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Sample records for atmospheric particulate polycyclic

  1. Source identification of polycyclic aromatic hydrocarbons in fine atmospheric particulates using stable carbon isotopic analysis

    International Nuclear Information System (INIS)

    In this paper, a method is established to quantitatively partition fractional contributions of polycyclic aromatic hydrocarbons (PAHs) in fine atmospheric particulate matters by using stable carbon isotopic analysis. Dichloromethane extraction, TLC purification, and gas chromatography-combustion system and isotope mass spectrometry (GC/C/IRMS), are used to measure the stable carbon isotope compositions (δ13C). The fractional contributions of coal combustion, vehicle exhaust and biomass burning to the PAHs in the fine particulate matters (PM2.5) collected in Jiading district, a suburb of Shanghai, are estimated. The results show that the δ13C values increase with decreasing molecular weight. The coal combustion and biomass burning play bigger role than vehicle exhaust in the PAHs, compared to the δ13C values of PAHs in all kinds of potential pollution sources. The estimated contributions from coal combustion,vehicle exhaust and biomass burning to PAHs of PM2.5 range from 3%- 21%, 29%- 33% and 46%- 67%, respectively, which agree well with the surrounding condition of the sampling site, indicating that it is feasible to estimate the fractional contributions of PAHs quantitatively by using stable carbon isotopic analysis. (authors)

  2. Characterization of particulate polycyclic aromatic hydrocarbons in an urban atmosphere of central-southern Spain.

    Science.gov (United States)

    Villanueva, Florentina; Tapia, Araceli; Cabañas, Beatriz; Martínez, Ernesto; Albaladejo, José

    2015-12-01

    Over 1-year period, 13 polycyclic aromatic hydrocarbons (PAHs) associated with particulate matter PM10 have been monitored for the first time in the atmosphere of Ciudad Real, situated at the central-southern Spain. PM10-bound PAHs were collected using a high-volume sampler from autumn 2012 to summer 2013 and were analyzed by HPLC with fluorescence detector. The most abundant PAHs were pyrene, chrysene, benzo[b]fluoranthene, dibenzo[a,h]anthracene and benzo[g,h,i]perylene. The ∑PAH concentrations in Ciudad Real were 888, 368, 259 and 382 pg m(-3) for winter, spring, summer and autumn seasons, respectively. The diurnal variation of PAH was also investigated presenting the highest concentrations during the evening (19:00-23:00). Benzo[a]pyrene concentrations ranged from 2.4 to 110 pg m(-3), these values are lower than the target value proposed by the European legislation, 1 ng m(-3). Diagnostic ratios were used to identify potential sources of PAHs. Results suggest that vehicle emissions are the major source of identified PAHs, with a higher contribution of diesel engines although other anthropogenic sources could also have an impact on the PAH levels. PMID:26201660

  3. Characterization and risk assessment of polycyclic aromatic hydrocarbons (PAHs) in urban atmospheric Particulate of Tehran, Iran.

    Science.gov (United States)

    Hoseini, Mohammad; Yunesian, Masud; Nabizadeh, Ramin; Yaghmaeian, Kamyar; Ahmadkhaniha, Reza; Rastkari, Noushin; Parmy, Saeid; Faridi, Sasan; Rafiee, Ata; Naddafi, Kazem

    2016-01-01

    In this study, atmospheric concentrations of particulate-bound polycyclic aromatic hydrocarbons (PAHs) in Tehran megacity were determined to investigate the concentration, distribution, and sources of PAHs in PM10. The health risk from exposure to airborne BaPeq through inhalation pathway was also assessed. Toxic equivalency factors (TEFs) approach was used for quantitative risk estimate, and incremental lifetime cancer risk (ILCR) was calculated. PM10 samples were collected at ten sampling locations during the summer 2013 and winter 2014 by using two independent methods of field sampling. The PM10 concentration in winter (89.55 ± 15.56 μg m(-3)) was 1.19 times higher than that in summer (75.42 ± 14.93 μg m(-3)). Sixteen PAHs were measured with the total average concentrations of PAHs ranged from 56.98 ± 15.91 to 110.35 ± 57.31 ng m(-3) in summer and from 125.87 ± 79.02 to 171.25 ± 73.94 ng m(-3) in winter which were much higher than concentrations measured in most similar studies conducted around the world. Molecular diagnostic ratios were used to identify PAH emission sources. The results indicated that gasoline-driven vehicles are the major sources of PAHs in the study area. Risk analysis showed that the mean and 90 % probability estimated inhalation ILCRs were 7.85 × 10(-6) and 16.78 × 10(-6), respectively. Results of a sensitivity analysis indicated that BaP concentration and cancer slope factor (CSF) contributed most to effect on ILCR mean. PMID:26400241

  4. Polycyclic aromatic hydrocarbons and organic matter associated to particulate matter emitted from atmospheric fluidized bed coal combustion

    International Nuclear Information System (INIS)

    The polycyclic aromatic hydrocarbons (PAH) and the organic matter (OM) content associated with particulate matter (PM) emissions from atmospheric fluidized bed coal combustion have been studied. The two main aims of the work have been (a) to study OM and PAH emissions as a function of the coal fluidized bed combustion (FBC) variables in solid phase and (b) to check if there is any correlation between OM and PAH contained in the PM. The combustion was carried out in a laboratory scale plant at different combustion conditions: temperature, percentage of oxygen excess, and total air flow. PAH associated on the particulate matter have been analyzed by fluorescence spectroscopy in the synchronous mode (FS) after PM extraction by sonication with dimethylformamide (DMF). It can be concluded that there is not a direct relationship between the OM content and the PAH supported in the PM emitted. In addition, neither PM or OM show dependence between themselves

  5. Occurrence of gaseous and particulate polycyclic aromatic hydrocarbons in the urban atmosphere: study of sources and ambient temperature effect on the gas/particle concentration and distribution

    Energy Technology Data Exchange (ETDEWEB)

    Tsapakis, Manolis [Environmental Chemical Processes Laboratory (ECPL), Department of Chemistry, University of Crete, EL-71409 Heraklion (Greece); Stephanou, Euripides G. [Environmental Chemical Processes Laboratory (ECPL), Department of Chemistry, University of Crete, EL-71409 Heraklion (Greece)]. E-mail: stephanou@chemistry.uoc.gr

    2005-01-01

    The presence of polycyclic aromatic hydrocarbons (PAHs) in an urban region (Heraklion, Greece) and processes that govern their atmospheric fate were studied from November 2000 until February 2002. Sixteen samples were collected, by using an artifact-free sampling device, on a monthly basis and the concentration of PAHs in gas and particulate phase was determined. The most abundant members (gas + particles) were phenanthrene (20.0 {+-} 7.0 ng m{sup -3}), fluoranthene (6.5 {+-} 1.7 ng m{sup -3}), pyrene (6.6 {+-} 2.4 ng m{sup -3}), and chrysene (3.1 {+-} 1.5 ng m{sup -3}). Total concentration (gas + particulate) of PAH ranged from 44.3 to 129.2 ng m{sup -3}, with a mean concentration of 79.3 ng m{sup -3}. Total concentration of PAHs in gas phase ranged from 31.4 to 84.7 ng m{sup -3} with non-observable seasonal variation. Conversely, maximum PAH concentrations in the particulate phase occurred during winter months. Particulate concentration varied from 11.4 to 44.9 ng m{sup -3}, with an average of 25.2 ng m{sup -3}. PAH distribution between gas and particulate phase was in agreement with the sub-cooled vapor pressure. Shift in gas/particle distribution due to difference in ambient temperature elucidated to some extent the seasonal variation of the concentration of PAHs in particles. - Capsule: Ambient PAH partitioning between gas and particle phases vary between compounds and with environmental conditions.

  6. Atmospheric polycyclic aromatic hydrocarbon profiles and sources in pine needles and particulate matter in Dayton, Ohio, USA

    Science.gov (United States)

    Tomashuk, Timothy A.; Truong, Triet M.; Mantha, Madhavi; McGowin, Audrey E.

    2012-05-01

    Polycyclic aromatic hydrocarbons (PAHs) were measured in pine needles (passive sampling) and on high-volume particulate matter (PM) filters (active sampling) over a period of eight to ten months at two separate sites in the Dayton, Ohio, USA metropolitan area: Moraine and Yellow Springs. Total PAH concentrations for PM ranged from 77.4 μg g-1 to 837 μg g-1 (dry wt.) at both sites with high molecular weight PAHs being the predominant form that tended to be higher in concentration during the colder months. Total PAH concentrations for pine needles varied by tree species and location. With an average concentration of 4187 ng g-1, Austrian pine (Pinus nigra) needles in Moraine ranged from 2543 ng g-1to 6111 ng g-1 (dry wt.) with the lowest and highest concentrations occurring in October and August, respectively. The amount of phenanthrene was extremely high for August, 4200 ± 112, which could have resulted from the close proximity of the tree to the parking lot at a firehouse. White pine (Pinus strobus) needles in Yellow Springs had an average concentration of 384 ng g-1and ranged from 127 ng g-1 to 589 ng g-1 (dry wt.) with September and November, respectively, having the lowest and highest PAH concentrations. The 2- and 3-ring PAHs were the predominant form in P. nigra, while the 4-ring PAHs predominated in P. strobus. Total PAH concentrations in P. nigra were an order of magnitude greater than for P. strobus. A bivariate plot of BaA/(BaA + Chry) versus Flt(Flt + Pyr) allowed the PM and pine needle data to be included in the same source analysis and indicated sources of PM at both sites were biomass and/or coal combustion. This plot also suggested PAHs in Yellow Springs P. strobus originated from petroleum combustion sources, whereas PAHs in Moraine P. nigra originated from petroleum combustion with some sources more aged or remote.

  7. Polycyclic aromatic hydrocarbon adsorption on selected solid particulate matter fractions

    Science.gov (United States)

    Bozek, Frantisek; Huzlik, Jiri; Pawelczyk, Adam; Hoza, Ignac; Naplavova, Magdalena; Jedlicka, Jiri

    2016-02-01

    This article is directed to evaluating the proportion of polycyclic aromatic hydrocarbons (PAHs) captured on particulate matter (PM) classified as PM2.5-10 and PM2.5, i.e. particulate matter of aerodynamic diameter 2.5-10 μm and 2.5 μm. During three week-long and one 2-day campaigns, 22 paired air samples were taken in parallel of PM10 and PM2.5 fractions inside the Mrázovka tunnel in Prague, Czech Republic. Following sample preparation, concentrations of individual PAHs were determined using gas chromatography combined with mass spectrometry. Concentrations of individual pairs of each PAH were tested by the nonparametric method using Spearman's rank correlation coefficient. At significance level p detection limit, where increased measurement error can be expected.

  8. Carbon in Atmospheric Particulate Matter

    International Nuclear Information System (INIS)

    Carbon compounds account for a large fraction of airborne particulate matter ('carbonaceous aerosols'). Their presence raises a number of scientific questions dealing with climate issues and possible effects on human health. This review describes the current state of knowledge with respect to the ambient concentrations levels (elemental carbon, organic carbon and organic matter) and the various emission sources, and summarizes the role of atmospheric carbon in the various environmental issues. The report finishes by identifying the actual gaps in knowledge and gives (related) suggestions for future research

  9. Sorption of polycyclic aromatic hydrocarbons on particulate organic matters

    International Nuclear Information System (INIS)

    Particulate organic matter (POM) is a key organic matter fraction which can influence soil fertility. Its interactions with hydrophobic organic pollutants (HOCs) have not been characterized and the mechanisms of retention of HOCs by POM remain unclear. In the present study, sorption behaviors of polycyclic aromatic hydrocarbons (PAHs) naphthalene (NAP), phenanthrene (PHE), and pyrene (PYR) by POMs separated from different soils were examined and the POMs were characterized by elemental analysis, solid state 13C NMR, and Fourier transform infrared spectroscopy (FT-IR). The results indicated that POMs were mainly composed of aliphatic components with high polarity. The different original POMs showed similar chemical composition and configuration. Sorption behaviors of PAHs indicated that there was no significant difference in sorption capacity among the POMs. Sorption of NAP and PHE by POMs displayed a nonlinear isotherm, while sorption of PYR yielded a linear isotherm. No significant hysteresis and ionic strength effect were observed for PAH desorption from the POMs.

  10. Occurrence and sources of particulate nitro-polycyclic aromatic hydrocarbons in ambient air in Denmark

    DEFF Research Database (Denmark)

    Feilberg, A.; Poulsen, M.W.B.; Nielsen, T.;

    2001-01-01

    The occurrence of selected nitro-polycyclic aromatic hydrocarbons (nitro-PAHs) associated with atmospheric particulate matter has been investigated at an urban site and at a semi-rural site. For this purpose an analysis method based on gas chromatography and tandem ion trap mass spectrometry has...... been developed and applied. The nitro-PAK levels have been compared with levels of other air pollutants including unsubstituted PAHs, inorganic gases and particulate matter, as well as with meteorological parameters. Correlations and concentration ratios suggest that the dominant source of 9...... contribution of the OH initiated formation is estimated to be in the range of 90-100%. However, under wintertime conditions with cloudy weather implying low OH radical production, NO3 radicals may also be important as initiators of nitro-PAH formation. Samples influenced by transport of polluted air masses...

  11. 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. PMID:26681325

  12. Atmospheric polycyclic aromatic hydrocarbons (PAHs) in Asia: A review from 1999 to 2004

    International Nuclear Information System (INIS)

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

  13. Polycyclic aromatic hydrocarbons in atmospheric depositions around the Venice Lagoon

    OpenAIRE

    Rossini, Paolo; Matteucci, Gabriele; Raccanelli, Stefano; Favotto, Maurizio; Guerzoni, Stefano; Gattolin, Massimo

    2007-01-01

    Studies have revealed the potential risks to which human health and ecosystems are exposed in the Venice Lagoon, due to the atmospheric deposition of persistent pollutants such as trace metals and organic compounds. A total of 77 atmospheric bulk deposition samples were collected monthly from April 2002 to December 2004, from three sites located in the cities of Mestre and Venice, and inside the industrial area of Porto Marghera. Samples were analyzed by HRGC/HRMS for polycyclic aromatic hydr...

  14. Particulate matter size distribution and associated polycyclic aromatic hydrocarbon content from indirect and direct injection diesel engines

    Energy Technology Data Exchange (ETDEWEB)

    Collin, F.; Gonnord, M.F. [Ecole Polytechnique, Lab. DCMR, Palaiseau Cedex (France); Momique, J.C.; Monier, R. [PSA Peugeot Citroen, La Garenne-Colombes (France); Walter, Ch. [Association Gradient, Compiegne (France)

    2001-03-28

    Within the framework of atmospheric aerosol study, evaluation of the contribution of the particle source to global atmospheric pollution is a challenge that requires an improvement in the knowledge of particulate matter. As a part of this knowledge improvement, this study has been focused on particles emitted from diesel vehicles. Two light-duty diesel vehicles were studied for particulate matter size distribution and associated polycyclic aromatic hydrocarbon (PAH) content. A diffusional and inertial spectrometer was used, allowing particles from 7.5 nm to 15 {mu}m to be collected and analysed. Teflon-coated glass fibre filters were employed as collector substrates, and weighted prior to and after sampling. Each of them was extracted with methylene chloride in an accelerated solvent extractor, cleaned on a silica gel micro-column and analysed for PAHy by gas chromatography/mass spectrometry using internal standards for quantitation. Both analytical and sampling methods were validated. The highest particle mass was found to be emitted at 0.2 {mu}m for the direct injection engine and 0.07 {mu}m for the indirect injection engine. PAHs were found to be essentially distributed on particles in the accumulation mode, at about 0.2 {mu}m, and high molecular weight PAH distributions were found to be bimodal or trimodal, depending on the engine injection. (Author)

  15. Ten-year Pollution Characteristics of Particulate-associated Polycyclic Aromatic Hydrocarbons in Beijing, China

    Science.gov (United States)

    Zhu, Xianlei; Deng, Changjiang; Biandan, Luobu; Fu, Xianqiang; Mu, Xilong

    2015-04-01

    atmospheric boundary layer (ABL) along with local stagnant condition would lead to severe pollution of PAHs at the study area. Correlation analysis between the concentrations of PAHs with socio-economic status (SES) indicated the significant impacts of population, vehicle fleet and Gross Domestic Products (GDP). With growing vehicle fleet and GDP (indicating ecomonic development) and increasing population (indicating urbanization level), the ΣPAH18 showed an increasing tendency. In the decade covered by the study, China has been optimizing energy structure and implementing policy encouraging more efficient energy use. The remarkable improvement of air quality by the policies, with the data collected in this study, would unfortunatley not be noticed in a short period but could be expected in long-term. Key Words: Polycyclic Aromatic Hydrocarbons; Airborne Particulate Matter; Annual Variation; Source; Socioeconomic status; Beijing Acknowledgments: The study has been supported by Beijing Excellent Talents Project of the year of 2012 (No. 2012D009051000001) and by National Science Foundation (No.41175102)

  16. Exposures to Particulate Matter and Polycyclic Aromatic Hydrocarbons and Oxidative Stress in Schoolchildren

    OpenAIRE

    Bae, Sanghyuk; Pan, Xiao-Chuan; Kim, Su-Young; Park, Kwangsik; Kim, Yoon-Hee; Kim, Ho; Hong, Yun-Chul

    2009-01-01

    Background Air pollution is known to contribute to respiratory and cardiovascular mortality and morbidity. Oxidative stress has been suggested as one of the main mechanisms for these effects on health. Objective The aim of this study was to analyze the effects of exposure to particulate matter (PM) with aerodynamic diameters ≤ 10 μm (PM10) and ≤ 2.5 μm (PM2.5) and polycyclic aromatic hydrocarbons (PAHs) on urinary malondialdehyde (MDA) levels in schoolchildren. Methods The study population co...

  17. Atmospheric particulate pollution in Kenitra (Morocco)

    International Nuclear Information System (INIS)

    Cities of Morocco are exposed to a high atmospheric particulate pollution due to automobile traffic, industrialization, but also to soil dusts (in relation with aridity and desert proximity). Monitoring networks and data about air pollution still rare. The present study is a preliminary work about particulate and heavy metals pollution in Kenitra city. Aerosols had been collected with a PM10 sampler (Partisol), a dichotomous sampler (P M2.5 and P M2.5-10 fractions) and stacked filter unit (Gent type) with a fine fraction (below 2.5 um) and a coarse fraction. In summer, the average PM10 concentration is near 80 u g/N m3, above the EEC rule and OMS recommendations, but similar to some other african towns. The ratio P M2.5/PM 10 is low (below 0.5), with seasonal variation in relation with meteorology. The lead and nickel concentrations are also very low, in relation with the use of leaded gasoline and the oldness of many vehicles. This preliminary work reveals high levels of pollution (especially PM10, Pb and Ni) in the town of Kenitra. The major sources are traffic, soil dusts and resuspension of deposited particles. It is necessary to develop monitoring network and sanitary and and environmental impact studies in these cities

  18. Polycyclic aromatic hydrocarbons and total extractable particulate organic matter in the Arctic aerosol

    International Nuclear Information System (INIS)

    Samples of total suspended particulate matter were collected in March and August 1979 at Barrow, Alaska, a remote site in the Arctic. Ambient concentrations of extractable particulate organic matter (POM), of polycyclic aromatic hydrocarbons (PAH) and of 210Pb were determined. The samples were also examined by optical and scanning electron microscopy. Average concentrations of POM and PAH were similar to those reported for other remote sites in the northern hemisphere, but the concentrations were considerably higher in March than in August. The presence of fly ash in the samples collected during the March sampling period, as well as seasonal differences in the concentrations of the organic species and 210Pb and in meteorology indicate that the principal source of POM and PAH was fossil fuel combustion in the mid-latitudes during the March sampling period. (author)

  19. Role of traffic in atmospheric accumulation of heavy metals and polycyclic aromatic hydrocarbons

    Science.gov (United States)

    Gunawardena, Janaka; Egodawatta, Prasanna; Ayoko, Godwin A.; Goonetilleke, Ashantha

    2012-07-01

    Traffic related emissions have been recognised as one of the main sources of air pollutants. In the research study discussed in this paper, variability of atmospheric total suspended particulate matter (TSP), polycyclic aromatic hydrocarbons (PAH) and heavy metal (HM) concentrations with traffic and land use characteristics during weekdays and weekends were investigated. Data required for the study were collected from a range of sampling sites to ensure a wide mix of traffic and land use characteristics. The analysis undertaken confirmed that zinc has the highest concentration in the atmospheric phase during weekends as well as weekdays. Although the use of leaded gasoline was discontinued a decade ago, lead was the second most commonly detected heavy metal. This is attributed to the association of previously generated lead with roadside soil and re-suspension to the atmosphere. Soil related particles are the primary source of TSP and manganese to the atmosphere. The analysis further revealed that traffic sources are dominant in gas phase PAHs compared to the other sources during weekdays. Land use related sources become important contributors to atmospheric PAHs during weekends when traffic sources are at their minimal levels.

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

    OpenAIRE

    Guillon, A.; Ménach, K.; Flaud, P.-M.; Marchand, N.; H. Budzinski; Villenave, E.

    2013-01-01

    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 ...

  1. Vehicle Traffic as a Source of Particulate Polycyclic Aromatic Hydrocarbon Exposure in the Mexico City Metropolitan Area

    OpenAIRE

    Marr, Linsey C.; GROGAN, LISA A.; Wöhrnschimmel, Henry; MOLINA, LUISAT.; Molina, Mario J.; Smith, Thomas J.; Garshick, Eric

    2004-01-01

    Surface properties of aerosols in the Mexico City metropolitan area have been measured in a variety of exposure scenarios related to vehicle emissions in 2002, using continuous, real-time instruments. The objective of these experiments is to describe ambient and occupational particulate polycyclic aromatic hydrocarbon (PAH) concentrations associated with vehicular traffic and facilities using diesel vehicles. Median total particulate PAH concentrations along Mexico City’s roadways range from ...

  2. Large Abundances of Polycyclic Aromatic Hydrocarbons in Titan's Upper Atmosphere

    Science.gov (United States)

    Lopez-Puertas, M.; Dinelli, B. M.; Adriani, A.; Funke, B.; Garcia-Comas, M.; Moriconi, M. L.; D'Aversa, E.; Boersma, C.; Allamandola, L. J.

    2013-01-01

    In this paper, we analyze the strong unidentified emission near 3.28 micron in Titan's upper daytime atmosphere recently discovered by Dinelli et al.We have studied it by using the NASA Ames PAH IR Spectroscopic Database. The polycyclic aromatic hydrocarbons (PAHs), after absorbing UV solar radiation, are able to emit strongly near 3.3 micron. By using current models for the redistribution of the absorbed UV energy, we have explained the observed spectral feature and have derived the vertical distribution of PAH abundances in Titan's upper atmosphere. PAHs have been found to be present in large concentrations, about (2-3) × 10(exp 4) particles / cubic cm. The identified PAHs have 9-96 carbons, with a concentration-weighted average of 34 carbons. The mean mass is approx 430 u; the mean area is about 0.53 sq. nm; they are formed by 10-11 rings on average, and about one-third of them contain nitrogen atoms. Recently, benzene together with light aromatic species as well as small concentrations of heavy positive and negative ions have been detected in Titan's upper atmosphere. We suggest that the large concentrations of PAHs found here are the neutral counterpart of those positive and negative ions, which hence supports the theory that the origin of Titan main haze layer is located in the upper atmosphere.

  3. Geochemical markers and polycyclic aromatic hydrocarbons in solvent extracts from diesel engine particulate matter.

    Science.gov (United States)

    Fabiańska, Monika; Kozielska, Barbara; Bielaczyc, Piotr; Woodburn, Joseph; Konieczyński, Jan

    2016-04-01

    Exhaust particulate from compression ignition (CI) engines running on engine and chassis dynamometers was studied. Particulate dichloromethane extracts were qualitatively and quantitatively analyzed for polycyclic aromatic hydrocarbons (PAHs) and biomarkers by gas chromatography with flame ionization detector (GC-FID) and gas chromatography-mass spectrometry (GC-MS). PAH group profiles were made and the PAH group shares according to the number of rings (2 or 3; 4; 5 or more) as well as diagnostic indices were calculated. Values of geochemical ratios of selected biomarkers and alkyl aromatic hydrocarbons were compared with literature values. A geochemical interpretation was carried out using these values and biomarker and alkyl aromatic hydrocarbon distributions. It has been shown that geochemical features are unequivocally connected to the emission of fossil fuels and biofuels burned in CI engines. The effect of the exothermic combustion process is limited to low-molecular-weight compounds, which shows that the applied methodology permits source identification of PAHs coexisting in the particulate emitted. PMID:26728284

  4. Chemical Coupling Between Atmospheric Ozone and Particulate Matter

    OpenAIRE

    Meng, Z.; DABDUB, D; Seinfeld, J. H.

    1997-01-01

    A major fraction of ambient particulate matter arises from atmospheric gas-to-particle conversion. Attempts to reduce particulate matter levels require control of the same organic and nitrogen oxide (NO_x) emissions that are precursors to urban and regional ozone formation. Modeling of the gas-aerosol chemical interactions that govern levels of particulate components showed that control of gas-phase organic and NO_x precursors does not lead to proportionate reductions of the gas-phase–derived...

  5. Emission factors of carbonaceous particulate matter and polycyclic aromatic hydrocarbons from residential solid fuel combustions

    Energy Technology Data Exchange (ETDEWEB)

    Shen, Guofeng [Jiangsu Academy of Environmental Science, Nanjing (China). Inst. of Atmospheric Sciences

    2014-07-01

    Emission inventory is basic for the understanding of environmental behaviors and potential effects of compounds, however, current inventories are often associated with relatively high uncertainties. One important reason is the lack of emission factors, especially for the residential solid fuel combustion in developing countries. In the present study, emission factors of a group of pollutants including particulate matter, organic carbon, elemental carbon (sometimes known as black carbon) and polycyclic aromatic hydrocarbons were measured for a variety of residential solid fuels including coal, crop straw, wood, and biomass pellets in rural China. The study provided a large number of emission factors that can be further used in emission estimation. Composition profiles and isomer ratios were investigated and compared so as to be used in source apportionment. In addition, the present study identified and quantified the influence of factors like fuel moisture, volatile matter on emission performance.

  6. Polycyclic aromatic hydrocarbons in atmospheric particles in the metropolitan area of Porto Alegre, Brazil

    Science.gov (United States)

    Dallarosa, Juliana Braga; Mônego, Josiane Garcia; Teixeira, Elba Calesso; Stefens, Josemar Luis; Wiegand, Flávio

    The aim of the present study is to identify and quantify the main sources of polycyclic aromatic hydrocarbons (PAHs) associated with aerosols (PM 10) collected at three different sampling stations: 8° Distrito, CEASA and Charqueadas. The samples were collected between November 2001 and November 2002, and the concentrations of 16 major PAHs were determined according to EPA. The filters containing particulate matter were extracted with dichloromethane in Soxhlet and the extracts were later analysed in a gaseous chromatograph coupled to a mass spectrometer (GS/MS). The average concentrations of PAHs ranged between 0.04 and 2.30 ng m -3. The analysis of principal components was applied to the chemical and meteorological variables in order to facilitate the identification of sources of PAHs emission into the atmospheric particulate. The study identified the following sources of PAHs: vehicular emissions, such as diesel oil, petrol, alcohol, and kerosene; industrial emissions, like lubricating oils; emissions from hospital waste burning, and coal burning at power plants.

  7. Polycyclic aromatic hydrocarbons in atmospheric particles in the metropolitan area of Porto Alegre, Brazil

    Energy Technology Data Exchange (ETDEWEB)

    Dallarosa, J.B.; Monego, J.G.; Teixeira, E.C.; Stefens, J.L.; Wiegand, F. [Fundacao Estadual de Protecao Ambiental, Porto Alegre (Brazil)

    2005-03-01

    The aim of the present study is to identify and quantify the main sources of polycyclic aromatic hydrocarbons (PAHs) associated with aerosols (PM10) collected at three different sampling stations: 8 degrees Distrito, CEASA and Charqueadas. The samples were collected between November 2001 and November 2002, and the concentrations of 16 major PAHs were determined according to EPA. The filters containing particulate matter were extracted with dichloromethane in Soxhlet and the extracts were later analysed in a gaseous chromatograph coupled to a mass spectrometer (GS/MS). The average concentrations of PAHs ranged between 0.04 and 2.30ng m{sup -3}. The analysis of principal components was applied to the chemical and meteorological variables in order to facilitate the identification of sources of PAHs emission into the atmospheric particulate. The study identified the following sources of PAHs: vehicular emissions, such as diesel oil, petrol, alcohol, and kerosene; industrial emissions, like lubricating oils; emissions from hospital waste burning, and coal burning at power plants.

  8. Particulate polycyclic aromatic hydrocarbon spatial variability and aging in Mexico City

    Directory of Open Access Journals (Sweden)

    D. A. Thornhill

    2007-11-01

    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 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 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. Weak intersite correlations suggest that local sources are important and variable and that exposure to PAHs 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-to-black carbon 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. Ratios also indicate that primary combustion particles are rapidly coated by secondary aerosol in Mexico City. If so, the lifetime of PAHs may be prolonged if the coating protects them against photodegradation or heterogeneous reactions.

  9. Particulate polycyclic aromatic hydrocarbon spatial variability and aging in Mexico City

    Science.gov (United States)

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

    2007-11-01

    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 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 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. Weak intersite correlations suggest that local sources are important and variable and that exposure to PAHs 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-to-black carbon 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. Ratios also indicate that primary combustion particles are rapidly coated by secondary aerosol in Mexico City. If so, the lifetime of PAHs may be prolonged if the coating protects them against photodegradation or heterogeneous reactions.

  10. Polycyclic aromatic hydrocarbons and nitropolycyclic aromatic hydrocarbons in particulates emitted by motorcycles

    International Nuclear Information System (INIS)

    We determined eleven PAHs and four NPAHs in particulates and regulated pollutants (CO, CO2, HC, NOx, PM) exhausted from motorcycles to figure out the characteristics of motorcycle exhausts. Fluoranthene and pyrene accounted for more than 50% of the total detected PAHs. Among four detected NPAHs, 6-nitrochrysene and 7-nitrobenz[a]anthracene were the predominant NPAHs and were highly correlated relationship with their parent PAHs (R = 0.93 and 0.97, respectively). The PM and HC emissions tended to be close to the PAH emissions. NOx and NPAHs were negatively correlated. Despite their small engine size, motorcycles emitted much more PM and PAHs, showed stronger PAH-related carcinogenicity and indirect-acting mutagenicity, but weaker NPAH-related direct-acting mutagenic potency than automobiles. This is the first study to analyze both PAHs and NPAHs emitted by motorcycles, which could provide useful information to design the emission regulations and standards for motorcycles such as PM. -- Highlights: ► We characterized PAHs and NPAHs distribution in motorcycle exhausts. ► NPAHs concentrations were about three orders of magnitude lower than those of PAHs. ► We found larger amounts of PM and PAHs in exhaust of motorcycles than of automobiles. ► Motorcycles showed stronger PAH-related toxicity than automobiles. ► Motorcycles showed weaker NPAH-related direct-acting mutagenicity than automobiles. -- Control polycyclic aromatic hydrocarbons and nitropolycyclic aromatic hydrocarbon in particulates emitted by motorcycles due to their toxic potency

  11. Modelling of wet deposition of atmospheric polycyclic aromatic hydrocarbons by the consecutive measurements in an urban area, Japan.

    Science.gov (United States)

    Kojima, Keisuke; Kobayashi, Shinji; Kindaichi, Tomonori; Ozaki, Noriatsu

    2010-01-01

    The wet deposition for particulate matter (PM) and polycyclic aromatic hydrocarbons (PAHs) was modelled from the consecutive measurements of atmospheric concentration and wet deposition for particulate matter and PAHs in Higashi-Hiroshima city, Japan. In order to estimate the model in detail, the wet deposition was classified with that from gaseous and PM phase. The gaseous PAHs assumed to be dissolved into raindrops according to Henry's constant, and the PAHs attached on atmospheric PM were assumed to be trapped with PM. The PM was classified with coarse (>7 μm) and fine (0.6-7 μm) PM for the calculation of trap. PM and PAHs depositions estimated with the wet deposition model were compared with measured data. The ratios of the measured to the estimated values of PM and PAHs gave close agreement with measurements (0.41-4.29 (1.35: average) for PM and (0.32-3.83 (1.42)) for PAHs) regardless of precipitation. The depositions of PAHs of liquid and particulate phase were on the other hand significantly different from those from gaseous and PM phases respectively. From those differences, the transfer from particulate to liquid phase was suggested to occur during the precipitation. PMID:20962409

  12. Atmospheric polycyclic aromatic hydrocarbons and isomer ratios as tracers of biomass burning emissions in Northern India.

    Science.gov (United States)

    Rajput, Prashant; Sarin, M M; Sharma, Deepti; Singh, Darshan

    2014-04-01

    Emission from large-scale post-harvest agricultural-waste burning (paddy-residue burning during October-November and wheat-residue burning in April-May) is a conspicuous feature in northern India. The poor and open burning of agricultural residue result in massive emission of carbonaceous aerosols and organic pollutants to the atmosphere. In this context, concentrations of atmospheric polycyclic aromatic hydrocarbons (PAHs) and their isomer ratios have been studied for a 2-year period from a source region (Patiala: 30.2°N; 76.3°E) of two distinct biomass burning emissions. The concentrations of 4-6 ring PAHs are considerably higher compared to 2-3 ring PAHs in the ambient particulate matter (PM2.5). The crossplots of PAH isomer ratios, fluoranthene / (fluoranthene + pyrene) and indeno[1,2,3-cd]pyrene/(indeno[1,2,3-cd]pyrene + benzo[g,h,i]perylene) for two biomass burning emissions, exhibit distinctly different source characteristics compared to those for fossil-fuel combustion sources in south and south-east Asia. The PAH isomer ratios studied from different geographical locations in northern India also exhibit similar characteristics on the crossplot, suggesting their usefulness as diagnostic tracers of biomass burning emissions. PMID:24442960

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

    Directory of Open Access Journals (Sweden)

    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 (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

  14. 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

  15. Characteristics of particulate-bound polycyclic aromatic hydrocarbons emitted from industrial grade biomass boilers.

    Science.gov (United States)

    Yang, Xiaoyang; Geng, Chunmei; Sun, Xuesong; Yang, Wen; Wang, Xinhua; Chen, Jianhua

    2016-02-01

    Polycyclic aromatic hydrocarbons (PAHs) are carcinogenic or mutagenic and are important toxic pollutants in the flue gas of boilers. Two industrial grade biomass boilers were selected to investigate the characteristics of particulate-bound PAHs: one biomass boiler retro-fitted from an oil boiler (BB1) and one specially designed (BB2) biomass boiler. One coal-fired boiler was also selected for comparison. By using a dilution tunnel system, particulate samples from boilers were collected and 10 PAH species were analyzed by gas chromatography-mass spectrometry (GC-MS). The total emission factors (EFs) of PAHs ranged from 0.0064 to 0.0380mg/kg, with an average of 0.0225mg/kg, for the biomass boiler emission samples. The total PAH EFs for the tested coal-fired boiler were 1.8 times lower than the average value of the biomass boilers. The PAH diagnostic ratios for wood pellets and straw pellets were similar. The ratio of indeno(1,2,3-cd)pyrene/[indeno(1,2,3-cd)pyrene+benzo(g,h,i)perylene] for the two biomass boilers was lower than those of the reference data for other burning devices, which can probably be used as an indicator to distinguish the emission of biomass boilers from that of industrial coal-fired boilers and residential stoves. The toxic potential of the emission from wood pellet burning was higher than that from straw pellet burning, however both of them were much lower than residential stove exhausts. PMID:26969542

  16. Nitro Polycyclic Aromatic Hydrocarbons in Particulate Matter Emitted by the Combustion of Diesel and Biodiesel

    Science.gov (United States)

    Valle-Hernández, B. L.; Amador-Muñoz, O.; Jazcilevich, A. D.; Santos-Medina, G. L.; Hernández-Lopéz, E.; Villalobos-Pietrini, R.

    2013-05-01

    The rapid population growth in large urban areas, has resulted in a precipitous increase in the consumption of fossil fuels, mainly by the transport sector, diesel vehicles are a significant source of air pollution by particulate matter emissions, damaging the population health, because of the size and composition of these particles, as they may contain carcinogenic organic compounds such as polycyclic aromatic hydrocarbons and their derivatives, nitro-PAH. This study focused on analysis of nitro-PAH contained in particles emitted from diesel engines fuelled with biodiesel blends (B5, B10 and B16.67) to different driving cycles (rpm and torque), and to compare their concentrations with emissions from current diesel. A diesel truck engine was used in the laboratory for collect particulate mass emitted directly from the exhaust. Mass of particles and nitro-PAH were determined by gas chromatography-mass spectrometry using negative chemical ionization. No reduction was observed in the particles mass per second by using biodiesel relative to diesel (p > 0.1). Seven nitro-PAH were observed in samples: 1-nitronaphthalene, 2-nitronaphthalene, 9-nitroanthracene, 3-nitrophenanthrene, 1,8-dinitronaphthalene, 1-nitropyrene and 1,6-dinitropyrene. 1-nitropyrene showed the highest mass concentration in diesel and in all blends of biodiesel, followed by 3-nitrophenanthrene. Emissions reduction in biodiesel combustion with respect to diesel combustion were observed for 1-nitropyrene: 50 %, in all blends (B5, B10 and B16.67) and for 3-nitrophenanthrene: 55 % in B5, 72 % in B10 and 64 % in B16.67.

  17. 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 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) concentration provide a better estimation of carcinogenicity activities; health risk to adults and children associated with PAHs inhalation was assessed by taking into account the lifetime average daily dose and corresponding incremental lifetime cancer risk (ILCR). The ILCR was within the acceptable range (10-6-10-4), indicating a low health risk to residents in these areas.

  18. Semi-Volatile and Particulate Polycyclic Aromatic Hydrocarbons inEnvironmental Tobacco Smoke: Cleanup, Speciation and EmissionsFactors

    Energy Technology Data Exchange (ETDEWEB)

    Gundel, L.A.; Mahanama, K.R.R.; Daisey, J.M.

    1995-02-01

    Studies of phase distributions and emission factors for polycyclic aromatic hydrocarbons (PAH) in environmental tobacco smoke (ETS) require collection and analysis of very small samples. To achieve the necessary selectivity and sensitivity, a method has been devised and tested for extraction and cleanup of gas- and particulate-phase ETS samples. Gas-phase species were trapped by polymeric sorbents, and particles were trapped on filters. The samples were extracted with hot cyclohexane, concentrated and passed through silica solid-phase extraction columns for cleanup. After solvent change, the PAH were determined by high performance liquid chromatography with two programmed fluorescence detectors. PAH concentrations in 15-mg aliquots of National Institute of Standards and Technology Standard Reference Material SRM 1649 (Urban DustIOrganics) agreed well with published values. Relative precision at the 95% confidence level was 8% for SRM 1649 and 20% for replicate samples (5 mg) of ETS particles. Emission factors have been measured for a range of gas- and particulate-phase polycyclic aromatic hydrocarbons in ETS. The emission factors per cigarette were 13.0{+-}0.5 mg particulate matter, 11.2{+-}0.9 pg for gas-phase naphthalene and 74{+-}10 {micro}g for particulate benzo(a)pyrene.

  19. PAHs concentration and toxicity in organic solvent extracts of atmospheric particulate matter and sea sediments.

    Science.gov (United States)

    Ozaki, Noriatsu; Takeuchi, Shin-ya; Kojima, Keisuke; Kindaichi, Tomonori; Komatsu, Toshiko; Fukushima, Takehiko

    2012-01-01

    The concentration of polycyclic aromatic hydrocarbons (PAHs) and the toxicity to marine bacteria (Vibrio fischeri) were measured for the organic solvent extracts of sea sediments collected from an urban watershed area (Hiroshima Bay) of Japan and compared with the concentrations and toxicity of atmospheric particulate matter (PM). In atmospheric PM, the PAHs concentration was highest in fine particulate matter (FPM) collected during cold seasons. The concentrations of sea sediments were 0.01-0.001 times those of atmospheric PM. 1/EC50 was 1-10 L g(-1) PM for atmospheric PM and 0.1-1 L g(-1) dry solids for sea sediments. These results imply that toxic substances from atmospheric PM are diluted several tens or hundreds of times in sea sediments. The ratio of the 1/EC50 to PAHs concentration ((1/EC50)/16PAHs) was stable for all sea sediments (0.1-1 L μg(-1) 16PAHs) and was the same order of magnitude as that of FPM and coarse particulate matter (CPM). The ratio of sediments collected from the west was more similar to that of CPM while that from the east was more similar to FPM, possibly because of hydraulic differences among water bodies. The PAHs concentration pattern analyses (principal component analysis and isomer ratio analysis) were conducted and the results showed that the PAHs pattern in sea sediments was quite different to that of FPM and CPM. Comparison with previously conducted PAHs analyses suggested that biomass burning residues comprised a major portion of these other sources. PMID:22797225

  20. The investigation of atmospheric particulate matter pollution in Suzhou

    International Nuclear Information System (INIS)

    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, 20th 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

  1. Ultra fined-grained atmospheric particulate studied by magnetic analysis

    Science.gov (United States)

    Saragnese, F.; Lanci, L.; Lanza, R.

    2009-04-01

    We present the result of an investigation on the presence of ultrafine atmospheric particulate in the urban area of Turin by magnetic methods. Magnetic minerals are a common component of atmospheric particulate, mostly arising from a number of anthropogenic activities. Atmospheric particulate is well known to represent a serious health problem in urban area and recently the attention focused especially on fine (traffic area also support the previous finding that anthropogenic particulate has a large concentration of magnetic minerals compared to natural sources. Moreover the low temperature measurements have shown the presence of a relevant amount of ultrafine particles which are superparamagnetic at room temperature, their concentration increase in areas of high traffic and also appear to be related to anthropogenic sources. The magnetization carried by of ultrafine particles is site dependent but always larger than room temperature magnetization suggesting that about 60-70% of the particulate matter in urban area is made of ultrafine particles of nanometric size (< 30 nm). At given environmental conditions (site) the ratio between superparamagnetic and stable single domain magnetizations was found to remain fairly constant over time, thus allowing effortless predictions.

  2. SIMPLEX OPTIMIZATION OF MULTIELEMENT ULTRASONIC EXTRACTION OF ATMOSPHERIC PARTICULATES

    Science.gov (United States)

    A Simplex search was used to locate an optimum for an ultrasonic extraction of trace elements from atmospheric particulates collected on glass fiber high-volume sampler filters. The optimized procedure produced quantitative results for 13 elements with precisions of 10% or less, ...

  3. Occurrence and sources of particulate nitro-polycyclic aromatic hydrocarbons in ambient air in Denmark

    DEFF Research Database (Denmark)

    Feilberg, A.; Poulsen, M.W.B.; Nielsen, T.; Skov, H.

    2001-01-01

    been developed and applied. The nitro-PAK levels have been compared with levels of other air pollutants including unsubstituted PAHs, inorganic gases and particulate matter, as well as with meteorological parameters. Correlations and concentration ratios suggest that the dominant source of 9......-nitroanthracene at the urban site is direct emissions, whereas at the semirural site its dominant source is atmospheric formation. The atmospheric formation of 2-nitrofluoranthene and 2-nitropyrene generally seems to be initiated by OH radicals during the day rather than by NO3 radicals at night. The average...... contribution of the OH initiated formation is estimated to be in the range of 90-100%. However, under wintertime conditions with cloudy weather implying low OH radical production, NO3 radicals may also be important as initiators of nitro-PAH formation. Samples influenced by transport of polluted air masses...

  4. 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 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) concentration provide a better estimation of carcinogenicity activities; health risk to adults and children associated with PAHs inhalation was assessed by taking into account the lifetime average daily dose and corresponding incremental lifetime cancer risk (ILCR). The ILCR was within the acceptable range (10-6-10-4), indicating a low health risk to residents in these areas.

  5. Bioavailability and potential carcinogenicity of polycyclic aromatic hydrocarbons from wood combustion particulate matter in vitro.

    Science.gov (United States)

    Gauggel-Lewandowski, Susanne; Heussner, Alexandra H; Steinberg, Pablo; Pieterse, Bart; van der Burg, Bart; Dietrich, Daniel R

    2013-11-25

    Due to increasing energy demand and limited fossil fuels, renewable energy sources have gained in importance. Particulate matter (PM) in general, but also PM from the combustion of wood is known to exert adverse health effects in human. These are often related to specific toxic compounds adsorbed to the PM surface, such as polycyclic aromatic hydrocarbons (PAH), of which some are known human carcinogens. This study focused on the bioavailability of PAHs and on the tumor initiation potential of wood combustion PM, using the PAH CALUX® reporter gene assay and the BALB/c 3T3 cell transformation assay, respectively. For this, both cell assays were exposed to PM and their respective organic extracts from varying degrees of combustion. The PAH CALUX® experiments demonstrated a concentration-response relationship matching the PAHs detected in the samples. Contrary to expectations, PM samples from complete (CC) and incomplete combustion (IC) provided for a stronger and weaker response, respectively, suggesting that PAH were more readily bioavailable in PM from CC. These findings were corroborated via PAH spiking experiments indicating that IC PM contains organic components that strongly adsorb PAH thereby reducing their bioavailability. The results obtained with organic extracts in the cell transformation assay presented the highest potential for carcinogenicity in samples with high PAH contents, albeit PM from CC also demonstrated a carcinogenic potential. In conclusion, the in vitro assays employed emphasize that CC produces PM with low PAH content however with a general higher bioavailability and thus with a nearly similar carcinogenic potential than IC PM. PMID:23796820

  6. Analysis of Parent/Nitrated Polycyclic Aromatic Hydrocarbons in Particulate Matter 2.5 Based on Femtosecond Ionization Mass Spectrometry

    Science.gov (United States)

    Itouyama, Noboru; Matsui, Taiki; Yamamoto, Shigekazu; Imasaka, Tomoko; Imasaka, Totaro

    2016-02-01

    Particulate matter 2.5 (PM2.5), collected from ambient air in Fukuoka City, was analyzed by gas chromatography combined with multiphoton ionization mass spectrometry using an ultraviolet femtosecond laser (267 nm) as the ionization source. Numerous parent polycyclic aromatic hydrocarbons (PPAHs) were observed in a sample extracted from PM2.5, and their concentrations were determined to be in the range from 30 to 190 pg/m3 for heavy PPAHs. Standard samples of nitrated polycyclic aromatic hydrocarbons (NPAHs) were examined, and the limits of detection were determined to be in the picogram range. The concentration of NPAH adsorbed on PM2.5 in the air was less than 900-1300 pg/m3.

  7. Analysis of Parent/Nitrated Polycyclic Aromatic Hydrocarbons in Particulate Matter 2.5 Based on Femtosecond Ionization Mass Spectrometry.

    Science.gov (United States)

    Itouyama, Noboru; Matsui, Taiki; Yamamoto, Shigekazu; Imasaka, Tomoko; Imasaka, Totaro

    2016-02-01

    Particulate matter 2.5 (PM2.5), collected from ambient air in Fukuoka City, was analyzed by gas chromatography combined with multiphoton ionization mass spectrometry using an ultraviolet femtosecond laser (267 nm) as the ionization source. Numerous parent polycyclic aromatic hydrocarbons (PPAHs) were observed in a sample extracted from PM2.5, and their concentrations were determined to be in the range from 30 to 190 pg/m(3) for heavy PPAHs. Standard samples of nitrated polycyclic aromatic hydrocarbons (NPAHs) were examined, and the limits of detection were determined to be in the picogram range. The concentration of NPAH adsorbed on PM2.5 in the air was less than 900-1300 pg/m(3). Graphical Abstract ᅟ. PMID:26419772

  8. Polycyclic aromatic hydrocarbons in the airborne particulate matter at a location 40 km north of Bangkok, Thailand

    Science.gov (United States)

    Kim Oanh, N. T.; Bætz Reutergårdh, L.; Dung, N. Tr.; Yu, M.-H.; Yao, W.-X.; Co, H. X.

    Total suspended particulate matter in ambient air was sampled by high-volume samplers at four sites at the Asian Institute of Technology campus, west of the Phahonyothin Road, Phathumthani Province, 40 km North of Bangkok, Thailand. The concentrations of 18 polycyclic aromatic hydrocarbons (PAH), were measured by gas chromatography with flame ionisation and/or liquid chromatography with fluorescence detection. The PAH profile with relatively high concentrations of benzo(ghi)perylene and coronene, decreasing with the distance from the road, suggested a substantial contribution from the traffic. The concentrations in the core of the campus were in the same range as those reported for residential areas in the Bangkok Metropolitan.

  9. Mineralogy and geochemistry of atmospheric particulates in western Iran

    Science.gov (United States)

    Ahmady-Birgani, Hesam; Mirnejad, Hassan; Feiznia, Sadat; McQueen, Ken G.

    2015-10-01

    This study investigates the mineralogy and physico-chemical properties of atmospheric particulates collected at Abadan (southwestern Iran) near the Persian Gulf coast and Urmia (northwestern Iran) during ambient and dust events over 6 months (winter 2011; spring 2012). Particle sizes collected were: TSP (total suspended particulates); PM10 (particulates calcareous soils of the region. SEM observations indicated a wide range of particle morphologies over the 1-50 μm size range, with spherical, platy, cubic, elongate and prismatic shapes and rounding from angular to rounded. Energy dispersive X-ray analysis of TSP samples from both sites for non-dusty periods indicated that the sampled mineral suite contained Al, Mg, Na, Cl, P, S, Ca, K, Fe, Ti, and Si, mostly reflecting calcite, quartz, aluminosilicates, clays, gypsum and halite. Additionally, As, Pb, Zn, Mn, Sc, Nd, W, Ce, La, Ba and Ni were detected in TSP, PM10 and PM2.5 samples collected during dust events.

  10. Determination of oxygenated and native polycyclic aromatic hydrocarbons in urban dust and diesel particulate matter standard reference materials using pressurized liquid extraction and LC–GC/MS

    OpenAIRE

    Ahmed, Trifa M.; Bergvall, Christoffer; Åberg, Magnus; Westerholm, Roger

    2014-01-01

    The objective of this study was to develop a novel analytical chemistry method, comprised of a coupled high-performance liquid chromatography–gas chromatography/mass spectrometry system (LC–GC/MS) with low detection limits and high selectivity, for the identification and determination of oxygenated polycyclic aromatic hydrocarbons (OPAHs) and polycyclic aromatic hydrocarbons (PAHs) in urban air and diesel particulate matter. The linear range of the four OPAHs, which include 9,10-anthraquinone...

  11. Spatial correlativity of atmospheric particulate components simultaneously collected in Japan.

    Science.gov (United States)

    Funasaka, Kunihiro; Asakawa, Daichi; Oku, Yuichiro; Kishikawa, Naoya; Deguchi, Yuya; Sera, Nobuyuki; Seiyama, Tetsurou; Horasaki, Kazunori; Arashidani, Keiichi; Toriba, Akira; Hayakawa, Kazuichi; Watanabe, Masanari; Kataoka, Hiroyuki; Yamaguchi, Takako; Ikemori, Fumikazu; Inaba, Yohei; Tonokura, Kenichi; Akiyama, Masayuki; Kokunai, Osamu; Coulibaly, Souleymane; Hasei, Tomohiro; Watanabe, Tetsushi

    2016-02-01

    The simultaneous sampling of total suspended particles was performed at 14 sites in Japan during July 2008-June 2009. The spatial correlativity of each particulate composition toward Osaka was obtained for nine selected sites to overview the chemical composition and geographical distribution of particulate components across a wide range of areas nationwide. The spatial correlatives of atmospheric particulate components were extended to an even wider range of areas up to 950 km distance (meso-alpha scale region, >200 km) for a far-reaching distance analysis unique in the literature. Overall, the spatial correlations of ionic species and both organic and elemental carbons were significant, suggesting their shared advections, including their long-range transport from East Asia. Although sulfate ions are widely dispersed across Japan, such is not necessarily correlated with organic and elemental carbon, possibly indicating that the sulfate emission source, including long-range transport, differs from that of carbonaceous particulates. By contrast, the characteristics of spatial correlatives of metallic constituents vary; for example, particulate Pb and Cd show a significantly wide range of spatial correlatives to Osaka, while Mn-though limited to cities neighboring Osaka-shows significant spatial correlations. Other metallic constituents showed no significant spatial correlatives, indicating the effects of local pollutants. Moreover, the extent of the spatial dispersion of the particulate components and the relationships among chemical components were analyzed via factor analysis to highlight the effects of long-range inflow and local original emissions. In this treatment, 13 particulate components among the 19 measured were implicated in long-range transport. PMID:26753629

  12. Atmospheric chemistry of polycyclic aromatic compounds with special emphasis on nitro derivatives

    Energy Technology Data Exchange (ETDEWEB)

    Feilberg, A.

    2000-04-01

    Field measurements of polycyclic aromatic compounds (PAC) have been carried out at a semi-rural site and at an urban site. Correlation analyses, PAC indicators, and PAC ratios have been used to evaluate the importance of various sources of nitro-PAHs. A major source of nitro-PAHs is atmospheric transformation of PAHs initiated by OH radicals. Especially during long-range transport (LRT) of air pollution from Central Europe, the nitro-PAH composition in Denmark is dominated by nitro-PAHs formed in the atmosphere. Locally emitted nitro-PAHs are primarily from diesel vehicles. Levels of unsubstituted PAHs can also be strongly elevated in connection with LRT episodes. The ratio of 2-nitrofluoranthene relative to 1-nitropyrene is proposed as a measure of the relative photochemical age of particulate matter. Using this ratio, the relative mutagenicity of particle extracts appears to increase with increasing photochemical age. In connection with the field measurements, a method for measuring nitro-PAHs in particle extracts based on MS-MS detection has been developed. The atmospheric chemistry of nitronaphthalenes has been investigated with a smog chamber system combined with simulation with photochemical kinetics software. A methodology to implement gas-particle partitioning in a model based on chemical kinetics is described. Equilibrium constants (KP) for gas-particle partitioning of 1- and 2-nitronaphthalene have been determined. Mass transfer between the two phases appears to occur on a very short timescale. The gas phase photolysis of the nitronaphthalenes depends upon the molecular conformation. Significantly faster photolysis of 1-nitronaphthalene than of 2-nitronaphthalene is observed. The photochemistry of nitro-PAHs, and to some extent other PAC, associated with organic aerosols, has been studied with model systems simulating organic aerosol material. A number of aerosol constituents, including substituted phenols, benzaldehydes, and oxy-PAHs, are demonstrated to

  13. Quality control technique for high-volume atmospheric particulate sampler

    International Nuclear Information System (INIS)

    Quality control technique was developed for high-volume atmospheric particulate sampler. The flow meter of PMS-800 sampler was calibrated by an ISA1932 nozzle flow meter, and the global collection efficiency of PMS-800 sampler was tested by a type 2031 mobile sampler. The results show that the flowrate relative deviation between ISA1932 nozzle flow meter and PMS-800 sampler flow meter is less than 5%., and the global collection efficiency relative deviation between type 2031 sampler and PMS-800 sampler is less than 10%. The performance of PMS-800 sampler meets the specifications with the request of the Comprehensive Nuclear-Test-Ban Treaty. This method can be applied to quality control for high-volume atmospheric particulate sampler. (authors)

  14. Assessment of atmospheric distribution of polychlorinated biphenyls and polycyclic aromatic hydrocarbons using polyparameter model

    Directory of Open Access Journals (Sweden)

    Turk-Sekulić Maja M.

    2011-01-01

    Full Text Available Results of partial or total destruction of industrial plants, military targets, infrastructure, uncontrolled fires and explosions during the conflict period from 1991 to 1999, at the area of Western Balkans, were large amounts of hazardous organic matter that have been generated and emitted in the environment. In order to assess gas/particle partition of seven EPA polychlorinated biphenyls and sixteen EPA polycyclic aromatic hydrocarbons, twenty air samples have been collected at six urban, industrial and highly contaminated localities in Vojvodina. Hi-Vol methodology has been used for collecting ambiental air samples, that simultaneously collects gaseous and particulate phase with polyurethane foam filters (PUF and glass fiber filters (GFF. PUF and GFF filters have been analyzed, and concentration levels of gaseous PCBs and PAHs molecules in gaseous and particulate phase were obtained, converted and expressed through fraction of individual compounds sorbed onto particulate phase of the sample, in total detected quantity. Experimentally gained gas/particle partitioning values of PCBs and PAHs molecules have been compared with PP-LFER model estimated values. Significant deviation has been noticed during comparative analysis of estimated polyparameter model values for complete set of seven PCBs congeners. Much better agreement of experimental and estimated values is for polycyclic aromatic hydrocarbons, especially for molecules with four rings. These results are in a good correlation with literature data where polyparameter model has been used for predicting gas/particle partition of studied group of organic molecules.

  15. Atmospheric behaviors of polycyclic aromatic hydrocarbons at a Japanese remote background site, Noto peninsula, from 2004 to 2014

    Science.gov (United States)

    Tang, Ning; Hakamata, Mariko; Sato, Kousuke; Okada, Yumi; Yang, Xiaoyang; Tatematsu, Michiya; Toriba, Akira; Kameda, Takayuki; Hayakawa, Kazuichi

    2015-11-01

    Total suspended particulates were collected at a Japanese remote background site (Noto Air Monitoring Station; NAMS) on the Noto Peninsula from September 2004 to June 2014. Nine polycyclic aromatic hydrocarbons (PAHs) in the particulates (fluoranthene, pyrene, benz[a]anthracene, chrysene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, benzo[ghi]perylene and indeno[1,2,3-cd]pyrene) were determined by HPLC with fluorescence detection. The mean total concentrations of the nine PAHs in the cold season (November to May for the years 2004-2014) was 670 pg m-3 (range 37-4100 pg m-3). The mean total concentration in the warm season (June to October for the same period) was 170 pg m-3 (range 31-960 pg m-3). The atmospheric PAH level at NAMS decreased in recent years, although no significant change was found in the warm season. An analysis of meteorological conditions showed that the atmospheric PAHs at NAMS were long range transported from Northeast China in the cold seasons and were contributed to by Japanese domestic sources in the warm seasons. Lower concentration ratios of reactive PAHs to their isomers at NAMS also supported these results. Activities associated with the Beijing Olympic and Paralympic Games in 2008 and reconstruction after the 2007 Noto Hanto earthquake may have contributed to the yearly variations of atmospheric PAH levels at NAMS during the period 2007-2009. Source control measures implemented by the Chinese and Japanese governments appear to have been effective in decreasing the atmospheric PAH levels at NAMS in recent years.

  16. Spatial statistics of atmospheric particulate matter in China

    Science.gov (United States)

    Gao, Shenghui; Wang, Yangjun; Huang, Yongxiang; Zhou, Quan; Lu, Zhiming; Shi, Xiang; Liu, Yulu

    2016-06-01

    In this paper, the spatial dynamics of the atmospheric particulate matters (resp. PM10 and PM2.5) are studied using turbulence methodologies. It is found experimentally that the spatial correlation function ρ(r) shows a log-law on the mesoscale range, i.e., 50 ≤ r ≤ 500 km, with an experimental scaling exponent β = 0.45. The spatial structure function shows a power-law behavior on the mesoscale range 90 ≤ r ≤ 500 km. The experimental scaling exponent ζ(q) is convex, showing that the intermittent correction is relevant in characterizing the spatial dynamic of particulate matter. The measured singularity spectrum f(α) also shows its multifractal nature. Experimentally, the particulate matter is more intermittent than the passive scalar, which could be partially due to the mesoscale movements of the atmosphere, and also due to local sources, such as local industry activities.

  17. Investigation of sources of atmospheric polycyclic aromatic hydrocarbons at Mount Lushan in southern China

    Science.gov (United States)

    Li, Haiyan; Wang, Yan; Li, Hongli; Zhu, Chen; Mao, Huiting; Yang, Minmin; Wang, Ruixia; Wang, Wenxing

    2016-03-01

    Gaseous and particulate samples of polycyclic aromatic hydrocarbons (PAHs) were collected at the summit of Mount Lushan (29.58°N, 115.98°E, 1165 m asl) in southern China from August to September of 2011 and March to May of 2012 except special meteorological conditions such as rainy or very foggy days. The concentration of PAHs in total (gaseous and particulate PAHs) ranged from 15.79 to 160.53 ng m-3 (mean 41.67 ng m-3). Observed logarithmic values of particulate mass fraction (log θ) and partitioning coefficient (log Kp) were all higher than values calculated by the three gas-particle partitioning models, presenting higher fraction of particulate PAHs, indicating continual contribution of gaseous PAHs to particulate PAHs concentrations during long-range transport of air masses. Identified potential source regions using potential source contribution function analysis suggested significant contributions of emissions from coking, thermal power, and steel plants. The sources of PAHs levels at Mount Lushan that were identified using positive matrix factorization included diesel vehicles (43%), coal-fired boiler combustion (33%), coke oven source (17%), and incineration source (7%).

  18. Environmental atmosphere suspended particulate matter analysis using PIXE

    International Nuclear Information System (INIS)

    One of the environmental indicators of the atmosphere environment is suspended particulate matter (SPM). Recently, the concentration of particulate matter under 2.5 micro-meters (PM2.5) among SPM is regarded as important, and an environmental standard has been established for PM2.5 concentration. S.H.I. Examination and Inspection (SEI), Ltd. analyzes the components of PM2.5 by particle-induced X-ray emission (PIXE) using a Van de Graaff accelerator. SEI's PIXE analysis system quantifies the components by an external standard method. As a method for validating the reliability, the certified values of standard matter SRM2783 were compared with SEI's analysis values, and it was confirmed that the uncertainty of the analysis values of PM2.5 with this analysis system was within 10%. (author)

  19. Analysis of diesel particulate: influence of air-fuel ratio and fuel composition on polycyclic aromatic hydrocarbon content

    Energy Technology Data Exchange (ETDEWEB)

    Lombaert, K.; le Moyne, L.; Maleissye, Tardieu de [Universite Pierre et Marie Curie, Lab. de Mecanique Physique, Saint Cyr l' Ecole (France); Amouroux, J. [Ecole Nationale Superieure de Chimie, Lab. de Genie des Procedes Plasmas, Paris (France)

    2002-06-01

    Polycyclic aromatic hydrocarbons (PAH) are pollutants produced during the combustion process and are considered as soot precursors. PAH emissions are not presently regulated although they may have dangerous effects on human health. A comparison is presented here of the influence of engine parameters (air-fuel ratio and brake mean effective pressure) on the composition of particulates. The effects of a water-fuel emulsion on PAH (commonly examined in large engines) are also studied in a 1.9 L commonrail diesel engine: 13 per cent of water added to the fuel decreases the PAH concentration in diesel soot by half. The PAH emissions during cold-start of an automotive diesel engine are also presented. (Author)

  20. Chemical characterization and stable carbon isotopic composition of particulate polycyclic aromatic hydrocarbons issued from combustion of 10 Mediterranean woods

    Directory of Open Access Journals (Sweden)

    A. Guillon

    2012-08-01

    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 coupled with a mass spectrometer (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 different 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 from others origins of particulate matter (vehicular exhaust using isotopic measurements (with δ13CPAH = −28.7 to −26.6‰ 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 of source tracking.

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

    Directory of Open Access Journals (Sweden)

    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.

  2. Oxidative damage by carcinogenic polycyclic aromatic hydrocarbons and organic extracts from urban air particulate matter

    Czech Academy of Sciences Publication Activity Database

    Hanzalová, Kateřina; Rössner ml., Pavel; Šrám, Radim

    2010-01-01

    Roč. 696, č. 2 (2010), s. 114-121. ISSN 1383-5718 R&D Projects: GA MŠk 2B08005; GA MŽP(CZ) SP/1B3/8/08 Institutional research plan: CEZ:AV0Z50390512 Keywords : carcinogenic polycyclic aromatic hydrocarbons * oxidative damage in vitro * extractable organic matter Subject RIV: DN - Health Impact of the Environment Quality Impact factor: 2.938, year: 2010

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

    International Nuclear Information System (INIS)

    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

  4. Determination of oxygen and nitrogen derivatives of polycyclic aromatic hydrocarbons in fractions of asphalt mixtures using liquid chromatography coupled to mass spectrometry with atmospheric pressure chemical ionization.

    Science.gov (United States)

    Nascimento, Paulo Cicero; Gobo, Luciana Assis; Bohrer, Denise; Carvalho, Leandro Machado; Cravo, Margareth Coutinho; Leite, Leni Figueiredo Mathias

    2015-12-01

    Liquid chromatography coupled to mass spectrometry with atmospheric pressure chemical ionization was used for the determination of polycyclic aromatic hydrocarbon derivatives, the oxygenated polycyclic aromatic hydrocarbons and nitrated polycyclic aromatic hydrocarbons, formed in asphalt fractions. Two different methods have been developed for the determination of five oxygenated and seven nitrated polycyclic aromatic hydrocarbons that are characterized by having two or more condensed aromatic rings and present mutagenic and carcinogenic properties. The parameters of the atmospheric pressure chemical ionization interface were optimized to obtain the highest possible sensitivity for all compounds. The detection limits of the methods ranged from 0.1 to 57.3 μg/L for nitrated and from 0.1 to 6.6 μg/L for oxygenated derivatives. The limits of quantification were in the range of 4.6-191 μg/L for nitrated and 0.3-8.9 μg/L for oxygenated derivatives. The methods were validated against a diesel particulate extract standard reference material (National Institute of Standards and Technology SRM 1975), and the obtained concentrations (two nitrated derivatives) agreed with the certified values. The methods were applied in the analysis of asphalt samples after their fractionation into asphaltenes and maltenes, according to American Society for Testing and Material D4124, where the maltenic fraction was further separated into its basic, acidic, and neutral parts following the method of Green. Only two nitrated derivatives were found in the asphalt sample, quinoline and 2-nitrofluorene, with concentrations of 9.26 and 2146 mg/kg, respectively, whereas no oxygenated derivatives were detected. PMID:26446274

  5. Formation of Polycyclic Aromatic Hydrocarbons and Nitrogen Containing Polycyclic Aromatic Compounds in Titan's Atmosphere, the Interstellar Medium and Combustion

    Science.gov (United States)

    Landera, Alexander

    2013-12-01

    Several different mechanisms leading to the formation of (substituted) naphthalene and azanaphthalenes were examined using theoretical quantum chemical calculations. As a result, a series of novel synthetic routes to Polycyclic Aromatic Hydrocarbons (PAHs) and Nitrogen Containing Polycyclic Aromatic Compounds (N-PACs) have been proposed. On Earth, these aromatic compounds originate from incomplete combustion and are released into our environment, where they are known to be major pollutants, often with carcinogenic properties. In the atmosphere of a Saturn's moon Titan, these PAH and N-PACs are believed to play a critical role in organic haze formation, as well as acting as chemical precursors to biologically relevant molecules. The theoretical calculations were performed by employing the ab initio G3(MP2,CC)/B3LYP/6-311G** method to effectively probe the Potential Energy Surfaces (PES) relevant to the PAH and N-PAC formation. Following the construction of the PES, Rice-Ramsperger-Kassel-Markus (RRKM) theory was used to evaluate all unimolecular rate constants as a function of collision energy under single-collision conditions. Branching ratios were then evaluated by solving phenomenological rate expressions for the various product concentrations. The most viable pathways to PAH and N-PAC formation were found to be those where the initial attack by the ethynyl (C2H) or cyano (CN) radical toward a unsaturated hydrocarbon molecule led to the formation of an intermediate which could not effectively lose a hydrogen atom. It is not until ring cyclization has occurred, that hydrogen elimination leads to a closed shell product. By quenching the possibility of the initial hydrogen atom elimination, one of the most competitive processes preventing the PAH or N-PAC formation was avoided, and the PAH or N-PAC formation was allowed to proceed. It is concluded that these considerations should be taken into account when attempting to explore any other potential routes towards

  6. Exposure to daily ambient particulate polycyclic aromatic hydrocarbons and cough occurrence in adult chronic cough patients: A longitudinal study

    Science.gov (United States)

    Anyenda, Enoch Olando; Higashi, Tomomi; Kambayashi, Yasuhiro; Thao, Nguyen Thi Thu; Michigami, Yoshimasa; Fujimura, Masaki; Hara, Johsuke; Tsujiguchi, Hiromasa; Kitaoka, Masami; Asakura, Hiroki; Hori, Daisuke; Yamada, Yohei; Hayashi, Koichiro; Hayakawa, Kazuichi; Nakamura, Hiroyuki

    2016-09-01

    The specific components of airborne particulates responsible for adverse health effects have not been conclusively identified. We conducted a longitudinal study on 88 adult patients with chronic cough to evaluate whether exposure to daily ambient levels of particulate polycyclic aromatic hydrocarbons (PAH) has relationship with cough occurrence. Study participants were recruited at Kanazawa University Hospital, Japan and were physician-diagnosed to at least have asthma, cough variant asthma and/or atopic cough during 4th January to 30th June 2011. Daily cough symptoms were collected by use of cough diaries and simultaneously, particulate PAH content in daily total suspended particles collected on glass fiber filters were determined by high performance liquid chromatography coupled with fluorescence detector. Population averaged estimates of association between PAH exposure and cough occurrence for entire patients and subgroups according to doctor's diagnosis were performed using generalized estimating equations. Selected adjusted odds ratios for cough occurrence were 1.088 (95% confidence interval (CI): 1.031, 1.147); 1.209 (95% CI: 1.060, 1.379) per 1 ng/m3 increase for 2-day lag and 6-day moving average PAH exposure respectively. Likewise, 5 ring PAH had higher odds in comparison to 4 ring PAH. On the basis of doctor's diagnosis, non-asthma group had slightly higher odds ratio 1.127 (95% CI: 1.033, 1.228) per 1 ng/m3 increase in 2-day lag PAH exposure. Our findings suggest that ambient PAH exposure is associated with cough occurrence in adult chronic cough patients. The association may be stronger in non-asthma patients and even at low levels although there is need for further study with a larger sample size of respective diagnosis and inclusion of co-pollutants.

  7. Toxicity assessment of atmospheric particulate matter in the Mediterranean and Black Seas open waters.

    Science.gov (United States)

    Mesquita, Sofia R; Dachs, Jordi; van Drooge, Barend L; Castro-Jiménez, Javier; Navarro-Martín, Laia; Barata, Carlos; Vieira, Natividade; Guimarães, Laura; Piña, Benjamin

    2016-03-01

    Atmospheric deposition of particulate matter (PM) is recognized as a relevant input vector for toxic compounds, such as polycyclic aromatic hydrocarbons (PAHs), into the marine environment. In this work we aimed to analyse the biological activity and potential adverse effects of PM constituents to aquatic organisms. Organic extracts of atmospheric PM samples from different sub-basins of the Mediterranean and Black Seas were screened using different toxicological tests. A yeast-based assay (AhR-RYA) revealed that dioxin-like activity correlated with the concentration of total PAHs in the PM samples, as well as with their predicted toxic equivalent values (TEQs). Although the zebrafish embryotoxicity test (the ZET assay) showed no major phenotypical adverse effects, up-regulation of mRNA expression of cyp1a, fos and development-related genes (previously described as related to PM toxicity) was observed in exposed embryos when compared to controls. Results showed that mRNA patterns of the studied genes followed a similar geographic distribution to both PAH content and dioxin-like activity of the corresponding extracts. The analysis also showed a distinct geographical pattern of activation of pancreatic markers previously related to airborne pollution, probably indicating a different subset of uncharacterized particle-bound toxicants. We propose the combination of the bioassays tested in the present study to be applied to future research with autochthonous species to assess exposure and potential toxic effects of ambient PM. The present study emphasizes the need for more in-depth studies into the toxic burden of atmospheric PM on aquatic ecosystems, in order to improve future regulatory guidelines. PMID:26745302

  8. Salmonella mutagenicity assessment of airborne particulate matter collected from urban areas of Rio Grande do Sul State, Brazil, differing in anthropogenic influences and polycyclic aromatic hydrocarbon levels.

    Science.gov (United States)

    Pereira, Tatiana S; Gotor, Gemma N; Beltrami, Laiana S; Nolla, Celia G; Rocha, Jocelita A V; Broto, Francesc P; Comellas, Lluis R; Vargas, Vera M F

    2010-09-30

    Urban areas are both major sources and major targets of air pollution. The atmospheric environment receives diverse chemical substances, including genotoxic agents that may affect human health. The purpose of this study was to evaluate and compare the atmospheric quality in two urban areas in Rio Grande do Sul State (Brazil), under the influence of greater (Site 1) or lesser (Site 2) anthropogenic sources. Polycyclic aromatic hydrocarbons (PAHs) of environmental interest were quantified and the Salmonella/microsome assay was used for the measurement of mutagenicity. Organic compounds extracted from the airborne particulate matter were analyzed by high-performance liquid chromatography (HPLC) to detect PAHs of interest (known or possible carcinogens). The organic extracts were also tested for mutagenic and cytotoxic activity in the Salmonella/microsome assay with strains TA98, TA100, YG1021 and YG1024, with or without S9 activation. At Site 1, benzo[ghi]perylene (BghiP) and indeno[1,2,3-cd]pyrene (IP) were found at higher concentrations and mutagenicity (revertants per μg extract) varied from 1.0±0.25 (TA98, no S9) to 5.2±0.45 (TA98, S9). At Site 2, BghiP and IP were present in larger amounts and the mutagenic responses ranged from 0.6 to 3.7 revertants per μg (both in TA98, S9). The occurrence of BghiP and IP may be related to vehicular emissions. These and the other PAHs studied, as well as the nitro compounds, may contribute to the mutagenicity found in these airborne particles. PMID:20643224

  9. Free amino acids in atmospheric particulate matter of Venice, Italy

    Science.gov (United States)

    Barbaro, Elena; Zangrando, Roberta; Moret, Ivo; Barbante, Carlo; Cescon, Paolo; Gambaro, Andrea

    2011-09-01

    The concentrations of free amino acids were determined in atmospheric particulate matter from the city of Venice (Italy) in order to better understand their origin. The analysis of aerosol samples was carried out via high-performance liquid chromatography coupled to a triple quadrupole tandem mass spectrometric detector (HPLC/ESI-MS/MS). The internal standard method was used and the analytical procedure was validated by evaluating the trueness, the precision, the recovery, the detection and the quantification limits. The particulate matter was collected using quartz fiber filters and extracted in methanol; after filtration the extract was directly analyzed. Forty samples were collected from April to October 2007 and the average concentrations of free amino acids in the aerosol were: alanine 35.6 pmol m -3, aspartic acid 31.1 pmol m -3, glycine 30.1 pmol m -3, glutamic acid 32.5 pmol m -3, isoleucine 2.4 pmol m -3, leucine 2.7 pmol m -3, methionine, cystine and 3-hydroxy-proline below the limit of detection, phenylalanine 2.8 pmol m -3, proline 43.3 pmol m -3, serine 8.6 pmol m -3, threonine 2.8 pmol m -3, tyrosine 1.7 pmolm -3, valine 3.8 pmol m -3, asparagine 70.2 pmol m -3, glutamine 38.0 pmol m -3, 4-hydroxy-proline 2.5 pmol m -3, methionine sulfoxide 1.1 pmol m -3, and methionine sulfone 0.1 pmol m -3. The total average concentration of these free amino acids in aerosol samples of Venice Lagoon was 334 pmol m -3. The temporal evolution and multivariate analysis indicated the photochemical origin of 4-hydroxy-proline and methionine sulfoxide and for other compounds an origin further away from the site of sampling, presumably reflecting transport from terrestrial sources.

  10. Determination of polycyclic aromatic hydrocarbons in fractions in asphalt mixtures using liquid chromatography coupled to mass spectrometry with atmospheric pressure chemical ionization.

    Science.gov (United States)

    Nascimento, Paulo Cicero; Gobo, Luciana Assis; Bohrer, Denise; Carvalho, Leandro Machado; Cravo, Margareth Coutinho; Leite, Leni Figueiredo Mathias

    2015-07-01

    An analytical method using liquid chromatography coupled to mass spectrometry with atmospheric pressure chemical ionization for the determination of polycyclic aromatic hydrocarbons in asphalt fractions has been developed. The 14 compounds determined, characterized by having two or more condensed aromatic rings, are expected to be present in asphalt and are considered carcinogenic and mutagenic. The parameters of the atmospheric pressure chemical ionization interface were optimized to obtain the highest possible sensitivity for all of the compounds. The limits of detection ranged from 0.5 to 346.5 μg/L and the limits of quantification ranged from 1.7 to 1550 μg/L. The method was validated against a diesel particulate extract standard reference material (NIST SRM 1975), and the obtained concentrations agreed with the certified values. The method was applied to asphalt samples after its fractionation according to ASTM D4124 and the method of Green. The concentrations of the seven polycyclic aromatic hydrocarbons quantified in the sample ranged from 0.86 mg/kg for benzo[ghi]perylene to 98.32 mg/kg for fluorene. PMID:25885756

  11. Characterizing priority polycyclic aromatic hydrocarbons (PAH) in particulate matter from diesel and palm oil-based biodiesel B15 combustion

    Science.gov (United States)

    Rojas, Nestor Y.; Milquez, Harvey Andrés; Sarmiento, Hugo

    2011-11-01

    A set of 16 priority polycyclic aromatic hydrocarbons (PAH) associated with particulate matter (PM), emitted by a diesel engine fueled with petroleum diesel and a 15%-vol. palm oil methyl ester blend with diesel (B15), were determined. PM was filtered from a sample of the exhaust gas with the engine running at a steady speed and under no load. PAH were extracted from the filters using the Soxhlet technique, with dichloromethane as solvent. The extracts were then analyzed by gas chromatography using a flame ionization detector (FID). No significant difference was found between PM mass collected when fueled with diesel and B15. Ten of the 16 PAH concentrations were not reduced by adding biodiesel: Benz(a)anthracene, benzo(a)pyrene, benzo(b)fluoranthene, chrysene, dibenz(a,h)anthracene, fluoranthene, fluorene, indeno(1,2,3-c,d)pyrene, naphthalene and phenanthrene. The acenaphthene, acenaphthylene and anthracene concentrations were 45%-80% higher when using diesel, whereas those for benzo(k)fluoranthene, benzo(g,h,i)perylene and pyrene were 30%-72% higher when using the B15 blend. Even though the 16 priority-PAH cumulative concentration increased when using the B15 blend, the total toxic equivalent (TEQ) concentration was not different for both fuels.

  12. Polycyclic Aromatic Hydrocarbons and n-alkanes in Suspended Particulate Matter and Sediments from the Langat River, Peninsular Malaysia

    Directory of Open Access Journals (Sweden)

    Alireza Riyahi Bakhtiari

    2009-07-01

    Full Text Available The Langat River basin has seen rapid developments in industrialization, urbanization and dramatic population increases during the past two decades. The composition and sources of polycyclic aromatic hydrocarbons (PAHs and aliphatic hydrocarbon (n-alkanes concentrations were determined in surface sediments (SS and suspended particulate matter (SPM collected from six locations in the Langat River. The total n-alkanes concentrations (∑HC ranged from 5900 to 23000 µg/g in SPM and 1700 to 8600 µg/g in SS samples. Total PAHs concentrations varied from 306 to 7968 ng/g in SPM and 558 to 980 ng/g in SS. PAHs and n-alkanes were dominated by higher molecular weight compounds in SS and low-medium molecular weight compounds in SPM. Carbon preference index (CPI values for n-alkanes in ranges C 25-33, C 15-35 and C 25-35 varied from 0.95 to 2.49 in SS and close to unity in SPM. The CPIs values indicated multiple n-alkanes sources (petrogenic and natural. PAHs isomer pairs ratios indicated multiple (petrogenic and pyrogenic with predominance of pyrogenic PAH sources. Analysis of the possible source of PAHs and n-alkanes indicated a complicated, combined PAHs and n-alkanes source in the Langat River.

  13. Characterisation of particulates and carcinogenic polycyclic aromatic hydrocarbons in wintertime wood-fired heating in residential areas

    Science.gov (United States)

    Bari, Md. Aynul; Baumbach, Guenter; Brodbeck, Johannes; Struschka, Michael; Kuch, Bertram; Dreher, Werner; Scheffknecht, Guenter

    2011-12-01

    Wood as a renewable and worldwide available fuel is used for residential heating in small-scale firings during winter. This wood combustion can cause very high emissions of inhalable particles resulting in short and long-term health effects. The target of this study was to characterise particulate matter, emissions of polycyclic aromatic hydrocarbons (PAHs) and their size distribution and to show that those emissions can be found in the ambient air of residential areas with wood-fired heating. Emission samples were collected from pellet stove and log wood boiler under different combustion conditions. Ambient PM 10 sampling was performed during two winter seasons at two rural residential areas near Stuttgart in Germany. Samples were extracted using toluene with ultrasonic bath and analysed by gas chromatography mass spectrometry (GC-MS). Twenty-one PAH compounds including nine carcinogenic ones were detected and quantified. It was found that emission concentrations of carcinogenic PAHs were higher during incomplete combustion compared to complete combustion. Significant amounts of ambient PAHs were found in the residential villages, where the contribution of carcinogenic PAHs was 44% of total PAHs in the ambient air during winter 2009. The morphology and elemental analysis of ambient particles were also investigated. The findings indicate a rising concern to reduce emissions from wood-fired heating during winter in residential areas and underline the importance of using good wood combustion technologies to improve the air quality.

  14. Spatial and temporal distribution of polycyclic aromatic hydrocarbons (PAHs) in the atmosphere of Xiamen, China

    International Nuclear Information System (INIS)

    An intensive sampling program was conducted from October 2008 to September 2009 at the five different environmental sites in Xiamen, Fujian Province, to study the spatial and temporal characteristics of Polycyclic Aromatic Hydrocarbons (PAHs) in the gaseous and particulate phase, respectively. The PAHs concentrations at different sites were quite distinct during four seasons. The average concentrations of PAHs in winter were about 8.4 times higher than those in spring, and the concentrations of background were 0.56 times lower than those of industrial area. In addition, the higher temperature in summer affected the particle/gas partitioning of PAHs and led to the higher concentrations of gaseous PAHs. Diagnostic ratios of PAHs, which were employed to indicate the primary sources of PAHs in Xiamen, showed that the traffic vehicle exhaust was the largest contributor and the primary source for PAHs in Xiamen, especially in urban area; while the stationary combustion processes, such as petrochemical factories and power plants, were mainly responsible for PAHs sources in the industrial areas. The health risk of PAHs in the particulate phase was higher than those of the gaseous phase at the five sampling sites. The average toxic equivalent (BaPeq) of the benzo[a]pyrene values for PAHs were 0.14, 0.32, 1.38 and 3.59 ng m-3 in spring, summer, autumn and winter, respectively. Furthermore, the results of average BaPeq in all four seasons indicated that the health risks of particulate PAHs were higher than those of the gaseous PAHs at different sampling sites.

  15. Optimisation of supercritical fluid extraction of polycyclic aromatic hydrocarbons and their nitrated derivatives adsorbed on highly sorptive diesel particulate matter

    Energy Technology Data Exchange (ETDEWEB)

    Portet-Koltalo, F., E-mail: florence.koltalo@univ-rouen.fr [Laboratoire d' Analyse des Systemes Organiques Complexes, IRCOF et IFRMP, Universite de Rouen, 55 rue Saint Germain, 27000 Evreux (France); Oukebdane, K. [Laboratoire d' Analyse des Systemes Organiques Complexes, IRCOF et IFRMP, Universite de Rouen, 55 rue Saint Germain, 27000 Evreux (France); Dionnet, F. [CERTAM, Technopole du Madrillet, 1 rue Joseph Fourier, 76800 Saint Etienne du Rouvray (France); Desbene, P.L. [Laboratoire d' Analyse des Systemes Organiques Complexes, IRCOF et IFRMP, Universite de Rouen, 55 rue Saint Germain, 27000 Evreux (France)

    2009-09-28

    Supercritical fluid extraction (SFE) was performed to extract complex mixtures of polycyclic aromatic hydrocarbons (PAHs), nitrated derivatives (nitroPAHs) and heavy n-alkanes from spiked soot particulates that resulted from the incomplete combustion of diesel oils. This polluted material, resulting from combustion in a light diesel engine and collected at high temperature inside the particulate filter placed just after the engine, was particularly resistant to conventional extraction techniques, such as soxhlet extraction, and had an extraction behaviour that differed markedly from certified reference materials (SRM 1650). A factorial experimental design was performed, simultaneously modelling the influence of four SFE experimental factors on the recovery yields, i.e.: the temperature and the pressure of the supercritical fluid, the nature and the percentage of the organic modifier added to CO{sub 2} (chloroform, tetrahydrofuran, methylene chloride), as a means to reach the optimal extraction yields for all the studied target pollutants. The results of modelling showed that the supercritical fluid pressure had to be kept at its maximum level (30 MPa) and the temperature had to be kept relatively low (75 {sup o}C). Under these operating conditions, adding 15% of methylene chloride to the CO{sub 2} permitted quantitative extraction of not only light PAHs and their nitrated derivatives, but also heavy n-alkanes from the spiked soots. However, heavy polyaromatics were not quantitatively extracted from the refractory carbonaceous solid surface. As such, original organic modifiers were tested, including pyridine, which, as a strong electron donor cosolvent (15% into CO{sub 2}), was the most successful. The addition of diethylamine to pyridine, which enhanced the electron donor character of the cosolvent, even increased the extraction yields of the heaviest PAHs, leading to a quantitative extraction of all PAHs (more than 79%) from the diesel particulate matter, with

  16. Optimisation of supercritical fluid extraction of polycyclic aromatic hydrocarbons and their nitrated derivatives adsorbed on highly sorptive diesel particulate matter

    International Nuclear Information System (INIS)

    Supercritical fluid extraction (SFE) was performed to extract complex mixtures of polycyclic aromatic hydrocarbons (PAHs), nitrated derivatives (nitroPAHs) and heavy n-alkanes from spiked soot particulates that resulted from the incomplete combustion of diesel oils. This polluted material, resulting from combustion in a light diesel engine and collected at high temperature inside the particulate filter placed just after the engine, was particularly resistant to conventional extraction techniques, such as soxhlet extraction, and had an extraction behaviour that differed markedly from certified reference materials (SRM 1650). A factorial experimental design was performed, simultaneously modelling the influence of four SFE experimental factors on the recovery yields, i.e.: the temperature and the pressure of the supercritical fluid, the nature and the percentage of the organic modifier added to CO2 (chloroform, tetrahydrofuran, methylene chloride), as a means to reach the optimal extraction yields for all the studied target pollutants. The results of modelling showed that the supercritical fluid pressure had to be kept at its maximum level (30 MPa) and the temperature had to be kept relatively low (75 oC). Under these operating conditions, adding 15% of methylene chloride to the CO2 permitted quantitative extraction of not only light PAHs and their nitrated derivatives, but also heavy n-alkanes from the spiked soots. However, heavy polyaromatics were not quantitatively extracted from the refractory carbonaceous solid surface. As such, original organic modifiers were tested, including pyridine, which, as a strong electron donor cosolvent (15% into CO2), was the most successful. The addition of diethylamine to pyridine, which enhanced the electron donor character of the cosolvent, even increased the extraction yields of the heaviest PAHs, leading to a quantitative extraction of all PAHs (more than 79%) from the diesel particulate matter, with detection limits ranging

  17. KEY COMPARISON: CCQM-K50: Polycyclic aromatic hydrocarbons (PAHs) in soil/particulate matter

    Science.gov (United States)

    Philipp, R.; Bremser, W.; Becker, R.; Win, T.; Schantz, M. M.; Pérez Urquiza, M.; Ávila Calderón, M. A.; Maldonado Torres, M.; Carter, D.; O'Connor, G.; Sejeroe-Olsen, B.; Ricci, M.; Lalere, B.; Peignaux, M.; Kim, D. H.; Itoh, N.; Wong, S.; Man, T. O.; Marques Rodrigues Caixeiro, J.

    2010-01-01

    There are numerous Calibration and Measurement Capability Claims (CMCs) on PAH analysis in various matrices published in the BIPM key comparison database, Appendix C. By July 2007 such CMCs were released in Category 10 Biological fluids and materials, Subcategory 10.4 Tissues, Category 11 Food, Subcategory 11.2 Contaminants and Category 13 Sediments, soils, ores and particulates, Subcategories 13.1 Sediments, 13.2 Soils and 13.4 Particulates. CCQM comparisons are needed to underpin these claims. A pilot study CCQM-P69 'PAHs in soil' was successfully conducted in 2004. After review of the results at the OAWG meeting in September 2005 it was decided to proceed with a key comparison and a concurrent second pilot study CCQM-K50/P69.1. CENAM and BAM agreed to coordinate the intercomparison. The measurand of the study was specified as amount of specific PAHs in solid matrices as extracted under exhaustive extraction conditions. As for the preceding pilot study and two studies for PAHs in solution (CCQM-P31a and CCQM-K38), five target analytes, phenanthrene, fluoranthene, benz[a]anthracene, benzo[a]pyrene and benzo[ghi]perylene, were selected as representative of the measurement of individual compounds. The CCQM-K50 study utilized a soil sample from BAM and an air particulate sample from NIST. Both materials were naturally contaminated, not enriched or spiked. The mass fraction of target analytes in the samples ranged from 2 mg/kg to 15 mg/kg. NIST SRM 1649a Urban Dust was provided as a control material. Participants were requested to determine the mass fraction of the selected PAHs on a dry mass basis and submit a complete uncertainty budget for their measurements. Ten NMIs participated in the study. All participants applied Soxhlet or Accelerated Solvent extraction (ASE) and GC-MS with either deuterated or 13C labelled internal standards. Results demonstrate a good level of equivalence in capabilities of the participating NMIs to identify and measure PAHs in highly

  18. Investigations into a novel method for atmospheric polycyclic aromatic hydrocarbon monitoring

    International Nuclear Information System (INIS)

    A novel analytical method for atmospheric polycyclic aromatic hydrocarbons (PAHs) was developed based on laser induced fluorescence (LIF) of samples on quartz multi-channel polydimethylsiloxane traps. A tunable dye laser with a frequency doubling crystal provided the excitation radiation, and a double monochromator with a photomultiplier tube detected emitted fluorescence. The method allowed for the rapid (-3), as photodegradation was minimal (15 min irradiation, included phenol, benzyl alcohol and phthalic anhydride. Without any signal optimization, a LIF detection limit of ∼1 μg m-3 was established for naphthalene using a diffusion tube (diffusion rate of 2 ng s-1) and 292 nm excitation. - A novel method for rapid analysis of atmospheric PAHs by laser induced fluorescence allows for more detailed trend determinations.

  19. Contribution of biomass burning to atmospheric polycyclic aromatic hydrocarbons at three European background sites

    Energy Technology Data Exchange (ETDEWEB)

    Manolis Mandalakis; Oerjan Gustafsson; Tomas Alsberg; Anna-Lena Egebaeck; Christopher M. Reddy; Li Xu; Jana Klanova; Ivan Holoubek; Euripides G. Stephanou [Stockholm University, Stockholm (Sweden). Department of Applied Environmental Science (ITM)

    2005-05-01

    Radiocarbon analysis of atmospheric polycyclic aromatic hydrocarbons (PAHs) from three background areas in Sweden, Croatia, and Greece was performed to apportion their origin between fossil and biomass combustion. Diagnostic ratios of PAHs implied that wood and coal combustion was relatively more important in the northern European site, while combustion of fossil fuels was the dominant source of PAHs to the two central-southern European background sites. The radiocarbon content ({Delta}{sup 14}C) of atmospheric PAHs in Sweden ranged between -388{per_thousand} and -381{per_thousand}, while more depleted values were observed for Greece (-914{per_thousand}) and Croatia (-888{per_thousand}). Using a 14C isotopic mass balance model it was calculated that biomass burning contributes nearly 10% of the total PAH burden in the studied southern European atmosphere with fossil fuel combustion making up the 90% balance. In contrast, biomass burning contributes about 50% of total PAHs in the atmosphere at the Swedish site. Results suggest that the relative contributions of biomass burning and fossil fuels to atmospheric PAHs may differ considerably between countries, and therefore, different national control strategies might be needed if a further reduction of these pollutants is to be achieved on a continental-global scale. 54 refs., 2 figs., 1 tab.

  20. Source apportionment of atmospheric fine particulate matter collected at the Seney National Wildlife Refuge

    Data.gov (United States)

    US Fish and Wildlife Service, Department of the Interior — The trends in secondary organic aerosol at a remote location are studied using atmospheric fine particulate matter samples collected at Seney National Wildlife...

  1. Induction of c-Jun by air particulate matter (PM10) of Mexico city: Participation of polycyclic aromatic hydrocarbons

    International Nuclear Information System (INIS)

    The carcinogenic potential of urban particulate matter (PM) has been partly attributed to polycyclic aromatic hydrocarbons (PAHs) content, which activates the aryl hydrocarbon receptor (AhR). Here we report the effect of PM with an aerodynamic size of 10 μm (PM10) on the induction of AhR pathway in A549 cells, evaluating its downstream targets CYP1B1, IL-6, IL-8 and c-Jun. Significant increases in CYP1B1 protein and enzyme activity; IL-6 and IL-8 secretion and c-Jun protein were found in response to PM10. The formation of PAH-DNA adducts was also detected. The involvement of AhR pathway was confirmed with Resveratrol as AhR antagonist, which reversed CYP1B1 and c-Jun induction. Nevertheless, in IL-6 and IL-8 secretion, the Resveratrol was ineffective, suggesting an effect independent of this pathway. Considering the role of c-Jun in oncogenesis, its induction by PM may be contributing to its carcinogenic potential through induction of AhR pathway by PAHs present in PM10. - Highlights: • We analyzed the induction of AhR pathway targets by exposure to PM10 in A549 cells. • We suggest that PAHs content in PM10 are responsible for the induction of c-Jun. • C-Jun induction could represent part of mechanism of carcinogenicity of PM10. - We report the role of the aryl hydrocarbon receptor pathway in cJun induction caused by PM10 exposure in human lung cells, which could represent part of its mechanism of carcinogenicity

  2. Polycyclic aromatic hydrocarbons (PAHs in the atmospheres of two French alpine valleys: sources and temporal patterns

    Directory of Open Access Journals (Sweden)

    N. Marchand

    2004-01-01

    Full Text Available Alpine valleys represent some of the most important crossroads for international heavy-duty traffic in Europe, but the full impact of this traffic on air quality is not known due to a lack of data concerning these complex systems. As part of the program "Pollution des Vallées Alpines" (POVA, we performed two sampling surveys of polycyclic aromatic hydrocarbons (PAHs in two sensitive valleys: the Chamonix and Maurienne Valleys, between France and Italy. Sampling campaigns were performed during the summer of 2000 and the winter of 2001, with both periods taking place during the closure of the "Tunnel du Mont-Blanc". The first objective of this paper is to describe the relations between PAH concentrations, external parameters (sampling site localization, meteorological parameters, sources, and aerosol characteristics, including its carbonaceous fraction (OC and EC. The second objective is to study the capacity of PAH profiles to accurately distinguish the different emission sources. Temporal evolution of the relative concentration of an individual PAH (CHR and the PAH groups BghiP+COR and BbF+BkF is studied in order to differentiate wood combustion, gasoline, and diesel emissions, respectively. The results show that the total particulate PAH concentrations were higher in the Chamonix valley during both seasons, despite the cessation of international traffic. Seasonal cycles, with higher concentrations in winter, are also stronger in this valley. During winter, particulate PAH concentration can reach very high levels (up to 155 ng.m-3 in this valley during cold anticyclonic periods. The examination of sources shows the impact during summer of heavy-duty traffic in the Maurienne valley and of gasoline vehicles in the Chamonix valley. During winter, Chamonix is characterized by the strong influence of wood combustion in residential fireplaces, even if the temporal evolution of specific PAH ratios are difficult to interpret. Information on sources

  3. Pollution level, inhalation exposure and lung cancer risk of ambient atmospheric polycyclic aromatic hydrocarbons (PAHs) in Taiyuan, China

    International Nuclear Information System (INIS)

    Passive air samplers were deployed to collect both gas and particulate phase polycyclic aromatic hydrocarbons in Taiyuan between 2009 and 2010. Annual average concentrations of BaP equivalent concentration (B[a]Peq) in background, rural and urban areas were 2.90 ± 0.29, 23.2 ± 30.8 and 27.4 ± 28.1 ng/m3, respectively, with higher concentration in the winter than in other seasons. The median B[a]Peq concentrations of annual inhalation exposure were estimated to be in the range of 103–347 ng/d for all population groups in rural as well as in urban areas. The median values of incremental lifetime cancer risk (ILCR) induced by whole year inhalation exposure for all groups were basically larger than 10−6, with higher values in winter than in other seasons and in urban than in rural area. In the same season and area, the ILCR of adults was larger than other age groups and that of females was a little higher than males. - Highlights: ► The median values of ILCR were higher in winter than in other seasons. ► The median values of ILCR were higher in urban than in rural area. ► In the same season and area, the ILCR of adults was larger than other age groups. ► In the same season and area, the ILCR of females was a little higher than males. ► Exposure level and the cancer slope factor influenced the ILCR greatly. - The inhalation exposure and lung cancer risk of ambient atmospheric PAHs changed for different seasons, areas and population groups in Taiyuan, China.

  4. Characteristics of the aerosol particulates in the atmosphere in an urban environment at Faisalabad, Pakistan

    International Nuclear Information System (INIS)

    The deposition of trace and major elements from the atmosphere to the ground is an important factor for plants, animals and humans as well. Total suspended particulate matter was measured by a standard gravimetric technique. A scanning electron microscope was used for the evaluation of the size distribution and morphological structures of the aerosol particulates trapped on the surface of filter paper. The aerosol particulates were studied by a scanning electron microscope at various magnification. The trace elemental composition in the atmosphere of Faisalabad was studied by using instrumental neutron activation analysis (INAA) and atomic absorption spectrometry (AAS). Concentrations of 23 trace elements and a major one were determined in samples of aerosol particulates collected during a longe sampling period in the atmosphere at Faisalabad, Pakistan. Their amount was two times higher than the limits adopted by the U.S. Environmental Protection Agency for the urban environment. (author)

  5. Source identification of Malaysian atmosphere polycyclic aromatic hydrocarbons nearby forest fires using molecular and isotopic compositions

    Energy Technology Data Exchange (ETDEWEB)

    Okuda, Tomoaki; Takada, Hideshige [Tokyo Univ. of Agriculture and Technology (Japan). Faculty of Agriculture; Kumata, Hidetoshi [Tokyo Univ. of Pharmacy and Life Sciences (Japan); Zakaria, M.P. [Universiti Putra Malaysia, Selangor (Malaysia). Dept. of Environmental Sciences; Naraoka, Hiroshi; Ishiwatari, Ryoshi [Tokyo Metropolitan Univ., Hachioji (Japan). Graduate School of Science

    2002-07-01

    We report measurements of molecular and carbon isotopic compositions of Malaysian atmospheric polycyclic aromatic hydrocarbons (PAHs) in smoke haze from the 1997 Indonesian forest fire. Comparison of the carbon isotopic compositions ({sup {delta}}1{sup 3C}) of individual PAHs from the smoke haze, with those from other PAHs sources (soot collected from gasoline and diesel vehicle muffler, woodburning smoke), enables us to discriminate among the diverse sources of atmospheric PAHs. Soot PAHs extracted from gasoline and diesel vehicles show heavy isotopic signatures with a large inter-species {sup {delta}}1{sup 3C} variation from {sup -}12.9 per mille to {sup -}26.6 per mille, compared to soot PAHs extracted from woodburning smoke which are isotopically light, and have a small inter-species {sup {delta}}{sup 13}C variation from {sup -}26.8 per mille to -31.6 per mille. Values from -17.7 per mille to -27.9 per mille were obtained for the corresponding PAHs extracted from the smoke haze, indicating that they are derived mainly from automotive exhaust. Molecular and isotopic compositions of PAHs extracted from smoke haze were similar to those extracted from non-haze aerosol. Quantitative estimation shows that woodburning contribution to Malaysian atmospheric PAHs ranges from 25% to 35% with no relation to haze intensity, while automotive contribution ranges from 65% to 75%. These results suggest that the major contributor of PAHs in Malaysian air is automotive exhaust whether smoke haze is observed or not. (Author)

  6. Dust measurement campaign in the Mantes region atmosphere; Campagne de mesures ``poussieres`` dans l`atmosphere de la region Mantaise

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-12-31

    A measurement campaign have been carried out in the Mantes region (West of Paris) in order to determine particulate concentrations and types in the city atmosphere: granulometric particulate concentrations and concentration levels of the various types of airborne particulates (metals and metalloids, black smoke, polycyclic aromatic hydrocarbons, mono-cyclic aromatic hydrocarbons) are presented. The wind direction and speed have been taken into consideration

  7. Diurnal variations of residential particulate wood burning emissions and their contribution to the concentration of Polycyclic Aromatic Hydrocarbons (PAHs

    Directory of Open Access Journals (Sweden)

    L. Poulain

    2011-04-01

    Full Text Available Residential wood burning is becoming an increasingly important cause of air quality problems since it has become a popular source of alternative energy to fossil fuel. In order to characterize the contribution of residential wood burning to local particle pollution a field campaign was organized at the village of Seiffen (Saxony, Germany. During this campaign, an Aerosol Mass Spectrometer (AMS was deployed in parallel to a PM1 high volume filter sampler. The AMS mass spectra were analyzed using Positive Matrix Factorization (PMF to obtain detailed information about the organic aerosol (OA. Biomass-burning organic aerosol (BBOA, Hydrocarbon-like organic aerosol (HOA, Low-volatility oxygenated organic aerosol (LV-OOA and Semi-volatile oxygenated organic aerosol (SV-OOA were identified. Additionally, Polycyclic Aromatic Hydrocarbons (PAH were measured by the AMS and short term events of extremely high PAH concentration compared to the mean PAH value were observed during the whole measurement period. A comparison with the results from PM1 filter samples showed that the BBOA factor and the AMS PAH are good indicators of the total concentration of the different monosaccharide anhydrides and PAH measured on the filter samples. Based on its correlation with CO and the low car traffic, the HOA factor was considered to be related to residential heating using liquid fuel. A clear impact of the week and weekend days on the diurnal profiles of the different OA components was observed. The weekdays were characterized by two maxima; a first one early in the morning and a stronger one in the evening; during the weekend days, the different OA components principally reached one maxima early in the afternoon. Finally, the PAH emitted directly from residential wood combustion was estimated to represent 1.5% of the total mass of BBOA factor and around 62% of the total PAH concentration measured at Seiffen. This result highlights the important

  8. Rapid determination of trace polycyclic aromatic hydrocarbons in particulate matter using accelerated solvent extraction followed by ultra high performance liquid chromatography with fluorescence detection.

    Science.gov (United States)

    Xu, Tianci

    2016-05-01

    A method has been developed for the trace analysis of polycyclic aromatic hydrocarbons, which are known as persistent organic pollutants and ubiquitous constituents of fine particulate matter that causes growing airborne pollution. The method, which was especially for samples of airborne particulate matter less than 2.5 μm in diameter, utilized accelerated solvent extraction and ultra high performance liquid chromatography with fluorescence detector. Four principal parameters of accelerated solvent extraction were optimized to obtain maximum extraction efficiency. Using the established synergetic programs of gradient elution and fluorescence wavelength switching, a rapid separation was achieved in 6.56 min with good linearity for 15 polycyclic aromatic hydrocarbons (coefficient of determination above 0.999). The limits of detection ranged from 0.833 to 10.0 pg/m(3) . The precision of the method expressed as inter-day relative standard deviation ranged from 0.2 to 1%, which was calculated from nine repetitive measurements of 8.00 μg/L analytes. Average spiked recoveries ranged from 71.6 to 97.7%, with the exception of naphthalene. The rapid, sensitive, and accurate method can meet the pressing needs of health risk assessment and increasingly heavy daily tasks of air quality monitoring. PMID:26991966

  9. Atmospheric polycyclic aromatic hydrocarbons (PAHs) from post-harvest biomass burning emissions in the Indo-Gangetic Plain: Isomer ratios and temporal trends

    Science.gov (United States)

    Rajput, Prashant; Sarin, M. M.; Rengarajan, R.; Singh, Darshan

    2011-12-01

    Atmospheric concentrations of particulate polycyclic aromatic hydrocarbons (PAHs) and their isomer ratios have been studied for two distinct biomass burning emissions (post-harvest burning of paddy-residue in Oct-Nov and wheat-residue burning during April-May) in the Indo-Gangetic Plain (IGP). The mass concentrations of PM 2.5 (Av: 246 μg m -3), OC (92 μg m -3), EC (7 μg m -3) and ΣPAHs (40 ng m -3) are significantly higher from the paddy-residue burning. In contrast, for wheat-residue burning emissions, concentrations of PM 2.5 (53 μg m -3), OC (15 μg m -3), EC (4 μg m -3) and ΣPAHs (7 ng m -3) are about 4-5 times lower. The large temporal variability in the concentrations of particulate species and OC/EC ratio (range: 1.9-25.7) is attributed to differences in the two biomass burning emissions and their relative source strength. The mass fraction of EC (Av: 3.1%), associated with the poor combustion efficiency of moist paddy-residue, is significantly lower than that from the wheat-residue burning (EC/PM 2.5 = 7.6%) during dry weather conditions. Furthermore, OC mass fractions from paddy- and wheat-residue burning emissions are 37% and 28% respectively; whereas ΣPAHs/EC ratios are significantly different, 5.7 and 1.6 mg g -1, from the two emission sources. The particulate concentrations of 5- and 6-ring isomers (normalized to EC) from paddy-residue burning are about 3-5 times higher than those from the wheat-residue burning emissions. The cross plots of PAHs show distinct differences in isomer ratios from agricultural-waste burning emissions vis-à-vis fossil-fuel combustion.

  10. Global atmospheric emissions and transport of polycyclic aromatic hydrocarbons: Evaluation of modeling and transboundary pollution

    Science.gov (United States)

    Shen, Huizhong; Tao, Shu

    2014-05-01

    Global atmospheric emissions of 16 polycyclic aromatic hydrocarbons (PAHs) from 69 major sources were estimated for a period from 1960 to 2030. Regression models and a technology split method were used to estimated country and time specific emission factors, resulting in a new estimate of PAH emission factor variation among different countries and over time. PAH emissions in 2007 were spatially resolved to 0.1° × 0.1° grids based on a newly developed global high-resolution fuel combustion inventory (PKU-FUEL-2007). MOZART-4 (The Model for Ozone and Related Chemical Tracers, version 4) was applied to simulate the global tropospheric transport of Benzo(a)pyrene, one of the high molecular weight carcinogenic PAHs, at a horizontal resolution of 1.875° (longitude) × 1.8947° (latitude). The reaction with OH radical, gas/particle partitioning, wet deposition, dry deposition, and dynamic soil/ocean-air exchange of PAHs were considered. The simulation was validated by observations at both background and non-background sites, including Alert site in Canadian High Arctic, EMEP sites in Europe, and other 254 urban/rural sites reported from literatures. Key factors effecting long-range transport of BaP were addressed, and transboundary pollution was discussed.

  11. Orange jasmine leaves as an indicator of atmospheric polycyclic aromatic hydrocarbons

    Directory of Open Access Journals (Sweden)

    Benjalak Karnchanasest

    2005-07-01

    Full Text Available Sorption of atmospheric PAHs in orange jasmine leaves, Murraya paniculata (L. Jack and the potential of leaves to indicate atmospheric PAHs were investigated. Partitioning experiments between leaves and water were conducted to determine the partition coefficients of the compounds between the leaves and the water. The leaf samples were collected on 4 Bangkok roadsides, where the air samples were measured for 24 h using high volume, to analyze 16 PAHs. The actual measured PAH concentrations were compared to atmospheric concentrations calculated from the leaf/air partition coefficients and PAH leaf concentrations. It was found that they were well related as indicated by correlation coefficient (r2 > 0.70, particularly low molecular weight (MW PAHs, which were ACY, ACE, FLU, PHE and ANT. This was because low MW PAHs were mostly present in gas phase, which played a major role in leaf sorption. Therefore, high MW PAHs, existing mainly in particulate phase, exhibited lower correlation coefficient (r2 < 0.60.

  12. Polycyclic aromatic hydrocarbon concentrations in gas and particle phases and source determination in atmospheric samples from a semiurban area of Dourados, Brazil.

    Science.gov (United States)

    Ré, Nilva; Kataoka, Vanessa Mayumi Fukuy; Cardoso, Claudia Andrea Lima; Alcantara, Glaucia Braz; de Souza, João Batista Gomes

    2015-07-01

    A headspace solid-phase microextraction (HS-SPME) procedure that employs a PDMS/DVB fiber was developed for the analysis of gas-phase polycyclic aromatic hydrocarbons (PAHs) collected in polyurethane foam (PUF) by gas chromatography (GC) mass spectrometry. The method exhibited good linearity (R (2) > 0.99) and repeatability (4.9-25 %) as well as an impressive detection limit that ranged from 1.1 to 3.3 ng. Twenty-two air samples were collected by high-volume samplers from January to November 2007 in a semiurban area of Dourados (Brazil) and were analyzed for their content of total suspended particulates and PAHs. The PAHs were extracted from the PUF samples using the developed procedure (HS-SPME), and PAHs adsorbed on particulate matter were extracted with dichloromethane/methanol (4:1 [v/v]) in an ultrasonic bath. The values of the total daily concentrations of 16 PAHs determined in the samples ranged from 0.375 to 8.407 ng m(-3). In addition, diagnostic ratios were calculated, showing that the PAHs in the atmosphere at the sampling site originated predominantly from vehicle emissions and the combustion of grass and wood. Hierarchical cluster analysis and principal component analysis were performed as well, the results of which indicated (1) the same sources of PAH identified by the diagnostic ratios and (2) that the sampling days could be categorized into three groups depending on the atmospheric conditions. GC retention indices were also used to identify PAHs, biphenyl (phenylbenzene), and heterocyclic organic compounds (benzofurans) in some of the samples. PMID:25851064

  13. [Geochemical characteristics and sources of atmospheric particulates in Shanghai during dust storm event].

    Science.gov (United States)

    Qian, Peng; Zheng, Xiang-min; Zhou, Li-min

    2013-05-01

    Atmospheric particulates were sampled from three sampling sites of Putuo, Minhang and Qingpu Districts in Shanghai between Oct. , 2009 and Oct. , 2010. In addition, particulate samples were also collected from Nantong, Zhengzhou, Xi'an, and Beijing city where dust storm dust transported along during spring. Element compositions of atmospheric particulates were determined by XRF and ICP-MS. The concentrations of major and trace elements in atmospheric particulates from Putuo, Minhang and Qingpu Districts were similar, indicating their common source. The UCC standardization distribution map showed that the major element composition of dust storm samples was similar to that of loess in northwestern China, indicating that the dust storm dust was mainly derived from Western desert and partly from local area. The REE partition patterns of dust storm dusts among different cities along dust transport route were similar to each other, as well as to those of northern loess, which indicates that the dust storm samples may have the same material source as loess, which mainly comes from crust material. However, the REE partition patterns of non-dust storm particulates were different among the studied cities, and different from those of loess, which suggests that the non-dust storm samples may be mixed with non-crust source material, which is different from dust storm dust and loess. The major element composition and REE partition pattern are effective indicators for source tracing of dust storm dust. PMID:23914561

  14. 40 CFR Appendix B to Part 50 - Reference Method for the Determination of Suspended Particulate Matter in the Atmosphere (High...

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 2 2010-07-01 2010-07-01 false Reference Method for the Determination of Suspended Particulate Matter in the Atmosphere (High-Volume Method) B Appendix B to Part 50... Determination of Suspended Particulate Matter in the Atmosphere (High-Volume Method) 1.0 Applicability. 1.1...

  15. Modelling Chemical Patterns of Atmospheric Polycyclic Aromatic Hydrocarbons (PAHs) in the Iberian Peninsula

    Science.gov (United States)

    Ratola, Nuno; Jiménez-Guerrero, Pedro

    2013-04-01

    Semi-volatile organic compounds (SVOCs) such as PBDEs, PCBs, organochlorine pesticides (OCPs) or PAHs, are widespread and generated in a multitude of anthropogenic (and natural for PAHs) processes and although they are found in the environment at low concentrations, possess an extraordinary carcinogenic capacity (Baussant et al., 2001) and high ecotoxicity due to their persistence in different matrices (air, soil, water, living organisms). In particular, PAHs are originated by combustion processes or release from fossil fuels and can be transported in the atmosphere over long distances in gaseous or particulate matter (Baek et al., 1991). The establishment of strategies for sampling and chemical transport modelling of SVOCs in the atmosphere aiming the definition and validation of the spatial, temporal and chemical transport patterns of contaminants can be achieved by an integrated system of third-generation models that represent the current state of knowledge in air quality modelling and experimental data collected in field campaigns. This has implications in the fields of meteorology, atmospheric chemistry and even climate change. In this case, an extensive database already obtained on levels of atmospheric PAHs from biomonitoring schemes in the Iberian Peninsula fuelled the establishment of the first models of behaviour for PAHs. The modelling system WRF+CHIMERE was implemented with high spatial and temporal resolution to the Iberian Peninsula in this first task (9 km for the Iberian Peninsula, 3 km to Portugal, 1 hour), using PAHs atmospheric levels collected over a year-long sampling scheme comprising 4 campaigns (one per season) in over 30 sites. Daily information on meteorological parameters such as air temperature, humidity, rainfall or wind speed and direction was collected from the weather stations closest to the sampling sites. Diagnosis and forecasts of these meteorological variables using MM5 or WRF were used to feed a chemistry transport model

  16. Long-range atmospheric transport and the distribution of polycyclic aromatic hydrocarbons in Changbai Mountain.

    Science.gov (United States)

    Zhao, Xiangai; Kim, Seung-Kyu; Zhu, Weihong; Kannan, Narayanan; Li, Donghao

    2015-01-01

    The Changbai (also known as "Baekdu") Mountain, on the border between China and North Korea, is the highest mountain (2750 m) in northeastern China. Recently, this mountain region has experienced a dramatic increase in air pollution, not only because of increasing volumes of tourism-derived traffic but also because of the long-range transport of polluted westerly winds passing through major industrial and urban cities in the eastern region of China. To assess the relative importance of the two sources of pollution, 16 polycyclic aromatic hydrocarbons (PAHs) as model substances were determined in the mountain soil. A total of 32 soil samples were collected from different sides of the mountain at different latitudes between July and August of 2009. The ∑PAH concentrations were within the range 38.5-190.1 ng g(-1) on the northern side, 117.7-443.6 ng g(-1) on the southern side, and 75.3-437.3 ng g(-1) on the western side. A progressive increase in the level of ∑PAHs with latitude was observed on the southern and western sides that face the westerly wind with abundant precipitation. However, a similar concentration gradient was not observed on the northern side that receives less rain and is on the leeward direction of the wind. The high-molecular-weight PAH compounds were predominant in the soils on the southern and western sides, while low-molecular-weight PAHs dominated the northern side soils. These findings show that the distribution of PAHs in the mountain soil is strongly influenced by the atmospheric long-range transport and cold trapping. PMID:25036943

  17. Characteristics and sources of polycyclic aromatic hydrocarbons in atmospheric aerosols in the Kathmandu Valley, Nepal.

    Science.gov (United States)

    Chen, Pengfei; Kang, Shichang; Li, Chaoliu; Rupakheti, Maheswar; Yan, Fangping; Li, Quanlian; Ji, Zhenming; Zhang, Qianggong; Luo, Wei; Sillanpää, Mika

    2015-12-15

    The Kathmandu Valley in the foothills of the Himalayas, where the capital city of Nepal is located, has one of the most serious air pollution problems in the world. In this study, total suspended particle (TSP) samples collected over a year (April 2013-March 2014) in the Kathmandu Valley were analyzed for determining the concentrations of 15 priority particle-bound polycyclic aromatic hydrocarbons (PAHs). The TSP and PAH concentrations were extremely high, with annual average concentration being 199±124μg/m(3) and 155±130ng/m(3), respectively, which are comparable to those observed in Asian cities such as Beijing and Delhi. The TSP and PAH concentrations varied considerably, with the seasonal average concentration being maximal during the post-monsoon season followed by, in descending order, the winter, pre-monsoon, and monsoon seasons. In the winter and pre-monsoon seasons, ambient TSP and PAH concentrations increased because of emissions from brick kilns and the use of numerous small generators. Moreover, in the pre-monsoon season, forest fires in the surrounding regions influenced the TSP and PAH concentrations in the valley. PAHs with 4 to 6 rings constituted a predominant proportion (92.3-93.3%) of the total PAHs throughout the year. Evaluation of diagnostic molecular ratios indicated that the atmospheric PAHs in the Kathmandu Valley originated mainly from diesel and biomass combustion. The toxic equivalent quantity (TEQ) of particle phase PAHs ranged between 2.74 and 81.5ngTEQ/m(3), which is considerably higher than those reported in other South Asian cities, and 2-80 times higher than the World Health Organization guideline (1ngTEQ/m(3)). This suggests that ambient PAH levels in the Kathmandu Valley pose a serious health risk to its approximately 3.5 million residents. PMID:26298251

  18. Interaction of DNA with aromatic hydrocarbons fraction in atmospheric particulates of Xigu District of Lanzhou, China

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Voluminously epidemiological studies show that the relationships exist between the air pollution and human health and cancer. Aromatic hydrocarbons (AHs) in air form a large class of organic pollutants, which are widely in environment and many of them are known to be carcinogenic and/or mutagenic and contribute to ambient air pollution. In the past decades, bioassays mainly have been used to evaluate the toxicity of chemical mixtures in atmospheric particulates or aqueous environment. However, it is well known that the covalent complexes formed by carcinogens with DNA may be exert negative results in bioassay. So the main aim of this paper is to develop an evaluation method of toxicity effects of chemical mixtures in atmospheric particulates from chemical standpoint. In this study, the in virto interaction of the AHs with DNA was investigated by absorption, fluorescence and resonance light scattering (RLS) spectroscopic techniques. The results showed that the AHs in the atmospheric particulates could combine with calf thymus DNA (ctDNA) and herring sperm DNA (hsDNA) without being activated or metabolized by organism, respectively. Intercalation may be present in the mechanism of interaction. The binding constants of the AHs with ctDNA and hsDNA were 2.5×102 and 2.0×103, respectively, which indicated that the interaction of the AHs with hsDNA is stronger than that with ctDNA. In addition, the relationships of dose-effect between the total mole concentration of chemical components and the ability of binding ct DNA and hsDNA were confirmed. This research made it possible to study the toxicity effects of chemical mixtures in atmospheric particulates by chemical method. It is believed that the composition and contents of unknown AHs and the interaction of DNA with AHs in atmospheric particulates of Xigu District of Lanzhou City, China are first reported in the past twenty years.

  19. Sources of atmospheric carbonaceous particulate matter in Pittsburgh, Pennsylvania

    Energy Technology Data Exchange (ETDEWEB)

    Cabada, J.C.; Pandis, S.N.; Robinson, A.L. [Carnegie Mellon University, Pittsburgh, PA (United States)

    2002-06-01

    The organic carbon (OC)/elemental carbon (EC) tracer method is applied to the Pittsburgh, PA, area to estimate the contribution of secondary organic aerosol (SOA) to the monthly average concentration of organic particulate matter (PM) during 1995. An emissions inventory is constructed for the primary emissions of OC and EC in the area of interest. The ratio of primary emissions of OC to those of EC ranges between 2.4 in the winter months and 1.0 in summer months. A mass balance model and ambient measurements were used to assess the accuracy of the emissions inventory. It is estimated to be accurate to within 50%. The results from this analysis show a strong monthly dependence of the SOA contribution to the total organic PM concentration, varying from near zero during winter months to as much as 50% of the total OC concentration in the summer. Local wood and fugitive sources combustion are major sources of primary OC in western Pennsylvania on an annual basis (33 and 22% respectively), and wood burning is the dominant source during winter months. The coke producing industry and diesel combustion are the dominant sources of the primary EC emissions (21 and 30% respectively). The EC emissions show a weaker monthly dependence compared with that shown by OC sources. 57 refs., 9 figs., 8 tabs.

  20. Global atmospheric emissions of polycyclic aromatic hydrocarbons from 1960 to 2008 and future predictions.

    Science.gov (United States)

    Shen, Huizhong; Huang, Ye; Wang, Rong; Zhu, Dan; Li, Wei; Shen, Guofeng; Wang, Bin; Zhang, Yanyan; Chen, Yuanchen; Lu, Yan; Chen, Han; Li, Tongchao; Sun, Kang; Li, Bengang; Liu, Wenxin; Liu, Junfeng; Tao, Shu

    2013-06-18

    Global atmospheric emissions of 16 polycyclic aromatic hydrocarbons (PAHs) from 69 major sources were estimated for a period from 1960 to 2030. Regression models and a technology split method were used to estimate country and time specific emission factors, resulting in a new estimate of PAH emission factor variation among different countries and over time. PAH emissions in 2007 were spatially resolved to 0.1° × 0.1° grids based on a newly developed global high-resolution fuel combustion inventory (PKU-FUEL-2007). The global total annual atmospheric emission of 16 PAHs in 2007 was 504 Gg (331-818 Gg, as interquartile range), with residential/commercial biomass burning (60.5%), open-field biomass burning (agricultural waste burning, deforestation, and wildfire, 13.6%), and petroleum consumption by on-road motor vehicles (12.8%) as the major sources. South (87 Gg), East (111 Gg), and Southeast Asia (52 Gg) were the regions with the highest PAH emission densities, contributing half of the global total PAH emissions. Among the global total PAH emissions, 6.19% of the emissions were in the form of high molecular weight carcinogenic compounds and the percentage of the carcinogenic PAHs was higher in developing countries (6.22%) than in developed countries (5.73%), due to the differences in energy structures and the disparities of technology. The potential health impact of the PAH emissions was greatest in the parts of the world with high anthropogenic PAH emissions, because of the overlap of the high emissions and high population densities. Global total PAH emissions peaked at 592 Gg in 1995 and declined gradually to 499 Gg in 2008. Total PAH emissions from developed countries peaked at 122 Gg in the early 1970s and decreased to 38 Gg in 2008. Simulation of PAH emissions from 2009 to 2030 revealed that PAH emissions in developed and developing countries would decrease by 46-71% and 48-64%, respectively, based on the six IPCC SRES scenarios. PMID:23659377

  1. Heterogeneous Reactions of Particulate Matter-Bound PAHs and NPAHs with NO3/N2O5, OH Radicals, and O3 under Simulated Long-Range Atmospheric Transport Conditions: Reactivity and Mutagenicity

    OpenAIRE

    JARIYASOPIT, NARUMOL; Zimmermann, Kathryn; Schrlau, Jill; AREY, JANET; Atkinson, Roger; Yu, Tian-Wei; Dashwood, Roderick H.; Tao, Shu; Simonich, Staci L. Massey

    2014-01-01

    The heterogeneous reactions of ambient particulate matter (PM)-bound polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs (NPAHs) with NO3/N2O5, OH radicals, and O3 were studied in a laboratory photochemical chamber. Ambient PM2.5 and PM10 samples were collected from Beijing, China, and Riverside, California, and exposed under simulated atmospheric long-range transport conditions for O3 and OH and NO3 radicals. Changes in the masses of 23 PAHs and 20 NPAHs, as well as the direct and indirec...

  2. Determination of metals in atmospheric particulates using atomic absorption spectrometry

    International Nuclear Information System (INIS)

    Nineteen trace metals in atmospheric samples have been determined by atomic absorption spectrometry, using a graphite furnace for most elements. Paper filters have been used to collect air samples. The sample preparation procedure involves the removal of organic matter and the conversion of the metals to soluble salts by ashing the filters in an oxygen plasma at 125 deg C for 6 h. and by subsequent dissolution in HN03HCl solution. The sensitivities achieved are in the range of 2,5.10-5 and 6,3.10-3 μg/m3, for an air volume of 2000 m3. (author)

  3. Evaluation of atmospheric particulate concentrations derived from analysis of ratio Thematic Mapper data

    Science.gov (United States)

    Carnahan, W. H.; Mausel, P. W.; Zhou, G. P.

    1984-01-01

    An approach for atmospheric particulate concentration evaluation above urban areas using ratio Thematic Mapper (TM) data is discussed. October 25, 1982 TM data over Chicago, IL are analyzed using TM band ratios of 1/2, 1/3, 1/4, 1/5, and 1/6 and particulate concentration estimates derived from TM ratios are tested over low reflective turbid water sites and highly reflective concrete highways. From analysis of the data it is evident that for water, the pattern of increasing particulate concentration is associated with decreasing ratio values in all band combinations used. Over concrete features, the TM band 1/4 ratio values follow the predicted pattern, while the TM band 1/6 has ratios which are reversed from anticipated values.

  4. 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 samples collected during the whole study period showed statistically significant differences for particulate 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

  5. Characterization of polycyclic aromatic hydrocarbon emissions in the particulate and gas phase from smoldering mosquito coils containing various atomic hydrogen/carbon ratios

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Tzu-Ting, E-mail: d89844001@ntu.edu.tw [Department of Environmental Engineering and Health, Yuanpei University, No. 306, Yuanpei St., Hsin Chu 30015, Taiwan (China); Lin, Shaw-Tao [Department of Applied Chemistry, Providence University, No. 200 Chung-Chi Rd., Salu Dist., Taichung City 43301, Taiwan (China); Lin, Tser-Sheng [Department of Safety, Health, and Environmental Engineering, National United University, 2 Lien Da, Maioli 360, Taiwan (China); Chung, Hua-Yi [Department of Environmental Engineering and Health, Yuanpei University, No. 306, Yuanpei St., Hsin Chu 30015, Taiwan (China)

    2015-02-15

    The polycyclic aromatic hydrocarbon emissions in particulate and gas phases generated from smoldering mosquito coils containing various atomic H/C ratios were examined. Five types of mosquito coils were burned in a test chamber with a total airflow rate of 8.0 L/min at a constant relative humidity and temperature. The concentrations of individual PAHs were determined using the GC/MS technique. Among the used mosquito coils, the atomic H/C ratio ranged from 1.23 to 1.57, yielding total mass, gaseous, and particulate PAH emission factors of 28.17–78.72 mg/g, 26,139.80–35,932.98 and 5735.22–13,431.51 ng/g, respectively. The various partitions of PAHs in the gaseous and particulate phases were in the ranges, 70.26–83.70% and 16.30–29.74% for the utilized mosquito coils. The carcinogenic potency of PAH emissions in the particulate phase (203.82–797.76 ng/g) was approximately 6.92–25.08 times higher than that of the gaseous phase (26.27–36.07 ng/g). Based on the analyses of PAH emissions, mosquito coils containing the lowest H/C ratio, a low oxygen level, and additional additives (i.e., CaCO{sub 3}) are recommended for minimizing the production of total PAH emission factors and carcinogenic potency. - Highlights: • PAHs emissions are influenced by mosquito coils containing various atomic H/C ratios. • The PAHs generated by burning mosquito coils mainly occur in the gaseous phase. • Total TEQ emission factors of PAHs mainly consisted of the particulate phase (> 87%). • The BaP and BaA accounted for 71.13–77.28% of the total TEQ emission factors. • Special PAH ratios were regarded as characteristic ratios for burning mosquito coil.

  6. Elemental compositions of atmospheric particulates collected in Japan in 2002 to 2004

    International Nuclear Information System (INIS)

    Recently, fine SPM (atmospheric suspended particulate matter) is concerned for its impact to human heath. In USA, concentration of fine SPM, PM2.5, in the atmosphere is regulated legally. In the Metropolitan area of Japan, concentration of particulate matter in exhaust from diesel cars, which is one of major sources of PM2.5, is regulated. We have been collecting SPM at Hachioji and Sakata in Japan from 2002 and determining elemental concentrations in SPM by nuclear analytical methods. In this study, elemental characteristics of SPM collected at Hachioji and at Sakata in Japan from 2002 to 2004 are described. Atmospheric particulates were collected using NILU filter holder included PM10 inlet and two Nuclepore polycarbonate filters of different pore sizes (8.0 μm and 0.4 μm) at Hachioji and Sakata, Japan. Hachioji is an urban area and about 40 km west to the center of Tokyo. Sakata is a rural area and faces to the Japan Sea. Polycarbonate filters with SPM were cut in half. One half was folded in square- (10 mm x 10 mm), and was firstly subjected to prompt gamma-ray analysis (PGA). Then, INAA was performed for the same sample as used for PGA. In INAA, elemental concentrations were determined by ko standardization method. Mean particulate concentrations of coarse and fine particulates were 15 and 14 g/m3 at Hachioji, and 9.4 and 9.7 g/m3 at Sakata, respectively. And mean weight ratios (fine/coarse) were 1.0 and 1.5 for Hachioji and Sakata, respectively. At Sakata, high particulate concentrations caused by the yellow sand storm were observed in March and April in 2002. About 40 elemental concentrations in SPM were determined by PGA and INAA. Mean elemental concentration values for 3 years vary from ∼l03 ng/m3 for S to ∼10-3 ng/m3 for Au. The concentration level of coarse and fine particulates for most elements are not largely different between the two cities, except for several elements. It was found that concentrations of some elements such as Ag, Cu, and W

  7. 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.

  8. Elemental compositions of atmospheric particulates collected in Japan from 2002 to 2004

    International Nuclear Information System (INIS)

    Chemical compositions of suspended particulate matter (SPM) in atmosphere collected at Hachioji and Sakata in Japan from 2002 to 2004 were determined by prompt gamma-ray analysis and instrumental neutron activation analysis. About 40 elemental concentrations in SPM could be determined, and enrichment factors and elemental correlations were examined. Several elements such as Cl, Cr, Ag, Sb, and W were largely different between Hachioji and Sakata, although their sources are not clear at present. (author)

  9. Losses of arsenic during the low temperature ashing of atmospheric particulate samples

    International Nuclear Information System (INIS)

    Neutron activation and atomic absorption procedures have been used to study arsenic losses during low temperature ashing at power levels between 50 and 125 watts (RF). Losses of arsenic from ambient atmospheric particulate matter and various synthetic sea salt matrices containing known quantities of arsenic was observed. In general, the magnitude of arsenic losses by this treatment will depend on applied power levels and the physical and chemical properties of the arsenic sample matrix

  10. Interactions between Atmospheric Particulate Matter and Stone Surfaces by Means of Laboratory and Field Studies

    OpenAIRE

    CASATI, M.

    2016-01-01

    The PhD work is focused on the interactions between atmospheric particulate matter (PM) and stone surfaces, particularly with reference to the decay phenomena that can happen as a consequence of PM deposition. Laboratory studies have been focused on the relationship between PM’s chemical composition and the decay hazards to which the stone surfaces subjected to PM deposition are exposed. A new evaluation method has been proposed. The method exploits experimental measurements of deliquescence ...

  11. Development of analytical methodologies for iodine species in gaseous and particulate phases of the coastal atmosphere

    OpenAIRE

    Chen, Hongwei

    2005-01-01

    It has been demonstrated that iodine does have an important influence on atmospheric chemistry, especially the formation of new particles and the enrichment of iodine in marine aerosols. It was pointed out that the most probable chemical species involved in the production or growth of these particles are iodine oxides, produced photochemically from biogenic halocarbon emissions and/or iodine emission from the sea surface. However, the iodine chemistry from gaseous to particulate phase in the ...

  12. Remote sensing of atmospheric particulates: Technological innovation and physical limitations in applications to short-range weather prediction

    Science.gov (United States)

    Curran, R. J.; Kropfil, R.; Hallett, J.

    1984-01-01

    Techniques for remote sensing of particles, from cloud droplet to hailstone size, using optical and microwave frequencies are reviewed. The inherent variability of atmospheric particulates is examined to delineate conditions when the signal can give information to be effectively utilized in a forecasting context. The physical limitations resulting from the phase, size, orientation and concentration variability of the particulates are assessed.

  13. Emissions of particulate matter and associated polycyclic aromatic hydrocarbons from agricultural diesel engine fueled with degummed,deacidified mixed crude palm oil blends

    Institute of Scientific and Technical Information of China (English)

    Khamphe Phoungthong; Surajit Tekasakul; Perapong Tekasakul; Gumpon Prateepchaikul; Naret Jindapetch; Masami Furuuchi; Mitsuhiko Hata

    2013-01-01

    Mixed crude palm oil (MCPO),the mixture of palm fiber oil and palm kernel oil,has become of great interest as a renewable energy source.It can be easily extracted from whole dried palm fruits.In the present work,the degummed,deacidified MCPO was blended in petroleum diesel at portions of 30% and 40% by volume and then tested in agricultural diesel engines for long term usage.The particulates from the exhaust of the engines were collected every 500 hr using a four-stage cascade air sampler.The 50% cut-off aerodynamic diameters for the first three stages were 10,2.5 and 1 μm,while the last stage collected all particles smaller than 1 μm.Sixteen particle bounded polycyclic aromatic hydrocarbons (PAHs) were analyzed using a high performance liquid chromatography.The results indicated that the size distribution of particulate matter was in the accumulation mode and the pattern of total PAHs associated with fine-particles (< 1 μm) showed a dominance of larger molecular weight PAHs (4-6 aromatic rings),especially pyrene.The mass median diameter,PM and total PAH concentrations decreased when increasing the palm oil content,but increased when the running hours of the engine were increased.In addition,Commercial petroleum diesel (PB0) gave the highest value of carcinogenic potency equivalent (BaPeq) for all particle size ranges.As the palm oil was increased,the BaPeq decreased gradually.Therefore the degummed-deacidified MCPO blends are recommended for diesel substitute.

  14. [Analyzer Design of Atmospheric Particulate Matter's Concentration and Elemental Composition Based on β and X-Ray's Analysis Techniques].

    Science.gov (United States)

    Ge, Liang-quan; Liu, He-fan; Zeng, Guo-qiang; Zhang, Qing-xian; Ren, Mao-qiang; Li, Dan; Gu, Yi; Luo, Yao-yao; Zhao, Jian-kun

    2016-03-01

    Monitoring atmospheric particulate matter requires real-time analysis, such as particulate matter's concentrations, their element types and contents. An analyzer which is based on β and X rays analysis techniques is designed to meet those demands. Applying β-ray attenuation law and energy dispersive X-ray fluorescence analysis principle, the paper introduces the analyzer's overall design scheme, structure, FPGA circuit hardware and software for the analyzer. And the analyzer can measure atmospheric particulate matters' concentration, elements and their contents by on-line analysis. Pure elemental particle standard samples were prepared by deposition, and those standard samples were used to set the calibration for the analyzer in this paper. The analyzer can monitor atmospheric particulate matters concentration, 30 kinds of elements and content, such as TSP, PM10 and PM2.5. Comparing the measurement results from the analyzer to Chengdu Environmental Protection Agency's monitoring results for monitoring particulate matters, a high consistency is obtained by the application in eastern suburbs of Chengdu. Meanwhile, the analyzer are highly sensitive in monitoring particulate matters which contained heavy metal elements (such as As, Hg, Cd, Cr, Pb and so on). The analyzer has lots of characteristics through technical performance testing, such as continuous measurement, low detection limit, quick analysis, easy to use and so on. In conclusion, the analyzer can meet the demands for analyzing atmospheric particulate matter's concentration, elements and their contents in urban environmental monitoring. PMID:27400540

  15. Inhibition of the WNT/β-catenin pathway by fine particulate matter in haze: Roles of metals and polycyclic aromatic hydrocarbons

    Science.gov (United States)

    Lee, Kang-Yun; Cao, Jun-Ji; Lee, Chii-Hong; Hsiao, Ta-Chih; Yeh, Chi-Tai; Huynh, Thanh-Tuan; Han, Yong-Ming; Li, Xiang-Dong; Chuang, Kai-Jen; Tian, Linwei; Ho, Kin-Fai; Chuang, Hsiao-Chi

    2015-05-01

    Air pollution might have a great impact on pulmonary health, but biological evidence in response to particulate matter less than 2.5 μm in size (PM2.5) has been lacking. Physicochemical characterization of haze PM2.5 collected from Beijing, Xian and Hong Kong was performed. Biological pathways were identified by proteomic profiling in mouse lungs, suggesting that WNT/β-catenin is important in the response to haze PM2.5. Suppression of β-catenin levels, activation of caspase-3 and alveolar destruction, as well as IL-6, TNF-α and IFN-γ production, were observed in the lungs. The inhibition of β-catenin, TCF4 and cyclin D1 was observed in vitro in response to haze PM2.5. The inhibition of WNT/β-catenin signaling, apoptosis-related results (caspase-3 and alveolar destruction), and inflammation, particularly including caspase-3 and alveolar destruction, were more highly associated with polycyclic aromatic hydrocarbons in haze PM2.5. In conclusion, decreased WNT/β-catenin expression modulated by haze PM2.5 could be involved in alveolar destruction and inflammation during haze episodes.

  16. Co-firing coal with rice husk and bamboo and the impact on particulate matters and associated polycyclic aromatic hydrocarbon emissions.

    Science.gov (United States)

    Chao, Christopher Y H; Kwong, Philip C W; Wang, J H; Cheung, C W; Kendall, Gail

    2008-01-01

    The potential of co-firing rice husk and bamboo with coal was studied in a bench-scale pulverized fuel combustion reactor. Experimental parameters including biomass blending ratio in the fuel mixture, biomass grinding size, excess air ratio and relative moisture content in the biomass were investigated. Particulate Matters in the forms of PM(10), PM(2.1), ultra fine particles as well as the associated Polycyclic Aromatic Hydrocarbons (PAHs) emissions were evaluated. An operation range between 10% and 30% of biomass to coal ratio was found to be the optimum range in terms of minimum pollutant emissions per unit energy output. Co-combustion of coal with biomass seemed to have the effect of moving the fly-ash in PM(2.1) to a larger size range, but increasing the number counts of the ultra fine particles. It was noted that the much higher volatile matter content in the biomass fuels has played a key role in improving the combustion performance in the system. However, slagging, fouling and formation of clinker could be the issues requiring attention when using biomass co-combustion in conventional boilers. PMID:17257831

  17. A critical and comparative appraisal of polycyclic aromatic hydrocarbons in sediments and suspended particulate material from a large South American subtropical estuary.

    Science.gov (United States)

    Cardoso, Fernanda D; Dauner, Ana Lúcia L; Martins, César C

    2016-07-01

    The Paranaguá Estuarine Complex (PEC) is an important socioeconomic estuary of the Brazilian coast that is influenced by the input of pollutants like polycyclic aromatic hydrocarbons (PAHs). Because of the apparent lack of comparative studies involving PAHs in different estuarine compartments, the aim of this study was to determine and compare PAH concentrations in surface sediment and suspended particulate material (SPM) in the PEC to evaluate their behaviour, compositions, sources and spatial distributions. The total PAH concentrations in the sediment ranged from 0.6 to 63.8 ng g(-1) (dry weight), whereas in the SPM these concentrations ranged from 391 to 4164 ng g(-1). Diagnostic ratios suggest distinct sources of PAHs to sediments (i.e., pyrolytic sources) and SPM (i.e., petrogenic sources such as vessel traffic). Thus, the recent introduction of PAHs is more clearly indicated in the SPM since oil related-compounds (e.g., alkyl-PAHs) remain present in similar concentrations. Further, this matrix may better reflect the current state of the environment at the time of sampling because of the absence of significant degradation. PMID:27089419

  18. Indoor-outdoor levels of size segregated particulate matter and mono/polycyclic aromatic hydrocarbons among urban areas using solid fuels for heating

    Science.gov (United States)

    Kliucininkas, Linas; Krugly, Edvinas; Stasiulaitiene, Inga; Radziuniene, Inga; Prasauskas, Tadas; Jonusas, Arunas; Kauneliene, Violeta; Martuzevicius, Dainius

    2014-11-01

    Emissions from the fuel combustion in the energy production are causes of concern due to associated health risks, but little information is available on the impact of residential fuel burning on indoor air quality, where most of the human exposure occurs. In this complex study, concentrations of size-segregated particulate matter (PM), monocyclic and polycyclic aromatic compounds (MAHs and PAHs) at indoor and outdoor sites in six urban homes in the city of Kaunas, Lithuania, were determined over winter and summer sampling campaigns, specifically targeting the impact of the local fuel burning to the indoor air quality. PM levels observed in Kaunas during winter measurement campaign were higher compared to those in many other European settlements utilizing biomass for energy production. The particle size distribution analysis revealed that the major part of the PM mass in winter period consisted of fine particles (PM2.5). Both MAH and PAH levels were higher in winter. The indoor to outdoor ratios (I/O) of MAHs and PAHs revealed specific patterns depending on the presence of emissions sources indoors. Irrespectively of the season, I/O values were <1, suggesting that in case of the absence of an indoor pollution, the dominant source of organic compounds was from the outdoor environment. In homes with no PAH source inside, the I/O ratio equalled ranged from 0.05 to 0.36, suggesting the penetrated portion of outdoor combustion particles to the indoor air.

  19. Canadian and U.S. sources impacting the mercury levels in fine atmospheric particulate material across New York state

    Energy Technology Data Exchange (ETDEWEB)

    Olmez, I.; Ames, M.R.; Gullu, G. [Massachusetts Inst. of Tech., Cambridge, MA (United States). Nuclear Reactor Lab.

    1998-10-15

    An extensive atmospheric sampling and analysis program has been completed in order to identify and apportion the sources of mercury associated with fine atmospheric particulate material. Samples of fine atmospheric particulate material were collected daily, at five remote sites in New York State, over a period of 2 years. The trace element composition of 1200 of these samples was determined by Instrumental Neutron Activation Analysis. Results of both meteorological and statistical analyses of the data indicate that approximately 55% of the fine particulate mercury originated from smelters in Ontario and Quebec, and 25% originated from a mixture of regional sources in the Midwestern United States. A decline in the average measured particulate Hg concentration, beginning in February 1993, has been attributed to reduced emissions from one or more of the major Canadian smelters.

  20. The Influence of Sandstorms and Long-Range Transport on Polycyclic Aromatic Hydrocarbons (PAHs in PM2.5 in the High-Altitude Atmosphere of Southern China

    Directory of Open Access Journals (Sweden)

    Minmin Yang

    2015-10-01

    Full Text Available PM2.5 (Particulate Matter 2.5 samples were collected at Mount Heng and analyzed for polycyclic aromatic hydrocarbons (PAHs. During sampling, a sandstorm from northern China struck Mount Heng and resulted in a mean PM2.5 concentration of 150.61 μg/m3, which greatly exceeded the concentration measured under normal conditions (no sandstorm: 58.50 μg/m3. The average mass of PAHs in PM2.5 was 30.70 μg/g, which was much lower than in the non-sandstorm samples (80.80 μg/g. Therefore, the sandstorm increased particle levels but decreased PAH concentrations due to dilution and turbulence. During the sandstorm, the concentrations of 4- and 5-ring PAHs were below their detection limits, and 6-ring PAHs were the most abundant. Under normal conditions, the concentrations of 2-, 3- and 6-ring PAHs were higher, and 4- and 5-ring PAHs were lower relative to the other sampling sites. In general, the PAH contamination was low to medium at Mount Heng. Higher LMW (low molecular weight concentrations were primarily linked to meteorological conditions, and higher HMW (high molecular weight concentrations primarily resulted from long-range transport. Analysis of diagnostic ratios indicated that PM2.5 PAHs had been emitted during the combustion of coal, wood or petroleum. The transport characteristics and origins of the PAHs were investigated using backwards Lagrangian particle dispersion modeling. Under normal conditions, the “footprint” retroplumes and potential source contributions of PAHs for the highest and lowest concentrations indicated that local sources had little effect. In contrast, long-range transport played a vital role in the levels of PM2.5 and PAHs in the high-altitude atmosphere.

  1. Determination of polycyclic aromatic hydrocarbons in Metro Manila air particulate by high performance liquid chromatography with fluorescence detection

    International Nuclear Information System (INIS)

    The development of analytical procedures for the determination of PAHs in air particulates is described. The optimized methodology consisted of the following: Samples were extracted by Soxhlet for 16 hours with cylclohexane, followed by concentration of the extract under reduced pressure in a rotary evaporator. Clean-up was done by passing the extract through a Seppak silica cartridge and eluting with chloroform. Analysis was performed by HPLC with fluorescence detection. The analytes determined were anthracene, fluoranthene, benzo(a)pyrene,dibenz(a,h)anthracence, and benzo(g,h,i) perylene. Detection limits were lowest for benzo(a)pyrene with maximum value of 1 ng/m3. Sixty one (61) samples from selected Metro Manila stations were analyzed. Total PAHs ranged from 1.74- 10.43 ng/m3. (author)

  2. Size distribution and probable sources of trace elements in submicron atmospheric particulate material

    International Nuclear Information System (INIS)

    Size-segregated atmospheric particulate material was collected at a rural location in the Great Smokey Mountain National Park, Tennesse, and at an urban site in Pasaden, California. The elemental composition of this material was determined by Instrumental Neutron Activation Analysis. Elements identified as being of anthropogenic origin had mass median diameters of below one micron, while elements of crustal origin were generally found to have a mass median diameters well over one micron. Some of the Pasadena samples however had elevated concentrations of the typical crustal elements Al, Fe, La, and Ce in the finer size fractions, probably due to motor vehicle emissions. (author)

  3. Atmospheric input of dissolved and particulate metals to the northwestern Mediterranean

    Science.gov (United States)

    Guieu, C.; Chester, R.; Nimmo, M.; Martin, J.-M.; Guerzoni, S.; Nicolas, E.; Mateu, J.; Keyse, S.

    Concentrations of trace elements (Al, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and Zn) were determined for aerosols, dry deposition, precipitation and total deposition samples collected from five stations on islands and in the coastal zone of the northwestern Mediterranean. Average concentrations of metals are very homogeneous over the sampled area, in particular at the three coastal sites. Cd and Pb are almost entirely of man-made origin, even in Saharan aerosols. For the other metals, the non-crustal fraction is lower in Saharan aerosols than in European aerosols, but there is an important man-made component in the Saharan aerosol, even for metals such as Fe and Cr. This confirms the results of Chester et al. (1992) who concluded that Mediterranean aerosols have a European background upon which are superimposed Saharan inputs. Dry deposition represents an important fraction of the total deposition. Partitioning of total atmospheric deposition between the dissolved and the particulate phases shows that Al, Fe and Cr originating from the atmosphere are mostly in a particulate form in the surface waters. For the other metals studied, the dissolved fraction represents more than 30% of the total input, and for Cd it is almost 100%. Extrapolation shows that more than 50% of the dissolved metals input to the northwestern Mediterranean originates from the atmosphere. Atmospheric input entirely dominates the total external input of pollution-derived elements, such as Pb and Cd. The dissolved input of atmospheric origin is also very important (> 80%) for elements of terrigeneous origin such as A1.

  4. The washout effects of rainfall on atmospheric particulate pollution in two Chinese cities.

    Science.gov (United States)

    Guo, Ling-Chuan; Zhang, Yonghui; Lin, Hualiang; Zeng, Weilin; Liu, Tao; Xiao, Jianpeng; Rutherford, Shannon; You, Jing; Ma, Wenjun

    2016-08-01

    Though rainfall is recognized as one of the main mechanisms to reduce atmospheric particulate pollution, few studies have quantified this effect, particularly the corresponding lag effect and threshold. This study aimed to investigate the association between rainfall and air quality using a distributed lag non-linear model. Daily data on ambient PM2.5 and PM2.5-10 (particulate matter with an aerodynamic diameter less than 2.5 μm and from 2.5 to 10 μm) and meteorological factors were collected in Guangzhou and Xi'an from 2013 to 2014. A better washout effect was found for PM2.5-10 than for PM2.5, and the rainfall thresholds for both particle fractions were 7 mm in Guangzhou and 1 mm in Xi'an. The decrease in PM2.5 levels following rain lasted for 3 and 6 days in Guangzhou and Xi'an, respectively. Rainfall had a better washout effect in Xi'an compared with that in Guangzhou. Findings from this study contribute to a better understanding of the washout effects of rainfall on particulate pollution, which may help to understand the category and sustainability of dust-haze and enforce anthropogenic control measures in time. PMID:27203467

  5. Temporal and spatial variabilities of atmospheric polychlorinated biphenyls (PCBs), organochlorine (OC) pesticides and polycyclic aromatic hydrocarbons (PAHs) in the Canadian Arctic: results from a decade of monitoring.

    Science.gov (United States)

    Hung, H; Blanchard, P; Halsall, C J; Bidleman, T F; Stern, G A; Fellin, P; Muir, D C G; Barrie, L A; Jantunen, L M; Helm, P A; Ma, J; Konoplev, A

    2005-04-15

    The Northern Contaminants Program (NCP) baseline monitoring project was established in 1992 to monitor for persistent organic pollutants (POPs) in Arctic air. Under this project, weekly samples of air were collected at four Canadian and two Russian arctic sites, namely Alert, Nunavut; Tagish, Yukon; Little Fox Lake, Yukon; Kinngait, Nunavut; Dunai Island, Russia and Amderma, Russia. Selected POPs, including polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and organochlorine (OC) pesticides, were analyzed in both the gas and particulate phases. This paper summarizes results obtained from this project in the past 5 years. Temporal trends were developed for atmospheric PCBs and OCs observed at Alert using a digital filtration (DF) technique. It was found that trends developed with 5 years of data (1993-1997) did not differ significantly from those determined with 7 years of data (1993-1999). This implies that with the DF technique, long-term trends can still be developed with less than 10 years of data. An acceleration in decline of OC and PCB air concentrations was noted in 1999 for some compounds, although the reason is unknown. Monitoring efforts must continue to assess the effect of this decline on the long-term trends of POPs in the Canadian Arctic. Occasional high trans-/cis-chlordane ratios and heptachlor air concentrations measured at Alert between 1995 and 1997 suggests sporadic fresh usage of chlordane-based pesticides. However, significant decreasing trends of chlordanes along with their chemical signatures has provided evidence that emission of old soil residues is replacing new usage as an important source to the atmosphere. Measurements of OC air concentrations conducted at Kinngait in 1994-1995 and 2000-2001 indicated faster OC removal at this location than at Alert. This may be attributed to the proximity of Kinngait to temperate regions where both biotic and abiotic degradation rates are faster. The PAH concentrations observed

  6. Biomass Burning: The Cycling of Gases and Particulates from the Biosphere to the Atmosphere

    Science.gov (United States)

    Levine, J. S.

    2003-12-01

    Biomass burning is both a process of geochemical cycling of gases and particulates from the biosphere to the atmosphere and a process of global change. In the preface to the book, One Earth, One Future: Our Changing Global Environment (National Academy of Sciences, 1990), Dr. Frank Press, the President of the National Academy of Sciences, writes: "Human activities are transforming the global environment, and these global changes have many faces: ozone depletion, tropical deforestation, acid deposition, and increased atmospheric concentrations of gases that trap heat and may warm the global climate."It is interesting to note that all four global change "faces" identified by Dr. Press have a common thread - they are all caused by biomass burning.Biomass burning or vegetation burning is the burning of living and dead vegetation and includes human-initiated burning and natural lightning-induced burning. The bulk of the world's biomass burning occurs in the tropics - in the tropical forests of South America and Southeast Asia and in the savannasof Africa and South America. The majority of the biomass burning, primarily in the tropics (perhaps as much as 90%), is believed to be human initiated for land clearing and land-use change. Natural fires triggered by atmospheric lightning only accounts for ˜10% of all fires (Andreae, 1991). As will be discussed, a significant amount of biomass burning occurs in the boreal forests of Russia, Canada, and Alaska.Biomass burning is a significant source of gases and particulates to the regional and global atmosphere (Crutzen et al., 1979; Seiler and Crutzen, 1980; Crutzen and Andreae, 1990; Levine et al., 1995). Its burning is truly a multidiscipline subject, encompassing the following areas: fire ecology, fire measurements, fire modeling, fire combustion, remote sensing, fire combustion gaseous and particulate emissions, the atmospheric transport of these emissions, and the chemical and climatic impacts of these emissions. Recently

  7. Use of health effect risk estimates and uncertainty in formal regulatory proceedings: a case study involving atmospheric particulates

    International Nuclear Information System (INIS)

    Coal combustion particulates are released to the atmosphere by power plants supplying electrical to the nuclear fuel cycle. This paper presents estimates of the public health risks associated with the release of these particulates at a rate associated with the annual nuclear fuel production requirements for a nuclear power plan. Utilization of these risk assessments as a new component in the formal evaluation of total risks from nuclear power plants is discussed. 23 references, 3 tables

  8. Long-range transport of continentally-derived particulate carbon in the marine atmosphere: evidence from stable carbon isotope studies

    OpenAIRE

    Cachier, Héléne; BUAT-MÉNARD, PATRICK; Fontugne, Michel; Chesselet, Roger

    2011-01-01

    Since 1979, we have investigated marine and non-marine sources of particulate carbon in the marine atmosphere from measurements of carbon concentration and isotopic composition 13C/12C). Aerosol samples were collected, mostly during the Sea/Air Exchange (SEAREX) Program experiments, in the northern and southern hemispheres (Sargasso Sea, Enewetak Atoll, Peru upwelling, American Samoa, New Zealand, Amsterdam Island). The concentration and the isotopic composition of particulate carbon of marin...

  9. Optimisation of the extraction of polycyclic aromatic hydrocarbons and their nitrated derivatives from diesel particulate matter using microwave-assisted extraction

    Energy Technology Data Exchange (ETDEWEB)

    Portet-Koltalo, F.; Oukebdane, K.; Desbene, P.L. [Universite de Rouen, Laboratoire d' Analyse des Systemes Organiques Complexes, UPRES 3233-IRCOF et IFRMP, Evreux (France); Dionnet, F. [CERTAM, Technopole du Madrillet, Saint Etienne du Rouvray (France)

    2008-01-15

    Pressurised microwave-assisted extraction was used to extract a complex mixture containing polycyclic aromatic hydrocarbons (PAHs), nitrated PAHs and heavy n-alkanes from a particularly refractory carbonaceous material resulting from the combustion in a diesel engine. A second-order central composite design was used to determine the optimal conditions of extraction in terms of time, temperature, volume and nature of extracting solvent from spiked diesel soots. To begin, methylene chloride, tetrahydrofuran and chloroform were tested for extracting the spiked diesel particulates; however, the nature of these solvents was not really an influential factor. Volume was the most influential factor and was kept at a medium level to enhance the extraction of heavy PAHs without introducing an important dilution factor. Temperature and time were not influential as main factors but interacted with the other factors. Finally, high temperature and duration associated with a medium volume of methylene chloride were better for the extractions. After this optimisation, five-ring and six-ring PAHs were nevertheless not satisfactorily desorbed. Other solvents were therefore tested. Only aromatic ones, and particularly heterocyclic aromatic solvents, managed to desorb the heaviest PAHs. Pyridine, with its both aromatic and its basic character, was the most successful solvent. Desorption was even complete with an addition of 17% of diethylamine into pyridine. So, using MAE, we succeeded in extracting quantitatively, from the spiked refractory diesel soot surface, two-ring to six-ring PAHs, heavy n-alkanes and short nitrated PAHs. However, heavy nitrated PAHs were better extracted with a small addition of acetic acid (1%) into pyridine instead of a basic cosolvent. (orig.)

  10. Determination of 43 polycyclic aromatic hydrocarbons in air particulate matter by use of direct elution and isotope dilution gas chromatography/mass spectrometry.

    Science.gov (United States)

    Li, Zheng; Pittman, Erin N; Trinidad, Debra A; Romanoff, Lovisa C; Mulholland, James; Sjödin, Andreas

    2010-02-01

    We are reporting a method for measuring 43 polycyclic aromatic hydrocarbons (PAH) and their methylated derivatives (Me-PAHs) in air particulate matter (PM) samples using isotope dilution gas chromatography/high-resolution mass spectrometry (GC/HRMS). In this method, PM samples were spiked with internal standards, loaded into solid phase extraction cartridges, and eluted by dichloromethane. The extracts were concentrated, spiked with a recovery standard, and analyzed by GC/HRMS at 10,000 resolution. Sixteen (13)C-labeled PAHs and two deuterated Me-PAHs were used as internal standards to account for instrument variability and losses during sample preparation. Recovery of labeled internal standards was in the range of 86-115%. The proposed method is less time-consuming than commonly used extraction methods, such as sonication and accelerated solvent extraction (ASE), and it eliminates the need for a filtration step required after the sonication extraction method. Limits of detection ranged from 41 to 332 pg/sample for the 43 analytes. This method was used to analyze reference materials from the National Institute of Standards and Technology. The results were consistent with those from ASE and sonication extraction, and these results were also in good agreement with the certified or reference concentrations. The proposed method was then used to measure PAHs on PM(2.5) samples collected at three sites (urban, suburban, and rural) in Atlanta, GA. The results showed distinct seasonal and spatial variation and were consistent with an earlier study measuring PM(2.5) samples using an ASE method, further demonstrating the compatibility of this method and the commonly used ASE method. PMID:19936717

  11. Distribution and ecological risk assessment of polycyclic aromatic hydrocarbons in water, suspended particulate matter and sediment from Daliao River estuary and the adjacent area, China.

    Science.gov (United States)

    Zheng, Binghui; Wang, Liping; Lei, Kun; Nan, Bingxu

    2016-04-01

    Polycyclic aromatic hydrocarbons (PAHs) contamination was investigated in concurrently sampled surface water, suspended particulate matter (SPM) and sediment of Daliao River estuary and the adjacent area, China. The total concentrations of PAHs ranged from 71.12 to 4255.43 ng/L in water, from 1969.95 to 11612.21 ng/L in SPM, and from 374.84 to 11588.85 ng/g dry weight (dw) in sediment. Although the 2-3 ring PAHs were main PAH congeners in water and SPM, the 4-6 ring PAHs were also detected and their distribution was site-specific, indicating a very recent PAHs input around the area since they were hydrophobic. The PAHs pollution was identified as mixed combustion and petroleum sources. Based on species sensitivity distribution (SSD), the ecological risk in SPM from 82% stations was found to be higher obviously than that in water. The risk in water was basically ranked as medium, while the risk in SPM was ranked as high. Analysis with sediment quality guidelines (SQGs) indicated that negative eco-risk occasionally occurred in about 50% stations, while negative eco-risk frequently occurred in about 3% stations only caused by Phenanthrene(Phe) and Dibenzo(a,h)anthracene(DBA). Here freshwater acute effects data together with saltwater data were used for SSD model. And this method could quickly give the rational risk information, and achieved our objective that compared the spatial difference of risk levels among three compartments. The results confirmed that the use of freshwater acute effects data from the ECOTOX database together with saltwater effects data is acceptable for risk assessment purposes in estuary. PMID:26855211

  12. The Influence of Sandstorms and Long-Range Transport on Polycyclic Aromatic Hydrocarbons (PAHs) in PM2.5 in the High-Altitude Atmosphere of Southern China

    OpenAIRE

    Minmin Yang; Yan Wang; Qiang Liu; Aijun Ding; Yuhua Li

    2015-01-01

    PM2.5 (Particulate Matter 2.5) samples were collected at Mount Heng and analyzed for polycyclic aromatic hydrocarbons (PAHs). During sampling, a sandstorm from northern China struck Mount Heng and resulted in a mean PM2.5 concentration of 150.61 μg/m3, which greatly exceeded the concentration measured under normal conditions (no sandstorm: 58.50 μg/m3). The average mass of PAHs in PM2.5 was 30.70 μg/g, which was much lower than in the non-sandstorm samples (80.80 μg/g). Therefore, the sandsto...

  13. 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 sampling was carried out on quartz fibre filters. Based on meteorological conditions and PM mass concentrations, each one of the 7 groups of filters collected during the first week were combined with the corresponding filters of the third week. The same procedure was undertaken with samples of the second and fourth weeks. Filters of 0.95-0.45 and samples were subjected to organic analysis by gas chromatography-mass spectrometry (GC-MS), after solvent extraction of filters and an appropriate derivatisation technique. Besides the homologous compound series of organic classes (e.g. n-alkanes, n-alkanols and n-alkanoic acids), special attention was given to the determination of specific molecular markers for different sources (e.g. vehicular). Carbon preference indices (CPI) close to the unity and the presence of

  14. Mass Fraction Spatiotemporal Geostatistics and its Application to Map Atmospheric Polycyclic Aromatic Hydrocarbons after 9/11

    Science.gov (United States)

    Extensive research has been conducted on effects resulting from exposure to ambient particulate matter. Particulate matter has been linked to cardiovascular diseases, respiratory problems, and reproductive effects. A large body of work on particulate matter focuses on atmospher...

  15. Inhalation and dermal exposure to atmospheric polycyclic aromatic hydrocarbons and associated carcinogenic risks in a relatively small city.

    Science.gov (United States)

    Gungormus, Elif; Tuncel, Semra; Hakan Tecer, Lokman; Sofuoglu, Sait C

    2014-10-01

    The aim of this study was to conduct a carcinogenic risk assessment for exposure to polycyclic aromatic hydrocarbons (PAHs) via routes of inhalation and dermal contact. Concentrations of 19 PAH species were determined during a heating period at a site in the city of Balikesir, Turkey. Two questionnaires were administered to a sample of inhabitants to determine time-activity budgets and demographic information. The assessment was conducted for each participant and Balikesir population by deterministic and probabilistic approaches, respectively. Monte Carlo simulation was implemented to determine the population exposure-risk probability distributions. The estimates were based on benzo[a]pyrene equivalent (BaPeq) total PAH concentrations calculated using toxic equivalency factors. The mean and median BaPeq concentrations of gaseous and particulate phases were 3.25 and 1.34, and 38.5 and 34.0ng/m(3), respectively. Carcinogenic risk for inhalation exposure route was estimated by using two different slope factor values (3.9 and 304.5(mg/kg-day)(-1)), recommended by two different organizations, resulting in two (order(s) of magnitude apart) population risk ranges: 1.32×10(-7)-2.23×10(-4), and 1.61×10(-5)-7.95×10(-3), respectively. The population risks associated with dermal exposure were lower compared to those of inhalation, ranging from 6.58×10(-9) to 2.57×10(-6). The proportion of the population with risks higher than the general acceptable level (1.0×10(-6)) was estimated as >99 percent, for inhalation, and as 28 percent for dermal exposure route. PMID:25046852

  16. Seasonal variations in the concentration and solubility of elements in atmospheric particulate matter: a case study in Northern Italy

    Directory of Open Access Journals (Sweden)

    Canepari S.

    2013-04-01

    Full Text Available Atmospheric particulate matter is characterized by a variety of chemical components, generally produced by different sources. Chemical fractionation of elements, namely the determination of their extractable and residual fractions, may reliably increase the selectivity of some elements as tracers of specific PM sources. Seasonal variations of atmospheric particulate matter concentration in PM10 and PM2.5, of elemental concentration in PM10 and PM2.5, of the extractable and residual fraction of elements in different size fractions in the range 0.18 – 18 μm are reported in this paper. The effect of the ageing of the air masses is discussed.

  17. Development of methods for the speciation of metals in atmospheric particulate matter

    Science.gov (United States)

    Majestic, Brian J.

    2007-12-01

    This study focuses on advancing methods to measure and speciate trace-elements in atmospheric particulate matter (PM) to support human exposure and health studies. Methods were developed to measure Fe(II) and Fe(III) in PM samples using samplers collecting daily average particulate matter samples and personal exposure samples. Low-cost wet-chemical methods were also developed to measure the oxidation state of leachable iron, chromium and manganese present in low-volume PM samples. In addition, a study was conducted to determine if metals collected by different personal exposure samplers currently used in exposure and health studies were comparable. Results from the intercomparison study between co-located personal and fixed-site ambient samplers showed that different personal sampler designs display biases that are largest for metals predominating in the super-micron fraction. Using one consistent personal exposure sampler, a pilot study was conducted to examine trace-metal concentrations in personal exposure samples from individuals residing in an assisted-living home. These results were compared to ambient outdoor and fixed-indoor concentrations, and generally, outdoor > indoor > personal exposure concentrations. The pilot study demonstrated that adequate tools exist to measure trace-element exposures under real-world conditions. Using the methods developed in the study, labile Fe(II) and Fe(III) as well as total soluble manganese and soluble oxidized manganese from atmospheric PM were routinely detected in ambient and personal exposure samples. Samples extracted in a variety of environmentally and biologically relevant fluids showed that leachable iron and manganese strongly depends on the extractant. Atmospheric samples from a residential location in Toronto (which uses the fuel additive, MMT) showed that a significant fraction of oxidized labile manganese is present in the PM2.5 fraction, in contrast to US cities that do not use MMT. Both the wet-chemical and

  18. Assessment of Elemental Content in Airborne Particulate Matter in Bratislava Atmosphere using INAA and AAS

    Science.gov (United States)

    Meresova, J.; Florek, M.; Frontasyeva, M. V.; Pavlov, S. S.; Holy, K.; Sykora, I.

    2007-11-01

    The wide range concentration of elements including heavy metals, halogens and rare earths in airborne particulate matter were investigated. Sixteen samples were collected on filters in Meteorological station, Comenius University Bratislava (Slovak Republic) in different seasons. Using instrumental neutron activation analysis (INAA) the concentrations of 29 elements (Na, Al, Cl, K, Ca, Sc, Ti, V, Mn, Fe, Ga, As, Se, Br, Rb, In, Sb, I, Cs, Ba, La, Sm, Dy, Tm, W, Au, Hg, Th, U) were determined. The concentrations of other 6 elements (Cr, Ni, Cu, Zn, Cd, Pb) were measured by atomic absorption spectrometry (AAS). The obtained results allow us to better understand the dynamic processes in the atmosphere and to quantify the air pollution and its trends.

  19. The role of neutron activation analysis for trace elements characterization, analysis and certification in atmospheric particulates

    International Nuclear Information System (INIS)

    The Neutron Activation Analysis (NAA) owns these requirements and is universally accepted as one of the most reliable analytical tools for trace and ultratrace elements determination. Its use in trace elements atmospheric pollution related studies has been and is still extensive as can be demonstrate by several specific works and detailed reviews. In this work, the application of this nuclear technique, in solving a series of different analytical problems related to trace elements in air pollution processes is reported. Examples and results are given on the following topics: characterization of urban and rural airborne particulate samples; particles size distribution in the different inhalable and respirable fractions (PM10 and PM 2.5); certification of related Standard Reference Materials for data quality assurance. (author)

  20. Diurnal and nocturnal measurements of PAH, nitro-PAH, and oxy-PAH compounds in atmospheric particulate matter of a sugar cane burning region

    Science.gov (United States)

    Souza, Kely F.; Carvalho, Lilian R. F.; Allen, Andrew G.; Cardoso, Arnaldo A.

    2014-02-01

    Polycyclic aromatic hydrocarbons (PAHs), nitro-PAHs, and oxy-PAHs were studied in the atmospheric particulate matter of a subtropical rural region (São Paulo State, Brazil) affected by emissions from sugar cane burning. Diurnal and nocturnal samples were collected from May to June of 2010. In general, average PAH concentrations were significantly higher at night, suggesting that the compounds were predominantly emitted to the atmosphere during biomass burning (which was mainly performed at night). The maximum average PAH concentration was found for benzo[b]fluoranthene at night (2.9 ± 5.4 ng m-3). Among the nitro-PAH compounds, the highest average concentrations were obtained for 9-nitrophenanthrene in diurnal and nocturnal samples (1.5 ± 1.2 and 1.3 ± 2.1 ng m-3, respectively). In contrast to the PAH and nitro-PAH compounds, the oxy-PAHs could not be directly associated with sugar cane burning. The most abundant oxy-PAH compound was benzanthrone (1.6 ± 1.3 ng m-3) at night, followed by 9,10-anthraquinone (1.1 ± 0.9 ng m-3) and 9-fluorenone (0.4 ± 0.1 ng m-3) during the day. A correlation matrix was used to explore the origins of the different compounds. The data suggested that during the daytime, direct emissions (mainly in vehicle exhaust) contributed to the presence of PAHs, nitro-PAHs, and oxy-PAHs in air. Photochemical production also appeared to be a source of the majority of nitro-PAHs and oxy-PAHs, while photolysis could have contributed to removal of the nitro-PAHs during the daytime. At night, sugar cane burning emissions were the primary source of the PAHs and nitro-PAHs, with additional sources also contributing to the levels of oxy-PAHs in the atmosphere.

  1. Mutagenicity profile of atmospheric particulate matter in a small urban center subjected to airborne emission from vehicle traffic and sugar cane burning.

    Science.gov (United States)

    Alves, Debora Kristina M; Kummrow, Fábio; Cardoso, Arnaldo A; Morales, Daniel A; Umbuzeiro, Gisela A

    2016-01-01

    Atmospheric particulate matter (PM) is genotoxic and recently was classified as carcinogenic to humans by the International Agency for Research on Cancer. PM chemical composition varies depending on source and atmospheric conditions. The Salmonella/microsome assay is the most used mutagenicity test and can identify the major chemical classes responsible for observed mutagenicity. The objective of this work was to characterize the mutagenicity of PM samples from a countryside city, Limeira, Brazil, which is influenced by heavy traffic and sugar cane biomass burning. Six samples of total PM were collected. Air mass backward trajectories were calculated. Organic extracts were assayed using the Salmonella/microsome microsuspension mutagenicity assay using TA98, YG1041, and TA1538, with and without metabolic activation (S9). YG1041 was the most sensitive strain and mutagenicity reached 9,700 revertants per m(3) without metabolic activation. Potency for TA1538 was higher than TA98, indicating that this strain should be considered in air mutagenicity studies. The increased response to YG1041 relative to TA98, and the decreased response with S9, suggests that nitroaromatics are the major contributors. Limeira is among the most mutagenic cities in the world. High mutagenicity in Limeira seems to occur when the air mass from the area of sugarcane production is mixed with air from the region impacted by anthropogenic activities such as traffic. An increase in the formation of nitro-polycyclic aromatic hydrocarbons may result from longer contact time between the aromatic compounds and the atmosphere with high NOx and ozone concentration, although more studies are required to confirm this hypothesis. PMID:26289646

  2. 40 CFR Appendix O to Part 50 - Reference Method for the Determination of Coarse Particulate Matter as PM10-2.5 in the Atmosphere

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 2 2010-07-01 2010-07-01 false Reference Method for the Determination of Coarse Particulate Matter as PM10-2.5 in the Atmosphere O Appendix O to Part 50 Protection of... Coarse Particulate Matter as PM10-2.5 in the Atmosphere 1.0Applicability and Definition 1.1This...

  3. 40 CFR Appendix L to Part 50 - Reference Method for the Determination of Fine Particulate Matter as PM2.5 in the Atmosphere

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 2 2010-07-01 2010-07-01 false Reference Method for the Determination of Fine Particulate Matter as PM2.5 in the Atmosphere L Appendix L to Part 50 Protection of... Fine Particulate Matter as PM2.5 in the Atmosphere 1.0 Applicability. 1.1This method provides for...

  4. A bacterial bioreporter panel to assay the cytotoxicity of atmospheric particulate matter

    Science.gov (United States)

    Kessler, Nivi; Schauer, James J.; Yagur-Kroll, Sharon; Melamed, Sahar; Tirosh, Ofir; Belkin, Shimshon; Erel, Yigal

    2012-12-01

    Numerous studies have demonstrated that elevated concentrations of suspended atmospheric particulate matter (PM) are associated with adverse health effects. In order to minimize the adverse public health effects of atmospheric PM by exposure management, there is a need for a greater understanding of the toxic mechanisms and the components that are responsible for the toxic effects. The aim of this study was to utilize bioassay techniques to investigate these aspects. For this purpose a reporter panel of 9 genetically engineered bacterial (Escherichia coli) strains was composed. Each panel member was designed to report on a different stress condition with a measurable light signal produced by the luciferase enzyme. Toxic mechanisms and components were studied using six anthropogenic PM source samples, including two vehicle combustion particles, three coal fly ash (CFA) samples and an urban dust sample. The most prominent outcome of the panel exposure results were broad panel responses observed for two of the CFA samples, indicating oxidative stress, respiration inhibition and iron deficiency. These responses were relieved when the samples were treated with EDTA, a non-specific metal chelator, suggesting the involvement of metals in the observed effects. Bioavailability analysis of the samples suggests that chromium was related to the toxic responses induced by two of the CFA samples. Oxidative stress was also observed in several samples of ambient atmospheric aerosols and excess metal toxicity in an urban dust sample collected in a parking lot. The reporter panel approach, as demonstrated in this study, has the potential of providing novel insights as to the mechanisms of atmospheric PM toxicity. Furthermore, combining the panel's results with bioavailability data can enlighten about the role of different PM components in the observed toxicity.

  5. Size and time-resolved roadside enrichment of atmospheric particulate pollutants

    Directory of Open Access Journals (Sweden)

    F. Amato

    2011-01-01

    Full Text Available Size and time-resolved roadside enrichments of atmospheric particulate pollutants in PM10 were detected and quantified in a Mediterranean urban environment (Barcelona, Spain. Simultaneous data from one urban background (UB, one traffic (T and one heavy traffic (HT location were analysed, and roadside PM10 enrichments (RE in a number of elements arising from vehicular emissions were calculated. Tracers of primary traffic emissions (EC, Fe, Ba, Cu, Sb, Cr, Sn showed the largest REs (>70%. Other traffic tracers (Zr, Cd showed lower but still consistent REs (25–40%, similar to those obtained for mineral matter resulting from road dust resuspension (Ca, La, Ce, Ti, Ga, Sr, 30–40%. The sum of primary and secondary organic carbon showed a RE of 41%, with contributions of secondary OC (SOC to total OC ranging from 46% at the HT site, 63% at the T site, and 78% in the UB. Finally, other trace elements (As, Co, Bi showed unexpected but consistent roadside enrichments (23% up to 69%, suggesting a link to traffic emissions even though the emission process is unclear.

    Hourly-resolved PM speciation data proved to be a highly resourceful tool to determine the source origin of atmospheric pollutants in urban environments. At the HT site, up to 62% of fine Mn was attributable to industrial plumes, whereas coarse Mn levels were mainly attributed to traffic. Similarly, even though Zn showed on average no roadside enrichment and thus was classified as industrial, the hourly-resolved data proved that at least 15% of coarse Zn may be attributed to road traffic emissions. In addition, our results indicate that secondary nitrate formation occurs within the city-scale, even in the absence of long atmospheric residence times or long-range atmospheric transport processes.

  6. Real-time measurements of particulate matter and polycyclic aromatic hydrocarbon emissions from stationary combustion sources used in oil and gas production

    International Nuclear Information System (INIS)

    Particulate matter emissions and some components of the particles were measured in the exhaust from combustion equipment used in oil and gas production operations near Bakersfield, California. The combustion sources included a 22.5 MW (electric) turbine generator, a 342-Bhp rich-burn spark ignition engine, and a 50 million Btu/h steam generator, all fired using natural gas. The particle components and measurement techniques were as follows: (1) Calcium, magnesium, sodium, silicon, and iron were measured using laser-induced breakdown spectroscopy (LIBS), (2) particle-bound polycyclic aromatic hydrocarbons (PAH) were detected using the charge produced by photoionization, (3) particles having sizes between 0.1 and 7.5 (micro)m were counted using an instrument based on light scattering, and (4) total particulate matter was measured according to US EPA Method 5. Not all of the methods were applied to all of the sources. Measurements were also made in the ambient air near the combustion air inlets to the units, for comparison with the concentrations in the exhaust, but the inlet and outlet measurements were not done simultaneously. Calcium, sodium, and silicon were found in the exhaust from the steam generator at concentrations similar to those in the ambient air near the inlet to the burner. Sodium and silicon were observed in the engine exhaust at levels a factor of four higher than their concentrations in the air. The principal metal observed in the engine exhaust was calcium, a component of the lubricating oil, at a concentration of 11.6 (micro)g/m3. The air entering the gas turbine is filtered, so the average concentrations of metals in the turbine exhaust under steady operating conditions were even lower than in the air. During start-up following a shut-down to wash the turbine, silicon and iron were the major species in the stack, at concentrations of 6.4 and 16.2 (micro)g/m3, respectively. A possible source of silicon is the water injected into the turbine for

  7. Eco-physiological Effects of Atmospheric Ozone and Polycyclic Aromatic Hydrocarbons (PAHs) on Plants

    Science.gov (United States)

    Bandai, S.; Sakugawa, H. H.

    2012-12-01

    [Introduction] Tropospheric ozone is one of most concerned air pollutant, by causing damage to trees and crops. Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous contaminants found in various environmental compartments. Photo-induced toxicity of PAHs can be driven from formation of intracellular single oxygen and other reactive oxygen intermediates (ROI) leading to biological damages.(1) In the present study, we measured photosynthesis rate and other variables to investigate the effects of ozone and PAHs on the eco-physiological status of plants such as eggplant, common bean and strawberry. Plants treated with the single or combined air pollutants are expected to exhibit altered physiological, morphological and possibly growth changes. [Materials and Methods] We performed three exposure experiments. Exp.1. Eggplant (Solanum melongena) seedlings, were placed in the open-top chambers (n=6 plants/treatment). Treatment system was ozone (O)(120ppb), phenanthrene (P)(10μM), O+P, fluoranthene (F)(10μM), O+F, mannitol (M)(1mM) and the control (Milli-Q water)(C). P, F and M were sprayed three times weekly on the foliage part of eggplant. Average volume sprayed per seedling was 50mL. The treatment period was 30days and [AOT 40 (Accumulated exposure over a threshold of 40 ppb)]=28.8 ppmh. Exp.2, Common bean (Phaseolus vulgaris L.) seedlings were used (n=5 plants/treatment). The treatment system was the same as Exp.1. The treatment period was 40days and [AOT 40]=38.4ppmh. Exp.3. Strawberry (Fragaria L.) seedlings were used (n=5 plants/treatment). Treatment system was O (120ppb), F(10μM), O+F, F+M, O+M and C. The treatment period was 90days and [AOT 40]=86.4ppmh. Ecophysiological variables examined were photosynthesis rate measured at saturated irradiance (Amax), stomatal conductance to water vapour (gs), internal CO2 concentration (Ci), photochemical efficiency of PS2 in the dark (Fv/Fm), chlorophyll contents, visual symptom assessment and elemental composition in the

  8. Behavior of Particulate Mercury in the Bulk Atmospheric Aerosols Simultaneously Collected at 2 Sites in Okinawa, Japan

    Science.gov (United States)

    Miyagi, Y.; Arakaki, T.; Azechi, S.; Somada, Y.; Oshiro, Y.; Tsuhako, A.; Murayama, H.; Tanahara, A.

    2013-12-01

    Mercury is toxic to animals. Mercury is emitted to the atmosphere mainly from two sources; natural and anthropogenic sources. Natural sources include volcanic eruption, forest fire and so on. Anthropogenic sources include fossil fuel combustion, metal and cement production and so on. There are three forms of mercury in the atmosphere: gaseous elemental mercury, reactive gaseous mercury and particulate mercury. Gaseous elemental mercury is the most abundant form in the atmosphere, and has long atmospheric lifetime, ca. a few years. This study focuses on particulate mercury, which has a relatively short lifetime, ca. a few days, in the atmosphere because it reflects characteristics of nearby emission sources. Objectives of this study were to elucidate the behavior of particulate mercury in aerosols and to understand relationships between mercury and other metals and water-soluble anions. Aerosol samples were collected at two sites; Cape Hedo Atmosphere and Aerosol Monitoring Station (CHAAMS, Jan.2008-Nov.2012), northern tip of Okinawa island, and University of the Ryukyus (UR, Jan.2008-Nov.2012), central and more populated area of Okinawa island. They were collected by using identical high-volume air samplers on quartz filters. Concentrations of particulate mercury in aerosols were determined by using a MA-3000 (Nippon Instruments Corporation). The results showed that particulate Hg concentrations were mostly higher for the aerosols collected at UR site than those at CHAAMS site, suggesting locally emitted Hg. Samples collected at UR showed clear seasonal variation, the lowest in summer and the highest winter. On the other hand, the CHAAMS samples showed lower concentration in winter and higher concentration in summer, but the difference was relatively small. Both UR and CHAAMS samples had similar concentration levels in summer season. Back trajectory analysis showed that particulate Hg at CHAAMS site during summer was not from Asian continent. Since samples

  9. Atmospheric particulate mercury in the megacity Beijing: Efficiency of mitigation measures and assessment of health effects

    Science.gov (United States)

    Schleicher, N. J.; Schäfer, J.; Chen, Y.; Blanc, G.; Chen, Y.; Chai, F.; Cen, K.; Norra, S.

    2016-01-01

    Atmospheric particulate mercury (HgP) was studied before, during, and after the Olympic Summer Games in Beijing, China, in August 2008 in order to investigate the efficiency of the emission control measures implemented by the Chinese Government. These source control measures comprised traffic reductions, increase in public transportation, planting of vegetation, establishment of parks, building freeze at construction sites, cleaner production techniques for industries and industry closures in Beijing and also in the surrounding areas. Strictest measures including the "odd-even ban" to halve the vehicle volume were enforced from the 20th of July to the 20th of September 2008. The Olympic period provided the unique opportunity to investigate the efficiency of these comprehensive actions implemented in order to reduce air pollution on a large scale. Therefore, the sampling period covered summer (August, September) and winter (December and January) samples over several years from December 2005 to September 2013. Average HgP concentrations in total suspended particulates (TSP) sampled in August 2008 were 81 ± 39 pg/m3 while TSP mass concentrations were 93 ± 49 μg/m3. This equals a reduction by about 63% for TSP mass and 65% for HgP, respectively, compared to the previous two years demonstrating the short-term success of the measures. However, after the Olympic Games, HgP concentrations increased again to pre-Olympic levels in August 2009 while values in August 2010 decreased again by 30%. Moreover, winter samples, which were 2- to 11-fold higher than corresponding August values, showed decreasing concentrations over the years indicating a long-term improvement of HgP pollution in Beijing. However, regarding adverse health effects, comparisons with soil guideline values and studies from other cities highlighted that HgP concentrations in TSP remained high in Beijing despite respective control measures. Consequently, future mitigation measures need to be tailored more

  10. Suspended Particulates Concentration (PM10 under Unstable Atmospheric Conditions over Subtropical Urban Area (Qena, Egypt

    Directory of Open Access Journals (Sweden)

    M. El-Nouby Adam

    2013-01-01

    Full Text Available The main purpose of this study is to evaluate the suspended particulates (PM10 in the atmosphere under unstable atmospheric conditions. The variation of PM10 was investigated and primary statistics were employed. The results show that, the PM10 concentrations values ranged from 6.00 to 646.74 μg m−3. The average value of PM10 is equal to 114.32 μg m−3. The high values were recorded in April and May (155.17 μg m−3 and 171.82 μg m−3, respectively and the low values were noted in February and December (73.86 μg m−3 and 74.05 μg m−3, respectively. The average value of PM10 of the hot season (125.35 × 10−6 g m−3 was higher than its value for the cold season (89.27 μg m−3. In addition, the effect of weather elements (air temperature, humidity and wind on the concentration of PM10 was determined. The multiple R between PM10 and these elements ranged from 0.05 to 0.47 and its value increased to reach 0.73 for the monthly average of the database used. Finally, the PM10 concentrations were grouped depending on their associated atmospheric stability class. These average values were equal to 122.80 ± 9 μg m−3 (highly unstable or convective, 109.37 ± 12 μg m−3 (moderately unstable and 104.42 ± 15 μg m−3 (slightly unstable.

  11. Atmospheric versus biological sources of polycyclic aromatic hydrocarbons (PAHs) in a tropical rain forest environment

    International Nuclear Information System (INIS)

    To distinguish between pyrogenic and biological sources of PAHs in a tropical rain forest near Manaus, Brazil, we determined the concentrations of 21 PAHs in leaves, bark, twigs, and stem wood of forest trees, dead wood, mineral topsoil, litter layer, air, and Nasutitermes termite nest compartments. Naphthalene (NAPH) was the most abundant PAH with concentrations of 35 ng m-3 in air (>85% of the Σ21PAHs concentration), up to 1000 μg kg-1 in plants (>90%), 477 μg kg-1 in litter (>90%), 32 μg kg-1 in topsoil (>90%), and 160 μg kg-1 (>55%) in termite nests. In plants, the concentrations of PAHs in general decreased in the order leaves > bark > twigs > stem wood. The concentrations of most low-molecular weight PAHs in leaves and bark were near equilibrium with air, but those of NAPH were up to 50 times higher. Thus, the atmosphere seemed to be the major source of all PAHs in plants except for NAPH. Additionally, phenanthrene (PHEN) had elevated concentrations in bark and twigs of Vismia cayennensis trees (12-60 μg kg-1), which might have produced PHEN. In the mineral soil, perylene (PERY) was more abundant than in the litter layer, probably because of in situ biological production. Nasutitermes nests had the highest concentrations of most PAHs in exterior compartments (on average 8 and 15 μg kg-1 compared to -1 in interior parts) and high PERY concentrations in all compartments (12-86 μg kg-1), indicating an in situ production of PERY in the nests. Our results demonstrate that the deposition of pyrolytic PAHs from the atmosphere controls the concentrations of most PAHs. However, the occurrence of NAPH, PHEN, and PERY in plants, termite nests, and soils at elevated concentrations supports the assumption of their biological origin. - Evidence of non-pyrolytic, biogenic production of PAHs is provided

  12. Estimating the influence of different urban canopy cover types on atmospheric particulate matter (PM10) pollution abatement in London UK

    OpenAIRE

    Tallis, Matthew J.

    2010-01-01

    In the urban environment atmospheric pollution by PM10 (particulate matter with a diameter less than 10 x 10-6 m) is a problem that can have adverse effects on human health, particularly increasing rates of respiratory disease. The main contributors to atmospheric PM10 in the urban environment are road traffic, industry and power production. The urban tree canopy is a receptor for removing PM10s from the atmosphere due to the large surface areas generated by leaves and air turbulence creat...

  13. Relationship between atmospheric pollution in the residential area and concentrations of polycyclic aromatic hydrocarbons (PAHs) in human breast milk.

    Science.gov (United States)

    Pulkrabova, Jana; Stupak, Michal; Svarcova, Andrea; Rossner, Pavel; Rossnerova, Andrea; Ambroz, Antonin; Sram, Radim; Hajslova, Jana

    2016-08-15

    Human milk is an important source of beneficial nutrients and antibodies for newborns and infants and, under certain circumstances, its analysis may provide information on mothers' and infants' exposure to various contaminants. In the presented study, we have introduced the new analytical approach for analysis of 24 highly occurring polycyclic aromatic hydrocarbons (PAHs) in this indicator matrix. The sample preparation procedure is based on an ethyl acetate extraction of milk; the transfer of analytes into an organic layer is enhanced by addition of inorganic salts, i.e. sodium chloride and magnesium sulphate. Following the clean-up of a crude extract on silica SPE columns, gas chromatography coupled to triple quadrupole mass spectrometry is used for PAH identification and quantitation. The average recoveries of targeted PAHs from spiked samples were in the range of 68-110% with repeatabilities below 30% and method quantitation limits ranging from 0.03 to 0.3ng/g lipid weight. This newly validated method was successfully applied for analyses of 324 human milk samples collected from nonsmoking women during two sampling periods (summer and winter) in two residential areas in the Czech Republic differing in atmospheric pollution by PAHs. From 24 targeted analytes 17 were detected at least in one sample. Phenantherene, fluoranthrene, pyrene and fluorene were the most abundant compounds found at average concentration of 13.81, 1.80, 0.86, and 2.01ng/g lipid weight respectively. Comparing the data from two sampling periods, in both areas higher concentrations were measured in samples collected during winter. Also in the highly industrialized locality with heavily contaminated air PAH amounts in milk were higher than in the control locality. These first data on PAH concentrations in human milk collected in the Czech Republic are comparable with measurements for nonsmoking women reported earlier in the United States but significantly lower than results from China, Turkey

  14. Size and time-resolved roadside enrichment of atmospheric particulate pollutants

    Directory of Open Access Journals (Sweden)

    F. Amato

    2011-03-01

    Full Text Available Size and time-resolved roadside enrichments of atmospheric particulate pollutants in PM10 were detected and quantified in a Mediterranean urban environment (Barcelona, Spain. Simultaneous data from one urban background (UB, one traffic (T and one heavy traffic (HT location were analysed, and roadside PM10 enrichments (RE in a number of elements arising from vehicular emissions were calculated. Tracers of primary traffic emissions (EC, Fe, Ba, Cu, Sb, Cr, Sn showed the largest REs (>70%. Other traffic tracers (Zr, Cd showed lower but still consistent REs (25–40%, similar to those obtained for mineral matter resulting from road dust resuspension (Ca, La, Ce, Ti, Ga, Sr, 30–40%. The sum of primary and secondary organic carbon showed a RE of 41%, with contributions of secondary OC (SOC to total OC ranging from 46% at the HT site, 63% at the T site, and 78% in the UB. Finally, other trace elements (As, Co, Bi showed unexpected but consistent roadside enrichments (23% up to 69%, suggesting a link to traffic emissions even though the emission process is unclear.

    Hourly-resolved PM speciation data proved to be a highly resourceful tool to determine the source origin of atmospheric pollutants in urban environments. At the HT site, up to 62% of fine Mn was attributable to industrial plumes, whereas coarse Mn levels were mainly attributed to traffic. Similarly, even though Zn showed on average no roadside enrichment and thus was classified as industrial, the hourly-resolved data proved that at least 15% of coarse Zn may be attributed to road traffic emissions. In addition, our results indicate that secondary nitrate formation occurs within the city-scale, even in the absence of long atmospheric residence times or long-range atmospheric transport processes. Characteristic tracer ratios of road traffic emissions were identified: Cu/Sb = 6.8–8.0, Cu/Sn = 4.7–5.4 and Sn/Sb = 1.5.

  15. Seasonal variations and source estimation of saccharides in atmospheric particulate matter in Beijing, China.

    Science.gov (United States)

    Liang, Linlin; Engling, Guenter; Du, Zhenyu; Cheng, Yuan; Duan, Fengkui; Liu, Xuyan; He, Kebin

    2016-05-01

    Saccharides are important constituents of atmospheric particulate matter (PM). In order to better understand the sources and seasonal variations of saccharides in aerosols in Beijing, China, saccharide composition was measured in ambient PM samples collected at an urban site in Beijing. The highest concentrations of total saccharides in Beijing were observed in autumn, while an episode with abnormal high total saccharide levels was observed from 15 to 23 June, 2011, due to extensive agricultural residue burning in northern China during the wheat harvest season. Compared to the other two categories of saccharides, sugars and sugar alcohols, anhydrosugars were the predominant saccharide group, indicating that biomass burning contributions to Beijing urban aerosol were significant. Ambient sugar and sugar alcohol levels in summer and autumn were higher than those in spring and winter, while they were more abundant in PM2.5 during winter time. Levoglucosan was the most abundant saccharide compound in both PM2.5 and PM10, the annual contributions of which to total measured saccharides in PM2.5 and PM10 were 61.5% and 54.1%, respectively. To further investigate the sources of the saccharides in ambient aerosols in Beijing, the PM10 datasets were subjected to positive matrix factorization (PMF) analysis. Based on the objective function to be minimized and the interpretable factors identified by PMF, six factors appeared to be optimal as to the probable origin of saccharides in the atmosphere in Beijing, including biomass burning, soil or dust, isoprene SOA and the direct release of airborne fungal spores and pollen. PMID:26921589

  16. Change characteristic of atmospheric particulate mercury during dust weather of spring in Qingdao, China

    Science.gov (United States)

    Zhang, Yuqing; Liu, Ruhai; Wang, Yan; Cui, Xueqing; Qi, Jianhua

    2015-02-01

    Atmospheric aerosol samples were collected during dust weather of spring from 2008 to 2011 in Qingdao, in which the concentrations of atmospheric particulate mercury (PHg) were measured to analyze its distribution characteristics and source. PHg concentration during the study ranged from 0.050 ng m-3 to 0.788 ng m-3 with the average 0.292 ng m-3 in dust day, while 0.085 ng m-3 to 0.444 ng m-3 with the average 0.188 ng m-3 in non-dust day. PHg concentration in dust day is far higher than that in some cities of South Korea and Japan and comparable to some cities in China. There was a statistically power function between PHg/TSP and TSP concentrations, which meant that intense dust (high TSP) brought particles with low mercury content. The estimated dry deposition flux of PHg is 0.9-14.2 ng m-2 h-1 with the mean 5.26 ng m-2 h-1 in dust day. The mercury deposition flux in a dust day accounts for almost 1% annual flux, which should be paid attention in the regional and global cycle of mercury. The trajectories are categorized into 4 sectors. Cluster 1 and cluster 4 were the main routes of dust to Qingdao, coming from Kazakhstan and north of Mongolia individually. There is higher TSP, and lower PHg/TSP in dust of cluster 4 compared with cluster 1, because of longer transport distance and faster movement speed. There is highest PHg/TSP in cluster 2 because of passing polluted East China. The slow transport speed, long stay at polluted developed region caused pollutants to accumulate in the aerosols. Differences of transport route, movement speed affects the mercury content significantly.

  17. A study of the association between atmospheric particulate matter and blood pressure in the population.

    Science.gov (United States)

    Zhang, Huawei; Qian, Jin; Zhao, Haiping; Wang, Jinda; Zhu, Hang; Zhou, Ying; Wang, Juan; Guo, Jin; Gehendra, Mahara; Qiu, Hongyan; Sun, Zhijun; He, Dian

    2016-06-01

    This systematic review and meta-analysis was conducted to assess the association between the level of atmospheric particulate matter (PM) and the increase in blood pressure (BP) for different exposure terms (≤ 7 vs > 7 days) and age groups (levels and higher BP. The β values were 0.270mmHg (95% confidence interval [CI] 0.068-0.482) for SBP and 0.215mmHg (95% CI 0.058-0.372) for DBP. These β values mean that, for every 10 mg/m(3) increase in PM10, SBP increased by 0.270mmHg and DBP by 0.215 mmHg. Subgroup analyses were conducted for different exposure terms and age groups. A positive association was seen between PM2.5 and SBP. The β value of SBP was 0.495mmHg (95% CI 0.03-0.96) with every 10 mg/m(3) increase in PM2.5. There were no significant associations in both age groups and non-older groups. There was no significant association between PM2.5 and DBP, either in the overall effect or in the subgroup effects. In conclusion, significant associations were found between higher BP and higher PM10 levels, but the association between BP and levels of PM2.5 levels was unclear. PMID:26634767

  18. In-situ partitioning and bioconcentration of polycyclic aromatic hydrocarbons among water, suspended particulate matter, and fish in the Dongjiang and Pearl Rivers and the Pearl River Estuary, China

    International Nuclear Information System (INIS)

    Highlights: • PAHs are relatively higher in marine fish than in freshwater fish. • PAHs respectively show significant correlations with DOC, POC, and Chl a. • The log Koc for PAHs is one order magnitude higher than the predicted. • The log BCF values in fish and their tissues are nonlinear in respect to log Kow. • Lipid is related to PAHs in freshwater fish, but not in marine fishes. - Abstract: The partitioning and bioaccumulation of polycyclic aromatic hydrocarbons (PAHs) in water, suspended particulate matter (SPM), and fish samples from the Dongjiang River (DR), Pearl River (PR), and the Pearl River Estuary (PRE) were examined. Although PAHs are much lower in PRE than in DR or PR, PAHs in some fish species are significantly higher in PRE than in DR or PR. Aqueous or particulate PAHs respectively show significant correlations with dissolved organic carbon, particulate organic matter, and chlorophyll a, suggesting that biological pumping effect regulates their distribution. The in situ partitioning coefficients (log Koc) for PAHs are one order magnitude higher than the empirical log Koc–log Kow correlation. The bioconcentration factor (BCF) is slightly higher for the marine fish than for the freshwater fish. The above phenomena indicate that BCF may vary due to the diversity of fish species, feeding habits, and metabolism of PAHs in fish

  19. Origin of particulate organic carbon in the marine atmosphere as indicated by it stable carbon isotopic composition

    International Nuclear Information System (INIS)

    Organic carbon concentration and isotopic composition were determined in samples of atmospheric particulate matter collected in 1979 at remote marine locations (Enewetak atoll, Sargasso Sea) during the SEAREX (Sea-Air Exchange) program field experiments. Atmospheric Particulate Organic Carbon (POC) concentrations were found to be in the range of 0.3 to 1.2 mg. m-3, in agreement with previous literature data. The major mass of POC was found on the smallest particles (r13C/12C of the small particles is close to the one expected (d13C = 26 +- 20//sub infinity/) for atmospheric POC of continental origin. For all the samples analysed so far, it appears that more than 80% of atmospheric POC over remote marine areas is of continental origin. This can be explained either by long-range transport of small sized continental organic aserosols or by the production of POC in the marine atmosphere from a vapor phase organic carbon pool of continental origin. The POC in the large size fraction of marine aerosols (13C = -21 +- 20/00) for POC associated with sea-salt droplets transported to the marine atmosphere

  20. Characteristics of particulate radionuclides in the atmospheric surface layer of the 30-km zone of Chernobyl

    International Nuclear Information System (INIS)

    For the inhalation dose assessment, reliable estimations are necessary of the average volume concentration of particle bound radionuclides in the atmosphere specifying the nuclide composition, the activity distribution in the different particle size ranges and the solubility characteristics of the nuclides. For that purpose, the analysis of measurement series is presented of the daily average activity concentrations of 137Cs and 144Ce and their temporal and spatial variability. From 1986 till 1994, samples were taken with high-volume samplers and multicascade impactors; the number concentrations of aerosol particles and the number concentrations of 'hot' particles were determined for different conditions with an Aerosol Particle Sizer and a Rotating Arm Impactor. The data demonstrate a decrease the atmospheric concentrations of 137Cs and 144Ce with time larger than caused by radioactive decay alone. A statistical analysis showed a high level of fluctuations in the concentration of radionuclides in air with maxima exceeding the annual average by 10 to 20 times. The analysis of 88 experimental radioactivity size distributions at Zapolie and Pripyat for winddriven resuspension conditions have shown that the measured distributions are generally very wide and differ from the log-normal distribution in the most cases. At Zapolie, the mean air concentrations of 137Cs, discriminated in four size ranges, showed an increasing part of inhalable particles with time since the accident. In 1993, the inhalable fraction was about 48% of the total concentration. The size distribution of atmospheric 137Cs particulate activity during these periods of enhanced resuspension showed a similar common shape with two maxima, the first in the 2-4 μm range, and the second in the 12-20 μm range. The estimated radioactive loading of particles showed an enrichment of resuspended radionuclides compared with soil particles. The highest enrichment factor was found for large particles, the lowest

  1. Determination of Si, Al and Fe in atmospheric particulate material by 14-MeV neutron activation analysis

    International Nuclear Information System (INIS)

    Concentrations of Si, Al and Fe were determined in atmospheric particulate material using 14 MeV neutron activation analysis, at the levels at which they normally exist. Enrichment factor and the importance of Al and Fe as being normalizing elements were discussed. Concentrations of Si, Al and Fe were found to be 20.8+-3.6, 7.20+-1.5 and 2.68 +-0.91 μg/m3 respectively

  2. The iron component of particulate matter is antiapoptotic: A clue to the development of lung cancer after exposure to atmospheric pollutants?

    Science.gov (United States)

    Lovera-Leroux, Melanie; Crobeddu, Belinda; Kassis, Nadim; Petit, Patrice X; Janel, Nathalie; Baeza-Squiban, Armelle; Andreau, Karine

    2015-11-01

    The classification of outdoor air pollution as carcinogenic for humans strengthens the increasing concern about particulate matter (PM). We previously demonstrated that PM exposure produces an antiapoptotic effect resulting from polycyclic aromatic hydrocarbons (PAH) and water-soluble components. In this study, we investigated transition metallic compounds, particularly iron, in order to decipher their underlying molecular mechanisms that prevent apoptosis. Human bronchial epithelial cells were exposed for 4 h to different PM samples with established antiapoptotic effect (e.g. PM-AW) or not (e.g. PM-VS) or to their metallic components (Fe, Mn, Zn and Al) before apoptosis induction by the calcium ionophore A23187 or Staurosporine. PM-AW, Fe, Mn and Al significantly reduced induced apoptosis. The antiapoptotic effect of Fe was enhanced by benzo(a)pyrene, a typical PAH compound, but was totally reversed by the iron chelator, deferiprone. Furthermore, particles and iron triggered cellular ROS generation and prevented the depletion in glutathione levels observed during A23187-induced apoptosis. In contrast to benzo(a)pyrene, PM-AW and Fe rapidly activated NRF2, subsequently upregulated several target genes (HO1, NQO1 and GPX1) and modulated some genes which control cell death (BCL2, BAX and p53). The key role of the NRF2 pathway in the antiapoptotic effect mediated by Fe and PM was demonstrated using siRNA technology. Our results suggest that the iron component participates in the antiapoptotic effect of PM by activating a NRF2-dependent antioxidant process. As resisting to cell death is one of the hallmarks of cancer cells, these findings provide additional clues for understanding the development of lung cancer after atmospheric pollution exposure. PMID:26419736

  3. Atmospheric concentrations and dry deposition fluxes of particulate trace metals in Salvador, Bahia, Brazil

    Science.gov (United States)

    de P. Pereira, Pedro A.; Lopes, Wilson A.; Carvalho, Luiz S.; da Rocha, Gisele O.; de Carvalho Bahia, Nei; Loyola, Josiane; Quiterio, Simone L.; Escaleira, Viviane; Arbilla, Graciela; de Andrade, Jailson B.

    Respiratory system is the major route of entry for airborne particulates, being the effect on the human organism dependent on chemical composition of the particles, exposure time and individual susceptibility. Airborne particulate trace metals are considered to represent a health hazard since they may be absorbed into human lung tissues during breathing. Fossil fuel and wood combustion, as well as waste incineration and industrial processes, are the main anthropic sources of metals to the atmosphere. In urban areas, vehicular emissions—and dust resuspension associated to road traffic—become the most important manmade source. This work investigated the atmospheric concentrations of TSP, PM 10 and elements such as iron, manganese, copper and zinc, from three different sites around Salvador Region (Bahia, Brazil), namely: (i) Lapa Bus Station, strongly impacted by heavy-duty diesel vehicles; (ii) Aratu harbor, impacted by an intense movement of goods, including metal ores and concentrates and near industrial centers and; (iii) Bananeira Village located on Maré Island, a non-vehicle-influenced site, with activities such as handcraft work and fishery, although placed near the port. Results have pointed out that TSP concentrations ranged between 16.9 (Bananeira) and 354.0 μg m -3 (Aratu#1), while for PM 10 they ranged between 30.9 and 393.0 μg m -3, both in the Lapa Bus Station. Iron was the major element in both Lapa Station and Aratu (#1 and #2), with average concentrations in the PM 10 samples of 148.9, 79.6 and 205.0 ng m -3, respectively. Zinc, on the other hand, was predominant in samples from Bananeira, with an average concentration of 145.0 ng m -3 in TSP samples, since no PM 10 sample was taken from this site. The main sources of iron in the Lapa Station and Aratu harbor were, respectively, soil resuspension by buses and discharge of solid granaries, as fertilizers and metal ores. On the other hand, zinc and copper in the bus station were mainly from

  4. 40 CFR Appendix J to Part 50 - Reference Method for the Determination of Particulate Matter as PM10 in the Atmosphere

    Science.gov (United States)

    2010-07-01

    ... of Particulate Matter as PM10 in the Atmosphere J Appendix J to Part 50 Protection of Environment... as PM10 in the Atmosphere 1.0 Applicability. 1.1 This method provides for the measurement of the mass... particle distribution in the atmosphere during the sampling period. The use of a flow control...

  5. Reactive Oxygen Species Generation Linked to Sources of Atmospheric Particulate Matter and Cardiorespiratory Effects.

    Science.gov (United States)

    Bates, Josephine T; Weber, Rodney J; Abrams, Joseph; Verma, Vishal; Fang, Ting; Klein, Mitchel; Strickland, Matthew J; Sarnat, Stefanie Ebelt; Chang, Howard H; Mulholland, James A; Tolbert, Paige E; Russell, Armistead G

    2015-11-17

    Exposure to atmospheric fine particulate matter (PM2.5) is associated with cardiorespiratory morbidity and mortality, but the mechanisms are not well understood. We assess the hypothesis that PM2.5 induces oxidative stress in the body via catalytic generation of reactive oxygen species (ROS). A dithiothreitol (DTT) assay was used to measure the ROS-generation potential of water-soluble PM2.5. Source apportionment on ambient (Atlanta, GA) PM2.5 was performed using the chemical mass balance method with ensemble-averaged source impact profiles. Linear regression analysis was used to relate PM2.5 emission sources to ROS-generation potential and to estimate historical levels of DTT activity for use in an epidemiologic analysis for the period of 1998-2009. Light-duty gasoline vehicles (LDGV) exhibited the highest intrinsic DTT activity, followed by biomass burning (BURN) and heavy-duty diesel vehicles (HDDV) (0.11 ± 0.02, 0.069 ± 0.02, and 0.052 ± 0.01 nmol min(-1) μg(-1)source, respectively). BURN contributed the largest fraction to total DTT activity over the study period, followed by LDGV and HDDV (45, 20, and 14%, respectively). DTT activity was more strongly associated with emergency department visits for asthma/wheezing and congestive heart failure than PM2.5. This work provides further epidemiologic evidence of a biologically plausible mechanism, that of oxidative stress, for associations of adverse health outcomes with PM2.5 mass and supports continued assessment of the utility of the DTT activity assay as a measure of ROS-generating potential of particles. PMID:26457347

  6. Molecular composition of sugars in atmospheric particulate matter from interior Alaska

    Science.gov (United States)

    Haque, Md. Mozammel; Kawamura, Kimitaka; Kim, Yongwon

    2015-04-01

    Sugars can account for 0.5-8% of carbon in atmospheric particulate matter, affecting the earth climate, air quality and public health. Total of 33 total suspended particle (TSP) samples were collected from Fairbanks, Alaska in June 2008 to June 2009 using a low volume air sampler. Here, we report the molecular characteristics of anhydro-sugars (levoglucosan, galactosan and mannosan), primary saccharides (xylose, fructose, glucose, sucrose and trehalose) and sugar alcohols (erythritol, arabitol, mannitol and inositol). The average contribution of sugars to the organic carbon (OC) was also determined to be 0.92%. Sugar compounds were measured using solvent extraction/TMS-derivatization technique followed by gas chromatography-mass spectrometry (GC-MS) determination. The concentrations of total quantified sugar compounds ranged from 2.3 to 453 ng m-3 (average 145 ng m-3). The highest concentration was recorded for levoglucosan in summer, with a maximum concentration of 790 ng m-3 (average 108 ng m-3). Levoglucosan, which is specifically formed by a pyrolysis of cellulose, has been used as an excellent tracer of biomass burning. The highest level of levoglucosan indicates a significant contribution of biomass burning in ambient aerosols. Galactosan (average 20 ng m-3) and mannosan (average 27 ng m-3), which are also formed through the pyrolysis of cellulose/hemicelluloses, were identified in all samples. The average concentrations of arabitol, mannitol, glucose and sucrose were also found 14.7, 14.6, 14.1 and 16.8 ng m-3, respectively. They have been proposed as tracers for resuspension of surface soil and unpaved road dust, which contain biological materials including fungi and bacteria. These results suggest that there is some impact of bioaerosols on climate over Interior Alaska. We will also measure water-soluble organic carbon (WSOC) and inorganic ions for all samples.

  7. A Preliminary Assessment of Chemical Constituents of Atmospheric Particulate Matter and their Sources in Faisalabad, Pakistan

    International Nuclear Information System (INIS)

    Atmospheric total suspended particulate matter (TSP) mass and chemical constituents were characterized, collected on glass fiber filters using high volume air sampler in Faisalabad, Pakistan from May 2012 to April 2013. Two receptor models Principal Component Analysis (PCA) and UNMIX were used for the source identification in the study area. High volume TSP samples (n=288) were subjected to gravimetric and quantitative chemical analyses for determining trace elements (Pb, Cd, Ni, Zn, Cu, Fe) using atomic absorption spectroscopy and water-soluble cations (Ca/sup 2+/, Mg/sup 2+/, Na/sup +/, K/sup +/, NH/sub 4/ /sup +/) and anions (Cl/sup -/, SO/sub 4/ /sup 2-/ and NO/sub 3 /sup -/) by ion chromatography. The average TSP concentration was 575 meu g m/sup -3/ that is 1.6 and 8 times higher than Pak NEQS (360 meu g m/sup -3/) and US EPA (75 meu g m/sup -3/) annual limits, respectively. The crustal elements Ca, Fe, Mg and Na were the largest contributors to TSP mass while elements of anthropogenic origin Pb, Cd, Ni, Cu and Zn had relatively lower concentrations. The enrichment factors (EFs) for elements indicated that Pb, Cd, Cu, Zn and Ni (with EFs>100) were highly enriched and are of anthropogenic origin. Both PCA and UNMIX models produced comparable factor compositions and identified four possible sources: (1) crude oil combustion, (2) re-suspended crustal/road dust, (3) combination of coal and biomass burning and (4) secondary particles. Results of EF, cluster analysis and correlation analysis also duly supported the model results of source identification. (author)

  8. Bulky PAH-DNA induced by exposure of a co-culture model of human alveolar macrophages and embryonic epithelial cells to atmospheric particulate pollution

    International Nuclear Information System (INIS)

    Because of their deep penetration in human lungs, fine airborne particulate matter were described as mainly responsible for the deleterious effects of exposure to air pollution on health. Organic constituents are adsorbed on particles surface and, after inhalation, some (polycyclic aromatic hydrocarbons, PAHs) can be activated into reactive metabolites and can bind to DNA. The formation of bulky DNA adducts has been researched after exposure of mono-and co-cultures of alveolar macrophages (AM) and human embryonic human lung epithelial (L132), to fine air pollution particulate matter Air samples have been collected with cascade impactor and characterized: size distribution (92.15% 2/g), inorganic (Fe, AI, Ca, Na, K, Mg, Pb, etc.) and organic compounds (PAHs, etc.). 32P post-labeling method was applied to detect bulky DNA adducts in AM and L132, in mono-and co-cultures, 72 h after their exposure to atmospheric particles at their Lethals and Effects concentrations or (LC or CE) to 50% (i.e. MA: EC50 = 74.63 μg/mL and L132: LC-5-0 = 75.36 μg/mL). Exposure to desorbed particles (MA: C1= 61.11 μg/mL and L132 : C2 = 61.71 μg/mL) and B[a]P (1 μM) were included. Bulky PAH-DNA adducts were detected in AM in mono-culture after exposure to total particles (Pt), to B[a]P and desorbed particles (Pd). Whatever the exposure, no DNA adduct was detected in L132 in mono-culture. These results are coherent with the enzymatic activities of cytochrome P450 l Al in AM and L132. Exposure of co-culture to Pt, or Pd induced bulky adducts to DNA in AM but not in L132. Exposure to B[a]P alone has altered the DNA of AM and L132, in co-culture. Exposure to Pt is closer to the environmental conditions, but conferred an exposure to amounts of genotoxic agents compared to studies using organic extracts. The formation of bulky DNA adducts was nevertheless observed in AM exposed to Pt, in mono- or co-culture, indicating that they were competent in terms of metabolic activation of PAHs. The DNA

  9. Organic composition of size segregated atmospheric particulate matter, during summer and winter sampling campaigns at representative sites in Madrid, Spain

    Science.gov (United States)

    Mirante, Fátima; Alves, Célia; Pio, Casimiro; Pindado, Oscar; Perez, Rosa; Revuelta, M.a. Aranzazu; Artiñano, Begoña

    2013-10-01

    Madrid, the largest city of Spain, has some and unique air pollution problems, such as emissions from residential coal burning, a huge vehicle fleet and frequent African dust outbreaks, along with the lack of industrial emissions. The chemical composition of particulate matter (PM) was studied during summer and winter sampling campaigns, conducted in order to obtain size-segregated information at two different urban sites (roadside and urban background). PM was sampled with high volume cascade impactors, with 4 stages: 10-2.5, 2.5-1, 1-0.5 and < 0.5 μm. Samples were solvent extracted and organic compounds were identified and quantified by GC-MS. Alkanes, polycyclic aromatic hydrocarbons (PAHs), alcohols and fatty acids were chromatographically resolved. The PM1-2.5 was the fraction with the highest mass percentage of organics. Acids were the organic compounds that dominated all particle size fractions. Different organic compounds presented apparently different seasonal characteristics, reflecting distinct emission sources, such as vehicle exhausts and biogenic sources. The benzo[a]pyrene equivalent concentrations were lower than 1 ng m- 3. The estimated carcinogenic risk is low.

  10. Thermodynamics of the formation of atmospheric organic particulate matter by accretion reactions—2. Dialdehydes, methylglyoxal, and diketones

    Science.gov (United States)

    Barsanti, Kelley C.; Pankow, James F.

    Predicting the formation of organic particulate matter (OPM) in the atmosphere by absorptive gas/particle partitioning requires a knowledge of the identities, atmospheric levels, and physical properties of all condensable species. Data from field and chamber experiments have shown that a portion of atmospheric OPM samples are comprised of products generated during oxidation of volatile organic compounds. It has been suggested that some of these initially formed oxidation products also contribute to the formation of atmospheric OPM via molecular-weight (MW) building "accretion reactions". The role of such reactions as well as a general theoretical approach for evaluating their thermodynamic relevance in regard to atmospheric OPM formation, have been discussed in prior work. This work utilizes that approach in considerations of accretion reactions of glyoxal, two other dialdehydes, methylglyoxal, and two diketones. The methods used to predict free energy of formation ( ΔG°) values (and hence equilibrium constant ( K) values) indicate that: (1) for 1,4-butanedial, 2,3-butanedione, and 2,5-hexanedione, the accretion reactions considered are not favorable; (2) for C 6 and higher dialdehydes, reaction by aldol condensation may contribute to atmospheric OPM formation under certain circumstances, if kinetically favorable; and (3) for glyoxal, diol and subsequent oligomer formation, and for methylglyoxal, aldol condensation, are thermodynamically favorable, and may contribute significantly to OPM in the atmosphere, if kinetically favorable.

  11. Analytical Procedure Development to Determine Polycyclic Aromatic Compounds in the PM2.5-PM10 Fraction of Atmospheric Aerosols

    International Nuclear Information System (INIS)

    This paper presents an optimized and validated analytical methodology for the determination of various polycyclic aromatic compounds in ambient air using liquid chromatography with fluorescence detection. This analysis method was applied to samples obtained during more than one year in an area of Madrid. Selected compounds have included thirteen polycyclic hydrocarbons considered priorities by the EPA, and hydroxylated derivatives, which have been less investigated in air samples by liquid chromatography with fluorescence detection. We have characterized and compared the concentration ranges of compounds identified and studied seasonal and monthly variations. In addition, the techniques have been applied to study multivariate correlations, factor analysis and cluster analysis to extract as much information as possible for interpretation and more complete and accurate characterization of the results and their relationship with meteorological parameters and physicochemical. (Author)

  12. Health assessment document for polycyclic organic matter. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Santodonato, J.; Howard, P.; Basu, D.; Lande, S.; Selkirk, J.K.

    1979-02-01

    The document responds to Section 122 of the Clean Air Act as Amended August 1977, which requires the Administrator to decide whether atmospheric emissions of polycyclic organic matter (POM) potentially endanger public health. This document reviews POM data on chemical and physical properties, atmospheric forms, atmospheric fate and transport, measurement techniques, ambient levels, toxicology, occupational health, and epidemiology. Polycyclic aromatic hydrocarbons (PAH's), such as the carcinogen benzo(a)pyrene (BaP), and their neutral nitrogen analogs are the two POM chemical groups occurring most frequently in ambient air. The major environmental sources of POM's appear to be the combustion or pyrolysis of materials containing carbon and hydrogen. There is general agreement that POM compounds are associated with suspended particulate matter from both mobile and stationary sources, principally respirable particles. Available monitoring data suggest that many POM compounds associated with particulate matter probably are stable in ambient air for several days. The major health concern over exposure to POM's is their carcinogenicity. POM's gain ready access to the body's circulation either by inhalation, ingestion, or skin contact. Although it cannot be stated unequivocally that any POM's are human carcinogens, several of these compounds are among the more potent animal carcinogens known.

  13. Gas-phase and particulate products from the atmospheric degradation of the organothiophosphorus insecticide chlorpyrifos-methyl.

    Science.gov (United States)

    Borrás, Esther; Tortajada-Genaro, Luis Antonio; Ródenas, Milagros; Vera, Teresa; Coscollá, Clara; Yusá, Vicent; Muñoz, Amalia

    2015-11-01

    The phosphorothioate structure is highly present in several organophosphorus pesticides. However, there is insufficient information about its degradation process after the release to the atmosphere and the secondary pollutants formed. Herein, the atmospheric reaction of chlorpyrifos-methyl (o,o-dimethyl o-(3,5,6-trichloropyridin-2-yl) phosphorothioate), is described for semi-urban or rural locations. The photo-oxidation under low NOx conditions (5-55 ppbV) was reproduced in a large outdoor simulation chamber, observing a rapid degradation (lifetime<3.5 h). The formation of gaseous products and particulate matter (aerosol yield 2-8%) was monitored. The chemical composition of minor products (gaseous and particulate) was studied, identifying 15 multi-oxygenated derivatives. The most abundant products were ring-retaining molecules such as o,o-dimethyl o-(3,5,6-trichloropyridin-2-yl) phosphorothioate, dimethyl 3,5,6-trichloropyridin-2-yl phosphate, o-methyl o-(3,5,6-trichloropyridin-2-yl) hydrogen phosphorothioate, 3,5,6-trichloropyridin-2-yl dihydrogen phosphate, 3,5,6-trichloropyridin-2-ol, and 3,5,6-trichloropyridine-2,4-diol. An atmospheric degradation mechanism has been proposed based on an oxidation started with OH-nucleophilic attack to P=S bond. The results have been extrapolated to other organothiophosphorus molecules, such as malathion, parathion, diazinon and methidathion, among many others, to estimate their photo-oxidative degradation and the expected products. PMID:25548033

  14. Characteristics of atmospheric particulate mercury in size-fractionated particles during haze days in Shanghai

    Science.gov (United States)

    Chen, Xiaojia; Balasubramanian, Rajasekhar; Zhu, Qiongyu; Behera, Sailesh N.; Bo, Dandan; Huang, Xian; Xie, Haiyun; Cheng, Jinping

    2016-04-01

    Atmospheric particulate mercury (PHg) is recognized as a global pollutant that requires regulation because of its significant impacts on both human health and wildlife. The haze episodes that occur frequently in China could influence the transport and fate of PHg. To examine the characteristics of PHg during haze and non-haze days, size-fractioned particles were collected using thirteen-stage Nano-MOUDI samplers (10 nm-18 μm) during a severe haze episode (from December 2013 to January 2014) in Shanghai. The PHg concentration on haze days (4.11 ± 0.53 ng m-3) was three times higher than on non-haze days (1.34 ± 0.15 ng m-3). The ratio of the PHg concentration to total gaseous mercury (TGM) ranged from 0.42 during haze days to 0.21 during non-haze days, which was possibly due to the elevated concentration of particles for gaseous elemental mercury (GEM) adsorption, elevated sulfate and nitrate contributing to GEM oxidation, and the catalytic effect of elevated water-soluble inorganic metal ions. PHg/PM10 during haze days (0.019 ± 0.004 ng/μg) was lower than during non-haze days (0.024 ± 0.002 ng/μg), and PHg/PM10 was significantly reduced with an increasing concentration of PM10, which implied a relatively lower growth velocity of mercury than other compositions on particles during haze days, especially in the diameter range of 0.018-0.032 μm. During haze days, each size-fractioned PHg concentration was higher than the corresponding fraction on non-haze days, and the dominant particle size was in the accumulation mode, with constant accumulation to a particle size of 0.56-1.0 μm. The mass size distribution of PHg was bimodal with peaks at 0.32-0.56 μm and 3.1-6.2 μm on non-haze days, and 0.56-1.0 μm and 3.1-6.2 μm on haze days. There was a clear trend that the dominant size for PHg in the fine modes shifted from 0.32-0.56 μm during non-haze days to 0.56-1.0 μm on haze days, which revealed the higher growth velocity of PHg on haze days due to the

  15. Atmospheric particulate matter and hospital admission due to lower respiratory tract infection: a case-cross study in Shijiazhuang, China

    Directory of Open Access Journals (Sweden)

    Zi-na BAI

    2016-03-01

    Full Text Available Objective  To explore the association between atmospheric particulate matter (PM10/PM2.5 levels and hospital admissions due to lower respiratory tract infection in Shijiazhuang. Methods  Data of air pollution, meteorologic data, and the data of patients admitted to hospital due to lower respiratory tract infection were retrospectively analyzed. Pearson's correlation coefficients were calculated to analyze correlations between atmospheric particulate matter and meteorologic factors. Data of hospital admission due to lower respiratory tract infection and of atmospheric air pollution levels in Shijiazhuang were obtained, a bidirectional case-crossover design was used to investigate the association between hospital admissions due to lower respiratory tract infection and levels of atmospheric particles. Stratified analyses of exposure based on age, gender, complications and season were performed to evaluate the effect. Results  Pearson's correlation analysis showed positive correlations among PM2.5, PM10, SO2, NO2 and CO. The concentration of all these five pollutants were negatively correlated with O3 and daily mean temperature, while a positive correlation was found between concentrations of the 5 pollutants and daily average temperature and O3. In single-pollutant model, every 10μg/m3 increase in PM2.5 and PM10 at lag5 brought the corresponding OR values (95%CI up to 1.010(1.005-1.015 and 1.006(1.003-1.009 respectively. In the multi-pollutant models, the observed effects of PM2.5 remained significant. Stratified analysis based on gender, age, season and comorbidities showed that the effect of PM2.5 exposure on lower respiratory tract infection admissions was stronger in males, persons younger than 60 years of age and persons without comorbidities, and even more stronger in cold season. The effect of PM10 exposure on lower respiratory tract infection admissions was stronger in females, persons older than 60 years of age and persons with

  16. Correlation of trace element content in air particulates with solar meteorological data in the atmosphere of Athens

    International Nuclear Information System (INIS)

    Relation between the trace element content in air particulates and solar meteorological data in the atmospheric environment of Athens, Greece, was studied. For this purpose, Sm, Br, As, Na, K, La, Ce, Cr, Ag, Sc, Fe, Zn, Co, Sb, Th were determined by INAA in respirable aerosols collected during winter 1993-1994. The results showed that the average cloudiness, sunshine, and the total solar radiation (sun and sky) on a horizontal surface, (3 variables) have no relation with trace element variation. However, diffuse solar radiation (sun and sky) on a horizontal surface seems to have statistically significant relationship with some of the trace element variation. It forms a single component with some trace elements after the application of the factor analysis. The increase of the same solar variable in the Athens City center, is one of the factors which cannot permit the emission of trace elements in the atmospheric environment from dust soil and car tires. (author)

  17. Comparison of hot Soxhlet and accelerated solvent extractions with microwave and supercritical fluid extractions for the determination of polycyclic aromatic hydrocarbons and nitrated derivatives strongly adsorbed on soot collected inside a diesel particulate filter.

    Science.gov (United States)

    Oukebdane, K; Portet-Koltalo, F; Machour, N; Dionnet, F; Desbène, P L

    2010-06-30

    Several methods of extraction were optimized to extract polycyclic aromatic hydrocarbons (PAHs), their nitrated derivatives and heavy n-alkanes from a highly adsorptive particulate matter resulting from the combustion of diesel fuel in a diesel engine. This particular carbonaceous particulate matter, collected at high temperatures in cordierite diesel particulate filters (DPF), which are optimized for removing diesel particles from diesel engine exhaust emissions, appeared extremely refractory to extractions using the classical extracting conditions for these pollutants. In particular, the method of accelerated solvent extraction (ASE) is described in detail here. Optimization was performed through experimental design to understand the impact of each factor studied and the factors' possible interactions on the recovery yields. The conventional extraction technique, i.e., Soxhlet extraction, was also carried out, but the lack of quantitative extractions led us to use a more effective approach: hot Soxhlet. It appeared that the extraction of the heaviest PAHs and nitroPAHs by either the optimized ASE or hot Soxhlet processes was far from complete. To enhance recovery yields, we tested original solvent mixtures of aromatic and heteroaromatic solvents. Thereafter, these two extraction techniques were compared to microwave-assisted extraction (MAE) and supercritical fluid extraction (SFE). In every case, the only solvent mixture that permitted quantitative extraction of the heaviest PAHs from the diesel soot was composed of pyridine and diethylamine, which has a strong electron-donor character. Conversely, the extraction of the nitrated PAHs was significantly improved by the use of an electron-acceptor solvent or by introducing a small amount of acetic acid into the pyridine. It was demonstrated that, for many desirable features, no single extraction technique stound out as the best: ASE, MAE or SFE could all challenge hot Soxhlet for favourable extractions

  18. Trace elements in the atmospheric particulate of Milan and suburban areas. A study carried out by INAA

    International Nuclear Information System (INIS)

    The atmospheric particulate of industrialized cities had become a mixture of potentially toxic substances whose concentrations must be monitored to assess the pollution levels. Trace metals and elements are part of these pollutants and the knowledge of their total concentration in the air as well as their distribution in the different aerosol particle sizes is necessary to evaluate the pollution risk in terms of maximum present levels and long term exposure. In the present work, a preliminary part of a study initiated for monitoring the trace element levels present in the atmospheric particulate of the city of Milan (north Italy) and of its suburban areas is presented. More than 25 elements have been determined in Milan downtown along a period of three years and in different weather conditions. The granulometric distribution of selected potentially toxic elements (such as vanadium, lead, cadmium, nickel) has been also determined to evaluate their concentrations in different inhalable fractions (alveolar and bronchial - tracheal). Instrumental Neutron Activation Analysis (INAA) has been used for the determination of the great part of the elements while Graphite Furnace Atomic Absorption Spectroscopy (GF-AAS) has been employed for the determination of lead and, in some cases, for nickel, cadmium and copper. (author)

  19. Spatial characteristics and major sources of polycyclic aromatic hydrocarbons from soil and respirable particulate matter in a mega-city, China.

    Science.gov (United States)

    Fu, Shan; Yang, Zhong-Zhi; Li, Ke; Xu, Xiao-Bai

    2010-07-01

    As one of China's great metropolises, Taiyuan is generally recognized to be one of the most polluted cities from polycyclic aromatic hydrocarbons (PAHs) in the world. Therefore, this study was conducted to determine a total of 16 PAH concentrations in various environmental media in Taiyuan. The total PAHs concentration ranged from 1.0 to 26 microg g(-1) in soil, 1.2 x 10(2) to 1.4 x 10(3) ng m(-3) in PM 2.5 and 76 to 1.1 x 10(3) ng m(-3) in PM 10, respectively. Furthermore, the primary source of PAHs was coal combustion, but the samples were also affected to varying degrees by traffic emissions. PMID:20440470

  20. Characterisation of atmospheric particulate matter by diffusive gradient in thin film (DGT) technique

    Czech Academy of Sciences Publication Activity Database

    Gregušová, Michaela; Dočekal, Bohumil

    University of Antwerp, 2012. s. 222. [International Symposium on Environmental Analytical Chemistry /37./. 22.05.2012-25.05.2012, Antwerp] R&D Projects: GA ČR GAP503/10/2002; GA ČR(CZ) GAP503/11/2315; GA ČR(CZ) GBP503/12/G147 Institutional research plan: CEZ:AV0Z40310501 Keywords : particulate matter * DGT technique * platinum group metals Subject RIV: CB - Analytical Chemistry, Separation

  1. Molecular characterization of atmospheric particulate organosulfates in three megacities at the middle and lower reaches of the Yangtze River

    Science.gov (United States)

    Wang, Xin Ke; Rossignol, Stéphanie; Ma, Ye; Yao, Lei; Wang, Ming Yi; Chen, Jian Min; George, Christian; Wang, Lin

    2016-02-01

    PM2.5 filter samples have been collected in three megacities at the middle and lower reaches of the Yangtze River: Wuhan (WH), Nanjing (NJ), and Shanghai (SH). The samples were analyzed using ultra-high-performance liquid chromatography (UHPLC) coupled with Orbitrap mass spectrometry (MS), which allowed for detection of about 200 formulas of particulate organosulfates (OSs), including dozens of formulas of nitrooxy-organosulfates, with various numbers of isomers for each tentatively determined formula at each location. The number of aliphatic OS formulas represented more than 78 % of the detected OSs at the three locations, while aromatic OSs were much less numerous. OSs with two to four isomers accounted for about 50 % of the total OSs on average in these megacity samples, and the percentage of OSs with six and more isomers in the WH sample was more significant than those in the SH and NJ samples. Additionally, the molecular formula, average molecular weight, and degrees of oxidation and unsaturation of tentatively assigned OSs were compared. The results indicate that the OSs between NJ and SH shared higher similarity, and the characteristics of OSs in SH varied diurnally and seasonally. OSs derived from isoprene, monoterpenes, and sesquiterpenes were abundant in samples from the three megacities and could be produced through both daytime photochemistry and NO3 night-time chemistry. The reaction pathways leading to isoprene-derived OSs probably varied in those locations because of the different NOx levels. In addition, a number of OSs that might be formed from polycyclic aromatic hydrocarbons were also detected, which underlies the importance of anthropogenic sources for this class of compounds.

  2. Determination of gaseous and particulate carbonyls (glycolaldehyde, hydroxyacetone, glyoxal, methylglyoxal, nonanal and decanal) in the atmosphere at Mt. Tai

    Science.gov (United States)

    Kawamura, K.; Okuzawa, K.; Aggarwal, S. G.; Irie, H.; Kanaya, Y.; Wang, Z.

    2013-05-01

    Gaseous and particulate semi-volatile carbonyl compounds were determined every three hours in the atmosphere of Mount Tai (elevation, 1534 m) in the North China Plain during 2-5, 23-24 and 25 June 2006 under clear sky conditions. Using a two-step filter cartridge in a series, particulate carbonyls were first collected on a quartz filter and then gaseous carbonyls were collected on a quartz filter impregnated with O-benzylhydroxylamine (BHA). After the two-step derivatization with BHA and N,O-Bis(trimethylsilyl)trifluoroacetamide (BSTFA), carbonyl derivatives were measured using a gas chromatography. The gaseous concentrations were obtained as follow: glycolaldehyde (range 0-826 ng m-3, average 303 ng m-3), hydroxyacetone (0-579 ng m-3, 126 ng m-3), glyoxal (46-1200 ng m-3, 487 ng m-3), methylglyoxal (88-2690 ng m-3, 967 ng m-3), n-nonanal (0-500 ng m-3, 89 ng m-3), and n-decanal (0-230 ng m-3, 39 ng m-3). These concentrations are among the highest ever reported in the urban and forest atmosphere. We found that gaseous α-dicarbonyls (glyoxal and methylglyoxal) are more than 20 times more abundant than particulate carbonyls and that glycolaldehyde is one order of magnitude more abundant than in aerosol phase. In contrast, hydroxyacetone and normal aldehydes (nonanal and decanal) are equally present in both phases. Time-resolved variations of carbonyls did not show any a clear diurnal pattern, except for hydroxyacetone. We found that glyoxal, methylglyoxal and glycolaldehyde positively correlated with levoglucosan (a tracer of biomass burning), suggesting that a contribution from field burning of agricultural wastes (wheat crops) is significant for the bifunctional carbonyls in the atmosphere of Mt. Tai. Upward transport of the pollutants to the mountaintop from the low lands in the North China Plain is a major process to control the distributions of carbonyls in the upper atmosphere over Mt. Tai.

  3. On-line characterization of gaseous and particulate organic analytes using atmospheric pressure chemical ionization mass spectrometry

    International Nuclear Information System (INIS)

    A modified atmospheric pressure chemical ionization ion source is applied for direct analysis of volatile or low volatile organic compounds in air. The method is based on the direct introduction of the analytes in the gas phase and/or particle phase into the ion source of a commercial ion-trap mass spectrometer. Two methods are employed for the production of primary ions at atmospheric pressure, photoionization and corona discharge. It is shown that in the presence of a dopant, photoionization can be a highly efficient ionization method also for real-time analysis with detection limits for selected analytes in the lower ppt-range. Using corona discharge for the production of primary ions, which is instrumentally easier since no additional chemicals have to be added to the sample flow, we demonstrate the analytical potential of on-line atmospheric pressure chemical ionization mass spectrometry for reaction monitoring experiments. To do so, an atmospherically relevant gas phase reaction is carried out in a 500 l reaction chamber and gaseous and particulate compounds are monitored in the positive and negative ion mode of the mass spectrometer

  4. Estimating the influence of different urban canopy cover types on atmospheric particulate matter (PM10) pollution abatement in London UK.

    Science.gov (United States)

    Tallis, Matthew; Freer-Smith, Peter; Sinnett, Danielle; Aylott, Matthew; Taylor, Gail

    2010-05-01

    In the urban environment atmospheric pollution by PM10 (particulate matter with a diameter less than 10 x 10-6 m) is a problem that can have adverse effects on human health, particularly increasing rates of respiratory disease. The main contributors to atmospheric PM10 in the urban environment are road traffic, industry and power production. The urban tree canopy is a receptor for removing PM10s from the atmosphere due to the large surface areas generated by leaves and air turbulence created by the structure of the urban forest. In this context urban greening has long been known as a mechanism to contribute towards PM10 removal from the air, furthermore, tree canopy cover has a role in contributing towards a more sustainable urban environment. The work reported here has been carried out within the BRIDGE project (SustainaBle uRban plannIng Decision support accountinG for urban mEtabolism). The aim of this project is to assess the fluxes of energy, water, carbon dioxide and particulates within the urban environment and develope a DSS (Decision Support System) to aid urban planners in sustainable development. A combination of published urban canopy cover data from ground, airborne and satellite based surveys was used. For each of the 33 London boroughs the urban canopy was classified to three groups, urban woodland, street trees and garden trees and each group quantified in terms of ground cover. The total [PM10] for each borough was taken from the LAEI (London Atmospheric Emissions Inventory 2006) and the contribution to reducing [PM10] was assessed for each canopy type. Deposition to the urban canopy was assessed using the UFORE (Urban Forest Effects Model) approach. Deposition to the canopy, boundary layer height and percentage reduction of the [PM10] in the atmosphere was assessed using both hourly meterological data and [PM10] and seasonal data derived from annual models. Results from hourly and annual data were compared with measured values. The model was then

  5. Determination of polycyclic aromatic hydrocarbons and their nitro-, amino-derivatives absorbed on particulate matter 2.5 by multiphoton ionization mass spectrometry using far-, deep-, and near-ultraviolet femtosecond lasers.

    Science.gov (United States)

    Tang, Yuanyuan; Imasaka, Tomoko; Yamamoto, Shigekazu; Imasaka, Totaro

    2016-06-01

    Multiphoton ionization processes of parent-polycyclic aromatic hydrocarbons (PPAHs), nitro-PAHs (NPAHs), and amino-PAHs (APAHs) were examined by gas chromatography combined with time-of-flight mass spectrometry using a femtosecond Ti:sapphire laser as the ionization source. The efficiency of multiphoton ionization was examined using lasers emitting in the far-ultraviolet (200 nm), deep-ultraviolet (267 nm), and near-ultraviolet (345 nm) regions. The largest signal intensities were obtained when the far-ultraviolet laser was employed. This favorable result can be attributed to the fact that these compounds have the largest molar absorptivities in the far-ultraviolet region. On the other hand, APAHs were ionized more efficiently than NPAHs in the near-ultraviolet region because of their low ionization energies. A sample extracted from a real particulate matter 2.5 (PM2.5) sample was measured, and numerous signal peaks arising from PAH and its analogs were observed at 200 nm. On the other hand, only a limited number of signed peaks were observed at 345 nm, some of which were signed to PPAHs, NPAHs, and APAHs. Thus, multiphoton ionization mass spectrometry has potential for the use in comprehensive analysis of toxic environmental pollutants. PMID:26971178

  6. Identification, abundance and origin of atmospheric organic particulate matter in a Portuguese rural area

    Science.gov (United States)

    Pio, C. A.; Alves, C. A.; Duarte, A. C.

    Respirable suspended particles high-volume samples were collected from a coastal-rural site in the centre of Portugal in August 1997 and their solvent-extractable organic compounds were subjected to characterisation by gas chromatography-mass spectrometry. Particles were also analysed by a thermal/optical technique in order to determine their black and organic carbon content. The total lipid extract yields ranged from 20 to 63 μg m -3, containing mainly aliphatic hydrocarbons such as n-alkanes, acids, alcohols, aldehydes, ketones and polycyclic aromatic hydrocarbons. The higher input of vascular plant wax components was demonstrated by the distribution patterns of the n-alkanes, n-alkanoic acids and n-alkanols homologous series, with C max at C 29, C 22/C 24 and C 30, respectively. The CPI values for these series were in the range 1.8-9.7, being indicative of recent biogenic input from microbial lipid residues and flora epicuticular components. Specific natural constituents (e.g. phytosterols, terpenes, etc.) were identified as molecular markers. Some oxidation products from volatile organic precursors were also present in the aerosols. In addition, all samples had a component of petroleum hydrocarbons representing urban and vehicular emissions probably transported from the nearest cities and from the motorway in the vicinity. This data set could be used to make a mass balance with organic carbon, organic extracts and elutable matter, permitting also the comparison with lipid signatures observed for other regions.

  7. Observations of the effect of atmospheric processes on the genotoxic potency of airborne particulate matter

    Energy Technology Data Exchange (ETDEWEB)

    Feilberg, A.; Nielsen, T.; Poulsen, M.W.B. [Riso National Laboratory, Roskilde (Denmark); Binderup, M.-L. [Institute of Food Safety and Toxicology, Danish Veterinary and Food Administration, Soeborg (Denmark); Skov, H. [National Environmental Research Institute, Roskilde (Denmark)

    2002-10-01

    In this study, the relationship between genotoxic potency and the occurrence of polycyclic aromatic hydrocarbons (PAH), including benzo(a)pyrene (BaP), and nitro-PAH in urban and semi-rural air masses has been investigated. The Salmonella/microsome assay has been used as a measure of genotoxic potency. We find that the ratios of BaP/mutagenicity and PAH/mutagenicity are highly variable. The processes responsible for the variation are formation and degradation of mutagens and transport of polluted air masses from heavily industrialized regions. Air masses from Central Europe are shown to be highly enriched in mutagens as well as in PAH and nitro-PAH. However, the mutagenic activity is much more elevated than the PAH levels when these air masses are mixed with local urban air. Part of the variation in the PAH/mutagenicity ratio can be explained by photochemical transformation. Since BaP has been used in the past as an indicator of the carcinogenic risk of airborne particles, it is suggested that the cancer risk of air pollution has to be re-evaluated. (author)

  8. Atmospheric lead pollution in fine particulate matter in Shanghai,China

    Institute of Scientific and Technical Information of China (English)

    LI Xiaolin; ZHANG Yuanxun; TAN Mingguang; LIU Jiangfeng; BAO Liangman; ZHANG Guilin; LI Yan; IIDA Atsuo

    2009-01-01

    The Pb-monitoring program was extended for 6 years from 2002 to 2007 at 17 representative urban sites (6 traffic, 5 industrial, and 6 residential sites), and 3 suburban sites to assess the lead pollution in fine particulate matter (PM2.5) after phasing out leaded gasoline in Shanghai. Compared with Pb levels reported in other places, the Pb pollution in Shanghai still serious after phasing out leaded gasoline, which remains at high concentration range (213--176 ng/m3) in PM2.5 in winter. Significant spatial variation of Pb concentrations and strong seasonal variation of higher Pb concentration in winter than that in summer were detected. The size distribution of Pb in particulate matter has a unimodal mode that peaks at approximately 0.154--1.59 mm particle diameter, indicating that Pb is mainly concentrated in fine fraction. Lead in the fine fraction is enriched by a factor of 103--104 relative to Pb abundance in crust. Eight categories of Pb pollution sources were identified in the PM2.5 in the winter of 2007 in Shanghai. The important emission sources among them are vehicle exhaust derived from combustion of unleaded gasoline, metallurgic industry emission, and coal combustion emission.

  9. High time resolution observation and statistical analysis of atmospheric light extinction properties and the chemical speciation of fine particulates

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    In recent years,the visibility deterioration caused by regional fine particulate pollution becomes one of the crucial air pollution problems in the urban areas of our country.The rapid variation of visibility and fine particulates make it difficult to estimate the relationship between them precisely and accurately unless high time resolution observation data can be accessed.This study aims to fill this gap in the field of atmospheric science by establishing a formula using multiple linear regressions.Excellent fitting goodness (R2=0.913,n=3167) was obtained using 10 min average of high-resolution real-time light scattering coefficients,light absorption coefficients,main chemical speciation concentration in PM1 and some meteorological parameters from 17 Jan to 16 Feb,2009.It shows that the average light extinction coefficient during the observation in the winter of Shenzhen was measured to be 290 ± 183 Mm?1,consisting of 72% of light scattering and 21% of absorption.In terms of the percentage contribution of PM1 chemical species to the total light extinction,the organic matter was estimated to be most with an average of 45%,followed by ammonium sulfate with an average of 24%.The contributions of black carbon and ammonium nitrate were 17% and 12%,respectively.Besides,the diurnal variation of light extinction was investigated as well in this study.

  10. Determination of lead isotopic composition of airborne particulate matter by ICPMS: implications for lead atmospheric emissions in Canada

    International Nuclear Information System (INIS)

    Full text: Quadrupole ICPMS was used for determination of trace metal concentrations and lead isotopic composition in fine particulate matter (PM2.5) collected at selected sites within the Canadian National Air Pollution Surveillance network, from February 2005 to February 2007. High enrichment factors indicated that lead is mostly of anthropogenic origin and consequently, the lead isotopic composition is directly related to that of pollution sources. The 206Pb/207Pb and 208Pb/207Pb ratios were measured and the results were compared to the isotopic signatures of lead from different sources. Various approaches were used to assess the impact of relevant sources and the meteorological conditions in the occurrence and distribution of lead in Canadian atmospheric aerosols. (author)

  11. Polychlorinated biphenyls and organochlorine pesticides in atmospheric particulate matter of Northern China: distribution, sources, and risk assessment.

    Science.gov (United States)

    Ding, Shuangshuang; Dong, Faqin; Wang, Bin; Chen, Shu; Zhang, Liufei; Chen, Mengjun; Gao, Mei; He, Ping

    2015-11-01

    The objectives of this work are to track the contamination levels, distribution characteristics, and sources of polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) in atmospheric particulate matter (APM) of Northern China and to provide more comprehensive and fundamental data for risk assessment of organochlorine contaminants (OCs) in environments. Samples were extracted and purified by the microwave-assisted extraction and solid-phase extraction system, respectively. PCBs and OCPs were analyzed by gas chromatograph-mass spectrometer. The concentrations of ΣPCBs and ΣOCPs ranged from 0.73 to 112.65 ng/g and 0.14 to 34.73 ng/g, respectively. PCBs in atmospheric particulates collected from Shijiazhuang City had the highest concentration, whereas OCP congeners were at the relatively low levels. However, the highest concentration of OCPs occurred in Yongning City. The principal component analysis indicated that the predominant compositions of PCBs in most of samples were tetrachlorobiphenyl (Tetra-CB), pentachlorobiphenyl (Penta-CB), hexachlorobiphenyl (Hexa-CB), and heptachlorbiphenyl (Hepta-CB), while hexachlorocyclohexanes (HCHs), DDTs, chlordanes, and endosulfans were the dominant components of OCPs, which was attributed to their application characteristics. OCs in those particles were further used to assess a potential cancer risk to humans via ingestion, dermal contact, and inhalation. Cancer risk was evaluated in airborne particles caused by PCBs and OCPs. TEQPCBs values suggested that the representative areas were subject to different pollution degrees. However, the pollution of OCPs in certain areas should be a concern due to 41.6% of the high risk, which could pose a potential risk to organisms. PMID:26139408

  12. Characterization of atmospheric particulate matter by diffusive gradient in thin film (DGT) technique

    Czech Academy of Sciences Publication Activity Database

    Gregušová, Michaela; Dočekal, Bohumil

    Brno : Ústav analytické chemie AV ČR, v. v. i, 2012 - (Foret, F.; Křenková, J.; Guttman, A.; Klepárník, K.; Boček, P.), s. 331-332 ISBN 978-80-904959-1-3. [CECE 2012. International Interdisciplinary Meeting on Bioanalysis /9./. Brno (CZ), 01.11.2012-02.11.2012] R&D Projects: GA ČR GAP503/10/2002; GA ČR(CZ) GAP503/11/2315; GA ČR(CZ) GBP503/12/G147 Institutional support: RVO:68081715 Keywords : DGT * particulate matter * metals Subject RIV: CB - Analytical Chemistry, Separation http://hdl.handle.net/11104/0215430

  13. Large-scale atmospheric circulation and local particulate matter concentrations in Bavaria - from current observations to future projections

    Science.gov (United States)

    Beck, Christoph; Weitnauer, Claudia; Brosy, Caroline; Hald, Cornelius; Lochbihler, Kai; Siegmund, Stefan; Jacobeit, Jucundus

    2016-04-01

    Particulate matter with an aerodynamic diameter of 10 μm or less (PM10) may have distinct adverse effects on human health. Spatial and temporal variations in PM10 concentrations reflect local emission rates, but are as well influenced by the local and synoptic-scale atmospheric conditions. Against this background, it can be furthermore argued that potential future climate change and associated variations in large-scale atmospheric circulation and local meteorological parameters will probably provoke corresponding changes in future PM10 concentration levels. The DFG-funded research project „Particulate matter and climate change in Bavaria" aimed at establishing quantitative relationships between daily and monthly PM10 indices at different Bavarian urban stations and the corresponding large-scale atmospheric circulation as well as local meteorological conditions. To this end, several statistical downscaling approaches have been developed for the period 1980 to 2011. PM10 data from 19 stations from the air quality monitoring network (LÜB) of the Bavarian Environmental Agency (LfU) have been utilized as predictands. Large-scale atmospheric gridded data from the NCEP/NCAR reanalysis data base and local meteorological observational data provided by the German Meteorological Service (DWD) served as predictors. The downscaling approaches encompass the synoptic downscaling of daily PM10 concentrations and several multivariate statistical models for the estimation of daily and monthly PM10, i.e.monthly mean and number of days exceeding a certain PM10 concentration threshold. Both techniques utilize objective circulation type classifications, which have been optimized with respect to their synoptic skill for the target variable PM10. All downscaling approaches have been evaluated via cross validation using varying subintervals of the 1980-2011 period as calibration and validation periods respectively. The most suitable - in terms of model skill determined from cross

  14. Size distributions of polycyclic aromatic hydrocarbons in urban atmosphere: sorption mechanism and source contributions to respiratory deposition

    Science.gov (United States)

    Lv, Yan; Li, Xiang; Xu, Ting Ting; Cheng, Tian Tao; Yang, Xin; Chen, Jian Min; Iinuma, Yoshiteru; Herrmann, Hartmut

    2016-03-01

    In order to better understand the particle size distribution of polycyclic aromatic hydrocarbons (PAHs) and their source contribution to human respiratory system, size-resolved PAHs have been studied in ambient aerosols at a megacity Shanghai site during a 1-year period (2012-2013). The results showed the PAHs had a bimodal distribution with one mode peak in the fine-particle size range (0.4-2.1 µm) and another mode peak in the coarse-particle size range (3.3-9.0 µm). Along with the increase in ring number of PAHs, the intensity of the fine-mode peak increased, while the coarse-mode peak decreased. Plotting of log(PAH / PM) against log(Dp) showed that all slope values were above -1, suggesting that multiple mechanisms (adsorption and absorption) controlled the particle size distribution of PAHs. The total deposition flux of PAHs in the respiratory tract was calculated as being 8.8 ± 2.0 ng h-1. The highest lifetime cancer risk (LCR) was estimated at 1.5 × 10-6, which exceeded the unit risk of 10-6. The LCR values presented here were mainly influenced by accumulation mode PAHs which came from biomass burning (24 %), coal combustion (25 %), and vehicular emission (27 %). The present study provides us with a mechanistic understanding of the particle size distribution of PAHs and their transport in the human respiratory system, which can help develop better source control strategies.

  15. Application of radiocarbon analysis and receptor modeling to the source apportionment of PAHs (polycyclic aromatic hydrocarbons) in the atmosphere

    International Nuclear Information System (INIS)

    The radiocarbon tracer technique was used to demonstrate that polycyclic aromatic hydrocarbons (PAHs) can be used for quantitative receptor modeling of air pollution. Fine-particle samples were collected during December, 1985, in Albuquerque, NM. Motor vehicles (fossil) and residential wood combustion (RWC, modern) were the major PAH-sources. For each sample, the PAH-fraction was solvent-extracted, isolated by liquid chromatography, and analyzed by GC-FID and GC-MS. The PAH-fractions from sixteen samples were analyzed for 14C by Accelerator Mass Spectrometry. Radiocarbon data were used to calculate the relative RWC contribution (fRWC) for samples analyzed for 14C. Normalized concentrations of a prospective motor vehicle tracer, benzo(ghi)perylene (BGP) had a strong, negative correlation with fRWC. Normalized BGP concentrations were used to apportion sources for samples not analyzed for 14C. Multiple Linear Regression (MLR) vs. ADCS and BGP was used to estimate source profiles for use in Target Factor Analysis (TFA). Profiles predicted by TFA were used in Chemical Mass Balances (CMBs). For non-volatile, stable PAHs, agreement between observed and predicted concentrations was excellent. The worst fits were observed for the most volatile PAHs and for coronene. The total RWC contributions predicted by CMBs correlated well with the radiocarbon data

  16. Annual distribution of allergenic fungal spores in atmospheric particulate matter in the Eastern Mediterranean; a comparative study between ergosterol and quantitative PCR analysis

    OpenAIRE

    N. Lang-Yona; Dannemiller, K.; Yamamoto, N; N. Burshtein; Peccia, J; O. Yarden; Rudich, Y.

    2012-01-01

    Airborne fungal spores are an important fraction of atmospheric particulate matter and are major causative agents of allergenic and infectious diseases. Predicting the variability and species of allergy-causing fungal spores requires detailed and reliable methods for identification and quantification. There are diverse methods for their detection in the atmosphere and in the indoor environments; yet, it is important to optimize suitable methods for characterization of fungal spores in atmosph...

  17. Annual distribution of allergenic fungal spores in atmospheric particulate matter in the Eastern Mediterranean; a comparative study between ergosterol and quantitative PCR analysis

    OpenAIRE

    N. Lang-Yona; Dannemiller, K.; Yamamoto, N; N. Burshtein; Peccia, J; O. Yarden; Rudich, Y.

    2012-01-01

    Airborne fungal spores are an important fraction of atmospheric particulate matter and are major causative agents of allergenic and infectious diseases. Predicting the variability and species of allergy-causing fungal spores requires detailed and reliable methods for identification and quantification. There are diverse methods for their detection in the atmosphere and in the indoor environments; yet, it is important to optimize suitable methods for characterization of fungal...

  18. Annual distribution of allergenic fungal spores in atmospheric particulate matter in the eastern mediterranean; a comparative study between ergosterol and quantitative PCR analysis

    OpenAIRE

    N. Lang-Yona; Dannemiller, K.; Yamamoto, N; N. Burshtein; Peccia, J; O. Yarden; Rudich, Y.

    2011-01-01

    Airborne fungal spores are an important fraction of atmospheric particulate matter and are major causative agents of allergenic and infectious diseases. Predicting the variability and species of allergy-causing fungal spores requires detailed and reliable methods for identification and quantification. There are diverse methods for their detection in the atmosphere and in the indoor environments; yet, it is important to optimize suitable methods for characterization of fungal spores in atmosph...

  19. Determination of Vanadium, Tin and Mercury in Atmospheric Particulate Matter and Cement Dust Samples by Direct Current Plasma Atomic Emission Spectrometry.

    Science.gov (United States)

    Hindy, Kamal T.; And Others

    1992-01-01

    An atmospheric pollution study applies direct current plasma atomic emission spectrometry (DCP-AES) to samples of total suspended particulate matter collected in two industrial areas and one residential area, and cement dust collected near major cement factories. These samples were analyzed for vanadium, tin, and mercury. The results indicate the…

  20. Polycyclic aromatic hydrocarbons (PAHs) in the Mediterranean Sea: Atmospheric occurrence, deposition and decoupling with settling fluxes in the water column

    International Nuclear Information System (INIS)

    ∑30PAH gas phase concentrations (13–86 and 22–40 ng m−3 in the Mediterranean and Black Seas, respectively) dominated the atmospheric levels due to the high contribution of phenanthrene, dibenzothiophene and their alkylated derivates. The high variability of PAH atmospheric concentrations in the different sub-basins is due to several factors (i.e. air-mass trajectory, proximity to sources and losses by deposition). The ∑30PAH atmospheric deposition (dominated by low MW PAH net air–water diffusive fluxes) is estimated to be ∼3100 ton y−1 (Mediterranean) and ∼500 ton y−1 (Black Sea). Net volatilization for certain PAHs was estimated. Deposition fluxes (1–2 orders of magnitude higher than reported PAH settling fluxes in the water column) confirm an important depletion/sink of water column PAH in the photic zone, especially for low MW PAHs. Degradation processes in the water column may be responsible for this decoupling. Conversely, high MW PAHs dry deposition fluxes are similar to their settling fluxes. Highlights: ► First comprehensive assessment of atmospheric PAH levels and deposition across the Mediterranean Sea. ► PAH atmospheric concentrations are highly variable across the Mediterranean Sea. ► Mediterranean Sea open waters receive ∼3100 ton of PAHs each year from the atmosphere. ► Important depletion of low MW PAH water column concentrations in the photic zone. ► Degradation processes most likely responsible of the atmospheric deposition – settling fluxes decoupling. - Capsule: Mediterranean Sea open waters receive ∼3100 ton of PAHs each year from the atmosphere but only a small fraction of this input settle down in the water column due to degradation processes.

  1. Multicomponent mixed dopant optimization for rapid screening of polycyclic aromatic hydrocarbons using ultra high performance liquid chromatography coupled to atmospheric pressure photoionization high-resolution mass spectrometry

    KAUST Repository

    Sioud, Salim

    2012-05-04

    RATIONALE To enhance the ionization efficiencies in atmospheric pressure photoionization mass spectrometry a dopant with favorable ionization energy such as chlorobenzene is typically used. These dopants are typically toxic and difficult to mix with water-soluble organic solvents. In order to achieve a more efficient and less toxic dopant, a multicomponent mixed dopant was explored. METHODS A multicomponent mixed dopant for non-targeted rapid screening of polycyclic aromatic hydrocarbons (PAHs) was developed and optimized using ultra high performance liquid chromatography (UPLC) coupled to atmospheric pressure photoionization high-resolution mass spectrometry. Various single and multicomponent mixed dopants consisting of ethanol, chlorobenzene, bromobenzene, anisole and toluene were evaluated. RESULTS Fourteen out of eighteen PAHs were successfully separated and detected at low pg/μL levels within 5 min with high mass accuracy ≤4 ppm. The optimal mixed multicomponent dopant consisted of ethanol/chlorobenzene/bromobenzene/anisole (98.975:0.1:0.9:0.025, v/v %) and it improved the limit of detection (LOD) by 2- to 10-fold for the tested PAHs compared to those obtained with pure chlorobenzene. CONCLUSIONS A novel multicomponent dopant that contains 99% ethanol and 1% mixture of chlorobenzene, bromobenzene and anisole was found to be an effective dopant mixture to ionize PAHs. The developed UPLC multicomponent dopant assisted atmospheric pressure photoionization high-resolution mass spectrometry offered a rapid non targeted screening method for detecting the PAHs at low pg/;μL levels within a 5 min run time with high mass accuracy a;circ4 ppm. Copyright © 2012 John Wiley & Sons, Ltd.

  2. Ambient PAH concentrations - results of long-term measurements of polycyclic aromatic hydrocarbons in Bavaria. PAK-Immissionskonzentrationen - Ergebnisse mehrjaehriger Messungen polycyclischer aromatischer Kohlenwasserstoffe in Bayern

    Energy Technology Data Exchange (ETDEWEB)

    Muecke, W.; Steinmetzer, H.C.; Stumpp, J. (Bayerisches Staatsministerium fuer Landesentwicklung und Umweltfragen, Muenchen (Germany)); Baumeister, W.; Boneberg, R.; Vierle, O. (Bayerisches Landesamt fuer Umweltschutz, Muenchen (Germany))

    1991-05-01

    Suspended particulate analyses were conducted in representative residential areas over longer periods, and 14 selected polycyclic aromatic hydrocarbons (PAHs) analysed within this framework (in accordance with the VDI quideline 3875, Sheet 1). The results show that in urban agglomerations significant regional differences exist, as a function of the emission situation, in the levels of atmospheric pollution through particle-bound PAH. A reduction of the total pollution has been achieved in recent years though air pollution control measures. (BBR).

  3. Magnetic particles in atmospheric particulate matter collected at sites with different level of air pollution

    Czech Academy of Sciences Publication Activity Database

    Petrovský, Eduard; Zbořil, R.; Matys Grygar, Tomáš; Kotlík, B.; Novák, J.; Kapička, Aleš; Grison, Hana

    2013-01-01

    Roč. 57, č. 4 (2013), s. 755-770. ISSN 0039-3169 R&D Projects: GA ČR GAP210/10/0554 Institutional support: RVO:67985530 ; RVO:61388980 Keywords : magnetite * atmospheric dust * pollution * rock magnetism Subject RIV: DI - Air Pollution ; Quality Impact factor: 0.752, year: 2013

  4. Polycyclic aromatic hydrocarbons (PAHs) in atmospheric PM2.5 around 2013 Asian Youth Games period in Nanjing

    Science.gov (United States)

    Li, Xuxu; Kong, Shaofei; Yin, Yan; Li, Li; Yuan, Liang; Li, Qi; Xiao, Hui; Chen, Kui

    2016-06-01

    Eighteen polycyclic aromatic hydrocarbons (PAHs) in PM2.5 collected near the Nanjing Olympic Sports Center across the Asian Youth Games (AYG) period (from August 2 to August 28, 2013) were analyzed using GC-MS. Their levels, sources and health risks to human were discussed. Results showed that the total concentrations of PAHs in PM2.5 were 9.43, 7.21 and 8.83 ng m- 3 for pre- (August 3-15), during- (August 16-24) and post- (August 25-28) AYG periods, respectively. They were dominated by 5-ring and 6-ring PAHs. Total PAHs concentrations in PM2.5 during AYG period decreased by 24%, when compared with those for pre-AYG period. For combustion-derived PAHs and carcinogenic PAHs, they decreased by 26% and 21%, respectively. It implied that the pollution control measures implemented during the AYG can effectively reduce the emission of PAHs from various sources. The poor correlations between PAHs and meteorological parameters also favored that the variations of PAHs were raised by the changes of emission sources. Diagnostic ratios and principal component analysis revealed that vehicle emission and coal combustion were the predominant contributors, with minimal effects from biomass burning and petroleum. The health risks for human exposed to PAHs in PM2.5 were quantitatively assessed by BaP equivalent concentration (BaPeq) and the incremental lifetime cancer risk (ILCR). The estimated ILCR value of PAHs during the AYG periods decreased by 23% and 27% for children and adults when compared with those for the pre-AYG, respectively. It indicated that the pollution control measures reduced the risks of PAHs to sportsmen or human gathered around the Olympic Sport Center.

  5. Lead isotopic compositions of atmospheric suspended particulate matter in Nagoya City as measured by HR-ICP-MS

    International Nuclear Information System (INIS)

    Lead isotope ratios in atmospheric suspended particulate matter (SPM) collected in Nagoya City were measured by high resolution inductively coupled plasma mass spectrometry (HR-ICP-MS) after microwave-assisted acid digestion. Before analyzing SPM samples, the present method was evaluated by analyzing standard reference material (SRM 981) for common lead isotopic standard from NIST. The analytical results for 207Pb/206Pb and 208Pb/206Pb for SRM 981 were 0.9160±0.0006 and 2.136±0.003, respectively, which were almost coincident with the certified values of 0.91464±0.00033 and 2.1681±0.0008, respectively. The lead isotope ratios in SPM samples collected daily in Nagoya University were analyzed in order to elucidate their origins, and the results were compared with various kinds of ores. It was found that most SPM samples showed some mixed compositions of lead isotope ratios of lead ores from USA and Australia, which suggested utilization of large amount of lead ores imported from these two countries. On the other hand, some samples showed mixed compositions of lead ores from Asian continent, which might be resulted from the long-range transportation of atmospheric SPM from Asian continent to Japan. (author)

  6. 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.

  7. Trends in concentrations of atmospheric gaseous and particulate species in rural eastern Tennessee as related to primary emission reductions

    Science.gov (United States)

    Tanner, R. L.; Bairai, S. T.; Mueller, S. F.

    2015-09-01

    Air quality measurements at Look Rock, Tennessee - on the western edge of the Great Smoky Mountains National Park - were begun in 1980 and expanded during the 1980s to a National Park Service (NPS) IMPROVE network station. Measurements were expanded again by the Tennessee Valley Authority (TVA, 1999-2007) to examine the effects of electric generating unit (EGU) emission reductions of SO2 and NOx on air quality at the station. Analysis of temporal trends (1999-2013) has been conducted at the site in collaboration with activities related to the 2013 Southeast Atmosphere Study (SAS) at Look Rock and other southeastern US locations. Key findings from these trend studies include the observation that primary pollutant levels have consistently tracked emission reductions from EGUs and other primary sources in the region, but reductions in secondary pollutants such as particulate sulfate and, specifically, ozone have been smaller compared to reductions in primary emissions. Organic carbonaceous material (OM) remains a major contributor (30-40 % in the period 2009-2013) to fine particulate mass at the site, as confirmed by ACSM measurements at the site in 2013. A large portion (65-85 %) of carbon in OM derives from modern carbon sources based on 14C measurements. Important parameters affecting ozone levels, fine mass, and visibility also include the specific diurnal meteorology at this ridge-top site, its location in a predominantly mixed-deciduous forest, and the presence of primary sources of precursors at distances of 50-500 km from the site in all directions.

  8. Characterization and source identification of trace elements in airborne particulates at urban and suburban atmospheres of Tabriz, Iran.

    Science.gov (United States)

    Gholampour, Akbar; Nabizadeh, Ramin; Hassanvand, Mohammad Sadegh; Taghipour, Hasan; Rafee, Mohammad; Alizadeh, Zahra; Faridi, Sasan; Mahvi, Amir Hossein

    2016-01-01

    Concentration of particulate matter (PM10 and total suspended particulate (TSP)) and their elemental constituents were measured to identify the major sources of elements in urban and industrial suburban sites in Tabriz, Iran, from September 2012 to June 2013. TSP and PM10 samples were collected using high-volume samplers. Concentrations of 31 elements in aerosols and crustal soil were determined by ICPMS. The most abundant detected metals in the urban sampling sites were Al (217.5-4019.9 ng m(-3)), Fe (272.5-7658.0 ng m(-3)), Pt (4.7-1994.4 ng m(-3)), and P (13.6-2054.8 ng m(-3) (for TSP and Al (217.6-3687.3 ng m(-3)), Fe (197.1-3724.9 ng m(-3)), Pt (65.9-2054.5 ng m(-3)), and P (11.0-756.6 ng m(-3)( for PM10. In the suburban sampling site, the most abundant detected metals were Al (2083.0-9664.0 ng m(-3)), Fe (360.0-7221.5 ng m(-3)), P (229.4-870.5 ng m(-3)), and Ti (137.3-849.7 ng m(-3)) for TSP and Al (218.5-4179.6 ng m(-3)), Fe (106.3-2005.1 ng m(-3)), P (251.9-908.4 ng m(-3)), and Ba (10.6-584.9 ng m(-3)) for PM10. For the crustal soil, the most abundant detected elements included Al (60,088-60,694 ppm), Fe (19,886-20,474 ppm), Ti (894-3481 ppm), and Si (365-4246 ppm). Key emission sources were identified, and the concentrations contributed from individual sources were estimated. Enrichment factor (EF) explaining a preponderance of the variance in the data was applied to the datasets. EF calculations revealed that non-crustal trace elements were more enriched in the urban than suburban sampling sites. Results of the factor analysis on the elements showed that emissions from road traffic (involving oil and fuel combustions by vehicles, platinum group elements from vehicle exhaust, and resuspension of particulate matter from polluted soil) and construction dust from nearby construction sites and electricity generation plant were the major contributors of anthropogenic metals at ambient atmosphere in Tabriz. Results of this study elucidated the need for

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

    Science.gov (United States)

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

    2012-01-01

    We report on the development and application of an integrated set of analytical tools that enable accurate measurement of total, extractable, and, importantly, the oxidation state of vanadium in sub-milligram masses of environmental aerosols and solids. Through rigorous control of blanks, application of magnetic-sector-ICPMS, and miniaturization of the extraction/separation methods we have substantially improved upon published quantification limits. The study focused on the application of these methods to particulate matter (PM) emissions from diesel vehicles, both in baseline configuration without after-treatment and also equipped with advanced PM and NO(x) emission controls. Particle size-resolved vanadium speciation data were obtained from dynamometer samples containing total vanadium pools of only 0.2-2 ng and provide some of the first measurements of the oxidation state of vanadium in diesel vehicle PM emissions. The emission rates and the measured fraction of V(V) in PM from diesel engines running without exhaust after-treatment were both low (2-3 ng/mile and 13-16%, respectively). The V(IV) species was measured as the dominant vanadium species in diesel PM emissions. A significantly greater fraction of V(V) (76%) was measured in PM from the engine fitted with a prototype vanadium-based selective catalytic reductors (V-SCR) retrofit. The emission rate of V(V) determined for the V-SCR equipped vehicle (103 ng/mile) was 40-fold greater than that from the baseline vehicle. A clear contrast between the PM size-distributions of V(V) and V(IV) emissions was apparent, with the V(V) distribution characterized by a major single mode in the ultrafine (vanadium-containing fine-particle PM from the V-SCR identified V(2)O(5) as the dominant vanadium species. PMID:22050708

  10. Pollution of atmospheric air with toxic and radioactive particulate matter investigated by means of nuclear techniques

    International Nuclear Information System (INIS)

    The application of spectrometric methods of nuclear techniques to the investigations of atmospheric air pollution by toxic and radioactive elements and results of these investigations conducted in the highly industrialized and urbanized regions of Poland have been presented. The method of precipitation of the samples, the measurements and analysis of radiation spectra of alpha and gamma radiation emitted by isotopes present in the samples have been described. The concentrations of toxic metal dust in the air have been evaluated by neutron activation and X-ray fluorescence analysis. Appropriate methods of measurement, calibration of instrument and the discussion of results have been presented. The work presents the results of investigations performed in Siersza within the years 1973-1974 and in Warsaw in the period of 1975-1977, which have permitted to estimate the mean monthly values of concentration in the atmospheric air of the following radioisotopes: 7Be, 54Mn, 95Zr, 103Ru, 106Ru, 125Sb, 131I, 137Cs, 140Ba, 141Ce, 144Ce, 226Ra, Th-nat, U-nat and the following stable elements: Sc, Cr, Fe, Co, Zn, As, Se, Sb, W, Pb. The analysis of changes in concentration of each particular artificial radioisotope in the air for the region of Poland in connection with Chinese nuclear explosions have been given. On the basis of the performed environmental investigations the method of analysis of relations between the concentrations of particular elements present in the dust has been discussed. The applications of this method have been presented. The hazard to the population and the environment caused by the radioactive and toxic dust present in the atmospheric air has been estimated. (author)

  11. Nature and sources of particle associated polycyclic aromatic hydrocarbons (PAH) in the atmospheric environment of an urban area

    International Nuclear Information System (INIS)

    The total PAH associated to the airborne particulate matter (PM10) was apportioned by one receptor model based on positive matrix factorization (PMF) in an urban environment (Zaragoza city, Spain) during February 2010–January 2011. Four sources associated with coal combustion, gasoline, vehicular and stationary emissions were identified, allowing a good modelling of the total PAH (R2 = 0.99). A seasonal behaviour of the four factors was obtained with higher concentrations in the cold season. The NE direction was one of the predominant directions showing the negative impact of industrial parks, a paper factory and a highway located in that direction. Samples were classified according to hierarchical cluster analysis obtaining that, episodes with the most negative impact on human health (the highest lifetime cancer risk concentrations), were produced by a higher contribution of stationary and vehicular emissions in winter season favoured by high relative humidity, low temperature and low wind speed. -- Highlights: ► PMF receptor model apportioned four sources associated to the total PAH in Zaragoza. ► The sources were: vehicular, coal combustion, gasoline and stationary emissions. ► Samples were additionally classified according to hierarchical cluster analysis. ► The stationary and vehicular emissions factors showed higher risk for human health. ► Low temperature, wind speed and high relative humidity favoured this negative impact. -- Episodes with the most negative impact on human health regarding PAH were produced by a higher contribution of stationary and vehicular emissions in winter season

  12. Spatio-temporal variations and influencing factors of polycyclic aromatic hydrocarbons in atmospheric bulk deposition along a plain-mountain transect in western China

    Science.gov (United States)

    Xing, Xinli; Zhang, Yuan; Yang, Dan; Zhang, Jiaquan; Chen, Wei; Wu, Chenxi; Liu, Hongxia; Qi, Shihua

    2016-08-01

    Ten atmospheric bulk deposition (the sum of wet and dry deposition) samplers for polycyclic aromatic hydrocarbons (PAHs) were deployed at a plain-mountain transect (namely PMT transect, from Daying to Qingping) in Chengdu Plain, West China from June 2007 to June 2008 in four consecutive seasons (about every three months). The bulk deposition fluxes of ∑15-PAHs ranged from 169.19 μg m-2 yr-1 to 978.58 μg m-2 yr-1 with geometric mean of 354.22 μg m-2 yr-1. The most prevalent PAHs were 4-ring (39.65%) and 3-ring (35.56%) PAHs. The flux values were comparable to those in rural areas. Higher fluxes of total PAHs were observed in the middle of PMT transect (SL, YX and JY, which were more urbanized than other sites). The seasonal deposition fluxes in the sampling profile indicated seasonality of the contaminant source was an important factor in controlling deposition fluxes. PAHs bulk deposition was negatively correlated with meteorological parameters (temperature, wind speed, humidity, and precipitation). No significant correlations between soil concentrations and atmospheric deposition were found along this transect. PAHs in soil samples had combined sources of coal, wood and petroleum combustion, while a simple source of coal, wood and grass combustion for bulk deposition. There were significant positive correlation relationship (p Mountain cold trap effect existed in this transect where the altitude was higher than 1000 m. Long-range transport had an impact on the bulk deposition in summer. And this transect was a source to Tibetan only in summer. The forward trajectory analysis showed most air masses did not undergo long-range transport due to the blocking effect of surrounding mountains. Only a few air masses (<10%) arrived at the eastern and northern region of China or farther regions via long-range transport.

  13. A computational study of particulate emissions from an open pit quarry under neutral atmospheric conditions

    Science.gov (United States)

    Silvester, S. A.; Lowndes, I. S.; Hargreaves, D. M.

    2009-12-01

    The extraction of minerals from surface mines and quarries can produce significant fugitive dust emissions as a result of site activities such as blasting, road haulage, loading, crushing and stockpiling. If uncontrolled, these emissions can present serious environmental, health, safety and operational issues impacting both site personnel and the wider community. The dispersion of pollutant emissions within the atmosphere is principally determined by the background wind systems characterized by the atmospheric boundary layer (ABL). This paper presents an overview of the construction and solution of a computational fluid dynamics (CFD) model to replicate the development of the internal ventilation regime within a surface quarry excavation due to the presence of a neutral ABL above this excavation. This model was then used to study the dispersion and deposition of fugitive mineral dust particles generated during rock blasting operations. The paths of the mineral particles were modelled using Lagrangian particle tracking. Particles of four size fractions were released from five blast locations for eight different wind directions. The study concluded that dependent on the location of the bench blast within the quarry and the direction of the wind, a mass fraction of between 0.3 and 0.6 of the emitted mineral particles was retained within the quarry. The retention was largest when the distance from the blast location to the downwind pit boundary was greatest.

  14. The sources and characteristics of atmospheric particulates during the wet and dry seasons in Hong Kong

    Science.gov (United States)

    Zheng, Mei

    Air pollution is a serious problem in Hong Kong due to the very high density of diesel powered engines and population as well as the geographical location, which places it under the significant influence of the Asian monsoon with the SW summer monsoon bringing clean oceanic aerosols and the NE winter monsoon bringing polluted continental emissions. To better characterize and obtain a picture of aerosol sources and transport, various techniques, including organic and inorganic tracers, SEM (Scanning Electron Microscope) micrographs, and lead isotopes in TSP (total suspended particulates) and size-fractionated aerosols, were applied in this study. The concentration and composition of aerosols in Hong Kong were significantly influenced by the large-scale meteorological patterns. In the wet season, lower levels were possibly due to greater precipitation, better dispersion, and significant contributions from coarse particles from the sea. Higher concentrations of crustal, flyash, pollution, and plant- wax materials were observed in the dry season. Examining chemical species in different sizes indicated the change of aerosol sources from the local sources in Hong Kong in the wet season to more aggregated materials in the transition period, and to stronger pollution emissions from the Asian continent in the dry season. Conventional factor analysis and chemical mass balance methods identified the sources of Hong Kong aerosols as marine, crustal, oil burning, coal, and incineration. The contributions from pollution and loess increased in the dry season. Oil burning was a stable factor and persisted through the wet and dry seasons, indicating that it was mainly from local sources. The majority of the mass of fine particle pollution elements such as Pb, Sb, and V was removed by wet scavenging, while dry and wet deposition were important for the coarser marine and crustal elements. Particle size as well as meteorological conditions can affect deposition velocities and dry

  15. Secondary brown carbon - Formation of light-absorbing compounds in atmospheric particulates from selected dicarbonyls and amines

    Science.gov (United States)

    Kampf, Christopher; Filippi, Alexander; Hoffmann, Thorsten

    2015-04-01

    One of the main open questions regarding organic compounds in atmospheric chemistry today is related to the formation of optically-active compounds and the occurrence of so called brown carbon (Andreae and Gelencsér, 2006). While organic compounds in ambient fine particles for decades have been assumed to not absorb solar radiation, thus resulting in a net cooling effect on climate (IPCC, 2007), it is now generally accepted that a continuum of light-absorbing carbonaceous species is present in fine aerosols (Pöschl, 2003). In this study, light-absorbing compounds from reactions between dicarbonyl compounds, i.e., glyoxal, methylglyoxal, acetylacetone, 2,3-butanedione, 2,5-hexanedione, and glutaraldehyde, and amine species, i.e., ammonia and glycine, were investigated at atmospherically relevant concentrations in bulk solution experiments mimicking atmospheric particulates. Product analyses were performed using UV/Vis spectrophotometry and (ultra) high performance liquid chromatography coupled to diode array detection and ion trap mass spectrometry (HPLC-DAD-ESI-MS/MS), as well as ultra-high resolution (Orbitrap) mass spectrometry (UHPLC-ESI-HRMS/MS). We demonstrate that light-absorbing compounds are formed from a variety of atmospherically relevant dicarbonyls via particle phase reactions with amine nucleophiles. Single dicarbonyl and mixed dicarbonyl experiments were performed and products were analyzed. The reaction products are suggested to be cyclic nitrogen containing compounds such as imidazoles or dihydropyridines as well as open chain compounds resulting from aldol condensation reactions. Further, the reactive turnover was found to be higher at increasing pH values. The aforementioned processes may be of higher relevance in regions with high aerosol pH, e.g., resulting from high ammonia emissions as for example in northern India (Clarisse et al., 2009). References Andreae, M.O., and Gelencsér, A. (2006): Black carbon or brown carbon? The nature of light

  16. LIDAR vertical profiles over the Oil Sands Region: an important tool in understanding atmospheric particulate matter transport, mixing and transformation

    Science.gov (United States)

    Strawbridge, K. B.

    2013-12-01

    LIDAR technology is an excellent tool to probe the complex vertical structure of the atmosphere at high spatial and temporal resolution. This provides the critical vertical context for the interpretation of ground-based chemistry measurements, airborne measurements and model verification and validation. In recent years, Environment Canada has designed an autonomous aerosol LIDAR system that can be deployed to remote areas such as the oil sands. Currently two autonomous LIDAR systems are making measurements in the oil sands region, one since December, 2012 and the other since July, 2013. The LIDAR transmitter emits two wavelengths (1064nm and 532nm) and the detector assembly collects four channels (1064nm backscatter, 532nm backscatter and 532nm depolarization, 607 nm nitrogen channel). Aerosol profiles from near ground to 20 km are collected every 10-60 s providing sufficient resolution to probe atmospheric dynamics, mixing and transport. The depolarization channel provides key information in identifying and discriminating the various aerosol layers aloft such as dust, forest fire plumes, industrial plume sources or ice crystals. The vertical resolution of the LIDAR can determine whether industrial plumes remain aloft or mix down to the surface and also provide estimates as to the concentration of the particulate at various altitudes. It operates 24 hours a day, seven days a week except during precipitation events. The system is operated remotely and the data are updated every hour to a website to allow near real-time capability. An intensive measurement campaign will be carried out in August and September of 2013 and will provide coincident airborne and ground-based measurements for the two LIDAR systems. The first results from this field study will be presented as well as some statistics on the frequency and evolution of plume events that were detected by the LIDARs.

  17. Thermodynamics of the formation of atmospheric organic particulate matter by accretion reactions—Part 1: aldehydes and ketones

    Science.gov (United States)

    Barsanti, Kelley C.; Pankow, James F.

    The term "accretion reactions" is introduced here to refer to the large collection of reactions by which atmospheric organic molecules can add mass, especially as by combination with other organic molecules. A general thermodynamic approach is developed for evaluating the tendency of atmospheric constituents (e.g., C 10 aldehydes) to undergo accretion reactions (e.g., dimerization) and thereby form less volatile molecules (e.g., aldol condensation products) that may subsequently condense and so contribute to the levels of organic particulate matter (OPM) observed in the atmosphere. As an example, gaseous compounds A and B may contribute to OPM formation by the net overall reaction A g+B g=C liq. This reaction may occur according to any of three kinetic schemes. Scheme I: (1) A g+B g=C g (accretion in the gas phase): then (2) C g=C liq (condensation of the accretion product); Scheme II: (1) B g=B liq (condensation of B); then (2) A g+B liq=C liq (heterogeneous accretion reaction of gaseous A with condensed B); or Scheme III: (1) A g+B g=A liq+B liq (condensation of A and B); then (2) A liq+B liq=C liq (accretion of A with B within the PM phase). For all three schemes, the net overall reaction remains A g+B g=C liq. The overall thermodynamic tendency of the net reaction remains the same regardless of the actual predominating kinetic mechanism. If an accretion reaction between two atmospheric components is to produce significant new OPM, appreciable amounts of the product C must form, and the vapor pressure of C must be relatively low so that a significant proportion of C can condense into the multicomponent liquid OPM phase. This study considers the thermodynamics of accretion reactions of atmospheric aldehydes including: (a) hydration, polymerization (i.e., oligomer formation), hemiacetal/acetal formation; and (b) aldol condensation. It was concluded regarding OPM formation that: (1) the reactions in the first group are not thermodynamically favored, either in the

  18. Spatio-temporal variations and influencing factors of polycyclic aromatic hydrocarbons in atmospheric bulk deposition along a plain-mountain transect in western China

    Science.gov (United States)

    Xing, Xinli; Zhang, Yuan; Yang, Dan; Zhang, Jiaquan; Chen, Wei; Wu, Chenxi; Liu, Hongxia; Qi, Shihua

    2016-08-01

    Ten atmospheric bulk deposition (the sum of wet and dry deposition) samplers for polycyclic aromatic hydrocarbons (PAHs) were deployed at a plain-mountain transect (namely PMT transect, from Daying to Qingping) in Chengdu Plain, West China from June 2007 to June 2008 in four consecutive seasons (about every three months). The bulk deposition fluxes of ∑15-PAHs ranged from 169.19 μg m-2 yr-1 to 978.58 μg m-2 yr-1 with geometric mean of 354.22 μg m-2 yr-1. The most prevalent PAHs were 4-ring (39.65%) and 3-ring (35.56%) PAHs. The flux values were comparable to those in rural areas. Higher fluxes of total PAHs were observed in the middle of PMT transect (SL, YX and JY, which were more urbanized than other sites). The seasonal deposition fluxes in the sampling profile indicated seasonality of the contaminant source was an important factor in controlling deposition fluxes. PAHs bulk deposition was negatively correlated with meteorological parameters (temperature, wind speed, humidity, and precipitation). No significant correlations between soil concentrations and atmospheric deposition were found along this transect. PAHs in soil samples had combined sources of coal, wood and petroleum combustion, while a simple source of coal, wood and grass combustion for bulk deposition. There were significant positive correlation relationship (p atmospheric bulk deposition and local PAHs emission, with biomass burning as the major contribution to the total emission of PAHs. This transect acts as an important PAHs source rather than being a sink according to the ratio of deposition/emission. Mountain cold trap effect existed in this transect where the altitude was higher than 1000 m. Long-range transport had an impact on the bulk deposition in summer. And this transect was a source to Tibetan only in summer. The forward trajectory analysis showed most air masses did not undergo long-range transport due to the blocking effect of surrounding mountains. Only a few air masses (<10

  19. On the Fractal Mechanism of Interrelation Between the Genesis, Size and Composition of Atmospheric Particulate Matters in Different Regions of the Earth

    CERN Document Server

    Rusov, Vitaliy D; Jacimovic, Radojko R; Pavlovich, Vladimir N; Bondarchuk, Yuriy A; Vaschenko, Vladimir N; Zelentsova, Tatiana N; Beglaryan, Margarita E; Linnik, Elena P; Smolyar, Vladimir P; Kosenko, Sergey I; Gudyma, Alla A

    2011-01-01

    Experimental data from the National Air Surveillance Network of Japan from 1974 to 1996 and from independent measurements performed simultaneously in the regions of Ljubljana (Slovenia), Odessa (Ukraine) and the Ukrainian "Academician Vernadsky" Antarctic station (64{\\deg}15'W; 65{\\deg}15'S), where the air elemental composition was determined by the standard method of atmospheric particulate matter (PM) collection on nucleopore filters and subsequent neutron activation analysis, were analyzed. Comparative analysis of different pairs of atmospheric PM element concentration data sets, measured in different regions of the Earth, revealed a stable linear (on a logarithmic scale) correlation, showing a power law increase of every atmospheric PM element mass and simultaneously the cause of this increase - fractal nature of atmospheric PM genesis. Within the framework of multifractal geometry we show that the mass (volume) distribution of atmospheric PM elemental components is a log normal distribution, which on a l...

  20. A simplified method for levoglucosan quantification in wintertime atmospheric particulate matter by high performance anion-exchange chromatography coupled with pulsed amperometric detection

    OpenAIRE

    Piazzalunga, A.; P. Fermo; Bernardoni, V.; VECCHI, R; Valli, G.; M. Gregorio

    2010-01-01

    Levoglucosan, a tracer for the assessment of the biomass burning contribution to atmospheric particulate matter (PM) concentrations, was determined by means of high-performance anion-exchange chromatography (HPAEC) with pulsed amperometric detection (PAD). In this work we propose a modification in the instrumental set-up aiming at an improvement in the detector response by adding NaOH after chromatographic separation to increase the pH. The comparison betwe...

  1. Distribution of atmospheric particulate matter (PM) in rural field, rural village and urban areas of northern China

    International Nuclear Information System (INIS)

    Atmospheric PM10 were measured for 12 months at 18 sites along a 2500 km profile across northern China. Annual mean PM10 concentrations in urban, rural village, and rural field sites were 180 ± 171, 182 ± 154, and 128 ± 89 μg/m3, respectively. The similarities in PM10 concentrations between urban and rural village sites suggest that strong localized emissions and severe contamination in rural residential areas are derived from solid fuels combustion in households. High PM10 concentrations in Wuwei and Taiyuan were caused by either sandstorms or industrial activities. Relatively low PM10 concentrations were observed in coastal areas of Dalian and Yantai. Particulate air pollution was much higher in winter and spring than in summer and fall. Multiple regression analysis indicates that 35% of the total variance can be attributed to sandstorms, precipitation and residential energy consumption. Over 40% of the measurements in both urban and rural village areas exceeded the national ambient air quality standard. Highlights: • Spatial distribution of PM10 concentrations in northern China was investigated. • High levels of PM10 in rural villages were caused by solid fuel emission. • A strong seasonality with high levels of PM10 in spring and winter was observed. • Influence of sandstorm, energy consumption, and precipitation were evaluated. • Over 40% of the measurements exceeded the national ambient air quality standard. -- PM10 concentrations in rural villages of China were comparable with those in the cities, indicating severe air pollution in the rural villages caused by coal and biofuel combustion

  2. Performance testing of cross flow heat exchanger operating in the atmosphere of flue gas particulate with vapor condensation

    Directory of Open Access Journals (Sweden)

    Nuntaphan, A.

    2006-05-01

    Full Text Available Performance testing of a cross flow heat exchanger operating under the atmosphere of flue gas particulate from combustion was carried out in this work. This heat exchanger exchanges heat between flue gas from the fuel oil combustion and cold water. The heat exchanger is composed of a spiral finned tube bank having 3 rows and 8 tubes per row with a staggered arrangement. The fin spacings considered are 2.85 and 6.10 mm. The theories of thermodynamics and heat transfer are used for analyzing the performance of this system.In this experiment, the flue gas temperature of 200ºC from combustion having 0.35 kg/s mass flow rate flows along outside surface of the heat exchanger and transfers heat to the 25ºC cooling water having 0.15 kg/s mass flow rate flowing in the tube side. Each experiment uses 750 hr for testing. During the testing, part of flue gas condenses on the heat transfer surface.From the experiment, it was found that the heat transfer rate of both heat exchangers tended to decrease with time while the airside pressure drop increased. These results come from the fouling on the heat transfer surface. Moreover, it is found that the heat exchanger having 2.85 mm fin spacing has an approximately 4 times higher fouling resistance than that of the 6.10 mm fin spacing.In this work a model for calculating the fouling resistance is also developed as a the function of time. The model is developed from that of Kern and Seaton and the mean deviation of the model is 0.789.

  3. Development of methods to examine the effects of atmospheric particulate matter (PM) on human peripheral blood leukocytes

    Science.gov (United States)

    Zussman, Lisa Ann

    In vitro methods to study the effect of atmospheric particulate matter (PM) on leukocyte function using human peripheral blood were developed. These methods were demonstrated using the blood of 1-5 individuals and National Institute of Standards and Technology (NIST) urban PM #1648, diesel PM #1650, silica PM, and a locally collected PM sample (New Jersey PM10). For the blood samples analyzed in this study NIST urban PM and New Jersey PM10 treatment mediated the release of granule contents from peripheral blood leukocytes and induced structural changes associated with degranulation. Flow cytometry revealed PM-induced changes in phagocytosis and cell structure associated with degranulation. Transmission electron microscopy confirmed NIST urban PM-induced cell structure changes were associated with PM internalization. Colorametric and electrophoretic methods showed no PM-induced release of primary granules and a slight PM-induced release of secondary granules associated with only NIST urban PM. Enzyme Immunosorbent Assays detected increased histamine release from basophils treated with NIST urban PM, a locally collected PM, and the soluble and insoluble components of these particles. NIST urban PM was found to be a potent inducer of histamine release in 4 out of 6 individuals tested. Fractionation studies revealed that soluble (aqueous) and insoluble fractions of NIST urban PM contain histamine-releasing activity. This was also demonstrated for the New Jersey PM10 sample for which the soluble fraction exhibited the most activity. Complementary studies with inhibitors of IgE-mediated histamine release conducted on one test subject suggest that PM-induced histamine release was partially mediated by IgE. A new hypothesis has been formed, suggesting that particle toxicity is related to PM-induced histamine release. Due to the bioactive nature of histamine and its association with many cardiopulmonary responses, the PM- mediated release of histamine should be investigated

  4. 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.

  5. Assessing the influence of the North Atlantic Oscillation on the European atmospheric composition from a climatic perspective: a case study for polycyclic aromatic hydrocarbons

    Science.gov (United States)

    Jimenez-Guerrero, Pedro; Jerez, Sonia; Ratola, Nuno

    2014-05-01

    The North Atlantic Oscillation (NAO) controls a large amount of the European climate variability with asymmetric impacts in both time and space. These NAO-related impacts on the atmospheric fields are bound to influence the atmospheric composition, through both local processes and large-scale transport of air pollutants. The studies devoted to explore such an influence from a climatic perspective (long-term modeling) are few, and even less disentangling between local and large-scale settings. Therefore, the contribution of the local NAO-controlled processes on the climatology of air pollution levels is still hardly established. Hence, the objective of the present study is to assess the NAO fingerprint in terms of mean concentration of polycyclic aromatic hydrocarbons (PAHs, in this case benzo[a]pyrene, BaP) in a region covering the entire Mediterranean basin from the north of Africa to the north of Europe, focusing on the influence of the small scale processes. BaP is arguably the most studied PAH, and the reference for PAH air quality standards defined by the European Commission. To achieve this goal, we use a numerical simulation of the atmospheric chemical composition that spans from 1989 to 2010 and fixing the anthropogenic emissions, thus allowing to isolate the climatic variations in BaP. The chemistry transport model selected was CHIMERE and the domain considered has a spatial resolution of 0.2 degrees in the horizontal, which is about 25 km at the European latitudes considered, and eight vertical levels unevenly spaced up to 550 hPa. This resolution is higher than the commonly applied in climate runs. The simulation was designed to disregard the signals from the NAO impact on the long-range transport, using constant climatological boundary conditions for the pollutants concentrations. This allows the enhancement of our understanding regarding the role of the local underlying mechanisms as they are governed by the NAO. The results show impacts with

  6. Molecular view modeling of atmospheric organic particulate matter: Incorporating molecular structure and co-condensation of water

    Science.gov (United States)

    Pankow, James F.; Marks, Marguerite C.; Barsanti, Kelley C.; Mahmud, Abdullah; Asher, William E.; Li, Jingyi; Ying, Qi; Jathar, Shantanu H.; Kleeman, Michael J.

    2015-12-01

    Most urban and regional models used to predict levels of organic particulate matter (OPM) are based on fundamental equations for gas/particle partitioning, but make the highly simplifying, anonymized-view (AV) assumptions that OPM levels are not affected by either: a) the molecular characteristics of the condensing organic compounds (other than simple volatility); or b) co-condensation of water as driven by non-zero relative humidity (RH) values. The simplifying assumptions have allowed parameterized chamber results for formation of secondary organic aerosol (SOA) (e.g., "two-product" (2p) coefficients) to be incorporated in chemical transport models. However, a return towards a less simplistic (and more computationally demanding) molecular view (MV) is needed that acknowledges that atmospheric OPM is a mixture of organic compounds with differing polarities, water, and in some cases dissolved salts. The higher computational cost of MV modeling results from a need for iterative calculations of the composition-dependent gas/particle partition coefficient values. MV modeling of OPM that considered water uptake (but not dissolved salts) was carried out for the southeast United States for the period August 29 through September 7, 2006. Three model variants were used at three universities: CMAQ-RH-2p (at PSU), UCD/CIT-RH-2p (at UCD), and CMAQ-RH-MCM (at TAMU). With the first two, MV structural characteristics (carbon number and numbers of functional groups) were assigned to each of the 2p products used in CMAQv.4.7.1 such that resulting predicted Kp,i values matched those in CMAQv.4.7.1. When water uptake was allowed, most runs assumed that uptake occurred only into the SOA portion, and imposed immiscibility of SOA with primary organic aerosol (POA). (POA is often viewed as rather non-polar, while SOA is commonly viewed as moderately-to-rather polar. Some runs with UCD/CIT-RH-2p were used to investigate the effects of POA/SOA miscibility.) CMAQ-RH-MCM used MCM to

  7. Heterogeneous reactions of particulate matter-bound PAHs and NPAHs with NO3/N2O5, OH radicals, and O3 under simulated long-range atmospheric transport conditions: reactivity and mutagenicity.

    Science.gov (United States)

    Jariyasopit, Narumol; Zimmermann, Kathryn; Schrlau, Jill; Arey, Janet; Atkinson, Roger; Yu, Tian-Wei; Dashwood, Roderick H; Tao, Shu; Simonich, Staci L Massey

    2014-09-01

    The heterogeneous reactions of ambient particulate matter (PM)-bound polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs (NPAHs) with NO3/N2O5, OH radicals, and O3 were studied in a laboratory photochemical chamber. Ambient PM2.5 and PM10 samples were collected from Beijing, China, and Riverside, California, and exposed under simulated atmospheric long-range transport conditions for O3 and OH and NO3 radicals. Changes in the masses of 23 PAHs and 20 NPAHs, as well as the direct and indirect-acting mutagenicity of the PM (determined using the Salmonella mutagenicity assay with TA98 strain), were measured prior to and after exposure to NO3/N2O5, OH radicals, and O3. In general, O3 exposure resulted in the highest relative degradation of PM-bound PAHs with more than four rings (benzo[a]pyrene was degraded equally well by O3 and NO3/N2O5). However, NPAHs were most effectively formed during the Beijing PM exposure to NO3/N2O5. In ambient air, 2-nitrofluoranthene (2-NF) is formed from the gas-phase NO3 radical- and OH radical-initiated reactions of fluoranthene, and 2-nitropyrene (2-NP) is formed from the gas-phase OH radical-initiated reaction of pyrene. There was no formation of 2-NF or 2-NP in any of the heterogeneous exposures, suggesting that gas-phase formation of NPAHs did not play an important role during chamber exposures. Exposure of Beijing PM to NO3/N2O5 resulted in an increase in direct-acting mutagenic activity which was associated with the formation of mutagenic NPAHs. No NPAH formation was observed in any of the exposures of the Riverside PM. This was likely due to the accumulation of atmospheric degradation products from gas-phase reactions of volatile species onto the surface of PM collected in Riverside prior to exposure in the chamber, thus decreasing the availability of PAHs for reaction. PMID:25119270

  8. Chemical and biological characterization of urban particulate matter

    International Nuclear Information System (INIS)

    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)

  9. Seasonal and spatial variation of atmospheric particulate matter in a developing megacity, the Greater Cairo, Egypt Egipto

    Energy Technology Data Exchange (ETDEWEB)

    Zakey, A.S. [The Abdus Salam International Centre of Theoretical Physics (ICTP) Trieste (Italy)]. E-mail: azakey@ictp.it; Abdel-Wahab, M.M. [Cairo University, Department of Meteorology, Faculty of Science, Cairo (Egypt); Pettersson, J.B.C.; Gatari, M.J.; Hallquist, M. [Department of Chemistry, Atmospheric Science, Goeteborg University, Goeteborg (Sweden)

    2008-04-15

    As an example of a developing megacity the Greater Cairo (GC) area in Egypt has been evaluated with respect to atmospheric particulate matter (PM) and lead (Pb). Particulate matter was collected during 2001-2002 in the two size fractions PM{sub 2}.5 and PM{sub 1}0 at 17 sites representing different activities (industrial, urban, residential and background condition). The PM concentrations were generally high, with yearly average PM{sub 2}.5 and PM{sub 1}0 values of 85 {+-} 12 and 170 {+-} 25 {mu}g/m{sup -}3, respectively. On an annual scale, the high PM levels were due to many sources that included traffic, waste burning and wind blown dust particles emitted from the desert outside GC and the Moqattam hill inside GC. On a seasonal scale, the PM concentrations were highest in the industrial sector during spring, the dusty season, due to the combined effect of dust storm events and anthropogenic emissions over GC. The lowest seasonal concentrations were recorded in the summer season at the background sites. There was a marked increase in PM levels during the period October to December due to burning of waste from harvested rice in the agriculture area in the Nile Delta (north of Cairo). The highest PM{sub 2}.5/PM{sub 1}0 ratio was recorded in the urban sector (0.59) while the lowest ratio was recorded in the residential sector (0.32). The PM{sub 2}.5 and PM{sub 1}0 samples were also analyzed for Pb in order to address the influence of different emission sources. The monthly average concentrations of Pb in both PM{sub 2}.5 (Pb{sub 2}.5) and PM{sub 1}0 (Pb{sub 1}0) varied between 0.4 and 1.8 {+-} {mu}g m{sup -}3 at the non industrial sites. The concentrations were significantly higher in the industrial areas, where concentration up to a maximum of 16 {+-} g m{sup -}3 could be observed. Both the high lead and PM concentrations measured are contributing to local environmental pollution. GC is subjected to high concentrations of particulates most of the year. There is no

  10. Atmospheric concentrations and air–soil gas exchange of polycyclic aromatic hydrocarbons (PAHs) in remote, rural village and urban areas of Beijing–Tianjin region, North China

    OpenAIRE

    Wang, Wentao; Simonich, Staci; Giri, Basant; Chang, Ying; Zhang, Yuguang; Jia, Yuling; Tao, Shu; Wang, Rong; Wang, Bin; Li, Wei; Cao, Jun; LU, XIAOXIA

    2011-01-01

    Forty passive air samplers were deployed to study the occurrence of gas and particulate phase PAHs in remote, rural village and urban areas of Beijing–Tianjin region, North China for four seasons (spring, summer, fall and winter) from 2007 to 2008. The influence of emissions on the spatial distribution pattern of air PAH concentrations was addressed. In addition, the air–soil gas exchange of PAHs was studied using fugacity calculations. The median gaseous and particulate phase PAH concentrati...

  11. Atmospheric mercury and fine particulate matter in coastal New England: implications for mercury and trace element sources in the northeastern United States

    Science.gov (United States)

    Kolker, Allan; Engle, Mark A.; Peucker-Ehrenbrink, Bernhard; Geboy, Nicholas J.; Krabbenhotft, David P. Krabbenhoft; Bothner, Michael H. Bothner; Tate, Michael T.

    2013-01-01

    Intensive sampling of ambient atmospheric fine particulate matter was conducted at Woods Hole, Massachusetts over a four-month period from 3 April to 29 July, 2008, in conjunction with year-long deployment of the USGS Mobile Mercury Lab. Results were obtained for trace elements in fine particulate matter concurrently with determination of ambient atmospheric mercury speciation and concentrations of ancillary gasses (SO2, NOx, and O3). For particulate matter, trace element enrichment factors greater than 10 relative to crustal background values were found for As, Bi, Cd, Cu, Hg, Pb, Sb, V, and Zn, indicating contribution of these elements by anthropogenic sources. For other elements, enrichments are consistent with natural marine (Na, Ca, Mg, Sr) or crustal (Ba, Ce, Co, Cs, Fe, Ga, La, Rb, Sc, Th, Ti, U, Y) sources, respectively. Positive matrix factorization was used together with concentration weighted air-mass back trajectories to better define element sources and their locations. Our analysis, based on events exhibiting the 10% highest PM2.5 contributions for each source category, identifies coal-fired power stations concentrated in the U.S. Ohio Valley, metal smelting in eastern Canada, and marine and crustal sources showing surprisingly similar back trajectories, at times each sampling Atlantic coastal airsheds. This pattern is consistent with contribution of Saharan dust by a summer maximum at the latitude of Florida and northward transport up the Atlantic Coast by clockwise circulation of the summer Bermuda High. Results for mercury speciation show diurnal production of RGM by photochemical oxidation of Hg° in a marine environment, and periodic traverse of the study area by correlated RGM-SO2(NOx) plumes, indicative of coal combustion sources.

  12. Influence of Biomass Burning on Temporal and Diurnal Variations of Acidic Gases, Particulate Nitrate, and Sulfate in a Tropical Urban Atmosphere

    Directory of Open Access Journals (Sweden)

    Sailesh N. Behera

    2014-01-01

    Full Text Available The present study investigated the temporal and diurnal distributions of atmospheric acidic gases (sulphur dioxide (SO2, nitrous acid (HONO, and nitric acid (HNO3 and those of particulate nitrate (NO3- and sulfate (SO42- through a comprehensive field campaign during the largest smoke haze episode in Singapore, a representative country in Southeast Asia (SEA. To identify the atmospheric behavior of these pollutants during the smoke haze period, the data generated from the measurement campaign were divided into three distinct periods: prehaze, during haze, and posthaze periods. The 24 hr average data indicated that ambient SO2, HONO, and HNO3 during the smoke haze episodes increased by a factor ranging from 1.2 to 2.6 compared to those during the prehaze and posthaze periods. Similarly, in the case of particulates SO42- and NO3-, the factor ranged from 2.3 to 4.2. Backward air trajectories were constructed and used to find the sources of biomass burning to the recurring smoke haze in this region. The air trajectory analysis showed that the smoke haze episodes experienced in Singapore were influenced by transboundary air pollution, caused by severe biomass burning events in the islands of Indonesia.

  13. Design, testing and demonstration of a small unmanned aircraft system (sUAS) and payload for measuring wind speed and particulate matter in the atmospheric boundary layer

    Science.gov (United States)

    Riddell, Kevin Donald Alexander

    The atmospheric boundary layer (ABL) is the layer of air directly influenced by the Earth's surface and is the layer of the atmosphere most important to humans as this is the air we live in. Methods for measuring the properties of the ABL include three general approaches: satellite based, ground based and airborne. A major research challenge is that many contemporary methods provide a restricted spatial resolution or coverage of variations of ABL properties such as how wind speed varies across a landscape with complex topography. To enhance our capacity to measure the properties of the ABL, this thesis presents a new technique that involves a small unmanned aircraft system (sUAS) equipped with a customized payload for measuring wind speed and particulate matter. The research presented herein outlines two key phases in establishing the proof of concept of the payload and its integration on the sUAS: (1) design and testing and (2) field demonstration. The first project focuses on measuring wind speed, which has been measured with fixed wing sUASs in previous research. but not with a helicopter sUAS. The second project focuses on the measurement of particulate matter, which is a major air pollutant typically measured with ground-based sensors. Results from both proof of concept projects suggest that ABL research could benefit from the proposed techniques. .

  14. Trends in Concentrations of Atmospheric Gaseous and Particulate Species at the Look Rock, TN NCORE Air Quality Station and Their Relation to Primary Emissions Reductions

    Science.gov (United States)

    Tanner, R. L.; Mueller, S. F.; Bairai, S. T.

    2013-12-01

    Air quality parameters, measured at Look Rock, TN, since 1980, were expanded by National Park Service (NPS) as an IMPROVE network station and again in 1999-2007 by Tennessee Valley Authority as part of efforts to determine the effects of reductions in EGU emissions of sulfur and nitrogen oxides on air quality at the site. Designated as a non-urban, NCORE-equivalent station in 2010, routine continuous monitoring of aerosol mass, sulfate, and black carbon, and primary and secondary gases at the site as well as additional measurements during a series of intensive research studies at the site have produced an extensive body to air quality data on background levels of species relevant to air quality standards (NAAQS) for ozone and fine particulate matter which is unique comprehensive for a high-altitude site in the southeastern U.S.A. Analysis of the temporal trends in these data (1999-present)is being conducted in conjunction with and support of 2013 Southern Atmosphere Studies at Look Rock and other southeastern U.S. locations. Key findings from analysis of temporal trends at Look Rock include the observation that primary pollutant levels have consistently tracked the emissions reductions from EGUs and other primary sources in the region, but reductions in secondary pollutants such as particulate sulfate and ozone have been less than proportional. Organic carbonaceous material (OM) remains a major contributor to fine particulate mass at the site, and a large portion (65-85%) of OM derives from modern carbon, based on 14C measurements. Important parameters affecting fine mass and ozone levels also include the specific diurnal meteorology at this ridge-top site, its location in a largely mixed-deciduous forest, and the presence of primary sources of precursors at distances of 50-500 km from the site in all directions.

  15. Seasonal dynamics of coarse atmospheric particulate matter between 2.5 μm and 80 μm in Beijing and the impact of 2008 Olympic Games

    Science.gov (United States)

    Norra, Stefan; Yu, Yang; Dietze, Volker; Schleicher, Nina; Fricker, Mathieu; Kaminski, Uwe; Chen, Yuan; Stüben, Doris; Cen, Kuang

    2016-01-01

    Beijing is well known as a megacity facing severe atmospheric pollution problems. One very important kind of pollution is the high amount of particles in Beijing's atmosphere. Numerous studies investigated the dynamics of fine particles smaller 10 μm. Less information is available on the coarse particle fraction larger 10 μm, although geogenic dusts, which often are composed by those coarser particles, frequently affect the air quality in Beijing. Therefore, systematic sampling and analysis of size fractionated particulate matter between 2.5 and 80 μm was performed in Beijing from April 2005 till October 2009. Atmospheric particles were collected in the North-West of Beijing using a cost-effective passive sampling method called Sigma-2. Altogether, 200 weeks could be analysed and assessed. Concentrations and size distribution of atmospheric coarse particles were determined by automated microscopic single particle analysis. Seasonal variability of the total mass of different size fractions was identified as follows: spring > winter > autumn > summer. High concentrations of transparent mineral particles indicate the activity of geogenic sources in spring and winter time, due to asian dust events and resuspension of soil from local bare land during dry and windy periods. The percentage of opaque particle components differs seasonally with relatively high values in winter, confirming combustion of fossil fuels for heating purposes as a predominant pollution source in this season. The influence of meteorological conditions on concentrations and size distribution of atmospheric particulate matter between 2.5 and 80 μm is demonstrated for the whole sampling period. Lowest pollution by coarse aerosols occurred during the period of the 2008 Olympic Summer Games. A general trend of decreasing total coarse particle mass concentrations was observed. Due to frequently observed high total coarse particle mass concentrations of several 100 μg·m-³ it is strongly recommended

  16. Determination of water-soluble inorganic species in airborne atmospheric particulate matter in an Urban Area in Jordan

    International Nuclear Information System (INIS)

    Major water soluble cations and anions in inhalable (INP) and noninhalable (Nip) airbome particulate matter samples have been determined in an urban area of Amman city of Jordan during Winter, 1996 by ion chromatography. The total average level of F-, CI+, NO3+, SO42- and total suspended particles (Tsp) were 1.48, 3.84, 6.40, 45.85 and 221μg/m3, respectively. For cations, the total average levels were 25.42, 6.68, 4.06, 5.84, and 25.05 μg/m3 for Na+, NH4+, Mg2+, and Ca2+, respectively. This study show ss that the concentrations of FΛ, NO3Λ, SO42, Na+, K+, Mg2+, and Ca2+ in the INP fraction were significantly greater than in the Nip fraction while the CI+ and NH4+ levels are greater than in the Nip, In the same sampling site, it was found that the nitrate and sulfate concentrations in air particulate matter are significantly higher in winter, 1996 than in summer season, 1995. However, the levels of fluoride and chloride are greater in summer than in winter. (authors). 24 refs., 5 figs., 2 table

  17. Biotransformation of polycyclic aromatic hydrocarbons in marine polychaetes

    DEFF Research Database (Denmark)

    Jørgensen, Anne; Giessing, Anders; Rasmussen, Lene Juel;

    2008-01-01

    Deposit-feeding polychaetes constitute the dominant macrofauna in marine environments that tend to be depositional centers for organic matter and contaminants. Polychaetes are known to accumulate polycyclic aromatic hydrocarbons (PAHs) from both particulate and dissolved phases but less is known ...

  18. Pressurized liquid extraction technique for the analysis of pesticides, PCBs, PBDEs, OPEs, PAHs, alkanes, hopanes, and steranes in atmospheric particulate matter.

    Science.gov (United States)

    Clark, Adelaide E; Yoon, Subin; Sheesley, Rebecca J; Usenko, Sascha

    2015-10-01

    An analytical method has been developed for the pressurized liquid extraction (PLE) of a wide range of semi-volatile organic compounds (SVOCs) from atmospheric particulate matter. Approximately 130 SVOCs from eight compound classes were selected as molecular markers of (1) agricultural activity (30 current and historic-use pesticides), (2) industrial activity (18 PCBs), (3) consumer products and building materials (16 PBDEs, 11 OPEs), and (4) motor vehicle exhaust (22 PAHs, 16 alkanes, 9 hopanes, 8 steranes). Currently, there is no analytical method validated for the extraction of all eight compound classes in a single automated technique. The extraction efficiencies of varying solvents and solvent combinations at high temperatures and pressures were examined. Extracts were concentrated and analyzed by gas chromatography coupled with mass spectrometry. The optimized PLE method utilized methylene chloride:acetone (2:1 v/v) at 100 °C with three (5 min) static cycles, flush volume of 80%, and a 100 s N2 purge. Spike and recovery experiments (n=7) provided average percent recoveries for pesticides, PCBs, PBDEs, OPEs, PAHs, alkanes, hopanes, and steranes of 88.8±4.0%, 86.9±2.6%, 83.8±2.9%, 101±6%, 90.3±6.1%, 74.4±8.8%, 104±8%, and 86.5±8.6%, respectively. The developed method was applied to atmospheric particulate matter samples collected in the greater Houston, TX metropolitan area. Ambient concentrations of eight classes of compounds (92 SVOCs) were reported in pg m(-3). PMID:25985427

  19. Chemical characterization of particulate matter suspended in the atmosphere of two Brazilian cities using energy dispersive X-ray fluorescence (EDXRF)

    International Nuclear Information System (INIS)

    The main objective was to evaluate the chemical composition of suspended particulate matter in the atmospheres of Londrina (Parana State) and Piracicaba (Sao Paulo State) - two southern Brazilian cities. The sampling was carried- out in the winter/2002 and summer/2003, with a stacker filter holder, which allowed for the simultaneous collection of fine particles (with aerodynamic diameter smaller than 2.5 μm) and coarse particles (between 2.5 and 10 μm), using 47 mm diameter filters of 0.4 and 8 μm pore diameters, respectively. The sample analyses were carried out with the energy dispersive X-ray fluorescence (EDXRF) technique, using a Mo target X-ray tube and a Si(Li) detector coupled to a multichannel analyzer. The excitation and detection of the characteristic X-rays were done in vacuous (Fe filter, 10 kV, 40 mA) and air atmospheres (Zr filter, 25 kV, 10 mA), quantifying 16 chemical elements in the particulate matter in the range-from Al to Zr. The obtained X-ray spectra were interpreted using the AXIL software and- the chemical element quantification was carried out by the fundamental parameters methodology, employing thin standard films produced by MicroMatter. The accuracy of the analytical method was assessed using a thin glass film, Standard Reference Material produced by the National Bureau of Standards. The average element concentrations in the fine and coarse fractions were different, with S being the major element in the fine fraction in the winter and summer in both cities, and Si, Fe, Al and Ca-in the coarse fraction. The grouping analysis revealed that the elements in the aerosol particles came basically from two sources: soil re-suspension and industrial/anthropogenic activities.

  20. Quality Control Technique for High-Volume Atmospheric Particulate Sampler%大流量大气颗粒物采样器质量控制技术

    Institute of Scientific and Technical Information of China (English)

    常印忠; 王世联; 刘蜀疆; 樊元庆; 赵允刚; 陈占营; 李奇

    2013-01-01

    Quality control technique was developed for high-volume atmospheric particulate sampler. The flow meter of PMS-800 sampler was calibrated by an ISA1932 nozzle flow meter, and the global collection efficiency of PMS-800 sampler was tested by a type 2031 mobile sampler. The results show that the flowrate relative deviation between ISA1932 nozzle flow meter and PMS-800 sampler flow meter is less than 5%, and the global collection efficiency relative deviation between type 2031 sampler and PMS-800 sampler is less than 10%. The performance of PMS-800 sampler meets the specifications with the request of the Comprehensive Nuclear-Test-Ban Treaty. This method can be applied to quality control for high-volume atmospheric particulate sampler.%利用ISA1932喷嘴流量计和2031型采样器,测试了PMS-800大流量大气颗粒物采样器的流量和总采样效率,研究建立了大流量大气颗粒物采样器质量控制方法.结果表明,PMS-800采样器流量计与ISA1932喷嘴流量计的相对偏差小于5%,总采样效率与2031型采样器的相对偏差小于10%,满足全面禁止核试验条约(CTBT)相关技术文件要求.该方法可用于大流量大气颗粒物采样器的质量控制.

  1. Numerical study of atmospheric particulate matters: source apportionment to characterize 3D transport and transformation of precursors and secondary pollutants

    Science.gov (United States)

    Wu, Dongwei

    In recent years, Mainland China, and in particular the industrial hotbed of the Pearl River Delta (PRD) has experienced an increasingly serious problem of high concentrations of airborne particulate matter. Following the tightening-up of China's air quality policies in recent years, and with especially fine particles now added to a new air quality objective, the identification of major source regions and major types of pollutants has become critically important. In this study, a source-oriented method (Particulate Source Apportionment Technology: PSAT) implemented in 3-D Comprehensive Air Quality Model (CAMx), has been applied to analyze how different emission activities impact fine particle concentration in the PRD region. By using this method, a detailed source region and emission category contribution matrix is derived for all regions within the Hong Kong/PRD region. Source appointment results shows that, in summer and spring time, emissions inside PRD region are the major fine particle sources, contribution 70.7% (11.2 mug/m3) and 52.5% (13.1 mug/m3) to the total figure. Super-regional transports are found to be significant in autumn and winter, contribution 58.5% (20.2 mug/m3) and 64.6% (27.8 mug/m3) of the total fine particles in PRD and Hong Kong region. Another important cause of high PM levels has been the transport of fine particles between cities within the PRD region, with three different regions selected for detailed analysis. Results show that mobile vehicle and industry emission are the two major sources for fine particles. Meanwhile, over the same period in Hong Kong, marine proved to be another very significant source of particle pollutant in addition to the significant impact from motor vehicle. Results show that for the Hong Kong/PRD region local reduction of mobile sources and collaboration between different areas could have succeeded in alleviating the air pollution problem.

  2. Application of 2D-GCMS reveals many industrial chemicals in airborne particulate matter

    Science.gov (United States)

    Alam, Mohammed S.; West, Charles E.; Scarlett, Alan G.; Rowland, Steven J.; Harrison, Roy M.

    2013-02-01

    Samples of airborne particulate matter (PM2.5) have been collected in Birmingham, UK and extracted with dichloromethane prior to analysis by two-dimensional GC separation and TOFMS analysis. Identification of compounds using the NIST spectral library has revealed a remarkable diversity of compounds, some of which have not been previously reported in airborne analyses. Groups of compounds identified in this study include a large number of oxygenated VOC including linear and branched compounds, substituted aromatic compounds and alicyclic compounds, oxygenated polycyclic aromatic and alicyclic compounds, organic nitrogen compounds, branched chain VOC and substituted aromatic VOC, phthalates, organo-phosphates and organo-sulphate compounds. Many of the compounds identified are mass production chemicals, which due to their semi-volatility enter the atmosphere and subsequently partition onto pre-existing aerosol. Their contribution to the toxicity of airborne particulate matter is currently unknown but might be significant. The diverse industrial uses and potential sources of the identified compounds are reported.

  3. Gas-particle concentration, distribution, and health risk assessment of polycyclic aromatic hydrocarbons at a traffic area of Giza, Egypt.

    Science.gov (United States)

    Hassan, Salwa Kamal; Khoder, M I

    2012-06-01

    Atmospheric particulate and gaseous polycyclic aromatic hydrocarbons (PAHs) samples were collected from an urban area in Dokki (Giza) during the summer of 2007 and the winter of 2007-2008. The average concentrations of PAHs were 1,429.74 ng/m(3) in the particulate phase, 2,912.56 ng/m(3) in the gaseous phase, and 4,342.30 ng/m(3) in the particulate + gaseous phases during the period of study. Dokki has high level concentrations of PAH compounds compared with many polluted cities in the world. The concentrations of PAH compounds in the particulate and gaseous phases were higher in the winter and lower in the summer. Total concentrations of PAHs in the particulate phase and gaseous phase were 22.58% and 77.42% in summer and 36.97% and 63.03% in winter of the total (particulate + gaseous) concentrations of PAHs, respectively. The gaseous/particulate ratios of PAHs concentration were 3.43 in summer and 1.71 in winter. Significant negative correlation coefficients were found between the ambient temperature and concentrations of the total PAHs in the particulate and gaseous phases. The distribution of individual PAHs and different categories of PAHs based on aromatic ring number in the particulate and gaseous phases during the summer and winter were nearly similar, indicating similar emission sources of PAHs in both two seasons. Benzo(b)fluoranthene in the particulate phase and naphthalene in the gaseous phase were the most abundant compounds. Diagnostic concentration ratios of PAH compounds indicate that these compounds are emitted mainly from pyrogenic sources, mainly local vehicular exhaust emissions. Health risks associated with the inhalation of individual PAHs in particulate and gaseous phases were assessed on the basis of its benzo(a)pyrene equivalent concentration. Dibenzo(a,h)anthracene and benzo(a)pyrene in the particulate phase and benzo(a)pyrene and benzo(a)anthracene in the gaseous phase were the greatest contributors to the total health risks. The

  4. Development of a particulate mass measurement system for tracing pollution sources using atmospheric mercury concentrations and lead isotopes

    Science.gov (United States)

    Pierce, A.; Gustin, M. S.; Christensen, J. N.

    2015-12-01

    The Teledyne Advanced Pollution Instrumentation Model 602 BetaPlus (TAPI) particulate measurement system is a unique platform for non-destructive analysis of PM2.5 mass concentration, and destructive analyses of particulate bound mercury (PBM), perhaps gaseous oxidized mercury (GOM), and lead isotopes. Samples were collected at a flow rate of 16.7 Lpm for 24 hours on 47 mm diameter cation exchange membranes (CEM) for mercury (Hg) and Teflon membranes for lead isotopes. We compared total mercury collected on CEM filters from the TAPI to that collected with the UNR active Hg membrane system and a Tekran 2537/1130/1135 system for gaseous Hg at a highway-impacted site (elev. 1370 m) from December 2013 to November 2015. The TAPI and UNR active system were also compared at a high elevation site (elev. 2515 m) adjacent to the highway-impacted site from December 2013 to October 2014. Data collection using the TAPI and UNR active system started in spring and summer of 2015 at Great Basin National Park (GBNP) in eastern Nevada. The UNR active system consists of three CEM and nylon filters (with backups in series to catch break through) sampling at a rate of 1 Lpm for 1-to-4 weeks. A Tekran total Hg system (Model 2600) was used for analyses of CEM filters from the two membrane systems after digestion. Lead isotope samples from the TAPI were analyzed on a multi-collector ICPMS (IsoProbe). Both the TAPI system and the UNR active system should collect reactive mercury (RM=GOM+PBM) on the CEM filters. TAPI measurements differed from those obtained using the Tekran system depending on season at the low elevation site and were lower than the UNR active system at the highway-impacted site and the high elevation site. We hypothesize that, due to the high flow rate and therefore short retention time, the TAPI captures mainly PBM. Lead isotopes and the chemical forms of GOM measured with the UNR active system can be used to track sources, which is important in rural areas such as GBNP.

  5. Spatial and seasonal variations of atmospheric particulate carbon fractions and identification of secondary sources at urban sites in North India.

    Science.gov (United States)

    Behera, Sailesh N; Sharma, Mukesh

    2015-09-01

    An intensive measurement campaign was undertaken to characterize eight fractions of organic carbon (OC) and elemental carbon (EC) in particulate matter (PM) at four urban sites with different pollution characteristics during summer, post-monsoon, and winter at Kanpur, India. Speciation samplers were used to collect particulate samples on quartz filters followed by analysis of OC and EC using Interagency Monitoring of Protected Visual Environments (IMPROVE)-based thermal/optical reflectance (TOR) method. Based on 24-h average results at each site, the highest levels of OC and EC were observed during winter as 96.7 ± 26.9 and 31.8 ± 9.8 μg/m(3) at residential site and traffic site, respectively. The levels of OC at residential sites during winter appeared to be more than twice of that during summer. The site close to the road traffic had the least value of OC/EC, as 1.77 ± 0.28 during post-monsoon, and the site influenced by emissions of domestic cooking and heating had the highest value of OC/EC, as 4.05 ± 0.79 during winter. The average abundances of OC1, OC2, OC3, OC4, OP, EC1, EC2, and EC3 in total carbon (TC) at all sites for three seasons were 10.03, 19.04, 20.03, 12.32, 10.53, 33.39, 3.21, and 1.99 %, respectively. A sharp increase in levels of OC1 and EC1-OP during winter at two residential sites revealed that biomass burning could be a significant contributor to carbonaceous aerosols. From the application of EC-tracer method, it was observed that contribution of secondary organic carbon (SOC) to PM mass increased from 5 % during post-monsoon to 16 % during winter at residential sites and from 2 % during post-monsoon to 7 % during winter at traffic sites. Therefore, it could be inferred that increase in primary emissions coupled with unfavorable meteorological conditions could cause particle agglomeration and hygroscopic growth, leading to unpleasant pollution episode during winter. PMID:25940490

  6. Atmospheric Dust in the Upper Colorado River Basin: Integrated Analysis of Digital Imagery, Total Suspended Particulate, and Meteorological Data

    Science.gov (United States)

    Urban, F. E.; Reynolds, R. L.; Neff, J. C.; Fernandez, D. P.; Reheis, M. C.; Goldstein, H.; Grote, E.; Landry, C.

    2012-12-01

    Improved measurement and observation of dust emission and deposition in the American west would advance understanding of (1) landscape conditions that promote or suppress dust emission, (2) dynamics of dryland and montane ecosystems, (3) premature melting of snow cover that provides critical water supplies, and (4) possible effects of dust on human health. Such understanding can be applied to issues of land management, water-resource management, as well as the safety and well-being of urban and rural inhabitants. We have recently expanded the scope of particulate measurement in the Upper Colorado River basin through the establishment of total-suspended-particulate (TSP) measurement stations located in Utah and Colorado with bi-weekly data (filter) collection, along with protocols for characterizing dust-on-snow (DOS) layers in Colorado mountains. A sub-network of high-resolution digital cameras has been co-located with several of the TSP stations, as well as at other strategic locations. These real-time regional dust-event detection cameras are internet-based and collect digital imagery every 6-15 minutes. Measurements of meteorological conditions to support these collections and observations are provided partly by CLIM-MET stations, four of which were deployed in 1998 in the Canyonlands (Utah) region. These stations provide continuous, near real-time records of the complex interaction of wind, precipitation, vegetation, as well as dust emission and deposition, in different land-use settings. The complementary datasets of dust measurement and observation enable tracking of individual regional dust events. As an example, the first DOS event of water year 2012 (Nov 5, 2011), as documented at Senator Beck Basin, near Silverton, Colorado, was also recorded by the camera at Island-in-the-Sky (200 km to the northwest), as well as in aeolian activity and wind data from the Dugout Ranch CLIM-MET station (170 km to the west-northwest). At these sites, strong winds and the

  7. Leaf-deposition of particulate matter as a monitoring tool for the urban distribution of atmospheric particles: an experimental and modelling approach

    Science.gov (United States)

    Hofman, Jelle

    Throughout this Ph.D. research, the applicability of biomagnetic monitoring of leaf-deposited particles is evaluated for both monitoring and modelling purposes, using different spatial and temporal scales. First, biomagnetic monitoring of Platanus x acerifofia Willd. leaves was applied to assess the spatial distribution of atmospheric particles throughout an urban street canyon. To investigate the temporal variation of the biomagnetic signal, we evaluated the accumulation behaviour of SIRM by collecting 2-weekly leaf samples of a typical roadside Platanus x acerifolia Willd. tree throughout an entire in-leaf season and examined the seasonal development of the total leaf SIRM signal as well as the leaf-encapsulated fraction. Furthermore, the relevancy of the biomagnetic monitoring approach was evaluated by comparing gravimetric results with SIRM results of leaf-deposited particles within three different size fractions. As biomagnetic monitoring showed to be related to the atmospheric particulate concentration and applicable in urban areas at different Spatial and temporal resolution, the SIRM signal was used for comparison with air quality models at different spatial scales. A micro scale air quality model (ENVI-met RTM) was evaluated, using 96 tree crown sampling locations in a typical urban street canyon, while modelled atmospheric PM10 and NO2 concentrations at the urban scale were compared with leaf SIRM results of ivy (Hedera sp.) at 1 10 locations throughout Antwerp. The last part of this Ph.D. focussed on the influence of tree crown morphology on the distribution and leaf-deposition of atmospheric particles. A model study was conducted to investigate the influence of a detailed LiDAR-derived tree crown, not only on the amount of leaf-deposited particles, but also on the local atmospheric PM distribution in the vicinity of the tree crown. Overall, this Ph.D. demonstrated the application potential of biomagnetic monitoring to gain insights on local ambient PM

  8. Polycyclic peptide therapeutics.

    Science.gov (United States)

    Baeriswyl, Vanessa; Heinis, Christian

    2013-03-01

    Owing to their excellent binding properties, high stability, and low off-target toxicity, polycyclic peptides are an attractive molecule format for the development of therapeutics. Currently, only a handful of polycyclic peptides are used in the clinic; examples include the antibiotic vancomycin, the anticancer drugs actinomycin D and romidepsin, and the analgesic agent ziconotide. All clinically used polycyclic peptide drugs are derived from natural sources, such as soil bacteria in the case of vancomycin, actinomycin D and romidepsin, or the venom of a fish-hunting coil snail in the case of ziconotide. Unfortunately, nature provides peptide macrocyclic ligands for only a small fraction of therapeutic targets. For the generation of ligands of targets of choice, researchers have inserted artificial binding sites into natural polycyclic peptide scaffolds, such as cystine knot proteins, using rational design or directed evolution approaches. More recently, large combinatorial libraries of genetically encoded bicyclic peptides have been generated de novo and screened by phage display. In this Minireview, the properties of existing polycyclic peptide drugs are discussed and related to their interesting molecular architectures. Furthermore, technologies that allow the development of unnatural polycyclic peptide ligands are discussed. Recent application of these technologies has generated promising results, suggesting that polycyclic peptide therapeutics could potentially be developed for a broad range of diseases. PMID:23355488

  9. Annual distribution of allergenic fungal spores in atmospheric particulate matter in the eastern mediterranean; a comparative study between ergosterol and quantitative PCR analysis

    Directory of Open Access Journals (Sweden)

    N. Lang-Yona

    2011-10-01

    Full Text Available Airborne fungal spores are an important fraction of atmospheric particulate matter and are major causative agents of allergenic and infectious diseases. Predicting the variability and species of allergy-causing fungal spores requires detailed and reliable methods for identification and quantification. There are diverse methods for their detection in the atmosphere and in the indoor environments; yet, it is important to optimize suitable methods for characterization of fungal spores in atmospheric samples. In this study we sampled and characterized total and specific airborne fungal spores from PM10 samples collected in Rohovot, Israel over an entire year. The total fungal spore concentrations vary throughout the year although the species variability was nearly the same. Seasonal equivalent spore concentrations analyzed by real-time quantitative-PCR-based methods were fall > winter > spring > summer. Reported concentrations based on ergosterol analysis for the same samples were and fall > spring > winter > summer. Correlation between the two analytical methods was found only for the spring season. These poor associations may be due to the per-spore ergosterol variations that arise from both varying production rates, as well as molecular degradation of ergosterol. While conversion of genome copies to spore concentration is not yet straightforward, the potential for improving this conversion and the ability of qPCR to identify groups of fungi or specific species makes this method preferable for environmental spore quantification. Identifying tools for establishing the relation between the presence of species and the actual ability to induce allergies is still needed in order to predict the effect on human health.

  10. Annual distribution of allergenic fungal spores in atmospheric particulate matter in the Eastern Mediterranean; a comparative study between ergosterol and quantitative PCR analysis

    Directory of Open Access Journals (Sweden)

    N. Lang-Yona

    2012-03-01

    Full Text Available Airborne fungal spores are an important fraction of atmospheric particulate matter and are major causative agents of allergenic and infectious diseases. Predicting the variability and species of allergy-causing fungal spores requires detailed and reliable methods for identification and quantification. There are diverse methods for their detection in the atmosphere and in the indoor environments; yet, it is important to optimize suitable methods for characterization of fungal spores in atmospheric samples. In this study we sampled and characterized total and specific airborne fungal spores from PM10 samples collected in Rehovot, Israel over an entire year. The total fungal spore concentrations vary throughout the year although the species variability was nearly the same. Seasonal equivalent spore concentrations analyzed by real-time quantitative-PCR-based methods were fall > winter > spring > summer. Reported concentrations based on ergosterol analysis for the same samples were and fall > spring > winter > summer. Correlation between the two analytical methods was found only for the spring season. These poor associations may be due to the per-spore ergosterol variations that arise from both varying production rates, as well as molecular degradation of ergosterol. While conversion of genome copies to spore concentration is not yet straightforward, the potential for improving this conversion and the ability of qPCR to identify groups of fungi or specific species makes this method preferable for environmental spore quantification. Identifying tools for establishing the relation between the presence of species and the actual ability to induce allergies is still needed in order to predict the effect on human health.

  11. A Study of the inorganic chemical composition of atmospheric particulate matter in the region of Chekka, North lebanon

    International Nuclear Information System (INIS)

    In North Lebanon, the region of Chekka represents a group of villages scattered around an industrial complex of cement factories and a chemical fertilizer industry. In order to understand the nature of atmospheric aerosols in this region, 20 samples of atmospheric total suspended particles were collected next to the region of industrial activities. The analysis of inorganic water soluble ions and metal composition of the sampled particles was achieved using ion chromatography (I.C.) and inductively coupled plasma-mass spectrometer (ICP-MS). Higher global particle concentrations and NO-3 concentrations were identified in the sites near the cement factories. However, this nitrate concentration was attributed to long range transport and accumulation phenomenon happening in the region. Peaks in potassium concentrations were confirmed in some samples and most probably emitted by a secondary source of emissions, possibly from local biomass combustion. On the other hand, low levels of calcium were identified in the samples, despite the presence of cement quarries next to the sampling sites, because of the dominant low wind activity during the sampling period. (author).

  12. Trueness, Precision, and Detectability for Sampling and Analysis of Organic Species in Airborne Particulate Matter

    Science.gov (United States)

    Recovery. precision, limits of detection and quantitation, blank levels, calibration linearity, and agreement with certified reference materials were determined for two classes of organic components of airborne particulate matter, polycyclic aromatic hydrocarbons and hopanes usin...

  13. Correlation analysis of the urban heat island effect and the spatial and temporal distribution of atmospheric particulates using TM images in Beijing

    International Nuclear Information System (INIS)

    This study combines the methods of observation statistics and remote sensing retrieval, using remote sensing information including the urban heat island (UHI) intensity index, the normalized difference vegetation index (NDVI), the normalized difference water index (NDWI), and the difference vegetation index (DVI) to analyze the correlation between the urban heat island effect and the spatial and temporal concentration distributions of atmospheric particulates in Beijing. The analysis establishes (1) a direct correlation between UHI and DVI; (2) an indirect correlation among UHI, NDWI and DVI; and (3) an indirect correlation among UHI, NDVI, and DVI. The results proved the existence of three correlation types with regional and seasonal effects and revealed an interesting correlation between UHI and DVI, that is, if UHI is below 0.1, then DVI increases with the increase in UHI, and vice versa. Also, DVI changes more with UHI in the two middle zones of Beijing. -- Highlights: •We analyze the correlation from the spatial and temporal views. •We present correlation analyses among UHI, NDWI, NDVI, and DVI from three perspectives. •Three correlations are proven to exist with regional and seasonal effects. •If UHI is below 0.1, then DVI increases with the increase in UHI, and vice versa. •The DVI changes more with UHI in the two middle zones of Beijing. -- Generally, if UHI is below 0.1 in the weak heat island or green island range, then DVI increases with the increase in UHI, and vice versa

  14. DNA-damage effect of polycyclic aromatic hydrocarbons from urban area, evaluated in lung fibroblast cultures

    International Nuclear Information System (INIS)

    This study was designed to biomonitor the effect of PAH extracts from urban areas on the DNA of lung cell cultures. The analyses of the polycyclic aromatic hydrocarbons (PAHs) were performed in atmospheric PM2.5 and PM10 collected at three sampling sites with heavy traffic located in the Metropolitan Area of Porto Alegre (MAPA) (Brazil). The concentrations of 16 major PAHs were determined according to EPA. Comet assay on V79 hamster lung cells was chosen for genotoxicity evaluation. Temperature, humidity, and wind speed were recorded. With regard to the damage index, higher levels were reported in the extract of particulate matter samples from the MAPA during the summer. High molecular weight compounds showed correlation with DNA damage frequency and their respective carcinogenicity. - Highlights: ► Cell line V79 was used to assess the effect of PAHs in PM2.5 and PM10 from urban area. ► Temperature showed a significant seasonal variation with the level of DNA damage. ► PAHs with higher molecular weight contributed to higher DNA damage levels. - DNA-damage effect of polycyclic aromatic hydrocarbons from urban area, showed difference according to season

  15. Chemistry of atmospheric precipitation in the north-central united states: Influence of sulfate, nitrate, ammonia and calcareous soil particulates

    Science.gov (United States)

    Munger, James William

    The supply of alkaline soil dust and gaseous NH 3 available to neutralize anthropogenic acids in the atmosphere controls the acidity of precipitation in the north-central United States. Major ions and trace metals were determined in precipitation-event and snow-core samples from sites along a 600 km transect from the North Dakota prairie to the forests of northeastern Minnesota, collected during the period April 1978-June 1979. Acidity increased 4-fold from west to east as the effect of alkaline dust and NH 3 decreased with increasing distance from the cultivated prairie; calcium and Mg 2+ decreased 2 to 3-fold across the transect. However, minimum concentrations of NH 4+ and SO 42- were observed at Itasca, the central site. Natural emissions of these elements were important in the west, while anthropogenic emissions were responsible for the higher concentrations in the east. Wet deposition of H + decreased 8-fold and deposition of NO 3- and SO 42- decreased 1.5 to 2-fold from Hovland in the east to Tewaukon in the west. Wet deposition of the metal cations increased from Hovland to Tewaukon. Dry deposition followed a similar trend. Winter snow cover and freezing temperatures, which decreased airborne soil dust and the evolution of NH 3 from the prairie soils, led to an increase in precipitation acidity at all sites. The acid increase was accompanied by a decrease in alkaline metal cations, especially Ca 2+, and in NH 4+. At Hovland SO 42- and NO 3- also increased during the winter. The occurrence of snow events at Tewaukon that were appreciably more acid than the snowpack accumulated there indicates that snow was neutralized after it fell by alkaline dust entrained in resuspended snow, or deposited separately. Winter inputs of acid are especially important because they are released during a short period in the spring. Over half of the acid input at Hovland occurred during the winter. Precipitation inputs of P and N probably benefit nutrient-poor ecosystems in the

  16. Distribution Characteristics of Particulate Mercury in Atmosphere of Nanjing during Winter%南京市冬季大气颗粒态汞的分布特征

    Institute of Scientific and Technical Information of China (English)

    于学珍; 谢云中; 李贺

    2013-01-01

    采集了南京市2012年冬季4个功能区的PM2.5、PM10、TSP样品,对不同粒径大气颗粒物中的颗粒态汞测试。结果表明,南京冬季大气颗粒物TSP中汞的质量浓度为49.26 pg/m3~257.14 pg/m3,平均质量浓度为161.27 pg/m3;PM10中汞的质量浓度为44.82 pg/m3~228.29 pg/m3,平均质量浓度为147.38 pg/m3;PM2.5中汞的质量浓度为35.98 pg/m3~178.58 pg/m3,平均质量浓度为104.10 pg/m3。不同功能区大气颗粒态汞质量浓度的分布趋势为:交通综合区>旅游区>住宿综合区>商业区。大气颗粒态汞60%以上存在于可吸入肺的PM2.5中,细颗粒物富集汞的能力比粗颗粒物强。%The samples of the PM2.5, PM10, TSP were collected in four functional sites of Nanjing during winter in 2012 , and the particular mercury concentrations in different size were analyzed .The results indicated that the mercury concentrations of TSP were 49.26 pg/m3 ~257.14 pg/m3 , the average concentration was 161.27 pg/m3.The mercury concentrations of PM10 were 44.82 pg/m3 ~228.29 pg/m3, the average concen-tration was 147.38 pg/m3.The mercury concentrations of PM2.5 were 35.98 pg/m3 ~178.58 pg/m3, the aver-age concentration was 104 .10 pg/m3 .The sequence of atmospheric particulate mercury concentration in different functional areas was:traffic district >tourist area >residential district >business district .More than 60%of particulates mercury was combined with fine aerosol , which can be inhaled into the lungs .The fine particulate matters enrich mercury much easier than the coarse particles .

  17. 灰霾期间大气颗粒物污染特征研究进展%Research Progresses on Pollution Characteristics of Atmospheric Particulate Matter during Haze Period

    Institute of Scientific and Technical Information of China (English)

    王剑; 徐美; 叶霞; 张翠华; 张文育

    2015-01-01

    In recent years, with the rapid development of economy and the speeding up of urbanization, the haze weather shows increasing trend and causes the attention of the society. The contamination level, size distribution and vertical distribution of atmospheric particulate matter during the haze period were introduced, the concentration level and the size distribution of water-soluble ions, organic and elemental carbon and metal elements in the atmospheric particulate matter were described, and the source analysis methods of atmospheric particulate matter were summarized. Some advices on the prevention and control measures of the haze weather were proposed.%近年来,随着经济的迅速发展和城市化进程的加快,灰霾天气呈现增加的趋势,引起了社会的高度关注。综述了灰霾发生时大气颗粒物污染水平、粒径分布和垂直分布特征,大气颗粒物重要化学成分(水溶性离子、有机碳和元素碳、金属元素)的浓度水平和粒径分布特征及大气颗粒物的来源解析方法,并提出灰霾主要防治措施。

  18. A theoretical investigation of radiative effects and microphysical processes involved in the interaction of aerosol particulates in the atmosphere and validation of the theoretical results with the INDOEX observations

    International Nuclear Information System (INIS)

    A theoretical approach, which is based on certain physical assumptions and quantum physical concepts, has been extended to investigate the radiative effects and the microphysical properties involved in the interaction of aerosol particulates in the atmosphere which may have important climatic effect. The theoretical findings are used to validate some of the observations of Indian Ocean Experiment (INDOEX) during its First Field Phase-98 (FFP-98) and Intense Field Phase-99 (IFP-99). The aerosol optical depth and the radiative forcing of the surface and the top of the atmosphere are computed and the results are found to have a good correspondence with the INDOEX results

  19. Influence of in-port ships emissions to gaseous atmospheric pollutants and to particulate matter of different sizes in a Mediterranean harbour in Italy

    Science.gov (United States)

    Merico, E.; Donateo, A.; Gambaro, A.; Cesari, D.; Gregoris, E.; Barbaro, E.; Dinoi, A.; Giovanelli, G.; Masieri, S.; Contini, D.

    2016-08-01

    Ship emissions are a growing concern, especially in coastal areas, for potential impacts on human health and climate. International mitigation strategies to curb these emission, based on low-sulphur content fuels, have proven useful to improve local air quality. However, the effect on climate forcing is less obvious. Detailed information on the influence of shipping to particles of different sizes is needed to investigate air quality and climate interaction. In this work, the contributions of maritime emissions to atmospheric concentrations of gaseous pollutants (NO, NO2, SO2, and O3) and of particles (sizes from 0.009 μm to 30 μm) were investigated considering manoeuvring (arrival and departure of ships) and hotelling phases (including loading/unloading activities). Results showed that the size distributions of shipping contributions were different for the two phases and could be efficiently described, using measured data, considering four size-ranges. The largest contribution to particles concentration was observed for Dp < 0.25 μm, however, a secondary maximum was observed at Dp = 0.35 μm. The minimum contribution was observed at Dp around 0.8-0.9 μm with a negligible contribution from hotelling for size range 0.4-1 μm. The comparison of 2012 and 2014 datasets showed no significant changes of gaseous and particulate pollutant emissions and of the contribution to particle mass concentration. However, an increase of the contribution to particle number concentration (PNC) was observed. Results suggested that harbour logistic has a relevant role in determining the total impact of shipping on air quality of the nearby coastal areas. Additionally, future policies should focus on PNC that represents an important fraction of emissions also for low-sulphur fuels. DOAS remote sensing proved a useful tool to directly measure NO2 and SO2 ship emissions giving estimates comparable with those of emission inventory approach.

  20. Bulky PAH-DNA induced by exposure of a co-culture model of human alveolar macrophages and embryonic epithelial cells to atmospheric particulate pollution; Adduits encombrants a l'ADN dans des cocultures de cellules pulmonaires humaines exposees a une pollution atmospherique particulaire

    Energy Technology Data Exchange (ETDEWEB)

    Abbas, Imane; Garcon, Guillaume; Billet, Sylvain; Shirali, Pirouz [Universite Lille Nord de France - Lille (France); Unite de Chimie Environnementale et Interactions sur le Vivant, MREI, Universite du Littoral Cote d' Opale, Dunkerque (France); Andre, Veronique; Le Goff, Jeremie; Sichel, Francois [GRECAN, Universite de Caen Basse-Normandie et centre Francois Baclesse, Caen (France); Roy Saint-Georges, Francoise; Mulliez, Philippe [Service de Pneumologie, Hopital Saint-Philibert, GHICL, Lille (France)

    2012-01-15

    Because of their deep penetration in human lungs, fine airborne particulate matter were described as mainly responsible for the deleterious effects of exposure to air pollution on health. Organic constituents are adsorbed on particles surface and, after inhalation, some (polycyclic aromatic hydrocarbons, PAHs) can be activated into reactive metabolites and can bind to DNA. The formation of bulky DNA adducts has been researched after exposure of mono-and co-cultures of alveolar macrophages (AM) and human embryonic human lung epithelial (L132), to fine air pollution particulate matter Air samples have been collected with cascade impactor and characterized: size distribution (92.15% < 2.5{mu}.m), specific surface area (1 m{sup 2}/g), inorganic (Fe, AI, Ca, Na, K, Mg, Pb, etc.) and organic compounds (PAHs, etc.). {sup 32}P post-labeling method was applied to detect bulky DNA adducts in AM and L132, in mono-and co-cultures, 72 h after their exposure to atmospheric particles at their Lethals and Effects concentrations or (LC or CE) to 50% (i.e. MA: EC{sub 50} = 74.63 {mu}g/mL and L132: LC-5-0 = 75.36 {mu}g/mL). Exposure to desorbed particles (MA: C1= 61.11 {mu}g/mL and L132 : C2 = 61.71 {mu}g/mL) and B[a]P (1 {mu}M) were included. Bulky PAH-DNA adducts were detected in AM in mono-culture after exposure to total particles (Pt), to B[a]P and desorbed particles (Pd). Whatever the exposure, no DNA adduct was detected in L132 in mono-culture. These results are coherent with the enzymatic activities of cytochrome P450 l Al in AM and L132. Exposure of co-culture to Pt, or Pd induced bulky adducts to DNA in AM but not in L132. Exposure to B[a]P alone has altered the DNA of AM and L132, in co-culture. Exposure to Pt is closer to the environmental conditions, but conferred an exposure to amounts of genotoxic agents compared to studies using organic extracts. The formation of bulky DNA adducts was nevertheless observed in AM exposed to Pt, in mono- or co-culture, indicating that

  1. Spatial and Seasonal Variations of Polycyclic Aromatic Hydrocarbons (PAHs) in Ambient Particulate Matter (PM10, PM2.5) in Three Mega-Cities in China and Identification of Major Contributing Source Types.

    Science.gov (United States)

    Zhang, Linlin; Chen, Rui; Lv, Jungang

    2016-06-01

    Beijing, is the political, economic and cultural center of China. Tianjin and Shijiazhuang, located close to Beijing are also two mega-cities with huge population. The rapid economic development in the three cities in the last decades has caused severe air pollution problems, especially airborne PAHs pollution, in both gaseous and particulate phases, which has resulted in considerable harm to the health of local residents. In this study, a total of 671 air samples were collected in the three cities and reference site, and four national air quality background sites. Concentrations and seasonal variations were discussed to describe the pollution status and identify possible sources. The results showed that concentrations of BaP, a PAH that serves as an indicator of PAH pollution, exceeded the Chinese national standard by 4-12 times. PAH concentrations varied significantly in different seasons, with similar trends in the three cities. The toxic equivalents quantity (i.e., quantity of total PAHs with an equivalent toxicity to BaP) ranged from 13.35 to 22.54 ng/m(3) during the central heating period of winter and spring. These concentrations greatly exceeded the Chinese national standards for 24-h average (2.5 ng/m(3)) and annual average (1.0 ng/m(3)) concentrations of BaP. Two ratios that are indicative of PAH source, Pyr/BaP and BaP/BghiP, revealed that high percentages of the PAH pollution were contributed by coal combustion. PMID:27107589

  2. Assessing effects of seasonal variation on occupational exposure of newsagent kiosks to polycyclic aromatic hydrocarbons found in the urban atmosphere of Tehran Metropolitan

    Directory of Open Access Journals (Sweden)

    F Rezaei

    2015-08-01

    Full Text Available Background and Objectives: PAHs are main components of urban air pollution and are mutagenic for human being. Seasonal variations have effects on the amount of exposure to PAHs. The objectives of this research were to determine the amount of newsagent’s exposure to PAHs found in the urban atmosphere of Tehran City during warm and cold periods and comparing exposure levels in two periods. Materials and Methods: The assessment of personal exposure was performed based on NIOSH method 5515 and was analyzed by gas chromatography–mass spectrometry (GC/MS. Mann- Whitney test was used to determine the effects of seasonal variation on the amount of newsagent’s exposure to PAHs. Results: The mean levels of newsagent’s exposure to benzo[a]pyrene in the south area of Tehran City were 0.148±0.010 and 0.417±0.041 μg/m3 in summer and autumn seasons respectively. The amount was higher than the mean levels of newsagent’s exposure in other geographic areas of city. The levels of newsagent’s exposure to all PAHs (p<0.001 were significantly higher in autumn compared with summer. Conclusion: The levels of exposure to PAHs during autumn were 2 to 3 fold higher than the levels of exposure during summer. Newsagents in the south area of Tehran City were experiencing higher levels of exposures to PAHs.

  3. 长清地区春季大气中颗粒物的SEM观察与分析%SEM Observation and Analysis of Atmospheric Particulate Matters in Spring Season at Changqing Region

    Institute of Scientific and Technical Information of China (English)

    杨永成; 张晓凯; 李超群; 李学; 康丽莎

    2015-01-01

    利用扫描电镜观察分析了长清地区春季大气中颗粒物显微形态及粒径分布状况,采用统计回归分析方法绘制了连续30 d的大气颗粒物粒径与数量分布状况关系曲线及相应的柱状图.试验结果表明:大气颗粒物主要集中在0~1.0μm和1.0~2.5μm的粒径范围内,显微形态有不规则的颗粒状、块状、圆球状、棒状和片状等.另外,还观察到了杆菌和花粉的显微形态.试验结果对于研究大气中PM2.5、PM10及大气污染状况具有一定的参考价值.%The microstructure and particle size and distribution of the atmospheric particulate matters were observed in the spring time in Changqing area by use of a scanning electron microscope. The relation curve and histogram of the particle size and distribution of the quantity of atmospheric particulates during a continuous thirty days was drawn using the statistical regression analysis method. The experimental results showed that atmospheric particulates were mainly in a particle size range of 0 ~1. 0 μm and 1. 0 ~2. 5 μm. The microstructure of atmospheric particulate matters included irregular particle, block, spherosome, clava, chip, etc. In addition, the microstructures of Escherichia coli and pollen are observed. The experimental results have reference value to the research of PM2. 5 and PM10 in atmosphere and the atmospheric contamination to some extent. And the experimental method is worthy to be applied widely.

  4. [How do transport and metabolism affect the biological effects of polycyclic aromatic hydrocarbons?].

    Science.gov (United States)

    Bekki, Kanae; Toriba, Akira; Tang, Ning; Kameda, Takayuki; Takigami, Hidetaka; Suzuki, Go; Hayakawa, Kazuichi

    2012-01-01

    Polycyclic aromatic hydrocarbons (PAHs), some of which are carcinogenic/mutagenic, are generated by combustion of fossil fuels and also released through tanker or oilfield accident to cause a large scale environmental pollution. PAHs concentration in China is especially high in East Asia because of many kinds of generation sources such as coal heating systems, vehicles and factories without exhaust gas/particulate treatment systems. So, the atmospheric pollution caused by PAHs in China has been seriously concerned from the view point of health effects. Like yellow sand and sulfur oxide, PAHs exhausted in China are also transported to Japan. Additionally, strongly mutagenic nitrated PAHs (NPAHs), estrogenic/antiestrogenic PAH hydroxides (PAHOHs) and reactive oxygen species-producing PAH quinones (PAHQs) are formed from PAHs by the chemical reaction during the transport. Furthermore these PAHOHs and PAHQs are produced by the metabolism in animal body. In the biological activities caused by the above PAH derivatives, the structure-activity relationship was observed. In this review, our recent results on the generation of PAH derivatives by atmospheric transport and metabolism are reported. Also, the existing condition of PAHs as atmospheric pollutants is considered. PMID:22382837

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

    Science.gov (United States)

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

    2014-12-01

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

  6. Investigation of time-resolved atmospheric conditions and indoor/outdoor particulate matter concentrations in homes with gas and biomass cook stoves in Nogales, Sonora, Mexico.

    Science.gov (United States)

    Holmes, Heather A; Pardyjak, Eric R

    2014-07-01

    This paper reports findings from a case study designed to investigate indoor and outdoor air quality in homes near the United States-Mexico border During the field study, size-resolved continuous particulate matter (PM) concentrations were measured in six homes, while outdoor PM was simultaneously monitored at the same location in Nogales, Sonora, Mexico, during March 14-30, 2009. The purpose of the experiment was to compare PM in homes using different fuels for cooking, gas versus biomass, and to obtain a spatial distribution of outdoor PM in a region where local sources vary significantly (e.g., highway, border crossing, unpaved roads, industry). Continuous PM data were collected every 6 seconds using a valve switching system to sample indoor and outdoor air at each home location. This paper presents the indoor PM data from each home, including the relationship between indoor and outdoor PM. The meteorological conditions associated with elevated ambient PM events in the region are also discussed. Results indicate that indoor air pollution has a strong dependence on cooking fuel, with gas stoves having hourly averaged median PM3 concentrations in the range of 134 to 157 microg m(-3) and biomass stoves 163 to 504 microg m(-1). Outdoor PM also indicates a large spatial heterogeneity due to the presence of microscale sources and meteorological influences (median PM3: 130 to 770 microg m(-3)). The former is evident in the median and range of daytime PM values (median PM3: 250 microg m(-3), maximum: 9411 microg m(-3)), while the meteorological influences appear to be dominant during nighttime periods (median PM3: 251 microg m(-3), maximum: 10,846 microg m(-3)). The atmospheric stability is quantified for three nighttime temperature inversion episodes, which were associated with an order of magnitude increase in PM10 at the regulatory monitor in Nogales, AZ (maximum increase: 12 to 474 microg m(-3)). Implications: Regulatory air quality standards are based on outdoor

  7. Risk of PAHs on salmon (Assessing mechanisms of immunotoxicity for polycyclic aromatic hydrocarbons)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Juvenile rainbow trout were fed a diet containing an environmentally relevant mixture of 10 high molecular weight polycyclic aromatic hydrocarbons (PAHs) at a dose...

  8. Investigation of the ionization mechanism of polycyclic aromatic hydrocarbons using an ethanol/bromobenzene/chlorobenzene/anisole mixture as a dopant in liquid chromatography/atmospheric pressure photoionization mass spectrometry

    KAUST Repository

    Amad, Maan H.

    2012-09-23

    RATIONALE An ethanol-based multicomponent dopant consisting of ethanol/chlorobenzene/bromobenzene/anisole (98.975:0.1:0.9:0.025, v/v/v/v) has been used as a dopant for atmospheric pressure photoionization (APPI) of polycyclic aromatic hydrocarbons (PAHs). In this study the mechanism of ionization of PAHs assisted by the ethanol-based multicomponent dopant is investigated. METHODS The reactant background cluster ions of the ethanol-based multicomponent dopant observed in the positive ion APPI were studied. These studies were performed to investigate the mechanism behind the generation of a molecular radical cation (M +•) for PAHs by APPI assisted by the ethanol-based multicomponent dopant. Full scan and MS/MS analyses were conducted using an LTQ Orbitrap mass spectrometer. The effect of acidification of the mobile phase on the dopant cluster ion formation was also investigated. RESULTS With the ethanol-based multicomponent dopant, a single type of molecular radical cation M +• was observed for the studied PAHs. The characteristic ion signal of the multicomponent dopant mixture consisted of mainly anisole photoions at m/z 108.05697 and its adduct ions at m/z 124.05188 and 164.07061. The anisole ion response at m/z 108.05697 was stable in the presence of acetonitrile, methanol, water and 0.1% formic acid mobile phase composition. CONCLUSIONS The abundance formation of anisole photoions shows the universality of this multicomponent dopant in ionizing compounds with ionization energy ranging from 7.1-8.2 eV. Since the ionization energy of anisole is 8.2 eV and is lower than those of chlorobenzene (9.07 eV) and bromobenzene (9.0 eV), the mechanism of formation of anisole photoions even with its very minute amounts was not only governed by its photoionization by the krypton lamp photon energy (10.0 eV and 10.6 eV), but also by charge transfer from bromobenzene and chlorobenzene radical cations. PAH molecules were mainly ionized by charge transfer reaction from

  9. Sulfur dioxide and particulates as atmospheric pollution vectors. El dioxide de Azufre la materia particulada como vectores de la contaminacion atmosferica

    Energy Technology Data Exchange (ETDEWEB)

    Cabeza, J.M.

    1993-01-01

    Samples taken from 1 st January 1990 till 31st December 1991 at different locations in Spain are presented. From these results and using priority lists and indexes suggested in the literature, the main conclusion is that sulfur dioxide and particulates are not a danger for the public health in the city of Aviles (one of the most contaminated cities in Spain). (Author)

  10. Particulate matter dynamics

    CERN Document Server

    Cionco, Rodolfo G; Caligaris, Marta G

    2012-01-01

    A substantial fraction of the particulate matter released into the atmosphere by industrial or natural processes corresponds to particles whose aerodynamic diameters are greater than 50 mm. It has been shown that, for these particles, the classical description of Gaussian plume diffusion processes, is inadequate to describe the transport and deposition. In this paper we present new results concerning the dispersion of coarse particulate matter. The simulations are done with our own code that uses the Bulirsch Stoer numerical integrator to calculate threedimensional trajectories of particles released into the environment under very general conditions. Turbulent processes are simulated by the Langevin equation and weather conditions are modeled after stable (Monin-Obukhov length L> 0) and unstable conditions (L <0). We present several case studies based on Monte Carlo simulations and discusses the effect of weather on the final deposition of these particles.

  11. Nitrated polycyclic aromatic hydrocarbon pollution during the Shanghai World Expo 2010

    Science.gov (United States)

    Wang, W.; Jing, L.; Zhan, J.; Wang, B.; Zhang, D. P.; Zhang, H. W.; Wang, D. Q.; Yang, Y.; Zhao, J.; Sun, Y. F.; Bi, X. H.; Wang, X. T.; Feng, J. L.

    2014-06-01

    Atmospheric particulate matter with aerodynamic diameter China in 2010 when the World Expo took place. Eight nitrated polycyclic aromatic hydrocarbons (NPAHs) were analyzed. Significant reductions in individual NPAH (69-324%) and the mean ΣNPAH (about 140%) concentrations were measured during the Expo period. In order to minimize the influence from the meteorological condition, individual NPAH concentrations of 2010 Expo period were compared with those in the same time period from 2008. Significant effects from the source control measures were revealed, i.e., the individual NPAH concentration reductions ranged between 31% and 477% at the mixed residential and industrial Baoshan site, and only 0-88% at the urban Xujiahui site. The relatively high 2-nitrofluoranthene/1-nitropyrene ratio values (11-31) suggested a predominance of photochemical formation of NPAHs in the atmosphere during the Expo period. It could be concluded that the air quality during the Shanghai World Expo 2010 was benefited from the following three factors; (1) source control measures during the Expo period, i.e., prohibition of open field biomass burning in surrounding areas, (2) the three-year plan implemented from October 1, 2009, including construction sites shut-down, flue-gas desulfurization/denitrification and the vehicle upgradation and (3) the Asian monsoon which brings in clean air from the ocean during spring and summer into Shanghai.

  12. Aperiodic Subshifts on Polycyclic Groups

    OpenAIRE

    Jeandel, Emmanuel

    2016-01-01

    Previous version had a mistake in the proof of the polycyclic case. The new proof needs a very strong new result by Barbieri and Sablik, that the authors hopes is avoidable We prove that every polycyclic group of nonlinear growth admits a strongly aperiodic SFT and has an undecidable domino problem. This answers a question of [4] and generalizes the result of [2].

  13. Phototransformation of Polycyclic Aromatic Hydrocarbons (PAHs) on a Non-Semi Conductive Surface Such as Silica

    Energy Technology Data Exchange (ETDEWEB)

    Dabestani, R., Sigman, M.E.

    1997-09-16

    Polycyclic aromatic hydrocarbons (PAH), by products of fossil fuel production and consumption, constitute a large class of environmental pollutants. These toxic and sometimes carcinogenic compounds are also found in coal tar and fly ash. When released into the air, they can be sorbed onto particulates present in the atmosphere where they find their way into soil and ground water upon being washed by rain. During their residence time in the environment, PAHs will be exposed to solar radiation and may undergo phototransformation to other products. Thus, light induced photodegradation of PM`s at the solid/air interfaces can play a significant role in their depletion. Light-induced processes have been claimed to enhance transformation of these PM`s in the environment. However, detailed studies on the nature and identities of photoproducts formed during the transformation of these compounds on solid surfaces is scarce. Since insulators such as silica, alumina,silicoaluminates and calcium carbonate are believed to constitute up 20-30% of inorganic particulates present in the atmosphere, they serve as environmentally relevant model surfaces to study the photophysical and photochemical behavior of PM`s. Although photochemistry of organic compounds adsorbed on solid surfaces has received much attention in recent years, the specific properties of the interface which influence photoprocesses and the exact mechanism of interaction between a surface and a substrate are often not well understood. We have investigated the photochemistry of many PAHs including eight that are on Environmental Protection Agency`s (EPA) sixteen priority pollutant PAH list shown in Table 1 at silica/air interface.

  14. Characterization and source identification of fine particulate matter in the atmosphere of downtown Shanghai using μ-SXRF and ICP-MS

    International Nuclear Information System (INIS)

    To investigate the characteristic and sources of the fine particulate matter (PM2.5), and the major sources affecting particulate air pollution in Shanghai, China, the individual aerosol particles were analyzed using the synchrotron radiation micro-beam X-ray fluorescence analysis (μ-SXRF), and the PM2.5 multi-elements were determined by the inductively coupled plasma mass spectrometer (ICP-MS). The results show that the mass concentration and chemical elements have seasonal variation, and the enrichment factors show that the chemical elements in the inhalable particles could come from the earth crust and anthropogenic pollution. The extent of metal pollution was assessed by comparing the measured concentrations with those reported in the literature. Nine categories of PM2.5 pollution sources identified at the center of Shanghai show that the vehicle exhaust, emission of metallurgic industry and coal combustion are important. (authors)

  15. 40 CFR 60.142 - Standard for particulate matter.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for particulate matter. 60.142....142 Standard for particulate matter. (a) Except as provided under paragraph (b) of this section, on... the atmosphere from any affected facility any gases which: (1) Contain particulate matter in excess...

  16. 40 CFR 60.52 - Standard for particulate matter.

    Science.gov (United States)

    2010-07-01

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

  17. Polycyclic aromatic hydrocarbons in soils of Beijing and Tianjin region: vertical distribution, correlation with TOC and transport mechanism

    Institute of Scientific and Technical Information of China (English)

    HE Fengpeng; ZHANG Zhihuan; WAN Yunyang; LU Song; WANG Liang; BU Qingwei

    2009-01-01

    Concentrations and compositions of 20 polycyclic aromatic hydrocarbons (PAHs) or heterocyclic aromatic hydrocarbons (HAHs) were investigated in 16 soil profiles of Beijing and Tianjin region. Transport of high molecular weight PAHs (HMWPAHs) and correlation between total organic carbon (TOC) and the concentrations were also discussed. The results indicated that highly contaminated sites were located at urban or wastewater irrigation areas and pollutants mainly accumulated in topsoil (<40 cm), with a sharp content decrease at the vertical boundary of 30--40 cm. Total PAHs/HAHs concentrations in soils from Tianjin were markedly greater than those from Beijing. Even the contents at bottoms of soil profiles in Tianjin were higher than those in topsoils of Beijing soil profile. HMWPAHs (4-6 rings PAHs) dominated the PAH profiles, exhibiting a uniform distribution of pyrogenic origin between topsoils and deep layers. Furthermore, the percentages of HMWPAHs remained relative constant with the depth of soil profiles, which were consistent with the distribution of particulate matter-associated PAHs in the local atmospheric environments. Therefore, HMWPAHs transport with particulates might be the predominant source found in soil profiles.

  18. Metabolism of polycyclic aromatic hydrocarbons in benthic microcosms

    International Nuclear Information System (INIS)

    [12-14C]Benz(a)anthracene was used as a tracer to follow the metabolism of polycyclic aromatic hydrocarbons in benthic microcosms containing fine sediment and polychaetes. Experiments were conducted using both large (230 L) and small (2 L) microcosms where the fate of the radiolabel was followed for up to 42 days in the water column, in the sediment reservoir, and in two species of polychaetes (Nereis virens and Nephtys incisa). Benz(a)anthracene was extensively metabolized in these microcosms, although the degree of metabolism was highly dependent on how the radiolabel was introduced to the system and the presence of suspended particulates and an established microbial community

  19. Exposure of iron foundry workers to polycyclic aromatic hydrocarbons

    DEFF Research Database (Denmark)

    Omland, Øyvind; Sherson, D; Hansen, Åse Marie;

    1994-01-01

    (ELISA) and reverse phase high performance liquid chromatography (HPLC), respectively. 70 male foundry workers and 68 matched controls were investigated. High and low exposure groups were defined from breathing zone hygienic samples, consisting of 16 PAH compounds in particulate and gaseous phase. Mean...... than in smoking and non-smoking controls (0 (0-0.022) and 0 (0-0.010) mumol/mol creatinine). Dose-response relations between total PAH, pyrene, carcinogenic PAHs, and 1-hydroxypyrene for smokers, and polycyclic aromatic hydrocarbons adsorbed to dust for non-smokers are suggested. Exposure to PAHs...

  20. Bioassay of polycyclic aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Van Kirk, E.A.

    1980-08-01

    A positive relationship was found between the photodynamic activity of 24 polycyclic aromatic hydrocarbons versus published results on the mutagenicity, carcinogenicity, and initiation of unscheduled DNA synthesis. Metabolic activation of benzo(a)pyrene resulted in detection of increased mutagenesis in Paramecium tetraurelia as found also in the Ames Salmonella assay. The utility of P. tetraurelia as a biological detector of hazardous polycyclic aromatic hydrocarbons is discussed.

  1. Aliphatic and polycyclic aromatic hydrocarbons characterisation of Coimbra and Oporto PM2.5 urban aerosol

    Science.gov (United States)

    Rocha, A. C.; Mirante, F.; Gonçalves, C.; Nunes, T.; Alves, C.; Evtyugina, M.; Kowacz, M.; Pio, C.; Rocha, C.; Vasconcelos, T.

    2009-04-01

    The concentration of organic pollutants in urban areas is mostly due to incomplete combustion from vehicles, industries and domestic heating. Some of these compounds, principally the aliphatic (ALIPH) and polycyclic aromatic hydrocarbons (PAHs) promote harmful effects in human health. The determination of the ALIPH and PAHs concentration levels and their possible emission sources are useful for air quality management and source apportionment studies. In order to estimate and compare the ambient concentrations and establish the main sources of these compounds, the fine fraction of the atmospheric particulate matter (PM2.5) was collected simultaneously in Oporto and Coimbra during summer and winter seasons using a high volume sampler. The organic compounds were extracted from the particulate matter, under reflux with dichloromethane and the total organic extract (TOE) was fractionated by flash chromatography using five different eluents with increasing polarity. The hydrocarbon fractions were analysed by gas chromatography/mass spectrometry (GC/MS). Here we present and discuss the qualitative and quantitative composition of the aliphatic and aromatic fractions present in PM2.5 samples from both cities. The homologous series of C14 to C34 n-alkanes, isoprenoid hydrocarbons (pristane and phytane), PAHs and some petroleum markers have been identified and quantified. With the purpose of identifying the possible sources, various molecular diagnostic ratios were calculated. The global carbon preference index (CPI) closer to the unity, the large concentration of the unresolved complex mixture (UCM) and the presence of PAHs indicate that motor vehicle exhaust was the main emission source of the aliphatic and polycyclic aromatic fractions of Oporto and Coimbra aerosol, especially in the first city. Also, the remarkable presence of petroleum biomarkers such, as hopanes, confirms the previous results. Concentration ratios between PAHs were calculated and used to assign emission

  2. Retrieval of the optical depth and vertical distribution of particulate scatterers in the atmosphere using O2 A- and B-band SCIAMACHY observations over Kanpur: a case study

    Directory of Open Access Journals (Sweden)

    U. Platt

    2012-05-01

    Full Text Available Due to the well-defined vertical profile of O2 in the atmosphere, the strong A-band (757–774 nm has long been used to estimate vertical distributions of aerosol/cloud from space. We extend this approach to include part of the O2 B-band (684–688 nm as well. SCIAMACHY onboard ENVISAT is the first instrument to provide spectral data at moderate resolution (0.2–1.5 nm in the UV/VIS/NIR including both the O2 A- and B-bands. Using SCIAMACHY specifications, we make combined use of these bands in an optimal estimation algorithm. Theoretical studies show that our algorithm is applicable both over bright and dark surfaces for the retrieval of a lognormal approximation of the vertical profile of particulate matter, in addition to its optical thickness. Synthetic studies and information content analyses prove that such a combined use provides additional information on the vertical distribution of atmospheric scatterers, attributable to differences in the absorption strengths of the two bands and their underlying surface albedos. Due to the high computational cost of the retrieval, we restrict application to real data to a case study over Kanpur through the year 2003. Comparison with AERONET data shows a commonly observed seasonal pattern of haziness, manifesting a correlation coefficient of r = 0.92 for non-monsoon monthly mean AOTs. The retrieved particulate optical thickness is found to be anti-correlated with the relative contrast of the Lambertian equivalent reflectivity (LER at 682 nm and 755 nm by a coefficient of 0.788, confirming the hypothesis made in Sanghavi et al. (2010. Our case study demonstrates a stable physics-based retrieval of particulate matter using only SCIAMACHY data. The feasibility of our approach is enhanced by the information provided by measurements around the O2 B-band in addition to the A-band. Nonetheless, operational application to SCIAMACHY data remains challenged by radiometric uncertainties, yielding simultaneous

  3. Multi-source apportionment of polycyclic aromatic hydrocarbons using simultaneous linear equations

    Science.gov (United States)

    Marinaite, Irina; Semenov, Mikhail

    2014-05-01

    A new approach to identify multiple sources of polycyclic aromatic hydrocarbons (PAHs) and to evaluate the source contributions to atmospheric deposition of particulate PAHs is proposed. The approach is based on differences in concentrations of sums of PAHs with the same molecular weight among the sources. The data on PAHs accumulation in snow as well as the source profiles were used for calculations. Contributions of aluminum production plant, oil-fired central heating boilers, and residential wood and coal combustion were calculated using the linear mixing models. The concentrations of PAH pairs such as Benzo[b]fluorantene + Benzo[k]fluorantene and Benzo[g,h,i]perylene + Indeno[1,2,3-c,d]pyrene normalized to Benzo[a]antracene + Chrysene were used as tracers in mixing equations. The results obtained using ratios of sums of PAHs were compared with those obtained using molecular diagnostic ratios such as Benzo[a]antracene/Chrysene and Benzo[g,h,i]perylene/Indeno[1,2,3-c,d]pyrene. It was shown that the results obtained using diagnostic ratios as tracers are less reliable than results obtained using ratios of sums of PAHs. Funding was provided by Siberian Branch of Russian Academy of Sciences grant No. 8 (2012-2014).

  4. Polycyclic aromatic hydrocarbon (PAH) occurrence and remediation methods

    OpenAIRE

    Henner, Pascale; Schiavon, Michel; Morel, Jean-Louis; Lichtfouse, Eric

    1997-01-01

    International audience Polycyclic aromatic hydrocarbons (PAHs) are potentially mutagenic and carcinogenic substances occurring at various concentrations in atmosphere, soils, waters and sediments. PAHs, inherited both from natural and anthropogenic processes, are persistent organic pollutants (POP) due to their chemical stability and biodegradation resistance. The increase of road transportation, and of industrial and agricultural activities has led to a notable build up of PAH amounts in ...

  5. Polarization signatures of airborne particulates

    Science.gov (United States)

    Raman, Prashant; Fuller, Kirk A.; Gregory, Don A.

    2013-07-01

    Exploratory research has been conducted with the aim of completely determining the polarization signatures of selected particulates as a function of wavelength. This may lead to a better understanding of the interaction between electromagnetic radiation and such materials, perhaps leading to the point detection of bio-aerosols present in the atmosphere. To this end, a polarimeter capable of measuring the complete Mueller matrix of highly scattering samples in transmission and reflection (with good spectral resolution from 300 to 1100 nm) has been developed. The polarization properties of Bacillus subtilis (surrogate for anthrax spore) are compared to ambient particulate matter species such as pollen, dust, and soot. Differentiating features in the polarization signatures of these samples have been identified, thus demonstrating the potential applicability of this technique for the detection of bio-aerosol in the ambient atmosphere.

  6. Polycyclic Aromatic Hydrocarbons

    Science.gov (United States)

    Salama, Farid

    2010-01-01

    Carbonaceous materials play an important role in space. Polycyclic Aromatic Hydrocarbons (PAHs) are a ubiquitous component of the carbonaceous materials. PAHs are the best-known candidates to account for the IR emission bands. They are also thought to be among the carriers of the diffuse interstellar absorption bands (DIBs). PAH ionization states reflect the ionization balance of the medium while PAH size, composition, and structure reflect the energetic and chemical history of the medium. A major challenge is to reproduce in the laboratory the physical conditions that exist in the emission and absorption interstellar zones. The harsh physical conditions of the ISM -low temperature, collisionless, strong UV radiation fields- are simulated in the laboratory by associating a molecular beam with an ionizing discharge to generate a cold plasma expansion. PAH ions and radicals are formed from the neutral precursors in an isolated environment at low temperature and probed with high-sensitivity cavity ringdown spectroscopy in the NUV-NIR range. Carbon nanoparticles are also formed during the short residence time of the precursors in the plasma and are characterized with time-offlight mass spectrometry. These experiments provide unique information on the spectra of large carbonaceous molecules and ions in the gas phase that can now be directly compared to interstellar and circumstellar observations (IR emission bands, DIBs, extinction curve). These findings also hold great potential for understanding the formation process of interstellar carbonaceous grains. We will review recent progress in the experimental and theoretical studies of PAHs, compare the laboratory data with astronomical observations and discuss the global implications.

  7. Fine airborne particulate matter: secondary production

    International Nuclear Information System (INIS)

    The chemical speciation of over 750 samples of PM2,5 collected in urban area of Milan, provides preliminary information about the role of the sources. In particular the research points out the large importance of the secondary source, i. e. the secondary production in atmosphere from gaseous precursors, that accounts for the 60- 70% of the total particulate. These findings affect the intervention policy, that must be oriented also to control the gaseous precursors of the fine particulate

  8. Externality costs by emission. E. Particulates

    International Nuclear Information System (INIS)

    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 (SO4) and nitrates (NO3), which are formed by reaction of sulfur dioxide (SO2) and nitrogen oxides (NOx) 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

  9. Environmental Behaviors and Toxicities of Polycyclic Aromatic Hydrocarbons and Nitropolycyclic Aromatic Hydrocarbons.

    Science.gov (United States)

    Hayakawa, Kazuichi

    2016-01-01

    Airborne particulate matter (PM) has been collected at four cities in Japan starting in the late 1990s, at five or more major cities in China, Korea and Russia starting in 2001 and at the Noto Peninsula starting in 2004. Nine polycyclic aromatic hydrocarbons (PAHs) and eleven nitropolycyclic aromatic hydrocarbons (NPAHs) were determined by HPLC with fluorescence and chemiluminescence detections, respectively. Annual concentrations of PAHs and NPAHs were in the order, China>Russia≫Korea=Japan, with seasonal change (winter>summer). During the observation period, concentrations of PAHs and NPAHs in Japanese cities significantly decreased but the increases in the PAH concentration were observed in Chinese and Russian cities. Concentrations of PAHs and NPAHs were higher in the Northern China than those in the Southern China. At the Noto peninsula, which is in the main path of winter northwest winds and a year-round jet stream that blow from the Asian continent to Japan, the concentrations were high in winter and low in summer every year. A cluster analysis and back trajectory analysis indicated that PAHs and NPAHs were long-range transported from Northeastern China, where coal burning systems such as coal-heating boilers are considered to be the major contributors of PAHs and NPAHs. A dramatic change in atmospheric concentrations of PAHs and NPAHs in East Asia suggests the rapid and large change of PM2.5 pollution in East Asia. Considering the adverse health effects of PM2.5, continuous monitoring of atmospheric PAHs and NPAHs is necessary in this area. PMID:26833435

  10. Polycyclic aromatic hydrocarbons, polychlorinated biphenyls, and chlorinated pesticides in background air in central Europe - investigating parameters affecting wet scavenging of polycyclic aromatic hydrocarbons

    Science.gov (United States)

    Shahpoury, P.; Lammel, G.; Holubová Šmejkalová, A.; Klánová, J.; Přibylová, P.; Váňa, M.

    2014-10-01

    Concentrations of polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and chlorinated pesticides (CPs) were measured in air and precipitation at a background site in central Europe. Σ PAH concentrations in air and rainwater ranged from 0.7 to 327.9 ng m-3 and below analytical method detection limit (particulate matter and rainwater properties were investigated. The concentrations of ionic species in particulate matter and rainwater were significantly correlated, highlighting the importance of particle scavenging process. Overall, higher scavenging efficiencies were found for relatively less volatile PAHs, underlining the effect of analyte gas-particle partitioning on scavenging process. The PAH wet scavenging was more effective when the concentrations of ionic species were high. In addition, the elemental and organic carbon contents of the particulate matter were found to influence the PAH scavenging.

  11. Monitoring Technology and Methods of Heavy Metals in Atmospheric Particulate Matter, China%中国大气颗粒物中重金属监测技术与方法综述

    Institute of Scientific and Technical Information of China (English)

    张霖琳; 薛荔栋; 滕恩江; 吕怡兵; 王业耀

    2015-01-01

    大气颗粒物中的重金属极易富集在细颗粒物中,并对人体带来危害。文章对中国大气颗粒物中重金属的监测技术方法进行梳理和汇总,从点位布设、样品采集、样品前处理、分析测试以及全过程的质量保证和质量控制等方面。探讨和分析颗粒物监测的各个环节应遵循的技术规范和相关方法。大气颗粒物的采样主要包括环境空气样品和无组织排放样品两大类,前处理方法包括全消解和酸浸提,而全消解中又包括酸消解法和碱熔法,消解方式包括电热板、马弗炉、高压密闭消解罐、微波消解等。测试方法主要包括分光光度法、X射线荧光光谱法(XRF)、原子吸收分光光度法(AAS)、原子荧光光谱法(AFS)、电感耦合等离子体发射光谱法(ICP-AES)、电感耦合等离子体质谱法(ICP-MS)等,根据不同的监测需求和仪器设备水平,选择不同的标准测试方法作为依据。在颗粒物重金属监测的全过程中,从布点、试剂空白、滤膜/滤筒空白的控制,到采样、前处理、实验室分析等各个环节,均需要考虑可能影响分析准确度的因素,建立起与监测方法同步的全程序质量保证和控制措施。完善大气颗粒物中重金属监测技术与方法体系,可为大气环境监测和管理部门的决策提供科学依据和技术支持,为源解析等颗粒物组分分析相关工作提供方法依据。%Heavy metals in atmospheric particle matters were easily enriched in PM2.5, and brought harm to human. In this paper, the Chinese monitoring technology and methods of heavy metals in ambient air particulate matters was collected sort and aggregated. All of the monitoring aspects were introduced such as sampling points laid, sample collection, sample pretreatment, sample analysis and quality assurance and quality control throughout the whole process. The technical specifications and

  12. Anthropogenic versus geogenic contribution to total suspended atmospheric particulate matter and its variations during a two-year sampling period in Beijing, China.

    Science.gov (United States)

    Schleicher, Nina; Norra, Stefan; Chai, Fahe; Chen, Yizhen; Wang, Shulan; Stüben, Doris

    2010-02-01

    Weekly samples of total suspended particles in air (TSP) were taken in south-east Beijing for a two-year period continuously from August 2005 to August 2007. Mass concentrations varied between 76 and 1028 microg m(-3) with an average concentration of 370 microg m(-3) for the whole period. The chemical composition and the mass concentration of aerosols in combination with meteorological data are reflecting specific influences of distinct aerosol sources on the pollution of Beijing's atmosphere. Lead (Pb), titanium (Ti), zinc (Zn) and copper (Cu) concentrations were chosen as indicator elements for different sources. Their amounts considerably varied over the course of the year. Element ratios, such as Pb/Ti, supported the distinction between periods of predominant geogenic or anthropogenic caused pollution. However, the interactions between aerosols from different sources are numerous and aerosol pollution still is a big and complex challenge for the sustainable development of Beijing. PMID:20145883

  13. Source Identification of Polycyclic Aromatic Hydrocarbons by Diagnostic Ratios and Positive Matrix Factorization

    Science.gov (United States)

    Dvorska, A.; Jarkovsky, J.; Lammel, G.; Klanova, J.

    2009-04-01

    by a single, well defined PAH source. By determination of the total PAH concentrations (sum of gas and particulate phases) the propagation of sampling artefacts related to PAH partitioning into statistical errors is avoided. The main results are: Major PAH source categories exhibit a significant seasonality, coronene as a marker for traffic (Bi et al., 2003) should be used with care. Long-term trends of the major PAH sources are insignificant. Literature: Bi X.H., Sheng G.Y., Peng P., Chen Y.J., Zhang Z.Q., Fu J.M., 2003. Distribution of particulate- and vapor-phase n-alkanes and polycyclic aromatic hydrocarbons in urban atmosphere of Guangzhou, China. Atmos. Environ. 37, 289-298. Paatero P. (1997): Least square formulation of robust non-negative factor analysis, Chemometrics Intelligent Lab. Systems 37, 23-35. Readman J.W., Mantoura R.F., Rhead M.M., 1987. A record of polycyclic aromatic hydrocarbon (PAH) pollution obtained from accreting sediments of the Tamar estuary, UK: evidence for non-equilibrium behaviour of PAH. Sci. Total Environ. 66, 73-94. Tauler R., Paatero P., Hopke P., Henry R.C., Spiegelman C., Park E.S., Poirot R.L., 2006. State of the art in methods and software for the identification, resolution and apportionment of contamination sources In: Summit on Environmental Modelling and Software (Proceedings of the iEMSs 3rd Biennial Meeting; Voinov A., Jakeman A.J., Rizzoli A.E., eds.), International Environmental Modelling and Software Society, Burlington, USA. WHO (2003) - World Health Organization: Health risks of persistent organic pollutants from long-range transboundary air pollution. WHO Regional Office for Europe, Copenhagen, 252 pp. Yunker M.B., Macdonald R.W., Vingarzan R., Mitchell R.H., Goyette D., Sylvestre S., 2002. PAHs in the Fraser River basin: a critical appraisal of PAH ratios as indicators of PAH source and composition. Org. Geochem. 33, 489-515.

  14. Particulate Matter (PM) Pollution

    Science.gov (United States)

    ... Environmental Protection Agency Search Search Particulate Matter (PM) Pollution Share Facebook Twitter Google+ Pinterest Contact Us Most ... issues final PM Implementation Rule Particulate Matter (PM) Pollution PM Basics What is PM, and how does ...

  15. Hourly atmospheric concentrations of Cs-134 and Cs-137 at monitoring stations for suspended particulate matter in and south of Fukushima after the Fukushima Daiichi Nuclear Power Plant accident

    Science.gov (United States)

    Tsuruta, Haruo; Oura, Yasuji; Ebihara, Mitsuru; Ohara, Toshimasa; Nakajima, Teruyuki

    2013-04-01

    No data has been found of continuous monitoring of radioactive materials in the atmosphere in Fukushima area after the Fukushima Daiichi Nuclear Power Plant (FD1NPP) accident on March 11, 2011, although it greatly contributes to accurate evaluation of the internal exposure dose, to reconstruction of emission time series of released radionuclides, and to validation of numerical simulations by atmospheric transport models. Then, we have challenged to retrieve the radioactivity in atmospheric aerosols collected every hour on a filter tape of Suspended Particulate Matter (SPM) monitoring system with beta ray attenuation method used at air pollution monitoring stations in east Japan. A test measurement for hourly atmospheric concentrations of Cs-134 and Cs-137 was successfully performed with a Ge detector for the used filter tapes during March 15-23, 2011, at three stations in Fukushima City 60 km northwest of the FD1NPP and four stations in southwest Ibaraki prefecture more than 150 km southwest of the FD1NPP. The data in Fukushima City revealed high Cs-137 concentrations of 10-30 Bq m-3 from the evening of March 15 to the early morning of March 16, when a large amount of radioactive materials was simultaneously deposited on the land surface by precipitation according to the measurement of radiation dose rate. Higher Cs-137 concentrations of 10-50 Bq m-3 were also found from the afternoon of March 20 to the morning of March 21, and which could not be detected by the radiation dose rate due to no precipitation. In contrast, much higher concentrations with the maximum of 320 Bq m-3 in southwest Ibaraki than in Fukushima City were found on the morning of March 15 and 21 under strong temperature inversion near the surface. The polluted air masses with high radioactive materials were passed away within a few hours as a plume in southwest Ibaraki, while the high Cs-137 concentrations lasted for 10-16 hours in Fukushima City where the polluted air masses after their transport

  16. Recent Trends in Atmospheric Lead Levels at an Urban-Industrial District of Metropolitan Lisbon, Portugal, through PIXE Analysis of Air-Particulate Matter

    International Nuclear Information System (INIS)

    Despite a steep decline in primary, traffic-related loads, lead in the environment is still much of an issue. Current atmospheric levels may be unmistakably reflecting the widespread use of cleaner fuels, yet decades of uncontrolled emissions from mobile sources have made lead to pervade every terrestrial (and aquatic) ecosystem, from where it keeps re-entering the lower troposphere, at least in terms of local circulation. The continuing surveillance of airborne-lead levels is thus necessary, not just for ensuring a strict compliance with regulatory decisions, but also for assisting in the implementation of remediation and/or rehabilitation policies. In Portugal, unleaded gasoline was made generally available in 1990, yet both leaded and lead-free varieties were commercialised until 1998. After that, all vehicles were compelled to use unleaded gasoline. Even though it is certainly too early for a full trend analysis of airborne levels and their response to the ban on lead, concentrations in ambient air over an important urban-industrial corridor within the Lisbon metropolitan area show a steady, sharp decrease through the last decade. Since 2000, airborne-lead data seems somewhat stabilised and, as far as busy conurbations are concerned, roughly within the values that were usually observed in the rural hinterland back in the mid 1990s

  17. Influence of in-port ships emissions to gaseous atmospheric pollutants and to particulate matter of different sizes in a Mediterranean harbour in Italy

    Science.gov (United States)

    Merico, E.; Donateo, A.; Gambaro, A.; Cesari, D.; Gregoris, E.; Barbaro, E.; Dinoi, A.; Giovanelli, G.; Masieri, S.; Contini, D.

    2016-08-01

    Ship emissions are a growing concern, especially in coastal areas, for potential impacts on human health and climate. International mitigation strategies to curb these emission, based on low-sulphur content fuels, have proven useful to improve local air quality. However, the effect on climate forcing is less obvious. Detailed information on the influence of shipping to particles of different sizes is needed to investigate air quality and climate interaction. In this work, the contributions of maritime emissions to atmospheric concentrations of gaseous pollutants (NO, NO2, SO2, and O3) and of particles (sizes from 0.009 μm to 30 μm) were investigated considering manoeuvring (arrival and departure of ships) and hotelling phases (including loading/unloading activities). Results showed that the size distributions of shipping contributions were different for the two phases and could be efficiently described, using measured data, considering four size-ranges. The largest contribution to particles concentration was observed for Dp DOAS remote sensing proved a useful tool to directly measure NO2 and SO2 ship emissions giving estimates comparable with those of emission inventory approach.

  18. The organic composition of diesel particulate matter, diesel fuel and engine oil of a non-road diesel generator.

    Science.gov (United States)

    Liang, Fuyan; Lu, Mingming; Keener, Tim C; Liu, Zifei; Khang, Soon-Jai

    2005-10-01

    Diesel-powered equipment is known to emit significant quantities of fine particulate matter to the atmosphere. Numerous organic compounds can be adsorbed onto the surfaces of these inhalable particles, among which polycyclic aromatic hydrocarbons (PAHs) are considered potential occupational carcinogens. Guidelines have been established by various agencies regarding diesel emissions and various control technologies are under development. The purpose of this study is to identify, quantify and compare the organic compounds in diesel particulate matter (DPM) with the diesel fuel and engine oil used in a non-road diesel generator. Approximately 90 organic compounds were quantified (with molecular weight ranging from 120 to 350), which include alkanes, PAHs, alkylated PAHs, alkylbenzenes and alkanoic acids. The low sulfur diesel fuel contains 61% alkanes and 7.1% of PAHs. The identifiable portion of the engine oil contains mainly the alkanoic and benzoic acids. The composition of DPM suggests that they may be originated from unburned diesel fuel, engine oil evaporation and combustion generated products. Compared with diesel fuel, DPM contains fewer fractions of alkanes and more PAH compounds, with the shift toward higher molecular weight ones. The enrichment of compounds with higher molecular weight in DPM may be combustion related (pyrogenic). PMID:16193170

  19. Characterization of atmospheric particulate matter in a museum in an urban area; Caratterizzazione del particolato aerosospeso all'interno di un museo situato in area urbana

    Energy Technology Data Exchange (ETDEWEB)

    Berico, M.; Formignani, M. [ENEA, Divisione Protezione dell' Uomo e degli Ecosistemi, Centro Ricerche Ezio Clementel, Bologna (Italy)

    2001-07-01

    In February 2001 the Internal Dosimetry Laboratory of ENEA Institute for Radioprotection carried out a measurement campaign of atmospheric aerosol in a museum, in the urban area of Bologna, in the frame of GIANO project of ENEA. The aerosol mass size distribution was measured and a high mass concentration of aerosol, 39.5 {mu}g/m{sup 3}, with an aerodynamic diameter less than 0.5 {mu}m was found. A comparison with the composition of the outdoor aerosol was made as well. In an urban area fine particles are generally generated by vehicles exhaust (particularly diesel-powered ones) and are constituted essentially of carbon black. Because of their surface adsorption properties these carbon black particles typically contain varying quantities of substances. Deposition of fine particles on the surfaces of works of art can lead to visual degradation and further damages due to chemical reactions with the adsorbed compounds. [Italian] Nell'ambito del progetto di Grafica Innovativa per il patrimonio Artistico Nazionale e per l'Occupazione Giovanile (GIANO) dell'ENEA, il laboratorio di dosimetria interna dell'Istituto per la Radioprotezione dell'ENEA, che ha competenze nella caratterizzazione fisica dell'aerosol, ha effettuato una campagna preliminare di misura del particolato aerosospeso presente all'interno di un museo nell'area urbana della citta' di Bologna. I dati dei campionamenti hanno rilevato la presenza di un'alta concentrazione in massa, 44.7 {mu}/m{sup 3}, di particolato aerosospeso inferiore a 10.5 {mu}m, composta per circa il 90%, 39.5% {mu}/m{sup 3}, da particelle con diametro aerodinamico inferiore a 0.5 {mu}m. La provenienza dalle emissioni dei motori a combustibili fossili, del particolato con queste dimensioni, ha consentito il confronto con i dati relativi alle misure di concentrazione di particolato aerosospeso effettuate presso un incrocio ad alta intensita' di traffico della citta'. Dalle

  20. Risk of human exposure to polycyclic aromatic hydrocarbons: A case study in Beijing, China

    International Nuclear Information System (INIS)

    Polycyclic aromatic hydrocarbons (PAHs) can cause adverse effects on human health. The relative contributions of their two major intake routes (diet and inhalation) to population PAH exposure are still unclear. We modeled the contributions of diet and inhalation to the overall PAH exposure of the population of Beijing in China, and assessed their human incremental lifetime cancer risks (ILCR) using a Mont Carlo simulation approach. The results showed that diet accounted for about 85% of low-molecular-weight PAH (L-PAH) exposure, while inhalation accounted for approximately 57% of high-molecular-weight PAH (H-PAH) exposure of the Beijing population. Meat and cereals were the main contributors to dietary PAH exposure. Both gaseous- and particulate-phase PAHs contributed to L-PAH exposure through inhalation, whereas exposure to H-PAHs was mostly from the particulate-phase. To reduce the cancer incidence of the Beijing population, more attention should be given to inhaled particulate-phase PAHs with considerable carcinogenic potential. - Highlights: • We modeled the contributions of diet and inhalation to population PAH exposure. • Diet contributed 85% of population exposure to low molecular-weight PAHs. • Inhalation contributed 57% of population exposure to high molecular-weight PAHs. • The PAH exposure level with body-weight adjustment decreased with age increasing. • The population cancer risk of PAH exposure is lower than the serious risk level. - The exposure of the Beijing population to carcinogenic polycyclic aromatic hydrocarbons was mainly from inhaled particulate matter

  1. Determination of Gaseous and Particulate Trifluoroacetic Acid in Atmosphere Environmental Samples by Gas Chromatography-Mass Spectrometry%大气中气相和颗粒相三氟乙酸浓度测定

    Institute of Scientific and Technical Information of China (English)

    胡瑕; 吴婧; 翟紫含; 张博雅; 张剑波

    2013-01-01

    建立了我国大气中气相和颗粒相三氟乙酸(Trifluoroacetic acid,TFA)的采集和分析方法.采用环形扩散管-滤膜联用装置分离气相和颗粒相,利用环形扩散管的碱性涂层吸附气相TFA,石英滤膜吸附颗粒相物质.对气相和颗粒相样品分别处理,以2,4-二氟苯胺作为衍生剂,与TFA反应生成TFA的苯胺产物,采用GC/MS进行分析.本方法在0.31 ~4.91μg/L浓度范围内呈线性关系(R2=0.9991),检出限为66 ng/L.采样装置回收率为(101±3)%,当采样量为48 m3,TFA大气浓度检出限为31 pg/m3.于2012年4 ~10月在北京大学采样点采集大气,测得其中TFA总浓度在501 ~ 7447 pg/m3范围,TFA在气相中的浓度大于在颗粒相中的浓度,气固分配系数Kp随温度变化.%Trifluoroacetic acid (TFA) concentration was measured in air samples by a sampling device composed of annular denuders coupled with a quartz filter,which was efficient for collection and separation of gaseous and particulate TFA.Gaseous TFA was performed by means of annular denuders coated with alkaline solution,while particulate TFA was absorbed by quartz filters.TFA can be determined by gas chromatographymass spectrometry after derivation with 2,4-difluoroaniline.Calibration curves were linear with a correlation coefficient of 0.9991.Detection limit of TFA was 66 ng/L,which was 31 pg/m3 when sampling volume was 48 m3.Recoveries of the TFA sampling device ranged between 98% and 105% with relative standard deviation (RSD) ≤ 3%.The developed method was applied for the determination of TFA in atmosphere samples collected in Peking University in Beijing in 2012.Total TFA concentrations ranged between 501 and 7447 pg/m3.Concentrations of gaseous TFA were significantly higher than those of particulate,and the gasparticle partition coefficient of TFA decreased as air temperature rose.

  2. Gas-particle partitioning and precipitation scavenging of polycyclic aromatic hydrocarbons (PAHs) in the free troposphere in southern China

    Science.gov (United States)

    Li, Peng-hui; Wang, Yan; Li, Yu-hua; Wai, Ka-ming; Li, Hong-li; Tong, Lei

    2016-03-01

    Multi-phase (gaseous, particulate and rain) samples were collected simultaneously for the first time at a high-elevation mountain site in China during March to May 2009. The site, located in the free troposphere, is used to investigate the gas-particle partitioning, precipitation scavenging of polycyclic aromatic hydrocarbons (PAHs). The total measured concentrations of 15 USEPA PAHs varied from 2.67 to 137.00 ng/m3 (average of 24.10 ng/m3). Partitioning of PAHs between gaseous and particulate phases (log Kp) was well-correlated with the supercooled liquid vapor pressure in all samples (R2 = 0.730-0.985), but the slopes (-0.154 to -0.424) were significantly deviated from the expected value of -1. The observed Kp values were better predicted by the Dual model than the Koa model, pointing to the importance of soot carbon for PAH partitioning. The scavenging ratios varied among the individual PAH compound, ranged from 4.47 × 103 (BaA) to 1.02 × 105 (ACY). Particle scavenging was the dominant removal process, accounting over 75% of the total scavenging (except for BbF) for individual PAH compound. Relationships of Wp-particle fraction, Wp-supercooled vapor pressure were analyzed. The results suggested the particle scavenging by precipitation is less efficient for PAHs with higher molecular weights, while more volatile PAHs with lower molecular weights deposited on larger atmospheric particles were scavenged more efficiently. The efficiency of Wp was found to be increased with rain intensity. For gas scavenging, the dissolution and adsorption mechanisms shift their relative importance with different supercooled vapor pressure.

  3. Refined solvable presentations for polycyclic groups

    CERN Document Server

    Hartung, René

    2011-01-01

    We announce a new type of polycyclic presentations, so-called solvable presentations, for polycyclic groups. These presentations are obtained by refining a series of normal subgroups with abelian sections. These presentations can be described effectively by presentation maps which yield the basis data structure to define a polycyclic group in computer-algebra-systems like {\\scshape Gap} or {\\scshape Magma}. We study these presentation maps and, in particular, we obtain consistency criteria for them. This consistency check has been implemented in the computer-algebra-system {\\scshape Gap}. Our implementation demonstrates that our method for solvable presentations is usually faster than the general methods for infinite polycyclic groups.

  4. Toxicological effects of polycyclic aromatic hydrocarbons and their derivatives on respiratory cells

    Science.gov (United States)

    Koike, Eiko; Yanagisawa, Rie; Takano, Hirohisa

    2014-11-01

    Polycyclic aromatic hydrocarbons (PAHs) are found in ambient aerosols and particulate matter. Experimental studies have shown that PAHs and related chemicals can induce toxicological effects. The present study aimed to investigate the effects of PAHs and their derivatives on the respiratory and immune systems and the underlying mechanisms. The human bronchial epithelial cell line BEAS-2B was exposed to PAHs and their derivatives, and the cytotoxicity and proinflammatory protein expression were then investigated. A cytotoxic effect was observed in BEAS-2B exposed to PAH derivatives such as naphthoquinone (NQ), phenanthrenequinone (PQ), 1-nitropyrene (1-NP), and 1-aminopyrene (1-AP). In addition, 1,2-NQ and 9,10-PQ showed more effective cytotoxicity than 1,4-NQ and 1,4-PQ, respectively. Pyrene showed a weak cytotoxic effect. On the other hand, naphthalene and phenanthrene showed no significant effects. Pyrene, 1-NP, and 1-AP also increased intercellular adhesion molecule-1 expression and interleukin-6 production in BEAS-2B. The increase was partly suppressed by protein kinase inhibitors such as the epidermal growth factor receptor-selective tyrosine kinase inhibitor and nuclear receptor antagonists such as the thyroid hormone receptor antagonist. The present study suggests that the toxicological effects of chemicals may be related to the different activities resulting from their structures, such as numbers of benzene rings and functional groups. Furthermore, the chemical-induced increase in proinflammatory protein expression in bronchial epithelial cells was possibly a result of the activation of protein kinase pathways and nuclear receptors. The increase may partly contribute to the adverse health effects of atmospheric PAHs.

  5. Airborne particulates. European directives and standardization; Matieres particulaires dans l`air ambiant directives europeennes et normalisation

    Energy Technology Data Exchange (ETDEWEB)

    Houdret, J.L. [Ecole Nationale Superieure des Mines, 59 - Douai (France)

    1996-12-31

    The development of future European directives concerning atmospheric dusts and particulates, organization of the in-charge committee, measurement requirements and limit value determination processes are presented. Various measuring methods and instruments used for particulate and aerosol measurements are reviewed

  6. Determination of Polycyclic Aromatic Hydrocarbons in Automobile Exhaust by Means of High-Performance Liquid Chromatography with Fluorescence Detection

    DEFF Research Database (Denmark)

    Nielsen, Tom

    1979-01-01

    A chromatographic method has been developed and applied to the determination of polycyclic aromatic hydrocarbons (PAHs) in particulate matter in automobile exhaust, in petrols, and in crankcase oils. The PAHs were purified from other organic compounds by thin-layer chromatography, separated by high......-performance liquid chromatography, and measured by means of on-line fluorescence detection. The identities of the PAHs were verified by comparing the emission spectra obtained by a stop-flow technique with those of standard PAHs...

  7. Intermolecular interactions governing the partition between particulate and gas phases for typical organic pollutants

    Institute of Scientific and Technical Information of China (English)

    YU HaiYing; QIAO XianLiang; YANG Ping; DING GuangHui; CHEN JingWen

    2007-01-01

    The partition coefficients between particulate and gas phases (Kp) for organic pollutants are of great importance to characterize the behavior of organic pollutants in atmosphere, and are basic data needed by ecological risk assessment. Partial least squares (PLS) regression with 16 theoretical molecular structural descriptors was used to develop polyparameter linear free energy relationship (LFER) model for Kp of 18 aliphatic hydrocarbons, 21 polycyclic aromatic hydrocarbons (PAHs), 16 polychlorinated biphenyls (PCBs) and 13 polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDD/Fs). The obtained model has a good predictive ability and robustness, which can be used for estimating Kp of chemicals with similar structures. Intermolecular dispersive interactions play a leading role in governing Kp, followed by charge-transfer interactions and hindrance effects of molecular size. The respective models developed for different group compounds imply that the action mechanism is similar, and dipole-dipole and dipole-induced dipole interactions play a minor role in governing Kp of n-alkanes, PCBs and PCDD/Fs.

  8. Compound-specific radiocarbon analysis of atmospheric PAH from a wood smoke-impacted city in Northern Sweden

    International Nuclear Information System (INIS)

    Full text: Atmospheric polycyclic aromatic hydrocarbons (PAHs) are ubiquitous due to their emission from a variety of combustion sources including motor vehicle exhaust and other fossil fuel combustion and biomass burning. Their potential to detrimentally impact human and ecological health makes it vital to apportion these compounds to emission sources. PAHs also have a wide range in volatility and can be present in both the gas and particulate phase in the atmosphere. However, PAHs present in high concentrations in the atmosphere are not source-specific and can be difficult to trace back to their original emission sources. Natural abundance radiocarbon analysis offers a trusted method for determining the fraction of modern versus fossil carbon and recent advances in micro-scale techniques have opened the door for compound class-specific radiocarbon analysis (CCSRA) of organic compounds at the low levels present in environmental samples. Atmospheric levels of PAHs provide a particular challenge due to difficulties in obtaining a sample with sufficient mass for radiocarbon analysis. Initial studies in Europe and Japan have shown a wide range of biomass burning contribution from 10 % of pooled PAHs for two background sites in south Europe to up to 45 % in Tokyo and 50 % at a background site in Sweden. Compound-specific radiocarbon analysis (CSRA) of atmospheric PAHs would further enhance the understanding of emission source impacts on ambient concentrations and has not been previously reported. In this study, CSRA was applied to a set of atmospheric samples collected in Lycksele, a city in Northern Sweden which has frequent episodes of severe atmospheric pollution in the winter. Previous studies carried out in the city have shown that wood combustion for residential heating has a large impact on atmospheric aerosol followed by motor vehicle emissions. This combination provided an ideal location for CSRA to apportion atmospheric PAHs between fossil fuel combustion and

  9. Relationship between polycyclic aromatic hydrocarbons (PAHs) and particle size in dated core sediments in Lake Lianhuan, Northeast China

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Li; Zang, Shuying, E-mail: zsy6311@163.com

    2013-09-01

    Atmospheric particle associated with pyrogenic polycyclic aromatic hydrocarbons (PAHs) poses serious threats to human health by inhalation exposure, especially in semiarid areas. Hence, the distributions of PAHs and particle size in two core sediments collected from Lake Lianhuan, Northeast China were studied. The sediments were dated radiometrically, and particle size distribution and PAH concentration were evaluated and potential human health risk was assessed. From 1980 to 2007, the dominant PAHs in the two cores were 2- and 3-ring PAHs, and the concentrations of 3–6 ring PAHs gradually increased from the early 1990s. Diagnostic ratios indicated that pyrogenic PAHs were the main sources of PAHs which changed over time from combustions of wood and coal to liquid fossil fuel sources. Fine particles (< 65 μm) were the predominant particle size (56–97%). Lacustrine source (with the peak towards 200–400 μm) and eolian sources derived from short (2.0–10 and 30–65 μm) and long (0.4–1.0 μm) distance suspension were indentified from frequency distribution pattern of particle size. Significant correlations between 3–6 ring PAHs (especially carcinogenic 5–6 ring PAHs) and 10–35 μm particulate fractions indicated that eolian particles played an important role in adsorbing pyrogenic PAHs. Petroleum source of PAHs was only identified during the 1980s in one core sediments, in which positive correlations between 2-ring PAHs and particulate fractions of > 125 μm were found. Future research should focus on the seven carcinogenic pyrogenic PAHs due to a rapidly increasing trend since 1995 based on the assessment of toxic equivalency factors. - Highlights: • PAHs and particle size in core sediments were used to evaluate the role of eolian particles in delivering pyrogenic PAHs. • Changes of PAH sources closely followed local historical socioeconomic development since 1980s. • Changes of particulate sources from eolian to lacustrine reflected the

  10. Toward the Complete Characterization of Atmospheric Organic Particulate Matter: Derivatization and Two-Dimensional Comprehensive Gas Chromatography/Time of Flight Mass Spectrometry as a Method for the Determination of Carboxylic Acids

    Science.gov (United States)

    Boris, Alexandra Jeanne

    Understanding the composition of atmospheric organic particulate matter (OPM) is essential for predicting its effects on climate, air quality, and health. However, the polar oxygenated fraction (PO-OPM), which includes a significant mass contribution from carboxylic acids, is difficult to speciate and quantitatively determine by current analytical methods such as gas chromatography-mass spectrometry (GC-MS). The method of chemical derivatization and two-dimensional GC with time of flight MS (GCxGC/TOF-MS) was examined in this study for its efficacy in: 1) quantifying a high percentage of the total organic carbon (TOC) mass of a sample containing PO-OPM; 2) quantitatively determining PO-OPM components including carboxylic acids at atmospherically relevant concentrations; and 3) tentatively identifying PO-OPM components. Two derivatization reagent systems were used in this study: BF3/butanol for the butylation of carboxylic acids, aldehydes, and acidic ketones, and BSTFA for the trimethylsilylation (TMS) of carboxylic acids and alcohols. Three alpha-pinene ozonolysis OPM filter samples and a set of background filter samples were collected by collaborators in a University of California, Riverside environmental chamber. Derivatization/GCxGC TOF-MS was used to tentatively identify some previously unidentified α-pinene ozonolysis products, and also to show the characteristics of all oxidation products determined. Derivatization efficiencies as measured were 40-70% for most butyl derivatives, and 50-58% for most trimethylsilyl derivatives. A thermal optical method was used to measure the TOC on each filter, and a value of the quantifiable TOC mass using a gas chromatograph was calculated for each sample using GCxGC separation and the mass-sensitive response of a flame ionization detector (FID). The TOC quantified using TMS and GCxGC-FID (TMS/TOCGCxGC FID) accounted for 15-23% of the TOC measured by the thermal-optical method. Using TMS and GCxGC/TOF-MS, 8.85% of the

  11. Polycyclic aromatic hydrocarbons with SPICA

    CERN Document Server

    Berne, O; Mulas, G; Tielens, A G G M; Goicoechea, J R

    2009-01-01

    Thanks to high sensitivity and angular resolution and broad spectral coverage, SPICA will offer a unique opportunity to better characterize the nature of polycyclic aromatic hydrocarbons (PAHs) and very small grains (VSGs), to better use them as probes of astrophysical environments. The angular resolution will enable to probe the chemical frontiers in the evolution process from VSGs to neutral PAHs, to ionized PAHs and to "Grand-PAHs" in photodissotiation regions and HII regions, as a function of G$_0$/n (UV radiation field / density). High sensitivity will favor the detection of the far-IR skeletal emission bands of PAHs, which provide specific fingerprints and could lead to the identification of individual PAHs. This overall characterization will allow to use PAH and VSG populations as tracers of physical conditions in spatially resolved protoplanetary disks and nearby galaxies (using mid-IR instruments), and in high redshift galaxies (using the far-IR instrument), thanks to the broad spectral coverage SPIC...

  12. Advanced Hybrid Particulate Collector Project Management Plan

    Energy Technology Data Exchange (ETDEWEB)

    Miller, S.J.

    1995-11-01

    As the consumption of energy increases, its impact on ambient air quality has become a significant concern. Recent studies indicate that fine particles from coal combustion cause health problems as well as atmospheric visibility impairment. These problems are further compounded by the concentration of hazardous trace elements such as mercury, cadmium, selenium, and arsenic in fine particles. Therefore, a current need exists to develop superior, but economical, methods to control emissions of fine particles. Since most of the toxic metals present in coal will be in particulate form, a high level of fine- particle collection appears to be the best method of overall air toxics control. However, over 50% of mercury and a portion of selenium emissions are in vapor form and cannot be collected in particulate control devices. Therefore, this project will focus on developing technology not only to provide ultrahigh collection efficiency of particulate air toxic emissions, but also to capture vapor- phase trace metals such as mercury and selenium. Currently, the primary state-of-the-art technologies for particulate control are fabric filters (baghouses) and electrostatic precipitators (ESPs). However, they both have limitations that prevent them from achieving ultrahigh collection of fine particulate matter and vapor-phase trace metals. The objective of this project is to develop a highly reliable advanced hybrid particulate collector (AHPC) that can provide > 99.99 % particulate collection efficiency for all particle sizes between 0.01 and 50 14m, is applicable for use with all U.S. coals, and is cost-0443competitive with existing technologies. Phase I of the project is organized into three tasks: Task I - Project Management, Reporting, and Subcontract Consulting Task 2 - Modeling, Design, and Construction of 200-acfm AHPC Model Task 3 - Experimental Testing and Subcontract Consulting

  13. 40 CFR 60.122 - Standard for particulate matter.

    Science.gov (United States)

    2010-07-01

    ... subpart shall discharge or cause the discharge into the atmosphere from a blast (cupola) or reverberatory furnace any gases which: (1) Contain particulate matter in excess of 50 mg/dscm (0.022 gr/dscf). (2... shall discharge or cause the discharge into the atmosphere from any pot furnace any gases which...

  14. The biocatalyzed stereoselective preparation of polycyclic cyanohydrins

    OpenAIRE

    Silva, M. Manuel Cruz; Melo, M. Luísa Sá e; Parolin, Marco; Tessaro, Davide; Riva, Sergio; Danieli, Bruno

    2004-01-01

    The enzyme-mediated preparation of enantiomerically or diastereomerically enriched polycyclic cyanohydrins has been investigated. Oxynitrilase-catalyzed cyanurations gave excellent results with the bicyclic aldehydes tested. On the other hand, enantio- or diastereoselective acylation, catalyzed by lipase PS or subtilisin, proved to be a more versatile methodology, giving good results even with sterically hindered polycyclic cyanohydrins. Specifically, the steroidal cyanohydrin derivative 4b w...

  15. Refined solvable presentations for polycyclic groups

    Directory of Open Access Journals (Sweden)

    René Hartung

    2012-06-01

    Full Text Available We describe a new type of presentation that, when consistent, describes a polycyclic group. This presentation is obtained by re ning a series of normal subgroups with abelian sections. These presentations can be described e ectively in computeralgebra- systems like Gap or Magma. We study these presentations and, in particular, we obtain consistency criteria for them. The consistency implementation demonstrates that there are situations where the new method is faster than the existing methods for polycyclic groups.

  16. Atmospheric Light Detection and Ranging (LiDAR) Coupled With Point Measurement Air Quality Samplers to Measure Fine Particulate Matter (PM) Emissions From Agricultural Operations: The Los Banos CA Fall 2007 Tillage Campaign.

    Science.gov (United States)

    Airborne particles, especially fine particulate matter 2.5 micrometers (μm) or less in aerodynamic diameter (PM2.5), are microscopic solids or liquid droplets that can cause serious health problems, including increased respiratory symptoms such as coughing or difficulty breathing...

  17. Mechanistic and kinetic studies on the OH-initiated atmospheric oxidation of fluoranthene

    International Nuclear Information System (INIS)

    The atmospheric oxidation of polycyclic aromatic hydrocarbons (PAHs) can generate toxic derivatives which contribute to the carcinogenic potential of particulate organic matter. In this work, the mechanism of the OH-initiated atmospheric oxidation of fluoranthene (Flu) was investigated by using high-accuracy molecular orbital calculations. All of the possible oxidation pathways were discussed, and the theoretical results were compared with the available experimental observation. The rate constants of the crucial elementary reactions were evaluated by the Rice–Ramsperger–Kassel–Marcus (RRKM) theory. The main oxidation products are a range of ring-retaining and ring-opening chemicals containing fluoranthols, fluoranthones, fluoranthenequinones, nitro-fluoranthenes, dialdehydes and epoxides. The overall rate constant of the OH addition reaction is 1.72 × 10−11 cm3 molecule−1 s−1 at 298 K and 1 atm. The atmospheric lifetime of Flu determined by OH radicals is about 0.69 days. This work provides a comprehensive investigation of the OH-initiated oxidation of Flu and should help to clarify its atmospheric conversion. - Highlights: • We studied a comprehensive mechanism of OH-initiated oxidation of fluoranthene. • We reported the formation pathways of fluoranthone, fluoranthenequinone and epoxide. • The rate constants of the crucial elementary steps were evaluated

  18. Mechanistic and kinetic studies on the OH-initiated atmospheric oxidation of fluoranthene

    Energy Technology Data Exchange (ETDEWEB)

    Dang, Juan; Shi, Xiangli; Zhang, Qingzhu, E-mail: zqz@sdu.edu.cn; Hu, Jingtian; Chen, Jianmin; Wang, Wenxing

    2014-08-15

    The atmospheric oxidation of polycyclic aromatic hydrocarbons (PAHs) can generate toxic derivatives which contribute to the carcinogenic potential of particulate organic matter. In this work, the mechanism of the OH-initiated atmospheric oxidation of fluoranthene (Flu) was investigated by using high-accuracy molecular orbital calculations. All of the possible oxidation pathways were discussed, and the theoretical results were compared with the available experimental observation. The rate constants of the crucial elementary reactions were evaluated by the Rice–Ramsperger–Kassel–Marcus (RRKM) theory. The main oxidation products are a range of ring-retaining and ring-opening chemicals containing fluoranthols, fluoranthones, fluoranthenequinones, nitro-fluoranthenes, dialdehydes and epoxides. The overall rate constant of the OH addition reaction is 1.72 × 10{sup −11} cm{sup 3} molecule{sup −1} s{sup −1} at 298 K and 1 atm. The atmospheric lifetime of Flu determined by OH radicals is about 0.69 days. This work provides a comprehensive investigation of the OH-initiated oxidation of Flu and should help to clarify its atmospheric conversion. - Highlights: • We studied a comprehensive mechanism of OH-initiated oxidation of fluoranthene. • We reported the formation pathways of fluoranthone, fluoranthenequinone and epoxide. • The rate constants of the crucial elementary steps were evaluated.

  19. Characterisation of carbonaceous particulate matter in Edinburgh

    OpenAIRE

    Hammonds, Mark David

    2012-01-01

    Airborne particulate matter (PM) has important harmful effects on human health, as well as a number of other important atmospheric effects. Although progress has been made in understanding the sources and effects of PM, there remains considerable uncertainty on a number of issues, including the nature of a lot of the carbonaceous material, which comprises 30{50% on average of PM mass. This project aims to compare different methods of PM measurement, and contribute understanding...

  20. Spatial distribution of polycyclic aromatic hydrocarbons in Terminalia catappa L. (Combretaceae) bark from a selected heavy road traffic area of Rio de Janeiro City, Brazil.

    Science.gov (United States)

    Pereira Netto, Annibal D; Barreto, Renata P; Moreira, Josino C; Arbilla, Graciela

    2007-04-01

    The levels of 21 polycyclic aromatic hydrocarbons (PAHs) with molecular weights between 128 Da (naphthalene) and 300 Da (coronene) were determined in Terminalia catappa L. (Combretaceae) bark. Tree bark samples were collected in the campus of Oswaldo Cruz Foundation, a green area located in a very intensive traffic area of Rio de Janeiro City, Brazil and about 10 km away from the city center. Samples were submitted to ultrasonic extraction with dichloromethane and analyzed by high-resolution gas chromatography-mass spectrometry. Individual PAH levels varied from 1.23 to 327 ng/g and phenanthrene, fluoranthene and pyrene predominated in all samples. Total PAH levels ranged from 242 to 1640 ng/g with a mean of 628 ng/g. The levels of total PAHs and of total carcinogenic PAHs showed not a clear dependence with tree location and distances to the main routes of that area. No correlation was observed also with PAH levels previously found in total suspended particulate thus indicating that in this area tree bark PAH levels cannot be used to assess their atmospheric levels. PMID:17010512

  1. Characterization of functional groups of airborne particulate matter

    International Nuclear Information System (INIS)

    Particulate matter of organic combustibles burning consists of various hydrocarbons and radicals, which may cause harmful impact to human health. In this study solid particulate matter were collected on the filters from burning of various combustibles in a burning chamber and from atmosphere of city of Riga by dichotomous impactor. FTIR spectra were obtained before and after samples' treatment. Absorptions associated with aliphatic and aromatic hydrocarbons and alcohol functional groups were observed in the FTIR spectra. Free radicals of particulate matter were detected by electron paramagnetic resonance (EPR)

  2. Composition and effects of inhalable size fractions of atmospheric aerosols in the polluted atmosphere: part I. PAHs, PCBs and OCPs and the matrix chemical composition.

    Science.gov (United States)

    Landlová, Linda; Cupr, Pavel; Franců, Juraj; Klánová, Jana; Lammel, Gerhard

    2014-05-01

    Atmospheric particulate matter (PM) abundance, mass size distribution (MSD) and chemical composition are parameters relevant for human health effects. The MSD and phase state of semivolatile organic pollutants were determined at various polluted sites in addition to the PM composition and MSD. The distribution pattern of pollutants varied from side to side in correspondence to main particle sources and PM composition. Levels of particle-associated polycyclic aromatic hydrocarbons (PAHs) were 1-30 ng m(-3) (corresponding to 15-35 % of the total, i.e., gas and particulate phase concentrations), of polychlorinated biphenyls (PCBs) were 2-11 pg m(-3) (4-26 % of the total) and of DDT compounds were 2-12 pg m(-3) (4-23 % of the total). The PM associated amounts of other organochlorine pesticides were too low for quantification. The organics were preferentially found associated with particles contaminants and toxicological effects occur. Legislative regulation based on gravimetric determination of PM mass can clearly be insufficient for assessment. PMID:24488522

  3. Activation analysis of air particulate matter

    International Nuclear Information System (INIS)

    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)

  4. Particle size distribution of nitrated and oxygenated polycyclic aromatic hydrocarbons (NPAHs and OPAHs on traffic and suburban sites of a European megacity: Paris (France

    Directory of Open Access Journals (Sweden)

    J. Ringuet

    2012-09-01

    Full Text Available The size distribution of particulate nitrated and oxygenated polycyclic aromatic hydrocarbons (NPAHs and OPAHs was determined during two field campaigns at a traffic site in summer 2010 and at a suburban site during the MEGAPOLI (Megacities: Emissions, urban, regional and Global Atmospheric POLlution and climate effects, and Integrated tools for assessment and mitigation experiment in summer 2009. Both, OPAHs and NPAHs were strongly associated (>85% to fine particles (Dp< 2.5 μm increasing the interest of their study on a sanitary point of view. Results showed really different NPAH and OPAH particle size distributions between both sites. At traffic site, clearly bimodal (notably for NPAHs particle size distributions (Dp = 0.14 and 1.4 μm were observed, while the particle size distributions were more scattered at the suburban site, especially for OPAHs. Bimodal particle size distribution observed at traffic site for the NPAH could be assigned to the vehicle emissions and the particle resuspension. Broadest distribution observed at the suburban site could be attributed to the mass transfer of compounds by volatilization/sorption processes during the transport of particles in the atmosphere. Results also showed that the combination of the study of particle size distributions applied to marker compounds (primary: 1-nitropyrene; secondary: 2-nitrofluoranthene and to NPAH or OPAH chemical profiles bring some indications on their primary and/or secondary origin. Indeed, 1,4-anthraquinone seemed only primary emitted by vehicles while 7-nitrobenz[a]anthracene, benz[a]antracen7,12-dione and benzo[b]fluorenone seemed secondarily formed in the atmosphere.

  5. Deuterated polycyclic aromatic hydrocarbons: Revisited

    CERN Document Server

    Doney, Kirstin D; Mori, Tamami; Onaka, Takashi; Tielens, A G G M

    2016-01-01

    The amount of deuterium locked up in polycyclic aromatic hydrocarbons (PAHs) has to date been an uncertain value. We present a near-infrared (NIR) spectroscopic survey of HII regions in the Milky Way, Large Magellanic Cloud (LMC), and Small Magellanic Cloud (SMC) obtained with AKARI, which aims to search for features indicative of deuterated PAHs (PAD or Dn-PAH) to better constrain the D/H ratio of PAHs. Fifty-three HII regions were observed in the NIR (2.5-5 {\\mu}m), using the Infrared Camera (IRC) on board the AKARI satellite. Through comparison of the observed spectra with a theoretical model of deuterated PAH vibrational modes, the aromatic and (a)symmetric aliphatic C-D stretch modes were identified. We see emission features between 4.4-4.8 {\\mu}m, which could be unambiguously attributed to deuterated PAHs in only six of the observed sources, all of which are located in the Milky Way. In all cases, the aromatic C-D stretching feature is weaker than the aliphatic C-D stretching feature, and, in the case o...

  6. PROTONATED POLYCYCLIC AROMATIC HYDROCARBONS REVISITED

    International Nuclear Information System (INIS)

    We reconsider the contribution that singly protonated polycyclic aromatic hydrocarbons (PAHs; HPAH+s) might make to the Class A component of the 6.2 μm interstellar emission feature in light of the recent experimental measurements of protonated naphthalene and coronene. Our calculations on the small HPAH+s have a band near 6.2 μm, as found in experiment. While the larger HPAH+s still have emission near 6.2 μm, the much larger intensity of the band near 6.3 μm overwhelms the weaker band at 6.2 μm, so that the 6.2 μm band is barely visible. Since the large PAHs are more representative of those in the interstellar medium, our work suggests that large HPAH+s cannot be major contributors to the observed emission at 6.2 μm (i.e., Class A species). Saturating large PAH cations with hydrogen atoms retains the 6.2 μm Class A band position, but the rest of the spectrum is inconsistent with observed spectra.

  7. Distribution of Polycyclic aromatic hydrocarbons between water, sediment and common eels (Anguilla angillae) in the urban stretch of Tevere River

    International Nuclear Information System (INIS)

    The research has focused the attention on the occurrence of polycyclic aromatic hydrocarbons (PAHs) in water, sediment and common eels (Angilla anguillae) in the urban area of Tevere River. These compounds can derived from point (E.g.oil spill) or non-point (e.g. atmospheric deposition) sources and are one of the most widespread organic pollutants. (Author)

  8. Univers de Particules

    CERN Multimedia

    CERN Video Productions

    2010-01-01

    Dans l’Univers, tout est fait de particules. Mais d’où viennent-elles? Quelle est l’origine des lois de la nature? Au rez-de-chaussée du Globe de la science et de l’innovation, l’exposition permanente « Univers de particules » vous invite à un voyage vers le Big Bang en explorant le CERN. Avec à la clé des réponses aux questions: pourquoi cette recherche ? Comment accélérer des particules ? Comment les détecter ? Quelles sont les théories sur la matière et sur l’Univers aujourd’hui ? Quelles retombées pour notre vie quotidienne ?

  9. Patterns and sources of particle-phase aliphatic and polycyclic aromatic hydrocarbons in urban and rural sites of western Greece

    Science.gov (United States)

    Kalaitzoglou, Maria; Terzi, Eleni; Samara, Constantini

    Particle-bound aliphatic and polycyclic aromatic hydrocarbons (AHs and PAHs, respectively) were determined in the ambient air of the Eordea basin, in western Greece, where intensive coal burning for power generation takes place. Thirteen PAHs, n-alkanes (C 14-C 35), hopanes, and isoprenoid hydrocarbons (pristane and phytane) were determined in the total suspended particles collected from the atmosphere of four sites within the basin receiving potential impacts from various sources, such as fly ash, coal mining, automobile traffic, domestic heating, and agricultural or refuse burning. The same organic species were also determined in the fly ash generated in power stations, and in particulate emissions from open burning of biomass (dry corn leaves) and refuse burning. Organic particle sources were resolved using concentration diagnostic ratios and factor analysis (FA). A multivariate statistical receptor model (Absolute Principal Component Analysis, APCA) was finally employed to estimate the contribution of identified sources to the measured concentrations of organic pollutants. Four major sources for ambient PAHs and AHs were identified displaying variable contribution in different sites: (a) fossil fuel combustion, (b) biogenic emissions, (c) refuse burning, and (d) oil residues. Fuel combustion was the major source of ambient PAHs and an important source of n-alkanes in the range C 21-C 28. Oil residues were found to be the major source of low molecular weight n-alkanes (particularly the C 14-C 16), and an important source of pristane, phytane and UCM. Biogenic sources were primarily responsible for the high molecular weight n-alkanes explaining almost the entire concentration levels of homologues >C 32. Biomass burning was particularly important for the C 23-C 26n-alkanes. Despite the vicinity of certain sampling sites to power stations, coal fly ash was not identifiable as a source for ambient PAHs and AHs.

  10. Patterns and sources of particle-phase aliphatic and polycyclic aromatic hydrocarbons in urban and rural sites of western Greece

    Energy Technology Data Exchange (ETDEWEB)

    Kalaitzoglou, M.; Terzi, E.; Samara, C. [Aristotle University, Thessaloniki (Greece). Dept. of Chemistry

    2004-05-01

    Particle-bound aliphatic and polycyclic aromatic hydrocarbons (AHs and PAHs, respectively) were determined in the ambient air of the Eordea basin, in western Greece, where intensive coal burning for power generation takes place. Thirteen PAHs, n-alkanes (C{sub 14}-C{sub 35}), hopanes, and isoprenoid hydrocarbons (pristane and phytane) were determined in the total suspended particles collected from the atmosphere of four sites within the basin receiving potential impacts from various sources, such as fly ash, coal mining, automobile traffic, domestic heating, and agricultural or refuse burning. The same organic species were also determined in the fly ash generated in power stations, and in particulate emissions from open burning of biomass (dry corn leaves) and refuse burning. Organic particle sources were resolved using concentration diagnostic ratios and factor analysis (FA). A multivariate statistical receptor model Absolute Principal Component Analysis (APCA), was finally employed to estimate the contribution of identified sources to the measured concentrations of organic pollutants. Four major sources for ambient PAHs and AHs were identified displaying variable contribution in different sites: (a) fossil fuel combustion, (b) biogenic emissions, (c) refuse burning, and (d) oil residues. Fuel combustion was the major source of ambient PAHs and an important source of n-alkanes in the range C{sub 21}-C{sub 28}. Oil residues were found to be the major source of low molecular weight n-alkanes (particularly the C{sub 14}-C{sub 16}), and an important source of pristane, phytane and UCM. Biogenic sources were primarily responsible for the high molecular weight n-alkanes explaining almost the entire concentration levels of homologues >C{sub 32}. Biomass burning was particularly important for the C{sub 23}-C{sub 26} n-alkanes. Despite the vicinity of certain sampling sites to power stations, coal fly ash was not identifiable as a source for ambient PAHs and AHs. (author)

  11. Microwave regenerated particulate trap

    Energy Technology Data Exchange (ETDEWEB)

    McDonald, A.C. Jr.; Yonushonis, T.M. [Cummins Engine Co., Inc., Columbus, IN (United States); Haberkamp, W.C.; Mako, F.; Len, L.K,; Silberglitt, R.; Ahmed, I. [FM Technologies, Inc., Fairfax, VA (United States)

    1997-12-31

    It has been demonstrated that a fibrous particulate filter can extract particulate matter from the diesel exhaust. However, additional engineering efforts remains to achieve the design target of 90%. It has also be shown that with minor modifications magnetrons produced for home ovens can endure a simulated diesel operating environment. Much work remains to develop a robust product ready to complete extensive engine testing and evaluation. These efforts include: (1) additional environmental testing of magnetrons; (2) vibration testing of the filter in the housing; (3) evaluating alternative methods/designs to seal the center bore; and (4) determining the optimum coating thickness that provides sufficient structural integrity while maintaining rapid heating rates.

  12. Simulation of the propagation and deposition of polycyclic aromatic hydrocarbons for a winter-time period in Baden-Wuerttemberg; Simulation der Ausbreitung und Deposition von polyzyklischen aromatischen Kohlenwasserstoffen fuer eine Winterepisode in Baden-Wuerttemberg

    Energy Technology Data Exchange (ETDEWEB)

    Nester, K. [Forschungzentrum Karlsruhe (Germany). Inst. fuer Meteorologie und Klimaforschung

    1997-12-31

    Polycyclic aromatic hydrocarbons (PAHs) belong to the group of environmentally hazardous substances because of their cancerogenous effect. They occur both as gases and in particulate form and are released by man into the atmosphere as combustion products. They play a role not only in the atmosphere but also in soil. An essential process permitting these substances to penetrate into the soil is by deposition from the atmosphere.- The study had the aim of assessing atmospheric PAH deposition to the soil. The outcome is used to simulate PAH behaviour in soil, a task which also forms part of the interlaboratory project `soil`. As PAHs are regularly measured only in a few places, PAH transfer from atmosphere to soil needs to be numerically modelled. That the model can do this was first of all to be demonstrated for a short period. The result is described in the paper. Subsequently, statements regarding long-term PAH transfer are attempted. (orig.) [Deutsch] Die Polycyklischen Aromatischen Kohlenwasserstoffe (PAK) gehoeren wegen ihrer kanzerogenen Wirkungen zu den umweltbelastenden Substanzen. Sie treten sowohl als Gase als auch als Partikel auf und werden antropogen als Verbrennungsprodukte in die Atmosphaere freigesetzt. Neben ihrer Wirkung in der Atmosphaere spielen sie im Boden eine Rolle. Ein wesentlicher Prozess, der diese Substanzen in den Boden gelangen laesst, ist die Deposition aus der Atmosphaere zum Boden. Ziel der Untersuchungen war es, den atmosphaerischen Eintrag der PAK in den Boden zu bestimmen. Dieser Eintrag dient der Simulation des Verhaltens der PAK im Boden, der ebenfalls Bestandteil des Verbundprojekts `Boden` war. Da es nur wenige Stellen gibt, an denen regelmaessig PAK`s gemessen werden, ist es notwendig, den PAK Eintrag aus der Atmosphaere zum Boden mittels Modellrechnungen abzuschaetzen. Dabei sollte zunaechst fuer eine kurze Episode gezeigt werden, dass das Modell in der Lage ist, dies zu leisten. Dieses Ergebnis wird im folgenden vorgestellt

  13. Temporal variability of Polycyclic Aromatic Hydrocarbons in a receptor site of Puebla -Tlaxcala Valley.

    Science.gov (United States)

    Padilla Barrera, Zuhelen; Torres Jardón, Ricardo; Gerardo Ruiz, Luis; Castro, Telma

    2015-04-01

    The Puebla-Tlaxcala Valley is a region with high population scattered over two states, where emissions from combustion of a variety of materials and fuels represent a major problem in the deterioration of air quality. Polycyclic aromatic hydrocarbons (PAHs) are a class of semi-volatile organic compounds that are formed during combustion. PAH are present in large amounts in the particulate matter comes from the combustion and no combustion. The particle-bound PAHs are formed by accumulation and condensation mechanisms in the particle. In its condensed form are mainly associated with fine particles (converter, and once emitted into the atmosphere, particulate PAHs may undergo transformation by photo-oxidation. The measurements were made with a photoelectric aerosol sensor (PAS 2000 CE) and a diffusion charger (DC 2000 CE), the first determines the concentration of PAHs, while the second determines the active surface of particles. The use of these two sensors in parallel is a useful tool to identify quantitatively the greatest source of emission, describe the physical and chemical characteristics of the particles. Correlations between PAHs with the active surface (DC), NOy and CO, together with an analysis of weather atmospheric transport to approximate the possible origin of these particles. The coefficient PAHs / DC associated with the backward trajectory analysis is a tool to identify potential areas of emission. The correlation between PAHs and NOx reflects emissions associated with diesel combustion, while the correlation between PAHs and CO, combustion of gasoline. Concentration patterns were recorded over 24 hours in both PAHs and DC. The average concentration of PAHs was 4.9 ng/m3 and the maximum of 81.9 ng/m3 , while the average active surface area was 81.9 mm2/m3and the maximum of 176.8 mm2/m3. Peak concentrations occurred at dawn and in the early hours of the morning then decreasing in the morning and evening. Particularly notable was the drop in the

  14. Alkyl polycyclic aromatic hydrocarbons emissions in diesel/biodiesel exhaust

    Science.gov (United States)

    Casal, Carina S.; Arbilla, Graciela; Corrêa, Sergio M.

    2014-10-01

    Polycyclic aromatic hydrocarbons (PAHs) are widely studied in environmental matrices, such as air, water, soil and sediment, because of their toxicity, mutagenicity and carcinogenicity. Because of these properties, the environmental agencies of developed countries have listed sixteen PAHs as priority pollutants. Few countries have limits for these compounds for ambient air, but they only limit emissions from stationary and mobile sources and occupational areas. There are several studies to specifically address the 16 priority PAHs and very little for the alkyl PAHs. These compounds are more abundant, more persistent and frequently more toxic than the non-alkylated PAHs, and the toxicity increases with the number of alkyl substitutions on the aromatic ring. In this study, a method was developed for the analysis of PAHs and alkyl PAHs by using a GC-MS and large injection volume injection coupled with program temperature vaporisation, which allows for limits of detection below 1.0 ng μL-1. Several variables were tested, such as the injection volume, injection velocity, injector initial temperature, duration of the solvent split and others. This method was evaluated in samples from particulate matter from the emissions of engines employing standard diesel, commercial diesel and biodiesel B20. Samples were collected on a dynamometer bench for a diesel engine cycle and the results ranged from 0.5 to 96.9 ng mL-1, indicating that diesel/biodiesel makes a significant contribution to the formation of PAHs and alkyl PAHs.

  15. Multiphoton ionization mass spectrometry of nitrated polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Tang, Yuanyuan; Imasaka, Tomoko; Yamamoto, Shigekazu; Imasaka, Totaro

    2015-08-01

    In order to suppress the fragmentation and improve the sensitivity for determination of nitrated polycyclic aromatic hydrocarbons (NPAHs), the mechanism of multiphoton ionization was studied for the following representative NPAHs, 9-nitroanthracene, 3-nitrofluoranthene, and 1-nitropyrene. The analytes were extracted from the PM2.5 on the sampling filter ultrasonically, and were measured using gas chromatography/multiphoton ionization/time-of-flight mass spectrometry with a femtosecond tunable laser in the range from 267 to 405 nm. As a result, a molecular ion was observed as the major ion and fragmentation was suppressed at wavelengths longer than 345 nm. Furthermore, the detection limit measured at 345 nm was measured to be the subpicogram level. The organic compounds were extracted from a 2.19 mg sample of particulate matter 2.5 (PM2.5), and the extract was subjected to multiphoton ionization mass spectrometry after gas chromatograph separation. The background signals were drastically suppressed at 345 nm, and the target NPAHs, including 9-nitroanthracene and 1-nitropyrene, were detected, and their concentrations were determined to be 5 and 3 pg/m(3), respectively. PMID:26048831

  16. Impact of the Improved Patsari Biomass Stove on Urinary Polycyclic Aromatic Hydrocarbon Biomarkers and Carbon Monoxide Exposures in Rural Mexican Women

    OpenAIRE

    Riojas-Rodriguez, Horacio; Schilmann, Astrid; Marron-Mares, Adriana Teresa; Masera, Omar; Li, Zheng; Romanoff, Lovisa; Sjödin, Andreas; Rojas-Bracho, Leonora; Needham, Larry L.; Romieu, Isabelle

    2011-01-01

    Background: Cooking with biomass fuels on open fires results in exposure to health-damaging pollutants such as carbon monoxide (CO), polycyclic aromatic hydrocarbons (PAHs), and particulate matter. Objective: We compared CO exposures and urinary PAH biomarkers pre- and postintervention with an improved biomass stove, the Patsari stove. Methods: In a subsample of 63 women participating in a randomized controlled trial in central Mexico, we measured personal CO exposure for 8 hr during the day ...

  17. Diurnal variability of polycyclic aromatic compound (PAC) concentrations: Relationship with meteorological conditions and inferred sources

    Science.gov (United States)

    Alam, Mohammed S.; Keyte, Ian J.; Yin, Jianxin; Stark, Christopher; Jones, Alan M.; Harrison, Roy M.

    2015-12-01

    Polycyclic aromatic hydrocarbons (PAH) and their nitro and oxy derivatives have been sampled every three hours over one week in winter at two sites in Birmingham UK. One site is heavily influenced by road traffic and is close to residential dwellings, while the other site is a background urban location at some distance from both sources of emission. The time series of concentrations has been examined along with the ratio of concentrations between the two sampling sites. A comparison of averaged diurnal profiles has shown different patterns of behaviour which has been investigated through calculating ratios of concentration at 18:00-21:00 h relative to that at 06:00-09:00 h. This allows identification of those compounds with a strong contribution to a traffic-related maximum at 06:00-09:00 h which are predominantly the low molecular weight PAHs, together with a substantial group of quinones and nitro-PAHs. Changes in partitioning between vapour and particulate forms are unlikely to influence the ratio as the mean temperature at both times was almost identical. Most compounds show an appreciable increase in concentrations in the evening which is attributed to residential heating emissions. Compounds dominated by this source show high ratios of 18:00-21:00 concentrations relative to 06:00-09:00 concentrations and include higher molecular weight PAH and a substantial group of both quinones and nitro-PAH. The behaviour of retene, normally taken as an indicator of biomass burning, is suggestive of wood smoke only being one contributor to the evening peak in PAH and their derivatives, with coal combustion presumably being the other main contributor. Variations of PAH concentrations with wind speed show a dilution behaviour consistent with other primary pollutants, and high concentrations of a range of air pollutants were observed in an episode of low temperatures and low wind speeds towards the end of the overall sampling period consistent with poor local dispersion

  18. Regional-scale simulation of transport and transformations of semi-volatile polycyclic aromatic hydrocarbons (PAHs) in East Asia: diurnal variations investigation

    Science.gov (United States)

    Mu, Qing; Lammel, Gerhard; Cheng, Yafang

    2015-04-01

    Semi-volatile PAHs are major pollutants of urban air, mostly regionally transported and reaching remote environments[1]. Some semi-volatile PAHs are carcinogenic. About 22% of global PAHs emissions are in China. The transport and sinks (atmospheric reactions, deposition) of semi-volatile PAHs in East Asia are studied using a modified version of the Weather Research and Forecasting model coupled with chemistry (WRF/Chem [2]). For this purpose, PAHs' gas and particulate phase chemical reactions and dry and wet deposition processes are included. We use emissions of 2008 [3] which include technical combustion processes (coal, oil, gas, waste and biomass) and open fires and apply diurnal time functions as those of black carbon. The model was run for phenanthrene (3-ring PAH, p = 1.5×10-2 Pa at 298 K) and benzo(a)pyrene (5-ring PAH, p = 7×10-7 Pa) for July 2013 with hourly output and 27 km horizontal grid spacing. The comparison of model predicted phenanthrene concentrations with measurements at a rural site near Beijing (own data, unpublished) validates the model's ability to simulate diurnal variations of gaseous PAHs. The model's performance is better in simulating day time than night time gaseous PAHs. The concentrations of PAHs had experienced significant diurnal variations in rural and remote areas of China. Elevated concentration levels of 40-60 ng m-3 for phenanthrene and 1-10 ng m-3 for benzo(a)pyrene are predicted in Shanxi, Guizhou, the North China Plain, the Sichuan Basin and Chongqing metropolitan areas due to the high emission densities at those locations. References [1] Keyte, I.J., Harrison, R.M., and Lammel, G., 2013: Chemical reactivity and long-range transport potential of polycyclic aromatic hydrocarbons - a review, Chem. Soc. Rev., 42, 9333-9391. [2] Grell, G.A, Peckham, S.E, Schmitz, R, McKeen, S.A, Frost, G, Skamarock, W.C, and Eder, B., 2005: Fully coupled online chemistry within the WRF model, Atmos. Environ., 39, 6957-6975. [3] Shen, H. Z

  19. Composition of semi-volatile organic compounds in the urban atmosphere of Singapore: influence of biomass burning

    Directory of Open Access Journals (Sweden)

    J. He

    2010-04-01

    Full Text Available An intensive field study was conducted in the urban atmosphere of Singapore to investigate the composition of organic compounds in both gaseous and particulate phases during the period of August to early November 2006. 17 atmospheric samples were collected. These samples were subjected to accelerated solvent extraction with a mixture of dichloromethane and acetone and separated into functional group fractions for analyses by GC/MS. Over 180 organic compounds belonging to three major fractions (n-alkanes, polycyclic aromatic hydrocarbons (PAHs, and polar organic compounds (POCs were identified and quantified. The characteristics and abundance of the n-alkanes, PAHs, mono and dicarboxylic acids, methoxylated phenols and other POCs were determined. The composition of these organic compounds fluctuated temporally with most of them being relatively higher in October than those in other months of the sampling period. 3-D backward air mass trajectory analyses together with the carbon preference index (CPI, molecular diagnostic ratios and molecular markers were used to investigate the origin of organic species measured in this study. Based on these diagnostic tools, the increased abundance of atmospheric organic species during October could be attributed to the occurrence of regional smoke haze episodes due to biomass burning in Indonesia. Among the POCs investigated, phthalic acid and cis-pinonic acid showed a strong linear relationship with maximum daily ozone concentration, indicating secondary organic aerosols (SOA to be an important contributor to ambient atmospheric organics over Singapore.

  20. Toxicity to chicken embryos of organic extracts from airborne particulates separated into five sizes

    Energy Technology Data Exchange (ETDEWEB)

    Matsumoto, H.

    1988-07-01

    The chicken embryo assay has been used for research on the toxicity of complex extracts derived from different environmental sources, as well as of individual compounds. However, only a few studies have been made on the toxicological effects of extracts derived from airborne particulate matter in chicken embryo. These studies showed that the toxic effect was due to the polycyclic aromatic hydrocarbons (PAHs) in the particles, although their structure and quantity were the factors determining the extent of the toxicity. Airborne particulate matter is composed of particles of different sizes, which can be separated into five classes according to their size by an Andersen high-volume sampler. Each class contained many kinds of compounds such as PAHs. In this study, airborne particulate matter was extracted according to particle size, the extracts analyzed for PAHs, and tested for embryotoxicity.

  1. Characteristics of wintertime polycyclic aromatic hydrocarbon assemblage in aerosol of the Southern Adriatic

    Science.gov (United States)

    Jovanović, V. Ž.; Pfendt, P. A.; Filipović, A. J.

    2007-09-01

    Features of polycyclic aromatic hydrocarbon (PAH) assemblage in aerosol samples collected from the atmosphere of Herceg Novi during the winter months of two successive years were studied. The results showed almost the same concentration profiles of identified PAHs for samples from the two periods analyzed, generally suggesting a similar origin. Diagnostic ratios indicated combustion of wood and coal, emissions from petrol and diesel engines, and dust resuspension as sources that predominantly contributed to the atmospheric PAH concentrations. Statistical analysis, principal component analysis (PCA) in particular, allowed us to identify the impact of meteorological parameters on PAH abundance.

  2. Physicochemical and Toxicological Characteristics of Semi-volatile Components of Atmospheric Aerosols in an Urban Environment

    Science.gov (United States)

    Verma, V.; Pakbin, P.; Cheung, K. L.; Cho, A. K.; Schauer, J. J.; Shafer, M. M.; Kleinman, M. T.; Sioutas, C.

    2010-12-01

    Recent toxicological studies have confirmed the oxidative properties of atmospheric aerosols and their capability to generate reactive oxygen species (ROS) in biological systems (Chen and Lippmann, 2009). While the links between aerosol toxicity and refractory transition metals present in ambient particulate matter (PM) have been documented, there are limited studies investigating the oxidative characteristics of semi-volatile species. The goal of present study is to examine the contribution of semi-volatile compounds in the oxidative potential of atmospheric aerosols. Concentrated ambient and thermodenuded quasi-ultrafine particles (dithiothreitol) assay. Detailed chemical analyses of PM samples, including organic and elemental carbon, water soluble elements, inorganic ions and polycyclic aromatic hydrocarbons (PAHs), were conducted to quantify the volatility profiles of different PM species, and also to investigate their effect on the measured oxidative potential. Refractory constituents, such as metals and elemental carbon, were marginally affected by heating, while labile species such as organic carbon and PAHs showed progressive loss in concentration with increase in TD temperature. The DTT-measured oxidative potential of PM was significantly decreased as the aerosols were heated and their semi-volatile components were progressively removed (42 %, 47 % and 66 % decrease in DTT activity at 50, 100 and 200 oC, respectively). Regression analysis performed between chemical constituents and DTT activity showed that the oxidative potential was strongly correlated with organic carbon and PAHs (R≥0.80; p≤0.05). Thus, semi-volatile organic compounds present in atmospheric aerosols constitute a substantial fraction of the PM oxidative potential, which is largely responsible for the aerosol toxicity. References: Chen, L.C., Lippmann, M., 2009. Effects of metals within ambient air particulate matter (PM) on human health. Inhalation Toxicology 21 (1), 1-31.

  3. PAH Accessibility in Particulate Matter from Road-Impacted Environments.

    Science.gov (United States)

    Allan, Ian J; O'Connell, Steven G; Meland, Sondre; Bæk, Kine; Grung, Merete; Anderson, Kim A; Ranneklev, Sissel B

    2016-08-01

    Snowmelt, surface runoff, or stormwater releases in urban environments can result in significant discharges of particulate matter-bound polycyclic aromatic hydrocarbons (PAHs) into aquatic environments. Recently, more-specific activities such as road-tunnel washing have been identified as contributing to contaminant load to surface waters. However, knowledge of PAH accessibility in particulate matter (PM) of urban origin that may ultimately be released into urban surface waters is limited. In the present study, we evaluated the accessibility of PAHs associated with seven distinct (suspended) particulate matter samples collected from different urban sources. Laboratory-based infinite sink extractions with silicone rubber (SR) as the extractor phase demonstrated a similar pattern of PAH accessibility for most PM samples. Substantially higher accessible fractions were observed for the less-hydrophobic PAHs (between 40 and 80% of total concentrations) compared with those measured for the most-hydrophobic PAHs (wash waters, first-order desorption rates for PAHs with log Kow > 5.5 were found in line with those commonly found for slowly or very slowly desorbing sediment-associated contaminants. PAHs with log Kow wash waters when surfactants are used. The implications of total and accessible PAH concentrations measured in our urban PM samples are discussed in a context of management of PAH and PM emission to the surrounding aquatic environment. Although we only fully assessed PAHs in this work, further study should consider other contaminants such as OPAHs, which were also detected in all PM samples. PMID:27312518

  4. Dihydrodiol dehydrogenase and polycyclic aromatic hydrocarbon metabolism

    Energy Technology Data Exchange (ETDEWEB)

    Smithgall, T.E.

    1986-01-01

    Carcinogenic activation of polycyclic aromatic hydrocarbons by microsomal monoxygenases proceeds through trans-dihydrodiol metabolites to diol-epoxide ultimate carcinogens. This thesis directly investigated the role of dihydrodiol dehydrogenase, a cytosolic NAD(P)-linked oxidoreductase, in the detoxification of polycyclic aromatic trans-dihydrodiols. A wide variety of non-K-region trans-dihydrodiols were synthesized and shown to be substrates for the homogeneous rat liver dehydrogenase, including several potent proximate carcinogens derived from 7,12-dimethylbenz(a)anthracene, 5-methylchrysene, and benzo(a)pyrene. Since microsomal activation of polycyclic aromatic hydrocarbons is highly stereospecific, the stereochemical course of enzymatic trans-dihydrodiol oxidation was monitored using circular dichroism spectropolarimetry. The major product formed from the dehydrogenase-catalyzed oxidation of the trans-1,2-dihydrodiol of naphthalene was characterized using UV, IR, NMR, and mass spectroscopy, and appears to be 4-hydroxy-1,2-naphthoquinone. Mass spectral analysis suggests that an analogous hydroxylated o-quinone is formed as the major product of benzo(a)pyrene-7,8-dihydrodiol oxidation. Enzymatic oxidation of trans-dihydrodiols was shown to be potently inhibited by all of the major classes of the nonsteroidal antiinflammatory drugs. Enhancement of trans-dihydrodiol proximate carcinogen oxidation may protect against possible adverse effects of the aspirin-like drugs, and help maintain the balance between activation and detoxification of polycyclic aromatic hydrocarbons.

  5. Analytical Procedure Development to Determine Polycyclic Aromatic Compounds in the PM{sub 2}.5-PM{sub 1}0 Fraction of Atmospheric Aerosols; Desarrollo de una Metodologia Analitica para la Determinacion de Compuestos Aromaticos Policiclicos en las Fracciones PM{sub 2}.5-PM{sub 1}0 del Aerosol Atmosferico

    Energy Technology Data Exchange (ETDEWEB)

    Barrado, A. I.; Garcia, S.; Perez, R. M.

    2013-06-01

    This paper presents an optimized and validated analytical methodology for the determination of various polycyclic aromatic compounds in ambient air using liquid chromatography with fluorescence detection. This analysis method was applied to samples obtained during more than one year in an area of Madrid. Selected compounds have included thirteen polycyclic hydrocarbons considered priorities by the EPA, and hydroxylated derivatives, which have been less investigated in air samples by liquid chromatography with fluorescence detection. We have characterized and compared the concentration ranges of compounds identified and studied seasonal and monthly variations. In addition, the techniques have been applied to study multivariate correlations, factor analysis and cluster analysis to extract as much information as possible for interpretation and more complete and accurate characterization of the results and their relationship with meteorological parameters and physicochemical. (Author) 50 refs.

  6. Particulate airborne impurities

    OpenAIRE

    Wilkinson, Kai

    2013-01-01

    The cumulative effects of air pollutants are of principal concern in research on environmental protection in Sweden. Post-industrial society has imposed many limits on emitted air pollutants, yet the number of reports on the negative effects from them is increasing, largely due to human activity in the form of industrial emissions and increased traffic flows. Rising concerns over the health effects from airborne particulate matter (PM) stem from in vitro, in vivo, and cohort studies revealing...

  7. ADVANCED HYBRID PARTICULATE COLLECTOR

    Energy Technology Data Exchange (ETDEWEB)

    Stanley J. Miller; Grant L. Schelkoph; Grant E. Dunham

    2000-12-01

    A new concept in particulate control, called an advanced hybrid particulate collector (AHPC), is being developed under funding from the US Department of Energy. The AHPC combines the best features of electrostatic precipitators (ESPs) and baghouses in an entirely novel manner. The AHPC concept combines fabric filtration and electrostatic precipitation in the same housing, providing major synergism between the two methods, both in the particulate collection step and in transfer of dust to the hopper. The AHPC provides ultrahigh collection efficiency, overcoming the problem of excessive fine-particle emissions with conventional ESPs, and solves the problem of reentrainment and recollection of dust in conventional baghouses. Phase I of the development effort consisted of design, construction, and testing of a 5.7-m{sup 3}/min (200-acfm) working AHPC model. Results from both 8-hour parametric tests and 100-hour proof-of-concept tests with two different coals demonstrated excellent operability and greater than 99.99% fine-particle collection efficiency.

  8. Atmospheric emissions as a tool in evaluation of sustainability research in oil industry; Emissao atmosferica como uma ferramenta na avaliacao do desenvolvimento sustentavel na industria do petroleo

    Energy Technology Data Exchange (ETDEWEB)

    Zanella, Nicolas P.; Baich, Paulo R.M.; Machado, Maria I. [Fundacao Universidade do Rio Grande (FURG), RS (Brazil)

    2008-07-01

    This work is directly to analysis of atmosphere surrounding Ipiranga Refinery; witch is located in the city of Rio Grande, in estate of Rio Grande do Sul. The refinery is surrounded by neighborhood, witch are impacted by atmospheric emissions of refinery. The objective of this work is correlating the refinery to the inhabitants that lives near the refinery, using an environmental sustainability index. This work will be achieve by analysis of Polycyclic Aromatic Hydrocarbons (PAH) bounded in particulate matter with diameter of 100 {mu}m (PTS), the acquisition of health data on the city hospitals and correlation of this data with PAH concentrations in Particulate Matter. The Samples were obtain by FEPAM, witch have three samples sites in the center of city. The samples was obtained by a High Volume Sampler equipped with quartz fiber filters. The meteorological data important to this work, like wind direction and speed, will be obtain in Meteorological Station on FURG. The results expect to this work are the quantification of PAH bounded with PM-100 and the quantification of PAH emitted by Ipiranga Refinery. And possibly, to correlate this data to made the Environmental Sustainability index. (author)

  9. Characterization of aromaticity in analogues of titan's atmospheric aerosols with two-step laser desorption ionization mass spectrometry

    OpenAIRE

    Mahjoub, Ahmed; Schwell, Martin; Carrasco, Nathalie; Benilan, Yves; Cernogora, Guy; Szopa, Cyril; Gazeau, Marie-Claire

    2016-01-01

    The role of polycyclic aromatic hydrocarbons (PAH) and Nitrogen containing PAH (PANH) as intermediates of aerosol production in the atmosphere of Titan has been a subject of controversy for a long time. An analysis of the atmospheric emission band observed by the Visible and Infrared Mapping Spectrometer (VIMS) at 3.28 micrometer suggests the presence of neutral polycyclic aromatic species in the upper atmosphere of Titan. These molecules are seen as the counter part of negative and positive ...

  10. Particulate matter formation from photochemical degradation of organophosphorus pesticides

    Science.gov (United States)

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

    2015-12-01

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

  11. VIIRSN Level-3 Standard Mapped Image, Particulate Organic Carbon, Monthly, 4km

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — NOAA CoastWatch distributes Particulate Organic Carbon data from ther NPP-Suomi spacecraft. Measurements are gathered by VIIRS instrument carried aboard the...

  12. 40 CFR 60.132 - Standard for particulate matter.

    Science.gov (United States)

    2010-07-01

    ... reverberatory furnace any gases which: (1) Contain particulate matter in excess of 50 mg/dscm (0.022 gr/dscf... subpart shall discharge or cause the discharge into the atmosphere from any blast (cupola) or electric furnace any gases which exhibit 10 percent opacity or greater....

  13. Polycyclic aromatic compounds in shale oils: influence of process conditions

    Energy Technology Data Exchange (ETDEWEB)

    Williams, P.T.; Nazzal, J.M. [University of Leeds (United Kingdom). Dept. of Fuel and Energy

    1998-08-01

    Polycyclic aromatic compounds (PAC) are a significant environmental chemical group, with an associated health hazard. They have been shown to be present in oils derived from the pyrolysis of oil shales; however, the influence of process conditions on their concentration is less well known. Oil shales were pyrolysed in a 200 cm{sup 3} stainless steel fixed bed reactor in relation to temperature from 400{sup o}C to 620{sup o}C in both a nitrogen and nitrogen/steam atmosphere. The condensed oils were analysed for their content of PAC, including polycyclic aromatic hydrocarbons (PAH), sulphur-PAH (PASH) and Nitrogen-PAH (PANH). The derived gases were analysed in terms of H{sub 2}, CO, CO{sub 2}, CH{sub 4} and other hydrocarbons to C{sub 4} and the alkene/alkane ratio determined. The derived shale oils were found to contain significant concentrations of PAH, PASH and PANH some of which have been shown to be biologically active. The main PAH were napthalene, fluorene and phenanthrene and their alkylated homologues; PASH identified included, benzothiophene, and dibenzothiophene and the PANH included indole, carbazole and quinoline and their alkylated derivatives. The concentration of PAC increased with increasing pyrolysis temperature and their formation was linked to increased secondary reactions as indicated by the gas phase alkene/alkane ratio. The influence of steam was to increase the yield of oil significantly. The presence of steam also increased the concentration of PAC in the derived shale oil compared to using nitrogen as the sweep gas. (author)

  14. Airborne Particulate Threat Assessment

    Energy Technology Data Exchange (ETDEWEB)

    Patrick Treado; Oksana Klueva; Jeffrey Beckstead

    2008-12-31

    Aerosol threat detection requires the ability to discern between threat agents and ambient background particulate matter (PM) encountered in the environment. To date, Raman imaging technology has been demonstrated as an effective strategy for the assessment of threat agents in the presence of specific, complex backgrounds. Expanding our understanding of the composition of ambient particulate matter background will improve the overall performance of Raman Chemical Imaging (RCI) detection strategies for the autonomous detection of airborne chemical and biological hazards. Improving RCI detection performance is strategic due to its potential to become a widely exploited detection approach by several U.S. government agencies. To improve the understanding of the ambient PM background with subsequent improvement in Raman threat detection capability, ChemImage undertook the Airborne Particulate Threat Assessment (APTA) Project in 2005-2008 through a collaborative effort with the National Energy Technology Laboratory (NETL), under cooperative agreement number DE-FC26-05NT42594. During Phase 1 of the program, a novel PM classification based on molecular composition was developed based on a comprehensive review of the scientific literature. In addition, testing protocols were developed for ambient PM characterization. A signature database was developed based on a variety of microanalytical techniques, including scanning electron microscopy, FT-IR microspectroscopy, optical microscopy, fluorescence and Raman chemical imaging techniques. An automated particle integrated collector and detector (APICD) prototype was developed for automated collection, deposition and detection of biothreat agents in background PM. During Phase 2 of the program, ChemImage continued to refine the understanding of ambient background composition. Additionally, ChemImage enhanced the APICD to provide improved autonomy, sensitivity and specificity. Deliverables included a Final Report detailing our

  15. Particulate contamination in ampoules.

    Science.gov (United States)

    Alexander, D M; Veltman, A M

    1985-01-01

    The particulate contamination in 19 formulations of solutions in ampoules supplied by eight South African manufacturers, thirty-three batches in all, was analysed using a HIAC PC 320 light blockage particle analyser linked to a CMB 60 sensor. Results showed that the level of contamination was generally low and that, where comparisons could be made, manufacturers both of the ampoules and the solutions maintained similarly high standards. Problems in this field appeared to be related to the formulation or the quality of the raw material. PMID:2858528

  16. Polycyclic aromatic hydrocarbon formation under simulated coal seam pyrolysis conditions

    Institute of Scientific and Technical Information of China (English)

    Liu Shuqin; Wang Yuanyuan; Wang Caihong; Bao Pengcheng; Dang Jinli

    2011-01-01

    Coal seam pyrolysis occurs during coal seam fires and during underground coal gasification.This is an important source of polycyclic aromatic hydrocarbon (PAH) emission in China.Pyrolysis in a coal seam was simulated in a tubular furnace.The 16 US Environmental Protection Agency priority controlled PAHs were analyzed by HPLC.The effects of temperature,heating rate,pyrolysis atmosphere,and coal size were investigated.The results indicate that the 3-ring PAHs AcP and AcPy are the main species in the pyrolysis gas.The 2-ring NaP and the 4-ring Pyr are also of concern.Increasing temperature caused the total PAH yield to go through a minimum.The lowest value was obtained at the temperature of 600 ℃ Higher heating rates promote PAH formation,especially formation of the lower molecular weight PAHs.The typical heating rate in a coal seam,5 ℃/min,results in intermediate yields of PAHs.The total PAHs yield in an atmosphere of N2 is about 1.81 times that seen without added N2,which indicates that an air flow through the coal seam accelerates the formation of PAHs.An increase in coal particle size reduces the total PAHs emission but promotes the formation of 5- and 6-ring PAHs.

  17. Estimation of particulate matter from simulation and measurements

    Science.gov (United States)

    Nakata, Makiko; Nakano, Tomio; Okuhara, Takaaki; Sano, Itaru; Mukai, Sonoyo

    2011-11-01

    The particulate matter is a typical indicator of small particles in the atmosphere. In addition to providing impacts on climate and environment, these small particles can bring adverse effects on human health. Then an accurate estimation of particulate matter is an urgent subject. We set up SPM sampler attached to our AERONET (Aerosol Robotics Network) station in urban city of Higashi-Osaka in Japan. The SPM sampler provides particle information about the concentrations of various SPMs (e.g., PM10 and PM2.5) separately. The AEROENT program is world wide ground based sunphotometric observation networks by NASA and provides the spectral information about aerosol optical thickness (AOT) and Angstrom exponent (α). Simultaneous measurements show that a linear correlation definitely exists between AOT and PM2.5. These results indicate that particulate matter can be estimated from AOT. However AOT represents integrated values of column aerosol amount retrieved from optical property, while particulate matter concentration presents in-situ aerosol loading on the surface. Then simple way using linear correlation brings the discrepancy between observed and estimated particulate matter. In this work, we use cluster information about aerosol type to reduce the discrepancy. Our improved method will be useful for retrieving particulate matter from satellite measurements.

  18. Spectroscopic Characterisation of Novel Polycyclic Aromatic Polymers

    OpenAIRE

    O'Neill, Luke; Lynch, Patrick; McNamara, Mary; Byrne, Hugh

    2007-01-01

    A series of novel polyphenylenevinylene (PPV) derivative polymers were studied by absorption and photoluminescence spectroscopies. The effect of the sequential introduction of polycyclic aromatic ring substituents into the delocalized backbone was examined with relation to hypsochromatic and bathochromatic shifting. While the replacement of the phenyl units by naphthyl units results in a substantial hypsochromic shift of both the absorption and emission spectra, their subsequent substitution ...

  19. Atmospheric transformation of diesel emissions.

    Science.gov (United States)

    Zielinska, Barbara; Samy, Shar; McDonald, Jacob D; Seagrave, JeanClare

    2010-04-01

    The hypothesis of this study was that exposing diesel exhaust (DE*) to the atmosphere transforms its composition and toxicity. Our specific aims were (1) to characterize the gas- and particle-phase products of atmospheric transformations of DE under the influence of daylight, ozone (O3), hydroxyl (OH) radicals, and nitrate (NO3) radicals; and (2) to explore the biologic activity of DE before and after the transformations took place. The study was executed with the aid of the EUPHORE (European Photoreactor) outdoor simulation chamber facility in Valencia, Spain. EUPHORE is one of the largest and best-equipped facilities of its kind in the world, allowing investigation of atmospheric transformation processes under realistic ambient conditions (with dilutions in the range of 1:300). DE was generated on-site using a modern light-duty diesel engine and a dynamometer system equipped with a continuous emission-gas analyzer. The engine (a turbocharged, intercooled model with common-rail direct injection) was obtained from the Ford Motor Company. A first series of experiments was carried out in January 2005 (the winter 2005 campaign), a second in May 2005 (the summer 2005 campaign), and a third in May and June 2006 (the summer 2006 campaign). The diesel fuel that was used closely matched the one currently in use in most of the United States (containing 47 ppm sulfur and 15% aromatic compounds). Our experiments examined the effects on the composition of DE aged in the dark with added NO3 radicals and of DE aged in daylight with added OH radicals both with and without added volatile organic compounds (VOCs). In order to remove excess nitrogen oxides (NO(x)), a NO(x) denuder was devised and used to conduct experiments in realistic low-NO(x) conditions in both summer campaigns. A scanning mobility particle sizer was used to determine the particle size and the number and volume concentrations of particulate matter (PM) in the DE. O3, NO(x), and reactive nitrogen oxides (NO

  20. Emissions of polycyclic aromatic hydrocarbons from coking industries in China

    Institute of Scientific and Technical Information of China (English)

    Ling Mu; Lin Peng; Junji Cao; Qiusheng He; Fan Li; Jianqiang Zhang; Xiaofeng Liu

    2013-01-01

    This study set out to assess the characteristics of polycyclic aromatic hydrocarbon (PAH) emission from coking industries,with field samplings conducted at four typical coke plants.For each selected plant,stack flue gas samples were collected during processes that included charging coal into the ovens (CC),pushing coke (PC) and the combustion of coke-oven gas (CG).Sixteen individual PAHs on the US EPA priority list were analyzed by gas chromatography/mass spectrometry (GC/MS).Results showed that the total PAH concentrations in the flue gas ranged from 45.776 to 414.874 μg/m3,with the highest emission level for CC (359.545 μg/m3).The concentration of PAH emitted from the CC process in CP1 (stamp charging) was lower than that from CP3 and CP4 (top charging).Low-molecular-weight PAHs (i.e.,two-to three-ring PAHs) were predominant contributors to the total PAH contents,and Nap,AcPy,Flu,PhA,and AnT were found to be the most abundant ones.Total BaPeq concentrations for CC (2.248 iμg/m3) were higher than those for PC (1.838 μg/m3) and CG (1.082 μg/m3),and DbA was an important contributor to carcinogenic risk as BaP in emissions from coking processes.Particulate PAH accounted for more than 20% of the total BaPeq concentrations,which were significantly higher than the corresponding contributions to the total PAH mass concentration (5%).Both particulate and gaseous PAH should be taken into consideration when the potential toxicity risk of PAH pollution during coking processes is assessed.The mean total-PAH emission factors were 346.132 and 93.173 μg/kg for CC and PC,respectively.

  1. MEMANFAATKAN TANAMAN UNTUK MENGURANGI POLUSI PARTICULATE MATTER KE DALAM BANGUNAN

    Directory of Open Access Journals (Sweden)

    Christina E. Mediastika

    2002-01-01

    Full Text Available Inhabitants of a building are difficult to escape particulate matter emission. Within this condition, buildings should have vertical element that could block the dispersion of particulate matter to living spaces. Vegetation, a part of vertical elemen for fencing, is considered to do this task. The use of vegetation is chosen with reference to nature and behaviour of particulate matter. Earlier research found that dispersion of particulate matter is mostly at lower atmospheric layer and that particulate matter could be deposited. Therefore, low growing vegetation or climbing plants with particular leaf condition to encourage deposition is predicted suitable. Four vegetation was examined: Duranta repens, Polyscias fruticosa, Stephanotis floribunda and Scindapsus sp. As a preliminary study, there is no valid conclusion could be made from this experiment. However, there are indications that Duranta repens and Stephanotis floribunda block and deposit slightly more particulate matter than the two others. Abstract in Bahasa Indonesia : Polusi particulate matter atau partikel halus tidak hanya terjadi di jalan raya, tetapi juga masuk ke dalam bangunan yang terletak di sepanjang jalan. Oleh karenanya, bangunan seyogyanya memiliki elemen vertikal yang mampu bertugas menghalangi masuknya polusi partikel halus. Salah satu kemungkinan penggunaan elemen vertikal, yaitu tanaman yang ditempatkan pada posisi pagar diteliti dalam studi ini. Mempelajari bahwa partikel halus dengan ukuran tertentu dapat diendapkan dan penyebarannya umumnya terjadi pada lapisan udara rendah, maka studi terhadap tanaman semak atau perdu atau tanaman rambat dengan jenis permukaan daun tertentu lebih diutamakan. Empat jenis tanaman diuji kemampuannya, yaitu: Duranta repens, Polyscias fruticosa, Stephanotis floribunda and Scindapsus sp. Sebagai studi yang sangat awal, masih belum ada hasil valid yang ditawarkan, namun setidaknya ditemukan indikasi bahwa Duranta repens and Stephanotis

  2. Depletion of gaseous polycyclic aromatic hydrocarbons by a forest canopy

    Directory of Open Access Journals (Sweden)

    S.-D. Choi

    2008-07-01

    Full Text Available Rapid uptake of gaseous polycyclic aromatic hydrocarbons (PAHs by a forest canopy was observed at Borden in Southern Ontario, Canada during bud break in early spring 2003. High volume air samples were taken on 12 individual days at three different heights (44.4, 29.1, and 16.7 m on a scaffolding tower and on the forest floor below the canopy (1.5 m. Concentrations of PAHs were positively correlated to ambient temperature, resulting from relatively warm and polluted air masses passing over the Eastern United States and Toronto prior to arriving at the sampling site. An analysis of vertical profiles and gas/particle partitioning of the PAHs showed that gaseous PAHs established a concentration gradient with height, whereas levels of particulate PAHs were relatively uniform, implying that only the uptake of gaseous PAHs by the forest canopy was sufficiently rapid to be observed. Specifically, the gaseous concentrations of intermediate PAHs, such as phenanthrene, anthracene, and pyrene, during budburst and leaf emergence were reduced within and above the canopy. When a gradient was observed, the percentage of PAHs on particles increased at the elevations experiencing a decrease in gas phase concentrations. The uptake of intermediate PAHs by the canopy also led to significant differences in gaseous PAH composition with height. These results are the most direct evidence yet of the filter effect of forest canopies for gaseous PAHs in early spring. PAH deposition fluxes and dry gaseous deposition velocities to the forest canopy were estimated from the concentration gradients.

  3. Dry deposition of polycyclic aromatic hydrocarbons in ambient air

    International Nuclear Information System (INIS)

    Dry deposition and air sampling were undertaken, simultaneously, in the ambient air of an urban site and a petrochemical-industry (PCI) plant by using several dry deposition plates and PS-1 samplers from January to May 1994 in southern Taiwan. The dry deposition plate with a smooth surface was always pointed into the wind. Twenty-one polycyclic aromatic hydrocarbons (PAHs) were analyzed by a gas chromatography/mass spectrometer (GC/MSD). The dry deposition flux of total-PAHs in urban and PCI sites averaged 166 and 211 microg/m2·d, respectively. In general, the PAH dry deposition flux increased with increases in the PAH concentration in the ambient air. The PAH pattern of dry deposition flux in both urban and PCI sites were similar to the pattern measured by the filter of the PS-1 sampler and completely different from the PAH pattern in the gas phase. The higher molecular weight PAHs have higher dry deposition velocities. This is due to the fact that higher molecular weight PAHs primarily associated with the particle phase are deposited mostly by gravitational settling, while the gas phase PAHs were between 0.001 and 0.010 cm/s, only the lower molecular-weight PAHs--Nap and AcPy--had a significant fraction of dry deposition flux contributed by the gas phase. All the remaining higher molecular-weight PAHs had more than 94.5% of their dry deposition flux resulting from the particle phase. This is due to the fact that higher molecular weight PAHs have a greater fraction in the particle phase and the dry deposition velocities of particulates are much higher than those of the gas phase

  4. 'Mussel Watch' and chemical contamination of the coasts by polycyclic aromatic hydrocarbons

    International Nuclear Information System (INIS)

    Polycyclic aromatic hydrocarbons (PAH) enter the coastal marine environment from three general categories of sources; pyrogenic, petrogenic (or petroleum), and natural diagenesis. PAH from different sources appear to have differential biological availability related to how the PAH are sorbed, trapped, or chemically bound to particulate matter, including soot. Experience to date with bivalve sentinel organism, or 'Mussel Watch', monitoring programs indicates that these programs can provide a reasonable general assessment of the status and trends of biologically available PAH in coastal ecosystems. As fossil fuel use increases in developing countries, it is important that programs such as the International Mussel Watch Program provide assessments of the status and trends of PAH contamination of coastal ecosystems of these countries. (author)

  5. Simultaneously catalytic removal of NOx and particulate matter on diesel particulate filter

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The simultaneous removal of NOx and particulate matter (PM) exhausted from diesel engine was studied with a diesel particulate filter (DPF) on which a mixed metal oxide catalyst, Cu0.95K0.05Fe2O4 was loaded. The NOx reduction was observed in the same temperature range of the CO2 formation, implying the occurrence of the simultaneous removal of NOx and PM in an oxidizing atmosphere. It was shown that SOF and soot in PM are attributed to the reduction of NOx at lower and higher temperatures, respectively. The oxidation of PM was enhanced by the coexistence of NO and O2. The ignition and exhaustion temperatures of PM decrease as the order NO>O2>NO+O2. This is a combined process of PM trapping as well as the catalytic reactions of soot oxidation and NOx reduction, promising the most desirable after-treatment of diesel exhausts.

  6. The effect of microscopic charged particulates in space weather

    Energy Technology Data Exchange (ETDEWEB)

    Popel, S I; Kopnin, S I [Institute for Dynamics of Geospheres RAS, Leninsky pr. 38, bld. 1, 119334 Moscow (Russian Federation); Yu, M Y [Institute for Fusion Theory and Simulation, Zhejiang University, Hangzhou 310027 (China); Ma, J X [CAS Key Laboratory of Basic Plasma Physics and Department of Modern Physics, University of Science and Technology of China, Hefei, Anhui 230026 (China); Huang Feng, E-mail: s_i_popel@mtu-net.ru, E-mail: popel@idg.chph.ras.ru [College of Science, China Agricultural University, Beijing 100083 (China)

    2011-05-04

    Space weather is a relatively new and important field of research. It is relevant to diverse topics such as radio communication, space travel, diagnostics of ionospheric and space plasmas, detection of pollutants and re-entry objects, prediction of terrestrial weather and global warming. Recently it has been shown that nano- and micrometre-sized electrically charged particulates from interplanetary space and from the Earth's atmosphere can affect the local properties as well as the diagnostics of the interplanetary, magnetospheric, ionospheric and terrestrial complex plasmas. In this report the sources of the charged dust particulates and the effects of the latter on the near-Earth space weather are examined.

  7. The effect of microscopic charged particulates in space weather

    International Nuclear Information System (INIS)

    Space weather is a relatively new and important field of research. It is relevant to diverse topics such as radio communication, space travel, diagnostics of ionospheric and space plasmas, detection of pollutants and re-entry objects, prediction of terrestrial weather and global warming. Recently it has been shown that nano- and micrometre-sized electrically charged particulates from interplanetary space and from the Earth's atmosphere can affect the local properties as well as the diagnostics of the interplanetary, magnetospheric, ionospheric and terrestrial complex plasmas. In this report the sources of the charged dust particulates and the effects of the latter on the near-Earth space weather are examined.

  8. Emission factors for carbonaceous particles and polycyclic aromatic hydrocarbons from residential coal combustion in China.

    Science.gov (United States)

    Chen, Yingjun; Sheng, Guoying; Bi, Xinhui; Feng, Yanli; Mai, Bixian; Fu, Jiamo

    2005-03-15

    Emission factors of carbonaceous particles, including black carbon (BC) and organic carbon (OC), and polycyclic aromatic hydrocarbons (PAHs) were determined for five coals, which ranged in maturity from sub-bituminous to anthracite. They were burned in the form of honeycomb briquettes in a residential coalstove, one of the most common fuel/stove combinations in China. Smoke samples were taken through dilution sampling equipment, with a high volume sampler that could simultaneously collect emissions in both particulate and gaseous phases, and a cascade impactor that could segregate particles into six fractions. Particulate BC and OC were analyzed by a thermal-optical method, and PAHs in emissions of both phases were analyzed by GC-MS. Burning of bituminous coals produced the highest emission factors of particulate matter (12.91 g/kg), BC (0.28 g/kg), OC (7.82 g/kg), and 20 PAHs (210.6 mg/kg) on the basis of burned dry ash-free (daf) coal, while the anthracite honeycomb-briquette was the cleanest household coal fuel. The size-segregated results show that more than 94% of the particles were submicron, and calculated mass median aerodynamic diameters (MMAD) of all particles were under 0.3 microm. Based on the coal consumption in the residential sector of China, 290.24 Gg (gigagrams) of particulate matter, 5.36 Gg of BC, 170.33 Gg of OC, and 4.72 Gg of 20 PAHs mass were emitted annually from household honeycomb-briquette burning during 2000. Anthracite coal should be selected preferentially and more advanced burning conditions should be applied in domestic combustion, from the viewpoint of both climate change and adverse health effects. PMID:15819248

  9. Soil sealing degree as factor influencing urban soil contamination with polycyclic aromatic hydrocarbons (PAHs

    Directory of Open Access Journals (Sweden)

    Mendyk Łukasz

    2016-03-01

    Full Text Available The objective of the study was to determine role of soil sealing degree as the factor influencing soil contamination with polycyclic aromatic hydrocarbons (PAHs. The study area included four sampling sites located within the administrative boundaries of the Toruń city, Poland. Sampling procedure involved preparing soil pits representing three examples of soil sealing at each site: non-sealed soil as a control one (I and two degrees of soil sealing: semi-pervious surface (II and totally impervious surface (III. Together with basic properties defined with standard procedures (particle size distribution, pH, LOI, content of carbonates content of selected PAHs was determined by dichloromethane extraction using gas chromatography with mass spectrometric detection (GC-MS. Obtained results show that urban soils in the city of Toruń are contaminated with polycyclic aromatic hydrocarbons. Soil sealing degree has a strong influence on the soil contamination with polycyclic aromatic hydrocarbons. Totally sealed soils are better preserved from atmospheric pollution including PAHs. Combustion of grass/wood/coal was the main source of determined PAHs content in examined soils.

  10. Comparison of the Concentration Profiles of 12 Polycyclic Aromatic Hydrocarbons from Different Sources with Monitoring Data from Prague Using a Similarity Measure

    Czech Academy of Sciences Publication Activity Database

    Tydlitát, Vratislav; Kotlík, B.; Punčochář, Miroslav; Mikešová, M.

    2010-01-01

    Roč. 30, č. 4 (2010), s. 208-221. ISSN 1040-6638 Institutional research plan: CEZ:AV0Z40720504 Keywords : car exhausts * polycyclic aromatic hydrocarbons (PAHs) * urban atmosphere Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 0.982, year: 2010

  11. Quantitative elemental determination of the particulate matter in the atmosphere of Pachuca city and the Real del Monte village, Hidalgo by means of PIXE technique; Determinacion elemental cuantitativa de la materia particulada en la atmosfera de la ciudad de Pachuca y el poblado de Real del Monte, Hidalgo, mediante la tecnica PIXE

    Energy Technology Data Exchange (ETDEWEB)

    Guasso G, C.L. [ITT, 50000 Toluca (Mexico)

    2001-07-01

    All the pollutants that are generated so much of anthropogenic activities as natural cause effects to the health, and of course its increase the atmospheric pollution. Today in day for the great advance of the technology other pollutants are even generated but noxious to the human being's health, such it is the case of the particles, which are also called particulate matter airborne (MPA). This has motivated, to establish control measures leaning in collection strategies and certified analysis techniques, accurate and reliable. In the National Institute of Nuclear Research (ININ) they have been carried out studies on particulate matter airborne. In 1991 it was installed, calibrated and validated the nuclear technique of atomic origin based on proton beams known as PIXE. The characterization of the (MPA) it is carried out applying this technique and the collection by means of Dichotomous collectors (SFU). The thesis work that is presented next, includes the topic of the atmospheric pollution by particulate matter airborne (MPA) in a mining region, inside the Hidalgo State. The study was carried out during the 1998 winter season, only embracing the whole month of March in alternate days giving a total of 112 samples. Two sites that are highly active in the mining were studied, these are: the Real del Monte town and the Hidalgo state capital: Pachuca. Four samples per day were collected beginning to the 7:00 am--7:00 pm (daytime period) and concluding to the 7:00 pm -7:00 am (nocturne period). The characterization of its elementary content is carried out using the X-ray emission induced by particles technique (PIXE) that is a nuclear technique able to analyze 23 chemical elements beginning from the Al to the Pb, it requires of a very small sample quantity, it is very sensitive and it is not destructive. This characterization one carries out so much for fraction PM{sub 2.5} (fine) like as PM{sub 10} (thick) in both sites, also it was analyzed the temporary

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

    International Nuclear Information System (INIS)

    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)

  13. Composition of airborne particulate matter in the industrial area versus mountain area

    Directory of Open Access Journals (Sweden)

    Barbora Sýkorová

    2016-03-01

    Full Text Available The paper deals with research of air pollution in two different locations on the Moravian-Silesian Region, Czech Republic. These are the sites Ostrava-Radvanice, which is located in the area affected by the industry and Ostravice in the mountains (without significant effect of the industry. The dust particles collected at these locations were subjected to a wide range of analyses. The mass concentration, the mass-size distribution, mineralogical composition, the concentration of PAHs (polycyclic aromatic hydrocarbons, and the concentrations of selected metals (Cd, Pb, Zn, Fe, Mn, As, Ni, Co, and Cr were observed at the particulate matter.

  14. Carcinogenicity of airborne fine particulate benzo(a)pyrene: an appraisal of the evidence and the need for control.

    OpenAIRE

    PERERA, F.

    1981-01-01

    Benzo(a)pyrene(BaP) originating from fossil fuel and other organic combustion processes is largely adsorbed on fine particulate and hence is a widespread atmospheric pollutant. Available emissions and air quality data are based on the total weight of particulate matter without reference to size and give little information on trends and concentrations of fine particulate BaP. Greater reliance on coal, synfuels and diesel fuel for energy production and transportation will significantly increase...

  15. Identifying and dating buried micropodzols in Subatlantic polycyclic drift sands

    NARCIS (Netherlands)

    J. Wallinga; J.M. van Mourik; M.L.M. Schilder

    2013-01-01

    Polycyclic soil sequences provide valuable archives of alternating unstable periods (sand drifting) and stable periods (soil formation) in NW-European coversand landscapes during the Subatlantic. Here we study six polycyclic soil sequences at the Weerterbergen (The Netherlands) to investigate how to

  16. Microdosimetry of internal, particulate sources

    International Nuclear Information System (INIS)

    The theory of microdosimetry is extended to include particulate and non-uniformly distributed sources typical of internally deposited radioisotopes. An example is presented in which stationary particulates of 239Pu of negligible physical size are distributed at random in a tissue in which the sensitive sites are also assumed to be randomly distributed. Preliminary calculations are reported for this model of the probability density in specific energy of all the sites and of the fraction of sites in which no energy is deposited for particulates that emit between 1 and 100,000 alpha particles

  17. The chemistry of the polycyclic polyprenylated acylphloroglucinols.

    Science.gov (United States)

    Richard, Jean-Alexandre; Pouwer, Rebecca H; Chen, David Y-K

    2012-05-01

    With their fascinating biological profiles and stunningly complex molecular architectures, the polycyclic polyprenylated acylphloroglucinols (PPAPs) have long provided a fertile playing field for synthetic organic chemists. In particular, the recent advent of innovative synthetic methods and strategies together with C-C bond-forming reactions and asymmetric catalysis have revitalized this field tremendously. Consequently, PPAP targets which once seemed beyond reach have now been synthesized. This Review aims to highlight the recent achievements in the total synthesis of PPAPs, as well as notable methods developed for the construction of the bicyclo[3.3.1] core of these chemically and biologically intriguing molecules. PMID:22461155

  18. Cytotoxic polycyclic polyprenylated acylphloroglucinols from Hypericum attenuatum.

    Science.gov (United States)

    Zhou, Zhong-bo; Zhang, Yang-mei; Pan, Ke; Luo, Jian-guang; Kong, Ling-yi

    2014-06-01

    Six new polycyclic polyprenylated acylphloroglucinols, attenuatumiones A-F (1-6), together with twelve known analogs (7-18) were isolated from the whole plant of Hypericum attenuatum. Their structures were elucidated by spectroscopic methods, and the absolute configuration of C-13 in attenuatumione C (3) was deduced via the circular dichroism datum of the in situ formed [Rh2(OCOCF3)4] complexes. All isolates were evaluated for the cytotoxic activities on three human cancer cell lines. Compound 3 showed moderate cytotoxic activities with IC50 values of 10.12 and 10.56 μM against SMMC7721 and U2OS, respectively. PMID:24603092

  19. ADVANCED HYBRID PARTICULATE COLLECTOR

    Energy Technology Data Exchange (ETDEWEB)

    Ye Zhuang; Stanley J. Miller; Michelle R. Olderbak; Rich Gebert

    2001-12-01

    A new concept in particulate control, called an advanced hybrid particulate collector (AHPC), is being developed under funding from the U.S. Department of Energy. The AHPC combines the best features of electrostatic precipitators (ESPs) and baghouses in an entirely novel manner. The AHPC concept combines fabric filtration and electrostatic precipitation in the same housing, providing major synergism between the two methods, both in the particulate collection step and in transfer of dust to the hopper. The AHPC provides ultrahigh collection efficiency, overcoming the problem of excessive fine-particle emissions with conventional ESPs, and solves the problem of reentrainment and re-collection of dust in conventional baghouses. Phase I of the development effort consisted of design, construction, and testing of a 5.7-m{sup 3}/min (200-acfm) working AHPC model. Results from both 8-hr parametric tests and 100-hr proof-of-concept tests with two different coals demonstrated excellent operability and greater than 99.99% fine-particle collection efficiency. Since all of the developmental goals of Phase I were met, the approach was scaled up in Phase II to a size of 255 m{sup 3}/min (9000 acfm) (equivalent in size to 2.5 MW) and was installed on a slipstream at the Big Stone Power Plant. For Phase II, the AHPC at Big Stone Power Plant was operated continuously from late July 1999 until mid-December 1999. The Phase II results were highly successful in that ultrahigh particle collection efficiency was achieved, pressure drop was well controlled, and system operability was excellent. For Phase III, the AHPC was modified into a more compact configuration, and components were installed that were closer to what would be used in a full-scale commercial design. The modified AHPC was operated from April to July 2000. While operational results were acceptable during this time, inspection of bags in the summer of 2000 revealed some membrane damage to the fabric that appeared to be

  20. Scavenging of particulate elemental carbon into stratus cloud

    Energy Technology Data Exchange (ETDEWEB)

    Kaneyasu, Naoki; Maeda, Takahisa [National Inst. for Resources and Environment, Tsukuba (Japan)

    1995-12-31

    The role of atmospheric aerosols on the alternation of cloud radiative properties has widely been recognized since 1977 when Tomey and his coworkers have numerically demonstrated the effect of increased cloud condensation nuclei (CCN). At the same time, cloud processes are one of the most important factor in controlling the residence time of atmospheric aerosols through the wet removal process. The redistribution of the size and the composition of pre-cloud aerosols is also the important role of cloud process on the nature of atmospheric aerosols. In order to study these cloud-aerosol interaction phenomena, the incorporation of aerosols into cloud droplets is the first mechanism to be investigated. Among the several mechanisms for the incorporation of aerosols into cloud droplets, nucleation scavenging, is the potentially important process in the view of cloud-aerosol interactions. This critical supersaturation for a given radius of a particle can be theoretically calculated only for pure species, e.g., NaCl. However, a significant portion of the atmospheric aerosols is in the form of internal mixture of multiple components, such as SO{sub 4}{sup 2-}, NO{sub 3}{sup -}, NH{sub 4}{sup +} and particulate elemental carbon. The knowledge acquired by field measurements is therefore essential on this subject. The present study focuses on the scavenging of major components of urban atmospheric aerosols, in particular the incorporation of particulate elemental carbon into stratus cloud. Particulate elemental carbon is the strongest light absorbing species in visible region, and has potential to change the optical property of cloud. On the basis of the measurements conducted at a mountain located in the suburb of Tokyo Metropolitan area, Japan, some insights on the scavenging of particulate elemental carbon into cloud droplet will be presented

  1. Characterization and source apportionment of polycyclic aromatic hydrocarbons (PAHs) in Sediments from the Bohai Sea, China

    Science.gov (United States)

    Liu, Jihua; Hu, Ningjing; Shi, Xuefa

    2015-04-01

    -related pollution were 39, 38 and 23%, respectively. Pyrogenic sources (coal combustion and traffic-related pollution) contributed 61% of anthropogenic PAHs to sediments, which indicates that energy consumption is a predominant factor in PAH pollution in the Bohai Sea. Acknowledgements: This work was jointly supported by National Science Fund, China (Grant No.40806025), the State Oceanic Administration, China (Grant No. 201105003, 908-02-02-05, and GY02-2009G19). References Fang MD, Chang WK, Lee CL, Liu JT (2009) The use of polycyclic aromatic hydrocarbons as a particulate tracer in the water column Kaoping submarine canyon. J Mar Syst 76: 457-467.

  2. Uptake of polycyclic aromatic hydrocarbons by maize plants

    International Nuclear Information System (INIS)

    Roots and above-ground parts (tops) of maize plants, comprising cuticles, leaves and stems, have been exposed separately to polycyclic aromatic hydrocarbons (PAHs) by means of air-tight bicameral exposure devices. Maize roots and tops of plants directly accumulate PAHs from aqueous solutions and from air in proportion to exposure levels. Root and leaf concentration factors (log RCF and log LCF) are log-linear functions of log-based octanol-water partition coefficient (log Kow) and log-based octanol-air partition coefficient (log Koa). The PAHs' concentrations among cuticles, leaves and stems display good correlations with each other. PAH concentrations in each part of the plant tested correlated positively with atmospheric PAHs' concentrations. Comparisons between PAHs' concentrations of root epidermis and root tissue showed similar correlations. Bulk concentrations of contaminants in various plant tissues differed greatly, but these differences disappeared after normalization to lipid contents suggesting lipid-based partitioning of PAHs among maize tissues. - PAHs can enter maize plants directly from both air and soil environment

  3. Investigation of polycyclic aromatic hydrocarbons from coal gasification

    Institute of Scientific and Technical Information of China (English)

    ZHOU Hong-cang; JIN Bao-sheng; ZHONG Zhao-ping; HUANG Ya-ji; XIAO Rui; LI Da-ji

    2005-01-01

    The hazardous organic pollutants generated from coal gasification, such as polycyclic aromatic hydrocarbons(PAHs), are highly mutagenic and carcinogenic. More researchers have paid particular attention to them. Using air and steam as gasification medium, the experiments of three kinds of coals were carried out in a bench-scale atmospheric fluidized bed gasifier. The contents of the 16 PAHs specified by US EPA in raw coal, slag, bag house coke, cyclone coke and gas were measured by HPLC to study the contents of PAHs in raw coal and the effects of the inherent characters of coals on the formation and release of PAHs in coal gasification. The experimental results showed that the distributions of PAHs in the gasified products are similar to raw coals and the total-PAHs content in coal gasification is higher than in raw coal(except Coal C). The total-PAHs contents increase and then decrease with the rise of fixed carbon and sulfur of coal while there has an opposite variation when volatile matters content increase. The quantities of PAHs reduce with the increase of ash content or the drop of heating value during coal gasification.

  4. Source and deposition of polycyclic aromatic hydrocarbons to Shanghai, China

    Institute of Scientific and Technical Information of China (English)

    Lili Yan; Xiang Li; Jianmin Chen; Xinjun Wang; Jianfei Du; Lin Ma

    2012-01-01

    Despite recent efforts to investigate the distribution and fate of polycyclic aromatic hydrocarbons (PAHs) in air,water,and soil,very little is known about their temporal change in wet deposition.As a result of increased attention to public health,a large-scale survey on the deposition flux and distribution of PAH contamination in rainwater was urgently conducted in Shanghai,China.In this study,163 rainwater samples were collected from six sites,and 15 PAH compounds were detected by the use of a simple solid phase microextraction (SPME) technique coupled with gas chromatography-mass spectrometry.The dominant PAH species monitored were naphthalene,phenanthrene,anthracene,and fluoranthene.The concentration of total PAHs per event was between 74 and 980 ng/L,with an average value of 481 ng/L,which is at the high end of worldwide figures.The annual deposition flux of PAHs in rainwater was estimated to be 4148 kg/yr in the Shanghai area,suggesting rainfall as a major possible pathway for removing PAHs from the atmosphere.Diagnostic analysis by the ratios of An/178 and F1/F1+Py suggested that combustion of grass,wood,and coal was the major contributor to PAHs in the Shanghai region.Back trajectory analysis also indicated that the pollutant sources could be from the southern part of China.

  5. Pollutants in Hong Kong soils: polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Chung, M K; Hu, R; Cheung, K C; Wong, M H

    2007-03-01

    An extensive soil survey was carried out to study the polycyclic aromatic hydrocarbon (PAH) contaminations in 138 soil samples collected throughout Hong Kong. Results demonstrated that there were low levels of PAH contaminations (median of summation operator 16US EPA PAHs=140 microg kg(-1)) for all land uses (urban park, greening area, country park, rural area, restored landfill, agricultural farmland, orchard farm, crematorium, industrial and near highway area). However, localized hotspots were identified with summation operator 16PAH concentrations as high as 19,500 microg kg(-1) in one urban park. These findings were also confirmed by multivariate analysis. Comparison of PAH profiles showed a widespread domination of its 4-ring member. The major contribution was vehicular emissions from petroleum, and however at the hotspots, the improper disposal of used motor oils. In general, the pollution levels for all the land uses were below the recommended values for residential and general purposes stated in soil quality guidelines such as Netherlands and Denmark except certain identified hotspots. The potential health hazards imposed by these hotspots were alarming, and their existence (3 out of 138 samples) suggested that sole monitoring of atmospheric PAHs may not adequately address the hidden risks to human in urban city. PMID:17109918

  6. Ecological effect of airborne particulate matter on plants

    Directory of Open Access Journals (Sweden)

    Santosh Kumar Prajapati

    2012-03-01

    Full Text Available Atmospheric particulate matter is a mixture of diverse elements. Deposition of particulate matter to vegetated surfaces depends on the size distribution of these particles and, to a lesser extent, on the chemistry. Effects of particulate matter on vegetation may be associated with the reduction in light required for photosynthesis and an increase in leaf temperature due to changed surface optical properties. Changes in energy exchange are more important than the diffusion of gases into and out of leaves which is influenced by dust load, color and particle size. Alkaline dust materials may cause leaf surface injury while other materials may be taken up across the cuticle. A more probable route for metabolic uptake and impact on vegetation and ecosystems is through the rhizosphere. Interception of dusts by vegetation makes an important contribution to the improvement of air quality in the vicinity of vegetation. Although the effect of particulate matter on ecosystem is linked to climate change, there is little threat due to un-speciated particulate matter on a regional scale.

  7. Impact of erosion and transfer processes in Polycyclic Aromatic Hydrocarbon contamination of water bodies in the Seine River basin (France)

    Science.gov (United States)

    Gateuille, David; Evrard, Olivier; Moreau-Guigon, Elodie; Chevreuil, Marc; Mouchel, Jean-Marie

    2014-05-01

    Polycyclic Aromatic Hydrocarbons (PAHs) reach problematic concentrations in water and sediment of numerous streams of the world. In the Seine River (France), they prevent to achieve the good chemical status enforced by European law. However, the provenance and the fate of PAHs found in rivers are still poorly understood. Here, we combined chemical and fallout radionuclide measurements conducted on a large number of suspended sediment (SS) (n = 231) and soil (n = 37) samples collected at 62 sites during an entire hydrological year. A model was developed to estimate mean PAH concentration in sediment from the population density in the drainage area and good relationships were found during both low stage and flood periods. Influence of human population also appeared to be stronger during the latter period. However, some discrepancies between measured and modeled PAH concentrations were observed and the role of the origin of SS was investigated. During the low flow period, the observed differences were explained by the provenance of river sediment (agricultural topsoil vs. eroded channel banks). Time-averaged PAH concentrations measured in suspended sediment collected in the catchments where erosion of agricultural topsoil dominated were systematically higher than the predicted values. On the contrary, in the catchments where erosion mainly occurred in deep soil or river embankment, the supply of particles protected from atmospheric fallout contamination led to measure concentrations below the predicted values. As this relationship between population density and SS contamination was no longer valid during the flood period, the role of transfer times was also investigated. The percentages of freshly eroded sediment in samples were determined by comparing the 7Be/210Pb ratio in rainfall and SS. An annual turn-over cycle of sediment was observed but no relationship was found between PAH contamination and residence times of particles within rivers. This result suggested

  8. Spatiotemporal analysis and human exposure assessment on polycyclic aromatic hydrocarbons in indoor air, settled house dust, and diet: A review.

    Science.gov (United States)

    Ma, Yuning; Harrad, Stuart

    2015-11-01

    This review summarizes the published literature on the presence of polycyclic aromatic hydrocarbons (PAH) in indoor air, settled house dust, and food, and highlights geographical and temporal trends in indoor PAH contamination. In both indoor air and dust, ΣPAH concentrations in North America have decreased over the past 30 years with a halving time of 6.7±1.9years in indoor air and 5.0±2.3 years in indoor dust. In contrast, indoor PAH concentrations in Asia have remained steady. Concentrations of ΣPAH in indoor air are significantly (pAmerica. In studies recording both vapor and particulate phases, the global average concentration in indoor air of ΣPAH excluding naphthalene is between 7 and 14,300 ng/m(3). Over a similar period, the average ΣPAH concentration in house dust ranges between 127 to 115,817ng/g. Indoor/outdoor ratios of atmospheric concentrations of ΣPAH have declined globally with a half-life of 6.3±2.3 years. While indoor/outdoor ratios for benzo[a]pyrene toxicity equivalents (BaPeq) declined in North America with a half-life of 12.2±3.2 years, no significant decline was observed when data from all regions were considered. Comparison of the global database, revealed that I/O ratios for ΣPAH (average=4.3±1.3), exceeded significantly those of BaPeq (average=1.7±0.4) in the same samples. The significant decline in global I/O ratios suggests that indoor sources of PAH have been controlled more effectively than outdoor sources. Moreover, the significantly higher I/O ratios for ΣPAH compared to BaPeq, imply that indoor sources of PAH emit proportionally more of the less carcinogenic PAH than outdoor sources. Dietary exposure to PAH ranges from 137 to 55,000 ng/day. Definitive spatiotemporal trends in dietary exposure were precluded due to relatively small number of relevant studies. However, although reported in only one study, PAH concentrations in Chinese diets exceeded those in diet from other parts of the world, a pattern consistent with

  9. 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

  10. Spacecraft Cabin Particulate Monitor Project

    Data.gov (United States)

    National Aeronautics and Space Administration — We propose to design, build and test an optical extinction monitor for the detection of spacecraft cabin particulates. This monitor will be sensitive to particle...

  11. Spacecraft Cabin Particulate Monitor Project

    Data.gov (United States)

    National Aeronautics and Space Administration — We have built and tested an optical extinction monitor for the detection of spacecraft cabin particulates. This sensor sensitive to particle sizes ranging from a...

  12. 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.

  13. A multivariate receptor modeling study of air-borne particulate PAHs: Regional contributions in a roadside environment.

    Science.gov (United States)

    Kim, Bong Mann; Lee, Seung-Bok; Kim, Jin Young; Kim, Sunwha; Seo, Jihoon; Bae, Gwi-Nam; Lee, Ji Yi

    2016-02-01

    Understanding the geographic source contributions by particulate polycyclic aromatic hydrocarbons (PAHs) is important for the Korean peninsula due to its downwind location from source areas. Regional influence of particulate PAHs was previously identified using diagnostic ratios applied to mobile source dominated roadside sampling data (Kim et al., 2012b). However, no study has yet been conducted to quantify the regional source contributions. We applied a multivariate receptor modeling tool to identify and quantify the regional source contributions to particulate PAHs in Seoul. Sampling of roadside particulate PAHs was conducted in Seoul, Korea for four years between May 2005 and April 2009, and data analysis was performed with a new multivariate receptor model, Solver for Mixture Problem (SMP). The SMP model identified two sources, local mobile source and transported regional source, and quantified their source contributions. Analysis of the particulate PAHs data reveals three types of episodic periods: a high regional source contribution period with one case, a high mobile source contribution period with three cases, and a normal contribution period with eight cases. Four-year average particulate PAHs source contributions from the two sources are 4.6 ng m(-3) and 10.7 ng m(-3) for regional and mobile sources, respectively and equivalent to 30% and 70% of the total estimated contribution from each of these sources. PMID:26473551

  14. Chemical characteristic of respirable particulates

    International Nuclear Information System (INIS)

    Respirable particulates are particulates which having diameter size at 2-5 µm, due to aerodynamically may be inhaled through respiratory tract and having ability to deposit into lungs, causing damage of the alveolar tissues and inducing health problems. Health Department of Bandung have reported that prevalency of acute respiratory tract infection disease having increasing tendency every year. Measurement of PM10 in period of 2002-2005 have done by BPLH Bandung city which pointed that in some places the concentration of PM10 was higher than daily threshold limit values. This research having intend to understand of respirable particulates exposure in society with characterization of chemical materials contained as hazard identification. Location of research have done in four regions of Bandung City. Personal sampler has used for collection of respirable particulates from human breathing zone. Chemical characteristic were done using neutron activation analysis, atomic absorption spectrometer and reflectance methods. The useful of this procedure as the baseline to calculate IEC (Inhalation Exposure Concentration) values for estimate the exposure of respirable particulates which inhaled during period of time. Calculating of IEC is the earlier step from epidemiological study or risk assessment which connecting prevalency of tract respiratory disease with characteristic of respirable particulates. Elements Br, Mn, Al, I, V, Cl, Ti, Na, Hg, Pb, and black carbon (BC), are the elements which identified. The results showed that respirable particulates which inhaled by citizen as receptor at Tegalega, Aria Graha, Dago Pakar, and Cisaranten Wetan are relatively higher than PM2,5 ambient air at the same places. Almost whole of such elements which contained in respirable particulates was found in highest concentration at Cisaranten Wetan. (author)

  15. A double isotope dilution method for assaying of polycyclic aromatic hydrocarbons in cigarette smoke condensate

    International Nuclear Information System (INIS)

    This report describes a double isotope dilution method for analysis of the polycyclic aromatic hydrocarbons (PAH) phenanthrene, fluor-anthene, pyrene, and benzo[a]pyrene in cigarette smoke particulates. The first isotope dilution used deuterated analogues of the first three PAH as internal standards. The second isotope dilution, for benzo[a]pyrene, used the tritiated analogue as an internal standard. The PAH were isolated from extracts of cigarette smoke particulates using a two-step procedure based on selective extraction from aqueous dimethyl sulfoxide (DMSO) followed by chromatography on silica gel extraction columns. After isolation, aliquots of the samples were analyzed for phenanthrene, pyrene, and fluoranthene by gas chromatography with mass spectrometric detection (GC/MS). Separate aliquots of the samples were analyzed for benzo[a]pyrene by high pressure liquid chromatography with fluorescence detection followed by liquid scintillation spectrometry. PAH levels from cigarette smoke condensates collected from different exposure modes were compared; no exposure-related differences were found. (author)

  16. Method for treating a particulate nuclear fuel material

    International Nuclear Information System (INIS)

    A method is given for treating particulate uranium compositions containing ammonium diuranate precursors such as uranyl fluoride and uranyl nitrate to remove the ammonium diuranate precursors. The oxide composition is contacted with sufficient ammonium hydroxide solution to convert the ammonium diruanate precursors to ammonium diuranate. The composition is then heated under a controlled atmosphere at a temperature sufficient to dry the composition, sublime any ammonium fluoride present, and convert the ammonium diuranate to uranium dioxide

  17. Qualitative and quantitative determination of water in airborne particulate matter

    OpenAIRE

    Canepari, S.; C. Farao; E. Marconi; C. Giovannelli; C. Perrino

    2012-01-01

    This paper describes the optimization and validation of a new simple method for the quantitative determination of water in atmospheric particulate matter (PM). The analyses are performed by using a coulometric Karl-Fisher system equipped with a controlled heating device; different water contributions are separated by the application of an optimized thermal ramp (three heating steps: 50–120 °C, 120–180 °C, 180–250 °C).

    The analytical performance...

  18. Qualitative and quantitative determination of water in airborne particulate matter

    OpenAIRE

    Canepari, S.; C. Farao; E. Marconi; C. Giovannelli; C. Perrino

    2013-01-01

    This paper describes the optimization and validation of a new simple method for the quantitative determination of water in atmospheric particulate matter (PM). The analyses are performed by using a coulometric Karl-Fisher system equipped with a controlled heating device; different water contributions are separated by the application of an optimized thermal ramp (three heating steps: 50–120 °C, 120–180 °C, 180–250 °C). The analytical performance of the method was verif...

  19. Particulate Matter and Ozone: Remote Sensing and Source Attribution

    OpenAIRE

    Kim, Sungshik

    2015-01-01

    Particulate matter (PM) and tropospheric ozone are air pollutants that are harmful to human health and have broad implications for climate. Despite their importance, there remain large uncertainties related to their sources, evolution in the atmosphere, and impact downwind. In this thesis, I work to address some of these uncertainties through integrated analysis of ground, aircraft, and satellite observations and using both forward and inverse modeling approaches. A new, high-resolution d...

  20. Does glucose enhance the formation of nitrogen containing polycyclic aromatic compounds and polycyclic aromatic hydrocarbons in the pyrolysis of proline?

    Energy Technology Data Exchange (ETDEWEB)

    Phillip F. Britt; A.C. Buchanan; Clyde V. Owens, Jr.; J. Todd Skeen [Oak Ridge National Laboratory, Oak Ridge, TN (United States). Chemical and Analytical Sciences Division

    2004-08-01

    The gas-phase pyrolysis of proline, glucose, 1-((2{prime}-carboxy)pyrrolidinyl)-1-deoxy-D-fructose (the proline Amadori compound), and a 1:1 mixture by weight of proline and glucose was investigated at high temperatures (600-840{sup o}C) and short residence time (i.e. 1.0 s) in an inert atmosphere to determine if glucose or Maillard reaction products enhance the formation of nitrogen containing polycyclic aromatic compounds (N-PACs) and polycyclic aromatic hydrocarbons (PAHs) in the pyrolysis of proline. To study the gas-phase formation of N-PACs and PAHs, the substrates were sublimed into the pyrolysis furnace at 460{sup o}C. Thermogravimetric analysis showed that glucose, the proline/glucose mixture, and the proline Amadori compound undergo solid-state decomposition reactions before subliming. Thus, the substrates were pyrolyzed in two stages: at 460{sup o}C during the sublimation and at 600-840{sup o}C. At 800{sup o}C with a residence time of 1.0 s, proline produced low yields of N-PACs, such as quinoline, isoquinoline, indole, acridine, and carbazole, and PAHs, such as phenanthrene, pyrene, benz(a)anthracene, benzofluoranthene isomers, and benzo(a)pyrene. Increasing the temperature and residence time increased the yield of these products. Under similar pyrolysis conditions, the proline Amadori compound produced 2-8 fold more N-PACs and PAHs than proline. A 1:1 mixture of proline and glucose produced a similar slate of pyrolysis products as the proline Amadori compound, but it is unclear whether the proline Amadori compound was an intermediate in the reaction. In general, the proline Amadori compound produced a higher yield of N-PACs and PAHs than the proline/glucose mixture, but glucose clearly enhances the low temperature gas-phase formation of N-PACs and PAHs from the pyrolysis of proline. 56 refs., 10 figs., 3 tabs.

  1. Formation of environmentally persistent free radicals from the heterogeneous reaction of ozone and polycyclic aromatic compounds.

    Science.gov (United States)

    Borrowman, Cuyler K; Zhou, Shouming; Burrow, Timothy E; Abbatt, Jonathan P D

    2016-01-01

    In the 1980s long-lived radical species were identified in cigarette tar. Since then, environmentally persistent free radicals (EPFRs) have been observed in ambient particulate matter, and have been generated in particulate matter generated from internal combustion engines. For the first time, we measure in situ the formation and decay of EPFRs through the heterogeneous reaction of ozone and several polycyclic aromatic compounds (PAC). Solid anthracene (ANT), pyrene (PY), benzo[a]pyrene (BAP), benzo[ghi]perylene (BGHIP), 1,4-naphthoquinone (1,4NQ), and 9,10-anthraquinone (AQ) were reacted with gas-phase ozone in a flow system placed in the active cavity of an electron paramagnetic resonance (EPR) spectrometer, and the formation of radicals was measured on the timescale of tens of minutes at ambient levels of ozone down to 30 ppb. For most substrates the net radical production is initially rapid, slows at intermediate times, and is followed by a slow decay. For oxidized solid BAP, radical signal persists for many days in the absence of ozone. To evaluate the effect of substrate phase, the solid PAHs were also dissolved in squalane, an organic oil inert to ozone, which yielded a much higher maximum radical concentration and faster radical decay when exposed to ozone. With higher mobility, reactants were apparently able to more easily diffuse and react with each other, yielding the higher radical concentrations. The EPR spectra exhibit three radicals types, two of which have been assigned to semiquinone species and one to a PAH-derived, carbon-centered radical. Although our system uses levels of PAC not typically found in the environment it is worth noting that the amounts of radical formed, on the order of 10(18) radicals per g, are comparable to those observed in ambient particulate matter. PMID:26603953

  2. Receptor modelling study of polycyclic aromatic hydrocarbons in Jeddah, Saudi Arabia

    International Nuclear Information System (INIS)

    Measurements of 14 polycyclic aromatic hydrocarbons (PAH) have been made in Jeddah, Saudi Arabia, with a view to establishing the concentrations in this major city, and quantifying the contributions of major sources. Particulate and vapour forms have been sampled and analysed separately. The concentrations are compared to measurements from other sites in the Middle Eastern region and are towards the lower end of the range, being far lower than concentrations reported from Riyadh (Saudi Arabia), Assiut (Egypt) and Tehran (Iran) but broadly similar to those measured in Damascus (Syria) and higher than those measured in Kuwait. The partitioning between vapour and particle phases is similar to that in data from Egypt and China, but with many compounds showing a higher particle-associated percentage than in Birmingham (UK) possibly reflecting a higher concentration of airborne particulate matter in the former countries. Concentrations in Jeddah were significantly higher at a site close to the oil refinery and a site close to a major ring road than at a suburban site to the north of the city. Application of positive matrix factorisation to the pooled data elicited three factors accounting respectively for 17%, 33% and 50% of the measured sum of PAH and these are interpreted as arising from gasoline vehicles, industrial sources, particularly the oil refinery, and to diesel/fuel oil combustion. - Highlights: • Measurements of 14 PAH compounds in vapour and particulate phases at three sites. • Comparison of concentrations across Jeddah and Middle Eastern regions. • Application of positive matrix factorisation to identify possible sources

  3. Receptor modelling study of polycyclic aromatic hydrocarbons in Jeddah, Saudi Arabia

    Energy Technology Data Exchange (ETDEWEB)

    Alghamdi, Mansour A. [Department of Environmental Sciences, Faculty of Meteorology, Environment and Arid Land Agriculture, King Abdulaziz University, Jeddah (Saudi Arabia); Alam, Mohammed S., E-mail: m.s.alam@bham.ac.uk [Division of Environmental Health and Risk Management, School of Geography, Earth and Environmental Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT (United Kingdom); Yin, Jianxin; Stark, Christopher; Jang, Eunhwa [Division of Environmental Health and Risk Management, School of Geography, Earth and Environmental Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT (United Kingdom); Harrison, Roy M., E-mail: r.m.harrison@bham.ac.uk [Department of Environmental Sciences, Faculty of Meteorology, Environment and Arid Land Agriculture, King Abdulaziz University, Jeddah (Saudi Arabia); Division of Environmental Health and Risk Management, School of Geography, Earth and Environmental Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT (United Kingdom); Shamy, Magdy; Khoder, Mamdouh I.; Shabbaj, Ibrahim I. [Department of Environmental Sciences, Faculty of Meteorology, Environment and Arid Land Agriculture, King Abdulaziz University, Jeddah (Saudi Arabia)

    2015-02-15

    Measurements of 14 polycyclic aromatic hydrocarbons (PAH) have been made in Jeddah, Saudi Arabia, with a view to establishing the concentrations in this major city, and quantifying the contributions of major sources. Particulate and vapour forms have been sampled and analysed separately. The concentrations are compared to measurements from other sites in the Middle Eastern region and are towards the lower end of the range, being far lower than concentrations reported from Riyadh (Saudi Arabia), Assiut (Egypt) and Tehran (Iran) but broadly similar to those measured in Damascus (Syria) and higher than those measured in Kuwait. The partitioning between vapour and particle phases is similar to that in data from Egypt and China, but with many compounds showing a higher particle-associated percentage than in Birmingham (UK) possibly reflecting a higher concentration of airborne particulate matter in the former countries. Concentrations in Jeddah were significantly higher at a site close to the oil refinery and a site close to a major ring road than at a suburban site to the north of the city. Application of positive matrix factorisation to the pooled data elicited three factors accounting respectively for 17%, 33% and 50% of the measured sum of PAH and these are interpreted as arising from gasoline vehicles, industrial sources, particularly the oil refinery, and to diesel/fuel oil combustion. - Highlights: • Measurements of 14 PAH compounds in vapour and particulate phases at three sites. • Comparison of concentrations across Jeddah and Middle Eastern regions. • Application of positive matrix factorisation to identify possible sources.

  4. Group and ring theoretic properties of polycyclic groups

    CERN Document Server

    Wehrfritz, BAF

    2009-01-01

    Polycyclic groups are built from cyclic groups in a specific way. They arise in many contexts within group theory itself but also more generally in algebra, for example in the theory of Noetherian rings. The first half of this book develops the standard group theoretic techniques for studying polycyclic groups and the basic properties of these groups. The second half then focuses specifically on the ring theoretic properties of polycyclic groups and their applications, often to purely group theoretic situations. The book is intended to be a study manual for graduate students and researchers co

  5. The particulate matter dispersion studies from a local palm oil mill

    International Nuclear Information System (INIS)

    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)

  6. 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.

  7. Hydrocarbon-enhanced particulate filter regeneration via microwave ignition

    Science.gov (United States)

    Gonze, Eugene V.; Brown, David B.

    2010-02-02

    A regeneration method for a particulate filter includes estimating a quantity of particulate matter trapped within the particulate filter, comparing the quantity of particulate matter to a predetermined quantity, heating at least a portion of the particulate filter to a combustion temperature of the particulate matter, and introducing hydrocarbon fuel to the particulate filter. The hydrocarbon fuel facilitates combustion of the particulate matter to regenerate the particulate filter.

  8. Size-distribution of airborne polycyclic aromatic hydrocarbons and other organic source markers in the surroundings of a cement plant powered with alternative fuels.

    Science.gov (United States)

    Sánchez-Soberón, Francisco; van Drooge, Barend L; Rovira, Joaquim; Grimalt, Joan O; Nadal, Martí; Domingo, José L; Schuhmacher, Marta

    2016-04-15

    The distributions of polycyclic aromatic hydrocarbons (PAHs) and molecular tracer organic compounds for biomass combustion, traffic emissions, soil dust, and secondary aerosol processing have been studied in three fractions of ambient air particulate matter (PM10, 2.5, and 1) collected in the vicinity of a cement plant. PAH concentrations were used to estimate the carcinogenic risks in humans. Combustion related compounds, including PAHs, and those from secondary aerosol processing, predominated in the finest (PMlaw. Exposure and inhalation carcinogenic risks from total PAHs were below the EPA threshold of acceptable risk (1·10(-6)). PMID:26859698

  9. Provisional Guidance for Quantitative Risk Assessment of Polycyclic Aromatic Hydrocarbons

    Science.gov (United States)

    Polycyclic Aromatic Hydrocarbons (PAHs) are products of incomplete combustion of organic materials; sources are, thus, widespread,including cigarette smoke, municipal waste incineration, wood stove emissions, coal conversion, energy production form fossil fuels, and automobile an...

  10. Physical-chemical characterisation of the particulate matter inside two road tunnels in the São Paulo Metropolitan Area

    Science.gov (United States)

    Brito, J.; Rizzo, L. V.; Herckes, P.; Vasconcellos, P. C.; Caumo, S. E. S.; Fornaro, A.; Ynoue, R. Y.; Artaxo, P.; Andrade, M. F.

    2013-12-01

    The notable increase in biofuel usage by the road transportation sector in Brazil during recent years has significantly altered the vehicular fuel composition. Consequently, many uncertainties are currently found in particulate matter vehicular emission profiles. In an effort to better characterise the emitted particulate matter, measurements of aerosol physical and chemical properties were undertaken inside two tunnels located in the São Paulo Metropolitan Area (SPMA). The tunnels show very distinct fleet profiles: in the Jânio Quadros (JQ) tunnel, the vast majority of the circulating fleet are light duty vehicles (LDVs), fuelled on average with the same amount of ethanol as gasoline. In the Rodoanel (RA) tunnel, the particulate emission is dominated by heavy duty vehicles (HDVs) fuelled with diesel (5% biodiesel). In the JQ tunnel, PM2.5 concentration was on average 52 μg m-3, with the largest contribution of organic mass (OM, 42%), followed by elemental carbon (EC, 17%) and crustal elements (13%). Sulphate accounted for 7% of PM2.5 and the sum of other trace elements was 10%. In the RA tunnel, PM2.5 was on average 233 μg m-3, mostly composed of EC (52%) and OM (39%). Sulphate, crustal and the trace elements showed a minor contribution with 5%, 1%, and 1%, respectively. The average OC : EC ratio in the JQ tunnel was 1.59 ± 0.09, indicating an important contribution of EC despite the high ethanol fraction in the fuel composition. In the RA tunnel, the OC : EC ratio was 0.49 ± 0.12, consistent with previous measurements of diesel-fuelled HDVs. Besides bulk carbonaceous aerosol measurement, polycyclic aromatic hydrocarbons (PAHs) were quantified. The sum of the PAHs concentration was 56 ± 5 ng m-3 and 45 ± 9 ng m-3 in the RA and JQ tunnel, respectively. In the JQ tunnel, benzo(a)pyrene (BaP) ranged from 0.9 to 6.7 ng m-3 (0.02-0.1‰ of PM2.5) whereas in the RA tunnel BaP ranged from 0.9 to 4.9 ng m-3 (0.004-0. 02‰ of PM2.5), indicating an important

  11. Physical-chemical characterization of the particulate matter inside two road tunnels in the São Paulo Metropolitan Area

    Science.gov (United States)

    Brito, J.; Rizzo, L. V.; Herckes, P.; Vasconcellos, P. C.; Caumo, S. E. S.; Fornaro, A.; Ynoue, R. Y.; Artaxo, P.; Andrade, M. F.

    2013-08-01

    The notable increase in biofuel usage by the road transportation sector in Brazil during recent years has significantly altered the vehicular fuel composition. Consequently, many uncertainties are currently found in particulate matter vehicular emission profiles. In an effort to better characterize the emitted particulate matter, measurements of aerosol physical and chemical properties were undertaken inside two tunnels located in the São Paulo Metropolitan Area (SPMA). The tunnels show very distinct fleet profiles: in the Jânio Quadros (JQ) tunnel, the vast majority of the circulating fleet are Light Duty Vehicles (LDVs), fuelled on average with the same amount of ethanol as gasoline. In the Rodoanel (RA) tunnel, the particulate emission is dominated by Heavy Duty Vehicles (HDVs) fuelled with diesel (5% biodiesel). In the JQ tunnel, PM2.5 concentration was on average 52 μg m-3, with the largest contribution of Organic Mass (OM, 42%), followed by Elemental Carbon (EC, 17%) and Crustal elements (13%). Sulphate accounted for 7% of PM2.5 and the sum of other trace elements was 10%. In the RA tunnel, PM2.5 was on average 233 μg m-3, mostly composed of EC (52%) and OM (39%). Sulphate, crustal and the trace elements showed a minor contribution with 5%, 1% and 1%, respectively. The average OC:EC ratio in the JQ tunnel was 1.59 ± 0.09, indicating an important contribution of EC despite the high ethanol fraction in the fuel composition. In the RA tunnel, the OC:EC ratio was 0.49 ± 0.12, consistent with previous measurements of diesel fuelled HDVs. Besides bulk carbonaceous aerosol measurement, Polycyclic Aromatic Hydrocarbons (PAHs) were quantified. The sum of the PAHs concentration was 56 ± 5 ng m-3 and 45 ± 9 ng m-3 in the RA and JQ tunnel, respectively. In the JQ tunnel, Benzo(a)pyrene (BaP) ranged from 0.9 to 6.7 ng m-3 (0.02-0.1‰ of PM2.5) in the JQ tunnel whereas in the RA tunnel BaP ranged from 0.9 to 4.9 ng m-3 (0.004-0.02‰ of PM2.5), indicating an

  12. Physical-chemical characterization of the particulate matter inside two road tunnels in the São Paulo Metropolitan Area

    Directory of Open Access Journals (Sweden)

    J. Brito

    2013-08-01

    Full Text Available The notable increase in biofuel usage by the road transportation sector in Brazil during recent years has significantly altered the vehicular fuel composition. Consequently, many uncertainties are currently found in particulate matter vehicular emission profiles. In an effort to better characterize the emitted particulate matter, measurements of aerosol physical and chemical properties were undertaken inside two tunnels located in the São Paulo Metropolitan Area (SPMA. The tunnels show very distinct fleet profiles: in the Jânio Quadros (JQ tunnel, the vast majority of the circulating fleet are Light Duty Vehicles (LDVs, fuelled on average with the same amount of ethanol as gasoline. In the Rodoanel (RA tunnel, the particulate emission is dominated by Heavy Duty Vehicles (HDVs fuelled with diesel (5% biodiesel. In the JQ tunnel, PM2.5 concentration was on average 52 μg m−3, with the largest contribution of Organic Mass (OM, 42%, followed by Elemental Carbon (EC, 17% and Crustal elements (13%. Sulphate accounted for 7% of PM2.5 and the sum of other trace elements was 10%. In the RA tunnel, PM2.5 was on average 233 μg m−3, mostly composed of EC (52% and OM (39%. Sulphate, crustal and the trace elements showed a minor contribution with 5%, 1% and 1%, respectively. The average OC:EC ratio in the JQ tunnel was 1.59 ± 0.09, indicating an important contribution of EC despite the high ethanol fraction in the fuel composition. In the RA tunnel, the OC:EC ratio was 0.49 ± 0.12, consistent with previous measurements of diesel fuelled HDVs. Besides bulk carbonaceous aerosol measurement, Polycyclic Aromatic Hydrocarbons (PAHs were quantified. The sum of the PAHs concentration was 56 ± 5 ng m−3 and 45 ± 9 ng m−3 in the RA and JQ tunnel, respectively. In the JQ tunnel, Benzo(apyrene (BaP ranged from 0.9 to 6.7 ng m−3 (0.02–0.1‰ of PM2.5 in the JQ tunnel whereas in the RA tunnel BaP ranged from 0.9 to 4.9 ng m−3 (0.004–0.02‰ of PM2

  13. Vibrational Characterisation and Fluorescence Optimisation of Polycyclic Polymers

    OpenAIRE

    O'Neill, Luke; Lynch, Patrick; McNamara, Mary; Byrne, Hugh

    2007-01-01

    A systematic series of polycyclic novel polymers was studied by Raman spectroscopy. The effect of the sequential introduction of polycyclic aromatic ring substituents into the delocalized backbone was examined in relation to the variation of the relative ring breathing and stretching as well as the vinyl stretch frequencies. Replacement of the phenyl units by higher order acene moieties such as naphthyl and anthryl results in a shift of the characteristic stretching frequencies, and analysis ...

  14. Particulate PAHs and n-alkanes in the air over Southern and Eastern Mediterranean Sea.

    Science.gov (United States)

    Romagnoli, Paola; Balducci, Catia; Perilli, Mattia; Perreca, Erica; Cecinato, Angelo

    2016-09-01

    Particulate polycyclic aromatic hydrocarbons, n-alkanes and polar organic compounds were investigated in the marine atmosphere of Southern and Eastern Mediterranean Sea, in the frame of the scientific cruise of Urania ship between 27 July and 11 August 2013. The PM10 fraction of aerosol to which most organic substances are associated, were collected daily; contemporarily, gaseous regulated toxicants (ozone, nitrogen oxides and carbon oxide) and carbonyls were recorded. Samplings were carried out in front of Palermo and Messina, respectively the start and end harbors, and along the cruise, both in movement (transects, N = 14) and at stops (N = 11). Total PAHs ranged from 0.06 ng/m(3) up to 1.8 ng/m(3), with the maximums observed close to harbors. Unlike total concentrations that were in general comparable, the percent composition of PAHs was distinct for harbors, transects and stops, which allowed to draw insights about the pollution sources impact. Concentrations of n-alkanes (C18-C35) ranging from 6.7 to 43 ng/m(3) were quantified. The carbonyls evaluation revealed relatively high concentrations of formaldehyde (∼4-24 μg/m(3)) and acetone (∼5-35 μg/m(3)) near harbors, and of acrolein (up to 12 μg/m(3)) offshore, while benzaldehyde was quite independent of the site type (≈0.5 μg/m(3)). Nicotine and caffeine were detected, at different extents (0.0-2.2 ng/m(3) and 0.01-0.17 ng/m(3), respectively), in ca. 70% and 100% of samples. Alkyl phthalates ranged from 2.7 to 67 ng/m(3) and showed variable percentages in the samples. Finally, traces of N,N-diethyl-meta-toluene amide (up to 0.4 ng/m(3)) were found at all sites. PMID:27341155

  15. Les effets environnementaux des particules

    OpenAIRE

    Brignon, Jean-Marc

    2003-01-01

    En dehors de leur effet sur la santé humaine, les particules interviennent dans de nombreuses problématiques environnementales, dont le changement climatique, la formation d'ozone troposphérique, la réduction de la visibilité, et les régimes hydrologiques. L'effet des particules en termes de changement climatique est complexe et emprunte plusieurs voies. Il se traduit par des effets opposés de réchauffement ou de refroidissement de l'atmosphère, notamment selon la composition chimique des par...

  16. Mineralogical characterization of airborne individual particulates in Beijing PM10

    Institute of Scientific and Technical Information of China (English)

    LU Sen-lin; SHAO Long-yi; WU Ming-hong; JIAO Zheng

    2006-01-01

    This work mainly focuses on the mineralogical study of particulate matter(PM10) in Beijing. Samples were collected on polycarbonate filter from April, 2002 to March, 2003 in Beijing urban area. Scanning electronic microscopy coupled with energy dispersive X-ray(SEM/EDX) was used to investigate individual mineral particles in Beijing PM10. 1454 individual mineral particulates from 48 samples were analysed by SEM/EDX. The results revealed that mineral particulates were complex and heterogeneous. 38kinds of minerals in PM10 were identified. The clay minerals, of annual average percentage of 30.1% , were the main composition among the identified minerals, and illite/smectite was the main composition in clay minerals, reaching up to 35%. Annual average percentage of quartz, calcite, compound particulates, carbonates were 13.5%, 10.9%, 11.95%, 10.31%, respectively. Annual average percentage less than 10% were gypsum, feldspar, dolomite, and so on. Fluorite, apatite, halite, barite and chloridize zinc (ZnCl2) were firstly identified in Beijing PM10. Sulfurization was found on surface of mineral particles, suggested extensive atmospheric reaction in air during summer.

  17. Characterization of the winter midwestern particulate nitrate bulge.

    Science.gov (United States)

    Pitchford, Marc L; Poirot, Richard L; Schichtel, Bret A; Maim, William C

    2009-09-01

    A previously unobserved multi-state region of elevated particulate nitrate concentration was detected as a result of the expansion of the Interagency Monitoring of Protected Visual Environments (IMPROVE) network of remote-area particulate matter (PM) speciation monitoring sites into the midwestern United States that began in 2002. Mean winter ammonium nitrate concentrations exceed 4 microg/m3 in a region centered in Iowa, which makes it responsible for as much as half of the particle light extinction. Before these observations, particulate nitrate in the United States was only observed to be a dominant component of the fine PM (PM2.5) in parts of California and some urban areas. Comparisons of the spatial patterns of particulate nitrate with spatial patterns of ammonia and nitrogen oxide emissions suggest that the nitrate bulge is the result of the high emissions of ammonia associated with animal agriculture in the Midwest. Nitrate episodes at several locations in the eastern United States are shown to be associated with transport pathways over the Midwest, suggesting long-range transport of either ammonia or ammonium nitrate. Thermodynamic equilibrium modeling conducted by others on data from the Midwest shows the relative importance of atmospheric ammonia and nitric acid in the production of PM2.5. This is a particular concern as the sulfur dioxide emissions in the United States are reduced, which increases the amount of ammonia available for ammonium nitrate production. PMID:19785273

  18. [Characteristic of Particulate Emissions from Concrete Batching in Beijing].

    Science.gov (United States)

    Xue, Yi-feng; Zhou, Zhen; Zhong, Lian-hong; Yan, Jing; Qu, Song; Huang, Yu-hu; Tian, He- zhong; Pan, Tao

    2016-01-15

    With the economic development and population growth in Beijing, there is a strong need for construction and housing, which leads to the increase of the construction areas. Meanwhile, as a local provided material, the production of concrete has been raised. In the process of concrete production by concrete batching, there are numerous particulates emitted, which have large effect on the atmospheric environment, however, systematic study about the tempo-spatial characteristics of pollutant emission from concrete batching is still rare. In this study, we estimated the emission of particulates from concrete batching from 1991 to 2012 using emission factor method, analyzed the tempo-spatial characteristics of pollutant emission, established the uncertainty range by adopting Monte-Carlo method, and predicted the future emission in 2020 based on the relative environmental and economical policies. The results showed that: (1) the emissions of particulates from concrete batching showed a trend of "first increase and then decrease", reaching the maximum in 2005, and then decreased due to stricter emission standard and enhanced environmental management. (2) according to spatial distribution, the emission of particulates from concrete batch mainly concentrated in the urban area with more human activities, and the area between the fifth ring and the sixth ring contributed the most. (3) through scenarios analysis, for further reducing the emission from concrete batching in 2020, more stricter standard for green production as well as powerful supervision is needed. PMID:27078945

  19. Terrestrial mosses as biomonitors of atmospheric POPs pollution: a review

    OpenAIRE

    Harmens, H.; Foan, L.; Simon, V; Mills, G.

    2013-01-01

    Worldwide there is concern about the continuing release of persistent organic pollutants (POPs) into the environment. In this study we review the application of mosses as biomonitors of atmospheric deposition of POPs. Examples in the literature show that mosses are suitable organisms to monitor spatial patterns and temporal trends of atmospheric concentrations or deposition of POPs. These examples include polycyclic aromatic hydrocarbons (PAHs), polychlorobiphenyls (PCBs), dioxins and furans ...

  20. CDC WONDER: Daily Fine Particulate Matter

    Data.gov (United States)

    U.S. Department of Health & Human Services — The Daily Fine Particulate Matter data available on CDC WONDER are geographically aggregated daily measures of fine particulate matter in the outdoor air, spanning...

  1. Transport phenomena in particulate systems

    CERN Document Server

    Freire, José Teixeira; Ferreira, Maria do Carmo

    2012-01-01

    This volume spans 10 chapters covering different aspects of transport phenomena including fixed and fluidized systems, spouted beds, electrochemical and wastewater treatment reactors. This e-book will be valuable for students, engineers and researchers aiming to keep updated on the latest developments on particulate systems.

  2. Solubilities of solid polycyclic aromatic hydrocarbons and polycyclic aromatic heterocycles in pressurized hot water

    Czech Academy of Sciences Publication Activity Database

    Karásek, Pavel; Planeta, Josef; Roth, Michal

    Boulder, CO: National Institute of Standards and Technology, 325 Broadway, Boulder, CO 80305, USA, 2006 - (Friend, D.; Frenkel, M.; Muzny, C.; Hardin, G.). s. 641-642 [International Conference on Chemical Thermodynamics /19./. THERMO International 2006. 30.07.2006-04.08.2006, Boulder, CO] R&D Projects: GA AV ČR IAA4031301; GA AV ČR KJB400310504; GA ČR GA203/05/2106 Keywords : aqueous solubility * pressurized hot water * polycyclic aromatic compounds Subject RIV: CF - Physical ; Theoretical Chemistry

  3. High atmosphere-ocean exchange of semivolatile aromatic hydrocarbons

    Science.gov (United States)

    González-Gaya, Belén; Fernández-Pinos, María-Carmen; Morales, Laura; Méjanelle, Laurence; Abad, Esteban; Piña, Benjamin; Duarte, Carlos M.; Jiménez, Begoña; Dachs, Jordi

    2016-06-01

    Polycyclic aromatic hydrocarbons, and other semivolatile aromatic-like compounds, are an important and ubiquitous fraction of organic matter in the environment. The occurrence of semivolatile aromatic hydrocarbons is due to anthropogenic sources such as incomplete combustion of fossil fuels or oil spills, and other biogenic sources. However, their global transport, fate and relevance for the carbon cycle have been poorly assessed, especially in terms of fluxes. Here we report a global assessment of the occurrence and atmosphere-ocean fluxes of 64 polycyclic aromatic hydrocarbons analysed in paired atmospheric and seawater samples from the tropical and subtropical Atlantic, Pacific and Indian oceans. The global atmospheric input of polycyclic aromatic hydrocarbons to the global ocean is estimated at 0.09 Tg per month, four times greater than the input from the Deepwater Horizon spill. Moreover, the environmental concentrations of total semivolatile aromatic-like compounds were 102-103 times higher than those of the targeted polycyclic aromatic hydrocarbons, with a relevant contribution of an aromatic unresolved complex mixture. These concentrations drive a large global deposition of carbon, estimated at 400 Tg C yr-1, around 15% of the oceanic CO2 uptake.

  4. Distribution of polycyclic aromatic hydrocarbons in surface water from the upper reach of the Yellow River, Northwestern China.

    Science.gov (United States)

    Zhao, Xia; Qiu, Haoran; Zhao, Yangli; Shen, Jimin; Chen, Zhonglin; Chen, Jixiang

    2015-05-01

    The concentrations of 16 polycyclic aromatic hydrocarbons (PAHs) in water, suspended particulate matters (SPMs), and sediments in the Lanzhou reach of the Yellow River were investigated in this study. The total PAH concentrations ranged from 548 to 2598 ng/L in water, 1502 to 11,562 ng/g in SPMs, and 181 to 1583 ng/g in sediments. The compositions of PAHs showed that 2- to 3-ring PAHs were abundant in water, 2- to 4-ring PAHs were predominant in SPMs, and 2- to 5-ring PAHs were abundant in sediments. The spatial distribution of PAHs was site-specific and PAHs varied at different sampling locations. The diagnostic ratio analysis indicated that the PAHs mainly had a pyrolytic source. The ecological risk assessment showed that the ecosystem risk of PAHs was low in the Lanzhou reach of the Yellow River. PMID:25475612

  5. Porphyrins Fused with Unactivated Polycyclic Aromatic Hydrocarbons

    KAUST Repository

    Diev, Vyacheslav V.

    2012-01-06

    A systematic study of the preparation of porphyrins with extended conjugation by meso,β-fusion with polycyclic aromatic hydrocarbons (PAHs) is reported. The meso-positions of 5,15-unsubstituted porphyrins were readily functionalized with PAHs. Ring fusion using standard Scholl reaction conditions (FeCl 3, dichloromethane) occurs for perylene-substituted porphyrins to give a porphyrin β,meso annulated with perylene rings (0.7:1 ratio of syn and anti isomers). The naphthalene, pyrene, and coronene derivatives do not react under Scholl conditions but are fused using thermal cyclodehydrogenation at high temperatures, giving mixtures of syn and anti isomers of the meso,β-fused porphyrins. For pyrenyl-substituted porphyrins, a thermal method gives synthetically acceptable yields (>30%). Absorption spectra of the fused porphyrins undergo a progressive bathochromic shift in a series of naphthyl (λ max = 730 nm), coronenyl (λ max = 780 nm), pyrenyl (λ max = 815 nm), and perylenyl (λ max = 900 nm) annulated porphyrins. Despite being conjugated with unsubstituted fused PAHs, the β,meso-fused porphyrins are more soluble and processable than the parent nonfused precursors. Pyrenyl-fused porphyrins exhibit strong fluorescence in the near-infrared (NIR) spectral region, with a progressive improvement in luminescent efficiency (up to 13% with λ max = 829 nm) with increasing degree of fusion. Fused pyrenyl-porphyrins have been used as broadband absorption donor materials in photovoltaic cells, leading to devices that show comparatively high photovoltaic efficiencies. © 2011 American Chemical Society.

  6. [Polycyclic aromatic hydrocarbons exposure and birth defects].

    Science.gov (United States)

    Lin, S S; Huang, Y; Wang, C Y; Ren, A G

    2016-06-01

    Birth defects are one of the most common adverse birth outcomes, which create a heavy economic burden to the country, society and family. And they are also one of the biggest problems facing public health today. Polycyclic aromatic hydrocarbons (PAHs) are a group of toxic pollutants existing in the environment widely, resulting from incomplete organic matter combustion, and can be taken into the body through various ways including the digestive tract, respiratory tract and so on. Recent researches suggest that the exposure of PAHs may be associated with various birth defects, while the special mechanism isn't very clear. This paper is a review of the relationship between PAHs and birth defects from the aspects of epidemiological data, experimental evidence on animals, which indicates that exposure of PAHs during pregnancy may be associated with birth defects including congenital heart defects, neural tube defects and cleft lip/plate. Furthermore, we explored the possible mechanism, including oxidative stress, oxidative damage and the changes of signal transduction pathway in order to provide some recommendations and suggestions on the future work. PMID:27256742

  7. Polycyclic aromatic hydrocarbon molecules in astrophysics

    Science.gov (United States)

    Rastogi, Shantanu; Pathak, Amit; Maurya, Anju

    2013-06-01

    Polycyclic aromatic hydrocarbon (PAH) molecules are responsible for the mid-infrared emission features. Their ubiquitous presence in almost all types of astrophysical environments and related variations in their spectral profilesmake them an important tool to understand the physics and chemistry of the interstellar medium. The observed spectrum is generally a composite superposition of all different types of PAHs possible in the region. In the era of space telescopes the spectral richness of the emission features has enhanced their importance as probe and also the need to understand the variations with respect to PAH size, type and ionic state. Quantum computational studies of PAHs have proved useful in elucidating the profile variations and put constraints on the possible types of PAHs in different environments. The study of PAHs has also significantly contributed to the problems of diffuse interstellar bands (DIBs), UV extinction and understanding the chemistry of the formation of complex organics in space. The review highlights the results of various computational models for the understanding of infrared emission features, the PAH-DIB relation, formation of prebiotics and possible impact in the understanding of far-infrared features.

  8. Factors affecting the level and pattern of polycyclic aromatic hydrocarbons (PAHs) at Gosan, Korea during a dust period

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Sung-Deuk [School of Urban and Environmental Engineering, Ulsan National Institute of Science and Technology (UNIST), 100, Banyeon-ri, Eonyang-eup, Ulsan 689-798 (Korea, Republic of); Ghim, Young Sung, E-mail: ysghim@hufs.ac.kr [Department of Environmental Science, Hankuk University of Foreign Studies, Wangsan-ri, Mohyeon-myeon, Yongin 449-791 (Korea, Republic of); Lee, Ji Yi [Department of Environmental Engineering, BK21 Team for Biohydrogen Production, Chosun University, 375 Seosuk-dong, Dong-gu, Gwangju 501-759 (Korea, Republic of); Kim, Jin Young [Center for Environmental Technology Research, Korea Institute of Science and Technology (KIST), Seoul 136-791 (Korea, Republic of); Kim, Yong Pyo [Department of Environmental Science and Engineering, Ewha Womans University, 11-1 Daehyun-dong, Seodaemun-gu, Seoul 120-750 (Korea, Republic of)

    2012-08-15

    Highlights: Black-Right-Pointing-Pointer We collected air samples at a remote site during an Asian dust period. Black-Right-Pointing-Pointer We analyzed levels, patterns, and gas/particle partitioning of PAHs. Black-Right-Pointing-Pointer Particulate PAHs were highly correlated with PM{sub 2.5}. Black-Right-Pointing-Pointer The fraction of particulate PAHs increased during the dust period. Black-Right-Pointing-Pointer Fine particles might be an important carrier of PAHs emitted from China. - Abstract: Polycyclic aromatic hydrocarbons (PAHs) in both gas and total suspended particles were measured at Gosan, Jeju Island in Korea, a remote background site, for 15 days (March 29-April 12, 2002). During the sampling period, a severe three-day Asian dust (AD) event originating from Mongolia and northern China was observed throughout the Korean Peninsula and Jeju Island. In addition, pollution (PO) and normal (NO) periods were also identified based on the levels of anthropogenic pollutants. Despite a large difference of PM{sub 10} concentrations between the AD and PO periods, the levels of particulate PAHs in both periods were comparable (2.7 {+-} 1.0 and 2.4 {+-} 0.5 ng m{sup -3}, respectively) since they were determined by the concentration of anthropogenic PM{sub 2.5} transported from industrial areas of China. In the AD period, the level of gaseous PAHs, which were mostly from local sources, was the lowest due to strong winds; the gas/particle partitioning was close to equilibrium as the effect of long-range transport was manifested. The results of backward air trajectories, correlation analysis, and diagnostic ratios show that long-range transport of particulate PAHs produced by coal/biomass burning in China could strongly affect the levels and patterns of PAHs at Gosan, Korea.

  9. Factors affecting the level and pattern of polycyclic aromatic hydrocarbons (PAHs) at Gosan, Korea during a dust period

    International Nuclear Information System (INIS)

    Highlights: ► We collected air samples at a remote site during an Asian dust period. ► We analyzed levels, patterns, and gas/particle partitioning of PAHs. ► Particulate PAHs were highly correlated with PM2.5. ► The fraction of particulate PAHs increased during the dust period. ► Fine particles might be an important carrier of PAHs emitted from China. - Abstract: Polycyclic aromatic hydrocarbons (PAHs) in both gas and total suspended particles were measured at Gosan, Jeju Island in Korea, a remote background site, for 15 days (March 29–April 12, 2002). During the sampling period, a severe three-day Asian dust (AD) event originating from Mongolia and northern China was observed throughout the Korean Peninsula and Jeju Island. In addition, pollution (PO) and normal (NO) periods were also identified based on the levels of anthropogenic pollutants. Despite a large difference of PM10 concentrations between the AD and PO periods, the levels of particulate PAHs in both periods were comparable (2.7 ± 1.0 and 2.4 ± 0.5 ng m−3, respectively) since they were determined by the concentration of anthropogenic PM2.5 transported from industrial areas of China. In the AD period, the level of gaseous PAHs, which were mostly from local sources, was the lowest due to strong winds; the gas/particle partitioning was close to equilibrium as the effect of long-range transport was manifested. The results of backward air trajectories, correlation analysis, and diagnostic ratios show that long-range transport of particulate PAHs produced by coal/biomass burning in China could strongly affect the levels and patterns of PAHs at Gosan, Korea.

  10. Characteristics and cellular effects of ambient particulate matter from Beijing

    International Nuclear Information System (INIS)

    In vitro tests using human adenocarcinomic alveolar epithelial cell line A549 and small mouse monocyte-macrophage cell line J774A.1 were conducted to test toxicity of six PM (particulate matter) samples from Beijing. The properties of the samples differ significantly. The production of inflammatory cytokine (TNF-α for J774A.1) and chemokine (IL-8 for A549) and the level of intracellular reactive oxygen species (ROS) were used as endpoints. There was a positive correlation between water soluble organic carbon and DTT-based redox activity. Both cell types produced increased levels of inflammatory mediators and had higher level of intracelllar ROS, indicating the presence of PM-induced inflammatory response and oxidative stress, which were dose-dependent and significantly different among the samples. The releases of IL-8 from A549 and TNF-α from J774A.1 were significantly correlated to PM size, Zeta potential, endotoxin, major metals, and polycyclic aromatic hydrocarbons. No correlation between ROS and these properties was identified. - Highlights: • Six PMs from Beijing were tested for toxicity using A549 and J774A.1 cell lines. • The properties of the PM samples differ significantly. • Dose-dependent inflammatory response and oxidative stress were found. • The release of inflammatory cytokine was significantly correlated to PM properties. • No correlation between ROS and PM properties was identified. - Cellular toxicity of PM2.5 from Beijing depends on their properties

  11. Effect of Diesel Sulfur on the Regeneration of Catalyst based Diesel Particulate Filters

    Directory of Open Access Journals (Sweden)

    Pruthviraj S Balekai

    2013-08-01

    Full Text Available Diesel particulate filters are used in diesel engines to clean the particulate matter, which is released into the atmosphere. These particulate filters have a mechanism, which is affected by diesel sulfur level. My study refers to the effect with which the sulfur in diesel affects the regeneration rate of the diesel particulate filters. Two filters with different coatings were taken. Diesel Sulfur with different concentrations was tested. It was observed that there was linear relation between sulfur level and balance point temperature. Also, it was observed that this was the cause for not using full-blend biodiesel, as the emission standards could not be met due to high sulfur levels in the biodiesel.

  12. Current state of particulate matter research and management in Serbia (Introductory paper

    Directory of Open Access Journals (Sweden)

    Milena Jovašević-Stojanović

    2010-09-01

    Full Text Available Particulate matter is the air pollutant that currently receives most attention from the atmospheric research community, the legislative authorities and the general public. Limiting particulate matter in the atmosphere which will result in significant benefits for human health, with associated positive economic consequences. Successful management of particulate matter requires scientific knowledge about particulate matter “from cradle to grave”, covering sources of particles, processes that govern their formation, composition, dispersion and fate in the atmosphere, as well as knowledge about human exposure and associated health and well being. Such knowledge allows to design and perform effective and efficient abatement measures and monitoring. This paper provides an introduction to the research and monitoring regarding particulate matter in Serbia. The contributions were first partly presented at the 2nd international workshop of the WeBIOPATR “Outdoor concentration, size distribution and composition of respirable particles in WB urban area” project in September 2009. This information provides context to the contributions in this number, and was part of the rationale of the project WeBIOPATR.

  13. Physicochemical and oxidative characteristics of semi-volatile components of quasi-ultrafine particles in an urban atmosphere

    Science.gov (United States)

    Verma, Vishal; Pakbin, Payam; Cheung, Ka Lam; Cho, Arthur K.; Schauer, James J.; Shafer, Martin M.; Kleinman, Michael T.; Sioutas, Constantinos

    2011-02-01

    This study examines the physicochemical and redox profiles of atmospheric semi-volatile compounds to evaluate their contribution to the oxidative potential of ambient particulate matter (PM). Concentrated ambient and thermodenuded quasi-ultrafine particles (dithiothreitol) assay. Detailed chemical analyses of PM samples, including organic and elemental carbon, water soluble elements, inorganic ions and PAHs (polycyclic aromatic hydrocarbons), were conducted to quantify the volatility profiles of different PM species, and also to investigate their effect on measured oxidative potential. Refractory constituents, such as metals and elemental carbon, were marginally affected by heating, while labile species such as organic carbon and PAHs showed progressive loss in concentration with increase in TD temperature. The DTT-measured oxidative potential of PM was significantly decreased as the aerosols were heated and their semi-volatile components were progressively removed (42 ± 5%, 47 ± 8% and 66 ± 6% decrease at 50, 100 and 200 °C, respectively). Thus, semi-volatile compounds present in quasi-ultrafine urban aerosols constitute a significant fraction of PM oxidative potential, which is associated with the cellular generation of reactive oxygen species. Regression analysis performed between chemical constituents and DTT activity showed that the oxidative potential was strongly correlated with organic carbon and PAHs ( R ≥ 0.80; p ≤ 0.05).

  14. Composition and sources of organic matter in atmospheric PM 10 over a two year period in Beijing, China

    Science.gov (United States)

    Zhou, Jiabin; Wang, Tieguan; Zhang, Yanping; Zhong, Ningning; Medeiros, Patricia M.; Simoneit, Bernd R. T.

    2009-08-01

    The solvent-extractable organic compounds of atmospheric PM 10 samples, collected over two years beginning in 2003 at urban and suburban sites of Beijing, were characterized using gas chromatography-mass spectrometry (GC-MS). The elemental carbon (EC) contents were determined and ranged from 4.3 to 42 μg m - 3 . Organic compounds in total extracts were identified and included unresolved complex mixture (UCM) and series of n-alkanes, n-alkanols, n-alkanoic acids, polycyclic aromatic hydrocarbons (PAHs); saccharides, alkanedioic acids, steroids, and other biomarkers and source tracers. The seasonal variations of their relative abundances are discussed. The abundance order for the major molecular classes in the particulate organic matter (POM) was the following: UCM > saccharides > n-alkanoic acids > n-alkanes > n-alkanols > PAHs > hydroxy-PAHs > other biomarker tracers. Based on the genetic significance of the molecular tracers, the dominant sources of POM are proposed for the two sampling sites. The emissions from fossil fuel use (both coal and petroleum products), biomass combustion, other pyrolysis sources, higher plant wax, and secondary products contribute > 98.0% of the POM mass. The fossil fuel use (average = 65% of POM) is the largest contributor and derives mainly from vehicular traffic.

  15. Atmospheric sciences annual progress report, 1974

    International Nuclear Information System (INIS)

    Activities in atmospheric sciences in the Department of Applied Science at Brookhaven National Laboratory carried out during 1974 are described. Included are contributions from the Meteorology, Atmospheric Diagnostics, Atmospheric Chemistry Research, and Atmospheric Instrumentation Groups. Programs in Meteorology reported on include diffusion from an off-shore source, plume dynamics studies, modeling of coastal effects on wind and temperature fields and pollutant distributions, effects of indoor shelter on inhalation of airborne radionuclides, chemical-dynamical interactions, techniques for determining acid-rain impact upon the ecology of the eastern U.S., and climatology. Work under Atmospheric Chemistry Research was concentrated on atmospheric aerosol studies, including formation by free radical and neutral association reactions, identification of reactive systems leading to aerosol formation, growth of sodium aerosols under atmospheric conditions and clustering reactions. Atmospheric Diagnostics presents work on field sampling and analytical technology for atmospheric pollutants, airborne sampling systems, atmospheric sulfate particulates methodology, and on a pyroturbidometric method for particulate sulfate discrimination and determination. Methodology for the use of sulfur hexafluoride in field tracer studies is discussed under Atmospheric Instrumentation. A list of publications is included

  16. Partitioning of polycyclic aromatic hydrocarbons, alkylphenols, bisphenol A and phthalates in landfill leachates and stormwater.

    Science.gov (United States)

    Kalmykova, Yuliya; Björklund, Karin; Strömvall, Ann-Margret; Blom, Lena

    2013-03-01

    Partitioning of organic pollutants is essential to their fate, mobility and removal from water and soil. To study the partitioning behavior of selected alkylphenols, bisphenol A, phthalates and polycyclic aromatic hydrocarbons (PAHs), a method for separating the truly dissolved and colloidal phase of organic pollutants was developed, verified and applied to samples of landfill leachate and stormwater from urban areas and waste-sorting sites. Alkylphenols, bisphenol A, phthalates and PAHs were detected in all the untreated samples (total concentrations), most of the filtered samples and frequently in the colloid-bound phase. Concentrations of alkylphenols and PAHs in urban stormwater were one order of magnitude lower than in the landfill leachates and stormwater from waste-sorting sites. The difference between total, dissolved and colloid-bound concentrations in the water samples was not statistically significant for any phenols or phthalates, but for three of the PAHs; naphthalene (mostly dissolved), phenanthrene and fluoranthene (mostly particulate). These results indicate that in landfill leachates and stormwaters, organic pollutants are predominantly attached to colloids and/or truly dissolved in contrast to their expected strong sorption to particulate matter. Occurrence and concentrations of pollutants in dissolved and colloid-bound phases correlated negatively with the K(OW). However, even highly hydrophobic compounds were frequently detected in filtered samples, i.e. the dissolved phases, and it is suggested that the organic content in the colloids decreases the compounds' partition to particles. The results confirm that the K(OW) values of specific organic pollutants well describe the compounds partition-binding process to dissolved organic carbon (DOC) colloids. Our findings call for a re-assessment of the organic pollutants' mobility and associated risks. This knowledge can also serve as a base for selecting efficient treatment methods for stormwater and

  17. Polycyclic aromatic hydrocarbons from rural household biomass burning in a typical Chinese village

    Institute of Scientific and Technical Information of China (English)

    WANG HaiLin; ZHUANG YaHui; HAO ZhengPing; CAO MeiQiu; ZHONG JinXian; WANG XiaoKe; NGUYEN Thi Kim Oanh

    2008-01-01

    Biomass energy sources are still popular in the rural areas of developing countries for cooking and space heating. Since the incomplete combustion of agricultural residues in home-made ranges might lead to both outdoor and indoor air pollution and cause potential health threat to the rural population,we monitored the ambient levels of 16 US EPA priority polycyclic aromatic hydrocarbons (PAHs) at a typical rural site. Ambient particulate PAH samples (PM2.5 and PM10) were taken during both cooking and non-cooking periods. Source emission monitoring was also conducted for both improved and traditional cooking stoves used in the area. Ambient PAHs had a significant increase during the cooking periods and varied from 72.1 to 554.4 ng/m3. The highest total PAH levels were found during the supper cooking time,in which five- and six-ring species accounted for a large proportion. The observed PAH levels during cooking periods at this rural site were even higher than those in urban areas. A good correlation was found between the benzo[a]pyrene level and the total PAH concentration (r=0.98),making benzo[a]pyrene a potential molecular marker for PAH pollution in the rural areas,where biomass burning is typical. The profiles of the particulate PAHs in both ambient air and source emissions showed a high proportion of high molecular-mass PAHs. In addition,emission factors of 16 PAHs from an improved household stove were found to be significantly lower than those from traditional stoves used in China and in other Asian countries.

  18. Polycyclic aromatic hydrocarbons from rural household biomass burning in a typical Chinese village

    Institute of Scientific and Technical Information of China (English)

    NGUYEN; Thi; Kim; Oanh

    2008-01-01

    Biomass energy sources are still popular in the rural areas of developing countries for cooking and space heating. Since the incomplete combustion of agricultural residues in home-made ranges might lead to both outdoor and indoor air pollution and cause potential health threat to the rural population, we monitored the ambient levels of 16 US EPA priority polycyclic aromatic hydrocarbons (PAHs) at a typical rural site. Ambient particulate PAH samples (PM2.5 and PM10) were taken during both cooking and non-cooking periods. Source emission monitoring was also conducted for both improved and tra- ditional cooking stoves used in the area. Ambient PAHs had a significant increase during the cooking periods and varied from 72.1 to 554.4 ng/m3. The highest total PAH levels were found during the supper cooking time, in which five- and six-ring species accounted for a large proportion. The observed PAH levels during cooking periods at this rural site were even higher than those in urban areas. A good correlation was found between the benzo[a]pyrene level and the total PAH concentration (r=0.98), making benzo[a]pyrene a potential molecular marker for PAH pollution in the rural areas, where bio- mass burning is typical. The profiles of the particulate PAHs in both ambient air and source emissions showed a high proportion of high molecular-mass PAHs. In addition, emission factors of 16 PAHs from an improved household stove were found to be significantly lower than those from traditional stoves used in China and in other Asian countries.

  19. Associations of Cough Prevalence with Ambient Polycyclic Aromatic Hydrocarbons, Nitrogen and Sulphur Dioxide: A Longitudinal Study.

    Science.gov (United States)

    Anyenda, Enoch Olando; Higashi, Tomomi; Kambayashi, Yasuhiro; Nguyen, Thao Thi Thu; Michigami, Yoshimasa; Fujimura, Masaki; Hara, Johsuke; Tsujiguchi, Hiromasa; Kitaoka, Masami; Asakura, Hiroki; Hori, Daisuke; Yamada, Yohei; Hayashi, Koichiro; Hayakawa, Kazuichi; Nakamura, Hiroyuki

    2016-01-01

    Information on potential cough triggers including environmental irritants is vital for successful management of chronic cough in patients. We investigated the relationship between ambient levels of particulate polycyclic aromatic hydrocarbons (PAH), nitrogen dioxide (NO₂) and sulphur dioxide (SO₂) exposures with cough prevalence. Eighty-three adult patients, who had been physician diagnosed with at least asthma, cough variant asthma and/or atopic cough, were divided into asthma and non-asthma groups. They recorded daily cough symptoms during 4 January-30 June 2011 study period while daily samples of total suspended particles were simultaneously collected by use of glass fiber filters and the particulate PAH content determined by high performance liquid chromatography coupled with a fluorescence detector. Ambient concentrations of NO₂ and SO₂ were obtained from a local monitoring site. Logistic regression models using generalized estimating equations were used to determine population-averaged estimates of association between cough prevalence and ambient pollutant exposures for the two groups. Fully adjusted odds ratios from single pollutant models were 1.083 (95% confidence interval (CI): 1.029, 1.140) and 1.097 (95% CI: 1.016, 1.185) per 0.57 ng/m³ for lag2 PAH exposure, while only for asthma group had significant associations with NO₂ and SO₂ exposures for both lag2 and lag02. Similar associations were observed in multipollutant models. This finding suggests that ambient PAH, NO₂, and SO₂ exposure even at low levels is related to cough prevalence in adult chronic cough patients and may be considered as aggravating factor during clinical management of the condition. PMID:27517941

  20. Emission characteristics of polycyclic aromatic hydrocarbons from combustion of different residential coals in North China

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Wen X. [Laboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871 (China)], E-mail: wxliu@urban.pku.edu.cn; Dou Han; Wei, Zhi C.; Chang Biao; Qiu, Wei X.; Liu Yuan; Tao Shu [Laboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871 (China)

    2009-02-01

    Emission properties of polycyclic aromatic hydrocarbons (PAHs) from combustion of six residential coals in North China were investigated. The results indicated that, the total emission factors (EFs) for 15 PAH species in gaseous and particulate phases ranged from 52.8 to 1434.8 mg/kg with a decreasing sequence of local bituminous coals and anthracite coals, and honeycomb briquettes were largely dependent on the raw coals used to produce them. Particulate phase, dominated by median or high molecular weight components, made a major contribution (68.8% - 76.5%) to the total EFs for bituminous coals, while gaseous phase with principal low molecular weight species accounted for most (86.3% - 97.9%) of the total EFs for anthracite coals. The phase partitioning of PAH emission for honeycomb briquettes was similarly dependent on the crude coals. The total EFs, phase partitioning and component profiles of emitted PAHs were mainly influenced by the inner components of the studied coals. Burning mode and flue number on household coal-stoves also affected the emission characteristics by means of the oxygen supply. A sum of seven carcinogenic PAHs, benzo(a)pyrene(BaP)-equivalent carcinogenic power and total toxicity potency expressed in 2,3,7,8-tetrachlorodibenzo-dioxin(TCDD) toxic equivalence exhibited that bituminous coals and produced honeycomb briquettes had remarkably elevated values. Fluoranthene, benzo(b)fluoranthene, benzo(k)fluoranthene, chrysene and indeno(1,2,3-cd)pyrene from anthracite coals showed higher levels of BaP-based toxic equivalent factor, though the other toxicity indices were rather low for this type of coal.

  1. Emission characteristics of polycyclic aromatic hydrocarbons from combustion of different residential coals in North China

    International Nuclear Information System (INIS)

    Emission properties of polycyclic aromatic hydrocarbons (PAHs) from combustion of six residential coals in North China were investigated. The results indicated that, the total emission factors (EFs) for 15 PAH species in gaseous and particulate phases ranged from 52.8 to 1434.8 mg/kg with a decreasing sequence of local bituminous coals and anthracite coals, and honeycomb briquettes were largely dependent on the raw coals used to produce them. Particulate phase, dominated by median or high molecular weight components, made a major contribution (68.8% - 76.5%) to the total EFs for bituminous coals, while gaseous phase with principal low molecular weight species accounted for most (86.3% - 97.9%) of the total EFs for anthracite coals. The phase partitioning of PAH emission for honeycomb briquettes was similarly dependent on the crude coals. The total EFs, phase partitioning and component profiles of emitted PAHs were mainly influenced by the inner components of the studied coals. Burning mode and flue number on household coal-stoves also affected the emission characteristics by means of the oxygen supply. A sum of seven carcinogenic PAHs, benzo(a)pyrene(BaP)-equivalent carcinogenic power and total toxicity potency expressed in 2,3,7,8-tetrachlorodibenzo-dioxin(TCDD) toxic equivalence exhibited that bituminous coals and produced honeycomb briquettes had remarkably elevated values. Fluoranthene, benzo(b)fluoranthene, benzo(k)fluoranthene, chrysene and indeno(1,2,3-cd)pyrene from anthracite coals showed higher levels of BaP-based toxic equivalent factor, though the other toxicity indices were rather low for this type of coal

  2. Polycyclic aromatic hydrocarbons, polychlorinated biphenyls and organochlorine pesticides in urban air of Konya, Turkey

    Science.gov (United States)

    Ozcan, Senar; Aydin, Mehmet Emin

    2009-08-01

    Polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) were determined in urban air samples of Konya, Turkey between August 2006 and May 2007. The concentrations of pollutants in both the gas and particulate phase were separately analysed. The average total (gas + particulate) concentrations of PAHs, PCBs and OCPs were determined as 206 ng m - 3 , 0.106 ng m - 3 , 4.78 ng m - 3 respectively. All of the investigated target compounds were dominantly found in the gas phase except OCPs. Higher air concentrations of PAHs were found at winter season while the highest concentrations of PCBs were determined in September. The highest OCPs were detected in October and in March. In urban air of Konya, PCB 28 and PCB 52 congeners represent 46% and 35% of total PCBs while Phenanthrene, Fluoranthene, Pyrene accounted for 29%, 13%, 10% of total PAHs. HCH compounds (α + β + γ + δ-HCH), total DDTs ( p, p'-DDE, p, p'-DDD, p, p'-DDT), Endosulfan compounds (Endosulfan I, Endosulfan II, Endosulfan sulfate) were dominantly determined as 30%, 21%, 20% of total OCPs respectively. Considering the relation between these compounds with temperature, there was no significant correlation observed. Despite banned/restricted use in Turkey, some OCPs were determined in urban air. These results demonstrated that they are either illegally being used in the course of agricultural activity and gardens in Konya or they are residues of past use in environment. According to these results, it can be suggested that Konya is an actively contributing region to persistent organic pollutants in Turkey.

  3. Large-eddy simulation and Lagrangian stochastic modelling of solid particle and droplet dispersion and mixing. Application to atmospheric pollution; Dispersion et melange turbulents de particules solides et de gouttelettes par une simulation des grandes echelles et une modelisation stochastique lagrangienne. Application a la pollution de l'atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Vinkovic, I.

    2005-07-15

    In order to study atmospheric pollution and the dispersion of industrial stack emissions, a large eddy simulation with the dynamic Smagorinsky-Germano sub-grid-scale model is coupled with Lagrangian tracking of fluid particles containing scalar, solid particles and droplets. The movement of fluid particles at a sub-grid level is given by a three-dimensional Langevin model. The stochastic model is written in terms of sub-grid-scale statistics at a mesh level. By introducing a diffusion model, the coupling between the large-eddy simulation and the modified three-dimensional Langevin model is applied to passive scalar dispersion. The results are validated by comparison with the wind-tunnel experiments of Fackrell and Robins (1982). The equation of motion of a small rigid sphere in a turbulent flow is introduced. Solid particles and droplets are tracked in a Lagrangian way. The velocity of solid particles and droplets is considered to have a large scale component (directly computed by the large-eddy simulation) and a sub-grid scale part. Because of inertia and gravity effects, solid particles and droplets, deviate from the trajectories of the surrounding fluid particles. Therefore, a modified Lagrangian correlation timescale is introduced into the Langevin model previously developed for the sub-grid velocity of fluid particles. Two-way coupling and collisions are taken into account. The results of the large-eddy simulation with solid particles are compared with the wind-tunnel experiments of Nalpanis et al. (1993) and of Taniere et al. (1997) on sand particles in saltation and in modified saltation, respectively. A model for droplet coalescence and breakup is implemented which allows to predict droplet interactions under turbulent flow conditions in the frame of the Euler/Lagrange approach. Coalescence and breakup are considered as a stochastic process with simple scaling symmetry assumption for the droplet radius, initially proposed by Kolmogorov (1941). At high

  4. Emissivity of rocket plume particulates.

    OpenAIRE

    Whisman, Curtis D.

    1992-01-01

    The optical properties of motor aluminum oxide are required inputs to current plume signature prediction codes, such as SIRRM. Accurate predictions are possible only if variations in the particle emissivity due to changes in particle size, contamination, and changing temperature, etc. , are known . This investigation demonstrated a simplified method for determination of the emissivity of rocket motor generated alumina. Plume particulate material was collected on ...

  5. Composition of Indoor Particulate Matter

    Czech Academy of Sciences Publication Activity Database

    Smolík, Jiří; Schwarz, Jaroslav; Dohányosová, Pavla

    -: -, 2006 - (Fernandes, D.), s. 283-286. (Indoor Climate. II). [Healthy Buildings 2006. Lisboa (PT), 04.06.2006-08.06.2006] R&D Projects: GA ČR(CZ) GA101/04/1190; GA ČR(CZ) GA205/03/1560 Institutional research plan: CEZ:AV0Z40720504 Keywords : indoor particulate matter * chemical composition Subject RIV: CF - Physical ; Theoretical Chemistry

  6. 75 FR 8937 - Development of a Relative Potency Factor (RPF) Approach for Polycyclic Aromatic Hydrocarbon (PAH...

    Science.gov (United States)

    2010-02-26

    ... AGENCY Development of a Relative Potency Factor (RPF) Approach for Polycyclic Aromatic Hydrocarbon (PAH...) Approach for Polycyclic Aromatic Hydrocarbon (PAH) Mixtures'' (EPA/635/R-08/012A). The draft document was... of a Relative Potency Factor (RPF) Approach for Polycyclic Aromatic Hydrocarbon (PAH) Mixtures''...

  7. Composition of semi-volatile organic compounds in the urban atmosphere of Singapore: influence of biomass burning

    Science.gov (United States)

    He, J.; Zielinska, B.; Balasubramanian, R.

    2010-12-01

    An intensive field study was conducted in the urban atmosphere of Singapore to investigate the composition of organic compounds in both gaseous and particulate phases during the period of August to early November 2006. 17 atmospheric samples were collected. These samples were subjected to accelerated solvent extraction with a mixture of dichloromethane and acetone and separated into functional group fractions for analyses by GC/MS. Over 180 organic compounds belonging to three major fractions (n-alkanes, polycyclic aromatic hydrocarbons - PAHs, and polar organic compounds - POCs) were identified and quantified. The characteristics and abundance of the n-alkanes, PAHs, mono and dicarboxylic acids, methoxylated phenols and other POCs were determined. The composition of these organic compounds fluctuated temporally with most of them being relatively higher in October than those in other months of the sampling period. 3-D backward air mass trajectory analyses together with the carbon preference index (CPI), molecular diagnostic ratios and molecular markers were used to investigate the origin of organic species measured in this study. Based on these diagnostic tools, the increased abundance of atmospheric organic species during October could be attributed to the occurrence of regional smoke haze episodes due to biomass burning in Indonesia. Among the POCs investigated, phthalic acid and cis-pinonic acid were abundant during October 2006. These two acids showed strong linear relationships with maximum daily ozone concentrations throughout the entire sampling period. This correlation with ozone suggested that the secondary aerosol constituents such as phthalic and cis-pinonic acids were probably formed through O3-induced photochemical transformation.

  8. Relative Influence of Trans-Pacific and Regional Atmospheric Transport of PAHs in the Pacific Northwest, U.S.

    Science.gov (United States)

    Lafontaine, Scott; Schrlau, Jill; Butler, Jack; Jia, Yuling; Harper, Barbara; Harris, Stuart; Bramer, Lisa M; Waters, Katrina M; Harding, Anna; Simonich, Staci L Massey

    2015-12-01

    The relative influences of trans-Pacific and regional atmospheric transport on measured concentrations of polycyclic aromatic hydrocarbons (PAHs), PAH derivatives (nitro- (NPAH) and oxy-(OPAH)), organic carbon (OC), and particulate matter (PM) less than 2.5 μm in diameter (PM2.5) were investigated in the Pacific Northwest, U.S. in 2010-2011. Ambient high volume PM2.5 air samples were collected at two sites in the Pacific Northwest: (1.) Mount Bachelor Observatory (MBO) in the Oregon Cascade Range (2763 m above sea level (asl)) and 2.) Confederated Tribes of the Umatilla Indian Reservation (CTUIR) in the Columbia River Gorge (CRG) (954 m asl). At MBO, the 1,8-dinitropyrene concentration was significantly positively correlated with the time a sampled air mass spent over Asia, suggesting that this NPAH may be a good marker for trans-Pacific atmospheric transport. At CTUIR, NOx, CO2, and SO2 emissions from a 585 MW coal fired power plant, in Boardman OR, were found to be significantly positively correlated with PAH, OPAH, NPAH, OC, and PM2.5 concentrations. By comparing the Boardman Plant operational time frames when the plant was operating to when it was shut down, the plant was found to contribute a large percentage of the measured PAH (67%), NPAH (91%), OPAH (54%), PM2.5 (39%), and OC (38%) concentrations at CTUIR and the CRG prior to Spring 2011 and likely masked trans-Pacific atmospheric transport events to the CRG. Upgrades installed to the Boardman Plant in the spring of 2011 dramatically reduced the plant's contribution to PAH and OPAH concentrations (by ∼72% and ∼40%, respectively) at CTUIR and the CRG, but not NPAH, PM2.5 or OC concentrations. PMID:26151337

  9. Instrumental neutron activation analysis data for cloud-water particulate samples, Mount Bamboo, Taiwan

    Science.gov (United States)

    Lin, Neng-Huei; Sheu, Guey-Rong; Wetherbee, Gregory A.; Debey, Timothy M.

    2013-01-01

    Cloud water was sampled on Mount Bamboo in northern Taiwan during March 22-24, 2002. Cloud-water samples were filtered using 0.45-micron filters to remove particulate material from the water samples. Filtered particulates were analyzed by instrumental neutron activation analysis (INAA) at the U.S. Geological Survey National Reactor Facility in Denver, Colorado, in February 2012. INAA elemental composition data for the particulate materials are presented. These data complement analyses of the aqueous portion of the cloud-water samples, which were performed earlier by the Department of Atmospheric Sciences, National Central University, Taiwan. The data are intended for evaluation of atmospheric transport processes and air-pollution sources in Southeast Asia.

  10. Partition of polycyclic aromatic hydrocarbons on organobentonites

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    A series of organobentonites synthesized by exchanging organiccation such as dodecyltri-methylammonium (DTMA),benzyldimethyltetradecylammonium (BDTDA), cetyltrimethyl-ammonium (CTMA), octodeyltrimethylammonium (OTMA) on bentonite. The optimal condition, properties and mechanisms for the organobentonites to sorb phenanthrene, anthracene, naphthalene, acenaphthene in water were investigated in detail. The partition behavior was determined for four polycyclic aromatic hydrocarbons (PAHs), such as naphthalene, phenanthrene, anthracene and acenaphthene, from water to a series of organobentonites. The interlayer spacings and organic carbon contents of organobentonites, removal rate and sorption capacities for organobentonites to treat phenanthrene,anthracene, naphthalene, acenaphthene were correlated to the length of alkyl chains and the amounts of cation surfactant exchanged on Foundation item: the bentonite. Phenanthrene, anthracene, naphthalene, and acenaphthene sorption to organobentonites were characterized by linear isotherms, indicating solute partition between water and the organic phase composed of the large alkyl functional groups of quaternary ammonium cations. PAHs distribution coefficients (Kd)between organobentonites and water were proportional to the organic carbon contents of organobentonites. However, the partition coefficients (Koc) were nearly constants for PAHs in the system of organobentonite-water. The Koc of phenanthrene, anthracene,naphthalene, acenaphthene were 2.621x105, 2.106x105, 2.247x104,5.085x104, respectively. The means Koc values on the organobentonites are about ten to twenty times larger than the values on the soils/sediments, what is significant prerequisite for organobentonite to apply to remediation of pollution soil and groundwater. The sorption mechanism was also evaluated from octanol-water partition coefficients and aqueous solubility of PAHs. The correlations between lgKoc and 1gkow, 1gKoc and 1gS for PAHs in the system of water

  11. Environmental Remediation: Removal of polycyclic aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Nkansah, Marian Asantewah

    2012-11-15

    Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous persistent semi-volatile organic compounds. They are contaminants that are resistant to degradation and can remain in the environment for long periods due to their high degree of conjugation, and aromaticity. PAHs are present in industrial effluents as products of incomplete combustion processes of organic compounds. Petroleum, coal and shale oil contain extremely complex mixtures of these PAHs, and their transport and refining process can also result in the release of PAHs. It is therefore prudent that such effluents are treated before discharge into the environment. In this project, different approaches to the treatment of PAHs have been investigated. Hydrous pyrolysis has been explored as a potential technique for degrading PAHs in water using anthracene as a model compound. The experiments were performed under different conditions of temperature, substrate, redox systems and durations. The conditions include oxidising systems comprising pure water, hydrogen peroxide and Nafion-SiO2 solid catalyst in water; and reducing systems of formic acid and formic acid / Nafion-SiO2 / Pd-C catalysts to assess a range of reactivities. Products observed in GCMS analysis of the extract from the water phase include anthrone, anthraquinone, xanthone and multiple hydro-anthracene derivatives (Paper I). In addition a modified version of the Nafion-SiO2 solid catalyst in water oxidising system was tested; and reducing systems of formic acid and formic acid / Nafion-SiO2 / Pd-C catalysts were adopted for the conversion of a mixture of anthracene, fluorene and fluoranthene. The rate of conversion in the mixture was high as compared to that of only anthracene (Paper II). Also the use of LECA (Lightweight expanded clay aggregates) as an adsorbent (Paper III) for PAHs (phenanthrene, fluoranthene and pyrene) removal from water has been.(Author)

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

    International Nuclear Information System (INIS)

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

  13. Polycyclic aromatic hydrocarbon composition in soils and sediments of high altitude lakes

    Energy Technology Data Exchange (ETDEWEB)

    Grimalt, Joan O.; Drooge, Barend L. van; Ribes, Alejandra; Fernandez, Pilar; Appleby, Peter

    2004-09-01

    Polycyclic aromatic hydrocarbons (PAH) in lake sediments and nearby soils of two European high mountain regions, Pyrenees and Tatra, have been studied. Similar mixtures of parent PAH were observed in all cases, indicating predominance of airborne transported combustion products. Nevertheless, the composition of these atmospherically long-range transported PAH was better preserved in the superficial layers of soils than sediments. This difference points to significant PAH degradation process, e.g. during lake water column transport, before accumulation in the latter. Post-depositional transformation was also different in both types of environmental compartments. Thus, lake sediments exhibit higher preservation of the more labile PAH involving lower degree of post-depositional oxidation. However, they also show the formation of major amounts of perylene by diagenetic transformation in the deep sections. This compound is not formed in soils where downcore enrichments of phenanthrene are observed, probably as a consequence of diagenetic aromatization of diterpenoids.

  14. Measurement of gas-phase polycyclic aromatic hydrocarbons (PAH) in gasoline vehicle exhaust

    International Nuclear Information System (INIS)

    Polycyclic aromatic hydrocarbons (PAH) are emitted at low levels from most combustion sources including motor vehicles. Extensive studies have been carried out in the past on the identification and quantitation of PAH in particular matter, primarily from diesel vehicles; however, only limited data are available on gas phase emissions from motor vehicles. Gas phase emissions are important from both a health perspective and because of their higher chemical reactivity during atmospheric transport. A method was sought to allow the authors to measure gas phase PAH in diluted vehicle exhaust over the relatively short collection times permitted during the U. S. Environmental Protection Agency (EPA) Urban Dynamometer Driving Schedule (UDDS) or Federal Test Procedure (FTP). In this paper, the authors describe their results on the development of a method using adsorption/thermal desorption with Tenax solid absorbent for the analysis of PAH and PAH derivatives in dilute vehicle exhaust

  15. City air pollution of polycyclic aromatic hydrocarbons and other mutagens: occurrence, sources and health effects

    DEFF Research Database (Denmark)

    Nielsen, T.; Ejsing Jørgensen, Hans; Larsen, J.C.;

    1996-01-01

    The presence of polycyclic aromatic hydrocarbons (PAH), mutagens and other air pollutants was investigated in a busy street in central Copenhagen and in a park area adjacent to the street. The winter concentration of benzo(a)pyrene was 4.4+/-1.2 ng/m(3) in the street air and 1.4+/-0.6 ng/m(3) in...... the city park. The atmospheric concentrations of PAH decreased in the order of: street > city background air similar to suburbs > village > open land. The traffic contribution of PAH to street air was estimated to be 90% on working days and 60% during weekends and its contribution to city background...... air was estimated to be 40%. Four different approaches to evaluate the health effects are discussed. The direct effect of PAH air pollution, and other mutagens, is considered to be a maximum of five lung cancer cases each year out of one million people....

  16. Polycyclic aromatic hydrocarbons alter the structure of oceanic and oligotrophic microbial food webs

    KAUST Repository

    Cerezo, Maria Isabel

    2015-11-01

    One way organic pollutants reach remote oceanic regions is by atmospheric transport. During the Malaspina-2010 expedition, across the Atlantic, Indian, and Pacific Oceans, we analyzed the polycyclic aromatic hydrocarbon (PAH) effects on oceanic microbial food webs. We performed perturbation experiments adding PAHs to classic dilution experiments. The phytoplankton growth rates were reduced by more than 5 times, being Prochlorococcus spp. the most affected. 62% of the experiments showed a reduction in the grazing rates due to the presence of PAHs. For the remaining experiments, grazing usually increased likely due to cascading effects. We identified changes in the slope of the relation between the growth rate and the dilution fraction induced by the pollutants, moving from no grazing to V-shape, or to negative slope, indicative of grazing increase by cascade effects and alterations of the grazers\\' activity structure. Our perturbation experiments indicate that PAHs could influence the structure oceanic food-webs structure.

  17. Determining produced water originating polycyclic aromatic hydrocarbons in North Sea waters: comparison of sampling techniques

    International Nuclear Information System (INIS)

    A field study was carried out in the Norwegian sector of the North Sea during May and June 1997. The purpose was to measure the concentration of produced water originating polycyclic aromatic hydrocarbons (PAH) in seawater and to compare different sampling techniques for use in future monitoring programs. Three methods were used for direct water sampling: (1) in situ large volume sampling of particulate and dissolved hydrocarbons onto filters and XAD resins, (2) solid phase extraction (SPE) using polystyrene-divinylbenzene disks, (3) whole bulk water sampling. In addition, sampling by semi-permeable membrane devices (SPMDs) and blue mussels (Mytilus edulis) was used to obtain a 4 weeks average of the concentration of the target compounds in seawater. The samples were processed and analysed by GC-MS for determination of PAH concentrations. The measured concentrations were generally found to be low, and in many cases below the limits of detection. The comparison of sampling techniques showed that blue mussels and SPMDs are suitable for measuring PAH in both near-and far-field seawater. In situ large volume water sampling was also suitable for a wide range of PAH concentrations, but this technique was limited by high break-through of the low-molecular weight compounds, such as naphthalenes. The small sampling volumes limited the SPE and whole water sampling techniques, resulting in potential detection limit problems These grab-sampling techniques may, however, be suitable for monitoring in the near-field areas around the platforms. (Author)

  18. Biomonitoring of polycyclic aromatic hydrocarbons from coke oven emissions and reproductive toxicity in nonsmoking workers.

    Science.gov (United States)

    Jeng, Hueiwang Anna; Pan, Chih-Hong; Lin, Wen-Yi; Wu, Ming-Tsang; Taylor, Steven; Chang-Chien, Guo-Ping; Zhou, Guodong; Diawara, Norou

    2013-01-15

    The objective of the cross-sectional study was to assess whether exposure to polycyclic aromatic hydrocarbons (PAHs) from coke oven emissions contributed to alteration of semen quality and sperm DNA integrity in nonsmoking workers. Nonsmoking coke oven workers from a steel plant in Taiwan served as the exposure groups (topside-oven workers for the high exposure group and side-oven workers for the low exposure group), and administrators and security personnel in the plant served as the control. An exposure assessment was conducted to determine both particulate and gaseous phase of PAH levels and urinary 1-hydroxypyrene (1-OHP) levels. Semen quality was analyzed according to WHO guidelines. DNA fragmentation and bulky DNA adducts were measured to assess sperm DNA integrity. There was no significant difference in sperm concentrations, vitality, and DNA fragmentation between the exposed group and the control. The high exposure group experienced significantly lower percentages of normal morphology as compared with the control (p=0.0001). Bulky DNA adducts were detected in the exposed group that were significant higher than the control (p=0.04). Exposure to PAHs from coke-oven emissions could contribute to increased levels of bulky DNA adducts in sperm. PMID:23314003

  19. NATO Advanced Research and CNRS Workshop on Polycyclic Aromatic Hydrocarbons and Astrophysics

    CERN Document Server

    d’Hendecourt, L; Boccara, N

    1987-01-01

    The near Infra-Red emission of the Interstellar Medium is a very puzzling subject. In the brightest regions, where spectroscopic observa­ tions are possible from the ground, several bands (3.3 - 3.4 - 6.2 - 7.7 - 8.6 - 11.3 ~m) have been observed since 1973. The absence of satisfying explanation was so obvious that they were called "Unidenti­ fied IR Emission Bands". The puzzle still increased when were known the first results of the general IR sky survey made by the satellite IRAS. On a large scale, the near IR emission of the Interstellar medium was expected to be very small but it was observed to be about one third of the total IR emission for our own galaxy ..• The situation has moved in 1984 when it was suggested that a class of stable organic molecules, the Polycyclic Aromatic Hydrocarbons (PAH's) could be at the origin of this near IR emission. Initially based on the required refractory character of particules that should be heated to high temperature without subliming, this hypothesis leads to a s...

  20. Identification of products formed during the heterogeneous nitration and ozonation of polycyclic aromatic hydrocarbons

    Science.gov (United States)

    Cochran, Richard E.; Jeong, Haewoo; Haddadi, Shokouh; Fisseha Derseh, Rebeka; Gowan, Alexandra; Beránek, Josef; Kubátová, Alena

    2016-03-01

    The 3- and 4-ring polycyclic aromatic hydrocarbons (PAHs) are the most abundant of PAHs in air particulate matter (PM). Thus we have investigated heterogeneous oxidation of 3- and 4-ring PAHs in a small-scale flow reactor using quartz filter as a support. Four representative PAHs, anthracene, phenanthrene, pyrene, and fluoranthene, were exposed to either NO2, O3 or NO2+O3 (NO3/N2O5) with a goal to identify and attempt quantification of major product distribution. A combination of gas chromatography with mass spectrometry (GC-MS) with/without derivatization and liquid chromatography with high resolution MS (LC-HRMS) was used for identification. For the first time, a comprehensive characterization of a broad range of products enabled identifying ketone/diketone, aldehyde, hydroxyl, and carboxylic acid PAH derivatives. Exposure to NO3/N2O5 (formed by reacting NO2 with O3, a more powerful reactant than either O3 or NO2) produced additional compounds not observed with either oxidant alone. Multiple isomers of nitrofluoranthene and, for the first time, nitrophenanthrene were identified. In addition hydroxy-nitro-PAH derivatives were observed for the reaction of anthracene with NO3/N2O5. Monitoring of specific common ions such as those of 176 and 205 m/z attributed to carbonyl phenanthrene and deprotonated phenanthrene ions respectively was shown to be a useful tool for identification of multiple pyrene oxidation products.

  1. Detection and identification of OH-NO2-aromatic/polycyclic compounds

    International Nuclear Information System (INIS)

    The authors recent studies indicate that a wide variety of OH-NO2-substituted aromatic compounds exist in ambient air and source emissions. Those classes which have been positively and tentatively identified on the basis of mass spectra include OH-NO2-substituted aromatic, ketone, O-heterocycle, and N-heterocycle. Levels of OH-NO2-benzene, toluene, naphthalene isomers (OH-NO2-AR) were measured in ambient air at levels equal to or greater than the levels of the corresponding NO2-aromatics (NO2-AR). For selected ambient air samples in which filter and XAD-2 extracts were analyzed separately for OH-NO2-AR, they observed results that are consistent with the phase distribution theory of Arey and Atkinson for NO2-AR: photochemical products appear predominantly in the vapor phase (XAD-2) and source emissions appear predominantly in the particle phase. The ortho-substituted OH-NO2-AR, which were found almost exclusively in the XAD-2 extract, appear to be photochemical products while para-substituted OH-NO2-AR, found in both XAD-2 and filter extracts, may be both photochemical products and source emissions. Source emissions may be those para-substituted OH-NO2-AR of the filter extract. The diverse OH-NO2-polycyclic compounds listed above were detected in the particulate extract of ambient air impacted by various coal combustion industries. Therefore, the finding of substituted N-heterocyclic compounds may not be unexpected

  2. Particulate silica and Si recycling in the surface waters of the Eastern Equatorial Pacific

    DEFF Research Database (Denmark)

    Adjou, Mohamed; Tréguer, Paul; Dumousseaud, Cynthia;

    2011-01-01

    SiO2) was generally <10 nmol Si l-1 with maximum concentrations reaching 25 nmol l-1 in surface waters. These low concentrations confirm low atmospheric inputs of particulate Si, consistent with reported low inputs of wind-borne material in the EEP. In spite of active upwelling of silicic acid...

  3. Fission product transport in the atmosphere

    International Nuclear Information System (INIS)

    In the present thesis,a theoretical treatment has been developed for investigating the fission product transport in the atmosphere, and expressing its underlying dynamics. Some basic material has been critically reviewed for the purpose of establishing the mathematical equations that govern the motion of a general pollutant - whether it is radioactive or not - in the atmosphere. Such review included the study of particulate matter motion in the atmosphere and radioactive cloud motion, together with the analysis of available mathematical models for atmospheric dispersion

  4. Qualitative and quantitative determination of water in airborne particulate matter

    OpenAIRE

    Canepari, S.; C. Farao; E. Marconi; C. Giovannelli; C. Perrino

    2013-01-01

    This paper describes the optimization and validation of a new simple method for the quantitative determination of water in atmospheric particulate matter (PM). The analyses are performed by using a coulometric Karl-Fisher system equipped with a controlled heating device; different water contributions are separated by the application of an optimized thermal ramp (three heating steps: 50–120 °C, 120–180 °C, 180–250 °C).

    The analytical performance of the method was verified ...

  5. Comparison of Particulate Mercury Measured with Manual and Automated Methods

    Directory of Open Access Journals (Sweden)

    Rachel Russo

    2011-01-01

    Full Text Available A study was conducted to compare measuring particulate mercury (HgP with the manual filter method and the automated Tekran system. Simultaneous measurements were conducted with the Tekran and Teflon filter methodologies in the marine and coastal continental atmospheres. Overall, the filter HgP values were on the average 21% higher than the Tekran HgP, and >85% of the data were outside of ±25% region surrounding the 1:1 line. In some cases the filter values were as much as 3-fold greater, with

  6. Characterization of chemical components and bioreactivity of fine particulate matter (PM2.5) during incense burning.

    Science.gov (United States)

    Lui, K H; Bandowe, Benjamin A Musa; Ho, Steven Sai Hang; Chuang, Hsiao-Chi; Cao, Jun-Ji; Chuang, Kai-Jen; Lee, S C; Hu, Di; Ho, K F

    2016-06-01

    The chemical and bioreactivity properties of fine particulate matter (PM2.5) emitted during controlled burning of different brands of incense were characterized. Incenses marketed as being environmentally friendly emitted lower mass of PM2.5 particulates than did traditional incenses. However, the environmentally friendly incenses produced higher total concentrations of non-volatile polycyclic aromatic hydrocarbons (PAHs) and some oxygenated polycyclic aromatic hydrocarbons (OPAHs). Human alveolar epithelial A549 cells were exposed to the collected PM2.5, followed by determining oxidative stress and inflammation. There was moderate to strong positive correlation (R > 0.60, p < 0.05) between selected PAHs and OPAHs against oxidative-inflammatory responses. Strong positive correlation was observed between interleukin 6 (IL-6) and summation of total Group B2 PAHs/OPAHs (∑7PAHs/ΣOPAHs). The experimental data indicate that emissions from the environmentally friendly incenses contained higher concentrations of several PAH and OPAH compounds than did traditional incense. Moreover, these PAHs and OPAHs were strongly correlated with inflammatory responses. The findings suggest a need to revise existing regulation of such products. PMID:26994327

  7. Quantification of PAHs and oxy-PAHs on airborne particulate matter in Chiang Mai, Thailand, using gas chromatography high resolution mass spectrometry

    Science.gov (United States)

    Walgraeve, Christophe; Chantara, Somporn; Sopajaree, Khajornsak; De Wispelaere, Patrick; Demeestere, Kristof; Van Langenhove, Herman

    2015-04-01

    An analytical method using gas chromatography high resolution mass spectrometry was developed for the determination of 16 polycyclic aromatic hydrocarbons (PAHs) and 12 oxygenated PAHs (of which 4 diketones, 3 ketones, 4 aldehydes and one anhydride) on atmospheric particulate matter with an aerodynamic diameter less than 10 μm (PM10). The magnetic sector mass spectrometer was run in multiple ion detection mode (MID) with a mass resolution above 10 000 (10% valley definition) and allows for a selective accurate mass detection of the characteristic ions of the target analytes. Instrumental detection limits between 0.04 pg and 1.34 pg were obtained for the PAHs, whereas for the oxy-PAHs they ranged between 0.08 pg and 2.13 pg. Pressurized liquid extraction using dichloromethane was evaluated and excellent recoveries ranging between 87% and 98% for the PAHs and between 74% and 110% for 10 oxy-PAHs were obtained, when the optimum extraction temperature of 150 °C was applied. The developed method was finally used to determine PAHs and oxy-PAHs concentration levels from particulate matter samples collected in the wet season at 4 different locations in Chiang Mai, Thailand (n = 72). This study brings forward the first concentration levels of oxy-PAHs in Thailand. The median of the sum of the PAHs and oxy-PAHs concentrations was 3.4 ng/m3 and 1.1 ng/m3 respectively, which shows the importance of the group of the oxy-PAHs as PM10 constituents. High molecular weight PAHs contributed the most to the ∑PAHs. For example, benzo[ghi]perylene was responsible for 30-44% of the ∑PAHs. The highest contribution to ∑oxy-PAHs came from 1,8-napthalic anhydride (26-78%), followed by anthracene-9,10-dione (4-27%) and 7H-benzo[de]anthracene-7-one (6-26%). Indications of the degradation of PAHs and/or formation of oxy-PAHs were observed.

  8. Characterisation and quantification of trace metal elements in atmospheric deposition and particularities in the Aspe valley (Pyrenees): implementation of road traffic air quality indicators; Caracterisation et quantification des elements traces metalliques dans les depots et les particules atmospheriques de la vallee d'Aspe (Pyrenees): Mise en place d'indicateurs de la qualite de l'air lies au trafic routier

    Energy Technology Data Exchange (ETDEWEB)

    Veschambre, S

    2006-04-15

    This study of inputs of trace metal elements (TME) in the Aspe valley (Pyrenees Atlantiques) has two objectives: (1) to define a reference state of metallic contaminants for the monitoring of road traffic emissions since the opening of the Somport tunnel and, (2) to evaluate sources and climatic conditions which contribute to TME inputs in the Aspe valley. To establish air quality indicators, TME (Al, Na, Mg, K, V, Mn, Cr, Zn, Cu, Rb, Cd, Sn, Sb, Ba, Ce, Pb and U) and lead isotopic ratios ({sup 208}Pb/{sup 206}Pb, {sup 206}Pb/{sup 207}Pb and {sup 208}Pb/{sup 207}Pb) were determined in the atmospheric receptors (fresh snow, wet deposition, atmospheric particulates and lichen). Sampling and analyses with ultra clean procedures were employed for TME quantification. Variability of atmospheric receptors studied, allows integration on a daily and pluri-annual temporal scale and a spatial scale in the North-South axis of the valley and as a function of the altitude from the road. The Aspe valley presents a level of contamination characteristic of remote European areas and the metallic contaminants identified are Cd, Sb, Zn, Cu, Pb and Sn. In the low valley, air quality indicators indicate contaminant contributions (i) from local emissions of domestic heat sources, from agricultural burning practices and road traffic, and (ii) from regional anthropogenic sources of waste incinerators, metallurgic industries and urban centres. In altitude, the valley is significantly influenced by wind erosion and long range transport of TME in the Northern Hemisphere. Characterisation of TME and the isotopic ratios of Pb in the Somport tunnel indicate (i) a significant emission of Cu, Sb, Zn and Ba and (ii) an isotopic composition from a slightly radiogenic source even though Pb concentrations indicate low emissions from road traffic emissions. Nevertheless, the low traffic volume in the Aspe valley prevents conclusive evidence of significant contamination from road traffic. (author)

  9. Evaluation of principal cannabinoids in airborne particulates

    Energy Technology Data Exchange (ETDEWEB)

    Balducci, C., E-mail: balducci@iia.cnr.it [Italian National Research Council, Institute for Atmospheric Pollution (CNR-IIA), Monterotondo Stazione (Italy); Nervegna, G.; Cecinato, A. [Italian National Research Council, Institute for Atmospheric Pollution (CNR-IIA), Monterotondo Stazione (Italy)

    2009-05-08

    The determination of delta(9)-tetrahydrocannabinol ({Delta}{sup 9}-THC), cannabidiol (CND) and cannabinol (CNB), primary active components in cannabis preparation, was carried out on airborne particulates by applying a specific procedure consisting of soot extraction by ultrasonic bath, purification by solvent partitioning, derivatization with N-(t-butyldimethylsilyl)-N-methyl-trifluoroacetamide, and separation/detection through gas chromatography coupled with tandem mass spectrometry. The optimized procedure was found suitable for measuring the three psychotropic substances at concentrations ranging from ca. 0.001 to ca. 5.0 ng cm{sup -3} of air, with recoveries always higher than 82%, accuracy >7.3% and precision >90%. Application of the procedure performed on field in Rome and Bari, Italy, demonstrated that all three compounds contaminate the air in Italian cities whereas in Algiers, Algeria, only cannabinol, the most stable in the atmosphere, exceeded the limit of quantification of the method. The relative percentages of the three cannabinoids in general reproduced those typical of the Cannabis sativa plant and were very different from those found in human blood, urine and sweat.

  10. Evaluation of principal cannabinoids in airborne particulates

    International Nuclear Information System (INIS)

    The determination of delta(9)-tetrahydrocannabinol (Δ9-THC), cannabidiol (CND) and cannabinol (CNB), primary active components in cannabis preparation, was carried out on airborne particulates by applying a specific procedure consisting of soot extraction by ultrasonic bath, purification by solvent partitioning, derivatization with N-(t-butyldimethylsilyl)-N-methyl-trifluoroacetamide, and separation/detection through gas chromatography coupled with tandem mass spectrometry. The optimized procedure was found suitable for measuring the three psychotropic substances at concentrations ranging from ca. 0.001 to ca. 5.0 ng cm-3 of air, with recoveries always higher than 82%, accuracy >7.3% and precision >90%. Application of the procedure performed on field in Rome and Bari, Italy, demonstrated that all three compounds contaminate the air in Italian cities whereas in Algiers, Algeria, only cannabinol, the most stable in the atmosphere, exceeded the limit of quantification of the method. The relative percentages of the three cannabinoids in general reproduced those typical of the Cannabis sativa plant and were very different from those found in human blood, urine and sweat.

  11. Spatial distribution characteristics of polycyclic musks as a chemical marker in river water and sediment compared with other typical pollutants.

    Science.gov (United States)

    Mu, Li; Wen, Jianping

    2013-01-01

    Polycyclic musks (PMs), widely used in the cosmetic and perfume industries, are gaining attention as a new type of persistent organic pollutant (POP). The related contamination in developing countries, such as China, where the use of these compounds is increasing, needs to be closely monitored. This work systematically studied the distribution profile (water-suspended particulate-sediment-porewater) of PMs in Haihe River, China. The average concentrations of PMs were comparable to those of the traditional POPs. The typical PMs (galaxolide and tonalide) exhibited different environmental behaviors in various media. Water played a more significant role than suspended particulates in the transport of pollutants. Importantly, this work explored the relationships among PMs, surfactant, phosphorus, carbon, salinity, heavy metals and pesticides. Unlike previous reports focusing on the relationships among PMs, wastewater discharge and population distribution, this work innovatively studied the distribution characteristics of pollutants by principal components analysis. The results suggest that PMs can be used as a chemical marker indicating domestic contamination. PMID:23508139

  12. The Origins of Polycyclic Aromatic Hydrocarbons: Are They Everywhere?

    Science.gov (United States)

    Allamandola, L. J.; Morrison, David (Technical Monitor)

    1994-01-01

    During the past 15 years considerable progress in observational techniques has been achieved in the middle-infrared region (5000-500 per centimeter, 2-20 micron), the region where most diagnostic molecular vibrations occur. Spectra of many different astronomical infrared sources, some deeply embedded in dark molecular clouds and others at their edges, are now available. These spectra provide a powerful probe, not only for the identification of interstellar molecules in both the gas and solid phases, but also of the physical and chemical conditions which prevail in these two very different domains. The two lectures will focus on the evidence that polycyclic aromatic hydrocarbons (PAHs) are an important, ubiquitous and abundant interstellar species. PAHs are. extremely stable species which can range in size from a few angstroms across to several hundred angstroms (PAHs are also the building blocks of amorphous carbon particles). This identification rests on the suggestive agreement between the laboratory spectra of PAHs with a set of IR emission bands which emanate from many different sources where ultraviolet starlight impinges on a "dusty" region. The picture is that individual PAHs are first pumped into highly vibrationally excited states and relax by fluorescence at their fundamental vibrational frequencies. That PAHs are a ubiquitous interstellar component has serious ramifications in other spectral regions as well, including the strong extinction in the ultraviolet, and the classic visible diffuse interstellar bands discovered more than 50 years ago (but unexplained to this day) The first part of the course will focus on the interpretation of astronomical spectra. The second lecture will start by showing how recent laboratory data on PAHs taken under realistic interstellar conditions has con borated the PAH hypothesis and led to great insight into the conditions in the PAH containing regions. This lecture will end by reviewing the ever-increasing evidence for

  13. POLYCYCLIC AROMATIC HYDROCARBON FAR-INFRARED SPECTROSCOPY

    International Nuclear Information System (INIS)

    The far-IR characteristics of astrophysically relevant polycyclic aromatic hydrocarbons (PAHs) averaging in size around 100 carbon atoms have been studied using the theoretical spectra in the NASA Ames PAH IR Spectroscopic Database. These spectra were calculated using density functional theory. Selections of PAH species are made, grouped together by common characteristics or trends, such as size, shape, charge, and composition, and their far-IR spectra compared. The out-of-plane modes involving the entire molecule are explored in detail, astronomical relevance is assessed, and an observing strategy is discussed. It is shown that PAHs produce richer far-IR spectra with increasing size. PAHs also produce richer far-IR spectra with increasing number of irregularities. However, series of irregular-shaped PAHs with the same compact core have common 'Jumping-Jack' modes that 'pile up' at specific frequencies in their average spectrum. For the PAHs studied here, around 100 carbon atoms in size, this band falls near 50 μm. PAH charge and nitrogen inclusion affect band intensities but have little effect on far-IR band positions. Detailed analysis of the two-dimensional, out-of-plane bending 'drumhead' modes in the coronene and pyrene 'families' and the one-dimensional, out-of-plane bending 'bar' modes in the acene 'family' show that these molecular vibrations can be treated as classical vibrating sheets and bars of graphene, respectively. The analysis also shows that the peak position of these modes is very sensitive to the area of the emitting PAH and does not depend on the particular geometry. Thus, these longest wavelength PAH bands could provide a unique handle on the size of the largest species in the interstellar PAH family. However, these bands are weak. Observing highly excited regions showing the mid-IR bands in which the emission from classical dust peaks at short wavelengths offers the best chance of detecting PAH emission in the far-IR. For these regions

  14. Atmospheric contamination

    International Nuclear Information System (INIS)

    It is about the levels of contamination in center America, the population's perception on the problem, effects of the atmospheric contamination, effects in the environment, causes of the atmospheric contamination, possibilities to reduce the atmospheric contamination and list of Roeco Swisscontac in atmospheric contamination

  15. Particulate Organic Matter (POM) Separation

    International Nuclear Information System (INIS)

    Information on soil organic matter (SOM) pools is of vital importance for studying the impact of soil management and environmental factors on soil organic carbon, an important part of the global carbon cycle. Several conceptual SOM pools with different turnover rates are available to feed models or to study carbon cycles. The fractionation scheme of Zimmermann allows isolating the labile particulate organic matter (POM) pool. Besides its use in conventional soil organic carbon dynamics studies and modelling, this pool can be determining as well in the evaluation of soil organic carbon stability based on the use of stable 15N and 13C isotopes

  16. Particulate residue separators for harvesting devices

    Science.gov (United States)

    Hoskinson, Reed L.; Kenney, Kevin L.; Wright, Christopher T.; Hess, John R.

    2010-06-29

    A particulate residue separator and a method for separating a particulate residue stream may include a plenum borne by a harvesting device, and have a first, intake end and a second, exhaust end; first and second particulate residue air streams which are formed by the harvesting device and which travel, at least in part, along the plenum and in a direction of the second, exhaust end; and a baffle assembly which is located in partially occluding relation relative to the plenum, and which substantially separates the first and second particulate residue air streams.

  17. Methods of separating particulate residue streams

    Science.gov (United States)

    Hoskinson, Reed L.; Kenney, Kevin L.; Wright, Christopher T.; Hess, J. Richard

    2011-04-05

    A particulate residue separator and a method for separating a particulate residue stream may include an air plenum borne by a harvesting device, and have a first, intake end and a second, exhaust end; first and second particulate residue air streams that are formed by the harvesting device and that travel, at least in part, along the air plenum and in a direction of the second, exhaust end; and a baffle assembly that is located in partially occluding relation relative to the air plenum and that substantially separates the first and second particulate residue air streams.

  18. Particulate Matter (Environmental Health Student Portal)

    Science.gov (United States)

    ... Air Pollution Home Indoor Air Pollution Outdoor Air Pollution Particulate Matter Ozone Chemicals Chemicals Home Mercury Lead Arsenic Volatile Organic Compounds Plastics Pesticides Climate Change Climate ...

  19. Mass balances on selected polycyclic aromatic hydrocarbons in the New York-New Jersey Harbor.

    Science.gov (United States)

    Rodenburg, Lisa A; Valle, Sandra N; Panero, Marta A; Muñoz, Gabriela R; Shor, Leslie M

    2010-01-01

    Mass balances on 10 polycyclic aromatic hydrocarbons (PAHs) in the New York-New Jersey Harbor (hereafter "the Harbor") were constructed using monitoring data from the water column, sediment, and atmosphere. Inputs considered included tributaries, atmospheric deposition, wastewater treatment plant discharges, combined sewer overflows (CSOs), and stormwater runoff. Removal processes examined included tidal exchange between the Harbor and the coastal Bight and Long Island Sound, volatilization, and accumulation or burial of sediment-bound PAHs in the Harbor. The PAHs investigated were fluorene, phenanthrene, fluoranthene, pyrene, benz[a]anthracene, benzo[a]pyrene, perylene, benzo[ghi]perylene, indeno[1,2,3-cd]pyrene, and dibenz[a,h]anthracene. The results show inputs and outputs are fairly well balanced for most compounds, a finding that suggests aerobic biodegradation may not be a key loss process in this Harbor, as has been assumed in other systems. The main pathway for inputs of all PAHs is stormwater runoff. Atmospheric deposition is an important conveyor of PAHs with molecular weights sustainable management of urban water resources. PMID:20176837

  20. Scavenging ratio of polycyclic aromatic compounds in rain and snow at the Athabasca oil sands region

    Directory of Open Access Journals (Sweden)

    L. Zhang

    2014-07-01

    Full Text Available Athabasca oil sands industry in northern Alberta, Canada is a possible source of polycyclic aromatic compounds (PACs. Monitored PACs, including polycyclic aromatic hydrocarbons (PAHs, alkylated PAHs, and dibenzothiophenes, in precipitation and in air at three near-source sites in the Fort MacKay and Fort McMurray area during May 2011 to August 2012 were analyzed to generate a database of scavenging (or washout ratios (Wt for PACs scavenged by both snow and rain. Median precipitation and air concentrations of parent PAHs over the May 2011 to August 2012 period ranged from 0.3–184.9 (chrysene ng L−1 and 0.01–3.9 (naphthalene ng m−3, respectively, which were comparable to literature values. Higher concentrations in precipitation and air were observed for alkylated PAHs and dibenzothiophenes. The median precipitation and air concentrations were 11.3–646.7 (C3-fluoranthene/pyrene ng L−1 and 0.21–16.9 (C3-naphthalene ng m−3, respectively, for alkylated PAHs, and 8.5–530.5 (C4-dibenzothiophene ng L−1 and 0.13–6.6 (C2-dibenzothiophene ng m−3 for dibenzothiophenes and their alkylated derivatives. Median Wt over the measurement period were 6100–1.1 × 106 from snow scavenging and 350–2.3 × 105 from rain scavenging depending on the PAC species. Median Wt for parent PAHs were within the range of those observed at other urban and suburban locations. But Wt for acenaphthylene in snow samples was 2–7 times higher. Some individual snow and rain samples exceeded literature values by a factor of 10. Wt for benzo(apyrene, dibenz(a,hanthracene, and benzo(g,h,iperylene in snow samples had reached 107, which is the maximum for PAH snow scavenging ratios reported in literature. From the analysis of data subsets, Wt for particulate-phase dominant PACs were 14–20 times greater than gas-phase dominant PACs in snow samples and 7–20 times greater than gas-phase dominant PACs in rain samples. Wt from snow scavenging was ∼9 times greater

  1. 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").

  2. Ambient air concentrations of polycyclic aromatic hydrocarbons in Germany

    Energy Technology Data Exchange (ETDEWEB)

    Beck, E.M. [Landesanstalt fuer Umweltschutz Baden-Wuerttemberg, Karlsruhe (Germany)

    1999-10-01

    Polycyclic aromatic hydrocarbons (PAHs) have been measured in most of the German states. The measurements were carried out under different seasonal conditions and at locations with differing air quality. Benzo(a)pyrene was widely used as an indicator substance for heating systems and industrial firing systems. Coronene and benzo(g,h,i)perylene were used as indicator substances for motor traffic.

  3. Photolytic and radiolytic destruction of natural polycyclic mycotoxins

    International Nuclear Information System (INIS)

    Full text: The kinetics of degradation of natural polycyclic toxins in grains and dried fruits under the influence of UV-light and ionizing radiation 60C and the probability of radiolytic detoxication of these products has been studied for the first time

  4. Bioavailability of Polycyclic Aromatic Hydrocarbons in Soils and Sediments

    NARCIS (Netherlands)

    Cuypers, M.P.

    2001-01-01

    Polycyclic aromatic hydrocarbons (PAHs) constitute a group of priority pollutants which are of increasing environmental concern because of their adverse effects on humans, animals, and plants. Soils and sediments generally serve as a sink for PAHs, which leads to the accumulation of PAHs at contamin

  5. Extraction Techniques for Polycyclic Aromatic Hydrocarbons in Soils

    OpenAIRE

    Lau, E. V.; Gan, S.; Ng, H.K.

    2010-01-01

    This paper aims to provide a review of the analytical extraction techniques for polycyclic aromatic hydrocarbons (PAHs) in soils. The extraction technologies described here include Soxhlet extraction, ultrasonic and mechanical agitation, accelerated solvent extraction, supercritical and subcritical fluid extraction, microwave-assisted extraction, solid phase extraction and microextraction, thermal desorption and flash pyrolysis, as well as fluidised-bed extraction. The influencing factors in ...

  6. AGRONOMIC OPTIMIZATION FOR PHYTOREMEDIATION OF POLYCYCLIC AROMATIC HYDROCARBONS

    Science.gov (United States)

    Phytoremediation is a low-cost method of using plants to degrade, volatilize or sequester organic and metal pollutants that has been used in efforts to remediate sites contaminated with polycyclic aromatic hydrocarbon (PAH) refinery wastes. Non-native plant species aggressivel...

  7. Polycyclic aromatic hydrocarbons in air samples of meat smokehouses

    DEFF Research Database (Denmark)

    Hansen, Åse Marie; Olsen, I L; Poulsen, O M

    In a screening programme nine Danish meat smokehouses were randomly selected for measurements on concentration of airborne polycyclic aromatic hydrocarbons (PAH). A total of 23 stationary air samples were collected during the entire working period of the kiln either above the kiln doors or...

  8. Experimental determination of structural parameters in selected polycyclic aromatic compounds

    Czech Academy of Sciences Publication Activity Database

    Dračínský, Martin; Císařová, I.; Storch, Jan; Sýkora, Jan

    Ozarow Mazowiecki : Nobell Congressing, 2015 - (Kosinski, K.; Urbanczyk, M.; Zerko, S.). s. 81 [Magnetic Moments in Central Europe 2015. 25.02.2015-01.03.2015, Krynica-Zdrój] R&D Projects: GA ČR GA15-12719S Institutional support: RVO:61388963 ; RVO:67985858 Keywords : polycyclic aromatic compounds * NMR * DFT Subject RIV: CF - Physical ; Theoretical Chemistry

  9. Extraction of polycyclic aromatic nitrogen heterocycles from spiked soil samples

    Czech Academy of Sciences Publication Activity Database

    Kočí, K.; Petrovská, H.; Šimek, Z.; Varaďová-Ostrá, Elena; Syslová, A.

    2007-01-01

    Roč. 87, č. 2 (2007), s. 111-123. ISSN 0306-7319 Institutional research plan: CEZ:AV0Z40310501 Keywords : polycyclic aromatic nitrogen heterocycle * supercritical fluid extraction * Soxhlet Subject RIV: CB - Analytical Chemistry, Separation Impact factor: 1.026, year: 2007

  10. Abundance and distribution of gaseous ammonia and particulate ammonium at Delhi (India)

    Science.gov (United States)

    Singh, S.; Kulshrestha, U. C.

    2012-01-01

    This study reports abundance and distribution of gaseous NH3 and particulate NH4+ at Delhi. Gaseous NH3 and particulate NH4+ concentrations were measured during pre monsoon, monsoon and postmonsoon seasons of the years 2010 and 2011. Average concentrations of gaseous NH3 during premonsoon, monsoon and post monsoon seasons were recorded as 26.4, 33.2 and 32.5 μg m-3, respectively. Gaseous NH3 concentrations were the highest during monsoon due to decay and decomposition of plants and other biogenic material under wet conditions which emit NH3. The results showed that particulate NH4+ was always lower than the gaseous NH3 during all the seasons. The concentrations of particulate NH4+ were recorded as 11.6, 22.9 and 8.5 μg m-3 during premonsoon, monsoon and postmonsoon seasons, respectively. The percent fraction of particulate NH4+ was noticed highest during monsoon season due to increased humidity levels. On anaverage, 33.3 % of total N-NHx was present as particulate NH4+. Higher concentrations of NH3 noticed during night time may be due to stable atmospheric conditions. Study highlighted that as compared to rural sites, urban sites showed higher concentrations of gaseous NH3 in India which may be due to higher population density, human activities and poor sanitation arrangements.

  11. Sub-micrometre particulate matter is primarily in liquid form over Amazon rainforest

    Science.gov (United States)

    Bateman, Adam P.; Gong, Zhaoheng; Liu, Pengfei; Sato, Bruno; Cirino, Glauber; Zhang, Yue; Artaxo, Paulo; Bertram, Allan K.; Manzi, Antonio O.; Rizzo, Luciana V.; Souza, Rodrigo A. F.; Zaveri, Rahul A.; Martin, Scot T.

    2016-01-01

    Atmospheric particulate matter influences the Earth’s energy balance directly, by altering or absorbing solar radiation, and indirectly by influencing cloud formation. Whether organic particulate matter exists in a liquid, semi-solid, or solid state can affect particle growth and reactivity, and hence particle number, size and composition. The properties and abundance of particles, in turn, influence their direct and indirect effects on energy balance. Non-liquid particulate matter was identified over a boreal forest of Northern Europe, but laboratory studies suggest that, at higher relative humidity levels, particles can be liquid. Here we measure the physical state of particulate matter with diameters smaller than 1 μm over the tropical rainforest of central Amazonia in 2013. A real-time particle rebound technique shows that the particulate matter was liquid for relative humidity greater than 80% for temperatures between 296 and 300 K during both the wet and dry seasons. Combining these findings with the distributions of relative humidity and temperature in Amazonia, we conclude that near-surface sub-micrometre particulate matter in Amazonia is liquid most of the time during both the wet and the dry seasons.

  12. Particulate accumulations in the vital organs of wild Brevoortia patronus from the northern Gulf of Mexico after the Deepwater Horizon oil spill.

    Science.gov (United States)

    Millemann, Daniel R; Portier, Ralph J; Olson, Gregory; Bentivegna, Carolyn S; Cooper, Keith R

    2015-11-01

    Histopathologic lesions were observed in the commercially important filter-feeding fish, Brevoortia patronus (Gulf menhaden), along the Louisiana Gulf Coast. Menhaden collected from Louisiana waters in 2011 and 2012, 1 and 2 years following the Deepwater Horizon oil spill, showed varying severities of gill lesions as well as an unusual accumulation of black particulates visible at necropsy in the heart and stomach vasculature. The PAH derived particulates were typically 1-4 µm in diameter, but larger aggregates were observed in the coronary vessels on the ventricle surfaces and their location and size was confirmed by light microscopy. Composited particulate composition was consistent with weathered petrogenic polycyclic aromatic hydrocarbon (PAH) mixtures based on GC-MS analysis. Particulate