WorldWideScience

Sample records for atmospheric particulate polycyclic

  1. 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.

  2. [Pollution of Halogenated Polycyclic Aromatic Hydrocarbons in Atmospheric Particulate Matters of Shenzhen].

    Science.gov (United States)

    Sun, Jian-lin; Chang, Wen-jing; Chen, Zheng-xia; Zeng, Hui

    2015-05-01

    Concentrations of halogenated polycyclic aromatic hydrocarbons ( HPAHs) in atmospheric PM10 and PM2.5 samples collected from Shenzhen were determined using GC-MS. Total concentrations of nine HPAHs in atmospheric PM10 and PM2.5 samples ranged from 118 to 1,476 pg · m(-3) and 89 to 407 pg · m(-3), respectively. In PM10 and PM(2.5) samples, the concentration of 9-BrAnt was the highest, followed by 7-BrBaA and 9, 10-Br2Ant. Seasonal levels of total HPAHs in atmospheric PM10 and PM2.5 samples in Shenzhen decreased in the following order: winter > autumn > spring > summer, whereas concentrations of individual HPAHs showed different seasonal levels. Meteorological conditions, including temperature, precipitation, and relative humidity, might be important factors affecting the seasonal levels of HPAHs in atmospheric PM10 and PM2.5 In addition, there were significant correlations between concentrations of HPAHs and parent PAHs. Finally, the toxic equivalency quotients (TEQs) of HPAHs were estimated. The TEQs of HPAHs in atmospheric PM10 and PM2.5 samples ranged from 17.6 to 86.2 pg · m(-3) and 14.6 to 70.4 pg · m(-3), respectively. Among individual HPAHs, 7-BrBaA contributed greatly to the total TEQs of HPAHs. Our results indicated that the total TEQs of HPAHs were lower than parent PAHs in atmospheric PM10 and PM2.5 samples in Shenzhen.

  3. Analysis of atmospheric concentrations of quinones and polycyclic aromatic hydrocarbons in vapour and particulate phases

    Science.gov (United States)

    Delgado-Saborit, Juana Maria; Alam, Mohammed S.; Godri Pollitt, Krystal J.; Stark, Christopher; Harrison, Roy M.

    2013-10-01

    Polycyclic aromatic hydrocarbons (PAH) are often measured in studies of atmospheric chemistry or health effects of air pollution, due to their known human carcinogenicity. In recent years, PAH quinone derivatives have also become a focus of interest, primarily because they can contribute to oxidative stress. This work reports concentrations of 17 PAH and 15 quinones measured in air samples collected at a trafficked roadside. Data are presented for four compounds not previously reported in ambient air: 2-methyl-1,4-naphthoquinone, 2,6-di-tert-butyl-1,4-benzoquinone, methyl-1,4-benzoquinone and 2,3-dimethylanthraquinone, and a large vapour phase component is measured, not analysed in most earlier studies. Analyses are reported also for SRM 1649a and 1649b, including many compounds (8 for SRM 1649a and 12 for SRM 1649b) for which concentrations have not previously been reported. This work assesses the vapour/particle phase distribution of PAHs and quinones in relation to their molecular weight, vapour pressure, polarity and Henry's Law constant, finding that both molecular weight and vapour pressure (which are correlated) are good predictors of the partitioning.

  4. Atmospheric behaviors of particulate-bound polycyclic aromatic hydrocarbons and nitropolycyclic aromatic hydrocarbons in Beijing, China from 2004 to 2010

    Science.gov (United States)

    Tang, Ning; Suzuki, Genki; Morisaki, Hiroshi; Tokuda, Takahiro; Yang, Xiaoyang; Zhao, Lixia; Lin, Jinming; Kameda, Takayuki; Toriba, Akira; Hayakawa, Kazuichi

    2017-03-01

    Airborne particulates were collected at an urban site (site 1) from 2004 to 2010 and at a suburban site (site 2) in 2010 in Beijing. Nine polycyclic aromatic hydrocarbons (PAHs) and five nitropolycyclic aromatic hydrocarbons (NPAHs) in the airborne particulates were determined by HPLC with fluorescence and chemiluminescence detection, respectively. The concentrations of PAHs and NPAHs were higher in heating season than in non-heating season at the two sites. Both the concentrations of PAHs and NPAHs decreased in the non-heating season but only the concentrations of NPAHs decreased in heating season at site 1, from 2004 to 2010. These findings suggest that source control measures implemented by the city of Beijing helped to reduce air pollution in Beijing. The concentrations of PAHs increased at site 1 in 2010, possibly because of the transport of emissions from windward other areas, such as Shanxi province. Several diagnostic ratios of PAHs and NPAHs showed that the different sources contributed to Beijing's air pollution, although coal combustion was the main source in the heating season and vehicle emission was the main source in the non-heating season. An analysis of physical parameters at Beijing showed that high wind speed can remove atmospheric PAHs and NPAHs in the heating season and that high relative humidity can remove them in the non-heating season.

  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. Photodynamic bioassay of polycyclic atmospheric pollutants

    Energy Technology Data Exchange (ETDEWEB)

    Epstein, S.S.; Small, M.; Sawicki, E.; Falk, H.L.

    1965-04-01

    A photodynamic bioassay which can be conducted on one mgm amounts of organic atmospheric particulates is described, using Paramecium caudatum. The results of a pilot study on pollutants from several American cities indicate that the assay may provide a rapid, simple and economical biological index of a potential carcinogenic hazard attributable to polycyclic compounds. The utility of the assay for this purpose is under further evaluation. 15 references, 5 figures, 1 table.

  7. 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...

  8. Polycyclic Aromatic Hydrocarbons in Fine Particulate Matter ...

    Science.gov (United States)

    This study measured polycyclic aromatic hydrocarbon (PAH) composition in particulate matter emissions from residential cookstoves. A variety of fuel and cookstove combinations were examined, including: (i) liquid petroleum gas (LPG), (ii) kerosene in a wick stove, (iii) wood (10% and 30% moisture content on a wet basis) in a forced-draft fan stove, and (iv) wood in a natural-draft rocket cookstove. LPG combustion had the highest thermal efficiency (~57%) and the lowest PAH emissions per unit fuel energy, resulting in the lowest PAH emissions per useful energy delivered (MJd). The average benzo[a]pyrene (B[a]P) emission factor for LPG was 0.842 µg/MJd; the emission rate was 0.043 µg/min. The highest PAH emissions were from wood burning in the natural-draft stove (209-700 µg B[a]P/MJd). PAH emissions from kerosene were significantly lower than those from the wood burning in the natural-draft cookstove, but higher than those from LPG. It is expected that in rural regions where LPG and kerosene are unavailable or unaffordable, the forced-draft fan stove may be an alternative because its emission factor (5.17-8.07 µg B[a]P/MJd) and emission rate (0.52-0.57 µg/min) are similar to kerosene (5.36 µg B[a]P/MJd and 0.45 µg/min). Compared with wood combustion emissions, LPG stoves emit less total PAH emissions and less fractions of high molecular weight PAHs. Relatively large variations in PAH emissions from LPG call for additional future tests to identify the major

  9. Polycyclic aromatic hydrocarbon in fine particulate matter emitted from burning kerosene, liquid petroleum gas, and wood fuels in household cookstoves

    Data.gov (United States)

    U.S. Environmental Protection Agency — This dataset includes all data in figures in the manuscript and supporting information for the publication entitled "Particulate polycyclic aromatic hydrocarbon...

  10. Exposure of Firefighters to Particulates and Polycyclic Aromatic Hydrocarbons

    Science.gov (United States)

    Baxter, C. Stuart; Hoffman, Joseph D.; Knipp, Michael J.; Reponen, Tiina; Haynes, Erin N.

    2015-01-01

    Firefighting continues to be among the most hazardous yet least studied occupations in terms of exposures and their relationship to occupational disease. Exposures are complex, involving mixtures of particles and chemicals such as polycyclic aromatic hydrocarbons (PAHs). Adverse health effects associated with these agents include elevated incidences of coronary heart disease and several cancers. PAHs have been detected at fire scenes, and in the firehouse rest area and kitchen, routinely adjoining the truck bay, and where firefighters spend a major part of each shift. An academic-community partnership was developed with the Cincinnati Fire Department with the goal of understanding active firefighters' airborne and dermal PAH exposure. PAHs were measured in air and particulates, and number and mass concentrations, respectively, of submicron (0.02–1 μm) and PM2.5 (2.5 μm diameter and less) particles during overhaul events in two firehouses and a University of Cincinnati administrative facility as a comparison location. During overhaul firefighters evaluate partially combusted materials for re-ignition after fire extinguishment and commonly remove Self-Contained Breathing Apparatus (SCBA). Face and neck wipes were also collected at a domestic fire scene. Overhaul air samples had higher mean concentrations of PM2.5 and submicron particles than those collected in the firehouse, principally in the truck bay and kitchen. Among the 17 PAHs analyzed, only naphthalene and acenaphthylene were generally detectable. Naphthalene was present in 7 out of 8 overhaul activities, in 2 out of 3 firehouse (kitchen and truck bay) samples, and in none collected from the control site. In firefighter face and neck wipes a greater number of PAHs were found, several of which have carcinogenic activity, such as benzofluoranthene, an agent also found in overhaul air samples. Although the concentration for naphthalene, and all other individual PAHs, was very low, the potential simultaneous

  11. Polycyclic Aromatic Hydrocarbons in Fine Particulate Matter Emitted from Burning Kerosene, Liquid Petroleum Gas, and Wood Fuels in Household Cookstoves

    Science.gov (United States)

    This study measured polycyclic aromatic hydrocarbon (PAH) composition in particulate matter emissions from residential cookstoves. A variety of fuel and cookstove combinations were examined, including: (i) liquid petroleum gas (LPG), (ii) kerosene in a wick stove, (iii) wood (10%...

  12. Upper Atmospheric Particulate Monitoring and Sample Return

    Science.gov (United States)

    Liddell, Alan; Sohl, John E.

    2010-10-01

    H.A.R.B.O.R. (High Altitude Reconnaissance Balloon for Outreach and Research) is a student-run program in which high-altitude balloon systems are designed, constructed, and flown by students conducting individual or group research projects. One area of interest is in the sampling of particles in the upper atmosphere. Collecting airborne particulates and studying them under an SEM can answer questions on the origins of airborne particulate matter. We could find explanations for climate change or directly measure pollution caused by smokestacks. The SEM has the capacity to capture images of particulates and determine their composition. I am building a system capable of sampling air up to 30km (100,000 ft). The system will contain a servo-controlled filter system for sampling air captured by the ascent of the balloon. Currently, filter types are being evaluated for capture rate and air flow resistance. A circuit has been built to test the mass throughput of the airflow as the balloon travels its course. A vacuum chamber is being built to simulate the nearspace environment. Testing and simulation should be complete in time to fly a finalized sample return mission in spring 2011.

  13. Measurement of particulate phase polycyclic aromatic hydrocarbon (PAHs) around a petroleum refinery.

    Science.gov (United States)

    Rao, Padma S; Ansari, M Faiyaz; Pipalatkar, P; Kumar, A; Nema, P; Devotta, S

    2008-02-01

    A study on concentrations of ambient particulates viz. total suspended particulate matters (TSP), respirable suspended particulate matter (RSPM) and polycyclic aromatic hydrocarbons (PAH) were carried out at six sites around the Asia's largest, 12 MMTPA, petroleum refinery in west coast of India. PAH concentrations are correlated with each other in these sites, suggesting that they have related sources and sinks. The present article discusses the monitoring aspects such as sample collection, pretreatment and analytical methods and compares the monitored levels for assessing the source receptor distribution pattern. The main sources of RSPM and PAHs in urban air are automobile exhaust (CPCB, Polycyclic aromatic hydrocarbons (PAHs) in air and their effects on human health. " http://www.cpcb.nic.in/ph/ch21103.htm ", 2003; Manuel et al., Environmental Science and Technology, 13: 227-231, 2004) and industrial emissions like petroleum refinery (Vo-Dinh, Chemical analysis of polycyclic aromatic hydrocarbons, Wiley: New York, 1989; Wagrowaski and Hites, Environmental Science and Technology, 31: 279-282, 1997). Polycyclic aromatic hydrocarbons (PAH) are ubiquitous constituents of urban airborne particulate mostly generated by anthropogenic activities (Li et al., Environmental Science and Technology, 37:1958-2965, 2003; Thorsen et al., Environmental Science and Technology, 38: 2029-2037, 2004; Ohura et al., Environmental Science and Technology, 32: 450-455, 2004) and some of them are of major health concern mainly due to their well-known carcinogenic and mutagenic properties (Soclo et al., Marine Pollution Bulletin, 40: 387-396, 2000; Chen et al., Environment International, 28: 659-668, 2003; Larsen and Baker, Environmental Science and Technology, 32: 450-455, 2003). Limited information is available on PAHs contributions from refineries to ambient air. Hence this study would not only create a database but also provide necessary inputs towards dose-response relationship for

  14. A new method for the simultaneous determination of PAH and metals in samples of atmospheric particulate matter

    Science.gov (United States)

    Piñeiro-Iglesias, M.; López-Mahía, P.; Muniategui-Lorenzo, S.; Prada-Rodríguez, D.; Querol, X.; Alastuey, A.

    A method for the analysis of polycyclic aromatic hydrocarbons (PAH) and metals in the same filter portion employed for atmospheric particulate samples collection is proposed in this study. Two standard reference materials, SRM 1648 and SRM 1649a, were extracted by microwave-assisted extraction with hexane/acetone (1:1) and the solid residue was acid digested for the determination of levels of metals. It is demonstrated that there were no significant losses of the metal load during the PAH extraction process. Finally, the devised methodology was applied to actual atmospheric particulate samples.

  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. In-situ observation of atmospheric particulates

    Science.gov (United States)

    Harrison, William Alan

    Airborne particulates play a central role in both the earth’s radiation balance and as a trigger for a wide range of health impacts. Air quality monitors are placed in networks across many cities globally. Typically these provide at best a few recording locations per city. However, large spatial variability occurs on the neighborhood scale. This study sets out to comprehensively characterize a full size distribution from 0.25 - 32 μm of airborne particulates on a fine spatial scale (meters). To fully characterize the impact of atmospheric particulates, global scale observations and data products are needed. Satellite products allow for this global coverage but require in situ validations. For the first part of this study data is gathered on a near daily basis over the month of May, 2014 in a 100 km2 area encompassing parts of Richardson, Texas, and Garland, Texas. Wind direction was determined to be the dominant factor in classifying the data. The highest mean PM2.5 concentration was 14.1 ± 5.7 μgm. -3 corresponding to periods when the wind was out of the south. The lowest PM2.5 concentrations were observed after several consecutive days of rainfall. The rainfall was found to not only “cleanse” the air, leaving a mean PM2.5 concentration as low as 3.0 ± 0.5 μgm. -3 , but to leave the region with a more uniform PM2.5 concentration. Variograms were used to determine an appropriate spatial scale for future sensor placement to provide measurements on a neighborhood scale and found that the spatial scales varied, depending on the synoptic weather pattern, from 0.8 km to 5.2 km, with a typical length scale of 1.7 km. This second part of this study used a zero emission remote-controlled aerial vehicle to look at the horizontal, vertical, and temporal variability of airborne particulates within the first 140 m of the atmosphere. Four flights where conducted on December 4, 2014 between 12:00 pm and 5:00 pm local time. The first three flights flew a pattern of

  17. Challenges in tracing the fate and effects of atmospheric polycyclic aromatic hydrocarbon deposition in vascular plants.

    Science.gov (United States)

    Desalme, Dorine; Binet, Philippe; Chiapusio, Geneviève

    2013-05-07

    Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous organic pollutants that raise environmental concerns because of their toxicity. Their accumulation in vascular plants conditions harmful consequences to human health because of their position in the food chain. Consequently, understanding how atmospheric PAHs are taken up in plant tissues is crucial for risk assessment. In this review we synthesize current knowledge about PAH atmospheric deposition, accumulation in both gymnosperms and angiosperms, mechanisms of transfer, and ecological and physiological effects. PAHs emitted in the atmosphere partition between gas and particulate phases and undergo atmospheric deposition on shoots and soil. Most PAH concentration data from vascular plant leaves suggest that contamination occurs by both direct (air-leaf) and indirect (air-soil-root) pathways. Experimental studies demonstrate that PAHs affect plant growth, interfering with plant carbon allocation and root symbioses. Photosynthesis remains the most studied physiological process affected by PAHs. Among scientific challenges, identifying specific physiological transfer mechanisms and improving the understanding of plant-symbiont interactions in relation to PAH pollution remain pivotal for both fundamental and applied environmental sciences.

  18. Atmospheric transport and outflow of polycyclic aromatic hydrocarbons from China.

    Science.gov (United States)

    Lang, Chang; Tao, Shu; Liu, Wenxin; Zhang, Yanxu; Simonich, Staci

    2008-07-15

    A potential receptor influence function (PRIF) model, based on air mass forward trajectory calculations, was applied to simulate the atmospheric transport and outflow of polycyclic aromatic hydrocarbons (PAHs) emitted from China. With a 10 day atmospheric transport time, most neighboring countries and regions, as well as remote regions, were influenced by PAH emissions from China. Of the total annual PAH emission of 114 Gg, 92.7% remained within the boundary of mainland China. The geographic distribution of PRIFs within China was similar to the geographic distribution of the source regions, with high values in the North China Plain, Sichuan Basin, Shanxi, and Guizhou province. The Tarim basin and Sichuan basin had unfavorable meteorological conditions for PAH outflow. Of the PAH outflow from China (8092 tons or 7.1% of the total annual PAH emission), approximately 69.9% (5655 tons) reached no further than the offshore environment of mainland China and the South China Sea. Approximate 227, 71, 746, and 131 tons PAHs reached North Korea, South Korea, Russia-Mongolia region, and Japan, respectively, 2-4 days after the emission. Only 1.4 tons PAHs reached North America after more than 9 days. Interannual variation in the eastward PAH outflow was positively correlated to cold episodes of El Niño/Southern Oscillation. However, trans-Pacific atmospheric transport of PAHs from China was correlated to Pacific North America index (PNA) which is associated with the strength and position of westerly winds.

  19. Atmospheric transport and outflow of polycyclic aromatic hydrocarbons from China

    Energy Technology Data Exchange (ETDEWEB)

    Chang Lang; Shu Tao; Wenxin Liu; Yanxu Zhang; Staci Simonich [Peking University, Beijing (China). Laboratory for Earth Surface Processes, College of Environmental Sciences

    2008-07-15

    A potential receptor influence function (PRIF) model, based on air mass forward trajectory calculations, was applied to simulate the atmospheric transport and outflow of polycyclic aromatic hydrocarbons (PAHs) emitted from China. With a 10 day atmospheric transport time, most neighboring countries and regions, as well as remote regions, were influenced by PAH emissions from China. Of the total annual PAH emission of 114 Gg, 92.7% remained within the boundary of mainland China. The geographic distribution of PRIFs within China was similar to the geographic distribution of the source regions, with high values in the North China Plain, Sichuan Basin, Shanxi, and Guizhou province. The Tarim basin and Sichuan basin had unfavorable meteorological conditions for PAH outflow. Of the PAH outflow from China (8092 tons or 7.1% of the total annual PAH emission), approximately 69.9% (5655 tons) reached no further than the offshore environment of mainland China and the South China Sea. Approximate 227, 71, 746, and 131 tons PAHs reached North Korea, South Korea, Russia-Mongolia region, and Japan, respectively, 2-4 days after the emission. Only 1.4 tons PAHs reached North America after more than 9 days. Interannual variation in the eastward PAH outflow was positively correlated to cold episodes of El Nino/Southern Oscillation. However, trans-Pacific atmospheric transport of PAHs from China was correlated to Pacific North America index (PNA) which is associated with the strength and position of westerly winds. 38 refs., 4 figs.

  20. Atmospheric trace metal concentrations in Suspended Particulate ...

    African Journals Online (AJOL)

    The particulate samples from where the metals were characterized and quantified, were collected between December 2007 and March 2008, using a Gravimetric technique a portable SKC 506673 High volume Gravimetric sampler. The air particulate samples were collected from the kitchens, living rooms and outdoor ...

  1. Health effects of atmospheric particulates: a medical geology perspective.

    Science.gov (United States)

    Duzgoren-Aydin, Nurdan S

    2008-01-01

    In this review, atmospheric particulates as composite airborne earth materials often containing both natural and anthropogenic components were examined in the context of medical geology. Despite a vast number of both experimental and epidemiological studies confirming the direct and indirect links between atmospheric particulates and human health, the exact nature of mechanisms affecting the particulate-induced pathogenesis largely remains unexplored. Future in depth research on these areas would be most successful if potential mechanisms are examined with reference to the physical (e.g., size, shape and surface), chemical, mineralogical and source characteristics of particulate matters. The underlying goal of this review was to present the relevant terminology and processes proposed in the literature to explain the interfaces and interactions between atmospheric particles and human body within the framework of "atmospheric particle cycles." The complexities of the interactions were demonstrated through case studies focusing on particulate matter air pollution and malignant mesothelioma occurrences due to environmental exposure to erionite-a fibrous zeolite mineral. There is an urgent need for a standard protocol or speciation methods applicable to earth-materials to guide and streamline studies on etiology of mineral-induced diseases. This protocol or speciation methods should provide relevant procedures to determine the level and extent of physical, chemical and mineralogical heterogeneity of particulate matters as well as quantitative in-situ particulate characteristics.

  2. 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.

  3. Correlation of levels of volatile versus carcinogenic particulate polycyclic aromatic hydrocarbons in air samples from smokehouses

    DEFF Research Database (Denmark)

    Hansen, Åse Marie; Poulsen, O M; Christensen, J M

    1991-01-01

    In the present study, data on the concentration of polycyclic aromatic hydrocarbons (PAH) in air samples from fish smokehouses (Nordholm et al. 1986) and meat smokehouses (Hansen et al. submitted for publication) were used to analyze the extent to which six different volatile PAH compounds could...... function as markers for the total concentration of six different carcinogenic particulate PAH compounds. Although a significant positive correlation was observed between the concentration of each of six volatile compounds and the total concentration of carcinogenic PAH compounds, a particularly good...... carcinogenic PAH compounds in air samples from smokehouses, whereas fluoranthene and pyrene displayed the highest specificity. However, when the applicability of the six markers was tested on air samples from iron foundries, only naphthalene and pyrene were useful as markers for the carcinogenic compounds...

  4. Suspended particulate matter collection methods influence the quantification of polycyclic aromatic compounds in the river system.

    Science.gov (United States)

    Abuhelou, Fayez; Mansuy-Huault, Laurence; Lorgeoux, Catherine; Catteloin, Delphine; Collin, Valéry; Bauer, Allan; Kanbar, Hussein Jaafar; Gley, Renaud; Manceau, Luc; Thomas, Fabien; Montargès-Pelletier, Emmanuelle

    2017-08-16

    In this study, we compared the influence of two different collection methods, filtration (FT) and continuous flow field centrifugation (CFC), on the concentration and the distribution of polycyclic aromatic compounds (PACs) in suspended particulate matter (SPM) occurring in river waters. SPM samples were collected simultaneously with FT and CFC from a river during six sampling campaigns over 2 years, covering different hydrological contexts. SPM samples were analyzed to determine the concentration of PACs including 16 polycyclic aromatic hydrocarbons (PAHs), 11 oxygenated PACs (O-PACs), and 5 nitrogen PACs (N-PACs). Results showed significant differences between the two separation methods. In half of the sampling campaigns, PAC concentrations differed from a factor 2 to 30 comparing FT and CFC-collected SPMs. The PAC distributions were also affected by the separation method. FT-collected SPM were enriched in 2-3 ring PACs whereas CFC-collected SPM had PAC distributions dominated by medium to high molecular weight compounds typical of combustion processes. This could be explained by distinct cut-off threshold of the two separation methods and strongly suggested the retention of colloidal and/or fine matter on glass-fiber filters particularly enriched in low molecular PACs. These differences between FT and CFC were not systematic but rather enhanced by high water flow rates.

  5. Source apportionment and toxicity of atmospheric polycyclic aromatic hydrocarbons by PMF: Quantifying the influence of coal usage in Taiyuan, China

    Science.gov (United States)

    Yan, Yulong; He, Qiusheng; Guo, Lili; Li, Hongyan; Zhang, Hefeng; Shao, Min; Wang, Yuhang

    2017-09-01

    Atmospheric polycyclic aromatic hydrocarbons (PAHs) were analyzed in the gas phase and total suspended particulate (TSP) from summer 2014 to spring 2015 in Taiyuan, northern China. Taiyuan is an area with some of the highest atmospheric PAH levels in the world, and the total PAHs was highest in winter, followed by autumn, spring and summer. Low air temperature and a southern wind with low speed often led to higher PAH levels in Taiyuan. Although less than a half fraction, the benzo[a]pyrene equivalent concentration (BEQ) of particulate PAHs was almost equal to that of the total PAHs. Four sources, coal combustion, vehicle emissions, coke processing and biomass burning, were determined by positive matrix factorization (PMF), with contributions of 41.36%, 24.74%, 19.71% and 14.18% to the total PAHs in Taiyuan, respectively. Compared with the total PAHs, the particulate PAH solution underestimated the contribution of the coke processing, especially in winter, and overestimated vehicle emissions. The coke processing had a greater contribution to atmospheric PAHs with a southern wind at low speeds in winter in Taiyuan. Ultimately, the coke plants distributed in the Taiyuan-Linfen-Yuncheng basin should receive greater attention for air quality improvement in Taiyuan.

  6. 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

  7. 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

  8. A simple, comprehensive, and miniaturized solvent extraction method for determination of particulate-phase polycyclic aromatic compounds in air.

    Science.gov (United States)

    Santos, Aldenor G; Regis, Ana Carla D; da Rocha, Gisele O; Bezerra, Marcos de A; de Jesus, Robson M; de Andrade, Jailson B

    2016-02-26

    The method allowed simultaneous characterization of PAHs, nitro-PAHs and quinones in atmospheric particulate matter. This method employs a miniaturized micro-extraction step that uses 500 μL of an acetonitrile-dichloromethane mix and instrumental analysis by means of a high-resolution GC-MS. The method was validated using the SRM1649b NIST standard reference material as well as deuterated internal standards. The results are in good agreement with the certified values and show recoveries between 75% and 145%. Limit of detection (LOD) values for PAHs were found to be between 0.5 pg (benzo[a]pyrene) to 2.1 pg (dibenzo[a,h]anthracene), for nitro-PAHs ranged between 3.2 pg (1-nitrobenzo[e]pyrene) and 22.2 pg (3-nitrophenanthrene), and for quinones ranged between 11.5 pg (1,4-naphthoquinone) and 458 pg (9,10-phenanthraquinone). The validated method was applied to real PM10 samples collected on quartz fiber filters. Concentrations in the PM10 samples ranged from 0.06 to 15 ng m(-3) for PAHs, frompolycyclic aromatic compounds in airborne particles from both polluted and non-polluted atmospheres. Copyright © 2016 Elsevier B.V. All rights reserved.

  9. 20 Elemental Composition and Sources of Atmospheric Particulate ...

    African Journals Online (AJOL)

    `123456789jkl''''#

    the most environmental concerns in urban areas, especially in view of the adverse health effects associated with ambient atmospheric particles (Pope, 2000). In the urban environment, particulate matter may be generated among others by automotive vehicles (road dust), manufacturing processes, fossil fuel combustion ...

  10. An assessment of common atmospheric particulate matter sampling ...

    African Journals Online (AJOL)

    In this study, the atmospheric particulate matter (PM) was sampled using the tapered element oscillating microbalance, and the inductively coupled plasma mass spectroscopy (ICP-MS) and scanning electron microscopy coupled with energy dispersive spectrometry (SEM/EDS) were used for determination of elemental ...

  11. The study of polycyclic aromatic hydrocarbons in particulate fractions emitted by office printers and copiers

    Directory of Open Access Journals (Sweden)

    Małgorzata Szewczyńska

    2014-12-01

    Full Text Available Background: This article presents the study of polycyclic aromatic hydrocarbons (PAHs adsorbed on fine particles emitted during the simulated operation of office printers and copiers. Material and Methods: In the study three types of printers, and four types of office copiers were used. Measurements were carried out in a closed measuring chamber. Air samples (fractions of particulate matter, PM10 and PM2.5 were collected on Teflon filters. The analysis of PAHs was carried out according HPLC/FL. Results: The results of qualitative analysis of filters from PM2.5 and PM10 type samplers indicated the presence of the majority (10–14 of PAH congeners. The highest concentration of total PAHs was determined in the PM10 fraction in the air during the operation of a copier, and amounted to 36.52 μg×g–1. The total content of PAHs as determined in the fraction of fine particulates, size of < 2.5 μm, accounts for 48–84% of the PAH content in the < 10 μm fraction for printers and 63–89% for copiers. During the operation of both printers and copiers, benzo(apirene (BaP was identified in both fractions, PM2.5 and PM10. The maximum concentration of BaP in the fraction of < 10 μm particles emitted by a printer amounted to 3.29±0.2 μg×g–1. Conclusions: The studies showed that the composition of emitted substances and fine particles depends on the type of equipment and technology used. Fine particles emitted to the environment and organic compounds, including PAHs adsorbed on them may pose a threat to people working in such an environment. Med Pr 2014;65(6:733–741

  12. 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.

  13. 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

  14. 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. Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.

  15. Characteristics, sources, and cytotoxicity of atmospheric polycyclic aromatic hydrocarbons in urban roadside areas of Hangzhou, China.

    Science.gov (United States)

    Bai, Hongzhen; Zhang, Hongjian

    2017-03-21

    The primary objective of this study is to understand the profiles, sources and cytotoxic effects of atmospheric polycyclic aromatic hydrocarbons (PAHs), which are closely related to urban air contamination and public health, in urban roadside environments. On-road sampling campaigns were conducted from 2014 to 2015 at three urban road sites in Hangzhou, China. Sixteen gaseous and particulate matter (PM) 2.5-bound PAHs were identified and quantified using gas chromatography-mass spectrometry (GC-MS). The total PAH concentrations at the three sites ranged from 750 to1142 ng/m(3) and 1050 to 1483 ng/m(3) in summer and winter, respectively. Low molecular weight PAHs were the most abundant compounds (77-86%) and primarily existed in gas phase. The concentrations and phase distributions of high molecular weight PAHs were varied at three sites due to the differences in traffic volume, vehicle composition, engine loading, and nearby artificial activity. Diagnostic ratios of the principal mass (m/z,178, 202, 228 and 276) parent PAHs were statistically described to determine the PAH sources to urban roadsides; principal component analysis (PCA) was applied to apportion the sources. The results indicated that high- and low-temperature fuel processes, as well as residential and industrial emissions, were major contributors to roadside PAHs. The cytotoxic potential of the roadside PAHs was evaluated using a human epithelial lung cell line (A549). Cell viability was measured after a direct exposure to PAH extract. The results reflected the profiles of roadside PAHs at the three sites. The cytotoxicity of reference PAHs was evaluated to provide further insights into the cytotoxic potential of PAHs. We found that low molecular weight PAHs, which are less cytotoxic compounds, synergistically promoted the lethal effect of cytotoxic compounds, posing a potential threat to public health.

  16. Association of atmospheric concentrations of polycyclic aromatic hydrocarbons with their urinary metabolites in children and adolescents.

    Science.gov (United States)

    Poursafa, Parinaz; Amin, Mohammad Mehdi; Hajizadeh, Yaghoub; Mansourian, Marjan; Pourzamani, Hamidreza; Ebrahim, Karim; Sadeghian, Babak; Kelishadi, Roya

    2017-07-01

    This study aims to determine the atmospheric concentrations of particulate matter 2.5 (PM2.5)-bounded polycyclic aromatic hydrocarbons (PAHs) and their association with their urinary metabolites in children and adolescents. This study was conducted from October 2014 to March 2016 in Isfahan, Iran. We measured 16 species of PAHs bounded to PM2.5 by gas chromatography mass spectrometry (GC/MS) from 7 parts of the city. Moreover, PAH urinary metabolites were measured in 186 children and adolescents, randomly selected from households. Urinary metabolites consisted of 1-hydroxy naphthalene (1-naphthol), 2-hydroxy naphthalene (2-naphthol), 9-hydroxy phenanthrene (9-phenanthrol), and 1-hydroxy pyrene using GC/MS. Considering the short half-lives of PAHs, we measured the metabolites twice with 4 to 6 months of time interval. We found that the ambient concentrations of PAHs were significantly associated with their urinary metabolites. 1-hydroxy naphthalene and 2-hydroxy naphthalene concentrations showed an increase of 1.049 (95% CI: 1.030, 1.069) and 1.047 (95% CI: 1.025, 1.066) for each unit increase (1 ng/m3) in ambient naphthalene. Similarly, 1-hydroxy pyrene showed an increase of 1.009 (95% CI: 1.006-1.011) for each unit increase (1 ng/m3) in ambient pyrene concentration after adjustment for body mass index, physical activity level, urinary creatinine, age, and sex. The association of urinary 9-hydroxyphenanthrene and ambient phenantherene was significant in the crude model; however after adjustment for the abovementioned covariates, it was no more significant. We found significant correlations between exposure to ambient PM2.5-bounded PAHs and their urinary excretion. Considering the adverse health effects of PAHs in the pediatric age group, biomonitoring of PAHs should be underscored; preventive measures need to be intensified.

  17. Emission factors of particulate matter, polycyclic aromatic hydrocarbons, and levoglucosan from wood combustion in south-central Chile.

    Science.gov (United States)

    Jimenez, Jorge; Farias, Oscar; Quiroz, Roberto; Yañez, Jorge

    2017-07-01

    In south-central Chile, wood stoves have been identified as an important source of air pollution in populated areas. Eucalyptus (Eucalyptus globulus), Chilean oak (Nothofagus oblique), and mimosa (Acacia dealbata) were burned in a single-chamber slow-combustion wood stove at a controlled testing facility located at the University of Concepción, Chile. In each experiment, 2.7-3.1 kg of firewood were combusted while continuously monitoring temperature, exhaust gases, burn rate, and collecting particulate matter samples in Teflon filters under isokinetic conditions for polycyclic aromatic hydrocarbon and levoglucosan analyses. Mean particulate matter emission factors were 2.03, 4.06, and 3.84 g/kg dry wood for eucalyptus, oak, and mimosa, respectively. The emission factors were inversely correlated with combustion efficiency. The mean emission factors of the sums of 12 polycyclic aromatic hydrocarbons in particle phases were 1472.5, 2134.0, and 747.5 μg/kg for eucalyptus, oak, and mimosa, respectively. Fluoranthene, pyrene, benzo[a]anthracene, and chrysene were present in the particle phase in higher proportions compared with other polycyclic aromatic hydrocarbons that were analyzed. Mean levoglucosan emission factors were 854.9, 202.3, and 328.0 mg/kg for eucalyptus, oak, and mimosa, respectively. Since the emissions of particulate matter and other pollutants were inversely correlated with combustion efficiency, implementing more efficient technologies would help to reduce air pollutant emissions from wood combustion. Residential wood burning has been identified as a significant source of air pollution in populated areas. Local wood species are combusted for home cooking and heating, which releases several toxic air pollutants, including particulate matter, carbon monoxide, and polycyclic aromatic hydrocarbons. Air pollutant emissions depend on the type of wood and the technology and operational conditions of the wood stove. A better understanding of emissions from

  18. 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.

  19. 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%).

  20. Heterogeneous Reactions of Polycyclic Aromatic Hydrocarbons on Atmospheric and Terrestrial Surfaces

    Science.gov (United States)

    Simonich, S. L.

    2014-12-01

    The heterogeneous reactions of five higher molecular weight polycyclic aromatic hydrocarbons (PAHs), benzo[a]pyrene-d12 (BaP-d12), benzo(k)fluoranthene-d12 (BkF-d12), benzo[g,h,i]perylene-d12 (BghiP-d12), dibenzo(a,i)pyrene-d14 (DBaiP-d14), and dibenzo[a,l]pyrene (DalP), with NO2, NO3/N2O5, O3, and OH radicals were investigated in a 7000 L indoor Teflon chamber. Quartz fiber filters (QFF) were used as the reaction surface and substrate and the analyses of parent PAHs and Nitro-PAH (NPAH) products was conducted using electron impact gas chromatographic mass spectrometry (GC/MS) and negative chemical ionization GC/MS. In parallel to the laboratory experiments, a theoretical study was conducted to assist in determining the formation of NPAH isomers based on the OH-radical initiated reaction. The thermodynamic stability of OH-PAH intermediates was used to indicate the position of highest electron density and the most stable NPAH products were synthesized to confirm their identity. NO2 and NO3/N2O5 were the most effective oxidizing agents in transforming PAHs deposited on filters to NPAHs, under the experimental conditions. Reaction of BaP-d12, BkF-d12 and BghiP-d12 resulted in the formation of several mono-nitro PAH isomer product, while the reaction of DalP and DaiP-d14 resulted in the formation of only one mono-nitro PAH isomer product. The direct-acting mutagenicity of the products increased the most after NO3/N2O5 exposure, particularly for BkF-d12 in which the formation of dinitro- PAHs was observed. In addition, the degradation of particulate matter (PM)-bound PAHs by heterogeneous reaction with OH radicals, O3, NO3/N2O5 was also studied. Ambient PM samples collected from Beijing, China and Riverside, California were exposed in an indoor chamber under simulated trans-Pacific atmospheric transport conditions and the formation of NPAHs was studied. NPAHs were most effectively formed during the NO3/N2O5 exposure and, for all exposures, there was no significant

  1. Sanitary impact of the particulate atmospheric urban pollution; Impact sanitaire de la pollution atmospherique urbaine particulaire

    Energy Technology Data Exchange (ETDEWEB)

    Sentissi, M.

    1999-03-22

    The pollution of particulates origin is one of the principle actual problem relative to air quality. In France, the fine particulates come from industry and automobile traffic, especially, the diesel vehicles. The most worrying characteristic is their fineness, that allow them to stay in suspension during a long time and penetrate into pulmonary alveoli, with toxic elements at their surface such metals, acids, polycyclic aromatic hydrocarbons. The objective of this work is to take stock of epidemiology and toxicology studies evaluating the sanitary impact of particulates in suspension. (N.C.)

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

    Directory of Open Access Journals (Sweden)

    A. F. Longo

    2016-10-01

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

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

    Science.gov (United States)

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

    2016-10-01

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

  4. 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.

  5. 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.

  6. Atmospheric bulk deposition of polycyclic aromatic hydrocarbons in Shanghai: Temporal and spatial variation, and global comparison.

    Science.gov (United States)

    Feng, Daolun; Liu, Ying; Gao, Yi; Zhou, Jinxing; Zheng, Lirong; Qiao, Gang; Ma, Liming; Lin, Zhifen; Grathwohl, Peter

    2017-11-01

    Atmospheric deposition leads to accumulation of atmospheric polycyclic aromatic hydrocarbons (PAHs) on urban surfaces and topsoils. To capture the inherent variability of atmospheric deposition of PAHs in Shanghai's urban agglomeration, 85 atmospheric bulk deposition samples and 7 surface soil samples were collected from seven sampling locations during 2012-2014. Total fluxes of 17 PAHs were 587-32,300 ng m -2 day -1 , with a geometric mean of 2600 ng m -2 day -1 . The deposition fluxes were categorized as moderate to high on a global scale. Phenanthrene, fluoranthene and pyrene were major contributors. The spatial distribution of deposition fluxes revealed the influence of urbanization/industrialization and the relevance of local emissions. Meteorological conditions and more heating demand in cold season lead to a significant increase of deposition rates. Atmospheric deposition is the principal pathway of PAHs input to topsoils and the annual deposition load in Shanghai amounts to ∼4.5 tons (0.7 kg km -2 ) with a range of 2.5-10 tons (0.4-1.6 kg km -2 ). Copyright © 2017 Elsevier Ltd. All rights reserved.

  7. Atmospheric concentrations of particulate phase of PAHs and their ...

    African Journals Online (AJOL)

    The Niger Delta Region of Nigeria is witnessing increase in petroleum exploration activities. Natural Crude oil deposits contain significant amounts of Polycyclic Aromatic Hydrocarbons (PAHs) arising from chemical conversion of natural product molecules. The EPA (2002) has classified seven PAH compounds as probable ...

  8. Indoor/outdoor relationship of trace metals in the atmospheric particulate matter of an industrial area

    Science.gov (United States)

    Nazir, Rashida; Shaheen, Nazia; Shah, Munir H.

    2011-08-01

    Present study is based on the measurement and monitoring of indoor and outdoor atmospheric particulate matter from an industrial area (Wah Cantt, Pakistan). The particulate samples are collected on glass fiber filter paper using high volume air sampler. Trace metals (Cd, Co, Cr, Cu, Fe, Mn, Pb, Sb and Zn) in the particulate samples are estimated by atomic absorption spectrometry. On the average TSP level is significantly higher in outdoor atmosphere than indoor, and both of them are higher than WHO and USEPA standards. The distribution of trace metals is considerably diverse in indoor and outdoor particulates. Average concentrations of Fe, Zn, Co, Cr and Mn are significantly higher in outdoor particulates, whereas Cu and Pb levels are considerably higher in the indoor particulates. Source apportionment carried out by PCA and CA is diverse in indoor/outdoor particulates and the major pollution sources identified are industrial activities, automobile emissions and soil derived dust. Among the trace metals, Cd, Sb, Zn, Pb and Co are found to be highly enriched in the atmospheric particulate matter. The present atmospheric trace metals levels are also compared with those reported from other regions around the world, and are many-folds higher than previously reported results.

  9. 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.

  10. Chemical Characterization of Atmospheric Particulate Matter from Prudhoe Bay, Alaska

    Science.gov (United States)

    Gunsch, M.; Kirpes, R.; Moffett, C. E.; Sheesley, R. J.; Pratt, K.

    2016-12-01

    Climate change is impacting the Arctic, leading to increasing temperatures and decreasing summer sea ice coverage which has allowed for increased oil and gas extraction activities. Prudhoe Bay is currently the second highest source of particulate matter from oil and gas extraction in the Arctic, and 3rd largest oil field in the United States. With drilling operations expected to increase due to the reduced sea ice coverage, these emissions, specifically contributions from black carbon and organic carbon, are expected to continue to increase over the coming decades. Given the complexity and evolving nature of atmospheric particles, as well as the logistical challenges associated with Arctic measurements, many uncertainties remain in our understanding of the impacts of increasing emissions in the Arctic. To investigate the size and chemistry of individual particles emitted from activities within the Prudhoe Bay oil fields in real-time, an aerosol time-of-flight mass spectrometer (ATOFMS) was deployed 300 km northwest of Prudhoe Bay to Barrow, AK during August-September 2015 as well as inside the Prudhoe Bay oil fields at Oliktok Point, AK during August-September 2016. During the 2015 measurements, particle number concentrations increased 10 times when under the influence of Prudhoe Bay, primarily from sub-50 nm particles attributed to transported combustion emissions. ATOFMS also identified increased number fractions of soot and organic carbon-sulfate particles (0.2 - 1.5 μm in diameter) when comparing Prudhoe Bay influential periods to Arctic Ocean influential periods. During 2016 measurements, parallel size-resolved number concentration measurements allowed for near-source quantification of number and mass concentrations of particles from the various sources of combustion within the oil fields, including residual fuel, diesel fuel and biomass burning. These measurements represent the first single particle chemical characterization of oil and gas extraction

  11. 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...

  12. Effects of oil pipeline explosion on ambient particulate matter and their associated polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Zhao, Yue; Cao, Lixin; Zhou, Qing; Que, Qiming

    2015-01-01

    Effects of the oil pipeline explosion on PM(2.5)-associated polycyclic aromatic hydrocarbons (PAHs) and their substituted (alkylated, nitrated, oxygenated, hydroxyl and chlorinated) derivatives are assessed near the accident scene of Qingdao, China. Compared with those in TSP-PM(2.5), gaseous phase, burn residue and unburned crude oil, eighty-nine PAHs in PM(2.5) are identified and quantified to investigate the composition, temporal and spatial distribution, and sources. The concentrations of PM(2.5)-associated parent PAHs increase approximately seven times from the non-explosion samples to the explosion samples (mean ± standard deviation: 112 ± 2 vs 764 ± 15 ng/m(3)), while some substituted products (nitro- and oxy-) increase by two orders of magnitude (3117 ± 156 pg/m(3) vs 740 ± 37 ng/m(3)). The toxicity evaluation indicates the BaP equivalent concentrations (based on the US EPA's toxicity factors) in PM(2.5) are much higher than those in the other phases, especially for a long duration after the tragic accident.

  13. 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

  14. Atmospheric oxidative chemistry of organic particulate emissions from fuel combustion.

    Science.gov (United States)

    2011-03-25

    "Construction and characterization of the University of Vermont Environmental Chamber (UVMEC) : were completed in this last phase of the project. The primary function of the UVMEC is to enable : tropospheric particulate formation and aging studies to...

  15. Pollution characteristics, sources and lung cancer risk of atmospheric polycyclic aromatic hydrocarbons in a new urban district of Nanjing, China.

    Science.gov (United States)

    Wang, Tao; Xia, Zhonghuan; Wu, Minmin; Zhang, Qianqian; Sun, Shiqi; Yin, Jing; Zhou, Yanchi; Yang, Hao

    2017-05-01

    This paper focused on the pollution characteristics, sources and lung cancer risk of atmospheric polycyclic aromatic hydrocarbons (PAHs) in a new urban district of Nanjing, China. Gaseous and aerosol PM2.5 (particulate matter with aerodynamic diameter smaller than 2.5μm) samples were collected in spring of 2015. Sixteen PAHs were extracted and analyzed after sampling. Firstly, arithmetic mean concentrations of PAHs and BaPeq (benzo[a]pyrene equivalent) were calculated. The mean concentrations of PAHs were 29.26±14.13, 18.14±5.37 and 48.47±16.03ng/m3 in gas phase, particle phase and both phases, respectively. The mean concentrations of BaPeq were 0.87±0.51, 2.71±2.17 and 4.06±2.31ng/m3 in gas phase, particle phase and both phases, respectively. Secondly, diagnostic ratios and principal component analysis were adopted to identify the sources of PAHs and the outcomes were the same: traffic exhaust was the predominant source followed by fuel combustion and industrial process. Finally, incremental lung cancer risk (ILCR) induced by whole year inhalation exposure to PAHs for population groups of different age and gender were estimated based on a Monte Carlo simulation. ILCR values caused by particle phase PAHs were greater than those caused by gas phase PAHs. ILCR values for adults were greater than those for other age groups. ILCR values caused by total (gas+particle) PAHs for diverse groups were all greater than the significant level (l0-6), indicating high potential lung cancer risk. Sensitivity analysis results showed that cancer slope factor for BaP inhalation exposure and BaPeq concentration had greater impact than body weight and inhalation rate on the ILCR. Copyright © 2016. Published by Elsevier B.V.

  16. Analysis of polycyclic aromatic hydrocarbons adsorbed on particles of atmospheric interest using pressurised fluid extraction

    Energy Technology Data Exchange (ETDEWEB)

    Perraudin, Emilie [Universite Bordeaux I, Laboratoire de Physico et Toxico-Chimie des Systemes Naturels, UMR 5472 CNRS, Talence Cedex (France); Universite Bordeaux I, Laboratoire de Physico-Chimie Moleculaire, UMR 5803 CNRS, Talence Cedex (France); Budzinski, Helene [Universite Bordeaux I, Laboratoire de Physico et Toxico-Chimie des Systemes Naturels, UMR 5472 CNRS, Talence Cedex (France); Villenave, Eric [Universite Bordeaux I, Laboratoire de Physico-Chimie Moleculaire, UMR 5803 CNRS, Talence Cedex (France)

    2005-09-01

    Pressurised fluid extraction (PFE) was used for the measurement of 13 polycyclic aromatic hydrocarbons (PAHs) adsorbed on different types of particles: two model particles (PAH-coated silica, PAH-coated graphite) and two natural atmospheric particles (urban dust and diesel exhaust, from NIST reference materials). Samples were analysed by gas chromatography coupled to mass spectrometry. Extraction efficiency was evaluated with internal standard recovery yields and was shown to depend on the nature of the particle, on the structure of the analytes and on the PAH concentration. Extraction conditions (toluene, 130 C, 130 bar, 2 x 8-min static cycles) were optimised to extract PAHs when strongly interacting with solid matrices and were validated by the analysis of two PAH-certified materials. (orig.)

  17. Polycyclic Aromatic Hydrocarbons (PAHs in the atmosphere of the Baltic Sea Region

    Directory of Open Access Journals (Sweden)

    Julia Gaffke

    2016-03-01

    Full Text Available The paper presents a review of publications on the concentrations of polycyclic aromatic hydrocarbons in the atmosphere of the Baltic Sea Region (BSR. It indicates the main emission sources of these substances, related to anthropogenic activity. These include incomplete combustion of fuels in engines on land and from marine transportation, as well as the burning of coal in the community sector. High PAH concentrations in the air are also related to increased industrial activity in urban areas. In the Baltic Sea Region, Germany and Poland have been determined to be responsible for the greatest proportion of PAH emissions. However, the highest number of exceedances of the accepted annual norm for benzo(apyrene concentrations was recorded in Poland.

  18. Polycyclic aromatic hydrocarbons (PAHs) in atmospheric dustfall from the industrial corridor in Hubei Province, Central China.

    Science.gov (United States)

    Zhang, Jiaquan; Qu, Chengkai; Qi, Shihua; Cao, Junji; Zhan, Changlin; Xing, Xinli; Xiao, Yulun; Zheng, Jingru; Xiao, Wensheng

    2015-10-01

    Thirty atmospheric dustfall samples collected from an industrial corridor in Hubei Province, central China, were analyzed for 16 USEPA priority polycyclic aromatic hydrocarbons (PAHs) to investigate their concentrations, spatial distributions, sources, and health risks. Total PAH concentrations (ΣPAHs) ranged from 1.72 to 13.17 µg/g and averaged 4.91 µg/g. High molecular weight (4-5 rings) PAHs averaged 59.67% of the ΣPAHs. Individual PAH concentrations were not significantly correlated with total organic carbon, possibly due to the semi-continuous inputs from anthropogenic sources. Source identification studies suggest that the PAHs were mainly from motor vehicles and biomass/coal combustion. The incremental lifetime cancer risks associated with exposure to PAHs in the dustfall ranged from 10(-4) to 10(-6); these indicate potentially serious carcinogenic risks for exposed populations in the industrial corridor.

  19. Evaluation of airborne respirable particulate matter and polycyclic aromatic hydrocarbon exposure of asphalt workers

    Directory of Open Access Journals (Sweden)

    Teresa Cirillo

    2007-12-01

    Full Text Available

    Introduction: Assessment of exposure to the airborne respirable particles (PM10 and polycyclic aromatic hydrocarbons (PAHs of asphalt manufacturing and road paving workers in the Campania region (Italy.

    Materials and Methods: A study was carried out during 2006 and involved 5 firms producing and employing bitumen in road paving activities. The workers studied were categorized on the basis of their job as workers in bitumen manufacturing, in road paving and in workers not exposed at bitumen fume considered like controls.

    Results: In the manufacturing plants the average concentrations of airborne PM10 were 1125±445 ìg/m3 in the HMA manufacturing workers’ areas; 314±81 ìg/m3 in the process surveyors’ cabins and 92±27 ìg/m3 in the controls’ areas (administrative offices. Within the breathing zones of the worker, the average PAHs levels in air were as follows: 367±198 ng/m3 for HMA manufacturing workers; 348±172 ng/m3 for process surveyors; 21±2 ng/m3 for the controls. At the road paving sites the average airborne PM10 levels were 1435±325 ìg/m3 for roller operators; 1610±356 ìg/m3 for paver operators; 319±108 ìg/m for the controls (traffic controllers. PAHs in the breathing zones were 1220±694 ng/m3 for the paver operators; 1360±575 ng/m3 for the roller operators’ and 139±135 ng/m3 for the traffic controllers’. The results show that the more consistent hazard for asphalt workers’ health is derived from exposure to airborne PM10 both in exposed and in non-exposed (controls workers.

  20. Atmospheric polycyclic aromatic hydrocarbons (PAHs) of southern Taiwan in relation to monsoons.

    Science.gov (United States)

    Cheng, Jing-O; Ko, Fung-Chi; Lee, Chon-Lin; Fang, Meng-Der

    2016-08-01

    The concentrations and gas-particle partitioning of atmospheric polycyclic aromatic hydrocarbons (PAHs) were intensively measured in the Hengchun Peninsula of southern Taiwan. The concentrations of total PAH (Σ38PAH), including gas and particle phases, ranged from 0.85 to 4.40 ng m(-3). No significant differences in the PAH levels and patterns were found between the samples taken at day and at night. The gas phase PAH concentrations were constant year-round, but the highest levels of particle-associated PAHs were found during the northeast monsoon season. Long-range transport and rainfall scavenging mechanisms contributed to the elevated levels in aerosols andΣ38PAH concentrations. Results from principal component analysis (PCA) indicated that the major sources of PAHs in this study were vehicular emissions. The back trajectories demonstrated that air mass movement driven by the monsoon system was the main influence on atmospheric PAH profiles and concentrations in the rural region of southern Taiwan. Gas-particle partition coefficients (K p ) of PAHs were well-correlated with sub-cooled liquid vapor pressures (P (o) L ) and demonstrated significant seasonal variation between the northeast (NE) and the southwest (SW) monsoon seasons. This study sheds light on the role of Asian monsoons regarding the atmospheric transport of PAHs.

  1. 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

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

    Energy Technology Data Exchange (ETDEWEB)

    Forbes, Patricia B.C., E-mail: pforbes@csir.co.z [Natural Resources and the Environment, Council for Scientific and Industrial Research, PO Box 395, Pretoria 0001 (South Africa); Department of Chemistry, Faculty of Natural Science, University of Pretoria, Pretoria 0002 (South Africa); Rohwer, Egmont R., E-mail: egmont.rohwer@up.ac.z [Department of Chemistry, Faculty of Natural Science, University of Pretoria, Pretoria 0002 (South Africa)

    2009-08-15

    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 (<5 min), cost effective analysis of samples. Those yielding interesting results could be further analysed by direct thermal desorption-gas chromatography-mass spectrometry (TD-GC-MS, with limits of detection of approx0.3 ng m{sup -3}), as photodegradation was minimal (<10% over 5 min irradiation). Small amounts of naphthalene photodegradation products identified by TD-GC-MS after >15 min irradiation, included phenol, benzyl alcohol and phthalic anhydride. Without any signal optimization, a LIF detection limit of approx1 mug m{sup -3} was established for naphthalene using a diffusion tube (diffusion rate of 2 ng s{sup -1}) and 292 nm excitation. - A novel method for rapid analysis of atmospheric PAHs by laser induced fluorescence allows for more detailed trend determinations.

  3. Atmospheric deposition of polycyclic aromatic hydrocarbons near New England coastal waters

    Science.gov (United States)

    Golomb, D.; Barry, E.; Fisher, G.; Varanusupakul, P.; Koleda, M.; Rooney, T.

    Wet and dry deposition of polycyclic aromatic hydrocarbons (PAHs) was measured at Nahant, Massachusetts, a peninsula jutting into Massachusetts Bay and Wolf Neck, a peninsula jutting into Casco Bay, Maine. Wet deposition (rain and snow) was collected in a funnel which drains into a shielded, temperature controlled receiving bottle. Dry deposition of gaseous and particulate PAHs was collected onto an exposed water surface. PAHs were analyzed by solid phase extraction and gas chromatography-mass spectrometry. Sixteen PAH species were analyzed, ranging from acenaphthylene to coronene. The mean wet deposition rate of the sum of the 16 species is 720 ng m -2 cm -1 precipitation at Nahant, and 831 ng m -2 cm -1 precipitation at Wolf Neck. Wet deposition is attributed to regional PAH emitting sources. Storm patterns appear to bring somewhat higher wet deposition of PAHs to Wolf Neck than to Nahant. The mean dry deposition rate is 95 ng m -2 h -1 at Nahant and 9.3 ng m -2 h -1 at Wolf Neck. The large difference is attributed to the fact that Nahant is close to the urban-industrial metropolitan Boston area and Logan International Airport, whereas Wolf Neck has no major PAH-emitting sources nearby. Individual measurements have an error bracket of ±30%. The Chemical Mass Balance model was used to apportion the dry deposition to source categories. At Nahant, nine samples gave valid statistical attributes with a mean apportionment: jet exhaust 35%, gasoline fueled vehicles 32%, diesel fueled vehicles 17%, wood combustion 13%, others 3%. At Wolf Neck, six samples yielded a mean apportionment: jet exhaust 30%, gasoline vehicles 28%, diesel vehicles 18%, wood combustion 16%, others 8%. There is a considerable variation between the samples. The apportionment is greatly dependent on the quality and selection of the model inputs, i.e. source signatures, which for PAHs are questionable.

  4. Polycyclic aromatic hydrocarbons in occupational vs. urban environmental air

    NARCIS (Netherlands)

    Branisteanu, R.; Aiking, H.

    1998-01-01

    Objectives: To evaluate the balance between occupational and environmental exposure to suspended particulate matter (SPM) and polycyclic aromatic hydrocarbons (PAHs), comparison measurements were performed in a coal-fired power plant and the urban atmosphere from the town nearby. Methods: The

  5. The variation of atmospheric particulate matter concentration in the suburb areas over Fuzhou city

    Science.gov (United States)

    Fu, Weicong; Chen, Ziru; Zhu, Zhipeng; Huang, Shuping; Dong, Jianwen; Ding, Guochang

    2017-05-01

    The atmospheric particulate matter concentration (APMC) and meteorological factor were supervised and analyze the variation and characteristics in Fuzhou National Forest Park. The result showed that: 1) the atmospheric particulate matter concentration is generally low in summer and high in winter, while in spring and autumn, the APMC with different diameters changed between summer and winter. 2) The daily variation of APMC in different seasons has different characteristics; 3) maximum wind speed, average wind speed, air pressure, wet bulb index, thermal index, humidity and temperature were the meteorological factors that affect APMC. Improving the site condition play a positive role on reducing the APMC and enhancing environmental functions.

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

    Science.gov (United States)

    Poulain, L.; Iinuma, Y.; Müller, K.; Birmili, W.; Weinhold, K.; Brüggemann, E.; Gnauk, T.; Hausmann, A.; Löschau, G.; Wiedensohler, A.; Herrmann, H.

    2011-04-01

    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 contribution of residential wood

  7. 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.

  8. 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.

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

    Science.gov (United States)

    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 is 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 microm particle diameter, indicating that Pb is mainly concentrated in fine fraction. Lead in the fine fraction is enriched by a factor of 10(3)-10(4) 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.

  10. Modeling of nitro-polycyclic aromatic hydrocarbon formation and decay in the atmosphere

    Science.gov (United States)

    Fan, Zhihua; Chen, Danhua; Birla, Parag; Kamens, Richard M.

    A reaction mechanism of polycyclic aromatic hydrocarbons (PAH) and nitro-PAH (NPAH) in the gas and particle phase in the atmosphere has been further evaluated and modified using outdoor smog chamber experimental results. Diesel exhaust emissions were added to a 190 m 3 outdoor smog chamber and permitted to age under conditions of daylight and darkness. A sampling train consisting of an annular denuder, filter, and polyurethane foam (PUF) or XAD resin was used for the collection of gas and particle phase PAH and NPAH. On the basis of the results, the current denuder design has sufficient flow (20 ℓ min -1) and adsorption characteristics for collection of PAH and NPAH in the chamber studies. Outdoor smog chamber experiments with dilute diesel soot were conducted under different initial photochemical conditions. Ozone (0 3), nitrogen oxides (NO x), and volatile hydrocarbons in the gas phase were monitored. Simulations for fluoranthene (FL) and pyrene (PY) in the gas phase were close to chamber observations, but those for the particle behavior of FL and PY were not as good. This may occur because PAH and NPAH inside of the particle are not available for reaction in sunlight. Mono-nitro-pyrenes (NPYs) and nitro-fluoranthenes (NFLs) were almost exclusively found in particle associated extracts. This implied that no or non-detectable 2nitro-FL (2NF) or 2nitro-PY (2NP) distributed in the gas phase and that they deposited on particles immediately after formation in the gas phase by the photochemical processes. Formation of 2NF was observed in the chamber, but 2NP degraded rapidly under photochemical conditions. Reasonable simulation results were obtained for 2NP and 2NF. The addition of NO 2 to the gas phase adduct of FL + OH or PY + OH was the main reaction for NPAH formation. Photodecomposition was the main loss pathway for NPAH in the atmosphere.

  11. Photodynamic bioassay of polycyclic air pollutants

    Energy Technology Data Exchange (ETDEWEB)

    Epstein, S.S.; Small, M.; Koplan, J.; Mantel, N.; Falk, H.L.; Sawicki, E.

    1963-11-01

    Fifteen fractions of organic atmospheric particulates from several American cities were bioassayed for photodynamic activity using paramecium caudatum and results obtained were expressed as apparent potencies relative to an arbitrary benoz(a)pyrene standard. All six crude benzene extracts assayed showed photodynamic activity, with a correlation evident between apparent relative potencies as determined by bioassay, and benzo(a)pyrene concentrations as determined by chemical analysis. Five aliphatic fractions were photodynamically inactive. The single aromatic fraction tested had high activity. Three oxygenated fractions showed photodynamic activity, despite the absence from them of benzo(a)pyrene and other polycyclic hydrocarbons of known structure commonly found in atmospheric particulates. Such oxygenated fractions are reportedly carcinogenic. This pilot study suggests that photodynamic bioassay may provide a rapid, simple, and economical biological index of potential carcinogenic hazard attributable to polycyclic hydrocarbons. The utility of the assay for this purpose should be further evaluated. 14 references, 2 figures, 4 tables.

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

    Science.gov (United States)

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

    2017-04-01

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

  13. 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. Copyright © 2014 Elsevier Ltd. All rights reserved.

  14. Inferring Atmospheric Particulate Matter Concentrations from Chinese Social Media Data.

    Science.gov (United States)

    Tao, Zhu; Kokas, Aynne; Zhang, Rui; Cohan, Daniel S; Wallach, Dan

    2016-01-01

    Although studies have increasingly linked air pollution to specific health outcomes, less well understood is how public perceptions of air quality respond to changing pollutant levels. The growing availability of air pollution measurements and the proliferation of social media provide an opportunity to gauge public discussion of air quality conditions. In this paper, we consider particulate matter (PM) measurements from four Chinese megacities (Beijing, Shanghai, Guangzhou, and Chengdu) together with 112 million posts on Weibo (a popular Chinese microblogging system) from corresponding days in 2011-2013 to identify terms whose frequency was most correlated with PM levels. These correlations are used to construct an Air Discussion Index (ADI) for estimating daily PM based on the content of Weibo posts. In Beijing, the Chinese city with the most PM as measured by U.S. Embassy monitor stations, we found a strong correlation (R = 0.88) between the ADI and measured PM. In other Chinese cities with lower pollution levels, the correlation was weaker. Nonetheless, our results show that social media may be a useful proxy measurement for pollution, particularly when traditional measurement stations are unavailable, censored or misreported.

  15. Distortion of particulate extinction profiles measured with lidar in a two-component atmosphere.

    Science.gov (United States)

    Kovalev, V A; Moosmüller, H

    1994-09-20

    Distortions of particular extinction-coefficient profiles measured with lidar in a two-component (molecular and aerosol) scattering atmosphere are analyzed. The error of the extinction coefficient measured at range r depends on the location of the point r(b), where a boundary value is specified, and the particulate optical depth of the atmosphere between r and r(b); the particulate backscatter-to-extinction ratio; and the ratio of particulate and molecular scattering extinction. If the near-end solution is used, small measurement errors can produce a significant divergence between the actual and the retrieved extinction-coefficient profiles, even if the boundary value and the particulate backscatter-to-extinction ratio are specified accurately. This effect is exacerbated at small values of the particulate scattering coefficient and the backscatter-to-extinction ratio. When reasonable criteria are used, feasible minimum and maximum boundary values can be specified to restrict the range of lidar equation solutions from below and from above.

  16. Distribution of Polycyclic Aromatic Hydrocarbons between the Particulate and the Gas Phase of Mainstream Cigarette Smoke in Relation to Cigarette Technological Characteristics

    Directory of Open Access Journals (Sweden)

    Kalaitzoglou M

    2014-12-01

    Full Text Available Particulate- and gas-phase polycyclic aromatic hydrocarbons (PAHs were determined in the mainstream smoke (MSS of 59 manufactured cigarette brands (commercially available brands of unknown tobacco and blend type with variable ‘tar’ yields and physical/technological characteristics. Depending on the existence/absence of filter, the ‘tar’ yield indicated on the packet, and the cigarette length and diameter, the examined cigarette brands were classified into 15 groups: non filter (NF, high (H, medium (M, light (L, super light (SL, ultra light (UL, one-tar yields (O, 100 mm long cigarettes (H-100, L-100, SL-100, UL-100, O-100, and slim cigarettes (SL-SLIM, UL-SLIM, O-SLIM. Cigarettes were smoked in a reference smoking machine equipped with glass fibre filters for collection of PAHs bound to total particulate matter (TPM, and polyurethane foam plugs (PUF for collection of gas-phase PAHs. The relationships of gas- and particulate-phase concentrations of PAHs (ng/cig with the contents of typical MSS components, such as TPM, ‘tar’, nicotine and carbon monoxide were investigated. In addition, the phase partitioning of PAHs in MSS was evaluated in relation to the technological characteristics of cigarettes.

  17. Atmospheric Particulate Matter Pollution during the 2008 Beijing Olympics

    Science.gov (United States)

    WANG, WENTAO; PRIMBS, TOBY; TAO, SHU; ZHU, TONG; SIMONICH, STACI L. MASSEY

    2009-01-01

    Size fractionated particulate matter (PM) samples (including PM2.5 and PM10) were collected at Peking University in Northwestern Beijing, China for a 2 week period prior to the Olympics, during the 2 week period of the Olympics, and for a 4 week period following the 2008 Olympics, during both source control and non-source control period. PM10 concentrations in this study were high correlated with, but a factor of 1.3 times higher than, the Beijing Environmental Protection Bureau's PM10 concentrations at near-by sites because of differences in the measurement methods used. The mean PM2.5 and PM10 concentrations were statistically different, and lower by 31 and 35%, during the Olympic period compared to the non-Olympic period. However, the PM concentrations were not statistically different between the source control and non-source control periods. While meteorological parameters (air masses from the south and precipitation) accounted for 40% of the total variation in PM10 concentration, source control accounted for 16%, suggesting that meteorology accounted for more of the variation in PM concentration than source control measures. The PM10 concentrations in Beijing during the Olympic period were 2.9, 3.5, and 1.9 times higher than those in Atlanta, Sydney and Athens. In addition, the PM2.5 and PM10 concentrations during the Olympic period exceeded the WHO 24-hour guideline 100% and 81% of the time, respectively. Finally, the PM10 concentrations in October, November, and December 2008 were reduced by 9% to 27% compared to the same months in 2007, suggesting that the Olympic source control efforts (and possibly a down turn in the economy) have resulted in lower PM10 concentrations in Beijing. PMID:19708359

  18. 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.

  19. Impact of atmospheric deposition on particulate iron flux and distribution in northwestern Mediterranean waters

    Science.gov (United States)

    Quétel, Christophe R.; Remoudaki, Emmanouela; Davies, Joanne E.; Miquel, Juan-Carlos; Fowler, Scott W.; Lambert, Claude E.; Bergametti, Gilles; Buat-Ménard, Patrick

    1993-05-01

    Iron distribution can be significantly influenced b the interactions between atmospheric inputs and internal recycling within the water column. This question was investigated in the northwestern Mediterranean Sea as part of the French DYFAMED program. Sediment traps were moored at 80, 200 and 1000 m depth at 42°44'N, 8°31'E during 1986-1987 to collect settling particles in which iron was analysed. During the same sampling period, concurrent atmospheric deposition fluxes of iron were measured at Capo Cavallo, Corsica, 20 nautical from our marine sampling site. Some short but intense atmospheric inputs (1.5-2.4 mg m -2 day -1 during 5-20 consecutive days) of mineral matter from Africa are shown to be sufficient to explain the yearly particulate iron flux leaving surface waters at 200 m depth. Zooplanktonic grazing activity, particularly intense from April to June, is mostly responsible for the sedimentation of iron. Faecal pellets control the total iron flux because they incorporate both iron associated with aluminosilicates (refractory particulate iron) and most of iron associated with biological material (biogenic iron).There was anout 3300 ppm of iron in the organic matter collected by the sediment traps at 200 m during summer and fall. At 1000 m depth this concentration was greater by a factor of 2. During the same period, the calculated ratio of refractory particulate iron (Fe REFR) to particulate aluminium for the large particles at 80 and 200 m depth ((Fe REFRA1) TRAP = 0.43), was lower than the Fe/A1 ratio usually measured in the Saharan aerosol (0.5 < Fe/A1 < 0.7). This observation is underscored by the amplitude of the dissolved/particulate exchanges and suggests that most of the iron associated with sinking organic matter is provided by atmospheric input.

  20. Atmospheric ammonia and particulate inorganic nitrogen over the United States

    Directory of Open Access Journals (Sweden)

    C. L. Heald

    2012-11-01

    Full Text Available We use in situ observations from the Interagency Monitoring of PROtected Visual Environments (IMPROVE network, the Midwest Ammonia Monitoring Project, 11 surface site campaigns as well as Infrared Atmospheric Sounding Interferometer (IASI satellite measurements with the GEOS-Chem model to investigate inorganic aerosol loading and atmospheric ammonia concentrations over the United States. IASI observations suggest that current ammonia emissions are underestimated in California and in the springtime in the Midwest. In California this underestimate likely drives the underestimate in nitrate formation in the GEOS-Chem model. However in the remaining continental United States we find that the nitrate simulation is biased high (normalized mean bias > = 1.0 year-round, except in Spring (due to the underestimate in ammonia in this season. None of the uncertainties in precursor emissions, the uptake efficiency of N2O5 on aerosols, OH concentrations, the reaction rate for the formation of nitric acid, or the dry deposition velocity of nitric acid are able to explain this bias. We find that reducing nitric acid concentrations to 75% of their simulated values corrects the bias in nitrate (as well as ammonium in the US. However the mechanism for this potential reduction is unclear and may be a combination of errors in chemistry, deposition and sub-grid near-surface gradients. This "updated" simulation reproduces PM and ammonia loading and captures the strong seasonal and spatial gradients in gas-particle partitioning across the United States. We estimate that nitrogen makes up 15−35% of inorganic fine PM mass over the US, and that this fraction is likely to increase in the coming decade, both with decreases in sulfur emissions and increases in ammonia emissions.

  1. Assessing the inhalation cancer risk of particulate matter bound polycyclic aromatic hydrocarbons (PAHs) for the elderly in a retirement community of a mega city in North China.

    Science.gov (United States)

    Han, Bin; Liu, Yating; You, Yan; Xu, Jia; Zhou, Jian; Zhang, Jiefeng; Niu, Can; Zhang, Nan; He, Fei; Ding, Xiao; Bai, Zhipeng

    2016-10-01

    Assessment of the health risks resulting from exposure to ambient polycyclic aromatic hydrocarbons (PAHs) is limited by the lack of environmental exposure data among different subpopulations. To assess the exposure cancer risk of particulate carcinogenic polycyclic aromatic hydrocarbon pollution for the elderly, this study conducted a personal exposure measurement campaign for particulate PAHs in a community of Tianjin, a city in northern China. Personal exposure samples were collected from the elderly in non-heating (August-September, 2009) and heating periods (November-December, 2009), and 12 PAHs individuals were analyzed for risk estimation. Questionnaire and time-activity log were also recorded for each person. The probabilistic risk assessment model was integrated with Toxic Equivalent Factors (TEFs). Considering that the estimation of the applied dose for a given air pollutant is dependent on the inhalation rate, the inhalation rate from both EPA exposure factor book was applied to calculate the carcinogenic risk in this study. Monte Carlo simulation was used as a probabilistic risk assessment model, and risk simulation results indicated that the inhalation-ILCR values for both male and female subjects followed a lognormal distribution with a mean of 4.81 × 10-6 and 4.57 × 10-6, respectively. Furthermore, the 95 % probability lung cancer risks were greater than the USEPA acceptable level of 10-6 for both men and women through the inhalation route, revealing that exposure to PAHs posed an unacceptable potential cancer risk for the elderly in this study. As a result, some measures should be taken to reduce PAHs pollution and the exposure level to decrease the cancer risk for the general population, especially for the elderly.

  2. Our contaminated atmosphere: The danger of climate change, phases 1 and 2. [effect of atmospheric particulate matter on surface temperature and earth's radiation budget

    Science.gov (United States)

    Cimorelli, A. J.; House, F. B.

    1974-01-01

    The effects of increased concentrations of atmospheric particulate matter on average surface temperature and on the components of the earth's radiation budget are studied. An atmospheric model which couples particulate loading to surface temperature and to changes in the earth's radiation budget was used. A determination of the feasibility of using satellites to monitor the effect of increased atmospheric particulate concentrations is performed. It was found that: (1) a change in man-made particulate loading of a factor of 4 is sufficient to initiate an ice age; (2) variations in the global and hemispheric weighted averages of surface temperature, reflected radiant fluz and emitted radiant flux are nonlinear functions of particulate loading; and (3) a black satellite sphere meets the requirement of night time measurement sensitivity, but not the required day time sensitivity. A nonblack, spherical radiometer whose external optical properties are sensitive to either the reflected radiant fluz or the emitted radiant flux meets the observational sensitivity requirements.

  3. 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.

  4. 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.

  5. Genotoxicity of Polycyclic Aromatic Hydrocarbons and Nitro-Derived in Respirable Airborne Particulate Matter Collected from Urban Areas of Rio de Janeiro (Brazil)

    Science.gov (United States)

    Ramos de Rainho, Claudia; Machado Corrêa, Sérgio; Luiz Mazzei, José; Alessandra Fortes Aiub, Claudia

    2013-01-01

    Air pollution toxic effects are mainly attributed to small inhalable particulates with an aerodynamic diameter of less than 2.5 µm (PM 2.5). Our objective was to investigate mutagenic and clastogenic activity in PM samples collected in Rio de Janeiro. Samples were collected using a high-volume sampler at three sites: with low traffic and (2) and (3) with a heavy traffic. Six polycyclic aromatic hydrocarbons (PAHs) were quantified by gas chromatography/mass spectrometry (GC/MS). Salmonella typhimurium TA98 and the derivative strains YG1021 and YG1024 were used in mutagenicity assays in the presence of organic extracts (10–50 µg/ plate) with and without exogenous metabolization. Allium cepa test was performed to evaluate possible cytotoxic and clastogenic activities. The highest PM 2.5 µm (132.73 µm/m3) and PAH values (1.22 ng/m3 for benzo(a)pyrene) were detected at site 3. High mutagenic frameshift responses in absence and presence of metabolic activation were detected at site 3. The participation of nitroarenes and dinitroarenes was detected in the total mutagenicity of the extracts studied. The cytotoxic effect and the abnormalities detected by Allium cepa test can be attributed to the PAH nitroderivatives in the organic extracts. Evaluation of the genotoxicity of urban airborne particulate matter is important as a basis for decision making by regulatory authorities. PMID:23738331

  6. 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.

  7. 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 urban site during summer was mainly attributed to anthropogenic sources, with significant contribution from resuspension processes and long-range transport. The highest values of PHg0.7 and PHg2.2 were found during westerly and southerly wind events, reflecting local emission from highly polluted areas. The period from late fall to spring showed that advection from the southern part of Poland was the main factor responsible for elevated Hg concentrations in fine and coarse particles in the investigated region. Moreover, September 2013 could be given as an example of the influence of additional urban activities which occurred approx. 10 m from the sampling site-construction works connected with replacement of the road surface, asphalting, etc. The concentrations of particulate Hg (>600.0 pg m(-3)) were much higher than during the following months when any similar situation did not occur. Our investigations confirmed that Hg in urban aerosol samples was predominantly related to local industrial and commercial emissions, whereas the main source of Hg in particulate matter collected at the forest site was connected with regional anthropogenic processes. This paper provides the results of the first long-term measurements of size-fractionated particulate mercury conducted in central Poland, which could be an important insight into atmospheric Hg processes within such a scarcely investigated part of Europe.

  8. Desorption of Herbicides from Atmospheric Particulates During High-Volume Air Sampling

    Directory of Open Access Journals (Sweden)

    Dwight V. Quiring

    2011-11-01

    Full Text Available Pesticides can be present in the atmosphere either as vapours and/or in association with suspended particles. High-volume air sampling, in which air is aspirated first through a glass fibre filter to capture pesticides associated with atmospheric particulates and then polyurethane foam (PUF, often in combination with an adsorbent resin such as XAD-2, to capture pesticides present as vapours, is generally employed during atmospheric monitoring for pesticides. However, the particulate fraction may be underestimated because some pesticides may be stripped or desorbed from captured particulates due to the pressure drop created by the high flow of air through the filter. This possibility was investigated with ten herbicide active ingredients commonly used on the Canadian prairies (dimethylamine salts of 2,4-D, MCPA and dicamba, 2,4-D 2-ethylhexyl ester, bromoxynil octanoate, diclofop methyl ester, fenoxaprop ethyl ester, trifluralin, triallate and ethalfluralin and seven hydrolysis products (2,4-D, MCPA, dicamba, bromoxynil, diclofop, clopyralid and mecoprop. Finely ground heavy clay soil fortified with active ingredients/hydrolysis products was evenly distributed on the glass fibre filters of high-volume air samplers and air aspirated through the samplers at a flow rate of 12.5 m3/h for a 7-day period. The proportion desorbed as vapour from the fortified soil was determined by analysis of the PUF/XAD-2 resin composite cartridges. The extent of desorption from the fortified soil applied to the filters varied from 0% for each of the dimethylamine salts of 2,4-D, MCPA and dicamba to approximately 50% for trifluralin, triallate and ethalfluralin.

  9. 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.

  10. Characterization of atmospheric polycyclic aromatic hydrocarbons in a mixed-use urban community in Paterson, NJ: concentrations and sources.

    Science.gov (United States)

    Lin, Lin; Fan, Zhi-Hua; Zhu, Xianlei; Huang, Li-Hui; Bonanno, Linda J

    2011-06-01

    Exposure to ambient polycyclic aromatic hydrocarbons (PAHs) is a potential health concern for communities because many PAHs are known to be mutagenic and carcinogenic. However, information on ambient concentrations of PAHs in communities is very limited. During the Urban Community Air Toxics Monitoring Project, Paterson City, NJ, PAH concentrations in ambient air PM10 (particulate matter 202) to the total PAHs were significantly higher at the industrial site than those at the commercial and mobile sites. Analysis of the diagnostic ratios between PAH isomers suggested that the diesel-powered vehicles were the major PAH sources in the Paterson area throughout the year. The operation of industrial facilities and other combustion sources also partially contributed to PAH air pollution in Paterson. The correlation of individual PAH, total PAH, and the correlation of total PAHs with other air co-pollutants (copper, iron, manganese, lead, zinc, elemental carbon, and organic carbon) within and between the sampling sites supported the conclusions obtained from the diagnostic ratio analysis.

  11. 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. Copyright © 2016 Elsevier Ltd. All rights reserved.

  12. Distribution and Source of Polycyclic Aromatic Hydrocarbons (PAHs in Water Dissolved Phase, Suspended Particulate Matter and Sediment from Weihe River in Northwest China

    Directory of Open Access Journals (Sweden)

    Yuyun Chen

    2015-11-01

    Full Text Available Weihe River is a typical river located in the arid and semi-arid regions of Northwest China. In this study, the distribution and sources of 16 polycyclic aromatic hydrocarbons (PAHs in Weihe River were investigated. The concentrations of ∑PAHs ranged from 351 to 4427 ng/L with a mean value of 835.4 ng/L in water dissolved phase (WDP, from 3557 ng/L to 147,907 ng/L with a mean value of 20,780 ng /L in suspended particulate matter (SPM, and from 362 to 15,667 ng/g dry weight (dw with a mean value of 2000 ng/g dw in sediment, respectively. The concentrations of PAHs in Weihe River were higher compared with other rivers in the world. In both WDP and sediment, the highest concentrations of ∑PAHs were observed in the middle reach, while the lowest concentrations of ∑PAHs were found in the lower reach. For SPM, however, the PAHs concentrations in the lower reach were highest and the PAHs concentrations in the upper reach were lowest. The ratios of anthracene/(anthracene + phenanthrene and fluoranthene/ (fluoranthene + pyrene reflected a pattern of both pyrolytic and petrogenic input of PAHs in Weihe River. The potential ecosystem risk assessment indicated that harmful biological impairments occur frequently in Weihe River.

  13. N-alkanes and polycyclic aromatic hydrocarbons in total suspended particulates from the southeastern Tibetan Plateau: concentrations, seasonal variations, and sources.

    Science.gov (United States)

    Chen, Yang; Cao, Junji; Zhao, Jing; Xu, Hongmei; Arimoto, Richard; Wang, Gehui; Han, Yongming; Shen, Zhenxing; Li, Guohui

    2014-02-01

    Sixty-two suspended particle (TSP) samples were collected from Lulang on the southeastern Tibetan Plateau from July 2008 and July 2009 to investigate the concentrations, seasonal variations, and sources of n-alkanes and polycyclic aromatic hydrocarbons (PAHs). Samples were analyzed using thermal-deposition gas chromatography mass spectrometry. The concentrations of particulate total n-alkanes ranged from 0.10 to 21.83 ng m(-3), with an annual mean of 1.25 ng m(-3); the PAHs ranged from 0.06 to 2.53, with a mean of 0.59 ng m(-3). Up to 70% of PAHs were 5- and 6-ring compounds. The n-alkanes and PAHs both showed higher concentrations in winter and lower concentrations in summer. Analyses of diagnostic ratios indicate that 6.4% to 58.9% (mean 24.9%) of the n-alkanes were from plant waxes. Source characterization studies, i.e. diagnostic ratio and positive factor matrix analysis, suggest that the PAHs were from biomass burning as well as from fossil fuel combustion. Backward trajectory analysis suggests that the biomass mass burning pollutants could be from South Asia and western China via long distance transport. The study contributes to a more comprehensive understanding of the concentrations, seasonal variations, and sources of n-alkanes and PAHs in a remote background area in Tibetan Plateau. © 2013. Published by Elsevier B.V. All rights reserved.

  14. 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. Copyright © 2016 Elsevier Ltd. All rights reserved.

  15. Semiautomatic sequential extraction of polycyclic aromatic hydrocarbons and elemental bio-accessible fraction by accelerated solvent extraction on a single particulate matter sample.

    Science.gov (United States)

    Astolfi, Maria Luisa; Di Filippo, Patrizia; Gentili, Alessandra; Canepari, Silvia

    2017-11-01

    We describe the optimization and validation of a sequential extractive method for the determination of the polycyclic aromatic hydrocarbons (PAHs) and elements (Al, As, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Se, V and Zn) that are chemically fractionated into bio-accessible and mineralized residual fractions on a single particulate matter filter. The extraction is performed by automatic accelerated solvent extraction (ASE); samples are sequentially treated with dichloromethane/acetone (4:1) for PAHs extraction and acetate buffer (0.01M; pH 4.5) for elements extraction (bio-accessible fraction). The remaining solid sample is then collected and subjected to acid digestion with HNO3:H2O2 (2:1) to determine the mineralized residual element fraction. We also describe a homemade ASE cell that reduces the blank values for most elements; in this cell, the steel frit was replaced by a Teflon pierced disk and a Teflon cylinder was used as the filler. The performance of the proposed method was evaluated in terms of recovery from standard reference material (SRM 1648 and SRM 1649a) and repeatability. The equivalence between the new ASE method and conventional methods was verified for PAHs and for bio-accessible and mineralized residual fractions of elements on PM10 twin filters. Copyright © 2017 Elsevier B.V. All rights reserved.

  16. Characterizations, relationship, and potential sources of outdoor and indoor particulate matter bound polycyclic aromatic hydrocarbons (PAHs) in a community of Tianjin, Northern China.

    Science.gov (United States)

    Han, B; Bai, Z; Liu, Y; You, Y; Xu, J; Zhou, J; Zhang, J; Niu, C; Zhang, N; He, F; Ding, X

    2015-06-01

    Polycyclic aromatic hydrocarbons (PAHs) are among the most toxic air pollutants in China. However, because there are unsubstantial data on indoor and outdoor particulate PAHs, efforts in assessing inhalation exposure and cancer risk to PAHs are limited in China. This study measured 12 individual PAHs in indoor and outdoor environments at 36 homes during the non-heating period and heating period in 2009. Indoor PAH concentrations were comparable with outdoor environments in the non-heating period, but were lower in the heating period. The average indoor/outdoor ratios in both sampling periods were lower than 1, while the ratios in the non-heating period were higher than those in the heating period. Correlation analysis and coefficient of divergence also verified the difference between indoor and outdoor PAHs, which could be caused by high ventilation in the non-heating period. To support this conclusion, linear and robust regressions were used to estimate the infiltration factor to compare outdoor PAHs to indoor PAHs. The calculated infiltration factors obtained by the two models were similar in the non-heating period but varied greatly in the heating period, which may have been caused by the influence of ventilation. Potential sources were distinguished using a diagnostic ratio and a mixture of coal combustion and traffic emission, which are major sources of PAHs. © 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

  17. Distribution and Source of Polycyclic Aromatic Hydrocarbons (PAHs) in Water Dissolved Phase, Suspended Particulate Matter and Sediment from Weihe River in Northwest China.

    Science.gov (United States)

    Chen, Yuyun; Jia, Rui; Yang, Shengke

    2015-11-06

    Weihe River is a typical river located in the arid and semi-arid regions of Northwest China. In this study, the distribution and sources of 16 polycyclic aromatic hydrocarbons (PAHs) in Weihe River were investigated. The concentrations of ∑PAHs ranged from 351 to 4427 ng/L with a mean value of 835.4 ng/L in water dissolved phase (WDP), from 3557 ng/L to 147,907 ng/L with a mean value of 20,780 ng /L in suspended particulate matter (SPM), and from 362 to 15,667 ng/g dry weight (dw) with a mean value of 2000 ng/g dw in sediment, respectively. The concentrations of PAHs in Weihe River were higher compared with other rivers in the world. In both WDP and sediment, the highest concentrations of ∑PAHs were observed in the middle reach, while the lowest concentrations of ∑PAHs were found in the lower reach. For SPM, however, the PAHs concentrations in the lower reach were highest and the PAHs concentrations in the upper reach were lowest. The ratios of anthracene/(anthracene + phenanthrene) and fluoranthene/ (fluoranthene + pyrene) reflected a pattern of both pyrolytic and petrogenic input of PAHs in Weihe River. The potential ecosystem risk assessment indicated that harmful biological impairments occur frequently in Weihe River.

  18. The persistence of pesticides in atmospheric particulate phase: An emerging air quality issue

    Science.gov (United States)

    Socorro, Joanna; Durand, Amandine; Temime-Roussel, Brice; Gligorovski, Sasho; Wortham, Henri; Quivet, Etienne

    2016-09-01

    The persistent organic pollutants (POPs) due to their physicochemical properties can be widely spread all over the globe; as such they represent a serious threat to both humans and wildlife. According to Stockholm convention out of 24 officially recognized POPs, 16 are pesticides. The atmospheric life times of pesticides, up to now were estimated based on their gas-phase reactivity. It has been only speculated that sorption to aerosol particles may increase significantly the half-lives of pesticides in the atmosphere. The results presented here challenge the current view of the half-lives of pesticides in the lower boundary layer of the atmosphere and their impact on air quality and human health. We demonstrate that semivolatile pesticides which are mostly adsorbed on atmospheric aerosol particles are very persistent with respect to the highly reactive hydroxyl radicals (OH) that is the self-cleaning agent of the atmosphere. The half-lives in particulate phase of difenoconazole, tetraconazole, fipronil, oxadiazon, deltamethrin, cyprodinil, permethrin, and pendimethalin are in order of several days and even higher than one month, implying that these pesticides can be transported over long distances, reaching the remote regions all over the world; hence these pesticides shall be further evaluated prior to be confirmed as POPs.

  19. Characterisation of solvent extractable organic constituents in atmospheric particulate matter: an overview

    Directory of Open Access Journals (Sweden)

    Célia A. Alves

    2008-03-01

    Full Text Available In spite of accounting for 10-70% of the atmospheric aerosol mass, particulate-phase organic compounds are not well characterised, and many aspects of aerosol formation and evolution are still unknown. The growing awareness of the impact of particulate aerosols on climate, and the incompletely recognised but serious effects of anthropogenic constituents on air quality and human health, have conducted to several scientific studies. These investigations have provided information about the behaviour of atmospheric particulate matter and the description of the character of its carbonaceous content. The compilation of such results is important as they append to the emergent global-wide dataset of the organic composition of atmospheric aerosols. The contribution of the major emission sources to regional particulate pollution can be diagnosed by using specific molecular markers. This overview is mainly focused on results obtained with gas chromatography coupled with mass spectrometry, since it is the analytical method of choice in elucidating the solvent-extractable organic compounds in atmospheric particulate matter. A synopsis of the selection of organic tracers and the application of geochemical parameters to the analysis of organic constituents as a tool for source apportionment is shown here. Besides the assessment of current knowledge, this paper also presents the identification of further areas of concern.Apesar de constituirem 10-70% da massa do aerosol atmosférico, a caracterização dos compostos orgânicos particulados permanece ainda deficitária e vários aspectos relativos à formação e evolução do aerossol são ainda desconhecidos. A crescente preocupação com o impacto do aerosol particulado no clima e os reconhecidos efeitos dos constituintes antropogênicos na qualidade do ar e na saúde humana têm motivado a realização de numerosos estudos. Estas investigações têm fornecido informações relevantes sobre o comportamento

  20. Gas/particle partitioning of polycyclic aromatic hydrocarbons in coastal atmosphere of the north Yellow Sea, China.

    Science.gov (United States)

    Wang, Zhen; Ren, Peifang; Sun, Yan; Ma, Xindong; Liu, Xing; Na, Guangshui; Yao, Ziwei

    2013-08-01

    Samples of gas- and particle-phase polycyclic aromatic hydrocarbons (PAHs) were collected at three sampling stations (Xiaomai Island, Laohutan, and Zhangzi Island) in the north Yellow Sea, China during November 2008 and September 2009 to study their atmospheric transport potential and the gas/particle distributions. The composition of PAHs was dominated by gaseous compounds. The percentages of the particle-phase PAHs to the total concentrations were found to be higher during the heating period than the non-heating period. The ratios of naphthalene and acenaphthene to phenanthrene, chrysene and dibenzo(a,h)anthracene showed an increasing trend from Xiaomai Island to Zhangzi Island, which can be called as the local atmospheric distillation of PAHs. Gas/particle partitioning coefficients (K p) and their relationship with the sub-cooled liquid vapor pressures (pºL) of PAHs were investigated. The regressions of logK p versus logpºL gave significant correlations for all samples of the three sites with r (2) values in the range 0.56-0.66 (p<0.01). Both Junge-Pankow adsorption model and octanol-air partition coefficient absorption model tended to underestimate the sorption for most PAHs, but the absorption model appeared to be more suitable for predicting the particle fraction of PAHs than the Junge-Pankow model.

  1. 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.

  2. 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. Copyright © 2014 Elsevier Inc. All rights reserved.

  3. Development of a Novel Simulation Reactor for Chronic Exposure to Atmospheric Particulate Matter

    Science.gov (United States)

    Ye, Jianhuai; Salehi, Sepehr; North, Michelle L.; Portelli, Anjelica M.; Chow, Chung-Wai; Chan, Arthur W. H.

    2017-02-01

    Epidemiological studies have shown that air pollution is associated with the morbidity and mortality from cardiopulmonary diseases. Currently, limited experimental models are available to evaluate the physiological and cellular pathways activated by chronic multi-pollutant exposures. This manuscript describes an atmospheric simulation reactor (ASR) that was developed to investigate the health effects of air pollutants by permitting controlled chronic in vivo exposure of mice to combined particulate and gaseous pollutants. BALB/c mice were exposed for 1 hr/day for 3 consecutive days to secondary organic aerosol (SOA, a common particulate air pollutant) at 10-150 μg/m3, SOA (30 μg/m3) + ozone (65 ppb) or SOA + ozone (65 ppb) + nitrogen dioxide (NO2; 100 ppb). Daily exposure to SOA alone led to increased airway hyperresponsiveness (AHR) to methacholine with increasing SOA concentrations. Multi-pollutant exposure with ozone and/or NO2 in conjunction with a sub-toxic concentration of SOA resulted in additive effects on AHR to methacholine. Inflammatory cell recruitment to the airways was not observed in any of the exposure conditions. The ASR developed in this study allows us to evaluate the chronic health effects of relevant multi-pollutant exposures at ‘real-life’ levels under controlled conditions and permits repeated-exposure studies.

  4. Secondary ion mass spectrometry: The application in the analysis of atmospheric particulate matter

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Di; Hua, Xin; Xiu, Guang-Li; Zheng, Yong-Jie; Yu, Xiao-Ying; Long, Yi-Tao

    2017-10-01

    Currently, considerable attention has been paid to atmospheric particulate matter (PM) investigation due to its importance in human health and global climate change. Surface characterization of PM is important since the chemical heterogeneity between the surface and bulk may vary its impact on the environment and human being. Secondary ion mass spectrometry (SIMS) is a surface technique with high surface sensitivity, capable of high spatial chemical imaging and depth profiling. Recent research shows that SIMS holds great potential in analyzing both surface and bulk chemical information of PM. In this review, we presented the working principal of SIMS in PM characterization, summarized recent applications in PM analysis from different sources, discussed its advantages and limitations, and proposed the future development of this technique with a perspective in environmental sciences.

  5. Microphysical Characteristics of Atmospheric Particulate Matter from NASA’s MODIS, MISR, and AERONET Observations

    Science.gov (United States)

    Gad, N.; Shokr, M.; Ibrahim, Alaa

    2017-06-01

    We present a comparative study of atmospheric particulate matter (also known as aerosols) observed by satellite remote sensing and ground-based observations. We compare satellite measurements obtained by NASA’s Moderate Resolution Imaging Spectro-Radiometer (MODIS) and Multi-angle Imaging Spectro-Radiometer (MISR) instruments against the ground-based aerosol sun-photometer data from the Aerosol Robotic Network (AERONET) station in Cairo, Egypt from 2003 to 2014 to build a long-term database for climatological studies and to improve upon the accuracy and coverage achievable from the satellite data. We deduce microphysical and geometrical properties about the dominant aerosols based on key optical properties including aerosol optical depth (AOD), single scattering albedo (SSA), and Ångström exponent (AE). This has allowed us to place important constraints on the type of aerosols (natural, anthropogenic, and biogenic).

  6. Effects of Floor Level and Building Type on Residential Levels of Outdoor and Indoor Polycyclic Aromatic Hydrocarbons, Black Carbon, and Particulate Matter in New York City

    Directory of Open Access Journals (Sweden)

    Rachel L. Miller

    2011-05-01

    Full Text Available Consideration of the relationship between residential floor level and concentration of traffic-related airborne pollutants may predict individual residential exposure among inner city dwellers more accurately. Our objective was to characterize the vertical gradient of residential levels of polycyclic aromatic hydrocarbons (PAH; dichotomized into Σ8PAHsemivolatile (MW 178–206, and Σ8PAHnonvolatile (MW 228–278, black carbon (BC, PM2.5 (particulate matter by floor level (FL, season and building type. We hypothesize that PAH, BC and PM2.5 concentrations may decrease with higher FL and the vertical gradients of these compounds would be affected by heating season and building type. PAH, BC and PM2.5 were measured over a two-week period outdoor and indoor of the residences of a cohort of 5–6 year old children (n = 339 living in New York City’s Northern Manhattan and the Bronx. Airborne-pollutant levels were analyzed by three categorized FL groups (0–2nd, 3rd–5th, and 6th–32nd FL and two building types (low-rise versus high-rise apartment building. Indoor Σ8PAHnonvolatile and BC levels declined with increasing FL. During the nonheating season, the median outdoor Σ8PAHnonvolatile, but not Σ8PAHsemivolatile, level at 6th–2nd FL was 1.5–2 times lower than levels measured at lower FL. Similarly, outdoor and indoor BC concentrations at 6th–32nd FL were significantly lower than those at lower FL only during the nonheating season (p < 0.05. In addition, living in a low-rise building was associated significantly with higher levels of Σ8PAHnonvolatile and BC. These results suggest that young inner city children may be exposed to varying levels of air pollutants depending on their FL, season, and building type.

  7. Organic particulate material levels in the atmosphere: conditions favoring sensitivity to varying relative humidity and temperature.

    Science.gov (United States)

    Pankow, James F

    2010-04-13

    This study examines the sensitivity in predicted levels of atmospheric organic particulate matter (M(o), microg m(-3)) as those levels may potentially be affected by changes in relative humidity and temperature. In a given system, for each partitioning compound, f(g) and f(p) represent the gaseous and particulate fractions (f(g) + f(p) = 1). Sensitivity in the M(o) levels becomes dampened as the compounds contributing significantly to M(o) are increasingly found in the particle phase (f(p) --> 1). Thus, although local maxima in sensitivity can be encountered as M(o) levels increase, because as M(o) increases each f(p) --> 1, then increasing M(o) levels generally tend to reduce sensitivity in M(o) levels to changes in relative humidity and temperature. Experiments designed to elucidate the potential magnitudes of the effects of relative humidity and temperature on M(o) levels must be carried out at M(o) levels that are relevant for the ambient atmosphere: The f(p) values for the important partitioning compounds must not be elevated above ambient-relevant values. Systems in which M(o) levels are low (e.g., 1-2 microg m(-3)) and/or composed of unaged secondary organic aerosol are the ones most likely to show sensitivity to changing relative humidity and temperature. Results from two published chamber studies are examined in the above regard: [Warren B, et al. (2009) Atmos Environ 43:1789-1795] and [Prisle NL, et al. (2010) Geophys Res Lett 37:L01802].

  8. Polycyclic aromatic hydrocarbons - fate and long-range atmospheric transport studied using a global model, EMAC-SVOC

    Science.gov (United States)

    Octaviani, Mega; Tost, Holger; Lammel, Gerhard

    2017-04-01

    Polycyclic aromatic hydrocarbons (PAHs) are emitted by incomplete combustion from fossil fuel, vehicles, and biomass burning. They may persist in environmental compartments, pose a health hazard and may bio accumulate along food chains. The ECHAM/MESSy Atmospheric Chemistry (EMAC) model had been used to simulate global tropospheric, stratospheric chemistry and climate. In this study, we improve the model to include simulations of the transport and fate of semi-volatile organic compounds (SVOC). The EMAC-SVOC model takes into account essential environmental processes including gas-particle partitioning, dry and wet deposition, chemical and bio-degradation, and volatilization from sea surface, soils, vegetation, and snow. The model was evaluated against observational data in the Arctic, mid-latitudes, and tropics, and further applied to study total environmental lifetime and long-range transport potential (LRTP) of PAHs. We selected four compounds for study, spanning a wide range of volatility, i.e., phenanthrene, fluoranthene, pyrene, and benzo[a]pyrene. Several LRTP indicators were investigated, including the Arctic contamination potential, meridional spreading, and zonal and meridional fluxes to remote regions.

  9. Field measurements of the atmospheric dry deposition fluxes and velocities of polycyclic aromatic hydrocarbons to the global oceans.

    Science.gov (United States)

    González-Gaya, Belén; Zúñiga-Rival, Javier; Ojeda, María-José; Jiménez, Begoña; Dachs, Jordi

    2014-05-20

    The atmospheric dry deposition fluxes of 16 polycyclic aromatic hydrocarbons (PAHs) have been measured, for the first time, in the tropical and subtropical Atlantic, Pacific, and Indian Oceans. Depositional fluxes for fine (0.7-2.7 μm) and coarse (>2.7 μm) aerosol fractions were simultaneously determined with the suspended aerosol phase concentrations, allowing the determination of PAH deposition velocities (vD). PAH dry deposition fluxes (FDD) bound to coarse aerosols were higher than those of fine aerosols for 83% of the measurements. Average FDD for total (fine + coarse) Σ16PAHs (sum of 16 individual PAHs) ranged from 8.33 ng m(-2)d(-1) to 52.38 ng m(-2)d(-1). Mean FDD for coarse aerosol's individual PAHs ranged between 0.13 ng m(-2)d(-1) (Perylene) and 1.96 ng m(-2)d(-1) (Methyl Pyrene), and for the fine aerosol fraction these ranged between 0.06 ng m(-2)d(-1) (Dimethyl Pyrene) and 1.25 ng m(-2)d(-1) (Methyl Chrysene). The estimated deposition velocities went from the highest mean vD for Methyl Chrysene (0.17-13.30 cm s(-1)), followed by Dibenzo(ah)Anthracene (0.29-1.38 cm s(-1)), and other high MW PAHs to minimum values of vD for Dimethyl Pyrene (oceans.

  10. Development of 2-channel (532 nm and 355 nm) mobile LIDAR for mapping particulate matter in the atmosphere

    CSIR Research Space (South Africa)

    Sivakumar, V

    2010-09-01

    Full Text Available In this paper, the authors describe the developmentof 2-Channel (532 nm and 355 nm) mobile LIDAR system for studying atmospheric particulate matter. The system is currently tested in house at the Council for Scientific and Industrial Research...

  11. 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.

  12. The application of magnetic measurements for the characterization of atmospheric particulate pollution within the airport environment.

    Science.gov (United States)

    Jones, S; Richardson, N; Bennett, M; Hoon, S R

    2015-01-01

    The significant increase in global air travel which has occurred during the last fifty years has generated growing concern regarding the potential impacts associated with increasing emissions of atmospheric particulate matter (PM) on health and the environment. PM within the airport environment may be derived from a range of sources. To date, however, the identification of individual sources of airport derived PM has remained elusive but constitutes a research priority for the aviation industry.The aim of this research was to identify distinctive and characteristic fingerprints of atmospheric PM derived from various sources in an airport environment through the use of environmental magnetic measurements. PM samples from aircraft engine emissions, brake wear and tire wear residues have been obtained from a range of different aircraft and engine types. Samples have been analyzed utilizing a range of magnetic mineral properties indicative of magnetic mineralogy and grain size. Results indicate that the dusts from the three 'aircraft' sources, (i.e. engines, brakes and tires) display distinctive magnetic mineral characteristics which may serve as 'magnetic fingerprints' for these sources. Magnetic measurements of runway dusts collected at different locations on the runway surface also show contrasting magnetic characteristics which, when compared with those of the aircraft-derived samples, suggest that they may relate to different sources characteristic of aircraft emissions at various stages of the take-off/landing cycle. The findings suggest that magnetic measurements could have wider applicability for the differentiation and identification of PM within the airport environment.

  13. 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

  14. 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.

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

    Science.gov (United States)

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

    2017-05-01

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

  16. Azaarenes in fine particulate matter from the atmosphere of a Chinese megacity.

    Science.gov (United States)

    Bandowe, Benjamin A Musa; Meusel, Hannah; Huang, Rujin; Hoffmann, Thorsten; Cao, Junji; Ho, Kinfai

    2016-08-01

    Azaarenes (AZAs) are toxicologically relevant organic compounds with physicochemical properties that are significantly different from the well-studied polycyclic aromatic hydrocarbons (PAHs). However, little is known about their concentrations, seasonal variations, fate, and relationship with PAHs in air. This paper reports the temporal variations in the concentrations and composition patterns of AZAs in PM2.5 that was sampled once per 6 days from outdoor air of Xi'an, China from July 2008 to August 2009. The concentrations of the ∑AZAs, quinoline (QUI), benzo[h]quinoline (BQI), and acridine (ACR) in PM2.5 were 213-6441, 185-520, 69-2483, and 10-3544 pg m(-3), respectively. These concentrations were higher than those measured in urban areas of Western Europe. AZA compositional patterns were dominated by BQI and ACR. The high concentration of AZAs, high AZA/related PAH ratio, and the dominance of three-ring AZAs (BQI and ACR) in PM2.5 of Xi'an are all in contrast to observations from Western European and North American cities. This contrast likely reflects differences in coal type and the more intense use of coal in China. The PM2.5-bound concentration of AZA in winter season (W) was higher than during the summer season (S) with W/S ratios of 5.7, 1.4, 4.1, and 13, for ∑AZAs, QUI, BQI, and ACR, respectively. Despite their significantly different physicochemical properties, AZAs were significantly (p < 0.05) positively correlated with their related PAHs and pyrogenic elemental carbon. The changes in AZA concentrations were positively correlated with ambient pressure but negatively correlated with ambient temperature, wind speed, and relative humidity. This trend is similar to that observed for the related PAHs. We conclude that Xi'an and possibly other Chinese cities have higher emission of AZAs into their atmosphere because of the more pronounced use of coal. We also conclude that in spite of differences in physicochemical properties between AZAs and

  17. Diurnal variations of ambient particulate wood burning emissions and their contribution to the concentration of Polycyclic Aromatic Hydrocarbons (PAHs) in Seiffen, Germany

    Science.gov (United States)

    Poulain, L.; Iinuma, Y.; Müller, K.; Birmili, W.; Weinhold, K.; Brüggemann, E.; Gnauk, T.; Hausmann, A.; Löschau, G.; Wiedensohler, A.; Herrmann, H.

    2011-12-01

    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), and Oxygenated Organic Aerosol (OOA) were identified and represented 20%, 17% and 62% of total OA, respectively. Additionally, Polycyclic Aromatic Hydrocarbons (PAH) were measured by the AMS with an average concentration of 10 ng m-3 and short term events of extremely high PAH concentration (up to 500 ng m-3) 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 low correlation with CO and the low car traffic, the HOA factor was considered to be related to residential heating using liquid fuel. An influence of the time of the week (week vs. weekend) 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 only one maximum in the afternoon. Finally, the PAH emitted directly from residential wood combustion was estimated to represent 1.5% of the total mass of the BBOA factor and around 62% of the total PAH concentration measured at

  18. Diurnal variations of ambient particulate wood burning emissions and their contribution to the concentration of Polycyclic Aromatic Hydrocarbons (PAHs in Seiffen, Germany

    Directory of Open Access Journals (Sweden)

    L. Poulain

    2011-12-01

    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, and Oxygenated Organic Aerosol (OOA were identified and represented 20%, 17% and 62% of total OA, respectively. Additionally, Polycyclic Aromatic Hydrocarbons (PAH were measured by the AMS with an average concentration of 10 ng m−3 and short term events of extremely high PAH concentration (up to 500 ng m−3 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 low correlation with CO and the low car traffic, the HOA factor was considered to be related to residential heating using liquid fuel. An influence of the time of the week (week vs. weekend 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 only one maximum in the afternoon. Finally, the PAH emitted directly from residential wood combustion was estimated to represent 1.5% of the total mass of the BBOA factor and

  19. 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

  20. Research on chromium and arsenic speciation in atmospheric particulate matter: short review

    Science.gov (United States)

    Nocoń, Katarzyna; Rogula-Kozłowska, Wioletta; Widziewicz, Kamila

    2018-01-01

    Atmospheric particulate matter (PM) plays an important role in the distribution of elements in the environment. The PM-bound elements penetrates into the other elements of the environment, in two basic forms - those dissolved in the atmospheric precipitation and those permanently bound to PM particles. Those forms differs greatly in their mobility, thus posing a potential threat to living organisms. They can also be an immediate threat, while being inhaled. Chromium (Cr) and arsenic (As) belong to the group of elements whose certain chemical states exhibit toxic properties, that is Cr(VI) and As(III). Thus, recognition of the actual threat posed by Cr and As in the environment, including those present in PM, is possible only through the in depth speciation analysis. Research on the Cr and As speciation in PM, more than the analogous studies of their presence in other compartments of the environment, have been undertaken quite rarely. Hence the knowledge on the speciation of PM-bound As and Cr is still limited. The state of knowledge in the field of PM-bound Cr and As is presented in the paper. The issues related to the characterization and occurrence of Cr and As species in PM, the share of Cr and As species mass in different PM size fractions, and in PM of different origin is also summarized. The analytical techniques used in the speciation analysis of PM-bound Cr and As are also discussed. In the existing literature there is no data on the physical characteristics of Cr and As (bound to a different PM size fractions), and thus it still lack of data needed for a comprehensive assessment of the actual environmental and health threat posed by airborne Cr and As.

  1. Synoptic and climatological analysis of atmospheric circulation impacts on particulate matter pollution in Shanghai, China

    Science.gov (United States)

    Liao, Z.; Fan, S.

    2016-12-01

    This study investigated the particulate matter characteristics within different circulation types (CTs) in the megacity of Shanghai during the period 2001-2015, and provided a quantitative evaluation of atmospheric circulation influences on PM10 pollution across a wide range of spatial and temporal scales, from local to region and daily to interannual. Ten CTs were identified over the Asian-Pacific region by objective Lamb Weather Type approach and each resulting CT was characterized with distinct local meteorology and air mass source. The PM10 loadings in the CTs associated with continental westerly flow were significant higher than that in the CTs linked to marine easterly air masses. Regional backgrounds that transported by the synoptic flows were more responsible for the distinct PM10 levels in different CTs. The locally-produced PM10 generally stabilized in range of 20-25 μg m-3, but enhanced to 41.2 μg m-3 in case of anticyclone type. There were distinct PM10 trends in different CTs (ranged from -3.74 to -0.28 μg m-3 yr-1), indicating the different background trends. Overall, the PM10 concentrations have decreased (-2.33 μg m-3 yr-1) in the studied period and the estimated locally-produced trend (-0.79 μg m-3 yr-1) accounted for 33.9% of overall downward trend. The occurrence frequency presented an increase (0.15 % yr-1) for anticyclone type, but a decrease (-0.10 % yr-1) for the type N associated with invasion of cold air. The 15-yr frequency change of atmospheric circulation induced an increase in PM­10 level (0.17 μg m-3) in Shanghai. On the contrary, controls on the pollutant emission had always positive effects and hence should be always encouraged.

  2. 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.

  3. Particulate matter and heavy metals in the atmospheric aerosol from Cartagena, Spain

    Science.gov (United States)

    Moreno-Grau, S.; Pérez-Tornell, A.; Bayo, J.; Moreno, J.; Angosto, J. M.; Moreno-Clavel, J.

    Total suspended particulate matter (TSP) and lead (Pb) concentrations were monitored at three sampling stations in Cartagena, Spain, from February 1990 to December 1998, and copper (Cu), zinc (Zn), and cadmium (Cd) atmospheric concentrations were measured from January 1991 to December 1998. TSP and Pb values were analysed from samples collected on glassfibre filters, and the concentrations of Pb, Cu, Zn, and Cd were calculated from cellulose ester filters, showing no statistically significant difference (95% C.L.) for Pb analysed in both filter types. The geographical and temporal distribution patterns were investigated. There was a trend to find the highest TSP levels during winter and autumn, and the highest Pb concentrations during the winter season. The Pb/Cd average ratios for each sampling point showed a direct anthropogenic contribution for the industrial areas, when compared with Pb/Cd ratio reported for global natural emissions. The correlation among heavy metals displayed similar results, differing from the residential area to the urban and industrial ones.

  4. Simultaneous atmospheric correction and quantification of suspended particulate matter in the Guadalquivir estuary from Landsat images

    Science.gov (United States)

    Carpintero, M.; Polo, M. J.; Suhyp Salama, Mhd.

    2015-05-01

    Earth observations (EOs) following empirical and/or analytical approaches are a feasible alternative to obtain spatial and temporal distribution of water quality variables. The limitations observed in the use of empirical approaches to estimate high concentrations of suspended particulate matter (SPM) in the estuarine water of Guadalquivir have led the authors to use a semi-analytical model, which relates the water constituents' concentration to the water leaving reflectance. In this work, the atmospheric correction has been carried out simultaneously and the aerosol reflectance and backscattering coefficients of SPM obtained. The results are validated using in situ SPM data series provided by a monitoring network in the study area. The results show that the model allows us to successfully estimate backscattering coefficients of SPM in the estuary, differentiating clear and turbid water and using two ɛ(4,5) .These considerations improve the value of R2 from 0.68 (single ɛ(4,5)) to 0.86 (two ɛ( 4,5)) on 18 May 2009. This method could be used as a preliminary approach to obtain SPM concentration in the Guadalquivir estuary with the limitations that the model shows for turbid waters.

  5. Simultaneous atmospheric correction and quantification of suspended particulate matter in the Guadalquivir estuary from Landsat images

    Directory of Open Access Journals (Sweden)

    M. Carpintero

    2015-05-01

    Full Text Available Earth observations (EOs following empirical and/or analytical approaches are a feasible alternative to obtain spatial and temporal distribution of water quality variables. The limitations observed in the use of empirical approaches to estimate high concentrations of suspended particulate matter (SPM in the estuarine water of Guadalquivir have led the authors to use a semi-analytical model, which relates the water constituents’ concentration to the water leaving reflectance. In this work, the atmospheric correction has been carried out simultaneously and the aerosol reflectance and backscattering coefficients of SPM obtained. The results are validated using in situ SPM data series provided by a monitoring network in the study area. The results show that the model allows us to successfully estimate backscattering coefficients of SPM in the estuary, differentiating clear and turbid water and using two ε(4,5 .These considerations improve the value of R2 from 0.68 (single ε(4,5 to 0.86 (two ε( 4,5 on 18 May 2009. This method could be used as a preliminary approach to obtain SPM concentration in the Guadalquivir estuary with the limitations that the model shows for turbid waters.

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

    DEFF Research Database (Denmark)

    Feilberg, Anders; Nielsen, Torben; Binderup, Mona-Lise

    2002-01-01

    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 po...

  7. The Development of a Mechanism to Model the Formation and Decay of Nitrated Polycyclic Aromatic Hydrocarbons in the Atmosphere.

    Science.gov (United States)

    Fan, Zhihua

    1995-01-01

    The overall purpose of this work is to develop a mechanism to model the formation and degradation of nitrated polycyclic aromatic hydrocarbons (NPAH) in the atmosphere. This work developed the processes relevant to the formation and degradation of NPAH, specially for fluoranthene (FL), pyrene (PY), and their derivatives, such as 1-nitropyrene (1NP), 2-nitrofluoranthene (2NF). Photostability of particle associated NPAH was investigated under sunlight on diesel exhaust or wood smoke particles in our 190 m^3 outdoor smog chamber in cold and warm temperatures. Rapid degradation of deuterated and native NPAH was observed in sunlight, even in cold temperatures (temperatures ranged between rm-18.6^circ C and -5.6^circ C). The photolysis rate of NPAH was referenced to the NO_2 photolysis rate in order to relate the observed decay of NPAH to the changing solar radiation. Based on the known chemistry of PAH and NPAH, a reaction mechanism for PAH and NPAH in the gas and particle phase in the atmosphere was proposed. The mechanism was evaluated with outdoor smog chamber experiments with diluted diesel exhaust under different initial photochemical conditions. Simulations for FL and PY in both gas and particle phase were close to chamber observations. Formation of 2NF was observed in the chamber, but 2NP degraded rapidly under photochemical conditions. Mono- nitro-pyrenes (NPs) and nitro-fluoranthenes (NFs) were almost exclusively found in particle associated extracts. This implied that no or non-detectable 2NF or 2NP were distributed in the gas phase and that they were deposited on particles immediately after formation in the gas phase by the photochemical processes. To model the decay of NPAH on diesel particles, a rate Of k _{rm NPAH} = (0.04+/-0.01)times k_{NO2} was used for the decay of NPs, and a rate of rm k_{NPAH } = (0.025+/-0.005)times k_{NO2 } was needed to model the behavior of NFs. A higher rate, rm k_{NPAH} = (0.050+/-0.005)times k_{NO2} was needed to model NFs and

  8. 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.

  9. [Particulate matter and atmospheric pollutants exposure for outdoor workers in the Muggia area (Trieste, Italy)].

    Science.gov (United States)

    Urbani, Ranieri; Barbieri, Pierluigi; Cozzutto, Sergio; Barbieri, Gianpiero; Sist, Paola

    2011-01-01

    Urban air pollution originates from traffic, heating and industrial activities and it exposes several categories of workers to noxious chemicals; in recent years various surveys have been carried on taxi drivers, bus drivers, policemen, newspaper kiosks, fuel station workers and general population, for assessing exposure to main contaminants, benzene and PAHs in particular. defining a specific sampling strategy for collecting an experimental data base for the assessment of potential population exposure to atmospheric particulate matter in the Muggia area (Trieste, North-East Italy). A sample of 14 urban police officers working mainly on the roads and potentially subject to occupational exposure has been analyzed, as well as a sample of the municipal administrative personnel (13 people) working in indoor environments during the same sampling periods. Exposure has been monitored by personal samplers and high volume environmental samples; urinary levels of 1 OH-pyrene and creatinine were collected for each participant at the end of each sampling period. PAHs analyses provided diagnostic ratios for identification of the sources of pollution. In general experimental BaP values stay below the environmental target value, with satisfactory agreement between environmental and personal monitoring. Levels of urinary 1 OH-pyrene for administrative personnel was detected always below the background value (0.089 micromoles/mole creatinine), while they are above the background and below the attention value for most of urban police officers. Municipal police officers participating to the present study, while belonging to one of the categories of people most exposed to outdoor PM, do not show any worrying exposure to the considered chemicals associated to their occupational activity, in comparison to other factors, possibly associated to personal lifestyles.

  10. Polycyclic aromatic hydrocarbons in urban atmosphere of Guangzhou, China: Size distribution characteristics and size-resolved gas-particle partitioning

    Science.gov (United States)

    Yu, Huan; Yu, Jian Zhen

    2012-07-01

    Size distributions of thirteen polycyclic aromatic hydrocarbons (PAHs), elemental carbon (EC), and organic carbon (OC) in the range of 0.01-18 μm were measured using a nano Micro-Orifice Uniform Deposit Impactor (nano-MOUDI) in an urban location in Guangzhou, China in July 2006. PAH size distributions were fit with five modes and the respective mass median aerodynamic diameters (MMAD) are: Aitken mode (MMAD: ˜0.05 μm), three accumulation modes AMI, AMII, AMIII (MMAD: 0.13-0.17 μm, 0.4-0.45 μm, and 0.9-1.2 μm, respectively), and coarse mode (MMAD: 4-6 μm). Seven-ring PAH was mainly in AMII and AMIII. Five- and six-ring PAHs were found to be abundant in all the three AM. Three- and four-ring PAHs had a significant presence in the coarse mode in addition to the three AM. Size-resolved gas-particle partition coefficients of PAHs (Kp) were estimated using measured EC and OC data. The Kp values of a given PAH could differ by a factor of up to ˜7 on particles in different size modes, with the highest Kp associated with the AMI particles and the lowest Kp associated with the coarse mode particles. Comparison of calculated overall Kp with measured Kp values in Guangzhou by Yang et al. (2010) shows that adsorption on EC appeared to be the dominant mechanism driving the gas-particle partitioning of three- and four-ring PAHs while absorption in OM played a dominant role for five- and six-ring PAHs. The calculated equilibrium timescales of repartitioning indicate that five- to seven-ring PAHs could not achieve equilibrium partitioning within their typical residence time in urban atmospheres, while three- and four-ring PAHs could readily reach new equilibrium states in particles of all sizes. A partitioning flux is therefore proposed to replace the equilibrium assumption in modeling PAH transport and fate.

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

    Science.gov (United States)

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

    2008-01-01

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

  12. Characterization of atmospheric trace gases and particulate matter in Hangzhou, China

    Directory of Open Access Journals (Sweden)

    G. Zhang

    2018-02-01

    Full Text Available The Yangtze River Delta (YRD is one of the most densely populated regions in China with severe air quality issues that have not been fully understood. Thus, in this study, based on 1-year (2013 continuous measurement at a National Reference Climatological Station (NRCS, 30.22° N, 120.17° E; 41.7 m a.s.l. in the center of Hangzhou in the YRD, we investigated the seasonal characteristics, interspecies relationships, and the local emissions and the regional potential source contributions of trace gases (including O3, NOx, NOy, SO2, and CO and particulate matter (PM2.5 and PM10. Results revealed that severe two-tier air pollution (photochemical and haze pollution occurred in this region, with frequent exceedances in O3 (38 days and PM2.5 (62 days. O3 and PM2.5 both exhibited distinct seasonal variations with reversed patterns: O3 reaching a maximum in warm seasons (May and July but PM2.5 reaching a maximum in cold seasons (November to January. The overall results from interspecies correlation indicated a strong local photochemistry favoring the O3 production under a volatile organic compound (VOC-limited regime, whereas it moved towards an optimum O3 production zone during warm seasons, accompanied by the formation of secondary fine particulates under high O3. The emission maps of PM2.5, CO, NOx, and SO2 demonstrated that local emissions were significant for these species on a seasonal scale. The contributions from the regional transport among inland cities (Zhejiang, Jiangsu, Anhui, and Jiangxi Province on a seasonal scale were further confirmed to be crucial to air pollution at the NRCS site by using backward trajectory simulations. Air masses transported from the offshore areas of the Yellow Sea, East Sea, and South Sea were also found to be highly relevant to the elevated O3 at the NRCS site through the analysis of potential source contribution function (PSCF. Case studies of photochemical pollution (O3 and haze (PM2.5 episodes both

  13. An index for estimating the potential metal pollution contribution to atmospheric particulate matter from road dust in Beijing.

    Science.gov (United States)

    Zhao, Hongtao; Shao, Yaping; Yin, Chengqing; Jiang, Yan; Li, Xuyong

    2016-04-15

    The resuspension of road dust from street surfaces could be a big contributor to atmospheric particulate pollution in the rapid urbanization context in the world. However, to date what its potential contribution to the spatial pattern is little known. Here we developed an innovative index model called the road dust index (RIBeijing region to assess the spatial distribution of the potential risks posed by metals associated with road dust on atmospheric suspended particles. The results demonstrated that the road dust in urban areas has higher potential risk of metal to atmospheric particles than that in rural areas. The RIpollution caused by road dust emissions. Copyright © 2016 Elsevier B.V. All rights reserved.

  14. Measurement of polycyclic aromatic hydrocarbons and other pollutants.

    Science.gov (United States)

    Espigares García, M; Pérez López, J A; Mariscal Larrubia, A; Fernandez-Crehuet, M; Gálvez Vargas, R

    1987-04-01

    A single point study of atmospheric pollution has been carried out in Granada (Spain); suspended particulate matter, sulphur oxides, ammoniac, nitrogen dioxide and polycyclic aromatic hydrocarbons were determined. There were variations in relation to the month and the day of the week. The PAHs have been determined through HPLC, with a mobile phase of acetonitrile-water (75-25). The results of measurements of benzo(a)pyrene were between 1.006 and 0.485 micrograms m-3 in two different periods of sampling.

  15. [Exploration of a quantitative methodology to characterize the retention of PM2.5 and other atmospheric particulate matter by plant leaves: taking Populus tomentosa as an example].

    Science.gov (United States)

    Zhang, Zhi-Dan; Xi, Ben-Ye; Cao, Zhi-Guo; Jia, Li-Ming

    2014-08-01

    Taking Populus tomentosa as an example, a methodology called elution-weighing-particle size-analysis (EWPA) was proposed to evaluate quantitatively the ability of retaining fine particulate matter (PM2.5, diameter d ≤ 2.5 μm) and atmospheric particulate matter by plant leaves using laser particle size analyzer and balance. This method achieved a direct, accurate measurement with superior operability about the quality and particle size distribution of atmospheric particulate matter retained by plant leaves. First, a pre-experiment was taken to test the stability of the method. After cleaning, centrifugation and drying, the particulate matter was collected and weighed, and then its particle size distribution was analyzed by laser particle size analyzer. Finally, the mass of particulate matter retained by unit area of leaf and stand was translated from the leaf area and leaf area index. This method was applied to a P. tomentosa stand which had not experienced rain for 27 days in Beijing Olympic Forest Park. The results showed that the average particle size of the atmospheric particulate matter retained by P. tomentosa was 17.8 μm, and the volume percentages of the retained PM2.5, inhalable particulate matter (PM10, d ≤ 10 μm) and total suspended particle (TSP, d ≤ 100 μm) were 13.7%, 47.2%, and 99.9%, respectively. The masses of PM2.5, PM10, TSP and total particulate matter were 8.88 x 10(-6), 30.6 x 10(-6), 64.7 x 10(-6) and 64.8 x 10(-6) g x cm(-2) respectively. The retention quantities of PM2.5, PM10, TSP and total particulate matter by the P. tomentosa stand were 0.963, 3.32, 7.01 and 7.02 kg x hm(-2), respectively.

  16. Disposable sputtered-bismuth screen-printed sensors for voltammetric monitoring of cadmium and lead in atmospheric particulate matter samples.

    Science.gov (United States)

    Palomo-Marín, M R; Rueda-Holgado, F; Marín-Expósito, J; Pinilla-Gil, E

    2017-12-01

    We report here the use of commercial screen-printed disposable sensors comprising a sputtered bismuth working electrode, a silver pseudo reference electrode and a carbon auxiliary electrode (whole set referred as Bi sp SPE), as a new and advantageous alternative for reliable and convenient monitoring of Cd and Pb in atmospheric particulate matter (PM10 fraction) by anodic stripping voltammetry after acid digestion. After a detailed exploration of surface composition and depth profiles of the Bi sp SPE by SEM, EDX, XPS and EIS, chemical and instrumental variables have been optimized to develop a reliable method capable of measuring Cd and Pb with detection limits of 11.8ngmL -1 and 6.1ngmL -1 respectively. These detection limits are useful for pollution monitoring of these elements in ambient air under the requirements of international health and environmental protection standards. The accuracy of the method was assessed by voltammetric measurements of Cd and Pb in ERM®-CZ120 Fine dust (PM10-like) and ERM® 1648a Urban Particulate Matter certified reference materials. The applicability of the method to Cd and Pb determination in real samples was demonstrated by analysis of PM10 samples from the air quality network in Extremadura, with a good correlation respect to the standard ICP-MS methodology. Our work constitutes the first reference about the use of disposable sensors based on Bi sp SPE for the determination of heavy metals in atmospheric particulate matter samples. Copyright © 2017 Elsevier B.V. All rights reserved.

  17. Temporal Variation of Atmospheric Aerosol Particulate Matters and Heavy Metal Concentrations in Dhaka, Bangladesh

    Directory of Open Access Journals (Sweden)

    Tanzir Al Mahmud, , and *

    2008-06-01

    Full Text Available Aerosol particulate matters and heavy metal concentrations were measured for the period of August and September 2005 in Dhaka a Southeast Asian Mega City. Particulate matters (PM of different size fractions (TSP, PM10 and PM2.5 were collected on the micro fiber filters by placing the PM sampler on the roof of the Mohkarram Hossain Khundhkar Biggan Bhaban at the Department of Chemistry, University of Dhaka, Bangladesh. The overall average concentrations of TSP, PM10 and PM2.5 were 68, 43 and 35 µg m-3, respectively. About 82% particles were from fine fraction (PM2.5 and 18% were from coarse fraction (PM10-2.5, which indicates mechanical processes are one of the main sources for the particulate matters in Dhaka. Heavy metals (lead, copper, zinc, and iron concentrations were determined by using atomic absorption spectrophotometer (AAS for the size fraction of PM10 with highest concentrations recorded for iron (2360 ng m-3 and lowest for copper (28 ng m-3. The average concentration for lead (96 ng m-3 was lower than the WHO guideline value and also lower than the previous measurements in Dhaka. The lower concentration of lead was found presumably due to the official ban of leaded gasoline in Dhaka, Bangladesh.

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

    Directory of Open Access Journals (Sweden)

    X. K. Wang

    2016-02-01

    Full Text Available 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.

  19. Atmospheric Correction of Satellite GF-1/WFV Imagery and Quantitative Estimation of Suspended Particulate Matter in the Yangtze Estuary

    Directory of Open Access Journals (Sweden)

    Pei Shang

    2016-11-01

    Full Text Available The Multispectral Wide Field of View (WFV camera on the Chinese GF-1 satellite, launched in 2013, has advantages of high spatial resolution (16 m, short revisit period (4 days and wide scene swath (800 km compared to the Landsat-8/OLI, which make it an ideal means of monitoring spatial-temporal changes of Suspended Particulate Matter (SPM in large estuaries like the Yangtze Estuary. However, a lack of proper atmospheric correction methods has limited its application in water quality assessment. We propose an atmospheric correction method based on a look up table coupled by the atmosphere radiative transfer model (6S and the water semi-empirical radiative transfer (SERT model for inversion of water-leaving reflectance from GF-1 top-of-atmosphere radiance, and then retrieving SPM concentration from water-leaving radiance reflectance of the Yangtze Estuary and its adjacent sea. Results are validated by the Landsat-8/OLI imagery together with autonomous fixed station data, and influences of human activities (e.g., waterway construction and shipping on SPM distribution are analyzed.

  20. Seasonal variations and sources of atmospheric polycyclic aromatic hydrocarbons and organochlorine compounds in a high-altitude city: Evidence from four-year observations

    Energy Technology Data Exchange (ETDEWEB)

    Gong, Ping; Wang, Xiaoping; Sheng, Jiujiang; Wang, Hailong; Yuan, Xiaohua; He, Yuanqing; Qian, Yun; Yao, Tandong

    2018-02-01

    Lijiang is a high-altitude city located on the eastern fringe of the Tibetan Plateau, with complex seasonal atmospheric circulations (i.e. westerly wind, Indian Monsoon, and East Asia Monsoon). Very few previous studies have focused on seasonal variations and sources of organic pollutants in Lijiang. In this study, a four-year air campaign from June 2009 to July 2013 was conducted to investigate the temporal trends and the sources of polycyclic aromatic hydrocarbons (PAHs) and organochlorine compounds [including organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs)]. The atmospheric PAH concentrations in winter are 2-3 times of those in summer, probably because of the combined result of enhanced local emission and long-range atmospheric transport (LRAT) during winter. Traffic pollution was the primary local source of PAHs, while biomass burning is the dominant LRAT source. Different from PAHs, OCPs and PCBs mainly underwent LRAT to reach Lijiang. The peak concentrations of most of OCPs occurred in pre-monsoon season and winter, which are carried by air masses from Myanmar and India through westerly winds. As compared with other sites of the Tibetan Plateau, without the direct barrier of the Himalaya, Lijiang is easily contaminated by the incursion of polluted air masses.

  1. 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

  2. Determination of atmospheric gaseous and particulate sulfur compounds. [Atmospheric SO/sub 2/ sampling, calibration, and data processing

    Energy Technology Data Exchange (ETDEWEB)

    Tanner, R.L.; Forrest, J.; Newman, L.

    1977-01-01

    The corrosive influence of atmospheric sulfur compounds to man's health and his environment has been demonstratably costly. Damage to building materials, textiles, animals, plants, and artworks have been well documented and can in some cases be directly translated into financial loss. Indirect effects such as contribution to respiratory disease and increased death rates are more subtle but no less real. For both economic and ecological reasons, it has become imperative that atmospheric concentrations be minimized. Anthropogenic sources of atmospheric sulfur compounds are principally the combustion of fossil fuels, which produce sulfur dioxide along with several percent of sulfur trioxide. The predominant form of atmospheric gaseous sulfur is sulfur dioxide, accompanied by small amounts of hydrogen sulfide and organic sulfur compounds such as mercaptans and sulfides. Aerosol sulfur exists primarily as sulfates, including bisulfate and sulfuric acid. The core of any monitoring system is the analytical instrument or technique. Methods for SO/sub 2/ sampling, calibration, and data acquisition and reduction are reviewed. 305 references.

  3. 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

  4. Atmospheric dispersion modelling of particulate and gaseous pollutants affecting the trans-Manche region

    OpenAIRE

    Plainiotis, Stylianos

    2006-01-01

    This thesis describes the development of a methodology to determine large-scale and meso-scale atmospheric dispersion patterns. The research is only concerned with outdoor exposure to atmospheric pollutants and aims to identify pollution sources using dispersion modelling with the assistance of ground level measurements from British, French and other monitoring stations and remote sensing technology. \\ud \\ud Lagrangian Particle Dispersion (LPD) models compute trajectories of a large number of...

  5. Trans-Pacific and Regional Atmospheric Transport of Polycyclic Aromatic Hydrocarbons and Pesticides in Biomass Burning Emissions to Western North America

    Science.gov (United States)

    Genualdi, Susan A.; Killin, Robert K.; Woods, Jim; Wilson, Glenn; Schmedding, David; Massey Simonich, Staci L.

    2014-01-01

    The trans-Pacific and regional North American atmospheric transport of polycyclic aromatic hydrocarbons (PAHs) and pesticides in biomass burning emissions was measured in air masses from April to September 2003 at two remote sites in western North America. Mary’s Peak Observatory (MPO) is located in Oregon’s Coast Range and Cheeka Peak Observatory (CPO) is located on the tip of the Olympic Peninsula in Washington State. During this time period, both remote sites were influenced by PAH and pesticide emissions from forest fires in Siberia and regional fires in Oregon and Washington State. Concurrent samples were taken at both sites on June 2 and August 4, 2003. On these dates, CPO had elevated gas phase PAH, alpha-hexachlorocyclohexane and retene concentrations (ppesticide mass was lost from soil due to burning. These data suggest that the transPacific and regional atmospheric transport of biomass burning emissions results in elevated PAH and pesticide concentrations in western North America. The elevated pesticide concentrations are likely due to re-emission of historically deposited pesticides from the soil and vegetation during the fire event. PMID:19320158

  6. 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.

  7. Impact of abandoned mine waste on atmospheric respirable particulate matter in the historic mining district of Rio Tinto (Iberian Pyrite Belt).

    Science.gov (United States)

    Sánchez de la Campa, Ana M; de la Rosa, Jesús D; Fernández-Caliani, Juan C; González-Castanedo, Yolanda

    2011-11-01

    This work documents for the first time the levels and composition of atmospheric particulate matter in the historic mining district of Rio Tinto (Spain) to estimate the contribution and impact of resuspended particles from hazardous mine waste on air quality. The resuspended mine waste dust contributes notably (32%) to the total concentrations of toxic trace metals (Bi, As, Cu, Pb, Cd, Zn and Sb) into the atmosphere, with the consequent impact on public health. Copyright © 2011 Elsevier Inc. All rights reserved.

  8. Atmospheric Ammonia and Particulate Inorganic Nitrogen Monitoring in the United States - A Comparison Study

    Science.gov (United States)

    Kariyawasam, T.

    2016-12-01

    Due to emission by disproportionately high livestock numbers and increased nitrogen fertilization, Ammonia (NH3) has come to play an increasingly important role in the global biogeochemical cycle of reactive nitrogen as well as in secondary aerosol formation and climate. Because of the public health problems it causes and the effects on the atmosphere, monitoring the global distribution of NH3 sources becomes crucial. Accurate measurements of atmospheric NH3 via ground level sensors and satellites are fundamentally essential for meteorological forecasting, hazard warning and various other applications. Since the NH3 retrieval quality is affected by meteorological properties, such as the vertical temperature, water vapor profiles, surface temperatures, and emissivity, which are used to model the atmosphere, even though satellite systems has the capability of monitoring environmental variables with high temporal and spatial coverages, they lack precision at or near ground level. Due to cost of implementation and technical maintenance constraints, daily global coverage of accurate NH3 in situ measurements from ground based sensors is also often limited in spatial representation. In research related to climate and atmospheric physics, the advances in sensor technology have led to the use of automated sensors in a variety of climate and atmospheric data analysis applications. The extant research is expanding further but lacks a framework to consider the current and future trends, gaps, challenges and opportunities. This research will attempt to provide insight into key capabilities of the current and potential future approaches and will present a framework to better understand NH3 research with the use of in - situ as well as remote sensors in detecting NH3 in the ambient atmosphere.

  9. Automated clean-up, separation and detection of polycyclic aromatic hydrocarbons in particulate matter extracts using a 2D-LC/2D-GC system: a method translation from two FIDs to two MS detectors.

    Science.gov (United States)

    Lim, Hwanmi; Ahmed, Trifa M; Bergvall, Christoffer; Westerholm, Roger

    2017-07-24

    An online two-dimensional (2D) liquid chromatography/2D gas chromatography system with two mass-selective detectors has been developed on the basis of a previous system with two flame ionization detectors. The method translation involved the change of carrier gas from hydrogen to helium, column dimension and detectors. The 2D system with two mass-selective detectors was validated with use of polycyclic aromatic hydrocarbon (PAH) standards and two standard reference materials from air and diesel exhaust. Furthermore, the system was applied to a real sample, wood smoke particulates. The PAH values determined correlated well with the previous data and those from the National Institute of Standards and Technology. The system enhanced the benefits of the previous system, which were limited by the low detectability and lack of mass selectivity. This study shows an automated 2D system that is valid for PAH analysis of complex environmental samples directly from crude extracts. Graphical Abstract Schematic illustration showing on-line clean-up, separation and detection using 2D-LC/2D-GC/MS.

  10. 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…

  11. Improved efficiency of extraction of polycyclic aromatic hydrocarbons (PAHs) from the National Institute of Standards and Technology (NIST) Standard Reference Material Diesel Particulate Matter (SRM 2975) using accelerated solvent extraction.

    Science.gov (United States)

    Masala, Silvia; Ahmed, Trifa; Bergvall, Christoffer; Westerholm, Roger

    2011-12-01

    The efficiency of extraction of polycyclic aromatic hydrocarbons (PAHs) with molecular masses of 252, 276, 278, 300, and 302 Da from standard reference material diesel particulate matter (SRM 2975) has been investigated using accelerated solvent extraction (ASE) with dichloromethane, toluene, methanol, and mixtures of toluene and methanol. Extraction of SRM 2975 using toluene/methanol (9:1, v/v) at maximum instrumental settings (200 °C, 20.7 MPa, and five extraction cycles) with 30-min extraction times resulted in the following elevations of the measured concentration when compared with the certified and reference concentrations reported by the National Institute of Standards and Technology (NIST): benzo[b]fluoranthene, 46%; benzo[k]fluoranthene, 137%; benzo[e]pyrene, 103%; benzo[a]pyrene, 1,570%; perylene, 37%; indeno[1,2,3-cd]pyrene, 41%; benzo[ghi]perylene, 163%; and coronene, 361%. The concentrations of the following PAHs were comparable to the reference values assigned by NIST: indeno[1,2,3-cd]fluoranthene, dibenz[a,h]anthracene, and picene. The measured concentration of dibenzo[a,e]-pyrene was lower than the information value reported by the NIST. The measured concentrations of other highly carcinogenic PAHs (dibenzo[a,l]pyrene, dibenzo[a,i]pyrene, and dibenzo[a,h]pyrene) in SRM 2975 are also reported. Comparison of measurements using the optimized ASE method and using similar conditions to those applied by the NIST for the assignment of PAH concentrations in SRM 2975 indicated that the higher values obtained in the present study were associated with more complete extraction of PAHs from the diesel particulate material. Re-extraction of the particulate samples demonstrated that the deuterated internal standards were more readily recovered than the native PAHs, which may explain the lower values reported by the NIST. The analytical results obtained in the study demonstrated that the efficient extraction of PAHs from SRM 2975 is a critical requirement for the

  12. 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.

  13. 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.

    Science.gov (United States)

    Sioud, Salim; Amad, Ma'an; Al-Talla, Zeyad A

    2012-06-30

    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. 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. 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. 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 ≤4 ppm. Copyright © 2012 John Wiley & Sons, Ltd.

  14. Understanding the Impacts of Land Uses on the Source Apportionment of Atmospheric Contamination By Polycyclic Aromatic Hydrocarbons throughout a Small State in the Northeast United States

    Science.gov (United States)

    Schifman, L. A.; Boving, T. B.

    2014-12-01

    Polycyclic aromatic hydrocarbons (PAH) are ubiquitous contaminants that enter the environment through combustion processes and are often found in higher concentration of urban areas. However, once released, these compounds can travel long distances via transport through the atmosphere and can be deposited on the landscape far away from their original source. This PAH deposition pattern can slowly lead to the diffuse contamination of whole landscapes. Since most of the air masses entering the northeastern United States originate from the Midwest where coal burning power plants are plentiful, several atmospheric pollutants are introduced to the region in addition to local sources. Here, atmospheric deposition of PAHs in six different locations throughout Rhode Island was measured using passive bulk-deposition samplers for 3 years. The data were analyzed statistically by principal component analysis and factor analysis to identify the source of contamination and respective apportionment. The data clearly show that an urban-to- rural gradient exists where deposition rates are significantly higher in urban areas (up to 12325 ng/d m2 ∑PAH) compared to rural areas (as low as 11 ng/d m2 ∑PAH) and also follow seasonal trends that show higher deposition rates in the fall and winter compared to the summer and spring time. Further, based on PAH source apportionment ratios, contamination origins differ spatially. For example, fossil fuel, coal, and vehicle combustion is present in all samples; however fossil fuel combustion is dominant in urban samples. In Rural areas biomass combustion is much more prevalent and is not as greatly represented in urban or suburban areas. Therefore, even in a small state such as Rhode Island airborne PAH contamination can be fingerprinted readily for different sampling areas, indicating that distant emission sources have a widespread impact on regional air quality.

  15. The Effects of Particle Size, Relative Humidity, and Sulfur Dioxide on Iron Solubility in Atmospheric Particulate Matter

    Science.gov (United States)

    Cartledge, B. T.; Marcotte, A.; Anbar, A. D.; Herckes, P.; Majestic, B. J.

    2014-12-01

    The current study focuses on studying how iron (Fe) solubility is affected by particle size, relative humidity, and exposure to sulfur dioxide (SO2). Fe, the most abundant transition metal in atmospheric particulate matter, plays a critical role in the atmospheric sulfur cycle and is a micronutrient for phytoplankton in remote regions of the ocean. To mimic oceanic particles, iron-containing minerals (hematite, magnetite, goethite, and illite) were resuspended with sodium chloride and size-segregated on Teflon filters into five different size fractions: 10-2.5 μm, 2.5-1.0 μm, 1.0-0.5 μm, 0.5-0.25 μm, and 80%) and arid environment humidity (24%). Trials with no SO2 ­were also performed as comparisons. Total Fe was determined by using microwave-assisted acid digestion and soluble Fe was determined by extracting the samples in a simulated cloud water buffer (pH 4.25, 0.5 mM acetate, 0.5 mM formate, and 0.2 mM ammonium nitrate). Both total and soluble Fe concentrations were determined via inductively-coupled plasma mass spectrometry (ICP-MS). We found that, as particle size decreased, Fe percent solubility increased for hematite, magnetite, and goethite. The percent solubility of Fe in these mineral phases steadily increased from 0.5-10% as particle size decreased. In contrast, the Fe percent solubility in illite was relatively constant for the largest four size fractions but increased dramatically in the smallest size fraction. The percent solubility of Fe in illite ranged from 5-20% as the particle size decreased. Additionally, increased Fe solubility was linked to increased relative humidity with higher percent solubility generally observed in all mineral phases for the samples exposed at the higher humidity. No correlation was observed for the effects of the SO2 on Fe percent solubility. The likely lack of Fe-SO2 interactions were also supported by synchrotron-based x-ray spectroscopy. These results help further the knowledge of how the solubilization of

  16. 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.

  17. Characterization of atmospheric particulate and metallic elements at Taichung Harbor near Taiwan Strait during 2004-2005.

    Science.gov (United States)

    Fang, Guor-Cheng; Wu, Yuh-Shen; Lin, Jum-Bo; Lin, Chi-Kwong; Rau, Jui-Yeh; Huang, Shih-Han

    2006-06-01

    Air aerosol samples for TSP (total suspended particulate), coarse particulate (particle matter with aerodynamical diameter 2.5-10 microm, PM(2.5-10)), fine particulate (particle matter with aerodynamical diameter metallic elements were collected during March 2004 to January 2005 at TH (Taichung Harbor) in central Taiwan. The seasonal variation average concentration of TSP (total suspended particulate), coarse particulate (particle matter with aerodynamical diameter 2.5-10 microm, PM(2.5-10)) and fine particulate (particle matter with aerodynamical diameter metallic elements Cu, Mn, Zn and Fe in the TSP (total suspended particulate) shows that higher concentration was observed during spring. Seasonal variation of metallic elements Pb, Cr and Mg in the TSP (total suspended particulate) shows that higher concentration was observed during winter. The average metallic element TSP (total suspended particulate) concentration order was Fe>Zn>Mg>Cu>Cr>Mn>Pb in spring. In addition, at the TH sampling site, the average concentration variation of TSP (total suspended particulate) displayed the following order: spring>winter>autumn>summer. However, the average concentration variation of coarse particulate (particle matter with aerodynamical diameter 2.5-10 microm, PM(2.5-10)) displayed the following order: spring>winter>summer>autumn. Finally, the average concentration variations of fine particulate (particle matter with aerodynamical diameter spring>summer>autumn at the TH sample site.

  18. 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.

  19. Shipboard and ground measurements of atmospheric particulate mercury and total mercury in precipitation over the Yellow Sea region.

    Science.gov (United States)

    Nguyen, Duc Luong; Kim, Jin Young; Shim, Shang-Gyoo; Ghim, Young Sung; Zhang, Xiao-Shan

    2016-12-01

    The first ever shipboard measurements for atmospheric particulate mercury (Hg(p)) over the Yellow Sea and ground measurements for atmospheric Hg(p) and total mercury (THg) in precipitation at the remote sites (Deokjeok and Chengshantou) and the urban sites (Seoul and Ningbo) surrounding the Yellow Sea were carried out during 2007-2008. The Hg(p) regional background concentration of 56.3 ± 55.6 pg m -3 over the Yellow Sea region is much higher than the typical background concentrations of Hg(p) in terrestrial environments (mercury emission sources from East Asia. The episodes of highly elevated Hg(p) concentrations at the Korean remote site were influenced through long-range transport from source regions in the Liaoning Province - one of China's most mercury-polluted regions and in the western region of North Korea. Interestingly, wet scavenging of atmospheric Hg(p) is the predominant mechanism regulating concentration of THg in precipitation at the Chinese sites; whereas, wet scavenging of gaseous oxidized mercury (GOM) might play the more important role than that of Hg(p) at the Korean sites. The highest annual wet and dry deposition fluxes of Hg were found at the Ningbo site. The comparison between wet and dry deposition fluxes suggested that dry deposition might play the more important role than wet deposition in Chinese urban areas (source regions); whereas, wet deposition is more important in Korean areas (downwind regions). Copyright © 2016 Elsevier Ltd. All rights reserved.

  20. Human health risk exposure with respect to particulate-bound polycyclic aromatic hydrocarbons at mine fire-affected coal mining complex.

    Science.gov (United States)

    Roy, Debananda; Seo, Yong-Chil; Sinha, Sweta; Bhattacharya, Abir; Singh, Gurdeep; Biswas, Pallab Kr

    2017-05-27

    Particulate-bound poly-aromatic hydrocarbons (PAHs) are of great concern due to their mutagenicity and carcinogenicity effect on human health. In this context, identification, quantification and inhalation cancer risk (ICR) assessment due to PM10- and PM2.5-bound PAHs has been carried out at six monitoring stations in a critically polluted Jharia coalfield/Dhanbad City. Identification of pollution sources at study area has been performed by using PCA statistical methods. Air quality index (AQI) and air quality health index (AQHI) were calculated based on the concentration levels of PM10. Location-wise direct comparison between AQI, AQHI and ICR was performed to analyse the risk levels. Consequently, maximum concentration levels of particulate (PM2.5 and PM10)-bound total PAHs (400 and 482 ng/m(3)) were recorded at the monitoring station Lodna Thana, followed by Bank More and Sijua Stadium, respectively. It was also observed that mine fire-affected station Lodna Thana was exaggerated with presence of PAHs due to wood and open coal burning activities. Moreover, about 1000 and 889 cases of inhalation cancer risk were estimated due to direct exposure of PM10- and PM2.5-bound PAHs in the study area, respectively. Active mine fire-affected station Lodna Thana was recorded with maximum probability of lung tumour due to inhalation cancer risk. This study has reported higher AQHI at station Dugdha Basti, Lodna Thana and Bank More, which results increased number of tumours due to ICR. This result concludes that Jharia coalfield/Dhanbad City are not only critically polluted area but it is also an inhalation cancer prone area due to direct exposure of active mine fire.

  1. 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

    2012-01-03

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

  2. Particle size distributions and elemental composition of atmospheric particulate matter in southern Italy.

    Science.gov (United States)

    Sprovieri, Francesca; Pirrone, Nicola

    2008-06-01

    Three 2-wk seasonal field campaigns were performed in 2003 and 2004 at a sampling site on the southern Tyrrhenian coast of Italy with the aim to investigate the dynamics and characteristics of particle-bound pollutants in the Mediterranean area. Fine (PM(2.5)) and coarse particulate matter (PM(10-2.5)) size fractions were collected by a manual dichotomous sampler on 37-mm Teflon filters over a 24-hr sampling period. On average, 70% of the total PM(10) (PM(2.5) + PM(10-2.5)) mass was associated with the coarse fraction and 30% with the fine fraction during the three campaigns. The ambient concentrations of Pb, Ni, Cr, Zn, Mn, V, Cd, Fe, Cu, Ca, and Mg associated with both size fractions were determined by atomic absorption spectrometry. Ambient concentrations showed differences in their absolute value, ranging from few ng x m(-3) to microg x m(-3), as well as in their variability within the PM(2.5) and PM(10-2.5) size fractions. PM(10) levels were well below the European Union (EU) limit value during the study period with the exception of three events during the first campaign (fall) and five events during the third campaign (spring). Two main sources were identified as the major contributors including mineral dust, transported from North Africa, and sea spray from the Tyrrhenian Sea. Comparing the results with backward trajectories, calculated using the Hybrid Single-Particle Lagrangian Integrated Trajectory Model (HYSPLIT) and Total Ozone Mapping Spectrometer-National Aeronautics and Space Administration (TOMS-NASA) maps, it was observed that in central and eastern Europe, the Tyrrhenian Sea and North Africa were the major emission source regions that affected the temporal variations and daily averages of PM(2.5) and PM(10-2.5) concentrations.

  3. Fast analysis of 29 polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs with ultra-high performance liquid chromatography-atmospheric pressure photoionization-tandem mass spectrometry

    Science.gov (United States)

    Lung, Shih-Chun Candice; Liu, Chun-Hu

    2015-01-01

    Polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs are ubiquitous in the environment. Some of them are probable carcinogens and some are source markers. This work presents an ultra-high performance liquid chromatography-atmospheric pressure photoionization-tandem mass spectrometry (UHPLC-APPI-MS/MS) method for simultaneous analysis of 20 PAHs and nine nitro-PAHs. These compounds are separated in 15 minutes in the positive mode and 11 minutes in the negative mode, one half of GC/MS analysis time. Two pairs of precursor/product ions are offered, which is essential for confirmation. This method separates and quantifies benzo[a]pyrene (the most toxic PAHs) and non-priority benzo[e]pyrene (isomers, little toxicity) to avoid overestimation of toxin levels, demonstrating its importance for health-related researches. With 0.5% 2,4-difluoroanisole in chlorobenzene as the dopant, limits of detection of PAHs except acenaphthylene and those of nitro-PAHs except 2-nitrofluoranthene are below 10 pg and 3 pg, respectively, mostly lower than or comparable to those reported using LC-related systems. The responses were linear over two orders of magnitude with fairly good accuracy and precision. Certified reference materials and real aerosol samples were analyzed to demonstrate its applicability. This fast, sensitive, and reliable method is the first UHPLC-APPI-MS/MS method capable of simultaneously analyzing 29 environmentally and toxicologically important PAHs and nitro-PAHs. PMID:26265155

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

    Science.gov (United States)

    Callén, M S; López, J M; Iturmendi, A; Mastral, A M

    2013-12-01

    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 (R(2) = 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. Copyright © 2012 Elsevier Ltd. All rights reserved.

  5. Monitoring of atmospheric particulate matter around sources of secondary inorganic aerosol

    Science.gov (United States)

    Alastuey, A.; Querol, X.; Rodríguez, S.; Plana, F.; Lopez-Soler, A.; Ruiz, C.; Mantilla, E.

    2004-09-01

    A physicochemical characterisation of airborne particulate matter (PM) was performed in a region affected by the emissions from a source of precursors of secondary inorganic aerosols (SIA, 1050 MW power plant). This characterisation sought to study the interferences of other possible natural and anthropogenic sources when monitoring PM10, PM2.5 and PM1 around this emission source. The study was performed in the semi-arid Ebro basin and Catalan and Iberian ranges (Eastern Spain) and consisted in (1) monitoring the transport and impacts on the ground of the SO2 plume (fumigation), (2) chemically characterising (25 PM components) of TSP-size fractions, and diurnal and nocturnal PM10 and PM2.5 samples, and (3) in measuring the PM mass size distribution. This PM characterisation was undertaken in ambient air, during fumigations of the SO2 plume on the ground and around other local PM sources. PM1 was found to be the best parameter for monitoring PM pollution derived from the SO2 emissions owing to the formation of ammonium-sulphate in the finest PM fractions. Three PM1 & PM2.5 events were recorded during the field measurement campaign: two events were caused by ammonium-sulphate episodes, the third was due to an African dust outbreak. PM-mass size distribution and the high correlation of PM1 with SO2 during the SO2 fumigation events suggest that a significant fraction of sulphate is formed by means of `new particle formation' processes (nucleation). PM10 presents a much higher variability (noise) than PM1 & PM2.5 owing to the re-suspension of coarse (2.5- 10 μm) mineral dust particles. The PM1 load in PM10 undergoes significant variations: 60-80% during plume fumigations, 20-60% in ambient air, and down to 10% in areas affected by mineral dust re-suspension. The daily cycles observed in some PM components (sulphate, nitrate and mineral dust elements) and the chemical features of PM are also described in detail.

  6. Atmospheric pollution; Pollution atmospherique

    Energy Technology Data Exchange (ETDEWEB)

    Lambrozo, J.; Guillossou, G. [EDF-Gas de France, Service des Etudes Medicales, 75 - Paris (France)

    2008-10-15

    The atmosphere is the reservoir of numerous pollutants (nitrogen oxides, sulfur oxides, carbon oxides, particulates, volatile organic compounds, polycyclic aromatic hydrocarbons) from natural origin or anthropogenic origin ( industry, transport, agriculture, district heating). With epidemiologic studies the atmospheric pollution is associated with an increase of respiratory and cardiovascular diseases. At the european level, the technological progress, the legislation have allowed a reduction of pollutant emissions, however these efforts have to be continued because the sanitary impact of atmospheric pollution must not be underestimated, even if the risks appear less important that these ones in relation with tobacco, inside pollution or others factors of cardiovascular risks. Indeed, on these last factors an individual action is possible for the exposure to air pollution people have no control. (N.C.)

  7. 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.

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

    Science.gov (United States)

    Li, Wei; Wang, Chen; Wang, Hongqijie; Chen, Jiwei; Yuan, Chenyi; Li, Tongchao; Wang, Wentao; Shen, Huizhong; Huang, Ye; Wang, Rong; Wang, Bin; Zhang, Yanyan; Chen, Han; Chen, Yuanchen; Tang, Jianhui; Wang, Xilong; Liu, Junfeng; Coveney, Raymond M; Tao, Shu

    2014-02-01

    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/m(3), 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. Copyright © 2013 Elsevier Ltd. All rights reserved.

  9. Hydride generation atomic fluorescence spectrometric determination of As, Bi, Sb, Se(IV) and Te(IV) in aqua regia extracts from atmospheric particulate matter using multivariate optimization

    Energy Technology Data Exchange (ETDEWEB)

    Moscoso-Perez, Carmen [Department of Analytical Chemistry, Faculty of Sciences, University of A Coruna, Campus da Zapateira s/n, E-15071 A Coruna (Spain); Moreda-Pineiro, Jorge [Department of Analytical Chemistry, Faculty of Sciences, University of A Coruna, Campus da Zapateira s/n, E-15071 A Coruna (Spain)]. E-mail: jmoreda@udc.es; Lopez-Mahia, Purificacion [Department of Analytical Chemistry, Faculty of Sciences, University of A Coruna, Campus da Zapateira s/n, E-15071 A Coruna (Spain); Muniategui-Lorenzo, Soledad [Department of Analytical Chemistry, Faculty of Sciences, University of A Coruna, Campus da Zapateira s/n, E-15071 A Coruna (Spain); Fernandez-Fernandez, Esther [Department of Analytical Chemistry, Faculty of Sciences, University of A Coruna, Campus da Zapateira s/n, E-15071 A Coruna (Spain); Prada-Rodriguez, Dario [Department of Analytical Chemistry, Faculty of Sciences, University of A Coruna, Campus da Zapateira s/n, E-15071 A Coruna (Spain)

    2004-11-22

    A highly sensitive and simple method, based on hydride generation and atomic fluorescence detection, has been developed for the determination of As, Bi, Sb, Se(IV) and Te(IV) in aqua regia extracts from atmospheric particulate matter samples. Atmospheric particulates matter was collected on glass fiber filters using a medium volume sampler (PM1 particulate matter). Two-level factorial designs have been used to optimise the hydride generation atomic fluorescence spectrometry (HG-AFS) procedure. The effects of several parameters affecting the hydride generation efficiency (hydrochloric acid, sodium tetrahydroborate and potassium iodide concentrations and flow rates) have been evaluated using a Plackett-Burman experimental design. In addition, parameters affecting the hydride measurement (delay, analysis and memory times) have been also investigated. The significant parameters obtained (sodium tetrahydroborate concentration, sodium tetrahydroborate flow rate and analysis time for As; hydrochloric acid concentration and sodium tetrahydroborate flow rate for Se(IV); and sodium tetrahydroborate concentration and sodium tetrahydroborate flow rate for Te(IV)) have been optimized by using 2{sup n} + star central composite design. Hydrochloric acid concentration and sodium tetrahydroborate flow rate were the significant parameters obtained for Sb and Bi determination, respectively. Using a univariate approach these parameters were optimized. The accuracy of methods have been verified by using several certified reference materials: SRM 1648 (urban particulate matter) and SRM 1649a (urban dust). Detection limits in the range of 6 x 10{sup -3} to 0.2 ng m{sup -3} have been achieved. The developed methods were applied to several atmospheric particulate matter samples corresponding to A Coruna city (NW Spain)

  10. 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...

  11. Organic content of particulate matter in the atmosphere of Quargla City, Algeria

    Energy Technology Data Exchange (ETDEWEB)

    Yassaa, N. [University of Sciences and Technology, Institute of Chemistry, Laboratoire d' Analyse Organique Fonctionelle, El-Alia (Algeria); Meklati, B.Y. [Centre de Recherche Scientifique et Technique en Analyses Physico-Chimiques, Algier (Algeria); Cecinato, A.; Marino, F.; Balducci, C. [Consiglio Nazionale delle Ricerche, Istituto sull' Inquinamento Atmosferico, Area della Ricerca di Roma, Monterotondo Scalo, RM (Italy)

    2001-10-01

    The particle-bound organic compounds comprising n-alkanes, n-alkanoic monocarboxylic acids, polynuclear aromatic hydrocarbons (PAH) and nitrated polynuclear aromatic hydrocarbons (NPAH) were investigated in ambient air of the Quargla city area (Algeria) during a short campaign performed in November 1999. The distribution profile of n-alkanes was consistent with the petrogenic origin of aerosols, suggesting that they were related to torching processes of crude oil refuses in the petroleum extraction field located not far from Quargla. Instead, the presence of n-alkanoic acids of low molecular weight was indicative of microbial activity experienced by the site. PAH levels were low when compared to other polluted areas. The presence of 2-nitrofluoranthene and 2-nitropyrene, which can result from in-situ nitration of fluoranthene and pyrene, was concurrent with the substantial depletion of the most reactive among PAH, suggesting that photochemical processes influence the composition of the Saharian atmosphere. [Italian] Una breve campagna di monitoraggio e' stata eseguita nell'area di Quargla (citta' dell'entroterra algerino) al fine di investigare la composizione degli aerosoli organici dell'atmosfera. Sono stati identificati e valutati gli n-alcani, gli acidi alcanoici mono-carbossilici, gli idrocarburi policiclici aromatici (PAH) ed i PAH nitrati (NPAH). La composizione della frazione alifatica era compatibile con l'origine petrogenica degli aerosoli, concordando con quella caratteristica dei pennacchi fumosi ai pozzi petroliferi di un vicino campo di estrazione. La presenza degli omologhi leggeri tra gli acidi n-alcanoici (fino a C{sub 1}8) era indicativa di attivita' microbica. I PAH mostravano concentrazioni in aria inferiori a quelle di aree inquinate. La presenza di 2-nitrofluorantene e 2-nitropirene, di origine almeno parzialmente fotochimica, contemporanea alla scomparsa dei piu' reattivi tra i PAH, indica che la

  12. Long-term trends (1990-2014), health risks, and sources of atmospheric polycyclic aromatic hydrocarbons (PAHs) in the U.S.

    Science.gov (United States)

    Liu, Bian; Xue, Zhuqing; Zhu, Xianlei; Jia, Chunrong

    2017-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are a category of over 100 various chemicals released from numerous combustion sources. The ubiquity and toxicity of PAHs have posed high health risks on human populations. This study aims to examine the long-term trends of atmospheric PAHs at the national-level in the U.S., and evaluate their cancer risks. Daily concentrations of PAHs measured at 169 monitoring stations between 1990 and 2014 were obtained from the U.S. Environmental Protection Agency's Air Quality System. Temporal trends were examined using generalized linear model with generalized estimating equations. Random-effects analysis of variance was performed to explore variance between regions, sites, years, and months with a hierarchical structure. Source categories were identified using diagnostic ratios. National population level cancer risks were estimated using the relative potency factors and inhalation unit risk method. Ambient PAH concentrations displayed an overall downward trend (6-9% annual reduction) in urban areas, but not in rural areas. Seasonal and weekday/weekend effects were significant. Urban concentrations were twice of the rural level. The between-site variation outweighed the temporal variation, indicating large spatial heterogeneity. The predominant PAH sources were from traffic and non-traffic related fuel combustions with a dominant contribution from diesel emissions. The average excess lifetime cancer risk was estimated to be 9.3 ± 30.1 × 10-6 (GM: 4.2 × 10-6) from exposure to ten carcinogenic PAHs. This is the first comprehensive study of the spatiotemporal trends of ambient PAHs at the U.S. national level. The results indicate that future efforts aimed to reduce PAH exposures should focus on diesel emission controls and extending the geographic coverage of air monitoring. Copyright © 2016 Elsevier Ltd. All rights reserved.

  13. Dispersion of atmospheric fine particulate matters in simulated lung fluid and their effects on model cell membranes.

    Science.gov (United States)

    Zhou, Qiuhua; Wang, Lixin; Cao, Zhaoyu; Zhou, Xuehua; Yang, Fan; Fu, Pingqing; Wang, Zhenhua; Hu, Jingtian; Ding, Lei; Jiang, Wei

    2016-01-15

    Atmospheric fine particulate matter (PM2.5) was collected to investigate its dispersion in simulated lung fluid (SLF) and its interaction with model cell membranes. Organic acids, NH4(+), SO4(2-) and NO3(-) were detected in PM2.5 soluble fraction, and heavy metals were detected from the total mass. The insoluble fraction contained kaolinite, CaCO3, aliphatic carbons, aromatic rings, carboxyl and hydroxyl groups reflected by the infrared spectra. Proteins dispersed PM2.5 in SLF, resulted in smaller hydrodynamic diameter (dH) and slower sedimentation rate. Conversely, phospholipids increased dH value and accelerated sedimentation rate. Giant unilamellar vesicles (GUVs) and supported lipid bilayers (SLBs) were used as model cell membranes. PM2.5 adhered on and disrupted the membrane containing positively-charged lipids but not the membrane containing neutrally- and negatively-charged lipids, which was monitored by microscopy and a quartz crystal microbalance with dissipation (QCM-D). The cationic sites on membrane were necessary for PM2.5 adhesion, but membrane should be disrupted by the combined action of electrostatic forces and hydrogen bonds between PM2.5 oxygen containing groups and the lipid phosphate groups. Our results specified the roles of proteins and phospholipids in PM2.5 dispersion and transport, highly suggested that the health hazard of PM2.5 was related to the biomolecules in the lung fluid and the particle surface groups. Copyright © 2015 Elsevier B.V. All rights reserved.

  14. An estimate of the global burden of anthropogenic ozone and fine particulate matter on premature human mortality using atmospheric modeling.

    Science.gov (United States)

    Anenberg, Susan C; Horowitz, Larry W; Tong, Daniel Q; West, J Jason

    2010-09-01

    Ground-level concentrations of ozone (O3) and fine particulate matter [model simulations of preindustrial and present-day (2000) concentrations to derive exposure estimates. Attributable mortalities were estimated using health impact functions based on long-term relative risk estimates for O3 and PM2.5 from the epidemiology literature. Using simulated concentrations rather than previous methods based on measurements allows the inclusion of rural areas where measurements are often unavailable and avoids making assumptions for background air pollution. Anthropogenic O3 was associated with an estimated 0.7 +/- 0.3 million respiratory mortalities (6.3 +/- 3.0 million years of life lost) annually. Anthropogenic PM2.5 was associated with 3.5 +/- 0.9 million cardiopulmonary and 220,000 +/- 80,000 lung cancer mortalities (30 +/- 7.6 million years of life lost) annually. Mortality estimates were reduced approximately 30% when we assumed low-concentration thresholds of 33.3 ppb for O3 and 5.8 microg/m3 for PM2.5. These estimates were sensitive to concentration thresholds and concentration-mortality relationships, often by > 50%. Anthropogenic O3 and PM2.5 contribute substantially to global premature mortality. PM2.5 mortality estimates are about 50% higher than previous measurement-based estimates based on common assumptions, mainly because of methodologic differences. Specifically, we included rural populations, suggesting higher estimates; however, the coarse resolution of the global atmospheric model may underestimate urban PM(2.5) exposures.

  15. 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.

  16. Eco-toxicological bioassay of atmospheric fine particulate matter (PM2.5) with Photobacterium Phosphoreum T3.

    Science.gov (United States)

    Wang, Wenxin; Shi, Chanzhen; Yan, Yan; Yang, Yunfei; Zhou, Bin

    2016-11-01

    A bioluminescent bacterium, Photobacterium phosphoreum T3 (PPT3), was used as a bio-indicator for the atmospheric fine particulate matter (PM2.5) to determine the eco-toxicity of PM2.5. The PM2.5 contains toxic chemicals, which reduce light output. The PM2.5 samples were collected in the period from March 2014 to January 2015 in Nanjing and analyzed for the chemical composition versus their eco-toxicity. The eco-toxicological responses of each toxicant were detected in PM2.5 samples with PPT3. The dose-response curves obtained were verified using the Weibull fitting function. According to the measured EC50 values (EC50, the concentration of a toxicant that inhibits 50% of the bioluminescence), the toxicity sequence was: B[a]P>hexa-PCB>tetra-PCB>tri-PCB>Pb(2+)>DEHP>Cu(2+)>DBP>BDE209>Zn(2+)>DMP>DEP, where B[a]P is benzo(a)pyrene, PCB is polychlorinated biphenyl, DEHP is diethylhexyl phthalate, DBP is dibutyl phthalate, BDE209 is decabromodiphenyl ether, DMP is dimethyl phthalate, and DEP is diethyl phthalate. All the PM2.5 samples analyzed proved to be weak toxic for PPT3. The toxicity of PM2.5 was assessed by the dose-addition of organic species and heavy metallic elements existing in PM2.5 with PPT3. The bioluminescence test showed that the metals and organics detected in PM2.5 promoted PM2.5 toxicity. The total detectable organics (denoted by ΣOrs) exhibited slightly higher toxicity than the total metals (denoted by ΣMs). In contrast, the sum of water-soluble ions (denoted by ΣIons) was beneficial to PPT3. The PM2.5 toxicity increased as the PM2.5 trapped more organics or metallic elements from the industrial or densely populated urban areas, where the PM2.5 had a high inhibition rate of bioluminescence for PPT3 in contrast to the residential PM2.5 samples, where the minimum inhibition rate was observed. The toxicity of PM2.5 samples varied with the mass concentrations, chemical constituents, and sampling locations. The chemicals in PM2.5, especially organic

  17. Size distributions and formation of ionic species in atmospheric particulate pollutants in Beijing, China: 1—inorganic ions

    Science.gov (United States)

    Yao, Xiaohong; Lau, Arthur P. S.; Fang, Ming; Chan, Chak K.; Hu, Min

    To study the formation of atmospheric sulfate, nitrate and chloride particulates in Beijing, China, 14 sets of measurements of the concentrations of SO 2, HNO 3, NH 3 and size-segregated particles were made in the summer of 2001 and the spring of 2002. Because of the very different humidity levels in Beijing in the summer and the spring, significant differences in the size characteristics and in the formation mechanisms of these ions were found. In the summer, the major fraction of sulfate was present in the fine mode with a mass median aerodynamic diameter (MMAD) of 0.7±0.1 μm. Its formation was attributed to in-cloud processing, which was supported by the observation of a large mole ratio of the sulfate at 0.54-1.0 μm to SO 2, with a maximum value of 3.0. The major fraction of nitrate sometimes appeared in the fine mode with an MMAD of 0.7±0.1 μm and sometimes in the coarse mode with an MMAD of 6.0±1.5 μm. The coarse mode nitrate was associated with Ca 2+. The major peak of chloride, in most cases, appeared in the coarse mode. Chloride was expected to have formation mechanisms similar to nitrate formation in the coarse mode. In the spring, the major fraction of sulfate was present in the fine mode with an MMAD of 0.45±0.05 μm and its formation was ascribed to non-cloud heterogeneous processes. A small mole ratio of the fine mode sulfate to SO 2, with a maximum value of only 0.06, was observed. Nitrate and chloride generally have a similar MMAD as sulfate in the fine mode, suggesting that both may originate from atmospheric processes similar to sulfate formation. Alternatively, they could be formed by gas condensation onto existing sulfate particles. Overall, much more efficient sulfate formation by cloud processing led to a higher sulfate concentration in the summer than in the spring, although the SO 2 concentration followed the reverse trend in Beijing.

  18. Distribution and partitioning of aliphatic hydrocarbons and polycyclic aromatic hydrocarbons between water, suspended particulate matter, and sediment in harbours of the West coastal of the Gulf of Tunis (Tunisia).

    Science.gov (United States)

    Mzoughi, Nadia; Chouba, Lassaad

    2011-03-01

    Harbours of La Goulette, Rades and Sidi Bou Said are considered as the principal largest and most important port in the Gulf of Tunis characterised by a direct influence of different activities (sailing, industry and fishing) to the Mediterranean Sea. Due to their social and economic impact, a comprehensive assessment of the spatial distribution and partitioning of 24 polycyclic aromatic hydrocarbons (PAHs) and 18 aliphatic hydrocarbons (AHs) in summer and in winter among overlying water, suspended particulate matter (SPM) and surface sediments is essential. Distribution of hydrophobic organic contaminants in abiotic compartments is important for describing their transfer and fate in aquatic ecosystems and to identify the potential danger due to mobilization of contaminants produced by managing of the same sediments. Total organic carbon (TOC) contents range between 4.3% and 6.5%, with an average value of 5.9% in summer, and between 2.3% and 9.6%, with an average value of 6.1% in winter. The average concentrations of ΣPAH in winter and in summer were respectively 703.1 ng L⁻¹ and 378.4 ng L⁻¹ in seawater, 4599.1 ng g⁻¹ and 3114 ng g⁻¹ in SPM, and 1507.6 ng g⁻¹ dw (dry weight) and 1294.6 ng g⁻¹ dw in surface sediment. For ΣAH the average concentrations in winter and in summer were respectively 701 ng L⁻¹ and 741.7 ng L⁻¹ in seawater, 6743.5 ng g⁻¹ and 6282.9 ng g⁻¹ in SPM, and 4971.3 ng g⁻¹ and 4588.1 ng g⁻¹ in surface sediment. Higher PAH and AH concentrations were observed in SPM than in surface sediment. SPM and water were dominated by PAH with low molecular weight, while for sediment low and high molecular weight PAHs were present. PAH and AH fingerprint ratios, such as pristane to phytane (Pr/Ph), phenanthrene to anthracene (Phe/An) and fluoranthene to pyrene (Fl/Py), suggest that hydrocarbons in all harbours may originate from both pyrolytic and petrogenic sources derived from discharge of untreated sewage and wastewater

  19. Simulation of the evolution of particle size distributions containing coarse particulate in the atmospheric surface layer with a simple convection-diffusion-sedimentation model

    Science.gov (United States)

    Hubbard, J. A.; Haglund, J. S.; Ezekoye, O. A.

    The Fugitive Dust Model (FDM) and Industrial Source Complex (ISC), widely used coarse particulate dispersion models, have been shown inaccurate due to the neglect of vertical variations in atmospheric wind speed and turbulent diffusivity (Vesovic et al., 2001), omission of the gravitational advection velocity, and an underestimation of the ground deposition velocity (Kim and Larson, 2001). A simple, transient two-dimensional convection-diffusion-sedimentation model is proposed to simulate the evolution in particle size distribution of an aerosol 'puff' containing coarse particulate in the atmospheric surface layer. Monin-Okhubov similarity theory, accompanied by empirical observations made by Businger et al. (1971), is adopted to characterize the surface layer wind speed and turbulent diffusivity profiles over a wide range of atmospheric conditions. A first order analysis of the crossing trajectories effect suggests simulation data presented here are not significantly affected by particle inertia. The model is validated against Suffield experimental data in which coarse particulate deposition was measured out to a distance of 800 m from the source (Walker, 1965). Good agreement is found for the decay in ground deposits with distance from the source for stable atmospheres. Deposition data was also simulated for unstable atmospheric stratification and the current model was determined to modestly underestimate the peak concentration with increasing accuracy further downwind of the release. The current model's effective deposition velocity was compared to that suggested by Kim et al. (2000) and shows improvement with respect to FDM. Lastly, the model was used to simulate the dispersion of nine lognormal aerosol puffs in the lowest 50 m of the atmospheric surface layer for four classes of atmospheric stability. The simulated mass median aerodynamic diameters (MMAD) at multiple downwind sampling locations were calculated and plotted with distance from the source. The

  20. CORRELATION BETWEEN PARTICULATE MATTER ...

    African Journals Online (AJOL)

    BIG TIMMY

    2017-03-21

    Mar 21, 2017 ... Measurement of atmospheric particulate matter was carried out with a view to establish the potential influence of meteorological parameters such as wind speed, wind direction, air temperature, rainfall, relative humidity and global radiation on the mass concentration. Particulate matter (PM) in two size ...

  1. 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

  2. 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

  3. Forward research on transmission characteristics of near-surface particulate-matter-polluted atmosphere in mining area combined with CFD method.

    Science.gov (United States)

    Wang, Wenzheng; Wang, Yanming; Shi, Guoqing

    2015-07-27

    The optical radiation and radiation transfer characteristics of atmospheric particulate matter (PM) in mining area of northwest China were simulated and analyzed in this paper. Computational fluid dynamics (CFD) method was adopted to simulate the distribution of PM considering the local desertification and mining activities. The 1-D radiative transfer equation was solved using discrete ordinates method combined with Mie scattering model based on the CFD simulation results. The spectral aerosol optical depth and transmission characteristics of PM polluted atmosphere in the wavelength of 1-25μm under different intensity of dust releases, wind speeds and dust compositions were obtained and analyzed. The simulation results show that: the transmission characteristics are obviously enhanced with the increase of wind speed and sand particles' proportion but greatly decreased with the increase of the intensity of dust release.

  4. 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.; Bothner, Michael H.; 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.

  5. 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.

  6. Development of a gas chromatography-mass spectrometry method for the determination of pesticides in gaseous and particulate phases in the atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Borras, E.; Sanchez, P.; Munoz, A. [Instituto Universitario Centro de Estudios Ambientales del Mediterraneo CEAM-UMH (Fundacion CEAM-UMH), 46980 Paterna, Valencia (Spain); Tortajada-Genaro, L.A., E-mail: luitorge@qim.upv.es [Instituto IDM, Departamento de Quimica, Universitat Politecnica de Valencia, Cami de Vera s/n 46022 Valencia (Spain)

    2011-08-05

    Highlights: {yields} An efficient method for the determination of sixteen pesticides in atmospheric samples. {yields} XAD-4 is an interesting support for collecting gas-phase pesticides, with similar performances than the conventional XAD-2. {yields} The ultrasonic extraction is cheaper, less aggressive and time-consuming with excellent analytical parameters. {yields} The method has been successfully tested by using high volume atmospheric simulation chamber and field campaigns. - Abstract: A reliable multi-residue method for determining gaseous and particulate phase pesticides in atmospheric samples has been developed. This method, based on full scan gas chromatography-mass spectrometry (GC-MS), allowed the proper determination of sixteen relevant pesticides, in a wide range of concentrations and without the influence of interferences. The pesticides were benfluralin, bitertanol, buprofezin, chlorfenvinphos, chlorpyrifos, chlorpyrifos-methyl, ethalfluralin, fenthion, lindane, malathion, methidathion, propachlor, propanil, pyriproxifen, tebuconazol and trifluralin. Comparisons of two types of sampling filters (quartz and glass fibre) and four types of solid-phase cartridges (XAD-2, XAD-4, Florisil and Orbo-49P) showed that the most suitable supports were glass fibre filter for particulate pesticides and XAD-2 and XAD-4 cartridges for gaseous pesticides (>95% recovery). Evaluations of elution solvents for ultrasonic-assisted extraction demonstrated that isooctane is better than ethylacetate, dichloromethane, methanol or a mixture of acetone:hexane (1:1). Recovery assays and the standard addition method were performed to validate the proposed methodology. Moreover, large simulator chamber experiments allowed the best study of the gas-particle partitioning of pesticides for testing the sampling efficiency for the validation of an analytical multiresidue method for pesticides in air. Satisfactory analytical parameters were obtained, with a repeatability of 5 {+-} 1%, a

  7. Enhanced levels of atmospheric low-molecular weight monocarboxylic acids in gas and particulates over Mt. Tai, North China, during field burning of agricultural wastes

    Science.gov (United States)

    Mochizuki, Tomoki; Kawamura, Kimitaka; Nakamura, Shinnosuke; Kanaya, Yugo; Wang, Zifa

    2017-12-01

    To understand the source and atmospheric behaviour of low molecular weight monocarboxylic acids (monoacids), gaseous (G) and particulate (P) organic acids were collected at the summit of Mt. Tai in the North China Plain (NCP) during field burning of agricultural waste (wheat straw). Particulate organic acids were collected with neutral quartz filter whereas gaseous organic acids were collected with KOH-impregnated quartz filter. Normal (C1-C10), branched (iC4-iC6), hydroxy (lactic and glycolic), and aromatic (benzoic) monoacids were determined with a capillary gas chromatography employing p-bromophenacyl esters. We found acetic acid as the most abundant gas-phase species whereas formic acid is the dominant particle-phase species. Concentrations of formic (G/P 1 570/1 410 ng m-3) and acetic (3 960/1 120 ng m-3) acids significantly increased during the enhanced field burning of agricultural wastes. Concentrations of formic and acetic acids in daytime were found to increase in both G and P phases with those of K+, a field-burning tracer (r = 0.32-0.64). Primary emission and secondary formation of acetic acid is linked with field burning of agricultural wastes. In addition, we found that particle-phase fractions (Fp = P/(G + P)) of formic (0.50) and acetic (0.31) acids are significantly high, indicating that semi-volatile organic acids largely exist as particles. Field burning of agricultural wastes may play an important role in the formation of particulate monoacids in the NCP. High levels (917 ng m-3) of particle-phase lactic acid, which is characteristic of microorganisms, suggest that microbial activity associated with terrestrial ecosystem significantly contributes to the formation of organic aerosols.

  8. Elemental and carbon isotope composition of total particulate matter in the urban atmosphere of Krakow, southern Poland: summer-winter contrast

    Science.gov (United States)

    Zimnoch, Miroslaw; Samek, Lucyna; Morawski, Filip; Rozanski, Kazimierz; Bartyzel, Jakub

    2017-04-01

    Deterioration of air quality in urban agglomerations is a growing problem of global significance [1]. This spurs research towards better understanding of parameters controlling air quality in urban environment (sources of particulate matter and gaseous contaminants, spatial and temporal variability of air quality, impact of atmospheric dynamics on the air quality, and several others). Krakow belongs to four largest cities in Poland. With nearly one million inhabitants, rapidly growing car traffic and significant industrial activities, Krakow agglomeration represents a typical urban environment in the eastern Europe. Characteristic features of the local climate are generally weak winds (annual average around 2.7 m s-1) and frequent inversions, extending sometimes over several days, particularly during winter seasons, favor accumulation of pollutants originating from surface emissions in the atmosphere over the city. Krakow ranks among the most polluted cities in Europe. There is an ongoing discussion on the role of different sources of total suspended particulate matter (TSPM) in the city's atmosphere, such as traffic, low- and high-level emissions related to burning of coal for heating purposes, resuspension of street dust, and some others. The presented work was aimed at exploring possibilities of using carbon isotope composition of total particulate matter collected in Krakow atmosphere, for better characterization of TSPM sources in the city, with the focus on seasonal changes of the character and intensity of those sources. Archived samples of TSPM deposited on filters (sampling interval between 5 and 20 days) and spanning the period 2005 - 2010 [3] were used for this purpose. For each year one pair of filters representing summer and winter conditions was selected. The work comprised also multi-elemental analysis of available TSPM samples using EDXRF technique. The measurements of 13C and 14C content in the total elemental carbon collected on filters revealed

  9. 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

  10. EPR investigations of Mn 2+, Fe 3+ ions and carbonaceous radicals in atmospheric particulate aerosols during their transport over the eastern coast of the English Channel

    Science.gov (United States)

    Ledoux, Frédéric; Zhilinskaya, Elena; Bouhsina, Saâd; Courcot, Lucie; Bertho, Marie-Laure; Aboukaı̈s, Antoine; Puskaric, Emile

    Electron paramagnetic resonance (EPR) spectroscopy was used to follow the evolution of the chemical forms of manganese and study other paramagnetic species in the atmospheric particulate aerosols at Wimereux, a French station located on the eastern coast of the English Channel. In parallel, Graphite Furnace Atomic Absorption Spectrometry (GFAAS) was used to measure the metal concentrations. Fe concentration values are common in North Sea sites, but those of Mn are quite higher due to the presence of an important local source of Mn. EPR spectra have evidenced isolated Fe 3+ and Mn 2+ ions and carbonaceous products with variable intensities according to the wind directions. Amounts of paramagnetic species and carbonaceous products are maximum for continental winds and minimum for marine winds. Three Mn types were identified depending on the sampling distance from the source of emission and the size of the particles.

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

    Science.gov (United States)

    Xu, L Y; Xie, X D; Li, S

    2013-07-01

    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. Copyright © 2013 Elsevier Ltd. All rights reserved.

  12. 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). Copyright © 2015 Elsevier Ltd. All rights reserved.

  13. Investigation into the Effect of Atmospheric Particulate Matter (PM2.5 and PM10) Concentrations on GPS Signals.

    Science.gov (United States)

    Lau, Lawrence; He, Jun

    2017-03-03

    The Global Positioning System (GPS) has been widely used in navigation, surveying, geophysical and geodynamic studies, machine guidance, etc. High-precision GPS applications such as geodetic surveying need millimeter and centimeter level accuracy. Since GPS signals are affected by atmospheric effects, methods of correcting or eliminating ionospheric and tropospheric bias are needed in GPS data processing. Relative positioning can be used to mitigate the atmospheric effect, but its efficiency depends on the baseline lengths. Air pollution is a serious problem globally, especially in developing countries that causes health problems to humans and damage to the ecosystem. Respirable suspended particles are coarse particles with a diameter of 10 micrometers or less, also known as PM10. Moreover, fine particles with a diameter of 2.5 micrometers or less are known as PM2.5. GPS signals travel through the atmosphere before arriving at receivers on the Earth's surface, and the research question posed in this paper is: are GPS signals affected by the increased concentration of the PM2.5/PM10 particles? There is no standard model of the effect of PM2.5/PM10 particles on GPS signals in GPS data processing, although an approximate generic model of non-gaseous atmospheric constituents (GPS signals and validates the aforementioned approximate model with a carrier-to-noise ratio (CNR)-based empirical method. Both the approximate model and the empirical results show that the atmospheric PM2.5/PM10 particles and their concentrations have a negligible effect on GPS signals and the effect is comparable with the noise level of GPS measurements.

  14. Investigation into the Effect of Atmospheric Particulate Matter (PM2.5 and PM10 Concentrations on GPS Signals

    Directory of Open Access Journals (Sweden)

    Lawrence Lau

    2017-03-01

    Full Text Available The Global Positioning System (GPS has been widely used in navigation, surveying, geophysical and geodynamic studies, machine guidance, etc. High-precision GPS applications such as geodetic surveying need millimeter and centimeter level accuracy. Since GPS signals are affected by atmospheric effects, methods of correcting or eliminating ionospheric and tropospheric bias are needed in GPS data processing. Relative positioning can be used to mitigate the atmospheric effect, but its efficiency depends on the baseline lengths. Air pollution is a serious problem globally, especially in developing countries that causes health problems to humans and damage to the ecosystem. Respirable suspended particles are coarse particles with a diameter of 10 micrometers or less, also known as PM10. Moreover, fine particles with a diameter of 2.5 micrometers or less are known as PM2.5. GPS signals travel through the atmosphere before arriving at receivers on the Earth’s surface, and the research question posed in this paper is: are GPS signals affected by the increased concentration of the PM2.5/PM10 particles? There is no standard model of the effect of PM2.5/PM10 particles on GPS signals in GPS data processing, although an approximate generic model of non-gaseous atmospheric constituents (<1 mm can be found in the literature. This paper investigates the effect of the concentration of PM2.5/PM10 particles on GPS signals and validates the aforementioned approximate model with a carrier-to-noise ratio (CNR-based empirical method. Both the approximate model and the empirical results show that the atmospheric PM2.5/PM10 particles and their concentrations have a negligible effect on GPS signals and the effect is comparable with the noise level of GPS measurements.

  15. Impacts of traffic emissions on atmospheric particulate nitrate and organics at a downwind site on the periphery of Guangzhou, China

    Directory of Open Access Journals (Sweden)

    Y. M. Qin

    2017-09-01

    Full Text Available Particulate matter (PM pollution on the peripheries of Chinese megacities can be as serious as in cities themselves. Given the substantial vehicular emissions in inner-city areas, the direct transport of primary PM (e.g., black carbon and primary organics and effective formation of secondary PM from precursors (e.g., NOx and volatile organic compounds can contribute to PM pollution in buffer zones between cities. To investigate how traffic emissions in inner-city areas impact these adjacent buffer zones, a suite of real-time instruments were deployed in Panyu, downwind from central Guangzhou, from November to December 2014. Nitrate mass fraction was higher on high-PM days, with the average nitrate-to-sulfate ratio increasing from around 0.35 to 1.5 as the PM mass concentration increased from 10 to 160 µg m−3. Particulate nitrate was strongly correlated with excess ammonium (([NH4+] ∕ [SO42−] − 1.5  ×  [SO42−], with higher concentrations in December than in November due to lower temperatures. The organic mass fraction was the highest across all PM1 levels throughout the campaign. While organic aerosols (OA were dominated by secondary organic aerosols (SOA  =  semi-volatile oxygenated organic aerosols + low-volatility oxygenated organic aerosols as a campaign average, freshly emitted hydrocarbon-like organic aerosols (HOA contributed up to 40 % of OA during high-OA periods, which typically occurred at nighttime and contributed 23.8 to 28.4 % on average. This was due to daytime traffic restrictions on heavy-duty vehicles in Guangzhou, and HOA almost increased linearly with total OA concentration. SOA increased as odd oxygen (Ox  =  O3 + NO2 increased during the day due to photochemistry. A combination of nighttime traffic emissions and daytime photochemistry contributed to the buildup of PM in Panyu. The mitigation of PM pollution in inner-city areas by reducing vehicular traffic can potentially

  16. 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 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.

  17. Size distributions and formation of ionic species in atmospheric particulate pollutants in Beijing, China: 2—dicarboxylic acids

    Science.gov (United States)

    Yao, Xiaohong; Lau, Arthur P. S.; Fang, Ming; Chan, Chak K.; Hu, Min

    Sparse data on the size distributions of ionic species, especially organic ions, in atmospheric particles are available in the literature. To study the size distributions and the formation of atmospheric ionic species, 14 sets of measurements of the concentrations of the gases and size-segregated atmospheric particles were made in Beijing in the summer of 2001 and the spring of 2002. Significant differences of the size distribution characteristics and the formation mechanism of the ions in these two periods were found. Using the size distributions of SO 42-, K + and Ca 2+ as references, the size distributions of oxalic, malonic and succinic acids were examined to investigate the formation of these acids in the atmospheric particles in Beijing. In the summer, oxalate was present mostly in the fine mode with an MMAD of 0.7±0.1 μm, coincident with the droplet mode of sulfate. The formation of fine mode oxalate, like sulfate, was attributed to in-cloud processes. Malonate was also present mostly in the fine mode with an MMAD of 0.8±0.2 μm and its formation was also attributed to in-cloud processes. The MMAD of fine mode malonate sometimes shifted to values larger than that of sulfate, which can be explained by a minor evaporation of malonate during water evaporation from cloud droplets. The size distribution and the formation of succinate are similar to those of oxalate. In the spring, oxalate sometimes dominated in the fine mode, where oxalate was highly correlated with sulfate ( r=0.86) and had an MMAD (0.45±0.05 μm) similar to sulfate, but it sometimes dominated in the coarse mode, in association with Ca 2+. The fine mode oxalate was attributed to heterogeneous formation but the coarse mode oxalate was probably related to biological formation.

  18. Double Compressions of Atmospheric Depth by Geopotential Tendency, Vorticity, and Atmospheric Boundary Layer Affected Abrupt High Particulate Matter Concentrations at a Coastal City for a Yellow Dust Period in October

    Directory of Open Access Journals (Sweden)

    Hyo Choi

    2014-01-01

    Full Text Available Using GRIMM-aerosol sampler, NOAA-HYSPLIT model, and 3D-WRF-3.3 model, the transportation of dusts from Gobi Desert toward Gangneung city, Korea was investigated from 09:00 LST October 27 to 04:00 LST October 28, 2003. Maximum PM10 (PM2.5, PM1 concentration was detected with 3.8 (3.4, 14.1 times higher magnitude than one in non-Yellow Dust period. The combination of dusts transported from the desert under westerly wind with particulate matters and gases from vehicles on the road of the city caused high PM concentrations near the ground surface at 09:00 LST and their maxima at 17:00 LST near sunset with further pollutants from heating boilers in the resident area. Positive geopotential tendency at the 500 hPa level of the city (∂Φ/∂t; m day−1 corresponding to negative vorticity of -4×10-5 sec−1 (-2.5×10-5 sec−1 at 0900 LST (21:00 LST; at night was +83 m day−1 (+30 m day−1 and it caused atmospheric depth between 500 hPa level and the ground surface to be vertically expanded. However, its net reduction to −53 m/12 hrs until 21:00 LST indicated synoptic-scale atmospheric layer to be vertical shrunken, resulting in the increase of PM concentrations at 17:00 LST. Simultaneously, much shallower microscale stable nocturnal surface inversion layer (NSIL than daytime thermal internal boundary layer induced particulate matters to be merged inside the NSIL, resulting in maximum PM concentrations at 17:00 LST.

  19. The application of carbon-14 analyses to the source apportionment of atmospheric carbonaceous particulate matter: a review.

    Science.gov (United States)

    Heal, Mathew R

    2014-01-01

    Organic carbon (OC) and elemental carbon (EC) together constitute a substantial proportion of airborne particulate matter (PM). Insight into the sources of this major contributor to PM is important for policies to mitigate the impact of PM on human health and climate change. In recent years measurement of the abundance of the radioisotope of carbon ((14)C) in samples of PM by accelerator mass spectrometry has been used to help quantify the relative contributions from sources of fossil carbon and contemporary carbon. This review provides an introduction to the different sources of carbon within PM and the role of (14)C measurements, a description of the preparation of PM samples and of the instrumentation used to quantify (14)C, and a summary of the results and source apportionment methods reported in published studies since 2004. All studies report a sizable fraction of the carbonaceous PM as of non-fossil origin. Even for PM collected in urban locations, the proportions of non-fossil carbon generally exceed 30%; typically the proportion in urban background locations is around 40-60% depending on the local influence of biomass burning. Where values have been measured directly, proportions of non-fossil carbon in EC are lower than in OC, reflecting the greater contribution of fossil-fuel combustion to EC and the generally small sources of contemporary EC. Detailed source apportionment studies point to important contributions from biogenic-derived secondary OC, consistent with other evidence of a ubiquitous presence of heavily oxidized background secondary OC. The review concludes with some comments on current issues and future prospects, including progress towards compound-class and individual-compound-specific (14)C analyses.

  20. In-injection port thermal desorption and subsequent gas chromatography-mass spectrometric analysis of polycyclic aromatic hydrocarbons and n-alkanes in atmospheric aerosol samples.

    Science.gov (United States)

    Ho, Steven Sai Hang; Yu, Jian Zhen

    2004-12-03

    The traditional approach for analysis of aerosol organics is to extract aerosol materials collected on filter substrates with organic solvents followed by solvent evaporation and analytical separation and detection. This approach has the weaknesses of being labor intensive and being prone to contamination from the extracting solvents. We describe here an alternative approach for the analysis of aerosol alkanes and polycyclic aromatic hydrocarbons (PAHs) that obviates the use of solvents. In our approach, small strips of aerosol-laden filter materials are packed into a GC split/splitless injector liner. Alkanes and PAHs on the filter are thermally desorbed in the injection port and focused onto the head of a GC column for subsequent separation and detection. No instrument modification is necessary to accommodate the introduction of the aerosol organics into the GC-MS system. Comparison studies were carried out on a set of 16 ambient aerosol samples using our in-injection port thermal desorption (TD) method and the traditional solvent extraction method. Reasonably good agreement of individual alkanes and PAHs by the two methods was demonstrated for the ambient samples. The in-injection port thermal desorption method requires much less filter material for detecting the same air concentrations of alkanes and PAHs.

  1. Atmospheric Concentrations, Gas/Particle Partitioning And Exposure Risk Of Polycyclic Aromatic Hydrocarbons (PAHs) At Background, Rural Village And Urban Sites In The North China Plain

    Science.gov (United States)

    Wang, W.; Simonich, S.; Zhao, J.; Xue, M.; Wang, W.; Tao, S.

    2009-05-01

    Particle- and gas-phase PAHs were measured in air collected from a background site (Xiaolongmen), two rural village sites (Gubeikou and Donghe), and an urban site (Beijing) located in the North China Plain for four seasons from September 2007 to August 2008 in order to evaluate their concentrations, relative abundance, and gas/particle partitioning. Sixteen PAHs, included in the U.S.EPA priority pollutant list, were determined in the particle (PM10) and gas phases. The annual average 15 PAH concentration in Donghe was 730.7±608.0 ng/m3, which was 18.2, 3.0, 1.8 times higher than Xiaolongmen, Gubeikou and Beijing, respectively. A good linear relationship between gas/particle partitioning coefficients, Kp and subcooled liquid vapor pressure, pl was obtained. At the rural and urban sites, the regression slopes were much steeper than -1, indicating that adsorption of PAH to particulate matter dominated over absorption possibly because, at these sites, the freshly emitted particulate matter and PAHs had not yet reached equilibrium. However, gas/particle partitioning of PAHs approached equilibrium at the background site because of long- range transport of PAHs. In addition, the gas/particle partitioning was studied according to three different models: The Junge-Pankow adsorption model, the Koa absorption model, and the dual organic matter absorption model combined with the soot carbon adsorption model. The Junge-Pankow model and Koa model both under-predicted our experimental Kp values. However, the dual model fit our experimental Kp values well suggesting that the main partitioning mechanism was PAH adsorption onto soot carbon in this region of China. The different particulate matter characteristics (including organic matter and elemental carbon fraction and available adsorption sites), temperature variation during sampling, the presence of a non- exchangeable PAH fraction and non-equilibrium were considered possible reasons for why our experimental Kp values deviated

  2. 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

    Science.gov (United States)

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

    2013-01-01

    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 concentrations were 222 ng/m3 and 114 ng/m3, respectively, with a median total PAH concentration of 349 ng/m3. Higher PAH concentrations were measured in winter than in other seasons. Air PAH concentrations measured at the rural villages and urban sites in the northern mountain region were significantly lower than those measured at sites in the southern plain during all seasons. However, there was no significant difference in PAH concentrations between the rural villages and urban sites in the northern and southern areas. This urban–rural PAH distribution pattern was related to the location of PAH emission sources and the population distribution. The location of PAH emission sources explained 56%–77% of the spatial variation in ambient air PAH concentrations. The annual median air–soil gas exchange flux of PAHs was 42.2 ng/m2/day from soil to air. Among the 15 PAHs measured, acenaphthylene (ACY) and acenaphthene (ACE) contributed to more than half of the total exchange flux. Furthermore, the air–soil gas exchange fluxes of PAHs at the urban sites were higher than those at the remote and rural sites. In summer, more gaseous PAHs volatilized from soil to air because of higher temperatures and increased rainfall. However, in winter, more gaseous PAHs deposited from air to soil due to higher PAH emissions and lower temperatures. The soil TOC concentration had no significant influence on the air–soil gas exchange of PAHs. PMID:21669328

  3. Determination of polycyclic aromatic hydrocarbons in the urine, benzo(a)pyrene diol epoxide-DNA adducts in lymphocyte DNA, and antibodies to the adducts in sera from coke oven workers exposed to measured amounts of polycyclic aromatic hydrocarbons in the work atmosphere.

    Science.gov (United States)

    Haugen, A; Becher, G; Benestad, C; Vahakangas, K; Trivers, G E; Newman, M J; Harris, C C

    1986-08-01

    Workers in coke oven plants have a higher incidence of lung cancer than the general population. They are exposed to a variety of chemicals, in particular the polycyclic aromatic hydrocarbons (PAH), including benzo(a)pyrene. To evaluate the genotoxic effects of PAH exposure, air samples and urine samples were analyzed for PAH by capillary gas chromatography and high-performance liquid chromatography, respectively. Since benzo(a)pyrene is activated to 7 beta,8 alpha-dihydroxy-(9 alpha,10 alpha)-epoxy-7,8,9,10-tetrahydrobenzo(a)pyrene (BPDE) and binds to DNA, we have used ultrasensitive enzymatic radioimmunoassay and synchronous fluorescence spectrophotometry to measure BPDE-DNA adducts in lymphocyte DNA. The results show that workers were exposed to high concentrations of atmospheric PAH. However, the mean PAH exposure levels are reduced 60% when the workers wore masks during work. When compared to exposure levels, the urinary excretion of PAH was relatively low. Approximately one-third of the workers had detectable putative BPDE-DNA adducts in lymphocytes by ultrasensitive enzymatic radioimmunoassay, and 10% of the samples had emission peaks at 379 nm by synchronous fluorescence spectrophotometry. The four most positive samples were the same in both of the assays. Antibodies to an epitope(s) on BPDE-DNA were found in the sera of approximately one-third of the workers. Detection of DNA adducts and antibodies to these adducts are internal indicators of exposure to benzo(a)pyrene.

  4. Contributions of nitrated aromatic compounds to the light absorption of water-soluble and particulate brown carbon in different atmospheric environments

    Science.gov (United States)

    Teich, Monique; van Pinxteren, Dominik; Wang, Michael; Kecorius, Simonas; Wang, Zhibin; Müller, Thomas; Močnik, Griša; Herrmann, Hartmut

    2017-04-01

    Recently the importance of light absorbing carbon, so-called brown carbon (BrC), on aerosol light absorption properties became more and more evident. The presence of BrC can enhance the light absorption of aerosols and therefore have an impact on the earth climate system. Despite the numerous studies published in the past few years little is known about the molecular composition and sources of BrC or the impact of single organic molecules on the BrC light absorption. The present study aims to deepen the understanding of atmospheric particulate and water soluble BrC by determining the ambient concentrations of eight individual nitrated aromatic compounds (nitrophenols and nitrated salicylic acids), and connecting the obtained chemical information with the light absorption properties of aqueous particle extracts (indicating water soluble BrC) and the overall particulate BrC light absorption. High-volume filter samples were collected during six campaigns, performed at five locations in two seasons: (I) two campaigns with strong influence of biomass burning (BB) aerosol - at the TROPOS institute (winter, 2014, urban background, Leipzig, Germany) and the Melpitz research site (winter, 2014, rural background); (II) two campaigns with strong influence from biogenic emissions - at Melpitz (summer, 2014) and the forest site Waldstein (summer, 2014, Fichtelgebirge, Germany), and (III) two CAREBeijing-NCP campaigns - at Xianghe (summer, 2013, anthropogenic polluted background) and Wangdu (summer, 2014, anthropogenic polluted background with a distinct BB-episode), both in the North China Plain. The light absorption properties of the aqueous particle extracts were determined by UV/Vis spectrometry for the same set of filter samples. Particulate BrC light absorption properties were derived from a seven-wavelength Aethalometer for a subset of these samples. A clear seasonality was observed in the data from the German sites where higher concentrations as well as higher light

  5. Retrieval of High-Resolution Atmospheric Particulate Matter Concentrations from Satellite-Based Aerosol Optical Thickness over the Pearl River Delta Area, China

    Directory of Open Access Journals (Sweden)

    Lili Li

    2015-06-01

    Full Text Available Satellite remote sensing offers an effective approach to estimate indicators of air quality on a large scale. It is critically significant for air quality monitoring in areas experiencing rapid urbanization and consequently severe air pollution, like the Pearl River Delta (PRD in China. This paper starts with examining ground observations of particulate matter (PM and the relationship between PM10 (particles smaller than 10 μm and aerosol optical thickness (AOT by analyzing observations on the sampling sites in the PRD. A linear regression (R2 = 0.51 is carried out using MODIS-derived 500 m-resolution AOT and PM10 concentration from monitoring stations. Data of atmospheric boundary layer (ABL height and relative humidity are used to make vertical and humidity corrections on AOT. Results after correction show higher correlations (R2 = 0.55 between extinction coefficient and PM10. However, coarse spatial resolution of meteorological data affects the smoothness of retrieved maps, which suggests high-resolution and accurate meteorological data are critical to increase retrieval accuracy of PM. Finally, the model provides the spatial distribution maps of instantaneous and yearly average PM10 over the PRD. It is proved that observed PM10 is more relevant to yearly mean AOT than instantaneous values.

  6. 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.

    Science.gov (United States)

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

    2011-07-01

    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 concentrations were 222 ng/m³ and 114 ng/m³, respectively, with a median total PAH concentration of 349 ng/m³. Higher PAH concentrations were measured in winter than in other seasons. Air PAH concentrations measured at the rural villages and urban sites in the northern mountain region were significantly lower than those measured at sites in the southern plain during all seasons. However, there was no significant difference in PAH concentrations between the rural villages and urban sites in the northern and southern areas. This urban-rural PAH distribution pattern was related to the location of PAH emission sources and the population distribution. The location of PAH emission sources explained 56%-77% of the spatial variation in ambient air PAH concentrations. The annual median air-soil gas exchange flux of PAHs was 42.2 ng/m²/day from soil to air. Among the 15 PAHs measured, acenaphthylene (ACY) and acenaphthene (ACE) contributed to more than half of the total exchange flux. Furthermore, the air-soil gas exchange fluxes of PAHs at the urban sites were higher than those at the remote and rural sites. In summer, more gaseous PAHs volatilized from soil to air because of higher temperatures and increased rainfall. However, in winter, more gaseous PAHs deposited from air to soil due to higher PAH emissions and lower temperatures. The soil TOC concentration had no significant influence on the air-soil gas exchange of PAHs. Copyright © 2011 Elsevier B.V. All rights reserved.

  7. 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

  8. Atmospheric Corrections and Multi-Conditional Algorithm for Multi-Sensor Remote Sensing of Suspended Particulate Matter in Low-to-High Turbidity Levels Coastal Waters

    Directory of Open Access Journals (Sweden)

    Stéfani Novoa

    2017-01-01

    Full Text Available The accurate measurement of suspended particulate matter (SPM concentrations in coastal waters is of crucial importance for ecosystem studies, sediment transport monitoring, and assessment of anthropogenic impacts in the coastal ocean. Ocean color remote sensing is an efficient tool to monitor SPM spatio-temporal variability in coastal waters. However, near-shore satellite images are complex to correct for atmospheric effects due to the proximity of land and to the high level of reflectance caused by high SPM concentrations in the visible and near-infrared spectral regions. The water reflectance signal (ρw tends to saturate at short visible wavelengths when the SPM concentration increases. Using a comprehensive dataset of high-resolution satellite imagery and in situ SPM and water reflectance data, this study presents (i an assessment of existing atmospheric correction (AC algorithms developed for turbid coastal waters; and (ii a switching method that automatically selects the most sensitive SPM vs. ρw relationship, to avoid saturation effects when computing the SPM concentration. The approach is applied to satellite data acquired by three medium-high spatial resolution sensors (Landsat-8/Operational Land Imager, National Polar-Orbiting Partnership/Visible Infrared Imaging Radiometer Suite and Aqua/Moderate Resolution Imaging Spectrometer to map the SPM concentration in some of the most turbid areas of the European coastal ocean, namely the Gironde and Loire estuaries as well as Bourgneuf Bay on the French Atlantic coast. For all three sensors, AC methods based on the use of short-wave infrared (SWIR spectral bands were tested, and the consistency of the retrieved water reflectance was examined along transects from low- to high-turbidity waters. For OLI data, we also compared a SWIR-based AC (ACOLITE with a method based on multi-temporal analyses of atmospheric constituents (MACCS. For the selected scenes, the ACOLITE-MACCS difference was

  9. Polycyclic musk fragrances in the aquatic environment.

    Science.gov (United States)

    Rimkus, G G

    1999-12-20

    The polycyclic musk fragrances, mainly 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-ben zopyrane (HHCB) and 7-acetyl-1,1,3,4,4,6-hexamethyltetrahydronaphthalene (AHTN) are synthetic musk fragrances which are used in almost all scented consumer products, such as perfumes, cosmetics and laundry detergents. Concerning their chemical structures the polycyclic musks are indane and tetraline derivatives highly substituted mainly by methyl groups. Their production has been increased continuously during the last years with a world-wide production volume today of about 6000 t/year. After their application in private households they are dumped via the sewage treatment plants into the aquatic environment. In this review the analysis of polycyclic musk compounds in environmental samples is shortly presented and all published data of polycyclic musk compounds in water, sediment, suspended particulate matter (SPM), sewage sludge, and biota are summarized and discussed. The highest HHCB and AHTN concentrations were analysed in water (maximum concentrations: 6 microg HHCB/l, 4.4 microg AHTN/1) and sludge (maximum concentrations: 63 mg HHCB/kg dry matter, 34 mg AHTN/kg dry matter) from sewage plants, and in fish (maximum concentrations: 159 mg HHCB/kg lipid, 58 mg AHTN/kg lipid) from sewage ponds. In all other samples from different aquatic ecosystems these chemicals were unequivocally detected in varying concentrations dependent on the distance to sewage treatment plants. Even in marine water samples from the German Bight HHCB and AHTN could be quantified at the lower ng/l level. Very often HHCB and AHTN formed the major organic contaminants, in all samples their concentrations exceeded those of musk xylene and musk ketone. Also several by-products and impurities of the commercial polycyclic musks were analysed in river and waste water samples in not negligible amounts. The apparently ubiquitous distribution of polycyclic musks in the aquatic environment

  10. Atmospheric pollution in Lisbon urban atmosphere

    Science.gov (United States)

    Oliveira, C.

    2009-04-01

    Lisbon is the capital city of Portugal with about 565,000 residents in 2008 and a population density of 6,600 inhabitants per square kilometre. Like several other major metropolis, the town is surrounded by satellite cities, forming together a region known as "Lisbon Metropolitan Area" with about 3 million inhabitants, a quarter of the overall Portuguese population. Besides their local residents, it is estimated that more than one million citizens come into the Lisbon area every day from the outskirts, leading to elevated traffic densities and intense traffic jams, with important consequences on air pollution levels and obvious negative impacts on human health. Airborne particulate matter limit values are frequently exceeded, making urgent the existence of consistent programs to monitor and help taking measures to control them. Within the Portuguese project PAHLIS (Polycyclic Aromatic Hydrocarbons Contamination in Lisbon Urban Atmosphere) financed by the Portuguese Science Foundation ("Fundação para a Ciência e a Tecnologia"), an aerosol and vapour phase sampling program is being implemented in the city of Lisbon at two selected contrasting zones, namely a typically busy area with intense road traffic and frequent exceedences of the particulate matter standard for the maximum allowable concentration, and a residential quieter area, thus with a cleaner atmosphere characterised as an urban background site. An one month-long sampling campaign was performed during the summer of 2008, where particulate matter was collected in two fractions (coarse 2.5µmcommunication, the results of both organic and inorganic analyses of aerosol samples from these two sites will be presented, compared and discussed. Results of this work are expected to cover a lack of reliable information regarding sources of atmospheric pollutants in Portugal and present, for the first time, systematic data of PAHs levels in Lisbon. Acknowledgement: This work was performed under Project PAHLIS (PTDC

  11. Regional modelling of polycyclic aromatic hydrocarbons: WRF-Chem-PAH model development and East Asia case studies

    Directory of Open Access Journals (Sweden)

    Q. Mu

    2017-10-01

    Full Text Available Polycyclic aromatic hydrocarbons (PAHs are hazardous pollutants, with increasing emissions in pace with economic development in East Asia, but their distribution and fate in the atmosphere are not yet well understood. We extended the regional atmospheric chemistry model WRF-Chem (Weather Research Forecast model with Chemistry module to comprehensively study the atmospheric distribution and the fate of low-concentration, slowly degrading semivolatile compounds. The WRF-Chem-PAH model reflects the state-of-the-art understanding of current PAHs studies with several new or updated features. It was applied for PAHs covering a wide range of volatility and hydrophobicity, i.e. phenanthrene, chrysene and benzo[a]pyrene, in East Asia. Temporally highly resolved PAH concentrations and particulate mass fractions were evaluated against observations. The WRF-Chem-PAH model is able to reasonably well simulate the concentration levels and particulate mass fractions of PAHs near the sources and at a remote outflow region of East Asia, in high spatial and temporal resolutions. Sensitivity study shows that the heterogeneous reaction with ozone and the homogeneous reaction with the nitrate radical significantly influence the fate and distributions of PAHs. The methods to implement new species and to correct the transport problems can be applied to other newly implemented species in WRF-Chem.

  12. Regional modelling of polycyclic aromatic hydrocarbons: WRF-Chem-PAH model development and East Asia case studies

    Science.gov (United States)

    Mu, Qing; Lammel, Gerhard; Gencarelli, Christian N.; Hedgecock, Ian M.; Chen, Ying; Přibylová, Petra; Teich, Monique; Zhang, Yuxuan; Zheng, Guangjie; van Pinxteren, Dominik; Zhang, Qiang; Herrmann, Hartmut; Shiraiwa, Manabu; Spichtinger, Peter; Su, Hang; Pöschl, Ulrich; Cheng, Yafang

    2017-10-01

    Polycyclic aromatic hydrocarbons (PAHs) are hazardous pollutants, with increasing emissions in pace with economic development in East Asia, but their distribution and fate in the atmosphere are not yet well understood. We extended the regional atmospheric chemistry model WRF-Chem (Weather Research Forecast model with Chemistry module) to comprehensively study the atmospheric distribution and the fate of low-concentration, slowly degrading semivolatile compounds. The WRF-Chem-PAH model reflects the state-of-the-art understanding of current PAHs studies with several new or updated features. It was applied for PAHs covering a wide range of volatility and hydrophobicity, i.e. phenanthrene, chrysene and benzo[a]pyrene, in East Asia. Temporally highly resolved PAH concentrations and particulate mass fractions were evaluated against observations. The WRF-Chem-PAH model is able to reasonably well simulate the concentration levels and particulate mass fractions of PAHs near the sources and at a remote outflow region of East Asia, in high spatial and temporal resolutions. Sensitivity study shows that the heterogeneous reaction with ozone and the homogeneous reaction with the nitrate radical significantly influence the fate and distributions of PAHs. The methods to implement new species and to correct the transport problems can be applied to other newly implemented species in WRF-Chem.

  13. Exposure to polycyclic aromatic hydrocarbons in atmospheric PM1.0 of urban environments: Carcinogenic and mutagenic respiratory health risk by age groups.

    Science.gov (United States)

    Agudelo-Castañeda, Dayana M; Teixeira, Elba C; Schneider, Ismael L; Lara, Sheila Rincón; Silva, Luis F O

    2017-05-01

    We investigated the carcinogenic and mutagenic respiratory health risks related to the exposure to atmospheric PAHs in an urban area. Our study focused in the association of these pollutants and their possible effect in human health, principally respiratory and circulatory diseases. Also, we determined a relationship between the inhalation risk of PAHs and meteorological conditions. We validated the hypothesis that in winter PAHs with high molecular weight associated to submicron particles (PM1) may increase exposure risk, especially for respiratory diseases, bronchitis and pneumonia diseases. Moreover, in our study we verified the relationship between diseases and several carcinogenic PAHs (Ind, BbkF, DahA, BaP, and BghiP). These individual PAHs contributed the most to the potential risk of exposure for inhalation of PM1.0. Even at lower ambient concentrations of BaP and DahA in comparison with individual concentrations of other PAHs associated to PM1.0. Mainly, research suggests to include carcinogenic and mutagenic PAHs in future studies of environmental health risk due to their capacity to associate to PM10. Such carcinogenic and mutagenic PAHs are likely to provide the majority of the human exposure, since they originate from dense traffic urban areas were humans congregate. Copyright © 2017 Elsevier Ltd. All rights reserved.

  14. 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

  15. SHORT COMMUNICATION POLYCYCLIC AROMATIC ...

    African Journals Online (AJOL)

    a

    ______. *Corresponding author. E-mail: omotayosharafdeen@yahoo.com. SHORT COMMUNICATION. POLYCYCLIC AROMATIC HYDROCARBONS IN MUNICIPAL WASTE ASHES. FROM THREE WASTE DUMPS IN LAGOS, NIGERIA. O.S. Amuda* and F.E. Adelowo-Imeokparia. Environmental/Analytical Chemistry Unit, ...

  16. 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

  17. Fluorescence spectrophotometer analysis of polycyclic aromatic hydrocarbons in environmental samples based on solid phase extraction using molecularly imprinted polymer.

    Science.gov (United States)

    Krupadam, Reddithota J; Bhagat, Bhagyashree; Wate, Satish R; Bodhe, Ghanshyam L; Sellergren, Borje; Anjaneyulu, Yerramilli

    2009-04-15

    A molecularly imprinted polymer (MIP) was synthesized using a polycyclic aromatic hydrocarbon (PAH) standard as a template, methacrylic acid as a functional monomer, ethylene glycol dimethacrylate as a cross-linker, and acetonitrile as a porogen. This polymer was used as a solid phase adsorbent for the quantitative enrichment of PAHs in coastal sediments, atmospheric particulates, and industrial effluents. The MIP selective adsorption capacity for PAHs started reducing when the chemical oxygen demand (COD) and total dissolved solids (TDS) was more than 800 mg L(-1) in the targeted environmental samples. The adsorption stability of the MIP was tested by the consecutive contact of environmental samples, and it was shown that the performance of the MIP did not vary after 10 enrichments and desorption cycles. Recoveries of eight PAH compounds, extracted from 10 g of coastal sediments and 1 L of industrial effluent spiked with 10 microL of standard PAHs, showed recoveries between 85 and 96%. The fluorescence spectrophotometer limit of detection of PAHs varied from 10 to 30 etag L(-1) in industrial effluent and from 0.1 to 2.9 etag kg(-1) in solid samples (coastal sediment and atmospheric particulates), and this indicates that the environmental analytical method is significantly sensitive, when compared with other commonly used methods such as gas chromatography-mass spectrometry and liquid chromatography-mass spectrometry.

  18. 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)

  19. Source apportionment of atmospheric particulate matter (PM) using a constrained US-EPA-PMF5.0 model at different urban environments in France

    Science.gov (United States)

    Salameh, Dalia; Favez, Olivier; Golly, Benjamin; Besombes, Jean Luc; Alleman, Laurent; Albinet, Alexandre; Jaffrezo, Jean Luc

    2017-04-01

    Particulate matter (PM) is one of the most studied atmospheric pollutant in urban areas due to their adverse effects on human health (Pope et al., 2009). Intrinsic properties of PM (e.g. chemical composition and morphology) are directly linked to their origins. Therefore, a harmonized and comprehensive apportionment study of PM sources in urban environments is extremely required to connect source contributions with PM concentration levels and then develop effective PM abatement strategies. Multivariate receptor models such as Positive Matrix Factorization (PMF) are very useful and have been used worldwide for PM source apportionment (Viana et al., 2008). PMF uses a weighted least-squares fit and quantitatively determines source fingerprints (factors) and their contributions to the total PM mass. However, in many cases, it could be tricky to separate two factors that co-vary due to similar seasonal variations, making unclear the physical sense of the extracted factors. To address such issues of source collinearities, additional specific constraints are incorporated into the model (i.e., constrained PMF) based on user's external knowledge allowing better apportionment results. In this work and within the framework of the SOURCES project, a harmonized source apportionment approach has been implemented and applied for the determination of PM sources on a large number of sites (up to 20) of different typologies (e.g. urban background, industrial, traffic, rural and/or alpine sites) distributed all over France and previously investigated with annual or multiannual studies (2012-2016). A constrained PMF approach (using US-EPA PMF5.0 software) was applied to the comprehensive PM-offline chemical datasets (i.e. carbonaceous fraction, major ions, metals/trace elements, specific organic markers) in a harmonized way for all the investigated sites. Different types of specific chemical constraints from well-characterized sources were defined based on external knowledge and were

  20. Polycyclic aromatic hydrocarbons in freshwater isopods and field-partitioning between abiotic phases

    NARCIS (Netherlands)

    van Hattum, A.G.M.; Curto Pons, M.J.; Cid Montañés, J.F.

    1998-01-01

    An assessment was made of the in situ bioaccumulation of 13 polycyclic aromatic hydrocarbons (PAHs) in freshwater isopods in relation to their partitioning between sediments, particulate matter (>0.7 μm), and dissolved phases in eight different water systems of The Netherlands. Large differences in

  1. Source apportionment of polycyclic aromatic hydrocarbon in soil ...

    African Journals Online (AJOL)

    The13C/12C isotopic ratios of polycyclic aromatic hydrocarbons (PHCs) for soil samples collected and preserved from contact with any other source(s) of PAHs except atmospheric, between the years 1865 and 1986 in the United Kingdom, were determined, in order to understand PAHs source apportionment within the ...

  2. Retrieval of High-Resolution Atmospheric Particulate Matter Concentrations from Satellite-Based Aerosol Optical Thickness over the Pearl River Delta Area, China

    OpenAIRE

    Lili Li; Jingxue Yang; Yunpeng Wang

    2015-01-01

    Satellite remote sensing offers an effective approach to estimate indicators of air quality on a large scale. It is critically significant for air quality monitoring in areas experiencing rapid urbanization and consequently severe air pollution, like the Pearl River Delta (PRD) in China. This paper starts with examining ground observations of particulate matter (PM) and the relationship between PM10 (particles smaller than 10 μm) and aerosol optical thickness (AOT) by analyzing observations o...

  3. 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.

  4. Lung antioxidant and cytokine responses to coarse and fine particulate matter from the great California wildfires of 2008.

    Science.gov (United States)

    Wegesser, Teresa C; Franzi, Lisa M; Mitloehner, Frank M; Eiguren-Fernandez, Arantza; Last, Jerold A

    2010-06-01

    The authors have previously demonstrated that wildfire-derived coarse or fine particulate matter (PM) intratracheally instilled into lungs of mice induce a strong inflammatory response. In the current study, the authors demonstrate that wildfire PM simultaneously cause major increases in oxidative stress in the mouse lungs as measured by decreased antioxidant content of the lung lavage supernatant fluid 6 and 24 h after PM administration. Concentrations of neutrophil chemokines/cytokines and of tumor necrosis factor (TNF)-alpha were elevated in the lung lavage fluid obtained 6 and 24 h after PM instillation, consistent with the strong neutrophilic inflammatory response observed in the lungs 24 h after PM administration, suggesting a relationship between the proinflammatory activity of the PM and the measured level of antioxidant capacity in the lung lavage fluid. Chemical analysis shows relatively low levels of polycyclic aromatic hydrocarbons compared to published results from typical urban PM. Coarse PM fraction is more active (proinflammatory activity and oxidative stress) on an equal-dose basis than the fine PM despite its lower content of polycyclic aromatic hydrocarbons. There does not seem to be any correlation between the content of any specific polycyclic aromatic hydrocarbon (or of total polycyclic aromatic hydrocarbon content) in the PM fraction and its toxicity. However, the concentrations of the oxidation products of phenanthrene and anthracene, phenanthraquinone and anthraquinone, were several-fold higher in the coarse PM than the fine fraction, suggesting a significant role for atmospheric photochemistry in the formation of secondary pollutants in the wildfire PM and the possibility that such secondary pollutants could be significant sources of toxicity in the wildfire PM.

  5. Polycyclic aromatic hydrocarbons and their nitrated derivatives associated with PM10 from Kraków city during heating season

    Directory of Open Access Journals (Sweden)

    Styszko Katarzyna

    2016-01-01

    Full Text Available Polycyclic Aromatic Hydrocarbons (PAHs, their nitro-derivatives (NPAHs and hundreds of other organic compounds are present in ambient air in gas and particulate form. PAHs and NPAHs originate from diesel and gasoline exhaust emission and other combustion sources. NPAHs are also formed through the nitration of parent PAHs in the atmosphere. Concentrations of PAHs and NPAHs in the particulate matter fraction PM10 collected in the centre of Kraków (27.01.2014 – 17.02.2014 were investigated. The thirteen PAHs and four NPAHs: fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benzo[a]anthracene, benzo[a]pyrene, chrysene, benzo[b]fluoranthene, benzo[k]fluoranthene, indeno[1,2,3-c,d]pyrene, benzo[g,h,i]perylene, dibenz[a,h]anthracene, 2-nitrofluorene, 9-nitroanthracene, 3-nitrofluoranthene and 1-nitropyrene were extracted from particulate matter and analysed applying the GC/MS technique. Depending on the compounds the relative recoveries ranged from 72 to 94%. The concentrations of PM10 in the study period ranged between 23.5 and 153.8 μg·m-3. The average concentrations of PAHs and NPAHs ranged from 26.6 to 276.4 ng·m-3 and from 0.6 to 9.1 ng·m-3, respectively. The highest concentrations were observed for benzo[a]pyrene, benzo[a]anthracene, pyrene and fluoranthene. The average concentration of benzo[a]pyrene (BaP, which is a marker for the particle-bound atmospheric PAHs, was 9.5 ng·m-3. The concentrations of 3-nitrofluoranthene and 1-nitropyrene were below the quantification limits of the method (< MQL.

  6. 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 of...

  7. 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 (0...

  8. Urinary metabolites of polycyclic aromatic hydrocarbons in Saudi Arabian schoolchildren in relation to sources of exposure.

    Science.gov (United States)

    Alghamdi, Mansour A; Alam, Mohammed S; Stark, Christopher; Mohammed, Nuredin; Harrison, Roy M; Shamy, Magdy; Khoder, Mamdouh I; Shabbaj, Ibrahim I; Göen, Thomas

    2015-07-01

    Polycyclic aromatic hydrocarbons contain a number of known carcinogenic compounds, and urinary biomarkers have been widely used as a measure of exposure but quantitative relationships with exposure variables have proved elusive. This study aimed to quantify the relationship between exposures to phenanthrene and pyrene from atmospheric and dietary sources with the excretion of 1-hydroxypyrene and hydroxyphenanthrenes in urine as biomarkers of exposure. The study population consisted of 204 male schoolchildren attending three schools in different parts of Jeddah, Saudi Arabia who provided urine samples on each of three consecutive days. Outdoor air measurements of polycyclic aromatic hydrocarbons were made at the schools and the children provided information on diet, exposure to environmental tobacco smoke and incense, and various lifestyle factors through a questionnaire. Mixed models with random effects for subjects nested within site were fitted in order to examine the relationship between exposure variables and urinary PAH metabolites. A unit increase (1 ng m(-3)) in ambient pyrene (particulate plus gaseous phase) was associated with a 3.5% (95% CI: 1.01%, 5.13%) increase in urinary 1-hydroxypyrene concentration. A unit increase in ambient phenanthrene was associated with a 1.01% (95% CI: 0.03%, 2.02%) increase in total hydroxyphenanthrene concentrations. Consumption of chargrilled food increased the 1-hydroxypyrene and hydroxyphenanthrene concentrations by 24% (95% CI: 11%, 37%) and 17% (95% CI: 8%, 26%) respectively. We did not find evidence of association for environmental tobacco smoke exposure or incense burning. It is concluded that both respiratory exposure and consumption of chargrilled food are considerable sources of PAH exposure in this population as reflected by concentrations of urinary biomarkers. Copyright © 2015 Elsevier Inc. All rights reserved.

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

    Science.gov (United States)

    Sun, Li; Zang, Shuying

    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 (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. Copyright © 2013 Elsevier B.V. All rights reserved.

  10. EPR investigations of Mn{sup 2+}, Fe{sup 3+} ions and carbonaceous radicals in atmospheric particulate aerosols during their transport over the eastern coast of the English Channel

    Energy Technology Data Exchange (ETDEWEB)

    Ledoux, F.; Bouhsina, S.; Courcot, L.; Bertho, M.L.; Puskaric, E. [Universite du Littoral Cote d' Opale, Wimereaux (France). Lab. Interdisciplinaire en Sciences de l' Environnement; Zhilinskaya, E.; Aboukais, A. [Universite du Littoral Cote d' Opale, Wimereaux (France). Lab. de Catalyse et Environnement

    2002-07-01

    Electron paramagnetic resonance (EPR) spectroscopy was used to follow the evolution of the chemical forms of manganese and study other paramagnetic species in the atmospheric particulate aerosols at Wimereux, a French station located on the eastern coast of the English Channel. In parallel, Graphite Furnace Atomic Absorption Spectrometry (GFAAS) was used to measure the metal concentrations. Fe concentration values are common in North Sea sites, but those of Mn are quite higher due to the presence of an important local source of Mn. EPR spectra have evidenced isolated Fe{sup 3+} and Mn{sup 2+} ions and carbonaceous products with variable intensities according to the wind directions. Amounts of paramagnetic species and carbonaceous products are maximum for continental winds and minimum for marine winds. Three Mn types were identified depending on the sampling distance from the source of emission and the size of the particles. (Author)

  11. Assessing atmospheric particulate matter distribution based on Saturation Isothermal Remanent Magnetization of herbaceous and tree leaves in a tropical urban environment.

    Science.gov (United States)

    Barima, Yao Sadaiou Sabas; Angaman, Djédoux Maxime; N'gouran, Kobenan Pierre; Koffi, N'guessan Achille; Kardel, Fatemeh; De Cannière, Charles; Samson, Roeland

    2014-02-01

    Particulate matter (PM) emissions, and the associated human health risks, are likely to continue increasing in urban environments of developing countries like Abidjan (Ivory Cost). This study evaluated the potential of leaves of several herbaceous and tree species as bioindicators of urban particulate matter pollution, and its variation over different land use classes, in a tropical area. Four species well distributed (presence frequencies >90%) over all land use classes, easy to harvest and whose leaves are wide enough to be easily scanned were selected, i.e.: Amaranthus spinosus (Amaranthaceae), Eleusine indica (Poaceae), Panicum maximum (Poaceae) and Ficus benjamina (Moraceae). Leaf sampling of these species was carried out at 3 distances from the road and at 3 height levels. Traffic density was also noted and finally biomagnetic parameters of these leaves were determined. Results showed that Saturation Isothermal Remanent Magnetization (SIRM) of leaves was at least 4 times higher (27.5×10(-6)A) in the vicinity of main roads and industrial areas than in parks and residential areas. The main potential sources of PM pollution were motor vehicles and industries. The slightly hairy leaves of the herbaceous plant A. spinosus and the waxy leaves of the tree F. benjamina showed the highest SIRM (25×10(-6)A). Leaf SIRM increased with distance to road (R(2)>0.40) and declined with sampling height (R(2)=0.17). The distance between 0 and 5m from the road seemed to be the most vulnerable in terms of PM pollution. This study has showed that leaf SIRM of herbaceous and tree species can be used to assess PM exposure in tropical urban environments. © 2013.

  12. DETERMINATION OF POLYCYCLIC AROMATIC HYDROCARBONS ...

    African Journals Online (AJOL)

    AMOS

    Scomber scombrus), suya beef and plantain (Musa paradiasca) sold and consumed in Amassoma town were screened for the presence of 15 polycyclic aromatic hydrocarbons (PAHs). Concentration of chromium, lead and cadmium were also ...

  13. 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.

  14. Atmospheric particulate deposition in temperate deciduous forest ecosystems: interactions with the canopy and nutrient inputs in two beech stands of Northeastern France.

    Science.gov (United States)

    Lequy, Emeline; Calvaruso, Christophe; Conil, Sébastien; Turpault, Marie-Pierre

    2014-07-15

    As wood harvests are expected to increase to satisfy the need for bio-energy in Europe, quantifying atmospheric nutrient inputs in forest ecosystems is essential for forest management. Current atmospheric measurements only take into account the 0.45 μm fraction of atmospheric deposition, below the canopy, to study the influence of the canopy on APD, and to determine the influence of APD below canopy to nutrient input-output budgets with a focus on base cations calcium, magnesium and potassium, and phosphorus. APD was sampled every four weeks by passive collectors. We divided APD into an organic and a mineral fraction, respectively POM and MDD. MDD was divided into a soluble and a hardly soluble fraction in hydrogen peroxide, referred to as S-MDD and H-MDD, respectively. In order to better understand the influence of the canopy on APD, we studied APD in three pathways below the canopy (litterfall, stemflow and throughfall), and in open field. Our results indicated that APD in throughfall (123 ± 64 kg ha(-1)year(-1)) was significantly higher and synchronic with that in open field (33 ±9 kg ha(-1)year(-1)) in the two study sites. This concerned both POM and MDD, suggesting a large interception of APD by foliar surfaces, which is rapidly washed off by rain within four weeks. Throughfall H-MDD was the main pathway with an average of 16 ± 2 kg ha(-1)year(-1). Stemflow and litterfall were neglected. In one study site, canopy intercepted about 8 kg ha(-1)year(-1) of S-MDD. Although base cations and phosphorus inputs by APD are lower than those of <0.45 μm deposition, they contributed from 5 to 32% to atmospheric deposition and improved the nutrient budget in one of the study sites. Copyright © 2014 Elsevier B.V. All rights reserved.

  15. 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...

  16. Seasonal progression of atmospheric particulate matter over an urban coastal region in peninsular India: Role of local meteorology and long-range transport

    Science.gov (United States)

    Mahapatra, P. S.; Sinha, P. R.; Boopathy, R.; Das, T.; Mohanty, S.; Sahu, S. C.; Gurjar, B. R.

    2018-01-01

    Measurement of particulate matter (PM) over an urban site with relatively high concentration of aerosol particles is critically important owing to its adverse health, environmental and climate impact. Here we present a 3 years' worth of measurements (January 2012 to December 2014) of PM2.5 (aerodynamic diameter of less than 2.5 μm) and PM10 (aerodynamic diameter of less than 10 μm) along with meteorological parameters and seasonal variations at Bhubaneswar an urban-coastal site, in eastern India. The concentrations of PM were determined gravimetrically from the filter samples of PM2.5 and PM10. It revealed remarkable seasonal variations with winter values (55.0 ± 23.4 μg/m3; 147.3 ± 42.4 μg/m3 for PM2.5 and PM10, respectively) about 3.5 times higher than that in pre-monsoon (15.7 ± 6.2 μg/m3; 41.8 ± 15.3 μg/m3). PM2.5 and PM10 were well correlated while PM2.5/PM10 ratios were found to be 0.38 and 0.32 during winter and pre-monsoon, indicating the predominance of coarse particles, mainly originating from long range transport of pollutants from northern and western parts of India and parts of west Asia as well. Concentration weighted trajectory (CWT) analysis revealed the IGP and North Western Odisha as the most potential sources of PM2.5 and PM10 during winter. The PM concentrations at Bhubaneswar were comparable with those at other coastal sites of India reported in the literature, but were lower than few polluted urban sites in India and Asia. Empirical model reproduced the observed seasonal variation of PM2.5 and PM10 very well over Bhubaneswar.

  17. Determination of barium, chromium, cadmium, manganese, lead and zinc in atmospheric particulate matter by inductively coupled plasma atomic emission spectrometry (ICP-AES)

    Science.gov (United States)

    Boevski, I. V.; Daskalova, N.; Havezov, I.

    2000-11-01

    The present paper has shown that the Q concept, as proposed by P.W.J.M. Boumans, J.J.A.M. Vrakking, Spectrochim. Acta Part B 43 (1988) 69, can be used as a basic methodology in the determination of Ba, Cr, Cd, Mn, Pb and Zn in pairs of atmospheric particles by inductively coupled plasma atomic emission spectrometry (ICP-AES). The data base of Q values for line interference [ QIj(λ a)] and Q values for wing background interference [ QWJ(Δλ a)] were obtained in our former work [N. Daskalova, Iv. Boevski, Spectral interferences in the determination of trace elements in environmental materials by inductively coupled plasma atomic emission spectrometry, Spectrochim. Acta Part B 54 (1999) 1099-1122]. The samples of atmospheric particles were collected by the Bergerhoff method. The ICP-AES determination was performed after sample digestion with aqua regia. Q values were used for the calculation of both the total interfering signal under the analysis lines and the true detection limits, depending on the matrix constituents in the different samples. Comparative data for the concentration of analytes were obtained by flame atomic absorption spectrometry (FAAS) and direct current arc atomic emission spectrographic method (dc arc-AES).

  18. 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.

  19. Assessment of social losses of pollution's health caused by man-made pollution of atmospheric air with emissions of particulate matters (PM10

    Directory of Open Access Journals (Sweden)

    Turos Ye.I.

    2017-04-01

    Full Text Available According to available estimates, about 3% of lethal outcomes from cardiac-pulmonary pathology and 5% from lung cancer are related to the impact of patriculate matters (PM. In the course of the study there were assessed social losses of population’s health (additional death cases caused by risk conditions of atmospheric air pollution with PM of various air-dynamic diameter (PM10, proper to emissions of various industrial enterprises. It was established that 90% of population of cities under study live under high exposures (≥50 µg/m3 health and risks for population (IRM=10-3÷10-4, caused by PM10 emissions. Results showed that metallurgical industry is responsible for 7,2 to 2193 additional mortality cases. The impact of machine building enterprises – from 0.06 to 21 cases; coke and chemical – from 1.5 to 36 cases; mining – from 1.1 to 14,6 cases. The findings revealed 0.6 % increase in lifetime mortality for each 10 µg/m3 in 24-hour average PM10 concentration. Based on research outcomes, a set of instruments was developed for implementation of air pollution risk management programs aimed at mitigation of health risks from (PM10 in highly exposed groups.

  20. Assessment of exposure to atmospheric particles: contribution of individual measurements; Evaluation de l'exposition aux particules atmospheriques: apport des mesures individuelles

    Energy Technology Data Exchange (ETDEWEB)

    Mosqueron, L.; Momas, I. [Universite Rene Descartes, Faculte des Sciences Pharmaceutiques et Biologiques, Lab. d' Hygiene et de Sante Publique, 75 - Paris (France); Le Moullec, Y. [Laboratoire d' Hygiene de la Ville de Paris, 75 (France); Momas, I. [Direction de l' Action Sociale, de l' Enfance et de la Sante, Cellule Epidemiologie, 75 - Paris (France)

    2001-02-01

    There are few studies of individual exposure to atmospheric particles, because of the relatively bulky and noisy sampling devices. These personalized measurements, generally associated with micro-environmental measurements, are aimed at studying the distribution of individual exposure and identifying its main determinants. Methods: A synopsis of the methods implemented in such studies (populations studied, measurements strategies, questionnaires on time-activity patterns, residences and work place) was detailed. The major results are presented and discussed from an epidemiological point of view. Results: The individual exposure measured with portable devices generally were generally found to be higher than the estimations made by combining micro-environmental (outdoor and indoor) measurements and data from time-activity diaries. The difference between results of these two approaches, known as 'personal cloud', remains poorly understood. Correlations between individual measurements and outdoor concentrations are weak; nevertheless, day to day variations of these two series of measurements are better related. The main determinants of individual exposure to particles are identified but a quantification of their contribution remains difficult, except for passive smoking. Conclusion: Personal measurements cannot be used to estimate particle exposure in large scale epidemiological studies. This exposure needs to be modeled. (authors)

  1. 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

  2. Deuterated interstellar polycyclic aromatic hydrocarbons

    NARCIS (Netherlands)

    Peeters, E; Allamandola, LJ; Bauschlicher, CW; Hudgins, DM; Sandford, SA; Tielens, AGGM

    2004-01-01

    We report infrared spectral evidence of deuterated interstellar polycyclic aromatic hydrocarbons (PAHs). Two bands are detected in the infrared emission from the ionization bar in Orion at 4.4 and 4.65 mum. The one at 4.65 mum is present at the 4.4 sigma level, while the one at 4.4 mum is more

  3. Particulate Matter (PM) Pollution

    Science.gov (United States)

    ... Environmental Protection Agency Search Search Particulate Matter (PM) Pollution Contact Us Share Most PM particles form in ... and cause serious health effects. Particulate Matter (PM) Pollution PM Basics What is PM, and how does ...

  4. Optimization of collision/reaction gases for determination of 90Sr in atmospheric particulate matter by inductively coupled plasma tandem mass spectrometry after direct introduction of air via a gas-exchange device

    Science.gov (United States)

    Suzuki, Yoshinari; Ohara, Ryota; Matsunaga, Kirara

    2017-09-01

    Nuclear power plant accidents release radioactive strontium 90 (90Sr) into the environment. Monitoring of 90Sr, although important, is difficult and time consuming because it emits only beta radiation. We have developed a new analytical system that enables real-time analysis of 90Sr in atmospheric particulate matter with an analytical run time of only 10 min. Briefly, after passage of an air sample through an impactor, a small fraction of the sample is introduced into a gas-exchange device, where the air is replaced by Ar. Then the sample is directly introduced into an inductively coupled plasma tandem mass spectrometry (ICP-MS/MS) system equipped with a collision/reaction cell to eliminate isobaric interferences on 90Sr from 90Zr+, 89Y1H+, and 90Y+. Experiments with various reaction gas conditions revealed that these interferences could be minimized under the following optimized conditions: 1.0 mL min- 1 O2, 10.0 mL min- 1 H2, and 1.0 mL min- 1 NH3. The estimated background equivalent concentration and estimated detection limit of the system were 9.7 × 10- 4 and 3.6 × 10- 4 ng m- 3, respectively, which are equivalent to 4.9 × 10- 6 and 1.8 × 10- 6 Bq cm- 3. Recoveries of Sr in PM2.5 measured by real-time analysis compared to those obtained by simultaneously collection on filter was 53 ± 23%, and using this recovery, the detection limit as PM2.5 was estimated to be 3.4 ± 1.5 × 10- 6 Bq cm- 3. That is, this system enabled detection of 90Sr at concentrations < 5 × 10- 6 Bq cm- 3 even considering the insufficient fusion/vaporization/ionization efficiency of Sr in PM2.5.

  5. Gas-particle phase partitioning and particle size distribution of chlorinated and brominated polycyclic aromatic hydrocarbons in haze.

    Science.gov (United States)

    Jin, Rong; Zheng, Minghui; Yang, Hongbo; Yang, Lili; Wu, Xiaolin; Xu, Yang; Liu, Guorui

    2017-12-01

    Chlorinated and brominated polycyclic aromatic hydrocarbons (Cl/Br-PAHs) are emerging semi-volatile organic pollutants in haze-associated particulate matter (PM). Their gas-particle phase partitioning and distribution among PM fractions have not been clarified. Clarification would increase understanding of atmospheric behavior and health risks of Cl/Br-PAHs. In this study, samples of the gas phase and 4 PM phases (aerodynamic diameters (dae) > 10 μm, 2.5-10 μm, 1.0-2.5 μm, and distribution indicated that the Cl/Br-PAHs tended to adhere to fine particles. Over 80% of the Cl-PAHs and 70% of the Br-PAHs were associated with fine PM (dae particle phase partitioning and PM distribution of Cl/Br-PAHs when heating of buildings was required, which was associated with haze events, were obviously different from those when heating was not required. The relationship between the logarithmic geometric mean diameters of the Cl/Br-PAH congeners and reciprocal of the temperature (1/T) suggested that low air temperatures during the heating period could lead to high proportions of Cl/Br-PAHs in the fine particles. Increased coal burning during the heating period also contributed to high Cl/Br-PAH loads in the fine particles. Copyright © 2017 Elsevier Ltd. All rights reserved.

  6. Dispersion modeling of polycyclic aromatic hydrocarbons from combustion of biomass and fossil fuels and production of coke in Tianjin, China.

    Science.gov (United States)

    Tao, Shu; Li, Xinrong; Yang, Yu; Coveney, Raymond M; Lu, Xiaoxia; Chen, Haitao; Shen, Weiran

    2006-08-01

    A USEPA, procedure, ISCLT3 (Industrial Source Complex Long-Term), was applied to model the spatial distribution of polycyclic aromatic hydrocarbons (PAHs) emitted from various sources including coal, petroleum, natural gas, and biomass into the atmosphere of Tianjin, China. Benzo[a]pyrene equivalent concentrations (BaPeq) were calculated for risk assessment. Model results were provisionally validated for concentrations and profiles based on the observed data at two monitoring stations. The dominant emission sources in the area were domestic coal combustion, coke production, and biomass burning. Mainly because of the difference in the emission heights, the contributions of various sources to the average concentrations at receptors differ from proportions emitted. The shares of domestic coal increased from approximately 43% at the sources to 56% at the receptors, while the contributions of coking industry decreased from approximately 23% at the sources to 7% at the receptors. The spatial distributions of gaseous and particulate PAHs were similar, with higher concentrations occurring within urban districts because of domestic coal combustion. With relatively smaller contributions, the other minor sources had limited influences on the overall spatial distribution. The calculated average BaPeq value in air was 2.54 +/- 2.87 ng/m3 on an annual basis. Although only 2.3% of the area in Tianjin exceeded the national standard of 10 ng/m3, 41% of the entire population lives within this area.

  7. Seasonal and daily source apportionment of polycyclic aromatic hydrocarbon concentrations in PM10 in a semirural European area.

    Science.gov (United States)

    Van Drooge, Barend L; Pérez Ballesta, Pascual

    2009-10-01

    Polycyclic aromatic hydrocarbons (PAH) were analyzed from ambient air particulate matter (PM10) that was collected near Lago Maggiore (Lombardy) in Northern Italy from August 2008 to January 2009. Highest individual PAH concentrations ranged from 0.05 ng/m3 during mid-days in summer to about 6 ng/m3 duringthe nights of the coldest period. A multivariate experimental regression model for the estimation of PAH concentrations was used to apportion the identified local sources of PAHs. This model included specific markers (i.e., levoglucosan for wood combustion and hopanes for traffic emission) and meteorological parameters (i.e., ambient air temperature and atmospheric mixing layer heights). In autumn and winter, wood combustion on a daily average contributed from 30 to 70% to the PAHs in ambient air PM10. In this period, the contribution of the wood combustion was less than 30% during mid-day, increasing sometimes to more than 80% during the night In the samples taken during the summer period, traffic contribution to PAH concentrations was about 30%, while wood combustion was insignificant.

  8. FTIR analysis and evaluation of carcinogenic and mutagenic risks of nitro-polycyclic aromatic hydrocarbons in PM1.0.

    Science.gov (United States)

    Schneider, Ismael Luís; Teixeira, Elba Calesso; Agudelo-Castañeda, Dayana Milena; Silva E Silva, Gabriel; Balzaretti, Naira; Braga, Marcel Ferreira; Oliveira, Luís Felipe Silva

    2016-01-15

    Nitro-polycyclic aromatic hydrocarbons (NPAHs) represent a group of organic compounds of significant interest due to their presence in airborne particulates of urban centers, wide distribution in the environment, and mutagenic and carcinogenic properties. These compounds, associated with atmospheric particles of size Carcinogenic and mutagenic risks of the studied NPAHs associated with PM1.0 samples were also determined for two sampling sites: Canoas and Sapucaia do Sul. The results showed that NPAH standard spectra can effectively identify NPAHs in PM1.0 samples. The transmittance and emissivity sample spectra showed broader bands and lower relative intensity than the standard NPAH spectra. The carcinogenic risk and the total mutagenic risk were calculated using the toxic equivalent factors and mutagenic potency factors, respectively. Canoas showed the highest total carcinogenic risk, while Sapucaia do Sul had the highest mutagenic risk. The seasonal analysis suggested that in the study area the ambient air is more toxic during the cold periods. These findings might of significant importance for the decision and policy making authorities.

  9. Diurnal and nocturnal variations of PAHs in the Lhasa atmosphere, Tibetan Plateau: Implication for local sources and the impact of atmospheric degradation processing

    Science.gov (United States)

    Liu, Junwen; Li, Jun; Lin, Tian; Liu, Di; Xu, Yue; Chaemfa, Chakra; Qi, Shihua; Liu, Fobang; Zhang, Gan

    2013-04-01

    Due to the unique characteristics, such as intensive radiation, high altitude and low humidity, plateau climate importantly affects the airborne organic contaminants' behavior in the environment. In this study, USEPA priority polycyclic aromatic hydrocarbons (PAHs) and benzo[e]pyrene were detected in the air samples collected at two suburban sites in Lhasa city. The total concentrations of USEPA priority fifteen PAHs (except naphthalene) in the particulate phase ranged from 4.4 to 60 ng/m3, while in the gas phase from 79 to 350 ng/m3. Integrated results of the multiple diagnostic ratios indicated that the major potential sources of PAHs in Lhasa city were local incomplete combustion of wood and cow dung cake. Particulate and gaseous PAH levels in this study displayed two clear and different diurnal and nocturnal concentration patterns, however, no distinct diurnal and nocturnal variation was observed for the total suspended particles (TSP) concentrations. No significant correlation was found between TSP concentrations and particle-bound PAHs, meaning physicochemical processes play an important role in diurnal and nocturnal variations of PAHs in the atmosphere except emission sources in this study. Based on the diurnal and nocturnal changes of the percentage of particulate phase PAHs in total PAHs, it suggested that gas-particle partitioning driven by temperature makes a great contribution to the variations of PAHs concentrations. The most susceptible to transformation between gas and particle phase chemicals are PHE, ANT, FLA, PYR, BaA and CHR. In addition, our observation suggested that atmospheric reaction and photolytic degradation also exert an important impact on the variations of PAHs in both phases in the atmosphere of Lhasa city.

  10. Elemental Composition and Sources of Atmospheric Particulate ...

    African Journals Online (AJOL)

    An intensive aerosol field campaign was carried out from 16 August to 16 September 2005 (dry season) at a kerbside in Dar es Salaam, Tanzania. A Gent PM10 stacked filter unit sampler with coarse and fine Nuclepore polycarbonate filters, providing fine (0.4 μm) and coarse (8 μm) size fractions, was deployed. A total of 64 ...

  11. Elemental Composition of Atmospheric Particulate Matter during ...

    African Journals Online (AJOL)

    Five-day isentropic backward trajectories as determined by the air trajectory HYSPLIT model were computed for Morogoro and the allocated sector of oceanic origin over continental, mainly through Mozambique and Tanzania) was the most common. However, other sectors such as Oceanic, over Madagascar or continental ...

  12. Biotransformation of polycyclic aromatic hydrocarbons in marine polychaetes

    DEFF Research Database (Denmark)

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

    2008-01-01

    by including data obtained using analytical chemistry and molecular techniques. In marine polychaetes induction of CYP enzyme activity after exposure to PAHs and the mechanism behind this is currently not well established. Conflicting results regarding the inducibility of CYP enzymes from polychaetes have led......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...... about the mechanisms underlying elimination of accumulated PAHs. An important pathway of elimination is through biotransformation which results in increased aqueous solubility of the otherwise hydrophobic PAHs. Biotransformation in marine polychaetes proceeds in a two phased process similar to those...

  13. Simulated transport of polycyclic aromatic hydrocarbons in artificial streams

    Energy Technology Data Exchange (ETDEWEB)

    Bartell, S.M.; Landrum, P.F.; Giesy, J.P.; Leversee, G.J.

    1981-01-01

    A model was constructed to predict the pattern of flow and accumulation of three polycyclic aromatic hydrocarbons (PAH) (anthracene, naphthalene, and benzo(a)pyrene) in artificial streams located on the Savannah River Plant near Aiken, South Carolina. Predictions were based upon the premise that the fundamental chemistry of individual PAH contains useful information for predictive purposes. Model processes included volatilization, photolysis, sorption to sediments and particulates, and net accumulation by biota. Simulations of anthracene transport were compared to results of an experiment conducted in the streams. The model realistically predicted the concentration of dissolved anthracene through time and space. Photolytic degradation appeared to be a major pathway of anthracene flux from the streams.

  14. 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.

  15. Influence of traffic emissions on the carcinogenic polycyclic aromatic hydrocarbons in outdoor breathable particles.

    Science.gov (United States)

    Slezakova, Klara; Castro, Dionísia; Pereira, Maria C; Moralis, Simone; Delerue-Matos, Cristina; Alvim-Ferraz, Maria C

    2010-04-01

    Because polycyclic aromatic hydrocarbons (PAHs) have been proven to be toxic, mutagenic, and/or carcinogenic, there is widespread interest in analyzing and evaluating exposure to PAHs in atmospheric environments influenced by different emission sources. Because traffic emissions are one of the biggest sources of fine particles, more information on carcinogenic PAHs associated with fine particles needs to be provided. Aiming to further understand the impact of traffic particulate matter (PM) on human health, this study evaluated the influence of traffic on PM10 (PM with aerodynamic diameter carcinogenic PAHs. Samples were collected at one site influenced by traffic emissions and at one reference site using low-volume samplers. Analysis of PAHs was performed by microwave-assisted extraction combined with liquid chromatography (MAE-LC); 17 PAHs, including 9 carcinogenic ones, were quantified. At the site influenced by traffic emissions, PM10 and PM2.5 concentrations were, respectively, 380 and 390% higher than at the background site. When influenced by traffic emissions, the total concentration of nine carcinogenic compounds (naphthalene, chrysene, benzo(a)anthracene, benzo(b) fluoranthene, benzo(k)fluoranthene, benzo(a)pyrene, dibenzo(a,h)anthracene, indeno(1,2,3-cd)pyrene, and dibenzo(a,l)pyrene) was increased by 2400 and 3000% in PM10 and PM2.5, respectively; these nine carcinogenic compounds represented 68 and 74% of total PAHs (sigma(PAHs)) for PM10 and PM2.5, respectively. All PAHs, including the carcinogenic compounds, were mainly present in fine particles. Considering the strong influence of these fine particles on human health, these conclusions are relevant for the development of strategies to protect public health.

  16. Emission characteristics and size distribution of polycyclic aromatic hydrocarbons from coke production in China

    Science.gov (United States)

    Mu, Ling; Peng, Lin; Liu, Xiaofeng; He, Qiusheng; Bai, Huiling; Yan, Yulong; Li, Yinghui

    2017-11-01

    Coking is regarded as a major source of atmospheric polycyclic aromatic hydrocarbons (PAHs), but few researches have been conducted on the emission characteristics of PAHs from coke production. In this study, emissions of size-segregated particulate matter (PM) and particle-bound PAHs emitted from charging of coal (CC) and pushing of coke (PC) in four typical coke plants were determined. The emission factors on average, sums of CC and PC, were 4.65 mg/kg, 5.96 mg/kg, 19.18 μg/kg and 20.69 μg/kg of coal charged for PM2.1 (≤ 2.1 μm), PM, PAHs in PM2.1 and total-PAHs, respectively. PM and PAHs emission from plants using stamp charging were significantly more than those using top charging. The profile of PAHs in PM with size ≤ 1.4 μm (PM1.4) emitted from CC process were similar with that from PC, however, it revealed obviously different tendency for PAHs in PM with size > 1.4 μm, indicating the different formation mechanism for coarse particles emitted from CC and PC. Size distributions of PM and PAHs indicated that they were primarily connected with PM1.4, and the contributions of PM1.4 to PM and PAHs emitted from the plants using stamp charging were higher than those using top charging. Some improved technology in air-pollution control devices should be considered in coke production in future based on the considerable impacts of PM1.4 and PAHs on human health and ambient air quality.

  17. 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

  18. The study of azaarene behavior over atmosphere of subtropical city(Keelung)

    Science.gov (United States)

    Liu, Chih Yun

    2017-04-01

    In this study, we collected the Total Suspended Particulates (TSP) from July 2014 to February 2016 in the subtropical city (Keelung), and researched azaarene behavior over atmosphere. Polycyclic Aromatic Compounds (PAHs) are ubiquitous pollutants in the environment; they have known carcinogens and/or mutagens, mainly produce from incomplete combustion. Azaarenes are polycyclic aromatic hydrocarbon derivative compounds in which a carbon atom in one of the aromatic rings is substituted by a nitrogen atom. Organism exposure to azaarenes occurs through inhalation of polluted air and by ingestion of food and/or water containing combustion products and accumulate in the body. Total azaarene concentration (16 individual compound concentration of the aggregate) is between 0.92 to 3.76 μg/m3, results showed that the concentration of azaarenes have significant seasonal variation, they have higher concentration in the cold month. In molecular weight, the highest proportion is the molecular weight equal to 143(ΣMQ) and then the molecular weight equal to 179(BAP), ΣMQ would rise from 30% 40% to 40% 50% during the cold month and warm months. Compared to ring number, 2-rings are biggest part, the smallest is 4-rings, its ratio has slight variation, but primary species is 2-rings. Emissions from transportation, local housing heating, factories burning fossil fuels and dust from Mainland south air mass are pollutant, their sources and climate conditions can affect concentration and composition of compound. There are highly significant correlation between 3-rings and 4-rings, which suggests that there are similar source strengths and transport mechanisms for these compounds. Correlation between concentration of azaarenes and ambient temperature is negative moderation, with concentration of atmospheric suspended particles is positive moderate correlation. Finally, we establish the relationship between the three parameters to predict concentration of azaarenes over atmosphere of

  19. Polycyclic aromatic hydrocarbons (PAHs) in ambient aerosols from Beijing: characterization of low volatile PAHs by positive-ion atmospheric pressure photoionization (APPI) coupled with Fourier transform ion cyclotron resonance.

    Science.gov (United States)

    Jiang, Bin; Liang, Yongmei; Xu, Chunming; Zhang, Jingyi; Hu, Miao; Shi, Quan

    2014-05-06

    Aromatic fractions derived from aerosol samples were characterized by gas chromatography and mass spectrometry (GC-MS), high temperature simulated distillation (SIMDIS), and positive-ion atmospheric pressure photoionization (APPI) Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS), respectively. It was found that about 27 wt % compounds in aromatic fractions could not be eluted from a GC column and some large molecule PAHs were neglected in GC-MS analysis. APPI FT-ICR MS was proven to be a powerful approach for characterizing the molecular composition of aromatics, especially for the large molecular species. An aromatic sample from Beijing urban aerosol was successfully characterized by APPI FT-ICR MS. Results showed that most abundant aromatic compounds in PM2.5 (particles with aerodynamic diameter ≤ 2.5 μm) were highly condensed hydrocarbons with 4-8 aromatic rings and their homologues with very short alkyl chains. Furthermore, heteroatom-containing hydrocarbons were found as the significant components of the aromatic fractions: O1, O2, N1, and S1 class species with 10-28 DBEs (double bond equivalents) and 14-38 carbon numbers were identified by APPI FT-ICR MS. The heteroatom PAHs had similar DBEs and carbon number distribution as regular PAHs.

  20. [Distribution characteristics of particulate mercury in aerosol in coastal city].

    Science.gov (United States)

    Zhang, Fu-Wang; Zhao, Jin-Ping; Chen, Jin-Sheng; Xu, Ya

    2010-10-01

    Particulate mercury, which is bound with aerosol in atmosphere, has a negative impact on human health and the environment, also plays an important role in the biogeochemical process of mercury. In this paper, taking southeast coastal city of Xiamen as research object, the PM2.5, PM10 and TSP were collected in residential, tourism, industrial area and background, respectively, during four seasons (October 2008-September 2009). RA-915 + mercury analyzer was employed to determinate mercury concentration in different size particle matters based on zeeman atomic absorption spectrometry. The results showed that the contents of particulate mercury in different size of aerosol during Winter, Spring were obviously higher than that of Summer, Autumn; the concentrations of particulate mercury in fine particle during Spring, Summer, Autumn and Winter were (51.46 +/- 19.28), (42.41 +/- 12.74), (38.38 +/- 6.08) and (127.23 +/- 33.70) pg/m3, respectively. The experimental data showed that the particulate mercury were mainly distributed in fine particles (PM2.5), which covered 42.48%-67.87%, and it can be concluded that the rate of particulate mercury enrichment in coarse particle was much lower than that of fine particle. The sequence of atmospheric particulate mercury concentration in different functional areas was: background tourism < industrial area < suburban; which showed characteristics of spatial distribution of particulate mercury was affected by the sampling location. On the whole, Xiamen had a low level of atmospheric particulate mercury; the enrichment of PM2.5 to particulate mercury was significantly higher than that of PM10 and TSP, and showed that fine particle pollution should be tightly controlled to reduce particulate mercury.

  1. Global distribution and Gas-particle Partitioning of Polycyclic Aromatic Hydrocarbons - a Modelling Study

    Science.gov (United States)

    Lammel, G.; Sehili, A. M.

    2009-04-01

    Polycyclic aromatic hydrocarbons (PAHs) are emitted in all combustion processes. Some undergo re-volatilisation (multi-hopping). Little is known about degradation pathways and the processes determining gas-particle partitioning (Lohmann & Lammel, 2004). Distribution and fate have no been studied on the global scale so far (except for emissions in Europe and Russia; Sehili & Lammel, 2007). Anthracene (ANT), fluoranthene (FLT) and benzo[a]pyrene (BAP) have been studied under present-day climate and each 3 scenarios of atmospheric degradation and gas-particle partitioning using an atmospheric general circulation model with embedded dynamic aerosol submodel, ECHAM-HAM (Stier et al., 2005) and re-volatilization from ground compartments (Semeena et al., 2006). 10 years were simulated with a time-step of 30 min and 2.8°x2.8° and 19 levels. Emissions were compiled based on emission factors in 27 major types of combustion technologies, scaled to 141 combustion technologies and their global distribution as of 1996 (1°x1°) according to fuel type and the PM1 emission factor (Bond et al., 2004). The emissions were entried uniformly throughout the entire simulation time. Scenarios tested: AD = adsorption (according to the Junge empirical relationship; Pankow, 1987), OB = absorption in organic matter and adsorption to soot (Lohmann & Lammel, 2004) without and DP = with degradation in the atmospheric particulate phase. Gas-particle partitioning in air influences drastically the atmospheric cycling, total environmental fate (e.g. compartmental distributions) and the long-range transport potential (LRTP) of the substances studied. The LRTP is mostly regional. Comparison with observed levels indicate that degradation in the particulate phase must be slower than in the gas-phase. Furthermore, the levels of semivolatile PAHs (ANT and FLT) at high latitudes and a European mid latitude site cannot be explained by partitioning due to adsorption alone, but point to both absorption into

  2. 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...

  3. Particle phase distribution of polycyclic aromatic hydrocarbons in stormwater — Using humic acid and iron nano-sized colloids as test particles

    DEFF Research Database (Denmark)

    Nielsen, Katrine; Kalmykova, Yuliya; Strömvall, Ann-Margret

    2015-01-01

    fraction was found in the sample with occurrence of small nano-sized particles (b10 nm). The results show the importance of developing technologies that both can manage particulate matter and effectively remove PAHs present in the Colloidal and Dissolved fractions in stormwater. © 2015 Elsevier B.V. All......The distribution of polycyclic aromatic hydrocarbons (PAHs) in different particulate fractions in stormwater: Total, Particulate, Filtrated, Colloidal and Dissolved fractions, were examined and compared to synthetic suspensions of humic acid colloids and iron nano-sized particles. The distribution......, surprisingly, high loads were found in the Dissolved fractions. The PAHs identified in stormwater in the Particulate fractions and Dissolved fractions follow their hydrophobic properties. In most samples N50% of the HMW PAHs were found in the Particulate fractions, while the LMW and MMW PAHs were found...

  4. 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

  5. Photodynamic activity of polycyclic hydrocarbon

    Energy Technology Data Exchange (ETDEWEB)

    Epstein, S.S.

    1963-01-01

    Exposure of Paramecium caudatum to suspensions of 3,4-benzopyrene, followed by long wave ultraviolet irradiation, results in cell death at times related, inter alia, to carcinogen concentration. Prior to death, the cells exhibit progressive immobilization and blebbing. This photodynamic response is a sensitized photo-oxidation, as it is oxygen-dependent and inhibited by anti-oxidants, such as butylated hydroxy anisole and ..cap alpha..-tocopherol. Protection is also afforded by other agents, including Tweens, tryptophan and certain fractions of plasma proteins. No evidence was found for the involvement of peroxides or sulfhydryl groups. The correlations between photodynamic toxicity and carcinogenicity in a large series of polycyclic hydrocarbons is under investigation. Assays of air extracts for photodynamic toxicity are in progress. Significant toxicity has been found in oxygenated besides aromatic fractions.

  6. Determination of carcinogenic polycyclic aromatic hydrocarbons ...

    African Journals Online (AJOL)

    Determination of carcinogenic polycyclic aromatic hydrocarbons (pahs), anthracene in different variety of fish samples in the Bangsai river of Bangladesh. F Yeasmin, SMM Rahman, S Rana, KJ Fatema, MA Hossain ...

  7. Infrared Spectra of Polycyclic Aromatic Hydrocarbons (PAHs)

    Science.gov (United States)

    Bauschlicher, Charles W., Jr.; Bakes, E. L. O.

    2000-01-01

    We have computed the synthetic infrared spectra of some polycyclic aromatic hydrocarbons containing up to 54 carbon atoms. The species studied include ovalene, circumcoronene, dicoronylene, and hexabenzocoronene. We report spectra for anions, neutrals, cations, and multiply charged cations.

  8. Inhalation Cancer Risk Associated with Exposure to Complex Polycyclic Aromatic Hydrocarbon Mixtures in an Electronic Waste and Urban Area in South China

    Science.gov (United States)

    Wang, Jing; Chen, Shejun; Tian, Mi; Zheng, Xiaobo; Gonzales, Leah; Ohura, Takeshi; Mai, Bixian; Simonich, Staci L. Massey

    2012-01-01

    Atmospheric particulate matter samples were collected from May 2010 to April 2011 in a rural e-waste area and in Guangzhou, South China, to estimate the lifetime inhalation cancer risk from exposure to parent polycyclic aromatic hydrocarbons (PAHs), high molecular weight PAHs (MW 302 PAHs), and halogenated PAHs (HPAHs). Seasonal variations in the PAH concentrations and profile within and between the e-waste and urban areas indicated different PAH sources in the two areas. Benzo[b]fluoranthene, BaP, dibenz[ah]anthracene, and dibenzo[al]pyrene made the most significant contribution to the inhalation cancer risk. MW 302 PAHs accounting for 18.0% of the total cancer risk in the e-waste area and 13.6% in the urban area, while HPAHs made a minor contribution (e-waste area and from 9.3 to 737 per million people in Guangzhou. PAH exposure accounted for 0.02 to 1.94% of the total lung cancer cases in Guangzhou. On average, the inhalation cancer risk in the e-waste area was 1.6 times higher than in the urban area. The e-waste dismantling activities in South China led to higher inhalation cancer risk due to PAH exposure than the urban area. PMID:22913732

  9. Characterization of functional groups of airborne particulate matter

    Science.gov (United States)

    Baitimirova, M.; Katkevics, J.; Baumane, L.; Bakis, E.; Viksna, A.

    2013-12-01

    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).

  10. 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.

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

    Science.gov (United States)

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

    2017-07-01

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

  12. Using comprehensive GC × GC to study PAHs and n-alkanes associated with PM2.5 in urban atmosphere.

    Science.gov (United States)

    Xu, Tingting; Lv, Yan; Cheng, Tiantao; Li, Xiang

    2015-04-01

    Comprehensive two-dimensional gas chromatography (GC × GC) utilizing a flow modulator was applied to study particulate polycyclic aromatic hydrocarbons (PAHs) and n-alkanes in the urban atmosphere. Samples were collected onto quartz fiber filters using a PM2.5 sampler at Megacity Shanghai, China. Sample preparation included extraction into n-hexane-dichloromethane mixture and cleanup on silver-impregnated silica column. Analyses were performed well with GC × GC-FID and GC × GC-TOFMS equipment. Average particulate PAHs and n-alkane concentrations were in the range of 40-100 ng/m(3) and 120-500 pg/m(3), respectively. It is alarming to note that PAHs and n-alkane concentrations were increasing with urban PM2.5 values and exceeded the air quality standards in many sampling events. Among them, 2-ring, 3-ring, and 4-ring PAHs accounted for the majority of total PAHs, and C10-15 accounted for the majority of particulate n-alkanes. Potential sources of PAHs in PM2.5 were identified using the diagnostic ratios between PAHs. Local emission sources such as combustion from gasoline and diesel engines were the main contributors of particulate-associated PAHs, while long-range transport had minor contribution to the particulate PAHs. Additionally, we determined the overall carcinogenicity of the samples based on PAH concentrations by a dose addition model and found that the overall carcinogenicity during polluted period was obviously higher than during good air quality period.

  13. 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

  14. 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 ?

  15. Short-term impact of atmospheric pollution on fecundability.

    Science.gov (United States)

    Slama, Rémy; Bottagisi, Sébastien; Solansky, Ivo; Lepeule, Johanna; Giorgis-Allemand, Lise; Sram, Radim

    2013-11-01

    Epidemiologic studies have reported associations between air pollution levels and semen characteristics, which might in turn affect a couple's ability to achieve a live birth. Our aim was to characterize short-term effects of atmospheric pollutants on fecundability (the month-specific probability of pregnancy among noncontracepting couples). For a cohort of births between 1994 and 1999 in Teplice (Czech Republic), we averaged fine particulate matter (PM2.5), carcinogenic polycyclic aromatic hydrocarbons, ozone, nitrogen dioxide (NO2), and sulfur dioxide levels estimated from a central measurement site over the 60-day period before the end of the first month of unprotected intercourse. We estimated changes in the probability of occurrence of a pregnancy during the first month of unprotected intercourse associated with exposure, using binomial regression and adjusting for maternal behaviors and time trends. Among the 1,916 recruited couples, 486 (25%) conceived during the first month of unprotected intercourse. Each increase of 10 µg/m in PM2.5 levels was associated with an adjusted decrease in fecundability of 22% (95% confidence interval = 6%-35%). NO2 levels were also associated with decreased fecundability. There was no evidence of adverse effects with the other pollutants considered. Biases related to pregnancy planning or temporal trends in air pollution were unlikely to explain the observed associations. In this polluted area, we highlighted short-term decreases in a couple's ability to conceive in association with PM2.5 and NO2 levels assessed in a central monitoring station.

  16. Particulate matters from diesel engine exhaust emission

    Directory of Open Access Journals (Sweden)

    Petrović Velimir S.

    2008-01-01

    Full Text Available Air pollution caused by diesel engine emissions, especially particulate matters and nitric oxides emissions, is one of the biggest problems of current transportation. In the near future the emission of diesel particulate matters will become one of the most important factors that will affect the trend of engine development. Ambient airborne particles have adverse environmental and health effects and therefore their concentration in the air is regulated. Recent medical studies showed that different particle properties are important (for example: number/concentration, active surface, chemical composition/morphology and may take role in the responsibility for their human health impact. Thus, diesel engines are one of the most important sources of particles in the atmosphere, especially in urban areas. Studying health effects and diesel engine particulate properties, it has been concluded that they are a complex mixture of solids and liquids. Biological activity of particulate matter may be related to particle sizes and their number. The paper presents the activities of UN-ECE working group PMP on defining the best procedure and methodology for the measurement of passenger cars diesel engines particle mass and number concentrations. The results of inter-laboratory emissions testing are presented for different engine technologies with special attention on repeatability and reproducibility of measured data. .

  17. 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.

  18. 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 (< 0.10 um). The major emission sources of PAHs are open burning, industrial boilers and emission from cars and trucks. Emission rates of PAHs vary significantly depending on vehicle use: fuel type, engine type and catalytic 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

  19. Composição elementar do material particulado presente no aerossol atmosférico do município de Sete Lagoas, Minas Gerais Elemental composition of the particulate matter present in the atmospheric aerosols of Sete Lagoas, MG

    Directory of Open Access Journals (Sweden)

    Paula Guimarães Moura Queiroz

    2007-10-01

    Full Text Available The main objective of this study was the identification of sources generating particulate matter in the atmospheric aerosols of Sete Lagoas, Minas Gerais. The measurement of the mineral composition was accomplished by X-ray diffractometry and the elemental concentration by neutron activation analysis. The results showed that Al, Cl, Cu, Fe, K, Mg and Na are the predominant chemical elements in the total suspended particles (TPS. The presence of Na, Ba, Cl, Cu, Eu, Fe and Sm in those particles with aerodynamic diameter smaller than 10 µm (PM10, indicates that soil dust and ceramic and pig iron industries are the main sources of air quality degradation in the region.

  20. 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

  1. 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)

  2. 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.

  3. Dry Deposition of Polycyclic Aromatic Hydrocarbons (PAHs) at a Suburban Site in Beijing, China

    Science.gov (United States)

    Zhang, Xincheng; Wang, Weiyu; Zhu, Xianlei

    2017-04-01

    A great amount of polycyclic aromatic hydrocarbons (PAHs) have been generated by industrial production, waste incineration and landfill, traffic and road dust etc. They are emitted into atmosphere and afterwards enter into water body and soil through deposition, resulting in wide distribution of PAHs in environment. However, the dry deposition of PAHs from atmosphere has not been well studied, especially in the aspects of its characteristics, environmental and health effects, sources and mechanism. This study measured PAHs dry deposition in the northwest suburban area of Beijing. Dry deposition samples (i.e. dustfall samples) were collected at the sampling site located in China University of Petroleum - Beijing in 2012-2016. And PAHs in the samples were determined by GC/MS. The dry deposition flux of 16 US EPA priority PAHs (ΣPAH16) was 2.58 μg/(m^2·d), which was lower than those in other regions of North China. Its seasonal variability was more significant than annual variability (p spring > autumn > summer. The amount of ΣPAH16 removed from the atmosphere by dry deposition process accounted for only 1.2% of their emissions, indicating that the atmosphere self-purification capacity was quite limited and emission reduction measures would play a key role in controlling PAHs air pollution. However, PAHs dry deposition would deteriorate soil quality since the content of ΣPAH16 in dustfall was 1-2 orders of magnitude higher than that in soil in the same area. Dermal exposure resulting from PAHs dry deposition was not the major route. The sources of PAHs dry deposition varied with seasons. The profile and specific ratios of PAHs showed that in winter, domestic coal combustion was the main source of PAHs with the contribution up to 77%; in spring and summer, the impact of coal combustion decreased and the contribution of vehicle exhaust increased to 30% - 45%; in fall, in addition to coal combustion and vehicle exhaust, the impact of biomass burning was observed

  4. NICKEL SPECIATION OF URBAN PARTICULATE MATTER

    Energy Technology Data Exchange (ETDEWEB)

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

    2003-10-01

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

  5. Semivolatile particulate organic material in southern Africa during SAFARI 2000

    Science.gov (United States)

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

    2003-07-01

    During August and September 2000, the University of Washington's (UW) Cloud and Aerosol Research Group (CARG) with its Convair-580 research aircraft participated in the Southern African Fire-Atmosphere Research Initiative (SAFARI) 2000 field study in southern Africa. Aboard this aircraft was a Particle Concentrator-Brigham Young University Organic Sampling System (PC-BOSS), which was used to determine semivolatile particulate material with a diffusion denuder sampler. Denuded quartz filters and sorbent beds in series were used to measure nonvolatile and semivolatile materials, respectively. Results obtained with the PC-BOSS are compared to those obtained with conventional quartz-quartz and Teflon-quartz filter pack samplers. Various 10-120 min integrated samples were collected during flights through the free troposphere, in the atmospheric boundary layer, and in plumes from savanna fires. Significant fine particulate semivolatile organic compounds (SVOC) were found in all samples. The SVOC was not collected by conventional filter pack samplers and therefore would not have been determined in previous studies that used only filter pack samplers. The SVOC averaged 24% of the fine particulate mass in emissions from the fires and 36% of the fine particulate mass in boundary layer samples heavily impacted by aged emissions from savanna fires. Concentrations of fine particulate material in the atmospheric mixed layer heavily impacted by aged savanna fire emissions averaged 130 μg m-3. This aerosol was 85% carbonaceous material.

  6. Semivolatile Particulate Organic Material Southern Africa during SAFARI 2000

    Science.gov (United States)

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

    2005-01-01

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

  7. Air-sea exchange and gas-particle partitioning of polycyclic aromatic hydrocarbons over the northwestern Pacific Ocean: Role of East Asian continental outflow.

    Science.gov (United States)

    Wu, Zilan; Lin, Tian; Li, Zhongxia; Jiang, Yuqing; Li, Yuanyuan; Yao, Xiaohong; Gao, Huiwang; Guo, Zhigang

    2017-11-01

    We measured 15 parent polycyclic aromatic hydrocarbons (PAHs) in atmosphere and water during a research cruise from the East China Sea (ECS) to the northwestern Pacific Ocean (NWP) in the spring of 2015 to investigate the occurrence, air-sea gas exchange, and gas-particle partitioning of PAHs with a particular focus on the influence of East Asian continental outflow. The gaseous PAH composition and identification of sources were consistent with PAHs from the upwind area, indicating that the gaseous PAHs (three-to five-ring PAHs) were influenced by upwind land pollution. In addition, air-sea exchange fluxes of gaseous PAHs were estimated to be -54.2-107.4 ng m(-2) d(-1), and was indicative of variations of land-based PAH inputs. The logarithmic gas-particle partition coefficient (logKp) of PAHs regressed linearly against the logarithmic subcooled liquid vapor pressure (logPL(0)), with a slope of -0.25. This was significantly larger than the theoretical value (-1), implying disequilibrium between the gaseous and particulate PAHs over the NWP. The non-equilibrium of PAH gas-particle partitioning was shielded from the volatilization of three-ring gaseous PAHs from seawater and lower soot concentrations in particular when the oceanic air masses prevailed. Modeling PAH absorption into organic matter and adsorption onto soot carbon revealed that the status of PAH gas-particle partitioning deviated more from the modeling Kp for oceanic air masses than those for continental air masses, which coincided with higher volatilization of three-ring PAHs and confirmed the influence of air-sea exchange. Meanwhile, significant linear regressions between logKp and logKoa (logKsa) for PAHs were observed for continental air masses, suggesting the dominant effect of East Asian continental outflow on atmospheric PAHs over the NWP during the sampling campaign. Copyright © 2017 Elsevier Ltd. All rights reserved.

  8. High Diversity of Fungi in Air Particulate Matter

    Science.gov (United States)

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

    2009-04-01

    Fungal spores account for large proportions of air particulate matter, and they influence the hydrological cycle and climate as nuclei for water droplets and ice crystals in clouds, fog and precipitation. Moreover, some fungi are major pathogens and allergens. The diversity of airborne fungi is, however, hardly known. By DNA analysis we found pronounced differences in the relative abundance and seasonal cycles of various groups of fungi in coarse and fine particulate matter, with more plant pathogens in the coarse and more human pathogens and allergens in the respirable fine particle fraction (fungi to primary biogenic aerosols in the atmosphere: wet and dry discharged spores, carbohydrates, and inorganic ions, Atmospheric Chemistry and Physics, 7, 4569-4588, 2007. Fröhlich-Nowoisky, J. Despres, V.R., Pöschl, U.: High diversity of fungi in air particulate matter, Proceedings of the National Academy of Sciences, submitted, 2008.

  9. Predicting the Biodegradation of Polycyclic Aromatic Hydrocarbons ...

    African Journals Online (AJOL)

    This study investigates the prediction of biodegradation of polycyclic aromatic hydrocarbons using a mixture of naphthalene; anthracene and pyrene in a continuously stirred tank reactor by an artificial neural network. Artificial neural networks are relatively crude electronic networks of "neurons" whose operations are based ...

  10. Toxic Potential of Carcinogenic Polycyclic Aromatic Hydrocarbons ...

    African Journals Online (AJOL)

    DR. GODSON

    Toxic Potential of Carcinogenic Polycyclic Aromatic Hydrocarbons (cPAHs) and Heavy. Metal in Crude Oil from Gokana Area, Rivers State, Nigeria. *1. IWUOHA, G;. 1. ORUBITE, O;. 1. OKITE I. 1Department of Pure and Industrial Chemistry, Faculty of Sciences, University of Port Harcourt. ABSTRACT: This article is focused ...

  11. Polycyclic aromatic hydrocarbons (PAHs) contamination in coastal ...

    African Journals Online (AJOL)

    The objective of this study was to determine the levels of polycyclic aromatic hydrocarbons (PAHs) in sediments and crabs in the mangrove ecosystems of Zanzibar. Sediments and crabs from eight sampling sites were analysed for eleven selected PAHs. Samples were extracted with dichloromethane by ultrasonication, ...

  12. short communication aliphatic and polycyclic aromatic hydrocarbons ...

    African Journals Online (AJOL)

    Preferred Customer

    The compositional pattern of the photo-modified bitumen samples suggests that there was initial cracking of large molecular mass hydrocarbons in the bitumen, followed by recombination after long periods of exposure to sunlight. The polycyclic aromatic hydrocarbon profile of the Agbabu natural bitumen as a function of.

  13. 6 Polycyclic Aromatic Hydrocarbons.cdr

    African Journals Online (AJOL)

    Administrator

    Polycyclic aromatic hydrocarbons (PAHs) concentrations were measured by gas chromatography with flame ionization detector (GC/FID) in two fish species, Sardinella maderensis (Flat sardinella) and Galeoides decadactylus (Lesser African threadfin or Shine-nose or Common threadfin) from Ghanaian coastal waters and.

  14. Bioremediation of Polycyclic Aromatic Hydrocarbon contaminated ...

    African Journals Online (AJOL)

    This study investigates the effect of lead and chromium on the rate of bioremediation of polycyclic aromatic hydrocarbon (PAH) contaminated clay soil. Naphthalene was used as a target PAH. The soil was sterilized by heating at 120oC for one hour. 100g of the soil was contaminated with lead, chromium, nickel and mercury ...

  15. Remediation of soil contaminated with polycyclic aromatic ...

    African Journals Online (AJOL)

    The aim of this study was to determine ways of remediating soils contaminated with polycyclic aromatic hydrocarbons (PAHs) associated with crude oil. The study involves the use of planted cowpeas, mushrooms, algae, dead vegetable and live earthworm, and fire-heating of the contaminated garden soil collected from the ...

  16. Aliphatic and polycyclic aromatic hydrocarbons profiles of ...

    African Journals Online (AJOL)

    The impact of sunlight on aliphatic and polycyclic aromatic hydrocarbons profiles of Agbabu natural bitumen in Nigeria was investigated. The raw flow type of the bitumen was purified and exposed to sunlight for six consecutive months. Different portions of the bitumen were withdrawn at an interval of one month and were ...

  17. SPATIAL VARIATION AND DISTRIBUTION OF POLYCYCLIC ...

    African Journals Online (AJOL)

    An investigative study on polycyclic aromatic hydrocarbons (PAHs) in soils of different sampling stations in Effurun metropolis and its environs of the Niger Delta Area of Nigeria was carried out with gas chromatography mass spectrometry (GC-MS). Among the 16 US EPA priority PAHs determined, pyrene was observed to ...

  18. Prevalence of polycyclic aromatic hydrocarbons (PAHs) degrading ...

    African Journals Online (AJOL)

    Recalcitrant pollutants such as polycyclic aromatic hydrocarbons (PAHs) are difficult to degrade and have been the focus for biodegradation. They form a class of pollutant on a global scale. In an attempt to contribute to the search for suitable microbial culture with potential to biodegrade low and high molecular weight PAHs ...

  19. Polycyclic aromatic hydrocarbons (PAHs) degradation by laccase ...

    African Journals Online (AJOL)

    Laccase enzyme was produced from an isolate of the white rot fungus, Ganoderma lucidum Chaaim-001 BCU. The enzyme was subsequently evaluated for its degradative ability towards sixteen types of polycyclic aromatic hydrocarbons (PAHs). The G. lucidum laccase degraded antracene completely with or without a ...

  20. Measurements of Polycyclic Aromatic Hydrocarbons and ...

    African Journals Online (AJOL)

    This research was designed to examine the presence of polycyclic aromatic hydrocarbons (PAHs) in soot deposited at the Mariannhill toll plaza situated on the N3 highway in KwaZulu-Natal, South Africa. Samples were collected from the toll plaza either by scraping the toll booth walls and surrounding areas, or by wiping ...

  1. VIIRSN Level-3 Standard Mapped Image, Particulate Inorganic Carbon, Monthly, 4km

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — NOAA CoastWatch distributes Particulate Inorganic Carbon data from ther NPP-Suomi spacecraft. Measurements are gathered by VIIRS instrument carried aboard the...

  2. VIIRSN Level-3 Standard Mapped Image, Particulate Organic Carbon, 8-Day, 4km

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — NOAA CoastWatch distributes Particulate Organic Carbon data from the NPP-Suomi Spacecraft Measurements are gathered by the VIIRS instrument carried aboard the...

  3. Emission characteristics of polycyclic aromatic hydrocarbons and nitro-polycyclic aromatic hydrocarbons from diesel trucks based on on-road measurements

    Science.gov (United States)

    Cao, Xinyue; Hao, Xuewei; Shen, Xianbao; Jiang, Xi; Wu, Bobo; Yao, Zhiliang

    2017-01-01

    Polycyclic aromatic hydrocarbon (PAH) and nitro-polycyclic aromatic hydrocarbon (NPAH) emissions from 18 diesel trucks of different sizes and with different emission standards were tested in Beijing using a portable emission measurement system (PEMS). Both the gaseous- and particulate-phase PAHs and NPAHs were quantified by high-performance liquid chromatography (HPLC) in the laboratory. The emission factors (EFs) of the total PAHs from light-duty diesel trucks (LDDTs), medium-duty diesel trucks (MDDTs) and heavy-duty diesel trucks (HDDTs) were 82229.11 ± 41906.06, 52867.43 ± 18946.47 and 93837.35 ± 32193.14 μg/km, respectively, much higher than the respective values of total NPAHs from their counterpart vehicles. The gaseous phase had an important contribution to the total PAHs and NPAHs, with a share rate of approximately 69% and 97% on average, respectively. The driving cycle had important impacts on the emissions of PAHs and NPAHs, especially for LDDTs and HDDTs. Higher emissions of PAHs and NPAHs were detected on non-highway roads compared to that on highways for these two types of vehicles. Compared to the results of different studies, the difference in the EFs of PAHs and NPAHs can reach several orders of magnitudes, which would introduce errors in the development of an emission inventory of PAHs and NPAHs.

  4. Rigid particulate matter sensor

    Science.gov (United States)

    Hall, Matthew [Austin, TX

    2011-02-22

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

  5. 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.

  6. 40 CFR 60.102 - Standard for particulate matter.

    Science.gov (United States)

    2010-07-01

    ... Refineries § 60.102 Standard for particulate matter. Each owner or operator of any fluid catalytic cracking... which the fluid catalytic cracking unit catalyst regenerator will be operated, or 180 days after initial... discharge or cause the discharge into the atmosphere from any fluid catalytic cracking unit catalyst...

  7. Development of two fine particulate matter standard reference materials (<4 μm and <10 μm) for the determination of organic and inorganic constituents.

    Science.gov (United States)

    Schantz, Michele M; Cleveland, Danielle; Heckert, N Alan; Kucklick, John R; Leigh, Stefan D; Long, Stephen E; Lynch, Jennifer M; Murphy, Karen E; Olfaz, Rabia; Pintar, Adam L; Porter, Barbara J; Rabb, Savelas A; Vander Pol, Stacy S; Wise, Stephen A; Zeisler, Rolf

    2016-06-01

    Two new Standard Reference Materials (SRMs), SRM 2786 Fine Particulate Matter (Particulate Matter (particulate matter (PM). These materials have been characterized for the mass fractions of selected polycyclic aromatic hydrocarbons (PAHs), nitrated PAHs, brominated diphenyl ether (BDE) congeners, hexabromocyclododecane (HBCD) isomers, sugars, polychlorinated dibenzo-p-dioxin (PCDD) and dibenzofuran (PCDF) congeners, and inorganic constituents, as well as particle-size characteristics. These materials are the first Certified Reference Materials available to support measurements of both organic and inorganic constituents in fine PM. In addition, values for PAHs are available for RM 8785 Air Particulate Matter on Filter Media. As such, these SRMs will be useful as quality control samples for ensuring compatibility of results among PM monitoring studies and will fill a void to assess the accuracy of analytical methods used in these studies. Graphical Abstract Removal of PM from filter for the preparation of SRM 2786 Fine Particulate Matter.

  8. Transport of terrigenous polycyclic aromatic hydrocarbons affected by the coastal upwelling in the northwestern coast of South China Sea.

    Science.gov (United States)

    Ya, Miaolei; Wu, Yuling; Li, Yongyu; Wang, Xinhong

    2017-10-01

    Coastal upwelling prevails in the coast of Hainan Island, the northern South China Sea (SCS) during summer. We studied the influences of the upwelling on the horizontal and vertical transport of terrigenous polycyclic aromatic hydrocarbons (PAHs). PAHs in dissolved and suspended particulate phase of water samples were determined in the upper (depth  10 m). PAH levels decreased sharply from inshore to offshore to open sea. The results showed that terrestrial input was the main source of coastal PAHs. Perylene, an important indicator of land plant-derived PAH, showed the significant correlation with PAHs (p sea. Copyright © 2017 Elsevier Ltd. All rights reserved.

  9. 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.

  10. 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

  11. 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

  12. Enantioselective Thiourea-Catalyzed Cationic Polycyclizations

    Science.gov (United States)

    Knowles, Robert R.; Lin, Song

    2010-01-01

    A new thiourea catalyst is reported for the enantioselective cationic polycyclization of hydroxylactams. Both the yield and enantioselectivity of this transformation were found to vary strongly with the identity of a single aromatic residue on a common catalyst framework, with more expansive and polarizable arenes proving optimal. Evidence is presented for a mechanism in which stabilizing cation-π interactions are a principal determinant of enantioselectivity. PMID:20369901

  13. Development of the GC-MS organic aerosol monitor (GC-MS OAM) for in-field detection of particulate organic compounds

    Science.gov (United States)

    Cropper, Paul M.; Overson, Devon K.; Cary, Robert A.; Eatough, Delbert J.; Chow, Judith C.; Hansen, Jaron C.

    2017-11-01

    Particulate matter (PM) is among the most harmful air pollutants to human health, but due to its complex chemical composition is poorly characterized. A large fraction of PM is composed of organic compounds, but these compounds are not regularly monitored due to limitations in current sampling and analysis techniques. The Organic Aerosol Monitor (GC-MS OAM) combines a collection device with thermal desorption, gas chromatography and mass spectrometry to quantitatively measure the carbonaceous components of PM on an hourly averaged basis. The GC-MS OAM is fully automated and has been successfully deployed in the field. It uses a chemically deactivated filter for collection followed by thermal desorption and GC-MS analysis. Laboratory tests show that detection limits range from 0.2 to 3 ng for 16 atmospherically relevant compounds, with the possibility for hundreds more. The GC-MS OAM was deployed in the field for semi-continuous measurement of the organic markers, levoglucosan, dehydroabietic acid, and polycyclic aromatic hydrocarbons (PAHs) from January to March 2015. Results illustrate the significance of this monitoring technique to characterize the organic components of PM and identify sources of pollution.

  14. Atmospheric PAHs, NPAHs, and OPAHs at an urban, mountainous, and marine sites in Northern China: Molecular composition, sources, and ageing

    Science.gov (United States)

    Zhang, Junmei; Yang, Lingxiao; Mellouki, Abdelwahid; Chen, Jianmin; Chen, Xiangfeng; Gao, Ying; Jiang, Pan; Li, Yanyan; Yu, Hao; Wang, Wenxing

    2018-01-01

    18 gaseous and particulate polycyclic aromatic hydrocarbons (PAHs), 16 nitro-derivative (NPAHs), and 7 oxy-derivative (OPAHs) were analyzed by Gas Chromatography-Mass Spectrometry (GC-MS) at three locations in Northern China, an urban site (Jinan), a marine site (Tuoji island), and a mountain site (Mt. Tai). The combined gas and particulate concentrations of 18 PAHs, 16 NPAHs, and 7 OPAHs were highest at the urban site (305.91, 2.80, and 9.05 ng/m3, respectively) and lowest at the mountain location (37.83, 0.27, and 1.59 ng/m3, respectively). A noticeable increase in the high molecular weight PAHs was observed during polluted conditions compared to clean conditions. Diagnostic ratios clearly demonstrated that coal/biomass combustion was the major PAH source in Northern China. The particulate PAHs were the most aged at the mountain site due to long-distance atmospheric transport. The formation rate of NPAHs was most efficient at the mountain location and during heavily polluted days at the urban and marine sites. In addition, the main formation pathway for NPAHs was through the OH initiated secondary reaction. NO3 radicals most significantly contributed to the NPAHs formation at night, during clear weather, and at the mountain site. The logKp value was lowest at the urban site for most individual compounds and highest at the mountain site. Higher logKp was found for NPAHs and OPAHs compared with their corresponding parent PAHs. The linear regression of logKp vs logPL0 at the three sites suggested that the gas-particle partitioning of PAHs might be in non-equilibrium.

  15. Airborne polycyclic aromatic hydrocarbons trigger human skin cells aging through aryl hydrocarbon receptor.

    Science.gov (United States)

    Qiao, Yuan; Li, Qiang; Du, Hong-Yang; Wang, Qiao-Wei; Huang, Ye; Liu, Wei

    2017-07-01

    Accumulating evidence suggests that polycyclic aromatic hydrocarbons (PAH) which adsorbed on the surface of ambient air particulate matters (PM), are the major toxic compound to cause cardiovascular and respiratory diseases, even cancer. However, its detrimental effects on human skin cell remain unclear. Here, we demonstrated that SRM1649b, a reference urban dust material of PAH, triggers human skin cells aging through cell cycle arrest, cell growth inhibition and apoptosis. Principally, SRM1649b facilitated Aryl hydrocarbon receptor (AhR) translocated into nucleus, subsequently activated ERK/MAPK signaling pathway, and upregulated aging-related genes expression. Most important, we found that AhR antagonist efficiently revert the aging of skin cells. Thus our novel findings firstly revealed the mechanism of skin aging under PAH contamination and provided potential strategy for clinical application. Copyright © 2017. Published by Elsevier Inc.

  16. Atmospheric Change on Pluto

    Science.gov (United States)

    Person, Michael

    2013-10-01

    We propose to use SOFIA with HIPO and FLITECAM (FLIPO) to measure the parameters of Pluto's atmosphere (temperature, pressure, possible particulate haze) by observing a stellar occultation by Pluto on 15 November 2014. Due to its highly elliptical orbit and seasonally variable obliquity, Pluto's atmosphere is predicted to condense onto its surface within the next ~10 years and possibly within the next few years and thus frequent observations are critical. Detection of the occultation central flash will allow measurement of the structure of Pluto's lower atmosphere and atmospheric oblateness. We will use FLIPO to measure the refracted starlight contemporaneously at visible and infrared wavelengths; this approach is needed to differentiate between two competing explanations for the deficiency in the observed light refracted from Pluto's lower atmosphere (strong thermal gradients versus variable particulate extinction). Only an airborne platform such as SOFIA has the flexibility to place a large telescope in the center of the shadow path of this brief event while at the same time nearly eliminating the possibility of missing time-critical observations due to unfortunate weather systems. Occultation predictions will be updated throughout the period preceding the observations with the goal of achieving sufficient prediction accuracy at the event time to place SOFIA directly in the path of Pluto's central flash. This SOFIA observation will be combined with our ongoing ground-based observing program whose goal is to measure the temporal variability of Pluto's atmosphere in response to its changing seasonal obliquity (and resulting ice migration) and recession from the sun. For the NASA New Horizons mission to Pluto and the Kuiper Belt, this Pluto occultation event represents the last chance, prior to the spacecraft closest approach to the Pluto/Charon system (July 2015), to provide input to the mission for encounter planning, as well as context and supporting atmospheric

  17. Cytotoxicity and genotoxicity properties of particulate matter fraction 2.5 μm

    Science.gov (United States)

    Bełcik, Maciej K.; Trusz-Zdybek, Agnieszka; Zaczyńska, Ewa; Czarny, Anna; Piekarska, Katarzyna

    2017-11-01

    In the ambient is more than 2,000 chemical substances, some of them are absorbed on the surface of the particulate matter and may causes many health problems. Air pollution is responsible for more than 3.2 million premature deaths which classifies it as a second place environmental risk factor. Especially dangerous for health are polycyclic aromatic hydrocarbons and their nitro- and amino derivatives which shows mutagenic and carcinogenic properties. Air pollutions were also classified by International Agency for Research on Cancer to group which carcinogenic properties on human were proved by available knowledge. Air pollutions, including particulate matter are one of the biggest problem in Polish cities. World Health Organization in report published in May 2016 set many of Polish cities on the top of the list most polluted in European Union. The article presents results of mutagenicity, genotoxicity and cytotoxicity researches conducted on a particulate matter fraction 2.5 μm collected during all year long in Wroclaw agglomeration. The material were collected on filters using high-flow air aspirator and extracted using dichloromethane. Additionally it was fractionated into 2 parts containing: all pollutants and only polycyclic aromatic hydrocarbons. Dry residue of this fractions were dissolving in DMSO and tested using biological methods. Biological methods include mutagenicity properties which are investigated by Salmonella assay (Ames assay). Other biological method was comet assay and 4 parameter cytotoxicity test PAN-I assay. Results of the conducted experiments shows differences in mutagenic, genotoxic and cytotoxic properties between seasons of collection and between volume of dust pollutions fractions. The worst properties shows particles collected in autumn and winter season and this containing only polycyclic aromatics hydrocarbons. Results showed also some correlations in results obtained during different methods and properties.

  18. 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.

  19. Emission factors for carbonaceous particles and polycyclic aromatic hydrocarbons from residential coal combustion in China

    Energy Technology Data Exchange (ETDEWEB)

    Yingjun Chen; Guoying Sheng; Xinhui Bi; Yanli Feng; Bixian Mai; Jiamo Fu [Chinese Academy of Sciences, Guangzhou (China). State Key Laboratory of Organic Geochemistry

    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 {mu}m. 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. 61 refs., 5 tabs.

  20. 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.

  1. Impact of partitioning and oxidative processing of PAH in fogs and clouds on atmospheric lifetimes of PAH

    Science.gov (United States)

    Eagar, Jershon Dale; Ervens, Barbara; Herckes, Pierre

    2017-07-01

    The importance of the atmospheric aqueous phase of fogs and clouds, for the processing and removal of polycyclic aromatic hydrocarbons (PAHs) is not well known. A multiphase model was developed to determine the fate and lifetime of PAHs in fogs and clouds for a limited set of daytime conditions. The model describes partitioning between three phases (aqueous, liquid organic, and gas), experimental and estimated (photo)oxidation rates. Using a limited set of microphysical and chemical input conditions, the loss rates of PAHs in the complex three-phase system are explored. At 25 °C, PAHs with two, three and four rings are predicted to be primarily in the gas phase (fraction in the gas phase xg > 90%) while five- and six-ring PAHs partition significantly into droplets with aqueous phase fractions of 1-6% and liquid organic phase fractions of 31-91%, respectively. The predicted atmospheric chemical lifetimes of PAHs in the presence of fog or cloud droplets (<8 h) are significantly shorter than literature predictions of PAH lifetimes due to wet and dry deposition (1-14 days and 5-15 months, respectively) and shorter than or equal to predicted lifetimes due to chemical reactions in the gas and organic particulate phases (1-300 h). Even though PAH solubilities are ≤4 × 10-2 g L-1, the results of the current study show that often the condensed phase of fog and cloud droplets cannot be neglected as a PAH sink.

  2. Particle phase distribution of polycyclic aromatic hydrocarbons in stormwater--Using humic acid and iron nano-sized colloids as test particles.

    Science.gov (United States)

    Nielsen, Katrine; Kalmykova, Yuliya; Strömvall, Ann-Margret; Baun, Anders; Eriksson, Eva

    2015-11-01

    The distribution of polycyclic aromatic hydrocarbons (PAHs) in different particulate fractions in stormwater: Total, Particulate, Filtrated, Colloidal and Dissolved fractions, were examined and compared to synthetic suspensions of humic acid colloids and iron nano-sized particles. The distribution of low-molecular weight PAHs (LMW PAHs), middle-molecular weight PAHs (MMW PAHs) and high-molecular weight PAHs (HMW PAHs) among the fractions was also evaluated. The results from the synthetic suspensions showed that the highest concentrations of the PAHs were found in the Filtrated fractions and, surprisingly, high loads were found in the Dissolved fractions. The PAHs identified in stormwater in the Particulate fractions and Dissolved fractions follow their hydrophobic properties. In most samples >50% of the HMW PAHs were found in the Particulate fractions, while the LMW and MMW PAHs were found to a higher extent in the Filtrated fractions. The highest concentrations of PAHs were present in the stormwater with the highest total suspended solids (TSS); the relative amount of the HMW PAHs was highest in the Particulate fractions (particles>0.7 μm). The highest concentration of PAHs in the Colloidal fraction was found in the sample with occurrence of small nano-sized particles (importance of developing technologies that both can manage particulate matter and effectively remove PAHs present in the Colloidal and Dissolved fractions in stormwater. Copyright © 2015 Elsevier B.V. All rights reserved.

  3. Effects on ambient air caused by emissions from the Clean Harbors incinerator and underground water treatment facility in Mercier : evaluation by atmospheric dispersion modeling; Effets sur l'air ambiant des emissions de l'incinerateur Clean Harbors et de l'Unite de traitement des eaux souterraines (UTES) a Mercier : evaluation par modelisation de la dispersion atmospherique

    Energy Technology Data Exchange (ETDEWEB)

    Boulet, G.; Walsh, P.; Brault, M.P.; Couture, Y.; Briere, J.F. [Quebec Ministere du Developpement durable, de l' Environnement et des Parcs, Quebec, PQ (Canada). Direction du suivi de l' etat de l' environnement; Guay, F.; Longpre, L. [Quebec Ministere du Developpement durable, de l' Environnement et des Parcs, Quebec, PQ (Canada). Direction regionale de l' analyse et de l' expertise de l' Estrie de la Monteregie; Lemire, R.; Busque, D. [Quebec Ministere du Developpement durable, de l' Environnement et des Parcs, Quebec, PQ (Canada). Service de l' information sur le milieu atmospherique

    2010-09-15

    Clean Harbors is a leading provider of high-tech, high-temperature destruction of hazardous and industrial waste. The Quebec Ministry of Sustainable Development, Environment and Parks created an atmospheric dispersion model to determine the impact of the Clean Harbors incinerator and underground water treatment facility on air quality in Mercier, Quebec. This document described the dispersion model and its inputs, including emissions of polychlorinated dibenzodioxin, dibenzofurans, polychlorinated biphenyls, polycyclic aromatic hydrocarbons, fine particulates, mercury, lead and arsenic. The effects of these emissions on air quality were evaluated by considering meteorological data, source characteristics, topography and land use zoning. The modeling study showed that emissions from the incinerator were well below criteria levels and do not cause significant deterioration in air quality. However, higher than allowable limits of polyvinyl chloride and benzene emissions were found 700 m from the underground water treatment facility. Nearby residential areas were not affected. 21 refs., 9 tabs., 10 figs., 1 appendix.

  4. Air pollution from a large steel factory: polycyclic aromatic hydrocarbon emissions from coke-oven batteries.

    Science.gov (United States)

    Liberti, Lorenzo; Notarnicola, Michele; Primerano, Roberto; Zannetti, Paolo

    2006-03-01

    A systematic investigation of solid and gaseous atmospheric emissions from some coke-oven batteries of one of Europe's largest integrated steel factory (Taranto, Italy) has been carried out. In air monitoring samples, polycyclic aromatic hydrocarbons (PAHs) were consistently detected at concentrations largely exceeding threshold limit values. By means of PAHs speciation profile and benzo(a)pyrene (BaP) equivalent dispersion modeling from diffuse sources, the study indicated that serious health risks exist not only in working areas, but also in a densely populated residential district near the factory.

  5. A review on polycyclic aromatic hydrocarbons: Source, environmental impact, effect on human health and

    Directory of Open Access Journals (Sweden)

    Hussein I. Abdel-Shafy

    2016-03-01

    The aim of this review is to discuss PAHs impact on the environmental and the magnitude of the human health risks posed by such substances. They also contain important information on concentrations, burdens and fate of polycyclic aromatic hydrocarbons (PAHs in the atmosphere. The main anthropogenic sources of PAHs and their effect on the concentrations of these compounds in air are discussed. The fate of PAHs in the air, their persistence and the main mechanisms of their losses are presented. Health hazards associated with PAH air pollution are stressed.

  6. Characteristics of organic compounds in aerosol particulate matter from Dhahran city, Saudi Arabia

    Directory of Open Access Journals (Sweden)

    Ahmed I. Rushdi

    2017-05-01

    Full Text Available Organic chemical pollutants in atmospheric particulate matter (PM have a potential toxicity hazard resulting in human responses that vary from no discernible effect to premature death. The formation and sources of PM also affect air quality of metropolitan areas as well as climate change. The new developments and industrial activities in the Middle East, especially Saudi Arabia, are expected to contribute to the natural, regional, and anthropogenic input sources of organic matter (OM. Here we report the occurrence, concentrations and sources of organic tracers, including n-alkanes, polycyclic aromatic hydrocarbons (PAHs, plasticizers, and petroleum biomarkers, in ambient atmospheric PM from the city of Dhahran, Saudi Arabia. The major compounds were unresolved complex mixtures (UCM of branched and cyclic hydrocarbons (489 ± 296 ng m−3, plasticizers (131 ± 119 ng m−3 for phenyl phosphates, 87 ± 42 ng m−3 for phthalates, n-alkanes (73 ± 53 ng m−3, hopane biomarkers (11 ± 8 ng m−3, n-alkanones (6.7 ± 6.3 ng m−3, PAHs (2.0 ± 2.1 ng m−3, n-alkanols (1.2 ± 1.2 ng m−3, sterane biomarkers (0.4 ± 0.3 ng m−3, and sterols (0.5 ± 0.4 ng m−3. Obviously, UCM and plasticizers were the major components (56 ± 9% and 26 ± 10% of the total extracts, respectively in the PM of Dhahran, which might have adverse public health effects. The major sources of this OM are emissions from industrial factories north of the city, plastics and biomass burning, and petroleum product combustion (traffic/refining.

  7. Emissions of particle-phase polycyclic aromatic hydrocarbons (PAHs) in the Fu Gui-shan Tunnel of Nanjing, China

    Science.gov (United States)

    Chen, Fei; Hu, Wei; Zhong, Qin

    2013-04-01

    Real-world vehicle emission factors for PM10 (particulate matter with aerodynamic diameter smaller than 10 μm) and particle-phase polycyclic aromatic hydrocarbons (PAHs) from mixed vehicles were quantified in the Fu Gui-shan Tunnel of Nanjing during summer and winter of 2010. Concentrations of PM10 and sixteen particle phase polycyclic aromatic hydrocarbons (PAHs) in the entrance and exit of the tunnel were studied. The results showed that the four most abundant particular phase polycyclic aromatic hydrocarbons (PAHs) of motor vehicle were benzo[ghi]perylene, benzo[k]fluoranthene, benz[a]anthracene and benzo[a]pyrene. The emission factors for PM10 and particle-phase PAHs were 687 mg veh- 1 km- 1 and 18.853 mg veh- 1 km- 1 in summer, 714 mg veh- 1 km- 1 and 20.374 mg veh- 1 km- 1 in winter. Higher particle-phase PAH emission factors were found to be associated with a high proportion of diesel-fueled vehicles (DV). The estimated PM10 emission factor of gasoline-fueled vehicles (GV) was 513 mg veh- 1 km- 1 and the value for DV was 914 mg veh- 1 km- 1, while EFDV of particulate PAH (31.290 mg veh- 1 km- 1) was nearly 4 times higher than EFGV (9.310 mg veh- 1 km- 1). The five highest emission factors of diesel-fueled vehicles (DV) were benzo[ghi]perylene, benzo[k]fluoranthene, Indeno[1,2,3-cd]pyrene, benz[a]anthracene and benzo[a]pyrene, which was similarly found in the gasoline-fueled vehicles (GV). The sum of these five emission factors accounted for ~ 69% of the total particle-phase PAH of DV and ~ 67% of GV.

  8. 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

  9. Staging atmospheres

    DEFF Research Database (Denmark)

    Bille, Mikkel; Bjerregaard, Peter; Sørensen, Tim Flohr

    2015-01-01

    The article introduces the special issue on staging atmospheres by surveying the philosophical, political and anthropological literature on atmosphere, and explores the relationship between atmosphere, material culture, subjectivity and affect. Atmosphere seems to occupy one of the classic...

  10. Identifying and dating buried micropodzols in Subatlantic polycyclic drift sands

    NARCIS (Netherlands)

    Wallinga, J.; Mourik, van J.M.; Schilder, M.L.M.

    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

  11. Biodegradation of polycyclic aromatic hydrocarbons (PAHs) by white ...

    African Journals Online (AJOL)

    Biodegradation of polycyclic aromatic hydrocarbons (PAHs) by white rot-fungus Pseudotrametes gibbosa isolated from the boreal forest in Northeast China. ... This study provides technical support for pollution amelioration using aboriginal white-rot fungus. Key words: White-rot fungus, laccase, polycyclic aromatic ...

  12. Estimation of gas-particle partitioning coefficients (Kp) of carcinogenic polycyclic aromatic hydrocarbons in carbonaceous aerosols collected at Chiang-Mai, Bangkok and Hat-Yai, Thailand.

    Science.gov (United States)

    Pongpiachan, Siwatt; Ho, Kin Fai; Cao, Junji

    2013-01-01

    To assess environmental contamination with carcinogens, carbonaceous compounds, water-soluble ionic species and trace gaseous species were identified and quantified every three hours for three days at three different atmospheric layers at the heart of Chiang-Mai, Bangkok and Hat-Yai from December 2006 to February 2007. A DRI Model 2001 Thermal/Optical Carbon Analyzer with the IMPROVE thermal/optical reflectance (TOR) protocol was used to quantify the organic carbon (OC) and elemental carbon (EC) contents in PM10. Diurnal and vertical variability was also carefully investigated. In general, OC and EC mass concentration showed the highest values at the monitoring period of 21.00-00.00 as consequences of human activities at night bazaar coupled with reduction of mixing layer, decreased wind speed and termination of photolysis at nighttime. Morning peaks of carbonaceous compounds were observed during the sampling period of 06:00-09:00, emphasizing the main contribution of traffic emission in the three cities. The estimation of incremental lifetime particulate matter exposure (ILPE) raises concern of high risk of carbonaceous accumulation over workers and residents living close to the observatory sites. The average values of incremental lifetime particulate matter exposure (ILPE) of total carbon at Baiyoke Suit Hotel and Baiyoke Sky Hotel are approximately ten times higher than those air samples collected at Prince of Songkla University Hat-Yai campus corpse incinerator and fish-can manufacturing factory but only slightly higher than those of rice straw burning in Songkla province. This indicates a high risk of developing lung cancer and other respiratory diseases across workers and residents living in high buildings located in Pratunam area. Using knowledge of carbonaceous fractions in PM10, one can estimate the gas-particle partitioning of polycyclic aromatic hydrocarbons (PAHs). Dachs-Eisenreich model highlights the crucial role of adsorption in gas

  13. Seasonal Variation of Atmospheric Composition of Water-Soluble ...

    African Journals Online (AJOL)

    `123456789jkl''''#

    dust dispersion and biomass burning made a significant contribution to the atmospheric particulate pollution in. Morogoro. Keywords: Ion chromatography; Aerosol Characterization; coarse, fine and PM10 fractions; Meteorology. Introduction here is an increasing awareness of the influence of ambient particulate matter (PM) ...

  14. 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.

  15. 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

  16. Occurrence and photostability of 3-nitrobenzanthrone associated with atmospheric particles

    DEFF Research Database (Denmark)

    Feilberg, A.; Ohura, T.; Nielsen, T.

    2002-01-01

    of nitrated polycyclic aromatic hydrocarbons (nitro-PAHs) and other air pollution components, it is suggested that 3-nitrobenzanthrone is a directly emitted primary pollutant and that it is not formed in the atmosphere to a significant degree. The photodegradation of 3-nitrobenzanthrone was studied in order...

  17. Characterization of the particulate matter and relationship between buccal micronucleus and urinary 1-hydroxypyrene levels among cashew nut roasting workers.

    Science.gov (United States)

    de Oliveira Galvão, Marcos Felipe; de Queiroz, Jana Dara Freires; Duarte, Ediclê de Souza Fernandes; Hoelzemann, Judith Johanna; de André, Paulo Afonso; Saldiva, Paulo Hilário Nascimento; Menezes Filho, José Antônio; Batistuzzo de Medeiros, Silvia Regina

    2017-01-01

    The present study is the first assessment of occupational risk associated with artisanal cashew nut roasting using exposure and effect biomarkers, as well as a characterization and dispersion analysis of the released particulate matter (PM). A real-time particle monitor was used to quantify PM1.0, PM2.5 and PM10. Furthermore, the PM was sampled using a Handi-vol sampler, and the physicochemical characteristics were determined by SEM-EDS analysis. Trajectories, dispersion and deposition of the emitted material were calculated using the NOAA-HYSPLIT model. Urinary 1-hydroxypyrene (1-OHP) levels were analyzed by HPLC. DNA damage, chromosomal instability and cell death were measured by a buccal micronucleus cytome assay (BMCyt). The PM concentrations for all measurements in the exposed area were higher than in the non-exposed area. SEM-EDS analyses exhibited a wide variety of particles, and K, Cl, S and Ca biomass burning tracers were the major inorganic compounds. In addition, atmospheric modeling analysis suggested that these particles can reach regions farther away than 40 kilometers. Occupational polycyclic aromatic hydrocarbon exposure was confirmed by increases in 1-OHP levels in cashew nut workers. Frequencies of BMCyt biomarkers of genotoxicity (micronuclei and nuclear bud) and cytotoxicity (pyknosis, karyolysis, karyorrhexis and condensed chromatin) were higher in the exposed group compared with the controls. The influence of factors, such as age, on the micronuclei frequencies was demonstrated, and a correlation between 1-OHP and micronuclei was observed. To the best of our knowledge, no other study has demonstrated a correlation between these types of biomarkers. The use of exposure (1-OHP) and effect (BMCyt) biomarkers were therefore efficient in assessing the occupational risk associated with artisanal cashew nut roasting, and the high rates of PM2.5 are considered to be a potential contributor to this effect. Copyright © 2016 The Authors. Published by

  18. 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

    2016-08-02

    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 ( 5.5 were found in line with those commonly found for slowly or very slowly desorbing sediment-associated contaminants. PAHs with log Kow < 5.5 were found at higher desorbing rates. The addition of detergents did not influence the extractability of lighter PAHs but increased desorption rates for the heavier PAHs, potentially contributing to increases in the toxicity of tunnel-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.

  19. 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.

  20. Particulate matter and neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Otoshi, Tsunehiko [Tohoku Univ. of Community Service and Science, Sakata, Yamagata (Japan)

    2003-03-01

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

  1. 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...

  2. Recent developments in particulate control

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2013-01-04

    Electrostatic precipitators (ESP) are the dominant type of particulate control in pulverised coal combustion (PCC) plant; fabric filters (FF) play a smaller role. Environmental pressures and subsequent tighter regulations have lowered emission limit values (ELV) for particulate matter from PCC plant, and they are now extending to specific toxic metals, such as mercury. Lower ELV are generally met by increasing the efficiency of the existing particulate control via numerous enhancements. However, the existing fleet is ageing, various restrictions on site limit what work can be done and PCC plant is progressively operating under non-design conditions. Despite this, further developments in technology have led to significant improvements in collection efficiency and regulations have been met. New hybrid ESP/FF systems aim to become more viable than the individual technology by utilising the advantages of both technologies. The purpose of this report is to review the technical and economic considerations of enhancements in particulate control for PCC plant over the last decade.

  3. 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 few...

  4. Discuss on Satellite-Based Particulate Matter Monitoring Technique

    OpenAIRE

    Li, B; Hou, L.

    2015-01-01

    Satellite measurements for atmospheric pollutants monitoring provide full mapping, large spatial coverage, and high spatial resolution. Retrieved aerosol optical depth (AOD) from satellite data as the key parameter has been used in the study on particulate matter (PM) distributions which is complementary to ground-based measurements. Based on the empirical relations between aerosol optical properties and PM10 or PM2.5 concentration and its influencing factors, combining the Beijing-T...

  5. Electrical diesel particulate filter (DPF) regeneration

    Science.gov (United States)

    Gonze, Eugene V; Ament, Frank

    2013-12-31

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

  6. Elemental composition of arctic particulate matter

    Science.gov (United States)

    Cahill, T. A.; Eldred, R. A.

    1984-01-01

    Measurements were made of the elemental composition of particulate matter collected in flights in the Arctic in spring 1983 as part of the Arctic Gas and Aerosol Sampling Program (AGASP). Ten samples of size-selected particles were analyzed by four nondestructive techniques at Davis. Concentrations were determined for H, C, N, and O by Forward Alpha Scattering Techniques (FAST) and for elements heavier than fluorine by Particle Induced X-ray Emission (PIXE). Total mass was measured gravimetrically, and optical absorption was measured using the Laser Integrating Plate Method (LIPM). Results of the analyses show dramatic differences in concentrations and elemental ratios from the Alaskan Arctic to the Norwegian Arctic, with indications of wood smoke and sulfuric acid in the arctic atmosphere.

  7. 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.

  8. 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.

  9. Association between photodynamic and carcinogenic activities in polycyclic compounds

    Energy Technology Data Exchange (ETDEWEB)

    Epstein, S.S.; Small, M.; Falk, H.L.; Mantel, N.

    1964-06-01

    The photodynamic activities of 157 polycyclic compounds of wide structural range were determined, with the use of Paramecium caudatum. High photodynamic activity was largely confined to polycyclic compounds, either homocyclic or heterocyclic, with four or five fused rings. Significant absorption of light was shown to be prerequisite but not sufficient for high photodynamic activity. A significant statistical association between photodynamic activity and carcinogenicity was demonstrated. It was shown that compounds with high photodynamic activity had 4 times greater odds of being carcinogenic than compounds with low activity. However, the photodynamic assay cannot identify a particular polycyclic compound as being carcinogenic or noncarcinogenic.

  10. 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.

  11. 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.

  12. Polycyclic Aromatic Hydrocarbons in Urban Stream Sediments

    Directory of Open Access Journals (Sweden)

    Jejal Reddy Bathi

    2012-01-01

    Full Text Available Polycyclic aromatic hydrocarbons (PAHs are persistent organic pollutants of high environmental concern with known carcinogenic activity. Although literature documents PAH fate in urban runoff, little is known about their distribution on sediment sizes, which is essential for determining their treatability and fate in receiving waters. This paper has quantified the concentrations of selected PAHs in urban creek sediments and examined possible relationships between sediment PAH content and sediment characteristics, such as particle size, volatile organic content (VOC, and sediment chemical oxygen demand (SCOD. SCOD, VOC, and PAH concentrations of sediments showed a bimodal distribution by particle size. The large diameter sediments had the highest VOC and also had the highest PAH concentrations. The spatial variation of PAH content by sediment sizes also was statistically significant; however, the mass of the PAH material was significantly affected by the relative abundance of the different particle size classes in the sediment mixtures.

  13. Polycyclic aromatic hydrocarbons (PAHs) in yogurt samples.

    Science.gov (United States)

    Battisti, Chiara; Girelli, Anna Maria; Tarola, Anna Maria

    2015-01-01

    The concentrations and distributions of major polycyclic aromatic hydrocarbons (PAHs) were determined in 20 kinds of yogurt specimens collected from Italian supermarkets using reversed phase high-performance liquid chromatography equipped with fluorescence detection. The method was validated by determination of recovery percentages, precision (repeatability) and sensitivity (limits of detection) with yogurt samples fortified at 0.25, 0.5 and 1 µg/kg concentration levels. The recovery of 13 PAHs, with the exception of naphthalene and acenaphthene, ranged from 61% to 130% and from 60% to 97% at all the levels for yogurts with low (0.1%) and high (3.9%) fat content, respectively. The method is repeatable with relative standard deviation values yogurts with low and high fats were compared.

  14. Overview of Polycyclic Aromatic Compounds (PAC)

    Science.gov (United States)

    Achten, Christine; Andersson, Jan T.

    2015-01-01

    The chemical group of polycyclic aromatic compounds (PAC), including the better-known subgroup of polycyclic aromatic hydrocarbons (PAH) and the heterocyclic aromatic compounds (NSO-PAC, heterocycles), comprise several thousand individual compounds. It is hard to find a comprehensive overview in the literature of these PACs that includes a substantial amount of relevant properties. Here an attempt is made to summarize the most studied but also some less well-known PACs. In addition to basic data such as recommended names, abbreviations, CAS numbers, molecular formulas, chemical structures, and exact mono-isotopic molecular weights, physico-chemical properties taken from the literature like boiling points, vapor pressures, water solubilities, Henry's Law constants, n-octanol-water partition coefficients (log KOW), and pKa are summarized. Selected toxicological data are listed indicating carcinogenic and mutagenic activity or effects on different organisms. PAC nomenclature is a complex topic, so suggestions for practical use are made. Regarding available data, estimated (instead of measured) values should be used with caution because considerable deviations from experimentally determined values can occur. For an enhanced understanding of the behavior of single PACs in comparison with each other, some of the properties mentioned above are plotted vs. the number of rings or the degree of alkylation. Also, some physico-chemical data are correlated with different functional groups as substituents of the PAHs. This article reveals that rather little is known about the less common PACs, e.g., higher molecular weight compounds, alkylated or otherwise substituted aromatics, for instance, keto-, oxo-, amino-, nitro-, cyano-PAHs, or some heterocyclic aromatic compounds, including their derivatives. It mirrors the limited state of knowledge about the variety of PACs that do not belong to the 16 EPA PAHs. PMID:26823644

  15. 20 Elemental Composition and Sources of Atmospheric Particulate ...

    African Journals Online (AJOL)

    `123456789jkl''''#

    Abstract. An intensive aerosol field campaign was carried out from 16 August to 16 September 2005 (dry season) at a kerbside in Dar es Salaam, Tanzania. A Gent PM10 stacked filter unit sampler with coarse and fine Nuclepore polycarbonate filters, providing fine (0.4 µm) and coarse (8 µm) size fractions, was deployed.

  16. 0 Elemental Composition of Atmospheric Particulate Matter during ...

    African Journals Online (AJOL)

    Michael Horsfall

    induced X-ray emission. (PIXE) spectrometry (Maenhaut and Cafmeyer,. 1998). However, it should be noted that the PIXE data for the lightest elements (Na and Mg) are not very reliable because of severe X-ray attention. The data for sodium and ...

  17. An assessment of common atmospheric particulate matter sampling ...

    African Journals Online (AJOL)

    USER

    728, November 2010. Available ... existing technologies use inertial impactors or dicho- tomous samplers as particle size separators that ..... elements measured during this study. Detection limits and analytical precision vary widely with analytical.

  18. 0 Elemental Composition of Atmospheric Particulate Matter during ...

    African Journals Online (AJOL)

    Michael Horsfall

    analysed for the PM mass by weighing. A further analysis was performed for 25 elements by particle-induced x-ray emission spectrometry. The results show that the concentrations of the heavy metals were lower than those for the elements of crustal origin. The data from PIXE analysis and enrichment factor (E.F.) calculation ...

  19. Evaluation of polycyclic aromatic hydrocarbons and some heavy ...

    African Journals Online (AJOL)

    Scomber scombrus), suya beef and plantain (Musa paradiasca) sold and consumed in Amassoma town were screened for the presence of 15 polycyclic aromatic hydrocarbons (PAHs). Concentration of chromium, lead and cadmium were also ...

  20. The formation of polycyclic hydrocarbons during smoking process of cheese

    Directory of Open Access Journals (Sweden)

    Arzu Akpinar-Bayizit

    2011-09-01

    Full Text Available The smoking process determines the characteristic flavour, odour, colour and texture of several cheese varieties. Some smoke compounds are known to have bacteriostatic and antioxidant effects, and may act as preservatives. Smoked cheese is appreciated by consumers due to its sensorial properties. However, with smoking process there is a risk of formation of toxic polycyclic aromatic hydrocarbons (PAHs. This review emphasises the occurrence of polycyclic hydrocarbons on smoked cheeses and their health impacts.

  1. Membrane Characteristics for Removing Particulates in PFC Wastes

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Gye Nam; Lee, Sung Yeol; Won, Hui Jun; Jung, Chong Hun; Oh, Won Zin; Park, Jin Ho [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2005-06-15

    Pc (Per fluorocarbon) decontamination process is one of best methods to remove hot particulate adhered at inside surface of hot cell and surface of equipment in hot cell. It was necessary to develop a particulate filtration equipment to reuse Pc solution used on Pc decontamination due to its high cost and to minimize the volume of second wastewater. Contamination characteristics of hot particulate were investigated and then a filtration process was presented to remove hot particulate in Pc solution generated through Pc decontamination process. The removal efficiency of Pvdf (Poly vinylidene fluoride), Pp (Polypropylene), Ceramic (Al{sub 2}O{sub 3}) filter showed more than 95%. The removal efficiency of Pvdf filter was a little lower than those of other kiters at same pressure (3 psi). A ceramic filter showed a higher removal efficiency with other filters, while a little lower flux rate than other filters. Due to inorganic composition, a ceramic filter was highly stable against radio nuclides in comparison with Pvdf and Pp membrane, which generate H{sub 2} gas in {alpha}-radioactivity atmosphere. Therefore, the adoption of ceramic filter is estimated to be suitable for the real nitration process.

  2. Dynamics of Atmospheric Waves In a Hazy Atmosphere: Implications for Titan and Pluto

    Science.gov (United States)

    Matcheva, Katia

    2017-10-01

    We present a dynamical model of atmospheric gravity waves propagating in a stable atmosphere in the presence of small-size particulates. We consider a two-way interaction: (i) the effect of atmospheric mass-loading on the propagation of the waves and (ii) the dynamical forcing of the haze particle motion in the presence of variable atmospheric winds. The model illustrates the effect on the vertical distribution of haze particles due to wave-induces vertical winds and wind gradients. The results are presented in the context of Titan’s atmosphere and Cassini observations.

  3. Do 16 Polycyclic Aromatic Hydrocarbons Represent PAH Air Toxicity?

    Science.gov (United States)

    Samburova, Vera; Zielinska, Barbara; Khlystov, Andrey

    2017-01-01

    Estimation of carcinogenic potency based on analysis of 16 polycyclic aromatic hydrocarbons (PAHs) ranked by U.S. Environmental Protection Agency (EPA) is the most popular approach within scientific and environmental air quality management communities. The majority of PAH monitoring projects have been focused on particle-bound PAHs, ignoring the contribution of gas-phase PAHs to the toxicity of PAH mixtures in air samples. In this study, we analyzed the results of 13 projects in which 88 PAHs in both gas and particle phases were collected from different sources (biomass burning, mining operation, and vehicle emissions), as well as in urban air. The aim was to investigate whether 16 particle-bound U.S. EPA priority PAHs adequately represented health risks of inhalation exposure to atmospheric PAH mixtures. PAH concentrations were converted to benzo(a)pyrene-equivalent (BaPeq) toxicity using the toxic equivalency factor (TEF) approach. TEFs of PAH compounds for which such data is not available were estimated using TEFs of close isomers. Total BaPeq toxicities (∑88BaPeq) of gas- and particle-phase PAHs were compared with BaPeq toxicities calculated for the 16 particle-phase EPA PAH (∑16EPABaPeq). The results showed that 16 EPA particle-bound PAHs underrepresented the carcinogenic potency on average by 85.6% relative to the total (gas and particle) BaPeq toxicity of 88 PAHs. Gas-phase PAHs, like methylnaphthalenes, may contribute up to 30% of ∑88BaPeq. Accounting for other individual non-EPA PAHs (i.e., benzo(e)pyrene) and gas-phase PAHs (i.e., naphthalene, 1- and 2-methylnaphthalene) will make the risk assessment of PAH-containing air samples significantly more accurate. PMID:29051449

  4. Airborne particulate in Varanasi over middle Indo-Gangetic Plain: variation in particulate types and meteorological influences.

    Science.gov (United States)

    Murari, Vishnu; Kumar, Manish; Mhawish, Alaa; Barman, S C; Banerjee, Tirthankar

    2017-04-01

    The variation in particulate mass and particulate types (PM 2.5 and PM 10 ) with respect to local/regional meteorology was analyzed from January to December 2014 (n = 104) for an urban location over the middle Indo-Gangetic Plain (IGP). Both coarser (mean ± SD; PM 10 161.3 ± 110.4 μg m -3 , n = 104) and finer particulates (PM 2.5 81.78 ± 66.4 μg m -3 ) revealed enormous mass loading with distinct seasonal effects (range: PM 10 12-535 μg m -3 ; PM 2.5 8-362 μg m -3 ). Further, 56% (for PM 2.5 ) to 81% (for PM 10 ) of monitoring events revealed non-attainment national air quality standard especially during winter months. Particulate types (in terms of PM 2.5 /PM 10 0.49 ± 0.19) also exhibited temporal variations with high PM 2.5 loading particularly during winter (0.62) compared to summer months (0.38). Local meteorology has clear distinguishing trends in terms of dry summer (March to June), wet winter (December to February), and monsoon (July to September). Among all the meteorological variables (average temperature, rainfall, relative humidity (RH), wind speed (WS)), temperature was found to be inversely related with particulate loading (r PM10 -0.79; r PM2.5 -0.87) while RH only resulted a significant association with PM 2.5 during summer (r PM10 0.07; r PM2.5 0.55) and with PM 10 during winter (r PM10 0.53; r PM2.5 0.24). Temperature, atmospheric boundary layer (ABL), and RH were cumulatively recognized as the dominant factors regulating particulate concentration as days with high particulate loading (PM 2.5 >150 μg m -3 ; PM 10 >260 μg m -3 ) appeared to have lower ABL (mean 660 m), minimum temperature (<22.6 °C), and high RH (∼79%). The diurnal variations of particulate ratio were mostly insignificant except minor increases during night having a high wintertime ratio (0.58 ± 0.07) over monsoon (0.34 ± 0.05) and summer (0.30 ± 0.07). Across the region, atmospheric visibility appeared to be inversely associated with

  5. 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

  6. 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...

  7. An overview of particulate emissions from residential biomass combustion

    Science.gov (United States)

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

    2018-01-01

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

  8. Particulate matter and preterm birth

    Science.gov (United States)

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

  9. 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.

  10. Particulate Matter: a closer look

    NARCIS (Netherlands)

    Buijsman E; Beck JP; Bree L van; Cassee FR; Koelemeijer RBA; Matthijsen J; Thomas R; Wieringa K; LED; MGO

    2005-01-01

    The summary in booklet form 'Fijn stof nader bekeken' (Particulate Matter: a closer look) , published in Dutch by the Netherlands Environmental Assessment Agency (MNP) and the Environment and Safety Division of the National Institute for Public Health and the Environment (RIVM), has been designed to

  11. PARTICULATE SOURCES IN LAGOS, NIGERIA

    African Journals Online (AJOL)

    Elemental concentrations of airborne particulate matter 9 sampled at three urban site classes m Lagos (an industrial city) 1n southWest Nigeria were subjected to statistical -' analysis to determine the number and nature of sources impacting the receptor sites. Inter-elemental Correlation, , '. Principal COmponent Factor ...

  12. Configurationally stable longitudinally twisted polycyclic aromatic compounds.

    Science.gov (United States)

    Walters, Robert S; Kraml, Christina M; Byrne, Neal; Ho, Douglas M; Qin, Qian; Coughlin, Frederick J; Bernhard, Stefan; Pascal, Robert A

    2008-12-03

    Two strategies for the synthesis of configurationally stable twisted polycyclic aromatic compounds (PACs) were pursued. The first approach employed dissymmetrically positioned 1-naphthyl substituents to bias the direction of twist in highly substituted PACs. 2,3-Bis(1-naphthyl)-1,4-diphenyltriphenylene (7) was prepared, and its meso cis-dinaphthyl and enantiomeric trans-dinaphthyl isomers were resolved by preparative supercritical fluid chromatography (SFC) on chiral supports. Similarly, several naphthyl-substituted derivatives of the more highly twisted 9,10,11,12,13,14-hexaphenylbenzo[b]triphenylene (2) were prepared. Of these, 10-(1-naphthyl)-9,11,12,14-tetraphenylbenzo[b]triphenylene (13) was resolved by SFC on a chiral support. The pure enantiomers of trans-7 showed moderately large specific rotations ([alpha]D(25) = -330 and +320 degrees), but the specific rotations for the enantiomers of 13 were unexpectedly small ([alpha]D(25) = -23 and +23 degrees). Computational studies suggest that the latter result is due to presence of a minor conformation of 13 possessing a larger rotation of opposite sign than the major conformation. Both 7 and 13 showed strong circular dichroism and moderately strong circularly polarized luminescence. A byproduct of these syntheses was 9,10,19,21-tetraphenyldiphenanthro[9,10-b:9,10-h]carbazole (15), a very crowded carbazole that exhibits an 81 degree end-to-end twist but is not resolvable. In the second approach, the large, twisted, polycyclic aromatic ligand 9,10,11,12,13,14-hexaphenylbenzo[h]naphtho[2,3-f]quinoline (21, an aza-2) was used to prepare the chiral, cyclometallated iridium(III) complex 4. The ligand 21 was prepared via an unusually stable benzannulated norbornadienone, for which the free energy of activation for decarbonylation was a remarkable 33.5 kcal/mol. The iridium complex 4 proved to be configurationally stable and resolvable by analytical HPLC on chiral supports, but the low solubility of 4 prevented its

  13. The effects of Hurricanes Katrina and Rita on seabed polycyclic aromatic hydrocarbon dynamics in the Gulf of Mexico.

    Science.gov (United States)

    Mitra, Siddhartha; Lalicata, Joseph J; Allison, Mead A; Dellapenna, Timothy M

    2009-06-01

    To assess the extent to which Hurricanes Katrina and Rita affected polycyclic aromatic hydrocarbons (PAH) in the Gulf of Mexico (GOM), sediment cores were analyzed in late 2005 from: a shallow shelf, a deeper shelf, and a marsh station. Sediment geochronology, fabric, and geochemistry show that the 2005 storms deposited approximately 10cm of sediment to the surface of a core at 5-12A. Bulk carbon geochemistry and PAH isomers in this top layer suggest that the source of sediment to the top portion of core 5-12A was from a relatively more marine area. Particulate PAHs in the marsh core (04M) appeared unaffected by the storms while sediments in the core from Station 5-1B (deeper shelf) were affected minimally (some possible storm-derived deposition). Substantial amounts of PAH-laden particles may have been displaced from the seabed in shallow areas of the water column in the GOM by these 2005 storms.

  14. Exposure to genotoxins present in ambient air in Bangkok, Thailand - particle associated polycyclic aromatic hydrocarbons and biomarkers

    DEFF Research Database (Denmark)

    Ruchirawat, Mathuros; Mahidol, Chulabhorn; Tangjarukij, Chanthana

    2002-01-01

    Exposure to genotoxic compounds in ambient air has been studied in Bangkok, Thailand, by analysis of polycyclic aromatic hydrocarbons (PAHs) associated with particles and using different biomarkers of exposure. Eighty-nine male, non-smoking Royal Thai police officers were investigated. The police...... officers were divided into a high exposure group (traffic police) and low exposure (office duty). Particulate matter was collected using personal pumps (2 l/min) and the eight carcinogenic PAHs were analysed by standard procedures. The traffic police was exposed to a 20-fold higher level of total PAHs than...... office police (74.25 ng/m3 vs. 3.11; P= 0.001). A two-fold variation was observed between the different police stations. The major PAHs in all groups was benzo[g,h,l]pyrelene. Large inter-individual differences in biomarker levels were observed, but the level of all markers was statistically...

  15. Concentrations and Sources of Polycyclic Aromatic Hydrocarbons in the Seawater around Langkawi Island, Malaysia

    Directory of Open Access Journals (Sweden)

    Essam Nasher

    2013-01-01

    Full Text Available This paper reports the levels of polycyclic aromatic hydrocarbons (PAHs in the water around the Island and their probable sources. Water samples were collected from four jetties and three marine fish farms around the main Langkawi Island and analysed for 18 polycyclic aromatic hydrocarbons (PAHs in December 2010. The total PAH concentrations ranged from 6.1 ± 0.43 to 46 ± 0.42 μgL−1, which exceed the maximum admissible concentrations of PAHs (0.20 μgL−1 for the water standard of European Union. The calculated diagnostic benzo[a]anthracene : benzo[a]anthracene + chrysene ratio of between 0.52 and 1.0 suggests that the sources of PAHs at the majority of the stations studied are derived primarily from pyrogenic sources, from incomplete fuel combustion of the boats and vehicle engines, with lesser amounts of PAHs contributed from petrogenic sources. Some stations displayed mixed sources. A significant positive correlation was found between total organic carbon (TOC and the concentrations of the high-molecular-weight PAHs (r2=0.86, P<0.05, which suggests significant secondary sources of PAHs, such as those from atmospheric deposition.

  16. Prediction of gas-particle partitioning of polycyclic aromatic hydrocarbons based on M5' model trees

    Directory of Open Access Journals (Sweden)

    Radonić Jelena R.

    2012-01-01

    Full Text Available During the thermal combustion processes of carbon-enriched organic compounds, emission of polycyclic aromatic hydrocarbons into ambient air occurs. Previous studies of atmospheric distribution of polycyclic aromatic hydrocarbons showed low correlation between the experimental values and Junge-Pankow theoretical adsorption model, suggesting that other approaches should be used to describe the partitioning phenomena. The paper evaluates the applicability of multivariate piece-wise-linear M5' model-tree models to the problem of gas-particle partition­ing. Experimental values of particle-associated fraction, obtained for 129 ambient air samples collected at 24 background, urban, and industrial sites, were compared to the prediction results obtained using M5' and the Junge-Pankow model. The M5' approach proposed and models learned are able to achieve good correlation (cor­relation coefficient >0.9 for some low-molecular-weight compounds, when the target is to predict the concentration of gas phase based on the particle-associated phase. When converted to particle-bound fraction values, the results, for selected compounds, are superior to those obtained by Junge-Pankow model by several or­ders of magnitude, in terms of the prediction error.

  17. 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.

  18. 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.

  19. Photoacoustic spectroscopic studies of polycyclic aromatic hydrocarbons

    Science.gov (United States)

    Zaidi, Zahid H.; Kumar, Pardeep; Garg, R. K.

    1999-02-01

    Because of their involvement in environmental pollutants, in carcinogenic activity, plastics, pharmaceuticals, synthesis of some laser dyes and presence in interstellar space etc., Polycyclic aromatic hydrocarbons (PAHs) are important. As their structure and properties can be varied systematically, they form a beautiful class of molecules for experimental and quantum chemical investigations. These molecules are being studied for last several years by using conventional spectroscopy. In recent years, Photoacoustic (PA) spectroscopy has emerged as a new non-destructive technique with unique capability and sensitivity. The PA effect is the process of generation of acoustic waves in a sample resulting from the absorption of photons. This technique not only reveals non- radiative transitions but also provides information about forbidden singlet-triplet transitions which are not observed normally by the conventional spectroscopy. The present paper deals with the spectroscopic studies of some PAH molecules by PA spectroscopy in the region 250 - 400 nm. The CNDO/S-CI method is used to calculate the electronic transitions with the optimized geometries. A good agreement is found between the experimental and calculated results.

  20. Polycyclic aromatic hydrocarbons in the bakery chain.

    Science.gov (United States)

    Ciecierska, M; Obiedziński, M W

    2013-11-01

    The level of polycyclic aromatic hydrocarbons occurrence and the possibility of their formation in the bakery chain, its raw materials and final products, were examined. Experimental bread baking, with different baking temperatures, was performed in the Warsaw bakery, using cyclothermic deck ovens. PAHs determination was performed by high-pressure liquid chromatography with fluorescent and diode array detectors (HPLC-FLD/DAD) and confirmed by gas chromatography coupled with mass spectrometry (GC/MS). Total content of 19 PAHs in the grain, flour and bran varied from 1.07 to 3.65 μg/kg and, in bread, from 1.59 to 13.6 μg/kg depending on the part of bread and baking temperature. Based on the dough's contamination level and the influence of the baking temperature on the bread's PAHs content, it was confirmed that PAHs are formed during baking. Considering the results of the average dietary exposure to PAHs and the MOE (Margin of Exposure) analysis, it could be concluded that analysed bread and cereal products constitute little concern for consumer health. Copyright © 2013 Elsevier Ltd. All rights reserved.

  1. Zirconacyclopentadiene-annulated polycyclic aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Kiel, Gavin R.; Ziegler, Micah S.; Tilley, T. Don [Department of Chemistry, University of California, Berkeley, CA (United States)

    2017-04-18

    Syntheses of large polycyclic aromatic hydrocarbons (PAHs) and graphene nanostructures demand methods that are capable of selectively and efficiently fusing large numbers of aromatic rings, yet such methods remain scarce. Herein, we report a new approach that is based on the quantitative intramolecular reductive cyclization of an oligo(diyne) with a low-valent zirconocene reagent, which gives a PAH with one or more annulated zirconacyclopentadienes (ZrPAHs). The efficiency of this process is demonstrated by a high-yielding fivefold intramolecular coupling to form a helical ZrPAH with 16 fused rings (from a precursor with no fused rings). Several other PAH topologies are also reported. Protodemetalation of the ZrPAHs allowed full characterization (including by X-ray crystallography) of PAHs containing one or more appended dienes with the ortho-quinodimethane (o-QDM) structure, which are usually too reactive for isolation and are potentially valuable for the fusion of additional rings by Diels-Alder reactions. (copyright 2017 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  2. 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.

  3. 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)

  4. 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.

  5. Polycyclic aromatic hydrocarbon emissions from the combustion of alternative fuels in a gas turbine engine.

    Science.gov (United States)

    Christie, Simon; Raper, David; Lee, David S; Williams, Paul I; Rye, Lucas; Blakey, Simon; Wilson, Chris W; Lobo, Prem; Hagen, Donald; Whitefield, Philip D

    2012-06-05

    We report on the particulate-bound polycyclic aromatic hydrocarbons (PAH) in the exhaust of a test-bed gas turbine engine when powered by Jet A-1 aviation fuel and a number of alternative fuels: Sasol fully synthetic jet fuel (FSJF), Shell gas-to-liquid (GTL) kerosene, and Jet A-1/GTL 50:50 blended kerosene. The concentration of PAH compounds in the exhaust emissions vary greatly between fuels. Combustion of FSJF produces the greatest total concentration of PAH compounds while combustion of GTL produces the least. However, when PAHs in the exhaust sample are measured in terms of the regulatory marker compound benzo[a]pyrene, then all of the alternative fuels emit a lower concentration of PAH in comparison to Jet A-1. Emissions from the combustion of Jet A-1/GTL blended kerosene were found to have a disproportionately low concentration of PAHs and appear to inherit a greater proportion of the GTL emission characteristics than would be expected from volume fraction alone. The data imply the presence of a nonlinear relation between fuel blend composition and the emission of PAH compounds. For each of the fuels, the speciation of PAH compounds present in the exhaust emissions were found to be remarkably similar (R(2) = 0.94-0.62), and the results do provide evidence to support the premise that PAH speciation is to some extent indicative of the emission source. In contrast, no correlation was found between the PAH species present in the fuel with those subsequently emitted in the exhaust. The results strongly suggests that local air quality measured in terms of the particulate-bound PAH burden could be significantly improved by the use of GTL kerosene either blended with or in place of Jet A-1 kerosene.

  6. Determination of polycyclic aromatic hydrocarbons in coal combustion gas using high performance liquid chromatography

    Energy Technology Data Exchange (ETDEWEB)

    Katoh, N. [Ishikawajima Harima Heavy Industry Co Ltd, Tokyo (Japan). Research Institution

    2002-11-01

    The study describes a sampling and analysis procedure for polycyclic aromatic hydrocarbons (PAH) at high temperatures in flue gas. Particulate matter sampling was used in conjunction with gas phase sampling. Particulates were collected on quartz fiber filter heated at the same temperature as flue gas. Vaporous PAHs not retained by the filter were cooled at 55{sup o}C and trapped from the gas phase on Tenax-GC polymer beads of 10 g. The sample volume was about 1 m{sup 3}. Tenax-GC has demonstrated high collection efficiency for benzo(a)pyrene (B(a)P) generated at 375{sup o}C under a stream of nitrogen. PAH were extracted with n-pentane for 4 h by a continuous PAH extractor. It demonstrated 99% extraction efficiency for B(a)P spiked on the adsorbent and it was more effective than Soxhlet extraction. The extracts were concentrated to 1 ml of n-pentane in a Kuderna Danish evaporator. Qualitative and quantitative analysis of the extracts were performed by high performance liquid chromatograph (HPLC) with ultraviolet/fluorescence detection. Eight PAH (3,4,5,6-dibenzocarbazole, phenanthrene, anthracene, fluoranthene, pyrene, 2-methylanthracene, benz(a)anthracene, benzo(a)pyrene) were determined in coal combustion gas on reducing NOx procedures. It was demonstrated that the tendency to reduce NOx levels leads to an increase in the PAH present. Moreover total concentration of four PAH (phenanthrene, fluoranthene, pyrene, benzo(a)pyrene) in this study is satisfactory agreement with those measured in the emissions of coal-fired power stations in the literature.

  7. Protective coatings for commercial particulates

    DEFF Research Database (Denmark)

    Kindl, B.; Teng, Y.H.; Liu, Y.L.

    1994-01-01

    SiC/Al composites are in large-scale production with Al-Si alloy matrices. The same composites with pure Al or low Si matrices need diffusion barriers on the SiC reinforcement to control the interfacial reaction. The present paper describes various approaches taken to obtain protective coatings...... of alumina and zirconia on SiC particulates by sol-gel techniques. Aqueous and organic precursors have been used. The extent of the reaction, i.e., the Si and Al4C3 content in the matrix, was determined by differential thermal analysis and X-ray diffraction. The reaction rates of some coated particulates...... in liquid Al are decreased by as much as one order of magnitude during the first 15 min of immersion. Pretreatments of the SiC surface, the composition and thickness of the coating interphase and heat treatments of the coated materials have been studied, and are discussed in relation to their effect...

  8. SOUTHERN FINE PARTICULATE MONITORING PROJECT

    Energy Technology Data Exchange (ETDEWEB)

    Ashley D. Williamson

    2002-01-31

    This quarterly report presents results and analysis of continuous onsite ambient fine particulate data at the North Birmingham sampling site during the October--December, 2001 study period. The continuous data include PM{sub 2.5} mass concentrations measured by TEOM, particle sulfate using the R&P 8400S monitor, particle size distributions measured by SMPS and APS monitors, and PM{sub 2.5} light scattering extinction coefficient as measured by nephelometer. The persistent daily trends described in the previous quarterly report are seen in the fall particulate data, superimposed on the seasonal trend toward lower concentrations in the cooler months. Some instrumental issues were noted with the APS and the sulfate monitoring instruments, as described in the main report.

  9. Atmospheric Dispositifs

    DEFF Research Database (Denmark)

    Wieczorek, Izabela

    2015-01-01

    Through the coupling of dispositif with atmosphere this paper engages in a discussion of the atmospherics as both a form of knowledge and a material practice. In doing so the objective is to provide an inventory of tools and methodologies deployed in the construction of atmosphere understood......, the conceptual foundations and protocols for the production of atmosphere in architecture might be found beneath the surface of contemporary debates. In this context, the notion of atmospheric dispositif – illustrated through an oeuvre of the German architect Werner Ruhnau and its theoretical and historical...

  10. SOUTHERN FINE PARTICULATE MONITORING PROJECT

    Energy Technology Data Exchange (ETDEWEB)

    Ashley D. Williamson

    2001-07-01

    This is the third quarterly progress report of the ''Southern Fine Particulate Monitoring Project'', funded by the U.S. Department of Energy's National Energy Technology Laboratory under DOE Cooperative Agreement No. DE-FC26-00NT40770 to Southern Research Institute (SRI). In this two year project SRI will conduct detailed studies of ambient fine particulate matter in the Birmingham, AL metropolitan area. Project objectives include: Augment existing measurements of primary and secondary aerosols at an established urban southeastern monitoring site; Make a detailed database of near-continuous measurements of the time variation of fine particulate mass, composition, and key properties (including particle size distribution); Apply the measurements to source attribution, time/transport properties of fine PM, and implications for management strategies for PM{sub 2.5}; and Validate and compare key measurement methods used in this study for applicability within other PM{sub 2.5} research by DOE-FE, EPA, NARSTO, and others. During the third project quarter, the new SRI air monitoring shelter and additional instruments were installed at the site. Details include: Installation of Radiance Research M903 Nephelometer; Installation of SRI air monitoring shelter at North Birmingham Site; Relocation of instruments from SEARCH shelter to SRI shelter; Installation of Rupprecht & Patashnick 8400 Sulfate Monitor; Assembly and initial laboratory testing for particulate sulfate monitor of Harvard design; Efficiency testing of particle sizing instrument package at SRI lab; Preparation for the Eastern Supersite July measurement intensive program; and Continued monitoring with TEOM and particle sizing instruments.

  11. Material Instabilities in Particulate Systems

    Science.gov (United States)

    Goddard, J. D.

    1999-01-01

    Following is a brief summary of a theoretical investigation of material (or constitutive) instability associated with shear induced particle migration in dense particulate suspensions or granular media. It is shown that one can obtain a fairly general linear-stability analysis, including the effects of shear-induced anisotropy in the base flow as well as Reynolds dilatancy. A criterion is presented here for simple shearing instability in the absence of inertia and dilatancy.

  12. 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.

  13. Polycyclic aromatic hydrocarbon-DNA adducts in Beluga whales from the Arctic

    Energy Technology Data Exchange (ETDEWEB)

    Mathieu, A.; Payne, J.F.; Fancey, L.L. [Department of Fisheries and Oceans, St. John`s Newfoundland (Canada)] [and others

    1997-09-01

    The Arctic is still relatively pristine in nature, but it is also vulnerable to pollution because contaminants originating from midlatitudes are transported to the Arctic by atmospheric processes, ocean currents, and river. Recognition of this fact of Arctic vulnerability has resulted in a Declaration on the Protection of the Arctic Environment by eight Arctic countries. A manifest aim of this declaration is to develop an Arctic Monitoring and Assessment Program. We report here on the presence of measurable levels of polycyclic aromatic hydrocarbon-DNA adducts, including relatively high levels in Arctic beluga (Delphinapterus leucas). These results lend support to the value of developing biological assessment programs for Arctic wildlife. 15 refs., 1 tab.

  14. A review of airborne polycyclic aromatic hydrocarbons (PAHs) and their human health effects.

    Science.gov (United States)

    Kim, Ki-Hyun; Jahan, Shamin Ara; Kabir, Ehsanul; Brown, Richard J C

    2013-10-01

    Polycyclic aromatic hydrocarbons (PAHs) are a large group of organic compounds comprised of two or more fused benzene rings arranged in various configurations. PAHs are widespread environmental contaminants formed as a result of incomplete combustion of organic materials such as fossil fuels. The occurrence of PAHs in ambient air is an increasing concern because of their carcinogenicity and mutagenicity. Although emissions and allowable concentrations of PAHs in air are now regulated, the health risk posed by PAH exposure suggests a continuing need for their control through air quality management. In light of the environmental significance of PAH exposure, this review offers an overview of PAH properties, fates, transformations, human exposure, and health effects (acute and chronic) associated with their emission to the atmosphere. Biomarkers of PAH exposure and their significance are also discussed. © 2013.

  15. SOUTHERN FINE PARTICULATE MONITORING PROJECT

    Energy Technology Data Exchange (ETDEWEB)

    Ashley D. Williamson

    2001-04-01

    This is the second quarterly progress report of the ''Southern Fine Particulate Monitoring Project'', funded by the U.S. Department of Energy's National Energy Technology Laboratory under DOE Cooperative Agreement No. DE-FC26-00NT40770 to Southern Research Institute (SRI). In this two year project SRI will conduct detailed studies of ambient fine particulate matter in the Birmingham, AL metropolitan area. Project objectives include: Augment existing measurements of primary and secondary aerosols at an established urban southeastern monitoring site; Make a detailed database of near-continuous measurements of the time variation of fine particulate mass, composition, and key properties (including particle size distribution); Apply the measurements to source attribution, time/transport properties of fine PM, and implications for management strategies for PM{sub 2.5}; and Validate and compare key measurement methods used in this study for applicability within other PM{sub 2.5} research by DOE-FE, EPA, NARSTO, and others.

  16. 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'' is...

  17. 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)

  18. Atmospheric Chemistry of Micrometeoritic Organic Compounds

    Science.gov (United States)

    Kress, M. E.; Belle, C. L.; Pevyhouse, A. R.; Iraci, L. T.

    2011-01-01

    Micrometeorites approx.100 m in diameter deliver most of the Earth s annual accumulation of extraterrestrial material. These small particles are so strongly heated upon atmospheric entry that most of their volatile content is vaporized. Here we present preliminary results from two sets of experiments to investigate the fate of the organic fraction of micrometeorites. In the first set of experiments, 300 m particles of a CM carbonaceous chondrite were subject to flash pyrolysis, simulating atmospheric entry. In addition to CO and CO2, many organic compounds were released, including functionalized benzenes, hydrocarbons, and small polycyclic aromatic hydrocarbons. In the second set of experiments, we subjected two of these compounds to conditions that simulate the heterogeneous chemistry of Earth s upper atmosphere. We find evidence that meteor-derived compounds can follow reaction pathways leading to the formation of more complex organic compounds.

  19. 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

  20. Emissions of polycyclic aromatic hydrocarbons from thermal pre-treatment of waste hydrodesulfurization catalysts.

    Science.gov (United States)

    Lai, Yi-Chieh; Lee, Wen-Jhy; Huang, Kuo-Lin; Huang, Hong-Hsin

    2007-09-01

    Despite increasing environmental concerns and stringent limitations on the sulfur content in fuels, many waste hydrodesulfurization (HDS) catalysts containing Co, Mo, Ni and V are generated in the petroleum refining process. To recover valuable metals in the waste HDS catalysts via hydrometallurgy, thermal treatment is usually performed first to remove contaminants (residual oil, carbon and sulfur) present on the surface of catalysts. In this study, the mass partitions of polycyclic aromatic hydrocarbons (PAHs) in different media (aqueous, particulate and gaseous) were quantified in order to determine the efficiency of three different air pollution control devices, cooling unit, filter and glass cartridge, on PAH removal. An afterburner and two furnace temperatures were used to observe the effect on the PAH contents of the treated residues. Results show that total-PAH content in treated residues decreased with the pyrolysis temperature of the primary furnace, while those generated in flue gases were destroyed by the afterburner at an efficiency of approximately 95%. In addition, the thermal process converts high molecular weight PAHs to low molecular weight PAHs, and the afterburner temperature involved (1200 degrees C) was high enough to prohibit the generation of high molecular weight PAHs (HM-PAHs), leading to the domination of low molecular weight PAHs (LM-PAHs) in flue gases, while treated residues were dominated by HM-PAHs. Finally, information on metal contents and their concentrations in the Toxicity Characteristic Leaching Procedure in waste HDS catalyst and thermal treated residues are examined as an index of the potential for metal recovery.

  1. Predictors of polycyclic aromatic hydrocarbon exposure and internal dose in inner city Baltimore children.

    Science.gov (United States)

    Peters, Kamau O; Williams, D' Ann L; Abubaker, Salahadin; Curtin-Brosnan, Jean; McCormack, Meredith C; Peng, Roger; Breysse, Patrick N; Matsui, Elizabeth C; Hansel, Nadia N; Diette, Gregory B; Strickland, Paul T

    2017-05-01

    Polycyclic aromatic hydrocarbons (PAHs), the by-products of incomplete combustion of organic materials, are commonly found on particulate matter (PM) and have been associated with the development of asthma and asthma exacerbation in urban populations. We examined time spent in the home and outdoors as predictors of exposures to airborne PAHs and measured urinary 1-hydroxypyrene-glucuronide (1-OHPG) as internal dose of PAHs in 118 children aged 5-12 years from Baltimore, MD. During weeklong periods (Saturday-Saturday) in each of four seasons: daily activities were assessed using questionnaires, indoor air nicotine and PM concentrations were monitored, and urine specimens were collected on Tuesday (day 3) and Saturday (day 7) for measurement of 1-OHPG. Time spent in non-smoking homes was associated with significantly decreased 1-OHPG concentration in urine (β=-0.045, 95% CI (-0.076, -0.013)), and secondhand smoke (SHS) exposures modified these associations, with higher urinary 1-OHPG concentrations in children spending time in smoking homes than non-smoking homes (P-value for interaction=0.012). Time spent outdoors was associated with increased urinary 1-OHPG concentrations (β=0.097, 95% CI (0.037, 0.157)) in boys only. Our results suggest that SHS and ambient (outdoor) air pollution contribute to internal dose of PAHs in inner city children.

  2. Quantitative Analysis of Polycyclic Aromatic Hydrocarbons (PAHs Cited by the United States Food and Drug Administration

    Directory of Open Access Journals (Sweden)

    Guthery W

    2014-12-01

    Full Text Available The yields of 16 polycyclic aromatic hydrocarbons (PAHs were determined from cigarette mainstream smoke condensate extracts using Gas Chromatography- Tandem Mass Spectrometry (GC-MS/MS. The method has been validated for ISO and Health Canada Intense (HCI smoking protocols. Quantifiable levels (ISO means 0.16 to 365 ng/cig; HCI means 0.33 to 1595 ng/cig; n = 30 of 15 PAHs were found in the Kentucky reference cigarette K3R4F. The coefficient of variance (CV was derived from ten determinations each run in triplicate. The CV range was 8.7% to 24.8% (ISO and 6.6% to 24.3% (HCI. The limit of detection (LOD based on empirical precision was ≤ 0.06 ng/cig (ISO and ≤ 0.20 ng/cig (HCI for all components except naphthalene (2.89 and 9.62 ng/cig, respectively. The yields from 5 unspecified branded cigarettes (Samples A-E and 2 other reference cigarettes, K1R5F and the CORESTA monitor CM7, were determined under ISO smoking conditions. The same 15 PAHs were detected as in the K3R4F; however, cigarettes with lower yields of total particulate matter (TPM were found to contain significantly less PAHs. One component was measured below the limit of quantification (LOQ in Sample E and 2 components were < LOQ in the K1R5F.

  3. Source apportionment of chlorinated polycyclic aromatic hydrocarbons associated with ambient particles in a Japanese megacity

    Science.gov (United States)

    Kamiya, Yuta; Iijima, Akihiro; Ikemori, Fumikazu; Okuda, Tomoaki; Ohura, Takeshi

    2016-12-01

    Chlorinated polycyclic aromatic hydrocarbons (ClPAHs) are novel species of environmental contaminants whose possible sources remain unclear. The occurrence of ClPAHs within total suspended particles (TSP) is compared with weekly air samples at two sites of differing characteristics (industrial and residential) in the megacity of Nagoya, Japan. Samples were collected over 12 months during 2011-2012. All 24 species of targeted ClPAHs were detected at both industrial and residential sites, where mean concentrations of total ClPAHs in TSP were 20.7 and 14.1 pg/m3, respectively. High concentrations at the industrial site were frequently observed during winter, suggesting potent seasonal ClPAH sources there. Positive matrix factorization modeling of particulate ClPAH source identification and apportioning were conducted for datasets including ClPAHs, PAHs, elements and ions, plus elemental carbons in TSP. Eight factors were identified as possible ClPAH sources, with estimates that the dominant one was a specific source of ClPAH emission (31%), followed by traffic (23%), photodegradable and semi-volatile species (18%), long-range transport (11%), and industry and oil combustion (10%). Source contributions of ClPAHs differed substantially from those of PAHs. This suggests specific and/or potent ClPAH sources in the local area, and that the production mechanisms between ClPAHs and PAHs are substantially different.

  4. Polycyclic aromatic hydrocarbons (PAHs) in burning and non-burning coal waste piles.

    Science.gov (United States)

    Ribeiro, Joana; Silva, Tais; Mendonca Filho, Joao Graciano; Flores, Deolinda

    2012-01-15

    The coal waste material that results from Douro Coalfield exploitation was analyzed by gas chromatography with mass spectrometry (GC-MS) for the identification and quantification of the 16 polycyclic aromatic hydrocarbons (PAHs), defined as priority pollutants. It is expected that the organic fraction of the coal waste material contains PAHs from petrogenic origin, and also from pyrolytic origin in burning coal waste piles. The results demonstrate some similarity in the studied samples, being phenanthrene the most abundant PAH followed by fluoranthene and pyrene. A petrogenic contribution of PAHs in unburned samples and a mixture of PAHs from petrogenic and pyrolytic sources in the burning/burnt samples were identified. The lowest values of the sum of the 16 priority PAHs found in burning/burnt samples and the depletion LMW PAHs and greater abundance of HMW PAHs from the unburned coal waste material relatively to the burning/burnt material demonstrate the thermal transformation attributed to the burning process. The potential environmental impact associated with the coal waste piles are related with the release of petrogenic and pyrolytic PAHs in particulate and gaseous forms to soils, sediments, groundwater, surface water, and biodiversity. Copyright © 2011 Elsevier B.V. All rights reserved.

  5. 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...

  6. Exposure of iron foundry workers to polycyclic aromatic hydrocarbons

    DEFF Research Database (Denmark)

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

    1994-01-01

    Exposure to polycyclic aromatic hydrocarbons (PAHs) in foundry workers has been evaluated by determination of benzo(a)pyrene-serum albumin adducts and urinary 1-hydroxypyrene. Benzo(a)pyrene binding to albumin and 1-hydroxypyrene were quantitatively measured by enzyme linked immunosorbent assay...... 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...

  7. 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.

  8. Evaluation of principal cannabinoids in airborne particulates.

    Science.gov (United States)

    Balducci, C; Nervegna, G; Cecinato, A

    2009-05-08

    The determination of delta(9)-tetrahydrocannabinol (Delta9-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.

  9. Ozone removal by diesel particulate matter

    Science.gov (United States)

    Metts, T. A.; Batterman, S. A.; Fernandes, G. I.; Kalliokoski, P.

    The most significant removal mechanisms for tropospheric ozone (O 3) include dry deposition, photolysis, and photochemical reactions. This study examines another mechanism potentially important in urban areas: sorption and removal on diesel particulate matter (DPM). Tests were performed to determine O 3 breakthrough and the amount of O 3 removed by the DPM generated by a heavy-duty diesel engine. Teflon filters loaded with 0.7-1.8 mg of DPM were exposed to a test atmosphere of humidified and ozonated air designed to represent realistic ambient air conditions. In addition, soot samples with the organic fraction removed were tested to determine whether the organic or elemental fraction contributed to O 3 removal. For comparison, activated carbon (AC) samples were also tested. The DPM-loaded filters removed 5.6±1.8 wt% of O 3. Considerably more ozone, 31±4 wt %, was removed by the DPM after removal of its soluble organic fraction. Removal capacities of DPM were small relative to AC, which removed >38±3 wt% of O 3. Of the Lagergren pseudo-first-order, pseudo-second-order, Elovich, and Ritchie chemisorption models tested, the Ritchie model provided the best fit to the breakthrough data. Preliminary estimates drawn from laboratory results suggest that diesel soot present at typical urban levels will remove only a small portion of O 3 from urban or tropospheric air. In air cleaning applications, DPM-loaded filters are also expected to remove only a small portion of indoor O 3.

  10. Articulating Atmospheres

    DEFF Research Database (Denmark)

    Kinch, Sofie

    2011-01-01

    This paper presents an architectural approach to designing computational interfaces by articulating the notion of atmosphere in the field of interaction design. It draws upon the concept of kinesthetic interaction and a philosophical notion on atmosphere emphasizing the importance of bodily exper......” implications and qualities of the approach are identified through concrete examples of a design case, which also investigates the qualities and implications of addressing atmospheres both as design concern and user experience.......This paper presents an architectural approach to designing computational interfaces by articulating the notion of atmosphere in the field of interaction design. It draws upon the concept of kinesthetic interaction and a philosophical notion on atmosphere emphasizing the importance of bodily...... experience in space, presented as middle ground experience. In the field of HCI, middle ground experiences complete the unarticulated spectrum between designing for foreground of attention or background awareness. When “Articulating Atmospheres through Middle Ground Experiences in Interaction Design...

  11. Anthropogenic and Dust Particulate During Ace-asia

    Science.gov (United States)

    Coe, H.; Alfarra, M. R.; Allan, J. D.; Berner, A.; Bower, K. N.; Choularton, T. W.; Facchini, M. C.; Fuzzi, S.; Galllagher, M. W.; McFiggans, G.; Topping, D.; Williams, P. I.

    Measurements of aerosol microphysics and chemical composition have been made on the island of Cheju-Do, Korea during the ACE-ASIA project throughout April 2001. The overall aim of ACE-ASIA was to understand the interaction between dust particles, emitted into the atmosphere during storms over the dry Asian continent, with anthropogenic pollution produced extensively around the coastal regions of the Yellow Sea. The lowest few kilometres of the troposphere are heavily laden with particulate for much of the time in this region and this has a significant impact on the radiative budget in this part of the world. In this paper we discuss the interaction between these two major sources of particulate matter using measurements of aerosol number, size distribution, online chemical composition as a function of size and impactor samples, analysed for water soluble organic compounds in addition to the standard analyses of inorganic species. We show the difference in composition between particulate emitted from various pollution source regions and the extent to which these sources modify the dust particles. Lastly we discuss the likely sources of inorganic material, in particular the high levels of nitrate, present in the dust aerosol measured at Cheju-Do.

  12. Atmospheric pollution in thermal power plants; Contaminacion atmosferica en centrales termicas convencionales

    Energy Technology Data Exchange (ETDEWEB)

    Aguirre Diaz, A.

    1997-04-01

    The author presents the atmospheric pollution by fossil-fuel power plants. The state of the art is developed in 4 chapters: Legislation, Sulfur dioxide: reduction of SO{sub 2}, nitrogen oxides: reduction of emissions, particulates: reduction of particulates and new technologies. (Author)

  13. 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").

  14. Atmospheric electricity

    CERN Document Server

    Chalmers, J Alan

    1957-01-01

    Atmospheric Electricity brings together numerous studies on various aspects of atmospheric electricity. This book is composed of 13 chapters that cover the main problems in the field, including the maintenance of the negative charge on the earth and the origin of the charges in thunderstorms. After a brief overview of the historical developments of atmospheric electricity, this book goes on dealing with the general principles, results, methods, and the MKS system of the field. The succeeding chapters are devoted to some aspects of electricity in the atmosphere, such as the occurrence and d

  15. Atmospheric Neutrinos

    Directory of Open Access Journals (Sweden)

    Takaaki Kajita

    2012-01-01

    Full Text Available Atmospheric neutrinos are produced as decay products in hadronic showers resulting from collisions of cosmic rays with nuclei in the atmosphere. Electron-neutrinos and muon-neutrinos are produced mainly by the decay chain of charged pions to muons to electrons. Atmospheric neutrino experiments observed zenith angle and energy-dependent deficit of muon-neutrino events. It was found that neutrino oscillations between muon-neutrinos and tau-neutrinos explain these data well. This paper discusses atmospheric neutrino experiments and the neutrino oscillation studies with these neutrinos.

  16. Diesel particulate filter with zoned resistive heater

    Science.gov (United States)

    Gonze, Eugene V [Pinckney, MI

    2011-03-08

    A diesel particulate filter assembly comprises a diesel particulate filter (DPF) and a heater assembly. The DPF filters a particulate from exhaust produced by an engine. The heater assembly has a first metallic layer that is applied to the DPF, a resistive layer that is applied to the first metallic layer, and a second metallic layer that is applied to the resistive layer. The second metallic layer is etched to form a plurality of zones.

  17. SIMULATION MODEL FOR FLOWAGE OF PARTICULATE MATERIAL

    OpenAIRE

    Ryosuke, KITAMURA; Seisaku, FUKUHARA; George, KISANUKI; Professor, Dept. of Ocean Civil Engineering, Kagoshima University; Technical Clerk, Kagoshima Prefecture (formerly Graduate Student, Kagoshima Univ.); Graduate Student, Kagoshima University

    1995-01-01

    A new slope stability analysis method based on consideration of particle scale is proposed for the analysis of the flowage of particulate material, in which the equilibrium condition of the particulate material is examined on the basis of the inter-particle force at a contact point caused by surface tension. The decrease in inter-particle force is considered as one of the main factors for the flowage of particulate material and corresponds to the slope failure. Several numerical experiments h...

  18. Polycyclic aromatic hydrocarbons in soils around Guanting Reservoir, Beijing, China

    NARCIS (Netherlands)

    Jiao, W.T.; Lu, Y.L.; Wang, T.Y.; Li, J.; Han, Jingyi; Wang, G.; Hu, W.Y.

    2009-01-01

    The concentrations of 16 polycyclic aromatic hydrocarbons ( 16PAHs) were measured by gas chromatography equipped with a mass spectrometry detector (GC-MS) in 56 topsoil samples around Guanting Reservior (GTR), which is an important water source for Beijing. Low to medium levels of PAH contamination

  19. Determination of levels of polycyclic aromatic hydrocarbons in soil ...

    African Journals Online (AJOL)

    MICHAEL HORSFALL

    ABSTRACT: Soil samples contaminated with spent motor engine oil collected from Abakaliki auto-mechanic site were analyzed to determine the concentration of polycyclic aromatic hydrocarbon (PAH) components which are often targets in environmental check. Identification and quantification of the PAH components was ...

  20. Polycyclic aromatic hydrocarbons as a tracer of star formation?

    NARCIS (Netherlands)

    Peeters, E; Spoon, HWW; Tielens, AGGM

    2004-01-01

    Infrared (IR) emission features at 3.3, 6.2, 7.7, 8.6, and 11.3 mum are generally attributed to IR fluorescence from ( mainly) far-ultraviolet (FUV) pumped large polycyclic aromatic hydrocarbon (PAH) molecules. As such, these features trace the FUV stellar flux and are thus a measure of star

  1. Polycyclic aromatic hydrocarbons in water, sediment and fish from ...

    African Journals Online (AJOL)

    The Warri River at Ubeji, Nigeria, receives pollutants from an oil refinery. The levels of 16 priority polycyclic aromatic hydrocarbons (PAHs) in water, sediment and the tissue of tilapia from the Warri River were investigated in 2010 using gas chromatography with mass spectrometry. Eleven PAHs were found in the sediment ...

  2. Growth study on chrysene degraders isolated from polycyclic ...

    African Journals Online (AJOL)

    GRACE

    2006-05-16

    May 16, 2006 ... Acinetobacter anitratus, Alcaligenes faecalis, Acinetobacter mallei and Micrococcus varians were isolated from polycyclic aromatic hydrocarbon polluted soils by enrichment culture using chrysene as sole carbon and energy source. Physiochemical evaluation revealed that these isolates grew well at a.

  3. Polycyclic aromatic hydrocarbons and fatal ischemic heart disease.

    NARCIS (Netherlands)

    Burstyn, I.; Kromhout, H.; Partanen, T.A.; Svane, O.; Langard, S.; Ahrens, W.; Kauppinen, T.; Stucker, I.; Shaham, J.; Heederik, D.; Ferro, G.; Heikkila, P.; Hooiveld, M.; Johansen, C.; Randem, B.G.; Boffetta, P.

    2005-01-01

    BACKGROUND: Several toxicologic and epidemiologic studies have produced evidence that occupational exposure to polycyclic aromatic hydrocarbons (PAH) is a risk factor for ischemic heart disease (IHD). However, a clear exposure-response relation has not been demonstrated. METHODS: We studied a

  4. Polycyclic aromatic hydrocarbons in municipal waste ashes from ...

    African Journals Online (AJOL)

    The levels of isolated polycyclic aromatic hydrocarbons (PAH) in ash residues of wastes from some major waste dumps in Lagos, Nigeria, were determined. The total amounts of the PAH in the ashes were in the range of 0.06 – 0.4 mg/g. The ash from the waste dump that contains the highest level also displayed greatest ...

  5. Growth study on chrysene degraders isolated from polycyclic ...

    African Journals Online (AJOL)

    Acinetobacter anitratus, Alcaligenes faecalis, Acinetobacter mallei and Micrococcus varians were isolated from polycyclic aromatic hydrocarbon polluted soils by enrichment culture using chrysene as sole carbon and energy source. Physiochemical evaluation revealed that these isolates grew well at a temperature range of ...

  6. carcinogenic potency of polycyclic aromatic hydrocarbons in soil

    African Journals Online (AJOL)

    Carcinogenic potency of polycyclic aromatic hydrocarbons (PAHs) in soils obtained from seven different sampling locations in Effurun metropolis and its environs of Niger Delta Area of Nigeria were evaluated. The 16 US EPA priority PAHs were determined with GC-MS. The concentrations of individual PAHs observed were ...

  7. Polycyclic aromatic hydrocarbons in air samples of meat smokehouses

    DEFF Research Database (Denmark)

    Hansen, Åse Marie; Olsen, I L; Poulsen, O M

    1992-01-01

    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...

  8. Environmental polycyclic aromatic hydrocarbons affect androgen receptor activation in vitro

    DEFF Research Database (Denmark)

    Vinggaard, Anne Marie; Hnida, Christina; Larsen, John Christian

    2000-01-01

    Nine structurally different polycyclic aromatic hydrocarbons (PAHs) were tested for their ability to either agonize or antagonize the human androgen receptor (hAR) in a sensitive reporter gene assay based on CHO cells transiently cotransfected with a hAR vector and an MMTV-LUC vector. Benz...

  9. Polycyclic aromatic hydrocarbons (PAH) in Danish barbecued meat

    DEFF Research Database (Denmark)

    Duedahl-Olesen, Lene; Aaslyng, Margit Dall; Meinert, Lene

    2015-01-01

    Barbecuing is known to result in the formation of polycyclic aromatic hydrocarbons (PAHs). A validated method that employed pressurized liquid extraction (PLE), gel permeation chromatography (GPC) followed by solid phase extraction (SPE) on Silica and analytical determination by GC-MS was applied...

  10. The polycyclic Lausche Volcano (Lausitz Volcanic Field) and its message\

    Czech Academy of Sciences Publication Activity Database

    Wenger, E.; Büchner, J.; Tietz, O.; Mrlina, Jan

    2017-01-01

    Roč. 292, September (2017), s. 193-210 ISSN 0169-555X Institutional support: RVO:67985530 Keywords : Lausche * polycyclic volcanism * Lausitz Overthrust (Lusatian Fault) * North Bohemian-Saxonian Cretaceous Basin Subject RIV: DC - Siesmology, Volcanology, Earth Structure Impact factor: 2.958, year: 2016

  11. Distribution of Polycyclic Aromatic Hydrocarbons (PAHs) in a tropical ...

    African Journals Online (AJOL)

    The distribution of 8 polycyclic aromatic hydrocarbons (PAHs) in the surface sediments of the Grand-Lahou lagoon (Côte d'Ivoire) was investigated using a high performance liquid chromatography (HPLC). The total concentrations of PAHs were between 1.55 and 437.52 μg/g in the dry season. Pyrene, benzo (b) ...

  12. An Evaluation of Polycyclic Aromatic Hydrocarbons in Hemichromis ...

    African Journals Online (AJOL)

    The concentrations of Polycyclic Aromatic Hydrocarbons (PAHs) were analysed in Hemichromis fasciatus netted from the Ikpoba reservoir in Benin City, Nigeria, using Gas chromatographic technique, in order to evaluate the potential ecological risk of these organic pollutants on the investigated ecosystem. The mean ...

  13. Biodegradation of polycyclic aromatic hydrocarbons in crude oil ...

    African Journals Online (AJOL)

    Release of crude oil and its products into the environment has resulted in many problems that are of global concern. The objective of this study was to determine effect of Composted Market Waste (CMW) on the degradation of Polycyclic Aromatic Hydrocarbons (PAHs) in crude oil-contaminated soil. Pot experiment was ...

  14. A study of the microbiology and polycyclic aromatic hydrocarbons ...

    African Journals Online (AJOL)

    A study was carried out on the drill cuttings from three different oil and gas wells located at Ologbo Community at Edo State with respect to their microbiology and polycyclic aromatic hydrocarbons (PAHs) compositional profile and sources. Isolation and enumeration of heterotrophic bacteria and fungi was carried out using ...

  15. Biodegradation of Polycyclic Aromatic Hydrocarbons in Crude oil ...

    African Journals Online (AJOL)

    ADOWIE PERE

    ABSTRACT: Release of crude oil and its products into the environment has resulted in many problems that are of global concern. The objective of this study was to determine effect of Composted Market Waste (CMW) on the degradation of Polycyclic Aromatic Hydrocarbons (PAHs) in crude oil-contaminated soil.

  16. SHPOLSKII SPECTROFLUORIMETRIC DETERMINATION OF POLYCYCLIC AROMATIC-HYDROCARBONS IN BIOTA

    NARCIS (Netherlands)

    ARIESE, F; GOOIJER, C; Velthorst, N.H.; Hofstraat, J.W.

    1990-01-01

    The applicability of high-resolution Shpol'skii spectrofluorimetry to the direct analysis of polycyclic aromatic hydrocarbons (PAHs) in tern and mussel samples was investigated. The sensitivity of the measurements suffered considerably from the large amounts of interfering (e.g., fatty components)

  17. Potential for biodegradation of polycyclic aromatic hydrocarbons by ...

    African Journals Online (AJOL)

    WiTT

    2012-05-08

    May 8, 2012 ... mutagenic polycyclic aromatic hydrocarbons (PAHs) that accumulate steadily with mileage because of direct leakage of fuel into the motor oil as well as the accumulation of incomplete combustion products (Keith and Telliard, 1979; Grimmer et al., 1981; Pruell and. Quinn, 1988; Hagwell et al., 1992; ...

  18. Monofluorinated polycyclic aromatic hydrocarbons in Shpol'skii spectroscopy

    NARCIS (Netherlands)

    luthe, G.; Scharp, J.; Brinkman, U.A.T.; Gooijer, C.

    2001-01-01

    The basic requirement to achieve high resolution in Shpol'skii spectroscopy is that the guest molecules fit well in the crystalline host alkane matrix, a condition that is usually met by polycyclic aromatic hydrocarbons (PAHs). Despite the electronegativity of the fluorine atom, which might be

  19. 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. Particulates were present in 63 and 80% of fish hearts and 70 and 89% of stomach muscularis collected in 2011 and 2012, respectively. Tissue embedded particulates can lead to localized cellular damage from bioavailable compounds, as well as chronic effects from occlusion of sensitive tissues' blood flow. The PAH derived particulates appeared to act as emboli in small capillaries, and could associated with localized inflammation, focal necrosis and inappropriate collagen and fibroblast tissue repair. We believe large volume filter feeding teleosts, such as menhaden (up to 3 million gallons per year/fish) with high lipid content, have a higher exposure risk and greater potential for toxicity from toxic particulates than other higher trophic level finfish. Suspended PAH derived particulates following an oil spill therefore, should be considered when assessing long-term ecological impacts and not be limited to physical contact (coating) or water soluble fractions for assessing toxicity (gill and neurologic).

  20. Natural, anthropogenic and fossil organic matter in river sediments and suspended particulate matter: a multi-molecular marker approach.

    Science.gov (United States)

    Micić, V; Kruge, M A; Köster, J; Hofmann, T

    2011-02-01

    Different classes of organic matter (OM) have been systematically investigated in sediments and suspended particulate matter (SPM) along the Danube River in order to understand causes of compositional changes. Analytical pyrolysis revealed the dominance of natural organic matter (NOM) in most of the samples. The predominance of aquatic biomass is evident mainly from the abundance of organonitrogen compounds and phenol distributions. As the river enters a forested gorge, the terrestrial component of the NOM in sediments is more significant. This is reflected in abundant methoxyphenols and a very high carbon preference index. SPM sample from a tributary shows a unique geochemical signature. It contains abundant carboxylic acids, amines, isoprenoids in the pyrolyzate, and is dominated by phytol and 24-methyl-cholesta-5,24(28)-dien-3β-ol in the extract, produced by a diatom bloom. Wax esters with a relatively high proportion of short, methyl-branched alkyl-chains appear together with abundant phytadienes and n-C(17) alkane in some samples, suggesting a microbial origin. Anthropogenic OM from runoff and atmospheric deposition was evident from a minor input of polycyclic aromatic hydrocarbons (PAHs) originating from mixed combustion sources. Multivariate analysis using PAH data led us to define simple molecular ratios to distinguish the PAH composition in sand and silty sediments. The newly defined ratios are the alkylated phenanthrenes and anthracenes ratio (APA; C(1)-C(3)/C(0)-C(3) phenanthrenes and anthracenes) and the PAH ring number ratio (RN; 5-6 ring parent PAHs/all parent PAHs). This demonstrates that alkylated, as well as 5-6 ring PAHs are better preserved in the finer than in coarser grained sediments. A ubiquitous, but minor input of petroleum-related contamination with a uniform composition was evident in all samples as revealed by the analysis of petroleum biomarkers. This study demonstrates that the investigation of different classes of riverine OM

  1. Urban atmospheres.

    Science.gov (United States)

    Gandy, Matthew

    2017-07-01

    What is an urban atmosphere? How can we differentiate an 'atmosphere' from other facets of urban consciousness and experience? This essay explores some of the wider cultural, political, and philosophical connotations of atmospheres as a focal point for critical reflections on space and subjectivity. The idea of an 'affective atmosphere' as a distinctive kind of mood or shared corporeal phenomenon is considered in relation to recent developments in phenomenology, extended conceptions of agency, and new understandings of materialism. The essay draws in particular on the changing characteristics of air and light to reflect on different forms of sensory experience and their wider cultural and political connotations. The argument highlights some of the tensions and anomalies that permeate contemporary understandings of urban atmospheres.

  2. Particulate Matter Assessment in the Air Based on the Heavy Metals Presence

    Directory of Open Access Journals (Sweden)

    Jandačka Dušan

    2014-05-01

    Full Text Available Particulate matters are the result of various processes in the atmosphere that are part of everyday life. The chemical composition of these particles is mainly influenced by their origin. Their behavior is also dependent on meteorological conditions and other factors as well. The aim of this paper was to identify sources of particulate matters by means of statistical methods due to the presence of 17 heavy metals. The problem solving assumes the knowledge of multivariate statistical data analysis methods as principal components analysis (PCA, factor analysis (FA and multivariate regression and vector algebra. For the application of methodology suitable software may prove appropriate.

  3. Notes on the Particulate Matter Standards in the European Union and the Netherlands

    Directory of Open Access Journals (Sweden)

    Hugo Priemus

    2009-03-01

    Full Text Available The distribution of Particulate Matter in the atmosphere, resulting from emissions produced by cars, trucks, ships, industrial estates and agricultural complexes, is a topical public health problem that has increased in recent decades due to environmental factors in advanced economies in particular. This contribution relates the health impact caused by concentrations of Particulate Matter (PM in ambient air to the PM standards, the size of the particles and spatial planning. Diverging impacts of PM standards in legal regulation are discussed. The authors present a review of the development of legal PM standards in the European Union, with a specific reference to The Netherlands.

  4. Occurrence, gas/particle partitioning and carcinogenic risk of polycyclic aromatic hydrocarbons and their oxygen and nitrogen containing derivatives in Xi'an, central China

    Energy Technology Data Exchange (ETDEWEB)

    Wei, Chong [Key Laboratory of Aerosol Chemistry and Physics (KLACP), Institute of Earth Environment, Chinese Academy of Sciences, Xi' an 710075 (China); Geographic Institute, University of Berne, Hallerstrasse 12, 3012 Berne (Switzerland); State Key Laboratory of Loess and Quaternary Geology (SKLLQG), Institute of Earth Environment, Chinese Academy of Sciences, Xi' an 710075 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Han, Yongming, E-mail: yongming@ieecas.cn [Key Laboratory of Aerosol Chemistry and Physics (KLACP), Institute of Earth Environment, Chinese Academy of Sciences, Xi' an 710075 (China); State Key Laboratory of Loess and Quaternary Geology (SKLLQG), Institute of Earth Environment, Chinese Academy of Sciences, Xi' an 710075 (China); Bandowe, Benjamin A. Musa [Geographic Institute, University of Berne, Hallerstrasse 12, 3012 Berne (Switzerland); Cao, Junji [Key Laboratory of Aerosol Chemistry and Physics (KLACP), Institute of Earth Environment, Chinese Academy of Sciences, Xi' an 710075 (China); State Key Laboratory of Loess and Quaternary Geology (SKLLQG), Institute of Earth Environment, Chinese Academy of Sciences, Xi' an 710075 (China); Institute of Global Environmental Change, Xi' an Jiaotong University, Xi' an 710049 (China); Huang, Ru-Jin [Key Laboratory of Aerosol Chemistry and Physics (KLACP), Institute of Earth Environment, Chinese Academy of Sciences, Xi' an 710075 (China); Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, 5232 Villigen PSI (Switzerland); Ni, Haiyan; Tian, Jie [Key Laboratory of Aerosol Chemistry and Physics (KLACP), Institute of Earth Environment, Chinese Academy of Sciences, Xi' an 710075 (China); State Key Laboratory of Loess and Quaternary Geology (SKLLQG), Institute of Earth Environment, Chinese Academy of Sciences, Xi' an 710075 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); and others

    2015-02-01

    29 parent- and alkyl-polycyclic aromatic hydrocarbons (PAHs), 15 oxygenated-PAHs (OPAHs), 11 nitrated-PAHs (NPAHs) and 4 azaarenes (AZAs) in both the gaseous and particulate phases, as well as the particulate-bound carbon fractions (organic carbon, elemental carbon, char, and soot) in ambient air sampled in March and September 2012 from an urban site in Xi'an, central China were extracted and analyzed. The average concentrations (gaseous + particulate) of ∑ 29PAHs, ∑ 15OPAHs, ∑ 11NPAHs and ∑ 4AZAs were 1267.0 ± 307.5, 113.8 ± 46.1, 11.8 ± 4.8 and 26.5 ± 11.8 ng m{sup −3} in March and 784.7 ± 165.1, 67.2 ± 9.8, 9.0 ± 1.5 and 21.6 ± 5.1 ng m{sup −3} in September, respectively. Concentrations of ∑ 29PAHs, ∑ 15OPAHs and ∑ 11NPAHs in particulates were significantly correlated with those of the carbon fractions (OC, EC, char and soot). Both absorption into organic matter in particles and adsorption onto the surface of particles were important for PAHs and OPAHs in both sampling periods, with more absorption occurring in September, while absorption was always the most important process for NPAHs. The total carcinogenic risk of PAHs plus the NPAHs was higher in March. Gaseous compounds, which were not considered in most previous studies, contributed 29 to 44% of the total health risk in March and September, respectively. - Highlights: • Gaseous and particulate PAHs, OPAHs, NPAHs and AZAs were measured at Xi’an. • ∑29PAHs were 1 to 2 orders of magnitude higher than ∑15OPAHs, ∑11NPAHs and ∑4AZAs. • MW can predict phase partitioning and more absorption occurred in September. • Gaseous PACs contributed 29 − 44% of total cancer risk.

  5. Dans le tourbillon des particules

    CERN Document Server

    Zito, Marco

    2015-01-01

    Accélérateurs géants, détecteurs complexes, particules énigmatiques... La physique subatomique peut sembler bien intimidante pour le novice. Et pourtant, qui n a jamais entendu parler du boson de Higgs et du CERN, le laboratoire européen où il a été découvert en 2012 ? Nul besoin d être un spécialiste pour comprendre de quoi il s agit. Aujourd hui, une théorie extraordinairement élégante, le Modèle Standard, décrit tous les résultats des expériences dans le domaine. Trente-sept particules élémentaires et quatre forces fondamentales : c est tout ce dont nous avons besoin pour expliquer la matière et l Univers ! Ce livre, destiné à un large public, raconte sans équations le long parcours qui a abouti au Modèle Standard. Ce parcours, parfois sinueux, a été entamé lorsque les Grecs anciens, et peut-être d autres avant eux, ont imaginé que la matière est composée de petites « billes ». Il faudra attendre plusieurs siècles pour qu on réalise que la matière, à l échelle micros...

  6. Southern Fine Particulate Monitoring Project

    Energy Technology Data Exchange (ETDEWEB)

    Ashley Williamson

    2003-05-31

    This final project report presents experimental details, results and analysis of continuous onsite ambient fine particulate data at the North Birmingham sampling site during the October, 2001-September, 2002 study period.The host site for these measurement activities is the North Birmingham PM monitoring station by the Jefferson County Health Department in Birmingham, AL.The continuous data include PM{sub 2.5} mass concentrations measured by TEOM, particle sulfate using the R&P 8400S monitor, particle size distributions measured by SMPS and APS monitors, and PM{sub 2.5} light scattering extinction coefficient as measured by nephelometer. During the course of the project, measurement intercomparison data were developed for these instruments and several complementary measurements at the site. The report details the instrument set and operating procedures and describes the resulting data. Report subsections present an overview summary of the data, followed by detailed description of the systematic time behavior of PM{sub 2.5} and other specific particulate size fractions. Specific subsections are included for particle size distribution, light scattering, and particle sulfate data. The final subsection addresses application of the measurements to the practical questions of fine PM generation and transport, source attribution, and PM{sub 2.5} management strategies.

  7. PARTICULATE MATTER, OXIDATIVE STRESS AND ...

    Science.gov (United States)

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

  8. 23 Elemental Composition of Suspended Particulate Matter ...

    African Journals Online (AJOL)

    `123456789jkl''''#

    Elemental Composition of Suspended Particulate Matter Collected at Two Different. Heights above the Ground in A Sub-Urban Site in Kenya. Gitari W. M1, Kinyua A. M. 2, Kamau G. N3 and C. K. Gatebe C. K4. Abstract. Suspended particulate matter samples were collected in a sub-urban area in Nairobi over a 12 month ...

  9. Particulate carbohydrates in the Bay of Bengal

    Digital Repository Service at National Institute of Oceanography (India)

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

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

  10. Atmospheric Infancy

    DEFF Research Database (Denmark)

    Roald, Tone; Pedersen, Ida Egmose; Levin, Kasper

    2017-01-01

    In this article we establish intersubjective meaning-making in infancy as atmospheric. Through qualitative descriptions of five mother–infant dyads in a video-recorded, experimental setting when the infant is 4, 7, 10, and 13 months, we discovered atmospheric appearances with a developmental...... pattern of atmospheric variations. These appearances, we argue, are contextual and intersubjective monologues. The monologues are similar to what Daniel Stern describes with his concept of “vitality affects,” but they arise as a unified force that envelops the mother and child. As such, we present a new...

  11. Biomarkers of Exposure to Polycyclic Aromatic Hydrocarbons and Cognitive Function among Elderly in the United States (National Health and Nutrition Examination Survey: 2001-2002.

    Directory of Open Access Journals (Sweden)

    Elizabeth A Best

    Full Text Available Recent studies report a link between common environmental exposures, such as particulate matter air pollution and tobacco smoke, and decline in cognitive function. The purpose of this study was to assess the association between exposure to polycyclic aromatic hydrocarbons (PAHs, a selected group of chemicals present in particulate matter and tobacco smoke, and measures of cognitive performance among elderly in the general population. This cross-sectional analysis involved data from 454 individuals aged 60 years and older from the 2001-2002 National Health and Nutrition Examination Survey. The association between PAH exposures (as measured by urinary biomarkers and cognitive function (digit symbol substitution test (DSST was assessed using multiple linear regression analyses. After adjusting for age, socio-economic status and diabetes we observed a negative association between urinary 1-hydroxypyrene, the gold standard of PAH exposure biomarkers, and DSST score. A one percent increase in urinary 1-hydroxypyrene resulted in approximately a 1.8 percent poorer performance on the digit symbol substitution test. Our findings are consistent with previous publications and further suggest that PAHs, at least in part may be responsible for the adverse cognitive effects linked to tobacco smoke and particulate matter air pollution.

  12. Advanced Fine Particulate Characterization Methods

    Energy Technology Data Exchange (ETDEWEB)

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

    2007-01-31

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

  13. Atmospheric science and power production

    Energy Technology Data Exchange (ETDEWEB)

    Randerson, D. (ed.)

    1984-07-01

    This is the third in a series of scientific publications sponsored by the US Atomic Energy Commission and the two later organizations, the US Energy Research and Development Adminstration, and the US Department of Energy. The first book, Meteorology and Atomic Energy, was published in 1955; the second, in 1968. The present volume is designed to update and to expand upon many of the important concepts presented previously. However, the present edition draws heavily on recent contributions made by atmospheric science to the analysis of air quality and on results originating from research conducted and completed in the 1970s. Special emphasis is placed on how atmospheric science can contribute to solving problems relating to the fate of combustion products released into the atmosphere. The framework of this book is built around the concept of air-quality modeling. Fundamentals are addressed first to equip the reader with basic background information and to focus on available meteorological instrumentation and to emphasize the importance of data management procedures. Atmospheric physics and field experiments are described in detail to provide an overview of atmospheric boundary layer processes, of how air flows around obstacles, and of the mechanism of plume rise. Atmospheric chemistry and removal processes are also detailed to provide fundamental knowledge on how gases and particulate matter can be transformed while in the atmosphere and how they can be removed from the atmosphere. The book closes with a review of how air-quality models are being applied to solve a wide variety of problems. Separate analytics have been prepared for each chapter.

  14. Methods for Coating Particulate Material

    Science.gov (United States)

    Littman, Howard (Inventor); Plawsky, Joel L. (Inventor); Paccione, John D. (Inventor)

    2013-01-01

    Methods and apparatus for coating particulate material are provided. The apparatus includes a vessel having a top and a bottom, a vertically extending conduit having an inlet in the vessel and an outlet outside of the vessel, a first fluid inlet in the bottom of the vessel for introducing a transfer fluid, a second fluid inlet in the bottom of the vessel for introducing a coating fluid, and a fluid outlet from the vessel. The method includes steps of agitating a material, contacting the material with a coating material, and drying the coating material to produce a coated material. The invention may be adapted to coat aerogel beads, among other materials. A coated aerogel bead and an aerogel-based insulation material are also disclosed.

  15. Cytotoxicity and genotoxicity of urban particulate matter in mammalian cells.

    Science.gov (United States)

    Dumax-Vorzet, Audrey F; Tate, M; Walmsley, Richard; Elder, Rhod H; Povey, Andrew C

    2015-09-01

    Ambient air particulate matter (PM)-associated reactive oxygen species (ROS) have been linked to a variety of altered cellular outcomes. In this study, three different PM samples from diesel exhaust particles (DEPs), urban dust standard reference material SRM1649a and air collected in Manchester have been tested for their ability to oxidise DNA in a cell-free assay, to increase intracellular ROS levels and to induce CYP1A1 gene expression in mammalian cells. In addition, the cytotoxicity and genotoxicity of PM were assessed using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and alkaline comet assay, respectively. All PM samples catalysed the Fenton reaction in a cell-free assay, but only DEP resulted in the generation of ROS as measured by dichlorodihydrofluorescein diacetate oxidation in mammalian cells. However, there was no evidence that increased ROS was a consequence of polycyclic aromatic hydrocarbon metabolism via CYP1A1 induction as urban dust, the Manchester dust samples but not DEP-induced CYP1A1 expression. Urban dust was more cytotoxic in murine embryonic fibroblasts (MEFs) than the other PM samples and also induced expression of GADD45a in the GreenScreen Human Cell assay without S9 activation suggesting the presence of a direct-acting genotoxicant. Urban dust and DEP produced comparable levels of DNA damage, as assessed by the alkaline comet assay, in MEFs at higher levels than those induced by Manchester PM. In conclusion, results from the cytotoxic and genotoxic assays are not consistent with ROS production being the sole determinant of PM-induced toxicity. This suggests that the organic component can contribute significantly to this toxicity and that further work is required to better characterise the extent to which ROS and organic components contribute to PM-induced toxicity. © The Author 2015. Published by Oxford University Press on behalf of the UK Environmental Mutagen Society.

  16. Study of the combustion of aluminium and magnesium particulates: influence of the composition of the gaseous mixture and of pressure; Etude de la combustion de particules d'aluminium et de magnesium: influence de la composition du melange gazeux et de la pression

    Energy Technology Data Exchange (ETDEWEB)

    Legrand, B.

    2000-07-01

    The combustion of metal particulates has a major interest in the domain of space propulsion. Aluminium is today used as doping material in the solid propellant of Ariane 5 rocket engines. Magnesium represents a possible fuel for propellers allowing a come back from Mars. An electrostatic levitation device has been used to study the combustion in controlled environment of particulates having a size representative of those encountered in propellers. The particulates are ignited with a laser and observed by fast cinematography. The inhibitive property of hydrogen chloride, an important constituent of the propellant atmosphere, on the combustion of aluminium particulates has been evidenced. These results have been compared with those obtained with a kinetic model in gaseous phase. The combustion of magnesium particulates in carbon dioxide has been studied for 53-63 {mu}m and 1-2 mm particulates. It is shown that the ignition of small particulates is controlled by the chemical kinetics and that the limit ignition pressure is reversely proportional to the particulates size. A study on big samples, performed in normal gravity but also in reduced gravity to get rid of the natural convection phenomena, has permitted to show a pulsed combustion regime linked with the presence of heterogenous reactions. The measurement of the combustion durations for the different sizes of particulates has permitted to propose a correlation between these two parameters for the particulate diameters comprised between 50 {mu}m and 2 mm. (J.S.)

  17. Assessing the polycyclic aromatic hydrocarbon (PAH) pollution of urban stormwater runoff: a dynamic modeling approach.

    Science.gov (United States)

    Zheng, Yi; Lin, Zhongrong; Li, Hao; Ge, Yan; Zhang, Wei; Ye, Youbin; Wang, Xuejun

    2014-05-15

    Urban stormwater runoff delivers a significant amount of polycyclic aromatic hydrocarbons (PAHs), mostly of atmospheric origin, to receiving water bodies. The PAH pollution of urban stormwater runoff poses serious risk to aquatic life and human health, but has been overlooked by environmental modeling and management. This study proposed a dynamic modeling approach for assessing the PAH pollution and its associated environmental risk. A variable time-step model was developed to simulate the continuous cycles of pollutant buildup and washoff. To reflect the complex interaction among different environmental media (i.e. atmosphere, dust and stormwater), the dependence of the pollution level on antecedent weather conditions was investigated and embodied in the model. Long-term simulations of the model can be efficiently performed, and probabilistic features of the pollution level and its risk can be easily determined. The applicability of this approach and its value to environmental management was demonstrated by a case study in Beijing, China. The results showed that Beijing's PAH pollution of road runoff is relatively severe, and its associated risk exhibits notable seasonal variation. The current sweeping practice is effective in mitigating the pollution, but the effectiveness is both weather-dependent and compound-dependent. The proposed modeling approach can help identify critical timing and major pollutants for monitoring, assessing and controlling efforts to be focused on. The approach is extendable to other urban areas, as well as to other contaminants with similar fate and transport as PAHs. Copyright © 2014 Elsevier B.V. All rights reserved.

  18. Local-Scale Atmospheric Reactive Flow Simulations

    Energy Technology Data Exchange (ETDEWEB)

    Westbrook, C K; Lee, R L

    2005-03-29

    A computer model was developed to simulate the spatial and chemical evolution of gaseous and aerosol chemicals released into the atmosphere. The evolution is followed over the range of a few kilometers, in environments including terrain variability, urban features including buildings, and variable winds. Submodels for both gas phase chemicals and the chemical composition of liquid and particulate aerosols are included, and preliminary tests of the model are described.

  19. Pesticide loss to the atmosphere.

    Science.gov (United States)

    Plimmer, J R

    1990-01-01

    Pesticides may be transformed by chemical and biological processes or transported from the site of application by several processes including runoff, movement through the soil to ground water, volatilization, transport on soil particles, and wind erosion. Contamination of water by pesticide residues is a matter of concern as is contamination of the earth's atmosphere. The form in which a pesticide enters the air and the dimensions of pesticide-containing particulate matter affect movement and deposition. Local transport over distances of several miles may be responsible for adverse effects on nontarget species. Effects of long-range transport are more difficult to assess, but pesticides increase the burden of organic chemicals in the atmosphere. Field measurements of pesticide volatilization and deposition of residues in rainfall, particulate matter, fog, etc., provide information on the relative importance of these processes. Adequate information concerning chemical reactions of pesticides in air is lacking. Because it is desirable to minimize low-level human and environmental exposure resulting from airborne pesticide residues, potential for losses to the air should be taken into account in selecting pesticide formulations and application methods.

  20. Hydrocarbons in particulate samples from wildfire events in central Portugal in summer 2010.

    Science.gov (United States)

    Vicente, Ana; Calvo, Ana; Fernandes, Ana P; Nunes, Teresa; Monteiro, Cristina; Pio, Casimiro; Alves, Célia

    2017-03-01

    In summer 2010, twenty eight (14 PM2.5 samples plus 14 samples PM2.5-10) smoke samples were collected during wildfires that occurred in central Portugal. A portable high-volume sampler was used to perform the sampling, on quartz fibre filters of coarse (PM2.5-10) and fine (PM2.5) smoke samples. The carbonaceous content (elemental and organic carbon) of particulate matter was analysed by a thermal-optical technique. Subsequently, the particulate samples were solvent extracted and fractionated by vacuum flash chromatography into three different classes of organic compounds (aliphatics, polycyclic aromatic hydrocarbons (PAHs) and carbonyl compounds). The organic speciation was performed by gas chromatography-mass spectrometry (GC-MS). Emissions were dominated by the fine particles, which represented around 92% of the PM10. A clear predominance of carbonaceous constituents was observed, with organic to elemental carbon (OC/EC) ratios ranging between 1.69 and 245 in both size fractions. The isoprenoid ketone 6,10,14-trimethyl-2-pentadecanone, a tracer for secondary organic aerosol formation, was one of the dominant constituents in both fine and coarse particles. Retene was the most abundant compound in all samples. Good correlations were obtained between OC and both aliphatic and PAH compounds. Pyrogenic processes, thermal release of biogenic compounds and secondary processing accounted for 97% of the apportioned PM2.5 levels. Copyright © 2016. Published by Elsevier B.V.

  1. Impacts of a nanosized ceria additive on diesel engine emissions of particulate and gaseous pollutants.

    Science.gov (United States)

    Zhang, Junfeng; Nazarenko, Yevgen; Zhang, Lin; Calderon, Leonardo; Lee, Ki-Bum; Garfunkel, Eric; Schwander, Stephan; Tetley, Teresa D; Chung, Kian Fan; Porter, Alexandra E; Ryan, Mary; Kipen, Howard; Lioy, Paul J; Mainelis, Gediminas

    2013-11-19

    Fuel additives incorporating nanosized ceria have been increasingly used in diesel engines as combustion promoters. However, few studies have assessed the impact of these nanotechnology-based additives on pollutant emissions. Here, we systematically compare emission rates of particulate and gaseous pollutants from a single-cylinder, four-cycle diesel engine using fuel mixes containing nanoceria of varying concentrations. The test fuels were made by adding different amounts of a commercial fuel additive Envirox into an ultralow-sulfur diesel fuel at 0 (base fuel), 0.1-, 1-, and 10-fold the manufacturer-recommended concentration of 0.5 mL Envirox per liter of fuel. The addition of Envirox resulted in ceria-concentration-dependent emission reductions of CO2, CO, total particulate mass, formaldehyde, acetaldehyde, acrolein, and several polycyclic aromatic hydrocarbons. These reductions at the manufacturer-recommended doping concentration, however, were accompanied by a substantial increase of certain other air pollutants, specifically the number of ultrafine particles (+32%), NO(x) (+9.3%), and the particle-phase benzo[a]pyrene toxic equivalence quotient (+35%). Increasing fuel ceria concentrations also led to decreases in the size of emitted particles. Given health concerns related to ultrafine particles and NO(x), our findings call for additional studies to further evaluate health risks associated with the use of nanoceria additives in various engines under various operating conditions.

  2. Contrasting biological potency of particulate matter collected at sites impacted by distinct industrial sources.

    Science.gov (United States)

    Thomson, Errol M; Breznan, Dalibor; Karthikeyan, Subramanian; MacKinnon-Roy, Christine; Vuong, Ngoc Q; Dabek-Zlotorzynska, Ewa; Celo, Valbona; Charland, Jean-Pierre; Kumarathasan, Prem; Brook, Jeffrey R; Vincent, Renaud

    2016-12-01

    Industrial sources contribute a significant proportion of anthropogenic particulate matter (PM) emissions, producing particles of varying composition that may differentially impact health. This study investigated the in vitro toxicity of ambient PM collected near industrial sites in relation to particle size and composition. Size-fractionated particles (ultrafine, PM0.1-2.5, PM2.5-10, PM>10) were collected in the vicinity of steel, copper, aluminium, and petrochemical industrial sites. Human lung epithelial-like A549 and murine macrophage-like J774A.1 cells were exposed for 24 h to particle suspensions (0, 30, 100, 300 μg/cm(2)). Particle potency was assessed using cytotoxic (resazurin reduction, lactate dehydrogenase (LDH) release) and inflammatory (cytokine release) assays, and regressed against composition (metals, polycyclic aromatic hydrocarbons (PAHs), endotoxin). Coarse (PM2.5-10, PM>10) particle fractions were composed primarily of iron and aluminium; in contrast, ultrafine and fine (PM0.1-2.5) fractions displayed considerable variability in metal composition (especially water-soluble metals) across collection sites consistent with source contributions. Semi-volatile and PM-associated PAHs were enriched in the fine and coarse fractions collected near metal industry. Cell responses to exposure at equivalent mass concentrations displayed striking differences among sites (SITE x SIZE and SITE x DOSE interactions, p Industrial sources produce particulate emissions with varying chemical composition that differ in their in vitro potency in relation to particle size and the levels of specific constituents.

  3. On-road particulate emission measurement

    Science.gov (United States)

    Mazzoleni, Claudio

    Particulate matter (PM) suspended in the atmosphere has harmful health effects, contributes to visibility impairment, and affects atmospheric radiative transfer, thereby contributing to global change. Vehicles contribute substantially to the ambient PM concentration in urban areas, yet the fraction of ambient PM originating from vehicle emissions is poorly characterized because suitable measurement methods have not been available. This dissertation describes the development and the use of a new vehicle emission remote sensing system (VERSS) for the on-road measurement of PM emission factors for vehicles. The PM VERSS measures PM by ultraviolet backscattering and transmission. PM backscattering and transmission mass efficiencies have been calculated from Mie theory based on an homogeneous spherical model for gasoline particles and on a two-layers, spherical model for diesel particles. The VERSS was used in a large-scale study in Las Vegas, NV. A commercial gaseous VERSS was used for the measurement of gaseous emission factors (i.e., carbon monoxide, hydrocarbons, and nitrogen oxide). Speed and acceleration were also measured for each vehicle. A video image of each vehicle's rear license plate was acquired and license plate numbers were matched with the Clark County department of motor vehicle database to retrieve vehicle information such as model year, vehicle weight category and engine ignition type. PM VERSS has precisely estimated PM fleet average emission factors and clearly shown the dependence of PM emission factors on vehicle model year. Under mostly hot-stabilized operation, diesel vehicle PM emission factors are about 25 times higher than those of gasoline vehicles. Furthermore, the fleet frequency distributions of PM emission factors are highly skewed, meaning that most of the fleet emission factor is accounted for by a small portion of the fleet. The PM VERSS can measure PM emission factors for these high emitting vehicles on an individual basis. PM

  4. Particulate matter and polycyclic aromatic hydrocarbons from forest fires: impacts on air quality and occupational risks assessment

    Science.gov (United States)

    Oliveira, Marta Madalena Marques de

    As piroxenas sao um vasto grupo de silicatos minerais encontrados em muitas rochas igneas e metamorficas. Na sua forma mais simples, estes silicatos sao constituidas por cadeias de SiO3 ligando grupos tetrahedricos de SiO4. A formula quimica geral das piroxenas e M2M1T2O6, onde M2 se refere a catioes geralmente em uma coordenacao octaedrica distorcida (Mg2+, Fe2+, Mn2+, Li+, Ca2+, Na+), M1 refere-se a catioes numa coordenacao octaedrica regular (Al3+, Fe3+, Ti4+, Cr3+, V3+, Ti3+, Zr4+, Sc3+, Zn2+, Mg2+, Fe2+, Mn2+), e T a catioes em coordenacao tetrahedrica (Si4+, Al3+, Fe3+). As piroxenas com estrutura monoclinica sao designadas de clinopiroxenes. A estabilidade das clinopyroxenes num espectro de composicoes quimicas amplo, em conjugacao com a possibilidade de ajustar as suas propriedades fisicas e quimicas e a durabilidade quimica, tem gerado um interesse mundial devido a suas aplicacoes em ciencia e tecnologia de materiais. Este trabalho trata do desenvolvimento de vidros e de vitro-cerâmicos baseadas de clinopiroxenas para aplicacoes funcionais. O estudo teve objectivos cientificos e tecnologicos; nomeadamente, adquirir conhecimentos fundamentais sobre a formacao de fases cristalinas e solucoes solidas em determinados sistemas vitro-cerâmicos, e avaliar a viabilidade de aplicacao dos novos materiais em diferentes areas tecnologicas, com especial enfase sobre a selagem em celulas de combustivel de oxido solido (SOFC). Com este intuito, prepararam-se varios vidros e materiais vitro-cerâmicos ao longo das juntas Enstatite (MgSiO3) - diopsidio (CaMgSi2O6) e diopsidio (CaMgSi2O6) - Ca - Tschermak (CaAlSi2O6), os quais foram caracterizados atraves de um vasto leque de tecnicas. Todos os vidros foram preparados por fusao-arrefecimento enquanto os vitro-cerâmicos foram obtidos quer por sinterizacao e cristalizacao de fritas, quer por nucleacao e cristalizacao de vidros monoliticos. Estudaram-se ainda os efeitos de varias substituicoes ionicas em composicoes de diopsidio contendo Al na estrutura, sinterizacao e no comportamento durante a cristalizacao de vidros e nas propriedades dos materiais vitro-cerâmicos, com relevância para a sua aplicacao como selantes em SOFC. Verificou-se que Foi observado que os vidros/vitro-cerâmicos a base de enstatite nao apresentavam as caracteristicas necessarias para serem usados como materiais selantes em SOFC, enquanto as melhores propriedades apresentadas pelos vitro-cerâmicos a base de diopsidio qualificaram-nos para futuros estudos neste tipo de aplicacoes. Para alem de investigar a adequacao dos vitro-cerâmicos a base de clinopyroxene como selantes, esta tese tem tambem como objetivo estudar a influencia dos agentes de nucleacao na nucleacao em volume dos vitro-cerâmicos resultantes a base de diopsidio, de modo a qualifica-los como potenciais materiais hopedeiros de residuos nucleares radioactivos.

  5. Different partition of polycyclic aromatic hydrocarbon on environmental particulates in freshwater: Microplastics in comparison to natural sediment.

    Science.gov (United States)

    Wang, Wenfeng; Wang, Jun

    2018-01-01

    Microplastics pollution in the aquatic ecosystems has aroused increasing concerns in recent years. Though microplastics are known to sorb organic contaminants from water, the interaction mechanisms between microplastics and organic chemicals are not yet well understood. Here we investigated the partition characteristics of phenanthrene (Phe) in three mass-produced plastic particles, including polyethylene (PE), polystyrene (PS) and polyvinylchloride (PVC), and one natural sediment, as a comparison. The sorption kinetics of Phe onto microplastics and natural sediment were successfully described by the pseudo-second-order model (R 2 > 0.992), while the equilibrium data were best-fitted to the Langmuir isotherm (R 2 > 0.995). Compared with natural sediment, microplastics exhibited higher capacities for Phe which followed an order of PE > PS > PVC. As the aqueous concentration of pyrene (Pyr) increased, both uptakes and distribution coefficients (K d ) of Phe within the solids decreased, with natural sediment giving the largest decline. Although proportions of Phe desorbed from the contaminated microplastics were low, due to the high Phe uptake, microplastics released larger amounts of the sorbed Phe to water than the natural sediment during the desorption process. Given their minimal abundance relative to natural sediment, microplastics may play a less important role in the transport of organic pollutants in a natural aquatic environment. Copyright © 2017 Elsevier Inc. All rights reserved.

  6. Atmospheric neutrinos

    Energy Technology Data Exchange (ETDEWEB)

    Kajita, Takaaki [Research Center for Cosmic Neutrinos, Institute for Cosmic Ray Research, University of Tokyo, Kashiwa-no-ha 5-1-5, Kashiwa, Chiba 277-8582 (Japan)

    2004-12-01

    Neutrino oscillation was discovered through the study of atmospheric neutrinos. Atmospheric neutrinos are produced as decay products in hadronic showers resulting from collisions of cosmic rays with nuclei in the atmosphere. Electron neutrinos and muon neutrinos are produced mainly by the decay chain of charged pions to muons and electrons. Depending on the energy of the neutrinos, atmospheric neutrinos are observed as fully contained events, partially contained events and upward-going muon events. The energy range covered by these events is from a few hundred MeV to >1 TeV. Data from various experiments showed zenith angle- and energy-dependent deficit of {nu}{sub {mu}} events, while {nu}{sub e} events did not show any such effect. It was also shown that the {nu}{sub {mu}} survival probability obeys the sinusoidal function as predicted by neutrino oscillations. Two-flavour {nu}{sub {mu}} {r_reversible} {nu}{sub {tau}} oscillations, with sin{sup 2} 2{theta} > 0.90 and {delta}m{sup 2} in the region of 1.9 x 10{sup -3} to 3.0 x 10{sup -3} eV{sup 2}, explain all these data. Various detailed studies using high statistics atmospheric neutrino data excluded the alternative hypotheses that were proposed to explain the {nu}{sub {mu}} deficit.

  7. Quantum transport through polycyclic hydrocarbon molecules: Green's function approach

    OpenAIRE

    Maiti, Santanu K.

    2009-01-01

    Quantum transport properties through single polycyclic hydrocarbon molecules attached to two metallic electrodes are studied by the use of Green's function technique. A parametric approach based on the tight-binding model is introduced to investigate the electronic transport through such molecular bridge systems. The transport properties are discussed in the aspects of (a) molecule-to-electrode coupling strength and (b) quantum interference effect.

  8. THE INFRARED SPECTROSCOPY OF NEUTRAL POLYCYCLIC AROMATIC HYDROCARBON CLUSTERS

    Energy Technology Data Exchange (ETDEWEB)

    Ricca, Alessandra [Carl Sagan Center, SETI Institute, 189 Bernardo Avenue, Suite 100, Mountain View, CA 94043 (United States); Bauschlicher, Charles W. Jr. [Entry Systems and Technology Division, Mail Stop 230-3, NASA Ames Research Center, Moffett Field, CA 94035 (United States); Allamandola, Louis J., E-mail: Alessandra.Ricca-1@nasa.gov, E-mail: Charles.W.Bauschlicher@nasa.gov [Space Science Division, Mail Stop 245-6, NASA Ames Research Center, Moffett Field, CA 94035 (United States)

    2013-10-10

    The mid-infrared spectra of neutral homogeneous polycyclic aromatic hydrocarbon (PAH) clusters have been computed using density functional theory including an empirical correction for dispersion. The C-H out-of-plane bending modes are redshifted for all the clusters considered in this work. The magnitude of the redshift and the peak broadening are dependent on PAH size, shape, and on the PAH arrangement in the cluster.

  9. Polycyclic aromatic hydrocarbons in cryogenic peat plateaus of northeastern Europe

    Science.gov (United States)

    Pastukhov, A. V.; Kaverin, D. A.; Gabov, D. N.

    2017-07-01

    The qualitative and quantitative composition of 14 polycyclic aromatic hydrocarbons (PAHs) in peat plateaus at the southern boundary of the permafrost zone in northeastern Europe, where degradation of permafrost occurs because of climate warming, has been studied by high-performance liquid chromatography in gradient mode. PAH concentrations vary from 150 to 3700 ng/g with their average content of about 1500 ± 1000 ng/g. The variation of data is primarily due to the large contribution of heavy PAHs.

  10. Electrically heated particulate filter enhanced ignition strategy

    Science.gov (United States)

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

    2012-10-23

    An exhaust system that processes exhaust generated by an engine is provided. The system generally includes a particulate filter (PF) that filters particulates from the exhaust wherein an upstream end of the PF receives exhaust from the engine. A grid of electrically resistive material is applied to an exterior upstream surface of the PF and selectively heats exhaust passing through the grid to initiate combustion of particulates within the PF. A catalyst coating applied to at least one of the PF and the grid. A control module estimates a temperature of the grid and controls the engine to produce a desired exhaust product to increase the temperature of the grid.

  11. Energy sources of polycyclic aromatic hydrocarbons. [Carcinogenicity of PAHs

    Energy Technology Data Exchange (ETDEWEB)

    Guerin, M. R.

    1977-01-01

    Combustion is the predominant end-process by which fossil fuels are converted to energy. Combustion, particularly when inefficient, is also the primary technological source of polycyclic aromatic hydrocarbons (PAHs) released into the environment. The need for liquid fuels to supply the transportation industry and for nonpolluting fuels for heat and power generation provide the incentive to commercialize processes to convert coal to substitute natural gas and oil. These processes represent a potentially massive new source of environmental PAHs. Insuring an adequate supply of energy with minimum impact on the environment and on health is one of the most important, urgent, and challenging goals currently facing science and technology. Polycyclic aromatic hydrocarbon related carcinogenesis is among the most important of possible occupational- and environmental-health impacts of much of the current and projected national energy base. An understanding of the relationship of polycyclic aromatic hydrocarbons (PAHs) to human cancer and a continued surveillance of energy sources for PAH content are necessary to minimize this impact.

  12. Microbial degradation of petrochemical waste-polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Fulekar, M H

    2017-01-01

    Petrochemical industry is one of the fastest growing industries. This industry has immense importance in the growth of economy and manufacture of large varieties of chemicals. The petrochemical industry is a hazardous group of industry generating hazardous waste containing organic and inorganic compounds. In spite of the present treatment process, the hazardous waste compounds are found untreated to the acceptable level and found discharged at soil-water environment resulting into the persistent organic-inorganic pollutant into the environment. The bioremediation will be the innovative techniques to remove the persistent pollutants in the environment. Petrochemical contaminated site was found to be a rich source of microbial consortium degrading polycyclic aromatic hydrocarbons. Indigenous microbial consortiums were identified and used for bioremediation of polycyclic aromatic hydrocarbons (naphthalene and anthracene) at the concentrations of 250, 500, and 750 ppm. The potential microorganism was also identified for naphthalene and anthracene, and their bioremediation was studied at varying concentrations. The bioremediation with consortium was found to be comparatively more effective than the potential microorganism used for bioremediation of each compound. Pseudomonas aeruginosa a potential organism was identified by 16S rRNA and further studied for the gene responsible for the PAH compounds. Indigenous microorganism as a consortium has been found effective and efficient source for remediation of organic compound-Polycyclic aromatic hydrocarbon and this will also be applicable to remediate the toxic compounds to clean up the environment.

  13. Atmospheric thermodynamics

    CERN Document Server

    Iribarne, J V

    1973-01-01

    The thermodynamics of the atmosphere is the subject of several chapters in most textbooks on dynamic meteorology, but there is no work in English to give the subject a specific and more extensive treatment. In writing the present textbook, we have tried to fill this rather remarkable gap in the literature related to atmospheric sciences. Our aim has been to provide students of meteorology with a book that can playa role similar to the textbooks on chemical thermodynamics for the chemists. This implies a previous knowledge of general thermodynamics, such as students acquire in general physics courses; therefore, although the basic principles are reviewed (in the first four chapters), they are only briefly discussed, and emphasis is laid on those topics that will be useful in later chapters, through their application to atmospheric problems. No attempt has been made to introduce the thermodynamics of irreversible processes; on the other hand, consideration of heterogeneous and open homogeneous systems permits a...

  14. Sources of organic pollution in particulate matter and soil of Silesian Agglomeration (Poland): evidence from geochemical markers.

    Science.gov (United States)

    Fabiańska, Monika J; Kozielska, Barbara; Konieczyński, Jan; Kowalski, Adam

    2016-06-01

    The exact input of particular sources to polycyclic aromatic hydrocarbons (PAHs) concentrations in urban and industrial agglomerations is still not well recognized. The major breakthrough is possible using geochemical markers. In the air aerosol and soil samples from areas located in the direct influence of industry/traffic in Silesian Agglomeration (Poland), PAHs and other organic compounds were analyzed, including geochemical markers (biomarkers) and polar compounds from fossil fuels and biomass. Gas chromatography (GC-FID) and gas chromatography-mass spectrometry (GC-MS) were applied to investigate the composition of particulate matter and soil extracts. The results suggest that the predominant source of PAHs is fossil fuel. The presence and distribution of steranes, pentacyclic triterpenoids (i.e., hopanes and moretanes) and alkyl PAHs point to traffic emissions and fossil fuel combustion, mainly bituminous coal for power and heat purposes, as the main source of PAHs in the region. Moreover, the presence of fossil fuel biomarker in particulate matter and soil extracts from a rural site, previously considered to be free of organic pollution, requires a cautious interpretation for PAHs results. Apart from the fossil fuel, also other sources of contamination were identified in particulate matter extracts by their markers: phenols and levoglucosan for biomass and diisopropylnaphthalenes for printing materials combustion. The absence of polar biomass combustion indicators in soil extracts might be related to their higher reactivity.

  15. Determination of Polycyclic Aromatic Hydrocarbons in Water Using Nanoporous Material Prepared from Waste Avian Egg Shell

    National Research Council Canada - National Science Library

    Nuhu, Abdulmumin A; Basheer, Chanbasha; Shaikh, Amjad Ashfaque; Al-Arfaj, Abdul Rahman

    2012-01-01

      For the first time a biocompatible calcium carbonate vateritic polymorph was recrystallized from eggshell waste and its application for the extraction of polycyclic aromatic hydrocarbons in water...

  16. Physico-Chemical Speciation and Ocean Fluxes of Polycyclic Aromatic Hydrocarbons

    National Research Council Canada - National Science Library

    Gustafsson, Orjan

    1997-01-01

    Partitioning of ecotoxicologically significant polycyclic aromatic hydrocarbons (PAHs) to non-aqueous, particularly colloidal and soot, phases results in a decrease in their, directly bioavailable, dissolved fractions...

  17. Polycyclic aromatic hydrocarbons, brachial artery distensibility and blood pressure among children residing near an oil refinery.

    Science.gov (United States)

    Trasande, Leonardo; Urbina, Elaine M; Khoder, Mamdouh; Alghamdi, Mansour; Shabaj, Ibrahim; Alam, Mohammed S; Harrison, Roy M; Shamy, Magdy

    2015-01-01

    Polycyclic aromatic hydrocarbons (PAH) are produced by the burning and processing of fuel oils, and have been associated with oxidant stress, insulin resistance and hypertension in adults. Few studies have examined whether adolescents are susceptible to cardiovascular effects of PAHs. To study associations of PAH exposure with blood pressure (BP) and brachial artery distensibility (BAD), an early marker of arterial wall stiffness, in young boys attending three schools in Jeddah, Saudi Arabia in varying proximity to an oil refinery. Air samples collected from the three schools were analyzed for PAHs. PAH metabolites (total hydroxyphenanthrenes and 1-hydroxypyrene) were measured in urine samples from 184 adolescent males, in whom anthropometrics, heart rate, pulse pressure, brachial artery distensibility and blood pressure were measured. Descriptive, bivariate and multivariable analyses were performed to assess relationships of school location and urinary PAH metabolites with cardiovascular measures. Total suspended matter was significantly higher (444 ± 143 μg/m(3)) at the school near the refinery compared to a school located near a ring road (395 ± 65 μg/m(3)) and a school located away from vehicle traffic (232 ± 137 μg/m(3)), as were PAHs. Systolic (0.47 S D units, p = 0.006) and diastolic (0.53 SD units, p refinery, with a 4.36-fold increase in prehypertension (p = 0.001), controlling for confounders. No differences in pulse pressure, BAD and heart rate were noted in relationship to school location. Urinary total hydroxyphenanthrenes and 1-hydroxypyrene were not associated with cardiovascular outcomes. Proximity to an oil refinery in Saudi Arabia is associated with prehypertension and increases in PAH and particulate matter exposures. Further study including insulin resistance measurements, better control for confounding, and longitudinal measurement is indicated. Copyright © 2014 Elsevier Inc. All rights reserved.

  18. Physicochemical characterization of particulate emissions from a compression ignition engine: the influence of biodiesel feedstock.

    Science.gov (United States)

    Surawski, N C; Miljevic, B; Ayoko, G A; Elbagir, S; Stevanovic, S; Fairfull-Smith, K E; Bottle, S E; Ristovski, Z D

    2011-12-15

    This study undertook a physicochemical characterization of particle emissions from a single compression ignition engine operated at one test mode with 3 biodiesel fuels made from 3 different feedstocks (i.e., soy, tallow, and canola) at 4 different blend percentages (20%, 40%, 60%, and 80%) to gain insights into their particle-related health effects. Particle physical properties were inferred by measuring particle number size distributions both with and without heating within a thermodenuder (TD) and also by measuring particulate matter (PM) emission factors with an aerodynamic diameter less than 10 μm (PM(10)). The chemical properties of particulates were investigated by measuring particle and vapor phase Polycyclic Aromatic Hydrocarbons (PAHs) and also Reactive Oxygen Species (ROS) concentrations. The particle number size distributions showed strong dependency on feedstock and blend percentage with some fuel types showing increased particle number emissions, while others showed particle number reductions. In addition, the median particle diameter decreased as the blend percentage was increased. Particle and vapor phase PAHs were generally reduced with biodiesel, with the results being relatively independent of the blend percentage. The ROS concentrations increased monotonically with biodiesel blend percentage but did not exhibit strong feedstock variability. Furthermore, the ROS concentrations correlated quite well with the organic volume percentage of particles - a quantity which increased with increasing blend percentage. At higher blend percentages, the particle surface area was significantly reduced, but the particles were internally mixed with a greater organic volume percentage (containing ROS) which has implications for using surface area as a regulatory metric for diesel particulate matter (DPM) emissions.

  19. 40 CFR 60.422 - Standards for particulate matter.

    Science.gov (United States)

    2010-07-01

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

  20. Heat and mass transfer in particulate suspensions

    CERN Document Server

    Michaelides, Efstathios E (Stathis)

    2013-01-01

    Heat and Mass Transfer in Particulate Suspensions is a critical review of the subject of heat and mass transfer related to particulate Suspensions, which include both fluid-particles and fluid-droplet Suspensions. Fundamentals, recent advances and industrial applications are examined. The subject of particulate heat and mass transfer is currently driven by two significant applications: energy transformations –primarily combustion – and heat transfer equipment. The first includes particle and droplet combustion processes in engineering Suspensions as diverse as the Fluidized Bed Reactors (FBR’s) and Internal Combustion Engines (ICE’s). On the heat transfer side, cooling with nanofluids, which include nanoparticles, has attracted a great deal of attention in the last decade both from the fundamental and the applied side and has produced several scientific publications. A monograph that combines the fundamentals of heat transfer with particulates as well as the modern applications of the subject would be...

  1. Diesel Particulate Matter Polygons, Arizona, 2005, NATA

    Data.gov (United States)

    U.S. Environmental Protection Agency — The national-scale assessment includes 177 air pollutants (a subset of the air toxics on the Clean Air Act's list of 187 air toxics plus diesel particulate matter...

  2. PARTICULATE MATTER, OXIDATIVE STRESS AND NEUROTOXICITY

    Science.gov (United States)

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

  3. Self-Cleaning Particulate Air Filter Project

    Data.gov (United States)

    National Aeronautics and Space Administration — NASA requires an innovative solution to the serious issue of particulate fouling on air revitalization component surfaces in order to address the potential for...

  4. Johns Hopkins Particulate Matter Research Center

    Data.gov (United States)

    Federal Laboratory Consortium — The Johns Hopkins Particulate Matter Research Center will map health risks of PM across the US based on analyses of national databases on air pollution, mortality,...

  5. Diesel Particulate Matter Polygons, Hawaii, 2005, NATA

    Data.gov (United States)

    U.S. Environmental Protection Agency — The national-scale assessment includes 177 air pollutants (a subset of the air toxics on the Clean Air Act's list of 187 air toxics plus diesel particulate matter...

  6. Diesel Particulate Matter Polygons, Nevada, 2005, NATA

    Data.gov (United States)

    U.S. Environmental Protection Agency — The national-scale assessment includes 177 air pollutants (a subset of the air toxics on the Clean Air Act's list of 187 air toxics plus diesel particulate matter...

  7. Diesel Particulate Matter Polygons, California, 2005, NATA

    Data.gov (United States)

    U.S. Environmental Protection Agency — The national-scale assessment includes 177 air pollutants (a subset of the air toxics on the Clean Air Act's list of 187 air toxics plus diesel particulate matter...

  8. Allegheny County Particulate Matter 2.5

    Data.gov (United States)

    Allegheny County / City of Pittsburgh / Western PA Regional Data Center — The U.S. Environmental Protection Agency provides information on the particulate matter concentration for Allegheny County that have a diameter greater or equal to...

  9. Respirable particulate monitoring with remote sensors. (Public health ecology: Air pollution)

    Science.gov (United States)

    Severs, R. K.

    1974-01-01

    The feasibility of monitoring atmospheric aerosols in the respirable range from air or space platforms was studied. Secondary reflectance targets were located in the industrial area and near Galveston Bay. Multichannel remote sensor data were utilized to calculate the aerosol extinction coefficient and thus determine the aerosol size distribution. Houston Texas air sampling network high volume data were utilized to generate computer isopleth maps of suspended particulates and to establish the mass loading of the atmosphere. In addition, a five channel nephelometer and a multistage particulate air sampler were used to collect data. The extinction coefficient determined from remote sensor data proved more representative of wide areal phenomena than that calculated from on site measurements. It was also demonstrated that a significant reduction in the standard deviation of the extinction coefficient could be achieved by reducing the bandwidths used in remote sensor.

  10. Alarming atmospheres

    DEFF Research Database (Denmark)

    Højlund, Marie; Kinch, Sofie

    2014-01-01

    Nurses working in the Neuro-Intensive Care Unit at Aarhus University Hospital lack the tools to prepare children for the alarming atmosphere they will enter when visiting a hospitalised relative. The complex soundscape dominated by alarms and sounds from equipment is mentioned as the main stressor...

  11. Atmospheric humidity

    Science.gov (United States)

    Water vapor plays a critical role in earth's atmosphere. It helps to maintain a habitable surface temperature through absorption of outgoing longwave radiation, and it transfers trmendous amounts of energy from the tropics toward the poles by absorbing latent heat during evaporation and subsequently...

  12. Concentrations of polycyclic aromatic hydrocarbons (PAHs) and major and trace elements in simulated rainfall runoff from parking lots, Austin, Texas, 2003

    Science.gov (United States)

    Mahler, Barbara J.; Van Metre, Peter C.; Wilson, Jennifer T.

    2004-01-01

    Samples of creek bed sediment collected near seal-coated parking lots in Austin, Texas, by the City of Austin during 2001–02 had unusually elevated concentrations of polycyclic aromatic hydrocarbons (PAHs). To investigate the possibility that PAHs from seal-coated parking lots might be transported to urban creeks, the U.S. Geological Survey, in cooperation with the City of Austin, sampled runoff and scrapings from four test plots and 13 urban parking lots. The surfaces sampled comprise coal-tar-emulsion-sealed, asphalt-emulsion-sealed, unsealed asphalt, and unsealed concrete. Particulates and filtered water in runoff and surface scrapings were analyzed for PAHs. In addition, particulates in runoff were analyzed for major and trace elements. Samples of all three media from coal-tar-sealed parking lots had concentrations of PAHs higher than those from any other types of surface. The mean total PAH concentration in particulates in runoff from parking lots in use were 3,500,000, 620,000, and 54,000 micrograms per kilogram from coal-tar-sealed, asphalt-sealed, and unsealed (asphalt and concrete combined) lots, respectively. The probable effect concentration sediment quality guideline is 22,800 micrograms per kilogram. The mean total PAH (sum of detected PAHs) concentration in filtered water from parking lots in use was 8.6 micrograms per liter for coal-tar-sealed lots; the one sample analyzed from an asphalt-sealed lot had a concentration of 5.1 micrograms per liter and the one sample analyzed from an unsealed asphalt lot was 0.24 microgram per liter. The mean total PAH concentration in scrapings was 23,000,000, 820,000, and 14,000 micrograms per kilogram from coal-tar-sealed, asphalt-sealed, and unsealed asphalt lots, respectively. Concentrations of lead and zinc in particulates in runoff frequently exceeded the probable effect concentrations, but trace element concentrations showed no consistent variation with parking lot surface type.

  13. [Polycyclic aromatic hidrocarbons deposition in the Milazzo-Valle del Mela (Sicily Region, Southern Italy) high-risk area following an oil refinery fire].

    Science.gov (United States)

    Grechi, Daniele; Biggeri, Annibale

    2016-01-01

    On September 2014, a fire began within an oil refinery involving a storage tank containing several hundreds of thousands cubic meters of virgin naphtha. Mayors of neighbouring municipalities asked the Epidemiology and Prevention Society "Giulio A. Maccacaro" to carry out an environmental survey in order to evaluate what was the nature and how dangerous was suspended dust deposited by the fumes. In the following days, after fire had been extinguished we conducted a sample survey on the presence of polycyclic aromatic hydrocarbons (PAH) and metals in particulate deposited on the soil on a radius of five kilometres from the refinery and we engaged the exposed population. The Milazzo-Valle del Mela (Sicily Region, Southern Italy) high-risk area includes several industrial plants; among them, an oil refinery and a fuel powered energy plant. As reference area we selected the Sarroch municipality (Sardinia Region, Southern Italy), in the coast of the Tyrrhenian Sea, which is geographically comparable, where a large oil refinery is located and where an environmental campaign with measurement of PAH and metals in particulate matter was ongoing. Qualitatively, metal composition of particulate matter resulted similar in the Sarroch and Milazzo samples. Instead, a large excess of PAH was documented in the Milazzo samples as compared to the Sarroch ones. In conclusion, the results of the analysis of the samples of particulate matter deposited in the Milazzo area in the days immediately following the oil refinery fire showed a high quantity of PAH, carcinogenic substances which pose major hazard to population health. The greater fall-out was registered in the proximity of the burnt storage tank and the West neighbourhood, and at lesser extent in the Southern neighbourhood. As a consequence, there was a population exposure to carcinogenic substances which could have reached the food chain.

  14. Airborne Particulates over Southern Africa

    Science.gov (United States)

    2001-01-01

    This map shows the abundance of airborne particulates, or aerosols, over Southern Africa during the period August 14 - September 29, 2000. Low particle concentrations are shown in shades of blue, and high concentrations in shades of red. The results were generated from MISR imagery acquired over this time period, and processed using MISR's automated software system. The approach for deriving aerosol amount makes use of the variation of scene brightness and contrast as a function of observation angle. Black areas over the land area correspond to places where a result was not obtained, for example, due to the presence of clouds.Extensive burning of grass and shrubland for land management and agriculture comprises a principal source of these aerosols. Vegetation availability increases northward, hence the greater abundance of haze and smoke in Angola and southern Zaire. The lower aerosol abundance around Lesotho and southeastern South Africa is consistent with the higher terrain elevations near the Drakensberg Mountains.MISR was built and is managed by NASA's Jet Propulsion Laboratory, Pasadena, CA, for NASA's Office of Earth Science, Washington, DC. The Terra satellite is managed by NASA's Goddard Space Flight Center, Greenbelt, MD. JPL is a division of the California Institute of Technology.

  15. SOUTHERN FINE PARTICULATE MONITORING PROJECT

    Energy Technology Data Exchange (ETDEWEB)

    Unknown

    2002-04-01

    This quarterly report presents results and analysis of continuous onsite ambient fine particulate data at the North Birmingham sampling site during the January-March, 2002 study period. The continuous data include PM{sub 2.5} mass concentrations measured by TEOM, particle sulfate using the R&P 8400S monitor, particle size distributions measured by SMPS and APS monitors, and PM{sub 2.5} light scattering extinction coefficient as measured by nephelometer. Some instrumental issues were noted with the upgrade of the APS model 3320 are described in the report, as well as preliminary performance indications for the upgraded instrument. During the quarter preliminary data analysis and modeling studies were conducted to test the potential of the North Birmingham site data for source attribution analyses. Our initial assessment has continued to be optimistic in this regard due to the location of the site relative to several important classes of local and midrange emission sources. We anticipate that these analyses will provide good separations of the effects of major source classes and spatial source clusters, and will provide useful information relevant to PM{sub 2.5} implementation strategies.

  16. MOBILE ATMOSPHERIC SENSING

    Directory of Open Access Journals (Sweden)

    L. Wang

    2017-11-01

    Full Text Available Atmospheric quality dramatically deteriorates over the past decades around themetropolitan areas of China. Due to the coal combustion, industrial air pollution, vehicle waste emission, etc., the public health suffers from exposure to such air pollution as fine particles of particulates, sulfur and carbon dioxide, etc. Many meteorological stations have been built to monitor the condition of air quality over the city. However, they are installed at fixed sites and cover quite a small region. The monitoring results of these stations usually do NOT coincide with the public perception of the air quality. This paper is motivated to mimic the human breathing along the citys transportation network by the mobile sensing vehicle of atmospheric quality. To obtain the quantitative perception of air quality, the Environmental Monitoring Vehicle of Wuhan University (EMV-WHU has been developed to automatically collect the data of air pollutants. The EMV-WHU is equipped with GPS/IMU, sensors of PM2.5, carbon dioxide, anemometer, temperature, humidity, noise, and illumination, as well as the visual and infrared camera. All the devices and sensors are well collaborated with the customized synchronization mechanism. Each sort of atmospheric data is accompanied with the uniform spatial and temporal label of high precision. Different spatial and data-mining techniques, such as spatial correlation analysis, logistic regression, spatial clustering, are employed to provide the periodic report of the roadside air quality. With the EMV-WHU, constant collection of the atmospheric data along the Luoyu Road of Wuhan city has been conducted at the daily peak and non-peak time for half a year. Experimental results demonstrated that the EMV is very efficient and accurate for the perception of air quality. Comparative findings with the meteorological stations also show the intelligence of big data analysis and mining of all sorts of EMV measurement of air quality. It is

  17. Sedimentary particulate iron: the missing micronutrients ?

    Science.gov (United States)

    Beghoura, Houda; Gorgues, Thomas; Aumont, Olivier; Planquette, Hélène

    2017-04-01

    Iron is known to regulate the marine primary production and to impact the structure of ecosystems. Indeed, iron is the limiting nutrient for the phytoplankton growth over about 30% of the global ocean. However, the nature of the external sources of iron to the ocean and their quantification remain uncertain. Among these external sources, the sediment sources have been recently shown to be underestimated. Besides, since the operationally defined dissolved iron (which is the sum of truly dissolved and colloidal iron) was traditionally assumed to be the only form available to phytoplankton and bacteria, most studies have focused on the supply of dissolved iron to the ocean, the role of the particulate fraction of iron being largely ignored. This traditional view has been recently challenged, noticeably, by observational evidences. Indeed, in situ observations have shown that large amounts of particulate iron are being resuspended from continental margins to the open ocean thanks to fine grained particles' transport over long distances. A fraction of this particulate iron may dissolve and thereby fuel the phytoplankton growth. The magnitude of the sedimentary sources of particulate iron and the releasing processes affecting this iron phase are not yet well constrained or quantified. As a consequence, the role of sedimentary particulate iron in the biogeochemical cycles is still unclear despite its potentially major widespread importance. Here, we propose a modeling exercise to assess the first order impacts of this newly considered particulate sedimentary iron on global ocean biogeochemistry. We designed global experiments with a coupled dynamical-biogeochemical model (NEMO-PISCES). First, a control simulation that includes only a sediment source of iron in the dissolved phase has been run. Then, this control simulation is being compared with simulations, in which we include a sediment source of iron in both phases (dissolved as well as particulate). Those latter

  18. Development of Polyester/Eggshell Particulate Composites

    OpenAIRE

    S.N. Patrick; V.S. Aigbodion; S.B. Hassan

    2012-01-01

    The development of Polyester/Eggshell particulate composites has been carried out. Uncarbonized and carbonized eggshell particles were used as reinforcement in polyester matrix. 10 to 50 wt% eggshell particles at intervals of 10 wt% were added to polyester as reinforcement. The microstructural analyses of the polyester/eggshell particulate composites were carried out using SEM and EDS. The mechanical properties and density were carried out by standard methods. The results showed that the de...

  19. A large source of dust missing in particulate matter emission inventories? Wind erosion of post-fire landscapes

    Science.gov (United States)

    N. S. Wagenbrenner; S. H. Chung; B. K. Lamb

    2017-01-01

    Wind erosion of soils burned by wildfire contributes substantial particulate matter (PM) in the form of dust to the atmosphere, but the magnitude of this dust source is largely unknown. It is important to accurately quantify dust emissions because they can impact human health, degrade visibility, exacerbate dust-on-snow issues (including snowmelt timing, snow chemistry...

  20. Exposure to atmospheric pms, pahs, pcdd/fs and metals near an open air waste burning site in Beirut

    Directory of Open Access Journals (Sweden)

    Rima Baalbaki

    2016-12-01

    Full Text Available Baalbaki, R., El Hage, R., Nassar, J., Gerard, J., Saliba, N.B., Zaarour, R., Abboud, M., Wehbeh, F., Khalaf, L.K., Shihadeh, A.L., Saliba, N.A. 2016. Exposure to atmospheric PMS, PAHS, PCDD/FS and metals near an open air waste burning site in Beirut. Lebanese Science Journal, 17(2: 91-103. Since July 2015, Lebanon has experienced the worst solid waste management crisis in its history. Consequently, open-air waste burning in the vicinity of highly populated areas in Beirut has become a common practice. This study evaluates the effects of open-air dumping and burning on local air quality and public health. The levels of particulate matter (PM10, PM2.5, gaseous and particle-bound polycyclic aromatic hydrocarbons (PAHs, polychlorinated dibenzo-dioxins and furans (PCDD/Fs, and particle-bound metals at a residence close to waste burning are reported. Concentrations, determined between October 2 and December 2, 2015, were compared either to previous measurements or to measurements taken away from a nearby burning incident, and after it had rained. Subsequently, the cancer risk due to exposure to these chemicals was assessed. Results showed alarming increases in pollutant concentrations which was translated into an increase in short-term cancer risk from about 1 to 20 people per million on the days when waste was being burned. Findings were shared with the public to warn the community against the dangers of waste mismanagement, and underline the obvious need for solid waste management at the governmental and municipal levels.