps: 50-120 °C, 120-180 °C, 180-250 °C). The analytical performance of the method was verified by using standard materials containing 5.55% and 1% by weight of water. The recovery was greater than 95%; the detection limit was about 20 μg. The method was then applied to NIST reference materials (NIST1649a, urban particulate matter) and to real PM10 samples collected in different geographical areas. In all cases the repeatability was satisfactory (10-15%). When analyzing the reference material, the separation of four different types of water was obtained. In real PM10 samples the amount of water and its thermal profile differed as a function of the chemical composition of the dust. Mass percentages of 3-4% of water were obtained in most samples, but values up to about 15% were reached in areas where the chemical composition of PM is dominated by secondary inorganic ions and organic matter. High percentages of water were also observed in areas where PM is characterized by the presence of desert dust. A possible identification of the quality of water released from the samples was tried by applying the method to some hygroscopic compounds that are likely contained in PM (pure SiO2, Al2O3, ammonium salts, carbohydrates and dicarboxylic acids) and by comparing the results with those obtained from field samples.

  3. Qualitative and quantitative determination of water in airborne particulate matter

    NASA Astrophysics Data System (ADS)

    Canepari, S.; Farao, C.; Marconi, E.; Giovannelli, C.; Perrino, C.

    2013-02-01

    This paper describes the optimization and validation of a new simple method for the quantitative determination of water in atmospheric particulate matter (PM). The analyses are performed by using a coulometric Karl-Fisher system equipped with a controlled heating device; different water contributions are separated by the application of an optimized thermal ramp (three heating steps: 50-120 °C, 120-180 °C, 180-250 °C). The analytical performance of the method was verified by using standard materials containing 5.55% and 1% by weight of water. The recovery was greater than 95%; the detection limit was about 20 μg. The method was then applied to NIST Reference Materials (NIST1649a, urban particulate matter) and to real PM10 samples collected in different geographical areas. In all cases the repeatability was satisfactory (10-15%). When analyzing the Reference Material, the separation of four different types of water was obtained. In real PM10 samples the amount of water and its thermal profile differed as a function of the chemical composition of the dust. Mass percentages of 3-4% of water were obtained in most samples, but values up to about 15% were reached in areas where the chemical composition of PM is dominated by secondary inorganic ions and organic matter. High percentages of water were also observed in areas where PM is characterized by the presence of desert dust. A possible identification of the quality of water released from the samples was tried by applying the method to some hygroscopic compounds that are likely contained in PM (pure SiO2, Al2O3, ammonium salts, carbohydrates and dicarboxylic acids) and by comparing the results with those obtained from field samples.

  4. 77 FR 12769 - Approval and Promulgation of Implementation Plans; Georgia; Macon; Fine Particulate Matter 2002...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-02

    ... Matter 2002 Base Year Emissions Inventory AGENCY: Environmental Protection Agency (EPA). ACTION: Proposed rule. SUMMARY: EPA is proposing to approve the fine particulate matter (PM 2.5 ) 2002 base...

  5. Development of emission factors for particulate matter in a school

    SciTech Connect

    Scheff, P.A.; Paulius, V.; Conroy, L.M.

    1999-07-01

    Schools have complex indoor environments which are influenced by many factors such as number of occupants, building design, office equipment, cleaning agents, and school activities. Like large office buildings, school environments may be adversely influenced by deficiencies in ventilation which may be due to improper operation of HVAC systems, attempts at energy efficiency that limit the supply of outdoor air, or remodeling of building components. Most importantly, children spend up to a third of their time in these structures, and thus it is desirable to better understand the environmental quality in these buildings. A middle school (grades 6 to 8) in a residential section of Springfield, IL was selected for this baseline indoor air quality survey. The school was characterized as having no health complaints, good maintenance schedules, and did not contain carpeting within the classrooms or hallways. The focus of this paper is on the measurements of air quality in the school. The development of emission factors for particulate matter is also discussed. Four indoor locations including the Cafeteria, a Science Classroom, an Art Classroom, and the Lobby outside of the main office, and one outdoor location were sampled for various environmental comfort and pollutant parameters for one week in February of 1997. Integrated samples (8 hour sampling time) for respirable and total particulate matter, and short-term measurements of bioaerosols (two minute samples, three times per day) on three consecutive days were collected at each of the indoor and outdoor sites. Continuous measurements of carbon dioxide, carbon monoxide, temperature and humidity were logged at all locations for five days. Continuous measurements of respirable particulate matter were also collected in the Lobby area. Detailed logs of occupant activity were also collected at each indoor monitoring location throughout the study. Total particle concentrations ranged from 29 to 177 {micro}g/m{sup 3} in the art

  6. Urban-scale variability of ambient particulate matter attributes

    NASA Astrophysics Data System (ADS)

    Freiman, M. T.; Hirshel, N.; Broday, D. M.

    Real-time sampling of ambient particulate matter (PM) in the size range 0.23-10 μm and of carbonaceous matter concentrations has been carried out in a carefully designed field campaign in proximate paired neighborhoods in Haifa, Israel. The paired sites are characterized by a similar population density and neighborhood-wise socioeconomic (deprivation) index but show distinct canopy coverage. The data indicate clear sub-urban (neighborhood) scale variations in any measured PM attribute, such as concentrations, size distribution, and carbonaceous matter content. Mean ambient PM levels were comparatively higher than in other urban studies whereas carbonaceous airborne PM concentrations were lower. On top of the diurnal and seasonal variability and in spite of the significant regional effect of the semi-arid climate, local emissions and removal processes affect the PM concentrations to which people residing in urbanized regions are exposed. Analysis of possible mechanisms that could affect the observed spatial sub-urban PM differences, including local meteorology and emissions, reveal that sub-urban variability of removal processes has a major influence on ambient PM levels. Observations suggest that on top of the regional air masses which affect the city air quality and emissions from local sources, a normally unnoticed removal process, showing urban scale variability, is interception by trees and dense vegetation. In particular, the observed sub-urban variability in ambient PM concentrations is attributed, in part, to local variation of removal processes, among them the neighborhood-wise deposition on available surfaces, including canopy.

  7. 77 FR 38760 - National Ambient Air Quality Standards for Particulate Matter; Correction

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-06-29

    ... AGENCY 40 CFR Parts 50, 51, 52, 53, and 58 RIN 2060-AO47 National Ambient Air Quality Standards for... revise the national ambient air quality standards (NAAQS) for particulate matter (PM). This action...: Questions concerning the ``National Ambient Air Quality Standards for Particulate Matter'' proposed...

  8. 78 FR 3085 - National Ambient Air Quality Standards for Particulate Matter

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-01-15

    ... Air Quality Standards for Particulate Matter; Final Rule #0;#0;Federal Register / Vol. 78 , No. 10..., 51, 52, 53 and 58 RIN 2060-AO47 National Ambient Air Quality Standards for Particulate Matter AGENCY: Environmental Protection Agency (EPA). ACTION: Final rule. SUMMARY: Based on its review of the air...

  9. 40 CFR 49.126 - Rule for limiting fugitive particulate matter emissions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... AND OTHER FEDERAL ASSISTANCE TRIBAL CLEAN AIR ACT AUTHORITY General Federal Implementation Plan... amount of fugitive particulate matter that may be emitted from certain air pollution sources operating... dwelling units. (d) What are the requirements for sources of fugitive particulate matter emissions? (1)...

  10. Evaluating the effectiveness of vegetative environmental buffers in mitigating particulate matter emissions from poultry houses

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Particulate Matter (PM) emissions from animal operations have been identified as a major air pollutant source with health and environmental impacts. Nearly 600 million broilers are produced annually on the Delmarva Peninsula, making it a hot spot for particulate matter emissions from poultry houses....

  11. SUMMARY FINDINGS FROM THE U.S. EPA'S PARTICULATE MATTER PANEL STUDIES

    EPA Science Inventory

    The U.S. EPA's Particulate Matter Panel Studies were a series of longitudinal human exposure studies used to characterize personal exposures to particulate matter (PM) and related co-pollutants to that of pollutants of ambient origin. Participants were monitored over time (28 d...

  12. 40 CFR 52.228 - Regulations: Particulate matter, Southeast Desert Intrastate Region.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ..., Southeast Desert Intrastate Region. 52.228 Section 52.228 Protection of Environment ENVIRONMENTAL PROTECTION... § 52.228 Regulations: Particulate matter, Southeast Desert Intrastate Region. (a) The following... particulate matter in the Southeast Desert Intrastate Region. (1) Imperial County Air Pollution...

  13. 40 CFR 52.228 - Regulations: Particulate matter, Southeast Desert Intrastate Region.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ..., Southeast Desert Intrastate Region. 52.228 Section 52.228 Protection of Environment ENVIRONMENTAL PROTECTION... § 52.228 Regulations: Particulate matter, Southeast Desert Intrastate Region. (a) The following... particulate matter in the Southeast Desert Intrastate Region. (1) Imperial County Air Pollution...

  14. 40 CFR 52.228 - Regulations: Particulate matter, Southeast Desert Intrastate Region.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ..., Southeast Desert Intrastate Region. 52.228 Section 52.228 Protection of Environment ENVIRONMENTAL PROTECTION... § 52.228 Regulations: Particulate matter, Southeast Desert Intrastate Region. (a) The following... particulate matter in the Southeast Desert Intrastate Region. (1) Imperial County Air Pollution...

  15. 40 CFR 52.228 - Regulations: Particulate matter, Southeast Desert Intrastate Region.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ..., Southeast Desert Intrastate Region. 52.228 Section 52.228 Protection of Environment ENVIRONMENTAL PROTECTION... § 52.228 Regulations: Particulate matter, Southeast Desert Intrastate Region. (a) The following... particulate matter in the Southeast Desert Intrastate Region. (1) Imperial County Air Pollution...

  16. 40 CFR 52.228 - Regulations: Particulate matter, Southeast Desert Intrastate Region.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ..., Southeast Desert Intrastate Region. 52.228 Section 52.228 Protection of Environment ENVIRONMENTAL PROTECTION... § 52.228 Regulations: Particulate matter, Southeast Desert Intrastate Region. (a) The following... particulate matter in the Southeast Desert Intrastate Region. (1) Imperial County Air Pollution...

  17. 40 CFR 52.2306 - Particulate Matter (PM10) Group II SIP commitments.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 5 2014-07-01 2014-07-01 false Particulate Matter (PM10) Group II SIP... Particulate Matter (PM10) Group II SIP commitments. On July 18, 1988, the Governor of Texas submitted a revision to the State Implementation Plan (SIP) that contained commitments for implementing all of...

  18. 40 CFR 52.2306 - Particulate Matter (PM10) Group II SIP commitments.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Particulate Matter (PM10) Group II SIP... Particulate Matter (PM10) Group II SIP commitments. On July 18, 1988, the Governor of Texas submitted a revision to the State Implementation Plan (SIP) that contained commitments for implementing all of...

  19. 40 CFR 52.1489 - Particulate matter (PM-10) Group II SIP commitments.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 4 2014-07-01 2014-07-01 false Particulate matter (PM-10) Group II SIP... Particulate matter (PM-10) Group II SIP commitments. (a) On March 29, 1989, the Air Quality Officer for the... inventory, and other tasks that may be necessary to satisfy the requirements of the PM-10 Group II SIPs....

  20. 40 CFR 52.1489 - Particulate matter (PM-10) Group II SIP commitments.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Particulate matter (PM-10) Group II SIP... Particulate matter (PM-10) Group II SIP commitments. (a) On March 29, 1989, the Air Quality Officer for the... inventory, and other tasks that may be necessary to satisfy the requirements of the PM-10 Group II SIPs....

  1. 40 CFR 52.1637 - Particulate Matter (PM10) Group II SIP commitments.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Particulate Matter (PM10) Group II SIP... Particulate Matter (PM10) Group II SIP commitments. (a) On August 19, 1988, the Governor of New Mexico submitted a revision to the State Implementation Plan (SIP) that contained commitments, from the Director...

  2. 40 CFR 52.1637 - Particulate Matter (PM10) Group II SIP commitments.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Particulate Matter (PM10) Group II SIP... Particulate Matter (PM10) Group II SIP commitments. (a) On August 19, 1988, the Governor of New Mexico submitted a revision to the State Implementation Plan (SIP) that contained commitments, from the Director...

  3. 40 CFR 52.1489 - Particulate matter (PM-10) Group II SIP commitments.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Particulate matter (PM-10) Group II SIP... Particulate matter (PM-10) Group II SIP commitments. (a) On March 29, 1989, the Air Quality Officer for the... inventory, and other tasks that may be necessary to satisfy the requirements of the PM-10 Group II SIPs....

  4. 40 CFR 52.2306 - Particulate Matter (PM10) Group II SIP commitments.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Particulate Matter (PM10) Group II SIP... Particulate Matter (PM10) Group II SIP commitments. On July 18, 1988, the Governor of Texas submitted a revision to the State Implementation Plan (SIP) that contained commitments for implementing all of...

  5. 40 CFR 52.2306 - Particulate Matter (PM10) Group II SIP commitments.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 5 2013-07-01 2013-07-01 false Particulate Matter (PM10) Group II SIP... Particulate Matter (PM10) Group II SIP commitments. On July 18, 1988, the Governor of Texas submitted a revision to the State Implementation Plan (SIP) that contained commitments for implementing all of...

  6. 40 CFR 52.1489 - Particulate matter (PM-10) Group II SIP commitments.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Particulate matter (PM-10) Group II SIP... Particulate matter (PM-10) Group II SIP commitments. (a) On March 29, 1989, the Air Quality Officer for the... inventory, and other tasks that may be necessary to satisfy the requirements of the PM-10 Group II SIPs....

  7. 40 CFR 52.2306 - Particulate Matter (PM10) Group II SIP commitments.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 5 2012-07-01 2012-07-01 false Particulate Matter (PM10) Group II SIP... Particulate Matter (PM10) Group II SIP commitments. On July 18, 1988, the Governor of Texas submitted a revision to the State Implementation Plan (SIP) that contained commitments for implementing all of...

  8. 40 CFR 52.1637 - Particulate Matter (PM10) Group II SIP commitments.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Particulate Matter (PM10) Group II SIP... Particulate Matter (PM10) Group II SIP commitments. (a) On August 19, 1988, the Governor of New Mexico submitted a revision to the State Implementation Plan (SIP) that contained commitments, from the Director...

  9. 40 CFR 52.1637 - Particulate Matter (PM10) Group II SIP commitments.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Particulate Matter (PM10) Group II SIP... Particulate Matter (PM10) Group II SIP commitments. (a) On August 19, 1988, the Governor of New Mexico submitted a revision to the State Implementation Plan (SIP) that contained commitments, from the Director...

  10. 40 CFR 52.1489 - Particulate matter (PM-10) Group II SIP commitments.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Particulate matter (PM-10) Group II SIP... Particulate matter (PM-10) Group II SIP commitments. (a) On March 29, 1989, the Air Quality Officer for the... inventory, and other tasks that may be necessary to satisfy the requirements of the PM-10 Group II SIPs....

  11. 40 CFR 52.1637 - Particulate Matter (PM10) Group II SIP commitments.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 4 2014-07-01 2014-07-01 false Particulate Matter (PM10) Group II SIP... Particulate Matter (PM10) Group II SIP commitments. (a) On August 19, 1988, the Governor of New Mexico submitted a revision to the State Implementation Plan (SIP) that contained commitments, from the Director...

  12. GENETIC INFLUENCES ON IN VTIRO PARTICULATE MATTER-INDUCED AIRWAY EPITHELIAL INJURY AND INFLAMMATORY MEDIATOR RELEASE

    EPA Science Inventory

    GENETIC INFLUENCES ON IN VITRO PARTICULATE MATTER-INDUCED AIRWAY EPITHELIAL INJURY AND INFLAMMATORY MEDIATOR RELEASE.
    JA Dye, JH Richards, DA Andrews, UP Kodavanti. US EPA, RTP, NC, USA.

    Particulate matter (PM) air pollution is capable of damaging the airway epitheli...

  13. Ambient particulate matter accelerates coagulation via an IL-6-dependent pathway

    EPA Science Inventory

    The mechanisms by which exposure to particulate matter increases the risk of cardiovascular events are not known. Recent human and animal data suggest that particulate matter may induce alterations in hemostatic factors. In this study we determined the mechanisms by which particu...

  14. 40 CFR 52.528 - Control strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 3 2014-07-01 2014-07-01 false Control strategy: Sulfur oxides and particulate matter. 52.528 Section 52.528 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... strategy: Sulfur oxides and particulate matter. (a) In a letter dated October 10, 1986, the...

  15. 40 CFR 52.528 - Control strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 3 2013-07-01 2013-07-01 false Control strategy: Sulfur oxides and particulate matter. 52.528 Section 52.528 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... strategy: Sulfur oxides and particulate matter. (a) In a letter dated October 10, 1986, the...

  16. A Literature Review of Concentrations and Size Distributions of Ambient Airborne Pb-Containing Particulate Matter

    EPA Science Inventory

    The final 2008 lead (Pb) national ambient air quality standards (NAAQS) revision maintains Pb in total suspended particulate matter as the indicator. However, the final rule permits the use of low-volume PM10 (particulate matter sampled with a 50% cut-point of 10 μm) F...

  17. 40 CFR 52.2231 - Control strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 5 2012-07-01 2012-07-01 false Control strategy: Sulfur oxides and particulate matter. 52.2231 Section 52.2231 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... § 52.2231 Control strategy: Sulfur oxides and particulate matter. (a) Part D conditional approval....

  18. 40 CFR 52.2231 - Control strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Sulfur oxides and particulate matter. 52.2231 Section 52.2231 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... § 52.2231 Control strategy: Sulfur oxides and particulate matter. (a) Part D conditional approval....

  19. 40 CFR 52.578 - Control Strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 3 2014-07-01 2014-07-01 false Control Strategy: Sulfur oxides and particulate matter. 52.578 Section 52.578 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Strategy: Sulfur oxides and particulate matter. In a letter dated March 26, 1987, the Georgia Department...

  20. 40 CFR 52.2130 - Control strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Sulfur oxides and particulate matter. 52.2130 Section 52.2130 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Carolina § 52.2130 Control strategy: Sulfur oxides and particulate matter. In letters dated May 7,...

  1. 40 CFR 52.2231 - Control strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 5 2014-07-01 2014-07-01 false Control strategy: Sulfur oxides and particulate matter. 52.2231 Section 52.2231 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... § 52.2231 Control strategy: Sulfur oxides and particulate matter. (a) Part D conditional approval....

  2. 40 CFR 52.2231 - Control strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Sulfur oxides and particulate matter. 52.2231 Section 52.2231 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... § 52.2231 Control strategy: Sulfur oxides and particulate matter. (a) Part D conditional approval....

  3. 40 CFR 52.578 - Control Strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 3 2013-07-01 2013-07-01 false Control Strategy: Sulfur oxides and particulate matter. 52.578 Section 52.578 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Strategy: Sulfur oxides and particulate matter. In a letter dated March 26, 1987, the Georgia Department...

  4. 40 CFR 52.578 - Control Strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 3 2012-07-01 2012-07-01 false Control Strategy: Sulfur oxides and particulate matter. 52.578 Section 52.578 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Strategy: Sulfur oxides and particulate matter. In a letter dated March 26, 1987, the Georgia Department...

  5. 40 CFR 52.1781 - Control strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Sulfur oxides and particulate matter. 52.1781 Section 52.1781 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Carolina § 52.1781 Control strategy: Sulfur oxides and particulate matter. (a) The plan's control...

  6. 40 CFR 52.2231 - Control strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 5 2013-07-01 2013-07-01 false Control strategy: Sulfur oxides and particulate matter. 52.2231 Section 52.2231 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... § 52.2231 Control strategy: Sulfur oxides and particulate matter. (a) Part D conditional approval....

  7. 40 CFR 52.2130 - Control strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Sulfur oxides and particulate matter. 52.2130 Section 52.2130 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Carolina § 52.2130 Control strategy: Sulfur oxides and particulate matter. In letters dated May 7,...

  8. 40 CFR 52.2130 - Control strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 5 2012-07-01 2012-07-01 false Control strategy: Sulfur oxides and particulate matter. 52.2130 Section 52.2130 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Carolina § 52.2130 Control strategy: Sulfur oxides and particulate matter. In letters dated May 7,...

  9. 40 CFR 52.933 - Control Strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 3 2010-07-01 2010-07-01 false Control Strategy: Sulfur oxides and particulate matter. 52.933 Section 52.933 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Strategy: Sulfur oxides and particulate matter. In a letter dated March 27, 1987, the Kentucky...

  10. 40 CFR 52.1781 - Control strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Sulfur oxides and particulate matter. 52.1781 Section 52.1781 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Carolina § 52.1781 Control strategy: Sulfur oxides and particulate matter. (a) The plan's control...

  11. 40 CFR 52.578 - Control Strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 3 2010-07-01 2010-07-01 false Control Strategy: Sulfur oxides and particulate matter. 52.578 Section 52.578 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Strategy: Sulfur oxides and particulate matter. In a letter dated March 26, 1987, the Georgia Department...

  12. 40 CFR 52.933 - Control Strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 3 2011-07-01 2011-07-01 false Control Strategy: Sulfur oxides and particulate matter. 52.933 Section 52.933 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Strategy: Sulfur oxides and particulate matter. (a) In a letter dated March 27, 1987, the...

  13. 40 CFR 52.62 - Control strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 3 2010-07-01 2010-07-01 false Control strategy: Sulfur oxides and particulate matter. 52.62 Section 52.62 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... strategy: Sulfur oxides and particulate matter. In a letter dated May 29, 1987, the Alabama Department...

  14. 40 CFR 52.2130 - Control strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 5 2013-07-01 2013-07-01 false Control strategy: Sulfur oxides and particulate matter. 52.2130 Section 52.2130 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Carolina § 52.2130 Control strategy: Sulfur oxides and particulate matter. In letters dated May 7,...

  15. 40 CFR 52.2130 - Control strategy: Sulfur oxides and particulate matter.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 5 2014-07-01 2014-07-01 false Control strategy: Sulfur oxides and particulate matter. 52.2130 Section 52.2130 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Carolina § 52.2130 Control strategy: Sulfur oxides and particulate matter. In letters dated May 7,...

  16. Plant species differences in particulate matter accumulation on leaf surfaces.

    PubMed

    Sæbø, A; Popek, R; Nawrot, B; Hanslin, H M; Gawronska, H; Gawronski, S W

    2012-06-15

    Particulate matter (PM) accumulation on leaves of 22 trees and 25 shrubs was examined in test fields in Norway and Poland. Leaf PM in different particle size fractions (PM(10), PM(2.5), PM(0.2)) differed among the species, by 10- to 15-folds at both test sites. Pinus mugo and Pinus sylvestris, Taxus media and Taxus baccata, Stephanandra incisa and Betula pendula were efficient species in capturing PM. Less efficient species were Acer platanoides, Prunus avium and Tilia cordata. Differences among species within the same genus were also observed. Important traits for PM accumulation were leaf properties such as hair and wax cover. The ranking presented in terms of capturing PM can be used to select species for air pollution removal in urban areas. Efficient plant species and planting designs that can shield vulnerable areas in urban settings from polluting traffic etc. can be used to decrease human exposure to anthropogenic pollutants.

  17. High exhaust temperature, zoned, electrically-heated particulate matter filter

    DOEpatents

    Gonze, Eugene V.; Paratore, Jr., Michael J.; Bhatia, Garima

    2015-09-22

    A system includes a particulate matter (PM) filter, an electric heater, and a control circuit. The electric heater includes multiple zones, which each correspond to longitudinal zones along a length of the PM filter. A first zone includes multiple discontinuous sub-zones. The control circuit determines whether regeneration is needed based on an estimated level of loading of the PM filter and an exhaust flow rate. In response to a determination that regeneration is needed, the control circuit: controls an operating parameter of an engine to increase an exhaust temperature to a first temperature during a first period; after the first period, activates the first zone; deactivates the first zone in response to a minimum filter face temperature being reached; subsequent to deactivating the first zone, activates a second zone; and deactivates the second zone in response to the minimum filter face temperature being reached.

  18. Fine particulate matter in acute exacerbation of COPD

    PubMed Central

    Ni, Lei; Chuang, Chia-Chen; Zuo, Li

    2015-01-01

    Chronic obstructive pulmonary disease (COPD) is a common airway disorder. In particular, acute exacerbations of COPD (AECOPD) can significantly reduce pulmonary function. The majority of AECOPD episodes are attributed to infections, although environmental stress also plays a role. Increasing urbanization and associated air pollution, especially in developing countries, have been shown to contribute to COPD pathogenesis. Elevated levels of particulate matter (PM) in polluted air are strongly correlated with the onset and development of various respiratory diseases. In this review, we have conducted an extensive literature search of recent studies of the role of PM2.5 (fine PM) in AECOPD. PM2.5 leads to AECOPD via inflammation, oxidative stress (OS), immune dysfunction, and altered airway epithelial structure and microbiome. Reducing PM2.5 levels is a viable approach to lower AECOPD incidence, attenuate COPD progression and decrease the associated healthcare burden. PMID:26557095

  19. Deposition of heavy metals from particulate settleable matter in soils of an industrialized area

    NASA Astrophysics Data System (ADS)

    Sanfeliu, Teófilo

    2010-05-01

    Particulate air pollutants from industrial emissions and natural resource exploitation represent an important contribution to soil contamination. These atmospheric particles, usually settleable particulate matter form (which settle by gravity) are deposited on soil through both dry and wet. The most direct consequences on soil of air pollutants are acidification and salinization, not to mention the pollution that can cause heavy metals as components of suspended particulate matter. The main objective of this study was to evaluate the influence of air pollution in soil composition. For this purpose, has been conducted a study of the composition of heavy metals in the settleable particulate matter in two locations (Almazora and Vila-real) with high industrial density (mainly ceramic companies) located in the ceramic cluster of Castellón (Spain). Settleable air particles samples were collected with a PS Standard Britannic captor (MCV-PS2) for monthly periods between January 2007 and December 2009. We analyzed the following elements: Cd, Pb, Cu, Ni, Sb and Bi which are highly toxic and have the property of accumulating in living organisms. It has been determined the concentration of heavy metals in the soluble fraction of settleable air particles by ICP-MS. The annual variation of the results obtained in both populations shows a decline over the study period the concentrations of heavy metals analyzed. This fact is associated with the steady implementation of corrective measures in the main industrial sector in the area based on the treatment of mineral raw materials. Moreover, this decline is, in turn, a lower intake of heavy metals to the soil. REFERENCES Gómez E.T.; Sanfeliu T.; Rius J.; Jordán M.M. (2005) "Evolution, sources and distribution of mineral particles and amorphous phase of atmospheric aerosol in an industrial and Mediterranean coastal area" Water, air and Soil Pollution 167:311-330 Moral R., Gilkes R.J.; Jordán M.M. (2005) "Distribution of heavy

  20. The Stable and Radio- Carbon Isotopic Content of Labile and Refractory Carbon in Atmospheric Particulate Matter

    NASA Astrophysics Data System (ADS)

    McNichol, A. P.; Rosenheim, B. E.; Gerlach, D. S.; Hayes, J. M.

    2006-12-01

    Studies of the isotopic content of atmospheric particulate matter are hampered by difficulties in chemically defining the pools of carbon and analytically isolating the different pools. We are conducting studies on reference materials and atmospheric aerosol samples to develop a method to measure stable and radio- carbon isotopes on the labile and refractory carbon. We are using a flow-through combustion system that allows us to combust, collect and measure the isotopic content of the gases produced at all stages of heating/oxidizing. We compare our results to those measured using a chemothermal oxidation method (CTO) (Gustafsson et al., 2001). In this method, refractory carbon is defined as the material remaining after pre- combusting a sample at 375°C in the presence of oxygen for 24 hours. The reference materials are diesel soot, apple leaves and a hybrid of the two (DiesApple), all from NIST. These provide carbon with two well-defined fractions -- the soot provides refractory carbon that is radiocarbon dead and the apple leaves provide organic carbon that is radiocarbon modern. Radiocarbon results from DiesApple indicate that the "refractory" carbon defined by the CTO method is actually a mixture of old and modern carbon that contains over 25% modern carbon. This suggests that charred material formed from the apples leaves during the pre-combustion step is contributing to the fraction we identify as refractory carbon. We are studying this by analyzing the individual materials and the mixture using our flow-through system. First results with this system indicate that the refractory fraction trapped from the DiesApple contains much less modern carbon than the CTO method, less than 7%. We will present detailed concentration and isotopic results of the generation of carbon dioxide during programmed combustion of each of the reference materials. We studied the radiocarbon content of both the total carbon (TC) and refractory carbon in the fine particulate matter (PM

  1. Gaseous pollutants in particulate matter epidemiology: confounders or surrogates?

    PubMed Central

    Sarnat, J A; Schwartz, J; Catalano, P J; Suh, H H

    2001-01-01

    Air pollution epidemiologic studies use ambient pollutant concentrations as surrogates of personal exposure. Strong correlations among numerous ambient pollutant concentrations, however, have made it difficult to determine the relative contribution of each pollutant to a given health outcome and have led to criticism that health effect estimates for particulate matter may be biased due to confounding. In the current study we used data collected from a multipollutant exposure study conducted in Baltimore, Maryland, during both the summer and winter to address the potential for confounding further. Twenty-four-hour personal exposures and corresponding ambient concentrations to fine particulate matter (PM(2.5)), ozone, nitrogen dioxide, sulfur dioxide, and carbon monoxide were measured for 56 subjects. Results from correlation and regression analyses showed that personal PM(2.5) and gaseous air pollutant exposures were generally not correlated, as only 9 of the 178 individual-specific pairwise correlations were significant. Similarly, ambient concentrations were not associated with their corresponding personal exposures for any of the pollutants, except for PM(2.5), which had significant associations during both seasons (p < 0.0001). Ambient gaseous concentrations were, however, strongly associated with personal PM(2.5) exposures. The strongest associations were shown between ambient O(3) and personal PM(2.5) (p < 0.0001 during both seasons). These results indicate that ambient PM(2.5) concentrations are suitable surrogates for personal PM(2.5) exposures and that ambient gaseous concentrations are surrogates, as opposed to confounders, of PM(2.5). These findings suggest that the use of multiple pollutant models in epidemiologic studies of PM(2.5) may not be suitable and that health effects attributed to the ambient gases may actually be a result of exposures to PM(2.5). PMID:11675271

  2. Acute pulmonary toxicity of urban particulate matter and ozone.

    PubMed Central

    Vincent, R.; Bjarnason, S. G.; Adamson, I. Y.; Hedgecock, C.; Kumarathasan, P.; Guénette, J.; Potvin, M.; Goegan, P.; Bouthillier, L.

    1997-01-01

    We have investigated the acute lung toxicity of urban particulate matter in interaction with ozone. Rats were exposed for 4 hours to clean air, ozone (0.8 ppm), the urban dust EHC-93 (5 mg/m3 or 50 mg/m3), or ozone in combination with urban dust. The animals were returned to clean air for 32 hours and then injected (intraperitoneally) with [3H]thymidine to label proliferating cells and killed after 90 minutes. The lungs were fixed by inflation, embedded in glycol methacrylate, and processed for light microscopy autoradiography. Cell labeling was low in bronchioles (0.14 +/- 0.04%) and parenchyma (0.13 +/- 0.02%) of air control animals. Inhalation of EHC-93 alone did not induce cell labeling. Ozone alone increased (P < 0.05) cell labeling (bronchioles, 0.42 +/- 0.16%; parenchyma, 0.57 +/- 0.21%), in line with an acute reparative cell proliferation. The effects of ozone were clearly potentiated by co-exposure with either the low (3.31 +/- 0.31%; 0.99 +/- 0.18%) or the high (4.45 +/- 0.51%; 1.47 +/- 0.18%) concentrations of urban dust (ozone X EHC-93, P < 0.05). Cellular changes were most notable in the epithelia of terminal bronchioles and alveolar ducts and did not distribute to the distal parenchyma. Enhanced DNA synthesis indicates that particulate matter from ambient air can exacerbate epithelial lesions in the lungs. This may extend beyond air pollutant interactions, such as to effects of inhaled particles in the lungs of compromised individuals. Images Figure 1 PMID:9403707

  3. Ambient particulate matter and lung function growth in Chinese children

    PubMed Central

    Roy, Ananya; Hu, Wei; Wei, Fusheng; Korn, Leo; Chapman, Robert S.; Zhang, Junfeng (Jim)

    2012-01-01

    Background Exposure to particulate matter (PM) has been associated with deficits in lung function growth among children in Western countries. However, few studies have explored this association in developing countries, where PM levels are often substantially higher. Methods Children (n=3273) aged 6–12 years were recruited from eight schools in four cities. The lung function parameters of forced vital capacity (FVC) and forced expiratory volume in 1 second (FEV1) were measured using computerized spirometers twice a year for up to three years (1993–1996). Dichotomous samplers placed in each schoolyard were used to measure PM2.5 and PM10 (PM with diameter ≤ 2.5 and ≤ 10, respectively). Multivariable generalized estimating equations were used to examine the association between the quarterly average PM levels and lung function growth over the period of follow-up. Results Annual average PM2.5 and PM10 levels in the four cities ranged from 57 to 158 μg/m3 and 95 to 268 μg/m3, respectively. In multivariable models, an increase of 10 μg/m3 of PM2.5 was associated with decreases of 2.7 ml FEV1 (95% confidence interval= −3.5 to −2.0), 3.5 ml FVC (−4.3 to −2.7), 1.4 ml/year FEV1 growth (−1.8 to −0.9), and 1.5 ml/year FVC growth (−2.0 to −1.0). Similar results were seen with PM10 exposure. Conclusions Exposure to ambient particulate matter was associated with decreased growth in lung function among Chinese children. PMID:22407138

  4. Trends in primary particulate matter emissions from Canadian agriculture.

    PubMed

    Pattey, Elizabeth; Qiu, Guowang

    2012-07-01

    Particulate matter (PM) has long been recognized as an air pollutant due to its adverse health and environmental impacts. As emission of PM from agricultural operations is an emerging air quality issue, the Agricultural Particulate Matter Emissions Indicator (APMEI) has been developed to estimate the primary PM contribution to the atmosphere from agricultural operations on Census years and to assess the impact of practices adopted to mitigate these emissions at the soil landscape polygon scale as part of the agri-environmental indicator report series produced by Agriculture and Agri-Food Canada. In the APMEI, PM emissions from animal feeding operations, wind erosion, land preparation, crop harvest, fertilizer and chemical application, grain handling, and pollen were calculated and compared for the Census years of 1981-2006. In this study, we present the results for PM10 and PM2.5, which exclude chemical application and pollen sources as they only contribute to total suspended particles. In 2006, PM emissions from agricultural operations were estimated to be 652.6 kt for PM10 and 158.1 kt for PM2.5. PM emissions from wind erosion and land preparation account for most of PM emissions from agricultural operations in Canada, contributing 82% of PM10 and 76% of PM2.5 in 2006. Results from the APMEI show a strong reduction in PM emissions from agricultural operations between 1981 and 2006, with a decrease of 40% (442.8 kt) for PM10 and 47% (137.7 kt) for PM2.5. This emission reduction is mainly attributed to the adoption of conservation tillage and no-till practices and the reduction in the area of summer fallow land.

  5. Comparison of methods for online measurement of diesel particulate matter.

    PubMed

    Liu, Zhun; Swanson, Jacob; Kittelson, David B; Pui, David Y H

    2012-06-05

    Gravimetric analysis is the regulatory method for diesel particulate mass measurement. Because of issues such as adsorption/volatilization artifacts, it faces obstacles in measuring ultra low level emissions from modern diesel engines. Alternative methods of suspended particle mass measurement have been developed that show improvements in time resolution, sensitivity, and accuracy. Three size-resolved methods were considered here. Two methods rely on converting number size distributions obtained using a scanning mobility particle sizer (SMPS). Conversion techniques were based on effective density measurements and the Lall-Friedlander aggregate model. The third method employs the Universal Nanoparticle Analyzer (UNPA) to measure the aggregate size distribution from which mass is calculated. Results were compared with mass concentrations obtained using gravimetric analysis. The effective density conversion resulted in mass concentrations that were highly correlated (R(2) >0.99) with filter mass. The ratios to filter mass concentration were found to be 0.99 ± 0.04, 0.45 ± 0.03, and 0.45 ± 0.19 for the effective density conversion, the Lall-Friedlander conversion, and the UNPA, respectively, for a wide range of engine operating conditions. In addition, the diesel aerosol mass distributions measured by the online techniques are in agreement to within 15-20% with respect to the mass median diameter, while discrepancies were observed in the mass concentration.

  6. Ambient particulate matter induces an exacerbation of airway inflammation in experimental asthma: role of interleukin-33.

    PubMed

    Shadie, A M; Herbert, C; Kumar, R K

    2014-08-01

    High levels of ambient environmental particulate matter (PM10 i.e. < 10 μm median aerodynamic diameter) have been linked to acute exacerbations of asthma. We examined the effects of delivering a single dose of Sydney PM10 by intranasal instillation to BALB/c mice that had been sensitized to ovalbumin and challenged repeatedly with a low (≈3 mg/m(3)) mass concentration of aerosolized ovalbumin for 4 weeks. Responses were compared to animals administered carbon black as a negative control, or a moderate (≈30 mg/m(3)) concentration of ovalbumin to simulate an allergen-induced acute exacerbation of airway inflammation. Delivery of PM10 to mice, in which experimental mild chronic asthma had previously been established, elicited characteristic features of enhanced allergic inflammation of the airways, including eosinophil and neutrophil recruitment, similar to that in the allergen-induced exacerbation. In parallel, there was increased expression of mRNA for interleukin (IL)-33 in airway tissues and an increased concentration of IL-33 in bronchoalveolar lavage fluid. Administration of a monoclonal neutralizing anti-mouse IL-33 antibody prior to delivery of particulates significantly suppressed the inflammatory response induced by Sydney PM10, as well as the levels of associated proinflammatory cytokines in lavage fluid. We conclude that IL-33 plays a key role in driving airway inflammation in this novel experimental model of an acute exacerbation of chronic allergic asthma induced by exposure to PM10.

  7. Ambient particulate matter induces an exacerbation of airway inflammation in experimental asthma: role of interleukin-33

    PubMed Central

    Shadie, A M; Herbert, C; Kumar, R K

    2014-01-01

    High levels of ambient environmental particulate matter (PM10 i.e. < 10 μm median aerodynamic diameter) have been linked to acute exacerbations of asthma. We examined the effects of delivering a single dose of Sydney PM10 by intranasal instillation to BALB/c mice that had been sensitized to ovalbumin and challenged repeatedly with a low (≈3 mg/m3) mass concentration of aerosolized ovalbumin for 4 weeks. Responses were compared to animals administered carbon black as a negative control, or a moderate (≈30 mg/m3) concentration of ovalbumin to simulate an allergen-induced acute exacerbation of airway inflammation. Delivery of PM10 to mice, in which experimental mild chronic asthma had previously been established, elicited characteristic features of enhanced allergic inflammation of the airways, including eosinophil and neutrophil recruitment, similar to that in the allergen-induced exacerbation. In parallel, there was increased expression of mRNA for interleukin (IL)-33 in airway tissues and an increased concentration of IL-33 in bronchoalveolar lavage fluid. Administration of a monoclonal neutralizing anti-mouse IL-33 antibody prior to delivery of particulates significantly suppressed the inflammatory response induced by Sydney PM10, as well as the levels of associated proinflammatory cytokines in lavage fluid. We conclude that IL-33 plays a key role in driving airway inflammation in this novel experimental model of an acute exacerbation of chronic allergic asthma induced by exposure to PM10. PMID:24730559

  8. Exposure to particulate matter in India: A synthesis of findings and future directions.

    PubMed

    Pant, Pallavi; Guttikunda, Sarath K; Peltier, Richard E

    2016-05-01

    Air pollution poses a critical threat to human health with ambient and household air pollution identified as key health risks in India. While there are many studies investigating concentration, composition, and health effects of air pollution, investigators are only beginning to focus on estimating or measuring personal exposure. Further, the relevance of exposures studies from the developed countries in developing countries is uncertain. This review summarizes existing research on exposure to particulate matter (PM) in India, identifies gaps and offers recommendations for future research. There are a limited number of studies focused on exposure to PM and/or associated health effects in India, but it is evident that levels of exposure are much higher than those reported in developed countries. Most studies have focused on coarse aerosols, with a few studies on fine aerosols. Additionally, most studies have focused on a handful of cities, and there are many unknowns in terms of ambient levels of PM as well as personal exposure. Given the high mortality burden associated with air pollution exposure in India, a deeper understanding of ambient pollutant levels as well as source strengths is crucial, both in urban and rural areas. Further, the attention needs to expand beyond the handful large cities that have been studied in detail.

  9. Fifteen-Year Global Time Series of Satellite-Derived Fine Particulate Matter

    SciTech Connect

    Boys, B. L.; Martin, R. V.; van Donkelaar, A.; MacDonell, R. J.; Hsu, N. C.; Cooper, M. J.; Yantosca, R. M.; Lu, Z.; Streets, D. G.; Zhang, Q.; Wang, S. W.

    2014-10-07

    Ambient fine particulate matter (PM2.5) is a leading environmental risk factor for premature mortality. We use aerosol optical depth (AOD) retrieved from two satellite instruments, MISR and SeaWiFS, to produce a unified 15-year global time series (1998-2012) of ground-level PM2.5 concentration at a resolution of 1 degrees x 1 degrees. The GEOS-Chem chemical transport model (CTM) is used to relate each individual AOD retrieval to ground-level PM2.5. Four broad areas showing significant, spatially coherent, annual trends are examined in detail: the Eastern U.S. (-0.39 +/- 0.10 mu g m(-3) yr(-1)), the Arabian Peninsula (0.81 +/- 0.21 mu g m(-3) yr(-1)), South Asia (0.93 +/- 0.22 mu g m(-3) yr(-1)) and East Asia (0.79 +/- 0.27 mu g m(-3) yr(-1)). Over the period of dense in situ observation (1999-2012), the linear tendency for the Eastern U.S. (-0.37 +/- 0.13 mu g m(-3) yr(-1)) agrees well with that from in situ measurements (-0.38 +/- 0.06 mu g m(-3) yr(-1)). A GEOS-Chem simulation reveals that secondary inorganic aerosols largely explain the observed PM2.5 trend over the Eastern U.S., South Asia, and East Asia, while mineral dust largely explains the observed trend over the Arabian Peninsula.

  10. Global perspective on the oxidative potential of airborne particulate matter: a synthesis of research findings.

    PubMed

    Saffari, Arian; Daher, Nancy; Shafer, Martin M; Schauer, James J; Sioutas, Constantinos

    2014-07-01

    An emerging hypothesis in the field of air pollution is that oxidative stress is one of the important pathways leading to adverse health effects of airborne particulate matter (PM). To advance our understanding of sources and chemical elements contributing to aerosol oxidative potential and provide global comparative data, we report here on the biological oxidative potential associated with size-segregated airborne PM in different urban areas of the world, measured by a biological (cell-based) reactive oxygen species (ROS) assay. Our synthesis indicates a generally greater intrinsic PM oxidative potential as well as higher levels of exposure to redox-active PM in developing areas of the world. Moreover, on the basis of our observations, smaller size fractions are generally associated with higher intrinsic ROS activity compared with larger PM size fractions. Another important outcome of our study is the identification of major species and sources that are associated with ROS activity. Water-soluble transition metals (e.g., Fe, Ni, Cu, Cr, Mn, Zn and V) and water-soluble organic carbon (WSOC) showed consistent correlations with the oxidative potential of airborne PM across different urban areas and size ranges. The major PM sources associated with these chemical species include residual/fuel oil combustion, traffic emissions, and secondary organic aerosol formation, indicating that these sources are major drivers of PM-induced oxidative potential. Moreover, comparison of ROS activity levels across different seasons indicated that photochemical aging increases the intrinsic oxidative potential of airborne PM.

  11. CHARACTERIZATION OF PARTICULATE MATTER FROM PHOENIX, ARIZONA, USING RAY FLUORESCENCE AND COMPUTER-CONTROLLED SCANNING ELECTRON MICROSCOPY

    EPA Science Inventory

    Numerous epidemiological studies have found associations between airborne particulate matter measured at community monitors and increased mortality and morbidity. Chemical and physical characteristics of particulate matter (e.g., elemental composition, size) and source identifi...

  12. Carcinogens and mutagens in ambient-air particulate matter: sources and trends in Contra Costa County. Final report

    SciTech Connect

    Flessel, P.; Guirguis, G.; Chang, K.; Cheng, J.; Lecocq, J.

    1985-06-01

    The report describes a more-sensitive method for measuring aerosol mutagens, the identification of sources of mutagens and the analysis of trends in mutagen and polycyclic aromatic hydrocarbon (PAH) levels in particulate organic matter (POM). A highly sensitive version of the Ames Salmonella test, called the microsuspension test, was applied to measure the mutagenic activity in organic extracts of community aerosols. Application of the test made possible high resolution diurnal studies of mutagenicity in air samples of only 2 hours duration. The origins of mutagens in POM were investigated during seasonal pollution episodes. Samples were analyzed for mutagenic activity, PAH, NO/sub 3//sup -1/, pollutant gases and elemental source tracers. Industrial contributions to mutagenic aerosols were suggested by significant positive correlations between mutagens and S at stations near oil refineries and chemical plants. Mutagens and PAH were also positively correlated with tracers for motor vehicles, (Br, CO) and secondary aerosols NO/sub 3//sup -1/. Routine collection and analysis of 4-month seasonal composite filter samples was carried out between 1979-1984. Levels of most pollutants, including mutagens and PAH, were highest in the winter (Nov. - Feb.). Monitoring also revealed a positive trend in the concentration of mutagenic aerosols, despite decreasing or constant levels of other pollutants including PAH.

  13. Evaluation of particulate matter abatement strategies for almond harvest.

    PubMed

    Faulkner, William B; Downey, Daniel; Giles, D Ken; Capareda, Sergio C

    2011-04-01

    Almond harvest accounts for substantial PM10 (particulate matter [PM] < or =10 microm in nominal aerodynamic diameter) emissions in California each harvest season. This paper evaluates the effects of using reduced-pass sweepers and lower harvester separation fan speeds (930 rpm) on lowering PM emissions from almond harvesting operations. In-canopy measurements of PM concentrations were collected along with PM concentration measurements at the orchard boundary; these were used in conjunction with on-site meteorological data and inverse dispersion modeling to back-calculate emission rates from the measured concentrations. The harvester discharge plume was measured as a function of visible plume opacity during conditioning operations. Reduced-pass sweeping showed the potential for reducing PM emissions, but results were confounded because of differences in orchard maturity and irrigation methods. Fuel consumption and sweeping time per unit area were reduced when comparing a reduced-pass sweeper to a conventional sweeper. Reducing the separation fan speed from 1080 to 930 rpm led to reductions in PM emissions. In general, foreign matter levels within harvested product were nominally affected by separation fan speed in the south (less mature) orchard; however, in samples conditioned using the lower fan speed from the north (more mature) orchard, these levels were unacceptable.

  14. High-efficiency particulate air filter test stand and aerosol generator for particle loading studies.

    PubMed

    Arunkumar, R; Hogancamp, Kristina U; Parsons, Michael S; Rogers, Donna M; Norton, Olin P; Nagel, Brian A; Alderman, Steven L; Waggoner, Charles A

    2007-08-01

    This manuscript describes the design, characterization, and operational range of a test stand and high-output aerosol generator developed to evaluate the performance of 30 x 30 x 29 cm(3) nuclear grade high-efficiency particulate air (HEPA) filters under variable, highly controlled conditions. The test stand system is operable at volumetric flow rates ranging from 1.5 to 12 standard m(3)/min. Relative humidity levels are controllable from 5%-90% and the temperature of the aerosol stream is variable from ambient to 150 degrees C. Test aerosols are produced through spray drying source material solutions that are introduced into a heated stainless steel evaporation chamber through an air-atomizing nozzle. Regulation of the particle size distribution of the aerosol challenge is achieved by varying source solution concentrations and through the use of a postgeneration cyclone. The aerosol generation system is unique in that it facilitates the testing of standard HEPA filters at and beyond rated media velocities by consistently providing, into a nominal flow of 7 standard m(3)/min, high mass concentrations (approximately 25 mg/m(3)) of dry aerosol streams having count mean diameters centered near the most penetrating particle size for HEPA filters (120-160 nm). Aerosol streams that have been generated and characterized include those derived from various concentrations of KCl, NaCl, and sucrose solutions. Additionally, a water insoluble aerosol stream in which the solid component is predominantly iron (III) has been produced. Multiple ports are available on the test stand for making simultaneous aerosol measurements upstream and downstream of the test filter. Types of filter performance related studies that can be performed using this test stand system include filter lifetime studies, filtering efficiency testing, media velocity testing, evaluations under high mass loading and high humidity conditions, and determination of the downstream particle size distributions.

  15. The movement of small particulate matter in the early solar system and the formation of satellites

    NASA Technical Reports Server (NTRS)

    Gold, T.

    1974-01-01

    The motions of the abundant small particulate matter in the early solar system are discussed. The effects of gas drag and resonance effects of perturbing forces could have led to accretion and differentiation of the matter. The composition of the moon and the existence of the rings of Saturn can be explained on the basis of the assembly of small particulate matter in satellite orbits around the planets.

  16. Green Ocean Amazon 2014/15 High-Volume Filter Sampling: Atmospheric Particulate Matter of an Amazon Tropical City and its Relationship to Population Health Field Campaign Report

    SciTech Connect

    Machado, C. M.; Santos, Erickson O.; Fernandes, Karenn S.; Neto, J. L.; Souza, Rodrigo A.

    2016-08-01

    Manaus, the capital of the Brazilian state of Amazonas, is developing very rapidly. Its pollution plume contains aerosols from fossil fuel combustion mainly due to vehicular emission, industrial activity, and a thermal power plant. Soil resuspension is probably a secondary source of atmospheric particles. The plume transports from Manaus to the U.S. Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) Climate Research Facility ARM site at Manacapuru urban pollutants as well as pollutants from pottery factories along the route of the plume. Considering the effects of particulate matter on health, atmospheric particulate matter was evaluated at this site as part of the ARM Facility’s Green Ocean Amazon 2014/15 (GoAmazon 2014/15) field campaign. Aerosol or particulate matter (PM) is typically defined by size, with the smaller particles having more health impact. Total suspended particulate (TSP) are particles smaller than 100 μm; particles smaller than 2.5 μm are called PM2.5. In this work, the PM2.5 levels were obtained from March to December of 2015, totaling 34 samples and TSP levels from October to December of 2015, totaling 17 samples. Sampling was conducted with PM2.5 and TSP high-volume samplers using quartz filters (Figure 1). Filters were stored during 24 hours in a room with temperature (21,1ºC) and humidity (44,3 %) control, in order to do gravimetric analyses by weighing before and after sampling. This procedure followed the recommendations of the Brazilian Association for Technical Standards local norm (NBR 9547:1997). Mass concentrations of particulate matter were obtained from the ratio between the weighted sample and the volume of air collected. Defining a relationship between particulate matter (PM2.5 and TSP) and respiratory diseases of the local population is an important goal of this project, since no information exists on that topic.

  17. Noise Pollution and How it Can Indirectly Affect the Amounts of Particulate Matter in the Environment

    NASA Astrophysics Data System (ADS)

    Swamy, S.; Power, J.; Pham, D.; Preston, K. B.; Iqbal, A.

    2007-12-01

    Human and animal activity that occurs on gravel and dirt roads tends to contribute to high levels of particulate matter in the atmosphere. Birds molt their feathers, automobiles emit unused residues, and humans and animals stir up debris on the ground. Not only do these activities generate particulate matter, but they also generate noise. The aim of our study was to determine if a direct correlation exists between the amount of particulate matter and the noise levels in select areas within the Lake Merritt Park region of downtown Oakland, California. In addition, our research was aimed at determining if the level of noise at various locations conforms to City of Oakland regulations. Over a four-week period we measured noise levels and particulate matter concentrations at 27 different sites within the Park region. Preliminary results indicate that at a construction site and a residential area near the lake a direct correlation between our two variables existed; high noise level accompanied high particulate matter while low noise level accompanied low particulate matter, respectively. However, at the majority of the areas around the lake either indirect or no correlation was observed. Based on our results thus far, we conclude that noise levels are not indicative of particulate matter levels and that noise levels around Lake Merritt do conform to the city's regulations.

  18. A study of the origin, nature, and behavior of particulate matter and metallic atoms in the mesosphere, lower thermosphere, and at the mesopause. [using lidar data

    NASA Technical Reports Server (NTRS)

    Poultney, S. K.

    1973-01-01

    In a study of particulate matter and metallic atoms in the vicinity of the mesopause, three areas have received the most effort. These areas are: the significance of cometary dust influxes to the earth's atmosphere; the relation of nightglows to atmospheric motions and aerosols; and the feasibility of using an airborne resonant scatter lidar to study polar noctilucent clouds, the sodium layer, and fireball dust.

  19. Particulate matter mass and chemical component concentrations over four Chinese cities along the western Pacific coast.

    PubMed

    Xu, Hong; Bi, Xiao-Hui; Zheng, Wei-Wei; Wu, Jian-Hui; Feng, Yin-Chang

    2015-02-01

    China has witnessed rapid economic growth in the past three decades, especially in coastal areas. Particulate matter (PM) pollution is becoming increasingly serious in China's cities along the western Pacific coast with the rapid development of China's society and economy. This study analyzed PM (PM10 and PM2.5) in terms of their mass and chemical composition in four coastal Chinese cities. The goal was to study the spatial variation and characteristics of PM pollution in sites under different levels of economic development and in diverse natural environments. A distinct trend for concentrations of PM and related chemical species was observed and increased from south to north in Haikou, Ningbo, Qingdao, and Tianjin. Secondary inorganic aerosols, crustal materials, and organic matter dominated the composition of both PM10 and PM2.5. Crustal materials were the most abundant species in the northern coastal areas because these areas have less vegetation cover and lower humidity than southern coastal areas. The presence of high SO4 (2-)/nitrate (NO3 (-)) concentrations indicated that the burning of coals gives significant contributions to PM10 and PM2.5. The differences observed in the characteristics of PM pollution in these coastal cities are probably caused by different levels of industrial and urban development.

  20. Identification and chemical characterization of industrial particulate matter sources in southwest Spain.

    PubMed

    Alastuey, Andrés; Querol, Xavier; Plana, Feliciano; Viana, Mar; Ruiz, Carmen R; Sánchez de la Campa, Ana; de la Rosa, Jesús; Mantilla, Enrique; García dos Santos, Saul

    2006-07-01

    A detailed physical and chemical characterization of coarse particulate matter (PM10) and fine particulate matter (PM2.5) in the city of Huelva (in Southwestern Spain) was carried out during 2001 and 2002. To identify the major emission sources with a significant influence on PM10 and PM2.5, a methodology was developed based on the combination of: (1) real-time measurements of levels of PM10, PM2.5, and very fine particulate matter (PM1); (2) chemical characterization and source apportionment analysis of PM10 and PM2.5; and (3) intensive measurements in field campaigns to characterize the emission plumes of several point sources. Annual means of 37, 19, and 16 microg/m3 were obtained for the study period for PM10, PM2.5, and PM1, respectively. High PM episodes, characterized by a very fine grain size distribution, are frequently detected in Huelva mainly in the winter as the result of the impact of the industrial emission plumes on the city. Chemical analysis showed that PM at Huelva is characterized by high PO4(3-) and As levels, as expected from the industrial activities. Source apportionment analyses identified a crustal source (36% of PM10 and 31% of PM2.5); a traffic-related source (33% of PM10 and 29% of PM2.5), and a marine aerosol contribution (only in PM10, 4%). In addition, two industrial emission sources were identified in PM10 and PM2.5: (1) a petrochemical source, 13% in PM10 and 8% in PM2.5; and (2) a mixed metallurgical-phosphate source, which accounts for 11-12% of PM10 and PM2.5. In PM2.5 a secondary source has been also identified, which contributed to 17% of the mass. A complete characterization of industrial emission plumes during their impact on the ground allowed for the identification of tracer species for specific point sources, such as petrochemical, metallurgic, and fertilizer and phosphate production industries.

  1. Determination of polycyclic aromatic hydrocarbons in diesel exhaust particulate matter and diesel fuel oil.

    PubMed

    Obuchi, A; Aoyama, H; Ohi, A; Ohuchi, H

    1984-11-16

    Clean-up procedures were developed for a method for determining the amount of polycyclic aromatic hydrocarbons (PAHs) in diesel exhaust particulate matter and in diesel fuel oils using reversed-phase high-performance liquid chromatography (HPLC). They were based mainly on the elimination of insoluble matter and aliphatic compounds that affect the performance of HPLC, from the dichloromethane extracts of particulate matter or from oils, with the aid of a disposable preparation column containing reversed-phase packings (Sep-Pak C18). Using these procedures, it is possible to detect 1 ng of benzo(a)pyrene in 30 mg of particulate matter with more than a 97% recovery or 0.5 ng in 50 microliters of oil with 91% recovery. Examples of analyses are given for particulate matter emitted from a diesel test engine and for diesel fuel oils, such as gas oil, residual oil and coal-liquefied oil.

  2. Organic matter of the troposphere—IV. Lipids in harmattan aerosols of nigeria

    NASA Astrophysics Data System (ADS)

    Simoneit, Bernd R. T.; Cox, R. E.; Standley, L. J.

    Harmattan aerosols were sampled during the 1979 and 1980 seasons in urban, rural and remote areas of Nigeria, in order to characterize sources of the continental carbonaceous particulate matter. High volume air samples (400-3600 m 3) were obtained. The sample filters were extracted and the soluble lipids were separated into functional group fractions for molecular analyses. These lipids were composed primarily of vascular plant wax and minor amounts of microbial detritus, with a significant anthropogenic component from petroleum products and burning superimposed in samples under urban influence. Plant wax was characterized by the homologous series of mainly n-alkanes and n-alkanols, with minor amounts of n-alkanoic acids, n-alkan-2-ones and biomarkers, all in the higher molecular weight range (> C 20). Alcohol fractions contained characteristic phytosterols (C 27-C 29) and triterpenols (C 30 > C 29), which are the biomarkers for vegetation sources. The plant wax signatures of the aerosols in northern Nigeria could be correlated with two dominant geographic source regions (e.g. northern Nigeria and Sahara). A microbial lipid component was evident primarily in the hydrocarbon (as unresolved complex mixture, UCM) and fatty acid fractions (< C 20). Its origin was inferred to be from erosion of lacustrine detritus and from viable microbiota in the ambient particles. Petroleum residues and traces of pyrogenic polynuclear aromatic hydrocarbons (PAH) were present in HC fractions of Harmattan aerosols under some urban influence. These anthropogenic components were comprised of n-alkanes (matter source determinations. This permitted the assignment of Harmattan aerosol source regions and the conclusion that the urban components are rapidly diluted

  3. Characteristics of Fine Particulate Carbonaceous Aerosol at Two Remote Sites in Central Asia

    EPA Science Inventory

    Central Asia is a relatively understudied region of the world in terms of characterizing ambient particulate matter (PM) and quantifying source impacts of PM at receptor locations, although it is speculated to have an important role as a source region for long-range transport of ...

  4. Aerosolization of Particulate (1→3)-β-d-Glucan from Moldy Materials▿

    PubMed Central

    Seo, Sung-Chul; Reponen, Tiina; Levin, Linda; Borchelt, Tiffany; Grinshpun, Sergey A.

    2008-01-01

    Mold-damaged building materials may contain biologically active agents, such as (1→3)-β-d-glucan, allergens, and mycotoxins, which have been associated with adverse health effects. The release of these components from contaminated surfaces into the air is not well understood. The purpose of this study was to characterize the release of particulate (1→3)-β-d-glucan from the surface of artificially mold-contaminated materials. Aspergillus versicolor and Stachybotrys chartarum were grown on malt extract agar (MEA), white ceiling tiles, and a wall-papered gypsum board for 1 and 6 months. The (1→3)-β-d-glucan on the surfaces of moldy materials and in air samples collected from these materials was analyzed by the Limulus amebocyte lysate assay. The aerosolization ratio was defined as the amount of (1→3)-β-d-glucan in the air divided by the amount on the surface. The results showed that the aerosolization of particulate (1→3)-β-d-glucan was influenced mainly by the type of material and the fungal species. For A. versicolor, the aerosolization ratios of particulate (1→3)-β-d-glucan released from the three types of material were not significantly different. However, the ratios for S. chartarum released from ceiling tiles and gypsum board were significantly higher than the ratios for this organism released from MEA (P < 0.001) and were comparable to those for A. versicolor. These findings indicate that the use of MEA in aerosolization experiments is likely to underestimate the release of S. chartarum particles from building materials. These results provide important background information for design of future laboratory or animal experiments, as well as for interpretation of field measurement data. PMID:18065630

  5. Inferring Atmospheric Particulate Matter Concentrations from Chinese Social Media Data

    PubMed Central

    Tao, Zhu; Kokas, Aynne; Zhang, Rui; Cohan, Daniel S.; Wallach, Dan

    2016-01-01

    Although studies have increasingly linked air pollution to specific health outcomes, less well understood is how public perceptions of air quality respond to changing pollutant levels. The growing availability of air pollution measurements and the proliferation of social media provide an opportunity to gauge public discussion of air quality conditions. In this paper, we consider particulate matter (PM) measurements from four Chinese megacities (Beijing, Shanghai, Guangzhou, and Chengdu) together with 112 million posts on Weibo (a popular Chinese microblogging system) from corresponding days in 2011–2013 to identify terms whose frequency was most correlated with PM levels. These correlations are used to construct an Air Discussion Index (ADI) for estimating daily PM based on the content of Weibo posts. In Beijing, the Chinese city with the most PM as measured by U.S. Embassy monitor stations, we found a strong correlation (R = 0.88) between the ADI and measured PM. In other Chinese cities with lower pollution levels, the correlation was weaker. Nonetheless, our results show that social media may be a useful proxy measurement for pollution, particularly when traditional measurement stations are unavailable, censored or misreported. PMID:27649530

  6. Spatial Temporal Modelling of Particulate Matter for Health Effects Studies

    NASA Astrophysics Data System (ADS)

    Hamm, N. A. S.

    2016-10-01

    Epidemiological studies of the health effects of air pollution require estimation of individual exposure. It is not possible to obtain measurements at all relevant locations so it is necessary to predict at these space-time locations, either on the basis of dispersion from emission sources or by interpolating observations. This study used data obtained from a low-cost sensor network of 32 air quality monitoring stations in the Dutch city of Eindhoven, which make up the ILM (innovative air (quality) measurement system). These stations currently provide PM10 and PM2.5 (particulate matter less than 10 and 2.5 m in diameter), aggregated to hourly means. The data provide an unprecedented level of spatial and temporal detail for a city of this size. Despite these benefits the time series of measurements is characterized by missing values and noisy values. In this paper a space-time analysis is presented that is based on a dynamic model for the temporal component and a Gaussian process geostatistical for the spatial component. Spatial-temporal variability was dominated by the temporal component, although the spatial variability was also substantial. The model delivered accurate predictions for both isolated missing values and 24-hour periods of missing values (RMSE = 1.4 μg m-3 and 1.8 μg m-3 respectively). Outliers could be detected by comparison to the 95% prediction interval. The model shows promise for predicting missing values, outlier detection and for mapping to support health impact studies.

  7. Decomposition of N2O over particulate matter

    NASA Technical Reports Server (NTRS)

    Rebbert, R. E.; Ausloos, P.

    1978-01-01

    Nitrous oxide is shown to undergo both a thermal and a photochemical decomposition at 296 K when it is adsorbed on various dry sands. The photochemical process occurs with light of wavelengths greater than 280 nm, where gaseous N2O does not absorb. At low pressures (less than 0.1 torr) the half-life for the thermal decomposition of nitrous oxide to nitrogen when placed in contact with about 5 gm of heat-treated Tunisian sand in a one-liter vessel was 350 + or - 35 days. Under certain photolytic conditions this half-life was reduced. The efficiency of the photolytic process for a particular sand depends on the pressure and on the wavelength of light. For Tunisian sand at 1.1 torr and with the full mercury arc, the destruction efficiency is about 0.00002 molecule/incident photon. These results indicate that particulate matter in the troposphere may be responsible for the decomposition of nitrous oxide and hence act as an atmospheric sink for N2O. However, moisture causes a drastic reduction in the number of molecules dissociated per incident photon.

  8. Protein oxidation and degradation caused by particulate matter

    PubMed Central

    Lai, Ching-Huang; Lee, Chun-Nin; Bai, Kuan-Jen; Yang, You-Lan; Chuang, Kai-Jen; Wu, Sheng-Ming; Chuang, Hsiao-Chi

    2016-01-01

    Particulate matter (PM) modulates the expression of autophagy; however, the role of selective autophagy by PM remains unclear. The objective of this study was to determine the underlying mechanisms in protein oxidation and degradation caused by PM. Human epithelial A549 cells were exposed to diesel exhaust particles (DEPs), urban dust (UD), and carbon black (CB; control particles). Cell survival and proliferation were significantly reduced by DEPs and UD in A549 cells. First, benzo(a)pyrene diolepoxide (BPDE) protein adduct was caused by DEPs at 150 μg/ml. Methionine oxidation (MetO) of human albumin proteins was induced by DEPs, UD, and CB; however, the protein repair mechanism that converts MetO back to methionine by methionine sulfoxide reductases A (MSRA) and B3 (MSRB3) was activated by DEPs and inhibited by UD, suggesting that oxidized protein was accumulating in cells. As to the degradation of oxidized proteins, proteasome and autophagy activation was induced by CB with ubiquitin accumulation, whereas proteasome and autophagy activation was induced by DEPs without ubiquitin accumulation. The results suggest that CB-induced protein degradation may be via an ubiquitin-dependent autophagy pathway, whereas DEP-induced protein degradation may be via an ubiquitin-independent autophagy pathway. A distinct proteotoxic effect may depend on the physicochemistry of PM. PMID:27644844

  9. Monitoring of airborne particulate matter at mountainous urban sites.

    PubMed

    Dai, Jun; Kim, Ki-Hyun; Dutta, Tanushree; Park, Wha Me; Hong, Jong-Ki; Jung, Kweon; Brown, Richard J C

    2016-08-01

    Concentrations of various size fractions (TSP, PM10, PM2.5, and PM1.0) of particulate matter (PM) were measured at two mountainous sites, Buk Han (BH) and Gwan AK (GA), along with one ground reference site at Gwang Jin (GJ), located in Seoul, South Korea for the 4 years from 2010 to 2013. The daily average concentrations of TSP, PM10, PM2.5, and PM1.0 at BH were 47.9 ± 32.5, 37.0 ± 24.6, 20.6 ± 12.9, and 15.3 ± 9.53 μg m(-3), respectively. These values were slightly larger than those measured at GA while much lower than those measured at the reference site (GJ). Seasonal variations in PM concentrations were consistent across all locations with a relative increase in concentrations observed in spring and winter. Correlation analysis showed clear differences in PM concentrations between the mountainous sites and the reference site. Analysis of these PM concentrations indicated that the distribution of PM in the mountainous locations was affected by a number of manmade sources from nearby locations, including both traffic and industrial emissions.

  10. Improvements in PIXE analysis of hourly particulate matter samples

    NASA Astrophysics Data System (ADS)

    Calzolai, G.; Lucarelli, F.; Chiari, M.; Nava, S.; Giannoni, M.; Carraresi, L.; Prati, P.; Vecchi, R.

    2015-11-01

    Most air quality studies on particulate matter (PM) are based on 24-h averaged data; however, many PM emissions as well as their atmospheric dilution processes change within a few hours. Samplings of PM with 1-h resolution can be performed by the streaker sampler (PIXE International Corporation), which is designed to separate the fine (aerodynamic diameter less than 2.5 μm) and the coarse (aerodynamic diameter between 2.5 and 10 μm) fractions of PM. These samples are efficiently analyzed by Particle Induced X-ray Emission (PIXE) at the LABEC laboratory of INFN in Florence (Italy), equipped with a 3 MV Tandetron accelerator, thanks to an optimized external-beam set-up, a convenient choice of the beam energy and suitable collecting substrates. A detailed description of the adopted set-up and results from a methodological study on the detection limits for the selection of the optimal beam energy are shown; the outcomes of the research on alternative collecting substrates, which produce a lower background during the measurements, and with lower contaminations, are also discussed.

  11. Air Pollution Particulate Matter Alters Antimycobacterial Respiratory Epithelium Innate Immunity

    PubMed Central

    Rivas-Santiago, César E.; Sarkar, Srijata; Cantarella, Pasquale; Osornio-Vargas, Álvaro; Quintana-Belmares, Raúl; Meng, Qingyu; Kirn, Thomas J.; Ohman Strickland, Pamela; Chow, Judith C.; Watson, John G.; Torres, Martha

    2015-01-01

    Inhalation exposure to indoor air pollutants and cigarette smoke increases the risk of developing tuberculosis (TB). Whether exposure to ambient air pollution particulate matter (PM) alters protective human host immune responses against Mycobacterium tuberculosis has been little studied. Here, we examined the effect of PM from Iztapalapa, a municipality of Mexico City, with aerodynamic diameters below 2.5 μm (PM2.5) and 10 μm (PM10) on innate antimycobacterial immune responses in human alveolar type II epithelial cells of the A549 cell line. Exposure to PM2.5 or PM10 deregulated the ability of the A549 cells to express the antimicrobial peptides human β-defensin 2 (HBD-2) and HBD-3 upon infection with M. tuberculosis and increased intracellular M. tuberculosis growth (as measured by CFU count). The observed modulation of antibacterial responsiveness by PM exposure was associated with the induction of senescence in PM-exposed A549 cells and was unrelated to PM-mediated loss of cell viability. Thus, the induction of senescence and downregulation of HBD-2 and HBD-3 expression in respiratory PM-exposed epithelial cells leading to enhanced M. tuberculosis growth represent mechanisms by which exposure to air pollution PM may increase the risk of M. tuberculosis infection and the development of TB. PMID:25847963

  12. Epigenetic Alterations Induced by Ambient Particulate Matter in Mouse Macrophages

    PubMed Central

    Miousse, Isabelle R.; Chalbot, Marie-Cécile G.; Aykin-Burns, Nükhet; Wang, Xiaoying; Basnakian, Alexei; Kavouras, Ilias G.; Koturbash, Igor

    2014-01-01

    Respiratory mortality and morbidity has been associated with exposure to particulate matter (PM). Experimental evidence suggests involvement of cytotoxicity, oxidative stress, and inflammation in the development of PM-associated pathological states; however, the exact mechanisms remain unclear. In the current study, we analyzed short-term epigenetic response to PM10 (particles with aerodynamic diameter less than 10 μm) exposure in mouse ascitic RAW264.7 macrophages (BALB/C Abelson murine leukemia virus-induced tumor). Ambient PM10 was collected using a high volume sampler in Little Rock, AR. Analysis revealed that PM10 was composed mainly of Al and Fe, and the water soluble organic fraction was dominated by aliphatic and carbohydrate fragments and minor quantities of aromatic components. Exposure to PM10 compromised the cellular epigenome at concentrations 10–200 μg/ml. Specifically, epigenetic alterations were evident as changes in the methylation and expression of repetitive element-associated DNA and associated DNA methylation machinery. These results suggest that epigenetic alterations, in concert with cytotoxicity, oxidative stress, and inflammation, might contribute to the pathogenesis of PM-associated respiratory diseases. PMID:24535919

  13. Magnetic quantification of urban pollution sources in atmospheric particulate matter

    NASA Astrophysics Data System (ADS)

    Spassov, S.; Egli, R.; Heller, F.; Nourgaliev, D. K.; Hannam, J.

    2004-11-01

    A new method is presented for fast quantification of urban pollution sources in atmospheric particulate matter (PM). The remanent magnetization of PM samples collected in Switzerland at sites with different exposures to pollution sources is analysed. The coercivity distribution of each sample is calculated from detailed demagnetization curves of anhysteretic remanent magnetization (ARM) and is modelled using a linear combination of appropriate functions which represent the contribution of different sources of magnetic minerals to the total magnetization. Two magnetic components, C1 and C2, are identified in all samples. The low-coercivity component C1 predominates in less polluted sites, whereas the concentration of the higher-coercivity component C2 is large in urban areas. The same sites were monitored independently by Hüglin using detailed chemical analysis and a quantitative source attribution of the PM. His results are compared with the magnetic component analysis. The absolute and relative magnetic contributions of component C2 correlate very well with absolute and relative mass contributions of exhaust emissions, respectively. Traffic is the most important PM pollution source in Switzerland: it includes exhaust emissions and abrasion products released by vehicle brakes. Component C2 and traffic-related PM sources correlate well, which is encouraging for the implementation of non-destructive magnetic methods as an economic alternative to chemical analysis when mapping urban dust pollution.

  14. Modeling residential fine particulate matter infiltration for exposure assessment.

    PubMed

    Hystad, Perry U; Setton, Eleanor M; Allen, Ryan W; Keller, Peter C; Brauer, Michael

    2009-09-01

    Individuals spend the majority of their time indoors; therefore, estimating infiltration of outdoor-generated fine particulate matter (PM(2.5)) can help reduce exposure misclassification in epidemiological studies. As indoor measurements in individual homes are not feasible in large epidemiological studies, we evaluated the potential of using readily available data to predict infiltration of ambient PM(2.5) into residences. Indoor and outdoor light scattering measurements were collected for 84 homes in Seattle, Washington, USA, and Victoria, British Columbia, Canada, to estimate residential infiltration efficiencies. Meteorological variables and spatial property assessment data (SPAD), containing detailed housing characteristics for individual residences, were compiled for both study areas using a geographic information system. Multiple linear regression was used to construct models of infiltration based on these data. Heating (October to February) and non-heating (March to September) season accounted for 36% of the yearly variation in detached residential infiltration. Two SPAD housing characteristic variables, low building value, and heating with forced air, predicted 37% of the variation found between detached residential infiltration during the heating season. The final model, incorporating temperature and the two SPAD housing characteristic variables, with a seasonal interaction term, explained 54% of detached residential infiltration. Residences with low building values had higher infiltration efficiencies than other residences, which could lead to greater exposure gradients between low and high socioeconomic status individuals than previously identified using only ambient PM(2.5) concentrations. This modeling approach holds promise for incorporating infiltration efficiencies into large epidemiology studies, thereby reducing exposure misclassification.

  15. Skin Damage Mechanisms Related to Airborne Particulate Matter Exposure.

    PubMed

    Magnani, Natalia D; Muresan, Ximena M; Belmonte, Giuseppe; Cervellati, Franco; Sticozzi, Claudia; Pecorelli, Alessandra; Miracco, Clelia; Marchini, Timoteo; Evelson, Pablo; Valacchi, Giuseppe

    2016-01-01

    Epidemiological studies suggest a correlation between increased airborne particulate matter (PM) and adverse health effects. The mechanisms of PM-health effects are believed to involve oxidative stress and inflammation. To evaluate the ability of PM promoting skin tissue damage, one of the main organs exposed to outdoor pollutants, we analyzed the effect of concentrated ambient particles (CAPs) in a reconstructed human epidermis (RHE) model. RHE tissues were exposed to 25 or 100 µg/ml CAPs for 24 or 48 h. Data showed that RHE seems to be more susceptible to CAPs-induced toxicity after 48 h exposure than after 24 h. We found a local reactive O(2) species (ROS) production increase generated from metals present on the particle, which contributes to lipids oxidation. Furthermore, as a consequence of altered redox status, NFkB nucleus translocation was increase upon CAPs exposure, as well as cyclooxygenase 2 and cytochrome P450 levels, which may be involved in the inflammatory response initiated by PM. CAPs also triggered an apoptotic process in skin. Surprisingly, by transition electron microscopy analysis we showed that CAPs were able to penetrate skin tissues. These findings contribute to the understanding of the cutaneous pathophysiological mechanisms initiated by CAPs exposure, where oxidative stress and inflammation may play predominant roles.

  16. Particulate matter and heart disease: Evidence from epidemiological studies

    SciTech Connect

    Peters, Annette . E-mail: peters@gsf.de

    2005-09-01

    The association between particulate matter and heart disease was noted in the mid-nineties of last century when the epidemiological evidence for an association between air pollution and hospital admissions due to cardiovascular disease accumulated and first hypotheses regarding the pathomechanism were formulated. Nowadays, epidemiological studies have demonstrated coherent associations between daily changes in concentrations of ambient particles and cardiovascular disease mortality, hospital admission, disease exacerbation in patients with cardiovascular disease and early physiological responses in healthy individuals consistent with a risk factor profile deterioration. In addition, evidence was found that annual average PM{sub 2.5} exposures are associated with increased risks for mortality caused by ischemic heart disease and dysrhythmia. Thereby, evidence is suggesting not only a short-term exacerbation of cardiovascular disease by ambient particle concentrations but also a potential role of particles in defining patients' vulnerability to acute coronary events. While this concept is consistent with the current understanding of the factors defining patients' vulnerability, the mechanisms and the time-scales on which the particle-induced vulnerability might operate are unknown.

  17. The environmental cost of reducing agricultural fine particulate matter emissions.

    PubMed

    Funk, Paul A

    2010-06-01

    The U.S. Environmental Protection Agency (EPA) revised the National Ambient Air Quality Standards (NAAQS) in 2006, reducing acceptable fine particulate matter (PM2.5) levels; state environmental protection agencies in states with nonattainment areas are required to draft State Implementation Plans (SIPs) detailing measures to reduce regional PM2.5 levels by reducing PM2.5 and PM2.5 precursor emissions. These plans need to account for increases in emissions caused by operating control technologies. Potential PM2.5 emissions reductions realized by adding a second set of dust cyclones were estimated for the cotton ginning industry. Increases in energy consumption were calculated based on dust cyclone air pressure drop. Additional energy required was translated into increased emissions using published emission factors and state emissions inventories. Reductions in gin emissions were compared with increases in emissions at the power plant. Because of the electrical energy required, reducing one unit of agricultural PM2.5 emissions at a cotton gin results in emitting 0.11-2.67 units of direct PM2.5, 1.39-69.1 units of PM2.5 precursors, 1.70-76.8 units of criteria pollutants, and 692-15,400 units of greenhouse gases at the point where electricity is produced. If regulations designed to reduce rural PM2.5 emissions increase electrical power consumption, the unintended net effect may be more emissions, increased environmental damage, and a greater risk to public health.

  18. Foam cell formation by particulate matter (PM) exposure: a review.

    PubMed

    Cao, Yi; Long, Jimin; Ji, Yuejia; Chen, Gui; Shen, Yuexin; Gong, Yu; Li, Juan

    2016-11-01

    Increasing evidence suggests that exposure of particulate matter (PM) from traffic vehicles, e.g., diesel exhaust particles (DEP), was associated with adverse vascular effects, e.g., acceleration of atherosclerotic plaque progression. By analogy, engineered nanoparticles (NPs) could also induce similar effects. The formation of lipid laden foam cells, derived predominately from macrophages and vascular smooth muscle cells (VSMC), is closely associated with the development of atherosclerosis and adverse vascular effects. We reviewed current studies about particle exposure-induced lipid laden foam cell formation. In vivo studies using animal models have shown that exposure of air pollution by PM promoted lipid accumulation in alveolar macrophages or foam cells in plaques, which was likely associated with pulmonary inflammation or systemic oxidative stress, but not blood lipid profile. In support of these findings, in vitro studies showed that direct exposure of cultured macrophages to DEP or NP exposure, with or without further exposure to external lipids, promoted intracellular lipid accumulation. The mechanisms remained unknown. Although a number studies found increased reactive oxygen species (ROS) or an adaptive response to oxidative stress, the exact role of oxidative stress in mediating particle-induced foam cell formation requires future research. There is currently lack of reports concerning VSMC as a source for foam cells induced by particle exposure. In the future, it is necessary to explore the role of foam cell formation in particle exposure-induced atherosclerosis development. In addition, the formation of VSMC derived foam cells by particle exposure may also need extensive studies.

  19. Airborne endotoxin in fine particulate matter in Beijing

    NASA Astrophysics Data System (ADS)

    Guan, Tianjia; Yao, Maosheng; Wang, Junxia; Fang, Yanhua; Hu, Songhe; Wang, Yan; Dutta, Anindita; Yang, Junnan; Wu, Yusheng; Hu, Min; Zhu, Tong

    2014-11-01

    Endotoxin is an important biological component of particulate matter (PM) which, upon inhalation, can induce adverse health effects, and also possibly complicate the diseases in combination with other pollutants. From 1 March 2012 to 27 February 2013 we collected air samples using quartz filters daily for the quantification of airborne endotoxin and also fine PM (PM2.5) in Beijing, China. The geometric means for endotoxin concentration and the fraction of endotoxin in PM were 0.65 EU/m3 (range: 0.10-75.02) and 10.25 EU/mg PM2.5 (range: 0.38-1627.29), respectively. The endotoxin concentrations were shown to vary greatly with seasons, typically with high values in the spring and winter seasons. Temperature and relative humidity, as well as concentrations of sulfur dioxide and nitrogen oxides were found to be significantly correlated with airborne endotoxin concentrations (p < 0.05). Additionally, positive correlations were also detected between endotoxin concentrations and natural sources of Na+, K+, Mg2+, and F-, while negative correlations were observed between endotoxin concentrations and anthropogenic sources of P, Co, Zn, As, and Tl. Oxidative potential analysis revealed that endotoxin concentrations were positively correlated with reactive oxygen species (ROS), but not dithiothreitol (DTT) of PM. This study provided the first continuous time series of airborne endotoxin concentrations in Beijing, and identifies its potential associations with atmospheric factors. The information developed here can assist in the assessment of health effects of air pollution in Beijing.

  20. Protein oxidation and degradation caused by particulate matter

    NASA Astrophysics Data System (ADS)

    Lai, Ching-Huang; Lee, Chun-Nin; Bai, Kuan-Jen; Yang, You-Lan; Chuang, Kai-Jen; Wu, Sheng-Ming; Chuang, Hsiao-Chi

    2016-09-01

    Particulate matter (PM) modulates the expression of autophagy; however, the role of selective autophagy by PM remains unclear. The objective of this study was to determine the underlying mechanisms in protein oxidation and degradation caused by PM. Human epithelial A549 cells were exposed to diesel exhaust particles (DEPs), urban dust (UD), and carbon black (CB; control particles). Cell survival and proliferation were significantly reduced by DEPs and UD in A549 cells. First, benzo(a)pyrene diolepoxide (BPDE) protein adduct was caused by DEPs at 150 μg/ml. Methionine oxidation (MetO) of human albumin proteins was induced by DEPs, UD, and CB; however, the protein repair mechanism that converts MetO back to methionine by methionine sulfoxide reductases A (MSRA) and B3 (MSRB3) was activated by DEPs and inhibited by UD, suggesting that oxidized protein was accumulating in cells. As to the degradation of oxidized proteins, proteasome and autophagy activation was induced by CB with ubiquitin accumulation, whereas proteasome and autophagy activation was induced by DEPs without ubiquitin accumulation. The results suggest that CB-induced protein degradation may be via an ubiquitin-dependent autophagy pathway, whereas DEP-induced protein degradation may be via an ubiquitin-independent autophagy pathway. A distinct proteotoxic effect may depend on the physicochemistry of PM.