WorldWideScience

Sample records for oxidants atmospheric concentrations

  1. Nitric oxide concentration measurements in atmospheric pressure flames using electronic-resonance-enhanced coherent anti-Stokes Raman scattering

    Science.gov (United States)

    Chai, N.; Kulatilaka, W. D.; Naik, S. V.; Laurendeau, N. M.; Lucht, R. P.; Kuehner, J. P.; Roy, S.; Katta, V. R.; Gord, J. R.

    2007-06-01

    We report the application of electronic-resonance-enhanced coherent anti-Stokes Raman scattering (ERE-CARS) for measurements of nitric oxide concentration ([NO]) in three different atmospheric pressure flames. Visible pump (532 nm) and Stokes (591 nm) beams are used to probe the Q-branch of the Raman transition. A significant resonance enhancement is obtained by tuning an ultraviolet probe beam (236 nm) into resonance with specific rotational transitions in the (v’=0, v”=1) vibrational band of the A2Σ+-X2Π electronic system of NO. ERE-CARS spectra are recorded at various heights within a hydrogen-air flame producing relatively low concentrations of NO over a Hencken burner. Good agreement is obtained between NO ERE-CARS measurements and the results of flame computations using UNICORN, a two-dimensional flame code. Excellent agreement between measured and calculated NO spectra is also obtained when using a modified version of the Sandia CARSFT code for heavily sooting acetylene-air flames (φ=0.8 to φ=1.6) on the same Hencken burner. Finally, NO concentration profiles are measured using ERE-CARS in a laminar, counter-flow, non-premixed hydrogen-air flame. Spectral scans are recorded by probing the Q1 (9.5), Q1 (13.5) and Q1 (17.5) Raman transitions. The measured shape of the [NO] profile is in good agreement with that predicted using the OPPDIF code, even without correcting for collisional effects. These comparisons between [NO] measurements and predictions establish the utility of ERE-CARS for detection of NO in flames with large temperature and concentration gradients as well as in sooting environments.

  2. Influence of NO2 and metal ions on oxidation of aqueous-phase S(IV in atmospheric concentrations

    Directory of Open Access Journals (Sweden)

    Cláudia R. Martins

    2008-06-01

    Full Text Available An investigation was made of the influence of atmospheric concentrations (15 or 130 ppbv of NO2 on the aqueous-phase oxidation rate of S(IV in the presence and absence of Fe(III, Mn(II and Cr(VI metal ions under controlled experimental conditions (pH, T, concentration of reactants, etc.. The reaction rate in the presence of the NO2 flow was slower than the reaction rate using only clean air with an initial S(IV concentration of 10-4 mol/L. NO2 appears to react with S(IV, producing a kind of inhibitor that slows down the reaction. Conversely, tenfold lower concentrations of S(IV ([S(IV]º = 10-5 mol/L caused a faster reaction in the presence of NO2 than the reaction using purified air. Under these conditions, therefore, the equilibrium shifts to sulfate formation. With the addition of Fe(III, Mn(II or Cr(VI in the presence of a NO2 flow, the reaction occurred faster under all the conditions in which S(IV oxidation was investigated.A reação de oxidação de S(IV em fase aquosa foi estudada em laboratório em presença de NO2 dos íons metálicos Fe(III, Mn(II, e Cr(VI sob condições experimentais controladas (pH, T, concentração dos reagentes, etc.. Na presença de corrente de ar com NO2 (15 ou 130 ppbv a reação de oxidação de S(IV ocorreu mais lentamente do que na presença de ar purificado, para uma concentração inicial de S(IV de 10-4 mol/L. Ao contrário, para concentração inicial de S(IV dez vezes menor ([S(IV]° = 10-5 mol/L a reação ocorreu mais rapidamente na presença de NO2. A explicação está relacionada com o equilíbrio envolvendo a formação de espécies intermediárias de longa vida, que impedem o prosseguimento da reação, porém a depender das concentrações relativas de S(IV e NO2, essas espécies se decompõem deslocando o equilíbrio no sentido de formação de sulfato. A adição dos íons Fe(III, Mn(II ou Cr(VI em presença de corrente de ar com NO2 indicou atividade catalítica para esses íons, em todas

  3. Oxidation of SO2 by stabilized Criegee intermediate (sCI radicals as a crucial source for atmospheric sulfuric acid concentrations

    Directory of Open Access Journals (Sweden)

    M. Boy

    2013-04-01

    Full Text Available The effect of increased reaction rates of stabilized Criegee intermediates (sCIs with SO2 to produce sulfuric acid is investigated using data from two different locations, SMEAR II, Hyytiälä, Finland, and Hohenpeissenberg, Germany. Results from MALTE, a zero-dimensional model, show that using previous values for the rate coefficients of sCI + SO2, the model underestimates gas phase H2SO4 by up to a factor of two when compared to measurements. Using the rate coefficients recently calculated by Mauldin et al. (2012 increases sulfuric acid by 30–40%. Increasing the rate coefficient for formaldehyde oxide (CH2OO with SO2 according to the values recommended by Welz et al. (2012 increases the H2SO4 yield by 3–6%. Taken together, these increases lead to the conclusion that, depending on their concentrations, the reaction of stabilized Criegee intermediates with SO2 could contribute as much as 33–46% to atmospheric sulfuric acid gas phase concentrations at ground level. Using the SMEAR II data, results from SOSA, a one-dimensional model, show that the contribution from sCI reactions to sulfuric acid production is most important in the canopy, where the concentrations of organic compounds are the highest, but can have significant effects on sulfuric acid concentrations up to 100 m. The recent findings that the reaction of sCI + SO2 is much faster than previously thought together with these results show that the inclusion of this new oxidation mechanism could be crucial in regional as well as global models.

  4. Seasonal variation of atmospheric particle number concentrations, new particle formation and atmospheric oxidation capacity at the high Arctic site Villum Research Station, Station Nord

    Directory of Open Access Journals (Sweden)

    Q. T. Nguyen

    2016-09-01

    Full Text Available This work presents an analysis of the physical properties of sub-micrometer aerosol particles measured at the high Arctic site Villum Research Station, Station Nord (VRS, northeast Greenland, between July 2010 and February 2013. The study focuses on particle number concentrations, particle number size distributions and the occurrence of new particle formation (NPF events and their seasonality in the high Arctic, where observations and characterization of such aerosol particle properties and corresponding events are rare and understanding of related processes is lacking.A clear accumulation mode was observed during the darker months from October until mid-May, which became considerably more pronounced during the prominent Arctic haze months from March to mid-May. In contrast, nucleation- and Aitken-mode particles were predominantly observed during the summer months. Analysis of wind direction and wind speed indicated possible contributions of marine sources from the easterly side of the station to the observed summertime particle number concentrations, while southwesterly to westerly winds dominated during the darker months. NPF events lasting from hours to days were mostly observed from June until August, with fewer events observed during the months with less sunlight, i.e., March, April, September and October. The results tend to indicate that ozone (O3 might be weakly anti-correlated with particle number concentrations of the nucleation-mode range (10–30 nm in almost half of the NPF events, while no positive correlation was observed. Calculations of air mass back trajectories using the Hybrid Single Particle Lagrangian Integrated Trajectory (HYSPLIT model for the NPF event days suggested that the onset or interruption of events could possibly be explained by changes in air mass origin. A map of event occurrence probability was computed, indicating that southerly air masses from over the Greenland Sea were more likely linked to those

  5. ISLSCP II Globalview: Atmospheric CO2 Concentrations

    Data.gov (United States)

    National Aeronautics and Space Administration — The GlobalView Carbon Dioxide (CO2) data product contains synchronized and smoothed time series of atmospheric CO2 concentrations at selected sites that were created...

  6. Atmospheric oxidation mechanism of toluene.

    Science.gov (United States)

    Wu, Runrun; Pan, Shanshan; Li, Yun; Wang, Liming

    2014-06-26

    The atmospheric oxidation mechanism of toluene initiated by OH radical addition is investigated by quantum chemistry calculations at M06-2X, G3MP2-RAD, and ROCBS-QB3 levels and by kinetics calculation by using transition state theory and unimolecular reaction theory coupled with master equation (RRKM-ME). The predicted branching ratios are 0.15, 0.59, 0.05, and 0.14 for OH additions to ipso, ortho, meta, and para positions (forming R1-R4 adducts), respectively. The fate of R2, R4, and R1 is investigated in detail. In the atmosphere, R2 reacts with O2 either by irreversible H-abstraction to form o-cresol (36%), or by reversible recombination to R2-1OO-syn and R2-3OO-syn, which subsequently cyclize to bicyclic radical R2-13OO-syn (64%). Similarly, R4 reacts with O2 with branching ratios of 61% for p-cresol and 39% for R4-35OO-syn, while reaction of R1 and O2 leads to R1-26OO-syn. RRKM-ME calculations show that the reactions of R2/R4 with O2 have reached their high-pressure limits at 760 Torr and the formation of R2-16O-3O-s is only important at low pressure, i.e., 5.4% at 100 Torr. The bicyclic radicals (R2-13OO-syn, R4-35OO-syn, and R1-26OO-syn) will recombine with O2 to produce bicyclic alkoxy radicals after reacting with NO. The bicyclic alkoxy radicals would break the ring to form products methylglyoxal/glyoxal (MGLY/GLY) and their corresponding coproducts butenedial/methyl-substituted butenedial as proposed in earlier studies. However, a new reaction pathway is found for the bicyclic alkoxy radicals, leading to products MGLY/GLY and 2,3-epoxybutandial/2-methyl-2,3-epoxybutandial. A new mechanism is proposed for the atmospheric oxidation mechanism of toluene based on current theoretical and previous theoretical and experimental results. The new mechanism predicts much lower yield of GLY and much higher yield of butenedial than other atmospheric models and recent experimental measurements. The new mechanism calls for detection of proposed products 2

  7. Atmospheric Concentrations of Organochlorine Pesticides in the ...

    African Journals Online (AJOL)

    Organochlorine pesticides may still be in use in the Eastern African region for agricultural purposes and for the control of mosquitoes. Atmospheric concentrations of organochlorine pesticides are expected to be higher in the tropics compared to temperate regions due to prevailing high temperatures. However, no study has ...

  8. Study of atmospheric photo-oxidation mechanisms by concentration measurements of peroxy radicals by chemical amplification in the laboratory and in the atmosphere; Etudes des mecanismes de photooxydation atmospherique par mesure des radicaux peroxyles par amplification chimique au laboratoire et dans l'atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Pinceloup, St.

    2002-10-01

    In this thesis, we have continued to develop and to automate a chemical amplifier, with which measurements of peroxy radicals (RO{sub 2}) under real and simulated atmosphere can be made in order to better understand the atmospheric oxidation processes. Firstly, some experiments in laboratory have confirmed the inhibitory effect of water vapour on the chain length of the chemical amplifier, which is a technique of measuring peroxy radicals used by the LCSR. We have shown that the decrease in the chain length is primarily due to the increase of the HO{sub 2} loss to the wall of the amplifier in presence of H2{sub O} and to the HO{sub 2} loss in the gas phase by a minority way of the reaction NO + HO{sub 2} producing HNO{sub 3}. This reaction was studied using a turbulent flow reactor coupled to an ion molecule reactor with mass spectrometric detection. Secondly, the photo-oxidation of formaldehyde has been studied in the atmospheric simulation chamber of the LISA at Creteil coupled with the chemical amplifier. This study has allowed us to determine realistic values of the photolysis constants of radical and molecular ways of formaldehyde and the thermal decomposition constant at 298 K of the adduct HOCH{sub 2}O{sub 2} formed by reaction of HO{sub 2} with HCHO, thanks to the peroxy radicals measurements effectuated. Finally, we have participated in the field campaign, ESCOMPTE, during which concentrations of RO{sub 2}, NO, NO{sub 2} and ozone were measured continuously at the Dupail site. The measured concentrations were typical of a rural site. Using these measurements and those accomplished by other teams, we have determined the production rate of ozone by the radical budget method. The results show that the local photochemical production was important on the Dupail site and controlled essentially by the nitrogen oxides (NO, NO{sub 2}) characterizing a site free of emissions. (author)

  9. The nitrogen oxides and the atmospheric pollution

    International Nuclear Information System (INIS)

    1990-01-01

    The objective of this document is to bring information on the acid atmospheric pollution, on the researches and studies in progress, on the european directives and the national regulations, on the processus and burners with low emission of nitrogen oxides and on the rule that the gas, fuel without sulphur, generating little nitrogen oxides, plays in the fight against atmospheric pollution. 20 refs., 8 figs., 12 tabs

  10. Atmospheric oxidation of selected hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Benter, T.; Olariu, R.I.

    2002-02-01

    This work presents investigations on the gas-phase chemistry of phenol and the cresol isomers performed in a 1080 l quartz glass reactor in Wuppertal and in a large-volume outdoor photoreactor EUPHORE in Valencia, Spain. The studies aimed at clarifying the oxidation mechanisms of the reactions of these compounds with OH and NO{sub 3} radicals. Product investigations on the oxidation of phenol and the cresol isomers initiated by OH radicals were performed in the 1080 l quartz glass reactor with analyses by in situ FT-IR absorption spectroscopy. The primary focus of the investigations was on the determination of product yields. This work represents the first determination and quantification of 1,2-dihydroxybenzenes in the OH oxidation of phenolic compounds. Possible reaction pathways leading to the observed products have been elucidated. (orig.)

  11. Graphite oxidation in HTGR atmosphere

    International Nuclear Information System (INIS)

    Growcock, F.B.; Barry, J.J.; Finfrock, C.C.; Rivera, E.; Heiser, J.H. III

    1982-01-01

    On-going and recently completed studies of the effect of thermal oxidation on the structural integrity of HTGR candidate graphites are described, and some results are presented and discussed. This work includes the study of graphite properties which may play decisive roles in the graphites' resistance to oxidation and fracture: pore size distribution, specific surface area and impurity distribution. Studies of strength loss mechanisms in addition to normal oxidation are described. Emphasis is placed on investigations of the gas permeability of HTGR graphites and the surface burnoff phenomenon observed during recent density profile measurements. The recently completed studies of catalytic pitting and the effects of prestress and stress on reactivity and ultimate strength are also discussed

  12. Atmospheric oxidation of selected alcohols and esters

    Energy Technology Data Exchange (ETDEWEB)

    Becker, K H; Cavalli, F

    2001-03-01

    The decision whether it is appropriate and beneficial for the environment to deploy specific oxygenated organic compounds as replacements for traditional solvent types requires a quantitative assessment of their potential atmospheric impacts including tropospheric ozone and other photooxidant formation. This involves developing chemical mechanisms for the gasphase atmospheric oxidation of the compounds which can be reliably used in models to predict their atmospheric reactivity under a variety of environmental conditions. Until this study, there was very little information available concerning the atmospheric fate of alcohols and esters. The objectives of this study were to measure the atmospheric reaction rates and to define atmospheric reaction mechanisms for the following selected oxygenated volatile organic compounds: the alcohols, 1-butanol and 1-pentanol, and the esters, methyl propionate and dimethyl succinate. The study has successfully addressed these objectives. (orig.)

  13. Greenhouse effect due to atmospheric nitrous oxide

    Science.gov (United States)

    Yung, Y. L.; Wang, W. C.; Lacis, A. A.

    1976-01-01

    The greenhouse effect due to nitrous oxide in the present atmosphere is about 0.8 K. Increase in atmospheric N2O due to perturbation of the nitrogen cycle by man may lead to an increase in surface temperature as large as 0.5 K by 2025, or 1.0 K by 2100. Other climatic effects of N2O are briefly discussed.

  14. Primary atmospheric oxidation mechanism for toluene.

    Science.gov (United States)

    Baltaretu, Cristian O; Lichtman, Eben I; Hadler, Amelia B; Elrod, Matthew J

    2009-01-08

    The products of the primary OH-initiated oxidation of toluene were investigated using the turbulent flow chemical ionization mass spectrometry technique at temperatures ranging from 228 to 298 K. A major dienedial-producing pathway was detected for the first time for toluene oxidation, and glyoxal and methylglyoxal were found to be minor primary oxidation products. The results suggest that secondary oxidation processes involving dienedial and epoxide primary products are likely responsible for previous observations of glyoxal and methylglyoxal products from toluene oxidation. Because the dienedial-producing pathway is a null cycle for tropospheric ozone production and glyoxal and methylglyoxal are important secondary organic aerosol precursors, these new findings have important implications for the modeling of toluene oxidation in the atmosphere.

  15. Reassessing the atmospheric oxidation mechanism of toluene

    Science.gov (United States)

    Ji, Yuemeng; Zhao, Jun; Terazono, Hajime; Misawa, Kentaro; Levitt, Nicholas P.; Li, Yixin; Lin, Yun; Peng, Jianfei; Wang, Yuan; Duan, Lian; Pan, Bowen; Zhang, Fang; Feng, Xidan; An, Taicheng; Marrero-Ortiz, Wilmarie; Secrest, Jeremiah; Zhang, Annie L.; Shibuya, Kazuhiko; Molina, Mario J.; Zhang, Renyi

    2017-08-01

    Photochemical oxidation of aromatic hydrocarbons leads to tropospheric ozone and secondary organic aerosol (SOA) formation, with profound implications for air quality, human health, and climate. Toluene is the most abundant aromatic compound under urban environments, but its detailed chemical oxidation mechanism remains uncertain. From combined laboratory experiments and quantum chemical calculations, we show a toluene oxidation mechanism that is different from the one adopted in current atmospheric models. Our experimental work indicates a larger-than-expected branching ratio for cresols, but a negligible formation of ring-opening products (e.g., methylglyoxal). Quantum chemical calculations also demonstrate that cresols are much more stable than their corresponding peroxy radicals, and, for the most favorable OH (ortho) addition, the pathway of H extraction by O2 to form the cresol proceeds with a smaller barrier than O2 addition to form the peroxy radical. Our results reveal that phenolic (rather than peroxy radical) formation represents the dominant pathway for toluene oxidation, highlighting the necessity to reassess its role in ozone and SOA formation in the atmosphere.

  16. Atmospheric relative concentrations in building wakes

    International Nuclear Information System (INIS)

    Ramsdell, J.V. Jr.; Simonen, C.A.; Smyth, S.B.

    1995-05-01

    This report documents the ARCON95 computer code developed for the U.S. Nuclear Regulatory Commission Office of Nuclear Regulatory Research for use in control room habitability assessments. The document includes a user's guide to the code, a description of the technical basis for the code, and a programmer's guide to the code. The ARCON95 code uses hourly meteorological data and recently developed methods for estimating dispersion in the vicinity of buildings to calculate relative concentrations at control room air intakes that would be exceeded no more five percent of the time. These concentrations are calculated for averaging periods ranging from one hour to 30 days in duration. Relative concentrations calculated by ARCON95 are significantly lower than concentrations calculated using the currently accepted procedure when winds are less than two meters per second. For higher wind speeds, ARCON95 calculates about the same concentrations as the current procedure

  17. Atmospheric Mercury Concentrations Near Salmon Falls Creek Reservoir - Phase 1

    Energy Technology Data Exchange (ETDEWEB)

    M. L. Abbott

    2005-10-01

    Elemental and reactive gaseous mercury (EGM/RGM) were measured in ambient air concentrations over a two-week period in July/August 2005 near Salmon Falls Creek Reservoir, a popular fishery located 50 km southwest of Twin Falls, Idaho. A fish consumption advisory for mercury was posted at the reservoir in 2002 by the Idaho Department of Health and Welfare. The air measurements were part of a multi-media (water, sediment, precipitation, air) study initiated by the Idaho Department of Environmental Quality and the U.S. Environmental Protection Agency (EPA) Region 10 to identify potential sources of mercury contamination to the reservoir. The sampling site is located about 150 km northeast of large gold mining operations in Nevada, which are known to emit large amounts of mercury to the atmosphere (est. 2,200 kg/y from EPA 2003 Toxic Release Inventory). The work was co-funded by the Idaho National Laboratory’s Community Assistance Program and has a secondary objective to better understand mercury inputs to the environment near the INL, which lies approximately 230 km to the northeast. Sampling results showed that both EGM and RGM concentrations were significantly elevated (~ 30 – 70%, P<0.05) compared to known regional background concentrations. Elevated short-term RGM concentrations (the primary form that deposits) were likely due to atmospheric oxidation of high EGM concentrations, which suggests that EGM loading from upwind sources could increase Hg deposition in the area. Back-trajectory analyses indicated that elevated EGM and RGM occurred when air parcels came out of north-central and northeastern Nevada. One EGM peak occurred when the air parcels came out of northwestern Utah. Background concentrations occurred when the air was from upwind locations in Idaho (both northwest and northeast). Based on 2003 EPA Toxic Release Inventory data, it is likely that most of the observed peaks were from Nevada gold mine sources. Emissions from known large natural mercury

  18. Atmospheric relative concentrations in building wakes

    International Nuclear Information System (INIS)

    Ramsdell, J.V. Jr.; Simonen, C.A.

    1997-05-01

    This report documents the ARCON96 computer code developed for the U.S. Nuclear Regulatory Commission Office of Nuclear Reactor Regulation for potential use in control room habitability assessments. It includes a user's guide to the code, a description of the technical basis for the code, and a programmer's guide to the code. The ARCON96 code uses hourly meteorological data and recently developed methods for estimating dispersion in the vicinity of buildings to calculate relative concentrations at control room air intakes that would be exceeded no more than five percent of the time. The concentrations are calculated for averaging periods ranging from one hour to 30 days in duration. ARCON96 is a revised version of ARCON95, which was developed for the NRC Office of Nuclear Regulatory Research. Changes in the code permit users to simulate releases from area sources as well as point sources. The method of averaging concentrations for periods longer than 2 hours has also been changed. The change in averaging procedures increases relative concentrations for these averaging periods. In general, the increase in concentrations is less than a factor of two. The increase is greatest for relatively short averaging periods, for example 0 to 8 hours and diminishes as the duration of the averaging period increases

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

    African Journals Online (AJOL)

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

  20. Greenhouse Gases Concentrations in the Atmosphere Along ...

    African Journals Online (AJOL)

    This study investigated effect of vehicular emission on greenhouse gases concentrations along selected roads of different traffic densities in Abeokuta, Ogun State, Nigeria. Nine roads comprised highway, commercial and residential were selected. Greenhouse Gases (GHGs) were determined from both sides of the roads by ...

  1. Concentrations and fate of decamethylcyclopentasiloxane (D(5)) in the atmosphere.

    Science.gov (United States)

    McLachlan, Michael S; Kierkegaard, Amelie; Hansen, Kaj M; van Egmond, Roger; Christensen, Jesper H; Skjøth, Carsten A

    2010-07-15

    Decamethylcyclopentasiloxane (D(5)) is a volatile compound used in personal care products that is released to the atmosphere in large quantities. Although D(5) is currently under consideration for regulation, there have been no field investigations of its atmospheric fate. We employed a recently developed, quality assured method to measure D(5) concentration in ambient air at a rural site in Sweden. The samples were collected with daily resolution between January and June 2009. The D(5) concentration ranged from 0.3 to 9 ng m(-3), which is 1-3 orders of magnitude lower than previous reports. The measured data were compared with D(5) concentrations predicted using an atmospheric circulation model that included both OH radical and D(5) chemistry. The model was parametrized using emissions estimates and physical chemical properties determined in laboratory experiments. There was good agreement between the measured and modeled D(5) concentrations. The results show that D(5) is clearly subject to long-range atmospheric transport, but that it is also effectively removed from the atmosphere via phototransformation. Atmospheric deposition has little influence on the atmospheric fate. The good agreement between the model predictions and the field observations indicates that there is a good understanding of the major factors governing D(5) concentrations in the atmosphere.

  2. Modeled atmospheric radon concentrations from uranium mines

    Energy Technology Data Exchange (ETDEWEB)

    Droppo, J.G.

    1985-04-01

    Uranium mining and milling operations result in the release of radon from numerous sources of various types and strengths. The US Environmental Protection Agency (EPA) under the Clean Air Act, is assessing the health impact of air emissions of radon from underground uranium mines. In this case, the radon emissions may impact workers and residents in the mine vicinity. To aid in this assessment, the EPA needs to know how mine releases can affect the radon concentrations at populated locations. To obtain this type of information, Pacific Northwest Laboratory used the radon emissions, release characteristics and local meterological conditions for a number of mines to model incremental radon concentrations. Long-term, average, incremental radon concentrations were computed based on the best available information on release rates, plume rise parameters, number and locations of vents, and local dispersion climatology. Calculations are made for a model mine, individual mines, and multiple mines. Our approach was to start with a general case and then consider specific cases for comparison. A model underground uranium mine was used to provide definition of the order of magnitude of typical impacts. Then computations were made for specific mines using the best mine-specific information available for each mine. These case study results are expressed as predicted incremental radon concentration contours plotted on maps with local population data from a previous study. Finally, the effect of possible overlap of radon releases from nearby mines was studied by calculating cumulative radon concentrations for multiple mines in a region with many mines. The dispersion model, modeling assumptions, data sources, computational procedures, and results are documented in this report. 7 refs., 27 figs., 18 tabs.

  3. Modeled atmospheric radon concentrations from uranium mines

    International Nuclear Information System (INIS)

    Droppo, J.G.

    1985-04-01

    Uranium mining and milling operations result in the release of radon from numerous sources of various types and strengths. The US Environmental Protection Agency (EPA) under the Clean Air Act, is assessing the health impact of air emissions of radon from underground uranium mines. In this case, the radon emissions may impact workers and residents in the mine vicinity. To aid in this assessment, the EPA needs to know how mine releases can affect the radon concentrations at populated locations. To obtain this type of information, Pacific Northwest Laboratory used the radon emissions, release characteristics and local meterological conditions for a number of mines to model incremental radon concentrations. Long-term, average, incremental radon concentrations were computed based on the best available information on release rates, plume rise parameters, number and locations of vents, and local dispersion climatology. Calculations are made for a model mine, individual mines, and multiple mines. Our approach was to start with a general case and then consider specific cases for comparison. A model underground uranium mine was used to provide definition of the order of magnitude of typical impacts. Then computations were made for specific mines using the best mine-specific information available for each mine. These case study results are expressed as predicted incremental radon concentration contours plotted on maps with local population data from a previous study. Finally, the effect of possible overlap of radon releases from nearby mines was studied by calculating cumulative radon concentrations for multiple mines in a region with many mines. The dispersion model, modeling assumptions, data sources, computational procedures, and results are documented in this report. 7 refs., 27 figs., 18 tabs

  4. High Performance Nitrous Oxide Analyzer for Atmospheric Research, Phase I

    Data.gov (United States)

    National Aeronautics and Space Administration — This project targets the development of a highly sensitive gas sensor to monitor atmospheric nitrous oxide. Nitrous oxide is an important species in Earth science...

  5. ISLSCP II GlobalView: Atmospheric Methane Concentrations

    Data.gov (United States)

    National Aeronautics and Space Administration — ABSTRACT: The GlobalView Methane (CH4) data product contains synchronized and smoothed time series of atmospheric CH4 concentrations at selected sites that were...

  6. ISLSCP II GlobalView: Atmospheric Methane Concentrations

    Data.gov (United States)

    National Aeronautics and Space Administration — The GlobalView Methane (CH4) data product contains synchronized and smoothed time series of atmospheric CH4 concentrations at selected sites that were created using...

  7. Advances of study on atmospheric methane oxidation (consumption) in forest soil

    Institute of Scientific and Technical Information of China (English)

    WANG Chen-rui; SHI Yi; YANG Xiao-ming; WU Jie; YUE Jin

    2003-01-01

    Next to CO2, methane (CH4) is the second important contributor to global warming in the atmosphere and global atmospheric CH4 budget depends on both CH4 sources and sinks. Unsaturated soil is known as a unique sink for atmospheric CH4 in terrestrial ecosystem. Many comparison studies proved that forest soil had the biggest capacity of oxidizing atmospheric CH4 in various unsaturated soils. However, up to now, there is not an overall review in the aspect of atmospheric CH4 oxidation (consumption) in forest soil. This paper analyzed advances of studies on the mechanism of atmospheric CH4 oxidation, and related natural factors (Soil physical and chemical characters, temperature and moisture, ambient main greenhouse gases concentrations, tree species, and forest fire) and anthropogenic factors (forest clear-cutting and thinning, fertilization, exogenous aluminum salts and atmospheric deposition, adding biocides, and switch of forest land use) in forest soils. It was believed that CH4 consumption rate by forest soil was limited by diffusion and sensitive to changes in water status and temperature of soil. CH4 oxidation was also particularly sensitive to soil C/N, Ambient CO2, CH4 and N2O concentrations, tree species and forest fire. In most cases, anthropogenic disturbances will decrease atmospheric CH4 oxidation, thus resulting in the elevating of atmospheric CH4. Finally, the author pointed out that our knowledge of atmospheric CH4 oxidation (consumption) in forest soil was insufficient. In order to evaluate the contribution of forest soils to atmospheric CH4 oxidation and the role of forest played in the process of global environmental change, and to forecast the trends of global warming exactly, more researchers need to studies further on CH4 oxidation in various forest soils of different areas.

  8. Atmospheric radon daughters concentration inside and outside of cloud

    International Nuclear Information System (INIS)

    Nishikawa, Tsuguo; Okabe, Shigeru; Aoki, Masayoshi; Imamura, Takakazu; Iwata, Yoshitomo; Tamura, Yukihide; Tsuboguchi, Masayasu

    1987-01-01

    The measurements of the atmospheric radon daughters concentration in and out of the cloud were carried out on the top of the mountain, and in the upper air of the sea by using the airplane. The difference of the concentrations between inside and outside of the stratus measured on the top of the mountain was not clear. The atmospheric radon daughters concentration at the top of the mountain decreased when the amount of precipitation at that point was large. Concerning the cumulus investigated by using the airplane, the concentration in the cloud was a little higher than the concentration out of the cloud. Results of the measurements show that the cloud seems to be constructed of the various air masses whose radon daughters concentrations are different from each other even though it appears to be uniform. (author)

  9. Ionization rates and profiles of electron concentration in Martian atmosphere

    International Nuclear Information System (INIS)

    Komitov, B.; Spasov, S.; Gogoshev, M.

    1981-01-01

    The ionization and vertical profiles of electron concentration in the Martian atmosphere are calculated as functions of the solar zenith angles varying from O deg to 90 deg. A neutral atmospheric model based on direct mass-spectometric measurements from the Viking-1 landing modul is employed in the calculation. The Earth data of the ionization solar flux at the same level of the solar activity and for the month of the Viking-1 measurements reduced for the Mars orbit are used. The numerical result for the photoionization rates and quasi-equilibrium electron-concentration profiles in the upper Martian atmosphere at different solar zenith angles from 0 deg to 100 deg are presented. It is shown that the maxima of both quantities decrease and move towards the upper atmosphere regions. The calculated electron density at the zenith solar angle of 40 deg are compared to Viking-1 experimental data and a good agreement is achieved

  10. Trends of atmospheric black carbon concentration over the United Kingdom

    Science.gov (United States)

    Singh, Vikas; Ravindra, Khaiwal; Sahu, Lokesh; Sokhi, Ranjeet

    2018-04-01

    The continuous observations over a period of 7 years (2009-2016) available at 7 locations show declining trend of atmospheric BC in the UK. Among all the locations, the highest decrease of 8 ± 3 percent per year was observed at the Marylebone road in London. The detailed analysis performed at 21 locations during 2009-2011 shows that average annual mean atmospheric BC concentration were 0.45 ± 0.10, 1.47 ± 0.58, 1.34 ± 0.31, 1.83 ± 0.46 and 9.72 ± 0.78 μgm-3 at rural, suburban, urban background, urban centre and kerbside sites respectively. Around 1 μgm-3 of atmospheric BC could be attributed to urban emission, whereas traffic contributed up to 8 μg m-3 of atmospheric BC near busy roads. Seasonal pattern was also observed at all locations except rural and kerbside location, with maximum concentrations (1.2-4 μgm-3) in winter. Further, minimum concentrations (0.3-1.2 μgm-3) were observed in summer and similar concentrations in spring and fall. At suburban and urban background locations, similar diurnal pattern were observed with atmospheric BC concentration peaks (≈1.8 μg m-3) in the morning (around 9 a.m.) and evening (7-9 p.m.) rush hours, whereas minimum concentrations were during late night hours (peak at 5 a.m.) and the afternoon hours (peak at 2 p.m.). The urban centre values show a similar morning pattern (peak at 9 a.m.; concentration - 2.5 μgm-3) in relation to background locations but only a slight decrease in concentration in the afternoon which remained above 2 μgm-3 till midnight. It is concluded that the higher flow of traffic at urban centre locations results in higher atmospheric BC concentrations throughout the day. Comparison of weekday and weekend daily averaged atmospheric BC showed maximum concentrations on Friday, having minimum levels on Sunday. This study will help to refine the atmospheric BC emission inventories and provide data for air pollution and climate change models evaluation, which are used to formulate air pollution

  11. Zirconium oxide obtainment from brazilian zircon concentrate

    International Nuclear Information System (INIS)

    Ribeiro, S.; Martins, A.H.

    1991-01-01

    This work presents the experimental results of studies about alkaline melting, acid leaching and sulfation steps for obtention of zirconium oxide and partially stabilized zirconia by yttrium and rare-earth coprecipitation in chlorine medium, starting from the brazilian zircon concentrate. Using statistical methods of factorial design and the Packett-Burman approach, the results are discussed and the optimal conditions of the production steps were determined. (author)

  12. Pathways for the Oxidation of Sarin in Urban Atmospheres

    Energy Technology Data Exchange (ETDEWEB)

    Gerald E. Streit; James E. Bossert; Jeffrey S. Gaffney; Jon Reisner; Laurie A. McNair; Michael Brown; Scott Elliott

    1998-11-01

    Terrorists have threatened and carried out chemicalhiological agent attacks on targets in major cities. The nerve agent sarin figured prominently in one well-publicized incident. Vapors disseminating from open containers in a Tokyo subway caused thousands of casualties. High-resolution tracer transport modeling of agent dispersion is at hand and will be enhanced by data on reactions with components of the urban atmosphere. As a sample of the level of complexity currently attainable, we elaborate the mechanisms by which sarin can decompose in polluted air. A release scenario is outlined involving the passage of a gas-phase agent through a city locale in the daytime. The atmospheric chemistry database on related organophosphorus pesticides is mined for rate and product information. The hydroxyl,radical and fine-mode particles are identified as major reactants. A review of urban air chernistry/rnicrophysics generates concentration tables for major oxidant and aerosol types in both clean and dirty environments. Organic structure-reactivity relationships yield an upper limit of 10-1' cm3 molecule-' S-* for hydrogen abstraction by hydroxyl. The associated midday loss time scale could be as little as one hour. Product distributions are difficult to define but may include nontoxic organic oxygenates, inorganic phosphorus acids, sarin-like aldehydes, and nitrates preserving cholinergic capabilities. Agent molecules will contact aerosol surfaces in on the order of minutes, with hydrolysis and side-chain oxidation as likely reaction channels.

  13. Studies of atmospheric pollutants concentration factors from La Reina reactor

    International Nuclear Information System (INIS)

    Vera, I.; Alegria, E.

    1983-01-01

    Results of an atmospheric diffusion model for pollutant gases re shown, in which the nuclear reactor of the La Reina Nuclear Centre is considered as the emitting source. The model uses a gaussian shape steady state cloud of concentration of pollutants and actual topographical and meteorological statistics data os the zone. Expected and maximum probable concentration factors are computed in a polar lattice in 16 wind directions. It was found that peaks for expected concentration factors and maximum probable concentration factors at ground level fall within the N and ESE directions at distances where hills or mountains reach the emitted cloud. A discussion of the practical value of these calculations is given. (Author)

  14. Studies of atmospheric pollutants concentration factors from La Reina reactor

    Energy Technology Data Exchange (ETDEWEB)

    Vera, I; Alegria, E [Comision Chilena de Energia Nuclear, Santiago. Div. de Seguridade Nuclear y Radioproteccion

    1983-11-01

    Results of an atmospheric diffusion model for pollutant gases are shown, in which the nuclear reactor of the La Reina Nuclear Centre is considered as the emitting source. The model uses a gaussian shape steady state cloud of concentration of pollutants and actual topographical and meteorological statistics data of the zone. Expected and maximum probable concentration factors are computed in a polar lattice in 16 wind directions. It was found that peaks for expected concentration factors and maximum probable concentration factors at ground level fall within the N and ESE directions at distances where hills or mountains reach the emitted cloud. A discussion of the practical value of these calculations is given.

  15. Oxidation products of biogenic emissions contribute to nucleation of atmospheric particles.

    Science.gov (United States)

    Riccobono, Francesco; Schobesberger, Siegfried; Scott, Catherine E; Dommen, Josef; Ortega, Ismael K; Rondo, Linda; Almeida, João; Amorim, Antonio; Bianchi, Federico; Breitenlechner, Martin; David, André; Downard, Andrew; Dunne, Eimear M; Duplissy, Jonathan; Ehrhart, Sebastian; Flagan, Richard C; Franchin, Alessandro; Hansel, Armin; Junninen, Heikki; Kajos, Maija; Keskinen, Helmi; Kupc, Agnieszka; Kürten, Andreas; Kvashin, Alexander N; Laaksonen, Ari; Lehtipalo, Katrianne; Makhmutov, Vladimir; Mathot, Serge; Nieminen, Tuomo; Onnela, Antti; Petäjä, Tuukka; Praplan, Arnaud P; Santos, Filipe D; Schallhart, Simon; Seinfeld, John H; Sipilä, Mikko; Spracklen, Dominick V; Stozhkov, Yuri; Stratmann, Frank; Tomé, Antonio; Tsagkogeorgas, Georgios; Vaattovaara, Petri; Viisanen, Yrjö; Vrtala, Aron; Wagner, Paul E; Weingartner, Ernest; Wex, Heike; Wimmer, Daniela; Carslaw, Kenneth S; Curtius, Joachim; Donahue, Neil M; Kirkby, Jasper; Kulmala, Markku; Worsnop, Douglas R; Baltensperger, Urs

    2014-05-16

    Atmospheric new-particle formation affects climate and is one of the least understood atmospheric aerosol processes. The complexity and variability of the atmosphere has hindered elucidation of the fundamental mechanism of new-particle formation from gaseous precursors. We show, in experiments performed with the CLOUD (Cosmics Leaving Outdoor Droplets) chamber at CERN, that sulfuric acid and oxidized organic vapors at atmospheric concentrations reproduce particle nucleation rates observed in the lower atmosphere. The experiments reveal a nucleation mechanism involving the formation of clusters containing sulfuric acid and oxidized organic molecules from the very first step. Inclusion of this mechanism in a global aerosol model yields a photochemically and biologically driven seasonal cycle of particle concentrations in the continental boundary layer, in good agreement with observations. Copyright © 2014, American Association for the Advancement of Science.

  16. Oxidation Products of Biogenic Emissions Contribute to Nucleation of Atmospheric Particles

    CERN Document Server

    Riccobono, Francesco; Baltensperger, Urs; Worsnop, Douglas R; Curtius, Joachim; Carslaw, Kenneth S; Wimmer, Daniela; Wex, Heike; Weingartner, Ernest; Wagner, Paul E; Vrtala, Aron; Viisanen, Yrjö; Vaattovaara, Petri; Tsagkogeorgas, Georgios; Tomé, Antonio; Stratmann, Frank; Stozhkov, Yuri; Spracklen, Dominick V; Sipilä, Mikko; Praplan, Arnaud P; Petäjä, Tuukka; Onnela, Antti; Nieminen, Tuomo; Mathot, Serge; Makhmutov, Vladimir; Lehtipalo, Katrianne; Laaksonen, Ari; Kvashin, Alexander N.; Kürten, Andreas; Kupc, Agnieszka; Keskinen, Helmi; Kajos, Maija; Junninen, Heikki; Hansel, Armin; Franchin, Alessandro; Flagan, Richard C; Ehrhart, Sebastian; Duplissy, Jonathan; Dunne, Eimear M; Downard, Andrew; David, André; Breitenlechner, Martin; Bianchi, Federico; Amorim, Antonio; Almeida, João; Rondo, Linda; Ortega, Ismael K; Dommen, Josef; Scott, Catherine E; Vrtala, Aron; Santos, Filipe D; Schallhart, Simon; Seinfeld, John H; Sipila, Mikko; Donahue, Neil M; Kirkby, Jasper; Kulmala, Markku

    2014-01-01

    Atmospheric new-particle formation affects climate and is one of the least understood atmospheric aerosol processes. The complexity and variability of the atmosphere has hindered elucidation of the fundamental mechanism of new-particle formation from gaseous precursors. We show, in experiments performed with the CLOUD (Cosmics Leaving Outdoor Droplets) chamber at CERN, that sulfuric acid and oxidized organic vapors at atmospheric concentrations reproduce particle nucleation rates observed in the lower atmosphere. The experiments reveal a nucleation mechanism involving the formation of clusters containing sulfuric acid and oxidized organic molecules from the very first step. Inclusion of this mechanism in a global aerosol model yields a photochemically and biologically driven seasonal cycle of particle concentrations in the continental boundary layer, in good agreement with observations.

  17. Influence of ship emission on atmospheric pollutant concentration around Osaka Bay, Japan

    International Nuclear Information System (INIS)

    Kondo, A.; Yamaguchi, K.; Nishikawa, E.

    1999-01-01

    Marine traffic in Osaka Bay is very intensified and much atmosphere pollutant (SO x and NO x ) from ships is released but there is no regulation about the ship emission. In this paper, we investigated the emission amounts of SO x NO x and HC from car, factory and ships in Osaka bay area and estimated the influence of the ship emission on the atmospheric pollutant concentration, using both the meteorological prediction model and the atmospheric pollutant concentration prediction model including the dry deposition and the chemical reaction. In Osaka bay area, the emission amounts of SO x and NO x from ships were about 30% of the total emission amounts, respectively. Using these emission data, the atmospheric pollutant concentration was simulated on a summer fine day when high oxidant concentration was measured at several observatories and was compared with the observed data. Though some differences were seen between the simulated results and the observed data, the diurnal variation agreed reasonably. The second simulation was carried out except for the ship emission and we estimated the influence of the ship emission on the atmospheric pollutant concentration. It was found that the ship emission raised SO 2 , NO 2 and NO concentration not only in shore area but also in 40km inland. (Author)

  18. Concentration of elements in atmospheric aerosol in Bratislava

    International Nuclear Information System (INIS)

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

    2006-01-01

    The concentrations of 41 chemical elements (heavy metals, rare earths, and actinides) were determined in atmospheric aerosol using nuclear and related analytical techniques. The sampling location in Bratislava (Slovak Republic). The main goal of this study is the quantification of the atmospheric pollution and its trend. The elemental content in filters was measured using instrumental neutron activation analysis at IBR-2 reactor in JINR Dubna and by atomic absorption spectrometry in Bratislava. The obtained results confirm the decreasing trend of pollution by most of the heavy metals in Bratislava atmosphere, and they are compared with the contents of pollutants in atmosphere of other cities. We determined also the composition of clear filter materials. (Authors)

  19. Denitrification, nitrification, and atmospheric nitrous oxide

    National Research Council Canada - National Science Library

    Delwiche, C. C

    1981-01-01

    In this book, a number of unanswered questions particularly demanding of attention are analyzed to determine the significance of various chemical and biological processes involved with the atmospheric...

  20. Atmospheric tritium concentration in the different chemical forms

    International Nuclear Information System (INIS)

    Akata, Naofumi; Kakiuchi, Hideki; Hisamatsu, Shun'ichi; Shima, Nagayoshi

    2012-01-01

    This study aimed at obtaining background tritium concentrations in air at Rokkasho where the first commercial spent nuclear fuel reprocessing plant in Japan has been under construction. Atmospheric tritium was operationally separated into HTO, HT and hydrocarbon (CH 3 T) fractions, and analyzed for the samples collected every 3 d to 14 d during fiscal year 2005. The HT concentration was the highest among the chemical forms analyzed, followed by the HTO and CH 3 T concentrations. The HT and CH 3 T concentrations did not have clear seasonal variation patterns through the HTO concentrations in spring were higher than those in summer. The HT concentration followed the decline previously reported by Mason and Östlund with an apparent half-life of 4.8 y. The apparent and environmental half-lives of CH 3 T were estimated as 9.2 y and 36.5 y, respectively, by combining the present data with literature data. The Intergovernmental Panel on Climate Change used the atmospheric lifetime of 12 y for CH 4 to estimate global warming in its 2007 report. The longer environmental half-life of CH 3 T suggested its supply from other sources than past nuclear weapon testing in the atmosphere. (author)

  1. 222Rn concentration in the outdoor atmosphere and its relation to the atmospheric stability

    International Nuclear Information System (INIS)

    Holy, K.; Boehm, R.; Bosa, I.; Polaskova, A.; Hola, O.

    1998-01-01

    The radon in the outdoor atmosphere has been monitored continuously since 1991. On the basis of the measured data mainly the average daily and the average annual courses of the 222 Rn concentrations have been studied. The annual courses of 222 Rn concentration are similar for all years. They present the annual variations. The average course of the 222 Rn concentration calculated on the basis of all continual measurements in the years 1991-1997 reaches the maximum value in October and the minimum value in April. The average daily courses of the 222 Rn concentration for the individual months of the year. The average daily courses have a form of waves with a maximum in the morning hours and with a minimum in the afternoon. The maximal amplitudes of daily waves have been reached in the summer months, from June till August. The amplitudes of daily waves are very small at the end of an autumn and during the winter months. The analysis of the daily waves and annual courses of 222 Rn showed that the amplitudes of the daily waves are in proportion to the global solar radiation irradiating the Earth's surface. The day duration influence on the phase of the daily wave and the wind velocity influence mainly on the level of the radon concentration. For the study of the relation of the radon concentration in the outdoor atmosphere to the stability the data of the atmosphere were obtained and they were correlated with the radon concentration. The results indicate that the 222 Rn concentrations int he outdoor atmosphere could be used for determination of the vertical atmospheric stability and these ones could reflect the atmospheric stability more completely than the different classifications based on the knowledge pertinent to the meteorological parameters. (authors)

  2. Atmospheric concentration of 210Pb in East Asia

    International Nuclear Information System (INIS)

    Doi, T.; Sato, S.; Sato, J.

    2003-01-01

    Concentrations of 210 Pb and 7 Be in the surface air were measured at Tsukuba, Japan. The air concentrations of 210 Pb and 7 Be ranged from 0.2 to 0.7 mBq/m 3 and from 1 to 6 mBq/m 3 , respectively. Seasonal variation of 210 Pb concentration was similar to that of 7 Be, showing a 'two-peak' variation pattern: high concentrations appeared in spring and fall. Atmospheric concentrations of 210 Pb and their variations over Urumqi, Lanzhou and Baotou, cities located inland area of the Eurasian Continent, were observed. The monthly average concentrations ranged from 0.27 to 4.57 mBq/m 3 . The concentrations over these cities in winter were several times higher than that observed at Tsukuba, and the range of variation was also larger. The variations in concentration over the 3 localities resembled well with each other, showing the similar seasonal variation pattern: low concentration appeared in summer and high in winter. This variation pattern was different from that observed at Tsukuba. The variations in concentration over the Eurasian Continent, where precipitation is extremely smaller than that of Japan, inversely correlated quite well with the variation in the precipitation. The atmospheric concentrations of 210 Pb ranged from 0.9 to 4.6 mBq/m 3 at Beijing and from 1.4 to 7.8 mBq/m 3 at Chengdu and from 0.5 to 4.9 mBq/m 3 at Seoul, respectively, which were in the similar level to those observed previously in the inland area of the Eurasian Continent. Seasonal variations of the 210 Pb concentration showed the 'one-peak' variation pattern: the maximum levels were recorded in winter season. Small additional rises in the atmospheric 210 Pb concentrations observed in the period from spring to fall seasons may be due to complicated meteorology with high pressure systems at Beijing and Seoul and due to the topographical situation at Chengdu. Long range transport from the Eurasian Continent to the Japanese Islands was also assessed. The air mass from continent reached the

  3. Suspension Hydrogen Reduction of Iron Oxide Concentrates

    Energy Technology Data Exchange (ETDEWEB)

    H.Y. Sohn

    2008-03-31

    The objective of the project is to develop a new ironmaking technology based on hydrogen and fine iron oxide concentrates in a suspension reduction process. The ultimate objective of the new technology is to replace the blast furnace and to drastically reduce CO2 emissions in the steel industry. The goals of this phase of development are; the performance of detailed material and energy balances, thermochemical and equilibrium calculations for sulfur and phosphorus impurities, the determination of the complete kinetics of hydrogen reduction and bench-scale testing of the suspension reduction process using a large laboratory flash reactor.

  4. Reassessing the atmospheric oxidation mechanism of toluene

    OpenAIRE

    Ji, Yuemeng; Zhao, Jun; Terazono, Hajime; Misawa, Kentaro; Levitt, Nicholas P.; Li, Yixin; Lin, Yun; Peng, Jianfei; Wang, Yuan; Duan, Lian; Pan, Bowen; Zhang, Fang; Feng, Xidan; An, Taicheng; Marrero-Ortiz, Wilmarie

    2017-01-01

    Photochemical oxidation of aromatic hydrocarbons leads to tropospheric ozone and secondary organic aerosol (SOA) formation, with profound implications for air quality, human health, and climate. Toluene is the most abundant aromatic compound under urban environments, but its detailed chemical oxidation mechanism remains uncertain. From combined laboratory experiments and quantum chemical calculations, we show a toluene oxidation mechanism that is different from the one adopted in current atmo...

  5. Seasonal variation in diurnal atmospheric grass pollen concentration profiles

    DEFF Research Database (Denmark)

    Peel, Robert George; Ørby, Pia Viuf; Skjøth, Carsten Ambelas

    2014-01-01

    the time of day when peak concentrations are most likely to occur using seasonally averaged diurnal profiles. Atmospheric pollen loads are highly dependent upon emissions, and different species of grass are known to flower and emit pollen at different times of the day and during different periods......In this study, the diurnal atmospheric grass pollen concentration profile within the Danish city of Aarhus was shown to change in a systematic manner as the pollen season progressed. Although diurnal grass pollen profiles can differ greatly from day-to-day, it is common practice to establish...... of the pollen season. Pollen concentrations are also influenced by meteorological factors - directly through those parameters that govern pollen dispersion and transport, and indirectly through the weather-driven flowering process. We found that three different profiles dominated the grass pollen season...

  6. Sintering of dioxide pellets in an oxidizing atmosphere (CO2)

    International Nuclear Information System (INIS)

    Santos, G.R.T.

    1992-01-01

    This work consists in the study of the sintering process of U O 2 pellets in an oxidizing atmosphere. Sintering tests were performed in an CO 2 atmosphere and the influence of temperature and time on the pellets density and microstructure were verified. The results obtained were compared to those from the conventional sintering process and its efficiency was confirmed. (author)

  7. Global atmospheric model for mercury including oxidation by bromine atoms

    Directory of Open Access Journals (Sweden)

    C. D. Holmes

    2010-12-01

    Full Text Available Global models of atmospheric mercury generally assume that gas-phase OH and ozone are the main oxidants converting Hg0 to HgII and thus driving mercury deposition to ecosystems. However, thermodynamic considerations argue against the importance of these reactions. We demonstrate here the viability of atomic bromine (Br as an alternative Hg0 oxidant. We conduct a global 3-D simulation with the GEOS-Chem model assuming gas-phase Br to be the sole Hg0 oxidant (Hg + Br model and compare to the previous version of the model with OH and ozone as the sole oxidants (Hg + OH/O3 model. We specify global 3-D Br concentration fields based on our best understanding of tropospheric and stratospheric Br chemistry. In both the Hg + Br and Hg + OH/O3 models, we add an aqueous photochemical reduction of HgII in cloud to impose a tropospheric lifetime for mercury of 6.5 months against deposition, as needed to reconcile observed total gaseous mercury (TGM concentrations with current estimates of anthropogenic emissions. This added reduction would not be necessary in the Hg + Br model if we adjusted the Br oxidation kinetics downward within their range of uncertainty. We find that the Hg + Br and Hg + OH/O3 models are equally capable of reproducing the spatial distribution of TGM and its seasonal cycle at northern mid-latitudes. The Hg + Br model shows a steeper decline of TGM concentrations from the tropics to southern mid-latitudes. Only the Hg + Br model can reproduce the springtime depletion and summer rebound of TGM observed at polar sites; the snowpack component of GEOS-Chem suggests that 40% of HgII deposited to snow in the Arctic is transferred to the ocean and land reservoirs, amounting to a net deposition flux to the Arctic of 60 Mg a−1. Summertime events of depleted Hg0 at Antarctic sites due to subsidence are much better simulated by

  8. Atmospheric mercury concentrations in the basin of the amazon, Brazil.

    Science.gov (United States)

    Hachiya, N; Takizawa, Y; Hisamatsu, S; Abe, T; Abe, Y; Motohashi, Y

    1998-01-01

    A wide regional mercury pollution in Amazon, Brazil is closely associated with goldmining that has been carried out in the basin of tributaries of the Amazon since the eighteenth century. Possible involvement has been discussed on atmospheric circulation in distributing the volatile pollutant. We developed a portable air sampler for the collection of mercury compounds and determined atmospheric mercury concentrations at several sites in Brazil including the basin of the Amazon tributaries. The mean concentration of total mercury was between 9.1 and 14.0 ng/m(3) in the basin of the Uatumã River located in the tropical rain forest far from goldmining sites and from urbanized area. These mercury levels exceeded the background level previously reported in rural area and, furthermore, were higher than concentrations observed in Rio de Janeiro and in Manaus that were compatible with the reference values for urban area. Mercury concentrations were also determined in gold refineries in the basin of the Tapajos River, and detected at a significant but not a health deteriorating level. Although only preliminary data were available, the present observations were in favor of the hypothesis that mercury is distributed widely by long distant transport by the atmospheric circulation after released at gold mining sites.

  9. Influence of emissions on regional atmospheric mercury concentrations

    Directory of Open Access Journals (Sweden)

    Bieser J.

    2013-04-01

    Full Text Available Mercury is a global pollutant that is rapidly transported in the atmosphere. Unlike the majority of air pollutants the background concentrations of mercury play a major role for the atmospheric concentrations on a hemispheric scale. In this study the influence of regional anthropogenic emissions in comparison to the global emissions on mercury concentrations over Europe are investigated. For this purpose an advanced threedimensional model system is used that consists of three components. The emission model SMOKE-EU, the meteorological model COSMO-CLM, and the chemistry transport model (CTM CMAQ. A variety of sensitivity runs is performed in order to determine the influence of different driving factors (i.e. boundary conditions, anthropogenic and natural emissions, emission factors, meteorological fields on the atmoshperic concentrations of different mercury species. This study is part of the European FP7 project GMOS (Global Mercury Observation System. The aim is to identify the most important drivers for atmospheric mercury in order to optimize future regional modelling studies in the course of the GMOS project. Moreover, the model results are used to determine areas of interest for air-plane based in-situ measurements which are also part of GMOS.

  10. A vegetation control on seasonal variations in global atmospheric mercury concentrations

    Science.gov (United States)

    Jiskra, Martin; Sonke, Jeroen E.; Obrist, Daniel; Bieser, Johannes; Ebinghaus, Ralf; Myhre, Cathrine Lund; Pfaffhuber, Katrine Aspmo; Wängberg, Ingvar; Kyllönen, Katriina; Worthy, Doug; Martin, Lynwill G.; Labuschagne, Casper; Mkololo, Thumeka; Ramonet, Michel; Magand, Olivier; Dommergue, Aurélien

    2018-04-01

    Anthropogenic mercury emissions are transported through the atmosphere as gaseous elemental mercury (Hg(0)) before they are deposited to Earth's surface. Strong seasonality in atmospheric Hg(0) concentrations in the Northern Hemisphere has been explained by two factors: anthropogenic Hg(0) emissions are thought to peak in winter due to higher energy consumption, and atmospheric oxidation rates of Hg(0) are faster in summer. Oxidation-driven Hg(0) seasonality should be equally pronounced in the Southern Hemisphere, which is inconsistent with observations of constant year-round Hg(0) levels. Here, we assess the role of Hg(0) uptake by vegetation as an alternative mechanism for driving Hg(0) seasonality. We find that at terrestrial sites in the Northern Hemisphere, Hg(0) co-varies with CO2, which is known to exhibit a minimum in summer when CO2 is assimilated by vegetation. The amplitude of seasonal oscillations in the atmospheric Hg(0) concentration increases with latitude and is larger at inland terrestrial sites than coastal sites. Using satellite data, we find that the photosynthetic activity of vegetation correlates with Hg(0) levels at individual sites and across continents. We suggest that terrestrial vegetation acts as a global Hg(0) pump, which can contribute to seasonal variations of atmospheric Hg(0), and that decreasing Hg(0) levels in the Northern Hemisphere over the past 20 years can be partly attributed to increased terrestrial net primary production.

  11. Global atmospheric concentrations and source strength of ethane

    Science.gov (United States)

    Blake, D. R.; Rowland, F. S.

    1986-01-01

    A study of the variation in ethane (C2H6) concentration between northern and southern latitudes over three years is presented together with a new estimate of its source strength. Ethane concentrations vary from 0.07 to 2 p.p.b.v. (parts per billion by volume) in air samples collected in remote surface locations in the Pacific (latitude 71 N-47 S) in all four seasons between September 1984 and June 1985. The variations are consistent with southerly transport from sources located chiefly in the Northern Hemisphere, further modified by seasonal variations in the strength of the reaction of C2H6 with OH radicals. These global data can be combined with concurrent data for CH4 and the laboratory reaction rates of each with OH to provide an estimate of three months as the average atmospheric lifetime for C2H6 and 13 + or - 3 Mtons for its annual atmospheric release.

  12. Control of radon and its progeny concentration in indoor atmosphere

    International Nuclear Information System (INIS)

    Ramachandran, T.V.; Subbaramu, M.C.

    1986-01-01

    Exposure to radon daughter concentration in indoor atmosphere can result in a significant risk to the general public. There are two generally used methods for the control of radon and progeny concentration in the indoor atmosphere, namely restriction of radon entry and reduction of indoor radon and its progeny concentration by ventilation or by air cleaning. Predominant radon entry process in most of the dwellings appears to be by pressure driven flow of soil gas through cracks or other openings in the basement slab or subfloors. Sealing these openings or ventilation of the subslab or subfloor space are the methods for reducing the radon entry rates. Indoor radon concentration can also be reduced by increasing the ventilation and by using charcoal filters for the removal of radon gas in indoor air by absorption. Concentration of radon progeny, which are responsible for most of the health risks associatd with radon exposure can also be controlled by the use of electrostatic or mechanical filters. This study describes briefly the above control strategies used for reducing the inhalation doses to persons in dwellings. (author). 9 refs., 2 tables

  13. Effect of Mechanical Alloying Atmospheres and Oxygen Concentration on Mechanical Properties of ODS Ferritic Steels

    International Nuclear Information System (INIS)

    Noh, Sanghoon; Choi, Byoungkwon; Han, Changhee; Kim, Kibaik; Kang, Sukhoon; Chun, Youngbum; Kim, Taekyu

    2013-01-01

    Finely dispersed nano-oxide particles with a high number density in the homogeneous grain matrix are essential to achieve superior mechanical properties at high temperatures, and these unique microstructures can be obtained through the mechanical alloying (MA) and hot consolidation process. The microstructure and mechanical property of ODS steel significantly depends on its powder property and the purity after the MA process. These contents should be carefully controlled to improve the mechanical property at elevated temperature. In particular, appropriate the control of oxygen concentration improves the mechanical property of ODS steel at high temperature. An effective method is to control the mechanical alloying atmosphere by high purity inert gas. In the present study, the effects of mechanical alloying atmospheres and oxygen concentration on the mechanical property of ODS steel were investigated. ODS ferritic alloys were fabricated in various atmospheres, and the HIP process was used to investigate the effects of MA atmospheres and oxygen concentration on the microstructure and mechanical property. ODS ferritic alloys milled in an Ar-H 2 mixture, and He is effective to reduce the excess oxygen concentration. The YH 2 addition made an extremely reduced oxygen concentration by the internal oxygen reduction reaction and resulted in a homogeneous microstructure and superior creep strength

  14. Atmospheric Oxidation Mechanism of Furfural Initiated by Hydroxyl Radicals.

    Science.gov (United States)

    Zhao, Xiaocan; Wang, Liming

    2017-05-04

    Furfural is emitted into the atmosphere because of its potential applications as an intermediate to alkane fuels from biomass, industrial usages, and biomass burning. The kinetic and mechanistic information on the furfural chemistry is necessary to assess the fate of furfural in the atmosphere and its impact on the air quality. Here we studied the atmospheric oxidation mechanisms of furfural initiated by the OH radicals using quantum chemistry and kinetic calculations. The reaction of OH and furfural was initiated mainly by OH additions to C 2 and C 5 positions, forming R2 and R5 adducts, which could undergo rapid ring-breakage to form R2B and R5B, respectively. Our calculations showed that these intermediate radicals reacted rather slowly with O 2 under the atmospheric conditions because the additions of O 2 to these radicals are only slightly exothermic and highly reversible. Alternatively, these radicals would react directly with O 3 , NO 2 , HO 2 /RO 2 , etc. Namely, the atmospheric oxidation of furfural would unlikely result in ozone formation. Under typical atmospheric conditions, the main products in OH-initiated furfural oxidation include 2-oxo-3-pentene-1,5-dialdehyde, 5-hydroxy-2(5H)-furanone, 4-oxo-2- butenoic acid, and 2,5-furandione. These compounds will likely stay in the gas phase and are subject to further photo-oxidation.

  15. HO2 measurements at atmospheric concentrations using a chemical ionization mass spectrometry

    Science.gov (United States)

    Albrecht, S.; Novelli, A.; Hofzumahaus, A.; Kang, S.; Baker, Y.; Mentel, T. F.; Fuchs, H.

    2017-12-01

    Correct and precise measurements of atmospheric radical species are necessary for a better understanding of the oxidative capacity of the atmosphere. Due to the reactivity of radicals, and their consequent low concentrations, direct measurements of these species are particularly challenging and have been proven in the past to be affected by interfering species. Here we present a chemical ionization source coupled to an APi-HR-TOF-MS (Aerodyne Research Inc.), which has a limit of detection for HO2 radicals well below its atmospheric concentrations ( 1 x 108 molecules cm-3). The instrument was calibrated with a well-established and characterized HO2 calibration source in use for the laser induced fluorescence instrument in the Forschungszentrum Jülich. Within the source, a well characterized amount of HO2 radicals is produced after photolysis of water by a mercury lamp. In addition, several experiments were performed in the atmosphere simulation chamber SAPHIR at the Forschungszentrum Jülich to test for potential interferences. Measurements of HO2 radicals were concurrently detected by a laser induced fluorescence instrument allowing for the comparison of measurements within the two different and independent techniques for various atmospheric conditions regarding concentrations of O3, NOx and VOCs. Results from the intercomparison together with the calibration procedure of the instrument and laboratory characterization will be presented.

  16. Effectiveness of Emission Controls to Reduce the Atmospheric Concentrations of Mercury.

    Science.gov (United States)

    Castro, Mark S; Sherwell, John

    2015-12-15

    Coal-fired power plants in the United States are required to reduce their emissions of mercury (Hg) into the atmosphere to lower the exposure of Hg to humans. The effectiveness of power-plant emission controls on the atmospheric concentrations of Hg in the United States is largely unknown because there are few long-term high-quality atmospheric Hg data sets. Here, we present the atmospheric concentrations of Hg and sulfur dioxide (SO2) measured from 2006 to 2015 at a relatively pristine location in western Maryland that is several (>50 km) kilometers downwind of power plants in Ohio, Pennsylvania, and West Virginia. Annual average atmospheric concentrations of gaseous oxidized mercury (GOM), SO2, fine particulate mercury (PBM2.5), and gaseous elemental mercury (GEM) declined by 75%, 75%, 43%, and 13%, respectively, and were strongly correlated with power-plant Hg emissions from the upwind states. These results provide compelling evidence that reductions in Hg emissions from power plants in the United States had their intended impact to reduce regional Hg pollution.

  17. Conventional methanotrophs are responsible for atmospheric methane oxidation in paddy soils

    NARCIS (Netherlands)

    Cai, Yuanfeng; Yan, Zheng; Bodelier, P.L.E.; Conrad, R.; Jia, Zhongjun

    2016-01-01

    Soils serve as the biological sink of the potent greenhouse gas methane with exceptionally low concentrations of ~1.84 p.p.m.v. in the atmosphere. The as-yet-uncultivated methane-consuming bacteria have long been proposed to be responsible for this ‘high-affinity’ methane oxidation (HAMO). Here we

  18. Size-resolved mass concentrations of iron oxide aerosols and size-resolved number concentrations of iron oxide aerosols collected from King Air aircraft in Yellow Sea and East China Sea from 2013-02-14 to 2013-03-10 (NCEI Accession 0162201)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — This dataset contains size-resolved mass concentrations of iron oxide aerosols and size-resolved number concentrations of iron oxide aerosols, measured using the...

  19. Valence control of cobalt oxide thin films by annealing atmosphere

    International Nuclear Information System (INIS)

    Wang Shijing; Zhang Boping; Zhao Cuihua; Li Songjie; Zhang Meixia; Yan Liping

    2011-01-01

    The cobalt oxide (CoO and Co 3 O 4 ) thin films were successfully prepared using a spin-coating technique by a chemical solution method with CH 3 OCH 2 CH 2 OH and Co(NO 3 ) 2 .6H 2 O as starting materials. The grayish cobalt oxide films had uniform crystalline grains with less than 50 nm in diameter. The phase structure is able to tailor by controlling the annealing atmosphere and temperature, in which Co 3 O 4 thin film was obtained by annealing in air at 300-600, and N 2 at 300, and transferred to CoO thin film by raising annealing temperature in N 2 . The fitted X-ray photoelectron spectroscopy (XPS) spectra of the Co2p electrons are distinguishable from different valence states of cobalt oxide especially for their satellite structure. The valence control of cobalt oxide thin films by annealing atmosphere contributes to the tailored optical absorption property.

  20. Atmospheric oxygen regulation at low Proterozoic levels by incomplete oxidative weathering of sedimentary organic carbon

    Science.gov (United States)

    Daines, Stuart J.; Mills, Benjamin J. W.; Lenton, Timothy M.

    2017-02-01

    It is unclear why atmospheric oxygen remained trapped at low levels for more than 1.5 billion years following the Paleoproterozoic Great Oxidation Event. Here, we use models for erosion, weathering and biogeochemical cycling to show that this can be explained by the tectonic recycling of previously accumulated sedimentary organic carbon, combined with the oxygen sensitivity of oxidative weathering. Our results indicate a strong negative feedback regime when atmospheric oxygen concentration is of order pO2~0.1 PAL (present atmospheric level), but that stability is lost at pO2counterbalancing changes in the weathering of isotopically light organic carbon. This can explain the lack of secular trend in the Precambrian δ13C record, and reopens the possibility that increased biological productivity and resultant organic carbon burial drove the Great Oxidation Event.

  1. High-Temperature, Dual-Atmosphere Corrosion of Solid-Oxide Fuel Cell Interconnects

    Science.gov (United States)

    Gannon, Paul; Amendola, Roberta

    2012-12-01

    High-temperature corrosion of ferritic stainless steel (FSS) surfaces can be accelerated and anomalous when it is simultaneously subjected to different gaseous environments, e.g., when separating fuel (hydrogen) and oxidant (air) streams, in comparison with single-atmosphere exposures, e.g., air only. This so-called "dual-atmosphere" exposure is realized in many energy-conversion systems including turbines, boilers, gasifiers, heat exchangers, and particularly in intermediate temperature (600-800°C) planar solid-oxide fuel cell (SOFC) stacks. It is generally accepted that hydrogen transport through the FSS (plate or tube) and its subsequent integration into the growing air-side surface oxide layer can promote accelerated and anomalous corrosion—relative to single-atmosphere exposure—via defect chemistry changes, such as increased cation vacancy concentrations, decreased oxygen activity, and steam formation within the growing surface oxide layers. Establishment of a continuous and dense surface oxide layer on the fuel side of the FSS can inhibit hydrogen transport and the associated effects on the air side. Minor differences in FSS composition, microstructure, and surface conditions can all have dramatic influences on dual-atmosphere corrosion behaviors. This article reviews high-temperature, dual-atmosphere corrosion phenomena and discusses implications for SOFC stacks, related applications, and future research.

  2. Source contributions to atmospheric fine carbon particle concentrations

    Science.gov (United States)

    Andrew Gray, H.; Cass, Glen R.

    A Lagrangian particle-in-cell air quality model has been developed that facilitates the study of source contributions to atmospheric fine elemental carbon and fine primary total carbon particle concentrations. Model performance was tested using spatially and temporally resolved emissions and air quality data gathered for this purpose in the Los Angeles area for the year 1982. It was shown that black elemental carbon (EC) particle concentrations in that city were dominated by emissions from diesel engines including both on-highway and off-highway applications. Fine primary total carbon particle concentrations (TC=EC+organic carbon) resulted from the accumulation of small increments from a great variety of emission source types including both gasoline and diesel powered highway vehicles, stationary source fuel oil and gas combustion, industrial processes, paved road dust, fireplaces, cigarettes and food cooking (e.g. charbroilers). Strategies for black elemental carbon particle concentration control will of necessity need to focus on diesel engines, while controls directed at total carbon particle concentrations will have to be diversified over a great many source types.

  3. The measurement of airborne rodon daughter concentrations in the atmosphere

    International Nuclear Information System (INIS)

    Ha, C.W.; Lee, J.K.; Moon, P.S.

    1979-01-01

    A simple method for determining the airborne concentration of radon daughter products has been developed, which is based on gross alpha counting of the air filter collections at several time intervals after completion of air sampling. The concentration of each nuclide is then obtained from an equation involving the alpha disintegrations, the sampling time, and the known numerical coefficients. The state of radioactive disequilibrium is also inventigated. The atmosphere sampled in the TRIGA Mark-III reactor room was largely in disequilibrium. The extent of radioactive disequilibrium between radon daughter products seems likely depend on sampling times associated with turbulence conditions. The data obtained here will certainly provide useful information on the evaluation of internal exposure and calibration of effluent monitoring instruments. (author)

  4. Monitoring of mercury concentration in atmosphere in Usti nad Labem

    International Nuclear Information System (INIS)

    Synek, V.; Baloch, T.; Otcenasek, J.; Kremlova, S.; Subrt, P.

    2007-01-01

    This study elaborates the observation of mercury pollution of the atmosphere in the city of Usti nad Labem. The biggest source of the polluting mercury in Usti nad Labem is the chlor-alkali production in the factory of Spolchemie Inc. The method of mercury determination applied is based on capturing the mercury contented in a volume of the air on an amalgamator and measuring the mercury by an atomic absorption spectrometer (Perkin -Elmer 4100ZL) equipped with a special adapter after a thermal release of the mercury from the amalgamator. The basic characteristics of this method were evaluated; e.g. the limit of detection and limit of determination are, respectively, 0.43 and 1.4 ng/m 3 , the relative expanded uncertainty is 28 %. The work gives results of long-term (1998-2006) observations in a few localities in Usti nad Labem situated in various distances from the mercury source (e.g. means of 28.6 and 14.1 ng/m3 were obtained, respectively, in places 350 and 700 m far from the electrolysis plant) and also in a different city (Duchcov). The cases with a higher mercury concentration are very frequent so the sets of the obtained results have lognormal distributions. This study statistically compares the total level and variability of the mercury concentrations in the time series. It also investigates their trends, correlations between them and meteorological influences upon the levels of mercury concentration in the air. The effect of the mercury emission from the chlor-alkali plant is dominant. It as the only factor determines when the cases with a high mercury concentration in the atmosphere occur. (author)

  5. Effect of high-oxygen atmosphere packaging on oxidative stability and sensory quality of two chicken muscles during chill storage

    DEFF Research Database (Denmark)

    Jongberg, Sisse; Wen, Jinzhu; Tørngren, Mari Ann

    2014-01-01

    The oxidative stability and sensory quality of chicken breast (m. pectoralis) and thigh (m. peroneus longus) stored in high-oxygen modified atmosphere (MAP-O), non-oxygen modified atmosphere (MAP-N), or vacuum for up to 9 days at 5°C were investigated. Protein thiol concentration in breasts and t...

  6. Continuous determination of nitric oxide and nitrogen dioxide in the atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Yanagisawa, S; Yamate, N; Mitsuzawa, S; Mori, M

    1966-10-01

    Continuous determinations of nitric oxide and nitrogen dioxide in that atmospheric air by the use of a modified Saltzman reagent is described. Measurement was made intermittently, once every 30 min., by an automatic continuous analyzer equipped with a single-path colorimeter. The response of the analyzer was obtained as an average of the concentration of nitrogen oxides over a period of 25 min. Two bubblers were used for absorbing nitrogen oxides into the modified Saltzman reagent, whose transmittance was measured for the determination. One bubbler was designed to absorb nitrogen dioxide, and the other, nitric oxide plus nitrogen dioxide after the oxidation of the nitric oxide by permanganate. The oxidizing efficiency of the permanganate was 96-100%. The acetic acid in the Saltzman reagent was replaced with n-propyl alcohol in the modified Saltzman reagent; the spontaneous coloration and corrosive quality of the reagent was decreased by this substitution. The concentration of nitric oxide was obtained from the difference between the two responses of the analyzer, while the concentration of nitrogen dioxide could be read directly from the indication of the recorder. The transmittance ratio method was applied to the measurements, accurate determinations were possible, even at high blank values. Therefore, the reagent was used repeatedly by cycling it on the basis of measuring the difference in the coloration of the reagent before and after the absorption of nitrogen oxides. The analyzer could be used for a long period without changing the reagent.

  7. The role and importance of ozone for atmospheric chemistry and methods for measuring its concentration

    Directory of Open Access Journals (Sweden)

    Marković Dragan M.

    2003-01-01

    Full Text Available Depending on where ozone resides, it can protect or harm life on Earth. The thin layer of ozone that surrounds Earth acts as a shield protecting the planet from irradiation by UV light. When it is close to the planet's surface, ozone is a powerful photochemical oxidant that damage, icons frescos, museum exhibits, rubber, plastic and all plant and animal life. Besides the basic properties of some methods for determining the ozone concentration in working and living conditions, this paper presents a detailed description of the electrochemical method. The basic properties of the electrochemical method are used in the construction of mobile equipment for determining the sum of oxidants in the atmosphere. The equipment was used for testing the determination of the ozone concentration in working rooms, where the concentration was at a high level and caused by UV radiation or electrostatic discharge. According to the obtained results, it can be concluded that this equipment for determining the ozone concentration in the atmosphere is very powerful and reproducible in measurements.

  8. Elevated atmospheric carbon dioxide concentrations promote ant tending of aphids.

    Science.gov (United States)

    Kremer, Jenni M M; Nooten, Sabine S; Cook, James M; Ryalls, James M W; Barton, Craig V M; Johnson, Scott N

    2018-04-27

    Animal mutualisms, which involve beneficial interactions between individuals of different species, are common in nature. Insect-insect mutualism, for example, is widely regarded as a keystone ecological interaction. Some mutualisms are anticipated to be modified by climate change, but the focus has largely been on plant-microbe and plant-animal mutualisms rather than those between animals. Ant-aphid mutualisms, whereby ants tend aphids to harvest their honeydew excretions and, in return, provide protection for the aphids, are widespread. The mutualism is heavily influenced by the quality and quantity of honeydew produced by aphids, which is directly affected by host plant quality. As predicted increases in concentrations of atmospheric carbon dioxide (eCO 2 ) are widely reported to affect plant nutritional chemistry, this may also alter honeydew quality and hence the nature of ant-aphid mutualisms. Using glasshouse chambers and field-based open-top chambers, we determined the effect of eCO 2 on the growth and nutritional quality (foliar amino acids) of lucerne (Medicago sativa). We determined how cowpea aphid (Aphis craccivora) populations and honeydew production were impacted when feeding on such plants and how this affected the tending behaviour of ants (Iridomyrmex sp.). eCO 2 stimulated plant growth but decreased concentrations of foliar amino acids by 29% and 14% on aphid-infested plants and aphid-free plants, respectively. Despite the deterioration in host plant quality under eCO 2 , aphids maintained performance and populations were unchanged by eCO 2 . Aphids induced higher concentrations of amino acids (glutamine, asparagine, glutamic acid and aspartic acid) important for endosymbiont-mediated synthesis of essential amino acids. Aphids feeding under eCO 2 also produced over three times more honeydew than aphids feeding under ambient CO 2 , suggesting they were imbibing more phloem sap at eCO 2 . The frequency of ant tending of aphids more than doubled in

  9. Atmospheric conditions during high ragweed pollen concentrations in Zagreb, Croatia

    Science.gov (United States)

    Prtenjak, Maja Telišman; Srnec, Lidija; Peternel, Renata; Madžarević, Valentina; Hrga, Ivana; Stjepanović, Barbara

    2012-11-01

    We examined the atmospheric conditions favourable to the occurrence of maximum concentrations of ragweed pollen with an extremely high risk of producing allergy. Over the 2002-2009 period, daily pollen data collected in Zagreb were used to identify two periods of high pollen concentration (> 600 grains/m3) for our analysis: period A (3-4 September 2002) and period B (6-7 September 2003). Synoptic conditions in both periods were very similar: Croatia was under the influence of a lower sector high pressure system moving slowly eastward over Eastern Europe. During the 2002-2009 period, this type of weather pattern (on ~ 70% of days), in conjunction with almost non-gradient surface pressure conditions in the area (on ~ 30% of days) characterised days when the daily pollen concentrations were higher than 400 grains/m3. Numerical experiments using a mesoscale model at fine resolution showed successful multi-day simulations reproducing the local topographic influence on wind flow and in reasonable agreement with available observations. According to the model, the relatively weak synoptic flow (predominantly from the eastern direction) allowed local thermal circulations to develop over Zagreb during both high pollen episodes. Two-hour pollen concentrations and 48-h back-trajectories indicated that regional-range transport of pollen grains from the central Pannonian Plain was the cause of the high pollen concentrations during period A. During period B, the north-westward regional-range transport in Zagreb was supplemented significantly by pronounced horizontal recirculation of pollen grains. This recirculation happened within the diurnal local circulation over the city, causing a late-evening increase in pollen concentration.

  10. Climatology of atmospheric PM10 concentration in the Po Valley

    Science.gov (United States)

    Bigi, A.; Ghermandi, G.

    2014-01-01

    The limits to atmospheric pollutant concentration set by the European Commission provide a challenging target for the municipalities in the Po Valley, because of the characteristic climatic conditions and high population density of this region. In order to assess climatology and trends in the concentration of atmospheric particles in the Po Valley, a dataset of PM10 data from 41 sites across the Po Valley have been analysed, including both traffic and background sites (either urban, suburban or rural). Of these 41 sites, 18 with 10 yr or longer record have been analysed for long term trend in de-seasonalized monthly means, in annual quantiles and in monthly frequency distribution. A widespread significant decreasing trend has been observed at most sites, up to few percent per year, by Generalised Least Square and Theil-Sen method. All 41 sites have been tested for significant weekly periodicity by Kruskal-Wallis test for mean anomalies and by Wilcoxon test for weekend effect magnitude. A significant weekly periodicity has been observed for most PM10 series, particularly in summer and ascribed mainly to anthropic particulate emissions. A cluster analysis has been applied in order to highlight stations sharing similar pollution conditions over the reference period. Five clusters have been found, two gathering the metropolitan areas of Torino and Milano and their respective nearby sites and the other three clusters gathering north-east, north-west and central Po Valley sites respectively. Finally the observed trends in atmospheric PM10 have been compared to trends in provincial emissions of particulates and PM precursors, and analysed along with data on vehicular fleet age, composition and fuel sales. Significant basin-wide drop in emissions occurred for gaseous pollutants, contrarily to emissions of PM10 and PM2.5, whose drop resulted low and restricted to few provinces. It is not clear whether the decrease for only gaseous emissions is sufficient to explain the

  11. Organic Nitrogen in Atmospheric Drops and Particles: Concentrations, (Limited) Speciation, and Chemical Transformations

    Science.gov (United States)

    Anastasio, C.; Zhang, Q.

    2003-12-01

    While quite a bit is known of the concentrations, speciation, and chemistry of inorganic forms of nitrogen in the atmosphere, the same cannot be said for organic forms. Despite this, there is growing evidence that organic N (ON) is ubiquitous in the atmosphere, especially in atmospheric condensed phases such as fog/cloud drops and aerosol particles. Although the major compounds that make up organic N are generally unknown, as are the sources of these compounds, it is clear that there are significant fluxes of ON between the atmosphere and ecosystems. It also appears that organic N can have significant effects in both spheres. The goal of our recent work in this area has been to better describe the atmospheric component of the biogeochemistry of organic nitrogen. Based on particle, gas, and fogwater samples from Northern California we have made three major findings: 1) Organic N represents a significant component, approximately 20%, of the total atmospheric N loading in these samples. This is broadly consistent with studies from other locations. 2) Amino compounds, primarily as combined amino acids, account for approximately 20% of the measured ON in our condensed phase samples. Given the properties of amino acids, these compounds could significantly affect the chemical and physical properties of atmospheric particles. 3) Organic nitrogen in atmospheric particles and drops is transformed to inorganic forms - primarily ammonium, nitrate, and nitrogen oxides (NOx) - during exposure to sunlight and/or ozone. These chemical reactions likely increase the bioavailability of the condensed phase nitrogen pool and enhance its biological effects after deposition to ecosystems.

  12. Determination of atmospheric concentrations of xenon radioisotopes. Progress report

    International Nuclear Information System (INIS)

    Abel, K.H.; Panisko, M.E.; Hensley, W.K.; Bowyer, T.W.; Perkins, R.W.

    1995-07-01

    Determination of radioactive xenon concentrations in the atmosphere over a two year period has been performed as part of a research program to develop real-time measurement capabilities. The initial measurements were made to develop, prove, and validate the authors technical approach, while the longer-term measurements are being undertaken to establish natural background concentrations and variability with time. The results reported were made using noble gas fraction (typically 90% Kr and 10% Xe by weight) gas samples obtained from a commercial air-reduction plant in the northeastern US over a two-year interval beginning in the fall of 1993. The concentrated gas samples were typically obtained during a 6--8 hour interval at the commercial reduction plant and were shipped overnight to their laboratory. Analysis was typically completed approximately 24 hours after sampling. The analytical separation process typically took approximately 6 hours and gamma-ray spectrometric measurements were conducted for intervals ranging from 3 to 16 hours. The technical approach involved removal of potentially interfering radon daughter radionuclides using a molecular sieve at room temperature, followed by cryogenic concentration of noble gases using a chilled (-76 C) activated carbon molecular sieve. During initial measurements both molecular sieve materials were contained in 30 foot x 1/4 inch gas chromatography columns for analytical separations. Krypton was separated from Xenon during the analytical procedure by warming the activated carbon molecular sieve to room temperature after initial noble gas concentration and actively pumping it away. Xenon-133 adsorbed to the activated charcoal molecular sieve was then quantified via its 81 keV gamma-ray using initially a p-type intrinsic germanium detector and later a higher efficiency (64% relative to a 3 inch x 3 inch sodium iodide) n-type intrinsic germanium detector

  13. Interlaboratory model comparisons of atmospheric concentrations with and without deposition

    International Nuclear Information System (INIS)

    Kern, C.D.; Cooper, R.E.

    1978-01-01

    To calculate the dose to the regional and U.S. populations, the pollutant concentration both with and without deposition and the amount of material deposited on the ground and watersheds around such a facility must be known. The following report (Article 50) of this document contains some initial estimates of population exposure from atmospheric effluents. The expertise of laboratories supported by U.S. Department of Energy funds ensures that the latest methods and data are available. Lawrence Livermore Laboratory (LLL) performed regional calculations (out to distances of the order of 200 km from a hypothetical fuel reprocessing plant). The Air Resources Laboratory (ARL) of the National Oceanic and Atmospheric Administration (NOAA), and Battelle Pacific Northwest Laboratories (PNL) performed U.S. scale calculations, and ARL also did the global calculations. Data from a winter and summer period were used to make comparisons of calculations by LLL, ARL, and PNL to determine which model should be used for the final calculations and to determine if a 200-km square area centered on the site would be large enough for dose calculations via the water and food pathways

  14. Growth under elevated atmospheric CO(2) concentration accelerates leaf senescence in sunflower (Helianthus annuus L.) plants.

    Science.gov (United States)

    de la Mata, Lourdes; Cabello, Purificación; de la Haba, Purificación; Agüera, Eloísa

    2012-09-15

    Some morphogenetic and metabolic processes were sensitive to a high atmospheric CO(2) concentration during sunflower primary leaf ontogeny. Young leaves of sunflower plants growing under elevated CO(2) concentration exhibited increased growth, as reflected by the high specific leaf mass referred to as dry weight in young leaves (16 days). The content of photosynthetic pigments decreased with leaf development, especially in plants grown under elevated CO(2) concentrations, suggesting that high CO(2) accelerates chlorophyll degradation, and also possibly leaf senescence. Elevated CO(2) concentration increased the oxidative stress in sunflower plants by increasing H(2)O(2) levels and decreasing activity of antioxidant enzymes such as catalase and ascorbate peroxidase. The loss of plant defenses probably increases the concentration of reactive oxygen species in the chloroplast, decreasing the photosynthetic pigment content as a result. Elevated CO(2) concentration was found to boost photosynthetic CO(2) fixation, especially in young leaves. High CO(2) also increased the starch and soluble sugar contents (glucose and fructose) and the C/N ratio during sunflower primary leaf development. At the beginning of senescence, we observed a strong increase in the hexoses to sucrose ratio that was especially marked at high CO(2) concentration. These results indicate that elevated CO(2) concentration could promote leaf senescence in sunflower plants by affecting the soluble sugar levels, the C/N ratio and the oxidative status during leaf ontogeny. It is likely that systemic signals produced in plants grown with elevated CO(2), lead to early senescence and a higher oxidation state of the cells of these plant leaves. Copyright © 2012 Elsevier GmbH. All rights reserved.

  15. Deep Sea Memory of High Atmospheric CO2 Concentration

    Science.gov (United States)

    Mathesius, Sabine; Hofmann, Matthias; Caldeira, Ken; Schellnhuber, Hans Joachim

    2015-04-01

    Carbon dioxide removal (CDR) from the atmosphere has been proposed as a powerful measure to mitigate global warming and ocean acidification. Planetary-scale interventions of that kind are often portrayed as "last-resort strategies", which need to weigh in if humankind keeps on enhancing the climate-system stock of CO2. Yet even if CDR could restore atmospheric CO2 to substantially lower concentrations, would it really qualify to undo the critical impacts of past emissions? In the study presented here, we employed an Earth System Model of Intermediate Complexity (EMIC) to investigate how CDR might erase the emissions legacy in the marine environment, focusing on pH, temperature and dissolved oxygen. Against a background of a world following the RCP8.5 emissions path ("business-as-usual") for centuries, we simulated the effects of two massive CDR interventions with CO2 extraction rates of 5 GtC yr-1 and 25 GtC yr-1, respectively, starting in 2250. We found that the 5 GtC yr-1 scheme would have only minor ameliorative influence on the oceans, even after several centuries of application. By way of contrast, the extreme 25 GtC yr-1 scheme eventually leads to tangible improvements. However, even with such an aggressive measure, past CO2 emissions leave a substantial legacy in the marine environment within the simulated period (i.e., until 2700). In summary, our study demonstrates that anthropogenic alterations of the oceans, caused by continued business-as-usual emissions, may not be reversed on a multi-centennial time scale by the most aspirational geoengineering measures. We also found that a transition from the RCP8.5 state to the state of a strong mitigation scenario (RCP2.6) is not possible, even under the assumption of extreme extraction rates (25 GtC yr-1). This is explicitly demonstrated by simulating additional scenarios, starting CDR already in 2150 and operating until the atmospheric CO2 concentration reaches 280 ppm and 180 ppm, respectively. The simulated

  16. NITROUS OXIDE CONCENTRATIONS IN SMALL STREAMS OF THE GEORGIA PIEDMONT

    Science.gov (United States)

    We are measuring the dissolved nitrous oxide concentration in 17 headwater streams in the South Fork Broad River, Georgia watershed on a monthly basis. The selected small streams drain watersheds dominated by forest, pasture, developed, or mixed land uses. Nitrous oxide concentr...

  17. HARAD, Decay Isotope Concentration from Atmospheric Noble-Gas Release

    International Nuclear Information System (INIS)

    Moore, R.E.

    1986-01-01

    1 - Description of problem or function: HARAD calculates concentrations of radioactive daughters in air following the atmospheric release of a parent radionuclide for a variety of release heights and meteorological conditions. It can be applied most profitably to the assessment of doses to man from the noble gases such as Rn-222, Rn-220, and Xe and Kr isotopes. These gases can produce significant quantities of short-lived particulate daughters in an airborne plume, which are the major contributors to dose. The simultaneous processes of radioactive decay, buildup and environmental loss due to wet and dry deposition on ground surfaces are calculated for a daughter chain in an airborne plume as it is dispersed downwind from a point of release of a parent. 2 - Method of solution: The code evaluates the analytic solution to the set of coupled first order differential equations describing time variation of the concentration of a chain of radionuclides. The analytic solutions assume that the coefficient describing the fractional rate of dry deposition is constant with time. To account for the variation the time coordinate is automatically divided into intervals and a set of average values are used. 3 - Restrictions on the complexity of the problem: - The maximum length of decay chain is 10 nuclides; calculations can be made at a maximum of 24 downwind distances

  18. Study of the superficial ozone concentrations in the atmosphere of Comunidad de Madrid using passive samplers

    Directory of Open Access Journals (Sweden)

    D. Galán Madruga

    2001-06-01

    Full Text Available The ozone is a secondary atmospheric pollutant which is generated for photochemical reactions of volatil organic compounds (VOC’s and nitrogen oxides (NOx. In Spain the ozone is a big problem as a consequence of the solar radiation to reach high levels. Exposure over a period of time to elevated ozone concentrations can cause damage in the public health and alterations in the vegetation.The aim of this study is to carry out the development and validation of a measurement method to let asses the superficial ozone levels in the Comunidad de Madrid, by identifing the zones more significants, where to measure with UV photometric monitors (automatics methods this pollutant and where the health and the vegetation can be affected. To such effect, passive samplers are used, which have glass fiber filters coated with a solution of sodium nitrite, potassium carbonate, glycerol and water. The nitrite ion in the presence of ozone is oxidized to nitrato ion, which it is extrated with ultrapure water and analyzed for ion chromatography, by seen proportional to the concentration existing in the sampling point.The results of validation from field tests indicate a excellent correlation between the passive and the automatic method.The higher superficial ozone concentrations are placed in rural zones, distanced of emission focus of primary pollutants (nitrogen oxides and volatil organic compounds... principally in direction soutwest and northwest of the Comunidad of Madrid.

  19. Valence control of cobalt oxide thin films by annealing atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Wang Shijing [School of Materials Science and Engineering, University of Science and Technology Beijing, No. 30 Xueyuan Road, Beijing 100083 (China); Zhang Boping, E-mail: bpzhang@ustb.edu.cn [School of Materials Science and Engineering, University of Science and Technology Beijing, No. 30 Xueyuan Road, Beijing 100083 (China); Zhao Cuihua; Li Songjie; Zhang Meixia; Yan Liping [School of Materials Science and Engineering, University of Science and Technology Beijing, No. 30 Xueyuan Road, Beijing 100083 (China)

    2011-02-01

    The cobalt oxide (CoO and Co{sub 3}O{sub 4}) thin films were successfully prepared using a spin-coating technique by a chemical solution method with CH{sub 3}OCH{sub 2}CH{sub 2}OH and Co(NO{sub 3}){sub 2}.6H{sub 2}O as starting materials. The grayish cobalt oxide films had uniform crystalline grains with less than 50 nm in diameter. The phase structure is able to tailor by controlling the annealing atmosphere and temperature, in which Co{sub 3}O{sub 4} thin film was obtained by annealing in air at 300-600, and N{sub 2} at 300, and transferred to CoO thin film by raising annealing temperature in N{sub 2}. The fitted X-ray photoelectron spectroscopy (XPS) spectra of the Co2p electrons are distinguishable from different valence states of cobalt oxide especially for their satellite structure. The valence control of cobalt oxide thin films by annealing atmosphere contributes to the tailored optical absorption property.

  20. Atmospheric nitrous oxide produced by solar protons and relativistic electrons

    International Nuclear Information System (INIS)

    Prasad, S.S.; Zipf, E.C.

    1981-01-01

    An alternative means of nitric oxide production in the stratosphere to that of direct formation in the upper atmosphere by solar proton (SP) events and by relativistic electron precipitation (REP) events from the Earth's radiation belt, is described. It is suggested that nitrous oxide is produced in the mesosphere and then migrates downward and is converted in the stratosphere to NO by the reaction N 2 O + O( 1 D) → 2 NO. Such a process could amplify the direct NO production by >10%. Mesospheric nitrous oxide mixing ratios increase to values as high as 6 x 10 -7 due to REP- and SP- related production. Lateral transport will reduce these high values but mesospheric mixing ratios of N 2 O in the high latitudes would approach 10 -7 , considerably greater than those expected on the basis of theories which neglect REP- and SP-related production of this species. (U.K.)

  1. Oxidation behavior of molten magnesium in atmospheres containing SO2

    International Nuclear Information System (INIS)

    Wang Xianfei; Xiong Shoumei

    2011-01-01

    Graphical abstract: Highlights: → We found the film formed on molten magnesium had a two or three layers structure. → The formation mechanism of film was investigated and a growth model was proposed. → We found the formation of MgSO 4 was critical and promoted the growth of the film. - Abstract: The microchemistry and morphology of the oxide layer formed on molten magnesium in atmospheres containing SO 2 were examined. Based on the results and the thermodynamic and kinetic calculations of oxide-growth process, a schematic oxidation mechanism is presented. The results showed that the oxide scales with network structure were generally composed of MgO, MgS, and MgSO 4 with different layers, depending on the SO 2 content, the time and the temperature. The formation of MgSO 4 was important for the formation of the protective oxide scales. The growth of the oxide scales followed the parabolic law at 973 K and was controlled by diffusion.

  2. Atmospheric Concentrations of Persistent Organic Pollutants in the Southern Ocean

    Science.gov (United States)

    Vlahos, P.; Edson, J.; Cifuentes, A.; McGillis, W. R.; Zappa, C.

    2008-12-01

    Long-range transport of persistent organic pollutant (POPs) is a global concern. Remote regions such as the Southern Ocean are greatly under-sampled though critical components in understanding POPs cycling. Over 20 high-volume air samples were collected in the Southern Ocean aboard the RV Brown during the GASEX III experiment between Mar 05 to April 9 2008. The relatively stationary platform (51S,38W) enabled the collection of a unique atmospheric time series at this open ocean station. Air sampling was also conducted across transects from Punto Arenas, Chile and to Montevideo, Uruguay. Samples were collected using glass sleeves packed with poly-urethane foam plugs and C-18 resin in order to collect target organic pollutants (per-fluorinated compounds, currently and historically used pesticides) in this under-sampled region. Here we present POPs concentrations and trends over the sampled period and compare variations with air parcel back trajectories to establish potential origins of their long-range transport.

  3. Nitric Oxide Metabolites and Asymmetric Dimethylarginine Concentrations in Breast Milk

    Directory of Open Access Journals (Sweden)

    Hakan Öztürk

    2017-04-01

    Full Text Available Objective: Nitric oxide plays a preventive role in the development of necrotizing enterocolitis. Oral nitrite and nitrate intake has gained importance with the discovery of the conversion of nitrite to nitric oxide in acidic medium out of the synthesis of nitric oxide from L-arginine. Objective of this study was to examine the breast milk concentrations of nitric oxide and asymmetric dimethylarginine which is a competitive inhibitor of nitric oxide and to compare these concentrations in terms of gestational age and maturity of breast milk. Study Design: Forty-one women were included in the study. Milk samples were collected from 3 groups of mothers as term, late preterm and preterm on the postpartum days 3, 7 and 28. Results: When breast milk concentrations of nitric oxide were compared according to the postnatal day of the milk independently from gestational age; nitric oxide concentration was higher in the colostrum than in the transition milk and mature milk (p=0,035; p=0,001; respectively. For the comparison of asymmetric dimethylarginine concentrations among these groups and days; no statistically significant difference was observed in terms of gestational age and maturity of the milk (p=0.865, p=0.115; respectively. Conclusion: The highest nitric oxide concentration was found in the colostrum, suggesting that colostrum is a valuable food for newborns. Plasma concentrations of asymmetric dimethylarginine were negatively correlated with nitric oxide and did not show a correlation with breast milk, suggesting that asymmetric dimethylargininedoesn’t make nitric oxide inhibition in breast milk.

  4. Comprehensive atmospheric modeling of reactive cyclic siloxanes and their oxidation products

    Science.gov (United States)

    Janechek, Nathan J.; Hansen, Kaj M.; Stanier, Charles O.

    2017-07-01

    Cyclic volatile methyl siloxanes (cVMSs) are important components in personal care products that transport and react in the atmosphere. Octamethylcyclotetrasiloxane (D4), decamethylcyclopentasiloxane (D5), dodecamethylcyclohexasiloxane (D6), and their gas-phase oxidation products have been incorporated into the Community Multiscale Air Quality (CMAQ) model. Gas-phase oxidation products, as the precursor to secondary organic aerosol from this compound class, were included to quantify the maximum potential for aerosol formation from gas-phase reactions with OH. Four 1-month periods were modeled to quantify typical concentrations, seasonal variability, spatial patterns, and vertical profiles. Typical model concentrations showed parent compounds were highly dependent on population density as cities had monthly averaged peak D5 concentrations up to 432 ng m-3. Peak oxidized D5 concentrations were significantly less, up to 9 ng m-3, and were located downwind of major urban areas. Model results were compared to available measurements and previous simulation results. Seasonal variation was analyzed and differences in seasonal influences were observed between urban and rural locations. Parent compound concentrations in urban and peri-urban locations were sensitive to transport factors, while parent compounds in rural areas and oxidized product concentrations were influenced by large-scale seasonal variability in OH.

  5. Red Dawn: Characterizing Iron Oxide Minerals in Atmospheric Dust

    Science.gov (United States)

    Yauk, K.; Ottenfeld, C. F.; Reynolds, R. L.; Goldstein, H.; Cattle, S.; Berquo, T. S.; Moskowitz, B. M.

    2012-12-01

    Atmospheric dust is comprised of many components including small amounts of iron oxide minerals. Although the iron oxides make up a small weight percent of the bulk dust, they are important because of their roles in ocean fertilization, controls on climate, and as a potential health hazard to humans. Here we report on the iron oxide mineralogy in dust from a large dust storm, dubbed Red Dawn, which engulfed eastern Australia along a 3000 km front on 23 September 2009. Red Dawn originated from the lower Lake Eyre Basin of South Australia, western New South Wales (NSW) and southwestern Queensland and was the worst dust storm to have hit the city of Sydney in more than 60 years. Dust samples were collected from various locations across eastern Australia (Lake Cowal, Orange, Hornsby, Sydney) following the Red Dawn event. Our dust collection provides a good opportunity to study the physical and mineralogical properties of iron oxides from Red Dawn using a combination of reflectance spectroscopy, Mössbauer spectroscopy (MB), and magnetic measurements. Magnetization measurements from 20-400 K reveal that magnetite/maghemite, hematite and goethite are present in all samples with magnetite occurring in trace amounts (effects (d< 100 nm). Finally, we compared reflectance with a magnetic parameter (hard isothermal remanent magnetization, HIRM) for ferric oxide abundance to assess the degree to which ferric oxide in these samples might absorb solar radiation. In samples for which both parameters were obtained, HIRM and average reflectance over the visible wavelengths are correlated as a group (r2=0.24). These results indicate that the ferric oxide minerals in Red Dawn dust absorb solar radiation. Much of this ferric oxide occurs likely as grain coatings of nanohematite and nanogoethite, thereby providing high surface area to enhance absorption of solar radiation.

  6. Effect of oxide ion concentration on the electrochemical oxidation of carbon in molten LiCl

    International Nuclear Information System (INIS)

    Yun, J. W.; Choi, I. K.; Park, Y. S.; Kim, W. H.

    2001-01-01

    The continuous measurement of lithium oxide concentration was required in DOR (Direct Oxide Reduction) process, which converts spent nuclear fuel to metal form, for the reactivity monitor and effective control of the process. The concentration of lithium oxide was measured by the electrochemical method, which was based on the phenomenon that carbon atoms of glassy carbon electrode electrochemically react with oxygen ions of lithium oxide in molten LiCl medium. From the results of electrode polarization experiments, the trend of oxidation rate of carbon atoms was classified into two different regions, which were proportional and non-proportional ones, dependent on the amount of lithium oxide. Below about 2.5 wt % Li 2 O, as the carbon atom ionization rate was fast enough for reacting with diffusing lithium oxide to the surface of carbon electrode. In this concentration range, the oxidation rate of carbon atoms was controlled by the diffusion of lithium oxide, and the concentration of lithium oxide could be measured by electrochemical method. But, above 2.5 wt % Li 2 O, the oxidation rate of carbon atoms was controlled by the applied electrochemical potential, because the carbon atom ionization rate was suppressed by the huge amounts of diffusing Li 2 O. Above this concentration, the electrochemical method was not applicable to determine the concentration of lithium oxide

  7. Representative concentration pathways and mitigation scenarios for nitrous oxide

    International Nuclear Information System (INIS)

    Davidson, Eric A

    2012-01-01

    The challenges of mitigating nitrous oxide (N 2 O) emissions are substantially different from those for carbon dioxide (CO 2 ) and methane (CH 4 ), because nitrogen (N) is essential for food production, and over 80% of anthropogenic N 2 O emissions are from the agricultural sector. Here I use a model of emission factors of N 2 O to demonstrate the magnitude of improvements in agriculture and industrial sectors and changes in dietary habits that would be necessary to match the four representative concentration pathways (RCPs) now being considered in the fifth assessment report (AR5) of the Intergovernmental Panel on Climate Change (IPCC). Stabilizing atmospheric N 2 O by 2050, consistent with the most aggressive of the RCP mitigation scenarios, would require about 50% reductions in emission factors in all sectors and about a 50% reduction in mean per capita meat consumption in the developed world. Technologies exist to achieve such improved efficiencies, but overcoming social, economic, and political impediments for their adoption and for changes in dietary habits will present large challenges. (letter)

  8. Auroral nitric oxide concentration and infrared emission

    Science.gov (United States)

    Reidy, W. P.; Degges, T. C.; Hurd, A. G.; Stair, A. T., Jr.; Ulwick, J. C.

    1982-05-01

    Rocket-borne measurements of infrared auroral emission by nitric oxide are analyzed. Four rocket flights provided opportunities to measure 5.3- and 2.7-micron NO emission by means of infrared fixed band radiometers and CVF spectrometers, narrow band photometers, and incident energy spectra on various occasions. Analysis of infrared emission profiles and electron flux data indicates the NO density to be significantly enhanced with respect to midlatitude values. NO emission in the fundamental 5.3-micron band is attributed to resonance excitation by warm earth radiation, collisional excitation primarily by O atoms and chemiluminescence from the reaction of N with O2; with an energy efficiency of 0.015. The overtone band emission at 2.7 microns is accounted for by chemiluminescence produced with an energy efficiency of 0.0054. Total photon yield for the chemiluminescence reaction is estimated to range from 1.2 to 2.4 vibrational quanta per NO molecule.

  9. Investigating Atmospheric Oxidation with Molecular Dynamics Imaging and Spectroscopy

    Science.gov (United States)

    Merrill, W. G.; Case, A. S.; Keutsch, F. N.

    2013-06-01

    Volatile organic compounds (VOCs) in the Earth's atmosphere constitute trace gas species emitted primarily from the biosphere, and are the subject of inquiry for a variety of air quality and climate studies. Reactions intiated (primarily) by the hydroxyl radical (OH) lead to a myriad of oxygenated species (OVOCs), which in turn are prone to further oxidation. Investigations of the role that VOC oxidation plays in tropospheric chemistry have brought to light two troubling scenarios: (1) VOCs are responsible in part for the production of two EPA-regulated pollutants---tropospheric ozone and organic aerosol---and (2) the mechanistic details of VOC oxidation remain convoluted and poorly understood. The latter issue hampers the implementation of near-explicit atmospheric simulations, and large discrepancies in OH reactivity exist between measurements and models at present. Such discrepancies underscore the need for a more thorough description of VOC oxidation. Time-of-flight measurements and ion-imaging techniques are viable options for resolving some of the mechanistic and energetic details of VOC oxidation. Molecular beam studies have the advantage of foregoing unwanted bimolecular reactions, allowing for the characterization of specific processes which must typically compete with the complex manifold of VOC oxidation pathways. The focus of this work is on the unimolecular channels of organic peroxy radical intermediates, which are necessarily generated during VOC oxidation. Such intermediates may isomerize and decompose into distinct chemical channels, enabling the unambiguous detection of each pathway. For instance, a (1 + 1') resonance enhanced multiphoton ionization (REMPI) scheme may be employed to detect carbon monoxide generated from a particular unimolecular process. A number of more subtle mechanistic details may be explored as well. By varying the mean free path of the peroxy radicals in a flow tube, the role of collisional quenching in these unimolecular

  10. Effect of the Lithium Oxide Concentration on a Reduction of Lanthanide Oxides

    International Nuclear Information System (INIS)

    Choi, In-Kyu; Jeong, Myeong-Soo; Do, Jae-Bum; Seo, Chung-Seok

    2007-01-01

    The pyrochemical reduction process of spent oxide fuel is one of the options to handle spent PWR fuels in Korea. After spent oxide fuel is converted to a metallic form, fission products will be removed from the resultant uranium and higher actinide metals by an electrorefining process. The chemical behaviors of lanthanide oxides during the pyrochemical process has been extensively studied. It was also reported that about 30 to 50% of several lanthanide oxides were reduced to corresponding metals by an electrolytic reduction process having 1 wt% of a lithium oxide concentration. Korea Atomic Energy Research Institute (KAERI), however, has been used 3 wt% of lithium oxide to increase the applied current of the electrolytic reduction process. Though it was reported that U 3 O 8 was reduced to uranium metal having a high reduction yield at 3 wt% of the Li 2 O concentration, the effect of the lithium oxide concentration on the reduction of lanthanide oxides has not been clarified

  11. Atmospherically Relevant Radicals Derived from the Oxidation of Dimethyl Sulfide.

    Science.gov (United States)

    Mardyukov, Artur; Schreiner, Peter R

    2018-02-20

    The large number and amounts of volatile organosulfur compounds emitted to the atmosphere and the enormous variety of their reactions in various oxidation states make experimental measurements of even a small fraction of them a daunting task. Dimethyl sulfide (DMS) is a product of biological processes involving marine phytoplankton, and it is estimated to account for approximately 60% of the total natural sulfur gases released to the atmosphere. Ocean-emitted DMS has been suggested to play a role in atmospheric aerosol formation and thereby cloud formation. The reaction of ·OH with DMS is known to proceed by two independent channels: abstraction and addition. The oxidation of DMS is believed to be initiated by the reaction with ·OH and NO 3 · radicals, which eventually leads to the formation of sulfuric acid (H 2 SO 4 ) and methanesulfonic acid (CH 3 SO 3 H). The reaction of DMS with NO 3 · appears to proceed exclusively by hydrogen abstraction. The oxidation of DMS consists of a complex sequence of reactions. Depending on the time of the day or altitude, it may take a variety of pathways. In general, however, the oxidation proceeds via chains of radical reactions. Dimethyl sulfoxide (DMSO) has been reported to be a major product of the addition channel. Dimethyl sulfone (DMSO 2 ), SO 2 , CH 3 SO 3 H, and methanesulfinic acid (CH 3 S(O)OH) have been observed as products of further oxidation of DMSO. Understanding the details of DMS oxidation requires in-depth knowledge of the elementary steps of this seemingly simple transformation, which in turn requires a combination of experimental and theoretical methods. The methylthiyl (CH 3 S·), methylsulfinyl (CH 3 SO·), methylsulfonyl (CH 3 SO 2 ·), and methylsulfonyloxyl (CH 3 SO 3 ·) radicals have been postulated as intermediates in the oxidation of DMS. Therefore, studying the chemistry of sulfur-containing free radicals in the laboratory also is the basis for understanding the mechanism of DMS oxidation in the

  12. The Influence of Atmosphere on the Oxidation of Ground Walnut During Storage at 20 °C

    Directory of Open Access Journals (Sweden)

    Rajko Vidrih

    2012-01-01

    Full Text Available The aim of this study is to determine the impact of atmosphere on the oxidation of ground walnut during storage at 20 °C. Seven varieties of walnut (Juglans regia L. were ground and stored under O2 or N2 atmospheres in hermetically sealed vials for 10 months at room temperature. Antioxidative potential, total phenolic content, fatty acid composition, and oxidative degradation products were determined after 10 months of storage. Cultivar, atmosphere and cultivar×atmosphere interactions significantly influenced the antioxidative potential. Cultivar and atmosphere significantly influenced the content of total polyphenols, with more polyphenols found in walnut stored in the N2 atmosphere. The mass fraction of unsaturated linolenic acid tended to decrease during storage under the O2 atmosphere; statistically significant differences were only found between individual varieties. The O2 atmosphere also resulted in an increase in the synthesis of oxidative degradation products. Among the degradation products, hexanal was the most abundant volatile compound, followed by 1-octen-3-ol, octanal, as well as the mixture of 2-octenal and 1-octen-3-ol. In general, higher concentrations of these degradation products were found in walnut stored under the O2 atmosphere, although these differences were statistically significant only between individual varieties for some compounds.

  13. 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.

  14. A 40-year record of Northern Hemisphere atmospheric carbon monoxide concentration and isotope ratios from the firn at Greenland Summit.

    Science.gov (United States)

    Place, P., Jr.; Petrenko, V. V.; Vimont, I.; Buizert, C.; Lang, P. M.; Edwards, J.; Harth, C. M.; Hmiel, B.; Mak, J. E.; Novelli, P. C.; Brook, E.; Weiss, R. F.; Vaughn, B. H.; White, J. W. C.

    2014-12-01

    Carbon Monoxide (CO) is an important atmospheric trace gas that affects the oxidative capacity of the atmosphere and contributes indirectly to climate forcing by being a major sink of tropospheric OH. A good understanding of the past atmospheric CO budget is therefore important for climate models attempting to characterize recent changes in the atmosphere. Previous work at NEEM, Greenland provided the first reconstructions of Arctic atmospheric history of CO concentration and stable isotope ratios (δC18O and δ13CO) from firn air, dating to the 1950s. In this new study, firn air was sampled from eighteen depth levels through the firn column at Summit, Greenland (in May 2013), yielding a second, independent record of Arctic CO concentration and isotopic ratios. Carbon monoxide stable isotope ratios were analyzed on replicate samples and using a newly developed system with improved precision allowing for a more robust reconstruction. The new CO concentration and stable isotope results overall confirm the earlier findings from NEEM, with a CO concentration peak around the 1970s and higher δC18O and δ13CO values associated with peak CO. Modeling and interpretation of the data are in progress.

  15. Change in the atmospheric concentration of greenhouse gases

    International Nuclear Information System (INIS)

    GARREC, Jean-Pierre

    2000-01-01

    With the constant increase in industrial and agricultural activities since the beginning of the 20. Century, human societies have altered the chemical composition of the atmosphere both in their immediate vicinity and further afar. The most preoccupying problem today is the increase in the so-called greenhouse gases (CO 2 , CH 4 , N 2 O, CFC, O 3 ). Indeed, these pollutant gases generally have long life cycles and consequently have for the first time produced a change in the composition of the atmosphere on a global scale inducing deferred effects such as a likely change in the earth's climate. (author)

  16. NOxTOy: A miniaturised new instrument for reactive nitrogen oxides in the atmosphere

    International Nuclear Information System (INIS)

    Dommen, J.; Prevot, A.S.H.; Neininger, B.; Clark, N.

    2000-01-01

    Emission of nitrogen oxides (NO, NO 2 ) and hydrocarbons into the atmosphere lead, under sunlight, to the formation of ozone and other photo oxidants. To better understand the ozone forming processes, the production and concentration of the nitrogen containing reaction products like nitric acid (HNO 3 ) or peroxyacetylnitrate (PAN) have to be determined. In a joint project with other research institutions and a private enterprise a miniaturised instrument was developed under a KTI contract. It is possible to measure several nitrogen oxides, NO 2 , NO x , NO y , PAN, HNO 3 and O x simultaneously. The dimensions and the power consumption of the instrument are suited for the operation in a motor glider and in a van. First measurements have been successfully performed and are presented. (authors)

  17. Oxidation of elemental mercury in the atmosphere; Constraints imposed by global scale modelling

    Energy Technology Data Exchange (ETDEWEB)

    Bergan, Torbjoern; Rodhe, Henning [Stockholm Univ. (Sweden). Dept. of Meteorology

    2000-05-01

    Based on the global mercury model published by Bergan et al. (1999), we present here further results from simulations where the central theme has been to evaluate the role of ozone and the hydroxyl radical as possible gas phase oxidants for the oxidation of elemental mercury in the atmosphere. The magnitude of natural and man-made mercury emissions are taken from recent literature estimates and the flux from land areas is assumed to vary by season. We consider only two mercury reservoirs, elemental mercury, Hg{sup 0}, and the more soluble divalent form, Hgll. Wet and dry deposition of Hgll is explicitly treated. Applying monthly mean fields of ozone for the oxidation of gas phase Hg{sup 0} and using the reaction rate by Hall (1995) yields a global transformation of Hg{sup 0} to Hgll which is too slow to keep the simulated concentration of Hg{sup 0} near observed values. This shows that there are additional important removal processes for Hg{sup 0} or that the reaction rate proposed by Hall (1995) is too slow. A simulation in which the oxidation rate was artificially increased, so that the global turn-over time of Hg{sup 0} was one year and the simulated average concentration of Hg{sup 0} was realistic, produced latitudinal and seasonal variations in Hg{sup 0} that did not support the hypothesis that gas phase reaction with O{sub 3} is the major oxidation process for Hg{sup 0}. Recent studies indicate that OH may be an important gas phase oxidant for Hg{sup 0}. Using OH as the oxidant and applying the preliminary oxidation rate by Sommar et al. (1999) gave an unrealistically large removal of Hg{sup 0} from the atmosphere. From calculations using a slower reaction rate, corresponding to a turn-over time of Hg{sup 0} of one year, we calculated concentrations of both Hg{sup 0} in surface air and Hgll in precipitation which correspond, both in magnitude and temporal variation, to seasonal observations in Europe and North America. This result supports the suggestion that

  18. The OH-initiated oxidation of atmospheric peroxyacetic acid: Experimental and model studies

    Science.gov (United States)

    Wu, Huihui; Wang, Yin; Li, Huan; Huang, Liubin; Huang, Dao; Shen, Hengqing; Xing, Yanan; Chen, Zhongming

    2017-09-01

    Peroxyacetic acid (PAA, CH3C(O)OOH) plays an important role in atmospheric chemistry, serving as reactive oxidant and affecting radical recycling. However, previous studies revealed an obvious gap between modelled and observed concentrations of atmospheric PAA, which may be partly ascribed to the uncertainty in the kinetics and mechanism of OH-oxidation. In this study, we measured the rate constant of OH radical reaction with PAA (kPAA+OH) and investigated the products in order to develop a more robust atmospheric PAA chemistry. Using the relative rates technique and employing toluene and meta-xylene as reference compounds, the kPAA+OH was determined to be (9.4-11.9) × 10-12 cm3 molecule-1 s-1 at 298 K and 1 atm, which is about (2.5-3.2) times larger than that parameter used in Master Chemical Mechanism v3.3.1 (MCM v3.3.1) (3.70 × 10-12 cm3 molecule-1 s-1). Incorporation of a box model and MCM v3.3.1 with revised PAA chemistry represented a better simulation of atmospheric PAA observed during Wangdu Campaign 2014, a rural site in North China Plain. It is found that OH-oxidation is an important sink of atmospheric PAA in this rural area, accounting for ∼30% of the total loss. Moreover, the major terminal products of PAA-OH reaction were identified as formaldehyde (HCHO) and formic acid (HC(O)OH). The modelled results show that both primary and secondary chemistry play an important role in the large HCHO and HC(O)OH formation under experimental conditions. There should exist the channel of methyl H-abstraction for PAA-OH reaction, which may also provide routes to HCHO and HC(O)OH formation.

  19. Reduction Behaviors of Carbon Composite Iron Oxide Briquette Under Oxidation Atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Ki-Woo; Kim, Kang-Min; Kwon, Jae-Hong; Han, Jeong-Whan [Inha University, Incheon (Korea, Republic of); Son, Sang-Han [POSCO, Pohang (Korea, Republic of)

    2017-01-15

    The carbon composite iron oxide briquette (CCB) is considered a potential solution to the upcoming use of low grade iron resources in the ironmaking process. CCB is able to reduce raw material cost by enabling the use of low grade powdered iron ores and coal. Additionally, the fast reduction of iron oxides by direct contact with coal can be utilized. In this study, the reduction behaviors of CCB were investigated in the temperature range of 200-1200 ℃ under oxidizing atmosphere. Briquettes were prepared by mixing iron ore and coal in a weight ratio of 8:2. Then reduction experiments were carried out in a mixed gas atmosphere of N{sub 2}, O{sub 2}, and CO{sub 2}. Compressive strength tests and quantitative analysis were performed by taking samples at each target temperature. In addition, the reduction degree depending on the reaction time was evaluated by off-gas analysis during the reduction test. It was found that the compressive strength and the metallization degree of the reduced briquettes increased with increases in the reaction temperature and holding time. However, it tended to decrease when the re-oxidation phenomenon was caused by injected oxygen. The degree of reduction reached a maximum value in 26 minutes. Therefore, the re-oxidation phenomenon becomes dominant after 26 minutes.

  20. Simulation of influence of some climatic factors on radiocarbon concentration in the Earth atmosphere

    International Nuclear Information System (INIS)

    Akhmetkereev, S.Kh.; Dergachev, V.A.

    1981-01-01

    The effect of different climatic factors on radiocarbon concentration in the Earth atmosphere is analyzed by modelling the exchange radiocarbon system. It is supposed that the exchange system consists of four reservoirs: long-lived surface vegetation and its remnants, the atmosphere, surface layer of the World ocean. It is shown that the variations of the ocean temperature and the variations in CO 2 amount in the atmosphere connected with it do not affect the atmosphere radiocarbon concentration. Variations in the square of sea ice on the time scale of >=1000 years could bring about variations in the 14 C concentration with the amplitude up to 1%. 14 C concentration in the atmosphere in the icing maximum 18 thousands of years ago was 7% higher than present concentration [ru

  1. Observations of Concentration and δ D of Atmospheric H2 in an Alaskan Boreal Forest

    Science.gov (United States)

    Rahn, T.; Kitchen, N.; Fessenden, J.; Randerson, J. T.; Eiler, J. M.

    2001-12-01

    Molecular hydrogen is the second most abundant reduced gas in the atmosphere with a seasonally dependent mixing ratio averaging ~ 0.5 ppmv; the budget is thought to be controlled by sources from photo-oxidation of hydrocarbons, biomass burning and anthropogenic emissions and sinks dominated by soil uptake and oxidation by OH radicals. We are examining the isotopic signatures of these processes using a new method of H2 recovery and mass spectrometry on sub-liter-sized air samples (i.e., vigorous H2 uptake and were negatively correlated with respiring CO2 (-0.8 to -1.2 ppb H2/ppm CO2). Decreases in H2 concentration are correlated with increases in δ D, indicating that one or more steps in the process of hydrogen consumption (presumably either diffusion into the soil or microbial utilization) is isotopically fractionating. Based on these data, we derive a fractionation factor, α = D/Hresidual/D/Hconsumed = 0.96±0.01. This value is within the range of previous flux-chamber experiments [Gerst and Quay, 2001]. Data from the 24 hour time series yielded a similar nighttime draw down of H2 and elevated CO2 (observable even above canopy) and comparable fractionation factors for D/H. Unexpectedly, samples collected during daylight hours when the canopy was well flushed (evidenced by background CO2 levels) exhibited a modest positive correlation between hydrogen concentration and its deuterium content. We speculate that these enrichments may be the first observational verification of photochemically induced enrichment during oxidation of methane and non-methane hydrocarbons such as that proposed by Gerst and Quay [2001]. Gerst, S. and P. Quay, J. Geophys. Res., 106, 5021-5031, 2001.

  2. Atmospheric pressure plasma enhanced chemical vapor deposition of zinc oxide and aluminum zinc oxide

    International Nuclear Information System (INIS)

    Johnson, Kyle W.; Guruvenket, Srinivasan; Sailer, Robert A.; Ahrenkiel, S. Phillip; Schulz, Douglas L.

    2013-01-01

    Zinc oxide (ZnO) and aluminum-doped zinc oxide (AZO) thin films were deposited via atmospheric pressure plasma enhanced chemical vapor deposition. A second-generation precursor, bis(1,1,1,5,5,5-hexafluoro-2,4-pentanedionato)(N,N′-diethylethylenediamine) zinc, exhibited significant vapor pressure and good stability at one atmosphere where a vaporization temperature of 110 °C gave flux ∼ 7 μmol/min. Auger electron spectroscopy confirmed that addition of H 2 O to the carrier gas stream mitigated F contamination giving nearly 1:1 metal:oxide stoichiometries for both ZnO and AZO with little precursor-derived C contamination. ZnO and AZO thin film resistivities ranged from 14 to 28 Ω·cm for the former and 1.1 to 2.7 Ω·cm for the latter. - Highlights: • A second generation precursor was utilized for atmospheric pressure film growth. • Addition of water vapor to the carrier gas stream led to a marked reduction of ZnF 2 . • Carbonaceous contamination from the precursor was minimal

  3. Urticaceae pollen concentration in the atmosphere of North Western Spain.

    Science.gov (United States)

    Vega-Maray, Ana Maria; Valencia-Barrera, Rosa; Fernandez-Gonzalez, Delia; Fraile, Roberto

    2003-01-01

    Plants of the Urticaceae family can develop into a pest on soils enriched with nitrogen. Urticaceae pollen is a biohazard because it elicits severe pollinosis. Pollen grains were sampled by using a Lanzoni seven-day-recording trap from February 1995-December 2000 in the atmosphere of the city of Ponferrada (Leon, North Western Spain). The Spearman test was used to analyse the statistical correlation between Urticaceae pollen and certain meteorological factors in different main pollination periods. Maximum values are reached in June and July, minimum levels are recorded in January and December. The parameters bearing the greatest positive influence on the occurrence of Urticaceae pollen grains are: temperature (maximum, minimum and mean), humidity (absolute, wet-bulb temperature, dew point and mixing ratio) and south western wind direction; negative parameters are: relative humidity, rainfall and period without wind. The highest correlation coefficients were obtained with temperature and wet-bulb. Absolute humidity and wet-bulb temperature yielded better correlation than relative humidity; hence, these two parameters must be included in this type of study. The use of one main pollination period or another in statistical analysis has an influence on the coefficient value. The behaviour of the pollen grains in the atmosphere during the year also influences the results.

  4. Concentration Impedance in Testing of Solid Oxide Cells Revisited

    DEFF Research Database (Denmark)

    Mogensen, Mogens Bjerg; Ebbesen, Sune Dalgaard; Jensen, Søren Højgaard

    2017-01-01

    The concentration impedance originating from diffusion and reactant conversion impedance of the Ni-YSZ supported fuel electrode in solid oxide cell has been treated many times during the latest couple of decades. In spite of this, the separation of the diffusion impedance from the conversion...

  5. Detection of radon products in atmosphere and its concentration

    International Nuclear Information System (INIS)

    Al-Naemi, H.M.

    1993-01-01

    The climate of the State of Qatar is very warm during the summer and also for considerable parts of the spring and autumn. Energy-tight houses and buildings with air conditioning working day and night for several months are very common. Consequently, the problem of accumulation of indoor radon may exist. No measurements of radon concentration in Qatar have been performed before. The aim of the present work is to implement a suitable technique to measure radon concentration in Qatari houses and buildings. As a first stage, it was found reasonable to start with a technique to evaluate the short-term average indoor radon concentration. The activated charcoal method was chosen to perform this evaluation

  6. REDUCING AMMONIA CONCENTRATIONS IN ATMOSPHERE AFTER ITS UNPLANNED RELEASE

    Directory of Open Access Journals (Sweden)

    L. V. Amelina

    2017-08-01

    Full Text Available Purpose. The aim of this work is development of numerical model, which allows to calculate the efficiency of neutralizer supply for reduction of air pollution in case of unplanned ammonia emission at the territory of ammonia pump station. The numerical model should allow fast calculating, taking into account the meteorological parameters and buildings situated near the source of toxic chemical emission and equipment for neutralizer supply. Methodology. The developed model is based on the equation for potential flow and equation of pollutant dispersion. To simulate the chemical interaction between ammonia and neutralizer the stoichiometry equation is used. Equation of potential flow is used to compute flow pattern among buildings. To solve the equation for potential flow the Samarskii implicit difference scheme is used. The implicit change-triangle difference scheme is used to solve equation of mass transfer. While for the numerical integration the authors use the rectangular difference grid. Method of porosity technique («markers method» is applied to create the form of comprehensive computational region. Emission of ammonia is modeled using Delta function for point source. Findings. Developed numerical model belongs to the class of «diagnostic models». This model takes into account the main physical factors affecting the process of dispersion of ammonia and neutralizer in the atmosphere, as well as the influence of buildings on admixture dispersion. On the basis of the developed numerical models the authors carried out a computational experiment to estimate the efficiency of neutralizer supply for reduction of air pollution in case of unplanned ammonia release at ammonia pump station. Originality. Developed numerical model allows calculating the flow pattern among buildings and estimating the efficiency of neutralizer supply for reduction of air pollution in the case unplanned ammonia release. Practical value. Model allows performing fast

  7. The determinants of atmospheric SO2 concentrations. Reconsidering the environmental Kuznets curve

    International Nuclear Information System (INIS)

    Kaufmann, Robert K.; Davidsdottir, Brynhildur; Garnham, Sophie; Pauly, Peter

    1998-01-01

    This analysis explores the effects of income and the spatial intensity of economic activity on the atmospheric concentration of sulfur dioxide. The results indicate that there is a U-shaped relation between income and atmospheric concentration of SO 2 and an inverted U-shaped relation between the spatial intensity of economic activity and SO 2 concentrations. These results suggest that the spatial intensity of economic activity, rather than income, provides the impetus for policies and technologies that reduce SO 2 emissions. Based on this result, the atmospheric concentration of SO 2 in developing nations may decline faster than indicated by previous analyses. The potential for this decline depends on the rate at which income grows relative to population. The trade-off between the effects of income gains and the spatial intensity of economic activity on the atmospheric concentration of SO 2 is consistent with the notion that environmental problems can be ameliorated by slowing population growth and increasing income levels

  8. Atmospheric mercury concentration and chemical speciation at a rural site in Beijing, China: implications of mercury emission sources

    Directory of Open Access Journals (Sweden)

    L. Zhang

    2013-10-01

    Full Text Available Continuous measurements of atmospheric mercury concentration and speciation play a key role in identifying mercury sources and its behavior in the atmosphere. In this study, speciated atmospheric mercury including gaseous elemental mercury (GEM, reactive gaseous mercury (RGM and particle-bound mercury (PBM were continuously measured at Miyun, a rural site in Beijing, China, from December 2008 to November 2009. The average GEM, RGM and PBM concentrations were found to be 3.22 ± 1.74, 10.1 ± 18.8 and 98.2 ± 112.7 pg m−3, respectively, about 2–20 times higher than the background concentration of the Northern Hemisphere. The results indicated that atmospheric mercury concentrations in northern China were highly affected by anthropogenic emissions. The atmospheric mercury showed obvious seasonal variations, with the highest seasonal average GEM concentration in summer (3.48 ng m−3 and the lowest value in winter (2.66 ng m−3. In autumn and winter a diurnal variation of GEM was observed, with peak levels in the late afternoon till midnight. Most of the high RGM concentration values occurred in the afternoon of all seasons due to the higher oxidation. The PBM concentration was higher in early morning of all seasons because of the the temperature inversion that increases in depth as the night proceeds. The ratio of GEM to CO indicates that residential boilers play an important role in the elevation of GEM in winter. The ratio of RGM to O3 could be an indicator of the contribution of local primary sources. The ratio of PBM to PM2.5 reveals that the air mass from the east and southwest of the site in spring and summer carries more atmospheric mercury. The HYSPLIT back-trajectory analysis indicated that the monitoring site is affected by local, regional and interregional sources simultaneously during heavy pollution episodes. The results from the potential source contribution function (PSCF model indicate that the atmospheric transport

  9. Sensitivity of nitrogen dioxide concentrations to oxides of nitrogen controls in the United Kingdom

    International Nuclear Information System (INIS)

    Dixon, J.

    2001-01-01

    There is a possibility of further controls on emissions to the atmosphere of nitrogen dioxides to meet air quality objectives in the UK. Data in the National Air Quality Archive were used to calculate the likely sensitivity of hourly concentrations of nitrogen dioxide in ambient urban air to changes in the total oxides of nitrogen. Since the role of atmospheric chemical reactions is to make the responses non-linearly dependent on the emissions control, we seek to establish the magnitude and sign of the effects that this non-linearity might cause. We develop a quantitative approach to analysing the non-linearity in the data. Polynomial fits have been developed for the empirical ratio NO 2 :NO x (the 'yield'). They describe nitrogen dioxide concentrations using total oxides of nitrogen. The new functions have the important feature of increased yield in winter episodes. Simpler functions tend to omit this feature of the yields at the highest hourly concentrations. Based on this study, the hourly nitrogen dioxide objective in the UK may require emissions control of no more than about 50% on total oxides of nitrogen at the most polluted sites: other sites require less or even no control. (Author)

  10. Kinetics of a Criegee intermediate that would survive high humidity and may oxidize atmospheric SO2.

    Science.gov (United States)

    Huang, Hao-Li; Chao, Wen; Lin, Jim Jr-Min

    2015-09-01

    Criegee intermediates are thought to play a role in atmospheric chemistry, in particular, the oxidation of SO2, which produces SO3 and subsequently H2SO4, an important constituent of aerosols and acid rain. However, the impact of such oxidation reactions is affected by the reactions of Criegee intermediates with water vapor, because of high water concentrations in the troposphere. In this work, the kinetics of the reactions of dimethyl substituted Criegee intermediate (CH3)2COO with water vapor and with SO2 were directly measured via UV absorption of (CH3)2COO under near-atmospheric conditions. The results indicate that (i) the water reaction with (CH3)2COO is not fast enough (kH2O SO2 at a near-gas-kinetic-limit rate (kSO2 = 1.3 × 10(-10) cm(3) s(-1)). These observations imply a significant fraction of atmospheric (CH3)2COO may survive under humid conditions and react with SO2, very different from the case of the simplest Criegee intermediate CH2OO, in which the reaction with water dimer predominates in the CH2OO decay under typical tropospheric conditions. In addition, a significant pressure dependence was observed for the reaction of (CH3)2COO with SO2, suggesting the use of low pressure rate may underestimate the impact of this reaction. This work demonstrates that the reactivity of a Criegee intermediate toward water vapor strongly depends on its structure, which will influence the main decay pathways and steady-state concentrations for various Criegee intermediates in the atmosphere.

  11. Five pesticides decreased oxidation of atmospheric methane in a forest soil

    DEFF Research Database (Denmark)

    Priemé, Anders; Ekelund, Flemming

    2001-01-01

    We found that five tested pesticides (the insecticide Dimethoat 40 EC, the herbicide Tolkan, and the fungicides Tilt 250 EC, Tilt Top, and Corbel) decreased the oxidation of atmospheric methane in slurries from a Danish forest soil. Dimethoat 40 EC was the most toxic with an EC50 value (i.......e. the concentration which caused a 50% inhibition of the methane oxidation) of 10 mg active ingredient (AI) l-1, followed by Tilt 250 EC (EC50=56 mg AI l-1). EC50 of Tilt Top was 350 AI mg l-1, the value of Tolkan was 410 mg AI l-1, while Corbel had a value of 1600 mg AI l-1. Dimethoat 40 EC and Tolkan inhibited...

  12. Tritium concentration analysis in atmospheric precipitation in Serbia.

    Science.gov (United States)

    Janković, Marija M; Janković, Bojan Ž; Todorović, Dragana J; Ignjatović, Ljubiša M

    2012-01-01

    Tritium activity concentration were monitored in monthly precipitation at five locations in Serbia (Meteorological Station of Belgrade at Zeleno Brdo, Vinča Institute of Nuclear Sciences, Smederevska Palanka, Kraljevo and Niš) over 2005, using electrolytic enrichment and liquid scintillation counting. The obtained concentrations ranged from 3.36 to 127.02 TU. The activity values obtained in samples collected at Zeleno Brdo were lower or close to the minimum detectable activity (MDA), which has a value of 3.36 TU. Significantly higher tritium levels were obtained in samples collected in Vinča Institute of Nuclear Sciences compared with samples from the other investigated locations. Amount of precipitation were also recorded. A good linear correlation (r = 0.75) for Zeleno Brdo and VINS between their tritium activity was obtained. It was found that the value of the symmetrical index n (which indicates the magnitude of tritium content changes with time (months) through its second derivative) is the highest for Vinča Institute of Nuclear Sciences compared to other locations, which is in accordance with the fact that the highest concentrations of tritium were obtained in the samples from the cited place.

  13. An evaluation of the effect of surface chromium concentration on the oxidation of a stainless steel

    International Nuclear Information System (INIS)

    Lobb, R.C.; Evans, H.E.

    1983-01-01

    Short-term oxidation tests have been performed at 850 deg C in a CO 2 -based atmosphere on 20Cr-25Ni-Nb-stabilized steels previously exposed to dynamic vacuum at 1000 deg C. This pre-treatment preferentially removes chromium from the metal surface and is always detrimental to the oxidation properties. It is shown that porous, iron-rich oxides initially form on specimens with surface chromium concentrations 18.5 w/o chromium, a protective surface layer is produced. It is suggested that the transition between these extremes is determined by nucleation conditions and, in the present steels, it is shown how the metal grain size plays a significant role. (author)

  14. The influence of small-scale variations in isoprene concentrations on atmospheric chemistry over a tropical rainforest

    Directory of Open Access Journals (Sweden)

    T. A. M. Pugh

    2011-05-01

    Full Text Available Biogenic volatile organic compounds (BVOCs such as isoprene constitute a large proportion of the global atmospheric oxidant sink. Their reactions in the atmosphere contribute to processes such as ozone production and secondary organic aerosol formation. However, over the tropical rainforest, where 50 % of the global emissions of BVOCs are believed to occur, atmospheric chemistry models have been unable to simulate concurrently the measured daytime concentration of isoprene and that of its principal oxidant, hydroxyl (OH. One reason for this model-measurement discrepancy may be incomplete mixing of isoprene within the convective boundary layer, leading to patchiness or segregation in isoprene and OH mixing ratios and average concentrations that appear to be incompatible with each other. One way of capturing this effect in models of atmospheric chemistry is to use a reduced effective rate constant for their reaction. Recent studies comparing atmospheric chemistry global/box models with field measurements have suggested that this effective rate reduction may be as large as 50 %; which is at the upper limit of that calculated using large eddy simulation models. To date there has only been one field campaign worldwide that has reported co-located measurements of isoprene and OH at the necessary temporal resolution to calculate the segregation of these compounds. However many campaigns have recorded sufficiently high resolution isoprene measurements to capture the small-scale fluctuations in its concentration. Assuming uniform distributions of other OH production and loss processes, we use a box model of atmospheric chemistry, constrained by the spectrum of isoprene concentrations measured, as a virtual instrument, to estimate the variability in OH at a point and hence, to estimate the segregation intensity of isoprene and OH from high-frequency isoprene time series. The method successfully reproduces the only directly observed segregation, using

  15. Atmospherically deposited trace metals from bulk mineral concentrate port operations.

    Science.gov (United States)

    Taylor, Mark Patrick

    2015-05-15

    Although metal exposures in the environment have declined over the last two decades, certain activities and locations still present a risk of harm to human health. This study examines environmental dust metal and metalloid hazards (arsenic, cadmium, lead and nickel) associated with bulk mineral transport, loading and unloading port operations in public locations and children's playgrounds in the inner city of Townsville, northern Queensland. The mean increase in lead on post-play hand wipes (965 μg/m(2)/day) across all sites was more than 10-times the mean pre-play loadings (95 μg/m(2)/day). Maximum loading values after a 10-minute play period were 3012 μg/m(2), more than seven times the goal of 400 μg/m(2) used by the Government of Western Australia (2011). Maximum daily nickel post-play hand loadings (404 μg/m(2)) were more than 26 times above the German Federal Immission Control Act 2002 annual benchmark of 15 μg/m(2)/day. Repeat sampling over the 5-day study period showed that hands and surfaces were re-contaminated daily from the deposition of metal-rich atmospheric dusts. Lead isotopic composition analysis of dust wipes ((208)Pb/(207)Pb and (206)Pb/(207)Pb) showed that surface dust lead was similar to Mount Isa type ores, which are exported through the Port of Townsville. While dust metal contaminant loadings are lower than other mining and smelting towns in Australia, they exceeded national and international benchmarks for environmental quality. The lessons from this study are clear - even where operations are considered acceptable by managing authorities, targeted assessment and monitoring can be used to evaluate whether current management practices are truly best practice. Reassessment can identify opportunities for improvement and maximum environmental and human health protection. Copyright © 2015 Elsevier B.V. All rights reserved.

  16. Decreasing particle number concentrations in a warming atmosphere and implications

    Directory of Open Access Journals (Sweden)

    F. Yu

    2012-03-01

    Full Text Available New particle formation contributes significantly to the number concentration of condensation nuclei (CN as well as cloud CN (CCN, a key factor determining aerosol indirect radiative forcing of the climate system. Using a physics-based nucleation mechanism that is consistent with a range of field observations of aerosol formation, it is shown that projected increases in global temperatures could significantly inhibit new particle, and CCN, formation rates worldwide. An analysis of CN concentrations observed at four NOAA ESRL/GMD baseline stations since the 1970s and two other sites since 1990s reveals long-term decreasing trends that are consistent in sign with, but are larger in magnitude than, the predicted temperature effects. The possible reasons for larger observed long-term CN reductions at remote sites are discussed. The combined effects of rising temperatures on aerosol nucleation rates and other chemical and microphysical processes may imply substantial decreases in future tropospheric particle abundances associated with global warming, delineating a potentially significant feedback mechanism that increases Earth's climate sensitivity to greenhouse gas emissions. Further research is needed to quantify the magnitude of such a feedback process.

  17. Free atmospheric phosphine concentrations and fluxes in different wetland ecosystems, China

    International Nuclear Information System (INIS)

    Han Chao; Geng Jinju; Hong Yuning; Zhang Rui; Gu Xueyuan; Wang Xiaorong; Gao Shixiang; Glindemann, Dietmar

    2011-01-01

    Atmospheric phosphine (PH 3 ) fluxes from typical types of wetlands and PH 3 concentrations in adjacent atmospheric air were measured. The seasonal distribution of PH 3 in marsh and paddy fields were observed. Positive PH 3 fluxes are significantly related to high air temperature (summer season) and increased vegetation. It is concluded that vegetation speeds up the liberation of PH 3 from soils, while water coverage might function as a diffusion barrier from soils or sediments to the atmosphere. The concentrations of atmospheric PH 3 (ng m -3 ) above different wetlands decrease in the order of paddy fields (51.8 ± 3.1) > marsh (46.5 ± 20.5) > lake (37.0 ± 22.7) > coastal wetland (1.71 ± 0.73). Highest atmospheric PH 3 levels in marsh are found in summer. In paddy fields, atmospheric PH 3 concentrations in flourishing stages are higher than those in slowly growing stages. - Research highlights: → P could migrate as PH 3 gas in different wetland ecosystems. → Wetlands act as a source and sink of atmospheric PH 3 . → Positive PH 3 fluxes are significantly related to high temperature and increased vegetation. → Environmental PH 3 concentrations in China are generally higher. - Environmental PH 3 concentrations in China are generally higher compared to other parts of the world.

  18. Implementation of advanced electrochemical oxidation for radiochemical concentrate treatment

    International Nuclear Information System (INIS)

    Velin, Anna; Bengtsson, Bernt; Lundblad, Magnus

    2012-09-01

    Water treatments in Nuclear Power Plants include ion exchange, evaporation and mechanical filtration techniques. These technologies are used to control the chemical release and to treat coolant in light water reactor types from chemicals and most importantly, from radioactive nuclides. Most of the conventional methods are efficient, but at the same time producing aqueous concentrates with high organic load. Before final storage, the level of organic content of those concentrates must be reduced. Advanced electrochemical oxidation with Boron Doped Diamond (BDD) electrodes are being investigated in laboratory- and pilot scale for treatment of dilute and concentrated aqueous waste streams at Vattenfall-Ringhals NPP. BDD anodes and cathodes are having high over potential against water electrolysis, and therefore well suitable for oxidation of organics. Dilute wastewater, such as laundry water, which has an initial COD level of around 500 mg/l, was reduced to a level of < 20 mg/l in the laboratory. Evaporator concentrates, with a TS content of 3% and pH of 7-8, were treated in pilot scale of 800 liters, working in batch operation mode, at temperatures between 25-50 deg. C. Initial COD levels between 2500 and 8000 mg/l in concentrate was reduced to < 100 mg/l at the first tests and later to < 300 mg/l. The advanced electrochemical oxidation is proven to be a promising technique for radioactive concentrate treatment. Long-term operation is still ongoing to evaluate the performance of the electrodes, cell components and overall process efficiency. (authors)

  19. Relationship between carbon-14 concentrations in tree-ring cellulose and atmospheric CO2

    International Nuclear Information System (INIS)

    Yamada, Yoshimune; Yasuike, Kaeko; Komura, Kazuhisa

    2008-01-01

    Concentrations of organically-bound 14 C in the tree-ring cellulose of a Japanese Cedar (Cryptomeria japonica) grown in a rural region of Kanazawa, Ishikawa prefecture, Japan (36.5degN, 136.7degE), were measured for the ring-years from 1989 to 1998 to study relationship between 14 C concentrations in tree-ring cellulose and atmospheric CO 2 in a narrow region. An interesting result in comparing our data of tree-ring cellulose with those of atmospheric CO 2 is that the 14 C concentration in tree-ring cellulose was close to the corresponding average from mid-June to early September of 14 C concentrations in atmospheric CO 2 . Furthermore, the 14 C concentrations in tree-ring cellulose were found to be merely influenced by the drastic decrease of 14 C concentrations in atmospheric CO 2 in winter, which might be caused by air pollution from the Asian continent and additional local fossil fuel contribution. These results suggest that the 14 C concentration in tree-ring cellulose for a given growing year reflects the 14 C concentrations of atmospheric CO 2 during the warm summer months. (author)

  20. Thermal Recycling of Waelz Oxide Using Concentrated Solar Energy

    Science.gov (United States)

    Tzouganatos, N.; Matter, R.; Wieckert, C.; Antrekowitsch, J.; Gamroth, M.; Steinfeld, A.

    2013-12-01

    The dominating Zn recycling process is the so-called Waelz process. Waelz oxide (WOX), containing 55-65% Zn in oxidic form, is mainly derived from electric arc furnace dust produced during recycling of galvanized steel. After its wash treatment to separate off chlorides, WOX is used as feedstock along with ZnS concentrates for the electrolytic production of high-grade zinc. Novel and environmentally cleaner routes for the purification of WOX and the production of Zn are investigated using concentrated solar energy as the source of high-temperature process heat. The solar-driven clinkering of WOX and its carbothermal reduction were experimentally demonstrated using a 10 kWth packed-bed solar reactor. Solar clinkering at above 1265°C reduced the amount of impurities below 0.1 wt.%. Solar carbothermal reduction using biocharcoal as reducing agent in the 1170-1320°C range yielded 90 wt.% Zn.

  1. Concentrations of tritium in atmospheric moisture and precipitation of Mt. Hakkoda

    International Nuclear Information System (INIS)

    Kimura, Hideki; Kon, Takezumi; Sasaki, Mamoru

    2000-01-01

    A large-scale spent nuclear fuel reprocessing plant in Japan is now under construction in Rokkasho Village, Aomori Prefecture. The 3 H will be one of the major radionuclides released from the plant. To grasp the behavior of 3 H in the environment in Aomori Prefecture, we surveyed 3 H concentrations in the atmospheric moisture and the precipitation samples at Mt. Hakkoda. Additional atmospheric moisture samples were collected at Rokkasho Village and Aomori City. The relatively high 3 H concentration in the atmospheric moisture and the precipitation samples at Mt. Hakkoda were observed from spring to summer. The 3 H concentrations in the precipitation were similar to those in the atmospheric moisture. The temporal variation patterns of 3 H concentrations in the atmospheric moisture were similar in relatively wide region that covers from Mt. Hakkoda to Aomori City and Rokkasho Village. The 3 H concentration in atmospheric moisture at the top of Mt. Hakkoda positively correlated with the ozone concentration. It suggested that 3 H originated from the stratosphere, and showed that ozone might be used as an indictor of background 3 H. (author)

  2. A model for oxidizing species concentrations in boiling water reactors

    International Nuclear Information System (INIS)

    Sun, B.; Chexal, B.; Pathania, R.; Chun, J.; Ballinger, R.; Abdollahian, D.

    1993-01-01

    To evaluate and control the intergranular stress corrosion cracking of boiling water reactor (BWR) vessel internal components requires knowledge of the concentration of oxidizing species that affects the electrochemical potentials in various regions of a BWR. In a BWR flow circuit, as water flows through the radiation field, the radiolysis process and chemical reactions lead to the production of species such as oxygen, hydrogen, and hydrogen peroxide. Since chemistry measurements are difficult inside BWRs, analytical tools have been developed by Ruiz and Lin, Ibe and Uchida and Chun and Ballinger for estimating the concentration of species that provide the necessary input for water chemistry control and material protection

  3. Translation Effects in Fluorine Doped Tin Oxide Thin Film Properties by Atmospheric Pressure Chemical Vapour Deposition

    Directory of Open Access Journals (Sweden)

    Mohammad Afzaal

    2016-10-01

    Full Text Available In this work, the impact of translation rates in fluorine doped tin oxide (FTO thin films using atmospheric pressure chemical vapour deposition (APCVD were studied. We demonstrated that by adjusting the translation speeds of the susceptor, the growth rates of the FTO films varied and hence many of the film properties were modified. X-ray powder diffraction showed an increased preferred orientation along the (200 plane at higher translation rates, although with no actual change in the particle sizes. A reduction in dopant level resulted in decreased particle sizes and a much greater degree of (200 preferred orientation. For low dopant concentration levels, atomic force microscope (AFM studies showed a reduction in roughness (and lower optical haze with increased translation rate and decreased growth rates. Electrical measurements concluded that the resistivity, carrier concentration, and mobility of films were dependent on the level of fluorine dopant, the translation rate and hence the growth rates of the deposited films.

  4. Study on influence of native oxide and corrosion products on atmospheric corrosion of pure Al

    International Nuclear Information System (INIS)

    Liu, Yanjie; Wang, Zhenyao; Ke, Wei

    2014-01-01

    Highlights: •Corrosion products layer is only formed in coastal atmosphere. •In coastal atmosphere, rate controlling step is diffusion process. •In rural atmosphere, rate controlling step is charge transfer process. •Pitting area increases greatly in coastal site, but slightly in rural site. -- Abstract: Effects of native oxide and corrosion products on atmospheric corrosion of aluminium in rural and coastal sites were studied by electrochemical impedance spectroscopy (EIS), open-circuit potential (OCP) and scanning electron microscope (SEM) techniques after outdoor exposure. In the rural atmosphere, only the compact, adhesive native oxide layer exists, and the rate controlling step is diffusion process, while in the coastal atmosphere, another loose, inadhesive corrosion products layer exists, and a charge transfer process controls the corrosion process. The pitting area in the coastal atmosphere increases over time more obviously than that in the rural atmosphere

  5. Trends in atmospheric ammonium concentrations in relation to atmospheric sulfate and local agriculture.

    Science.gov (United States)

    Kelly, Victoria R; Lovett, Gary M; Weathers, Kathleen C; Likens, Gene E

    2005-06-01

    Ammonium (NH(4)(+)) concentrations in air and precipitation at the Institute of Ecosystem Studies (IES) in southeastern New York, USA declined over an 11-year period from 1988 to 1999, but increased from 1999 to 2001. These trends in particulate NH(4)(+) correlated well with trends in particulate SO(4)(2-) over the 1988-2001 period. The NH(4)(+) trends were not as well correlated with local cattle and milk production, which declined continuously throughout the period. This suggests that regional transport of SO(4)(2-) may have a greater impact on concentrations of NH(4)(+) and subsequent deposition than local agricultural emissions of NH(3). Ammonium concentrations in precipitation correlated significantly with precipitation SO(4)(2-) concentrations for the 1984-2001 period although NH(4)(+) in precipitation increased after 1999 and SO(4)(2-) in precipitation continued to decline after 1999. The correlation between NH(4)(+) and SO(4)(2-) was stronger for particulates than for precipitation. Particulate NH(4)(+) concentrations were also correlated with particulate SO(4)(2-) concentrations at 31 of 35 eastern U.S. CASTNet sites that had at least 10 years of data. Air concentrations of NH(4)(+) and SO(4)(2-) were more strongly correlated at the sites that were located within an agricultural landscape than in forested sites. At most of the sites there was either no trend or a decrease in NH(4)(+) dry deposition during the 1988-2001 period. The sites that showed an increasing trend in NH(4)(+) dry deposition were generally located in the southeastern U.S. The results of this study suggest that, in the northeastern U.S., air concentrations of NH(4)(+) and subsequent deposition may be more closely linked to SO(4)(2-) and thus SO(2) emissions than with NH(3) emissions. These results also suggest that reductions in S emissions have reduced NH(4)(+) transport to and NH(4)(+)-N deposition in the Northeast.

  6. Tritium concentration reducing method in atmosphere in nuclear reactor containment facility

    International Nuclear Information System (INIS)

    Hirasawa, Yoshiya; Kigoshi, Yasutane; Yonenaga, Haruo.

    1992-01-01

    A portion of water content in an atmosphere is condensed by a condensation/evaporation device disposed in a nuclear reactor containment building and then a portion of the condensed water is evaporated in the atmosphere. A portion of hydrogen nuclides constituting the evaporated water content is subjected to isotopic exchange with tritium nuclides in the atmosphere. A portion of water content in the atmosphere applied with the isotopic exchange is condensed in the condensation/evaporation device. That is, the hydrogen nuclides in steams are applied with isotopic exchange with tritium nuclides, and steams incorporating tritium nuclides are condensed again in the condensation/evaporation device, to transfer the tritium nuclides in the atmosphere to condensed water. The condensed water is recovered without releasing the tritium nuclides to the outside of the reactor containment building, thereby enabling to reduce the tritium concentration in the atmosphere. (N.H.)

  7. Oxidation-sulfidation behavior of Ni aluminide in oxygen-sulfur mixed-gas atmospheres

    International Nuclear Information System (INIS)

    Natesan, K.

    1988-01-01

    Oxidation-sulfidation studies were conducted with sheet samples of nickel aluminide, containing 23.5 at. % Al, 0.5 at. % Hf, and 0.2 at. % B, in an annealed condition and after preoxidation treatments. Continuous weight-change measurements were made by a thermogravimetric technique in exposure atmospheres of air, a low-pO/sub 2/ gas mixture, and low-pO/sub 2/ gas mixtures with several levels of sulfur. The air-exposed specimens developed predominantly nickel oxide; the specimen exposed to a low-pO/sub 2/ environment developed an aluminum oxide scale. As the sulfur content of the gas mixture increased, the alumina scale exhibited spallation and the alloy tended to form nickel sulfide as the reaction phase. The results indicated that the sulfidation reaction of nickel aluminide specimens (both bare and preoxidized) was determined by the rate of transport of nickel from the substrate through the scale to the gas/alumina scale interface, the mechanical integrity of the oxide scale, and the H/sub 2/S concentration in the exposure environment

  8. Oxidation in fish oil-enriched mayonnaise 4 : Effect of tocopherol concentration on oxidative deterioration

    DEFF Research Database (Denmark)

    Jacobsen, Charlotte; Hartvigsen, Karsten; Lund, Pia

    2001-01-01

    The effect of the water-dispersible tocopherol preparation, Grindox 1032, and the oil-soluble tocopherol preparation, Toco 70, on oxidative stability in fish oil-enriched mayonnaise was examined. The two commercial antioxidant preparations were supplemented in different levels corresponding to 20......-280 ppm tocopherol in addition to the 600 ppm present in the oils used for the mayonnaise. The oxidative stability was assessed by sensory analysis, the tendency of formation of free radicals, and concentrations of lipid hydroperoxides and volatile oxidation products. The effect of tocopherol on oxidation...... depended on the nature and the concentration of the tocopherol preparation employed, and it also depended on the parameters evaluated. Addition of high levels of Grindox 1032 (similar to 140-280 ppm tocopherol) thus decreased the intensity of rancid off-flavor, but increased the formation of fishy off...

  9. Lipid oxidation and color changes of goose meat stored under vacuum and modified atmosphere conditions.

    Science.gov (United States)

    Orkusz, A; Haraf, G; Okruszek, A; Werenska-Sudnik, M

    2017-03-01

    The objective of the work was to investigate the color and lipid oxidation changes of goose breast meat packaged in vacuum and modified atmosphere (MA) conditions consisting of 80% O2, 20% CO2, and stored in refrigerated conditions at 4°C. Color stability was monitored by determining total heme pigments concentration; relative concentration of myoglobin, oxymyoglobin, and metmyoglobin; parameters of color L*, a*, b*, and sensory evaluation of the surface color. Lipid stability was measured by determining thiobarbituric acid reactive substances (TBARS). The samples were examined in 24 h after slaughter (unpacked muscles) and on d 4, 7, 9, 11 of storage (muscles packed in vacuum and in MA). Through the time of storage, samples packed in MA had higher TBARS values in comparison to the meat packed in vacuum. For samples packed in two types of atmospheres, the total pigments concentration decreased gradually within 11 d of storage. It was observed that relative metmyoglobin concentration increased whereas relative oxymyoglobin concentration decreased in total heme pigments in the MA stored muscle. The relative concentration of all three myoglobin forms sample packed in vacuum remained unchanged. The color parameters (L*, a*, b*) did not change for 11 d of storage for the vacuum packed meat. The value of the color parameter a* decreased and the value of the color parameters L* and b* increased in the samples packaged in MA. The data prove that if you store goose meat in MA (consisting of 80% O2, 20% CO2) or vacuum, the unchanged surface color is preserved for 9 and 11 day, respectively.Vacuum appears to be a better method as regards the maintaining of lipid stability in goose meat. © 2016 Poultry Science Association Inc.

  10. Exhaled nitric oxide concentration in patients after heart transplantation.

    Science.gov (United States)

    Nadziakiewicz, P; Knapik, P; Zakliczyński, M; Zembala, M; Urbańska, E; Pacholewicz, J

    2007-11-01

    Nitric oxide (NO) is present in exhaled air in humans and its level may decrease in heart diseases. In the present study we prospectively investigated how heart transplantation treated with oral immunosuppresive drugs based on ciclosporine A influences the exhaled NO concentration (exNO). The study was performed in 17 patients after heart transplantation in various time after procedure and 15 nonsmoking healthy volunteers as a control group. Patients after heart transplantation were free of clinical signs of rejection. End-tidal concentration of exNO was measured by the use of a chemiluminescence method. We found no statistically significant differences in the exNO level between patients after heart transplantation and healthy controls (6.81+/-2.70 part per billion (ppb) in the transplant group vs. 6.01+/-3.43 ppb in the control group). We conclude that heart transplantation and immunosuppresive therapy do not influence the exhaled NO concentration.

  11. Study of the effects of atmospheric parameters on ground radon concentration by track technique

    International Nuclear Information System (INIS)

    Tidjani, Adams

    1988-01-01

    Radon emanation was continuously monitored for 24 months, accompanied by measurements of atmospheric parameters. Integrated measurments of radon concentrations have been performed with LR-115 cellulose nitrate track detectors. The monitoring was conducted at 16 sites distributed around the Dakar University area. Observed changes in radon concentration are interpreted as being caused by changes in meteorological conditions and ocean tides. (author)

  12. Determining How Atmospheric Carbon Dioxide Concentrations Have Changed during the History of the Earth

    Science.gov (United States)

    Badger, Marcus P. S.; Pancost, Richard D.; Harrison, Timothy G.

    2011-01-01

    The reconstruction of ancient atmospheric carbon dioxide concentrations is essential to understanding the history of the Earth and life. It is also an important guide to identifying the sensitivity of the Earth system to this greenhouse gas and, therefore, constraining its future impact on climate. However, determining the concentration of…

  13. Atmospheric Oxidation of Squalene: Molecular Study Using COBRA Modeling and High-Resolution Mass Spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Fooshee, David R.; Aiona, Paige K.; Laskin, Alexander; Laskin, Julia; Nizkorodov, Sergey; Baldi, Pierre

    2015-10-22

    Squalene is a major component of skin and plant surface lipids, and is known to be present at high concentrations in indoor dust. Its high reactivity toward ozone makes it an important ozone sink and a natural protectant against atmospheric oxidizing agents. While the volatile products of squalene ozonolysis are known, the condensed-phase products have not been characterized. We present an analysis of condensed-phase products resulting from an extensive oxidation of squalene by ozone probed by electrospray ionization (ESI) high-resolution mass spectrometry (HR-MS). A complex distribution of nearly 1,300 peaks assignable to molecular formulas is observed in direct infusion positive ion mode ESI mass spectra. The distribution of peaks in the mass spectra suggests that there are extensive cross-coupling reactions between hydroxy-carbonyl products of squalene ozonolysis. To get additional insights into the mechanism, we apply a Computational Brewing Application (COBRA) to simulate the oxidation of squalene in the presence of ozone, and compare predicted results with those observed by the HR-MS experiments. The system predicts over one billion molecular structures between 0-1450 Da, which correspond to about 27,000 distinct elemental formulas. Over 83% of the squalene oxidation products inferred from the mass spectrometry data are matched by the simulation. Simulation indicates a prevalence of peroxy groups, with hydroxyl and ether groups being the second-most important O-containing functional groups formed during squalene oxidation. These highly oxidized products of squalene ozonolysis may accumulate on indoor dust and surfaces, and contribute to their redox capacity.

  14. Impacts of Four SO2 Oxidation Pathways on Wintertime Sulfate Concentrations

    Science.gov (United States)

    Sarwar, G.; Fahey, K.; Zhang, Y.; Kang, D.; Mathur, R.; Xing, J.; Wei, C.; Cheng, Y.

    2017-12-01

    Air quality models tend to under-estimate winter-time sulfate concentrations compared to observed data. Such under-estimations are particularly acute in China where very high concentrations of sulfate have been measured. Sulfate is produced by oxidation of sulfur dioxide (SO2) in gas-phase by hydroxyl radical and in aqueous-phase by hydrogen peroxide, ozone, etc. and most air quality models employ such typical reactions. Several additional SO2 oxidation pathways have recently been proposed. Heterogeneous reaction on dust has been suggested to be an important sink for SO2. Oxidation of SO2 on fine particles in presence of nitrogen dioxide (NO2) and ammonia (NH3) at high relative humidity has been implicated for sulfate formation in Chinese haze and London fog. Reactive nitrogen chemistry in aerosol water has also been suggested to produce winter-time sulfate in China. Specifically, high aerosol water can trap SO2 which can be subsequently oxidized by NO2 to form sulfate. Aqueous-phase (in-cloud) oxidation of SO2 by NO2 can also produce sulfate. Here, we use the hemispheric Community Multiscale Air Quality (CMAQ) modeling system to examine the potential impacts of these SO2 oxidation pathways on sulfate formation. We use anthropogenic emissions from the Emissions Database for Global Atmospheric Research and biogenic emissions from Global Emissions InitiAtive. We performed simulations without and with these SO2 oxidation pathways for October-December of 2014 using meteorological fields obtained from the Weather Research and Forecasting model. The standard CMAQ model contains one gas-phase chemical reaction and five aqueous-phase chemical reactions for SO2 oxidation. We implement four additional SO2 oxidation pathways into the CMAQ model. Our preliminary results suggest that the dust chemistry enhances mean sulfate over parts of China and Middle-East, the in-cloud SO2 oxidation by NO2 enhances sulfate over parts of western Europe, oxidation of SO2 by NO2 and NH3 on

  15. Atmospheric concentration of 210Pb at Beijing and Chengdu, the People's Republic of China

    International Nuclear Information System (INIS)

    Sato, Shin; Sato, Jun; Doi, Taeko

    2000-01-01

    Atmospheric concentrations of 210 Pb were observed in the eastern area of the People's Republic of China with aerosol samples. Observations were carried out intermittently during the period from April, 1989 to December, 1992 at Beijing and Chengdu. The atmospheric concentrations of 210 Pb ranged from 0.9 to 4.6 mBq/m 3 at Beijing and from 1.4 to 7.8 mBq/m 3 at Chengdu, respectively, which were in the similar level to those observed previously in the inland area of the Chinese Continent. Seasonal variations of the 210 Pb concentration show the 'one-peak' variation pattern: the maximum levels were recorded in winter season. Small additional rises in the atmospheric 210 Pb concentrations observed in the period from spring to autumn seasons may be due to complicated meteorology with high pressure systems at Beijing and due to the topographical situation at Chengdu. (author)

  16. Detection of nitric acid and nitric oxides in the terrestrial atmosphere in the middle-infrared spectral region

    Directory of Open Access Journals (Sweden)

    M. I. Blecka

    1996-11-01

    Full Text Available A proposal for combined space and ground-based observations of the vertical distributions and the column densities of nitric acid and nitric oxide concentrations in the earth's atmosphere is discussed. We focus on the aspects that are particular to the idea of correlative measurements: geometrical considerations, simulations of the solar absorption spectra in the middle-infrared region corresponding to the different observational geometries, and the associated retrieval methods. These studies are done specifically for the Belgian-French experiment MIRAS (MIR Infrared Atmospheric Spectrometer onboard the Russian Space Station MIR and correlative ground-based FTIR measurements in the Tatra mountains.

  17. The optimal atmospheric CO2 concentration for the growth of winter wheat (Triticum aestivum).

    Science.gov (United States)

    Xu, Ming

    2015-07-20

    This study examined the optimal atmospheric CO2 concentration of the CO2 fertilization effect on the growth of winter wheat with growth chambers where the CO2 concentration was controlled at 400, 600, 800, 1000, and 1200 ppm respectively. I found that initial increase in atmospheric CO2 concentration dramatically enhanced winter wheat growth through the CO2 fertilization effect. However, this CO2 fertilization effect was substantially compromised with further increase in CO2 concentration, demonstrating an optimal CO2 concentration of 889.6, 909.4, and 894.2 ppm for aboveground, belowground, and total biomass, respectively, and 967.8 ppm for leaf photosynthesis. Also, high CO2 concentrations exceeding the optima not only reduced leaf stomatal density, length and conductance, but also changed the spatial distribution pattern of stomata on leaves. In addition, high CO2 concentration also decreased the maximum carboxylation rate (Vc(max)) and the maximum electron transport rate (J(max)) of leaf photosynthesis. However, the high CO2 concentration had little effect on leaf length and plant height. The optimal CO2 fertilization effect found in this study can be used as an indicator in selecting and breeding new wheat strains in adapting to future high atmospheric CO2 concentrations and climate change. Copyright © 2015. Published by Elsevier GmbH.

  18. Effect of oxygen level on the oxidative stability of two different retail pork products stored using modified atmosphere packaging (MAP)

    DEFF Research Database (Denmark)

    Spanos, Dimitrios; Ann Tørngren, Mari; Christensen, Mette

    2016-01-01

    The characteristics and the oxidative stability of pork steaks and of pork mince were investigated during 2, 5 and 7 days of refrigerated storage using oxygen (O2) levels of 0%, 20%, 50% and 80% in modified atmosphere packaging (MAP). Steaks stored during 7 days were not affected by an increase i......%) O2 MAP. The results show that fresh pork products are affected differently by the MAP O2 concentration and strongly indicate that optimisation of MAP based on the retail product type would be of considerable benefit to their oxidative stability....

  19. Mathematical modeling of atmospheric fine particle-associated primary organic compound concentrations

    Science.gov (United States)

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

    1996-08-01

    An atmospheric transport model has been used to explore the relationship between source emissions and ambient air quality for individual particle phase organic compounds present in primary aerosol source emissions. An inventory of fine particulate organic compound emissions was assembled for the Los Angeles area in the year 1982. Sources characterized included noncatalyst- and catalyst-equipped autos, diesel trucks, paved road dust, tire wear, brake lining dust, meat cooking operations, industrial oil-fired boilers, roofing tar pots, natural gas combustion in residential homes, cigarette smoke, fireplaces burning oak and pine wood, and plant leaf abrasion products. These primary fine particle source emissions were supplied to a computer-based model that simulates atmospheric transport, dispersion, and dry deposition based on the time series of hourly wind observations and mixing depths. Monthly average fine particle organic compound concentrations that would prevail if the primary organic aerosol were transported without chemical reaction were computed for more than 100 organic compounds within an 80 km × 80 km modeling area centered over Los Angeles. The monthly average compound concentrations predicted by the transport model were compared to atmospheric measurements made at monitoring sites within the study area during 1982. The predicted seasonal variation and absolute values of the concentrations of the more stable compounds are found to be in reasonable agreement with the ambient observations. While model predictions for the higher molecular weight polycyclic aromatic hydrocarbons (PAH) are in agreement with ambient observations, lower molecular weight PAH show much higher predicted than measured atmospheric concentrations in the particle phase, indicating atmospheric decay by chemical reactions or evaporation from the particle phase. The atmospheric concentrations of dicarboxylic acids and aromatic polycarboxylic acids greatly exceed the contributions that

  20. Study on the surface oxidation of uranium in different gaseous atmospheres

    International Nuclear Information System (INIS)

    Wang Xiaoling; Fu Yibei; Xie Renshou

    1996-03-01

    The studying for the surface oxidation of uranium and oxide by X-ray photoelectron spectroscopy (XPS), Auger electron spectroscopy (AES), secondary ion mass spectroscopy (SIMS), and the surface oxidation of uranium in different gaseous atmospheres such as O 2 , H 2 , CO, CO 2 , H 2 O(v) and air were reviewed. The surface oxidation of uranium is greatly influenced by a number of parameters including atmospheric temperature, pressure, diffusion of adsorbed gas atoms through the oxide layer, surface and interface chemical component, and defect structure and electron nature of the oxide layer. The initial oxidation mechanism and kinetics have been discussed. Suggestions for future work have also been presented. (32 refs., 7 figs., 5 tabs.)

  1. 222Rn and 14CO2 concentrations in the surface layer of the atmosphere

    International Nuclear Information System (INIS)

    Holy, K.; Chudy, M.; Sivo, A.; Richtarikova, M.; Boehm, R.; Polaskova, A.; Vojtyla, P.; Bosa, I.; Hola, O.

    2002-01-01

    Long-term monitoring of the Δ 14 C in the atmospheric near-ground CO 2 has been realized in Bratislava and Zlkovce, situated near the nuclear power plant Jaslovske Bohunice. Until 1993, the monthly mean Δ 14 C values showed a high variability. The annual means of Δ 14 C were about 30 per mille higher at Zlkovce than in highly industrialised Bratislava. An important change in the behaviour of the 14 C data has occurred since 1993. The records from both stations show the similar course, mainly due to the fact that there do not occur deep winter minima in Bratislava. This behaviour corresponds to the lower values of the total fossil fuel CO 2 emissions in the years after 1993 when compared to the previous years. At present, both sets of data show that the 14 C concentration is about 10% above the natural level. Since 1987 also the 222 Rn concentration in the surface layer of the atmosphere has been measured in Bratislava. These measurements provided an extensive set of the 222 Rn data characteristic for the inland environment with high level of atmospheric pollution. The seasonal and daily variations of the 222 Rn concentration were observed. The investigation of the relation between the monthly mean diurnal courses of the 222 Rn concentration and the atmospheric stability proved a high correlation between them. The 222 Rn data were used to interpret the anomalous Δ 14 C values in the surface layer of the atmosphere. (author)

  2. Calcination of the cerium concentrate to be cerium oxide

    International Nuclear Information System (INIS)

    Suyanti; MV Purwani

    2016-01-01

    Calcination of the cerium concentrate to be cerium oxide has done. The cerium concentrate were obtained from the Ce making process wear KBrO_3 and without using KBrO_3. The calcination were done with a variation of time 1, 2, 3 and 4 hours with the temperature variations of 700, 800 and 900°C. The easiest calcination of Ce concentrates to be CeO_2 containing majority of Ce(OH)_4 and contains least impurities as Th(OH)_4, (NH_4)_2Y(NO_3), H_4N_5O_1_2La, H_1_2N_3NdO_1_5 and N_3O_9Sm. On the calcination of Ce concentrates process results without using KBrO_3 1, the calcination temperature 900°C was obtained CeO_2 content of 73.53% for calcination time of 4 hours, has little difference when compared with the predictions and calculation result of complete calcination was equal 73.84%. (author)

  3. Concentrations of organochlorine pesticides, polybrominated diphenyl ethers and perfluorinated compounds in the atmosphere of North Greenland

    DEFF Research Database (Denmark)

    Bossi, Rossana; Vorkamp, Katrin; Skov, Henrik

    2016-01-01

    Atmospheric concentrations of organochlorine pesticides (OCPs), polybrominated diphenyl ethers (PBDEs) and neutral per- and polyfluoroalkyl substances (PFAS) have been measured at Villum Research Station, Station Nord (North Greenland) in the period 2008–2013. Atmospheric concentrations of OCPs...... for neutral PFAS we present for the first time a multiyear series of measurements for North Greenland. The average sum of the seven measured neutral PFAS (∑7PFAS) ranged from 1.82 to 32.1 pg m−3. The most abundant compound was 8:2 FTOH (44% of ∑7PFAS), followed by 6:2 FTOH and 10:2 FTOH. Perfluoroalkyl...

  4. Prediction on long-term mean and mean square pollutant concentrations in an urban atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, S; Lamb, R G; Seinfeld, J H

    1976-01-01

    The general problem of predicting long-term average (say yearly) pollutant concentrations in an urban atmosphere is formulated. The pollutant concentration can be viewed as a random process, the complete description of which requires knowledge of its probability density function, which is unknown. The mean concentration is the first moment of the concentration distribution, and at present there exist a number of models for predicting the long-term mean concentration of an inert pollutant. The second moment, or mean square concentration, indicates additional features of the distribution, such as the level of fluctuations about the mean. In the paper a model proposed by Lamb for the long-term mean concentration is reviewed, and a new model for prediction of the long-term mean square concentration of an inert air pollutant is derived. The properties and uses of the model are discussed, and the equations defining the model are presented in a form for direct application to an urban area.

  5. Sintering of uranium dioxide pellets (UO2) in an oxidizing atmosphere (C O2)

    International Nuclear Information System (INIS)

    Santos, G.R.T.

    1992-01-01

    This work consists in the study of the sintering process of U O 2 pellets in an oxidizing atmosphere. Sintering tests were performed in an CO 2 atmosphere and the influence of temperature and time on the pellets density and microstructure were verified. The results obtained were compared to those from the conventional sintering process and its efficiency was confirmed. (author)

  6. Effect of wind speed and relative humidity on atmospheric dust concentrations in semi-arid climates.

    Science.gov (United States)

    Csavina, Janae; Field, Jason; Félix, Omar; Corral-Avitia, Alba Y; Sáez, A Eduardo; Betterton, Eric A

    2014-07-15

    Atmospheric particulate have deleterious impacts on human health. Predicting dust and aerosol emission and transport would be helpful to reduce harmful impacts but, despite numerous studies, prediction of dust events and contaminant transport in dust remains challenging. In this work, we show that relative humidity and wind speed are both determinants in atmospheric dust concentration. Observations of atmospheric dust concentrations in Green Valley, AZ, USA, and Juárez, Chihuahua, México, show that PM10 concentrations are not directly correlated with wind speed or relative humidity separately. However, selecting the data for high wind speeds (>4m/s at 10 m elevation), a definite trend is observed between dust concentration and relative humidity: dust concentration increases with relative humidity, reaching a maximum around 25% and it subsequently decreases with relative humidity. Models for dust storm forecasting may be improved by utilizing atmospheric humidity and wind speed as main drivers for dust generation and transport. Copyright © 2014 Elsevier B.V. All rights reserved.

  7. Long-term decline of global atmospheric ethane concentrations and implications for methane.

    Science.gov (United States)

    Simpson, Isobel J; Sulbaek Andersen, Mads P; Meinardi, Simone; Bruhwiler, Lori; Blake, Nicola J; Helmig, Detlev; Rowland, F Sherwood; Blake, Donald R

    2012-08-23

    After methane, ethane is the most abundant hydrocarbon in the remote atmosphere. It is a precursor to tropospheric ozone and it influences the atmosphere's oxidative capacity through its reaction with the hydroxyl radical, ethane's primary atmospheric sink. Here we present the longest continuous record of global atmospheric ethane levels. We show that global ethane emission rates decreased from 14.3 to 11.3 teragrams per year, or by 21 per cent, from 1984 to 2010. We attribute this to decreasing fugitive emissions from ethane's fossil fuel source--most probably decreased venting and flaring of natural gas in oil fields--rather than a decline in its other major sources, biofuel use and biomass burning. Ethane's major emission sources are shared with methane, and recent studies have disagreed on whether reduced fossil fuel or microbial emissions have caused methane's atmospheric growth rate to slow. Our findings suggest that reduced fugitive fossil fuel emissions account for at least 10-21 teragrams per year (30-70 per cent) of the decrease in methane's global emissions, significantly contributing to methane's slowing atmospheric growth rate since the mid-1980s.

  8. Quantification of atmospheric oxygen levels during the Paleoproterozoic using paleosol compositions and iron oxidation kinetics

    Science.gov (United States)

    Murakami, Takashi; Sreenivas, Bulusu; Sharma, Subrata Das; Sugimori, Hirokazu

    2011-07-01

    The increase in atmospheric oxygen during the Precambrian is a key to understand the co-evolution of life and environment and has remained as a debatable topic. Among various proxies for the estimation of atmospheric oxygen levels, paleosols, ancient weathering profiles, can provide a quantitative pattern of atmospheric oxygen increase during the Precambrian period of Earth history. We have re-evaluated the chemical compositions of paleosols, and presented a new method of applying Fe 2+ oxidation kinetics to the Fe 2+ and Fe 3+ concentrations in paleosols to decipher the quantitative partial pressure of atmospheric oxygen ( P) between 2.5 and 2.0 Ga. We first estimated the compaction factor ( CF, the fraction of original thickness) using the immobile elements such as Ti, Al and Zr on equal volume basis, which was then used to calculate retention fractions ( M R), a mass ratio of paleosol to parent rock, of redox-sensitive elements. The CF and Fe R values were evaluated for factors such as homogeneity of immobile elements, erosion, and formation time of weathering. Fe R increased gradually within the time window of ˜2.5-2.1 Ga and remained close to 1.0 since ˜2.1 Ga onwards. Mn R also increased gradually similar to Fe R but at a slower rate and near complete retention was observed ˜1.85 Ga, suggesting an almost continuous increase in the oxidation of Fe 2+ and Mn 2+ in paleosols ranging in age between ˜2.5 and 1.9 Ga. We have modeled P variations during the Paleoproterozoic by applying Fe 2+ oxidation kinetics to the Fe 2+ and Fe 3+ concentrations in paleosols, which enabled us to derive an Fe 2+ oxidation term referred to as ψ. Possible changes in temperature and P during this time window and their effects on resulting models of P evolution have been also considered. We assumed four cases for the calculations of P variations between 2.5 and 2.0 Ga: no change in either temperature or P, long-term change in only P, long-term changes in both temperature and P

  9. Volume concentration of 41 elements in ground level of atmosphere in Bratislava

    International Nuclear Information System (INIS)

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

    2006-01-01

    The concentrations of 41 chemical elements (heavy metals, rare earths, and actinides) were determined in atmospheric aerosol using nuclear and related analytical techniques. The sampling location was in Bratislava (Slovak Republic). The main goal of this study is the quantification of the atmospheric pollution and its trend. The elemental content in filters was measured using instrumental neutron activation analysis at IBR-2 reactor in JINR Dubna and by atomic absorption spectrometry in Bratislava. The obtained results confirmed the decreasing trend of pollution by most of the heavy metals in Bratislava atmosphere, and they are compared with the contents of pollutants in atmosphere of other cities. We determined also the composition of clear filter materials. (authors)

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

    Science.gov (United States)

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

    2012-01-01

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

  11. Challenge for lowering concentration polarization in solid oxide fuel cells

    Science.gov (United States)

    Shimada, Hiroyuki; Suzuki, Toshio; Yamaguchi, Toshiaki; Sumi, Hirofumi; Hamamoto, Koichi; Fujishiro, Yoshinobu

    2016-01-01

    In the scope of electrochemical phenomena, concentration polarization at electrodes is theoretically inevitable, and lowering the concentration overpotential to improve the performance of electrochemical cells has been a continuing challenge. Electrodes with highly controlled microstructure, i.e., high porosity and uniform large pores are therefore essential to achieve high performance electrochemical cells. In this study, state-of-the-art technology for controlling the microstructure of electrodes has been developed for realizing high performance support electrodes of solid oxide fuel cells (SOFCs). The key is controlling the porosity and pore size distribution to improve gas diffusion, while maintaining the integrity of the electrolyte and the structural strength of actual sized electrode supports needed for the target application. Planar anode-supported SOFCs developed in this study realize 5 μm thick dense electrolyte (yttria-stabilized zirconia: YSZ) and the anode substrate (Ni-YSZ) of 53.6 vol.% porosity with a large median pore diameter of 0.911 μm. Electrochemical measurements reveal that the performance of the anode-supported SOFCs improves with increasing anode porosity. This Ni-YSZ anode minimizes the concentration polarization, resulting in a maximum power density of 3.09 W cm-2 at 800 °C using humidified hydrogen fuel without any electrode functional layers.

  12. An approach for verifying biogenic greenhouse gas emissions inventories with atmospheric CO2 concentration data

    Science.gov (United States)

    Stephen M Ogle; Kenneth Davis; Thomas Lauvaux; Andrew Schuh; Dan Cooley; Tristram O West; Linda S Heath; Natasha L Miles; Scott Richardson; F Jay Breidt; James E Smith; Jessica L McCarty; Kevin R Gurney; Pieter Tans; A Scott. Denning

    2015-01-01

    Verifying national greenhouse gas (GHG) emissions inventories is a critical step to ensure that reported emissions data to the United Nations Framework Convention on Climate Change (UNFCCC) are accurate and representative of a country's contribution to GHG concentrations in the atmosphere. Furthermore, verifying biogenic fluxes provides a check on estimated...

  13. Estimating Terrestrial Wood Biomass from Observed Concentrations of Atmospheric Carbon Dioxide

    NARCIS (Netherlands)

    Schaefer, K. M.; Peters, W.; Carvalhais, N.; van der Werf, G.; Miller, J.

    2008-01-01

    We estimate terrestrial disequilibrium state and wood biomass from observed concentrations of atmospheric CO2 using the CarbonTracker system coupled to the SiBCASA biophysical model. Starting with a priori estimates of carbon flux from the land, ocean, and fossil fuels, CarbonTracker estimates net

  14. The Superstatistical Nature and Interoccurrence Time of Atmospheric Mercury Concentration Fluctuations

    Science.gov (United States)

    The probability density function (PDF) of the time intervals between subsequent extreme events in atmospheric Hg0 concentration data series from different latitudes has been investigated. The Hg0 dynamic possesses a long-term memory autocorrelation function. Above a fixed thresh...

  15. Response of archaeal communities in the rhizosphere of maize and soybean to elevated atmospheric CO2 concentrations.

    Directory of Open Access Journals (Sweden)

    David M Nelson

    Full Text Available BACKGROUND: Archaea are important to the carbon and nitrogen cycles, but it remains uncertain how rising atmospheric carbon dioxide concentrations ([CO(2] will influence the structure and function of soil archaeal communities. METHODOLOGY/PRINCIPAL FINDINGS: We measured abundances of archaeal and bacterial 16S rRNA and amoA genes, phylogenies of archaeal 16S rRNA and amoA genes, concentrations of KCl-extractable soil ammonium and nitrite, and potential ammonia oxidation rates in rhizosphere soil samples from maize and soybean exposed to ambient (∼385 ppm and elevated (550 ppm [CO(2] in a replicated and field-based study. There was no influence of elevated [CO(2] on copy numbers of archaeal or bacterial 16S rRNA or amoA genes, archaeal community composition, KCl-extractable soil ammonium or nitrite, or potential ammonia oxidation rates for samples from maize, a model C(4 plant. Phylogenetic evidence indicated decreased relative abundance of crenarchaeal sequences in the rhizosphere of soybean, a model leguminous-C(3 plant, at elevated [CO(2], whereas quantitative PCR data indicated no changes in the absolute abundance of archaea. There were no changes in potential ammonia oxidation rates at elevated [CO(2] for soybean. Ammonia oxidation rates were lower in the rhizosphere of maize than soybean, likely because of lower soil pH and/or abundance of archaea. KCl-extractable ammonium and nitrite concentrations were lower at elevated than ambient [CO(2] for soybean. CONCLUSION: Plant-driven shifts in soil biogeochemical processes in response to elevated [CO(2] affected archaeal community composition, but not copy numbers of archaeal genes, in the rhizosphere of soybean. The lack of a treatment effect for maize is consistent with the fact that the photosynthesis and productivity of maize are not stimulated by elevated [CO(2] in the absence of drought.

  16. Characteristics of permanganate oxidation of TCE at low reagent concentrations.

    Science.gov (United States)

    Woo, N C; Hyun, S G; Park, W W; Lee, E S; Schwartz, F W

    2009-12-01

    A controlled-release technique using potassium permanganate (KMnO4) has been recently developed as a long-term and semi-passive remediation scheme for dilute groundwater plumes of chlorinated solvents such as trichloroethylene (TCE) and perchloroethylene. Batch experiments were performed to evaluate TCE removal efficiencies of a low concentration of permanganate (MnO4-) solution and to estimate the optimum dose of permanganate required to remove low levels of TCE from groundwater plumes without leaving intermediate organic forms. Experimental results indicated that when the molar ratio of [MnO4-]0/[TCE]0 was about 10, 95% of the TCE in the plume was removed within less than 90 min, and about 90% of the chloride in the organic forms was converted into inorganic ions, while the TCE removal rates and the chloride conversion rates were considerably lower when the [TCE]0/ [MnO4-]0 values were lower. These data suggested that the [MnO4-]0 and the [MnO4-]0/[TCE]0 values would have strong effects on the efficiency and completeness of TCE oxidation. Further detailed investigations of the effect of [MnO4-]0 and [MnO4-]0/[TCE]0 values on the removal efficiencies and completeness of the TCE oxidation are warranted for successful application of the controlled-release KMnO4 technique in practice.

  17. Concentration-dependent toxicity of iron oxide nanoparticles mediated by increased oxidative stress

    Directory of Open Access Journals (Sweden)

    Saba Naqvi

    2010-11-01

    Full Text Available Saba Naqvi1, Mohammad Samim2, MZ Abdin3, Farhan Jalees Ahmed4, AN Maitra5, CK Prashant6, Amit K Dinda61Faculty of Engineering and Interdisciplinary Sciences, 2Department of Chemistry, 3Department of Biotechnology, Faculty of Science, 4Department of Pharmaceutics, Faculty of Pharmacy, Jamia Hamdard, Hamdard University, 5Department of Chemistry, University of Delhi, 6Department of Pathology, All India Institute of Medical Sciences, New Delhi, IndiaAbstract: Iron oxide nanoparticles with unique magnetic properties have a high potential for use in several biomedical, bioengineering and in vivo applications, including tissue repair, magnetic resonance imaging, immunoassay, drug delivery, detoxification of biologic fluids, cell sorting, and hyperthermia. Although various surface modifications are being done for making these nonbiodegradable nanoparticles more biocompatible, their toxic potential is still a major concern. The current in vitro study of the interaction of superparamagnetic iron oxide nanoparticles of mean diameter 30 nm coated with Tween 80 and murine macrophage (J774 cells was undertaken to evaluate the dose- and time-dependent toxic potential, as well as investigate the role of oxidative stress in the toxicity. A 15–30 nm size range of spherical nanoparticles were characterized by transmission electron microscopy and zeta sizer. MTT assay showed >95% viability of cells in lower concentrations (25–200 µg/mL and up to three hours of exposure, whereas at higher concentrations (300–500 µg/mL and prolonged (six hours exposure viability reduced to 55%–65%. Necrosis-apoptosis assay by propidium iodide and Hoechst-33342 staining revealed loss of the majority of the cells by apoptosis. H2DCFDDA assay to quantify generation of intracellular reactive oxygen species (ROS indicated that exposure to a higher concentration of nanoparticles resulted in enhanced ROS generation, leading to cell injury and death. The cell membrane injury

  18. Atmospheric alcohols and aldehydes concentrations measured in Osaka, Japan and in Sao Paulo, Brazil

    International Nuclear Information System (INIS)

    Nguyen, Ha Thi-Hoang; Takenaka, Norimichi; Bandow, Hiroshi; Maeda, Yasuaki; Oliva, S.T. de; Botelho, M.M.; Tavares, T.M.

    2001-01-01

    The use of alcohol fuel has received much attention since the 1980s. In Brazil, ethanol-fuelled vehicles have been currently used on a large scale. This paper reports the atmospheric methanol and isoproponal concentrations which were measured from May to December 1997, in Osaka, Japan, where alcohol fuel was not used and from 3 to 9 February 1998 in Sao Paulo, Brazil, where ethanol was used. The alcohols were determined by the alkyl nitrite formation reaction using gas chromatography (GC-ECD) analysis. The concentration of atmospheric alcohols, especially ethanol, measured in Sao Paulo were significantly higher than those in Osaka. In Osaka, the average concentrations of atmospheric methanol, ethanol, and isopropanol were 5.8 ± 3.8, 8.2 ± 4.6, and 7.2 ± 5.9ppbv, respectively. The average ambient levels of methanol, ethanol, and isopropanol measured in Sao Paulo were 34.1± 9.2, 176.3 ± 38.1, and 44.2 ± 13.7ppbv, respectively. The ambient levels of aldehydes, which were expected to be high due to the use of alcohol fuel, were also measured at these sampling sites. The atmospheric formaldehyde average measured in Osaka was 1.9± 0.9ppbv, and the average acetaldehyde concentration was 1.5 ± 0.8ppbv. The atmospheric formaldehyde and acetaldehyde average concentrations measured in Sao Paulo were 5.0 ± 2.8 and 5.4 ± 2.8ppbv, respectively. The C 2 H 5 OH/CH 3 OH and CH 3 CHO/HCHO were compared between the two measurement sites and elsewhere in the world, which have already been reported in the literature. Due to the use of ethanol-fuelled vehicles, these ratios, especially C-2H 5 OH/CH 3 OH, are much higher in Brazil than those measured elsewhere in the world. (Author)

  19. Relationships between Atmospheric Transport Regimes and PCB Concentrations in the Air at Zeppelin, Spitsbergen.

    Science.gov (United States)

    Ubl, Sandy; Scheringer, Martin; Hungerbühler, Konrad

    2017-09-05

    Polychlorinated biphenyls (PCBs) are persistent hazardous chemicals that are still detected in the atmosphere and other environmental media, although their production has been banned for several decades. At the long-term monitoring site, Zeppelin at Spitsbergen, different PCB congeners have been continuously measured for more than a decade. However, it is not clear what factors determine the seasonal and interannual variability of different (lighter versus heavier) PCB congeners. To investigate the influence of atmospheric transport patterns on PCB-28 and PCB-101 concentrations at Zeppelin, we applied the Lagrangian Particle Dispersion Model FLEXPART and calculated "footprints" that indicate the potential source regions of air arriving at Zeppelin. By means of a cluster analysis, we assigned groups of similar footprints to different transport regimes and analyzed the PCB concentrations according to the transport regimes. The concentrations of both PCB congeners are affected by the different transport regimes. For PCB-101, the origin of air masses from the European continent is primarily related to high concentrations; elevated PCB-101 concentrations in winter can be explained by the high frequency of this transport regime in winter, whereas PCB-101 concentrations are low when air is arriving from the oceans. For PCB-28, in contrast, concentrations are high during summer when air is mainly arriving from the oceans but low when air is arriving from the continents. The most likely explanation of this finding is that local emissions of PCB-28 mask the effect of long-range transport and determine the concentrations measured at Zeppelin.

  20. Oxidation of atmospheric methane in Northern European soils, comparison with other ecosystems, and uncertainties in the global terrestrial sink

    DEFF Research Database (Denmark)

    Smith, K.A.; Dobbie, K.E.; Ball, B.C.

    2000-01-01

    to the oxidation. The effect of temperature was small, attributed to substrate limitation and low atmospheric concentration. Analysis of all available data for CH4 oxidation rates in situ showed similar log-normal distributions to those obtained for our results, with generally little difference between different......This paper reports the range and statistical distribution of oxidation rates of atmospheric CH4 in soils found in Northern Europe in an international study, and compares them with published data for various other ecosystems. It reassesses the size, and the uncertainty in, the global terrestrial CH4...... sink, and examines the effect of land-use change and other factors on the oxidation rate. Only soils with a very high water table were sources of CH4; all others were sinks. Oxidation rates varied from 1 to nearly 200 µg CH4 m-2 h-1; annual rates for sites measured for =1 y were 0.1-9.1 kg CH4 ha-1 y-1...

  1. Variation of atmospheric 210Pb concentration in the inland area of Chinese continent

    International Nuclear Information System (INIS)

    Doi, Taeko; Sato, Jun.

    1995-01-01

    Atmospheric concentrations of 210 Pb and their variations over Urumqi, Lanzhou and Baotou, cities located in inland area of Chinese continent, were observed for a period of 1 year in 1992. The monthly average concentrations ranged from 0.27 to 4.57 mBq/m 3 . The concentrations over these cities in winter were several times higher than that observed at Tsukuba Science City, Japan, and the range of variation was also larger. The variations in concentration over the 3 localities were similar to each other, showing the same seasonal variation pattern: low concentration appeared in summer and high in winter. This variation pattern was different from that observed at Tsukuba Science City. The variations in concentration over Chinese continent, where precipitation is much lower than that in Japan, correlated quite well with the variation in precipitation. (author)

  2. Estimation of maximum credible atmospheric radioactivity concentrations and dose rates from nuclear tests

    International Nuclear Information System (INIS)

    Telegadas, K.

    1979-01-01

    A simple technique is presented for estimating maximum credible gross beta air concentrations from nuclear detonations in the atmosphere, based on aircraft sampling of radioactivity following each Chinese nuclear test from 1964 to 1976. The calculated concentration is a function of the total yield and fission yield, initial vertical radioactivity distribution, time after detonation, and rate of horizontal spread of the debris with time. calculated maximum credible concentrations are compared with the highest concentrations measured during aircraft sampling. The technique provides a reasonable estimate of maximum air concentrations from 1 to 10 days after a detonation. An estimate of the whole-body external gamma dose rate corresponding to the maximum credible gross beta concentration is also given. (author)

  3. Nitrogen concentrations in mosses indicate the spatial distribution of atmospheric nitrogen deposition in Europe

    International Nuclear Information System (INIS)

    Harmens, H.; Norris, D.A.; Cooper, D.M.; Mills, G.; Steinnes, E.; Kubin, E.; Thoeni, L.; Aboal, J.R.; Alber, R.; Carballeira, A.; Coskun, M.; De Temmerman, L.; Frolova, M.; Gonzalez-Miqueo, L.

    2011-01-01

    In 2005/6, nearly 3000 moss samples from (semi-)natural location across 16 European countries were collected for nitrogen analysis. The lowest total nitrogen concentrations in mosses ( 2 = 0.91) linear relationship was found between the total nitrogen concentration in mosses and measured site-specific bulk nitrogen deposition rates. The total nitrogen concentrations in mosses complement deposition measurements, helping to identify areas in Europe at risk from high nitrogen deposition at a high spatial resolution. - Highlights: → Nitrogen concentrations in mosses were determined at ca. 3000 sites across Europe. → Moss concentrations were compared with EMEP modelled nitrogen deposition. → The asymptotic relationship for Europe showed saturation at ca. 15 kg N ha -1 y -1 . → Linear relationships were found with measured nitrogen deposition in some countries. → Moss concentrations complement deposition measurements at high spatial resolution. - Mosses as biomonitors of atmospheric nitrogen deposition in Europe.

  4. RELATIONSHIP BETWEEN ATMOSPHERIC CO_2 AND CH_4 CONCENTRATIONS AT SYOWA STATION, ANTARCTICA

    OpenAIRE

    アオキ, シュウジ; ナカザワ, タカキヨ; ムラヤマ, ショウヘイ; シミズ, アキラ; ハヤシ, マサヒコ; イワイ, クニモト; Shuhji, AOKI; Takakiyo, NAKAZAWA; Shohei, MURAYAMA; Akira, SHIMIZU; Masahiko, HAYASHI; Kunimoto, IWAI

    1994-01-01

    Precise measurements of the atmospheric CO_2 and CH_4 concentrations have been continued at Syowa Station since 1984 and 1987,respectively. Measured concentrations show secular increase, together with seasonal cycle and irregular variations. Negative correlation is clearly seen between the secular trends of the CO_2 and CH_4 concentrations. The increase rates of CO_2 and CH_4 show oscillations with periods of 2.3 to 2.8 years. The phases of the average seasonal cycles of CO_2 and CH_4 coincid...

  5. Relationship between atmospheric ammonia concentration and nitrogen content in terricolous lichen (Cladonia portentosa)

    DEFF Research Database (Denmark)

    Nielsen, Knud Erik; Andersen, Helle Vibeke; Strandberg, Morten Tune

    2014-01-01

    From April 2006 to April 2007, the geographical and seasonal variation in nitrogen content in terricolous lichen (Cladonia portentosa) and atmospheric ammonia concentrations were measured at five heathland sites. The seasonal variation in the nitrogen content of the lichen was small, even though...... there was a large seasonal variation in the air concentration of ammonia. A sizable local variation in the nitrogen content of the lichen was found even at the scale of a few kilometres. The nitrogen content in the lichen showed a high correlation to the yearly mean value of the measured ammonia concentration...

  6. Results of long-term measurement of 222Rn concentrations in outdoor atmosphere

    International Nuclear Information System (INIS)

    Holy, K.; Boehm, R.; Polaskova, A.; Hola, O.

    1998-01-01

    Results are reported of the authors' long-term measurement of 222 Rn concentrations in the outdoor atmosphere. The measurements started in 1987 and were performed at a height of 1.5 m over a grass-covered ground surface, using till 1991 a Lucas type scintillation chamber and later a large volume scintillation chamber. Graphs are presented and discussed of the course of average monthly radon concentration in 1987-1996 and of annual courses of radon concentration for different time intervals of the day over 1991 to 1995. (A.K.)

  7. Investigation of Zirconium Oxide Films in Different Dissolved Hydrogen Concentration

    International Nuclear Information System (INIS)

    Kim, Taeho; Choi, Kyoung Joon; Yoo, Seung Chang; Kim, Ji Hyun

    2016-01-01

    It has been reported that in pre-transition zirconium oxide, the volume fraction of tetragonal zirconium oxide increased near the oxide/metal (O/M) interface, and the sub-stoichiometric zirconium oxide layer was observed. The diffusion of oxygen ion through the oxide layer is the rate-limiting process during the pre-transition oxidation process, and this diffusion mainly occurs in the grain boundaries. The two layered oxide structure is formed in pre-transition oxide for the zirconium alloy in high-temperature water environment. It is known that the corrosion rate is related to the volume fraction of zirconium oxide and the pores in the oxides; therefore, the aim of this paper is to investigate the oxidation behavior in the pre-transition zirconium oxide in high-temperature water chemistry. In this study, in situ Raman and TEM analysis were conducted for investigating the phase transformation of zirconium alloy in primary water. From this study, the following conclusions are drawn: 1. The zirconium alloy was oxidized in primary water chemistry for 100 d, and Raman and TEM were measured after 30, 50, 80, and 100 d from start-up. 2. TEM and FFT analysis showed that the zirconium oxide mostly consisted of the monoclinic phase. The tetragonal zirconium oxide was just found near the O/M interface

  8. An approach for verifying biogenic greenhouse gas emissions inventories with atmospheric CO2 concentration data

    International Nuclear Information System (INIS)

    Ogle, Stephen M; Davis, Kenneth; Lauvaux, Thomas; Miles, Natasha L; Richardson, Scott; Schuh, Andrew; Cooley, Dan; Breidt, F Jay; West, Tristram O; Heath, Linda S; Smith, James E; McCarty, Jessica L; Gurney, Kevin R; Tans, Pieter; Denning, A Scott

    2015-01-01

    Verifying national greenhouse gas (GHG) emissions inventories is a critical step to ensure that reported emissions data to the United Nations Framework Convention on Climate Change (UNFCCC) are accurate and representative of a country’s contribution to GHG concentrations in the atmosphere. Furthermore, verifying biogenic fluxes provides a check on estimated emissions associated with managing lands for carbon sequestration and other activities, which often have large uncertainties. We report here on the challenges and results associated with a case study using atmospheric measurements of CO 2 concentrations and inverse modeling to verify nationally-reported biogenic CO 2 emissions. The biogenic CO 2 emissions inventory was compiled for the Mid-Continent region of United States based on methods and data used by the US government for reporting to the UNFCCC, along with additional sources and sinks to produce a full carbon balance. The biogenic emissions inventory produced an estimated flux of −408 ± 136 Tg CO 2 for the entire study region, which was not statistically different from the biogenic flux of −478 ± 146 Tg CO 2 that was estimated using the atmospheric CO 2 concentration data. At sub-regional scales, the spatial density of atmospheric observations did not appear sufficient to verify emissions in general. However, a difference between the inventory and inversion results was found in one isolated area of West-central Wisconsin. This part of the region is dominated by forestlands, suggesting that further investigation may be warranted into the forest C stock or harvested wood product data from this portion of the study area. The results suggest that observations of atmospheric CO 2 concentration data and inverse modeling could be used to verify biogenic emissions, and provide more confidence in biogenic GHG emissions reporting to the UNFCCC. (letter)

  9. Nitrous Oxide Emissions from Biofuel Crops and Atmospheric Aerosols: Associations with Air Quality and Regional Climate

    Science.gov (United States)

    Pillai, Priya Ramachandran

    Emissions of greenhouse gases (GHG) and primary release and secondary formation of aerosols alter the earth's radiative balance and therefore have important climatic implications. Savings in carbon dioxide (CO2) emissions accomplished by replacing fossil fuels with biofuels may increase the nitrous oxide (N2O) emissions. Among various atmospheric trace gases, N2O, irrespective of its low atmospheric concentration, is the fourth most important gas in causing the global greenhouse effect. Major processes, those affect the concentration of atmospheric N2O, are soil microbial activities leading to nitrification and denitrification. Therefore, anthropogenic activities such as industrial emissions, and agricultural practices including application of nitrogenous fertilizers, land use changes, biomass combustion all contribute to the atmospheric N2O concentration. The emission rates of N2O related to biofuel production depend on the nitrogen (N) fertilizer uptake efficiency of biofuel crops. However, crops with less N demand, such as switchgrass may have more favorable climate impacts when compared to crops with high N demands, such as corn. Despite its wide environmental tolerance, the regional adaptability of the potential biofuel crop switch grass varies considerably. Therefore, it is important to regionally quantify the GHG emissions and crop yield in response to N-fertilization. A major objective of this study is to quantify soil emissions of N2O from switchgrass and corn fields as a function of N-fertilization. The roles of soil moisture and soil temperature on N2O fluxes were analyzed. These N2O observations may be used to parameterize the biogeochemical models to better understand the impact of different N2O emission scenarios. This study allows for improvements in climate models that focus on understanding the environmental impacts of the climate change mitigation strategy of replacing fossil fuels with biofuels. As a second major objective, the top of the

  10. Mechanical test of E110 cladding material oxidized in hydrogen rich steam atmosphere

    International Nuclear Information System (INIS)

    Windberg, P.; Perez-Fero, E.

    2005-01-01

    The behavior of the fuel cladding under accidental conditions has been studied at the AEKI for more than a decade. Earlier, the effect of oxygen and hydrogen content on the mechanical properties was studied separately. The present experiments can help to understand what kind of processes took place in the cleaning tank at Paks NPP (2003). The purpose of our experiments was to investigate high temperature oxidation of E110 cladding in steam + hydrogen mixture. A high temperature tube furnace was used for oxidation of the samples. The oxidation was carried out at three different temperatures (900 0 C, 1000 0 C, 1100 0 C). The hydrogen content in the steam was varied between 19-36 vol%. The oxygen content of the sample was defined as oxidation ratio. Two sizes (length: 2 and 8 mm) of cladding rings and 100 mm long E110 cladding tubes were oxidized. After the oxidation we made compression and tensile tests for rings, and ballooning experiments for 100 mm long tube. The most important conclusions were the following. Oxidation in H-rich steam atmosphere need longer time to get the same oxidation ratio compared to the steam oxidation without hydrogen. The shorter oxidation time results in a more compact oxide layer. The longer oxidation time leads to a cracked oxide layer. (author)

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

    International Nuclear Information System (INIS)

    Dang, Juan; Shi, Xiangli; Zhang, Qingzhu; Hu, Jingtian; Chen, Jianmin; Wang, Wenxing

    2014-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-08-15

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

  13. Metal concentrations in homing pigeon lung tissue as a biomonitor of atmospheric pollution.

    Science.gov (United States)

    Cui, Jia; Halbrook, Richard S; Zang, Shuying; Han, Shuang; Li, Xinyu

    2018-03-01

    Atmospheric pollution in urban areas is a major worldwide concern with potential adverse impacts on wildlife and humans. Biomonitoring can provide direct evidence of the bioavailability and bioaccumulation of toxic metals in the environment that is not available with mechanical air monitoring. The current study continues our evaluation of the usefulness of homing pigeon lung tissue as a biomonitor of atmospheric pollution. Homing pigeons (1-2, 5-6, and 9-10+ year old (yo)) collected from Guangzhou during 2015 were necropsied and concentrations of cadmium (Cd), lead (Pb), and mercury (Hg) were measured in lung tissue. Lung Cd and Pb concentrations were significantly greater in 9-10+-year-old pigeons compared with those in other age groups, indicating their bioavailability and bioaccumulation. Lung Pb and Cd concentrations measured in 5-yo pigeons collected from Guangzhou during 2015 were significantly lower than concentrations reported in 5-yo homing pigeons collected from Guangzhou during 2011 and correlated with concentrations measured using mechanical air monitoring. In addition to temporal differences, spatial differences in concentrations of Cd, Pb, and Hg reported in ambient air samples and in pigeon lung tissues collected from Beijing and Guangzhou are discussed.

  14. Seasonal trends in vegetation and atmospheric concentrations of PAHs and PBDEs near a sanitary landfill

    Science.gov (United States)

    St-Amand, Annick D.; Mayer, Paul M.; Blais, Jules M.

    Spruce needle and atmospheric (gaseous and particulate-bound) concentrations were surveyed near a sanitary landfill from February 2004 to June 2005. The influence of several parameters such as temperature, relative humidity, wind speed and direction, as well as increased domestic heating during the winter was assessed. In general, polybrominated diphenyl ethers (PBDE) and polycyclic aromatic hydrocarbons (PAH) concentrations in spruce needles increased over time and decreased following snowmelt with a minimum coinciding with bud burst of deciduous trees. Atmospheric concentrations of PBDE and PAH, both particulate-bound and gaseous phase, were linked to daily weather events and thus showed more variability than those in spruce needles. Highest PAH concentrations were encountered during the winter, likely reflecting increased emission from heating homes. Pseudo Clausius-Clapeyron plots revealed higher PBDE gaseous concentrations with increasing temperature, but showed no correlation between PAH gaseous concentrations and temperature as this effect was obscured by seasonal emission patterns. Finally, air mass back trajectories and local wind directions revealed that particulate-bound PBDEs, along with both gaseous and particulate-bound PAHs were from local sources, whereas gaseous PBDEs were likely from distant sources.

  15. A terrestrial biosphere model optimized to atmospheric CO2 concentration and above ground woody biomass

    Science.gov (United States)

    Saito, M.; Ito, A.; Maksyutov, S. S.

    2013-12-01

    This study documents an optimization of a prognostic biosphere model (VISIT; Vegetation Integrative Similator for Trace gases) to observations of atmospheric CO2 concentration and above ground woody biomass by using a Bayesian inversion method combined with an atmospheric tracer transport model (NIES-TM; National Institute for Environmental Studies / Frontier Research Center for Global Change (NIES/FRCGC) off-line global atmospheric tracer transport model). The assimilated observations include 74 station records of surface atmospheric CO2 concentration and aggregated grid data sets of above ground woody biomass (AGB) and net primary productivity (NPP) over the globe. Both the biosphere model and the atmospheric transport model are used at a horizontal resolution of 2.5 deg x 2.5 deg grid with temporal resolutions of a day and an hour, respectively. The atmospheric transport model simulates atmospheric CO2 concentration with nine vertical levels using daily net ecosystem CO2 exchange rate (NEE) from the biosphere model, oceanic CO2 flux, and fossil fuel emission inventory. The models are driven by meteorological data from JRA-25 (Japanese 25-year ReAnalysis) and JCDAS (JMA Climate Data Assimilation System). Statistically optimum physiological parameters in the biosphere model are found by iterative minimization of the corresponding Bayesian cost function. We select thirteen physiological parameter with high sensitivity to NEE, NPP, and AGB for the minimization. Given the optimized physiological parameters, the model shows error reductions in seasonal variation of the CO2 concentrations especially in the northern hemisphere due to abundant observation stations, while errors remain at a few stations that are located in coastal coastal area and stations in the southern hemisphere. The model also produces moderate estimates of the mean magnitudes and probability distributions in AGB and NPP for each biome. However, the model fails in the simulation of the terrestrial

  16. Subcooled flow boiling heat transfer of dilute alumina, zinc oxide, and diamond nanofluids at atmospheric pressure

    International Nuclear Information System (INIS)

    Kim, Sung Joong; McKrell, Tom; Buongiorno, Jacopo; Hu Linwen

    2010-01-01

    A nanofluid is a colloidal suspension of nano-scale particles in water, or other base fluids. Previous pool boiling studies have shown that nanofluids can improve the critical heat flux (CHF) by as much as 200%. In a previous paper, we reported on subcooled flow boiling CHF experiments with low concentrations of alumina, zinc oxide, and diamond nanoparticles in water (≤0.1% by volume) at atmospheric pressure, which revealed a substantial CHF enhancement (∼40-50%) at the highest mass flux (G = 2500 kg/m 2 s) and concentration (0.1 vol.%) for all nanoparticle materials (). In this paper, we focus on the flow boiling heat transfer coefficient data collected in the same tests. It was found that for comparable test conditions the values of the nanofluid and water heat transfer coefficient are similar (within ±20%). The heat transfer coefficient increased with mass flux and heat flux for water and nanofluids alike, as expected in flow boiling. A confocal microscopy-based examination of the test section revealed that nanoparticle deposition on the boiling surface occurred during nanofluid boiling. Such deposition changes the number of micro-cavities on the surface, but also changes the surface wettability. A simple model was used to estimate the ensuing nucleation site density changes, but no definitive correlation between the nucleation site density and the heat transfer coefficient data could be found.

  17. Effect of Grinding at Modified Atmosphere or Vacuum on Browning, Antioxidant Capacities, and Oxidative Enzyme Activities of Apple.

    Science.gov (United States)

    Kim, Ah-Na; Lee, Kyo-Yeon; Kim, Hyun-Jin; Chun, Jiyeon; Kerr, William L; Choi, Sung-Gil

    2018-01-01

    This study evaluated the effects of grinding at atmospheric pressure (control), under vacuum (∼2.67 kPa), or with modified atmosphere (N 2 and CO 2 ) on the browning, antioxidant activity, phenolics, and oxidative enzyme activity of apples as a function of time. The control group was affected most, showing distinct browning and losing most of the antioxidant activity and concentrations of the main phenolic compounds. The modified atmosphere groups retained color, antioxidant activity, and phenolic compounds better than the control group. Least changes were obtained with vacuum grinding, particularly in terms of preventing enzymatic browning and oxidation of antioxidants apples. At 12 h after grinding, vacuum-ground apples retained total phenolic contents 5.32, 1.54, and 1.49 times higher than control, nitrogen gas, and carbon dioxide gas-ground samples, respectively. The oxidative enzyme activity, including that of polyphenol oxidase and peroxidase, decreased in the control and modified atmosphere group, but they were maintained in the samples ground under the vacuum. In this study, we found that grinding with modified atmosphere or vacuum conditions could effectively prevent browning as well as loss of phenolic compounds and antioxidant activity of ground apples. These results can help scientists and engineers build better grinding systems for retaining nutrient and quality factors of ground apples. In addition, these results may be useful to other fruit and vegetable industries that wish to retain fresh-like quality and nutritional value during grinding and storage. © 2017 Institute of Food Technologists®.

  18. Relative effects of climate and source strength on atmospheric lead concentrations in Auckland, New Zealand

    Science.gov (United States)

    Power, H. C.; de Freitas, C. R.; Hay, J. E.

    1992-06-01

    Atmospheric lead levels were examined to assess the consequences of the 46 percent reduction in the lead content of premium grade petrol in New Zealand. Since this change was implemented in July 1986 observed levels of atmospheric lead decreased by 38 percent, but all or part of this reduction may have been due to factors other than fluctuations in lead emissions, notably variations in climate. Analysis of detailed atmospheric lead, meteorological and traffic data measured contemporaneously provided insight into the atmospheric processes influencing lead levels in Auckland and formed the basis of a statistical model capable of predicting monthly lead concentrations. The model was used to predict lead levels in Auckland for the period July 1986 through to July 1989 in the absence of any reduction in the lead content of petrol. Comparison with values observed for the same period showed that all of the reduction in atmospheric lead levels since July 1986 can be attributed to the reduction in the lead content of petrol. Policy planning implications of such a finding are considered.

  19. Analysis of Co, Cr and Mn Concentrations in Atmospheric Dry Deposition in Hamadan City

    Directory of Open Access Journals (Sweden)

    P. Shokri Ragheb

    2016-07-01

    Full Text Available Introduction & Objective: Heavy metals are major pollutants that can spread in the atmosphere with particulate matter and dust and because of the toxic and carcinogenic effects, their meas-urement and control is very important. Therefore, this study was conducted to assess Co, Cr and Mn concentration in the atmospheric dry deposition collected from Hamadan city in 2014. Materials & Methods: After collection of 12 dust samples from 3 sampling stations and their laboratory preparation, metals concentrations were determined using ICP–OES. All statistical analyses were performed using the SPSS statistical package. Results: The results showed that the minimum and maximum mean concentrations of Co were 0.19 and 0.29 mg/kg for high and low traffic intensity sampling stations, respectively. The min and max mean concentrations of Cr were 0.65and 1.02 mg/kg for high traffic intensity and suburb sampling stations, respectively and the min and max mean concentrations of Mn were 7.23and 8.82 mg/kg for high and low traffic intensity sampling stations , respectively. Also comparing the mean concentrations of assessed metals with WHO permissible limits showed a significant difference (P< 0.05. The mean concentrations of metals were signifi-cantly lower than the maximum permissible limits. Conclusion: Although the mean concentrations of Co, Cr and Mn are lower than the standard levels, lack of continuous monitoring of heavy metals concentrations in the dust and particu-late matters in the air can lead to the entrance of various types of toxic pollutants such as heavy metals into the air and result in adverse health effects. (Sci J Hamadan Univ Med Sci 2016; 23 (2:149-156

  20. Degradation of polyethylene induced by plasma in oxidizing atmospheres

    International Nuclear Information System (INIS)

    Colin, E.; Olayo, M.G.; Cruz, G.J.

    2002-01-01

    The garbage of polyethylene is not easily degradable in normal environmental conditions . The indiscriminate use of this polymer and the enormous quantity of garbage which is generated carries a damage to the environment due to its long life as waste. The objective of this work is to study the conditions in which can be carried out the degradation of polyethylene. A form of accelerating the degradation is exposing it to plasma with reactive atmospheres. In this work a study of surface modification of polyethylene by plasmas with discharges of direct current of oxygen and nitrogen is presented. (Author)

  1. Analysis of atmospheric concentrations of radon and thoron using beta counting technique

    International Nuclear Information System (INIS)

    Islam, G.S.; Basunia, S.M.

    1995-05-01

    This paper presents a detailed theory and experimental procedure for measurement and analysis of mixed radon and thoron in the environment. The technique has been successfully applied to the study of seasonal variations of radon and thoron in Rajshahi atmosphere during the years 1989-1991. The maximum radon concentration in outdoor air was observed in the winter from December to January while the indoor radon concentration was found to be maximum during the monsoon months of July and August. The implication of results is briefly discussed in the paper. (author). 4 refs, 6 figs, 2 tabs

  2. Concentration of 7Be in the lower atmosphere and fallout rate in Tokai

    International Nuclear Information System (INIS)

    Amano, Hikaru; Kasai, Atsushi

    1981-01-01

    Beryllium-7, cosmic ray produced radioactivity, its monthly average concentration in the lower atmosphere and monthly fallout rate were measured in Tokai, Japan. Then, the monthly variations were compared with those of fission products due to nuclear detonations in the atmosphere. The concentration of 7 Be in the lower atmosphere ranged from 0.5 x 10 -1 pCi/m 3 to 2.5 x 10 -1 pCi/m 3 in Tokai between the observed period, 1975 - 1977. The fallout rate of 7 Be vibrated widely, its range was from the detection limits to 1.2 x 10 4 pCi/m 2 . The monthly variations were not always the same with variations of the fission products. Fallout rate of 7 Be depended on the rain strongly. The concentration of 7 Be in the rain was measured, too. Then the range was from 9.2 pCi/l to 1.9 x 10 2 pCi/l between the observed period 1976.9 - 1977.2. (author)

  3. Technical Note: Long-term memory effect in the atmospheric CO2 concentration at Mauna Loa

    Directory of Open Access Journals (Sweden)

    C. Varotsos

    2007-01-01

    Full Text Available The monthly mean values of the atmospheric carbon dioxide concentration derived from in-situ air samples collected at Mauna Loa Observatory, Hawaii, USA during 1958–2004 (the longest continuous record available in the world are analyzed by employing the detrended fluctuation analysis to detect scaling behavior in this time series. The main result is that the fluctuations of carbon dioxide concentrations exhibit long-range power-law correlations (long memory with lag times ranging from four months to eleven years, which correspond to 1/f noise. This result indicates that random perturbations in the carbon dioxide concentrations give rise to noise, characterized by a frequency spectrum following a power-law with exponent that approaches to one; the latter shows that the correlation times grow strongly. This feature is pointing out that a correctly rescaled subset of the original time series of the carbon dioxide concentrations resembles the original time series. Finally, the power-law relationship derived from the real measurements of the carbon dioxide concentrations could also serve as a tool to improve the confidence of the atmospheric chemistry-transport and global climate models.

  4. Short-Chain Chlorinated Paraffins in Zurich, Switzerland--Atmospheric Concentrations and Emissions.

    Science.gov (United States)

    Diefenbacher, Pascal S; Bogdal, Christian; Gerecke, Andreas C; Glüge, Juliane; Schmid, Peter; Scheringer, Martin; Hungerbühler, Konrad

    2015-08-18

    Short-chain chlorinated paraffins (SCCPs) are of concern due to their potential for adverse health effects, bioaccumulation, persistence, and long-range transport. Data on concentrations of SCCPs in urban areas and underlying emissions are still scarce. In this study, we investigated the levels and spatial distribution of SCCPs in air, based on two separate, spatially resolved sampling campaigns in the city of Zurich, Switzerland. SCCP concentrations in air ranged from 1.8 to 17 ng·m(-3) (spring 2011) and 1.1 to 42 ng·m(-3) (spring 2013) with medians of 4.3 and 2.7 ng·m(-3), respectively. Both data sets show that atmospheric SCCP levels in Zurich can vary substantially and may be influenced by a number of localized sources within this urban area. Additionally, continuous measurements of atmospheric concentrations performed at one representative sampling site in the city center from 2011 to 2013 showed strong seasonal variations with high SCCP concentrations in summer and lower levels in winter. A long-term dynamic multimedia environmental fate model was parametrized to simulate the seasonal trends of SCCP concentrations in air and to back-calculate urban emissions. Resulting annual SCCP emissions in the city of Zurich accounted for 218-321 kg, which indicates that large SCCP stocks are present in urban areas of industrialized countries.

  5. Detection of atmospheric tritium by scintillation. Variations in its concentration in France

    International Nuclear Information System (INIS)

    Bibron, R.

    1964-06-01

    The tritium released into the atmosphere as a result of the explosion of thermonuclear devices is a useful radioactive tracer for the study of certain geophysical problems. The low concentrations found however call for the use of extremely sensitive detectors. Two detection methods using liquid scintillators are described. In the first method, the sample is introduced into the scintillator in liquid form, after prior concentration of the tritium by electrolysis. In the second method the tritium is incorporated into the scintillator solvent molecule by chemical synthesis. In the last part of the report are examined the variations in the tritium concentration in rain-water and of the free hydrogen in the air in France. A discussion is then made of the seasonal variations in the case of rain-water and these are compared to the variations in the strontium-90 concentrations. (author) [fr

  6. Temporal variations in elemental concentrations of atmospheric aerosols in Mexico City

    International Nuclear Information System (INIS)

    Aldape U, F.

    1992-05-01

    Measurements are reported of elemental concentrations of airborne particulates in Mexico City and their time variation over a one-week period in the spring of 1988. Proton-induced X-ray emission analysis, PIXE, was used to analyse the atmospheric aerosols which were bombarded with 2.5 MeV protons from the 12 MV Tandem Van de Graaff accelerator at the National Institute of Nuclear Research, ININ. Variations in the elemental concentrations were observed over the time period studied. An intercomparison was made in the case of the element lead with PIXE results obtained at the Crocker Nuclear Laboratory, CNL, University of California for the same set of samples. Excellent agreement was obtained both for the time variation of the relative concentration and the absolute lead concentrations. These results give added confidence to the protocol adopted at ININ. (Author)

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

    Science.gov (United States)

    Dang, Juan; Shi, Xiangli; Zhang, Qingzhu; Hu, Jingtian; Chen, Jianmin; Wang, Wenxing

    2014-08-15

    The atmospheric oxidation of polycyclic aromatic hydrocarbons (PAHs) can generate toxic derivatives which contribute to the carcinogenic potential of particulate organic matter. In this work, the mechanism of the OH-initiated atmospheric oxidation of fluoranthene (Flu) was investigated by using high-accuracy molecular orbital calculations. All of the possible oxidation pathways were discussed, and the theoretical results were compared with the available experimental observation. The rate constants of the crucial elementary reactions were evaluated by the Rice-Ramsperger-Kassel-Marcus (RRKM) theory. The main oxidation products are a range of ring-retaining and ring-opening chemicals containing fluoranthols, fluoranthones, fluoranthenequinones, nitro-fluoranthenes, dialdehydes and epoxides. The overall rate constant of the OH addition reaction is 1.72×10(-11) cm(3) molecule(-1) s(-1) at 298 K and 1 atm. The atmospheric lifetime of Flu determined by OH radicals is about 0.69 days. This work provides a comprehensive investigation of the OH-initiated oxidation of Flu and should help to clarify its atmospheric conversion. Copyright © 2014 Elsevier B.V. All rights reserved.

  8. Interaction of oxides of nitrogen and aromatic hydrocarbons under simulated atmospheric conditions

    International Nuclear Information System (INIS)

    Obrien, R.J.; Green, P.J.; Doty, R.A.; Vanderzanden, J.W.; Easton, R.R.; Irwin, R.P.

    1979-01-01

    The reactions of nitrogen oxides with aromatic hydrocarbons under simulated atmospheric conditions are investigated. Gaseous reaction products formed when toluene is irradiated under simulated atmospheric conditions in the presence of nitrogen oxides were analyzed by gas chromatography. Reaction products detected include acetylene, water, acetaldehyde, acetone, toluene, benzaldehyde, ortho-, meta- and para-cresol, benzyl nitrate and meta- and para-nitrotoluene. Reaction mechanisms yielding the various products are illustrated. The assumption that all the nitrogen oxides observed to be lost from the reaction products can be accounted for by nitric acid formation in the absence of ozone formation is verified by a model in which the hydroxyl radical is assumed to be the only means of removing toluene. Under conditions in which ozone is formed, nitrogen oxide loss is accounted for by ozone formation in addition to nitric acid formation

  9. Development of a 10 Hz measurement system for atmospheric aerosol concentration

    International Nuclear Information System (INIS)

    Bouarouri, Assia

    2014-01-01

    The goal is to develop an aerosol charger based on a corona discharge for atmospheric concentration measurements (10 3 -10 5 cm -3 ) within a response time of 100 ms. Two ion sources, point-to-hole and wire-to-slit have been characterized. The increase of the ion flow in the post-discharge by EHD ion confinement in both the discharge gap and the hole has been shown. At first, using an experimental survey driven in two mixing configurations, concentric and face-to-face, we have confirmed the aerosol diffusion charging law which depends on aerosol diameter and N i .t product, with N i , the ions concentration and t, the charging time. Thus, the originality of this charger relies on the very high heterogeneity of unipolar ion densities (N i 0 ≥10 9 cm -3 ) required to compensate the charging time of 50 ms. In these conditions, we have shown that aerosol diameter and the charging dynamic (which depends also on the diameter) control the aerosol trajectory. The chargers have, next, been compared in different operating conditions, mainly in terms of the maximal charging and the minimal losses. In the chosen charger (point-to-hole ion source and concentric mixing), the relations charge/mobility and losses according to diameter have been characterized. We have also shown the linearity of the charged particles current with the aerosol concentration which allows the current-concentration data inversion. The preliminary measurement system composed by the charger, the separator and the particle current measurements, satisfies the objectives of the study in terms of the concentration detection limit (10 3 cm -3 ) and the response time (100 ms). We have thus shown the feasibility of an atmospheric aerosol concentration measurement system at 10 Hz using a corona discharge charger provided that the separation power is improved. Furthermore, knowing that aerosol losses are negligible and the lower limit of the partial charging, the developed charger is adaptable with other

  10. Correlation between meteorological conditions and the concentration of radionuclides in the ground layer of atmospheric air

    International Nuclear Information System (INIS)

    Krajny, E.; Osrodka, L.; Wojtylak, M.; Michalik, B.; Skowronek, J.

    2001-01-01

    The main goal of this work was to find correlation between the concentrations of radionuclides in outdoor air and the meteorological conditions like: atmospheric pressure, wind velocity and amount of precipitation. Because the sampling period of radionuclides concentrations in air was relatively long (7 days), the average levels of meteorological parameters have been calculated within the same time. Data of radionuclide concentrations and meteorological data have been analyzed in order to find statistical correlation. The regression analysis and one of AI methods, known as neural network, were applied. In general, analysis of the gathered data does not show any strong correlation between the meteorological conditions and the concentrations of the radionuclides in air. A slightly stronger correlation we found for radionuclides with relatively short half-lives. The only positive correlation has been found between the 7 Be concentration and air temperature (at the significance level α = 0.05). In our opinion, the lack of correlation was caused by a too long sampling time in measurements of radionuclides in outdoor air (a whole week). Results of analysis received by means of the artificial neuron network are better. We were able to find certain groups of meteorological conditions, related with the corresponding concentrations of particular radionuclides in air. Preliminary measurements of radon progeny concentration support the thesis that the link between changes of meteorological parameters and concentrations of radionuclides in ambient air must exist. (author)

  11. Nitrogen concentrations in mosses indicate the spatial distribution of atmospheric nitrogen deposition in Europe

    Energy Technology Data Exchange (ETDEWEB)

    Harmens, H., E-mail: hh@ceh.ac.uk [Centre for Ecology and Hydrology, Environment Centre Wales, Deiniol Road, Bangor, Gwynedd LL57 2UW (United Kingdom); Norris, D.A., E-mail: danor@ceh.ac.uk [Centre for Ecology and Hydrology, Environment Centre Wales, Deiniol Road, Bangor, Gwynedd LL57 2UW (United Kingdom); Cooper, D.M., E-mail: cooper@ceh.ac.uk [Centre for Ecology and Hydrology, Environment Centre Wales, Deiniol Road, Bangor, Gwynedd LL57 2UW (United Kingdom); Mills, G., E-mail: gmi@ceh.ac.uk [Centre for Ecology and Hydrology, Environment Centre Wales, Deiniol Road, Bangor, Gwynedd LL57 2UW (United Kingdom); Steinnes, E., E-mail: Eiliv.Steinnes@chem.ntnu.no [Department of Chemistry, Norwegian University of Science and Technology, 7491 Trondheim (Norway); Kubin, E., E-mail: Eero.Kubin@metla.fi [Finnish Forest Research Institute, Kirkkosaarentie 7, 91500 Muhos (Finland); Thoeni, L., E-mail: lotti.thoeni@fub-ag.ch [FUB-Research Group for Environmental Monitoring, Alte Jonastrasse 83, 8640 Rapperswil (Switzerland); Aboal, J.R., E-mail: jesusramon.aboal@usc.es [University of Santiago de Compostela, Faculty of Biology, Department of Ecology, 15782 Santiago de Compostela (Spain); Alber, R., E-mail: Renate.Alber@provinz.bz.it [Environmental Agency of Bolzano, 39055 Laives (Italy); Carballeira, A., E-mail: alejo.carballeira@usc.es [University of Santiago de Compostela, Faculty of Biology, Department of Ecology, 15782 Santiago de Compostela (Spain); Coskun, M., E-mail: coskunafm@yahoo.com [Canakkale Onsekiz Mart University, Faculty of Medicine, Department of Medical Biology, 17100 Canakkale (Turkey); De Temmerman, L., E-mail: ludet@var.fgov.be [Veterinary and Agrochemical Research Centre, Tervuren (Belgium); Frolova, M., E-mail: marina.frolova@lvgma.gov.lv [Latvian Environment, Geology and Meteorology Agency, Riga (Latvia); Gonzalez-Miqueo, L., E-mail: lgonzale2@alumni.unav.es [Univ. of Navarra, Irunlarrea No 1, 31008 Pamplona (Spain)

    2011-10-15

    In 2005/6, nearly 3000 moss samples from (semi-)natural location across 16 European countries were collected for nitrogen analysis. The lowest total nitrogen concentrations in mosses (<0.8%) were observed in northern Finland and northern UK. The highest concentrations ({>=}1.6%) were found in parts of Belgium, France, Germany, Slovakia, Slovenia and Bulgaria. The asymptotic relationship between the nitrogen concentrations in mosses and EMEP modelled nitrogen deposition (averaged per 50 km x 50 km grid) across Europe showed less scatter when there were at least five moss sampling sites per grid. Factors potentially contributing to the scatter are discussed. In Switzerland, a strong (r{sup 2} = 0.91) linear relationship was found between the total nitrogen concentration in mosses and measured site-specific bulk nitrogen deposition rates. The total nitrogen concentrations in mosses complement deposition measurements, helping to identify areas in Europe at risk from high nitrogen deposition at a high spatial resolution. - Highlights: > Nitrogen concentrations in mosses were determined at ca. 3000 sites across Europe. > Moss concentrations were compared with EMEP modelled nitrogen deposition. > The asymptotic relationship for Europe showed saturation at ca. 15 kg N ha{sup -1} y{sup -1}. > Linear relationships were found with measured nitrogen deposition in some countries. > Moss concentrations complement deposition measurements at high spatial resolution. - Mosses as biomonitors of atmospheric nitrogen deposition in Europe.

  12. Oxidation behavior of stainless steel 430 and 441 at 800 C in single (air/air) and dual atmosphere (air/hydrogen) exposures

    Energy Technology Data Exchange (ETDEWEB)

    Rufner, J.; Gannon, P.; White, P.; Deibert, M.; Teintze, S. [Chemical and Biological Engineering, Montana State University, 306 Cobleigh Hall, Bozeman, MT 59717-3920 (United States); Smith, R.; Chen, H. [Physics, Montana State University, 306 Cobleigh Hall, Bozeman, MT 59717-3920 (United States)

    2008-02-15

    Intermediate temperature ({proportional_to}800 {sup o}C) planar solid oxide fuel cells (SOFCs) allow the use of ferritic stainless steel (FSS) interconnects. SOFC FSS interconnects are used to stack individual cells into series, and are simultaneously exposed to air on the cathode side and fuel on the anode side, creating a 'dual atmosphere' exposure. The thermally grown oxide (TGO) layers on the air side of FSSs 430 and 441 were analyzed as a function of simulated dual atmosphere exposures (moist air/moist hydrogen) for up to 300 h. FSS 430 showed some changes in oxidation behavior, with a slight Fe concentration increase and localized Fe{sub 2}O{sub 3} nodule formation observed in the dual atmosphere TGO layer relative to its single atmosphere (air/air) counterpart. Significantly accelerated and anomalous oxidation was observed with FSS 441 subjected to dual atmosphere exposures compared with air/air exposures. The TGO layer formed on the 441 exposed to air/air was comprised of Mn-rich, Cr and Fe-containing isomorphic spinel surface crystallites, with a Cr{sub 2}O{sub 3} (eskolaite)-based bottom layer, having a total TGO layer thickness of <2{mu} m after 300 h. In contrast, the TGO layer formed on 441 during dual atmosphere exposure was much faster-growing (>6{mu} m in 20 h) and exhibited a continuous, porous Fe{sub 2}O{sub 3}-rich surface layer with a relatively thin (<2{mu} m) sublayer of similar composition to the TGO layer formed during the air/air exposure. Spontaneous TGO layer spallation was also observed for the air side of 441 exposed to dual atmosphere for >100h. The observed oxidation behavior and TGO layer evolution of 441 in both air/air and dual atmosphere are presented, with possible mechanisms and implications discussed. (author)

  13. Fog composition at Baengnyeong Island in the eastern Yellow Sea: detecting markers of aqueous atmospheric oxidations

    Directory of Open Access Journals (Sweden)

    A. J. Boris

    2016-01-01

    Full Text Available Samples of fog water were collected at Baengnyeong Island (BYI in the Yellow Sea during the summer of 2014. The most abundant chemical species in the fog water were NH4+ (mean of 2220 µM, NO3− (1260 µM, SO4−2 (730 µM, and Na+ (551 µM, with substantial contributions from other species consistent with marine and biomass burning influence on some dates. The pH of the samples ranged between 3.48 and 5.00, with a mean of 3.94, intermediate within pH values of fog/cloud water reported previously in Southeast Asia. Back trajectories (72 h showed that high relative humidity ( >  80 % was encountered upwind of the sampling site by all but one of the sampled air masses, and that the fog composition at BYI can be impacted by several different source regions, including the Sea of Japan, southeastern China, northeastern China, and the East China Sea. Sulfur in the collected fog was highly oxidized: low S(IV concentrations were measured (mean of 2.36 µM in contrast to SO4−2 and in contrast to fog/cloud S(IV concentrations from pollutant source regions; organosulfate species were also observed and were most likely formed through aging of mainly biogenic volatile organic compounds. Low-molecular-mass organic acids were major contributors to total organic carbon (TOC; 36–69 %, comprising a fraction of TOC at the upper end of that seen in fogs and clouds in other polluted environments. Large contributions were observed from not only acetic and formic acids but also oxalic, succinic, maleic, and other organic acids that can be produced in aqueous atmospheric organic processing (AAOP reactions. These samples of East Asian fog water containing highly oxidized components represent fog downwind of pollutant sources and can provide new insight into the fate of regional emissions. In particular, these samples demonstrate the result of extensive photochemical aging during multiday transport, including oxidation within wet aerosols and

  14. Fog composition at Baengnyeong Island in the eastern Yellow Sea: detecting markers of aqueous atmospheric oxidations

    Science.gov (United States)

    Boris, A. J.; Lee, T.; Park, T.; Choi, J.; Seo, S. J.; Collett, J. L., Jr.

    2016-01-01

    Samples of fog water were collected at Baengnyeong Island (BYI) in the Yellow Sea during the summer of 2014. The most abundant chemical species in the fog water were NH4+ (mean of 2220 µM), NO3- (1260 µM), SO4-2 (730 µM), and Na+ (551 µM), with substantial contributions from other species consistent with marine and biomass burning influence on some dates. The pH of the samples ranged between 3.48 and 5.00, with a mean of 3.94, intermediate within pH values of fog/cloud water reported previously in Southeast Asia. Back trajectories (72 h) showed that high relative humidity ( > 80 %) was encountered upwind of the sampling site by all but one of the sampled air masses, and that the fog composition at BYI can be impacted by several different source regions, including the Sea of Japan, southeastern China, northeastern China, and the East China Sea. Sulfur in the collected fog was highly oxidized: low S(IV) concentrations were measured (mean of 2.36 µM) in contrast to SO4-2 and in contrast to fog/cloud S(IV) concentrations from pollutant source regions; organosulfate species were also observed and were most likely formed through aging of mainly biogenic volatile organic compounds. Low-molecular-mass organic acids were major contributors to total organic carbon (TOC; 36-69 %), comprising a fraction of TOC at the upper end of that seen in fogs and clouds in other polluted environments. Large contributions were observed from not only acetic and formic acids but also oxalic, succinic, maleic, and other organic acids that can be produced in aqueous atmospheric organic processing (AAOP) reactions. These samples of East Asian fog water containing highly oxidized components represent fog downwind of pollutant sources and can provide new insight into the fate of regional emissions. In particular, these samples demonstrate the result of extensive photochemical aging during multiday transport, including oxidation within wet aerosols and fogs.

  15. Possible future scenarios for atmospheric concentration of greenhouse gases. A simplified thermodynamic approach

    International Nuclear Information System (INIS)

    Angulo-Brown, F.; Sanchez-Salas, N.; Barranco-Jimenez, M.A.; Rosales, M.A.

    2009-01-01

    Most of the increase in concentrations of greenhouse gases in the Earth's atmosphere is mainly due to anthropogenic activities. This is particularly significant in the case of CO 2 . The atmospheric concentration of CO 2 has systematically increased since the Industrial Revolution (260 ppm), with a remarkable raise after the 1970s until the present day (380 ppm). If this increasing tendency is maintained, the last report of the Intergovernmental Panel on Climate Change (IPCC) estimates that, for the year 2100, the CO 2 concentration can augment up to approximately 675 ppm. In this work it is assumed that the quantity of anthropogenic greenhouse gases emitted to the Earth's atmosphere is proportional to the quantity of heat rejected to the environment by internal combustion heat engines. It is also assumed that this increasing tendency of CO 2 due to men's activity stems from a mode of energy production mainly based on a maximum-power output paradigm. With these hypotheses, a thermoeconomic optimization of a thermal engine model under two regimes of performance: the maximum-power regime and the so-called ecological function criterion is presented. This last regime consists in maximizing a function that represents a good compromise between high power output and low entropy production. It is showed that, under maximum ecological conditions, the emissions of thermal energy to the environment are reduced approximately up to 50%. Thus working under this mode of performance the slope of the curves of CO 2 concentration, for instance, drastically diminishes. A simple qualitative criterion to design ecological taxes is also suggested. (author)

  16. Atmospheric concentrations of organochlorine pesticides, polybrominated diphenyl ethers and polychloronaphthalenes in Nuuk, South-West Greenland

    Science.gov (United States)

    Bossi, Rossana; Skov, Henrik; Vorkamp, Katrin; Christensen, Jesper; Rastogi, Suresh C.; Egeløv, Axel; Petersen, Dorthe

    Atmospheric concentrations of organochlorine pesticides (OCs), polybrominated diphenyl ethers (PBDEs) and polychloronaphthalenes (PCNs) were measured for the first time in Nuuk, Greenland in 2004 and 2005. The annual mean concentrations of the measured OCs were: α-HCH 20.2 pg m -3, γ-HCH (lindane) 5.1 pg m -3, endosulfan 4.8 pg m -3 and dieldrin 1.9 pg m -3. Concentrations of Σ-chlordanes, DDEs and heptachlor epoxide were generally similar and lower than those of α-HCH and γ-HCH. The concentrations of most chlorinated pesticides did not show any clear seasonal variation, with the exception of γ-HCH, which had maximum concentration in August in both years. The average annual mean for ΣPBDEs was 1.14 ± 0.81 pg m -3. The predominant congeners measured in Nuuk were BDE-47 and BDE-99 followed by BDE-100, -153 and -28, indicating the use of penta-BDE technical products as the main source. A clear seasonal variation of PBDE concentrations was observed with maximum concentrations occurring in the summer months. The ΣPCNs concentrations ranged between 0.062 and 0.258 pg m -3 with an annual mean concentration of 0.161 ± 0.004 pg m -3. The PCNs profile was dominated by the tetra-PCNs (74% of the annual mean) and the penta-PCNs (18% of the annual mean). A seasonal trend for ΣPCNs was not observed. Atmospheric concentrations of the investigated compounds were correlated with temperature and anthropogenic CO in order to obtain information about their transport pattern. Positive correlations were found between CO and chlordanes, p, p'-DDE and trifluralin, while a negative correlation was found for γ-HCH. A significant correlation with temperature variations was found for dieldrin, heptachlor epoxide, α-HCH, γ-HCH, BDE-47, BDE-99 and tetra-PCNs, which indicates that re-emission of these compounds from previously contaminated surfaces as an important factor for the observed variations in concentrations.

  17. Atmospheric concentrations of organochlorine pesticides, polybrominated diphenyl ethers and polychloronaphthalenes in Nuuk, South-West Greenland

    DEFF Research Database (Denmark)

    Bossi, Rossana; Skov, Henrik; Vorkamp, Katrin

    2008-01-01

    Atmospheric concentrations of organochlorine pesticides (OCs), polybrominated diphenyl ethers (PBDEs) and polychloronaphthalenes (PCNs) were measured for the first time in Nuuk, Greenland in 2004 and 2005. The annual mean concentrations af the measured OCs were: α-HCH 20.2 pg m-3, Υ-HCH (lindane) 5......-HCH, which had maximum concentration in August in both years. The average annual mean for ΣPBDEs was 1.14 ± 0.81 pg m-3. The predominant congeners measured in Nuuk were BDE-47 and BDE-99 followed by BDE-100, -153 and -28, indicating the use of penta-BDE technical products as the main source. A clear seasonal...

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

    Science.gov (United States)

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

    1984-01-01

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

  19. Study on the surface oxidation resistance of uranium metal in the atmosphere of carbon monoxide

    International Nuclear Information System (INIS)

    Wang Xiaolin; Fu Yibei; Xie Renshou

    1999-01-01

    The surface reactions of different layers on uranium metal with carbon monoxide at 25, 80 and 200 degree C are studied by X-ray photoelectron spectroscopy (XPS). The experimental results show that the carbon monoxide is adsorbed on the surface oxide layer of uranium and interacted each other. The content of oxygen in the surface oxide and O/U ratio are decreased with increasing the exposure of carbon monoxide to the surface layer. The effect of reduction on the metal surface is more obviously with a higher temperature and increasing of layer thickness. The investigation indicates the uranium metal has resistance to further oxidation in the atmosphere of carbon monoxide

  20. Potential ocean–atmosphere preconditioning of late autumn Barents-Kara sea ice concentration anomaly

    Directory of Open Access Journals (Sweden)

    Martin P. King

    2016-02-01

    Full Text Available Many recent studies have revealed the importance of the climatic state in November on the seasonal climate of the subsequent winter. In particular, it has been shown that interannual variability of sea ice concentration (SIC over the Barents-Kara (BK seas in November is linked to winter atmospheric circulation anomaly that projects on the North Atlantic Oscillation. Understanding the lead–lag processes involving the different components of the climate system from autumn to winter is therefore important. This note presents dynamical interpretation for the ice-ocean–atmosphere relationships that can affect the BK SIC anomaly in late autumn. It is found that cyclonic (anticyclonic wind anomaly over the Arctic in October, by Ekman drift, can be responsible for positive (negative SIC in the BK seas in November. The results also suggest that ocean heat transport via the Barents Sea Opening in September and October can contribute to BK SIC anomaly in November.

  1. Factors controlling temporal variability of near-ground atmospheric 222Rn concentration over central Europe

    Science.gov (United States)

    Zimnoch, M.; Wach, P.; Chmura, L.; Gorczyca, Z.; Rozanski, K.; Godlowska, J.; Mazur, J.; Kozak, K.; Jeričević, A.

    2014-09-01

    Concentration of radon (222Rn) in the near-ground atmosphere has been measured quasi-continuously from January 2005 to December 2009 at two continental sites in Europe: Heidelberg (south-west Germany) and Krakow (southern Poland). The atmosphere was sampled at ca. 30 and 20 m above the local ground. Both stations were equipped with identical instruments. Regular observations of 222Rn were supplemented by measurements of surface fluxes of this gas in the Krakow urban area, using two different approaches. The measured concentrations of 222Rn varied at both sites in a wide range, from less than 2.0 Bq m-3 to approximately 40 Bq m-3 in Krakow and 35 Bq m-3 in Heidelberg. The mean 222Rn content in Krakow, when averaged over the entire observation period, was 30% higher than in Heidelberg (5.86 ± 0.09 and 4.50 ± 0.07 Bq m-3, respectively). Distinct seasonality of 222Rn signal is visible in the obtained time series of 222Rn concentration, with higher values recorded generally during late summer and autumn. The surface 222Rn fluxes measured in Krakow also revealed a distinct seasonality, with broad maximum observed during summer and early autumn and minimum during the winter. When averaged over a 5-year observation period, the night-time surface 222Rn flux was equal to 46.8 ± 2.4 Bq m-2 h-1. Although the atmospheric 222Rn levels at Heidelberg and Krakow appeared to be controlled primarily by local factors, it was possible to evaluate the "continental effect" in atmospheric 222Rn content between both sites, related to gradual build-up of 222Rn concentration in the air masses travelling between Heidelberg and Krakow. The mean value of this build-up was equal to 0.78 ± 0.12 Bq m-3. The measured minimum 222Rn concentrations at both sites and the difference between them was interpreted in the framework of a simple box model coupled with HYSPLIT (Hybrid Single Particle Lagrangian Integrated Trajectory) analysis of air mass trajectories. The best fit of experimental data was

  2. Catalytic Oxidation of Benzophenone Hydrazone with Alumina-supported KMnO4 under Oxygen Atmosphere

    International Nuclear Information System (INIS)

    Lee, Kang Hyeok; Ko, Kwang Youn

    2006-01-01

    KMnO 4 /alumina reagent, which is cheap and environmentally safe, can serve as a catalytic oxidant under O 2 atmosphere for the oxidation of benzophenone hydrazone. To the best of our knowledge, the present works are the first example where KMnO 4 /alumina reagent acts as a catalytic oxidant under O 2 atmosphere. Diphenyldiazomethane (Ph 2 CN 2 ) is widely used for the protection of carboxylic acids by conversion to their diphenylmethyl (dpm) esters since dpm group can be easily deprotected by mild acidic condition or hydrogenolysis, especially in the field of b-lactams and peptides. Diphenyldiazomethane has been prepared by the oxidation of benzophenone hydrazone with reagents such as active manganese dioxide, mercuric oxide, peracetic acid, iodosobenzene diacetate or OXONE. However, some methods suffer from a disadvantage such as toxic nature of reagent, strong oxidative conditions or incompatibility with certain functional groups. For example, OXONE may not be employed for the in situ protection of carboxylic acid containing sulfide group due to the possibility of the concomitant oxidation of sulfide group

  3. Atmospheric nitrogen deposition influences denitrification and nitrous oxide production in lakes.

    Science.gov (United States)

    McCrackin, Michelle L; Elser, James J

    2010-02-01

    Microbially mediated denitrification is an important process that may ameliorate the effects of nitrogen (N) loading by permanently removing excess N inputs. In this study, we measured the rate of denitrification and nitrous oxide (N2O) production during denitrification in sediments from 32 Norwegian lakes at the high and low ends of a gradient of atmospheric N deposition. Denitrification and N2O production rates averaged 41.7 and 1.1 micromol N x m(-2) x h(-1), respectively, for high-deposition lakes. There was no detectable denitrification or N2O production in low-deposition lakes. Epilimnetic nitrate concentration was strongly correlated with denitrification rate (r2 = 0.67). We also measured the denitrification rate in response to experimental additions of organic carbon, nitrate, and phosphorus. Experimental nitrate additions stimulated denitrification in sediments of all lakes, regardless of N deposition level. In fact, the rate of denitrification in nitrate-amended treatments was the same magnitude for lakes in both deposition areas. These findings suggest that lake sediments possess considerable capacity to remove nitrate and that this capacity has not been saturated under conditions of chronic N loading. Further, nitrous oxide was nearly 3% of the total gaseous product during denitrification in high-deposition lakes, a fraction that is comparable to polluted marine sediments. Our findings suggest that, while lakes play an important role in N removal in the landscape, they may be a source of N2O emissions, especially in areas subject to elevated N inputs.

  4. Thermal stability of pulsed laser deposited iridium oxide thin films at low oxygen atmosphere

    Science.gov (United States)

    Gong, Yansheng; Wang, Chuanbin; Shen, Qiang; Zhang, Lianmeng

    2013-11-01

    Iridium oxide (IrO2) thin films have been regarded as a leading candidate for bottom electrode and diffusion barrier of ferroelectric capacitors, some process related issues need to be considered before integrating ferroelectric capacitors into memory cells. This paper presents the thermal stability of pulsed laser deposited IrO2 thin films at low oxygen atmosphere. Emphasis was given on the effect of post-deposition annealing temperature at different oxygen pressure (PO2) on the crystal structure, surface morphology, electrical resistivity, carrier concentration and mobility of IrO2 thin films. The results showed that the thermal stability of IrO2 thin films was strongly dependent on the oxygen pressure and annealing temperature. IrO2 thin films can stably exist below 923 K at PO2 = 1 Pa, which had a higher stability than the previous reported results. The surface morphology of IrO2 thin films depended on PO2 and annealing temperature, showing a flat and uniform surface for the annealed films. Electrical properties were found to be sensitive to both the annealing temperature and oxygen pressure. The room-temperature resistivity of IrO2 thin films with a value of 49-58 μΩ cm increased with annealing temperature at PO2 = 1 Pa. The thermal stability of IrO2 thin films as a function of oxygen pressure and annealing temperature was almost consistent with thermodynamic calculation.

  5. Optimizing the electrical excitation of an atmospheric pressure plasma advanced oxidation process.

    Science.gov (United States)

    Olszewski, P; Li, J F; Liu, D X; Walsh, J L

    2014-08-30

    The impact of pulse-modulated generation of atmospheric pressure plasma on the efficiency of organic dye degradation has been investigated. Aqueous samples of methyl orange were exposed to low temperature air plasma and the degradation efficiency was determined by absorbance spectroscopy. The plasma was driven at a constant frequency of 35kHz with a duty cycle of 25%, 50%, 75% and 100%. Relative concentrations of dissolved nitrogen oxides, pH, conductivity and the time evolution of gas phase ozone were measured to identify key parameters responsible for the changes observed in degradation efficiency. The results indicate that pulse modulation significantly improved dye degradation efficiency, with a plasma pulsed at 25% duty showing a two-fold enhancement. Additionally, pulse modulation led to a reduction in the amount of nitrate contamination added to the solution by the plasma. The results clearly demonstrate that optimization of the electrical excitation of the plasma can enhance both degradation efficiency and the final water quality. Copyright © 2014 Elsevier B.V. All rights reserved.

  6. Atmospheric CO2 Concentration Measurements with Clouds from an Airborne Lidar

    Science.gov (United States)

    Mao, J.; Abshire, J. B.; Kawa, S. R.; Riris, H.; Allan, G. R.; Hasselbrack, W. E.; Numata, K.; Chen, J. R.; Sun, X.; DiGangi, J. P.; Choi, Y.

    2017-12-01

    Globally distributed atmospheric CO2 concentration measurements with high precision, low bias and full seasonal sampling are crucial to advance carbon cycle sciences. However, two thirds of the Earth's surface is typically covered by clouds, and passive remote sensing approaches from space are limited to cloud-free scenes. NASA Goddard is developing a pulsed, integrated-path differential absorption (IPDA) lidar approach to measure atmospheric column CO2 concentrations, XCO2, from space as a candidate for NASA's ASCENDS mission. Measurements of time-resolved laser backscatter profiles from the atmosphere also allow this technique to estimate XCO2 and range to cloud tops in addition to those to the ground with precise knowledge of the photon path-length. We demonstrate this measurement capability using airborne lidar measurements from summer 2017 ASCENDS airborne science campaign in Alaska. We show retrievals of XCO2 to ground and to a variety of cloud tops. We will also demonstrate how the partial column XCO2 to cloud tops and cloud slicing approach help resolving vertical and horizontal gradient of CO2 in cloudy conditions. The XCO2 retrievals from the lidar are validated against in situ measurements and compared to the Goddard Parameterized Chemistry Transport Model (PCTM) simulations. Adding this measurement capability to the future lidar mission for XCO2 will provide full global and seasonal data coverage and some information about vertical structure of CO2. This unique facility is expected to benefit atmospheric transport process studies, carbon data assimilation in models, and global and regional carbon flux estimation.

  7. Non-thermal atmospheric pressure HF plasma source: generation of nitric oxide and ozone for bio-medical applications

    Science.gov (United States)

    Kühn, S.; Bibinov, N.; Gesche, R.; Awakowicz, P.

    2010-01-01

    A new miniature high-frequency (HF) plasma source intended for bio-medical applications is studied using nitrogen/oxygen mixture at atmospheric pressure. This plasma source can be used as an element of a plasma source array for applications in dermatology and surgery. Nitric oxide and ozone which are produced in this plasma source are well-known agents for proliferation of the cells, inhalation therapy for newborn infants, disinfection of wounds and blood ozonation. Using optical emission spectroscopy, microphotography and numerical simulation, the gas temperature in the active plasma region and plasma parameters (electron density and electron distribution function) are determined for varied nitrogen/oxygen flows. The influence of the gas flows on the plasma conditions is studied. Ozone and nitric oxide concentrations in the effluent of the plasma source are measured using absorption spectroscopy and electro-chemical NO-detector at variable gas flows. Correlations between plasma parameters and concentrations of the particles in the effluent of the plasma source are discussed. By varying the gas flows, the HF plasma source can be optimized for nitric oxide or ozone production. Maximum concentrations of 2750 ppm and 400 ppm of NO and O3, correspondingly, are generated.

  8. Degradation of superconducting Nb/NbN films by atmospheric oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Henry, Michael David; Wolfley, Steven L.; Young, Travis Ryan; Monson, Todd; Pearce, Charles Joseph; Lewis, Rupert M.; Clark, Blythe; Brunke, Lyle Brent; Missert, Nancy A.

    2017-03-01

    Niobium and niobium nitride thin films are transitioning from fundamental research toward wafer scale manufacturing with technology drivers that include superconducting circuits and electronics, optical single photon detectors, logic, and memory. Successful microfabrication requires precise control over the properties of sputtered superconducting films, including oxidation. Previous work has demonstrated the mechanism in oxidation of Nb and how film structure could have deleterious effects upon the superconducting properties. This study provides an examination of atmospheric oxidation of NbN films. By examination of the room temperature sheet resistance of NbN bulk oxidation was identified and confirmed by secondary ion mass spectrometry. As a result, Meissner magnetic measurements confirmed the bulk oxidation not observed with simple cryogenic resistivity measurements.

  9. Oxidation of atmospheric molecular tritium in plant leaves, lichens and mosses

    Energy Technology Data Exchange (ETDEWEB)

    Ichimasa, Michiko; Ichimasa, Yusuke; Yagi, Yoshimi; Ko, Rinkei [Ibaraki Univ., Mito (Japan). Faculty of Science; Suzuki, Masatomo; Akita, Yasukazu

    1989-12-01

    The oxidation of atmospheric molecular tritium (HT) in vegetation was determined by in vitro experiments for pine needles, pine bark, lichens attached to pine trees, taken from a coastal pine forest in Ibaraki prefecture and comparison of such measurements was made with those in soil. The oxidation of HT in pine needles was extremely low, being only about 1/40000 that in the surface soil of a pine forest, whereas its oxidation in pine bark with a lichen was almost 1000-7000 times higher than that in pine needles. HT oxidation in pine bark, a lichen and a moss was determined in each case under light and dark conditions and was found to be essentially the same. All mosses and lichens examined in the present study were found to have unusually high levels of HT oxidation whether their habitat was tree or ground surface. (author).

  10. Oxidation of atmospheric molecular tritium in plant leaves, lichens and mosses

    International Nuclear Information System (INIS)

    Ichimasa, Michiko; Ichimasa, Yusuke; Yagi, Yoshimi; Ko, Rinkei; Suzuki, Masatomo; Akita, Yasukazu.

    1989-01-01

    The oxidation of atmospheric molecular tritium (HT) in vegetation was determined by in vitro experiments for pine needles, pine bark, lichens attached to pine trees, taken from a coastal pine forest in Ibaraki prefecture and comparison of such measurements was made with those in soil. The oxidation of HT in pine needles was extremely low, being only about 1/40000 that in the surface soil of a pine forest, whereas its oxidation in pine bark with a lichen was almost 1000-7000 times higher than that in pine needles. HT oxidation in pine bark, a lichen and a moss was determined in each case under light and dark conditions and was found to be essentially the same. All mosses and lichens examined in the present study were found to have unusually high levels of HT oxidation whether their habitat was tree or ground surface. (author)

  11. Microstructure of oxides in thermal barrier coatings grown under dry/humid atmosphere

    International Nuclear Information System (INIS)

    Zhou Zhaohui; Guo Hongbo; Wang Juan; Abbas, Musharaf; Gong Shengkai

    2011-01-01

    Graphical abstract: The presence of water vapor promoted the formation of spinels in the TBC. Highlights: → Thermal barrier coatings are produced by electron beam physical vapour deposition. → Oxidation behaviour of the coatings at 1100 deg. C has been investigated in dry/humid O 2 . → Thermally grown oxides formed in the coatings are characterized. → The presence of water vapour promotes the formation of spinel in the TBCs. - Abstract: The microstructure of thermally grown oxide (TGO) in thermal barrier coatings (TBCs) oxidized under dry/humid atmosphere at 1100 deg. C has been characterized by transmission electron microscopy. A thin and continuous oxide layer is formed in the as-deposited TBCs produced by electron beam physical vapor deposition. The TGO formed in dry atmosphere consists of an outer layer of fine α-alumina, zirconia grains and an inner layer of columnar α-alumina grains. However, a small amount of spinel is observed in the TGO under humid atmosphere. The presence of water vapour promotes the formation of spinel.

  12. Carbon oxidation state as a metric for describing the chemistry of atmospheric organic aerosol

    Energy Technology Data Exchange (ETDEWEB)

    Massachusetts Institute of Technology; Kroll, Jesse H.; Donahue, Neil M.; Jimenez, Jose L.; Kessler, Sean H.; Canagaratna, Manjula R.; Wilson, Kevin R.; Altieri, Katye E.; Mazzoleni, Lynn R.; Wozniak, Andrew S.; Bluhm, Hendrik; Mysak, Erin R.; Smith, Jared D.; Kolb, Charles E.; Worsnop, Douglas R.

    2010-11-05

    A detailed understanding of the sources, transformations, and fates of organic species in the environment is crucial because of the central roles that organics play in human health, biogeochemical cycles, and Earth's climate. However, such an understanding is hindered by the immense chemical complexity of environmental mixtures of organics; for example, atmospheric organic aerosol consists of at least thousands of individual compounds, all of which likely evolve chemically over their atmospheric lifetimes. Here we demonstrate the utility of describing organic aerosol (and other complex organic mixtures) in terms of average carbon oxidation state (OSC), a quantity that always increases with oxidation, and is readily measured using state-of-the-art analytical techniques. Field and laboratory measurements of OSC , using several such techniques, constrain the chemical properties of the organics and demonstrate that the formation and evolution of organic aerosol involves simultaneous changes to both carbon oxidation state and carbon number (nC).

  13. Atmospheric plasma generates oxygen atoms as oxidizing species in aqueous solutions

    International Nuclear Information System (INIS)

    Hefny, Mohamed Mokhtar; Pattyn, Cedric; Benedikt, Jan; Lukes, Petr

    2016-01-01

    A remote microscale atmospheric pressure plasma jet ( µ APPJ) with He, He/H 2 O, He/O 2 , and He/O 2 /H 2 O gas mixtures was used to study the transport of reactive species from the gas phase into the liquid and the following aqueous phase chemistry. The effects induced by the µ APPJ in water were quantitatively studied using phenol as a chemical probe and by measuring H 2 O 2 concentration and pH values. These results were combined with the analysis of the absolute densities of the reactive species and the modeling of convective/diffusion transport and recombination reactions in the effluent of the plasma jet. Additionally, modified plasma jets were used to show that the role of emitted photons in aqueous chemistry is negligible for these plasma sources. The fastest phenol degradation was measured for the He/O 2 plasma, followed by He/H 2 O, He/O 2 /H 2 O, and He plasmas. The modeled quantitative flux of O atoms into the liquid in the He/O 2 plasma case was highly comparable with the phenol degradation rate and showed a very high transfer efficiency of reactive species from the plasma into the liquid, where more than half of the O atoms leaving the jet nozzle entered the liquid. The results indicate that the high oxidative effect of He/O 2 plasma was primarily due to solvated O atoms, whereas OH radicals dominated the oxidative effects induced in water by plasmas with other gas mixtures. These findings help to understand, in a quantitative way, the complex interaction of cold atmospheric plasmas with aqueous solutions and will allow a better understanding of the interaction of these plasmas with water or buffered solutions containing biological macromolecules, microorganisms, or even eukaryotic cells. Additionally, the µ APPJ He/O 2 plasma source seems to be an ideal tool for the generation of O atoms in aqueous solutions for any future studies of their reactivity. (paper)

  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. Atmospheric CO{sub 2}, trace gas and CN concentrations in Vaerrioe

    Energy Technology Data Exchange (ETDEWEB)

    Ahonen, T; Aalto, P; Kulmala, M; Rannik, U; Vesala, T [Helsinki Univ. (Finland). Dept. of Physics; Hari, P; Pohja, T [Helsinki Univ. (Finland). Dept. of Forest Ecology

    1996-12-31

    The Vaerrioe environmental measurement station is founded in 1991. The aim of the station is to obtain more information on air quality influenced by Kola industrial areas and effects of pollutants on photosynthesis in subarctic climate. In the station air quality and meteorological quantities are measured together with photosynthesis, which makes it quite unique in comparison with other measurement stations located in northern Finland. The measurements also provide information of aerosol and trace gas concentrations in order to study the direct and indirect aerosol effects on climate. These measurements also increase the knowledge of atmospheric chemistry and deposition in subarctic conditions

  16. Concentration and isotope composition of atmospheric methane in Walbrzych Coal District

    International Nuclear Information System (INIS)

    Korus, A.; Necki, J.; Kotarba, M.

    2002-01-01

    The closure of hard coal mines in the Walbrzych Coal District led to the reconstruction of carboniferous groundwater horizon and migration of carbon dioxide and methane upward to the surface. Migration of methane is facilitated by systems of fractures, faults and by dense network of shafts, which still remain in connection with the surface. Measurement of the isotopic composition (δ 13 CH 4 ) of methane together with its concentration in atmosphere, yield useful information on the contribution of anthropogenic sources to regional budget of methane. A two component-mixing model was applied to distinguish anthropogenic source. The result of the study, current parameters of anthropogenic source are presented. (author)

  17. Northern European trees show a progressively diminishing response to increasing atmospheric carbon dioxide concentrations

    CSIR Research Space (South Africa)

    Waterhouse, JS

    2004-04-01

    Full Text Available Reviews 23 (2004) 803?810 Northern European trees show a progressively diminishing response to increasing atmospheric carbon dioxide concentrations J.S. Waterhousea,*, V.R. Switsura,b, A.C. Barkera, A.H.C. Cartera,b,{, D.L. Hemmingc, N.J. Loaderd, I..., V.R., Waterhouse, J.S., Heaton, T.H.E., Carter, A.H.C., 1998. Climatic variation andthe stable carbon isotope composition of tree ring cellulose: an intercomparison of Quercus robur, Fagus sylvatica and Pinus silvestris. Tellus 50B, 25?33. J.ggi, M...

  18. CONCENTRATION OF HARMFUL SUBSTANCES REDUCING IN SURFACE LAYER OF ATMOSPHERE AT RHEOSTAT LOCOMOTIVE TESTS

    Directory of Open Access Journals (Sweden)

    E. A. Bondar

    2010-06-01

    Full Text Available It is shown that at present an acceptable way of reducing the concentration of harmful substances in the surface layer of the atmosphere at rheostat tests of locomotives is their dispersion in a large volume of air. Channels, installed above an exhaust pipe of diesel locomotive with a break at the gas flow, work as ejectors. We have solved jointly the equation of aerodynamic characteristics of the ejector device and the equation of diffusion of gases; as a result the calculated dependence for determining the necessary height of ejector device has been obtained.

  19. Atmospheric CO{sub 2}, trace gas and CN concentrations in Vaerrioe

    Energy Technology Data Exchange (ETDEWEB)

    Ahonen, T.; Aalto, P.; Kulmala, M.; Rannik, U.; Vesala, T. [Helsinki Univ. (Finland). Dept. of Physics; Hari, P.; Pohja, T. [Helsinki Univ. (Finland). Dept. of Forest Ecology

    1995-12-31

    The Vaerrioe environmental measurement station is founded in 1991. The aim of the station is to obtain more information on air quality influenced by Kola industrial areas and effects of pollutants on photosynthesis in subarctic climate. In the station air quality and meteorological quantities are measured together with photosynthesis, which makes it quite unique in comparison with other measurement stations located in northern Finland. The measurements also provide information of aerosol and trace gas concentrations in order to study the direct and indirect aerosol effects on climate. These measurements also increase the knowledge of atmospheric chemistry and deposition in subarctic conditions

  20. Measurement and modeling of ozone and nitrogen oxides produced by laser breakdown in oxygen-nitrogen atmospheres.

    Science.gov (United States)

    Gornushkin, Igor B; Stevenson, Chris L; Galbács, Gábor; Smith, Ben W; Winefordner, James D

    2003-11-01

    The production of ozone nad nitrogen oxides was studied during multiple laser breakdown in oxygen-nitrogen mixtures at atmospheric pressure. About 2000 laser shots at 10(10) W cm-2 were delivered into a sealed reaction chamber. The chamber with a long capillary was designed to measure absorption of O3, NO, and NO2 as a function of the number of laser shots. The light source for absorption measurements was the continuum radiation emitted by the plasma during the first 0.2 microsecond of its evolution. A kinetic model was developed that encompassed the principal chemical reactions between the major atmospheric components and the products of laser breakdown. In the model, the laser plasma was treated as a source of nitric oxide and atomic oxygen, whose rates of production were calculated using measured absorption by NO, NO2, and O3. The calculated concentration profiles for NO, NO2, and O3 were in good agreement with measured profiles over a time scale of 0-200 s. The steady-state concentration of ozone was measured in a flow cell in air. For a single breakdown in air, the estimated steady-state yield of ozone was 2 x 10(12) molecules, which agreed with the model prediction. This study can be of importance for general understanding of laser plasma chemistry and for elucidating the nature of spectral interferences and matrix effects that may take place in applied spectrochemical analysis.

  1. Nitrous oxide and nitrate concentration in under-drainage from arable fields subject to diffuse pollution mitigation measures

    Science.gov (United States)

    Hama-Aziz, Zanist; Hiscock, Kevin; Adams, Christopher; Reid, Brian

    2016-04-01

    Atmospheric nitrous oxide concentrations are increasing by 0.3% annually and a major source of this greenhouse gas is agriculture. Indirect emissions of nitrous oxide (e.g. from groundwater and surface water) account for about quarter of total nitrous oxide emissions. However, these indirect emissions are subject to uncertainty, mainly due to the range in reported emission factors. It's hypothesised in this study that cover cropping and implementing reduced (direct drill) cultivation in intensive arable systems will reduce dissolved nitrate concentration and subsequently indirect nitrous oxide emissions. To test the hypothesis, seven fields with a total area of 102 ha in the Wensum catchment in eastern England have been chosen for experimentation together with two fields (41 ha) under conventional cultivation (deep inversion ploughing) for comparison. Water samples from field under-drainage have been collected for nitrate and nitrous oxide measurement on a weekly basis from April 2013 for two years from both cultivation areas. A purge and trap preparation line connected to a Shimadzu GC-8A gas chromatograph fitted with an electron capture detector was used for dissolved nitrous oxide analysis. Results revealed that with an oilseed radish cover crop present, the mean concentration of nitrate, which is the predominant form of N, was significantly depleted from 13.9 mg N L-1 to 2.5 mg N L-1. However, slightly higher mean nitrous oxide concentrations under the cover crop of 2.61 μg N L-1 compared to bare fields of 2.23 μg N L-1 were observed. Different inversion intensity of soil tended to have no effect on nitrous oxide and nitrate concentrations. The predominant production mechanism for nitrous oxide was nitrification process and the significant reduction of nitrate was due to plant uptake rather than denitrification. It is concluded that although cover cropping might cause a slight increase of indirect nitrous oxide emission, it can be a highly effective

  2. The impact of water concentration on the catalytic oxidation of ethanol on platinum electrode in concentrated phosphoric acid

    Energy Technology Data Exchange (ETDEWEB)

    Camargo, A.P.M.; Previdello, B.A.F.; Varela, H.; Gonzalez, E.R. [Instituto de Quimica de Sao Carlos, Universidade de Sao Paulo, C.P. 780, CEP 13560-970 Sao Carlos, SP (Brazil)

    2010-01-15

    The electro-oxidation of ethanol on platinum in phosphoric acid opens the door to promote the oxidation reaction at higher temperatures. However, the effect of the presence of water is not well understood. In this work, the electro-oxidation of ethanol on platinum was studied in concentrated phosphoric acid containing different concentrations of water at room temperature. The results show that effect of bulk water on the rate electro-oxidation is highest at 0.60 V and decreases for increasing potentials. This was suggested as due to the increasing formation of oxygenated species on the electrode surface with potential, which in turn is more efficient than the increase of water content in the electrolyte. Altogether, these results were interpreted as an evidence of a Langmuir-Hinshelwood step involving oxygenated species as one of the adsorbed partners. (author)

  3. Atmospheric concentrations of 7Be, 10Be and 210Pb in northeast Asia

    International Nuclear Information System (INIS)

    Yamagata, T.; Tada, W.; T saito; Nagai, H.; Murayama, M.; Momoshima, N.; Matsuzaki, H.

    2005-01-01

    Cosmogenic nuclides 7 Be (T 1/2 = 53.3 d) and 10 Be (T 1/2 = 1.5 X 10 6 y) are very useful tracer for the aerosols originated in the upper atmosphere, In the case of 10 Be in surface air, however, two components from upper troposphere and from re-suspended dust from soil are mixed. We try to divide these sources, in order to know an interpretation of aerosol drives. To try to separate the two different source of 10 Be, we use 210 Pb (T 1/2 = 22.3y), progeny of 222 Rn, as continental component. In this study, the distribution of these nuclides in aerosols collected in the Northwest pacific and adjacent seas by employing the research Vessels as cut off the re-suspended dusts from soil are reported. Since research expeditions are mostly short term, continuous observation is very difficult. So we observed at Tokyo and Hachijo-Island, remote island located 300 km south from Tokyo, in 2002-2004. Seasonal variations for 7 Be, 10 Be and 210 Pb concentration were similar pattern at Tokyo and Hachijo-Island. The concentrations were high in April and October to November and low in July to August. Although 210 Pb concentration showed the seasonal variation similar to 7 Be concentration, the average 210 Pb concentration of Tokyo showed the value high about 35% as compared with Hachijo-Island, while the average 7 Be concentration having been mostly in agreement at both points. For the distribution of these nuclide, 7 Be and 10 Be concentrations in ocean air showed strong latitude dependence but 210 Pb concentration depend on distance from continent.

  4. Dose-response and concentration-response relation of rocuronium infusion during propofol nitrous oxide and isoflurane nitrous oxide anaesthesia

    NARCIS (Netherlands)

    Kansanaho, M; Olkkola, KT; Wierda, JMKH

    The dose-response and concentration-response relation of rocuronium infusion was studied in 20 adult surgical patients during proporfol-nitrous oxide and isoflurane (1 MAC) -nitrous oxide anaesthesia. Neuromuscular block was kept constant, initially at 90% and then at 50% with a closed-loop feedback

  5. Effects of oxygen concentration on atmospheric pressure dielectric barrier discharge in Argon-Oxygen Mixture

    Science.gov (United States)

    Li, Xuechun; Li, Dian; Wang, Younian

    2016-09-01

    A dielectric barrier discharge (DBD) can generate a low-temperature plasma easily at atmospheric pressure and has been investigated for applications in trials in cancer therapy, sterilization, air pollution control, etc. It has been confirmed that reactive oxygen species (ROS) play a key role in the processes. In this work, we use a fluid model to simulate the plasma characteristics for DBD in argon-oxygen mixture. The effects of oxygen concentration on the plasma characteristics have been discussed. The evolution mechanism of ROS has been systematically analyzed. It was found that the ground state oxygen atoms and oxygen molecular ions are the dominated oxygen species under the considered oxygen concentrations. With the oxygen concentration increasing, the densities of electrons, argon atomic ions, resonance state argon atoms, metastable state argon atoms and excited state argon atoms all show a trend of decline. The oxygen molecular ions density is high and little influenced by the oxygen concentration. Ground state oxygen atoms density tends to increase before falling. The ozone density increases significantly. Increasing the oxygen concentration, the discharge mode begins to change gradually from the glow discharge mode to Townsend discharge mode. Project supported by the National Natural Science Foundation of China (Grant No. 11175034).

  6. Variation of atmospheric tritium concentration in three chemical forms at Toki, Japan: 2004-12.

    Science.gov (United States)

    Tanaka, M; Uda, T

    2015-11-01

    Atmospheric tritium concentrations of HTO, HT and CH3T have been measured at Toki, Japan, for the environmental impact assessment of tritium for a fusion test facility. According to the data from 2004 to 2012, the concentrations of HT and HTO in water vapour tend to increase in spring. The seasonal variation in HT concentration at Toki was compared with the H2 concentration between 1990 and 2005 at Tae-ahn Peninsula, Republic of Korea, which is at approximately the same latitude as Toki. The monthly average of HT-specific activity varied from 1.24 × 10(5) to 1.76 × 10(5) TU. The peak of the monthly average H2 concentration did not match that of HT. This indicates that the mechanism of the production or the source of HT might be different from the production mechanism of H2. © The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

  7. Manganese oxide phases and morphologies: A study on calcination temperature and atmospheric dependence

    Directory of Open Access Journals (Sweden)

    Matthias Augustin

    2015-01-01

    Full Text Available Manganese oxides are one of the most important groups of materials in energy storage science. In order to fully leverage their application potential, precise control of their properties such as particle size, surface area and Mnx+ oxidation state is required. Here, Mn3O4 and Mn5O8 nanoparticles as well as mesoporous α-Mn2O3 particles were synthesized by calcination of Mn(II glycolate nanoparticles obtained through an economical route based on a polyol synthesis. The preparation of the different manganese oxides via one route facilitates assigning actual structure–property relationships. The oxidation process related to the different MnOx species was observed by in situ X-ray diffraction (XRD measurements showing time- and temperature-dependent phase transformations occurring during oxidation of the Mn(II glycolate precursor to α-Mn2O3 via Mn3O4 and Mn5O8 in O2 atmosphere. Detailed structural and morphological investigations using transmission electron microscopy (TEM and powder XRD revealed the dependence of the lattice constants and particle sizes of the MnOx species on the calcination temperature and the presence of an oxidizing or neutral atmosphere. Furthermore, to demonstrate the application potential of the synthesized MnOx species, we studied their catalytic activity for the oxygen reduction reaction in aprotic media. Linear sweep voltammetry revealed the best performance for the mesoporous α-Mn2O3 species.

  8. CARVE Measurements of Atmospheric Methane Concentrations and Emissions in Arctic and Boreal Alaska

    Science.gov (United States)

    Miller, C. E.; Miller, J. B.; Chang, R. Y.; Sweeney, C.; Karion, A.; Wofsy, S. C.; Henderson, J.; Eluszkiewicz, J.; Mountain, M.; Oechel, W. C.

    2013-12-01

    The Carbon in Arctic Reservoirs Vulnerability Experiment (CARVE) is a NASA Earth Ventures (EV-1) investigation designed to quantify correlations between atmospheric and surface state variables for the Alaskan terrestrial ecosystems through intensive seasonal aircraft campaigns, ground-based observations, and analysis sustained over a 5-year mission. CARVE bridges critical gaps in our knowledge and understanding of Arctic ecosystems, linkages between the Arctic hydrologic and terrestrial carbon cycles, and the feedbacks from fires and thawing permafrost. We present CARVE airborne measurements of spatial and temporal patterns in atmospheric CH4 concentrations and estimated surface-atmosphere emissions for Arctic and Boreal Alaska. Continuous in situ CH4, CO2 and CO data are supplemented by periodic whole air flask samples from which 13CH4 and non-methane hydrocarbons are used to assess the relative contributions of wetlands, fossil fuel combustion, and oil and gas production to the observed CH4 signals. The CARVE project has also initiated monthly 14CH4 sampling at Barrow, AK (BRW) and the CARVE Tower in Fox, AK (CRV) to evaluate seasonal changes in the fraction of old carbon being mobilized via methanogenesis.

  9. Cerium concentrate and mixed rare earth chloride by the oxidative decomposition of bastnaesite in molten sodium hydroxide

    International Nuclear Information System (INIS)

    Iijima, Toshio; Kato, Kazuhiro; Kuno, Toyohiko; Okuwaki, Akitsugu; Umetsu, Yoshiaki; Okabe, Taijiro

    1993-01-01

    Bastnaesite was treated in molten NaOH at 623-777 K for 10-60 min under atmosphere. Cerium-(III) in the ore was easily oxidized 95% or more within 30 min to give an oxidation product composed of solid solutions of CeO 2 -rich and CeO 2 -lean phases and Ce-free rare earth oxide phase. Simultaneously fluoride ion was removed 97% or more. Cerium concentrate was prepared from the oxidation product by leaching with 0.1-3 M HCl solution. The yield of cerium concentrate and the CeO 2 content reached 55-57% and 70-72%, respectively. Mixed rare earth chloride is composed of about 90% rare earth chloride and 10% alkaline earth chloride, and the contents of CeCl 3 , LaCl 3 , NdCl 3 , and PrCl 3 are 11.5, 58.5, 14.4, and 5.4%, respectively. The particle size of resulting cerium concentrate was fairly uniform and about 0.1 μm

  10. Diagnostic of N2(A) concentration in high velocity nitrogen afterglow at atmospheric pressure

    Science.gov (United States)

    Pointu, Anne-Marie; Mintusov, Evgeny

    2009-10-01

    An optical emission diagnostic was used to measure N2(A) concentration in a high velocity (1000 cm/s) N2 flowing afterglow of corona discharge at atmospheric pressure, used for biological decontamination. Introducing impurities of NO (measured at different axial distances and for different values of NO injected flow. Moreover, it has been demonstrated that N2(A) creation comes from N+N+N2 atom recombination with a global rate around 2e-33 cm^6/s, a result which agrees with literature, as well as N2(A) loss mechanisms were confirmed to go via quenching with O and N atoms. The order of magnitude of obtained N2(A) concentration, about 1e11 cm-3, coincides with the results of direct measurement (by Vegard-Kaplan band), using a spectrometer of better resolution.

  11. Atmospheric concentrations of 7Be and 210Pb in Granada, Spain

    International Nuclear Information System (INIS)

    Azahra, M.; Gonzalez-Gomez, C.; Instituto Andaluz de Ciencias de la Tierra, Granada; Lopez-Penalver, J.J.; Camacho-Garcia, M.A.; El Bardouni, T.; Boukhal, H.

    2004-01-01

    Aerosols samples in near-surface air of Granada (Spain) were collected on a weekly basis. The seasonal 210 Pb and 7 Be concentrations were determined during the five-year period, from October 1993 to September 1997. The elements, despite their different origin and their different distribution throughout the atmosphere, present the same seasonal variation. There was a tendency for a maximum during the summer season and a minimum during fall and/or winter. Concentration of 7 Be and 210 Pb and meteorological data have been used in order to determine the periods of the potential radioactive pollution. Deposition of 7 Be occurs primarily by precipitation except during the investigation periods where precipitation was scarce and irregular. (author)

  12. Background concentrations and fluxes of atmospheric ammonia over a deciduous forest

    DEFF Research Database (Denmark)

    Hansen, K.; Pryor, S. C.; Boegh, E.

    2015-01-01

    . In this study, we present two months of half-hourly NH3 fluxes and concentrations measured using a Relaxed Eddy Accumulation system during late summer and fall 2013 above a remote forest site in the central Midwest in USA. Supplementary nitric acid (HNO3) flux and size-resolved aerosol-N measurements are used.......11 μg NH3-N m−2 s−1. The wetness of the forest surfaces (assessed using a proxy of time since precipitation) was found to be crucial in controlling both deposition and emission of atmospheric NH3. Size resolved aerosol concentrations (of NH4+, NO3−, Cl− and SO42−) indicated that the aerosol and gas...

  13. Evaluation of modified atmosphere bag and sulphur dioxide concentrations applied on highbush blueberries fruit (Vaccinium corymbosum L.) cv. Emerald

    OpenAIRE

    Rodríguez, Mario; Wyss, Anddy; Hormazábal, Nelson

    2015-01-01

    Aiming to evaluate techniques for modified atmosphere and application of sulphur anhydride upon parameters of quality of postharvest on blueberry fruit (Vaccinium corymbosum L.) cv. Emerald, an experiment of six treatments was conducted, given by the combination of two factors, modified atmosphere (with and without) and different concentrations of sulphur dioxide (generated by 0, 1 and 2 g of sodium metabisulphite) during 7, 14, 21 and 28 days at 0 °C. The dose of 2 g of modified atmosphere s...

  14. Evidence of precursor phenomena in the Kobe earthquake obtained from atmospheric radon concentration

    Energy Technology Data Exchange (ETDEWEB)

    Yasuoka, Yumi [Kobe Pharmaceutical University, 4-19-1 Mtoyamakitama-machi, Higashinada-ku, Kobe, Hyogo 658-8558 (Japan)]. E-mail: yasuoka@kobepharma-u.ac.jp; Igarashi, George [Science Research Center for Prediction of Earthquakes and Volcanic Eruptions, Tohoku University, 4-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8575 (Japan); Ishikawa, Testuo [National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba 263-8555 (Japan); Tokonami, Shinji [National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba 263-8555 (Japan); Shinogi, Masaki [Kobe Pharmaceutical University, 4-19-1 Mtoyamakitama-machi, Higashinada-ku, Kobe, Hyogo 658-8558 (Japan)

    2006-06-15

    Atmospheric {sup 222}Rn concentrations were determined over a 10a period, which included the date of the Kobe, Japan earthquake, on January 17th 1995. It was found that the seismically related {sup 222}Rn anomaly was higher than the 99% confidence limits for the residual value of atmospheric {sup 222}Rn which had been observed 2 months before. The residual {sup 222}Rn concentration, in which residual values of the daily minimum are the difference between each normal {sup 222}Rn concentration (calculated from January 1984 to December 1993) and the daily minimum {sup 222}Rn concentration (January 1994 to January 1995), was calculated by applying the exponential smoothing method to the residual values for each day. It was found that the fluctuations of the residual values can be fitted very well to a log-periodic oscillation model. The real residual values stopped increasing at 1994.999 (December 31st 1994), which corresponds with the critical point (t {sub c}) of best fit model. This anomalous {sup 222}Rn variation can be seen as the result of local stresses, not primary stresses which directly lead to the Kobe earthquake. On the other hand, when the critical exponent (z) and the radial frequency ({omega}) of the model were simultaneously fixed 0.2 {<=} z {<=} 0.6 and 6 {<=} {omega} {<=} 12, t {sub c} (critical point) was between January 13th 1995 and January 27th 1995. The Kobe earthquake occurrence date (January 17th 1995) is within this range. Therefore this anomalous {sup 222}Rn variation can also be seen as the result of primary stresses which possibly led to the Kobe earthquake. There is a distinct possibility that similar statistical oscillations will be detected in other measurements such as microseismicity, tectonic strain, fluctuation in the ground level, or changes in groundwater elevations and composition.

  15. Surface ozone concentrations in Europe: Links with the regional-scale atmospheric circulation

    Science.gov (United States)

    Davies, T. D.; Kelly, P. M.; Low, P. S.; Pierce, C. E.

    1992-06-01

    Daily surface ozone observations from 1978 (1976 for some analyses) to 1988 for Bottesford (United Kingdom), Cabauw, Kloosterburen (The Netherlands), Hohenpeissenberg, Neuglobsow, Hamburg, and Arkona (Germany) are used to analyze links between surface ozone variations and the atmospheric circulation. A daily Europe-wide synoptic classification highlights marked differences between surface ozone/meteorology relationships in summer and winter. These relationships are characterized by correlations between daily surface ozone concentrations at each station and a local subregional surface pressure gradient (a wind speed index). Although there are geographical variations, which are explicable in terms of regional climatology, there are distinct annual cycles. In summer, the surface ozone/wind speed relationship exhibits the expected negative sign; however, in winter, the relationship is, in the main, strongly positive, especially at those stations which are more influenced by the vigorous westerlies. Spring and autumn exhibit negative, positive, or transitional (between summer and winter) behavior, depending on geographical position. It is suggested that these relationships reflect the importance of vertical exchange from the free troposphere to the surface in the nonsummer months. Composite surface pressure patterns and surface pressure anomaly (from the long-term mean) patterns associated with high surface ozone concentrations on daily and seasonal time scales are consistent with the surface ozone/wind speed relationships. Moreover, they demonstrate that high surface ozone concentrations, in a climatological time frame, can be associated with mean surface pressure patterns which have a synoptic reality and are robust. Such an approach may be useful in interpreting past variations in surface ozone and may help to isolate the effect of human activity. It is also possible that assessments can be made of the effect of projected future changes in the atmospheric circulation

  16. Analyzing nitrogen concentration using carrier illumination (CI) technology for DPN ultra-thin gate oxide

    International Nuclear Information System (INIS)

    Li, W.S.; Wu, Bill; Fan, Aki; Kuo, C.W.; Segovia, M.; Kek, H.A.

    2005-01-01

    Nitrogen concentration in the gate oxide plays a key role for 90 nm and below ULSI technology. Techniques like secondary ionization mass spectroscopy (SIMS) and X-ray photoelectron spectroscopy (XPS) are commonly used for understanding N concentration. This paper describes the application of the carrier illuminationTM (CI) technique to measure the nitrogen concentration in ultra-thin gate oxides. A set of ultra-thin gate oxide wafers with different DPN (decoupled plasma nitridation) treatment conditions were measured using the CI technique. The CI signal has excellent correlation with the N concentration as measured by XPS

  17. Monitoring network of atmospheric Radon-222 concentration in East Asia and backward trajectory analysis of Radon-222 concentration trend at a small solitary island on pacific ocean

    International Nuclear Information System (INIS)

    Ohkura, Takehisa; Yamazawa, Hiromi; Moriizumi, Jun; Hirao, Shigekazu; Iida, Takao; Guo Qiuju; Tohjima, Yasunori

    2009-01-01

    A monitoring network of atmospheric 222 Rn concentration as a tracer for long-range transport in East Asia was established. Atmospheric 222 Rn concentration at Beijing, which is located on China Continent was 10-20 Bq m -3 , at Nagoya, which is located on edge of terrestrial area was 3-10 Bq m -3 and at Hachijo-jima and Hateruma-jima, which are solitary islands in Pacific Ocean was 0.5-3 Bq m -3 , respectively. The atmospheric 222 Rn concentration variations were different from sites. The 222 Rn concentration was the lowest in the summer and the highest in the winter except Nagoya where the highest was observed in the autumn and the lowest in the spring. Diurnal variations were measured at Beijing and Nagoya. In contrast, diurnal variations were not measured but several-day-cycle variations were measured at Hachijo-jima and Hateruma-jima. It was pointed out by this study that the several-day-cycle variations at Hachijo-jima were dependent on synoptic-scale atmospheric disturbance. 222 Rn concentration increased rapidly after a cold front passed through Hachijo-jima. Backward trajectory analysis of the relationship between atmospheric 222 Rn concentrations at Hachijo-jima and transport pathway of air mass indicates that air mass transported from China and Siberia has high concentration 222 Rn and air mass transported from Pacific Ocean has low concentration 222 Rn. In winter, atmospheric 222 Rn concentrations at Hachijo-jima is dependent on vertical transport pathway rather than horizontal transport pathway. (author)

  18. Contributions of Organic Sources to Atmospheric Aerosol Particle Concentrations and Growth

    Science.gov (United States)

    Russell, L. M.

    2017-12-01

    Organic molecules are important contributors to aerosol particle mass and number concentrations through primary emissions as well as secondary growth in the atmosphere. New techniques for measuring organic aerosol components in atmospheric particles have improved measurements of this contribution in the last 20 years, including Scanning Transmission X-ray Microscopy Near Edge X-ray Absorption Fine Structure (STXM-NEXAFS), Fourier Transform Infrared spectroscopy (FTIR), and High-Resolution Aerosol Mass Spectrometry (AMS). STXM-NEXAFS individual aerosol particle composition illustrated the variety of morphology of organic components in marine aerosols, the inherent relationships between organic composition and shape, and the links between atmospheric aerosol composition and particles produced in smog chambers. This type of single particle microscopy has also added to size distribution measurements by providing evidence of how surface-controlled and bulk-controlled processes contribute to the growth of particles in the atmosphere. FTIR analysis of organic functional groups are sufficient to distinguish combustion, marine, and terrestrial organic particle sources and to show that each of those types of sources has a surprisingly similar organic functional group composition over four different oceans and four different continents. Augmenting the limited sampling of these off-line techniques with side-by-side inter-comparisons to online AMS provides complementary composition information and consistent quantitative attribution to sources (despite some clear method differences). Single-particle AMS techniques using light scattering and event trigger modes have now also characterized the types of particles found in urban, marine, and ship emission aerosols. Most recently, by combining with off-line techniques, single particle composition measurements have separated and quantified the contributions of organic, sulfate and salt components from ocean biogenic and sea spray

  19. Historical record of concentrations of atmospheric trace components deduced from a glacier in the Alps

    International Nuclear Information System (INIS)

    Doescher, A.

    1996-07-01

    A 109 m ice core from a high-alpine glacier (Colle Gnifetti, Monte Rosa massif, 4440 m a.s.l., Switzerland) was used to reconstruct the history of atmospheric trace components. Concentrations of the anions chloride, nitrate, sulfate and the cations sodium, ammonium, potassium, magnesium and calcium were measured with 2.5-5.0 cm resolution in the top 70 m of a 109 m long of the ice core. Dating of the ice core was performed using stratigraphic markers such as historically known Saharan dust events, the atomic bomb horizon and volcanic eruptions and supplemented with the 210 Pb nuclear dating. The record covers the time period from about 1755-1981. The concentrations of nitrate and sulfate show an exponential increase from 1930 and 1870 until 1965, respectively. The factors of increase were 2.3±0.3 and 5.8±0.9, respectively. The chloride concentrations remained constant during this period. A good agreement between the concentrations of sulfate, which were corrected for the contribution of seasalt and mineral dust and the European SO 2 -emissions was found for the last 100 years. The concentrations of sodium, potassium, magnesium and calcium did not show a trend. The concentrations of ammonium increased exponentially between 1870 and 1960 by a factor of 2.2±0.4. The different sources of the trace components were identified using correlation analysis. Sodium and chloride originated from seasalt, magnesium and calcium from geologic erosion. For both, the industrial and pre-industrial period, the dominant source of ammonium and nitrate was conversion of the gaseous precursors NH 3 and HNO 3 . Sulfate concentrations in the industrial period originated from the anthropogenically emitted SO 2 , whereas in the pre-industrial period the geologic source dominated. The Colle Gnifetti accumulates mainly summer snow, and therefore, several test drillings were performed to find a new site with higher accumulation rate. (author) figs., 17 tabs., 50 refs

  20. Radiation-use of a forest exposed to elevated concentrations of atmospheric carbon dioxide

    International Nuclear Information System (INIS)

    DeLucia, E. H.; George, K.; Hamilton, J. G.

    2002-01-01

    Radiation-use efficiency of growth (defined as biomass accumulation per unit of absorbed photosynthetically active radiation) of loblobby pine forest plots exposed to ambient or elevated atmospheric carbon dioxide concentration was compared. Biomass accumulation of the dominant loblobby pines was calculated from monthly measurements of tree growth and site-specific allometric measurements. Leaf area index was estimated by optical, allometric and interfall methods, depending on species. Results showed that depending on tree height, elevated carbon dioxide did not alter the above-ground biomass allocation in loblobby pine. Leaf area index estimates by the different methods were found to vary significantly, but elevated carbon dioxide had only a slight effect on leaf area index in the first three years of this study. The 27 per cent increase in radiation-use efficiency of growth in response to carbon dioxide enrichment is believed to have been caused primarily by the stimulation of biomass increment. It was concluded that long-term increases in atmospheric carbon dioxide concentration can increase the radiation-use efficiency of growth in closed canopy forests, but the magnitude and duration of this increase in uncertain. 57 refs., 2 tabs., 3 figs

  1. Crustal tracers in the atmosphere and ocean: Relating their concentrations, fluxes, and ages

    Science.gov (United States)

    Han, Qin

    Crustal tracers are important sources of key limiting nutrients (e.g., iron) in remote ocean regions where they have a large impact on global biogeochemical cycles. However, the atmospheric delivery of bio-available iron to oceans via mineral dust aerosol deposition is poorly constrained. This dissertation aims to improve understanding and model representation of oceanic dust deposition and to provide soluble iron flux maps by testing observations of crustal tracer concentrations and solubilities against predictions from two conceptual solubility models. First, we assemble a database of ocean surface dissolved Al and incorporate Al cycling into the global Biogeochemical Elemental Cycling (BEC) model. The observed Al concentrations show clear basin-scale differences that are useful for constraining dust deposition. The dynamic mixed layer depth and Al residence time in the BEC model significantly improve the simulated dissolved Al field. Some of the remaining model-data discrepancies appear related to the neglect of aerosol size, age, and air mass characteristics in estimating tracer solubility. Next, we develop the Mass-Age Tracking method (MAT) to efficiently and accurately estimate the mass-weighted age of tracers. We apply MAT to four sizes of desert dust aerosol and simulate, for the first time, global distributions of aerosol age in the atmosphere and at deposition. These dust size and age distributions at deposition, together with independent information on air mass acidity, allow us to test two simple yet plausible models for predicting the dissolution of mineral dust iron and aluminum during atmospheric transport. These models represent aerosol solubility as controlled (1) by a diffusive process leaching nutrients from the dust into equilibrium with the liquid water coating or (2) by a process that continually dissolves nutrients in proportion to the particle surface area. The surface-controlled model better captures the spatial pattern of observed

  2. Mechanistic studies on the OH-initiated atmospheric oxidation of selected aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Nehr, Sascha

    2012-07-01

    Benzene, toluene, the xylenes, and the trimethylbenzenes are among the most abundant aromatic trace constituents of the atmosphere mainly originating from anthropogenic sources. The OH-initiated atmospheric photo-oxidation of aromatic hydrocarbons is the predominant removal process resulting in the formation of O{sub 3} and secondary organic aerosol. Therefore, aromatics are important trace constituents regarding air pollution in urban environments. Our understanding of aromatic photo-oxidation processes is far from being complete. This work presents novel approaches for the investigation of OH-initiated atmospheric degradation mechanisms of aromatic hydrocarbons. Firstly, pulsed kinetic studies were performed to investigate the prompt HO{sub 2} formation from OH+ aromatic hydrocarbon reactions under ambient conditions. For these studies, the existing OH reactivity instrument, based on the flash photolysis/laser-induced fluorescence (FP/LIF) technique, was extended to the detection of HO{sub 2} radicals. The experimental design allows for the determination of HO{sub 2} formation yields and kinetics. Results of the pulsed kinetic experiments complement previous product studies and help to reduce uncertainties regarding the primary oxidation steps. Secondly, experiments with aromatic hydrocarbons were performed under atmospheric conditions in the outdoor atmosphere simulation chamber SAPHIR (Simulation of Atmospheric PHotochemistry In a large Reaction chamber) located at Forschungszentrum Juelich. The experiments were aimed at the evaluation of up-to-date aromatic degradation schemes of the Master Chemical Mechanism (MCMv3.2). The unique combination of analytical instruments operated at SAPHIR allows for a detailed investigation of HO{sub x} and NO{sub x} budgets and for the determination of primary phenolic oxidation product yields. MCMv3.2 deficiencies were identified and most likely originate from shortcomings in the mechanistic representation of ring

  3. Molecular understanding of atmospheric particle formation from sulfuric acid and large oxidized organic molecules

    CERN Document Server

    Schobesberger, Siegfried; Bianchi, Federico; Lönn, Gustaf; Ehn, Mikael; Lehtipalo, Katrianne; Dommen, Josef; Ehrhart, Sebastian; Ortega, Ismael K; Franchin, Alessandro; Nieminen, Tuomo; Riccobono, Francesco; Hutterli, Manuel; Duplissy, Jonathan; Almeida, João; Amorim, Antonio; Breitenlechner, Martin; Downard, Andrew J; Dunne, Eimear M; Flagan, Richard C; Kajos, Maija; Keskinen, Helmi; Kirkby, Jasper; Kupc, Agnieszka; Kürten, Andreas; Kurtén, Theo; Laaksonen, Ari; Mathot, Serge; Onnela, Antti; Praplan, Arnaud P; Rondo, Linda; Santos, Filipe D; Schallhart, Simon; Schnitzhofer, Ralf; Sipilä, Mikko; Tomé, António; Tsagkogeorgas, Georgios; Vehkamäki, Hanna; Wimmer, Daniela; Baltensperger, Urs; Carslaw, Kenneth S; Curtius, Joachim; Hansel, Armin; Petäjä, Tuukka; Kulmala, Markku; Donahue, Neil M; Worsnop, Douglas R

    2013-01-01

    Atmospheric aerosols formed by nucleation of vapors affect radiative forcing and therefore climate. However, the underlying mechanisms of nucleation remain unclear, particularly the involvement of organic compounds. Here, we present high-resolution mass spectra of ion clusters observed during new particle formation experiments performed at the Cosmics Leaving Outdoor Droplets chamber at the European Organization for Nuclear Research. The experiments involved sulfuric acid vapor and different stabilizing species, including ammonia and dimethylamine, as well as oxidation products of pinanediol, a surrogate for organic vapors formed from monoterpenes. A striking resemblance is revealed between the mass spectra from the chamber experiments with oxidized organics and ambient data obtained during new particle formation events at the Hyytiälä boreal forest research station. We observe that large oxidized organic compounds, arising from the oxidation of monoterpenes, cluster directly with single sulfuric acid molec...

  4. A revised method to calculate the concentration time integral of atmospheric pollutants

    International Nuclear Information System (INIS)

    Voelz, E.; Schultz, H.

    1980-01-01

    It is possible to calculate the spreading of a plume in the atmosphere under nonstationary and nonhomogeneous conditions by introducing the ''particle-in-cell'' method (PIC). This is a numerical method by which the transport of and the diffusion in the plume is reproduced in such a way, that particles representing the concentration are moved time step-wise in restricted regions (cells) and separately with the advection velocity and the diffusion velocity. This has a systematical advantage over the steady state Gaussian plume model usually used. The fixed-point concentration time integral is calculated directly instead of being substituted by the locally integrated concentration at a constant time as is done in the Gaussian model. In this way inaccuracies due to the above mentioned computational techniques may be avoided for short-time emissions, as may be seen by the fact that both integrals do not lead to the same results. Also the PIC method enables one to consider the height-dependent wind speed and its variations while the Gaussian model can be used only with averaged wind data. The concentration time integral calculated by the PIC method results in higher maximum values in shorter distances to the source. This is an effect often observed in measurements. (author)

  5. Fire feedbacks over geological time and the evolution of atmospheric oxygen concentration

    Science.gov (United States)

    Mills, B.; Belcher, C.; Lenton, T. M.

    2017-12-01

    During the 4.5 billion year history of the Earth, the concentration of oxygen in the atmosphere has risen from trace levels to today's 21%. Yet over the last 400 million years, O2 concentration appears to have remained within a relatively narrow range (around 15% - 30%), despite dramatic changes in the nature of global biogeochemical cycling. This stability has been crucial for continued animal evolution, and is thought to have arisen through feedbacks between oxygen, wildfire and plant productivity: the strong oxygen- dependence of fire initiation and spread means that global photosynthetic primary productivity is suppressed when oxygen levels are high, and enhanced when levels are low. We present biogeochemical modelling of the long term carbon and oxygen cycles, which aims to capture the operation of the wildfire feedback alongside other key processes. We find that wildfire can effectively stabilize long term oxygen concentrations, but that the nature of this feedback has changed as plant evolution has provided different fuels. Specifically, the evolution of early angiosperms during the Cretaceous period provided new understory fuels that more easily facilitated crown and canopy fires. Adding these dynamics to our model produces a more stable system over long timescales, and the model predicts that oxygen concentration has declined towards the present day - a prediction that is supported by other independent estimates.

  6. Carbon assimilation in Eucalyptus urophylla grown under high atmospheric CO2 concentrations: A proteomics perspective.

    Science.gov (United States)

    Santos, Bruna Marques Dos; Balbuena, Tiago Santana

    2017-01-06

    Photosynthetic organisms may be drastically affected by the future climate projections of a considerable increase in CO 2 concentrations. Growth under a high concentration of CO 2 could stimulate carbon assimilation-especially in C3-type plants. We used a proteomics approach to test the hypothesis of an increase in the abundance of the enzymes involved in carbon assimilation in Eucalyptus urophylla plants grown under conditions of high atmospheric CO 2 . Our strategy allowed the profiling of all Calvin-Benson cycle enzymes and associated protein species. Among the 816 isolated proteins, those involved in carbon fixation were found to be the most abundant ones. An increase in the abundance of six key enzymes out of the eleven core enzymes involved in carbon fixation was detected in plants grown at a high CO 2 concentration. Proteome changes were corroborated by the detection of a decrease in the stomatal aperture and in the vascular bundle area in Eucalyptus urophylla plantlets grown in an environment of high atmospheric CO 2 . Our proteomics approach indicates a positive metabolic response regarding carbon fixation in a CO 2 -enriched atmosphere. The slight but significant increase in the abundance of the Calvin enzymes suggests that stomatal closure did not prevent an increase in the carbon assimilation rates. The sample enrichment strategy and data analysis used here enabled the identification of all enzymes and most protein isoforms involved in the Calvin-Benson-Bessham cycle in Eucalyptus urophylla. Upon growth in CO 2 -enriched chambers, Eucalyptus urophylla plantlets responded by reducing the vascular bundle area and stomatal aperture size and by increasing the abundance of six of the eleven core enzymes involved in carbon fixation. Our proteome approach provides an estimate on how a commercially important C3-type plant would respond to an increase in CO 2 concentrations. Additionally, confirmation at the protein level of the predicted genes involved in

  7. Non-asthmatic patients show increased exhaled nitric oxide concentrations

    Directory of Open Access Journals (Sweden)

    Beatriz M. Saraiva-Romanholo

    2009-01-01

    Full Text Available OBJECTIVE: Evaluate whether exhaled nitric oxide may serve as a marker of intraoperative bronchospasm. INTRODUCTION: Intraoperative bronchospasm remains a challenging event during anesthesia. Previous studies in asthmatic patients suggest that exhaled nitric oxide may represent a noninvasive measure of airway inflammation. METHODS: A total of 146,358 anesthesia information forms, which were received during the period from 1999 to 2004, were reviewed. Bronchospasm was registered on 863 forms. From those, three groups were identified: 9 non-asthmatic patients (Bronchospasm group, 12 asthmatics (Asthma group and 10 subjects with no previous airway disease or symptoms (Control group. All subjects were submitted to exhaled nitric oxide measurements (parts/billion, spirometry and the induced sputum test. The data was compared by ANOVA followed by the Tukey test and Kruskal-Wallis followed by Dunn's test. RESULTS: The normal lung function test results for the Bronchospasm group were different from those of the asthma group (p <0.05. The median percentage of eosinophils in induced sputum was higher for the Asthma [2.46 (0.45-6.83] compared with either the Bronchospasm [0.55 (0-1.26] or the Control group [0.0 (0] (p <0.05; exhaled nitric oxide followed a similar pattern for the Asthma [81.55 (57.6-86.85], Bronchospasm [46.2 (42.0 -62.6] and Control group [18.7 (16.0-24.7] (p< 0.05. CONCLUSIONS: Non-asthmatic patients with intraoperative bronchospasm detected during anesthesia and endotracheal intubation showed increased expired nitric oxide.

  8. Lower thermospheric nitric oxide concentrations derived from WINDII observations of the green nightglow continuum at 553.1 nm

    Directory of Open Access Journals (Sweden)

    C. H. A. von Savigny

    1999-11-01

    Full Text Available Vertical profiles of nitric oxide in the altitude range 90 to 105 km are derived from 553 nm nightglow continuum measurements made with the Wind Imaging Interferometer (WINDII on the Upper Atmosphere Research Satellite (UARS. The profiles are derived under the assumption that the continuum emission is due entirely to the NO+O air afterglow reaction. Vertical profiles of the atomic oxygen density, which are required to determine the nitric oxide concentrations, are derived from coordinated WINDII measurements of the atomic oxygen OI 557.7 nm nightglow emission. Data coverage for local solar times ranging from 20 h to 04 h, and latitudes ranging from 42°S to 42°N, is achieved by zonally averaging and binning data obtained on 18 nights during a two-month period extending from mid-November 1992 until mid-January 1993. The derived nitric oxide concentrations are significantly smaller than those obtained from rocket measurements of the airglow continuum but they do compare well with model expectations and nitric oxide densities measured using the resonance fluorescence technique on the Solar Mesosphere Explorer satellite. The near-global coverage of the WINDII observations and the similarities to the nitric oxide global morphology established from other satellite measurements strongly suggests that the NO+O reaction is the major source of the continuum near 553 nm and that there is no compelling reason to invoke additional sources of continuum emission in this immediate spectral region.Key words. Atmospheric composition and structure (airglow and aurora; thermosphere – composition and chemistry; instruments and techniques

  9. Oxygen potential of uranium--plutonium oxide as determined by controlled-atmosphere thermogravimetry

    International Nuclear Information System (INIS)

    Swanson, G.C.

    1975-10-01

    The oxygen-to-metal atom ratio, or O/M, of solid solution uranium-plutonium oxide reactor fuel is a measure of the concentration of crystal defects in the oxide which affect many fuel properties, particularly, fuel oxygen potential. Fabrication of a high-temperature oxygen electrode, employing an electro-active tip of oxygen-deficient solid-state electrolyte, intended to confirm gaseous oxygen potentials is described. Uranium oxide and plutonium oxide O/M reference materials were prepared by in situ oxidation of high purity metals in the thermobalance. A solid solution uranium-plutonium oxide O/M reference material was prepared by alloying the uranium and plutonium metals in a yttrium oxide crucible at 1200 0 C and oxidizing with moist He at 250 0 C. The individual and solid solution oxides were isothermally equilibrated with controlled oxygen potentials between 800 and 1300 0 C and the equilibrated O/M ratios calculated with corrections for impurities and buoyancy effects. Use of a reference oxygen potential of -100 kcal/mol to produce an O/M of 2.000 is confirmed by these results. However, because of the lengthy equilibration times required for all oxides, use of the O/M reference materials rather than a reference oxygen potential is recommended for O/M analysis methods calibrations. (auth)

  10. Temporal variations of atmospheric CO2 concentration in a temperate deciduous forest in central Japan

    International Nuclear Information System (INIS)

    Murayama, Shohei; Saigusa, Nobuko; Yamamoto, Susumu; Kondo, Hiroaki; Eguchi, Yozo; Chan, Douglas

    2003-01-01

    In order to examine the temporal variation of the atmospheric CO 2 concentration in a temperate deciduous forest, and its relationship with meteorological conditions, continuous measurements of CO 2 and meteorological parameters have been made since 1993 on a tower at Takayama in the central part of Japan. In addition to an average secular increase in atmospheric CO 2 of 1.8 ppm/yr, diurnal variation with a maximum during the night-time to early morning and a minimum in the afternoon is observed from late spring to early fall; the diurnal cycle is not so clearly observed in the remaining seasons of the year. A concentration difference between above and below the canopy, and its diurnal variation, can also be seen clearly in summer. Daily mean concentration data show a prominent seasonal cycle. The maximum and the minimum of the seasonal cycle occur in April and from mid August to mid September, respectively. Day-to-day changes in the diurnal cycle of CO 2 are highly dependent on the day-to-day variations in meteorological conditions. However, CO 2 variations on longer time scales (>10 d) appear to be linearly related to changes in respiration. At Takayama, variations in the 10-d standard deviation of daily mean CO 2 data and 10-d averaged respiration show distinct relationships with soil temperature during spring and fall seasons. In spring, respiration has a stronger exponential dependence on soil temperature than in fall. Interestingly, in summer when soil temperature becomes greater than about 15 deg C, biological respiration becomes more variable and independent of the soil temperature. Thus, at the Takayama site, the Q10 relationship is seasonally dependent, and does not represent well the biological respiration process when the soil temperature rises above 15 deg C

  11. Exchange of carbonyl sulfide (OCS) between soils and atmosphere under various CO2 concentrations

    Science.gov (United States)

    Bunk, Rüdiger; Behrendt, Thomas; Yi, Zhigang; Andreae, Meinrat O.; Kesselmeier, Jürgen

    2017-06-01

    A new continuous integrated cavity output spectroscopy analyzer and an automated soil chamber system were used to investigate the exchange processes of carbonyl sulfide (OCS) between soils and the atmosphere under laboratory conditions. The exchange patterns of OCS between soils and the atmosphere were found to be highly dependent on soil moisture and ambient CO2 concentration. With increasing soil moisture, OCS exchange ranged from emission under dry conditions to an uptake within an optimum moisture range, followed again by emission at high soil moisture. Elevated CO2 was found to have a significant impact on the exchange rate and direction as tested with several soils. There is a clear tendency toward a release of OCS at higher CO2 levels (up to 7600 ppm), which are typical for the upper few centimeters within soils. At high soil moisture, the release of OCS increased sharply. Measurements after chloroform vapor application show that there is a biotic component to the observed OCS exchange. Furthermore, soil treatment with the fungi inhibitor nystatin showed that fungi might be the dominant OCS consumers in the soils we examined. We discuss the influence of soil moisture and elevated CO2 on the OCS exchange as a change in the activity of microbial communities. Physical factors such as diffusivity that are governed by soil moisture also play a role. Comparing KM values of the enzymes to projected soil water CO2 concentrations showed that competitive inhibition is unlikely for carbonic anhydrase and PEPCO but might occur for RubisCO at higher CO2 concentrations.

  12. Effects of an oxidizing atmosphere in a spent fuel packaging facility

    International Nuclear Information System (INIS)

    Einziger, R.E.

    1991-09-01

    Sufficient oxidation of spent fuel can cause a cladding breach to propagate, resulting in dispersion of fuel particulates and gaseous radionuclides. The literature for spent fuel oxidation in storage and disposal programs was reviewed to evaluate the effect of an oxidizing atmosphere in a preclosure packaging facility on (1) physical condition of the fuel and (2) operations in the facility. Effects such as cladding breach propagation, cladding oxidation, rod dilation, fuel dispersal, 14 C and 85 Kr release, and crud release were evaluated. The impact of these effects, due to oxidation, upon a spent fuel handling facility is generally predicted to be less than the impact of similar effects due to fuel rod breached during handling in an inert-atmosphere facility. Preliminary temperature limits of 240 degree C and 227 degree C for a 2-week or 4-week handling period and 175 degree C for 2-year lag storage would prevent breach propagation and fuel dispersal. Additional data that are needed to support the assumptions in this analysis or complete the database were identified

  13. Joint Application of Concentrations and Isotopic Signatures to Investigate the Global Atmospheric Carbon Monoxide Budget: Inverse Modeling Approach

    Science.gov (United States)

    Park, K.; Mak, J. E.; Emmons, L. K.

    2008-12-01

    Carbon monoxide is not only an important component for determining the atmospheric oxidizing capacity but also a key trace gas in the atmospheric chemistry of the Earth's background environment. The global CO cycle and its change are closely related to both the change of CO mixing ratio and the change of source strength. Previously, to estimate the global CO budget, most top-down estimation techniques have been applied the concentrations of CO solely. Since CO from certain sources has a unique isotopic signature, its isotopes provide additional information to constrain its sources. Thus, coupling the concentration and isotope fraction information enables to tightly constrain CO flux by its sources and allows better estimations on the global CO budget. MOZART4 (Model for Ozone And Related chemical Tracers), a 3-D global chemical transport model developed at NCAR, MPI for meteorology and NOAA/GFDL and is used to simulate the global CO concentration and its isotopic signature. Also, a tracer version of MOZART4 which tagged for C16O and C18O from each region and each source was developed to see their contributions to the atmosphere efficiently. Based on the nine-year-simulation results we analyze the influences of each source of CO to the isotopic signature and the concentration. Especially, the evaluations are focused on the oxygen isotope of CO (δ18O), which has not been extensively studied yet. To validate the model performance, CO concentrations and isotopic signatures measured from MPI, NIWA and our lab are compared to the modeled results. The MOZART4 reproduced observational data fairly well; especially in mid to high latitude northern hemisphere. Bayesian inversion techniques have been used to estimate the global CO budget with combining observed and modeled CO concentration. However, previous studies show significant differences in their estimations on CO source strengths. Because, in addition to the CO mixing ratio, isotopic signatures are independent tracers

  14. Long-term trend and variability of atmospheric PM10 concentration in the Po Valley

    Science.gov (United States)

    Bigi, A.; Ghermandi, G.

    2014-05-01

    The limits to atmospheric pollutant concentration set by the European Commission provide a challenging target for the municipalities in the Po Valley, because of the characteristic climatic conditions and high population density of this region. In order to assess climatology and trends in the concentration of atmospheric particles in the Po Valley, a data set of PM10 data from 41 sites across the Po Valley have been analysed, including both traffic and background sites (either urban, suburban or rural). Of these 41 sites, 18 with 10 yr or longer record have been analysed for long-term trend in deseasonalized monthly means, in annual quantiles and in monthly frequency distribution. A widespread significant decreasing trend has been observed at most sites, up to a few percent per year, by a generalized least squares and Theil-Sen method. All 41 sites have been tested for significant weekly periodicity by Kruskal-Wallis test for mean anomalies and by Wilcoxon test for weekend effect magnitude. A significant weekly periodicity has been observed for most PM10 series, particularly in summer and ascribed mainly to anthropic particulate emissions. A cluster analysis has been applied in order to highlight stations sharing similar pollution conditions over the reference period. Five clusters have been found, two encompassing the metropolitan areas of Turin and Milan and their respective nearby sites and the other three clusters gathering northeast, northwest and central Po Valley sites respectively. Finally, the observed trends in atmospheric PM10 have been compared to trends in provincial emissions of particulates and PM precursors, and analysed along with data on vehicular fleet age, composition and fuel sales. A significant basin-wide drop in emissions occurred for gaseous pollutants, contrarily to emissions of PM10 and PM2.5, whose drop was low and restricted to a few provinces. It is not clear whether the decrease for only gaseous emissions is sufficient to explain the

  15. The interaction of the flux errors and transport errors in modeled atmospheric carbon dioxide concentrations

    Science.gov (United States)

    Feng, S.; Lauvaux, T.; Butler, M. P.; Keller, K.; Davis, K. J.; Jacobson, A. R.; Schuh, A. E.; Basu, S.; Liu, J.; Baker, D.; Crowell, S.; Zhou, Y.; Williams, C. A.

    2017-12-01

    Regional estimates of biogenic carbon fluxes over North America from top-down atmospheric inversions and terrestrial biogeochemical (or bottom-up) models remain inconsistent at annual and sub-annual time scales. While top-down estimates are impacted by limited atmospheric data, uncertain prior flux estimates and errors in the atmospheric transport models, bottom-up fluxes are affected by uncertain driver data, uncertain model parameters and missing mechanisms across ecosystems. This study quantifies both flux errors and transport errors, and their interaction in the CO2 atmospheric simulation. These errors are assessed by an ensemble approach. The WRF-Chem model is set up with 17 biospheric fluxes from the Multiscale Synthesis and Terrestrial Model Intercomparison Project, CarbonTracker-Near Real Time, and the Simple Biosphere model. The spread of the flux ensemble members represents the flux uncertainty in the modeled CO2 concentrations. For the transport errors, WRF-Chem is run using three physical model configurations with three stochastic perturbations to sample the errors from both the physical parameterizations of the model and the initial conditions. Additionally, the uncertainties from boundary conditions are assessed using four CO2 global inversion models which have assimilated tower and satellite CO2 observations. The error structures are assessed in time and space. The flux ensemble members overall overestimate CO2 concentrations. They also show larger temporal variability than the observations. These results suggest that the flux ensemble is overdispersive. In contrast, the transport ensemble is underdispersive. The averaged spatial distribution of modeled CO2 shows strong positive biogenic signal in the southern US and strong negative signals along the eastern coast of Canada. We hypothesize that the former is caused by the 3-hourly downscaling algorithm from which the nighttime respiration dominates the daytime modeled CO2 signals and that the latter

  16. Oxidation behavior of a Ni-Fe support in SOFC anode atmosphere

    DEFF Research Database (Denmark)

    Xu, Na; Chen, Ming; Han, Minfang

    2018-01-01

    In this work, we investigated the long-term oxidation behavior of a Ni-Fe (1:1 weight ratio) support for solid oxide fuel cell (SOFC) applications. Ni-Fe supports were obtained through tape casting, high temperature sintering and pre-reducing in 97% H2/N2 (9/91)-3% H2O at 750 and 1000 °C, respect...... annealed in the two atmospheres maintained sufficiently high conductivity. The results from the current work demonstrate that the porous Ni-Fe support can be well employed in SOFCs, especially metal-supported SOFCs....

  17. Intercomparison study of atmospheric methane and carbon dioxide concentrations measured at the Ebre River Delta Station

    Science.gov (United States)

    Occhipinti, Paola; Morguí, Josep Anton; Àgueda, Alba; Batet, Oscar; Borràs, Sílvia; Cañas, Lídia; Curcoll, Roger; Grossi, Claudia; Nofuentes, Manel; Vazquez, Eusebi; Rodó, Xavier

    2015-04-01

    In the framework of the ClimaDat project, IC3 has established a network of eight monitoring stations across the Iberian Peninsula and the Canarian Archipelago with the aim of studying climate processes. The monitoring station at the Ebre River Delta (DEC3) is located in the Ebre River Delta Natural Park (40° 44' N; 0° 47' E) and it is characterized by the typical North-Western Mediterranean climate. Since 2013, atmospheric greenhouse gases (GHG) and 222Rn tracer gas together with the meteorological parameters are continuously measured from a 10 m a.g.l. height tower. Atmospheric GHG (CO2, CH4, CO and N2O) concentrations are determined using a Picarro analyzer G2301 (CO2 and CH4) and a modified gas chromatograph (GC) Agilent 6890N (CO2, CH4, CO and N2O). Open data access is available from the www.climadat.es website. Data collected at the DEC3 station are also submitted to the InGOS platform since this station is part of the InGOS European infrastructure project. Researchers from the Laboratory of the Atmosphere and the Oceans (LAO) at IC3 have performed an intercomparison study at the DEC3 site between three different Picarro analyzers (two Picarro G2301 and one Picarro G2301M), a Los Gatos Research (LGR) analyzer and the GC system already installed at the station. The aim of this study is to compare and assess the measuring agreement between the four optical gas analyzers and the GC. In the first part of the experiment, all instruments have been calibrated using NOAA gases as primary standards analyzing five Praxair provided targets to evaluate the precision of the measuring instruments. Max Plank Institute (MPI) gases have been used as secondary standards for the GC whereas Praxair provided tanks are used as secondary standards for the Picarro and the LGR analyzers. In the second part of the experiment, atmospheric GHG were measured from natural atmospheric air taken from a 10 m a.g.l. inlet. Daily cycles of GHG measurements were carried out using different

  18. Correlations between atmospheric aerosol trace element concentrations and red tide at Port Aransas, Texas, on the Gulf of Mexico

    International Nuclear Information System (INIS)

    Biegalski, S.R.; Villareal, T.A.

    2005-01-01

    Neutron activation analysis (NAA) was employed as an analytical technique to measure atmospheric aerosol concentrations of trace metals in Port Aransas, TX on the Gulf of Mexico. The sources of atmospheric aerosols and the seasonal variation of the sources are explored. High atmospheric iron concentrations are then shown to have a possible correlation to the occurrences of red tide in this region. The data shows that this correlation is plausible, but due to the many factors that affect red tide growth a definitive conclusion may not be reached. The period of study for these measurements was September 12, 2000 to January 4, 2002. (author)

  19. Optical remote sensing of properties and concentrations of atmospheric trace constituents

    Science.gov (United States)

    Vladutescu, Daniela Viviana

    The effect of human activities on the global climate may lead to large disturbances of the economic, social and political circumstances in the middle and long term. Understanding the dynamics of the Earth's climate is therefore of high importance and one of the major scientific challenges of our time. The estimation of the contribution of the Earth's climate system components needs observation and continuous monitoring of various atmospheric physical and chemical parameters. Temperature, water vapor and greenhouse gases concentration, aerosol and clouds loads, and atmospheric dynamics are parameters of particular importance in this respect. The quantification of the anthropogenic influence on the dynamics of these above-mentioned parameters is of crucial importance nowadays but still affected by significant uncertainties. In the present context of these huge uncertainties in our understanding of how these different atmospheric compounds contribute to the radiative forcing, a significant part of my research interest is related to the following topics: (1) Development of lidar (Light Detection and Ranging)-based remote sensing techniques for monitoring atmospheric compounds and processes; (2) Aerosols hygroscopic properties and atmospheric modeling; (3) Water vapor mixing ratio and relative humidity estimation in the troposphere; (4) Characterization of the long-range transported aerosols; (5) Ambient gases detection using Fourier Transform Interferometers (FTIR); (6) Design of inexpensive Fabry Perot Interferometer for visible and near infrared for land and ocean surface remote sensing applications. The lidar-based remote sensing measurement techniques for the monitoring of climate change parameters where implemented at the City College of the City University of New York (CCNY/CUNY) LIDAR station and are presented in the second section of the paper. The geographical location of the CCNY lidar station is 40.86N, -73.86W. Among the lidar retrievals one important

  20. A study on the environmental behavior of global air pollutants based on the continuous measurements of atmospheric radon concentrations

    International Nuclear Information System (INIS)

    Iida, Takao; Yamazawa, Hiromi

    2003-01-01

    Radon is a useful natural radioactive tracer of air transportation of atmospheric pollution, since radon is a noble gas and chemically inert. The atmospheric radon concentration is usually measured by a high-sensitivity electrostatic collection method or a two-filter method. The variations of radon concentrations observed over a solitary island and in the upper atmosphere are suitable for comparing with those of air pollutants. Some numerical simulation models were used to study the radon global transport in the atmosphere. In East Asia, atmospheric radon and air pollutants are transported with the air stream from the continent of China to the Northwestern Pacific Ocean. It is necessary to clarify the transport mechanism from both radon observations at various locations and numerical simulation. (author)

  1. Optical measurements of atomic oxygen concentration, temperature and nitric oxide production rate in flames

    Science.gov (United States)

    Myhr, Franklin Henry

    An optical method for measuring nitric oxide (NO) production rates in flames was developed and characterized in a series of steady, one-dimensional, atmospheric-pressure laminar flames of 0.700 Hsb2/0.199 Nsb2/0.101 COsb2 or 0.700 CHsb4/0.300 Nsb2 (by moles) with dry air, with equivalence ratios from 0.79 to 1.27. Oxygen atom concentration, (O), was measured by two-photon laser-induced fluorescence (LIF), temperature was measured by ultraviolet Rayleigh scattering, and nitrogen concentration was calculated from supplied reactant flows; together this information was used to calculate the NO production rate through the thermal (Zel'dovich) mechanism. Measurements by two other techniques were compared with results from the above method. In the first comparison, gas sampling was used to measure axial NO concentration profiles, the slopes of which were multiplied by velocity to obtain total NO production rates. In the second comparison, LIF measurements of hydroxyl radical (OH) were used with equilibrium water concentrations and a partial equilibrium assumption to find (O). Nitric oxide production rates from all three methods agreed reasonably well. Photolytic interference was observed during (O) LIF measurements in all of the flames; this is the major difficulty in applying the optical technique. Photolysis of molecular oxygen in lean flames has been well documented before, but the degree of interference observed in the rich flames suggests that some other molecule is also dissociating; the candidates are OH, CO, COsb2 and Hsb2O. An extrapolative technique for removing the effects of photolysis from (O) LIF measurements worked well in all flames where NO production was significant. Using the optical method to measure NO production rates in turbulent flames will involve a tradeoff among spatial resolution, systematic photolysis error, and random shot noise. With the conventional laser system used in this work, a single pulse with a resolution of 700 mum measured NO

  2. Coarsening of Pd nanoparticles in an oxidizing atmosphere studied by in situ TEM

    DEFF Research Database (Denmark)

    Simonsen, Søren Bredmose; Chorkendorff, Ib; Dahl, Søren

    2016-01-01

    The coarsening of supported palladium nanoparticles in an oxidizing atmosphere was studied in situ by means of transmission electron microscopy (TEM). Specifically, the Pd nanoparticles were dispersed on a planar and amorphous Al2O3 support and were observed during the exposure to 10 mbar technical...... for the Ostwald ripening process indicates that the observed change in the particle size distribution can be accounted for by wetting of the Al2O3 support by the larger Pd nanoparticles....

  3. Performance Testing of a Photocatalytic Oxidation Module for Spacecraft Cabin Atmosphere Revitalization

    Science.gov (United States)

    Perry, Jay L.; Abney, Morgan B.; Frederick, Kenneth R.; Scott, Joseph P.; Kaiser, Mark; Seminara, Gary; Bershitsky, Alex

    2011-01-01

    Photocatalytic oxidation (PCO) is a candidate process technology for use in high volumetric flow rate trace contaminant control applications in sealed environments. The targeted application for PCO as applied to crewed spacecraft life support system architectures is summarized. Technical challenges characteristic of PCO are considered. Performance testing of a breadboard PCO reactor design for mineralizing polar organic compounds in a spacecraft cabin atmosphere is described. Test results are analyzed and compared to results reported in the literature for comparable PCO reactor designs.

  4. Control methods of radon and its progeny concentration in indoor atmosphere

    International Nuclear Information System (INIS)

    Ramachandran, T.V.; Subba Ramu, M.C.

    1990-01-01

    Exposure to radon-222 and its progeny in indoor atmosphere can result in significant inhalation risk to the population particularly to those living in houses with much higher levels of Rn. There are three methods generally used for the control of Rn and its progeny concentration in the indoor environment: (1) restricting the radon entry, (2) reduction of indoor radon concentration by ventilation or by aircleaning and (3) removal of airborne radon progeny by aerosol reduction. Prominent process of radon entry in most of the residence appears to be the pressure driven flow of soil gas through cracks or through other openings in the basements slab or subfloor. Sealing off these openings or ventilation of the slab or subfloor spaces are the methods of reducing the radon entry rate. Indoor radon progeny levels can also be reduced by decreasing the aerosol load in the dwellings. The results of a few experiments carried out to study the reduction in the working level concentration of radon, by decreasing the aerosol load are discussed in this paper. (author). 9 tabs., 8 figs., 37 refs

  5. Evaluation of correlating factors between 238U concentration measured in fine and course atmospheric particles

    International Nuclear Information System (INIS)

    Peixoto, Claudia Marques; Jacomino, Vanusa Maria Feliciano; Barreto, Alberto Avelar; Dias, Vagner Silva; Dias, Fabiana Ferrari

    2009-01-01

    Air quality is ever more important in function of the enormous proportion of human actions that have affected the environment over the last two centuries. Particulate material is one among many pollutants that can cause great risk to human health and the environment. It can be classified as: Total Suspended Particles (TSP), defined simply as particles with less than 50 μm aerodynamic diameter (one group of these particles can be inhaled and may cause health problems, while others may unfavorably affect the population's quality of life, interfering in environmental conditions and impairing normal community activities); and Inhalable Particles (PM 10 ), defined as those particles with less than 10 μm aerodynamic diameter. These particles penetrate the respiratory system and can reach pulmonary alveoli due to their small size, causing serious health damage. The Nuclear Technology Development Center (CDTN) has monitored air quality around its installations since 2000. CDTN's Environmental Monitoring Program (EMP) includes monitoring radioactivity levels contained in atmospheric TSP. In order to optimize its program, CDTN is carrying out a study to estimate the correlation between concentrations of particulate material measured in TSP and those measured in PM 10 , PI 2.5 and PI 1 , as well as determination of activity concentration for each controlled radionuclide in all parts. The objective of this study is to present preliminary results and report 238 U activity concentration results. (author)

  6. Observations of the uptake of carbonyl sulfide (COS by trees under elevated atmospheric carbon dioxide concentrations

    Directory of Open Access Journals (Sweden)

    L. Sandoval-Soto

    2012-08-01

    Full Text Available Global change forces ecosystems to adapt to elevated atmospheric concentrations of carbon dioxide (CO2. We understand that carbonyl sulfide (COS, a trace gas which is involved in building up the stratospheric sulfate aerosol layer, is taken up by vegetation with the same triad of the enzymes which are metabolizing CO2, i.e. ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco, phosphoenolpyruvate carboxylase (PEP-Co and carbonic anhydrase (CA. Therefore, we discuss a physiological/biochemical acclimation of these enzymes affecting the sink strength of vegetation for COS. We investigated the acclimation of two European tree species, Fagus sylvatica and Quercus ilex, grown inside chambers under elevated CO2, and determined the exchange characteristics and the content of CA after a 1–2 yr period of acclimation from 350 ppm to 800 ppm CO2. We demonstrate that a compensation point, by definition, does not exist. Instead, we propose to discuss a point of uptake affinity (PUA. The results indicate that such a PUA, the CA activity and the deposition velocities may change and may cause a decrease of the COS uptake by plant ecosystems, at least as long as the enzyme acclimation to CO2 is not surpassed by an increase of atmospheric COS. As a consequence, the atmospheric COS level may rise causing an increase of the radiative forcing in the troposphere. However, this increase is counterbalanced by the stronger input of this trace gas into the stratosphere causing a stronger energy reflection by the stratospheric sulfur aerosol into space (Brühl et al., 2012. These data are very preliminary but may trigger a discussion on COS uptake acclimation to foster measurements with modern analytical instruments.

  7. THE SENSITIVITY OF THE GREENHOUSE EFFECT TO CHANGES IN THE CONCENTRATION OF GASES IN PLANETARY ATMOSPHERES

    Directory of Open Access Journals (Sweden)

    Smadar Bressler

    2013-12-01

    Full Text Available We present a radiative transfer model for Earth-Like-Planets (ELP. The model allows the assessment of the effect of a change in the concentration of an atmospheric component, especially a greenhouse gas (GHG, on the surface temperature of a planet. The model is based on the separation between the contribution of the short wavelength molecular absorption and the long wavelength one. A unique feature of the model is the condition of energy conservation at every point in the atmosphere. The radiative transfer equation is solved in the two stream approximation without assuming the existence of an LTE in any wavelength range. The model allows us to solve the Simpson paradox, whereby the greenhouse effect (GHE has no temperature limit. On the contrary, we show that the temperature saturates, and its value depends primarily on the distance of the planet from the central star. We also show how the relative humidity affects the surface temperature of a planet and explain why the effect is smaller than the one derived when the above assumptions are neglected.

  8. Evaporative crystallization of salts from Electrodialysis concentrated brine at atmospheric and subatmospheric pressures

    Science.gov (United States)

    Wang, Dong; Du, Wei; Cheng, Penggao; Tang, Na; Wang, Xuekui

    2018-02-01

    A large amount of concentrated brine was produced as by-product during the process of the electrodialysis seawater desalination. In this study, the crystallization sequences of different salts from the brine through evaporative crystallization at both atmospheric and subatmospheric pressures were investigated in detail. The profile of the boiling temperature with density and the relationship between the boiling temperature and the pressure were recorded. The combination of Powder X-Ray Diffraction and the polarizing microscope was employed to identify the salts in the solid form. It can be inferred that NaCl crystallized out firstly and then MgSO4·6H2O and CaSO4 precipitate in order at both atmospheric and subatmospheric pressures, and it should be noticed that CaSO4 crystallized as anhydrate at 70°C and 90°C while as dihydrate at 50°C. At the end of all the experiments the precipitation rates of CaSO4 and NaCl have reached to more than 95% while MgSO4 only reached to about 60%.

  9. Distribution of air pollutants in the Inn Valley atmosphere during high concentration events in winter 2006

    International Nuclear Information System (INIS)

    Schnitzhofer, R.; Norman, M; Dunkl, J.; Wistaler, A.; Hansel, A.; Neininger, B.; Gohm, A.

    2006-01-01

    Full text: The goal of the INNOX field campaign, which took place during January and February 2006 near the town of Schwaz, was to obtain a three-dimensional picture of the spatial distribution of air pollutants in the Inn Valley during wintertime. For this purpose continuous ground based measurements and, on six chosen days, vertical profiles within the lowest 200 m above ground level (AGL) of the valley atmosphere of certain VOCs (benzene, toluene, etc.) and CO were performed using a proton-transfer-reaction mass spectrometry instrument (PTR-MS). For the soundings a 200-m long teflon line was fixed on a tethered balloon through which the air was sucked to the PTR-MS instrument and to a CO analyser. Next to the inlet on the tethered balloon meteorological data, such as air temperature, pressure, wind, were measured as well. Above the lowest 200 m AGL a research aircraft from MetAir AG (Switzerland), equipped with various instruments for in-situ measurements of air pollutants and meteorological data, was operated. A typical flight pattern consisted of five vertical cross sections between about 150 to 2500 m AGL and lasted about three hours. Altogether 25 hours of aircraft measurements were carried out on six different days. The combination of low-level balloon measurements and upper-level aircraft observations yields vertical profiles of various parameters which cover the whole valley atmosphere. Preliminary results which show strong vertical but also horizontal gradients of air pollutant concentrations will be presented. (author)

  10. Molecular dynamics simulation of the local concentration and structure in multicomponent aerosol nanoparticles under atmospheric conditions.

    Science.gov (United States)

    Karadima, Katerina S; Mavrantzas, Vlasis G; Pandis, Spyros N

    2017-06-28

    Molecular dynamics (MD) simulations were employed to investigate the local structure and local concentration in atmospheric nanoparticles consisting of an organic compound (cis-pinonic acid or n-C 30 H 62 ), sulfate and ammonium ions, and water. Simulations in the isothermal-isobaric (NPT) statistical ensemble under atmospheric conditions with a prespecified number of molecules of the abovementioned compounds led to the formation of a nanoparticle. Calculations of the density profiles of all the chemical species in the nanoparticle, the corresponding radial pair distribution functions, and their mobility inside the nanoparticle revealed strong interactions developing between sulfate and ammonium ions. However, sulfate and ammonium ions prefer to populate the central part of the nanoparticle under the simulated conditions, whereas organic molecules like to reside at its outer surface. Sulfate and ammonium ions were practically immobile; in contrast, the organic molecules exhibited appreciable mobility at the outer surface of the nanoparticle. When the organic compound was a normal alkane (e.g. n-C 30 H 62 ), a well-organized (crystalline-like) phase was rapidly formed at the free surface of the nanoparticle and remained separate from the rest of the species.

  11. Effect of atmosphere composition on the oxidation behavior of MCrAlY coatings

    Energy Technology Data Exchange (ETDEWEB)

    Song, P.; Subanovic, M.; Toscano, J.; Naumenko, D.; Quadakkers, W.J. [Forschungszentrum Juelich GmbH, Institute for Energy Research (IEF-2), 52425 Juelich (Germany)

    2011-07-15

    In the present work the effect of atmosphere composition on the growth rate and adherence of the alumina scales was studied using free-standing MCrAlY-coatings and TBC-specimens with MCrAlY-bondcoats. The exposures comprised isothermal and cyclic exposures in laboratory air and Ar-H{sub 2}-H{sub 2}O at 1100 C. It is shown that minor Zr-addition to the bondcoat results in enhanced scale growth and internal oxidation. This effect is independent of the atmosphere composition. As a consequence of the rapid oxide formation the times to TBC failure on the Zr-containing bondcoat in both atmospheres were much shorter compared to those with Zr-free bondcoat. In the latter case the formation of a thin compact alumina TGO was slower in H{sub 2}/H{sub 2}O than in air resulting in significantly longer TBC-lifetime in the former atmosphere. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  12. Time-scale invariant changes in atmospheric radon concentration and crustal strain prior to a large earthquake

    Directory of Open Access Journals (Sweden)

    Y. Kawada

    2007-01-01

    Full Text Available Prior to large earthquakes (e.g. 1995 Kobe earthquake, Japan, an increase in the atmospheric radon concentration is observed, and this increase in the rate follows a power-law of the time-to-earthquake (time-to-failure. This phenomenon corresponds to the increase in the radon migration in crust and the exhalation into atmosphere. An irreversible thermodynamic model including time-scale invariance clarifies that the increases in the pressure of the advecting radon and permeability (hydraulic conductivity in the crustal rocks are caused by the temporal changes in the power-law of the crustal strain (or cumulative Benioff strain, which is associated with damage evolution such as microcracking or changing porosity. As the result, the radon flux and the atmospheric radon concentration can show a temporal power-law increase. The concentration of atmospheric radon can be used as a proxy for the seismic precursory processes associated with crustal dynamics.

  13. assessment of concentration of air pollutants using analytical and numerical solution of the atmospheric diffusion equation

    International Nuclear Information System (INIS)

    Esmail, S.F.H.

    2011-01-01

    The mathematical formulation of numerous physical problems a results in differential equations actually partial or ordinary differential equations.In our study we are interested in solutions of partial differential equations.The aim of this work is to calculate the concentrations of the pollution, by solving the atmospheric diffusion equation(ADE) using different mathematical methods of solution. It is difficult to solve the general form of ADE analytically, so we use some assumptions to get its solution.The solutions of it depend on the eddy diffusivity profiles(k) and the wind speed u. We use some physical assumptions to simplify its formula and solve it. In the present work, we solve the ADE analytically in three dimensions using Green's function method, Laplace transform method, normal mode method and these separation of variables method. Also, we use ADM as a numerical method. Finally, comparisons are made with the results predicted by the previous methods and the observed data.

  14. Atmospheric concentrations and trends of poly- and perfluoroalkyl substances (PFAS) and volatile methyl siloxanes (VMS) over 7 years of sampling in the Global Atmospheric Passive Sampling (GAPS) network.

    Science.gov (United States)

    Rauert, Cassandra; Shoieb, Mahiba; Schuster, Jasmin K; Eng, Anita; Harner, Tom

    2018-07-01

    Poly- and per-fluoroalkyl substances (PFAS) and volatile methyl siloxanes (VMS) were monitored at 21 sites in the Global Atmospheric Passive Sampling (GAPS) Network. Atmospheric concentrations previously reported from 2009 were compared to concentrations measured at these sites in 2013 and 2015, to assess trends over 7 years of monitoring. Concentrations of the fluorotelomer alcohols (FTOHs) and fluorinated sulfonamides and sulfonamidoethanols (FOSAs and FOSEs) were stable at these sites from 2009 to 2015 with no significant difference (p > 0.05) in concentrations. Elevated concentrations of all the neutral PFAS were detected at the urban sites as compared to the polar/background sites. The perfluorosulfonic acids (PFSAs), meanwhile, saw a significant increase (p  0.05). Concentrations of the PFSAs and the PFCAs were similar at all location types, showing the global reach of these persistent compounds. Concentrations of the cyclic VMS (cVMS) were at least an order of magnitude higher than the linear VMS (lVMS) and the PFAS. Octamethylcyclotetrasiloxane (D4), decamethylcyclopentasiloxane (D5) and dodecamethylcyclohexasiloxane (D6) saw a weak significant increase in concentrations from 2009 to 2013 (p < 0.05), however, hexamethylcyclotrisiloxane (D3) had a strong significant decrease in concentrations from 2009 to 2015 (p < 0.01). Copyright © 2018 The Authors. Published by Elsevier Ltd.. All rights reserved.

  15. Results of concentration measurements of artificial radioactive aerosols in the lower atmosphere; Resultats des mesures de concentration, dans la basse atmosphere, des aerosols radioactifs artificiels

    Energy Technology Data Exchange (ETDEWEB)

    Ardouin, B; Jehanno, C; Labeyrie, J; Lambert, G; Tanaevsky, O; Vassy, E [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1963-07-01

    This report gives the results of the measurements of artificial gross-{beta}-radioactivity in aerosols in the lower atmosphere; these measurements have been made by the Electronic Physics Service of the Electronic Department, and by the Atmospheric Physics Laboratory of the Paris Science Faculty. The measurements were begun in September 1956 and were continued in an increasing number of stations both in France and in the rest of the world. The present report deals with the period up to the end of august 1961, that is up to the end of the nuclear moratorium. After recalling the constitution and the properties of radioactive aerosols present in the atmosphere, the authors describe the measurement methods, estimate their accuracy and discuss various aspects of the results. (authors) [French] Ce rapport contient les resultats des mesures de radioactivite {beta} globale d'origine artificielle des aerosols dans la basse atmosphere, effectuees conjointement par le Service d'Electronique Physique du Departement d'Electronique et le Laboratoire de Physique de l'Atmosphere de la Faculte des Sciences de Paris. Les mesures ont commence en septembre 1956 et ont ete poursuivies dans un nombre croissant de stations, tant en France que dans le reste du monde. Le present rapport s'arrete a la fin aout 1961, c'est-a-dire au moment de la reprise des essais nucleaires. Apres avoir rappele la constitution et les proprietes des aerosols radioactifs presents dans l'atmosphere, les auteurs indiquent les methodes de mesure utilisees, evaluent leur precision et discutent les differents aspects des resultats de leurs mesures. (auteurs)

  16. Monoterpene and herbivore-induced emissions from cabbage plants grown at elevated atmospheric CO 2 concentration

    Science.gov (United States)

    Vuorinen, Terhi; Reddy, G. V. P.; Nerg, Anne-Marja; Holopainen, Jarmo K.

    The warming of the lower atmosphere due to elevating CO 2 concentration may increase volatile organic compound (VOC) emissions from plants. Also, direct effects of elevated CO 2 on plant secondary metabolism are expected to lead to increased VOC emissions due to allocation of excess carbon on secondary metabolites, of which many are volatile. We investigated how growing at doubled ambient CO 2 concentration affects emissions from cabbage plants ( Brassica oleracea subsp. capitata) damaged by either the leaf-chewing larvae of crucifer specialist diamondback moth ( Plutella xylostella L.) or generalist Egyptian cotton leafworm ( Spodoptera littoralis (Boisduval)). The emission from cabbage cv. Lennox grown in both CO 2 concentrations, consisted mainly of monoterpenes (sabinene, limonene, α-thujene, 1,8-cineole, β-pinene, myrcene, α-pinene and γ-terpinene). ( Z)-3-Hexenyl acetate, sesquiterpene ( E, E)- α-farnesene and homoterpene ( E)-4,8-dimethyl-1,3,7-nonatriene (DMNT) were emitted mainly from herbivore-damaged plants. Plants grown at 720 μmol mol -1 of CO 2 had significantly lower total monoterpene emissions per shoot dry weight than plants grown at 360 μmol mol -1 of CO 2, while damage by both herbivores significantly increased the total monoterpene emissions compared to intact plants. ( Z)-3-Hexenyl acetate, ( E, E)- α-farnesene and DMNT emissions per shoot dry weight were not affected by the growth at elevated CO 2. The emission of DMNT was significantly enhanced from plants damaged by the specialist P. xylostella compared to the plants damaged by the generalist S. littoralis. The relative proportions of total monoterpenes and total herbivore-induced compounds of total VOCs did not change due to the growth at elevated CO 2, while insect damage increased significantly the proportion of induced compounds. The results suggest that VOC emissions that are induced by the leaf-chewing herbivores will not be influenced by elevated CO 2 concentration.

  17. 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 (PM 2.5 )-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 PM 2.5 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/m 3 ) 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/m 3 ) 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 PM 2.5 -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.

  18. Ten years of continual monitoring of 222Rn concentration in Bratislava atmosphere

    International Nuclear Information System (INIS)

    Holy, K.; Bosa, I.; Polaskova, A.; Boehm, R.; Ondo-Estok, D.; Bulko, M.; Hola, O.

    2003-01-01

    By the continual monitoring we obtained the extensive set of radon data in Bratislava atmosphere covering the time period of 1991 - 2000. The average annual radon activity concentrations varied from 4.1 to 7.2 Bq/m 3 . In the years 1996 - 1999 the decreasing of the average annual radon concentration was observed. The average daily courses of the radon activity concentration for individual months calculated on the basis of all data from 1991 - 2000 have a form of waves with the maximum in morning hours and with the minimum in the afternoon. The maximal amplitude of daily wave was found out in August (2.9 Bq/m 3 ) and minimal in December (0.5 Bq/m 3 ). The average daily wave obtained as the mean off all data from years 1991 - 2000 reaches the maximum between 4 and 6 a. m. and the minimum between 2 and 4 p. m. The Rn-222 activity concentration reaches its average daily value equal to 5.6 Bq/m 3 at about 10 a. m and at 9 p. m. The amplitude of average daily wave is equal to 1.5 Bq/m 3 . The average annual radon course calculated on the basis of all the measured data reaches the minimum in April and the maximum in October with seasonal variation from 3.9 to 6.9 Bq/m 3 . The annual radon courses differ from each other for various periods of the day. (authors)

  19. High-rate reduction of copper oxide using atmospheric-pressure inductively coupled plasma microjets

    International Nuclear Information System (INIS)

    Tajima, Satomi; Tsuchiya, Shouichi; Matsumori, Masashi; Nakatsuka, Shigeki; Ichiki, Takanori

    2011-01-01

    Reduction of copper oxide was performed using an atmospheric-pressure inductively coupled plasma (AP-ICP) microjet while varying the input power P between 15 and 50 W. Cuprous oxide (Cu 2 O) and cupric oxide (CuO) were formed on the sputtered Cu surface by thermal annealing. Dynamic behavior of the microplasma jet, optical emission from H atoms, the substrate temperature, chemical bonding states of the treated surface, and the thickness of the reduced Cu layer were measured to study the fundamental reduction process. Surface composition and the thickness of the reduced Cu layer changed significantly with P. Rapid reduction of CuO and Cu 2 O was achieved at a rate of 493 nm/min at P = 50 W since high-density H atoms were produced by the AP-ICP microjet.

  20. High-rate reduction of copper oxide using atmospheric-pressure inductively coupled plasma microjets

    Energy Technology Data Exchange (ETDEWEB)

    Tajima, Satomi; Tsuchiya, Shouichi [Department of Bioengineering, Graduate School of Engineering, University of Tokyo, 2-11-16 Yayoi, Bunkyo-ku, 113-8656 (Japan); Matsumori, Masashi; Nakatsuka, Shigeki [Panasonic Factory Solutions Co., Ltd., 2-7 Matsuba-cho, Kadoma-city, Osaka, 571-8502 (Japan); Ichiki, Takanori, E-mail: ichiki@sogo.t.u-tokyo.ac.jp [Department of Bioengineering, Graduate School of Engineering, University of Tokyo, 2-11-16 Yayoi, Bunkyo-ku, 113-8656 (Japan); Institute of Engineering Innovation, Graduate School of Engineering, University of Tokyo, 2-11-16 Yayoi, Bunkyo-ku, Tokyo, 113-8656 (Japan)

    2011-08-01

    Reduction of copper oxide was performed using an atmospheric-pressure inductively coupled plasma (AP-ICP) microjet while varying the input power P between 15 and 50 W. Cuprous oxide (Cu{sub 2}O) and cupric oxide (CuO) were formed on the sputtered Cu surface by thermal annealing. Dynamic behavior of the microplasma jet, optical emission from H atoms, the substrate temperature, chemical bonding states of the treated surface, and the thickness of the reduced Cu layer were measured to study the fundamental reduction process. Surface composition and the thickness of the reduced Cu layer changed significantly with P. Rapid reduction of CuO and Cu{sub 2}O was achieved at a rate of 493 nm/min at P = 50 W since high-density H atoms were produced by the AP-ICP microjet.

  1. Highly concentrated zinc oxide nanocrystals sol with strong blue emission

    International Nuclear Information System (INIS)

    Vafaee, M.; Sasani Ghamsari, M.; Radiman, S.

    2011-01-01

    Highly concentrated ZnO sol was synthesized by an improved sol-gel method. Water was used as a modifier to control the sol-gel reaction and provide a way to increase the sol concentration. Concentration of ZnO in the prepared sol is higher than from other methods. Optical absorption and photoluminescence were used to investigate optical properties of the prepared sol. FTIR test was performed to study the influence of water on the compounds of as-prepared sol. The size and morphology of ZnO nanoparticles have been studied by HRTEM. The prepared colloidal ZnO nanocrystals have narrow size distribution (5-8 nm) and showed strong blue emission. The prepared sol has enough potential for optoelectronic applications. - Research highlights: → Novel sol-gel route has been employed to prepare highly concentrated ZnO colloidal nanocrystals. → Water has been used to control the sources of emission in synthesized material. → A strong blue luminescent material has been obtained.

  2. Low-temperature plasma-catalytic oxidation of formaldehyde in atmospheric pressure gas streams

    International Nuclear Information System (INIS)

    Ding Huixian; Zhu Aimin; Lu Fugong; Xu Yong; Zhang Jing; Yang Xuefeng

    2006-01-01

    Formaldehyde (HCHO) is a typical air pollutant capable of causing serious health disorders in human beings. This work reports plasma-catalytic oxidation of formaldehyde in gas streams via dielectric barrier discharges over Ag/CeO 2 pellets at atmospheric pressure and 70 0 C. With a feed gas mixture of 276 ppm HCHO, 21.0% O 2 , 1.0% H 2 O in N 2 , ∼99% of formaldehyde can be effectively destructed with an 86% oxidative conversion into CO 2 at GHSV of 16500 h -1 and input discharge energy density of 108 J l -1 . At the same experimental conditions, the conversion percentages of HCHO to CO 2 from pure plasma-induced oxidation (discharges over fused silica pellets) and from pure catalytic oxidation over Ag/CeO 2 (without discharges) are 6% and 33% only. The above results and the CO plasma-catalytic oxidation experiments imply that the plasma-generated short-lived gas phase radicals, such as O and HO 2 , play important roles in the catalytic redox circles of Ag/CeO 2 to oxidize HCHO and CO to CO 2

  3. Concentrated Aqueous Sodium Tosylate as Green Medium for Alkene Oxidation and Nucleophilic Substitution Reactions.

    Science.gov (United States)

    Sela, Tal; Lin, Xiaoxi; Vigalok, Arkadi

    2017-11-03

    A hydrotropic solution of highly concentrated sodium tosylate (NaOTs) can be used as a recyclable medium for the environmentally benign oxidation of conjugated alkenes with H 2 O 2 . Both uncatalyzed and metal-catalyzed reactions provided the corresponding oxidation products in higher yields than in pure water or many common organic solvents.

  4. Response of biomass and nitrogen yield of white clover to radiation and atmospheric CO2 concentration

    International Nuclear Information System (INIS)

    Manderscheid, R.; Bender, J.; Schenk, U.; Weigel, H.J.

    1997-01-01

    The objectives of the present study were to test (i) whether the effect of season-long CO 2 enrichment on plant dry matter production of white clover (Trifolium repens cv. Karina) depends on the temperature or can solely be explained by changes in radiation use efficiency, and (ii) whether the atmospheric CO 2 concentration affects the relationship between tissue %N and plant biomass. Plants were grown in pots with adequate nutrient and water supply and were exposed to ambient and above ambient CO 2 concentrations (approximately +80 ppm, +160 ppm, +280 ppm) in open-top chambers for two seasons. Nitrogen fertilizer was given only before the experiment started to promote N 2 fixation. Plants were clipped to a height of 5 cm, when the canopy had reached a height of about 20 cm and when the CO 2 effect had not been diminished due to self-shading of the leaves. Photon exposure (400–700 nm) measured above the canopy was linearly related to the above ground biomass, the leaf area index and the nitrogen yield (r 2 > 0.94). The slopes of the curves depended on the CO 2 concentration. Since most of the radiation (>90%) was absorbed by the foliage, the slopes were used to calculate the CO 2 effect on the radiation use efficiency of biomass production, which is shown to increase curvilinearly between 380 and 660 ppm CO 2 from 2.7 g MJ −1 to 3.9 g MJ −1 . CO 2 enrichment increased above ground biomass by increasing the leaf number, the individual leaf weight and the leaf area; specific leaf weight was not affected. The relative CO 2 response varied between harvests; there was a slight but not significant positive relationship with mean daytime temperature. At the beginning of the season, plant nitrogen concentration in the above ground biomass was decreased by CO 2 enrichment. However, at later growth stages, when the plants depended solely on N 2 fixation, nitrogen concentration was found to be increased when the nitrogen concentration value was adjusted for the decrease

  5. Does carbon isotope data help explain atmospheric CO2 concentrations during glacial periods?

    International Nuclear Information System (INIS)

    Alverson, K.; Le Grand, P.

    2002-01-01

    An inverse ocean box modeling approach is used to address the question of what may have caused decreased atmospheric CO 2 concentration during glacial periods. The inverse procedure seeks solutions that are consistent, within prescribed uncertainties, with both available paleodata constraints and box model conservation equations while relaxing traditional assumptions such as exact steady state and precise prescription of uncertain model parameters. Decreased ventilation of Southern Ocean deep water, decreased Southern Ocean air-sea gas exchange, and enhanced high latitude biological pumping are all shown to be individually capable of explaining available paleodata constraints provided that significant calcium carbonate compensation is allowed. None of the scenarios require more than a very minor (order 1 deg. C) glacial reduction in low to mid latitude sea surface temperature although scenarios with larger changes are equally plausible. One explanation for the fairly wide range of plausible solutions is that most paleo-data directly constrain the inventory of paleo-tracers but only indirectly constrain their fluxes. Because the various scenarios that have been proposed to explain pCO 2 levels during the last glacial maximum are distinguished primarily by different fluxes, the data, including ocean 13 C concentrations, do not allow one to confidently chose between them. Oceanic 14 C data for the last glacial maximum, which can constrain water mass fluxes, present an excellent potential solution to this problem if their reliability is demonstrated in the future. (author)

  6. Simultaneous determination of Rn-220 and Rn-222 concentrations in atmospheres by cellulose nitrate ionographic detectors

    International Nuclear Information System (INIS)

    Lobao, N.

    1977-01-01

    A method for the indoor determination of airborne radon and radon daughters is described, based in the utilization of cellulose nitrate (CN) ionographic detectors (LR-115-Kodak-Pathe) These track-etching detectors are coupled to an air sample and to a difusion chamber respectively. In the first system ambient air is pulled through a fiber glass filter for collection of airborne radon daughters (Flow: 230 ml/min). In the second system, the cellulose nitrate detectors is coupled/min). In the second system, the cellulose nitrate detectors is coupled to a difusion chamber electrostatic precipitator arrangement. Here the CN detector will register only the alpha particles given off by the decay products of Rn-222 formed within the sensitive volume of electrostatic precipitator. The construction of calibration curves for the two systems using adequate steady-state concentrations of Rn-220 and Rn-222 in an exposure chamber (1 cubic meter), will allow the use of the system for measurement of measurement of averaged integrated radon concentrations. The CN attached to the CN attached to the air sampler is exposed in the reference atmosphere with and without a mylar filter for discrimination of alpha particles with different energies Field sampling indicated however, that efficiency of the two systems are still low for the measurement of environmental levels of Rn-220 and Rn-222 within houses of the AENR, recommendations for efficienty improvement of the system are proposed [pt

  7. Assessment of the performance of a compact concentric spectrometer system for Atmospheric Differential Optical Absorption Spectroscopy

    Science.gov (United States)

    Whyte, C.; Leigh, R. J.; Lobb, D.; Williams, T.; Remedios, J. J.; Cutter, M.; Monks, P. S.

    2009-12-01

    A breadboard demonstrator of a novel UV/VIS grating spectrometer has been developed based upon a concentric arrangement of a spherical meniscus lens, concave spherical mirror and curved diffraction grating suitable for a range of atmospheric remote sensing applications from the ground or space. The spectrometer is compact and provides high optical efficiency and performance benefits over traditional instruments. The concentric design is capable of handling high relative apertures, owing to spherical aberration and comma being near zero at all surfaces. The design also provides correction for transverse chromatic aberration and distortion, in addition to correcting for the distortion called "smile", the curvature of the slit image formed at each wavelength. These properties render this design capable of superior spectral and spatial performance with size and weight budgets significantly lower than standard configurations. This form of spectrometer design offers the potential for exceptionally compact instrument for differential optical absorption spectroscopy (DOAS) applications from LEO, GEO, HAP or ground-based platforms. The breadboard demonstrator has been shown to offer high throughput and a stable Gaussian line shape with a spectral range from 300 to 450 nm at 0.5 nm resolution, suitable for a number of typical DOAS applications.

  8. Assessment of the performance of a compact concentric spectrometer system for Atmospheric Differential Optical Absorption Spectroscopy

    Directory of Open Access Journals (Sweden)

    C. Whyte

    2009-12-01

    Full Text Available A breadboard demonstrator of a novel UV/VIS grating spectrometer has been developed based upon a concentric arrangement of a spherical meniscus lens, concave spherical mirror and curved diffraction grating suitable for a range of atmospheric remote sensing applications from the ground or space. The spectrometer is compact and provides high optical efficiency and performance benefits over traditional instruments. The concentric design is capable of handling high relative apertures, owing to spherical aberration and comma being near zero at all surfaces. The design also provides correction for transverse chromatic aberration and distortion, in addition to correcting for the distortion called "smile", the curvature of the slit image formed at each wavelength. These properties render this design capable of superior spectral and spatial performance with size and weight budgets significantly lower than standard configurations. This form of spectrometer design offers the potential for exceptionally compact instrument for differential optical absorption spectroscopy (DOAS applications from LEO, GEO, HAP or ground-based platforms. The breadboard demonstrator has been shown to offer high throughput and a stable Gaussian line shape with a spectral range from 300 to 450 nm at 0.5 nm resolution, suitable for a number of typical DOAS applications.

  9. Reconstruction of Atmospheric Tracer Releases with Optimal Resolution Features: Concentration Data Assimilation

    Science.gov (United States)

    Singh, Sarvesh Kumar; Turbelin, Gregory; Issartel, Jean-Pierre; Kumar, Pramod; Feiz, Amir Ali

    2015-04-01

    The fast growing urbanization, industrialization and military developments increase the risk towards the human environment and ecology. This is realized in several past mortality incidents, for instance, Chernobyl nuclear explosion (Ukraine), Bhopal gas leak (India), Fukushima-Daichi radionuclide release (Japan), etc. To reduce the threat and exposure to the hazardous contaminants, a fast and preliminary identification of unknown releases is required by the responsible authorities for the emergency preparedness and air quality analysis. Often, an early detection of such contaminants is pursued by a distributed sensor network. However, identifying the origin and strength of unknown releases following the sensor reported concentrations is a challenging task. This requires an optimal strategy to integrate the measured concentrations with the predictions given by the atmospheric dispersion models. This is an inverse problem. The measured concentrations are insufficient and atmospheric dispersion models suffer from inaccuracy due to the lack of process understanding, turbulence uncertainties, etc. These lead to a loss of information in the reconstruction process and thus, affect the resolution, stability and uniqueness of the retrieved source. An additional well known issue is the numerical artifact arisen at the measurement locations due to the strong concentration gradient and dissipative nature of the concentration. Thus, assimilation techniques are desired which can lead to an optimal retrieval of the unknown releases. In general, this is facilitated within the Bayesian inference and optimization framework with a suitable choice of a priori information, regularization constraints, measurement and background error statistics. An inversion technique is introduced here for an optimal reconstruction of unknown releases using limited concentration measurements. This is based on adjoint representation of the source-receptor relationship and utilization of a weight

  10. Toward Synchronous Evaluation of Source Apportionments for Atmospheric Concentration and Deposition of Sulfate Aerosol Over East Asia

    Science.gov (United States)

    Itahashi, S.

    2018-03-01

    Source apportionments for atmospheric concentration, dry deposition, and wet deposition of sulfate aerosol (SO42-) were synchronously evaluated over East Asia, a main source of anthropogenic sulfur dioxide (SO2) emissions. Estimating dry deposition was difficult owing to the difficulty of measuring deposition velocity directly; therefore, sensitivity simulations using two dry deposition schemes were conducted. Moreover, sensitivity simulations for different emission inventories, the largest uncertainty source in the air quality model, were also conducted. In total, four experimental settings were used. Model performance was verified for atmospheric concentration and wet deposition using a ground-based observation network in China, Korea, and Japan, and all four model settings captured the observations. The underestimation of wet deposition over China was improved by an adjusted approach that linearly scaled the modeled precipitation values to observations. The synchronous evaluation of source apportionments for atmospheric concentration and dry and wet deposition showed the dominant contribution of anthropogenic emissions from China to the atmospheric concentration and deposition in Japan. The contributions of emissions from volcanoes were more important for wet deposition than for atmospheric concentration. Differences in the dry deposition scheme and emission inventory did not substantially influence the relative ratio of source apportionments over Japan. Because the dry deposition was more attributed to local factors, the differences in dry deposition may be an important determinant of the source contributions from China to Japan. Verification of these findings, including the dry deposition velocity, is necessary for better understanding of the behavior of sulfur compound in East Asia.

  11. Atmospheric BTEX concentrations in the vicinity of the crude oil refinery of the Baltic region.

    Science.gov (United States)

    Baltrėnas, Pranas; Baltrėnaitė, Edita; Serevičienė, Vaida; Pereira, Paulo

    2011-11-01

    Among chemical industries, petroleum refineries have been identified as large emitters of a wide variety of pollutants. Benzene, toluene, ethylbenzene, and xylene (BTEX) form an important group of aromatic volatile organic compounds (VOCs) because of their role in the troposphere chemistry and the risk posed to human health. A very large crude oil refinery of the Baltic States (200,000 bbl/day) is situated in the northern, rural part of Lithuania, 10 km from the town of Mažeikiai (Lithuania). The objectives of this study were: (1) to determine of atmospheric levels of BTEX in the region rural and urban parts at the vicinity of the crude oil refinery; and (2) to investigate the effect of meteorological parameters (wind speed, wind direction, temperature, pressure, humidity) on the concentrations measured. The averaged concentration of benzene varied from 2.12 ppbv in the rural areas to 2.75 ppbv in the urban areas where the traffic was determined to be a dominant source of BTEX emissions. Our study showed that concentration of benzene, as strictly regulated air pollutant by EU Directive 2008/50/EC, did not exceed the limit of 5 ppbv in the region in the vicinity of the crude oil refinery during the investigated period. No significant change in air quality in the vicinity of the oil refinery was discovered, however, an impact of the industry on the background air quality was detected. The T/B ratio (0.50-0.81) that was much lower than 2.0, identified other sources of pollution than traffic.

  12. Indium tin oxide films prepared by atmospheric plasma annealing and their semiconductor-metal conductivity transition around room temperature

    International Nuclear Information System (INIS)

    Li Yali; Li Chunyang; He Deyan; Li Junshuai

    2009-01-01

    We report the synthesis of indium tin oxide (ITO) films using the atmospheric plasma annealing (APA) technique combined with the spin-coating method. The ITO film with a low resistivity of ∼4.6 x 10 -4 Ω cm and a high visible light transmittance, above 85%, was achieved. Hall measurement indicates that compared with the optimized ITO films deposited by magnetron sputtering, the above-mentioned ITO film has a higher carrier concentration of ∼1.21 x 10 21 cm -3 and a lower mobility of ∼11.4 cm 2 V -1 s -1 . More interestingly, these electrical characteristics result in the semiconductor-metal conductivity transition around room temperature for the ITO films prepared by APA.

  13. [Determination of the daily changes curve of nitrogen oxides in the atmosphere by digital imaging colorimetry method].

    Science.gov (United States)

    Yang, Chuan-Xiao; Sun, Xiang-Ying; Liu, Bin

    2009-06-01

    From the digital images of the red complex which resulted in the interaction of nitrite with N-(1-naphthyl) ethylenediamine dihydrochloride and P-Aminobenzene sulfonic acid, it could be seen that the solution colors obviously increased with increasing the concentration of nitrite ion. The JPEG format of the digital images was transformed into gray-scale format by origin 7.0 software, and the gray values were measured with scion image software. It could be seen that the gray values of the digital image obviously increased with increasing the concentration of nitrite ion, too. Thus a novel digital imaging colorimetric (DIC) method to determine nitrogen oxides (NO(x)) contents in air was developed. Based on the red, green and blue (RGB) tricolor theory, the principle of the digital imaging colorimetric method and the influential factors on digital imaging were discussed. The present method was successfully applied to the determination of the daily changes curve of nitrogen oxides in the atmosphere and NO2- in synthetic samples with the recovery of 97.3%-104.0%, and the relative standard deviation (RSD) was less than 5.0%. The results of the determination were consistent with those obtained by spectrophotometric method.

  14. The Effect of the Concentration of Oxidant, Cr(VI), on the Iron Oxidation in Saline Water

    Science.gov (United States)

    Ahn, H.; Jo, H. Y.; Ryu, J. H.; Koh, Y. K.

    2014-12-01

    Deep geological disposal is currently considered as the most appropriate method to isolate high level radioactive wastes (HLRWs) from the ecosystem. If groundwater seeps into underground disposal facilities, water molecules can be dissociated to radicals or peroxides, which can oxidize metal canisters and HLRWs. The oxidized radionuclides with a high solubility can be dissolved in the groundwater. Some dissolved radionuclides can act as oxidants. The continuous radiolysis of water molecules, which results from continuous seepage of groundwater, can enable the continuous production of the radioactive oxidants, resulting in an increase in concentration of oxidants. In this study, the effect of oxidant concentration on iron oxidation in the presence of salt was evaluated. Zero valent iron (ZVI) particles were reacted with Cr(VI) solutions with initial Cr(VI) concentrations ranged from 50 to 300 mg/L in reactors. The initial pH and NaCl concentration were fixed at 3 and 0.5 M, respectively. An increase in the initial Cr(VI) concentration caused an increase in the rate and extend of H2 gas production. The decrement of Cr(VI) was increased as the initial Cr(VI) concentration was increased. The penetration of H+ ions in the presence Cl- ions through the passive film on the ZVI particles caused the reaction between H+ ions and ZVI particles, producing H2 gas and Fe2+ ions. The passive film was damaged during the reaction due to the eruption of H2 gas or peptization by Cl- ions. The Fe2+ ions were reacted with Cr(VI) ions in the solution, producing Fe(III)-Cr(III) (oxy)hydroxides on the passive film of ZVI particles or in the solution as colloidal particles. The Fe(III)-Cr(III) (oxy)hydroxides tends to be precipitated as colloidal particles at a high Cr(VI) concentration and precipitated on the passive film at a low Cr(VI) concentration. The passive film was repaired or thickened by additional formation of Fe(III)-Cr(III) (oxy)hydroxides at a lower Cr(VI) concentration.

  15. Heterogeneous Oxidation of Atmospheric Organic Aerosol: Kinetics of Changes to the Amount and Oxidation State of Particle-Phase Organic Carbon.

    Science.gov (United States)

    Kroll, Jesse H; Lim, Christopher Y; Kessler, Sean H; Wilson, Kevin R

    2015-11-05

    Atmospheric oxidation reactions are known to affect the chemical composition of organic aerosol (OA) particles over timescales of several days, but the details of such oxidative aging reactions are poorly understood. In this study we examine the rates and products of a key class of aging reaction, the heterogeneous oxidation of particle-phase organic species by the gas-phase hydroxyl radical (OH). We compile and reanalyze a number of previous studies from our laboratories involving the oxidation of single-component organic particles. All kinetic and product data are described on a common basis, enabling a straightforward comparison among different chemical systems and experimental conditions. Oxidation chemistry is described in terms of changes to key ensemble properties of the OA, rather than to its detailed molecular composition, focusing on two quantities in particular, the amount and the oxidation state of the particle-phase carbon. Heterogeneous oxidation increases the oxidation state of particulate carbon, with the rate of increase determined by the detailed chemical mechanism. At the same time, the amount of particle-phase carbon decreases with oxidation, due to fragmentation (C-C scission) reactions that form small, volatile products that escape to the gas phase. In contrast to the oxidation state increase, the rate of carbon loss is nearly uniform among most systems studied. Extrapolation of these results to atmospheric conditions indicates that heterogeneous oxidation can have a substantial effect on the amount and composition of atmospheric OA over timescales of several days, a prediction that is broadly in line with available measurements of OA evolution over such long timescales. In particular, 3-13% of particle-phase carbon is lost to the gas phase after one week of heterogeneous oxidation. Our results indicate that oxidative aging represents an important sink for particulate organic carbon, and more generally that fragmentation reactions play a major

  16. Two-Step Oxidation of Refractory Gold Concentrates with Different Microbial Communities.

    Science.gov (United States)

    Wang, Guo-Hua; Xie, Jian-Ping; Li, Shou-Peng; Guo, Yu-Jie; Pan, Ying; Wu, Haiyan; Liu, Xin-Xing

    2016-11-28

    Bio-oxidation is an effective technology for treatment of refractory gold concentrates. However, the unsatisfactory oxidation rate and long residence time, which cause a lower cyanide leaching rate and gold recovery, are key factors that restrict the application of traditional bio-oxidation technology. In this study, the oxidation rate of refractory gold concentrates and the adaption of microorganisms were analyzed to evaluate a newly developed two-step pretreatment process, which includes a high temperature chemical oxidation step and a subsequent bio-oxidation step. The oxidation rate and recovery rate of gold were improved significantly after the two-step process. The results showed that the highest oxidation rate of sulfide sulfur could reach to 99.01 % with an extreme thermophile microbial community when the pulp density was 5%. Accordingly, the recovery rate of gold was elevated to 92.51%. Meanwhile, the results revealed that moderate thermophiles performed better than acidophilic mesophiles and extreme thermophiles, whose oxidation rates declined drastically when the pulp density was increased to 10% and 15%. The oxidation rates of sulfide sulfur with moderate thermophiles were 93.94% and 65.73% when the pulp density was increased to 10% and 15%, respectively. All these results indicated that the two-step pretreatment increased the oxidation rate of refractory gold concentrates and is a potential technology to pretreat the refractory sample. Meanwhile, owing to the sensitivity of the microbial community under different pulp density levels, the optimization of microbial community in bio-oxidation is necessary in industry.

  17. Increasing surface ozone concentrations in the background atmosphere of Southern China, 1994–2007

    Directory of Open Access Journals (Sweden)

    T. Wang

    2009-08-01

    Full Text Available Tropospheric ozone is of great importance with regard to air quality, atmospheric chemistry, and climate change. In this paper we report the first continuous record of surface ozone in the background atmosphere of South China. The data were obtained from 1994 to 2007 at a coastal site in Hong Kong, which is strongly influenced by the outflow of Asian continental air during the winter and the inflow of maritime air from the subtropics in the summer. Three methods are used to derive the rate of change in ozone. A linear fit to the 14-year record shows that the ozone concentration increased by 0.58 ppbv/yr, whereas comparing means in years 1994–2000 and 2001–2007 gives an increase of 0.87 ppbv/yr for a 7-year period. The ozone changes in air masses from various source regions are also examined. Using local wind and carbon monoxide (CO data to filter out local influence, we find that ozone increased by 0.94 ppbv/yr from 1994–2000 to 2001–2007 in air masses from Eastern China, with similar changes in the other two continent-influenced air-mass groups, but no statistically significant change in the marine air. An examination of the nitrogen dioxide (NO2 column obtained from GOME and SCIAMACHY reveals an increase in atmospheric NO2 in China's three fastest developing coastal regions, whereas NO2 in other parts of Asia decreased during the same period, and no obvious trend over the main shipping routes in the South China Sea was indicated. Thus the observed increase in background ozone in Hong Kong is most likely due to the increased emissions of NO2 (and possibly volatile organic compounds (VOCs as well in the upwind coastal regions of mainland China. The CO data at Hok Tsui showed less definitive changes compared to the satellite NO2 column. The increase in background ozone likely made a strong contribution (81% to the rate of increase in "total ozone" at an urban site in Hong Kong

  18. Oxidation of a new Biogenic VOC: Chamber Studies of the Atmospheric Chemistry of Methyl Chavicol

    Science.gov (United States)

    Bloss, William; Alam, Mohammed; Adbul Raheem, Modinah; Rickard, Andrew; Hamilton, Jacqui; Pereira, Kelly; Camredon, Marie; Munoz, Amalia; Vazquez, Monica; Vera, Teresa; Rodenas, Mila

    2013-04-01

    The oxidation of volatile organic compounds (VOCs) leads to formation of ozone and SOA, with consequences for air quality, health, crop yields, atmospheric chemistry and radiative transfer. Recent observations have identified Methyl Chavicol ("MC": Estragole; 1-allyl-4-methoxybenzene, C10H12O) as a major BVOC above pine forests in the USA, and oil palm plantations in Malaysian Borneo. Palm oil cultivation, and hence MC emissions, may be expected to increase with societal food and bio fuel demand. We present the results of a series of simulation chamber experiments to assess the atmospheric fate of MC. Experiments were performed in the EUPHORE facility, monitoring stable product species, radical intermediates, and aerosol production and composition. We determine rate constants for reaction of MC with OH and O3, and ozonolysis radical yields. Stable product measurements (FTIR, PTRMS, GC-SPME) are used to determine the yields of stable products formed from OH- and O3- initiated oxidation, and to develop an understanding of the initial stages of the MC degradation chemistry. A surrogate mechanism approach is used to simulate MC degradation within the MCM, evaluated in terms of ozone production measured in the chamber experiments, and applied to quantify the role of MC in the real atmosphere.

  19. NITROUS OXIDE BEHAVIOR IN THE ATMOSPHERE, AND IN COMBUSTION AND INDUSTRIAL SYSTEMS

    Science.gov (United States)

    Tropospheric measurements show that nitrous oxide (N2O) concentrations are increasing over time. This demonstrates the existence of one or more significant anthropogenic sources, a fact that has generated considerable research interest over the last several years. The debate has ...

  20. Nitrous oxide in the Schelde estuary: production by nitrification and emission to the atmosphere

    NARCIS (Netherlands)

    De Wilde, H.; De Bie, M.J.M.

    2000-01-01

    Concentrations of nitrous oxide (N2O), oxygen, nitrate, and ammonium, as well as nitrification activity were determined along the salinity gradient of the Schelde Estuary, Northwest Europe, in October 1993, March 1994, and July 1996, The entire estuary was always supersaturated with N2O.

  1. Tritium concentrations in the atmospheric environment at Rokkasho, Japan before the final testing of the spent nuclear fuel reprocessing plant

    International Nuclear Information System (INIS)

    Akata, Naofumi; Kakiuchi, Hideki; Shima, Nagayoshi; Iyogi, Takashi; Momoshima, Noriyuki; Hisamatsu, Shun'ichi

    2011-01-01

    This study aimed at obtaining background tritium concentrations in precipitation and air at Rokkasho where the first commercial spent nuclear fuel reprocessing plant in Japan has been under construction. Tritium concentration in monthly precipitation during fiscal years 2001-2005 had a seasonal variation pattern which was high in spring and low in summer. The tritium concentration was higher than that observed at Chiba City as a whole. The seasonal peak concentration at Rokkasho was generally higher than that at Chiba City, while the baseline concentrations of both were similar. The reason for the difference may be the effect of air mass from the Asian continent which is considered to have high tritium concentration. Atmospheric tritium was operationally separated into HTO, HT and hydrocarbon (CH 3 T) fractions, and the samples collected every 3 d-14 d during fiscal year 2005 were analyzed for these fractions. The HTO concentration as radioactivity in water correlated well with that in the precipitation samples. The HT concentration was the highest among the chemical forms analyzed, followed by the HTO and CH 3 T concentrations. The HT and CH 3 T concentrations did not have clear seasonal variation patterns. The HT concentration followed the decline previously reported by Mason and Ostlund with an apparent half-life of 4.8 y. The apparent and environmental half-lives of CH 3 T were estimated as 9.2 y and 36.5 y, respectively, by combining the present data with literature data. The Intergovernmental Panel on Climate Change used the atmospheric lifetime of 12 y for CH 4 to estimate global warming in its 2007 report. The longer environmental half-life of CH 3 T suggested its supply from other sources than past nuclear weapon testing in the atmosphere. - Highlights: → We observed background tritium concentrations in atmospheric environment at Rokkasho, Japan. → Tritium concentration in precipitation was high in spring and low in summer. → The atmospheric HT

  2. Tritium concentrations in the atmospheric environment at Rokkasho, Japan before the final testing of the spent nuclear fuel reprocessing plant

    Energy Technology Data Exchange (ETDEWEB)

    Akata, Naofumi, E-mail: nao@ies.or.jp [Department of Radioecology, Institute for Environmental Sciences, 1-7 Ienomae, Obuchi, Rokkasho, Aomori 039-3212 (Japan); Kakiuchi, Hideki [Department of Radioecology, Institute for Environmental Sciences, 1-7 Ienomae, Obuchi, Rokkasho, Aomori 039-3212 (Japan); Shima, Nagayoshi [Entex Inc., 1-2-8 Asahi, Kashiwa, Chiba 277-0852 (Japan); Iyogi, Takashi [Department of Radioecology, Institute for Environmental Sciences, 1-7 Ienomae, Obuchi, Rokkasho, Aomori 039-3212 (Japan); Momoshima, Noriyuki [Radioisotope Center, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581 (Japan); Hisamatsu, Shun' ichi [Department of Radioecology, Institute for Environmental Sciences, 1-7 Ienomae, Obuchi, Rokkasho, Aomori 039-3212 (Japan)

    2011-09-15

    This study aimed at obtaining background tritium concentrations in precipitation and air at Rokkasho where the first commercial spent nuclear fuel reprocessing plant in Japan has been under construction. Tritium concentration in monthly precipitation during fiscal years 2001-2005 had a seasonal variation pattern which was high in spring and low in summer. The tritium concentration was higher than that observed at Chiba City as a whole. The seasonal peak concentration at Rokkasho was generally higher than that at Chiba City, while the baseline concentrations of both were similar. The reason for the difference may be the effect of air mass from the Asian continent which is considered to have high tritium concentration. Atmospheric tritium was operationally separated into HTO, HT and hydrocarbon (CH{sub 3}T) fractions, and the samples collected every 3 d-14 d during fiscal year 2005 were analyzed for these fractions. The HTO concentration as radioactivity in water correlated well with that in the precipitation samples. The HT concentration was the highest among the chemical forms analyzed, followed by the HTO and CH{sub 3}T concentrations. The HT and CH{sub 3}T concentrations did not have clear seasonal variation patterns. The HT concentration followed the decline previously reported by Mason and Ostlund with an apparent half-life of 4.8 y. The apparent and environmental half-lives of CH{sub 3}T were estimated as 9.2 y and 36.5 y, respectively, by combining the present data with literature data. The Intergovernmental Panel on Climate Change used the atmospheric lifetime of 12 y for CH{sub 4} to estimate global warming in its 2007 report. The longer environmental half-life of CH{sub 3}T suggested its supply from other sources than past nuclear weapon testing in the atmosphere. - Highlights: > We observed background tritium concentrations in atmospheric environment at Rokkasho, Japan. > Tritium concentration in precipitation was high in spring and low in summer. > The

  3. Oxidation Behavior of Titanium Carbonitride Coating Deposited by Atmospheric Plasma Spray Synthesis

    Science.gov (United States)

    Zhu, Lin; He, Jining; Yan, Dianran; Liao, Hanlin; Zhang, Nannan

    2017-10-01

    As a high-hardness and anti-frictional material, titanium carbonitride (TiCN) thick coatings or thin films are increasingly being used in many industrial fields. In the present study, TiCN coatings were obtained by atmospheric plasma spray synthesis or reactive plasma spray. In order to promote the reaction between the Ti particles and reactive gases, a home-made gas tunnel was mounted on a conventional plasma gun to perform the spray process. The oxidation behavior of the TiCN coatings under different temperatures in static air was carefully investigated. As a result, when the temperature was over 700 °C, the coatings suffered from serious oxidation, and finally they were entirely oxidized to the TiO2 phase at 1100 °C. The principal oxidation mechanism was clarified, indicating that the oxygen can permeate into the defects and react with TiCN at high temperatures. In addition, concerning the use of a TiCN coating in high-temperature conditions, the microhardness of the oxidized coatings at different treatment temperatures was also evaluated.

  4. Effects of land use on the concentration and emission of nitrous oxide in nitrogen-enriched rivers.

    Science.gov (United States)

    Yang, Libiao; Lei, Kun

    2018-07-01

    Nitrous oxide (N 2 O) is a potent greenhouse gas that contributes to climate change and stratospheric ozone destruction. Nitrogen-enriched rivers are significant sources of atmospheric N 2 O. This study conducted a one-year field campaign in seven N-enriched rivers draining urban, rural, and agricultural land to determine the link between the production, concentrations, and emissions of N 2 O and land use. Estimated N 2 O fluxes varied between 1.30 and 1164.38 μg N 2 O-N m -2 h -1 with a mean value of 154.90 μg N 2 O-N m -2 h -1 , indicating that rivers were the net sources of atmospheric N 2 O. Concentrations of N 2 O ranged between 0.23 and 29.21 μg N 2 O-N L -1 with an overall mean value of 3.81 μg N 2 O-N L -1 . Concentrations of ammonium and nitrate in urban and rural rivers were high in the cold season. The concentrations were also high in agricultural rivers in the wet season. N 2 O concentrations and emissions in rural and urban rivers followed a similar pattern to ammonium and a similar pattern to nitrate in agricultural rivers. A strong link between the concentrations and emissions of N 2 O and land use was observed. N 2 O concentrations in and emissions from the rivers draining the urban and rural areas were significantly higher than the rivers draining the agricultural areas (P Nitrate-N and NO 3- -O isotope data and linear regression of N 2 O and river water variables strongly indicated that dissolved N 2 O was mainly derived from nitrification in agricultural rivers and denitrification in rural and urban rivers. Copyright © 2018 Elsevier Ltd. All rights reserved.

  5. USING POLYMERIC HYDROGEN GETTERS TO PREVENT COMBUSTIBLE ATMOSPHERES DURING INTERIM SAFE STORAGE OF PLUTONIUM OXIDE

    International Nuclear Information System (INIS)

    Woodsmall, T

    2007-01-01

    Nuclear Materials Management (NMM) of WSRC has recently installed the capability to perform both non-destructive and destructive examination of 3013 containers of Pu oxide in accordance with DOE-STD-3013. The containers will be opened and the oxide will be sampled for analysis. The remaining bulk oxide must then be safely stored in a non-3013-compliant configuration. Available processing equipment and controls cannot prevent the oxide from adsorbing moisture during this process. Subsequent radiolysis of moisture during storage may generate combustible quantities of gases while waiting final processing, and satisfying DOE Interim Safe Storage Criteria (ISSC) would require that storage containers be vented at impractical frequencies. With support from an independent National Laboratory, WSRC/NMM has demonstrated that a commercial hydrogen getter material will effectively prevent the accumulation of combustible gas concentrations. A project overview, including storage requirements and strategies, as well as getter technology, current test results, and anticipated future developments will be addressed

  6. Gaschromatographic proof of nitrous oxide concentrations in air by means of radiation ionization detectors

    International Nuclear Information System (INIS)

    Popp, P.; Schoentube, E.; Oppermann, G.

    1985-01-01

    For the analysis of nitrous oxide concentrations at workplaces in operating theatres, gaschromatography is a particularly suitable method if it is possible to measure nitrous oxide concentrations in the ppm to ppb region. For this, most frequently used gaschromatographic detectors (flame ionization detector, thermal conductivity detector) are unsuitable, whereas radiation ionization detectors can be used successfully. The investigations using detectors designed at the Central Institute for Isotopes and Radiation Research of the GDR Academy of Sciences showed that a high-temperature electron-capture detector (ECD), working at a temperatur of 250 0 C, enables the determination of traces of nitrous oxide with a detection limit of about 200 ppb, while the helium detector has a limit of 50 ppb of nitrous oxide in room air. Since the helium detector requires extremely pure carrier gas, the high-temperature ECD appears more suitable for analyzing nitrous oxide. (author)

  7. Electro-oxidation of reverse osmosis concentrates generated in tertiary water treatment.

    Science.gov (United States)

    Pérez, G; Fernández-Alba, A R; Urtiaga, A M; Ortiz, I

    2010-05-01

    This work investigates the application of the electro-oxidation technology provided with boron doped diamond (BDD), an electrode material which has shown outstanding properties in oxidation of organic and inorganic compounds, for the treatment of reverse osmosis (RO) concentrates generated in tertiary wastewater treatment plants (WWTP). Chemical oxygen demand (COD), ammonium and several anions were measured during the electro-oxidation process, and the influence of the applied current density (20-200A/m(2)) was analysed on process kinetics. Analytical assessment showed that several emerging pollutants (pharmaceuticals, personal care products, stimulants, etc.) were presented both in the effluent of the secondary WWTP as well as in the RO concentrate. For this reason, a group of 10 emerging pollutants, those found with higher concentrations, was selected in order to test whether electro-oxidation can be also applied for their mitigation. In the removal of emerging pollutants the electrical current density in the range 20-100A/m(2) did not show influence likely due to the mass transfer resistance developed in the process when the oxidized solutes are present in such low concentrations. Their removal rates were fitted to first order expressions, and the apparent kinetic constants for the anodic oxidation of each compound were calculated. Finally, the formation of trihalomethanes (THMs) has been checked; concluding that after selecting the appropriate operational conditions the attained concentration is lower than the standards for drinking water established in European and EPA regulations. Copyright (c) 2010 Elsevier Ltd. All rights reserved.

  8. Air mass origins by back trajectory analysis for evaluating atmospheric 210Pb concentrations at Rokkasho, Aomori, Japan

    International Nuclear Information System (INIS)

    Akata, N.; Kawabata, H.; Hasegawa, H.; Kondo, K.; Chikuchi, Y.; Hisamatsu, S.; Inaba, J.; Sato, T.

    2009-01-01

    Atmospheric concentrations of 210 Pb change with various factors such as meso-scale meteorological conditions. We have already reported the biweekly atmospheric 210 Pb concentrations in Rokkasho, Japan for 5 years and found that they had clear seasonal variations: low concentrations in summer and high values in winter to spring. To study the reasons for the seasonal variations, the origins of the air mass flowing to Rokkasho were analyzed by 3-D backward air mass trajectory analysis. Routes of the calculated trajectories were classified into four regions: northeastern and southeastern Asian Continent, sea and other regions. The atmospheric 210 Pb concentrations were well correlated with the frequency of the routes through the northeastern Asian Continent. A non-linear multiple regression analysis of the 210 Pb concentrations and the relative frequencies of the four routes showed good fitting of the predicted values to the observed ones, and indicated that the atmospheric 210 Pb concentrations in Rokkasho depended on the frequency of the air mass from the northeastern Asian Continent. (author)

  9. Enhanced oxidation of arsenite to arsenate using tunable K+ concentration in the OMS-2 tunnel.

    Science.gov (United States)

    Hou, Jingtao; Sha, Zhenjie; Hartley, William; Tan, Wenfeng; Wang, Mingxia; Xiong, Juan; Li, Yuanzhi; Ke, Yujie; Long, Yi; Xue, Shengguo

    2018-03-29

    Cryptomelane-type octahedral molecular sieve manganese oxide (OMS-2) possesses high redox potential and has attracted much interest in its application for oxidation arsenite (As(III)) species of arsenic to arsenate (As(V)) to decrease arsenic toxicity and promote total arsenic removal. However, coexisting ions such as As(V) and phosphate are ubiquitous and readily bond to manganese oxide surface, consequently passivating surface active sites of manganese oxide and reducing As(III) oxidation. In this study, we present a novel strategy to significantly promote As(III) oxidation activity of OMS-2 by tuning K + concentration in the tunnel. Batch experimental results reveal that increasing K + concentration in the tunnel of OMS-2 not only considerably improved As(III) oxidation kinetics rate from 0.027 to 0.102 min -1 , but also reduced adverse effect of competitive ion on As(III) oxidation. The origin of K + concentration effect on As(III) oxidation was investigated through As(V) and phosphate adsorption kinetics, detection of Mn 2+ release in solution, surface charge characteristics, and density functional theory (DFT) calculations. Experimental results and theoretical calculations confirm that by increasing K + concentration in the OMS-2 tunnel not only does it improve arsenic adsorption on K + doped OMS-2, but also accelerates two electrons transfers from As(III) to each bonded Mn atom on OMS-2 surface, thus considerably improving As(III) oxidation kinetics rate, which is responsible for counteracting the adverse adsorption effects by coexisting ions. Copyright © 2018 Elsevier Ltd. All rights reserved.

  10. Measurements of the oxidation state and concentration of plutonium in interstitial waters of the Irish Sea

    International Nuclear Information System (INIS)

    Nelson, D.M.; Lovett, M.B.

    1980-01-01

    The question of plutonium movement in interstitial waters resulting from diffusion along concentration gradients or from advective flow is addressed. The results of measurements of both the concentration and the oxidation state of plutonium in interstitial water collected from sediments near the Windscale discharge, in the solid phases of these sediments and in seawater and suspended solids collected at the coring locations are discussed

  11. Oxygen dynamics in the aftermath of the Great Oxidation of Earth’s atmosphere

    DEFF Research Database (Denmark)

    Canfield, Donald Eugene; Ngombi-Pemba, Lauriss; Hammarlund, Emma

    2013-01-01

    -oxygenated deep waters whereas the youngest were deposited in euxinic waters, which were globally extensive. These fluctuations in oxygenation were likely driven by the comings and goings of the Lomagundi carbon isotope excursion, the longest–lived positive δ13C excursion in Earth history, generating a huge......The oxygen content of Earth’s atmosphere has varied greatly through time, progressing from exceptionally low levels before about 2.3 billion years ago, to much higher levels afterward. In the absence of better information, we usually view the progress in Earth’s oxygenation as a series of steps...... oxygen source to the atmosphere. As the Lomagundi event waned, the oxygen source became a net oxygen sink as Lomagundi organic matter became oxidized, driving oxygen to low levels; this state may have persisted for 200 million years....

  12. The determination of carbon dioxide concentration using atmospheric pressure ionization mass spectrometry/isotopic dilution and errors in concentration measurements caused by dryers.

    Science.gov (United States)

    DeLacy, Brendan G; Bandy, Alan R

    2008-01-01

    An atmospheric pressure ionization mass spectrometry/isotopically labeled standard (APIMS/ILS) method has been developed for the determination of carbon dioxide (CO(2)) concentration. Descriptions of the instrumental components, the ionization chemistry, and the statistics associated with the analytical method are provided. This method represents an alternative to the nondispersive infrared (NDIR) technique, which is currently used in the atmospheric community to determine atmospheric CO(2) concentrations. The APIMS/ILS and NDIR methods exhibit a decreased sensitivity for CO(2) in the presence of water vapor. Therefore, dryers such as a nafion dryer are used to remove water before detection. The APIMS/ILS method measures mixing ratios and demonstrates linearity and range in the presence or absence of a dryer. The NDIR technique, on the other hand, measures molar concentrations. The second half of this paper describes errors in molar concentration measurements that are caused by drying. An equation describing the errors was derived from the ideal gas law, the conservation of mass, and Dalton's Law. The purpose of this derivation was to quantify errors in the NDIR technique that are caused by drying. Laboratory experiments were conducted to verify the errors created solely by the dryer in CO(2) concentration measurements post-dryer. The laboratory experiments verified the theoretically predicted errors in the derived equations. There are numerous references in the literature that describe the use of a dryer in conjunction with the NDIR technique. However, these references do not address the errors that are caused by drying.

  13. Options for cost-effectively reducing atmospheric methane concentrations from anthropogenic biomass sources

    International Nuclear Information System (INIS)

    Roos, K.F.; Jacobs, C.; Orlic, M.

    1993-01-01

    Methane is a major greenhouse gas, second only to carbon dioxide in its contribution to future global warming. Methane concentrations have more than doubled over the last two centuries and continue to rise annually. These increases are largely correlated with increasing human populations. Methane emissions from human related activities currently account for about 70 percent of annual emissions. Of these human related emissions, biomass sources account for about 75 percent and non-biomass sources about 25 percent. Because methane has a shorter lifetime than other major greenhouse gases, efforts to reduce methane emissions may fairly quickly be translated into lower atmospheric concentrations of methane and lower levels of radiative forcing. This fairly quick response would have the benefit of slowing the rate of climate change and hence allow natural ecosystems more time to adapt. Importantly, methane may be cost-effectively reduced from a number of biomass and non-biomass sources in the United States and worldwide. Methane is a valuable fuel, not just a waste by-product, and often systems may be reconfigured to reap the fuel value of the methane and more than justify the necessary expenditures. Such options for reducing methane emission from biomass sources exist for landfills, livestock manures, and ruminant livestock, and have been implemented to varying degrees in countries around the world. However, there are a number of barriers that hinder the more widespread use of technologies, including institutional, financial, regulatory, informational, and other barriers. This paper describes an array of available options that may be cost-effectively implemented to reduce methane emissions from biomass sources. This paper also discusses a number of programs that have been developed in the United States and internationally to promote the implementation of these methane reduction options and overcome existing barriers

  14. 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.

  15. Effects of long-term elevated atmospheric CO2 concentrations on Pinus ponderosa

    International Nuclear Information System (INIS)

    Surano, K.A.; Kercher, J.R.

    1993-01-01

    This report details the results from an experiment of the effects of long-term elevated atmospheric CO 2 concentrations on ponderosa pine (Pinus ponderosa Laws.) saplings and seedlings. The study began in 1983 as a pilot study designed to explore the feasibility of using open-top chambers for continuous multi-year exposures on sapling-sized trees and to examine possible CO 2 responses so that future research could be adequately designed. however, following the first year of exposure, preliminary results from the study indicated that measurements of CO 2 responses should be intensified. Open-top chambers proved suitable for use in multiyear exposures of mature trees. With respect to the preliminary examination of CO 2 responses, many interesting observations were made. The nature of the preliminary results suggests that future long-term field CO 2 exposures on perennial species may be critical to the understanding and preparation for future environments. Other research reported here attempted to adapt an existing western coniferous forest growth and succession model for use in elevated CO 2 scenarios using differential species responses, and assessed the usefulness of the model in that regard. Seven papers have been processed separately for inclusion in the appropriate data bases

  16. Ship-Based Measurements of Atmospheric Mercury Concentrations over the Baltic Sea

    Directory of Open Access Journals (Sweden)

    Hanna Hoglind

    2018-02-01

    Full Text Available Mercury is a toxic pollutant emitted from both natural sources and through human activities. A global interest in atmospheric mercury has risen ever since the discovery of the Minamata disease in 1956. Properties of gaseous elemental mercury enable long range transport, which can cause pollution even in pristine environments. Gaseous elemental mercury (GEM was measured from winter 2016 to spring 2017 over the Baltic Sea. A Tekran 2357A mercury analyser was installed aboard the research and icebreaking vessel Oden for the purpose of continuous measurements of gaseous mercury in ambient air. Measurements were performed during a campaign along the Swedish east coast and in the Bothnian Bay near Lulea during the icebreaking season. Data was evaluated from Gothenburg using plotting software, and back trajectories for air masses were calculated. The GEM average of 1.36 ± 0.054 ng/m3 during winter and 1.29 ± 0.140 ng/m3 during spring was calculated as well as a total average of 1.36 ± 0.16 ng/m3. Back trajectories showed a possible correlation of anthropogenic sources elevating the mercury background level in some areas. There were also indications of depleted air, i.e., air with lower concentrations than average, being transported from the Arctic to northern Sweden, resulting in a drop in GEM levels.

  17. Effects of long-term elevated atmospheric CO{sub 2} concentrations on Pinus ponderosa

    Energy Technology Data Exchange (ETDEWEB)

    Surano, K.A.; Kercher, J.R. [eds.

    1993-10-01

    This report details the results from an experiment of the effects of long-term elevated atmospheric CO{sub 2} concentrations on ponderosa pine (Pinus ponderosa Laws.) saplings and seedlings. The study began in 1983 as a pilot study designed to explore the feasibility of using open-top chambers for continuous multi-year exposures on sapling-sized trees and to examine possible CO{sub 2} responses so that future research could be adequately designed. however, following the first year of exposure, preliminary results from the study indicated that measurements of CO{sub 2} responses should be intensified. Open-top chambers proved suitable for use in multiyear exposures of mature trees. With respect to the preliminary examination of CO{sub 2} responses, many interesting observations were made. The nature of the preliminary results suggests that future long-term field CO{sub 2} exposures on perennial species may be critical to the understanding and preparation for future environments. Other research reported here attempted to adapt an existing western coniferous forest growth and succession model for use in elevated CO{sub 2} scenarios using differential species responses, and assessed the usefulness of the model in that regard. Seven papers have been processed separately for inclusion in the appropriate data bases.

  18. VVER vessel steel corrosion at interaction with molten corium in oxidizing atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Bechta, S.V. [Alexandrov Research Institute of Technologies (NITI), Sosnovy Bor (Russian Federation)], E-mail: bechta@sbor.spb.su; Granovsky, V.S.; Khabensky, V.B.; Krushinov, E.V.; Vitol, S.A.; Sulatsky, A.A. [Alexandrov Research Institute of Technologies (NITI), Sosnovy Bor (Russian Federation); Gusarov, V.V.; Almiashev, V.I. [Institute of Silicate Chemistry, Russian Academy of Sciences (ISCh RAS), St. Petersburg (Russian Federation); Lopukh, D.B. [SPb State Electrotechnical University (SPbGETU), St. Petersburg (Russian Federation); Bottomley, D. [EUROPAISCHE KOMMISSION, Joint Research Centre Institut fuer Transurane (ITU), Karlsruhe (Germany); Fischer, M. [AREVA NP GmbH, Erlangen (Germany); Piluso, P. [CEA/DEN/DSNI, Saclay (France); Miassoedov, A.; Tromm, W. [Forschungszentrum Karlsruhe, Karlsruhe (Germany); Altstadt, E. [Forschungszentrum Rossendorf (FZR), Dresden (Germany); Fichot, F. [IRSN/DPAM/SEMCA, St. Paul lez Durance (France); Kymalainen, O. [FORTUM Nuclear Services Ltd., Espoo (Finland)

    2009-06-15

    The long-term in-vessel corium retention (IVR) in the lower head bears a risk of the vessel wall deterioration caused by steel corrosion. The ISTC METCOR Project has studied physicochemical impact of prototypic coria having different compositions in air and steam and has generated valuable experimental data on vessel steel corrosion. It is found that the corrosion rate is sensitive to corium composition, but the composition of oxidizing above-melt atmosphere (air, steam) has practically no influence on it. A model of the corrosion process that integrates the experimental data, is proposed and used for development of correlations.

  19. VVER vessel steel corrosion at interaction with molten corium in oxidizing atmosphere

    International Nuclear Information System (INIS)

    Bechta, S.V.; Granovsky, V.S.; Khabensky, V.B.; Krushinov, E.V.; Vitol, S.A.; Sulatsky, A.A.; Gusarov, V.V.; Almiashev, V.I.; Lopukh, D.B.; Bottomley, D.; Fischer, M.; Piluso, P.; Miassoedov, A.; Tromm, W.; Altstadt, E.; Fichot, F.; Kymalainen, O.

    2009-01-01

    The long-term in-vessel corium retention (IVR) in the lower head bears a risk of the vessel wall deterioration caused by steel corrosion. The ISTC METCOR Project has studied physicochemical impact of prototypic coria having different compositions in air and steam and has generated valuable experimental data on vessel steel corrosion. It is found that the corrosion rate is sensitive to corium composition, but the composition of oxidizing above-melt atmosphere (air, steam) has practically no influence on it. A model of the corrosion process that integrates the experimental data, is proposed and used for development of correlations.

  20. Self-sustained carbon monoxide oxidation oscillations on size-selected platinum nanoparticles at atmospheric pressure

    DEFF Research Database (Denmark)

    Jensen, Robert; Andersen, Thomas; Nierhoff, Anders Ulrik Fregerslev

    2013-01-01

    High-quality mass spectrometry data of the oscillatory behavior of CO oxidation on SiO2 supported Pt-nanoparticles at atmospheric pressure have been acquired as a function of pressure, coverage, gas composition and nanoparticle size. The oscillations are self-sustained for several days at constant......, temperature, pressure and CO/O2 ratio. The frequency of the oscillations is very well defined and increases over time. The oscillation frequency is furthermore strongly temperature dependent with increasing temperature resulting in increasing frequency. A plausible mechanism for the oscillations is proposed...

  1. Atmospheric concentrations of halogenated flame retardants at two remote locations: The Canadian High Arctic and the Tibetan Plateau

    International Nuclear Information System (INIS)

    Xiao Hang; Shen Li; Su, Yushan; Barresi, Enzo; DeJong, Maryl; Hung, Hayley; Lei, Ying-Duan; Wania, Frank; Reiner, Eric J.; Sverko, Ed; Kang, Shi-Chang

    2012-01-01

    Atmospheric concentrations of halogenated flame retardants (FRs) were monitored for approximately one year at two remote stations, namely Nam Co on the Tibetan Plateau and Alert in the Canadian High Arctic. BDE-47 and 99 were the dominant polybrominated diphenyl ether (PBDE) congeners at both sites. Atmospheric PBDE concentrations in Nam Co were generally lower than those at Alert. While significant seasonal variations were observed for PBDEs at Alert, the FR concentrations at Nam Co showed no significant seasonality, even though air masses originated from distinctly different regions during different seasons. This suggests that FRs in Tibet do not have regional sources, but are reflective of truly global background contamination. Three new FRs, namely 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE), 2-ethyl-1-hexyl-2,3,4,5-tetrabromobenzoate (EHTeBB) and bis(2-ethyl-1-hexyl)tetrabromophthalate (TBPH) were detected at relatively high concentrations at both sites. This is the first report of these FRs in the remote global atmosphere and suggests significant potential for long-range atmospheric transport. - Highlights: ► First year-round measurements of FRs in the atmosphere of the Tibetan Plateau. ► PBDEs in Tibet are reflective of truly global background levels. ► Orographic precipitation limits the transport of particle-bound chemicals. ► First study of BTBPE, EHTeBB and TBPH in the Arctic and Tibetan air. ► These new FRs may have significant long-range atmospheric transport potential. - Several brominated flame retardants (BTBPE, EHTeBB, TBPH) were present in the atmosphere of the Arctic and the Tibetan Plateau at levels similar to those of the PBDEs.

  2. Application of argon atmospheric cold plasma for indium tin oxide (ITO) based diodes

    Science.gov (United States)

    Akbari Nia, S.; Jalili, Y. Seyed; Salar Elahi, A.

    2017-09-01

    Transparent Conductive Oxide (TCO) layers due to transparency, high conductivity and hole injection capability have attracted a lot of attention. One of these layers is Indium Tin Oxide (ITO). ITO due to low resistance, transparency in the visible spectrum and its proper work function is widely used in the manufacture of organic light emitting diodes and solar cells. One way for improving the ITO surface is plasma treatment. In this paper, changes in surface morphology, by applying argon atmospheric pressure cold plasma, was studied through Atomic Force Microscopic (AFM) image analysis and Fourier Transform Infrared Spectroscopy (FTIR) analysis. FTIR analysis showed functional groups were not added or removed, but chemical bond angle and bonds strength on the surface were changed and also AFM images showed that surface roughness was increased. These factors lead to the production of diodes with enhanced Ohmic contact and injection mechanism which are more appropriate in industrial applications.

  3. CLIMATE CHANGE. Long-term climate forcing by atmospheric oxygen concentrations.

    Science.gov (United States)

    Poulsen, Christopher J; Tabor, Clay; White, Joseph D

    2015-06-12

    The percentage of oxygen in Earth's atmosphere varied between 10% and 35% throughout the Phanerozoic. These changes have been linked to the evolution, radiation, and size of animals but have not been considered to affect climate. We conducted simulations showing that modulation of the partial pressure of oxygen (pO2), as a result of its contribution to atmospheric mass and density, influences the optical depth of the atmosphere. Under low pO2 and a reduced-density atmosphere, shortwave scattering by air molecules and clouds is less frequent, leading to a substantial increase in surface shortwave forcing. Through feedbacks involving latent heat fluxes to the atmosphere and marine stratus clouds, surface shortwave forcing drives increases in atmospheric water vapor and global precipitation, enhances greenhouse forcing, and raises global surface temperature. Our results implicate pO2 as an important factor in climate forcing throughout geologic time. Copyright © 2015, American Association for the Advancement of Science.

  4. [Condition optimization for bio-oxidation of high-S and high-As gold concentrate].

    Science.gov (United States)

    Yang, Caiyun; Dong, Bowen; Wang, Meijun; Ye, Zhiyong; Zheng, Tianling; Huang, Huaiguo

    2015-12-04

    To study the effects of temperature and lixivium return on the concentrate bio-oxidation and rate of gold cyanide leaching. The bioleaching of a high-sulphur (S) and high-arsenic (As) refractory gold concentrate was conducted, and we studied the effects of different temperature (40 ° and 45 °C) and lixivium return (0 and 600 mL) on the bio-oxidation efficiency. The bacterial community structure also was investigated by 16S rRNA gene clone library. The results showed that both the temperature and lixivium return significantly influenced the oxidation system. The temperature rising elevated the oxidation level, while the addition of lixivium depressed the oxidation. Dissimilarity and DCA (detrended correspondence analysis) indicated the effect of temperature on oxidation system was much greater than lixivium. The bacterial community was comprised by Acidithiocacillus caldu (71%) Leptospirillum ferriphilum (23%) and Sulfobacillus thermosulfidooxidans (6%) indicated by the clone library, and the OTU coverage based on 97% sequence similarity was as high as 93.67%. Temperature rising to 45 T would improve the oxidation efficiency while lixivium return would decrease it. This study is helpful to provide an important guiding value for the industry cost optimization of mesophile bacterial oxidation and reduction process.

  5. A highly oxidized atmosphere-ocean system and oceanic molybdenum drawdown during the Paleoproterozoic

    Science.gov (United States)

    Goto, K. T.; Ito, T.; Suzuki, K.; Anbar, A. D.; Gordon, G. W.; Kashiwabara, T.; Takaya, Y.; Shimoda, G.; Nozaki, T.; Kiyokawa, S.; Tetteh, G. M.; Nyame, F. K.

    2014-12-01

    Multiple lines of evidence suggest that the first major oxidation of the atmosphere-ocean system occurred during the Paleoproterozoic. However, the course of this redox transition remains elusive. A number of large Mn deposits are distributed in Paleoproterozoic sedimentary successions. As Mn is a redox-sensitive element characterized by high redox potential, knowledge of the Mn cycle in Paleoproterozoic seawater may provide insight into redox evolution during this period. Here, we investigate the Mn cycle in Paleoproterozoic seawater based on the Re-Os and Mo isotope compositions, and the abundance of major and trace elements, in Mn-rich sedimentary rocks from the Nsuta deposit of the Birimian Supergroup, Ghana. The Mn ore is composed mainly of rhodochrosite and is distributed at the boundaries between sedimentary rocks and tholeiitic volcanic rocks. The Re-Os isochron age (2217 ± 100 Ma) we obtained was consistent with U-Pb zircon ages of the volcanic rocks. The manganophile elements, except for Mo, show no enrichment, which is similar to modern hydrothermal Mn oxides. The PAAS-normalized REE compositions show positive Ce anomaly, indicative of Ce enrichment due to the oxidation of Ce(III) by Mn(IV). These findings suggest that Mn ore formed from primary precipitation of Mn oxides from hydrothermal fluids as they were mixed with bottom seawater at ~2.2 Ga. Thus, the bottom seawater would have been sufficiently oxygenated for the precipitation of Mn oxides at ~2.2 Ga. The Nsuta ore samples exhibit slight Mo enrichment, but Mo/Mn ratios are orders of magnitude lower than those in modern hydrothermal Mn oxides. We also found that the Mo isotopes in the Nsuta ore are ~0.7‰ heavier than those in modern hydrothermal and hydrogenous Mn oxides. As Mo in hydrothermal Mn oxides is sourced primarily from seawater (Goto et al., in prep), these results may reflect smaller oceanic Mo inventory and heavier seawater Mo isotope composition at 2.2 Ga than those of present

  6. Methyl chavicol: characterization of its biogenic emission rate, abundance, and oxidation products in the atmosphere

    Directory of Open Access Journals (Sweden)

    N. C. Bouvier-Brown

    2009-03-01

    Full Text Available We report measurements of ambient atmospheric mixing ratios for methyl chavicol and determine its biogenic emission rate. Methyl chavicol, a biogenic oxygenated aromatic compound, is abundant within and above Blodgett Forest, a ponderosa pine forest in the Sierra Nevada Mountains of California. Methyl chavicol was detected simultaneously by three in-situ instruments – a gas chromatograph with mass spectrometer detector (GC-MS, a proton transfer reaction mass spectrometer (PTR-MS, and a thermal desorption aerosol GC-MS (TAG – and found to be abundant within and above Blodgett Forest. Methyl chavicol atmospheric mixing ratios are strongly correlated with 2-methyl-3-buten-2-ol (MBO, a light- and temperature-dependent biogenic emission from the ponderosa pine trees at Blodgett Forest. Scaling from this correlation, methyl chavicol emissions account for 4–68% of the carbon mass emitted as MBO in the daytime, depending on the season. From this relationship, we estimate a daytime basal emission rate of 0.72–10.2 μgCg−1 h−1, depending on needle age and seasonality. We also present the first observations of its oxidation products (4-methoxybenzaldehyde and 4-methyoxy benzene acetaldehyde in the ambient atmosphere. Methyl chavicol is a major essential oil component of many plant species. This work suggests that methyl chavicol plays a significant role in the atmospheric chemistry of Blodgett Forest, and potentially other sites, and should be included explicitly in both biogenic volatile organic carbon emission and atmospheric chemistry models.

  7. Tritium concentrations in the atmospheric environment at Rokkasho, Japan before the final testing of the spent nuclear fuel reprocessing plant.

    Science.gov (United States)

    Akata, Naofumi; Kakiuchi, Hideki; Shima, Nagayoshi; Iyogi, Takashi; Momoshima, Noriyuki; Hisamatsu, Shun'ichi

    2011-09-01

    This study aimed at obtaining background tritium concentrations in precipitation and air at Rokkasho where the first commercial spent nuclear fuel reprocessing plant in Japan has been under construction. Tritium concentration in monthly precipitation during fiscal years 2001-2005 had a seasonal variation pattern which was high in spring and low in summer. The tritium concentration was higher than that observed at Chiba City as a whole. The seasonal peak concentration at Rokkasho was generally higher than that at Chiba City, while the baseline concentrations of both were similar. The reason for the difference may be the effect of air mass from the Asian continent which is considered to have high tritium concentration. Atmospheric tritium was operationally separated into HTO, HT and hydrocarbon (CH(3)T) fractions, and the samples collected every 3 d-14 d during fiscal year 2005 were analyzed for these fractions. The HTO concentration as radioactivity in water correlated well with that in the precipitation samples. The HT concentration was the highest among the chemical forms analyzed, followed by the HTO and CH(3)T concentrations. The HT and CH(3)T concentrations did not have clear seasonal variation patterns. The HT concentration followed the decline previously reported by Mason and Östlund with an apparent half-life of 4.8 y. The apparent and environmental half-lives of CH(3)T were estimated as 9.2 y and 36.5 y, respectively, by combining the present data with literature data. The Intergovernmental Panel on Climate Change used the atmospheric lifetime of 12 y for CH(4) to estimate global warming in its 2007 report. The longer environmental half-life of CH(3)T suggested its supply from other sources than past nuclear weapon testing in the atmosphere. Copyright © 2011 Elsevier Ltd. All rights reserved.

  8. Future concentrations of atmospheric greenhouse gases CO2, CFC and CH4 - an assessment on the educational level

    International Nuclear Information System (INIS)

    Hoppenau, S.

    1992-01-01

    A model on the educational level is described to estimate effective future atmospheric CO 2 concentrations. The effects of chlorofluorocarbon and methane emission and deforestation are taken into account. The influence of different emission scenarios on the time evolution of greenhouse-gas concentration are illustrated. Future global energy policies are discussed both under the aspects of rising world population and the reduction in global CO 2 emissions. The model can be handled on a PC or even on a pocket calculator

  9. Relating Nimbus-7 37 GHz data to global land-surface evaporation, primary productivity and the atmospheric CO2 concentration

    Science.gov (United States)

    Choudhury, B. J.

    1988-01-01

    Global observations at 37 GHz by the Nimbus-7 SMMR are related to zonal variations of land surface evaporation and primary productivity, as well as to temporal variations of atmospheric CO2 concentration. The temporal variation of CO2 concentration and the zonal variations of evaporation and primary productivity are shown to be highly correlated with the satellite sensor data. The potential usefulness of the 37-GHz data for global biospheric and climate studies is noted.

  10. Atmospheric concentration of 210Pb in East Asia and its contribution to Japanese islands by long-range transport

    International Nuclear Information System (INIS)

    Doi, Taeko; Sato, Shin; Sato, Jun

    2007-01-01

    Atmospheric 210 Pb is a long-lived progeny of 222 Rn generated from the earth's crust and exists as adsorbed onto the surface of aerosol particles. The distribution of atmospheric 210 Pb in East Asia reflects (1) the concentration levels in continental and maritime air masses and (2) the spatial extent of the continental air mass. This paper reviews the previously observed results on seasonal variation of 210 Pb concentration at several sites of Japan, Korea and China to evaluate the contribution of continental to Japanese atmosphere, and the specific activity of 210 Pb in the main components of aerosol samples and discusses from the view point of the Japanese islands. The authors conclude that aerosols from continental East Asia in winter contain more soil particles with low specific radioactivity of 210 Pb than the aerosols in Japan and that the natural radionuclide is extremely useful tracer for researches on meteorological phenomena and global transfer of environmental pollution. (S. Ohno)

  11. Linking activity, composition and seasonal dynamics of atmospheric methane oxidizers in a meadow soil

    Science.gov (United States)

    Shrestha, Pravin Malla; Kammann, Claudia; Lenhart, Katharina; Dam, Bomba; Liesack, Werner

    2012-01-01

    Microbial oxidation is the only biological sink for atmospheric methane. We assessed seasonal changes in atmospheric methane oxidation and the underlying methanotrophic communities in grassland near Giessen (Germany), along a soil moisture gradient. Soil samples were taken from the surface layer (0–10 cm) of three sites in August 2007, November 2007, February 2008 and May 2008. The sites showed seasonal differences in hydrological parameters. Net uptake rates varied seasonally between 0 and 70 μg CH4 m−2 h−1. Greatest uptake rates coincided with lowest soil moisture in spring and summer. Over all sites and seasons, the methanotrophic communities were dominated by uncultivated methanotrophs. These formed a monophyletic cluster defined by the RA14, MHP and JR1 clades, referred to as upland soil cluster alphaproteobacteria (USCα)-like group. The copy numbers of pmoA genes ranged between 3.8 × 105–1.9 × 106 copies g−1 of soil. Temperature was positively correlated with CH4 uptake rates (P50 vol% and primarily related to members of the MHP clade. PMID:22189499

  12. Linking activity, composition and seasonal dynamics of atmospheric methane oxidizers in a meadow soil.

    Science.gov (United States)

    Shrestha, Pravin Malla; Kammann, Claudia; Lenhart, Katharina; Dam, Bomba; Liesack, Werner

    2012-06-01

    Microbial oxidation is the only biological sink for atmospheric methane. We assessed seasonal changes in atmospheric methane oxidation and the underlying methanotrophic communities in grassland near Giessen (Germany), along a soil moisture gradient. Soil samples were taken from the surface layer (0-10 cm) of three sites in August 2007, November 2007, February 2008 and May 2008. The sites showed seasonal differences in hydrological parameters. Net uptake rates varied seasonally between 0 and 70 μg CH(4) m(-2) h(-1). Greatest uptake rates coincided with lowest soil moisture in spring and summer. Over all sites and seasons, the methanotrophic communities were dominated by uncultivated methanotrophs. These formed a monophyletic cluster defined by the RA14, MHP and JR1 clades, referred to as upland soil cluster alphaproteobacteria (USCα)-like group. The copy numbers of pmoA genes ranged between 3.8 × 10(5)-1.9 × 10(6) copies g(-1) of soil. Temperature was positively correlated with CH(4) uptake rates (P50 vol% and primarily related to members of the MHP clade.

  13. Abiotic mechanism for the formation of atmospheric nitrous oxide from ammonium nitrate.

    Science.gov (United States)

    Rubasinghege, Gayan; Spak, Scott N; Stanier, Charles O; Carmichael, Gregory R; Grassian, Vicki H

    2011-04-01

    Nitrous oxide (N2O) is an important greenhouse gas and a primary cause of stratospheric ozone destruction. Despite its importance, there remain missing sources in the N2O budget. Here we report the formation of atmospheric nitrous oxide from the decomposition of ammonium nitrate via an abiotic mechanism that is favorable in the presence of light, relative humidity and a surface. This source of N2O is not currently accounted for in the global N2O budget. Annual production of N2O from atmospheric aerosols and surface fertilizer application over the continental United States from this abiotic pathway is estimated from results of an annual chemical transport simulation with the Community Multiscale Air Quality model (CMAQ). This pathway is projected to produce 9.3(+0.7/-5.3) Gg N2O annually over North America. N2O production by this mechanism is expected globally from both megacities and agricultural areas and may become more important under future projected changes in anthropogenic emissions.

  14. Indoor-outdoor nitric oxide and nitrogen dioxide concentrations at three sites in Riyadh, Saudi Arabia

    Energy Technology Data Exchange (ETDEWEB)

    Rowe, D.R. (D.R. Rowe Engineering Services, Inc., Bowling Green, KY (United States)); Al-Dhowalia, K.H.; Mansour, M.E. (King Saud Univ., Riyadh (Saudi Arabia))

    1991-08-01

    The objective of this study was to evaluate the nitric oxide and nitrogen oxide concentrations indoors and outdoors at three sites in Riyadh, Saudi Arabia. Results show that the outdoor and indoor concentrations for NO were at least 270 and 16 times the reported average worldwide NO concentrations, respectively. The NO(sub 2) concentrations were about 14 times reported outdoor worldwide levels; however, NO(sub 2) concentrations indoors were generally below those reported in the literature. The data presented, in combination with information presented in previous articles, will provide a valuable background database for use in dispersion models to determine the effect of the Kuwaiti oil well fires on the air quality of Riyadh.

  15. Concentrations and (delta)13C values of atmospheric CO2 from oceanic atmosphere through time: polluted and non-polluted areas

    International Nuclear Information System (INIS)

    Longinelli, Antonio; Selmo, Enrico; Lenaz, Renzo; Ori, Carlo

    2005-01-01

    CO 2 is one of the primary agents of global climate changes. The increase of atmospheric CO 2 concentration is essentially related to human-induced emissions and, particularly, to the burning of fossil fuel whose (delta) 13 C values are quite negative. Consequently, an increase of the CO 2 concentration in the atmosphere should be paralleled by a decrease of its (delta) 13 C. Continuous and/or spot measurements of CO 2 concentrations were repeatedly carried out during the last decade and in the same period of the year along hemispheric courses from Italy to Antarctica on a vessel of the Italian National Research Program in Antarctica. During these expeditions, discrete air samples were also collected in 4-l Pyrex flasks in order to carry out precise carbon isotope analyses on atmospheric CO 2 from different areas, including theoretically 'clean' open ocean areas, with the main purpose of comparing these open ocean results with the results obtained by the National Oceanic and Atmospheric Administration/World Meteorological Organization (NOAA/WMO) at land-based stations. According to the data obtained for these two variables, a relatively large atmospheric pollution is apparent in the Mediterranean area where the CO 2 concentration has reached the value of 384 ppmv while quite negative (delta) 13 C values have been measured only occasionally. In this area, southerly winds probably help to reduce the effect of atmospheric pollution even though, despite a large variability of CO 2 concentrations, these values are consistently higher than those measured in open ocean areas by a few ppmv to about 10 ppmv. A marked, though non-continuous, pollution is apparent in the area of the Bab-el-Mandeb strait where (delta) 13 C values considerably more negative than in the Central and Southern Red Sea were measured. The concentration of atmospheric CO 2 over the Central Indian Ocean increased from about 361 ppmv at the end of 1996 to about 373 ppmv at the end of 2003 (mean growth

  16. Oxidative Pressure Leaching of Silver from Flotation Concentrates with Ammonium Thiocyanate Solution

    Science.gov (United States)

    Yang, Sheng-Hai; Yang, Jian-Guang; Liu, Wei; Chen, Geng-Tao; Tang, Mo-Tang; Qiu, Guan-Zhou

    2010-02-01

    The thermodynamics and technologies of the selective pressure leaching of silver from flotation concentrates were investigated in an ammonium thiocyanate medium. Thermodynamic analyses, which include silver solubility in NH4SCN solution and Eh-pH diagrams of the Me-MeS-NH4SCN-H2O system at 25 °C, were discussed. The effects of several factors, such as temperature, leaching time, oxidant, pH value, flotation concentrates concentration, surfactant concentration, and so on, on the extraction percentages of silver and zinc were investigated. The following optimal leaching conditions were obtained: NH4SCN concentration 1.5 M, lignin concentration 0.5 g/L, Fe3+ concentration 2 g/L, flotation concentrates addition 200 g/L, and oxygen pressure 1.2 MPa at 130 °C for 3 hours. Under these optimum conditions, the average extraction percentage of silver exceeded 94 pct, whereas the average extraction percentage of zinc was less than 3 pct. Only 7 pct of ammonium thiocyanate was consumed after 4 cycles, which indicated that ammonium thiocyanate hardly was oxidized under these oxidative pressure leaching conditions.

  17. Transcriptional Response of the Archaeal Ammonia Oxidizer Nitrosopumilus maritimus to Low and Environmentally Relevant Ammonia Concentrations

    OpenAIRE

    Nakagawa, Tatsunori; Stahl, David A.

    2013-01-01

    The ability of chemoautotrophic ammonia-oxidizing archaea to compete for ammonia among marine microorganisms at low ambient concentrations has been in part attributed to their extremely high affinity for ammonia, but as yet there is no mechanistic understanding of supporting metabolism. We examined transcription of selected genes for anabolic functions (CO2 fixation, ammonia transport, and cell wall synthesis) and a central catabolic function (ammonia oxidation) in the thaumarchaeon Nitrosopu...

  18. A reduced order model to analytically infer atmospheric CO2 concentration from stomatal and climate data

    Science.gov (United States)

    Konrad, Wilfried; Katul, Gabriel; Roth-Nebelsick, Anita; Grein, Michaela

    2017-06-01

    To address questions related to the acceleration or deceleration of the global hydrological cycle or links between the carbon and water cycles over land, reliable data for past climatic conditions based on proxies are required. In particular, the reconstruction of palaeoatmospheric CO2 content (Ca) is needed to assist the separation of natural from anthropogenic Ca variability and to explore phase relations between Ca and air temperature Ta time series. Both Ta and Ca are needed to fingerprint anthropogenic signatures in vapor pressure deficit, a major driver used to explain acceleration or deceleration phases in the global hydrological cycle. Current approaches to Ca reconstruction rely on a robust inverse correlation between measured stomatal density in leaves (ν) of many plant taxa and Ca. There are two methods that exploit this correlation: The first uses calibration curves obtained from extant species assumed to represent the fossil taxa, thereby restricting the suitable taxa to those existing today. The second is a hybrid eco-hydrological/physiological approach that determines Ca with the aid of systems of equations based on quasi-instantaneous leaf-gas exchange theories and fossil stomatal data collected along with other measured leaf anatomical traits and parameters. In this contribution, a reduced order model (ROM) is proposed that derives Ca from a single equation incorporating the aforementioned stomatal data, basic climate (e.g. temperature), estimated biochemical parameters of assimilation and isotope data. The usage of the ROM is then illustrated by applying it to isotopic and anatomical measurements from three extant species. The ROM derivation is based on a balance between the biochemical demand and atmospheric supply of CO2 that leads to an explicit expression linking stomatal conductance to internal CO2 concentration (Ci) and Ca. The resulting expression of stomatal conductance from the carbon economy of the leaf is then equated to another

  19. Elevated atmospheric carbon dioxide concentration: effects of increased carbon input in a Lolium perenne soil on microorganisms and decomposition

    NARCIS (Netherlands)

    Ginkel, van J.H.; Gorissen, A.; Polci, D.

    2000-01-01

    Effects of ambient and elevated atmospheric CO2 concentrations (350 and 700 μl l-1) on net carbon input into soil, the production of root-derived material and the subsequent microbial transformation were investigated. Perennial ryegrass plants (L. perenne L.) were labelled in a continuously labelled

  20. Modeling concentrations and fluxes of atmospheric CO2 in the North East Atlantic region

    DEFF Research Database (Denmark)

    Geels, C.; Christensen, J.H.; Hansen, A.W.

    2001-01-01

    As part of the Danish NEAREX project a three-dimensional Eulerian hemispheric air pollution model is used to study the transport and concentrations of atmospheric CO2 in the North East Atlantic region. The model domain covers the major part of the Northern Hemisphere and currently the model...

  1. Desulfurization from thiophene by SO(4)(2-)/ZrO(2) catalytic oxidation at room temperature and atmospheric pressure.

    Science.gov (United States)

    Wang, Bo; Zhu, Jianpeng; Ma, Hongzhu

    2009-05-15

    Thiophene, due to its poison, together with its combustion products which causes air pollution and highly toxic characteristic itself, attracted more and more attention to remove from gasoline and some high concentration systems. As the purpose of achieving the novel method of de-thiophene assisted by SO(4)(2-)/ZrO(2) (SZ), three reactions about thiophene in different atmosphere at room temperature and atmospheric pressure were investigated. SO(4)(2-)/ZrO(2) catalyst were synthesized and characterized by X-ray photoelectron spectroscopy (XPS), Fourier transformation infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and scanning electron microscope (SEM). The products were detected by gas chromatography-mass spectrometry (GC-MS). XP spectra show that ozone-catalyst system (SZO) have two forms of sulfur element (S(6+) and S(2-)) on the catalyst surface, which distinguished from that of air-catalyst system (SZA) and blank-catalyst system (SZB) (S(6+)). And the results of GC-MS exhibited that some new compounds has been produced under this extremely mild condition. Especially, many kinds of sulfur compounds containing oxygen, that is easier to be extracted by oxidative desulfurization (ODS), have been detected in the SZA-1.5h and SZB-3h system. In addition, some long chain hydrocarbons have also been detected. While in SZO-0.5h system, only long chain hydrocarbons were found. The results show that total efficiency of desulfurization from thiophene with ozone near to 100% can be obtained with the SO(4)(2-)/ZrO(2) catalytic oxidation reaction.

  2. Desulfurization from thiophene by SO42-/ZrO2 catalytic oxidation at room temperature and atmospheric pressure

    International Nuclear Information System (INIS)

    Wang Bo; Zhu Jianpeng; Ma Hongzhu

    2009-01-01

    Thiophene, due to its poison, together with its combustion products which causes air pollution and highly toxic characteristic itself, attracted more and more attention to remove from gasoline and some high concentration systems. As the purpose of achieving the novel method of de-thiophene assisted by SO 4 2- /ZrO 2 (SZ), three reactions about thiophene in different atmosphere at room temperature and atmospheric pressure were investigated. SO 4 2- /ZrO 2 catalyst were synthesized and characterized by X-ray photoelectron spectroscopy (XPS), Fourier transformation infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and scanning electron microscope (SEM). The products were detected by gas chromatography-mass spectrometry (GC-MS). XP spectra show that ozone-catalyst system (SZO) have two forms of sulfur element (S 6+ and S 2- ) on the catalyst surface, which distinguished from that of air-catalyst system (SZA) and blank-catalyst system (SZB) (S 6+ ). And the results of GC-MS exhibited that some new compounds has been produced under this extremely mild condition. Especially, many kinds of sulfur compounds containing oxygen, that is easier to be extracted by oxidative desulfurization (ODS), have been detected in the SZA-1.5 h and SZB-3 h system. In addition, some long chain hydrocarbons have also been detected. While in SZO-0.5 h system, only long chain hydrocarbons were found. The results show that total efficiency of desulfurization from thiophene with ozone near to 100% can be obtained with the SO 4 2- /ZrO 2 catalytic oxidation reaction

  3. A novel advanced oxidation process——wet electrocatalytic oxidation for high concentrated organic wastewater treatment

    Institute of Scientific and Technical Information of China (English)

    DAI QiZhou; ZHOU MingHua; LEI LeCheng; ZHANG Xing Wang

    2007-01-01

    A novel advanced oxidation process-wet electrocatalytic oxidation(WEO)was studied with p-nitrophenol as model pollutant and β-PbO2 electrode as the anode.Compared with the effect of the individual wet air oxidation(WAO)and electrochemical oxidation(EO),the effect of WEO showed synergistic effect on COD removal under the conditions of temperature 160℃,C=1000mg·L-1,PN2=0.50MPa,Po2=0.9 MPa,current density=3 mA·cm-2,Na2SO4 3 g·L-1.And the synergistic factor got the best value of 0.98 within 120 min after 180 min treatment.The synergistic factor was studied after 120 min treatment at 100℃,120℃,140℃and 160℃,and the effect of 120℃was the best with the value of 1.26.Possible mechanism for the synergistic effect was discussed based on the analysis of free-radical generation and intermediates detected by HPLC and GC/MS.

  4. Rising atmospheric CO2 concentration may imply higher risk of Fusarium mycotoxin contamination of wheat grains.

    Science.gov (United States)

    Bencze, Szilvia; Puskás, Katalin; Vida, Gyula; Karsai, Ildikó; Balla, Krisztina; Komáromi, Judit; Veisz, Ottó

    2017-08-01

    Increasing atmospheric CO 2 concentration not only has a direct impact on plants but also affects plant-pathogen interactions. Due to economic and health-related problems, special concern was given thus in the present work to the effect of elevated CO 2 (750 μmol mol -1 ) level on the Fusarium culmorum infection and mycotoxin contamination of wheat. Despite the fact that disease severity was found to be not or little affected by elevated CO 2 in most varieties, as the spread of Fusarium increased only in one variety, spike grain number and/or grain weight decreased significantly at elevated CO 2 in all the varieties, indicating that Fusarium infection generally had a more dramatic impact on the grain yield at elevated CO 2 than at the ambient level. Likewise, grain deoxynivalenol (DON) content was usually considerably higher at elevated CO 2 than at the ambient level in the single-floret inoculation treatment, suggesting that the toxin content is not in direct relation to the level of Fusarium infection. In the whole-spike inoculation, DON production did not change, decreased or increased depending on the variety × experiment interaction. Cooler (18 °C) conditions delayed rachis penetration while 20 °C maximum temperature caused striking increases in the mycotoxin contents, resulting in extremely high DON values and also in a dramatic triggering of the grain zearalenone contamination at elevated CO 2 . The results indicate that future environmental conditions, such as rising CO 2 levels, may increase the threat of grain mycotoxin contamination.

  5. Atmospheric CO2 concentration effects on rice water use and biomass production.

    Directory of Open Access Journals (Sweden)

    Uttam Kumar

    Full Text Available Numerous studies have addressed effects of rising atmospheric CO2 concentration on rice biomass production and yield but effects on crop water use are less well understood. Irrigated rice evapotranspiration (ET is composed of floodwater evaporation and canopy transpiration. Crop coefficient Kc (ET over potential ET, or ETo is crop specific according to FAO, but may decrease as CO2 concentration rises. A sunlit growth chamber experiment was conducted in the Philippines, exposing 1.44-m2 canopies of IR72 rice to four constant CO2 levels (195, 390, 780 and 1560 ppmv. Crop geometry and management emulated field conditions. In two wet (WS and two dry (DS seasons, final aboveground dry weight (agdw was measured. At 390 ppmv [CO2] (current ambient level, agdw averaged 1744 g m-2, similar to field although solar radiation was only 61% of ambient. Reduction to 195 ppmv [CO2] reduced agdw to 56±5% (SE, increase to 780 ppmv increased agdw to 128±8%, and 1560 ppmv increased agdw to 142±5%. In 2013WS, crop ET was measured by weighing the water extracted daily from the chambers by the air conditioners controlling air humidity. Chamber ETo was calculated according to FAO and empirically corrected via observed pan evaporation in chamber vs. field. For 390 ppmv [CO2], Kc was about 1 during crop establishment but increased to about 3 at flowering. 195 ppmv CO2 reduced Kc, 780 ppmv increased it, but at 1560 ppmv it declined. Whole-season crop water use was 564 mm (195 ppmv, 719 mm (390 ppmv, 928 mm (780 ppmv and 803 mm (1560 ppmv. With increasing [CO2], crop water use efficiency (WUE gradually increased from 1.59 g kg-1 (195 ppmv to 2.88 g kg-1 (1560 ppmv. Transpiration efficiency (TE measured on flag leaves responded more strongly to [CO2] than WUE. Responses of some morphological traits are also reported. In conclusion, increased CO2 promotes biomass more than water use of irrigated rice, causing increased WUE, but it does not help saving water. Comparability

  6. An algorithm for variational data assimilation of contact concentration measurements for atmospheric chemistry models

    Science.gov (United States)

    Penenko, Alexey; Penenko, Vladimir

    2014-05-01

    Contact concentration measurement data assimilation problem is considered for convection-diffusion-reaction models originating from the atmospheric chemistry study. High dimensionality of models imposes strict requirements on the computational efficiency of the algorithms. Data assimilation is carried out within the variation approach on a single time step of the approximated model. A control function is introduced into the source term of the model to provide flexibility for data assimilation. This function is evaluated as the minimum of the target functional that connects its norm to a misfit between measured and model-simulated data. In the case mathematical model acts as a natural Tikhonov regularizer for the ill-posed measurement data inversion problem. This provides flow-dependent and physically-plausible structure of the resulting analysis and reduces a need to calculate model error covariance matrices that are sought within conventional approach to data assimilation. The advantage comes at the cost of the adjoint problem solution. This issue is solved within the frameworks of splitting-based realization of the basic convection-diffusion-reaction model. The model is split with respect to physical processes and spatial variables. A contact measurement data is assimilated on each one-dimensional convection-diffusion splitting stage. In this case a computationally-efficient direct scheme for both direct and adjoint problem solution can be constructed based on the matrix sweep method. Data assimilation (or regularization) parameter that regulates ratio between model and data in the resulting analysis is obtained with Morozov discrepancy principle. For the proper performance the algorithm takes measurement noise estimation. In the case of Gaussian errors the probability that the used Chi-squared-based estimate is the upper one acts as the assimilation parameter. A solution obtained can be used as the initial guess for data assimilation algorithms that assimilate

  7. How to oxidize atmospheric CH4? - A challenge for the future

    International Nuclear Information System (INIS)

    Chazelas, Bruno; Leger, Alain; Ollivier, Marc

    2006-01-01

    Methane is an active Greenhouse effect gas whose concentration will likely increase in the future. The possible destabilisation of CH 4 clathrates (hydrates) due to anthropogenic climate warming, and the resulting outgasing of methane, could lead to a major increase of the global Greenhouse effect, with dramatic consequences for Humanity. For these reasons, the study of possible countermeasures should be actively considered. Here, we suggest taking advantage of the thermodynamic instability of CH 4 in air, and search for ways to oxidize it

  8. Comparison of atmosphere/aquatic environment concentration ratio of volatile chlorinated hydrocarbons between temperate regions and Antarctica.

    Science.gov (United States)

    Zoccolillo, Lelio; Amendola, Luca; Insogna, Susanna

    2009-09-01

    For the purpose of understanding the transport and deposition mechanisms and the air-water distribution of some volatile chlorinated hydrocarbons (VCHCs), their atmosphere/aquatic environment concentration ratio was evaluated. In addition, for the purpose of differentiating VCHC behaviour in a temperate climate from its behaviour in a polar climate, the atmosphere/aquatic environment concentration ratio evaluated in matrices from temperate zones was compared with the concentration ratio evaluated in Antarctic matrices. In order to perform air samplings also at rigid Antarctic temperatures, the sampling apparatus, consisting of a diaphragm pump and canisters, was suitably modified. Chloroform, 1,1,1-trichloroethane, tetrachloromethane, 1,1,2-trichloroethylene and tetrachloroethylene were measured in air, water and snow using specific techniques composed of a purpose-made cryofocusing-trap-injector (for air samples) and a modified purge-and-trap injector (for aqueous samples) coupled to a gas chromatograph with mass spectrometric detection operating in selected ion monitoring mode. The VCHCs were retrieved in all the investigated matrices, both Italian and Antarctic, with concentrations varying from tens to thousands of ng m(-3) in air and from digits to hundreds of ng kg(-1) in water and snow. The atmosphere/aquatic environment concentration ratios were always found to be lower than 1. In particular, the Italian air/water concentration ratios were smaller than the Antarctic ones, by reason of the higher atmospheric photochemical activity in temperate zones. On the other hand, the Antarctic air/snow concentration ratios proved to be largely in favour of snow with respect to the Italian ratios, thus corroborating the hypothesis of a more efficient VCHC deposition mechanism and accumulation on Antarctic snow.

  9. Temperature dependence of carbon kinetic isotope effect for the oxidation reaction of ethane by OH radicals under atmospherically relevant conditions

    Science.gov (United States)

    Piansawan, Tammarat; Saccon, Marina; Laumer, Werner; Gensch, Iulia; Kiendler-Scharr, Astrid

    2015-04-01

    Modeling of the global distribution of atmospheric ethane sources and sinks by using the 13C isotopic composition requires accurate knowledge of the carbon kinetic isotope effect (KIE) of its atmospheric removal reactions. The quantum mechanical prediction implies the necessity to elucidate the temperature dependence of KIE within atmospherically relevant temperature range by experiment. In this study, the KIE and its temperature dependence for ethane oxidation by OH radicals was investigated at ambient pressure in a temperature range of 243 K to 303 K. The chemical reactions were carried out in a 15 L PFE reaction chamber, suspended in a thermally controlled oven. The isotope ratios of the gas phase components during the course of the reactions were measured by Thermal Desorption -- Gas Chromatography -- Isotope Ratio Mass Spectrometry (TD-GC-IRMS). For each temperature, the KIE was derived from the temporal evolution of the concentration and stable carbon isotope ratio (δ13C) of ethane using a method adapted from the relative reaction rate concept. The room temperature KIE of the ethane reaction with OH radicals was found to be 6.85 ± 0.32 ‰. This value is in agreement with the previously reported value of 8.57 ± 1.95 ‰ [Anderson et al. 2004] but has a substantially lower uncertainty. The experimental results will be discussed with the KIE temperature dependence predicted by quantum mechanical calculations. Reference: Rebecca S. Anderson, Lin Huang, Richard Iannone, Alexandra E. Thompson, and Jochen Rudolph (2004), Carbon Kinetic Isotope Effects in the Gas Phase Reactions of Light Alkanes and Ethene with the OH Radical at 296 ± 4 K, J. Phys. Chem. A, 108, 11537--11544

  10. Oxygen concentrators performance with nitrous oxide at 50:50 volume

    Directory of Open Access Journals (Sweden)

    Jorge Ronaldo Moll

    2014-06-01

    Full Text Available Background and objectives: Few investigations have addressed the safety of oxygen from concentrators for use in anesthesia in association with nitrous oxide. This study evaluated the percent of oxygen from a concentrator in association with nitrous oxide in a semi-closed rebreathing circuit. Methods: Adult patients undergoing low risk surgery were randomly allocated into two groups, receiving a fresh gas flow of oxygen from concentrators (O293 or of oxygen from concentrators and nitrous oxide (O293N2O. The fraction of inspired oxygen and the percentage of oxygen from fresh gas flow were measured every 10 min. The ratio of FiO2/oxygen concentration delivered was compared at various time intervals and between the groups. Results: Thirty patients were studied in each group. There was no difference in oxygen from concentrators over time for both groups, but there was a significant improvement in the FiO2 (p < 0.001 for O293 group while a significant decline (p < 0.001 for O293N2O. The FiO2/oxygen ratio varied in both groups, reaching a plateau in the O293 group. Pulse oximetry did not fall below 98.5% in either group. Conclusion: The FiO2 in the mixture of O293 and nitrous oxide fell during the observation period although oxygen saturation was higher than 98.5% throughout the study. Concentrators can be considered a stable source of oxygen for use during short anesthetic procedures, either pure or in association with nitrous oxide at 50:50 volume.

  11. The influence of oxygen concentration on the combustion of a fuel/oxidizer mixture

    Energy Technology Data Exchange (ETDEWEB)

    Biteau, H. [School of Engineering and Electronics, BRE Centre for Fire Safety Engineering, The University of Edinburgh, Edinburgh EH9 3JL (United Kingdom); Institut National de l' Environnement Industriel et des Risques, Parc Technologique Alata, Verneuil en Halatte (France); Fuentes, A. [Institut Universitaire des Systemes Thermiques Industriels (CNRS UMR 6595), Universite de Provence, 13453 Marseille Cedex 13 (France); Marlair, G. [Institut National de l' Environnement Industriel et des Risques, Parc Technologique Alata, Verneuil en Halatte (France); Torero, J.L. [School of Engineering and Electronics, BRE Centre for Fire Safety Engineering, The University of Edinburgh, Edinburgh EH9 3JL (United Kingdom)

    2010-04-15

    The aim of the present study is to investigate the influence of the O{sub 2} concentration on the combustion behaviour of a fuel/oxidizer mixture. The material tested is a ternary mixture of lactose, starch, and potassium nitrate, which has already been used in an attempt to estimate heat release rate using the FM-Global Fire Propagation Apparatus. It provides a well-controlled combustion chamber to study the evolution of the combustion products when varying the O{sub 2} concentration, between air and low oxidizer conditions. Different chemical behaviours have been exhibited. When the O{sub 2} concentration was reduced beyond 18%, large variations were observed in the CO{sub 2} and CO concentrations. This critical O{sub 2} concentration seems to be the limit before which the material only uses its own oxidizer to react. On the other hand, mass loss did not highlight this change in chemical reactions and remained similar whatever the test conditions. This presumes that the oxidation of CO into CO{sub 2} are due to reactions occurring in the gas phase especially for large O{sub 2} concentrations. This actual behaviour can be verified using a simplified flammability limit model adapted for the current work. Finally, a sensitivity analysis has been carried out to underline the influence of CO concentration in the evaluation of heat release rate using typical calorimetric methods. The results of this study provide a critical basis for the investigation of the combustion of a fuel/oxidizer mixture and for the validation of future numerical models. (author)

  12. Uncertain Henry's law constants compromise equilibrium partitioning calculations of atmospheric oxidation products

    Directory of Open Access Journals (Sweden)

    C. Wang

    2017-06-01

    Full Text Available Gas–particle partitioning governs the distribution, removal, and transport of organic compounds in the atmosphere and the formation of secondary organic aerosol (SOA. The large variety of atmospheric species and their wide range of properties make predicting this partitioning equilibrium challenging. Here we expand on earlier work and predict gas–organic and gas–aqueous phase partitioning coefficients for 3414 atmospherically relevant molecules using COSMOtherm, SPARC Performs Automated Reasoning in Chemistry (SPARC, and poly-parameter linear free-energy relationships. The Master Chemical Mechanism generated the structures by oxidizing primary emitted volatile organic compounds. Predictions for gas–organic phase partitioning coefficients (KWIOM/G by different methods are on average within 1 order of magnitude of each other, irrespective of the numbers of functional groups, except for predictions by COSMOtherm and SPARC for compounds with more than three functional groups, which have a slightly higher discrepancy. Discrepancies between predictions of gas–aqueous partitioning (KW/G are much larger and increase with the number of functional groups in the molecule. In particular, COSMOtherm often predicts much lower KW/G for highly functionalized compounds than the other methods. While the quantum-chemistry-based COSMOtherm accounts for the influence of intra-molecular interactions on conformation, highly functionalized molecules likely fall outside of the applicability domain of the other techniques, which at least in part rely on empirical data for calibration. Further analysis suggests that atmospheric phase distribution calculations are sensitive to the partitioning coefficient estimation method, in particular to the estimated value of KW/G. The large uncertainty in KW/G predictions for highly functionalized organic compounds needs to be resolved to improve the quantitative treatment of SOA formation.

  13. Snowpack-atmosphere gas exchanges of carbon dioxide, ozone, and nitrogen oxides at a hardwood forest site in northern Michigan

    Directory of Open Access Journals (Sweden)

    Brian Seok

    2015-03-01

    Full Text Available Abstract Snowpack-atmosphere gas exchanges of CO2, O3, and NOx (NO + NO2 were investigated at the University of Michigan Biological Station (UMBS, a mid-latitude, low elevation hardwood forest site, during the 2007–2008 winter season. An automated trace gas sampling system was used to determine trace gas concentrations in the snowpack at multiple depths continuously throughout the snow-covered period from two adjacent plots. One natural plot and one with the soil covered by a Tedlar sheet were setup for investigating whether the primary source of measured trace gases was biogenic (i.e., from the soil or non-biogenic (i.e., from the snowpack. The results were compared with the “White on Green” study conducted at the Niwot Ridge (NWT Long Term Ecological Research site in Colorado. The average winter CO2 flux ± s.e. from the soil at UMBS was 0.54 ± 0.037 µmol m-2 s-1 using the gradient diffusion method and 0.71 ± 0.012 µmol m-2 s-1 using the eddy covariance method, and in a similar range as found for NWT. Observed snowpack-O3 exchange was also similar to NWT. However, nitrogen oxides (NOx fluxes from snow at UMBS were 10 times smaller than those at NWT, and fluxes were bi-directional with the direction of the flux dependent on NOx concentrations in ambient air. The compensation point for the change in the direction of NOx flux was estimated to be 0.92 nmol mol-1. NOx in snow also showed diurnal dependency on incident radiation. These NOx dynamics in the snow at UMBS were notably different compared to NWT, and primarily determined by snow-atmosphere interactions rather than by soil NOx emissions.

  14. Low mercury concentration produces vasoconstriction, decreases nitric oxide bioavailability and increases oxidative stress in rat conductance artery.

    Directory of Open Access Journals (Sweden)

    Núbia Belem Lemos

    Full Text Available Mercury is an environmental pollutant that reduces nitric oxide (NO bioavailability and increases oxidative stress, having a close link with cardiovascular diseases, as carotid atherosclerosis, myocardial infarction, coronary heart disease and hypertension. One of the main sites affected by oxidative stress, which develops atherosclerosis, is the aorta. Under acute exposure to low mercury concentrations reactive oxygen species (ROS production were only reported for resistance vessels but if low concentrations of mercury also affect conductance arteries it is still unclear. We investigated the acute effects of 6 nM HgCl(2 on endothelial function of aortic rings measuring the reactivity to phenylephrine in rings incubated, or not, with HgCl(2 for 45 min, the protein expression for cyclooxygenase 2 (COX-2 and the AT1 receptor. HgCl(2 increased Rmax and pD2 to phenylephrine without changing the vasorelaxation induced by acetylcholine and sodium nitroprusside. Endothelial damage abolished the increased reactivity to phenylephrine. The increase of Rmax and pD2 produced by L-NAME was smaller in the presence of HgCl(2. Enalapril, losartan, indomethacin, furegrelate, the selective COX-2 inhibitor NS 398, superoxide dismutase and the NADPH oxidase inhibitor apocynin reverted HgCl(2 effects on the reactivity to phenylephrine, COX-2 protein expression was increased, and AT1 expression reduced. At low concentration, below the reference values, HgCl(2 increased vasoconstrictor activity by reducing NO bioavailability due to increased ROS production by NADPH oxidase activity. Results suggest that this is due to local release of angiotensin II and prostanoid vasoconstrictors. Results also suggest that acute low concentration mercury exposure, occurring time to time could induce vascular injury due to endothelial oxidative stress and contributing to increase peripheral resistance, being a high risk factor for public health.

  15. Germination of fungal conidia after exposure to low concentration ozone atmospheres.

    Science.gov (United States)

    The germinability of conidia of Alternaria alternata, Aspergillus flavus, Aspergillus niger, Penicillium digitatum, Penicillium expansum, or Penicillium italicum was determined periodically during exposure for approximately 100 days to a humid atmosphere of air alone or air containing 150 ppb ozone ...

  16. Case study of stratospheric ozone affecting ground-level oxidant concentrations

    International Nuclear Information System (INIS)

    Lamb, R.G.

    1977-01-01

    During the predawn hours of 19 November 1972, the air pollution monitoring station at Santa Rosa, Calif., recorded five consecutive hours of oxidant concentrations in excess of the present National Ambient Air Quality Standard. The highest of the hourly averages was 0.23 ppm. From a detailed analysis of the meteorological conditions surrounding this incident, it is shown that the ozone responsible for the anomalous concentrations originated in the stratosphere and not from anthropogenic sources

  17. Detection of atmospheric tritium by scintillation. Variations in its concentration in France; Detection du tritium atmospherique par scintillation. Evolution de sa concentration en France

    Energy Technology Data Exchange (ETDEWEB)

    Bibron, R [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1964-06-01

    The tritium released into the atmosphere as a result of the explosion of thermonuclear devices is a useful radioactive tracer for the study of certain geophysical problems. The low concentrations found however call for the use of extremely sensitive detectors. Two detection methods using liquid scintillators are described. In the first method, the sample is introduced into the scintillator in liquid form, after prior concentration of the tritium by electrolysis. In the second method the tritium is incorporated into the scintillator solvent molecule by chemical synthesis. In the last part of the report are examined the variations in the tritium concentration in rain-water and of the free hydrogen in the air in France. A discussion is then made of the seasonal variations in the case of rain-water and these are compared to the variations in the strontium-90 concentrations. (author) [French] Le tritium introduit dans l'atmosphere par les explosions d'armes thermonucleaires est un traceur radioactif Interessant pour l'etude de certains problemes de geophysique. Les faibles concentrations rencontrees obligent toutefois a utiliser des detecteurs extremement sensibles. On decrit deux methodes de detection utilisant des scintillateurs liquides. Dans la premiere methode, l'echantillon est introduit dans le scintillateur, sous forme aqueuse, apres une concentration prealable du tritium par electrolyse. Dans la seconde methode, le tritium est incorpore a la molecule du solvant du scintillateur par synthese chimique. Dans la derniere partie du rapport, on examine l'evolution de la concentration du tritium dans les eaux de precipitation et l'hydrogene libre de l'air en France. On discute ensuite les variations saisonnieres dans le cas des eaux de precipitation et on les compare aux variations du strontium 90. (auteur)

  18. Detection of atmospheric tritium by scintillation. Variations in its concentration in France; Detection du tritium atmospherique par scintillation. Evolution de sa concentration en France

    Energy Technology Data Exchange (ETDEWEB)

    Bibron, R. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1964-06-01

    The tritium released into the atmosphere as a result of the explosion of thermonuclear devices is a useful radioactive tracer for the study of certain geophysical problems. The low concentrations found however call for the use of extremely sensitive detectors. Two detection methods using liquid scintillators are described. In the first method, the sample is introduced into the scintillator in liquid form, after prior concentration of the tritium by electrolysis. In the second method the tritium is incorporated into the scintillator solvent molecule by chemical synthesis. In the last part of the report are examined the variations in the tritium concentration in rain-water and of the free hydrogen in the air in France. A discussion is then made of the seasonal variations in the case of rain-water and these are compared to the variations in the strontium-90 concentrations. (author) [French] Le tritium introduit dans l'atmosphere par les explosions d'armes thermonucleaires est un traceur radioactif Interessant pour l'etude de certains problemes de geophysique. Les faibles concentrations rencontrees obligent toutefois a utiliser des detecteurs extremement sensibles. On decrit deux methodes de detection utilisant des scintillateurs liquides. Dans la premiere methode, l'echantillon est introduit dans le scintillateur, sous forme aqueuse, apres une concentration prealable du tritium par electrolyse. Dans la seconde methode, le tritium est incorpore a la molecule du solvant du scintillateur par synthese chimique. Dans la derniere partie du rapport, on examine l'evolution de la concentration du tritium dans les eaux de precipitation et l'hydrogene libre de l'air en France. On discute ensuite les variations saisonnieres dans le cas des eaux de precipitation et on les compare aux variations du strontium 90. (auteur)

  19. Preparation of ammonium sulfate, calcium oxide and rare earth concentrate from phospho-gypsum

    International Nuclear Information System (INIS)

    Andrianov, A.M.; Rusin, N.F.; Dejneka, G.F.; Zinchenko, T.A.; Burova, T.I.

    1978-01-01

    A technological scheme is proposed which gives ammonium sulfate, purified (from admixtures of silicon, iron, titanium, aluminium) calcium oxide with direct yield of calcium 91% and rare-earth concentrate, containing 5.6% of Ln 2 O 3 with direct yield of 99.5%

  20. NITRATE AND NITROUS OXIDE CONCENTRATIONS IN SMALL STREAMS OF THE GEORGIA PIEDMONT

    Science.gov (United States)

    We are measuring dissolved nitrate and nitrous oxide concentrations and related parameters in 17 headwater streams in the South Fork Broad River, Georgia watershed on a monthly basis. The selected small streams drain watersheds dominated by forest, pasture, residential, or mixed...

  1. Continuous culture enrichments of ammonia-oxidizing bacteria at low ammonium concentrations

    NARCIS (Netherlands)

    Bollmann, A.; Laanbroek, H.J.

    2001-01-01

    Until now enrichments of ammonia-oxidizing bacteria from natural ammonium-limited environments have been performed mainly in the presence of much higher ammonia concentrations than those present in the natural environment and many have resulted in the enrichment and isolation of environmentally less

  2. Continuous culture enrichments of ammonia-oxidizing bacteria at low ammonium concentrations

    NARCIS (Netherlands)

    Bollmann, A.; Laanbroek, H.J.

    2001-01-01

    Until now enrichments of ammonia-oxidizing bacteria from natural ammonium-limited environments have been performed mainly in the presence of much higher ammonia concentrations than those present in the natural environment and many have resulted in the enrichment and isolation of environmentally

  3. Variations in exhaled nitric oxide concentration after three types of dives

    NARCIS (Netherlands)

    van Ooij, Pieter-Jan; Houtkooper, Antoinette; van Hulst, Rob

    2010-01-01

    An increase in exhaled nitric oxide concentration (FENO) occurs during an exacerbation of chronic obstructive lung disease or other inflammatory processes of the airway. Raised FENO levels are also observed during normobaric, mild hyperoxic exposures, whereas after hyperbaric hyperoxic exposure the

  4. To Error Problem Concerning Measuring Concentration of Carbon Oxide by Thermo-Chemical Sen

    Directory of Open Access Journals (Sweden)

    V. I. Nazarov

    2007-01-01

    Full Text Available The paper gives additional errors in respect of measuring concentration of carbon oxide by thermo-chemical sensors. A number of analytical expressions for calculation of error data and corrections for environmental factor deviations from admissible ones have been obtained in the paper

  5. Oxidation of Gas-Phase SO2 on the Surfaces of Acidic Microdroplets: Implications for Sulfate and Sulfate Radical Anion Formation in the Atmospheric Liquid Phase.

    Science.gov (United States)

    Hung, Hui-Ming; Hoffmann, Michael R

    2015-12-01

    The oxidation of SO2(g) on the interfacial layers of microdroplet surfaces was investigated using a spray-chamber reactor coupled to an electrospray ionization mass spectrometer. Four major ions, HSO3(-), SO3(•-), SO4(•-) and HSO4(-), were observed as the SO2(g)/N2(g) gas-mixture was passed through a suspended microdroplet flow, where the residence time in the dynamic reaction zone was limited to a few hundred microseconds. The relatively high signal intensities of SO3(•-), SO4(•-), and HSO4(-) compared to those of HSO3(-) as observed at pH SO2·H2O, which is also affected by the pH dependent uptake coefficient. When H2O2(g) was introduced into the spray chamber simultaneously with SO2(g), HSO3(-) is rapidly oxidized to form bisulfate in the pH range of 3 to 5. Conversion to sulfate was less at pH SO2(g) on the acidic microdroplets was estimated as 1.5 × 10(6) [S(IV)] (M s(-1)) at pH ≤ 3. In the presence of acidic aerosols, this oxidation rate is approximately 2 orders of magnitude higher than the rate of oxidation with H2O2(g) at a typical atmospheric H2O2(g) concentration of 1 ppb. This finding highlights the relative importance of the acidic surfaces for SO2 oxidation in the atmosphere. Surface chemical reactions on aquated aerosol surfaces, as observed in this study, are overlooked in most atmospheric chemistry models. These reaction pathways may contribute to the rapid production of sulfate aerosols that is often observed in regions impacted by acidic haze aerosol such as Beijing and other megacities around the world.

  6. Compostos carbonílicos atmosféricos: fontes, reatividade, níveis de concentração e efeitos toxicológicos Atmospheric carbonyl compounds: sources, reactivity, concentration levels and toxicologic effects

    Directory of Open Access Journals (Sweden)

    Marta Valéria Almeida Santana de Andrade

    2002-12-01

    Full Text Available In the last three decades carbonyl compounds, aldehydes and ketones, have received a great deal of attention due to their strong influence on photochemical smog formation and their recognized adverse human health effects. Carbonyl compounds are directly emitted into the atmosphere by combustion sources and also produced from photochemical oxidation of hydrocarbons and other organic compounds. In this paper it is presented a general overview about the carbonyl compounds sources, reactivity, concentration levels and toxicological effects.

  7. Use of liquid chromatography for measuring atmospheric sulfur dioxide and nitrogen oxide

    Energy Technology Data Exchange (ETDEWEB)

    Benova, E

    1973-02-01

    A literature search to ascertain the applicability of liquid chromatography to the analysis of atmospheric sulfur dioxide and various oxides of nitrogen is reported. Simple or enriched samples can be analyzed. Plastic bags are recommended for preparation of simple samples; and a table of 18 plastic materials, their manufacturers, and pollutants to which they are inert is provided. Enriched samples can be prepared in chromatographic columns by adsorption methods. Tables are provided listing carriers, stationary phase materials, temperatures, carrier liquids (helium or nitrogen), column dimensions, and other data recommended for chromatographic tests of SO/sub 2/ and NOx. Because of its reactivity and tendency to polymerize, sulfur trioxide should be reduced to SO/sub 2/ prior to analysis.

  8. Reliability and degradation of oxide VCSELs due to reaction to atmospheric water vapor

    Science.gov (United States)

    Dafinca, Alexandru; Weidberg, Anthony R.; McMahon, Steven J.; Grillo, Alexander A.; Farthouat, Philippe; Ziolkowski, Michael; Herrick, Robert W.

    2013-03-01

    850nm oxide-aperture VCSELs are susceptible to premature failure if operated while exposed to atmospheric water vapor, and not protected by hermetic packaging. The ATLAS detector in CERN's Large Hadron Collider (LHC) has had approximately 6000 channels of Parallel Optic VCSELs fielded under well-documented ambient conditions. Exact time-to-failure data has been collected on this large sample, providing for the first time actual failure data at use conditions. In addition, the same VCSELs were tested under a variety of accelerated conditions to allow us to construct a more accurate acceleration model. Failure analysis information will also be presented to show what we believe causes corrosion-related failure for such VCSELs.

  9. Atmospheric gaseous elemental mercury (GEM concentrations and mercury depositions at a high-altitude mountain peak in south China

    Directory of Open Access Journals (Sweden)

    X. W. Fu

    2010-03-01

    Full Text Available China is regarded as the largest contributor of mercury (Hg to the global atmospheric Hg budget. However, concentration levels and depositions of atmospheric Hg in China are poorly known. Continuous measurements of atmospheric gaseous elemental mercury (GEM were carried out from May 2008 to May 2009 at the summit of Mt. Leigong in south China. Simultaneously, deposition fluxes of THg and MeHg in precipitation, throughfall and litterfall were also studied. Atmospheric GEM concentrations averaged 2.80±1.51 ng m−3, which was highly elevated compared to global background values but much lower than semi-rural and industrial/urban areas in China. Sources identification indicates that both regional industrial emissions and long range transport of Hg from central, south and southwest China were corresponded to the elevated GEM level. Seasonal and diurnal variations of GEM were observed, which reflected variations in source intensity, deposition processes and meteorological factors. Precipitation and throughfall deposition fluxes of THg and MeHg in Mt. Leigong were comparable or lower compared to those reported in Europe and North America, whereas litterfall deposition fluxes of THg and MeHg were higher compared to Europe and North America. This highlights the importance of vegetation to Hg atmospheric cycling. In th remote forest ecosystem of China, deposition of GEM via uptake of foliage followed by litterfall was very important for the depletion of atmospheric Hg. Elevated GEM level in ambient air may accelerate the foliar uptake of Hg through air which may partly explain the elevated litterfall deposition fluxes of Hg observed in Mt. Leigong.

  10. Atmospheric cycles of nitrogen oxides and ammonia. [source strengths and destruction rates

    Science.gov (United States)

    Bottger, A.; Ehhalt, D. H.; Gravenhorst, G.

    1981-01-01

    The atmospheric cycles of nitrogenous trace compounds for the Northern and Southern Hemispheres are discussed. Source strengths and destruction rates for the nitrogen oxides: NO, NO2 and HNO3 -(NOX) and ammonia (NH3) are given as a function of latitude over continents and oceans. The global amounts of NOX-N and NH3-N produced annually in the period 1950 to 1975 (34 + 5 x one trillion g NOx-N/yr and 29 + or - 6 x one trillion g NH3-N/yr) are much less than previously assumed. Globally, natural and anthropogenic emissions are of similar magnitude. The NOx emission from anthropogenic sources is 1.5 times that from natural processes in the Northern Hemisphere, whereas in the Southern Hemisphere, it is a factor of 3 or 4 less. More than 80% of atmospheric ammonia seems to be derived from excrements of domestic animals, mostly by bulk deposition: 24 + or - 9 x one trillion g NO3 -N/yr and 21 + or - 9 x one trillion g NH4+-N/yr. Another fraction may be removed by absorption on vegetation and soils.

  11. Atmospheric fate of a series of carbonyl nitrates: photolysis frequencies and OH-oxidation rate constants.

    Science.gov (United States)

    Suarez-Bertoa, R; Picquet-Varrault, B; Tamas, W; Pangui, E; Doussin, J-F

    2012-11-20

    Multifunctional organic nitrates are potential NO(x) reservoirs whose atmospheric chemistry is somewhat little known. They could play an important role in the spatial distribution of reactive nitrogen species and consequently in ozone formation and distribution in remote areas. In this work, the rate constants for the reaction with OH radical and the photolysis frequencies of α-nitrooxyacetone, 3-nitrooxy-2-butanone, and 3-methyl-3-nitrooxy-2-butanone have been determined at room temperature at 1000 mbar total pressure of synthetic air. The rate constants for the OH oxidation were measured using the relative rate technique, with methanol as reference compound. The following rate constants were obtained for the reaction with OH: k(OH) = (6.7 ± 2.5) × 10(-13) cm(3) molecule(-1) s(-1) for α-nitrooxyacetone, (10.6 ± 4.1) × 10(-13) cm(3) molecule(-1) s(-1) for 3-nitrooxy-2-butanone, and (2.6 ± 0.9) × 10(-13) cm(3) molecule(-1) s(-1) for 3-methyl-3-nitrooxy-2-butanone. The corresponding photolysis frequencies extrapolated to typical atmospheric conditions for July first at noon at 40° latitude North were (4.8 ± 0.3) × 10(-5) s(-1), (5.7 ± 0.3) × 10(-5) s(-1), and (7.4 ± 0.2) × 10(-5) s(-1), respectively. The data show that photolysis is a major atmospheric sink for these organic nitrates.

  12. Understanding and Forecasting Upper Atmosphere Nitric Oxide Through Data Mining Analysis of TIMED/SABER Data

    Science.gov (United States)

    Flynn, S.; Knipp, D. J.; Matsuo, T.; Mlynczak, M. G.; Hunt, L. A.

    2017-12-01

    Storm time energy input to the upper atmosphere is countered by infrared radiative emissions from nitric oxide (NO). The temporal profile of these energy sources and losses strongly control thermospheric density profiles, which in turn affect the drag experienced by low Earth orbiting satellites. Storm time processes create NO. In some extreme cases an overabundance of NO emissions unexpectedly decreases atmospheric temperature and density to lower than pre-storm values. Quantifying the spatial and temporal variability of the NO emissions using eigenmodes will increase the understanding of how upper atmospheric NO behaves, and could be used to increase the accuracy of future space weather and climate models. Thirteen years of NO flux data, observed at 100-250 km altitude by the SABER instrument onboard the TIMED satellite, is decomposed into five empirical orthogonal functions (EOFs) and their amplitudes to: 1) determine the strongest modes of variability in the data set, and 2) develop a compact model of NO flux. The first five EOFs account for 85% of the variability in the data, and their uncertainty is verified using cross-validation analysis. Although these linearly independent EOFs are not necessarily independent in a geophysical sense, the first three EOFs correlate strongly with different geophysical processes. The first EOF correlates strongly with Kp and F10.7, suggesting that geomagnetic storms and solar weather account for a large portion of NO flux variability. EOF 2 shows annual variations, and EOF 3 correlates with solar wind parameters. Using these relations, an empirical model of the EOF amplitudes can be derived, which could be used as a predictive tool for future NO emissions. We illustrate the NO model, highlight some of the hemispheric asymmetries, and discuss the geophysical associations of the EOFs.

  13. The atmospheric impacts of monoterpene ozonolysis on global stabilised Criegee intermediate budgets and SO2 oxidation: experiment, theory and modelling

    Directory of Open Access Journals (Sweden)

    M. J. Newland

    2018-05-01

    Full Text Available The gas-phase reaction of alkenes with ozone is known to produce stabilised Criegee intermediates (SCIs. These biradical/zwitterionic species have the potential to act as atmospheric oxidants for trace pollutants such as SO2, enhancing the formation of sulfate aerosol with impacts on air quality and health, radiative transfer and climate. However, the importance of this chemistry is uncertain as a consequence of limited understanding of the abundance and atmospheric fate of SCIs. In this work we apply experimental, theoretical and numerical modelling methods to quantify the atmospheric impacts, abundance and fate of the structurally diverse SCIs derived from the ozonolysis of monoterpenes, the second most abundant group of unsaturated hydrocarbons in the atmosphere. We have investigated the removal of SO2 by SCIs formed from the ozonolysis of three atmospherically important monoterpenes (α-pinene, β-pinene and limonene in the presence of varying amounts of water vapour in large-scale simulation chamber experiments that are representative of boundary layer conditions. The SO2 removal displays a clear dependence on water vapour concentration, but this dependence is not linear across the range of [H2O] explored. At low [H2O] a strong dependence of SO2 removal on [H2O] is observed, while at higher [H2O] this dependence becomes much weaker. This is interpreted as being caused by the production of a variety of structurally (and hence chemically different SCIs in each of the systems studied, which displayed different rates of reaction with water and of unimolecular rearrangement or decomposition. The determined rate constants, k(SCI+H2O, for those SCIs that react primarily with H2O range from 4 to 310  ×  10−15 cm3 s−1. For those SCIs that predominantly react unimolecularly, determined rates range from 130 to 240 s−1. These values are in line with previous results for the (analogous stereo-specific SCI system of syn-/anti-CH3

  14. The atmospheric impacts of monoterpene ozonolysis on global stabilised Criegee intermediate budgets and SO2 oxidation: experiment, theory and modelling

    Science.gov (United States)

    Newland, Mike J.; Rickard, Andrew R.; Sherwen, Tomás; Evans, Mathew J.; Vereecken, Luc; Muñoz, Amalia; Ródenas, Milagros; Bloss, William J.

    2018-05-01

    The gas-phase reaction of alkenes with ozone is known to produce stabilised Criegee intermediates (SCIs). These biradical/zwitterionic species have the potential to act as atmospheric oxidants for trace pollutants such as SO2, enhancing the formation of sulfate aerosol with impacts on air quality and health, radiative transfer and climate. However, the importance of this chemistry is uncertain as a consequence of limited understanding of the abundance and atmospheric fate of SCIs. In this work we apply experimental, theoretical and numerical modelling methods to quantify the atmospheric impacts, abundance and fate of the structurally diverse SCIs derived from the ozonolysis of monoterpenes, the second most abundant group of unsaturated hydrocarbons in the atmosphere. We have investigated the removal of SO2 by SCIs formed from the ozonolysis of three atmospherically important monoterpenes (α-pinene, β-pinene and limonene) in the presence of varying amounts of water vapour in large-scale simulation chamber experiments that are representative of boundary layer conditions. The SO2 removal displays a clear dependence on water vapour concentration, but this dependence is not linear across the range of [H2O] explored. At low [H2O] a strong dependence of SO2 removal on [H2O] is observed, while at higher [H2O] this dependence becomes much weaker. This is interpreted as being caused by the production of a variety of structurally (and hence chemically) different SCIs in each of the systems studied, which displayed different rates of reaction with water and of unimolecular rearrangement or decomposition. The determined rate constants, k(SCI+H2O), for those SCIs that react primarily with H2O range from 4 to 310 × 10-15 cm3 s-1. For those SCIs that predominantly react unimolecularly, determined rates range from 130 to 240 s-1. These values are in line with previous results for the (analogous) stereo-specific SCI system of syn-/anti-CH3CHOO. The experimental results are

  15. Atmospheric concentrations of persistent organic pollutants over the Pacific Ocean near southern Taiwan and the northern Philippines.

    Science.gov (United States)

    Chao, How-Ran; Lin, Ding-Yan; Chen, Kuang-Yu; Gou, Yan-Yu; Chiou, Tsyr-Huei; Lee, Wen-Jhy; Chen, Shui-Jen; Wang, Lin-Chi

    2014-09-01

    This study investigates the atmospheric occurrence of persistent organic pollutants (POPs) over the Pacific Ocean near southern Taiwan and the northern Philippines. We determined sixty-six compounds, including polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), dioxin-like polychlorinated biphenyls (DLPCBs), polybrominated diphenyl ethers (PBDEs), as well as polychlorinated diphenyl ethers (PCDEs), polybrominated dibenzo-p-dioxins and dibenzofurans (PBDD/Fs), and polybrominated biphenyls (PBBs), in air samples simultaneously collected from the offshore oceanic atmosphere (n=6) and over a rural area (n=2). We calculated the atmospheric World Health Organization 2005 toxic equivalency levels (WHO2005-TEQ), for the total dioxin-like POPs, including PCDD/Fs, DLPCBs, and PBDD/Fs, being 0.00612 pg WHO2005-TEQ/m(3) and 0.0138 pg WHO2005-TEQ/m(3) over the ocean and land, respectively. We found unexpected lower averaged atmospheric PBDE concentrations in the rural area (15.9 pg/m(3)) than over the ocean (31.1 pg/m(3)) due to higher levels of the BDE209 congener, although the difference was not statistically significant. We have compared and reported our field results with previously published datasets over the global oceans, which suggest PCBs and PBDEs are the dominant chemical contaminants in the global oceanic atmosphere among these halogenated POPs (e.g. PCBs and Σdi-hepta PBDEs could be found in the range of 0.09-48.7 and 8.07-94.0 pg/m(3), respectively, including our dataset). However, there are still very few investigations on the global atmospheric levels of PBDD/Fs, PCDEs and PBBs and our data sums to these earlier studies. Finally, we point out that the halogenated POPs originated from Taiwan or the continental East Asia which could easily reach remote ocean sites via atmospheric transport. Copyright © 2014 Elsevier B.V. All rights reserved.

  16. HTO and OBT activity concentrations in soil at the historical atmospheric HT release site (Chalk River Laboratories)

    International Nuclear Information System (INIS)

    Kim, S.B.; Bredlaw, M.; Korolevych, V.Y.

    2012-01-01

    Tritium is routinely released by the Chalk River Laboratories (CRL) nuclear facilities. Three International HT release experiments have been conducted at the CRL site in the past. The site has not been disturbed since the last historical atmospheric testing in 1994 and presents an opportunity to assess the retention of tritium in soil. This study is devoted to the measurement of HTO and OBT activity concentration profiles in the subsurface 25 cm of soil. In terms of soil HTO, there is no evidence from the past HT release experiments that HTO was retained. The HTO activity concentration in the soil pore water appears similar to concentrations found in background areas in Ontario. In contrast, OBT activity concentrations in soil at the same site were significantly higher than HTO activity concentrations in soil. Elevated OBT appears to reside in the top layer of the soil (0–5 cm). In addition, OBT activity concentrations in the top soil layer did not fluctuate much with season, again, quite in contrast with soil HTO. This result suggests that OBT activity concentrations retained the signature of the historical tritium releases. Highlights: ► At the historical HT release site, HTO and OBT activity concentrations in soil depths were investigated. ► Most organically bound tritium exists in the top layer of the soil. ► The results indicated that OBT activity concentrations can be reflective of historical tritium releases into the environment.

  17. The impact of Southwest Airline's contribution to atmospheric Carbon Dioxide and Nitrous Oxide totals

    Science.gov (United States)

    Wilkerson, Cody L.

    Over the last century, aviation has grown to become an economical juggernaut. The industry creates innovation, connects people, and maintains a safety goal unlike any other field. However, as the world becomes more populated with technology and individuals, a general curiosity as to how human activity effects the planet is becoming of greater interest. This study presents what one domestic airline in the United States, Southwest Airlines, contributes to the atmospheric make-up of the planet. Utilizing various sources of quantifiable data, an outcome was reached that shows the amount of Carbon Dioxide and Nitrous Oxide produced by Southwest Airlines from 2002 to 2013. This topic was chosen due to the fact that there are no real quantifiable values of emission statistics from airlines available to the public. Further investigation allowed for Southwest Airlines to be compared to the overall Carbon Dioxide and Nitrous Oxide contributions of the United States for the year 2011. The results showed that with the absence of any set standard on emissions, it is vital that one should be established. The data showed that the current ICAO standard emission values showed a higher level of emissions than when Southwest Airline's fleet was analyzed using their actual fleet mix.

  18. Ball lightning from atmospheric discharges via metal nanosphere oxidation: from soils, wood or metals.

    Science.gov (United States)

    Abrahamson, John

    2002-01-15

    The slow (diffusion-limited) oxidation of metal nanoparticles has previously been proposed as the mechanism for ball lightning energy release, and argued to be the result of a normal lightning strike on soil. Here this basic model of networked nanoparticles is detailed further, and extended to lightning strikes on metal structures, and also to the action of other storm-related discharges or man-made discharges. The basic model predicted the important properties of "average" observed ball lightning, and the extension in this paper also covers high-energy examples of ball lightning. Laboratory checks of the theory are described, and predictions given of what conditions are necessary for observing ball lightning in the laboratory. Key requirements of the model are a sheltered region near the strike foot and starting materials which can generate a metal vapour under intensive heating, including soil, wood or a metal structure. The evolution of hydrocarbons (often plastics) along with metal vapour can ensure the local survival of the metal vapour even in an oxidizing atmosphere. Subsequent condensation of this vapour to metallic nanoparticles in networks provides the coherence of a ball structure, which also releases light over an extended time. Also discussed is the passage of ball lightning through a sheet of building material, including glass, and its occasional charring of flesh on close contact.

  19. Oxidative modification and electrochemical inactivation of Escherichia coli upon cold atmospheric pressure plasma exposure.

    Directory of Open Access Journals (Sweden)

    Marlène Dezest

    Full Text Available Cold atmospheric pressure plasmas (CAPPs are known to have bactericidal effects but the mechanism of their interaction with microorganisms remains poorly understood. In this study the bacteria Escherichia coli were used as a model and were exposed to CAPPs. Different gas compositions, helium with or without adjunctions of nitrogen or oxygen, were used. Our results indicated that CAPP induced bacterial death at decontamination levels depend on the duration, post-treatment storage and the gas mixture composition used for the treatment. The plasma containing O2 in the feeding gas was the most aggressive and showed faster bactericidal effects. Structural modifications of treated bacteria were observed, especially significant was membrane leakage and morphological changes. Oxidative stress caused by plasma treatment led to significant damage of E. coli. Biochemical analyses of bacterial macromolecules indicated massive intracellular protein oxidation. However, reactive oxygen and nitrogen species (RONS are not the only actors involved in E. coli's death, electrical field and charged particles could play a significant role especially for He-O2 CAPP.

  20. Organic matter in uranium concentration during ancient bed oxidation of carboniferons sediments

    International Nuclear Information System (INIS)

    Kruglova, V.G.; Uspenskij, V.A.; Dement'ev, P.K.; Kochenov, A.V.

    1984-01-01

    Changes in the organic matter accompanying the process of epigenetic ore formation are studied using the example of a deposit localized in carboniferous molasse strata of the Cretaceous period. Peculiarities of the organic matter as the main mineralization agent are studied by a complex of physical and themical methods. A distinct relationship between the uranium concentration and the degree of organic matter oxigenation is a most characteristic feature of the ore localization, however, there is no direct correlation between the contents of uranium and organic matter in ores. Uranium minerallzation was accumulated during infiltration of acid uraniferous.waters into grey stratum in the process of the bed oxidation zone formation oxidizing. Brown coal matter possessing a maximum adsorbability, as compared to other sedimentary rocks, apprared to be the uranium precipitator. The adsorption was accompanie by the formation of proper uranium minerals (coffinite, pitchblende) due to uranium reduction by oxidizing organic matter. Thus, the oxidative epigenesis was an are-forming process with the uranium concentration on organic matter proportionally to oxidation of the latter

  1. Transcriptional Response of the Archaeal Ammonia Oxidizer Nitrosopumilus maritimus to Low and Environmentally Relevant Ammonia Concentrations

    Science.gov (United States)

    Stahl, David A.

    2013-01-01

    The ability of chemoautotrophic ammonia-oxidizing archaea to compete for ammonia among marine microorganisms at low ambient concentrations has been in part attributed to their extremely high affinity for ammonia, but as yet there is no mechanistic understanding of supporting metabolism. We examined transcription of selected genes for anabolic functions (CO2 fixation, ammonia transport, and cell wall synthesis) and a central catabolic function (ammonia oxidation) in the thaumarchaeon Nitrosopumilus maritimus SCM1 growing at two ammonia concentrations, as measured by combined ammonia and ammonium, one well above the Km for ammonia oxidation (∼500 μM) and the other well below the Km (ammonia-replete to ammonia-limiting conditions. Transcript levels for ammonia oxidation, CO2 fixation, and one of the ammonia transport genes were approximately the same at high and low ammonia availability. Transcripts for all analyzed genes decreased with time in the complete absence of ammonia, but with various rates of decay. The new steady-state mRNA levels established are presumably more reflective of the natural physiological state of ammonia-oxidizing archaea and offer a reference for interpreting message abundance patterns in the natural environment. PMID:23995944

  2. Size Resolved Mass Concentration and Elemental Composition of Atmospheric Aerosols over the Eastern Mediterranean Area

    Czech Academy of Sciences Publication Activity Database

    Smolík, Jiří; Ždímal, Vladimír; Schwarz, Jaroslav; Lazaridis, M.; Havránek, Vladimír; Eleftheriadis, K.; Mihalopoulos, N.; Bryant, C.; Colbeck, I.

    2003-01-01

    Roč. 3, - (2003), s. 2207-2216 ISSN 1680-7324 Grant - others:ENVK2(XE) 1999/00052 Institutional research plan: CEZ:AV0Z1048901; CEZ:AV0Z4072921 Keywords : atmospheric particles * elemental composition * PM1 Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.317, year: 2003

  3. Size Resolved Mass Concentration and Elemental Composition of Atmospheric Aerosols over the Eastern Mediterranean Area

    Czech Academy of Sciences Publication Activity Database

    Smolík, Jiří; Ždímal, Vladimír; Schwarz, Jaroslav; Lazaridis, M.; Havránek, Vladimír; Eleftheriadis, K.; Mihalopoulos, N.; Bryant, C.; Colbeck, I.

    2003-01-01

    Roč. 3, - (2003), s. 2547-2573 ISSN 1680-7367 Grant - others:ENVK2(XE) 1999/00052 Institutional research plan: CEZ:AV0Z1048901; CEZ:AV0Z4072921 Keywords : atmospheric particles * PM1 * elemental composition Subject RIV: CF - Physical ; Theoretical Chemistry

  4. Future Atmospheric CO2 Concentration and Environmental Consequences for the Feed Market: a Consequential LCA

    DEFF Research Database (Denmark)

    Saxe, Henrik; Hamelin, Lorie; Hinrichsen, Torben

    2014-01-01

    that such altered chemical composition and crop yields would have for the production of pig feed. Results revealed, among others, that an extra European demand of pig feed under an atmospheric [CO2] of 550 μmole mole-1 would lead to ca. 6% less expansion of additional arable land worldwide, in comparison to feed...

  5. Future atmospheric CO2 concentration and environmental consequences for the feed market: a consequential LCA

    DEFF Research Database (Denmark)

    Saxe, Henrik; Hamelin, Lorie; Hinrichsen, Torben

    2014-01-01

    that such altered chemical composition and crop yields would have for the production of pig feed. Results revealed, among others, that an extra European demand of pig feed under an atmospheric [CO2] of 550 μmole mole-1 would lead to ca. 6% less expansion of additional arable land worldwide, in comparison to feed...

  6. Particle concentration and flux dynamics in the atmospheric boundary layer as the indicator of formation mechanism

    DEFF Research Database (Denmark)

    Lauros, J.; Sogachev, Andrey; Smolander, S.

    2011-01-01

    the atmospheric boundary layer during nucleation event days shows a highly dynamical picture, where particle formation is coupled with chemistry and turbulent transport. We have demonstrated the suitability of our turbulent mixing scheme in reproducing the most important characteristics of particle dynamics...... within the boundary layer. Deposition and particle flux simulations show that deposition affects noticeably only the smallest particles...

  7. Inter-annual variability of the atmospheric carbon dioxide concentrations as simulated with global terrestrial biosphere models and an atmospheric transport model

    Energy Technology Data Exchange (ETDEWEB)

    Fujita, Daisuke; Saeki, Tazu; Nakazawa, Takakiyo [Tohoku Univ., Sendai (Japan). Center for Atmospheric and Oceanic Studies; Ishizawa, Misa; Maksyutov, Shamil [Inst. for Global Change Research, Yokohama (Japan). Frontier Research System for Global Change; Thornton, Peter E. [National Center for Atmospheric Research, Boulder, CO (United States). Climate and Global Dynamics Div.

    2003-04-01

    Seasonal and inter-annual variations of atmospheric CO{sub 2} for the period from 1961 to 1997 have been simulated using a global tracer transport model driven by a new version of the Biome BioGeochemical Cycle model (Biome-BGC). Biome-BGC was forced by daily temperature and precipitation from the NCEP reanalysis dataset, and the calculated monthly-averaged CO{sub 2} fluxes were used as input to the global transport model. Results from an inter-comparison with the Carnegie-Ames-Stanford Approach model (CASA) and the Simulation model of Carbon CYCLE in Land Ecosystems (Sim-CYCLE) model are also reported. The phase of the seasonal cycle in the Northern Hemisphere was reproduced generally well by Biome-BGC, although the amplitude was smaller compared to the observations and to the other biosphere models. The CO{sub 2} time series simulated by Biome-BGC were compared to the global CO{sub 2} concentration anomalies from the observations at Mauna Loa and the South Pole. The modeled concentration anomalies matched the phase of the inter-annual variations in the atmospheric CO{sub 2} observations; however, the modeled amplitude was lower than the observed value in several cases. The result suggests that a significant part of the inter-annual variability in the global carbon cycle can be accounted for by the terrestrial biosphere models. Simulations performed with another climate-based model, Sim-CYCLE, produced a larger amplitude of inter-annual variability in atmospheric CO{sub 2}, making the amplitude closer to the observed range, but with a more visible phase mismatch in a number of time periods. This may indicate the need to increase the Biome-BGC model sensitivity to seasonal and inter-annual changes in temperature and precipitation.

  8. Inter-annual variability of the atmospheric carbon dioxide concentrations as simulated with global terrestrial biosphere models and an atmospheric transport model

    International Nuclear Information System (INIS)

    Fujita, Daisuke; Saeki, Tazu; Nakazawa, Takakiyo; Ishizawa, Misa; Maksyutov, Shamil; Thornton, Peter E.

    2003-01-01

    Seasonal and inter-annual variations of atmospheric CO 2 for the period from 1961 to 1997 have been simulated using a global tracer transport model driven by a new version of the Biome BioGeochemical Cycle model (Biome-BGC). Biome-BGC was forced by daily temperature and precipitation from the NCEP reanalysis dataset, and the calculated monthly-averaged CO 2 fluxes were used as input to the global transport model. Results from an inter-comparison with the Carnegie-Ames-Stanford Approach model (CASA) and the Simulation model of Carbon CYCLE in Land Ecosystems (Sim-CYCLE) model are also reported. The phase of the seasonal cycle in the Northern Hemisphere was reproduced generally well by Biome-BGC, although the amplitude was smaller compared to the observations and to the other biosphere models. The CO 2 time series simulated by Biome-BGC were compared to the global CO 2 concentration anomalies from the observations at Mauna Loa and the South Pole. The modeled concentration anomalies matched the phase of the inter-annual variations in the atmospheric CO 2 observations; however, the modeled amplitude was lower than the observed value in several cases. The result suggests that a significant part of the inter-annual variability in the global carbon cycle can be accounted for by the terrestrial biosphere models. Simulations performed with another climate-based model, Sim-CYCLE, produced a larger amplitude of inter-annual variability in atmospheric CO 2 , making the amplitude closer to the observed range, but with a more visible phase mismatch in a number of time periods. This may indicate the need to increase the Biome-BGC model sensitivity to seasonal and inter-annual changes in temperature and precipitation

  9. Catalytic oxidation of concentrated orange oil phase by synthetic metallic complexes biomimetic to MMO enzyme.

    Science.gov (United States)

    Fernandes, Ilizandra A; Esmelindro, Maria Carolina; Corazza, Marcos L; Franceschi, Elton; Treichel, Helen; de Oliveira, Debora; Frizzo, Caren D; Oliveira, J Vladimir

    2010-07-01

    This paper reports the catalytic oxidation of the concentrated orange oil phase using the complexes [Fe(III)(BMPP)Cl(micro-O)Fe(III)Cl(3)], [Cu(II)(BTMEA)(2)Cl]Cl and [Co(II)(BMPP)]Cl(2) biomimetic to methane monooxygenase enzyme as catalysts and hydrogen peroxide as oxidant. The reaction products of oil oxidation, mainly nootkatone, were identified by gas chromatography/mass spectrometry. A screening of catalysts was performed through a full 2(3) experimental design, varying the temperature from 30 to 70 degrees C, the catalyst concentration from 7.0 x 10(-4) to 1.5 x 10(-3) mol L(-1) and the oxidant/substrate molar ratio from 1:1 to 3:1. The results of reaction kinetics employing the most promising catalysts showed that conversions to nootkatone of up to 8% were achieved after 16 h at 70 degrees C. The results obtained in this study in terms of nootkatone production should be considered encouraging, since a real, industrially collected, raw material, instead of pure valencene, was employed in the reaction experiments, with a final content about ten times that present in the original concentrated oil.

  10. Source, concentration, and distribution of elemental mercury in the atmosphere in Toronto, Canada

    International Nuclear Information System (INIS)

    Cairns, Elaine; Tharumakulasingam, Kavitharan; Athar, Makshoof; Yousaf, Muhammad; Cheng, Irene; Huang, Y.; Lu, Julia; Yap, Dave

    2011-01-01

    Atmospheric gaseous elemental mercury [GEM] at 1.8, 4, and 59 m above ground, in parking lots, and in indoor and outdoor air was measured in Toronto City, Canada from May 2008-July 2009. The average GEM value at 1.8 m was 1.89 ± 0.62 ng m -3 . The GEM values increased with elevation. The average GEM in underground parking lots ranged from 1.37 to 7.86 ng m -3 and was higher than those observed from the surface parking lots. The GEM in the indoor air ranged from 1.21 to 28.50 ng m -3 , was higher in the laboratories than in the offices, and was much higher than that in the outdoor air. All these indicate that buildings serve as sources of mercury to the urban atmosphere. More studies are needed to estimate the contribution of urban areas to the atmospheric mercury budget and the impact of indoor air on outdoor air quality and human health. - Highlights: → Buildings served as mercury sources to urban atmosphere. → Atmospheric mercury level increased with increasing height in the street canyon. → Emission from vehicles and ground surfaces was not the major sources of Hg to urban air. → Mercury levels were higher in indoor than outdoor air and in laboratories than in offices. → Mercury levels were higher in the outdoor air near building walls. - Buildings serve as sources of gaseous elemental mercury and research is needed to quantify the emission and to assess the impact of indoor air on outdoor air quality and human health.

  11. Impact of marine mercury cycling on coastal atmospheric mercury concentrations in the North- and Baltic Sea region

    Directory of Open Access Journals (Sweden)

    Johannes Bieser

    2016-06-01

    Full Text Available Abstract The cycling of mercury between ocean and atmosphere is an important part of the global Hg cycle. Here we study the regional contribution of the air-sea exchange in the North- and Baltic Sea region. We use a newly developed coupled regional chemistry transport modeling (CTM system to determine the flux between atmosphere and ocean based on the meteorological model COSMO-CLM, the ocean-ecosystem model ECOSMO, the atmospheric CTM CMAQ and a newly developed module for mercury partitioning and speciation in the ocean (MECOSMO. The model was evaluated using atmospheric observations of gaseous elemental mercury (GEM, surface concentrations of dissolved gaseous mercury (DGM, and air-sea flux (ASF calculations based on observations made on seven cruises in the western and central Baltic Sea and three cruises in the North Sea performed between 1991 and 2006. It was shown that the model is in good agreement with observations: DGM (Normalized Mean Bias NMB=-0.27 N=413, ASF (NMB=-0.32, N=413, GEM (NMB=0.07, N=2359. Generally, the model was able to reproduce the seasonal DGM cycle with the best agreement during winter and autumn (NMBWinter=-0.26, NMBSpring=-0.41, NMBSummer=-0.29, NMBAutumn=-0.03. The modelled mercury evasion from the Baltic Sea ranged from 3400 to 4000 kg/a for the simulation period 1994–2007 which is on the lower end of previous estimates. Modelled atmospheric deposition, river inflow and air-sea exchange lead to an annual net Hg accumulation in the Baltic Sea of 500 to 1000 kg/a. For the North Sea the model calculates an annual mercury flux into the atmosphere between 5700 and 6000 kg/a. The mercury flux from the ocean influenced coastal atmospheric mercury concentrations. Running CMAQ coupled with the ocean model lead to better agreement with GEM observations. Directly at the coast GEM concentrations could be increased by up to 10% on annual average and observed peaks could be reproduced much better. At stations 100km downwind

  12. Applications of Ground-based Mobile Atmospheric Monitoring: Real-time Characterization of Source Emissions and Ambient Concentrations

    Science.gov (United States)

    Goetz, J. Douglas

    Gas and particle phase atmospheric pollution are known to impact human and environmental health as well as contribute to climate forcing. While many atmospheric pollutants are regulated or controlled in the developed world uncertainty still remains regarding the impacts from under characterized emission sources, the interaction of anthropogenic and naturally occurring pollution, and the chemical and physical evolution of emissions in the atmosphere, among many other uncertainties. Because of the complexity of atmospheric pollution many types of monitoring have been implemented in the past, but none are capable of perfectly characterizing the atmosphere and each monitoring type has known benefits and disadvantages. Ground-based mobile monitoring with fast-response in-situ instrumentation has been used in the past for a number of applications that fill data gaps not possible with other types of atmospheric monitoring. In this work, ground-based mobile monitoring was implemented to quantify emissions from under characterized emission sources using both moving and portable applications, and used in a novel way for the characterization of ambient concentrations. In the Marcellus Shale region of Pennsylvania two mobile platforms were used to estimate emission rates from infrastructure associated with the production and transmission of natural gas using two unique methods. One campaign investigated emissions of aerosols, volatile organic compounds (VOCs), methane, carbon monoxide (CO), nitrogen dioxide (NO2), and carbon dioxide (CO 2) from natural gas wells, well development practices, and compressor stations using tracer release ratio methods and a developed fenceline tracer release correction factor. Another campaign investigated emissions of methane from Marcellus Shale gas wells and infrastructure associated with two large national transmission pipelines using the "Point Source Gaussian" method described in the EPA OTM-33a. During both campaigns ambient concentrations

  13. Methane oxidation and formation of EPS in compost: effect of oxygen concentration

    International Nuclear Information System (INIS)

    Wilshusen, J.H.; Hettiaratchi, J.P.A.; Visscher, A. de; Saint-Fort, R.

    2004-01-01

    Oxygen concentration plays an important role in the regulation of methane oxidation and the microbial ecology of methanotrophs. However, this effect is still poorly quantified in soil and compost ecosystems. The effect of oxygen on the formation of exopolymeric substances (EPS) is as yet unknown. We studied the effect of oxygen on the evolution of methanotrophic activity. At both high and low oxygen concentrations, peak activity was observed twice within a period of 6 months. Phospholipid fatty acid analysis showed that there was a shift from type I to type II methanotrophs during this period. At high oxygen concentration, EPS production was about 250% of the amount at low oxygen concentration. It is hypothesized that EPS serves as a carbon cycling mechanism for type I methanotrophs when inorganic nitrogen is limiting. Simultaneously, EPS stimulates nitrogenase activity in type II methanotrophs by creating oxygen-depleted zones. The kinetic results were incorporated in a simulation model for gas transport and methane oxidation in a passively aerated biofilter. Comparison between the model and experimental data showed that, besides acting as a micro-scale diffusion barrier, EPS can act as a barrier to macro-scale diffusion, reducing the performance of such biofilters. - 1.5% oxygen resulted in a slightly higher and more stable methane oxidation activity

  14. Rising atmospheric carbon dioxide concentration and the future of C4 crops for food and fuel

    OpenAIRE

    Leakey, Andrew D.B.

    2009-01-01

    Crops with the C4 photosynthetic pathway are vital to global food supply, particularly in the tropical regions where human well-being and agricultural productivity are most closely linked. While rising atmospheric [CO2] is the driving force behind the greater temperatures and water stress, which threaten to reduce future crop yields, it also has the potential to directly benefit crop physiology. The nature of C4 plant responses to elevated [CO2] has been controversial. Recent evidence from fr...

  15. Catalytic Oxidation of Benzophenone Hydrazone with Alumina-supported KMnO{sub 4} under Oxygen Atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Kang Hyeok; Ko, Kwang Youn [Ajou University, Suwon (Korea, Republic of)

    2006-02-15

    KMnO{sub 4}/alumina reagent, which is cheap and environmentally safe, can serve as a catalytic oxidant under O{sub 2} atmosphere for the oxidation of benzophenone hydrazone. To the best of our knowledge, the present works are the first example where KMnO{sub 4}/alumina reagent acts as a catalytic oxidant under O{sub 2} atmosphere. Diphenyldiazomethane (Ph{sub 2}CN{sub 2}) is widely used for the protection of carboxylic acids by conversion to their diphenylmethyl (dpm) esters since dpm group can be easily deprotected by mild acidic condition or hydrogenolysis, especially in the field of b-lactams and peptides. Diphenyldiazomethane has been prepared by the oxidation of benzophenone hydrazone with reagents such as active manganese dioxide, mercuric oxide, peracetic acid, iodosobenzene diacetate or OXONE. However, some methods suffer from a disadvantage such as toxic nature of reagent, strong oxidative conditions or incompatibility with certain functional groups. For example, OXONE may not be employed for the in situ protection of carboxylic acid containing sulfide group due to the possibility of the concomitant oxidation of sulfide group.

  16. The effect of the atmosphere on the optical properties of as-synthesized colloidal indium tin oxide

    International Nuclear Information System (INIS)

    Capozzi, Charles J; Joshi, Salil; Gerhardt, Rosario A; Ivanov, Ilia N

    2009-01-01

    The optical properties of indium tin oxide (ITO) have often been explored when it is in the form of deposited thin films. In this study, a colloidal chemistry approach is taken to investigate the influence of the atmosphere on the optical properties of ITO nanoparticles. X-ray diffraction (XRD), transmission electron microscopy (TEM), absorption spectroscopy and photoluminescence (PL) were used to characterize colloidal ITO samples, synthesized under aerated and inert conditions, with the same composition. In both cases, the ITO can be completely dispersed in a non-polar solvent without any evidence of agglomeration. For the ITO made in air, the nanoparticle-solvent solution exhibits a pale green color, and XRD and TEM indicate an average particle size of ∼7 nm and small shrinkage in the lattice structure. When the ITO is synthesized under inert conditions, the solution turns blue, and XRD and TEM indicate an average particle size of ∼8 nm and even less strain in the lattice than for the ITO synthesized under aerated conditions. The change in color and lattice strain is attributed to the difference in oxygen vacancy concentration for the ITO nanoparticles synthesized under aerated and inert conditions, which exhibit different optical band gap values of 3.89 eV and 4.05 eV, respectively. Our work here shows that thin film deposition or sintering steps may not be required for studying the optical properties of as-synthesized ITO nanoparticles.

  17. Impacts of Mercury Pollution Controls on Atmospheric Mercury Concentration and Occupational Mercury Exposure in a Hospital.

    Science.gov (United States)

    Li, Ping; Yang, Yan; Xiong, Wuyan

    2015-12-01

    Mercury (Hg) and Hg-containing products are used in a wide range of settings in hospitals. Hg pollution control measures were carried out in the pediatric ward of a hospital to decrease the possibility of Hg pollution occurring and to decrease occupational Hg exposure. Total gaseous Hg (TGM) concentrations in the pediatric ward and hair and urine Hg concentrations for the pediatric staff were determined before and after the Hg pollution control measures had been implemented. A questionnaire survey performed indicated that the pediatric staff had little understanding of Hg pollution and that appropriate disposal techniques were not always used after Hg leakage. TGM concentrations in the pediatric ward and urine Hg (UHg) concentrations for the pediatric staff were 25.7 and 22.2% lower, respectively, after the Hg pollution control measures had been implemented than before, which indicated that the control measures were effective. However, TGM concentrations in the pediatric ward remained significantly higher than background concentrations and UHg concentrations for the pediatric staff were remained significantly higher than the concentrations in control group, indicating continued existence of certain Hg pollution.

  18. Use of a Simple GIS-Based Model in Mapping the Atmospheric Concentration of γ-HCH in Europe

    Directory of Open Access Journals (Sweden)

    Pilar Vizcaino

    2014-10-01

    Full Text Available The state-of-the-art of atmospheric contaminant transport modeling provides accurate estimation of chemical concentrations. However, existing complex models, sophisticated in terms of process description and potentially highly accurate, may entail expensive setups and require very detailed input data. In contexts where detailed predictions are not needed (e.g., for regulatory risk assessment or life cycle impact assessment of chemicals, simple models allowing quick evaluation of contaminants may be preferable. The goal of this paper is to illustrate and critically discuss the use of a simple equation proposed by Pistocchi and Galmarini (2010, which can be implemented through basic GIS functions, to predict atmospheric concentrations of lindane (γ-HCH in Europe from both local and remote sources. Concentrations were computed for 1995 and 2005 assuming different modes of use of lindane and consequently different spatial patterns of emissions. Results were compared with those from the well-established MSCE-POP model (2005 developed within EMEP (European Monitoring and Evaluation Programme, and with available monitoring data, showing acceptable correspondence in terms of the orders of magnitude and spatial distribution of concentrations, especially when the background effect of emissions from extracontinental sources, estimated using the same equation, is added to European emissions.

  19. Effect of elevated atmospheric CO2 concentration on growth and leaf litter decomposition of Quercus acutissima and Fraxinus rhynchophylla.

    Directory of Open Access Journals (Sweden)

    Sangsub Cha

    Full Text Available The atmospheric carbon dioxide (CO2 level is expected to increase substantially, which may change the global climate and carbon dynamics in ecosystems. We examined the effects of an elevated atmospheric CO2 level on the growth of Quercus acutissima and Fraxinus rhynchophylla seedlings. We investigated changes in the chemical composition of leaf litter, as well as litter decomposition. Q. acutissima and F. rhynchophylla did not show differences in dry weight between ambient CO2 and enriched CO2 treatments, but they exhibited different patterns of carbon allocation, namely, lower shoot/root ratio (S/R and decreased specific leaf area (SLA under CO2-enriched conditions. The elevated CO2 concentration significantly reduced the nitrogen concentration in leaf litter while increasing lignin concentrations and carbon/nitrogen (C/N and lignin/N ratios. The microbial biomass associated with decomposing Q. acutissima leaf litter was suppressed in CO2 enrichment chambers, while that of F. rhynchophylla was not. The leaf litter of Q. acutissima from the CO2-enriched chambers, in contrast with F. rhynchophylla, contained much lower nutrient concentrations than that of the litter in the ambient air chambers. Consequently, poorer litter quality suppressed decomposition.

  20. Effect of elevated atmospheric CO2 concentration on growth and leaf litter decomposition of Quercus acutissima and Fraxinus rhynchophylla.

    Science.gov (United States)

    Cha, Sangsub; Chae, Hee-Myung; Lee, Sang-Hoon; Shim, Jae-Kuk

    2017-01-01

    The atmospheric carbon dioxide (CO2) level is expected to increase substantially, which may change the global climate and carbon dynamics in ecosystems. We examined the effects of an elevated atmospheric CO2 level on the growth of Quercus acutissima and Fraxinus rhynchophylla seedlings. We investigated changes in the chemical composition of leaf litter, as well as litter decomposition. Q. acutissima and F. rhynchophylla did not show differences in dry weight between ambient CO2 and enriched CO2 treatments, but they exhibited different patterns of carbon allocation, namely, lower shoot/root ratio (S/R) and decreased specific leaf area (SLA) under CO2-enriched conditions. The elevated CO2 concentration significantly reduced the nitrogen concentration in leaf litter while increasing lignin concentrations and carbon/nitrogen (C/N) and lignin/N ratios. The microbial biomass associated with decomposing Q. acutissima leaf litter was suppressed in CO2 enrichment chambers, while that of F. rhynchophylla was not. The leaf litter of Q. acutissima from the CO2-enriched chambers, in contrast with F. rhynchophylla, contained much lower nutrient concentrations than that of the litter in the ambient air chambers. Consequently, poorer litter quality suppressed decomposition.

  1. Ammonium and nitrite oxidation at nanomolar oxygen concentrations in oxygen minimum zone waters.

    Science.gov (United States)

    Bristow, Laura A; Dalsgaard, Tage; Tiano, Laura; Mills, Daniel B; Bertagnolli, Anthony D; Wright, Jody J; Hallam, Steven J; Ulloa, Osvaldo; Canfield, Donald E; Revsbech, Niels Peter; Thamdrup, Bo

    2016-09-20

    A major percentage of fixed nitrogen (N) loss in the oceans occurs within nitrite-rich oxygen minimum zones (OMZs) via denitrification and anammox. It remains unclear to what extent ammonium and nitrite oxidation co-occur, either supplying or competing for substrates involved in nitrogen loss in the OMZ core. Assessment of the oxygen (O2) sensitivity of these processes down to the O2 concentrations present in the OMZ core (Chile at manipulated O2 levels between 5 nmol⋅L(-1) and 20 μmol⋅L(-1) Rates of both processes were detectable in the low nanomolar range (5-33 nmol⋅L(-1) O2), but demonstrated a strong dependence on O2 concentrations with apparent half-saturation constants (Kms) of 333 ± 130 nmol⋅L(-1) O2 for ammonium oxidation and 778 ± 168 nmol⋅L(-1) O2 for nitrite oxidation assuming one-component Michaelis-Menten kinetics. Nitrite oxidation rates, however, were better described with a two-component Michaelis-Menten model, indicating a high-affinity component with a Km of just a few nanomolar. As the communities of ammonium and nitrite oxidizers were similar to other OMZs, these kinetics should apply across OMZ systems. The high O2 affinities imply that ammonium and nitrite oxidation can occur within the OMZ core whenever O2 is supplied, for example, by episodic intrusions. These processes therefore compete with anammox and denitrification for ammonium and nitrite, thereby exerting an important control over nitrogen loss.

  2. The IPAC-NC field campaign: a pollution and oxidization pool in the lower atmosphere over Huabei, China

    Directory of Open Access Journals (Sweden)

    J. Z. Ma

    2012-05-01

    Full Text Available In the past decades, regional air pollution characterized by photochemical smog and grey haze-fog has become a severe environmental problem in China. To investigate this, a field measurement campaign was performed in the Huabei region, located between 32–42° N latitude in eastern China, during the period 2 April–16 May 2006 as part of the project "Influence of Pollution on Aerosols and Cloud Microphysics in North China" (IPAC-NC. It appeared that strong pollution emissions from urban and industrial centers tend to accumulate in the lower atmosphere over the central area of Huabei. We observed widespread, very high SO2 mixing ratios, about 20–40 ppbv at 0.5–1.5 km altitude and 10–30 ppbv at 1.5–3.0 km altitude. Average CO mixing ratios were 0.65–0.7 ppmv at 0.5–1.5 km altitude, and very high CO around 1 ppmv was observed during some flights, and even higher levels at the surface. We find the high pollution concentrations to be associated with enhanced levels of OH and HO2 radicals, calculated with a chemical box model constrained by the measurements. In the upper part of the boundary layer and in the lower free troposphere, high CO and SO2 compete with relatively less NO2 in reacting with OH, being efficiently recycled through HO2, preventing a net loss of HOx radicals. In addition to reactive hydrocarbons and CO, the oxidation of SO2 causes significant ozone production over Huabei (up to ~13% or 2.0 ppbv h−1 at 0.8 km altitude. Our results indicate that the lower atmosphere over Huabei is not only strongly polluted but also acts as an oxidation pool, with pollutants undergoing very active photochemistry over this part of China.

  3. Application of a Chemiluminescence Detector for the Measurement of Total Oxides of Nitrogen and Ammonia in the Atmosphere

    Science.gov (United States)

    Hodgeson, J. A.; Bell, J. P.; Rehme, K. A.; Krost, K. J.; Stevens, R. K.

    1971-01-01

    By means of the thermal conversion of nitrogen dioxide to the nitric oxide, the chemiluminescent nitric oxide monitor, based on the nitric oxide plus ozone reaction, may be used for monitoring nitrogen dioxide plus nitric oxide (NO(x)). Under conditions previously described, ammonia is also converted to nitric oxide and therefore interferes. A metal surface, gold wool or stainless steel, operated at two different temperatures has been used to convert only nitrogen dioxide or nitrogen dioxide plus ammonia. Quantitative conversion of nitrogen dioxide to nitric oxide has been obtained at temperatures as low as 200 C. Conversion of ammonia is effected at temperatures of 300 C or higher. By the addition of a converter the basic nitric oxide monitor may be used for measuring NO(x) or NO(x) plus ammonia. As an alternate mode, for a fixed high temperature, a specific scrubber is described for removing NH3 without affecting NO2 concentrations.

  4. Short-term 222Rn activity concentration changes in underground spaces with limited air exchange with the atmosphere

    Science.gov (United States)

    Fijałkowska-Lichwa, L.; Przylibski, T. A.

    2011-04-01

    The authors investigated short-time changes in 222Rn activity concentration occurring yearly in two underground tourist facilities with limited air exchange with the atmosphere. One of them is Niedźwiedzia (Bear) Cave in Kletno, Poland - a natural space equipped with locks ensuring isolation from the atmosphere. The other site is Fluorite Adit in Kletno, a section of a disused uranium mine. This adit is equipped with a mechanical ventilation system, operated periodically outside the opening times (at night). Both sites are situated within the same metamorphic rock complex, at similar altitudes, about 2 km apart. The measurements conducted revealed spring and autumn occurrence of convective air movements. In Bear Cave, this process causes a reduction in 222Rn activity concentration in the daytime, i.e. when tourists, guides and other staff are present in the cave. From the point of view of radiation protection, this is the best situation. For the rest of the year, daily concentrations of 222Rn activity in the cave are very stable. In Fluorite Adit, on the other hand, significant variations in daily 222Rn activity concentrations are recorded almost all year round. These changes are determined by the periods of activity and inactivity of mechanical ventilation. Unfortunately this is inactive in the daytime, which results in the highest values of 222Rn activity concentration at the times when tourists and staff are present in the adit. Slightly lower concentrations of radon in Fluorite Adit are recorded in the winter season, when convective air movements carry a substantial amount of radon out into the atmosphere. The incorrect usage of mechanical ventilation in Fluorite Adit results in the most unfavourable conditions in terms of radiation protection. The staff working in that facility are exposed practically throughout the year to the highest 222Rn activity concentrations, both at work (in the adit) and at home (outside their working hours). Therefore, not very well

  5. Iron Oxide Minerals in Atmospheric Dust and Source Sediments-Studies of Types and Properties to Assess Environmental Effects

    Science.gov (United States)

    Reynolds, R. L.; Goldstein, H. L.; Moskowitz, B. M.; Till, J. L.; Flagg, C.; Kokaly, R. F.; Munson, S.; Landry, C.; Lawrence, C. R.; Hiza, M. M.; D'Odorico, P.; Painter, T. H.

    2011-12-01

    Ferric oxide minerals in atmospheric dust can influence atmospheric temperatures, accelerate melting of snow and ice, stimulate marine phytoplankton productivity, and impact human health. Such effects vary depending on iron mineral type, size, surface area, and solubility. Generally, the presence of ferric oxides in dust is seen in the red, orange, or yellow hues of plumes that originate in North Africa, central and southwest Asia, South America, western North America, and Australia. Despite their global importance, these minerals in source sediments, atmospheric dust, and downwind aeolian deposits remain poorly described with respect to specific mineralogy, particle size and surface area, or presence in far-traveled aerosol compounds. The types and properties of iron minerals in atmospheric dust can be better understood using techniques of rock magnetism (measurements at 5-300 K), Mössbauer and high-resolution visible and near-infrared reflectance spectroscopy; chemical reactivity of iron oxide phases; and electron microscopy for observing directly the ferric oxide coatings and particles. These studies can elucidate the diverse environmental effects of iron oxides in dust and can help to identify dust-source areas. Dust-source sediments from the North American Great Basin and Colorado Plateau deserts and the Kalahari Desert, southern Africa, were used to compare average reflectance values with a magnetic parameter (hard isothermal remanent magnetization, HIRM) for ferric oxide abundance. Lower reflectance values correspond strongly with higher HIRM values, indicating that ferric oxides (hematite or goethite, or both) contribute to absorption of solar radiation in these sediments. Dust deposited to snow cover of the San Juan Mountains (Colorado) and Wasatch Mountains (Utah) was used to characterize dust composition compared with properties of sediments exposed in source-areas identified from satellite retrievals. Results from multiple methods indicate that

  6. Sensing sulfur oxides and other sulfur bearing pollutants with solid electrolyte pellets. I. Gas concentration cells

    Energy Technology Data Exchange (ETDEWEB)

    Chamberland, A M; Gauthier, J M

    1977-01-01

    A new sensing technique using a solid electrolyte has been demonstrated for sulfur-bearing pollutants. Based on potentiometric measurements across a pellet of potassium sulfate, this sensor allows concentrations of sulfur dioxides, sulfur trioxide, hydrogen sulfide, methyl mercaptan and carbonyl sulfide in air to be measured with accuracy. Its operational concentration range at the present time is 0.1 ppM up to at least 10,000 ppM. The presence of other common pollutants such as carbon dioxide, methane, nitric oxide and nitrogen dioxide does not interfere with the measurement of air samples containing sulfur-bearing pollutants.

  7. Electrochemical oxidation of biological pretreated and membrane separated landfill leachate concentrates on boron doped diamond anode

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Bo, E-mail: 357436235@qq.com [School of Materials Science and Engineering, Central South University, Changsha 410083 (China); Yu, Zhiming, E-mail: zhiming@csu.edu.cn [School of Materials Science and Engineering, Central South University, Changsha 410083 (China); State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083 (China); Wei, Qiuping, E-mail: qiupwei@csu.edu.cn [School of Materials Science and Engineering, Central South University, Changsha 410083 (China); State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083 (China); Long, HangYu, E-mail: 55686385@qq.com [School of Materials Science and Engineering, Central South University, Changsha 410083 (China); Xie, Youneng, E-mail: 1187272844@qq.com [School of Materials Science and Engineering, Central South University, Changsha 410083 (China); Wang, Yijia, E-mail: 503630433@qq.com [School of Materials Science and Engineering, Central South University, Changsha 410083 (China)

    2016-07-30

    Highlights: • High quality boron-doped diamond film electrodes were synthesized on Nb substrates. • Electrochemical oxidation on boron-doped diamond anode is an effective method for treating landfill leachate concentrates. • Optimal operating conditions for electrochemical oxidation of landfill leachate concentrates is determined. • 87.5% COD removal and 74.06% NH{sub 3}−N removal were achieved after 6 h treatment. - Abstract: In the present study, the high quality boron-doped diamond (BDD) electrodes with excellent electrochemical properties were deposited on niobium (Nb) substrates by hot filament chemical vapor deposition (HFCVD) method. The electrochemical oxidation of landfill leachate concentrates from disc tube reverse osmosis (DTRO) process over a BDD anode was investigated. The effects of varying operating parameters, such as current density, initial pH, flow velocity and cathode material on degradation efficiency were also evaluated following changes in chemical oxygen demand (COD) and ammonium nitrogen (NH{sub 3}−N). The instantaneous current efficiency (ICE) was used to appraise different operating conditions. As a result, the best conditions obtained were as follows, current density 50 mA cm{sup −2}, pH 5.16, flow velocity 6 L h{sup −1}. Under these conditions, 87.5% COD and 74.06% NH{sub 3}−N removal were achieved after 6 h treatment, with specific energy consumption of 223.2 kWh m{sup −3}. In short, these results indicated that the electrochemical oxidation with BDD/Nb anode is an effective method for the treatment of landfill leachate concentrates.

  8. Do lagoons near concentrated animal feeding operations promote nitrous oxide supersaturation?

    International Nuclear Information System (INIS)

    Makris, Konstantinos C.; Sarkar, Dibyendu; Andra, Syam S.; Bach, Stephan B.H.; Datta, Rupali

    2009-01-01

    Animal wastewater lagoons nearby concentrated animal feeding operations (CAFOs) represent the latest tendency in global animal farming, severely impacting the magnitude of greenhouse gas emissions, including nitrous oxide (N 2 O). We hypothesized that lagoon wastewater could be supersaturated with N 2 O as part of incomplete microbial nitrification/denitrification processes, thereby regulating the N 2 O partitioning in the gaseous phase. The objectives of this study were: (i) to investigate the magnitude of dissolved N 2 O concentrations in the lagoon; and (ii) to determine the extent to which supersaturation of N 2 O occurs in wastewater lagoons. Dissolved N 2 O concentrations in the wastewater samples were high, ranging from 0.4 to 40.5 μg N 2 O mL -1 . Calculated dissolved N 2 O concentrations from the experimentally measured partition coefficients were much greater than those typically expected in aquatic systems ( 2 O mL -1 ). Knowledge of the factors controlling the magnitude of N 2 O supersaturation could potentially bridge mass balance differences between in situ measurements and global N 2 O models. - Supersaturation of nitrous oxide may occur in lagoons near concentrated animal feeding operations.

  9. Development of metal oxide gas sensors for very low concentration (ppb) of BTEX vapors

    Science.gov (United States)

    Favard, A.; Aguir, K.; Contaret, T.; Caris, L.; Bendahan, M.

    2017-12-01

    The control and analysis of air quality have become a major preoccupation of the last twenty years. In 2008, the European Union has introduced a Directive (2008/50/EC) to impose measurement obligations and thresholds to not exceed for some pollutants, including BTEX gases, in view of their adverse effects on the health. In this paper, we show the ability to detect very low concentrations of BTEX using a gas microsensor based on metal oxide thin-film. A test bench able to generate very low vapors concentrations has been achieved and fully automated. Thin metal oxides layers have been realized by reactive magnetron sputtering. The sensitive layers are functionalized with gold nanoparticles by thermal evaporation technique. Our sensors have been tested on a wide range of concentrations of BTEX (5 - 500 ppb) and have been able to detect concentrations of a few ppb for operating temperatures below 593 K. These results are very promising for detection of very low BTEX concentration for indoor as well as outdoor application. We showed that the addition of gold nanoparticles on the sensitive layers decreases the sensors operating temperature and increases the response to BTEX gas. The best results are obtained with a sensitive layer based on ZnO.

  10. Record high peaks in PCB concentrations in the Arctic atmosphere due to long-range transport of biomass burning emissions

    Directory of Open Access Journals (Sweden)

    S. Eckhardt

    2007-08-01

    Full Text Available Soils and forests in the boreal region of the Northern Hemisphere are recognised as having a large capacity for storing air-borne Persistent Organic Pollutants (POPs, such as the polychlorinated biphenyls (PCBs. Following reductions of primary emissions of various legacy POPs, there is an increasing interest and debate about the relative importance of secondary re-emissions on the atmospheric levels of POPs. In spring of 2006, biomass burning emissions from agricultural fires in Eastern Europe were transported to the Zeppelin station on Svalbard, where record-high levels of many air pollutants were recorded (Stohl et al., 2007. Here we report on the extremely high concentrations of PCBs that were also measured during this period. 21 out of 32 PCB congeners were enhanced by more than two standard deviations above the long-term mean concentrations. In July 2004, about 5.8 million hectare of boreal forest burned in North America, emitting a pollution plume which reached the Zeppelin station after a travel time of 3–4 weeks (Stohl et al., 2006. Again, 12 PCB congeners were elevated above the long-term mean by more than two standard deviations, with the less chlorinated congeners being most strongly affected. We propose that these abnormally high concentrations were caused by biomass burning emissions. Based on enhancement ratios with carbon monoxide and known emissions factors for this species, we estimate that 130 and 66 μg PCBs were released per kilogram dry matter burned, respectively. To our knowledge, this is the first study relating atmospheric PCB enhancements with biomass burning. The strong effects on observed concentrations far away from the sources, suggest that biomass burning is an important source of PCBs for the atmosphere.

  11. A new procedure for estimating the cell temperature of a high concentrator photovoltaic grid connected system based on atmospheric parameters

    International Nuclear Information System (INIS)

    Fernández, Eduardo F.; Almonacid, Florencia

    2015-01-01

    Highlights: • Concentrating grid-connected systems are working at maximum power point. • The operating cell temperature is inherently lower than at open circuit. • Two novel methods for estimating the cell temperature are proposed. • Both predict the operating cell temperature from atmospheric parameters. • Experimental results show that both methods perform effectively. - Abstract: The working cell temperature of high concentrator photovoltaic systems is a crucial parameter when analysing their performance and reliability. At the same time, due to the special features of this technology, the direct measurement of the cell temperature is very complex and is usually obtained by using different indirect methods. High concentrator photovoltaic modules in a system are operating at maximum power since they are connected to an inverter. So that, their cell temperature is lower than the cell temperature of a module at open-circuit voltage since an important part of the light power density is converted into electricity. In this paper, a procedure for indirectly estimating the cell temperature of a high concentrator photovoltaic system from atmospheric parameters is addressed. Therefore, this new procedure has the advantage that is valid for estimating the cell temperature of a system at any location of interest if the atmospheric parameters are available. To achieve this goal, two different methods are proposed: one based on simple mathematical relationships and another based on artificial intelligent techniques. Results show that both methods predicts the cell temperature of a module connected to an inverter with a low margin of error with a normalised root mean square error lower or equal than 3.3%, an absolute root mean square error lower or equal than 2 °C, a mean absolute error lower or equal then 1.5 °C, and a mean bias error and a mean relative error almost equal to 0%

  12. Electron transport investigation of layered MoO3 oxides doped with different concentrations of Nb2O5 oxide

    International Nuclear Information System (INIS)

    Al-Khawaja, S.; Kasem, M.

    2008-07-01

    The dc and ac electric conductivity has been studied for numerous samples of molybdenum oxide MoO 3 doped with niobium oxide Nb 2 O 5 elaborated via the solid state reactions. By means of the electric resistivity and dielectricity curves obtained as a function of temperature, and according to the dopant concentration, the behaviour of these compounds has been allocated. Most of the investigated samples, which are insulating at room temperature, have been witnessed to exhibit simultaneously two different electric comportments; metallic and semiconducting within the range of low and high temperatures respectively, designated by a critical temperature related to the nature of the material. Both of these behaviours are attributed electronically to ionic conduction mechanism, occurring in the solid material formed upon doping with Nb 2 O 5 , which is utterly diffused into the layered structure of MoO 3 particularly for x≥40% concentrations and accompanied by relaxation in the dielectric function between 5 Hz and 13 M Hz.(Authors)

  13. Influence of some atmospheric variables on the concentration and particle size distribution of sulfate in urban air

    Energy Technology Data Exchange (ETDEWEB)

    Wagman, J; Lee, Jr, R E; Axt, C J

    1967-01-01

    Variations in the particle size distribution and concentration of atmospheric sulfate during a week in each of four cities were assessed with regard to the influence of such factors as location, humidity, sulfur dioxide level and time of day. Average sulfate mass median equivalent diameters (MMD) in Cincinnati, Chicago and Fairfax (Ohio) were nearly the same (0.42 micron) despite large differences in sulfate concentration and heterodispersity. A higher MMD (0.66 micron) in downtown Philadelphia was at least partly attributable to the presence of dust generated by road construction near the sampling site. Sulfate MMD generally increased with increasing relative humidity, whereas sulfate concentration was more closely correlated with absolute humidity except when SO/sub 2/ levels exceeded 3pphm. Periodic variations in the sulfate parameters at the different locations were characterized by the lack of a consistent pattern and could not be explained on the basis of humidity changes alone.

  14. Recent changes in the oxidized to reduced nitrogen ratio in atmospheric precipitation

    Science.gov (United States)

    Kurzyca, Iwona; Frankowski, Marcin

    2017-10-01

    In this study, the characteristics of precipitation in terms of various nitrogen forms (NO3-, NO2-, NH4+, Norganic, Ntotal) is presented. The samples were collected in the areas of different anthropogenic pressure (urban area vs. ecologically protected woodland area, ∼30 km distant from each other; Wielkopolska region, Poland). Based on the Nox and Nred emission profiles (Nox/Nred ratio), temporal and spatial comparison was carried out. For both sites, during a decade of observation, more than 60% of samples had higher contribution of N-NH4+ than N-NO3-, the amount of N-NO2- was negligible, and organic nitrogen amounted to 30% of total nitrogen content which varied up to 16 mg/l. The precipitation events w ith high concentration of nitrogen species were investigated in terms of possible local and remote sources of nitrogen (synoptic meteorology), to indicate the areas which can act as potential sources of N-compounds. Based on the chemometric analysis, it was found that Nred implies Nox and vice versa, due to interactions between them in the atmosphere. Taking into account the analysis of precipitation occurring simultaneously in both locations (about 50% of all rainfall episodes), it was observed that such factor as anthropogenic pressure differentiates but does not determine the chemical composition of precipitation in the investigated areas (urban vs. woodland area; distance of ∼30 km). Thermodynamics of the atmosphere had a significant impact on concentrations of N-NO3- and N-NH4+ in precipitation, as well as the circulation of air masses and remote N sources responsible for transboundary inflow of pollutants.

  15. Determination of optimal conditions for pressure oxidative leaching of Sarcheshmeh Molybdenite concentrate using Taguchi method

    Directory of Open Access Journals (Sweden)

    Khoshnevisana A.

    2012-01-01

    Full Text Available The present research work is based on finding the optimum conditions for pressure oxidative leaching of the molybdenite concentrate to produce technical-grade molybdic oxide (MoO3 with high recovery through further treatment of the filtrate solution. The Taguchi method was used to design and minimize the number of experiments. By using Taguchi orthogonal (L25 array, five parameters (time, temperature, oxygen pressure, pulp density and acid concentration at five levels were selected for 25 experiments. The experiments were designed and carried out in a high-pressure reactor in the presence of nitric acid as solvent and oxidizing agent for the molybdenite concentrate and its ReS2 content. The optimum conditions for pressure leaching of molybdenite were obtained through using Signal to Noise analysis and modified by using Minitab software prediction tool. Furthermore, the optimum condition for an economical pressure leaching of rhenium sulfide (ReS2 was achieved with the same process. Analysis of variance (ANOVA showed that the pulp density is of paramount importance in this process.

  16. Geomagnetic control of mesospheric nitric oxide concentration from simultaneous D and F region ionization measurements

    International Nuclear Information System (INIS)

    Pradhan, S.N.; Shirke, J.S.

    1978-01-01

    Investigations are made of D-region electron density profiles derived from 'partial reflection' measurements over a low latitude station (Ahmedabad) during a year of low solar activity. The index relating the electron density with the solar zenith angle is found to increase towards lower zenith angles suggesting both diurnal and seasonal variations in the Nitric oxide concentration. A close correlation is also found between the electron density at 80 km and the maximum ionization density in the F region above. This is interpreted as due to concomitant variation of a sizeable fraction of the Nitric oxide concentration in the mesosphere and lower thermosphere with the overhead F region ionization. A simplified global model is presented for the mesospheric Nitric oxide concentration based on the morphological features of F region and the relationship existing between the ionization levels in F and D regions. Many observed features of the D region ionization including the solar zenith angle dependence, latitudinal and geomagnetic anomaly and long term variability are explained on the basis of this model

  17. Oxidation of PCEA nuclear graphite by low water concentrations in helium

    Energy Technology Data Exchange (ETDEWEB)

    Contescu, Cristian I., E-mail: ContescuCI@ornl.gov [Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831-6087 (United States); Mee, Robert W. [Department of Business Analytics and Statistics, University of Tennessee, Knoxville, TN 37996-0525 (United States); Wang, Peng [Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831-6087 (United States); Romanova, Anna V.; Burchell, Timothy D. [Department of Business Analytics and Statistics, University of Tennessee, Knoxville, TN 37996-0525 (United States)

    2014-10-15

    Accelerated oxidation tests were performed to determine kinetic parameters of the chronic oxidation reaction (i.e. slow, continuous, and persistent) of PCEA graphite in contact with helium coolant containing low moisture concentrations in high temperature gas-cooled reactors. To the authors’ knowledge such a study has not been done since the detailed analysis of reaction of H-451 graphite with steam (Velasquez, Hightower, Burnette, 1978). Since that H-451 graphite is now unavailable, it is urgently needed to characterize chronic oxidation behavior of new graphite grades that are being considered for use in gas-cooled reactors. The Langmuir–Hinshelwood mechanism of carbon oxidation by water results in a non-linear reaction rate expression, with at least six different parameters. They were determined in accelerated oxidation experiments that covered a large range of temperatures (800–1100 °C), and partial pressures of water (15–850 Pa) and hydrogen (30–150 Pa) and used graphite specimens thin enough (4 mm) in order to avoid diffusion effects. Data analysis employed a statistical method based on multiple likelihood estimation of parameters and simultaneous fitting of non-linear equations. The results show significant material-specific differences between graphite grades PCEA and H-451 which were attributed to microstructural dissimilarity between the two materials. It is concluded that kinetic data cannot be transferred from one graphite grade to another.

  18. Non-OH Chemistry in Oxidation Flow Reactors for the Study of Atmospheric Chemistry Systematically Examined by Modeling

    Science.gov (United States)

    Peng, Zhe; Day, Douglas A.; Ortega, Amber M.; Palm, Brett B.; Hu, Weiwei; Stark, Harald; Li, Rui; Tsigaridis, Kostas; Brune, William H.; Jimenez, Jose L.

    2016-01-01

    Oxidation flow reactors (OFRs) using low-pressure Hg lamp emission at 185 and 254 nm produce OH radicals efficiently and are widely used in atmospheric chemistry and other fields. However, knowledge of detailed OFR chemistry is limited, allowing speculation in the literature about whether some non-OH reactants, including several not relevant for tropospheric chemistry, may play an important role in these OFRs. These non-OH reactants are UV radiation, O(1D), O(3P), and O3. In this study, we investigate the relative importance of other reactants to OH for the fate of reactant species in OFR under a wide range of conditions via box modeling. The relative importance of non-OH species is less sensitive to UV light intensity than to relative humidity (RH) and external OH reactivity (OHRext), as both non-OH reactants and OH scale roughly proportional to UV intensity. We show that for field studies in forested regions and also the urban area of Los Angeles, reactants of atmospheric interest are predominantly consumed by OH. We find that O(1D), O(3P), and O3 have relative contributions to VOC consumption that are similar or lower than in the troposphere. The impact of O atoms can be neglected under most conditions in both OFR and troposphere. Under pathological OFR conditions of low RH and/or high OHRext, the importance of non-OH reactants is enhanced because OH is suppressed. Some biogenics can have substantial destructions by O3, and photolysis at non-tropospheric wavelengths (185 and 254 nm) may also play a significant role in the degradation of some aromatics under pathological conditions. Working under low O2 with the OFR185 mode allows OH to completely dominate over O3 reactions even for the biogenic species most reactive with O3. Non-tropospheric VOC photolysis may have been a problem in some laboratory and source studies, but can be avoided or lessened in future studies by diluting source emissions and working at lower precursor concentrations in lab studies, and by

  19. Influence of atmospheric stability and transport on CH{sub 4} concentrations in northern Spain

    Energy Technology Data Exchange (ETDEWEB)

    García, M. Ángeles, E-mail: magperez@fa1.uva.es; Sánchez, M. Luisa; Pérez, Isidro A.; Ozores, Marta I.; Pardo, Nuria

    2016-04-15

    Continuous methane (CH{sub 4}) concentrations were measured in Northern Spain over two years (2011–2012) by multi-point sampling at 1.8, 3.7 and 8.3 m using a Picarro analyser. The technique is based on cavity ring-down spectroscopy. The contrast in mean concentrations was about 1.2 ppb, with 95th percentiles differing by 2.2 ppb and mean minimum concentrations proving similar. Temporal variations of CH{sub 4} were also analysed, with a similar seasonal variability being found for the three heights. The highest CH{sub 4} concentrations were obtained in late autumn and winter and the lowest in summer, yielding a range of 52 ppb. This variation may depend on the active photochemical reaction with OH radical during a period of intense solar radiation and changes in soil conditions together with variations in emissions. Peak concentration levels were recorded at night-time, between 5:00–7:00 GMT, with mean values ranging between 1920 and 1923 ppb. The lowest value, around 1884 ppb, was obtained at 16:00 GMT. This diurnal variation was mainly related to vertical mixing and photochemistry. Therefore, CH{sub 4} concentrations were also examined using the bulk Richardson number (R{sub B}) as a stability indicator. Four groups were distinguished: unstable cases, situations with pure shear flow, transitional stages and drainage flows. The highest contrast in mean CH{sub 4} concentrations between lower and upper heights was obtained for the transition and drainage cases, mainly associated to high concentrations from nearby sources. The impact of long range transport was analysed by means of 3-day isobaric backward air mass trajectories, which were calculated taking into account origins from Europe, Africa, the Atlantic Ocean and Local conditions. Assessment of the results showed the influence of S and SE wind sectors, especially with Local conditions associated with low winds. Finally, an estimation of the background CH{sub 4} concentration in the study period provided an

  20. Variability of atmospheric krypton-85 activity concentrations observed close to the ITCZ in the southern hemisphere.

    Science.gov (United States)

    Bollhöfer, A; Schlosser, C; Ross, J O; Sartorius, H; Schmid, S

    2014-01-01

    Krypton-85 activity concentrations in surface air have been measured at Darwin, which is located in northern Australia and is influenced by seasonal monsoonal activity. Measurements between August 2007 and May 2010 covered three wet seasons. The mean activity concentration of krypton-85 measured during this period was 1.31±0.02Bqm(-3). A linear model fitted to the average monthly data, using month and monsoon as predictors, shows that krypton-85 activity concentration measured during the sampling period has declined by 0.01Bqm(-3) per year. Although there is no statistically significant difference in mean activity concentration of krypton-85 between wet and dry season, the model implies that activity concentration is higher by about 0.015Bqm(-3) during months influenced by the monsoon when a north westerly flow prevails. Backward dispersion runs using the Lagrangian particle dispersion model Hysplit4 highlight possible source regions during an active monsoon located deep in the northern hemisphere, and include reprocessing facilities in Japan and India. However, the contribution of these facilities to krypton-85 activity concentrations in Darwin would be less than 0.003Bqm(-3). Crown Copyright © 2013. Published by Elsevier Ltd. All rights reserved.

  1. Determination of atmospheric SO/sub 2/ concentrations that are dangerous to plant life

    Energy Technology Data Exchange (ETDEWEB)

    Stratmann, H

    1963-01-01

    Controlled climate experiments indicate that the reaction of plants is not simply proportional to the project of SO/sub 2/ concentration and exposure time, and the degree of damage inflicted increases in proportion to this product as the concentration itself increases. A determining factor is the fact that plants, even when kept in a controlled climate, undergo a diurnal cycle of sensitivity. High concentrations for a shorter time do more damage than low concentrations for a longer exposure time, indicating the existence of concentration peaks. Although most cultivated plants are resistant to night exposure, a night exposure immediately following a daylight exposure causes a multiplication of damages, as does a succession of peak concentrations. It has also been discovered that plants whose leaves are not fully developed suffer a higher degree of SO damage than those whose leaves are fully matured. In the case of deciduous trees, sensitivity increases in proportion to the development of the leaves, until full leaf maturity is reached. Older trees are more resistant to SO/sub 2/.

  2. Optimization of a model of red blood cells for the study of anti-oxidant drugs, in terms of concentration of oxidant and phosphate buffer.

    Science.gov (United States)

    Bureau, A; Lahet, J-J; Lenfant, F; Bouyer, F; Petitjean, M; Chaillot, B; Freysz, M

    2005-08-01

    The aggression of erythrocytes by an oxidative stress induces hemolysis. This paper aims to valid a model of erythrocytes in terms of composition of the phosphate buffer solution and of concentration of a well-known oxidant, AAPH. Three compositions of phosphate buffer solution are mixed with three concentrations of oxidant. The influence of these two parameters on hemolysis is independently studied by a variance analysis and a Kruskal-Wallis test when ANOVA is not available. The hemolysis rate increases with time at fixed oxidant concentration, but is not influenced by the composition of the buffer solution. The highest hemolysis rate, 90%, was only measured within 2 h with the highest oxidant concentration. If we retain this concentration of oxidant, the lower concentration of the buffer can by eliminated by a significant less hemolysis and the highest concentration of the buffer can by chosen in regard of the better precision for a similar hemolysis compared to the mean buffer. We hope to study the effect of anti-oxidant agent with such a model of erythrocytes.

  3. Responses of Metabolites in Soybean Shoot Apices to Changing Atmospheric Carbon Dioxide Concentrations

    Directory of Open Access Journals (Sweden)

    Richard Sicher

    2012-01-01

    Full Text Available Soybean seedlings were grown in controlled environment chambers with CO2 partial pressures of 38 (ambient and 72 (elevated Pa. Five or six shoot apices were harvested from individual 21- to 24-day-old plants. Metabolites were analyzed by gas chromatography and, out of 21 compounds, only sucrose and fructose increased in response to CO2 enrichment. One unidentified metabolite, Unk-21.03 decreased up to 80% in soybean apices in response to elevated CO2. Levels of Unk-21.03 decreased progressively when atmospheric CO2 partial pressures were increased from 26 to 100 Pa. Reciprocal transfer experiments showed that Unk-21.03, and sucrose in soybean apices were altered slowly over several days to changes in atmospheric CO2 partial pressures. The mass spectrum of Unk-21.03 indicated that this compound likely contained both an amino and carboxyl group and was structurally related to serine and aspartate. Our findings suggested that CO2 enrichment altered a small number of specific metabolites in soybean apices. This could be an important step in understanding how plant growth and development are affected by carbon dioxide enrichment.

  4. New instruments and methods for measuring the concentration of radioactive products in the atmosphere; Appareils recents et methodes nouvelles pour la mesure de la concentration des produits radioactifs dans l'atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Jehanno, C; Blanc, A; Lallemant, C; Roux, G [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1959-07-01

    Different recorders for radioactive aerosols have been developed for measuring the pollution of the atmosphere in laboratories or the external atmosphere. EAR 600. - Allows continuous measurement, instantaneously and 3 to 10 hours after sampling, of concentrations of {alpha} or {beta} emitting aerosols varying between some 10{sup -11} and some 10{sup -8} curie per cubic metre of air. EAR 800. - Allows continuous measurement of concentration of {alpha} emitting aerosols varying between 10{sup -11} and 10{sup -5} curie per cubic metre of air and concentration of {beta} emitting aerosols from 10{sup -11} to 10{sup -1} curie per cubic metre of air. EAR Plutonium. - Allows detection after several minutes of 1000 MPD (2 x 10{sup -9} curie par cubic metre), and after 8 hours 1 MPD (2 x 10{sup -12} curie per cubic metre). Two methods are used to separate the activity due to plutonium from that due to the descendants of radon and thoron: a) by amplitude discrimination, b) by RaC-RaC' and ThC-ThC' ({alpha} {beta} ) coincidences. SP4. This system, mounted on a jeep, allows the measurement of irradiation produced on the ground by the smoke from the piles. The sensitivity is 5{mu}R/h. A.D.I.R. - This autonomous and portable instrument is designed for the instantaneous measurement of the radon content of the atmosphere in mines. It allows the measurement of contents in air varying between 0.4 and 400 x 10{sup -10} curie per litre of air (0.4 and 400 MPD). The measurement of radioactive fall-out is carried out after collection of this activity by a special rain gauge which comprises an adhesive surface and a tube containing ion exchange resins. The radioactivity of the fall-out varies between some 10{sup -9} and some 10{sup -7} curie per square metre per month. Concentrations in fission products of the atmosphere are measured after collecting on filter paper. Concentrations measured in air at ground level vary between 10{sup -13} and 10{sup -12} curie per cubic metre. (author

  5. Oxidative potential of size-fractionated atmospheric aerosol in urban and rural sites across Europe.

    Science.gov (United States)

    Shafer, Martin M; Hemming, Jocelyn D C; Antkiewicz, Dagmara S; Schauer, James J

    2016-07-18

    In this study we applied several assays, an in vitro rat alveolar macrophage model, a chemical ROS probe (DTT, dithiothreitol), and cytokine induction (TNFα) to examine relationships between PM-induced generation of reactive oxygen species (ROS) and PM composition, using a unique set of size-resolved PM samples obtained from urban and rural environments across Europe. From April-July 2012, we collected PM from roadside canyon, roadside motorway, and background urban sites in each of six European cities and from three rural sites spanning the continent. A Hi-Vol sampler was used to collect PM in three size classes (PM>7, PM7-3, PM3) and PM was characterized for total elements, and oxidative activity quantified in unfiltered and filtered PM extracts. We measured a remarkable uniformity in air concentrations of ROS and especially DTT activity across the continent. Only a 4-fold difference was documented for DTT across the urban sites and a similar variance was documented for ROS, implying that chemical drivers of oxidative activity are relatively similar between sites. The ROS and DTT specific activity was greater at urban background sites (and also rural sites) than at urban canyon locations. PM3 dominated the size distribution of both ROS activity (86% of total) and DTT activity (76% of total), reflecting both the large contribution of PM3 to total PM mass levels and importantly the higher specific oxidative activity of the PM3 in comparison with the larger particles. The soluble fraction of total activity was very high for DTT (94%) as well as for ROS (64%) in the PM3. However in the larger PM size fractions the contributions of the insoluble components became increasingly significant. The dominance of the insoluble PM drivers of activity was particularly evident in the TNFα data, where the insoluble contribution to cytokine production could be 100-fold greater than that from soluble components. ROS and DTT activity were strongly correlated in the PM3 (r = 0

  6. Biomass Burning and Natural Emissions in the Brazilian Amazon Rainforest: Chemical Composition and Impact on the Oxidative Capacity of the Atmosphere

    Science.gov (United States)

    dos Santos, F. C.; Longo, K.; Guenther, A. B.; Gu, D.; Kim, S.; Freitas, S.; Moreira, D. S.; Flávio, L.; Braz, R.; Brito, J.; Oram, D.; Foster, G.; Lee, J. D.

    2017-12-01

    Emitted by vegetation, isoprene (2-methyl-1,3-butadiene) is the most abundant non-methane hydrocarbons, with an annual global emission calculated ranging from 440 to 660Tg carbon, depending on the driving variables like temperature, solar radiation, LAI and PFT. The natural compounds like isoprene and terpenes present in the troposphere are about 90% and 50%, respectively, removed from the atmosphere by oxidation performed by hydroxyl radical (OH). Considering the importance of these emissions and the hydroxyl radical reaction in the atmosphere, the SAMBBA (South American Biomass Burning Analysis) experiment, which occurred during the dry season (September 2012) in the Brazilian Amazon Rainforest, provided information about the chemical composition of the atmosphere through airborne observations. Although primarily focused on biomass burning flights, the SAMBBA project carried out flights in pristine environment. In this study, we determine the ambient distribution of CO, NOx and O3, and evaluate the oxidative capacity of the Amazon rainforest in different chemical regimes, using the ratio [MVK + MACR]/[Isoprene]. Beyond that, we proposed an improvement on the formulation of indirect OH density calculation, using the photochemical aging [O3]/[CO] as a parameter. Balancing numerical modeling and direct observations, the numerical model BRAMS was coupled to MEGAN emission model to get a better result for isoprene and OH in the atmosphere, representing the observations during SAMBBA field campaign. In relation to OH estimation, we observed an improvement in the concentration values using the modified sequential reaction model, for both biomass burning regimes and background environment. We also detected a long-range transport events of O3, considering the high levels of O3 in aged plumes at high altitudes (5,500 - 6,500 m), and the detection of an O3 inflow in the Amazon basin from Africa. These findings support the importance of long-range transport events as a

  7. Direct transformation of calcium sulfite to {alpha}-calcium sulfate hemihydrate in a concentrated Ca-Mg-Mn chloride solution under atmospheric pressure

    Energy Technology Data Exchange (ETDEWEB)

    Baohong Guan; Hailu Fu; Jie Yu; Guangming Jiang; Bao Kong; Zhongbiao Wu [Zhejiang University, Hangzhou (China). Department of Environmental Engineering

    2011-01-15

    Massive quantities of sulfite-rich flue gas desulfurization (FGD) scrubber sludge have been generated by coal burning power plants. Utilization of the sulfite-rich sludge for preparing {alpha}-calcium sulfate hemihydrate ({alpha}-HH), an important kind of cementitious material, is of particular interest to electric utilities and environmental preservation. In the experiment, calcium sulfite hemihydrate was directly transformed to {alpha}-HH without the occurrence of calcium sulfate dihydrate (DH). The transformation was performed in a concentrated CaCl{sub 2} solution containing Mg{sup 2+} and Mn{sup 2+} at 95{sup o}C, atmospheric pressure and low pH. The oxidation of calcium sulfite and the subsequent crystallization of {alpha}-HH constitute the whole conversion, during which the oxidation turns out to be the rate controlling step. Solid solution comprised of calcium sulfite hemihydrate and calcium sulfate was found to coexist with {alpha}-HH in the suspension. Calcium sulfate increases and calcium sulfite decreases spontaneously until the solid solution disappears. Thus, it is a potential alternative to utilize sulfite-rich FGD scrubber sludge for the direct preparation of {alpha}-HH. 36 refs., 10 figs., 1 tab.

  8. Simple proxies for estimating the concentrations of monoterpenes and their oxidation products at a boreal forest site

    Directory of Open Access Journals (Sweden)

    J. Kontkanen

    2016-10-01

    Full Text Available The oxidation products of monoterpenes likely have a crucial role in the formation and growth of aerosol particles in boreal forests. However, the continuous measurements of monoterpene concentrations are usually not available on decadal timescales, and the direct measurements of the concentrations of monoterpene oxidation product have so far been scarce. In this study we developed proxies for the concentrations of monoterpenes and their oxidation products at a boreal forest site in Hyytiälä, southern Finland. For deriving the proxies we used the monoterpene concentration measured with a proton transfer reaction mass spectrometer (PTR-MS during 2006–2013. Our proxies for the monoterpene concentration take into account the temperature-controlled emissions from the forest ecosystem, the dilution caused by the mixing within the boundary layer and different oxidation processes. All the versions of our proxies captured the seasonal variation of the monoterpene concentration, the typical proxy-to-measurements ratios being between 0.8 and 1.3 in summer and between 0.6 and 2.6 in winter. In addition, the proxies were able to describe the diurnal variation of the monoterpene concentration rather well, especially in summer months. By utilizing one of the proxies, we calculated the concentration of oxidation products of monoterpenes by considering their production in the oxidation and their loss due to condensation on aerosol particles. The concentration of oxidation products was found to have a clear seasonal cycle, with a maximum in summer and a minimum in winter. The concentration of oxidation products was lowest in the morning or around noon and highest in the evening. In the future, our proxies for the monoterpene concentration and their oxidation products can be used, for example, in the analysis of new particle formation and growth in boreal environments.

  9. Size resolved mass concentration and elemental composition of atmospheric aerosols over the Eastern Mediterranean area

    Directory of Open Access Journals (Sweden)

    J. Smolík

    2003-01-01

    Full Text Available A Berner low pressure impactor was used to collect size-segregated aerosol samples at Finokalia, located on the north-eastern coast of Crete, Greece during July 2000 and January 2001. Several samples were also collected during the summer campaign aboard the research vessel "AEGAIEO" in the Aegean Sea. Gravimetric analysis and inversion techniques yielded daily PM1 and PM10 mass concentrations. The samples were also analysed by PIXE giving the elemental size distributions of Al, Si, K, Ca, Ti, Mn, Fe, Sr, S, Cl, Ni, V, Cu, Cr, Zn, and Pb. The crustal elements and sea-salt had a unimodal supermicron size distribution. Sulphur was found predominantly in submicron fractions. K, V, and Ni exhibited a bimodal distribution with a submicron mode produced by forest fires and oil combustion. The anthropogenic elements had broad and not well-defined distributions. The time series for PM1 and PM10 mass and elemental concentrations showed both daily and seasonal variation. Higher mass concentrations were observed during two incursions of Saharan dust, whilst higher concentrations of S, Cu, Zn, and Pb were encountered in samples collected in air masses arriving from northern Greece or the western coast of Turkey. Elevated concentrations of chlorine were found in samples with air masses either originating above the Atlantic Ocean and arriving at Finokalia via western Europe or recirculating over the western coast of the Black Sea.

  10. Growth and {delta}{sup 13}C responses to increasing atmospheric carbon dioxide concentrations for several crop species

    Energy Technology Data Exchange (ETDEWEB)

    Hanba, Y.T.; Wada, E. [Center for Ecological Research, Kyoto University, Kyoto (Japan); Osaki, M.; Nakamura, T. [Faculty of Agriculture, Hokkaido University, Hokkaido (Japan)

    1996-04-01

    The responses of plant growth and carbon isotope discrimination ({Delta}) to elevated atmospheric CO{sub 2} concentrations for several crop species (lettuce: Lactuca sativa L.; corn: Zea Mays L. var. P3540, wheat: Triticum aestivum L. var Haruyutaka; and soybean: Glycine Max (L). Merr. var. Kitamusume) were investigated. Shoot relative growth rate was used to indicate plant growth, and {delta}{sup 13}C value of leaf materials in corn (C4 species) was used to calculate {Delta} for C3 species. Plant growth was stimulated by enriched CO{sub 2}, while {Delta} remained almost constant as CO{sub 2} concentration changed. {Delta} showed interspecific difference, and the plant species of larger {Delta} had larger relative growth rates. Relative growth rates of the plants of larger {Delta} were stimulated by CO{sub 2} enrichment more than those of the plants of smaller {Delta}. We propose that plant {Delta} could be a possible parameter to assess the interspecific difference of plant response to the increasing atmospheric CO{sub 2} concentrations. 3 figs., 2 tabs., 25 refs.

  11. Oxidative stress responses of submerged macrophyte Vallisneria asiatica to different concentrations of cyanobacteria

    Science.gov (United States)

    Kang, Caixia; Kuba, Takahiro; Hao, Aimin; Iseri, Yasushi; Li, Chunjie; Zhang, Zhenjia

    2015-03-01

    In a 10-day aquarium experiment, this investigation examines macrophyte restoration in eutrophic Lake Taihu, the physiological effects of different plant biomass levels and of increasing natural cyanobacterial concentrations on a submerged macrophyte, Vallisneria asiatica. Cyanobacterial stress suppressed the superoxide dismutase (SOD) activity of the plant's leaves and induced the catalase (CAT) and peroxidase (POD) activities of its roots. The soluble protein content in V. asiatica decreased with an increase in natural cyanobacterial concentrations, whereas the malonaldehyde (MDA) increased significantly at chlorophyll a (Chl a) concentrations of 222 and 262 μg/L in water. V. asiatica adapted to the stress caused by cyanobacterial concentrations by adjusting its antioxidant defense system to remove the excessive reactive oxygen species when the algal Chl a concentration was >109 μg/L. Additionally, high biomass of V. asiatica (2 222 g FW/m2) can inhibit the reproduction of cyanobacteria more significantly than low biomass (1 111 g FW/m2). High biomass of V. asiatica increased the oxidative stress in an individual plant when the initial Chl a concentration in the water reached 222 and 262 μg/L, as expressed by the increased MDA in leaves, compared with low biomass of V. asiatica. This provides a basis for controlling cyanobacterial concentrations and V. asiatica biomass for the recovery of V. asiatica in eutrophic Lake Taihu.

  12. Fighting global warming by greenhouse gas removal: destroying atmospheric nitrous oxide thanks to synergies between two breakthrough technologies.

    Science.gov (United States)

    Ming, Tingzhen; de Richter, Renaud; Shen, Sheng; Caillol, Sylvain

    2016-04-01

    Even if humans stop discharging CO2 into the atmosphere, the average global temperature will still increase during this century. A lot of research has been devoted to prevent and reduce the amount of carbon dioxide (CO2) emissions in the atmosphere, in order to mitigate the effects of climate change. Carbon capture and sequestration (CCS) is one of the technologies that might help to limit emissions. In complement, direct CO2 removal from the atmosphere has been proposed after the emissions have occurred. But, the removal of all the excess anthropogenic atmospheric CO2 will not be enough, due to the fact that CO2 outgases from the ocean as its solubility is dependent of its atmospheric partial pressure. Bringing back the Earth average surface temperature to pre-industrial levels would require the removal of all previously emitted CO2. Thus, the atmospheric removal of other greenhouse gases is necessary. This article proposes a combination of disrupting techniques to transform nitrous oxide (N2O), the third most important greenhouse gas (GHG) in terms of current radiative forcing, which is harmful for the ozone layer and possesses quite high global warming potential. Although several scientific publications cite "greenhouse gas removal," to our knowledge, it is the first time innovative solutions are proposed to effectively remove N2O or other GHGs from the atmosphere other than CO2.

  13. Passive Sampler for Measurements of Atmospheric Nitric Acid Vapor (HNO3 Concentrations

    Directory of Open Access Journals (Sweden)

    Andrzej Bytnerowicz

    2001-01-01

    Full Text Available Nitric acid (HNO3 vapor is an important nitrogenous air pollutant responsible for increasing saturation of forests with nitrogen and direct injury to plants. The USDA Forest Service and University of California researchers have developed a simple and inexpensive passive sampler for monitoring air concentrations of HNO3. Nitric acid is selectively absorbed on 47-mm Nylasorb nylon filters with no interference from particulate NO3-. Concentrations determined with the passive samplers closely corresponded with those measured with the co-located honeycomb annular denuder systems. The PVC protective caps of standardized dimensions protect nylon filters from rain and wind and allow for reliable measurements of ambient HNO3 concentrations. The described samplers have been successfully used in Sequoia National Park, the San Bernardino Mountains, and on Mammoth Mountain in California.

  14. Atmospheric Plasma Spraying Low-Temperature Cathode Materials for Solid Oxide Fuel Cells

    Science.gov (United States)

    Harris, J.; Kesler, O.

    2010-01-01

    Atmospheric plasma spraying (APS) is attractive for manufacturing solid oxide fuel cells (SOFCs) because it allows functional layers to be built rapidly with controlled microstructures. The technique allows SOFCs that operate at low temperatures (500-700 °C) to be fabricated by spraying directly onto robust and inexpensive metallic supports. However, standard cathode materials used in commercial SOFCs exhibit high polarization resistances at low operating temperatures. Therefore, alternative cathode materials with high performance at low temperatures are essential to facilitate the use of metallic supports. Coatings of lanthanum strontium cobalt ferrite (LSCF) were fabricated on steel substrates using axial-injection APS. The thickness and microstructure of the coating layers were evaluated, and x-ray diffraction analysis was performed on the coatings to detect material decomposition and the formation of undesired phases in the plasma. These results determined the envelope of plasma spray parameters in which coatings of LSCF can be manufactured, and the range of conditions in which composite cathode coatings could potentially be manufactured.

  15. Microstructural evaluation of ceria-samaria-gadolinia-nickel oxide composite after reduction in hydrogen atmosphere

    International Nuclear Information System (INIS)

    Arakaki, A. R.; Yoshito, W.K.; Ussui, V.; Lazar, D.R.R.

    2012-01-01

    The ceria-samaria-gadolinia-nickel composite (Ni-SGDC), used as Solid Oxide Fuel Cell (SOFC) anode, was obtained by 'in situ' reduction of NiO-SGDC, with composition Ce 0,8 (SmGd) 0,2 O 1,9 /NiO and mass proportion 40:60%. The composite was produced by hydroxides coprecipitation using CTAB surfactant, followed by solvothermal treatment in butanol, calcination at 600 deg C, pressing and sintering at 1350 deg C for 1 h. The composite reduction kinetic was evaluated in a tubular furnace under dynamic atmosphere of 4% H2 /Air, fixing the temperature at 900 deg C and time between 10 and 120 minutes. The microstructural characterization was performed by optical and scanning electron microscopy. The samples were characterized either by X-ray diffraction and density measurements by immersion technique in water. It was verified that the NiO reduced fraction reached values between 80 and 90% and the achieved porosity (about 30%) is acceptable to a good anode performance (author)

  16. Effects of cocoa powder and dark chocolate on LDL oxidative susceptibility and prostaglandin concentrations in humans.

    Science.gov (United States)

    Wan, Y; Vinson, J A; Etherton, T D; Proch, J; Lazarus, S A; Kris-Etherton, P M

    2001-11-01

    Flavonoids are polyphenolic compounds of plant origin with antioxidant effects. Flavonoids inhibit LDL oxidation and reduce thrombotic tendency in vitro. Little is known about how cocoa powder and dark chocolate, rich sources of polyphenols, affect these cardiovascular disease risk factors. We evaluated the effects of a diet high in cocoa powder and dark chocolate (CP-DC diet) on LDL oxidative susceptibility, serum total antioxidant capacity, and urinary prostaglandin concentrations. We conducted a randomized, 2-period, crossover study in 23 healthy subjects fed 2 diets: an average American diet (AAD) controlled for fiber, caffeine, and theobromine and an AAD supplemented with 22 g cocoa powder and 16 g dark chocolate (CP-DC diet), providing approximately 466 mg procyanidins/d. LDL oxidation lag time was approximately 8% greater (P = 0.01) after the CP-DC diet than after the AAD. Serum total antioxidant capacity measured by oxygen radical absorbance capacity was approximately 4% greater (P = 0.04) after the CP-DC diet than after the AAD and was positively correlated with LDL oxidation lag time (r = 0.32, P = 0.03). HDL cholesterol was 4% greater after the CP-DC diet (P = 0.02) than after the AAD; however, LDL-HDL ratios were not significantly different. Twenty-four-hour urinary excretion of thromboxane B(2) and 6-keto-prostaglandin F(1)(alpha) and the ratio of the 2 compounds were not significantly different between the 2 diets. Cocoa powder and dark chocolate may favorably affect cardiovascular disease risk status by modestly reducing LDL oxidation susceptibility, increasing serum total antioxidant capacity and HDL-cholesterol concentrations, and not adversely affecting prostaglandins.

  17. Local variations of atmospheric 222Rn and 210Pb concentrations in Badgastein (Austria)

    International Nuclear Information System (INIS)

    Wallner, G.; Ayromlou, S.

    2002-01-01

    222 Rn was measured and aerosols for 210 Pb determination were collected simultaneously outdoors at ground level near the train station of Badgastein (1080 m a.s.l.), and later on also on the nearby Stubnerkogel (2230 m a.s.l.). Radon concentrations at lower altitude were up to 140 Bq/m 3 , on the mountain the usual background levels were found. In contrary to the differing radon levels, the 210 Pb activity concentrations were in the same order of magnitude for both locations with values between 0.16 and 0.77 mBq/m 3 . (author)

  18. Changes in concentration and (delta) 13C value of dissolved CH4, CO2 and organic carbon in rice paddies under ambient and elevated concentrations of atmospheric CO2

    International Nuclear Information System (INIS)

    Weiguo Cheng; Yagi, Kazuyuki; Sakai, Hidemitsu; Hua Xu; Kobayashi, Kazuhiko

    2005-01-01

    Changes in concentration and (delta) 13 C value of dissolved CH 4 , CO 2 and organic carbon (DOC) in floodwater and soil solution from a Japanese rice paddy were studied under ambient and elevated concentrations of atmospheric CO 2 in controlled environment chambers. The concentrations of dissolved CH 4 in floodwater increased with rice growth (with some fluctuation), while the concentrations of CO 2 remained between 2.9 to 4.4 and 4.2 to 5.8 μg C mL -1 under conditions of ambient and elevated CO 2 concentration, respectively. The amount of CH 4 dissolved in soil solution under elevated CO 2 levels was significantly lower than under ambient CO 2 in the tillering stage, implying that the elevated CO 2 treatment accelerated CH 4 oxidation during the early stage of growth. However, during later stages of growth, production of CH 4 increased and the amount of CH 4 dissolved in soil solution under elevated CO 2 levels was, on average, greater than that under ambient CO 2 conditions. Significant correlation existed among the (delta) 13 C values of dissolved CH 4 , CO 2 , and DOC in floodwater (except for the samples taken immediately after pulse feeding with 13 C enriched CO 2 ), indicating that the origins and cycling of CH 4 , CO 2 and DOC were related. There were also significant correlations among the (delta) 13 C values of CH 4 , CO 2 and DOC in the soil solution. The turnover rate of CO 2 in soil solution was most rapid in the panicle formation stage of rice growth and that of CH 4 fastest in the grain filling stage. (Author)

  19. Electro-Fenton oxidation of reverse osmosis concentrate from sanitary landfill leachate: Evaluation of operational parameters.

    Science.gov (United States)

    Fernandes, Annabel; Labiadh, Lazhar; Ciríaco, Lurdes; Pacheco, Maria José; Gadri, Abdellatif; Ammar, Salah; Lopes, Ana

    2017-10-01

    The electro-Fenton oxidation of a concentrate from reverse osmosis of a sanitary landfill leachate, with an initial chemical oxygen demand (COD) of 42 g L -1 , was carried out using a carbon-felt cathode and a boron doped diamond anode. The influence of the applied current intensity, initial pH and dissolved iron initial concentration on the electro-Fenton process was assessed. For the experimental conditions used, results showed that the initial pH is the parameter that more strongly influences the current efficiency of the electro-Fenton process, being this influence more pronounced on the oxidation rate than on the mineralization rate of the organic matter. The increase in iron initial concentration was found to be detrimental, since the natural amount of iron present in the effluent, 73 mg L -1 of total iron and 61 mg L -1 of dissolved iron, was sufficient to ensure the electro-Fenton process at the applied intensities - 0.2-1.4 A. For the more favourable conditions studied, initial pH of 3 and natural iron concentration, it was found an increase in the organic load and nitrogen removals with the applied current intensity. For the highest current intensity applied, a COD removal of 16.7 g L -1 was achieved after 8-h experiments. Copyright © 2017 Elsevier Ltd. All rights reserved.

  20. Stabilization of arsenic and lead by magnesium oxide (MgO) in different seawater concentrations.

    Science.gov (United States)

    Kameda, Kentaro; Hashimoto, Yohey; Ok, Yong Sik

    2018-02-01

    Ongoing sea level rise will have a major impact on mobility and migration of contaminants by changing a number of natural phenomena that alter geochemistry and hydrology of subsurface environment. In-situ immobilization techniques may be a promising remediation strategy for mitigating contaminant mobility induced by sea level rise. This study investigated the reaction mechanisms of magnesium oxide (MgO) with aqueous Pb and As under freshwater and seawater using XAFS spectroscopy. Initial concentrations of Pb and As in freshwater strongly controlled the characteristics of the reaction product of MgO. Our study revealed that i) the removal of aqueous Pb and As by MgO was increased by the elevation of seawater concentration, and ii) the removal of As was attributed primarily to (inner-sphere) surface adsorption on MgO, independent on seawater concentrations, and iii) the retention mechanism of Pb was dependent on seawater concentrations where formations of Pb oxides and adsorption on the MgO surface were predominant in solutions with low and high salinity, respectively. The release of As fixed with MgO significantly increased in seawater compared to freshwater, although the amount of As desorbed accounted for <0.2% of total As. Copyright © 2017 Elsevier Ltd. All rights reserved.

  1. Inverse constraints for emission fluxes of atmospheric tracers estimated from concentration measurements and Lagrangian transport

    Science.gov (United States)

    Pisso, Ignacio; Patra, Prabir; Breivik, Knut

    2015-04-01

    Lagrangian transport models based on times series of Eulerian fields provide a computationally affordable way of achieving very high resolution for limited areas and time periods. This makes them especially suitable for the analysis of point-wise measurements of atmospheric tracers. We present an application illustrated with examples of greenhouse gases from anthropogenic emissions in urban areas and biogenic emissions in Japan and of pollutants in the Arctic. We asses the algorithmic complexity of the numerical implementation as well as the use of non-procedural techniques such as Object-Oriented programming. We discuss aspects related to the quantification of uncertainty from prior information in the presence of model error and limited number of observations. The case of non-linear constraints is explored using direct numerical optimisation methods.

  2. Modeling Caspian Sea water level oscillations under different scenarios of increasing atmospheric carbon dioxide concentrations

    Directory of Open Access Journals (Sweden)

    Roshan GholamReza

    2012-12-01

    Full Text Available Abstract The rapid rise of Caspian Sea water level (about 2.25 meters since 1978 has caused much concern to all five surrounding countries, primarily because flooding has destroyed or damaged buildings and other engineering structures, roads, beaches and farm lands in the coastal zone. Given that climate, and more specifically climate change, is a primary factor influencing oscillations in Caspian Sea water levels, the effect of different climate change scenarios on future Caspian Sea levels was simulated. Variations in environmental parameters such as temperature, precipitation, evaporation, atmospheric carbon dioxide and water level oscillations of the Caspian sea and surrounding regions, are considered for both past (1951-2006 and future (2025-2100 time frames. The output of the UKHADGEM general circulation model and five alternative scenarios including A1CAI, BIASF, BIMES WRE450 and WRE750 were extracted using the MAGICC SCENGEN Model software (version 5.3. The results suggest that the mean temperature of the Caspian Sea region (Bandar-E-Anzali monitoring site has increased by ca. 0.17°C per decade under the impacts of atmospheric carbon dioxide changes (r=0.21. The Caspian Sea water level has increased by ca. +36cm per decade (r=0.82 between the years 1951-2006. Mean results from all modeled scenarios indicate that the temperature will increase by ca. 3.64°C and precipitation will decrease by ca. 10% (182 mm over the Caspian Sea, whilst in the Volga river basin, temperatures are projected to increase by ca. 4.78°C and precipitation increase by ca. 12% (58 mm by the year 2100. Finally, statistical modeling of the Caspian Sea water levels project future water level increases of between 86 cm and 163 cm by the years 2075 and 2100, respectively.

  3. Modeling Caspian Sea water level oscillations under different scenarios of increasing atmospheric carbon dioxide concentrations.

    Science.gov (United States)

    Roshan, Gholamreza; Moghbel, Masumeh; Grab, Stefan

    2012-12-12

    The rapid rise of Caspian Sea water level (about 2.25 meters since 1978) has caused much concern to all five surrounding countries, primarily because flooding has destroyed or damaged buildings and other engineering structures, roads, beaches and farm lands in the coastal zone. Given that climate, and more specifically climate change, is a primary factor influencing oscillations in Caspian Sea water levels, the effect of different climate change scenarios on future Caspian Sea levels was simulated. Variations in environmental parameters such as temperature, precipitation, evaporation, atmospheric carbon dioxide and water level oscillations of the Caspian sea and surrounding regions, are considered for both past (1951-2006) and future (2025-2100) time frames. The output of the UKHADGEM general circulation model and five alternative scenarios including A1CAI, BIASF, BIMES WRE450 and WRE750 were extracted using the MAGICC SCENGEN Model software (version 5.3). The results suggest that the mean temperature of the Caspian Sea region (Bandar-E-Anzali monitoring site) has increased by ca. 0.17°C per decade under the impacts of atmospheric carbon dioxide changes (r=0.21). The Caspian Sea water level has increased by ca. +36cm per decade (r=0.82) between the years 1951-2006. Mean results from all modeled scenarios indicate that the temperature will increase by ca. 3.64°C and precipitation will decrease by ca. 10% (182 mm) over the Caspian Sea, whilst in the Volga river basin, temperatures are projected to increase by ca. 4.78°C and precipitation increase by ca. 12% (58 mm) by the year 2100. Finally, statistical modeling of the Caspian Sea water levels project future water level increases of between 86 cm and 163 cm by the years 2075 and 2100, respectively.

  4. Temporal variability of atmospheric radon-222 concentration at Gosan Station, Jeju Island, Korea, during 2009-2013

    Energy Technology Data Exchange (ETDEWEB)

    Song, Jung Min; Kim, Won Hyung; Kang, Chang Hee [Dept. of Chemistry, Jeju National University, Jeju (Korea, Republic of); Lee, Hae Young; Lee, Chul Kyu [Korea Global Atmosphere Watch Center, Korea Meteorological Administration, ChungNam (Korea, Republic of); Chambers, S.; Williams, A. G. [Australian Nuclear Science and Technology Organisation, Kirrawee DC (Australia)

    2015-02-15

    Atmospheric radon-222 (radon) measurements were made from 2009 to 2013 at the Gosan station of Jeju Island, one of the cleanest regions in Korea, in order to characterize the temporal variability (on diurnal, seasonal, and annual scales) and analyze the influence of changing air mass transport pathways on observed radon concentrations. The mean hourly radon concentration over the whole period was 2441 ± 1037 mBq/m{sup 3}. The seasonal cycle of radon at the Gosan station was characterized by a fall maximum and summer minimum, consistent with a reduction in nonfrozen terrestrial fetch from fall to summer. In order, the seasonal mean radon concentrations were 2962 mBq/m{sup 3} (fall) >2907 mBq/m{sup 3} (winter) >2219 mBq/m{sup 3} (spring) >1756 mBq/m{sup 3} (summer). Based on a 5-year composite, the maximum mean monthly radon concentration in October (3100 mBq/m{sup 3}) was more than twice the July minimum (1471 mBq/m{sup 3}). Diurnal composite radon concentrations for the whole period increased throughout the night to a maximum of 2788 mBq/m{sup 3} at around 7 a.m., and then gradually decreased to a minimum of 2050 mBq/m{sup 3} at around 3 p.m. The winter diurnal cycle had a small amplitude due to the low variability in atmospheric mixing depth associated with recent air mass fetch over the Yellow Sea. The diurnal cycle in summer, however, exhibited a relatively large amplitude due to changes in atmospheric mixing depth associated with recent fetch over Jeju Island. Back trajectory analysis showed that high radon events were typically associated with long-term air mass fetch over continental Asia. Specifically, the average radon concentration of air masses originating from China was about 2.4 times higher than that of air masses originating from the North Pacific Ocean.

  5. Temporal variability of atmospheric radon-222 concentration at Gosan Station, Jeju Island, Korea, during 2009-2013

    International Nuclear Information System (INIS)

    Song, Jung Min; Kim, Won Hyung; Kang, Chang Hee; Lee, Hae Young; Lee, Chul Kyu; Chambers, S.; Williams, A. G.

    2015-01-01

    Atmospheric radon-222 (radon) measurements were made from 2009 to 2013 at the Gosan station of Jeju Island, one of the cleanest regions in Korea, in order to characterize the temporal variability (on diurnal, seasonal, and annual scales) and analyze the influence of changing air mass transport pathways on observed radon concentrations. The mean hourly radon concentration over the whole period was 2441 ± 1037 mBq/m"3. The seasonal cycle of radon at the Gosan station was characterized by a fall maximum and summer minimum, consistent with a reduction in nonfrozen terrestrial fetch from fall to summer. In order, the seasonal mean radon concentrations were 2962 mBq/m"3 (fall) >2907 mBq/m"3 (winter) >2219 mBq/m"3 (spring) >1756 mBq/m"3 (summer). Based on a 5-year composite, the maximum mean monthly radon concentration in October (3100 mBq/m"3) was more than twice the July minimum (1471 mBq/m"3). Diurnal composite radon concentrations for the whole period increased throughout the night to a maximum of 2788 mBq/m"3 at around 7 a.m., and then gradually decreased to a minimum of 2050 mBq/m"3 at around 3 p.m. The winter diurnal cycle had a small amplitude due to the low variability in atmospheric mixing depth associated with recent air mass fetch over the Yellow Sea. The diurnal cycle in summer, however, exhibited a relatively large amplitude due to changes in atmospheric mixing depth associated with recent fetch over Jeju Island. Back trajectory analysis showed that high radon events were typically associated with long-term air mass fetch over continental Asia. Specifically, the average radon concentration of air masses originating from China was about 2.4 times higher than that of air masses originating from the North Pacific Ocean

  6. Spatial and Temporal Variability of CO2 and CH4 Concentrations in the Atmospheric Surface Layer over West Siberia

    Science.gov (United States)

    Belan, Boris D.; Machida, Toshinobu; Sasakawa, Motoki; Davydov, Denis K.; Fofonov, Alexander V.; Krasnov, Oleg A.; Maksyutov, Shamil; Arshinov, Mikhail Yu.

    2015-04-01

    The investigation of greenhouse gas behavior in the atmosphere plays a key role in predicting the global changes of Earth's climate. In this connection, of particular importance is the study of the distribution of sources/sinks of trace gases in the atmospheric surface layer over the different regions of the globe. In order to fill a gap in the data on greenhouse gas concentrations in Russia, National Institute for Environmental Studies (NIES, Japan) and Institute of Atmospheric Optics (IAO SB RAS, Russia) established a network for GHG monitoring (JR-STATION, Japan-Russia Siberian Tall Tower Inland Observation Network). Gas analyzers and meteorological sensors were mounted at radio relay towers located in different regions of West Siberia. The checking equipment was placed in containers at the tower base. In the containers, the climatic parameters optimal for gas analyzer operation were maintained. The work on the network development started in 2001. Since at each of the sites the measurement duration could be different, in this paper we present the data of the greenhouse gas monitoring for eight sites which give the primary idea on the spatial distribution and temporal dynamics of CO2 and CH4 in the atmospheric surface layer over West Siberia. The analysis of the data showed that the average increase in concentration of carbon dioxide by results of our measurements in this territory increases within 1.95 - 2.53 ppm/year, depending on the area. The analysis of long-term data testifies about existence of growth of concentration of methane within 3.2 - 7.2 ppb / year. The presence of a distributed network of the sites operating in the monitoring regime makes it possible not only to investigate the temporal dynamics of CO2 and CH4 at each site and to determine the spatial differences between the concentrations by comparing the data, but also to plot the distribution charts for different moments of time. This work was supported by the Global Environment Research

  7. Observed and Modeled Tritium Concentrations in the Terrestrial Food Chain near a Continuous Atmospheric Source

    International Nuclear Information System (INIS)

    Davis, P.A.; Kim, S.B.; Chouhan, S.L.; Workman, W.J.G.

    2005-01-01

    Tritium concentrations were measured in a large number of environmental and biological samples collected during 2002 at two dairy farms and a hobby farm near Pickering Nuclear Generating Station in Ontario, Canada. The data cover most compartments of the terrestrial food chain in an agricultural setting and include detailed information on the diets of the local farm animals. Ratios of plant OBT concentration to air moisture HTO varied between 0.12 and 0.56, and were generally higher for the forage crops collected at the dairy farms than for the garden vegetables sampled at the hobby farm. Animal OBT to air HTO ratios were more uniform, ranging from 0.18 to 0.45, and were generally higher for the milk and beef samples from the dairy farms than for the chicken products from the hobby farm. The observed OBT concentrations in plants and animals were compared with predictions of IMPACT, the model used by the Canadian nuclear industry to calculate annual average doses due to routine releases. The model performed well on average for the animal endpoints but overestimated concentrations in plants by a factor of 2

  8. Advanced Oxidation Processes (AOPs for Refinery Wastewater Treatment Contains High Phenol Concentration

    Directory of Open Access Journals (Sweden)

    Azizah Alif Nurul

    2018-01-01

    Full Text Available Petroleum Refinery wastewater is characterized by a high phenol content. Phenol is toxic and resistant to biological processes for treatment of the petroleum refinery wastewater. The combination of an AOP and a biological process can be used for treatment of the refinery wastewater. It is necessary to conduct a study to determine the appropriate condition of AOP to meet the phenol removal level. Two AOP configurations were investigated: H2O2 / UV and H2O2 / UV / O3. From each process samples, COD, phenol and pH were measured. The oxidation was carried out until the targeted phenol concentration of treated effluent were obtained. The better result obtained by using process H2O2 / UV / O3 with the H2O2 concentration 1000 ppm. After 120 minutes, the final target has been achieved in which phenol concentration of 37.5 mg/L or phenol degradation of 93.75%.

  9. Atmospheric concentrations and phase partitioning of polycyclic aromatic hydrocarbons in Izmir, Turkey

    Energy Technology Data Exchange (ETDEWEB)

    Demircioglu, Eylem; Odabasi, Mustafa [Faculty of Engineering, Department of Environmental Engineering, Dokuz Eylul University, Izmir (Turkey); Sofuoglu, Aysun [Faculty of Engineering, Department of Chemical Engineering, Izmir Institute of Technology, Gulbahce-Urla (Turkey)

    2011-04-15

    Ambient air polycyclic aromatic hydrocarbon (PAH) samples were collected at a suburban (n = 63) and at an urban site (n = 14) in Izmir, Turkey. Average gas-phase total PAH (sum {sub 14}PAH) concentrations were 23.5 ng m{sup -3} for suburban and 109.7 ng m{sup -3} for urban sites while average particle-phase total PAH concentrations were 12.3 and 34.5 ng m{sup -3} for suburban and urban sites, respectively. Higher ambient PAH concentrations were measured in the gas-phase and sum {sub 14}PAH concentrations were dominated by lower molecular weight PAHs. Multiple linear regression analysis indicated that the meteorological parameters were effective on ambient PAH concentrations. Emission sources of particle-phase PAHs were investigated using a diagnostic plot of fluorene (FLN)/(fluorine + pyrene; PY) versus indeno[1,2,3-cd]PY/(indeno[1,2,3-cd]PY + benzo[g,h,i]perylene) and several diagnostic ratios. These approaches have indicated that traffic emissions (petroleum combustion) were the dominant PAH sources at both sites for summer and winter seasons. Experimental gas-particle partition coefficients (K{sub P}) were compared to the predictions of octanol-air (K{sub OA}) and soot-air (K{sub SA}) partition coefficient models. The correlations between experimental and modeled K{sub P} values were significant (r{sup 2} = 0.79 and 0.94 for suburban and urban sites, respectively, p < 0.01). Octanol-based absorptive partitioning model predicted lower partition coefficients especially for relatively volatile PAHs. However, overall there was a relatively good agreement between the measured K{sub P} and soot-based model predictions. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  10. Trace concentrations of vitamin E protect radiation crosslinked UHMWPE from oxidative degradation.

    Science.gov (United States)

    Kurtz, S M; Dumbleton, J; Siskey, R S; Wang, A; Manley, M

    2009-08-01

    The effect of very low concentrations of Vitamin E on the stability and mechanical behavior of UHMWPE remains unknown. We tested the hypothesis that the oxidation resistance of Vitamin E-blended UHMWPE would be influenced by trace doses of antioxidant, resin, and radiation treatment. Trace concentrations (Vitamin E) were blended separately with GUR 1020 and 1050 resins and molded into disks. From each disk, three groups of 10 mm thick blocks were machined: (1) no irradiation (control); (2) 30 kGy of gamma irradiation in nitrogen; and (3) 75 kGy of gamma irradiation in air. Specimens were subjected to three aging protocols: (a) no aging (control); (b) two weeks and (c) four weeks of accelerated aging in accordance with ASTM F 2003 (i.e., 70 degrees C and 5 atm oxygen). The minimum concentration of Vitamin E needed to stabilize UHMWPE during our accelerated tests depended upon the method of radiation processing. For the 30 and 75 kGy irradiated materials, the addition of 125 ppm or more Vitamin E was sufficient to maintain baseline mechanical and chemical properties through two weeks of accelerated aging. For these groups, the addition of 375 ppm or 500 ppm, respectively, was necessary to maintain baseline mechanical and chemical properties throughout the four-week accelerated aging period. UHMWPE resin molecular weight did not have an effect on oxidation behavior. The results of this experiment therefore supported our hypotheses that trace concentrations of Vitamin E, coupled with radiation treatment-but not resin grade-influence the mechanical and oxidative degradation behavior of UHMWPE.

  11. Correlation between sub-micron surface roughness of iron oxide encrustations and trace element concentrations

    International Nuclear Information System (INIS)

    Fischer, Cornelius; Karius, Volker; Luettge, Andreas

    2009-01-01

    Iron oxide encrustations are formed on black slate surfaces during oxidative weathering of iron sulfide and phosphate bearing, organic matter-rich slates. Synchronously, trace elements are released during ongoing weathering. Laser ablation ICP-MS analyses of a weathered and encrusted slate showed that major portions of the V, Cu, As, Mo, Pb, Th, and U reside in the encrustation. Recently a potential relationship between several micrometer to 500 nm surface topography roughness of such encrustations and its uranium concentration was shown. Based on laser scanning microscopy measurements, the present study shows that this interrelation must be expanded to small submicron-sized half-pores with diameters between 100 nm and 500 nm. We demonstrate that the relationship is not limited to topography variations of a single encrustation in the hand-specimen scale. Surface topography and geochemical analyses of iron oxide encrustations from several locations but from the same geochemical environment and with similar weathering history showed that the concentrations of U, P, Cu, and Zn correlate inversely with the surface roughness parameter F. This parameter represents the total surface area and is - in this case - a proxy for the root-mean square surface roughness Rq. This study substantiates the environmental importance that micrometer- to submicrometer topography variations of fluid-rock interfaces govern the trapping of trace elements.

  12. Correlation between sub-micron surface roughness of iron oxide encrustations and trace element concentrations

    Energy Technology Data Exchange (ETDEWEB)

    Fischer, Cornelius, E-mail: cornelius@rice.edu [Department of Earth Science, MS-126, Rice University, 6100 Main Street, Houston, TX 77005 (United States); Geowissenschaftliches Zentrum der Universitaet Goettingen, Abt. Sedimentologie and Umweltgeologie, Goldschmidtstr. 3, D-37077 Goettingen (Germany); Karius, Volker [Geowissenschaftliches Zentrum der Universitaet Goettingen, Abt. Sedimentologie and Umweltgeologie, Goldschmidtstr. 3, D-37077 Goettingen (Germany); Luettge, Andreas [Department of Earth Science, MS-126, Rice University, 6100 Main Street, Houston, TX 77005 (United States); Department of Chemistry, Rice University, 6100 Main Street, Houston, TX 77005 (United States)

    2009-08-01

    Iron oxide encrustations are formed on black slate surfaces during oxidative weathering of iron sulfide and phosphate bearing, organic matter-rich slates. Synchronously, trace elements are released during ongoing weathering. Laser ablation ICP-MS analyses of a weathered and encrusted slate showed that major portions of the V, Cu, As, Mo, Pb, Th, and U reside in the encrustation. Recently a potential relationship between several micrometer to 500 nm surface topography roughness of such encrustations and its uranium concentration was shown. Based on laser scanning microscopy measurements, the present study shows that this interrelation must be expanded to small submicron-sized half-pores with diameters between 100 nm and 500 nm. We demonstrate that the relationship is not limited to topography variations of a single encrustation in the hand-specimen scale. Surface topography and geochemical analyses of iron oxide encrustations from several locations but from the same geochemical environment and with similar weathering history showed that the concentrations of U, P, Cu, and Zn correlate inversely with the surface roughness parameter F. This parameter represents the total surface area and is - in this case - a proxy for the root-mean square surface roughness Rq. This study substantiates the environmental importance that micrometer- to submicrometer topography variations of fluid-rock interfaces govern the trapping of trace elements.

  13. A Calibration to Predict Concentrations of Impurities in Plutonium Oxide by Prompt Gamma Analysis

    International Nuclear Information System (INIS)

    Narlesky, J.E.; Kelly, E.J.; Foster, L.A.

    2005-01-01

    Prompt gamma (PG) analysis has been used to identify the presence of certain impurities in plutonium oxide, which has been stored in 3013 containers. A regression analysis was used to evaluate the trends between the count rates obtained from PG analysis and the concentration of the impurities in plutonium oxide samples measured by analytical chemistry techniques. The results of the analysis were used to obtain calibration curves, which may be used to predict the concentration of Al, Be, Cl, F, Mg, and Na in the 3013 containers. The scatter observed in the data resulted from several factors including sample geometry, error in sampling for chemical assay, statistical counting error, and intimacy of mixing of impurities and plutonium. Standards prepared by mixing plutonium oxide with CaF 2 , NaCl, and KCl show that intimacy mixing and sampling error have the largest influence on the results. Although these factors are difficult to control, the calibrations are expected to yield semiquantitative results that are sufficient for the purpose of ordering or ranking

  14. Serum thiamine concentration and oxidative stress as predictors of mortality in patients with septic shock.

    Science.gov (United States)

    Costa, Nara Aline; Gut, Ana Lúcia; de Souza Dorna, Mariana; Pimentel, José Alexandre Coelho; Cozzolino, Silvia Maria Franciscato; Azevedo, Paula Schmidt; Fernandes, Ana Angélica Henrique; Zornoff, Leonardo Antonio Mamede; de Paiva, Sergio Alberto Rupp; Minicucci, Marcos Ferreira

    2014-04-01

    The purpose of the study is to determine the influence of serum thiamine, glutathione peroxidase (GPx) activity, and serum protein carbonyl concentrations in hospital mortality in patients with septic shock. This prospective study included all patients with septic shock on admission or during intensive care unit (ICU) stay, older than 18 years, admitted to 1 of the 3 ICUs of the Botucatu Medical School, from January to August 2012. Demographic information, clinical evaluation, and blood sample were taken within the first 72 hours of the patient's admission or within 72 hours after septic shock diagnosis for serum thiamine, GPx activity, and protein carbonyl determination. One hundred eight consecutive patients were evaluated. The mean age was 57.5 ± 16.0 years, 63% were male, 54.6% died in the ICU, and 71.3% had thiamine deficiency. Thiamine was not associated with oxidative stress. Neither vitamin B1 levels nor the GPx activity was associated with outcomes in these patients. However, protein carbonyl concentration was associated with increased mortality. In patients with septic shock, oxidative stress was associated with mortality. On the other hand, thiamine was not associated with oxidative stress or mortality in these patients. Copyright © 2014 Elsevier Inc. All rights reserved.

  15. Seasonal and diel patterns of total gaseous mercury concentration in the atmosphere of the Central Valley of Costa Rica

    International Nuclear Information System (INIS)

    Castillo, Aylin; Valdes, Juan; Sibaja, Jose; Vega, Ilena; Alfaro, Rosa; Morales, Jose; Esquivel, Germain; Barrantes, Elisa; Black, Paleah; Lean, David

    2011-01-01

    Research highlights: → Elevated seasonal and daily patterns of total gaseous mercury (TGM) were observed in the Central Valley of Costa Rica 27 km south-east of the Poas volcano. → With the onset of the wet season TGM in late April, values increased from typical values near 10 to 905 ng m -3 . → During the day, TGM values increased until midday along with temperature and radiation but relative humidity showed a reciprocal pattern. → We conclude that elemental mercury from the volcano may react with atmospheric oxidants especially during the dry season and the mercury would be deposited to the ground. → With the onset of heavy rains, mercury in the soil is reduced and re-volatilized resulting in the high levels in atmospheric air at the end of April. - Abstract: Monitoring of Hg in the atmosphere near volcanoes is limited with no previous data for Costa Rica. Seasonal and daily patterns of total gaseous mercury (TGM) were observed at the main sampling location at the Universidad Nacional, Heredia, Costa Rica. The area (lat. 10.000230 long. -84.109499) is located in the Central Valley of Costa Rica and is 27 km SE of the Poas volcano (lat. 10.199486 long. -84.231388). Measurements were made from May 2008 to May 2009 at this location with some additional values obtained at other sites near the Poas volcano including San Luis and Grecia as well as near, Turrialba and Irazu volcanoes. Total gaseous Hg was determined in samples collected at a height of 2 m using the Tekran 2537A (Tekran Inc.) gas-phase Hg vapor analyzer. Meteorological data (temperature, relative humidity, wind speed, wind direction, radiation and precipitation) were obtained from the airport weather station located at Alajuela. Monthly precipitation is typically 85 mm during the dry season (December to April) with winds from the west. The wet season begins in late April and continues to December with monthly rainfall of 328 mm and winds from the NE. The annual mean temperature is 20 deg. C

  16. Seasonal and diel patterns of total gaseous mercury concentration in the atmosphere of the Central Valley of Costa Rica

    Energy Technology Data Exchange (ETDEWEB)

    Castillo, Aylin; Valdes, Juan; Sibaja, Jose; Vega, Ilena; Alfaro, Rosa; Morales, Jose; Esquivel, Germain; Barrantes, Elisa [Laboratory for Atmospheric Chemistry, LAQAT-UNA, Universidad Nacional, P.O. Box 86-3000, Heredia (Costa Rica); Black, Paleah [Department of Biology, University of Ottawa, P.O. Box 450 Station A, Ottawa, Ontario, K1N 6N5 (Canada); Lean, David, E-mail: drslean@gmail.com [P.O. Box 309, Apsley, Ontario, K0L 1A0 (Canada)

    2011-02-15

    Research highlights: {yields} Elevated seasonal and daily patterns of total gaseous mercury (TGM) were observed in the Central Valley of Costa Rica 27 km south-east of the Poas volcano. {yields} With the onset of the wet season TGM in late April, values increased from typical values near 10 to 905 ng m{sup -3}. {yields} During the day, TGM values increased until midday along with temperature and radiation but relative humidity showed a reciprocal pattern. {yields} We conclude that elemental mercury from the volcano may react with atmospheric oxidants especially during the dry season and the mercury would be deposited to the ground. {yields} With the onset of heavy rains, mercury in the soil is reduced and re-volatilized resulting in the high levels in atmospheric air at the end of April. - Abstract: Monitoring of Hg in the atmosphere near volcanoes is limited with no previous data for Costa Rica. Seasonal and daily patterns of total gaseous mercury (TGM) were observed at the main sampling location at the Universidad Nacional, Heredia, Costa Rica. The area (lat. 10.000230 long. -84.109499) is located in the Central Valley of Costa Rica and is 27 km SE of the Poas volcano (lat. 10.199486 long. -84.231388). Measurements were made from May 2008 to May 2009 at this location with some additional values obtained at other sites near the Poas volcano including San Luis and Grecia as well as near, Turrialba and Irazu volcanoes. Total gaseous Hg was determined in samples collected at a height of 2 m using the Tekran 2537A (Tekran Inc.) gas-phase Hg vapor analyzer. Meteorological data (temperature, relative humidity, wind speed, wind direction, radiation and precipitation) were obtained from the airport weather station located at Alajuela. Monthly precipitation is typically 85 mm during the dry season (December to April) with winds from the west. The wet season begins in late April and continues to December with monthly rainfall of 328 mm and winds from the NE. The annual mean

  17. The ~ 2400-year cycle in atmospheric radiocarbon concentration: bispectrum of 14C data over the last 8000 years

    Directory of Open Access Journals (Sweden)

    S. S. Vasiliev

    2002-01-01

    Full Text Available We have carried out power spectrum, time-spectrum and bispectrum analyses of the long-term series of the radiocarbon concentrations deduced from measurements of the radiocarbon content in tree rings for the last 8000 years. Classical harmonic analysis of this time series shows a number of periods: 2400, 940, 710, 570, 500, 420, 360, 230, 210 and 190 years. A principle feature of the time series is the long period of ~ 2400 years, which is well known. The lines with periods of 710, 420 and 210 years are found to be the primary secular components of power spectrum. The complicated structure of the observed power spectrum is the result of ~ 2400-year modulation of primary secular components. The modulation induces the appearance of two side lines for every primary one, namely lines with periods of 940 and 570 years, of 500 and 360 years, and 230 and 190 years. The bispectral analysis shows that the parameters of carbon exchange system varied with the ~ 2400-year period during the last 8000 years. Variations of these parameters appear to be a climate effect on the rate of transfer of 14C between the atmosphere and the the ocean.Key words. Meteorology and atmospheric dynamics (climatology; ocean-atmosphere interaction; paleoclimatology

  18. The counteracting effects of elevated atmospheric CO2 concentrations and drought episodes: Studies of enchytraeid communities in a dry heathland

    DEFF Research Database (Denmark)

    Maraldo, Kristine; Krogh, Paul Henning; Linden, Leon

    2010-01-01

    The potential impacts of interactions of multiple climate change factors in soil ecosystems have received little attention. Most studies have addressed effects of single factors such as increased temperature or atmospheric CO2 but little is known about how such environmental factors will interact...... impact of drought on the enchytraeids, compared to the year with a wet summer and autumn (2007). Our study emphasises the importance of multi-factorial experimental design as a means to investigate effects of climatic changes.......The potential impacts of interactions of multiple climate change factors in soil ecosystems have received little attention. Most studies have addressed effects of single factors such as increased temperature or atmospheric CO2 but little is known about how such environmental factors will interact....... In the present study we investigate the effects of in situ exposure to elevated atmospheric CO2 concentration, increased temperatures and prolonged drought episodes on field communities of Enchytraeidae (Oligochaeta) in a dry heathland (Brandbjerg, Denmark). Increased CO2 had a positive effect on enchytraeid...

  19. 14 CFR Appendix B to Part 33 - Certification Standard Atmospheric Concentrations of Rain and Hail

    Science.gov (United States)

    2010-01-01

    ... fabricated from ice to simulate hail conditions, the use of water droplets and hail having shapes, sizes and distributions of sizes other than those defined in this appendix B, or the use of a single size or shape for... Concentrations Altitude (feet) Rain water content (RWC) (grams water/meter 3 air) 0 20.0 20,000 20.0 26,300 15.2...

  20. Atmospheric BTEX-concentrations in an area with intensive street traffic

    Science.gov (United States)

    Buczynska, Anna Jolanta; Krata, Agnieszka; Stranger, Marianne; Locateli Godoi, Ana Flavia; Kontozova-Deutsch, Velichka; Bencs, László; Naveau, Inge; Roekens, Edward; Van Grieken, René

    The major threat to clean air in developed and industrializing countries is now posed by traffic emissions. The effects of traffic road modifications on the air quality are, however, rarely reported in the literature. The aim of this study was to determine the influence of the modernization and renovation of a traffic artery in the region of Mortsel (Antwerp, Belgium) on the concentration of volatile organic compounds such as: benzene, toluene, ethylbenzene and m-, p-, o-xylenes (BTEX). The original goal of the reconstruction works was to reduce the traffic lanes of one of the busiest streets in Antwerp, in order to discourage the road traffic and in consequence also to improve the air quality in this region. The average concentrations of BTEX before these works in 2003 were: 1.6, 7.0, 0.9, 2.3, and 0.9 μg/m 3, for benzene, toluene, ethylbenzene, m + p xylenes, and o-xylene, respectively. However, after the completion of the works, in 2005, they were slightly higher: 2.5, 9.5, 1.6, 3.4, and 1.3 μg/m 3, respectively. The scatter plots of benzene against toluene, ethylbenzene and xylenes in 2003 and 2005 showed very good correlations. This fact indicated that all of the measured compounds originated from the same source, namely the road traffic. Moreover, the data obtained from an air-monitoring station at less than 6 km distance from the sampling site (operated by the Flemish Environment Agency, and located in Borgerhout, Antwerp), confirmed the lack of influence of background concentrations of BTEX. The obtained results led to the conclusion that the reduction of the number of traffic lanes had apparently increased the traffic jams and also increased the emission from cars. Therefore, these modernization works had even a negative impact on the local concentration of traffic-related pollutants as BTEX.

  1. An advanced analysis and modelling the air pollutant concentration temporal dynamics in atmosphere of the industrial cities: Odessa city

    Science.gov (United States)

    Buyadzhi, V. V.; Glushkov, A. V.; Khetselius, O. Yu; Ternovsky, V. B.; Serga, I. N.; Bykowszczenko, N.

    2017-10-01

    Results of analysis and modelling the air pollutant (dioxide of nitrogen) concentration temporal dynamics in atmosphere of the industrial city Odessa are presented for the first time and based on computing by nonlinear methods of the chaos and dynamical systems theories. A chaotic behaviour is discovered and investigated. To reconstruct the corresponding strange chaotic attractor, the time delay and embedding dimension are computed. The former is determined by the methods of autocorrelation function and average mutual information, and the latter is calculated by means of correlation dimension method and algorithm of false nearest neighbours. It is shown that low-dimensional chaos exists in the nitrogen dioxide concentration time series under investigation. Further, the Lyapunov’s exponents spectrum, Kaplan-Yorke dimension and Kolmogorov entropy are computed.

  2. Sudden increase in atmospheric concentration reveals strong coupling between shoot carbon uptake and root nutrient uptake in young walnut trees

    International Nuclear Information System (INIS)

    Delaire, M.; Sigogne, M.; Beaujard, F.; Frak, E.; Adam, B.; Le Roux, X.

    2005-01-01

    Short-term effects of a sudden increase in carbon dioxide concentration on nutrient uptake by roots during vegetative growth was studied in young walnut trees. Rates of carbon dioxide uptake and water loss by individual trees were determined by a branch bag method from three