Origin and Distribution of PAHs in Ambient Particulate Samples at High Mountain Region in Southern China

Directory of Open Access Journals (Sweden)

Peng-hui Li

2015-01-01

Full Text Available To understand the deposition and transport of PAHs in southern China, a measurement campaign was conducted at a high-elevation site (the summit of Mount Heng, 1269 m A.S.L. from April 4 to May 31, 2009, and a total of 39 total suspended particulate samples were collected for measurement of PAH concentrations. The observed particulate-bound PAHs concentrations ranged from 1.63 to 29.83 ng/m3, with a mean concentration of 6.03 ng/m3. BbF, FLA, and PYR were the predominant compounds. Good correlations were found between individual PAHs and meteorological parameters such as atmospheric pressure, relative humidity, and ambient temperature. The backward trajectory analysis suggested that particulate samples measured at the Mount Heng region were predominantly associated with the air masses from southern China, while the air masses transported over northern and northwestern China had relative higher PAHs concentrations. Based on the diagnostic ratios and factor analysis, vehicular emission, coal combustion, industry emission, and unburned fossil fuels were suggested to be the PAHs sources at Mount Heng site. However, the reactivity and degradation of individual PAHs could influence the results of PAH source profiles, which deserves further investigations in the future.

Source contributions and regional transport of primary particulate matter in China

International Nuclear Information System (INIS)

Hu, Jianlin; Wu, Li; Zheng, Bo; Zhang, Qiang; He, Kebin; Chang, Qing; Li, Xinghua; Yang, Fumo; Ying, Qi; Zhang, Hongliang

2015-01-01

A source-oriented CMAQ was applied to determine source sector/region contributions to primary particulate matter (PPM) in China. Four months were simulated with emissions grouped to eight regions and six sectors. Predicted elemental carbon (EC), primary organic carbon (POC), and PPM concentrations and source contributions agree with measurements and have significant spatiotemporal variations. Residential is a major contributor to spring/winter EC (50–80%), POC (60%–90%), and PPM (30–70%). For summer/fall, industrial contributes 30–50% for EC/POC and 40–60% for PPM. Transportation is more important for EC (20–30%) than POC/PPM ( 90% in Beijing. - Highlights: • A source-oriented CMAQ was established for primary particulate matter (PPM). • Source and region contributions to EC, POC and PPM in China were quantified. • Residential is major in spring/winter and industrial dominates in summer/fall. • Open burning is more important for southern while dust is in contrast. • Both local and Heibei emissions contribute to PPM in Beijing. - Source and region contributions to primary particulate matter in China were quantified for four months during 2012-2013. Residential and industrial are the major contributors.

Assessment of Contribution of Contemporary Carbon Sources to Size-Fractionated Particulate Matter and Time-Resolved Bulk Particulate Matter Using the Measurement of Radiocarbon

Energy Technology Data Exchange (ETDEWEB)

Hwang, H M; Young, T M; Buchholz, B A

2009-04-16

This study was motivated by a desire to improve understanding of the sources contributing to the carbon that is an important component of airborne particulate matter (PM). The ultimate goal of this project was to lay a ground work for future tools that might be easily implemented with archived or routinely collected samples. A key feature of this study was application of radiocarbon measurement that can be interpreted to indicate the relative contributions from fossil and non-fossil carbon sources of atmospheric PM. Size-resolved PM and time-resolved PM{sub 10} collected from a site in Sacramento, CA in November 2007 (Phase I) and March 2008 (Phase II) were analyzed for radiocarbon and source markers such as levoglucosan, cholesterol, and elemental carbon. Radiocarbon data indicates that the contributions of non-fossil carbon sources were much greater than that from fossil carbon sources in all samples. Radiocarbon and source marker measurements confirm that a greater contribution of non-fossil carbon sources in Phase I samples was highly likely due to residential wood combustion. The present study proves that measurement of radiocarbon and source markers can be readily applied to archived or routinely collected samples for better characterization of PM sources. More accurate source apportionment will support ARB in developing more efficient control strategies.

Magnesium, Iron and Aluminum in LLNL Air Particulate and Rain Samples with Reference to Magnesium in Industrial Storm Water

Energy Technology Data Exchange (ETDEWEB)

Esser, Bradley K. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Bibby, Richard K. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Fish, Craig [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

2016-08-25

Storm water runoff from the Lawrence Livermore National Laboratory’s (LLNL’s) main site and Site 300 periodically exceeds the Discharge Permit Numeric Action Level (NAL) for Magnesium (Mg) under the Industrial General Permit (IGP) Order No. 2014-0057-DWQ. Of particular interest is the source of magnesium in storm water runoff from the site. This special study compares new metals data from air particulate and precipitation samples from the LLNL main site and Site 300 to previous metals data for storm water from the main site and Site 300 and alluvial sediment from the main site to investigate the potential source of elevated Mg in storm water runoff. Data for three metals (Mg, Iron {Fe}, and Aluminum {Al}) were available from all media; data for additional metals, such as Europium (Eu), were available from rain, air particulates, and alluvial sediment. To attribute source, this study compared metals concentration data (for Mg, Al, and Fe) in storm water and rain; metal-metal correlations (Mg with Fe, Mg with Al, Al with Fe, Mg with Eu, Eu with Fe, and Eu with Al) in storm water, rain, air particulates, and sediments; and metal-metal ratios ((Mg/Fe, Mg/Al, Al/Fe, Mg/Eu, Eu/Fe, and Eu/Al) in storm water, rain, air particulates and sediments. The results presented in this study are consistent with a simple conceptual model where the source of Mg in storm water runoff is air particulate matter that has dry-deposited on impervious surfaces and subsequently entrained in runoff during precipitation events. Such a conceptual model is consistent with 1) higher concentrations of metals in storm water runoff than in precipitation, 2) the strong correlation of Mg with Aluminum (Al) and Iron (Fe) in both storm water and air particulates, and 3) the similarity in metal mass ratios between storm water and air particulates in contrast to the dissimilarity of metal mass ratios between storm water and precipitation or alluvial sediment. The strong correlation of Mg with Fe and Al

Observations of fine particulate nitrated phenols in four sites in northern China: concentrations, source apportionment, and secondary formation

Science.gov (United States)

Wang, Liwei; Wang, Xinfeng; Gu, Rongrong; Wang, Hao; Yao, Lan; Wen, Liang; Zhu, Fanping; Wang, Weihao; Xue, Likun; Yang, Lingxiao; Lu, Keding; Chen, Jianmin; Wang, Tao; Zhang, Yuanghang; Wang, Wenxing

2018-03-01

Filter samples of fine particulate matters were collected at four sites in northern China (urban, rural, and mountain) in summer and winter, and the contents of nine nitrated phenols were quantified in the laboratory with the use of ultra-high-performance liquid chromatography coupled with mass spectrometry. During the sampling periods, the concentrations of particulate nitrated phenols exhibited distinct temporal and spatial variation. On average, the total concentration of particulate nitrated phenols in urban Jinan in the wintertime reached 48.4 ng m-3, and those in the summertime were 9.8, 5.7, 5.9, and 2.5 ng m-3 in urban Jinan, rural Yucheng and Wangdu, and Mt. Tai, respectively. The elevated concentrations of nitrated phenols in wintertime and in urban areas demonstrate the apparent influences of anthropogenic sources. The positive matrix factorization receptor model was then applied to determine the origins of particulate nitrated phenols in northern China. The five major source factors were traffic, coal combustion, biomass burning, secondary formation, and aged coal combustion plume. Among them, coal combustion played a vital role, especially at the urban site in the wintertime, with a contribution of around 55 %. In the summertime, the observed nitrated phenols were highly influenced by aged coal combustion plumes at all of the sampling sites. Meanwhile, in remote areas, contributions from secondary formation were significant. Further correlation analysis indicates that nitrosalicylic acids were produced mostly from secondary formation that was dominated by NO2 nitration.

Establishment of a Practical Approach for Characterizing the Source of Particulates in Water Distribution Systems

Directory of Open Access Journals (Sweden)

Seon-Ha Chae

2016-02-01

Full Text Available Water quality complaints related to particulate matter and discolored water can be troublesome for water utilities in terms of follow-up investigations and implementation of appropriate actions because particulate matter can enter from a variety of sources; moreover, physicochemical processes can affect the water quality during the purification and transportation processes. The origin of particulates can be attributed to sources such as background organic/inorganic materials from water sources, water treatment plants, water distribution pipelines that have deteriorated, and rehabilitation activities in the water distribution systems. In this study, a practical method is proposed for tracing particulate sources. The method entails collecting information related to hydraulic, water quality, and structural conditions, employing a network flow-path model, and establishing a database of physicochemical properties for tubercles and slimes. The proposed method was implemented within two city water distribution systems that were located in Korea. These applications were conducted to demonstrate the practical applicability of the method for providing solutions to customer complaints. The results of the field studies indicated that the proposed method would be feasible for investigating the sources of particulates and for preparing appropriate action plans for complaints related to particulate matter.

Source profiles of particulate matter emissions from a pilot-scale boiler burning North American coal blends.

Science.gov (United States)

Lee, S W

2001-11-01

Recent awareness of suspected adverse health effects from ambient particulate matter (PM) emission has prompted publication of new standards for fine PM with aerodynamic diameter less than 2.5 microm (PM2.5). However, scientific data on fine PM emissions from various point sources and their characteristics are very limited. Source apportionment methods are applied to identify contributions of individual regional sources to tropospheric particulate concentrations. The existing industrial database developed using traditional source measurement techniques provides total emission rates only, with no details on chemical nature or size characteristics of particulates. This database is inadequate, in current form, to address source-receptor relationships. A source dilution system was developed for sampling and characterization of total PM, PM2.5, and PM10 (i.e., PM with aerodynamic diameter less than 10 pm) from residual oil and coal combustion. This new system has automatic control capabilities for key parameters, such as relative humidity (RH), temperature, and sample dilution. During optimization of the prototype equipment, three North American coal blends were burned using a 0.7-megawatt thermal (MWt) pulverized coal-fired, pilot-scale boiler. Characteristic emission profiles, including PM2.5 and total PM soluble acids, and elemental and carbon concentrations for three coal blends are presented. Preliminary results indicate that volatile trace elements such as Pb, Zn, Ti, and Se are preferentially enriched in PM2.5. PM2.5 is also more concentrated in soluble sulfates relative to total PM. Coal fly ash collected at the outlet of the electrostatic precipitator (ESP) contains about 85-90% PM10 and 30-50% PM2.5. Particles contain the highest elemental concentrations of Si and Al while Ca, Fe, Na, Ba, and K also exist as major elements. Approximately 4-12% of the materials exists as soluble sulfates in fly ash generated by coal blends containing 0.2-0.8% sulfur by mass

Observations of fine particulate nitrated phenols in four sites in northern China: concentrations, source apportionment, and secondary formation

Directory of Open Access Journals (Sweden)

L. Wang

2018-03-01

Full Text Available Filter samples of fine particulate matters were collected at four sites in northern China (urban, rural, and mountain in summer and winter, and the contents of nine nitrated phenols were quantified in the laboratory with the use of ultra-high-performance liquid chromatography coupled with mass spectrometry. During the sampling periods, the concentrations of particulate nitrated phenols exhibited distinct temporal and spatial variation. On average, the total concentration of particulate nitrated phenols in urban Jinan in the wintertime reached 48.4 ng m−3, and those in the summertime were 9.8, 5.7, 5.9, and 2.5 ng m−3 in urban Jinan, rural Yucheng and Wangdu, and Mt. Tai, respectively. The elevated concentrations of nitrated phenols in wintertime and in urban areas demonstrate the apparent influences of anthropogenic sources. The positive matrix factorization receptor model was then applied to determine the origins of particulate nitrated phenols in northern China. The five major source factors were traffic, coal combustion, biomass burning, secondary formation, and aged coal combustion plume. Among them, coal combustion played a vital role, especially at the urban site in the wintertime, with a contribution of around 55 %. In the summertime, the observed nitrated phenols were highly influenced by aged coal combustion plumes at all of the sampling sites. Meanwhile, in remote areas, contributions from secondary formation were significant. Further correlation analysis indicates that nitrosalicylic acids were produced mostly from secondary formation that was dominated by NO2 nitration.

Characterization and sources of air particulate matter at Kwabenya, near Accra, Ghana

International Nuclear Information System (INIS)

Aboh, I. J. K.

2009-01-01

Gravimetric, reflectometric and elemental analyses have been carried out on airborne particulate matter sampled in a semi-rural area of Kwabenya, near Accra-Ghana. The PM 10 aerosols were sampled using a Gent sampler, size segregating the aerosol into coarse (PM 10-2.5 ) and fine (PM 1.5 ) fractions. The data and derived information were generated from 216 days of sampling spanning a period of about 14 months, 28 th December 2005 to 12 th February 2007. The particulate matter (PM) at Kwabenya was dominated by the coarse particulates and showed low levels during the Rainy season and high levels during the Harmattan period. The levels measured during the 2006/07 Harmattan were very high. The mass concentration for the measuring period were in the following ranges; coarse (PM 10-2.5 ) fraction (0.16 - 1794.01 µg/m 3 ); PM 2.5 (fine) fraction (0.50 - 430.23 µg/m 3 ) and PM 10 (0.87 µg/m 3 to 2064.89 µg/m 3 ). Additional information about the ambient air was obtained through the subsequent determination of elemental concentration using energy dispersive x-ray fluorescence (EDXRF) analysis and black carbon (BC) concentration through the b lack smoke method . The elements identified and quantified with the Quantitative X-ray Analysis System (QXAS) package software were: AI, Si, S, CI, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Br, Rb, Sr and Pb in the coarse fraction. The following elements were identified and quantified in the fine fraction: AI, Si, S, K, Ca, Ti, Mn, Fe, Cu, Zn, Br, Rb, Sr and Pb. Validation of the quantitative methods with the standard reference filter SRM2783 gave very good agreement (within ± 15%) for most elements analysed except for Ni (±43%)which was very close to the detection limit. The elemental concentrations in the two fractions vary from season to season. Using simple correlation analysis some elements correlate, the elemental correlations also vary from season to season, for example during the Harmattan S, CI, V, Br and Sr correlated very

Bioaccessibility and Speciation of Potential Toxicants in Some Geogenic Sources of Atmospheric Particulate Matter

Science.gov (United States)

Morman, S. A.; Wolf, R. E.; Plumlee, G.; Reynolds, R. L.

2008-12-01

The correlation of exposure to particulate matter (PM) and increased morbidity and mortality was established in the 1970's. Research focused on elucidating mechanisms of action (i.e. particle size, composition, and biodurability), has generally examined anthropogenic sources such as solid or liquid combustion byproducts of fossil fuels, byproducts from the smelting of metal ores, and commercial/industrial mineral dusts (asbestos, crystalline silica. metal dusts). While many studies exist on agricultural exposures to inorganic dust, far fewer have examined health issues related to particulate matter contributions from rural, non-agricultural dusts or other geogenic sources. Geogenic PM (produced by natural processes such as volcanic ash, volcanic fog (vog), dusts from dry lakes or glacial deposits, smoke and windborne ash from wildfires, and dusts containing various soil pathogens) and geoanthropogenic PM (produced from natural sources by processes that are modified or enhanced by human activities such as dusts from lakebeds dried by human removal of water, dusts produced from areas that have undergone desertification as a result of human practices etc.) are increasingly recognized as potential agents of toxicity and disease, via both environmental and occupational exposures. Surface sediment on some dry lake beds may contribute significant amounts of mineral dusts to the atmospheric load. For example, Owens Lake (a dry lake in southern California) has been a major source of PM10 (particulate matter less than 10 micrometers) dust in the United States. Dusts from dry and drying saline lakes may contain high concentrations of metals, such as arsenic, with known human health toxicity. Wildfires, consuming over nine million acres in 2007, also contribute significant amounts of particulate matter in addition to their other hazards. Designed to estimate the bioaccessibility of metals in soils, dusts and other environmental materials by measuring the reactivity of the

Chemical characteristics and source apportionment of fine particulate organic carbon in Hong Kong during high particulate matter episodes in winter 2003

Science.gov (United States)

Li, Yun-Chun; Yu, Jian Zhen; Ho, Steven Sai Hang; Schauer, James J.; Yuan, Zibing; Lau, Alexis K. H.; Louie, Peter K. K.

2013-02-01

PM2.5 samples were collected at six general stations and one roadside station in Hong Kong in two periods of high particulate matter (PM) in 2003 (27 October-4 November and 30 November-13 December). The highest PM2.5 reached 216 μg m- 3 during the first high PM period and 113 μg m- 3 during the second high PM period. Analysis of synoptic weather conditions identified individual sampling days under dominant influence of one of three types of air masses, that is, local, regional and long-range transported (LRT) air masses. Roadside samples were discussed separately due to heavy influences from vehicular emissions. This research examines source apportionment of fine organic carbon (OC) and contribution of secondary organic aerosol on high PM days under different synoptic conditions. Six primary OC (POC) sources (vehicle exhaust, biomass burning, cooking, cigarette smoke, vegetative detritus, and coal combustion) were identified on the basis of characteristic organic tracers. Individual POC source contributions were estimated using chemical mass balance model. In the roadside and the local samples, OC was dominated by the primary sources, accounting for more than 74% of OC. In the samples influenced by regional and LRT air masses, secondary OC (SOC), which was approximated to be the difference between the total measured OC and the apportioned POC, contributed more than 54% of fine OC. SOC was highly correlated with water-soluble organic carbon and sulfate, consistent with its secondary nature.

Characteristics of thin and coarse particulates of urban and natural brazilian aerosols

International Nuclear Information System (INIS)

Orsini, C.Q.; Tabacnics, M.H.; Artaxo, P.; Andrade, M.F.; Kerr, A.S.

1994-01-01

Thin and coarse particulate were sampled during the period 1982-1985 in a natural coastal forest (Jureia), and five urban-industrial regions (Vitoria, Salvador, Porto Alegre, Sao Paulo and Belo Horizonte). The time variation of the concentration in the air, and the relative elementary composition of the thin and coarse particulate, sampled by thin and Coarse Particulate Sampler (AFG), were determined by gravimetric method and PIXE analysis respectively. The results demonstrated that the ground dust and salt from the sea are unequivocally one of the largest sources of coarse particulate, and also the ground is a significant thin particulate source. 25 refs, 22 figs, 28 tabs. (L.C.J.A.)

Particulate organic nitrates: Sampling and night/day variation

DEFF Research Database (Denmark)

Nielsen, T.; Platz, J.; Granby, K.

1998-01-01

Atmospheric day and night concentrations of particulate organic nitrates (PON) and several other air pollutants were measured in the summer 1995 over an open-land area in Denmark. The sampling of PON was evaluated comparing 24 h samples with two sets of 12 h samples. These results indicate...... that the observed low contribution of PON to NO, is real and not the result of an extensive loss during the sampling. Empirical relationships between the vapour pressure and chemical formula of organic compounds were established in order to evaluate the gas/particle distribution of organic nitrates. A positive...

Particulate pollutants in the Brazilian city of São Paulo: 1-year investigation for the chemical composition and source apportionment

Science.gov (United States)

Martins Pereira, Guilherme; Teinilä, Kimmo; Custódio, Danilo; Gomes Santos, Aldenor; Xian, Huang; Hillamo, Risto; Alves, Célia A.; Bittencourt de Andrade, Jailson; Olímpio da Rocha, Gisele; Kumar, Prashant; Balasubramanian, Rajasekhar; de Fátima Andrade, Maria; de Castro Vasconcellos, Pérola

2017-10-01

São Paulo in Brazil has relatively relaxed regulations for ambient air pollution standards and often experiences high air pollution levels due to emissions of particulate pollutants from local sources and long-range transport of air masses impacted by biomass burning. In order to evaluate the sources of particulate air pollution and related health risks, a year-round sampling was done at the University of São Paulo campus (20 m a.g.l.), a green area near an important expressway. The sampling was performed for PM2. 5 ( ≤ 2. 5 µm) and PM10 ( ≤ 10 µm) in 2014 through intensive (everyday sampling in wintertime) and extensive campaigns (once a week for the whole year) with 24 h of sampling. This year was characterized by having lower average precipitation compared to meteorological data, and high-pollution episodes were observed all year round, with a significant increase in pollution level in the intensive campaign, which was performed during wintertime. Different chemical constituents, such as carbonaceous species, polycyclic aromatic hydrocarbons (PAHs) and derivatives, water-soluble ions, and biomass burning tracers were identified in order to evaluate health risks and to apportion sources. The species such as PAHs, inorganic and organic ions, and monosaccharides were determined using chromatographic techniques and carbonaceous species using thermal-optical analysis. Trace elements were determined using inductively coupled plasma mass spectrometry. The risks associated with particulate matter exposure based on PAH concentrations were also assessed, along with indexes such as the benzo[a]pyrene equivalent (BaPE) and lung cancer risk (LCR). High BaPE and LCR were observed in most of the samples, rising to critical values in the wintertime. Also, biomass burning tracers and PAHs were higher in this season, while secondarily formed ions presented low variation throughout the year. Meanwhile, vehicular tracer species were also higher in the intensive campaign

Particulate pollutants in the Brazilian city of São Paulo: 1-year investigation for the chemical composition and source apportionment

Directory of Open Access Journals (Sweden)

G. M. Pereira

2017-10-01

Full Text Available São Paulo in Brazil has relatively relaxed regulations for ambient air pollution standards and often experiences high air pollution levels due to emissions of particulate pollutants from local sources and long-range transport of air masses impacted by biomass burning. In order to evaluate the sources of particulate air pollution and related health risks, a year-round sampling was done at the University of São Paulo campus (20 m a.g.l., a green area near an important expressway. The sampling was performed for PM2. 5 ( ≤ 2. 5 µm and PM10 ( ≤  10 µm in 2014 through intensive (everyday sampling in wintertime and extensive campaigns (once a week for the whole year with 24 h of sampling. This year was characterized by having lower average precipitation compared to meteorological data, and high-pollution episodes were observed all year round, with a significant increase in pollution level in the intensive campaign, which was performed during wintertime. Different chemical constituents, such as carbonaceous species, polycyclic aromatic hydrocarbons (PAHs and derivatives, water-soluble ions, and biomass burning tracers were identified in order to evaluate health risks and to apportion sources. The species such as PAHs, inorganic and organic ions, and monosaccharides were determined using chromatographic techniques and carbonaceous species using thermal-optical analysis. Trace elements were determined using inductively coupled plasma mass spectrometry. The risks associated with particulate matter exposure based on PAH concentrations were also assessed, along with indexes such as the benzo[a]pyrene equivalent (BaPE and lung cancer risk (LCR. High BaPE and LCR were observed in most of the samples, rising to critical values in the wintertime. Also, biomass burning tracers and PAHs were higher in this season, while secondarily formed ions presented low variation throughout the year. Meanwhile, vehicular tracer species were also

Computation of radionuclide particulate finite area fugitive source strengths

Energy Technology Data Exchange (ETDEWEB)

Fields, D E

1983-06-01

Atmospheric source strengths quantifying particulate re-suspension from wind and non-wind disturbance-driven processes are computed for sites of small area. These values are useful in computing downwind air concentration values to evaluate risk to exposed populations. The net source strength for the site is the sum of the wind- and disturbance-driven components. A unified source strength approach includes both classes of re-suspension processes. More research is needed to satisfactorily express the time-dependence of re-suspension parameters, especially in non-arid climates where population densities are greater. (JMT)

Impact of fugitive sources and meteorological parameters on vertical distribution of particulate matter over the industrial agglomeration.

Science.gov (United States)

Štrbová, Kristína; Raclavská, Helena; Bílek, Jiří

2017-12-01

The aim of the study was to characterize vertical distribution of particulate matter, in an area well known by highest air pollution levels in Europe. A balloon filled with helium with measuring instrumentation was used for vertical observation of air pollution over the fugitive sources in Moravian-Silesian metropolitan area during spring and summer. Synchronously, selected meteorological parameters were recorded together with particulate matter for exploration its relationship with particulate matter. Concentrations of particulate matter in the vertical profile were significantly higher in the spring than in the summer. Significant effect of fugitive sources was observed up to the altitude ∼255 m (∼45 m above ground) in both seasons. The presence of inversion layer was observed at the altitude ∼350 m (120-135 m above ground) at locations with major source traffic load. Both particulate matter concentrations and number of particles for the selected particle sizes decreased with increasing height. Strong correlation of particulate matter with meteorological parameters was not observed. The study represents the first attempt to assess the vertical profile over the fugitive emission sources - old environmental burdens in industrial region. Copyright © 2017 Elsevier Ltd. All rights reserved.

Determination of mercury in airborne particulate matter collected on glass fiber filters using high-resolution continuum source graphite furnace atomic absorption spectrometry and direct solid sampling

Energy Technology Data Exchange (ETDEWEB)

Araujo, Rennan G.O., E-mail: rgoa01@terra.com.br [Laboratorio de Quimica Analitica Ambiental, Departamento de Quimica, Universidade Federal de Sergipe, Campus Sao Cristovao, 49.100-000, Sao Cristovao, SE (Brazil); Departamento de Quimica, Universidade Federal de Santa Catarina, 88040-900, Florianopolis, SC (Brazil); Vignola, Fabiola; Castilho, Ivan N.B. [Departamento de Quimica, Universidade Federal de Santa Catarina, 88040-900, Florianopolis, SC (Brazil); Borges, Daniel L.G.; Welz, Bernhard [Departamento de Quimica, Universidade Federal de Santa Catarina, 88040-900, Florianopolis, SC (Brazil); Instituto Nacional de Ciencia e Tecnologia do CNPq, INCT de Energia e Ambiente, Universidade Federal da Bahia, 40170-115 Salvador, BA (Brazil); Vale, Maria Goreti R. [Instituto Nacional de Ciencia e Tecnologia do CNPq, INCT de Energia e Ambiente, Universidade Federal da Bahia, 40170-115 Salvador, BA (Brazil); Instituto de Quimica, Universidade Federal do Rio Grande do Sul, 91501-970 Porto Alegre, RS (Brazil); Smichowski, Patricia [Comision Nacional de Energia Atomica (CNEA) and Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET), Buenos Aires (Argentina); Ferreira, Sergio L.C. [Instituto Nacional de Ciencia e Tecnologia do CNPq, INCT de Energia e Ambiente, Universidade Federal da Bahia, 40170-115 Salvador, BA (Brazil); Instituto de Quimica, Universidade Federal da Bahia, 40170-290, Salvador, BA (Brazil); Becker-Ross, Helmut [Leibniz-Institut fuer Analytische Wissenschaften-ISAS-e.V., Department Berlin, 12489 Berlin (Germany)

2011-05-15

A study has been undertaken to assess the capability of high-resolution continuum source graphite furnace atomic absorption spectrometry for the determination of mercury in airborne particulate matter (APM) collected on glass fiber filters using direct solid sampling. The main Hg absorption line at 253.652 nm was used for all determinations. The certified reference material NIST SRM 1648 (Urban Particulate Matter) was used to check the accuracy of the method, and good agreement was obtained between published and determined values. The characteristic mass was 22 pg Hg. The limit of detection (3{sigma}), based on ten atomizations of an unexposed filter, was 40 ng g{sup -1}, corresponding to 0.12 ng m{sup -3} in the air for a typical air volume of 1440 m{sup 3} collected within 24 h. The limit of quantification was 150 ng g{sup -1}, equivalent to 0.41 ng m{sup -3} in the air. The repeatability of measurements was better than 17% RSD (n = 5). Mercury concentrations found in filter samples loaded with APM collected in Buenos Aires, Argentina, were between < 40 ng g{sup -1} and 381 {+-} 24 ng g{sup -1}. These values correspond to a mercury concentration in the air between < 0.12 ng m{sup -3} and 1.47 {+-} 0.09 ng m{sup -3}. The proposed procedure was found to be simple, fast and reliable, and suitable as a screening procedure for the determination of mercury in APM samples.

Elemental analysis of size-fractionated particulate matter sampled in Goeteborg, Sweden

Energy Technology Data Exchange (ETDEWEB)

Wagner, Annemarie [Department of Chemistry, Atmospheric Science, Goeteborg University, SE-412 96 Goeteborg (Sweden)], E-mail: wagnera@chalmers.se; Boman, Johan [Department of Chemistry, Atmospheric Science, Goeteborg University, SE-412 96 Goeteborg (Sweden); Gatari, Michael J. [Institute of Nuclear Science and Technology, University of Nairobi, P.O. Box 30197-00100, Nairobi (Kenya)

2008-12-15

The aim of the study was to investigate the mass distribution of trace elements in aerosol samples collected in the urban area of Goeteborg, Sweden, with special focus on the impact of different air masses and anthropogenic activities. Three measurement campaigns were conducted during December 2006 and January 2007. A PIXE cascade impactor was used to collect particulate matter in 9 size fractions ranging from 16 to 0.06 {mu}m aerodynamic diameter. Polished quartz carriers were chosen as collection substrates for the subsequent direct analysis by TXRF. To investigate the sources of the analyzed air masses, backward trajectories were calculated. Our results showed that diurnal sampling was sufficient to investigate the mass distribution for Br, Ca, Cl, Cu, Fe, K, Sr and Zn, whereas a 5-day sampling period resulted in additional information on mass distribution for Cr and S. Unimodal mass distributions were found in the study area for the elements Ca, Cl, Fe and Zn, whereas the distributions for Br, Cu, Cr, K, Ni and S were bimodal, indicating high temperature processes as source of the submicron particle components. The measurement period including the New Year firework activities showed both an extensive increase in concentrations as well as a shift to the submicron range for K and Sr, elements that are typically found in fireworks. Further research is required to validate the quantification of trace elements directly collected on sample carriers.

Elemental analysis of size-fractionated particulate matter sampled in Goeteborg, Sweden

International Nuclear Information System (INIS)

Wagner, Annemarie; Boman, Johan; Gatari, Michael J.

2008-01-01

The aim of the study was to investigate the mass distribution of trace elements in aerosol samples collected in the urban area of Goeteborg, Sweden, with special focus on the impact of different air masses and anthropogenic activities. Three measurement campaigns were conducted during December 2006 and January 2007. A PIXE cascade impactor was used to collect particulate matter in 9 size fractions ranging from 16 to 0.06 μm aerodynamic diameter. Polished quartz carriers were chosen as collection substrates for the subsequent direct analysis by TXRF. To investigate the sources of the analyzed air masses, backward trajectories were calculated. Our results showed that diurnal sampling was sufficient to investigate the mass distribution for Br, Ca, Cl, Cu, Fe, K, Sr and Zn, whereas a 5-day sampling period resulted in additional information on mass distribution for Cr and S. Unimodal mass distributions were found in the study area for the elements Ca, Cl, Fe and Zn, whereas the distributions for Br, Cu, Cr, K, Ni and S were bimodal, indicating high temperature processes as source of the submicron particle components. The measurement period including the New Year firework activities showed both an extensive increase in concentrations as well as a shift to the submicron range for K and Sr, elements that are typically found in fireworks. Further research is required to validate the quantification of trace elements directly collected on sample carriers

Particulate matter mass concentrations produced from pavement surface abrasion

Directory of Open Access Journals (Sweden)

Fullova Dasa

2017-01-01

Full Text Available According to the latest findings particulate matter belong to the most significant pollutants in Europe together with ground-level ozone O3 and nitrogen dioxide NO2. Road traffic is one of the main sources of particulate matter. Traffic volume has unpleasant impact on longevity of the pavements and also on the environment. Vehicle motions cause mechanical wearing of the asphalt pavement surface - wearing course by vehicle tyres. The paper deals with abrasion of bituminous wearing courses of pavements. The asphalt mixtures 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 paper 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.

Identification and chemical characterization of industrial particulate matter sources in southwest Spain.

Science.gov (United States)

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.

On the autarchic use of solely PIXE data in particulate matter source apportionment studies by receptor modeling

Energy Technology Data Exchange (ETDEWEB)

Lucarelli, F. [Department of Physics and Astronomy, University of Florence, Via G. Sansone 1, 50019 Sesto Fiorentino (Italy); National Institute of Nuclear Physics (INFN)-Florence, Via G. Sansone 1, 50019 Sesto Fiorentino (Italy); Nava, S., E-mail: nava@fi.infn.it [National Institute of Nuclear Physics (INFN)-Florence, Via G. Sansone 1, 50019 Sesto Fiorentino (Italy); Calzolai, G. [Department of Physics and Astronomy, University of Florence, Via G. Sansone 1, 50019 Sesto Fiorentino (Italy); Chiari, M. [National Institute of Nuclear Physics (INFN)-Florence, Via G. Sansone 1, 50019 Sesto Fiorentino (Italy); Giannoni, M.; Traversi, R.; Udisti, R. [Department of Chemistry, University of Florence, Via della Lastruccia 3, 50019 Sesto Fiorentino (Italy)

2015-11-15

Particle Induced X-ray Emission (PIXE) analysis of aerosol samples allows simultaneous detection of several elements, including important tracers of many particulate matter sources. This capability, together with the possibility of analyzing a high number of samples in very short times, makes PIXE a very effective tool for source apportionment studies by receptor modeling. However, important aerosol components, like nitrates, OC and EC, cannot be assessed by PIXE: this limitation may strongly compromise the results of a source apportionment study if based on PIXE data alone. In this work, an experimental dataset characterised by an extended chemical speciation (elements, EC–OC, ions) is used to test the effect of reducing input species in the application of one of the most widely used receptor model, namely Positive Matrix Factorization (PMF). The main effect of using only PIXE data is that the secondary nitrate source is not identified and the contribution of biomass burning is overestimated, probably due to the similar seasonal pattern of these two sources.

Characterization of particulate emissions from Australian open-cut coal mines: Toward improved emission estimates.

Science.gov (United States)

Richardson, Claire; Rutherford, Shannon; Agranovski, Igor

2018-06-01

Given the significance of mining as a source of particulates, accurate characterization of emissions is important for the development of appropriate emission estimation techniques for use in modeling predictions and to inform regulatory decisions. The currently available emission estimation methods for Australian open-cut coal mines relate primarily to total suspended particulates and PM 10 (particulate matter with an aerodynamic diameter available relating to the PM 2.5 (currently available emission estimation techniques, this paper presents results of sampling completed at three open-cut coal mines in Australia. The monitoring data demonstrate that the particulate size fraction varies for different mining activities, and that the region in which the mine is located influences the characteristics of the particulates emitted to the atmosphere. The proportion of fine particulates in the sample increased with distance from the source, with the coarse fraction being a more significant proportion of total suspended particulates close to the source of emissions. In terms of particulate composition, the results demonstrate that the particulate emissions are predominantly sourced from naturally occurring geological material, and coal comprises less than 13% of the overall emissions. The size fractionation exhibited by the sampling data sets is similar to that adopted in current Australian emission estimation methods but differs from the size fractionation presented in the U.S. Environmental Protection Agency methodology. Development of region-specific emission estimation techniques for PM 10 and PM 2.5 from open-cut coal mines is necessary to allow accurate prediction of particulate emissions to inform regulatory decisions and for use in modeling predictions. Development of region-specific emission estimation techniques for PM 10 and PM 2.5 from open-cut coal mines is necessary to allow accurate prediction of particulate emissions to inform regulatory decisions and for

PIXE Analysis and source identification of airborne particulate matter collected in Downtown Havana City

International Nuclear Information System (INIS)

Perez, G.; Pinnera, I; Ramos, M; Guibert, R; Molina, E.; Martinez, M.; Fernandez, A.; Aldape, F.; Flores, M.

2009-01-01

A set of samples containing airborne particulate matter (in two particle size fraction PM10 and PM2,5) collected during five months from November 2006 to April 2007 in a urban area of Havana City were analyzed by Particle-Induced X-ray Emission (PIXE) technique and the concentrations of 14 elements (S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Br and Pb) were determined consistently in both particle size fractions with minimum detection limits in the range of ng/m3. A Gent air sampler was used for the aerosol collection in PM10 and PM2,5 particles simultaneously and the PIXE elemental analysis were performed using a proton beam of 2.5 MeV from the 2 MV Van de Graff Tandetron Accelerator at the ININ PIXE Laboratory in Mexico. The analytical database provided by PIXE was statistically analyzed in order to determine the promising local pollution sources. The statistical techniques of Multivariate Factor Analysis in combination with the Principal Component Analysis methods were applied to this data and allowed identifying five main pollution sources of airborne particulate matter (PM10 and PM2,5) collected in this area. The main (local) identified sources were: soil dust, sea spray, industry, fossil fuel combustion from motor vehicles and burnings or incinerations of diverse materials. A general discussion about these results is presented in this work. (Author)

Elemental analysis of air particulate samples in Jakarta area by x-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Yumiarti; Yusuf, M.; Mellawati, June; Menry, Yulizon; Surtipanti S

1998-01-01

Determination of elements in air particulate samples collected from Jakarta, especially from industrial area Pulo Gadung, also from residence, office, and recreation sites had been carried out. The samples collected periodically from August through December 1996. The elements were analyzed by X-ray fluorescence spectrometry method. Quantitative and qualitative analyses were done using QXAS AXIL (Quantitative X-ray Analysis System of x-ray Spectra by Iterative Least squares fitting) and QAES (Quantitative Analyses of Environmental Samples) package program. Results of the analyses showed that the content of heavy metal elements in air particulate samples from all areas studied were still below the maximum permissible concentration. (authors)

Fine particulates over South Asia: Review and meta-analysis of PM2.5 source apportionment through receptor model.

Science.gov (United States)

Singh, Nandita; Murari, Vishnu; Kumar, Manish; Barman, S C; Banerjee, Tirthankar

2017-04-01

Fine particulates (PM 2.5 ) constitute dominant proportion of airborne particulates and have been often associated with human health disorders, changes in regional climate, hydrological cycle and more recently to food security. Intrinsic properties of particulates are direct function of sources. This initiates the necessity of conducting a comprehensive review on PM 2.5 sources over South Asia which in turn may be valuable to develop strategies for emission control. Particulate source apportionment (SA) through receptor models is one of the existing tool to quantify contribution of particulate sources. Review of 51 SA studies were performed of which 48 (94%) were appeared within a span of 2007-2016. Almost half of SA studies (55%) were found concentrated over few typical urban stations (Delhi, Dhaka, Mumbai, Agra and Lahore). Due to lack of local particulate source profile and emission inventory, positive matrix factorization and principal component analysis (62% of studies) were the primary choices, followed by chemical mass balance (CMB, 18%). Metallic species were most regularly used as source tracers while use of organic molecular markers and gas-to-particle conversion were minimum. Among all the SA sites, vehicular emissions (mean ± sd: 37 ± 20%) emerged as most dominating PM 2.5 source followed by industrial emissions (23 ± 16%), secondary aerosols (22 ± 12%) and natural sources (20 ± 15%). Vehicular emissions (39 ± 24%) also identified as dominating source for highly polluted sites (PM 2.5 >100 μgm -3 , n = 15) while site specific influence of either or in combination of industrial, secondary aerosols and natural sources were recognized. Source specific trends were considerably varied in terms of region and seasonality. Both natural and industrial sources were most influential over Pakistan and Afghanistan while over Indo-Gangetic plain, vehicular, natural and industrial emissions appeared dominant. Influence of vehicular emission was

Identification and characterization of fine and coarse particulate matter sources in a middle-European urban environment

International Nuclear Information System (INIS)

Kertesz, Zs.; Szoboszlai, Z.; Angyal, A.; Dobos, E.; Borbely-Kiss, I.

2010-01-01

In this work a source apportionment study is presented which aimed to characterize the PM 2.5 and PM 2.5-10 sources in the urban area of Debrecen, East-Hungary by using streaker samples, IBA methods and positive matrix factorization (PMF) analysis. Samples of fine (PM 2.5 ) and coarse (PM 2.5-10 ) urban particulate matter were collected with 2 h time resolution in the frame of five sampling campaigns during 2007-2009 in different seasons in the downtown of Debrecen. Elemental concentrations from Al to Pb of over 1000 samples were obtained by particle induced X-ray emission (PIXE); concentrations of black carbon (BC) were determined with a smoke stain reflectometer. On this data base source apportionment was carried out by using the PMF method. Seven factors were identified for both size fractions, including soil dust, traffic, secondary aerosol - sulphates, domestic heating, oil combustion, agriculture and an unknown factor enriched with chlorine. Seasonal and daily variation of the different factors was studied as well as their dependence on meteorological parameters. Besides determining the time patterns characteristic to the city, several emission episodes were identified including a Saharan dust intrusion on 21st-24th May, 2008.

High-resolution sampling and analysis of ambient particulate matter in the Pearl River Delta region of southern China: source apportionment and health risk implications

Science.gov (United States)

Zhou, Shengzhen; Davy, Perry K.; Huang, Minjuan; Duan, Jingbo; Wang, Xuemei; Fan, Qi; Chang, Ming; Liu, Yiming; Chen, Weihua; Xie, Shanju; Ancelet, Travis; Trompetter, William J.

2018-02-01

Hazardous air pollutants, such as trace elements in particulate matter (PM), are known or highly suspected to cause detrimental effects on human health. To understand the sources and associated risks of PM to human health, hourly time-integrated major trace elements in size-segregated coarse (PM2.5-10) and fine (PM2.5) particulate matter were collected at the industrial city of Foshan in the Pearl River Delta region, China. Receptor modeling of the data set by positive matrix factorization (PMF) was used to identify six sources contributing to PM2.5 and PM10 concentrations at the site. Dominant sources included industrial coal combustion, secondary inorganic aerosol, motor vehicles and construction dust along with two intermittent sources (biomass combustion and marine aerosol). The biomass combustion source was found to be a significant contributor to peak PM2.5 episodes along with motor vehicles and industrial coal combustion. Conditional probability function (CPF) analysis was applied to estimate the source locations using the PMF-resolved source contribution coupled with the surface wind direction data. Health exposure risk of hazardous trace elements (Pb, As, Si, Cr, Mn and Ni) and source-specific values were estimated. The total hazard quotient (HQ) of PM2.5 was 2.09, higher than the acceptable limit (HQ = 1). The total carcinogenic risk (CR) was 3.37 × 10-3 for PM2.5, which was 3 times higher than the least stringent limit (1.0 × 10-4). Among the selected trace elements, As and Pb posed the highest non-carcinogenic and carcinogenic risks to human health, respectively. In addition, our results show that the industrial coal combustion source is the dominant non-carcinogenic and carcinogenic risk contributor, highlighting the need for stringent control of this source. This study provides new insight for policy makers to prioritize sources in air quality management and health risk reduction.

[Sample preparation methods for chromatographic analysis of organic components in atmospheric particulate matter].

Science.gov (United States)

Hao, Liang; Wu, Dapeng; Guan, Yafeng

2014-09-01

The determination of organic composition in atmospheric particulate matter (PM) is of great importance in understanding how PM affects human health, environment, climate, and ecosystem. Organic components are also the scientific basis for emission source tracking, PM regulation and risk management. Therefore, the molecular characterization of the organic fraction of PM has become one of the priority research issues in the field of environmental analysis. Due to the extreme complexity of PM samples, chromatographic methods have been the chief selection. The common procedure for the analysis of organic components in PM includes several steps: sample collection on the fiber filters, sample preparation (transform the sample into a form suitable for chromatographic analysis), analysis by chromatographic methods. Among these steps, the sample preparation methods will largely determine the throughput and the data quality. Solvent extraction methods followed by sample pretreatment (e. g. pre-separation, derivatization, pre-concentration) have long been used for PM sample analysis, and thermal desorption methods have also mainly focused on the non-polar organic component analysis in PM. In this paper, the sample preparation methods prior to chromatographic analysis of organic components in PM are reviewed comprehensively, and the corresponding merits and limitations of each method are also briefly discussed.

Monitoring of PM10 and PM2.5 around primary particulate anthropogenic emission sources

Science.gov (United States)

Querol, Xavier; Alastuey, Andrés; Rodriguez, Sergio; Plana, Felicià; Mantilla, Enrique; Ruiz, Carmen R.

Investigations on the monitoring of ambient air levels of atmospheric particulates were developed around a large source of primary anthropogenic particulate emissions: the industrial ceramic area in the province of Castelló (Eastern Spain). Although these primary particulate emissions have a coarse grain-size distribution, the atmospheric transport dominated by the breeze circulation accounts for a grain-size segregation, which results in ambient air particles occurring mainly in the 2.5-10 μm range. The chemical composition of the ceramic particulate emissions is very similar to the crustal end-member but the use of high Al, Ti and Fe as tracer elements as well as a peculiar grain-size distribution in the insoluble major phases allow us to identify the ceramic input in the bulk particulate matter. PM2.5 instead of PM10 monitoring may avoid the interference of crustal particles without a major reduction in the secondary anthropogenic load, with the exception of nitrate. However, a methodology based in PM2.5 measurement alone is not adequate for monitoring the impact of primary particulate emissions (such as ceramic emissions) on air quality, since the major ambient air particles derived from these emissions are mainly in the range of 2.5-10 μm. Consequently, in areas characterised by major secondary particulate emissions, PM2.5 monitoring should detect anthropogenic particulate pollutants without crustal particulate interference, whereas PM10 measurements should be used in areas with major primary anthropogenic particulate emissions.

Screening of various diesel particulate matter samples from various commodity mines

CSIR Research Space (South Africa)

Mahlangu, Vusi J

2016-09-01

Full Text Available This paper presents qualitative analysis results of diesel particulate matter (DPM) from various mining commodities in South Africa. The objective of this work was to determine the concentrations of elements in DPM samples. For this screening...

Particulate Matter Emission Factors for Biomass Combustion

Directory of Open Access Journals (Sweden)

Simone Simões Amaral

2016-10-01

Full Text Available Emission factor is a relative measure and can be used to estimate emissions from multiple sources of air pollution. For this reason, data from literature on particulate matter emission factors from different types of biomass were evaluated in this paper. Initially, the main sources of particles were described, as well as relevant concepts associated with particle measurements. In addition, articles about particle emissions were classified and described in relation to the sampling environment (open or closed and type of burned biomass (agricultural, garden, forest, and dung. Based on this analysis, a set of emission factors was presented and discussed. Important observations were made about the main emission sources of particulate matter. Combustion of compacted biomass resulted in lower particulate emission factors. PM2.5 emissions were predominant in the burning of forest biomass. Emission factors were more elevated in laboratory burning, followed by burns in the field, residences and combustors.

Standard Practice for Sampling for Particulate Contamination by Tape Lift

CERN Document Server

American Society for Testing and Materials. Philadelphia

2006-01-01

1.1 This practice covers procedures for sampling surfaces to determine the presence of particulate contamination, 5 m and larger. The practice consists of the application of a pressure-sensitive tape to the surface followed by the removal of particulate contamination with the removal of the tape. The tape with the adhering particles is then mounted on counting slides. Counting and measuring of particles is done by standard techniques. 1.2 This practice describes the materials and equipment required to perform sampling of surfaces for particle counting and sizing. 1.3 The criteria for acceptance or rejection of a part for conformance to surface cleanliness level requirements shall be determined by the user and are not included in this practice. 1.4 This practice is for use on surfaces that are not damaged by the application of adhesive tape. The use of this practice on any surface of any material not previously tested or for which the susceptibility to damage is unknown is not recommended. In general, metal...

Laboratory Measurements of Particulate Matter Concentrations from Asphalt Pavement Abrasion

Directory of Open Access Journals (Sweden)

Fullová Daša

2016-12-01

Full Text Available 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.

High-resolution sampling and analysis of air particulate matter in the Pear River Delta region of Southern China: source apportionment and health risk assessment

Science.gov (United States)

Zhou, S.; Day, P. K.; Wang, X.

2017-12-01

Hazardous air pollutants, such as trace elements in particulate matters (PM), are known or highly suspected to cause detrimental effects on human health. To understand the sources and associated risks of PM to human health, hourly time-integrated major trace elements in size-segregated coarse (PM10-2.5) and fine (PM2.5) particulate matter were collected and examined in an industrial city of Foshan in the Pearl River Delta region, China. Receptor modeling of the dataset by positive matrix factorization (PMF) was used to identify six sources contributing to PM2.5 and PM10 concentrations at the site. Dominant sources included industrial coal combustion, secondary inorganic aerosol, motor vehicles and construction dust along with two intermittent sources, biomass combustion and marine aerosol. The biomass combustion source was found to be a significant contributor to peak PM2.5 episodes along with motor vehicles and industrial coal combustion. Conditional probability function (CPF) was applied to estimate the local source effects from wind direction using the PMF-resolved source contribution coupled with the surface wind direction data. Health exposure risk for hazardous trace elements (Pb, As, Cr, Ni, Zn, V, Cu, Mn, Fe) and source-specific values were estimated. The total hazard quotient (total HQ =HI) of PM2.5 was 2.09, which is two times higher than the acceptable limit (HQ = 1). The total carcinogenic risk was 3.37*10-3 for PM2.5, which was three orders higher than the acceptable limit (i.e. 1.0*10-6). Among the selected trace elements, As and Pb posed the highest non-carcinogenic and carcinogenic risks for human health, respectively. In additional, our results showed that industrial coal combustion source was the dominant non-carcinogenic and carcinogenic risks contributor, highlighting the need for stringent control of this source. This study can provide new insight for policy makers to prioritize sources in air quality management and health risk reduction.

High-resolution sampling and analysis of ambient particulate matter in the Pearl River Delta region of southern China: source apportionment and health risk implications

Directory of Open Access Journals (Sweden)

S. Zhou

2018-02-01

Full Text Available Hazardous air pollutants, such as trace elements in particulate matter (PM, are known or highly suspected to cause detrimental effects on human health. To understand the sources and associated risks of PM to human health, hourly time-integrated major trace elements in size-segregated coarse (PM2.5–10 and fine (PM2.5 particulate matter were collected at the industrial city of Foshan in the Pearl River Delta region, China. Receptor modeling of the data set by positive matrix factorization (PMF was used to identify six sources contributing to PM2.5 and PM10 concentrations at the site. Dominant sources included industrial coal combustion, secondary inorganic aerosol, motor vehicles and construction dust along with two intermittent sources (biomass combustion and marine aerosol. The biomass combustion source was found to be a significant contributor to peak PM2.5 episodes along with motor vehicles and industrial coal combustion. Conditional probability function (CPF analysis was applied to estimate the source locations using the PMF-resolved source contribution coupled with the surface wind direction data. Health exposure risk of hazardous trace elements (Pb, As, Si, Cr, Mn and Ni and source-specific values were estimated. The total hazard quotient (HQ of PM2.5 was 2.09, higher than the acceptable limit (HQ = 1. The total carcinogenic risk (CR was 3.37 × 10−3 for PM2.5, which was 3 times higher than the least stringent limit (1.0 × 10−4. Among the selected trace elements, As and Pb posed the highest non-carcinogenic and carcinogenic risks to human health, respectively. In addition, our results show that the industrial coal combustion source is the dominant non-carcinogenic and carcinogenic risk contributor, highlighting the need for stringent control of this source. This study provides new insight for policy makers to prioritize sources in air quality management and health risk reduction.

Comparative multielement analyses of airborne particulate samples collected in various areas

International Nuclear Information System (INIS)

Mamuro, Tetsuo; Matsuda, Yatsuka; Mizohata, Akira

1973-01-01

In order to grasp the characteristic features of the air pollution by particulates in various areas in Japan, multielement analyses by instrumental neutron activation analysis and radioisotope energy dispersive X-ray fluorescence analysis were applied to 31 airborne particulate samples collected in 15 different areas, and the analytical results obtained were compared with one another. All the samples were collected by so-called ''10 micron cut'' samplers, the collection efficiency of which is considered to be 50% at 8μ and nearly zero beyond 10μ. Among the areas in question there are clean seaside areas, heavily industrialized areas, small cities along the Inland Sea or the Pacific Ocean around which industrialization is progressing, a small city having only a big iron work, an area famous for its ceramic industry and so on. The atmospheres over them were found to be quite different not only in pollution extent but also in pollution pattern. (auth.)

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

Energy Technology Data Exchange (ETDEWEB)

Machado, C. M. [Federal Univ. of Amazonas (Brazil); Santos, Erickson O. [Federal Univ. of Amazonas (Brazil); Fernandes, Karenn S. [Federal Univ. of Amazonas (Brazil); Neto, J. L. [Federal Univ. of Amazonas (Brazil); Souza, Rodrigo A. [Univ. of the State of Amazonas (Brazil)

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.

Characteristics and source appointment of atmospheric particulate mercury over East China Sea: Implication on the deposition of atmospheric particulate mercury in marine environment.

Science.gov (United States)

Duan, Lian; Cheng, Na; Xiu, Guangli; Wang, Fujiang; Chen, Ying

2017-05-01

Total Suspended Particulate (TSP) samples were collected at Huaniao Island in northern East China Sea (ECS) from March 2012 to January 2013. Chemical analysis were conducted to measure the concentration of total particulate mercury (TPM) and speciated particulate mercury including HCl-soluble particulate mercury (HPM), elemental particulate mercury (EPM) and residual particulate mercury (RPM). The bromine (Br) and iodine (I) on particles were also detected. The mean concentration of TPM during the study period was 0.23 ± 0.15 ng m -3 , while the obviously seasonal variation was found that the concentrations of TPM in spring, summer, fall and winter were 0.34 ± 0.20 ng m -3 , 0.15 ± 0.03 ng m -3 , 0.15 ± 0.05 ng m -3 and 0.27 ± 0.26 ng m -3 , respectively. The statistically strong correlation of bromine and iodine to HPM was only found in spring with r = 0.81 and 0.77 (p mercury due to the deposition of mercury over the sea. The cluster of air mass across the sea had low concentration of HPM in winter, which suggested that the oxidation of mercury in winter might be related to other oxidants. During the whole sampling period, the air mass from the north of China contributed to the higher concentration of TPM in Huaniao Island. Copyright © 2016 Elsevier Ltd. All rights reserved.

Source apportionment of particulate pollutants in the atmosphere over the Northern Yellow Sea

Science.gov (United States)

Wang, L.; Qi, J. H.; Shi, J. H.; Chen, X. J.; Gao, H. W.

2013-05-01

Atmospheric aerosol samples were collected over the Northern Yellow Sea of China during the years of 2006 and 2007, in which the Total Carbon (TC), Cu, Pb, Cd, V, Zn, Fe, Al, Na+, Ca2+, Mg2+, NH4+, NO3-, SO42-, Cl-, and K+ were measured. The principle components analysis (PCA) and positive matrix factorization (PMF) receptor models were used to identify the sources of particulate matter. The results indicated that seven factors contributed to the atmospheric particles over the Northern Yellow Sea, i.e., two secondary aerosols (sulfate and nitrate), soil dust, biomass burning, oil combustion, sea salt, and metal smelting. When the whole database was considered, secondary aerosol formation contributed the most to the atmospheric particle content, followed by soil dust. Secondary aerosols and soil dust consisted of 65.65% of the total mass of particulate matter. The results also suggested that the aerosols over the North Yellow Sea were heavily influenced by ship emission over the local sea area and by continental agricultural activities in the northern China, indicating by high loading of V in oil combustion and high loading of K+ in biomass burning. However, the contribution of each factor varied greatly over the different seasons. In spring and autumn, soil dust and biomass burning were the dominant factors. In summer, heavy oil combustion contributed the most among these factors. In winter, secondary aerosols were major sources. Backward trajectories analysis indicated the 66% of air mass in summer was from the ocean, while the air mass is mainly from the continent in other seasons.

Sampling technologies and air pollution control devices for gaseous and particulate arsenic: a review

International Nuclear Information System (INIS)

Helsen, Lieve

2005-01-01

Direct measurement of arsenic release requires a good sampling and analysis procedure in order to capture and detect the total amount of metals emitted. The literature is extensively reviewed in order to evaluate the efficiency of full field-scale and laboratory scale techniques for capturing particulate and gaseous emissions of arsenic from the thermo-chemical treatment of different sources of arsenic. Furthermore, trace arsenic concentrations in ambient air, national standard sampling methods and arsenic analysis methods are considered. Besides sampling techniques, the use of sorbents is also reviewed with respect to both approaches (1) to prevent the metals from exiting with the flue gas and (2) to react or combine with the metals in order to be collected in air pollution control systems. The most important conclusion is that submicron arsenic fumes are difficult to control in conventional air pollution control devices. Complete capture of the arsenic species requires a combination of particle control and vapour control devices. - Submicron arsenic fumes are difficult to control in conventional air pollution control devices

Quantifying the environmental impact of particulate deposition from dry unpaved roadways

Energy Technology Data Exchange (ETDEWEB)

Becker, D.L.

1979-01-01

Airborne dust is the air pollutant most frequently observed to exceed National Ambient Air Quality Standards in rural areas. This pollutant (also referred to as suspended particulates) may originate from point sources (e.g., large areas of bare soil or pollen-producing vegetation.) Most sources of atmospheric particulates, whether natural or anthropogenic, are difficult to quantify by means of a source strength (i.e., mass of particulates emitted per unit time). A numerical model was developed for calculating the source strength and quantifying the atmospheric transport and eposition of dust generated on unpaved roadways. This model satisfies the second-order differential equation for the diffusion process and also the equation of mass conservation. Input to the model includes meterological variables, surface roughness characteristics, and the size distribution and suspended particulate concentration of dust as sampled downwind of an unpaved roadway. By using predetermined tolerance levels of airborne concentrations or tolerance levels of deposition, maximum allowable vehicular traffic volume can be established. The model also may be used to estimate reduction in photosynthesis resulting from fugitive dust from point or line sources. The contribug ion to sedimentation in aquatic bodies, resulting from airborne particulates also may be assessed with this model.

Elemental Quantification and Source Identification of Airborne Particulate Matter in Pathumwan District

International Nuclear Information System (INIS)

Chueinta, Wanna; Bunprapob, Suphamattree

2003-10-01

Airborne particulate matter (APM) is apparently the biggest air pollution problem found in capital and other big cities. APM has the adverse impact on human health and also on the environment. PM 10 (particle with aerodynamic diameter le ss than 10 μm), in particularly, can cause the respiratory diseases since it can penetrate the respiratory system. Furthermore, PM 25 (particle with aerodynamic diameter less than 2.5 μm) is the major cause of visibility impairment. This paper reports the study of urban air pollution at Pathumwan District, a business area in Bangkok City center. Coarse and fine fractions of PM 10 (P M-2 .2 - 10 and PM 2.2 , respectively) were collected by a Gent stacked filter unit air sampler during January-December 2002. The filter samples were measured for mass and black carbon. Elemental concentrations were analyzed by instrumental neutron activation analysis. The results indicate the rather high level of PM 10 at the sampling site. The annual average of PM 10 is 56.6 μg/m 3 compared to the ambient air quality standard of 50 μg/m 3 . The obtained data of black carbon and elemental concentrations were used for investigation of pollution sources by applying a receptor model called Positive Matrix Factorization. It could identify that the main sources were most likely city dust, emissions from vehicle combustion, incineration and sea-salt

Effects of Source-Apportioned Coarse Particulate Matter (PM) on Allergic Responses in Mice

Science.gov (United States)

The Cleveland Multiple Air Pollutant Study (CMAPS) is one of the first comprehensive studies conducted to evaluate particulate matter (PM) over local and regional scales. Cleveland and the nearby Ohio River Valley impart significant regional sources of air pollution including coa...

Chemical and biological characterization of urban particulate matter

International Nuclear Information System (INIS)

Agurell, E.; Alsberg, T.; Assefaz-Redda, Y.

1990-11-01

Airborne particulate matter has been collected on glass fiber filter by high volume sampling in the Goeteborg urban area. The samples were, after extraction with respect to organic components, tested for biological effect in the Salmonella mutagenicity assay, affinity to the cytosol TCDD receptor and toxicity towards a mammalian cell system and analysed chemically for selected polycyclic aromatic compounds. A series of samples collected simultaneously at a street level location and a rooftop site showed that most parameters associated with the organic compounds adsorbed to airborne particulate matter has similar concentrations at the two levels. The differences observed for the mutagenic effect in different strains and conditions showed that the rooftop samples had a different composition compared to the street samples indicating that atmospheric transformations have occurred. Chemical fractionation of representative samples showed that the distribution of mutagenic activity among different fractions is dissimilar to the distribution obtained in the fractionation of both gasoline and diesel engine exhaust particles. Partial least squares regression analysis showed qualitatively that diesel exhaust is a major source of airborne particulate mutagenic activity and source apportionment with chemical mass balance and multilinear regression corroborated this quantitatively. The multilinear regression analysis gave the result that the airborne activity in Salmonella TA90-S9 originated to 54±4% from diesel exhaust and to 26±3% from gasoline exhaust. The contribution is more equal for the activity measured with TA98+S9. The usefulness of short-term bioassays as an addition to chemical analysis of airborne particulate matter depends on whether only polycylic aromatic hydrocarbons (PAH) are major carcinogens, as has been suggested in the literature, or whether also other polycyclic aromatic compound (PAC) are of importance. (au)

Source apportionment of fine (PM1.8) and ultrafine (PM0.1) airborne particulate matter during a severe winter pollution episode.

Science.gov (United States)

Kleeman, Michael J; Riddle, Sarah G; Robert, Michael A; Jakober, Chris A; Fine, Phillip M; Hays, Michael D; Schauer, James J; Hannigan, Michael P

2009-01-15

Size-resolved samples of airborne particulate matter (PM) collected during a severe winter pollution episode at three sites in the San Joaquin Valley of California were extracted with organic solvents and analyzed for detailed organic compounds using GC-MS. Six particle size fractions were characterized with diameter (Dp) < 1.8 microm; the smallest size fraction was 0.056 < Dp < 0.1 microm which accounts for the majority of the mass in the ultrafine (PM0.1) size range. Source profiles for ultrafine particles developed during previous studies were applied to the measurements at each sampling site to calculate source contributions to organic carbon (OC) and elemental carbon (EC) concentrations. Ultrafine EC concentrations ranged from 0.03 microg m(-3) during the daytime to 0.18 microg m(-3) during the nighttime. Gasoline fuel, diesel fuel, and lubricating oil combustion products accounted for the majority of the ultrafine EC concentrations, with relatively minor contributions from biomass combustion and meat cooking. Ultrafine OC concentrations ranged from 0.2 microg m(-3) during the daytime to 0.8 microg m(-3) during the nighttime. Wood combustion was found to be the largest source of ultrafine OC. Meat cooking was also identified as a significant potential source of PM0.1 mass but further study is required to verify the contributions from this source. Gasoline fuel, diesel fuel, and lubricating oil combustion products made minor contributions to PM0.1 OC mass. Total ultrafine particulate matter concentrations were dominated by contributions from wood combustion and meat cooking during the current study. Future inhalation exposure studies may wish to target these sources as potential causes of adverse health effects.

DIII-D dust particulate characterization (June 1998 Vent)

International Nuclear Information System (INIS)

Carmack, W.J.

1999-01-01

Dust is a key component of fusion power device accident source term. Understanding the amount of dust expected in fusion power devices and its physical and chemical characteristics is needed to verify assumptions currently used in safety analyses. An important part of this safety research and development work is to characterize dust from existing experimental tokamaks. In this report, the authors present the collection, data analysis methods used, and the characterization of dust particulate collected from various locations inside the General Atomics DIII-D vacuum vessel following the June 1998 vent. The collected particulate was analyzed at the Idaho National Engineering and Environmental Laboratory (INEEL). Two methods were used to collect particulate with the goal of preserving the particle size distribution and physical characteristics of the particulate. Choice of collection technique is important because the sampling method used can bias the particle size distribution collected. Vacuum collection on substrates and adhesion removal with metallurgical replicating tape were chosen as non-intrusive sampling methods. Seventeen samples were collected including plasma facing surfaces in lower, upper, and horizontal locations, surfaces behind floor tiles, surfaces behind divert or tiles, and surfaces behind ceiling tiles. The results of the analysis are presented

Receptor model-based source apportionment of particulate pollution in Hyderabad, India.

Science.gov (United States)

Guttikunda, Sarath K; Kopakka, Ramani V; Dasari, Prasad; Gertler, Alan W

2013-07-01

Air quality in Hyderabad, India, often exceeds the national ambient air quality standards, especially for particulate matter (PM), which, in 2010, averaged 82.2 ± 24.6, 96.2 ± 12.1, and 64.3 ± 21.2 μg/m(3) of PM10, at commercial, industrial, and residential monitoring stations, respectively, exceeding the national ambient standard of 60 μg/m(3). In 2005, following an ordinance passed by the Supreme Court of India, a source apportionment study was conducted to quantify source contributions to PM pollution in Hyderabad, using the chemical mass balance (version 8.2) receptor model for 180 ambient samples collected at three stations for PM10 and PM2.5 size fractions for three seasons. The receptor modeling results indicated that the PM10 pollution is dominated by the direct vehicular exhaust and road dust (more than 60%). PM2.5 with higher propensity to enter the human respiratory tracks, has mixed sources of vehicle exhaust, industrial coal combustion, garbage burning, and secondary PM. In order to improve the air quality in the city, these findings demonstrate the need to control emissions from all known sources and particularly focus on the low-hanging fruits like road dust and waste burning, while the technological and institutional advancements in the transport and industrial sectors are bound to enhance efficiencies. Andhra Pradesh Pollution Control Board utilized these results to prepare an air pollution control action plan for the city.

Distribution and sources of particulate organic matter in the Indian monsoonal estuaries during monsoon

Digital Repository Service at National Institute of Oceanography (India)

Sarma, V.V.S.S.; Krishna, M.S.; Prasad, V.R.; Kumar, B.S.K.; Naidu, S.A.; Rao, G.D.; Viswanadham, R.; Sridevi, T.; Kumar, P.P.; Reddy, N.P.C.

The distribution and sources of particulate organic carbon (POC) and nitrogen (PN) in 27 Indian estuaries were examined during the monsoon using the content and isotopic composition of carbon and nitrogen. Higher phytoplankton biomass was noticed...

Particulate Trace Element Cycling in a Diatom Bloom at Station ALOHA

Science.gov (United States)

Weisend, R.; Morton, P. L.; Landing, W. M.; Fitzsimmons, J. N.; Hayes, C. T.; Boyle, E. A.

2014-12-01

Phytoplankton in oligotrophic marine deserts depend on remote sources to supply trace nutrients. To examine these sources, marine particulate matter samples from the central North Pacific (Station ALOHA) were collected during the July-August 2012 HOE-DYLAN cruises and analyzed for a suite of trace (e.g., Fe, Mn) and major (e.g. Al, P) elements. Daily surface SPM samples were examined for evidence of atmospheric deposition and biological uptake, while five vertical profiles were examined for evidence of surface vertical export and subsurface horizontal transport from nearby sources (e.g., margin sediments, hydrothermal plumes). Maxima in surface particulate P (a biological tracer) corresponded with a diatom bloom, and surprisingly also coincided with maxima in particulate Al (typically a tracer for lithogenic inputs). The surface particulate Al distributions likely result from the adsorption of dissolved Al onto diatom silica frustules, not from atmospheric dust deposition. In addition, a subsurface maximum in particulate Al and P was observed four days later at 75m, possibly resulting from vertical export of the surface diatom bloom. The distributions of other bioactive trace elements (e.g. Cd, Co, Cu) will be presented in the context of the diatom bloom and other biological, chemical and physical features. A second, complementary poster is also being presented which examines the cycling of trace elements in lithogenic particles (Morton et al., "Trace Element Cycling in Lithogenic Particles at Station ALOHA").

Source strengths for indoor human activities that resuspend particulate matter.

Science.gov (United States)

Ferro, Andrea R; Kopperud, Royal J; Hildemann, Lynn M

2004-03-15

A mathematical model was applied to continuous indoor and outdoor particulate matter (PM) measurements to estimate source strengths for a variety of prescribed human activities that resuspend house dust in the home. Activities included folding blankets, folding clothes, dry dusting, making a bed, dancing on a rug, dancing on a wood floor, vacuuming, and walking around and sitting on upholstered furniture. Although most of the resuspended particle mass from these activities was larger than 5 microm in diameter, the resuspension of PM2.5 and PM5 was substantial, with source strengths ranging from 0.03 to 0.5 mg min(-1) for PM2.5 and from 0.1 to 1.4 mg min(-1) for PM5. Source strengths for PM > 5 microm could not be quantified due to instrument limitations. The source strengths were found to be a function of the number of persons performing the activity, the vigor of the activity, the type of activity, and the type of flooring.

Diagnostic Air Quality Model Evaluation of Source-Specific Primary and Secondary Fine Particulate Carbon

Science.gov (United States)

Ambient measurements of 78 source-specific tracers of primary and secondary carbonaceous fine particulate matter collected at four midwestern United States locations over a full year (March 2004–February 2005) provided an unprecedented opportunity to diagnostically evaluate...

Source apportionment of fine particulate matter in China in 2013 using a source-oriented chemical transport model.

Science.gov (United States)

Shi, Zhihao; Li, Jingyi; Huang, Lin; Wang, Peng; Wu, Li; Ying, Qi; Zhang, Hongliang; Lu, Li; Liu, Xuejun; Liao, Hong; Hu, Jianlin

2017-12-01

China has been suffering high levels of fine particulate matter (PM 2.5 ). Designing effective PM 2.5 control strategies requires information about the contributions of different sources. In this study, a source-oriented Community Multiscale Air Quality (CMAQ) model was applied to quantitatively estimate the contributions of different source sectors to PM 2.5 in China. Emissions of primary PM 2.5 and gas pollutants of SO 2 , NO x , and NH 3 , which are precursors of particulate sulfate, nitrate, and ammonium (SNA, major PM 2.5 components in China), from eight source categories (power plants, residential sources, industries, transportation, open burning, sea salt, windblown dust and agriculture) were separately tracked to determine their contributions to PM 2.5 in 2013. Industrial sector is the largest source of SNA in Beijing, Xi'an and Chongqing, followed by agriculture and power plants. Residential emissions are also important sources of SNA, especially in winter when severe pollution events often occur. Nationally, the contributions of different source sectors to annual total PM 2.5 from high to low are industries, residential sources, agriculture, power plants, transportation, windblown dust, open burning and sea salt. Provincially, residential sources and industries are the major anthropogenic sources of primary PM 2.5 , while industries, agriculture, power plants and transportation are important for SNA in most provinces. For total PM 2.5 , residential and industrial emissions are the top two sources, with a combined contribution of 40-50% in most provinces. The contributions of power plants and agriculture to total PM 2.5 are about 10%, respectively. Secondary organic aerosol accounts for about 10% of annual PM 2.5 in most provinces, with higher contributions in southern provinces such as Yunnan (26%), Hainan (25%) and Taiwan (21%). Windblown dust is an important source in western provinces such as Xizang (55% of total PM 2.5 ), Qinghai (74%), Xinjiang (59

Nepal Ambient Monitoring and Source Testing Experiment (NAMaSTE): Emissions of particulate matter from wood and dung cooking fires, brick kilns, generators, trash and crop residue burning

Science.gov (United States)

Stone, Elizabeth; Jayarathne, Thilina; Stockwell, Chelsea; Christian, Ted; Bhave, Prakash; Siva Praveen, Puppala; Panday, Arnico; Adhikari, Sagar; Maharjan, Rashmi; Goetz, Doug; DeCarlo, Peter; Saikawa, Eri; Yokelson, Robert

2016-04-01

The Nepal Ambient Monitoring and Source Testing Experiment (NAMASTE) field campaign targeted the in situ characterization of widespread and under-sampled combustion sources. In Kathmandu and the Terai, southern Nepal's flat plains, samples of fine particulate matter (PM2.5) were collected from wood and dung cooking fires (n = 22), generators (n = 2), groundwater pumps (n = 2), clamp kilns (n = 3), zig-zag kilns (n = 3), trash burning (n = 4), one heating fire, and one crop residue fire. Co-located measurements of carbon dioxide, carbon monoxide, and volatile organic compounds allowed for the application of the carbon mass balance approach to estimate emission factors for PM2.5, elemental carbon, organic carbon, and water-soluble inorganic ions. Organic matter was chemically speciated using gas chromatography - mass spectrometry for polycyclic aromatic hydrocarbons, sterols, n-alkanes, hopanes, steranes, and levoglucosan, which accounted for 2-8% of the measured organic carbon. These data were used to develop molecular-marker based profiles for use in source apportionment modeling. This study provides quantitative emission factors for particulate matter and its constituents for many important combustion sources in Nepal and South Asia.

Contributions to cities' ambient particulate matter (PM): A systematic review of local source contributions at global level

Science.gov (United States)

Karagulian, Federico; Belis, Claudio A.; Dora, Carlos Francisco C.; Prüss-Ustün, Annette M.; Bonjour, Sophie; Adair-Rohani, Heather; Amann, Markus

2015-11-01

For reducing health impacts from air pollution, it is important to know the sources contributing to human exposure. This study systematically reviewed and analysed available source apportionment studies on particulate matter (of diameter of 10 and 2.5 microns, PM10 and PM2.5) performed in cities to estimate typical shares of the sources of pollution by country and by region. A database with city source apportionment records, estimated with the use of receptor models, was also developed and available at the website of the World Health Organization. Systematic Scopus and Google searches were performed to retrieve city studies of source apportionment for particulate matter. Six source categories were defined. Country and regional averages of source apportionment were estimated based on city population weighting. A total of 419 source apportionment records from studies conducted in cities of 51 countries were used to calculate regional averages of sources of ambient particulate matter. Based on the available information, globally 25% of urban ambient air pollution from PM2.5 is contributed by traffic, 15% by industrial activities, 20% by domestic fuel burning, 22% from unspecified sources of human origin, and 18% from natural dust and salt. The available source apportionment records exhibit, however, important heterogeneities in assessed source categories and incompleteness in certain countries/regions. Traffic is one important contributor to ambient PM in cities. To reduce air pollution in cities and the substantial disease burden it causes, solutions to sustainably reduce ambient PM from traffic, industrial activities and biomass burning should urgently be sought. However, further efforts are required to improve data availability and evaluation, and possibly to combine with other types of information in view of increasing usefulness for policy making.

Source contributions of fine particulate matter during one winter haze episodes in Xi'an, China

Science.gov (United States)

Yang, X.; Wu, Q.

2017-12-01

Long-term exposure to high levels of fine particulate matter (PM2.5) is found to be associated with adverse effects on human health, ecological environment and climate change. Identification the major source regions of fine particulate matter are essential to proposing proper joint prevention and control strategies for heavy haze mitigation. In this work, the Comprehensive Air Quality Model with extensions (CAMx) together with the Particulate Source Apportionment Technology (PSAT) and the Weather Research and Forecast Model (WRF), have been applied to analyze the major source regions of PM2.5 in Xi'an during the heavy haze episodes in winter (29, December, 2016 - 5 January 2017), and the framework of the model system is shown in Fig. 1. Firstly, according to the model evaluation of the daily PM2.5 concentrations for the two months, the model has well performance, and the fraction of predictions within a factor of 2 of the observations (FAC2) is 84%, while the correlation coefficient (R) is 0.80 in Xi'an. By using the PSAT in CAMx model, a detailed source region contribution matrix is derived for all points within the Xi'an region and its six surrounding areas, and long-range regional transport. The results show that the local emission in Xi'an is the mainly sources at downtown area, which contributing 72.9% as shown in Fig.2, and the contribution rate of transportations between adjacent areas depends on wind direction. Meanwhile, three different suburban areas selected for detailed analysis in fine particles sources. Comparing to downtown area, the sources of suburban areas are more multiply, and the transportations make the contribution 40%-82%. In the suburban areas, regional inflows play an important role in the fine particles concentrations, indicating a strong need for regional joint emission control efforts. The results enhance the quantitative understanding of the PM2.5 source regions and provide a basis for policymaking to advance the control of pollution

Results of Self-Absorption Study on the Versapor 3000 Filters for Radioactive Particulate Air Sampling

International Nuclear Information System (INIS)

Barnett, J.M.

2008-01-01

Since the mid-1980s the Pacific Northwest National Laboratory (PNNL) has used a value of 0.85 as a correction factor for the self absorption of activity of particulate radioactive air samples. More recently, an effort was made to evaluate the current particulate radioactive air sample filters (Versapor(reg s ign) 3000) used at PNNL for self absorption effects. There were two methods used in the study, (1) to compare the radioactivity concentration by direct gas-flow proportional counting of the filter to the results obtained after acid digestion of the filter and counting again by gas-flow proportional detection and (2) to evaluate sample filters by high resolution visual/infrared microscopy to determine the depth of material loading on or in the filter fiber material. Sixty samples were selected from the archive for acid digestion in the first method and about 30 samples were selected for high resolution visual/infrared microscopy. Mass loading effects were also considered. From the sample filter analysis, large error is associated with the average self absorption factor, however, when the data is compared directly one-to-one, statistically, there appears to be good correlation between the two analytical methods. The mass loading of filters evaluated was <0.2 mg cm-2 and was also compared against other published results. The microscopy analysis shows the sample material remains on the top of the filter paper and does not imbed into the filter media. Results of the microscopy evaluation lead to the conclusion that there is not a mechanism for significant self absorption. The overall conclusion is that self-absorption is not a significant factor in the analysis of filters used at PNNL for radioactive air stack sampling of radionuclide particulates and that an applied correction factor is conservative in determining overall sample activity. A new self absorption factor of 1.0 is recommended

Mercury, trace elements and organic constituents in atmospheric fine particulate matter, Shenandoah National Park, Virginia, USA: A combined approach to sampling and analysis

Science.gov (United States)

Kolker, A.; Engle, M.A.; Orem, W.H.; Bunnell, J.E.; Lerch, H.E.; Krabbenhoft, D.P.; Olson, M.L.; McCord, J.D.

2008-01-01

Compliance with U.S. air quality regulatory standards for atmospheric fine particulate matter (PM2.5) is based on meeting average 24 hour (35 ?? m-3) and yearly (15 ??g m-3) mass-per-unit-volume limits, regardless of PM2.5 composition. Whereas this presents a workable regulatory framework, information on particle composition is needed to assess the fate and transport of PM2.5 and determine potential environmental/human health impacts. To address these important non-regulatory issues an integrated approach is generally used that includes (1) field sampling of atmospheric particulate matter on filter media, using a size-limiting cyclone, or with no particle-size limitation; and (2) chemical extraction of exposed filters and analysis of separate particulate-bound fractions for total mercury, trace elements and organic constituents, utilising different USGS laboratories optimised for quantitative analysis of these substances. This combination of sampling and analysis allowed for a more detailed interpretation of PM2.5 sources and potential effects, compared to measurements of PM2.5 abundance alone. Results obtained using this combined approach are presented for a 2006 air sampling campaign in Shenandoah National Park (Virginia, USA) to assess sources of atmospheric contaminants and their potential impact on air quality in the Park. PM2.5 was collected at two sampling sites (Big Meadows and Pinnacles) separated by 13.6 km. At both sites, element concentrations in PM2.5 were low, consistent with remote or rural locations. However, element/Zr crustal abundance enrichment factors greater than 10, indicating anthropogenic input, were found for Hg, Se, S, Sb, Cd, Pb, Mo, Zn and Cu, listed in decreasing order of enrichment. Principal component analysis showed that four element associations accounted for 84% of the PM 2.5 trace element variation; these associations are interpreted to represent: (1) crustal sources (Al, REE); (2) coal combustion (Se, Sb), (3) metal production

Size distribution and source identification of total suspended particulate matter and associated heavy metals in the urban atmosphere of Delhi.

Science.gov (United States)

Srivastava, Arun; Jain, V K

2007-06-01

A study of the atmospheric particulate size distribution of total suspended particulate matter (TSPM) and associated heavy metal concentrations has been carried out for the city of Delhi. Urban particles were collected using a five-stage impactor at six sites in three different seasons, viz. winter, summer and monsoon in the year 2001. Five samples from each site in each season were collected. Each sample (filter paper) was extracted with a mixture of nitric acid, hydrochloric acid and hydrofluoric acid. The acid solutions of the samples were analysed in five-particle fractions by atomic absorption spectrometry (AAS). The impactor stage fractionation of particles shows that a major portion of TSPM concentration is in the form of PM0.7 (i.e. metal mass viz. Mn, Cr, Cd, Pb, Ni, and Fe are also concentrated in the PM0.7 mode. The only exceptions are size distributions pertaining to Cu and Ca. Though, Cu is more in PM0.7 mode, its presence in size intervals 5.4-1.6microm and 1.6-0.7microm is also significant, whilst in case of Ca there is no definite pattern in its distribution with size of particles. The average PM10.9 (i.e. Source apportionment reveals that there are two sources of TSPM and PM10.9, while three and four sources were observed for PM1.6 (i.e. <1.6microm) and PM0.7, respectively. Results of regression analyses show definite correlations between PM10.9 and other fine size fractions, suggesting PM10.9 may adequately act as a surrogate for both PM1.6 and PM0.7, while PM1.6 may adequately act as a surrogate for PM0.7.

SOURCE SAMPLING FINE PARTICULATE MATTER--INSTITUTIONAL OIL-FIRED BOILER

Science.gov (United States)

EPA seeks to understand the correlation between ambient fine PM and adverse human health effects, and there are no reliable emission factors to use for estimating PM2.5 or NH3. The most common source of directly emitted PM2.5 is incomplete combustion of fossil or biomass fuels. M...

Laser ablation-inductively coupled plasma-mass spectrometry: Examinations of the origins of polyatomic ions and advances in the sampling of particulates

Energy Technology Data Exchange (ETDEWEB)

Witte, Travis [Iowa State Univ., Ames, IA (United States)

2011-01-01

This dissertation provides a general introduction to Inductively coupled plasma-mass spectrometry (ICP-MS) and laser ablation (LA) sampling, with an examination of analytical challenges in the employment of this technique. It discusses the origin of metal oxide ions (MO+) in LA-ICP-MS, as well as the effect of introducing helium and nitrogen to the aerosol gas flow on the formation of these polyatomic interferences. It extends the study of polyatomic ions in LA-ICP-MS to metal argide (MAr+) species, an additional source of possible significant interferences in the spectrum. It describes the application of fs-LA-ICP-MS to the determination of uranium isotope ratios in particulate samples.

Sampling and analytical methodologies for instrumental neutron activation analysis of airborne particulate matter

International Nuclear Information System (INIS)

1992-01-01

The IAEA supports a number of projects having to do with the analysis of airborne particulate matter by nuclear techniques. Most of this work involves the use of activation analysis in its various forms, particularly instrumental neutron activation analysis (INAA). This technique has been widely used in many different countries for the analysis of airborne particulate matter, and there are already many publications in scientific journals, books and reports describing such work. The present document represents an attempt to summarize the most important features of INAA as applied to the analysis of airborne particulate matter. It is intended to serve as a set of guidelines for use by participants in the IAEA's own programmes, and other scientists, who are not yet fully experienced in the application of INAA to airborne particulate samples, and who wish either to make a start on using this technique or to improve their existing procedures. The methodologies for sampling described in this document are of rather general applicability, although they are presented here in a way that takes account of the particular requirements arising from the use of INAA as the analytical technique. The analytical part of the document, however, is presented in a form that is applicable only to INAA. (Subsequent publications in this series are expected to deal specifically with other nuclear related techniques such as energy dispersive X ray fluorescence (ED-XRF) and particle induced X ray emission (PIXE) analysis). Although the methods and procedures described here have been found through experience to yield acceptable results, they should not be considered mandatory. Any other procedure used should, however, be chosen to be capable of yielding results at least of equal quality to those described

Sampling and analytical methodologies for instrumental neutron activation analysis of airborne particulate matter

Energy Technology Data Exchange (ETDEWEB)

NONE

1992-12-01

The IAEA supports a number of projects having to do with the analysis of airborne particulate matter by nuclear techniques. Most of this work involves the use of activation analysis in its various forms, particularly instrumental neutron activation analysis (INAA). This technique has been widely used in many different countries for the analysis of airborne particulate matter, and there are already many publications in scientific journals, books and reports describing such work. The present document represents an attempt to summarize the most important features of INAA as applied to the analysis of airborne particulate matter. It is intended to serve as a set of guidelines for use by participants in the IAEA's own programmes, and other scientists, who are not yet fully experienced in the application of INAA to airborne particulate samples, and who wish either to make a start on using this technique or to improve their existing procedures. The methodologies for sampling described in this document are of rather general applicability, although they are presented here in a way that takes account of the particular requirements arising from the use of INAA as the analytical technique. The analytical part of the document, however, is presented in a form that is applicable only to INAA. (Subsequent publications in this series are expected to deal specifically with other nuclear related techniques such as energy dispersive X ray fluorescence (ED-XRF) and particle induced X ray emission (PIXE) analysis). Although the methods and procedures described here have been found through experience to yield acceptable results, they should not be considered mandatory. Any other procedure used should, however, be chosen to be capable of yielding results at least of equal quality to those described.

Local and regional sources of fine and coarse particulate matter based on traffic and background monitoring

Science.gov (United States)

Dimitriou, Konstantinos; Kassomenos, Pavlos

2014-05-01

The aim of this study was to identify local and exogenous sources affecting particulate matter (PM) levels in five major cities of Northern Europe namely: London, Paris, Hamburg, Copenhagen and Stockholm. Besides local emissions, PM profile at urban and suburban areas of the European Union (EU) is also influenced by regional PM sources due to atmospheric transport, thus geographical city distribution is of a great importance. At each city, PM10, PM2.5, NO2, SO2, CO and O3 air pollution data from two air pollution monitoring stations of the EU network were used. Different background characteristics of the selected two sampling sites at each city facilitated comparisons, providing a more exact analysis of PM sources. Four source apportionment methods: Pearson correlations among the levels of particulates and gaseous pollutants, characterisation of primal component analysis components, long-range transport analysis and extrapolation of PM size distribution ratios were applied. In general, fine (PM2.5) and coarse (PM10) particles were highly correlated, thus common sources are suggested. Combustion-originated gaseous pollutants (CO, NO2, SO2) were strongly associated to PM10 and PM2.5, primarily at areas severely affected by traffic. On the contrary, at background stations neighbouring important natural sources of particles or situated in suburban areas with rural background, natural emissions of aerosols were indicated. Series of daily PM2.5/PM10 ratios showed that minimum fraction values were detected during warm periods, due to higher volumes of airborne biogenic PM coarse, mainly at stations with important natural sources of particles in their vicinity. Hybrid single-particle Lagrangian integrated trajectory model was used, in order to extract 4-day backward air mass trajectories that arrived in the five cities which are under study during days with recorded PM10 exceedances. At all five cities, a significantly large fraction of those trajectories were classified

Source apportionment of the particulate PAHs at Seoul, Korea: impact of long range transport to a megacity

Directory of Open Access Journals (Sweden)

J. Y. Lee

2007-07-01

Full Text Available Northeast Asia including China, Korea, and Japan is one of the world's largest fossil fuel consumption regions. Seoul, Korea, is a megacity in Northeast Asia. Its emissions of air pollutants can affect the region, and in turn it is also affected by regional emissions. To understand the extent of these influences, major sources of ambient particulate PAHs in Seoul were identified and quantified based on measurements made between August 2002 and December 2003. The chemical mass balance (CMB model was applied. Seven major emission sources were identified based on the emission data in Seoul and Northeast Asia: Gasoline and diesel vehicles, residential coal use, coke ovens, coal power plants, biomass burning, and natural gas (NG combustion. The major sources of particulate PAHs in Seoul during the whole measurement period were gasoline and diesel vehicles, together accounted for 31% of the measured particulate PAHs levels. However, the source contributions showed distinct daily and seasonal variations. High contributions of biomass burning and coal (residential and coke oven were observed in fall and winter, accounting for 63% and 82% of the total concentration of PAHs, respectively. Since these sources were not strong in and around Seoul, they are likely to be related to transport from outside of Seoul, from China and/or North Korea. This implies that the air quality in a mega-city such as Seoul can be influenced by the long range transport of air pollutants such as PAHs.

Properties and cellular effects of particulate matter from direct emissions and ambient sources.

Science.gov (United States)

Jin, Wenjie; Su, Shu; Wang, Bin; Zhu, Xi; Chen, Yilin; Shen, Guofeng; Liu, Junfeng; Cheng, Hefa; Wang, Xilong; Wu, Shuiping; Zeng, Eddy; Xing, Baoshan; Tao, Shu

2016-10-14

The pollution of particulate matter (PM) is of great concern in China and many other developing countries. It is generally recognized that the toxicity of PM is source and property dependent. However, the relationship between PM properties and toxicity is still not well understood. In this study, PM samples from direct emissions of wood, straw, coal, diesel combustion, cigarette smoking and ambient air were collected and characterized for their physicochemical properties. Their expression of intracellular reactive oxygen species (ROS) and levels of inflammatory cytokines (i.e., tumor necrosis factor-α (TNF-α)) was measured using a RAW264.7 cell model. Our results demonstrated that the properties of the samples from different origins exhibited remarkable differences. Significant increases in ROS were observed when the cells were exposed to PMs from biomass origins, including wood, straw and cigarettes, while increases in TNF-α were found for all the samples, particularly those from ambient air. The most important factor associated with ROS generation was the presence of water-soluble organic carbon, which was extremely abundant in the samples that directly resulted from biomass combustion. Metals, endotoxins and PM size were the most important properties associated with increases in TNF-α expression levels. The association of the origins of PM particles and physicochemical properties with cytotoxic properties is illustrated using a cluster analysis.

Source identification of particulate matter in a semi-urban area of Malaysia using multivariate techniques.

Science.gov (United States)

Wahid, N B A; Latif, M T; Suan, L S; Dominick, D; Sahani, M; Jaafar, S A; Mohd Tahir, N

2014-03-01

This study aims to determine the composition and sources of particulate matter with an aerodynamic diameter of 10 μm or less (PM10) in a semi-urban area. PM10 samples were collected using a high volume sampler. Heavy metals (Fe, Zn, Pb, Mn, Cu, Cd and Ni) and cations (Na(+), K(+), Ca(2+) and Mg(2+)) were detected using inductively coupled plasma mass spectrometry, while anions (SO4 (2-), NO3 (-), Cl(-) and F(-)) were analysed using Ion Chromatography. Principle component analysis and multiple linear regressions were used to identify the source apportionment of PM10. Results showed the average concentration of PM10 was 29.5 ± 5.1 μg/m(3). The heavy metals found were dominated by Fe, followed by Zn, Pb, Cu, Mn, Cd and Ni. Na(+) was the dominant cation, followed by Ca(2+), K(+) and Mg(2+), whereas SO4 (2-) was the dominant anion, followed by NO3 (-), Cl(-) and F(-). The main sources of PM10 were the Earth's crust/road dust, followed by vehicle emissions, industrial emissions/road activity, and construction/biomass burning.

Aged riverine particulate organic carbon in four UK catchments

International Nuclear Information System (INIS)

Adams, Jessica L.; Tipping, Edward; Bryant, Charlotte L.; Helliwell, Rachel C.; Toberman, Hannah; Quinton, John

2015-01-01

The riverine transport of particulate organic matter (POM) is a significant flux in the carbon cycle, and affects macronutrients and contaminants. We used radiocarbon to characterise POM at 9 riverine sites of four UK catchments (Avon, Conwy, Dee, Ribble) over a one-year period. High-discharge samples were collected on three or four occasions at each site. Suspended particulate matter (SPM) was obtained by centrifugation, and the samples were analysed for carbon isotopes. Concentrations of SPM and SPM organic carbon (OC) contents were also determined, and were found to have a significant negative correlation. For the 7 rivers draining predominantly rural catchments, PO 14 C values, expressed as percent modern carbon absolute (pMC), varied little among samplings at each site, and there was no significant difference in the average values among the sites. The overall average PO 14 C value for the 7 sites of 91.2 pMC corresponded to an average age of 680 14 C years, but this value arises from the mixing of differently-aged components, and therefore significant amounts of organic matter older than the average value are present in the samples. Although topsoil erosion is probably the major source of the riverine POM, the average PO 14 C value is appreciably lower than topsoil values (which are typically 100 pMC). This is most likely explained by inputs of older subsoil OC from bank erosion, or the preferential loss of high- 14 C topsoil organic matter by mineralisation during riverine transport. The significantly lower average PO 14 C of samples from the River Calder (76.6 pMC), can be ascribed to components containing little or no radiocarbon, derived either from industrial sources or historical coal mining, and this effect is also seen in the River Ribble, downstream of its confluence with the Calder. At the global scale, the results significantly expand available information for PO 14 C in rivers draining catchments with low erosion rates. - Highlights: �

Characteristics of fine particulate matter and its sources in an industrialized coastal city, Ningbo, Yangtze River Delta, China

Science.gov (United States)

Wang, Weifeng; Yu, Jie; Cui, Yang; He, Jun; Xue, Peng; Cao, Wan; Ying, Hongmei; Gao, Wenkang; Yan, Yingchao; Hu, Bo; Xin, Jinyuan; Wang, Lili; Liu, Zirui; Sun, Yang; Ji, Dongsheng; Wang, Yuesi

2018-05-01

Chemical information is essential in understanding the characteristics of airborne particles, and effectively controlling airborne particulate matter pollution, but it remains unclear in some regions due to the scarcity of measurement data. In the present study, 92 daily PM2.5 (particulate matter with an aerodynamic diameter ≤ 2.5 μm) samples as well as historical observation data of air pollutants were collected in urban Ningbo, one of important industrial cities in the coastal area of the Yangtze River Delta, China in autumn and winter (from Nov. 2014 to Feb. 2015). Various chemical species in PM2.5 were determined including water soluble ions, organic and elemental carbon and elements. Positive matrix factorization model, cluster analysis of back trajectories, potential source contribution function (PSCF) model and concentration-weighted trajectory (CWT) model were used for identifying sources, apportioning contributions from each source and tracking potential areas of sources. The results showed the PM2.5 concentration has been reducing; nonetheless, the concentrations of PM2.5 are still much higher than the World Health Organization guideline with high PM2.5 concentrations observed in autumn and winter for the past few years. During the sampling period, the average PM2.5 mass concentration was 77 μg/m3 with the major components of OC, NO3-, SO42 -, NH4+ and EC, accounting for 24.7, 18.8, 14.5, 11.8 and 6.4% in the total mass concentration, respectively. When the aerosol pollution got worse during the sampling period, the NO3-, SO42 - and NH4+ concentrations increased accordingly and NO3- appeared to increase at fastest rate. SO42 - transported from industrial areas led to slight difference in spatial distribution of SO42 - in Ningbo. More secondary organic carbon was formed and the enrichment factor values of Cu, Ag, Cd, Sn and Pb increased with the degradation of air quality. Ten types of sources were identified for PM2.5 in the autumn and winter of

Particulate matter and neutron activation analysis

International Nuclear Information System (INIS)

Otoshi, Tsunehiko

2003-01-01

In these years, economy of East Asian region is rapidly growing, and countries in this region are facing serious environmental problems. Neutron activation analysis is known as one of high-sensitive analytical method for multi elements. And it is a useful tool for environmental research, particularly for the study on atmospheric particulate matter that consists of various constituents. Elemental concentration represents status of air, such as emission of heavy metals from industries and municipal incinerators, transportation of soil derived elements more than thousands of kilometers, and so on. These monitoring data obtained by neutron activation analysis can be a cue to evaluate environment problems. Japanese government launched National Air Surveillance Network (NASN) employing neutron activation analysis in 1974, and the data has been accumulated at about twenty sampling sites. As a result of mitigation measure of air pollution sources, concentrations of elements that have anthropogenic sources decreased particularly at the beginning of the monitoring period. However, even now, concentrations of these anthropogenic elements reflect the characteristics of each sampling site, e.g. industrial/urban, rural, and remote. Soil derived elements have a seasonal variation because of the contribution of continental dust transported by strong westerly winds prevailing in winter and spring season. The health effects associated with trace elements in particulate matter have not been well characterized. However, there is increasing evidence that particulate air pollution, especially fine portion of particles in many different cities is associated with acute mortality. Neutron activation analysis is also expected to provide useful information to this new study field related to human exposures and health risk. (author)

Composition and oxidation state of sulfur in atmospheric particulate matter

Directory of Open Access Journals (Sweden)

A. F. Longo

2016-10-01

Full Text Available 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.

CHARACTERISTIC OF AIRBORNE PARTICULATE MATTER SAMPLES COLLECTED FROM TWO SEMI INDUSTRIAL SITES IN BANDUNG, INDONESIA

Directory of Open Access Journals (Sweden)

Diah Dwiana Lestiani

2013-12-01

Full Text Available Air particulate matter concentrations, black carbon as well as elemental concentrations in two semi industrial sites were investigated as a preliminary study for evaluation of air quality in these areas. Sampling of airborne particulate matter was conducted in July 2009 using a Gent stacked filter unit sampler and a total of 18 pairs of samples were collected. Black carbon was determined by reflectance measurement and elemental analysis was performed using particle induced X-ray emission (PIXE. Elements Na, Mg, Al, Si, P, S, Cl, K, Ca, Ti, Cr, Mn, Fe, Cu, Zn and As were detected. Twenty four hour PM2.5 concentration at semi industrial sites Kiaracondong and Holis ranged from 4.0 to 22.2 µg m-3, while the PM10 concentration ranged from 24.5 to 77.1 µg m-3. High concentration of crustal elements, sulphur and zinc were identified in fine and coarse fractions for both sites. The fine fraction data from both sites were analyzed using a multivariate principal component analysis and for Kiaracondong site, identified factors are attributed to sea-salt with soil dust, vehicular emissions and biomass burning, non ferrous smelter, and iron/steel work industry, while for Holis site identified factors are attributed to soil dust, industrial emissions, vehicular emissions with biomass burning, and sea-salt. Although particulate samples were collected from semi industrial sites, vehicular emissions constituted with S, Zn and BC were identified in both sites.

Characterizing Aggregated Exposure to Primary Particulate Matter: Recommended Intake Fractions for Indoor and Outdoor Sources

DEFF Research Database (Denmark)

Fantke, Peter; Jolliet, Olivier; Apte, Joshua Schulz

2017-01-01

Exposure to fine particulate matter (PM_(2.5)) from indoor and outdoor sources is a leading environmental contributor to global disease burden. In response, we established under the auspices of the UNEP/SETAC Life Cycle Initiative a coupled indoor-outdoor emission-to-exposure framework to provide...

Source contributions and regional transport of primary particulate matter in China.

Science.gov (United States)

Hu, Jianlin; Wu, Li; Zheng, Bo; Zhang, Qiang; He, Kebin; Chang, Qing; Li, Xinghua; Yang, Fumo; Ying, Qi; Zhang, Hongliang

2015-12-01

A source-oriented CMAQ was applied to determine source sector/region contributions to primary particulate matter (PPM) in China. Four months were simulated with emissions grouped to eight regions and six sectors. Predicted elemental carbon (EC), primary organic carbon (POC), and PPM concentrations and source contributions agree with measurements and have significant spatiotemporal variations. Residential is a major contributor to spring/winter EC (50-80%), POC (60%-90%), and PPM (30-70%). For summer/fall, industrial contributes 30-50% for EC/POC and 40-60% for PPM. Transportation is more important for EC (20-30%) than POC/PPM (Guangzhou and Chongqing. Dust contributes to 1/3-1/2 in spring/fall of Beijing, Xi'an and Chongqing. Based on sector-region combination, local residential/transportation and residential/industrial from Heibei are major contributors to spring PPM in Beijing. In summer/fall, local industrial is the largest. In winter, residential/industrial from local and Hebei account for >90% in Beijing. Copyright © 2015 Elsevier Ltd. All rights reserved.

IDENTIFICATION OF POSSIBLE SOURCES OF PARTICULATE MATTER IN THE PERSONAL CLOUD USING SEM/EDX

Science.gov (United States)

The United States Environmental Protection Agency (U.S. EPA) conducted the Baltimore Particulate Matter (PM) Epidemiology-Exposure Study of the Elderly during the summer of 1998. The study design included PM2.5 samples obtained from elderly (65+ years of age) retirement facility ...

Source identification and long-term monitoring of airborne particulate matter (PM2.5/PM10) in an urban region of Korea

International Nuclear Information System (INIS)

Yong-Sam Chung; Sun-Ha Kim; Jong-Hwa Moon; Young-Jin Kim; Jong-Myoung Lim; Jin-Hong Lee

2006-01-01

For the identification of air pollution sources, about 500 airborne particulate matter (PM 2.5 and PM 10 ) samples were collected by using a Gent air sampler and a polycarbonate filter in an urban region in the middle of Korea from 2000 to 2003. The concentrations of 25 elements in the samples were measured by using instrumental neutron activation analysis (INAA). Receptor modeling was performed on the air monitoring data by using the positive matrix factorization (PMF2) method. According to this analysis, the existence of 6 to 10 PMF factors, such as metal-alloy, oil combustion, diesel exhaust, coal combustion, gasoline exhaust, incinerator, Cu-smelter, biomass burning, sea-salt, and soil dust were identified. (author)

Source identification and metallic profiles of size-segregated particulate matters at various sites in Delhi.

Science.gov (United States)

Hazarika, Naba; Jain, V K; Srivastava, Arun

2015-09-01

A study of elemental composition in the ambient air of Delhi was carried out in the monsoon, winter and summer seasons at four different sites from August 2012 to April 2013 in the size ranges 10 μm using "Dekati PM10" impactor. At each site, three samples were collected and were analyzed by energy-dispersive X-ray fluorescence (EDXRF). The presence of elements was found to be very common and highly concentrated in aerosol particles at all the sites, which are Na, Al, Si, K, Ca, Zn and Ba. Total suspended particulate matters (TSPMs) of fine particles were found high in comparison to coarse particles at all seasons. The TSPM of fine particles was found to be varied in the range from 303.6 to 416.2 μg/m(3). Similarly, the range of coarse TSPM was observed from 162.9 to 262.8 μg/m(3). Correlation matrices were observed between fine (size ranges 10 μm) size particles for all elements with seasons. Source apportionments of elements were carried out using MS Excel 2010 through XLSTAT software. The source apportionments between fine and coarse particles were carried out through factor analysis and dominated sources found to be crustal re-suspension and industrial activities.

[Distribution and source of particulate organic carbon and particulate nitrogen in the Yangtze River Estuary in summer 2012].

Science.gov (United States)

Xing, Jian-Wei; Xian, Wei-Wei; Sheng, Xiu-Zhen

2014-07-01

Based on the data from the cruise carried out in August 2012 in the Yangtze River Estuary and its adjacent waters, spatial distributions of particulate organic carbon (POC), particulate nitrogen (PN) and their relationships with environmental factors were studied, and the source of POC and the contribution of phytoplankton to POC were analyzed combined with n (C)/n (N) ratio and chlorophyll a (Chl a) in the Yangtze River Estuary in summer 2012. The results showed that the concentrations of POC in the Yangtze River Estuary ranged from 0.68 mg x L(-1) to 34.80 mg x L(-1) in summer and the average content was 3.74 mg x L(-1), and PN contents varied between 0.03 mg x L(-1) and 9.13 mg x L(-1) with an average value of 0.57 mg x L(-1). Both of them presented that the concentrations in bottom layers were higher than those in the surface. POC and PN as well as total suspended matter (TSM) showed a extremel similar horizontal distribution trend that the highest values appeared in the near of the mouth and southwest of the survey waters, and decreased rapidly as toward the open seas, both of them showed higher contents in coastal zones and lower in outer sea. There was a fairly good positive linear relationship between POC and PN, which indicated that they had the same source. POC and PN expressed significantly positive correlations with TSM and chemical oxygen demand (COD), but showed relatively weak correlations with salinit and chlorophyll a, which demonstrated that terrestrial inputs had a strong influence on the distribution of POC and PN, and phytoplankton production was not the major source of organic matters in the Yangtze River Estuary. Both the n (C)/n (N) ratio and POC/Chl a analysis showed that the main source of POC was terrestrial inputs, and organic debris was the main existence form of POC. Quantitative analysis showed the biomass of phytoplankton only made an average of 2.54% contribution to POC in the Yangtze Rive Estuary in summer and non-living POC

Spatial and temporal variation of sources contributing to quasi-ultrafine particulate matter PM0.36 in Augsburg, Germany.

Science.gov (United States)

Li, Fengxia; Schnelle-Kreis, Jürgen; Cyrys, Josef; Wolf, Kathrin; Karg, Erwin; Gu, Jianwei; Orasche, Jürgen; Abbaszade, Gülcin; Peters, Annette; Zimmermann, Ralf

2018-08-01

to study the sources contributing to quasi-ultrafine particle (UFP) organic carbon and the spatial temporal variability of the sources. 24h quasi-UFP (particulate matter quasi-UFP vary among sites and source types and show source-specific characteristics. Therefore, caution should be taken when using one monitor site measurement to assess human exposure in health effect studies of quasi-UFP. Copyright © 2018 Elsevier B.V. All rights reserved.

Atmospheric particulate mercury at the urban and forest sites in central Poland.

Science.gov (United States)

Siudek, Patrycja; Frankowski, Marcin; Siepak, Jerzy

2016-02-01

Particulate mercury concentrations were investigated during intensive field campaigns at the urban and forest sites in central Poland, between April 2013 and October 2014. For the first time, quantitative determination of total particulate mercury in coarse (PHg2.2) and fine (PHg0.7) aerosol samples was conducted in Poznań and Jeziory. The concentrations in urban fine and coarse aerosol fractions amounted to mercury concentrations. A strong impact of meteorological conditions (wind velocity, air mass direction, air temperature, and precipitation amount) on particulate mercury concentrations was also observed. In particular, higher variation and concentration range of PHg0.7 and PHg2.2 was reported for wintertime measurements. An increase in atmospheric particulate mercury during the cold season in the study region indicated that coal combustion, i.e., residential and industrial heating, is the main contribution factor for the selected particle size modes. Coarse particulate Hg at the urban site during summer was mainly attributed to anthropogenic sources, with significant contribution from resuspension processes and long-range transport. The highest values of PHg0.7 and PHg2.2 were found during westerly and southerly wind events, reflecting local emission from highly polluted areas. The period from late fall to spring showed that advection from the southern part of Poland was the main factor responsible for elevated Hg concentrations in fine and coarse particles in the investigated region. Moreover, September 2013 could be given as an example of the influence of additional urban activities which occurred approx. 10 m from the sampling site-construction works connected with replacement of the road surface, asphalting, etc. The concentrations of particulate Hg (>600.0 pg m(-3)) were much higher than during the following months when any similar situation did not occur. Our investigations confirmed that Hg in urban aerosol samples was predominantly related to local

Demonstration of Novel Sampling Techniques for Measurement of Turbine Engine Volatile and Non-Volatile Particulate Matter (PM) Emissions

Science.gov (United States)

2017-03-06

WP-201317) Demonstration of Novel Sampling Techniques for Measurement of Turbine Engine Volatile and Non-volatile Particulate Matter (PM... Engine Volatile and Non-Volatile Particulate Matter (PM) Emissions 6. AUTHOR(S) E. Corporan, M. DeWitt, C. Klingshirn, M.D. Cheng, R. Miake-Lye, J. Peck...the performance and viability of two devices to condition aircraft turbine engine exhaust to allow the accurate measurement of total (volatile and non

Aged riverine particulate organic carbon in four UK catchments

Energy Technology Data Exchange (ETDEWEB)

Adams, Jessica L., E-mail: jesams@ceh.ac.uk [Centre for Ecology and Hydrology, Lancaster Environment Centre, Lancaster, LA1 4AP (United Kingdom); Tipping, Edward, E-mail: et@ceh.ac.uk [Centre for Ecology and Hydrology, Lancaster Environment Centre, Lancaster, LA1 4AP (United Kingdom); Bryant, Charlotte L., E-mail: charlotte.bryant@glasgow.ac.uk [NERC Radiocarbon Facility, East Kilbride G75 0QF, Scotland (United Kingdom); Helliwell, Rachel C., E-mail: rachel.helliwell@hutton.ac.uk [The James Hutton Institute, Craigiebuckler, Aberdeen AB15 8QH Scotland (United Kingdom); Toberman, Hannah, E-mail: hannahtoberman@hotmail.com [Centre for Ecology and Hydrology, Lancaster Environment Centre, Lancaster, LA1 4AP (United Kingdom); School of Environmental Sciences, University of Liverpool, Liverpool L69 3GP (United Kingdom); Quinton, John, E-mail: j.quinton@lancaster.ac.uk [Lancaster Environment Centre, Lancaster University, Lancaster LA1 4YQ (United Kingdom)

2015-12-01

The riverine transport of particulate organic matter (POM) is a significant flux in the carbon cycle, and affects macronutrients and contaminants. We used radiocarbon to characterise POM at 9 riverine sites of four UK catchments (Avon, Conwy, Dee, Ribble) over a one-year period. High-discharge samples were collected on three or four occasions at each site. Suspended particulate matter (SPM) was obtained by centrifugation, and the samples were analysed for carbon isotopes. Concentrations of SPM and SPM organic carbon (OC) contents were also determined, and were found to have a significant negative correlation. For the 7 rivers draining predominantly rural catchments, PO{sup 14}C values, expressed as percent modern carbon absolute (pMC), varied little among samplings at each site, and there was no significant difference in the average values among the sites. The overall average PO{sup 14}C value for the 7 sites of 91.2 pMC corresponded to an average age of 680 {sup 14}C years, but this value arises from the mixing of differently-aged components, and therefore significant amounts of organic matter older than the average value are present in the samples. Although topsoil erosion is probably the major source of the riverine POM, the average PO{sup 14}C value is appreciably lower than topsoil values (which are typically 100 pMC). This is most likely explained by inputs of older subsoil OC from bank erosion, or the preferential loss of high-{sup 14}C topsoil organic matter by mineralisation during riverine transport. The significantly lower average PO{sup 14}C of samples from the River Calder (76.6 pMC), can be ascribed to components containing little or no radiocarbon, derived either from industrial sources or historical coal mining, and this effect is also seen in the River Ribble, downstream of its confluence with the Calder. At the global scale, the results significantly expand available information for PO{sup 14}C in rivers draining catchments with low erosion rates

Improvements in PIXE analysis of hourly particulate matter samples

Energy Technology Data Exchange (ETDEWEB)

Calzolai, G., E-mail: calzolai@fi.infn.it [Department of Physics and Astronomy, University of Florence, Via G. Sansone 1, 50019 Sesto Fiorentino (Italy); National Institute of Nuclear Physics (INFN), Division of Florence, Via G. Sansone 1, 50019 Sesto Fiorentino (Italy); Lucarelli, F. [Department of Physics and Astronomy, University of Florence, Via G. Sansone 1, 50019 Sesto Fiorentino (Italy); National Institute of Nuclear Physics (INFN), Division of Florence, Via G. Sansone 1, 50019 Sesto Fiorentino (Italy); Chiari, M.; Nava, S. [National Institute of Nuclear Physics (INFN), Division of Florence, Via G. Sansone 1, 50019 Sesto Fiorentino (Italy); Giannoni, M. [National Institute of Nuclear Physics (INFN), Division of Florence, Via G. Sansone 1, 50019 Sesto Fiorentino (Italy); Department of Chemistry, University of Florence, Via della Lastruccia 3, 50019 Sesto Fiorentino (Italy); Carraresi, L. [Department of Physics and Astronomy, University of Florence, Via G. Sansone 1, 50019 Sesto Fiorentino (Italy); National Institute of Nuclear Physics (INFN), Division of Florence, Via G. Sansone 1, 50019 Sesto Fiorentino (Italy); Prati, P. [Department of Physics, University of Genoa and INFN Division of Genoa, Via Dodecaneso 33, 16146 Genoa (Italy); Vecchi, R. [Department of Physics, Università degli Studi di Milano and INFN Division of Milan, Via Celoria 16, 20133 Milan (Italy)

2015-11-15

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.

Samplings of urban particulate matter for mutagenicity assays; Campionamenti di particolato atmosferico in area urbana per valutazioni di potenziale mutageno

Energy Technology Data Exchange (ETDEWEB)

De Zaiacomo, T. [ENEA, Centro Ricerche Bologna (Italy). Dip. Ambiente

1996-07-01

In the frame of a specific program relating to the evaluation of mutagenic activity of urban particulate matter, an experimental arrangement has been developed to sample aerosuspended particles from the external environment carried indoor by means of a fan. Instrumentation was placed directly in the air flow to minimize particle losses, and consisted of total filter, collecting particles without any size separation; cascade impactor, fractioning urban particulate to obtain separate samples for analyses; an optical device, for real time monitoring of aerosol concentration, temperature and relative humidity sensors. Some of the samples obtained were analysed to investigate: particle morphology, aerosol granulometric distributions, effect of relative humidity on collected particulate, amount of ponderal mass compared with real time optical determinations. The results obtained are reported here, together with some considerations about carbonaceous particles, in urban areas mainly originated from diesel exhausts, their degree of agglomeration and role to vehiculate substances into the human respiratory.

Characterization of airborne particulate matter in Santiago, Chile. Part 1: design, sampling and analysis for an experimental campaign

International Nuclear Information System (INIS)

Toro E, P.

1995-01-01

This work describes the siting and sampling procedures of collecting airborne particulate matter in Santiago, Chile, determining its chemical composition and daily behaviour. The airborne particulate matter was collected onto polycarbonate membranes, one of fine pore and other of coarse pore, using Pm 10 samplers. The material was analyzed using neutron activation analysis., proton induced X ray emission, X ray fluorescence, voltametry, atomic absorption spectrometry, ion chromatography and isotope dilution. (author). 1 tab

Chemical Composition and Emission Sources of the Fine Particulate Matters in a Southeast Asian Mega City (Dhaka, Bangladesh)

Science.gov (United States)

Salam, Abdus

2016-04-01

Air pollution has significant impact on human health, climate change, agriculture, visibility reduction, and also on the atmospheric chemistry. There are many studies already reported about the direct relation of the human mortality and morbidity with the increase of the atmospheric particulate matters. Especially, fine particulate matters can easily enter into the human respiratory system and causes many diseases. Particulate matters have the properties to absorb the solar radiation and impact on the climate. Dhaka, Bangladesh is a densely populated mega-city in the world. About 16 million inhabitants are living within an area of 360 square kilometers. Air quality situation has been degrading due to unplanned growth, increasing vehicles, severe traffic jams, brick kilns, industries, construction, and also transboundary air pollution. A rapidly growing number of vehicles has worsen the air quality in spite of major policy interventions, e.g., ban of two-stroke and three-wheeled vehicles, phase out of 20 years old vehicles, conversion to compressed natural gas (CNGs), etc. Introduction of CNGs to reduce air pollution was not the solution for fine particles at all, as evidence shows that CNGs and diesel engines are the major sources of fine particles. High concentration of the air pollutants in Dhaka city such as PM, carbonaceous species (black and organic carbon), CO, etc. has already been reported. PM2.5 mass, chemical composition (e.g., BC, OC, SO42-, NO3-, trace elements, etc.), aerosol Optical Depth (AOD) and emission sources of our recent measurements at the highly polluted south East Asian Mega city (Dhaka) Bangladesh will be presented in the conference. PM2.5 samples were collected on filters with Digital PM2.5 sampler (Switzerland) and Air photon, USA. BC was measured from filters (with thermal and optical method) and also real time with an Aethalometer AE42 (Magee Scitific., USA). Water soluble ions were determined from filters with ion chromatogram. AOD

Controlling particulate matter under the Clean Air Act: a menu of options

Energy Technology Data Exchange (ETDEWEB)

NONE

1996-07-01

This document was prepared by STAPPA and ALAPCO to help US state and local air pollution control officials understand the effects of particulate matter (PM) on human health and air quality, the relative contribution of various sources to particulate emissions, and the effectiveness and costs of various approaches - including innovative ones - to minimizing these emissions. The document covers particulate matter with a nominal diameter of 10 microns ({mu}m) or less (PM{sub 10}), including `fine` PM of 2.5 microns or less in diameter (PM{sub 2.5}). Sections cover: the effects of particulate matter on human health; regulatory issues; characterization of particulate matter; emission control strategies for mobile sources (diesel engines, small nonroad engines, alternative fuels etc.), particulates from stationary sources (electric utilities, industry and commercial fuel combustion; mineral products industry, metallurgical industry etc.); particulates from area sources; and market-based strategies for controlling particulate matter. 2 apps.

Sampling of suspended particulate matter using particle traps in the Rhône River: Relevance and representativeness for the monitoring of contaminants.

Science.gov (United States)

Masson, M; Angot, H; Le Bescond, C; Launay, M; Dabrin, A; Miège, C; Le Coz, J; Coquery, M

2018-05-10

Monitoring hydrophobic contaminants in surface freshwaters requires measuring contaminant concentrations in the particulate fraction (sediment or suspended particulate matter, SPM) of the water column. Particle traps (PTs) have been recently developed to sample SPM as cost-efficient, easy to operate and time-integrative tools. But the representativeness of SPM collected with PTs is not fully understood, notably in terms of grain size distribution and particulate organic carbon (POC) content, which could both skew particulate contaminant concentrations. The aim of this study was to evaluate the representativeness of SPM characteristics (i.e. grain size distribution and POC content) and associated contaminants (i.e. polychlorinated biphenyls, PCBs; mercury, Hg) in samples collected in a large river using PTs for differing hydrological conditions. Samples collected using PTs (n = 74) were compared with samples collected during the same time period by continuous flow centrifugation (CFC). The grain size distribution of PT samples shifted with increasing water discharge: the proportion of very fine silts (2-6 μm) decreased while that of coarse silts (27-74 μm) increased. Regardless of water discharge, POC contents were different likely due to integration by PT of high POC-content phytoplankton blooms or low POC-content flood events. Differences in PCBs and Hg concentrations were usually within the range of analytical uncertainties and could not be related to grain size or POC content shifts. Occasional Hg-enriched inputs may have led to higher Hg concentrations in a few PT samples (n = 4) which highlights the time-integrative capacity of the PTs. The differences of annual Hg and PCB fluxes calculated either from PT samples or CFC samples were generally below 20%. Despite some inherent limitations (e.g. grain size distribution bias), our findings suggest that PT sampling is a valuable technique to assess reliable spatial and temporal trends of particulate

Evaluation of airborne particulate matter pollution in Kenitra City, Morocco

Directory of Open Access Journals (Sweden)

Abdelfettah Benchrif

2013-04-01

Full Text Available Two size fractions of atmospheric particulate matter < 2.5 µm and 2.5-10 µm were collected in Kenitra City from February 2007 to February 2008. The sampling was done using a Gent Stacked sampler on nuclepore polycarbonate filters and the collected filters were analyzed using Total Reflection X-Ray Fluorescence (TXRF and Atomic Absorption Spectroscopy (AAS. The particulate matter trends show higher concentrations during the summer as compared to other seasons. The highest concentrations were obtained for Ca in coarse particles and Fe for fine particles. However, the lowest concentrations were observed for Cd in both particulate sizes. The principal component analysis (PCA based on multivariate study enabled the identification of soil, road dust and traffic emissions as common sources for coarse and fine particles.

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

International Nuclear Information System (INIS)

Mazurek, M.A.; Hildemann, L.M.; Simoneit, B.R.T.

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

Composition and Sources of Particulate Matter Measured near Houston, TX: Anthropogenic-Biogenic Interactions

Directory of Open Access Journals (Sweden)

Jeffrey K. Bean

2016-05-01

Full Text Available Particulate matter was measured in Conroe, Texas (~60 km north of downtown Houston, Texas during the September 2013 DISCOVER-AQ campaign to determine the sources of particulate matter in the region. The measurement site is influenced by high biogenic emission rates as well as transport of anthropogenic pollutants from the Houston metropolitan area and is therefore an ideal location to study anthropogenic-biogenic interactions. Data from an Aerosol Chemical Speciation Monitor (ACSM suggest that on average 64 percent of non-refractory PM1 was organic material, including a high fraction (27%–41% of organic nitrates. There was little diurnal variation in the concentrations of ammonium sulfate; however, concentrations of organic and organic nitrate aerosol were consistently higher at night than during the day. Potential explanations for the higher organic aerosol loadings at night include changing boundary layer height, increased partitioning to the particle phase at lower temperatures, and differences between daytime and nighttime chemical processes such as nitrate radical chemistry. Positive matrix factorization was applied to the organic aerosol mass spectra measured by the ACSM and three factors were resolved—two factors representing oxygenated organic aerosol and one factor representing hydrocarbon-like organic aerosol. The factors suggest that the measured aerosol was well mixed and highly processed, consistent with the distance from the site to major aerosol sources, as well as the high photochemical activity.

Small-angle light scattering by airborne particulates: Environnement S.A. continuous particulate monitor

International Nuclear Information System (INIS)

Renard, Jean-Baptiste; Gaubicher, Bertrand; Thaury, Claire; Mineau, Jean-Luc

2010-01-01

Airborne particulate matter may have an effect on human health. It is therefore necessary to determine and control in real time the evolution of the concentration and mass of particulates in the ambient air. These parameters can be obtained using optical methods. We propose here a new instrument, 'CPM' (continuous particulate monitor), for the measurement of light scattered by ambient particulates at small angles. This geometry allows simultaneous and separate detections of PM10, PM2.5 and PM1 fractions of airborne particulate matter, with no influence of their chemical nature and without using theoretical calculations. The ambient air is collected through a standard sampling head (PM10 inlet according to EN 12341, PM2.5 inlet according to EN 14907; or PM1, TSP inlets, standard US EPA inlets). The analysis of the first measurements demonstrates that this new instrument can detect, for each of the seven defined size ranges, real-time variations of particulate content in the ambient air. The measured concentrations (expressed in number per liter) can be converted into total mass concentrations (expressed in micrograms per cubic meter) of all fractions of airborne particulate matters sampled by the system. Periodic comparison with a beta-attenuation mass monitor (MP101M Beta Gauge Analyzer from Environnement S.A. company) allows the calculation of a calibration factor as a function of the mean particulate density that is used for this conversion. It is then possible to provide real-time relative variations of aerosol mass concentration

PCDD/PCDF and dl-PCB in the ambient air of a tropical Andean city: passive and active sampling measurements near industrial and vehicular pollution sources.

Science.gov (United States)

Cortés, J; González, C M; Morales, L; Abalos, M; Abad, E; Aristizábal, B H

2014-09-01

Concentration gradients were observed in gas and particulate phases of PCDD/F originating from industrial and vehicular sources in the densely populated tropical Andean city of Manizales, using passive and active air samplers. Preliminary results suggest greater concentrations of dl-PCB in the mostly gaseous fraction (using quarterly passive samplers) and greater concentrations of PCDD/F in the mostly particle fraction (using daily active samplers). Dioxin-like PCB predominance was associated with the semi-volatility property, which depends on ambient temperature. Slight variations of ambient temperature in Manizales during the sampling period (15°C-27°C) may have triggered higher concentrations in all passive samples. This was the first passive air sampling monitoring of PCDD/F conducted in an urban area of Colombia. Passive sampling revealed that PCDD/F in combination with dioxin-like PCB ranged from 16 WHO-TEQ2005/m(3) near industrial sources to 7 WHO-TEQ2005/m(3) in an intermediate zone-a reduction of 56% over 2.8 km. Active sampling of particulate phase PCDD/F and dl-PCB were analyzed in PM10 samples. PCDD/F combined with dl-PCB ranged from 46 WHO-TEQ2005/m(3) near vehicular sources to 8 WHO-TEQ2005/m(3) in the same intermediate zone, a reduction of 83% over 2.6 km. Toxic equivalent quantities in both PCDD/F and dl-PCB decreased toward an intermediate zone of the city. Variations in congener profiles were consistent with variations expected from nearby sources, such as a secondary metallurgy plant, areas of concentrated vehicular emissions and a municipal solid waste incinerator (MSWI). These variations in congener profile measurements of dioxins and dl-PCBs in passive and active samples can be partly explained by congener variations expected from the various sources. Copyright © 2014 Elsevier B.V. All rights reserved.

An economic passive sampling method to detect particulate pollutants using magnetic measurements.

Science.gov (United States)

Cao, Liwan; Appel, Erwin; Hu, Shouyun; Ma, Mingming

2015-10-01

Identifying particulate matter (PM) emitted from industrial processes into the atmosphere is an important issue in environmental research. This paper presents a passive sampling method using simple artificial samplers that maintains the advantage of bio-monitoring, but overcomes some of its disadvantages. The samplers were tested in a heavily polluted area (Linfen, China) and compared to results from leaf samples. Spatial variations of magnetic susceptibility from artificial passive samplers and leaf samples show very similar patterns. Scanning electron microscopy suggests that the collected PM are mostly in the range of 2-25 μm; frequent occurrence of spherical shape indicates industrial combustion dominates PM emission. Magnetic properties around power plants show different features than other plants. This sampling method provides a suitable and economic tool for semi-quantifying temporal and spatial distribution of air quality; they can be installed in a regular grid and calibrate the weight of PM. Copyright © 2015 Elsevier Ltd. All rights reserved.

Toward Distinguishing Woodsmoke and Diesel Exhaust in Ambient Particulate Matter

International Nuclear Information System (INIS)

Braun, A.; Huggins, F.; Kubatova, A.; Wirick, S.; Maricq, M.; Mun, B.; McDonald, J.; Kelly, K.; Shah, N.; Huffman, G.

2008-01-01

Particulate matter (PM) from biomass burning and diesel exhaust has distinct X-ray spectroscopic, carbon specific signatures, which can be employed for source apportionment. Characterization of the functional groups of a wide selection of PM samples (woodsmoke, diesel soot, urban air PM) was carried out using the soft X-ray spectroscopy capabilities at the synchrotron radiation sources in Berkeley (ALS) and Brookhaven (NSLS). The spectra reveal that diesel exhaust particulate (DEP) matter is made up from a semigraphitic solid core and soluble organic matter, predominantly with carboxylic functional groups. Woodsmoke PM has no or a less prevalent, graphitic signature, instead it contains carbon-hydroxyl groups. Using these features to apportion the carbonaceous PM in ambient samples we estimate that the relative contribution of DEP to ambient PM in an urban area such as Lexington, KY and St. Louis, MO is 7% and 13.5%, respectively. These values are comparable to dispersion modeling data from nonurban and urban areas in California, and with elemental carbon measurements in urban locations such as Boston, MA, Rochester, NY, and Washington, DC.

Study of particulate matter in Limeira (Brazil) using SR-TXRF

International Nuclear Information System (INIS)

Canteras, Felippe B.; Moreira, Silvana

2011-01-01

Air pollution is a growing problem mainly in metropolitan areas in the world. The atmospheric pollutants are responsible for various environmental problems including the human health. Among the pollutants, the particulate matter is important, since it has a heterogeneous composition. The goal of this work was to analyze quantitatively the particulate matter in Limeira city, Sao Paulo State, Brazil. The sampling was made using a sequential filtering system, containing two filters putted in series, to collect fine and coarse fractions. After a removal in an acid medium, with ultrasound bath, the samples were analyzed by Synchrotron Radiation Total Reflection X-Ray Fluorescence (SR-TXRF). The results obtained for PM10 were in agreement with the standards defined by the Brazilian legislation and also with the standards established by USEPA. In all analyzed samples S, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Br, Rb, Sr, Ba and Pb were quantified. Employing multivariate statistical analysis (principal component and cluster analysis) was possible to identify the emission sources. For coarse fraction the main emission source was soil dusty responsible for 57% of the total in the coarse fraction, followed by vehicular emission with 30% and industrial 13%. In the fine fraction soil dusty was the mainly emission source contributing with 79% of the total, followed by vehicular emission with 13% and finally the industrial emission responsible just for 8%. (author)

Study of particulate matter in Limeira (Brazil) using SR-TXRF

Energy Technology Data Exchange (ETDEWEB)

Canteras, Felippe B.; Moreira, Silvana, E-mail: silvana@fec.unicamp.b [Universidade Estadual de Campinas (FEC/UNICAMP), SP (Brazil) Faculdade de Engenharia Civil, Arquitetura e Urbanismo

2011-07-01

Air pollution is a growing problem mainly in metropolitan areas in the world. The atmospheric pollutants are responsible for various environmental problems including the human health. Among the pollutants, the particulate matter is important, since it has a heterogeneous composition. The goal of this work was to analyze quantitatively the particulate matter in Limeira city, Sao Paulo State, Brazil. The sampling was made using a sequential filtering system, containing two filters putted in series, to collect fine and coarse fractions. After a removal in an acid medium, with ultrasound bath, the samples were analyzed by Synchrotron Radiation Total Reflection X-Ray Fluorescence (SR-TXRF). The results obtained for PM10 were in agreement with the standards defined by the Brazilian legislation and also with the standards established by USEPA. In all analyzed samples S, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Br, Rb, Sr, Ba and Pb were quantified. Employing multivariate statistical analysis (principal component and cluster analysis) was possible to identify the emission sources. For coarse fraction the main emission source was soil dusty responsible for 57% of the total in the coarse fraction, followed by vehicular emission with 30% and industrial 13%. In the fine fraction soil dusty was the mainly emission source contributing with 79% of the total, followed by vehicular emission with 13% and finally the industrial emission responsible just for 8%. (author)

Analysis of Phytosterols and N-Alkanols in Atmospheric Organic Particulate Matter Collected in Vancouver During the Pacific 2001 Air Quality Study

Science.gov (United States)

Leithead, A.; Li, S.

2002-12-01

As part of Pacific 2001, HiVol samples were collected from 5 sites in the Vancouver area. The samples were extracted by accelerated solvent extraction (ACE), concentrated with nitrogen blow down, and separated into fractions by silica gel chromatography. For this portion of the study, an aliquot of one of the polar fraction was derivatized with BSTFA and analyzed by GC-FID and GC-MS. The results for n-alkanols and phytosterols will be reported and discussed. Previous studies have shown that the biogenic components of particulate matter are major constituents of the total organic material in atmospheric samples. Phytosterols are present in wood smoke, epicuticular waxes of many plants and microbial sources. In addition, cholesterol has been proposed as a potential tracer for emissions from cooking. The most abundant phytosterols are cholesterol, campesterol, stigmasterol and beta-sitosterol. It has been hypothesized that the phytosterol signature may be useful in identifying particulate matter from different source areas. The phytosterol signature for these samples will be reported and compared. The n-alkanol CPI and Cmax will also be reported. N-alkanols in atmospheric samples generally show a strong even to odd predominance indicating that their main source in particulate matter is biogenic. The n-alkanol signature for each sampling site will be compared.

Mass spectroscopic analysis of atmospheric particulate matter

International Nuclear Information System (INIS)

Wippel, R.

1997-02-01

Particulate matter (PM) in the atmosphere vary greatly in origin, in their physical and chemical properties and their effects on climate, atmospheric chemistry and health. Aerosol particles with an aerodynamic diameter less than two μm can enter the respiratory tract of humans when inhaled. Bulk analysis of ambient dust particles was performed using an inductively coupled plasma mass spectrometer (ICP-MS). The size-fractionated collected samples were analyzed after a leaching procedure that simulates the solution reactions occurring in the lungs. A disadvantage of bulk analysis is that it gives no information about the distribution of a certain element within the particles under investigation. A Laser-Microprobe-Mass-Analyzer (LAMMA-500) was used to obtain this information. At sampling sites in Austria and in Zimbabwe, Africa, single particles were sampled using a self-made impactor. One of the final aims in environmental analysis is to successfully apply receptor models that relate the chemical and physical properties of a receptor site to a source. The knowledge of the sources of atmospheric particulate matter is essential for environmental policy makers as well as for epidemiological studies. Artificial neural networks (ANN) have a remarkable ability to handle LAMMA-data. Three ANNs were used as a pattern recognition tool for LAMMA mass spectral data: a back-propagation net, a Kohonen network,and a counter-propagation net. Standard source profiles from the United States Environmental Protection Agency were used as training and test data of the different nets. The elemental patterns of the sum of 100 mass spectra of fine dust particles were presented to the trained nets and satisfactory recognition (> 80 %) was obtained. (author)

Results of Self-Absorption Study on the Versapor 3000 Filters for Radioactive Particulate Air Sampling

International Nuclear Information System (INIS)

Barnett, J.M.; Cullinan, Valerie I.; Barnett, Debra S.; Trang-Le, Truc LT; Bliss, Mary; Greenwood, Lawrence R.; Ballinger, Marcel Y.

2009-01-01

Since the mid-1980s, Pacific Northwest National Laboratory (PNNL) has used a value of 0.85 as the correction factor for self absorption of activity for particulate radioactive air samples collected from building exhaust for environmental monitoring. This value accounts for activity that cannot be detected by direct counting of alpha and beta particles. Emissions can be degraded or blocked by filter fibers for particles buried in the filter material or by inactive dust particles collected with the radioactive particles. These filters are used for monitoring air emissions from PNNL stacks for radioactive particles. This paper describes an effort to re-evaluate self-absorption effects in particulate radioactive air sample filters (Versapor(reg s ign) 3000, 47 mm diameter) used at PNNL. There were two methods used to characterize the samples. Sixty samples were selected from the archive for acid digestion to compare the radioactivity measured by direct gas-flow proportional counting of filters to the results obtained after acid digestion of the filter and counting again by gas-flow proportional detection. Thirty different sample filters were selected for visible light microscopy to evaluate filter loading and particulate characteristics. Mass-loading effects were also considered. Filter ratios were calculated by dividing the initial counts by the post-digestion counts with the expectation that post-digestion counts would be higher because digestion would expose radioactivity embedded in the filter in addition to that on top of the filter. Contrary to expectations, the post digestion readings were almost always lower than initial readings and averaged approximately half the initial readings for both alpha and beta activity. Before and after digestion readings appeared to be related to each other, but with a low coefficient of determination (R 2 ) value. The ratios had a wide range of values indicating that this method did not provide sufficient precision to quantify

Characterization of airborne particulate matter in the metropolitan region of Belo Horizonte

International Nuclear Information System (INIS)

Tavares, Fernanda V.F.; Ardisson, Jose Domingos; Rodrigues, Paulo Cesar H.; Brito, Walter de; Macedo, Waldemar Augusto A.; Jacomino, Vanusa Maria F.

2013-01-01

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 57 Fe-Moessbauer 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. 57 Fe-Moessbauer 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. (author)

Comparison of PIXE and XRF analysis of airborne particulate matter samples collected on Teflon and quartz fibre filters

Science.gov (United States)

Chiari, M.; Yubero, E.; Calzolai, G.; Lucarelli, F.; Crespo, J.; Galindo, N.; Nicolás, J. F.; Giannoni, M.; Nava, S.

2018-02-01

Within the framework of research projects focusing on the sampling and analysis of airborne particulate matter, Particle Induced X-ray Emission (PIXE) and Energy Dispersive X-ray Fluorescence (ED-XRF) techniques are routinely used in many laboratories throughout the world to determine the elemental concentration of the particulate matter samples. In this work an inter-laboratory comparison of the results obtained from analysing several samples (collected on both Teflon and quartz fibre filters) using both techniques is presented. The samples were analysed by PIXE (in Florence, at the 3 MV Tandetron accelerator of INFN-LABEC laboratory) and by XRF (in Elche, using the ARL Quant'X EDXRF spectrometer with specific conditions optimized for specific groups of elements). The results from the two sets of measurements are in good agreement for all the analysed samples, thus validating the use of the ARL Quant'X EDXRF spectrometer and the selected measurement protocol for the analysis of aerosol samples. Moreover, thanks to the comparison of PIXE and XRF results on Teflon and quartz fibre filters, possible self-absorption effects due to the penetration of the aerosol particles inside the quartz fibre-filters were quantified.

Aerotrace. Measurement of particulates from an engine combustor

Energy Technology Data Exchange (ETDEWEB)

Hurley, C D [DRA, Farnborough (United Kingdom)

1998-12-31

The effect of gas turbine operating conditions, inlet temperature, pressure and overall air fuel ratio, on particulate number density has been measured. Particulate number density was found to be proportional to combustor inlet pressure and decrease with increasing combustor inlet temperature. The relationship with air fuel ratio is more complex. The mechanism of particulate loss down sample lines has been elucidated and equations are presented to predict particulate losses for stainless steel and PTFE sample lines. (author) 3 refs.

Aerotrace. Measurement of particulates from an engine combustor

Energy Technology Data Exchange (ETDEWEB)

Hurley, C.D. [DRA, Farnborough (United Kingdom)

1997-12-31

The effect of gas turbine operating conditions, inlet temperature, pressure and overall air fuel ratio, on particulate number density has been measured. Particulate number density was found to be proportional to combustor inlet pressure and decrease with increasing combustor inlet temperature. The relationship with air fuel ratio is more complex. The mechanism of particulate loss down sample lines has been elucidated and equations are presented to predict particulate losses for stainless steel and PTFE sample lines. (author) 3 refs.

Emission characteristics and chemical components of size-segregated particulate matter in iron and steel industry

Science.gov (United States)

Jia, Jia; Cheng, Shuiyuan; Yao, Sen; Xu, Tiebing; Zhang, Tingting; Ma, Yuetao; Wang, Hongliang; Duan, Wenjiao

2018-06-01

As one of the highest energy consumption and pollution industries, the iron and steel industry is regarded as a most important source of particulate matter emission. In this study, chemical components of size-segregated particulate matters (PM) emitted from different manufacturing units in iron and steel industry were sampled by a comprehensive sampling system. Results showed that the average particle mass concentration was highest in sintering process, followed by puddling, steelmaking and then rolling processes. PM samples were divided into eight size fractions for testing the chemical components, SO42- and NH4+ distributed more into fine particles while most of the Ca2+ was concentrated in coarse particles, the size distribution of mineral elements depended on the raw materials applied. Moreover, local database with PM chemical source profiles of iron and steel industry were built and applied in CMAQ modeling for simulating SO42- and NO3- concentration, results showed that the accuracy of model simulation improved with local chemical source profiles compared to the SPECIATE database. The results gained from this study are expected to be helpful to understand the components of PM in iron and steel industry and contribute to the source apportionment researches.

Source apportionment of carbonaceous particulate matter during haze days in Shanghai based on the radiocarbon

International Nuclear Information System (INIS)

Nannan Wei; Jialiang Feng; Detao Xiao

2017-01-01

To estimate the sources of carbonaceous particulate matter, "1"4C and biomass-burning marker (levoglucosan) were measured in the form of organic carbon (OC) and elemental carbon (EC) in PM_2_._5 that was collected in five different functional districts of Shanghai during winter 2013. Spatial variations of the contemporary proportion among different districts were evident. The results of levoglucosan in Xujiahui (XH) and Chongming (CM) agreed well with those of "1"4C. The results indicate that environmental protection policies should vary for functional districts within the same city to account for their different sources of emissions. (author)

Mobile sources of polycyclic aromatic hydrocarbons (PAH) and nitro-PAH: Results of samples collected in a roadway tunnel

International Nuclear Information System (INIS)

Benner, B.A. Jr.; Gordon, G.E.; Wise, S.A.

1987-01-01

A recent review article emphasized the need for further characterizations of the carbonaceous fraction of mobile source emissions, particularly with the impending removal of lead alkyl octane boosters and bromine-containing lead scavengers from regular leaded gasolines. The lead and bromine emitted from the combustion of these fuels have been used as tracers of mobile source emissions for a number of years. Single vehicle emission studies have shed light on the relationship between engine operating parameters and the chemical characteristics of the emissions but they are not suitable for use in source apportionment studies which require emission data from a large number of different vehicles. Air particulate samples collected near a busy highway or in a roadway tunnel would be more appropriate for use in estimating the mobile source contribution of organic compounds to a region. Suspended particle samples collected in a heavily-travelled roadway tunnel (Baltimore Harbor Tunnel, Baltimore, Maryland) were characterized for polycyclic aromatic hydrocarbons (PAH) and some nitro-PAH by gas and liquid chromatographic techniques. These samples included those collected on Teflon filters and on glass fiber filters for investigating any differences in samples collected on an inert (Teflon) and more reactive (glass-fiber) medium. All samples collected on Teflon were backed-up with polyurethane foam plugs (PUF) which trapped any inherent vapor-phase PAH as well as any compounds ''blown-off'' the particles during collection

The particulate matter dispersion studies from a local palm oil mill

International Nuclear Information System (INIS)

Abdullah, L.C.; Wong, L. L.; Amnorzahira, A.; Sa'ari, M.; Abdul Rashid, M. S.; Salmiaton Ali

2006-01-01

The appearance of industrial emissions and the degradation of scenic vistas are two characteristics of air pollution that humans object. Reduction in visibility suggests worsening pollution levels. The emissions from mobile source and stationary source are the major source of air pollutions contribution in Malaysia. Suspended particulate matter (SPM). The consequence of increasing the particulate concentrations, the particulate matter dissolves with vapour and grows into droplets when the humidity exceeds approximately 70% and causing opaque situation know as haze. This work focuses on the dispersion particulate matter from palm oil mill. The data obtained serves the purpose of modeling the transport of particulate matter for obtaining permits and prevention of significant deterioration (PSD) to the environment. Gaussian Plume Model from a point source, subject to various atmospheric conditions is used to calculate particulate matter concentration then display the distribution of plume dispersion using geographic information system (GIS). The calculated particulate matter concentration is evaluated using Transilient Matrice function. Atmospheric Stability, mixing height, wind direction, wind speed, natural and artificial features play an important role in dispersion process. High concentration area exhibits immediately under prevailing wind direction. (Author)

Characterization of particulate amines

International Nuclear Information System (INIS)

Gundel, L.A.; Chang, S.G.; Clemenson, M.S.; Markowitz, S.S.; Novakov, T.

1979-01-01

The reduced nitrogen compounds associated with ambient particulate matter are chemically characterized by means of ESCA and proton activation analysis. Ambient particulate samples collected on silver filters in Berkeley, California were washed with water and organic solvents, and ESCA and proton activation analysis were performed in order to determine the composition of various nitrogen compounds and the total nitrogen content. It is found that 85% of the amines originally present in ambient particulate matter can be removed by water extraction, whereas the ammonium and nitrate are completely removed. An observed increase in ammonium ion in the extract, compared with its concentration in the original sample, coupled with the commensurate decrease in amine concentration, is attributed to the hydrolysis of amide groups, which may cause analytical methods based on extraction to yield erroneous results

Size, Composition, and Sources of Health Relevant Particulate Matter in the San Joaquin Valley

Science.gov (United States)

Ham, Walter Allan

Particulate Matter (PM) is an environment contaminant that has been associated with adverse health effects in epidemiological and toxicological studies. Atmospheric PM is made up of a diverse array of chemical species that are emitted from multiple sources across a range of aerodynamic diameters spanning several orders of magnitude. The focus of the present work was the characterization of ambient PM with aerodynamic diameters below 1.8 mum (PM1.8) in 6 size sub-fractions including PM0.1. Chemical species measured included organic carbon, elemental carbon, water soluble ions, trace metals, and organic molecular markers in urban and rural environments in the San Joaquin Valley. These measurements were used to determine differences in relative diurnal size distributions during a severe winter stagnation event, seasonal changes in PM size and composition, and the source origin of carbonaceous PM. This size-resolved information was used to calculate lung deposition patterns of health relevant PM species to evaluate seasonal differences in PM dose. By accurately calculating PM dose, researchers are able to more directly link ambient PM characterization data with biological endpoints. All of these results are used to support ongoing toxicological health effects studies. These types of analyses are important as this type of information may assist regulators with developing control strategies to reduce health effects caused by particulate air pollution.

PM10 sampler deposited air particulates: Ascertaining uniformity of sample on filter through rotated exposure to radiation

International Nuclear Information System (INIS)

Owoade, Oyediran K.; Olise, Felix S.; Obioh, Imoh B.; Olaniyi, Hezekiah B.; Bolzacchini, Ezio; Ferrero, Luca; Perrone, Grazia

2006-01-01

For reproducibility of analytical results of samples deposited on filters using PM 10 sampler, homogeneity of the sample on the filter is very important especially when the size of the X-ray beam for the analysis is less than the size of filter. It is against this background that the air particulate samples collected on using PM 10 samplers are analysed to determine the elemental concentrations. Each sample was divided into four quadrants and each was analysed under same conditions to determine if the particles were deposited uniformly over the filter. Each analysis was done using EDXRF technique. The spectrometer consists of four secondary targets, which are automatically switched to in sequence in analysing each sample. The concentration of various elements detected was determined using TURBOQUANT (a brand name for a SPECTRO method which is used for screening analysis). Sixteen elements were detected in every sample. Results show that there was less than 10% deviation in the concentrations in different quadrants. There were a few elements like Ba, Cs, etc., which have deviation greater than 20%. The concentrations of these latter elements were close to detection limits of the spectrometer. We conclude that the analytical result of particulate samples deposited on filters by the PM 10 sampler can be reliable in terms of the homogeneity of the deposition. For such analytes with low concentrations, it would be important that the sampling time be increased to allow for higher mass deposition on the filter

Source contribution analysis of surface particulate polycyclic aromatic hydrocarbon concentrations in northeastern Asia by source–receptor relationships

International Nuclear Information System (INIS)

Inomata, Yayoi; Kajino, Mizuo; Sato, Keiichi; Ohara, Toshimasa; Kurokawa, Jun-ichi; Ueda, Hiromasa; Tang, Ning; Hayakawa, Kazuichi; Ohizumi, Tsuyoshi; Akimoto, Hajime

2013-01-01

We analyzed the source–receptor relationships for particulate polycyclic aromatic hydrocarbon (PAH) concentrations in northeastern Asia using an aerosol chemical transport model. The model successfully simulated the observed concentrations. In Beijing (China) benzo[a]pyren (BaP) concentrations are due to emissions from its own domain. In Noto, Oki and Tsushima (Japan), transboundary transport from northern China (>40°N, 40–60%) and central China (30–40°N, 10–40%) largely influences BaP concentrations from winter to spring, whereas the relative contribution from central China is dominant (90%) in Hedo. In the summer, the contribution from Japanese domestic sources increases (40–80%) at the 4 sites. Contributions from Japan and Russia are additional source of BaP over the northwestern Pacific Ocean in summer. The contribution rates for the concentrations from each domain are different among PAH species depending on their particulate phase oxidation rates. Reaction with O 3 on particulate surfaces may be an important component of the PAH oxidation processes. -- Highlights: •Source–receptor analysis was conducted for investigating PAHs in northeast Asia. •In winter, transboundary transport from China is large contribution in leeward. •Relative contribution from Korea, Japan, and eastern Russia is increased in summer. •This seasonal variation is strongly controlled by the meteorological conditions. •The transport distance is different among PAH species. -- Transboundary transport of PAHs in northeast Asia was investigated by source–receptor analysis

Establishing aeolian particulate 'fingerprints' in an airport environment using magnetic measurements and SEM/EDAX

Science.gov (United States)

Jones, Sue; Hoon, Stephen R.; Richardson, Nigel; Bennett, Michael

2016-04-01

The significant increase in global air travel which has occurred during the last fifty years has generated growing concern regarding the potential impacts associated with increasing emissions of particulate matter (PM) from aviation activity on health and the environment. PM within the airport environment, in particular, may be derived from a wide range of potential sources including aircraft; vehicles; ground support equipment and buildings. In order to investigate and remediate potential problem sources, it is important to be able to identify characteristic particulate 'fingerprints' which would allow source attribution, particularly respirable particulates. To date the identification of such 'fingerprints' has remained elusive but remains a key research priority for the aviation industry (Webb et al, 2008). In previous PM studies, environmental magnetism has been used as a successful technique for discriminating between different emission types and particulate sources in both urban and industrial environments (e.g. Hunt et al 1984; Lecoanet et al 2003, Jones et al 2015). Environmental magnetism is a non-destructive and relatively rapid technique involving the use of non-directional, rock magnetic measurements to characterise the mineral magnetic properties of natural and anthropogenic materials. In other studies scanning electron microscopy (SEM) has also been used as an effective characterisation technique for the investigation of grain size and morphology of PM derived from vehicle emissions (e.g. Bucko et al 2010) and fossil fuel combustion sources (Kim et al 2009). In this study, environmental magnetic measurements and SEM/EDAX have been used to characterise dusts from specific aircraft sources including engines, brakes and tyres. Furthermore, these methods have also been applied to runway (both hard and grass covered surfaces), taxiway and apron dusts collected during extensive environmental sampling at Manchester International Airport, UK in order to

Polycyclic aromatic hydrocarbons in suspended particulate matter and sediments from the Pearl River Estuary and adjacent coastal areas, China

International Nuclear Information System (INIS)

Luo Xiaojun; Chen Shejun; Mai Bixian; Yang Qingshu; Sheng Guoying; Fu Jiamo

2006-01-01

The spatial distribution, composition, and sources of polycyclic aromatic hydrocarbons (PAHs) in sediments and suspended particulate matter (SPM) from the Pearl River Estuary and adjacent coastal areas were examined. Total PAH concentrations varied from 189 to 637 ng/g in sediments and 422 to 1850 ng/g in SPM. PAHs were dominated by 5,6-ring compounds in sediments and by 2,3-ring compounds in SPM samples. Assessment of PAH sources suggested that biomass and coal combustion is the major PAH source to the outer part of the estuary sediments and that petroleum combustion is the major PAH source to the inner part of estuary sediments. As for SPM samples, PAH isomer pair ratios indicated multiple (petroleum, petroleum combustion, and biomass and coal combustion) PAH sources, and significant temporal variations could exist for the sources of water column PAHs in the study area. The distribution of perylene in SPM samples indicated that the river was the dominant source of perylene in SPM and that perylene could be taken as an index to assess the contribution of river inflow to the total PAHs in SPM samples. The high concentration of perylene in the sediment was indicative of an in situ biogenic origin. - PAH were determined in suspended particulate matter and sediments from Pearl River Estuary

Submicron particulate organic matter in the urban atmosphere: a new method for real-time measurement, molecular-level characterization and source apportionment

Science.gov (United States)

Müller, Markus; Eichler, Philipp; D'Anna, Barbara; Tan, Wen; Wisthaler, Armin

2017-04-01

We used a novel chemical analytical method for measuring submicron particulate organic matter in the atmosphere of three European cities (Innsbruck, Lyon, Valencia). Proton-Transfer-Reaction Time-of-Flight Mass Spectrometry (PTR-ToF-MS) was used in combination with the "chemical analysis of aerosol online" (CHARON) inlet for detecting particulate organic compounds on-line (i.e. without filter pre-collection), in real-time (1-min time resolution), at ng m-3 concentrations, with molecular-level resolution (i.e. obtaining molecular weight and elemental composition information). The CHARON-PTR-ToF-MS system monitored molecular tracers associated with different particle sources including levoglucosan from biomass combustion, PAHs from vehicular traffic, nicotine from cigarette smoking, and monoterpene oxidation products secondarily formed from biogenic emissions. The tracer information was used for interpreting positive matrix factorization (PMF) data which allowed us to apportion the sources of submicron particulate organic matter in the different urban environments. This work was funded through the PIMMS ITN, which was supported by the European Commission's 7th Framework Programme under grant agreement number 287382.

Method and apparatus for sampling atmospheric mercury

Science.gov (United States)

Trujillo, Patricio E.; Campbell, Evan E.; Eutsler, Bernard C.

1976-01-20

A method of simultaneously sampling particulate mercury, organic mercurial vapors, and metallic mercury vapor in the working and occupational environment and determining the amount of mercury derived from each such source in the sampled air. A known volume of air is passed through a sampling tube containing a filter for particulate mercury collection, a first adsorber for the selective adsorption of organic mercurial vapors, and a second adsorber for the adsorption of metallic mercury vapor. Carbon black molecular sieves are particularly useful as the selective adsorber for organic mercurial vapors. The amount of mercury adsorbed or collected in each section of the sampling tube is readily quantitatively determined by flameless atomic absorption spectrophotometry.

Kuwaiti oil fires—Particulate monitoring

Science.gov (United States)

Husain, Tahir; Amin, Mohamed B.

The total suspended particulate (TSP) matters using a high-volume sampler and inhalable particulate matters using PM-10 samplers were collected at various locations in the Eastern Province of Saudi Arabia during and after the Kuwaiti oil fires. The collected samples were analysed for toxic metals and oil hydrocarbon concentrations including some carcinogenic organic compounds in addition to gravimetric analysis. The concentration values of particulate matters were determined on a daily basis at Dhahran. Abqaiq, Rahima, Tanajib and Jubail locations. The analyses of the filters show a high concentration of the inhalable particulate at various locations, especially when north or northwest winds were blowing. It was found that the inhalable particulate concentration exceeded the Meteorology and Environmental Protection Administration (MEPA) permissible limit of 340 μg m- 3 at most of these locations during May-October 1991. A trend between the total suspended particulate and inhalable particulate measured concurrently at the same locations was observed and a regression equation was developed to correlate PM-10 data with the total suspended particulate data.

Sources and oxidative potential of water-soluble humic-like substances (HULISWS) in fine particulate matter (PM2.5) in Beijing

Science.gov (United States)

Ma, Yiqiu; Cheng, Yubo; Qiu, Xinghua; Cao, Gang; Fang, Yanhua; Wang, Junxia; Zhu, Tong; Yu, Jianzhen; Hu, Di

2018-04-01

Water-soluble humic-like substances (HULISWS) are a major redox-active component of ambient fine particulate matter (PM2.5); however, information on their sources and associated redox activity is limited. In this study, HULISWS mass concentration, various HULISWS species, and dithiothreitol (DTT) activity of HULISWS were quantified in PM2.5 samples collected during a 1-year period in Beijing. Strong correlation was observed between HULISWS and DTT activity; both exhibited higher levels during the heating season than during the nonheating season. Positive matrix factorization analysis of both HULISWS and DTT activity was performed. Four combustion-related sources, namely coal combustion, biomass burning, waste incineration, and vehicle exhausts, and one secondary factor were resolved. In particular, waste incineration was identified as a source of HULISWS for the first time. Biomass burning and secondary aerosol formation were the major contributors ( > 59 %) to both HULISWS and associated DTT activity throughout the year. During the nonheating season, secondary aerosol formation was the most important source, whereas during the heating season, the predominant contributor was biomass burning. The four combustion-related sources accounted for > 70 % of HULISWS and DTT activity, implying that future reduction in PM2.5 emissions from combustion activities can substantially reduce the HULISWS burden and their potential health impact in Beijing.

Collection of size fractionated particulate matter sample for neutron activation analysis in Japan

International Nuclear Information System (INIS)

Otoshi, Tsunehiko; Nakamatsu, Hiroaki; Oura, Yasuji; Ebihara, Mitsuru

2004-01-01

According to the decision of the 2001 Workshop on Utilization of Research Reactor (Neutron Activation Analysis (NAA) Section), size fractionated particulate matter collection for NAA was started from 2002 at two sites in Japan. The two monitoring sites, ''Tokyo'' and ''Sakata'', were classified into ''urban'' and ''rural''. In each site, two size fractions, namely PM 2-10 '' and PM 2 '' particles (aerodynamic particle size between 2 to 10 micrometer and less than 2 micrometer, respectively) were collected every month on polycarbonate membrane filters. Average concentrations of PM 10 (sum of PM 2-10 and PM 2 samples) during the common sampling period of August to November 2002 in each site were 0.031mg/m 3 in Tokyo, and 0.022mg/m 3 in Sakata. (author)

Airborne particulate matter in spacecraft

Science.gov (United States)

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.

Source Apportionment of Primary and Secondary Fine Particulate Matter in China

Science.gov (United States)

Hu, J.; Zhang, H.; Ying, Q.

2015-12-01

In the past few decades, China have been facing extreme particulate matter (PM) pollution problems due to the combination of fast increase of population, industrialization, urbanization and associated energy consumption and lagging of sufficient emission control measures. Studies have identified the major components of fine PM (PM2.5) in China include primary PM (which is directly emitted into the atmosphere), sulfate and nitrate (which are mainly secondary PM, i.e., formed from gaseous precursors), and organic aerosols (which can be primary or secondary). Contributions of different source sectors to the different PM components are substantially different; therefore source apportionment of these components can provide critical information needed for policy makers to design effective emission control strategies. In the current study, a source-oriented version of the Community Multiscale Air Quality (CMAQ) model that directly tracks the contributions from multiple emission sources to primary and secondary PM2.5 is developed, and then applied to determine the regional contributions of power, industry, transportation and residential sectors to primary PM, nitrate and sulfate concentrations in China. Four months in 2012-2013 are simulated to predict the seasonal variations of source contributions. Model predictions are evaluated with ambient measured concentrations. The source-oriented CMAQ model is capable of reproducing most of the available PM10 and PM2.5 mass, and PM2.5 EC, POC, nitrate and sulfate observations. Predicted source contributions for EC also generally agree with to the source contributions estimated by receptor models reported in previous studies. Model predictions suggest residential is a major contributor to primary PM (30-70%) in the spring and winter, and industrial contributes 40-60% of primary PM in the summer and fall; Transportation is an important source for EC (20-30%); Power sector is the dominating source of nitrate and sulfate in both

An assessment of common atmospheric particulate matter sampling ...

African Journals Online (AJOL)

The method detection limit was also low (0.2 to 1 μg/L) for most metals, and 50% and less standard deviation to mean ratios were obtained for Ni and Pb. Key words: Toxic metals, inductively coupled plasma mass spectroscopy, scanning electron microscopy coupled with energy dispersive spectrometry, particulate matter, ...

Temporal variations of fine and coarse particulate matter sources in Jeddah, Saudi Arabia.

Science.gov (United States)

Lim, Chris C; Thurston, George D; Shamy, Magdy; Alghamdi, Mansour; Khoder, Mamdouh; Mohorjy, Abdullah M; Alkhalaf, Abdulrahman K; Brocato, Jason; Chen, Lung Chi; Costa, Max

2018-02-01

This study provides the first comprehensive analysis of the seasonal variations and weekday/weekend differences in fine (aerodynamic diameter Saudi Arabia. Air quality samples were collected over 1 yr, from June 2011 to May 2012 at a frequency of three times per week, and analyzed. The average mass concentrations of PM 2.5 (21.9 μg/m 3 ) and PM 10 (107.8 μg/m 3 ) during the sampling period exceeded the recommended annual average levels by the World Health Organization (WHO) for PM 2.5 (10 μg/m 3 ) and PM 10 (20 μg/m 3 ), respectively. Similar to other Middle Eastern locales, PM 2.5-10 is the prevailing mass component of atmospheric particulate matter at Jeddah, accounting for approximately 80% of the PM 10 mass. Considerations of enrichment factors, absolute principal component analysis (APCA), concentration roses, and backward trajectories identified the following source categories for both PM 2.5 and PM 2.5-10 : (1) soil/road dust, (2) incineration, and (3) traffic; and for PM 2.5 only, (4) residual oil burning. Soil/road dust accounted for a major portion of both the PM 2.5 (27%) and PM 2.5-10 (77%) mass, and the largest source contributor for PM 2.5 was from residual oil burning (63%). Temporal variations of PM 2.5-10 and PM 2.5 were observed, with the elevated concentration levels observed for mass during the spring (due to increased dust storm frequency) and on weekdays (due to increased traffic). The predominant role of windblown soil and road dust in both the PM 2.5 and PM 2.5-10 masses in this city may have implications regarding the toxicity of these particles versus those in the Western world where most PM health assessments have been made in the past. These results support the need for region-specific epidemiological investigations to be conducted and considered in future PM standard setting. Temporal variations of fine and coarse PM mass, elemental constituents, and sources were examined in Jeddah, Saudi Arabia, for the first time. The main source

Monitoring diesel particulate matter and calculating diesel particulate densities using Grimm model 1.109 real-time aerosol monitors in underground mines.

Science.gov (United States)

Kimbal, Kyle C; Pahler, Leon; Larson, Rodney; VanDerslice, Jim

2012-01-01

Currently, there is no Mine Safety and Health Administration (MSHA)-approved sampling method that provides real-time results for ambient concentrations of diesel particulates. This study investigated whether a commercially available aerosol spectrometer, the Grimm Portable Aerosol Spectrometer Model 1.109, could be used during underground mine operations to provide accurate real-time diesel particulate data relative to MSHA-approved cassette-based sampling methods. A subset was to estimate size-specific diesel particle densities to potentially improve the diesel particulate concentration estimates using the aerosol monitor. Concurrent sampling was conducted during underground metal mine operations using six duplicate diesel particulate cassettes, according to the MSHA-approved method, and two identical Grimm Model 1.109 instruments. Linear regression was used to develop adjustment factors relating the Grimm results to the average of the cassette results. Statistical models using the Grimm data produced predicted diesel particulate concentrations that highly correlated with the time-weighted average cassette results (R(2) = 0.86, 0.88). Size-specific diesel particulate densities were not constant over the range of particle diameters observed. The variance of the calculated diesel particulate densities by particle diameter size supports the current understanding that diesel emissions are a mixture of particulate aerosols and a complex host of gases and vapors not limited to elemental and organic carbon. Finally, diesel particulate concentrations measured by the Grimm Model 1.109 can be adjusted to provide sufficiently accurate real-time air monitoring data for an underground mining environment.

Ferruginous compounds in the airborne particulate matter of the metropolitan area of Belo Horizonte, Minas Gerais, Brazil.

Science.gov (United States)

Tavares, Fernanda Vasconcelos Fonseca; Ardisson, José Domingos; Rodrigues, Paulo César Horta; Fabris, José Domingos; Fernandez-Outon, Luis Eugenio; Feliciano, Vanusa Maria Delage

2017-08-01

Samples of soil, iron ore, and airborne particulate matter (size airborne particulate matter in the metropolitan area of Belo Horizonte, Minas Gerais, Brazil, are either from natural origin, as, for instance, re-suspension of particles from soil, or due to anthropogenic activities, meaning that it would be originated from the many iron ore minings surrounding the metropolitan area. Numerical simulations were used to model the atmospheric dispersion of the airborne particulate matter emitted by iron mining located at the Iron Quadrangle geodomain, Minas Gerais. Results from these numerical simulations supported identifying the sites with the highest concentrations of airborne particulate matter in the metropolitan area. Samples of these suspended materials were collected at the selected sites by using high-volume air samplers. The physicochemical features of the solid materials were assessed by X-ray fluorescence, X-ray diffraction, magnetometry, and 57 Fe Mössbauer spectroscopy. The soil materials were found to be rich in quartz, aluminum, organic matter, and low contents of iron, mainly as low crystalline iron oxides. The samples of the iron ores, on the other hand, contain high concentration of iron, dominantly as relatively pure and crystalline hematite (α-Fe 2 O 3 ). The samples of the airborne particulate matter are rich in iron, mainly as hematite, but contained also quartz, aluminum, and calcium. Mössbauer spectroscopy was used to evaluate the hyperfine structure of 57 Fe of the hematite both from the iron ore and the soil samples. The structural characteristics of the hematite of these particulate materials were further explored. The direct influence of the iron ore mining on the composition of the airborne particulate matter was clearly evidenced based on the trace ability of hematite to its source of emission. Even the atmospheric air on regions relatively far away from the mining activities is also significantly influenced.

Heavy metal analysis of suspended particulate matter (SPM) and other samples from some workplaces in Kenya

International Nuclear Information System (INIS)

Kinyua, A.M.; Gatebe, C.K.; Mangala, M.J.

1998-01-01

Air pollution studies in Nairobi are indicating a rising trend in the particulate matter loading. The trend is mainly attributed to increased volume of motor vehicles, the physical change of the environment, agricultural and industrial activities. In this study, total suspended particulate matter sampling at the Nairobi industrial area and inside one workplace are reported. Included also are the results of analysis of water samples and effluents collected from a sugar factory, a tannery, and mercury (Hg) analysis in some beauty creams sold in Nairobi. The samples were analysed for heavy metal content using Energy Dispersive X-ray Fluorescence (EDXRF) while the suspended particulate matter (SPM) concentrations were determined by gravimetric technique. Total reflection x-ray fluorescence (TRXF), atomic absorption spectrophotometry and PIXE analytical techniques plus the use of Standard and Certified Reference Materials (SRM's and CRM's) were used for quality control, analysis and evaluation of the accrued data. Air sampling in the industrial area was done twice (Wednesday and Saturday) every week for a period of two months (November and December, 1996) and twice monthly for a period of six months (January-June 1997). Each sample covering approximately 24 hours, was collected using the 'Gent' Stacked Filter Unit (SFU), for day and night times. The SPM were found to vary from 16 to 83 mgm -3 during the sampling period. The analysis of dust collected inside a workplace showed that there was poor filtration of the air pumped into the building and that there was a need for improvement of the air conditioning unit plus reduction of emissions from a neighbouring tyre factory. Beauty creams analysed showed that there is some mercury present in significant amounts (0.14 - 3.0%). The results of these mercury levels are presented for various brands of cosmetics sold in some market outlets in Nairobi. The health implications on the presence of mercury in some of these beauty

PM{sub 10} sampler deposited air particulates: Ascertaining uniformity of sample on filter through rotated exposure to radiation

Energy Technology Data Exchange (ETDEWEB)

Owoade, Oyediran K. [Environmental Research Laboratory (ERL), Physics Department, Obafemi Awolowo University, Ile-Ife (Nigeria)]. E-mail: oowoade2001@yahoo.com; Olise, Felix S. [Environmental Research Laboratory (ERL), Physics Department, Obafemi Awolowo University, Ile-Ife (Nigeria); Obioh, Imoh B. [Centre for Energy Research, Development (Cerd), Obafemi Awolowo University, Ile-Ife (Nigeria); Olaniyi, Hezekiah B. [Environmental Research Laboratory (ERL), Physics Department, Obafemi Awolowo University, Ile-Ife (Nigeria); Bolzacchini, Ezio [Universita Milano-Bicocca, Dipartimento di Scienze-Ambientali, Pizza della Scienza, Milan (Italy); Ferrero, Luca [Universita Milano-Bicocca, Dipartimento di Scienze-Ambientali, Pizza della Scienza, Milan (Italy); Perrone, Grazia [Universita Milano-Bicocca, Dipartimento di Scienze-Ambientali, Pizza della Scienza, Milan (Italy)

2006-08-01

For reproducibility of analytical results of samples deposited on filters using PM{sub 10} sampler, homogeneity of the sample on the filter is very important especially when the size of the X-ray beam for the analysis is less than the size of filter. It is against this background that the air particulate samples collected on using PM{sub 10} samplers are analysed to determine the elemental concentrations. Each sample was divided into four quadrants and each was analysed under same conditions to determine if the particles were deposited uniformly over the filter. Each analysis was done using EDXRF technique. The spectrometer consists of four secondary targets, which are automatically switched to in sequence in analysing each sample. The concentration of various elements detected was determined using TURBOQUANT (a brand name for a SPECTRO method which is used for screening analysis). Sixteen elements were detected in every sample. Results show that there was less than 10% deviation in the concentrations in different quadrants. There were a few elements like Ba, Cs, etc., which have deviation greater than 20%. The concentrations of these latter elements were close to detection limits of the spectrometer. We conclude that the analytical result of particulate samples deposited on filters by the PM{sub 10} sampler can be reliable in terms of the homogeneity of the deposition. For such analytes with low concentrations, it would be important that the sampling time be increased to allow for higher mass deposition on the filter.

SOURCE SAMPLING FINE PARTICULATE MATTER: A KRAFT PROCESS RECOVERY BOILER AT A PULP AND PAPER FACILITY, VOLUMES 1 AND 2

Science.gov (United States)

Fine particulate matter of aerodynamic diameter 2.5 m or less (PM-2.5) has been found harmful to human health, and a National Ambient Air Quality Standard for PM-2.5 was promulgated by the U.S. Environmental Protection Agency in July 1997. A national network of ambient monitorin...

Characteristic of ambient airborne and respirable particulate around a non formal industrial area

International Nuclear Information System (INIS)

Muhayatun Santoso; Diah Dwiana Lestiani; Mariana Marselina; Rita Mukhtar

2016-01-01

Characterization of airborne particulate matter and respirable particulate in Parung Panjang district especially on surrounding non formal used batteries industrial area has been carried out to follow up the previous results with respect to high concentrations of lead detected in Serpong area. Sampling of airborne particulate matter in Parung Panjang was conducted using Gent stacked filter unit sampler, while the respirable particulate matter samples collected using personal dust sampler in Parung Panjang as a non formal Industrial area and Sukarasa village as a control, during 2011-2012. The concentration of masses were determined gravimetrically, while for elemental concentrations by X-Ray based methods. The average of mass concentration of air ambient PM 2.5 and PM 10 in Parung Panjang were 27.3 ± 13.7 and 77.5 ± 17.1 μg.m -3 , respectively. While the average concentration of respirable particulate in non formal industrial and control areas were 260 ± 233 and 82 ± 38 μg.m -3 , respectively. The percentage of average Pb concentration in PM 2.5 and PM 2.5-10 were contribute up to 45 and 10 % of the mass concentration, respectively. The maximum percentage concentration of Pb in respirable particulate in industrial and control area were 12.11 and 0.27 %, respectively. These results showed that the Pb concentrations in respirable particulate in industrial area were significantly tens times higher than in the control area. The high concentration of Pb in Parung Panjang was the main key element came from the used lead battery industry and one of pollutant source that contributed to the Pb pollution in Serpong area. (author)

Temporal and spatial variations in particulate matter, particulate organic carbon and attenuation coefficient in Cochin Backwaters

Digital Repository Service at National Institute of Oceanography (India)

Devi, K.S.

Nine stations over a stretch of 21 km of Periyar river estuary were sampled during January to December 1981. Particulate matter varied from 3-253 mg.1 super(1) at the surface and 24.8-257mg.1 super(1) at the bottom. Particulate organic carbon ranged...

Complexity analysis in particulate matter measurements

Directory of Open Access Journals (Sweden)

Luciano Telesca

2011-09-01

Full Text Available We investigated the complex temporal fluctuations of particulate matter data recorded in London area by using the Fisher-Shannon (FS information plane. In the FS plane the PM10 and PM2.5 data are aggregated in two different clusters, characterized by different degrees of order and organization. This results could be related to different sources of the particulate matter.

Sources of particulate matter components in the Athabasca oil sands region: investigation through a comparison of trace element measurement methodologies

Science.gov (United States)

Phillips-Smith, Catherine; Jeong, Cheol-Heon; Healy, Robert M.; Dabek-Zlotorzynska, Ewa; Celo, Valbona; Brook, Jeffrey R.; Evans, Greg

2017-08-01

The province of Alberta, Canada, is home to three oil sands regions which, combined, contain the third largest deposit of oil in the world. Of these, the Athabasca oil sands region is the largest. As part of Environment and Climate Change Canada's program in support of the Joint Canada-Alberta Implementation Plan for Oil Sands Monitoring program, concentrations of trace elements in PM2. 5 (particulate matter smaller than 2.5 µm in diameter) were measured through two campaigns that involved different methodologies: a long-term filter campaign and a short-term intensive campaign. In the long-term campaign, 24 h filter samples were collected once every 6 days over a 2-year period (December 2010-November 2012) at three air monitoring stations in the regional municipality of Wood Buffalo. For the intensive campaign (August 2013), hourly measurements were made with an online instrument at one air monitoring station; daily filter samples were also collected. The hourly and 24 h filter data were analyzed individually using positive matrix factorization. Seven emission sources of PM2. 5 trace elements were thereby identified: two types of upgrader emissions, soil, haul road dust, biomass burning, and two sources of mixed origin. The upgrader emissions, soil, and haul road dust sources were identified through both the methodologies and both methodologies identified a mixed source, but these exhibited more differences than similarities. The second upgrader emissions and biomass burning sources were only resolved by the hourly and filter methodologies, respectively. The similarity of the receptor modeling results from the two methodologies provided reassurance as to the identity of the sources. Overall, much of the PM2. 5-related trace elements were found to be anthropogenic, or at least to be aerosolized through anthropogenic activities. These emissions may in part explain the previously reported higher levels of trace elements in snow, water, and biota samples collected

Sources of particulate matter components in the Athabasca oil sands region: investigation through a comparison of trace element measurement methodologies

Directory of Open Access Journals (Sweden)

C. Phillips-Smith

2017-08-01

Full Text Available The province of Alberta, Canada, is home to three oil sands regions which, combined, contain the third largest deposit of oil in the world. Of these, the Athabasca oil sands region is the largest. As part of Environment and Climate Change Canada's program in support of the Joint Canada-Alberta Implementation Plan for Oil Sands Monitoring program, concentrations of trace elements in PM2. 5 (particulate matter smaller than 2.5 µm in diameter were measured through two campaigns that involved different methodologies: a long-term filter campaign and a short-term intensive campaign. In the long-term campaign, 24 h filter samples were collected once every 6 days over a 2-year period (December 2010–November 2012 at three air monitoring stations in the regional municipality of Wood Buffalo. For the intensive campaign (August 2013, hourly measurements were made with an online instrument at one air monitoring station; daily filter samples were also collected. The hourly and 24 h filter data were analyzed individually using positive matrix factorization. Seven emission sources of PM2. 5 trace elements were thereby identified: two types of upgrader emissions, soil, haul road dust, biomass burning, and two sources of mixed origin. The upgrader emissions, soil, and haul road dust sources were identified through both the methodologies and both methodologies identified a mixed source, but these exhibited more differences than similarities. The second upgrader emissions and biomass burning sources were only resolved by the hourly and filter methodologies, respectively. The similarity of the receptor modeling results from the two methodologies provided reassurance as to the identity of the sources. Overall, much of the PM2. 5-related trace elements were found to be anthropogenic, or at least to be aerosolized through anthropogenic activities. These emissions may in part explain the previously reported higher levels of trace elements in snow

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

Science.gov (United States)

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.

Apportionment of the sources of high fine particulate matter concentration events in a developing aerotropolis in Taoyuan, Taiwan.

Science.gov (United States)

Chuang, Ming-Tung; Chen, Yu-Chieh; Lee, Chung-Te; Cheng, Chung-Hao; Tsai, Yu-Jen; Chang, Shih-Yu; Su, Zhen-Sen

2016-07-01

To investigate the characteristics and contributions of the sources of fine particulate matter with a size of up to 2.5 μm (PM2.5) during the period when pollution events could easily occur in Taoyuan aerotropolis, Taiwan, this study conducted sampling at three-day intervals from September 2014 to January 2015. Based on the mass concentration of PM2.5, the sampling days were classified into high PM2.5 concentration event days (PM2.5>35 μg m(-3)) and non-event days (PM2.5<35 μg m(-3)). In addition, the chemical species, including water-soluble inorganic ions, carbonaceous components, and metal elements, were analyzed. The sources of pollution and their contributions were estimated using the positive matrix factorization (PMF) model. Furthermore, the effect of the weather type on the measurement results was also explored based on wind field conditions. The mass fractions of Cl(-) and NO3(-) increased when a high PM2.5 concentration event occurred, and they were also higher under local emitted conditions than under long range transported conditions, indicating that secondary nitrate aerosols were the major increasing local species that caused high PM2.5 concentration events. Seven sources of pollution could be distinguished using the PMF model on the basis of the characteristics of the species. Industrial emissions, coal combustion/urban waste incineration, and local emissions from diesel/gasoline vehicles were the main sources that contributed to pollution on high PM2.5 concentration event days. In order to reduction of high PM2.5 concentration events, the control of diesel and gasoline vehicle emission is important and should be given priority. Copyright © 2016 Elsevier Ltd. All rights reserved.

Sources and oxidative potential of water-soluble humic-like substances (HULISWS in fine particulate matter (PM2.5 in Beijing

Directory of Open Access Journals (Sweden)

Y. Ma

2018-04-01

Full Text Available Water-soluble humic-like substances (HULISWS are a major redox-active component of ambient fine particulate matter (PM2.5; however, information on their sources and associated redox activity is limited. In this study, HULISWS mass concentration, various HULISWS species, and dithiothreitol (DTT activity of HULISWS were quantified in PM2.5 samples collected during a 1-year period in Beijing. Strong correlation was observed between HULISWS and DTT activity; both exhibited higher levels during the heating season than during the nonheating season. Positive matrix factorization analysis of both HULISWS and DTT activity was performed. Four combustion-related sources, namely coal combustion, biomass burning, waste incineration, and vehicle exhausts, and one secondary factor were resolved. In particular, waste incineration was identified as a source of HULISWS for the first time. Biomass burning and secondary aerosol formation were the major contributors ( >  59 % to both HULISWS and associated DTT activity throughout the year. During the nonheating season, secondary aerosol formation was the most important source, whereas during the heating season, the predominant contributor was biomass burning. The four combustion-related sources accounted for  >  70 % of HULISWS and DTT activity, implying that future reduction in PM2.5 emissions from combustion activities can substantially reduce the HULISWS burden and their potential health impact in Beijing.

Determination of stable isotope ratio of lead in airborne particulate matter by ICP-MS

International Nuclear Information System (INIS)

Mukai, Hitoshi; Ambe, Yoshinari

1990-01-01

ICP-MS was applied to the measurement of stable isotope ratios of lead, which are used as an indicator of the source of lead in airborne particulate matter. For the measurement of lead isotopes ratios, the influences of machine conditions, lead concentration and matrix elements to the precision and accuracy of the measurements were studied. At a scanning mode, dwell time of 40∼160 μs gave the best precision to the isotope ratio measurements; about 0.3 % of R.S.D. for 206 Pb/ 207 Pb and 206 Pb/ 208 Pb, 0.6 % for 206 Pb/ 204 Pb. Precision of the measurement was better at a high concentration of lead in sample solution. The observed value of 206 Pb/ 207 Pb ratio was not affected by the lead concentration, but in the cases of 206 Pb/ 204 Pb and 206 Pb/ 208 Pb, about 1 % of the value changed in the observed ratios with the lead concentration of 100∼500 μg/l. Six matrix elements (Na, K, Ca, Mg, Al, Fe) did not affect the observed isotope ratios up to 200 mg/l. The lead isotope ratios of reference materials {Urban Particulates (NIST) and Vehicle Exhausted Particulates (NIES)} were measured by using two kinds of sample; crude sample and lead-isolated sample from matrix elements by anodic deposition. Both cases gave the same isotope ratio values, therefore, lead isotope ratios in airborne particulate samples can be measured by ICP-MS without any separation of lead from matrix elements. (author)

Lessons learned from a review of post-accident sampling systems, high range effluent monitors and high concentration particulate iodine samplers

International Nuclear Information System (INIS)

Hull, A.P.; Knox, W.H.; White, J.R.

1987-01-01

Post-accident sampling systems (PASS), high range gaseous effluent monitors and sampling systems for particulates and iodine in high concentrations have been reviewed at twenty-one licensee sites in Region I of the US Nuclear Regulatory Commission which includes fifteen BWR's and fourteen PWR's. Although most of the installed PASS met the criteria, the highest operational readiness was found in on-line systems that were also used for routine sampling and analysis. The detectors used in the gaseous effluent monitors included external ion chambers, GM tubes, organic scintillators and Cd-Te solid state crystals. Although all were found acceptable, each had its own inherent limitations in the conversion of detector output to the time varying concentration of a post-accident mixture of noble gases. None of the installed particulate and iodine samplers fully met all of the criteria. Their principal limitations included a lack of documentation showing that they could obtain a representative sample and that many of them would collect of an excessive amount of activity at the design criteria. 10 refs., 4 figs., 5 tabs

Quantifying the sources of ozone, fine particulate matter, and regional haze in the Southeastern United States.

Science.gov (United States)

Odman, M Talat; Hu, Yongtao; Russell, Armistead G; Hanedar, Asude; Boylan, James W; Brewer, Patricia F

2009-07-01

A detailed sensitivity analysis was conducted to quantify the contributions of various emission sources to ozone (O3), fine particulate matter (PM2.5), and regional haze in the Southeastern United States. O3 and particulate matter (PM) levels were estimated using the Community Multiscale Air Quality (CMAQ) modeling system and light extinction values were calculated from modeled PM concentrations. First, the base case was established using the emission projections for the year 2009. Then, in each model run, SO2, primary carbon (PC), NH3, NO(x) or VOC emissions from a particular source category in a certain geographic area were reduced by 30% and the responses were determined by calculating the difference between the results of the reduced emission case and the base case. The sensitivity of summertime O3 to VOC emissions is small in the Southeast and ground-level NO(x) controls are generally more beneficial than elevated NO(x) controls (per unit mass of emissions reduced). SO2 emission reduction is the most beneficial control strategy in reducing summertime PM2.5 levels and improving visibility in the Southeast and electric generating utilities are the single largest source of SO2. Controlling PC emissions can be very effective locally, especially in winter. Reducing NH3 emissions is an effective strategy to reduce wintertime ammonium nitrate (NO3NH4) levels and improve visibility; NO(x) emissions reductions are not as effective. The results presented here will help the development of specific emission control strategies for future attainment of the National Ambient Air Quality Standards in the region.

Size distribution and sources of humic-like substances in particulate matter at an urban site during winter.

Science.gov (United States)

Park, Seungshik; Son, Se-Chang

2016-01-01

This study investigates the size distribution and possible sources of humic-like substances (HULIS) in ambient aerosol particles collected at an urban site in Gwangju, Korea during the winter of 2015. A total of 10 sets of size-segregated aerosol samples were collected using a 10-stage Micro-Orifice Uniform Deposit Impactor (MOUDI), and the samples were analyzed to determine the mass as well as the presence of ionic species (Na(+), NH4(+), K(+), Ca(2+), Mg(2+), Cl(-), NO3(-), and SO4(2-)), water-soluble organic carbon (WSOC) and HULIS. The separation and quantification of the size-resolved HULIS components from the MOUDI samples was accomplished using a Hydrophilic-Lipophilic Balanced (HLB) solid phase extraction method and a total organic carbon analyzer, respectively. The entire sampling period was divided into two periods: non-Asian dust (NAD) and Asian dust (AD) periods. The contributions of water-soluble organic mass (WSOM = 1.9 × WSOC) and HULIS (=1.9 × HULIS-C) to fine particles (PM1.8) were approximately two times higher in the NAD samples (23.2 and 8.0%) than in the AD samples (12.8 and 4.2%). However, the HULIS-C/WSOC ratio in PM1.8 showed little difference between the NAD (0.35 ± 0.07) and AD (0.35 ± 0.05) samples. The HULIS exhibited a uni-modal size distribution (@0.55 μm) during NAD and a bimodal distribution (@0.32 and 1.8 μm) during AD, which was quite similar to the mass size distributions of particulate matter, WSOC, NO3(-), SO4(2-), and NH4(+) in both the NAD and AD samples. The size distribution characteristics and the results of the correlation analyses indicate that the sources of HULIS varied according to the particle size. In the fine mode (≤1.8 μm), the HULIS composition during the NAD period was strongly associated with secondary organic aerosol (SOA) formation processes similar to those of secondary ionic species (cloud processing and/or heterogeneous reactions) and primary emissions during the biomass burning period, and during

Modelling airborne dispersion of coarse particulate material

International Nuclear Information System (INIS)

Apsley, D.D.

1989-03-01

Methods of modelling the airborne dispersion and deposition of coarse particulates are presented, with the emphasis on the heavy particles identified as possible constituents of releases from damaged AGR fuel. The first part of this report establishes the physical characteristics of the irradiated particulate in airborne emissions from AGR stations. The second part is less specific and describes procedures for extending current dispersion/deposition models to incorporate a coarse particulate component: the adjustment to plume spread parameters, dispersion from elevated sources and dispersion in conjunction with building effects and plume rise. (author)

Use of historical uranium air sampling data to estimate worker exposure potential to airborne radioactive particulate in a uranium processing facility.

Science.gov (United States)

Methner, M M; Feng, H A; Utterback, D F

2001-12-01

Historical industrial hygiene monitoring records from a uranium processing plant were collected and analyzed to characterize exposure potential to airborne radioactive particulate. More than 2,100 samples were collected during the period of 1954-1968. The data was organized by job title, plant number, and year of measurement. Laboratory analysis of air samples indicated a wide range of potential exposures to the alpha-emitting particulate. Logarithmic transformation of the data was necessary to approximate Gaussian distributions. Geometric Mean (GM) values were used as the measure of central tendency within years. GM values ranged from 23-49 disintegrations per minute per cubic meter of air sampled (dpm/m3) with the years 1963 and 1964 being significantly higher than other years (ANOVA: p exposure potential across plants, GM ranged from 20-68 dpm/m3, with plants 5 and 8 being significantly higher than the others (ANOVA: p Exposure potential for specific job titles across the plants varied widely. GM for clerks was the lowest (11 dpm/m3) while furnace operators were the highest (235 dpm/m3). Other job titles with potentially high exposures were chemical operators, forklift operators, machine operators, and furnace operators. This analysis indicates the magnitude and distributions of worker exposure to alpha-emitting airborne particulate. Additional analysis and epidemiologic studies are planned for this facility.

Electron spin resonance of particulate soot samples from automobiles to help environmental studies

International Nuclear Information System (INIS)

Yamanaka, C.; Matsuda, T.; Ikeya, M.

2005-01-01

The application of electron spin resonance (ESR) was studied for diesel soot samples and suspended particulate matter (SPM) from automobile engines. Soot samples or diesel exhaust particles (DEP) were recovered at various points: in the exhaust pipe of a diesel engine, at the dust sampler of a highway tunnel (standard DEP), on the soundproofing wall alongside a heavy traffic road, and on the filters of a dust sampler for SPM. The diesel soot samples apparently showed two ESR spectra: one was a broad spectrum at g=2.1 with a line width of ca. 80-120mT and the other was a sharp signal of a carbon radical at g=2.003 with a line width of 0.4mT. Annealing experiments with a DEP sample at 250 deg. C revealed drastic enhancement of the sharp ESR signal, which suggested a thermal process of carbonization of remnant organics. An oximetric study by ESR showed an enhancement of the broad signal in the diesel soot sample as well as in the sharp ESR signal. Therefore, the main part of the broad ESR signal would be attributed to carbon radicals, which form a different configuration, probably closely interacting aggregates. Enhancement of the sharp ESR signal was not observed in the standard DEP sample under vacuum condition, which suggested less adsorption sites on the surface of DEP samples

Elemental quantification of airborne particulate matter in Bandung and Lembang area

International Nuclear Information System (INIS)

Sutisna; Achmad Hidayat; Dadang Supriatna

2004-01-01

ELEMENTAL QUANTIFICATION OF AIRBORNE PARTICULATE MATTER IN BANDUNG AND LEMBANG REGION: The contaminated airborne particulates by toxic gases and elements have a potential affect to the human health. Some toxic elements related to air pollution have carcinogenic affect. The quantification of those elements is important to monitor a level of pollutant contained in the airborne particulate. The aim of this work is to analyze the air particulate sample using instrumental neutron activation analysis and other related technique. Two sampling points of Bandung and Lembang that represent and urban and rural area respectively have been chosen to collect the air particulate sample. The samplings were carried out using Gent Stacked Filter Unit Sampler for 24 hours, and two cellulose filters of 8 μm and 0.45 μm pore size were used. Trace elements in the sample collected were determined using NAA based on a comparative method. Elemental distribution on PM 2.5 and PM 10 fraction of airborne particulate was analyzed, the enrichment factor was calculated using Al as reference elements, and the black carbons contents were determined using FEL Smoke Stain Reflectometer analyzed. The results are presented and discussed. (author)

SOURCE SAMPLING FINE PARTICULATE MATTER: A KRAFT PROCESS HOGGED FUEL BOILER AT A PULP AND PAPER FACILITY, VOLUMES 1 AND 2

Science.gov (United States)

Fine particulate matter of aerodynamic diameter 2.5 m or less (PM-2.5) has been found harmful to human health, and a National Ambient Air Quality Standard for PM-2.5 was promulgated by the U.S. Environmental Protection Agency in July 1997. A national network of ambient monitorin...

Radiocarbon Analysis to Calculate New End-Member Values for Biomass Burning Source Samples Specific to the Bay Area

Science.gov (United States)

Yoon, S.; Kirchstetter, T.; Fairley, D.; Sheesley, R. J.; Tang, X.

2017-12-01

Elemental carbon (EC), also known as black carbon or soot, is an important particulate air pollutant that contributes to climate forcing through absorption of solar radiation and to adverse human health impacts through inhalation. Both fossil fuel combustion and biomass burning, via residential firewood burning, agricultural burning, wild fires, and controlled burns, are significant sources of EC. Our ability to successfully control ambient EC concentrations requires understanding the contribution of these different emission sources. Radiocarbon (14C) analysis has been increasingly used as an apportionment tool to distinguish between EC from fossil fuel and biomass combustion sources. However, there are uncertainties associated with this method including: 1) uncertainty associated with the isolation of EC to be used for radiocarbon analysis (e.g., inclusion of organic carbon, blank contamination, recovery of EC, etc.) 2) uncertainty associated with the radiocarbon signature of the end member. The objective of this research project is to utilize laboratory experiments to evaluate some of these uncertainties, particularly for EC sources that significantly impact the San Francisco Bay Area. Source samples of EC only and a mix of EC and organic carbon (OC) were produced for this study to represent known emission sources and to approximate the mixing of EC and OC that would be present in the atmosphere. These samples include a combination of methane flame soot, various wood smoke samples (i.e. cedar, oak, sugar pine, pine at various ages, etc.), meat cooking, and smoldering cellulose smoke. EC fractions were isolated using a Sunset Laboratory's thermal optical transmittance carbon analyzer. For 14C analysis, samples were sent to Woods Hole Oceanographic Institution for isotope analysis using an accelerated mass spectrometry. End member values and uncertainties for the EC isolation utilizing this method will be reported.

Peatland use and transport of particulate organic matter in boreal headwater catchments

Science.gov (United States)

Marttila, Hannu; Karjalainen, Satu-Maaria; Nieminen, Mika; Kløve, Bjørn

2014-05-01

Peatland use can cause increased transport of particulate organic matter (POM) causing deteriorated water quality and especially siltation of stream beds. Even though topic has gained major attention among stakeholders it has received only minor efforts to solve the main sources and properties of transported particles. The development of effective management practices and evaluation of purification efficiency demands understanding of the sources of particulate matter in peat dominated catchments with various land uses and hydrological conditions. The objectives of this study were: (1) to determinate physical properties of POM in headwater brooks affected by different peatland uses, and; (2) to identity the sources of transported material by using sediment fingerprinting methods. For this purpose, two headwater catchments under peat extraction and peatland forestry land uses with 8 sampling points were monitored for 2 years using time integrated suspended sediment samplers. Data was completed by gap samples from 50 other headwater locations with different upstream land uses: pristine, peatland forestry and peat extraction. For the sources analysis, disturbed topsoil, stream bed sediment, banks of ditches and brooks, algae and various vegetation types were identified as the potential sediment sources. Stable isotopes (δ13C, δ15N) and C/N ratio were analyzed to discriminate between the possible sources. Results are further scaled against different land uses, landscape elements and seasonal hydrological conditions in headwaters. This paper presents the preliminary results from a two year study aiming to show various patterns in transport of POM in boreal headwater catchments. Due to strong land-water relationship in headwaters, further information on the properties of particles is needed to assess the downstream impacts of land use.

Apportionment of the sources of high fine particulate matter concentration events in a developing aerotropolis in Taoyuan, Taiwan

International Nuclear Information System (INIS)

Chuang, Ming-Tung; Chen, Yu-Chieh; Lee, Chung-Te; Cheng, Chung-Hao; Tsai, Yu-Jen; Chang, Shih-Yu; Su, Zhen-Sen

2016-01-01

To investigate the characteristics and contributions of the sources of fine particulate matter with a size of up to 2.5 μm (PM 2.5 ) during the period when pollution events could easily occur in Taoyuan aerotropolis, Taiwan, this study conducted sampling at three-day intervals from September 2014 to January 2015. Based on the mass concentration of PM 2.5 , the sampling days were classified into high PM 2.5 concentration event days (PM 2.5 >35 μg m −3 ) and non-event days (PM 2.5 <35 μg m −3 ). In addition, the chemical species, including water-soluble inorganic ions, carbonaceous components, and metal elements, were analyzed. The sources of pollution and their contributions were estimated using the positive matrix factorization (PMF) model. Furthermore, the effect of the weather type on the measurement results was also explored based on wind field conditions. The mass fractions of Cl − and NO 3 − increased when a high PM 2.5 concentration event occurred, and they were also higher under local emitted conditions than under long range transported conditions, indicating that secondary nitrate aerosols were the major increasing local species that caused high PM 2.5 concentration events. Seven sources of pollution could be distinguished using the PMF model on the basis of the characteristics of the species. Industrial emissions, coal combustion/urban waste incineration, and local emissions from diesel/gasoline vehicles were the main sources that contributed to pollution on high PM 2.5 concentration event days. In order to reduction of high PM 2.5 concentration events, the control of diesel and gasoline vehicle emission is important and should be given priority. - Highlights: • The mass fractions of NH 4 + , K + , Cl − and NO 3 − increased during PM 2.5 event days. • Reduction of coal combustion/urban waste incineration emissions should be prioritized. • The control of vehicle emission is important in the locally emitted periods. • Secondary

Particulate carbohydrates in the Bay of Bengal

Digital Repository Service at National Institute of Oceanography (India)

Bhosle, N.B.; Nandakumar, K.; Venkat, K.

Particulate matter collected from 77 water samples over a 3000 m water column was analyzed for particulate carbohydrates (PCHO). PCHO in the surface waters ranged from 43 to 143 mu g.l-1, and below 250 m it was 16.PCHO showed large variations at all...

SOURCE SIGNATURES OF FINE PARTICULATE MATTER FROM PETROLEUM REFINING AND FUEL USE

Energy Technology Data Exchange (ETDEWEB)

Gerald P. Huffman; Frank E. Huggins; Naresh Shah; Artur Braun; Yuanzhi Chen; J. David Robertson; Joseph Kyger; Adel F. Sarofim; Ronald J. Pugmire; Henk L.C. Meuzelaar; JoAnn Lighty

2003-07-31

The molecular structure and microstructure of a suite of fine particulate matter (PM) samples produced by the combustion of residual fuel oil and diesel fuel were investigated by an array of analytical techniques. Some of the more important results are summarized below. Diesel PM (DPM): A small diesel engine test facility was used to generate a suite of diesel PM samples from different fuels under engine load and idle conditions. C XANES, {sup 13}C NMR, XRD, and TGA were in accord that the samples produced under engine load conditions contained more graphitic material than those produced under idle conditions, which contained a larger amount of unburned diesel fuel and lubricating oil. The difference was enhanced by the addition of 5% of oxygenated compounds to the reference fuel. Scanning transmission x-ray micro-spectroscopy (STXM) was able to distinguish particulate regions rich in C=C bonds from regions rich in C-H bonds with a resolution of {approx}50 nm. The former are representative of more graphitic regions and the latter of regions rich in unburned fuel and oil. The dominant microstructure observed by SEM and TEM consisted of complex chain-like structures of PM globules {approx}20-100 nm in mean diameter, with a high fractal dimension. High resolution TEM revealed that the graphitic part of the diesel soot consisted of onion-like structures made up of graphene layers. Typically 3-10 graphene layers make up the ''onion rings'', with the layer spacing decreasing as the number of layers increases. ROFA PM: Residual oil fly ash (ROFA) PM has been analyzed by a new approach that combines XAFS spectroscopy with selective leaching procedures. ROFA PM{sub 2.5} and PM{sub 2.5+} produced in combustion facilities at the U.S. EPA National Risk Management Research Laboratory (NRML) were analyzed by XAFS before and after leaching with water, acid (1N HCl), and pentane. Both water and acid leaching removed most of the metal sulfates, which were the

40 CFR 86.1343-88 - Calculations; particulate exhaust emissions.

Science.gov (United States)

2010-07-01

... determined from the following equation: er31au93.070 (1) Pmass = Mass of particulate emitted per test phase... (cubic meters) per revolution. This volume is dependent on the pressure differential across the positive... be applied before Vsf is determined. (4) Pf = Mass of particulate on the sample filter (or sample and...

Nitrogen and Triple Oxygen Isotopic Analyses of Atmospheric Particulate Nitrate over the Pacific Ocean

Science.gov (United States)

Kamezaki, Kazuki; Hattori, Shohei; Iwamoto, Yoko; Ishino, Sakiko; Furutani, Hiroshi; Miki, Yusuke; Miura, Kazuhiko; Uematsu, Mitsuo; Yoshida, Naohiro

2017-04-01

Nitrate plays a significant role in the biogeochemical cycle. Atmospheric nitrate (NO3- and HNO3) are produced by reaction precursor as NOx (NO and NO2) emitted by combustion, biomass burning, lightning, and soil emission, with atmospheric oxidants like ozone (O3), hydroxyl radical (OH), peroxy radical and halogen oxides. Recently, industrial activity lead to increases in the concentrations of nitrogen species (NOx and NHy) throughout the environment. Because of the increase of the amount of atmospheric nitrogen deposition, the oceanic biogeochemical cycle are changed (Galloway et al., 2004; Kim et al., 2011). However, the sources and formation pathways of atmospheric nitrate are still uncertain over the Pacific Ocean because the long-term observation is limited. Stable isotope analysis is useful tool to gain information of sources, sinks and formation pathways. The nitrogen stable isotopic composition (δ15N) of atmospheric particulate NO3- can be used to posses information of its nitrogen sources (Elliott et al., 2007). Triple oxygen isotopic compositions (Δ17O = δ17O - 0.52 ×δ18O) of atmospheric particulate NO3- can be used as tracer of the relative importance of mass-independent oxygen bearing species (e.g. O3, BrO; Δ17O ≠ 0 ‰) and mass-dependent oxygen bearing species (e.g. OH radical; Δ17O ≈ 0 ‰) through the formation processes from NOx to NO3- in the atmosphere (Michalski et al., 2003; Thiemens, 2006). Here, we present the isotopic compositions of atmospheric particulate NO3- samples collected over the Pacific Ocean from 40˚ S to 68˚ N. We observed significantly low δ15N values for atmospheric particulate NO3- on equatorial Pacific Ocean during both cruises. Although the data is limited, combination analysis of δ15N and Δ17O values for atmospheric particulate NO3- showed the possibility of the main nitrogen source of atmospheric particulate NO3- on equatorial Pacific Ocean is ammonia oxidation in troposphere. Furthermore, the Δ17O values

Fine particulate matter in the indoor air of barbeque restaurants: Elemental compositions, sources and health risks

International Nuclear Information System (INIS)

Taner, Simge; Pekey, Beyhan; Pekey, Hakan

2013-01-01

Cooking is a significant source of indoor particulate matter that can cause adverse health effects. In this study, a 5-stage cascade impactor was used to collect particulate matter from 14 restaurants that cooked with charcoal in Kocaeli, the second largest city in Turkey. A total of 24 elements were quantified using ICP-MS. All of the element contents except for Mn were higher for fine particles (PM 2.5 ) than coarse particles (PM >2.5 ), and the major trace elements identified in the PM 2.5 included V, Se, Zn, Cr, As, Cu, Ni, and Pb. Principle component analysis (PCA) and enrichment factor (EF) calculations were used to determine the sources of PM 2.5 . Four factors that explained over 77% of the total variance were identified by the PCA. These factors included charcoal combustion, indoor activities, crustal components, and road dust. The Se, As, Cd, and V contents in the PM 2.5 were highly enriched (EF > 100). The health risks posed by the individual metals were calculated to assess the potential health risks associated with inhaling the fine particles released during charcoal cooking. The total hazard quotient (total HQ) for a PM 2.5 of 4.09 was four times greater than the acceptable limit (i.e., 1.0). In addition, the excess lifetime cancer risk (total ELCR) for PM 2.5 was 1.57 × 10 −4 , which is higher than the acceptable limit of 1.0 × 10 −6 . Among all of the carcinogenic elements present in the PM 2.5 , the cancer risks resulting from Cr(VI) and As exposure were the highest (i.e., 1.16 × 10 −4 and 3.89 × 10 −5 , respectively). Overall, these results indicate that the lifetime cancer risk associated with As and Cr(VI) exposure is significant at selected restaurants, which is of concern for restaurant workers. - Highlights: • Particulate emissions from charcoal combustion in the BBQ restaurants were studied. • Vanadium, Se, Zn, Cr and As were found as high concentrations in PM 2.5 . • Charcoal combustion and indoor activities were the

Fine particulate matter in the indoor air of barbeque restaurants: Elemental compositions, sources and health risks

Energy Technology Data Exchange (ETDEWEB)

Taner, Simge; Pekey, Beyhan, E-mail: bpekey@kocaeli.edu.tr; Pekey, Hakan

2013-06-01

Cooking is a significant source of indoor particulate matter that can cause adverse health effects. In this study, a 5-stage cascade impactor was used to collect particulate matter from 14 restaurants that cooked with charcoal in Kocaeli, the second largest city in Turkey. A total of 24 elements were quantified using ICP-MS. All of the element contents except for Mn were higher for fine particles (PM{sub 2.5}) than coarse particles (PM{sub >2.5}), and the major trace elements identified in the PM{sub 2.5} included V, Se, Zn, Cr, As, Cu, Ni, and Pb. Principle component analysis (PCA) and enrichment factor (EF) calculations were used to determine the sources of PM{sub 2.5}. Four factors that explained over 77% of the total variance were identified by the PCA. These factors included charcoal combustion, indoor activities, crustal components, and road dust. The Se, As, Cd, and V contents in the PM{sub 2.5} were highly enriched (EF > 100). The health risks posed by the individual metals were calculated to assess the potential health risks associated with inhaling the fine particles released during charcoal cooking. The total hazard quotient (total HQ) for a PM{sub 2.5} of 4.09 was four times greater than the acceptable limit (i.e., 1.0). In addition, the excess lifetime cancer risk (total ELCR) for PM{sub 2.5} was 1.57 × 10{sup −4}, which is higher than the acceptable limit of 1.0 × 10{sup −6}. Among all of the carcinogenic elements present in the PM{sub 2.5}, the cancer risks resulting from Cr(VI) and As exposure were the highest (i.e., 1.16 × 10{sup −4} and 3.89 × 10{sup −5}, respectively). Overall, these results indicate that the lifetime cancer risk associated with As and Cr(VI) exposure is significant at selected restaurants, which is of concern for restaurant workers. - Highlights: • Particulate emissions from charcoal combustion in the BBQ restaurants were studied. • Vanadium, Se, Zn, Cr and As were found as high concentrations in PM{sub 2.5}. �

Study of Hydrothermal Particulate Matter from a Shallow Venting System, offshore Nayarit, Mexico

Science.gov (United States)

Ortega-Osorio, A.; Prol-Ledesma, R. M.; Reyes, A. G.; Rubio-Ramos, M. A.; Torres-Vera, M. A.

2001-12-01

A shallow (30 ft) hydrothermal site named ``Cora'' (after the indigenous people thereby) was surveyed and sampled throughout direct observation with SCUBA diving during November 25 to December 4, 2000. A total of 10 dives were conducted in order to obtain representative samples from an 85oC fluid source of approximately 10 cm in diameter. Inherent difficulties to the sampling, such as poor visibility and strong bottom currents were overcome and samples of hydrothermal fluid, gas, rocks, and particulate matter were collected directly from the vent. Water samples and hydrothermal fluid were taken with a homemade 1 l cylindrical bottles of two lines by flushing in from the bottom for about ten minutes until total displacement of the seawater; similar procedure was carried out for gas samples. Particulate matter was collected with 0.4mm polycarbonate membrane filters and preserved in a desiccators at a fridge temperature until analysis onshore. Preliminary description of the rock samples suggest that pyritization is the main mineralisation process. Filters containing hydrothermal particulate matter were surveyed under the scanning electron microscope in order to identify the nature (inorganic and organic), as well as the chemistry of the particles. SEM examination revealed the presence of particles of different kind that suggests high degree of mixing and re-suspension: Planctonic organisms and organic matter appeared to be abundant; 25 micron particles of different carbonate faces and inorganic particles of silicates were also recognized. Distinctive euhedral colloidal grains were identified as the resulting process of precipitation from the solution. Microanalysis of iron and sulfur content of 10 micron particles indicate a very likely sulphide mineral face (greigite); 8 micron cinnabar particles are consistent with the mineralization conditions, observed as well in the inner walls of the vent. Analyses of dissolved and particulate trace metals are still ongoing at

Measurements of light absorbing particulates on the glaciers in the Cordillera Blanca, Peru

Science.gov (United States)

Schmitt, C. G.; All, J. D.; Schwarz, J. P.; Arnott, W. P.; Cole, R. J.; Lapham, E.; Celestian, A.

2014-10-01

Glaciers in the tropical Andes have been rapidly losing mass since the 1970s. In addition to the documented increase in air temperature, increases in light absorbing particulates deposited on glaciers could be contributing to the observed glacier loss. Here we report on measurements of light absorbing particulates sampled from glaciers during three surveys in the Cordillera Blanca in Peru. During three research expeditions in the dry seasons (May-August) of 2011, 2012 and 2013, two hundred and forty snow samples were collected from fifteen mountain peaks over altitudes ranging from 4800 to nearly 6800 m. Several mountains were sampled each of the three expeditions and some mountains were sampled multiple times during the same expedition. Collected snow samples were melted and filtered in the field then later analyzed using the Light Absorption Heating Method (LAHM), a new technique that measures the ability of particulates on filters to absorb visible light. LAHM results have been calibrated using filters with known amounts of fullerene soot, a common industrial surrogate for black carbon (BC). As sample filters often contain dust in addition to BC, results are presented in terms of effective Black Carbon (eBC). During the 2013 survey, snow samples were collected and kept frozen for analysis with a Single Particle Soot Photometer (SP2). Calculated eBC mass from the filter analysis and the SP2 refractory Black Carbon (rBC) results were well correlated (r2 = 0.92). These results indicate that a substantial portion of the light absorbing particulates in the more polluted areas were likely BC. The three years of data show that glaciers in the Cordillera Blanca Mountains close to human population centers have substantially higher levels of eBC (as high as 70 ng g-1) than remote glaciers (as low as 2.0 ng g-1 eBC), indicating that population centers can influence local glaciers by sourcing BC.

Estimating particulate matter health impact related to the combustion of different fossil fuels

OpenAIRE

Kuenen , Jeroen; Gschwind , Benoît; Drebszok , Kamila M.; Stetter , Daniel; Kranenburg , Richard; Hendriks , Carlijn; Lefèvre , Mireille; Blanc , Isabelle; Wyrwa , Artur; Schaap , Martijn

2013-01-01

International audience; 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. We have successfully generated a web map service that allows to access information on fuel dependent health effects due to particulate matter. For this purpose, the LOTOS-EUROS air pollution model was equipped with a source apportionment module that tracks the origin...

Role of solubles and particulates in radionuclide accumulation in the oyster Crassostrea Gigas in the discharge canal of a nuclear power plant

International Nuclear Information System (INIS)

Harrison, F.L.; Wong, K.M.; Heft, R.E.

1972-01-01

Changes in 54 Mn, 60 Co, 65 Zn, and 137 Cs concentrations were followed in oysters introduced into a discharge canal receiving low-level radioactive waste from a boiling water reactor. Groups of animals were maintained either in filtered or nonfiltered discharge-canal water. They were sampled immediately before and after single radioactive releases and at one-day intervals thereafter. Radionuclide concentrations were determined also in the water and in suspended and settled particulates. In the canal water, concentrations changed rapidly during a release, reaching peak values within 30 minutes. The partition between soluble and particulate (filterable) phases in the water differed with the radionuclide. Continuous sampling of suspended particulates after single releases showed considerable variation in concentrations per liter of water for each radionuclide. Comparisons of animals held in filtered water to those in nonfiltered water showed similar concentrations only for 137 Cs. Results indicate that suspended particulates play an important role in the accumulation of some radionuclides and that resuspension of particulates is an important source between periods of releases. (U.S.)

Relationship between Particulate matter less than 10 microns exposures and health effects on humans in Ahvaz, Iran

Directory of Open Access Journals (Sweden)

Sahar Geravandi

2015-06-01

Full Text Available Background & Aims of the Study: Particulate matters less than 10 microns can absorb into your lungs and reacting with the moisture and enter the circulatory system directly through the airways. The aim of this study is to assess Behavior PM 10 data in different seasons and Determination effects on human health in Ahvaz city during 2013. Materials & Methods: Data Particulate matters less than 10 microns were taken from Ahvaz Department of Environment and Meteorological Organization. Sampling was performed for 24 hours in 4 stations. Method of sampling and analysis were performed according to EPA guideline. Processing data include the instruction set correction of averaging, coding and filtering. Finally, health-effects of Particulate matters less than 10 exposures were calculated with impact of meteorological parameters and converted as input file to the Air Q model. Results: PM 10 concentration in winter season was maximum amount in the year 2013. According to the research findings, highest and the lowest Particulate matters less than 10 microns concentrations during 2013 had the Bureau of Meteorology “Havashenasi” and Head office of ADoE “Mohitzist”. Sum of total numbers of cardiovascular death and hospitals admission to respiratory diseases attributed to Particulate matters less than 10 microns were 923 and 2342 cases in 2013. Conclusions: Particulate matter emissions are highly regulated in most industrialized countries. Due to environmental concerns, most industries and dust storm phenomena are required to decrease in source produce particle mater and kind of dust collection system to control particulate emissions. Pollution prevention and control measures that reduce Particulate matters less than 10 microns can very useful for expected to reduce people’s exposures to Sulfur dioxide.

Inventory of primary particulates emissions; Inventaire des emissions de particules primaires

Energy Technology Data Exchange (ETDEWEB)

NONE

2001-12-01

CITEPA carried out a national inventory on particulate emissions. This report presents the results of this study for a great number of sectors and it covers a larger number of sources than the previous CITEPA inventories on particles and some other inventories carried out by International organisms (TNO, IIASA). In particular, at the present time, fugitive dust emissions for some sources are rarely taken into account in inventories because of poor knowledge and they are still the subject of researches in order to validate the emission results. (author)

Evaluation of sampling methods for toxicological testing of indoor air particulate matter.

Science.gov (United States)

Tirkkonen, Jenni; Täubel, Martin; Hirvonen, Maija-Riitta; Leppänen, Hanna; Lindsley, William G; Chen, Bean T; Hyvärinen, Anne; Huttunen, Kati

2016-09-01

There is a need for toxicity tests capable of recognizing indoor environments with compromised air quality, especially in the context of moisture damage. One of the key issues is sampling, which should both provide meaningful material for analyses and fulfill requirements imposed by practitioners using toxicity tests for health risk assessment. We aimed to evaluate different existing methods of sampling indoor particulate matter (PM) to develop a suitable sampling strategy for a toxicological assay. During three sampling campaigns in moisture-damaged and non-damaged school buildings, we evaluated one passive and three active sampling methods: the Settled Dust Box (SDB), the Button Aerosol Sampler, the Harvard Impactor and the National Institute for Occupational Safety and Health (NIOSH) Bioaerosol Cyclone Sampler. Mouse RAW264.7 macrophages were exposed to particle suspensions and cell metabolic activity (CMA), production of nitric oxide (NO) and tumor necrosis factor (TNFα) were determined after 24 h of exposure. The repeatability of the toxicological analyses was very good for all tested sampler types. Variability within the schools was found to be high especially between different classrooms in the moisture-damaged school. Passively collected settled dust and PM collected actively with the NIOSH Sampler (Stage 1) caused a clear response in exposed cells. The results suggested the higher relative immunotoxicological activity of dust from the moisture-damaged school. The NIOSH Sampler is a promising candidate for the collection of size-fractionated PM to be used in toxicity testing. The applicability of such sampling strategy in grading moisture damage severity in buildings needs to be developed further in a larger cohort of buildings.

Two Model-Based Methods for Policy Analyses of Fine Particulate Matter Control in China: Source Apportionment and Source Sensitivity

Science.gov (United States)

Li, X.; Zhang, Y.; Zheng, B.; Zhang, Q.; He, K.

2013-12-01

Anthropogenic emissions have been controlled in recent years in China to mitigate fine particulate matter (PM2.5) pollution. Recent studies show that sulfate dioxide (SO2)-only control cannot reduce total PM2.5 levels efficiently. Other species such as nitrogen oxide, ammonia, black carbon, and organic carbon may be equally important during particular seasons. Furthermore, each species is emitted from several anthropogenic sectors (e.g., industry, power plant, transportation, residential and agriculture). On the other hand, contribution of one emission sector to PM2.5 represents contributions of all species in this sector. In this work, two model-based methods are used to identify the most influential emission sectors and areas to PM2.5. The first method is the source apportionment (SA) based on the Particulate Source Apportionment Technology (PSAT) available in the Comprehensive Air Quality Model with extensions (CAMx) driven by meteorological predictions of the Weather Research and Forecast (WRF) model. The second method is the source sensitivity (SS) based on an adjoint integration technique (AIT) available in the GEOS-Chem model. The SA method attributes simulated PM2.5 concentrations to each emission group, while the SS method calculates their sensitivity to each emission group, accounting for the non-linear relationship between PM2.5 and its precursors. Despite their differences, the complementary nature of the two methods enables a complete analysis of source-receptor relationships to support emission control policies. Our objectives are to quantify the contributions of each emission group/area to PM2.5 in the receptor areas and to intercompare results from the two methods to gain a comprehensive understanding of the role of emission sources in PM2.5 formation. The results will be compared in terms of the magnitudes and rankings of SS or SA of emitted species and emission groups/areas. GEOS-Chem with AIT is applied over East Asia at a horizontal grid

Semivolatile Particulate Organic Material Southern Africa during SAFARI 2000

Science.gov (United States)

Eatough, D. J.; Eatough, N. L.; Pang, Y.; Sizemore, S.; Kirchstetter, T. W.; Novakov, T.

2005-01-01

During August and September 2000, the University of Washington's Cloud and Aerosol Research Group (CARG) with its Convair-580 research aircraft participated in the Southern African Fire-Atmosphere Research Initiative (SAFARI) 2000 field study in southern Africa. Aboard this aircraft was a Particle Concentrator-Brigham Young University Organic Sampling System (PC-BOSS), which was used to determine semivolatile particulate material with a diffusion denuder sampler. Denuded quartz filters and sorbent beds in series were used to measure nonvolatile and semivolatile materials, respectively. Results obtained with the PC-BOSS are compared to those obtained with conventional quartz-quartz and Teflon-quartz filter pack samplers. Various 10-120 min integrated samples were collected during flights through the h e troposphere, in the atmospheric boundary layer, and in plumes from savanna fires. Significant fine particulate semivolatile organic compounds (SVOC) were found in all samples. The SVOC was not collected by conventional filter pack samplers and therefore would not have been determined in previous studies that used only filter pack samplers. The SVOC averaged 24% of the fine particulate mass in emissions from the fires and 36% of the fine particulate mass in boundary layer samples heavily impacted by aged emissions from savanna fires. Concentrations of fine particulate material in the atmospheric mixed layer heavily impacted by aged savanna frre emissions averaged 130 micrograms per cubic meter. This aerosol was 85% carbonaceous mated.

Household Air Pollution: Sources and Exposure Levels to Fine Particulate Matter in Nairobi Slums

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Kanyiva Muindi

2016-07-01

Full Text Available With 2.8 billion biomass users globally, household air pollution remains a public health threat in many low- and middle-income countries. However, little evidence on pollution levels and health effects exists in low-income settings, especially slums. This study assesses the levels and sources of household air pollution in the urban slums of Nairobi. This cross-sectional study was embedded in a prospective cohort of pregnant women living in two slum areas—Korogocho and Viwandani—in Nairobi. Data on fuel and stove types and ventilation use come from 1058 households, while air quality data based on the particulate matters (PM2.5 level were collected in a sub-sample of 72 households using the DustTrak™ II Model 8532 monitor. We measured PM2.5 levels mainly during daytime and using sources of indoor air pollutions. The majority of the households used kerosene (69.7% as a cooking fuel. In households where air quality was monitored, the mean PM2.5 levels were high and varied widely, especially during the evenings (124.6 µg/m3 SD: 372.7 in Korogocho and 82.2 µg/m3 SD: 249.9 in Viwandani, and in households using charcoal (126.5 µg/m3 SD: 434.7 in Korogocho and 75.7 µg/m3 SD: 323.0 in Viwandani. Overall, the mean PM2.5 levels measured within homes at both sites (Korogocho = 108.9 µg/m3 SD: 371.2; Viwandani = 59.3 µg/m3 SD: 234.1 were high. Residents of the two slums are exposed to high levels of PM2.5 in their homes. We recommend interventions, especially those focusing on clean cookstoves and lighting fuels to mitigate indoor levels of fine particles.

Characterisation of air particulate matter in Klang Valley by neutron activation analysis technique

International Nuclear Information System (INIS)

Mohd Suhaimi Hamzah; Shamsiah Abd Rahman; Mohd Khalid Matori; Abd Khalik Wood

2000-01-01

Air particulate matter is known to affect human health, impairs visibility and can cause climate change. Study on air particulate matter in term of particle size and chemical contents is very important to indicate the quality of air in a sampling area. Information on concentration of important constituents in air particles can be used to identify some of emission sources which contribute to the pollution problem. The data collected may also be, used as a basis to design a strategy in order to overcome the air pollution problem in the area. The study involved sampling of air dust at two stations, one in Bangi and the other in Kuala Lumpur using Gent Stack Sampler units. Each sampler capable of collecting air particle sizes smaller than 2.5 micron (PM 2.5) and between 2.5 - O micron on two different filters simultaneously. The filters were measured for their mass, elemental carbon and elemental concentrations using analytical equipment or techniques including reflectometer and Neutron Activation Analysis. The results of analysis on samples collected in 1997-1998 are discussed. (author)

Organic speciation of size-segregated atmospheric particulate matter

Science.gov (United States)

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

The geocentric particulate distribution: Cometary, asteroidal, or space debris?

Science.gov (United States)

Mcdonnell, J. A. M.; Ratcliff, P. R.

1992-01-01

Definition of the Low Earth Orbit (LEO) particulate environment has been refined considerably with the analysis of data from NASA's Long Duration Exposure Facility (LDEF). Measurements of the impact rates from particulates ranging from sub-micron to millimetres in dimension and, especially, information on their directionality has permitted new scrunity of the sources of the particulates. Modelling of the dynamics of both bound (Earth orbital) and unbound (hyperbolic interplanetary) particulates intercepting LDEF's faces leads to the conclusion that the source is dominantly interplanetary for particle dimensions of greater than some 5 microns diameter; however the anisotropy below this dimension demands lower velocities and is compatible with an orbital component. Characteristics of the LDEF interplanetary component are compatible with familiar meteoroid sources and deep space measurements. Understanding of the orbital component which exceeds the interplanetary flux by a factor of 4 is less clear; although the very small particulates in orbit have been associated with space debris (Lawrance and Brownlee, 1986) this data conflicts with other measurements (McDonnell, Carey and Dixon, 1984) at the same epoch. By analysis of trajectories approaching the Earth and its atmosphere, we have shown that a significant contribution could be captured by aerocapture, i.e., atmospheric drag, from either asteroidal or cometary sources; such enhancement is unlikely however to provide the temporal and spatial fluctuations observed by the LDEF Interplanetary Dust Experiment (Mullholland et al. 1992). A further new mechanism is also examined, that of aerofragmentation capture, where an atmospheric grazing trajectory, which would not normally lead to capture, leads to fragmentation by thermal or mechanical shock; the microparticulates thus created can be injected in large numbers, but only into short-lifetime orbits. The concentration in one particular orbit plane, could explain the

Analysis of trace elements in airborne particulate matters collected in Ankara, Turkey by TXRF

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Durukan I.

2013-04-01

Full Text Available The main focus point of the presented study was the assessment of atmospheric burden of particulate matter and toxic trace metals in the atmosphere of Ankara, Turkey. For this purpose, outdoor samplings were accomplished in the capital city, Ankara. The types of filters, sample collection and sample preparation methods were investigated and optimized. Analyses were provided by the total reflection X-ray fluorescence (TXRF spectroscopic technique in Germany. Spatial and temporal variations of air particulate matter (APM levels in the city were examined. In some stations, APM sampled in according to their size distribution such as PM10 and PM2.5. Elemental characterization of size distributed PM were achieved and evaluated. It was detected that the elements mainly originated from soil in Beytepe station, from soil and solid fuel usage in Kayas station and from traffic and a variety of human activities in Sıhhiye station in air samplings. While the elements of natural origin observed in PM10 fraction, the elements from traffic and human activities were in PM2.5. Eventually, enrichment calculations were performed in order to identify the pollution sources.

Environmental pollution: quantitative analysis of particulate matter (PM10) by SR-TXRF

International Nuclear Information System (INIS)

Moreira, Silvana; Melo Junior, Ariston da Silva; Zucchi, Orgheda Luiza Araujo Domingues; Vives, Ana Elisa Sirito de

2007-01-01

The atmospheric pollution is a concern in the great urban centers, due its association with man pathologies. The Campinas region is one of the most urbanized of the Sao Paulo State and an important industrial center. Thus, due to its location and importance were installed three samplers for particulate material (PM 10 ). One sampler was located in downtown of Campinas city, in an avenue with high vehicular flow. Another sampler was installed in the UNICAMP campus and the third one in Paulinia city, near to REPLAN. For downtown of Campinas city PM 10 concentrations higher than regular air quality established by CETESB (150 μg.m -3 ) was observed. The PM 10 values for Paulinia and downtown of Campinas were higher than Barao Geraldo location. Employing SR-TXRF was possible identify and quantify 19 elements in the particulate material samples. All the measurements were performed at Synchrotron Light Source Laboratory, Campinas, SP. After statistics analysis by principal components and cluster analysis was possible to assemble the elements according emission sources. The dusty soil for coarse fraction contributed with 62%, 51% and 46% for Barao Geraldo, Paulinia and downtown of Campinas, respectively. The vehicular emission was responsible for 16% at downtown Campinas city as expected due to high vehicular flow at sampling place. The vehicular and industrial emissions contributed with 20% and 25%, respectively at Paulinia sampling site. The industrial emissions observed for Barao Geraldo and downtown of Campinas city were 27% and 33%, respectively. (author)

Particulate Matter (Environmental Health Student Portal)

Science.gov (United States)

... that includes curriculum standards, assessments, and lesson rubrics. Sources of Particulate Matter (U.S. Environmental Protection Agency) - Information and activity on interpreting ... U.S. National Library of Medicine National Institutes of Health U.S. Department ...

Characterization of Fine Particulate Matter in Sharjah, United Arab Emirates Using Complementary Experimental Techniques

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Nasser M. Hamdan

2018-04-01

Full Text Available Airborne particulate matter (PM pollutants were sampled from an urban background site in Sharjah, United Arab Emirates. The fine fraction (PM2.5 (particulates with aerodynamic diameters of less than 2.5 μm was collected on 47-mm Teflon filters and analyzed using a combined set of non-destructive techniques in order to provide better understanding of the sources of pollutants and their interaction during transport in the atmosphere. These techniques included gravimetric analysis, equivalent black carbon (EBC, X-ray fluorescence, scanning electron microscopy, and X-ray diffraction. Generally, the PM2.5 concentrations are within the limits set by the World Health Organization (WHO and the United States (US Environmental Protection Agency. The EBC content is in the range of 10–12% of the total PM concentration (2–4 µg m−3, while S (as ammonium sulfate, Ca (as calcite, gypsum, and calcium carbonate, Si (as quartz, Fe, and Al were the major sources of PM pollution. EBC, ammonium sulfate, Zn, V, and Mn originate from anthropogenic sources such as fossil fuel burning, traffic, and industrial emissions. Natural elements such as Ca, Fe, Al, Si, and Ti are due to natural sources such as crustal materials (enhanced during dust episodes and sea salts. The average contribution of natural sources in the total PM2.5 mass concentration over the sampling period is about 40%, and the contribution of the secondary inorganic compounds is about 27% (mainly ammonium sulfate in our case. The remaining 22% is assumed to be secondary organic compounds.

Revisiting source identification, weathering models, and phase discrimination for Exxon Valdez oil

International Nuclear Information System (INIS)

Driskell, W.B.; Payne, J.R.; Shigenaka, G.

2005-01-01

A large chemistry data set for polycyclic aromatic hydrocarbon (PAH) and saturated hydrocarbon (SHC) contamination in sediment, water and tissue samples has emerged in the aftermath of the 1989 Exxon Valdez oil spill in Prince William Sound, Alaska. When the oil was fresh, source identification was a primary objective and fairly reliable. However, source identification became problematic as the oil weathered and its signatures changed. In response to concerns regarding when the impacted area will be clean again, this study focused on developing appropriate tools to confirm hydrocarbon source identifications and assess weathering in various matrices. Previous efforts that focused only on the whole or particulate-phase oil are not adequate to track dissolved-phase signal with low total PAH values. For that reason, a particulate signature index (PSI) and dissolved signature index (DSI) screening tool was developed in this study to discriminate between these 2 phases. The screening tool was used to measure the dissolved or water-soluble fraction of crude oil which occurs at much lower levels than the particulate phase, but which is more widely circulated and equally as important as the particulate oil phase. The discrimination methods can also identify normally-discarded, low total PAH samples which can increase the amount of usable data needed to model other effects of oil spills. 37 refs., 3 tabs., 10 figs

Heavy coal combustion as the dominant source of particulate pollution in Taiyuan, China, corroborated by high concentrations of arsenic and selenium in PM10

International Nuclear Information System (INIS)

Xie, RuiKai; Seip, Hans Martin; Wibetoe, Grethe; Nori, Showan; McLeod, Cameron William

2006-01-01

Coal burning generates toxic elements, some of which are characteristic of coal combustion such as arsenic and selenium, besides conventional coal combustion products. Airborne particulate samples with aerodynamic diameter less than 10 μm (PM 10 ) were collected in Taiyuan, China, and multi-element analyses were performed by inductively coupled plasma atomic emission spectrometry (ICP-AES) and inductively coupled plasma mass spectrometry (ICP-MS). Concentrations of arsenic and selenium from ambient air in Taiyuan (average 43 and 58 ng m -3 , respectively) were relatively high compared to what is reported elsewhere. Arsenic and selenium were found to be highly correlated (r=0.997), indicating an overwhelmingly dominant source. Correlation between these two chalcophile elements and the lithophile element Al is high (r is 0.75 and 0.72 for As and Se, respectively). This prompted the hypothesis that the particles were from coal combustion. The enrichment of the trace elements could be explained by the volatilization-condensation mechanism during coal combustion process. Even higher correlations of arsenic and selenium with PM 10 (r=0.90 and 0.88) give further support that airborne particulate pollution in Taiyuan is mainly a direct result of heavy coal consumption. This conclusion agrees with the results from our previous study of individual airborne particles in Taiyuan. (author)

The new Chalk River AMS ion source, sample changer and external sample magazine

International Nuclear Information System (INIS)

Koslowsky, V.T.; Bray, N.; Imahori, Y.; Andrews, H.R.; Davies, W.G.

1997-01-01

A new sample magazine, sample changer and ion source have been developed and are in routine use at Chalk River. The system features a readily accessible 40-sample magazine at ground potential that is external to the ion source and high-voltage cage. The samples are held in an inert atmosphere and can be individually examined or removed; they can be exchanged en masse as a complete magazine concurrent with an AMS measurement. On-line sample changing is done with a pneumatic rabbit transfer system employing two stages of differential pumping. At Chalk River this is routinely performed across a 200 kV potential. Sample positioning is precise, and hundreds of 36 Cl and 129 I samples have been measured over a period of several days without interruption or alteration of ion source operating conditions. (author)

PM10 standards and nontraditional particulate source controls: A summary of the A ampersand WMA/EPA international specialty conference

International Nuclear Information System (INIS)

Chow, J.C.; Watson, J.G.; Ono, D.M.; Mathai, C.V.

1993-01-01

An international specialty conference, jointly sponsored by the Air ampersand Waste Management Association (A ampersand WMA) and the US Environmental Protection Agency (EPA), entitled open-quotes PM 10 Standards and Nontraditional Particulate Source Controls,close quotes was held in Scottsdale, Arizona, January 12-15, 1992. The conference included 92 presentations in 17 technical sessions. Eight-one peer-reviewed technical papers, two keynote addresses and one panel session summary describing novel applications, measurement processes, modeling techniques and control measures for nontraditional pollution sources are assembled in the Transactions. The technical issues addressed during the conference included: (1) measurement methods and data bases; (2) emissions source characterization; (3) source apportionment of nontraditional sources; (4) fugitive dust characterization and control technologies; (5) vegetative burning characterization and control technologies; (6) sources and controls of secondary aerosol and motor vehicle precursors; and (7) regulatory policies and State Implementation Plan (SIP) development. This paper gives an overview of the technical program. 105 refs., 1 tab

Design and laboratory testing of a new flow-through directional passive air sampler for ambient particulate matter.

Science.gov (United States)

Lin, Chun; Solera Garcia, Maria Angeles; Timmis, Roger; Jones, Kevin C

2011-03-01

A new type of directional passive air sampler (DPAS) is described for collecting particulate matter (PM) in ambient air. The prototype sampler has a non-rotating circular sampling tray that is divided into covered angular channels, whose ends are open to winds from sectors covering the surrounding 360°. Wind-blown PM from different directions enters relevant wind-facing channels, and is retained there in collecting pools containing various sampling media. Information on source direction and type can be obtained by examining the distribution of PM between channels. Wind tunnel tests show that external wind velocities are at least halved over an extended area of the collecting pools, encouraging PM to settle from the air stream. Internal and external wind velocities are well-correlated over an external velocity range of 2.0-10.0 m s⁻¹, which suggests it may be possible to relate collected amounts of PM simply to ambient concentrations and wind velocities. Measurements of internal wind velocities in different channels show that velocities decrease from the upwind channel round to the downwind channel, so that the sampler effectively resolves wind directions. Computational fluid dynamics (CFD) analyses were performed on a computer-generated model of the sampler for a range of external wind velocities; the results of these analyses were consistent with those from the wind tunnel. Further wind tunnel tests were undertaken using different artificial particulates in order to assess the collection performance of the sampler in practice. These tests confirmed that the sampler can resolve the directions of sources, by collecting particulates preferentially in source-facing channels.

Factors influencing mobile source particulate matter emissions-to-exposure relationships in the Boston urban area.

Science.gov (United States)

Greco, Susan L; Wilson, Andrew M; Hanna, Steven R; Levy, Jonathan I

2007-11-15

Benefit-cost and regulatory impact analyses often use atmospheric dispersion models with coarse resolution to estimate the benefits of proposed mobile source emission control regulations. This approach may bias health estimates or miss important intra-urban variability for primary air pollutants. In this study, we estimate primary fine particulate matter (PM2.5) intake fractions (iF; the fraction of a pollutant emitted from a source that is inhaled by the population) for each of 23 398 road segments in the Boston Metro Core area to evaluate the potential for intra-urban variability in the emissions-to-exposure relationship. We estimate iFs using the CAL3QHCR line source model combined with residential populations within 5000 m of each road segment. The annual average values for the road segments range from 0.8 to 53 per million, with a mean of 12 per million. On average, 46% of the total exposure is realized within 200 m of the road segment, though this varies from 0 to 93% largely due to variable population patterns. Our findings indicate the likelihood of substantial intra-urban variability in mobile source primary PM2.5 iF that accounting for population movement with time, localized meteorological conditions, and street-canyon configurations would likely increase.

A Comparison of the Health Effects of Ambient Particulate Matter Air Pollution from Five Emission Sources

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Neil J. Hime

2018-06-01

Full Text Available This article briefly reviews evidence of health effects associated with exposure to particulate matter (PM air pollution from five common outdoor emission sources: traffic, coal-fired power stations, diesel exhaust, domestic wood combustion heaters, and crustal dust. The principal purpose of this review is to compare the evidence of health effects associated with these different sources with a view to answering the question: Is exposure to PM from some emission sources associated with worse health outcomes than exposure to PM from other sources? Answering this question will help inform development of air pollution regulations and environmental policy that maximises health benefits. Understanding the health effects of exposure to components of PM and source-specific PM are active fields of investigation. However, the different methods that have been used in epidemiological studies, along with the differences in populations, emission sources, and ambient air pollution mixtures between studies, make the comparison of results between studies problematic. While there is some evidence that PM from traffic and coal-fired power station emissions may elicit greater health effects compared to PM from other sources, overall the evidence to date does not indicate a clear ‘hierarchy’ of harmfulness for PM from different emission sources. Further investigations of the health effects of source-specific PM with more advanced approaches to exposure modeling, measurement, and statistics, are required before changing the current public health protection approach of minimising exposure to total PM mass.

Report Task 2.3: Particulate waste and turbidity in (marine) RAS

OpenAIRE

Kals, J.; Schram, E.; Brummelhuis, E.B.M.; Bakel, van, B.

2006-01-01

Particulate waste management and removal is one of the most problematic parts of recirculation aquaculture systems (RAS). Particulate waste and thereby turbidity originates from three major sources: fish (faeces), feed and biofilm (heterotrophic bacteria and fungi). Based on size and density there are roughly four categories of particulate waste: settable, suspended, floatable and fine or dissolved solids. Specific problems related to high turbidity are a decreasing feed intake by fish, causi...

Report Task 2.3: Particulate waste and turbidity in (marine) RAS

NARCIS (Netherlands)

Kals, J.; Schram, E.; Brummelhuis, E.B.M.; Bakel, van B.

2006-01-01

Particulate waste management and removal is one of the most problematic parts of recirculation aquaculture systems (RAS). Particulate waste and thereby turbidity originates from three major sources: fish (faeces), feed and biofilm (heterotrophic bacteria and fungi). Based on size and density there

Novel mass spectrometric instrument for gaseous and particulate characterization and monitoring

International Nuclear Information System (INIS)

Coggiola, M.J.

1993-04-01

Under contract DE-AC21-92MC29116, SRI International will develop a unique new instrument that will be capable of providing real-time (< l minute), quantitative, chemical characterization of gaseous and particulate pollutants generated from DOE waste cleanup activities. The instrument will be capable of detecting and identifying volatile organic compounds, polynuclear aromatic hydrocarbons, heavy metals, and transuranic species released during waste cleanup activities. The instrument will be unique in its ability to detect and quantify in real-time these diverse pollutants in both vapor and particulate form. The instrument to be developed under this program will consist of several major components: (1) an isokinetic sampler capable of operating over a wide range of temperatures (up to 500 K) and flow rates; (2) a high pressure to low pressure transition and sampling region that efficiently separates particles from vapor-phase components for separate, parallel analyses; (3) two small mass spectrometers, one optimized for organic analysis using a unique field ionization source and one optimized for particulate characterization using thermal pyrolysis and electron-impact ionization (EI); and (4) a powerful personal computer for control and data acquisition

Chemical characterization and sources of personal exposure to fine particulate matter in the general population of Guangzhou, China

Science.gov (United States)

Chen, Xiao-Cui; Jahn, Heiko J.; Engling, Guenter; Ward, Tony J.; Kraemer, Alexander; Ho, Kin-Fai; Hung-Lam Yim, Steve; Chan, Chuen-Yu

2017-04-01

Fine particulate matter pollution severely deteriorates the environmental conditions and negatively impacts human health in the Chinese megacity Guangzhou. Concurrent ambient and personal measurements of fine particulate matter (PM2.5) were conducted in Guangzhou, China. Personal-to-ambient (P-C) relationships of PM2.5 chemical components were determined and sources of personal PM2.5 exposure were evaluated using principal component analysis along with a mixed-effects model. Water-soluble inorganic ions (mainly secondary inorganic ions) and anhydrosugars exhibited median personal-to-ambient (P/C) ratios < 1 accompanied by strong P-C correlations, indicating that these constituents in personal PM2.5 were significantly affected by ambient sources. Conversely, elemental carbon (EC) and calcium (Ca2+) showed median P/C ratios greater than unity, which indicated that among subjects who spent a great amount of time indoors, aside from particles of ambient origin, individual's total exposure to PM2.5 includes contributions of non-ambient exposure while indoors and outdoors (e.g., local traffic, indoor sources, personal activities). SO42- displayed very low coefficient of divergence (COD) values coupled with strong P-C correlations, implying a uniform distribution of SO42- in the urban area of Guangzhou. EC, Ca2+, and levoglucosan were otherwise heterogeneously distributed across individuals in different districts. Regional air pollution (50.4 ± 0.9%), traffic-related particles (8.6 ± 0.7%), dust-related particles (5.8 ± 0.7%), and biomass burning emissions (2.0 ± 0.2%) were moderate to high positive sources of personal PM2.5 exposure in Guangzhou. The observed positive and significant contribution of Ca2+ to personal PM2.5 exposure, highlighting indoor sources and/or personal activities, were driving factors determining personal exposure to dust-related particles. Considerable discrepancies (COD values ranging from 0.42 to 0.50) were shown between ambient

Chemical characterization and stable carbon isotopic composition of particulate Polycyclic Aromatic Hydrocarbons issued from combustion of 10 Mediterranean woods

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A. Guillon

2013-03-01

Full Text Available The objectives of this study were to characterize polycyclic aromatic hydrocarbons from particulate matter emitted during wood combustion and to determine, for the first time, the isotopic signature of PAHs from nine wood species and Moroccan coal from the Mediterranean Basin. In order to differentiate sources of particulate-PAHs, molecular and isotopic measurements of PAHs were performed on the set of wood samples for a large panel of compounds. Molecular profiles and diagnostic ratios were measured by gas chromatography/mass spectrometry (GC/MS and molecular isotopic compositions (δ13C of particulate-PAHs were determined by gas chromatography/combustion/isotope ratio mass spectrometry (GC/C/IRMS. Wood species present similar molecular profiles with benz(aanthracene and chrysene as dominant PAHs, whereas levels of concentrations range from 1.8 to 11.4 mg g−1 OC (sum of PAHs. Diagnostic ratios are consistent with reference ratios from literature but are not sufficient to differentiate the species of woods. Concerning isotopic methodology, PAH molecular isotopic compositions are specific for each species and contrary to molecular fingerprints, significant variations of δ13C are observed for the panel of PAHs. This work allows differentiating wood combustion (with δ13CPAH = −28.7 to −26.6‰ from others origins of particulate matter (like vehicular exhaust using isotopic measurements but also confirms the necessity to investigate source characterisation at the emission in order to help and complete source assessment models. These first results on woodburnings will be useful for the isotopic approach to source tracking.

Chemical characterization of freshly emitted particulate matter from aircraft exhaust using single particle mass spectrometry

Science.gov (United States)

Abegglen, Manuel; Brem, B. T.; Ellenrieder, M.; Durdina, L.; Rindlisbacher, T.; Wang, J.; Lohmann, U.; Sierau, B.

2016-06-01

Non-volatile aircraft engine emissions are an important anthropogenic source of soot particles in the upper troposphere and in the vicinity of airports. They influence climate and contribute to global warming. In addition, they impact air quality and thus human health and the environment. The chemical composition of non-volatile particulate matter emission from aircraft engines was investigated using single particle time-of-flight mass spectrometry. The exhaust from three different aircraft engines was sampled and analyzed. The soot particulate matter was sampled directly behind the turbine in a test cell at Zurich Airport. Single particle analyses will focus on metallic compounds. The particles analyzed herein represent a subset of the emissions composed of the largest particles with a mobility diameter >100 nm due to instrumental restrictions. A vast majority of the analyzed particles was shown to contain elemental carbon, and depending on the engine and the applied thrust the elemental carbon to total carbon ratio ranged from 83% to 99%. The detected metallic compounds were all internally mixed with the soot particles. The most abundant metals in the exhaust were Cr, Fe, Mo, Na, Ca and Al; V, Ba, Co, Cu, Ni, Pb, Mg, Mn, Si, Ti and Zr were also detected. We further investigated potential sources of the ATOFMS-detected metallic compounds using Inductively Coupled Plasma Mass Spectrometry. The potential sources considered were kerosene, engine lubrication oil and abrasion from engine wearing components. An unambiguous source apportionment was not possible because most metallic compounds were detected in several of the analyzed sources.

Particulate emission factor: A case study of a palm oil mill boiler

International Nuclear Information System (INIS)

Chong, W.C.; Rashid, M.; Ramli, M.; Zainura, Z.N.; NorRuwaida, J.

2010-01-01

A study to investigate the particulate emission from a boiler of a palm oil mill plant equipped with a multi-cyclones particulate arrest or was performed and reported in this paper. The particulate emission concentration was measured at the outlet of a 8 mt/ hr capacity water-tube typed boiler of a palm oil mill plant processing 27mt/ hr of fresh fruit bunch (FFB). The particulate sample was collected iso-kinetically using the USEPA method 5 sampling train through a sampling port made at the duct of the exiting flue gas between the boiler and a multi-cyclones unit. Results showed that the particulate emission rates exiting the boiler varied from 0.09 to 0.60 g/s with an average of 0.29 + 0.18 g/ s. While the average particulate emission concentration exiting the boiler was 12.1 + 7.36 g/ Nm 3 (corrected to 7 % oxygen concentration), ranging from 3.62 to 25.3 g/ Nm 3 (at 7 % O 2 ) of the flue gas during the measurement. Based on the 27 mt/ hr FFB processed and the capacity of the boiler of 8mt steam/ hr, the calculated particulate emission factor was 39 g particulate/ mt FFB processed or 131 g particulate/ mt boiler capacity, respectively. In addition, based on the finding and in order to comply with the emission limits of 0.4 g/ Nm 3 , the collection efficiency of any given particulate emission pollution control system to consider for the mill will be from 87 to 98 %, which is not easily achievable with the existing multi-cyclones unit. A considerable amount of efforts are still needed pertaining to the particulate emission control problem in the industry. (author)

Cause-specific stillbirth and exposure to chemical constituents and sources of fine particulate matter.

Science.gov (United States)

Ebisu, Keita; Malig, Brian; Hasheminassab, Sina; Sioutas, Constantinos; Basu, Rupa

2018-01-01

The stillbirth rate in the United States is relatively high, but limited evidence is available linking stillbirth with fine particulate matter (PM 2.5 ), its chemical constituents and sources. In this study, we explored associations between cause-specific stillbirth and prenatal exposures to those pollutants with using live birth and stillbirth records from eight California locations during 2002-2009. ICD-10 codes were used to identify cause of stillbirth from stillbirth records. PM 2.5 total mass and chemical constituents were collected from ambient monitors and PM 2.5 sources were quantified using Positive Matrix Factorization. Conditional logistic regression was applied using a nested case-control study design (N = 32,262). We found that different causes of stillbirth were associated with different PM 2.5 sources and/or chemical constituents. For stillbirths due to fetal growth, the odds ratio (OR) per interquartile range increase in gestational age-adjusted exposure to PM 2.5 total mass was 1.23 (95% confidence interval (CI): 1.06, 1.44). Similar associations were found with resuspended soil (OR=1.25, 95% CI: 1.10, 1.42), and secondary ammonium sulfate (OR=1.45, 95% CI: 1.18, 1.78). No associations were found between any pollutants and stillbirths caused by maternal complications. This study highlighted the importance of investigating cause-specific stillbirth and the differential toxicity levels of specific PM 2.5 sources and chemical constituents. Copyright © 2017 Elsevier Inc. All rights reserved.

Evolution of the Lunar Receiving Laboratory to the Astromaterial Sample Curation Facility: Technical Tensions Between Containment and Cleanliness, Between Particulate and Organic Cleanliness

Science.gov (United States)

Allton, J. H.; Zeigler, R. A.; Calaway, M. J.

2016-01-01

The Lunar Receiving Laboratory (LRL) was planned and constructed in the 1960s to support the Apollo program in the context of landing on the Moon and safely returning humans. The enduring science return from that effort is a result of careful curation of planetary materials. Technical decisions for the first facility included sample handling environment (vacuum vs inert gas), and instruments for making basic sample assessment, but the most difficult decision, and most visible, was stringent biosafety vs ultra-clean sample handling. Biosafety required handling of samples in negative pressure gloveboxes and rooms for containment and use of sterilizing protocols and animal/plant models for hazard assessment. Ultra-clean sample handling worked best in positive pressure nitrogen environment gloveboxes in positive pressure rooms, using cleanable tools of tightly controlled composition. The requirements for these two objectives were so different, that the solution was to design and build a new facility for specific purpose of preserving the scientific integrity of the samples. The resulting Lunar Curatorial Facility was designed and constructed, from 1972-1979, with advice and oversight by a very active committee comprised of lunar sample scientists. The high precision analyses required for planetary science are enabled by stringent contamination control of trace elements in the materials and protocols of construction (e.g., trace element screening for paint and flooring materials) and the equipment used in sample handling and storage. As other astromaterials, especially small particles and atoms, were added to the collections curated, the technical tension between particulate cleanliness and organic cleanliness was addressed in more detail. Techniques for minimizing particulate contamination in sample handling environments use high efficiency air filtering techniques typically requiring organic sealants which offgas. Protocols for reducing adventitious carbon on sample

Environmental studies in two communes of Santiago de Chile by the analysis of magnetic properties of particulate matter deposited on leaves of roadside trees

Science.gov (United States)

Muñoz, David; Aguilar, Bertha; Fuentealba, Raúl; Préndez, Margarita

2017-03-01

Emissions from motor vehicles are considered to be one of the main sources of airborne particulate matter in Santiago. International researchers have shown that particulate matter contains metal oxides and magnetic particles, both of which are emitted mainly from vehicles exhaust pipes. On the other hand, trees are effective in reducing such contamination, so that they act as passive collectors of particulate matter. This work presents the results obtained from the first magnetic study of the particulate matter collected in two areas of the city of Santiago de Chile. Magnetic susceptibility and Saturation Isothermic Remanent Magnetization (SIRM) were determined in leaves from abundant urban trees and from urban dust samples. Results indicate that most of the samples contain ferromagnetic minerals with magnetite (Fe3O4) as the main carrier. Values of magnetic susceptibility (SI ×10-6 m3/kg) in the range 0.04-0.24 for leaves and in the range 10-45 for urban dust were determinated. In one of the city areas studied, significant correlation between the particulate matter deposited on leaves of Platanus orientalis and measured traffic flows was obtained. In addition, it was possible to estimate that the species Platanus orientalis and Acer negundo have a better ability to capture particulate matter than the species Robinia pseudoacacia.

Directional dependency of air sampling

International Nuclear Information System (INIS)

1994-01-01

A field study was performed by Idaho State University-Environmental Monitoring Laboratory (EML) to examine the directional dependency of low-volume air samplers. A typical continuous low volume air sampler contains a sample head that is mounted on the sampler housing either horizontally through one of four walls or vertically on an exterior wall 'looking down or up.' In 1992, a field study was undertaken to estimate sampling error and to detect the directional effect of sampler head orientation. Approximately 1/2 mile downwind from a phosphate plant (continuous source of alpha activity), four samplers were positioned in identical orientation alongside one sampler configured with the sample head 'looking down'. At least five consecutive weekly samples were collected. The alpha activity, beta activity, and the Be-7 activity collected on the particulate filter were analyzed to determine sampling error. Four sample heads were than oriented to the four different horizontal directions. Samples were collected for at least five weeks. Analysis of the alpha data can show the effect of sampler orientation to a know near source term. Analysis of the beta and Be-7 activity shows the effect of sampler orientation to a ubiquitous source term

Long-term particulate matter modeling for health effect studies in California - Part 2: Concentrations and sources of ultrafine organic aerosols

Science.gov (United States)

Hu, Jianlin; Jathar, Shantanu; Zhang, Hongliang; Ying, Qi; Chen, Shu-Hua; Cappa, Christopher D.; Kleeman, Michael J.

2017-04-01

Organic aerosol (OA) is a major constituent of ultrafine particulate matter (PM0. 1). Recent epidemiological studies have identified associations between PM0. 1 OA and premature mortality and low birth weight. In this study, the source-oriented UCD/CIT model was used to simulate the concentrations and sources of primary organic aerosols (POA) and secondary organic aerosols (SOA) in PM0. 1 in California for a 9-year (2000-2008) modeling period with 4 km horizontal resolution to provide more insights about PM0. 1 OA for health effect studies. As a related quality control, predicted monthly average concentrations of fine particulate matter (PM2. 5) total organic carbon at six major urban sites had mean fractional bias of -0.31 to 0.19 and mean fractional errors of 0.4 to 0.59. The predicted ratio of PM2. 5 SOA / OA was lower than estimates derived from chemical mass balance (CMB) calculations by a factor of 2-3, which suggests the potential effects of processes such as POA volatility, additional SOA formation mechanism, and missing sources. OA in PM0. 1, the focus size fraction of this study, is dominated by POA. Wood smoke is found to be the single biggest source of PM0. 1 OA in winter in California, while meat cooking, mobile emissions (gasoline and diesel engines), and other anthropogenic sources (mainly solvent usage and waste disposal) are the most important sources in summer. Biogenic emissions are predicted to be the largest PM0. 1 SOA source, followed by mobile sources and other anthropogenic sources, but these rankings are sensitive to the SOA model used in the calculation. Air pollution control programs aiming to reduce the PM0. 1 OA concentrations should consider controlling solvent usage, waste disposal, and mobile emissions in California, but these findings should be revisited after the latest science is incorporated into the SOA exposure calculations. The spatial distributions of SOA associated with different sources are not sensitive to the choice of

Principal component analysis of air particulate data from the industrial area of islamabad, pakistan

International Nuclear Information System (INIS)

Waheed, S.; Siddique, N.; Daud, M.

2008-01-01

A Gent air sampler was used to collect 72 pairs of size fractionated coarse and fine (PM/sub 10/ and PM/sub 2.5/) particulate mass samples from the industrial zone (sector I-9) of Islamabad. These samples were analyzed for their elemental composition using Instrumental Neutron Activation Analysis (INAA). Principal component analysis (PCA), which can be used for source apportionment of quantified elemental data, was used to interpret the data. Graphical representations of loadings were used to explain the data through grouping of the elements from same source. The present work shows well defined elemental fingerprints of suspended soil and road dust, industry, motor vehicle exhaust and tyres, and coal and refuses combustions for the studied locality of Islamabad. (author)

Relation between sources of particulate air pollution and biological effect parameters in samples from four European cities: An exploratory study

Energy Technology Data Exchange (ETDEWEB)

Steerenberg, P.A.; van Amelsvoort, L.; Lovik, M.; Hetland, R.B.; Alberg, T.; Halatek, T.; Bloemen, H.J.T.; Rydzynski, K.; Swaen, G.; Schwarze, P.; Dybing, E.; Cassee, F.R. [National Institute of Public Health & Environment, Bilthoven (Netherlands). Centre for Environmental Health Research

2006-05-15

Given that there are widely different prevalence rates of respiratory allergies and asthma between the countries of Europe and that exposure to ambient particulate matter (PM) is substantial in urban environments throughout Europe, an EU project entitled 'Respiratory Allergy and Inflammation Due to Ambient Particles' (RAIAP) was set up. The project focused on the role of physical and chemical composition of PM on release of cytokines of cells in vitro, on respiratory inflammation in vivo, and on adjuvant potency in allergy animal models. Coarse (2.5 - 10 {mu}m) and fine (0.15 - 2.5 {mu}m) particles were collected during the spring, summer and winter in Rome ( I), Oslo (N), Lodz (PL), and Amsterdam (NL). Markers within the same model were often well correlated. Markers of inflammation in the in vitro and in vivo models also showed a high degree of correlation. In contrast, correlation between parameters in the different allergy models and between allergy and inflammation markers was generally poor. This suggests that various bioassays are needed to assess the potential hazard of PM. The present study also showed that by clustering chemical constituents of PM based on the overall response pattern in the bioassays, five distinct groups could be identified. The clusters of traffic, industrial combustion and/or incinerators, and combustion of black and brown coal/wood smoke were associated primarily with adjuvant activity for respiratory allergy, whereas clusters of crustal of material and sea spray are predominantly associated with measures for inflammation and acute toxicity. The present study has shown that biological effect of PM can be linked to one or more PM emission sources and that this linkage requires a wide range of bioassays.

The evaluation of a ceramic diesel particulate filter in an underground mine laboratory

International Nuclear Information System (INIS)

Carlson, D.H.; Bucheger, D.; Patton, M.; Johnson, J.H.

1986-01-01

This paper details the collection of diesel exhaust particulate from the instrumented Wagner ST5A load-haul-dump vehicle during a simulated ore loading and hauling operation. An evaluation of the exhaust included measurements to determine the effect of the Corning diesel particulate filter (DPF) on air quality, and the effect of operating variables and fuel additives on DPF regeneration. The results demonstrate the important effects of other mine particulate sources on the particulate collection efficiency

Gamma spectrometric analyses of environmental samples at PINSTECH

International Nuclear Information System (INIS)

Faruq, M.U.; Parveen, N.; Ahmed, B.; Aziz, A.

1979-01-01

Gamma spectrometric analyses of air and other environmental samples from PINSTECH were carried out. Air particulate samples were analyzed by a Ge(Li) detector on a computer-based multichannel analyzer. Other environmental samples were analyzed by a Na(T1) scintillation detector spectrometer and a multichannel analyzer with manual analysis. Concentration of radionuclides in the media was determined and the sources of their production were identified. Age of the fall out was estimated from the ratios of the fission products. (authors)

An Application Of Receptor Modeling To Identify Airborne Particulate ...

African Journals Online (AJOL)

An Application Of Receptor Modeling To Identify Airborne Particulate Sources In Lagos, Nigeria. FS Olise, OK Owoade, HB Olaniyi. Abstract. There have been no clear demarcations between industrial and residential areas of Lagos with focus on industry as the major source. There is need to identify potential source types in ...

An overview of particulate emissions from residential biomass combustion

Science.gov (United States)

Vicente, E. D.; Alves, C. A.

2018-01-01

Residential biomass burning has been pointed out as one of the largest sources of fine particles in the global troposphere with serious impacts on air quality, climate and human health. Quantitative estimations of the contribution of this source to the atmospheric particulate matter levels are hard to obtain, because emission factors vary greatly with wood type, combustion equipment and operating conditions. Updated information should improve not only regional and global biomass burning emission inventories, but also the input for atmospheric models. In this work, an extensive tabulation of particulate matter emission factors obtained worldwide is presented and critically evaluated. Existing quantifications and the suitability of specific organic markers to assign the input of residential biomass combustion to the ambient carbonaceous aerosol are also discussed. Based on these organic markers or other tracers, estimates of the contribution of this sector to observed particulate levels by receptor models for different regions around the world are compiled. Key areas requiring future research are highlighted and briefly discussed.

Evaluation of Pollution of Soils and Particulate Matter Around Metal Recycling Factories in Southwestern Nigeria

OpenAIRE

Akinade S. Olatunji; Tesleem O. Kolawole; Moroof Oloruntola; Christina Günter

2018-01-01

Background. Metal recycling factories (MRFs) have developed rapidly in Nigeria as recycling policies have been increasingly embraced. These MRFs are point sources for introducing potentially toxic elements (PTEs) into environmental media. Objectives. The aim of this study was to determine the constituents (elemental and mineralogy) of the wastes (slag and particulate matter, (PM)) and soils around the MRFs and to determine the level of pollution within the area. Methods. Sixty samples (...

Winter fine particulate air quality in Cranbrook, British Columbia, 1973 to 1999

International Nuclear Information System (INIS)

McDonald, L.E.

2001-06-01

Fine particulate levels in Cranbrook, BC, are analyzed and reported based on monitoring records which began in 1973. Prior to 1988 the sampler collected all particle sizes, but was subsequently replaced with a selective size inlet to capture only PM 1 0 particles or smaller. A mathematical relationship was produced and used to convert historical total suspended particulates measurements to PM 1 0. It was determined that only monitoring records obtained during the winter months could be reliably converted in this fashion; however, that was not a problem since the winter months happen to correspond to the highest levels of fine particulates. Results of the analysis showed increased levels of PM 1 0 from the early 1970s to the early 1980s; during this time average and maximum annual PM 1 0 levels in Cranbrook were higher than those in Los Angeles in 1999. Winter PM 1 0 levels began to fall through the late 1980s and early 1990s. The lowest average and maximum (18 microgram/cubic metre and 47 microgram/cubic metre, respectively) was recorded in the winter of 1996/1997. Worst conditions were recorded in 1980/1981 when 15 of 21 samples exceeded the current provincial PM 1 0 air quality objective of 50 microgram/cubic metre. In the five winters between 1994/1995 and 1998/1999 only three of 109 samples exceeded the provincial objective. There appears to be no correlation between known changes in industrial and mobile sources of pollutants and historical patterns of fine particulate air pollution in Cranbrook, BC. Observation and experience over three decades suggest that the major source of PM 1 0 in Cranbrook was combustion of wood for home heating. The most probable major cause of the improvements in winter air quality was identified as the gradual conversion from wood to natural gas fired appliances through the 1980s and the 1990s. The 115 per cent increase in the cost of natural gas in the last two years unfortunately, will again make wood an attractive alternative

Particulate hot gas stream cleanup technical issues

Energy Technology Data Exchange (ETDEWEB)

Pontius, D.H.; Snyder, T.R.

1999-09-30

The analyses of hot gas stream cleanup particulate samples and descriptions of filter performance studied under this contract were designed to address problems with filter operation that have been linked to characteristics of the collected particulate matter. One objective of this work was to generate an interactive, computerized data bank of the key physical and chemical characteristics of ash and char collected from operating advanced particle filters and to relate these characteristics to the operation and performance of these filters. The interactive data bank summarizes analyses of over 160 ash and char samples from fifteen pressurized fluidized-bed combustion and gasification facilities utilizing high-temperature, high pressure barrier filters.

Determination of Selected Polycyclic Aromatic Compounds in Particulate Matter Samples with Low Mass Loading: An Approach to Test Method Accuracy

Directory of Open Access Journals (Sweden)

Susana García-Alonso

2017-01-01

Full Text Available A miniaturized analytical procedure to determine selected polycyclic aromatic compounds (PACs in low mass loadings (<10 mg of particulate matter (PM is evaluated. The proposed method is based on a simple sonication/agitation method using small amounts of solvent for extraction. The use of a reduced sample size of particulate matter is often limiting for allowing the quantification of analytes. This also leads to the need for changing analytical procedures and evaluating its performance. The trueness and precision of the proposed method were tested using ambient air samples. Analytical results from the proposed method were compared with those of pressurized liquid and microwave extractions. Selected PACs (polycyclic aromatic hydrocarbons (PAHs and nitro polycyclic aromatic hydrocarbons (NPAHs were determined by liquid chromatography with fluorescence detection (HPLC/FD. Taking results from pressurized liquid extractions as reference values, recovery rates of sonication/agitation method were over 80% for the most abundant PAHs. Recovery rates of selected NPAHs were lower. Enhanced rates were obtained when methanol was used as a modifier. Intermediate precision was estimated by data comparison from two mathematical approaches: normalized difference data and pooled relative deviations. Intermediate precision was in the range of 10–20%. The effectiveness of the proposed method was evaluated in PM aerosol samples collected with very low mass loadings (<0.2 mg during characterization studies from turbofan engine exhausts.

Determination of particulate lead during MILAGRO / MCMA-2006 using Aerosol Mass Spectrometry

Science.gov (United States)

Salcedo, Dara; Onasch, T. B.; Aiken, A. C.; Williams, L. R.; de Foy, B.; Cubison, M. J.; Worsnop, D. R.; Molina, L. T.; Jimenez, J. L.

2010-05-01

We report the first measurements of particulate lead (Pb) from Aerodyne Aerosol Mass Spectrometers, which were deployed in and around Mexico City during the Megacity Initiative: Local and Global Research Observations (MILAGRO) / Mexico City Metropolitan Area 2006 (MCMA-2006) field campaigns. The high resolution mass spectrometer of one of the AMS instruments (HR-AMS) and the measured isotopic ratios unequivocally prove the detection of Pb in ambient particles. A substantial fraction of the lead evaporated slowly from the vaporizer of the instruments, which is indicative of species with low volatility at 600oC. A model was developed in order to estimate the ambient particulate Pb entering the AMS from the signals in the "open" and the "closed" (or "background") mass spectrum modes of the AMS. The model suggests the presence of at least two lead fractions with ~25% of the Pb signal exhibiting rapid evaporation (1/e decay constant, τ PEMEX32 site). From laboratory experiments with pure Pb(NO3)2 particles, we estimated that the Pb ionization efficiency relative to nitrate (RIEPb) is 0.5. Comparison of time series of AMS Pb with other measurements carried out at the T0 urban supersite during MILAGRO (using Proton Induced X-ray Emission (PIXE), Inductively-Coupled Plasma Mass Spectrometry (ICP-MS) and single-particle counts from an Aerosol Time-of-Fight Mass Spectrometer (ATOFMS)) shows similar levels (for PIXE and ICP-MS) and substantial correlation. During part of the campaign, sampling at T0 was alternated every 10 minutes with an Aerosol Concentrator, which enabled the detection of signals for PbCl+ and PbS+ ions. PbS+ displays the signature of a slowly evaporating species, while PbCl+ appears to arise only from fast evaporation, which is likely due to the higher vapor pressure of the compounds generating PbCl+. This is consistent with the evaporation model results. Levels of particulate Pb measured during MILAGRO at T0 were similar to previous studies in Mexico

Determination of particulate lead using aerosol mass spectrometry: MILAGRO/MCMA-2006 observations

Science.gov (United States)

Salcedo, D.; Onasch, T. B.; Aiken, A. C.; Williams, L. R.; de Foy, B.; Cubison, M. J.; Worsnop, D. R.; Molina, L. T.; Jimenez, J. L.

2010-06-01

We report the first measurements of particulate lead (Pb) from Aerodyne Aerosol Mass Spectrometers, which were deployed in and around Mexico City during the Megacity Initiative: Local and Global Research Observations (MILAGRO)/Mexico City Metropolitan Area 2006 (MCMA-2006) field campaigns. The high resolution mass spectrometer of one of the AMS instruments (HR-AMS) and the measured isotopic ratios unequivocally prove the detection of Pb in ambient particles. A substantial fraction of the lead evaporated slowly from the vaporizer of the instruments, which is indicative of species with low volatility at 600 °C. A model was developed in order to estimate the ambient particulate Pb entering the AMS from the signals in the "open" and the "closed" (or "background") mass spectrum modes of the AMS. The model suggests the presence of at least two lead fractions with ~25% of the Pb signal exhibiting rapid evaporation (1/e decay constant, τPEMEX site). From laboratory experiments with pure Pb(NO3)2 particles, we estimated that the Pb ionization efficiency relative to nitrate (RIEPb) is 0.5. Comparison of time series of AMS Pb with other measurements carried out at the T0 supersite during MILAGRO (using Proton Induced X-ray Emission (PIXE), Inductively-Coupled Plasma Mass Spectrometry (ICP-MS) and single-particle counts from an Aerosol Time-of-Fight Mass Spectrometer (ATOFMS)) shows similar levels (for PIXE and ICP-MS) and substantial correlation. During part of the campaign, sampling at T0 was alternated every 10 min with an Aerosol Concentrator, which enabled the detection of signals for PbCl+ and PbS+ ions. PbS+ displays the signature of a slowly evaporating species, while PbCl+ appears to arise only from fast evaporation, which is likely due to the higher vapor pressure of the compounds generating PbCl+. This is consistent with the evaporation model results. Levels of particulate Pb measured at T0 were similar to previous studies in Mexico City. Pb shows a diurnal cycle

Determination of trace elements in airborne particulates by instrumental neutron activation analysis

International Nuclear Information System (INIS)

Jung, Yong Sam; Jung, Yung Joo; Jung, Eui Sik; Cho, Seung Yun

1995-01-01

Trace elements in airborne particulates were analyzed by instrumental neutron activation analysis(INAA) under the optimum analytical condition. Neutron irradiation for sample was done at the irradiation hole(neutron flux, 1 x 10 13 n/cm 2 s) of TRIGA MARK-III research reactor in the Korea Atomic Energy Research Institute. For the verification of the analytical method, NIST SRM-1648 and NIES CRM No.8 were chosen and analyzed. The accuracy and precision of the analysis of 40 and 24 trace elements in the samples were compared with the certified and reported values, respectively. The analytical method was found to be reliable enough when the analytical data of NIES sample were compared with those of different countries. In the analytical result of two or both of standard reference materials, relative standard deviation was within the 15% except a few elements and the relative error was within the 10%. We used this method to analyze 30 trace elements in airborne particulates collected with the high volume air sampler(PM-10) at two different locations and also confirmed the possibility to use this method as a routine monitoring tool to find out environmental pollution sources. 3 figs., 8 tabs., 19 refs. (Author)

Air particulate pollution studies in Asian countries using nuclear analytical techniques

International Nuclear Information System (INIS)

Hien, P.D.

1998-01-01

Air particulate pollution is regarded as critical in Asian cities. The levels of suspended particulate matter in major Asian cities far exceed the WHO's guideline. Nuclear analytical techniques have been widely used in the studies of air particulate pollution to provide aerosol elemental compositions for the purpose of deriving the structure of emission sources. This paper presents some preliminary observations and findings based on publications in scientific literatures. Data on PM-10 levels and socio-economic indicators are used for searching a relationship between air quality and the level of development across Asia. An inverse linear relationship between PM-10 levels and logarithm of per capita GDP appears to exist, although there are large fluctuations of data caused by the very different climatic and geographical conditions of cities studied. Soil dust is generally a major, or even predominant aerosol source in Asian cities. Other common sources include vehicular emissions, coal and oil combustion, burning of refuse (in open) and biomass (including forest fires). The relevance and the trends of these sources in Asian context are discussed. Multivariate receptor modelling techniques applied in source characterization are illustrated through the cases of Lahore and Hochiminh City. Although having limitations in dealing with mixing and overlapping sources, receptor modelling based on principal component factor analysis has been proven to be uncomplicated and sufficiently reliable for characterising aerosol sources in urban areas. (author)

Particulate-bound polycyclic aromatic hydrocarbon sources and determinants in residential homes.

Science.gov (United States)

Cattaneo, Andrea; Fermo, Paola; Urso, Patrizia; Perrone, Maria Grazia; Piazzalunga, Andrea; Tarlassi, Jessica; Carrer, Paolo; Cavallo, Domenico Maria

2016-11-01

Human exposure to polycyclic aromatic hydrocarbons (PAHs) in indoor environments can be particularly relevant because people spend most of their time inside buildings, especially in homes. This study aimed to investigate the most important particle-bound PAH sources and exposure determinants in PM 2.5 samples collected in 19 homes located in northern Italy. Complementary information about ion content in PM 10 was also collected in 12 of these homes. Three methods were used for the identification of PAH sources and determinants: diagnostic ratios with principal component and hierarchical cluster analyses (PCA and HCA), chemical mass balance (CMB) and linear mixed models (LMMs). This combined and tiered approach allowed the infiltration of outdoor PAHs into indoor environments to be identified as the most important source in winter, with a relevant role played by biomass burning and traffic exhausts to be identified as a general source of PAHs in both seasons. Tobacco smoke exhibited an important impact on PAH levels in smokers' homes, whereas in the whole sample, cooking food and natural gas sources played a minor or negligible role. Nitrate, sulfate and ammonium were the main inorganic constituents of indoor PM 10 owing to the secondary formation of ammonium sulfates and nitrates. Copyright © 2016 Elsevier Ltd. All rights reserved.

Sampling for diesel particulate matter in mines : Diesel Emissions Evaluation Program (DEEP), technology transfer initiative, October 2001

International Nuclear Information System (INIS)

Grenier, M.; Gangal, M.; Goyer, N.; McGinn, S.; Penney, J.; Vergunst, J.

2001-10-01

The physical and chemical characteristics of diesel particulate matter (DPM) from exhaust gases from diesel powered mining equipment were presented along with guidelines and regulation for exposure monitoring in the workplace. The report addresses issues related to personal and direct exhaust sampling in mines and presents evidence about potential carcinogenicity of the solid fraction of diesel exhaust. The incomplete combustion of diesel fuel results in the formation of solid and liquid particles in the exhaust. DPM is defined as being the portion of diesel exhaust which is made up of solid carbon particles and the attached chemicals such as polycyclic aromatic hydrocarbons and inorganics such as sulphate compounds. DPM is a submicron aerosol and as such, it is a respirable dust which penetrates deep into the lungs. In addition, DPMs are not easily removed from the air stream because of their small size. Control of DPM is crucial because once they are airborne, they are likely to remain that way and will affect the workplace where they are produced as well as workplaces downwind. In January 2001, the Mine Safety and Health Administration issued a ruling for U.S. metal and non-metal mines requiring that mines meet a limit of exposure of 0.40 mg/m 3 . Mines are expected to reduce exposure to meet a 0.16 mg/m 3 limit of exposure by January 2006. European mines and tunnel construction projects must also meet DPM exposure limits. DPM sampling in Canada has been regulated for nearly one decade. Sampling protocols in Canada and the United States were described with reference to equipment and procedures testing DPM filtration efficiency of after-treatment modules and to evaluate the impact of diesel equipment maintenance on gaseous particulate emissions. 23 refs., 1 tab., 7 figs

Estimating particulate matter health impact related to the combustion of different fossil fuels

International Nuclear Information System (INIS)

Kuenen, Jeroen; Kranenburg, Richard; Hendriks, Carlijn; Schaap, Martijn; Gschwind, Benoit; Lefevre, Mireille; Blanc, Isabelle; Drebszok, Kamila; Wyrwa, Artur; Stetter, Daniel

2013-01-01

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. We have successfully generated a web map service that allows to access information on fuel dependent health effects due to particulate matter. For this purpose, the LOTOS-EUROS air pollution model was equipped with a source apportionment module that tracks the origin of the modelled particulate matter distributions thoughout a simulation. Combined with a dedicated emission inventory PM2.5 maps specified by fuel type were generated for 2007-2009. These maps were combined with a health impact calculation to estimate Lost of Life Expectancy for each fuel categories. An user friendly web client was generated to access the results and use the web mapping service in an easy manner. (orig.)

Comparison of particulate matter exposure estimates in young children from personal sampling equipment and a robotic sampler.

Science.gov (United States)

Sagona, Jessica A; Shalat, Stuart L; Wang, Zuocheng; Ramagopal, Maya; Black, Kathleen; Hernandez, Marta; Mainelis, Gediminas

2017-05-01

Accurate characterization of particulate matter (PM) exposure in young children is difficult, because personal samplers are often too heavy, bulky or impractical to be used. The Pretoddler Inhalable Particulate Environmental Robotic (PIPER) sampler was developed to help address this problem. In this study, we measured inhalable PM exposures in 2-year-olds via a lightweight personal sampler worn in a small backpack and evaluated the use of a robotic sampler with an identical sampling train for estimating PM exposure in this age group. PM mass concentrations measured by the personal sampler ranged from 100 to almost 1,200 μg/m 3 , with a median value of 331 μg/m 3 . PM concentrations measured by PIPER were considerably lower, ranging from 14 to 513 μg/m 3 with a median value of 56 μg/m 3 . Floor cleaning habits and activity patterns of the 2-year-olds varied widely by home; vigorous play and recent floor cleaning were most associated with higher personal exposure. Our findings highlight the need for additional characterization of children's activity patterns and their effect on personal exposures.

ANALYSIS OF PARTICULATE ORGANIC MATTER IN HOLOCENE SEDIMENTS OF COASTAL PLAIN FROM PERO BEACH, CABO FRIO, RIO DE JANEIRO, BRAZIL

Directory of Open Access Journals (Sweden)

Taísa Camila Silveira de Souza

2016-06-01

Full Text Available The study of palynofacies along a core drilled on the coastal plain of Cabo Frio, State of Rio de Janeiro, was carried out in order to contribute to the knowledge of the paleoenvironmental evolution of the Pero Beach region. The ages obtained from 14C datings allowed to verify that the studied core records the past 6761 ± 130 yrs cal BP. Thirty samples were prepared by standard methodology for palynofacies. About three hundred particles of the particulate organic material was classified and recorded for each sample. Statistical methods were employed for the associations of particulate organic matter (R-mode cluster analysis and levels (samples; Q-mode cluster analysis analyzed along the core. Furthermore, the ratio Phytoclast - Total Organic Carbon (Phy-TOC was used to verify the proximity of the source area. The three major groups of particulate organic matter found along the studied core are Phytoclasts, Amorphous Organic Matter (AOM and Palynomorphs. The samples showed in general, a predominance of phytoclasts (73.2%, followed by AOM (18.6% and Palynomorphs (8.2%. Supported by statistical analysis, it was possible to deduce that the study area evolved since the middle Holocene from a marine environment to a paleolagoon.

Efficiency of Respirator Filter Media against Diesel Particulate Matter: A Comparison Study Using Two Diesel Particulate Sources.

Science.gov (United States)

Burton, Kerrie A; Whitelaw, Jane L; Jones, Alison L; Davies, Brian

2016-07-01

Diesel engines have been a mainstay within many industries since the early 1900s. Exposure to diesel particulate matter (DPM) is a major issue in many industrial workplaces given the potential for serious health impacts to exposed workers; including the potential for lung cancer and adverse irritant and cardiovascular effects. Personal respiratory protective devices are an accepted safety measure to mitigate worker exposure against the potentially damaging health impacts of DPM. To be protective, they need to act as effective filters against carbon and other particulates. In Australia, the filtering efficiency of respiratory protective devices is determined by challenging test filter media with aerosolised sodium chloride to determine penetration at designated flow rates. The methodology outlined in AS/NZS1716 (Standards Australia International Ltd and Standards New Zealand 2012. Respiratory protective devices. Sydney/Wellington: SAI Global Limited/Standards New Zealand) does not account for the differences between characteristics of workplace contaminants like DPM and sodium chloride such as structure, composition, and particle size. This study examined filtering efficiency for three commonly used AS/NZS certified respirator filter models, challenging them with two types of diesel emissions; those from a diesel generator and a diesel engine. Penetration through the filter media of elemental carbon (EC), total carbon (TC), and total suspended particulate (TSP) was calculated. Results indicate that filtering efficiency assumed by P2 certification in Australia was achieved for two of the three respirator models for DPM generated using the small diesel generator, whilst when the larger diesel engine was used, filtering efficiency requirements were met for all three filter models. These results suggest that the testing methodology specified for certification of personal respiratory protective devices by Standards Australia may not ensure adequate protection for

PM10 source apportionment study in Pleasant Valley, Nevada

International Nuclear Information System (INIS)

Egami, R.T.; Chow, J.C.; Watson, J.G.; DeLong, T.

1990-01-01

A source apportionment study was conducted between March 18 and April 4, 1988, at Pleasant Valley, Nevada, to evaluate air pollutant concentrations to which community residents were exposed and the source contributions to those pollutants. Daily PM 10 samples were taken for chemical speciation of 40 trace elements, ions, and organic and elemental carbon. This paper reports that the objectives of this case study are: to determine the emissions source composition of the potential upwind source, a geothermal plant; to measure the ambient particulate concentration and its chemical characteristics in Pleasant Valley; and to estimate the contributions of different emissions sources to PM 10 . The study found that: particulate emissions from the geothermal cooling-tower plume consisted primarily of sulfate, ammonia, chloride, and trace elements; no significant quantities of toxic inorganic species were found in the ambient air; ambient PM 10 concentrations in Pleasant Valley were within Federal standards; and source contribution to PM 10 were approximately 60% geological material; 20% motor vehicle exhaust; and 10% cooling-tower plume

Assessment of Population Exposure to Coarse and Fine Particulate Matter in the Urban Areas of Chennai, India

Directory of Open Access Journals (Sweden)

Ramachandran Prasannavenkatesh

2015-01-01

Full Text Available Research outcomes from the epidemiological studies have found that the course (PM10 and the fine particulate matter (PM2.5 are mainly responsible for various respiratory health effects for humans. The population-weighted exposure assessment is used as a vital decision-making tool to analyze the vulnerable areas where the population is exposed to critical concentrations of pollutants. Systemic sampling was carried out at strategic locations of Chennai to estimate the various concentration levels of particulate pollution during November 2013–January 2014. The concentration of the pollutants was classified based on the World Health Organization interim target (IT guidelines. Using geospatial information systems the pollution and the high-resolution population data were interpolated to study the extent of the pollutants at the urban scale. The results show that approximately 28% of the population resides in vulnerable locations where the coarse particulate matter exceeds the prescribed standards. Alarmingly, the results of the analysis of fine particulates show that about 94% of the inhabitants live in critical areas where the concentration of the fine particulates exceeds the IT guidelines. Results based on human exposure analysis show the vulnerability is more towards the zones which are surrounded by prominent sources of pollution.

Assessment of Population Exposure to Coarse and Fine Particulate Matter in the Urban Areas of Chennai, India.

Science.gov (United States)

Prasannavenkatesh, Ramachandran; Andimuthu, Ramachandran; Kandasamy, Palanivelu; Rajadurai, Geetha; Kumar, Divya Subash; Radhapriya, Parthasarathy; Ponnusamy, Malini

2015-01-01

Research outcomes from the epidemiological studies have found that the course (PM10) and the fine particulate matter (PM2.5) are mainly responsible for various respiratory health effects for humans. The population-weighted exposure assessment is used as a vital decision-making tool to analyze the vulnerable areas where the population is exposed to critical concentrations of pollutants. Systemic sampling was carried out at strategic locations of Chennai to estimate the various concentration levels of particulate pollution during November 2013-January 2014. The concentration of the pollutants was classified based on the World Health Organization interim target (IT) guidelines. Using geospatial information systems the pollution and the high-resolution population data were interpolated to study the extent of the pollutants at the urban scale. The results show that approximately 28% of the population resides in vulnerable locations where the coarse particulate matter exceeds the prescribed standards. Alarmingly, the results of the analysis of fine particulates show that about 94% of the inhabitants live in critical areas where the concentration of the fine particulates exceeds the IT guidelines. Results based on human exposure analysis show the vulnerability is more towards the zones which are surrounded by prominent sources of pollution.

Characterization of traffic-related ambient fine particulate matter (PM2.5) in an Asian city: Environmental and health implications

Science.gov (United States)

Zhang, Zhi-Hui; Khlystov, Andrey; Norford, Leslie K.; Tan, Zhen-Kang; Balasubramanian, Rajasekhar

2017-07-01

Vehicular traffic emission is an important source of particulate pollution in most urban areas. The detailed chemical speciation of traffic-related PM2.5 (fine particles) is relatively sparse in the literature, especially in Asian cities. To fill this knowledge gap, we carried out an intensive field study in Singapore from November 2015 to February 2016. PM2.5 samples were collected concurrently at a typical roadside microenvironment and at an urban background site. A detailed chemical speciation of PM2.5 samples was conducted to gain insights into the emission characteristics of traffic-related fine aerosols. Analyses of diagnostic ratios and molecular markers of selected chemical species were explored for source attribution of different classes of chemical constituents in traffic-related PM2.5. The human health risk due to inhalation of the particulate-bound PAHs (polycyclic aromatic hydrocarbons) and toxic trace elements was estimated for both adults and children. The overall results of the study indicate that gasoline-powered vehicles make a higher contribution to traffic-related fine aerosol components such as organic carbon (OC), particle-bound PAHs and particulate ammonium than that of diesel-powered vehicles. However, both types of vehicles contribute to traffic-related EC emissions significantly. The combustion of petroleum fuels and lubricating oil make significant contributions to the emission of n-alkanes and hopanes into the urban atmosphere, respectively. The study further reveals that some toxic trace elements are emitted from non-exhaust sources and that aromatic acids represent an important component of secondary organic aerosols. The emission of toxic trace elements from non-exhaust sources is of particular concern as they could pose a higher carcinogenic risk to both adults and children than other chemical species.

Environmental pollution: quantitative analysis of particulate matter (PM{sub 10}) by SR-TXRF

Energy Technology Data Exchange (ETDEWEB)

Moreira, Silvana; Melo Junior, Ariston da Silva [Universidade Estadual de Campinas (UNICAMP), Campinas, SP (Brazil). Faculdade de Engenharia Civil, Arquitetura e Urbanismo]. E-mails: silvana@fec.unicamp.br; juniorariston@gmail.com; Zucchi, Orgheda Luiza Araujo Domingues [Universidade de Sao Paulo (USP), Ribeirao Preto, SP (Brazil). Faculdade de Ciencias Farmaceuticas]. E-mail: olzucchi@fcfrp.usp.br; Vives, Ana Elisa Sirito de [Universidade Metodista de Piracicaba (UNIMEP), Santa Barbara D' Oeste, SP (Brazil). Faculdade de Engenharia Civil, Arquitetura e Urbanismo]. E-mail: aesvives@unimep.br

2007-07-01

The atmospheric pollution is a concern in the great urban centers, due its association with man pathologies. The Campinas region is one of the most urbanized of the Sao Paulo State and an important industrial center. Thus, due to its location and importance were installed three samplers for particulate material (PM{sub 10}). One sampler was located in downtown of Campinas city, in an avenue with high vehicular flow. Another sampler was installed in the UNICAMP campus and the third one in Paulinia city, near to REPLAN. For downtown of Campinas city PM{sub 10} concentrations higher than regular air quality established by CETESB (150 {mu}g.m{sup -3}) was observed. The PM{sub 10} values for Paulinia and downtown of Campinas were higher than Barao Geraldo location. Employing SR-TXRF was possible identify and quantify 19 elements in the particulate material samples. All the measurements were performed at Synchrotron Light Source Laboratory, Campinas, SP. After statistics analysis by principal components and cluster analysis was possible to assemble the elements according emission sources. The dusty soil for coarse fraction contributed with 62%, 51% and 46% for Barao Geraldo, Paulinia and downtown of Campinas, respectively. The vehicular emission was responsible for 16% at downtown Campinas city as expected due to high vehicular flow at sampling place. The vehicular and industrial emissions contributed with 20% and 25%, respectively at Paulinia sampling site. The industrial emissions observed for Barao Geraldo and downtown of Campinas city were 27% and 33%, respectively. (author)

Speciated atmospheric mercury and its potential source in Guiyang, China

Science.gov (United States)

Fu, Xuewu; Feng, Xinbin; Qiu, Guangle; Shang, Lihai; Zhang, Hui

2011-08-01

Speciated atmospheric mercury (Hg) including gaseous elemental mercury (GEM), particulate Hg (PHg), and reactive gaseous Hg (RGM) were continuously measured at an urban site in Guiyang city, southwest China from August to December 2009. The averaged concentrations for GEM, PHg, and RGM were 9.72 ± 10.2 ng m -3, 368 ± 676 pg m -3, and 35.7 ± 43.9 pg m -3, respectively, which were all highly elevated compared to observations at urban sites in Europe and North America. GEM and PHg were characterized by similar monthly and diurnal patterns, with elevated levels in cold months and nighttime, respectively. In contrast, RGM did not exhibit clear monthly and diurnal variations. The variations of GEM, PHg, and RGM indicate the sampling site was significantly impacted by sources in the city municipal area. Sources identification implied that both residential coal burning and large point sources were responsible to the elevated GEM and PHg concentrations; whereas point sources were the major contributors to elevated RGM concentrations. Point sources played a different role in regulating GEM, PHg, and RGM concentrations. Aside from residential emissions, PHg levels was mostly affected by small-scale coal combustion boilers situated to the east of the sampling site, which were scarcely equipped or lacking particulate control devices; whereas point sources situated to the east, southeast, and southwest of the sampling played an important role on the distribution of atmospheric GEM and RGM.

Source Apportionment of the Summer Time Carbonaceous Aerosol at Nordic Rural Background Sites

Science.gov (United States)

In the present study, natural and anthropogenic sources of particulate organic carbon (OCp) and elemental carbon (EC) have been quantified based on weekly filter samples of PM10 (particles with aerodynamic diameter Nordic rural backgro...

Stratified source-sampling techniques for Monte Carlo eigenvalue analysis

International Nuclear Information System (INIS)

Mohamed, A.

1998-01-01

In 1995, at a conference on criticality safety, a special session was devoted to the Monte Carlo ''Eigenvalue of the World'' problem. Argonne presented a paper, at that session, in which the anomalies originally observed in that problem were reproduced in a much simplified model-problem configuration, and removed by a version of stratified source-sampling. In this paper, stratified source-sampling techniques are generalized and applied to three different Eigenvalue of the World configurations which take into account real-world statistical noise sources not included in the model problem, but which differ in the amount of neutronic coupling among the constituents of each configuration. It is concluded that, in Monte Carlo eigenvalue analysis of loosely-coupled arrays, the use of stratified source-sampling reduces the probability of encountering an anomalous result over that if conventional source-sampling methods are used. However, this gain in reliability is substantially less than that observed in the model-problem results

Sources for charged particles; Les sources de particules chargees

Energy Technology Data Exchange (ETDEWEB)

Arianer, J.

1997-09-01

This document is a basic course on charged particle sources for post-graduate students and thematic schools on large facilities and accelerator physics. A simple but precise description of the creation and the emission of charged particles is presented. This course relies on every year upgraded reference documents. Following relevant topics are considered: electronic emission processes, technological and practical considerations on electron guns, positron sources, production of neutral atoms, ionization, plasma and discharge, different types of positive and negative ion sources, polarized particle sources, materials for the construction of ion sources, low energy beam production and transport. (N.T.).

Nepal Ambient Monitoring and Source Testing Experiment (NAMaSTE): Emissions of particulate matter from garbage burning, wood and dung cooking fires, motorcycles and brick kilns

Science.gov (United States)

Jayarathne, T. S.; Rathnayake, C.; Stockwell, C.; Daugherty, K.; Islam, R. M.; Christian, T. J.; Bhave, P.; Praveen, P. S.; Panday, A. K.; Adhikari, S.; Rasmi, M.; Goetz, D.; DeCarlo, P. F.; Saikawa, E.; Yokelson, R. J.; Stone, E. A.

2016-12-01

The Nepal Ambient Monitoring and Source Testing Experiment (NAMASTE) field campaign targeted the in-situ characterization of widespread and under-sampled combustion sources in South Asia by determining emission factors (EF) for fine particulate matter (PM2.5), organic carbon (OC), elemental carbon, inorganic ions, trace metals, and organic species. Garbage burning had the highest EF PM2.5 among the sampled sources ranging 7-124 g kg-1, with maximum EFs for garbage burned under higher moisture conditions. Garbage burning emissions contained high concentrations of polycyclic aromatic compounds (PAHs) and heavy metals (Pb, Cd, Zn) that are associated with acute and chronic health effects. Triphenylbenzene and antimony (Sb) were unique to garbage burning are good candidates for tracing this source. Cook stove emissions varied largely by stove technology (traditional mud stove, 3-stone cooking fire, chimney stove, etc.) and biomass fuel (dung, hardwood, twigs, and mixtures thereof). Burning dung consistently emitted more PM2.5 than burning wood and contained characteristic fecal sterols and stanols. Motorcycle emissions were evaluated before and after servicing, which decreased EF PM2.5 from 8.8 g kg-1 to 0.7 g kg-1. Organic species analysis indicated that this reduction in PM2.5­ is largely due to a decrease in emission of motor oil. For brick kilns, the forced draft zig-zag kilns had higher EF PM2.5 (12-19 g kg-1) compared to clamp kilns (8-13 g kg-1) and also exhibited chemical differences. PM2.5 emitted from the zig-zag kiln were mainly OC (7%), sulfate (32%) and uncharacterized chemical components (60%), while clamp kiln emissions were dominated by OC (64%) and ammonium sulfate (36%). The quantitative emission factors developed in this study may be used for source apportionment and to update regional emission inventories.

Work place air particulate monitoring of automobile workshops for public health and safety

International Nuclear Information System (INIS)

Siddique, N.; Waheed, S.

2013-01-01

Twenty-eight pairs of coarse and fine air particulate samples were collected in front of an automotive workshop located at Tasmasipabad on Chaklala Road in Rawalpindi using a Gent sampler and polycarbonate filters. These samples were collected during the period; 7th to 27th of April 2009. The gravimetric data (PM 2.5 and PM 10 ) were obtained for these samples and were found to exceed the Pakistani standards. Black carbon (BC) was also determined using reflectance measurements and it was found that BC contributed significantly more to the fine mass than to the coarse fraction; i.e. ∼10 to ∼3 %, respectively. This is not surprising as soot is emitted by combustion processes and is usually found in the fine particulate mass. Using instrumental neutron activation analysis technique all 28 pairs of filters were analyzed for >30 elements. Major elements, in the coarse mass fraction, include Al, K, Fe, Sr, Na, and Zn implying soil as the major source while BC was found to be a higher contributor of PM 2.5 . An episode of high PM 2.5 was observed on the 18th of April 2009. Back trajectory analysis showed that the air mass originated from the Middle East where a dust storm was in progress over Iraq. (author)

Evaluation of sampling inhalable PM10 particulate matter (≤ 10 μm) using co-located high volume samplers

International Nuclear Information System (INIS)

Rajoy, R R S; Dias, J W C; Rego, E C P; Netto, A D Pereira

2015-01-01

This paper presents the results of the determination of the concentrations of atmospheric particulate matter ≤ 10 μm (PM10), collected simultaneously by six PM10 high volume samplers from two different manufacturers installed in the same location. Fifteen samples of 24 h were obtained with each equipment at a selected urban area of Rio de Janeiro city. The concentration of PM10 ranged between 10.73 and 54.04 μg m −3 . The samplers were considered comparable to each other, as the adopted methodology presented good repeatability

Understanding particulate coating microstructure development

Science.gov (United States)

Roberts, Christine Cardinal

How a dispersion of particulates suspended in a solvent dries into a solid coating often is more important to the final coating quality than even its composition. Essential properties like porosity, strength, gloss, particulate order, and concentration gradients are all determined by the way the particles come together as the coating dries. Cryogenic scanning electron microscopy (cryoSEM) is one of the most effective methods to directly visualize a drying coating during film formation. Using this method, the coating is frozen, arresting particulate motion and solidifying the sample so that it be imaged in an SEM. In this thesis, the microstructure development of particulate coatings was explored with several case studies. First, the effect of drying conditions was determined on the collapse of hollow latex particles, which are inexpensive whiteners for paint. Using cryoSEM, it was found that collapse occurs during the last stages of drying and is most likely to occur at high drying temperatures, humidity, and with low binder concentration. From these results, a theoretical model was proposed for the collapse of a hollow latex particle. CryoSEM was also used to verify a theoretical model for the particulate concentration gradients that may develop in a coating during drying for various evaporation, sedimentation and particulate diffusion rates. This work created a simple drying map that will allow others to predict the character of a drying coating based on easily calculable parameters. Finally, the effect of temperature on the coalescence and cracking of latex coatings was explored. A new drying regime for latex coatings was identified, where partial coalescence of particles does not prevent cracking. Silica was shown to be an environmentally friendly additive for preventing crack formation in this regime.

Chemical characterization of urban air particulate matter of Kuala Lumpur 2002-2004

International Nuclear Information System (INIS)

Wee Boon Siong; Ab. Khalik Bin Haji Wood

2006-01-01

Urban air particulate samples of Kuala Lumpur ambient air have been collected characterize according to fine and coarse airborne particulates. The air filters containing particulate matter were collected using GENT stack filter unit fitted with appropriate polycarbonate filters. The sampling location site (Lat: 03deg 10'30''; Long: 101deg 43'24.2'') is approximately 1 km from the Kuala Lumpur city center. All the sampling conducted from January 2002 until October 2004 was included in the analysis and results were reported. The mass loading for finest air particulate matter (PM 2.5) in Kuala Lumpur are 199±55 μg (2002), 171±53 μg (2003), and 171±61 μg (2004), respectively. The mass loading for coarse air particulate matter (PM 10) in Kuala Lumpur were 125±29 μg (2002), 134±48 μg (2003), and 137 ± 57 μg (2004), respectively. The elemental concentration of the air filters were determined using INAA technique utilizing both short and long irradiation facilities at MINT's TRIGA MKII reactor. Upon irradiation the air filters were counted at suitable counting time using HPGe gamma-ray detectors. The elements reported for this monitoring are Al, As, Br, Co, Cr, K, Lu, Mn, Na, Sb, Sc, Ti, V, and Zn. Certified reference materials were also included in the sample analysis function as quality control materials. (author)

Sources and Processes Affecting Particulate Matter Pollution over North China

Science.gov (United States)

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.

Fine Particulate Pollution and Source Apportionment in the Urban Centers for Africa, Asia and Latin America

Science.gov (United States)

Guttikunda, S. K.; Johnson, T. M.; Procee, P.

2004-12-01

Fossil fuel combustion for domestic cooking and heating, power generation, industrial processes, and motor vehicles are the primary sources of air pollution in the developing country cities. Over the past twenty years, major advances have been made in understanding the social and economic consequences of air pollution. In both industrialized and developing countries, it has been shown that air pollution from energy combustion has detrimental impacts on human health and the environment. Lack of information on the sectoral contributions to air pollution - especially fine particulates, is one of the typical constraints for an effective integrated urban air quality management program. Without such information, it is difficult, if not impossible, for decision makers to provide policy advice and make informed investment decisions related to air quality improvements in developing countries. This also raises the need for low-cost ways of determining the principal sources of fine PM for a proper planning and decision making. The project objective is to develop and verify a methodology to assess and monitor the sources of PM, using a combination of ground-based monitoring and source apportionment techniques. This presentation will focus on four general tasks: (1) Review of the science and current activities in the combined use of monitoring data and modeling for better understanding of PM pollution. (2) Review of recent advances in atmospheric source apportionment techniques (e.g., principal component analysis, organic markers, source-receptor modeling techniques). (3) Develop a general methodology to use integrated top-down and bottom-up datasets. (4) Review of a series of current case studies from Africa, Asia and Latin America and the methodologies applied to assess the air pollution and its sources.

Urban particulate matter pollution: a tale of five cities.

Science.gov (United States)

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.

Advanced Fine Particulate Characterization Methods

Energy Technology Data Exchange (ETDEWEB)

Steven Benson; Lingbu Kong; Alexander Azenkeng; Jason Laumb; Robert Jensen; Edwin Olson; Jill MacKenzie; A.M. Rokanuzzaman

2007-01-31

The characterization and control of emissions from combustion sources are of significant importance in improving local and regional air quality. Such emissions include fine particulate matter, organic carbon compounds, and NO{sub x} and SO{sub 2} gases, along with mercury and other toxic metals. This project involved four activities including Further Development of Analytical Techniques for PM{sub 10} and PM{sub 2.5} Characterization and Source Apportionment and Management, Organic Carbonaceous Particulate and Metal Speciation for Source Apportionment Studies, Quantum Modeling, and High-Potassium Carbon Production with Biomass-Coal Blending. The key accomplishments included the development of improved automated methods to characterize the inorganic and organic components particulate matter. The methods involved the use of scanning electron microscopy and x-ray microanalysis for the inorganic fraction and a combination of extractive methods combined with near-edge x-ray absorption fine structure to characterize the organic fraction. These methods have direction application for source apportionment studies of PM because they provide detailed inorganic analysis along with total organic and elemental carbon (OC/EC) quantification. Quantum modeling using density functional theory (DFT) calculations was used to further elucidate a recently developed mechanistic model for mercury speciation in coal combustion systems and interactions on activated carbon. Reaction energies, enthalpies, free energies and binding energies of Hg species to the prototype molecules were derived from the data obtained in these calculations. Bimolecular rate constants for the various elementary steps in the mechanism have been estimated using the hard-sphere collision theory approximation, and the results seem to indicate that extremely fast kinetics could be involved in these surface reactions. Activated carbon was produced from a blend of lignite coal from the Center Mine in North Dakota and

Proton-induced X-ray emission analysis of marine particulates

International Nuclear Information System (INIS)

Burnett, W.C.; Mitchum, G.T.

1981-01-01

We report a methodology used to analyze suspended marine particulates by particle induced X-ray emission (PIXE). Water samples from an estuary in Brazil were filtered soon after collection onto pre-weighed Nuclepore filters, washed with deionized water, dried to constant weight and analyzed as thin targets. Because of the relatively high mass loadings (0.1-1.0 mg/cm 2 ) on the filters, proton bombardment times of a few minutes were adequate for maintaining good counting statistics. Precision and accuary were determined by replicate analysis and intercomparison to geochemical standards. Suspensions of standards in deionized water were filtered dried, weighed and analyzed in a similar fashion as our samples of marine particulates. Net X-ray intensities were related to mass by calibration against pure elemental standards. Initial experiments showed systematically low concentrations for all elements determined by PIXE relative to known values. Further experiments verified that this systematic errors was due to an uneven distribution of mass on the surface of the filters. Improvements in the filtration technique have eliminated the topographic effect on our samples and the PIXE resultes were substantially improved. Variations in matrix and particle size of the samples analyzed did not cause any measureable analytical effect. PIXE thus seems well suited for providing rapid, multi-element data on samples of marine particulates if suitable precautions are made during the sample preparation process. (orig.)

Iron persistence in a distal hydrothermal plume supported by dissolved-particulate exchange

Science.gov (United States)

Fitzsimmons, Jessica N.; John, Seth G.; Marsay, Christopher M.; Hoffman, Colleen L.; Nicholas, Sarah L.; Toner, Brandy M.; German, Christopher R.; Sherrell, Robert M.

2017-02-01

Hydrothermally sourced dissolved metals have been recorded in all ocean basins. In the oceans' largest known hydrothermal plume, extending westwards across the Pacific from the Southern East Pacific Rise, dissolved iron and manganese were shown by the GEOTRACES program to be transported halfway across the Pacific. Here, we report that particulate iron and manganese in the same plume also exceed background concentrations, even 4,000 km from the vent source. Both dissolved and particulate iron deepen by more than 350 m relative to 3He--a non-reactive tracer of hydrothermal input--crossing isopycnals. Manganese shows no similar descent. Individual plume particle analyses indicate that particulate iron occurs within low-density organic matrices, consistent with its slow sinking rate of 5-10 m yr-1. Chemical speciation and isotopic composition analyses reveal that particulate iron consists of Fe(III) oxyhydroxides, whereas dissolved iron consists of nanoparticulate Fe(III) oxyhydroxides and an organically complexed iron phase. The descent of plume-dissolved iron is best explained by reversible exchange onto slowly sinking particles, probably mediated by organic compounds binding iron. We suggest that in ocean regimes with high particulate iron loadings, dissolved iron fluxes may depend on the balance between stabilization in the dissolved phase and the reversibility of exchange onto sinking particles.

Novel mass spectrometric instrument for gaseous and particulate characterization and monitoring

International Nuclear Information System (INIS)

Coggiola, M.J.

1994-02-01

SRI International will develop a unique new instrument that will be capable of providing real-time (<1 minute), quantitative, chemical characterization of gaseous and particulate pollutants generated from DOE waste cleanup activities. The instrument will be capable of detecting and identifying volatile organic compounds, polynuclear aromatic hydrocarbons, heavy metals, and transuranic species released during waste cleanup activities. The instrument will be unique in its ability to detect and quantify in real-time these diverse pollutants in both vapor and particulate form. The instrument to be developed under this program will consist of several major components: (1) an isokinetic sampler capable of operating over a wide range of temperatures (up to 500 K) and flow rates; (2) a high pressure to low pressure transition and sampling region that efficiently separates particles from vapor-phase components for separate, parallel analyses; (3) two small mass spectrometers, one optimized for organic analysis using a unique field ionization source and one optimized for particulate characterization using thermal pyrolysis and electron-impact ionization (EI); and (4) a powerful personal computer for control and data acquisition. Initially, the instrument will be developed for targeted use in conjunction with the K-1435 Toxic Substances Control Act (TSCA) incinerator at the Oak Ridge National Laboratory K-25 site. Ultimately, the instrument will be designed to operate in the field at any cleanup site, located close to the stack or process vent, providing the plant operations personnel with real-time information and alarm capabilities. In addition, this instrument will be very broadly applicable for cleanup or sampling, for example, any time contaminated soil is moved or disturbed

Study of indoor and ambient air fungual bioaerosols and its relation with particulate matters in a hospital of khorramabad

Directory of Open Access Journals (Sweden)

Hasan Basiri

2016-02-01

Full Text Available Background: The climate change and particulate matter emission contented of bioaerosols is known as an important reason of increasing the allergic interactions especially in patients with defect in immunity system. The aim of this study was to investigate fungal bioaerosol concentrations in relation to particulate matter (PM10, PM2.5 and PM1 in indoor parts and ambient air of the generd educational hospital of Khorramabad city. Materials and Methods: In this descriptive-analytical study, 192 samples (168 for indoor and 24 for outdoor were gathered during 6 months at the seven indoor wards and one outdoor unit using Quick Take-30 method  at an airflow rate of 28.3 L/min and sampling time of 2.5 min on to Sabouraud dextrose agar medium containing chloramphenicol. The sampling of particulate matter was carried out by Monitor Dust-Trak 8520. Also, the relative humidity and temperature were surveyed by TES-1360 digital. Results: The results showed that infectious ward with 101.7 CFU/m3 was as the most contaminated part and operating room with 46.4 CFU/m3 was the cleanest part. Cladosporium with 36.75% and Rodotorolla with 1.3% had higher and lower of fungi rates, respectively. The rate of  I/O<1  illustrate that this contamination had an outdoor source. Conclusion: The surveys demonstrated that the increase of temperature and relative humidity have an effective influence on the pollutant accumulation. In addition, between fungi bioaerosols frequency and particulate matter ther was a significant correlation.

New Insights from Zinc and Copper Isotopic Compositions into the Sources of Atmospheric Particulate Matter from Two Major European Cities.

Science.gov (United States)

Gonzalez, R Ochoa; Strekopytov, S; Amato, F; Querol, X; Reche, C; Weiss, D

2016-09-20

This study reports spatial and temporal variability of Zn and Cu isotopes in atmospheric particulate matter (PM) collected in two major European cities with contrasting atmospheric pollution, Barcelona and London. We demonstrate that nontraditional stable isotopes identify source contributions of Zn and Cu and can play a major role in future air quality studies. In Barcelona, samples of fine PM were collected at street level at sites with variable traffic density. The isotopic signatures ranged between -0.13 ± 0.09 and -0.51 ± 0.05‰ for δ(66)ZnIRMM and between +0.04 ± 0.20 and +0.33 ± 0.15‰ for δ(65)CuAE633. Copper isotope signatures similar to those of Cu sulfides and Cu/Sb ratios within the range typically found in brake wear suggest that nonexhaust emissions from vehicles are dominant. Negative Zn isotopic signatures characteristic for gaseous emissions from smelting and combustion and large enrichments of Zn and Cd suggest contribution from metallurgical industries. In London, samples of coarse PM collected on the top of a building over 18 months display isotope signatures ranging between +0.03 ± 0.04 and +0.49 ± 0.02‰ for δ(66)ZnIRMM and between +0.37 ± 0.17 and +0.97 ± 0.21‰ for δ(65)CuAE633. Heavy Cu isotope signatures (up to +0.97 ± 0.21‰) and higher enrichments and Cu/Sb ratios during winter time indicate important contribution from fossil fuel combustion. The positive δ(66)ZnIRMM signatures are in good agreement with signatures characteristic for ore concentrates used for the production of tires and galvanized materials, suggesting nonexhaust emissions from vehicles as the main source of Zn pollution.

Effect of sample digestion, air filter contamination, and post-adsorption on the analysis of trace elements in air particulate matter

International Nuclear Information System (INIS)

Yang, Xiao Jin; Wan, Pingyu; Foley, Roy

2012-01-01

Inductively coupled plasma atomic emission spectrometry and inductively coupled plasma MS are the major analytical tools for trace elements in environmental matrices, however, the underestimate of certain trace elements in analysis of air particulate matter by these two techniques has long been observed. This has been attributed to incomplete sample digestion. Here, we demonstrate that the combined effects of sample digestion, air filter impurities, and post-adsorption of the analytes contribute to the interference of the analysis. Particular attention should be paid to post-adsorption of analytes onto air filters after acid digestion. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Effect of sample digestion, air filter contamination, and post-adsorption on the analysis of trace elements in air particulate matter

Energy Technology Data Exchange (ETDEWEB)

Yang, Xiao Jin [Department of Environment and Climate Change, Environmental Forensic and Analytical Science Section, New South Wales (Australia); Department of Applied Chemistry, College of Chemical Engineering, Beijing University of Chemical Technology, Beijing (China); Wan, Pingyu [Department of Applied Chemistry, College of Chemical Engineering, Beijing University of Chemical Technology, Beijing (China); Foley, Roy [Department of Environment and Climate Change, Environmental Forensic and Analytical Science Section, New South Wales (Australia)

2012-11-15

Inductively coupled plasma atomic emission spectrometry and inductively coupled plasma MS are the major analytical tools for trace elements in environmental matrices, however, the underestimate of certain trace elements in analysis of air particulate matter by these two techniques has long been observed. This has been attributed to incomplete sample digestion. Here, we demonstrate that the combined effects of sample digestion, air filter impurities, and post-adsorption of the analytes contribute to the interference of the analysis. Particular attention should be paid to post-adsorption of analytes onto air filters after acid digestion. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Analysis of aliphatic and aromatic hydrocarbons in particulate matter in Madrid urban area

International Nuclear Information System (INIS)

Perez, M.; Mendez, J.; Bomboi, M.T.

1988-01-01

Levels of n-alkanes and polycyclic aromatic hydrocarbons have been measured in the air particulate matter during six months, from January to June of 1987, in an urban area of Madrid. The hydrocarbons were collected on glass fiber filters by high volumen sampling. The extraction was carried out by Sohxlet and ultrasonic techniques. The extracts were clean-up on silicagel fractionation and the chromatographic analysis was performed by capillary column gas chromatographic. Final results are discussed as well as the immission values related to the possible emission sources. (Author)

Airborne particulate matter collection and analysis by XRF

International Nuclear Information System (INIS)

Santos, Flora L.; Esguerra, Luz V.; Pabroa, Preciosa B.; Almoneda, Rosalina

2004-01-01

The Philippine Nuclear Research Institute (PNRI) continues to pursue its air pollution research in support of the implementation of the 1999 Clean Air Act. The primary tool for analysis is X-Ray Fluorescence spectrometry (XRF) since the PPP-I is still on extended shut down. Following the workplan approved during the 1991 Workshop on Utilization of Research Reactors, the PNRI collected airborne particulate matter using the Gent sampler. The sampling site selected for the program was Poveda Learning Center, located beside a major highway, the Epifanio delos Santos Avenue (EDSA) where the principal source of pollution is vehicular emissions. Samples collected up to August were analyzed by XRF using three sets of analytical parameters to allow optimized analysis of a wider range of elements including Na and Pb. Although the PNRI has no operating reactor, it has personnel who have trained in NAA but are unable to apply the technique. As mentioned in the 2001 Workshop, the PNRI is considering several options to resume reactor-related activities. Thus, it is necessary to ensure continuing availability of expertise in NAA in the PNRI. It looks forward to collaborating with other Institutes through the FNCA program for the analysis of samples by NAA and using reactor parameters from collaborating Institute, to obtain experience in the use of Ko. This would also allow validation of XRF data obtained for these samples. In return it can analyze samples for collaborating institutions to generate data on Pb and S, which are important for pollutant source apportionment. (author)

[Characteristics and sources of particulate polycyclic aromatic hydrocarbons (PAHs) during haze period in Guangzhou].

Science.gov (United States)

Duan, Jing-Chun; Tan, Ji-Hua; Sheng, Guo-Ying; Fu, Jia-Mo

2009-06-15

PM10 (particulates matter with aerodynamic diameter Guangzhou city between March 2002 and June 2003. Polycyclic aromatic hydrocarbons (PAHs) were studied during haze and non-haze periods in both summer and winter. PAHs pollution was serious in haze period compared with that in non-haze period, especially in winter. Compared with non-haze period, Phe, Ant, Flu, Pyr, BaA, Chr, IcdP, DahA and BghiP were more abundant in haze period in summer, and BaF, BeP, BaP, Pery, IcdP, DahA and BghiP were more abundant in haze period in winter. The BEQ values were 3.5 ng x m(-3), 3.35 ng x m(-3), 1.43 ng x m(-3) and 13.0 ng x m(-3) in non-haze in summer, in haze in summer, in non-haze in winter and in haze in winter, respectively. The BEQ values in non-haze in summer, in haze in summer and in non-haze in winter in Guangzhou (average: 2.76 ng x m(-3)) were relatively low in Chinese cities, and comparable with oversea cities. However, the BEQ value in haze in winter was relatively high in Chinese cities. It indicated that haze in winter would impair human health seriously. The diagnostic ratios suggested gasoline and diesel vehicle emission were main sources of PAHs in summer, and diesel vehicle and coal combustion emission were main sources of PAHs in winter; PAHs may come from both local sources and long-range transportation in non-haze in winter.

Honey Bees (Apis mellifera, L.) as Active Samplers of Airborne Particulate Matter.

Science.gov (United States)

Negri, Ilaria; Mavris, Christian; Di Prisco, Gennaro; Caprio, Emilio; Pellecchia, Marco

2015-01-01

Honey bees (Apis mellifera L.) are bioindicators of environmental pollution levels. During their wide-ranging foraging activity, these hymenopterans are exposed to pollutants, thus becoming a useful tool to trace the environmental contaminants as heavy metals, pesticides, radionuclides and volatile organic compounds. In the present work we demonstrate that bees can also be used as active samplers of airborne particulate matter. Worker bees were collected from hives located in a polluted postmining area in South West Sardinia (Italy) that is also exposed to dust emissions from industrial plants. The area is included in an official list of sites of national interest for environmental remediation, and has been characterized for the effects of pollutants on the health of the resident population. The head, wings, hind legs and alimentary canal of the bees were investigated with Scanning Electron Microscopy coupled with X-ray spectroscopy (SEM-EDX). The analyses pointed to specific morphological and chemical features of the particulate, and resulted into the identification of three categories of particles: industry-, postmining-, and soil-derived. With the exception of the gut, all the analyzed body districts displayed inorganic particles, mostly concentrated in specific areas of the body (i.e. along the costal margin of the fore wings, the medial plane of the head, and the inner surface of the hind legs). The role of both past mining activities and the industrial activity close to the study area as sources of the particulate matter is also discussed. We conclude that honey bees are able to collect samples of the main airborne particles emitted from different sources, therefore could be an ideal tool for monitoring such a kind of pollutants.

Assessment of diesel particulate matter exposure in the workplace: freight terminals†

Science.gov (United States)

Sheesley, Rebecca J.; Schauer, James J.; Smith, Thomas J.; Garshick, Eric; Laden, Francine; Marr, Linsey C.; Molina, Luisa T.

2008-01-01

A large study has been undertaken to assess the exposure to diesel exhaust within diesel trucking terminals. A critical component of this assessment is an analysis of the variation in carbonaceous particulate matter (PM) across trucking terminal locations; consistency in the primary sources can be effectively tracked by analyzing trends in elemental carbon (EC) and organic molecular marker concentrations. Ambient samples were collected at yard, dock and repair shop work stations in 7 terminals in the USA and 1 in Mexico. Concentrations of EC ranged from 0.2 to 12 μg m−3 among the terminals, which corresponds to the range seen in the concentration of summed hopanes (0.5 to 20.5 ng m−3). However, when chemical mass balance (CMB) source apportionment results were presented as percent contribution to organic carbon (OC) concentrations, the contribution of mobile sources to OC are similar among the terminals in different cities. The average mobile source percent contribution to OC was 75.3 ± 17.1% for truck repair shops, 65.4 ± 20.4% for the docks and 38.4 ± 9.5% for the terminal yard samples. A relatively consistent mobile source impact was present at all the terminals only when considering percentage of total OC concentrations, not in terms of absolute concentrations. PMID:18392272

Source apportionment of airborne particulate matter using organic compounds as tracers

Science.gov (United States)

Schauer, James J.; Rogge, Wolfgang F.; Hildemann, Lynn M.; Mazurek, Monica A.; Cass, Glen R.; Simoneit, Bernd R. T.

A chemical mass balance receptor model based on organic compounds has been developed that relates source contributions to airborne fine particle mass concentrations. Source contributions to the concentrations of specific organic compounds are revealed as well. The model is applied to four air quality monitoring sites in southern California using atmospheric organic compound concentration data and source test data collected specifically for the purpose of testing this model. The contributions of up to nine primary particle source types can be separately identified in ambient samples based on this method, and approximately 85% of the organic fine aerosol is assigned to primary sources on an annual average basis. The model provides information on source contributions to fine mass concentrations, fine organic aerosol concentrations and individual organic compound concentrations. The largest primary source contributors to fine particle mass concentrations in Los Angeles are found to include diesel engine exhaust, paved road dust, gasoline-powered vehicle exhaust, plus emissions from food cooking and wood smoke, with smaller contribution from tire dust, plant fragments, natural gas combustion aerosol, and cigarette smoke. Once these primary aerosol source contributions are added to the secondary sulfates, nitrates and organics present, virtually all of the annual average fine particle mass at Los Angeles area monitoring sites can be assigned to its source.

A persisting secondhand smoke hazard in urban public places: results from fine particulate (PM2.5) air sampling.

Science.gov (United States)

Wilson, Nick; Edwards, Richard; Parry, Rhys

2011-03-04

To assess the need for additional smokefree settings, by measuring secondhand smoke (SHS) in a range of public places in an urban setting. Measurements were made in Wellington City during the 6-year period after the implementation of legislation that made indoor areas of restaurants and bars/pubs smokefree in December 2004, and up to 20 years after the 1990 legislation making most indoor workplaces smokefree. Fine particulate levels (PM2.5) were measured with a portable real-time airborne particle monitor. We collated data from our previously published work involving random sampling, purposeful sampling and convenience sampling of a wide range of settings (in 2006) and from additional sampling of selected indoor and outdoor areas (in 2007-2008 and 2010). The "outdoor" smoking areas of hospitality venues had the highest particulate levels, with a mean value of 72 mcg/m3 (range of maximum values 51-284 mcg/m3) (n=20 sampling periods). These levels are likely to create health hazards for some workers and patrons (i.e., when considered in relation to the WHO air quality guidelines). National survey data also indicate that these venues are the ones where SHS exposure is most frequently reported by non-smokers. Areas inside bars that were adjacent to "outdoor" smoking areas also had high levels, with a mean of 54 mcg/m3 (range of maximum values: 18-239 mcg/m3, for n=13 measurements). In all other settings mean levels were lower (means: 2-22 mcg/m3). These other settings included inside traditional style pubs/sports bars (n=10), bars (n=18), restaurants (n=9), cafes (n=5), inside public buildings (n=15), inside transportation settings (n=15), and various outdoor street/park settings (n=22). During the data collection in all settings made smokefree by law, there was only one occasion of a person observed smoking. The results suggest that compliance in pubs/bars and restaurants has remained extremely high in this city in the nearly six years since implementation of the

Sources, transformation and fate of particulate amino acids and hexosamines under varying hydrological regimes in the tropical Wenchang/Wenjiao Rivers and Estuary, Hainan, China

Science.gov (United States)

Unger, Daniela; Herbeck, Lucia S.; Li, Min; Bao, Hongyan; Wu, Ying; Zhang, Jing; Jennerjahn, Tim

2013-04-01

The small tropical Wenchang and Wenjiao Rivers on the island of Hainan, tropical China, are affected by effluents from municipal sewage, aquaculture and agriculture, and by contrasting hydrological regimes related to monsoon and tropical storms. In order to obtain information on the sources, transformation and fate of organic matter (OM) we investigated the amount and composition of amino acids and hexosamines as well as the carbon isotope composition in suspended particulate matter (SPM) from the Wenchang/Wenjiao Estuary. SPM was collected along the salinity gradient starting from the river sites, along the lagoon-shaped Bamen Bay to coastal waters during four sampling campaigns between 2006 and 2009. SPM concentrations ranged between 4.7 and 58.2 mg L-1. Apart from highest values after heavy rain events in spring and summer, SPM showed little seasonal variation, but increased with salinity. From SPM POC% (1.2-20.9%), C/N (4.9-16.5) and δ13Corg (-31.5 to -19.5‰), the molar composition and content of amino acids and hexosamines (8.2-156.2 mg g-1 dry weight) and by comparison with sediments, mangroves, soils and plants we are able to show that soil-derived material, freshwater and marine plankton were the major sources of suspended OM. High POC and amino acid contents were related to primary production sustained by dissolved nutrients to a large extent stemming from municipal and aquaculture effluents. Factor analysis showed that the suite of biogeochemical parameters measured clearly depict the terrestrial vs. marine origin and the freshness/reactivity of OM. The four groups of samples resulting from cluster analysis were basically related to varying hydrological regimes. With respect to the sources, degradation and fate of particulate OM the major factors were: (i) the year round input of labile, amino acid rich riverine OM matter at the freshwater dominated sites, (ii) high input of degraded soil OM after heavy rains with dispersal throughout the estuary and

Some aspects of organic and inorganic particulate transport at Rocky Flats. Final report

International Nuclear Information System (INIS)

Nichols, H.

Findings from the summer 1975 sampling program and the conclusions from the 1975-1976 winter sampling program are summarized. Large radionuclide particles were not found attached to pollen. Sampling the airborne pollen throughout the Rocky Flats area demonstrated that the Rocky Flats air samplers were deficient in their abilities to properly collect large lightweight pollen grains. This may not have serious consequences for the undetected transport of radionuclides by pollen, however, it has implications of sampling inefficiency in some particulate size ranges, and implies that if radionuclides are carried at times by larger particles, then the standard Rocky Flats air samplers are not sampling these materials efficiently. Some initial findings suggested that soil samples from downwind areas associated with winter snow accumulation had abnormally high fissile particle accumulations, and this suggested the need to sample these sites in winter. Areas of preferred particle accumulation such as snow banks had higher concentrations of radionuclide particles than surrounding areas which are more windswept. Any soil sampling program at Rocky Flats which seeks to monitor background radionuclide levels and movement of fissile particles across the site should take account of these topographically and wind-controlled accumulation areas, and not rely solely on a grid pattern of sampling. The snow samples contained radionuclide material in substantial quantities. In terms of fissile particulates smaller than 0.5 microns the snow banks three miles east of the plant site contained as much or more radionuclides than sites close to the Hot Spot contaminated area. The snow samples immediately east of the Hot Spot contained many more large particles (>0.5 m), as did soil samples from the upwind site next to the plant fence. The Hot Spot is clearly implicated again as the source of these materials

Characteristics, Causes, and Evaluation of Helicopter Particulate Visual Obstruction

Science.gov (United States)

2012-09-10

future full-scale testing. The thrust sources examined were a 1 in. diameter nozzle , a 4 in. diameter nozzle , and a 16 in. ducted fan. The sources...Hiller also evaluated inclining the thrust vector , and determined there was little reduction in dynamic pressure at the point of ground interaction...CHARACTERISTICS, CAUSES, AND EVALUATION OF HELICOPTER PARTICULATE VISUAL OBSTRUCTION THESIS

Particulate and soluble 210Pd activities in the deep sea

International Nuclear Information System (INIS)

Somayajulu, B.L.K.; Craig, H.

1976-01-01

Particulate and soluble, 210 Pb activities have been measured by filtration of large-volume water samples at two stations in the South Atlantic. Particulate phase 210 Pb (caught by a 0.4-μm filter) varies from 0.3% of total 210 Pb in equatorial surface water to 15% in the bottom water. The 'absolute activity' of 210 Pb per unit mass of particulate matter is about 10 7 times the activity of soluble 210 Pb per unit mass of water, but because the mass ratio of particulate matter to water is about 10 -8 , the particulate phase carries only about 10% of the total activity. In Antarctic surface water the particulate phase carries 40% of the total 210 Pb activity; the absolute activity of this material is about the same as in other water masses and the higher fraction is due to the much larger concentration of suspended matter in surface water in this region. In the equatorial Atlantic the particulate phase 210 Pb activity increases with depth, by a factor of 40 from surface to bottom, and by a factor of 4 from the Antarctic Intermediate water core to the Antarctic Bottom Water. (Auth.)

Gaseous and particulate emissions from prescribed burning in Georgia.

Science.gov (United States)

Lee, Sangil; Baumann, Karsten; Schauer, James J; Sheesley, Rebecca J; Naeher, Luke P; Meinardi, Simone; Blake, Donald R; Edgerton, Eric S; Russell, Armistead G; Clements, Mark

2005-12-01

Prescribed burning is a significant source of fine particulate matter (PM2.5) in the southeastern United States. However, limited data exist on the emission characteristics from this source. Various organic and inorganic compounds both in the gas and particle phase were measured in the emissions of prescribed burnings conducted at two pine-dominated forest areas in Georgia. The measurements of volatile organic compounds (VOCs) and PM2.5 allowed the determination of emission factors for the flaming and smoldering stages of prescribed burnings. The VOC emission factors from smoldering were distinctly higher than those from flaming except for ethene, ethyne, and organic nitrate compounds. VOC emission factors show that emissions of certain aromatic compounds and terpenes such as alpha and beta-pinenes, which are important precursors for secondary organic aerosol (SOA), are much higher from active prescribed burnings than from fireplace wood and laboratory open burning studies. Levoglucosan is the major particulate organic compound (POC) emitted for all these studies, though its emission relative to total organic carbon (mg/g OC) differs significantly. Furthermore, cholesterol, an important fingerprint for meat cooking, was observed only in our in situ study indicating a significant release from the soil and soil organisms during open burning. Source apportionment of ambient primary fine particulate OC measured at two urban receptor locations 20-25 km downwind yields 74 +/- 11% during and immediately after the burns using our new in situ profile. In comparison with the previous source profile from laboratory simulations, however, this OC contribution is on average 27 +/- 5% lower.

Observations on particulate organic nitrates and unidentified components of NOy

DEFF Research Database (Denmark)

Nielsen, T.; Egeløv, A.H.; Granby, K.

1995-01-01

A method to determine the total content of particulate organic nitrates (PON) has been developed and ambient air measurements of PON, NO, NO2, HNO3, peroxyacetyl nitrate (PAN), peroxypropionyl nitrate (PPN), gas NOy and particulate inorganic nitrate have been performed in the spring and early...... summer al an agricultural site in Denmark and compared with measurements of ozone, H2O2, SO2, formic acid, acetic acid and methane sulphonic acid. The gas NOy detector determines the sum NO + NO2 + HNO2 + HNO3 + PAN + PPN + gas phase organic nitrates + 2 x N2O5 + NO3. The content of residual gas NOy...... = gas NOy + particulate inorganic nitrate). Residual gas NOy was much higher than the particulate fraction of organic nitrates (PON). PON was only 0.25 +/- 0.11% of concentrations of photochemical oxidants in connection with high-pressure systems suggesting atmospheric processes being the major source...

Characterization and source apportionment of fine particulate sources at Rijeka, Croatia from 2013 to 2015

International Nuclear Information System (INIS)

Ivošević, Tatjana; Stelcer, Eduard; Orlić, Ivica; Bogdanović Radović, Iva; Cohen, David

2016-01-01

PM_2_._5 daily aerosol samples were collected in Rijeka, Croatia during period from 6th August 2013 to 29th January 2015. In total, 259 samples were collected on Teflon filters and analyzed by PIXE and PIGE techniques to give information on 21 elements from Na to Pb. Additionally, black carbon was determined with the Laser Integrated Plate Method. Results were statistically evaluated using Positive Matrix Factorization (PMF). Eight major pollution sources: auto, smoke, secondary sulfates, heavy oil combustion, sea spray, road dust, industry iron and soil dust were identified together with their relative contributions in total PM_2_._5 pollution.

Effect of lubricant oil properties on the performance of gasoline particulate filter (GPF)

Energy Technology Data Exchange (ETDEWEB)

Shao, Huifang; Lam, William; Remias, Joseph; Roos, Joseph; Seong, HeeJe; Choi, Seungmok

2016-10-17

Mobile source emissions standards are becoming more stringent and particulate emissions from gasoline direct injection (GDI) engines represent a particular challenge. Gasoline particulate filter (GPF) is deemed as one possible technical solution for particulate emissions reduction. In this work, a study was conducted on eight formulations of lubricants to determine their effect on GDI engine particulate emissions and GPF performance. Accelerated ash loading tests were conducted on a 2.4L GDI engine with engine oil injection in gasoline fuel by 2%. The matrix of eight formulations was designed with changing levels of sulfated ash (SASH) level, Zinc dialkyldithiophosphates (ZDDP) level and detergent type. Comprehensive evaluations of particulates included mass, number, size distribution, composition, morphology and soot oxidation properties. GPF performance was assessed through filtration efficiency, back pressure and morphology. It was determined that oil formulation affects the particulate emission characteristics and subsequent GPF performance.

Evaluation of airborne particulates and fungi during hospital renovation.

Science.gov (United States)

Overberger, P A; Wadowsky, R M; Schaper, M M

1995-07-01

This study was conducted over 30 weeks on a hospital floor undergoing partial renovation. Some patients housed on the floor were immunosuppressed, including bone marrow transplant recipients. The construction zone was placed under negative pressure and was separated from patient rooms by existing hospital walls and via erection of a temporary barrier. Other control measures minimized patient exposure to airborne materials. Air sampling was done for 3 weeks prior to construction, 24 weeks during construction, and 3 weeks after renovation was completed. Airborne particulate concentrations, total spore counts, particle size, and fungal species were assessed. At the beginning of the renovation there were increases in airborne particulates (from 0.2 to 2.0 mg/m3) and fungal spores (from 3.5 to 350 colony forming units (CFU/m3), but only in the construction zone. Throughout the remainder of the renovation, particulate and fungal spore levels fluctuated inside the construction zone but remained close to baseline values in the patient area. When renovation was completed, particulates and spore counts inside the construction zone decreased to preconstruction levels. The primary fungus isolated from air samples was Penicillium. This study demonstrated that control measures were effective in reducing exposures of hospitalized patients to airborne particulates and spores and in reducing the increased risk of aspergillosis and other fungal infections associated with hospital construction projects. The data from this study may be useful in establishing exposure guidelines for other health care settings.

Day and night variation in chemical composition and toxicological responses of size segregated urban air PM samples in a high air pollution situation

Science.gov (United States)

Jalava, P. I.; Wang, Q.; Kuuspalo, K.; Ruusunen, J.; Hao, L.; Fang, D.; Väisänen, O.; Ruuskanen, A.; Sippula, O.; Happo, M. S.; Uski, O.; Kasurinen, S.; Torvela, T.; Koponen, H.; Lehtinen, K. E. J.; Komppula, M.; Gu, C.; Jokiniemi, J.; Hirvonen, M.-R.

2015-11-01

Urban air particulate pollution is a known cause for adverse human health effects worldwide. China has encountered air quality problems in recent years due to rapid industrialization. Toxicological effects induced by particulate air pollution vary with particle sizes and season. However, it is not known how distinctively different photochemical activity and different emission sources during the day and the night affect the chemical composition of the PM size ranges and subsequently how it is reflected to the toxicological properties of the PM exposures. The particulate matter (PM) samples were collected in four different size ranges (PM10-2.5; PM2.5-1; PM1-0.2 and PM0.2) with a high volume cascade impactor. The PM samples were extracted with methanol, dried and thereafter used in the chemical and toxicological analyses. RAW264.7 macrophages were exposed to the particulate samples in four different doses for 24 h. Cytotoxicity, inflammatory parameters, cell cycle and genotoxicity were measured after exposure of the cells to particulate samples. Particles were characterized for their chemical composition, including ions, element and PAH compounds, and transmission electron microscopy (TEM) was used to take images of the PM samples. Chemical composition and the induced toxicological responses of the size segregated PM samples showed considerable size dependent differences as well as day to night variation. The PM10-2.5 and the PM0.2 samples had the highest inflammatory potency among the size ranges. Instead, almost all the PM samples were equally cytotoxic and only minor differences were seen in genotoxicity and cell cycle effects. Overall, the PM0.2 samples had the highest toxic potential among the different size ranges in many parameters. PAH compounds in the samples and were generally more abundant during the night than the day, indicating possible photo-oxidation of the PAH compounds due to solar radiation. This was reflected to different toxicity in the PM

A Multi-Sample Cs-Sputter Negative Ion Source

International Nuclear Information System (INIS)

Alton, G.D.; Ball, J.A.; Bao, Y.; Cui, B.; Reed, C.A.; Williams, C.

1998-01-01

A multi-sample Cs sputter negative-ion source, equipped with a conical-geometry, W-surface-ionizer has been designed and fabricated that permits sample changes without disruption of on-line accelerator operation. Sample changing is effected by actuating an electro-pneumatic control system located at ground potential that drives an air-motor-driven sample-indexing-system mounted at high voltage; this arrangement avoids complications associated with indexing mechanisms that rely on electronic power-supplies located at high potential. In-beam targets are identified by LED indicator lights derived from a fiber-optic, Gray-code target-position sensor. Aspects of the overall source design and details of the indexing mechanism along with operational parameters, ion optics. intensities, and typical emittances for a variety of negative-ion species will be presented in this report

A Multi-Sample Cs-Sputter Negative Ion Source

Energy Technology Data Exchange (ETDEWEB)

Alton, G.D.; Ball, J.A.; Bao, Y.; Cui, B.; Reed, C.A.; Williams, C.

1998-10-05

A multi-sample Cs sputter negative-ion source, equipped with a conical-geometry, W-surface-ionizer has been designed and fabricated that permits sample changes without disruption of on-line accelerator operation. Sample changing is effected by actuating an electro-pneumatic control system located at ground potential that drives an air-motor-driven sample-indexing-system mounted at high voltage; this arrangement avoids complications associated with indexing mechanisms that rely on electronic power-supplies located at high potential. In-beam targets are identified by LED indicator lights derived from a fiber-optic, Gray-code target-position sensor. Aspects of the overall source design and details of the indexing mechanism along with operational parameters, ion optics. intensities, and typical emittances for a variety of negative-ion species will be presented in this report.

Nickel and vanadium in air particulates at Dhahran (Saudi Arabia) during and after the Kuwait oil fires

Science.gov (United States)

Sadiq, M.; Mian, A. A.

Air particulates, both the total suspended (TSP) and inhalable (PM 10, smaller than 10 microns in size), were collected during and after the Kuwait oil fires (from March 1991 to July 1992) using Hi-Vol samplers. These samples were wet-digested at 120°C in an aqua regia and perchloric acids mixture for 3 h. Air particulate samples collected in 1982 at the same location were prepared similarly. Concentrations of nickel and vanadium were determined in the aliquot samples using an inductively coupled argon plasma analyser (ICAP). The monthly mean concentrations of nickel and vanadium, on volume basis, increased rapidly from March to June and decreased sharply during July-August in 1991. The minimum mean concentrations of these elements were found in the particulate samples collected in December 1991 which gradually increased through May 1992. Like 1991, nickel and vanadium concentrations in the air particulates spiked in June and decreased again in July 1992. This distribution pattern of nickel and vanadium concentrations was similar to that of the predominant wind from the north (Kuwait). In general, concentrations of these elements were higher in the air particulates collected during April-July 1991 as compared with those collected in 1992 during the same period. The TSPs contained higher concentrations of nickel and vanadium than those found in the PM 10 samples. However, this trend was reversed when concentrations of nickel and vanadium, on were expressed on particulate weight basis. The monthly mean concentrations of nickel and vanadium, on weight basis, decreased gradually through 1991 and increased slightly from March to July 1992. Concentrations of these elements were significantly higher in the air particulate samples collected in 1991 than those samples collected during 1982 at the same location. The data of this study suggest a contribution of the Kuwait oil fires in elevating nickel and vanadium concentrations in the air particulates at Dhahran during

Ambient air particulate matter in Lagos, Nigeria: a study using receptor modeling with x-ray flourescence analysis

Directory of Open Access Journals (Sweden)

E.A. Oluyemi

2001-12-01

Full Text Available The need for comprehensive air pollution studies in Lagos cannot be overemphasized in view of the level of industrialization of the city and its nearness to the ocean. Air particulate samples collected with a high-volume air sampler at three locations in Lagos, Nigeria were analyzed by the combination of wavelength-dispersive X-ray fluorescence and atomic absorption spectroscopy methods. Elemental concentrations were subjected to factor analysis for source identification and chemical mass balance model was used for source apportionment. Prominent among sources identified with the ranges of their contributions at the sites are: soil 35-54%, marine 26-34%, automobile exhaust 0.3-3.5%, refuse incineration 2-3%, and regional sulphate 2-12%.

Evaluation of particulate filtration efficiency of retrofit particulate filters for light duty vehicles

International Nuclear Information System (INIS)

Van Asch, R.; Verbeek, R.

2009-10-01

In the light of the currently running subsidy programme for particulate filters in the Netherlands, the Dutch ministry of spatial planning and environment (VROM) asked TNO to execute a desk study to evaluate the particulates filtration efficiency of retrofit particulate filters for light duty vehicles (passenger cars and vans). The typical retrofit particulate filters for light duty vehicles are also called 'open' or 'half-open' filters, because a part of the exhaust gas can pass through the particulate filter unfiltered. From design point they are very different from the majority of the factory installed particulate filters, which are also called wall-flow or 'closed' particulate filters. Due to these differences there is a large difference in filtration efficiency. Whereas the 'dosed' particulate filters show a filtration efficiency of larger than 90%, the filtration efficiency of 'open' particulate filters is generally lower (type approval minimum 30%), and strongly dependent on the conditions of use. The objective of the current project was to assess the average filtration efficiency of retrofit (open) particulate fillters on light duty vehicles in real world day to day driving, based on available literature data. Also, the reasons of a possible deviation with the type approval test results (minimum filtration efficiency of 30%) was investigated.

Soil separator and sampler and method of sampling

Science.gov (United States)

O'Brien, Barry H [Idaho Falls, ID; Ritter, Paul D [Idaho Falls, ID

2010-02-16

A soil sampler includes a fluidized bed for receiving a soil sample. The fluidized bed may be in communication with a vacuum for drawing air through the fluidized bed and suspending particulate matter of the soil sample in the air. In a method of sampling, the air may be drawn across a filter, separating the particulate matter. Optionally, a baffle or a cyclone may be included within the fluidized bed for disentrainment, or dedusting, so only the finest particulate matter, including asbestos, will be trapped on the filter. The filter may be removable, and may be tested to determine the content of asbestos and other hazardous particulate matter in the soil sample.

The investigation of atmospheric particulate matter pollution in Suzhou

International Nuclear Information System (INIS)

Chen Yi'ou; Zhang Yuliang; Wang Ya; Wang Pei; Tian Hailin

2012-01-01

Objective: To investigate the pollution status, vertical distribution and concentration variation within 24 hours of total suspended particles (TSPs), particulate matter ≤10 μm (PM10), particulate matter ≤5 (PM5) and particulate matter ≤2.5 μm (PM2.5) in major functional areas of Suzhou and the protective effect of different type masks on particulate matter. Methods: (1) The concentration of atmospheric TSPs, PM10, PM5 and PM2.5 in seven functional areas in Suzhou was monitored for three consecutive days. (2) A residential building of 25 stories was chosen and the concentration of TSPs, PM10, PM5, PM2.5 was detected at the 1st, 5th, 10th, 15th, 20 th and the 25th floor respectively. (3) The concentrations of the four particulate matter were detected every two-hours for three consecutive days to investigate how concentration of particulate matter varies within 24 hours. (4) The concentration of the four kinds of particulate matter was analyzed with the sampling head of monitor wrapped with disposable non-woven medical mask, fashion-type mask, gauze mask or activated carbon anti-dust mask respectively, and the protective effect of the four masks on particulate matter was compared. Results: (1) The concentration of PM2.5 was higher than the national health limit in all seven functional areas in Suzhou. (2) No significant difference in vertical distribution of particulate matter was found among different floors in residential buildings (P>0.05). (3) Two small peaks of particulate matter appeared in the morning and evening respectively while the top appeared at dawn (P< 0.05). (4) Disposable non-woven medical mask showed the best protective effect on particulate matter among the four tested masks. Conclusion: PM2.5 is the main particulate matter in Suzhou area. In addition the 4 kinds of particulate matter: TSP, PM10, PM5 and PM2.5 are of higher concentration in the early morning. No significant difference was detected from an altitude of less than 75 meters

Particulate matter urban air pollution from traffic car

Science.gov (United States)

Filip, G. M.; Brezoczki, V. M.

2017-05-01

The particulate matters (PM) are very important compounds of urban air pollution. There are a lot of air pollution sources who can generate PM and one of the most important of them it is urban traffic car. Air particulate matters have a major influence on human health so everywhere are looking for PM reducing solutions. It is knows that one of the solution for reduce the PM content from car traffic on ambient urban air is the fluidity of urban traffic car by introduction the roundabout intersections. This paper want to present some particulate matter determinations for PM10 and PM2.5 conducted on the two types of urban intersection respectively traffic light and roundabout intersections in Baia Mare town in the approximate the same work conditions. The determinations were carried out using a portable particulate matter monitor Haz - Dust model EPAM - 5000, who can provide a real time data for PM10, PM 2.5.Determinations put out that there are differences between the two locations regarding the PM content on ambient air. On roundabout intersection the PM content is less than traffic light intersection for both PM10 and PM 2.5 with more than 30%.

Concentration and movement of neonicotinoids as particulate matter downwind during agricultural practices using air samplers in southwestern Ontario, Canada.

Science.gov (United States)

Forero, Luis Gabriel; Limay-Rios, Victor; Xue, Yingen; Schaafsma, Arthur

2017-12-01

Atmospheric emissions of neonicotinoid seed treatment insecticides as particulate matter in field crops occur mainly for two reasons: 1) due to abraded dust of treated seed generated during planting using vacuum planters, and 2) as a result of disturbances (tillage or wind events) in the surface of parental soils which release wind erodible soil-bound residues. In the present study, concentration and movement of neonicotinoids as particulate matter were quantified under real conditions using passive and active air samplers. Average neonicotinoid concentrations in Total Suspended Particulate (TSP) using passive samplers were 0.48 ng/cm 2 , trace, trace (LOD 0.80 and 0.04 ng/cm 2 for clothianidin and thiamethoxam, respectively), and using active samplers 16.22, 1.91 and 0.61 ng/m 3 during planting, tillage and wind events, respectively. There was a difference between events on total neonicotinoid concentration collected in particulate matter using either passive or active sampling. Distance of sampling from the source field during planting of treated seed had an effect on total neonicotinoid air concentration. However, during tillage distance did not present an effect on measured concentrations. Using hypothetical scenarios, values of contact exposure for a honey bee were estimated to be in the range from 1.1% to 36.4% of the reference contact LD 50 value of clothianidin of 44 ng/bee. Copyright © 2017 Elsevier Ltd. All rights reserved.

The fate of particulate emissions from an isolated power plant in the oil sands area of western Canada

International Nuclear Information System (INIS)

Barrie, L.A.

1980-01-01

The nature and fate of particulate emissions from an isolated power plant in the Athabasca oil sands area of western Canada are investigated on the basis of measurements of particulate elemental concentrations in the air 80 km from the source late one winter, and close to the source early the next summer, of dry deposition patterns of particulate sulfur and heavy metals in the early summer, and of total (wet and dry) deposition patterns of major ions and metals during two winters. Results of plume chemistry studies to investigate SO 2 oxidation during summer and winter and of fly-ash analyses for heavy metals are also used. It is found that: (1) many elements in particulate matter deposited around the plant originate primarily from a different source in summer and in winter (2) deposition near the source is more alkaline than in outlying areas, (3) wet and dry deposition of acidic oxides of sulfur and nitrogen from the power-plant emissions appear to be the main source of snowpack acidification in downwind areas, and (4) acidic compounds can be transported over long distances before being removed

Baumot BA-B Diesel Particulate Filter with Pre-Catalyst (ETV Mobile Source Emissions Control Devices) Verification Report

Science.gov (United States)

The Baumot BA-B Diesel Particulate Filter with Pre-Catalyst is a diesel engine retrofit device for light, medium, and heavy heavy-duty diesel on-highway engines for use with commercial ultra-low-sulfur diesel (ULSD) fuel. The BA-B particulate filter is composed of a pre-catalyst ...

Characterization and source apportionment of fine particulate sources at Rijeka, Croatia from 2013 to 2015

Energy Technology Data Exchange (ETDEWEB)

Ivošević, Tatjana, E-mail: tatjana.ivosevic14@gmail.com [Faculty of Engineering, University of Rijeka, Vukovarska 58, HR-51000 Rijeka (Croatia); Stelcer, Eduard [Australian Nuclear Science and Technology Organisation, Locked Bag 2001, Kirrawee DC, NSW 2232 (Australia); Orlić, Ivica [Department of Physics, University of Rijeka, Radmile Matejčić 2, HR-51000 Rijeka (Croatia); Bogdanović Radović, Iva [Laboratory for Ion Beam Interactions, Ruđer Bošković Institute, Bijenička 54, HR-10000 Zagreb (Croatia); Cohen, David [Australian Nuclear Science and Technology Organisation, Locked Bag 2001, Kirrawee DC, NSW 2232 (Australia)

2016-03-15

PM{sub 2.5} daily aerosol samples were collected in Rijeka, Croatia during period from 6th August 2013 to 29th January 2015. In total, 259 samples were collected on Teflon filters and analyzed by PIXE and PIGE techniques to give information on 21 elements from Na to Pb. Additionally, black carbon was determined with the Laser Integrated Plate Method. Results were statistically evaluated using Positive Matrix Factorization (PMF). Eight major pollution sources: auto, smoke, secondary sulfates, heavy oil combustion, sea spray, road dust, industry iron and soil dust were identified together with their relative contributions in total PM{sub 2.5} pollution.

40 CFR 92.117 - Gas meter or flow instrumentation calibration, particulate measurement.

Science.gov (United States)

2010-07-01

... 40 Protection of Environment 20 2010-07-01 2010-07-01 false Gas meter or flow instrumentation... ENGINES Test Procedures § 92.117 Gas meter or flow instrumentation calibration, particulate measurement. (a) Sampling for particulate emissions requires the use of gas meters or flow instrumentation to...

Exposure to carbon monoxide, respirable suspended particulates, and volatile organic compounds while commuting by bicycle

International Nuclear Information System (INIS)

Bevan, M.A.J.; Proctor, C.J.; Baker-Rogers, J.; Warren, N.D.

1991-01-01

A portable air sampling system has been used to assess exposures to various substances while commuting by bicycle in an urban area. The major source of pollutants in this situation is motor vehicle exhaust emissions. Carbon monoxide, measured by electrochemical detection, was found at peak concentrations in excess of 62 ppm, with mean values over 16 individual 35-mm journeys being 10.5 ppm. Respirable suspended particulates, averaged over each journey period, were found at higher concentrations (mean 130 μg m -3 ) than would be expected in indoor situations. Mean exposure to benzene (at 56 μg m -3 ) and other aromatic volatile organic compounds was also relatively high. The influence of wind conditions on exposure was found to be significant. Commuting exposures to carbon monoxide, respirable suspended particulates, and aromatic VOCs were found to be higher than exposures in a busy high street and on common parkland

Open source laboratory sample rotator mixer and shaker

Directory of Open Access Journals (Sweden)

Karankumar C. Dhankani

2017-04-01

Full Text Available An open-source 3-D printable laboratory sample rotator mixer is developed here in two variants that allow users to opt for the level of functionality, cost saving and associated complexity needed in their laboratories. First, a laboratory sample rotator is designed and demonstrated that can be used for tumbling as well as gentle mixing of samples in a variety of tube sizes by mixing them horizontally, vertically, or any position in between. Changing the mixing angle is fast and convenient and requires no tools. This device is battery powered and can be easily transported to operate in various locations in a lab including desktops, benches, clean hoods, chemical hoods, cold rooms, glove boxes, incubators or biological hoods. Second, an on-board Arduino-based microcontroller is incorporated that adds the functionality of a laboratory sample shaker. These devices can be customized both mechanically and functionally as the user can simply select the operation mode on the switch or alter the code to perform custom experiments. The open source laboratory sample rotator mixer can be built by non-specialists for under US$30 and adding shaking functionality can be done for under $20 more. Thus, these open source devices are technically superior to the proprietary commercial equipment available on the market while saving over 90% of the costs.

Determination of particulate lead using aerosol mass spectrometry: MILAGRO/MCMA-2006 observations

Directory of Open Access Journals (Sweden)

D. Salcedo

2010-06-01

Full Text Available We report the first measurements of particulate lead (Pb from Aerodyne Aerosol Mass Spectrometers, which were deployed in and around Mexico City during the Megacity Initiative: Local and Global Research Observations (MILAGRO/Mexico City Metropolitan Area 2006 (MCMA-2006 field campaigns. The high resolution mass spectrometer of one of the AMS instruments (HR-AMS and the measured isotopic ratios unequivocally prove the detection of Pb in ambient particles. A substantial fraction of the lead evaporated slowly from the vaporizer of the instruments, which is indicative of species with low volatility at 600 °C. A model was developed in order to estimate the ambient particulate Pb entering the AMS from the signals in the "open" and the "closed" (or "background" mass spectrum modes of the AMS. The model suggests the presence of at least two lead fractions with ~25% of the Pb signal exhibiting rapid evaporation (1/e decay constant, τ<0.1 s and ~75% exhibiting slow evaporation (τ~2.4 min at the T0 urban supersite and a different fraction (70% prompt and 30% slow evaporation at a site northwest from the metropolitan area (PEMEX site. From laboratory experiments with pure Pb(NO₃₂ particles, we estimated that the Pb ionization efficiency relative to nitrate (RIE_Pb is 0.5. Comparison of time series of AMS Pb with other measurements carried out at the T0 supersite during MILAGRO (using Proton Induced X-ray Emission (PIXE, Inductively-Coupled Plasma Mass Spectrometry (ICP-MS and single-particle counts from an Aerosol Time-of-Fight Mass Spectrometer (ATOFMS shows similar levels (for PIXE and ICP-MS and substantial correlation. During part of the campaign, sampling at T0 was alternated every 10 min with an Aerosol Concentrator, which enabled the detection of signals for PbCl⁺ and PbS⁺ ions. PbS⁺ displays the signature of a slowly evaporating species, while PbCl⁺ appears to arise only

Monte Carlo stratified source-sampling

International Nuclear Information System (INIS)

Blomquist, R.N.; Gelbard, E.M.

1997-01-01

In 1995, at a conference on criticality safety, a special session was devoted to the Monte Carlo open-quotes eigenvalue of the worldclose quotes problem. Argonne presented a paper, at that session, in which the anomalies originally observed in that problem were reproduced in a much simplified model-problem configuration, and removed by a version of stratified source-sampling. The original test-problem was treated by a special code designed specifically for that purpose. Recently ANL started work on a method for dealing with more realistic eigenvalue of the world configurations, and has been incorporating this method into VIM. The original method has been modified to take into account real-world statistical noise sources not included in the model problem. This paper constitutes a status report on work still in progress

[Sampling methods for PM2.5 from stationary sources: a review].

Science.gov (United States)

Jiang, Jing-Kun; Deng, Jian-Guo; Li, Zhen; Li, Xing-Hua; Duan, Lei; Hao, Ji-Ming

2014-05-01

The new China national ambient air quality standard has been published in 2012 and will be implemented in 2016. To meet the requirements in this new standard, monitoring and controlling PM2,,5 emission from stationary sources are very important. However, so far there is no national standard method on sampling PM2.5 from stationary sources. Different sampling methods for PM2.5 from stationary sources and relevant international standards were reviewed in this study. It includes the methods for PM2.5 sampling in flue gas and the methods for PM2.5 sampling after dilution. Both advantages and disadvantages of these sampling methods were discussed. For environmental management, the method for PM2.5 sampling in flue gas such as impactor and virtual impactor was suggested as a standard to determine filterable PM2.5. To evaluate environmental and health effects of PM2.5 from stationary sources, standard dilution method for sampling of total PM2.5 should be established.

Level, potential sources of polycyclic aromatic hydrocarbons (PAHs) in particulate matter (PM10) in Naples

Science.gov (United States)

Di Vaio, Paola; Cocozziello, Beatrice; Corvino, Angela; Fiorino, Ferdinando; Frecentese, Francesco; Magli, Elisa; Onorati, Giuseppe; Saccone, Irene; Santagada, Vincenzo; Settimo, Gaetano; Severino, Beatrice; Perissutti, Elisa

2016-03-01

In Naples, particulate matter PM10 associated with polycyclic aromatic hydrocarbons (PAHs) in ambient air were determined in urban background (NA01) and urban traffic (NA02) sites. The principal objective of the study was to determine the concentration and distribution of PAHs in PM10 for identification of their possible sources (through diagnostic ratio - DR and principal component analysis - PCA) and an estimation of the human health risk (from exposure to airborne TEQ). Airborne PM10 samples were collected on quartz filters using a Low Volume Sampler (LVS) for 24 h with seasonal samples (autumn, winter, spring and summer) of about 15 days each between October 2012 and July 2013. The PM10 mass was gravimetrically determined. The PM10 levels, in all seasons, were significantly higher (P gas chromatography-mass spectrometer (GC-MS) analysis. The concentration of Benzo[a]Pyrene, BaP (EU and National limit value: 1 ng m-3 in PM10), varied from 0.065 ng m-3 during autumn time to 0.872 ng m-3 in spring time (NA01) and from 0.120 ng m-3 during autumn time to 1.48 ng m-3 of winter time (NA02) with four overshoots. In NA02 the trend of Σ12 PAHs was comparable to NA01 but were observed higher values than NA01. In fact, the mean concentration of Σ12 PAHs, in urban-traffic site was generally 2 times greater than in urban-background site in all the campaigns. PAHs with 5 and 6 ring, many of which are suspected carcinogens or genotoxic agents, (i.e Benzo[a]Pyrene, Indeno[1,2,3-cd]Pyrene, Benzo[b]Fluoranthene, Benzo[k]Fluoranthene and Benzo[g,h,i]Perylene), had a large contribution (∼50-55%) of total PAHs concentration in PM10 in two sites and in each of the campaigns. Diagnostic ratio analysis and PCA suggested a substantial contributions from traffic emission with minimal influence from coal combustion and natural gas emissions. In particular diesel vehicular emissions were the major source of PAHs at the studied sites. The use of Toxicity Equivalence Quantity (TEQ

Distribution of lead-210 and polonium-210 between soluble and particulate phases in seawater

International Nuclear Information System (INIS)

Spencer, D.W.

1975-01-01

Results are reported from radiometric measurements of the distribution of 210 Pb and 210 Po in surface seawater and suspended particulate matter. Samples of plankton and sediments collected from some locations were also analyzed. Samples of seawater and suspended particulate matter were collected from stations located in the Gulf of Maine, the North Atlantic, and approximately 500 miles southwest of Gilbraltar. (U.S.)

Long-term measurements of respirable sulfates and particulates inside and outside homes

Energy Technology Data Exchange (ETDEWEB)

Spengler, J D; Dockery, D W; Turner, W A; Wolfson, J M; Ferris, B G

1981-01-01

To better understand the health effects of air pollution, the results of extensive indoor and outdoor measurements of mass respirable particulates and water-soluble respirable particulates are analyzed. The measurements were taken in six U.S. citiesPortage, Wis./ Topeka, Kans./ Kingston/Harriman, Tenn./ Watertown, Mass./ St. Louis, Mo./ and Steubenville, Ohio. Results indicated that the major source of indoor air pollution is cigarette smoke, which contributes about 20

High-Latitude Wintertime Urban Pollution: Particulate Matter Composition and Temporal Trends in Fairbanks, Alaska

Science.gov (United States)

Simpson, W. R.; Nattinger, K.; Hooper, M.

2017-12-01

High latitude cities often experience severe pollution episodes during wintertime exacerbated by thermal inversion trapping of pollutant emissions. Fairbanks, Alaska is an extreme example of this problem, currently being classified by the US Environmental Protection Agency (EPA) as a "serious" non-attainment area for fine particulate matter (PM2.5). For this reason, we have studied the chemical composition of PM2.5 at multiple EPA monitoring sites in the non-attainment area from 2006 to the present. The chemical composition is dominated by organic carbon with lesser amounts of black carbon and inorganic ionic species such as ammonium, sulfate, and nitrate. We find large spatial differences in composition and amount of PM2.5 that indicate a different mix of sources in residential areas as compared to the city center. Specifically, the difference in composition is consistent with increased wood smoke source in the residential areas. The extent to which organic matter could be secondary (formed through conversion of emitted gases) is also an area needing study. Ammonium sulfate is responsible for about a fifth to a quarter of the particles mass during the darkest months, possibly indicating a non-photochemical source of sulfate, but the chemical mechanism for this possible transformation is unclear. Therefore, we quantified the relationship between particulate sulfate concentrations and gas-phase sulfur dioxide concentrations along with particulate metals and inferred particulate acidity with the hopes that these data can assist in elucidation of the mechanism of particulate sulfate formation. We also analyze temporal trends in PM2.5 composition in an attempt to understand how the problem is changing over time and find most trends are small despite regulatory changes. Improving mechanistic understanding of particulate formation under cold and dark conditions could assist in reducing air-quality-related health effects.

Saccharide Composition in Fine and Coarse Particulate Matter and Soils in Central Arizona and Use of Saccharides as Molecular Markers for Source Apportionment

Science.gov (United States)

Jia, Y.; Clements, A.; Fraser, M.

2009-04-01

The desert southwestern United States routinely exceeds health-based standards for coarse particulate matter [1]. PM10 concentrations are high in both urban and rural areas and are believed to originate from fugitive dust emissions from agricultural fields and roads and soil erosion from the surrounding desert locations. Soil together with its associated biota contains a complex mixture of biogenic detritus, including plant detritus, airborne microbes comprised of bacteria, viruses, spores of lichens and fungi, small algae, and protozoan cysts [4][5], which can mostly become airborne when winds are strong enough and soil dry enough to be re-entrained into the atmosphere [3]. Other potential sources to PM10 may include primary biological aerosol particles (PBAPs), given a multitude of flower, grass, and fungal species that thrive in the Sonoran desert and actively release pollens and spores throughout the year [2]. However, because soil and fugitive dust is also believed to contain a large number of these biological particles and is considered as a secondary host of PBAPs [3] [4], the role and contribution of PBAPs as a direct ambient PM source in the desert southwest have not been clearly stated or investigated. In an effort to identify and assess the relative contribution of these and other major PM sources in the southwestern US region, and particularly to assess the contribution from soil and fugitive dust, a series of ambient PM samples and soil samples were collected in Higley, AZ, USA, a suburb of the Phoenix metropolitan area which has seen rapid urban sprawl onto agricultural lands. Because of their suggested ability to track biologically important organic materials from natural environment [4][6][7][8][9][10], saccharides were chosen as the key compounds to trace the release of soil dusts into the atmosphere, and to elucidate other major sources that contribute to the PM levels in this location in the arid southwestern US. To this end, saccharide compounds

Aerosol composition and source apportionment in the Mexico City Metropolitan Area with PIXE/PESA/STIM and multivariate analysis

OpenAIRE

Johnson , K. S.; De Foy , B.; Zuberi , B.; Molina , L. T.; Molina , M. J.; Xie , Y.; Laskin , A.; Shutthanandan , V.

2006-01-01

Aerosols play an important role in the atmosphere but are poorly characterized, particularly in urban areas like the Mexico City Metropolitan Area (MCMA). The chemical composition of urban particles must be known to assess their effects on the environment, and specific particulate emissions sources should be identified to establish effective pollution control standards. For these reasons, samples of particulate matter ≤2.5 μm (PM_2.5) were collected dur...

INAA in combination with other analytical techniques in the study of urban aerosol sources

International Nuclear Information System (INIS)

Binh, N.T.; Truong, Y.; Ngo, N.T.; Sieu, L.N.; Hien, P.D.

2000-01-01

Concentrations of elements in fine and coarse PM10 samples collected in Ho Chi Minh City were determined by INAA for the purpose of characterising air pollution sources using multivariate receptor modeling techniques. Seven sources common to coarse and fine samples were identified. Resuspended soil dust is dominant in the coarse samples accounting for 41% of the particulate mass. In the fine samples, vehicle emissions and coal burning are most important accounting for about 20% each. Although a great number of elements were included in the input data for receptor modeling, the interpretation of emission sources was not always straightforward. Information on other source markers were needed. Therefore, a polarography method was used for quantifying lead, and recently, ion chromatography method became available for quantifying secondary sulphates, nitrates and other water soluble ions. (author)

Key sources and distribution patterns of particulate material in the South Atlantic: data from the UK GEOTRACES A10 cruise

Science.gov (United States)

Milne, A.; Palmer, M.; Lohan, M. C.

2016-02-01

Particles play a fundamental role in the biogeochemical cycling of both major- and micro-nutrients in marine systems, including trace elements and isotopes. However, knowledge of particulate distributions, and their potential to regulate dissolved elemental concentrations, remains limited and poorly understood. The paradox is, that the oceanic inventory of trace metals is dominated by particulate inputs (e.g. aerosol deposition, shelf sediment resuspension). Moreover the labile fraction of particulate trace elements could be an important regulator of dissolved concentrations. Here we present particulate data from the UK GEOTRACES South Atlantic transect (GA10) from South Africa to Uruguay. Data from a range of elements (e.g. Fe, Al, Mn) revealed a greater input of particulate metals from the Argentine shelf (up to 290 nM of pFe) in comparison to the South African shelf (basin and penetrated deeper up the water column (up to 1300 m), a result of intense benthic storms. The imprint of leakage from the Agulhas Current, identified through temperature and salinity, was observed in the upper water column profile of numerous particulate data (e.g. Pb, Ni, Cd). Measured elemental gradients, combined with measurements from a vertical mixing-profiler, will allow estimates of particulate fluxes to be calculated.

Characterization of size, number, concentration and morphology of particulate matter emitted from a high performance diesel combustion system using biomass derived fuels

Energy Technology Data Exchange (ETDEWEB)

Bhardwaj, Om Parkash; Krishnamurthy, Ketan; Kremer, Florian; Pischinger, Stefan [RWTH Aachen Univ. (Germany). Inst. for Combustion Engines; Berg, Angelika von; Roth, Georg [RWTH Aachen Univ. (Germany). Inst. of Crystallography; Lueers, Bernhard; Kolbeck, Andreas; Koerfer, Thomas [FEV GmbH, Aachen (Germany)

2013-06-01

Motor vehicle emissions have been identified as a major source of particulates. Although the low limits of particulate matter cause a need for a particulate trap in most of the present day diesel engines, the physical and chemical characterization of particles with the measures of size, number, volatility and reactivity etc. is of increasing interest with respect to the regeneration frequency and regeneration efficiency of a particulate trap. Within the Cluster of Excellence ''Tailor-Made Fuels from Biomass (TMFB)'' at RWTH Aachen University, the Institute for Combustion Engines carried out a detailed investigation program to explore the potential of future biofuel candidates for future combustion systems. The experiments for particulate measurements and analysis were conducted on a EURO 6 compliant High Efficiency Diesel Combustion System (HECS) with petroleum based diesel fuel as reference and today's biofuel (i.e. FAME) as well as a potential future biomass derived fuel candidate (i.e. 2-MTHF I DBE), being developed under TMFB approach. Soot samples collected on polycarbonate filters were analyzed using SEM; revealing vital informations regarding particle size distribution. Furthermore, thermophoretic sampling was also performed on copper grids and samples were analyzed using TEM to determine its graphitic micro-structure. In addition, X-Ray diffraction (XRD) measurements were also performed to get further quantitative information regarding crystal lattice parameters and structure of investigated soot. The results indicate more than 90% reduction in the mass and number concentrations of engine out particle emissions using future biomass derived fuel candidate. A good co-relation was observed between TEM micro-structure results and quantitative crystal lattice and structure information obtained from XRD studies, indicating higher reactivity for soot emitted from 2-MTHF/DBE. (orig.)

PM10 standards and nontraditional particulate source controls: Research perspective

International Nuclear Information System (INIS)

Watson, J.G.

1992-01-01

Knowledge of how to measure suspended particles, what their concentrations are, what they are composed of, and where they come from has increased substantially since 1975. At that time, much of the pioneering work in these areas was just being conducted and published. Size-classified measurements, low-level elemental analysis, inorganic ion analysis, and carbon determinations for aerosol samples were novel research developments. Receptor modeling was not considered to be a scientific discipline, let alone a useful tool for source apportionment. Presentations at earlier conferences went to great lengths to document and justify methodologies which are taken for granted at this conference. This paper goes on to discuss research findings in control of wood smoke, fugitive dusts, motor vehicle exhausts, and secondary aerosols. Research results in source apportionment are also discussed

The Bologna complete sample of nearby radio sources. II. Phase referenced observations of faint nuclear sources

Science.gov (United States)

Liuzzo, E.; Giovannini, G.; Giroletti, M.; Taylor, G. B.

2009-10-01

Aims: To study statistical properties of different classes of sources, it is necessary to observe a sample that is free of selection effects. To do this, we initiated a project to observe a complete sample of radio galaxies selected from the B2 Catalogue of Radio Sources and the Third Cambridge Revised Catalogue (3CR), with no selection constraint on the nuclear properties. We named this sample “the Bologna Complete Sample” (BCS). Methods: We present new VLBI observations at 5 and 1.6 GHz for 33 sources drawn from a sample not biased toward orientation. By combining these data with those in the literature, information on the parsec-scale morphology is available for a total of 76 of 94 radio sources with a range in radio power and kiloparsec-scale morphologies. Results: The fraction of two-sided sources at milliarcsecond resolution is high (30%), compared to the fraction found in VLBI surveys selected at centimeter wavelengths, as expected from the predictions of unified models. The parsec-scale jets are generally found to be straight and to line up with the kiloparsec-scale jets. A few peculiar sources are discussed in detail. Tables 1-4 are only available in electronic form at http://www.aanda.org

Activation analysis of air particulate matter

International Nuclear Information System (INIS)

Alian, A.; Sansoni, B.

1988-11-01

This review on activation analysis of air particulate matter is an extended and updated version of a review given by the same authors in 1985. The main part is aimed at the analytical scheme and refers to rules and techniques for sampling, sample and standard preparation, irradiation and counting procedures, as well as data processing, - evaluation, and - presentation. Additional chapters deal with relative and monostandard methods, the use of activation analysis for atmosphere samples in various localities, and level of toxic and other elements in the atmosphere. The review contains 190 references. (RB)

Preliminary PM2.5 and PM10 fractions source apportionment complemented by statistical accuracy determination

Directory of Open Access Journals (Sweden)

Samek Lucyna

2016-03-01

Full Text Available Samples of PM10 and PM2.5 fractions were collected between the years 2010 and 2013 at the urban area of Krakow, Poland. Numerous types of air pollution sources are present at the site; these include steel and cement industries, traffic, municipal emission sources and biomass burning. Energy dispersive X-ray fluorescence was used to determine the concentrations of the following elements: Cl, K, Ca, Ti, Mn, Fe, Ni, Cu, Zn, Br, Rb, Sr, As and Pb within the collected samples. Defining the elements as indicators, airborne particulate matter (APM source profiles were prepared by applying principal component analysis (PCA, factor analysis (FA and multiple linear regression (MLR. Four different factors identifying possible air pollution sources for both PM10 and PM2.5 fractions were attributed to municipal emissions, biomass burning, steel industry, traffic, cement and metal industry, Zn and Pb industry and secondary aerosols. The uncertainty associated with each loading was determined by a statistical simulation method that took into account the individual elemental concentrations and their corresponding uncertainties. It will be possible to identify two or more sources of air particulate matter pollution for a single factor in case it is extremely difficult to separate the sources.

Impact of maritime traffic on polycyclic aromatic hydrocarbons, metals and particulate matter in Venice air.

Science.gov (United States)

Gregoris, Elena; Barbaro, Elena; Morabito, Elisa; Toscano, Giuseppa; Donateo, Antonio; Cesari, Daniela; Contini, Daniele; Gambaro, Andrea

2016-04-01

Harbours are important hubs for economic growth in both tourism and commercial activities. They are also an environmental burden being a source of atmospheric pollution often localized near cities and industrial complexes. The aim of this study is to quantify the relative contribution of maritime traffic and harbour activities to atmospheric pollutant concentration in the Venice lagoon. The impact of ship traffic was quantified on various pollutants that are not directly included in the current European legislation for shipping emission reduction: (i) gaseous and particulate PAHs; (ii) metals in PM10; and (iii) PM10 and PM2.5. All contributions were correlated with the tonnage of ships during the sampling periods and results were used to evaluate the impact of the European Directive 2005/33/EC on air quality in Venice comparing measurements taken before and after the application of the Directive (year 2010). The outcomes suggest that legislation on ship traffic, which focused on the issue of the emissions of sulphur oxides, could be an efficient method also to reduce the impact of shipping on primary particulate matter concentration; on the other hand, we did not observe a significant reduction in the contribution of ship traffic and harbour activities to particulate PAHs and metals. Graphical abstract Impact of maritime traffic on polycyclic aromatic hydrocarbons, metals and particulate matter and evaluation of the effect of an European Directive on air quality in Venice.

Occurrence, characterisation and fate of (nano)particulate Ti and Ag in two Norwegian wastewater treatment plants

DEFF Research Database (Denmark)

Polesel, Fabio; Farkas, Julia; Kjos, Marianne

2018-01-01

was conducted in two full-scale WWTPs in Trondheim (Norway) employing only primary treatment. We assessed the occurrence and elimination of Ti and Ag, and conducted size-based fractionation using sequential filtration of influent samples to separate particulate, colloidal and dissolved fractions. Eight...... concentration patterns (especially total suspended solids), with peaks during the morning and/or evening and minima at night, indicating household discharges as predominant source. Irregular profiles were exhibited by influent Ag, with periodic concentration spikes suggesting short-term discharges from one...

Battery condenser system particulate emission factors for cotton gins: Particle size distribution characteristics

Science.gov (United States)

This report is part of a project to characterize cotton gin emissions from the standpoint of total particulate stack sampling and particle size analyses. In 2013, the Environmental Protection Agency (EPA) published a more stringent standard for particulate matter with nominal diameter less than or e...

Source apportionment of traffic emissions of particulate matter using tunnel measurements

Science.gov (United States)

Lawrence, Samantha; Sokhi, Ranjeet; Ravindra, Khaiwal; Mao, Hongjun; Prain, Hunter Douglas; Bull, Ian D.

2013-10-01

This study aims to quantify exhaust/non-exhaust emissions and the uncertainties associated with them by combining innovative motorway tunnel sampling and source apportionment modelling. Analytical techniques ICP-AES and GC-MS were used to identify the metallic and organic composition of PM10, respectively. Good correlation was observed between Fe, Cu, Mn, Ni, Pb and Sb and change in traffic volume. The concentration of polycyclic aromatic hydrocarbons and other organics varies significantly at the entrance and exit site of the tunnel, with fluoranthene, pyrene, benzo[a]pyrene, chrysene and benzothiazole having the highest incremented concentrations. The application of Principal Component Analysis and Multiple Linear Regression Analysis helped to identify the emission sources for 82% of the total PM10 mass inside the tunnel. Identified sources include resuspension (27%), diesel exhaust emissions (21%), petrol exhaust emissions (12%), brake wear emissions (11%) and road surface wear (11%). This study shows that major health related chemical species of PM10 originate from non-exhaust sources, further signifying the need for legislation to reduce these emissions.

Atmospheric trace metal concentrations in Suspended Particulate ...

African Journals Online (AJOL)

The air particulate samples were collected from the kitchens, living rooms and outdoor environment of five households in the community. The quantification of the trace metals was done using Atomic Absorption spectrometry method, employing HNO based wet digestion. High baseline concentration of SPMwere obtained ...

A critical review of nuclear activation techniques for the determination of trace elements in atmospheric aerosols, particulates and sludge samples

International Nuclear Information System (INIS)

Dams, R.

1992-01-01

Activation analysis is one of the major techniques for the determination of many minor and trace elements in a large variety of solid environmental and pollution samples, such as atmospheric aerosols, particulate emissions, fly ash, coal, incineration ash and sewage sludge, etc. Neutron activation analysis of total, inhalable or respirable airborne particulate matter collected on a filter or in a cascade impactor on some substrate, is very popular. By Instrumental Neutron Activation Analysis (INAA) up to 45 elements can be determined. The irradiation and counting procedures can be adapted to optimize the sensitivity for particular elements. The precision is largely governed by counting statistics and a high accuracy can be obtained after calibration with multi-elemental standards. Radiochemical Neutron Activation Analysis (RNAA) is applied only when extremely low limits of determination are required. Instrumental Photon Activation Analysis (IPAA) is complementary to INAA, since some elements of environmental interest can be determined which do not produce appropriate radionuclides by neutron irradiation. Charged Particle Activation Analysis (CPAA) is used in particular circumstances such as for certification purposes or coupled to radiochemical separations for extremely low concentrations. (author)

Remote monitoring of environmental particulate pollution - A problem in inversion of first-kind integral equations

Science.gov (United States)

Fymat, A. L.

1975-01-01

The determination of the microstructure, chemical nature, and dynamical evolution of scattering particulates in the atmosphere is considered. A description is given of indirect sampling techniques which can circumvent most of the difficulties associated with direct sampling techniques, taking into account methods based on scattering, extinction, and diffraction of an incident light beam. Approaches for reconstructing the particulate size distribution from the direct and the scattered radiation are discussed. A new method is proposed for determining the chemical composition of the particulates and attention is given to the relevance of methods of solution involving first kind Fredholm integral equations.

Evaluating the suitability of different environmental samples for tracing atmospheric pollution in industrial areas.

Science.gov (United States)

Francová, Anna; Chrastný, Vladislav; Šillerová, Hana; Vítková, Martina; Kocourková, Jana; Komárek, Michael

2017-01-01

Samples of lichens, snow and particulate matter (PM 10 , 24 h) are used for the source identification of air pollution in the heavily industrialized region of Ostrava, Upper Silesia, Czech Republic. An integrated approach that uses different environmental samples for metal concentration and Pb isotope analyses was applied. The broad range of isotope ratios in the samples indicates a combination of different pollution sources, the strongest among them being the metallurgical industry, bituminous coal combustion and traffic. Snow samples are proven as the most relevant indicator for tracing metal(loid)s and recent local contamination in the atmosphere. Lichens can be successfully used as tracers of the long-term activity of local and remote sources of contamination. The combination of PM 10 with snow can provide very useful information for evaluation of current pollution sources. Copyright © 2016 Elsevier Ltd. All rights reserved.

New complete sample of identified radio sources. Part 2. Statistical study

International Nuclear Information System (INIS)

Soltan, A.

1978-01-01

Complete sample of radio sources with known redshifts selected in Paper I is studied. Source counts in the sample and the luminosity - volume test show that both quasars and galaxies are subject to the evolution. Luminosity functions for different ranges of redshifts are obtained. Due to many uncertainties only simplified models of the evolution are tested. Exponential decline of the liminosity with time of all the bright sources is in a good agreement both with the luminosity- volume test and N(S) realtion in the entire range of observed flux densities. It is shown that sources in the sample are randomly distributed in scales greater than about 17 Mpc. (author)

Aerosol composition and source apportionment in the Mexico City Metropolitan Area with PIXE/PESA/STIM and multivariate analysis

OpenAIRE

K. S. Johnson; B. de Foy; B. de Foy; B. Zuberi; B. Zuberi; L. T. Molina; L. T. Molina; M. J. Molina; M. J. Molina; Y. Xie; A. Laskin; V. Shutthanandan

2006-01-01

Aerosols play an important role in the atmosphere but are poorly characterized, particularly in urban areas like the Mexico City Metropolitan Area (MCMA). The chemical composition of urban particles must be known to assess their effects on the environment, and specific particulate emissions sources should be identified to establish effective pollution control standards. For these reasons, samples of particulate matter ≤2.5 μm (PM2.5) were collected during the MCMA-2003 Field Campaign f...

Barrow Black Carbon Source and Impact Study Final Campaign Report

Energy Technology Data Exchange (ETDEWEB)

Barrett, Tate [Baylor Univ., Waco, TX (United States)

2014-07-01

The goal of the Barrow Black Carbon Source and Impact (BBCSI) Study was to characterize the concentration and isotopic composition of carbonaceous atmospheric particulate matter (PM) at the Atmospheric Radiation Measurement site in Barrow, AK. The carbonaceous component was characterized via measurement of the organic and black carbon (OC and BC) components of the total PM. To facilitate complete characterization of the particulate matter, filter-based collections were used, including a medium volume PM2.5 sampler and a high volume PM10 sampler. Thirty-eight fine (PM2.5) and 49 coarse (PM10) particulate matter fractions were collected at weekly and bi-monthly intervals. The PM2.5 sampler operated with minimal maintenance during the 12 month campaign. The PM10 sampler used for the BBCSI used standard Tisch hi-vol motors which have a known lifetime of ~1 month under constant use; this necessitated monthly maintenance and it is suggested that the motors be upgraded to industrial blowers for future deployment in the Arctic. The BBCSI sampling campaign successfully collected and archived 87 ambient atmospheric particulate matter samples from Barrow, AK from July 2012 to June 2013. Preliminary analysis of the organic and black carbon concentrations has been completed. This campaign confirmed known trends of high BC lasting from the winter through to spring haze periods and low BC concentrations in the summer.

Radiation dose estimates due to air particulate emissions from selected phosphate industry operations

International Nuclear Information System (INIS)

Partridge, J.E.; Horton, T.R.; Sensintaffar, E.L.; Boysen, G.A.

1978-06-01

The EPA Office of Radiation Programs has conducted a series of studies to determine the radiological impact of the phosphate mining and milling industry. This report describes the efforts to estimate the radiation doses due to airborne emissions of particulates from selected phosphate milling operations in Florida. Two wet process phosphoric acid plants and one ore drying facility were selected for this study. The 1976 Annual Operations/Emissions Report, submitted by each facility to the Florida Department of Environmental Regulation, and a field survey trip by EPA personnel to each facility were used to develop data for dose calculations. The field survey trip included sampling for stack emissions and ambient air samples collected in the general vicinity of each plant. Population and individual radiation dose estimates are made based on these sources of data

Determination of trace amounts of rare earth elements in various environmental samples by spark source mass spectrography

International Nuclear Information System (INIS)

Sugimae, Akiyoshi

1978-01-01

A chemical concentration-mass spectrographic procedure was described for the determination of trace amounts of rare earth elements in various environmental samples: airborne particulate matter, dustfall, soil and so forth. A 0.5 to 1 gram of sample material was decomposed by fusion with sodium carbonate. The silica dehydrated in the usual way was filtered off and the filtrate from the silica was then treated with ammonium hydroxide to precipitate the rare earth elements. After ignition of the precipitate, two ml of internal standard solution containing 20 μg/ml of silver were added and the mixture was then evaporated to dryness. The residue was mixed with an equal amount of graphite powder and then pressed into electrodes. Relative sensitivity coefficients (Ag=1.0) were determined by using Spex Mix and U. S. Geological Survey rock standard G-2. U. S. Geological Survey rock standard GSP-1 and N.B.S. coal fly ash SRM 1633 were analysed to evaluate the accuracy of the proposed method. Comparison of the mass spectral values with literature ones indicated a good agreement. The coefficient of variation obtained by replicate analysis of SRM 1633 was better than 25%. The proposed method was applied to the determination of rare earth elements in airborne particulate matter and dustfall collected on polystyrene filter and in dustjars, respectively. Results for the rare earth elements in the blank of glass fiber filter which was widely used for the collection of airborne particulate matter were also presented. (auth.)

Quantification of trace elements and speciation of iron in atmospheric particulate matter

Science.gov (United States)

Upadhyay, Nabin

Trace metal species play important roles in atmospheric redox processes and in the generation of oxidants in cloud systems. The chemical impact of these elements on atmospheric and cloud chemistry is dependent on their occurrence, solubility and speciation. First, analytical protocols have been developed to determine trace elements in particulate matter samples collected for carbonaceous analysis. The validated novel protocols were applied to the determination of trace elements in particulate samples collected in the remote marine atmosphere and urban areas in Arizona to study air pollution issues. The second part of this work investigates on solubility and speciation in environmental samples. A detailed study on the impact of the nature and strength of buffer solutions on solubility and speciation of iron lead to a robust protocol, allowing for comparative measurements in matrices representative of cloud water conditions. Application of this protocol to samples from different environments showed low iron solubility (less than 1%) in dust-impacted events and higher solubility (5%) in anthropogenically impacted urban samples. In most cases, Fe(II) was the dominant oxidation state in the soluble fraction of iron. The analytical protocol was then applied to investigate iron processing by fogs. Field observations showed that only a small fraction (1%) of iron was scavenged by fog droplets for which each of the soluble and insoluble fraction were similar. A coarse time resolution limited detailed insights into redox cycling within fog system. Overall results suggested that the major iron species in the droplets was Fe(1I) (80% of soluble iron). Finally, the occurrence and sources of emerging organic pollutants in the urban atmosphere were investigated. Synthetic musk species are ubiquitous in the urban environment (less than 5 ng m-3) and investigations at wastewater treatment plants showed that wastewater aeration basins emit a substantial amount of these species to

Gaseous and particulate air pollutants in the Northeastern Mediterranean Coast

International Nuclear Information System (INIS)

Soner Erduran, M.; Tuncel, Semra G.

2001-01-01

The concentrations of sulfur dioxide (SO 2 ), ammonia (NH 3 ) and particulate matter were measured for a 6-month period and the concentration of gas phase nitric acid (HNO 3 ) was measured for a 1-month period in the North-eastern Mediterranean atmosphere (Kuecuek Calticak, Antalya) using a 'filter pack' system that was developed and optimised in our laboratory. Among all the gas phase pollutants, HNO 3 had the lowest concentration (0.42 μg m -3 ) followed by ammonia. Most of the measured parameters showed variation in time depending on strengths of source regions and meteorological conditions. Nitric acid is found mostly in particulate form, but gas to particulate partitioning of SO 2 shows seasonal variation. Wind trajectory analyses indicate that the major contribution to the observed concentrations come mostly from Eastern Europe and Blacksea regions as well as the southern sector

Speciation of copper and zinc in size-fractionated atmospheric particulate matter using total reflection mode X-ray absorption near-edge structure spectrometry

International Nuclear Information System (INIS)

Osan, Janos; Meirer, Florian; Groma, Veronika; Toeroek, Szabina; Ingerle, Dieter; Streli, Christina; Pepponi, Giancarlo

2010-01-01

The health effects of aerosol depend on the size distribution and the chemical composition of the particles. Heavy metals of anthropogenic origin are bound to the fine aerosol fraction (PM 2.5 ). The composition and speciation of aerosol particles can be variable in time, due to the time-dependence of anthropogenic sources as well as meteorological conditions. Synchrotron-radiation total reflection X-ray fluorescence (SR-TXRF) provides very high sensitivity for characterization of atmospheric particulate matter. X-ray absorption near-edge structure (XANES) spectrometry in conjunction with TXRF detection can deliver speciation information on heavy metals in aerosol particles collected directly on the reflector surface. The suitability of TXRF-XANES for copper and zinc speciation in size-fractionated atmospheric particulate matter from a short sampling period is presented. For high size resolution analysis, atmospheric aerosol particles were collected at different urban and rural locations using a 7-stage May cascade impactor having adapted for sampling on Si wafers. The thin stripe geometry formed by the particulate matter deposited on the May-impactor plates is ideally suited to SR-TXRF. Capabilities of the combination of the May-impactor sampling and TXRF-XANES measurements at HASYLAB Beamline L to Cu and Zn speciation in size-fractionated atmospheric particulate matter are demonstrated. Information on Cu and Zn speciation could be performed for elemental concentrations as low as 140 pg/m 3 . The Cu and Zn speciation in the different size fraction was found to be very distinctive for samples of different origin. Zn and Cu chemical state typical for soils was detected only in the largest particles studied (2-4 μm fraction). The fine particles, however, contained the metals of interest in the sulfate and nitrate forms.

Source contributions to United States ozone and particulate matter over five decades from 1970 to 2020

Science.gov (United States)

Nopmongcol, Uarporn; Alvarez, Yesica; Jung, Jaegun; Grant, John; Kumar, Naresh; Yarwood, Greg

2017-10-01

Evaluating long-term air quality trends can demonstrate effectiveness of control strategies and guide future air quality management planning. Observations have shown that ozone (O3) and fine particulate matter (PM2.5) in the US have declined since as early as 1980 in some areas. But observation trends alone cannot separate effects of changes in local and global emissions to US air quality which are important to air quality planners. This study uses a regional model (CAMx) nested within a global model (GEOS-Chem) to characterize regional changes in O3 and PM2.5 due to the intercontinental transport and local/regional emissions representing six modeling years within five decades (1970-2020). We use the CAMx Source Apportionment Technology (OSAT/PSAT) to estimate contributions from 6 source sectors in 7 source regions plus 6 other groups for a total of 48 tagged contributions. On-road mobile sources consistently make the largest U.S. anthropogenic emissions contribution to O3 in all cities examined even though they decline substantially from 1970 to 2005 and also from 2005 to 2020. Off-road mobile source contributions increase from 1970 to 2005 and then decrease after 2005 in all of the cities. The boundary conditions, mostly from intercontinental transport, contribute more than 20 ppb to high maximum daily 8-h average (MDA8) O3 for all six years. We found that lowering NOx emissions raises O3 formation efficiency (OFE) across all emission categories which will limit potential O3 benefits of local NOx strategies in the near future. PM2.5 benefited from adoption of control devices between 1970 and 1980 and has continued to decline through 2005 and expected to decline further by 2020. Area sources such as residential, commercial and fugitive dust emissions stand out as making large contributions to PM2.5 that are not declining. Inter-regional transport is less important in 2020 than 1990 for both pollutants.

Marine Biogeochemistry of Particulate Trace Elements in the Exclusive Economic Zone (eez) of the State of Qatar

Science.gov (United States)

Yigiterhan, O.; Al-Ansari, I. S.; Abdel-Moati, M.; Murray, J. W.; Al-Ansi, M.

2016-02-01

We focus on the trace element geochemistry of particulate matter in the Exclusive Economic Zone (EEZ) of Qatar. A main goal of this research was to analyze a complete suite of trace elements on particulate matter samples from the water column from different oceanographic biogeochemical zones of the EEZ around Qatar. The sample set also includes plankton samples which are the main source of biogenic particles, dust samples which are a source of abiological particles to surface seawater and surface sediments which can be a source of resuspended particles and a sink for settling particles. The 15 metals and 2 non-metals analyzed in this study will be Al, Ti, V, Cd, Co, Cu, Fe, Mn, Ni, Pb, Zn, Mo, Ag, Ba, U and P, N. Many factors control the composition of trace elements in marine particles. Most of these are important in the EEZ of Qatar, including:1. Natural sources: These are rivers, atmospheric dust, sediment resuspension and leaks from oil beds. However, due to very limited rainfall rivers play no major role in Qatar but resuspension of shallow carbonate rich sediments and input of atmospheric dust are important due to strong currents and surrounding deserts.2. Adsorption/desorption: These chemical processes occur everywhere in the ocean and transfer metals between particles and the solution phase.3. Biological uptake: This process is likewise a universal ocean process and results in transport of metals from the solution phase to biological particles.4. Redox conditions: These are important chemical reactions in the oxic, suboxic and anoxic zones. This can be the dominant controlling mechanism in the northeastern hypoxic deeper waters of the Qatar EEZ.5. Anthropogenic sources: The eastern part of the Qatar contains numerous industrial sites, petroleum/gas platforms and refineries. There are numerous industrial sources but the main hot spots are the port of Doha and the industrial cities of Mesaieed, Khor Al-Odaid, and Ras Laffan. We aimed to determine the

Particulate matter characterization of Cauca River water in Colombia

NARCIS (Netherlands)

Gutierrez Marin, Juan Pablo; van Halem, D.; Rietveld, L.C.

2016-01-01

The particulate matter composition in the Upper Cauca River section was studied, considering the importance of this river for the water supply of Cali, Colombia, and the implications that the turbidity of this water source has had for the city's water treatment. Additionally, the upstream Palo River

Particulate matter pollution over a Mediterranean urban area.

Science.gov (United States)

Pateraki, St; Assimakopoulos, V D; Maggos, Th; Fameli, K M; Kotroni, V; Vasilakos, Ch

2013-10-01

The main purpose of this study is to investigate the aerosols' (PM10, PM2.5, and PM1) spatial and temporal distribution in different types of environment in a Mediterranean urban region, the Greater Athens Area based on data from a sampling campaign that took place during the cold and warm period of 2008. The influence of the atmospheric circulation patterns, the possible local transport mechanisms, as well as the differentiation of the PM behaviour from that of the inorganic pollutants (NOx, O3), are analysed and discussed. Furthermore, the Comprehensive Air Quality Model with extensions (CAMx) was applied for selected sampling dates and its results were evaluated against measurements in order to interpret qualitatively the configured picture of the air pollution above the GAA. Analysis of the measurement data show that local sources such as traffic and industry dominate over the prevailing PM loads, especially at the 'hot spot' areas. Moreover, the synoptic circulation patterns associated with calm conditions and southerly flows lead to high particulate pollution levels that also affect the urban background stations. Saharan dust outbreaks appeared to increase the particles' diameter as well as the number of E.U. limit value exceedances within the stations of our network. Without any dependence on the characteristics of the investigated atmosphere, PM1 always constituted the greatest part of the PM2.5 mass while PM10, especially during the Saharan dust episodes, was mainly constituted by the coarse fraction. The numerical modelling approach of the geographical distribution of PM10, PM2.5, NOx and O3 justified the design of the sampling campaign, indicating the need for the systematic and parallel monitoring and modelling of the pollutants' dispersion in order to understand the particulate pollution problem in the GAA and to aid to the formulation of pollution control strategies. Copyright © 2013 Elsevier B.V. All rights reserved.

Validation of NAA Method for Urban Particulate Matter

International Nuclear Information System (INIS)

Woro Yatu Niken Syahfitri; Muhayatun; Diah Dwiana Lestiani; Natalia Adventini

2009-01-01

Nuclear analytical techniques have been applied in many countries for determination of environmental pollutant. Method of NAA (neutron activation analysis) representing one of nuclear analytical technique of that has low detection limits, high specificity, high precision, and accuracy for large majority of naturally occurring elements, and ability of non-destructive and simultaneous determination of multi-elemental, and can handle small sample size (< 1 mg). To ensure quality and reliability of the method, validation are needed to be done. A standard reference material, SRM NIST 1648 Urban Particulate Matter, has been used to validate NAA method. Accuracy and precision test were used as validation parameters. Particulate matter were validated for 18 elements: Ti, I, V, Br, Mn, Na, K, Cl, Cu, Al, As, Fe, Co, Zn, Ag, La, Cr, and Sm,. The result showed that the percent relative standard deviation of the measured elemental concentrations are found to be within ranged from 2 to 14,8% for most of the elements analyzed whereas Hor rat value in range 0,3-1,3. Accuracy test results showed that relative bias ranged from -11,1 to 3,6%. Based on validation results, it can be stated that NAA method is reliable for characterization particulate matter and other similar matrix samples to support air quality monitoring. (author)

Grain Elevators: New Source Performance Standards (NSPS)

Science.gov (United States)

The New Source Performance Standards (NSPS) for Grain Elevators aims to reduce particulate matter pollution. The new amendments seek to clarify definitions, and requirements, as well as propose new regulations on particulate matter emissions

Source apportionment of population representative samples of PM(2.5) in three European cities using structural equation modelling.

Science.gov (United States)

Ilacqua, Vito; Hänninen, Otto; Saarela, Kristina; Katsouyanni, Klea; Künzli, Nino; Jantunen, Matti

2007-10-01

Apportionment of urban particulate matter (PM) to sources is central for air quality management and efficient reduction of the substantial public health risks associated with fine particles (PM(2.5)). Traffic is an important source combustion particles, but also a significant source of resuspended particles that chemically resemble Earth's crust and that are not affected by development of cleaner motor technologies. A substantial fraction of urban ambient PM originates from long-range transport outside the immediate urban environment including secondary particles formed from gaseous emissions of mainly sulphur, nitrogen oxides and ammonia. Most source apportionment studies are based on small number of fixed monitoring sites and capture well population exposures to regional and long-range transported particles. However, concentrations from local sources are very unevenly distributed and the results from such studies are therefore poorly representative of the actual exposures. The current study uses PM(2.5) data observed at population based random sampled residential locations in Athens, Basle and Helsinki with 17 elemental constituents, selected VOCs (xylenes, trimethylbenzenes, nonane and benzene) and light absorbance (black smoke). The major sources identified across the three cities included crustal, salt, long-range transported inorganic and traffic sources. Traffic was associated separately with source categories with crustal (especially Athens and Helsinki) and long-range transported chemical composition (all cities). Remarkably high fractions of the variability of elemental (R(2)>0.6 except for Ca in Basle 0.38) and chemical concentrations (R(2)>0.5 except benzene in Basle 0.22 and nonane in Athens 0.39) are explained by the source factors of an SEM model. The RAINS model that is currently used as the main tool in developing European air quality management policies seems to capture the local urban fraction (the city delta term) quite well, but underestimates

The particulate passage rate, nutrient composition and fermentation characteristics across gastrointestinal tracts in lactating dairy cows fed three different forage source diets.

Science.gov (United States)

Wang, B; Gu, F F; Huang, X B; Liu, J X

2018-04-19

This study was conducted to investigate the particulate passage rate, nutrient characteristics and fermentation parameters across the gastrointestinal tract (GIT) in lactating dairy cows fed cereal straws in comparison with alfalfa hay. Eighteen multiparous Holstein cows were randomly assigned to one of three experimental diets consisting of 55% concentrate, 15% corn silage and 30% different forage sources as follows (% of dry matter [DM]): (i) 23% alfalfa hay and 7% Chinese wild rye hay (AH); (ii) 30% corn stover (CS); and (iii) 30% rice straw (RS). The Cr-mordanted corn silage-neutral detergent fibre was used to estimate the passage flow at week 14. After 14-week feeding, the animals were slaughtered to collect the gastrointestinal digesta. Dietary forage sources had little effect on the fractional passage rates in the rumen (range from 5.05 to 6.25%/hr) or hindgut (range from 4.49 to 5.24%/hr). Total volatile fatty acid (VFA) concentration in the caecum was highest, followed by the rumen, colon and rectum, and the lowest in the abomasum and duodenum, indicating that the large intestines, especially caecum, are the important positions for carbohydrate degradation. Greater proportion of propionate and butyrate and lower acetate were found in the AH compared to CS or RS in colon, but higher acetate in abomasum was found in the cows fed CS or RS compared to AH. In conclusion, cereal straw diets did not change the particulate passage rate in the rumen and hindgut which might be mainly due to the similar DM intake among these three diets. Different forage source diets significantly changed VFA proportion in the abomasum and colon, indicating the existence of different digestion or absorption rates in these tracts among the experimental diets. © 2018 Blackwell Verlag GmbH.

Characteristics of particulate matter emissions from toy cars with electric motors.

Science.gov (United States)

Wang, Xiaofei; Williams, Brent J; Biswas, Pratim

2015-04-01

Aerosol emissions from toy cars with electric motors were characterized. Particle emission rates from the toy cars, as high as 7.47×10(7) particles/s, were measured. This emission rate is lower than other indoor sources such as smoking and cooking. The particles emitted from toy cars are generated from spark discharges inside the electric motors that power the toy cars. Size distribution measurements indicated that most particles were below 100 nm in diameter. Copper was the dominant inorganic species in these particles. By deploying aerosol mass spectrometers, high concentrations of particulate organic matter were also detected and characterized in detail. Several organic compounds were identified using a thermal desorption aerosol gas chromatography. The mass size distribution of particulate organic matter was bimodal. The formation mechanism of particulate organic matter from toy cars was elucidated. A possible new source of indoor air pollution, particles from electric motors in toy cars, was identified. This study characterized aerosol emissions from toy cars in detail. Most of these particles have a diameter less than 100 nm. Copper and some organics are the major components of these particles. Conditions that minimize these emissions were determined.

Revealing transboundary and local air pollutant sources affecting Metro Manila through receptor modeling studies

International Nuclear Information System (INIS)

Pabroa, Preciosa Corazon B.; Bautista VII, Angel T.; Santos, Flora L.; Racho, Joseph Michael D.

2011-01-01

Ambient fine particulate matter (PM 2 .5) levels at the Metro Manila air sampling stations of the Philippine Nuclear Research Research Institute were found to be above the WHO guideline value of 10 μg m 3 indicating, in general, very poor air quality in the area. The elemental components of the fine particulate matter were obtained using the energy-dispersive x-ray fluorescence spectrometry. Positive matrix factorization, a receptor modelling tool, was used to identify and apportion air pollution sources. Location of probable transboundary air pollutants were evaluated using HYSPLIT (Hybrid Single Particle Lagrangian Integrated Trajectory Model) while location of probable local air pollutant sources were determined using the conditional probability function (CPF). Air pollutant sources can either be natural or anthropogenic. This study has shown natural air pollutant sources such as volcanic eruptions from Bulusan volcano in 2006 and from Anatahan volcano in 2005 to have impacted on the region. Fine soils was shown to have originated from China's Mu US Desert some time in 2004. Smoke in the fine fraction in 2006 show indications of coming from forest fires in Sumatra and Borneo. Fine particulate Pb in Valenzuela was shown to be coming from the surrounding area. Many more significant air pollution impacts can be evaluated with the identification of probable air pollutant sources with the use of elemental fingerprints and locating these sources with the use of HYSPLIT and CPF. (author)

Method for determination of stable carbon isotope ratio of methylnitrophenols in atmospheric particulate matter

Directory of Open Access Journals (Sweden)

S. Moukhtar

2011-11-01

Full Text Available A technique for the measurement of the stable isotope ratio of methylnitrophenols in atmospheric particulate matter is presented. Atmospheric samples from rural and suburban areas were collected for evaluation of the procedure. Particulate matter was collected on quartz fibre filters using dichotomous high volume air samplers. Methylnitrophenols were extracted from the filters using acetonitrile. The sample was then purified using a combination of high-performance liquid chromatography and solid phase extraction. The final solution was then divided into two aliquots. To one aliquot, a derivatising agent, Bis(trimethylsilyltrifluoroacetamide, was added for Gas Chromatography-Mass Spectrometry analysis. The second half of the sample was stored in a refrigerator. For samples with concentrations exceeding 1 ng μl⁻¹, the second half of the sample was used for measurement of stable carbon isotope ratios by Gas Chromatography-Isotope Ratio Mass Spectrometry.

The procedure described in this paper provides a method for the analysis of methylnitrophenols in atmospheric particulate matter at concentrations as low as 0.3 pg m⁻³ and for stable isotope ratios with an accuracy of better than ±0.5‰ for concentrations exceeding 100 pg m⁻³.

In all atmospheric particulate matter samples analysed, 2-methyl-4-nitrophenol was found to be the most abundant methylnitrophenol, with concentrations ranging from the low pg m⁻³ range in rural areas to more than 200 pg m⁻³ in some samples from a suburban location.

Behavior of secondary particles in particulate matter collected at eastern Kanagawa

International Nuclear Information System (INIS)

Nishida, Tomohiro; Kikawada, Yoshikazu; Oi, Takao; Honda, Teruyuki

2008-01-01

The suspended particulate matters collected in 100 periods from 2002/10/28 to 2004/10/29 were separated into the water soluble and insoluble components and their main components were analyzed. The characteristics of atmosphere in the east part of Kagawa prefecture and of the secondary particulates were presumed. Therefore, it was considered that in the samples other than Mn the origins of water soluble and insoluble components are different each other from their behavior. The water-soluble part may be mostly ammonium salt (secondary particulate) from the measurement of NH 4 + . Furthermore, it became clear that the evolution of secondary particulate varies largely with season. Then, the variation with season was presumed by the main component analysis using the statistical software, SPSS adding to the correlation coefficient. This method has proved to be effective. (M.H.)

Characteristics of Fine Particulate Carbonaceous Aerosol at Two Remote Sites in Central Asia

Science.gov (United States)

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 ...

Reference volumetric samples of gamma-spectroscopic sources

International Nuclear Information System (INIS)

Taskaev, E.; Taskaeva, M.; Grigorov, T.

1993-01-01

The purpose of this investigation is to determine the requirements for matrices of reference volumetric radiation sources necessary for detector calibration. The first stage of this determination consists in analysing some available organic and nonorganic materials. Different sorts of food, grass, plastics, minerals and building materials have been considered, taking into account the various procedures of their processing (grinding, screening, homogenizing) and their properties (hygroscopy, storage life, resistance to oxidation during gamma sterilization). The procedures of source processing, sample preparation, matrix irradiation and homogenization have been determined. A rotation homogenizing device has been elaborated enabling to homogenize the matrix activity irrespective of the vessel geometry. 33 standard volumetric radioactive sources have been prepared: 14 - on organic matrix and 19 - on nonorganic matrix. (author)

Principal sources and dispersal patterns of suspended particulate matter in nearshore surface waters of the northeast Pacific Ocean and the Hawaiian Islands

Science.gov (United States)

Carlson, P. R. (Principal Investigator); Conomos, T. J.; Janda, R. J.; Peterson, D. H.

1973-01-01

The author has identified the following significant results. ERTS-1 multispectral scanner imagery of the nearshore surface waters of the Northeast Pacific Ocean is proving to be a useful tool for determining source and dispersal of suspended particulate matter. The principal sources of the turbid water, seen best on the green and red bands, are river and stream effluents and actively eroding coastlines; secondary sources are waste effluents and production of planktonic organisms, but these may sometimes be masked by the very turbid plumes of suspended sediment being discharged into the nearshore zone during times of high river discharge. The configuration and distribution of the plumes of turbid water also can be used to infer near-surface current directions. Comparison of imagery of the nearshore water off the northern California coast from October 1972 and January 1973 shows a reversal of the near-surface currents, from predominantly south-setting in the fall (California Current) to north-setting in the winter (Davidson Current).

Analysis of atmospheric particulate matter; application of optical and selected geochemical techniques

Energy Technology Data Exchange (ETDEWEB)

Mastalerz, M.; Glikson, M.; Simpson, R.W. [Indiana University, Bloomington, IN (United States). Indiana Geological Survey

1998-09-01

An increase in particulate matter in the atmosphere has been shown to be linked to increased mortality but this relationship is poorly understood. Light microscopy, electron microscopy, electron microprobe, and micro-FTIR techniques have been applied to study atmospheric particulates in Brisbane, Australia as a part of a study on asthma. The particulate matter samples were collected daily from April to August 1992, and the sampling covered the autumn period which is typically a time of high asthma incidence in Brisbane. Volumetrically, most atmospheric particulate matter is less than 2{mu}m in size. The microscopic analysis reveals that this material is composed mainly of combusted and incompletely burned hydrocarbons from motor vehicle exhaust emissions, quiescent spores of Mucorales, soil bacteria, and inorganic matter in the form of quartz and other silicates. Elemental and functional group analyses confirm microscope identification, documenting carbon-rich, aromatic exhaust material, more aliphatic pollen and spore material and inorganic matter. Fungal spores dominate bioaerosol and are very abundant from the end of April through May to mid-June. The cytoplasmic content of pollens or fungaonly regarded as allergenic. Particulates from the exhaust emissions and crustal material in a sub-micrometer size range may act as carriers or dispersive mechanisms for cytoplasmic material from fungal spores and pollens, perhaps causing periods of the highest exhaust emission to be the most allergenic. 25 refs., 4 figs., 1 tab.

Size-resolved source apportionment of particulate matter in urban Beijing during haze and non-haze episodes

Directory of Open Access Journals (Sweden)

S. L. Tian

2016-01-01

Full Text Available Additional size-resolved chemical information is needed before the physicochemical characteristics and sources of airborne particles can be understood; however, this information remains unavailable in most regions of China due to lacking measurement data. In this study, we report observations of various chemical species in size-segregated particle samples that were collected over 1 year in the urban area of Beijing, a megacity that experiences severe haze episodes. In addition to fine particles, high concentrations of coarse particles were measured during the periods of haze. The abundance and chemical compositions of the particles in this study were temporally and spatially variable, with major contributions from organic matter and secondary inorganic aerosols. The contributions of organic matter to the particle mass decreased from 37.9 to 31.2 %, and the total contribution of sulfate, nitrate and ammonium increased from 19.1 to 33.9 % between non-haze and haze days, respectively. Due to heterogeneous reactions and hygroscopic growth, the peak concentrations of the organic carbon, cadmium and sulfate, nitrate, ammonium, chloride and potassium shifted from 0.43 to 0.65 µm on non-haze days to 0.65–1.1 µm on haze days. Although the size distributions of lead and thallium were similar during the observation period, their concentrations increased by a factor of more than 1.5 on haze days compared with non-haze days. We observed that sulfate and ammonium, which have a size range of 0.43–0.65 µm, sulfate and nitrate, which have a size range of 0.65–1.1 µm, calcium, which has a size range of 5.8–9 µm, and the meteorological factors of relative humidity and wind speed were responsible for haze pollution when the visibility was less than 10 km. Source apportionment using Positive Matrix Factorization showed six PM2.1 sources and seven PM2.1–9 common sources: secondary inorganic aerosol (25.1 % for fine particles vs. 9.8�

Partitioning and source diagnostics of polycyclic aromatic hydrocarbons in rivers in Tianjin, China

International Nuclear Information System (INIS)

Shi, Z.; Tao, S.; Pan, B.; Liu, W.X.; Shen, W.R.

2007-01-01

Water, suspended particulate matter (SPM), and sediment samples were collected from ten rivers in Tianjin and analyzed for 16 polycyclic aromatic hydrocarbons (PAHs), dissolved organic carbon (DOC), particulate organic carbon (POC) in SPM and total organic carbon (TOC) in sediment. The behavior and fate of PAHs influenced by these parameters were examined. Generally, organic carbon was the primary factor controlling the behavior of the 16 PAH species. Partitioning of PAHs between SPM and water phase was studied, and K OC for some PAH species were found to be significantly higher than the predicted values. The source of PAHs contamination was diagnosed by using PAH isomer ratios. Coal combustion was identified to be a long-term and prevailing contamination source for sediment, while sewage/wastewater source could reasonably explain a short-term PAHs contamination of SPM. - Distribution of PAHs among water, suspended solids and sediment was under strong influence of naturally occurring organic carbon

Determination of cobalt in biological samples by line-source and high-resolution continuum source graphite furnace atomic absorption spectrometry using solid sampling or alkaline treatment

International Nuclear Information System (INIS)

Ribeiro, Anderson Schwingel; Vieira, Mariana Antunes; Furtado da Silva, Alessandra; Borges, Daniel L. Gallindo; Welz, Bernhard; Heitmann, Uwe; Curtius, Adilson Jose

2005-01-01

Two procedures for the determination of Co in biological samples by graphite furnace atomic absorption spectrometry (GF AAS) were compared: solid sampling (SS) and alkaline treatment with tetramethylammonium hydroxide (TMAH) using two different instruments for the investigation: a conventional line-source (LS) atomic absorption spectrometer and a prototype high-resolution continuum source atomic absorption spectrometer. For the direct introduction of the solid samples, certified reference materials (CRM) were ground to a particle size ≤50 μm. Alkaline treatment was carried out by placing about 250 mg of the sample in polypropylene flasks, adding 2 mL of 25% m/v tetramethylammonium hydroxide and de-ionized water. Due to its unique capacity of providing a 3-D spectral plot, a high-resolution continuum source (HR-CS) graphite furnace atomic absorption spectrometry was used as a tool to evaluate potential spectral interferences, including background absorption for both sample introduction procedures, revealing that a continuous background preceded the atomic signal for pyrolysis temperatures lower than 700 deg. C. Molecular absorption bands with pronounced rotational fine structure appeared for atomization temperatures >1800 deg. C probably as a consequence of the formation of PO. After optimization had been carried out using high resolution continuum source atomic absorption spectrometry, the optimized conditions were adopted also for line-source atomic absorption spectrometry. Six biological certified reference materials were analyzed, with calibration against aqueous standards, resulting in agreement with the certified values (according to the t-test for a 95% confidence level) and in detection limits as low as 5 ng g -1

Particulate Study on NeoProfen, a Neonatal Injectable Product.

Science.gov (United States)

Krishna, Aravind; Rice, Michael; Kester, Tom; Waters, Michael; Wilson, Terry

2016-01-01

NeoProfen or sterile ibuprofen L-lysine at 10 mg/mL ibuprofen, in 2 mL single-use Type I glass vials is often a first choice medication used to close a patent ductus arteriosus in neonatal patients from 500 to 1500 g body weight. Visible particulate matter was found in vials that were placed on a commercial stability program prior to the approved expiration date of 2 years. A combination of instrumental techniques including inductively coupled plasma-mass spectrometry, x-ray photoelectron spectroscopy, scanning electron microscopy energy dispersive x-ray spectrometry, and Raman and Fourier transform infrared microspectroscopy was used to evaluate stability, pilot batch and packaging samples in a root cause investigation. The particulate matter was shown to consist largely of ibuprofen aluminum salts of various stoichiometries. It developed over time by a substitution mechanism, in which the ibuprofen anion in solution reacts with the aluminum oxide network of the borosilicate glass giving the ibuprofen aluminum salt with =Al-OH remaining in the network. For corrective action an alternate Type I borosilicate glass vial with interior coating, not found in the original vial, was chosen for the product to prevent this occurrence. NeoProfen (sterile preservative-free ibuprofin L-lysine at 17 mg/mL in a single-use glass vial) is used to close a clinically significant patent ductus arteriosus in premature infants no more than 32 weeks gestational age. The neonatal population is especially sensitive to outside chemical, physical and environmental conditions because of incompletely developed organ systems, low birth weight and other underlying conditions. Two batches of this product were voluntarily recalled by the manufacturer, Lundbeck, and investigated for the source of particulate matter observed during a commercial stability testing program. This was found to result from an interaction between the product and the Type I borosilicate glass vial where ibuprofen

Elemental characterization of New Year's Day PM10 and PM2.2 particulates matter at several sites in Metro Manila

Energy Technology Data Exchange (ETDEWEB)

Santos, Flora L; Pabroa, Preciosa Corazon B; Morco, Ryan P; Racho, Joseph Michael D [Analytical Measurements Research Group, Philippine Nuclear Research Institute, Commonwealth Ave., Diliman, Quezon City (Philippines)

2007-07-01

In the Philippines, it has been a yearly tradition to welcome the coming of the New Year with the loudest noise as can be achieved. Firecrackers and fireworks have been a necessity for Filipinos during this time despite bans on the use of most of these and despite the Department of Health (DOH) campaign to use alternative safe practices to welcome the New Year. Data for PM 10 samples (fractionated as PM 10-2.2 or the course fraction and PM2.2 or the fine fraction) collected in four PNRI sampling sites in Metro Manila show the air pollution impacts of fireworks on New Year's Eve. Samples were collected from 1998 to 2006 using a Gent dichotomous sampler in connection with the PNRI project {sup P}articulate Matter Source Apportionment Using Nuclear and Related Analytical Techniques{sup .} Particulate mass was determined by gravimetry. Elemental analysis of the air filters was done using X-ray Fluorescence Spectrometry (X RF) or Particle induced X-ray Emission (PIXE), multielemental non-destructive nuclear analytical techniques. Black carbon was analyzed using reflectometry. PM 10 values increased by two to four times the usual averages (36.4 to 55.4 ug/cum) and in 2002 even exceeded the PNAAQ short-term guideline value of 150 ug/cum at the ADMU sampling station. PM2.2 values increased by two to six times the usual averages (15 to 28 ug/cum), even many times exceeding US EPA short-term guideline value of 65 ug/cum. The increase in the particulate mass of New Year's Day samples can be attributed more to an increase in the metal pollutants rather than the black carbon, with higher contribution to the fine fraction. Increase in the elemental concentrations of Al, S, Cl, K, Ba, Sr, Ti, V, Mn, Cu and Pb were observed with the highest contribution from K. Results show that the usual practices of burning firecrackers and fireworks during New Year's day celebration is a very strong source of air pollution which contributes significantly high amount of metal pollutants in the

Development of a compact powdery sample negative ion source

Energy Technology Data Exchange (ETDEWEB)

Wada, Motoi [Doshisha Univ., Tanabe, Kyoto (Japan). Faculty of Engineering; Sasao, Mamiko; Kawano, Hiroyuki

1997-02-01

A gas-feed-free compact negative ion source can be realized by utilizing the process of electron stimulated desorption from powdery sample. A negative ion source of this type is designed to be attached to a standard 1.33 inch copper-gasket-flange. The ion source is operated stable with LiH powder for more than 10 hours with the mass-separated negative hydrogen ion current of 1 nA. The source causes minute gas emission, and particularly suitable for ion beam applications in which a good vacuum is required. The present status of the compact ion source development is briefly described. (author)

Characterisation of the organic composition of size segregated atmospheric particulate matter at traffic exposed and background sites in Madrid

Science.gov (United States)

Mirante, F.; Perez, R.; Alves, C.; Revuelta, M.; Pio, C.; Artiñano, B.; Nunes, T.

2010-05-01

The growing awareness of the impact of atmospheric particulate matter (PM) on climate, and the incompletely recognised but serious effects of anthropogenic aerosols on air quality and human health, have led to diverse studies involving almost exclusively the coarse or the fine PM fractions. However, these environmental effects, the PM formation processes and the source assignment depend greatly on the particle size distribution. The innovative character of this study consists in obtaining time series with a size-segregated detailed chemical composition of PM for differently polluted sites. In this perspective, a summer sampling campaign was carried out from 1 of June to 1 of July 2009. One of the sampling sites was located at a representative urban monitoring station (Escuelas Aguirre) belonging to the municipal network, located at a heavy traffic street intersection in downtown Madrid. Other sampling point was positioned within the CIEMAT area, located in the NW corner of the city, which can be considered an urban background or suburban site. Particulate matter was sampled with high volume cascade impactors at 4 size stages: 10-2.5, 2.5-0.95, 0.95-0.45 and sources (e.g. vehicular). Carbon preference indices (CPI) close to the unity and the presence of PAHs point out vehicle exhaust as the main emission source of the aliphatic and polycyclic aromatic fractions, especially for the roadside aerosols. Concentration ratios between PAHs were also used to assign emission sources. The abundance and the sources of these carcinogenic pollutants are discussed and compared taking into account the local/regional characteristics. Water-soluble ions in PM were also analysed by ionic chromatography. A portion of the same filters was subjected to metal speciation by Inductively Coupled Plasma Mass Spectrometry (ICP-MS) or Instrumental Neutron Activation Analysis (INAA). Receptor-oriented modelling for source apportionment was applied to the size-segregated PM chemical composition

Nature of suspended particulate matter and concentrations of heavy ...

African Journals Online (AJOL)

The concentrations of metals in bottom sediment in the Tanzanian waters of Lake Victoria and the nature of suspended particulate matter (SPM) were analysed. The objective of the study was to compare levels of metals in sediment from different locations and to establish their sources. Metal concentrations were higher in ...

Influence of Acidification on the Partitioning of Steroid Hormones among Filtrate, Filter Media, and Retained Particulate Matter.

Science.gov (United States)

Havens, Sonya M; Hedman, Curtis J; Hemming, Jocelyn D C; Mieritz, Mark G; Shafer, Martin M; Schauer, James J

2016-09-01

Hormone contamination of aquatic systems has been shown to have deleterious effects on aquatic biota. However, the assessment of hormone contamination of aquatic environments requires a quantitative evaluation of the potential effects of sample preservation on hormone concentrations. This study investigated the influence of acidification (pH 2) of surface water samples on the partitioning of hormones among filtrate, filter media, and filter-retained particulate matter. Hormones were spiked into unpreserved and sulfuric acid-preserved ultrapure water and surface water runoff samples. The samples were filtered, and hormones were extracted from the filter and filtrate and analyzed by high-performance liquid chromatography. Acidification did not influence the partitioning of hormones onto the filter media. For the majority of the hormones investigated in this study, the partitioning of hormones to the filter-retained particulate matter was not influenced by acidification. Acidification increased the partitioning of progesterone and melengestrol acetate onto the retained particulate matter (about 25% for both analytes). Incorporation of an isotopically labeled internal standard (ISTD) for progesterone accounted for the loss of progesterone to the filter-retained particulates and resulted in accurate concentrations of progesterone in the filtrate. The incorporation of an ISTD for melengestrol acetate, however, was unable to account for the loss of melengestrol acetate to the retained particulates and resulted in underestimations of melengestrol acetate in the filtrate. Our results indicate that the analysis of melengestrol acetate in acid preserved surface runoff samples should be conducted on the filter-retained particulates as well as the filtrate. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

Airborne particulate matter from livestock production systems: A review of an air pollution problem

International Nuclear Information System (INIS)

Cambra-Lopez, Maria; Aarnink, Andre J.A.; Zhao Yang; Calvet, Salvador; Torres, Antonio G.

2010-01-01

Livestock housing is an important source of emissions of particulate matter (PM). High concentrations of PM can threaten the environment, as well as the health and welfare of humans and animals. Particulate matter in livestock houses is mainly coarse, primary in origin, and organic; it can adsorb and contain gases, odorous compounds, and micro-organisms, which can enhance its biological effect. Levels of PM in livestock houses are high, influenced by kind of housing and feeding, animal type, and environmental factors. Improved knowledge on particle morphology, primarily size, composition, levels, and the factors influencing these can be useful to identify and quantify sources of PM more accurately, to evaluate their effects, and to propose adequate abatement strategies in livestock houses. This paper reviews the state-of-the-art of PM in and from livestock production systems. Future research to characterize and control PM in livestock houses is discussed. - Control of particulate matter emissions, a major challenge to modern livestock production.

A new sample of faint Gigahertz Peaked Spectrum radio sources

NARCIS (Netherlands)

Snellen, IAG; Schilizzi, RT; de Bruyn, AG; Miley, GK; Rengelink, RB; Rottgering, HJ

The Westerbork Northern Sky Survey (WENSS) has been used to select a sample of Gigahertz Peaked Spectrum (GPS) radio sources at flux densities one to two orders of magnitude lower than bright GPS sources investigated in earlier studies. Sources with inverted spectra at frequencies above 325 MHz have

Source apportionment of particulate matter in Chinese megacities: the implication for emission control strategies

Science.gov (United States)

Huang, Ru-Jin; Elser, Miriam; Wang, Qiyuan Wang; Bozzetti, Carlo; Wolf, Robert; Wang, Yichen; Ni, Haiyan; Wang, Meng; Ho, Kin-Fai; Han, Yongming; Dällenbach, Kaspar; Canonaco, Francesco; Slowik, Jay; El Haddad, Imad; Baltensperger, Urs; Cao, Junji; Prévôt, André S. H.

2015-04-01

The 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. A quantitative understanding of these effects has proven extremely challenging due to spatial and temporal variability in the sources of aerosols and their precursors, the complexity of particle composition, and uncertainties associated with the atmospheric aging of existing particles (Pöschl 2005; Hallquist et al., 2009; Huang et al., 2014). Nowadays the average PM2.5 concentrations in China are approximately one to two orders of magnitude higher than those observed in urban areas in the US and European countries (Cao 2012). This has forced the Chinese government to announce its first national environmental standard for PM2.5 in 2012 and to make highly ambitious plans for emission control. The Chinese aim to reduce the PM2.5 concentrations by up to 25% of the 2012 levels by 2017, backed by 277 billion investments from the central government. To achieve this ambitious aim, a better understanding of the aerosol composition, sources, and atmospheric processing is required. In this study, we present the results from intensive field measurement campaigns carried out in Chinese megacities in 2013/2014. The sources of PM2.5 and the organic aerosol (OA) were investigated by applying the multi-linear engine (ME-2) receptor model (Canonaco et al., 2013) to a comprehensive dataset. Primary sources including vehicle emissions, biomass burning, coal burning, and dust-related emissions were identified and quantified. The contributions from secondary aerosol formation processes to total PM2.5 mass and OA mass were evaluated. Detailed results will be presented and discussed. References Cao, J. J. (2012) J. Earth Environ., 3, 1030

Source apportionment analysis of atmospheric particulates in an industrialised urban site in southwestern Spain

International Nuclear Information System (INIS)

Querol, X.; Alastuey, A.; Sanchez-de-la-Campa, A.; Plana, F.; Ruiz, C.R.; Rosa, J. de la

2002-01-01

A detailed physical and chemical characterisation of total suspended particles (TSP) in the highly industrialised city of Huelva (southwestern Spain) was carried out. The results evidenced a coarse grain-size prevalence (PM 10 accounting for only 40% of TSP mass, 37 and 91 μg/m 3 , respectively). PM 10 levels are in the usual range for urban background sites in Spain. The crustal, anthropogenic and marine components accounted for a mean of a 40%, 24% and 5% of bulk TSP, respectively. As expected from the industrial activities, relatively high PO 4 3- and As levels for an urban site were detected. In addition to the crustal and marine components, source apportionment analysis revealed three additional emission sources influencing the levels and composition of TSP: (a) a petrochemical source, (b) a mixed metallurgical-phosphate source, (c) and an unknown source (Sb and NO 3 - ). Due to the high local emissions, the mean TSP anthropogenic contribution (mostly PM 10 ) obtained for all possible air mass transport scenarios reached 18-29 μg/m 3 . The 2010 annual EU PM 10 limit value (20 μg/m 3 ) would be exceeded by the anthropogenic load recorded for all the air mass transport scenarios, with the exception of the North Atlantic transport (only 15% of the sampling days). Under African air mass transport scenarios (20% of sampling days), the TSP crustal contribution reached near three times the local crustal contribution. It must be pointed out that this crustal input should diminish when sampling PM 10 due to the dominant coarse size distribution of this type of particles. (author)

Particulate carbon and nitrogen determinations in tracer studies: The neglected variables

International Nuclear Information System (INIS)

Collos, Yves; Jauzein, Cécile; Hatey, Elise

2014-01-01

We address two issues in the determination of particulate carbon and nitrogen in suspended matter of aquatic environments. One is the adsorption of dissolved organic matter on filters, leading to overestimate particulate matter. The second is the material loss during filtration due to fragile algal cells breaking up. Examples from both laboratory cultures and natural samples are presented. We recommend using stacked filters in order to estimate the first and filtering different volumes of water in order to evaluate the second. - Highlights: • Adsorption of dissolved organic matter on GF/F filters saturates below 1 ml. • Such adsorption can overestimate (up to 5 fold at low volumes) particulate matter. • Plankton breakage during filtration underestimates (up to 3 fold) particulate matter. • Different volumes should be filtered to detect biases in PC and PN concentrations. • Adsorbed organic carbon is higher in surface ocean than in mid-waters

New approach to measure soil particulate organic matter in intact samples using X-ray computed micro-tomography

Science.gov (United States)

Kravchenko, Alexandra; Negassa, Wakene; Guber, Andrey; Schmidt, Sonja

2014-05-01

Particulate soil organic matter (POM) is biologically and chemically active fraction of soil organic matter. It is a source of many agricultural and ecological benefits, among which are POM's contribution to C sequestration. Most of conventional research methods for studying organic matter dynamics involve measurements conducted on pre-processed i.e., ground and sieved soil samples. Unfortunately, grinding and sieving completely destroys soil structure, the component crucial for soil functioning and C protection. Importance of a better understanding of the role of soil structure and of the physical protection that it provides to soil C cannot be overstated; and analysis of quantities, characteristics, and decomposition rates of POM in soil samples with intact structure is among the key elements of gaining such understanding. However, a marked difficulty hindering the progress in such analyses is a lack of tools for identification and quantitative analysis of POM in intact soil samples. Recent advancement in applications of X-ray computed micro-tomography (μ-CT) to soil science has given an opportunity to conduct such analyses. The objective of the current study is to develop a procedure for identification and quantitative characterization of POM within intact soil samples using X-ray μ-CT images and to test performance of the proposed procedure on a set of multiple intact soil macro-aggregates. We used 16 4-6 mm soil aggregates collected at 0-15 cm depth from a Typic Hapludalf soil at multiple field sites with diverse agricultural management history. The aggregates have been scanned at SIMBIOS Centre, Dundee, Scotland at 10 micron resolution. POM was determined from the aggregate images using the developed procedure. The procedure was based on combining image pre-processing steps with discriminant analysis classification. The first component of the procedure consisted of image pre-processing steps based on the range of gray values (GV) along with shape and size

Tire tread wear particles in ambient air--a previously unknown source of human exposure to the biocide 2-mercaptobenzothiazole.

Science.gov (United States)

Avagyan, Rozanna; Sadiktsis, Ioannis; Bergvall, Christoffer; Westerholm, Roger

2014-10-01

Urban particulate matter (PM), asphalt, and tire samples were investigated for their content of benzothiazole and benzothiazole derivates. The purpose of this study was to examine whether wear particles, i.e., tire tread wear or road surface wear, could contribute to atmospheric concentrations of benzothiazole derivatives. Airborne particulate matter (PM10) sampled at a busy street in Stockholm, Sweden, contained on average 17 pg/m(3) benzothiazole and 64 pg/m(3) 2-mercaptobenzothiazole, and the total suspended particulate-associated benzothiazole and 2-mercaptobenzothiazole concentrations were 199 and 591 pg/m(3), respectively. This indicates that tire tread wear may be a major source of these benzothiazoles to urban air PM in Stockholm. Furthermore, 2-mercaptobenzothiazole was determined in urban air particulates for the first time in this study, and its presence in inhalable PM10 implies that the human exposure to this biocide is underestimated. This calls for a revision of the risk assessments of 2-mercaptobenzothiazole exposure to humans which currently is limited to occupational exposure.

Source apportionment of particulate matter and trace gases near a major refinery near the Houston Ship Channel

Science.gov (United States)

Wallace, Henry W.; Sanchez, Nancy P.; Flynn, James H.; Erickson, Mathew H.; Lefer, Barry L.; Griffin, Robert J.

2018-01-01

From February 7 to 27, 2015, a mobile air quality laboratory was deployed to a location proximate to a major refinery, the Port of Houston, and several neighborhoods to conduct measurements of atmospheric trace gases and particulate matter. Two statistical models were utilized to apportion the sources of pollution impacting this site and the denizens of the nearby neighborhoods. Positive matrix factorization (PMF) was performed on the organic signal of the aerosol mass spectra, resulting in five factors totaling an average of 4.1 μg/m3 of the organic aerosol: hydrocarbon-like (0.67 μg/m3), cooking (0.35 μg/m3) biomass burning (1.14 μg/m3), low-volatility oxidized (1.15 μg/m3), and semi-volatile oxidized (0.78 μg/m3). Principal component analysis was performed on daytime and nighttime data, including concentrations from PMF output, of other PM1 components, and of trace gases. This generated five daytime and five nighttime factors that explained 74.5% and 73.0% of the variance, respectively. The most important factors impacting this site were from mobile source exhaust and petrochemical aromatic compound emissions. Together these two factors also constitute most of the observed carcinogens.

Electrical diesel particulate filter (DPF) regeneration

Science.gov (United States)

Gonze, Eugene V; Ament, Frank

2013-12-31

An exhaust system that processes exhaust generated by an engine includes a diesel particulate filter (DPF) that is disposed downstream of the engine and that filters particulates from the exhaust. An electrical heater is disposed upstream of the DPF and selectively heats the exhaust to initiate combustion of the particulates within the exhaust as it passes therethrough. Heat generated by combustion of the particulates induces combustion of particulates within the DPF.

Elemental concentration of zooplankton and their particulate products

International Nuclear Information System (INIS)

Fowler, S.W.; Oregioni, B.

1974-01-01

Since zooplankton fecal pellets and molts are major vectors in the vertical transport of zinc in the sea, analyses have been made also for other trace metals in these particulate products. Euphausiids and pelagic shrimp were collected live off the Monaco coast by taking several short oblique tows with an Issacs-Kidd midwater trawl. Animals were placed in clean sea water, sorted according to species and immediately transported to the laboratory in plastic containers filled with filtered sea water taken at the collection site. Samples of microplankton, which serve as food for the macroplankton were also taken. Elemental concentrations in whole euphausiids and shrimp were measured. It was observed that molt analyses strongly support the contention that crustacean molts play an important role in the transport of metals and radionuclides in marine ecosystems. Molts can release metals to the water column or sediments upon decomposition or serve as a rich source of metals for organisms of other trophic levels which ingest them

Nicotine Contamination in Particulate Matter Sampling

Directory of Open Access Journals (Sweden)

Eric Garshick

2009-02-01

Full Text Available We have addressed potential contamination of PM2.5 filter samples by nicotine from cigarette smoke. We collected two nicotine samples – one nicotine sampling filter was placed in-line after the collection of PM2.5 and the other stood alone. The overall correlation between the two nicotine filter levels was 0.99. The nicotine collected on the “stand-alone” filter was slightly greater than that on the “in-line” filter (mean difference = 1.10 μg/m3, but the difference was statistically significant only when PM2.5 was low (≤ 50 μg/m3. It is therefore important to account for personal and secondhand smoke exposure while assessing occupational and environmental PM.

Isotopic and Chemical Analysis of Nitrate Sources and Cycling in the San Joaquin River Near Stockton, California

Science.gov (United States)

Silva, S. R.; Kendall, C.; Bemis, B.; Wankel, S.; Bergamaschi, B.; Kratzer, C.; Dileanis, P.; Erickson, D.; Avery, E.; Paxton, K.

2002-12-01

Fish migration through the deep-water channel in the San Joaquin River at Stockton, California is inhibited by low oxygen concentrations during the summer months. The cause for this condition appears to be stagnation and decomposition of algae with attendant oxygen consumption. Algae growth in the San Joaquin River is promoted by nutrients entering the river mainly in the form of nitrate. Possible significant sources of nitrate include soil, fertilizer from agriculture, manure from dairy operations, and N derived from municipal sewage. A 2000 CALFED pilot study investigated the sources and cycling of nitrate at four sites along the San Joaquin River upstream of Stockton using the carbon and nitrogen isotopes of total dissolved and particulate organic matter, together with hydrological measurements and various concentration data, including chlorophyll-a. The nitrate source, its relationship to phytoplankton, and the effect of the nitrate source and cycling on the N isotopic composition of dissolved and particulate organic matter were the primary concerns of the study. The d15N values of dissolved organic nitrogen (DON) were used as a proxy for nitrate d15N because nitrate comprised about 90% of DON. Chlorophyll-a and C:N ratios indicated that the particulate organic matter (POM) consisted largely of plankton and therefore the d15N of POM was used as a proxy for the d15N of plankton. A tentative interpretation of the pilot study was that nitrate was a major nutrient for the plankton and the nitrate was of anthropogenic origin, possibly sewage or animal waste. To test these assumptions and interpretations, we are currently analyzing a set of samples collected in 2001. In addition to the previous sample types, a subset of samples will be measured directly for nitrate d15N to assess the validity of using d15N of DON as a proxy for nitrate.

Characterization of the particulate air pollution in contrasted mega cities

International Nuclear Information System (INIS)

Favez, O.

2008-02-01

This work aims at characterizing the physics and the chemistry that govern particulate air pollution in two mega cities (Paris and Cairo) for which the size distribution and the chemical composition of airborne particles were poorly documented. Seasonal variations of the main aerosol sources and transformation processes are investigated in these two urban centres, with a particular attention to semi-volatile material and secondary organic aerosols. Short-term health effects of Paris size-segregated aerosols, as well as particulate pollution during the Cairo 'Black Cloud' season, are also emphasized here. Finally, the comparison of results obtained for the two mega cities and for another one (Beijing) allows investigating main factors responsible for particulate air pollution in urban centres with contrasted climatic conditions and development levels. Notably, this work also allows the build-up of an experimental dataset which is now available for the modelling of urban air quality and of environmental impacts of mega city air pollution. (author)

Modelisation des emissions de particules microniques et nanometriques en usinage

Science.gov (United States)

Khettabi, Riad

La mise en forme des pieces par usinage emet des particules, de tailles microscopiques et nanometriques, qui peuvent etre dangereuses pour la sante. Le but de ce travail est d'etudier les emissions de ces particules pour fins de prevention et reduction a la source. L'approche retenue est experimentale et theorique, aux deux echelles microscopique et macroscopique. Le travail commence par des essais permettant de determiner les influences du materiau, de l'outil et des parametres d'usinage sur les emissions de particules. E nsuite un nouveau parametre caracterisant les emissions, nomme Dust unit , est developpe et un modele predictif est propose. Ce modele est base sur une nouvelle theorie hybride qui integre les approches energetiques, tribologiques et deformation plastique, et inclut la geometrie de l'outil, les proprietes du materiau, les conditions de coupe et la segmentation des copeaux. Il ete valide au tournage sur quatre materiaux: A16061-T6, AISI1018, AISI4140 et fonte grise.

Spatial and temporal variability of particulate polycyclic aromatic hydrocarbons in Mexico City

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D. A. Thornhill

2008-06-01

Full Text Available As part of the Megacities Initiative: Local and Global Research Observations (MILAGRO study in the Mexico City Metropolitan Area in March 2006, we measured particulate polycyclic aromatic hydrocarbons (PAHs and other gaseous species and particulate properties, including light absorbing carbon or effective black carbon (BC, at six locations throughout the city. The measurements were intended to support the following objectives: to describe spatial and temporal patterns in PAH concentrations, to gain insight into sources and transformations of PAHs and BC, and to quantify the relationships between PAHs and other pollutants. Total particulate PAHs at the Instituto Mexicano del Petróleo (T0 supersite located near downtown averaged 50 ng m⁻³, and aerosol active surface area averaged 80 mm² m⁻³. PAHs were also measured on board the Aerodyne Mobile Laboratory, which visited six sites encompassing a mixture of different land uses and a range of ages of air parcels transported from the city core. A combination of analyses of time series, back trajectories, concentration fields, pollutant ratios, and correlation coefficients supports the concept of T0 as an urban source site, T1 as a receptor site with strong local sources, Pedregal and PEMEX as intermediate sites, Pico Tres Padres as a vertical receptor site, and Santa Ana as a downwind receptor site. Weak intersite correlations suggest that local sources are important and variable and that exposure to PAHs and BC cannot be represented by a single regional-scale value. The relationships between PAHs and other pollutants suggest that a variety of sources and ages of particles are present. Among carbon monoxide, nitrogen oxides (NO_x, and carbon dioxide, particulate PAHs are most strongly correlated with NO_x. Mexico City's PAH/BC mass ratio of 0.01 is similar to that found on a freeway loop in the Los Angeles area and approximately 8–30

Spatial and temporal variability of particulate polycyclic aromatic hydrocarbons in Mexico City

Science.gov (United States)

Thornhill, D. A.; de Foy, B.; Herndon, S. C.; Onasch, T. B.; Wood, E. C.; Zavala, M.; Molina, L. T.; Gaffney, J. S.; Marley, N. A.; Marr, L. C.

2008-06-01

As part of the Megacities Initiative: Local and Global Research Observations (MILAGRO) study in the Mexico City Metropolitan Area in March 2006, we measured particulate polycyclic aromatic hydrocarbons (PAHs) and other gaseous species and particulate properties, including light absorbing carbon or effective black carbon (BC), at six locations throughout the city. The measurements were intended to support the following objectives: to describe spatial and temporal patterns in PAH concentrations, to gain insight into sources and transformations of PAHs and BC, and to quantify the relationships between PAHs and other pollutants. Total particulate PAHs at the Instituto Mexicano del Petróleo (T0 supersite) located near downtown averaged 50 ng m-3, and aerosol active surface area averaged 80 mm2 m-3. PAHs were also measured on board the Aerodyne Mobile Laboratory, which visited six sites encompassing a mixture of different land uses and a range of ages of air parcels transported from the city core. A combination of analyses of time series, back trajectories, concentration fields, pollutant ratios, and correlation coefficients supports the concept of T0 as an urban source site, T1 as a receptor site with strong local sources, Pedregal and PEMEX as intermediate sites, Pico Tres Padres as a vertical receptor site, and Santa Ana as a downwind receptor site. Weak intersite correlations suggest that local sources are important and variable and that exposure to PAHs and BC cannot be represented by a single regional-scale value. The relationships between PAHs and other pollutants suggest that a variety of sources and ages of particles are present. Among carbon monoxide, nitrogen oxides (NOx), and carbon dioxide, particulate PAHs are most strongly correlated with NOx. Mexico City's PAH/BC mass ratio of 0.01 is similar to that found on a freeway loop in the Los Angeles area and approximately 8 30 times higher than that found in other cities. Evidence also suggests that primary

Speciation of 210Po and 210Pb in air particulates determined by sequential extraction

International Nuclear Information System (INIS)

Al-Masri, M.S.; Al-Karfan, K.; Khalili, H.; Hassan, M.

2006-01-01

Speciation of 210 Po and 210 Pb in air particulates of two Syrian phosphate sites with different climate conditions has been studied. The sites are the mines and Tartous port at the Mediterranean Sea. Air filters were collected during September 2000 until February 2002 and extracted chemically using different selective fluids in an attempt to identify the different forms of these two radionuclides. The results have shown that the inorganic and insoluble 21 Po and 21 Pb (attached to silica and soluble in mineral acids) portion was found to be high in both sites and reached a maximum value of 94% and 77% in the mine site and Tartous port site, respectively. In addition, only 24% of 21 Pb in air particulates was found to be associated with organic materials probably produced from the incomplete burning of fuel vehicle and similar activities. Moreover, the 210 Po/ 21- Pb activity ratio in air particulates was higher than that in all samples at both sites and varied between 3.85 in November 2000 at Tartous port site and 20 in April 2001 at the mine area. These activity ratios were also higher than the natural levels. The 210 Po/ 210 Pb activity ratio was also determined in each portion resulting from the selective extraction and found to be higher than that in most samples. The sources of 210 Po excess in these portions are discussed. Soil suspension, which is common in the dry climate dominant in the area, sea water spray and heating of phosphate ores were considered; polonium is more volatile than the lead compounds at even moderate temperature. Furthermore, variations in the chemical forms of 210 Po and 210 Pb during the year were also investigated. However, the results of this study can also be utilized for dose assessment to phosphate industry workers

Speciation of 210Po and 210Pb in air particulates determined by sequential extraction.

Science.gov (United States)

Al-Masri, M S; Al-Karfan, K; Khalili, H; Hassan, M

2006-01-01

Speciation of (210)Po and (210)Pb in air particulates of two Syrian phosphate sites with different climate conditions has been studied. The sites are the mines and Tartous port at the Mediterranean Sea. Air filters were collected during September 2000 until February 2002 and extracted chemically using different selective fluids in an attempt to identify the different forms of these two radionuclides. The results have shown that the inorganic and insoluble (210)Po and (210)Pb (attached to silica and soluble in mineral acids) portion was found to be high in both sites and reached a maximum value of 94% and 77% in the mine site and Tartous port site, respectively. In addition, only 24% of (210)Pb in air particulates was found to be associated with organic materials probably produced from the incomplete burning of fuel vehicle and similar activities. Moreover, the (210)Po/(210)Pb activity ratio in air particulates was higher than that in all samples at both sites and varied between 3.85 in November 2000 at Tartous port site and 20 in April 2001 at the mine area. These activity ratios were also higher than the natural levels. The (210)Po/(210)Pb activity ratio was also determined in each portion resulting from the selective extraction and found to be higher than that in most samples. The sources of (210)Po excess in these portions are discussed. Soil suspension, which is common in the dry climate dominant in the area, sea water spray and heating of phosphate ores were considered; polonium is more volatile than the lead compounds at even moderate temperature. Furthermore, variations in the chemical forms of (210)Po and (210)Pb during the year were also investigated. However, the results of this study can also be utilized for dose assessment to phosphate industry workers.

PIXE analysis of airborne particulate matter from Xalostoc, Mexico: winter to summer comparison

International Nuclear Information System (INIS)

Flores M, J.; Aldape, F.; Diaz, R.V.; Hernandez-Mendez, B.; Garcia G, R.

1999-01-01

A study of elemental contents in airborne particulate matter from the industrial city of Xalostoc, Estado de Mexico, was performed using PIXE. The place has a great variety of industries, it is a heavily populated, and it is a part of Mexico City's conurbation, thus contributing significantly to its atmospheric pollution. At present, there is few information available about elemental contents in airborne particulate matter from that region. In this study, two sets of samples of airborne particulate matter were collected daily during periods of four weeks in summer 1996 and winter 1997; two samples a day, 12 h each, night-time and day-time. Results revealed important information about elemental contents in airborne particulate matter from that area, especially in the respirable fraction PM 2.5 . Comparison of night and day figures showed the presence of some elements such as Cu, Zn, and Pb, attributed, as it was expected, to uninterrupted industrial processes. Appearance of some other elements was more consistent only in either day-time or night-time due to diurnal or nocturnal industrial activities, or produced by human activities such as fuel combustion of automotive vehicles. Comparison of winter to summer results showed some other important features such as higher concentrations of pollutants in winter, because of the dry and cold weather, while summer samples exhibited lower concentrations mainly due to the presence of rain showers

Measurement and analysis of ambient atmospheric particulate matter in urban and remote environments

Science.gov (United States)

Hagler, Gayle S. W.

Atmospheric particulate matter pollution is a challenging environmental concern in both urban and remote locations worldwide. It is intrinsically difficult to control, given numerous anthropogenic and natural sources (e.g. fossil fuel combustion, biomass burning, dust, and seaspray) and atmospheric transport up to thousands of kilometers after production. In urban regions, fine particulate matter (particles with diameters under 2.5 mum) is of special concern for its ability to penetrate the human respiratory system and threaten cardiopulmonary health. A second major impact area is climate, with particulate matter altering Earth's radiative balance through scattering and absorbing solar radiation, modifying cloud properties, and reducing surface reflectivity after deposition in snow-covered regions. While atmospheric particulate matter has been generally well-characterized in populated areas of developed countries, particulate pollution in developing nations and remote regions is relatively unexplored. This thesis characterizes atmospheric particulate matter in locations that represent the extreme ends of the spectrum in terms of air pollution-the rapidly-developing and heavily populated Pearl River Delta Region of China, the pristine and climate-sensitive Greenland Ice Sheet, and a remote site in the Colorado Rocky Mountains. In China, fine particles were studied through a year-long field campaign at seven sites surrounding the Pearl River Delta. Fine particulate matter was analyzed for chemical composition, regional variation, and meteorological impacts. On the Greenland Ice Sheet and in the Colorado Rocky Mountains, the carbonaceous fraction (organic and elemental carbon) of particulate matter was studied in the atmosphere and snow pack. Analyses included quantifying particulate chemical and optical properties, assessing atmospheric transport, and evaluating post-depositional processing of carbonaceous species in snow.

Relationship between indoor and outdoor carbonaceous particulates in roadside households

Energy Technology Data Exchange (ETDEWEB)

Funasaka, K.; Miyazaki, T.; Tsuruho, K. [Osaka City Institute of Public Health and Environmental Sciences (Japan); Tamura, K. [The National Institute for Minamata Disease, Kumamoto (Japan); Mizuno, T. [Mie University (Japan). Dept. of Chemistry for Materials; Kuroda, K. [Osaka City University Medical School (Japan). Dept. of Preventive Medicine and Environmental Health

2000-07-01

Concentrations of particulate matter (PM) and carbonaceous particulates in indoor and outdoor air at roadside private households were measured in Osaka, Japan. The particulate samples were collected on filters using a portable AND sampler capable of separating particles into three different size ranges: over 10 {mu}m, 2-10 {mu}m (coarse) and below 2 {mu}m (fine) in aerodynamic diameter. The filters were weighed and then analyzed for elemental carbon (EC) and organic carbon (OC) by thermal oxidation using a CHN CORDER. The results showed that indoor fine PM concentration is considerably affected by fine EC and the fine EC in indoor air is significantly correlated to that in outdoor air, r = 0.86 (n = 30, p < 0.001). A simple estimation from EC content ratio in diesel exhaust particles indicated that about 30% of indoor particulates of less than 10 {mu}m (PM10) were contributed from diesel exhaust. Additionally, the size characteristics of outdoor PM at roadside and background sites were examined using Andersen Cascade Impactors. (author)

Electrically heated particulate filter restart strategy

Science.gov (United States)

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

2011-07-12

A control system that controls regeneration of a particulate filter is provided. The system generally includes a propagation module that estimates a propagation status of combustion of particulate matter in the particulate filter. A regeneration module controls current to the particulate filter to re-initiate regeneration based on the propagation status.

Control strategies for the reduction of airborne particulate nitrate in California's San Joaquin Valley

Science.gov (United States)

Kleeman, Michael J.; Ying, Qi; Kaduwela, Ajith

The effect of NO x, volatile organic compound (VOC), and NH 3 emissions control programs on the formation of particulate ammonium nitrate in the San Joaquin Valley (SJV) was examined under the typical winter conditions that existed on 4-6 January, 1996. The UCD/CIT photochemical transport model was used for this study so that the source origin of primary particulate matter and secondary particulate matter could be identified. When averaged across the entire SJV, the model results predict that 13-18% of the reactive nitrogen (NO y=NO x+reaction products of NO x) emitted from local sources within the SJV was converted to nitrate at the ground level. Each gram of NO x emitted locally within the SJV (expressed as NO 2) produced 0.23-0.31 g of particulate ammonium nitrate (NH 4NO 3), which is much smaller than the maximum theoretical yield of 1.7 g of NH 4NO 3 per gram of NO 2. The fraction of reactive nitrogen converted to nitrate varied strongly as a function of location. Urban regions with large amounts of fresh NO emissions converted little reactive nitrogen to nitrate, while remote areas had up to 70% conversion (equivalent to approximately 1.2 g of NH 4NO 3 per gram of NO 2). The use of a single spatially averaged ratio of NH 4NO 3/NO x as a predictor of how changes to NO x emissions would affect particulate nitrate concentrations would not be accurate at all locations in the SJV under the conditions studied. The largest local sources of particulate nitrate in the SJV were predicted to be diesel engines and catalyst equipped gasoline engines under the conditions experienced on 6 January, 1996. Together, these sources accounted for less than half of the ground-level nitrate aerosol in the SJV. The remaining fraction of the aerosol nitrate originated from reactive nitrogen originally released upwind of the SJV. The majority of this upwind reactive nitrogen was already transformed to nitrate by the time it entered the SJV. The effect of local emissions controls on

On the Impact of Particulate Matter Distribution on Pressure Drop of Wall-Flow Particulate Filters

Directory of Open Access Journals (Sweden)

Vicente Bermúdez

2017-03-01

Full Text Available Wall-flow particulate filters are a required exhaust aftertreatment system to abate particulate matter emissions and meet current and incoming regulations applying worldwide to new generations of diesel and gasoline internal combustion engines. Despite the high filtration efficiency covering the whole range of emitted particle sizes, the porous substrate constitutes a flow restriction especially relevant as particulate matter, both soot and ash, is collected. The dependence of the resulting pressure drop, and hence the fuel consumption penalty, on the particulate matter distribution along the inlet channels is discussed in this paper taking as reference experimental data obtained in water injection tests before the particulate filter. This technique is demonstrated to reduce the particulate filter pressure drop without negative effects on filtration performance. In order to justify these experimental data, the characteristics of the particulate layer are diagnosed applying modeling techniques. Different soot mass distributions along the inlet channels are analyzed combined with porosity change to assess the new properties after water injection. Their influence on the subsequent soot loading process and regeneration is assessed. The results evidence the main mechanisms of the water injection at the filter inlet to reduce pressure drop and boost the interest for control strategies able to force the re-entrainment of most of the particulate matter towards the inlet channels’ end.

Microfluidic paper-based analytical device for particulate metals.

Science.gov (United States)

Mentele, Mallory M; Cunningham, Josephine; Koehler, Kirsten; Volckens, John; Henry, Charles S

2012-05-15

A microfluidic paper-based analytical device (μPAD) fabricated by wax printing was designed to assess occupational exposure to metal-containing aerosols. This method employs rapid digestion of particulate metals using microliters of acid added directly to a punch taken from an air sampling filter. Punches were then placed on a μPAD, and digested metals were transported to detection reservoirs upon addition of water. These reservoirs contained reagents for colorimetric detection of Fe, Cu, and Ni. Dried buffer components were used to set the optimal pH in each detection reservoir, while precomplexation agents were deposited in the channels between the sample and detection zones to minimize interferences from competing metals. Metal concentrations were quantified from color intensity images using a scanner in conjunction with image processing software. Reproducible, log-linear calibration curves were generated for each metal, with method detection limits ranging from 1.0 to 1.5 μg for each metal (i.e., total mass present on the μPAD). Finally, a standard incineration ash sample was aerosolized, collected on filters, and analyzed for the three metals of interest. Analysis of this collected aerosol sample using a μPAD showed good correlation with known amounts of the metals present in the sample. This technology can provide rapid assessment of particulate metal concentrations at or below current regulatory limits and at dramatically reduced cost.

Simultaneous determination of lead, cadmium and zinc in Metro Manila air particulates by anodic stripping voltammetry

International Nuclear Information System (INIS)

Castaneda, Soledad S.

1999-02-01

Air particulate samples were collected from two monitoring stations in Metro Manila using a 'Gent' type dichotomous sampler for pollutant source apportionment studies. Samples were collected in two fractions: a fine fraction with aerodynamic diameter, d p p 3 : HCL: HF, 4: 1: 1) for at least 20 minutes with subsequent heating at lower power settings for a total of 20 minutes more, effectively decomposed the sample with complete recovery of the elements. The digests were evaporated to near dryness to eliminate the troublesome effect of HF and HNO 3 and to decrease acidity of the electrolytic solution to pH ≥ 2. At pH 2, the addition of at least 0.01 M KCl was needed to improve sensitivity. The formation of Zn-Cu intermetallic compounds which interfered in the accurate quantitation of zinc was eliminated by addition of gallium as a 'third' element. The amount of gallium needed varied from sample to sample and was affected by the pH of the solution. The DPASV parameters found to be optimum for the analysis of the air particulate samples are as follows: pulse amplitude, 50 mV; scan rate, 10 mV/sec; E dep , - 1.30 V; t dep , 2 min; and RDE rotation rate, 1500 rpm. Detection limits of 0.2 ppb for zinc, 0.6 ppb for lead, and 0.05 ppb for cadmium in the sample matrix were obtained. The standard addition method was found to be reliable for the quantitative determination of the analytes in the sample. All R 2 values obtained were > 0.9900 at 95% confidence level. Validation of the established analytical methodology by analyzing certified reference standards and performing parallel analysis by GF-AAS and flame AAS showed acceptable accuracy of the DPASV measurements. (Author)

Particulate hot gas stream cleanup technical issues

Energy Technology Data Exchange (ETDEWEB)

NONE

1998-09-01

This is the tenth in a series of quarterly reports describing the activities performed under Contract No. DE-AC21-94MC31160. Analyses of Hot Gas Stream Cleanup (HGCU) ashes and descriptions of filter performance address aspects of filter operation that are apparently linked to the characteristics of the collected ash or the performance of the ceramic bed filter elements. Task I is designed to generate a data base of the key characteristics of ashes collected from operating advanced particle filters (APFS) and to relate these ash properties to the operation and performance of these filters. Task 2 concerns testing and failure analysis of ceramic filter elements. Under Task I during the past quarter, analyses were performed on a particulate sample from the Transport Reactor Demonstration Unit (TRDU) located at the University of North Dakota Energy and Environmental Research Center. Analyses are in progress on ash samples from the Advanced Particulate Filter (APF) at the Pressurized Fluidized-Bed Combustor (PFBC) that was in operation at Tidd and ash samples from the Pressurized Circulating Fluid Bed (PCFB) system located at Karhula, Finland. A site visit was made to the Power Systems Development Facility (PSDF) to collect ash samples from the filter vessel and to document the condition of the filter vessel with still photographs and videotape. Particulate samples obtained during this visit are currently being analyzed for entry into the Hot Gas Cleanup (HGCU) data base. Preparations are being made for a review meeting on ash bridging to be held at Department of Energy Federal Energy Technology Center - Morgantown (DOE/FETC-MGN) in the near future. Most work on Task 2 was on hold pending receipt of additional funds; however, creep testing of Schumacher FT20 continued. The creep tests on Schumacher FT20 specimens just recently ended and data analysis and comparisons to other data are ongoing. A summary and analysis of these creep results will be sent out shortly. Creep

Considerations for modeling small-particulate impacts from surface coal-mining operations based on wind-tunnel simulations

Energy Technology Data Exchange (ETDEWEB)

Perry, S.G.; Petersen, W.B. [Air Resources Lab., Research Triangle Park, NC (United States); Thompson, R.S. [Atmospheric Research and Exposure Assessment Lab., Research Triangle Park, NC (United States)

1994-12-31

The Clean Air Act Amendments of 1990 provide for a reexamination of the current Environmental Protection Agency`s (USEPA) methods for modeling fugitive particulate (PM10) from open-pit, surface coal mines. The Industrial Source Complex Model (ISCST2) is specifically named as the method that needs further study. Title II, Part B, Section 234 of the Amendments states that {open_quotes}...the Administrator shall analyze the accuracy of such model and emission factors and make revisions as may be necessary to eliminate any significant over-predictions of air quality effect of fugitive particulate emissions from such sources.{close_quotes}

Characterization and source estimation of size-segregated aerosols during 2008-2012 in an urban environment in Beijing

International Nuclear Information System (INIS)

Yu, Lingda; Wang, Guangfu; Zhang, Renjiang

2013-01-01

Full text: During 2008-2012, size-segregated aerosol samples were collected using an eight-stage cascade impactor at Beijing Normal University (BNU) Site, China. These samples were analyzed using particle induced X-ray emission (PIXE) analysis for concentrations of 21 elements consisting of Mg, AI, Si, P, S, CI, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, As, Se, Br, Ba and Pb. The size-resolved data sets were then analyzed using the positive matrix factorization (PMF) technique in order to identify possible sources and estimate their contribution to particulate matter mass. Nine sources were resolved in eight size ranges (025 ∼ 16μm) and included secondary sulphur, motor vehicles, coal combustion; oil combustion, road dust, biomass burning, soil dust, diesel vehicles and metal processing. PMF analysis of size-resolved source contributions showed that natural sources represented by soil dust and road dust contributed about 57% to the predicted primary particulate matter (PM) mass in the coarse size range(>2μm). On the other hand, anthropogenic sources such as secondary sulphur, coal and oil combustion, biomass burning and motor vehicle contributed about 73% in the fine size range <2μm). The diesel vehicles and secondary sulphur source contributed the most in the ultra-fine size range (<0.25μm) and was responsible for about 52% of the primary PM mass. (author)

Characterization and source estimation of size-segregated aerosols during 2008-2012 in an urban environment in Beijing

Energy Technology Data Exchange (ETDEWEB)

Yu, Lingda [Key Laboratory of Beam Technology and Materiais Modification of Ministry of Education, College of Nuclear Science and Technology, Beijing Normal University, Beijing (China); Wang, Guangfu, E-mail: guangfuw@bnu.edu.cn [Beijing Radiation Center, Beijing (China); Zhang, Renjiang [Key Laboratory of Regional Climate-Environment Research for Temperate Eas tAsia (RCE-TEA), Institute of Atmospheric Physics, Chinese Academy of Science, Beijing (China)

2013-07-01

Full text: During 2008-2012, size-segregated aerosol samples were collected using an eight-stage cascade impactor at Beijing Normal University (BNU) Site, China. These samples were analyzed using particle induced X-ray emission (PIXE) analysis for concentrations of 21 elements consisting of Mg, AI, Si, P, S, CI, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, As, Se, Br, Ba and Pb. The size-resolved data sets were then analyzed using the positive matrix factorization (PMF) technique in order to identify possible sources and estimate their contribution to particulate matter mass. Nine sources were resolved in eight size ranges (025 ∼ 16μm) and included secondary sulphur, motor vehicles, coal combustion; oil combustion, road dust, biomass burning, soil dust, diesel vehicles and metal processing. PMF analysis of size-resolved source contributions showed that natural sources represented by soil dust and road dust contributed about 57% to the predicted primary particulate matter (PM) mass in the coarse size range(>2μm). On the other hand, anthropogenic sources such as secondary sulphur, coal and oil combustion, biomass burning and motor vehicle contributed about 73% in the fine size range <2μm). The diesel vehicles and secondary sulphur source contributed the most in the ultra-fine size range (<0.25μm) and was responsible for about 52% of the primary PM mass. (author)

An apparatus for separating and continuously recovering a particulate material carried by a gas stream

International Nuclear Information System (INIS)

Becker, W.R.; Dada, A.G.; Dehollander, W.R.; Sloat, R.J.

1974-01-01

Description is given of an apparatus adapted to separate and recover a particulate material carried by hot corrosive gases. The apparatus comprises a flow-channel connected to a gas stream source carrying a particulate material, a first and second tubes connected to said flow-channel, filtrating devices, recovery containers and flow-restricting valves. This can be applied to the recovery of uranium oxides generated by flame reactions [fr

Historical performance of particulate settleable in a municipality located in the ceramic cluster of Castellón (Spain)

Science.gov (United States)

Pardo, P.; Sanfeliu, Teófilo; Soriano, A.; Pallarés, S.; Vicente, A. B.

2010-05-01

Air pollution can be defined as: "the introduction into the atmosphere by man, directly or indirectly, of substances or energy with have effects deleterious of such a nature that endangers human health, causing damage to biological resources and to ecosystems, which impair material goods and to harm or interfere with amenities and other legitimate uses of the environment". One of the main pollutants in air is the particulate matter. This material particulate includes settleable, particles larger than 10 μm that remain airborne for relatively short periods of time. For what its effects are most pronounced in the vicinity of the emitting sources. The study area is located in the city of Alcora. This population is located in the region eastern of the province of Castellon (Spain). The municipality of Alcora has a high industrial density, highlighting framed companies in chemical industry and non-metallic mineral products. The area has a high traffic density due to the proximity of population to various roads. These two factors point peaks rise high concentration of atmospheric particulate pollutants. The purpose of this paper is conducting a retrospective view of the evolution of settleable particulate concentrations. Settleable particulate samples were collected with a sensor BRITISH STANDARD PS particles during the period between January 2000 and December 2005. 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. Sanfeliu T.; Gómez E.T.; Hernánde D.;Martín J.D.; Ovejero M.; Jordán M.M. (2002). "Avaluation of the particulate atmospheric aerosol in the urban area on Castellón, Spain". Protecction and conservation of the cultural heritage of the Mediterranean cities. Eds. Galán and Zezza Ed. Swets&Zeitlinger, Lisse pp:61-64. Sanfeliu T.; Jordán M.M.; Gómez E

Water-soluble elements in atmospheric particulate matter over tropical and equatorial Atlantic

International Nuclear Information System (INIS)

Buat-Menard, Patrick; Morelli, Jacques; Chesselet, Roger

1974-01-01

Samples of water-soluble atmospheric particulate matter collected from R/V ''Jean Charcot'' (May to October 1971) and R/V ''James Gilliss'' (October 1972) over Tropical and Equatorial Atlantic were analyzed for Na, Mg, K and Ca by atomic absorption and for Cl and S as SO 4 by colorimetry. Data shows a strong geographical dependence of K and Ca enrichment relative to their elemental ratio to Na in sea-water. Ca enrichment is related to presence of identified soluble calcium minerals in continental dust originating from African deserts (Sahara-Kalahari). This dust does not influence amounts of K in the water-soluble phase. When observed, strong K enrichment appears tightly associated with high concentrations of surface-active organic material in the microlayer derived from high biological activity (Gulf of Guinea). Observed in same samples, SO 4 enrichment could also be controlled by the same source. This SO 4 enrichment balances the observed Cl loss in aerosols accordingly with gaseous HCl formation processes in marine atmosphere [fr

Emission factors of particulate matter, polycyclic aromatic hydrocarbons, and levoglucosan from wood combustion in south-central Chile.

Science.gov (United States)

Jimenez, Jorge; Farias, Oscar; Quiroz, Roberto; Yañez, Jorge

2017-07-01

In south-central Chile, wood stoves have been identified as an important source of air pollution in populated areas. Eucalyptus (Eucalyptus globulus), Chilean oak (Nothofagus oblique), and mimosa (Acacia dealbata) were burned in a single-chamber slow-combustion wood stove at a controlled testing facility located at the University of Concepción, Chile. In each experiment, 2.7-3.1 kg of firewood were combusted while continuously monitoring temperature, exhaust gases, burn rate, and collecting particulate matter samples in Teflon filters under isokinetic conditions for polycyclic aromatic hydrocarbon and levoglucosan analyses. Mean particulate matter emission factors were 2.03, 4.06, and 3.84 g/kg dry wood for eucalyptus, oak, and mimosa, respectively. The emission factors were inversely correlated with combustion efficiency. The mean emission factors of the sums of 12 polycyclic aromatic hydrocarbons in particle phases were 1472.5, 2134.0, and 747.5 μg/kg for eucalyptus, oak, and mimosa, respectively. Fluoranthene, pyrene, benzo[a]anthracene, and chrysene were present in the particle phase in higher proportions compared with other polycyclic aromatic hydrocarbons that were analyzed. Mean levoglucosan emission factors were 854.9, 202.3, and 328.0 mg/kg for eucalyptus, oak, and mimosa, respectively. Since the emissions of particulate matter and other pollutants were inversely correlated with combustion efficiency, implementing more efficient technologies would help to reduce air pollutant emissions from wood combustion. Residential wood burning has been identified as a significant source of air pollution in populated areas. Local wood species are combusted for home cooking and heating, which releases several toxic air pollutants, including particulate matter, carbon monoxide, and polycyclic aromatic hydrocarbons. Air pollutant emissions depend on the type of wood and the technology and operational conditions of the wood stove. A better understanding of emissions from

Elemental characterization of inhalable particulate emissions on New Year's day in Metro Manila

Energy Technology Data Exchange (ETDEWEB)

Santos Flora, L; Pabroa, Corazon B; Morco, Ryan P; Racho, Joseph Michael D [Analytical Measurement Research Section, Atomic Research Division, Philippine Nuclear Research Institute, Commonwealth Ave., Diliman, Quezon City (Philippines)

2010-07-01

In the Philippines, it has been a yearly tradition to welcome the coming of the New Year with the loudest noise as can be achieved. Firecrackers and fireworks have been a necessity for Filipinos during this time despite bans on the use of most of these and despite the Department of Health's campaign to use alternative safe practices to welcome the New Year. Data for PM{sub 1}0 samples (fractionated as PM{sub 1}0-2.5 and PM{sub 2}.5) collected from four PNRI sampling sites in Metro Manila show the air pollution impacts of fireworks on New Year's Eve. Samples were collected from 1998 to 2006 using a Gent dichotomous sampler. Particulate mass was determined by gravimetry. Elemental analysis was done using two multi-elemental non-destructive nuclear analytical techniques: X-ray Fluorescence Spectrometry (XRF) and Particle Induced X-ray Emission (PIXE). Black carbon was analyzed using reflectometry. PM{sub 1}0 values increased by two to four times the usual averages (36.4 to 55.4 {mu} m-{sup 3}) and in 2002 even exceeded the PNAAQ short-term guideline value of 150 {mu}g m-{sup 3}), even many times exceeding US EPA short-term guideline value of 35 {mu}g m-{sup 3}. The increase in the particulate mass of New Year's Day samples can be attributed more to an increase in the elemental pollutants rather than the black carbon, with higher contribution from the fine fraction. Increase in the elemental concentrations of A1, S, CI, K, Ba, Sr, Ti, V, Mn, Cu and Pb were observed with the highest contribution from K. Results show that the usual practices of burning firecrackers and fireworks during New Year's Day celebration is a very strong source of air pollution which contributes significantly high amount of elemental pollutants in the air. (author)

Elemental characterization of inhalable particulate emissions on New Year's day in Metro Manila

International Nuclear Information System (INIS)

Santos Flora, L.; Pabroa, Corazon B.; Morco, Ryan P.; Racho, Joseph Michael D.

2010-01-01

In the Philippines, it has been a yearly tradition to welcome the coming of the New Year with the loudest noise as can be achieved. Firecrackers and fireworks have been a necessity for Filipinos during this time despite bans on the use of most of these and despite the Department of Health's campaign to use alternative safe practices to welcome the New Year. Data for PM 1 0 samples (fractionated as PM 1 0-2.5 and PM 2 .5) collected from four PNRI sampling sites in Metro Manila show the air pollution impacts of fireworks on New Year's Eve. Samples were collected from 1998 to 2006 using a Gent dichotomous sampler. Particulate mass was determined by gravimetry. Elemental analysis was done using two multi-elemental non-destructive nuclear analytical techniques: X-ray Fluorescence Spectrometry (XRF) and Particle Induced X-ray Emission (PIXE). Black carbon was analyzed using reflectometry. PM 1 0 values increased by two to four times the usual averages (36.4 to 55.4 μ m- 3 ) and in 2002 even exceeded the PNAAQ short-term guideline value of 150 μg m- 3 ), even many times exceeding US EPA short-term guideline value of 35 μg m- 3 . The increase in the particulate mass of New Year's Day samples can be attributed more to an increase in the elemental pollutants rather than the black carbon, with higher contribution from the fine fraction. Increase in the elemental concentrations of A1, S, CI, K, Ba, Sr, Ti, V, Mn, Cu and Pb were observed with the highest contribution from K. Results show that the usual practices of burning firecrackers and fireworks during New Year's Day celebration is a very strong source of air pollution which contributes significantly high amount of elemental pollutants in the air. (author)

Winter-time size distribution and source apportionment of total suspended particulate matter and associated metals in Delhi

Science.gov (United States)

Srivastava, Arun; Gupta, Sandeep; Jain, V. K.

2009-03-01

A study of the winter time size distribution and source apportionment of total suspended particulate matter (TSPM) and associated heavy metal concentrations have been carried out for the city of Delhi. This study is important from the point of view of implementation of compressed natural gas (CNG) as alternate of diesel fuel in the public transport system in 2001 to reduce the pollution level. TSPM were collected using a five-stage cascade impactor at six sites in the winters of 2005-06. The results of size distribution indicate that a major portion (~ 40%) of TSPM concentration is in the form of PM0.7 (heavy metals associated with various size fractions of TSPM. A very good correlation between coarse and fine size fraction of TSPM was observed. It was also observed that the metals associated with coarse particles have more chances of correlation with other metals; rather they are associated with fine particles. Source apportionment was carried out separately in coarse and fine size modes of TSPM by Chemical Mass Balance Receptor Model (CMB8) as well as by Principle Component Analysis (PCA) of SPSS. Source apportionment by PCA reveals that there are two major sources (possibly vehicular and crustal re-suspension) in both coarse and fine size fractions. Results obtained by CMB8 show the dominance of vehicular pollutants and crustal dust in fine and coarse size mode respectively. Noticeably the dominance of vehicular pollutants are now confined to fine size only whilst during pre CNG era it dominated both coarse and fine size mode. An increase of 42.5, 44.4, 48.2, 38.6 and 38.9% in the concentrations of TSPM, PM10.9, coarse particles, fine particles and lead respectively was observed during pre (2001) to post CNG (2005-06) period.

Nitrogen oxides, ozone and heavy metals analysis of suspended particulate matter (spm) of air in Nairobi, Kenya

International Nuclear Information System (INIS)

Odhiambo, O.; Kinyua, A.M.; Gatebe, C.K.

2001-01-01

Motor vehicle emissions are a major source of air pollution in most urban centers. In Kenya, Nairobi city has the highest traffic density and is therefore a particular cause for concern due to the poor maintenance standards of most vehicles plus the use of leaded gasoline. This study was carried out to determine the levels of nitrogen oxides (nox), suspended particulate matter (PM10), ozone (O3) and heavy metals in the SPM collected from the ambient air of Nairobi city. Sampling was done once every week for a period of three months (February to April 2000). Hourly average concentrations of N0 2 , NO and O3 were measured simultaneously from 9.00 am to 5.00 p.m., at a roundabout connecting two main highways (University and Uhuru) in the city. PM10 was collected using Gent Stacked Filter Unit (SFU) air sampler on nuclepore filters (0.4 and 8.0 ?m pore size for fine and coarse filters respectively) which were weighed and analysed for trace elements by Energy Dispersive X-ray Fluorescent (EDXRF) technique. Nitrogen oxides were analysed with thermo electron's Chemiluminescent nox Model 14B analyser while ozone was by using DASIBI ozone monitor, Model 1003 AH. An automatic vehicle counter was used For determining the vehicle density at the sampling point. The findings of the study show that the values obtained for Pb, Mn, Fe, Br, Zn, Cu and Ca are within the Who guidelines. Lead concentrations ranged from 0.051 to 1.106?g/m3; Fe, 0.149 to 3.154?g/m3; Mn, 0.002 to 0.526?g/m3; Cu, lower limit of detection (LLD) to 0.15?g/m3; Br, LLD to 0.43?g/m3; Zn, LLD to 0.14 ?g/m3 and Ca 2.18 to 5.389?g/m3. Concentrations of NO 2 , NO and O3 were also within the 8-hour Who limits with levels ranging from 0.011-0.976 ppm for NO, 0.001-0.2628 ppm for NO 2 and LLD-0.1258 ppm for ozone. The O3 levels were slightly higher in the afternoons when solar intensity was high especially the days with cloud cover of less than 3 Oktas. PM10 levels were, however, above the Who guidelines for most of

Is there a difference in treatment outcomes between epidural injections with particulate versus non-particulate steroids?

Energy Technology Data Exchange (ETDEWEB)

Bensler, Susanne; Sutter, Reto; Pfirrmann, Christian W.A.; Peterson, Cynthia K. [Orthopedic University Hospital Balgrist, Department of Radiology, Zurich (Switzerland); University of Zurich, Faculty of Medicine, Zurich (Switzerland)

2017-04-15

To compare the outcomes of patients after interlaminar computed tomography (CT)-guided epidural injections of the lumbar spine with particulate vs. non-particulate steroids. 531 consecutive patients were treated with CT-guided lumbar interlaminar epidural injections with steroids and local anaesthetics. 411 patients received a particulate steroid and 120 patients received a non-particulate steroid. Pain levels were assessed using the 11-point numerical rating scale (NRS) and overall reported 'improvement' was assessed using the Patients Global Impression of Change (PGIC) at 1 day, 1 week and 1 month post-injection. Descriptive and inferential statistics were applied. Patients receiving particulate steroids had statistically significantly higher NRS change scores (p = 0.0001 at 1 week; p = 0.0001 at 1 month). A significantly higher proportion of patients receiving particulate steroids reported relevant improvement (PGIC) at both 1 week and 1 month post injection (p = 0.0001) and they were significantly less likely to report worsening at 1 week (p = 0.0001) and 1 month (p = 0.017). Patients treated with particulate steroids had significantly greater pain relief and were much more likely to report clinically relevant overall 'improvement' at 1 week and 1 month compared to the patients treated with non-particulate steroids. (orig.)

Is there a difference in treatment outcomes between epidural injections with particulate versus non-particulate steroids?

International Nuclear Information System (INIS)

Bensler, Susanne; Sutter, Reto; Pfirrmann, Christian W.A.; Peterson, Cynthia K.

2017-01-01

To compare the outcomes of patients after interlaminar computed tomography (CT)-guided epidural injections of the lumbar spine with particulate vs. non-particulate steroids. 531 consecutive patients were treated with CT-guided lumbar interlaminar epidural injections with steroids and local anaesthetics. 411 patients received a particulate steroid and 120 patients received a non-particulate steroid. Pain levels were assessed using the 11-point numerical rating scale (NRS) and overall reported 'improvement' was assessed using the Patients Global Impression of Change (PGIC) at 1 day, 1 week and 1 month post-injection. Descriptive and inferential statistics were applied. Patients receiving particulate steroids had statistically significantly higher NRS change scores (p = 0.0001 at 1 week; p = 0.0001 at 1 month). A significantly higher proportion of patients receiving particulate steroids reported relevant improvement (PGIC) at both 1 week and 1 month post injection (p = 0.0001) and they were significantly less likely to report worsening at 1 week (p = 0.0001) and 1 month (p = 0.017). Patients treated with particulate steroids had significantly greater pain relief and were much more likely to report clinically relevant overall 'improvement' at 1 week and 1 month compared to the patients treated with non-particulate steroids. (orig.)

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.

Science.gov (United States)

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

Modelling of in-stream nitrogen and phosphorus concentrations using different sampling strategies for calibration data

Science.gov (United States)

Jomaa, Seifeddine; Jiang, Sanyuan; Yang, Xiaoqiang; Rode, Michael

2016-04-01

It is known that a good evaluation and prediction of surface water pollution is mainly limited by the monitoring strategy and the capability of the hydrological water quality model to reproduce the internal processes. To this end, a compromise sampling frequency, which can reflect the dynamical behaviour of leached nutrient fluxes responding to changes in land use, agriculture practices and point sources, and appropriate process-based water quality model are required. The objective of this study was to test the identification of hydrological water quality model parameters (nitrogen and phosphorus) under two different monitoring strategies: (1) regular grab-sampling approach and (2) regular grab-sampling with additional monitoring during the hydrological events using automatic samplers. First, the semi-distributed hydrological water quality HYPE (Hydrological Predictions for the Environment) model was successfully calibrated (1994-1998) for discharge (NSE = 0.86), nitrate-N (lowest NSE for nitrate-N load = 0.69), particulate phosphorus and soluble phosphorus in the Selke catchment (463 km2, central Germany) for the period 1994-1998 using regular grab-sampling approach (biweekly to monthly for nitrogen and phosphorus concentrations). Second, the model was successfully validated during the period 1999-2010 for discharge, nitrate-N, particulate-phosphorus and soluble-phosphorus (lowest NSE for soluble phosphorus load = 0.54). Results, showed that when additional sampling during the events with random grab-sampling approach was used (period 2011-2013), the hydrological model could reproduce only the nitrate-N and soluble phosphorus concentrations reasonably well. However, when additional sampling during the hydrological events was considered, the HYPE model could not represent the measured particulate phosphorus. This reflects the importance of suspended sediment during the hydrological events increasing the concentrations of particulate phosphorus. The HYPE model could

Characterization of carbonaceous aerosol emissions from selected combustion sources

International Nuclear Information System (INIS)

Martinez, J.P.G.; Espino, M.P.M.; Pabroa, P.C.B.; Bautista, A.T. VII

2015-01-01

Carbonaceous Particulates are carbon-containing solid or liquid matter which form a significant portion of the fine particulate mass (PM2.5) and these have known profound adverse effects on health, climate and visibility. This study aims to characterize carbonaceous aerosol emissions from different combustion sources to establish fingerprints for these for use in the refinement of improvement of the resolution of sources apportionment studies being done by the Philippine Nuclear Research Institute (PNRI), i.e. to resolve vehicular emission sources. Fine air particulate sample were collected in pre-baked Quartz filters using an improvised collection set-up with a Gent sampler. Concentrations of organic and elemental carbon (OC and EC, respectively) in PM2.5 were measured for the different combustion sources—vehicular emissions, tire pyrolysis, and biomass burning, using a thermal-optical method of analysis following the IMPROVE_A protocol. Measured OC ad EC concentrations are shown as percentages with respect to the total carbon (TC) and are illustrated in a 100% stacked chart. Predominance of the EC2 fraction is exhibited in both the diesel fuelled vehicle and tire pyrolysis emissions with EC2/OC2 ratio distinguishing one from the other, EC2/OC2 is 1.63 and 8.41, respectively. Predominance of either OC2 or OC3 fraction is shown in the unleaded gasoline and LPG Fuelled vehicles and in biomass burning with the OC2/OC3 ratio distinguishing one from the others. OC2/OC3 ratios are 1.33 for unleaded gasoline fuelled vehicle, 1.89 for LPG-fuelled vehicle, 0.55 for biomass burning (leaves) and 0.82 biomass burning (wood). The study has shown probable use of the EC2/OC2 and OC2/OC3 ratios to distinguish fingerprints for combustion sources covered in this study. (author)

40 CFR 86.120-94 - Gas meter or flow instrumentation calibration; particulate, methanol and formaldehyde measurement.

Science.gov (United States)

2010-07-01

... 40 Protection of Environment 18 2010-07-01 2010-07-01 false Gas meter or flow instrumentation... Procedures § 86.120-94 Gas meter or flow instrumentation calibration; particulate, methanol and formaldehyde measurement. (a) Sampling for particulate, methanol and formaldehyde emissions requires the use of gas meters...

Particulate matter (PM 10 ) in Istanbul: Origin, source areas and potential impact on surrounding regions

Science.gov (United States)

Koçak, M.; Theodosi, C.; Zarmpas, P.; Im, U.; Bougiatioti, A.; Yenigun, O.; Mihalopoulos, N.

2011-12-01

Water-soluble ions (Cl -, NO3-, SO42-, CO4-, Na +, NH4+, K +, Mg 2+,Ca 2+), water soluble organic carbon (WSOC), organic and elemental carbon (OC, EC) and trace metals (Al, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Cd and Pb) were measured in aerosol PM 10 samples above the megacity of Istanbul between November 2007 and June 2009. Source apportionment analysis using Positive Matrix Factorization (PMF) indicates that approximately 80% of the PM 10 is anthropogenic in origin (secondary, refuse incineration, fuel oil and solid fuel combustion and traffic). Crustal and sea salt account for 10.2 and 7.5% of the observed mass, respectively. In general, anthropogenic (except secondary) aerosol shows higher concentrations and contributions in winter. Mean concentration and contribution of crustal source is found to be more important during the transitional period due to mineral dust transport from North Africa. During the sampling period, 42 events exceeding the limit value of 50 μg m -3 are identified. A significant percentage (91%; n = 38) of these exceedances is attributed to anthropogenic sources. Potential Source Contribution Function analysis highlights that Istanbul is affected from distant sources from Balkans and Western Europe during winter and from Eastern Europe during summer. On the other hand, Istanbul sources influence western Black Sea and Eastern Europe during winter and Aegean and Levantine Sea during summer.

A possible link between particulate matter air pollution and type 2 diabetes

NARCIS (Netherlands)

Volders, Evelien

2008-01-01

Particulate matter (PM) air pollution is most commonly referred to as PM10 and can be subdivided into coarse particles, fine particles and ultrafine particles. Sources of PM air pollution include combustion from car engines and industrial processes. Expos

Particulate Matter and Black Carbon Concentration Levels in Ashaiman, a Semi-Urban Area of Ghana, 2008

OpenAIRE

Sam-Quarcoo Dotse; Joshua Kwame Asane; F.G. Ofosu

2012-01-01

Particulate matter and black carbon concentration levels in Ashaiman, a semi-urban area of Ghana was assessed. Using IVL PM2.5 and PM10 particle samplers, airborne particulate matter was sampled on Teflon filters for a period of three months. In addition to determination of particulate mass in the two fractions by gravimetrical method, aerosol filters were analyzed to determine Black Carbon (BC) concentration levels using the black smoke method. BC fractions in fine and coarse, together with ...

Externality costs by emission. E. Particulates

International Nuclear Information System (INIS)

Anon.

1991-01-01

Fossil-fuel-fired electricity generating systems, particularly coal and oil-fired facilities, are significant emitters of particulate matter. The major components of particulate emissions from a power plant include ash, which is made up of heavy metals, radioactive isotopes and hydrocarbons, and sulfates (SO 4 ) and nitrates (NO 3 ), which are formed by reaction of sulfur dioxide (SO 2 ) and nitrogen oxides (NO x ) in the atmosphere. The smallest ash particulates (including sulfates and nitrates) cause human respiratory effects and impaired visibility. Other effects may include materials damage due to soiling and possibly corrosion, damage to domestic and wild flora through deposition of particulates on foliage, and possible health effects on domestic animals and wild fauna. Several studies focus on the direct effects of high ambient levels of small particulates. This chapter reviews the available literature on the effects of particulate emissions on humans and their environment, and attempts to assign a cost figure to the environmental effects and human health impairments associated with particulate matter emissions. Specifically, this report focuses on the effects of particulates related to human health, visibility, flora, fauna and materials

Application for airborne particulate matter as a demonstration using k0-NAA method in Dalat nuclear research institute of Vietnam

International Nuclear Information System (INIS)

Ho Manh Dung; Cao Dong Vu; Nguyen Thi Sy; Truong Y; Nguyen Thanh Binh

2004-01-01

The airborne particulate samples have been collected using two types of polycarbonate membrane filter PM 2.5 and PM 2-5-10 in two typical sites of industrial (Ho Chi Minh City) and rural (Dateh) regions in south of Vietnam. The concentration of trace elements in the samples has been determined by the k 0 -NAA procedure developed in Dalat NRI. In order to check the developed k 0 -NAA procedure for the airborne particulate matter, two standard reference materials (SRMs) Urban Particulate NIST-1648 and Vehicle Exhaust Particulates NIES-8 were analyzed and the obtained results have been compared and interpreted in term of deviation between experimental results and the certified values. (author)

Polycyclic aromatic hydrocarbons in the urban atmospheric particulate matter in the city of Naples (Italy)

Science.gov (United States)

Caricchia, Anna Maria; Chiavarini, Salvatore; Pezza, Massimo

An investigation on PAH in the atmospheric particulate matter of the city of Naples has been carried out. Urban atmospheric particulate matter was sampled in three sampling sites (West, East and central areas of the city), whose characteristics were representative of the prevailing conditions. In each site, 24 h samplings for 7 consecutive days were performed during three sampling campaigns, in 1996-1997. The results were comparable with those reported in literature for similar investigations. Total PAH were in the range 2-130 ng m -3, with a seasonal variation (autumn/winter vs. summer) in the range 1.5-4.5. The relative contribution of diesel engines vs. gasoline fuelled engines was evidenced.

Quality-assurance procedures: Method 5G determination of particulate emissions from wood heaters from a dilution tunnel sampling location

Energy Technology Data Exchange (ETDEWEB)

Ward, T.E.; Hartman, M.W.; Olin, R.C.; Rives, G.D.

1989-06-01

Quality-assurance procedures are contained in this comprehensive document intended to be used as an aid for wood-heater manufacturers and testing laboratories in performing particulate matter sampling of wood heaters according to EPA protocol, Method 5G. These procedures may be used in research and development, and as an aid in auditing and certification testing. A detailed, step-by-step quality assurance guide is provided to aid in the procurement and assembly of testing apparatus, to clearly describe the procedures, and to facilitate data collection and reporting. Suggested data sheets are supplied that can be used as an aid for both recordkeeping and certification applications. Throughout the document, activity matrices are provided to serve as a summary reference. Checklists are also supplied that can be used by testing personnel. Finally, for the purposes of ensuring data quality, procedures are outlined for apparatus operation, maintenance, and traceability. These procedures combined with the detailed description of the sampling and analysis protocol will help ensure the accuracy and reliability of Method 5G emission-testing results.

Airborne particulate discriminator

Science.gov (United States)

Creek, Kathryn Louise [San Diego, CA; Castro, Alonso [Santa Fe, NM; Gray, Perry Clayton [Los Alamos, NM

2009-08-11

A method and apparatus for rapid and accurate detection and discrimination of biological, radiological, and chemical particles in air. A suspect aerosol of the target particulates is treated with a taggant aerosol of ultrafine particulates. Coagulation of the taggant and target particles causes a change in fluorescent properties of the cloud, providing an indication of the presence of the target.

Sample preparations for spark source mass spectrography

International Nuclear Information System (INIS)

Catlett, C.W.; Rollins, M.B.; Griffin, E.B.; Dorsey, J.G.

1977-10-01

Methods have been developed for the preparation of various materials for spark source mass spectrography. The essential features of these preparations (all which can provide adequate precision in a cost-effective manner) consist in obtaining spark-stable electrode sample pieces, a common matrix, a reduction of anomolous effects in the spark, the incorporation of a suitable internal standard for plate response normalization, and a reduction in time

Occurrence, characterisation and fate of (nano)particulate Ti and Ag in two Norwegian wastewater treatment plant

DEFF Research Database (Denmark)

Polesel, Fabio; Farkas, Julia; Kjos, Marianne

2018-01-01

was conducted in two full-scale WWTPs in Trondheim (Norway) employing only primary treatment. We assessed the occurrence and elimination of Ti and Ag, and conducted size-based fractionation using sequential filtration of influent samples to separate particulate, colloidal and dissolved fractions. Eight......-hour composite influent samples were collected to assess diurnal variations in total Ti and Ag influx. Measured influent Ti concentrations (up to 290 μg L−1) were significantly higher than Ag (solids (>0.7 μm). Removal efficiencies ≥70% were observed....... Diurnal profiles of influent Ti were correlated to flow and pollutant concentration patterns (especially total suspended solids), with peaks during the morning and/or evening and minima at night, indicating household discharges as predominant source. Irregular profiles were exhibited by influent Ag...

A GIS based estimation of loss of particulate nitrogen and phosphorus in typical drainage area of Pearl River Delta

Science.gov (United States)

Liu, Xiaonan; Wu, Zhifeng; Cheng, Jiong; Liu, Ping

2008-10-01

The output of nitrogen and phosphorus from agricultural activities is the main source for water eutrophication. The fully developed agriculture in vegetables, fruits and flowers in Pearl River Delta gives rise to excessive use of chemical matter such as fertilizer and pesticide and thus bring about the serious water pollution because of the loss of nitrogen (N) and phosphorus (P) from the farmland in the region. Based on Geographic Information System (GIS) and soil pollution data, Universal Soil Loss Equation (USLE) and source type method are used to estimate the loads of particulate N and P from the soil of different land use types in the drainage area of Liuxi River in Guangzhou, China. So the key regions those the NPS pollution occurred can be confirmed and the technical support for the pollution control target and the capital flow concentration can be provided by the results. The study shows that, (1) The total loss of particulate N and P in the drainage area is 582.49 t/a and 424.74 t/a respectively. Among them the loss of particulate N from paddy soil occupies 40.02% and that of forest 6.31%, while the loss of particulate P from the soil of dry-land accounts for 28.75% and that of paddy soil 26.31%. (2) There are significantly different losses of particulate N and P per unit area from the soils of different source land use types in the drainage area. The losses of particulate N and P per unit area are both the highest from the soil of dry-land, which is 7.72 kg/hm2 and 9.50 kg/hm2 respectively, followed by those of orchard, which is 7.20 kg/hm2 and 6.56 kg/hm2 respectively. The causes are excessive use of chemical matter, unreasonable cultivation pattern, and the soil erosion of different land use. (3) The excessive N and P come from the loss of particulate N and P from the fertilization in agricultural production, and they are the main source of the pollutants in Liuxi River water.

Role of dissolved and particulate cadmium in the accumulation of cadmium in cultured oysters (Crassostrea gigas)

Energy Technology Data Exchange (ETDEWEB)

Lekhi, Priyanka [Department of Chemistry, University of British Columbia, Vancouver, BC V6T 1Z4 (Canada)], E-mail: anka.lekhi@ubc.ca; Cassis, D. [Department of Earth and Ocean Sciences, University of British Columbia, Vancouver, BC V6T 1Z4 (Canada); Pearce, C.M. [Pacific Biological Station, Fisheries and Oceans Canada, Nanaimo, BC V9T 6N7 (Canada); Ebell, N. [Odyssey Shellfish Ltd., Nanoose Bay, BC V0R 9G0 (Canada); Maldonado, M.T. [Department of Earth and Ocean Sciences, University of British Columbia, Vancouver, BC V6T 1Z4 (Canada); Orians, K.J. [Department of Chemistry, University of British Columbia, Vancouver, BC V6T 1Z4 (Canada); Department of Earth and Ocean Sciences, University of British Columbia, Vancouver, BC V6T 1Z4 (Canada)

2008-04-15

Pacific oysters (Crassostrea gigas) collected on the coast of British Columbia, Canada have occasionally shown cadmium (Cd) concentrations at or above 2 {mu}g g{sup -1} (wet weight), which has resulted in the loss of some international markets. This study investigated the source and transfer of Cd to oysters by focusing on the role of dissolved and particulate Cd in seawater. Parameters monitored for 1 year at two oyster farm sites on Vancouver Island included: oyster tissue mass and shell length, Cd in oysters, dissolved Cd, particulate Cd, temperature and salinity. Results show that dissolved Cd was the main source of Cd to the oysters and that Cd was mainly concentrated in the gut tissues. A seasonal trend was observed in Cd in oysters, in which levels were lowest during periods of higher temperatures. Results also indicate that the local oceanographic inputs and sediment diagenesis directly affect dissolved Cd and thereby influence the Cd levels in oysters. Particulate matter was not found to be a source of Cd in oysters, and was actually negatively correlated. This was likely due to the uptake of dissolved Cd by phytoplankton and the effect of phytoplankton on oyster tissue mass.

Role of dissolved and particulate cadmium in the accumulation of cadmium in cultured oysters (Crassostrea gigas)

International Nuclear Information System (INIS)

Lekhi, Priyanka; Cassis, D.; Pearce, C.M.; Ebell, N.; Maldonado, M.T.; Orians, K.J.

2008-01-01

Pacific oysters (Crassostrea gigas) collected on the coast of British Columbia, Canada have occasionally shown cadmium (Cd) concentrations at or above 2 μg g -1 (wet weight), which has resulted in the loss of some international markets. This study investigated the source and transfer of Cd to oysters by focusing on the role of dissolved and particulate Cd in seawater. Parameters monitored for 1 year at two oyster farm sites on Vancouver Island included: oyster tissue mass and shell length, Cd in oysters, dissolved Cd, particulate Cd, temperature and salinity. Results show that dissolved Cd was the main source of Cd to the oysters and that Cd was mainly concentrated in the gut tissues. A seasonal trend was observed in Cd in oysters, in which levels were lowest during periods of higher temperatures. Results also indicate that the local oceanographic inputs and sediment diagenesis directly affect dissolved Cd and thereby influence the Cd levels in oysters. Particulate matter was not found to be a source of Cd in oysters, and was actually negatively correlated. This was likely due to the uptake of dissolved Cd by phytoplankton and the effect of phytoplankton on oyster tissue mass

Global chemical composition of ambient fine particulate matter for exposure assessment.

Science.gov (United States)

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

2014-11-18

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/m(3)), secondary inorganic aerosol (11.1 ± 5.0 μg/m(3)), and mineral dust (11.1 ± 7.9 μg/m(3)). Secondary inorganic PM2.5 concentrations exceeded 30 μg/m(3) over East China. Sensitivity simulations suggested that population-weighted ambient PM2.5 from biofuel burning (11 μg/m(3)) could be almost as large as from fossil fuel combustion sources (17 μg/m(3)). These estimates offer information about global population exposure to the chemical components and sources of PM2.5.

Large scale air monitoring: Biological indicators versus air particulate matter

International Nuclear Information System (INIS)

Rossbach, M.; Jayasekera, R.; Kniewald, G.

2000-01-01

Biological indicator organisms are widely used for monitoring and banking purposes since many years. Although the complexity of the interactions between bioorganisms and their environment is generally not easily comprehensible, environmental quality assessment using the bioindicator approach offers some convincing advantages compared to direct analysis of soil, water, or air. Direct measurement of air particulates is restricted to experienced laboratories with access to expensive sampling equipment. Additionally, the amount of material collected generally is just enough for one determination per sampling and no multidimensional characterization might be possible. Further, fluctuations in air masses have a pronounced effect on the results from air filter sampling. Combining the integrating property of bioindicators with the world wide availability and uniform matrix characteristics of air particulates as a prerequisite for global monitoring of air pollution will be discussed. A new approach for sampling urban dust using large volume filtering devices installed in air conditioners of large hotel buildings is assessed. A first experiment was initiated to collect air particulates (300 to 500 g each) from a number of hotels during a period of three to four months by successive vacuum cleaning of used inlet filters from high volume air conditioning installations reflecting average concentrations per three months in different large cities. This approach is expected to be upgraded and applied for global monitoring. Highly positive correlated elements were found in lichen such as K/S, Zn/P, the rare earth elements (REE) and a significant negative correlation between Fig and Cu was observed in these samples. The ratio of concentrations of elements in dust and Usnea spp. is highest for Cr, Zn, and Fe (400-200) and lowest for elements such as Ca, Rb, and Sr (20-10). (author)

The impact of total suspended particulate concentration on workers’ health at ceramic industry

Science.gov (United States)

Sintorini, M. M.

2018-01-01

Ceramic production process pollutes the air with particulate matter at high concentration and has negative impact on the workers. The objective of this research was to determine the particulate concentration in the air and to analyse its impact on the workers. This research used cross sectional method to correlate the particulate concentration, temperature, humidity, smoke level and level of workers’ compliance with safety regulations. Sampling was conducted from April to May 2012 in three locations, i.e. exposure area (Mass Preparation I, II) and non-exposure area (Forming area). In the exposure area (Mass Preparation I and II) where the particulate concentrations were 22.3673 mg/m3 and 14.8277 mg/m3, and 58.33%, the workers had bad health status. In the non-exposure area, where the particulate concentration was 3.2185 mg/m3 and 25% the workers had bad health status. The Odds Ratio among the workers in exposure area was 4.2 times higher than the workers in the non-exposure area.

Investigation and Applications of In-Source Oxidation in Liquid Sampling-Atmospheric Pressure Afterglow Microplasma Ionization (LS-APAG) Source.

Science.gov (United States)

Xie, Xiaobo; Wang, Zhenpeng; Li, Yafeng; Zhan, Lingpeng; Nie, Zongxiu

2017-06-01

A liquid sampling-atmospheric pressure afterglow microplasma ionization (LS-APAG) source is presented for the first time, which is embedded with both electrospray ionization (ESI) and atmospheric pressure afterglow microplasma ionization (APAG) techniques. This ion source is capable of analyzing compounds with diverse molecule weights and polarities. An unseparated mixture sample was detected as a proof-of-concept, giving complementary information (both polarities and non-polarities) with the two ionization modes. It should also be noted that molecular mass can be quickly identified by ESI with clean and simple spectra, while the structure can be directly studied using APAG with in-source oxidation. The ionization/oxidation mechanism and applications of the LS-APAG source have been further explored in the analysis of nonpolar alkanes and unsaturated fatty acids/esters. A unique [M + O - 3H] + was observed in the case of individual alkanes (C 5 -C 19 ) and complex hydrocarbons mixture under optimized conditions. Moreover, branched alkanes generated significant in-source fragments, which could be further applied to the discrimination of isomeric alkanes. The technique also facilitates facile determination of double bond positions in unsaturated fatty acids/esters due to diagnostic fragments (the acid/ester-containing aldehyde and acid oxidation products) generated by on-line ozonolysis in APAG mode. Finally, some examples of in situ APAG analysis by gas sampling and surface sampling were given as well. Graphical Abstract ᅟ.

SPECIEUROPE: The European data base for PM source profiles

OpenAIRE

PERNIGOTTI DENISE; BELIS CLAUDIO; SPANO' LUCA

2015-01-01

A database of atmospheric particulate matter emission source profiles in Europe (SPECIEUROPE) was developed by the Joint Research Center in the framework of the Forum for air quality modeling in Europe (FAIRMODE, Working Group 3). It contains the chemical composition of particulate matter (PM) emission sources reported in the scientific literature and reports drafted by competent authorities. The first release of SPECIEUROPE consists of 151 measured profiles (original), 13 composite (merging ...