Science.gov

Sample records for source emission rate

  1. Lidar method to estimate emission rates from extended sources

    USDA-ARS?s Scientific Manuscript database

    Currently, point measurements, often combined with models, are the primary means by which atmospheric emission rates are estimated from extended sources. However, these methods often fall short in their spatial and temporal resolution and accuracy. In recent years, lidar has emerged as a suitable to...

  2. Comparison of CALPUFF and ISCST3 models for predicting downwind odor and source emission rates

    NASA Astrophysics Data System (ADS)

    Wang, Lingjuan; Parker, David B.; Parnell, Calvin B.; Lacey, Ronald E.; Shaw, Bryan W.

    CALPUFF model and ISCST3 Gaussian dispersion models were evaluated for predicting downwind odor concentrations and back-calculating area source odor emission rates. The comparison between the predicted and field-sampled downwind concentrations indicates that the CALPUFF model could fairly well predict average downwind odor concentrations. However, ISCST3 tended to under predict downwind odor concentrations as compared to the measured concentrations. Both the CALPUFF and ISCST3 models failed to predict peak odor concentrations using the constant average emission rate. Odor emission rates obtained by back-calculating fluxes using CALPUFF and ISC models with the same field measurements of downwind odor concentrations are significantly different. It indicates that back-calculated emission rates are model specific. The modeled emission rates tended to be higher than flux chamber source sampling results. The flux chamber protocol may under-estimate odor emission rates.

  3. Comparison of odour emission rates measured from various sources using two sampling devices.

    PubMed

    Hudson, N; Ayoko, G A; Dunlop, M; Duperouzel, D; Burrell, D; Bell, K; Gallagher, E; Nicholas, P; Heinrich, N

    2009-01-01

    Two commonly used sampling devices (a wind tunnel and the US EPA dynamic emission chamber), were used to collect paired samples of odorous air from a number of agricultural odour sources. The odour samples were assessed using triangular, forced-choice dynamic olfactometry. The odour concentration data was combined with the flushing rate data to calculate odour emission rates for both devices on all sources. Odour concentrations were consistently higher in samples collected with a flux chamber (ratio ranging from 10:7 to 5:1, relative to wind tunnel samples), whereas odour emission rates were consistently larger when derived from wind tunnels (ratio ranging from 60:1 to 240:1, relative to flux chamber values). A complex relationship existed between emission rate estimates derived from each device, apparently influenced by the nature of the emitting surface. These results have great significance for users of odour dispersion models, for which an odour emission rate is a key input parameter.

  4. Odor emission rate estimation of indoor industrial sources using a modified inverse modeling method.

    PubMed

    Li, Xiang; Wang, Tingting; Sattayatewa, Chakkrid; Venkatesan, Dhesikan; Noll, Kenneth E; Pagilla, Krishna R; Moschandreas, Demetrios J

    2011-08-01

    Odor emission rates are commonly measured in the laboratory or occasionally estimated with inverse modeling techniques. A modified inverse modeling approach is used to estimate source emission rates inside of a postdigestion centrifuge building of a water reclamation plant. Conventionally, inverse modeling methods divide an indoor environment in zones on the basis of structural design and estimate source emission rates using models that assume homogeneous distribution of agent concentrations within a zone and experimentally determined link functions to simulate airflows among zones. The modified approach segregates zones as a function of agent distribution rather than building design and identifies near and far fields. Near-field agent concentrations do not satisfy the assumption of homogeneous odor concentrations; far-field concentrations satisfy this assumption and are the only ones used to estimate emission rates. The predictive ability of the modified inverse modeling approach was validated with measured emission rate values; the difference between corresponding estimated and measured odor emission rates is not statistically significant. Similarly, the difference between measured and estimated hydrogen sulfide emission rates is also not statistically significant. The modified inverse modeling approach is easy to perform because it uses odor and odorant field measurements instead of complex chamber emission rate measurements.

  5. Size-Resolved Source Emission Rates of Indoor Ultrafine Particles Considering Coagulation.

    PubMed

    Rim, Donghyun; Choi, Jung-Il; Wallace, Lance A

    2016-09-20

    Indoor ultrafine particles (UFP, <100 nm) released from combustion and consumer products lead to elevated human exposure to UFP. UFP emitted from the sources undergo aerosol transformation processes such as coagulation and deposition. The coagulation effect can be significant during the source emission due to high concentration and high mobility of nanosize particles. However, few studies have estimated size-resolved UFP source emission strengths while considering coagulation in their theoretical and experimental research work. The primary objective of this study is to characterize UFP source strength by considering coagulation in addition to other indoor processes (i.e., deposition and ventilation) in a realistic setting. A secondary objective is to test a hypothesis that size-resolved UFP source emission rates are unimodal and log-normally distributed for three common indoor UFP sources: an electric stove, a natural gas burner, and a paraffin wax candle. Experimental investigations were performed in a full-scale test building. Size- and time-resolved concentrations of UFP ranging from 2 to 100 nm were monitored using a scanning mobility particle sizer (SMPS). Based on the temporal evolution of the particle size distribution during the source emission period, the size-dependent source emission rate was determined using a material-balance modeling approach. The results indicate that, for a given UFP source, the source strength varies with particle size and source type. The analytical model assuming a log-normally distributed source emission rate could predict the temporal evolution of the particle size distribution with reasonable accuracy for the gas stove and the candle. Including the effect of coagulation was found to increase the estimates of source strengths by up to a factor of 8. This result implies that previous studies on indoor UFP source strengths considering only deposition and ventilation might have largely underestimated the true values of UFP source

  6. Inference of emission rates from multiple sources using Bayesian probability theory.

    PubMed

    Yee, Eugene; Flesch, Thomas K

    2010-03-01

    The determination of atmospheric emission rates from multiple sources using inversion (regularized least-squares or best-fit technique) is known to be very susceptible to measurement and model errors in the problem, rendering the solution unusable. In this paper, a new perspective is offered for this problem: namely, it is argued that the problem should be addressed as one of inference rather than inversion. Towards this objective, Bayesian probability theory is used to estimate the emission rates from multiple sources. The posterior probability distribution for the emission rates is derived, accounting fully for the measurement errors in the concentration data and the model errors in the dispersion model used to interpret the data. The Bayesian inferential methodology for emission rate recovery is validated against real dispersion data, obtained from a field experiment involving various source-sensor geometries (scenarios) consisting of four synthetic area sources and eight concentration sensors. The recovery of discrete emission rates from three different scenarios obtained using Bayesian inference and singular value decomposition inversion are compared and contrasted.

  7. Air pollutant emission rates for sources at the Deaf Smith County repository site

    SciTech Connect

    Not Available

    1985-11-01

    This document summarizes the air-quality source terms used for the Deaf Smith County, Texas environmental assessment report and explains their derivation. The engineering data supporting these source terms appear as appendixes to this report and include summary equipment lists for the repository and detailed equipment lists for the exploratory shaft. Although substantial work has been performed in establishing the current repository design, a greater effort will be required for the final design. Consequently, the repository emission rates presented here should be considered as preliminary estimates. Another set of air pollution emission rates will be calculated after design data are more firmly established. 18 refs., 15 tabs.

  8. Odor sampling: techniques and strategies for the estimation of odor emission rates from different source types.

    PubMed

    Capelli, Laura; Sironi, Selena; Del Rosso, Renato

    2013-01-15

    Sampling is one of the main issues pertaining to odor characterization and measurement. The aim of sampling is to obtain representative information on the typical characteristics of an odor source by means of the collection of a suitable volume fraction of the effluent. The most important information about an emission source for odor impact assessment is the so-called Odor Emission Rate (OER), which represents the quantity of odor emitted per unit of time, and is expressed in odor units per second (ou∙s-1). This paper reviews the different odor sampling strategies adopted depending on source type. The review includes an overview of odor sampling regulations and a detailed discussion of the equipment to be used as well as the mathematical considerations to be applied to obtain the OER in relation to the sampled source typology.

  9. Odor Sampling: Techniques and Strategies for the Estimation of Odor Emission Rates from Different Source Types

    PubMed Central

    Capelli, Laura; Sironi, Selena; Rosso, Renato Del

    2013-01-01

    Sampling is one of the main issues pertaining to odor characterization and measurement. The aim of sampling is to obtain representative information on the typical characteristics of an odor source by means of the collection of a suitable volume fraction of the effluent. The most important information about an emission source for odor impact assessment is the so-called Odor Emission Rate (OER), which represents the quantity of odor emitted per unit of time, and is expressed in odor units per second (ou·s−1). This paper reviews the different odor sampling strategies adopted depending on source type. The review includes an overview of odor sampling regulations and a detailed discussion of the equipment to be used as well as the mathematical considerations to be applied to obtain the OER in relation to the sampled source typology. PMID:23322098

  10. GAS-PHASE MASS TRANSFER MODEL FOR PREDICTING VOLATILE ORGANIC COMPOUND (VOC) EMISSION RATES FROM INDOOR POLLUTANT SOURCES

    EPA Science Inventory

    Analysis of the impact of sources on indoor pollutant concentrations and occupant exposure to indoor pollutants requires knowledge of the emission rates from the sources. Emission rates are often determined by chamber testing and the data from the chamber test are fitted to an em...

  11. GAS-PHASE MASS TRANSFER MODEL FOR PREDICTING VOLATILE ORGANIC COMPOUND (VOC) EMISSION RATES FROM INDOOR POLLUTANT SOURCES

    EPA Science Inventory

    Analysis of the impact of sources on indoor pollutant concentrations and occupant exposure to indoor pollutants requires knowledge of the emission rates from the sources. Emission rates are often determined by chamber testing and the data from the chamber test are fitted to an em...

  12. Observed Barium Emission Rates

    NASA Technical Reports Server (NTRS)

    Stenbaek-Nielsen, H. C.; Wescott, E. M.; Hallinan, T. J.

    1993-01-01

    The barium releases from the CRRES satellite have provided an opportunity for verifying theoretically calculated barium ion and neutral emission rates. Spectra of the five Caribbean releases in the summer of 1991 were taken with a spectrograph on board a U.S. Air Force jet aircraft. Because the line of sight release densities are not known, only relative rates could be obtained. The observed relative rates agree well with the theoretically calculated rates and, together with other observations, confirm the earlier detailed theoretical emission rates. The calculated emission rates can thus with good accuracy be used with photometric observations. It has been postulated that charge exchange between neutral barium and oxygen ions represents a significant source for ionization. If so. it should be associated with emissions at 4957.15 A and 5013.00 A, but these emissions were not detected.

  13. Evaluation of emission rates and observation of natural sources of nitrogen oxides in acid rain area of southern China

    SciTech Connect

    Miao-Qin Lu; Yu-Bao Wang

    1996-12-31

    The present paper reports the observation results of natural sources of NO, N{sub 2}O, NO{sub 2} in the area of Fujien province, southeast of China, where acidic rain occurs at relatively high frequency. The emission rates of NO, N{sub 2}O, NO{sub 2} in paddy field and dry farmland in Xiamen, Jimei district, Tongan and Guoan counties were measured in this investigation. The measurement results shows that the emission rates of nitrogen oxides from paddy field are higher than that from dry farmland. The emission rate of NO{sub 2} was the highest among the three nitrogen oxides. But no more difference between NO and N{sub 2}O. It should be noted that the emission rates of nitrogen oxides from paddy field in Jimei area are obviously higher than that in Tongan. The main reason for this difference resulted from the different types of soils between those two areas.

  14. Optimizing the Point-Source Emission Rates and Geometries of Pheromone Mating Disruption Mega-Dispensers.

    PubMed

    Baker, T C; Myrick, A J; Park, K C

    2016-09-01

    High-emission-rate "mega-dispensers" have come into increasing use for sex pheromone mating disruption of moth pests over the past two decades. These commercially available dispensers successfully suppress mating and reduce crop damage when they are deployed at very low to moderate densities, ranging from 1 to 5/ha to 100-1000/ha, depending on the dispenser types and their corresponding pheromone emission rates. Whereas traditionally the emission rates for successful commercial mating disruption formulations have been measured in terms of amounts (usually milligram) emitted by the disruptant application per acre or hectare per day, we suggest that emission rates should be measured on a per-dispenser per-minute basis. In addition we suggest, because of our knowledge concerning upwind flight of male moths being dependent on contact with pheromone plume strands, that more attention needs to be paid to optimizing the flux within plume strands that shear off of any mating disruption dispenser's surface. By measuring the emission rates on a per-minute basis and measuring the plume strand concentrations emanating from the dispensers, it may help improve the ability of the dispensers to initiate upwind flight from males and initiate their habituation to the pheromone farther downwind than can otherwise be achieved. In addition, by optimizing plume strand flux by paying attention to the geometries and compactness of mating disruption mega-dispensers may help reduce the cost of mega-dispenser disruption formulations by improving their behavioral efficacy while maintaining field longevity and using lower loading rates per dispenser.

  15. Estimation of point source fugitive emission rates from a single sensor time series: a conditionally-sampled Gaussian plume reconstruction

    EPA Science Inventory

    This paper presents a technique for determining the trace gas emission rate from a point source. The technique was tested using data from controlled methane release experiments and from measurement downwind of a natural gas production facility in Wyoming. Concentration measuremen...

  16. Bayesian Estimation of Fugitive Methane Point Source Emission Rates from a SingleDownwind High-Frequency Gas Sensor

    EPA Science Inventory

    Bayesian Estimation of Fugitive Methane Point Source Emission Rates from a Single Downwind High-Frequency Gas Sensor With the tremendous advances in onshore oil and gas exploration and production (E&P) capability comes the realization that new tools are needed to support env...

  17. Estimation of point source fugitive emission rates from a single sensor time series: a conditionally-sampled Gaussian plume reconstruction

    EPA Science Inventory

    This paper presents a technique for determining the trace gas emission rate from a point source. The technique was tested using data from controlled methane release experiments and from measurement downwind of a natural gas production facility in Wyoming. Concentration measuremen...

  18. Bayesian Estimation of Fugitive Methane Point Source Emission Rates from a SingleDownwind High-Frequency Gas Sensor

    EPA Science Inventory

    Bayesian Estimation of Fugitive Methane Point Source Emission Rates from a Single Downwind High-Frequency Gas Sensor With the tremendous advances in onshore oil and gas exploration and production (E&P) capability comes the realization that new tools are needed to support env...

  19. Quantification of Greenhouse Gas Emission Rates from strong Point Sources by Airborne IPDA-Lidar Measurements: Methodology and Experimental Results

    NASA Astrophysics Data System (ADS)

    Ehret, G.; Amediek, A.; Wirth, M.; Fix, A.; Kiemle, C.; Quatrevalet, M.

    2016-12-01

    We report on a new method and on the first demonstration to quantify emission rates from strong greenhouse gas (GHG) point sources using airborne Integrated Path Differential Absorption (IPDA) Lidar measurements. In order to build trust in the self-reported emission rates by countries, verification against independent monitoring systems is a prerequisite to check the reported budget. A significant fraction of the total anthropogenic emission of CO2 and CH4 originates from localized strong point sources of large energy production sites or landfills. Both are not monitored with sufficiently accuracy by the current observation system. There is a debate whether airborne remote sensing could fill in the gap to infer those emission rates from budgeting or from Gaussian plume inversion approaches, whereby measurements of the GHG column abundance beneath the aircraft can be used to constrain inverse models. In contrast to passive sensors, the use of an active instrument like CHARM-F for such emission verification measurements is new. CHARM-F is a new airborne IPDA-Lidar devised for the German research aircraft HALO for the simultaneous measurement of the column-integrated dry-air mixing ratio of CO2 and CH4 commonly denoted as XCO2 und XCH4, respectively. It has successfully been tested in a serious of flights over Central Europe to assess its performance under various reflectivity conditions and in a strongly varying topography like the Alps. The analysis of a methane plume measured in crosswind direction of a coal mine ventilation shaft revealed an instantaneous emission rate of 9.9 ± 1.7 kt CH4 yr-1. We discuss the methodology of our point source estimation approach and give an outlook on the CoMet field experiment scheduled in 2017 for the measurement of anthropogenic and natural GHG emissions by a combination of active and passive remote sensing instruments on research aircraft.

  20. Measurement of the emission rate of an aerosol source--comparison of aerosol and gas transport coefficients.

    PubMed

    Bémer, D; Callé, S; Godinot, S; Régnier, R; Dessagne, J M

    2000-12-01

    A measuring method of the emission rate of an atmospheric pollutant source, based on the use of a tracer gas (helium) and developed in the case of a gaseous source, was tested for an aerosol source. The influence of both particle sedimentation and wall depositions was studied. The transport coefficients of the tracer gas and of alumina particles of various particle sizes (MMAD from 8 to 36 microns) were measured on a vertical axis close to the source, in a 71 m3 room swept by a piston flow. The measurements clearly demonstrated the predominant influence of sedimentation in the case of particles with aerodynamic diameters greater than 10 microns. Particle wall deposition was determined by measuring the gas and particle concentration decay in the ventilated room. To do this, a new tracing method using a fluorescent aerosol was developed. The measured aerosol deposition rates are much higher than those calculated from the formula of Corner for a cubical volume. Aerosol sedimentation and wall deposition are two phenomena limiting the use of a tracer gas to measure the aerosol emission rate. The chemical substances and materials used in work premises are likely to be released into the atmosphere and lead to the formation of pollutants. These emissions stem from either physical or chemical processes (evaporation of a solvent) or from mechanical processes (dispersion of oil droplets at the source of mists).

  1. Analysis of available ambient and stationary source HAP sampling results to verify emission rate estimates for sources in Ambos Nogales

    SciTech Connect

    Powers, B.; Fernandez, C.; Oliver, B.; Dickson, R.

    1996-12-31

    The Arizona Department of Environmental Quality (ADEQ) is funding a project to develop comprehensive hazardous air pollutant (HAP) emissions inventories for the cross-border communities of Nogales, Arizona and Nogales, Sonora, Mexico. Ambient VOC and PAH data were collected in downtown Nogales, Sonora in July 1994 by the ADEQ. This paper addresses the analysis of the ambient HAP data performed by the project team. The ambient HAP data evaluation will serve as a cross-check of the accuracy of the RAP emission estimates developed for each source type included in the HAP emissions inventory. The data show that benzene, toluene, xylene, ethylbenzene (BTXE) and aldehydes are the dominant volatile organic compound (VOC) HAPs in the ambient air. The quantity of BTXE in the ambient air, and ratio of these compounds to each other, implies that mobile sources are the principal source of BTXE in Nogales, Sonora. Significant levels of olefinic VOCs were also detected. Ambient test data also indicate ethane, propane, butane, pentane are the predominant VOC species in the ambient air. Liquified petroleum gas (LPG) cylinders are the probable source of these VOCs. Almost all residential and commercial cooking performed in Nogales, Sonora is done from LPG cylinders containing a mixture of propane (primarily) and butane. These cylinders are ubiquitous, and many are equipped with potentially leaky valves. VOC and VOC HAP test protocols are currently being developed by the Mexican National Institute of Ecology for these cylinders and associated cooking ranges. Periodic open burning of municipal solid waste (MSW) is performed at a site located on the border in Nogales, Sonora. Ambient VOC HAP data collected in July 1994 during both MSW burning periods and {open_quotes}no burn{close_quotes} periods is being evaluated to determine if the contribution of open burning to the ambient HAP burden can be estimated for both particulate and VOC HAPs from the ambient data. 7 refs.

  2. Emission rates of benzene and ammonia area sources determined by spectroscopic remote measurements and inverse dispersion modeling

    NASA Astrophysics Data System (ADS)

    Schaefer, Klaus; Emeis, Stefan M.; Stockhause, Martina; Sedlmaier, Achim; Hoffmann, Herbert; Depta, Georg; Gronauer, Andreas

    1999-02-01

    The emission rates of diffuse and heterogeneous distributed sources are difficult to determine because point measurements are not representative. Therefore a method was further developed to determine gaseous emission rates by measurements of path-integrated mixing ratios with open-path spectroscopic systems in the exhaust plume (VOC, NH3, CH4, N2O, CO, CO2) and of meteorological parameters. Inverse dispersion modeling is used to quantify the emission rates afterwards with these data. The measurements are performed by Fourier Transform Infrared (FTIR) spectroscopy and Differential Optical Absorption Spectroscopy (DOAS) at 50 to 500 m optical path lengths about 1 to 20 m above ground level. The measurement accuracy for greenhouse gases and ammonia is about plus or minus 10% and for BTX about plus or minus 30%. The whole method was validated at a livestock building with a single exhaust chimney. The Gaussian model PAL was applied for inverse modeling to investigate limited pieces of land and isolated facilities in flat terrain. Including the accuracy of the dispersion simulations the determined emission rates have an error margin of about plus or minus 30%. Results of measurement campaigns are discussed as emission rates of ammonia from slurry spreading as well as of benzene from gas stations and a tank farm.

  3. Biogenic Emission Sources

    EPA Pesticide Factsheets

    Biogenic emissions sources come from natural sources and need to accounted for in photochemical grid models. They are computed using a model which utilizes spatial information on vegetation and land use.

  4. A primary standard for the measurement of alpha and beta particle surface emission rate from large area reference sources.

    PubMed

    Ravindra, Anuradha; Kulkarni, D B; Joseph, Leena; Kulkarni, M S; Babu, D A R

    2016-01-01

    A large area windowless gas flow multi wire proportional counting system for the calibration of large area reference sources has been developed as a primary standard at Bhabha Atomic Research Centre (BARC). The counting system consists of a multi wire proportional counter (MWPC), vacuum system, gas flow system and pulse processing units. The MWPC detector assembly consists of a vacuum tight aluminum enclosure, multi wire grid and sliding source tray. Various detector characteristics like operating characteristics curve, Fe-55 spectrum for beta discriminator threshold setting and dead time of the measurement system were studied and determined in order to achieve an optimized detection capability. The surface emission rates of different source strengths were measured and their relative combined standard uncertainties were determined. Large Area Sources Comparison Exercise (LASCE) was organized by International Committee on Radionuclide Metrology (ICRM) working group and coordinated by National Institute for Ionising Radiation Metrology (ENEA), Italy, to demonstrate equivalence of surface emission rate measurements at the international platform. BARC participated in the programme and the results of LASCE are also discussed in this paper. Copyright © 2015 Elsevier Ltd. All rights reserved.

  5. Volatile organic compound concentrations, emission rates, and source apportionment in newly-built apartments at pre-occupancy stage.

    PubMed

    Shin, Seung H; Jo, Wan K

    2012-10-01

    The present study investigated the indoor concentrations of selected volatile organic compounds (VOCs) and formaldehyde and their indoor emission characteristics in newly-built apartments at the pre-occupancy stage. In total, 107 apartments were surveyed for indoor and outdoor VOC concentrations in two metropolitan cities and one rural area in Korea. A mass balanced model was used to estimate surface area-specific emission rates of individual VOCs and formaldehyde. Seven (benzene, ethyl benzene, toluene, m,p-xylene, o-xylene, n-hexane, and n-heptane) of 40 target compounds were detectable in all indoor air samples, whereas the first five were detected in all outdoor air samples. Formaldehyde was also predominant in the indoor air samples, with a high detection frequency of 96%. The indoor concentrations were significantly higher than the outdoor concentrations for aromatics, alcohols, terpenes, and ketones. However, six halogenated VOCs exhibited similar concentrations for indoor and outdoor air samples, suggesting that they are not major components emitted from building materials. It was also suggested that a certain portion of the apartments surveyed were constructed by not following the Korean Ministry of Environment guidelines for formaldehyde emissions. Toluene exhibited the highest emission rate with a median value of 138 μg m(-2) h(-1). The target compounds with median emission rates greater than 20 μg m(-2) h(-1) were toluene, 1-propanol, formaldehyde, and 2-butanone. The wood panels/vinyl floor coverings were the largest indoor pollutant source, followed by floorings, wall coverings, adhesives, and paints. The wood panels/vinyl floor coverings contributed nearly three times more to indoor VOC concentrations than paints. Copyright © 2012 Elsevier Ltd. All rights reserved.

  6. Field emission electron source

    DOEpatents

    Zettl, Alexander Karlwalter; Cohen, Marvin Lou

    2000-01-01

    A novel field emitter material, field emission electron source, and commercially feasible fabrication method is described. The inventive field emission electron source produces reliable electron currents of up to 400 mA/cm.sup.2 at 200 volts. The emitter is robust and the current it produces is not sensitive to variability of vacuum or the distance between the emitter tip and the cathode. The novel emitter has a sharp turn-on near 100 volts.

  7. The content of 250Cf and 248Cm in 252Cf neutron sources and the effect on the neutron emission rate.

    PubMed

    Roberts, N J; Jones, L N

    2007-01-01

    One of the most common radionuclide neutron sources used for the calibration of detectors is (252)Cf. However, these sources also contain (250)Cf, which is present in the material from which the sources are made, and (248)Cm, which is formed as the daughter of (252)Cf via alpha-decay. Both decay by spontaneous fission with longer half-lives than (252)Cf. Consequently, as the source becomes older, the emission rate does not follow the decay curve of (252)Cf. Fits have been made to emission rate measurements of (252)Cf sources at NPL spanning over 30 y to deduce their (250)Cf and (248)Cm content. The emission rate of a source can be significantly underestimated if the presence of (250)Cf and (248)Cm is not taken into account, and this has been investigated for a typical (252)Cf source. The importance of this problem to other calibration laboratories and users of (252)Cf sources is emphasised.

  8. Global Scale Attribution of Anthropogenic and Natural Dust Sources and their Emission Rates Based on MODIS Deep Blue Aerosol Products

    NASA Technical Reports Server (NTRS)

    Ginoux, Paul; Prospero, Joseph M.; Gill, Thomas E.; Hsu, N. Christina; Zhao, Ming

    2012-01-01

    Our understanding of the global dust cycle is limited by a dearth of information about dust sources, especially small-scale features which could account for a large fraction of global emissions. Here we present a global-scale high-resolution (0.1 deg) mapping of sources based on Moderate Resolution Imaging Spectroradiometer (MODIS) Deep Blue estimates of dust optical depth in conjunction with other data sets including land use. We ascribe dust sources to natural and anthropogenic (primarily agricultural) origins, calculate their respective contributions to emissions, and extensively compare these products against literature. Natural dust sources globally account for 75% of emissions; anthropogenic sources account for 25%. North Africa accounts for 55% of global dust emissions with only 8% being anthropogenic, mostly from the Sahel. Elsewhere, anthropogenic dust emissions can be much higher (75% in Australia). Hydrologic dust sources (e.g., ephemeral water bodies) account for 31% worldwide; 15% of them are natural while 85% are anthropogenic. Globally, 20% of emissions are from vegetated surfaces, primarily desert shrublands and agricultural lands. Since anthropogenic dust sources are associated with land use and ephemeral water bodies, both in turn linked to the hydrological cycle, their emissions are affected by climate variability. Such changes in dust emissions can impact climate, air quality, and human health. Improved dust emission estimates will require a better mapping of threshold wind velocities, vegetation dynamics, and surface conditions (soil moisture and land use) especially in the sensitive regions identified here, as well as improved ability to address small-scale convective processes producing dust via cold pool (haboob) events frequent in monsoon regimes.

  9. Assessment and Optimization of the Accuracy of an Aircraft-Based Technique Used to Quantify Greenhouse Gas Emission Rates from Point Sources

    NASA Astrophysics Data System (ADS)

    Shepson, P. B.; Lavoie, T. N.; Kerlo, A. E.; Stirm, B. H.

    2016-12-01

    Understanding the contribution of anthropogenic activities to atmospheric greenhouse gas concentrations requires an accurate characterization of emission sources. Previously, we have reported the use of a novel aircraft-based mass balance measurement technique to quantify greenhouse gas emission rates from point and area sources, however, the accuracy of this approach has not been evaluated to date. Here, an assessment of method accuracy and precision was performed by conducting a series of six aircraft-based mass balance experiments at a power plant in southern Indiana and comparing the calculated CO2 emission rates to the reported hourly emission measurements made by continuous emissions monitoring systems (CEMS) installed directly in the exhaust stacks at the facility. For all flights, CO2 emissions were quantified before CEMS data were released online to ensure unbiased analysis. Additionally, we assess the uncertainties introduced to the final emission rate caused by our analysis method, which employs a statistical kriging model to interpolate and extrapolate the CO2 fluxes across the flight transects from the ground to the top of the boundary layer. Subsequently, using the results from these flights combined with the known emissions reported by the CEMS, we perform an inter-model comparison of alternative kriging methods to evaluate the performance of the kriging approach.

  10. Exploiting dual otoacoustic emission sources

    NASA Astrophysics Data System (ADS)

    Abdala, Carolina; Kalluri, Radha

    2015-12-01

    Two distinct processes generate otoacoustic emissions (OAEs). Reflection-source emissions, here recorded as stimulus frequency OAEs, are optimally informative at low sound levels and are more sensitive to slight hearing loss; they have been linked to cochlear amplifier gain and tuning. Distortion-source emissions are strongest at moderate-high sound levels and persist despite mild hearing loss; they likely originate in the nonlinear process of hair cell transduction. In this preliminary study, we exploit the unique features of each by generating a combined reflection-distortion OAE profile in normal hearing and hearing-impaired ears. Distortion-product (DP) and stimulus-frequency (SF) OAEs were recorded over a broad range of stimulus levels and frequencies. Individual I/O and transfer functions were generated for both emission types in each ear, and OAE peak strength, compression threshold, and rate of compression were calculated. These combined SFOAE and DPOAE features in normal and hearing-impaired ears may provide a potentially informative and novel index of hearing loss. This is an initial step toward utilizing OAE source in characterizing cochlear function and dysfunction.

  11. Minimization of nitrous oxide emission from CASS process treating low carbon source domestic wastewater: Effect of feeding strategy and aeration rate.

    PubMed

    Liang, Weihao; Yu, Chao; Ren, Hongqiang; Geng, Jinju; Ding, Lili; Xu, Ke

    2015-12-01

    Nitrous oxide (N2O) emission during wastewater treatment can be mitigated by improving operational conditions, e.g., organic carbon supply and dissolved oxygen. To evaluate the control parameters for N2O emission in the low carbon source domestic wastewater treatment process, N2O emissions from Cyclic Activated Sludge System (CASS) under different feeding strategies and aeration rates were investigated. Results showed that continuous feeding enhanced nitrogen removal and reduced N2O emission compared to batch feeding, while a higher aeration rate led to less N2O emission. N2O was mainly produced during non-aeration phases in batch feeding CASS and the amount of N2O generated from denitrification decreased under continuous feeding, indicating that carbon source in the continuous influent relieved the electron competition between denitrification reductases during non-aeration phase. Moreover, taxonomic analysis based on high-throughput 16S rRNA gene sequencing revealed higher abundance of denitrifying bacteria, especially N2O-reducing bacteria in continuous feeding CASS.

  12. VOCs emission rate estimate for complicated industrial area source using an inverse-dispersion calculation method: A case study on a petroleum refinery in Northern China.

    PubMed

    Wei, Wei; Lv, Zhaofeng; Yang, Gan; Cheng, Shuiyuan; Li, Yue; Wang, Litao

    2016-11-01

    This study aimed to apply an inverse-dispersion calculation method (IDM) to estimate the emission rate of volatile organic compounds (VOCs) for the complicated industrial area sources, through a case study on a petroleum refinery in Northern China. The IDM was composed of on-site monitoring of ambient VOCs concentrations and meteorological parameters around the source, calculation of the relationship coefficient γ between the source's emission rate and the ambient VOCs concentration by the ISC3 model, and estimation of the actual VOCs emission rate from the source. Targeting the studied refinery, 10 tests and 8 tests were respectively conducted in March and in June of 2014. The monitoring showed large differences in VOCs concentrations between background and downwind receptors, reaching 59.7 ppbv in March and 248.6 ppbv in June, on average. The VOCs increases at receptors mainly consisted of ethane (3.1%-22.6%), propane (3.8%-11.3%), isobutane (8.5%-10.2%), n-butane (9.9%-13.2%), isopentane (6.1%-12.9%), n-pentane (5.1%-9.7%), propylene (6.1-11.1%) and 1-butylene (1.6%-5.4%). The chemical composition of the VOCs increases in this field monitoring was similar to that of VOCs emissions from China's refineries reported, which revealed that the ambient VOCs increases were predominantly contributed by this refinery. So, we used the ISC3 model to create the relationship coefficient γ for each receptor of each test. In result, the monthly VOCs emissions from this refinery were calculated to be 183.5 ± 89.0 ton in March and 538.3 ± 281.0 ton in June. The estimate in June was greatly higher than in March, chiefly because the higher environmental temperature in summer produced more VOCs emissions from evaporation and fugitive process of the refinery. Finally, the VOCs emission factors (g VOCs/kg crude oil refined) of 0.73 ± 0.34 (in March) and 2.15 ± 1.12 (in June) were deduced for this refinery, being in the same order with previous direct

  13. Measuring the emission rate of an aerosol source placed in a ventilated room using a tracer gas: influence of particle wall deposition.

    PubMed

    Bémer, D; Lecler, M T; Régnier, R; Hecht, G; Gerber, J M

    2002-04-01

    A method to measure the emission rate of an airborne pollutant source using a tracer gas was tested in the case of an aerosol source. The influence of particle deposition on the walls of a test room of 72 m3 was studied. The deposition rate of an aerosol of MgCl2 was determined by means of two methods: one based on measuring the aerosol concentration decay inside the ventilated room, the other based on calculation of the material mass balance. The concentration decay was monitored by optical counting and the aerosol mass concentration determined by means of sampling on a filter and analysis of the mass deposited by atomic absorption spectrometry. Four series of measurements were carried out. The curve giving the deposition rate according to the particle aerodynamic diameter (d(ae)) was established and shows deposition rates higher than those predicted using the model of Corner. The decay method gives the best results. The study carried out has shown that the phenomenon of deposition has little effect on the measurement of the aerosol source emission rate using a tracer gas for particles of aerodynamic diameter < 5 microm (underestimation < 25%). For particles of a greater diameter, wall deposition is an extremely limiting factor for the method, the influence of which can, however, be limited by using a test booth of small volume and keeping the sampling duration as short as possible.

  14. Acoustic emission source location

    NASA Astrophysics Data System (ADS)

    Promboon, Yajai

    The objective of the research program was development of reliable source location techniques. The study comprised two phases. First, the research focused on development of source location methods for homogeneous plates. The specimens used in the program were steel railroad tank cars. Source location methods were developed and demonstrated for empty and water filled tanks. The second phase of the research was an exploratory study of source location method for fiber reinforced composites. Theoretical analysis and experimental measurement of wave propagation were carried out. This data provided the basis for development of a method using the intersection of the group velocity curves for the first three wave propagation modes. Simplex optimization was used to calculate the location of the source. Additional source location methods have been investigated and critically examined. Emphasis has been placed on evaluating different methods for determining the time of arrival of a wave. The behavior of wave in a water filled tank was studied and source location methods suitable for use in this situation have been examined through experiment and theory. Particular attention is paid to the problem caused by leaky Lamb waves. A preliminary study into the use of neural networks for source location in fiber reinforced composites was included in the research program. A preliminary neural network model and the results from training and testing data are reported.

  15. Long term observations of halogenated greenhouse gases in a European continental background station for assessing atmospheric trends, annual growth rates and emission sources

    NASA Astrophysics Data System (ADS)

    Maione, M.; Arduini, J.; Uguccioni, F.; Giostra, U.; Furlani, F.; Belfiore, L.; Cava, D.

    2009-04-01

    Climate altering halocarbons are continuously monitored at the atmospheric research station "O. Vittori" located on the top of Monte Cimone, Northern Apennines, Italy ( 2165 m asl), in the frame of the SOGE (System for Observation of halogenated Greenhouse gases in Europe) network, an integrated system based on a combination of observations and models aimed at assessing atmospheric trends, annual growth rates and at estimating European halocarbon emissions. The use of such a top-down approach is useful to ascertain compliance to International Protocols regulating production/emission of halogenated greenhouse gases. Establishing the baseline is essential both for estimating annual growth rates and because back attribution techniques are based on the clear identification of "above the background" data. That is particularly challenging in a Station like Monte Cimone characterised by a complex meteorological and source field. The approach proposed is based on the identification of the lowest concentration values in a given temporal range to which a ∆c representing variation due to instrumental error is added. Trends are evaluated by using a non-linear regression function, able to take into account both annual and seasonal variation. In order to identify source, regions baseline data are subtracted from the full data set and an inversion modelling cascade, which makes use of MM5 model to reproduce meteorological fields and of FLEXPART to simulate tracer dispersion, is used to find the best emissions map that fits the observations.

  16. International key comparison of measurements of neutron source emission rate (1999-2005): CCRI(III)-K9.AmBe

    NASA Astrophysics Data System (ADS)

    Roberts, N. J.; Jones, L. N.; Wang, Z.; Liu, Y.; Wang, Q.; Chen, X.; Luo, H.; Rong, C.; Králik, M.; Park, H.; Choi, K. O.; Pereira, W. W.; da Fonseca, E. S.; Cassette, P.; Dewey, M. S.; Moiseev, N. N.; Kharitonov, I. A.

    2011-01-01

    Section III (neutron measurements) of the Comité Consultatif des Rayonnements Ionisants, CCRI, conducted a key comparison of primary measurements of the neutron emission rate of an 241Am-Be(α,n) radionuclide source. A single 241Am-Be(α,n) source was circulated to all the participants between 1999 and 2005. Eight laboratories participated—the CIAE (China), CMI (Czech Republic), KRISS (Republic of Korea), LNMRI (Brazil), LNE-LNHB (France), NIST (USA), NPL (UK) and the VNIIM (Russian Federation)—with the NPL making their measurements at the start and repeating them near the end of the exercise to verify the stability of the source. Each laboratory reported the emission rate into 4π sr together with a detailed uncertainty budget. All participants used the manganese bath technique, with the VNIIM also making measurements using an associated particle technique. The CMI, KRISS, VNIIM, and later the NPL, also measured the anisotropy of the source although this was not a formal part of the comparison. The first draft report was released in May 2006 and having been discussed and modified by the participants and subsequently reviewed by the CCRI(III), the present paper is now the final report of the comparison. Main text. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the CCRI Section III, according to the provisions of the CIPM Mutual Recognition Arrangement (MRA).

  17. MAMAP - a new spectrometer system for column-averaged methane and carbon dioxide observations from aircraft: retrieval algorithm and first inversions for point source emission rates

    NASA Astrophysics Data System (ADS)

    Krings, T.; Gerilowski, K.; Buchwitz, M.; Reuter, M.; Tretner, A.; Erzinger, J.; Heinze, D.; Burrows, J. P.; Bovensmann, H.

    2011-04-01

    MAMAP is an airborne passive remote sensing instrument designed for measuring columns of methane (CH4) and carbon dioxide (CO2). The MAMAP instrument consists of two optical grating spectrometers: One in the short wave infrared band (SWIR) at 1590-1690 nm to measure CO2 and CH4 absorptions and another one in the near infrared (NIR) at 757-768 nm to measure O2 absorptions for reference purposes. MAMAP can be operated in both nadir and zenith geometry during the flight. Mounted on an airplane MAMAP can effectively survey areas on regional to local scales with a ground pixel resolution of about 29 m × 33 m for a typical aircraft altitude of 1250 m and a velocity of 200 km h-1. The retrieval precision of the measured column relative to background is typically ≲ 1% (1σ). MAMAP can be used to close the gap between satellite data exhibiting global coverage but with a rather coarse resolution on the one hand and highly accurate in situ measurements with sparse coverage on the other hand. In July 2007 test flights were performed over two coal-fired powerplants operated by Vattenfall Europe Generation AG: Jänschwalde (27.4 Mt CO2 yr-1) and Schwarze Pumpe (11.9 Mt CO2 yr-1), about 100 km southeast of Berlin, Germany. By using two different inversion approaches, one based on an optimal estimation scheme to fit Gaussian plume models from multiple sources to the data, and another using a simple Gaussian integral method, the emission rates can be determined and compared with emissions as stated by Vattenfall Europe. An extensive error analysis for the retrieval's dry column results (XCO2 and XCH4) and for the two inversion methods has been performed. Both methods - the Gaussian plume model fit and the Gaussian integral method - are capable of delivering reliable estimates for strong point source emission rates, given appropriate flight patterns and detailed knowledge of wind conditions.

  18. Global-scale attribution of anthropogenic and natural dust sources and their emission rates based on MODIS Deep Blue aerosol products

    NASA Astrophysics Data System (ADS)

    Ginoux, Paul; Prospero, Joseph M.; Gill, Thomas E.; Hsu, N. Christina; Zhao, Ming

    2012-09-01

    Our understanding of the global dust cycle is limited by a dearth of information about dust sources, especially small-scale features which could account for a large fraction of global emissions. Here we present a global-scale high-resolution (0.1°) mapping of sources based on Moderate Resolution Imaging Spectroradiometer (MODIS) Deep Blue estimates of dust optical depth in conjunction with other data sets including land use. We ascribe dust sources to natural and anthropogenic (primarily agricultural) origins, calculate their respective contributions to emissions, and extensively compare these products against literature. Natural dust sources globally account for 75% of emissions; anthropogenic sources account for 25%. North Africa accounts for 55% of global dust emissions with only 8% being anthropogenic, mostly from the Sahel. Elsewhere, anthropogenic dust emissions can be much higher (75% in Australia). Hydrologic dust sources (e.g., ephemeral water bodies) account for 31% worldwide; 15% of them are natural while 85% are anthropogenic. Globally, 20% of emissions are from vegetated surfaces, primarily desert shrublands and agricultural lands. Since anthropogenic dust sources are associated with land use and ephemeral water bodies, both in turn linked to the hydrological cycle, their emissions are affected by climate variability. Such changes in dust emissions can impact climate, air quality, and human health. Improved dust emission estimates will require a better mapping of threshold wind velocities, vegetation dynamics, and surface conditions (soil moisture and land use) especially in the sensitive regions identified here, as well as improved ability to address small-scale convective processes producing dust via cold pool (haboob) events frequent in monsoon regimes.

  19. MAMAP - a new spectrometer system for column-averaged methane and carbon dioxide observations from aircraft: retrieval algorithm and first inversions for point source emission rates

    NASA Astrophysics Data System (ADS)

    Krings, T.; Gerilowski, K.; Buchwitz, M.; Reuter, M.; Tretner, A.; Erzinger, J.; Heinze, D.; Pflüger, U.; Burrows, J. P.; Bovensmann, H.

    2011-09-01

    MAMAP is an airborne passive remote sensing instrument designed to measure the dry columns of methane (CH4) and carbon dioxide (CO2). The MAMAP instrument comprises two optical grating spectrometers: the first observing in the short wave infrared band (SWIR) at 1590-1690 nm to measure CO2 and CH4 absorptions, and the second in the near infrared (NIR) at 757-768 nm to measure O2 absorptions for reference/normalisation purposes. MAMAP can be operated in both nadir and zenith geometry during the flight. Mounted on an aeroplane, MAMAP surveys areas on regional to local scales with a ground pixel resolution of approximately 29 m × 33 m for a typical aircraft altitude of 1250 m and a velocity of 200 km h-1. The retrieval precision of the measured column relative to background is typically ≲ 1% (1σ). MAMAP measurements are valuable to close the gap between satellite data, having global coverage but with a rather coarse resolution, on the one hand, and highly accurate in situ measurements with sparse coverage on the other hand. In July 2007, test flights were performed over two coal-fired power plants operated by Vattenfall Europe Generation AG: Jänschwalde (27.4 Mt CO2 yr-1) and Schwarze Pumpe (11.9 Mt CO2 yr-1), about 100 km southeast of Berlin, Germany. By using two different inversion approaches, one based on an optimal estimation scheme to fit Gaussian plume models from multiple sources to the data, and another using a simple Gaussian integral method, the emission rates can be determined and compared with emissions reported by Vattenfall Europe. An extensive error analysis for the retrieval's dry column results (XCO2 and XCH4) and for the two inversion methods has been performed. Both methods - the Gaussian plume model fit and the Gaussian integral method - are capable of deriving estimates for strong point source emission rates that are within ±10% of the reported values, given appropriate flight patterns and detailed knowledge of wind conditions.

  20. Ultrafast spontaneous emission source using plasmonic nanoantennas

    PubMed Central

    Hoang, Thang B.; Akselrod, Gleb M.; Argyropoulos, Christos; Huang, Jiani; Smith, David R.; Mikkelsen, Maiken H.

    2015-01-01

    Typical emitters such as molecules, quantum dots and semiconductor quantum wells have slow spontaneous emission with lifetimes of 1–10 ns, creating a mismatch with high-speed nanoscale optoelectronic devices such as light-emitting diodes, single-photon sources and lasers. Here we experimentally demonstrate an ultrafast (<11 ps) yet efficient source of spontaneous emission, corresponding to an emission rate exceeding 90 GHz, using a hybrid structure of single plasmonic nanopatch antennas coupled to colloidal quantum dots. The antennas consist of silver nanocubes coupled to a gold film separated by a thin polymer spacer layer and colloidal core–shell quantum dots, a stable and technologically relevant emitter. We show an increase in the spontaneous emission rate of a factor of 880 and simultaneously a 2,300-fold enhancement in the total fluorescence intensity, which indicates a high radiative quantum efficiency of ∼50%. The nanopatch antenna geometry can be tuned from the visible to the near infrared, providing a promising approach for nanophotonics based on ultrafast spontaneous emission. PMID:26212857

  1. Ultrafast spontaneous emission source using plasmonic nanoantennas.

    PubMed

    Hoang, Thang B; Akselrod, Gleb M; Argyropoulos, Christos; Huang, Jiani; Smith, David R; Mikkelsen, Maiken H

    2015-07-27

    Typical emitters such as molecules, quantum dots and semiconductor quantum wells have slow spontaneous emission with lifetimes of 1-10 ns, creating a mismatch with high-speed nanoscale optoelectronic devices such as light-emitting diodes, single-photon sources and lasers. Here we experimentally demonstrate an ultrafast (<11 ps) yet efficient source of spontaneous emission, corresponding to an emission rate exceeding 90 GHz, using a hybrid structure of single plasmonic nanopatch antennas coupled to colloidal quantum dots. The antennas consist of silver nanocubes coupled to a gold film separated by a thin polymer spacer layer and colloidal core-shell quantum dots, a stable and technologically relevant emitter. We show an increase in the spontaneous emission rate of a factor of 880 and simultaneously a 2,300-fold enhancement in the total fluorescence intensity, which indicates a high radiative quantum efficiency of ∼50%. The nanopatch antenna geometry can be tuned from the visible to the near infrared, providing a promising approach for nanophotonics based on ultrafast spontaneous emission.

  2. Ultrafast spontaneous emission source using plasmonic nanoantennas

    NASA Astrophysics Data System (ADS)

    Hoang, Thang B.; Akselrod, Gleb M.; Argyropoulos, Christos; Huang, Jiani; Smith, David R.; Mikkelsen, Maiken H.

    2015-07-01

    Typical emitters such as molecules, quantum dots and semiconductor quantum wells have slow spontaneous emission with lifetimes of 1-10 ns, creating a mismatch with high-speed nanoscale optoelectronic devices such as light-emitting diodes, single-photon sources and lasers. Here we experimentally demonstrate an ultrafast (<11 ps) yet efficient source of spontaneous emission, corresponding to an emission rate exceeding 90 GHz, using a hybrid structure of single plasmonic nanopatch antennas coupled to colloidal quantum dots. The antennas consist of silver nanocubes coupled to a gold film separated by a thin polymer spacer layer and colloidal core-shell quantum dots, a stable and technologically relevant emitter. We show an increase in the spontaneous emission rate of a factor of 880 and simultaneously a 2,300-fold enhancement in the total fluorescence intensity, which indicates a high radiative quantum efficiency of ~50%. The nanopatch antenna geometry can be tuned from the visible to the near infrared, providing a promising approach for nanophotonics based on ultrafast spontaneous emission.

  3. Endocrine disrupting chemical emissions from combustion sources: diesel particulate emissions and domestic waste open burn emissions

    NASA Astrophysics Data System (ADS)

    Sidhu, Sukh; Gullett, Brian; Striebich, Richard; Klosterman, Joy; Contreras, Jesse; DeVito, Michael

    Emissions of endocrine disrupting chemicals (EDCs) from combustion sources are poorly characterized due to the large number of compounds present in the emissions, the complexity of the analytical separations required, and the uncertainty regarding identification of chemicals with endocrine effects. In this work, multidimensional gas chromatographic-mass spectrometry (MDGC-MS) was used to characterize emissions from both controlled (diesel engine) and uncontrolled (open burning of domestic waste) combustion sources. The results of this study suggest that, by using MDGC-MS, one can resolve a much greater percentage of the chromatogram and identify about 84% of these resolved compounds. This increase in resolution helped to identify and quantify various classes of polycyclic aromatic hydrocarbons (PAHs) in the combustion emissions that had not been identified previously. Significant emissions (when compared to industrial sources) of known EDCs, dioctyl phthalate (over ˜2,500,000 kg year -1) and bisphenol A (over ˜75,000 kg year -1) were estimated from uncontrolled domestic waste burning. Emissions of several suspected EDCs (oxygenated PAHs) were observed in both diesel soot and the uncontrolled domestic waste burn samples. The emission rates of known and suspected EDCs estimated in this study suggest that combustion emissions need to be characterized for EDCs to further assess its importance as a source of EDC exposure.

  4. VALIDATION OF A METHOD FOR ESTIMATING POLLUTION EMISSION RATES FROM AREA SOURCES USING OPEN-PATH FTIR SEPCTROSCOPY AND DISPERSION MODELING TECHNIQUES

    EPA Science Inventory

    The paper describes a methodology developed to estimate emissions factors for a variety of different area sources in a rapid, accurate, and cost effective manner. he methodology involves using an open-path Fourier transform infrared (FTIR) spectrometer to measure concentrations o...

  5. Other Production Emissions Sources- September 2012 Workshop

    EPA Pesticide Factsheets

    View a presentation on other production emissions sources, presented at the Stakeholder Workshop on Natural Gas in the Inventory of U.S. Greenhouse Gas (GHG) Emissions and Sinks on Thursday September, 13, 2012.

  6. Characterizing sources of emissions from wildland fires

    Treesearch

    Roger D. Ottmar; Ana Isabel Miranda; David V. Sandberg

    2009-01-01

    Smoke emissions from wildland fire can be harmful to human health and welfare, impair visibility, and contribute to greenhouse gas emissions. The generation of emissions and heat release need to be characterized to estimate the potential impacts of wildland fire smoke. This requires explicit knowledge of the source, including size of the area burned, burn period,...

  7. Attributing Atmospheric Methane to Anthropogenic Emission Sources.

    PubMed

    Allen, David

    2016-07-19

    Methane is a greenhouse gas, and increases in atmospheric methane concentration over the past 250 years have driven increased radiative forcing of the atmosphere. Increases in atmospheric methane concentration since 1750 account for approximately 17% of increases in radiative forcing of the atmosphere, and that percentage increases by approximately a factor of 2 if the effects of the greenhouse gases produced by the atmospheric reactions of methane are included in the assessment. Because of the role of methane emissions in radiative forcing of the atmosphere, the identification and quantification of sources of methane emissions is receiving increased scientific attention. Methane emission sources include biogenic, geogenic, and anthropogenic sources; the largest anthropogenic sources are natural gas and petroleum systems, enteric fermentation (livestock), landfills, coal mining, and manure management. While these source categories are well-known, there is significant uncertainty in the relative magnitudes of methane emissions from the various source categories. Further, the overall magnitude of methane emissions from all anthropogenic sources is actively debated, with estimates based on source sampling extrapolated to regional or national scale ("bottom-up analyses") differing from estimates that infer emissions based on ambient data ("top-down analyses") by 50% or more. To address the important problem of attribution of methane to specific sources, a variety of new analytical methods are being employed, including high time resolution and highly sensitive measurements of methane, methane isotopes, and other chemical species frequently associated with methane emissions, such as ethane. This Account describes the use of some of these emerging measurements, in both top-down and bottom-up methane emission studies. In addition, this Account describes how data from these new analytical methods can be used in conjunction with chemical mass balance (CMB) methods for source

  8. Atmospheric process evaluation of mobile source emissions

    SciTech Connect

    1995-07-01

    During the past two decades there has been a considerable effort in the US to develop and introduce an alternative to the use of gasoline and conventional diesel fuel for transportation. The primary motives for this effort have been twofold: energy security and improvement in air quality, most notably ozone, or smog. The anticipated improvement in air quality is associated with a decrease in the atmospheric reactivity, and sometimes a decrease in the mass emission rate, of the organic gas and NO{sub x} emissions from alternative fuels when compared to conventional transportation fuels. Quantification of these air quality impacts is a prerequisite to decisions on adopting alternative fuels. The purpose of this report is to present a critical review of the procedures and data base used to assess the impact on ambient air quality of mobile source emissions from alternative and conventional transportation fuels and to make recommendations as to how this process can be improved. Alternative transportation fuels are defined as methanol, ethanol, CNG, LPG, and reformulated gasoline. Most of the discussion centers on light-duty AFVs operating on these fuels. Other advanced transportation technologies and fuels such as hydrogen, electric vehicles, and fuel cells, will not be discussed. However, the issues raised herein can also be applied to these technologies and other classes of vehicles, such as heavy-duty diesels (HDDs). An evaluation of the overall impact of AFVs on society requires consideration of a number of complex issues. It involves the development of new vehicle technology associated with engines, fuel systems, and emission control technology; the implementation of the necessary fuel infrastructure; and an appropriate understanding of the economic, health, safety, and environmental impacts associated with the use of these fuels. This report addresses the steps necessary to properly evaluate the impact of AFVs on ozone air quality.

  9. Radiation source with shaped emission

    DOEpatents

    Kubiak, Glenn D.; Sweatt, William C.

    2003-05-13

    Employing a source of radiation, such as an electric discharge source, that is equipped with a capillary region configured into some predetermined shape, such as an arc or slit, can significantly improve the amount of flux delivered to the lithographic wafers while maintaining high efficiency. The source is particularly suited for photolithography systems that employs a ringfield camera. The invention permits the condenser which delivers critical illumination to the reticle to be simplified from five or more reflective elements to a total of three or four reflective elements thereby increasing condenser efficiency. It maximizes the flux delivered and maintains a high coupling efficiency. This architecture couples EUV radiation from the discharge source into a ring field lithography camera.

  10. Jovian S emission: Model of radiation source

    NASA Astrophysics Data System (ADS)

    Ryabov, B. P.

    1994-04-01

    A physical model of the radiation source and an excitation mechanism have been suggested for the S component in Jupiter's sporadic radio emission. The model provides a unique explanation for most of the interrelated phenomena observed, allowing a consistent interpretation of the emission cone structure, behavior of the integrated radio spectrum, occurrence probability of S bursts, location and size of the radiation source, and fine structure of the dynamic spectra. The mechanism responsible for the S bursts is also discussed in connection with the L type emission. Relations are traced between parameters of the radio emission and geometry of the Io flux tube. Fluctuations in the current amplitude through the tube are estimated, along with the refractive index value and mass density of the plasma near the radiation source.

  11. Evaluation of Mobile Source Emissions and Trends

    NASA Astrophysics Data System (ADS)

    Dallmann, Timothy Ryan

    Mobile sources contribute significantly to air pollution problems. Relevant pollutants include numerous gaseous and particle-phase species that can affect human health, ecosystems, and climate. Accurate inventories of emissions from these sources are needed to help understand possible adverse impacts, and to develop effective air quality management strategies. Unfortunately large uncertainties persist in the understanding of mobile source emissions, and how these emissions are changing over time. This dissertation aims to evaluate long-term trends in mobile source emissions in the United States, and to make detailed measurements of emissions from present-day fleets of on-road vehicles operating in California. Long-term trends in mobile source emissions of nitrogen oxides (NO x) and fine particulate matter (PM2.5) in the United States were investigated through development of a fuel-based emission inventory. Annual emissions from on- and off-road gasoline and diesel engines were quantified for the years 1996-2006. Diesel engines were found to be the dominant mobile source of NOx and PM2.5, and on-road diesel vehicles were identified as the single largest anthropogenic source of NOx emissions in the United States as of 2005. The importance of diesel engines as a source of exhaust particulate matter emissions has led to the recent introduction of advanced emission control technologies in the United States, such as diesel particle filters (DPF), which have been required since 2007 for all new on-road heavy-duty (HD) diesel engines. In addition to national requirements for the use of such control devices on new engines, California has mandated accelerated clean-up of statewide emissions from older in-use diesel engines. The plume capture method was further applied to measure emissions from a more diverse population of trucks observed at the Caldecott tunnel in summer 2010. Emissions from hundreds of individual trucks were measured, and emission factor distributions were

  12. Controlling NOx emission from industrial sources

    SciTech Connect

    Srivastava, R.K.; Nueffer, W.; Grano, D.; Khan, S.; Staudt, J.E.; Jozewicz, W.

    2005-07-01

    A number of regulatory actions focused on reducing NOx emissions from stationary combustion sources have been taken in the United States in the last decade. These actions include the Acid Rain NOx regulations, the Ozone Transport Commission's NOx Budget Program, and the NOx SIP Call rulemakings. In addition to these regulations, the recent Interstate Air Quality Rulemaking proposal and other bills in the Congress are focusing on additional reductions of NOx. Industrial combustion sources accounted for about 18016 of NOx emissions in the United States in 2000 and constituted the second largest emitting source category within stationary sources, only behind electric utility sources. Based on these data, reduction of NOx emissions from industrial combustion sources is an important consideration in efforts undertaken to address the environmental concerns associated with NOx. This paper discusses primary and secondary NOx control technologies applicable to various major categories of industrial sources. The sources considered in this paper include large boilers, furnaces and fired heaters, combustion turbines, large IC engines, and cement kilns. For each source category considered in this paper, primary NOx controls are discussed first, followed by a discussion of secondary NOx controls.

  13. ENDOCRINE DISRUPTING CHEMICAL EMISSIONS FROM COMBUSTION SOURCES: DIESEL PARTICULATE EMISSIONS AND DOMESTIC WASTE OPEN BURN EMISSIONS

    EPA Science Inventory

    Emissions of endocrine disrupting chemicals (EDCs) from combustion sources are poorly characterized due to the large number of compounds present in the emissions, the complexity of the analytical separations required, and the uncertainty regarding identification of chemicals with...

  14. Coherent emission of light by thermal sources

    NASA Astrophysics Data System (ADS)

    Greffet, Jean-Jacques; Carminati, Rémi; Joulain, Karl; Mulet, Jean-Philippe; Mainguy, Stéphane; Chen, Yong

    2002-03-01

    A thermal light-emitting source, such as a black body or the incandescent filament of a light bulb, is often presented as a typical example of an incoherent source and is in marked contrast to a laser. Whereas a laser is highly monochromatic and very directional, a thermal source has a broad spectrum and is usually quasi-isotropic. However, as is the case with many systems, different behaviour can be expected on a microscopic scale. It has been shown recently that the field emitted by a thermal source made of a polar material is enhanced by more than four orders of magnitude and is partially coherent at a distance of the order of 10 to 100nm. Here we demonstrate that by introducing a periodic microstructure into such a polar material (SiC) a thermal infrared source can be fabricated that is coherent over large distances (many wavelengths) and radiates in well defined directions. Narrow angular emission lobes similar to antenna lobes are observed and the emission spectra of the source depends on the observation angle-the so-called Wolf effect. The origin of the coherent emission lies in the diffraction of surface-phonon polaritons by the grating.

  15. 40 CFR 74.23 - 1985 Allowable SO2 emissions rate.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... (CONTINUED) SULFUR DIOXIDE OPT-INS Allowance Calculations for Combustion Sources § 74.23 1985 Allowable SO2 emissions rate. (a) Data requirements. (1) The designated representative of the combustion source shall... data: (i) Allowable SO2 emissions rate of the combustion source expressed in lbs/mmBtu as defined...

  16. Calendar Year 2016 Stationary Source Emissions Inventory

    SciTech Connect

    Evelo, Stacie

    2017-01-01

    The City of Albuquerque (COA) Environmental Health Department Air Quality Program has issued stationary source permits and registrations the Department of Energy/Sandia Field Office for operations at the Sandia National Laboratories/New Mexico. This emission inventory report meets the annual reporting compliance requirements for calendar year (CY) 2016 as required by the COA.

  17. CONTROLLING NOX EMISSION FROM INDUSTRIAL SOURCES

    EPA Science Inventory

    A number of regulatory actions focused on reducing NOx emissions from stationary combustion sources have been taken in the United States in the last decade. These actions include the Acid Rain NOx regulations, the Ozone Transport Commission's NOx ...

  18. Synchro-Compton emission from superluminal sources

    NASA Technical Reports Server (NTRS)

    Marscher, Alan P.

    1987-01-01

    The application of synchro-Compton theory to real compact radio sources, the question of a self-Compton origin of the X-rays in radio-loud quasars and active galactic nuclei, and the phenomenology of superluminal motion are discussed in a review of research concerning synchro-Compton emission from superluminal sources. After examining the basic synchro-Compton theory of ideal sources, applications of the theory to real sources is discussed. It is concluded that the Compton problem and total energy requirements are not substantially mitigated by considering source structures more complicated than the multiple, uniform-component model used by most investigators. Also, alternatives to the standard model of superluminal motion are discussed, focusing on the assumptions usually made when interpreting superluminal sources.

  19. Synchro-Compton emission from superluminal sources

    NASA Technical Reports Server (NTRS)

    Marscher, Alan P.

    1987-01-01

    The application of synchro-Compton theory to real compact radio sources, the question of a self-Compton origin of the X-rays in radio-loud quasars and active galactic nuclei, and the phenomenology of superluminal motion are discussed in a review of research concerning synchro-Compton emission from superluminal sources. After examining the basic synchro-Compton theory of ideal sources, applications of the theory to real sources is discussed. It is concluded that the Compton problem and total energy requirements are not substantially mitigated by considering source structures more complicated than the multiple, uniform-component model used by most investigators. Also, alternatives to the standard model of superluminal motion are discussed, focusing on the assumptions usually made when interpreting superluminal sources.

  20. Polychlorinated Biphenyl Sources, Emissions, and Environmental Levels in school Buildings (PCB Workshop presentation)

    EPA Science Inventory

    Measure PCB emission rates from primary sources in laboratory chambersMeasure transport and sorption by materials and dust in laboratory chambersCharacterize PCBs in school building materialsEstimate PCB emission rates from sources in schoolsExamine congener patterns in sources a...

  1. Polychlorinated Biphenyl Sources, Emissions, and Environmental Levels in school Buildings (PCB Workshop presentation)

    EPA Science Inventory

    Measure PCB emission rates from primary sources in laboratory chambersMeasure transport and sorption by materials and dust in laboratory chambersCharacterize PCBs in school building materialsEstimate PCB emission rates from sources in schoolsExamine congener patterns in sources a...

  2. Source emission-pattern polynomial representation

    NASA Astrophysics Data System (ADS)

    Flores-Hernandez, Ricardo; De Villa, Francisco

    1990-12-01

    A method to obtain accurate thickness data to characterize the emission patterns of evaporation sources is described. Thickness data is obtained through digital image processing algorithms applied to the monochromatic transmission bands digitized from a set of multilayer Fabry-Perot filters deposited on large flat circular substrates. These computer image-processed taper-thickness patterns are reduced to orthonormal polynomial series expansions in two steps, using Tschebyshev and associated Legendre polynomials. The circular glass substrates employed to characterize each type of evaporation source are kept stationary during the evaporation process of evaporation of each layer to obtain the specific thickness distribution for each type of source.

  3. Methane emissions from grazing cattle using point-source dispersion.

    PubMed

    McGinn, S M; Turner, D; Tomkins, N; Charmley, E; Bishop-Hurley, G; Chen, D

    2011-01-01

    The ability to accurately measure greenhouse gas (GHG) emissions is essential to gauge our ability to reduce these emissions. Enteric methane from ruminants is an important but often difficult source to quantify since it depends on the amount and type of feed intake. Unfortunately, many of the available measurement techniques for estimating enteric methane emissions can impose a change in feed intake. Our study evaluates a nonintrusive technique that uses a novel approach (point-source dispersion with multiple open-path concentrations) to calculate enteric methane emissions from grazing cattle, reported as the major source of GHG in many countries, particularly Australia. A scanner with a mounted open-path laser was used to measure methane concentration across five paths above a paddock containing 18 grazing cattle over 16 d. These data were used along with wind statistics in a dispersion model (WindTrax) to estimate an average herd methane emission rate over 10-mm intervals. Enteric methane emissions from the herd grazing a combination of Rhodes grass (Chlotis gayana Kunth) and Leucaena [Leucaena leucocephala (Lam.)] averaged (+/- SD) 141 (+/- 147) g animal(-1) d(-1). In a release-recovery experiment, the technique accounted for 77% of the released methane at a single point. Our study shows the technique generates more reliable methane emissions during daytime (unstable stratification).

  4. Modeling study of natural emissions, source apportionment, and emission control of atmospheric mercury

    NASA Astrophysics Data System (ADS)

    Shetty, Suraj K.

    ) and CAMNet (Canadian Atmospheric Mercury Measurement Network). The model estimated a total deposition of 474 Mg yr-1 to the CONUS (Contiguous United States) domain, with two-thirds being dry deposited. Reactive gaseous mercury contributed the most to 60% of deposition. Emission speciation distribution is a key factor for local deposition as contribution from large point sources can be as high as 75% near (< 100 km) the emission sources, indicating that emission reduction may result in direct deposition decrease near the source locations. Among the sources, BC contributes to about 68% to 91% of total deposition. Excluding the BC's contribution, EGU contributes to nearly 50% of deposition caused by CONUS emissions in the Northeast, Southeast and East Central regions, while emissions from natural processes are more important in the Pacific and West Central regions (contributing up to 40% of deposition). The modeling results implies that implementation of the new emission standards proposed by USEPA (United States Environmental Protection Agency) would significantly benefit regions that have larger contributions from EGU sources. Control of mercury emissions from coal combustion processes has attracted great attention due to its toxicity and the emission-control regulations and has lead to advancement in state-of-the-art control technologies that alleviate the impact of mercury on ecosystem and human health. This part of the work applies a sorption model to simulate adsorption of mercury in flue gases, onto a confined-bed of activated carbon. The model's performances were studied at various flue gas flow rates, inlet mercury concentrations and adsorption bed temperatures. The process simulated a flue gas, with inlet mercury concentration of 300 ppb, entering at a velocity of 0.3 m s-1 from the bottom into a fixed bed (inside bed diameter of 1 m and 3 m bed height; bed temperature of 25 °C) of activated carbon (particle size of 0.004 m with density of 0.5 g cm-3 and

  5. Radio frequency glow discharge source with integrated voltage and current probes used for sputtering rate and emission yield measurements at insulating samples.

    PubMed

    Wilken, L; Hoffmann, V; Wetzig, K

    2005-10-01

    Radio frequency glow discharge optical emission spectroscopy (RF-GD-OES) is routinely used for the chemical analysis of solid samples. Two independent electrical signals from the discharge are required for quantification. When sputtering insulating samples, the voltage over the discharge is not directly measurable. The coupling capacity of the sample is required in order to calculate the discharge voltage. A procedure is outlined where the coupling capacity is determined using an electrical measurement without discharge. The calculated time-dependent discharge voltage and current are evaluated using a plasma equivalent circuit. An insulating sample is sputtered at constant cathode voltage and current. The emission yield for an aluminium line is comparable to that of conducting reference material.

  6. Mobile Source Emissions Regulatory Compliance Data

    EPA Pesticide Factsheets

    The Engine and Vehicle Compliance Certification and Fuel Economy Inventory contains measured emissions and fuel economy compliance information for all types of vehicles (mobile sources of air pollution) excluding snowmobile, marine (diesel), and heavy duty engines whichsummary data is updated on an annual basis. Data is collected by EPA to certify compliance with the applicable fuel economy provisions of the Clean Air Act, Energy Policy and Conservation Act (EPCA) and the Energy Independent Security Act (EISA) of 2007.

  7. eGRID 2014 subregion GHG output emission rates

    EPA Pesticide Factsheets

    This page contains the eGRID 2014 subregion GHG output emission rates. Annual total output emission rates for greenhouse gases (GHGs) can be used as default factors for estimating GHG emissions from electricity use when developing a carbon footprint

  8. Krakow conference on low emissions sources: Proceedings

    SciTech Connect

    Pierce, B.L.; Butcher, T.A.

    1995-12-31

    The Krakow Conference on Low Emission Sources presented the information produced and analytical tools developed in the first phase of the Krakow Clean Fossil Fuels and Energy Efficiency Program. This phase included: field testing to provide quantitative data on missions and efficiencies as well as on opportunities for building energy conservation; engineering analysis to determine the costs of implementing pollution control; and incentives analysis to identify actions required to create a market for equipment, fuels, and services needed to reduce pollution. Collectively, these Proceedings contain reports that summarize the above phase one information, present the status of energy system management in Krakow, provide information on financing pollution control projects in Krakow and elsewhere, and highlight the capabilities and technologies of Polish and American companies that are working to reduce pollution from low emission sources. It is intended that the US reader will find in these Proceedings useful results and plans for control of pollution from low emission sources that are representative of heating systems in central and Eastern Europe. Selected papers are indexed separately for inclusion in the Energy Science and Technology Database.

  9. NMHC emissions from Asia: sources and transport

    NASA Astrophysics Data System (ADS)

    Shirai, T.; Blake, D. R.; Barletta, B.; Meinardi, S.; Rowland, F. S.; Chan, J. C.; Takegawa, N.; Kondo, Y.; Koike, M.; Kita, K.; Takigawa, M.; Kawakami, S.; Ogawa, T.

    2002-12-01

    Recent rapid industrialization and economic growth in Asia changed the industrial structure, land use, and people's lifestyle resulting in a dramatic change in the amount and composition of the gas emissions from Asia. Because emissions can be transported very rapidly once convected to the free troposphere, Asian emissions can affect both local and regional air quality and climate. To access the impact of changing emission from Asia, an airborne observation campaign PEACE (the Pacific Exploration of Asian Continental Emission) phase-A and B were conducted in January and April - May 2002, respectively, sponsored by NASDA (National Space Development Agency of Japan). The concentrations of NMHCs (nonmethanehydrocarbons) and halocarbons were obtained by whole air sampling and subsequent gas chromatography analyses in the laboratory. Quantified onboard the aircraft were CO, CO2, O3, NO, NO2, NOy, H2O, SO2, aerosols, and condensation nuclei. The experiment was conducted in the vicinity of Japan and PEACE-A and B represent the local winter and spring weather conditions. The trace gas distributions in the lower troposphere were often influenced by local pollution (i.e. from Japan, Korea) while those of the long-range transport (i.e. from Europe) were occasionally seen in the upper troposphere. This is confirmed by the airmass age estimation using the ratios of short-lived gases (i.e. C2H4) vs. more stable compounds (i.e. CO). Emissions from China were distinguished using data obtained from ground-based sampling and measurements. Transport from China was seen both in the lower troposphere and upper troposphere. Some case studies on source identification will be discussed.

  10. Framework for Assessing Biogenic CO2 Emissions from Stationary Sources

    EPA Science Inventory

    This revision of the 2011 report, Accounting Framework for Biogenic CO2 Emissions from Stationary Sources, evaluates biogenic CO2 emissions from stationary sources, including a detailed study of the scientific and technical issues associated with assessing biogenic carbon dioxide...

  11. Framework for Assessing Biogenic CO2 Emissions from Stationary Sources

    EPA Science Inventory

    This revision of the 2011 report, Accounting Framework for Biogenic CO2 Emissions from Stationary Sources, evaluates biogenic CO2 emissions from stationary sources, including a detailed study of the scientific and technical issues associated with assessing biogenic carbon dioxide...

  12. Measuring Greenhouse-Gas Emissions from a Synthetic Tracer Source

    NASA Astrophysics Data System (ADS)

    Wang, W.; Liu, W.; Zhang, T.; Lu, Y.

    2014-05-01

    This paper describes a controlled tracer-release experiment in which methane was released from a synthetic source at known rates. An open-path Fourier transform infrared (OP-FTIR) spectroscopy system was used to measure line-averaged methane concentrations downwind of the source. A Lagrangian stochastic (LS) dispersion model was employed to infer emission rates from downwind gas concentrations. The main purpose of our study was to investigate the ability of our open-path FTIR system combined with the LS dispersion model to accurately measure greenhouse gas emissions. In our study, the average ratio of the estimated emissions to actual release rates QLS/Q for CH4 was about 0.86 (σQLS/Q = 0.2, n = 6) and 0.84 (σQLS/Q = 0.22, n = 3) after data fi ltering for a 15- and a 30- min period, respectively. Although there is a limited amount of data in this experiment, the results demonstrate the potential of the measurement system for accurate quantifi cation of greenhouse gas emissions.

  13. Denitrification as a Source of NO Emissions using Isotope Techniques

    NASA Astrophysics Data System (ADS)

    Cardenas, Laura; Loick, Nadine; Abalos, Diego; Dixon, Liz; Vallejo, Antonio; Watson, Catherine; McGeough, Karen; Well, Reinhard; Matthews, Peter

    2015-04-01

    Agricultural soils are a major source of nitric- (NO) and nitrous oxide (N2O) which are produced and consumed by biotic and abiotic soil processes. The dominant sources of NO and N2O are microbial nitrification and denitrification. Depending on the environmental conditions such as substrate availability, pH and water filled pore space (WFPS) N2O emissions have been attributed to both processes, whereas NO emissions are thought to predominantly derive from nitrification. This is due to the fact that the environmental factors which promote denitrifying conditions also restrict gaseous diffusivity causing consumption of the highly reactive NO. Recent findings however challenge this assumption indicating that denitrification can be a significant source of NO. Attributing gaseous emissions to specific soil processes is still difficult; however, advanced isotopic methods show great potential. Labelling methods rely on the use of 15N enriched substrates, whereas isotopomer analyses rely on differences in the utilisation of heavy vs light N and O isotopes at natural abundance. The present study analysed the effect of different enrichment levels on gaseous emissions using the gas-flow-soil-core technique (Cardenas et al 2003). This system provides continuous measurements of NO, N2O as well as N2 fluxes by exchanging the normal atmosphere with a mixture of He:O2 (80:20). This was combined with 15N labelled isotopic techniques and isotopomer measurements to determine the source and processes responsible for the measured N-emissions. Nutrient solutions were applied containing KNO3 with 15N at natural abundance, 5 atom% and 20 atom% enrichment at a rate of 75 kg N ha-1 together with glucose at a rate of 400 kg C ha-1. Results showed that at the higher level of enrichment gaseous emissions were affected by showing an increase in emissions of NO and N2O. Additionally, under denitrifying conditions (high WFPS and NO3- availability) denitrification played a key role in NO emissions

  14. VOC emission rates and emission factors for a sheetfed offset printing shop.

    PubMed

    Wadden, R A; Scheff, P A; Franke, J E; Conroy, L M; Javor, M; Keil, C B; Milz, S A

    1995-04-01

    Emission rates were determined during production for a sheetfed offset printing shop by combining the measured concentrations and ventilation rates with mass balance models that characterized the printing space. Air samples were collected simultaneously on charcoal tubes for 12 separate 1-hour periods at 6 locations. Air samples and cleaning solvents were analyzed by gas chromatography for total volatile organic compounds (VOC) and 13 hydrocarbons. The average VOC emission rate was 470 g/hr with a range of 160-1100 g/hr. These values were in good agreement with the amounts of VOC, hexane, toluene, and aromatic C9s determined from estimated solvent usage and measured solvent compositions. Comparison of the emission rates with source activities indicated an emission factor of 30-51 g VOC/press cleaning. Based on the test observations it was estimated that this typical small printing facility was likely to release 1-2 T VOC/year. The methodology also may be useful for the surface coating industry, as emission rates in this study were determined without recourse to a temporary total enclosure and without interfering with worker activities, increasing worker exposure, or increasing safety and explosion hazards.

  15. Source gases: Concentrations, emissions, and trends

    NASA Technical Reports Server (NTRS)

    Fraser, Paul J.; Harriss, Robert; Penkett, Stuart A.; Makide, Yoshihiro; Sanhueza, Eugenio; Alyea, Fred N.; Rowland, F. Sherwood; Blake, Don; Sasaki, Toru; Cunnold, Derek M.

    1991-01-01

    Source gases are defined as those gases that influence levels of stratospheric ozone (O3) by transporting species containing halogen, hydrogen, and nitrogen to the stratosphere. Examples are the CFC's, methane (CH4), and nitrous oxide (N2O). Other source gases that also come under consideration in an atmospheric O3 context are those that are involved in the O3 or hydroxyl (OH) radical chemistry of the troposphere. Examples are CH4, carbon monoxide (CO), and nonmethane hydrocarbons (NMHC's). Most of the source gases, along with carbon dioxide (CO2) and water vapor (H2O), are climatically significant and thus affect stratospheric O3 levels by their influence on stratospheric temperatures. Carbonyl sulphide (COS) could affect stratospheric O3 through maintenance of the stratospheric sulphate aerosol layer, which may be involved in heterogeneous chlorine-catalyzed O3 destruction. The previous reviews of trends and emissions of source gases, either from the context of their influence on atmospheric O3 or global climate change, are updated. The current global abundances and concentration trends of the trace gases are given in tabular format.

  16. Source characteristics of Jovian hectometric radio emissions

    NASA Technical Reports Server (NTRS)

    Reiner, M. J.; Fainberg, J.; Stone, R. G.

    1993-01-01

    Direct confirmation that low-frequency Jovian hectometric (HOM) radio emissions centered near 0 deg central meridian longitude consist of distinct, oppositely polarized northern and southern beams has been achieved using data from the Unified Radio and Plasma Wave (URAP) experiment on the Ulysses spacecraft during the Ulysses-Jupiter encounter in early February 1992. Distinct northern and southern beams were observed in the frequency range from approximately 300 kHz to 1 MHz for at least eight Jovian rotations during the Ulysses inbound pass at distances from 100 to 40 R(sub j). The radiation from the two magnetic hemispheres was measured from different Jovigraphic longitudes and magnetic (or centrifugal) latitudes. Observed temporal variations in the radio intensities, with time scales on the order of 30 min, may result either from longitudinal variations of the HOM sources or from longitudinal density variations in the Io plasma torus. Using the URAP direction-finding capabilities and assuming a tilted dipole planetary magnetic field model, the three-dimensional HOM source locations, the L shell through these source locations, and the beam opening angles were independently deduced. The HOM sources were found to originate at approximately 3 R(sub j) and on low L shells (L approximately 4 to 6), with beam opening angles ranging from 10 to 50 deg.

  17. Atmospheric polycyclic aromatic hydrocarbons: Source attribution, emission factors and regulation

    NASA Astrophysics Data System (ADS)

    Ravindra, Khaiwal; Sokhi, Ranjeet; Van Grieken, René

    There is an increasing concern about the occurrence of polycyclic aromatic hydrocarbons (PAHs) in the environment as they are ubiquitous in ambient air and some of them are among the strongest known carcinogens. PAHs and their derivatives are produced by the incomplete combustion of organic material arising, partly, from natural combustion such as forest and volcanic eruption, but with the majority due to anthropogenic emissions. The PAH concentration varies significantly in various rural and urban environments and is mainly influenced by vehicular and domestic emissions. The review serves as a database to identify and characterize the emission sources of PAHs and hence various approaches including diagnostic ratio (DR) and principal component analysis (PCA) are discussed in detail. These approaches allow individual PAHs to be associated with their origin sources. The factors that effect PAH emission and estimated emission rate are also discussed in this paper. Although the levels of low molecular weight PAHs are high in vapor phase, most of the probable human carcinogenic PAHs are found to be associated with particulate matter, especially in fine mode particles in ambient air. Many countries have proposed a non-mandatory concentration limit for PAHs, whereas the health risk studies conducted in relation to PAH exposure, urge that these pollutants should be given a high priority when considering air quality management and reduction of impacts.

  18. Mobile Source Emissions Regulatory Compliance Data Inventory

    EPA Pesticide Factsheets

    The Mobile Source Emissions Regulatory Compliance Data Inventory data asset contains measured summary compliance information on light-duty, heavy-duty, and non-road engine manufacturers by model, as well as fee payment data required by Title II of the 1990 Amendments to the Clean Air Act, to certify engines for sale in the U.S. and collect compliance certification fees. Data submitted by manufacturers falls into 12 industries: Heavy Duty Compression Ignition, Marine Spark Ignition, Heavy Duty Spark Ignition, Marine Compression Ignition, Snowmobile, Motorcycle & ATV, Non-Road Compression Ignition, Non-Road Small Spark Ignition, Light-Duty, Evaporative Components, Non-Road Large Spark Ignition, and Locomotive. Title II also requires the collection of fees from manufacturers submitting for compliance certification. Manufacturers submit data on an annual basis, to document engine model changes for certification. Manufacturers also submit compliance information on already certified in-use vehicles randomly selected by the EPA (1) year into their life and (4) years into their life to ensure that emissions systems continue to function appropriately over time.The EPA performs targeted confirmatory tests on approximately 15% of vehicles submitted for certification. Confirmatory data on engines is associated with its corresponding submission data to verify the accuracy of manufacturer submission beyond standard business rules.Section 209 of the 1990 Amendments to the Clea

  19. High rates of methane emissions from south taiga wetland ponds.

    NASA Astrophysics Data System (ADS)

    Glagolev, M.; Kleptsova, I.; Maksyutov, S.

    2012-04-01

    Since wetland ponds are often assumed to be insignificant sources of methane, there is a limited data about its fluxes. In this study, we found surprisingly high rates of methane emission at several shallow ponds in the south taiga zone of West Siberia. Wetland ponds within the Great Vasyugan Mire ridge-hollow-pool patterned bog system were investigated. 22 and 24 flux measurements from ponds and surrounded mires, respectively, were simultaneously made by a static chamber method in July, 2011. In contrast to previous measurements, fluxes were measured using the small boat with floated chamber to avoid disturbance to the water volume. Since the ebullition is most important emission pathway, minimization of physical disturbance provoking gas bubbling significantly increases the data accuracy. Air temperature varied from 15 to 22° C during the measurements, and pH at different pond depths - from 4.4 to 5. As it was found, background emission from surrounding ridges and hollows was 1.7/2.6/3.3 mgC·m-2·h1 (1st/2nd/3rd quartiles). These rates are in a perfect correspondence with the typical methane emission fluxes from other south taiga bogs. Methane emission from wetland ponds turned out to be by order of magnitude higher (9.3/11.3/15.6 mgC·m-2·h1). Comparing to other measurements in West Siberia, many times higher emissions (70.9/111.6/152.3 mgC·m-2·h1) were found in forest-steppe and subtaiga fen ponds. On the contrary, West Siberian tundra lakes emit methane insignificantly, with the flux rate close to surrounding wetlands (about 0.2-0.3 mgC·m-2·h1). Apparently, there is a naturally determined distribution of ponds with different flux rates over different West Siberia climate-vegetation zones. Further investigations aiming at revelation of the zones with different fluxes would be helpful for total flux revision purposes. With respect to other studies, high emission rates were already detected, for instance, in Baltic ponds (Dzyuban, 2002) and U.K. lakes

  20. 40 CFR 74.24 - Current allowable SO2 emissions rate.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 16 2010-07-01 2010-07-01 false Current allowable SO2 emissions rate... PROGRAMS (CONTINUED) SULFUR DIOXIDE OPT-INS Allowance Calculations for Combustion Sources § 74.24 Current allowable SO2 emissions rate. The designated representative shall submit the following data: (a) Current...

  1. 40 CFR 74.24 - Current allowable SO2 emissions rate.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 16 2011-07-01 2011-07-01 false Current allowable SO2 emissions rate... PROGRAMS (CONTINUED) SULFUR DIOXIDE OPT-INS Allowance Calculations for Combustion Sources § 74.24 Current allowable SO2 emissions rate. The designated representative shall submit the following data: (a) Current...

  2. 40 CFR 74.24 - Current allowable SO 2 emissions rate.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 17 2014-07-01 2014-07-01 false Current allowable SO 2 emissions rate... PROGRAMS (CONTINUED) SULFUR DIOXIDE OPT-INS Allowance Calculations for Combustion Sources § 74.24 Current allowable SO 2 emissions rate. The designated representative shall submit the following data: (a) Current...

  3. 40 CFR 74.24 - Current allowable SO 2 emissions rate.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 17 2013-07-01 2013-07-01 false Current allowable SO 2 emissions rate... PROGRAMS (CONTINUED) SULFUR DIOXIDE OPT-INS Allowance Calculations for Combustion Sources § 74.24 Current allowable SO 2 emissions rate. The designated representative shall submit the following data: (a) Current...

  4. 40 CFR 74.24 - Current allowable SO2 emissions rate.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 17 2012-07-01 2012-07-01 false Current allowable SO2 emissions rate... PROGRAMS (CONTINUED) SULFUR DIOXIDE OPT-INS Allowance Calculations for Combustion Sources § 74.24 Current allowable SO2 emissions rate. The designated representative shall submit the following data: (a) Current...

  5. Constraining Emission Models of Luminous Blazar Sources

    SciTech Connect

    Sikora, Marek; Stawarz, Lukasz; Moderski, Rafal; Nalewajko, Krzysztof; Madejski, Greg; /KIPAC, Menlo Park /SLAC

    2009-10-30

    Many luminous blazars which are associated with quasar-type active galactic nuclei display broad-band spectra characterized by a large luminosity ratio of their high-energy ({gamma}-ray) and low-energy (synchrotron) spectral components. This large ratio, reaching values up to 100, challenges the standard synchrotron self-Compton models by means of substantial departures from the minimum power condition. Luminous blazars have also typically very hard X-ray spectra, and those in turn seem to challenge hadronic scenarios for the high energy blazar emission. As shown in this paper, no such problems are faced by the models which involve Comptonization of radiation provided by a broad-line-region, or dusty molecular torus. The lack or weakness of bulk Compton and Klein-Nishina features indicated by the presently available data favors production of {gamma}-rays via up-scattering of infrared photons from hot dust. This implies that the blazar emission zone is located at parsec-scale distances from the nucleus, and as such is possibly associated with the extended, quasi-stationary reconfinement shocks formed in relativistic outflows. This scenario predicts characteristic timescales for flux changes in luminous blazars to be days/weeks, consistent with the variability patterns observed in such systems at infrared, optical and {gamma}-ray frequencies. We also propose that the parsec-scale blazar activity can be occasionally accompanied by dissipative events taking place at sub-parsec distances and powered by internal shocks and/or reconnection of magnetic fields. These could account for the multiwavelength intra-day flares occasionally observed in powerful blazars sources.

  6. Emissivity Tuned Emitter for RTPV Power Sources

    SciTech Connect

    Carl M. Stoots; Robert C. O'Brien; Troy M. Howe

    2012-03-01

    Every mission launched by NASA to the outer planets has produced unexpected results. The Voyager I and II, Galileo, and Cassini missions produced images and collected scientific data that totally revolutionized our understanding of the solar system and the formation of the planetary systems. These missions were enabled by the use of nuclear power. Because of the distances from the Sun, electrical power was produced using the radioactive decay of a plutonium isotope. Radioisotopic Thermoelectric Generators (RTGs) used in the past and currently used Multi-Mission RTGs (MMRTGs) provide power for space missions. Unfortunately, RTGs rely on thermocouples to convert heat to electricity and are inherently inefficient ({approx} 3-7% thermal to electric efficiency). A Radioisotope Thermal Photovoltaic (RTPV) power source has the potential to reduce the specific mass of the onboard power supply by increasing the efficiency of thermal to electric conversion. In an RTPV, a radioisotope heats an emitter, which emits light to a photovoltaic (PV) cell, which converts the light into electricity. Developing an emitter tuned to the desired wavelength of the photovoltaic is a key part in increasing overall performance. Researchers at the NASA Glenn Research Center (GRC) have built a Thermal Photovoltaic (TPV) system, that utilizes a simulated General Purpose Heat Source (GPHS) from a MMRTG to heat a tantalum emitter. The GPHS is a block of graphite roughly 10 cm by 10 cm by 5 cm. A fully loaded GPHS produces 250 w of thermal power and weighs 1.6 kgs. The GRC system relies on the GPHS unit radiating at 1200 K to a tantalum emitter that, in turn, radiates light to a GaInAs photo-voltaic cell. The GRC claims system efficiency of conversion of 15%. The specific mass is around 167 kg/kWe. A RTPV power source that utilized a ceramic or ceramic-metal (cermet) matrix would allow for the combination of the heat source, canister, and emitter into one compact unit, and allow variation in size

  7. Emission of polycyclic aromatic hydrocarbons and their carcinogenic potencies from cooking sources to the urban atmosphere.

    PubMed Central

    Li, Chun-The; Lin, Yuan-Chung; Lee, Wen-Jhy; Tsai, Perng-Jy

    2003-01-01

    Traffic has long been recognized as the major contributor to polycyclic aromatic hydrocarbon (PAH) concentrations. However, this does not consider the contribution of cooking sources of PAHs. This study set out, first, to assess the characteristics of PAHs and their corresponding benzo[a]pyrene equivalent (B[a]Peq) emissions from cooking sources to the urban atmosphere. To illustrate the importance of cooking sources, PAH emissions from traffic sources were then calculated and compared. The entire study was conducted on a city located in southern Taiwan. PAH samples were collected from the exhaust stacks of four types of restaurant: Chinese, Western, fast food, and Japanese. For total PAHs, results show that the fractions of gaseous PAHs (range, 75.9-89.9%) were consistently higher than the fractions of particulate PAHs (range, 10.1-24.1%) in emissions from the four types of restaurant. But for total B[a]Peq, we found that the contributions of gaseous PAHs (range, 15.7-21.9%) were consistently lower than the contributions of particulate PAHs (range, 78.1-84.3%). For emission rates of both total PAHs and total B[a]Peq, a consistent trend was found for the four types of restaurant: Chinese (2,038 and 154 kg/year, respectively) > Western (258 and 20.4 kg/year, respectively) > fast food (31.4 and 0.104 kg/year, respectively) > Japanese (5.11 and 0.014 kg/year, respectively). By directly adapting the emission data obtained from Chinese restaurants, we found that emission rates on total PAHs and total B[a]Peq for home kitchen sources were 6,639 and 501 kg/year, respectively. By combining both restaurant sources and home kitchen sources, this study yielded emission rates of total PAHs and total B[a]Peq from cooking sources of the studied city of 8,973 and 675 kg/year, respectively. Compared with PAH emissions from traffic sources in the same city, we found that although the emission rates of total PAHs for cooking sources were significantly less than those for traffic

  8. Mapping methane sources and emissions over California from direct airborne flux and VOC source tracer measurements

    NASA Astrophysics Data System (ADS)

    Guha, A.; Misztal, P. K.; Peischl, J.; Karl, T.; Jonsson, H. H.; Woods, R. K.; Ryerson, T. B.; Goldstein, A. H.

    2013-12-01

    Quantifying the contributions of methane (CH4) emissions from anthropogenic sources in the Central Valley of California is important for validation of the statewide greenhouse gas (GHG) inventory and subsequent AB32 law implementation. The state GHG inventory is largely based on activity data and emission factor based estimates. The 'bottom-up' emission factors for CH4 have large uncertainties and there is a lack of adequate 'top-down' measurements to characterize emission rates. Emissions from non-CO2 GHG sources display spatial heterogeneity and temporal variability, and are thus, often, poorly characterized. The Central Valley of California is an agricultural and industry intensive region with large concentration of dairies and livestock operations, active oil and gas fields and refining operations, as well as rice cultivation all of which are known CH4 sources. In order to gain a better perspective of the spatial distribution of major CH4 sources in California, airborne measurements were conducted aboard a Twin Otter aircraft for the CABERNET (California Airborne BVOC Emissions Research in Natural Ecosystems Transects) campaign, where the driving research goal was to understand the spatial distribution of biogenic VOC emissions. The campaign took place in June 2011 and encompassed over forty hours of low-altitude and mixed layer airborne CH4 and CO2 measurements alongside coincident VOC measurements. Transects during eight unique flights covered much of the Central Valley and its eastern edge, the Sacramento-San Joaquin delta and the coastal range. We report direct quantification of CH4 fluxes using real-time airborne Eddy Covariance measurements. CH4 and CO2 were measured at 1-Hz data rate using an instrument based on Cavity Ring Down Spectroscopy (CRDS) along with specific VOCs (like isoprene, methanol, acetone etc.) measured at 10-Hz using Proton Transfer Reaction Mass Spectrometer - Eddy Covariance (PTRMS-EC) flux system. Spatially resolved eddy covariance

  9. The Power Source(s) of Nearby Low-Ionization Nuclear Emission Regions

    NASA Astrophysics Data System (ADS)

    Molina, Mallory; Eracleous, Michael; Maoz, Dan; Barth, Aaron J.; Walsh, Jonelle; Ho, Luis C.; Shields, Joseph C.

    2015-01-01

    The majority of low-ionization nuclear emission regions (LINERs) harbor supermassive black holes (SMBHs) with very low accretion rates. Since SMBHs spend most of their lifetimes in these low-accretion rate states, understanding LINERs is important for understanding active galactic nuclei (AGN) in the context of galaxy evolution. On scales of ~100 pc, the energy budget of LINERs appears to be deficient when the only source of power considered is the AGN. Thus, other energy sources are likely to contribute to the excitation of the emission-line gas. To probe these sources, we observed three nearby, bright LINERs, NGC 1052, NGC 4278 and NGC 4579, with the Space Telescope Imaging Spectrograph (STIS) on the Hubble Space Telescope (HST). We specifically looked at the 0.1-1 arcsecond (corresponding to 5-50 pc) scale to find what and how far from the nucleus these other energy sources are. After subtracting both the unresolved nuclear light and the spatially-extended starlight, we measured a number of diagnostic emission line ratios. We find that line ratios, such as [O III]/[O II] and [O III]/H-beta change as a function of distance from the nucleus. Within 5 pc, the line ratios suggest AGN photoionization. At larger distances the line ratios seem to be inconsistent with AGN photoionization, but they appear to be consistent with excitation by hot stars or shocks.

  10. Silicon Nanoparticles: Source of Extended Red Emission?

    NASA Astrophysics Data System (ADS)

    Witt, Adolf N.; Gordon, Karl D.; Furton, Douglas G.

    1998-07-01

    We have reviewed the characteristics of the extended red emission (ERE) as observed in many dusty astronomical environments, in particular, the diffuse interstellar medium of the Galaxy. The spectral nature and the photon conversion efficiency of the ERE identify the underlying process as highly efficient photoluminescence by an abundant component of interstellar dust. We have compared the photoluminescence properties of a variety of carbon- and silicon-based materials proposed as sources for the ERE with the observationally established constraints. We found that silicon nanoparticles provide the best match to the spectrum and to the efficiency requirement of the ERE. If present in interstellar space with an abundance sufficient to explain the intensity of the ERE, silicon nanoparticles will also contribute to the interstellar 9.7 μm Si--O stretch feature in absorption, to the near- and mid-IR nonequilibrium thermal background radiation, and to the continuum extinction in the near- and far-UV. About 36% of the interstellar silicon that is depleted into the dust phase would be needed in the form of silicon nanoparticles, amounting to less than 5% of the interstellar dust mass. We propose that silicon nanoparticles form through the nucleation of SiO in oxygen-rich stellar mass outflows and that they represent an important small-grain component of the interstellar dust spectrum.

  11. RESEARCH ON EMISSIONS AND MITIGATION OF POP'S FROM COMBUSTION SOURCES

    EPA Science Inventory

    Chapter summarizes EPA's research on emissions and control of persistent organic pollutants (POPS) from combustion sources, with emphasis on source characterization and measurement, formation and destruction mechanisms, formation prevention, and flue gas cleaning. Laboratory exp...

  12. RESEARCH ON EMISSIONS AND MITIGATION OF POP'S FROM COMBUSTION SOURCES

    EPA Science Inventory

    Chapter summarizes EPA's research on emissions and control of persistent organic pollutants (POPS) from combustion sources, with emphasis on source characterization and measurement, formation and destruction mechanisms, formation prevention, and flue gas cleaning. Laboratory exp...

  13. GAMMA DOSE RATE NEAR A NEW (252)Cf BRACHYTHERAPY SOURCE

    SciTech Connect

    Fortune, Eugene C; Gauld, Ian C; Wang, C

    2011-01-01

    A new generation of medical grade (252)Cf sources was developed in 2002 at the Oak Ridge National Laboratory. The combination of small size and large activity of (252)Cf makes the new source suitable to be used with the conventional high-dose-rate remote afterloading system for interstitial brachytherapy. A recent in-water calibration experiment showed that the measured gamma dose rates near the new source are slightly greater than the neutron dose rates, contradicting the well established neutron-to-gamma dose ratio of approximately 2:1 at locations near a (252)Cf brachytherapy source. Specifically, the MCNP-predicted gamma dose rate is a factor of two lower than the measured gamma dose rate at the distance of I cm, and the differences between the two results gradually diminish at distances farther away from the source. To resolve this discrepancy, we updated the source gamma spectrum by including in the ORIGEN-S data library the experimentally measured (252)Cf prompt gamma spectrum as well as the true (252)Cf spontaneous fission yield data to explicitly model delayed gamma emissions from fission products. We also investigated the bremsstrahlung X-rays produced by the beta particles emitted from fission product decays. The results show that the discrepancy of gamma dose rates is mainly caused by the omission of the bremsstrahlung X-rays in the MCNP runs. By including the bremsstrahlung X-rays, the MCNP results show that the gamma dose rates near a new (252)Cf source agree well with the measured results and that the gamma dose rates are indeed greater than the neutron dose rates.

  14. Estimating gas emissions from multiple sources using a backward Lagrangian stochastic model.

    PubMed

    Gao, Zhiling; Desjardins, Raymond L; van Haarlem, Ronald P; Flesch, Thomas K

    2008-11-01

    Manure storage tanks and animals in barns are important agricultural sources of methane. To examine the possibility of using an inverse dispersion technique based on a backward Lagrangian Stochastic (bLS) model to quantify methane (CH4) emissions from multiple on-farm sources, a series of tests were carried out with four possible source configurations and three controlled area sources. The simulated configurations were: (C1) three spatially separate ground-level sources, (C2) three spatially separate sources with wind-flow disturbance, (C3) three adjacent ground-level sources to simulate a group of adjacent sources with different emission rates, and (C4) a configuration with a ground level and two elevated sources. For multiple ground-level sources without flow obstructions (C1 and C3), we can use the condition number (K, the ratio of the uncertainty in the calculated emission rate to the uncertainty in the predicted ratio of concentration to emission rate) to evaluate the applicability of this inverse dispersion technique and a preliminary threshold of K <10 is recommended. For multiple sources with wind disturbance (C2) or an even more complex configuration including ground level and elevated sources (C4), a low kappa is not sufficient to provide reasonable discrete and total emission rates. The effect of flow obstructions can be neglected as long as the distance between the source and the measurement location is greater than approximately 10 times the height of the flow obstructions. This study shows that the bLS model has the potential to provide accurate discrete emission rates from multiple on-farm emissions of gases provided that certain conditions are met.

  15. Atmospheric measurement of point source fossil CO2 emissions

    NASA Astrophysics Data System (ADS)

    Turnbull, J. C.; Keller, E. D.; Baisden, T.; Brailsford, G.; Bromley, T.; Norris, M.; Zondervan, A.

    2014-05-01

    We use the Kapuni Gas Treatment Plant to examine methodologies for atmospheric monitoring of point source fossil fuel CO2 (CO2ff) emissions. The Kapuni plant, located in rural New Zealand, removes CO2 from locally extracted natural gas and vents that CO2 to the atmosphere, at a rate of ~0.1 Tg carbon per year. The plant is located in a rural dairy farming area, with no other significant CO2ff sources nearby, but large, diurnally varying, biospheric CO2 fluxes from the surrounding highly productive agricultural grassland. We made flask measurements of CO2 and 14CO2 (from which we derive the CO2ff component) and in situ measurements of CO2 downwind of the Kapuni plant, using a Helikite to sample transects across the emission plume from the surface up to 100 m above ground level. We also determined the surface CO2ff content averaged over several weeks from the 14C content of grass samples collected from the surrounding area. We use the WindTrax plume dispersion model to compare the atmospheric observations with the emissions reported by the Kapuni plant, and to determine how well atmospheric measurements can constrain the emissions. The model has difficulty accurately capturing the fluctuations and short-term variability in the Helikite samples, but does quite well in representing the observed CO2ff in 15 min averaged surface flask samples and in ~ one week integrated CO2ff averages from grass samples. In this pilot study, we found that using grass samples, the modeled and observed CO2ff emissions averaged over one week agreed to within 30%. The results imply that greater verification accuracy may be achieved by including more detailed meteorological observations and refining 14C sampling strategies.

  16. Atmospheric measurement of point source fossil fuel CO2 emissions

    NASA Astrophysics Data System (ADS)

    Turnbull, J. C.; Keller, E. D.; Baisden, W. T.; Brailsford, G.; Bromley, T.; Norris, M.; Zondervan, A.

    2013-11-01

    We use the Kapuni Gas Treatment Plant to examine methodologies for atmospheric monitoring of point source fossil fuel CO2 (CO2ff) emissions. The Kapuni plant, located in rural New Zealand, removes CO2 from locally extracted natural gas and vents that CO2 to the atmosphere, at a rate of ~0.1 Tg carbon per year. The plant is located in a rural dairy farming area, with no other significant CO2ff sources nearby, but large, diurnally varying, biospheric CO2 fluxes from the surrounding highly productive agricultural grassland. We made flask measurements of CO2 and 14CO2 (from which we derive the CO2ff component) and in situ measurements of CO2 downwind of the Kapuni plant, using a Helikite to sample transects across the emission plume from the surface up to 100 m a.g.l. We also determined the surface CO2ff content averaged over several weeks from the 14CO2 content of grass samples collected from the surrounding area. We use the WindTrax plume dispersion model to compare the atmospheric observations with the emissions reported by the Kapuni plant, and to determine how well atmospheric measurements can constrain the emissions. The model has difficulty accurately capturing the fluctuations and short-term variability in the Helikite samples, but does quite well in representing the observed CO2ff in 15 min averaged surface flask samples and in ~1 week integrated CO2ff averages from grass samples. In this pilot study, we found that using grass samples, the modeled and observed CO2ff emissions averaged over one week agreed to within 30%. The results imply that greater verification accuracy may be achieved by including more detailed meteorological observations and refining 14CO2 sampling strategies.

  17. N-bursty emission from Uranus: A cyclotron maser source?

    NASA Technical Reports Server (NTRS)

    Curran, D. B.; Menietti, J. D.

    1993-01-01

    Ray tracing studies of RX-mode emission from the north polar regions of Uranus indicate that the n-bursty radio emission may have a source along field lines with footprints near the northern magnetic pole (perhaps in the cusp), but not necessarily associated with regions of strong UV emission. This is in contrast with similar studies for the Uranus nightside smooth radio emission, which are believed to be due to the cyclotron maser instability. Source regions can be found for both hollow and filled emission cones and for frequencies well above the local gyrofreuquency implying that mechanisms other than the cyclotron maser mechanism may be operating.

  18. Locating and estimating air emissions from sources of epichlorohydrin

    SciTech Connect

    Not Available

    1985-09-01

    To assist groups interested in inventorying air emissions of various potentially toxic substances, EPA is preparing a series of documents such as this to compile available information on sources and emissions of these substances. This document deals specifically with epichlorohydrin. Its intended audience includes Federal, State and local air pollution personnel and others interested in locating potential emitters of epichlorohydrin in making gross estimates of air emissions therefrom. This document presents information on 1) the types of sources that may emit epichlorohydrin; 2) process variations and release points that may be expected within these sources; and 3) available emissions information indicating the potential for epichlorohydrin release into the air from each operation.

  19. Locating and estimating air emissions from sources of phosgene

    SciTech Connect

    Not Available

    1985-09-01

    To assist groups interested in inventorying air emissions of various potentially toxic substances, EPA is preparing a series of documents such as this to compile available information on sources and emissions of these substances. This document deals specifically with phosgene. Its intended audience includes Federal, State and local air pollution personnel and others interested in locating potential emitters of phosgene in making gross estimates of air emissions therefrom. This document presents information on (1) the types of sources that may emit phosgene, (2) process variations and release points that may be expected within these sources, and (3) available emissions information indicating the potential for phosgene release into the air from each operation.

  20. Source sampling of particulate matter emissions from cotton harvesting - System field testing and emission factor development

    USDA-ARS?s Scientific Manuscript database

    Emission factors are used in the air pollution regulatory process to quantify the mass of pollutants emitted from a source. Accurate emission factors must be used in the air pollution regulatory process to ensure fair and appropriate regulation for all sources. Agricultural sources, including cotton...

  1. Area Source Emission Measurements Using EPA OTM 10

    EPA Science Inventory

    Measurement of air pollutant emissions from area and non-point sources is an emerging environmental concern. Due to the spatial extent and non-homogenous nature of these sources, assessment of fugitive emissions using point sampling techniques can be difficult. To help address th...

  2. 40 CFR 62.4622 - Emission inventories, source surveillance, reports.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 8 2010-07-01 2010-07-01 false Emission inventories, source surveillance, reports. 62.4622 Section 62.4622 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY...) § 62.4622 Emission inventories, source surveillance, reports. (a) The requirements of § 60.25(a) of...

  3. 40 CFR 62.4622 - Emission inventories, source surveillance, reports.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 8 2011-07-01 2011-07-01 false Emission inventories, source surveillance, reports. 62.4622 Section 62.4622 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY...) § 62.4622 Emission inventories, source surveillance, reports. (a) The requirements of § 60.25(a) of...

  4. 40 CFR 62.4622 - Emission inventories, source surveillance, reports.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 9 2014-07-01 2014-07-01 false Emission inventories, source surveillance, reports. 62.4622 Section 62.4622 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY...) § 62.4622 Emission inventories, source surveillance, reports. (a) The requirements of § 60.25(a) of...

  5. 40 CFR 62.4622 - Emission inventories, source surveillance, reports.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 9 2012-07-01 2012-07-01 false Emission inventories, source surveillance, reports. 62.4622 Section 62.4622 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY...) § 62.4622 Emission inventories, source surveillance, reports. (a) The requirements of § 60.25(a) of...

  6. 40 CFR 62.4622 - Emission inventories, source surveillance, reports.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 9 2013-07-01 2013-07-01 false Emission inventories, source surveillance, reports. 62.4622 Section 62.4622 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY...) § 62.4622 Emission inventories, source surveillance, reports. (a) The requirements of § 60.25(a) of...

  7. Area Source Emission Measurements Using EPA OTM 10

    EPA Science Inventory

    Measurement of air pollutant emissions from area and non-point sources is an emerging environmental concern. Due to the spatial extent and non-homogenous nature of these sources, assessment of fugitive emissions using point sampling techniques can be difficult. To help address th...

  8. REVIEW OF INDOOR EMISSION SOURCE MODELS--PART 1. OVERVIEW

    EPA Science Inventory

    Indoor emission source models are mainly used as a component in indoor air quality (IAQ) and exposure modeling. They are also widely used to interpret the experimental data obtained from environmental chambers and buildings. This paper compiles 46 indoor emission source models fo...

  9. Statistics of Isolated Emission Sources in Cataclysmic Variables

    NASA Astrophysics Data System (ADS)

    Tappert, C.; Hanuschik, R.

    The strong emission lines in cataclysmic variables are the primary source of information on physical parameters of and the accretion process in these systems. Many examples show that the lines are composed not only from (symmetrical) disc emission, but that additional contribution is provided by isolated, i.e. asymmetric emission sources, distorting the original line profile. In this paper, we study the distribution of these additional components with several system parameters.

  10. 75 FR 63259 - Standards of Performance for New Stationary Sources and Emission Guidelines for Existing Sources...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-10-14

    ... performance tests would ensure that emission factors, when updated, represent accurately the most current... Protection Agency 40 CFR Part 60 Standards of Performance for New Stationary Sources and Emission Guidelines... Part 60 RIN 2060-AP90 Standards of Performance for New Stationary Sources and Emission Guidelines for...

  11. Registration for the Hanford Site: Sources of radioactive emissions

    SciTech Connect

    Silvia, M.J.

    1993-04-01

    This Registration Application serves to renew the registration for all Hanford Site sources of radioactive air emissions routinely reported to the State of Washington Department of Health (DOH). The current registration expires on August 15, 1993. The Application is submitted pursuant to the Washington Administrative Code (WAC) Chapter 246--247, and is consistent with guidance provided by DOH for renewal. The Application subdivides the Hanford Site into six major production, processing or research areas. Those six areas are in the 100 Area, 200 East Area, 200 West Area, 300 Area, 400 Area, and 600 Area. Each major group of point sources within the six areas listed above is represented by a Source Registration for Radioactive Air Emissions form. Annual emissions. for the sources are listed in the ``Radionuclide Air Emissions Report for the Hanford Site,`` published annually. It is a requirement that the following Statement of Compliance be provided: ``The radioactive air emissions from the above sources do meet the emissions standards contained in Chapter 173-480-040 WAC, Ambient Air Quality Standards and Emissions Limits for Radionuclides. As the Statement of Compliance pertains to this submittal, the phrase ``above sources`` is to be understood as meaning the combined air emissions from all sources registered by this submittal.

  12. Russia's black carbon emissions: focus on diesel sources

    DOE PAGES

    Kholod, Nazar; Evans, Meredydd; Kuklinski, Teresa

    2016-09-12

    Black carbon (BC) is a significant climate forcer with a particularly pronounced forcing effect in polar regions such as the Russian Arctic. Diesel combustion is a major global source of BC emissions, accounting for 25–30 % of all BC emissions. While the demand for diesel is growing in Russia, the country's diesel emissions are poorly understood. This paper presents a detailed inventory of Russian BC emissions from diesel sources. Drawing on a complete Russian vehicle registry with detailed information about vehicle types and emission standards, this paper analyzes BC emissions from diesel on-road vehicles. We use the COPERT emission modelmore » (COmputer Programme to calculate Emissions from Road Transport) with Russia-specific emission factors for all types of on-road vehicles. On-road diesel vehicles emitted 21 Gg of BC in 2014: heavy-duty trucks account for 60% of the on-road BC emissions, while cars represent only 5% (light commercial vehicles and buses account for the remainder). Using Russian activity data and fuel-based emission factors, the paper also presents BC emissions from diesel locomotives and ships, off-road engines in industry, construction and agriculture, and generators. The study also factors in the role of superemitters in BC emissions from diesel on-road vehicles and off-road sources. The total emissions from diesel sources in Russia are estimated to be 49 Gg of BC and 17 Gg of organic carbon (OC) in 2014. Off-road diesel sources emitted 58% of all diesel BC in Russia.« less

  13. Russia's black carbon emissions: focus on diesel sources

    SciTech Connect

    Kholod, Nazar; Evans, Meredydd; Kuklinski, Teresa

    2016-09-12

    Black carbon (BC) is a significant climate forcer with a particularly pronounced forcing effect in polar regions such as the Russian Arctic. Diesel combustion is a major global source of BC emissions, accounting for 25–30 % of all BC emissions. While the demand for diesel is growing in Russia, the country's diesel emissions are poorly understood. This paper presents a detailed inventory of Russian BC emissions from diesel sources. Drawing on a complete Russian vehicle registry with detailed information about vehicle types and emission standards, this paper analyzes BC emissions from diesel on-road vehicles. We use the COPERT emission model (COmputer Programme to calculate Emissions from Road Transport) with Russia-specific emission factors for all types of on-road vehicles. On-road diesel vehicles emitted 21 Gg of BC in 2014: heavy-duty trucks account for 60% of the on-road BC emissions, while cars represent only 5% (light commercial vehicles and buses account for the remainder). Using Russian activity data and fuel-based emission factors, the paper also presents BC emissions from diesel locomotives and ships, off-road engines in industry, construction and agriculture, and generators. The study also factors in the role of superemitters in BC emissions from diesel on-road vehicles and off-road sources. The total emissions from diesel sources in Russia are estimated to be 49 Gg of BC and 17 Gg of organic carbon (OC) in 2014. Off-road diesel sources emitted 58% of all diesel BC in Russia.

  14. Russia's black carbon emissions: focus on diesel sources

    NASA Astrophysics Data System (ADS)

    Kholod, Nazar; Evans, Meredydd; Kuklinski, Teresa

    2016-09-01

    Black carbon (BC) is a significant climate forcer with a particularly pronounced forcing effect in polar regions such as the Russian Arctic. Diesel combustion is a major global source of BC emissions, accounting for 25-30 % of all BC emissions. While the demand for diesel is growing in Russia, the country's diesel emissions are poorly understood. This paper presents a detailed inventory of Russian BC emissions from diesel sources. Drawing on a complete Russian vehicle registry with detailed information about vehicle types and emission standards, this paper analyzes BC emissions from diesel on-road vehicles. We use the COPERT emission model (COmputer Programme to calculate Emissions from Road Transport) with Russia-specific emission factors for all types of on-road vehicles. On-road diesel vehicles emitted 21 Gg of BC in 2014: heavy-duty trucks account for 60 % of the on-road BC emissions, while cars represent only 5 % (light commercial vehicles and buses account for the remainder). Using Russian activity data and fuel-based emission factors, the paper also presents BC emissions from diesel locomotives and ships, off-road engines in industry, construction and agriculture, and generators. The study also factors in the role of superemitters in BC emissions from diesel on-road vehicles and off-road sources. The total emissions from diesel sources in Russia are estimated to be 49 Gg of BC and 17 Gg of organic carbon (OC) in 2014. Off-road diesel sources emitted 58 % of all diesel BC in Russia.

  15. Russia's black carbon emissions: focus on diesel sources

    SciTech Connect

    Kholod, Nazar; Evans, Meredydd; Kuklinski, Teresa

    2016-01-01

    Black carbon (BC) is a significant climate forcer with a particularly pronounced forcing effect in polar regions such as the Russian Arctic. Diesel combustion is a major global source of BC emissions, accounting for 25–30% of all BC emissions. While the demand for diesel is growing in Russia, the country's diesel emissions are poorly understood. This paper presents a detailed inventory of Russian BC emissions from diesel sources. Drawing on a complete Russian vehicle registry with detailed information about vehicle types and emission standards, this paper analyzes BC emissions from diesel on-road vehicles. We use the COPERT emission model (COmputer Programme to calculate Emissions from Road Transport) with Russia-specific emission factors for all types of on-road vehicles. On-road diesel vehicles emitted 21 Gg of BC in 2014: heavy-duty trucks account for 60% of the on-road BC emissions, while cars represent only 5% (light commercial vehicles and buses account for the remainder). Using Russian activity data and fuel-based emission factors, the paper also presents BC emissions from diesel locomotives and ships, off-road engines in industry, construction and agriculture, and generators. The study also factors in the role of superemitters in BC emissions from diesel on-road vehicles and off-road sources. The total emissions from diesel sources in Russia are estimated to be 49 Gg of BC and 17 Gg of organic carbon (OC) in 2014. Off-road diesel sources emitted 58% of all diesel BC in Russia.

  16. REGIONAL ASSESSMENT OF METHANE EMISSION RATES FROM RESERVOIRS IN THE MIDWESTERN UNITED STATES

    EPA Science Inventory

    Reservoirs are a globally significant source of methane (CH4) to the atmosphere, but regional and global emission estimates are poorly constrained due to high variability in emission rates among reservoirs and a lack of measurements in some areas geographic areas. Methane emissi...

  17. REGIONAL ASSESSMENT OF METHANE EMISSION RATES FROM RESERVOIRS IN THE MIDWESTERN UNITED STATES

    EPA Science Inventory

    Reservoirs are a globally significant source of methane (CH4) to the atmosphere, but regional and global emission estimates are poorly constrained due to high variability in emission rates among reservoirs and a lack of measurements in some areas geographic areas. Methane emissi...

  18. Setting maximum emission rates from ozone emitting consumer appliances in the United States and Canada

    NASA Astrophysics Data System (ADS)

    Morrison, Glenn; Shaughnessy, Richard; Shu, Shi

    2011-02-01

    A Monte Carlo analysis of indoor ozone levels in four cities was applied to provide guidance to regulatory agencies on setting maximum ozone emission rates from consumer appliances. Measured distributions of air exchange rates, ozone decay rates and outdoor ozone levels at monitoring stations were combined with a steady-state indoor air quality model resulting in emission rate distributions (mg h -1) as a function of % of building hours protected from exceeding a target maximum indoor concentration of 20 ppb. Whole-year, summer and winter results for Elizabeth, NJ, Houston, TX, Windsor, ON, and Los Angeles, CA exhibited strong regional differences, primarily due to differences in air exchange rates. Infiltration of ambient ozone at higher average air exchange rates significantly reduces allowable emission rates, even though air exchange also dilutes emissions from appliances. For Houston, TX and Windsor, ON, which have lower average residential air exchange rates, emission rates ranged from -1.1 to 2.3 mg h -1 for scenarios that protect 80% or more of building hours from experiencing ozone concentrations greater than 20 ppb in summer. For Los Angeles, CA and Elizabeth, NJ, with higher air exchange rates, only negative emission rates were allowable to provide the same level of protection. For the 80th percentile residence, we estimate that an 8-h average limit concentration of 20 ppb would be exceeded, even in the absence of an indoor ozone source, 40 or more days per year in any of the cities analyzed. The negative emission rates emerging from the analysis suggest that only a zero-emission rate standard is prudent for Los Angeles, Elizabeth, NJ and other regions with higher summertime air exchange rates. For regions such as Houston with lower summertime air exchange rates, the higher emission rates would likely increase occupant exposure to the undesirable products of ozone reactions, thus reinforcing the need for zero-emission rate standard.

  19. Black carbon emissions from diesel sources in Russia. Final report

    SciTech Connect

    Kholod, Nazar; Evans, Meredydd

    2016-08-31

    This report presents a detailed inventory of Russian BC emissions from diesel sources. Drawing on a complete Russian vehicle registry with detailed information about vehicle types and emission standards, this report analyzes BC emissions from diesel on-road vehicles. On-road diesel vehicles emitted 21 Gg of BC in 2014: heavy-duty trucks account for 60% of the on-road BC emissions, while cars represent only 5% (light commercial vehicles and buses account for the remainder). Using Russian activity data and fuel-based emission factors, the report also presents BC emissions from diesel locomotives and ships, off-road engines in industry, construction and agriculture, and generators. The total emissions from diesel sources in Russia are estimated to be 49 Gg of BC in 2014.

  20. Characterization of emissions from combustion sources: controlled studies

    SciTech Connect

    Tucker, W.G.

    1987-01-01

    This paper summarizes Session I papers (given at the EPA Workshop on Characterization of Contaminant Emissions from Indoor Sources, Chapel Hill, NC, May 1985) that illustrate the progress made to date on characterizing indoor-combustion emissions from unvented space heaters, gas appliances, and sidestream cigarette smoke. The state of knowledge of such emissions and their controllability is summarized by four general statements: (1) Unvented gas-fired appliances are important sources of indoor CO and NOx, but not of organic emissions; (2) Important combustion sources of indoor organics, include smoking and possibly kerosene heaters; (3) The extent of the problems of leakage from vented appliances is simply not known; (4) Indoor combustion sources do not appear to present major problems with controllability, if source removal is an acceptable alternative. From an engineering standpoint, the most-challenging issue is burner design changes for unvented appliances.

  1. 40 CFR 1036.530 - Calculating greenhouse gas emission rates.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 33 2014-07-01 2014-07-01 false Calculating greenhouse gas emission rates. 1036.530 Section 1036.530 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Procedures § 1036.530 Calculating greenhouse gas emission rates. This section describes how to...

  2. 40 CFR 1036.530 - Calculating greenhouse gas emission rates.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 34 2012-07-01 2012-07-01 false Calculating greenhouse gas emission rates. 1036.530 Section 1036.530 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Procedures § 1036.530 Calculating greenhouse gas emission rates. This section describes how to...

  3. 40 CFR 1036.530 - Calculating greenhouse gas emission rates.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 34 2013-07-01 2013-07-01 false Calculating greenhouse gas emission rates. 1036.530 Section 1036.530 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Procedures § 1036.530 Calculating greenhouse gas emission rates. This section describes how to...

  4. Emissions from laboratory combustion of wildland fuels: Emission factors and source profiles

    Treesearch

    L.-W. Anthony Chen; Hans Moosmuller; W. Patrick Arnott; Judith C. Chow; John G. Watson; Ronald A. Susott; Ronald E. Babbitt; Cyle E. Wold; Emily N. Lincoln; Wei Min Hao

    2007-01-01

    Combustion of wildland fuels represents a major source of particulate matter (PM) and light-absorbing elemental carbon (EC) on a national and global scale, but the emission factors and source profiles have not been well characterized with respect to different fuels and combustion phases. These uncertainties limit the accuracy of current emission inventories, smoke...

  5. 40 CFR 74.22 - Actual SO2 emissions rate.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...: SO2 Emissions Factor = (average percent of sulfur by weight) × (k), where, average percent of sulfur by weight = annual average, for a combustion source submitting annual data = monthly average, for a...” is as defined under § 74.20(a)(2)(i); “SO2 emissions factor” is as defined under paragraph (b) of...

  6. Field Measurements of Isoprene and Monoterpene Emission Rates from Trees.

    NASA Astrophysics Data System (ADS)

    Dilts, Stephen Blair

    Monoterpene emission rates were measured by a branch enclosure technique from Pinus ponderosa in central Oregon in the early summer and fall along with photosynthesis and monoterpene needle concentrations. beta -pinene, Delta^3-carene, and alpha-pinene were the major constituents of the emissions with smaller amounts of myrcene, limonene, and beta-phellandrene. The emission rates of alpha-pinene and beta-pinene were highly correlated with their needle concentrations, while those of Delta ^3-carene were not. There was no discernible effect on emissions when photosynthesis was water stress limited in the fall, and monoterpene emissions appear to be distinct from short term photosynthetic carbon assimilation. Isoprene emission rates were measured from a Quercus robur on the Washington State University campus in the fall of 1989 and throughout the 1990 growing season, and from a Quercus rubra during most of the 1991 season and occasionally in 1992. The measured emission rates showed distinct seasonal patterns which could not be explained by temperature or light. Emission rates were initially low early in the season when the leaves were immature. Rates increased rapidly after leaf maturity to a maximum value and then declined over the rest of the season. Evidence suggests that the rate and magnitude of this decline depends on stresses on the tree. Isoprene emission rates were measured from several species near Oak Ridge, Tennessee. The mean normalized isoprene emission rate from the branch enclosure was compared to the rate measured from a Q. alba leaf in a light and temperature controlled cuvette. The branch enclosure result for Q. alba was about 65% lower than the mean leaf cuvette measurement. This difference appears be due to shading of leaves within the branch enclosure. A comparison was also made between the normalized branch enclosure results and normalized canopy isoprene flux measured by a micrometeorological gradient method with generally good agreement.

  7. Calculated emission rates for barium releases in space

    NASA Technical Reports Server (NTRS)

    Stenbaek-Nielsen, H. C.

    1989-01-01

    The optical emissions from barium releases in space are caused by resonance and fluorescent scattering of sunlight. Emission rates for the dominant ion and neutral lines are calculated assuming the release to be optically thin and the barium to be in radiative equilibrium with the solar radiation. The solar spectrum has deep Fraunhofer absorption lines at the primary barium ion resonances. A velocity component toward or away from the sun will Doppler shift the emission lines relative to the absorption lines and the emission rates will increase many-fold over the rest value. The Doppler brightening is important in shaped charge or satellite releases where the barium is injected at high velocities. Emission rates as a function of velocity are calculated for the 4554, 4934, 5854, 6142 and 6497 A ion emission lines and the dominant neutral line at 5535 A. Results are presented for injection parallel to the ambient magnetic field, B, and for injection at an angle to B.

  8. User access to the MAP3S source emissions inventory

    SciTech Connect

    Benkovitz, C M; Evans, V A

    1981-03-01

    An emissions inventory based on data obtained from the National Emissions Data System (NEDS), the Federal Power Commission (FPC), Environment Canada, and other agencies was compiled by the MAP3S Central Data Coordination at Brookhaven National Laboratory. Pertinent data was brought together, collated, and loaded into computerized data bases using SYSTEM 2000 as the data base management system. These data bases are available to interested users for interactive scanning or batch retrieval. The emissions inventory consists of two distinct sections: a point source inventory and an area source inventory. The point source inventory covers the continental US and Canada; information is kept at the individual source level. The area source inventory covers the continental US; information is kept on a county basis. Work is in progress to obtain a Canadian area source inventory based on census divisions.

  9. High dose rate brachytherapy source measurement intercomparison.

    PubMed

    Poder, Joel; Smith, Ryan L; Shelton, Nikki; Whitaker, May; Butler, Duncan; Haworth, Annette

    2017-06-01

    This work presents a comparison of air kerma rate (AKR) measurements performed by multiple radiotherapy centres for a single HDR (192)Ir source. Two separate groups (consisting of 15 centres) performed AKR measurements at one of two host centres in Australia. Each group travelled to one of the host centres and measured the AKR of a single (192)Ir source using their own equipment and local protocols. Results were compared to the (192)Ir source calibration certificate provided by the manufacturer by means of a ratio of measured to certified AKR. The comparisons showed remarkably consistent results with the maximum deviation in measurement from the decay-corrected source certificate value being 1.1%. The maximum percentage difference between any two measurements was less than 2%. The comparisons demonstrated the consistency of well-chambers used for (192)Ir AKR measurements in Australia, despite the lack of a local calibration service, and served as a valuable focal point for the exchange of ideas and dosimetry methods.

  10. 40 CFR 63.1157 - Emission standards for existing sources.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Facilities and Hydrochloric Acid Regeneration Plants § 63.1157 Emission standards for existing sources. (a... percent. (b) Hydrochloric acid regeneration plants. (1) No owner or operator of an existing affected plant...

  11. Satellite-derived emissions inventories and detection of missing sources

    NASA Astrophysics Data System (ADS)

    McLinden, C. A.; Fioletov, V.; Shephard, M.; Krotkov, N. A.; Li, C.; Joiner, J.

    2016-12-01

    Our understanding of the impacts of air pollution on health and the environment, and our ability to predict future levels, is limited by our knowledge of its sources. Here, a global inventory of SO2 emissions, derived from the Ozone Monitoring Instrument (OMI) on the Aura satellite and independent of conventional emissions databases, is presented. Our OMI-based inventory is found to be generally consistent with these conventional inventories. However, since we are also able to detect emission sources (in addition to quantifying their emissions), many SO2 sources were identified that are evidently missing from bottom-up inventories, including nearly 40 large anthropogenic sources pointing to significant discrepancies in some regions such as the Middle-East. The methodology, inventory highlights, and applications to other pollutants (NO2 from OMI and NH3 from the Cross-track Infrared Sounder) will be discussed.

  12. Ammonia emissions from non-agricultural sources in the UK

    NASA Astrophysics Data System (ADS)

    Sutton, M. A.; Dragosits, U.; Tang, Y. S.; Fowler, D.

    A detailed literature review has been undertaken of the magnitude of non-agricultural sources of ammonia (NH 3) in the United Kingdom. Key elements of the work included estimation of nitrogen (N) excreted by different sources (birds, animals, babies, human sweat), review of miscellaneous combustion sources, as well as identification of industrial sources and use of NH 3 as a solvent. Overall the total non-agricultural emission of NH 3 from the UK in 1996 is estimated here as 54 (27-106) kt NH 3-N yr -1, although this includes 11 (6-23) kt yr -1 from agriculture related sources (sewage sludge spreading, biomass burning and agro-industry). Compared with previous estimates for 1990, component source magnitudes have changed both because of revised average emissions per source unit (emission factors) and changes in the source activity between 1990 and 1996. Sources with larger average emission factors than before include horses, wild animals and sea bird colonies, industry, sugar beet processing, household products and non-agricultural fertilizer use, with the last three sources being included for the first time. Sources with smaller emission factors than before include: land spreading of sewage sludge, direct human emissions (sweat, breath, smoking, infants), pets (cats and dogs) and fertilizer manufacture. Between 1990 and 1996 source activities increased for sewage spreading (due to reduced dumping at sea) and transport (due to increased use of catalytic converters), but decreased for coal combustion. Combined with the current UK estimates of agricultural NH 3 emissions of 229 kt N yr -1 (1996), total UK NH 3 emissions are estimated at 283 kt N yr -1. Allowing for an import of reduced nitrogen (NH x) of 30 kt N yr -1 and deposition of 230 kt N yr -1, these figures imply an export of 83 kt NH 3-N yr -1. Although export is larger than previously estimated, due to the larger contribution of non-agricultural NH 3 emissions, it is still insufficient to balance the UK

  13. Determination of methane emission rates on a biogas plant using data from laser absorption spectrometry.

    PubMed

    Groth, Angela; Maurer, Claudia; Reiser, Martin; Kranert, Martin

    2015-02-01

    The aim of the work was to establish a method for emission control of biogas plants especially the observation of fugitive methane emissions. The used method is in a developmental stage but the topic is crucial to environmental and economic issues. A remote sensing measurement method was adopted to determine methane emission rates of a biogas plant in Rhineland-Palatinate, Germany. An inverse dispersion model was used to deduce emission rates. This technique required one concentration measurement with an open path tunable diode laser absorption spectrometer (TDLAS) downwind and upwind the source and basic wind information, like wind speed and direction. Different operating conditions of the biogas plant occurring on the measuring day (December 2013) could be represented roughly in the results. During undisturbed operational modes the methane emission rate averaged 2.8 g/s, which corresponds to 4% of the methane gas production rate of the biogas plant. Copyright © 2014 Elsevier Ltd. All rights reserved.

  14. Atmospheric Verification of Point Source Fossil Fuel CO2 Emissions

    NASA Astrophysics Data System (ADS)

    Turnbull, J. C.; Keller, E. D.; Norris, M. W.; Wiltshire, R.; Baisden, W. T.; Brailsford, G. W.; Bromley, T.

    2015-12-01

    Large point sources (electricity generation and large-scale industry) make up roughly one third of all fossil fuel CO2 (CO2ff) emissions. Currently, these emissions are determined from self-reported inventory data, and sometimes from smokestack emissions monitoring, and the uncertainty in emissions from individual power plants is about 20%. We examine the utility of atmospheric 14C measurements combined with atmospheric transport modelling as a tool for independently quantifying point source CO2ff emissions, to both improve the accuracy of the reported emissions and for verification as we move towards a regulatory environment. We use the Kapuni Gas Treatment Facility as a test case. It is located in rural New Zealand with no other significant fossil fuel CO2 sources nearby, and emits CO2ff at ~0.1 Tg carbon per year. We use several different sampling methods to determine the 14C and hence the CO2ff content downwind of the emission source: grab flask samples of whole air; absorption of CO2 into sodium hydroxide integrated over many hours; and plant material which faithfully records the 14C content of assimilated CO2. We use a plume dispersion model to compare the reported emissions with our observed CO2ff mole fractions. We show that the short-term variability in plume dispersion makes it difficult to interpret the grab flask sample results, whereas the variability is averaged out in the integrated samples and we obtain excellent agreement between the reported and observed emissions, indicating that the 14C method can reliably be used to evaluated point source emissions.

  15. Effect of carbon sources on nitrous oxide emission in a modified Ludzak Ettinger process.

    PubMed

    Song, Kang; Riya, Shohei; Hosomi, Masaaki; Terada, Akihiko

    2015-01-01

    Effect of methanol and glycerol on nitrous oxide (N2O) emission in two laboratory-scale modified Ludzak Ettinger (MLE) processes was investigated during three distinct periods: dissolved oxygen (DO) control by intermittent aeration with a DO controller, and high and low aeration rates. N2O consumption rate in an anoxic tank and aeration mode influenced N2O emission rates from the MLE processes. In the DO control period, N2O emission rate from the glycerol-fed MLE process was higher than the methanol-fed counterpart, likely caused by a higher N2O consumption rate in an anoxic tank of the methanol-fed process. During the period of a higher aeration rate, N2O emission rates from both processes were comparable. In contrast, during the period of a lower aeration rate, N2O emission rate from the methanol-fed MLE process was higher than that from the glycerol-fed counterpart likely because of a higher degree of nitrite accumulation, corroborated by statistical analysis. N2O consumption activities of biomasses fed with the different carbon sources were distinct. However, the high activity did not necessarily result in a decrease in N2O emission rate from an aerobic tank and the effect of nitrite on the emission was stronger under the tested conditions.

  16. Dust from southern Africa: rates of emission and biogeochemical properties

    NASA Astrophysics Data System (ADS)

    Bhattachan, A.; D'Odorico, P.; Zobeck, T. M.; Okin, G. S.; Dintwe, K.

    2012-12-01

    The stabilized linear dunefields in the southern Kalahari show signs of reactivation due to reduced vegetation cover owing to drought and/or overgrazing. It has been demonstrated with a laboratory dust generator that the southern Kalahari soils are good emitters of dust and that large-scale dune reactivation can potentially make the region an important dust source in the relatively low-dust Southern Hemisphere. We show that emergence of the southern Kalahari as a new dust source may affect ocean biogeochemistry as the soils are rich in soluble iron and the dust from the southern Kalahari commonly reaches the Southern Ocean. We investigate the biogeochemical properties of the fine fraction of soil from the Kalahari dunes and compare them to those of currently active dust sources such as the Makgadikgadi and the Etosha pans as well as other smaller pans in the region. Using field measurements of sediment fluxes and satellite images, we calculate the rates of dust emission from the southern Kalahari under different land cover scenarios. To assess the reversibility of dune reactivation in the southern Kalahari, we investigate the resilience of dunefield vegetation by looking at changes in soil nutrients, fine soil fractions, and seed bank in areas affected by intense denudation.

  17. [Odor emission rate of municipal solid waste from landfill working area].

    PubMed

    Qiang, Ning; Wang, Hong-Yu; Zhao, Ai-Hua; Yuan, Wen-Xiang; Tai, Jun; Chen, Meng

    2014-02-01

    Emission rates of volatile organic compounds (VOCs), H2S and odor unit from the surface of a municipal solid waste (MSW) landfill working area were measured with a wind tunnel sampler. The results show that the emission rate of odor from the non-point source of landfill is the function of environmental temperature and surface sweeping velocity. The emission rate measured in the high temperature season can be 6 times higher of that in the low temperature season. Within the experimental range of 0.6-4 m x s(-1) wind sweeping velocity, the emission rate shows a linear relationship with wind sweeping velocity. In summer, the emission rates of VOCs (measured by PID as isobutylene), H2S and odor unit are 385-680 microg x (m(2) x s)(-1), 4-7 microg x (m(2) x s)(-1), and 46.5-136 OU x (m(2) x s)(-1) respectively. The continuous sweeping experiment shows that the emission rate measured with clean air sweeping is the maximum possible emission rate, which needs to be adjusted when it is used to estimate the odor concentration of more than 10 min sample time or an area emission load.

  18. Global inventory of volatile organic compound emissions from anthropogenic sources

    SciTech Connect

    Piccot, S.D.; Watson, J.J.; Jones, J.W.

    1992-01-01

    The paper discusses the development of a global inventory of anthropogenic volatile organic compound (VOC) emissions. It includes VOC estimates for seven classes of VOCs: paraffins, olefins, aromatics (benzene, toluene, xylene), formaldehyde, other aldehydes, other aromatics, and marginally reactive compounds. These classes represent general classes of VOC compounds that possess different chemical reactivities in the atmosphere. The inventory shows total global anthropogenic VOC emissions of about 110,000 Gg/yr, about 10% lower than global VOC inventories developed by other researchers. The study identifies the U.S. as the largest emitter (21% of the total global VOC), followed by the USSR, China, India, and Japan. Globally, fuel wood combustion and savanna burning were among the largest VOC emission sources, accounting for over 35% of the total global VOC emissions. The production and use of gasoline, refuse disposal activities, and organic chemical and rubber manufacturing were also found to be significant sources of global VOC emissions.

  19. Plasma emission sources in analytical spectroscopy-I.

    PubMed

    Greenfield, S; McGeachin, H M; Smith, P B

    1975-01-01

    A critical survey of plasma emission sources used in analytical spectroscopy, excluding conventional arc and spark sources, has been made. In Part I the concept of temperature applied to high-temperature excitation sources is considered, as are arc plasma jets. Part II will be concerned with microwave and capacitively coupled sources and in Part III inductively coupled sources will be dealt with. In the last part a comparison will also be made of all the sources reviewed, from the point of view of sensitivity, precision and freedom from matrix effects.

  20. Aerostat-Lofted Instrument Platform and Sampling Method for Determination of Emissions from Open Area Sources

    EPA Science Inventory

    Sampling emissions from open area sources, particularly sources of open burning, is difficult due to fast dilution of emissions and safety concerns for personnel. Representative emission samples can be difficult to obtain with flaming and explosive sources since personnel safety ...

  1. Aerostat-Lofted Instrument Platform and Sampling Method for Determination of Emissions from Open Area Sources

    EPA Science Inventory

    Sampling emissions from open area sources, particularly sources of open burning, is difficult due to fast dilution of emissions and safety concerns for personnel. Representative emission samples can be difficult to obtain with flaming and explosive sources since personnel safety ...

  2. Classification of nutrient emission sources in the Vistula River system.

    PubMed

    Kowalkowski, Tomasz

    2009-06-01

    Eutrophication of the Baltic sea still remains one of the biggest problems in the north-eastern area of Europe. Recognizing the sources of nutrient emission, classification of their importance and finding the way towards reduction of pollution are the most important tasks for scientists researching this area. This article presents the chemometric approach to the classification of nutrient emission with respect to the regionalisation of emission sources within the Vistula River basin (Poland). Modelled data for mean yearly emission of nitrogen and phosphorus in 1991-2000 has been used for the classification. Seventeen subcatchements in the Vistula basin have been classified according to cluster and factor analyses. The results of this analysis allowed determination of groups of areas with similar pollution characteristics and indicate the need for spatial differentiation of policies and strategies. Three major factors indicating urban, erosion and agricultural sources have been identified as major discriminants of the groups.

  3. Effect of low emission sources on air quality in Cracow

    SciTech Connect

    Nedoma, J.

    1995-12-31

    The paper presents calculation of power engineering low emission and results of stimulation of the effect of this emission on air quality in Cracow, Poland. It has been stated that the segment of low emission in central areas of the town makes up ca. 40% of the observed concentration of sulfur dioxide. Furthermore it has been stated that the capital investment must be concentrated in the central part of the town in order to reach noticeable improvement of air quality in Cracow. Neither the output of a separate power source nor the emission level and its individual harmful effect, but the location of the source and especially packing density of the sources must decide the priority of upgrading actions.

  4. Source Emissions in Multipollutant Air Quality Management

    EPA Science Inventory

    Human activities and natural processes that emit pollutants into the ambient atmosphere are the underlying cause of all air quality problems. In a technical sense, we refer to these activities and processes as pollutant sources. Although air quality management is usually concerne...

  5. Source Emissions in Multipollutant Air Quality Management

    EPA Science Inventory

    Human activities and natural processes that emit pollutants into the ambient atmosphere are the underlying cause of all air quality problems. In a technical sense, we refer to these activities and processes as pollutant sources. Although air quality management is usually concerne...

  6. Comparison of carbon emission and accumulation rates in sub-arctic lakes

    NASA Astrophysics Data System (ADS)

    Lundin, Erik; Bastviken, David; Klaminder, Jonatan; Olid Garcia, Carolina; Karlsson, Jan

    2013-04-01

    Lakes play an important role for the carbon cycling in the sub-arctic landscape by both storing carbon in sediments and by releasing carbon to the atmosphere. Still, our knowledge regarding the importance of carbon accumulation rates vs. carbon emissions in lakes is poor, restricting large scale assessment of source sink potential of lakes in the landscape. In this study we compare annual carbon accumulation rates and CO2 and CH4 emissions to the atmosphere for six Swedish subarctic lakes. We measured the partial pressure of CO2 (every second hour) during the ice free season. CH4 emissions were measured using floating chambers. Furthermore, we sampled sediment cores from each lake (one to three cores per lake depending on lakes sizes) and calculated the recent accumulation rate of carbon into sediments by dating each core, using 210Pb. Total annual carbon emissions (CO2 + CH4) ranged between 5 to 54 g C m-2 yr-1; hence, all lakes were atmospheric net sources of carbon. Carbon emissions were overall dominated by CO2 which made up to over 90 % of the total annual carbon emission in all lakes except one, having low CO2 emission, where CH4 counted for 40% of the annual carbon emission. Sediment carbon accumulation rates were of comparable magnitudes as the emissions, counting for rates of 30 to 60% of the total carbon emission to the atmosphere. This results stress the dual role of subarctic lakes as they are acting both as atmospheric sources of CO2 and CH4 and as significant storages of carbon in sediments.

  7. MICROBIAL VOLATILE ORGANIC COMPOUND EMISSION RATES AND EXPOSURE MODEL

    EPA Science Inventory

    This paper presents the results from a study that examined microbial volatile organic compound (MVOC) emissions from six fungi and one bacterial species (Streptomyces spp.) commonly found in indoor environments. Data are presented on peak emission rates from inoculated agar plate...

  8. MICROBIAL VOLATILE ORGANIC COMPOUND EMISSION RATES AND EXPOSURE MODEL

    EPA Science Inventory

    This paper presents the results from a study that examined microbial volatile organic compound (MVOC) emissions from six fungi and one bacterial species (Streptomyces spp.) commonly found in indoor environments. Data are presented on peak emission rates from inoculated agar plate...

  9. Neptune's non-thermal radio emissions - Phenomenology and source locations

    NASA Technical Reports Server (NTRS)

    Rabl, Gerald K. F.; Ladreiter, H.-P.; Rucker, Helmut O.; Kaiser, Michael L.

    1992-01-01

    During the inbound and the outbound leg of Voyager 2's encounter with Neptune, the Planetary Radio Astronomy (PRA) experiment aboard the spacecraft detected short radio bursts at frequencies within the range of about 500-1300 kHz, and broad-banded smoothly varying emission patterns within the frequency range from about 40-800 kHz. Both emissions can be described in terms of a period of 16.1 hours determining Neptune's rotation period. Furthermore, just near closest approach, a narrow-banded smoothly varying radio component was observed occurring between 600 and 800 kHz. After giving a brief overview about some general characteristics of Neptune's nonthermal radio emission, the source locations of Neptune's emission components are determined, using an offset tilted dipole model for Neptune's magnetic field. Assuming that the emission originates near the electron gyrofrequency a geometrical beaming model is developed in order to fit the observed emission episodes.

  10. WORKSHOP ON SOURCE EMISSION AND AMBIENT AIR MONITORING OF MERCURY

    EPA Science Inventory

    AN EPA/ORD Workshop on Source Emission and Ambient Air Monitoring of Mercury was held on 9/13-14/99, Bloomington, Minnesota. The purpose of the workshop was to discuss the state-of-the-science in source and ambient air mercury monitoring as well as mercury monitoring research and...

  11. 40 CFR Table 1 to Subpart Nnnnnn... - HAP Emissions Sources

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... Sources Process Emissions sources 1. Sodium chromate production a. Ball mill used to grind chromite ore. b. Dryer used to dry chromite ore. c. Rotary kiln used to roast chromite ore to produce sodium chromate. d... system. f. Quench tanks. 2. Sodium dichromate production a. Stack on the electrolytic cell system used to...

  12. 40 CFR Table 1 to Subpart Nnnnnn... - HAP Emissions Sources

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... Sources Process Emissions sources 1. Sodium chromate production a. Ball mill used to grind chromite ore. b. Dryer used to dry chromite ore. c. Rotary kiln used to roast chromite ore to produce sodium chromate. d... system. f. Quench tanks. 2. Sodium dichromate production a. Stack on the electrolytic cell system used to...

  13. 40 CFR 62.08 - Emission inventories and source surveillance.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... surveillance. 62.08 Section 62.08 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... General Provisions § 62.08 Emission inventories and source surveillance. (a) Each subpart identifies the plan provisions for source surveillance which are disapproved, and sets forth the Administrator's...

  14. 40 CFR 62.08 - Emission inventories and source surveillance.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... surveillance. 62.08 Section 62.08 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... General Provisions § 62.08 Emission inventories and source surveillance. (a) Each subpart identifies the plan provisions for source surveillance which are disapproved, and sets forth the Administrator's...

  15. 40 CFR 62.08 - Emission inventories and source surveillance.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... surveillance. 62.08 Section 62.08 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... General Provisions § 62.08 Emission inventories and source surveillance. (a) Each subpart identifies the plan provisions for source surveillance which are disapproved, and sets forth the Administrator's...

  16. 40 CFR 62.08 - Emission inventories and source surveillance.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... surveillance. 62.08 Section 62.08 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... General Provisions § 62.08 Emission inventories and source surveillance. (a) Each subpart identifies the plan provisions for source surveillance which are disapproved, and sets forth the Administrator's...

  17. WORKSHOP ON SOURCE EMISSION AND AMBIENT AIR MONITORING OF MERCURY

    EPA Science Inventory

    AN EPA/ORD Workshop on Source Emission and Ambient Air Monitoring of Mercury was held on 9/13-14/99, Bloomington, Minnesota. The purpose of the workshop was to discuss the state-of-the-science in source and ambient air mercury monitoring as well as mercury monitoring research and...

  18. Locating and quantifying gas emission sources using remotely obtained concentration data

    NASA Astrophysics Data System (ADS)

    Hirst, Bill; Jonathan, Philip; González del Cueto, Fernando; Randell, David; Kosut, Oliver

    2013-08-01

    We describe a method for detecting, locating and quantifying sources of gas emissions to the atmosphere using remotely obtained gas concentration data; the method is applicable to gases of environmental concern. We demonstrate its performance using methane data collected from aircraft. Atmospheric point concentration measurements are modelled as the sum of a spatially and temporally smooth atmospheric background concentration, augmented by concentrations due to local sources. We model source emission rates with a Gaussian mixture model and use a Markov random field to represent the atmospheric background concentration component of the measurements. A Gaussian plume atmospheric eddy dispersion model represents gas dispersion between sources and measurement locations. Initial point estimates of background concentrations and source emission rates are obtained using mixed ℓ2 - ℓ1 optimisation over a discretised grid of potential source locations. Subsequent reversible jump Markov chain Monte Carlo inference provides estimated values and uncertainties for the number, emission rates and locations of sources unconstrained by a grid. Source area, atmospheric background concentrations and other model parameters, including plume model spreading and Lagrangian turbulence time scale, are also estimated. We investigate the performance of the approach first using a synthetic problem, then apply the method to real airborne data from a 1600 km2 area containing two landfills, then a 225 km2 area containing a gas flare stack.

  19. X-Ray Emission from Compact Sources

    SciTech Connect

    Cominsky, L

    2004-03-23

    This paper presents a review of the physical parameters of neutron stars and black holes that have been derived from X-ray observations. I then explain how these physical parameters can be used to learn about the extreme conditions occurring in regions of strong gravity, and present some recent evidence for relativistic effects seen in these systems. A glossary of commonly used terms and a short tutorial on the names of X-ray sources are also included.

  20. Effect of outside air ventilation rate on VOC concentrations and emissions in a call center

    SciTech Connect

    Hodgson, A.T.; Faulkner, D.; Sullivan, D.P.; DiBartolomeo, D.L.; Russell, M.L.; Fisk, W.J.

    2002-01-01

    A study of the relationship between outside air ventilation rate and concentrations of VOCs generated indoors was conducted in a call center. Ventilation rates were manipulated in the building's four air handling units (AHUs). Concentrations of VOCs in the AHU returns were measured on 7 days during a 13-week period. Indoor minus outdoor concentrations and emission factors were calculated. The emission factor data was subjected to principal component analysis to identify groups of co-varying compounds based on source type. One vector represented emissions of solvents from cleaning products. Another vector identified occupant sources. Direct relationships between ventilation rate and concentrations were not observed for most of the abundant VOCs. This result emphasizes the importance of source control measures for limiting VOC concentrations in buildings.

  1. State Budgets, Unit Allocations, and Unit Emissions Rates

    EPA Pesticide Factsheets

    This Technical Support Document (TSD) provides information that supports EPA’s determination of state emissions budgets, unit-level allocations, direct control rate limits, and new unit set-asides for the Transport Rule proposal.

  2. Cumulative carbon emissions, emissions floors and short-term rates of warming: implications for policy.

    PubMed

    Bowerman, Niel H A; Frame, David J; Huntingford, Chris; Lowe, Jason A; Allen, Myles R

    2011-01-13

    A number of recent studies have found a strong link between peak human-induced global warming and cumulative carbon emissions from the start of the industrial revolution, while the link to emissions over shorter periods or in the years 2020 or 2050 is generally weaker. However, cumulative targets appear to conflict with the concept of a 'floor' in emissions caused by sectors such as food production. Here, we show that the introduction of emissions floors does not reduce the importance of cumulative emissions, but may make some warming targets unachievable. For pathways that give a most likely warming up to about 4°C, cumulative emissions from pre-industrial times to year 2200 correlate strongly with most likely resultant peak warming regardless of the shape of emissions floors used, providing a more natural long-term policy horizon than 2050 or 2100. The maximum rate of CO(2)-induced warming, which will affect the feasibility and cost of adapting to climate change, is not determined by cumulative emissions but is tightly aligned with peak rates of emissions. Hence, cumulative carbon emissions to 2200 and peak emission rates could provide a clear and simple framework for CO(2) mitigation policy.

  3. Quantification of Methane Source Locations and Emissions in AN Urban Setting

    NASA Astrophysics Data System (ADS)

    Crosson, E.; Richardson, S.; Tan, S. M.; Whetstone, J.; Bova, T.; Prasad, K. R.; Davis, K. J.; Phillips, N. G.; Turnbull, J. C.; Shepson, P. B.; Cambaliza, M. L.

    2011-12-01

    The regulation of methane emissions from urban sources such as landfills and waste-water treatment facilities is currently a highly debated topic in the US and in Europe. This interest is fueled, in part, by recent measurements indicating that urban emissions are a significant source of Methane (CH4) and in fact may be substantially higher than current inventory estimates(1). As a result, developing methods for locating and quantifying emissions from urban methane sources is of great interest to industries such as landfill and wastewater treatment facility owners, watchdog groups, and the governmental agencies seeking to evaluate or enforce regulations. In an attempt to identify major methane source locations and emissions in Boston, Indianapolis, and the Bay Area, systematic measurements of CH4 concentrations and meteorology data were made at street level using a vehicle mounted cavity ringdown analyzer. A number of discrete sources were detected at concentration levels in excess of 15 times background levels. Using Gaussian plume models as well as tomographic techniques, methane source locations and emission rates will be presented. In addition, flux chamber measurements of discrete sources such as those found in natural gas leaks will also be presented. (1) Wunch, D., P.O. Wennberg, G.C. Toon, G. Keppel-Aleks, and Y.G. Yavin, Emissions of Greenhouse Gases from a North American Megacity, Geophysical Research Letters, Vol. 36, L15810, doi:10.1029/2009GL)39825, 2009.

  4. Miniature field emission light sources for bio-chips

    NASA Astrophysics Data System (ADS)

    Cichy, Bartłomiej; Górecka-Drzazga, Anna; Dziuban, Jan A.

    2009-01-01

    A concept based on preparation of miniature field emission light sources (FELS) for integration with bio-chips is presented. Glass and silicon-glass micro-fluidic systems (biochips) with spectrofluorometric detection are designated for this solution. Planar, miniature silicon-glass field emission light sources were designed and fabricated for this conception. Carbon nanotubes (CNTs) have been used as a low-voltage electron emissive layer. Nanocrystalline yttria matrices doped with rare earth (Re) ions (Re: Eu3+, Tb3+) have been synthesized and utilized as phosphor layers. Light emission spectral characteristics of fabricated sources allow to couple them with typical fluorescent markers as e.g. Alexa, Fluorescein or TO-PRO, used on the wide scale in biochemical researches. Fabricated FELSs are characterized by the intensive and homogenous light emission with well defined sharp emission lines. The efficient and stable field emission from carbon nanotubes has also been noticed. Fabricated FELS are technologically compatible with highly developing micromachined fluidic systems and are able to direct on-chip integration with these microsystems.

  5. Pulsed, atmospheric pressure plasma source for emission spectrometry

    DOEpatents

    Duan, Yixiang; Jin, Zhe; Su, Yongxuan

    2004-05-11

    A low-power, plasma source-based, portable molecular light emission generator/detector employing an atmospheric pressure pulsed-plasma for molecular fragmentation and excitation is described. The average power required for the operation of the plasma is between 0.02 W and 5 W. The features of the optical emission spectra obtained with the pulsed plasma source are significantly different from those obtained with direct current (dc) discharge higher power; for example, strong CH emission at 431.2 nm which is only weakly observed with dc plasma sources was observed, and the intense CN emission observed at 383-388 nm using dc plasma sources was weak in most cases. Strong CN emission was only observed using the present apparatus when compounds containing nitrogen, such as aniline were employed as samples. The present apparatus detects dimethylsulfoxide at 200 ppb using helium as the plasma gas by observing the emission band of the CH radical. When coupled with a gas chromatograph for separating components present in a sample to be analyzed, the present invention provides an apparatus for detecting the arrival of a particular component in the sample at the end of the chromatographic column and the identity thereof.

  6. 40 CFR 63.1505 - Emission standards for affected sources and emission units.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... monitoring option. (f) Sweat furnace. The owner or operator of a sweat furnace shall comply with the emission... operator of a sweat furnace at a secondary aluminum production facility that is a major or area source...

  7. Aircraft-Based Measurements of Point Source Methane Emissions in the Barnett Shale Basin.

    PubMed

    Lavoie, Tegan N; Shepson, Paul B; Cambaliza, Maria O L; Stirm, Brian H; Karion, Anna; Sweeney, Colm; Yacovitch, Tara I; Herndon, Scott C; Lan, Xin; Lyon, David

    2015-07-07

    We report measurements of methane (CH4) emission rates observed at eight different high-emitting point sources in the Barnett Shale, Texas, using aircraft-based methods performed as part of the Barnett Coordinated Campaign. We quantified CH4 emission rates from four gas processing plants, one compressor station, and three landfills during five flights conducted in October 2013. Results are compared to other aircraft- and surface-based measurements of the same facilities, and to estimates based on a national study of gathering and processing facilities emissions and 2013 annual average emissions reported to the U.S. EPA Greenhouse Gas Reporting Program (GHGRP). For the eight sources, CH4 emission measurements from the aircraft-based mass balance approach were a factor of 3.2-5.8 greater than the GHGRP-based estimates. Summed emissions totaled 7022 ± 2000 kg hr(-1), roughly 9% of the entire basin-wide CH4 emissions estimated from regional mass balance flights during the campaign. Emission measurements from five natural gas management facilities were 1.2-4.6 times larger than emissions based on the national study. Results from this study were used to represent "super-emitters" in a newly formulated Barnett Shale Inventory, demonstrating the importance of targeted sampling of "super-emitters" that may be missed by random sampling of a subset of the total.

  8. Control for NOx Emissions from Combustion Sources

    NASA Technical Reports Server (NTRS)

    PozodeFernandez, Maria E.; Collins, Michelle M.

    2000-01-01

    The Environmental Program Office at the Kennedy Space Center is interested in finding solutions and to promote research and development (R&D) that could contribute to solve the problems of air, soil, and groundwater contamination. This study is undertaken as part of NASA's environmental stewardship program. The objective of this study involves the removal of nitrogen oxides from the flue gases of the boilers at KSC using hydrogen peroxide. Phase 1 of this study have shown the potential of this process to be used as an alternative to the current methods of treatment used in the power industry. This report summarizes the research done during the ten-week summer program. During this period, support has been given to implement the modifications suggested for Phase 2 of the project, which focus on oxidation reactions carried at lower temperatures using an ultraviolet source. The redesign and assembly of the modifications for the scrubbing system was the main objective of this research.

  9. Modeling emission rates and exposures from outdoor cooking

    NASA Astrophysics Data System (ADS)

    Edwards, Rufus; Princevac, Marko; Weltman, Robert; Ghasemian, Masoud; Arora, Narendra K.; Bond, Tami

    2017-09-01

    Approximately 3 billion individuals rely on solid fuels for cooking globally. For a large portion of these - an estimated 533 million - cooking is outdoors, where emissions from cookstoves pose a health risk to both cooks and other household and village members. Models that estimate emissions rates from stoves in indoor environments that would meet WHO air quality guidelines (AQG), explicitly don't account for outdoor cooking. The objectives of this paper are to link health based exposure guidelines with emissions from outdoor cookstoves, using a Monte Carlo simulation of cooking times from Haryana India coupled with inverse Gaussian dispersion models. Mean emission rates for outdoor cooking that would result in incremental increases in personal exposure equivalent to the WHO AQG during a 24-h period were 126 ± 13 mg/min for cooking while squatting and 99 ± 10 mg/min while standing. Emission rates modeled for outdoor cooking are substantially higher than emission rates for indoor cooking to meet AQG, because the models estimate impact of emissions on personal exposure concentrations rather than microenvironment concentrations, and because the smoke disperses more readily outdoors compared to indoor environments. As a result, many more stoves including the best performing solid-fuel biomass stoves would meet AQG when cooking outdoors, but may also result in substantial localized neighborhood pollution depending on housing density. Inclusion of the neighborhood impact of pollution should be addressed more formally both in guidelines on emissions rates from stoves that would be protective of health, and also in wider health impact evaluation efforts and burden of disease estimates. Emissions guidelines should better represent the different contexts in which stoves are being used, especially because in these contexts the best performing solid fuel stoves have the potential to provide significant benefits.

  10. Spectra and rates of bremsstrahlung neutrino emission in stars

    NASA Astrophysics Data System (ADS)

    Guo, Gang; Qian, Yong-Zhong

    2016-08-01

    We calculate the energy-differential rate for neutrino emission from electron-nucleus bremsstrahlung in stellar interiors taking into account the effects of electron screening and ionic correlations. We compare the energy-differential and the net rates, as well as the average ν¯e and ν¯x(x =μ ,τ ) energies, for this process with those for e± pair annihilation, plasmon decay, and photoneutrino emission over a wide range of temperature and density. We also compare our updated energy loss rates for the above thermal neutrino emission processes with the fitting formulas widely used in stellar evolution models and determine the temperature and density domain in which each process dominates. We discuss the implications of our results for detection of ν¯e from massive stars during their presupernova evolution and find that pair annihilation makes the predominant contribution to the signal from the thermal emission processes.

  11. Studies of acoustic emission from point and extended sources

    NASA Technical Reports Server (NTRS)

    Sachse, W.; Kim, K. Y.; Chen, C. P.

    1986-01-01

    The use of simulated and controlled acoustic emission signals forms the basis of a powerful tool for the detailed study of various deformation and wave interaction processes in materials. The results of experiments and signal analyses of acoustic emission resulting from point sources such as various types of indentation-produced cracks in brittle materials and the growth of fatigue cracks in 7075-T6 aluminum panels are discussed. Recent work dealing with the modeling and subsequent signal processing of an extended source of emission in a material is reviewed. Results of the forward problem and the inverse problem are presented with the example of a source distributed through the interior of a specimen.

  12. 75 FR 32682 - National Emission Standards for Hazardous Air Pollutants for Major Sources: Industrial...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-06-09

    ... 2050-AG44 National Emission Standards for Hazardous Air Pollutants for Major Sources: Industrial... Pollutants for Area Sources: Industrial, Commercial, and Institutional Boilers; Standards of Performance for New Stationary Sources and Emission Guidelines for Existing Sources: Commercial and Industrial Solid...

  13. Photocathodes for High Repetition Rate Light Sources

    SciTech Connect

    Ben-Zvi, Ilan

    2014-04-20

    This proposal brought together teams at Brookhaven National Laboratory (BNL), Lawrence Berkeley National Laboratory (LBNL) and Stony Brook University (SBU) to study photocathodes for high repetition rate light sources such as Free Electron Lasers (FEL) and Energy Recovery Linacs (ERL). Below details the Principal Investigators and contact information. Each PI submits separately for a budget through his corresponding institute. The work done under this grant comprises a comprehensive program on critical aspects of the production of the electron beams needed for future user facilities. Our program pioneered in situ and in operando diagnostics for alkali antimonide growth. The focus is on development of photocathodes for high repetition rate Free Electron Lasers (FELs) and Energy Recovery Linacs (ERLs), including testing SRF photoguns, both normal-­conducting and superconducting. Teams from BNL, LBNL and Stony Brook University (SBU) led this research, and coordinated their work over a range of topics. The work leveraged a robust infrastructure of existing facilities and the support was used for carrying out the research at these facilities. The program concentrated in three areas: a) Physics and chemistry of alkali-­antimonide cathodes (BNL – LBNL) b) Development and testing of a diamond amplifier for photocathodes (SBU -­ BNL) c) Tests of both cathodes in superconducting RF photoguns (SBU) and copper RF photoguns (LBNL) Our work made extensive use of synchrotron radiation materials science techniques, such as powder-­ and single-­crystal diffraction, x-­ray fluorescence, EXAFS and variable energy XPS. BNL and LBNL have many complementary facilities at the two light sources associated with these laboratories (NSLS and ALS, respectively); use of these will be a major thrust of our program and bring our understanding of these complex materials to a new level. In addition, CHESS at Cornell will be used to continue seamlessly throughout the NSLS dark period and

  14. Discrimination of particulate matter emission sources using stochastic methods

    NASA Astrophysics Data System (ADS)

    Szczurek, Andrzej; Maciejewska, Monika; Wyłomańska, Agnieszka; Sikora, Grzegorz; Balcerek, Michał; Teuerle, Marek

    2016-12-01

    Particulate matter (PM) is one of the criteria pollutants which has been determined as harmful to public health and the environment. For this reason the ability to recognize its emission sources is very important. There are a number of measurement methods which allow to characterize PM in terms of concentration, particles size distribution, and chemical composition. All these information are useful to establish a link between the dust found in the air, its emission sources and influence on human as well as the environment. However, the methods are typically quite sophisticated and not applicable outside laboratories. In this work, we considered PM emission source discrimination method which is based on continuous measurements of PM concentration with a relatively cheap instrument and stochastic analysis of the obtained data. The stochastic analysis is focused on the temporal variation of PM concentration and it involves two steps: (1) recognition of the category of distribution for the data i.e. stable or the domain of attraction of stable distribution and (2) finding best matching distribution out of Gaussian, stable and normal-inverse Gaussian (NIG). We examined six PM emission sources. They were associated with material processing in industrial environment, namely machining and welding aluminum, forged carbon steel and plastic with various tools. As shown by the obtained results, PM emission sources may be distinguished based on statistical distribution of PM concentration variations. Major factor responsible for the differences detectable with our method was the type of material processing and the tool applied. In case different materials were processed by the same tool the distinction of emission sources was difficult. For successful discrimination it was crucial to consider size-segregated mass fraction concentrations. In our opinion the presented approach is very promising. It deserves further study and development.

  15. 2-.mu.m fiber amplified spontaneous emission (ASE) source

    NASA Technical Reports Server (NTRS)

    Jiang, Shibin (Inventor); Wu, Jianfeng (Inventor); Geng, Jihong (Inventor)

    2007-01-01

    A 2-.mu.m fiber Amplified Spontaneous Emission (ASE) source provides a wide emission bandwidth and improved spectral stability/purity for a given output power. The fiber ASE source is formed from a heavy metal oxide multicomponent glass selected from germanate, tellurite and bismuth oxides and doped with high concentrations, 0.5-15 wt. %, thulium oxides (Tm.sub.2O.sub.3) or 0.1-5 wt% holmium oxides (Ho.sub.2O.sub.3) or mixtures thereof. The high concentration of thulium dopants provide highly efficient pump absorption and high quantum efficiency. Co-doping of Tm and Ho can broaden the ASE spectrum.

  16. Independent evaluation of point source fossil fuel CO2 emissions to better than 10.

    PubMed

    Turnbull, Jocelyn Christine; Keller, Elizabeth D; Norris, Margaret W; Wiltshire, Rachael M

    2016-09-13

    Independent estimates of fossil fuel CO2 (CO2ff) emissions are key to ensuring that emission reductions and regulations are effective and provide needed transparency and trust. Point source emissions are a key target because a small number of power plants represent a large portion of total global emissions. Currently, emission rates are known only from self-reported data. Atmospheric observations have the potential to meet the need for independent evaluation, but useful results from this method have been elusive, due to challenges in distinguishing CO2ff emissions from the large and varying CO2 background and in relating atmospheric observations to emission flux rates with high accuracy. Here we use time-integrated observations of the radiocarbon content of CO2 ((14)CO2) to quantify the recently added CO2ff mole fraction at surface sites surrounding a point source. We demonstrate that both fast-growing plant material (grass) and CO2 collected by absorption into sodium hydroxide solution provide excellent time-integrated records of atmospheric (14)CO2 These time-integrated samples allow us to evaluate emissions over a period of days to weeks with only a modest number of measurements. Applying the same time integration in an atmospheric transport model eliminates the need to resolve highly variable short-term turbulence. Together these techniques allow us to independently evaluate point source CO2ff emission rates from atmospheric observations with uncertainties of better than 10%. This uncertainty represents an improvement by a factor of 2 over current bottom-up inventory estimates and previous atmospheric observation estimates and allows reliable independent evaluation of emissions.

  17. Independent evaluation of point source fossil fuel CO2 emissions to better than 10%

    PubMed Central

    Turnbull, Jocelyn Christine; Keller, Elizabeth D.; Norris, Margaret W.; Wiltshire, Rachael M.

    2016-01-01

    Independent estimates of fossil fuel CO2 (CO2ff) emissions are key to ensuring that emission reductions and regulations are effective and provide needed transparency and trust. Point source emissions are a key target because a small number of power plants represent a large portion of total global emissions. Currently, emission rates are known only from self-reported data. Atmospheric observations have the potential to meet the need for independent evaluation, but useful results from this method have been elusive, due to challenges in distinguishing CO2ff emissions from the large and varying CO2 background and in relating atmospheric observations to emission flux rates with high accuracy. Here we use time-integrated observations of the radiocarbon content of CO2 (14CO2) to quantify the recently added CO2ff mole fraction at surface sites surrounding a point source. We demonstrate that both fast-growing plant material (grass) and CO2 collected by absorption into sodium hydroxide solution provide excellent time-integrated records of atmospheric 14CO2. These time-integrated samples allow us to evaluate emissions over a period of days to weeks with only a modest number of measurements. Applying the same time integration in an atmospheric transport model eliminates the need to resolve highly variable short-term turbulence. Together these techniques allow us to independently evaluate point source CO2ff emission rates from atmospheric observations with uncertainties of better than 10%. This uncertainty represents an improvement by a factor of 2 over current bottom-up inventory estimates and previous atmospheric observation estimates and allows reliable independent evaluation of emissions. PMID:27573818

  18. Vacuum cleaner emissions as a source of indoor exposure to airborne particles and bacteria.

    PubMed

    Knibbs, Luke D; He, Congrong; Duchaine, Caroline; Morawska, Lidia

    2012-01-03

    Vacuuming can be a source of indoor exposure to biological and nonbiological aerosols, although there are few data that describe the magnitude of emissions from the vacuum cleaner itself. We therefore sought to quantify emission rates of particles and bacteria from a large group of vacuum cleaners and investigate their potential determinants, including temperature, dust bags, exhaust filters, price, and age. Emissions of particles between 0.009 and 20 μm and bacteria were measured from 21 vacuums. Ultrafine (<100 nm) particle emission rates ranged from 4.0 × 10(6) to 1.1 × 10(11) particles min(-1). Emission of 0.54-20 μm particles ranged from 4.0 × 10(4) to 1.2 × 10(9) particles min(-1). PM(2.5) emissions were between 2.4 × 10(-1) and 5.4 × 10(3) μg min(-1). Bacteria emissions ranged from 0 to 7.4 × 10(5) bacteria min(-1) and were poorly correlated with dust bag bacteria content and particle emissions. Large variability in emission of all parameters was observed across the 21 vacuums, which was largely not attributable to the range of determinant factors we assessed. Vacuum cleaner emissions contribute to indoor exposure to nonbiological and biological aerosols when vacuuming, and this may vary markedly depending on the vacuum used.

  19. Influence of light and temperature on monoterpene emission rates from slash pine

    SciTech Connect

    Tingey, D.T.; Manning, M.; Grothaus, L.C.; Burns, W.F.

    1980-05-01

    There is a growing awareness of vegetation's role as a source of potentially reactive hydrocarbons that may serve as photochemical oxidant precursors. This study assessed the influence of light and temperature, independently, on monoterpene emissions from slash pine (Pinus elliottii Engelm). Plants were preconditioned in0a growth chamber, then transferred to an environmentally controlled gas exchange chamber. Samples of the chamber atmosphere were collected; the monoterpenes were concentrated cryogenically and measured by gas chromatography. Five monoterpenes (..cap alpha..-pinene, ..beta..-pinene, myrcene, limonene, and ..beta..-phellandrene) were present in the vapor phase surrounding the plants in sufficient quantity for reliable measurement. Light did not directly influence monoterpene emission rates since the emissions were similar in both the dark and at various light intensities. Monoterpene emission rates increased exponentially with temperature (i.e. emissions depend on temperature in a log-linear manner). The summed emissions of the five monoterpenes ranged from 3 to 21 micrograms C per grams dry weight per hour as temperature was increased from 20 to 46 C. Initially, emission rates from heat-stressed needles were similar to healthy needles, but rates decreased 11% per day. Daily carbon loss through monoterpene emissions accounted for approximately 0.4% of the carbon fixed during photosynthesis.

  20. Characterization of Methane Emission Sources Using Genetic Algorithms and Atmospheric Transport Modeling

    NASA Astrophysics Data System (ADS)

    Cao, Y.; Cervone, G.; Barkley, Z.; Lauvaux, T.; Deng, A.; Miles, N.; Richardson, S.

    2016-12-01

    Fugitive methane emission rates for the Marcellus shale area are estimated using a genetic algorithm that finds optimal weights to minimize the error between simulated and observed concentrations. The overall goal is to understand the relative contribution of methane due to Shale gas extraction. Methane sensors were installed on four towers located in northeastern Pennsylvania to measure atmospheric concentrations since May 2015. Inverse Lagrangian dispersion model runs are performed from each of these tower locations for each hour of 2015. Simulated methane concentrations at each of the four towers are computed by multiplying the resulting footprints from the atmospheric simulations by thousands of emission sources grouped into 11 classes. The emission sources were identified using GIS techniques, and include conventional and unconventional wells, different types of compressor stations, pipelines, landfills, farming and wetlands. Initial estimates for each source are calculated based on emission factors from EPA and few regional studies. A genetic algorithm is then used to identify optimal emission rates for the 11 classes of methane emissions and to explore extreme events and spatial and temporal structures in the emissions associated with natural gas activities.

  1. Models and statistical methods for gaseous emission testing of finite sources in well-mixed chambers

    NASA Astrophysics Data System (ADS)

    Dunn, James E.

    Two families of mathematical models are proposed to represent either the concentration of a gaseous emission in or the accumulated amount exiting from a well-mixed, environmentally controlled test chamber. A thin film model, which seems applicable to such sources as carpet adhesive, etc., has the capability of isolating the true emission rate constant from chamber effects. It has successfully modeled emissions of methyl ethyl ketone, a C 8 alcohol, and butyl propionate from latex caulk. Chamber effects in the form of temporary wall retention were identified for the latter two compounds. An analogous, deep source, diffusionlimited model for plywood, etc., once fitted to a data set, can be used to generalize to other combinations of source surface area, chamber volume, and air exchange rate.

  2. Industrial source identification and emission estimation of perfluorooctane sulfonate in China.

    PubMed

    Xie, Shuangwei; Wang, Tieyu; Liu, Shijie; Jones, Kevin C; Sweetman, Andrew J; Lu, Yonglong

    2013-02-01

    Perfluorooctane sulfonate (PFOS) and related chemicals (collectively "PFOS equivalents") are currently manufactured and used in a wide variety of industrial processes in China. Since 2003, the national annual production has increased dramatically to accommodate both domestic demands and ongoing overseas needs for metal plating, fire-fighting foams, photographic, semiconductor and aviation industries. Accordingly, PFOS-related industries are significant sources of PFOS to the environment in China, though little information is available. In the present study, industrial sources of PFOS in China were identified and emissions from major related industries, including PFOS manufacture, textile treatment, metal plating, fire-fighting and semiconductor industries, were evaluated. Contribution by various industrial sources and spatial distribution of the PFOS emission were discussed. It was estimated that the total emission of PFOS equivalents in China was 70t in 2010. Industrial use of PFOS in metal plating was identified as the largest source of PFOS pollution at the national level, followed by textile treatment, fire-fighting, PFOS manufacture and semiconductor industry. At the regional level, greater contributions were made by metal plating and textile treatment in most provinces of eastern China, while in the western part of China and several northeastern provinces fire-fighting was the predominant source. The contribution by PFOS manufacture was considerable in Hubei and Fujian provinces. Total emission, emission density and emission intensity showed geographical variations. In general, the eastern coastal provinces, as the most intensively industrialized regions of China, were characterized by significantly higher emission rates, emission density and emission intensity than those in western and northern China. Available monitoring data of PFOS concentrations in surface water of China reflected a similar distribution pattern, confirming that manufacture and industrial

  3. Volatile organic compound concentrations and emission rates in new manufactured and site-built houses.

    PubMed

    Hodgson, A T; Rudd, A F; Beal, D; Chandra, S

    2000-09-01

    Concentrations of 54 volatile organic compounds (VOCs) and ventilation rates were measured in four new manufactured houses over 2-9.5 months following installation and in seven new site-built houses 1-2 months after completion. The houses were in four projects located in hot-humid and mixed-humid climates. They were finished and operational, but unoccupied. Ventilation rates ranged from 0.14-0.78 h-1. Several of the site-built houses had ventilation rates below the ASHRAE recommended value. In both manufactured and site-built houses, the predominant airborne compounds were alpha-pinene, formaldehyde, hexanal, and acetic acid. Formaldehyde concentrations were below or near 50 ppb with a geometric mean value for all houses of 40 ppb. Similarities in the types of VOCs and in VOC concentrations indicated that indoor air quality in the houses was impacted by the same or similar sources. Major identified sources included plywood flooring, latex paint and sheet vinyl flooring. One site-built house was operated at ventilation rates of 0.14 and 0.32 h-1. VOC emission rates calculated at the two conditions agreed within +/- 10% for the most volatile compounds. Generally, the ratios of emission rates at the low and high ventilation rates decreased with decreasing compound volatility. Changes in VOC emission rates in the manufactured houses over 2-9.5 months after installation varied by compound. Only several compounds showed a consistent decrease in emission rate over this period.

  4. Acidic and total primary sulfates: development of emission factors for major stationary combustion sources

    SciTech Connect

    Goklany, I.M.; Hoffnagle, G.F.; Brackbill, E.A.

    1984-01-01

    ''Best estimates'' of emission factors for major sources of acidic and total primary sulfates are developed for use in the compilation of emission inventories for the eastern U.S. These may, in turn, be used for modeling of acidic or sulfate deposition. The factors are based upon a critical evaluation of the generic measurement methods used to quantify total and acidic primary sulfate emissions, and an exhaustive review and critique of individual papers and studies available in the open literature which present measurement data on primary sulfate emissions. It develops a qualitative rating scheme which specifies the level of confidence that should be attached to the emission factor determinations. The paper concludes that much of the existing data on primary sulfates from stationary combustion sources are, probably, significantly biased upward and, therefore, inappropriate for the derivation of emission factors. Therefore, existing estimates of primary sulfate emissions for these source categories are, probably, substanitally inflated. It also concludes that, for most source categories, very little confidence can be attached to the best estimates because of the paucity of data obtained from measurement techniques which are likely to be free of systematic bias. 68 references.

  5. Identification of surface NOx emission sources on a regional scale using OMI NO2

    NASA Astrophysics Data System (ADS)

    Zyrichidou, I.; Κoukouli, M. E.; Balis, D.; Markakis, K.; Poupkou, A.; Katragkou, E.; Kioutsioukis, I.; Melas, D.; Boersma, K. F.; van Roozendael, M.

    2015-01-01

    In this study, an inverse modeling technique is applied to obtain, at a regional scale, top-down emission estimates for nitrogen oxides utilizing tropospheric nitrogen dioxide (NO2) columns retrieved by the OMI/Aura instrument and estimated by the Comprehensive Air Quality Model with extensions (CAMx). The main idea, applied previously using models with coarse spatial resolution, is to combine the a priori information from the bottom up emission inventory used in an air quality simulation that covers the Balkan peninsula in a high resolution grid (0.1° × 0.1°) with the tropospheric NO2 quantities estimated for one complete year by CAMx and the tropospheric NO2 columns retrieved by satellite observations in order to identify missing emissions sources on a regional scale. The results have identified biases between the a priori and a posteriori emission inventories due to the missing emission sources or over-estimation of the spread and quantity of certain emission sources. In such a fine resolution grid we have also analyzed and considered the horizontal transport on the a posteriori NOx emissions. The deduced a posteriori NOx emissions, dominated by the fossil fuel emissions, were found to be1.11 ± 0.30 Tg N/y, compared to 0.87 ± 0.43 Tg N/y found in the a priori Balkan emission inventory. Soil emissions over the extended Greek domain, omitted in the a priori inventory, were estimated to account for almost 20% of the total emitted amount, while for the year 2009 the biomass burning NOx emission flux was also estimated and the average rate accounted for 0.5 × 10-6 Tg N/km2.

  6. Radio emission from an ultraluminous x-ray source.

    PubMed

    Kaaret, Philip; Corbel, Stephane; Prestwich, Andrea H; Zezas, Andreas

    2003-01-17

    The physical nature of ultraluminous x-ray sources is uncertain. Stellar-mass black holes with beamed radiation and intermediate black holes with isotropic radiation are two plausible explanations. We discovered radio emission from an ultraluminous x-ray source in the dwarf irregular galaxy NGC 5408. The x-ray, radio, and optical fluxes as well as the x-ray spectral shape are consistent with beamed relativistic jet emission from an accreting stellar black hole. If confirmed, this would suggest that the ultraluminous x-ray sources may be stellar-mass rather than intermediate-mass black holes. However, interpretation of the source as a jet-producing intermediate-mass black hole cannot be ruled out at this time.

  7. TRANSIT BUS LOAD-BASED MODAL EMISSION RATE MODEL DEVELOPMENT

    EPA Science Inventory

    Heavy-duty diesel vehicles (HDDVs) operations are a major source of oxides of nitrogen (NOx) and particulate matter (PM) emissions in metropolitan area nationwide. Although HD¬DVs constitute a small portion of the on-road fleet, they typically contribute more than 45% of NOx and ...

  8. 40 CFR 74.22 - Actual SO2 emissions rate.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ....6 for natural gas For other fuels, the combustion source must specify the SO2 emissions factor. (c... thousand barrels for oil and pounds per million cubic feet (scf) for gas, shall be calculated as follows... this section; “control system efficiency” is as defined under § 60.48(a) and part 60, appendix A...

  9. 40 CFR 74.22 - Actual SO2 emissions rate.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ....6 for natural gas For other fuels, the combustion source must specify the SO2 emissions factor. (c... thousand barrels for oil and pounds per million cubic feet (scf) for gas, shall be calculated as follows... this section; “control system efficiency” is as defined under § 60.48(a) and part 60, appendix A...

  10. TRANSIT BUS LOAD-BASED MODAL EMISSION RATE MODEL DEVELOPMENT

    EPA Science Inventory

    Heavy-duty diesel vehicles (HDDVs) operations are a major source of oxides of nitrogen (NOx) and particulate matter (PM) emissions in metropolitan area nationwide. Although HD¬DVs constitute a small portion of the on-road fleet, they typically contribute more than 45% of NOx and ...

  11. Source Attribution of Methane Emissions in Northeastern Colorado Using Ammonia to Methane Emission Ratios

    NASA Astrophysics Data System (ADS)

    Eilerman, S. J.; Neuman, J. A.; Peischl, J.; Aikin, K. C.; Ryerson, T. B.; Perring, A. E.; Robinson, E. S.; Holloway, M.; Trainer, M.

    2015-12-01

    Due to recent advances in extraction technology, oil and natural gas extraction and processing in the Denver-Julesburg basin has increased substantially in the past decade. Northeastern Colorado is also home to over 250 concentrated animal feeding operations (CAFOs), capable of hosting over 2 million head of ruminant livestock (cattle and sheep). Because of methane's high Global Warming Potential, quantification and attribution of methane emissions from oil and gas development and agricultural activity are important for guiding greenhouse gas emission policy. However, due to the co-location of these different sources, top-down measurements of methane are often unable to attribute emissions to a specific source or sector. In this work, we evaluate the ammonia:methane emission ratio directly downwind of CAFOs using a mobile laboratory. Several CAFOs were chosen for periodic study over a 12-month period to identify diurnal and seasonal variation in the emission ratio as well as differences due to livestock type. Using this knowledge of the agricultural ammonia:methane emission ratio, aircraft measurements of ammonia and methane over oil and gas basins in the western US during the Shale Oil and Natural Gas Nexus (SONGNEX) field campaign in March and April 2015 can be used for source attribution of methane emissions.

  12. Mapping methane emission sources over California based on airborne measurements

    NASA Astrophysics Data System (ADS)

    Karl, T.; Guha, A.; Peischl, J.; Misztal, P. K.; Jonsson, H.; Goldstein, A. H.; Ryerson, T. B.

    2011-12-01

    The California Global Warming Solutions Act of 2006 (AB 32) has created a need to accurately characterize the emission sources of various greenhouse gases (GHGs) and verify the existing state GHG inventory. Methane (CH4) is a major GHG with a global warming potential of 20 times that of CO2 and currently constitutes about 6% of the total statewide GHG emissions on a CO2 equivalent basis. Some of the major methane sources in the state are area sources where methane is biologically produced (e.g. dairies, landfills and waste treatment plants) making bottom-up estimation of emissions a complex process. Other potential sources include fugitive emissions from oil extraction processes and natural gas distribution network, emissions from which are not well-quantified. The lack of adequate field measurement data to verify the inventory and provide independently generated estimates further contributes to the overall uncertainty in the CH4 inventory. In order to gain a better perspective of spatial distribution of major CH4 sources in California, a real-time measurement instrument based on Cavity Ring Down Spectroscopy (CRDS) was installed in a Twin Otter aircraft for the CABERNET (California Airborne BVOC Emissions Research in Natural Ecosystems Transects) campaign, where the driving research goal was to understand the spatial distribution of biogenic VOC emissions. The campaign took place in June 2011 and encompassed over forty hours of airborne CH4 and CO2 measurements during eight unique flights which covered much of the Central Valley and its eastern edge, the Sacramento-San Joaquin delta and the coastal range. The coincident VOC measurements, obtained through a high frequency proton transfer reaction mass spectrometer (PTRMS), aid in CH4 source identification. High mixing ratios of CH4 (> 2000 ppb) are observed consistently in all the flight transects above the Central Valley. These high levels of CH4 are accompanied by high levels of methanol which is an important

  13. 40 CFR 62.08 - Emission inventories and source surveillance.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... surveillance. 62.08 Section 62.08 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) APPROVAL AND PROMULGATION OF STATE PLANS FOR DESIGNATED FACILITIES AND POLLUTANTS General Provisions § 62.08 Emission inventories and source surveillance. (a) Each subpart identifies the...

  14. REVIEW OF INDOOR EMISSION SOURCE MODELS: PART 2. PARAMETER ESTIMATION

    EPA Science Inventory

    This review consists of two sections. Part I provides an overview of 46 indoor emission source models. Part 2 (this paper) focuses on parameter estimation, a topic that is critical to modelers but has never been systematically discussed. A perfectly valid model may not be a usefu...

  15. Identification of emission sources of umbral flashes using phase congruency

    NASA Astrophysics Data System (ADS)

    Feng, Song; Yu, Lan; Yang, Yun-Fei; Ji, Kai-Fan

    2014-08-01

    The emission sources of umbral flashes (UFs) are believed to be closely related to running umbral and penumbral waves, and are concluded to be associated with umbral dots in the solar photosphere. Accurate identification of emission sources of UFs is crucial for investigating these physical phenomena and their inherent relationships. A relatively novel model of shape perception, namely phase congruency (PC), uses phase information in the Fourier domain to identify the geometrical shape of the region of interest in different intensity levels, rather than intensity or gradient. Previous studies indicate that the model is suitable for identifying features with low contrast and low luminance. In the present paper, we applied the PC model to identify the emission sources of UFs and to locate their positions. For illustrating the high performance of our proposed method, two time sequences of Ca II H images derived from the Hinode/SOT on 2010 August 10 and 2013 August 20 were used. Furthermore, we also compared these results with the analysis results that are identified by the traditional/classical identification methods, including the gray-scale adjusted technique and the running difference technique. The result of our analysis demonstrates that our proposed method is more accurate and effective than the traditional identification methods when applied to identifying the emission sources of UFs and to locating their positions.

  16. 40 CFR 60.25 - Emission inventories, source surveillance, reports.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... previous progress reports. (6) Submission of copies of technical reports on all performance testing on... surveillance, reports. 60.25 Section 60.25 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... State Plans for Designated Facilities § 60.25 Emission inventories, source surveillance, reports....

  17. 40 CFR 60.25 - Emission inventories, source surveillance, reports.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... previous progress reports. (6) Submission of copies of technical reports on all performance testing on... surveillance, reports. 60.25 Section 60.25 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... State Plans for Designated Facilities § 60.25 Emission inventories, source surveillance, reports....

  18. 40 CFR 60.25 - Emission inventories, source surveillance, reports.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... previous progress reports. (6) Submission of copies of technical reports on all performance testing on... surveillance, reports. 60.25 Section 60.25 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... State Plans for Designated Facilities § 60.25 Emission inventories, source surveillance, reports....

  19. 40 CFR 60.25 - Emission inventories, source surveillance, reports.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... previous progress reports. (6) Submission of copies of technical reports on all performance testing on... surveillance, reports. 60.25 Section 60.25 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... State Plans for Designated Facilities § 60.25 Emission inventories, source surveillance, reports....

  20. 40 CFR 60.25 - Emission inventories, source surveillance, reports.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... previous progress reports. (6) Submission of copies of technical reports on all performance testing on... surveillance, reports. 60.25 Section 60.25 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... State Plans for Designated Facilities § 60.25 Emission inventories, source surveillance, reports....

  1. Emission rates of organics from vegetation in California's Central Valley

    NASA Astrophysics Data System (ADS)

    Winer, Arthur M.; Arey, Janet; Atkinson, Roger; Aschmann, Sara M.; Long, William D.; Morrison, C. Lynn; Olszyk, David M.

    Rates of emission of speciated hydrocarbons have been determined for more than 30 of the most dominant (based on acreage) agricultural and natural plant types found in California's Central Valley. These measurements employed flow-through Teflon chambers, sample collection on solid adsorbent and thermal desorption gas chromatography (GC) and GC-mass spectrometry analysis to identify more than 40 individual organic compounds. In addition to isoprene and the monoterpenes, we observed sesquiterpenes, alcohols, acetates, aldehydes, ketones, ethers, esters, alkanes, alkenes and aromatics as emissions from these plant species. Mean emission rates for total monoterpenes ranged from none detected in the case of beans, grapes, rice and wheat, to as high as 12-30 μg h -1 g -1 for pistachio and tomato (normalized to dry leaf and total biomass, respectively). Other agricultural species exhibiting substantial rates of emission of monoterpenes included carrot, cotton, lemon, orange and walnut. All of the plant species studied showed total assigned compound emission rates in the range between 0.1 and 36 νg h -1 g -1.

  2. Monoterpene emission rate measurements from a Monterey pine

    SciTech Connect

    Juuti, S. ); Arey, J.; Atkinson, R. )

    1990-05-20

    The monoterpenes emitted from a Monterey pine (pinus radiata) were investigated using a dynamic flow-through enclosure technique. The monoterpenes identified and quantified were {alpha}- and {beta}-pinene, d-limonene + {beta} phellandrene, myrcene, camphene and {Delta}{sup 3}-carene, with {alpha}- and {beta}-pinene accounting for over 80% of the total monoterpene emissions. The monoterpene emission rate increased with temperature, in good agreement with previous data for other coniferous species. The absence of added CO{sub 2} to the synthetic air flow stream, exposure to elevated levels (300-500 ppb mixing ratio) of O{sub 3} for 3-4 hours, and increased air movement within the enclosure, had no observable effect on the monoterpene emission rate at a given temperature. In contrast, rough handling of the pine during the sampling protocol resulted in increases in the monoterpene emission rate by factors of 10-50. These results will be useful to those designing enclosure sampling protocols for the determination of the emission rates of biogenic organic compounds from vegetation.

  3. TEST METHODS TO CHARACTERIZE PARTICULATE MATTER EMISSIONS AND DEPOSITION RATES IN A RESEARCH HOUSE

    EPA Science Inventory

    The paper discusses test methods to characterize particulate matter (PM) emissions and deposition rates in a research house. In a room in the research house, specially configured for PM source testing, a high-efficiency particulate air (HEPA)-filtered air supply system, used for...

  4. TEST METHODS TO CHARACTERIZE PARTICULATE MATTER EMISSIONS AND DEPOSITION RATES IN A RESEARCH HOUSE

    EPA Science Inventory

    The paper discusses test methods to characterize particulate matter (PM) emissions and deposition rates in a research house. In a room in the research house, specially configured for PM source testing, a high-efficiency particulate air (HEPA)-filtered air supply system, used for...

  5. 40 CFR Appendix C to Part 60 - Determination of Emission Rate Change

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 7 2011-07-01 2011-07-01 false Determination of Emission Rate Change C Appendix C to Part 60 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES (CONTINUED) Pt. 60, App. C Appendix C to Part...

  6. VUV Emission of Microwave Driven Argon Plasma Source

    NASA Astrophysics Data System (ADS)

    Henriques, Julio; Espinho, Susana; Felizardo, Edgar; Tatarova, Elena; Dias, Francisco; Ferreira, Carlos

    2013-09-01

    An experimental and kinetic modeling investigation of a low-pressure (0.1-1.2 mbar), surface wave (2.45 GHz) induced Ar plasma as a source vacuum ultraviolet (VUV) light is presented, using visible and VUV optical spectroscopy. The electron density and the relative VUV emission intensities of excited Ar atoms (at 104.8 nm and 106.6 nm) and ions (at 92.0 nm and 93.2 nm) were determined as a function of the microwave power and pressure. The experimental results were analyzed using a 2D self-consistent theoretical model based on a set of coupled equations including the electron Boltzmann equation, the rate balance equations for the most important electronic excited species and for charged particles, the gas thermal balance equation, and the wave electrodynamics. The principal collisional and radiative processes for neutral Ar(3p54s) and Ar(3p54p) and ionized Ar(3s3p6 2S1/2) levels are accounted for. Model predictions are in good agreement with the experimental measurements. This study was funded by the Foundation for Science and Technology, Portuguese Ministry of Education and Science, under the research contract PTDC/FIS/108411/2008.

  7. Characterization of gaseous pollutant and particulate matter emission rates from a commercial broiler operation part II: Correlated emission rates

    NASA Astrophysics Data System (ADS)

    Roumeliotis, Taylor S.; Dixon, Brad J.; Van Heyst, Bill J.

    2010-10-01

    Emission rates of ammonia, acid gases, inorganic aerosols, methane, and size fractionated particulate matter were measured from a commercial broiler facility. This paper discusses the statistically influential parameters on numerous pollutants' emission from a broiler chicken facility and generates emission correlations to fill data gaps and develop averaged emission factors. Live mass of the birds was commonly a significant variable to each pollutant's emission. Some variables significantly impacted the pollutants' emissions, such as litter moisture content, but were measured discretely and cannot be used for filling in data gaps. House parameter correlations were, therefore, developed using parameters measured at the facility, such as indoor temperature, relative humidity, and the live mass of the birds, and relied on the mutual behaviour of discretely measured explanatory parameters and continuously monitored confounding variables. The live mass and the difference in the indoor temperature and the house set-point temperature were the most significant variables in each pollutant's correlation. The correlations predicted each pollutants emission to within 20% (total mass basis) over most broiler production cycles. Their validation on independent datasets also successfully estimated the flocks' emissions to within 3%. Emission factors (EFs) were developed for methane, ammonia, and size fractionated particulate matter using measured data and correlated emissions to fill in data gaps. PM 10 (particulate matter ≤10 microns) EFs were estimated to be 4.6 and 5.9 g d -1 [Animal Unit, AU] -1 for five and six week production cycles, respectively. PM 2.5 (PM ≤ 2.5 microns) EFs were 0.8 and 1.4 g d -1 AU -1 for five and six week cycles, respectively. Ammonia and methane emission factors were estimated at 120.8 and 197.0 g d -1 AU -1, respectively for a five week production cycle.

  8. Airborne reduced nitrogen: ammonia emissions from agriculture and other sources.

    PubMed

    Anderson, Natalie; Strader, Ross; Davidson, Cliff

    2003-06-01

    Ammonia is a basic gas and one of the most abundant nitrogen-containing compounds in the atmosphere. When emitted, ammonia reacts with oxides of nitrogen and sulfur to form particles, typically in the fine particle size range. Roughly half of the PM(2.5) mass in eastern United States is ammonium sulfate, according to the US EPA. Results from recent studies of PM(2.5) show that these fine particles are typically deposited deep in the lungs and may lead to increased morbidity and/or mortality. Also, these particles are in the size range that will degrade visibility. Ammonia emission inventories are usually constructed by multiplying an activity level by an experimentally determined emission factor for each source category. Typical sources of ammonia include livestock, fertilizer, soils, forest fires and slash burning, industry, vehicles, the oceans, humans, pets, wild animals, and waste disposal and recycling activities. Livestock is the largest source category in the United States, with waste from livestock responsible for about 3x10(9) kg of ammonia in 1995. Volatilization of ammonia from livestock waste is dependent on many parameters, and thus emission factors are difficult to predict. Despite a seasonal variation in these values, the emission factors for general livestock categories are usually annually averaged in current inventories. Activity levels for livestock are from the USDA Census of Agriculture, which does not give information about animal raising practices such as housing types and grazing times, waste handling systems, and approximate animal slurry spreading times or methods. Ammonia emissions in the United States in 1995 from sources other than livestock are much lower; for example, annual emissions are roughly 8x10(8) kg from fertilizer, 7x10(7) kg from industry, 5x10(7) kg from vehicles and 1x10(8) kg from humans. There is considerable uncertainty in the emissions from soil and vegetation, although this category may also be significant

  9. ALMA Band 8 Continuum Emission from Orion Source I

    NASA Astrophysics Data System (ADS)

    Hirota, Tomoya; Machida, Masahiro N.; Matsushita, Yuko; Motogi, Kazuhito; Matsumoto, Naoko; Kim, Mi Kyoung; Burns, Ross A.; Honma, Mareki

    2016-12-01

    We have measured continuum flux densities of a high-mass protostar candidate, a radio source I in the Orion KL region (Orion Source I) using the Atacama Large Millimeter/Submillimeter Array (ALMA) at band 8 with an angular resolution of 0.″1. The continuum emission at 430, 460, and 490 GHz associated with Source I shows an elongated structure along the northwest-southeast direction perpendicular to the so-called low-velocity bipolar outflow. The deconvolved size of the continuum source, 90 au × 20 au, is consistent with those reported previously at other millimeter/submillimeter wavelengths. The flux density can be well fitted to the optically thick blackbody spectral energy distribution, and the brightness temperature is evaluated to be 700-800 K. It is much lower than that in the case of proton-electron or H- free-free radiations. Our data are consistent with the latest ALMA results by Plambeck & Wright, in which the continuum emission was proposed to arise from the edge-on circumstellar disk via thermal dust emission, unless the continuum source consists of an unresolved structure with a smaller beam filling factor.

  10. Source characteristics of Jovian narrow-band kilometric radio emissions

    NASA Astrophysics Data System (ADS)

    Reiner, M. J.; Fainberg, J.; Stone, R. G.; Kaiser, M. L.; Desch, M. D.; Manning, R.; Zarka, P.; Pedersen, B.-M.

    1993-07-01

    New observations of Jovian narrow-band kilometric (nKOM) radio emissions were made by the Unified Radio and Plasma Wave (URAP) experiment on the Ulysses spacecraft during the Ulysses-Jupiter encounter in early February 1992. These observations have demonstrated the unique capability of the URAP instrument for determining both the direction and polarization of nKOM radio sources. An important result is the discovery that nKOM radio emission originates from a number of distinct sources located at different Jovian longitudes and at the inner and outermost regions of the Io plasma torus. These sources have been tracked for several Jovian rotations, yielding their corotational lags, their spatial and temporal evolution, and their radiation characteristics at both low latitudes far from Jupiter and at high latitudes near the planet. Both right-hand and left-hand circularly polarized nKOM sources were observed. The polarizations observed for sources in the outermost regions of the torus seem to favor extraordinary mode emission.

  11. Particulate matter composition and emission rates from the disk incorporation of class B biosolids into soil

    NASA Astrophysics Data System (ADS)

    Paez-Rubio, Tania; Xin, Hua; Anderson, James; Peccia, Jordan

    Biosolids contain metal, synthetic organic compound, endotoxin, and pathogen concentrations that are greater than concentrations in the agricultural soils to which they are applied. Once applied, biosolids are incorporated into soils by disking and the aerosols produced during this process may pose an airborne toxicological and infectious health hazard to biosolids workers and nearby residents. Field studies at a Central Arizona biosolids land application site were conducted to characterize the physical, chemical, and biological content of the aerosols produced during biosolids disking and the content of bulk biosolids and soils from which the aerosols emanate. Arrayed samplers were used to estimate the vertical source aerosol concentration profile to enable plume height and associated source emission rate calculations. Source aerosol concentrations and calculated emission rates reveal that disking is a substantial source of biosolids-derived aerosols. The biosolids emission rate during disking ranged from 9.91 to 27.25 mg s -1 and was greater than previously measured emission rates produced during the spreading of dewatered biosolids or the spraying of liquid biosolids. Adding biosolids to dry soils increased the moisture content and reduced the total PM 10 emissions produced during disking by at least three times. The combination of bulk biosolids and aerosol measurements along with PM 10 concentrations provides a framework for estimating aerosol concentrations and emission rates by reconstruction. This framework serves to eliminate the difficulty and inherent limitations associated with monitoring low aerosol concentrations of toxic compounds and pathogens, and can promote an increased understanding of the associated biosolids aerosol health risks to workers and nearby residents.

  12. Rep-rate explosive whisker emission cathode investigations

    NASA Astrophysics Data System (ADS)

    Litz, Marc S.; Golden, Jeffry

    1994-05-01

    An experiment is underway to study the performance of several materials as field-emission cathodes for low voltage (rate. This provides a high average power (50 kW) test bed for the study. A comparison is made of cathodes fabricated from velvet, carbon, diamond coatings, niobium wire nanocomposite, and poly-crystalline tungsten. Surface emission is monitored by an array of Faraday cups. The `turn-on' time, uniformity of emission, and gap closure time are measured as a function of the spatially averaged, macroscopic electric field at the cathode. The carbon fiber cathode produces the largest current density and has the lowest threshold voltage for emission.

  13. EPA's mobile monitoring of source emissions and near-source impact

    EPA Science Inventory

    Real-time ambient monitoring onboard a moving vehicle is a unique data collection approach applied to characterize large-area sources, such as major roadways, and detect fugitive emissions from distributed sources, such as leaking oil wells. EPA's Office of Research and Developme...

  14. EPA's mobile monitoring of source emissions and near-source impact

    EPA Science Inventory

    Real-time ambient monitoring onboard a moving vehicle is a unique data collection approach applied to characterize large-area sources, such as major roadways, and detect fugitive emissions from distributed sources, such as leaking oil wells. EPA's Office of Research and Developme...

  15. Source dynamics of the microwave emission during a solar flare

    NASA Astrophysics Data System (ADS)

    Begum Shaik, Shaheda; Gary, Dale E.; Nita, Gelu M.

    2016-05-01

    Determining the microwave burst source characteristics is important to understand the parameters of the flare process which produce the microwave emission. Previous studies show that the microwave solar bursts do typically exhibit a single source of emission but also often show inhomogeneous sources as a function of frequency at some periods during the burst. This study focuses on the spectral and spatial dynamics of the microwave gyrosynchrotron source through the microwave spectral and imaging analysis. We report the source characteristics of few impulsive flare events observed by the newly upgraded Expanded Owens Valley Solar Array (EOVSA) in the frequency range of 2.5 to 18 GHz and from the complimentary data of (Nobeyama Radioheliograph / Nobeyama Radio Polarimeters) NoRH / NoRP. The low frequency optically thick part of the microwave spectrum is an indicator of spatial inhomogeneity and complexity of the sources. We concentrate in the dynamics of the low frequency spectrum (intensity and spectral index) measured by EOVSA, and compare it to the corresponding spatial propoerties of the NoRH sources observed at 17 GHz and to the loop structures seen in the EUV (Extreme Ultraviolet) images with SDO (Solar Dynamics Observatory).

  16. EPA`s emissions models for general nonroad sources

    SciTech Connect

    Fieber, J.; Rosenbaum, A.; Vranka, R.; Kleinhesselink, D.

    1996-12-31

    Under the sponsorship of the US EPA`s Office of Mobile Sources, SAI has developed a computer model for nonroad mobile sources. Although data and methodologies continue to be revisited, the alpha version of the model has been completed and is currently under review at EPA. The model contains modules for estimating equipment populations, activity, emission factors, and total emissions. It adjusts these estimates to predict total emissions for the calendar year and at a level of detail specified by the user (e.g., average annual estimates at a national level, hourly estimates for a specific county). The EPA`s nonroad model provides estimates for the following general classes of nonroad equipment: General Nonroad Sources: (1) Lawn and garden equipment; (2) Airport service equipment; (3) Recreational; (4) Light Commercial; (5) Industrial; (6) Construction; (7) Agricultural; and (8) Logging. Special Nonroad Sources: (1) Locomotives; (2) Aircraft; and (3) Marine Vessels. With the exception of locomotives, aircraft, and marine vessels, the methodologies used within the model are quite similar for all these source groupings. Information for specific equipment types (e.g., 15-25 horsepower, gasoline 2-stroke engine commercial turf equipment) will also be provided if the user requests this level of detail. Written in FORTRAN and designed for personal computers (though it can be ported to workstations), this new emissions tool includes an interface to improve its ease of use and flexibility. We present here some of the features of the model and provide an overview of the internal methods used for the equipment groups listed under general nonroad sources.

  17. Study Pinpoints Sources of Polluting Vehicle Emissions (Fact Sheet)

    SciTech Connect

    Not Available

    2012-03-01

    aftertreatment, high-molecular-weight fuel components and unburned lubricant were emitted at higher rates than in vehicles in good repair, with functioning emissions systems. Light-duty gasoline, medium-duty diesel, and heavy-duty natural gas vehicles produced more particles with fresh oil than with aged oil. The opposite trend was observed in light- and medium-duty high PM emitters. This effect was not readily apparent with heavy-duty diesel vehicles, perhaps because the lubricant represented a much smaller fraction of the total PM in those trucks.

  18. HVAC SYSTEMS AS EMISSION SOURCES AFFECTING INDOOR AIR QUALITY: A CRITICAL REVIEW

    EPA Science Inventory

    The study evaluates heating, ventilating, and air-conditioning (HVAC) systems as contaminant emission sources that affect indoor air quality (IAQ). Various literature sources and methods for characterizing HVAC emission sources are reviewed. Available methods include in situ test...

  19. HVAC SYSTEMS AS EMISSION SOURCES AFFECTING INDOOR AIR QUALITY: A CRITICAL REVIEW

    EPA Science Inventory

    The study evaluates heating, ventilating, and air-conditioning (HVAC) systems as contaminant emission sources that affect indoor air quality (IAQ). Various literature sources and methods for characterizing HVAC emission sources are reviewed. Available methods include in situ test...

  20. A simple method for screening emission sources of carbonyl compounds in indoor air.

    PubMed

    Yamashita, Shohei; Kume, Kazunari; Horiike, Toshiyuki; Honma, Nobuyuki; Fusaya, Masahiro; Ohura, Takeshi; Amagai, Takashi

    2010-06-15

    Volatile organic compounds (VOCs) emitted from building and furnishing materials are frequently observed in high concentrations in indoor air. Nondestructive analytical methods that determine the main parameters influencing concentration of the chemical substances are necessary to screen for sources of VOC emissions. Toward this goal, we have developed a new flux sampler, referred to herein as an emission cell for simultaneous multi-sampling (ECSMS), that is used for screening indoor emission sources of VOCs and for determining the emission rates of these sources. Because the ECSMS is based on passive sampling, it can be easily used on-site at a low cost. Among VOCs, low-molecular-weight carbonyl compounds including formaldehyde are frequently detected at high concentrations in indoor environments. In this study, we determined the reliability of the ECSMS for the collection of formaldehyde and other carbonyl compounds emitted from wood-based composites of medium density fiberboards and particleboards. We then used emission rates determined by the ECSMS to predict airborne concentrations of formaldehyde emitted from a bookshelf in a large chamber, and these data were compared to formaldehyde concentrations that were acquired simultaneously by means of an active sampling method. The values obtained from the two methods were quite similar, suggesting that ECSMS measurement is an effective method for screening primary sources influencing indoor concentrations of formaldehyde. Copyright 2010 Elsevier B.V. All rights reserved.

  1. Large spontaneous emission rate enhancement in grating coupled hyperbolic metamaterials.

    PubMed

    Sreekanth, Kandammathe Valiyaveedu; Krishna, Koduru Hari; De Luca, Antonio; Strangi, Giuseppe

    2014-09-11

    Hyperbolic metamaterial (HMM), a sub-wavelength periodic artificial structure with hyperbolic dispersion, can enhance the spontaneous emission of quantum emitters. Here, we demonstrate the large spontaneous emission rate enhancement of an organic dye placed in a grating coupled hyperbolic metamaterial (GCHMM). A two-dimensional (2D) silver diffraction grating coupled with an Ag/Al2O3 HMM shows 18-fold spontaneous emission decay rate enhancement of dye molecules with respect to the same HMM without grating. The experimental results are compared with analytical models and numerical simulations, which confirm that the observed enhancement of GCHMM is due to the outcoupling of non-radiative plasmonic modes as well as strong plasmon-exciton coupling in HMM via diffracting grating.

  2. Bacterial aerosol emission rates from municipal wastewater aeration tanks.

    PubMed Central

    Sawyer, B; Elenbogen, G; Rao, K C; O'Brien, P; Zenz, D R; Lue-Hing, C

    1993-01-01

    In this report we describe the results of a study conducted to determine the rates of bacterial aerosol emission from the surfaces of the aeration tanks of the Metropolitan Water Reclamation District of Greater Chicago John E. Egan Water Reclamation Plant. This study was accomplished by conducting test runs in which Andersen six-stage viable samplers were used to collect bacterial aerosol samples inside a walled tower positioned above an aeration tank liquid surface at the John E. Egan Water Reclamation Plant. The samples were analyzed for standard plate counts (SPC), total coliforms (TC), fecal coliforms, and fecal streptococci. Two methods of calculation were used to estimate the bacterial emission rate. The first method was a conventional stack emission rate calculation method in which the measured air concentration of bacteria was multiplied by the air flow rate emanating from the aeration tanks. The second method was a more empirical method in which an attempt was made to measure all of the bacteria emanating from an isolated area (0.37 m2) of the aeration tank surface over time. The data from six test runs were used to determine bacterial emission rates by both calculation methods. As determined by the conventional calculation method, the average SPC emission rate was 1.61 SPC/m2/s (range, 0.66 to 2.65 SPC/m2/s). As determined by the empirical calculation method, the average SPC emission rate was 2.18 SPC/m2/s (range, 1.25 to 2.66 SPC/m2/s). For TC, the average emission rate was 0.20 TC/m2/s (range, 0.02 to 0.40 TC/m2/s) when the conventional calculation method was used and 0.27 TC/m2/s (range, 0.04 to 0.53 TC/m2/s) when the empirical calculation method was used.(ABSTRACT TRUNCATED AT 250 WORDS) PMID:8250547

  3. Emission rates of sulfur dioxide, trace gases and metals from Mount Erebus, Antarctica

    NASA Astrophysics Data System (ADS)

    Kyle, Philip R.; Meeker, Kimberley; Finnegan, David

    1990-11-01

    SO2 emission rates have been measured annually since 1983 at Mount Erebus, Antarctica by correlation spectrometer (COSPEC V). Following a 4 month period of sustained strombolian activity in late 1984, SO2 emissions declined from 230 Mg/day in 1983 to 25 Mg/day and then slowly increased from 16 Mg/day in 1985 to 51 Mg/day in 1987. Nine sets of filter packs containing particle and (Li-7)OH treated filters were collected in the plume in 1986 and analyzed by neutron activation. Using the COSPEC data and measured element/S ratios on the filters, emission rates have been determined for trace gases and metals. HCl and HF emissions in 1983 are inferred to be about 1200 and 500 Mg/day, respectively. Mt. Erebus has therefore been an important source of halogens to the Antarctic atmosphere and could be responsible for excess Cl found in central Antarctica snow.

  4. Quasi-point incoherent ArF∗ excimer emission source at 193 nm using a laser-produced plasma

    NASA Astrophysics Data System (ADS)

    Kaku, M.; Sato, Y.; Kubodera, S.

    2012-04-01

    We have demonstrated proof-of-principle of an incoherent ArF∗ emission source with a quasi-point emission geometry using a laser-produced plasma in an Ar/F2/He/Ne mixed gas. The VUV emission characteristics, such as the emission size, were dependent on those of the plasma-initiating laser. The average emission power was 10 μW at a repetition rate of 10 Hz at 193 nm. The average power conversion efficiency of the 193-nm emission from the plasma-initiating Nd:YAG laser was 6.3×10-6. The average emission power at 193 nm was proportional to that of the plasma-initiating laser, indicating the scaling of the emission source.

  5. Dispersion from safety valves and other momentum emission sources: Continuous

    NASA Astrophysics Data System (ADS)

    Hanzevack, E. L.

    Safety valves are atypical pollutant emission sources in petroleum refineries and chemical plants. Their releases are characterized by very high velocities (from 20ms -1 to sonic) and near-ambient temperatures, so they are referred to as momentum sources, as opposed to bouyant sources. Since releases from these sources to the atmosphere may contain relatively high (often 100%) pollutant concentrations we have developed a method of accurately predicting the critical ground level concentrations of pollutants resulting from such sources. (The critical ground level concentration is the highest ambient pollutant concentration at any downwind location or meterological condition.) Since no data were available on which to base an air dispersion model for predicting ground level concentrations for momentum sources, an experimental program was undertaken, consisting of a full scale simulation of a momentum source emission using an inert tracer gas and downwind sampling to determine resulting critical ground level concentrations. Based on the data collected, a dispersion calculation method for estimating ground level concentrations from momentum sources was developed. The general form of this correlation is similar to the previously suggested, but not validated, American Society of Mechanical Engineers (ASME) momentum plume equation. The modified equation contains an additional parameter to account for the large gas density differences often encountered with momentum source releases. The equation was designed to be somewhat conservative to compensate for the randomness of atmospheric phenomena, the limited amount of experimental data, and the fact that safety valve releases can include dangerous substances. The calculation method described in this report is recommended to predict peak ambient concentrations for any source dominated by momentum plume conditions.

  6. Quantifying methane emissions and sources in the Colorado Front Range

    NASA Astrophysics Data System (ADS)

    Hughes, S.; Townsend-Small, A.; Schroeder, J.; Blake, N. J.; Blake, D. R.

    2016-12-01

    Methane is a powerful greenhouse gas and is relatively constant throughout the atmosphere, at 1.8 ppmv. This value, however, is increasing primarily due to anthropogenic sources, including agriculture and natural gas extraction. Here we present atmospheric methane fluxes measured during the Front Range Air Pollution and Photochemistry Experiment (FRAPPE) in July - August 2014 in the Colorado Front Range on the NCAR C-130. During this campaign 775 advanced whole air samples (AWAS) were collected onboard the aircraft and 248 samples were collected on the ground in order to quantify and evaluate air pollution sources. Methane concentrations were measured continuously aboard the aircraft using cavity ringdown spectroscopy. Major sources of methane in this region are oil and natural gas extraction and distribution, landfills, and cattle feed lots. In order to assess the impact of methane emissions on this area, methane flux was evaluated by comparing upwind and downwind concentrations where significant enhancements were observed downwind. We also present information from other hydrocarbons measured in canisters to attribute methane emissions to urban, agricultural, and oil and gas sources. The state of Colorado recently enacted legislation to reduce emissions of hydrocarbons from oil and gas facilities and our measurements will provide a preliminary estimate of whether these regulations are effective.

  7. Acidifier application rate impacts on ammonia emissions from US roaster chicken houses

    NASA Astrophysics Data System (ADS)

    Shah, Sanjay B.; Grimes, Jesse L.; Oviedo-Rondón, Edgar O.; Westerman, Philip W.

    2014-08-01

    Due to its potential environmental and public health impacts, emissions of ammonia (NH3) as well as several other gases from US livestock farms may be regulated. Broiler houses are important sources of NH3 emissions. However, there are no emissions data from roaster (8-12 wk old broilers, ˜4 kg ea.) houses. Producers treat the litter in broiler houses with acidifiers, such as sodium bisulfate (SBS, NaHSO4) to reduce ammonia production and protect bird health. However, there is very little data on the effect of acidifiers, particularly at high application rates on ammonia emissions. The impact of different SBS application rates [High (0.95-1.46 kg m-2, whole house), Medium (0.73 kg m-2, whole house), Low (0.37-0.49 kg m-2, whole house), and Control (0.37-0.49 kg m-2, brood chamber)] on ammonia emissions was evaluated in commercial roaster houses over 22 months spanning eight flocks. Ammonia emission from each fan was measured with an acid scrubber that operated only when the fan operated. Emissions were calculated using >95% measured data with the rest being estimated using robust methods. Exhaust ammonia-N concentrations were inversely correlated with the SBS application rates. Emission rates on animal unit (AU, where 1 AU = 500 kg live-mass) basis (ER, g d-1 AU-1) were reduced by 27, 13, and 5%, respectively, in the High, Medium, and Low treatments vs. the Control treatment (mean: 100 g d-1 AU-1, range: 86-114 g d-1 AU-1). Emission rates for the Control treatment measured in this study on roasters were mostly higher than ERs in the literature. Differences in ERs are not only due to diet, environmental and management conditions, but also due to measurement methods.

  8. Characterization of publication rotogravure press emission rates and compositions.

    PubMed

    Wadden, R A; Suero, M; Conroy, L M; Franke, J E; Scheff, P A

    2001-04-01

    Emission compositions and rates were determined during production for a publication rotogravure press room at a large rotogravure printing company. The press room housed a single 4-color, 8-print-stand press, with an 84" paper web. Average press speed was 1800 feet per minute. Data were collected over a 2-day period and included measurements of ventilation, room area concentrations, duct exhaust compositions, amount and composition of inks used, and worker exposures. These data were used with mass balance models that were appropriate for the workspace. Toluene comprised more than 90 percent of the inks and solvents and accounted for more than 90 percent of the press emissions. Average toluene emissions during press operation and press off conditions were 222 kg/hr and 8-38 kg/hr, respectively. The uncontrolled toluene emission on the basis of printed paper throughput was 3 g/m2. Of the total toluene released, 90 percent was captured by the local exhaust ventilation. The measured control efficiency was much lower than the average efficiency of 97 percent for the month of the test reported by the plant. A mass balance model evaluation demonstrated that only the lower efficiency was consistent with measured room concentrations. Using the measured emission rates and actual monthly press on and press off conditions, the difference in efficiency for the plant (10 rotogravure presses) extrapolates to the additional release to the workspace and ambient environment of over 700 tons/yr of toluene.

  9. Accurate Simulation of Acoustic Emission Sources in Composite Plates

    NASA Technical Reports Server (NTRS)

    Prosser, W. H.; Gorman, M. R.

    1994-01-01

    Acoustic emission (AE) signals propagate as the extensional and flexural plate modes in thin composite plates and plate-like geometries such as shells, pipes, and tubes. The relative amplitude of the two modes depends on the directionality of the source motion. For source motions with large out-of-plane components such as delaminations or particle impact, the flexural or bending plate mode dominates the AE signal with only a small extensional mode detected. A signal from such a source is well simulated with the standard pencil lead break (Hsu-Neilsen source) on the surface of the plate. For other sources such as matrix cracking or fiber breakage in which the source motion is primarily in-plane, the resulting AE signal has a large extensional mode component with little or no flexural mode observed. Signals from these type sources can also be simulated with pencil lead breaks. However, the lead must be fractured on the edge of the plate to generate an in-plane source motion rather than on the surface of the plate. In many applications such as testing of pressure vessels and piping or aircraft structures, a free edge is either not available or not in a desired location for simulation of in-plane type sources. In this research, a method was developed which allows the simulation of AE signals with a predominant extensional mode component in composite plates requiring access to only the surface of the plate.

  10. Polychlorinated Biphenyl Sources, Emissions, and Environmental Levels in School Buildings

    EPA Science Inventory

    Building materials and components containing polychlorinated biphenyls (PCBs) were used in some U.S. school buildings until the late 1970s and may be present today. PCB emission rates from caulk and fluorescent light ballasts were measured in laboratory chambers. PCB concentrat...

  11. Polychlorinated Biphenyl Sources, Emissions, and Environmental Levels in School Buildings

    EPA Science Inventory

    Building materials and components containing polychlorinated biphenyls (PCBs) were used in some U.S. school buildings until the late 1970s and may be present today. PCB emission rates from caulk and fluorescent light ballasts were measured in laboratory chambers. PCB concentrat...

  12. Determination of Summertime VOC Emission Rates from Produced Water Ponds in the Uintah Basin

    NASA Astrophysics Data System (ADS)

    Martin, R. S.; Woods, C.; Lyman, S.

    2013-12-01

    The observance of excess ozone concentrations in Utah's Uintah Basin over past several years has prompted several investigations into the extent and causes of the elevated ozone. Among these is the assessment of potential emissions of reactive VOCs. Evaporation ponds, used a remediation technique for treatment of contaminated production and other waters, are one potential source of significant VOC emissions and is estimated that there are around 160 such ponds within the Uintah Basin's oil and gas production areas. In June 2012 VOC emission rates for several reactive VOCs were derived for an evaporation facility consisting of a small inlet pond (≈0.03 acres) and two larger, serial ponds (≈4.3 acres each). The emission rates were determined over three sampling periods using an inverse modeling approach. Under this methodology, ambient VOC concentrations are determined at several downwind locations through whole-air collection into SUMMA canisters, followed by GC/MS quantification and compared with predicted concentrations using an EPA-approved dispersion model, AERMOD. The presumed emission rates used within the model were then adjusted until the modeled concentrations approach the observed concentrations. The derived emission rates for the individual VOCs were on the order of 10-3 g/s/m2 from the inlet pond and 10-6 g/s/m2 from the larger ponds. The emissions from the 1st pond in series after the inlet pond were about 3-4x the emissions from the 2nd pond. These combined emission rates are about an order of magnitude those reported for a single study in Colorado (Thoma, 2009). It should be noted, however, that the variability about each of the VOC emission rates was significant (often ×100% at the 95% confidence interval). Extrapolating these emission rates to the estimated total areas of all the evaporation ponds within Basin resulted in calculated Basin-wide VOC emissions 292,835 tons/yr. However, Bar-Ilan et al. (2009) estimated 2012 VOC oil and gas related

  13. The infrared emission bands. III. Southern IRAS sources.

    PubMed

    Cohen, M; Tielens, A G; Bregman, J; Witteborn, F C; Rank, D M; Allamandola, L J; Wooden, D H; de Muizon, M

    1989-06-01

    We present airborne 5-8 micrometers spectra of southern IRAS sources which reveal strong polycyclic aromatic hydrocarbon (PAH) emission features. The good correlation between the bands, in particular the dominant 6.2 and "7.7" micrometers features, strongly imply a common carrier, reinforcing the PAH hypothesis. However, small but detectable spectral variations exist. Planetaries have a distinctly different ratio of I(6.2)/I(7.7) than other nebulae, accompanied by a redward shift in the actual wavelength of the "7.7" micrometers peak. Further, we have detected a new feature, previously predicted from laboratory spectra of PAH molecules, at 5.2 micrometers in many of these sources. Spectra of two rare [WC 10] planetary nebular nuclei indicate a very prominent plateau of emission, linking the 6.2 and 7.7 micrometers bands. Several of our sources show definite evidence for emission structure between 14 and 23 micrometers in their IRAS Low-Resolution Spectral Atlas spectra: we attribute this structure to PAH bands. too. We have defined the "generic" spectrum of emission bands relating the mean intensities of each band to that of the strongest, near 7.7 micrometers. We have added three more planetary or protoplanetary nebulae to our correlation between 7.7 micrometers band intensity and nebular gas phase C/O ratio, namely NGC 6302, HR 4049, and the highly carbon-rich [WC 10] nucleus, CPD--56 degrees 8032. For the latter we have determined a ratio for C/O of approximately 4.8 from IUE observations. The good correlation between the intensity ratio of the "7.7" micrometers feature relative to the far-infrared dust continuum and nebular C/O also supports a carbonaceous carrier for these emission features.

  14. Footprint methods to separate N2O emission rates from adjacent paddock areas.

    PubMed

    Mukherjee, Sandipan; McMillan, Andrew M S; Sturman, Andrew P; Harvey, Mike J; Laubach, Johannes

    2015-03-01

    Using micrometeorological techniques to measure greenhouse gas emissions from differently treated adjacent plots is a promising avenue to verify the effect of mitigation strategies at the field scale. In pursuing such an approach, it is crucial to accurately characterize the source area of the fluxes measured at each sampling point. Hence, a comprehensive footprint analysis method is required so that emission rates can be obtained for a specific field within a biochemically heterogeneous area. In this study, a footprint analysis method is developed to estimate the emission for an experiment where the flux of N2O is measured from several control and treated plots. The emission rate of an individual plot is estimated using an inverse footprint fraction approach where the footprint fractions are obtained from an analytical footprint model. A numerical solution for obtaining the background flux for such a multiplot measurement system is also provided. Results of the footprint analysis method are assessed, first, by comparing footprint fractions obtained from both an analytical footprint model and a "forward" simulation of a backward Lagrangian stochastic (bLs) model; and second, by comparing the emission rates of a control plot obtained from the footprint analysis method and from the "backward" simulation of the bLs model. It is found that the analytical footprint fractions compare well with the values obtained from the bLs model (correlation coefficient of 0.58 and 0.66 within p value <0.001). An average of 4.3 % of the measured fluxes is found to be contributed by sources outside the measured area and, excluding this outside area contribution to the measured flux, footprint corrected emission rates within the defined domain are found to increase by 2.1 to 5.8 % of the measured flux. Also, the proposed method of emission rate estimation is found to work well under a wide range of atmospheric stability.

  15. Footprint methods to separate N2O emission rates from adjacent paddock areas

    NASA Astrophysics Data System (ADS)

    Mukherjee, Sandipan; McMillan, Andrew M. S.; Sturman, Andrew P.; Harvey, Mike J.; Laubach, Johannes

    2015-03-01

    Using micrometeorological techniques to measure greenhouse gas emissions from differently treated adjacent plots is a promising avenue to verify the effect of mitigation strategies at the field scale. In pursuing such an approach, it is crucial to accurately characterize the source area of the fluxes measured at each sampling point. Hence, a comprehensive footprint analysis method is required so that emission rates can be obtained for a specific field within a biochemically heterogeneous area. In this study, a footprint analysis method is developed to estimate the emission for an experiment where the flux of N2O is measured from several control and treated plots. The emission rate of an individual plot is estimated using an inverse footprint fraction approach where the footprint fractions are obtained from an analytical footprint model. A numerical solution for obtaining the background flux for such a multiplot measurement system is also provided. Results of the footprint analysis method are assessed, first, by comparing footprint fractions obtained from both an analytical footprint model and a "forward" simulation of a backward Lagrangian stochastic (bLs) model; and second, by comparing the emission rates of a control plot obtained from the footprint analysis method and from the "backward" simulation of the bLs model. It is found that the analytical footprint fractions compare well with the values obtained from the bLs model (correlation coefficient of 0.58 and 0.66 within p value <0.001). An average of 4.3 % of the measured fluxes is found to be contributed by sources outside the measured area and, excluding this outside area contribution to the measured flux, footprint corrected emission rates within the defined domain are found to increase by 2.1 to 5.8 % of the measured flux. Also, the proposed method of emission rate estimation is found to work well under a wide range of atmospheric stability.

  16. Biophoton emission. New evidence for coherence and DNA as source.

    PubMed

    Popp, F A; Nagl, W; Li, K H; Scholz, W; Weingärtner, O; Wolf, R

    1984-03-01

    The phenomenon of ultraweak photon emission from living systems was further investigated in order to elucidate the physical properties of this radiation and its possible source. We obtained evidence that the light has a high degree of coherence because of (1) its photon count statistics, (2) its spectral distribution, (3) its decay behavior after exposure to light illumination, and (4) its transparency through optically thick materials. Moreover, DNA is apparently at least an important source, since conformational changes induced with ethidium bromide in vivo are clearly reflected by changes of the photon emission of cells. The physical properties of the radiation are described, taking DNA as an exciplex laser system, where a stable state can be reached far from thermal equilibrium at threshold.

  17. Indoor aldehydes concentration and emission rate of formaldehyde in libraries and private reading rooms

    NASA Astrophysics Data System (ADS)

    Kim, Jeonghoon; Kim, Seojin; Lee, Kiyoung; Yoon, Dongwon; Lee, Jiryang; Ju, DaeYoung

    2013-06-01

    Aldehydes are of particularly interest due to their potential adverse impact on human health. Formaldehyde is one of the most abundant indoor pollutants. To improve indoor air quality, identifying and removing the major emission sources of formaldehyde would be desirable. The purposes of this study were to determine aldehyde concentrations in libraries and reading rooms and to identify emission sources of formaldehyde in private reading rooms. Indoor aldehyde concentrations were quantified at 66 facilities, including public libraries, children's libraries, public reading rooms, and private reading rooms, in the Seoul metropolitan area. Emission fluxes of formaldehyde from the surfaces of desks, chairs, floors, walls, and ceilings in 19 private reading rooms were measured using a passive emission colorimetric sensor. Indoor aldehyde (formaldehyde, acetaldehyde, propioaldehyde, benzaldehyde, and hexaldehyde) levels were significantly higher than outdoor levels. Indoor formaldehyde geometric mean concentrations in private reading rooms (119.3 μg m-3) were significantly higher than in public libraries (29.2 μg m-3), children's libraries (29.3 μg m-3), and public reading rooms (40.8 μg m-3). Indoor formaldehyde levels were associated with relative humidity. In private reading rooms, the emission rates from desks (255.5 ± 214.8 μg h-1) and walls (231.7 ± 192.3 μg h-1) were significantly higher than that from chairs (79.6 ± 88.5 μg h-1). Desks (31%) and walls (29%) were the major emission sources of formaldehyde in 14 facilities in which measurements exceeded the indoor standard of 100 μg m-3. The age of interior materials was a significant factor for indoor formaldehyde emission flux. Controlling the emission rates of desks and walls is recommended to improve formaldehyde concentrations in private reading rooms.

  18. Global High-Resolution Emission Inventories from Combustion Sources

    NASA Astrophysics Data System (ADS)

    Tao, S.; Huang, Y.; Chen, H.; Shen, H.

    2014-12-01

    A series efforts have been made to reduce uncertainty of emission inventories from combustion sources. The inventories developed are highly resolved spatially (0.1 degree), temporally (monthly or daily), and sectorically (over 60 combustion sources). Sub-national, instead of national fuel data are used to reduce spatial bias due to uneven distribution of per person energy consumption within large countries. Space-for-time substitution method was developed to model the dependence of residential energy consumptions on a series of meteorological and socioeconomic conditions. The regression models were used to project temporal variation of energy consumption, subsequently emissions of greenhouse gases and air pollutants. The models can also be used to downscale spatial distribution of residential emissions. By using this approach, global emission inventories of black carbon, polycyclic aromatic hydrocarbons, mercury, TSP, PM10, and PM2.5 have been established. The inventories were used to potential health impact assessment, atmospheric transport and long-range transport modeling, as well as exposure and health impact modeling.

  19. NUclei of GAlaxies. V. Radio emission in 7 NUGA sources

    NASA Astrophysics Data System (ADS)

    Krips, M.; Eckart, A.; Krichbaum, T. P.; Pott, J.-U.; Leon, S.; Neri, R.; García-Burillo, S.; Combes, F.; Boone, F.; Baker, A. J.; Tacconi, L. J.; Schinnerer, E.; Hunt, L. K.

    2007-03-01

    We present high angular resolution radio snap-shot observations of seven nearby low-luminosity active galaxies (LLAGN) from the NUclei of GAlaxies (NUGA) survey. The observations were conducted with MERLIN and EVN/VLBI at 18 cm and 6 cm. At all observed angular resolutions and frequencies, we find indications for extended emission in about ~40% of the sources, consistent with the decrease of flux with increasing angular resolution. The extended components resemble jet emission in a majority of cases, consistent with the optically thin synchrotron emission implied by their steep spectra. We consider the compact 6 cm EVN/VLBI radio emission of our sources in the context of the "fundamental plane" that previous LLAGN studies identified within the three-dimensional parameter space of radio luminosity, X-ray luminosity, and black hole mass. We demonstrate, using NGC 7217 and NGC 1068 as particular examples, that high-resolution, multi-epoch radio observations offer useful information about the origin of offsets from the fundamental plane. EVN: The European VLBI Network is a joint facility of European, Chinese, South African and other radio astronomy institutes funded by their national research councils. MERLIN is a national facility operated by the University of Manchester on behalf of PPARC. VLBI including the VLBA: The National Radio Astronomy Observatory is a facility of the National Science Foundation operated under cooperative agreement by Associated Universities, Inc.

  20. A measurement system for alpha and beta surface emission rate using MWPC

    NASA Astrophysics Data System (ADS)

    Lin, Ye; Fang, Fang; Ren, Jia-Fu; He, Lin-Feng; Tang, Fang-Dong; Xu, Yi-He; Ding, Wei-Cheng

    2015-05-01

    We have developed a large area multi-wire proportional counter (MWPC) as a standard for the measurement of alpha and beta surface emission rate at the Shanghai Institute of Measurement and Testing Technology (SIMT). To shorten the preparation time for chamber gas refilling, a self-designed gas control unit was adopted. Various characteristics of the system have been studied. The uncertainties were analysed. Three certified alpha plane sources (Am-241) and six certified beta plane sources (Tl-204 and Sr-90/Y-90) were measured by this system. The results show excellent agreement with the surface emission rate reported by the National Institute of Measuring, China (NIM) that En values of all measured sources are within ±1. Supported by National Natural Science Foundation of China (41204133)

  1. Suppression of emission rates improves sonar performance by flying bats.

    PubMed

    Adams, Amanda M; Davis, Kaylee; Smotherman, Michael

    2017-01-31

    Echolocating bats face the challenge of actively sensing their environment through their own emissions, while also hearing calls and echoes of nearby conspecifics. How bats mitigate interference is a long-standing question that has both ecological and technological implications, as biosonar systems continue to outperform man-made sonar systems in noisy, cluttered environments. We recently showed that perched bats decreased calling rates in groups, displaying a behavioral strategy resembling the back-off algorithms used in artificial communication networks to optimize information throughput at the group level. We tested whether free-tailed bats (Tadarida brasiliensis) would employ such a coordinated strategy while performing challenging flight maneuvers, and report here that bats navigating obstacles lowered emission rates when hearing artificial playback of another bat's calls. We measured the impact of acoustic interference on navigation performance and show that the calculated reductions in interference rates are sufficient to reduce interference and improve obstacle avoidance. When bats flew in pairs, each bat responded to the presence of the other as an obstacle by increasing emissions, but hearing the sonar emissions of the nearby bat partially suppressed this response. This behavior supports social cohesion by providing a key mechanism for minimizing mutual interference.

  2. Suppression of emission rates improves sonar performance by flying bats

    PubMed Central

    Adams, Amanda M.; Davis, Kaylee; Smotherman, Michael

    2017-01-01

    Echolocating bats face the challenge of actively sensing their environment through their own emissions, while also hearing calls and echoes of nearby conspecifics. How bats mitigate interference is a long-standing question that has both ecological and technological implications, as biosonar systems continue to outperform man-made sonar systems in noisy, cluttered environments. We recently showed that perched bats decreased calling rates in groups, displaying a behavioral strategy resembling the back-off algorithms used in artificial communication networks to optimize information throughput at the group level. We tested whether free-tailed bats (Tadarida brasiliensis) would employ such a coordinated strategy while performing challenging flight maneuvers, and report here that bats navigating obstacles lowered emission rates when hearing artificial playback of another bat’s calls. We measured the impact of acoustic interference on navigation performance and show that the calculated reductions in interference rates are sufficient to reduce interference and improve obstacle avoidance. When bats flew in pairs, each bat responded to the presence of the other as an obstacle by increasing emissions, but hearing the sonar emissions of the nearby bat partially suppressed this response. This behavior supports social cohesion by providing a key mechanism for minimizing mutual interference. PMID:28139707

  3. UV emissions from low energy artificial light sources.

    PubMed

    Fenton, Leona; Moseley, Harry

    2014-01-01

    Energy efficient light sources have been introduced across Europe and many other countries world wide. The most common of these is the Compact Fluorescent Lamp (CFL), which has been shown to emit ultraviolet (UV) radiation. Light Emitting Diodes (LEDs) are an alternative technology that has minimal UV emissions. This brief review summarises the different energy efficient light sources available on the market and compares the UV levels and the subsequent effects on the skin of normal individuals and those who suffer from photodermatoses. © 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

  4. Determination of VOC emission rates and compositions for offset printing.

    PubMed

    Wadden, R A; Scheff, P A; Franke, J E; Conroy, L M; Keil, C B

    1995-07-01

    The release rates of volatile organic compounds (VOC) as fugitive emissions from offset printing are difficult to quantify, and the compositions are usually not known. Tests were conducted at three offset printing shops that varied in size and by process. In each case, the building shell served as the test "enclosure," and air flow and concentration measurements were made at each air entry and exit point. Emission rates and VOC composition were determined during production for (1) a small shop containing three sheetfed presses and two spirit duplicators (36,700 sheets, 47,240 envelopes and letterheads), (2) a medium-size industrial in-house shop with two webfed and three sheetfed presses, and one spirit duplicator (315,130 total sheets), and (3) one print room of a large commercial concern containing three webfed, heatset operations (1.16 x 10(6) ft) served by catalytic air pollution control devices. Each test consisted of 12 one-hour periods over two days. Air samples were collected simultaneously during each period at 7-14 specified locations within each space. The samples were analyzed by gas chromatography (GC) for total VOC and for 13-19 individual organics. Samples of solvents used at each shop were also analyzed by GC. Average VOC emission rates were 4.7-6.1 kg/day for the small sheetfed printing shop, 0.4-0.9 kg/day for the industrial shop, and 79-82 kg/day for the commercial print room. Emission compositions were similar and included benzene, toluene, xylenes, ethylbenzene, and hexane. Comparison of the emission rates with mass balance estimates based on solvent usage and composition were quite consistent.(ABSTRACT TRUNCATED AT 250 WORDS)

  5. Mitigation strategies for methane emissions from agricultural sources

    SciTech Connect

    Duxbury, J.M.

    1993-12-31

    Anthropogenic emissions of CH{sub 4} account for 70% of total global emissions of this greenhouse gas. Current anthropogenic emissions of CH{sub 4} in the US are estimated to be between 24-30 Tg CH{sub 4} or 7-9% of the global anthropogenic total. By comparison the US is responsible for 27% of anthropogenic emissions of CO{sub 2} from fossil fuel use. Table 1 shows that the major anthropogenic sources of CH{sub 4} in the US are landfills (37%), domestic livestock and livestock waste (31%) and the coal mining/natural gas/petroleum industries (28%). On a global basis it is estimated that US landfills contribute 30% to the global landfill total, whereas livestock (including waste) and the coal mining/natural gas/petroleum industries each contribute about 8% to their respective global totals. The US is an insignificant contributor (< 1%) to global emissions of CH{sub 4} from rice paddies.

  6. Carbonyl emissions from vehicular exhausts sources in Hong Kong.

    PubMed

    Ho, Steven Sai Hang; Ho, Kin Fai; Lee, Shun Cheng; Cheng, Yan; Yu, Jian Zhen; Lam, Ka Man; Feng, Natale Sin Yau; Huang, Yu

    2012-02-01

    Vehicular emission (VE) is one of the important anthropogenic sources for airborne carbonyls in urban area. Six types of VE-dominated samples were collected at representative locations in Hong Kong where polluted by a particular fueled type of vehicles, including (i) a gas refilling taxis station (liquefied petroleum gas [LPG] emission); (ii) a light-duty passenger car park (gasoline emission); (iii) a minibus station (diesel emission); (iv) a single-deck-bus depot (diesel emission); (v) a double-deck-bus depot (diesel emission); and (vi) a whole-food market entrance for light- and heavy-duty vehicles (diesel emission). A total of 15 carbonyls in the samples were quantified. Formaldehyde was the most abundant carbonyl among the VE-dominated samples, and its contribution to the total quantified amount on a molar basis ranged from 54.8% to 60.8%. Acetaldehyde and acetone were the next two abundant carbonyls. The carbonyls were quantified at three roadside locations in Hong Kong. The highest concentrations of formaldehyde and acetaldehyde, 22.7 +/- 8.4 and 6.0 +/- 2.8 microg/m3, respectively, were determined in the samples collected at a main transportation gate for goods between Hong Kong and Mainland China. The total quantified carbonyl concentration, 37.9 +/- 9.3 microg/m3, was the highest at an entrance of a cross-harbor tunnel in downtown area. The theoretical carbonyls compositions of the three roadside locations were estimated according to the VE-dominated sample profiles and the statistics on vehicle numbers and types during the sampling period. The measured compositions of formaldehyde were much higher than the theoretical compositions in summer, demonstrating that photochemical reactions significantly contributed to the formaldehyde production in the roadsides.

  7. Modeling Atmospheric Emissions and Calculating Mortality Rates Associated with High Volume Hydraulic Fracturing Transportation

    NASA Astrophysics Data System (ADS)

    Mathews, Alyssa

    Emissions from the combustion of fossil fuels are a growing pollution concern throughout the global community, as they have been linked to numerous health issues. The freight transportation sector is a large source of these emissions and is expected to continue growing as globalization persists. Within the US, the expanding development of the natural gas industry is helping to support many industries and leading to increased transportation. The process of High Volume Hydraulic Fracturing (HVHF) is one of the newer advanced extraction techniques that is increasing natural gas and oil reserves dramatically within the US, however the technique is very resource intensive. HVHF requires large volumes of water and sand per well, which is primarily transported by trucks in rural areas. Trucks are also used to transport waste away from HVHF well sites. This study focused on the emissions generated from the transportation of HVHF materials to remote well sites, dispersion, and subsequent health impacts. The Geospatial Intermodal Freight Transport (GIFT) model was used in this analysis within ArcGIS to identify roadways with high volume traffic and emissions. High traffic road segments were used as emissions sources to determine the atmospheric dispersion of particulate matter using AERMOD, an EPA model that calculates geographic dispersion and concentrations of pollutants. Output from AERMOD was overlaid with census data to determine which communities may be impacted by increased emissions from HVHF transport. The anticipated number of mortalities within the impacted communities was calculated, and mortality rates from these additional emissions were computed to be 1 in 10 million people for a simulated truck fleet meeting stricter 2007 emission standards, representing a best case scenario. Mortality rates due to increased truck emissions from average, in-use vehicles, which represent a mixed age truck fleet, are expected to be higher (1 death per 341,000 people annually).

  8. Sources of variation in waterfowl survival rates

    USGS Publications Warehouse

    Krementz, D.G.; Barker, R.J.; Nichols, J.D.

    1997-01-01

    Because of the need to manage hunted populations of waterfowl (Anatidae), biologists have studied many demographic traits of waterfowl by analyzing band recoveries. These analyses have produced the most extensive and best estimates of survival available for any group of birds. Using these data, we examined several factors that might explain variation among annual survival rates to explore large-scale patterns that might be useful in understanding waterfowl population dynamics. We found that geography, body mass, and tribe (i.e. phylogeny) were important in explaining variation in average waterfowl survival rates.

  9. Sources of variation in waterfowl survival rates

    USGS Publications Warehouse

    Krementz, D.G.; Barker, R.J.; Nichols, J.D.

    1997-01-01

    Because of the need to manage hunted populations of waterfowl (Anatidae), biologists have studied many demographic traits of waterfowl by analyzing band recoveries. These analyses have produced the most extensive and best estimates of survival available for any group of birds. Using these data, we examined several factors that might explain variation among annual survival rates to explore large-scale patterns that might be useful in understanding waterfowl population dynamics. We found that geography, body mass, and tribe (i.e. phylogeny) were important in explaining variation in average waterfowl survival rates.

  10. Acoustic emission strand burning technique for motor burning rate prediction

    NASA Technical Reports Server (NTRS)

    Christensen, W. N.

    1978-01-01

    An acoustic emission (AE) method is being used to measure the burning rate of solid propellant strands. This method has a precision of 0.5% and excellent burning rate correlation with both subscale and large rocket motors. The AE procedure burns the sample under water and measures the burning rate from the acoustic output. The acoustic signal provides a continuous readout during testing, which allows complete data analysis rather than the start-stop clockwires used by the conventional method. The AE method helps eliminate such problems as inhibiting the sample, pressure increase and temperature rise, during testing.

  11. Isoprene and terpenoid emissions from Abies alba: Identification and emission rates under ambient conditions

    NASA Astrophysics Data System (ADS)

    Pokorska, Olga; Dewulf, Jo; Amelynck, Crist; Schoon, Niels; Šimpraga, Maja; Steppe, Kathy; Van Langenhove, Herman

    2012-11-01

    In this study, biogenic volatile organic compound (BVOC) emissions from Abies alba were studied under ambient conditions in Flanders (Belgium). Emission patterns and rates were investigated from April till November 2010 by using the dynamic branch enclosure technique. The present work revealed that A. alba is an isoprene emitter, with isoprene accounting for 86-93% of total BVOC emissions, except during budburst (67%) in May. The emission spectrum of A. alba consisted of 27 compounds. Next to isoprene, the main emitted compounds were α-pinene, β-pinene, camphene and limonene. BVOC emissions showed a peak in June after development of the young needles, followed by a constant emission during summer months and September and a decrease in October. In all the samples isoprene was the most abundant compound with standardized emission rates between 27 μg g(dw)-1 h-1 in June and 4.6 μg g(dw)-1 h-1 in October, while the total standardized terpenoid emission rates ranged from 2.85 μg g(dw)-1 h-1 in June to 0.26 μg g(dw)-1 h-1 in October. The obtained average β coefficients according to the temperature dependent algorithm of Guenther et al. (1993) during April-June, July, August and September-October were as follows: for terpenoids 0.12 ± 0.03, 0.11 ± 0.05, 0.12 ± 0.04, 0.24 ± 0.01 K-1 and sesquiterpenes (SQTs) 0.09 ± 0.02, 0.11 ± 0.01, 0.10 ± 0.05, 0 K-1, respectively. Overall, isoprene detected in this study was never quantified in previous studies on A. alba and this finding could have a significant impact on the regional BVOCs budget. Therefore, the result of this study is very important for modeling and local air quality.

  12. Biomass Burning Emissions of Black Carbon from African Sources

    NASA Astrophysics Data System (ADS)

    Aiken, A. C.; Leone, O.; Nitschke, K. L.; Dubey, M. K.; Carrico, C.; Springston, S. R.; Sedlacek, A. J., III; Watson, T. B.; Kuang, C.; Uin, J.; McMeeking, G. R.; DeMott, P. J.; Kreidenweis, S. M.; Robinson, A. L.; Yokelson, R. J.; Zuidema, P.

    2016-12-01

    Biomass burning (BB) emissions are a large source of carbon to the atmosphere via particles and gas phase species. Carbonaceous aerosols are emitted along with gas-phase carbon monoxide (CO) and carbon dioxide (CO2) that can be used to determine particulate emission ratios and modified combustion efficiencies. Black carbon (BC) aerosols are potentially underestimated in global models and are considered to be one of the most important global warming factors behind CO2. Half or more BC in the atmosphere is from BB, estimated at 6-9 Tg/yr (IPCC, 5AR) and contributing up to 0.6 W/m2 atmospheric warming (Bond et al., 2013). With a potential rise in drought and extreme events in the future due to climate change, these numbers are expected to increase. For this reason, we focus on BC and organic carbon aerosol species that are emitted from forest fires and compare their emission ratios, physical and optical properties to those from controlled laboratory studies of single-source BB fuels to understand BB carbonaceous aerosols in the atmosphere. We investigate BC in concentrated BB plumes as sampled from the new U.S. DOE ARM Program campaign, Layered Atlantic Smoke Interactions with Clouds (LASIC). The ARM Aerosol Mobile Facility 1 (AMF1) and Mobile Aerosol Observing System (MAOS) are currently located on Ascension Island in the South Atlantic Ocean, located midway between Angola and Brazil. The location was chosen for sampling maximum aerosol outflow from Africa. The far-field aged BC from LASIC is compared to BC from indoor generation from single-source fuels, e.g. African grass, sampled during Fire Lab At Missoula Experiments IV (FLAME-IV). BC is measured with a single-particle soot photometer (SP2) alongside numerous supporting instrumentation, e.g. particle counters, CO and CO2 detectors, aerosol scattering and absorption measurements, etc. FLAME-IV includes both direct emissions and well-mixed aerosol samples that have undergone dilution, cooling, and condensation. BC

  13. Atmospheric Pollution and Emission Sources in South Asian Urban Region

    NASA Astrophysics Data System (ADS)

    Biswas, K. F.; Husain, Liaquat

    2009-04-01

    Rapid urbanization, and lack of efficient monitoring and control of pollution, along with phenomena like Asian Brown Haze or prolonged episodes of winter fog, makes the South Asian atmospheric chemistry a very complex one. The anthropogenic aerosols released from this region are projected to become the dominant component of anthropogenic aerosols worldwide in the next 25 years (Nakicenovic and Swart, 2000). The region is one of the most densely populated in the world, with present population densities of 100-500 persons km-2. There are six big cities, namely, Delhi, Dhaka, Karachi, Kolkata, Lahore, and Mumbai, each housing a population around or above 10 million. There is now a real concern about the sustainability of the region's ability to support the population due to air pollution, loss of biodiversity and soil degradation. Therefore, we conducted several extensive campaigns over last 10 years in Lahore, Karachi, and Islamabad in Pakistan to (1) chemically characterize the aerosols (PM2.5 mass, concentrations of trace elements, ions, black and organic carbon), and gaseous pollutants (concentrations of NH3, SO2, HONO, HNO3, HCl and (COOH)2, and (2) identify the major emission sources in this region. Exceedingly high concentrations of all species, relative to major urban areas of US and Europe, were observed. Concentrations of PM2.5, BC, Pb, SO42-, NH4+, HONO, NH3 respectively, up to 476, 110, 12, 66, 60, 19.6 and 50 μgm-3 were observed in these cities, which were far in excess of WHO and US EPA air quality standard (Biswas et al., 2008). We use air parcel back trajectories, intercomponent relationships and meteorological observations to explain chemistry and emission sources of aerosol constituents. Carbonaceous aerosols contributed up to 69% of the PM2.5 mass (Husain et al., 2007). Source apportionment was conducted using positive matrix factorization. The analysis has classified six emission sources of aerosol components, namely, industrial activities, wood

  14. A global gas flaring black carbon emission rate dataset from 1994 to 2012

    PubMed Central

    Huang, Kan; Fu, Joshua S.

    2016-01-01

    Global flaring of associated petroleum gas is a potential emission source of particulate matters (PM) and could be notable in some specific regions that are in urgent need of mitigation. PM emitted from gas flaring is mainly in the form of black carbon (BC), which is a strong short-lived climate forcer. However, BC from gas flaring has been neglected in most global/regional emission inventories and is rarely considered in climate modeling. Here we present a global gas flaring BC emission rate dataset for the period 1994–2012 in a machine-readable format. We develop a region-dependent gas flaring BC emission factor database based on the chemical compositions of associated petroleum gas at various oil fields. Gas flaring BC emission rates are estimated using this emission factor database and flaring volumes retrieved from satellite imagery. Evaluation using a chemical transport model suggests that consideration of gas flaring emissions can improve model performance. This dataset will benefit and inform a broad range of research topics, e.g., carbon budget, air quality/climate modeling, and environmental/human exposure. PMID:27874852

  15. A global gas flaring black carbon emission rate dataset from 1994 to 2012

    NASA Astrophysics Data System (ADS)

    Huang, Kan; Fu, Joshua S.

    2016-11-01

    Global flaring of associated petroleum gas is a potential emission source of particulate matters (PM) and could be notable in some specific regions that are in urgent need of mitigation. PM emitted from gas flaring is mainly in the form of black carbon (BC), which is a strong short-lived climate forcer. However, BC from gas flaring has been neglected in most global/regional emission inventories and is rarely considered in climate modeling. Here we present a global gas flaring BC emission rate dataset for the period 1994-2012 in a machine-readable format. We develop a region-dependent gas flaring BC emission factor database based on the chemical compositions of associated petroleum gas at various oil fields. Gas flaring BC emission rates are estimated using this emission factor database and flaring volumes retrieved from satellite imagery. Evaluation using a chemical transport model suggests that consideration of gas flaring emissions can improve model performance. This dataset will benefit and inform a broad range of research topics, e.g., carbon budget, air quality/climate modeling, and environmental/human exposure.

  16. A global gas flaring black carbon emission rate dataset from 1994 to 2012.

    PubMed

    Huang, Kan; Fu, Joshua S

    2016-11-22

    Global flaring of associated petroleum gas is a potential emission source of particulate matters (PM) and could be notable in some specific regions that are in urgent need of mitigation. PM emitted from gas flaring is mainly in the form of black carbon (BC), which is a strong short-lived climate forcer. However, BC from gas flaring has been neglected in most global/regional emission inventories and is rarely considered in climate modeling. Here we present a global gas flaring BC emission rate dataset for the period 1994-2012 in a machine-readable format. We develop a region-dependent gas flaring BC emission factor database based on the chemical compositions of associated petroleum gas at various oil fields. Gas flaring BC emission rates are estimated using this emission factor database and flaring volumes retrieved from satellite imagery. Evaluation using a chemical transport model suggests that consideration of gas flaring emissions can improve model performance. This dataset will benefit and inform a broad range of research topics, e.g., carbon budget, air quality/climate modeling, and environmental/human exposure.

  17. Reactive trace gas emissions from stressed plants: a poorly characterized major source of atmospheric volatiles

    NASA Astrophysics Data System (ADS)

    Niinemets, Ülo

    2017-04-01

    Vegetation constitutes the greatest source of reactive volatile organic compounds in the atmosphere. The current emission estimates primarily rely on constitutive emissions that are present only in some plant species. However, all plant species can be induced to emit reactive volatiles by different abiotic and biotic stresses, but the stress-dependent emissions have been largely neglected in emission measurements and models. This presentation provides an overview of systematic screening of stress-dependent volatile emissions from a broad range of structurally and physiologically divergent plant species from temperate to tropical ecosystems. Ozone, heat, drought and wounding stress were the abiotic stresses considered in the screening, while biotic stress included herbivory, chemical elicitors simulating herbivory and fungal infections. The data suggest that any moderate to severe stress leads to significant emissions of a rich blend of volatiles, including methanol, green leaf volatiles (the lipoxygenase pathway volatiles, dominated by C6 aldehydes, alcohols and derivatives), different mono- and sesquiterpenes and benzenoids. The release of volatiles occurs in stress severity-dependent manner, although the emission responses are often non-linear with more severe stresses resulting in disproportionately greater emissions. Stress volatile release is induced in both non-constitutive and constitutive volatile emitters, whereas the rate of constitutive volatile emissions in constitutive emitters is often reduced under environmental and biotic stresses. Given that plants in natural conditions often experience stress, this analysis suggests that global volatile emissions have been significantly underestimated. Furthermore, in globally changing hotter climates, the frequency and severity of both abiotic and biotic stresses is expected to increase. Thus, the stress-induced volatile emissions are predicted to play a dominant role in plant-atmosphere interactions in near

  18. Plasma emission spectroscopy for operating and developing the Spallation Neutron Source (SNS) H- ion sources

    SciTech Connect

    Han, Baoxi; Welton, Robert F; Murray Jr, S N; Pennisi, Terry R; Santana, Manuel; Stockli, Martin P

    2014-01-01

    An RF-driven, Cs-enhanced H- ion source feeds the SNS accelerator with a high current (typically >50 mA), ~1.0 ms pulsed beam at 60 Hz. To achieve the persistent high current beam for several weeks long service cycles, each newly installed ion source undergoes a rigorous conditioning and cesiation processes. Plasma conditioning outgases the system and sputter-cleans the ion conversion surfaces. A cesiation process immediately following the plasma conditioning releases Cs to provide coverage on the ion conversion surfaces. The effectiveness of the ion source conditioning and cesiation is monitored with plasma emission spectroscopy using a high-sensitivity optical spectrometer. Plasma emission spectroscopy is also used to provide a mean for diagnosing and confirming a failure of the insulating coating of the ion source RF antenna which is immersed in the plasma. Emissions of composition elements of the antenna coating material, Na emission being the most significant, drastically elevate to signal a failure when it happens. Plasma spectra of the developmental ion source with an AlN chamber and an external RF antenna are also briefly discussed.

  19. Webinar Presentation: Characterization of Emissions from Small, Variable Solid Fuel Combustion Sources for Determining Global Emissions and Climate Impact

    EPA Pesticide Factsheets

    This presentation, Characterization of Emissions from Small, Variable Solid Fuel Combustion Sources for Determining Global Emissions and Climate Impact, was given at the STAR Black Carbon 2016 Webinar Series.

  20. Microwave subsecond pulses in solar flares - source localization, emission mechanism

    NASA Astrophysics Data System (ADS)

    Altyntsev, A. T.; Kardapolova, N. N.; Kuznetsov, A. A.; Lesovoi, S. V.; Meshalkina, N. S.; Yan, Y.

    The observations of bursts with fine temporal structures is one of few ways to study the primary energy release sites in solar flares. The localization of their sources in a flare region using the Siberian Solar Radio Telescope data (5.7 GHz) provide us with the unique possibility to determine plasma parameters, and to verify emission mechanisms. The simultaneous spectral observations (5.2 - 7.7 GHz) were provided by National Astronomical Observatories/Beijing spectropolarimeters. An analysis is made of the subsecond pulses of different types: short duration wide band pulses, U-type cm-bursts, the bursts with the "zebra" pattern. The suggestion is justified that in many cases the frequency drifts are response to the plasma density dynamics in the local sites in flare loops. It is argued that the conditions of emission escaping from the source strongly influent the apparent source sizes and the polarization degree of the subsecond sources. This research was supported by Grants 02-02-39030 and 03-02-16229 of RFBR, and E02-3.2-489 of Education department of Russia.

  1. Plasmonic nanogaps for broadband and large spontaneous emission rate enhancement

    SciTech Connect

    Edwards, Anthony P.; Adawi, Ali M.

    2014-02-07

    We present the optical properties of a plasmonic nanogap formed between a silver metallic nanoparticle and an extended silver film that shows a strong enhancement in the spontaneous emission rate over the whole visible range. In particular, we use three-dimensional finite difference time domain calculations to study the spontaneous emission rate and the quantum efficiency of an emitting material placed within the gap region as a function of the geometrical parameters of the plasmonic nanogap. Our calculations reveal that the enhancements in the total decay rate can be divided into two regions as a function of wavelength; region I spans the wavelength range from 350 nm to 500 nm and peaks at approximately at 400 nm. Region II covers the spectral range between 500 nm and 1000 nm. The enhancements in total decay rate in region I are mainly dominated by Ohmic losses by the metal, while the enhancements in total decay rate in region II are mainly dominated by radiative decay rate enhancements. Furthermore, our calculations show over 100 times enhancement in the spontaneous emission rate in region II. We combine this with quantum efficiency enhancements of almost 30 times from materials with low intrinsic quantum efficiencies and only a small reduction in efficiency from those with high intrinsic quantum efficiencies. All results appear easily achievable using realistic geometrical parameters and simple synthesis techniques. These results are attributed to the strong field confinements in the nanogap region. The structures are of high interest for both the fundamental understanding of light mater interactions under extreme electromagnetic field confinements and also potential applications in quantum optics and Raman spectroscopy.

  2. Measurement of roadway PM10 emission rates using tracer techniques. Final technical report

    SciTech Connect

    Kantamaneni, R.; Claiborn, C.

    1996-03-01

    In the work, stationary and mobile point source tracer release techniques were used to determine PM10 emission rates from 4-lane commercia/residential paved roads under sanded and unsanded conditions, and from unpaved roads relative to site specific vehicular and ambient parameters. Measured stress (4+ lanes; > or = to 10,000 vehicles/day) emission factors for unsanded and sanded roads were respectively 40% and 10% lower than the EPA approved reference value. Preliminary results indicate a consistent relationship between PM10 and relative humidity under unsanded conditions. Evidence suggests that street sweeping has a negligible effect on PM10 emission reduction. Considerable uncertainties were observed with the empirical emission factor equation.

  3. Air quality assessment and control of emission rates.

    PubMed

    Skiba, Yuri N; Parra-Guevara, David; Belitskaya, Davydova Valentina

    2005-12-01

    Mathematical methods based on the adjoint model approach are given for the air-pollution estimation and control in an urban region. A simple advection-diffusion-reaction model and its adjoint are used to illustrate the application of the methods. Dual pollution concentration estimates in ecologically important zones are derived and used to develop two non-optimal strategies and one optimal strategy for controlling the emission rates of enterprises. A linear convex combination of these strategies represents a new sufficient strategy. A method for detecting the enterprises, which violate the emission rates prescribed by a control, is given. A method for determining an optimal position for a new enterprise in the region is also described.

  4. Updated emission inventories for speciated atmospheric mercury from anthropogenic sources in China.

    PubMed

    Zhang, Lei; Wang, Shuxiao; Wang, Long; Wu, Ye; Duan, Lei; Wu, Qingru; Wang, Fengyang; Yang, Mei; Yang, Hai; Hao, Jiming; Liu, Xiang

    2015-03-03

    China is the largest contributor to global atmospheric mercury (Hg), and accurate emission inventories in China are needed to reduce large gaps existing in global Hg mass balance estimates and assess Hg effects on various ecosystems. The China Atmospheric Mercury Emission (CAME) model was developed in this study using probabilistic emission factors generated from abundant on-site measurements and literature data. Using this model, total anthropogenic Hg emissions were estimated to be continuously increasing from 356 t in 2000 to 538 t in 2010 with an average annual increase rate of 4.2%. Industrial coal combustion, coal-fired power plants, nonferrous metal smelting, and cement production were identified to be the dominant Hg emission sources in China. The ten largest contributing provinces accounted for nearly 60% of the total Hg emissions in 2010. Speciated Hg emission inventory was developed over China with a grid-resolution of 36 × 36 km, providing needed emission fields for Hg transport models. In this new inventory, the sectoral Hg speciation profiles were significantly improved based on the latest data from field measurements and more detailed technology categorization. The overall uncertainties of the newly developed inventory were estimated to be in the range of -20% to +23%.

  5. Field measurement of greenhouse gas emission rates and development of emission factors for wastewater treatment. Final report, September 1994-March 1997

    SciTech Connect

    Eklund, B.; LaCosse, J.

    1997-09-01

    The report gives results of field testing to develop more reliable greenhouse gas (GHG) emission estimates for Wastewater treatment (WWT) lagoons. Field tests of emissions were conducted for WWT lagoons that use anaerobic processes to treat large volumes of wastewater with large biological oxygen demand (BOD) loadings. Air emissions and wastewater were measured at anaerobic lagoons at three meat processing plants and two publicly owned treatment works. The overall emission rates of CH4, carbon dioxide, carbon monoxide, nitrous oxide, ammonia (NH3), and chlorofluorocarbons were measured from each source using an open-path monitoring approach. The emitted compounds were identified and quantified by Fourier-Transform Infrared spectroscopy. Emission factors were developed for CH4 and NH3 as a function of the plant production rate, wastewater parameters (e.g., influent BOD and chemical oxygen demand (COD) loadings), and WWT system performance (e.g., BOD and COD removal rates).

  6. Application of optical emission spectroscopy to high current proton sources

    NASA Astrophysics Data System (ADS)

    Castro, G.; Mazzaglia, M.; Nicolosi, D.; Mascali, D.; Reitano, R.; Zaniol, B.; Celona, L.; Leonardi, O.; Leone, F.; Naselli, E.; Neri, L.; Torrisi, G.; Gammino, S.

    2017-07-01

    Optical Emission Spectroscopy (OES) represents a very reliable technique to carry out non-invasive measurements of plasma density and plasma temperature in the range of tens of eV. With respect to other diagnostics, it also can characterize the different populations of neutrals and ionized particles constituting the plasma. At INFN-LNS, OES techniques have been developed and applied to characterize the plasma generated by the Flexible Plasma Trap, an ion source used as "testbench" of the proton source built for European Spallation Source. This work presents the characterization of the parameters of a hydrogen plasma in different conditions of neutral pressure, microwave power and magnetic field profile, along with perspectives for further upgrades of the OES diagnostics system.

  7. Volatile organic compound emission rates from mixed deciduous and coniferous forests in Northern Wisconsin, USA

    NASA Astrophysics Data System (ADS)

    Isebrands, J. G.; Guenther, A. B.; Harley, P.; Helmig, D.; Klinger, L.; Vierling, L.; Zimmerman, P.; Geron, C.

    Biogenic emissions of volatile organic compounds (VOC) from forests play an important role in regulating the atmospheric trace gas composition including global tropospheric ozone concentrations. However, more information is needed on VOC emission rates from different forest regions of the world to understand regional and global impacts and to implement possible mitigation strategies. The mixed deciduous and coniferous forests of northern Wisconsin, USA, were predicted to have significant VOC emission rates because they are comprised of many genera (i.e. Picea, Populus, Quercus, Salix) known to be high VOC emitters. In July 1993, a study was conducted on the Chequamegon National Forest near Rhinelander, WI, to identify and quantify VOC emitted from major trees, shrubs, and understory herbs in the mixed northern forests of this region. Emission rates were measured at various scales - at the leaf level with cuvettes, the branch level with branch enclosures, the canopy level with a tower based system, and the landscape level with a tethered balloon air sampling system. Area-average emission rates were estimated by scaling, using biomass densities and species composition along transects representative of the study site. Isoprene (C 5H 8) was the primary VOC emitted, although significant quantities of monoterpenes (C 10H 16) were also emitted. The highest emission rates of isoprene (at 30°C and photosynthetically active radiation of 1000 μmol m -2 s -1) were from northern red oak ( Quercus rubra, >110 μg(C) g -1 h -1); aspen ( Populus tremuloides, >77); willow ( Salix spp., >54); and black spruce ( Picea mariana, >10). Emission rates of hybrid poplar clones ranged from 40 to 90 μg(C) g -1 h -1 at 25°C; those of Picea provenances were generally <10, and emission rates of a hybrid between North American and European spruces were intermediate to parental rates. More than 30 species of plants were surveyed from the sites, including several from previously unstudied

  8. The Sources of F10.7 Emission

    NASA Astrophysics Data System (ADS)

    Schonfeld, S.; White, S. M.; Henney, C. J.; Mcateer, R.; Arge, C. N.

    2013-12-01

    The solar radio flux at a wavelength of 10.7 cm, F10.7, serves as a proxy for the Sun's ionizing flux striking the Earth and is a heavily used index for space weather studies. In principle both the coronal sources of ionizing flux and strong coronal magnetic fields contribute to F10.7 via different emission mechanisms. Recently the Expanded Very Large Array (EVLA) has added the capability to make high-spatial-resolution images of the Sun at 10.7 cm. In this work we compare a trial F10.7 image from the EVLA with the radio emission predicted to be present from EUV images of the Sun acquired by the AIA telescope on the Solar Dynamics Observatory at 6 wavelengths covering the coronal temperature range. Photospheric magnetograms are used to identify likely regions of strong coronal magnetic field, and the circular polarization measured by the EVLA is used as a tracer of gyroresonance contributions to F10.7. We discuss the conversion of the EUV data to bremsstrahlung radio fluxes via the construction of differential emission measure images, and analyze the relative contributions of the different sources of F10.7 flux.

  9. The Sources of F10.7 Emission

    NASA Astrophysics Data System (ADS)

    Schonfeld, Samuel J.; White, Stephen M.; Henney, Carl John; McAteer, James; Arge, Charles

    2014-06-01

    The solar radio flux at a wavelength of 10.7 cm, F10.7, serves as a proxy for the Sun’s ionizing flux striking the Earth and is a heavily used index for space weather studies. In principal both the coronal sources of ionizing flux and strong coronal magnetic fields contribute to F10.7 via different emission mechanisms. Recently the Expanded Very Large Array (EVLA) has added the capability to make high-spatial-resolution images of the Sun at 10.7 cm. In this work we compare a trial F10.7 image from the EVLA with the radio emission predicted to be present from EUV images of the Sun acquired by the AIA telescope on the Solar Dynamics Observatory at 6 wavelengths covering the coronal temperature range. Photospheric magnetograms are used to identify likely regions of strong coronal magnetic field, and the circular polarization measured by the EVLA is used as a tracer of gyroresonance contributions to F10.7. We discuss the conversion of the EUV data to bremsstrahlung radio fluxes via the construction of differential emission measure images, and analyze the relative contributions of the different sources of F10.7 flux.

  10. Scenarios of global mercury emissions from anthropogenic sources

    NASA Astrophysics Data System (ADS)

    Rafaj, P.; Bertok, I.; Cofala, J.; Schöpp, W.

    2013-11-01

    This paper discusses the impact of air quality and climate policies on global mercury emissions in the time horizon up to 2050. Evolution of mercury emissions is based on projections of energy consumption for a scenario without any global greenhouse gas mitigation efforts, and for a 2 °C climate policy scenario, which assumes internationally coordinated action to mitigate climate change. The assessment takes into account current air quality legislation in each country, as well as provides estimates of maximum feasible reductions in mercury through 2050. Results indicate significant scope for co-benefits of climate policies for mercury emissions. Atmospheric releases of mercury from anthropogenic sources under the global climate mitigation regime are reduced in 2050 by 45% when compared to the case without climate measures. Around one third of world-wide co-benefits for mercury emissions by 2050 occur in China. An annual Hg-abatement of about 800 tons is estimated for the coal combustion in power sector if the current air pollution legislation and climate policies are adopted in parallel.

  11. Real-world volatile organic compound emission rates from seated adults and children for use in indoor air studies.

    PubMed

    Stönner, C; Edtbauer, A; Williams, J

    2017-07-06

    Human beings emit many volatile organic compounds (VOCs) of both endogenous (internally produced) and exogenous (external source) origin. Here we present real-world emission rates of volatile organic compounds from cinema audiences (50-230 people) as a function of time in multiple screenings of three films. The cinema location and film selection allowed high-frequency measurement of human-emitted VOCs within a room flushed at a known rate so that emissions rates could be calculated for both adults and children. Gas-phase emission rates are analyzed as a function of time of day, variability during the film, and age of viewer. The average emission rates of CO2 , acetone, and isoprene were lower (by a factor of ~1.2-1.4) for children under twelve compared to adults while for acetaldehyde emission rates were equivalent. Molecules influenced by exogenous sources such as decamethylcyclopentasiloxanes and methanol tended to decrease over the course of day and then rise for late evening screenings. These results represent average emission rates of people under real-world conditions and can be used in indoor air quality assessments and building design. Averaging over a large number of people generates emission rates that are less susceptible to individual behaviors. © 2017 The Authors. Indoor Air published by John Wiley & Sons Ltd.

  12. A fast source for quantitative acoustic emission and its application

    NASA Astrophysics Data System (ADS)

    Masaki, Ryuji; Takemoto, Mikio; Ono, Kanji

    1999-12-01

    We demonstrate a new artificial fracture source for quantitative acoustic emission (AE) characterization. The source utilizes the break-down of silicone oil (or other liquids) placed inside a crack (or a slit). This is a dipole source with a rise time under 0.1 μs. It is much faster than a pencil-lead-break source and allows the calibration of a sensor-structure system to 7-10 MHz. We irradiated a focused Q-switched Nd-YAG laser beam (15 to 90 mJ energy) on silicon placed in a slit on a cylindrical block. The out-of-plane displacement produced by the resultant bulk waves was monitored on the outside surface using a heterodyne-type laser interferometer. This break-down source was employed to determine the transfer functions of an AE transducer and propagation medium. Finally, we studied AE signals due to the delayed fracture of a butt-welded dual-phase stainless steel, using the break-down source for calibration. Brittle-fracture events were successfully characterized.

  13. 76 FR 15371 - Standards of Performance for New Stationary Sources and Emission Guidelines for Existing Sources...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-21

    ...This action promulgates EPA's new source performance standards and emission guidelines for sewage sludge incineration units located at wastewater treatment facilities designed to treat domestic sewage sludge. This final rule sets limits for nine pollutants under section 129 of the Clean Air Act: Cadmium, carbon monoxide, hydrogen chloride, lead, mercury, nitrogen oxides, particulate matter,......

  14. 76 FR 15703 - Standards of Performance for New Stationary Sources and Emission Guidelines for Existing Sources...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-21

    ...This action promulgates EPA's final response to the 2001 voluntary remand of the December 1, 2000, new source performance standards and emission guidelines for commercial and industrial solid waste incineration units and the vacatur and remand of several definitions by the District of Columbia Circuit Court of Appeals in 2007. In addition, this action includes the 5-year technology review of......

  15. 76 FR 18407 - Standards of Performance for New Stationary Sources and Emissions Guidelines for Existing Sources...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-04-04

    ... AGENCY 40 CFR Part 60 RIN 2060-AQ24 Standards of Performance for New Stationary Sources and Emissions... Populations K. Congressional Review Act A red-line version of the regulatory language that incorporates the... 40 CFR 60.50c of subpart Ec. If you have any questions regarding the applicability of the...

  16. Current Methodologies in Preparing Mobile Source Port-Related Emission Inventories Final Report April 2009

    EPA Pesticide Factsheets

    This report focuses on mobile emission sources at ports, including oceangoing vessels (OGVs), harbor craft, and cargo handling equipment (CHE), as well as other land-side mobile emission sources at ports, such as locomotives and on-highway vehicles.

  17. REVISED EMISSIONS ESTIMATION METHODOLOGIES FOR INDUSTRIAL, RESIDENTIAL, AND ELECTRIC UTILITY STATIONARY COMBUSTION SOURCES

    EPA Science Inventory

    The report describes the development of improved and streamlined EPA emission estimation methods for stationary combustion area sources by the Joint Emissions Inventory Oversight Group (JEIOG) research program. These sources include categories traditionally labeled "other statio...

  18. REVISED EMISSIONS ESTIMATION METHODOLOGIES FOR INDUSTRIAL, RESIDENTIAL, AND ELECTRIC UTILITY STATIONARY COMBUSTION SOURCES

    EPA Science Inventory

    The report describes the development of improved and streamlined EPA emission estimation methods for stationary combustion area sources by the Joint Emissions Inventory Oversight Group (JEIOG) research program. These sources include categories traditionally labeled "other statio...

  19. 40 CFR 63.1356 - Sources with multiple emission limits or monitoring requirements.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... POLLUTANTS FOR SOURCE CATEGORIES National Emission Standards for Hazardous Air Pollutants From the Portland Cement Manufacturing Industry Other § 63.1356 Sources with multiple emission limits or monitoring...

  20. 40 CFR 63.1356 - Sources with multiple emission limits or monitoring requirements.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... POLLUTANTS FOR SOURCE CATEGORIES National Emission Standards for Hazardous Air Pollutants From the Portland Cement Manufacturing Industry Other § 63.1356 Sources with multiple emission limits or monitoring...

  1. A framework for emissions source apportionment in industrial areas: MM5/CALPUFF in a near-field application.

    PubMed

    Ghannam, K; El-Fadel, M

    2013-02-01

    This paper examines the relative source contribution to ground-level concentrations of carbon monoxide (CO), nitrogen dioxide (NO2), and PM10 (particulate matter with an aerodynamic diameter < 10 microm) in a coastal urban area due to emissions from an industrial complex with multiple stacks, quarrying activities, and a nearby highway. For this purpose, an inventory of CO, oxide of nitrogen (NO(x)), and PM10 emissions was coupled with the non-steady-state Mesoscale Model 5/California Puff Dispersion Modeling system to simulate individual source contributions under several spatial and temporal scales. As the contribution of a particular source to ground-level concentrations can be evaluated by simulating this single-source emissions or otherwise total emissions except that source, a set of emission sensitivity simulations was designed to examine if CALPUFF maintains a linear relationship between emission rates and predicted concentrations in cases where emitted plumes overlap and chemical transformations are simulated. Source apportionment revealed that ground-level releases (i.e., highway and quarries) extended over large areas dominated the contribution to exposure levels over elevated point sources, despite the fact that cumulative emissions from point sources are higher. Sensitivity analysis indicated that chemical transformations of NO(x) are insignificant, possibly due to short-range plume transport, with CALPUFF exhibiting a linear response to changes in emission rate. The current paper points to the significance of ground-level emissions in contributing to urban air pollution exposure and questions the viability of the prevailing paradigm of point-source emission reduction, especially that the incremental improvement in air quality associated with this common abatement strategy may not accomplish the desirable benefit in terms of lower exposure with costly emissions capping. The application of atmospheric dispersion models for source apportionment helps in

  2. A new approach to estimation of methane emission rates from landfills.

    PubMed

    Zhu, Han; Letzel, Marcus O; Reiser, Martin; Kranert, Martin; Bächlin, Wolfgang; Flassak, Thomas

    2013-12-01

    Methane emission monitoring has become increasingly essential for diffusive area sources, especially for landfills, which contribute to a significant fraction of the total anthropogenic methane emission globally. Statutorily, methane emission rate from landfills in Germany shall be examined on a semiannual basis; however, an appropriate approach has yet to be developed and adopted for general use. In this study, a new method is proposed based on experimental results, which utilizes a TDLAS (Tunable Diode Laser Absorption Spectroscopy) instrument - GasFinder2.0 system and a dispersion model LASAT (Lagrangian Simulation of Aerosol Transport) as the measurement device and calculation model, respectively. Between April 2010 and December 2011, a research project was conducted at a pilot scale landfill in the south of Germany. Drawing on the extensive research into this pilot project, an effective strategy of measurement setup was determined. Methane concentration was measured with GasFinder2.0 system in the upstream and downstream sections of the project site, while wind and turbulence data were measured simultaneously by an ultrasonic anemometer. The average methane emission rate from the source can be calculated by using the results as input data in the dispersion model. With this method, site-specific measurement approaches can be designed for not only landfills, but also different diffusive area sources with less workload and lower cost compared to conventional FID (Flame Ionization Detector) method. Copyright © 2013 Elsevier Ltd. All rights reserved.

  3. 75 FR 42676 - National Emission Standards for Hazardous Air Pollutants for Major Sources: Industrial...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-07-22

    ... Pollutants for Major Sources: Industrial, Commercial, and Institutional Boilers and Process Heaters; National... Boilers; Standards of Performance for New Stationary Sources and Emission Guidelines for Existing Sources... Boilers and Process Heaters located at major sources; Industrial, Commercial, and Institutional...

  4. Noise source emissions, Deaf Smith County site, Texas

    SciTech Connect

    Not Available

    1987-05-13

    Noise source data and use factors for modeling the noise environment expected from salt site repository activity were provided by Battelle Columbus Division. This report has been prepared for the purpose of documenting the development of the data provided to the Repository Project Management (RPM) organization. The data provided encompass all phases of activity from site preparation through construction of the exploratory shaft facility (ESF). Noise environments expected from construction and operation of transportation corridors associated with the activity were also modeled. The equipment inventory, including sound-power levels for each item, is included. Emission source terms provided by Parsons Brinckerhoff/PB-KBB for the ESF were used as a basis for the noise-source emission inventory development. Where available, research results containing complete spectra were used. In cases where complete data were not available, a sound-pressure spectrum was synthesized from a characteristic spectrum shape from a similar piece of equipment. For example, a front-shovel excavator might be approximated by data from a front-end loader of similar horsepower range. Sound-power-level spectra were then calculated from the sound-pressure-level data. 2 refs.

  5. Soil organic carbon dust emission: an omitted global source of atmospheric CO2.

    PubMed

    Chappell, Adrian; Webb, Nicholas P; Butler, Harry J; Strong, Craig L; McTainsh, Grant H; Leys, John F; Viscarra Rossel, Raphael A

    2013-10-01

    Soil erosion redistributes soil organic carbon (SOC) within terrestrial ecosystems, to the atmosphere and oceans. Dust export is an essential component of the carbon (C) and carbon dioxide (CO(2)) budget because wind erosion contributes to the C cycle by removing selectively SOC from vast areas and transporting C dust quickly offshore; augmenting the net loss of C from terrestrial systems. However, the contribution of wind erosion to rates of C release and sequestration is poorly understood. Here, we describe how SOC dust emission is omitted from national C accounting, is an underestimated source of CO(2) and may accelerate SOC decomposition. Similarly, long dust residence times in the unshielded atmospheric environment may considerably increase CO(2) emission. We developed a first approximation to SOC enrichment for a well-established dust emission model and quantified SOC dust emission for Australia (5.83 Tg CO(2)-e yr(-1)) and Australian agricultural soils (0.4 Tg CO(2)-e yr(-1)). These amount to underestimates for CO(2) emissions of ≈10% from combined C pools in Australia (year = 2000), ≈5% from Australian Rangelands and ≈3% of Australian Agricultural Soils by Kyoto Accounting. Northern hemisphere countries with greater dust emission than Australia are also likely to have much larger SOC dust emission. Therefore, omission of SOC dust emission likely represents a considerable underestimate from those nations' C accounts. We suggest that the omission of SOC dust emission from C cycling and C accounting is a significant global source of uncertainty. Tracing the fate of wind-eroded SOC in the dust cycle is therefore essential to quantify the release of CO(2) from SOC dust to the atmosphere and the contribution of SOC deposition to downwind C sinks. © 2013 John Wiley & Sons Ltd.

  6. Biosolid stockpiles are a significant point source for greenhouse gas emissions.

    PubMed

    Majumder, Ramaprasad; Livesley, Stephen J; Gregory, David; Arndt, Stefan K

    2014-10-01

    The wastewater treatment process generates large amounts of sewage sludge that are dried and then often stored in biosolid stockpiles in treatment plants. Because the biosolids are rich in decomposable organic matter they could be a significant source for greenhouse gas (GHG) emissions, yet there are no direct measurements of GHG from stockpiles. We therefore measured the direct emissions of methane (CH4), nitrous oxide (N2O) and carbon dioxide (CO2) on a monthly basis from three different age classes of biosolid stockpiles at the Western Treatment Plant (WTP), Melbourne, Australia, from December 2009 to November 2011 using manual static chambers. All biosolid stockpiles were a significant point source for CH4 and N2O emissions. The youngest biosolids (<1 year old) had the greatest CH4 and N2O emissions of 60.2 kg of CO2-e per Mg of biosolid per year. Stockpiles that were between 1 and 3 years old emitted less overall GHG (∼29 kg CO2-e Mg(-1) yr(-1)) and the oldest stockpiles emitted the least GHG (∼10 kg CO2-e Mg(-1) yr(-1)). Methane emissions were negligible in all stockpiles but the relative contribution of N2O and CO2 changed with stockpile age. The youngest stockpile emitted two thirds of the GHG emission as N2O, while the 1-3 year old stockpile emitted an equal amount of N2O and CO2 and in the oldest stockpile CO2 emissions dominated. We did not detect any seasonal variability of GHG emissions and did not observe a correlation between GHG flux and environmental variables such as biosolid temperature, moisture content or nitrate and ammonium concentration. We also modeled CH4 emissions based on a first order decay model and the model based estimated annual CH4 emissions were higher as compared to the direct field based estimated annual CH4 emissions. Our results indicate that labile organic material in stockpiles is decomposed over time and that nitrogen decomposition processes lead to significant N2O emissions. Carbon decomposition favors CO2 over

  7. Mapping Fugitive Gas Emission Sources and Severity Across Southeastern Saskatchewan

    NASA Astrophysics Data System (ADS)

    Baillie, J.; Risk, D. A.; Lavoie, M.; Williams, J. P.

    2015-12-01

    Southeastern Saskatchewan, Canada contains a 10,000 km2 region heavily developed by oil and gas activity that has been struggling with air quality issues, arising from hundreds or thousands of oil and gas leak points. The region is also very diverse in terms of oilfield operators, who use extraction techniques including conventional, enhanced oil recovery (EOR), and fracking. As regulators and operators need more knowledge about emission patterns locally, we undertook comprehensive mapping and characterization of leak sources at the regional scale using vehicle-based data collection, together with computational techniques. We measured the presence and source of fugitive emissions from infrastructure and oilfield activities in eight 100 km2 survey domains. These included two controls with no oil and gas activity, and otherwise the domains were selected to capture the diversity of development; targeting primarily conventional and EOR activities in the Weyburn-Midale beds, and unconventional activities in the Bakken play. A total of 25 unique operators fell within the survey domains. Each domain was surveyed multiple times for CO2, CH4, and H2S, allowing us to identify persistent leaks and to screen out one-time events. The multiple gas targets also provided opportunities for discriminating one type of fugitive emission from another (i.e. flares from storage tanks) using ratios of excess (above ambient) concentrations, after correcting for natural background variability with a signal-processing routine. Fugitive emissions were commonly observed in all study domains. Most emissions were associated with oil and gas infrastructure, as opposed to drilling and other short-term activities. There were obvious emissions at many well pads, storage tanks, and flares. We also observed high geochemical variability around flares, with some being very effective in combusting toxic gases, and others less so. Almost all observed concentrations fell below regulatory limits, but have a

  8. Technologies and policies for "hard to scrub" emissions sources

    NASA Astrophysics Data System (ADS)

    Friedmann, J.

    2016-12-01

    The science of climate change yields harsh math regarding atmospheric accumulations of GHGs. The world is far from target trajectories for 2C or 1.5C, and the global carbon budget is severe. To achieve those targets requires two things. First, we must field technologies that reduce emissions from the "hard to scrub" parts of the US and global economies, such as heavy industry (cement and steel), aviation, ocean shipping, and household cooking and heating. Second, we will likely need negative emissions pathways for those sources that prove extremely difficult to remove or reduce - the climate equivalent of adding revenue to one's budget. Such pathways may well need to convert GHG emissions (especially CO2 and methane) into useful products with minimal infrastructure builds. Dramatic advances in advanced manufacturing, 3D printing, simulation, modeling, and data analytics have made possible solutions which were previously unthinkable or impossible. This include "bespoke reactors", which can simultaneously perform separations and conversions; low-cost modular chemical systems of any scale; biologically inspired or biologically mediated energy services; direct air carbon-capture systems; and electrochemical pathways for emissions reduction and conversion. However, these approaches are unlikely to be fielded without policy actions or reforms that support such systems in competitive global energy markets. Such policy measures do NOT require a carbon price. Rather, they could include individual or combined measures such as emission or performance standards, financial incentives (like tax credits or low-cost access to capital), border adjustable tariffs, creation of CO2 utilities, ands public good surcharges. Innovation in both technical and policy arenas are needed to achieve the goals of the Paris agreement signatories, and these innovations can be simultaneously configured to deliver substantive greenhouse gas mitigation.

  9. 40 CFR 63.5984 - What emission limits must I meet for tire production affected sources?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... tire production affected sources? 63.5984 Section 63.5984 Protection of Environment ENVIRONMENTAL...: Rubber Tire Manufacturing Emission Limits for Tire Production Affected Sources § 63.5984 What emission limits must I meet for tire production affected sources? You must meet each emission limit in either...

  10. 40 CFR 63.5984 - What emission limits must I meet for tire production affected sources?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... tire production affected sources? 63.5984 Section 63.5984 Protection of Environment ENVIRONMENTAL...: Rubber Tire Manufacturing Emission Limits for Tire Production Affected Sources § 63.5984 What emission limits must I meet for tire production affected sources? You must meet each emission limit in either...

  11. 40 CFR 63.5984 - What emission limits must I meet for tire production affected sources?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... tire production affected sources? 63.5984 Section 63.5984 Protection of Environment ENVIRONMENTAL... POLLUTANTS FOR SOURCE CATEGORIES National Emissions Standards for Hazardous Air Pollutants: Rubber Tire Manufacturing Emission Limits for Tire Production Affected Sources § 63.5984 What emission limits must I meet...

  12. 40 CFR 63.5984 - What emission limits must I meet for tire production affected sources?

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... tire production affected sources? 63.5984 Section 63.5984 Protection of Environment ENVIRONMENTAL...: Rubber Tire Manufacturing Emission Limits for Tire Production Affected Sources § 63.5984 What emission limits must I meet for tire production affected sources? You must meet each emission limit in either...

  13. 40 CFR 63.5984 - What emission limits must I meet for tire production affected sources?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... tire production affected sources? 63.5984 Section 63.5984 Protection of Environment ENVIRONMENTAL... POLLUTANTS FOR SOURCE CATEGORIES National Emissions Standards for Hazardous Air Pollutants: Rubber Tire Manufacturing Emission Limits for Tire Production Affected Sources § 63.5984 What emission limits must I meet...

  14. Sulfur Dioxide Emission Rates from Kilauea Volcano, Hawai`i, an Update: 2002-2006

    USGS Publications Warehouse

    Elias, Tamar; Sutton, A.J.

    2007-01-01

    Introduction Sulfur dioxide (SO2) emission rates from Kilauea Volcano were first measured by Stoiber and Malone (1975) and have been measured on a regular basis since 1979 (Greenland and others, 1985; Casadevall and others, 1987; Elias and others, 1998; Sutton and others, 2001, Elias and Sutton, 2002, Sutton and others, 2003). Compilations of SO2 emission-rate and wind-vector data from 1979 through 2001 are available on the web. (Elias and others, 1998 and 2002). This report updates the database through 2006, and documents the changes in data collection and processing that have occurred during the interval 2002-2006. During the period covered by this report, Kilauea continued to release SO2 gas predominantly from its summit caldera and east rift zone (ERZ) (Elias and others, 1998; Sutton and others, 2001, Elias and others, 2002, Sutton and others, 2003). These two distinct sources are always measured independently (fig.1). Sulphur Banks is a minor source of SO2 and does not contribute significantly to the total emissions for Kilauea (Stoiber and Malone, 1975). From 1979 until 2003, summit and east rift zone emission rates were derived using vehicle- and tripod- based Correlation Spectrometry (COSPEC) measurements. In late 2003, we began to augment traditional COSPEC measurements with data from one of the new generation of miniature spectrometer systems, the FLYSPEC (Horton and others, 2006; Elias and others, 2006, Williams-Jones and others, 2006).

  15. Urban sources and emissions of nitrous oxide and methane in southern California, USA

    NASA Astrophysics Data System (ADS)

    Townsend-Small, A.; Pataki, D.; Tyler, S. C.; Czimczik, C. I.; Xu, X.; Christensen, L. E.

    2012-12-01

    Anthropogenic activities have resulted in increasing levels of greenhouse gases, including carbon dioxide, methane, and nitrous oxide. While global and regional emissions sources of carbon dioxide are relatively well understood, methane and nitrous oxide are less constrained, particularly at regional scales. Here we present the results of an investigation of sources and emissions of methane and nitrous oxide in Los Angeles, California, USA, one of Earth's largest urban areas. The original goal of the project was to determine whether isotopes are useful tracers of agricultural versus urban nitrous oxide and methane sources. For methane, we found that stable isotopes (carbon-13 and deuterium) and radiocarbon are good tracers of biogenic versus fossil fuel sources. High altitude observations of methane concentration, measured continuously using tunable laser spectroscopy, and isotope ratios, measured on discrete flask samples using mass spectrometry, indicate that the predominant methane source in Los Angeles is from fossil fuels, likely from "fugitive" emissions from geologic formations, natural gas pipelines, oil refining, or power plants. We also measured nitrous oxide emissions and isotope ratios from urban (landscaping and wastewater treatment) and agricultural sources (corn and vegetable fields). There was no difference in nitrous oxide isotope ratios between the different types of sources, although stable isotopes did differ between nitrous oxide produced in oxic and anoxic wastewater treatment tanks. Our nitrous oxide flux data indicate that landscaped turfgrass emits nitrous oxide at rates equivalent to agricultural systems, indicating that ornamental soils should not be disregarded in regional nitrous oxide budgets. However, we also showed that wastewater treatment is a much greater source of nitrous oxide than soils regionally. This work shows that global nitrous oxide and methane budgets are not easily downscaled to regional, urban settings, which has

  16. Evaluating measurements of carbon dioxide emissions using a precision source--A natural gas burner.

    PubMed

    Bryant, Rodney; Bundy, Matthew; Zong, Ruowen

    2015-07-01

    A natural gas burner has been used as a precise and accurate source for generating large quantities of carbon dioxide (CO2) to evaluate emissions measurements at near-industrial scale. Two methods for determining carbon dioxide emissions from stationary sources are considered here: predicting emissions based on fuel consumption measurements-predicted emissions measurements, and direct measurement of emissions quantities in the flue gas-direct emissions measurements. Uncertainty for the predicted emissions measurement was estimated at less than 1%. Uncertainty estimates for the direct emissions measurement of carbon dioxide were on the order of ±4%. The relative difference between the direct emissions measurements and the predicted emissions measurements was within the range of the measurement uncertainty, therefore demonstrating good agreement. The study demonstrates how independent methods are used to validate source emissions measurements, while also demonstrating how a fire research facility can be used as a precision test-bed to evaluate and improve carbon dioxide emissions measurements from stationary sources. Fossil-fuel-consuming stationary sources such as electric power plants and industrial facilities account for more than half of the CO2 emissions in the United States. Therefore, accurate emissions measurements from these sources are critical for evaluating efforts to reduce greenhouse gas emissions. This study demonstrates how a surrogate for a stationary source, a fire research facility, can be used to evaluate the accuracy of measurements of CO2 emissions.

  17. Quantification of methane emission rates from coal mine ventilation shafts using airborne remote sensing data

    NASA Astrophysics Data System (ADS)

    Krings, T.; Gerilowski, K.; Buchwitz, M.; Hartmann, J.; Sachs, T.; Erzinger, J.; Burrows, J. P.; Bovensmann, H.

    2012-10-01

    The quantification of emissions of the greenhouse gas methane is essential for attributing the roles of anthropogenic activity and natural phenomena in global climate change. Our current measurement systems and networks whilst having improved during the last decades, are deficient in many respects. For example, the emissions from localised and point sources such as landfills or fossil fuel exploration sites are not readily assessed. A tool developed to better understand point sources of the greenhouse gases carbon dioxide and methane is the optical remote sensing instrument MAMAP, operated from aircraft. After a recent instrument modification, retrievals of the column averaged dry air mole fractions for methane XCH4 (or for carbon dioxide XCO2) derived from MAMAP data, have a precision of about 0.4% or better and thus can be used to infer emission rate estimates using an optimal estimation inverse Gaussian plume model or a simple integral approach. CH4 emissions from two coal mine ventilation shafts in Western Germany surveyed during the AIRMETH 2011 measurement campaign are used as examples to demonstrate and assess the value of MAMAP data for quantifying CH4 from point sources. While the knowledge of the wind is an important input parameter in the retrieval of emissions from point sources and is generally extracted from models, additional information from a turbulence probe operated on-board the same aircraft was utilised to enhance the quality of the emission estimates. Although flight patterns were optimised for remote sensing measurements, data from an in-situ analyser for CH4 were found to be in good agreement with retrieved dry columns of CH4 from MAMAP and could be used to investigate and refine underlying assumptions for the inversion procedures. With respect to the total emissions of the mine at the time of the overflight, the inferred emission rate of 50.4 kt CH4 yr-1 has a difference of less than 1% compared to officially reported values by the mine

  18. Quantification of methane emission rates from coal mine ventilation shafts using airborne remote sensing data

    NASA Astrophysics Data System (ADS)

    Krings, T.; Gerilowski, K.; Buchwitz, M.; Hartmann, J.; Sachs, T.; Erzinger, J.; Burrows, J. P.; Bovensmann, H.

    2013-01-01

    The quantification of emissions of the greenhouse gas methane is essential for attributing the roles of anthropogenic activity and natural phenomena in global climate change. Our current measurement systems and networks, whilst having improved during the last decades, are deficient in many respects. For example, the emissions from localised and point sources such as landfills or fossil fuel exploration sites are not readily assessed. A tool developed to better understand point sources of the greenhouse gases carbon dioxide and methane is the optical remote sensing instrument MAMAP (Methane airborne MAPper), operated from aircraft. After a recent instrument modification, retrievals of the column-averaged dry air mole fractions for methane XCH4 (or for carbon dioxide XCO2) derived from MAMAP data have a precision of about 0.4% or better and thus can be used to infer emission rate estimates using an optimal estimation inverse Gaussian plume model or a simple integral approach. CH4 emissions from two coal mine ventilation shafts in western Germany surveyed during the AIRMETH 2011 measurement campaign are used as examples to demonstrate and assess the value of MAMAP data for quantifying CH4 from point sources. While the knowledge of the wind is an important input parameter in the retrieval of emissions from point sources and is generally extracted from models, additional information from a turbulence probe operated on-board the same aircraft was utilised to enhance the quality of the emission estimates. Although flight patterns were optimised for remote sensing measurements, data from an in situ analyser for CH4 were found to be in good agreement with retrieved dry columns of CH4 from MAMAP and could be used to investigate and refine underlying assumptions for the inversion procedures. With respect to the total emissions of the mine at the time of the overflight, the inferred emission rate of 50.4 kt CH4 yr-1 has a difference of less than 1% compared to officially

  19. Near-field beamforming analysis for acoustic emission source localization.

    PubMed

    He, Tian; Pan, Qiang; Liu, Yaoguang; Liu, Xiandong; Hu, Dayong

    2012-07-01

    This paper attempts to introduce a near-field acoustic emission (AE) beamforming method to estimate the AE source locations by using a small array of sensors closely placed in a local region. The propagation characteristics of AE signals are investigated based on guided wave theory to discuss the feasibility of using beamforming techniques in AE signal processing. To validate the effectiveness of the AE beamforming method, a series of pencil lead break tests at various regions of a thin steel plate are conducted. The potential of this method for engineering applications are explored through rotor-stator rubbing tests. The experimental results demonstrate that the proposed method can effectively determine the region where rubbing occurs. It is expected that the work of this paper may provide a helpful analysis tool for near-field AE source localization.

  20. Characterizing the isotopic composition of atmospheric ammonia emission sources using passive samplers and a combined oxidation-bacterial denitrifier approach

    USDA-ARS?s Scientific Manuscript database

    Ammonia (NH3) emissions are a substantial source of nitrogen pollution to sensitive terrestrial, aquatic, and marine ecosystems. Dependable quantification of NH3 sources is of growing importance due to recently observed increases in ammonium (NH4+) deposition rates that are directly proportional to ...

  1. What could have caused pre-industrial biomass burning emissions to exceed current rates?

    NASA Astrophysics Data System (ADS)

    van der Werf, G. R.; Peters, W.; van Leeuwen, T. T.; Giglio, L.

    2012-08-01

    Recent studies based on trace gas mixing ratios in ice cores and charcoal data indicate that biomass burning emissions over the past millennium exceeded contemporary emissions by up to a factor of 4 for certain time periods. This is surprising because various sources of biomass burning are linked with population density, which has increased over the past centuries. Here we have analyzed how emissions from several biomass burning sources could have fluctuated to yield emissions that are in correspondence with recent results based on ice core mixing ratios of carbon monoxide (CO) and its isotopic signature measured at South Pole station (SPO). Based on estimates of contemporary fire emissions and the TM5 chemical transport model, we found that CO mixing ratios at SPO are more sensitive to emissions from South America and Australia than from Africa, and are relatively insensitive to emissions from the Northern Hemisphere. We then explored how various biomass burning sources may have varied over the past centuries and what the resulting emissions and corresponding CO mixing ratio at SPO would be, using population density variations to reconstruct sources driven by humans (e.g. fuelwood burning) and a new model to relate savanna emissions to changes in fire return times. We found that to match the observed ice core CO data all savannas in the Southern Hemisphere had to burn annually, or bi-annually in combination with deforestation and slash and burn agriculture matching current levels despite much lower population densities and lack of machinery to aid the deforestation process. While possible, these scenarios are unlikely and in conflict with current literature. However, we do show the large potential for increased emissions from savannas in a pre-industrial world. This is mainly because in the past, fuel beds were probably less fragmented compared to the current situation; we show that the majority of savannas have not burned in the past 10 yr, even in Africa which

  2. What could have caused pre-industrial biomass burning emissions to exceed current rates?

    NASA Astrophysics Data System (ADS)

    van der Werf, G. R.; Peters, W.; van Leeuwen, T. T.; Giglio, L.

    2013-01-01

    Recent studies based on trace gas mixing ratios in ice cores and charcoal data indicate that biomass burning emissions over the past millennium exceeded contemporary emissions by up to a factor of 4 for certain time periods. This is surprising because various sources of biomass burning are linked with population density, which has increased over the past centuries. We have analysed how emissions from several landscape biomass burning sources could have fluctuated to yield emissions that are in correspondence with recent results based on ice core mixing ratios of carbon monoxide (CO) and its isotopic signature measured at South Pole station (SPO). Based on estimates of contemporary landscape fire emissions and the TM5 chemical transport model driven by present-day atmospheric transport and OH concentrations, we found that CO mixing ratios at SPO are more sensitive to emissions from South America and Australia than from Africa, and are relatively insensitive to emissions from the Northern Hemisphere. We then explored how various landscape biomass burning sources may have varied over the past centuries and what the resulting emissions and corresponding CO mixing ratio at SPO would be, using population density variations to reconstruct sources driven by humans (e.g., fuelwood burning) and a new model to relate savanna emissions to changes in fire return times. We found that to match the observed ice core CO data, all savannas in the Southern Hemisphere had to burn annually, or bi-annually in combination with deforestation and slash and burn agriculture exceeding current levels, despite much lower population densities and lack of machinery to aid the deforestation process. While possible, these scenarios are unlikely and in conflict with current literature. However, we do show the large potential for increased emissions from savannas in a pre-industrial world. This is mainly because in the past, fuel beds were probably less fragmented compared to the current situation

  3. Investigating aircraft-based emissions estimates using GEM-MACH with the top-down emission rate retrieval algorithm (TERRA)

    NASA Astrophysics Data System (ADS)

    Fathi, S.; Gordon, M.; Makar, P.; Li, S. M.; Darlington, A. L.; Akingunola, A.; Zhang, J.; Moran, M. D.; Zheng, Q.

    2016-12-01

    Between August 13th and September 7th of 2013, aircraft-based measurements of air pollutants were collected in support of the Joint Canada-Alberta Implementation Plan on Oil Sands Monitoring. The Top-down Emission Rate Retrieval Algorithm (TERRA) was developed by Environment and Climate Change Canada to estimate facility emission rates based on the aircraft measurements (Gordon et al, 2015). TERRA as applied to date uses aircraft observations of emitted pollutants, wind speed and direction, to create two-dimensional screens surrounding an emitting facility; the transport through these screens and the divergence theorem is used to generate observation-based emissions estimates. Here, as part of a larger effort on TERRA improvement, Environment and Climate Change Canada's air quality model, Global Environmental Multiscale-Modeling Air-quality and CHemistry (GEM-MACH), was used as a surrogate source of concentration and meteorology data. We investigate the potential of this approach for improving the known uncertainties in the TERRA schemes of extrapolation to the surface from the lowest flight altitudes of 150 meters above ground, and as a check on the accuracy of GEM-MACH. Linear interpolation in time and space of GEM-MACH's 2.5km-resolution/2-minute time-step output fields to the aircraft's observed locations were used as TERRA inputs. The TERRA-calculated emission rates are compared with those input into GEM-MACH, for different TERRA configurations. The work evaluates the combination of TERRA and GEM-MACH as a proxy for testing the downward extrapolation schemes within TERRA and identifies possible avenues for GEM-MACH and/or TERRA improvements. Outcomes from this work can provide useful suggestions for future flight plans for top-down emission rate estimations. Reference: M. Gordon, S.-M. Li, R. Staebler, A. Darlington, K. Hayden, J. O'Brien, M. Wolde, Determining air pollutant emission rates based on mass balance using airborne measurement data over the Alberta

  4. POLYCYCLIC AROMATIC HYDROCARBON CLUSTERS AS SOURCES OF INTERSTELLAR INFRARED EMISSION

    SciTech Connect

    Roser, J. E.; Ricca, A.

    2015-03-10

    Polycyclic aromatic hydrocarbons (or PAHs) have been the subject of astrochemical research for several decades as principal sources of the interstellar aromatic infrared emission bands. PAH clusters could possibly contribute to these emission bands, but a lack of data on their infrared properties has made this hypothesis difficult to evaluate. Here we investigate homogeneous neutral PAH clusters by measuring the mid-infrared absorption spectra of the five nonlinear PAH molecules phenanthrene, chrysene, pyrene, perylene, and benzo[ghi]perylene within solid argon ice at a fixed temperature of 5 K. We attribute observed spectral shifts in their principal absorption bands as a function of argon/PAH ratio to clustering of the PAH molecules within the argon matrix. These shifts are related to the cluster structures forming in the matrix and the topology of the monomer PAH molecule. We predict that interstellar PAH molecules that are relatively large (no fewer than 50 carbon atoms per molecule) and compact will have clusters that contribute to the asymmetrically red-shaded profile of the interstellar 11.2 μm emission band.

  5. PAH Clusters as Sources of Interstellar Infrared Emission

    NASA Astrophysics Data System (ADS)

    Roser, J. E.; Ricca, A.

    2015-03-01

    Polycyclic aromatic hydrocarbons (or PAHs) have been the subject of astrochemical research for several decades as principal sources of the interstellar aromatic infrared emission bands. PAH clusters could possibly contribute to these emission bands, but a lack of data on their infrared properties has made this hypothesis difficult to evaluate. Here we investigate homogeneous neutral PAH clusters by measuring the mid-infrared absorption spectra of the five nonlinear PAH molecules phenanthrene, chrysene, pyrene, perylene, and benzo[ghi]perylene within solid argon ice at a fixed temperature of 5 K. We attribute observed spectral shifts in their principal absorption bands as a function of argon/PAH ratio to clustering of the PAH molecules within the argon matrix. These shifts are related to the cluster structures forming in the matrix and the topology of the monomer PAH molecule. We predict that interstellar PAH molecules that are relatively large (no fewer than 50 carbon atoms per molecule) and compact will have clusters that contribute to the asymmetrically red-shaded profile of the interstellar 11.2 μm emission band.

  6. The Sources of F10.7 Emission

    NASA Astrophysics Data System (ADS)

    Schonfeld, Samuel; White, Stephen; Henney, Carl; Arge, Nick; McAteer, James

    2015-04-01

    The solar radio flux at a wavelength of 10.7 cm, F10.7, serves as a proxy for the Sun’s ionizing flux striking the Earth and is a heavily used index for space weather studies. In principal both the coronal sources of ionizing flux and strong coronal magnetic fields contribute to F10.7 via the bremsstrahlung and gyroresonance mechanisms respectively. Recently the Karl G. Jansky Very Large Array (JVLA) has added the capability to make high-spatial-resolution images of the Sun at 10.7 cm. We present the results of a trial study comparing an F10.7 image from the JVLA with the bremsstrahlung emission predicted to be present. The predicted bremsstrahlung image is calculated with spatially resolved differential emission measures derived from extreme ultra-violet images of the Sun acquired by the Atmospheric Imaging Assembly. Photospheric magnetograms are used to identify likely regions of strong coronal magnetic field, and the circular polarization measured by the JVLA is used as a tracer of gyroresonance contributions. We find that only a small fraction of the variable F10.7 flux can be attributed to gyroresonance emission.

  7. Sources and emission of greenhouse gases in Danube Delta lakes.

    PubMed

    Pavel, Alina; Durisch-Kaiser, Edith; Balan, Sorin; Radan, Silviu; Sobek, Sebastian; Wehrli, Bernhard

    2009-08-01

    Production of methane and carbon dioxide as well as methane concentrations in surface waters and emissions to the atmosphere were investigated in two flow-through lake complexes (Uzlina-Isac and Puiu-Rosu-Rosulet) in the Danube Delta during post-flood conditions in May and low water level in September 2006. Retained nutrients fueled primary production and remineralization of bioavailable organic matter. This led to an observable net release of methane, particularly in the lakes Uzlina, Puiu and Rosu in May. Input from the Danube River, from redbuds and benthic release contributed to CH(4) concentrations in surface waters. In addition to significant river input of CO(2), this trace gas was released via aerobic remineralization within the water column and in top sediments. Emission patterns of CO(2) widely overlapped with those of CH(4). Generally, greenhouse gas emissions peaked in the lake complex adjacent to the Danube River in May due to strong winds and decreased with increasing hydrological distance from the Danube River. Intense remineralization of organic matter in the Danube Delta lakes results in a net source of atmospheric greenhouse gases.

  8. Modeling the H2O submillimeter emission in extragalactic sources

    NASA Astrophysics Data System (ADS)

    González-Alfonso, E.; Fischer, J.; Aalto, S.; Falstad, N.

    2014-07-01

    Recent observational studies have shown that H2O emission at (rest) submillimeter wavelengths is ubiquitous in infrared galaxies, both in the local and in the early Universe, suggestive of far-infrared pumping of H2O by dust in warm regions. In this work, models are presented that show that (i) the highest-lying H2O lines (Eupper > 400 K) are formed in very warm (Tdust ≳ 90 K) regions and require high H2O columns (NH2O ≳ 3 × 1017 cm-2), while lower lying lines can be efficiently excited with Tdust ~ 45-75 K and NH2O ~ (0.5-2) × 1017 cm-2; (ii) significant collisional excitation of the lowest lying (Eupper < 200 K) levels, which enhances the overall LH2O-LIR ratios, is identified in sources where the ground-state para-H2O 111-000 line is detected in emission; (iii) the H2O-to-infrared (8-1000 μm) luminosity ratio is expected to decrease with increasing Tdust for all lines with Eupper ≲ 300 K, as has recently been reported in a sample of LIRGs, but increases with Tdust for the highest lying H2O lines (Eupper > 400 K); (iv) we find theoretical upper limits for LH2O/LIR in warm environments, owing to H2O line saturation; (v) individual models are presented for two very different prototypical galaxies, the Seyfert 2 galaxy NGC 1068 and the nearest ultraluminous infrared galaxy Arp 220, showing that the excited submillimeter H2O emission is dominated by far-infrared pumping in both cases; (vi) the LH2O - LIR correlation previously reported in observational studies indicates depletion or exhaustion time scales, tdep = Σgas/ ΣSFR, of ≲12 Myr for star-forming sources where lines up to Eupper = 300 K are detected, in agreement with the values previously found for (U)LIRGs from HCN millimeter emission. We conclude that the submillimeter H2O line emission other than the para-H2O 111-000 transition is pumped primarily by far-infrared radiation, though some collisional pumping may contribute to the low-lying para-H2O 202-111 line, and that collisional pumping of the

  9. Measurements of Point Source Methane Emissions in the Barnett Shale and Eagle Ford Basins

    NASA Astrophysics Data System (ADS)

    Lavoie, T. N.; Shepson, P. B.; Cambaliza, M. O. L.; Karion, A.; Sweeney, C.; Kort, E. A.; Hirst, B.; Wolter, S.; Conley, S. A.; Faloona, I. C.; Lyon, D.; Alvarez, R.

    2014-12-01

    The global average temperature is rising as a result of anthropogenic emissions of greenhouse gases. The two organic carbon gases that contribute most to this warming are carbon dioxide (CO2) and methane (CH4). CH4, however, is 34 times more potent as a greenhouse gas than CO2 on a 100-year timescale, and 86 times more potent on a 20-year timescale. The ~12 year lifetime of CH4 means that measures to control methane emissions on the near-term time scale may have a relatively large climate benefit. The past decade has witnessed a dramatic increase in the reliance on natural gas (NG) to meet the energy needs of the U.S. To enable informed greenhouse gas policy and mitigation efforts, a comprehensive understanding of the nature and magnitude of CH4 emissions for various related NG technologies and engineering practices is required. Here we report results of our recent studies of the CH4 emission rate observed at eight different biogenic and NG point sources in the Barnett shale basin and a dozen well pads in the Eagle Ford shale region of Texas. We compare our field measurements to reported inventory estimates from the Greenhouse Gas Reporting Program (GHGRP). Using an aircraft-based mass balance approach, we found that the summed observed CH4 emission rates for our study sites were a factor of 2.5 to 4.5 greater than the GHGRP-based estimates, for the 8 sources we investigated in the Barnett shale region. The sum of the 5 Barnett NG sources we quantified had on average CH4 emissions 17.5X higher than the GHGRP inventory indicates. The sum of the 3 landfill emission rates were on average 1.5X greater than the inventory values. In the Eagle Ford shale region, high variability was observed in repeated measurements at the same well pads, highlighting the difficulty of assessing the character and statistics of the distribution of emissions from individual pads. These results indicate a need for better methods of emissions monitoring and reporting and highlight the

  10. Neutron-emission measurements at a white neutron source

    SciTech Connect

    Haight, Robert C

    2010-01-01

    Data on the spectrum of neutrons emittcd from neutron-induced reactions are important in basic nuclear physics and in applications. Our program studies neutron emission from inelastic scattering as well as fission neutron spectra. A ''white'' neutron source (continuous in energy) allows measurements over a wide range of neutron energies all in one experiment. We use the tast neutron source at the Los Alamos Neutron Science Center for incident neutron energies from 0.5 MeV to 200 MeV These experiments are based on double time-of-flight techniques to determine the energies of the incident and emitted neutrons. For the fission neutron measurements, parallel-plate ionization or avalanche detectors identify fission in actinide samples and give the required fast timing pulse. For inelastic scattering, gamma-ray detectors provide the timing and energy spectroscopy. A large neutron-detector array detects the emitted neutrons. Time-of-flight techniques are used to measure the energies of both the incident and emitted neutrons. Design considerations for the array include neutron-gamma discrimination, neutron energy resolution, angular coverage, segmentation, detector efficiency calibration and data acquisition. We have made preliminary measurements of the fission neutron spectra from {sup 235}U, {sup 238}U, {sup 237}Np and {sup 239}Pu. Neutron emission spectra from inelastic scattering on iron and nickel have also been investigated. The results obtained will be compared with evaluated data.

  11. Effects of mass airflow rate through an open-circuit gas quantification system when measuring carbon emissions.

    PubMed

    Gunter, Stacey A; Bradford, James A; Moffet, Corey A

    2017-01-01

    Methane (CH) and carbon dioxide (CO) represent 11 and 81%, respectively, of all anthropogenic greenhouse gas emissions. Agricultural CH emissions account for approximately 43% of all anthropogenic CH emissions. Most agricultural CH emissions are attributed to enteric fermentation within ruminant livestock; hence, the heightened interest in quantifying and mitigating this source. The automated, open-circuit gas quantification system (GQS; GreenFeed, C-Lock, Inc., Rapid City, SD) evaluated here can be placed in a pasture with grazing cattle and can measure their CH and CO emissions with spot sampling. However, improper management of the GQS can have an erroneous effect on emission estimates. One factor affecting the quality of emission estimates is the airflow rates through the GQS to ensure a complete capture of the breath cloud emitted by the animal. It is hypothesized that at lower airflow rates this cloud will be incompletely captured. To evaluate the effect of airflow rate through the GQS on emission estimates, a data set was evaluated with 758 CO and CH emission estimates with a range in airflows of 10.7 to 36.6 L/s. When airflow through the GQS was between 26.0 and 36.6 L/s, CO and CH emission estimates were not affected ( = 0.14 and 0.05, respectively). When airflow rates were less than 26.0 L/s, CO and CH emission estimates were lower and decreased as airflow rate decreased ( < 0.0001). We hypothesize that when airflow through the GQS decreases below 26 L/s, breath capture was incomplete and CO and CH emissions are underestimated. Maintaining mass airflow through a GQS at rates greater than 26 L/s is important for producing high quality CO and CH emission estimates.

  12. Nitrogen placement and source effects on nitrous oxide emissions and yields of irrigated corn.

    PubMed

    Halvorson, Ardell D; Del Grosso, Stephen J

    2013-01-01

    Limited information is available on how N fertilizer placement affects soil nitrous oxide (NO) emissions under irrigated conditions in the semiarid western United States. Our objective was to compare surface banding near corn row and broadcasting of three N sources (urea, polymer-coated urea [PCU], and stabilized urea [SU] containing urease and nitrification inhibitors) on NO emissions from a clay loam soil under sprinkler-irrigated continuous corn production. The N fertilizers were applied at a rate of 202 kg N ha to strip-till (2010 and 2011) and no-till (2011) corn at crop emergence, with ∼19 mm irrigation water applied the next day. Band-applied N had a 1.46-fold greater NO emission than broadcast N averaged over N sources and three studies. Soil NO-N emissions from urea were 1.48- and 1.74-fold greater than from PCU and SU, respectively, when averaged over N placement and studies. The N placement × source interaction was not significant. Averaged across studies, grain yield and N uptake did not vary with N placement, whereas grain yields were greater for SU than PCU but were not different from urea. Nitrous oxide emissions per unit of N applied, per unit of grain yield, and per unit N uptake were 59, 49, and 47% greater, respectively, with banded than with broadcast N fertilizer. These studies show that N placement and N source selection are important manageable factors that can affect NO emissions and need to be considered when developing NO mitigation practices in irrigated cropping systems in the semiarid western United States. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

  13. Atmospheric Modeling and Verification of Point Source Fossil Fuel CO2 Emissions

    NASA Astrophysics Data System (ADS)

    Keller, E. D.; Turnbull, J. C.; Baisden, W. T.; Brailsford, G. W.; Bromley, T.; Norris, M. W.; Zondervan, A.

    2014-12-01

    Emissions from large point sources (electricity generation and large-scale industry) of fossil fuel CO2 (CO2ff) emissions are currently determined from self-reported "bottom-up" inventory data, with an uncertainty of about 20% for individual power plants. As the world moves towards a regulatory environment, there is a need for independent, objective measurements of these emissions both to improve the accuracy of and to verify the reported amounts. "Top-down" atmospheric methods have the potential to independently constrain point source emissions, combining observations with atmospheric transport modeling to derive emission estimates. We use the Kapuni Gas Treatment Plant to examine methodologies and model sensitivities for atmospheric monitoring of point source fossil fuel CO2 (CO2ff) emissions. The Kapuni plant, located in rural New Zealand, removes and vents CO2 from locally extracted natural gas at a rate of ~0.1 Tg carbon per year. We measured the CO2ff content in three different types of observations: air samples collected in flasks over a period of a few minutes, sodium hydroxide solution exposed the atmosphere, and grass samples from the surrounding farmland, the latter two representing ~1 week integrated averages. We use the WindTrax Lagrangian plume dispersion model to compare these atmospheric observations with "expected" values given the emissions reported by the Kapuni plant. The model has difficulty accurately capturing the short-term variability in the flask samples but does well in representing the longer-term averages from grass samples, suggesting that passive integrated-sampling methods have the potential to monitor long-term emissions. Our results indicate that using this method, point source emissions can be verified to within about 30%. Further improvements in atmospheric transport modelling are needed to reduce uncertainties. In view of this, we discuss model strengths and weaknesses and explore model sensitivity to meteorological conditions

  14. Modal acoustic emission source determination in silicon carbide matrix composites

    NASA Astrophysics Data System (ADS)

    Morscher, G. N.

    2000-05-01

    Modal acoustic emission has been used to monitor damage accumulation in woven silicon carbide (SiC) fiber reinforced SiC matrix composites during tensile testing. There are several potential sources of damage in these systems including transverse matrix cracking, fiber/matrix interphase debonding and sliding, longitudinal cracks in between plies, and fiber breakage. In the past, it has been shown that modal AE is excellent at detecting when damage occurs and subsides, where the damage occurs along the length of the sample, and the loss in material stiffness as a consequence of damage accumulation. The next step is to determine the extent that modal AE can be used to identify specific physical sources. This study will discuss the status of this aim for this composite system. Individual events were analyzed and correlated to specific sources based on the characteristics of the received waveforms, e.g., frequency spectrum and energy, and when the event occurred during the stress-history of the tensile test. Post-test microstructural examination of the test specimens enabled some correlation between specific types of AE events and damage sources.

  15. Odd-even staggering of heavy cluster spontaneous emission rates

    NASA Astrophysics Data System (ADS)

    Poenaru, D. N.; Greiner, W.; Ivaşcu, M.; Mazilu, D.; Plonski, I. H.

    1986-12-01

    Experimentally observed enhanced14C and24Ne emission rates from even-even parents in comparison with that from even-odd or odd-even nuclei are explained in the framework of the analytical superasymmetric fission model, by taking various prescriptions for the zero point vibration energy of even-even, even-odd, odd-even and odd-odd emitters. Longer half-lives than previously computed are obtained by extrapolating the present prescriptions to emitted clusters heavier than24Ne.

  16. Identifying and characterizing major emission point sources as a basis for geospatial distribution of mercury emissions inventories

    NASA Astrophysics Data System (ADS)

    Steenhuisen, Frits; Wilson, Simon J.

    2015-07-01

    Mercury is a global pollutant that poses threats to ecosystem and human health. Due to its global transport, mercury contamination is found in regions of the Earth that are remote from major emissions areas, including the Polar regions. Global anthropogenic emission inventories identify important sectors and industries responsible for emissions at a national level; however, to be useful for air transport modelling, more precise information on the locations of emission is required. This paper describes the methodology applied, and the results of work that was conducted to assign anthropogenic mercury emissions to point sources as part of geospatial mapping of the 2010 global anthropogenic mercury emissions inventory prepared by AMAP/UNEP. Major point-source emission sectors addressed in this work account for about 850 tonnes of the emissions included in the 2010 inventory. This work allocated more than 90% of these emissions to some 4600 identified point source locations, including significantly more point source locations in Africa, Asia, Australia and South America than had been identified during previous work to geospatially-distribute the 2005 global inventory. The results demonstrate the utility and the limitations of using existing, mainly public domain resources to accomplish this work. Assumptions necessary to make use of selected online resources are discussed, as are artefacts that can arise when these assumptions are applied to assign (national-sector) emissions estimates to point sources in various countries and regions. Notwithstanding the limitations of the available information, the value of this procedure over alternative methods commonly used to geo-spatially distribute emissions, such as use of 'proxy' datasets to represent emissions patterns, is illustrated. Improvements in information that would facilitate greater use of these methods in future work to assign emissions to point-sources are discussed. These include improvements to both national

  17. Source identification of benzene emissions in Texas City using an adjoint neighborhood scale transport model

    NASA Astrophysics Data System (ADS)

    Guven, B.; Olaguer, E. P.; Herndon, S. C.; Kolb, C. E.; Cuclis, A.

    2012-12-01

    During the "Formaldehyde and Olefins from Large Industrial Sources" (FLAIR) study in 2009, the Aerodyne Research Inc. (ARI) mobile laboratory performed real-time in situ measurements of VOCs, NOx and HCHO in Texas City, TX on May 7, 2009 from 11 am to 3 pm. This high resolution dataset collected in a predominantly industrial area provides an ideal test bed for advanced source attribution. Our goal was to identify and quantify emission sources within the largest facility in Texas City most likely responsible for measured benzene concentrations. For this purpose, fine horizontal resolution (200 m x 200 m) 4D variational (4Dvar) inverse modeling was performed by running the HARC air quality transport model in adjoint mode based on ambient concentrations measured by the mobile laboratory. The simulations were conducted with a horizontal domain size of 4 km x 4 km for a four-hour period (11 am to 3 pm). Potential emission unit locations within the facility were specified using a high spatial resolution digital model of the largest industrial complex in the area. The HARC model was used to infer benzene emission rates from all potential source locations that would account for the benzene concentrations measured by the Aerodyne mobile laboratory in the vicinity of the facility. A Positive Matrix Factorization receptor model was also applied to the concentrations of other compounds measured by the mobile lab to support the source attribution by the inverse model. Although previous studies attributed measured benzene concentrations during the same time period to a cooling tower unit at the industrial complex, this study found that some of the flare units in the facility were also associated with the elevated benzene concentrations. The emissions of some of these flare units were found to be greater than reported in emission inventories, by up to two orders of magnitude.

  18. Size-resolved emission rates of airborne bacteria and fungi in an occupied classroom

    PubMed Central

    Qian, J; Hospodsky, D; Yamamoto, N; Nazaroff, W W; Peccia, J

    2012-01-01

    The role of human occupancy as a source of indoor biological aerosols is poorly understood. Size-resolved concentrations of total and biological particles in indoor air were quantified in a classroom under occupied and vacant conditions. Per-occupant emission rates were estimated through a mass-balance modeling approach, and the microbial diversity of indoor and outdoor air during occupancy was determined via rDNA gene sequence analysis. Significant increases of total particle mass and bacterial genome concentrations were observed during the occupied period compared to the vacant case. These increases varied in magnitude with the particle size and ranged from 3 to 68 times for total mass, 12–2700 times for bacterial genomes, and 1.5–5.2 times for fungal genomes. Emission rates per person-hour because of occupancy were 31 mg, 37 × 106 genome copies, and 7.3 × 106 genome copies for total particle mass, bacteria, and fungi, respectively. Of the bacterial emissions, ∼18% are from taxa that are closely associated with the human skin microbiome. This analysis provides size-resolved, per person-hour emission rates for these biological particles and illustrates the extent to which being in an occupied room results in exposure to bacteria that are associated with previous or current human occupants. Practical Implications Presented here are the first size-resolved, per person emission rate estimates of bacterial and fungal genomes for a common occupied indoor space. The marked differences observed between total particle and bacterial size distributions suggest that size-dependent aerosol models that use total particles as a surrogate for microbial particles incorrectly assess the fate of and human exposure to airborne bacteria. The strong signal of human microbiota in airborne particulate matter in an occupied setting demonstrates that the aerosol route can be a source of exposure to microorganisms emitted from the skin, hair, nostrils, and mouths of other occupants

  19. Size-resolved emission rates of airborne bacteria and fungi in an occupied classroom.

    PubMed

    Qian, J; Hospodsky, D; Yamamoto, N; Nazaroff, W W; Peccia, J

    2012-08-01

    The role of human occupancy as a source of indoor biological aerosols is poorly understood. Size-resolved concentrations of total and biological particles in indoor air were quantified in a classroom under occupied and vacant conditions. Per-occupant emission rates were estimated through a mass-balance modeling approach, and the microbial diversity of indoor and outdoor air during occupancy was determined via rDNA gene sequence analysis. Significant increases of total particle mass and bacterial genome concentrations were observed during the occupied period compared to the vacant case. These increases varied in magnitude with the particle size and ranged from 3 to 68 times for total mass, 12-2700 times for bacterial genomes, and 1.5-5.2 times for fungal genomes. Emission rates per person-hour because of occupancy were 31 mg, 37 × 10(6) genome copies, and 7.3 × 10(6) genome copies for total particle mass, bacteria, and fungi, respectively. Of the bacterial emissions, ∼18% are from taxa that are closely associated with the human skin microbiome. This analysis provides size-resolved, per person-hour emission rates for these biological particles and illustrates the extent to which being in an occupied room results in exposure to bacteria that are associated with previous or current human occupants. Presented here are the first size-resolved, per person emission rate estimates of bacterial and fungal genomes for a common occupied indoor space. The marked differences observed between total particle and bacterial size distributions suggest that size-dependent aerosol models that use total particles as a surrogate for microbial particles incorrectly assess the fate of and human exposure to airborne bacteria. The strong signal of human microbiota in airborne particulate matter in an occupied setting demonstrates that the aerosol route can be a source of exposure to microorganisms emitted from the skin, hair, nostrils, and mouths of other occupants. © 2012 John Wiley

  20. Mercury emissions to the atmosphere from natural and anthropogenic sources in the Mediterranean region

    NASA Astrophysics Data System (ADS)

    Pirrone, N.; Costa, P.; Pacyna, J. M.; Ferrara, R.

    This report discusses past, current and projected mercury emissions to the atmosphere from major industrial sources, and presents a first assessment of the contribution to the regional mercury budget from selected natural sources. Emissions (1995 estimates) from fossil fuels combustion (29.8 t yr -1) , cement production (28.8 t yr -1) and incineration of solid wastes (27.6 t yr -1) , all together account for about 82% of the regional anthropogenic total (105.7 t yr -1) . Other industrial sources in the region are smelters (4.8 t yr -1) , iron-steel plants (4.8 t yr -1) and other minor sources (chlor-alkali plants, crematoria, chemicals production) that have been considered together in the miscellaneous category (9.6 t yr -1) . Regional emissions from anthropogenic sources increased at a rate of 3% yr-1 from 1983 to 1995 and are projected to increase at a rate of 1.9% yr-1 in the next 25 years, if no improvement in emission control policy occurs. On a country-by-country basis, France is the leading emitter country with 22.6 t yr -1 followed by Turkey (16.1 t yr -1) , Italy (11.4 t yr -1) , Spain (9.1 t yr -1) , the former Yugoslavia 7.9 ( t yr -1) , Morocco (6.9 t yr -1) , Bulgaria (6.8 t yr -1) , Egypt (6.1 t yr -1) , Syria (3.6 t yr -1) , Libya (2.9 t yr -1) , Tunisia (2.8 t yr -1) and Greece (2.7 t yr -1) , whereas the remaining countries account for less than 7% of the regional total. The annual emission from natural sources is 110 t yr -1, although this figure only includes the volatilisation of elemental mercury from surface waters and emissions from volcanoes, whereas the contribution due to the degassing of mercury from top soil and vegetation has not been included in this first assessment. Therefore, natural and anthropogenic sources in the Mediterranean region release annually about 215 t of mercury, which represents a significant contribution to the total mercury budget released in Europe and to the global atmosphere.

  1. Variability of OH(3-1) and OH(6-2) emission altitude and volume emission rate from 2003 to 2011

    NASA Astrophysics Data System (ADS)

    Teiser, Georg; von Savigny, Christian

    2017-08-01

    In this study we report on variability in emission rate and centroid emission altitude of the OH(3-1) and OH(6-2) Meinel bands in the terrestrial nightglow based on spaceborne nightglow measurements with the SCIAMACHY (SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY) instrument on the Envisat satellite. The SCIAMACHY observations cover the time period from August 2002 to April 2012 and the nighttime observations used in this study are performed at 10:00 p.m. local solar time. Characterizing variability in OH emission altitude - particularly potential long-term variations - is important for an appropriate interpretation of ground-based OH rotational temperature measurements, because simultaneous observations of the vertical OH volume emission rate profile are usually not available for these measurements. OH emission altitude and vertically integrated emission rate time series with daily resolution for the OH(3-1) band and monthly resolution for the OH(6-2) band were analyzed using a standard multilinear regression approach allowing for seasonal variations, QBO-effects (Quasi-Biennial Oscillation), solar cycle (SC) variability and a linear long-term trend. The analysis focuses on low latitudes, where SCIAMACHY nighttime observations are available all year. The dominant sources of variability for both OH emission rate and altitude are the semi-annual and annual variations, with emission rate and altitude being highly anti-correlated. There is some evidence for a 11-year solar cycle signature in the vertically integrated emission rate and in the centroid emission altitude of both the OH(3-1) and OH(6-2) bands.

  2. Atmospheric dispersion modeling with AERMOD for comparative impact assessment of different pollutant emission sources in an Alpine context

    NASA Astrophysics Data System (ADS)

    Antonacci, Gianluca; Giovannini, Lorenzo; Tomasi, Elena; Zardi, Dino

    2015-04-01

    High-resolution simulations are performed with the AERMOD model to analyze the impact on air quality of different pollutant emission sources in the area surrounding the town of Vipiteno in the northeastern Italian Alps. In this area the environmental burden of pollutant emissions is particularly high because of both its complex terrain and the presence of specific pollutant sources. In this study the effects of the main sources are analyzed and compared: the A22 motorway, which leads to the Brenner pass, the town of Vipiteno, mainly characterized by intensive use of biomass for house heating, three major plants with high emission rates, and a parking lot located near the motorway, offering park spaces for up to 260 trucks and 50 cars. To assess the impact of these pollution sources the AERMOD model is run with a spatial resolution of 25 m and with meteorological input data obtained from different datasets, such as annual series of standard meteorological variables taken from local weather stations and a set of vertical soundings. During the simulations the sources are modeled in different ways depending on the type of the emissions: the motorway is modeled as a linear source, the village as a diffuse source, the local companies as point sources and the parking lot is modeled as a composition of a diffuse source, representing the idling vehicles inside the park, and of a linear source, representing the access routes to the parking. For each type of source, specific emission factors are chosen, and hourly and seasonal emission patterns are set with particular attention to the analysis of idling vehicle emission factors. The results of the simulations are analyzed in terms of NO2 and PM10 and the impact of each source is discussed.

  3. Open-source LCA tool for estimating greenhouse gas emissions from crude oil production using field characteristics.

    PubMed

    El-Houjeiri, Hassan M; Brandt, Adam R; Duffy, James E

    2013-06-04

    Existing transportation fuel cycle emissions models are either general and calculate nonspecific values of greenhouse gas (GHG) emissions from crude oil production, or are not available for public review and auditing. We have developed the Oil Production Greenhouse Gas Emissions Estimator (OPGEE) to provide open-source, transparent, rigorous GHG assessments for use in scientific assessment, regulatory processes, and analysis of GHG mitigation options by producers. OPGEE uses petroleum engineering fundamentals to model emissions from oil and gas production operations. We introduce OPGEE and explain the methods and assumptions used in its construction. We run OPGEE on a small set of fictional oil fields and explore model sensitivity to selected input parameters. Results show that upstream emissions from petroleum production operations can vary from 3 gCO2/MJ to over 30 gCO2/MJ using realistic ranges of input parameters. Significant drivers of emissions variation are steam injection rates, water handling requirements, and rates of flaring of associated gas.

  4. Optimized source selection for intracavitary low dose rate brachytherapy

    SciTech Connect

    Nurushev, T.; Kim, Jinkoo

    2005-05-01

    A procedure has been developed for automating optimal selection of sources from an available inventory for the low dose rate brachytherapy, as a replacement for the conventional trial-and-error approach. The method of optimized constrained ratios was applied for clinical source selection for intracavitary Cs-137 implants using Varian BRACHYVISION software as initial interface. However, this method can be easily extended to another system with isodose scaling and shaping capabilities. Our procedure provides optimal source selection results independent of the user experience and in a short amount of time. This method also generates statistics on frequently requested ideal source strengths aiding in ordering of clinically relevant sources.

  5. Optical nanoantennas: controlled emission of single photon sources

    NASA Astrophysics Data System (ADS)

    van Hulst, Niek

    2011-03-01

    Nanoscale quantum emitters are key elements in quantum optics and sensing. However, efficient optical excitation and detection of such emitters involves large solid angles, due to their omnidirectional interaction with freely propagating light and due to limits of diffraction. Optical nanoantennas offer both nanoscale localization and efficient interaction. Here we focus on the control of the interaction of single photon emitters (molecules, quantum dots) with radiation through metal nanorod antennas. First a novel analytical model is presented, which shows the continuous evolution of the properties of optical antennas as they become increasingly bound, i.e. plasmonic. The model accurately describes the complete emission process, the radiative decay rate, quantum efficiency, and angular emission, moreover gives a quantitative description of the gradual emergence of sub-radiant, super-radiant, and dark modes. Next we investigate experimentally the coupling of a single quantum dot to a nanorod of increasing length. The angular luminescence of the quantum dot is detected through increasingly higher order antenna modes. Simultaneously the emission is strongly polarized and enhanced. Direct confrontation with theory allows to determine the coupling efficiency of the quantum dot to the antenna. Finally, we present unidirectional emission of a single emitter by coupling to a nanofabricated Yagi-Uda antenna. A quantum dot is placed in the near field of the antenna so that it drives the resonant feed element of the antenna. The resulting quantum-dot luminescence is strongly polarized and highly directed into a narrow forward angular cone. The directionality of the quantum dot can be controlled by tuning the antenna dimensions. Thus our results show the potential of optical antennas to communicate energy to, from, and between nano-emitters. A.G.Curto et al., Science 329, 930 (2010)

  6. Characterization of gaseous pollutant and particulate matter emission rates from a commercial broiler operation part I: Observed trends in emissions

    NASA Astrophysics Data System (ADS)

    Roumeliotis, Taylor S.; Dixon, Brad J.; Van Heyst, Bill J.

    2010-10-01

    This paper characterizes the emission rates of size fractionated particulate matter, inorganic aerosols, acid gases, ammonia and methane measured over four flocks at a commercial broiler chicken facility. Mean emission rates of each pollutant, along with sampling notes, were reported in this paper, the first in a series of two. Sampling notes were needed because inherent gaps in data may bias the mean emission rates. The mean emission rates of PM 10 and PM 2.5 were 5.0 and 0.78 g day -1 [Animal Unit, AU] -1, respectively, while inorganic aerosols mean emission rates ranged from 0.15 to 0.46 g day -1 AU -1 depending on the season. The average total acid gas emission rate was 0.43 g day -1 AU -1 with the greatest contribution from nitrous and nitric acids and little contribution from sulfuric acid (as SO 2). Ammonia emissions were seasonally dependent, with a mean emission rate of 66.0 g day -1 AU -1 in the cooler seasons and 94.5 g day -1 AU -1 during the warmer seasons. Methane emissions were relatively consistent with a mean emission rate of 208 g day -1 AU -1. The diurnal pattern in each pollutant's emission rate was relatively consistent after normalizing the hourly emissions according to each daily mean emission rate. Over the duration of a production cycle, all the measured pollutants' emissions increased proportionally to the total live mass of birds in the house, with the exception of ammonia. Interrelationships between pollutants provide evidence of mutually dependent release mechanisms, which suggests that it may be possible to fill data gaps with minimal data requirements. In the second paper (Roumeliotis, T.S., Dixon, B.J., Van Heyst, B.J. Characterization of gaseous pollutants and particulate matter emission rates from a commercial broiler operation part II: correlated emission rates. Atmospheric Environment, 2010.), regression correlations are developed to estimate daily mean emission rates for data gaps and, using the normalized hourly diurnal

  7. Quantum Communication with a High-Rate Entangled Photon Source

    NASA Technical Reports Server (NTRS)

    Wilson, Nathaniel C.; Chaffee, Dalton W.; Lekki, John D.; Wilson, Jeffrey D.

    2016-01-01

    A high generation rate photon-pair source using a dual element periodically-poled potassium titanyl phosphate (PP KTP) waveguide is described. The photon-pair source features a high pair generation rate, a compact power-efficient package, and continuous wave (CW) or pulsed operation. Characterization and test results are presented. Details and preliminary results of a laboratory free-space QKD experiment with the B92 protocol are also presented.

  8. Development of a composite line source emission model for traffic interrupted microenvironments and its application in particle number emissions at a bus station

    NASA Astrophysics Data System (ADS)

    Wang, Lina; Jayaratne, Rohan; Heuff, Darlene; Morawska, Lidia

    A composite line source emission (CLSE) model was developed to specifically quantify exposure levels and describe the spatial variability of vehicle emissions in traffic interrupted microenvironments. This model took into account the complexity of vehicle movements in the queue, as well as different emission rates relevant to various driving conditions (cruise, decelerate, idle and accelerate), and it utilised multi-representative segments to capture the accurate emission distribution for real vehicle flow. Hence, this model was able to quickly quantify the time spent in each segment within the considered zone, as well as the composition and position of the requisite segments based on the vehicle fleet information, which not only helped to quantify the enhanced emissions at critical locations, but it also helped to define the emission source distribution of the disrupted steady flow for further dispersion modelling. The model then was applied to estimate particle number emissions at a bi-directional bus station used by diesel and compressed natural gas fuelled buses. It was found that the acceleration distance was of critical importance when estimating particle number emission, since the highest emissions occurred in sections where most of the buses were accelerating and no significant increases were observed at locations where they idled. It was also shown that emissions at the front end of the platform were 43 times greater than at the rear of the platform. Although the CLSE model is intended to be applied in traffic management and transport analysis systems for the evaluation of exposure, as well as the simulation of vehicle emissions in traffic interrupted microenvironments, the bus station model can also be used for the input of initial source definitions in future dispersion models.

  9. VOC emissions of Grey poplar leaves as affected by salt stress and different N sources.

    PubMed

    Teuber, M; Zimmer, I; Kreuzwieser, J; Ache, P; Polle, A; Rennenberg, H; Schnitzler, J-P

    2008-01-01

    Nitrogen nutrition and salt stress experiments were performed in a greenhouse with hydroponic-cultured, salt-sensitive Grey poplar (Populus x canescens) plants to study the combined influence of different N sources (either 1 mm NO(3) (-) or NH(4)(+)) and salt (up to 75 mm NaCl) on leaf gas exchange, isoprene biosynthesis and VOC emissions. Net assimilation and transpiration proved to be highly sensitive to salt stress and were reduced by approximately 90% at leaf sodium concentrations higher than 1,800 microg Na g dry weight (dw)(-1). In contrast, emissions of isoprene and oxygenated VOC (i.e. acetaldehyde, formaldehyde and acetone) were unaffected. There was no significant effect of combinations of salt stress and N source, and neither NO(3)(-) or NH(4)(+) influenced the salt stress response in the Grey poplar leaves. Also, transcript levels of 1-deoxy-d-xylulose 5-phosphate reductoisomerase (PcDXR) and isoprene synthase (PcISPS) did not respond to the different N sources and only responded slightly to salt application, although isoprene synthase (PcISPS) activity was negatively affected at least in one of two experiments, despite high isoprene emission rates. A significant salt effect was the strong reduction of leaf dimethylallyl diphosphate (DMADP) content, probably due to restricted availability of photosynthates for DMADP biosynthesis. Further consequences of reduced photosynthetic gas exchange and maintaining VOC emissions are a very high C loss, up to 50%, from VOC emissions related to net CO(2) uptake and a strong increase in leaf internal isoprene concentrations, with maximum mean values up to 6.6 microl x l(-1). Why poplar leaves maintain VOC biosynthesis and emission under salt stress conditions, despite impaired photosynthetic CO(2) fixation, is discussed.

  10. Extended H2 emission line sources from UWISH2

    NASA Astrophysics Data System (ADS)

    Froebrich, D.; Makin, S. V.; Davis, C. J.; Gledhill, T. M.; Kim, Y.; Koo, B.-C.; Rowles, J.; Eislöffel, J.; Nicholas, J.; Lee, J. J.; Williamson, J.; Buckner, A. S. M.

    2015-12-01

    We present the extended source catalogue for the UKIRT Wide Field Infrared Survey for H2 (UWISH2). The survey is unbiased along the inner Galactic Plane from l ≈ 357° to l ≈ 65° and |b| ≤ 1.5° and covers 209 deg2. A further 42.0 and 35.5 deg2 of high dust column density regions have been targeted in Cygnus and Auriga. We have identified 33 200 individual extended H2 features. They have been classified to be associated with about 700 groups of jets and outflows, 284 individual (candidate) planetary nebulae, 30 supernova remnants and about 1300 photodissociation regions. We find a clear decline of star formation activity (traced by H2 emission from jets and photodissociation regions) with increasing distance from the Galactic Centre. About 60 per cent of the detected candidate planetary nebulae have no known counterpart and 25 per cent of all supernova remnants have detectable H2 emission associated with them.

  11. 77 FR 26476 - Standards of Performance for Greenhouse Gas Emissions for New Stationary Sources: Electric...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-05-04

    ... AGENCY 40 CFR Part 60 Standards of Performance for Greenhouse Gas Emissions for New Stationary Sources... proposed rule, ``Standards of Performance for Greenhouse Gas Emissions for New Stationary Sources: Electric... for the proposed Standards of Performance for Greenhouse Gas Emissions for New Stationary...

  12. X-ray Emission from the Sombrero Galaxy: Discrete Sources

    NASA Astrophysics Data System (ADS)

    Li, Zhiyuan; Spitler, Lee R.; Jones, Christine; Forman, William R.; Kraft, Ralph P.; Di Stefano, Rosanne; Tang, Shikui; Wang, Q. Daniel; Gilfanov, Marat; Revnivtsev, Mikhail

    2010-10-01

    We present a study of discrete X-ray sources in and around the bulge-dominated, massive Sa galaxy, Sombrero (M104), based on new and archival Chandra observations with a total exposure of ~200 ks. With a detection limit of L X ≈ 1037 erg s-1 and a field of view covering a galactocentric radius of ~30 kpc (11farcm5), 383 sources are detected. Cross-correlation with Spitler et al.'s catalog of Sombrero globular clusters (GCs) identified from HST/ACS observations reveals 41 X-ray sources in GCs, presumably low-mass X-ray binaries (LMXBs). Metal-rich GCs are found to have a higher probability of hosting these LMXBs, a trend similar to that found in elliptical galaxies. On the other hand, the four most luminous GC LMXBs, with apparently super-Eddington luminosities for an accreting neutron star, are found in metal-poor GCs. We quantify the differential luminosity functions (LFs) for both the detected GC and field LMXBs, whose power-law indices (~1.1 for the GC-LF and ~1.6 for field-LF) are consistent with previous studies for elliptical galaxies. With precise sky positions of the GCs without a detected X-ray source, we further quantify, through a fluctuation analysis, the GC-LF at fainter luminosities down to 1035 erg s-1. The derived index rules out a faint-end slope flatter than 1.1 at a 2σ significance, contrary to recent findings in several elliptical galaxies and the bulge of M31. On the other hand, the 2-6 keV unresolved emission places a tight constraint on the field LF, implying a flattened index of ~1.0 below 1037 erg s-1. We also detect 101 sources in the halo of Sombrero. The presence of these sources cannot be interpreted as galactic LMXBs whose spatial distribution empirically follows the starlight. Their number is also higher than the expected number of cosmic active galactic nuclei (52 ± 11 [1σ]) whose surface density is constrained by deep X-ray surveys. We suggest that either the cosmic X-ray background is unusually high in the direction of

  13. High rates of anaerobic methane oxidation in freshwater wetlands reduce potential atmospheric methane emissions.

    PubMed

    Segarra, K E A; Schubotz, F; Samarkin, V; Yoshinaga, M Y; Hinrichs, K-U; Joye, S B

    2015-06-30

    The role of anaerobic oxidation of methane (AOM) in wetlands, the largest natural source of atmospheric methane, is poorly constrained. Here we report rates of microbially mediated AOM (average rate=20 nmol cm(-3) per day) in three freshwater wetlands that span multiple biogeographical provinces. The observed AOM rates rival those in marine environments. Most AOM activity may have been coupled to sulphate reduction, but other electron acceptors remain feasible. Lipid biomarkers typically associated with anaerobic methane-oxidizing archaea were more enriched in (13)C than those characteristic of marine systems, potentially due to distinct microbial metabolic pathways or dilution with heterotrophic isotope signals. On the basis of this extensive data set, AOM in freshwater wetlands may consume 200 Tg methane per year, reducing their potential methane emissions by over 50%. These findings challenge precepts surrounding wetland carbon cycling and demonstrate the environmental relevance of an anaerobic methane sink in ecosystems traditionally considered strong methane sources.

  14. Smog O3 Production Rate in California Air: Marker Compounds Allow Checks on Source Attribution to Fire and Other Sources

    NASA Astrophysics Data System (ADS)

    Chatfield, R. B.; Esswein, R. F.; Cai, C.; Kaduwela, A.; Kulkarni, S.; Blake, D. R.; Weinheimer, A. J.; Fried, A.; Huey, L. G.

    2012-12-01

    We are able to attribute sources of both radical reactivity and NO that determined the smog-chemical production rate of ozone, P(O3), for NASA's wide-ranging sampling of California air in June, 2008, part of the ARCTAS intensive. We relate formaldehyde, HCHO, and reactive nitrogen oxides, NOx, to a variety of distinct "marker" species that identify origins. We have labeled the sources and markers as (i) Fire emissions (CH3CN), (ii) Biogenic emissions (Isoprene), (iii) Urban/business emissions (CHCl3), (iv) Transport-related fuel consumption, (SO2), and (v) Refining/Port emissions ("residual" toluene). We use multiple linear regression with some appropriate restrictions. We achieve R-squared or explained variance of 88% for HCHO (VOC's) and 60% for NOx. HCHO and NOx are slowly evolving measures of potential ozone generation. The two related but radiation-influenced measures j (HCHO->H+HCO) x [HCHO] and [NO] quantitatively, but non-linearly, relate to instantaneous ozone production in California air, with R-squared of 86-93%, just as in New York City (Chatfield et al., Atmos. Environ., 2010). Maps of attribution for 650 samples from the Port of San Diego to the Northern Sierra foothills, and offshore -— all show huge variability in source attributions for VOCs and NOx. They indicate a widespread fire-emission influence on VOCs as they produce peroxy radicals, but show no positive influence on NOx, in fact consuming NOx from other sources. Comparisons with simulations help to refine our attribution classes and also to check balances of VOC emissions in available inventories. The use of the P(O3) measures is directly translatable to a method for estimate smog-ozone production rate from space, as data from another intensive, DISCOVER-AQ, show. (Left) A rare example where all sources contribute significantly, with markers and tentative attributions marked. (Right) Three different situations describing the control of smog ozone production, all from the same geographic

  15. Environmental tobacco smoke: mutagenic emission rates and their relationship to other emission factors

    SciTech Connect

    Lewtas, J.; Williams, K.; Lofroth, G.; Hammond, K.; Leaderer, B.

    1987-05-01

    The objective of this study was to evaluate the emission rates and exposure concentrations of mutagens, nicotine, and particles from cigarettes. Studies were conducted under controlled laboratory and chamber conditions as well as in personal residences. The mutagenicity of environmental tobacco smoke (ETS) was evaluated in three bioassays using two strains of Salmonella typhimurium. Strain TA98 was used in the standard plate-incorporation and microsuspension histidine reversion assays; and strain TM677 in a microsuspension forward mutation assay. The mutagenicity, expressed either per Ug particle or per Ug nicotine, appeared to be a relatively constant factor that did not vary significantly between various cigarette brands. These data are being used to model the emissions of mutagens to predict mutagenic exposure concentrations under various conditions.

  16. Quantifying Molecular Hydrogen Emissions and an Industrial Leakage Rate for the South Coast Air Basin of California

    NASA Astrophysics Data System (ADS)

    Irish, M. C.; Schroeder, J.; Beyersdorf, A. J.; Blake, D. R.

    2015-12-01

    The poorly understood atmospheric budget and distribution of molecular hydrogen (H2) have invited further research since the discovery that emissions from a hydrogen-based economy could have negative impacts on the global climate system and stratospheric ozone. The burgeoning fuel cell electric vehicle industry in the South Coast Air Basin of California (SoCAB) presents an opportunity to observe and constrain urban anthropogenic H2 emissions. This work presents the first H2 emissions estimate for the SoCAB and calculates an upper limit for the current rate of leakage from production and distribution infrastructure within the region. A top-down method utilized whole air samples collected during the Student Airborne Research Program (SARP) onboard the NASA DC-8 research aircraft from 23-25 June 2015 to estimate H2 emissions from combustion and non-combustion sources. H2:carbon monoxide (CO) and H2:carbon dioxide ratios from airborne observations were compared with experimentally established ratios from pure combustion source ratios and scaled with the well-constrained CO emissions inventory to yield H2 emissions of 24.9 ± 3.6 Gg a-1 (1σ) from combustion engines and 8.2 ± 4.7 Gg a-1 from non-combustion sources. Total daily production of H2 in the SoCAB was compared with the top-down results to estimate an upper limit leakage rate (5%) where all emissions not accounted for by incomplete combustion in engines were assumed to be emitted from H2 infrastructure. For bottom-up validation, the NOAA Hybrid Single Particle Lagrangian Integrated Trajectory dispersion model was run iteratively with all known stationary sources in attempt to constrain emissions. While this investigation determined that H2 emissions from non-combustion sources in the SoCAB are likely significant, more in-depth analysis is required to better predict the atmospheric implications of a hydrogen economy.

  17. Volatile organic compound emissions from unconventional natural gas production: Source signatures and air quality impacts

    NASA Astrophysics Data System (ADS)

    Swarthout, Robert F.

    Advances in horizontal drilling and hydraulic fracturing over the past two decades have allowed access to previously unrecoverable reservoirs of natural gas and led to an increase in natural gas production. Intensive unconventional natural gas extraction has led to concerns about impacts on air quality. Unconventional natural gas production has the potential to emit vast quantities of volatile organic compounds (VOCs) into the atmosphere. Many VOCs can be toxic, can produce ground-level ozone or secondary organic aerosols, and can impact climate. This dissertation presents the results of experiments designed to validate VOC measurement techniques, to quantify VOC emission rates from natural gas sources, to identify source signatures specific to natural gas emissions, and to quantify the impacts of these emissions on potential ozone formation and human health. Measurement campaigns were conducted in two natural gas production regions: the Denver-Julesburg Basin in northeast Colorado and the Marcellus Shale region surrounding Pittsburgh, Pennsylvania. An informal measurement intercomparison validated the canister sampling methodology used throughout this dissertation for the measurement of oxygenated VOCs. Mixing ratios of many VOCs measured during both campaigns were similar to or higher than those observed in polluted cities. Fluxes of natural gas-associated VOCs in Colorado ranged from 1.5-3 times industry estimates. Similar emission ratios relative to propane were observed for C2-C6 alkanes in both regions, and an isopentane:n-pentane ratio ≈1 was identified as a unique tracer for natural gas emissions. Source apportionment estimates indicated that natural gas emissions were responsible for the majority of C2-C8 alkanes observed in each region, but accounted for a small proportion of alkenes and aromatic compounds. Natural gas emissions in both regions accounted for approximately 20% of hydroxyl radical reactivity, which could hinder federal ozone standard

  18. VOC emission rates over London and South East England obtained by airborne eddy covariance.

    PubMed

    Vaughan, Adam R; Lee, James D; Shaw, Marvin D; Misztal, Pawel K; Metzger, Stefan; Vieno, Massimo; Davison, Brian; Karl, Thomas G; Carpenter, Lucy J; Lewis, Alastair C; Purvis, Ruth M; Goldstein, Allen H; Hewitt, C Nicholas

    2017-08-24

    Volatile organic compounds (VOCs) originate from a variety of sources, and play an intrinsic role in influencing air quality. Some VOCs, including benzene, are carcinogens and so directly affect human health, while others, such as isoprene, are very reactive in the atmosphere and play an important role in the formation of secondary pollutants such as ozone and particles. Here we report spatially-resolved measurements of the surface-to-atmosphere fluxes of VOCs across London and SE England made in 2013 and 2014. High-frequency 3-D wind velocities and VOC volume mixing ratios (made by proton transfer reaction - mass spectrometry) were obtained from a low-flying aircraft and used to calculate fluxes using the technique of eddy covariance. A footprint model was then used to quantify the flux contribution from the ground surface at spatial resolution of 100 m, averaged to 1 km. Measured fluxes of benzene over Greater London showed positive agreement with the UK's National Atmospheric Emissions Inventory, with the highest fluxes originating from central London. Comparison of MTBE and toluene fluxes suggest that petroleum evaporation is an important emission source of toluene in central London. Outside London, increased isoprene emissions were observed over wooded areas, at rates greater than those predicted by a UK regional application of the European Monitoring and Evaluation Programme model (EMEP4UK). This work demonstrates the applicability of the airborne eddy covariance method to the determination of anthropogenic and biogenic VOC fluxes and the possibility of validating emission inventories through measurements.

  19. Assessment of corrosion rate in prestressed concrete with acoustic emission

    NASA Astrophysics Data System (ADS)

    Mangual, Jesé; ElBatanouny, Mohamed K.; Vélez, William; Ziehl, Paul; Matta, Fabio; González, Miguel

    2011-04-01

    Acoustic Emission (AE) sensing was employed to assess the rate of corrosion of steel strands in small scale concrete block specimens. The corrosion process was accelerated in a laboratory environment using a potentiostat to supply a constant potential difference with a 3% NaCl solution as the electrolyte. The embedded prestressing steel strand served as the anode, and a copper plate served as the cathode. Corrosion rate, half-cell potential measurements, and AE activity were recorded continuously throughout each test and examined to assess the development of corrosion and its rate. At the end of each test the steel strands were cleaned and re-weighed to determine the mass loss and evaluate it vis-á-vis the AE data. The initiation and propagation phases of corrosion were correlated with the percentage mass loss of steel and the acquired AE signals. Results indicate that AE monitoring may be a useful aid in the detection and differentiation of the steel deterioration phases, and estimation of the locations of corroded areas.

  20. Emissions from Combustion of Open Area Sources: Prescribed Forest and Agricultural Burns

    EPA Science Inventory

    Emissions from wildfires and prescribed forest and agricultural burns generate a variety of emissions that can cause adverse health effects for humans, contribute to climate change, and decrease visibility. Only limited pollutant data are available for these sources, particularly...

  1. Next Generation Emission Measurements for Fugitive, Area Source, and Fence Line Applications?

    EPA Science Inventory

    Next generation emissions measurements (NGEM) is an EPA term for the rapidly advancing field of air pollutant sensor technologies, data integration concepts, and associated geospatial modeling strategies for source emissions measurements. Ranging from low coat sensors to satelli...

  2. Next Generation Emission Measurements for Fugitive, Area Source, and Fence Line Applications?

    EPA Science Inventory

    Next generation emissions measurements (NGEM) is an EPA term for the rapidly advancing field of air pollutant sensor technologies, data integration concepts, and associated geospatial modeling strategies for source emissions measurements. Ranging from low coat sensors to satelli...

  3. Emissions from Combustion of Open Area Sources: Prescribed Forest and Agricultural Burns

    EPA Science Inventory

    Emissions from wildfires and prescribed forest and agricultural burns generate a variety of emissions that can cause adverse health effects for humans, contribute to climate change, and decrease visibility. Only limited pollutant data are available for these sources, particularly...

  4. Simulating industrial emissions using atmospheric dispersion modeling system: model performance and source emission factors.

    PubMed

    El-Fadel, M; Abi-Esber, L

    2012-03-01

    In this paper, the Gaussian Atmospheric Dispersion Modeling System (ADMS4) was coupled with field observations of surface meteorology and concentrations of several air quality indicators (nitrogen oxides (NOx), carbon monoxide (CO), fine particulate matter (PM10) and sulfur dioxide (SO2)) to test the applicability of source emission factors set by the European Environment Agency (EEA) and the United States Environmental Protection Agency (USEPA) at an industrial complex. Best emission factors and data groupings based on receptor location, type of terrain and wind speed, were relied upon to examine model performance using statistical analyses of simulated and observed data. The model performance was deemed satisfactory for several scenarios when receptors were located at downwind sites with index of agreement 'd' values reaching 0.58, fractional bias 'FB' and geometric mean bias 'MG' values approaching 0 and 1, respectively, and normalized mean square error 'NMSE' values as low as 2.17. However, median ratios of predicted to observed concentrations 'Cp/Co' at variable downstream distances were 0.01, 0.36, 0.76 and 0.19 for NOx, CO, PM10 and SO2, respectively, and the fraction of predictions within a factor of two of observations 'FAC2' values were lower than 0.5, indicating that the model could not adequately replicate all observed variations in emittant concentrations. Also, the model was found to be significantly sensitive to the input emission factor bringing into light the deficiency in regulatory compliance modeling which often uses internationally reported emission factors without testing their applicability.

  5. Final LDRD report : enhanced spontaneous emission rate in visible III-nitride LEDs using 3D photonic crystal cavities.

    SciTech Connect

    Fischer, Arthur Joseph; Subramania, Ganapathi S.; Coley, Anthony J.; Lee, Yun-Ju; Li, Qiming; Wang, George T.; Luk, Ting Shan; Koleske, Daniel David; Fullmer, Kristine Wanta

    2009-09-01

    The fundamental spontaneous emission rate for a photon source can be modified by placing the emitter inside a periodic dielectric structure allowing the emission to be dramatically enhanced or suppressed depending on the intended application. We have investigated the relatively unexplored realm of interaction between semiconductor emitters and three dimensional photonic crystals in the visible spectrum. Although this interaction has been investigated at longer wavelengths, very little work has been done in the visible spectrum. During the course of this LDRD, we have fabricated TiO{sub 2} logpile photonic crystal structures with the shortest wavelength band gap ever demonstrated. A variety of different emitters with emission between 365 nm and 700 nm were incorporated into photonic crystal structures. Time-integrated and time-resolved photoluminescence measurements were performed to measure changes to the spontaneous emission rate. Both enhanced and suppressed emission were demonstrated and attributed to changes to the photonic density of states.

  6. Source limitation of carbon gas emissions in high-elevation mountain streams and lakes

    USGS Publications Warehouse

    Crawford, John T.; Dornblaser, Mark M.; Stanley, Emily H.; Clow, David W.; Striegl, Robert G.

    2015-01-01

    Inland waters are an important component of the global carbon cycle through transport, storage, and direct emissions of CO2 and CH4 to the atmosphere. Despite predictions of high physical gas exchange rates due to turbulent flows and ubiquitous supersaturation of CO2—and perhaps also CH4—patterns of gas emissions are essentially undocumented for high mountain ecosystems. Much like other headwater networks around the globe, we found that high-elevation streams in Rocky Mountain National Park, USA, were supersaturated with CO2 during the growing season and were net sources to the atmosphere. CO2concentrations in lakes, on the other hand, tended to be less than atmospheric equilibrium during the open water season. CO2 and CH4 emissions from the aquatic conduit were relatively small compared to many parts of the globe. Irrespective of the physical template for high gas exchange (high k), we found evidence of CO2 source limitation to mountain streams during the growing season, which limits overall CO2emissions. Our results suggest a reduced importance of aquatic ecosystems for carbon cycling in high-elevation landscapes having limited soil development and high CO2 consumption via mineral weathering.

  7. Source limitation of carbon gas emissions in high-elevation mountain streams and lakes

    NASA Astrophysics Data System (ADS)

    Crawford, John T.; Dornblaser, Mark M.; Stanley, Emily H.; Clow, David W.; Striegl, Robert G.

    2015-05-01

    Inland waters are an important component of the global carbon cycle through transport, storage, and direct emissions of CO2 and CH4 to the atmosphere. Despite predictions of high physical gas exchange rates due to turbulent flows and ubiquitous supersaturation of CO2—and perhaps also CH4—patterns of gas emissions are essentially undocumented for high mountain ecosystems. Much like other headwater networks around the globe, we found that high-elevation streams in Rocky Mountain National Park, USA, were supersaturated with CO2 during the growing season and were net sources to the atmosphere. CO2 concentrations in lakes, on the other hand, tended to be less than atmospheric equilibrium during the open water season. CO2 and CH4 emissions from the aquatic conduit were relatively small compared to many parts of the globe. Irrespective of the physical template for high gas exchange (high k), we found evidence of CO2 source limitation to mountain streams during the growing season, which limits overall CO2 emissions. Our results suggest a reduced importance of aquatic ecosystems for carbon cycling in high-elevation landscapes having limited soil development and high CO2 consumption via mineral weathering.

  8. HVAC SYSTEMS AS EMISSION SOURCES AFFECTING INDOOR AIR QUALITY: A CRITICAL REVIEW

    EPA Science Inventory

    The paper discusses results of an evaluation of literature on heating, ventilating, and air-conditioning (HVAC) systems as contaminant emission sources that affect indoor air quality (IAQ). The various literature sources and methods for characterizing HVAC emission sources are re...

  9. EMISSION FACTORS FOR IRON AND STEEL SOURCES: CRITERIA AND TOXIC POLLUTANTS

    EPA Science Inventory

    The report provides a comprehensive set of emission factors for sources of both criteria and toxic air pollutants in integrated iron and steel plants and specialty electric arc shops (minimills). Emission factors are identified for process sources, and process and open source fug...

  10. HVAC SYSTEMS AS EMISSION SOURCES AFFECTING INDOOR AIR QUALITY: A CRITICAL REVIEW

    EPA Science Inventory

    The paper discusses results of an evaluation of literature on heating, ventilating, and air-conditioning (HVAC) systems as contaminant emission sources that affect indoor air quality (IAQ). The various literature sources and methods for characterizing HVAC emission sources are re...

  11. 75 FR 522 - National Emission Standards for Hazardous Air Pollutants: Area Source Standards for Prepared...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-01-05

    ...EPA is issuing national emission standards for control of hazardous air pollutants (HAP) for the Prepared Feeds Manufacturing area source category. The emissions standards for new and existing sources are based on EPA's determination as to what constitutes the generally available control technology or management practices for the area source category.

  12. 40 CFR Table 1 to Subpart Dddddd... - Emission Limits and Standards for Existing Affected Sources

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... Existing Affected Sources 1 Table 1 to Subpart DDDDDD of Part 63 Protection of Environment ENVIRONMENTAL... Polyvinyl Chloride and Copolymers Production Area Sources Pt. 63, Subpt. DDDDDD, Table 1 Table 1 to Subpart DDDDDD of Part 63—Emission Limits and Standards for Existing Affected Sources For this type of emission...

  13. 40 CFR Table 2 to Subpart Qqqq of... - Emission Limits for Existing Affected Sources

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 12 2011-07-01 2009-07-01 true Emission Limits for Existing Affected... Affected Sources You must comply with the emission limits that apply to your affected source in the following table as required by § 63.4690. If the affected source applies coating to products in the...

  14. 40 CFR Table 2 to Subpart Qqqq of... - Emission Limits for Existing Affected Sources

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 13 2012-07-01 2012-07-01 false Emission Limits for Existing Affected... Existing Affected Sources You must comply with the emission limits that apply to your affected source in the following table as required by § 63.4690. If the affected source applies coating to products in...

  15. 40 CFR Table 2 to Subpart Qqqq of... - Emission Limits for Existing Affected Sources

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 13 2014-07-01 2014-07-01 false Emission Limits for Existing Affected... Existing Affected Sources You must comply with the emission limits that apply to your affected source in the following table as required by § 63.4690. If the affected source applies coating to products in...

  16. 40 CFR Table 2 to Subpart Kkkk of... - Emission Limits for Existing Affected Sources

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 13 2012-07-01 2012-07-01 false Emission Limits for Existing Affected Sources 2 Table 2 to Subpart KKKK of Part 63 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Affected Sources You must comply with the emission limits that apply to your affected source in the...

  17. 40 CFR 49.128 - Rule for limiting particulate matter emissions from wood products industry sources.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... emissions from wood products industry sources. 49.128 Section 49.128 Protection of Environment ENVIRONMENTAL... Region 10 § 49.128 Rule for limiting particulate matter emissions from wood products industry sources. (a... emitted from certain wood products industry sources operating within the Indian reservation to control...

  18. 40 CFR 49.128 - Rule for limiting particulate matter emissions from wood products industry sources.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... emissions from wood products industry sources. 49.128 Section 49.128 Protection of Environment ENVIRONMENTAL... Region 10 § 49.128 Rule for limiting particulate matter emissions from wood products industry sources. (a... emitted from certain wood products industry sources operating within the Indian reservation to control...

  19. 40 CFR 49.128 - Rule for limiting particulate matter emissions from wood products industry sources.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... emissions from wood products industry sources. 49.128 Section 49.128 Protection of Environment ENVIRONMENTAL... Region 10 § 49.128 Rule for limiting particulate matter emissions from wood products industry sources. (a... emitted from certain wood products industry sources operating within the Indian reservation to control...

  20. Reduced methane growth rate explained by decreased Northern Hemisphere microbial sources.

    PubMed

    Kai, Fuu Ming; Tyler, Stanley C; Randerson, James T; Blake, Donald R

    2011-08-10

    Atmospheric methane (CH(4)) increased through much of the twentieth century, but this trend gradually weakened until a stable state was temporarily reached around the turn of the millennium, after which levels increased once more. The reasons for the slowdown are incompletely understood, with past work identifying changes in fossil fuel, wetland and agricultural sources and hydroxyl (OH) sinks as important causal factors. Here we show that the late-twentieth-century changes in the CH(4) growth rates are best explained by reduced microbial sources in the Northern Hemisphere. Our results, based on synchronous time series of atmospheric CH(4) mixing and (13)C/(12)C ratios and a two-box atmospheric model, indicate that the evolution of the mixing ratio requires no significant change in Southern Hemisphere sources between 1984 and 2005. Observed changes in the interhemispheric difference of (13)C effectively exclude reduced fossil fuel emissions as the primary cause of the slowdown. The (13)C observations are consistent with long-term reductions in agricultural emissions or another microbial source within the Northern Hemisphere. Approximately half (51 ± 18%) of the decrease in Northern Hemisphere CH(4) emissions can be explained by reduced emissions from rice agriculture in Asia over the past three decades associated with increases in fertilizer application and reductions in water use.

  1. Characterization of helium/argon working gas systems in a radiofrequency glow discharge atomic emission source. Part I: Optical emission, sputtering and electrical characteristics

    NASA Astrophysics Data System (ADS)

    Christopher, Steven J.; Hartenstein, Matthew L.; Marcus, R. Kenneth; Belkin, Mikhail; Caruso, Joseph A.

    1998-08-01

    Studies are performed to determine the influence of discharge gas composition (helium/argon working gas mixtures) on the analyte emission signal intensities, sputtering rates, and DC-bias characteristics of an analytical radiofrequency glow discharge atomic emission spectroscopy (RF-GD-AES) source. As the partial pressure of He is increased from 0 to 15 torr, increased emission intensity is observed for a range of bulk and trace elements in NIST 1250 SRM (low alloy steel), regardless of the base pressure of Ar in the source (5 and 9 torr). In contrast to increases in analyte emission intensity of up to 300%, counterindicative decreases in the sputtering rates on the order of about 30-50% are observed. The magnitude of these effects depends on both the partial pressure of helium introduced to the source and the total pressure of the He and Ar gases. Use of relative emission yield (REY) to normalize changes in emission intensity to sputtering rates indicates that excitation efficiencies increase under these conditions. Increases in average electron energy and temperature appear to control this response. Decreases in both analyte emission intensities and sputter rates occur with increasing He partial pressure when the total pressure in the cell remains fixed (11 torr in these studies). Emission yields for the fixed pressure, mixed gas plasmas decrease as the partial pressure of He (He/Ar ratio) in the RF-GD source increases. In this case, decreases in electron number densities appear to dictate the lower REYs. Measurement of DC-bias values at the sample surface provide understanding with respect to the observed changes in sputtering rates as well as suggest the origins of changes in plasma electron energetics. Use of a diamond stylus profilometer provides both the quantitative sputter rate information as well as qualitative insights into the use of mixed gas plasmas for enhanced depth profiling capabilities. The analyte emission characteristics of these mixed gas

  2. Emission rates of sulfur dioxide, trace gases and metals from Mount Erebus, Antartica

    SciTech Connect

    Kyle, P.R.; Meeker, K. ); Finnegan, D. )

    1990-11-01

    SO{sub 2} emission rates have been measured annually since 1983 at Mount Erebus, Antarctica by correlation spectrometer (COSPEC V). Following a 4 month period of sustained strombolian activity in late 1984, SO{sub 2} emissions declined from 230 Mg/day in 1983 to 25 Mg/day and then slowly increased from 16 Mg/day in 1985 to 51 Mg/day in 1987. Nine sets of filter packs containing partcle and {sup 7}LiOH treated filters were collected in the plume in 1986 and analyzed by neutron activation. Using the COSPEC data and measured element/S ratios on the filters, emission rates have been determined for trace gases and metals. The authors infer HCl and HF emissions in 1983 to be about 1200 and 500 Mg/day, respectively. Mt Erebus has therefore been an important source of halogens to the Anarctic atmosphere and could be responsible for excess Cl found in Central Antarctica snow.

  3. Models and statistical methods for gaseous-emission testing of finite sources in well-mixed chambers

    SciTech Connect

    Dunn, J.E.

    1987-01-01

    This paper proposes two families of mathematical models to represent either the concentration of a gaseous emission in (or the accumulated amount exiting from) a well-mixed, environmentally controlled test chamber. A thin-film model, which seems applicable to such sources as carpet adhesive, has the capability of isolating the true emission rate constant from chamber effects. It has successfully modeled emissions of methyl ethyl ketone, a C8 alcohol, and butyl propionate from latex caulk. Chamber effects in the form of temporary wall retention were identified for the latter two compounds. An analogous, deep source, diffusion-limited model for plywood, etc., once fitted to a data set, can be used to generalize to other combinations of source surface area, chamber volume, and air exchange rate.

  4. Impact of source-production revision on the dose-rate constant of {sup 131}Cs interstitial brachytherapy sources

    SciTech Connect

    Chen Zhe; Bongiorni, Paul; Nath, Ravinder

    2010-07-15

    Purpose: Since its introduction in 2004, the model CS-1 Rev.1 {sup 131}Cs source has been used in many radiation therapy clinics for prostate brachytherapy. In 2006, this source model underwent a Rev.2 production revision. The aim of this work was to investigate the dosimetric influences of the Rev.2 production revision using high-resolution photon spectrometry. Methods: Three CS-1 Rev.1 and three CS-1 Rev.2 {sup 131}Cs sources were used in this study. The relative photon energy spectrum emitted by each source in the transverse bisector of the source was measured using a high-resolution germanium detector designed for low-energy photon spectrometry. Based on the measured photon energy spectrum and the radioactivity distribution in the source, the dose-rate constant ({Lambda}) of each source was determined. The effects of the Rev.2 production revision were quantified by comparing the emitted photon energy spectra and the {Lambda} values determined for the sources manufactured before and after the production revision. Results: The relative photon energy spectrum originating from the principal emissions of {sup 131}Cs was found to be nearly identical before and after the Rev.2 revision. However, the portion of the spectrum originating from the production of fluorescent x rays in niobium, a trace element present in the source construction materials, was found to differ significantly between the Rev.1 and Rev.2 sources. The peak intensity of the Nb K{sub {alpha}} and Nb K{sub {beta}} fluorescent x rays from the Rev.2 source was approximately 35% of that from the Rev.1 source. Consequently, the nominal {Lambda} value of the Rev.2 source was found to be greater than that determined for the Rev.1 source by approximately 0.7%{+-}0.5%. Conclusions: A significant reduction (65%) in relative niobium fluorescent x-ray yield was observed in the Rev.2 {sup 131}Cs sources. The impact of this reduction on the dose-rate constant was found to be small, with a relative difference of

  5. Indoor acrolein emission and decay rates resulting from domestic cooking events

    NASA Astrophysics Data System (ADS)

    Seaman, Vincent Y.; Bennett, Deborah H.; Cahill, Thomas M.

    2009-12-01

    Acrolein (2-propenal) is a common constituent of both indoor and outdoor air, can exacerbate asthma in children, and may contribute to other chronic lung diseases. Recent studies have found high indoor levels of acrolein and other carbonyls compared to outdoor ambient concentrations. Heated cooking oils produce considerable amounts of acrolein, thus cooking is likely an important source of indoor acrolein. A series of cooking experiments were conducted to determine the emission rates of acrolein and other volatile carbonyls for different types of cooking oils (canola, soybean, corn and olive oils) and deep-frying different food items. Similar concentrations and emission rates of carbonyls were found when different vegetable oils were used to deep-fry the same food product. The food item being deep-fried was generally not a significant source of carbonyls compared to the cooking oil. The oil cooking events resulted in high concentrations of acrolein that were in the range of 26.4-64.5 μg m -3. These concentrations exceed all the chronic regulatory exposure limits and many of the acute exposure limits. The air exchange rate and the decay rate of the carbonyls were monitored to estimate the half-life of the carbonyls. The half-life for acrolein was 14.4 ± 2.6 h, which indicates that indoor acrolein concentrations can persist for considerable time after cooking in poorly-ventilated homes.

  6. A short pulse, high rep-rate microdischarge VUV source

    NASA Astrophysics Data System (ADS)

    Stephens, Jacob; Fierro, Andrew; Dickens, James; Neuber, Andreas; CenterPulsed Power; Power Electronics Team

    2013-09-01

    A MOSFET based high voltage pulser is utilized to excite a microdischarge (MD), or microdischarge array (MDA) with pulsed voltages of up to 1 kV, with risetime and FWHM on the order of 10 ns and 30 ns, respectively. Additionally, the pulser is capable of pulsing at rep-rates in excess of 35 MHz. However, for these experiments the rep-rate was set on the order of 1 MHz, so as to limit excess energy deposition into the background gas and optimize the energy efficiency of VUV generation. Using VUV capable spectral diagnostics, the VUV emission of the MDs for various pressures (50-800 + Torr) and gases, focused on argon, argon-hydrogen mixtures, and neon-hydrogen mixtures (all of which provide strong emission at λ < 130 nm) is studied, for pulsed, MHz rep-rated excitation. Using a photomultiplier tube the time dependent behavior of the VUV emission is characterized and compared to results from transient fluid modeling of the MDA. For instance, the MDA turn-on time is recorded to be about 15 ns, which matches the full plasma development time in the model, and the MDA self- capacitance largely determines the turn-off behavior. This research was supported by an AFOSR grant on the Physics of Distributed Plasma Discharges and fellowships from the National Physical Sciences Consortium, supported by Sandia National Laboratories.

  7. A Global Catalogue of Large SO2 Sources and Emissions Derived from the Ozone Monitoring Instrument

    NASA Technical Reports Server (NTRS)

    Fioletov, Vitali E.; McLinden, Chris A.; Krotkov, Nickolay; Li, Can; Joiner, Joanna; Theys, Nicolas; Carn, Simon; Moran, Mike D.

    2016-01-01

    Sulfur dioxide (SO2) measurements from the Ozone Monitoring Instrument (OMI) satellite sensor processed with the new principal component analysis (PCA) algorithm were used to detect large point emission sources or clusters of sources. The total of 491 continuously emitting point sources releasing from about 30 kt yr(exp -1) to more than 4000 kt yr(exp -1) of SO2 per year have been identified and grouped by country and by primary source origin: volcanoes (76 sources); power plants (297); smelters (53); and sources related to the oil and gas industry (65). The sources were identified using different methods, including through OMI measurements themselves applied to a new emission detection algorithm, and their evolution during the 2005- 2014 period was traced by estimating annual emissions from each source. For volcanic sources, the study focused on continuous degassing, and emissions from explosive eruptions were excluded. Emissions from degassing volcanic sources were measured, many for the first time, and collectively they account for about 30% of total SO2 emissions estimated from OMI measurements, but that fraction has increased in recent years given that cumulative global emissions from power plants and smelters are declining while emissions from oil and gas industry remained nearly constant. Anthropogenic emissions from the USA declined by 80% over the 2005-2014 period as did emissions from western and central Europe, whereas emissions from India nearly doubled, and emissions from other large SO2-emitting regions (South Africa, Russia, Mexico, and the Middle East) remained fairly constant. In total, OMI-based estimates account for about a half of total reported anthropogenic SO2 emissions; the remaining half is likely related to sources emitting less than 30 kt yr(exp -1) and not detected by OMI.

  8. A Global Catalogue of Large SO2 Sources and Emissions Derived from the Ozone Monitoring Instrument

    NASA Technical Reports Server (NTRS)

    Fioletov, Vitali E.; McLinden, Chris A.; Krotkov, Nickolay; Li, Can; Joiner, Joanna; Theys, Nicolas; Carn, Simon; Moran, Mike D.

    2016-01-01

    Sulfur dioxide (SO2) measurements from the Ozone Monitoring Instrument (OMI) satellite sensor processed with the new principal component analysis (PCA) algorithm were used to detect large point emission sources or clusters of sources. The total of 491 continuously emitting point sources releasing from about 30 kt yr(exp -1) to more than 4000 kt yr(exp -1) of SO2 per year have been identified and grouped by country and by primary source origin: volcanoes (76 sources); power plants (297); smelters (53); and sources related to the oil and gas industry (65). The sources were identified using different methods, including through OMI measurements themselves applied to a new emission detection algorithm, and their evolution during the 2005- 2014 period was traced by estimating annual emissions from each source. For volcanic sources, the study focused on continuous degassing, and emissions from explosive eruptions were excluded. Emissions from degassing volcanic sources were measured, many for the first time, and collectively they account for about 30% of total SO2 emissions estimated from OMI measurements, but that fraction has increased in recent years given that cumulative global emissions from power plants and smelters are declining while emissions from oil and gas industry remained nearly constant. Anthropogenic emissions from the USA declined by 80% over the 2005-2014 period as did emissions from western and central Europe, whereas emissions from India nearly doubled, and emissions from other large SO2-emitting regions (South Africa, Russia, Mexico, and the Middle East) remained fairly constant. In total, OMI-based estimates account for about a half of total reported anthropogenic SO2 emissions; the remaining half is likely related to sources emitting less than 30 kt yr(exp -1) and not detected by OMI.

  9. A global catalogue of large SO2 sources and emissions derived from the Ozone Monitoring Instrument

    NASA Astrophysics Data System (ADS)

    Fioletov, Vitali E.; McLinden, Chris A.; Krotkov, Nickolay; Li, Can; Joiner, Joanna; Theys, Nicolas; Carn, Simon; Moran, Mike D.

    2016-09-01

    Sulfur dioxide (SO2) measurements from the Ozone Monitoring Instrument (OMI) satellite sensor processed with the new principal component analysis (PCA) algorithm were used to detect large point emission sources or clusters of sources. The total of 491 continuously emitting point sources releasing from about 30 kt yr-1 to more than 4000 kt yr-1 of SO2 per year have been identified and grouped by country and by primary source origin: volcanoes (76 sources); power plants (297); smelters (53); and sources related to the oil and gas industry (65). The sources were identified using different methods, including through OMI measurements themselves applied to a new emission detection algorithm, and their evolution during the 2005-2014 period was traced by estimating annual emissions from each source. For volcanic sources, the study focused on continuous degassing, and emissions from explosive eruptions were excluded. Emissions from degassing volcanic sources were measured, many for the first time, and collectively they account for about 30 % of total SO2 emissions estimated from OMI measurements, but that fraction has increased in recent years given that cumulative global emissions from power plants and smelters are declining while emissions from oil and gas industry remained nearly constant. Anthropogenic emissions from the USA declined by 80 % over the 2005-2014 period as did emissions from western and central Europe, whereas emissions from India nearly doubled, and emissions from other large SO2-emitting regions (South Africa, Russia, Mexico, and the Middle East) remained fairly constant. In total, OMI-based estimates account for about a half of total reported anthropogenic SO2 emissions; the remaining half is likely related to sources emitting less than 30 kt yr-1 and not detected by OMI.

  10. 76 FR 15553 - National Emission Standards for Hazardous Air Pollutants for Area Sources: Industrial, Commercial...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-21

    ...EPA is promulgating national emission standards for control of hazardous air pollutants from two area source categories: Industrial boilers and commercial and institutional boilers. The final emission standards for control of mercury and polycyclic organic matter emissions from coal-fired area source boilers are based on the maximum achievable control technology. The final emission standards for control of hazardous air pollutants emissions from biomass-fired and oil-fired area source boilers are based on EPA's determination as to what constitutes the generally available control technology or management practices.

  11. Standard formaldehyde source for chamber testing of material emissions: model development, experimental evaluation, and impacts of environmental factors.

    PubMed

    Wei, Wenjuan; Howard-Reed, Cynthia; Persily, Andrew; Zhang, Yinping

    2013-07-16

    Formaldehyde, which is recognized as a harmful indoor air pollutant for human health, is emitted mainly from urea-formaldehyde resin in wood products. Chamber tests are used to evaluate formaldehyde emission rates from these products. However, there is no available formaldehyde standard reference emission source to assess the performance of chamber testing systems. In this work, a LIFE (liquid-inner tube diffusion-film-emission) formaldehyde reference is described. The formaldehyde source consists of a polytetrafluoroethene (PTFE) tube that holds a formaldehyde-water solution with a concentration of 16 g formaldehyde per 100 mL water, with a thin polydimethylsiloxane (PDMS) film cover. Formaldehyde emission parameters for the PDMS film (diffusion coefficient and partition coefficient) were determined experimentally, thereby enabling the prediction of the formaldehyde emissions from the source for use as a reference value in a chamber. Chamber tests were conducted in a 51 L stainless steel ventilated chamber. The impacts of temperature and relative humidity on the emissions were investigated. Results show the LIFE's chamber test results match those predicted by a mass transfer model. As a result, this formaldehyde source may be used to generate a reference concentration in product emission testing chambers, thereby providing a powerful tool to evaluate the performance of the chamber testing systems.

  12. Impact of routine episodic emissions on the expected frequency distribution of emissions from oil and gas production sources.

    NASA Astrophysics Data System (ADS)

    Smith, N.; Blewitt, D.; Hebert, L. B.

    2015-12-01

    In coordination with oil and gas operators, we developed a high resolution (< 1 min) simulation of temporal variability in well-pad oil and gas emissions over a year. We include routine emissions from condensate tanks, dehydrators, pneumatic devices, fugitive leaks and liquids unloading. We explore the variability in natural gas emissions from these individual well-pad sources, and find that routine short-term episodic emissions such as tank flashing and liquids unloading result in the appearance of a skewed, or 'fat-tail' distribution of emissions, from an individual well-pad over time. Additionally, we explore the expected variability in emissions from multiple wells with different raw gas composition, gas/liquids production volumes and control equipment. Differences in well-level composition, production volume and control equipment translate into differences in well-level emissions leading to a fat-tail distribution of emissions in the absence of operational upsets. Our results have several implications for recent studies focusing on emissions from oil and gas sources. Time scale of emission estimates are important and have important policy implications. Fat tail distributions may not be entirely driven by avoidable mechanical failures, and are expected to occur under routine operational conditions from short-duration emissions (e.g., tank flashing, liquid unloading). An understanding of the expected distribution of emissions for a particular population of wells is necessary to evaluate whether the observed distribution is more skewed than expected. Temporal variability in well-pad emissions make comparisons to annual average emissions inventories difficult and may complicate the interpretation of long-term ambient fenceline monitoring data. Sophisticated change detection algorithms will be necessary to identify when true operational upsets occur versus routine short-term emissions.

  13. Emission of volatile organic compounds from silage: Compounds, sources, and implications

    NASA Astrophysics Data System (ADS)

    Hafner, Sasha D.; Howard, Cody; Muck, Richard E.; Franco, Roberta B.; Montes, Felipe; Green, Peter G.; Mitloehner, Frank; Trabue, Steven L.; Rotz, C. Alan

    2013-10-01

    Silage, fermented cattle feed, has recently been identified as a significant source of volatile organic compounds (VOCs) to the atmosphere. A small number of studies have measured VOC emission from silage, but not enough is known about the processes involved to accurately quantify emission rates and identify practices that could reduce emissions. Through a literature review, we have focused on identifying the most important compounds emitted from corn silage (the most common type of silage in the US) and the sources of these compounds by quantifying their production and emission potential in silage and describing production pathways. We reviewed measurements of VOC emission from silage and assessed the importance of individual silage VOCs through a quantitative analysis of VOC concentrations within silage. Measurements of VOC emission from silage and VOCs present within silage indicated that alcohols generally make the largest contribution to emission from corn silage, in terms of mass emitted and potential ozone formation. Ethanol is the dominant alcohol in corn silage; excluding acids, it makes up more than half of the mean mass of VOCs present. Acids, primarily acetic acid, may be important when emission is high and all VOCs are nearly depleted by emission. Aldehydes and esters, which are more volatile than acids and alcohols, are important when exposure is short, limiting emission of more abundant but less volatile compounds. Variability in silage VOC concentrations is very high; for most alcohols and acids, tolerance intervals indicate that 25% of silages have concentrations a factor of two away from median values, and possibly much further. This observation suggests that management practices can significantly influence VOC concentrations. Variability also makes prediction of emissions difficult. The most important acids, alcohols, and aldehydes present in silage are probably produced by bacteria (and, in the case of ethanol, yeasts) during fermentation and

  14. Source location of the smooth high-frequency radio emissions from Uranus

    NASA Technical Reports Server (NTRS)

    Farrell, W. M.; Calvert, W.

    1989-01-01

    The source location of the smooth high-frequency radio emissions from Uranus has been determined. Specifically, by fitting the signal dropouts which occurred as Voyager traversed the hollow center of the emission pattern to a symmetrical cone centered on the source magnetic field direction at the cyclotron frequency, a southern-hemisphere (nightside) source was found at approximately 56 deg S, 219 deg W. The half-angle for the hollow portion of the emission pattern was found to be 13 deg.

  15. The nuclear region of low luminosity flat radio spectrum sources. II. Emission-line spectra

    NASA Astrophysics Data System (ADS)

    Gonçalves, A. C.; Serote Roos, M.

    2004-01-01

    We report on the spectroscopic study of 19 low luminosity Flat Radio Spectrum (LL FRS) sources selected from Marchã's et al. (\\cite{March96}) 200 mJy sample. In the optical, these objects are mainly dominated by the host galaxy starlight. After correcting the data for this effect, we obtain a new set of spectra clearly displaying weak emission lines; such features carry valuable information concerning the excitation mechanisms at work in the nuclear regions of LL FRS sources. We have used a special routine to model the spectra and assess the intensities and velocities of the emission lines; we have analyzed the results in terms of diagnostic diagrams. Our analysis shows that 79% of the studied objects harbour a Low Ionization Nuclear Emission-line Region (or LINER) whose contribution was swamped by the host galaxy starlight. The remaining objects display a higher ionization spectrum, more typical of Seyferts; due to the poor quality of the spectra, it was not possible to identify any possible large Balmer components. The fact that we observe a LINER-type spectrum in LL FRS sources supports the idea that some of these objects could be undergoing an ADAF phase; in addition, such a low ionization emission-line spectrum is in agreement with the black hole mass values and sub-Eddington accretion rates published for some FRS sources. Based on observations collected at the Multiple Mirror Telescope on Mt. Hopkins. Full Fig. 1 is only available in electronic form at http://www.edpsciences.org

  16. Joint source-channel rate allocation in parallel channels.

    PubMed

    Pu, Lingling; Marcellin, Michael W; Djordjevic, Ivan; Vasic, Bane; Bilgin, Ali

    2007-08-01

    A fast rate-optimal rate allocation algorithm is proposed for parallel transmission of scalable images in multichannel systems. Scalable images are transmitted via fixed-length packets. The proposed algorithm selects a subchannel, as well as a channel code rate for each packet, based on the signal-to-noise ratios (SNRs) of the subchannels. The resulting scheme provides unequal error protection of source bits and significant gains are obtained over equal error protection schemes. An application of the proposed algorithm to JPEG2000 transmission shows the advantages of exploiting differences in SNRs between subchannels. Multiplexing of multiple sources is also considered, and additional gains are achieved by exploiting information diversity among the sources.

  17. Global sources of non-CO2 greenhouse gas emissions: regional trends, uncertainties and options for emission reductions

    NASA Astrophysics Data System (ADS)

    Olivier, J. G.; van Aardenne, J. A.; Peters, J. A.

    2005-05-01

    An overview will be presented of sources and trends of global emissions of direct non-CO2 greenhouse gases CH4, N2O and the fluorinated gases HFCs, PFCs and SF6, which are addressed in the Kyoto protocol. Special attention will be given to regional source trends, estimated uncertainties and most recent global emission trends. In addition, the most significant options for emission reductions will be discussed in view of medium term emission scenarios that were meant to illustrate future trends without the effects climate policy. For estimating the recent global emission trends a special approach was used to compile fast annual updates of the EDGAR global emission inventories, based on the more detailed previous version. We present an overview of the approaches used for this `Fast Track' for the different source sectors. Results are presented for 1995-2002 for various anthropogenic sources at regional scales including an estimate of the accuracies achieved. A similar overview will be provided for the emissions of the ozone precursors NOx, CO and NMVOC and of black carbon. Tropospheric ozone and black carbon are both greenhouse gases, which are not considered in the Kyoto protocol, but in industrialised countries the emissions that cause them are often part of environmental policy on local and regional air quality.

  18. A model to relate wind tunnel measurements to open field odorant emissions from liquid area sources

    NASA Astrophysics Data System (ADS)

    Lucernoni, F.; Capelli, L.; Busini, V.; Sironi, S.

    2017-05-01

    Waste Water Treatment Plants are known to have significant emissions of several pollutants and odorants causing nuisance to the near-living population. One of the purposes of the present work is to study a suitable model to evaluate odour emissions from liquid passive area sources. First, the models describing volatilization under a forced convection regime inside a wind tunnel device, which is the sampling device that typically used for sampling on liquid area sources, were investigated. In order to relate the fluid dynamic conditions inside the hood to the open field and inside the hood a thorough study of the models capable of describing the volatilization phenomena of the odorous compounds from liquid pools was performed and several different models were evaluated for the open field emission. By means of experimental tests involving pure liquid acetone and pure liquid butanone, it was verified that the model more suitable to describe precisely the volatilization inside the sampling hood is the model for the emission from a single flat plate in forced convection and laminar regime, with a fluid dynamic boundary layer fully developed and a mass transfer boundary layer not fully developed. The proportionality coefficient for the model was re-evaluated in order to account for the specific characteristics of the adopted wind tunnel device, and then the model was related with the selected model for the open field thereby computing the wind speed at 10 m that would cause the same emission that is estimated from the wind tunnel measurement furthermore, the field of application of the proposed model was clearly defined for the considered models during the project, discussing the two different kinds of compounds commonly found in emissive liquid pools or liquid spills, i.e. gas phase controlled and liquid phase controlled compounds. Lastly, a discussion is presented comparing the presented approach for emission rates recalculation in the field, with other approaches

  19. A waveguide electron cyclotron resonance source of X-ray emission for low-dose introscopy

    NASA Astrophysics Data System (ADS)

    Sergeichev, K. F.; Ionidi, V. Yu.; Karfidov, D. M.; Lukina, N. A.

    2013-12-01

    It is shown that a "point" target in a conventional evacuated waveguide in the magnetic field of a mirror trap formed by two disk magnets axially magnetized in the direction perpendicular to the electric field vector represents a source of X-ray bremsstrahlung of electrons accelerated in an ECR discharge with a broad range of photon energies up to 0.8 MeV. The dosage rate of the source is ˜1 R/h. The source fed from a conventional microwave oven has small dimensions and a low weight. It is easy-to-use and is suitable as a laboratory tool, in particular, in radiobiology and introscopy. After passing through the object, X-ray emission is recorded by a digital camera with the help of a highly sensitive X-ray fluorescent screen, which converts it into an optical image.

  20. Evaluation of PM 10 emission rates from paved and unpaved roads using tracer techniques

    NASA Astrophysics Data System (ADS)

    Claiborn, Candis; Mitra, Arundhati; Adams, Glenn; Bamesberger, Lee; Allwine, Gene; Kantamaneni, Ravi; Lamb, Brian; Westberg, Hal

    Spokane, WA, is a nonattainment area for airborne particulate matter smaller than 10μm (PM 10), so that a detailed emission inventory for PM 10 is needed to evaluate various control strategies. It is thought that emissions from paved and unpaved roads in Spokane contribute three-fourths of the anthropogenic PM 10 (neglecting wind-blown dust from agricultural areas). A study was conducted in the summer and fall of 1992 and again in the spring and summer of 1994 to measure PM 10 emission rates from paved and unpaved roads in Eastern Washington state using a novel tracer technique. A known amount of an inert tracer (SF 6) was released and concentrations of PM 10 and SF 6 downwind of the road, along with meteorological parameters and traffic volume, were measured. The results of the tracer experiments showed that within experimental uncertainties the PM 10 and the tracer gas disperse in the same manner, suggesting that the use of a tracer in a line source to simulate roadway PM 10 emissions can provide a tool for improving the existing emission inventories from roads. The emission factors obtained from two unpaved road experiments (136 g per vehicle per kilometer traveled, or g VKT -1, and 336 g VKT -1) were similar in magnitude to those predicted using currently accepted empirical algorithms. The factors determined from six paved road experiments were approximately 80% higher than that predicted using current formulae (6.7 ± 3.7 g VKT -1 compared to 3.7 g VKT -1) for two-lane roads with daily traffic less than 10,000 vehicles. For major highways (4 + lanes and traffic in excess of 10,000 vehicles per day) the emission factors obtained from the tracer experiments were, on average, 44% lower than those predicted using standard formulae (1.0 ± 0.5 g VKT -1 compared to 1.8 g VKT -1). The calculated emission factors for paved roads exhibited a wide range of variability, suggesting that in order to quantify PM 10 emission rates from paved roads, more investigation is

  1. Sequential multi-nuclide emission rate estimation method based on gamma dose rate measurement for nuclear emergency management.

    PubMed

    Zhang, Xiaole; Raskob, Wolfgang; Landman, Claudia; Trybushnyi, Dmytro; Li, Yu

    2017-03-05

    In case of a nuclear accident, the source term is typically not known but extremely important for the assessment of the consequences to the affected population. Therefore the assessment of the potential source term is of uppermost importance for emergency response. A fully sequential method, derived from a regularized weighted least square problem, is proposed to reconstruct the emission and composition of a multiple-nuclide release using gamma dose rate measurement. The a priori nuclide ratios are incorporated into the background error covariance (BEC) matrix, which is dynamically augmented and sequentially updated. The negative estimations in the mathematical algorithm are suppressed by utilizing artificial zero-observations (with large uncertainties) to simultaneously update the state vector and BEC. The method is evaluated by twin experiments based on the JRodos system. The results indicate that the new method successfully reconstructs the emission and its uncertainties. Accurate a priori ratio accelerates the analysis process, which obtains satisfactory results with only limited number of measurements, otherwise it needs more measurements to generate reasonable estimations. The suppression of negative estimation effectively improves the performance, especially for the situation with poor a priori information, where it is more prone to the generation of negative values. Copyright © 2016 Elsevier B.V. All rights reserved.

  2. Source fingerprint monitoring of air pollutants from petrochemical industry and the determination of their annual emission flux using open path Fourier transform infrared spectroscopy

    SciTech Connect

    Yih-Shiaw Huang; Shih-Yi Chang; Tai-Ly Tso

    1996-12-31

    Toxic air pollutants were investigated in several petrochemical industrial park in Taiwan using a movable open-path Fourier-transform infrared spectroscopy (FTIR). The results show the qualitative and quantitative analysis of emission gases from plants, and also provide the emission rates of various compounds. More than twenty compounds under usual operation were found from these industrial park. The concentration variation with time could be correlated exactly with the distances from the emission source along the wind direction. This means that by changing the measuring points the source of emission could be unambiguously identified. The point, area and line source (PAL) plume dispersion model has been applied to estimate the emission rate of either a point or an area source. The local atmospheric stability was determined by releasing an SF{sub 6} tracer. The origin of errors came mainly from the uncertainty of the source configuration and the variation of the meteorological condition. Through continuous measurement using a portable open-path Fourier transform infrared (POP-FTIR) spectrometer, the maximum value of the emission rate and the annual amount of emission could be derived. The emission rate of the measured toxic gases was derived by the model technique, and the results show that the emission amount is on the order of ten to hundred tons per year.

  3. Sources of variability in distortion product otoacoustic emissions

    PubMed Central

    Garner, Cassie A.; Neely, Stephen T.; Gorga, Michael P.

    2008-01-01

    The goal of this study was to determine the extent to which the variability seen in distortion product otoacoustic emissions (DPOAEs), among ears with normal hearing, could be accounted for. Several factors were selected for investigation, including behavioral threshold, differences in middle-ear transmission characteristics either in the forward or the reverse direction, and differences in contributions from the distortion and reflection sources. These variables were assessed after optimizing stimulus parameters for individual ears at each frequency. A multiple-linear regression was performed to identify whether the selected variables, either individually or in combination, explained significant portions of variability in DPOAE responses. Behavioral threshold at the f2 frequency and behavioral threshold squared at that same frequency explained the largest amount of variability in DPOAE level, compared to the other variables. The combined model explained a small, but significant, amount of variance in DPOAE level at five frequencies. A large amount of residual variability remained, even at frequencies where the model accounted for significant amounts of variance. PMID:18681596

  4. Modelling the NO emissions from wildfires at the source level

    NASA Astrophysics Data System (ADS)

    Pérez-Ramirez, Y.; Santoni, P.-A.; Darabiha, N.

    2014-05-01

    There is a growing interest to characterize fire plumes in order to control air quality during wildfire episodes and to estimate the carbon and ozone balance of fire emissions. A numerical approach has been used to study the mechanisms of NO formation at the source level in wildfires given that NO plays an important role in the formation of ground-level ozone. The major reaction mechanisms involved in NO chemistry have been identified using reaction path analysis. Accordingly, a two-step global kinetic scheme in the gas phase has been proposed herein to account for the volatile fuel-bound nitrogen (fuel-N) conversion to NO, considering that the volatile fraction of fuel-N is released as NH3. Data from simulations using the perfectly stirred reactor (PSR) code from CHEMKIN-II package with a detailed kinetic mechanism (GDF-Kin® 3.0) have been used to calibrate and evaluate the global model under typical wildfire conditions in terms of the composition of the degradation gases of vegetation, the equivalence ratio, the range of temperatures and the residence time.

  5. COMBINING RATE-BASED AND CAP-AND-TRADE EMISSIONS POLICIES. (R828628)

    EPA Science Inventory

    Rate-based emissions policies (like tradable performance standards, TPS) fix average emissions intensity, while cap-and-trade (CAT) policies fix total emissions. This paper shows that unfettered trade between rate-based and cap-and-trade programs always raises combined emissio...

  6. Exhaust Emission Rates for Heavy-Duty Onroad Vehicles in the Next Version of MOVES

    EPA Science Inventory

    Derivation of the exhaust and crankcase emission rates for HC, CO, NOx, and PM emissions from medium and heavy-duty diesel, gasoline, and compressed natural gas vehicles. Including updates for emission rates for 2007 and later model year diesel vehicles

  7. COMBINING RATE-BASED AND CAP-AND-TRADE EMISSIONS POLICIES. (R828628)

    EPA Science Inventory

    Rate-based emissions policies (like tradable performance standards, TPS) fix average emissions intensity, while cap-and-trade (CAT) policies fix total emissions. This paper shows that unfettered trade between rate-based and cap-and-trade programs always raises combined emissio...

  8. Exhaust Emission Rates for Heavy-Duty Onroad Vehicles in the Next Version of MOVES

    EPA Science Inventory

    Derivation of the exhaust and crankcase emission rates for HC, CO, NOx, and PM emissions from medium and heavy-duty diesel, gasoline, and compressed natural gas vehicles. Including updates for emission rates for 2007 and later model year diesel vehicles

  9. Nine years of global hydrocarbon emissions based on source inversion of OMI formaldehyde observations

    NASA Astrophysics Data System (ADS)

    Bauwens, Maite; Stavrakou, Trissevgeni; Müller, Jean-François; De Smedt, Isabelle; Van Roozendael, Michel; van der Werf, Guido R.; Wiedinmyer, Christine; Kaiser, Johannes W.; Sindelarova, Katerina; Guenther, Alex

    2016-08-01

    are suggested in Indochina and during the 2007 fires in southern Europe. Moreover, changes in fire seasonal patterns are suggested; e.g., the seasonal amplitude is reduced over southeast Asia. In Africa, the inversion indicates increased fluxes due to agricultural fires and decreased maxima when natural fires are dominant. The top-down fire emissions are much better correlated with MODIS fire counts than the a priori inventory in regions with small and agricultural fires, indicating that the OMI-based inversion is well-suited to assess the associated emissions. Regarding biogenic sources, significant reductions in isoprene fluxes are inferred in tropical ecosystems (30-40 %), suggesting overestimated basal emission rates in those areas in the bottom-up inventory, whereas strongly positive isoprene emission updates are derived over semiarid and desert areas, especially in southern Africa and Australia. This finding suggests that the parameterization of the soil moisture stress used in MEGAN greatly exaggerates the flux reduction due to drought in those regions. The isoprene emission trends over 2005-2013 are often enhanced after optimization, with positive top-down trends in Siberia (4.2 % year-1) and eastern Europe (3.9 % year-1), likely reflecting forest expansion and warming temperatures, and negative trends in Amazonia (-2.1 % year-1), south China (-1 % year-1), the United States (-3.7 % year-1), and western Europe (-3.3 % year-1), which are generally corroborated by independent studies, yet their interpretation warrants further investigation.

  10. Estimating Source Recurrence Rates for Probabilistic Tsunami Hazard Analysis (PTHA)

    NASA Astrophysics Data System (ADS)

    Geist, E. L.; Parsons, T.

    2004-12-01

    A critical factor in probabilistic tsunami hazard analysis (PTHA) is estimating the average recurrence rate for tsunamigenic sources. Computational PTHA involves aggregating runup values derived from numerical simulations for many far-field and local sources, primarily earthquakes, each with a specified probability of occurrence. Computational PTHA is the primary method used in the ongoing FEMA pilot study at Seaside, Oregon. For a Poissonian arrival time model, the probability for a given source is dependent on a single parameter: the mean inter-event time of the source. In other probability models, parameters such as aperiodicity are also included. In this study, we focus on methods to determine the recurrence rates for large, shallow subduction zone earthquakes. For earthquakes below about M=8, recurrence rates can be obtained from modified Gutenberg-Richter distributions that are constrained by the tectonic moment rate for individual subduction zones. However, significant runup from far-field sources is commonly associated with the largest magnitude earthquakes, for which the recurrence rates are poorly constrained by the tail of empirical frequency-magnitude relationships. For these earthquakes, paleoseismic evidence of great earthquakes can be used to establish recurrence rates. Because the number of geologic horizons representing great earthquakes along a particular subduction zone is limited, special techniques are needed to account for open intervals before the first and after the last observed events. Uncertainty in age dates for the horizons also has to be included in estimating recurrence rates and aperiodicity. A Monte Carlo simulation is performed in which a random sample of earthquake times is drawn from a specified probability distribution with varying average recurrence rates and aperiodicities. A recurrence rate can be determined from the mean rate of all random samples that fit the observations, or a range of rates can be carried through the

  11. Evaluation of backward Lagrangian stochastic (bLS) model to estimate gas emissions from complex sources based on numerical simulations

    NASA Astrophysics Data System (ADS)

    Wang, Wei; Liu, Wenqing; Zhang, Tianshu; Ren, Manyan

    2013-03-01

    The focus of the paper is application of an inverse-dispersion technique based on a backward Lagrangian stochastic (bLS) model in order to calculate gas-emission rates from industrial complexes. While the bLS technique is attractive for these types of sources, the bLS calculation must assume a spatial configuration for the source. Therefore, results are presented herein of numerical simulations designed to study the sensitivity of emissions calculations to the assumption of source configuration for complex industrial sources. We discuss how measurement fetch, concentration sensor height, and optical path length influence the accuracy of emission estimation. Through simulations, we identify an improved sensor configuration in order to reduce emission-calculation errors caused by an incorrect source-configuration assumption. It is concluded that, with respect to our defined source, the optimal measurement fetch may be between 200 m and 300 m; also, the ideal measurement height is probably between 2.0 m and 2.5 m. With choices within these two ranges, a path length of about 200 m is adequate, and greater path lengths, above 200 m, result in no substantial improvement in emission calculations.

  12. Quantifying Spatial and Temporal Variability of Methane Emissions from a Complex Area Source: Case Study of a Central Indiana Landfill

    NASA Astrophysics Data System (ADS)

    Cambaliza, M. O. L.; Bogner, J. E.; Green, R. B.; Shepson, P. B.; Thoma, E. D.; Foster-wittig, T. A.; Spokas, K.

    2014-12-01

    Atmospheric methane is a powerful greenhouse gas that is responsible for about 17% of the total direct radiative forcing from long-lived greenhouse gases (IPCC 2013). While the global emission of methane is relatively well quantified, the temporal and spatial variability of methane emissions from individual area or point sources are still poorly understood. Using 4 field methods (aircraft-based mass balance, tracer correlation, vertical radial plume mapping, and static chambers) and a new field-validated process-based model (California Landfill Methane Inventory Model, CALMIM 5.4), we investigated both the total emissions from a central Indiana landfill as well as the partitioned emissions inclusive of methanotrophic oxidation for the various cover soils. This landfill is an upwind source for the city of Indianapolis, so the resolution of m2 to km2 scale emissions, as well as understanding the temporal variability for this complex area source, contributes to improved regional inventory calculations. Emissions for the site as a whole were measured using both an aircraft-based mass balance approach as well as a ground-based tracer correlation method, permitting direct comparison of the strengths, limitations, and uncertainties of these two approaches. Because US landfills are highly-engineered and composed of daily, intermediate, and final cover areas with differing thicknesses, composition, and implementation of gas recovery, we also expected different emission signatures and strengths from the various cover areas. Thus we also deployed static chambers and vertical radial plume mapping to quantify the spatial variability of emissions from the thinner daily and intermediate cover areas. Understanding the daily, seasonal and annual emission rates from a landfill is not trivial, and usually requires a combination of measurement and modeling approaches. Thus, our unique data set provides an opportunity to gain an improved understanding of the emissions from a complex

  13. Contribution of Changing Sources and Sinks to the Growth Rate of Atmospheric Methane Concentrations for the Last Two Decades

    NASA Technical Reports Server (NTRS)

    Matthews, Elaine; Walter, B.; Bogner, J.; Sarma, D.; Portney, B.; Hansen, James (Technical Monitor)

    2000-01-01

    In situ measurements of atmospheric methane concentrations begun in the early 1980s show decadal trends, as well as large interannual variations, in growth rate. Recent research indicates that while wetlands can explain several of the large growth anomalies for individual years, the decadal trend may be the combined effect of increasing sinks, due to increases in tropospheric OH, and stabilizing sources. We discuss new 20-year histories of annual, global source strengths for all major methane sources, i.e., natural wetlands, rice cultivation, ruminant animals, landfills, fossil fuels, and biomass burning, and present estimates of the temporal pattern of the sink required to reconcile these sources and atmospheric concentrations over the time period. Analysis of the individual emission sources, together with model-derived estimates of the OH sink strength, indicates that the growth rate of atmospheric methane observed over the last 20 years can only be explained by a combination of changes in source emissions and an increasing tropospheric sink.

  14. VOLATILE ORGANIC COMPOUND EMISSION RATES FROM MIXED DECIDUOUS AND CONIFEROUS FORESTS IN NORTHERN WISCONSIN, USA

    EPA Science Inventory

    Biogenic emissions of volatile organic compounds (VOC) from forests play an important role in regulating the atmospheric trace gas composition including global tropospheric ozone concentrations. However, more information is needed on VOC emission rates from different forest regio...

  15. VOLATILE ORGANIC COMPOUND EMISSION RATES FROM MIXED DECIDUOUS AND CONIFEROUS FORESTS IN NORTHERN WISCONSIN, USA

    EPA Science Inventory

    Biogenic emissions of volatile organic compounds (VOC) from forests play an important role in regulating the atmospheric trace gas composition including global tropospheric ozone concentrations. However, more information is needed on VOC emission rates from different forest regio...

  16. Global mercury emissions to the atmosphere from anthropogenic and natural sources

    NASA Astrophysics Data System (ADS)

    Pirrone, N.; Cinnirella, S.; Feng, X.; Finkelman, R. B.; Friedli, H. R.; Leaner, J.; Mason, R.; Mukherjee, A. B.; Stracher, G. B.; Streets, D. G.; Telmer, K.

    2010-07-01

    This paper provides an up-to-date assessment of global mercury emissions from anthropogenic and natural sources. On an annual basis, natural sources account for 5207 Mg of mercury released to the global atmosphere, including the contribution from re-emission processes, which are emissions of previously deposited mercury originating from anthropogenic and natural sources, and primary emissions from natural reservoirs. Anthropogenic sources, which include a large number of industrial point sources, are estimated to account for 2320 Mg of mercury emitted annually. The major contributions are from fossil-fuel fired power plants (810 Mg yr-1), artisanal small scale gold mining (400 Mg yr-1), non-ferrous metals manufacturing (310 Mg yr-1), cement production (236 Mg yr-1), waste disposal (187 Mg yr-1) and caustic soda production (163 Mg yr-1). Therefore, our current estimate of global mercury emissions suggests that the overall contribution from natural sources (primary emissions + re-emissions) and anthropogenic sources is nearly 7527 Mg per year, the uncertainty associated with these estimates are related to the typology of emission sources and source regions.

  17. Global mercury emissions to the atmosphere from anthropogenic and natural sources

    NASA Astrophysics Data System (ADS)

    Pirrone, N.; Cinnirella, S.; Feng, X.; Finkelman, R. B.; Friedli, H. R.; Leaner, J.; Mason, R.; Mukherjee, A. B.; Stracher, G. B.; Streets, D. G.; Telmer, K.

    2010-02-01

    This paper provides an up-to-date assessment of global mercury emissions from anthropogenic and natural sources. On an annual basis, natural sources account for 5207 Mg of mercury released to the global atmosphere, including the contribution from re-emission processes, which are emissions of previously deposited mercury originating from anthropogenic and natural sources, and primary emissions from natural reservoirs. Anthropogenic sources, which include a large number of industrial point sources, are estimated to account for 2320 Mg of mercury emitted annually. The major contributions are from fossil-fuel fired power plants (810 Mg yr-1), artisanal small scale gold mining (400 Mg yr-1), non-ferrous metals manufacturing (310 Mg yr-1), cement production (236 Mg yr-1), waste disposal (187 Mg yr-1) and caustic soda production (163 Mg yr-1). Therefore, our current estimate of global mercury emissions suggests that the overall contribution from natural sources (primary emissions+re-emissions) and anthropogenic sources is nearly 7527 Mg per year, the uncertainty associated with these estimates are related to the typology of emission sources and source regions.

  18. CO J = 3-2 Emission from the ``Water Fountain'' Sources IRAS 16342-3814 and IRAS 18286-0959

    NASA Astrophysics Data System (ADS)

    Imai, Hiroshi; He, Jin-Hua; Nakashima, Jun-Ichi Ukita, Nobuharu; Deguchi, Shuji; Koning, Nico

    2009-12-01

    We observed CO J = 3-2 emission from ``water-fountain'' sources, which exhibit high-velocity collimated stellar jets traced by H2O maser emission, with the Atacama Submillimeter Telescope Experiment (ASTE) 10 m telescope. We detected CO emission from two sources: IRAS 16342-3814 and IRAS 18286-0959. The IRAS 16342-3814 CO emission exhibits a spectrum that could be well fit to a Gaussian profile, rather than to a parabolic profile, with a velocity width (FWHM) of 158±6km s-1 and an intensity peak at VLSR = 50±2 km s-1. The mass-loss rate of the star is estimated to be ˜2.9 × 10-5Modot yr-1. Our morpho-kinematic models suggest that the CO emission is optically thin, and associated with a bipolar outflow rather than with a (cold and relatively small) torus. The IRAS 18286-0959 CO emission has a velocity width (FWHM) of 3.0±0.2 km s-1, smaller than typically seen in AGB envelopes. The narrow velocity width of the CO emission suggests that it originates from either an interstellar molecular cloud or a slowly-rotating circumstellar envelope that harbors the H2O maser source.

  19. Estimates of solid waste disposal rates and reduction targets for landfill gas emissions

    NASA Astrophysics Data System (ADS)

    Powell, Jon T.; Townsend, Timothy G.; Zimmerman, Julie B.

    2016-02-01

    Landfill disposal of municipal solid waste represents one of the largest anthropogenic global methane emission sources, and recent policy approaches have targeted significant reductions of these emissions to combat climate change in the US (ref. ). The efficacy of active gas collection systems in the US was examined by analysing performance data, including fire occurrence, from more than 850 landfills. A generalized linear model showed that the operating status of a landfill--open and actively receiving waste or closed--was the most significant predictor of collection system performance. Gas collection systems at closed landfills were statistically significantly more efficient (p < 0.001) and on average 17 percentage points more efficient than those at open landfills, but open landfills were found to represent 91% of all landfill methane emissions. These results demonstrate the clear need to target open landfills to achieve significant near-term methane emission reductions. This observation is underscored by landfill disposal rates in the US significantly exceeding previously reported national estimates, with this study reporting 262 million tonnes in the year 2012 compared with 122 million tonnes in 2012 as estimated by the US Environmental Protection Agency.

  20. Opacity meter for monitoring exhaust emissions from non-stationary sources

    DOEpatents

    Dec, John Edward

    2000-01-01

    Method and apparatus for determining the opacity of exhaust plumes from moving emissions sources. In operation, a light source is activated at a time prior to the arrival of a diesel locomotive at a measurement point, by means of a track trigger switch or the Automatic Equipment Identification system, such that the opacity measurement is synchronized with the passage of an exhaust plume past the measurement point. A beam of light from the light source passes through the exhaust plume of the locomotive and is detected by a suitable detector, preferably a high-rate photodiode. The light beam is well-collimated and is preferably monochromatic, permitting the use of a narrowband pass filter to discriminate against background light. In order to span a double railroad track and provide a beam which is substantially stronger than background, the light source, preferably a diode laser, must provide a locally intense beam. A high intensity light source is also desirable in order to increase accuracy at the high sampling rates required. Also included is a computer control system useful for data acquisition, manipulation, storage and transmission of opacity data and the identification of the associated diesel engine to a central data collection center.

  1. Methane emissions in the US and Canada: contributions of various source sectors and evolution of emissions over time

    NASA Astrophysics Data System (ADS)

    Miller, S. M.; Michalak, A. M.; Wofsy, S. C.; Andrews, A. E.; Biraud, S.; Dlugokencky, E. J.; Fischer, M. L.; Janssens-Maenhout, G.; Kort, E. A.; Miller, B. R.; Miller, J. B.; Montzka, S. A.; Worthy, D. E. J.

    2014-12-01

    In this presentation, we quantify several aspects of methane emissions in the US and Canada using concentration data collected in the atmosphere. First, how much methane in total is emitted from the US and Canada? Second, how much methane is emitted from each individual source across these countries? Third, and finally, how have each of these sources changed in magnitude over the past ten to twenty years? To answer these questions, we use a geostatistical model-data fusion framework and spatial data on land use and economic activity. Using this approach, we estimate the contribution of different source types to methane emissions in the US and compare the magnitude of those anthropogenic emissions against natural fluxes from major wetlands like those near Hudson Bay, Canada. Furthermore, we examine the time-evolution of methane concentrations over regions dominated by agriculture and natural gas extraction and investigate what this data indicates about changes in emissions over time.

  2. Historic emissions from deforestation and forest degradation in Mato Grosso, Brazil: 1) source data uncertainties

    PubMed Central

    2011-01-01

    Background Historic carbon emissions are an important foundation for proposed efforts to Reduce Emissions from Deforestation and forest Degradation and enhance forest carbon stocks through conservation and sustainable forest management (REDD+). The level of uncertainty in historic carbon emissions estimates is also critical for REDD+, since high uncertainties could limit climate benefits from credited mitigation actions. Here, we analyzed source data uncertainties based on the range of available deforestation, forest degradation, and forest carbon stock estimates for the Brazilian state of Mato Grosso during 1990-2008. Results Deforestation estimates showed good agreement for multi-year periods of increasing and decreasing deforestation during the study period. However, annual deforestation rates differed by > 20% in more than half of the years between 1997-2008, even for products based on similar input data. Tier 2 estimates of average forest carbon stocks varied between 99-192 Mg C ha-1, with greatest differences in northwest Mato Grosso. Carbon stocks in deforested areas increased over the study period, yet this increasing trend in deforested biomass was smaller than the difference among carbon stock datasets for these areas. Conclusions Estimates of source data uncertainties are essential for REDD+. Patterns of spatial and temporal disagreement among available data products provide a roadmap for future efforts to reduce source data uncertainties for estimates of historic forest carbon emissions. Specifically, regions with large discrepancies in available estimates of both deforestation and forest carbon stocks are priority areas for evaluating and improving existing estimates. Full carbon accounting for REDD+ will also require filling data gaps, including forest degradation and secondary forest, with annual data on all forest transitions. PMID:22208947

  3. 40 CFR Table 2 to Subpart Xxxx of... - Emission Limits for Tire Cord Production Affected Sources

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 13 2012-07-01 2012-07-01 false Emission Limits for Tire Cord...: Rubber Tire Manufacturing Pt. 63, Subpt. XXXX, Table 2 Table 2 to Subpart XXXX of Part 63—Emission Limits for Tire Cord Production Affected Sources As stated in § 63.5986, you must comply with the emission...

  4. 40 CFR Table 2 to Subpart Xxxx of... - Emission Limits for Tire Cord Production Affected Sources

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 12 2010-07-01 2010-07-01 true Emission Limits for Tire Cord... POLLUTANTS FOR SOURCE CATEGORIES National Emissions Standards for Hazardous Air Pollutants: Rubber Tire Manufacturing Pt. 63, Subpt. XXXX, Table 2 Table 2 to Subpart XXXX of Part 63—Emission Limits for Tire Cord...

  5. 40 CFR Table 2 to Subpart Xxxx of... - Emission Limits for Tire Cord Production Affected Sources

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 13 2014-07-01 2014-07-01 false Emission Limits for Tire Cord...: Rubber Tire Manufacturing Pt. 63, Subpt. XXXX, Table 2 Table 2 to Subpart XXXX of Part 63—Emission Limits for Tire Cord Production Affected Sources As stated in § 63.5986, you must comply with the emission...

  6. 40 CFR Table 2 to Subpart Xxxx of... - Emission Limits for Tire Cord Production Affected Sources

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 12 2011-07-01 2009-07-01 true Emission Limits for Tire Cord... POLLUTANTS FOR SOURCE CATEGORIES National Emissions Standards for Hazardous Air Pollutants: Rubber Tire Manufacturing Pt. 63, Subpt. XXXX, Table 2 Table 2 to Subpart XXXX of Part 63—Emission Limits for Tire Cord...

  7. 40 CFR Table 2 to Subpart Xxxx of... - Emission Limits for Tire Cord Production Affected Sources

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 13 2013-07-01 2012-07-01 true Emission Limits for Tire Cord...: Rubber Tire Manufacturing Pt. 63, Subpt. XXXX, Table 2 Table 2 to Subpart XXXX of Part 63—Emission Limits for Tire Cord Production Affected Sources As stated in § 63.5986, you must comply with the emission...

  8. 40 CFR Table 1 to Subpart Xxxx of... - Emission Limits for Tire Production Affected Sources

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 13 2013-07-01 2012-07-01 true Emission Limits for Tire Production... SOURCE CATEGORIES (CONTINUED) National Emissions Standards for Hazardous Air Pollutants: Rubber Tire Manufacturing Pt. 63, Subpt. XXXX, Table 1 Table 1 to Subpart XXXX of Part 63—Emission Limits for Tire...

  9. Local to regional emission sources affecting mercury fluxes to New York lakes

    NASA Astrophysics Data System (ADS)

    Bookman, Revital; Driscoll, Charles T.; Engstrom, Daniel R.; Effler, Steven W.

    Lake-sediment records across the Northern Hemisphere show increases in atmospheric deposition of anthropogenic mercury (Hg) over the last 150 years. Most of the previous studies have examined remote lakes affected by the global atmospheric Hg reservoir. In this study, we present Hg flux records from lakes in an urban/suburban setting of central New York affected also by local and regional emissions. Sediment cores were collected from the Otisco and Skaneateles lakes from the Finger Lakes region, Cross Lake, a hypereutrophic lake on the Seneca River, and Glacial Lake, a small seepage lake with a watershed that corresponds with the lake area. Sediment accumulation rates and dates were established by 210Pb. The pre-anthropogenic regional atmospheric Hg flux was estimated to be 3.0 μg m -2 yr -1 from Glacial Lake, which receives exclusively direct atmospheric deposition. Mercury fluxes peaked during 1971-2001, and were 3 to more than 30 times greater than pre-industrial deposition. Land use change and urbanization in the Otisco and Cross watersheds during the last century likely enhanced sediment loads and Hg fluxes to the lakes. Skaneateles and Glacial lakes have low sediment accumulation rates, and thus are excellent indicators for atmospheric Hg deposition. In these lakes, we found strong correlations with emission records for the Great Lakes region that markedly increased in the early 1900s, and peaked during WWII and in the early 1970s. Declines in modern Hg fluxes are generally evident in the core records. However, the decrease in sediment Hg flux at Glacial Lake was interrupted and has increased since the early 1990s probably due to the operation of new local emission sources. Assuming the global Hg reservoir tripled since the pre-industrial period, the contribution of local and regional emission sources to central New York lakes was estimated to about 80% of the total atmospheric Hg deposition.

  10. Modeling and Electrostatic Focusing for a Field Emission Electron Source

    DTIC Science & Technology

    2013-06-01

    mechanisms of the beam formation, transport, field emission energy distributions, the effects of the emission properties, and parametric studies are...metals, the valence electrons possess the conduction energy band and are described by Sommerfeld free electron gas model with Fermi- Dirac statistics...which defines the electrons energy distribution. For the emission from not electrical conductors the Sommerfeld theory of metals with Fermi- Dirac

  11. Soil carbon dioxide emissions from the Mojave desert: Isotopic evidence for a carbonate source

    NASA Astrophysics Data System (ADS)

    Soper, Fiona M.; McCalley, Carmody K.; Sparks, Kimberlee; Sparks, Jed P.

    2017-01-01

    Arid soils represent a substantial carbonate pool and may participate in surface-atmosphere CO2 exchange via a diel cycle of carbonate dissolution and exsolution. We used a Keeling plot approach to determine the substrate δ13C of CO2 emitted from carbonate-dominated soils in the Mojave desert and found evidence for a nonrespiratory source that increased with surface temperature. In dry soils at 25-30°C, the CO2 substrate had δ13C values of -19.4 ± 4.2‰, indicative of respiration of organic material (soil organic matter = -23.1 ± 0.8‰). CO2 flux increased with temperature; maximum fluxes occurred above 60°C, where δ13CO2 substrate (-7.2‰ ± 2.8‰) approached soil carbonate values (0.2 ± 0.2‰). In wet soils, CO2 emissions were not temperature dependent, and δ13CO2 substrate was lower in vegetated soils with higher flux rates, higher organic C content, and potential root respiration. These data provide the first direct evidence of CO2 emissions from alkaline desert soils derived from an abiotic source and that diurnal emission patterns are strongly driven by surface temperature.

  12. Diurnal Variation in the Basal Emission Rate of Isoprene

    Treesearch

    Jennifer Funk; Clive G. Jones; Christine J. Baker; Heather M. Fuller; Christian P. Giardina; Manuel T. Lerdua

    2003-01-01

    Isoprene is emitted from numerous plant species and profoundly influences tropospheric chemistry. Due to the short lifetime of isoprene in the atmosphere, developing an understanding of emission patterns at small time scales is essential for modeling regional atmospheric chemistry processes. Previous studies suggest that diurnal fluctuations in isoprene emission may be...

  13. Evaluation of the N2 emission sources from grazed grassland soils

    NASA Astrophysics Data System (ADS)

    Richards, K.; Selbie, D.; Di, H.; Clough, T.; Lanigan, G.; Cameron, K.; Rex, D.; Watson, C.

    2016-12-01

    Grazed grassland livestock systems are often associated with considerable losses of reactive forms of nitrogen (N) to the environment such as nitrate leaching, ammonia and nitrous oxide (N2O) emissions. Previous research has focused on losses to air and water due to the health, economic and environmental impacts of reactive N. Di-nitrogen (N2) emissions from soils are still poorly characterized, both in terms of the processes involved and their magnitude, due to methodological constraints. There have been relatively few studies on N2 losses in vivo and even fewer have examined the relative contribution of the different N2 emission sources. Cow urine was amended with 98 atom% 15N-labelled urea resulting in a urine N concentration of 10 g N L-1 and a 15N enrichment of 45 atom% excess. Two litres of urine was applied to replicated monolith lysimeters at a rate of 100 g N m-2 and N2 and N2O emissions were measured over 123 days using the static chamber technique. Headspace N2 and N2O samples were analyzed for 15N by isotope ratio mass spectrometry in the UC Davis Stable Isotope Facility. Contributions of true denitrification and co-denitrification to N2 emissions were calculated using the 15N flux method. The study found that N2 emissions accounted for 95% of gaseous N loss, with 55.8 g N m-2 emitted as N2 by the process of co-denitrification, compared to only 1.1 g N m-2 from conventional denitrification. This study highlights the large N2 fluxes and the importance of co-denitrification in contributing to N dynamics in urine amended grassland soil.

  14. Emission characteristics of H- ion source with inverse gas magnetron geometrya)

    NASA Astrophysics Data System (ADS)

    Baturin, V. A.; Litvinov, P. A.; Pustovoitov, S. A.; Karpenko, A. Yu.

    2010-02-01

    The work is dedicated to the experimental investigation of the intense volume-plasma H- ion source. Preliminary experimental researches of two parameters of the upgraded source—emission density of H- ions and gas flow—are represented below. In plasma volume of noncesium H- ion source, the conditions for obtaining of increased density of H- ions in the field of adjoining to the emission aperture were realized. The advancing of electrode system of the emission chamber of a source has allowed receiving the value of an emission density of H- ions equal to 600 mA/cm2.

  15. Gaseous mercury emissions from natural sources in Canadian landscapes

    NASA Astrophysics Data System (ADS)

    Schroeder, W. H.; Beauchamp, S.; Edwards, G.; Poissant, L.; Rasmussen, P.; Tordon, R.; Dias, G.; Kemp, J.; van Heyst, B.; Banic, C. M.

    2005-09-01

    Field measurements of mercury air-surface exchange from natural settings were made in various Canadian landscapes. Soil and water samples were analyzed for mercury concentrations, and air-surface exchange fluxes from these substrates were determined using dynamic chamber, micrometeorological, or modeling methods. Environmental variables, including air and soil/water temperature, solar radiation, humidity, and wind speed, were monitored concurrently with the air-surface exchange to better understand the processes affecting the environmental cycling of mercury. Average mercury fluxes from aquatic landscapes ranged from 0.0 to 5.0 ng m-2 h-1 with total mercury concentration in water ranging from 0.3 to 6.5 ng L-1. A significant correlation (R2 = 0.47) was found between gaseous Hg fluxes and total Hg concentration in water. Mean gaseous Hg fluxes from forest soils varied from -0.4 to 2.2 ng m-2 h-1, while those from agricultural fields ranged from 1.1 to 2.9 ng m-2 h-1. Non-mineralized bedrock, sand, and till sites yielded fluxes ranging from -0.03 to 5.9 ng m-2 h-1. Mean fluxes from mercuriferous geological substrates at various locations were large compared to non-mercuriferous sites, ranging from 9.1 to 1760 ng m-2 h-1, and represent natural emissions. The corresponding total mercury substrate concentrations ranged from 0.360 to 180 ppm. A significant correlation (R2 = 0.66) was found between Hg fluxes and total Hg concentrations in mineralized and non-mineralized substrates. These gaseous Hg flux measurements represent a significant contribution to understanding natural mercury cycling, but there are still insufficient data and knowledge of processes to properly scale up fluxes from natural sources in Canada.

  16. GLOBAL METHANE EMISSIONS FROM MINOR ANTHROPOGENIC SOURCES AND BIOFUEL COMBUSTION IN RESIDENTIAL STOVES (JOURNAL)

    EPA Science Inventory

    Most global methane (CH4) budgets have failed to include emissions from a diverse group of minor anthropogenic sources. Individually, these minor sources emit small quantities of CH4, but collectively, their contributions to the budget may be significant. In this paper, CH4 emiss...

  17. RERANKING OF AREA SOURCES IN LIGHT OF SEASONAL/ REGIONAL EMISSION FACTORS AND STATE/LOCAL NEEDS

    EPA Science Inventory

    The report gives results of an effort to provide a better understanding of air pollution area sources and their emissions, to prioritize their importance as emitters of volatile organic compounds (VOCs), and to identify sources for which better emission estimation methodologies a...

  18. 78 FR 25242 - Delegation of New Source Performance Standards and National Emission Standards for Hazardous Air...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-04-30

    ... AGENCY 40 CFR Parts 60 and 61 Delegation of New Source Performance Standards and National Emission... Source Performance Standards (NSPS) and National Emission Standards for Hazardous Air Pollutants (NESHAP... identity or contact information unless you provide it in the body of your comment. If you send email...

  19. GLOBAL METHANE EMISSIONS FROM MINOR ANTHROPOGENIC SOURCES AND BIOFUEL COMBUSTION IN RESIDENTIAL STOVES (JOURNAL)

    EPA Science Inventory

    Most global methane (CH4) budgets have failed to include emissions from a diverse group of minor anthropogenic sources. Individually, these minor sources emit small quantities of CH4, but collectively, their contributions to the budget may be significant. In this paper, CH4 emiss...

  20. RERANKING OF AREA SOURCES IN LIGHT OF SEASONAL/ REGIONAL EMISSION FACTORS AND STATE/LOCAL NEEDS

    EPA Science Inventory

    The report gives results of an effort to provide a better understanding of air pollution area sources and their emissions, to prioritize their importance as emitters of volatile organic compounds (VOCs), and to identify sources for which better emission estimation methodologies a...

  1. 76 FR 35744 - Amendments to National Emission Standards for Hazardous Air Pollutants for Area Sources: Plating...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-06-20

    ...On June 12, 2008, EPA issued national emission standards for control of hazardous air pollutants (HAP) for the plating and polishing area source category under section 112 of the Clean Air Act (CAA). In today's action, EPA is taking direct final action to amend the national emission standards for HAP (NESHAP) for the plating and polishing area source category. These final amendments clarify......

  2. A smart repetitive-rate wideband high power microwave source

    SciTech Connect

    Li, Wei; Zhang, Jun; Qian, Bao-liang; Yang, Han-wu; Zhang, Zi-cheng

    2016-01-15

    A smart repetitive-rate wideband High Power Microwave (HPM) source based on the A6 Magnetron with Diffraction Output is described in this paper. The length of the HPM source is 30 cm and its weight is 35 kg. Computer simulations show that the source can produce microwave with central frequency of 1.91 GHz and bandwidth of about 11%. Experimental measurements show that the output microwave power from the source reaches in maximum 110 MW when the input electric power from the pulsed driver is ∼500 MW, which gives the power conversion efficiency 22%. Central frequency of the output HPM in the experiment is 1.94 GHz with the bandwidth ranging from 1.82 GHz to 2.02 GHz. The jitter of the output HPM power is lower than 3 dB when the source operates in the repetition mode with 50 Hz rate.

  3. 40 CFR 63.843 - Emission limits for existing sources.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ..., operate, and maintain equipment to capture and control POM emissions from each paste production plant. (1) The emission capture system shall be installed and operated to meet the generally accepted engineering... alternative control device to the applicable regulatory authority for review and approval. The request...

  4. 40 CFR 63.843 - Emission limits for existing sources.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ..., operate, and maintain equipment to capture and control POM emissions from each paste production plant. (1) The emission capture system shall be installed and operated to meet the generally accepted engineering... alternative control device to the applicable regulatory authority for review and approval. The request...

  5. 40 CFR 63.843 - Emission limits for existing sources.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ..., operate, and maintain equipment to capture and control POM emissions from each paste production plant. (1) The emission capture system shall be installed and operated to meet the generally accepted engineering... alternative control device to the applicable regulatory authority for review and approval. The request...

  6. [Status and needs research for on-line monitoring of VOCs emissions from stationary sources].

    PubMed

    Wang, Qiang; Zhou, Gang; Zhong, Qi; Zhao, Jin-Bao; Yang, Kai

    2013-12-01

    Based on atmospheric volatile organic compounds (VOCs) pollution control requirements during the twelfth-five year plan and the current status of monitoring and management in the world, instrumental architecture and technical characteristics of continuous emission monitoring systems (CEMS) for VOCs emission from stationary sources are investigated and researched. Technological development needs of VOCs emission on-line monitoring techniques for stationary sources in China are proposed from the system sampling pretreatment technology and analytical measurement techniques.

  7. Particulate metals and organic compounds from electronic and tobacco-containing cigarettes: comparison of emission rates and secondhand exposure.

    PubMed

    Saffari, Arian; Daher, Nancy; Ruprecht, Ario; De Marco, Cinzia; Pozzi, Paolo; Boffi, Roberto; Hamad, Samera H; Shafer, Martin M; Schauer, James J; Westerdahl, Dane; Sioutas, Constantinos

    2014-01-01

    In recent years, electronic cigarettes have gained increasing popularity as alternatives to normal (tobacco-containing) cigarettes. In the present study, particles generated by e-cigarettes and normal cigarettes have been analyzed and the degree of exposure to different chemical agents and their emission rates were quantified. Despite the 10-fold decrease in the total exposure to particulate elements in e-cigarettes compared to normal cigarettes, specific metals (e.g. Ni and Ag) still displayed a higher emission rate from e-cigarettes. Further analysis indicated that the contribution of e-liquid to the emission of these metals is rather minimal, implying that they likely originate from other components of the e-cigarette device or other indoor sources. Organic species had lower emission rates during e-cigarette consumption compared to normal cigarettes. Of particular note was the non-detectable emission of polycyclic aromatic hydrocarbons (PAHs) from e-cigarettes, while substantial emission of these species was observed from normal cigarettes. Overall, with the exception of Ni, Zn, and Ag, the consumption of e-cigarettes resulted in a remarkable decrease in secondhand exposure to all metals and organic compounds. Implementing quality control protocols on the manufacture of e-cigarettes would further minimize the emission of metals from these devices and improve their safety and associated health effects.

  8. 40 CFR 49.138 - Rule for the registration of air pollution sources and the reporting of emissions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... pollution source, ambient air, British thermal unit (Btu), emission, emission factor, emission unit... pollution sources and the reporting of emissions. 49.138 Section 49.138 Protection of Environment... Reservations in Epa Region 10 § 49.138 Rule for the registration of air pollution sources and the reporting...

  9. 40 CFR 49.138 - Rule for the registration of air pollution sources and the reporting of emissions.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... pollution source, ambient air, British thermal unit (Btu), emission, emission factor, emission unit... pollution sources and the reporting of emissions. 49.138 Section 49.138 Protection of Environment... Reservations in Epa Region 10 § 49.138 Rule for the registration of air pollution sources and the reporting...

  10. 40 CFR 49.138 - Rule for the registration of air pollution sources and the reporting of emissions.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... pollution source, ambient air, British thermal unit (Btu), emission, emission factor, emission unit... pollution sources and the reporting of emissions. 49.138 Section 49.138 Protection of Environment... Reservations in Epa Region 10 § 49.138 Rule for the registration of air pollution sources and the reporting...

  11. 40 CFR 49.138 - Rule for the registration of air pollution sources and the reporting of emissions.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... pollution source, ambient air, British thermal unit (Btu), emission, emission factor, emission unit... pollution sources and the reporting of emissions. 49.138 Section 49.138 Protection of Environment... Reservations in Epa Region 10 § 49.138 Rule for the registration of air pollution sources and the reporting...

  12. Emission Spectroscopy measurement of hybrid ECR-Helicon plasma source parameters

    NASA Astrophysics Data System (ADS)

    Hala, Ahmed

    2015-09-01

    Optical emission spectroscopy measurement of plasma temperature and density were conducted on KACST hybrid plasma source. The hybrid source involves ECR and helicon source operated simultanously. The results indicate that the ECR alone density is higher than the density of the combined sources while the combined temperature is lower.

  13. A 2009 Mobile Source Carbon Dioxide Emissions Inventory for the University of Central Florida.

    PubMed

    Clifford, Johanna M; Cooper, C David

    2012-09-01

    A mobile source carbon dioxide (CO2) emissions inventory for the University of Central Florida (UCF) has been completed. Fora large urban university, more than 50% of the CO2 emissions can come from mobile sources, and the vast majority of mobile source emissions come from on-road sources: personal vehicles and campus shuttles carrying students, faculty, staff and administrators to and from the university as well as on university business trips. In addition to emissions from on-road vehicles, emissions from airplane-based business travel are significant, along with emissions from nonroad equipment such as lawnmowers, leaf blowers, and small maintenance vehicles utilized on campus. UCF has recently become one of the largest universities in the nation (with over 58,000 students enrolled in the fall 2011 semester) and emits a substantial amount of CO2 in the Central Florida area. For this inventory, students, faculty, staff and administrators were first surveyed to determine their commuting distances and frequencies. Information was also gathered on vehicle type and age distribution of the personal vehicles of students, faculty, administrators, and staff as well as their bus, car-pool, and alternate transportation usage. The latest US. Environmental Protection Agency (EPA)-approved mobile source emissions model, Motor Vehicle Emissions Simulator (MOVES2010a), was used to calculate the emissions from on-road vehicles, and UCF fleet gasoline consumption records were used to calculate the emissions from nonroad equipment and from on-campus UCF fleet vehicles. The results of this UCF mobile source emissions inventory were compared with those for another large U.S. university. With the growing awareness of global climate change, a number of colleges/universities and other organizations are completing greenhouse gas emission inventories. Assumptions often are made in order to calculate mobile source emissions, but without field data or valid reasoning, the accuracy of those

  14. Applications of Ground-based Mobile Atmospheric Monitoring: Real-time Characterization of Source Emissions and Ambient Concentrations

    NASA Astrophysics Data System (ADS)

    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

  15. Film dosimetry calibration method for pulsed-dose-rate brachytherapy with an 192Ir source.

    PubMed

    Schwob, Nathan; Orion, Itzhak

    2007-05-01

    192Ir sources have been widely used in clinical brachytherapy. An important challenge is to perform dosimetric measurements close to the source despite the steep dose gradient. The common, inexpensive silver halide film is a classic two-dimensional integrator dosimeter and would be an attractive solution for these dose measurements. The main disadvantage of film dosimetry is the film response to the low-energy photon. Since the photon energy spectrum is known to vary with depth, the sensitometric curves are expected to be dependent on depth. The purpose of this study is to suggest a correction method for silver halide film dosimetry that overcomes the response changes at different depths. Sensitometric curves have been obtained at different depths with verification film near a 1 Ci 192Ir pulsed-dose-rate source. The depth dependence of the film response was observed and a correction function was established. The suitability of the method was tested through measurement of the radial dose profile and radial dose function. The results were compared to Monte Carlo-simulated values according to the TG43 formalism. Monte Carlo simulations were performed separately for the beta and gamma source emissions, using the EGS4 code system, including the low-energy photon and electron transport optimization procedures. The beta source emission simulation showed that the beta dose contribution could be neglected and therefore the film-depth dependence could not be attributed to this part of the source radioactivity. The gamma source emission simulations included photon-spectra collection at several depths. The results showed a depth-dependent softening of the photon spectrum that can explain the film-energy dependence.

  16. 40 CFR 75.83 - Calculation of Hg mass emissions and heat input rate.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... heat input rate. 75.83 Section 75.83 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Calculation of Hg mass emissions and heat input rate. The owner or operator shall calculate Hg mass emissions and heat input rate in accordance with the procedures in sections 9.1 through 9.3 of appendix F to...

  17. Crowd-Sourcing Management Activity Data to Drive GHG Emission Inventories in the Land Use Sector

    NASA Astrophysics Data System (ADS)

    Paustian, K.; Herrick, J.

    2015-12-01

    Greenhouse gas (GHG) emissions from the land use sector constitute the largest source category for many countries in Africa. Enhancing C sequestration and reducing GHG emissions on managed lands in Africa has to potential to attract C financing to support adoption of more sustainable land management practices that, in addition to GHG mitigation, can provide co-benefits of more productive and climate-resilient agroecosystems. However, robust systems to measure and monitor C sequestration/GHG reductions are currently a significant barrier to attracting more C financing to land use-related mitigation efforts.Anthropogenic GHG emissions are driven by a variety of environmental factors, including climate and soil attributes, as well as human-activities in the form of land use and management practices. GHG emission inventories typically use empirical or process-based models of emission rates that are driven by environmental and management variables. While a lack of field-based flux and C stock measurements are a limiting factor for GHG estimation, we argue that an even greater limitation may be availabiity of data on the management activities that influence flux rates, particularly in developing countries in Africa. In most developed countries there is a well-developed infrastructure of agricultural statistics and practice surveys that can be used to drive model-based GHG emission estimations. However, this infrastructure is largely lacking in developing countries in Africa. While some activity data (e.g. land cover change) can be derived from remote sensing, many key data (e.g., N fertilizer practices, residue management, manuring) require input from the farmers themselves. The explosive growth in cellular technology, even in many of the poorest parts of Africa, suggests the potential for a new crowd-sourcing approach and direct engagement with farmers to 'leap-frog' the land resource information model of developed countries. Among the many benefits of this approach

  18. Greenhouse gas emissions from tropical forest degradation: an underestimated source.

    PubMed

    Pearson, Timothy R H; Brown, Sandra; Murray, Lara; Sidman, Gabriel

    2017-12-01

    The degradation of forests in developing countries, particularly those within tropical and subtropical latitudes, is perceived to be an important contributor to global greenhouse gas emissions. However, the impacts of forest degradation are understudied and poorly understood, largely because international emission reduction programs have focused on deforestation, which is easier to detect and thus more readily monitored. To better understand and seize opportunities for addressing climate change it will be essential to improve knowledge of greenhouse gas emissions from forest degradation. Here we provide a consistent estimation of forest degradation emissions between 2005 and 2010 across 74 developing countries covering 2.2 billion hectares of forests. We estimated annual emissions of 2.1 billion tons of carbon dioxide, of which 53% were derived from timber harvest, 30% from woodfuel harvest and 17% from forest fire. These percentages differed by region: timber harvest was as high as 69% in South and Central America and just 31% in Africa; woodfuel harvest was 35% in Asia, and just 10% in South and Central America; and fire ranged from 33% in Africa to only 5% in Asia. Of the total emissions from deforestation and forest degradation, forest degradation accounted for 25%. In 28 of the 74 countries, emissions from forest degradation exceeded those from deforestation. The results of this study clearly demonstrate the importance of accounting greenhouse gases from forest degradation by human activities. The scale of emissions presented indicates that the exclusion of forest degradation from national and international GHG accounting is distorting. This work helps identify where emissions are likely significant, but policy developments are needed to guide when and how accounting should be undertaken. Furthermore, ongoing research is needed to create and enhance cost-effective accounting approaches.

  19. What Is the Source of Quiet Sun Transition Region Emission?

    NASA Astrophysics Data System (ADS)

    Schmit, D. J.; De Pontieu, Bart

    2016-11-01

    Dating back to the first observations of the on-disk corona, there has been a qualitative link between the photosphere’s magnetic network and enhanced transition-temperature plasma emission. These observations led to the development of a general model that describes emission structures through the partitioning of the atmospheric volume with different magnetic loop geometries that exhibit different energetic equilibria. Does the internetwork produce transition-temperature emission? What fraction of network flux connects to the corona? How does quiet Sun emission compare with low-activity Sun-like stars? In this work, we revisit the canonical model of the quiet Sun, with high-resolution observations from the Interface Region Imaging Spectrograph (IRIS) and HMI in hand, to address those questions. We use over 900 deep exposures of Si iv 1393 Å from IRIS along with nearly simultaneous HMI magnetograms to quantify the correlation between transition-temperature emission structures and magnetic field concentrations through a number of novel statistics. Our observational results are coupled with analysis of the Bifrost MHD model and a large-scale potential field model. Our results paint a complex portrait of the quiet Sun. We measure an emission signature in the distant internetwork that cannot be attributed to network contribution. We find that the dimmest regions of emission are not linked to the local vertical magnetic field. Using the MHD simulation, we categorize the emission contribution from cool mid-altitude loops and high-altitude coronal loops and discuss the potential emission contribution of spicules. Our results provide new constraints on the coupled solar atmosphere so that we can build on our understanding of how dynamic thermal and magnetic structures generate the observed phenomena in the transition region.

  20. Nonlinear Source -" Receptor Relationship due to Interactions between Atmospheric Constituents, Water Cycle and Biogenic Emissions

    NASA Astrophysics Data System (ADS)

    Kinne, S.; Feichter, J.; Rast, S.; Bey, I.; Folberth, G.; Pozzoli, L.; Kloster, S.; Stier, P.

    2007-05-01

    Specific economic sectors or source regions emit a wide variety of air pollutants which influence climate and air quality. This includes emissions of greenhouse gases, chemical species which affect the oxidation capacity of the atmosphere and the concentrations of ozone and methane, and aerosol particles or aerosol precursors. Regional climate respectively weather controls transport and removal of pollutants, chemical transformation pathways, particle formation rate and sink processes as well as emissions from natural sources. Interactions between aerosols and trace gases modify their global and regional distributions. Thus, climatic and environmental impacts are not only controlled by amount and chemical composition of pollutant emissions but in addition also by their interactions and the local meteorological conditions in the source region. For the development of mitigation strategies to minimize adverse conditions attributed to climate change and air pollution we need a better understanding of the role of source location, impact of interactions and feedbacks and of the influence of climate change on the chemical composition of the atmosphere. To demonstrate interactions and feedbacks between the cycles of gaseous and particulate atmospheric constituents, the water cycle, the biosphere and the changing climate we will present results of a series of numerical model simulations. Investigations include interactions between greenhouse gas warming, water cycle and aerosol cycle (Feichter et al., 2004), between aerosol cycles (Stier et al., 2006), between marine biogeochemistry and aerosol cycles (Kloster et al., 2006), and between gas-phase air chemistry and aerosol constituents (Pozzoli et al., 2007). The presentation discusses possible interactions and feedbacks and emphasizes the need for a better integration of the different Earth system components in climate and air quality models. Finally, the question whether anthropogenic emissions from different regions

  1. Comparison of emissions from on-road sources using a mobile laboratory under various driving and operational sampling modes

    NASA Astrophysics Data System (ADS)

    Zavala, M.; Herndon, S. C.; Wood, E. C.; Jayne, J. T.; Nelson, D. D.; Trimborn, A. M.; Dunlea, E.; Knighton, W. B.; Mendoza, A.; Allen, D. T.; Kolb, C. E.; Molina, M. J.; Molina, L. T.

    2009-01-01

    Mobile sources produce a significant fraction of the total anthropogenic emissions burden in large cities and have harmful effects on air quality at multiple spatial scales. Mobile emissions are intrinsically difficult to estimate due to the large number of parameters affecting the emissions variability within and across vehicles types. The MCMA-2003 Campaign in Mexico City has showed the utility of using a mobile laboratory to sample and characterize specific classes of motor vehicles to better quantify their emissions characteristics as a function of their driving cycles. The technique clearly identifies "high emitter" vehicles via individual exhaust plumes, and also provides fleet average emission rates. We have applied this technique to Mexicali during the Border Ozone Reduction and Air Quality Improvement Program (BORAQIP) for the Mexicali-Imperial Valley in 2005. We analyze the variability of measured emission ratios for emitted NOx, CO, specific VOCs, NH3, and some primary fine particle components and properties by deploying a mobile laboratory in roadside stationary sampling, chase and fleet average operational sampling modes. The measurements reflect various driving modes characteristic of the urban fleets. The observed variability for all measured gases and particle emission ratios is greater for the chase and roadside stationary sampling than for fleet average measurements. The fleet average sampling mode captured the effects of traffic conditions on the measured on-road emission ratios, allowing the use of fuel-based emission ratios to assess the validity of traditional "bottom-up" emissions inventories. Using the measured on-road emission ratios, we estimate CO and NOx mobile emissions of 175±62 and 10.4±1.3 metric tons/day, respectively, for the gasoline vehicle fleet in Mexicali. Comparisons with similar on-road emissions data from Mexico City indicated that fleet average NO emission ratios were around 20% higher in Mexicali than in Mexico City

  2. Comparison of emission ratios from on-road sources using a mobile laboratory under various driving and operational sampling modes

    NASA Astrophysics Data System (ADS)

    Zavala, M.; Herndon, S. C.; Wood, E. C.

    2008-04-01

    Mobile sources produce a significant fraction of the total anthropogenic emissions burden in large cities and have harmful effects on air quality at multiple spatial scales. Mobile emissions are intrinsically difficult to estimate due to the large number of parameters affecting the emissions variability within and across vehicles types. The MCMA-2003 Campaign in Mexico City has showed the utility of using a mobile laboratory to sample and characterize specific classes of motor vehicles to better quantify their emissions characteristics as a function of their driving cycles. The technique clearly identifies "high emitter" vehicles via individual exhaust plumes, and also provides fleet average emission rates. We have applied this technique to Mexicali during the Border Ozone Reduction and Air Quality Improvement Program for the Mexicali-Imperial Valley in 2005. In this paper we analyze the variability of measured emission ratios for emitted NOx, CO, specific VOCs, NH3, and some primary fine particle components and properties obtained during the Border Ozone Reduction and Air Quality Improvement Program for the Mexicali-Imperial Valley in 2005 by deploying a mobile laboratory in roadside stationary sampling, chase and fleet average operational sampling modes. The measurements reflect various driving modes characteristic of the urban fleets. The observed variability for all measured gases and particle emission ratios is greater for the chase and roadside stationary sampling than for fleet average measurements. The fleet average sampling mode captured the effects of traffic conditions on the measured on-road emission ratios, allowing the use of fuel-based emission ratios to assess the validity of traditional "bottom-up" emissions inventories. Using the measured on-road emission ratios, we estimate CO and NOx mobile emissions of 175±62 and 10.4±1.3 metric tons/day, respectively, for the gasoline vehicle fleet in Mexicali. Comparisons with similar on-road emissions data

  3. Using an Explicit Emission Tagging Method in Global Modeling of Source-Receptor Relationships for Black Carbon in the Arctic: Variations, Sources and Transport Pathways

    SciTech Connect

    Wang, Hailong; Rasch, Philip J.; Easter, Richard C.; Singh, Balwinder; Zhang, Rudong; Ma, Po-Lun; Qian, Yun; Ghan, Steven J.; Beagley, Nathaniel

    2014-11-27

    We introduce an explicit emission tagging technique in the Community Atmosphere Model to quantify source-region-resolved characteristics of black carbon (BC), focusing on the Arctic. Explicit tagging of BC source regions without perturbing the emissions makes it straightforward to establish source-receptor relationships and transport pathways, providing a physically consistent and computationally efficient approach to produce a detailed characterization of the destiny of regional BC emissions and the potential for mitigation actions. Our analysis shows that the contributions of major source regions to the global BC burden are not proportional to the respective emissions due to strong region-dependent removal rates and lifetimes, while the contributions to BC direct radiative forcing show a near-linear dependence on their respective contributions to the burden. Distant sources contribute to BC in remote regions mostly in the mid- and upper troposphere, having much less impact on lower-level concentrations (and deposition) than on burden. Arctic BC concentrations, deposition and source contributions all have strong seasonal variations. Eastern Asia contributes the most to the wintertime Arctic burden. Northern Europe emissions are more important to both surface concentration and deposition in winter than in summer. The largest contribution to Arctic BC in the summer is from Northern Asia. Although local emissions contribute less than 10% to the annual mean BC burden and deposition within the Arctic, the per-emission efficiency is much higher than for major non-Arctic sources. The interannual variability (1996-2005) due to meteorology is small in annual mean BC burden and radiative forcing but is significant in yearly seasonal means over the Arctic. When a slow aging treatment of BC is introduced, the increase of BC lifetime and burden is source-dependent. Global BC forcing-per-burden efficiency also increases primarily due to changes in BC vertical distributions. The

  4. Validation of flux measurements with artificial sources: simulating CH4 from cows and NH3 emissions from medium plot scales

    NASA Astrophysics Data System (ADS)

    Sintermann, Jörg; Felber, Raphael; Häni, Christoph; Ammann, Christof; Neftel, Albrecht

    2014-05-01

    Mitigation of ammonia (NH3) emissions with detrimental environmental effects as well as of greenhouse gas emissions (GHG: CO2, N2O, CH4) are key challenges faced by the agricultural production sector. While NH3 originates mainly from polluted surfaces, e.g. after slurry application, the main source for CH4 emissions are cows and other ruminating animals, representing point sources. There are two widespread state-of-the-art techniques to determine agricultural emissions: eddy covariance (EC) flux measurements and Lagrangian stochastic (LS) dispersion modelling, namely the WindTrax (WT) model. Whereas GHG emissions can be measured with both techniques, NH3 emissions are usually not feasible with EC measurements due to the stickiness of NH3 molecules on surfaces. In addition, point sources render difficulties for the interpretation of EC flux data. We tested the EC technique and the WT model using artificial sources with known gas release rates. i) The effect of a point source on EC fluxes was investigated by placing an artificial CH4 source with known release rate upwind of the EC tower at two different heights and during different wind conditions. ii) The WT model was checked with a NH3 release grid of 314 m2 of known source strength. Ambient NH3 concentrations were measured by open path DOAS systems and impinger sampling. The CH4 concentration timeseries influenced by the point source showed a similar pattern as in the presence of cows upwind of the EC system. CH4 release rates from the point source were reproduced by the EC flux measurement with stationary background conditions only. The experiments with the NH3 release showed that WT performs well for emission determination, even in complex terrain (asphalt surrounded by grassland) with associated micrometeorology, given a realistic description of the vertical profile of wind velocity. Calculated gas recoveries ranged between 73 to 105%. Such a result is encouraging considering the immanent uncertainties from a

  5. Component Failure Rate Data Sources for Probabilistic Safety and Reliability

    SciTech Connect

    L. C. Cadwallader; S. A. Eide

    2010-09-01

    Probabilistic safety methods are being used in several industries, including chemical, manufacturing, and energy. When performing reliability studies or using probabilistic safety approaches, a basic need arises for input data on failure rates of the mechanical, electrical, instrumentation and control, and other components that comprise the engineering systems in the facility. Some companies have many types of data stored and can retrieve these in-house data for such uses. Other companies hire consultants to perform safety assessments; the consulting firms often use their own data bases. For those analysts who do not have either of those options available, this paper presents some data sources that are retrievable from the literature. These data sources have been evaluated with a basic rating of usefulness for analysis work, and each has a description of what data can be found in the citation that can be used to support assessments in industry. The accessibility of data documents via the internet is also described.

  6. Black carbon emissions from Russian diesel sources: case study of Murmansk

    NASA Astrophysics Data System (ADS)

    Evans, M.; Kholod, N.; Malyshev, V.; Tretyakova, S.; Gusev, E.; Yu, S.; Barinov, A.

    2015-02-01

    Black carbon (BC) is a potent pollutant because of its effects on climate change, ecosystems and human health. Black carbon has a particularly pronounced impact as a climate forcer in the Arctic because of its effect on snow albedo and cloud formation. We have estimated BC emissions from diesel sources in Murmansk Region and Murmansk City, the largest city in the world above the Arctic Circle. In this study we developed a detailed inventory of diesel sources including on-road vehicles, off-road transport (mining, locomotives, construction and agriculture), fishing and diesel generators. For on-road transport, we conducted several surveys to understand the vehicle fleet and driving patterns, and, for all sources, we also relied on publicly available local data sets and analysis. We calculated that BC emission in Murmansk Region were 0.40 Gg in 2012. The mining industry is the largest source of BC emissions in the region, emitting 70% of all BC emissions because of its large diesel consumption and absence of emissions controls. On-road vehicles are the second largest source emitting about 12% of emissions. Old heavy duty trucks are the major source of emissions. Emission controls on new vehicles limit total emissions from on-road transportation. Vehicle traffic and fleet surveys show that many of the older cars on the registry are lightly or never used. We also estimated that total BC emissions from diesel sources in Russia were 56.7 Gg in 2010, and on-road transport contributed 55% of diesel BC emissions. Agricultural machinery is also a significant source Russia-wide, in part because of the lack of controls on off-road vehicles.

  7. Black carbon emissions from Russian diesel sources: case study of Murmansk

    NASA Astrophysics Data System (ADS)

    Evans, M.; Kholod, N.; Malyshev, V.; Tretyakova, S.; Gusev, E.; Yu, S.; Barinov, A.

    2015-07-01

    Black carbon (BC) is a potent pollutant because of its effects on climate change, ecosystems and human health. Black carbon has a particularly pronounced impact as a climate forcer in the Arctic because of its effect on snow albedo and cloud formation. We have estimated BC emissions from diesel sources in the Murmansk Region and Murmansk City, the largest city in the world above the Arctic Circle. In this study we developed a detailed inventory of diesel sources including on-road vehicles, off-road transport (mining, locomotives, construction and agriculture), ships and diesel generators. For on-road transport, we conducted several surveys to understand the vehicle fleet and driving patterns, and, for all sources, we also relied on publicly available local data sets and analysis. We calculated that BC emissions in the Murmansk Region were 0.40 Gg in 2012. The mining industry is the largest source of BC emissions in the region, emitting 69 % of all BC emissions because of its large diesel consumption and absence of emissions controls. On-road vehicles are the second largest source, emitting about 13 % of emissions. Old heavy duty trucks are the major source of emissions. Emission controls on new vehicles limit total emissions from on-road transportation. Vehicle traffic and fleet surveys show that many of the older cars on the registry are lightly or never used. We also estimated that total BC emissions from diesel sources in Russia were 50.8 Gg in 2010, and on-road transport contributed 49 % of diesel BC emissions. Agricultural machinery is also a significant source Russia-wide, in part because of the lack of controls on off-road vehicles.

  8. Black carbon emissions from Russian diesel sources. Case study of Murmansk

    SciTech Connect

    Evans, M.; Kholod, N.; Malyshev, V.; Tretyakova, S.; Gusev, E.; Yu, S.; Barinov, A.

    2015-07-27

    Black carbon (BC) is a potent pollutant because of its effects on climate change, ecosystems and human health. Black carbon has a particularly pronounced impact as a climate forcer in the Arctic because of its effect on snow albedo and cloud formation. We have estimated BC emissions from diesel sources in the Murmansk Region and Murmansk City, the largest city in the world above the Arctic Circle. In this study we developed a detailed inventory of diesel sources including on-road vehicles, off-road transport (mining, locomotives, construction and agriculture), ships and diesel generators. For on-road transport, we conducted several surveys to understand the vehicle fleet and driving patterns, and, for all sources, we also relied on publicly available local data sets and analysis. We calculated that BC emissions in the Murmansk Region were 0.40 Gg in 2012. The mining industry is the largest source of BC emissions in the region, emitting 69 % of all BC emissions because of its large diesel consumption and absence of emissions controls. On-road vehicles are the second largest source, emitting about 13 % of emissions. Old heavy duty trucks are the major source of emissions. Emission controls on new vehicles limit total emissions from on-road transportation. Vehicle traffic and fleet surveys show that many of the older cars on the registry are lightly or never used. We also estimated that total BC emissions from diesel sources in Russia were 50.8 Gg in 2010, and on-road transport contributed 49 % of diesel BC emissions. Agricultural machinery is also a significant source Russia-wide, in part because of the lack of controls on off-road vehicles.

  9. Black carbon emissions from Russian diesel sources. Case study of Murmansk

    DOE PAGES

    Evans, M.; Kholod, N.; Malyshev, V.; ...

    2015-07-27

    Black carbon (BC) is a potent pollutant because of its effects on climate change, ecosystems and human health. Black carbon has a particularly pronounced impact as a climate forcer in the Arctic because of its effect on snow albedo and cloud formation. We have estimated BC emissions from diesel sources in the Murmansk Region and Murmansk City, the largest city in the world above the Arctic Circle. In this study we developed a detailed inventory of diesel sources including on-road vehicles, off-road transport (mining, locomotives, construction and agriculture), ships and diesel generators. For on-road transport, we conducted several surveys tomore » understand the vehicle fleet and driving patterns, and, for all sources, we also relied on publicly available local data sets and analysis. We calculated that BC emissions in the Murmansk Region were 0.40 Gg in 2012. The mining industry is the largest source of BC emissions in the region, emitting 69 % of all BC emissions because of its large diesel consumption and absence of emissions controls. On-road vehicles are the second largest source, emitting about 13 % of emissions. Old heavy duty trucks are the major source of emissions. Emission controls on new vehicles limit total emissions from on-road transportation. Vehicle traffic and fleet surveys show that many of the older cars on the registry are lightly or never used. We also estimated that total BC emissions from diesel sources in Russia were 50.8 Gg in 2010, and on-road transport contributed 49 % of diesel BC emissions. Agricultural machinery is also a significant source Russia-wide, in part because of the lack of controls on off-road vehicles.« less

  10. Simultaneous and multi-point measurement of ammonia emanating from human skin surface for the estimation of whole body dermal emission rate.

    PubMed

    Furukawa, Shota; Sekine, Yoshika; Kimura, Keita; Umezawa, Kazuo; Asai, Satomi; Miyachi, Hayato

    2017-05-15

    Ammonia is one of the members of odor gases and a possible source of odor in indoor environment. However, little has been known on the actual emission rate of ammonia from the human skin surface. Then, this study aimed to estimate the whole-body dermal emission rate of ammonia by simultaneous and multi-point measurement of emission fluxes of ammonia employing a passive flux sampler - ion chromatography system. Firstly, the emission fluxes of ammonia were non-invasively measured for ten volunteers at 13 sampling positions set in 13 anatomical regions classified by Kurazumi et al. The measured emission fluxes were then converted to partial emission rates using the surface body areas estimated by weights and heights of volunteers and partial rates of 13 body regions. Subsequent summation of the partial emission rates provided the whole body dermal emission rate of ammonia. The results ranged from 2.9 to 12mgh(-1) with an average of 5.9±3.2mgh(-1) per person for the ten healthy young volunteers. The values were much greater than those from human breath, and thus the dermal emission of ammonia was found more significant odor source than the breath exhalation in indoor environment. Copyright © 2017 Elsevier B.V. All rights reserved.

  11. Non-point source mercury emission from the Idrija Hg-mine region: GIS mercury emission model.

    PubMed

    Kocman, David; Horvat, Milena

    2011-08-01

    A mercury emission model was developed to estimate non-point source mercury (Hg) emissions occurring over the year from the Idrijca River catchment, draining the area of the world's second largest Hg mine in Idrija, Slovenia. Site-specific empirical correlations between the measured Hg emission fluxes and the parameters controlling the emission (comprising substrate Hg content, soil temperature, solar radiation and soil moisture) were incorporated into the mercury emission model developed using Geographic Information System technology. In this way, the spatial distribution and significance of the most polluted sites that need to be properly managed was assessed. The modelling results revealed that annually approximately 51 kg of mercury are emitted from contaminated surfaces in the catchment (640 km(2)), highlighting that emission from contaminated surfaces contributes significantly to the elevated Hg concentrations in the ambient air of the region. Very variable meteorological conditions in the modelling domain throughout the year resulted in the high seasonal and spatial variations of mercury emission fluxes observed. Moreover, it was found that mercury emission fluxes from surfaces in the Idrija region are 3-4 fold higher than the values commonly used in models representing emissions from global mercuriferous belts. Sensitivity and model uncertainty analysis indicated the importance of knowing not only the amount but also the type of mercury species and their binding in soils in future model development.

  12. Historic Emissions from Deforestation and Forest Degradation in Mato Grosso, Brazil: 1. Source Data Uncertainties

    NASA Technical Reports Server (NTRS)

    Morton, Douglas C.; Sales, Marcio H.; Souza, Carlos M., Jr.; Griscom, Bronson

    2011-01-01

    Historic carbon emissions are an important foundation for proposed efforts to Reduce Emissions from Deforestation and forest Degradation and enhance forest carbon stocks through conservation and sustainable forest management (REDD+). The level of uncertainty in historic carbon emissions estimates is also critical for REDD+, since high uncertainties could limit climate benefits from mitigation actions. Here, we analyzed source data uncertainties based on the range of available deforestation, forest degradation, and forest carbon stock estimates for the Brazilian state of Mato Grosso during 1990-2008. Results: Deforestation estimates showed good agreement for multi-year trends of increasing and decreasing deforestation during the study period. However, annual deforestation rates differed by >20% in more than half of the years between 1997-2008, even for products based on similar input data. Tier 2 estimates of average forest carbon stocks varied between 99-192 Mg C/ha, with greatest differences in northwest Mato Grosso. Carbon stocks in deforested areas increased over the study period, yet this increasing trend in deforested biomass was smaller than the difference among carbon stock datasets for these areas. Conclusions: Patterns of spatial and temporal disagreement among available data products provide a roadmap for future efforts to reduce source data uncertainties for estimates of historic forest carbon emissions. Specifically, regions with large discrepancies in available estimates of both deforestation and forest carbon stocks are priority areas for evaluating and improving existing estimates. Full carbon accounting for REDD+ will also require filling data gaps, including forest degradation and secondary forest, with annual data on all forest transitions.

  13. GLOBAL INVENTORY OF VOLATILE COMPOUND EMISSIONS FROM ANTHROPOGENIC SOURCES

    EPA Science Inventory

    The report describes a global inventory anthropogenic volatile organic compound (VOC) emissions that includes a separate inventory for each of seven pollutant groups--paraffins, olefins, aromatics, formaldehyde, other aldehydes, other aromatics, and marginally reactive compounds....

  14. GLOBAL INVENTORY OF VOLATILE COMPOUND EMISSIONS FROM ANTHROPOGENIC SOURCES

    EPA Science Inventory

    The report describes a global inventory anthropogenic volatile organic compound (VOC) emissions that includes a separate inventory for each of seven pollutant groups--paraffins, olefins, aromatics, formaldehyde, other aldehydes, other aromatics, and marginally reactive compounds....

  15. RATE OF ACCLIMATION OF THE CAPACITY FOR ISOPRENE EMISSION IN RESPONSE TO LIGHT AND TEMPERATURE

    EPA Science Inventory

    Isoprene emission from plants accounts for nearly half of all non-methane hydrocarbons entering the atmosphere. Light and temperature regulate the instantaneous rate of isoprene emission, but there is increasing evidence that they also affect the capacity for isoprene emission (i...

  16. RATE OF ACCLIMATION OF THE CAPACITY FOR ISOPRENE EMISSION IN RESPONSE TO LIGHT AND TEMPERATURE

    EPA Science Inventory

    Isoprene emission from plants accounts for nearly half of all non-methane hydrocarbons entering the atmosphere. Light and temperature regulate the instantaneous rate of isoprene emission, but there is increasing evidence that they also affect the capacity for isoprene emission (i...

  17. Source emission and model evaluation of formaldehyde from composite and solid wood furniture in a full-scale chamber

    NASA Astrophysics Data System (ADS)

    Liu, Xiaoyu; Mason, Mark A.; Guo, Zhishi; Krebs, Kenneth A.; Roache, Nancy F.

    2015-12-01

    This paper describes the measurement and model evaluation of formaldehyde source emissions from composite and solid wood furniture in a full-scale chamber at different ventilation rates for up to 4000 h using ASTM D 6670-01 (2007). Tests were performed on four types of furniture constructed of different materials and from different manufacturers. The data were used to evaluate two empirical emission models, i.e., a first-order and power-law decay model. The experimental results showed that some furniture tested in this study, made only of solid wood and with less surface area, had low formaldehyde source emissions. The effect of ventilation rate on formaldehyde emissions was also examined. Model simulation results indicated that the power-law decay model showed better agreement than the first-order decay model for the data collected from the tests, especially for long-term emissions. This research was limited to a laboratory study with only four types of furniture products tested. It was not intended to comprehensively test or compare the large number of furniture products available in the market place. Therefore, care should be taken when applying the test results to real-world scenarios. Also, it was beyond the scope of this study to link the emissions to human exposure and potential health risks.

  18. Megacity and country emissions from combustion sources-Buenos Aires-Argentina

    NASA Astrophysics Data System (ADS)

    Dawidowski, L.; Gomez, D.; Matranga, M.; D'Angiola, A.; Oreggioni, G.

    2010-12-01

    Historic time series (1970-2006) emissions of greenhouse gases and air pollutants arising from stationary and mobile combustion sources were estimated at national level for Argentina and at regional level for the metropolitan area of Buenos Aires (MABA). All emissions were estimated using a bottom-up approach following the IPCC good practice guidance. For mobile sources, national emissions include all transport categories. Regional emissions account thus far only for on-road. For national emissions, methodologies and guidance by the IPCC were employed, applying the highest possible tier and using: i)country-specific emission factors for carbon and sulphur and technology-based information for other species, ii)activity data from energy balance series (1970-2007), and iii)complementary information concerning the non-energy use of fuels. Regional emissions in 2006 were estimated in-depth using a technology-based approach for the city of Buenos Aires (CBA) and the 24 neighboring districts composing the MABA. A regional emissions factors database was developed to better characterize Latin American fleets and driving conditions employing COPERT III-IV algorithms and emission factors measured in dynamometers and circulating vehicles in Argentina, Brazil, Chile and Colombia. Past emissions were back estimated from 2005 to 1970 using the best available information, which differs greatly among categories, spatial disaggregation and time periods. The time series of stationary and mobile combustion sources at the national and regional level allowed the identification of distinct patterns. National greenhouse gas emissions in 2006 amounted to ~ 150 million ton CO2-equivalent, 70% of which were contributed by stationary sources. On-road transport was the major contributor within mobile sources (28.1 %). The increasing emissions trends are dominated by on-road transport, agriculture and residential categories while the variability is largely associated with energy industries

  19. Identifying sensitive sources and key control handles for the reduction of greenhouse gas emissions from wastewater treatment.

    PubMed

    Sweetapple, Christine; Fu, Guangtao; Butler, David

    2014-10-01

    This research investigates the effects of adjusting control handle values on greenhouse gas emissions from wastewater treatment, and reveals critical control handles and sensitive emission sources for control through the combined use of local and global sensitivity analysis methods. The direction of change in emissions, effluent quality and operational cost resulting from variation of control handles individually is determined using one-factor-at-a-time sensitivity analysis, and corresponding trade-offs are identified. The contribution of each control handle to variance in model outputs, taking into account the effects of interactions, is then explored using a variance-based sensitivity analysis method, i.e., Sobol's method, and significant second order interactions are discovered. This knowledge will assist future control strategy development and aid an efficient design and optimisation process, as it provides a better understanding of the effects of control handles on key performance indicators and identifies those for which dynamic control has the greatest potential benefits. Sources with the greatest variance in emissions, and therefore the greatest need to monitor, are also identified. It is found that variance in total emissions is predominantly due to changes in direct N2O emissions and selection of suitable values for wastage flow rate and aeration intensity in the final activated sludge reactor is of key importance. To improve effluent quality, costs and/or emissions, it is necessary to consider the effects of adjusting multiple control handles simultaneously and determine the optimum trade-off.

  20. Influence of phosphine flow rate on Si growth rate in gas source molecular beam epitaxy

    NASA Astrophysics Data System (ADS)

    Gao, F.; Huang, D. D.; Li, J. P.; Lin, Y. X.; Kong, M. Y.; Sun, D. Z.; Li, J. M.; Lin, L. Y.

    2000-12-01

    As reported by other authors, we have also observed that the Si growth rate decreases with increasing phosphine (PH 3) flow rate in gas source Si molecular beam epitaxy using phosphorous (P) as a n-type dopant. Why small quantity PH 3 can affect Si growth rate? Up to now, the quantitative characterization of PH 3 flow influence on Si growth rate is little known. In this letter, the PH 3 influence will be analyzed in detail and a model considering strong P surface segregation and its absorption of hydrogen will be proposed to characterize the effect.

  1. Sources of persistent organic pollutants emission on the territory of Belarus

    NASA Astrophysics Data System (ADS)

    Kakareka, Sergey V.

    The paper considers selected persistent organic pollutants (POPs) atmospheric emission evaluation on the territory of Belarus for main source categories. The procedure applied was based on the UNECE EMEP methodology. Data of industrial statistics, production processes analysis and relevant emission factors were used. For a number of sources, only quality and semi-quality emission evaluation was conducted, due to the lack of information for the selection of emission factors or statistical data relevant. In the paper, emissions of the following groups of pollutants are discussed: dioxins/furans (PCDD/PCDF) and polychlorinated biphenyls (PCB) as requested for EMEP database (Protocol on Persistent Organic Pollutants to the convention of 1979 on Long-range Transboundary Air Pollution in Europe and Annexes I, II, or III to the Protocol, 1998). PAH emission and selected chlorinated pesticides input also requested by EMEP will be described in other issues. Estimations have showed that Belarus as a whole is not a large emission source of such POPs as dioxins. Its share in European emissions is significantly below 1%. This can be explained by the fact that in Belarus there are no such large dioxin emission sources like sintering, waste incineration, non-ferrous industry. But some important sources of dioxins/furans for instance, open burning are not included in quantitative estimation now. The main contribution to dioxin emissions is by firewood and peat combustion. Only electric steel smelting plant can be considered as a large emission point source. Leakage from transformers and damaged capacitors was estimated as the main source of polychlorinated biphenyls (PCB) discharged into the environment: dielectric fluids with PCB are still in use in electrical equipment.

  2. Volatile organic compound concentrations and emission rates measured over one year in a new manufactured house

    SciTech Connect

    Hodgson, Alfred T.; Nabinger, Steven J.; Persily, Andrew K.

    2004-09-01

    A study to measure indoor concentrations and emission rates of volatile organic compounds (VOCs), including formaldehyde, was conducted in a new, unoccupied manufactured house installed at the National Institute of Standards and Technology (NIST) campus. The house was instrumented to continuously monitor indoor temperature and relative humidity, heating and air conditioning system operation, and outdoor weather. It also was equipped with an automated tracer gas injection and detection system to estimate air change rates every 2 h. Another automated system measured indoor concentrations of total VOCs with a flame ionization detector every 30 min. Active samples for the analysis of VOCs and aldehydes were collected indoors and outdoors on 12 occasions from August 2002 through September 2003. Individual VOCs were quantified by thermal desorption to a gas chromatograph with a mass spectrometer detector (GC/MS). Formaldehyde and acetaldehyde were quantified by high performance liquid chromatography (HPLC). Weather conditions changed substantially across the twelve active sampling periods. Outdoor temperatures ranged from 7 C to 36 C. House air change rates ranged from 0.26 h{sup -1} to 0.60 h{sup -1}. Indoor temperature was relatively constant at 20 C to 24 C for all but one sampling event. Indoor relative humidity (RH) ranged from 21% to 70%. The predominant and persistent indoor VOCs included aldehydes (e.g., formaldehyde, acetaldehyde, pentanal, hexanal and nonanal) and terpene hydrocarbons (e.g., a-pinene, 3-carene and d-limonene), which are characteristic of wood product emissions. Other compounds of interest included phenol, naphthalene, and other aromatic hydrocarbons. VOC concentrations were generally typical of results reported for other new houses. Measurements of total VOCs were used to evaluate short-term changes in indoor VOC concentrations. Most of the VOCs probably derived from indoor sources. However, the wall cavity was an apparent source of

  3. Is CO radio line emission a reliable mass-loss-rate estimator for AGB stars?

    NASA Astrophysics Data System (ADS)

    Ramstedt, Sofia; Scḧier, Frederik; Olofsson, Hans

    The final evolutionary stage of low- to intermediate-mass stars, as they evolve along the asymptotic giant branch (AGB), is characterized by mass loss so intense (10-8-10-4 Msol yr-1) that eventually the AGB life time is determined by it. The material lost by the star is enriched in nucleo-synthesized material and thus AGB stars play an important role in the chemical evolution of galaxies. A reliable mass-loss-rate estimator is of utmost importance in order to increase our understanding of late stellar evolution and to reach conclusions about the amount of enriched material recycled by AGB stars. For low-mass-loss-rate AGB stars, modelling of observed rotational CO radio line emission has proven to be a good tool for estimating mass-loss rates [Olofsson et al. (2002) for M-type stars and Schöier & Olofsson (2001) for carbon stars], but several lines are needed to get good constraints. For high-mass-loss-rate objects the situation is more complicated, the main reason being saturation of the optically thick CO lines. Moreover, Kemper et al. (2003) introduced temporal changes in the mass-loss rate, or alternatively, spatially varying turbulent motions, in order to explain observed line-intensity ratios. This puts into question whether it is possible to model the circumstellar envelope using a constant mass-loss rate, or whether the physical structure of the outflow is more complex than normally assumed. We present observations of CO radio line emission for a sample of intermediate- to high-mass-loss-rate AGB stars. The lowest rotational transition line (J =1-0) was observed at OSO and the higher-frequency lines (J =2-1, 3-2, 4-3 and in some cases 6-5) were observed at the JCMT. Using a detailed, non-LTE, radiative transfer model we are able to reproduce observed line ratios (Figure 1) and constrain the mass-loss rates for the whole sample, using a constant mass-loss rate and a "standard" circumstellar envelope model. However, for some objects only a lower limit to

  4. High resolution European emission grids for anthropogenic sources for the years 2003-2007

    NASA Astrophysics Data System (ADS)

    Denier van der Gon, Hugo; Visschedijk, Antoon; Kuenen, Jeroen; van der Brugh, Hans; Dröge, Rianne; Schaap, Martijn

    2010-05-01

    To develop atmospheric services such as forecasting atmospheric composition a combination of meteorological models, atmospheric chemical transport models, satellite observational data and emission grids are needed. The latter are input for the predictive models and need to be as accurate as possible both in time and space. To support the new EU FP7 MACC (Monitoring Atmospheric Composition and Climate) we developed high resolution (1/8 degree x 1/16 degree lon-lat or ~ 7 x7 km) emission grids for UNECE-Europe for the years 2003-2007. These years are the focus of a reanalysis exercise within MACC. Reanalysis datasets are produced with data assimilation and modelling systems applied to the best available observational datasets. Such reanalysed fields of climate and atmospheric composition can be used in other studies (e.g. IPCC) to make more accurate assessments. For the MACC reanalysis years we use a combination of official reported emission data as available from EMEP, the IIASA GAINS model and expert estimates resulting in a consistent emission data set by country by source category for these years. From 2003-2007 emissions of air pollutants decreased by about 5%, although the reduction of NH3 emission was less (2.3%) and SO2 reduction was more (13%). However, more remarkable than the overall changes are the regional differences as well as source sector differences. For example, NOx emissions changed by -12% in the EU15+NOR+CHE, -8% in the EU12 and + 6 % in the non-EU countries. The emissions are distributed using our newly developed year 2005 emission database which is partly developed in EU FP7 MEGAPOLI. This database distinguishes itself from previous emission databases by a much improved spatial allocation of emissions. To this end we checked and updated our point source database by adding new point sources and removing obsolete entries for power plants, refineries and industrial installations. For diffuse sources like transport, residential combustion and

  5. PM 2.5 source profiles for black and organic carbon emission inventories

    NASA Astrophysics Data System (ADS)

    Chow, Judith C.; Watson, John G.; Lowenthal, Douglas H.; Antony Chen, L.-W.; Motallebi, Nehzat

    2011-10-01

    Emission inventories for black or elemental (BC or EC) and organic (OC) carbon can be derived by multiplying PM 2.5 emission estimates by mass fractions of these species in representative source profiles. This study examines the variability of source profiles and its effect on EC emission estimates. An examination of available profiles shows that EC and OC ranged from 6-13% and 35-40% for agricultural burning, 4-33% and 22-68% for residential wood combustion, 6-38% and 24-75% for on-road gasoline vehicles, and 33-74% and 20-47% for on-road heavy-duty diesel vehicles, respectively. Source profiles from the U.S. EPA SPECIATE data base were applied to PM 2.5 emissions from the U.S. EPA National Emissions Inventory for 2005. The total estimated EC emissions of 432 Gg yr -1 was apportioned as 42.5% from biomass burning, 35.4% from non-road mobile sources, 15% from on-road mobile sources, 5.4% from fossil fuel (e.g., coal, oil, and natural gas) combustion in stationary sources, 1% from other stationary industrial sources, and 0.5% from fugitive dust. Considering the variability in available source profiles, BC emission estimates for major sources such as open fires and non-road diesels ranged from 42 to 133 (a factor of 3) and 25 to 100 (a factor of 4) Gg yr -1, respectively. The choice of source profiles can be a major source of uncertainty in national and global BC/EC emission inventories.

  6. GHG emissions during the high-rate production of compost using standard and advanced aeration strategies.

    PubMed

    Puyuelo, B; Gea, T; Sánchez, A

    2014-08-01

    In this study, we have evaluated different strategies for the optimization of the aeration during the active thermophilic stage of the composting process of source-selected Organic Fraction of Municipal Solid Waste (or biowaste) using reactors at bench scale (50L). These strategies include: typical cyclic aeration, oxygen feedback controller and a new self-developed controller based on the on-line maximization of the oxygen uptake rate (OUR) during the process. Results highlight differences found in the emission of most representative greenhouse gases (GHG) emitted from composting (methane and nitrous oxide) as well as in gases typically related to composting odor problems (ammonia as typical example). Specifically, the cyclic controller presents emissions that can double that of OUR controller, whereas oxygen feedback controller shows a better performance with respect to the cyclic controller. A new parameter, the respiration index efficiency, is presented to quantitatively evaluate the GHG emissions and, in consequence, the main negative environmental impact of the composting process. Other aspects such as the stability of the compost produced and the consumption of resources are also evaluated for each controller. Copyright © 2014 Elsevier Ltd. All rights reserved.

  7. Natural gas fugitive emissions rates constrained by global atmospheric methane and ethane.

    PubMed

    Schwietzke, Stefan; Griffin, W Michael; Matthews, H Scott; Bruhwiler, Lori M P

    2014-07-15

    The amount of methane emissions released by the natural gas (NG) industry is a critical and uncertain value for various industry and policy decisions, such as for determining the climate implications of using NG over coal. Previous studies have estimated fugitive emissions rates (FER)--the fraction of produced NG (mainly methane and ethane) escaped to the atmosphere--between 1 and 9%. Most of these studies rely on few and outdated measurements, and some may represent only temporal/regional NG industry snapshots. This study estimates NG industry representative FER using global atmospheric methane and ethane measurements over three decades, and literature ranges of (i) tracer gas atmospheric lifetimes, (ii) non-NG source estimates, and (iii) fossil fuel fugitive gas hydrocarbon compositions. The modeling suggests an upper bound global average FER of 5% during 2006-2011, and a most likely FER of 2-4% since 2000, trending downward. These results do not account for highly uncertain natural hydrocarbon seepage, which could lower the FER. Further emissions reductions by the NG industry may be needed to ensure climate benefits over coal during the next few decades.

  8. Premature deaths attributed to source-specific BC emissions in six urban US regions

    NASA Astrophysics Data System (ADS)

    Turner, Matthew D.; Henze, Daven K.; Capps, Shannon L.; Hakami, Amir; Zhao, Shunliu; Resler, Jaroslav; Carmichael, Gregory R.; Stanier, Charles O.; Baek, Jaemeen; Sandu, Adrian; Russell, Armistead G.; Nenes, Athanasios; Pinder, Rob W.; Napelenok, Sergey L.; Bash, Jesse O.; Percell, Peter B.; Chai, Tianfeng

    2015-11-01

    Recent studies have shown that exposure to particulate black carbon (BC) has significant adverse health effects and may be more detrimental to human health than exposure to PM2.5 as a whole. Mobile source BC emission controls, mostly on diesel-burning vehicles, have successfully decreased mobile source BC emissions to less than half of what they were 30 years ago. Quantification of the benefits of previous emissions controls conveys the value of these regulatory actions and provides a method by which future control alternatives could be evaluated. In this study we use the adjoint of the Community Multiscale Air Quality (CMAQ) model to estimate highly-resolved spatial distributions of benefits related to emission reductions for six urban regions within the continental US. Emissions from outside each of the six chosen regions account for between 7% and 27% of the premature deaths attributed to exposure to BC within the region. While we estimate that nonroad mobile and onroad diesel emissions account for the largest number of premature deaths attributable to exposure to BC, onroad gasoline is shown to have more than double the benefit per unit emission relative to that of nonroad mobile and onroad diesel. Within the region encompassing New York City and Philadelphia, reductions in emissions from large industrial combustion sources that are not classified as EGUs (i.e., non-EGU) are estimated to have up to triple the benefits per unit emission relative to reductions to onroad diesel sectors, and provide similar benefits per unit emission to that of onroad gasoline emissions in the region. While onroad mobile emissions have been decreasing in the past 30 years and a majority of vehicle emission controls that regulate PM focus on diesel emissions, our analysis shows the most efficient target for stricter controls is actually onroad gasoline emissions.

  9. Characterization, concentrations and emission rates of polycyclic aromatic hydrocarbons in the exhaust emissions from in-service vehicles in Damascus

    NASA Astrophysics Data System (ADS)

    Alkurdi, Farouk; Karabet, François; Dimashki, Marwan

    2013-02-01

    Motor vehicles are significant sources of polycyclic aromatic hydrocarbon (PAH) emissions to the urban atmosphere. Improved understanding of PAH emission profiles in mobile sources is the key to determining the viable approach for reducing PAH emissions from motor vehicles. Very limited data is available on the levels of PAH emissions in the urban atmospheres in Syria and no data are currently available on the level of PAH emissions from different combustion sources in the country. The aim of this study was to determine the profile and concentration of PAH in exhaust emissions of light and heavy-duty vehicles running on the roads of Damascus city. Three different types of vehicles (passenger cars, minivans and buses) were selected along with different age groups. Vapor- and particulate-phase PAH were collected from the vehicular exhausts of six in-service vehicles (with/without catalytic converters). High-performance liquid chromatography system, equipped with UV-Visible and fluorescence detectors, was used for the identification and quantification of PAH compounds in the cleaned extracts of the collected samples. The mean concentration of total PAH emissions (sum of 15 compounds) from all types of studied vehicles ranged between 69.28 ± 1.06 μg/m3 for passenger cars equipped with catalytic converters and 2169.41 ± 5.17 μg/m3 for old diesel buses without pollution controls. Values of total benzo(a)pyrene equivalent (∑ B[a]Peq) ranged between 1.868 μg/m3and 37.652 μg/m3. The results obtained in this study showed that the use of catalytic converters resulted into cleaner exhaust compositions and emissions with characteristics that are distinct from those obtained in the absence of catalytic converters.

  10. Fast pulsed operation of a small non-radioactive electron source with continuous emission current control

    SciTech Connect

    Cochems, P.; Kirk, A. T.; Bunert, E.; Runge, M.; Goncalves, P.; Zimmermann, S.

    2015-06-15

    Non-radioactive electron sources are of great interest in any application requiring the emission of electrons at atmospheric pressure, as they offer better control over emission parameters than radioactive electron sources and are not subject to legal restrictions. Recently, we published a simple electron source consisting only of a vacuum housing, a filament, and a single control grid. In this paper, we present improved control electronics that utilize this control grid in order to focus and defocus the electron beam, thus pulsing the electron emission at atmospheric pressure. This allows short emission pulses and excellent stability of the emitted electron current due to continuous control, both during pulsed and continuous operations. As an application example, this electron source is coupled to an ion mobility spectrometer. Here, the pulsed electron source allows experiments on gas phase ion chemistry (e.g., ion generation and recombination kinetics) and can even remove the need for a traditional ion shutter.

  11. Effects of nitrogen application rate, nitrogen synergist and biochar on nitrous oxide emissions from vegetable field in south China

    PubMed Central

    Zhang, Mu; Pang, Yuwan; Huang, Xu; Huang, Qiaoyi

    2017-01-01

    Globally, vegetable fields are the primary source of greenhouse gas emissions. A closed-chamber method together with gas chromatography was used to measure the fluxes of nitrous oxide (N2O) emissions in typical vegetable fields planted with four vegetables sequentially over time in the same field: endive, lettuce, cabbage and sweet corn. Results showed that N2O fluxes occurred in pulses with the N2O emission peak varying greatly among the crops. In addition, N2O emissions were linearly associated with the nitrogen (N) application rate (r = 0.8878, n = 16). Excessive fertilizer N application resulted in N loss through nitrous oxide gas emitted from the vegetable fields. Compared with a conventional fertilization (N2) treatment, the cumulative N2O emissions decreased significantly in the growing seasons of four plant species from an nitrogen synergist (a nitrification inhibitor, dicyandiamide and biochar treatments by 34.6% and 40.8%, respectively. However, the effects of biochar on reducing N2O emissions became more obvious than that of dicyandiamide over time. The yield-scaled N2O emissions in consecutive growing seasons for four species increased with an increase in the N fertilizer application rate, and with continuous application of N fertilizer. This was especially true for the high N fertilizer treatment that resulted in a risk of yield-scaled N2O emissions. Generally, the additions of dicyandiamide and biochar significantly decreased yield-scaled N2O-N emissions by an average of 45.9% and 45.7%, respectively, compared with N2 treatment from the consecutive four vegetable seasons. The results demonstrated that the addition of dicyandiamide or biochar in combination with application of a rational amount of N could provide the best strategy for the reduction of greenhouse gas emissions in vegetable field in south China. PMID:28419127

  12. Effects of nitrogen application rate, nitrogen synergist and biochar on nitrous oxide emissions from vegetable field in south China.

    PubMed

    Yi, Qiong; Tang, Shuanghu; Fan, Xiaolin; Zhang, Mu; Pang, Yuwan; Huang, Xu; Huang, Qiaoyi

    2017-01-01

    Globally, vegetable fields are the primary source of greenhouse gas emissions. A closed-chamber method together with gas chromatography was used to measure the fluxes of nitrous oxide (N2O) emissions in typical vegetable fields planted with four vegetables sequentially over time in the same field: endive, lettuce, cabbage and sweet corn. Results showed that N2O fluxes occurred in pulses with the N2O emission peak varying greatly among the crops. In addition, N2O emissions were linearly associated with the nitrogen (N) application rate (r = 0.8878, n = 16). Excessive fertilizer N application resulted in N loss through nitrous oxide gas emitted from the vegetable fields. Compared with a conventional fertilization (N2) treatment, the cumulative N2O emissions decreased significantly in the growing seasons of four plant species from an nitrogen synergist (a nitrification inhibitor, dicyandiamide and biochar treatments by 34.6% and 40.8%, respectively. However, the effects of biochar on reducing N2O emissions became more obvious than that of dicyandiamide over time. The yield-scaled N2O emissions in consecutive growing seasons for four species increased with an increase in the N fertilizer application rate, and with continuous application of N fertilizer. This was especially true for the high N fertilizer treatment that resulted in a risk of yield-scaled N2O emissions. Generally, the additions of dicyandiamide and biochar significantly decreased yield-scaled N2O-N emissions by an average of 45.9% and 45.7%, respectively, compared with N2 treatment from the consecutive four vegetable seasons. The results demonstrated that the addition of dicyandiamide or biochar in combination with application of a rational amount of N could provide the best strategy for the reduction of greenhouse gas emissions in vegetable field in south China.

  13. Quantitative analysis of directional spontaneous emission spectra from light sources in photonic crystals

    SciTech Connect

    Nikolaev, Ivan S.; Lodahl, Peter; Vos, Willem L.

    2005-05-15

    We have performed angle-resolved measurements of spontaneous-emission spectra from laser dyes and quantum dots in opal and inverse opal photonic crystals. Pronounced directional dependencies of the emission spectra are observed: angular ranges of strongly reduced emission adjoin with angular ranges of enhanced emission. It appears that emission from embedded light sources is affected both by the periodicity and by the structural imperfections of the crystals: the photons are Bragg diffracted by lattice planes and scattered by unavoidable structural disorder. Using a model comprising diffuse light transport and photonic band structure, we quantitatively explain the directional emission spectra. This work provides detailed understanding of the transport of spontaneously emitted light in real photonic crystals, which is essential in the interpretation of quantum optics in photonic-band-gap crystals and for applications wherein directional emission and total emission power are controlled.

  14. Impacts of different emission sources on air quality during March 2001 in the Pearl River Delta (PRD) region

    NASA Astrophysics Data System (ADS)

    Wang, Xuemei; Carmichael, Gregory; Chen, Deliang; Tang, Youhua; Wang, Tijian

    This study focuses on the role played by emissions from transportation, industry and power generation on the concentrations of O 3, CO, NO, NO y and SO 2 in Guangdong province of China. Observational data of the pollutants and numerical modeling of atmospheric chemistry, transport and removal processes with STEM-2K1 and MM5 are used for March 2001. The objective is to identify the relative importance of the three emission sources on the concentrations of the pollutants. In addition, the relative importance of NO x and VOC emissions from the transportation sector for O 3 production is examined. The observations at a rural and an urban site in the region show distinctive characteristics, indicating the importance of local emissions. A comparison of the observed ratios of CO/NO x and SO 2/NO x at the two sites with those derived from the emission inventories show the usefulness of the emission inventories. A control simulation with all emissions included shows a fairly satisfactory performance of the model in terms of the comparison between the observed and modeled concentrations of CO, SO 2, NO y and O 3 at the rural site, although the observed extremes are less well simulated. Three simulations with different emission scenarios suggest that the transportation source was the main contributor to NO x, CO and O 3 concentrations accounting for 34.2%, 33.1% and 17.8% of their total concentrations, respectively. For SO 2 concentration, the main contributor is the power plant sources with a contribution rate of 32.9%. For SO 2, the doubling of emissions from the industry has a much larger effect on the ambient levels than the doubling from the transportation, whereas the increase in the transportation sector sources has approximately twice the effect of the increased industrial emission on O 3. The doubling of emissions from the transportation and industry sources would increase the O 3 concentration by about 26.7% and 8.5% for the whole region. Finally, the O 3/NO z ratio

  15. Source location of the smooth high-frequency radio emissions from Uranus

    SciTech Connect

    Farrell, W.M.; Calvert, W. )

    1989-05-01

    The source location of the smooth high-frequency (SHF) radio emissions from Uranus has been determined using a technique differing from those applied previously. Specifically, by fitting the signal dropouts which occurred as Voyager traversed the hollow center for the emission pattern to a symmetrical cone centered on the source magnetic field direction at the cyclotron frequency, a southern-hemisphere (nightside) source was found at approximately 56{degree} S, 219{degree} W. The half-angle for the hollow portion of the emission pattern was found to be 13{degree}.

  16. Acoustic emission source modeling in a plate using buried moment tensors

    NASA Astrophysics Data System (ADS)

    Joseph, Roshan; Bhuiyan, Md. Yeasin; Giurgiutiu, Victor

    2017-04-01

    Acoustic emission is a widely used and efficient method for structural damage monitoring. Analytical modeling of wave propagation due to dislocations by considering the source as a self-equilibrating moment tensor is a commonly used approach is seismology. In this paper the acoustic emission source definition using moment tensor approach is studied and tried to implement it in thin plates with micro crack acoustic emission source. Depending upon the characteristic of micro crack formed the moment tensor excitation also changes. A study has done to identify the moment tensor components for mod 1, mode 2 or mode 3 like fracture micro crack formation from the classical definition of moment tensor.

  17. The Role of the Jet Emission in Young Radio Sources

    NASA Astrophysics Data System (ADS)

    Migliori, Giulia

    2014-07-01

    We investigated the contribution of the jet to the observed high energy emission in a sample of young and compact radio quasars. For the first time, we compared the Fermi-LAT and Chandra observations of the sample to γ-ray and X-ray luminosities predicted assuming a jet synchrotron and inverse Compton radiative model. The simulations performed for a reasonable set of model parameters and assumptions provide constraints on the minimum jet power (Ljet,kin/Ldisk >0.01), on the contribution of the jet to the X-ray emission, and on the particles to magnetic field energy density ratios.

  18. Modeling Ozone in the Eastern United States Using a Fuel-Based Mobile Source Emissions Inventory

    NASA Astrophysics Data System (ADS)

    Mcdonald, B. C.; Ahmadov, R.; McKeen, S. A.; Kim, S. W.; Frost, G. J.; Trainer, M.

    2015-12-01

    A fuel-based mobile source emissions inventory of nitrogen oxides (NOx) and carbon monoxide (CO) is developed for the continental US. Emissions are mapped for the year 2013, including emissions from on-road gasoline and diesel vehicles, and off-road engines. We find that mobile source emissions of NOx in the National Emissions Inventory 2011 (NEI11) are 50-60% higher than results from this study; mobile sources contribute around half of total US anthropogenic NOx emissions. We model chemistry and transport of emissions from the NEI11 and our fuel-based inventory during the Southeast Nexus (SENEX) Study period in the summer of 2013, using the Weather Research and Forecasting with Chemistry (WRF-Chem) model. In the Eastern US, there is a consistent over-prediction of tropospheric ozone (O3) levels when simulating emissions from the NEI11, with the largest biases located in the Southeastern US. Using our fuel-based inventory, we test O3 sensitivity to lower NOx emissions. We highlight results in the Southeast, a region with significant interactions between anthropogenic and biogenic emissions of ozone precursors. Model results of NOy, CO, and O3 are compared with aircraft measurements made during SENEX.

  19. Compilation of a source profile database for hydrocarbon and OVOC emissions in China

    NASA Astrophysics Data System (ADS)

    Mo, Ziwei; Shao, Min; Lu, Sihua

    2016-10-01

    Source profiles are essential for quantifying the role of volatile organic compound (VOC) emissions in air pollution. This study compiled a database of VOC source profiles in China, with 75 species drawn from five major categories: transportation, solvent use, biomass burning, fossil fuel burning, and industrial processes. Source profiles were updated for diesel vehicles, biomass burning, and residential coal burning by measuring both hydrocarbons and oxygenated VOCs (OVOCs), while other source profiles were derived from the available literature. The OVOCs contributed 53.8% of total VOCs in the profiles of heavy - duty diesel vehicle exhaust and 12.4%-46.3% in biomass and residential coal burning, which indicated the importance of primary OVOCs emissions from combustion-related sources. Taking the national emission inventory from 2008 as an example, we established an approach for assigning source profiles to develop a speciation-specific VOC and OVOC emission inventory. The results showed that aromatics contributed 30% of the total 26 Tg VOCs, followed by alkanes (24%), alkenes (19%) and OVOCs (12%). Aromatics (7.9 Tg) were much higher than in previous results (1.1 Tg and 3.4 Tg), while OVOCs (3.1 Tg) were comparable with the 3.3 Tg and 4.3 Tg reported in studies using profiles from the US. The current emission inventories were built based on emission factors from non-methane hydrocarbon measurements, and therefore the proportions from OVOC emissions was neglected, leading to up to 30% underestimation of total VOC emissions. As a result, there is a need to deploy appropriate emission factors and source profiles that include OVOC measurements to reduce the uncertainty of estimated emissions and chemical reactivity potential.

  20. ON THE EVOLUTION OF ACCRETION RATES IN COMPACT OUTBURST SOURCES

    SciTech Connect

    Mandal, Samir; Chakrabarti, Sandip K. E-mail: chakraba@bose.res.in

    2010-02-20

    Spectra in outburst sources are found to become soft in viscous timescales before going back to hard as in the pre-outburst phase. By using two component accretion disks we show that major characteristics of the spectral evolution can be reproduced. We find that the outburst is possibly caused by a sudden rise in viscosity which gradually converts the sub-Keplerian flow into a Keplerian flow. The decline of the viscosity reduces the Keplerian accretion rate, and the system goes back to hard states. We discuss the genesis of the characteristic shape of the hardness-intensity diagram and reproduce this for the well-known outburst source GRO J1655-40.

  1. A Global inventory of volatile organic compound emissions from anthropogenic sources

    NASA Astrophysics Data System (ADS)

    Piccot, Stephen D.; Watson, Joel J.; Jones, Julian W.

    1992-06-01

    As part of an effort to assess the potential impacts associated with global climate change, the U.S. Environmental Protection Agency's Office of Research and Development is supporting global atmospheric chemistry research by developing global scale estimates of volatile organic compound (VOC) emissions (excluding methane). Atmospheric chemistry models require, as one input, an emissions inventory of VOCs. Consequently, a global inventory of anthro