WorldWideScience

Sample records for hydrocarbon vapor emissions

  1. 33 CFR 157.132 - Cargo tanks: Hydrocarbon vapor emissions.

    Science.gov (United States)

    2010-07-01

    ...(a)(2) or § 157.10c(b)(2) without sufficient segregated ballast tanks or dedicated clean ballast... 33 Navigation and Navigable Waters 2 2010-07-01 2010-07-01 false Cargo tanks: Hydrocarbon vapor... SECURITY (CONTINUED) POLLUTION RULES FOR THE PROTECTION OF THE MARINE ENVIRONMENT RELATING TO TANK...

  2. 33 CFR 157.166 - Hydrocarbon emissions.

    Science.gov (United States)

    2010-07-01

    ... 33 Navigation and Navigable Waters 2 2010-07-01 2010-07-01 false Hydrocarbon emissions. 157.166... Crude Oil Washing (COW) System on Tank Vessels Cow Operations § 157.166 Hydrocarbon emissions. If the... ballasted in that port the hydrocarbon vapors in each tank are contained by a means under § 157.132....

  3. An apparatus for vapor conversion of hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Tabata, K.; Matsumoto, I.

    1983-03-23

    The installation for vapor conversion of hydrocarbons (Uv) with the formation of a mixture of H2 and C02 is a catalyst chamber (KK) filled with longitudinally disposed thin pipes (with thin walls) or with pipe units made of dolomite, MgO or potassium aluminate. These pipes have a multilayered coating (Pk) on their internal and external surfaces (Pv), which contain catalytically active components. Such pipes or pipe units form a honeycombed structure with through longitudinal channels. The catalyst chamber itself is made of a ceramic material and has a heating winding outside for heating the catalyst. To save fuel and to increase the efficiency (KPD) of the heating device, the catalyst chamber is in turn enclosed by two additional shells filled with heat conducting packings which are easily penetrated by the gases being processed. The hydrocarbon vapors or gaseous fuel from the natural gas or methane and the steam are fed through the above cited heat exchange layers with packings into the facial part of the catalytic chamber, in which the conversion of the hydrocarbons occurs with the production of H2 and C02. From the catalyzer layer the mixture of gases and steam goes through a refrigerator into a trap for the steam excess and when it is necessary, into a C02 absorber and then, pure H2 is discharged from the latter. Such a catalytic installation is convenient to use for producing pure H2 from natural gas, methane, propane or kerosene.

  4. BIODEGRADATION OF HYDROCARBON VAPORS IN THE UNSATURATED ZONE

    Science.gov (United States)

    The time-averaged concentration of hydrocarbon and oxygen vapors were measured in the unsaturated zone above the residually contaminated capillary fringe at the U.S. Coast Guard Air Station in Traverse City, Michigan. Total hydrocarbon and oxygen vapor concentrations were observe...

  5. Biodegradation of Petroleum Hydrocarbon Vapors in the Vadose Zone

    Science.gov (United States)

    The current state of practice to estimate the risk from intrusion of vapors of petroleum hydrocarbons from spills of gasoline is to measure the concentration of the chemical of concern in ground water under the spill, use Henry’s Law to estimate a concentration of the chemical ...

  6. Qualitative Analysis of Liquid Hydrocarbon Mixtures by Absorption Spectra of Their Vapors

    Science.gov (United States)

    Vesnin, V. L.

    2016-11-01

    Absorption spectra of saturated vapors of hydrocarbons and their mixtures were studied near their first overtones. Absorption spectra of hydrocarbons in the liquid and vapor states were compared. The ability to analyze qualitatively the compositions of liquid hydrocarbon mixtures using absorption spectra of their vapors was demonstrated. Indirect evidence suggested that the nonlinear absorption as a function of concentration that was seen in liquid hydrocarbon mixtures was negligible in their vapors.

  7. Development of Buoy Mounted Hydrocarbon Vapor Sensors for Use in Local Area Pollution Surveillance Systems

    Science.gov (United States)

    1975-07-01

    PNP transistor as hydrocarbon vapor sensor . . . . 3. Hot wire sensors for hydrocarbons 4. Suitability of an lonlzatlon sensor for... PNP transistors , (A) a radioactive ionlzatlon sensor, and (5) the Taguchl semiconductor gas sensor, TGS. Later, the Esso piezoelectric oll-on- water...sensors with coating 12 showed some promise as ammonia vapor sensors. 2. PNP transistor as hydrocarbon vapor sensor; Limited studies have been made

  8. 40 CFR 52.987 - Control of hydrocarbon emissions.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 3 2010-07-01 2010-07-01 false Control of hydrocarbon emissions. 52... (CONTINUED) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Louisiana § 52.987 Control of hydrocarbon... compliance date of January 1, 1980. This shall result in an estimated hydrocarbon emission reduction of...

  9. Urban emissions of water vapor in winter

    Science.gov (United States)

    Salmon, Olivia E.; Shepson, Paul B.; Ren, Xinrong; Marquardt Collow, Allison B.; Miller, Mark A.; Carlton, Annmarie G.; Cambaliza, Maria O. L.; Heimburger, Alexie; Morgan, Kristan L.; Fuentes, Jose D.; Stirm, Brian H.; Grundman, Robert; Dickerson, Russell R.

    2017-09-01

    Elevated water vapor (H2Ov) mole fractions were occasionally observed downwind of Indianapolis, IN, and the Washington, D.C.-Baltimore, MD, area during airborne mass balance experiments conducted during winter months between 2012 and 2015. On days when an urban H2Ov excess signal was observed, H2Ov emission estimates range between 1.6 × 104 and 1.7 × 105 kg s-1 and account for up to 8.4% of the total (background + urban excess) advected flow of atmospheric boundary layer H2Ov from the urban study sites. Estimates of H2Ov emissions from combustion sources and electricity generation facility cooling towers are 1-2 orders of magnitude smaller than the urban H2Ov emission rates estimated from observations. Instances of urban H2Ov enhancement could be a result of differences in snowmelt and evaporation rates within the urban area, due in part to larger wintertime anthropogenic heat flux and land cover differences, relative to surrounding rural areas. More study is needed to understand why the urban H2Ov excess signal is observed on some days, and not others. Radiative transfer modeling indicates that the observed urban enhancements in H2Ov and other greenhouse gas mole fractions contribute only 0.1°C d-1 to the urban heat island at the surface. This integrated warming through the boundary layer is offset by longwave cooling by H2Ov at the top of the boundary layer. While the radiative impacts of urban H2Ov emissions do not meaningfully influence urban heat island intensity, urban H2Ov emissions may have the potential to alter downwind aerosol and cloud properties.

  10. Cesium vapor thermionic converter anomalies arising from negative ion emission

    Energy Technology Data Exchange (ETDEWEB)

    Rasor, Ned S., E-mail: ned.rasor@gmail.com [532 Pauley Woods Circle Kettering, Ohio 45429 (United States)

    2016-08-14

    Compelling experimental evidence is given that a longstanding limit encountered on cesium vapor thermionic energy converter performance improvement and other anomalies arise from thermionic emission of cesium negative ions. It is shown that the energy that characterizes thermionic emission of cesium negative ions is 1.38 eV and, understandably, is not the electron affinity 0.47 eV determined for the photodetachment threshold of the cesium negative ion. The experimental evidence includes measurements of collector work functions and volt-ampere characteristics in quasi-vacuum cesium vapor thermionic diodes, along with reinterpretation of the classic Taylor-Langmuir S-curve data on electron emission in cesium vapor. The quantitative effects of negative ion emission on performance in the ignited, unignited, and quasi-vacuum modes of cesium vapor thermionic converter operation are estimated.

  11. Dynamics of vapor emissions at wire explosion threshold.

    Science.gov (United States)

    Belony, Paul A; Kim, Yong W

    2010-10-01

    X-pinch plasmas have been actively studied in the recent years. Numerical simulation of the ramp-up of metallic vapor emissions from wire specimens shows that under impulsive Ohmic heating the wire core invariably reaches a supercritical state before explosion. The heating rate depends sensitively on the local wire resistance, leading to highly variable vapor emission flux along the wire. To examine the vapor emission process, we have visualized nickel wire explosions by means of shock formation in air. In a single explosion as captured by shadowgraphy, there usually appear several shocks with spherical or cylindrical wave front originating from different parts of the wire. Growth of various shock fronts in time is well characterized by a power-law scaling in one form or another. Continuum emission spectra are obtained and calibrated to measure temperature near the explosion threshold. Shock front structures and vapor plume temperature are examined.

  12. Cesium vapor thermionic converter anomalies arising from negative ion emission

    Science.gov (United States)

    Rasor, Ned S.

    2016-08-01

    Compelling experimental evidence is given that a longstanding limit encountered on cesium vapor thermionic energy converter performance improvement and other anomalies arise from thermionic emission of cesium negative ions. It is shown that the energy that characterizes thermionic emission of cesium negative ions is 1.38 eV and, understandably, is not the electron affinity 0.47 eV determined for the photodetachment threshold of the cesium negative ion. The experimental evidence includes measurements of collector work functions and volt-ampere characteristics in quasi-vacuum cesium vapor thermionic diodes, along with reinterpretation of the classic Taylor-Langmuir S-curve data on electron emission in cesium vapor. The quantitative effects of negative ion emission on performance in the ignited, unignited, and quasi-vacuum modes of cesium vapor thermionic converter operation are estimated.

  13. Investigation of bubble-point vapor pressures for mixtures of an endothermic hydrocarbon fuel with ethanol

    Energy Technology Data Exchange (ETDEWEB)

    Haiyun Sun; Wenjun Fang; Yongsheng Guo; Ruisen Lin [Zhejiang University, Hangzhou (China). Department of Chemistry, Molecular Thermodynamics

    2005-05-01

    Bubble-point vapor pressures and equilibrium temperatures for several mixtures with different mass fractions of a kerosene based endothermic hydrocarbon fuel (EHF) and ethanol were measured by comparative ebulliometry with inclined ebulliometers. Correlation between vapor pressures and equilibrium temperatures by the Antoine equation was given with satisfactory precision. The bubble-point lines of pressure versus composition at different temperatures and temperature versus composition at different pressures were obtained. The pseudo binary systems of EHF+ethanol appear with very large positive deviations from Raoult's law. It follows that the addition of ethanol had a critical effect on the vapor pressure of fuels. Ethanol may be an effective oxygenated hydrocarbon additive to adjust the volatility of EHF. 17 refs., 8 figs., 4 tabs.

  14. Evaluation of Empirical Data and Modeling Studies to Support Soil Vapor Intrusion Screening Criteria for Petroleum Hydrocarbon Compounds

    Science.gov (United States)

    This study is an evaluation of empirical data and select modeling studies of the behavior of petroleum hydrocarbon (PHC) vapors in subsurface soils and how they can affect subsurface-to-indoor air vapor intrusion (VI), henceforth referred to as petroleum vapor intrusion or “PVI” ...

  15. A nonisothermal emissivity and absorptivity formulation for water vapor

    Science.gov (United States)

    Ramanathan, V.; Downey, P.

    1986-01-01

    An emissivity approach is taken to modeling fluxes and cooling rates in the atmosphere. The nonisothermal water vapor long wave radiation emissivity and absorptivity model that is developed satisfies the requirements of defining a monochromatic transfer equation for predicting water vapor emissions. Predictions made with the model compare favorably with fluxes predicted by a radiation model for narrow-band emissions in 5 kayser intervals. The spectral resolution assumed in narrow-band models is shown to be an arbitrary parameter and, if a far wing continuum-type opacity is included in the emissivity scheme presented, results can be obtained which are as accurate as predictions made with state of the art line-by-line (LBL) calculations.

  16. Risk-based evaluation of total petroleum hydrocarbons in vapor intrusion studies.

    Science.gov (United States)

    Brewer, Roger; Nagashima, Josh; Kelley, Michael; Heskett, Marvin; Rigby, Mark

    2013-06-13

    This paper presents a quantitative method for the risk-based evaluation of Total Petroleum Hydrocarbons (TPH) in vapor intrusion investigations. Vapors from petroleum fuels are characterized by a complex mixture of aliphatic and, to a lesser extent, aromatic compounds. These compounds can be measured and described in terms of TPH carbon ranges. Toxicity factors published by USEPA and other parties allow development of risk-based, air and soil vapor screening levels for each carbon range in the same manner as done for individual compounds such as benzene. The relative, carbon range makeup of petroleum vapors can be used to develop weighted, site-specific or generic screening levels for TPH. At some critical ratio of TPH to a targeted, individual compound, the overwhelming proportion of TPH will drive vapor intrusion risk over the individual compound. This is particularly true for vapors associated with diesel and other middle distillate fuels, but can also be the case for low-benzene gasolines or even for high-benzene gasolines if an adequately conservative, target risk is not applied to individually targeted chemicals. This necessitates a re-evaluation of the reliance on benzene and other individual compounds as a stand-alone tool to evaluate vapor intrusion risk associated with petroleum.

  17. Risk-Based Evaluation of Total Petroleum Hydrocarbons in Vapor Intrusion Studies

    Directory of Open Access Journals (Sweden)

    Roger Brewer

    2013-06-01

    Full Text Available This paper presents a quantitative method for the risk-based evaluation of Total Petroleum Hydrocarbons (TPH in vapor intrusion investigations. Vapors from petroleum fuels are characterized by a complex mixture of aliphatic and, to a lesser extent, aromatic compounds. These compounds can be measured and described in terms of TPH carbon ranges. Toxicity factors published by USEPA and other parties allow development of risk-based, air and soil vapor screening levels for each carbon range in the same manner as done for individual compounds such as benzene. The relative, carbon range makeup of petroleum vapors can be used to develop weighted, site-specific or generic screening levels for TPH. At some critical ratio of TPH to a targeted, individual compound, the overwhelming proportion of TPH will drive vapor intrusion risk over the individual compound. This is particularly true for vapors associated with diesel and other middle distillate fuels, but can also be the case for low-benzene gasolines or even for high-benzene gasolines if an adequately conservative, target risk is not applied to individually targeted chemicals. This necessitates a re-evaluation of the reliance on benzene and other individual compounds as a stand-alone tool to evaluate vapor intrusion risk associated with petroleum.

  18. Optimization of gasoline hydrocarbon compositions for reducing exhaust emissions.

    Science.gov (United States)

    Shen, Yitao; Shuai, Shijin; Wang, Jianxin; Xiao, Jianhua

    2009-01-01

    Effects of hydrocarbon compositions on raw exhaust emissions and combustion processes were studied on an engine test bench. The optimization of gasoline hydrocarbon composition was discussed. As olefins content increased from 10.0% to 25.0% in volume, the combustion duration was shortened by about 2 degree crank angle (degrees CA), and the engine-out THC emission was reduced by about 15%. On the other hand, as aromatics content changed from 35.0% to 45.0%, the engine-out NOx emissions increased by 4%. An increment in olefins content resulted in a slight increase in engine-out CO emission, while the aromatics content had little effect on engine-out total hydrocarbon (THC) and CO emissions. Over the new European driving cycle (NEDC), the THC, NOx and CO emissions of fuel with 25.0% olefins and 35.0% aromatics were about 45%, 21% and 19% lower than those of fuel with 10.0% olefins and 40.0% aromatics, respectively. The optimized gasoline compositions for new engines and new vehicles have low aromatics and high olefins contents.

  19. PREVENTION AND CONTROL OF DIMETHYLAMINE VAPORS EMISSION: HERBICIDE PRODUCTION PLANT

    Directory of Open Access Journals (Sweden)

    Zorana Arsenijević

    2008-11-01

    Full Text Available The widely used herbicide, dimethylamine salt of 2,4-dichlorophenoxy acetic acid (2,4-D-DMA, is usually prepared by mixing a dimethylamine (DMA aqueous solution with a solid 2,4-dichlorophenoxy acetic acid (2,4-D. The vapors of the both, reactants and products, are potentially hazardous for the environment. The contribution of DMA vapors in overall pollution from this process is most significant, concerning vapor pressures data of these pollutants. Therefore, the control of the air pollution in the manufacture and handling of methylamines is very important. Within this paper, the optimal air pollution control system in preparation of 2,4-D-DMA was developed for the pesticides manufacturing industry. This study employed the simple pollution prevention concept to reduce the emission of DMA vapors at the source. The investigations were performed on the pilot plant scale. To reduce the emission of DMA vapors, the effluent gases from the herbicide preparation zone were passed through the packed bed scrubber (water - scrubbing medium, and the catalytic reactor in sequence. The end result is a substantially improved air quality in the working area, as well as in the urbanized areas located near the chemical plant.

  20. Prediction of vapor-liquid equilibriafor hydrocarbon binary systems by regular solution model

    OpenAIRE

    下山, 裕介; 米澤, 節子; 小渕, 茂寿; 福地, 賢治; 荒井, 康彦; Shimoyama, Yusuke; Yonezawa, Setsuko; Kobuchi, Shigetoshi; Fukuchi, Kenii; Arai, Yasuhiko

    2007-01-01

    Vapor-liquid equilibria (VLE) of hydrocarbon binary systems : hexane + benzene (25 °C), toluene + octane (60°C) and cyclohexane + toluene (50°C) were predicted by using a regular solution model. In the present model, the mixing entropy term (Flory-Huggins equation) is included and an interaction parameter between unlike molecules is introduced. Solubility parameters and molar volumes at each temperature required in calculation are estimated by previously proposed methods. VLE of hexane + benz...

  1. Piston ring lubrication and hydrocarbon emissions from internal combustion engines

    Energy Technology Data Exchange (ETDEWEB)

    Froelund, K.

    1997-11-01

    Is it the intention with this project to improve the existing hydrocarbon emission model at the Institute by combining it with a model for predicting the piston ring lubrication. The piston ring lubrication model should be experimentally verified to ensure the validity of the model. The following items were the objectives of the current study: Develop a piston ring lubrication model. This implies the development of a ring-pack gas flow model; Examine the response of the piston ring lubrication model to changing engineer conditions. Especially, it would be interesting to look at the engine warm-up phase since this is the phase where the engine-out emissions are highest and where the commonly used three way catalyst is not capable of converting the engine-out emissions, thereby leading the engine-out emissions directly out in to the environment with the exhaust gases; In order to verify the piston ring lubrication model the lubricant distribution on the cylinder liner should be investigated experimentally. Here again it would be of great interesting to look at the engine warm-up phase; The piston ring lubrication model should be adjusted for application together with the new hydrocarbon emission model for SI-engines at the Institute in order to increase the accuracy of the latter; The piston ring lubrication model could be used for describing the transport of PAH`s in diesel engines. (EG)

  2. Hydrocarbon Emission Rings in Protoplanetary Disks Induced by Dust Evolution

    Science.gov (United States)

    Bergin, Edwin A.; Du, Fujun; Cleeves, L. Ilsedore; Blake, G. A.; Schwarz, K.; Visser, R.; Zhang, K.

    2016-11-01

    We report observations of resolved C2H emission rings within the gas-rich protoplanetary disks of TW Hya and DM Tau using the Atacama Large Millimeter Array. In each case the emission ring is found to arise at the edge of the observable disk of millimeter-sized grains (pebbles) traced by submillimeter-wave continuum emission. In addition, we detect a C3H2 emission ring with an identical spatial distribution to C2H in the TW Hya disk. This suggests that these are hydrocarbon rings (i.e., not limited to C2H). Using a detailed thermo-chemical model we show that reproducing the emission from C2H requires a strong UV field and C/O > 1 in the upper disk atmosphere and outer disk, beyond the edge of the pebble disk. This naturally arises in a disk where the ice-coated dust mass is spatially stratified due to the combined effects of coagulation, gravitational settling and drift. This stratification causes the disk surface and outer disk to have a greater permeability to UV photons. Furthermore the concentration of ices that transport key volatile carriers of oxygen and carbon in the midplane, along with photochemical erosion of CO, leads to an elemental C/O ratio that exceeds unity in the UV-dominated disk. Thus the motions of the grains, and not the gas, lead to a rich hydrocarbon chemistry in disk surface layers and in the outer disk midplane.

  3. An Emission Inventory of Polycyclic Aromatic Hydrocarbons in China

    Science.gov (United States)

    Mu, Xilong; Zhu, Xianlei; Wang, Xuesong

    2015-04-01

    Polycyclic Aromatic Hydrocarbons (PAHs) are among the most dangerous compounds due to their high carcinogenic and mutagenic character. Emission inventory provides the primary data to account for the sources of ambient PAHs and server as a necessary database for effective PAHs pollution control. China is experiencing fast economic growth and large energy consumption, which might result in a large amount of PAHs anthropogenic emissions. Therefore, based on the previous studies and combined recently field emission measurements as well as socio-economic activity data, the development of a nationwide PAHs emission inventory is needed. In this work, the emission inventory of 16 PAHs listed as U.S. Environmental Protection Agency priority pollutants in China in the year 2012 is compiled. The emission amounts of PAHs were estimated as annual rates of emission-related activities multiplied by respective emission factors. The activities such as fuel consumption, including fossil fuel and biofuel, and socio-economic statistics were obtained from yearbook released by Chinese central government and/or provincial governments, as well as related industry reports. Emission factors were derived from the related literature. Recently reported emission factors from local measurements were used. The total emissions of PAHs were 120611 ton in 2012. In China, PAHs were emitted predominantly from domestic combustion of coal and biofuel, coking industry and motor vehicles, accounting for 72% of the total amount. PAHs emission profiles were significantly different between China and the other countries. The emission profile in China featured a relatively higher portion of high molecular weight species with carcinogenic potential due to large contributions of domestic combustion and coking industry. Domestic combustion of straw, coal and firewood emitted 19464 ton, 8831 ton, and 5062 ton of PAHs, respectively, which were much higher than those in other countries. Emission per capita showed

  4. Field emission properties of chemical vapor deposited individual graphene

    Energy Technology Data Exchange (ETDEWEB)

    Zamri Yusop, Mohd [Department of Frontier Materials, Nagoya Institute of Technology, Gokiso-cho, Showa-ku, 466-8555 Nagoya (Japan); Department of Materials, Faculty of Mechanical Engineering, Universiti Teknologi Malaysia, 81310 UTM Skudai, Johor (Malaysia); Kalita, Golap, E-mail: kalita.golap@nitech.ac.jp [Department of Frontier Materials, Nagoya Institute of Technology, Gokiso-cho, Showa-ku, 466-8555 Nagoya (Japan); Center for Fostering Young and Innovative Researchers, Nagoya Institute of Technology, Gokiso-cho, Showa-ku, 466-8555 Nagoya (Japan); Yaakob, Yazid; Takahashi, Chisato; Tanemura, Masaki [Department of Frontier Materials, Nagoya Institute of Technology, Gokiso-cho, Showa-ku, 466-8555 Nagoya (Japan)

    2014-03-03

    Here, we report field emission (FE) properties of a chemical vapor deposited individual graphene investigated by in-situ transmission electron microscopy. Free-standing bilayer graphene is mounted on a cathode microprobe and FE processes are investigated varying the vacuum gap of cathode and anode. The threshold field for 10 nA current were found to be 515, 610, and 870 V/μm for vacuum gap of 400, 300, and 200 nm, respectively. It is observed that the structural stability of a high quality bilayer graphene is considerably stable during emission process. By contacting the nanoprobe with graphene and applying a bias voltage, structural deformation and buckling are observed with significant rise in temperature owing to Joule heating effect. The finding can be significant for practical application of graphene related materials in emitter based devices as well as understanding the contact resistance influence and heating effect.

  5. Hydrocarbons emissions from Cerro Prieto Geothermal Power Plant, Mexico

    Science.gov (United States)

    Navarro, Karina; Navarro-González, Rafael; de la Rosa, José; Peralta, Oscar; Castro, Telma; Imaz, Mireya

    2014-05-01

    One of the most important environmental issues related to the use of geothermal fluids to generate electricity is the emission of non-condensable gases to the atmosphere. Mexico has one of the largest geothermal plants in the world. The facility is located at Cerro Prieto, Baja California, roughly 30 km south of Mexicali and the international boundary between Mexico and United States. The Cerro Prieto power plant has 13 units grouped on four individual powerhouses. Gas samples from 9 units of the four powerhouses were collected during 4 campaigns conducted in May-July, 2010, February, 2012, December, 2012, and May, 2013. Gas samples from the stacks were collected in 1000 ml Pyrex round flasks with Teflon stopcocks, and analyzed by gas chromatography-mass spectrometry. Methane was the most abundant aliphatic hydrocarbon, with a concentration that ranged from less than 1% up to 3.5% of the total gas mixture. Normal alkanes represented the second most abundant species, and displayed a decreasing abundance with increasing carbon number in the homologous series. Isoalkanes were also present as isobutane and isopentane. Cycloalkanes occurring as cyclopentane and cyclohexane, were detected only at trace level. Unsaturated hydrocarbons (alkenes and alkynes) were not detected. Benzene was detected at levels ranging from less than 1% up to 3.4% of the total gas mixture. Other aromatic hydrocarbons detected were toluene, and xylenes, and were present at lower concentrations (

  6. An investigation on polycyclic aromatic hydrocarbon emissions from pulverized coal combustion systems

    Science.gov (United States)

    Pisupati; Wasco; Scaroni

    2000-05-29

    Results from a series of tests conducted to study the emission of polynuclear or polycyclic aromatic hydrocarbons (PAHs) from bench-scale and small industrial, water-tube boiler are discussed. A Middle Kittanning, and Upper Freeport seam coals were used in the study. Samples were extracted from the reactor outlet and from the inlet and outlet sides of the research boiler's (RB) baghouse using EPA promulgated methods.Only acenaphthene and fluoranthene were detected in down-fired combustor (DFC) samples. In addition to these two, naphthalene was detected in the RB samples. Emission factors ranged from 80 to 320 &mgr;g/kg of fuel fired. Although there were minor trends in the emissions' data, given the reproducibility limits for PAH compounds, no significant differences were found in the emissions with respect to the fuel type or form (pulverized coal (PC) vs. coal-water slurry fuel (CWSF), and raw vs. cleaned coal) and firing conditions (high and low excess air). The PAH emissions showed a decrease with increase in the firing rate.A bench-scale drop-tube reactor (DTR) was used to study the effects of temperature and residence time on PAH formation. The results revealed near constant PAH concentrations in the solid-phase samples, while the PAH concentrations in the vapor-phase samples increased as a function of temperature. At a temperature of around 1300 degrees C, the rate of PAH formation was exceeded by the rate of PAH oxidation, and PAH concentrations in the vapor phase began to decrease.

  7. Hydrocarbon emission rings in protoplanetary disks induced by dust evolution

    CERN Document Server

    Bergin, Edwin A; Cleeves, L Ilsedore; Blake, Geoffrey A; Schwarz, Kamber; Visser, Ruud; Zhang, Ke

    2016-01-01

    We report observations of resolved C2H emission rings within the gas-rich protoplanetary disks of TW Hya and DM Tau using the Atacama Large Millimeter Array (ALMA). In each case the emission ring is found to arise at the edge of the observable disk of mm-sized grains (pebbles) traced by (sub)mm-wave continuum emission. In addition, we detect a C3H2 emission ring with an identical spatial distribution to C2H in the TW Hya disk. This suggests that these are hydrocarbon rings (i.e. not limited to C2H). Using a detailed thermo-chemical model we show that reproducing the emission from C2H requires a strong UV field and C/O > 1 in the upper disk atmosphere and outer disk, beyond the edge of the pebble disk. This naturally arises in a disk where the ice-coated dust mass is spatially stratified due to the combined effects of coagulation, gravitational settling and drift. This stratification causes the disk surface and outer disk to have a greater permeability to UV photons. Furthermore the concentration of ices that ...

  8. Vapor pressures and sublimation enthalpies of seven heteroatomic aromatic hydrocarbons measured using the Knudsen effusion technique.

    Science.gov (United States)

    Goldfarb, Jillian L; Suuberg, Eric M

    2010-06-01

    The vapor pressures of seven heteroatom-containing cyclic aromatic hydrocarbons, ranging in molecular weight from (168.19 to 208.21) grams plus sign in circlemol(-1) were measured over the temperature range of (301 to 486) Kelvin using the isothermal Knudsen effusion technique. The compounds measured include: anthraquinone, 9-fluorenone, 9-fluorenone oxime, phenoxazine, phenoxathiin and 9H-pyrido[3,4-b]indole. These solid-state sublimation measurements provided values that are compared to vapor pressures of parent aromatic compounds (anthracene and fluorene) and to others with substituent groups in order to examine the effects of alcohol, ketone, pyridine, and pyrrole functionality on this property. The enthalpies and entropies of sublimation for each compound were determined from the Clausius-Clapeyron equation. Though there is no consistent trend in terms of the effects of substitutions on changes in the enthalpy or entropy of sublimation, we note that the prevalence of enthalpic or entropic driving forces on vapor pressure depend on molecule-specific factors and not merely molecular weight of the substituents.

  9. Emission of polycyclic aromatic hydrocarbons from gasohol and ethanol vehicles

    Science.gov (United States)

    de Abrantes, Rui; Vicente de Assunção, João; Pesquero, Célia Regina; Bruns, Roy Edward; Nóbrega, Raimundo Paiva

    The exhaust emission of the polycyclic aromatic hydrocarbons (PAHs) considered toxic to human health were investigated on two spark ignition light duty vehicles, one being gasohol (Gasohol, in Brazil, is the generic denomination for mixtures of pure gasoline plus 20-25% of anhydrous ethyl alcohol fuel (AEAF).)-fuelled and the other a flexible-fuel vehicle fuelled with hydrated ethanol. The influence of fuel type and quality, aged lubricant oil type and use of fuel additives on the formation of these compounds was tested using standardized tests identical to US FTP-75 cycle. PAH sampling and chemical analysis followed the basic recommendations of method TO-13 (United States. Environmental Protection Agency, 1999. Compendium Method TO-13A - Determination of polycyclic Aromatic hydrocarbons (PAH) in Ambient Air Using Gas Chromatography/Mass Spectrometry (CG/MS). Center for environmental research information, Cincinnati, p. 78), with the necessary modification for this particular application. Results showed that the total PAH emission factor varied from 41.9 μg km -1 to 612 μg km -1 in the gasohol vehicle, and from 11.7 μg km -1 to 27.4 μg km -1 in the ethanol-fuelled vehicle, a significant difference in favor of the ethanol vehicle. Generally, emission of light molecular weight PAHs was predominant, while high molecular weights PAHs were not detected. In terms of benzo( a)pyrene toxicity equivalence, emission factors varied from 0.00984 μg TEQ km -1 to 4.61 μg TEQ km -1 for the gasohol vehicle and from 0.0117 μg TEQ km -1 to 0.0218 μg TEQ km -1 in the ethanol vehicle. For the gasohol vehicle, results showed that the use of fuel additive causes a significant increase in the emission of naphthalene and phenanthrene at a confidence level of 90% or higher; the use of rubber solvent on gasohol showed a reduction in the emission of naphthalene and phenanthrene at the same confidence level; the use of synthetic oil instead of mineral oil also contributed

  10. Biogenic nonmethane hydrocarbon emissions estimated from tethered balloon observations

    Science.gov (United States)

    Davis, K. J.; Lenschow, D. H.; Zimmerman, P. R.

    1994-01-01

    A new technique for estimating surface fluxes of trace gases, the mixed-layer gradient technique, is used to calculate isoprene and terpene emissions from forests. The technique is applied to tethered balloon measurements made over the Amazon forest and a pine-oak forest in Alabama at altitudes up to 300 m. The observations were made during the dry season Amazon Boundary Layer Experiment (ABLE 2A) and the Rural Oxidants in the Southern Environment 1990 experiment (ROSE I). Results from large eddy simulations of scalar transport in the clear convective boundary layer are used to infer fluxes from the balloon profiles. Profiles from the Amazon give a mean daytime emission of 3630 +/- 1400 micrograms isoprene sq m/h, where the uncertainty represents the standard deviation of the mean of eight flux estimates. Twenty profiles from Alabama give emissions of 4470 +/- 3300 micrograms isoprene sq m/h, 1740 +/- 1060 micrograms alpha-pinene sq m/h, and 790 +/- 560 micrograms beta-pinene sq m/h, respectively. These results are in agreement with emissions derived from chemical budgets. The emissions may be overestimated because of uncertainty about how to incorporate the effects of the canopy on the mixed-layer gradients. The large variability in these emission estimates is probably due to the relatively short sampling times of the balloon profiles, though spatially heterogeneous emissions may also play a role. Fluxes derived using this technique are representative of an upwind footprint of several kilometers and are independent of hydrocarbon oxidation rate and mean advection.

  11. Frozen Hydrocarbon Particles of Cometary Halos as Carriers of Unidentified Emissions

    Indian Academy of Sciences (India)

    Irakli Simonia

    2005-12-01

    The possible nature of unidentified cometary emissions is under discussion. We propose a new model of the ice particles in cometary halos as a mixture of frozen polycyclic aromatic hydrocarbons and acyclic hydrocarbons.We describe principal properties of frozen hydrocarbon particles (FHPs) and suggest interpreting some of the unidentified cometary emission lines as the photoluminescence of FHPs. The results of comparative analysis are present.

  12. Emissions of non-methane hydrocarbons from cars in China

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    This study investigated the exhaust emission of non-methane hydrocarbons(NMHCs) from cars in China at the Beijing driving cycle on the chassis dynamometer.The emission factor average of NMHCs was 0.9 g/km,which was over twice that from the Australian car fleet and 2-4 times that of the American car emission in the 1990s-2000s.The emission profile of Beijing cars showed higher fractions of aromatics and C4?C7 HCs,and lower percentages of C2?C3 HCs,compared with those of the US car fleet.The average ratio of benzene/toluene for cars tested was 0.5,the average benzene/toluene/ethyl benzene/xylenes(BTEX) ratios were 1/2.2/0.1/1.8,which were consistent with those of the Tanyugou tunnel located in the suburb of Beijing.α-pinene and β-pinene were detected from the exhaust gas on dynamometer for the first time,and had likely similar exhaust emission characteristics with C2?C3 HCs and styrene,giving an evidence that air pinenes may be related to human activities.Isoprene was also detected directly.These observations suggest that the procedure regarding pinenes and isoprene as coming from biologic sources of VOCs in the atmosphere should be applied with great care,especially in the core of the big city like Beijing.The specific reactivity of NMHCs was higher than that of cars of US,and the specific reactivity of volatile aromatic compounds was higher than that of the US SPECIATE database.

  13. Modeling of vapor intrusion from hydrocarbon-contaminated sources accounting for aerobic and anaerobic biodegradation

    Science.gov (United States)

    Verginelli, Iason; Baciocchi, Renato

    2011-11-01

    A one-dimensional steady state vapor intrusion model including both anaerobic and oxygen-limited aerobic biodegradation was developed. The aerobic and anaerobic layer thickness are calculated by stoichiometrically coupling the reactive transport of vapors with oxygen transport and consumption. The model accounts for the different oxygen demand in the subsurface required to sustain the aerobic biodegradation of the compound(s) of concern and for the baseline soil oxygen respiration. In the case of anaerobic reaction under methanogenic conditions, the model accounts for the generation of methane which leads to a further oxygen demand, due to methane oxidation, in the aerobic zone. The model was solved analytically and applied, using representative parameter ranges and values, to identify under which site conditions the attenuation of hydrocarbons migrating into indoor environments is likely to be significant. Simulations were performed assuming a soil contaminated by toluene only, by a BTEX mixture, by Fresh Gasoline and by Weathered Gasoline. The obtained results have shown that for several site conditions oxygen concentration below the building is sufficient to sustain aerobic biodegradation. For these scenarios the aerobic biodegradation is the primary mechanism of attenuation, i.e. anaerobic contribution is negligible and a model accounting just for aerobic biodegradation can be used. On the contrary, in all cases where oxygen is not sufficient to sustain aerobic biodegradation alone (e.g. highly contaminated sources), anaerobic biodegradation can significantly contribute to the overall attenuation depending on the site specific conditions.

  14. Modeling of vapor intrusion from hydrocarbon-contaminated sources accounting for aerobic and anaerobic biodegradation.

    Science.gov (United States)

    Verginelli, Iason; Baciocchi, Renato

    2011-11-01

    A one-dimensional steady state vapor intrusion model including both anaerobic and oxygen-limited aerobic biodegradation was developed. The aerobic and anaerobic layer thickness are calculated by stoichiometrically coupling the reactive transport of vapors with oxygen transport and consumption. The model accounts for the different oxygen demand in the subsurface required to sustain the aerobic biodegradation of the compound(s) of concern and for the baseline soil oxygen respiration. In the case of anaerobic reaction under methanogenic conditions, the model accounts for the generation of methane which leads to a further oxygen demand, due to methane oxidation, in the aerobic zone. The model was solved analytically and applied, using representative parameter ranges and values, to identify under which site conditions the attenuation of hydrocarbons migrating into indoor environments is likely to be significant. Simulations were performed assuming a soil contaminated by toluene only, by a BTEX mixture, by Fresh Gasoline and by Weathered Gasoline. The obtained results have shown that for several site conditions oxygen concentration below the building is sufficient to sustain aerobic biodegradation. For these scenarios the aerobic biodegradation is the primary mechanism of attenuation, i.e. anaerobic contribution is negligible and a model accounting just for aerobic biodegradation can be used. On the contrary, in all cases where oxygen is not sufficient to sustain aerobic biodegradation alone (e.g. highly contaminated sources), anaerobic biodegradation can significantly contribute to the overall attenuation depending on the site specific conditions.

  15. C2-C10 hydrocarbon emissions from a boreal wetland and forest floor

    Directory of Open Access Journals (Sweden)

    H. Hellén

    2006-01-01

    Full Text Available Emissions of various C2-C10 hydrocarbons (VOCs and halogenated hydrocarbons (VHOCs from a boreal wetland and a Scots pine forest floor in south-western Finland were measured by the static chamber technique. Isoprene was the main non-methane hydrocarbon emitted by the wetland, but small emissions of ethene, propane, propene, 1-butene, 2-methylpropene, butane, pentane and hexane were also detected. The isoprene emission from the wetland was observed to follow the commonly-used isoprene emission algorithm. The mean emission potential of isoprene was 224 µg m-2 h-1 for the whole season. This is lower than the emission potentials published earlier; that is probably at least partly due to the cold and cloudy weather during the measurements. No emissions were detected of monoterpenes or halogenated hydrocarbons from the wetland. The highest hydrocarbon emissions from the Scots pine forest floor were measured in spring and autumn. However, only a few measurements were conducted during summer. The main compounds emitted were monoterpenes. Isoprene emissions were negligible. The total monoterpene emission rates varied from zero to 373 µg m-2 h-1. The results indicated that decaying plant litter may be the source for these emissions. Small emissions of chloroform (100-800 ng m-2 h-1, ethene, propane, propene, 2-methylpropene, cis-2-butene, pentane, hexane and heptane were detected. Comparison with Scots pine emissions showed that the forest floor may be an important monoterpene source, especially in spring.

  16. Phosphorescence emission and excited states of 3- and 4-hydroxybenzaldehyde vapors

    Science.gov (United States)

    Itoh, Takao

    2014-01-01

    Emission spectra of 3- and 4-hydroxybenzaldehyde vapors have been measured along with the excitation and absorption spectra. It is inferred from the temperature dependence of the phosphorescence spectrum that the phosphorescence of 4-hydroxybenzaldehyde vapor originates from the T2(n, π*) state. In the case of 3-hydroxybenzaldehyde vapor, the emission is shown to consist of that of 3-hydroxybenzaldehyde and benzaldehyde vapors, with the latter molecule being generated as the result of photochemical decomposition of 3-hydroxybenzaldehyde. The interpretation of the emission spectrum of 3-hydroxybenzaldehyde is different from that reported previously. The rotational isomer responsible for appearance of the phosphorescence of 3-hydroxybenzaldehyde vapor is suggested based on DFT calculation and emission spectral data.

  17. Emissions of polycyclic aromatic hydrocarbons from coking industries in China

    Institute of Scientific and Technical Information of China (English)

    Ling Mu; Lin Peng; Junji Cao; Qiusheng He; Fan Li; Jianqiang Zhang; Xiaofeng Liu

    2013-01-01

    This study set out to assess the characteristics of polycyclic aromatic hydrocarbon (PAH) emission from coking industries,with field samplings conducted at four typical coke plants.For each selected plant,stack flue gas samples were collected during processes that included charging coal into the ovens (CC),pushing coke (PC) and the combustion of coke-oven gas (CG).Sixteen individual PAHs on the US EPA priority list were analyzed by gas chromatography/mass spectrometry (GC/MS).Results showed that the total PAH concentrations in the flue gas ranged from 45.776 to 414.874 μg/m3,with the highest emission level for CC (359.545 μg/m3).The concentration of PAH emitted from the CC process in CP1 (stamp charging) was lower than that from CP3 and CP4 (top charging).Low-molecular-weight PAHs (i.e.,two-to three-ring PAHs) were predominant contributors to the total PAH contents,and Nap,AcPy,Flu,PhA,and AnT were found to be the most abundant ones.Total BaPeq concentrations for CC (2.248 iμg/m3) were higher than those for PC (1.838 μg/m3) and CG (1.082 μg/m3),and DbA was an important contributor to carcinogenic risk as BaP in emissions from coking processes.Particulate PAH accounted for more than 20% of the total BaPeq concentrations,which were significantly higher than the corresponding contributions to the total PAH mass concentration (5%).Both particulate and gaseous PAH should be taken into consideration when the potential toxicity risk of PAH pollution during coking processes is assessed.The mean total-PAH emission factors were 346.132 and 93.173 μg/kg for CC and PC,respectively.

  18. A Review on Prediction Methods for Molar Enthalpies of Vaporization of Hydrocarbons: The ELBA Method as the Best Answer

    Science.gov (United States)

    Santos, Rui C.; Leal, João P.

    2012-12-01

    A review on prediction methods for molar enthalpies of vaporization at T = 298.15 K of hydrocarbons is presented. A new method is proposed and compared with six of the most common used ones from the literature. This new method, the extended Laidler bond additivity (ELBA), was applied to the prediction of standard molar enthalpies of vaporization of hydrocarbons (alkanes, alkenes, alkynes, polyenes, poly-ynes, cycloalkanes, cycloalkenes, benzene compounds, biphenyl compounds, and polyphenyl compounds) at T = 298.15 K. A total of 260 experimental standard molar enthalpies of vaporization at T = 298.15 K were used for the parameters optimization. Comparison between the experimental values and those calculated using ELBA led to an average absolute difference of 0.35 kJ mol-1, corresponding to an average relative error of 0.92%. In addition, this new method proves to be better than the ones used for comparison with an independent set of 83 experimental standard molar enthalpies of vaporization at T = 298.15 K.

  19. Theoretical modeling of infrared emission from neutral and charged polycyclic aromatic hydrocarbons. II.

    NARCIS (Netherlands)

    Bakes, ELO; Tielens, AGGM; Bauschlicher, CW; Hudgins, DM; Allamandola, LJ

    2001-01-01

    The nature of the carriers of the interstellar infrared (IR) emission features between 3.3 and 12.7 mum is complex. We must consider emission from a family of polycyclic aromatic hydrocarbons (PAHs) in a multiplicity of cationic charge states (+1, +2, +3, and so on), along with neutral and anionic P

  20. Developing Mathematical Provisions for Assessment of Liquid Hydrocarbon Emissions in Emergency Situations

    Science.gov (United States)

    Zemenkova, M. Yu; Zemenkov, Yu D.; Shantarin, V. D.

    2016-10-01

    The paper reviews the development of methodology for calculation of hydrocarbon emissions during seepage and evaporation to monitor the reliability and safety of hydrocarbon storage and transportation. The authors have analyzed existing methods, models and techniques for assessing the amount of evaporated oil. Models used for predicting the material balance of multicomponent two-phase systems have been discussed. The results of modeling the open-air hydrocarbon evaporation from an oil spill are provided and exemplified by an emergency pit. Dependences and systems of differential equations have been obtained to assess parameters of mass transfer from the open surface of a liquid multicomponent mixture.

  1. THE RATES OF POLYCYCLIC AROMATIC HYDROCARBON EMISSIONS FROM INCENSE BURNING

    Science.gov (United States)

    The paper presents the results of experiments performed to determine the amounts of gas- and particle-phase polycyclic aromatic hydrocarbons (PAHS) in incense smoke. Ten brands of incense, 3 of stick, 2 of joss stick, and one each of cone, smudge bundle, rope, powder, and rock, w...

  2. Stimulated emission of ultraviolet radiation by vapors of complex molecules

    Energy Technology Data Exchange (ETDEWEB)

    Barkova, L.A.; Gruzinskii, V.V.; Danilova, V.I.; Degtyarenko, K.M.; Kopylova, T.N.; Kuznetsov, A.L.

    1981-08-01

    Lasing was observed in vapors of new organic compounds: para-terphenyl, 2-phenylbenzoxazole, 2-(n-tolyl) benzoxazole, 2-(n-methoxyphenyl) benzoxazole, 2-(n-dimethylaminophenyl) benzoxazole, 2-biphenylbenzoxazole, 2-(..cap alpha..-naphthyl) benzoxazole, and also 1,4-di(n-phenylethynyl) benzole, and para-quaterphenyl pumped transversely by XeCl excimer laser radiation at lambda/sub p/ = 308 nm. The lasing bands without tuning covered the 330--370 nm range. The shortest-wavelength maximum (333.5 nm) was observed for 2-(n-methoxyphenyl) benzoxazole. An analysis was made of the lasing ability of the molecules.

  3. Hydrocarbon emissions from gas engine CHP-units. 2011 measurement program

    Energy Technology Data Exchange (ETDEWEB)

    Van Dijk, G.H.J. [KEMA, Arnhem (Netherlands)

    2012-06-15

    In December 2009, the Ministry of Infrastructure and Environment (IandM) issued the Decree on Emission Limits for Middle Sized Combustion Installations (BEMS). This decree imposes a first-time emission limit value (ELV) of 1500 mg C/m{sup 3}{sub o} at 3% O{sub 2} for hydrocarbons emitted by gas engines. IandM used the findings of two hydrocarbon emission measurement programs, executed in 2007 and 2009, as a guideline for this initial ELV. The programs did reveal substantial variation in the hydrocarbon emissions of the gas engines tested. This variation, and especially the uncertainty as to the role of engine and/or other parameters causing such variation, was felt to hamper further policy development. IandM therefore commissioned KEMA to perform follow-up measurements on ten gas engine CHP-units in 2011. Aim of this 2011 program is to assess hydrocarbon emission variation in relation to engine parameters and process conditions including maintenance status, and to atmospheric conditions. The 2011 program comprised two identical measurement sessions, one in spring and one in winter.

  4. Quantitative relationships for the prediction of the vapor pressure of some hydrocarbons from the van der Waals molecular surface

    Directory of Open Access Journals (Sweden)

    Olariu Tudor

    2015-01-01

    Full Text Available A quantitative structure - property relationship (QSPR modeling of vapor pressure at 298.15 K, expressed as log (VP / Pa was performed for a series of 84 hydrocarbons (63 alkanes and 21 cycloalkanes using the van der Waals (vdW surface area, SW/Å2, calculated by the Monte Carlo method, as the molecular descriptor. The QSPR model developed from the subset of 63 alkanes (C1-C16, deemed as the training set, was successfully used for the prediction of the log (VP / Pa values of the 21 cycloalkanes, which was the external prediction (test subset. A QSPR model was also developed for a series composed of all 84 hydrocarbons. Both QSPR models were statistically tested for their ability to fit the data and for prediction. The results showed that the vdW molecular surface used as molecular descriptor (MD explains the variance of the majority of the log (VP / Pa values in this series of 84 hydrocarbons. This MD describes very well the intermolecular forces that hold neutral molecules together. The clear physical meaning of the molecular surface values, SW/Å2, could explain the success of the QSPR models obtained with a single structural molecular descriptor.

  5. Use of dissolved and vapor-phase gases to investigate methanogenic degradation of petroleum hydrocarbon contamination in the subsurface

    Science.gov (United States)

    Amos, R.T.; Mayer, K.U.; Bekins, B.A.; Delin, G.N.; Williams, R.L.

    2005-01-01

    [1] At many sites contaminated with petroleum hydrocarbons, methanogenesis is a significant degradation pathway. Techniques to estimate CH4 production, consumption, and transport processes are needed to understand the geochemical system, provide a complete carbon mass balance, and quantify the hydrocarbon degradation rate. Dissolved and vapor-phase gas data collected at a petroleum hydrocarbon contaminated site near Bemidji, Minnesota, demonstrate that naturally occurring nonreactive or relatively inert gases such as Ar and N2 can be effectively used to better understand and quantify physical and chemical processes related to methanogenic activity in the subsurface. In the vadose zone, regions of Ar and N2 depletion and enrichment are indicative of methanogenic and methanotrophic zones, and concentration gradients between the regions suggest that reaction-induced advection can be an important gas transport process. In the saturated zone, dissolved Ar and N2 concentrations are used to quantify degassing driven by methanogenesis and also suggest that attenuation of methane along the flow path, into the downgradient aquifer, is largely controlled by physical processes. Slight but discernable preferential depletion of N2 over Ar, in both the saturated and unsaturated zones near the free-phase oil, suggests reactivity of N2 and is consistent with other evidence indicating that nitrogen fixation by microbial activity is taking place at this site. Copyright 2005 by the American Geophysical Union.

  6. Hydrocarbons Emissions Due to Wellbore and other Subsurface Leakage in the Uintah Basin, Utah

    Science.gov (United States)

    Watkins, C.; Lyman, S. N.

    2015-12-01

    The explosive growth of oil and gas production in the United States has focused public and regulatory attention on environmental impacts of hydrocarbon extraction, including air quality and climate impacts. One potentially important emissions source is subsurface leakage of natural gas. Better understanding of wellbore and other subsurface leaks are important in providing ways to decrease pollution while increasing the efficiency of oil and gas production. Soil gas measurements carried out by USGS over the last several years in Utah's oil and gas fields have shown that, while concentrations of methane in soils near wells are typically low, soil gas near some wells can contain more than 50% methane. In the summers of 2013-2015 we carried out campaigns to measure the emission rate of methane and other hydrocarbons from soils near wells in the Uintah Basin, Utah. We also measured emissions at several locations on individual well pads and determined that concentrations of hydrocarbons tend to decrease with distance from the well head. Soil emissions were also measured at non-well sites in the same area to determine background emission rates. Emissions from exposed coal, oil shale, gilsonite, and fault zone surfaces were also measured. Relationships of emissions with soil gas concentrations, meteorological conditions, and soil properties were also investigated.

  7. An Approach that Uses the Concentrations of Hydrocarbon Compounds in Soil Gas at the Source of Contamination to Evaluate the Potential for Intrusion of Petroleum Vapors into Buildings (PVI)

    Science.gov (United States)

    If motor fuels are spilled from underground storage tanks, petroleum hydrocarbons can vaporize from the spill and move as a vapor through the unsaturated zone. If a building is sited above or near the spill, the hydrocarbons may intrude into the air space of the building. This ...

  8. An Approach that Uses the Concentrations of Hydrocarbon Compounds in Soil Gas at the Source of Contamination to Evaluate the Potential for Intrusion of Petroleum Vapors into Buildings (PVI)

    Science.gov (United States)

    If motor fuels are spilled from underground storage tanks, petroleum hydrocarbons can vaporize from the spill and move as a vapor through the unsaturated zone. If a building is sited above or near the spill, the hydrocarbons may intrude into the air space of the building. This ...

  9. Estimated IR and phosphorescence emission fluxes for specific Polycyclic Aromatic Hydrocarbons in the Red Rectangle

    CERN Document Server

    Mulas, G; Joblin, C; Toublanc, D

    2005-01-01

    Following the tentative identification of the blue luminescence in the Red Rectangle by Vijh et al. (2005), we compute absolute fluxes for the vibrational IR emission and phosphorescence bands of three small polycyclic aromatic hydrocarbons. The calculated IR spectra are compared with available ISO observations. A subset of the emission bands are predicted to be observable using presently available facilities, and can be used for an immediate, independent, discriminating test on their alleged presence in this well-known astronomical object.

  10. Emissions of Parent, Nitro, and Oxygenated Polycyclic Aromatic Hydrocarbons from Residential Wood Combustion in Rural China

    OpenAIRE

    SHEN, Guofeng; TAO, SHU; WEI, Siye; ZHANG, Yanyan; Wang, Rong; Wang, Bin; Li, Wei; Shen, Huizhong; HUANG, YE; Chen, Yuanchen; Chen, Han; Yang, Yifeng; Wang, Wei; Wang, Xilong; Liu, Wenxin

    2012-01-01

    Residential wood combustion is one of the important sources of air pollution in developing countries. Among the pollutants emitted, parent polycyclic aromatic hydrocarbons (pPAHs) and their derivatives, including nitrated and oxygenated PAHs (nPAHs and oPAHs), are of concern because of their mutagenic and carcinogenic effects. In order to evaluate their impacts on regional air quality and human health, emission inventories, based on realistic emission factors (EFs), are needed. In this study,...

  11. Hydrogen sulfide and nonmethane hydrocarbon emissions from broiler houses in the Southeastern United States

    Science.gov (United States)

    Hydrogen sulfide (H2S) and nonmethane hydrocarbon (NMHC) emissions from two mechanically ventilated commercial broiler houses located in the Southeastern United States were continuously monitored over 12 flocks during the one-year period of 2006-2007 as a joint effort between Iowa State University a...

  12. Nitrous oxide emissions in a membrane bioreactor treating saline wastewater contaminated by hydrocarbons.

    Science.gov (United States)

    Mannina, Giorgio; Cosenza, Alida; Di Trapani, Daniele; Laudicina, Vito Armando; Morici, Claudia; Ødegaard, Hallvard

    2016-11-01

    The joint effect of wastewater salinity and hydrocarbons on nitrous oxide emission was investigated. The membrane bioreactor pilot plant was operated with two phases: i. biomass acclimation by increasing salinity from 10gNaClL(-1) to 20gNaClL(-1) (Phase I); ii. hydrocarbons dosing at 20mgL(-1) with a constant salt concentration of 20gNaClL(-1) (Phase II). The Phase I revealed a relationship between nitrous oxide emissions and salinity. During the end of the Phase I, the activity of nitrifiers started to recover, indicating a partial acclimatization. During the Phase II, the hydrocarbon shock induced a temporary inhibition of the biomass with the suppression of nitrous oxide emissions. The results revealed that the oxic tank was the major source of nitrous oxide emission, likely due to the gas stripping by aeration. The joint effect of salinity and hydrocarbons was found to be crucial for the production of nitrous oxide.

  13. THE GEOLOGICAL CONDITIONING OF HYDROCARBON EMISSIONS RESULTING FROM SOIL CONTAMINATION

    Directory of Open Access Journals (Sweden)

    Ewa J. Lipińska

    2014-12-01

    Full Text Available Synchronization economy of oil mining and mineral waters is associated with planning the functions of spa treatment. Environmental protection of the spa areas also applies to preserve their technical and cultural heritage. This article attempts to determine the places of natural and anthropogenic hydrocarbon pollution substances. Their presence in the soil affects the quality of the environment. As a result, maps are produced showing directions of research: (1 the natural background of biodiversity, and (2 potential anthropogenic pollution. They are assessed in the context of the health and human life, protection of the environment and the possibility of damage to the environment. Research is conducted in communes of the status of the spa – for special protection.

  14. Investigation on Methane Decomposition and the Formation of C2 Hydrocarbons in DC Discharge Plasma byEmission Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    贺建勋; 韩媛媛; 高爱华; 周引穗; 陆治国

    2004-01-01

    The IR emission spectra of methane were measured under DC glow discharge conditions. The distinct difference in time between methane decomposition and C2 hydrocarbons formation was specially pointed out. C2 hydrocarbons formed at the end of methane decomposition. The optimum condition for C2 hydrocarbon formation was studied and the optimum combination between electric current density and methane input quantity was suggested. The appropriate reaction conditions for methane decomposition and C2 hydrocarbons formation are different, so high yield of C2 hydrocarbons will be probably obtained when different conditions are taken.

  15. Mesospheric water vapor sounding using earth-limb pure-rotational emission in the LWIR

    Science.gov (United States)

    Adler-Golden, Steven; de, Piali; Smith, Donald; D'Agati, Anthony

    1993-08-01

    Limb sounding of mesospheric water vapor using pure rotational emission in the long-wavelength IR region has been demonstrated using data from the ELC-1 rocket experiment, launched in October, 1983. By simultaneously analyzing H2O emission at 23-29 microns and CO2 emission in the nu2 band region, effects due to uncertainties in the atmospheric temperature and instrument calibration are minimized. The H2O profile obtained from ELC-1 is consistent with other fall to early-winter measurements. Given accurate line-of-sight pointing information, this approach will be feasible for global mesospheric H2O sounding from limb-viewing satellites.

  16. Using Concentrations of Methane and Gasoline Hydrocarbons in Soil Gas to Predict Vapor Intrusion of Benzene

    Science.gov (United States)

    Risk management of petroleum vapor intrusion has been a daunting and challenging task for the Underground Storage Tank Program. Because chlorinated solvents do not degrade in soil gas, techniques that focus on their properties and behavior can produce useful estimates. However, t...

  17. ANALYSIS OF HYDROCARBON TREATING SYSTEM TO THE EMISSION OFF SPARK-IGNITION FOUR-STROKE ENGINE

    Directory of Open Access Journals (Sweden)

    Binyamin Binyamin

    2016-08-01

    Full Text Available The reduction of carbon monoxide (CO, unburnthydrocarbon (UHC emission and fuel consumption on spark-ignition four-stroke engine is continuously attempted. The purposes from this research were to determine the effect of Hydrocarbon Treating System (HTS  on levels of CO, UHC and fuel consumption. This is an experimental research. Its is conducted by comparing the exhaust pollutant concentration such as carbon monoxide, unburnt hydrocarbon and also fuel consumption between standard engine setting and Hydrocarbon Treating System applied. The research variable are HTS flow rate from Q1 = 0 cc/s (without HTS, Q2 = 1,5 cc/s, Q3 = 2 cc/s, Q4 = 2,5 cc/s, and Q5 = 33 cc/s. The research will be done in three conditions which are low, medium and high rotation. The result showed that Hydrocarbon Threating System decrease fuel consumption up to 19,43% with flow rate Q5 = 3 cc/s, but on the other hand it increase CO emission up to 80.84% with flow rate Q5 = 3 cc/s and UHC emission level up to 124.75% with flow rate Q5 = 3 cc/s from engine standart condition.

  18. Improving Dryer and Press Efficiencies Through Combustion of Hydrocarbon Emissions

    Energy Technology Data Exchange (ETDEWEB)

    Sujit Banerjee

    2005-10-31

    Emission control devices on dryers and presses have been legislated into the industry, and are now an integral part of the drying system. These devices consume large quantities of natural gas and electricity and down-sizing or eliminating them will provide major energy savings. The principal strategy taken here focuses on developing process changes that should minimize (and in some cases eliminate) the need for controls. A second approach is to develop lower-cost control options. It has been shown in laboratory and full-scale work that Hazardous Air Pollutants (HAPs) emerge mainly at the end of the press cycle for particleboard, and, by extension, to other prod-ucts. Hence, only the air associated with this point of the cycle need be captured and treated. A model for estimating terpene emissions in the various zones of veneer dryers has been developed. This should allow the emissions to be concentrated in some zones and minimized in others, so that some of the air could be directly released without controls. Low-cost catalysts have been developed for controlling HAPs from dryers and presses. Catalysts conventionally used for regenerative catalytic oxidizers can be used at much lower temperatures for treating press emissions. Fluidized wood ash is an especially inexpensive mate-rial for efficiently reducing formaldehyde in dryer emissions. A heat transfer model for estimating pinene emissions from hot-pressing strand for the manufacture of flakeboard has been constructed from first principles and validated. The model shows that most of the emissions originate from the 1-mm layer of wood adjoining the platen surface. Hence, a simple control option is to surface a softwood mat with a layer of hardwood prior to pressing. Fines release a disproportionate large quantity of HAPs, and it has been shown both theo-retically and in full-scale work that particles smaller than 400 µm are principally responsible. Georgia-Pacific is considering green

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-07-01

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

  20. Prediction of cold start hydrocarbon emissions of air cooled two wheeler spark ignition engines by simple fuzzy logic simulation

    Directory of Open Access Journals (Sweden)

    Samuel Raja Ayyanan

    2014-01-01

    Full Text Available The cold start hydrocarbon emission from the increasing population of two wheelers in countries like India is one of the research issues to be addressed. This work describes the prediction of cold start hydrocarbon emissions from air cooled spark ignition engines through fuzzy logic technique. Hydrocarbon emissions were experimentally measured from test engines of different cubic capacity, at different lubricating oil temperature and at different idling speeds with and without secondary air supply in exhaust. The experimental data were used as input for modeling average hydrocarbon emissions for 180 seconds counted from cold start and warm start of gasoline bike engines. In fuzzy logic simulation, member functions were assigned for input variables (cubic capacity and idling rpm and output variables (average hydrocarbon emission for first 180 seconds at cold start and warm start. The knowledge based rules were adopted from the analyzed experimental data and separate simulations were carried out for predicting hydrocarbon emissions from engines equipped with and without secondary air supply. The simulation yielded the average hydrocarbon emissions of air cooled gasoline engine for a set of given input data with accuracy over 90%.

  1. Biomass Conversion to Produce Hydrocarbon Liquid Fuel Via Hot-vapor Filtered Fast Pyrolysis and Catalytic Hydrotreating.

    Science.gov (United States)

    Wang, Huamin; Elliott, Douglas C; French, Richard J; Deutch, Steve; Iisa, Kristiina

    2016-12-25

    Lignocellulosic biomass conversion to produce biofuels has received significant attention because of the quest for a replacement for fossil fuels. Among the various thermochemical and biochemical routes, fast pyrolysis followed by catalytic hydrotreating is considered to be a promising near-term opportunity. This paper reports on experimental methods used 1) at the National Renewable Energy Laboratory (NREL) for fast pyrolysis of lignocellulosic biomass to produce bio-oils in a fluidized-bed reactor and 2) at Pacific Northwest National Laboratory (PNNL) for catalytic hydrotreating of bio-oils in a two-stage, fixed-bed, continuous-flow catalytic reactor. The configurations of the reactor systems, the operating procedures, and the processing and analysis of feedstocks, bio-oils, and biofuels are described in detail in this paper. We also demonstrate hot-vapor filtration during fast pyrolysis to remove fine char particles and inorganic contaminants from bio-oil. Representative results showed successful conversion of biomass feedstocks to fuel-range hydrocarbon biofuels and, specifically, the effect of hot-vapor filtration on bio-oil production and upgrading. The protocols provided in this report could help to generate rigorous and reliable data for biomass pyrolysis and bio-oil hydrotreating research.

  2. Estimates for biogenic non-methane hydrocarbons and nitric oxide emissions in the Valley of Mexico

    Science.gov (United States)

    Velasco, Erik

    Biogenic non-methane hydrocarbons (NMHC), 2-methyl-3-buten-2-ol (methylbutenol or MBO) and nitrogen oxide (NO) emissions were estimated for the Valley of Mexico developing a spatially and temporally resolved emission inventory for air quality models. The modeling domain includes all the Metropolitan Mexico City Area, the surrounding forests and agriculture fields. The estimates were based on several sources of land use and land cover data and a biogenic emission model; the biomass density and tree characteristics were obtained from reforestation program data. The biogenic emissions depend also on climatic conditions, mainly temperature and solar radiation. The temperature was obtained from a statistical revision of the last 10 yr data reported by the Mexico City Automatic Atmospheric Monitoring Network, while the solar radiation data were obtained from measurements performed in a typical oak forest in the Valley and from sources of total solar radiation data for Mexico City. The results indicated that 7% of total hydrocarbon emissions in Mexico Valley are due to vegetation and NO emissions from soil contribute with 1% to the total NO x emissions.

  3. Measurements of hydrocarbons, oxygenated hydrocarbons, carbon monoxide, and nitrogen oxides in an urban basin in Colorado: Implications for Emission Inventories

    Science.gov (United States)

    Goldan, P. D.; Trainer, M.; Kuster, W. C.; Parrish, D. D.; Carpenter, J.; Roberts, J. M.; Yee, J. E.; Fehsenfeld, F. C.

    1995-11-01

    Concentrations of a wide variety of volatile organic compounds (VOCs) in the C3 to C10 range, CO, NOy (total reactive oxidized nitrogen), SO2, and meteorological parameters were measured concurrently at a site on the western perimeter of Boulder, Colorado, during February 1991. The measurement site, located some 150 m above the Boulder urban basin, receives air masses typifying averaged local sources. The highest hydrocarbon concentrations observed showed little effects of photochemical loss processes and reflect the pattern of the local emission sources. The observed ratios of CO and the VOCs to NOy are compared to those predicted by the 1985 National Acid Precipitation Assessment Program (NAPAP) inventory.These comparisons indicate (1) good agreement for CO/NOY, (2) significant overpredictions by the NAPAP inventory for many of the hydrocarbon to NOY ratios, (3) much more benzene from mobile sources (and less from area sources) than predicted by the NAPAP inventory, and (4) large underpredictions of the light alcohols and carbonyls by the NAPAP inventory. These first two results are in marked contrast to the conclusions of the recent tunnel study reported by Ingalls in 1989. Source profile reconciliation implies substantial input from both a local propane source and gasoline headspace venting.

  4. Petroleum Vapor Intrusion

    Science.gov (United States)

    One type of vapor intrusion is PVI, in which vapors from petroleum hydrocarbons such as gasoline, diesel, or jet fuel enter a building. Intrusion of contaminant vapors into indoor spaces is of concern.

  5. Method of treating emissions of a hybrid vehicle with a hydrocarbon absorber and a catalyst bypass system

    Science.gov (United States)

    Roos, Bryan Nathaniel; Gonze, Eugene V; Santoso, Halim G; Spohn, Brian L

    2014-01-14

    A method of treating emissions from an internal combustion engine of a hybrid vehicle includes directing a flow of air created by the internal combustion engine when the internal combustion engine is spinning but not being fueled through a hydrocarbon absorber to collect hydrocarbons within the flow of air. When the hydrocarbon absorber is full and unable to collect additional hydrocarbons, the flow of air is directed through an electrically heated catalyst to treat the flow of air and remove the hydrocarbons. When the hydrocarbon absorber is not full and able to collect additional hydrocarbons, the flow of air is directed through a bypass path that bypasses the electrically heated catalyst to conserve the thermal energy stored within the electrically heated catalyst.

  6. Compilation of a source profile database for hydrocarbon and OVOC emissions in China

    Science.gov (United States)

    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.

  7. The relationship between polycyclic aromatic hydrocarbon emission and far-infrared dust emission from NGC 2403 and M83

    CERN Document Server

    Jones, A G; Baes, M; Boquien, M; Boselli, A; De Looze, I; Fritz, J; Galliano, F; Hughes, T M; Lebouteiller, V; Lu, N; Madden, S C; Remy-Ruyer, A; Smith, M W L; Spinoglio, L; Zijlstra, A A

    2014-01-01

    We examine the relation between polycyclic aromatic hydrocarbon (PAH) emission at 8 microns and far-infrared emission from hot dust grains at 24 microns and from large dust grains at 160 and 250 microns in the nearby spiral galaxies NGC 2403 and M83 using data from the Spitzer Space Telescope and Herschel Space Observatory. We find that the PAH emission in NGC 2403 is better correlated with emission at 250 microns from dust heated by the diffuse interstellar radiation field (ISRF) and that the 8/250 micron surface brightness ratio is well-correlated with the stellar surface brightness as measured at 3.6 microns. This implies that the PAHs in NGC 2403 are intermixed with cold large dust grains in the diffuse interstellar medium (ISM) and that the PAHs are excited by the diffuse ISRF. In M83, the PAH emission appears more strongly correlated with 160 micron emission originating from large dust grains heated by star forming regions. However, the PAH emission in M83 is low where the 24 micron emission peaks withi...

  8. Characterization of hydrocarbon emissions from green sand foundry core binders by analytical pyrolysis

    Energy Technology Data Exchange (ETDEWEB)

    Yujue Wang; Fred S. Cannon; Magda Salama; Jeff Goudzwaard; James C. Furness [Pennsylvania State University, University Park, PA (United States). Department of Civil and Environmental Engineering

    2007-11-15

    Analytical pyrolysis was conducted to compare the hydrocarbon and greenhouse gas emissions of three foundry sand binders: (a) conventional phenolic urethane resin, (b) biodiesel phenolic urethane resin, and (c) collagen-based binder. These binders are used in the metal casting industry to create internal cavities within castings. Green sand contains silica sand, clay, carbonaceous additives (eg bituminous coal) and water. The core samples were flash pyrolyzed in a Curie-point pyrolyzer at 920{sup o}C with a heating rate of about 3000{sup o}C/sec. This simulated some key features of the fast heating conditions that the core binders would experience at the metal-core interface when molten metal is poured into green sand molds. The core samples were also pyrolyzed in a thermogravimetric analyzer (TGA) from ambient temperature to 1000{sup o}C with a heating rate of 30{sup o}C/min, and this simulated key features of the slow heating conditions that the core binders would experience at distances that are further away from the metal-core interface during casting cooling. Hydrocarbon emissions from flash pyrolysis were analyzed with a gas chromatography-flame ionization detector, while hydrocarbon and greenhouse gas emissions from TGA pyrolysis were monitored with mass spectrometry. The prominent hazardous air pollutant emissions during pyrolysis of the three binders were phenol, cresols, benzene, and toluene for the conventional phenolic urethane resin and biodiesel resin, and benzene and toluene for the collagen-based binder. Bench-scale analytical pyrolysis techniques could be a useful screening tool for the foundries to compare the relative emissions of alternative core binders and to choose proper materials in order to comply with air-emission regulations. 20 refs., 4 figs., 1 tab.

  9. Novel techniques for characterization of hydrocarbon emission sources in the Barnett Shale

    Science.gov (United States)

    Nathan, Brian Joseph

    Changes in ambient atmospheric hydrocarbon concentrations can have both short-term and long-term effects on the atmosphere and on human health. Thus, accurate characterization of emissions sources is critically important. The recent boom in shale gas production has led to an increase in hydrocarbon emissions from associated processes, though the exact extent is uncertain. As an original quantification technique, a model airplane equipped with a specially-designed, open-path methane sensor was flown multiple times over a natural gas compressor station in the Barnett Shale in October 2013. A linear optimization was introduced to a standard Gaussian plume model in an effort to determine the most probable emission rate coming from the station. This is shown to be a suitable approach given an ideal source with a single, central plume. Separately, an analysis was performed to characterize the nonmethane hydrocarbons in the Barnett during the same period. Starting with ambient hourly concentration measurements of forty-six hydrocarbon species, Lagrangian air parcel trajectories were implemented in a meteorological model to extend the resolution of these measurements and achieve domain-fillings of the region for the period of interest. A self-organizing map (a type of unsupervised classification) was then utilized to reduce the dimensionality of the total multivariate set of grids into characteristic one-dimensional signatures. By also introducing a self-organizing map classification of the contemporary wind measurements, the spatial hydrocarbon characterizations are analyzed for periods with similar wind conditions. The accuracy of the classification is verified through assessment of observed spatial mixing ratio enhancements of key species, through site-comparisons with a related long-term study, and through a random forest analysis (an ensemble learning method of supervised classification) to determine the most important species for defining key classes. The hydrocarbon

  10. Global atmospheric emission inventory of polycyclic aromatic hydrocarbons (PAHs) for 2004

    Science.gov (United States)

    Zhang, Yanxu; Tao, Shu

    The global atmospheric emissions of the 16 polycyclic aromatic hydrocarbons (PAHs) listed as the US EPA priority pollutants were estimated using reported emission activity and emission factor data for the reference year 2004. A database for emission factors was compiled, and their geometric means and frequency distributions applied for emission calculation and uncertainty analysis, respectively. The results for 37 countries were compared with other PAH emission inventories. It was estimated that the total global atmospheric emission of these 16 PAHs in 2004 was 520 giga grams per year (Gg y -1) with biofuel (56.7%), wildfire (17.0%) and consumer product usage (6.9%) as the major sources, and China (114 Gg y -1), India (90 Gg y -1) and United States (32 Gg y -1) were the top three countries with the highest PAH emissions. The PAH sources in the individual countries varied remarkably. For example, biofuel burning was the dominant PAH source in India, wildfire emissions were the dominant PAH source in Brazil, while consumer products were the major PAH emission source in the United States. In China, in addition to biomass combustion, coke ovens were a significant source of PAHs. Globally, benzo(a)pyrene accounted for 0.05% to 2.08% of the total PAH emission, with developing countries accounting for the higher percentages. The PAH emission density varied dramatically from 0.0013 kg km -2 y in the Falkland Islands to 360 kg km -2 y in Singapore with a global mean value of 3.98 kg km -2 y. The atmospheric emission of PAHs was positively correlated to the country's gross domestic product and negatively correlated with average income. Finally, a linear bivariate regression model was developed to explain the global PAH emission data.

  11. Iodine Determination by Microwave Plasma Torch Atomic Emission Spectrometer Coupled with Online Preconcentration Vapor Generation Technique

    Institute of Scientific and Technical Information of China (English)

    FEI Yan-qun; LUO Gui-min; FENG Guo-dong; CHEN Huan-wen; FEI Qiang; HUAN Yan-fu; JIN Qin-han

    2008-01-01

    This article focuses on iodine determination by microwave plasma torch atomic emission spectrometry (MPT-AES) coupled with online preconcentration vapor generation method.A new desolvation device,multistrand Nation dryer,was used as the substitute for condenser desolvation system.Some experimental conditions,such as preconcentration time,acidity of sample solution,rinsing solution acidity and dynamic linear range were investigated and optimized.The new desolvation system eliminates the problem of decreasing emission intensity of I(I) 206.238 nm line with the increase of working time on a conventional condenser desolvation system,thus greatly improving the reproducibility.

  12. Characteristics of polycyclic aromatic hydrocarbon emissions of particles of various sizes from smoldering incense.

    Science.gov (United States)

    Yang, T T; Lin, T S; Wu, J J; Jhuang, F J

    2012-02-01

    Release of polycyclic aromatic hydrocarbons (PAHs) in particles of various sizes from smoldering incenses was determined. Among the three types of incense investigated, yielding the total PAH emission rate and factor ranges for PM0.25 were 2,139.7-6,595.6 ng/h and 1,762.2-8,094.9 ng/g, respectively. The PM0.25/PM2.5 ratio of total PAH emission factors and rates from smoldering three incenses was greater than 0.92. This study shows that total particle PAH emission rates and factors were mainly incenses. The benzo[a]pyrene accounted for 65.2%-68.0% of the total toxic equivalency emission factor of PM2.5 for the three incenses. Experimental results clearly indicate that the PAH emission rates and factors were influenced significantly by incense composition, including carbon and hydrogen content. The study concludes that smoldering incense with low atomic hydrogen/carbon ratios minimized the production of total polycyclic aromatic hydrocarbons of both PM2.5 and PM0.25.

  13. Refueling emissions from cars in Japan: Compositions, temperature dependence and effect of vapor liquefied collection system

    Science.gov (United States)

    Yamada, Hiroyuki; Inomata, Satoshi; Tanimoto, Hiroshi

    2015-11-01

    Refueling emissions from cars available on the Japanese market, which were not equipped with specific controlling devices, were investigated. For the composition analysis, a proton transfer reaction plus switchable reagent ion mass spectrometry (PTR + SRI-MS), which is capable of real-time measurement, was used. In addition, the performance of a vapor liquefied collection system (VLCS), which is a recently developed controlling device, was evaluated and compared with an onboard refueling vapor recovery (ORVR) system. The refueling emission factor of uncontrolled vehicles at 20 °C was 1.02 ± 0.40 g/L in the case dispensing 20 L of fuel. The results of composition analysis indicated that the maximum incremental reactivity (MIR) of refueling emissions in Japan was 3.49 ± 0.83. The emissions consist of 80% alkanes and 20% alkenes, and aromatics and di-enes were negligible. C4 alkene had the highest impact on the MIR of refueling emissions. The amounts of refueling emissions were well reproduced by a function developed by MOVE2010 in the temperature range of 5-35 °C. The compositions of the refueling emissions varied in this temperature range, but the change in MIR was negligible. The trapping efficiency of VLCS was the same level as that of the ORVR (over 95%). The MIRs of refueling and evaporative emissions were strongly affected by that of the test fuel. This study and our previous study indicated that MIRbreakthrough ≈ MIRrefueling ≈ MIRfuel + 0.5 and MIRpermeation ≈ MIRfuel. The real-world estimated average MIRfuel in Japan was about 3.0.

  14. Predicting the vapor-liquid equilibrium of hydrocarbon binary mixtures and polymer solutions using predetermined pure component parameters

    Energy Technology Data Exchange (ETDEWEB)

    Ryu, Sang Kyu [Division of Chemical Engineering and Molecular Thermodynamics Laboratory, Hanyang University, Seoul 133-791 (Korea, Republic of); Bae, Young Chan, E-mail: ycbae@hanyang.ac.kr [Division of Chemical Engineering and Molecular Thermodynamics Laboratory, Hanyang University, Seoul 133-791 (Korea, Republic of)

    2012-05-25

    Highlights: Black-Right-Pointing-Pointer We have developed a close-packed lattice model for chain-like molecules. Black-Right-Pointing-Pointer The chain length dependence determined from Monte-Carlo simulation results were used. Black-Right-Pointing-Pointer To consider the volume effect, hole theory and two mixing steps were used. Black-Right-Pointing-Pointer A lattice fluid equation of state (LF-EoS) is presented for VLE of hydrocarbon mixtures. Black-Right-Pointing-Pointer Correlation of pure polymer solutions data with use of the LF-EoS. - Abstract: In our previous work, a new close-packed lattice model was developed for multi-component system of chain fluids with taking the chain length dependence from Monte-Carlo (MC) simulation results into account. In this work, we further extend this model to describe pressure, volume and temperature (PVT) properties, such as vapor-liquid equilibrium (VLE). To consider the effect of pressure on the phase behavior, the volume change effect is taken into account by introducing holes into the incompressible lattice model with two mixing steps. The corresponding new lattice fluid equation of state (LF-EoS) is applied to predict the thermodynamic properties of pure and binary mixtures of hydrocarbons as well as pure polymer solutions. The results of the proposed model are compared to other predictive approaches based on VLE calculations using predetermined pure model parameters without further adjustment. Thermodynamic properties predicted using the method developed in this work are consistent with the experimental data.

  15. Sensitivity of ozone predictions to biogenic hydrocarbon chemistry and emissions in air quality models

    Energy Technology Data Exchange (ETDEWEB)

    Jang, C.J.; Lo, S.C.Y.; Vukovich, J.; Kasibhatla, P. [MCNC-North Carolina Supercomputing Center, Research Triangle Park, NC (United States)

    1997-12-31

    Over the last decade, there is growing evidence that biogenic hydrocarbons play an important role in regional and urban ozone (O{sub 3}) formation in the United States. As a result, the regulatory guidelines issued by the USEPA require that biogenic emissions be included in photochemical modeling. Significant changes and improvement have also been made for estimating the emissions and chemical reaction rates of biogenic hydrocarbons in air quality models. In this paper the authors examine the sensitivity of ozone predictions to the changes in biogenic hydrocarbon chemistry and emissions and investigate why ozone is sensitive to these changes. They first use a Lagrangian box model, the OZIPR/EKMA model, to examine the differences of O{sub 3} predicted using two sets of chemical mechanisms, the original CB4 mechanism and the updated CB4 mechanism with new isoprene chemistry under various emission scenarios. The results show that in the selected urban case, the updated CB4 mechanism predicted lower O{sub 3} than the original CB4 mechanism because of the lower isoprene incremental reactivity in the updated CB4 mechanism. However, in the selected rural case, the updated CB4 mechanism predicted higher O{sub 3} than the original CB4, which is in contradiction to a recent OTAG study using the updated CB4 mechanism. The Eulerian grid model simulation using the MCNC`s EDSS/MAQSIP system further lends support to the box model results. The grid model simulations show that the updated CB4 mechanism predicts much lower O{sub 3} than the original CB4 mechanism over the areas where significant amount of NO{sub x} is emitted; on the contrary, over the Southeastern US region with high isoprene emission rates, the updated CB4 mechanism predicts much higher O{sub 3}.

  16. Process and apparatus for conversion of water vapor with coal or hydrocarbon into a product gas

    Energy Technology Data Exchange (ETDEWEB)

    Weirich, W.; Barnert, H.; Oertel, M.; Schulten, R.

    1990-03-27

    A process and apparatus are provided for conversion of steam and hydrocarbon, or steam and coal, into a product gas which contains hydrogen. The conversion rate is augmented by effective extraction and removal of hydrogen as and when hydrogen is generated. Within a reaction vessel wherein the conversion takes place, a chamber for collection of hydrogen is formed by the provision of a hydrogen permeable membrane. The chamber is provided with a hydrogen extraction means and houses a support structure, for example, in the form of a mesh providing structural support to the membrane. The membrane may be of a pleated or corrugated construction, so as to provide an enlarged surface for the membrane to facilitate hydrogen extraction. Also, to further facilitate hydrogen extraction, a hydrogen partial pressure differential is maintained across the membrane, such as, for example, by the counter pressure of an inert gas. A preferred configuration for the apparatus of the invention is a tubular construction which houses generally tubular hydrogen extraction chambers. 5 figs.

  17. Time trend of polycyclic aromatic hydrocarbon emission factors from motor vehicles

    Science.gov (United States)

    Tao, Shu; Shen, Huizhong; Wang, Rong; Sun, Kang

    2010-05-01

    Motor vehicle is an important emission source of polycyclic aromatic hydrocarbons (PAHs) and this is particularly true in urban areas. Motor vehicle emission factors (EFs) for individual PAH compound reported in the literature varied for 4 to 5 orders of magnitude, leading to high uncertainty in emission estimation. In this study, the major factors affecting EFs were investigated and characterized by regression models. Based on the model developed, a motor vehicle PAH emission inventory at country level was developed. It was found that country and model year are the most important factors affecting EFs for PAHs. The influence of the two factors can be quantified by a single parameter of per capita gross domestic production (purchasing power parity), which was used as the independent variables of the regression models. The models developed using randomly selected 80% of measurements and tested with the remained data accounted for 28 to 48% of the variations in EFs for PAHs measured in 16 countries over 50 years. The regression coefficients of the EF prediction models were molecular weight dependent. Motor vehicle emission of PAHs from individual countries in the world in 1985, 1995, 2005, 2015, and 2025 were calculated and the global emission of total PAHs were 470, 390, and 430 Gg in 1985, 1995, and 2005 and will be 290 and 130 Gg in 2015 and 2025, respectively. The emission is currently passing its peak and will decrease due to significant decrease in China and other developing countries.

  18. Emission of Polycyclic Aromatic Hydrocarbons from the Exhalation Zones of Thermally Active Mine Waste Dumps

    Directory of Open Access Journals (Sweden)

    Patrycja Kuna-Gwoździewicz

    2013-01-01

    Full Text Available The article presents results of research carried out on the occurrence of polycyclic aromatic hydrocarbons (PAH in gases of exhalation zones, created on the surface of a thermally active coal mine waste dump. The oxidation and self-heating of mine waste are accompanied with the intensive emission of flue gases, including PAH group compounds. Taking into consideration the fact the hydrocarbons show strong genotoxic, mutagenic and carcinogenic properties, research was conducted to establish their content in the examined gases. The research object was a gangue dump located in Rybnik. The research was performed in 2012. In total, 24 samples of gas were collected with PUF (polyurethane foam sampling cartridges with a quartz fibre filter and an aspirator. The collected samples were analysed with the use of high performance liquid chromatography (HPLC and a fluorescence detector (FLD to evaluate the amount of PAH present.

  19. Toroidally Asymmetric Distributions of Hydrocarbon (CD) Emission and Chemical Sputtering Sources in DIII-D

    Energy Technology Data Exchange (ETDEWEB)

    Groth, M; Brooks, N H; Fenstermacher, M E; Lasnier, C J; McLean, A G; Watkins, J G

    2006-05-16

    Measurements in DIII-D show that the carbon chemical sputtering sources along the inner divertor and center post are toroidally periodic and highest at the upstream tile edge. Imaging with a tangentially viewing camera and visible spectroscopy were used to monitor the emission from molecular hydrocarbons (CH/CD) at 430.8 nm and deuterium neutrals in attached and partially detached divertors of low-confinement mode plasmas. In contrast to the toroidally periodic CD distribution, emission from deuterium neutrals was observed to be toroidally symmetric along the inner strike zone. The toroidal distribution of the measured tile surface temperature in the inner divertor correlates with that of the CD emission, suggesting larger parallel particle and heat fluxes to the upstream tile edge, either due to toroidal tile gaps or height steps between adjacent tiles.

  20. Emissions of polycyclic aromatic hydrocarbons, polychlorinated dibenzo-p-dioxins, and dibenzofurans from incineration of nanomaterials.

    Science.gov (United States)

    Vejerano, Eric P; Holder, Amara L; Marr, Linsey C

    2013-05-07

    Disposal of some nanomaterial-laden waste through incineration is inevitable, and nanomaterials' influence on combustion byproduct formation under high-temperature, oxidative conditions is not well understood. This work reports the formation of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated-dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) from incineration of paper and plastic waste containing various nanomaterials, including titania, nickel oxide, silver, ceria, iron oxide, quantum dots, and C60-fullerene, in a laboratory-scale furnace. The presence of nanomaterials in the waste stream resulted in higher emissions of some PAH species and lower emissions of others, depending on the type of waste. The major PAH species formed were phenanthrene and anthracene, and emissions were sensitive to the amount of nanomaterials in the waste. Generally, there were no significant differences in emission factors for the larger PAH species when nanomaterials were added to the waste. The total PAH emission factors were on average ~6 times higher for waste spiked with nanomaterials v. their bulk counterparts. Emissions of chlorinated dioxins from poly(vinyl chloride) (PVC) waste were not detected; however, chlorinated furans were formed at elevated concentrations with wastes containing silver and titania nanomaterials, and toxicity was attributable mainly to 2,3,4,7,8-pentachlorodibenzofuran. The combination of high specific surface area and catalytic, including electrocatalytic, properties of nanomaterials might be responsible for affecting the formation of toxic pollutants during incineration.

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

    Science.gov (United States)

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

    2006-03-01

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

  2. The emissions of monoaromatic hydrocarbons from small polymeric toys placed in chocolate food products.

    Science.gov (United States)

    Marć, Mariusz; Formela, Krzysztof; Klein, Marek; Namieśnik, Jacek; Zabiegała, Bożena

    2015-10-15

    The article presents findings on the emissions of selected monoaromatic hydrocarbons from children's toys placed in chocolate food products. The emission test system involved the application of a new type of microscale stationary emission chamber, μ-CTE™ 250. In order to determine the type of the applied polymer in the manufacture of the tested toys, Fourier transform infrared spectroscopy and thermogravimetric analysis coupled with differential scanning calorimetry were used. It was found that the tested toy components or the whole toys (figurines) are made of two main types of polymers: polyamide and acrylonitrile-butadiene-styrene copolymer. Total number of studied small polymeric toys was 52. The average emissions of selected monoaromatic hydrocarbons from studied toys made of polyamide were as follows: benzene: 0.45 ± 0.33 ng/g; toluene: 3.3 ± 2.6 ng/g; ethylbenzene: 1.4 ± 1.4 ng/g; p,m-xylene: 2.5 ± 4.5 ng/g; and styrene: 8.2 ± 9.9 ng/g. In the case of studied toys made of acrylonitrile-butadiene-styrene copolymer the average emissions of benzene, toluene, ethylbeznene, p,m-xylene and styrene were: 0.31 ± 0.29 ng/g; 2.5 ± 1.4 ng/g; 4.6 ± 8.9 ng/g; 1.4 ± 1.1 ng/g; and 36 ± 44 ng/g, respectively.

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

    Science.gov (United States)

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

    2017-01-01

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

  4. Vapor emissions resulting from Nd:YAG laser interaction with tooth structure.

    Science.gov (United States)

    Gelskey, S C; White, J M; Gelskey, D E; Kremers, W

    1998-11-01

    The Neodymium:yttrium aluminum garnet (Nd:YAG) dental laser has been cleared by the United States Food and Drug Administration (FDA) for marketing in intraoral soft tissue treatment. The efficacy and safety of the Nd:YAG laser in the treatment of hard dental tissue as well as the effects of dental irradiation on the pulp and periodontium have been investigated. Odors resulting from laser irradiation have been reported, but the nature and toxicity of associated decomposition vapors is unknown and the health consequences of their inhalation have not yet been studied. The purpose of this in vitro study was to identify vapors emitted during interaction of the Nd:YAG laser with carious human enamel and dentin and sound enamel and dentin coated with organic ink. Vapor emissions were collected from prepared sections of extracted human teeth receiving laser irradiation of 100 mJ and 10 Hz for a duration of 1, 10, or 60 s. Emissions were collected by means of charcoal absorption tubes, and subsequently analyzed using a Gas Chromatograph equipped with Mass Selective (GC/MS) and Flame Ionization Detectors to identify the chemical constituents of the vapors. No compounds were identified in Nd:YAG laser-treated caries, enamel and dentin. No volatile vapors were identified from samples of tooth materials exposed to the laser for 1 or 10 s. Camphor was positively identified in the test sample which consisted of India ink-coated dentin and the reference sample of India ink-coated glass beads, both exposed to the laser for 60 s. 2,5-norbornadiene was tentatively identified in these samples. The Threshold Limit Value (TLV) of camphor is 2 ppm with a Lethal Dose Level (LDLo) of 50 mg/kg (human oral), while the TLV and LDLo of 2,5-norbornadiene is unknown. Occupational and public health safety measures are discussed in this article. Further research is needed to quantify the compounds produced and to determine their toxicity to patients and to dental care providers.

  5. Directional infrared emission resulting from cascade population inversion and four-wave mixing in Rb vapor.

    Science.gov (United States)

    Akulshin, Alexander; Budker, Dmitry; McLean, Russell

    2014-02-15

    Directional infrared emission at 1.37 and 5.23 μm is generated in Rb vapors that are stepwise excited by low-power cw resonant light. The radiation at 5.23 μm originating from amplified spontaneous emission on the 5D(5/2)→6P(3/2) transition and wave mixing consists of forward- and backward-directed components with distinctive spectral and spatial properties. Diffraction-limited light at 1.37 μm generated in the copropagating direction only is a product of parametric wave mixing around the 5P(3/2)→5D(5/2)→6P(3/2)→6S(1/2)→5P(3/2) transition loop. This highly nondegenerate mixing process involves one externally applied and two internally generated optical fields. Similarities between wave mixing generated blue and 1.37 μm light are demonstrated.

  6. A Techno-Economic Analysis of Emission Controls on Hydrocarbon Biofuel Production

    Energy Technology Data Exchange (ETDEWEB)

    Bhatt, Arpit; Zhang, Yimin; Davis, Ryan; Eberle, Annika; Heath, Garvin

    2016-06-23

    Biofuels have the potential to reduce our dependency on petroleum-derived transportation fuels and decrease greenhouse gas (GHG) emissions. Although the overall GHG emissions from biofuels are expected to be lower when compared to those of petroleum fuels, the process of converting biomass feedstocks into biofuels emits various air pollutants, which may be subject to federal air quality regulation or emission limits. While prior research has evaluated the technical and economic feasibility of biofuel technologies, gaps still exist in understanding the regulatory issues associated with the biorefineries and their economic implications on biofuel production costs (referred to as minimum fuel selling price (MFSP) in this study). The aim of our research is to evaluate the economic impact of implementing emission reduction technologies at biorefineries and estimate the cost effectiveness of two primary control technologies that may be required for air permitting purposes. We analyze a lignocellulosic sugars-to-hydrocarbon biofuel production pathway developed by the National Renewable Energy Laboratory (NREL) and implement air emission controls in Aspen Plus to evaluate how they affect the MFSP. Results from this analysis can help inform decisions about biorefinery siting and sizing, as well as mitigate the risks associated with air permitting.

  7. Emission-dominated gas exchange of elemental mercury vapor over natural surfaces in China

    Science.gov (United States)

    Wang, Xun; Lin, Che-Jen; Yuan, Wei; Sommar, Jonas; Zhu, Wei; Feng, Xinbin

    2016-09-01

    Mercury (Hg) emission from natural surfaces plays an important role in global Hg cycling. The present estimate of global natural emission has large uncertainty and remains unverified against field data, particularly for terrestrial surfaces. In this study, a mechanistic model is developed for estimating the emission of elemental mercury vapor (Hg0) from natural surfaces in China. The development implements recent advancements in the understanding of air-soil and air-foliage exchange of Hg0 and redox chemistry in soil and on surfaces, incorporates the effects of soil characteristics and land use changes by agricultural activities, and is examined through a systematic set of sensitivity simulations. Using the model, the net exchange of Hg0 between the atmosphere and natural surfaces of mainland China is estimated to be 465.1 Mg yr-1, including 565.5 Mg yr-1 from soil surfaces, 9.0 Mg yr-1 from water bodies, and -100.4 Mg yr-1 from vegetation. The air-surface exchange is strongly dependent on the land use and meteorology, with 9 % of net emission from forest ecosystems; 50 % from shrubland, savanna, and grassland; 33 % from cropland; and 8 % from other land uses. Given the large agricultural land area in China, farming activities play an important role on the air-surface exchange over farmland. Particularly, rice field shift from a net sink (3.3 Mg uptake) during April-October (rice planting) to a net source when the farmland is not flooded (November-March). Summing up the emission from each land use, more than half of the total emission occurs in summer (51 %), followed by spring (28 %), autumn (13 %), and winter (8 %). Model verification is accomplished using observational data of air-soil/air-water fluxes and Hg deposition through litterfall for forest ecosystems in China and Monte Carlo simulations. In contrast to the earlier estimate by Shetty et al. (2008) that reported large emission from vegetative surfaces using an evapotranspiration approach, the estimate in

  8. Size-resolved polycyclic aromatic hydrocarbon emission factors from on-road gasoline and diesel vehicles: temperature effect on the nuclei-mode.

    Science.gov (United States)

    Eiguren-Fernandez, Arantzazu; Miguel, Antonio H

    2012-03-06

    Motor vehicles are a major source of polycyclic aromatic hydrocarbon (PAH) emissions in urban areas. Motor vehicle emission control strategies have included improvements in engine design, exhaust emission control, and fuel reformulation. Therefore, an updated assessment of the effects of the shifts in fuels and vehicle technologies on PAH vehicular emission factors (EFs) is needed. We have evaluated the effects of ambient temperature on the size-resolved EFs of nine US EPA Priority Pollutant PAH, down to 10 nm diameter, from on-road California gasoline light-duty vehicles with spark ignition (SI) and heavy-duty diesels with compression ignition (CI) in summer 2004 and winter 2005. During the winter, for the target PAH with the lowest subcooled equilibrium vapor pressure --benzo[a]pyrene, benzo[ghi]perylene, and indeno[1,2,3-cd]pyrene-- the mass in the nucleation mode, defined here as particles with dp <32 nm, ranged between 14 and 38% for SI vehicles and 29 and 64% for CI vehicles. Our observations of the effect of temperature on the mass of PAH in the nucleation mode are similar to the observed effect of temperature on the number concentration of diesel exhaust particles in the nucleation mode in a previous report.

  9. Polycyclic aromatic hydrocarbon and mid-infrared continuum emission in a z > 4 submillimeter galaxy

    Energy Technology Data Exchange (ETDEWEB)

    Riechers, Dominik A. [Department of Astronomy, Cornell University, 220 Space Sciences Building, Ithaca, NY 14853 (United States); Pope, Alexandra [Department of Astronomy, University of Massachusetts, Amherst, MA 01003 (United States); Daddi, Emanuele; Elbaz, David [Laboratoire AIM, CEA/DSM-CNRS-Université Paris Diderot, Irfu/Service d' Astrophysique, CEA Saclay, Orme des Merisiers, F-91191 Gif-sur-Yvette Cedex (France); Armus, Lee; Chary, Ranga-Ram [Spitzer Science Center, California Institute of Technology, MC 220-6, 1200 East California Boulevard, Pasadena, CA 91125 (United States); Carilli, Christopher L. [National Radio Astronomy Observatory, PO Box O, Socorro, NM 87801 (United States); Walter, Fabian; Hodge, Jacqueline [Max-Planck-Institut für Astronomie, Königstuhl 17, D-69117 Heidelberg (Germany); Morrison, Glenn E. [Canada-France-Hawaii Telescope, 65-1238 Mamalahoa Hwy, Kamuela, HI 96743-8432 (United States); Dickinson, Mark [National Optical Astronomy Observatory, 950 North Cherry Avenue, Tucson, AZ 85719 (United States); Dannerbauer, Helmut, E-mail: dr@astro.cornell.edu [Institut für Astrophysik, Universität Wien, Türkenschanzstraße 17, A-1180 Wien (Austria)

    2014-05-01

    We report the detection of 6.2 μm polycyclic aromatic hydrocarbon (PAH) and rest-frame 4-7 μm continuum emission in the z = 4.055 submillimeter galaxy GN20, using the Infrared Spectrograph on board the Spitzer Space Telescope. This represents the first detection of PAH emission at z > 4. The strength of the PAH emission feature is consistent with a very high star formation rate of ∼1600 M {sub ☉} yr{sup –1}. We find that this intense starburst powers at least ∼1/3 of the faint underlying 6 μm continuum emission, with an additional, significant (and perhaps dominant) contribution due to a power-law-like hot dust source, which we interpret to likely be a faint, dust-obscured active galactic nucleus (AGN). The inferred 6 μm AGN continuum luminosity is consistent with a sensitive upper limit on the hard X-ray emission as measured by the Chandra X-Ray Observatory if the previously undetected AGN is Compton-thick. This is in agreement with the finding at optical/infrared wavelengths that the galaxy and its nucleus are heavily dust-obscured. Despite the strong power-law component enhancing the mid-infrared continuum emission, the intense starburst associated with the photon-dominated regions that give rise to the PAH emission appears to dominate the total energy output in the infrared. GN20 is one of the most luminous starburst galaxies known at any redshift, embedded in a rich protocluster of star-forming galaxies. This investigation provides an improved understanding of the energy sources that power such exceptional systems, which represent the extreme end of massive galaxy formation at early cosmic times.

  10. Far-Infrared Spectroscopy of Cationic Polycyclic Aromatic Hydrocarbons: Zero Kinetic Energy Photoelectron Spectroscopy of Pentacene Vaporized from Laser Desorption

    CERN Document Server

    Zhang, J; Pei, L; Kong, W; Li, Aigen

    2012-01-01

    The distinctive set of infrared (IR) emission bands at 3.3, 6.2, 7.7, 8.6, and 11.3{\\mu}m are ubiquitously seen in a wide variety of astrophysical environments. They are generally attributed to polycyclic aromatic hydrocarbon (PAH) molecules. However, not a single PAH species has yet been identified in space, as the mid-IR vibrational bands are mostly representative of functional groups and thus do not allow one to fingerprint individual PAH molecules. In contrast, the far-IR (FIR) bands are sensitive to the skeletal characteristics of a molecule, hence they are important for chemical identification of unknown species. With an aim to offer laboratory astrophysical data for the Herschel Space Observatory, Stratospheric Observatory for Infrared Astronomy, and similar future space missions, in this work we report neutral and cation FIR spectroscopy of pentacene (C_22H_14), a five-ring PAH molecule. We report three IR active modes of cationic pentacene at 53.3, 84.8, and 266{\\mu}m that may be detectable by space ...

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

    Science.gov (United States)

    Shen, Huizhong; Tao, Shu

    2014-05-01

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

  12. Random mixtures of polycyclic aromatic hydrocarbon spectra match interstellar infrared emission

    CERN Document Server

    Rosenberg, Marissa J F; Boersma, Christiaan

    2014-01-01

    The mid-infrared (IR; 5-15~$\\mu$m) spectrum of a wide variety of astronomical objects exhibits a set of broad emission features at 6.2, 7.7, 8.6, 11.3 and 12.7 $\\mu$m. About 30 years ago it was proposed that these signatures are due to emission from a family of UV heated nanometer-sized carbonaceous molecules known as polycyclic aromatic hydrocarbons (PAHs), causing them to be referred to as aromatic IR bands (AIBs). Today, the acceptance of the PAH model is far from settled, as the identification of a single PAH in space has not yet been successful and physically relevant theoretical models involving ``true'' PAH cross sections do not reproduce the AIBs in detail. In this paper, we use the NASA Ames PAH IR Spectroscopic Database, which contains over 500 quantum-computed spectra, in conjunction with a simple emission model, to show that the spectrum produced by any random mixture of at least 30 PAHs converges to the same 'kernel'-spectrum. This kernel-spectrum captures the essence of the PAH emission spectrum...

  13. Emission factors of polycyclic aromatic hydrocarbons from domestic coal combustion in China.

    Science.gov (United States)

    Geng, Chunmei; Chen, Jianhua; Yang, Xiaoyang; Ren, Lihong; Yin, Baohui; Liu, Xiaoyu; Bai, Zhipeng

    2014-01-01

    Domestic coal stove is widely used in China, especially for countryside during heating period of winter, and polycyclic aromatic hydrocarbons (PAHs) are important in flue gas of the stove. By using dilution tunnel system, samples of both gaseous and particulate phases from domestic coal combustion were collected and 18 PAH species were analyzed by GC-MS. The average emission factors of total 18 PAH species was 171.73 mg/kg, ranging from 140.75 to 229.11 mg/kg for bituminous coals, while was 93.98 mg/kg, ranging from 58.48 to 129.47 mg/kg for anthracite coals. PAHs in gaseous phases occupied 95% of the total of PAHs emission of coal combustion. In particulate phase, 3-ring and 4-ring PAHs were the main components, accounting for 80% of the total particulate PAHs. The total toxicity potency evaluated by benzo[a]pyrene-equivalent carcinogenic power, sum of 7 carcinogenic PAH components and 2,3,7,8-tetrachlorodibenzodioxin had a similar tendency. And as a result, the toxic potential of bituminous coal was higher than that of anthracite coal. Efficient emission control should be conducted to reduce PAH emissions in order to protect ecosystem and human health.

  14. [Emission factors of polycyclic aromatic hydrocarbons (PAHs) in residential coal combustion and its influence factors].

    Science.gov (United States)

    Hai, Ting-Ting; Chen, Ying-Jun; Wang, Yan; Tian, Chong-Guo; Lin, Tian

    2013-07-01

    As the emission source of polycyclic aromatic hydrocarbons (PAHs), domestic coal combustion has attracted increasing attention in China. According to the coal maturity, combustion form and stove type associated with domestic coal combustion, a large-size, full-flow dilution tunnel and fractional sampling system was employed to collect the emissions from five coals with various maturities, which were burned in the form of raw-coal-chunk (RCC)/honeycomb-coal-briquettes (HCB) in different residential stoves, and then the emission factors of PAHs (EF(PAHs)) were achieved. The results indicate that the EF(PAHs) of bituminous coal ranged from 1.1 mg x kg(-1) to 3.9 mg x kg(-1) for RCC and 2.5 mg x kg(-1) to 21. 1 mg x kg(-1) for HCB, and the anthracite EF(PAH8) were 0.2 mg x kg(-1) for RCC and 0.6 mg x kg(-1) for HCB, respectively. Among all the influence factors of emission factors of PAHs from domestic coal combustion, the maturity of coal played a major role, the range of variance reaching 1 to 2 orders of magnitude in coals with different maturity. Followed by the form of combustion (RCC/HCB), the EF(PAHs) of HCB was 2-6 times higher than that of RCC for the same geological maturity of the coal. The type of stove had little influence on EF(PAHs).

  15. Emission and Size Distribution of Particle-bound Polycyclic Aromatic Hydrocarbons from Residential Wood Combustion

    Science.gov (United States)

    Shen, Guofeng; Wei, Siye; Zhang, Yanyan; Wang, Bin; Wang, Rong; Shen, Huizhong; Li, Wei; Huang, Ye; Chen, Yuanchen; Chen, Han; Tao, Shu

    2015-01-01

    Emissions and size distributions of 28 particle-bound polycyclic aromatic hydrocarbons (PAHs) from residential combustion of 19 fuels in a domestic cooking stove in rural China were studied. Measured emission factors of total PAHs were 1.79±1.55, 12.1±9.1, and 5.36±4.46 mg/kg for fuel wood, brushwood, and bamboo, respectively. Approximate 86.7, 65.0, and 79.7% of the PAHs were associated with fine particulate matter with size less than 2.1 µm for these three types of fuels. Statistically significant difference in emission factors and size distributions of particle-bound PAHs between fuel wood and brushwood was observed, with the former had lower emission factors but more PAHs in finer PM. Mass fraction of the fine particles associated PAHs was found to be positively correlated with fuel density and moisture, and negatively correlated with combustion efficiency. Low and high molecular weight PAHs segregated into the coarse and fine PM, respectively. The high accumulation tendency of the PAHs from residential wood combustion in fine particles implies strong adverse health impact. PMID:25678760

  16. Greenhouse gas impacts of declining hydrocarbon resource quality: Depletion, dynamics, and process emissions

    Science.gov (United States)

    Brandt, Adam Robert

    This dissertation explores the environmental and economic impacts of the transition to hydrocarbon substitutes for conventional petroleum (SCPs). First, mathematical models of oil depletion are reviewed, including the Hubbert model, curve-fitting methods, simulation models, and economic models. The benefits and drawbacks of each method are outlined. I discuss the predictive value of the models and our ability to determine if one model type works best. I argue that forecasting oil depletion without also including substitution with SCPs results in unrealistic projections of future energy supply. I next use information theoretic techniques to test the Hubbert model of oil depletion against five other asymmetric and symmetric curve-fitting models using data from 139 oil producing regions. I also test the assumptions that production curves are symmetric and that production is more bell-shaped in larger regions. Results show that if symmetry is enforced, Gaussian production curves perform best, while if asymmetry is allowed, asymmetric exponential models prove most useful. I also find strong evidence for asymmetry: production declines are consistently less steep than inclines. In order to understand the impacts of oil depletion on GHG emissions, I developed the Regional Optimization Model for Emissions from Oil Substitutes (ROMEO). ROMEO is an economic optimization model of investment and production of fuels. Results indicate that incremental emissions (with demand held constant) from SCPs could be 5-20 GtC over the next 50 years. These results are sensitive to the endowment of conventional oil and not sensitive to a carbon tax. If demand can vary, total emissions could decline under a transition because the higher cost of SCPs lessens overall fuel consumption. Lastly, I study the energetic and environmental characteristics of the in situ conversion process, which utilizes electricity to generate liquid hydrocarbons from oil shale. I model the energy inputs and outputs

  17. Trends of non-methane hydrocarbons (NMHC emissions in Beijing during 2002–2013

    Directory of Open Access Journals (Sweden)

    M. Wang

    2014-07-01

    Full Text Available Non-methane hydrocarbons (NMHCs play a critical role in the photochemical production of ozone (O3 and organic aerosols. Obtaining an accurate understanding on NMHC emission trends is essential for predicting air quality changes and evaluating the effectiveness of current control measures. In this study, we evaluated temporal trends in NMHC emissions in Beijing based on ambient measurements during the summer at an urban site in Beijing from 2002 to 2013. In contrast to the results of the most recent inventory (Multi-resolution Emission Inventory for China, MEIC, which reported that total NMHC emissions increased at a rate of ~4% yr−1, mixing ratios of NMHCs measured at this urban site displayed an obvious decrease (~30% during the last decade. A Positive Matrix Factorization (PMF model was applied to the NMHC measurements for source apportionment, and the results showed a decrease in the concentrations contributed by transportation-related sources to total NMHC emissions by 66% during 2004–2012, which was comparable to the relative decline of 65% reported by the MEIC inventory. This finding indicates that the implementation of stricter emissions standards and control measures has been effective for reducing transportation-related NMHC emissions. In addition, the PMF results suggested that there were no significant temporal changes in NMHC concentrations from paint and solvent use during 2004–2012, in contrast with the rapid rate of increase (27.5% yr−1 reported by the MEIC inventory. To re-evaluate the NMHC emissions trends for paint and solvent use, annual variations in NMHC / NOx ratios were compared between ambient measurements and the MEIC inventory. In contrast to the significant rise in NMHC / NOx ratios from the inventory, the measured ratios declined by 14% during 2005–2012. However, the inferred NMHC / NOx ratios based on PMF results exhibited a comparable decline of 11% to measurements. These results indicate that the increase

  18. Characterization and concentrations of polycyclic aromatic hydrocarbons in emissions from different heating systems in Damascus, Syria.

    Science.gov (United States)

    Alkurdi, Farouk; Karabet, François; Dimashki, Marwan

    2014-04-01

    Traffic has long been recognized as the major contributor to polycyclic aromatic hydrocarbon (PAH) emissions to the urban atmosphere. Stationary combustion sources, including residential space heating systems, are also a major contributor to PAH emissions. The aim of this study was to determine the profile and concentration of PAHs in stack flue gas emissions from different kinds of space heaters in order to increase the understanding of the scale of the PAH pollution problem caused by this source. This study set out to first assess the characteristics of PAHs and their corresponding benzo[a]pyrene equivalent emissions from a few types of domestic heaters and central heating systems to the urban atmosphere. The study, enabled for the first time, the characterization of PAHs in stationary combustion sources in the city of Damascus, Syria. Nine different types of heating systems were selected with respect to age, design, and type of fuel burned. The concentrations of 15 individual PAH compounds in the stack flue gas were determined in the extracts of the collected samples using high-performance liquid chromatography system (HPLC) equipped with ultraviolet-visible and fluorescence detectors. In general, older domestic wood stoves caused considerably higher PAH emissions than modern domestic heaters burning diesel oil. The average concentration of ΣPAH (sum of 15 compounds) in emissions from all types of studied heating systems ranged between 43 ± 0.4 and 316 ± 1.4 μg/m(3). Values of total benzo[a]pyrene equivalent ranged between 0.61 and 15.41 μg/m(3).

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

    Science.gov (United States)

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

    2012-06-01

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

  20. Near surface soil vapor clusters for monitoring emissions of volatile organic compounds from soils.

    Science.gov (United States)

    Ergas, S J; Hinlein, E S; Reyes, P O; Ostendorf, D W; Tehrany, J P

    2000-01-01

    The overall objective of this research was to develop and test a method of determining emission rates of volatile organic compounds (VOCs) and other gases from soil surfaces. Soil vapor clusters (SVCs) were designed as a low dead volume, robust sampling system to obtain vertically resolved profiles of soil gas contaminant concentrations in the near surface zone. The concentration profiles, when combined with a mathematical model of porous media mass transport, were used to calculate the contaminant flux from the soil surface. Initial experiments were conducted using a mesoscale soil remediation system under a range of experimental conditions. Helium was used as a tracer and trichloroethene was used as a model VOC. Flux estimations using the SVCs were within 25% of independent surface flux estimates and were comparable to measurements made using a surface isolation flux chamber (SIFC). In addition, method detection limits for the SVC were an order of magnitude lower than detection limits with the SIFC. Field trials, conducted with the SVCs at a bioventing site, indicated that the SVC method could be easily used in the field to estimate fugitive VOC emission rates. Major advantages of the SVC method were its low detection limits, lack of required auxiliary equipment, and ability to obtain real-time estimates of fugitive VOC emission rates.

  1. Indoor emission, dispersion and exposure of total particle-bound polycyclic aromatic hydrocarbons during cooking

    Science.gov (United States)

    Gao, Jun; Jian, Yating; Cao, Changsheng; Chen, Lei; Zhang, Xu

    2015-11-01

    Cooking processes highly contribute to indoor polycyclic aromatic hydrocarbon (PAH) pollution. High molecular weight and potentially carcinogenic PAHs are generally found attached to small particles, i.e., particulate phase PAHs (PPAHs). Due to the fact that indoor particle dynamics have been clear, describing the indoor dynamics of cooking-generated PPAHs within a specific time span is possible. This paper attempted to quantify the dynamic emission rate, simultaneous spatial dispersion and individual exposure of PPAHs using a cooking source. Experiments were conducted in a real-scale kitchen chamber to elucidate the time-resolved emission and effect of edible oil temperature and mass. Numerical simulations based on indoor particle dynamics were performed to obtain the spatial dispersion and individual inhalation intake of PPAHs under different emission and ventilation conditions. The present work examined the preheating cooking stage, at which edible oil is heated up to beyond its smoke point. The dynamic emission rate peak point occurred much earlier than the oil heating temperature. The total PPAH emission ranged from 2258 to 6578 ng upon heating 40-85 g of edible oil. The overall intake fraction by an individual within a period of 10 min, including 3 min for heating and 7 min for natural cooling, was generally ∼1/10,000. An important outcome of this work was that the overall intake fraction could be represented by multiplying the range hood escape efficiency by the inhalation-to-ventilation rate ratio, which would be no greater than the same ratio. The methodology and results of this work were extendible for the number-based assessment of PPAHs. This work is expected to help us understand the health risks due to inhalation exposure to cooking-generated PPAHs in the kitchen.

  2. Emission of polycyclic aromatic hydrocarbons (PAHs) from the liquid injection incineration of petrochemical industrial wastewater.

    Science.gov (United States)

    Wang, Lin-Chi; Wang, I-Ching; Chang, Juu-En; Lai, Soon-Onn; Chang-Chien, Guo-Ping

    2007-09-05

    This study investigated the emission of polycyclic aromatic hydrocarbons (PAHs) from stack flue gas and air pollution control device (APCD) effluent of the liquid injection incinerator (LII) disposing the petrochemical industrial wastewater, and PAH removal efficiencies of wet electrostatic precipitator (WESP) and wet scrubber (WSB). The PAH carcinogenic potency were investigated with the benzo(a)pyrene equivalent concentration (BaP(eq)). The remarkably high total-BaP(eq) concentration (220 microgNm(-3)) in the stack flue gas was much higher than those of several published emission sources, and indicated the possible influence on its surrounding environment. The total-PAH emission factors of the WESP, WSB and stack flue gas were 78.9, 95.7 and 30,900 microgL(-1) wastewater, respectively. The removal efficiencies of total-PAHs were 0.254, 0.309 and 0.563% for WESP, WSB and overall, respectively, suggesting that the use of both WESP and WSB shows insignificant PAH removal efficiencies, and 99.4% of total-PAHs was directly emitted to the ambient air through the stack flue gas. This finding suggested that the better incineration efficiencies, and APCD removal efficiencies for disposing the petrochemical industrial wastewater are necessary in future.

  3. Emission of polycyclic aromatic hydrocarbons and lead during Chinese mid-autumn festival.

    Science.gov (United States)

    Kuo, Chung-Yih; Lee, Hong-Shen; Lai, Jeang-Hung

    2006-07-31

    The emission factors of total particulate polycyclic aromatic hydrocarbons (PAHs), Benzo(a)pyrene (BaP), BaP-equivalent doses (BaP(eq)) and Pb for burning three kinds of charcoal were investigated in this study: fast-lighting charcoal, Taiwanese, and Indonesian charcoal (the latter two of which are not fast-lighting). Compared to the burning of Taiwanese and Indonesian charcoal, the burning of fast-lighting charcoal can emit much larger amounts of total PAHs, BaP(eq) and Pb into the atmosphere. The emission factors of total PAHs, BaP and BaP(eq) for broiling meat were noticeably higher than those for broiling vegetables and non-fish seafood. When using Indonesian charcoal to broil meat, the total emission factors of particulate PAHs and BaP were about 15.7 and 0.39 mg/kg, respectively. The total amounts of particulate PAHs and Pb emitted from cookouts during Mid-Autumn Festival were 2881 and 120 g, respectively. Total PAHs and BaP(eq) in PM(10) aerosols on Mid-Autumn Festival nights increased about 1.6 and 1.5 times, respectively, higher than those on non-festival nights. The mean concentration of Pb on the nights of Mid-Autumn Festival increases to about 2.8 times that of non-festival nights.

  4. The Luminous Polycyclic Aromatic Hydrocarbon Emission Features: Applications to High Redshift Galaxies and Active Galactic Nuclei

    Science.gov (United States)

    Shipley, Heath V.

    2016-01-01

    For decades, significant work has been applied to calibrating emission from the ultra-violet, nebular emission lines, far-infrared, X-ray and radio as tracers of the star-formation rate (SFR) in distant galaxies. Understanding the exact rate of star-formation and how it evolves with time and galaxy mass has deep implications for how galaxies form. The co-evolution of star-formation and supermassive black hole (SMBH) accretion is one of the key problems in galaxy formation theory. But, many of these SFR indicators are influenced by SMBH accretion in galaxies and result in unreliable SFRs. Utilizing the luminous polycyclic aromatic hydrocarbon (PAH) emission features, I provide a new robust SFR calibration using the luminosity emitted from the PAHs at 6.2μm, 7.7μm and 11.3μm to solve this. The PAH features emit strongly in the mid-infrared (mid-IR; 5-25μm) mitigating dust extinction, containing on average 5-10% of the total IR luminosity in galaxies. I use a sample of 105 star-forming galaxies covering a range of total IR luminosity, LIR = L(8-1000μm) = 109 - 1012 L⊙ and redshift 0 blackhole accretion contemporaneously in a galaxy.

  5. Biomass consumption and CO2, CO and main hydrocarbon gas emissions in an Amazonian forest clearing fire

    Science.gov (United States)

    T. G. Soares Neto; J. A. Carvalho; C. A. G. Veras; E. C. Alvarado; R. Gielow; E. N. Lincoln; T. J. Christian; R. J. Yokelson; J. C. Santos

    2009-01-01

    Biomass consumption and CO2, CO and hydrocarbon gas emissions in an Amazonian forest clearing fire are presented and discussed. The experiment was conducted in the arc of deforestation, near the city of Alta Floresta, state of Mato Grosso, Brazil. The average carbon content of dry biomass was 48% and the estimated average moisture content of fresh biomass was 42% on...

  6. POLYCYCLIC AROMATIC HYDROCARBON EMISSION IN SPITZER/IRS MAPS. I. CATALOG AND SIMPLE DIAGNOSTICS

    Energy Technology Data Exchange (ETDEWEB)

    Stock, D. J.; Choi, W. D.-Y.; Moya, L. G. V.; Otaguro, J. N.; Sorkhou, S.; Peeters, E. [Department of Physics and Astronomy, University of Western Ontario, London, ON, N6A 3K7 (Canada); Allamandola, L. J. [NASA Ames Research Center, MS 245-6, Moffett Field, CA 94035-0001 (United States); Tielens, A. G. G. M., E-mail: dstock4@uwo.ca [Leiden Observatory, Leiden University, P.O. Box 9513, 2300 RA (Netherlands)

    2016-03-01

    We present a sample of resolved galactic H ii regions and photodissociation regions (PDRs) observed with the Spitzer infrared spectrograph in spectral mapping mode between the wavelengths of 5–15 μm. For each object we have spectral maps at a spatial resolution of ∼4″ in which we have measured all of the mid-infrared emission and absorption features. These include the polycyclic aromatic hydrocarbon (PAH) emission bands, primarily at 6.2, 7.7, 8.6, 11.2, and 12.7 μm, as well as the spectral emission lines of neon and sulfur and the absorption band caused by silicate dust at around 9.8 μm. In this work we describe the data in detail, including the data reduction and measurement strategies, and subsequently present the PAH emission band intensity correlations for each of the objects and the sample as a whole. We find that there are distinct differences between the sources in the sample, with two main groups: the first comprising the H ii regions and the second the reflection nebulae (RNe). Three sources—the reflection nebula NGC 7023, the Horsehead nebula PDR (an interface between the H ii region IC 434 and the Orion B molecular cloud), and M17—resist this categorization, with the Horsehead PDR points mimicking the RNe and the NGC 7023 fluxes displaying a unique bifurcated appearance in our correlation plots. These discrepancies seem to be due to the very low radiation field experienced by the Horsehead PDR and the very clean separation between the PDR environment and a diffuse environment in the NGC 7023 observations.

  7. Dioxins, furans and polycyclic aromatic hydrocarbons emissions from a hospital and cemetery waste incinerator

    Science.gov (United States)

    Mininni, Giuseppe; Sbrilli, Andrea; Maria Braguglia, Camilla; Guerriero, Ettore; Marani, Dario; Rotatori, Mauro

    An experimental campaign was carried out on a hospital and cemetery waste incineration plant in order to assess the emissions of polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs) and polycyclic aromatic hydrocarbons (PAHs). Raw gases were sampled in the afterburning chamber, using a specifically designed device, after the heat recovery section and at the stack. Samples of slags from the combustion chamber and fly ashes from the bag filter were also collected and analyzed. PCDD/Fs and PAHs concentrations in exhaust gas after the heat exchanger (200-350 °C) decreased in comparison with the values detected in the afterburning chamber. Pollutant mass balance regarding the heat exchanger did not confirm literature findings about the de novo synthesis of PCDD/Fs in the heat exchange process. In spite of a consistent reduction of PCDD/Fs in the flue gas treatment system (from 77% up to 98%), the limit of 0.1 ng ITEQ Nm -3 at the stack was not accomplished. PCDD/Fs emission factors for air spanned from 2.3 up to 44 μg ITEQ t -1 of burned waste, whereas those through solid residues (mainly fly ashes) were in the range 41-3700 μg ITEQ t -1. Tests run with cemetery wastes generally showed lower PCDD/F emission factors than those with hospital wastes. PAH total emission factors (91-414 μg kg -1 of burned waste) were in the range of values reported for incineration of municipal and industrial wastes. In spite of the observed release from the scrubber, carcinogenic PAHs concentrations at the stack (0.018-0.5 μg Nm -3) were below the Italian limit of 10 μg Nm -3.

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

    Science.gov (United States)

    Chen, Yingjun; Sheng, Guoying; Bi, Xinhui; Feng, Yanli; Mai, Bixian; Fu, Jiamo

    2005-03-15

    Emission factors of carbonaceous particles, including black carbon (BC) and organic carbon (OC), and polycyclic aromatic hydrocarbons (PAHs) were determined for five coals, which ranged in maturity from sub-bituminous to anthracite. They were burned in the form of honeycomb briquettes in a residential coalstove, one of the most common fuel/stove combinations in China. Smoke samples were taken through dilution sampling equipment, with a high volume sampler that could simultaneously collect emissions in both particulate and gaseous phases, and a cascade impactor that could segregate particles into six fractions. Particulate BC and OC were analyzed by a thermal-optical method, and PAHs in emissions of both phases were analyzed by GC-MS. Burning of bituminous coals produced the highest emission factors of particulate matter (12.91 g/kg), BC (0.28 g/kg), OC (7.82 g/kg), and 20 PAHs (210.6 mg/kg) on the basis of burned dry ash-free (daf) coal, while the anthracite honeycomb-briquette was the cleanest household coal fuel. The size-segregated results show that more than 94% of the particles were submicron, and calculated mass median aerodynamic diameters (MMAD) of all particles were under 0.3 microm. Based on the coal consumption in the residential sector of China, 290.24 Gg (gigagrams) of particulate matter, 5.36 Gg of BC, 170.33 Gg of OC, and 4.72 Gg of 20 PAHs mass were emitted annually from household honeycomb-briquette burning during 2000. Anthracite coal should be selected preferentially and more advanced burning conditions should be applied in domestic combustion, from the viewpoint of both climate change and adverse health effects.

  9. Time resolved spectra in the infrared absorption and emission from shock heated hydrocarbons. [in interstellar medium

    Science.gov (United States)

    Bauer, S. H.; Borchardt, D. B.

    1990-01-01

    The wavelength range of a previously constructed multichannel fast recording spectrometer was extended to the mid-infrared. With the initial configuration, light intensities were recorded simultaneously with a silicon-diode array simultaneously at 20 adjacent wavelengths, each with a 20-micron time resolution. For studies in the infrared, the silicon diodes were replaced by a 20-element PbSe array of similar dimensions, cooled by a three-stage thermoelectric device. It is proposed that infrared emissions could be due to shock-heated low molecular-weight hydrocarbons. The full Swan band system appeared in time-integrated emission spectra from shock-heated C2H2; no soot was generated. At low resolution, the profiles on the high-frequency side of the black body maximum show no distinctive features. These could be fitted to Planck curves, with temperatures that declined with time from an initial high that was intermediate between T5 (no conversion) and T5(eq).

  10. Decentralized production of hydrogen from hydrocarbons with reduced CO{sub 2} emission

    Energy Technology Data Exchange (ETDEWEB)

    Nazim Muradov; Franklyn Smith; Cunping Huang; Ali T-Raissi [Florida Solar Energy Center, University of Central Florida, Cocoa, Florida, (United States)

    2006-07-01

    Currently, most of the industrial hydrogen production is based on steam methane reforming process that releases significant amount of CO{sub 2} into the atmosphere. CO{sub 2} sequestration is one approach to solving the CO{sub 2} emission problem for large centralized hydrogen plants, but it would be impractical for decentralized H{sub 2} production units. The objective of this paper is to explore new routes to hydrogen production from natural gas without (or drastically reduced) CO{sub 2} emissions. One approach analyzed in this paper is based on thermo-catalytic decomposition (TCD) of hydrocarbons (e.g., methane) to hydrogen gas and elemental carbon. The paper discusses some technological aspects of the TCD process development: (1) thermodynamic analysis of TCD using AspenPlus chemical process simulator, (2) heat input options to the endothermic process, (3) catalyst activity issues, etc. Production of hydrogen and carbon via TCD of methane was experimentally verified using carbon-based catalysts. (authors)

  11. Hydrocarbons peaks at Weybourne: What role do natural gas emissions play in the regional background?

    Science.gov (United States)

    Jacob, M. J.; Fleming, Z. L.; Monks, P. S.; Hulse, A.; Oram, D.; Bandy, B. J.; Penkett, S. A.; Hamilton, J. F.; Hopkins, J. R.

    2009-04-01

    Detailed chemical measurements were carried out during the TORCH II (Tropospheric ORganic CHemistry Experiment) campaign at the Weybourne Atmospheric Observatory on the north coast of Norfolk, UK in May 2004. On a number of occasions, large short-lived concentrations of alkenes were observed that correlated with CO, acetaldehyde, HCHO and some alkanes. Foremost was propene, which indicated to have come from emissions from oil and natural gas industries in the North Sea. Simultaneously, a sharp increase in peroxy radicals was observed (from ozone alkene reactions that also produced secondary species such as alkyl nitrates) and subsequent ozone destruction. These emission events were marked by O3 reduction with no corresponding NOy peaks but with extremely high levels of alkene and alkyl nitrates, implying the formation of large levels of peroxy radicals, leading to oxidation consequences in this clean marine environment. Steady state modelling to calculate OH and RO2 values during the episodes revealed that the only source of such high OH and ROx was the ozonolysis of propene. An air mass origin study linked the hydrocarbon peaks with northerly air masses, over the path of known North Sea oil and gas fields. Analysis of VOC measurements at Weybourne during the past 15 years reveals the frequency of such VOC spikes and the impact they could have on photochemical ozone production when they to occur during the daytime and ozone-alkene reactions at nighttime.

  12. High-pressure vapor-phase hydrodeoxygenation of lignin-derived oxygenates to hydrocarbons by a PtMo bimetallic catalyst: Product selectivity, reaction pathway, and structural characterization

    Energy Technology Data Exchange (ETDEWEB)

    Yohe, Sara L.; Choudhari, Harshavardhan J.; Mehta, Dhairya D.; Dietrich, Paul J.; Detwiler, Michael D.; Akatay, Cem M.; Stach, Eric A.; Miller, Jeffrey T.; Delgass, W. Nicholas; Agrawal, Rakesh; Ribeiro, Fabio H.

    2016-12-01

    High-pressure, vapor-phase, hydrodeoxygenation (HDO) reactions of dihydroeugenol (2-methoxy-4-propylphenol), as well as other phenolic, lignin-derived compounds, were investigated over a bimetallic platinum and molybdenum catalyst supported on multi-walled carbon nanotubes (5%Pt2.5%Mo/MWCNT). Hydrocarbons were obtained in 100% yield from dihydroeugenol, including 98% yield of the hydrocarbon propylcyclohexane. The final hydrocarbon distribution was shown to be a strong function of hydrogen partial pressure. Kinetic analysis showed three main dihydroeugenol reaction pathways: HDO, hydrogenation, and alkylation. The major pathway occurred via Pt catalyzed hydrogenation of the aromatic ring and methoxy group cleavage to form 4-propylcyclohexanol, then Mo catalyzed removal of the hydroxyl group by dehydration to form propylcyclohexene, followed by hydrogenation of propylcyclohexene on either the Pt or Mo to form the propylcyclohexane. Transalkylation by the methoxy group occurred as a minor side reaction. Catalyst characterization techniques including chemisorption, scanning transmission electron microscopy, X-ray absorption spectroscopy, and X-ray photoelectron spectroscopy were employed to characterize the catalyst structure. Catalyst components identified were Pt particles, bimetallic PtMo particles, a Mo carbide-like phase, and Mo oxide phases.

  13. Impact of Hydrocarbon Control in Ultraviolet-Assisted Restoration Process for Extremely Porous Plasma Enhanced Chemical Vapor Deposition SiOCH Films with k = 2.0

    Science.gov (United States)

    Kimura, Yosuke; Ishikawa, Dai; Nakano, Akinori; Kobayashi, Akiko; Matsushita, Kiyohiro; de Roest, David; Kobayashi, Nobuyoshi

    2012-05-01

    We investigated the effects of UV-assisted restoration on porous plasma-enhanced chemical vapor deposition (PECVD) SiOCH films with k = 2.0 and 2.3 having high porosities. By applying the UV-assisted restoration to O2-plasma-damaged films with k = 2.0 and 2.3, the recovery of the k-value was observed on the k = 2.3 film in proportion to -OH group reduction. However, the k = 2.0 film did not show recovery in spite of -OH group reduction. We found that hydrocarbon content in the k = 2.0 film was significantly increased by the UV-assisted restoration compared with the k = 2.3 film. According to these findings, we optimized the UV-assisted restoration to achieve improved controllability of the hydrocarbon uptake in the k = 2.0 film and confirmed the recovery of the k-value for O2-plasma-damaged film. Thus, adjusting the hydrocarbon uptake was crucial for restoring extremely porous SiOCH film.

  14. Characteristics of stimulated emission from optically pumped freestanding GaN grown by hydride vapor-phase epitaxy

    CERN Document Server

    Lee, M H; Kim, S T; Chung, S H; Moon, D C

    1999-01-01

    In this study, we observed optically pumped stimulated emission at room temperature in quasi-bulk GaN prepared from thick-film GaN grown on a sapphire substrate by using hydride vapor-phase epitaxy and subsequent mechanical removal of the sapphire substrate. The stimulated emission from the surface and 1-mm-wide-cleaved cavity of the GaN was red-shifted compared to the spontaneous emission by increasing the optical pumping-power density, and the full width at half maximum (FWHM) of the peak decreased. The stimulated emission was demonstrated to have a highly TE-mode polarized nature, and the super-linear dependence of the integrated emission intensity on the excitation power indicated a threshold pump-power density of I sub t sub h = 2 MW/cm sup 2 for one set of stimulated emissions.

  15. Remote measurement of high preeruptive water vapor emissions at Sabancaya volcano by passive differential optical absorption spectroscopy

    Science.gov (United States)

    Kern, Christoph; Masias, Pablo; Apaza, Fredy; Reath, Kevin; Platt, Ulrich

    2017-01-01

    Water (H2O) is by far the most abundant volcanic volatile species and plays a predominant role in driving volcanic eruptions. However, numerous difficulties associated with making accurate measurements of water vapor in volcanic plumes have limited their use as a diagnostic tool. Here we present the first detection of water vapor in a volcanic plume using passive visible-light differential optical absorption spectroscopy (DOAS). Ultraviolet and visible-light DOAS measurements were made on 21 May 2016 at Sabancaya Volcano, Peru. We find that Sabancaya's plume contained an exceptionally high relative water vapor abundance 6 months prior to its November 2016 eruption. Our measurements yielded average sulfur dioxide (SO2) emission rates of 800–900 t/d, H2O emission rates of around 250,000 t/d, and an H2O/SO2 molecular ratio of 1000 which is about an order of magnitude larger than typically found in high-temperature volcanic gases. We attribute the high water vapor emissions to a boiling-off of Sabancaya's hydrothermal system caused by intrusion of magma to shallow depths. This hypothesis is supported by a significant increase in the thermal output of the volcanic edifice detected in infrared satellite imagery leading up to and after our measurements. Though the measurement conditions encountered at Sabancaya were very favorable for our experiment, we show that visible-light DOAS systems could be used to measure water vapor emissions at numerous other high-elevation volcanoes. Such measurements would provide observatories with additional information particularly useful for forecasting eruptions at volcanoes harboring significant hydrothermal systems.

  16. On the Origin of Light Emission in Silicon Rich Oxide Obtained by Low-Pressure Chemical Vapor Deposition

    Directory of Open Access Journals (Sweden)

    M. Aceves-Mijares

    2012-01-01

    Full Text Available Silicon Rich Oxide (SRO has been considered as a material to overcome the drawbacks of silicon to achieve optical functions. Various techniques can be used to produce it, including Low-Pressure Chemical Vapor Deposition (LPCVD. In this paper, a brief description of the studies carried out and discussions of the results obtained on electro-, cathode-, and photoluminescence properties of SRO prepared by LPCVD and annealed at 1,100°C are presented. The experimental results lead us to accept that SRO emission properties are due to oxidation state nanoagglomerates rather than to nanocrystals. The emission mechanism is similar to Donor-Acceptor decay in semiconductors, and a wide emission spectrum, from 450 to 850 nm, has been observed. The results show that emission is a function of both silicon excess in the film and excitation energy. As a result different color emissions can be obtained by selecting the suitable excitation energy.

  17. Strong emissive nanofibers of organogels for the detection of volatile acid vapors.

    Science.gov (United States)

    Xue, Pengchong; Sun, Jiabao; Yao, Boqi; Gong, Peng; Zhang, Zhenqi; Qian, Chong; Zhang, Yuan; Lu, Ran

    2015-03-16

    Two L-phenylalanine derivatives with 5,8-bis(2-(carbazol-3-yl)vinyl)quinoxaline (PCQ) and 5,8-bis[2-(carbazol-3-yl)]-2,3-dimethylquinoxaline (DCQ) as fluorophores were synthesized, and their photophysical properties were measured and compared. The two compounds were found to gelate some organic solvents and self-assemble into 1D nanofibers in gels. The wet gel of PCQ emitted a weak orange fluorescence, but the DCQ gel had a strong green one. This result can be due to the presence of two methyl groups and the nonplanar conformation of fluorophore in DCQ. The gel film of DCQ also showed significantly stronger fluorescence than that of PCQ. Thus, the wet gel and xerogel film of DCQ were selected to study their sensing properties to acids. The yellow wet gel of DCQ transformed into a brown sol upon the addition of 0.2 equiv trifluoroacetic acid (TFA), accompanied by emission quenching. The xerogel film of DCQ rapidly responded to volatile acids, such as TFA, HCl, and HOAc. The fluorescence of the xerogel film was gradually quenched with increased concentration of volatile acid vapors. The fibrous film exhibited low detection limits for volatile acid. The detection limits of the thin films for TFA, HCl, and HOAc reached 43, 122, and 950 ppb, respectively.

  18. Absolute and relative emissions analysis in practical combustion systems—effect of water vapor condensation

    Science.gov (United States)

    Richter, J. P.; Mollendorf, J. C.; DesJardin, P. E.

    2016-11-01

    Accurate knowledge of the absolute combustion gas composition is necessary in the automotive, aircraft, processing, heating and air conditioning industries where emissions reduction is a major concern. Those industries use a variety of sensor technologies. Many of these sensors are used to analyze the gas by pumping a sample through a system of tubes to reach a remote sensor location. An inherent characteristic with this type of sampling strategy is that the mixture state changes as the sample is drawn towards the sensor. Specifically, temperature and humidity changes can be significant, resulting in a very different gas mixture at the sensor interface compared with the in situ location (water vapor dilution effect). Consequently, the gas concentrations obtained from remotely sampled gas analyzers can be significantly different than in situ values. In this study, inherent errors associated with sampled combustion gas concentration measurements are explored, and a correction methodology is presented to determine the absolute gas composition from remotely measured gas species concentrations. For in situ (wet) measurements a heated zirconium dioxide (ZrO2) oxygen sensor (Bosch LSU 4.9) is used to measure the absolute oxygen concentration. This is used to correct the remotely sampled (dry) measurements taken with an electrochemical sensor within the remote analyzer (Testo 330-2LL). In this study, such a correction is experimentally validated for a specified concentration of carbon monoxide (5020 ppmv).

  19. Polycyclic aromatic hydrocarbons (PAHs) from coal combustion: emissions, analysis, and toxicology.

    Science.gov (United States)

    Liu, Guijian; Niu, Zhiyuan; Van Niekerk, Daniel; Xue, Jian; Zheng, Liugen

    2008-01-01

    Coal may become more important as an energy source in the 21st century, and coal contains large quantities of organic and inorganic matter. When coal burns chemical and physical changes take place, and many toxic compounds are formed and emitted. Polycyclic aromatic hydrocarbons (PAHs) are among those compounds formed and are considered to pose potential health hazards because some PAHs are known carcinogens. Based on their toxicology, 16 PAHs are considered as priority pollutants by the USEPA. More attention must be given to the various methods of extraction and analysis of PAH from coal or coal products to accurately explain and determine the species of PAHs. The influences of the extraction time, solvents, and methods for PAH identification are important. In the future, more methods and influences will be studied more carefully and widely. PAHs are environmental pollutants, are highly lipid soluble, and can be absorbed by the lungs, gut, and skin of mammals because they are associated with fine particles from coal combustion. More attention is being given to PAHs because of their carcinogenic and mutagenic action. We suggest that when using a coal stove indoors, a chimney should be used; the particles and gas containing PAHs should be released outdoors to reduce the health hazard, especially in Southwest China. During coal utilization processes, such as coal combustion and pyrolysis, PAHs released may be divided into two categories according to their formation pathways: one pathway is derived from complex chemical reactions and the other is from free PAHs transferred from the original coal. The formation and emission of PAHs is a complex physical and chemical process that has received considerable attention in recent years. It is suggested that the formation mechanisms of PAHs will be an increasingly important topic for researchers to find methods for controlling emissions during coal combustion.

  20. Emissions of polyciclic aromatic hydrocarbons and polyciclic carbonyl biphenils from electric arc furnaces

    Directory of Open Access Journals (Sweden)

    P. Gomes, J. F.

    2008-06-01

    Full Text Available This paper describes work done in order to determine the emissions of highly toxic organic micropollutants from electric arc furnaces used in the production of carbon steel from scrap. The study will be allowing to derive relationships between the levels of airborne micropollutants and the operational parameters of the production process so that an abatement of pollution could be achieved. By using the European standard method CEN 1948 for dioxin like compounds sampling and measurement, it was possible to determine the characteristic fingerprint of micropollutants such as polyciclic aromatic hydrocarbons (PAHs and polycyclic carbonyl biphenils (PCBs emitted by this particular stationary source.

    Este artículo contiene resultados del trabajo ejecutado para estudiar la determinación de las emisiones de los micropolutantes orgánicos muy tóxicos que se emiten por los hornos eléctricos de arco utilizados en la producción de acero. Este estudio inicial va a permitir relacionar las concentraciones de polutantes emitidos a la atmósfera con las condiciones de operación del horno eléctrico de arco. Utilizando el método normalizado CEN 1948 para captación y análisis de muestras de compuestos análogos a las dioxinas ha sido posible determinar el perfil característico de los micropolutantes tales como PAHs y PCBs emitidos por esta fuente.

  1. Severe aromatic hydrocarbon pollution in the Arctic town of Longyearbyen (Svalbard) caused by snowmobile emissions.

    Science.gov (United States)

    Reimann, Stefan; Kallenborn, Roland; Schmidbauer, Norbert

    2009-07-01

    The aromatic hydrocarbons benzene, toluene and C2-benzenes (ethyl benzene and m,p,o-xylene) (BTEX) were measured during a 2-month monitoring campaign in 2007 in the Arctic town of Longyearbyen (Spitsbergen, Svalbard). Reflecting the remoteness of the location, very low mixing ratios were observed during night and in windy conditions. In late spring (April-May), however, the high frequency of guided snowmobile tours resulted in "rush-hour" maximum values of more than 10 ppb of BTEX. These concentration levels are comparable to those in European towns and are caused predominately by the outdated 2-stroke engines, which are still used by approximately 30% of the snowmobiles in Longyearbyen. During summer, peak events were about a factor of 100 lower compared to those during the snowmobile season. Emissions in summer were mainly caused by diesel-fueled heavy duty vehicles (HDVs), permanently used for coal transport from the adjacent coal mines. The documented high BTEX mixing ratios from snowmobiles in the Arctic provide an obvious incentive to change the regulation practice to a cleaner engine technology.

  2. Hydrocarbon emissions and characterization of methane sources in the Barnett Shale

    Science.gov (United States)

    Marrero, J. E.; Townsend-Small, A.; Meinardi, S.; Blake, D. R.

    2014-12-01

    As energy demand and costs continue to rise worldwide, so does the development of energy from natural gas. The United States in particular has expanded its natural gas industry, becoming one of the world's top gas producing countries. The Barnett Shale of northern Texas is one of the most developed and productive natural gas shale plays in the United States. However, emissions from the many oil and gas system components in the region have not been fully characterized. An extensive list of volatile organic compounds (VOCs) was measured from 120 whole air canisters collected throughout the Barnett shale in October 2013. Known methane sources were targeted and included oil and natural gas well pads, compressor stations, distribution pipelines and city gates, cattle feedlots and landfills. C1-C5 alkanes were elevated throughout the region and were similar to or greater than concentrations in major U.S. cities. The VOC source signature for oil and gas operations was distinguished from biogenic sources. Average ethane content relative to methane was calculated for each of the source types, and ranged from 0.7 to 12.8%. For the whole region, the ethane content was 7.2±6.1%, illustrating the high variability and effect of the various hydrocarbon sources on the local air.

  3. Process Design and Economics for the Conversion of Lignocellulosic Biomass to Hydrocarbon Fuels. Thermochemical Research Pathways with In Situ and Ex Situ Upgrading of Fast Pyrolysis Vapors

    Energy Technology Data Exchange (ETDEWEB)

    Dutta, A.; Sahir, A.; Tan, E.; Humbird, D.; Snowden-Swan, L. J.; Meyer, P.; Ross, J.; Sexton, D.; Yap, R.; Lukas, J.

    2015-03-01

    This report was developed as part of the U.S. Department of Energy’s Bioenergy Technologies Office’s efforts to enable the development of technologies for the production of infrastructurecompatible, cost-competitive liquid hydrocarbon fuels from biomass. Specifically, this report details two conceptual designs based on projected product yields and quality improvements via catalyst development and process integration. It is expected that these research improvements will be made within the 2022 timeframe. The two conversion pathways detailed are (1) in situ and (2) ex situ upgrading of vapors produced from the fast pyrolysis of biomass. While the base case conceptual designs and underlying assumptions outline performance metrics for feasibility, it should be noted that these are only two of many other possibilities in this area of research. Other promising process design options emerging from the research will be considered for future techno-economic analysis.

  4. Vapor Extraction/Bioventing Sequential Treatment of Soil Contaminated with Volatile and SemiVolatile Hydrocarbon Mixtures

    NARCIS (Netherlands)

    Malina, G.; Grotenhuis, J.T.C.; Rulkens, W.H.

    2002-01-01

    A cost-effective removal strategy was studied in bench-scale columns that involved vapor extraction and bioventing sequential treatment of toluene- and decane-contaminated soil. The effect of operating mode on treatment performance was examined at a continuous air flow and consecutively at two diffe

  5. The effects of biodiesel and its blends with diesel oil on the emission of volatile aromatic hydrocarbons

    Directory of Open Access Journals (Sweden)

    Adam Prokopowicz

    2013-12-01

    Full Text Available Background: In recent times, the emphasis is placed on the use of renewable fuels as well as biodiesel as an attractive alternative to conventional diesel fuel. Due to the fact that the impact of biodiesel on various chemical compounds exhaust emissions is not completely characterized, we have evaluated the emissions of volatile aromatic hydrocarbons in relation to biodiesel content in conventional diesel fuel. Material and methods: In the study we have assessed the emission of benzene, toluene, ethylbenzene and xylens during New European Driving Cycle NEDC for a passenger car with a diesel engine using the following fuels: 100% diesel fuel (B0, 100% rapeseed methyl esters (B100, 7, 15 and 30% rapeseed methyl esters in diesel fuel (B7, B15, B30, and 30% hydrotreated vegetable oil in diesel fuel (HVO30. Results: Among all determined compounds, benzene and toluene were emitted in the largest quantities. Higher emissions were determined during urban driving cycle then during extraurban driving cycle. A clear trend was observed when along with increasing amount of added rapeseed methyl esters the emission increased. However, additive of HVO decreased the emission of the most volatile aromatic compounds even when compared to conventional diesel fuel. During extra-urban driving cycle the emission was significantly lower and comparable for most fuels tested. Nevertheless in the context of conventional diesel fuel, lower emission for fuels with biodiesel was observed. Conclusion: The results have indicated the increase in benzene and toluene exhaust emissions mostly during urban driving cycle and its decrease during extra-urban driving cycle in NEDC test with increasing content of fatty acids methyl esters in diesel fuel. The emission in urban cycle was probably influenced by cold-start condition during this cycle. Generation of volatile aromatic hydrocarbons may be related to higher density of fuel with biodiesel in comparison to density of diesel oil

  6. The relationship between gasoline composition and vehicle hydrocarbon emissions: a review of current studies and future research needs.

    Science.gov (United States)

    Schuetzle, D; Siegl, W O; Jensen, T E; Dearth, M A; Kaiser, E W; Gorse, R; Kreucher, W; Kulik, E

    1994-01-01

    The purpose of this paper is to review current studies concerning the relationship of fuel composition to vehicle engine-out and tail-pipe emissions and to outline future research needed in this area. A number of recent combustion experiments and vehicle studies demonstrated that reformulated gasoline can reduce vehicle engine-out, tail-pipe, running-loss, and evaporative emissions. Some of these studies were extended to understand the fundamental relationships between fuel composition and emissions. To further establish these relationships, it was necessary to develop advanced analytical methods for the qualitative and quantitative analysis of hydrocarbons in fuels and vehicle emissions. The development of real-time techniques such as Fourier transform infrared spectroscopy, laser diode spectroscopy, and atmospheric pressure ionization mass spectrometry were useful in studying the transient behavior of exhaust emissions under various engine operating conditions. Laboratory studies using specific fuels and fuel blends were carried out using pulse flame combustors, single- and multicylinder engines, and vehicle fleets. Chemometric statistical methods were used to analyze the large volumes of emissions data generated from these studies. Models were developed that were able to accurately predict tail-pipe emissions from fuel chemical and physical compositional data. Some of the primary fuel precursors for benzene, 1,3-butadiene, formaldehyde, acetaldehyde and C2-C4 alkene emissions are described. These studies demonstrated that there is a strong relationship between gasoline composition and tail-pipe emissions. PMID:7529705

  7. Potential of Solid Sampling Electrothermal Vaporization for solving spectral interference in Inductively Coupled Plasma Optical Emission Spectrometry

    Science.gov (United States)

    Asfaw, Alemayehu; Wibetoe, Grethe

    2009-05-01

    Spectral interference is one of the main causes of erroneous results in Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES). This paper describes some cases of spectral interferences with conventional nebulization ICP-OES and the potential of solving them utilizing electrothermal vaporization for volatility-based separation. The cases studied were, the well-known spectral overlap between the As and Cd lines at 228.8 nm that are only 10 pm apart, and the interference of Fe on the main emission lines of As, Cd and Pb. The spectral interferences were studied by monitoring the typical signals of solutions that contain the analytes and the potential interferent, by studying the spectra and calculating Background Equivalent Concentration (BEC)-values. A three step temperature program was developed to be used for direct analysis of solid soil samples by Electrothermal Vaporization (ETV)-ICP-OES: step 1 (760 °C, 40 s), step 2 (1620 °C, 20 s) and a cleaning step (2250 °C, 10 s) where Cd vaporizes in step 1, As, Pb and part of Fe in step 2 and the major part of Fe in the cleaning step. Because As and Cd were time-separated using this program, their prominent lines at 228.8 nm, could be used for determination of each element by ETV-ICP-OES, in spite of the serious wavelength overlap. Selective vaporization was also shown to reduce or eliminate the Fe background emission on As, Cd and Pb lines. To confirm the applicability of the method, a solid soil certified reference materials was analyzed directly without any sample treatment. Good or reasonable accuracy was obtained for the three elements.

  8. The use Na, Li, K cations for modification of ZSM-5 zewolite to control hydrocarbon cold-start emission

    Energy Technology Data Exchange (ETDEWEB)

    Golubeva V.; Rohatgi U.; Korableva, A.; Anischenko, O.; Kustov, L.; Nissenbaum, V; Viola, M.B.

    2012-08-29

    This paper addresses the problem of controlling hydrocarbon emissions from cold-start of engines by investigating the adsorbents which could adsorb the hydrocarbons at cold temperatures and hold them to 250-300 ?. The materials, that has been studied, are based on the modification of ZSM-5 (SiO{sub 2}/Al{sub 2}O{sub 3} = 35) zeolite with Li, K, Na cations. It has been shown that the introduction of Li, Na and K in an amount that is equivalent to the content of Al in zeolite results in occurrence of toluene temperature desorption peaks at high-temperatures. The toluene temperature desorption curves for 5%Li-ZSM-5 and 2.3%Na-ZSM-5 zeolites are identical and have peak toluene desorption rate between 200 to 400 ?. Upon analysis of toluene adsorption isotherms for 2.3%Na-ZSM-5 and 5%Li-ZSM-5, it was concluded that the toluene diffusion inside of the modified zeolites channels is extremely slow and the sorption capacity of 2.3%Na-ZSM-5 is higher than with 5%Li-ZSM-5. The 2.3%Na-ZSM-5 didn't change toluene temperature programmed desorption (TPD) rate of curve after the treatment in environment with 10% ?{sub 2}? at 750-800 ? for about 28 h. The 2.3%Na-ZSM-5 zeolite is very promising as adsorbent to control the cold-start hydrocarbon emissions.

  9. Vapor-Liquid Equilibrium of Toluene-Polycyclic Aromatic Hydrocarbon System in Sub-and Supercritical State

    Institute of Scientific and Technical Information of China (English)

    Cheol-Joong; KIM; Dong-Bok; WON; 等

    2002-01-01

    The phase behaviors of toluene/polycyclic aromatic hydrocarbon mixture systems were investigated with a continuous-flow type apparatus at 573.2,598.2.623.2 and 648.2K,while the pressure changed from 1 tp 5 MPa,The pseudo-binary phase behaviors were predicted with the Peng-Robinson equation of state with interaction parameters between toluene and pseudo-components considered.The phase diagrams of the system have been classified following the category of phase boundary diagram models.The extraction selectivity and efficiency of toluene as a solvent was discussed by comparing with that of hexane .The prediction model for selectivity was also suggested.

  10. Black carbon and polycyclic aromatic hydrocarbon emissions from vehicles in the United States-Mexico border region: pilot study.

    Science.gov (United States)

    Kelly, Kerry; Wagner, David; Lighty, JoAnn; Quintero Núñez, Margarito; Vazquez, F Adrian; Collins, Kimberly; Barud-Zubillaga, Alberto

    2006-03-01

    The investigators developed a system to measure black carbon (BC) and particle-bound polycyclic aromatic hydrocarbon (PAH) emission factors during roadside sampling in four cities along the United States-Mexico border, Calexico/Mexicali and El Paso/Juarez. The measurement system included a photoacoustic analyzer for BC, a photoelectric aerosol sensor for particle-bound PAHs, and a carbon dioxide (CO2) analyzer. When a vehicle with measurable emissions passed the system probe, corresponding BC, PAH, and CO2 peaks were evident, and a fuel-based emission factor was estimated. A picture of each vehicle was also recorded with a digital camera. The advantage of this system, compared with other roadside methods, is the direct measurement of particulate matter components and limited interference from roadside dust. The study revealed some interesting trends: Mexican buses and all medium-duty trucks were more frequently identified as high emitters of BC and PAH than heavy-duty trucks or passenger vehicles. In addition, because of the high daily mileage of buses, they are good candidates for additional study. Mexican trucks and buses had higher average emission factors compared with U.S. trucks and buses, but the differences were not statistically significant. Few passenger vehicles had measurable BC and PAH emissions, although the highest emission factor came from an older model passenger vehicle licensed in Baja California.

  11. Economic implications of incorporating emission controls to mitigate air pollutants emitted from a modeled hydrocarbon-fuel biorefinery in the United States: Economic implications of air emission controls for a hydrocarbon-fuel biorefinery

    Energy Technology Data Exchange (ETDEWEB)

    Bhatt, Arpit [National Renewable Energy Laboratory, Golden CO USA; Zhang, Yimin [National Renewable Energy Laboratory, Golden CO USA; Davis, Ryan [National Renewable Energy Laboratory, Golden CO USA; Eberle, Annika [National Renewable Energy Laboratory, Golden CO USA; Heath, Garvin [National Renewable Energy Laboratory, Golden CO USA

    2016-07-15

    The implementation of the US Renewable Fuel Standard is expected to increase the construction and operation of new biofuel facilities. Allowing this industry to grow without adversely affecting air quality is an important sustainability goal sought by multiple stakeholders. However, little is known about how the emission controls potentially required to comply with air quality regulations might impact biorefinery cost and deployment strategies such as siting and sizing. In this study, we use a baseline design for a lignocellulosic hydrocarbon biofuel production process to assess how the integration of emission controls impacts the minimum fuel selling price (MFSP) of the biofuel produced. We evaluate the change in MFSP for two cases as compared to the baseline design by incorporating (i) emission controls that ensure compliance with applicable federal air regulations and (ii) advanced control options that could be used to achieve potential best available control technology (BACT) emission limits. Our results indicate that compliance with federal air regulations can be achieved with minimal impact on biofuel cost (~$0.02 per gasoline gallon equivalent (GGE) higher than the baseline price of $5.10 GGE-1). However, if air emissions must be further reduced to meet potential BACT emission limits, the cost could increase nontrivially. For example, the MFSP could increase to $5.50 GGE-1 by adopting advanced emission controls to meet potential boiler BACT limits. Given tradeoffs among emission control costs, permitting requirements, and economies of scale, these results could help inform decisions about biorefinery siting and sizing and mitigate risks associated with air permitting.

  12. Efficiency Analysis of Technological Methods for Reduction of NOx Emissions while Burning Hydrocarbon Fuels in Heat and Power Plants

    Directory of Open Access Journals (Sweden)

    S. Kabishov

    2013-01-01

    Full Text Available The paper contains a comparative efficiency analysis pertaining to application of existing technological methods for suppression of nitric oxide formation in heating boilers of heat generators. A special attention has been given to investigation of NOx  emission reduction while burning hydrocarbon fuel with the help of oxygen-enriched air. The calculations have demonstrated that while enriching oxidizer with the help of oxygen up to 50 % (by volume it is possible to reduce volume of NOx formation (while burning fuel unit by 21 %.

  13. Effects of potassium hydroxide post-treatments on the field-emission properties of thermal chemical vapor deposited carbon nanotubes.

    Science.gov (United States)

    Lee, Li-Ying; Lee, Shih-Fong; Chang, Yung-Ping; Hsiao, Wei-Shao

    2011-12-01

    In this study, a simple potassium hydroxide treatment was applied to functionalize the surface and to modify the structure of multi-walled carbon nanotubes grown on silicon substrates by thermal chemical vapor deposition. Scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, and energy dispersive spectrometry were employed to investigate the mechanism causing the modified field-emission properties of carbon nanotubes. From our experimental data, the emitted currents of carbon nanotubes after potassium hydroxide treatment are enhanced by more than one order of magnitude compared with those of untreated carbon nanotubes. The emitted current density of carbon nanotubes increases from 0.44 mA/cm2 to 7.92 mA/cm2 after 30 minutes KOH treatment. This technique provides a simple, economical, and effective way to enhance the field-emission properties of carbon nanotubes.

  14. PAH emission from Herbig AeBe stars: Do hydrocarbons in proto-planetary disks have a unique aroma?

    Science.gov (United States)

    Keller, Luke; Sloan, Greg

    2008-03-01

    Over half of the intermediate-mass young stellar objects in the Galaxy (e.g. Herbig AeBe stars or HAeBe) have high-contrast emission in the mid-infrared spectral features of polycyclic aromatic hydrocarbons (PAHs) above the continuum produced by thermal emission from dust in the circumstellar disks. We have examined the PAH emission in detail for a sample of 19 HAeBe stars observed with the Spitzer IRS as part of the IRS Disks GTO program. Even with this relatively small sample, we have identified some trends that, should they survive in a larger sample of HAeBe stars, will allow us to infer large-scale disk geometry (both inner and outer) and the degree of photo-processing of organic molecular material in HAeBe disks. The bottom line of our work thus far is that HAeBe apparently have distinctive PAH spectra among the many other astronomical environments that are characterized by strong PAH emission. We therefore propose to apply our spectral analysis methods to an additional 57 HAeBe observed with the IRS and currently (or soon to be) available in the Spitzer archive. Our total sample of 76 HAeBe stars will allow closer scrutiny of the trends that we have identified in our empirical study and will also be the subject of a detailed disk modeling effort that will include the PAH emission.

  15. PAH Emission from Disks around Intermediate-Mass Stars: The Peculiar Aroma of Hydrocarbons Orbiting Herbig Ae/Be Stars

    Science.gov (United States)

    Keller, L. D.; Sloan, G. C.

    2009-12-01

    Over half of the intermediate-mass young stellar objects in the Galaxy (e.g. Herbig Ae/Be stars or HAeBe) have high-contrast emission in the mid-infrared spectral features of polycyclic aromatic hydrocarbons (PAHs) above the continuum produced by thermal emission from dust in the circumstellar disks. We have examined the PAH emission in detail for 30 HAeBe stars observed with the Spitzer IRS. We have identified some trends that, should they survive in a larger sample of HAeBe stars, will allow us to infer large-scale disk geometry (both inner and outer) and the degree of photo-processing of organic molecular material in HAeBe disks: HAeBe stars apparently have distinctive PAH spectra among the many other astronomical environments that are characterized by strong PAH emission; strong PAH emission is not necessarily an indicator of a particular disk geometry; PAH spectra of HAeBe stars change systematically with stellar effective temperature; PAH in HAeBe disks are ionized. As part of a Spitzer archival project we are applying our spectral analysis methods to an even larger sample of HAeBe stars observed with the IRS and currently available in the Spitzer archive. Here we report preliminary results as we begin the larger study.

  16. Estimating Emissions of Toxic Hydrocarbons from Natural Gas Production Sites in the Barnett Shale Region of Northern Texas.

    Science.gov (United States)

    Marrero, Josette E; Townsend-Small, Amy; Lyon, David R; Tsai, Tracy R; Meinardi, Simone; Blake, Donald R

    2016-10-04

    Oil and natural gas operations have continued to expand and move closer to densely populated areas, contributing to growing public concerns regarding exposure to hazardous air pollutants. During the Barnett Shale Coordinated Campaign in October, 2013, ground-based whole air samples collected downwind of oil and gas sites revealed enhancements in several potentially toxic volatile organic compounds (VOCs) when compared to background values. Molar emissions ratios relative to methane were determined for hexane, benzene, toluene, ethylbenzene, and xylene (BTEX compounds). Using methane leak rates measured from the Picarro mobile flux plane (MFP) system and a Barnett Shale regional methane emissions inventory, the rates of emission of these toxic gases were calculated. Benzene emissions ranged between 51 ± 4 and 60 ± 4 kg h(-1). Hexane, the most abundantly emitted pollutant, ranged from 642 ± 45 to 1070 ± 340 kg h(-1). While observed hydrocarbon enhancements fall below federal workplace standards, results may indicate a link between emissions from oil and natural gas operations and concerns about exposure to hazardous air pollutants. The larger public health risks associated with the production and distribution of natural gas are of particular importance and warrant further investigation, particularly as the use of natural gas increases in the United States and internationally.

  17. Emission of polycyclic aromatic hydrocarbons from coal and sewage sludge co-combustion in a drop tube furnace.

    Science.gov (United States)

    Han, Jun; Qin, Linbo; Ye, Wei; Li, Yuqi; Liu, Long; Wang, Hao; Yao, Hong

    2012-09-01

    The emission characteristics of polycyclic aromatic hydrocarbons (PAHs) during coal and sewage sludge co-combustion were investigated in a laboratory-scale drop tube furnace. The experimental results demonstrated that coal and sewage sludge co-combustion was beneficial in reducing PAH emissions and PAH toxic equivalent (TEQ) concentrations. Meanwhile, the five-ring PAHs were the main contributor in reducing the concentration of PAHs and TEQ. Moreover, the two- and five-ring PAH concentrations decreased as the mass fraction of sewage sludge in the mixture increased from 0% to 100%. It was also found that PAHs from coal mono-combustion was dominated by the four- and five-ring PAHs. As for the sewage sludge mono-combustion, the three- and four-ring PAHs were the principal components.

  18. The bulk isotopic composition of hydrocarbons in subaerial volcanic-hydrothermal emissions from different tectonic settings

    Science.gov (United States)

    Fiebig, J.; Tassi, F.; Vaselli, O.; Viveiros, M. F.; Silva, C.; Lopez, T. M.; D'Alessandro, W.; Stefansson, A.

    2015-12-01

    Assuming that methane and its higher chain homologues derive from a common source, carbon isotope patterns have been applied as a criterion to identify occurrences of abiogenic hydrocarbons. Based on these, it has been postulated that abiogenic hydrocarbon production occurs within several (ultra)mafic environments. More evolved volcanic-hydrothermal systems may also provide all the prerequisites necessary for abiogenic hydrocarbon production, such as availability of inorganic CO2, hydrogen and heat. We have investigated the chemical and isotopic composition of n-alkanes contained within subaerial hydrothermal discharges emitted from a range of hot spot, subduction and rift-related volcanoes to determine the origin of hydrocarbons in these systems. Amongst these are Nisyros (Greece), Vesuvio, Campi Flegrei, Ischia, Pantelleria and Vulcano (all Italy), Mt. Mageik and Trident (USA), Copahue (Argentina), Teide (Spain), Furnas and Fogo (Portugal). The carbon isotopic composition of methane emitted from these sites varies from -65 to -8‰ , whereas δ13C of ethane and propane exhibit a much narrower variation from -17‰ to -31‰. Methane that occurs most enriched in 13C is also characterized by relatively positive δD values ranging up to -80‰. Carbon isotope reversals between methane and ethane are only observed for locations exhibiting δ13C-CH4 values > -20‰, such as Teide, Pantelleria, Trident and Furnas. At Furnas, δ13C-CH4 varies by 50‰ within a relatively short distance of <50m between two vents, whereas δ13C-C2H6 varies by less than 2‰ only. For some of the investigated locations apparent carbon isotopic temperatures between methane and CO2 are in agreement with those derived from gas concentration geothermometers. At these locations methane, however seems to be in disequilibrium with ethane and propane. These findings imply that methane on the one hand and the C2+ hydrocarbons on the other hand often might derive from distinct sources.

  19. Characteristics of polycyclic aromatic hydrocarbons and their gas/particle partitioning from fugitive emissions in coke plants

    Science.gov (United States)

    Mu, Ling; Peng, Lin; Liu, Xiaofeng; Song, Chongfang; Bai, Huiling; Zhang, Jianqiang; Hu, Dongmei; He, Qiusheng; Li, Fan

    2014-02-01

    Coking is one of the most important emission sources of polycyclic aromatic hydrocarbons (PAHs) in China. However, there is little information available on the emission characteristics of PAHs from fugitive emission during coking, especially on the specific processes dominating the gas-particle partitioning of PAHs. In this study, emission characteristics and gas-particle partitioning of PAHs from fugitive emission in four typical coke plants (CPs) with different scales and techniques were investigated. The average concentrations of total PAHs from fugitive emission at CP2, CP3 and CP4 (stamp charging) were 146.98, 31.82, and 35.20 μg m-3, which were 13.38-, 2.90- and 3.20-fold higher, respectively, than those at CP1 (top charging, 10.98 μg m-3). Low molecular weight PAHs with 2-3 rings made up 75.3% of the total PAHs on average, and the contributions of particulate PAH to the total BaP equivalent concentrations (BaPeq) in each plant were significantly higher than the corresponding contributions to the total PAH mass concentrations. The calculated total BaPeq concentrations varied from 0.19 to 10.86 μg m-3 with an average of 3.14 μg m-3, and more efficient measures to control fugitive emission in coke plants should be employed to prevent or reduce the health risk to workers. Absorption into organic matter dominated the gas-particle partitioning for most of the PAHs including PhA, FluA, Chr, BbF, BkF and BaP, while adsorption on elemental carbon appeared to play a dominant role for AcPy, AcP and Flu.

  20. Stimulated Emission at 722.9 nm by Laser Photodissociation of PbI2 Vapor

    Institute of Scientific and Technical Information of China (English)

    MAN Bao-Yuan; ZHANG Jie; NI Pei-Gen; ZHANG Dao-Zhong

    2000-01-01

    The stimulated emission at 722.9nm is observed by a direct photodissociation of the PbI2 molecules with a 266nm pulse laser. The possible dissociation channels are discussed. Two-photon resonant photodissociation mechanism is used to explain the generation of the 722.9 nm emission. The emission is measured at different incident laser energy and heat-pipe temperature. The obtained experimental result is well supported by the photodissociation mechanism given by us.

  1. Urban air chemistry and diesel vehicles emissions: Quantifying small and big hydrocarbons by CIMS to improve emission inventories

    Science.gov (United States)

    Jobson, B. T.; Derstroff, B.; Edtbauer, A.; VanderSchelden, G. S.; Williams, J.

    2017-10-01

    Emissions from vehicles are a major source of volatile organic compounds (VOCs) in urban environments. Photochemical oxidation of VOCs emitted from vehicle exhaust contributes to O3 and PM2.5 formation, harmful pollutants that major urban areas struggle to control. How will a shift to a diesel engine fleet impact urban air chemistry? Diesel vehicles are a growing fraction of the passenger vehicle fleet in Europe as a result of a deliberate policy to reduce energy consumption and CO2 emissions from the transportation sector (Sullivan et al., 2004). In countries such as France the diesel passenger fleet was already ∼50% of the total in 2009, up from 20% in 1995. Dunmore et al. (2015) have recently inferred that in London, HO radical loss rates to organic compounds is dominated by diesel engine emissions. In the US, increasingly more stringent vehicles emission standards and requirement for improved energy efficiency means spark ignition passenger vehicle emissions have declined significantly over the last 20 years, resulting in the urban diesel fleet traffic (freight trucks) having a growing importance as a source of vehicle pollution (McDonald et al., 2013). The recent scandal involving a major car manufacturer rigging emission controls for diesel passenger cars is a reminder that real world emissions of VOCs from diesel engines are not well understood nor thoroughly accounted for in air quality modeling.

  2. Mobile Laboratory Measurements of Black Carbon and Polycyclic Aromatic Hydrocarbon Emissions in Mexico City: A New Method for Motor Vehicle Emission Inventory Calculations

    Science.gov (United States)

    Jiang, M.; Marr, L. C.; Dunlea, E.; Herndon, S.; Jayne, J.; Rogers, T.; Knighton, B.; Zavala, M.; Molina, L. T.; Molina, M. J.

    2004-12-01

    Aerosol black carbon (BC) and polycyclic aromatic hydrocarbons (PAHs) are two products of carbonaceous fuel combustion that are of major concern for urban air quality and global climate change. As part of the Mexico City Metropolitan Area field campaign in April 2003 (MCMA-2003), a mobile laboratory drove throughout the city and chased vehicles to measure pollutants in their exhaust emissions. The laboratory is a van designed and built by Aerodyne Research, Inc. and is equipped with a suite of gas and particle analyzers, including an aethalometer that measures BC and a photoemission aerosol sensor that measures particle-bound PAHs. The main goal of this research is to determine fuel-based emission factors, or the mass of BC and PAH emitted per volume of fuel burned, for Mexico City¡_s vehicle fleet. We can then calculate the megacity¡_s emission inventory of these compounds, which is important on both the urban and global scales. In previous analyses, the mobile laboratory has been used to target emissions from specific vehicles. While chasing events can be analyzed to obtain emission factors for specific vehicles, data from the entire time period while the lab is driving through the streets, whether chasing individual vehicles or not, can also provide valuable information about mobile source emissions. The laboratory continuously samples ambient air from an inlet at the front of the van, and it is always ¡°seeing¡± exhaust plumes from the vehicles around it. This ¡°macroscopic¡± approach that considers all vehicles on the road, similar to tunnel and remote sensing studies, complements the ¡°microscopic¡± approach that focuses on individual vehicles. We have developed a method that automatically identifies exhaust plumes and quantifies emission factors from data collected by the mobile lab. While 200 individual chasing events were identified during the field campaign, over 40,000 exhaust plume points were identified using the macroscopic approach. The

  3. Accumulation of polycyclic aromatic hydrocarbons (PAHs) on the spider webs in the vicinity of road traffic emissions.

    Science.gov (United States)

    Rybak, Justyna; Olejniczak, Teresa

    2014-02-01

    Studies focused on the possible use of spider webs as environmental pollution indicators. This was a first time ever attempt to use webs as indicators of polycyclic aromatic hydrocarbons (PAHs) pollution. The aim of the study was (a) to evaluate whether webs are able to accumulate PM-associated road traffic emissions and be analyzed for organic toxics such as PAHs, (b) to assess if the distance from emission sources could have an influence on the accumulation level of pollutants, and (c) to determine types of pollution sources responsible for a structure of monitoring data set. Webs of four species from the family Agelenidae were sampled for PAHs presence. Data from vehicle traffic sites (i.e., road tunnel, arterial surface road, underground parking) and from railway traffic sites (i.e., two railway viaducts) in the city of Wroclaw (Southwest of Poland) showed a significantly higher mean concentrations of PAHs than the reference site 1 (municipal water supply works). We also found a significant differences at sites differed by the distance from emission sources. The result of PCA analysis suggested three important sources of pollution. We conclude that spider webs despite of some limitations proved useful indicators of road traffic emissions; they could be even more reliable compared to use of bioindicators whose activity is often limited by a lack of water and sun.

  4. Vehicle fleet emissions of black carbon, polycyclic aromatic hydrocarbons, and other pollutants measured by a mobile laboratory in Mexico City

    Directory of Open Access Journals (Sweden)

    M. Jiang

    2005-01-01

    Full Text Available Black carbon (BC and polycyclic aromatic hydrocarbons (PAHs are of concern due to their effects on climate and health. The main goal of this research is to provide the first estimate of emissions of BC and particle-phase PAHs (PPAHs from motor vehicles in Mexico City. The emissions of other pollutants including carbon monoxide (CO, oxides of nitrogen (NOx, volatile organic compounds (VOCs, and particulate matter of diameter 2.5 μm and less (PM2.5 are also estimated. As a part of the Mexico City Metropolitan Area field campaign in April 2003 (MCMA-2003, a mobile laboratory was driven throughout the city. The laboratory was equipped with a comprehensive suite of gas and particle analyzers, including an aethalometer that measured BC and a photoionization aerosol sensor that measured PPAHs. While driving through traffic, the mobile lab continuously sampled exhaust plumes from the vehicles around it. We have developed a method of automatically identifying exhaust plumes, which are then used as the basis for calculation of fleet-average emissions. In the approximately 75 h of on-road sampling during the field campaign, we have identified ~30 000 exhaust measurement points that represent a variety of vehicle types and driving conditions. The large sample provides a basis for estimating fleet-average emission factors and thus the emission inventory. Motor vehicles in the Mexico City area are estimated to emit 1700±200 metric tons BC, 57±6 tons PPAHs, 1 190 000±40 000 tons CO, 120 000±3000 tons NOx, 240 000±50 000 tons VOCs, and 4400±400 tons PM2.5 per year, not including cold start emissions. The estimates for CO, NOx, and PPAHs may be low by up to 10% due to the slower response time of analyzers used to measure these species. Compared to the government's official motor vehicle emission inventory for the year 2002, the estimates for CO, NOx, VOCs, and PM2.5 are 38% lower, 23% lower, 27% higher, and 25% higher, respectively. The

  5. Characterization of polycyclic aromatic hydrocarbon emissions in the particulate phase from burning incenses with various atomic hydrogen/carbon ratios

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Tzu-Ting, E-mail: d89844001@ntu.edu.tw [Department of Environmental Engineering and Health, Yuanpei University, No. 306, Yuanpei St., Hsin Chu, 300, Taiwan (China); Lin, Shaw-Tao [Department of Applied Chemistry, Providence University, 200 Chung-Chi Rd., Salu Dist., Taichung City 43301, Taiwan (China); Lin, Tser-Sheng [Department of Safety, Health, and Environmental Engineering, National United University, 2 Lien Da, Maioli, 360, Taiwan (China); Hong, Wei-Lun [Department of Environmental Engineering and Health, Yuanpei University, No. 306, Yuanpei St., Hsin Chu, 300, Taiwan (China)

    2012-01-01

    Polycyclic aromatic hydrocarbons in the particulate phase generated from burning various incense was investigated by a gas chromatography/mass spectrometry. Among the used incenses, the atomic H/C ratio ranged from 0.51 to 1.69, yielding the emission factor ranges for total particulate mass and PAHs of 4.19-82.16 mg/g and 1.20-9.50 {mu}g/g, respectively. The atomic H/C ratio of the incense was the key factor affecting particulate mass and the PAHs emission factors. Both the maximum emission factor and the slowest burning rate appear at the H/C ratio of 1.57. The concentrations of the four-ring PAHs predominated and the major species among the 16 PAHs were fluoranthene, phenanthrene, pyrene, and chrysene for most incense types. The benzo[a]pyrene, benzo[a]anthracene, benzo[b]fluoranthene, and dibenzo[a,h]anthracene accounted for 87.08-93.47% of the total toxic equivalency emission factor. - Highlights: Black-Right-Pointing-Pointer The atomic H/C ratio of incense was the key factor affecting PAHs emission factors. Black-Right-Pointing-Pointer Burning incense with lower atomic H/C ratio minimized the production of total PAHs. Black-Right-Pointing-Pointer The BaP, BaA, BbF, and DBA accounted for 87.08-93.47% of the TEQ emission factor. Black-Right-Pointing-Pointer Special PAH ratios were regarded as characteristic ratios for burning incense.

  6. Process Design and Economics for the Conversion of Lignocellulosic Biomass to Hydrocarbon Fuels: Thermochemical Research Pathways with In Situ and Ex Situ Upgrading of Fast Pyrolysis Vapors

    Energy Technology Data Exchange (ETDEWEB)

    Dutta, Abhijit [National Renewable Energy Lab. (NREL), Golden, CO (United States); Sahir, A. H. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Tan, Eric [National Renewable Energy Lab. (NREL), Golden, CO (United States); Humbird, David [DWH Process Consulting, Denver, CO (United States); Snowden-Swan, Lesley J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Meyer, Pimphan A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Ross, Jeff [Harris Group, Inc., Seattle, WA (United States); Sexton, Danielle [Harris Group, Inc., Seattle, WA (United States); Yap, Raymond [Harris Group, Inc., Seattle, WA (United States); Lukas, John [Harris Group, Inc., Seattle, WA (United States)

    2015-03-01

    This report was developed as part of the U.S. Department of Energy’s Bioenergy Technologies Office’s efforts to enable the development of technologies for the production of infrastructure-compatible, cost-competitive liquid hydrocarbon fuels from biomass. Specifically, this report details two conceptual designs based on projected product yields and quality improvements via catalyst development and process integration. It is expected that these research improvements will be made within the 2022 timeframe. The two conversion pathways detailed are (1) in situ and (2) ex situ upgrading of vapors produced from the fast pyrolysis of biomass. While the base case conceptual designs and underlying assumptions outline performance metrics for feasibility, it should be noted that these are only two of many other possibilities in this area of research. Other promising process design options emerging from the research will be considered for future techno-economic analysis. Both the in situ and ex situ conceptual designs, using the underlying assumptions, project MFSPs of approximately $3.5/gallon gasoline equivalent (GGE). The performance assumptions for the ex situ process were more aggressive with higher distillate (diesel-range) products. This was based on an assumption that more favorable reaction chemistry (such as coupling) can be made possible in a separate reactor where, unlike in an in situ upgrading reactor, one does not have to deal with catalyst mixing with biomass char and ash, which pose challenges to catalyst performance and maintenance. Natural gas was used for hydrogen production, but only when off gases from the process was not sufficient to meet the needs; natural gas consumption is insignificant in both the in situ and ex situ base cases. Heat produced from the burning of char, coke, and off-gases allows for the production of surplus electricity which is sold to the grid allowing a reduction of approximately 5¢/GGE in the MFSP.

  7. Mercury vapor hollow cathode component studies. [emissive materials for ion thruster requirements

    Science.gov (United States)

    Zuccaro, D. E.

    1973-01-01

    An experimental study of starting and operating characteristics of conventional hollow cathodes and of hollow cathodes without alkaline earth emissive materials demonstrated that the emissive mix is essential to obtain the desired cathode operation. Loss of the emissive mix by evaporation and chemical reaction was measured. New insert designs consisting of emissive mix supported on nickel and of barium impregnated porous tungsten were studied. Cathodes with a modified orifice geometry operated in a low voltage, 'spot' mode over a broad range of discharge current. Thermal degradation tests on cathode heaters showed the flame sprayed SERT II type to be the most durable at high temperatures. Thermal shock was observed to be a significant factor in limiting cathode heater life. A cathode having a barium impregnated porous tungsten tip and a heater which is potted in sintered alumina was found to have favorable operating characteristics.

  8. Mercury vapor hollow cathode component studies. [emissive materials for ion thruster requirements

    Science.gov (United States)

    Zuccaro, D. E.

    1973-01-01

    An experimental study of starting and operating characteristics of conventional hollow cathodes and of hollow cathodes without alkaline earth emissive materials demonstrated that the emissive mix is essential to obtain the desired cathode operation. Loss of the emissive mix by evaporation and chemical reaction was measured. New insert designs consisting of emissive mix supported on nickel and of barium impregnated porous tungsten were studied. Cathodes with a modified orifice geometry operated in a low voltage, 'spot' mode over a broad range of discharge current. Thermal degradation tests on cathode heaters showed the flame sprayed SERT II type to be the most durable at high temperatures. Thermal shock was observed to be a significant factor in limiting cathode heater life. A cathode having a barium impregnated porous tungsten tip and a heater which is potted in sintered alumina was found to have favorable operating characteristics.

  9. Mercury determination in non- and biodegradable materials by cold vapor capacitively coupled plasma microtorch atomic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Frentiu, Tiberiu, E-mail: ftibi@chem.ubbcluj.ro [Faculty of Chemistry and Chemical Engineering, Babes-Bolyai University, Arany Janos 11, 400028 Cluj-Napoca (Romania); Mihaltan, Alin I., E-mail: alinblaj2005@yahoo.com [National Institute for Research and Development of Optoelectronics Bucharest - Research Institute for Analytical Instrumentation, Donath 67, 400293 Cluj-Napoca (Romania); Ponta, Michaela, E-mail: mponta@chem.ubbcluj.ro [Faculty of Chemistry and Chemical Engineering, Babes-Bolyai University, Arany Janos 11, 400028 Cluj-Napoca (Romania); Darvasi, Eugen, E-mail: edarvasi@chem.ubbcluj.ro [Faculty of Chemistry and Chemical Engineering, Babes-Bolyai University, Arany Janos 11, 400028 Cluj-Napoca (Romania); Frentiu, Maria, E-mail: frentiu.maria@yahoo.com [National Institute for Research and Development of Optoelectronics Bucharest - Research Institute for Analytical Instrumentation, Donath 67, 400293 Cluj-Napoca (Romania); Cordos, Emil, E-mail: emilcordos@gmail.com [National Institute for Research and Development of Optoelectronics Bucharest - Research Institute for Analytical Instrumentation, Donath 67, 400293 Cluj-Napoca (Romania)

    2011-10-15

    Highlights: {yields} Use of a miniaturized analytical system with microtorch plasma for Hg determination. {yields} Determination of Hg in non- and biodegradable materials using cold vapor generation. {yields} Figures of merit and advantages of the miniaturized system for Hg determination. - Abstract: A new analytical system consisting of a low power capacitively coupled plasma microtorch (20 W, 13.56 MHz, 150 ml min{sup -1} Ar) and a microspectrometer was investigated for the Hg determination in non- and biodegradable materials by cold-vapor generation, using SnCl{sub 2} reductant, and atomic emission spectrometry. The investigated miniaturized system was used for Hg determination in recyclable plastics from electronic equipments and biodegradable materials (shopping bags of 98% biodegradable polyethylene and corn starch) with the advantages of easy operation and low analysis costs. Samples were mineralized in HNO{sub 3}-H{sub 2}SO{sub 4} mixture in a high-pressure microwave system. The detection limits of 0.05 ng ml{sup -1} or 0.08 {mu}g g{sup -1} in solid sample were compared with those reported for other analytical systems. The method precision was 1.5-9.4% for Hg levels of 1.37-13.9 mg kg{sup -1}, while recovery in two polyethylene certified reference materials in the range 98.7 {+-} 4.5% (95% confidence level).

  10. Evaluation of vapor generation for the determination of nickel by inductively coupled plasma-atomic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Marrero, Julieta [Comision Nacional de Energia Atomica, Unidad de Actividad Quimica, Centro Atomico Constituyentes, Av. Gral. Paz 1499, 1650-San Martin, Pcia. de Buenos Aires (Argentina); Smichowski, Patricia [Comision Nacional de Energia Atomica, Unidad Proyectos Especiales de Suministros Nucleares, Av. Libertador 8250, 1429-Buenos Aires (Argentina)

    2002-09-01

    Volatile species of Ni were generated by merging acidified aqueous samples and sodium tetrahydroborate(III) in a continuous flow system. The gaseous analyte was subsequently introduced via a stream of Ar carrier into the inlet tube of the plasma torch. Inductively coupled plasma atomic emission spectrometry (ICP-AES) was used for detection. The operating conditions (chemical and physical parameters) and the concentrations of different acids were evaluated for the efficient generation of Ni vapor. The detection limit (3 {sigma}{sub blank}) was 1.8 ng mL{sup -1}. The precision (RSD) of the determination was 4.2% at a level of 500 ng mL{sup -1} and 7.3% for 20 ng mL{sup -1} (n=10). The efficiency of the generation process was estimated to be 51%. The possible interfering effect of transition metals (Cd, Co, Cu, Cr, Fe, Mn, Zn), hydride forming elements (As, Ge, Pb, Sb, Se, Sn, Te), and Hg on Ni signal was examined. This study has demonstrated that Ni vapor generation is markedly free of interferences. (orig.)

  11. Nitric oxide-assisted atmospheric pressure corona discharge ionization for the analysis of automobile hydrocarbon emission species.

    Science.gov (United States)

    Dearth, M A; Komiski, T J

    1994-12-01

    Nitric oxide reagent gas has been found to improve the sensitivity and robustness of the atmospheric pressure corona discharge ionization (APCDI) process. Sensitivity has been increased by a factor of 20-100, depending on the compound, over APCDI without nitric oxide. The robustness (defined as the sensitivity to matrix interferences) of APCDI in the presence of water has been improved by a factor of 3 over normal APCDI. These improvements are due in part to a modification of the commercial inlet system and ionization chamber that allows the chamber and sample gases to be heated to 100 and 350°C, respectively. Nitric oxide was chosen as the reagent gas because of the variety and selectivity of its interaction with hydrocarbons with differing functional groups. Product ions of nitric oxide ionization and their subsequent tandem mass spectra are presented and discussed for selected alkanes; alkenes, alkylbenzenes, alcohols; aldehydes, and an ether. A tandem mass spectrometry (unique parent ion-daughter ion transition) method was developed to quantify compounds of specific interest in vehicle emissions. The absolute sensitivity for these compounds, under ideal conditions, was determined and ranges from 0.006 ppb for xylene (most sensitive) to 80 ppb for C8 (or larger) normal alkanes. Routine sensitivity for real-world samples was in the single parts per billion range for aromatic and olefinic species. Potential applications include the real-time, on-line monitoring of selected hydrocarbons in automobile exhaust.

  12. Polycyclic aromatic hydrocarbon emission profiles and removal efficiency by electrostatic precipitator and wetfine scrubber in an iron ore sintering plant

    Energy Technology Data Exchange (ETDEWEB)

    Ettore Guerriero; Antonina Lutri; Rosanna Mabilia; Maria Concetta Tomasi Sciano; Mauro Rotatori [Istituto sull' Inquinamento Atmosferico, Monterotondo Scalo (Italy). Consiglio Nazionale delle Ricerche

    2008-11-15

    A monitoring campaign of polychlorinated dibenzo-p-dioxins and dibenzofurans, polyaromatic hydrocarbons (PAHs), and polychlorinated biphenyl was carried out in an Italian iron ore sintering plant by sampling the combustion gases at the electrostatic precipitator (ESP) outlet, at the Wetfine scrubber (WS) outlet, and by collecting the ESP dust. Few data are available on these micropollutants produced in iron ore sintering plants, particularly from Italian plants. This study investigates the PAH emission profiles and the removal efficiency of ESPs and WS. PAHs were determined at the stack, ESP outlet flue gases, and in ESP dust to characterize the emission profiles and the performance of the ESP and the WS for reducing PAH emission. The 11 PAHs monitored are listed in the Italian legislative decree 152/2006. The mean total PAH sum concentration in the stack flue gases is 3.96 {mu}g/N m{sup 3}, in ESP outlet flue gases is 9.73 {mu}g/N m{sup 3}, and in ESP dust is 0.53 {mu}g/g. Regarding the emission profiles, the most abundant compound is benzo(b)fluoranthene, which has a relative low BaP toxic equivalency factors (TEF) value, followed by dibenzo(a,l)pyrene, which has a very high BaP(TEF) value. The emission profiles in ESP dust and in the flue gases after the ESP show some changes, whereas the fingerprint in ESP and stack flue gases is very similar. The removal efficiency of the ESP and of WS on the total PAH concentration is 5.2 and 59.5%, respectively. 2 figs., 5 tabs.

  13. Increase in polycyclic aromatic hydrocarbon (PAH) emissions due to briquetting: A challenge to the coal briquetting policy.

    Science.gov (United States)

    Chen, Yingjun; Zhi, Guorui; Feng, Yanli; Chongguo Tian; Bi, Xinhui; Li, Jun; Zhang, Gan

    2015-09-01

    Both China and UNEP recommend replacing raw coal chunks with coal briquettes in household sector as clean coal technology (CCT), which has been confirmed by the decreased emissions of particulate matter and black carbon. However, the clean effect has never been systematically checked by other pollutants like polycyclic aromatic hydrocarbons (PAHs). In this study, 5 coals with different geological maturities were processed as both chunks and briquettes and burned in 3 typical coal stoves for the measurement of emission factors (EFs) of particle-bound PAHs. It was found that the EFs of 16 parent PAHs, 26 nitrated PAHs, 6 oxygenated PAHs, and 8 alkylated PAHs for coal briquettes were 6.90 ± 7.89, 0.04 ± 0.03, 0.65 ± 0.40, and 72.78 ± 18.23 mg/kg, respectively, which were approximately 3.1, 3.7, 1.9, and 171 times those for coal chunks, respectively. Such significant increases in PAH emissions increased human health risk and challenged the policy of CCT. Copyright © 2015 Elsevier Ltd. All rights reserved.

  14. Evaluation of Five Phase Digitally Controlled Rotating Field Plasma Source for Photochemical Mercury Vapor Generation Optical Emission Spectrometry.

    Science.gov (United States)

    Matusiewicz, Henryk; Ślachciński, Mariusz; Pawłowski, Paweł; Portalski, Marek

    2015-01-01

    A new sensitive method for total mercury determination in reference materials using a 5-phase digitally controlled rotating field plasma source (RFP) for optical emission spectrometry (OES) was developed. A novel synergic effect of ultrasonic nebulization (USN) and ultraviolet-visible light (UV-Vis) irradiation when used in combination was exploited for efficient Hg vapor generation. UV- and Vis-based irradiation systems were studied. It was found that the most advantageous design was an ultrasonic nebulizer fitted with a 6 W mercury lamp supplying a microliter sample to a quartz oscillator, converting liquid into aerosol at the entrance of the UV spray chamber. Optimal conditions involved using a 20% v/v solution of acetic acid as the generation medium. The mercury cold vapor, favorably generated from Hg(2+) solutions by UV irradiation, was rapidly transported into a plasma source with rotating field generated within the five electrodes and detected by digitally controlled rotating field plasma optical emission spectrometry (RFP-OES). Under optimal conditions, the experimental concentration detection limit for the determination, calculated as the concentration giving a signal equal to three times the standard deviation of the blank (LOD, 3σblank criterion, peak height), was 4.1 ng mL(-1). The relative standard deviation for samples was equal to or better than 5% for liquid analysis and microsampling capability. The methodology was validated through determination of mercury in three certified reference materials (corresponding to biological and environmental samples) (NRCC DOLT-2, NRCC PACS-1, NIST 2710) using the external aqueous standard calibration techniques in acetic acid media, with satisfactory recoveries. Mercury serves as an example element to validate the capability of this approach. This is a simple, reagent-saving, cost-effective and green analytical method for mercury determination.

  15. CO2 emission free co-generation of energy and ethylene in hydrocarbon SOFC reactors with a dehydrogenation anode.

    Science.gov (United States)

    Fu, Xian-Zhu; Lin, Jie-Yuan; Xu, Shihong; Luo, Jing-Li; Chuang, Karl T; Sanger, Alan R; Krzywicki, Andrzej

    2011-11-21

    A dehydrogenation anode is reported for hydrocarbon proton conducting solid oxide fuel cells (SOFCs). A Cu-Cr(2)O(3) nanocomposite is obtained from CuCrO(2) nanoparticles as an inexpensive, efficient, carbon deposition and sintering tolerant anode catalyst. A SOFC reactor is fabricated using a Cu-Cr(2)O(3) composite as a dehydrogenation anode and a doped barium cerate as a proton conducting electrolyte. The protonic membrane SOFC reactor can selectively convert ethane to valuable ethylene, and electricity is simultaneously generated in the electrochemical oxidative dehydrogenation process. While there are no CO(2) emissions, traces of CO are present in the anode exhaust when the SOFC reactor is operated at over 700 °C. A mechanism is proposed for ethane electro-catalytic dehydrogenation over the Cu-Cr(2)O(3) catalyst. The SOFC reactor also has good stability for co-generation of electricity and ethylene at 700 °C.

  16. Concentrations and emissions of gasoline and other vapors from residential vehicle garages

    Science.gov (United States)

    Batterman, Stuart; Hatzivasilis, Gina; Jia, Chunrong

    High concentrations of airborne volatile organic compounds (VOCs) may be present in residential garages due to emissions from vehicles, lawnmowers, storage containers, and many other items stored in the garage. VOC emissions will ultimately be transported into ambient air and, if the garage is attached to a residence or other building, into living spaces. This study reports on VOC concentrations and emissions at 15 residential garages in Michigan that varied in type, size, use and other characteristics. VOCs were measured in garages and in outside air using 4-day passive sampling, thermal desorption, and GC-MS analysis. Effective air exchange rates (AERs) were determined using a perfluorocarbon tracer gas and the constant injection method. A modeling analysis shows the effect of time-varying ventilation. To estimate temporal and spatial variability, concentrations were measured on 7 subsequent occasions at multiple locations in one garage. This garage was well-mixed, and the temporal variation in AERs and concentrations was modest. Across the 15 garages, 36 different VOCs in garage air, and 20 in ambient air, were quantified. Source groups identified and attributed to garage emissions included evaporated gasoline, solvents, paints, oils, and cleaners. Concentrations of gasoline-related VOCs in most garages were high, e.g., benzene levels reached 159 μg m -3 in one garage. TVOC emissions per garage averaged 3.0±4.1 g day -1, and AERs averaged 0.77±0.51 h -1. VOC concentrations and AERs were not strongly correlated to observed house, garage or meteorological factors, but appeared largely dependent on occupant activities (opening of the garage door) and VOC sources present. This study quantifies the importance of attached garages as VOC sources, and the results are significant for understanding and mitigating indoor exposures, and for estimating emissions for source inventory purposes.

  17. On the accuracy of HITEMP-2010 calculated emissivities of Water Vapor and Carbon Dioxide

    DEFF Research Database (Denmark)

    Alberti, M.; Weber, R.; Mancini, M.

    Nowadays, spectral Line-by-Line calculations using either HITRAN or HITEMP data bases are frequently used for calculating gas radiation properties like absorption coefficients or emissivities. Such calculations are computationally very expensive because of the vast number of spectral lines and...... of spectral transmissivities which were done for H2O-CO2-N2 mixtures for temperatures up to 1770K. Using these measured data it is possible to compare the Line-by-Line calculation using HITEMP-2010 on the basis of total (spectrally averaged) emissivity. At high pressures, also a proper lineshape treatment...

  18. PROBLEMS WITH DETERMINATION OF FUGITIVE EMISSION OF POLYCYCLIC AROMATIC HYDROCARBONS FROM COKE OVEN BATTERY

    Directory of Open Access Journals (Sweden)

    Rafał Bigda

    2017-03-01

    Full Text Available Coke oven battery is complex and multifaceted facility in terms of air pollutant emissions. As far as stack or quenching tower does not cause major difficulties of emission measurement, the fugitive emission measurement from sources such as battery top elements (charging holes, ascension pipes or oven doors is still complicated and not fully solved problem. This article presents the discussion concerning main problems and errors likely to be made in particular stages of procedure of fugitive emissions characterization from coke oven battery (selection of sampling points, sampling itself, measurement of air velocity over battery top and laboratory analyses. In addition, results of concentrations measurements of selected substances characteristic for the coking process (naphthalene, anthracene, 4 PAHs and TSP originating from fugitive sources of coke oven battery and subjected to reporting under the E-PRTR are presented. The measurements were carried out on coke oven battery top in points selected on the basis of the preceding detailed air convection velocity measurements over battery top. Results of the velocity measurements were compared with results of numerical modelling using CFD software. The presented material is an attempt to cross-sectional presentation of issues related to the quantitative evaluation of fugitive emission from coke oven battery, discussed on the example of PAHs emission as a group of substances characteristic for coking of coal.

  19. On the accuracy of HITEMP-2010 calculated emissivities of Water Vapor and Carbon Dioxide

    DEFF Research Database (Denmark)

    Alberti, Michael; Weber, Roman; Mancini, Marco

    2015-01-01

    Line-by-line (LbL) calculations using either HITRAN or HITEMP spectral data bases are often used for predicting gas radiation properties like absorption coefficients or emissivities. Due to the large size of these data bases, calculations are computationally too expensive to be used in regular CFD...

  20. Geographic variations in female breast cancer incidence in relation to ambient air emissions of polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Large, Courtney; Wei, Yudan

    2017-07-01

    A significant geographic variation of breast cancer incidence exists, with incidence rates being much higher in industrialized regions. The objective of the current study was to assess the role of environmental factors such as exposure to ambient air pollution, specifically carcinogenic polycyclic aromatic hydrocarbons (PAHs) that may be playing in the geographic variations in breast cancer incidence. Female breast cancer incidence and ambient air emissions of PAHs were examined in the northeastern and southeastern regions of the USA by analyzing data from the Surveillance, Epidemiology, and End Results (SEER) Program and the State Cancer Profiles of the National Cancer Institute and from the Environmental Protection Agency. Linear regression analysis was conducted to evaluate the association between PAH emissions and breast cancer incidence in unadjusted and adjusted models. Significantly higher age-adjusted incidence rates of female breast cancer were seen in northeastern SEER regions, when compared to southeastern regions, during the years of 2000-2012. After adjusting for potential confounders, emission densities of total PAHs and four carcinogenic individual PAHs (benzo[a]pyrene, dibenz[a,h]anthracene, naphthalene, and benzo[b]fluoranthene) showed a significantly positive association with annual incidence rates of breast cancer, with a β of 0.85 (p = 0.004), 58.37 (p = 0.010), 628.56 (p = 0.002), 0.44 (p = 0.041), and 77.68 (p = 0.002), respectively, among the northeastern and southeastern states. This study suggests a potential relationship between ambient air emissions of carcinogenic PAHs and geographic variations of female breast cancer incidence in the northeastern and southeastern US. Further investigations are needed to explore these interactions and elucidate the role of PAHs in regional variations of breast cancer incidence.

  1. Measuring Star-Formation Rates of AGNs and QSOs using a new calibration from Polycyclic Aromatic Hydrocarbon Emission

    Science.gov (United States)

    Papovich, Casey

    Understanding the coevolution of star-formation and supermassive black hole accretion is one of the key questions in galaxy formation theory. This relation is important for understanding why at present the mass in galaxy bulges (on scales of kpc) correlates so tightly with the mass of galaxy central supermassive blackholes (on scales of AU). Feedback from supermassive black hole accretion may also be responsible for heating or expelling cold gas from galaxies, shutting off the fuel for star-formation and additional black hole growth. Did bulges proceed the formation of black holes, or vice versa, or are they contemporaneous? Therefore, understanding the exact rates of star-formation and supermassive black hole growth, and how they evolve with time and galaxy mass has deep implications for how galaxies form. It has previously been nearly impossible to study simultaneously both star-formation and accretion onto supermassive black holes in galaxies because the emission from black hole accretion contaminates nearly all diagnostics of star-formation. The "standard" diagnostics for the star-formation rate (the emission from hydrogen, UV emission, midIR emission, far-IR emission, etc) are not suitable for measuring star-formation rates in galaxies with actively accreting supermassive blackholes. In this proposal, the researchers request NASA/ADP funding for an archival study using spectroscopy with the Spitzer Space Telescope to measure simultaneously the star-formation rate (SFR) and bolometric emission from accreting supermassive blackholes to understand the complex relation between both processes. The key to this study is that they will develop a new calibrator for SFRs in galaxies with active supermassive black holes based on the molecular emission from polycyclic aromatic hydrocarbons (PAHs), which emit strongly in the mid-IR (3 - 20 micron) and are very strong in spectra from the Spitzer Space Telescope. The PAH molecules exist near photo-dissociation regions, and

  2. Nine years of global hydrocarbon emissions based on source inversion of OMI formaldehyde observations

    Science.gov (United States)

    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

    As formaldehyde (HCHO) is a high-yield product in the oxidation of most volatile organic compounds (VOCs) emitted by fires, vegetation, and anthropogenic activities, satellite observations of HCHO are well-suited to inform us on the spatial and temporal variability of the underlying VOC sources. The long record of space-based HCHO column observations from the Ozone Monitoring Instrument (OMI) is used to infer emission flux estimates from pyrogenic and biogenic volatile organic compounds (VOCs) on the global scale over 2005-2013. This is realized through the method of source inverse modeling, which consists in the optimization of emissions in a chemistry-transport model (CTM) in order to minimize the discrepancy between the observed and modeled HCHO columns. The top-down fluxes are derived in the global CTM IMAGESv2 by an iterative minimization algorithm based on the full adjoint of IMAGESv2, starting from a priori emission estimates provided by the newly released GFED4s (Global Fire Emission Database, version 4s) inventory for fires, and by the MEGAN-MOHYCAN inventory for isoprene emissions. The top-down fluxes are compared to two independent inventories for fire (GFAS and FINNv1.5) and isoprene emissions (MEGAN-MACC and GUESS-ES). The inversion indicates a moderate decrease (ca. 20 %) in the average annual global fire and isoprene emissions, from 2028 Tg C in the a priori to 1653 Tg C for burned biomass, and from 343 to 272 Tg for isoprene fluxes. Those estimates are acknowledged to depend on the accuracy of formaldehyde data, as well as on the assumed fire emission factors and the oxidation mechanisms leading to HCHO production. Strongly decreased top-down fire fluxes (30-50 %) are inferred in the peak fire season in Africa and during years with strong a priori fluxes associated with forest fires in Amazonia (in 2005, 2007, and 2010), bushfires in Australia (in 2006 and 2011), and peat burning in Indonesia (in 2006 and 2009), whereas generally increased fluxes

  3. Field-Emission Study of Multi-Walled Carbon Nanotubes Grown On Si Substrate by Low Pressure Chemical Vapor Deposition

    Directory of Open Access Journals (Sweden)

    J. Ali

    2011-01-01

    Full Text Available CNTs are synthesized by Low Pressure Chemical Vapor Deposition (LPCVD method at 600 °C. The Si substrate is coated with Fe, used as a catalyst, by RF- sputtering. The thickness of the catalyst film is measured to be approximately 15 nm. Three precursor gases Acetylene (C2H2, Ammonia (NH3 and Hydrogen (H2 with flow rates 15 sccm, 100 sccm and 100 sccm respectively are allowed to flow through the tube reactor for 20 minutes. The as grown CNTs sample was characterized by Scanning Electron Microscope (SEM. SEM images show that the diameter of as grown CNTs is in the range of 20-50 nm. Field emission properties of as grown sample have also been studied. The CNTs film shows good field emission with turn on field Eα = 2.10 V/μm at the current density of 4.59 mA/cm2 with enhancement factor β = 1.37 × 102.

  4. A Survey of 557 GHz Water Vapor Emission in the NGC 1333 Molecular Cloud

    CERN Document Server

    Bergin, E A; Melnick, G J; Snell, R L; Howe, J E; Bergin, Edwin A.; Kaufman, Michael J.; Melnick, Gary J.; Snell, Ronald L.; Howe, John E.

    2003-01-01

    Using NASA's Submillimeter Wave Astronomy Satellite (SWAS) we have examined the production of water in quiescent and shocked molecular gas through a survey of the 556.936 GHz transition of ortho-H2O in the NGC 1333 molecular core. These observations reveal broad emission lines associated with the IRAS~2, IRAS~4, IRAS~7, and HH7-11 outflows. Towards 3 positions we detect narrow (~2-3 km/s) emission lines clearly associated with the ambient gas. The SWAS observations, with a resolution of 4', are supplemented with observations from the Infrared Space Observatory (ISO) and by an unbiased survey of a 17' x 15' area, with 50" resolution, in the low-J transitions of CO, 13CO, C18O, N2H+, CH3OH, and SiO. Using these combined data sets, with consistent assumptions, we find beam-averaged o-H2O abundances of > 10^{-6} relative to H2O for all four outflows. A comparison of SWAS and ISO water data is consistent with non-dissociative shock models, provided the majority of the 557 GHz emission arises from cool post-shock m...

  5. Influence of fuel composition on polycyclic aromatic hydrocarbon emissions from a fleet of in-service passenger cars

    Science.gov (United States)

    Lim, McKenzie C. H.; Ayoko, Godwin A.; Morawska, Lidia.; Ristovski, Zoran D.; Jayaratne, E. Rohan

    The composition of exhaust emissions from eight in-service passenger cars powered by liquefied petroleum gas (LPG) and unleaded petrol (ULP) were measured on a chassis dynamometer at two driving speeds (60 and 80 km h -1) with the aims of evaluating their polycyclic aromatic hydrocarbon (PAH) contents and investigating the effects of the type of fuel on vehicle performance, ambient air quality and associated health risks. Naphthalene, fluorene, phenanthrene, anthracene, pyrene, chrysene, benzo(a)anthracene and benzo(b)fluoranthene were the most prominent PAHs emitted by both ULP and LPG powered cars. The total emission factors of PAHs from LPG cars were generally lower than (but statistically comparable with) those of ULP cars. Similarly, the total BAP eq of the PAHs emitted by LPG cars were lower than those from ULP cars. Multi-criteria decision making (MCDM) methods showed that cars powered by LPG fuel performed better than those powered by ULP fuel in term of PAH levels. The implications of these observations on the advantages and disadvantages of using ULP and LPG fuels are discussed.

  6. Probing the Ionization States of Polycyclic Aromatic Hydrocarbons via the 15-20 {\\mu}m Emission Bands

    CERN Document Server

    Shannon, M J; Peeters, E

    2015-01-01

    We report new correlations between ratios of band intensities of the 15-20 {\\mu}m emission bands of polycyclic aromatic hydrocarbons (PAHs) in a sample of fifty-seven sources observed with Spitzer/IRS. This sample includes Large Magellanic Cloud point sources from the SAGE-Spec survey, nearby galaxies from the SINGS survey, two Galactic ISM cirrus sources and the spectral maps of the Galactic reflection nebulae NGC 2023 and NGC 7023. We find that the 16.4, 17.4 and 17.8 {\\mu}m band intensities are inter-correlated in all environments. In NGC 2023 and NGC 7023 these bands also correlate with the 11.0 and 12.7 {\\mu}m band intensities. The 15.8 {\\mu}m band correlates only with the 15-20 {\\mu}m plateau and the 11.2 {\\mu}m emission. We examine the spatial morphology of these bands and introduce radial cuts. We find that these bands can be spatially organized into three sets: the 12.7, 16.4 and 17.8 {\\mu}m bands; the 11.2, 15.8 {\\mu}m bands and the 15-18 {\\mu}m plateau; and the 11.0 and 17.4 {\\mu}m bands. We also f...

  7. Estimating emissions of toxic hydrocarbons from natural gas production sites in the Barnett Shale region

    Science.gov (United States)

    Marrero, J. E.; Townsend-Small, A.; Lyon, D. R.; Tsai, T.; Meinardi, S.; Blake, D. R.

    2015-12-01

    Throughout the past decade, shale gas operations have moved closer to urban centers and densely populated areas, contributing to growing public concerns regarding exposure to hazardous air pollutants (HAPs). These HAPs include gases like hexane, 1,3-butadiene and BTEX compounds, which can cause minor health effects from short-term exposure or possibly cancer due to prolonged exposure. During the Barnett Shale Coordinated Campaign in October, 2013, ground-based whole air samples revealed enhancements in several of these toxic volatile organic compounds (VOCs) downwind of natural gas well pads and compressor stations. Two methods were used to estimate the emission rate of several HAPs in the Barnett Shale. The first method utilized CH4 flux measurements derived from the Picarro Mobile Flux Plane (MFP) and taken concurrently with whole air samples, while the second used a CH4 emissions inventory developed for the Barnett Shale region. From these two approaches, the regional emission estimate for benzene (C6H6) ranged from 48 ± 16 to 84 ± 26 kg C6H6 hr-1. A significant regional source of atmospheric benzene is evident, despite measurement uncertainty and limited number of samples. The extent to which these emission rates equate to a larger public health risk is unclear, but is of particular interest as natural gas productions continues to expand.

  8. Theoretical modeling of infrared emission from neutral and charged polycyclic aromatic hydrocarbons. I.

    NARCIS (Netherlands)

    Bakes, ELO; Tielens, AGGM; Bauschlicher, CW

    2001-01-01

    Since the discovery of interstellar infrared emission features in the 3.3-12.7 mum wavelength range three decades ago, the carriers of these features have been the subject of much debate. Recent observational work with the Infrared Space Observatory, experimental work, and quantum chemical calculati

  9. Polycyclic Aromatic Hydrocarbon emission in Spitzer/IRS maps I: Catalog and simple diagnostics

    CERN Document Server

    Stock, D J; Moya, L G V; Otaguro, J N; Sorkhou, S; Allamandola, L J; Tielens, A G G M; Peeters, E

    2016-01-01

    We present a sample of resolved galactic HII regions and photodissociation regions (PDRs) observed with the Spitzer infrared spectrograph (IRS) in spectral mapping mode between the wavelengths of 5--15 $\\mu$m. For each object we have spectral maps at a spatial resolution of $\\sim$4" in which we have measured all of the mid-infrared emission and absorption features. These include the PAH emission bands, primarily at 6.2, 7.7, 8.6, 11.2 and 12.7 $\\mu$m, as well as the spectral emission lines of neon and sulfur and the absorption band caused by silicate dust at around 9.8 $\\mu$m. In this work we describe the data in detail, including the data reduction and measurement strategies, and subsequently present the PAH emission band intensity correlations for each of the objects and the sample as a whole. We find that there are distinct differences between the sources in the sample, with two main groups, the first comprising the HII regions and the second the reflection nebulae (RNe). Three sources, the reflection nebu...

  10. Decreasing polycyclic aromatic hydrocarbons emission from bitumen using alternative bitumen production process.

    Science.gov (United States)

    Rasoulzadeh, Y; Mortazavi, S B; Yousefi, A A; Khavanin, A

    2011-01-30

    In 1988, the National Institute for Occupational Safety and Health (NIOSH) recommended that bitumen fumes should also be considered a potential occupational carcinogen and management practices such as engineering controls should be implemented. Changing the production process of bitumen, as a source control method, was investigated in our study. For the first time, a novel alternative process was used to produce paving grade bitumen with decreased PAH emissions as well as improved bitumen performance grade (PG). Post-consumer latex and natural bitumen (NB) were used as additives to obtain 60/70 modified bitumen directly from the vacuum bottom (VB) without any need for air-blowing. The emissions were produced by a laboratory fume generation rig and were sampled and analyzed by GC-Mass and GC-FID as described in NIOSH method 5515. The PG of the resulting modified 60/70 bitumen in this study covers a wider range of climatic conditions and has higher total resistance against deformation than conventional 60/70 bitumen. The total PAH emissions from modified 60/70 bitumen (100.2619 ng/g) were decreased approximately to 50% of PAHs emitted from conventional 60/70 bitumen (197.696 ng/g). Therefore, it is possible to obtain modified bitumen with lower PAH emissions and better quality than conventional bitumen via additives and without air-blowing.

  11. Polycyclic aromatic hydrocarbon and particulate emissions from two-stage combustion of polystyrene: the effect of the primary furnace temperature.

    Science.gov (United States)

    Wang, J; Levendis, Y A; Richter, H; Howard, J B; Carlson, J

    2001-09-01

    A study is presented on laboratory-scale combustion of polystyrene (PS) to identify staged-combustion conditions that minimize emissions. Batch combustion of shredded PS was conducted in fixed beds placed in a bench-scale electrically heated horizontal muffle furnace. In most cases, combustion of the samples occurred by forming gaseous diffusion flames in atmospheric pressure air. The combustion effluent was mixed with additional air, and it was channeled to a second muffle furnace (afterburner) placed in series. Further reactions took place in the secondary furnace at a residence time of 0.7 s. The gas temperature of the primary furnace was varied in the range of 500-1,000 degrees C, while that of the secondary furnace was kept fixed at 1,000 degrees C. Sampling for CO, CO2, O2, soot, and unburned hydrocarbon emissions (volatile and semivolatile, by GC-MS) was performed at the exits of the two furnaces. Results showed that the temperature of the primary furnace, where PS gasifies, is of paramount importance to the formation and subsequent emissions of organic species and soot. Atthe lowesttemperatures explored, mostly styrene oligomers were identified at the outlet of the primary furnace, but they did not survive the treatment in the secondary furnace. The formation and emission of polycyclic aromatic hydrocarbons (PAH) and soot were suppressed. As the temperature in the first furnace was raised, increasing amounts of a wide range of both unsubstituted and substituted PAH containing up to at least seven condensed aromatic rings were detected. A similar trend was observed for total particulate yields. The secondary furnace treatment reduced the yields of total PAH, but it had an ambiguous effect on individual species. While most low molecular mass PAH were reduced in the secondary furnace, concentrations of some larger PAH increased under certain conditions. Thus, care in the selection of operating conditions of both the primary furnace (gasifier/ burner) and the

  12. Atmospheric Longwave Infrared Emission Spectroscopy of Water Vapor at the South Pole

    OpenAIRE

    Myers, Brooke A.

    2000-01-01

    The downward infrared radiance spectrum was measured with a Michelson Long Wave Infrared (LWIR) spectrometer at the Amundsen-Scott South Pole Station. Spectra were collected year-round at the South Pole in 1998. This research focuses on the atmospheric water emission lines between 250 and 800 cm-1 (40 to 12.5 μm) region. The spectral resolution is 1 cm-1. The atmosphere over the South Pole is the driest and coldest on Earth. Winter surface temperatures average approximately -60°C, while the t...

  13. Implications of changing urban and rural emissions on non-methane hydrocarbons in the Pearl River Delta region of China

    Science.gov (United States)

    Tang, J. H.; Chan, L. Y.; Chan, C. Y.; Li, Y. S.; Chang, C. C.; Wang, X. M.; Zou, S. C.; Barletta, Barbara; Blake, D. R.; Wu, Dui

    2008-05-01

    Guangzhou (GZ) is one of the highly industrialized and economically vibrant cities in China, yet it remains relatively understudied in terms of its air quality, which has become severely degraded. In this study, extensive air sampling campaigns had been conducted at GZ urban sites and in Dinghu Mountain (DM), a rural site, in the Pearl River Delta (PRD) during the spring of 2001 and 2005. Additionally, roadside and tunnel samples were collected in GZ in 2000 and 2005. Later, exhaust samples from liquefied petroleum gas (LPG)- and gasoline-fueled taxis were collected in 2006. All samples were analyzed for C2-C10 non-methane hydrocarbons (NMHCs). NMHC profiles showed significant differences in the exhaust samples between gasoline- and LPG-fueled taxis. Propane (47%) was the dominant hydrocarbon in the exhaust of the LPG-fueled taxis, while ethene (35%) was the dominant one in that of gasoline-fueled taxis. The use of LPG-fueled buses and taxis since 2003 and the leakage from these LPG-fueled vehicles were the major factors for the much higher level of propane in GZ urban area in 2005 compared to 2001. The mixing ratios of toluene, ethylbenzene, m/p-xylene and o-xylene decreased at the GZ and DM sites between 2001 and 2005, especially for toluene in GZ, despite the sharp increase in the number of registered motor vehicles in GZ. This phenomenon was driven in part by the closure of polluting industries as well as the upgrading of the road network in urban GZ and in part by the implementation of more stringent emission standards for polluting industries and motor vehicles in the PRD region.

  14. 40 CFR 63.649 - Alternative means of emission limitation: Connectors in gas/vapor service and light liquid service.

    Science.gov (United States)

    2010-07-01

    ... limitation: Connectors in gas/vapor service and light liquid service. 63.649 Section 63.649 Protection of...: Connectors in gas/vapor service and light liquid service. (a) If an owner or operator elects to monitor... gas/vapor service and for connectors in light liquid service. The data for the two groups...

  15. Generation rates and emission factors of particulate matter and particle-bound polycyclic aromatic hydrocarbons of incense sticks.

    Science.gov (United States)

    Lung, Shih-Chun Candice; Hu, Shu-Chuan

    2003-02-01

    The generation rates and emission factors of particulate matter and associated polycyclic aromatic hydrocarbons (PAHs) from incense burning were assessed in a laboratory setting. The differences among different segments of the same stick, among different sticks of the same kind of incense, and between two kinds of manually made Chih-Chen incense sticks (A and B) were evaluated. Joss sticks were burned inside a 44 cm long elutriator; personal environmental monitors fitted into the top of the elutriator were used to take PM2.5 and PM10 samples of incense smoke. Samples were analyzed for PAHs by gas chromatography-flame ionization Detector. It was found that particle and associated PAHs were generated approximately at 561 microg/min (geometric standard deviation (GSD) = 1.1) and 0.56 microg/min (GSD = 1.1) from Incense A, and at 661 microg/min (GSD = 1.7) and 0.46 microg/min (GSD = 1.3) from Incense B, respectively. One gram of Incense A emitted about 19.8 mg (GSD = 1.1) particulate matter and 17.1 microg (GSD = 1.2) particulate-phase PAHs, while one gram of Incense B produced around 43.6 mg (GSD = 1.1) of particles and 25.2 microg (GSD = 1.2) of particle-bound PAHs. There were significant differences in emissions between Incenses A and B, although they belong to the same class of incense. A 10-20% variability in emissions was observed in the main part of the manually produced stick, and a larger variation was found at both tips of the combustible part.

  16. Characteristics of hopanoid hydrocarbons in ambient PM₁₀ and motor vehicle emissions and coal ash in Taiyuan, China.

    Science.gov (United States)

    Han, Feng; Cao, Junji; Peng, Lin; Bai, Huiling; Hu, Dongmei; Mu, Ling; Liu, Xiaofeng

    2015-10-01

    Hopanoid hydrocarbon content in ambient particulate matter (PM) of less than or equal to 10 μm aerodynamic diameter (PM10) was sampled at seven sites representative of different functional districts, and measured by gas chromatography-mass spectrometry. 17α(H),21β(H)-hopane (C30αβ) and 17α(H),21β(H)-30-norhopane (C29αβ) were dominant in all samples. Hopanes in motor vehicle emissions from various fuel-type engines (gasoline, diesel and natural gas) and coal ash were qualitatively measured, and the amount of C30αβ was about two to three times greater than that of C29αβ. Distinct seasonal variations (winter/summer differences) were observed at higher concentrations (45.54-108.29 ng/m(3)) of total hopanes in winter and lower (2.59-28.26 ng/m(3)) in summer. There were also clear spatial variations of hopanes in Taiyuan, with samples with greater hopane concentrations in downtown areas, but less in summer. The spatial distribution reversed in winter. Distributions and relative abundances of selected hopanes from PM10 and source emissions indicated that in summer, vehicle exhaust was the dominant fossil fuel combustion source (C30αβ was >C29αβ), and that the contribution of coal combustion was slightly greater at suburban sites. However, the contribution of coal combustion sources increased significantly at all sites in winter, especially in suburban areas, where C29αβ exceeded C30αβ. Hopanoid indexes revealed a classification of vehicle exhaust and coal combustion emissions in PM10. The results imply that during rapid urbanization, it is crucial to strengthen the construction of infrastructure such as central heating in new city districts and to increase the use of natural gas instead of residential coal burning.

  17. Emissions of Polycyclic Aromatic Hydrocarbons from Natural Gas Extraction into Air.

    Science.gov (United States)

    Paulik, L Blair; Donald, Carey E; Smith, Brian W; Tidwell, Lane G; Hobbie, Kevin A; Kincl, Laurel; Haynes, Erin N; Anderson, Kim A

    2016-07-19

    Natural gas extraction, often referred to as "fracking", has increased rapidly in the United States in recent years. To address potential health impacts, passive air samplers were deployed in a rural community heavily affected by the natural gas boom. Samplers were analyzed for 62 polycyclic aromatic hydrocarbons (PAHs). Results were grouped based on distance from each sampler to the nearest active well. Levels of benzo[a]pyrene, phenanthrene, and carcinogenic potency of PAH mixtures were highest when samplers were closest to active wells. PAH levels closest to natural gas activity were comparable to levels previously reported in rural areas in winter. Sourcing ratios indicated that PAHs were predominantly petrogenic, suggesting that PAH levels were influenced by direct releases from the earth. Quantitative human health risk assessment estimated the excess lifetime cancer risks associated with exposure to the measured PAHs. At sites closest to active wells, the risk estimated for maximum residential exposure was 0.04 in a million, which is below the U.S. Environmental Protection Agency's acceptable risk level. Overall, risk estimates decreased 30% when comparing results from samplers closest to active wells to those farthest from them. This work suggests that natural gas extraction is contributing PAHs to the air, at levels that would not be expected to increase cancer risk.

  18. SPATIALLY RESOLVED l-C{sub 3}H{sup +} EMISSION IN THE HORSEHEAD PHOTODISSOCIATION REGION: FURTHER EVIDENCE FOR A TOP-DOWN HYDROCARBON CHEMISTRY

    Energy Technology Data Exchange (ETDEWEB)

    Guzmán, V. V.; Öberg, K. I. [Harvard-Smithsonian Center for Astrophysics, 60 Garden Street, Cambridge, MA 02138 (United States); Pety, J. [Institut de Radioastronomie Millimétrique (IRAM), 300 rue de la Piscine, F-38406 Saint Martin d’Hères (France); Goicoechea, J. R. [Instituto de Ciencia de Materiales de Madrid (CSIC), E-28049 Cantoblanco, Madrid (Spain); Gerin, M. [LERMA, Observatoire de Paris, École Normale Supérieure, PSL Research University, CNRS, UMR8112, F-75014 Paris (France); Roueff, E. [Sorbonne Universités, UPMC Univ. Paris 06, UMR8112, LERMA, F-75005 Paris (France); Gratier, P., E-mail: vguzman@cfa.harvard.edu [Université de Bordeaux, LAB, UMR 5804, F-33270, Floirac (France)

    2015-02-20

    Small hydrocarbons, such as C{sub 2}H, C{sub 3}H, and C{sub 3}H{sub 2} are more abundant in photo-dissociation regions (PDRs) than expected based on gas-phase chemical models. To explore the hydrocarbon chemistry further, we observed a key intermediate species, the hydrocarbon ion l-C{sub 3}H{sup +}, in the Horsehead PDR with the Plateau de Bure Interferometer at high-angular resolution (6″). We compare with previous observations of C{sub 2}H and c-C{sub 3}H{sub 2} at similar angular resolution and new gas-phase chemical model predictions to constrain the dominant formation mechanisms of small hydrocarbons in low-UV flux PDRs. We find that at the peak of the HCO emission (PDR position), the measured l-C{sub 3}H{sup +}, C{sub 2}H, and c-C{sub 3}H{sub 2} abundances are consistent with current gas-phase model predictions. However, in the first PDR layers, at the 7.7 μm polycyclic aromatic hydrocarbon band emission peak, which are more exposed to the radiation field and where the density is lower, the C{sub 2}H and c-C{sub 3}H{sub 2} abundances are underestimated by an order of magnitude. At this position, the l-C{sub 3}H{sup +} abundance is also underpredicted by the model but only by a factor of a few. In addition, contrary to the model predictions, l-C{sub 3}H{sup +} peaks further out in the PDR than the other hydrocarbons, C{sub 2}H and c-C{sub 3}H{sub 2}. This cannot be explained by an excitation effect. Current gas-phase photochemical models thus cannot explain the observed abundances of hydrocarbons, in particular, in the first PDR layers. Our observations are consistent with a top-down hydrocarbon chemistry, in which large polyatomic molecules or small carbonaceous grains are photo-destroyed into smaller hydrocarbon molecules/precursors.

  19. Nucleation and Oriented Textured Growth of Diamond Films on Si(100) via Electron Emission in Ho.t Filament Chemical Vapor Deposition

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Oriented textured diamond films were obtained on Si(100) substrate via electron emission in hot filament chemical vapor deposition (HFCVD). A dc bias voltage relative to the filament was applied to the tungsten electrode between the substrate and the filament. The nucleation and subsequent growth of diamond films were characterized by scanning electron microscopy and Raman spectroscopy. The experimental results showed that the electron emission from the diamond coating on the electrode played a critical role during the nucleation.The maximum value of nucleation density was up to 1011 cm-2 on pristine Si surface at emission current of 250 mA. The effect of the electron emission on the reactive gas composition was analyzed by in situ infrared absorption, indicating that the concentration of CH3 and C2H2 near the substrate surface was extremely increased. This may be responsible for the enhanced nucleation by electron emission.

  20. Emissions of volatile hydrocarbons (VOC) during drying of sawdust; Utslaepp av laettflyktiga kolvaeten vid torkning av biobraenslen

    Energy Technology Data Exchange (ETDEWEB)

    Granstroem, Karin

    2001-08-01

    In the project 'Emissions of volatile hydrocarbons (VOC) during drying of sawdust' the identity, amount and composition of monoterpenes found in the drying medium of a fluidized bed drier drying sawdust from Norwegian spruce and Scotch pine has been determined. The energy efficiency of the drier has also been measured. The aim of this project was to reduce both emissions and energy required for drying, to minimize environmental and health hazards, and make drying more competitive. This would help our primary target group - small scale saw mills - to make use of the sawdust produced as a by- product by making pellets and briquettes. If the VOC remains in the sawdust its energy content will improve and therefore also its value as a fuel. The sawdust was dried to different moisture levels in a spouted bed drier at atmospheric pressure, using either recirculating or not recirculating drying medium with temperatures 140, 170 or 200 deg C. The emissions of VOC were measured using a flame ionization detector (FID) and the nature of the emissions analyzed with a gas chromatograph with mass spectrometric detector (GC-MS). The GC-MS data is reported as emitted substance per oven dry weight (odw). Experiments show that terpenes do not leave the sawdust in great amounts until it is dried to a moisture content (water/total weight) below 10%. When sawdust is dried to a predetermined moisture level, the terpene emissions increase when warmer incoming drying medium is used. The monoterpenes found in greatest amount are a-pinene, b-pinene, 3-carene, limonene and myrcene. y-terpinene was detected in emissions from pine but not from spruce. The relative amounts of different monoterpenes did not vary significantly with post-drying moisture content, but drying medium of higher temperature caused an increase in the relative amount of less volatile monoterpenes. The FID data is reported as concentration of VOC in the drying medium, and as weight VOC per odw. The concentration

  1. Mercury determination in non- and biodegradable materials by cold vapor capacitively coupled plasma microtorch atomic emission spectrometry.

    Science.gov (United States)

    Frentiu, Tiberiu; Mihaltan, Alin I; Ponta, Michaela; Darvasi, Eugen; Frentiu, Maria; Cordos, Emil

    2011-10-15

    A new analytical system consisting of a low power capacitively coupled plasma microtorch (20 W, 13.56 MHz, 150 ml min(-1) Ar) and a microspectrometer was investigated for the Hg determination in non- and biodegradable materials by cold-vapor generation, using SnCl(2) reductant, and atomic emission spectrometry. The investigated miniaturized system was used for Hg determination in recyclable plastics from electronic equipments and biodegradable materials (shopping bags of 98% biodegradable polyethylene and corn starch) with the advantages of easy operation and low analysis costs. Samples were mineralized in HNO(3)-H(2)SO(4) mixture in a high-pressure microwave system. The detection limits of 0.05 ng ml(-1) or 0.08 μg g(-1) in solid sample were compared with those reported for other analytical systems. The method precision was 1.5-9.4% for Hg levels of 1.37-13.9 mg kg(-1), while recovery in two polyethylene certified reference materials in the range 98.7 ± 4.5% (95% confidence level).

  2. Solid-Sampling Electrothermal Vaporization Inductively Coupled Plasma Optical Emission Spectrometry for Direct Determination of Total Oxygen in Coal.

    Science.gov (United States)

    Vogt, Thomas; Bauer, Daniela; Nennstiel, David; Otto, Matthias

    2015-10-20

    A new analytical method for direct determination of total oxygen contents in eight coal samples of the Argonne Premium Coal (APC) series and in the NIST SRM 1632d is presented. The development of a suitable calibration procedure, optimization of measurement conditions, and the application of a tailored data processing for handling of plasma effects and high blanks enable the quantification of oxygen simultaneously with other trace, minor, or major elements in whole coal samples by means of electrothermal vaporization inductively coupled plasma optical emission spectrometry (ETV-ICP OES). For comparison, the oxygen contents were determined by a direct oxygen analyzer. The obtained oxygen values of the APC and the reference material NIST SRM 1632d were compared to data in the literature. The precision of the ETV-ICP OES was within ±3.5%, and the recovery better than 92%. With this good accuracy, the developed direct solid sampling method ETV-ICP OES is well suited for the fast determination of oxygen in coals, varying in rank from lignite to semianthracite, in a content range of about 100 ppm up to 27% using 1.5 mg sample weight. This direct analysis method represents an accurate, advantageous alternative to currently used methods for estimation of total oxygen contents in coals.

  3. Characterization of low temperature graphene synthesis in inductively coupled plasma chemical vapor deposition process with optical emission spectroscopy.

    Science.gov (United States)

    Ma, Yifei; Kim, Daekyoung; Jang, Haegyu; Cho, Sung Min; Chae, Heeyeop

    2014-12-01

    Low-temperature graphene was synthesized at 400 degrees C with inductively coupled plasma chemical vapor deposition (PECVD) process. The effects of plasma power and flow rate of various carbon containing precursors and hydrogen on graphene properties were investigated with optical emission spectroscopy (OES). Various radicals monitored by OES were correlated with graphene film properties such as sheet resistance, I(D)/I(G) ratio of Raman spectra and transparency. C2H2 was used as a main precursor and the increase of plasma power enhanced intensity of carbon (C2) radical OES intensity in plasma, reduced sheet resistance and increased transparency of graphene films. The reduced flow rate of C2H2 decreased sheet resistance and increased transparency of graphene films in the range of this study. H2 addition was found to increase sheet resistance, transparency and attributed to reduction of graphene grain and etching graphene layers. OES analysis showed that C2 radicals contribute to graphite networking and sheet resistance reduction. TEM and AFM were applied to provide credible information that graphene had been successfully grown at low temperature.

  4. Gasoline Vapor Recovery

    Science.gov (United States)

    1979-01-01

    Gasoline is volatile and some of it evaporates during storage, giving off hydrocarbon vapor. Formerly, the vapor was vented into the atmosphere but anti-pollution regulations have precluded that practice in many localities, so oil companies and storage terminals are installing systems to recover hydrocarbon vapor. Recovery provides an energy conservation bonus in that most of the vapor can be reconverted to gasoline. Two such recovery systems are shown in the accompanying photographs (mid-photo at right and in the foreground below). They are actually two models of the same system, although.configured differently because they are customized to users' needs. They were developed and are being manufactured by Edwards Engineering Corporation, Pompton Plains, New Jersey. NASA technological information proved useful in development of the equipment.

  5. Influence of oil and gas emissions on ambient atmospheric non-methane hydrocarbons in residential areas of Northeastern Colorado

    Directory of Open Access Journals (Sweden)

    Chelsea R. Thompson

    2014-11-01

    Full Text Available Abstract The Northern Front Range (NFR region of Colorado has experienced rapid expansion of oil and gas extraction from shale and tight sands reservoirs in recent years due to advances in hydraulic fracturing technology, with over 25,000 wells currently in operation. This region has also been designated as a federal ozone non-attainment area by the U.S. EPA. High ozone levels are a significant health concern, as are potential health impacts from chronic exposure to primary emissions of non-methane hydrocarbons (NMHC for residents living near wells. From measurements of ambient atmospheric NMHC present in residential areas located in close proximity to wells in Erie, Colorado, we find that mean mole fractions of the C2–C5 alkanes are enhanced by a factor of 18–77 relative to the regional background, and present at higher levels than typically found in large urban centers. When combined with NMHC observations from downtown Denver and Platteville, it is apparent that these compounds are elevated across the NFR, with highest levels within the Greater Wattenberg Gas Field. This represents a large area source for ozone precursors in the NFR. The BTEX aromatic compounds in Erie were comparable to (e.g., benzene or lower than (e.g., toluene, ethylbenzene, xylene in large urban centers, however, benzene was significantly higher in Platteville, and within the range of chronic health-based exposure levels. An initial look at comparisons with data sets from previous years reveal that ambient levels for oil and gas-related NMHC in Erie, as well as further downwind in Boulder, have not decreased, but appear to have been increasing, despite tightening of emissions standards for the oil and gas industries in 2008.

  6. Removal of vapor-phase elemental mercury from stack emissions with sulfur-impregnated activated carbon.

    Science.gov (United States)

    Sowlat, Mohammad Hossein; Abdollahi, Mohammad; Gharibi, Hamed; Yunesian, Masud; Rastkari, Noushin

    2014-01-01

    This systematic review of high-quality, relevant original research articles existing in the literature was conducted to comprehensively explore the efficiency of Hg11 capture from stack emissions by sulfur-impregnated vs. virgin ACs. Our systematic overview suggested that significantly higher amounts of Hg0 are absorbed by sulfurimpregnated ACs than by virgin ones ( 1.5-32 times higher, based on the applied operational conditions). The main reason for this is because Hg11 capture by virgin ACs follows a physisorption mechanism, whereas that by sulfur-impregnated ACs occurs from a combination of physisorption of Hg11 on carbon texture and chemical reaction between Hg0 and impregnated sulfur, with subsequent formation of HgS. Temperature increased the Hg0 adsorption capacity of virgin ACs, especially when temperatures exceeded 100 oc. For sulfur-impregnated ACs, increasing the temperature up to I 00 oc increased the Hg0 adsorption capacity by enhancing the chemisorption of Hg0 capture. A further increase in temperature enhanced the efficiency of ACs that were impregnated with Sat higher temperatures (600 °C, for instance). This mainly resulted from production of stronger bonding of sulfur to carbon at higher impregnation temperatures and also from a more even distribution of sulfur in the carbon matrix. The authors of different papers reported different results with respect to whether there is an effect of initial Hg11 concentration on AC adsorption capacity. The authors of two studies could find no such etl'ect. The predominant evidence, however, favors the view that increased Hg0 adsorption capacities exist at higher inlet Hg0 concentrations. Such behavior is attributed to faster kinetics of Hg0 capture and an enhanced higher driving force at higher initial Hg0 inlet concentrations. Results from reviewed studies also indicated that the optimum SIC ratio and sulfur content are 2/1 and I 0-20%, respectively. Surface area has a less significant impact on Hg11

  7. Study of NOx Emissions of S.I. Engine Fueled with Different Kinds of Hydrocarbon Fuels and Hydrogen

    Directory of Open Access Journals (Sweden)

    Qahtan A. Abass

    2010-01-01

    Full Text Available Liquefied petroleum gas (LPG, Natural gas (NG and hydrogen were used to operate spark ignition internal combustion engine Ricardo E6, to compare NOx emissions emitted from the engine, with that emitted from engine fueled with gasoline as a fuel.The study was done when engine operated at HUCR for gasoline, compared with its operation at HUCR for each fuel. Compression ratio, equivalence ratio and spark timing were studied at constant speed 25rps.The results appeared that NOx concentrations will be at maximum value in the lean side near the stoichiometric ratio, and reduced with moving away from this ratio for mixture at both sides, these concentrations were at its highest value when hydrogen used at CR=8:1, and got near to each other for the three hydrocarbon fuels used in the study, when the engine operated at HUCR for each fuel, but still hydrogen had maximum value, the main variable affect these concentrations was spark timing

  8. A New Star-Formation Rate Calibration from Polycyclic Aromatic Hydrocarbon Emission Features and Application to High Redshift Galaxies

    CERN Document Server

    Shipley, Heath V; Rieke, George H; Brown, Michael J I; Moustakas, John

    2016-01-01

    We calibrate the integrated luminosity from the polycyclic aromatic hydrocarbon (PAH) features at 6.2\\micron, 7.7\\micron\\ and 11.3\\micron\\ in galaxies as a measure of the star-formation rate (SFR). These features are strong (containing as much as 5-10\\% of the total infrared luminosity) and suffer minimal extinction. Our calibration uses \\spitzer\\ Infrared Spectrograph (IRS) measurements of 105 galaxies at $0 < z < 0.4$, infrared (IR) luminosities of $10^9 - 10^{12} \\lsol$, combined with other well-calibrated SFR indicators. The PAH luminosity correlates linearly with the SFR as measured by the extinction-corrected \\ha\\ luminosity over the range of luminosities in our calibration sample. The scatter is 0.14 dex comparable to that between SFRs derived from the \\paa\\ and extinction-corrected \\ha\\ emission lines, implying the PAH features may be as accurate a SFR indicator as hydrogen recombination lines. The PAH SFR relation depends on gas-phase metallicity, for which we supply an empirical correction for...

  9. Emission, distribution and toxicity of polycyclic aromatic hydrocarbons (PAHs) during municipal solid waste (MSW) and coal co-combustion.

    Science.gov (United States)

    Peng, Nana; Li, Yi; Liu, Zhengang; Liu, Tingting; Gai, Chao

    2016-09-15

    Emission and distribution characteristics of polycyclic aromatic hydrocarbons (PAHs) were investigated during municipal solid waste (MSW) and coal combustion alone and MSW/coal blend (MSW weight fraction of 25%) co-combustion within a temperature range of 500°C-900°C. The results showed that for all combustion experiments, flue gas occupied the highest proportion of total PAHs and fly ash contained more high-ring PAHs. Moreover, the 3- and 4-ring PAHs accounted for the majority of total PAHs and Ant or Phe had the highest concentrations. Compared to coal, MSW combustion generated high levels of total PAHs with the range of 111.28μg/g-10,047.22μg/g and had high toxicity equivalent value (TEQ). MSW/coal co-combustion generated the smallest amounts of total PAHs and had the lowest TEQ than MSW and coal combustion alone. Significant synergistic interactions occurred between MSW and coal during co-combustion and the interactions suppressed the formation of PAHs, especially hazardous high-ring PAHs and decreased the TEQ. The present study indicated that the reduction of the yield and toxicity of PAHs can be achieved by co-combustion of MSW and coal.

  10. Gas- and particle-phase distribution of polycyclic aromatic hydrocarbons in two-stroke, 50-cm 3 moped emissions

    Science.gov (United States)

    Spezzano, Pasquale; Picini, Paolo; Cataldi, Dario

    Gas- and particle-phase polycyclic aromatic hydrocarbons (PAHs) concentrations evaluated in the exhaust of 10 two-stroke, 50-cm 3 mopeds belonging to three different levels of emission legislation (EURO-0, EURO-1 and EURO-2) were used to assess the prevalent mechanism driving the gas/particle partitioning of PAHs in moped exhaust. Sampling was performed on a dynamometer bench both during the "cold-start" and the "hot" phases of the ECE-47 driving cycle. Gas and particulate phase PAHs were collected on polyurethane foam (PUF) plugs and 47-mm Pallflex T60A20 filters, respectively, under isokinetic conditions by using sampling probes inserted into the dilution tunnel of a Constant Volume Sampling - Critical Flow Venturi (CVS-CFV) system. The results show that semi-volatile PAHs were predominantly partitioned to the particle phase. The soluble organic fraction (SOF) of the collected particulates ranged between 72 and 98%. Measured total suspended particulate matter normalized partition coefficients ( Kp) were predicted within a factor of 3-5 by assuming absorption into the organic fraction according to a model developed by Harner and Bidleman [Harner, T., Bidleman, T.F., 1998. Octanol-air partition coefficient for describing particle/gas partitioning of aromatic compounds in urban air. Environmental Science & Technology 32, 1494-1502.]. This suggests that the gas/particle partitioning in moped exhaust is mainly driven by the high fraction of organic matter of the emitted particles and that absorption could be the main partitioning mechanism of PAHs.

  11. Pilot-Scale Demonstration of an Innovative Treatment for Vapor Emissions.

    Science.gov (United States)

    Watt, Andrew S; Magrini, Kimberly A; Carlson, Lynnae E; Wolfrum, Edward J; Larson, Sheldon A; Roth, Christine; Glatzmaier, Greg C

    1999-11-01

    Researchers from the National Renewable Energy Laboratory recently conducted a pilot-scale study at McClellan Air Force Base (AFB) in Sacramento, CA. The objective of the test was to determine the effectiveness of an ambient-temperature, solar-powered photocatalytic oxidation treatment unit for destroying emissions of chlorinated organic compounds from an air stripper. This paper reports test results and discusses applications and limitations of the technology. A 10-standard-cubic-foot-per-minute (SCFM) (28.3 L/min) slip stream of air from an air stripper at Operative Unit 29-31 at McClellan AFB was passed through a reactor that contained a lightweight, perforated, inert support coated with photoactive titanium dioxide. The reactor faced south and was tilted at a 45° angle from vertical so that the light-activated catalyst received most of the available sunlight. An online portable gas chro-matograph with two identical columns simultaneously analyzed the volatile organic compounds contained in the reactor inlet and outlet air streams. Summa canister grab samples of the inlet and outlet were also collected and sent to a certified laboratory for U.S. Environmental Protection Agency Method TO-14 analysis and verification of our field analyses. Three weeks of testing demonstrated that the treatment system's destruction and removal efficiencies (DREs) are greater than 95% at 10 SCFM with UV intensities at or greater than 1.5 milliwatts/square centimeter (mW/cm(2)). DREs greater than 95% at 20 SCFM were obtained under conditions where UV irradiation measured at or greater than 2 mW/cm(2). In Sacramento, this provided 6 hours of operation per clear or nearly clear day in April. A solar tracking system could extend operating time. The air stream also contained trace amounts of benzene. We observed no loss of system performance during testing.

  12. Hydrocarbon emissions from lean-burn natural gas engines. Kinetic modelling and visualization

    Energy Technology Data Exchange (ETDEWEB)

    Broe Bendtsen, A.

    1999-07-01

    Motivated by emissions of unburned fuel from natural gas engines, a detailed chemical kinetic model describing NO{sub x} sensitized oxidation of methane was developed. New methods for visualization of such complex models have been developed, based on chemometrics and explorative data analysis. They may find application in combustion chemistry and in atmospheric chemistry, where detailed kinetic models are widely used. The motivation of the project was the discovery of significant emissions of unburned fuel from natural gas engines. The thesis contains a brief summary of emission levels and the sources of these emissions. Results from experiments by the Danish Gas Technology Centre on a pilot scale engine showed that oxidation of methane may occur in an extended exhaust manifold. Based on these results experiments were initiated to obtain detailed knowledge of the governing oxidation chemistry in the exhaust manifold. A series of laboratory experiments showed that at a residence time of 200 ms the threshold temperature for oxidation of methane was lowered by 200 {kappa} from 1100 {kappa} to 900 {kappa} in the presence of NO or NO{sub 2}. Experiments with a residence time of 140 ms showed that the sensitizing effect of NO was related to a longer lag time, compared to effect of NO{sub 2}. The major product of oxidation from 900 {kappa} to 1100 {kappa} was CO. Published detailed chemical kinetic models were not able to describe these phenomena. It was attempted to modify existing kinetic models to describe this sensitization by estimation of reaction rates. A literature survey of various method for estimation of reaction rates is given, and one methods for estimation of reaction rates using Partial Least Squares regression is demonstrated, but only with moderate success. To obtain a better kinetic model, a conventional approach to the refinement of the kinetic model was assisted by visualization methods and explorative data analysis. Through this approach an existing

  13. Indirect global warming effects of ozone and stratospheric water vapor induced by surface methane emission

    Energy Technology Data Exchange (ETDEWEB)

    Wuebbles, D.J.; Grossman, A.S.; Tamaresis, J.S.; Patten, K.O. Jr.; Jain, A.; Grant, K.A.

    1994-07-01

    Methane has indirect effects on climate due to chemical interactions as well as direct radiative forcing effects as a greenhouse gas. We have calculated the indirect, time-varying tropospheric radiative forcing and GWP of O{sub 3} and stratospheric H{sub 2}O due to an impulse of CH{sub 4}. This impulse, applied to the lowest layer of the atmosphere, is the increase of the atmospheric mass of CH{sub 4} resulting from a 25 percent steady state increase in the current emissions as a function of latitude. The direct CH{sub 4} radiative forcing and GWP are also calculated. The LLNL 2-D radiative-chemistry-transport model is used to evaluate the resulting changes in the O{sub 3}, H{sub 2}O and CH{sub 4} atmospheric profiles as a function of time. A correlated k-distribution radiative transfer model is used to calculate the radiative forcing at the tropopause of the globally-averaged atmosphere profiles. The O{sub 3} indirect GWPs vary from {approximately}27 after a 20 yr integration to {approximately}4 after 500 years, agreeing with the previous estimates to within about 10 percent. The H{sub 2}O indirect GWPs vary from {approximately}2 after a 20 yr integration to {approximately}0.3 after 500 years, and are in close agreement with other estimates. The CH{sub 4} GWPs vary from {approximately}53 at 20 yrs to {approximately}7 at 500 yrs. The 20 year CH{sub 4} GWP is {approximately}20% larger than previous estimates of the direct CH{sub 4} GWP due to a CH{sub 4} response time ({approximately}17 yrs) that is much longer than the overall lifetime (10 yrs). The increased CH{sub 4} response time results from changes in the OH abundances caused by the CH{sub 4} impulse. The CH{sub 4} radiative forcing results are consistent with IPCC values. Estimates are made of latitude effects in the radiative forcing calculations, and UV effects on the O{sub 3} radiative forcing calculations (10%).

  14. Emissions of polycyclic aromatic hydrocarbons (PAHs) from the pyrolysis of scrap tires

    Science.gov (United States)

    Chen, Shui-Jen; Su, Hung-Bin; Chang, Juu-En; Lee, Wen-Jhy; Huang, Kuo-Lin; Hsieh, Lien-Te; Huang, Yi-Chu; Lin, Wen-Yinn; Lin, Chih-Chung

    This work investigated the PAHs generated in a waste-tire pyrolysis process and the PAHs removal by a wet scrubber (WSB) and a flare. IND, DBA, and BaP were found to dominate in the powders of scrap tires before the pyrolysis. The PAHs in the carbon blacks formed in the pyrolysis were mainly 2-, 3-, 6-, and 7-ring PAHs. Nap was the most predominant water-phase PAH in the WSB effluent. About 40% of the water-phase total-PAHs in the WSB effluent were contributed by nine carcinogenic PAHs. NaP, IND, and COR displayed higher mean gas- and particulate-phase concentrations than the other PAHs in the flare exhaust. The mean removal efficiencies of individual PAHs, total-PAHs, and high carcinogenic BaP+IND+DBA were 39.1-90.4%, 76.2%, and 84.9%, respectively for the WSB. For the flare, the mean removal efficiencies of gaseous, particulate, and combined (gaseous+particulate) total-PAHs were 59.8%, 91.2%, and 66.8%, respectively, whereas the removal efficiencies were 91.0%, 80.1%, and 89.1%, respectively for the total-BaPeq. However, the gaseous BaA displayed a negative mean removal efficiency. The total PAH emission rate and factor estimated for the scrap tire pyrolysis plant were 42.3 g d -1 and 4.00 mg kg-tire -1, respectively.

  15. Emission of mercury monobromide exciplex in gas-discharge plasma based on mixture of mercury dibromide vapor with sulfur hexafluoride and helium

    Science.gov (United States)

    Malinina, A. A.; Shuaibov, A. K.

    2011-02-01

    We present the results of investigations of an emission of a mercury monobromide exciplex in gas-discharge plasma of an atmospheric pressure barrier discharge based on a mixture of mercury dibromide vapor, sulfur hexafluoride, and helium. We optimized the emission power of mercury monobromide exciplexes with respect to the partial pressures of the working mixture. An average emission power of 0.42 W (λmax = 502 nm) is achieved in a cylindrical emission source with a small working volume (0.8 cm3) at a pumping pulse repetition rate of 6 kHz. We determined electron energy distribution functions, transport characteristics, specific discharge power losses for electron processes, electron concentration and temperature, as well as rate constants of elastic and inelastic scattering of electrons by components of the working mixture in relation to the ratio of the field strength to the total concentration of components of the working mixture. We discuss processes that increase the population of the mercury monobromide exciplex. Gas-discharge plasma created in a mixture of mercury dibromide vapor with sulfur hexafluoride and helium can be used as a working medium of an emission source in the blue-green spectral range for the use in scientific research in biotechnology, photonics, and medicine, as well as for creating indicator gas-discharge panels.

  16. A comparison on the emission of polycyclic aromatic hydrocarbons and their corresponding carcinogenic potencies from a vehicle engine using leaded and lead-free gasoline.

    Science.gov (United States)

    Mi, H H; Lee, W J; Tsai, P J; Chen, C B

    2001-12-01

    Our objective in this study was to assess the effect of using two kinds of lead-free gasoline [including 92-lead-free gasoline (92-LFG) and 95-lead-free gasoline (95-LFG), rated according to their octane levels] to replace the use of premium leaded gasoline (PLG) on the emissions of polycyclic aromatic hydrocarbons (PAHs) and their corresponding benzo[a]pyrene equivalent (BaP(eq)) amounts from the gasoline-powered engine. The results show that the three gasoline fuels originally contained similar total PAHs and total BaP(eq) contents; however, we found significant differences in the engine exhausts in both contents. The above results suggest that PAHs originally contained in the gasoline fuel did not affect the PAH emissions in the engine exhausts. The emission factors of both total PAHs and total BaP(eq) obtained from the three gasoline fuels shared the same trend: 95-LFG > PLG > 92-LFG. The above result suggests that when PLG was replaced by 95-LFG, the emissions would increase in both total PAHs and total BaP(eq), but when replaced by 92-LFG would lead to the decreased emissions of both contents. By taking emission factors and their corresponding annual gasoline consumption rates into account, we found that both total PAH and total BaP(eq) emissions increased from 1994 to 1999. However, the annual increasing rates in total BaP(eq) emissions were slightly higher than the corresponding increasing rates in total PAHs.

  17. Investigation of the composition of emissions from the vent of a carbon disulfide column condenser-cooler

    Energy Technology Data Exchange (ETDEWEB)

    Lisina, L.A.; Yaroslavskaya, T.A.; Ivanova, V.V.

    1983-01-01

    The gas-vapor mixture entering the atmosphere from the condenser-cooler vent consists not only of hydrocarbon vapors, but also noncondensing gases. On an increase in the temperature of the gas-vapor mixture there is an increase in the quantity of emissions, as well as an increase in the volatility of the hydrocarbons, with a decrease in the solubility of the gases. The noncondensing gases present in the crude benzol are apparently absorbed by the wash oil from the coke oven gas.

  18. Plant hydrocarbon recovery process

    Energy Technology Data Exchange (ETDEWEB)

    Dzadzic, P.M.; Price, M.C.; Shih, C.J.; Weil, T.A.

    1982-01-26

    A process for production and recovery of hydrocarbons from hydrocarbon-containing whole plants in a form suitable for use as chemical feedstocks or as hydrocarbon energy sources which process comprises: (A) pulverizing by grinding or chopping hydrocarbon-containing whole plants selected from the group consisting of euphorbiaceae, apocynaceae, asclepiadaceae, compositae, cactaceae and pinaceae families to a suitable particle size, (B) drying and preheating said particles in a reducing atmosphere under positive pressure (C) passing said particles through a thermal conversion zone containing a reducing atmosphere and with a residence time of 1 second to about 30 minutes at a temperature within the range of from about 200* C. To about 1000* C., (D) separately recovering the condensable vapors as liquids and the noncondensable gases in a condition suitable for use as chemical feedstocks or as hydrocarbon fuels.

  19. Slurry sampling fluorination assisted electrothermal vaporization-inductively coupled plasma-atomic emission spectrometry for the direct determination of metal impurities in aluminium oxide ceramic powders.

    Science.gov (United States)

    Peng, T; Chang, G; Wang, L; Jiang, Z; Hu, B

    2001-03-01

    A new analytical procedure for the direct determination of metal impurities (Cr, Cu, Fe and V) in aluminium oxide ceramic powders by slurry sampling fluorination assisted electrothermal vaporization-inductively coupled plasma-atomic emission spectrometry (ETV-ICP-AES) is reported. A polytetrafluoroethylene (PTFE) emulsion was used as a fluorinating reagent to promote the vaporization of impurity elements in aluminium oxide ceramic powders from the graphite tube. A vaporization stage with a long ramp time and a short hold time provided the possibility of temporal analyte-matrix separation. The experimental results indicated that a 10 microL 1% m/v slurry of aluminium oxide could be destroyed and vaporized completely with 600 micrograms PTFE under the selected conditions. Two aluminium oxide ceramic powder samples were used without any additional pretreatment. Analytical results obtained by using standard addition method with aqueous standard solution were checked by comparison of the results with pneumatic nebulization (PN)-ICP-AES based on the wet-chemical decomposition and analyte-matrix separation. The limits of detection (LODs) between 0.30 microgram g-1 (Fe) and 0.08 microgram g-1 (Cu) were achieved, and, the repeatability of measurements was mainly better than 10%.

  20. Polycyclic aromatic hydrocarbons and nitropolycyclic aromatic hydrocarbons in urban air particulates and their relationship to emission sources in the Pan-Japan Sea countries

    Energy Technology Data Exchange (ETDEWEB)

    Tang, N.; Hattori, T.; Taga, R.; Igarashi, K.; Yang, X.Y.; Tamura, K.; Kakimoto, H.; Mishukov, V.F.; Toriba, A.; Kizu, R.; Hayakawa, K. [Kanazawa University, Kanazawa (Japan)

    2005-10-01

    Airborne particulates were collected in seven cities in the Pan-Japan Sea countries, Shenyang (China), Vladivostok (Russia), Seoul (South Korea), Kitakyushu, Kanazawa, Tokyo and Sapporo (Japan), in winter and summer from 1997 to 2002. In addition, particulates from domestic coal-burning heaters and diesel engine automobiles were collected in Shenyang and Kanazawa, respectively. Nine polycyclic aromatic hydrocarbons (PAHs) and four nitropolycyclic aromatic hydrocarbons (NPAHs) in the extracts from the particulates were analysed by HPLC with fluorescence and chemiluminescence detections, respectively. Mean atmospheric concentrations of PAHs in Shenyang and Vladivostok were substantially higher than those in Seoul, Tokyo, Sapporo, Kitakyushu and Kanazawa. However, the mean atmospheric concentrations of NPAHs were at the same levels in all cities except Kitakyushu. The expected seasonal variations (greater PAH and NPAH concentrations in winter than in summer) were observed in all cities. In order to study the major contributors of atmospheric PAHs and NPAHs, both cluster analysis and factor analysis were used and three large clusters were identified. The 1-nitropyrene/pyrene concentration ratio seemed to be a suitable indicator of the contribution made by diesel-engine vehicles and coal combustion to urban air particulates.

  1. Hydrocarbon pneumonia

    Science.gov (United States)

    Pneumonia - hydrocarbon ... Coughing Fever Shortness of breath Smell of a hydrocarbon product on the breath Stupor (decreased level of ... Most children who drink or inhale hydrocarbon products and develop ... hydrocarbons may lead to rapid respiratory failure and death.

  2. A comparative study of nitrogen plasma effect on field emission characteristics of single wall carbon nanotubes synthesized by plasma enhanced chemical vapor deposition

    Science.gov (United States)

    Kumar, Avshish; Parveen, Shama; Husain, Samina; Ali, Javid; Zulfequar, Mohammad; Harsh; Husain, Mushahid

    2014-12-01

    Vertically aligned single wall carbon nanotubes (SWCNTs) with large scale control of diameter, length and alignment have successfully been grown by plasma enhanced chemical vapor deposition (PECVD) system. The nickel (Ni) as catalyst deposited on silicon (Si) substrate was used to grow the SWCNTs. Field emission (FE) characteristics of the as grown SWCNTs were measured using indigenously designed setup in which a diode is configured in such a way that by applying negative voltage on the copper plate (cathode) with respect to stainless steel anode plate, current density can be recorded. To measure the FE characteristics, SWCNTs film pasted on the copper plate with silver epoxy was used as electron emitter source. The effective area of anode was ∼78.5 mm2 for field emission measurements. The emission measurements were carried out under high vacuum pressure of the order of 10-6 Torr to minimize the electron scattering and degradation of the emitters. The distance between anode and cathode was kept 500 μm (constant) during entire field emission studies. The grown SWCNTs are excellent field emitters, having emission current density higher than 25 mA/cm2 at turn-on field 1.3 V/μm. In order to enhance the field emission characteristics, the as grown SWCNTs have been treated under nitrogen (N2) plasma for 5 min and again field emission characteristics have been measured. The N2 plasma treated SWCNTs show a good enhancement in the field emission properties with emission current density 81.5 mA/cm2 at turn on field 1.2 V/μm. The as-grown and N2 plasma treated SWCNTs were also characterized by field emission scanning electron microscope (FESEM), high resolution transmission electron microscope (HRTEM), Raman spectrometer, Fourier transform infrared spectrometer (FTIR) and X-ray photoelectron spectroscopy (XPS).

  3. Vapor pressure studies of the solubilization of hydrocarbons by surfactant micelles. Final report, April 1, 1984-December 31, 1984. [Solubilization data for system benzene/sodium octylsulfate/sodium chloride/water at 15/sup 0/, 25/sup 0/, 35/sup 0/ and 45/sup 0/C

    Energy Technology Data Exchange (ETDEWEB)

    Christian, S.D.; Tucker, E.E.

    1985-04-01

    This final report describes vapor pressure studies of the solubilization of hydrocarbons and hydrocarbon derivatives by aqueous micellar solutions. An automated vapor pressure apparatus and a manual apparatus incorporating a mercury-covered sintered-glass disk inlet valve were used to obtain highly precise data for the solubilization of hydrocarbons and aliphatic alcohols into aqueous solutions of the ionic surfactants sodium octylsulfate and n-hexadecylpyridinium chloride (cetylpyridinium chloride). A mass-action model based on a modification of the Poisson distribution equations has been developed and applied to data for the system benzene/sodium octylsulfate/sodium chloride/water at 15/sup 0/, 25/sup 0/, 35/sup 0/, and 45/sup 0/C. An excellent goodness of fit is achieved with the model. Tabulated experimental results (485 sets of activity and concentration data) are included in this report. 12 references, 2 figures.

  4. Gasoline Reid Vapor Pressure

    Science.gov (United States)

    EPA regulates the vapor pressure of gasoline sold at retail stations during the summer ozone season to reduce evaporative emissions from gasoline that contribute to ground-level ozone and diminish the effects of ozone-related health problems.

  5. The application of forest classification from Landsat data as a basis for natural hydrocarbon emission estimation and photochemical oxidant model simulations in southeastern Virginia

    Science.gov (United States)

    Salop, J.; Wakelyn, N. T.; Levy, G. F.; Middleton, W. M.; Gervin, J. C.

    1983-01-01

    The possible contribution by natural hydrocarbon emissions to the total ozone budget recorded in the Tidewater region of southeastern Virginia during the height of the summer period was examined. Natural sources investigated were limited to the primary HC emitters and most prevalent natural vegetation, the forests. Three types and their areal coverage were determined for Region VI of the Virginia State Air Pollution Control Board using remotely sensed data from Landsat, a NASA experimental earth resources satellite. Emission factors appropriate to the specific types (coniferous 0.24 x 10 to the 13th, mixed 0.63 x 10 to the 13th, deciduous 1.92 x 10 to the 13th, microgram/h), derived from contemporary procedures, were applied to produce an overall regional emission rate of 2.79 x 10 to the 13th microgram/h for natural non-methane hydrocarbons (NMHC). This rate was used with estimates of the anthropogenic NO(x) and NMHC loading, as input into a photochemical box model. Additional HC loading on the order of that estimated to be produced by the natural forest communities was required in order to reach certain measured summer peak ozone levels as the computer simulation was unable to account for the measured episodic levels on the basis of the anthropogenic inventory alone.

  6. Enrichment of light hydrocarbon mixture

    Science.gov (United States)

    Yang; Dali; Devlin, David; Barbero, Robert S.; Carrera, Martin E.; Colling, Craig W.

    2010-08-10

    Light hydrocarbon enrichment is accomplished using a vertically oriented distillation column having a plurality of vertically oriented, nonselective micro/mesoporous hollow fibers. Vapor having, for example, both propylene and propane is sent upward through the distillation column in between the hollow fibers. Vapor exits neat the top of the column and is condensed to form a liquid phase that is directed back downward through the lumen of the hollow fibers. As vapor continues to ascend and liquid continues to countercurrently descend, the liquid at the bottom of the column becomes enriched in a higher boiling point, light hydrocarbon (propane, for example) and the vapor at the top becomes enriched in a lower boiling point light hydrocarbon (propylene, for example). The hollow fiber becomes wetted with liquid during the process.

  7. A comparison on the emission of polycyclic aromatic hydrocarbons and their corresponding carcinogenic potencies from a vehicle engine using leaded and lead-free gasoline.

    OpenAIRE

    Mi, H H; Lee, W J; Tsai, P.J.; Chen, C B

    2001-01-01

    Our objective in this study was to assess the effect of using two kinds of lead-free gasoline [including 92-lead-free gasoline (92-LFG) and 95-lead-free gasoline (95-LFG), rated according to their octane levels] to replace the use of premium leaded gasoline (PLG) on the emissions of polycyclic aromatic hydrocarbons (PAHs) and their corresponding benzo[a]pyrene equivalent (BaP(eq)) amounts from the gasoline-powered engine. The results show that the three gasoline fuels originally contained sim...

  8. Emission characteristics of a barrier discharge in an argon-freon-water vapor mixture in the UV-VUV spectral range

    Science.gov (United States)

    Shuaibov, A. K.; Minya, A. I.; Gomoki, Z. T.; Gritsak, R. V.

    2013-05-01

    Optical characteristics of an ArCl*-OH* lamp excited by a nanosecond barrier discharge are studied. This discharge is a source of the ArCl ( B → X), ( D' → A'), and OH( A → X) molecular band emission with peaks at 175, 258, and 309 nm, respectively. The intensity of the barrier discharge plasma radiation is optimized as a function of the CCl4 vapor partial pressure at p(Ar) = 24 kPa and p(H2O) = 10-20 Pa.

  9. Atmospheric emissions from the Deepwater Horizon spill constrain air-water partitioning, hydrocarbon fate, and leak rate

    Science.gov (United States)

    Ryerson, T. B.; Aikin, K. C.; Angevine, W. M.; Atlas, E. L.; Blake, D. R.; Brock, C. A.; Fehsenfeld, F. C.; Gao, R.-S.; de Gouw, J. A.; Fahey, D. W.; Holloway, J. S.; Lack, D. A.; Lueb, R. A.; Meinardi, S.; Middlebrook, A. M.; Murphy, D. M.; Neuman, J. A.; Nowak, J. B.; Parrish, D. D.; Peischl, J.; Perring, A. E.; Pollack, I. B.; Ravishankara, A. R.; Roberts, J. M.; Schwarz, J. P.; Spackman, J. R.; Stark, H.; Warneke, C.; Watts, L. A.

    2011-04-01

    The fate of deepwater releases of gas and oil mixtures is initially determined by solubility and volatility of individual hydrocarbon species; these attributes determine partitioning between air and water. Quantifying this partitioning is necessary to constrain simulations of gas and oil transport, to predict marine bioavailability of different fractions of the gas-oil mixture, and to develop a comprehensive picture of the fate of leaked hydrocarbons in the marine environment. Analysis of airborne atmospheric data shows massive amounts (˜258,000 kg/day) of hydrocarbons evaporating promptly from the Deepwater Horizon spill; these data collected during two research flights constrain air-water partitioning, thus bioavailability and fate, of the leaked fluid. This analysis quantifies the fraction of surfacing hydrocarbons that dissolves in the water column (˜33% by mass), the fraction that does not dissolve, and the fraction that evaporates promptly after surfacing (˜14% by mass). We do not quantify the leaked fraction lacking a surface expression; therefore, calculation of atmospheric mass fluxes provides a lower limit to the total hydrocarbon leak rate of 32,600 to 47,700 barrels of fluid per day, depending on reservoir fluid composition information. This study demonstrates a new approach for rapid-response airborne assessment of future oil spills.

  10. Direct determination of sulfur species in coals from the Argonne premium sample program by solid sampling electrothermal vaporization inductively coupled plasma optical emission spectrometry.

    Science.gov (United States)

    Bauer, Daniela; Vogt, Thomas; Klinger, Mathias; Masset, Patrick Joseph; Otto, Matthias

    2014-10-21

    A new direct solid sampling method for speciation of sulfur in coals by electrothermal vaporization inductively coupled plasma optical emission spectrometry (ETV-ICP OES) is presented. On the basis of the controlled thermal decomposition of coal in an argon atmosphere, it is possible to determine the different sulfur species in addition to elemental sulfur in coals. For the assignment of the obtained peaks from the sulfur transient emission signal, several analytical techniques (reflected light microscopy, scanning electron microscopy with energy dispersive X-ray spectroscopy and X-ray diffraction) were used. The developed direct solid sampling method enables a good accuracy (relative standard deviation ≤ 6%), precision and was applied to determine the sulfur forms in the Argonne premium coals, varying in rank. The generated method is time- and cost-effective and well suited for the fast characterization of sulfur species in coal. It can be automated to a large extent and is applicable for process-accompanying analyses.

  11. Nonradioactive Environmental Emissions Chemical Source Term for the Double Shell Tank (DST) Vapor Space During Waste Retrieval Operations

    Energy Technology Data Exchange (ETDEWEB)

    MAY, T.H.

    2000-04-21

    A nonradioactive chemical vapor space source term for tanks on the Phase 1 and the extended Phase 1 delivery, storage, and disposal mission was determined. Operations modeled included mixer pump operation and DST waste transfers. Concentrations of ammonia, specific volatile organic compounds, and quantitative volumes of aerosols were estimated.

  12. Role of the concentration and nature of grafted groups in the adsorption of hydrocarbon vapors on silica modified by monofunctional polyfluoroalkylsilanes

    Science.gov (United States)

    Roshchina, T. M.; Shoniya, N. K.; Tayakina, O. Ya.; Tkachenko, O. P.; Kustov, L. M.; Bernardoni, F.; Fadeev, A. Y.

    2012-03-01

    The role of the grafting density of monofunctional polyfluoroalkylsilanes of the C n F2 n - 1(CH2) m Si(CH3)2Cl general formula (where n = 3, 4, and 6; and m = 2 and 3) and their composition in intermolecular interactions of the molecules of saturated and aromatic hydrocarbons with a surface of chemically modified silica is studied by means of IR spectroscopy and adsorption-static and gas chromatography. It is shown that the higher the concentration and the shorter the length of the grafted chain, the greater (by a factor of 2 to 25) the drop in the adsorption values of hydrocarbons as a result of modifications, due to an increase in the degree of oleophobization of surface upon the formation of polyorganofluorine coatings. The high specificity of the surface with respect to benzene, which is due to the active participation of the polar fragment of a grafted chain in adsorption process, is related to the features of a relatively low-density sample with a concentration of grafted perfluorobutyl groups of 1.7 nm-2. It is shown that the thermodestruction of polyfluoroalkyl silica remains virtually unobserved upon heating to 523 K in an argon flow.

  13. Modeling and Multi-Objective Optimization of Engine Performance and Hydrocarbon Emissions via the Use of a Computer Aided Engineering Code and the NSGA-II Genetic Algorithm

    Directory of Open Access Journals (Sweden)

    Richard Fiifi Turkson

    2016-01-01

    Full Text Available It is feared that the increasing population of vehicles in the world and the depletion of fossil-based fuel reserves could render transportation and other activities that rely on fossil fuels unsustainable in the long term. Concerns over environmental pollution issues, the high cost of fossil-based fuels and the increasing demand for fossil fuels has led to the search for environmentally friendly, cheaper and efficient fuels. In the search for these alternatives, liquefied petroleum gas (LPG has been identified as one of the viable alternatives that could be used in place of gasoline in spark-ignition engines. The objective of the study was to present the modeling and multi-objective optimization of brake mean effective pressure and hydrocarbon emissions for a spark-ignition engine retrofitted to run on LPG. The use of a one-dimensional (1D GT-Power™ model, together with Group Method of Data Handling (GMDH neural networks, has been presented. The multi-objective optimization was implemented in MATLAB® using the non-dominated sorting genetic algorithm (NSGA-II. The modeling process generally achieved low mean squared errors (0.0000032 in the case of the hydrocarbon emissions model for the models developed and was attributed to the collection of a larger training sample data using the 1D engine model. The multi-objective optimization and subsequent decisions for optimal performance have also been presented.

  14. Optimization of the operating conditions of solid sampling electrothermal vaporization coupled to inductively coupled plasma optical emission spectrometry for the sensitive direct analysis of powdered rice.

    Science.gov (United States)

    Sadiq, Nausheen; Beauchemin, Diane

    2014-12-03

    Two different approaches were used to improve the capabilities of solid sampling (SS) electrothermal vaporization (ETV) coupled to inductively coupled plasma optical emission spectrometry (ICP-OES) for the direct analysis of powdered rice. Firstly, a cooling step immediately before and after the vaporization step in the ETV temperature program resulted in a much sharper analyte signal peak. Secondly, point-by-point internal standardization with an Ar emission line significantly improved the linearity of calibration curves obtained with an increasing amount of rice flour certified reference material (CRM). Under the optimized conditions, detection limits ranged from 0.01 to 6ngg(-1) in the solid, depending on the element and wavelength selected. The method was validated through the quantitative analysis of corn bran and wheat flour CRMs. Application of the method to the multi-elemental analysis of 4-mg aliquots of real organic long grain rice (white and brown) also gave results for Al, As, Co, Cu, Fe, Mg, Se, Pb and Zn in agreement with those obtained by inductively coupled plasma mass spectrometry following acid digestion of 0.2-g aliquots. As the analysis takes roughly 5min per sample (2.5min for grinding, 0.5-1min for weighing a 4-mg aliquot and 87s for the ETV program), this approach shows great promise for fast screening of food samples.

  15. Performance Evaluations and Quality Validation System for Optical Gas Imaging Cameras That Visualize Fugitive Hydrocarbon Gas Emissions

    Science.gov (United States)

    Optical gas imaging (OGI) cameras have the unique ability to exploit the electromagnetic properties of fugitive chemical vapors to make invisible gases visible. This ability is extremely useful for industrial facilities trying to mitigate product losses from escaping gas and fac...

  16. Estimation of the efficiency of hydrocarbon mineralization in soil by measuring CO2-emission and variations in the isotope composition of carbon dioxide

    Science.gov (United States)

    Dubrovskaya, Ekaterina; Turkovskaya, Olga

    2010-05-01

    Estimation of the efficiency of hydrocarbon mineralization in soil by measuring CO2-emission and variations in the isotope composition of carbon dioxide E. Dubrovskaya1, O. Turkovskaya1, A. Tiunov2, N. Pozdnyakova1, A. Muratova1 1 - Institute of Biochemistry and Physiology of Plants and Microorganisms, RAS, Saratov, 2 - A.N. Severtsov Institute of Ecology and Evolution, RAS, Moscow, Russian Federation Hydrocarbon mineralization in soil undergoing phytoremediation was investigated in a laboratory experiment by estimating the variation in the 13С/12С ratio in the respired СО2. Hexadecane (HD) was used as a model hydrocarbon pollutant. The polluted soil was planted with winter rye (Secale cereale) inoculated with Azospirillum brasilense strain SR80, which combines the abilities to promote plant growth and to degrade oil hydrocarbon. Each vegetated treatment was accompanied with a corresponding nonvegetated one, and uncontaminated treatments were used as controls. Emission of carbon dioxide, its isotopic composition, and the residual concentration of HD in the soil were examined after two and four weeks. At the beginning of the experiment, the CO2-emission level was higher in the uncontaminated than in the contaminated soil. After two weeks, the quantity of emitted carbon dioxide decreased by about three times and did not change significantly in all uncontaminated treatments. The presence of HD in the soil initially increased CO2 emission, but later the respiration was reduced. During the first two weeks, nonvegetated soil had the highest CO2-emission level. Subsequently, the maximum increase in respiration was recorded in the vegetated contaminated treatments. The isotope composition of plant material determines the isotope composition of soil. The soil used in our experiment had an isotopic signature typical of soils formed by C3 plants (δ13C,-22.4‰). Generally, there was no significant fractionation of the carbon isotopes of the substrates metabolized by the

  17. Field evaluation of a new plastic film (vapor safe) to reduce fumigant emissions and improve distribution in soil.

    Science.gov (United States)

    Qin, Ruijun; Gao, Suduan; Ajwa, Husein; Sullivan, David; Wang, Dong; Hanson, Bradley D

    2011-01-01

    Preplant soil fumigation is an important pest management practice in coastal California strawberry production regions. Potential atmospheric emissions of fumigants from field treatment, however, have drawn intensive environmental and human health concerns; increasingly stringent regulations on fumigant use have spurred research on low-emission application techniques. The objectives of this research were to determine the effects of a new low-permeability film, commonly known as totally impermeable film (TIF), on fumigant emissions and on fumigant distribution in soil. A 50/50 mixture of 1,3-dichloropropene (1,3-D) and chloropicrin (CP) was shank-applied at 314 kg ha in two location-separate field plots (0.4 ha each) in Ventura County, California, in fall 2009. One plot was surface-covered with standard polyethylene (PE) film, and the other was covered with TIF immediately after fumigant application. Data collection included emissions, soil-gas phase concentration profile, air concentration under the film, and soil residuals of the applied fumigants. Peak emission flux of 1,3-D and CP from the TIF field was substantially lower than from the PE field. Total through-film emission loss was 2% for 1,3-D and emission surge compared with the PE field, while CP emissions were fairly low in both fields. Higher concentrations and a more uniform distribution in the soil profile for 1,3-D and CP were observed under the TIF compared with the PE film, suggesting that the TIF may allow growers to achieve satisfactory pest control with lower fumigant rates. The surging 1,3-D emissions after film-cutting could result in high exposure risks to workers and bystanders and must be addressed with additional mitigation measures.

  18. Constraints on emissions of carbon monoxide, methane, and a suite of hydrocarbons in the Colorado Front Range using observations of 14CO2

    Directory of Open Access Journals (Sweden)

    P. P. Tans

    2013-01-01

    Full Text Available Atmospheric radiocarbon (14CO represents an important observational constraint on emissions of fossil-fuel derived carbon into the atmosphere due to the absence of 14CO in fossil fuel reservoirs. The high sensitivity and precision that accelerator mass spectrometry (AMS affords in atmospheric 14CO analysis has greatly increased the potential for using such measurements to evaluate bottom-up emissions inventories of fossil fuel CO2 (CO2ff, as well as those for other co-emitted species. Here we use observations of 14CO2 and a series of hydrocarbons and combustion tracers from discrete air samples collected between June 2009 and September 2010 at the National Oceanic and Atmospheric Administration Boulder Atmospheric Observatory (BAO; Lat: 40.050° N, Lon: 105.004° W to derive emission ratios of each species to CO2ff. From these emission ratios, we estimate emissions of these species by using the Vulcan CO2ff high resolution data product as a reference. The species considered in this analysis are carbon monoxide (CO, methane (CH4, acetylene (C2H2, benzene (C6H6, and C3–C5 alkanes. Comparisons of top-down emissions estimates are made to existing inventories of these species for Denver and adjacent counties, as well as to previous efforts to estimate emissions from atmospheric observations over the same area. We find that CO is overestimated in the 2008 National Emissions Inventory (NEI, 2008 by a factor of ~2. A close evaluation of the inventory suggests that the ratio of CO emitted per unit fuel burned from on-road gasoline vehicles is likely over-estimated by a factor of 2.5. The results also suggest that while the oil and gas sector is the largest contributor to the CH4 signal in air arriving from the north and east, it is very likely that other sources, including agricultural sources, contribute to this signal and must be accounted for when attributing these signals to oil and gas industry activity from a top-down perspective. Our results are

  19. Identification of emission sources of particle-bound polycyclic aromatic hydrocarbons in the vicinity of the industrial zone of the city of Novi Sad

    Directory of Open Access Journals (Sweden)

    Jovčić Nataša S.

    2013-01-01

    Full Text Available Data on polycyclic aromatic hydrocarbons (PAHs in ambient air accessed at selected locations in the vicinity of the industrial zone of the city of Novi Sad, Serbia, have been presented and analyzed in order to determine seasonal and spatial variations and to identify emission sources of particle-bound PAHs. Previous studies have demonstrated that the major contributors of PAHs in urban areas are the emissions from vehicle exhaust, and emissions releases from industrial processes like aluminium production, creosote and wood preservation, waste incineration, cement manufacture, petrochemical and related industries, commercial heat/power production etc. The sampling campaigns have been conducted at three sampling sites, during the two 14-day periods. The first site was situated near industrial area, with a refinery, power plant and heavy-traffic road in the vicinity. The second site was located nearby the heavy traffic area, especially busy during the rush hour. The third site was residential district. Summer sampling period lasted from June 26th to July 10th 2008, while sampling of ambient air during the winter was undertaken from January 22nd to February 5th 2009. Eighty-four (84 air samples were collected using a high volume air sampler TCR Tecora H0649010/ECHO. 16 US EPA polycyclic aromatic hydrocarbons were determined in all samples using a gas chromatographer with a mass spectrometer as a detector (Shimatzu MDGC/GCMS-2010. The total average concentrations of PAHs ranged from 1.21 to 1.77 ng/m3 during the summer period and from 6.31 to 7.25 ng/m3 in the winter. Various techniques, including diagnostic ratio (DR and principal component analysis (PCA, have been used to define and evaluate potential emission sources of PAHs. Diagnostic ratio analysis indicated that vehicles, diesel or/and gasoline, industrial and combustion emissions were sources of PAHs in the vicinity of the industrial zone. Additionally, principal component analysis was used

  20. Sensitive determination of mercury in tap water by cloud point extraction pre-concentration and flow injection-cold vapor-inductively coupled plasma optical emission spectrometry

    Science.gov (United States)

    de Wuilloud, Jorgelina C. A.; Wuilloud, Rodolfo G.; Silva, María. F.; Olsina, Roberto A.; Martinez, Luis D.

    2002-02-01

    A pre-concentration and determination methodology for mercury at trace levels in water samples was developed. Cloud point extraction was successfully employed for the pre-concentration of mercury prior to inductively coupled plasma optical emission spectrometry coupled to a flow injection with cold vapor generation system. The mercury was extracted as mercury-2-(5-bromo-2-pyridylazo)-5-diethylaminophenol [Hg(II)-(5-Br-PADAP)] complex, at pH 9.2 mediated by micelles of the non-ionic surfactant polyethyleneglycolmono- p-nonylphenylether (PONPE 5). Cold vapor generation was developed from 100 μl of the extracted surfactant-rich phase by means of a stannous chloride (SnCl 2) solution as reluctant. An exhaustive study of the variables affecting the cloud point extraction with PONPE 5 and cold vapor mercury generation from the surfactant phase was performed. The 50-ml sample solution pre-concentration allowed us to raise an enrichment factor of 200-fold. The lower limit of detection obtained under the optimal conditions was 4 ng l -1. The precision for 10 replicate determinations at the 0.5-μg l -1 Hg level was 3.4% relative standard deviation (R.S.D.), calculated with the peak heights. The calibration graph using the pre-concentration system for mercury was linear with a correlation coefficient of 0.9998 at levels near the detection limits up to at least 50 μg l -1. The method was successfully applied to the determination of mercury in tap water samples.

  1. Determination of Se in biological samples by axial view inductively coupled plasma optical emission spectrometry after digestion with aqua regia and on-line chemical vapor generation

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Eder Jose dos [Instituto de Tecnologia do Parana (TECPAR), 81350-010 Curitiba, PR (Brazil)], E-mail: eder@tecpar.br; Herrmann, Amanda Beatriz; Kulik de Caires, Suzete [Instituto de Tecnologia do Parana (TECPAR), 81350-010 Curitiba, PR (Brazil); Azzolin Frescura, Vera Lucia; Curtius, Adilson Jose [Departamento de Quimica, Universidade Federal de Santa Catarina (UFSC), 880400-900 Florianopolis, SC (Brazil)

    2009-06-15

    A simple and fast method for the determination of Se in biological samples, including food, by axial view inductively coupled plasma optical emission spectrometry using on-line chemical vapor generation (CVG-ICP OES) is proposed. The concentrations of HCl and NaBH{sub 4}, used in the chemical vapor generation were optimized by factorial analysis. Six certified materials (non-fat milk powder, lobster hepatopancreas, human hair, whole egg powder, oyster tissue, and lyophilised pig kidney) were treated with 10 mL of aqua regia in a microwave system under reflux for 15 min followed by additional 15 min in an ultrasonic bath. The solutions were transferred to a 100 mL volumetric flask and the final volume was made up with water. The Se was determined directly in these solutions by CVG-ICP OES, using the analytical line at 196.026 nm. Calibration against aqueous standards in 10% v/v aqua regia in the concentration range of 0.5-10.0 {mu}g L{sup -} {sup 1} Se(IV) was used for the analysis. The quantification limit, considering a 0.5 g sample weight in a final volume of 100 mL{sup -} {sup 1} was 0.10 {mu}g g{sup -} {sup 1}. The obtained concentration values were in agreement with the total certified concentrations, according to the t-test for a 95% confidence level.

  2. [An investigation of the formation of] polycyclic aromatic hydrocarbon (PAH) emissions when firing pulverized coal in a bench-scale drop tube reactor

    Energy Technology Data Exchange (ETDEWEB)

    Pisupati, S.V.; Wasco, R.S.; Scaroni, A.W. [Pennsylvania State Univ., University Park, PA (United States). Combustion Lab.

    1998-12-31

    The Clean Air Act Amendments (CAAA) of 1990 contain provisions which will set standards for the allowable emissions of 188 analytes designated as hazardous air pollutants (HAPs). This list of HAPs was used to establish an initial list of source categories for which EPA would be required to establish technology-based emission standards, which would result in regulated sources sharply reducing routine emissions of toxic air pollutants. Polycyclic organic matter (POM) has also been referred to as polynuclear or polycyclic aromatic compounds (PACs). Nine major categories of POM have been defined by EPA. The study of organic compounds from coal combustion is complex and the results obtained so far are inconclusive with respect to emission factors. The most common organic compounds in the flue gas of coal-fired power plants are polycyclic aromatic hydrocarbons (PAHs). Furthermore, EPA has specified 16 PAH compounds as priority pollutants. These are naphthalene, acenaphthylene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, chrysene, benz[a]anthracene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, indeno[1,2,3-cd]pyrene, benzo[ghi]perylene, and dibenz[ah]anthracene. Penn State`s Combustion Laboratory is equipped to collect and analyze the HAPs in the flue gas from fossil fuels combustion. The overall objective of this study was to examine the effect of unit temperature on PAH emissions. A Modified Method 5 sampling train was used to isokinetically collect samples at desired locations in flue gas streams. The collected sample can be separated into solid, condensed liquid and gaseous phases. The PAHs of interest are extracted from the collected sample, concentrated, then separated and quantified by gas chromatography/mass spectrometry (GC/MS). This study was conducted using a bench-scale drop-tube reactor (DTR). The fuel selected for this study was a Middle Kittanning seam coal pulverized to 80% passing US Standard 200 mesh (commonly

  3. Impact of using fishing boat fuel with high poly aromatic content on the emission of polycyclic aromatic hydrocarbons from the diesel engine

    Science.gov (United States)

    Lin, Yuan-Chung; Lee, Wen-Jhy; Li, Hsing-Wang; Chen, Chung-Ban; Fang, Guor-Cheng; Tsai, Perng-Jy

    Because of the fishery subsidy policy, the fishing boat fuel oil (FBFO) exemption from commodity taxes, business taxes and air pollution control fees, resulted in the price of FBFO was ˜50% lower than premium diesel fuel (PDF) in Taiwan. It is estimated that ˜650,000 kL FBFO was illegally used by traveling diesel-vehicles (TDVs) with a heavy-duty diesel engine (HDDE), which accounted for ˜16.3% of the total diesel fuel consumed by TDVs. In this study, sulfur, poly aromatic and total-aromatic contents in both FBFO and PDF were measured and compared. Exhaust emissions of polycyclic aromatic hydrocarbons (PAHs) and their carcinogenic potencies (BaP eq) from a HDDE under transient cycle testing for both FBFO and PDF were compared and discussed. Finally, the impact caused by the illegal use of FBFO on the air quality was examined. Results show that the mean sulfur-, poly aromatic and aromatic-contents in FBFO were 43.0, 3.89 and 1.04 times higher than that of PDF, respectively. Emission factors of total-PAHs and total-BaP eq obtained by utilizing FBFO were 51.5 and 0.235 mg L -1-Fuel, which were 3.41 and 5.82 times in magnitude higher than obtained by PDF, respectively. The estimated annual emissions of total-PAHs and total-BaP eq to the ambient environment due to the illegally used FBFO were 23.6 and 0.126 metric tons, respectively, which resulted in a 17.9% and a 25.0% increment of annual emissions from all mobile sources, respectively. These results indicated that the FBFO used illegally by TDVs had a significant impact on PAH emissions to the ambient environment.

  4. Mechanism of light emission and manufacturing process of vertical-type light-emitting diode grown by hydride vapor phase epitaxy

    Science.gov (United States)

    Lee, Gang Seok; Jeon, Hunsoo; Ahn, Hyung Soo; Yang, Min; Yi, Sam Nyung; Yu, Young Moon; Lee, Sang Chil; Honda, Yoshio; Sawaki, Nobuhiko; Kim, Suck-Whan

    2017-01-01

    We developed a vertical-type light-emitting diode (LED) in which the substrate is removed using a hydride vapor phase epitaxy (HVPE) apparatus consisting of a multi-graphite boat filled with a mixed source and a high-temperature (T ≈ 900 °C) RF heating coil outside the source zone. The new chip-growth process with a significant reduction in the number of production steps is completed in only four steps, namely, photolithography, epitaxial layer growth, sorting, and metallization. We analyze the emission mechanism of these lights from measurement results to validate the characteristics of the light emitted from these vertical-type blue LEDs and white LEDs (WLEDs) without substrates, and propose that this mixed-source HVPE method may be a promising production technique for LEDs.

  5. Trace determination of Hg together with As, Sb, Se by miniaturized optical emission spectrometry integrated with chemical vapor generation and capacitively coupled argon microwave miniplasma discharge

    Science.gov (United States)

    Matusiewicz, Henryk; Ślachciński, Mariusz

    2017-07-01

    A miniaturized optical emission spectrometer (OES) with capacitively coupled argon microwave microplasma (μCMP) as and excitation source and chemical vapor generation (CVG) for sample introduction was constructed for the determination of trace Hg, As, Sb and Se. The applied method enabled simultaneous determination of hydride-forming elements (As, Sb, Se) and volatile Hg. Mercury cold vapor and the hydride volatile species of As, Sb and Se were generated when standard or sample solutions were separated from the liquid phase for transport to the capacitively coupled microwave microplasma and detection of their atomic emission. A univariate approach and the simplex optimization procedure were used to achieve optimized conditions and derive analytical figures of merit. The experimental concentration detection limits (LODs) for simultaneous determination, calculated as the concentration giving a signal equal to three times of the standard deviation of the blank (LOD, 3σblank criterion, peak height) were 3.0, 1.4, 1.5 and 3.8 ng mL- 1 for Hg, As, Sb and Se, respectively. The method was validated by the analysis of three Certified Reference Materials (NIST 2711, NRCC DOLT-2, NIST 1643e) of different matrix composition and by the standard addition technique. The method offers relatively good precision (RSD ranged from 5% to 8%) for microsampling (200 μL) analysis. The measured of contents of elements in certified reference materials were in good agreement with the certified values (Hg 1.99-6.25 μg g- 1, As 16.6-105 μg g- 1, Sb 19.4-56.88 μg g- 1, Se 1.52-11.68 μg g- 1), according to the Student t-test, for a confidence level of 95%.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-02-15

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

  7. Detection of Far-Infrared Water Vapor, Hydroxyl, and Carbon Monoxide Emissions from the Supernova Remnant 3C 391

    CERN Document Server

    Reach, W T; Reach, William T.; Rho, Jeonghee

    1998-01-01

    We report the detection of shock-excited far-infrared emission of H2O, OH, and CO from the supernova remnant 3C 391, using the ISO Long-Wavelength Spectrometer. This is the first detection of thermal H2O and OH emission from a supernova remnant. For two other remnants, W~28 and W~44, CO emission was detected but OH was only detected in absorption. The observed H2O and OH emission lines arise from levels within ~400 K of the ground state, consistent with collisional excitation in warm, dense gas created after the passage of the shock front through the dense clumps in the pre-shock cloud. The post-shock gas we observe has a density ~2x10^5 cm^{-3} and temperature 100-1000 K, and the relative abundances of CO:OH:H2O in the emitting region are 100:1:7 for a temperature of 200 K. The presence of a significant column of warm H2O suggests that the chemistry has been significantly changed by the shock. The existence of significant column densities of both OH and H2O, which is at odds with models for non-dissociative ...

  8. Polycyclic Aromatic Hydrocarbon Emission in Spitzer/IRS Maps. II. A Direct Link between Band Profiles and the Radiation Field Strength

    Science.gov (United States)

    Stock, D. J.; Peeters, E.

    2017-03-01

    We decompose the observed 7.7 μm polycyclic aromatic hydrocarbon (PAH) emission complexes in a large sample of over 7000 mid-infrared spectra of the interstellar medium using spectral cubes observed with the Spitzer/IRS-SL instrument. In order to fit the 7.7 μm PAH emission complex we invoke four Gaussian components, which are found to be very stable in terms of their peak positions and widths across all of our spectra, and subsequently define a decomposition with fixed parameters, which gives an acceptable fit for all the spectra. We see a strong environmental dependence on the interrelationships between our band fluxes—in the H ii regions all four components are intercorrelated, while in the reflection nebulae (RNs) the inner and outer pairs of bands correlate in the same manner as previously seen for NGC 2023. We show that this effect arises because the maps of RNs are dominated by emission from strongly irradiated photodissociation regions, while the much larger maps of H ii regions are dominated by emission from regions much more distant from the exciting stars, leading to subtly different spectral behavior. Further investigation of this dichotomy reveals that the ratio of two of these components (centered at 7.6 and 7.8 μm) is linearly related to the UV-field intensity (log G 0). We find that this relationship does not hold for sources consisting of circumstellar material, which are known to have variable 7.7 μm spectral profiles.

  9. Field measurement of emission factors of PM, EC, OC, parent, nitro-, and oxy- polycyclic aromatic hydrocarbons for residential briquette, coal cake, and wood in rural Shanxi, China.

    Science.gov (United States)

    Shen, Guofeng; Tao, Shu; Wei, Siye; Chen, Yuanchen; Zhang, Yanyan; Shen, Huizhong; Huang, Ye; Zhu, Dan; Yuan, Chenyi; Wang, Haochen; Wang, Yafei; Pei, Lijun; Liao, Yilan; Duan, Yonghong; Wang, Bin; Wang, Rong; Lv, Yan; Li, Wei; Wang, Xilong; Zheng, Xiaoying

    2013-03-19

    Air pollutants from residential solid fuel combustion are attracting growing public concern. Field measured emission factors (EFs) of various air pollutants for solid fuels are close to the reality and urgently needed for better emission estimations. In this study, emission factors of particulate matter (PM), organic carbon (OC), elemental carbon (EC), and various polycyclic aromatic hydrocarbons (PAHs) from residential combustions of coal briquette, coal cake, and wood were measured in rural Heshun County, China. The measured EFs of PM, OC, and EC were 8.1-8.5, 2.2-3.6, 0.91-1.6 g/kg for the wood burnt in a simple metal stove, 0.54-0.64, 0.13-0.14, 0.040-0.0041 g/kg for the briquette burned in an improved stove with a chimney, and 3.2-8.5, 0.38-0.58, 0.022-0.052 g/kg for the homemade coal cake combusted in a brick stove with a flue, respectively. EFs of 28 parent PAHs, 4 oxygenated PAHs, and 9 nitro-PAHs were 182-297, 7.8-10, 0.14-0.55 mg/kg for the wood, 14-16, 1.7-2.6, 0.64-0.83 mg/kg for the briquette, and 168-223, 4.7-9.5, 0.16-2.4 mg/kg for the coal cake, respectively. Emissions from the wood and coal cake combustions were much higher than those for the coal briquette, especially true for high molecular weight PAHs. Most EFs measured in the field were higher than those measured in stove combustions under laboratory conditions.

  10. A Chemical Kinetic Modeling Study of the Effects of Oxygenated Hydrocarbons on Soot Emissions from Diesel Engines

    Energy Technology Data Exchange (ETDEWEB)

    Westbrook, C K; Pitz, W J; Curran, H J

    2005-11-14

    A detailed chemical kinetic modeling approach is used to examine the phenomenon of suppression of sooting in diesel engines by addition of oxygenated hydrocarbon species to the fuel. This suppression, which has been observed experimentally for a few years, is explained kinetically as a reduction in concentrations of soot precursors present in the hot products of a fuel-rich diesel ignition zone when oxygenates are included. Oxygenates decrease the overall equivalence ratio of the igniting mixture, producing higher ignition temperatures and more radical species to consume more soot precursor species, leading to lower soot production. The kinetic model is also used to show how different oxygenates, ester structures in particular, can have different soot-suppression efficiencies due to differences in molecular structure of the oxygenated species.

  11. A Chemical Kinetic Modeling Study of the Effects of Oxygenated Hydrocarbons on Soot Emissions from Diesel Engines

    Energy Technology Data Exchange (ETDEWEB)

    Westbrook, C K; Pitz, W J; Curran, H J

    2005-11-14

    A detailed chemical kinetic modeling approach is used to examine the phenomenon of suppression of sooting in diesel engines by addition of oxygenated hydrocarbon species to the fuel. This suppression, which has been observed experimentally for a few years, is explained kinetically as a reduction in concentrations of soot precursors present in the hot products of a fuel-rich diesel ignition zone when oxygenates are included. Oxygenates decrease the overall equivalence ratio of the igniting mixture, producing higher ignition temperatures and more radical species to consume more soot precursor species, leading to lower soot production. The kinetic model is also used to show how different oxygenates, ester structures in particular, can have different soot-suppression efficiencies due to differences in molecular structure of the oxygenated species.

  12. The vitiation effects of water vapor and carbon dioxide on the autoignition characteristics of kerosene

    Science.gov (United States)

    Liang, Jin-Hu; Wang, Su; Zhang, Sheng-Tao; Yue, Lian-Jie; Fan, Bing-Cheng; Zhang, Xin-Yu; Cui, Ji-Ping

    2014-08-01

    In ground tests of hypersonic scramjet, the high-enthalpy airstream produced by burning hydrocarbon fuels often contains contaminants of water vapor and carbon dioxide. The contaminants may change the ignition characteristics of fuels between ground tests and real flights. In order to properly assess the influence of the contaminants on ignition characteristics of hydrocarbon fuels, the effect of water vapor and carbon dioxide on the ignition delay times of China RP-3 kerosene was studied behind reflected shock waves in a preheated shock tube. Experiments were conducted over a wider temperature range of 800-1 500K, at a pressure of 0.3 MPa, equivalence ratios of 0.5 and 1, and oxygen concentration of 20%. Ignition delay times were determined from the onset of the excited radical OH emission together with the pressure profile. Ignition delay times were measured for four cases: (1) clean gas, (2) gas vitiated with 10% and 20% water vapor in mole, (3) gas vitiated with 10% carbon dioxide in mole, and (4) gas vitiated with 10% water vapor and 10% carbon dioxide, 20% water vapor and 10% carbon dioxide in mole. The results show that carbon dioxide produces an inhibiting effect at temperatures below 1 300 K when ϕ = 0.5, whereas water vapor appears to accelerate the ignition process below a critical temperature of about 1 000 K when ϕ = 0.5. When both water vapor and carbon dioxide exist together, a minor inhibiting effect is observed at ϕ = 0.5, while no effect is found at ϕ = 1.0. The results are also discussed preliminary by considering both the combustion reaction mechanism and the thermophysics properties of the fuel mixtures. The current measurements demonstrate vitiation effects of water vapor and carbon dioxide on the autoignition characteristics of China RP-3 kerosene at air-like O2 concentration. It is important to account for such effects when data are extrapolated from ground testing to real flight conditions.

  13. Environmental dependence of polycyclic aromatic hydrocarbon emission at z~0.8. Investigation by observing the RX J0152.7-1357 with AKARI

    CERN Document Server

    Murata, Kazumi; Tanaka, Masayuki; Matsuhara, Hideo; Kodama, Tadayuki

    2015-01-01

    We study the environmental dependence of the strength of polycyclic aromatic hydrocarbon (PAH) emission by AKARI observations of RX J0152.7-1357, a galaxy cluster at z=0.84. PAH emission reflects the physical conditions of galaxies and dominates 8 um luminosity (L8), which can directly be measured with the L15 band of AKARI. L8 to infrared luminosity (LIR) ratio is used as a tracer of the PAH strength. Both photometric and spectroscopic redshifts are applied to identify the cluster members. The L15-band-detected galaxies tend to reside in the outskirt of the cluster and have optically green colour, R-z'~ 1.2. We find no clear difference of the L8/LIR behaviour of galaxies in field and cluster environment. The L8/LIR of cluster galaxies decreases with specific-star-formation rate divided by that of main-sequence galaxies, and with LIR, consistent with the results for field galaxies. The relation between L8/LIR and LIR is between those at z=0 and z=2 in the literature. Our data also shows that starburst galaxie...

  14. Simultaneous NOx and hydrocarbon emissions control for lean-burn engines using low-temperature solid oxide fuel cell at open circuit.

    Science.gov (United States)

    Huang, Ta-Jen; Hsu, Sheng-Hsiang; Wu, Chung-Ying

    2012-02-21

    The high fuel efficiency of lean-burn engines is associated with high temperature and excess oxygen during combustion and thus is associated with high-concentration NO(x) emission. This work reveals that very high concentration of NO(x) in the exhaust can be reduced and hydrocarbons (HCs) can be simultaneously oxidized using a low-temperature solid oxide fuel cell (SOFC). An SOFC unit is constructed with Ni-YSZ as the anode, YSZ as the electrolyte, and La(0.6)Sr(0.4)CoO(3) (LSC)-Ce(0.9)Gd(0.1)O(1.95) as the cathode, with or without adding vanadium to LSC. SOFC operation at 450 °C and open circuit can effectively treat NO(x) over the cathode at a very high concentration in the simulated exhaust. Higher NO(x) concentration up to 5000 ppm can result in a larger NO(x) to N(2) rate. Moreover, a higher oxygen concentration promotes NO conversion. Complete oxidation of HCs can be achieved by adding silver to the LSC current collecting layer. The SOFC-based emissions control system can treat NO(x) and HCs simultaneously, and can be operated without consuming the anode fuel (a reductant) at near the engine exhaust temperature to eliminate the need for reductant refilling and extra heating.

  15. Emission of polycyclic aromatic hydrocarbons, toxicity, and mutagenicity from domestic cooking using sawdust briquettes, wood, and kerosene.

    Science.gov (United States)

    Kim, OanhNguyenThi; Nghiem, Le Hoang; Phyu, Yin Latt

    2002-03-01

    Smoke samples, in both gas and particulate matter (PM) phases, of the three domestic stoves were collected using U.S. EPA modified method 5 and were analyzed for 17 PAH (HPLC-UV), acute toxicity (Microtox test), and mutagenicity (Amestest). The gas phase of smoke contributed > or = 95% of 17 PAH, > or = 96% of toxicity, and > or = 60% of mutagenicity. The highest emission factor of 17 PAH was from sawdust briquettes (260 mg/kg), but the highest emission of 11 genotoxic PAH was from kerosene (28 mg/kg). PM samples of kerosene smoke were not toxic. The total toxicity emission factor was the highest from sawdust, followed by kerosene and wood fuel. Smoke samples from the kerosene stove were not mutagenic. TA98 indicated the presence of both direct and indirect mutagenic activities in PM samples of sawdust and wood fuel but only direct mutagenic activities in the gas phase. TA100 detected only direct mutagenic activities in both PM and gas-phase samples. The higher mutagenicity emission factor was from wood fuel, 12 x 10(6) revertants/kg (TA100-S9) and 3.5 x 10(6) (TA98-S9), and lower from sawdust, 2.9 x 10(6) (TA100-S9) and 2.8 x 10(6) (TA98-S9). The low burning rate and high efficiency of a kerosene stove have resulted in the lowest PAH, toxicity, and mutagenicity emissions from daily cooking activities. The bioassays produced toxicity and mutagenicity results in correspondence with the PAH content of samples. The tests could be used for a quick assessment of potential health risks.

  16. Synthesis, structural and field emission properties of multiwall carbon nanotube-graphene-like nanocarbon hybrid films grown by microwave plasma enhanced chemical vapor deposition

    Energy Technology Data Exchange (ETDEWEB)

    Chockalingam, Sreekumar, E-mail: sreekuc@nplindia.org [Polymorphic Carbon Thin Films Group, Physics of Energy Harvesting Division, CSIR-National Physical Laboratory, Dr. K. S. Krishnan Marg, New Delhi 110012 (India); Bisht, Atul [Polymorphic Carbon Thin Films Group, Physics of Energy Harvesting Division, CSIR-National Physical Laboratory, Dr. K. S. Krishnan Marg, New Delhi 110012 (India); Panwar, O.S., E-mail: ospanwar@mail.nplindia.ernet.in [Polymorphic Carbon Thin Films Group, Physics of Energy Harvesting Division, CSIR-National Physical Laboratory, Dr. K. S. Krishnan Marg, New Delhi 110012 (India); Kesarwani, A.K. [Polymorphic Carbon Thin Films Group, Physics of Energy Harvesting Division, CSIR-National Physical Laboratory, Dr. K. S. Krishnan Marg, New Delhi 110012 (India); Singh, B.P. [Physics and Engineering of Carbon, Materials Physics and Engineering Division, CSIR-National Physical Laboratory, Dr. K. S. Krishnan Marg, New Delhi 110012 (India); Chand, Jagdish [Polymorphic Carbon Thin Films Group, Physics of Energy Harvesting Division, CSIR-National Physical Laboratory, Dr. K. S. Krishnan Marg, New Delhi 110012 (India); Singh, V.N. [Electron and Ion Microscopy, Sophisticated and Analytical Instruments, CSIR-National Physical Laboratory, Dr. K. S. Krishnan Marg, New Delhi 110012 (India)

    2015-04-15

    Multiwall carbon nanotube (MWCNT)-graphene-like nanocarbon hybrid films were directly deposited on nickel substrate without any pre-treatment in a single-step by microwave plasma enhanced chemical vapor deposition (MW PECVD) technique at 600 °C. The effects of hydrogen partial pressure on the growth of MWCNT-graphene-like nanocarbon hybrid films and their structural, morphological and field emission properties were investigated. High resolution scanning electron microscope revealed MWCNT structure. High resolution transmission electron microscope images and Raman spectra revealed graphene-like nanocarbon film. Raman spectra showed 2D, G, D and D + G peaks at approximately 2690, 1590, 1350 and 2930 cm{sup −1}, respectively. The minimum threshold field for electron emission was found to be 3.6 V/μm corresponding to 1 μA/cm{sup 2} current density for the MWCNT-graphene-like nanocarbon hybrid film deposited at 20 Torr pressure whereas the maximum current density of 0.12 mA/cm{sup 2} and field enhancement factor of ∼3356 was obtained for the sample deposited at 5 Torr pressure. - Highlights: • MWCNT-graphene-like nanocarbon hybrid films were synthesized by MWPECVD technique. • Effect of pressure on the structural and field emission properties has been studied. • FESEM revealed MWCNT and HRTEM revealed graphene-like nanocarbon film structure. • Minimum E{sub T} = 3.6 V/μm with β = 3164 has been obtained in the film deposited at 20 Torr. • Maximum J = 0.12 mA/cm{sup 2} with β = 3356 has been obtained in the film deposited at 5 Torr.

  17. Attributing risk burden of PM2.5-bound polycyclic aromatic hydrocarbons to major emission sources: Case study in Guangzhou, south China

    Science.gov (United States)

    Yu, Qingqing; Gao, Bo; Li, Guanghui; Zhang, Yanli; He, Quanfu; Deng, Wei; Huang, Zhonghui; Ding, Xiang; Hu, Qihou; Huang, Zuzhao; Wang, Yujun; Bi, Xinhui; Wang, Xinming

    2016-10-01

    Polycyclic aromatic hydrocarbons (PAHs) have attracted an increasing concern in China's megacities. However, rare information is available on the spatial and seasonal variations of inhalation cancer risk (ICR) due to PAH exposure and their relations to specific sources. In this study, year-round PM2.5 samples were collected from 2013 to 2014 by high-volume samplers at four sites (one urban, two rural and one roadside station) in Guangzhou in the highly industrialized and densely populated Pearl River Delta (PRD) region and analyzed for 26 polycyclic aromatic hydrocarbons (PAHs) together with molecular tracers including levoglucosan, hopanes and elemental carbon. Higher molecular weight PAHs (5-ring or above) accounted for 64.3-87.5% of total PAHs. Estimated annual averages of benzo(a)pyrene-equivalent carcinogenic potency (BaPeq) were 1.37, 2.31 and 1.56 ng/m3 at urban SZ, rural JL and rural WQS, respectively, much higher than that at the roadside station YJ in an urban street canyon. ICR of PAHs in wintertime reached 2.2 × 10-4, nearly 3 times that in summer; and cancer risk of PAHs was surprisingly higher at the rural site than at other sites. Source contributions by positive matrix factorization (PMF) in the aid of molecular tracers revealed that overall coal combustion and biomass burning altogether contributed 73.8% of total PAHs and 85.2% of BaPeq, and particularly in winter biomass burning became the most significant source of total PAHs and BaPeq (51.8% and 52.5%), followed by coal combustion (32.0% and 39.1%) and vehicle emission (16.2% and 8.4%). The findings of this work suggest that even in China's megacities like Guangzhou, limiting biomass burning may benefit PAHs pollution control and cancer risk reduction.

  18. On-road traffic emissions of polycyclic aromatic hydrocarbons and their oxy- and nitro- derivative compounds measured in road tunnel environments.

    Science.gov (United States)

    Keyte, Ian J; Albinet, Alexandre; Harrison, Roy M

    2016-10-01

    Vehicular emissions are a key source of polycyclic aromatic compounds (PACs), including polycyclic aromatic hydrocarbons (PAHs) and their oxygenated (OPAH) and nitrated (NPAH) derivatives, in the urban environment. Road tunnels are a useful environment for the characterisation of on-road vehicular emissions, providing a realistic traffic fleet and a lack of direct sunlight, chemical reactivity and non-traffic sources. In the present investigation the concentrations of selected PAHs, OPAHs and NPAHs have been measured in the Parc des Princes Tunnel in Paris (PdPT, France), and at the Queensway Road Tunnel and an urban background site in Birmingham (QT, U.K). A higher proportion of semi-volatile (3-4 ring) PAH, OPAH and NPAH compounds are associated with the particulate phase compared with samples from the ambient environment. A large (~85%) decline in total PAH concentrations is observed between 1992 and 2012 measurements in QT. This is attributed primarily to the introduction of catalytic converters in the U.K as well as increasingly stringent EU vehicle emissions legislation. In contrast, NPAH concentrations measured in 2012 are similar to those measured in 1996. This observation, in addition to an increased proportion of (Phe+Flt+Pyr) in the observed PAH burden in the tunnel, is attributed to the increased number of diesel passenger vehicles in the U.K during this period. Except for OPAHs, comparable PAH and NPAH concentrations are observed in both investigated tunnels (QT and PdP). Significant differences are shown for specific substances between PAC chemical profiles in relation with the national traffic fleet differences (33% diesel passenger cars in U.K. vs 69% in France and up to 80% taking into account all vehicle categories). The dominating and sole contribution of 1-Nitropyrene observed in the PdPT NPAH profile strengthens the promising use of this compound as a diesel exhaust marker for PM source apportionment studies.

  19. Investigations of the causes of hydrocarbon emissions in spark ignition engines with homogeneous charge compression ignition (HCCI). A report of the Institute for Internal Combustion Engines and Automotive Engineering, TU Vienna (IVK); Untersuchung der Ursachen fuer Kohlenwasserstoff-Emissionen beim Ottomotor mit homogener Selbstzuendung (HCCI). Bericht des Instituts fuer Verbrennungskraftmaschinen und Kraftfahrzeugbau derTechnischen Universitaet Wien (IVK)

    Energy Technology Data Exchange (ETDEWEB)

    Geringer, B. (ed.) [Technische Univ., Vienna (Austria); Loch, A.

    2007-07-01

    The main aim of research and development in the field of internal combustion engine is to create an engine with low fuel consumption and hence low carbon dioxide emissions to meet future emissions regulations as well as providing a good driving experience. Homogeneous charge compression ignition (HCCI) is an alternative combustion process being currently developed that promises a good fuel consumption rate and low nitrogen oxide emissions for the gasoline engine. The only legally restricted exhaust gas emissions for this combustion process are carbon monoxide (CO) and hydrocarbons (HC). The aim of this research was a better understanding of the causes and sources of hydrocarbon emissions with HCCI using gasoline so as to further reduce hydrocarbon emissions. A description of the HCCI combustion process is followed by a list of the known sources of hydrocarbon emission in conventional gasoline engines and current knowledge of the causes of hydrocarbon emission with HCCI. It is assumed that many of the known causes of hydrocarbon emissions in the conventional gasoline combustion process are the same for HCCI. For this reason, this study focused on combustion and carburation, which is where the combustion processes differ the most. (orig.)

  20. Vapor recovery system in the gasolines commercialization; Sistema de recuperacion de vapores en la comercializacion de las gasolinas

    Energy Technology Data Exchange (ETDEWEB)

    Casas Barba, R.; Molina Gallegos, J.R. [Instituto Mexicano del Petroleo (IMP), Mexico, D. F. (Mexico)

    1995-12-31

    In the last years the studies performed with respect to the environmental pollution show that the ozone is one of the most problematic contaminants in the Metropolitan Zone of Mexico City (MZMC) and that the hydrocarbons are the main forerunners of it. The main source of hydrocarbon vapor emissions originates from the handling and distribution operations. In this paper a description is made of the involved stages in the commercialization of gasolines in the MZMC and a description is also made of the systems employed to control the emissions in the three stages of the fuels storage and distribution cycle and explains the degree the hydrocarbon emissions to the atmosphere will be reduced, once the recovery systems are installed in all of the involved stages. [Espanol] En los ultimos anos los estudios realizados con respecto a contaminacion ambiental reflejan que el ozono es uno de los contaminantes mas problematicos de la zona metropolitana de la ciudad de Mexico (ZMCM), y los hidrocarburos son los principales precursores de este. La principal fuente de emision de vapores de hidrocarburos proviene de las operaciones de manejo y distribucion de combustibles. En este articulo se hace una descripcion de las etapas involucradas en la comercializacion de las gasolinas en la ZMCM, se describen tambien los sistemas utilizados para controlar las emisiones en las tres etapas del ciclo de almacenamiento y distribucion de combustibles y se explica en que grado se reduciran las emisiones de hidrocarburos a la atmosfera, una vez que se instalen los sistemas de recuperacion en todas las etapas involucradas.

  1. Hotspot of glyoxal over the Pearl River delta seen from the OMI satellite instrument: implications for emissions of aromatic hydrocarbons

    Science.gov (United States)

    Miller, Christopher Chan; Jacob, Daniel J.; González Abad, Gonzalo; Chance, Kelly

    2016-04-01

    The Pearl River delta (PRD) is a densely populated hub of industrial activity located in southern China. OMI (Ozone Monitoring Instrument) satellite observations reveal a large hotspot of glyoxal (CHOCHO) over the PRD that is almost twice as large as any other in Asia. Formaldehyde (HCHO) and NO2 observed by OMI are also high in the PRD but no more than in other urban/industrial areas of China. The CHOCHO hotspot over the PRD can be explained by industrial paint and solvent emissions of aromatic volatile organic compounds (VOCs), with toluene being a dominant contributor. By contrast, HCHO in the PRD originates mostly from VOCs emitted by combustion (principally vehicles). By applying a plume transport model to wind-segregated OMI data, we show that the CHOCHO and HCHO enhancements over the PRD observed by OMI are consistent with current VOC emission inventories. Prior work using CHOCHO retrievals from the SCIAMACHY satellite instrument suggested that emission inventories for aromatic VOCs in the PRD were too low by a factor of 10-20; we attribute this result in part to bias in the SCIAMACHY data and in part to underestimated CHOCHO yields from oxidation of aromatics. Our work points to the importance of better understanding CHOCHO yields from the oxidation of aromatics in order to interpret space-based CHOCHO observations in polluted environments.

  2. How consistent are top-down hydrocarbon emissions based on formaldehyde observations from GOME-2 and OMI?

    Science.gov (United States)

    Stavrakou, T.; Müller, J.-F.; Bauwens, M.; De Smedt, I.; Van Roozendael, M.; De Mazière, M.; Vigouroux, C.; Hendrick, F.; George, M.; Clerbaux, C.; Coheur, P.-F.; Guenther, A.

    2015-10-01

    The vertical columns of formaldehyde (HCHO) retrieved from two satellite instruments, the Global Ozone Monitoring Instrument-2 (GOME-2) on Metop-A and the Ozone Monitoring Instrument (OMI) on Aura, are used to constrain global emissions of HCHO precursors from open fires, vegetation and human activities in the year 2010. To this end, the emissions are varied and optimized using the adjoint model technique in the IMAGESv2 global CTM (chemical transport model) on a monthly basis and at the model resolution. Given the different local overpass times of GOME-2 (09:30 LT) and OMI (13:30 LT), the simulated diurnal cycle of HCHO columns is investigated and evaluated against ground-based optical measurements at seven sites in Europe, China and Africa. The modeled diurnal cycle exhibits large variability, reflecting competition between photochemistry and emission variations, with noon or early afternoon maxima at remote locations (oceans) and in regions dominated by anthropogenic emissions, late afternoon or evening maxima over fire scenes, and midday minima in isoprene-rich regions. The agreement between simulated and ground-based columns is generally better in summer (with a clear afternoon maximum at mid-latitude sites) than in winter, and the annually averaged ratio of afternoon to morning columns is slightly higher in the model (1.126) than in the ground-based measurements (1.043). The anthropogenic VOC (volatile organic compound) sources are found to be weakly constrained by the inversions on the global scale, mainly owing to their generally minor contribution to the HCHO columns, except over strongly polluted regions, like China. The OMI-based inversion yields total flux estimates over China close to the bottom-up inventory (24.6 vs. 25.5 TgVOC yr-1 in the a priori) with, however, pronounced increases in the northeast of China and reductions in the south. Lower fluxes are estimated based on GOME-2 HCHO columns (20.6 TgVOC yr-1), in particular over the northeast

  3. How consistent are top-down hydrocarbon emissions based on formaldehyde observations from GOME-2 and OMI?

    Directory of Open Access Journals (Sweden)

    T. Stavrakou

    2015-04-01

    Full Text Available The vertical columns of formaldehyde (HCHO retrieved from two satellite instruments, the Global Ozone Monitoring Instrument-2 (GOME-2 on Metop-A and the Ozone Monitoring Instrument (OMI on Aura, are used to constrain global emissions of HCHO precursors from open fires, vegetation and human activities in the year 2010. To this end, the emissions are varied and optimized using the adjoint model technique in the IMAGESv2 global CTM (chemistry-transport model on a monthly basis and at the model resolution. Given the different local overpass times of GOME-2 (09:30 LT and OMI (13:30 LT, the simulated diurnal cycle of HCHO columns is investigated and evaluated against ground-based optical measurements at 7 sites in Europe, China and Africa. The modelled diurnal cycle exhibits large variability, reflecting competition between photochemistry and emission variations, with noon or early afternoon maxima at remote locations (oceans and in regions dominated by anthropogenic emissions, late afternoon or evening maxima over fire scenes, and midday minima in isoprene-rich regions. The agreement between simulated and ground-based columns is found to be generally better in summer (with a clear afternoon maximum at mid-latitude sites than in winter, and the annually averaged ratio of afternoon to morning columns is slightly higher in the model (1.126 than in the ground-based measurements (1.043. The anthropogenic VOC (volatile organic compound sources are found to be weakly constrained by the inversions on the global scale, mainly owing to their generally minor contribution to the HCHO columns, except over strongly polluted regions, like China. The OMI-based inversion yields total flux estimates over China close to the bottom-up inventory (24.6 vs. 25.5 in the a priori with, however, pronounced increases in the Northeast China and reductions in the south. Lower fluxes are estimated based on GOME-2 HCHO columns (20.6 TgVOC, in particular over the Northeast, likely

  4. Sub-band gap photo-enhanced secondary electron emission from high-purity single-crystal chemical-vapor-deposited diamond

    Science.gov (United States)

    Yater, J. E.; Shaw, J. L.; Pate, B. B.; Feygelson, T. I.

    2016-02-01

    Secondary-electron-emission (SEE) current measured from high-purity, single-crystal (100) chemical-vapor-deposited diamond is found to increase when sub-band gap (3.06 eV) photons are incident on the hydrogenated surface. Although the light does not produce photoemission directly, the SEE current increases by more than a factor of 2 before saturating with increasing laser power. In energy distribution curves (EDCs), the emission peak shows a corresponding increase in intensity with increasing laser power. However, the emission-onset energy in the EDCs remains constant, indicating that the bands are pinned at the surface. On the other hand, changes are observed on the high-energy side of the distribution as the laser power increases, with a well-defined shoulder becoming more pronounced. From an analysis of this feature in the EDCs, it is deduced that upward band bending is present in the near-surface region during the SEE measurements and this band bending suppresses the SEE yield. However, sub-band gap photon illumination reduces the band bending and thereby increases the SEE current. Because the bands are pinned at the surface, we conclude that the changes in the band levels occur below the surface in the electron transport region. Sample heating produces similar effects as observed with sub-band gap photon illumination, namely, an increase in SEE current and a reduction in band bending. However, the upward band bending is not fully removed by either increasing laser power or temperature, and a minimum band bending of ˜0.8 eV is established in both cases. The sub-band gap photo-excitation mechanism is under further investigation, although it appears likely at present that defect or gap states play a role in the photo-enhanced SEE process. In the meantime, the study demonstrates the ability of visible light to modify the electronic properties of diamond and enhance the emission capabilities, which may have potential impact for diamond-based vacuum electron

  5. How consistent are top-down hydrocarbon emissions based on formaldehyde observations from GOME-2 and OMI?

    Energy Technology Data Exchange (ETDEWEB)

    Stavrakou, T. [Belgium Inst. for Space Aeronomy, Brussels (Belgium); Muller, J. F. [Belgium Inst. for Space Aeronomy, Brussels (Belgium); Bauwens, M. [Belgium Inst. for Space Aeronomy, Brussels (Belgium); De Smedt, I. [Belgium Inst. for Space Aeronomy, Brussels (Belgium); Van Roozendael, M. [Belgium Inst. for Space Aeronomy, Brussels (Belgium); De Maziere, M. [Belgium Inst. for Space Aeronomy, Brussels (Belgium); Vigouroux, C. [Belgium Inst. for Space Aeronomy, Brussels (Belgium); Hendrick, F. [Belgium Inst. for Space Aeronomy, Brussels (Belgium); George, M. [UPMC Univ., Paris (France); Clerbaux, C. [UPMC Univ., Paris (France); Free University of Brussels (Germany); Coheur, P-F [Free University of Brussels (Germany); Guenther, Alex B. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2015-10-26

    The vertical columns of formaldehyde (HCHO) retrieved from two satellite instruments, the Global Ozone Monitoring Instrument-2 (GOME-2) on Metop-A and the Ozone Monitoring Instrument (OMI) on Aura, are used to constrain global emissions of HCHO precursors from open fires, vegetation and human activities in the year 2010. To this end, the emissions are varied and optimized using the ad-joint model technique in the IMAGESv2 global CTM (chem-ical transport model) on a monthly basis and at the model res-olution. Given the different local overpass times of GOME- 2 (09:30 LT) and OMI (13:30 LT), the simulated diurnal cy-cle of HCHO columns is investigated and evaluated against ground-based optical measurements at seven sites in Europe, China and Africa. The modeled diurnal cycle exhibits large variability, reflecting competition between photochemistry and emission variations, with noon or early afternoon max-ima at remote locations (oceans) and in regions dominated by anthropogenic emissions, late afternoon or evening max-ima over fire scenes, and midday minima in isoprene-rich re-gions. The agreement between simulated and ground-based columns is generally better in summer (with a clear after-noon maximum at mid-latitude sites) than in winter, and the annually averaged ratio of afternoon to morning columns is slightly higher in the model (1.126) than in the ground-based measurements (1.043).The anthropogenic VOC (volatile organic compound) sources are found to be weakly constrained by the inversions on the global scale, mainly owing to their generally minor contribution to the HCHO columns, except over strongly pol-luted regions, like China. The OMI-based inversion yields total flux estimates over China close to the bottom-up inven-tory (24.6 vs. 25.5 TgVOC yr-1 in the a priori) with, how-ever, pronounced increases in the northeast of China and re-ductions in the south. Lower fluxes are estimated based on GOME-2 HCHO columns (20.6 TgVOC yr-1), in

  6. Nanocrystalline Si/SiO{sub 2} core-shell network with intense white light emission fabricated by hot-wire chemical vapor deposition

    Energy Technology Data Exchange (ETDEWEB)

    Matsumoto, Y., E-mail: ymatsumo@cinvestav.mx; Dutt, A. [SEES, Electrical Engineering Department, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Cinvestav-IPN, Mexico, D.F. 07360 (Mexico); Santana-Rodríguez, G. [Institute of Material Research, Universidad Nacional Autónoma de México, Coyoacán 04510 (Mexico); Santoyo-Salazar, J. [Department of Physics, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Cinvestav-IPN, Mexico, D.F. 07360 (Mexico); Aceves-Mijares, M. [Departament of Electronics, Instituto Nacional de Astrofísica Óptica y Electrónica, Tonantzintla, Puebla 72000 (Mexico)

    2015-04-27

    We report the fabrication of a stable Si/SiO{sub 2} core-shell network using hot-wire chemical vapor deposition on a silicon substrate at a relatively low substrate temperature of 200 °C. Structural investigations using transmission electron microscopy and X-ray diffraction confirm the presence of nanocrystalline silicon and silicon dioxide quantum dots in the form of a core-shell network embedded in the amorphous SiO{sub x} matrix, while selected area electron diffraction confirms the formation of a core-shell structure. The core-shell structure exhibits a bright white emission that can be seen with the unaided eye at room temperature without any post-annealing treatments, and the observed photoemission does not alter in color or intensity after prolonged laser exposure. Additional measurements are performed while varying the laser power and optical gain is found in the as-deposited material. Intense stable white luminescence is observed and shows the prospective for various optical and biological applications in the future.

  7. Nanocrystalline Si/SiO2 core-shell network with intense white light emission fabricated by hot-wire chemical vapor deposition

    Science.gov (United States)

    Matsumoto, Y.; Dutt, A.; Santana-Rodríguez, G.; Santoyo-Salazar, J.; Aceves-Mijares, M.

    2015-04-01

    We report the fabrication of a stable Si/SiO2 core-shell network using hot-wire chemical vapor deposition on a silicon substrate at a relatively low substrate temperature of 200 °C. Structural investigations using transmission electron microscopy and X-ray diffraction confirm the presence of nanocrystalline silicon and silicon dioxide quantum dots in the form of a core-shell network embedded in the amorphous SiOx matrix, while selected area electron diffraction confirms the formation of a core-shell structure. The core-shell structure exhibits a bright white emission that can be seen with the unaided eye at room temperature without any post-annealing treatments, and the observed photoemission does not alter in color or intensity after prolonged laser exposure. Additional measurements are performed while varying the laser power and optical gain is found in the as-deposited material. Intense stable white luminescence is observed and shows the prospective for various optical and biological applications in the future.

  8. Long-Term Hydrocarbon Trade Options for the Maghreb Region and Europe—Renewable Energy Based Synthetic Fuels for a Net Zero Emissions World

    Directory of Open Access Journals (Sweden)

    Mahdi Fasihi

    2017-02-01

    Full Text Available Concerns about climate change and increasing emission costs are drivers for new sources of fuels for Europe. Sustainable hydrocarbons can be produced synthetically by power-to-gas (PtG and power-to-liquids (PtL facilities, for sectors with low direct electrification such as aviation, heavy transportation and chemical industry. Hybrid PV–Wind power plants can harvest high solar and wind potentials of the Maghreb region to power these systems. This paper calculates the cost of these fuels for Europe, and presents a respective business case for the Maghreb region. Calculations are hourly resolved to find the least cost combination of technologies in a 0.45° × 0.45° spatial resolution. Results show that, for 7% weighted average cost of capital (WACC, renewable energy based synthetic natural gas (RE-SNG and RE-diesel can be produced in 2030 for a minimum cost of 76 €/MWhHHV (0.78 €/m3SNG and 88 €/MWhHHV (0.85 €/L, respectively. While in 2040, these production costs can drop to 66 €/MWhHHV (0.68 €/m3SNG and 83 €/MWhHHV (0.80 €/L, respectively. Considering access to a WACC of 5% in a de-risking project, oxygen sales and CO2 emissions costs, RE-diesel can reach fuel-parity at crude oil prices of 101 and 83 USD/bbl in 2030 and 2040, respectively. Thus, RE-synthetic fuels could be produced to answer fuel demand and remove environmental concerns in Europe at an affordable cost.

  9. Comparison of the Emission of Aromatic Hydrocarbons from Moulding Sands with Furfural Resin with the Low Content of Furfuryl Alcohol and Different Activators

    Directory of Open Access Journals (Sweden)

    Żymankowska-Kumon S.

    2016-12-01

    Full Text Available No-bake process refers to the use of chemical binders to bond the moulding sand. Sand is moved to the mould fill station in preparation for filling of the mould. A mixer is used to blend the sand with the chemical binder and activator. As the sand exits the mixer, the binder begins the chemical process of hardening. This paper presents the results of decomposition of the moulding sands with modified urea-furfuryl resin (with the low content of furfuryl alcohol below 25 % and different activators: organic and inorganic on a quartz matrix, under semi-industrial conditions. Investigations of the gases emission in the test foundry plant were executed according to the method extended in the Faculty of Foundry Engineering (AGH University of Science and Technology. Article presents the results of the emitted chosen aromatic hydrocarbons and loss on ignition compared with the different activators used to harden this resin. On the bases of the data, it is possible to determine the content of the emitted dangerous substances from the moulding sand according to the content of loss on ignition.

  10. Chemometrics-assisted excitation-emission fluorescence spectroscopy on nylon-attached rotating disks. Simultaneous determination of polycyclic aromatic hydrocarbons in the presence of interferences.

    Science.gov (United States)

    Cañas, Alejandro; Richter, Pablo; Escandar, Graciela M

    2014-12-10

    This work presents a green and very simple approach which enables the accurate and simultaneous determination of benzo[a]pyrene, dibenz[a,h]anthracene, benz[a]anthracene, and chrysene, concerned and potentially carcinogenic heavy-polycyclic aromatic hydrocarbons (PAHs) in interfering samples. The compounds are extracted from water samples onto a device composed of a small rotating Teflon disk, with a nylon membrane attached to one of its surfaces. After extraction, the nylon membrane containing the concentrated analytes is separated from the Teflon disk, and fluorescence excitation-emission matrices are directly measured on the nylon surface, and processed by applying parallel factor analysis (PARAFAC), without the necessity of a desorption step. Under optimum conditions and for a sample volume of 25 mL, the PAHs extraction was carried out in 20 min. Detection limits based on the IUPAC recommended criterion and relative errors of prediction were in the ranges 20-100 ng L(-1) and 5-7%, respectively. Thanks to the combination of the ability of nylon to strongly retain PAHs, the easy rotating disk extraction approach, and the selectivity of second-order calibration, which greatly simplifies sample treatment avoiding the use of toxic solvents, the developed method follows most green analytical chemistry principles.

  11. Hydrocarbon raw emission characterization of a direct-injection spark ignition engine operated with alcohol and furan-based bio fuels

    Energy Technology Data Exchange (ETDEWEB)

    Thewes, Matthias [FEV GmbH, Aachen (Germany); Mauermann, Peter; Pischinger, Stefan [RWTH Aachen Univ. (Germany). Inst. for Combustion Engines; Bluhm, Kerstin; Hollert, Henner [RWTH Aachen Univ. (Germany). Inst. for Environmental Research, Dept. of Ecosystem Analysis

    2013-06-01

    Within the Cluster of Excellence ''Tailor-Made Fuels from Biomass'' the impact of various potential bio fuels on engine combustion is studied. Besides alcohols, furan-based bio fuels have come into the focus with novel production routes to transform biomass into 2-Methylfuran or 2,5-Dimethylfuran. In the present study, the influence of these and other bio fuels on the hydrocarbon raw emission spectrum of a direct-injection spark-ignition single cylinder engine is studied experimentally by means of gas chromatographic and mass spectroscopic analysis of exhaust gas samples. The results obtained are compared to operation with conventional EN 228 gasoline fuel. This fuel showed slip of partially carcinogenic aromatic fuel molecule(s) in warm and in cold engine conditions. For the bio fuels, slip was found to be significant for the alcohol fuels. The carcinogenic molecule 1,3-Butadiene was present in the exhaust gas of all fuels. Furan as another possibly carcinogenic molecule was found at significantly higher concentrations in the exhaust gas of the furan-based bio fuels compared to conventional gasoline fuel but not in the exhaust gas of the alcohol fuels. (orig.)

  12. A low-order model of water vapor, clouds, and thermal emission for tidally locked terrestrial planets

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Jun; Abbot, Dorian S., E-mail: junyang28@uchicago.edu [Department of the Geophysical Sciences, University of Chicago, 5734 South Ellis Avenue, Chicago, IL 60637 (United States)

    2014-04-01

    In the spirit of minimal modeling of complex systems, we develop an idealized two-column model to investigate the climate of tidally locked terrestrial planets with Earth-like atmospheres in the habitable zone of M-dwarf stars. The model is able to approximate the fundamental features of the climate obtained from three-dimensional (3D) atmospheric general circulation model (GCM) simulations. One important reason for the two-column model's success is that it reproduces the high cloud albedo of the GCM simulations, which reduces the planet's temperature and delays the onset of a runaway greenhouse state. The two-column model also clearly illustrates a secondary mechanism for determining the climate: the nightside acts as a 'radiator fin' through which infrared energy can be lost to space easily. This radiator fin is maintained by a temperature inversion and dry air on the nightside, and plays a similar role to the subtropics on modern Earth. Since one-dimensional radiative-convective models cannot capture the effects of the cloud albedo and radiator fin, they are systematically biased toward a narrower habitable zone. We also show that cloud parameters are the most important in the two-column model for determining the day-night thermal emission contrast, which decreases and eventually reverses as the stellar flux increases. This reversal is important because it could be detected by future extrasolar planet characterization missions, which would suggest that the planet has Earth-like water clouds and is potentially habitable.

  13. 40 CFR 86.317-79 - Hydrocarbon analyzer specifications.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 18 2010-07-01 2010-07-01 false Hydrocarbon analyzer specifications....317-79 Hydrocarbon analyzer specifications. (a) Hydrocarbon measurements are to be made with a heated... measures hydrocarbon emissions on a dry basis is permitted for gasoline-fueled testing; Provided,...

  14. On-line cloud point extraction combined with electrothermal vaporization inductively coupled plasma atomic emission spectrometry for the speciation of inorganic antimony in environmental and biological samples

    Energy Technology Data Exchange (ETDEWEB)

    Li Yingjie [Department of Chemistry, Wuhan University, Wuhan 430072 (China); Hu Bin [Department of Chemistry, Wuhan University, Wuhan 430072 (China)]. E-mail: binhu@whu.edu.cn; Jiang Zucheng [Department of Chemistry, Wuhan University, Wuhan 430072 (China)

    2006-08-25

    A new method for the determination of inorganic Sb species by on-line cloud point extraction combined with electrothermal vaporization inductively coupled plasma atomic emission spectrometry (ETV-ICP-AES) is presented and evaluated. The method is based on the complexation of Sb(III) with pyrrolidine dithiocarbamate (PDC) which form an hydrophobic complex at pH 5.5 and subsequently enter surfactant-rich phase at pH 5.5, whereas Sb(V) remained in aqueous solutions. The preconcentration step is mediated by micelles of the non-ionic surfactant Triton X-114 with ammonium pyrrolidine dithiocarbamate (APDC). The micellar system containing the complex was loaded into the FIA manifold at a flow rate of 2.5 mL min{sup -1}, and the surfactant-rich phase was retained in a microcolumn packed with absorbent cotton, at pH 5.5. After the surfactant-rich phase was eluted with 100 {mu}L acetonitrile, it was determined by ETV-ICP-AES. Sb(V) is reduced to Sb(III) by L-cysteine prior to determined total Sb, and its assay is based on subtracting Sb(III) from total antimony. The main factors affecting separation/preconcentration and the vaporization behavior of analyte in graphite tube were investigated in detail. Under the optimized conditions, the precision relative standard deviation (R.S.D.) for eight replicate measurements of 0.2 {mu}g mL{sup -1} Sb(III) was 4.3%. The apparent concentration factor, which is defined as the concentration ratio of the analyte in the final diluted surfactant-rich extract ready for ETV-ICP-AES detection and in the initial solution, was 872 for Sb(III). The limit of detection (LOD) for Sb(III) was 0.09 {mu}g L{sup -1}. The proposed method was successfully applied for the speciation of inorganic antimony in different water samples and urine sample with satisfactory results.

  15. Characterization of polycyclic aromatic hydrocarbons in fugitive PM10 emissions from an integrated iron and steel plant.

    Science.gov (United States)

    Khaparde, V V; Bhanarkar, A D; Majumdar, Deepanjan; Rao, C V Chalapati

    2016-08-15

    Fugitive emissions of PM10 (particles blast furnace and steel manufacturing unit in an integrated iron and steel plant situated in India. Concentrations of PM10, PM10-bound total PAHs, benzo (a) pyrene, carcinogenic PAHs and combustion PAHs were found to be highest around the sintering unit. Concentrations of 3-ring and 4-ring PAHs were recorded to be highest in the coking unit whereas 5-and 6-ring PAHs were found to be highest in other units. The following indicatory PAHs were identified: indeno (1,2,3-cd) pyrene, dibenzo (a,h) anthracene, benzo (k) fluoranthene in blast furnace unit; indeno (1,2,3-cd) pyrene, dibenzo (a,h) anthracene, chrysene in sintering unit; Anthracene, fluoranthene, chrysene in coking unit and acenaphthene, fluoranthene, fluorene in steel making unit. Total-BaP-TEQ (Total BaP toxic equivalent quotient) and BaP-MEQ (Total BaP mutagenic equivalent quotient) concentration levels ranged from 2.4 to 231.7ng/m(3) and 1.9 to 175.8ng/m(3), respectively. BaP and DbA (dibenzo (a,h) anthracene) contribution to total-BaP-TEQ was found to be the highest.

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

    Directory of Open Access Journals (Sweden)

    L. Poulain

    2011-12-01

    Full Text Available Residential wood burning is becoming an increasingly important cause of air quality problems since it has become a popular source of alternative energy to fossil fuel. In order to characterize the contribution of residential wood burning to local particle pollution, a field campaign was organized at the village of Seiffen (Saxony, Germany. During this campaign, an Aerosol Mass Spectrometer (AMS was deployed in parallel to a PM1 high volume filter sampler. The AMS mass spectra were analyzed using Positive Matrix Factorization (PMF to obtain detailed information about the organic aerosol (OA. Biomass-burning organic aerosol (BBOA, Hydrocarbon-like organic aerosol (HOA, and Oxygenated Organic Aerosol (OOA were identified and represented 20%, 17% and 62% of total OA, respectively. Additionally, Polycyclic Aromatic Hydrocarbons (PAH were measured by the AMS with an average concentration of 10 ng m−3 and short term events of extremely high PAH concentration (up to 500 ng m−3 compared to the mean PAH value were observed during the whole measurement period. A comparison with the results from PM1 filter samples showed that the BBOA factor and the AMS PAH are good indicators of the total concentration of the different monosaccharide anhydrides and PAH measured on the filter samples. Based on its low correlation with CO and the low car traffic, the HOA factor was considered to be related to residential heating using liquid fuel. An influence of the time of the week (week vs. weekend on the diurnal profiles of the different OA components was observed. The weekdays were characterized by two maxima; a first one early in the morning and a stronger one in the evening. During the weekend days, the different OA components principally reached only one maximum in the afternoon. Finally, the PAH emitted directly from residential wood combustion was estimated to represent 1.5% of the total mass of the BBOA factor and

  17. Nonmethane hydrocarbon and oxy hydrocarbon measurements during the 2002 New England Air Quality Study

    Science.gov (United States)

    Goldan, Paul D.; Kuster, William C.; Williams, Eric; Murphy, Paul C.; Fehsenfeld, Fred C.; Meagher, James

    2004-11-01

    Nonmethane hydrocarbons (NMHCs) and oxy hydrocarbons (oxy HCs) were measured aboard the National Oceanic and Atmospheric Administration research vessel Ronald H. Brown during the New England Air Quality Study from 13 July to 10 August 2002 by an online dual gas chromatographic instrument with two separate analytical columns equipped, respectively, with flame ionization and mass spectrometer detectors. Measurements, taken each half hour, included C2 to C10 alkanes, C2 to C5 alkenes, alcohols and ketones, C6 to C9 aromatics, and biogenic volatile compounds including six monoterpenes, isoprene and its immediate oxidation products methacrolein and methylvinylketone. All compounds have been categorized by their contribution to the OH loss rate calculated for 298K and 1 atm. Large temporal variability was observed for all compounds. Airflow from the Providence, Rhode Island/Boston, Massachusetts, urban corridor northeast to the New Hampshire coast was usually heavily laden with NMHCs and oxy HCs of anthropogenic origin. Comparison of specific compound ratios with automotive tunnel studies suggested that these were predominantly mobile source emissions. When such flow occurred during daylight hours, these urban plumes were accompanied by increases in ozone in the 80 to 120 ppbv range. About equally as often, much less chemically mature NMHC plumes were encountered near the New Hampshire coast. Ozone was titrated out of these latter plumes, and the unusually high mixing ratios of C4 and C5 alkenes suggested that their source was partly gasoline vapor release rather than mobile source emissions. In the New England coastal region explored, in spite of the large anthropogenic NMHC input during periods of offshore flow, OH loss with hydrocarbons was frequently dominated by compounds of biogenic origin. During periods of cleaner marine air inflow the OH loss rate was dominated by reaction with methane and with oxy HCs, predominantly acetone, formaldehyde, and acetaldehyde.

  18. Particulate Emissions Hazards Associated with Fueling Heat Engines

    Directory of Open Access Journals (Sweden)

    Robert C. Hendricks

    2011-01-01

    Full Text Available All hydrocarbon- (HC- fueled heat engine exhaust (tailpipe emissions (<10 to 140 nm contribute as health hazards, including emissions from transportation vehicles (e.g., aircraft and other HC-fueled power systems. CO2 emissions are tracked and, when mapped, show outlines of major transportation routes and cities. Particulate pollution affects living tissue and is found to be detrimental to cardiovascular and respiratory systems where ultrafine particulates directly translocate to promote vascular system diseases potentially detectable as organic vapors. This paper discusses aviation emissions, fueling, and certification issues, including heat engine emissions hazards, detection at low levels and tracking of emissions, and alternate energy sources for general aviation.

  19. Identification and quantification of known polycyclic aromatic hydrocarbons and pesticides in complex mixtures using fluorescence excitation-emission matrices and parallel factor analysis.

    Science.gov (United States)

    Ferretto, Nicolas; Tedetti, Marc; Guigue, Catherine; Mounier, Stéphane; Redon, Roland; Goutx, Madeleine

    2014-07-01

    Polycyclic aromatic hydrocarbons (PAHs) and pesticides are among the most widespread organic contaminants in aquatic environments. Because of their aromatic structure, PAHs and pesticides have intrinsic fluorescence properties in the ultraviolet/blue spectral range. In this study, excitation-emission matrix (EEM) fluorescence spectroscopy and parallel factor (PARAFAC) analysis were used to characterise and discriminate fluorescence signatures of nine PAHs and three pesticides at the μg L(-1) level in the presence of humic substances (0.1-10 mgCL(-1)). These contaminants displayed a diversity of fluorescence signatures regarding spectral position (λEx: 220-335 nm, λEm: 310-414 nm), Stokes shift (39-169 nm) and number of peaks (1-8), with detection limits ranging from 0.02 to 1.29μgL(-1). The EEM/PARAFAC method applied to mixtures of PAHs with humic substances validated a seven-component model that included one humic-like fluorophore and six PAH-like fluorophores. The EEM/PARAFAC method applied to mixtures of pesticides with humic substances validated a six-component model that included one humic-like fluorophore and three pesticide-like fluorophores. The EEM/PARAFAC method adequately quantified most of the contaminants for humic substance concentrations not exceeding 2.5 mg CL(-1). The application of this method to natural (marine) samples was demonstrated through (1) the match between the Ex and Em spectra of PARAFAC components and the Ex and Em spectra of standard PAHs, and (2) the good linear correlations between the fluorescence intensities of PARAFAC components and the PAH concentrations determined by GC-MS.

  20. Polycyclic aromatic hydrocarbons (PAHs) in exhaust emissions from diesel engines powered by rapeseed oil methylester and heated non-esterified rapeseed oil

    Science.gov (United States)

    Vojtisek-Lom, Michal; Czerwinski, Jan; Leníček, Jan; Sekyra, Milan; Topinka, Jan

    2012-12-01

    Polycyclic aromatic hydrocarbons (PAHs) of exhaust emissions were studied in four direct-injection turbocharged four-cylinder diesel engines, with power ratings of 90-136 kW. The engines were operated on biodiesel (B-100), a blend of 30% biodiesel in diesel fuel (B-30), and heated rapeseed oil (RO) in two independent laboratories. Diesel particle filters (DPF) and selective catalytic reduction (SCR) systems were used with B-30 and B-100. Concentrations of individual PAHs sampled in different substrates (quartz, borosilicate fiber and fluorocarbon membrane filters, polyurethane foam) were analyzed using different methods. Benzo[a]pyrene toxic equivalents (BaP TEQ) were calculated using different sets of toxic equivalency factors (TEF). Operation on B-100 without aftertreatment devices, compared to diesel fuel, yielded a mean reduction in PAHs of 73%, consistent across engines and among TEF used. A lower PAH reduction was obtained using B-30. The BaP TEQ reductions on DPF were 91-99% using B-100, for one non-catalyzed DPF, and over 99% in all other cases. The BaP TEQ for heated RO were higher than those for B-100 and one half lower to over twice as high as that of diesel fuel. B-100 and RO samples featured, compared to diesel fuel, a relatively high share of higher molecular weight PAH and a relatively low share of lighter PAHs. Using different sets of TEF or different detection methods did not consistently affect the observed effect of fuels on BaP TEQ. The compilation of multiple tests was helpful for discerning emerging patterns. The collection of milligrams of particulate matter per sample was generally needed for quantification of all individual PAHs.

  1. π-Extended Star-Shaped Polycyclic Aromatic Hydrocarbons based on Fused Truxenes: Synthesis, Self-Assembly, and Facilely Tunable Emission Properties.

    Science.gov (United States)

    Cheng, Cheng; Jiang, Yi; Liu, Cheng-Fang; Zhang, Jian-Dong; Lai, Wen-Yong; Huang, Wei

    2016-12-19

    A new set of star-shaped polycyclic aromatic hydrocarbons (PAHs) based on naphthalene-fused truxenes, TrNaCn (n=1-4), were synthesized and characterized. The synthesis involved a microwave-assisted six-fold Suzuki coupling reaction, followed by oxidative cyclodehydrogenation. Multiple dehydrocyclization products could be effectively isolated in a single reaction, thus suggesting that the oxidative cyclodehydrogenation reaction involved a stepwise ring-closing process. The thermal, optical, and electrochemical properties and the self-assembly behavior of the resulting oxidized samples were investigated to understand the impact of the ring-fusing process on the properties of the star-shaped PAHs. Distinct bathochromic shift of the absorption maxima (λmax ) revealed that the molecular conjugation extended with the stepwise ring-closing reactions. The optical band-gap energy of these PAHs varied significantly on increasing the number of fused rings, thereby resulting in readily tunable emissive properties of the resultant star-shaped PAHs. Interestingly, the generation of rigid "arms" by using perylene analogues caused TrNaC2 and TrNaC3 to show significantly enhanced photoluminescence quantum yields (PLQYs) in solution (η=0.65 and 0.66, respectively) in comparison with those of TrNa and TrNaC1 (η=0.08 and 0.16, respectively). Owing to strong intermolecular interactions, the TrNa precursor was able to self-assemble into rod-like microcrystals, which could be facilely identified by the naked eye, whilst TrNaC1 self-assembled into nanosheets once the naphthalene rings had fused. This study offers a unique platform to gain further insight into-and a better understanding of-the photophysical and self-assembly properties of π-extended star-shaped PAHs.

  2. An Investigation on the Formation of Carbon Nanotubes by Two-Stage Chemical Vapor Deposition

    Directory of Open Access Journals (Sweden)

    M. S. Shamsudin

    2012-01-01

    Full Text Available High density of carbon nanotubes (CNTs has been synthesized from agricultural hydrocarbon: camphor oil using a one-hour synthesis time and a titanium dioxide sol gel catalyst. The pyrolysis temperature is studied in the range of 700–900°C at increments of 50°C. The synthesis process is done using a custom-made two-stage catalytic chemical vapor deposition apparatus. The CNT characteristics are investigated by field emission scanning electron microscopy and micro-Raman spectroscopy. The experimental results showed that structural properties of CNT are highly dependent on pyrolysis temperature changes.

  3. Vapor Bubbles

    Science.gov (United States)

    Prosperetti, Andrea

    2017-01-01

    This article reviews the fundamental physics of vapor bubbles in liquids. Work on bubble growth and condensation for stationary and translating bubbles is summarized and the differences with bubbles containing a permanent gas stressed. In particular, it is shown that the natural frequency of a vapor bubble is proportional not to the inverse radius, as for a gas bubble, but to the inverse radius raised to the power 2/3. Permanent gas dissolved in the liquid diffuses into the bubble with strong effects on its dynamics. The effects of the diffusion of heat and mass on the propagation of pressure waves in a vaporous bubbly liquid are discussed. Other topics briefly touched on include thermocapillary flow, plasmonic nanobubbles, and vapor bubbles in an immiscible liquid.

  4. The discovery of a new infrared emission feature at 1905 wavenumbers (5.25 microns) in the spectrum of BD + 30 deg 3639 and its relation to the polycyclic aromatic hydrocarbon model

    Science.gov (United States)

    Allamandola, L. J.; Bregman, J. D.; Sandford, S. A.; Tielens, A. G. G. M.; Witteborn, F. C.

    1989-01-01

    A new IR emission feature at 1905/cm (5.25 microns) has been discovered in the spectrum of BD + 30 deg 3639. This feature joins the family of well-known IR emission features at 3040, 2940, 1750, 1610, '1310', 1160, and 890/cm. The origin of this new feature is discussed and it is assigned to an overtone or combination band involving C-H bending modes of polycyclic aromatic hydrocarbons (PAHs). Laboratory work suggests that spectral studies of the 2000-1650/cm region may be very useful in elucidating the molecular structure of interstellar PAHs. The new feature, in conjunction with other recently discovered spectral structures, suggests that the narrow IR emission features originate in PAH molecules rather than large carbon grains.

  5. BACT Fugitive Emissions of Hydrocarbons

    Science.gov (United States)

    This document may be of assistance in applying the New Source Review (NSR) air permitting regulations including the Prevention of Significant Deterioration (PSD) requirements. This document is part of the NSR Policy and Guidance Database. Some documents in the database are a scanned or retyped version of a paper photocopy of the original. Although we have taken considerable effort to quality assure the documents, some may contain typographical errors. Contact the office that issued the document if you need a copy of the original.

  6. Experimental Study on Emissions of Polycyclic Aromatic Hydrocarbons of Unleaded Gasoline%汽油多环芳香烃排放的试验研究

    Institute of Scientific and Technical Information of China (English)

    李西秦; 蔡仁华; 曹淼龙; 刘冰

    2011-01-01

    In order to study the effect of three-way catalytic converter on generation of polycyclic aromatic hydrocarbons (PAH)in gasoline combustion process, tests were made in a HL495IQ electronic fuel injection gasoline engine. The emissions of several kinds of PAHs are measured by a gas chromatography - mass spectrometry (GC-MS) analyzer. The test results show that PAH is generated mainly by fuel which is not burnt completely at exhaust temperature of 200~600 t. With the increase of exhaust temperature to 600-800℃, the fuel will be broken up into more free radicals, which results in more PAH being generated. In three-way catalytic converter, PAH may be synthesized or converted, the nature and reaction condition of PAH determines which trend dominates.%为了解三元催化器对汽油燃烧过程中多环芳香烃生成的影响,在HL495IQ电喷汽油机上进行了台架试验,通过气相色谱一质谱联用(GC-MS)分析仪测试了几种多环芳香烃的排放量.试验结果表明,排气温度在200~600℃时,多环芳香烃主要源于未完全燃烧的燃油;排气温度在600~800℃时,随温度的升高燃油裂解出更多的自由基团,从而促使生成更多的多环芳香烃.在三元催化器中存在着多环芳香烃的合成与转化2个趋势,哪个趋势占主导地位取决于多环芳香烃各白的性质和反应条件.

  7. Optrode for sensing hydrocarbons

    Science.gov (United States)

    Miller, Holly; Milanovich, Fred P.; Hirschfeld, Tomas B.; Miller, Fred S.

    1987-01-01

    A two-phase system employing the Fujiwara reaction is provided for the fluorometric detection of halogenated hydrocarbons. A fiber optic is utilized to illuminate a column of pyridine trapped in a capillary tube coaxially attached at one end to the illuminating end of the fiber optic. A strongly alkaline condition necessary for the reaction is maintained by providing a reservoir of alkali in contact with the column of pyridine, the surface of contact being adjacent to the illuminating end of the fiber optic. A semipermeable membrane caps the other end of the capillary tube, the membrane being preferentially permeable to the halogenated hydrocarbon and but preferentially impermeable to water and pyridine. As the halogenated hydrocarbon diffuses through the membrane and into the column of pyridine, fluorescent reaction products are formed. Light propagated by the fiber optic from a light source, excites the fluorescent products. Light from the fluorescence emission is also collected by the same fiber optic and transmitted to a detector. The intensity of the fluorescence gives a measure of the concentration of the halogenated hydrocarbons.

  8. Characterization of hydrocarbon utilizing fungi from hydrocarbon ...

    African Journals Online (AJOL)

    Prof. Ogunji

    hydrocarbon polluted sediments and water .... ecosystem may result in selective increase or decrease in microbial population (Okpokwasili ... been implicated in degradation of hydrocarbons such as crude oil, polyaromatic hydrocarbons and.

  9. Using Conventional Monitoring Wells to Collect Data Necessary to Understand Petroleum Vapor Intrusion (PVI)

    Science.gov (United States)

    Recent work has clearly established that the possibility for vapor intrusion of petroleum hydrocarbons is greatly reduced by aerobic biodegradation of the hydrocarbons in unsaturated soil. The rate and extent of aerobic biodegradation of benzene (or any other fuel hydrocarbon) in...

  10. Using Conventional Monitoring Wells to Collect Data Necessary to Understand Petroleum Vapor Intrusion (PVI)

    Science.gov (United States)

    Recent work has clearly established that the possibility for vapor intrusion of petroleum hydrocarbons is greatly reduced by aerobic biodegradation of the hydrocarbons in unsaturated soil. The rate and extent of aerobic biodegradation of benzene (or any other fuel hydrocarbon) in...

  11. Federal Air Pollutant Emission Regulations and Preliminary Estimates of Potential-to-Emit from Biorefineries. Pathway #1: Dilute-Acid and Enzymatic Deconstruction of Biomass-to-Sugars and Biological Conversion of Sugars-to-Hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yimin [National Renewable Energy Lab. (NREL), Golden, CO (United States); Bhatt, Arpit [National Renewable Energy Lab. (NREL), Golden, CO (United States); Heath, Garvin [National Renewable Energy Lab. (NREL), Golden, CO (United States); Thomas, Mae [Eastern Research Group, Lexington, MA (United States); Renzaglia, Jason [Eastern Research Group, Lexington, MA (United States)

    2016-02-01

    Biorefineries are subject to environmental laws, including complex air quality regulations that aim to protect and improve the quality of the air. These regulations govern the amount of certain types of air pollutants that can be emitted from different types of emission sources. To determine which federal air emission regulations potentially apply to the sugars-to-hydrocarbon (HC) biorefinery, we first identified the types of regulated air pollutants emitted to the ambient environment by the biorefinery or from specific equipment. Once the regulated air pollutants are identified, we review the applicability criteria of each federal air regulation to determine whether the sugars-to-HC biorefinery or specific equipment is subject to it. We then estimate the potential-to-emit of pollutants likely to be emitted from the sugars-to-HC biorefinery to understand the air permitting requirements.

  12. Structure-reactivity correlation of diesel soot and characterization of polycyclic aromatic hydrocarbons and carbonyls in biofuel emissions; Struktur-Reaktivitaets-Korrelation von Dieselruss und Charakterisierung von PAHs und Carbonylen im Abgas von Biokraftstoffen

    Energy Technology Data Exchange (ETDEWEB)

    Knauer, Markus

    2009-12-29

    This work reports on the determination of the structure-reactivity correlation of soot using Raman microscopy (RM) and temperature programmed oxidation (TPO), as well as on changes in the emission level of polycyclic aromatic hydrocarbons (PAH) and carbonyls at the combustion of biofuels. To characterize the reactivity of soot the combustion behaviour of model- and diesel soot has been determined by means of TPO in the presence of oxygen. In this context, spark-discharge soot and graphite powder were applied as model substances, and EURO VI and IV diesel soot as real-diesel soots. The structure of soot samples was investigated by RM and structural changes during the TPO were observed. In order to make a statement about the changes in PAH and carbonyl compound emissions during combustion of biofuels, samples were taken at different engine testbenches. Fossil fuel, biodiesel and vegetable oil were used during this study, as well as fuel mixtures with different biofuel fractions.

  13. The Infrared Spectra of Polycyclic Aromatic Hydrocarbons with Excess Peripheral H Atoms (H(sub n)-PAHs) and their Relation to the 3.4 and 6.9 Micrometer PAH Emission Features

    Science.gov (United States)

    Sandford, Scott A.; Bernstein, Max P.; Materese, Christopher K.

    2013-01-01

    A population of polycyclic aromatic hydrocarbons (PAHs) and related materials are thought to be responsible for the family of infrared emission features that are seen towards a wide variety of astrophysical environments. A potentially important subclass of these materials are polycyclic aromatic hydrocarbons whose edges contain excess H atoms (H(sub n)-PAHs). While it has been suggested that this type of compound may be present in the interstellar population, it has been difficult to properly assess this possibility because of a lack of suitable infrared laboratory spectra to assist with analysis of the astronomical data. We present the 4000-500 cm(exp -1) (2.5-20 micrometers) infrared spectra of 23 H(sub n)-PAHs and related molecules isolated in argon matrices, under conditions suitable for use in the interpretation of astronomical data. The spectra of molecules with mixed aromatic and aliphatic domains show unique characteristics that distinguish them from their fully aromatic PAH equivalents. We discuss the changes to the spectra of these types of molecules as they transition from fully aromatic to fully aliphatic forms. The implications for the interpretation of astronomical spectra are discussed with specific emphasis on the 3.4 and 6.9 micrometer features. Laboratory data is compared with emission spectra from IRAS 21282+5050, an object with normal PAH emission features, in addition to IRAS 22272+5435 and IRAS 0496+3429, two protoplanetary nebulae with abnormally large 3.4 micrometer features. We show that 'normal' PAH emission objects contain relatively few H(sub n)-PAHs in their emitter populations, but less evolved protoplanetary nebulae may contain significant abundances of these molecules.

  14. Reduction of Particulate Emissions in Turbine Engines Using the +100 Additive

    Science.gov (United States)

    2006-06-01

    element oscillating microbalance THC total unburned hydrocarbon UDRI University of Dayton Research Institute UHC unburned hydrocarbons UMR...all tests Primary Reduced gaseous pollutant emissions 20% reduction in CO, NOx and unburned hydrocarbons ( UHC ) emissions for all test conditions

  15. Etude d'équations d'état en vue de représenter les propriétés PVT et les équilibres liquide-vapeur d'hydrocarbures Equations of State for Representing Pvt Properties and Vapor-Liquid Equilibria of Hydrocarbons

    Directory of Open Access Journals (Sweden)

    Neau E.

    2006-11-01

    Full Text Available Une étude comparative de plusieurs équations d'état issues de la théorie de van der Waals a été effectuée dans le but de sélectionner des modèles capables de calculer les propriétés PVT d'hydrocarbures dans un large domaine de pression et température. 34 hydrocarbures de différentes tailles et structures ont été sélectionnés. Les données expérimentales d'équilibres liquide-vapeur (pressions de vapeur, volumes des liquides et les propriétés PVT de fluides comprimés ont été systématiquement comparées avec des résultats obtenus au moyen de différentes équations d'état. Il est apparu que seules les équations d'état complexes (notamment l'équation COR sont en mesure de représenter correctement les propriétés volumétriques dans un large domaine de température et de pression, le voisinage du point critique inclu. A comparative study of several equations of state (EOS derived from the van der Waals theory was performed. The aim was to select the models able to represent PVT properties of hydrocarbons in large pressure and temperature ranges. 34 hydrocarbons of various sizes and structures were selected. Experimental data of vapor liquid equilibria (vapor pressures and liquid volumes and PVT properties of compressed fluids were systematically compared with results obtained using selected EOS. It was shown that only the complex EOS (especially the COR equation are able to represent volumetric properties in wide temperature and presssure ranges, the critical region included.

  16. Apparatus for hydrocarbon extraction

    Science.gov (United States)

    Bohnert, George W.; Verhulst, Galen G.

    2013-03-19

    Systems and methods for hydrocarbon extraction from hydrocarbon-containing material. Such systems and methods relate to extracting hydrocarbon from hydrocarbon-containing material employing a non-aqueous extractant. Additionally, such systems and methods relate to recovering and reusing non-aqueous extractant employed for extracting hydrocarbon from hydrocarbon-containing material.

  17. Emission characteristics of pulse-periodic barrier-discharge plasma in a mixture of krypton with argon and liquid freon vapor

    Science.gov (United States)

    Shuaibov, A. K.; Minya, A. I.; Gritsak, R. V.; Gomoki, Z. T.

    2014-02-01

    Radiation of a nanosecond barrier discharge in a mixture of krypton, argon, and carbon-tetrachloride vapor is studied in the spectral range of 150-300 nm. The plasma radiation spectra and the dependences of the intensities of the 258 nm Cl2( D' → A'), 222 nm KrCl( B → X), and 175 nm ArCl( B → X) bands on the partial pressure of liquid freon vapor, argon, and krypton, as well as on the discharge excitation conditions, are studied. The optimal compositions of gas mixtures for creating a broadband UV-VUV emitter based on the band system of argon chloride, krypton chloride, and chlorine molecule are determined.

  18. Wall quench and flammability limit effects on exhaust hydrocarbon emissions. Final technical report, Phase 5: 1 August 1980-30 September 1980

    Energy Technology Data Exchange (ETDEWEB)

    Fendell, F.

    1980-10-01

    Progress is reported in a project concerned with simple modeling and laboratory experiments to elucidate the mechanisms whereby trace amounts of unburned hydrocarbons may persist after the combustion event in Otto-cycle-type internal-combustion-engine cylinders, and the fate of these residual hydrocarbons during the power-stroke and exhaust-event portions of the cycle. The motivation for the research is that a highly fuel-lean fast-burn design for the spark-ignition homogeneous-charge, four-stroke engine may permit exceptionally fuel-efficient operation of this highly driveable, relatively well-understood automotive engine. Work during this period concentrated on the mathematical modelling of wall quenching and turbulent flame propagation. (LCL)

  19. Relative contribution of oxygenated hydrocarbons to the total biogenic VOC emissions of selected mid-European agricultural and natural plant species

    Science.gov (United States)

    König, Georg; Brunda, Monika; Puxbaum, Hans; Hewitt, C. Nicholas; Duckham, S. Craig; Rudolph, Jochen

    Emission rates of more than 50 individual VOCs were determined for eight plant species and three different types of grass land typical for natural deciduous and agricultural vegetation in Austria. In addition to the emissions of isoprene and monoterpenes, 33 biogenic oxygenated volatile organic compounds (BOVOCs) were detected. Of these, 2-methyl-l-propanol, 1-butanal, 2-butanal, 1-pentanol, 3-pentanol, 1-hexanol, 6-methyl-5-hepten-2-one, butanal and ethylhexylacetate were observed for the first time as plant emissions. In terms of prevalence of one of the groups of emitted VOCs (isoprene, terpenes, BOVOCs) the grain plants wheat and rye, grape, oilseed rape and the decidous trees hombeam and birch could be classified as "BOVOC"-emitters. For the grass plots examined, BOVOCs and terpenes appear to be of equal importance. The emission rates of the total assigned organic plant emissions ranged from 0.01 μ g -1 h -1 for wheat to 0.8 μg g -1 h -1 for oak (based on dry leaf weight). Intercomparison with available data from other studies show that our emission rates are rather at the lower end of reported ranges. The influence of the stage of growth was examined for rye, rape (comparing emissions of blossoming and nonblossoming plants) and for grape (with and without fruit). Emission rate differences for different stages of growth varied from nondetectable for blossoming and nonblossoming rye to a factor of six for the grape with fruits vs grape without fruits (emission rate based on dry leaf weight). The major decidous tree in Austria (beech) is a terpene emitter, with the contribution of BOVOCs below 5% of the total assigned emissions of 0.2 μg g -1 h -1 for the investigations of 20°C.

  20. The discovery of a new infrared emission feature at 1905 wavenumbers (5.25 microns) in the spectrum of BD +30 degrees 3639 and its relation to the polycyclic aromatic hydrocarbon model

    Science.gov (United States)

    Allamandola, L. J.; Bregman, J. D.; Sandford, S. A.; Tielens, A. G.; Witteborn, F. C.; Wooden, D. H.; Rank, D.

    1989-01-01

    We have discovered a new IR emission feature at 1905 cm-1 (5.25 microns) in the spectrum of BD +30 degrees 3639. This feature joins the family of well-known IR emission features at 3040, 2940, 1750, 1610, "1310," 1160, and 890 cm-1 (3.3, 3.4, 5.7, 6.2, "7.7," 8.6, and 11.2 microns). The origin of this new feature is discussed and it is assigned to an overtone or combination band involving C-H bending modes of polycyclic aromatic hydrocarbons (PAHs). Laboratory work suggests that spectral studies of the 2000-1650 cm-1 (5.0-6.1 microns) region may be very useful in elucidating the molecular structure of interstellar PAHs. The new feature, in conjunction with other recently discovered spectral structure, suggests that the narrow IR emission features originate in PAH molecules rather than large carbon grains. Larger species are likely to be the source of the broad underlying "plateaus" seen in many of the spectra.

  1. Measurements of emission rates of hydrocarbons from sunflower as a function of temperature, light intensity and stress (ozone levels); Bestimmung von Emissionsraten pflanzlicher Kohlenwasserstoffe bei Sonnenblumen in Abhaengigkeit von Temperatur, Lichtintensitaet und Stress, insbesondere von der Belastung mit Ozon

    Energy Technology Data Exchange (ETDEWEB)

    Schuh, G.; Wildt, J.; Kley, D.

    1996-08-01

    The emission rates of isoprene, mono- and sesquiterpenes from sunflower (Helianthus annuus L. cv. giganteus) were determined in an environmental chamber, a continuously stirred tank reactor. {alpha}-pinene, {beta}-caryophyllene and two oxygenated compounds were emitted. The emission rates of all terpenes increased exponentially with temperature. Substance specific differences of the rate of increase of the emission rates were observed. For all substances the dependence of their emission rates on temperature increased with increasing light intensity. Increasing lightflux resulted in an increase of the emission rates for all substances. The raise of emission rates with lightflux was dependent on temperature and increased with increasing temperature. During periods without plant stress the emission rates exhibited a good correlation with the rate of transpiration as well as with the rate of net photosynthesis. Sunflowers emitted higher amounts of terpenes when they were stressed by mechanical, wounding and ozone treatment as well as nutrient- or water deficiency. The emission rates increased by a factor of 5-300. Exposure with ozone had an effect on hydrocarbon emission rates with a delay-time. 3-4 h after exposure with 25-120 ppb ozone the emission rates increased by factor of 5-100. This increase was only observed on the first day of exposure. Nutrient deficiency resulted in an increase of emission rates by a factor of 10-300. In situations of mechanical, wounding and ozone stress, substance specific changes in the emission spectrum were observed. A model was developed to explain the observed phenomena. The main pathway of ozone loss in the chamber is caused by the uptake through the stomata of the plants. However, up to 50% of the ozone loss must be explained by other processes indirectly caused by the plants. (orig./MG) [Deutsch] In Laborversuchen wurden Emissionsraten biogener Kohlenwasserstoffe von Sonnenblumen gemessen. Die groessten Emissionsraten wiesen die

  2. Removal of hydrogen sulfide as ammonium sulfate from hydropyrolysis product vapors

    Energy Technology Data Exchange (ETDEWEB)

    Marker, Terry L.; Felix, Larry G.; Linck, Martin B.; Roberts, Michael J.

    2017-03-14

    A system and method for processing biomass into hydrocarbon fuels that includes processing a biomass in a hydropyrolysis reactor resulting in hydrocarbon fuels and a process vapor stream and cooling the process vapor stream to a condensation temperature resulting in an aqueous stream. The aqueous stream is sent to a catalytic reactor where it is oxidized to obtain a product stream containing ammonia and ammonium sulfate. A resulting cooled product vapor stream includes non-condensable process vapors comprising H.sub.2, CH.sub.4, CO, CO.sub.2, ammonia and hydrogen sulfide.

  3. THE INFRARED SPECTRA OF POLYCYCLIC AROMATIC HYDROCARBONS WITH EXCESS PERIPHERAL H ATOMS (H {sub n} -PAHs) AND THEIR RELATION TO THE 3.4 AND 6.9 {mu}m PAH EMISSION FEATURES

    Energy Technology Data Exchange (ETDEWEB)

    Sandford, Scott A.; Bernstein, Max P. [NASA-Ames Research Center, Mail Stop 245-6, Moffett Field, CA 94035-1000 (United States); Materese, Christopher K., E-mail: Scott.A.Sandford@nasa.gov [SETI Institute, 189 Bernardo Avenue, Suite 100, Mountain View, CA 94043 (United States)

    2013-03-01

    Polycyclic aromatic hydrocarbons (PAHs) are likely responsible for the family of infrared emission features seen in a wide variety of astrophysical environments. A potentially important subclass of these materials are PAHs whose edges contain excess H atoms (H {sub n} -PAHs). This type of compound may be present in space, but it has been difficult to assess this possibility because of a lack of suitable laboratory spectra to assist with analysis of astronomical data. We present 4000-500 cm{sup -1} (2.5-20 {mu}m) infrared spectra of 23 H {sub n} -PAHs and related molecules isolated in argon matrices under conditions suitable for interpretation of astronomical data. Spectra of molecules with mixed aromatic and aliphatic domains show characteristics that distinguish them from fully aromatic PAH equivalents. Two major changes occur as PAHs become more hydrogenated: (1) aromatic C-H stretching bands near 3.3 {mu}m weaken and are replaced with stronger aliphatic bands near 3.4 {mu}m, and (2) aromatic C-H out-of-plane bending mode bands in the 11-15 {mu}m region shift and weaken concurrent with growth of a strong aliphatic -CH{sub 2}- deformation mode near 6.9 {mu}m. Implications for interpreting astronomical spectra are discussed with emphasis on the 3.4 and 6.9 {mu}m features. Laboratory data is compared with emission spectra from IRAS 21282+5050, an object with normal PAH emission features, and IRAS 22272+5435 and IRAS 0496+3429, two protoplanetary nebulae with abnormally large 3.4 {mu}m features. We show that 'normal' PAH emission objects contain relatively few H {sub n} -PAHs in their emitter populations, but less evolved protoplanetary nebulae may contain significant abundances of these molecules.

  4. The hydrocarbon sphere

    Energy Technology Data Exchange (ETDEWEB)

    Mandev, P.

    1984-01-01

    The hydrocarbon sphere is understood to be the area in which hydrocarbon compounds are available. It is believed that the lower boundary on the hydrocarbon sphere is most probably located at a depth where the predominant temperatures aid in the destruction of hydrocarbons (300 to 400 degrees centigrade). The upper limit on the hydrocarbon sphere obviously occurs at the earth's surface, where hydrocarbons oxidize to H20 and CO2. Within these ranges, the occurrence of the hydrocarbon sphere may vary from the first few hundred meters to 15 kilometers or more. The hydrocarbon sphere is divided into the external (mantle) sphere in which the primary gas, oil and solid hydrocarbon fields are located, and the internal (metamorphic) sphere containing primarily noncommercial accumulations of hydrocarbon gases and solid carbon containing compounds (anthraxilite, shungite, graphite, etc.) based on the nature and scale of hydrocarbon compound concentrations (natural gas, oil, maltha, asphalt, asphaltite, etc.).

  5. Comparison of Practical Investigations for CO Emissions Emitted From Single Cylinder S. I. Engine Fueled With Different Kinds of Hydrocarbon Fuels and Hydrogen

    Directory of Open Access Journals (Sweden)

    Khalil Ibrahim Abaas

    2011-01-01

    Full Text Available Liquefied petroleum gas (LPG, Natural gas (NG and hydrogen were all used to operate spark ignition internal combustion engine Ricardo E6. A comparison of CO emissions emitted from each case, with emissions emitted from engine fueled with gasoline as a fuel is conducted.The study was accomplished when engine operated at HUCR for gasoline n(8:1, was compared with its operation at HUCR for each fuel. Compression ratio, equivalence ratio and spark timing were studied at constant speed 1500 rpm.CO concentrations were little at lean ratios; it appeared to be effected a little with equivalence ratio in this side, at rich side its values became higher, and it appeared to be effected by equivalence ratio highly, the results showed that CO emissions resulted from gasoline engine were higher than that resulted from using LPG and NG all the time; while hydrogen engine emitted extremely low CO concentrations.

  6. Emissions of non-methane organic compounds from a grassland site

    Energy Technology Data Exchange (ETDEWEB)

    Fukui, Yoshiko; Doskey, P.V.

    1996-03-01

    A mixture of oxygenated hydrocarbons (OxHCs), isoprene, and monoterpenes was detected in the emissions from a grassland site in the Midwestern United States. A plot dominated by crown vetch (Coronilla varia) and bluegrass (Poa spp.), exhibited a constant decrease in emissions of total non-methane organic compounds (NMOCs) from 580 {mu}g m{sup -2} hr{sup -1} in June 1992 to 150 {mu}g m{sup - 2} hr{sup -1} in October 1992, except for a slight increase in August. Oxygenated hydrocarbons (methanol, acetaldehyde, and acetone) and terpenes (isoprene, limonene, myrcene, {alpha}-pinene, and {beta}- pinene) composed about 90% and 10% of the identified NMOC emissions, respectively. Isoprene represented about 10% of the terpene emissions. Total NMOC emission rates based on vegetative biomass averaged 2.3 {mu}g g{sup -1} hr{sup -1}, with 10% of the identified NMOCs attributed to monoterpenes and the remainder mainly OxHCs. Over the course of the investigation, the relationship between the monoterpene emission rate and the temperature for a single plot was logarithmic and similar to the one between compound vapor pressure and temperature. However, emission rates normalized to temperature decreased throughout the summer and fall, indicating that parameterizations of emission rates from herbaceous plants must include a factor to compensate for environmental conditions such as soil moisture and nutrient deposition, which affect plant phenology and the seasonal pattern of species dominance.

  7. Control and reduction of NOx emissions on light hydrocarbons combustion in fluidized bed combustors: a technological prospection surveys; Controle e reducao de emissoes de NOx durante queima de hidrocarbonetos leves em combustores a leito fluidizado: um estudo de prospeccao tecnologica

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Douglas Alves; Winter, Eduardo [Instituto Nacional da Propriedade Industrial (INPI), Rio de Janeiro, RJ (Brazil)

    2008-07-01

    The present paper aims a technological prospecting study of the main technological agents involved in industrial light hydrocarbons combustion process. More specifically, the work approaches technologies applied to nitrogen oxides emissions control and reduction. Nitrogen oxides are typically known as 'NOx' (NO, N{sub 2}O, NO{sub 2}). 'NOx' are byproducts from fuel burning in combustion systems, including also in fluidized bed combustion systems. The technological prospecting study employed 'technology foresight' as tool for evaluating the technological perspectives of the thermal generation, basis on environment protection. Such technological perspectives of the thermal generation were evaluated through invention patent documents. The query methodology for obtaining of patent documents employed a free patent base, known as ESPACENET. Additionally, the documents obtained were evaluated, considering beyond the countries and the publication dates, technological perspectives employed to 'NOx' emissions control and reduction. It is very important to highlight around 70% of the industrial technological information are just found in invention patent documents. (author)

  8. Iron bromide vapor laser

    Science.gov (United States)

    Sukhanov, V. B.; Shiyanov, D. V.; Trigub, M. V.; Dimaki, V. A.; Evtushenko, G. S.

    2016-03-01

    We have studied the characteristics of a pulsed gas-discharge laser on iron bromide vapor generating radiation with a wavelength of 452.9 nm at a pulse repetition frequency (PRF) of 5-30 kHz. The maximum output power amounted to 10 mW at a PRF within 5-15 kHz for a voltage of 20-25 kV applied to electrodes of the discharge tube. Addition of HBr to the medium produced leveling of the radial profile of emission. Initial weak lasing at a wavelength of 868.9 nm was observed for the first time, which ceased with buildup of the main 452.9-nm line.

  9. Hydrogenated Polycyclic Aromatic Hydrocarbons and the 2940 and 2850 Wavenumber (3.40 and 3.51 micron) Infrared Emission Features

    Science.gov (United States)

    Bernstein, Max P.; Sandford, Scott A.; Allamadola, Louis J.

    1996-01-01

    The 3150-2700/cm (3.17-3.70 micron) range of the spectra of a number of Ar-matrix-isolated PAHs containing excess H atoms (H(sub n)-PAHS) are presented. This region covers features produced by aromatic and aliphatic C-H stretching vibrations as well as overtone and combination bands involving lower lying fundamentals. The aliphatic C-H stretches in molecules of this type having low to modest excess H coverage provide excellent fits to a number of the weak emission features superposed on the plateau between 3080 and 2700/cm (3.25 and 3.7 micron) in the spectra of many planetary nebulae, reflection nebulae, and H II regions. Higher H coverage is implied for a few objects. We compare these results in context with the other suggested identifications of the emission features in the 2950-2700/cm (3.39-3.70 micron) region and briefly discuss their astrophysical implications.

  10. HANFORD CHEMICAL VAPORS WORKER CONCERNS & EXPOSURE EVALUATION

    Energy Technology Data Exchange (ETDEWEB)

    ANDERSON, T.J.

    2006-12-20

    Chemical vapor emissions from underground hazardous waste storage tanks on the Hanford site in eastern Washington State are a potential concern because workers enter the tank farms on a regular basis for waste retrievals, equipment maintenance, and surveillance. Tank farm contractors are in the process of retrieving all remaining waste from aging single-shell tanks, some of which date to World War II, and transferring it to newer double-shell tanks. During the waste retrieval process, tank farm workers are potentially exposed to fugitive chemical vapors that can escape from tank headspaces and other emission points. The tanks are known to hold more than 1,500 different species of chemicals, in addition to radionuclides. Exposure assessments have fully characterized the hazards from chemical vapors in half of the tank farms. Extensive sampling and analysis has been done to characterize the chemical properties of hazardous waste and to evaluate potential health hazards of vapors at the ground surface, where workers perform maintenance and waste transfer activities. Worker concerns. risk communication, and exposure assessment are discussed, including evaluation of the potential hazards of complex mixtures of chemical vapors. Concentrations of vapors above occupational exposure limits-(OEL) were detected only at exhaust stacks and passive breather filter outlets. Beyond five feet from the sources, vapors disperse rapidly. No vapors have been measured above 50% of their OELs more than five feet from the source. Vapor controls are focused on limited hazard zones around sources. Further evaluations of vapors include analysis of routes of exposure and thorough analysis of nuisance odors.

  11. Raman characteristics of hydrocarbon and hydrocarbon inclusions

    Institute of Scientific and Technical Information of China (English)

    ZHANG Nai; TIAN ZuoJi; LENG YingYing; WANG HuiTong; SONG FuQing; MENG JianHua

    2007-01-01

    The Raman spectrograms of hydrocarbon standard samples show that: (1) the Raman spectrogram of normal paraffin has very strong peaks of methyl and methylene (from 2700 cm-1 to 2970 cm-1); (2)branch methyl has the particular peak of 748 cm-1±; (3) six cyclic has the particular peak of 804 cm-1±; (4)phenyl has two particular peaks of 988 cm-1± and 3058 cm-1± and the 988 cm-1± peak is stronger than the 3058 cm-1± peak; and (5) hexene has three alkenyl spectrum peaks of 1294 cm-1±, 1635 cm-1± and 2996 cm-1±, with the 1635 cm-1± peak being the strongest, showing that the number of carbon in hydrocarbon does not affect its Raman spectrogram, and the hydrocarbon molecular structure and base groups affect its Raman spectrogram, the same hydrocarbons (such as normal paraffin) have the same Raman spectrogram; the types (such as CH4, C2H6, C3H8) and the content of hydrocarbon in oil inclusions are not estimated by their characteristic Raman peaks. According to the Raman spectrograms of hydrocarbon compositions, the Raman spectrogram of hydrocarbon inclusion can be divided into five types: saturated hydrocarbon Raman spectrogram, fluoresce Raman spectrogram, saturated hydrocarbon bitumen Raman spectrogram, bitumen Raman spectrogram, and ethane Raman spectrogram.And according to the characteristics of Raman spectrogram, hydrocarbon inclusions can be divided into five types: saturated hydrocarbon inclusion, less saturated hydrocarbon (oil or gas) inclusion,saturated hydrocarbon bitumen inclusion, bitumen inclusion, and methane water inclusion.

  12. Raman characteristics of hydrocarbon and hydrocarbon inclusions

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The Raman spectrograms of hydrocarbon standard samples show that: (1) the Raman spectrogram of normal paraffin has very strong peaks of methyl and methylene (from 2700 cm-1 to 2970 cm-1); (2) branch methyl has the particular peak of 748 cm-1±; (3) six cyclic has the particular peak of 804 cm-1±; (4) phenyl has two particular peaks of 988 cm-1± and 3058 cm-1± and the 988 cm-1± peak is stronger than the 3058 cm-1± peak; and (5) hexene has three alkenyl spectrum peaks of 1294 cm-1±, 1635 cm-1± and 2996 cm-1±, with the 1635 cm-1± peak being the strongest, showing that the number of carbon in hy-drocarbon does not affect its Raman spectrogram, and the hydrocarbon molecular structure and base groups affect its Raman spectrogram, the same hydrocarbons (such as normal paraffin) have the same Raman spectrogram; the types (such as CH4, C2H6, C3H8) and the content of hydrocarbon in oil inclu-sions are not estimated by their characteristic Raman peaks. According to the Raman spectrograms of hydrocarbon compositions, the Raman spectrogram of hydrocarbon inclusion can be divided into five types: saturated hydrocarbon Raman spectrogram, fluoresce Raman spectrogram, saturated hydro-carbon bitumen Raman spectrogram, bitumen Raman spectrogram, and ethane Raman spectrogram. And according to the characteristics of Raman spectrogram, hydrocarbon inclusions can be divided into five types: saturated hydrocarbon inclusion, less saturated hydrocarbon (oil or gas) inclusion, saturated hydrocarbon bitumen inclusion, bitumen inclusion, and methane water inclusion.

  13. Chemical Analysis of Hydrocarbon Grease from Spin Bearing Tests

    Science.gov (United States)

    1982-09-30

    antioxidant but rather to some grease degradation products. (The antioxidant is expected to vaporize and leave the grease under vacuum.) The gas...to 10-3 torr level, phenyl-8- naphthylamIne Is sufficiently volatile to vaporize and leave the grease. The appearance of the solitary, hydrocarbon...Configuration of 2,4- Decadienals Isolated from Oils Containing Linoleic Acid," Nature 185, 310-311 (1960). 7. B. G. Tarladgis, and B. M. Watts

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

    Institute of Scientific and Technical Information of China (English)

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

    2013-01-01

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

  15. Water vapor release from biofuel combustion

    Directory of Open Access Journals (Sweden)

    R. S. Parmar

    2008-03-01

    Full Text Available We report on the emission of water vapor from biofuel combustion. Concurrent measurements of carbon monoxide and carbon dioxide are used to scale the concentrations of water vapor found, and are compared to carbon in the biofuel. Fuel types included hardwood (oak and African musasa, softwood (pine and spruce, partly with green needles, and African savanna grass. The session-averaged ratio of H2O to the sum of CO and CO2 in the emissions from 16 combustion experiments ranged from 1.2 to 3.7 on average, indicating the presence of water that is not chemically bound. This biofuel moisture content ranged from 33% in the dry African hardwood, musasa, to 220% in fresh pine branches with needles. The moisture content from fresh biofuel contributes distinctly to the water vapor in biomass burning emissions, and its influence on meteorology needs to be evaluated.

  16. Water vapor release from biofuel combustion

    Science.gov (United States)

    Parmar, R. S.; Welling, M.; Andreae, M. O.; Helas, G.

    2008-03-01

    We report on the emission of water vapor from biofuel combustion. Concurrent measurements of carbon monoxide and carbon dioxide are used to scale the concentrations of water vapor found, and are compared to carbon in the biofuel. Fuel types included hardwood (oak and African musasa), softwood (pine and spruce, partly with green needles), and African savanna grass. The session-averaged ratio of H2O to the sum of CO and CO2 in the emissions from 16 combustion experiments ranged from 1.2 to 3.7 on average, indicating the presence of water that is not chemically bound. This biofuel moisture content ranged from 33% in the dry African hardwood, musasa, to 220% in fresh pine branches with needles. The moisture content from fresh biofuel contributes distinctly to the water vapor in biomass burning emissions, and its influence on meteorology needs to be evaluated.

  17. Water vapor release from biomass combustion

    Science.gov (United States)

    Parmar, R. S.; Welling, M.; Andreae, M. O.; Helas, G.

    2008-10-01

    We report on the emission of water vapor from biomass combustion. Concurrent measurements of carbon monoxide and carbon dioxide are used to scale the concentrations of water vapor found, and are referenced to carbon in the biomass. The investigated fuel types include hardwood (oak and African musasa), softwood (pine and spruce, partly with green needles), and African savanna grass. The session-averaged ratio of H2O to the sum of CO and CO2 in the emissions from 16 combustion experiments ranged from 1.2 to 3.7, indicating the presence of water that is not chemically bound. This non-bound biomass moisture content ranged from 33% in the dry African hardwood, musasa, to 220% in fresh pine branches with needles. The moisture content from fresh biomass contributes significantly to the water vapor in biomass burning emissions, and its influence on the behavior of fire plumes and pyro-cumulus clouds needs to be evaluated.

  18. 太原市多环芳烃(PAHs)排放清单与分布特征分析%Estimation of annual emission and distribution characteristics of polycyclic aromatic hydrocarbons (PAHs) in Taiyuan

    Institute of Scientific and Technical Information of China (English)

    蒋秋静; 李跃宇; 胡新新; 卢彬; 陶澍; 王戎

    2013-01-01

    根据太原市11种主要排放源的排放因子和活动量数据,估算了美国国家环境保护局(US EPA)优先控制污染物清单中16种多环芳烃(PAHs)的年排放量.结果表明2010年太原市16种PAHs的排放量约为332.10t,其中7种致癌性PAHs排放总量为35.11t.从排放源看,生活燃煤和炼焦煤是太原市排放PAHs的主要来源,占总排放量的65%以上.从各地区的PAHs排放情况看,排放量最大的地区是清徐县(87t/a),占总排放的27%.其次为古交市(54t/a)、晋源区(44t/a)、尖草坪区(40t/a).各地区人均收入与单位GDP排放量之间呈负相关(R2=0.727);各地区PAHs排放量与农村人口之间呈正相关(R2=0.813),从排放谱看,排放以低环PAHs为主(81%),致癌性PAHs占总排放量的10.6%.结果表明,太原市PAHs的排放与太原市特殊的能源结构和人群结构有关.%Sixteen types of polycyclic aromatic hydrocarbons (PAHs) were included in the priority control pollutants listed by the U.S. Environmental Protection Agency (US EPA). Herein, the emission rates and emission sources of these 16 PAHs in Taiyuan city were investigated. Results showed that the overall emission amount of the 16 PAHs in the year of 2010 in Taiyuan was 332.10t, in which 35.11t was identified as carcinogenic PAHs. Most of the PAHs were generated from the combustion of household coal and coke-production coal, accounting for 65% of the total emission amount. Among the emissions of 16 PAHs, less-ring PAHs were the majority (81%) while the carcinogenic PAHs only accounted for 10.6%. For the different districts (10 in total) in Taiyuan, the PAHs emitted from Qingxu were 87t/a, greatly more than that from Gujiao (54t/a), Jinyuan (44t/a), and Jiancaoping (40t/a). In general, there were a negative correlation between per capita income and per GDP emissions of PAHs (R2=0.727), and a positive correlation between the rural population and total PAHs emissions (R2=0.813). It was concluded that the heavy

  19. Methane Conversion to C2 Hydrocarbons Using Glow Discharge Plasma

    Institute of Scientific and Technical Information of China (English)

    HU Miao; CHEN Jierong

    2007-01-01

    The infrared emission spectra of methane, H', CH and C2 hydrocarbons in natural gas were measured. The process of methane decomposition and C2 hydrocarbons formation was investigated. The experiment showed that the time and conditions of methane decomposition and C2 hydrocarbons formation were different. Methane conversion rate increased with the increase in the current and decrease in the amount of methane. Furthermore, an examination of the reaction mechanisms revealed that free radicals played an important role in the chain reaction.

  20. Experimental determination and numerical simulation of vapor diffusion and emission in loading gasoline into tank%汽油装罐油气扩散排放的实验测定及数值模拟

    Institute of Scientific and Technical Information of China (English)

    黄维秋; 王兆利; 纪虹; 赵晨露; 吕爱华; 徐先阳; 王翊红

    2016-01-01

    It was of great significance correctly to predict the vapor diffusion and emission inside the tank for the researches of gasoline evaporation loss and vapor pollution control during the operation of loading gasoline into a tank. Then, two key parameters of the volumetric ratioλ of the displacement mixture gas of the vapor-air to the loaded gasoline and the qualitative ratioη of the evaporation loss to the loaded gasoline were mainly considered. Based on the models of volume of fluid (VOF), mass transfer and RNGk-ε turbulence, the evaporation loss was numerically simulated and experimentally investigated during the splash loading operation, and the oil vapor-air diffusion was analyzed and compared for the different loading exit heights, different loading velocity and the different initial vapor mass fraction. Meanwhile, an experimental system of evaporation loss in loading into a tank was built up to verify the numerical simulation, and the results of the numerical simulation were agreed well with the experimental data. The simulation results furthermore showed that the higher of the loading exit, the greater the qualitative ratioη of the evaporation loss to the loaded gasoline. The qualitative ratio of high exit was at around 0.34% and the qualitative ratio of low exit at around 0.025% by the increase of the loading velocity. The qualitative ratioηof high exit was at around of 0.44%, the qualitative ratio of mid exit at around 0.21% and the qualitative ratio of low exit at around 0.043% by increasing the initial vapor mass fraction. It was recommended that the effect of loading velocity and the initial vapor mass fraction should be considered in API loss formula by using a clean tank and low exit when loading and reducing loading speed appropriately before the loading pipe exit was submerged.%正确预测储油罐收油作业时罐内油气扩散排放规律对研究油品蒸发损耗及污染控制具有重要意义,因而两个关键参数(油罐排放

  1. Comparison of global 3-D aviation emissions datasets

    Directory of Open Access Journals (Sweden)

    S. C. Olsen

    2013-01-01

    Full Text Available Aviation emissions are unique from other transportation emissions, e.g., from road transportation and shipping, in that they occur at higher altitudes as well as at the surface. Aviation emissions of carbon dioxide, soot, and water vapor have direct radiative impacts on the Earth's climate system while emissions of nitrogen oxides (NOx, sulfur oxides, carbon monoxide (CO, and hydrocarbons (HC impact air quality and climate through their effects on ozone, methane, and clouds. The most accurate estimates of the impact of aviation on air quality and climate utilize three-dimensional chemistry-climate models and gridded four dimensional (space and time aviation emissions datasets. We compare five available aviation emissions datasets currently and historically used to evaluate the impact of aviation on climate and air quality: NASA-Boeing 1992, NASA-Boeing 1999, QUANTIFY 2000, Aero2k 2002, and AEDT 2006 and aviation fuel usage estimates from the International Energy Agency. Roughly 90% of all aviation emissions are in the Northern Hemisphere and nearly 60% of all fuelburn and NOx emissions occur at cruise altitudes in the Northern Hemisphere. While these datasets were created by independent methods and are thus not strictly suitable for analyzing trends they suggest that commercial aviation fuelburn and NOx emissions increased over the last two decades while HC emissions likely decreased and CO emissions did not change significantly. The bottom-up estimates compared here are consistently lower than International Energy Agency fuelburn statistics although the gap is significantly smaller in the more recent datasets. Overall the emissions distributions are quite similar for fuelburn and NOx with regional peaks over the populated land masses of North America, Europe, and East Asia. For CO and HC there are relatively larger differences. There are however some distinct differences in the altitude distribution

  2. Comparison of global 3-D aviation emissions datasets

    Directory of Open Access Journals (Sweden)

    S. C. Olsen

    2012-07-01

    Full Text Available Aviation emissions are unique from other transportation emissions, e.g., from road transportation and shipping, in that they occur at higher altitudes as well as at the surface. Aviation emissions of carbon dioxide, soot, and water vapor have direct radiative impacts on the Earth's climate system while emissions of nitrogen oxides (NOx, sulfur oxides, carbon monoxide (CO, and hydrocarbons (HC impact air quality and climate through their effects on ozone, methane, and clouds. The most accurate estimates of the impact of aviation on air quality and climate utilize three-dimensional chemistry-climate models and gridded four dimensional (space and time aviation emissions datasets. We compare five available aviation emissions datasets currently and historically used to evaluate the impact of aviation on climate and air quality: NASA-Boeing 1992, NASA-Boeing 1999, QUANTIFY 2000, Aero2k 2002, and AEDT 2006 and aviation fuel usage estimates from the International Energy Agency. Roughly 90% of all aviation emissions are in the Northern Hemisphere and nearly 60% of all fuelburn and NOx emissions occur at cruise altitudes in the Northern Hemisphere. While these datasets were created by independent methods and are thus not strictly suitable for analyzing trends they suggest that commercial aviation fuelburn and NOx emissions increased over the last two decades while HC emissions likely decreased and CO emissions did not change significantly. The bottom-up estimates compared here are consistently lower than International Energy Agency fuelburn statistics although the gap is significantly lower in the more recent datasets. Overall the emissions distributions are quite similar for fuelburn and NOx while for CO and HC there are relatively larger differences. There are however some distinct differences in the altitude distribution of emissions in certain regions for the Aero2k dataset.

  3. Water vapor release from biofuel combustion

    OpenAIRE

    Parmar, R. S.; Welling, M.; Andreae, M. O.; G. Helas

    2008-01-01

    We report on the emission of water vapor from biofuel combustion. Concurrent measurements of carbon monoxide and carbon dioxide are used to scale the concentrations of water vapor found, and are compared to carbon in the biofuel. Fuel types included hardwood (oak and African musasa), softwood (pine and spruce, partly with green needles), and African savanna grass. The session-averaged ratio of H2O to the sum of CO and CO2 in the emissions from 16 ...

  4. Emission of polycyclic aromatic hydrocarbons (PAHs and benzene, toluene, ethylbenzene and xylene (BTEX from the furan moulding sands with addition of the reclaim

    Directory of Open Access Journals (Sweden)

    M. Holtzer

    2014-10-01

    Full Text Available In this paper, the results of decomposition of a moulding sand with furfuryl resin also on a quartz matrix and with additions of a reclaimed material, under industrial conditions, are presented. Investigations of the gases emission in the test foundry plant were performed according to the original method developed in the Faculty of Foundry Engineering, AGH UST. The dependence of the emitted PAHs and BTEX group substances and ignition losses on the reclaim fraction in a moulding sand are of a linear character of a very high correlation coefficient R2. On the bases of the derived equations, it is possible to determine the amount of the emitted hazardous substances from the moulding sand containing the known fraction of the reclaim.

  5. Oxidation of gaseous hydrocarbons by alkene-utilizing bacteria

    NARCIS (Netherlands)

    Ginkel, van C.G.

    1987-01-01

    Gaseous alkenes are widespread in the environment due to the emission of these hydrocarbons by industry and due to their production from natural sources as for instance ethene by plants, fungi and bacteria. Micro-organisms have developed the potential to oxidize these hydrocarbons. Alkenes

  6. Oxidation of gaseous hydrocarbons by alkene-utilizing bacteria.

    NARCIS (Netherlands)

    Ginkel, van C.G.

    1987-01-01

    Gaseous alkenes are widespread in the environment due to the emission of these hydrocarbons by industry and due to their production from natural sources as for instance ethene by plants, fungi and bacteria. Micro-organisms have developed the potential to oxidize these hydrocarbons. Alkenes can eithe

  7. Injection of lightning-produced NOx, water vapor, wildfire emissions, and stratospheric air to the UT/LS as observed from DC3 measurements

    Science.gov (United States)

    Huntrieser, H.; Lichtenstern, M.; Scheibe, M.; Aufmhoff, H.; Schlager, H.; Pucik, T.; Minikin, A.; Weinzierl, B.; Heimerl, K.; Pollack, I. B.; Peischl, J.; Ryerson, T. B.; Weinheimer, A. J.; Honomichl, S.; Ridley, B. A.; Biggerstaff, M. I.; Betten, D. P.; Hair, J. W.; Butler, C. F.; Schwartz, M. J.; Barth, M. C.

    2016-06-01

    During the Deep Convective Clouds and Chemistry (DC3) experiment in summer 2012, airborne measurements were performed in the anvil inflow/outflow of thunderstorms over the Central U.S. by three research aircraft. A general overview of Deutsches Zentrum für Luft- und Raumfahrt (DLR)-Falcon in situ measurements (CO, O3, SO2, CH4, NO, NOx, and black carbon) is presented. In addition, a joint flight on 29 May 2012 in a convective line of isolated supercell storms over Oklahoma is described based on Falcon, National Science Foundation/National Center for Atmospheric Research Gulfstream-V (NSF/NCAR-GV), and NASA-DC8 trace species in situ and lidar measurements. During DC3 some of the largest and most destructive wildfires in New Mexico and Colorado state's history were burning, which strongly influenced air quality in the DC3 thunderstorm inflow and outflow region. Lofted biomass burning (BB) plumes were frequently observed in the mid- and upper troposphere (UT) in the vicinity of deep convection. The impact of lightning-produced NOx (LNOx) and BB emissions was analyzed on the basis of mean vertical profiles and tracer-tracer correlations (CO-NOx and O3-NO). On a regular basis DC3 thunderstorms penetrated the tropopause and injected large amounts of LNOx into the lower stratosphere (LS). Inside convection, low O3 air (~80 nmol mol-1) from the lower troposphere was rapidly transported to the UT/LS region. Simultaneously, O3-rich stratospheric air masses (~100-200 nmol mol-1) were present around and below the thunderstorm outflow and enhanced UT-O3 mixing ratios significantly. A 10 year global climatology of H2O data from the Aura Microwave Limb Sounder confirmed that the Central U.S. is a preferred region for convective injection into the LS.

  8. 蚊香燃烧过程中多环芳烃的排放特征%EMISSION CHARACTERISTICS OF POLYCYCLIC AROMATIC HYDROCARBONS FROM MOSQUITO COIL BURNING

    Institute of Scientific and Technical Information of China (English)

    周宏仓; 宋园园; 陆建刚; 李红双; 蔡华侠; 赵晓莉

    2009-01-01

    对3种类型蚊香(有烟蚊香、微烟蚊香和无烟蚊香)原料、灰烬及烟气样品经索式提取、K-D浓缩和硅胶层析纯化后,采用GC-MS分析其US EPA推荐的16种优控多环芳烃的含量.结果表明,有烟蚊香和微烟蚊香烟气中多环劳烃总含量高于原料中的含量,无烟蚊香则相反.有烟蚊香和微烟蚊香原料以3环和4环多环芳烃为主,无烟蚊香原料以2环和3环多环芳烃为主,3种类型蚊香灰烬和烟气中多环芳烃均以2环、3环和4环化合物为主.通过对比蚊香燃烧前、后样品中多环芳烃的毒性,发现同原料相比,有烟蚊香燃烧后烟气中多环芳烃的毒性显著增加,而微烟蚊香和无烟蚊香则明显减少.%For the determination of 16 priority-controlled polycyclic aromatic hydrocarbons(PAHs) recommended by US EPA in raw material, ash and smoke of three types of mosquito coils (smoke mosquito coil, micro-smoke mosquito coil and smokeless mosquito coil) by GC-MS, the samples were extracted in a Soxhlet extractor, concentrated in a K-D apparatus, and separated in a silica gel clean-up column. The results show that the total PAHs contents in the smoke are higher than those in the raw material for smoke and micro-smoke mosquito coils, while the status reverse for smokeless mosquito coil PAHs in the raw material of smoke and micro-smoke mosquito coils are dominated by 3-ring and 4-ring PAHs, while 2-ring and 3-ring PAHs are predominant in the raw material of smokeless mosquito coil. Both the ash samples and smoke samples of three mosquito coils are dominated by 2-ring, 3-ring and 4-ring PAHs. By comparison of toxic parameters between smoke and raw material of mosquito coils, the toxic equivalent of PAHs in the smoke increases obviously for smoke mosquito coil, while the status reverse for micro-smoke and smokeless mosquito coils.

  9. Microbiological aspects of the removal of chlorinated hydrocarbons from air

    NARCIS (Netherlands)

    Dolfing, Jan; Wijngaard, Arjan J. van den; Janssen, Dick B.

    1993-01-01

    Chlorinated hydrocarbons are widely used synthetic chemicals that are frequently present in industrial emissions. Bacterial degradation has been demonstrated for several components of this class of compounds. Structural features that affect the degradability include the number of chlorine atoms and

  10. Microbiological aspects of the removal of chlorinated hydrocarbons from air

    NARCIS (Netherlands)

    Dolfing, Jan; Wijngaard, Arjan J. van den; Janssen, Dick B.

    1993-01-01

    Chlorinated hydrocarbons are widely used synthetic chemicals that are frequently present in industrial emissions. Bacterial degradation has been demonstrated for several components of this class of compounds. Structural features that affect the degradability include the number of chlorine atoms and

  11. Polycyclic Aromatic Hydrocarbons

    Science.gov (United States)

    Salama, Farid

    2010-01-01

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

  12. Wetting and superhydrophobic properties of PECVD grown hydrocarbon and fluorinated-hydrocarbon coatings

    Energy Technology Data Exchange (ETDEWEB)

    Sarkar, D.K., E-mail: dsarkar@uqac.ca [Canada Research Chair on Atmospheric Icing Engineering of Power Networks (INGIVRE) and Industrial Chair on Atmospheric Icing of Power Network Equipment (CIGELE), Universite du Quebec a Chicoutimi UQAC, 555 Boulevard de l' Universite, Chicoutimi, Quebec, G7H 2B1 (Canada); Farzaneh, M. [Canada Research Chair on Atmospheric Icing Engineering of Power Networks (INGIVRE) and Industrial Chair on Atmospheric Icing of Power Network Equipment (CIGELE), Universite du Quebec a Chicoutimi UQAC, 555 Boulevard de l' Universite, Chicoutimi, Quebec, G7H 2B1 (Canada); Paynter, R.W. [INRS-EMT, 1650 boul. Lionel-Boulet, Varennes, Quebec, J3X 1S2 (Canada)

    2010-03-15

    Wetting characteristics of micro-nanorough substrates of aluminum and smooth silicon substrates have been studied and compared by depositing hydrocarbon and fluorinated-hydrocarbon coatings via plasma enhanced chemical vapor deposition (PECVD) technique using a mixture of Ar, CH{sub 4} and C{sub 2}F{sub 6} gases. The water contact angles on the hydrocarbon and fluorinated-hydrocarbon coatings deposited on silicon substrates were found to be 72 deg. and 105 deg., respectively. However, the micro-nanorough aluminum substrates demonstrated superhydrophobic properties upon coatings with fluorinated-hydrocarbon providing a water contact angle of {approx}165 deg. and contact angle hysteresis below 2 deg. with water drops rolling off from those surfaces while the same substrates showed contact angle of 135 deg. with water drops sticking on those surfaces. The superhydrophobic properties is due to the high fluorine content in the fluorinated-hydrocarbon coatings of {approx}36 at.%, as investigated by X-ray photoelectron spectroscopy (XPS), by lowering the surface energy of the micro-nanorough aluminum substrates.

  13. Study of the origin of polycyclic aromatic hydrocarbons in water of Lake Baikal

    Science.gov (United States)

    Semenova, M. Yu.; Snytko, V. A.; Marinaite, I. I.

    2017-06-01

    The concentration of polycyclic aromatic hydrocarbons in the water of Lake Baikal is estimated. The published data on the composition of polycyclic aromatic hydrocarbons in industrial and communal emissions and in crude oils are analyzed. Anthropogenic sources of lake water contamination are revealed. It is concluded that polycyclic aromatic hydrocarbons enter the lake as a result of natural oil release.

  14. Method for producing diene hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Tsaylingol' d, A.L.; Abayev, G.N.; Mikhaylov, R.K.; Stepanov, G.A.; Troitskiy, A.P.

    1980-04-28

    A method is claimed for producing diene hydrocarbons by oxidational dehydration of paraffin or olefin hydrocarbons in a fluidized bed of a concentrate with circulation of the latter between the zones of the reaction of regeneration with the help of circulation stand pipes. To increase the efectiveness of the process, it is proposed to circulate the concentrate between the zones of reaction and regeneration, sequentially disposed in a common apparatus with a difference in the concentration of the concentrate in the circulation stand pipes disposed in the same apparatus and the zone of the reaction equal to 20-700 kg/m/sup 3/. For example, the process of oxidational dehydration of butane through the proposed system is conducted in an apparatus with a diameter of 1,000 mm, a circulation stand pipe diameter of 500 mm, a linear gas speed in the reaction zone of 0.6 m/s, and in the circulation stand pipe of 0.15 m/s. The concentration of the concentrate in the dehydration zone is 640 kg/m/sup 3/ and in the stand pipe, 970 kg/m/sup 3/. The volumetric ratio of the n-C/sub 4/H/sub 10/:air, air:vapor vapor in the form of a condensate is 1:7.2:4.5:5.5. The output of the butadiene is: in the passed butane, 32.9% and in the broken down butane, 52.5%. The butane conversion is 62.6%. The losses of the concentrate with the contact gas and with the regeneration gases is 1/3 as much for the supplied butane, than in a known method. The method makes it possible to reduce the air expenditure by 60%, to reduce the concentrate losses by 2-3 times and to simplify the industrial system.

  15. Receptor Model Source Apportionment of Nonmethane Hydrocarbons in Mexico City

    Directory of Open Access Journals (Sweden)

    V. Mugica

    2002-01-01

    Full Text Available With the purpose of estimating the source contributions of nonmethane hydrocarbons (NMHC to the atmosphere at three different sites in the Mexico City Metropolitan Area, 92 ambient air samples were measured from February 23 to March 22 of 1997. Light- and heavy-duty vehicular profiles were determined to differentiate the NMHC contribution of diesel and gasoline to the atmosphere. Food cooking source profiles were also determined for chemical mass balance receptor model application. Initial source contribution estimates were carried out to determine the adequate combination of source profiles and fitting species. Ambient samples of NMHC were apportioned to motor vehicle exhaust, gasoline vapor, handling and distribution of liquefied petroleum gas (LP gas, asphalt operations, painting operations, landfills, and food cooking. Both gasoline and diesel motor vehicle exhaust were the major NMHC contributors for all sites and times, with a percentage of up to 75%. The average motor vehicle exhaust contributions increased during the day. In contrast, LP gas contribution was higher during the morning than in the afternoon. Apportionment for the most abundant individual NMHC showed that the vehicular source is the major contributor to acetylene, ethylene, pentanes, n-hexane, toluene, and xylenes, while handling and distribution of LP gas was the major source contributor to propane and butanes. Comparison between CMB estimates of NMHC and the emission inventory showed a good agreement for vehicles, handling and distribution of LP gas, and painting operations; nevertheless, emissions from diesel exhaust and asphalt operations showed differences, and the results suggest that these emissions could be underestimated.

  16. Hydrocarbons in coastal sediments from the Mediterranean sea (Gulf of Fos area, France).

    Science.gov (United States)

    Mille, Gilbert; Asia, Laurence; Guiliano, Michel; Malleret, Laure; Doumenq, Pierre

    2007-05-01

    Sedimentary hydrocarbons have been studied quantitatively and qualitatively in 11 coastal stations located in the Gulf of Fos (French Mediterranean coast). Hydrocarbon levels ranged from 10 to 260 mg kg(-1) sed. dry weight. A new parameter "NAR" (Natural n-alkane ratio) is proposed to evaluate the contribution of terrestrial inputs of hydrocarbons in the sediments. The origins of hydrocarbons are multiple: terrestrial inputs, biogenic, pyrolytic (industry emissions mainly steel and iron industries, ship and road traffic). Generally, the main source of contamination is not petroleum. Several ratios between parent polycyclic aromatic hydrocarbons show that the sources of hydrocarbons in the sediments are generally much more pyrolytic than petrogenic.

  17. Reduction of the thickness of the boundary film at rectification of hydrocarbonic mixes with application of dry distillation

    Directory of Open Access Journals (Sweden)

    Zakirjan Salimov

    2011-11-01

    Full Text Available The paper describes a negative impact of water vapor from the distillation of hydrocarbon mixtures. It is substantiated a promising method of primary distillation process for oil and raw materials.

  18. Novel Photocatalytic Reactor Development for Removal of Hydrocarbons from Water

    Directory of Open Access Journals (Sweden)

    Morgan Adams

    2008-01-01

    Full Text Available Hydrocarbons contamination of the marine environment generated by the offshore oil and gas industry is generated from a number of sources including oil contaminated drill cuttings and produced waters. The removal of hydrocarbons from both these sources is one of the most significant challenges facing this sector as it moves towards zero emissions. The application of a number of techniques which have been used to successfully destroy hydrocarbons in produced water and waste water effluents has previously been reported. This paper reports the application of semiconductor photocatalysis as a final polishing step for the removal of hydrocarbons from two waste effluent sources. Two reactor concepts were considered: a simple flat plate immobilised film unit, and a new rotating drum photocatalytic reactor. Both units proved to be effective in removing residual hydrocarbons from the effluent with the drum reactor reducing the hydrocarbon content by 90% under 10 minutes.

  19. 我国8种市售蚊香燃烧烟气中多环芳烃的排放特征%Emission Characteristics of Polycyclic Aromatic Hydrocarbons in the Smoke from Eight Mosquito Coils in Chinese Market

    Institute of Scientific and Technical Information of China (English)

    周宏仓; 宋园园; 陆建刚; 李红双; 马嫣; 蔡华侠; 赵晓莉

    2009-01-01

    利用GC-MS对8种具有代表性的市售蚊香燃烧烟气中16种列入美国环境保护署(US EPA)优先控制的多环芳烃(PAHs)进行分析. 结果表明:有烟蚊香烟气中16种优先控制的PAHs均有检出(6号蚊香除外),排放因子较大的化合物主要有萘、苊、二氢苊、菲和荧蒽;无烟蚊香烟气中仅检出10~11种,排放因子最大的化合物是菲,其次为萘;各种蚊香烟气中PAHs均以2~3环化合物为主,约占排放量的83.3%~98.0%. 同无烟蚊香相比,有烟蚊香烟气中PAHs的排放量较大,毒性也较高. 根据烟气中PAHs排放因子估算出一盘蚊香燃烧后烟气中苯并[a]芘排放量相当于燃烧4支香烟,PAHs排放量相当于燃烧8支香烟;蚊香燃烧后室内空气中ρ(PAHs)高达 1 486.60ng/m~3,其中ρ(苯并[a]芘)为8.07ng/m~3,超过其 (GB/T18883─2002)中的日均限值.%The GC-MS technique was applied to analyze 16 US EPA-recommend priority-controlled polycyclic aromatic hydrocarbons (PAHs) from the smoke of eight mosquito coils in Chinese market. The results showed that all 16 priority-controlled PAHs were detected in the smoke of all smoking mosquito coils with the exception of coil No.6. The emissions were characterized by the predominance of Nap, AcPy, AcP, Phe and FluA. Only 10-11 PAHs were detected in the smoke from smokeless mosquito coils, with the main contributors including Phe and NaP. Among all the coils, the concentration distribution of PAHs was dominated by 2-ringed and 3-ringed PAHs, accounting for about 83.3%-98.0%. It can be seen that the amount of total PAHs emission and total toxic equivalent of PAHs in the smoke from smoking mosquito coils is much higher than that from smokeless mosquito coils. Based on emission factors in the smoke, burning one mosquito coil would release the same amount of BaP as burning 4 cigarettes, and the total amount of PAHs emission from burning one mosquito coil would be as high as that released from burning 8 cigarettes

  20. Development of Advanced Membranes Technology Platform for Hydrocarbon Separations

    Energy Technology Data Exchange (ETDEWEB)

    Kalthod, Dr Dilip [Air Products and Chemicals, Inc., St. Louis, MO (United States)

    2010-03-01

    Virtually all natural gas is dehydrated during its production, transmission and storage, mostly by absorption processes. Membranes offer many potential advantages over absorption, including smaller footprints, lighter-weight packages, packaging flexibility, minimal electrical power duty, amenability to expansion due to system modularity, reduced maintenance costs, reduced emissions of heavy hydrocarbons, no liquid waste streams, and amenability to unmanned operation. The latter is particularly valuable because new natural gas sources are generally located in remote onshore and offshore sites. Most commercially-available membranes for natural gas upgrading involve high capital costs, high methane loss and performance degradation from operational upsets – all of which are barriers to their widespread adoption by the industry. The original focus of the project was to develop and demonstrate robust, high-performance membranes for natural gas dehydration. The first task completed was a user needs-and-wants study to 1) clarify the expectations of system fabricators and end users of the new separations equipment, and 2) establish the required technical and commercial targets for the membrane products. Following this, membrane system modeling and membrane development in the lab proceeded in parallel. Membrane module diameter and length, as well as and the fiber outer and inner fiber diameter, were optimized from a mathematical model that accounts for the relevant fluid dynamics and permeation phenomena. Module design was evaluated in the context of overall system design, capital costs and energy consumption, including the process scheme (particularly sweep generation), feed pretreatment, system layout, and process control. This study provided targets for membrane permeation coefficients and membrane geometry in a commercial offering that would be competitive with absorption systems. A commercially-available polymer with good tensile strength and chemical resistance was

  1. Knock Resistance and Fine Particle Emissions for Several Biomass-Derived Oxygenates in a Direct-Injection Spark-Ignition Engine

    Energy Technology Data Exchange (ETDEWEB)

    Ratcliff, Matthew A.; Burton, Jonathan; Sindler, Petr; Christensen, Earl; Fouts, Lisa; Chupka, Gina M.; McCormick, Robert L.

    2016-04-01

    Several high octane number oxygenates that could be derived from biomass were blended with gasoline and examined for performance properties and their impact on knock resistance and fine particle emissions in a single cylinder direct-injection spark-ignition engine. The oxygenates included ethanol, isobutanol, anisole, 4-methylanisole, 2-phenylethanol, 2,5-dimethyl furan, and 2,4-xylenol. These were blended into a summertime blendstock for oxygenate blending at levels ranging from 10 to 50 percent by volume. The base gasoline, its blends with p-xylene and p-cymene, and high-octane racing gasoline were tested as controls. Relevant gasoline properties including research octane number (RON), motor octane number, distillation curve, and vapor pressure were measured. Detailed hydrocarbon analysis was used to estimate heat of vaporization and particulate matter index (PMI). Experiments were conducted to measure knock-limited spark advance and particulate matter (PM) emissions. The results show a range of knock resistances that correlate well with RON. Molecules with relatively low boiling point and high vapor pressure had little effect on PM emissions. In contrast, the aromatic oxygenates caused significant increases in PM emissions (factors of 2 to 5) relative to the base gasoline. Thus, any effect of their oxygen atom on increasing local air-fuel ratio was outweighed by their low vapor pressure and high double-bond equivalent values. For most fuels and oxygenate blend components, PMI was a good predictor of PM emissions. However, the high boiling point, low vapor pressure oxygenates 2-phenylethanol and 2,4-xylenol produced lower PM emissions than predicted by PMI. This was likely because they did not fully evaporate and combust, and instead were swept into the lube oil.

  2. Health assessment of gasoline and fuel oxygenate vapors: subchronic inhalation toxicity.

    Science.gov (United States)

    Clark, Charles R; Schreiner, Ceinwen A; Parker, Craig M; Gray, Thomas M; Hoffman, Gary M

    2014-11-01

    Sprague Dawley rats were exposed via inhalation to vapor condensates of either gasoline or gasoline combined with various fuel oxygenates to assess whether their use in gasoline influences the hazard of evaporative emissions. Test substances included vapor condensates prepared from an EPA described "baseline gasoline" (BGVC), or gasoline combined with methyl tertiary butyl ether (G/MTBE), ethyl t-butyl ether (G/ETBE), t-amyl methyl ether (G/TAME), diisopropyl ether (G/DIPE), ethanol (G/EtOH), or t-butyl alcohol (G/TBA). Target concentrations were 0, 2000, 10,000 or 20,000mg/m(3) and exposures were for 6h/day, 5days/week for 13weeks. A portion of the animals were maintained for a four week recovery period to determine the reversibility of potential adverse effects. Increased kidney weight and light hydrocarbon nephropathy (LHN) were observed in treated male rats in all studies which were reversible or nearly reversible after 4weeks recovery. LHN is unique to male rats and is not relevant to human toxicity. The no observed effect level (NOAEL) in all studies was 10,000mg/m(3), except for G/MTBE (gasoline alone.

  3. Water vapor release from biomass combustion

    OpenAIRE

    Parmar, R. S.; Welling, M.; Andreae, M. O.; G. Helas

    2008-01-01

    We report on the emission of water vapor from biomass combustion. Concurrent measurements of carbon monoxide and carbon dioxide are used to scale the concentrations of water vapor found, and are referenced to carbon in the biomass. The investigated fuel types include hardwood (oak and African musasa), softwood (pine and spruce, partly with green needles), and African savanna grass. The session-averaged ratio of H2O to the sum of CO and CO2 in the ...

  4. A source study of atmospheric polycyclic aromatic hydrocarbons in Shenzhen, South China.

    Science.gov (United States)

    Liu, Guoqing; Tong, Yongpeng; Luong, John H T; Zhang, Hong; Sun, Huibin

    2010-04-01

    Air pollution has become a serious problem in the Pearl River Delta, South China, particularly in winter due to the local micrometeorology. In this study, atmospheric polycyclic aromatic hydrocarbons (PAHs) were monitored weekly in Shenzhen during the winter of 2006. Results indicated that the detected PAHs were mainly of vapor phase compounds with phenanthrene dominant. The average vapor phase and particle phase PAHs concentration in Shenzhen was 101.3 and 26.7 ng m( - 3), respectively. Meteorological conditions showed great effect on PAH concentrations. The higher PAHs concentrations observed during haze episode might result from the accumulation of pollutants under decreased boundary layer, slower wind speed, and long-term dryness conditions. The sources of PAHs in the air were estimated by principal component analysis in combination with diagnostic ratios. Vehicle exhaust was the major PAHs source in Shenzhen, accounting for 50.0% of the total PAHs emissions, whereas coal combustion and solid waste incineration contributed to 29.4% and 20.6% of the total PAHs concentration, respectively. The results clearly indicated that the increasing solid waste incinerators have become a new important PAHs source in this region.

  5. Oxygenated Derivatives of Hydrocarbons

    Science.gov (United States)

    For the book entitled “Insect Hydrocarbons: Biology, Biochemistry and Chemical Ecology”, this chapter presents a comprehensive review of the occurrence, structure and function of oxygenated derivatives of hydrocarbons. The book chapter focuses on the occurrence, structural identification and functi...

  6. Hydrocarbon Spectral Database

    Science.gov (United States)

    SRD 115 Hydrocarbon Spectral Database (Web, free access)   All of the rotational spectral lines observed and reported in the open literature for 91 hydrocarbon molecules have been tabulated. The isotopic molecular species, assigned quantum numbers, observed frequency, estimated measurement uncertainty and reference are given for each transition reported.

  7. Plasma devices for hydrocarbon reformation

    KAUST Repository

    Cha, Min Suk

    2017-02-16

    Plasma devices for hydrocarbon reformation are provided. Methods of using the devices for hydrocarbon reformation are also provided. The devices can include a liquid container to receive a hydrocarbon source, and a plasma torch configured to be submerged in the liquid. The plasma plume from the plasma torch can cause reformation of the hydrocarbon. The device can use a variety of plasma torches that can be arranged in a variety of positions in the liquid container. The devices can be used for the reformation of gaseous hydrocarbons and/or liquid hydrocarbons. The reformation can produce methane, lower hydrocarbons, higher hydrocarbons, hydrogen gas, water, carbon dioxide, carbon monoxide, or a combination thereof.

  8. Prediction of vapor pressure and heats of vaporization of edible oil/fat compounds by group contribution

    DEFF Research Database (Denmark)

    Ceriani, Roberta; Gani, Rafiqul; Liu, Y.A.

    2013-01-01

    databank (2036 values) composed by fatty compounds, i.e., fatty acids, methyl-, ethyl-, propyl- and butyl- esters, fatty alcohols, tri-, di- and monoacylglycerols and hydrocarbons. This new methodology gives improved predictions when compared to a prior group contribution equation (Ceriani and Meirelles......, 2004) due to the inclusion of new experimental data for fatty esters and partial acylglycerols (besides hydrocarbons) and critical points, and a new temperature dependency. Heats of vaporization are properly described as a function of reduced temperature up to the critical condition....

  9. Possible seasonal variability of mesospheric water vapor

    Science.gov (United States)

    Bevilacqua, R. M.; Schwartz, P. R.; Wilson, W. J.; Ricketts, W. B.; Howard, R. J.

    1985-01-01

    Ground-based spectral line measurements of the 22.2 GHz water vapor line in atmospheric emission were made at the Jet Propulsion Laboratory, which have been used to deduce the mesospheric water vapor profile. The measurements were made nearly continuously in the spring and early summer of 1984. The results indicate a temporal increase in the water vapor mixing ratio in the upper mesosphere from April through June. At 75 km, this increase is nearly by a factor of 2. Comparison of the present results with the results of a similar series of measurements made at the Haystack (radio astronomy) Observatory indicate that this temporal increase is part of a seasonal variation.

  10. Monitoring laboratory-scale bioventing using synchronous scan fluorescence spectroscopy: analysis of the vapor phase.

    Science.gov (United States)

    Bachman, J; Kanan, S M; Patterson, H H

    2001-01-01

    Bioventing is an improved method of soil remediation that is being used with increasing frequency. In this paper, we refine techniques to measure the progress of petroleum hydrocarbon decomposition by monitoring vapor phase composition with synchronous scan fluorescence spectroscopy (SSFS). Analysis of the vapor phase has advantages compared to standard extraction techniques that require extensive sample handling and clean up. For comparison, hydrocarbon contamination in the soil was measured by analysis of Soxhlet extractions with gas chromatography-mass spectrometry (GC-MS). Comparison of the GC-MS and SSFS data showed that changes in hydrocarbon composition measured in the vapor phase provide an accurate measure of decomposition reactions taking place in the soil.

  11. Measurements and source apportionment of particle-associated polycyclic aromatic hydrocarbons in ambient air in Riyadh, Saudi Arabia

    Science.gov (United States)

    Bian, Qijing; Alharbi, Badr; Collett, Jeffrey; Kreidenweis, Sonia; Pasha, Mohammad J.

    2016-07-01

    Ambient air samples were obtained in Riyadh, the capital and largest city of Saudi Arabia, during two measurement campaigns spanning September 2011 to September 2012. Sixteen particle-phase polycyclic aromatic hydrocarbons (PAH) were quantified in 167 samples. Pyrene and fluoranthene were the most abundant PAH, with average of 3.37 ± 14.01 ng m-3 and 8.00 ± 44.09 ng m-3, respectively. A dominant contribution from low molecular weight (LMW) PAH (MW < 228) suggested a large influence of industrial emissions on PAH concentrations. Monte Carlo source apportionment using diagnostic ratios showed that 80 ± 10% of the average LMW PAH concentrations were contributed by petroleum vapor emissions, while 53 ± 19% of high molecular weight (HMW) PAH were from solid fuel combustion emissions. The positive matrix factorization model estimated that oil combustion emissions dominated total PAH concentrations, accounting for on average 96%, likely due to widespread use of oil fuels in energy production (power plants and industries). Our results demonstrate the significant influence of petroleum product production and consumption on particulate-phase PAH concentrations in Riyadh, but also point to the importance of traffic and solid fuel burning, including coke burning and seasonal biomass burning, especially as they contribute to the ambient levels of HMW PAH.

  12. Load-Dependent Emission Factors and Chemical Characteristics of IVOCs from a Medium-Duty Diesel Engine.

    Science.gov (United States)

    Cross, Eben S; Sappok, Alexander G; Wong, Victor W; Kroll, Jesse H

    2015-11-17

    A detailed understanding of the climate and air quality impacts of mobile-source emissions requires the characterization of intermediate-volatility organic compounds (IVOCs), relatively-low-vapor-pressure gas-phase species that may generate secondary organic aerosol with high yields. Due to challenges associated with IVOC detection and quantification, IVOC emissions remain poorly understood at present. Here, we describe measurements of the magnitude and composition of IVOC emissions from a medium-duty diesel engine. Measurements are made on an engine dynamometer and utilize a new mass-spectrometric instrument to characterize the load dependence of the emissions in near-real-time. Results from steady-state engine operation indicate that IVOC emissions are highly dependent on engine power, with highest emissions at engine idle and low-load operation (≤25% maximum rated power) with a chemical composition dominated by saturated hydrocarbon species. Results suggest that unburned fuel components are the dominant IVOCs emitted at low loads. As engine load increases, IVOC emissions decline rapidly and become increasingly characterized by unsaturated hydrocarbons and oxygenated organics, newly formed from incomplete combustion processes at elevated engine temperatures and pressures. Engine transients, including a cold-start ignition and engine acceleration, show IVOC emission profiles that are different in amount or composition compared to steady-state combustion, underscoring the utility of characterizing IVOC emissions with high time resolution across realistic engine operating conditions. We find possible evidence for IVOC losses on unheated dilution and sampling surfaces, which need to be carefully accounted for in IVOC emission studies.

  13. Formation of polycyclic aromatic hydrocarbons and soot in fuel-rich oxidation of methane in a laminar flow reactor

    DEFF Research Database (Denmark)

    Skjøth-Rasmussen, Martin Skov; Glarborg, Peter; Østberg, M.

    2004-01-01

    Conversion of methane to higher hydrocarbons, polycyclic aromatic hydrocarbons (PAHs), and soot was investigated under fuel-rich conditions in a laminar flow reactor. The effects of stoichiometry, dilution, and water vapor addition were studied at temperatures between 1073 and 1823 K. A chemical...... decrease with increasing addition of water vapor. The effect is described qualitatively by the reaction mechanism. The enhanced oxidation of acetylene is attributed to higher levels of hydroxyl radicals, formed from the reaction between the water vapor and hydrogen atoms....

  14. AMTEC vapor-vapor series connected cells

    Science.gov (United States)

    Underwood, Mark L.; Williams, Roger M.; Ryan, Margaret A.; Nakamura, Barbara J.; Oconnor, Dennis E.

    1995-08-01

    An alkali metal thermoelectric converter (AMTEC) having a plurality of cells structurally connected in series to form a septum dividing a plenum into two chambers, and electrically connected in series, is provided with porous metal anodes and porous metal cathodes in the cells. The cells may be planar or annular, and in either case a metal alkali vapor at a high temperature is provided to the plenum through one chamber on one side of the wall and returned to a vapor boiler after condensation at a chamber on the other side of the wall in the plenum. If the cells are annular, a heating core may be placed along the axis of the stacked cells. This arrangement of series-connected cells allows efficient generation of power at high voltage and low current.

  15. Atmospheric Hydrodeoxygenation of Biomass Fast Pyrolysis Vapor by MoO3

    DEFF Research Database (Denmark)

    Zhou, Guofeng; Jensen, Peter Arendt; Le, Duy Michael

    2016-01-01

    MoO3 has been tested as a catalyst in hydrodeoxygenation (HDO) of both model compounds (acetone and guaiacol) and real biomass pyrolysis vapors under atmospheric pressure. The pyrolysis vapor was obtained by fast pyrolysis of wood or lignin in a continuous fast pyrolysis reactor at a fixed...... temperature of 500 °C, and it subsequently passed through a downstream, close coupled, fixed bed reactor containing the MoO3 catalyst. The influences of the catalyst temperature and the concentration of H2 on the HDO of the pyrolysis vapors were investigated. The level of HDO of the biomass pyrolysis vapors...... was not significant at temperatures below 400 °C. At 450 °C catalyst temperature and 93 vol % H2 concentration, the wood pyrolysis vapor was more active toward cracking forming gas species instead of performing the desired HDO forming hydrocarbons. The lignin pyrolysis vapor was more resistant to cracking and yielded...

  16. Vapor Control Layer Recommendations

    Energy Technology Data Exchange (ETDEWEB)

    None

    2009-09-08

    This information sheet describes the level of vapor control required on the interior side of framed walls with typical fibrous cavity insulation (fibreglass, rockwool, or cellulose, based on DOE climate zone of construction.

  17. Air-dust-borne associations of phototrophic and hydrocarbon-utilizing microorganisms: promising consortia in volatile hydrocarbon bioremediation.

    Science.gov (United States)

    Al-Bader, Dhia; Eliyas, Mohamed; Rayan, Rihab; Radwan, Samir

    2012-11-01

    Aquatic and terrestrial associations of phototrophic and heterotrophic microorganisms active in hydrocarbon bioremediation have been described earlier. The question arises: do similar consortia also occur in the atmosphere? Dust samples at the height of 15 m were collected from Kuwait City air, and analyzed microbiologically for phototrophic and heterotrophic hydrocarbon-utilizing microorganisms, which were subsequently characterized according to their 16S rRNA gene sequences. The hydrocarbon utilization potential of the heterotrophs alone, and in association with the phototrophic partners, was measured quantitatively. The chlorophyte Gloeotila sp. and the two cyanobacteria Nostoc commune and Leptolyngbya thermalis were found associated with dust, and (for comparison) the cynobacteria Leptolyngbya sp. and Acaryochloris sp. were isolated from coastal water. All phototrophic cultures harbored oil vapor-utilizing bacteria in the magnitude of 10(5) g(-1). Each phototrophic culture had its unique oil-utilizing bacteria; however, the bacterial composition in Leptolyngbya cultures from air and water was similar. The hydrocarbon-utilizing bacteria were affiliated with Acinetobacter sp., Aeromonas caviae, Alcanivorax jadensis, Bacillus asahii, Bacillus pumilus, Marinobacter aquaeolei, Paenibacillus sp., and Stenotrophomonas maltophilia. The nonaxenic cultures, when used as inocula in batch cultures, attenuated crude oil in light and dark, and in the presence of antibiotics and absence of nitrogenous compounds. Aqueous and diethyl ether extracts from the phototrophic cultures enhanced the growth of the pertinent oil-utilizing bacteria in batch cultures, with oil vapor as a sole carbon source. It was concluded that the airborne microbial associations may be effective in bioremediating atmospheric hydrocarbon pollutants in situ. Like the aquatic and terrestrial habitats, the atmosphere contains dust-borne associations of phototrophic and heterotrophic hydrocarbon

  18. Thraustochytrid protists degrade hydrocarbons

    Digital Repository Service at National Institute of Oceanography (India)

    Raikar, M.T.; Raghukumar, S.; Vani, V.; David, J.J.; Chandramohan, D.

    Although thraustochytrid protists are known to be of widespread occurrence in the sea, their hydrocarbon-degrading abilities have never been investigated. We isolated thraustochytrids from coastal waters and sediments of Goa coast by enriching MPN...

  19. Tungsten chemical vapor deposition method

    Energy Technology Data Exchange (ETDEWEB)

    Hirano, Kiichi; Takeda, Nobuo.

    1993-07-13

    A tungsten chemical vapor deposition method is described, comprising: a first step of selectively growing a first thin tungsten film of a predetermined thickness in a desired region on the surface of a silicon substrate by reduction of a WF[sub 6] gas introduced into an atmosphere of a predetermined temperature containing said silicon substrate; and a second step of selectively growing a second tungsten film of a predetermined thickness on said first thin tungsten film by reduction of said WF[sub 6] with a silane gas further introduced into said atmosphere, wherein the surface state of said substrate is monitored by a pyrometer and the switching from said first step to said second step is performed when the emissivity of infrared light from the substrate surfaces reaches a predetermined value.

  20. Water vapor release from biomass combustion

    Directory of Open Access Journals (Sweden)

    R. S. Parmar

    2008-10-01

    Full Text Available We report on the emission of water vapor from biomass combustion. Concurrent measurements of carbon monoxide and carbon dioxide are used to scale the concentrations of water vapor found, and are referenced to carbon in the biomass. The investigated fuel types include hardwood (oak and African musasa, softwood (pine and spruce, partly with green needles, and African savanna grass. The session-averaged ratio of H2O to the sum of CO and CO2 in the emissions from 16 combustion experiments ranged from 1.2 to 3.7, indicating the presence of water that is not chemically bound. This non-bound biomass moisture content ranged from 33% in the dry African hardwood, musasa, to 220% in fresh pine branches with needles. The moisture content from fresh biomass contributes significantly to the water vapor in biomass burning emissions, and its influence on the behavior of fire plumes and pyro-cumulus clouds needs to be evaluated.

  1. Metabolism of Benzene, Toluene, and Xylene Hydrocarbons in Soil†

    OpenAIRE

    Tsao, C.-W.; Song, H. -G.; Bartha, R

    1998-01-01

    Enrichment cultures obtained from soil exposed to benzene, toluene, and xylene (BTX) mineralized benzene and toluene but cometabolized only xylene isomers, forming polymeric residues. This observation prompted us to investigate the metabolism of 14C-labeled BTX hydrocarbons in soil, either individually or as mixtures. BTX-supplemented soil was incubated aerobically for up to 4 weeks in a sealed system that automatically replenished any O2 consumed. The decrease in solvent vapors and the produ...

  2. Vaporization characteristics of carbon heat shields under radiative heating.

    Science.gov (United States)

    Davy, W. C.; Bar-Nun, A.

    1972-01-01

    Study of the vaporization characteristics of samples of ATJ graphite, a material that has been considered for use on a Jovian probe. These samples were subjected to radiative heating loads of approximately 2 kW/sq cm in argon atmospheres of pressures from 0.00046 to 1 atm. Surface temperatures, mass loss rates, and spatially resolved emission spectral data were recorded. These data are analyzed to determine carbon vapor pressure as a function of temperature and are compared with current models for the vapor pressure of carbon. The effects of finite vaporization (i.e., nonequilibrium) rates are considered and compared with experiment. Estimates of the heat of vaporization from an energy balance are also presented.

  3. Green Methodologies to Test Hydrocarbon Reservoirs

    Directory of Open Access Journals (Sweden)

    Francesca Verga

    2010-01-01

    Full Text Available Problem statement: The definition and the economic viability of the best development strategy of a hydrocarbon reservoir mainly depend on the quantity and type of fluids and on the well productivity. Well testing, consisting in producing hydrocarbon to the surface while measuring the pressure variations induced in the reservoir, has been used for decades to determine the fluid nature and well potential. In exploration and appraisal scenarios the hydrocarbons produced during a test are flared, contributing to the emissions of greenhouse gases. Approach: Due to more stringent environmental regulations and a general need for reduced operating expenses, the current industry drivers in today’s formation evaluation methodologies demand short, safe, cost-effective and environmentally friendly test procedures, especially when conventional tests are prohibitively expensive, logistically not feasible or no surface emissions are allowed. Different methods have been proposed or resuscitated in the last years, such as wireline formation tests, closed chamber tests, production/reinjection tests and injection tests, as viable alternatives to conventional well testing. Results: While various short-term tests, test procedures and interpretation methods are apparently available for conducting successful tests without hydrocarbon production at the surface, clarity is lacking for specific applications of these techniques. An attempt to clarify advantages and limitations of each methodology, particularly with respect to the main testing target is pursued in this study. Specific insight is provided on injection testing, which is one of the most promising methodology to replace traditional well testing in reservoir characterization, except for the possibility to sample the formation fluids. Conclusion/Recommendations: Not a single one method but a combination of more methodologies, in particular injection testing and wireline formation testing, is the most promising

  4. Three Dimensional Vapor Intrusion Modeling: Model Validation and Uncertainty Analysis

    Science.gov (United States)

    Akbariyeh, S.; Patterson, B.; Rakoczy, A.; Li, Y.

    2013-12-01

    Volatile organic chemicals (VOCs), such as chlorinated solvents and petroleum hydrocarbons, are prevalent groundwater contaminants due to their improper disposal and accidental spillage. In addition to contaminating groundwater, VOCs may partition into the overlying vadose zone and enter buildings through gaps and cracks in foundation slabs or basement walls, a process termed vapor intrusion. Vapor intrusion of VOCs has been recognized as a detrimental source for human exposures to potential carcinogenic or toxic compounds. The simulation of vapor intrusion from a subsurface source has been the focus of many studies to better understand the process and guide field investigation. While multiple analytical and numerical models were developed to simulate the vapor intrusion process, detailed validation of these models against well controlled experiments is still lacking, due to the complexity and uncertainties associated with site characterization and soil gas flux and indoor air concentration measurement. In this work, we present an effort to validate a three-dimensional vapor intrusion model based on a well-controlled experimental quantification of the vapor intrusion pathways into a slab-on-ground building under varying environmental conditions. Finally, a probabilistic approach based on Monte Carlo simulations is implemented to determine the probability distribution of indoor air concentration based on the most uncertain input parameters.

  5. Quality Assurance Project Plan for waste tank vapor characterization

    Energy Technology Data Exchange (ETDEWEB)

    Suydam, C.D. Jr.

    1993-12-01

    This Quality Assurance Project Plan, WHC-SD-WM-QAPP-013, applies to four separate vapor sampling tasks associated with Phases 1 and 2 of the Tank Vapor Issue Resolution Program and support of the Rotary Mode Core Drilling Portable Exhauster Permit. These tasks focus on employee safety concerns and tank ventilation emission control design requirements. Previous characterization efforts and studies are of insufficient accuracy to adequately define the problem. It is believed that the technology and maturity of sampling and analytical methods can be sufficiently developed to allow the characterization of the constituents of the tank vapor space.

  6. Synthesis of hydrocarbon fluid inclusions at low temperature

    Energy Technology Data Exchange (ETDEWEB)

    Pironon, J. (Centre de Recherche sur la Geologie de l' Uranium and GS-CNRS CREGU, Vandoeuvre-les-Nancy (France))

    Hydrocarbon fluid inclusions have been synthesized in halogenide and sulfate crystals at low temperature (<100C) and atmospheric pressure. Water-immiscible hydrocarbon droplets were either trapped separately or with an aqueous and/or a vapor phase. Impurities on the crystal surface were verified by infrared microspectrometry, and the similarity between the initial liquid and the liquid trapped in the inclusion was documented by Raman microspectrometry for nonfluorescent compounds. This inclusion type represents a new tool for understanding inclusion-formation phenomena and for the calibration of techniques used in hydrocarbon fluid-inclusion analysis ({mu}FT-IR, {mu}Raman, {mu}UV-fluorescence, gas chromatography, mass spectrometry); these inclusions allow one to obtain microthermometric calibration curves with a high precision at low temperature.

  7. Vapor pressures and enthalpies of vaporization of azides

    Energy Technology Data Exchange (ETDEWEB)

    Verevkin, Sergey P., E-mail: sergey.verevkin@uni-rostock.de [Department of Physical Chemistry, University of Rostock, Dr-Lorenz-Weg 1, D-18059 Rostock (Germany); Emel' yanenko, Vladimir N. [Department of Physical Chemistry, University of Rostock, Dr-Lorenz-Weg 1, D-18059 Rostock (Germany); Algarra, Manuel [Centro de Geologia do Porto, Faculdade de Ciencias, Universidade do Porto, Rua do Campo Alegre 687, 4169-007 Porto (Portugal); Manuel Lopez-Romero, J. [Department of Organic Chemistry, University of Malaga. Campus de Teatinos s/n, 29071 Malaga (Spain); Aguiar, Fabio; Enrique Rodriguez-Borges, J.; Esteves da Silva, Joaquim C.G. [Centro de Investigacao em Quimica (CIQ-UP), Faculdade de Ciencias da Universidade do Porto, Rua do Campo Alegre 687, 4169-007 Porto (Portugal)

    2011-11-15

    Highlights: > We prepared and measured vapor pressures and vaporization enthalpies of 7 azides. > We examined consistency of new and available in the literature data. > Data for geminal azides and azido-alkanes selected for thermochemical calculations. - Abstract: Vapor pressures of some azides have been determined by the transpiration method. The molar enthalpies of vaporization {Delta}{sub l}{sup g}H{sub m} of these compounds were derived from the temperature dependencies of vapor pressures. The measured data sets were successfully checked for internal consistency by comparison with vaporization enthalpies of similarly structured compounds.

  8. Thermochemical properties and phase behavior of halogenated polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Fu, Jinxia; Suuberg, Eric M

    2012-03-01

    Knowledge of vapor pressure of organic pollutants is essential in predicting their fate and transport in the environment. In the present study, the vapor pressures of 12 halogenated polycyclic aromatic compounds (PACs), 9-chlorofluorene, 2,7-dichlorofluorene, 2-bromofluorene, 9-bromofluorene, 2,7-dibromofluorene, 2-bromoanthracene, 9-chlorophenanthrene, 9-bromophenanthrene, 9,10-dibromophenanthrene, 1-chloropyrene, 7-bromobenz[a]anthracene, and 6,12-dibromochrysene, were measured using the Knudsen effusion method over the temperature range of 301 to 464 K. Enthalpies and entropies of sublimation of these compounds were determined via application of the Clausius-Clapeyron equation. The data were also compared with earlier published literature values to study the influence of halogen substitution on vapor pressure of PACs. As expected, the halogen substitution decreases vapor pressure compared with parent compounds but does not necessarily increase the enthalpy of sublimation. Furthermore, the decrease of vapor pressure also depends on the substitution position and the substituted halogen, and the di-substitution of chlorine and/or bromine decreases the vapor pressure compared with single halogen-substituted polycyclic aromatic hydrocarbons. In addition, the enthalpy of fusion and melting temperature of these 12 PACs were determined using differential scanning calorimetry and melting point analysis.

  9. Source apportionment of hydrocarbons measured in the Eagle Ford shale

    Science.gov (United States)

    Roest, G. S.; Schade, G. W.

    2016-12-01

    The rapid development of unconventional oil and gas in the US has led to hydrocarbon emissions that are yet to be accurately quantified. Emissions from the Eagle Ford Shale in southern Texas, one of the most productive shale plays in the U.S., have received little attention due to a sparse air quality monitoring network, thereby limiting studies of air quality within the region. We use hourly atmospheric hydrocarbon and meteorological data from three locations in the Eagle Ford Shale to assess their sources. Data are available from the Texas commission of environmental quality (TCEQ) air quality monitors in Floresville, a small town southeast of San Antonio and just north of the shale area; and Karnes city, a midsize rural city in the center of the shale. Our own measurements were carried out at a private ranch in rural Dimmit County in southern Texas from April to November of 2015. Air quality monitor data from the TCEQ were selected for the same time period. Non-negative matrix factorization in R (package NMF) was used to determine likely sources and their contributions above background. While the TCEQ monitor data consisted mostly of hydrocarbons, our own data include both CO, CO2, O3, and NOx. We find that rural Dimmit County hydrocarbons are dominated by oil and gas development sources, while central shale hydrocarbons at the TCEQ monitoring sites have a mix of sources including car traffic. However, oil and gas sources also dominate hydrocarbons at Floresville and Karnes City. Toxic benzene is nearly exclusively due to oil and gas development sources, including flaring, which NMF identifies as a major hydrocarbon source in Karnes City. Other major sources include emissions of light weight alkanes (C2-C5) from raw natural gas emissions and a larger set of alkanes (C2-C10) from oil sources, including liquid storage tanks.

  10. Vapor concentration monitor

    Science.gov (United States)

    Bayly, John G.; Booth, Ronald J.

    1977-01-01

    An apparatus for monitoring the concentration of a vapor, such as heavy water, having at least one narrow bandwidth in its absorption spectrum, in a sample gas such as air. The air is drawn into a chamber in which the vapor content is measured by means of its radiation absorption spectrum. High sensitivity is obtained by modulating the wavelength at a relatively high frequency without changing its optical path, while high stability against zero drift is obtained by the low frequency interchange of the sample gas to be monitored and of a reference sample. The variable HDO background due to natural humidity is automatically corrected.

  11. Online measurements of the emissions of intermediate-volatility and semi-volatile organic compounds from aircraft

    Directory of Open Access Journals (Sweden)

    E. S. Cross

    2013-08-01

    Full Text Available A detailed understanding of the climate and air quality impacts of aviation requires measurements of the emissions of intermediate-volatility and semi-volatile organic compounds (I/SVOCs from aircraft. Currently both the amount and chemical composition of aircraft I/SVOC emissions remain poorly characterized. Here we characterize I/SVOC emissions from aircraft, using a novel instrument for the online, quantitative measurement of the mass loading and composition of low-volatility organic vapors. Emissions from the NASA DC8 aircraft were sampled on the ground 143 m downwind of the engines and characterized as a function of engine power from idle (4% maximum rated thrust through 85% power. Results show that I/SVOC emissions are highest during engine idle operating conditions, with decreasing but non-zero I/SVOC emissions at higher engine powers. Comparison of I/SVOC emissions with total hydrocarbon (THC measurements, VOC measurements, and an established emissions profile indicates that I/SVOCs comprise 10–20% of the total organic gas-phase emissions at idle, and an increasing fraction of the total gas-phase organic emissions at higher powers. Positive matrix factorization of online mass spectra is used to identify three distinct types of I/SVOC emissions: aliphatic, aromatic and oxygenated. The volatility and chemical composition of the emissions suggest that unburned fuel is the dominant source of I/SVOCs at idle, while pyrolysis products make up an increasing fraction of the I/SVOCs at higher powers. Oxygenated I/SVOC emissions were detected at lower engine powers (≤30% and may be linked to cracked, partially oxidized or unburned fuel components.

  12. Online measurements of the emissions of intermediate-volatility and semi-volatile organic compounds from aircraft

    Directory of Open Access Journals (Sweden)

    E. S. Cross

    2013-03-01

    Full Text Available A detailed understanding of the climate and air quality impacts of aviation requires detailed measurements of the emissions of intermediate-volatility and semi-volatile organic compounds (I/SVOCs from aircraft. Currently both the amount and chemical composition of aircraft I/SVOC emissions remain poorly characterized. Here we characterize I/SVOC emissions from aircraft, using a novel instrument for the online, quantitative measurement of the mass loading and composition of low-volatility organic vapors. Emissions from the NASA DC8 aircraft were sampled on the ground, 143 m downwind of the engines and characterized as a function of engine power from ground idle (~4% maximum rated thrust through 85% power. Results show that I/SVOC emissions are highest during engine-idle operating conditions, with decreasing but non-zero I/SVOC emissions at higher engine powers. Comparison of I/SVOC emissions with total hydrocarbon (THC measurements, VOC measurements, and an established emissions profile indicates that I/SVOCs comprise 10–20% of the total organic gas phase emissions at idle, and an increasing fraction of the total gas phase organic emissions at higher powers. Positive matrix factorization of online mass spectra is used to identify three distinct types of I/SVOC emissions: aliphatic, aromatic and oxygenated. The volatility and chemical composition of the emissions suggest that unburned fuel is the dominant source of I/SVOCs at idle, while pyrolysis products make up an increasing fraction of the I/SVOCs at higher powers. Oxygenated I/SVOC emissions were detected at lower engine powers (≤30% and may be linked to cracked, partially oxidized or unburned fuel components.

  13. Quantitative Hydrocarbon Surface Analysis

    Science.gov (United States)

    Douglas, Vonnie M.

    2000-01-01

    The elimination of ozone depleting substances, such as carbon tetrachloride, has resulted in the use of new analytical techniques for cleanliness verification and contamination sampling. The last remaining application at Rocketdyne which required a replacement technique was the quantitative analysis of hydrocarbons by infrared spectrometry. This application, which previously utilized carbon tetrachloride, was successfully modified using the SOC-400, a compact portable FTIR manufactured by Surface Optics Corporation. This instrument can quantitatively measure and identify hydrocarbons from solvent flush of hardware as well as directly analyze the surface of metallic components without the use of ozone depleting chemicals. Several sampling accessories are utilized to perform analysis for various applications.

  14. Miscellaneous hydrocarbon solvents.

    Science.gov (United States)

    Bebarta, Vikhyat; DeWitt, Christopher

    2004-08-01

    The solvents discussed in this article are common solvents not categorized as halogenated, aromatic, or botanical. The solvents discussed are categorized into two groups: hydrocarbon mixtures and single agents. The hydrocarbon mixtures discussed are Stoddard solvent, naphtha, and kerosene. The remaining solvents described are n-hexane, methyl n-butyl ketone, dimethylformamide, dimethyl sulfoxide, and butyl mercaptans. Effects common to this group of agents and their unique effects are characterized. Treatment of exposures and toxic effects of these solvents is described, and physiochemical properties and occupational exposure levels are listed.

  15. Chemical composition of hydrocarbons from semicoking tars of lignites from the near-Moscow fields

    Energy Technology Data Exchange (ETDEWEB)

    Platonov, V.V.; Proskuryakov, V.A.; Antonio, T.Z.; Platonova, M.V. [Lev Tolstoi Pedagogical University, Tula (Russian Federation)

    1998-09-01

    The chemical composition of hydrocarbons from the semicoking tar of lignites was studied by elemental, functional, emission spectrum, and structural-group analyses, cryoscopy, IR, UV and {sup 1}H and {sup 13}C NMR spectroscopy, capillary gas chromatography, and gas chromatography-mass spectrometry. A scheme was developed for adsorption liquid chromatography of the hydrocarbons.

  16. Limitations of microbial hydrocarbon degradation at the Amon mud volcano (Nile deep-sea fan)

    NARCIS (Netherlands)

    Felden, J.; Lichtschlag, A.; Wenzhöfer, F.; de Beer, D.; Feseker, T.; Pop Ristova, P.; de Lange, G.; Boetius, A.

    2013-01-01

    The Amon mud volcano (MV), located at 1250m water depth on the Nile deep-sea fan, is known for its active emission of methane and non-methane hydrocarbons into the hydrosphere. Previous investigations showed a low efficiency of hydrocarbon-degrading anaerobic microbial communities inhabiting the Amo

  17. Passive Vaporizing Heat Sink

    Science.gov (United States)

    Knowles, TImothy R.; Ashford, Victor A.; Carpenter, Michael G.; Bier, Thomas M.

    2011-01-01

    A passive vaporizing heat sink has been developed as a relatively lightweight, compact alternative to related prior heat sinks based, variously, on evaporation of sprayed liquids or on sublimation of solids. This heat sink is designed for short-term dissipation of a large amount of heat and was originally intended for use in regulating the temperature of spacecraft equipment during launch or re-entry. It could also be useful in a terrestrial setting in which there is a requirement for a lightweight, compact means of short-term cooling. This heat sink includes a hermetic package closed with a pressure-relief valve and containing an expendable and rechargeable coolant liquid (e.g., water) and a conductive carbon-fiber wick. The vapor of the liquid escapes when the temperature exceeds the boiling point corresponding to the vapor pressure determined by the setting of the pressure-relief valve. The great advantage of this heat sink over a melting-paraffin or similar phase-change heat sink of equal capacity is that by virtue of the =10x greater latent heat of vaporization, a coolant-liquid volume equal to =1/10 of the paraffin volume can suffice.

  18. Distillation-Based Droplet Modeling of Non-Ideal Oxygenated Gasoline Blends: Investigating the Role of Droplet Evaporation on PM Emissions

    Energy Technology Data Exchange (ETDEWEB)

    Burke, Stephen C.; Ratcliff, Matthew; McCormick, Robert; Rhoads, Robert; Windom, Bret

    2017-03-28

    In some studies, a relationship has been observed between increasing ethanol content in gasoline and increased particulate matter (PM) emissions from vehicles equipped with spark ignition engines. The fundamental cause of the PM increase seen for moderate ethanol concentrations is not well understood. Ethanol features a greater heat of vaporization (HOV) than gasoline and also influences vaporization by altering the liquid and vapor composition throughout the distillation process. A droplet vaporization model was developed to explore ethanol's effect on the evaporation of aromatic compounds known to be PM precursors. The evolving droplet composition is modeled as a distillation process, with non-ideal interactions between oxygenates and hydrocarbons accounted for using UNIFAC group contribution theory. Predicted composition and distillation curves were validated by experiments. Detailed hydrocarbon analysis was applied to fuel samples and to distillate fractions, and used as input for the initial droplet composition. With composition calculated throughout the distillation, the changing HOV and other physical properties can be found using reference data. The droplet can thus be modeled in terms of energy transfer, which in turn provides the transient mass transfer, droplet temperature, and droplet diameter. Model predictions suggest that non-ideal vapor-liquid equilibrium along with an increase in HOV can alter the droplet composition evolution. Results predict that the presence of ethanol causes enrichment of the higher boiling fractions (T90+) in the aromatic components as well as lengthens the droplet lifetime. A simulation of the evaporation process in a transient environment as experienced within an engine cylinder predicts a decrease in mixing time of the heaviest fractions of the fuel prior to spark initiation, possibly explaining observations linking ethanol to PM.

  19. Apparatus and methods for hydrocarbon extraction

    Science.gov (United States)

    Bohnert, George W.; Verhulst, Galen G.

    2016-04-26

    Systems and methods for hydrocarbon extraction from hydrocarbon-containing material. Such systems and methods relate to extracting hydrocarbon from hydrocarbon-containing material employing a non-aqueous extractant. Additionally, such systems and methods relate to recovering and reusing non-aqueous extractant employed for extracting hydrocarbon from hydrocarbon-containing material.

  20. Simulation of the high-pressure phase equilibria of hydrocarbon-water/brine systems

    DEFF Research Database (Denmark)

    Zuo, You-Xiang; Stenby, Erling Halfdan; Guo, Tian-Min

    1996-01-01

    The major objectives of this work are: (1) extend the modified Patel-Teja (MPT) equation of state proposed for aqueous electrolyte systems (Zuo and Guo, 1991) to describe the liquid-liquid and vapor-liquid-liquid equilibria of hydrocarbon-water/brine systems through introducing an unconventional ...

  1. Supercooled liquid vapour pressures and related thermodynamic properties of polycyclic aromatic hydrocarbons determined by gas chromatography

    NARCIS (Netherlands)

    Haftka, J.J.H.; Parsons, J.R.; Govers, H.A.J.

    2006-01-01

    A gas chromatographic method using Kovats retention indices has been applied to determine the liquid vapour pressure (P-i), enthalpy of vaporization (Delta H-i) and difference in heat capacity between gas and liquid phase (Delta C-i) for a group of polycyclic aromatic hydrocarbons (PAHs). This group

  2. A review of catalytic aqueous-phase reforming of oxygenated hydrocarbons derived from biorefinery water fractions

    NARCIS (Netherlands)

    Coronado, I.; Stekrova, M.; Reinikainen, M.; Simell, P.; Lefferts, Leonardus; Lehtonen, J.

    2016-01-01

    Aqueous-phase reforming (APR) of oxygenated hydrocarbons is a process for the production of hydrogen and light alkanes. The reactants of APR remain in liquid phase during the reaction avoiding an energetically demanding vaporization-step compared to processes such as steam reforming (SR).

  3. Mantle hydrocarbons: abiotic or biotic?

    Science.gov (United States)

    Sugisaki, R; Mimura, K

    1994-06-01

    Analyses of 227 rocks from fifty localities throughout the world showed that mantle derived rocks such as tectonized peridotites in ophiolite sequences (tectonites) arid peridotite xenoliths in alkali basalts contain heavier hydrocarbons (n-alkanes), whereas igneous rocks produced by magmas such as gabbro arid granite lack them. The occurrence of hydrocarbons indicates that they were not derived either from laboratory contamination or from held contamination; these compounds found in the mantle-derived rocks are called here "mantle hydrocarbons." The existence of hydrocarbons correlates with petrogenesis. For example, peridotite cumulates produced by magmatic differentiation lack hydrocarbons whereas peridotite xenoliths derived from the mantle contain them. Gas chromatographic-mass spectrometric records of the mantle hydrocarbons resemble those of aliphatics in meteorites and in petroleum. Features of the hydrocarbons are that (a) the mantle hydrocarbons reside mainly along grain boundaries and in fluid inclusions of minerals; (b) heavier isoprenoids such as pristane and phytane are present; and (c) delta 13C of the mantle hydrocarbons is uniform (about -27%). Possible origins for the mantle hydrocarbons are as follows. (1) They were in organically synthesized by Fischer-Tropsch type reaction in the mantle. (2) They were delivered by meteorites and comets to the early Earth. (3) They were recycled by subduction. The mantle hydrocarbons in the cases of (1) and (2) are abiogenic and those in (3) are mainly biogenic. It appears that hydrocarbons may survive high pressures and temperatures in the mantle, but they are decomposed into lighter hydrocarbon gases such as CH4 at lower pressures when magmas intrude into the crust; consequently, peridotite cumulates do not contain heavier hydrocarbons but possess hydrocarbon gases up to C4H10.

  4. CO and PAH emissions from engines operating on producer gas

    DEFF Research Database (Denmark)

    Ahrenfeldt, Jesper

    2005-01-01

    from the start been that a high CO emission is a measure for incomplete combustion of hydrocarbons and thus an indicator for the presents of organic micro emissions such as polynuclear aromatic hydrocarbons (PAH). Measurements from two operating gasification plants show that there is no correlation...... between the high CO emissions and PAH emissions from engines operating on producer gas. The measured PAH emissions were more than 20 times lower than the recommended emission limit for gas engines. Since unburned CO and UHC are similar in origin the reasonable regulated limit for CO emissions from engines...

  5. Bacterial sources for phenylalkane hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Ellis, L.; Winans, R.E. [Argonne National Lab., IL (United States); Langworthy, T. [Univ. of South Dakota, Vermillion, SD (United States)

    1996-10-01

    The presence of phenylalkane hydrocarbons in geochemical samples has been the source of much controversy. Although an anthropogenic input from detergent sources always appears likely, the distribution of phenylalkane hydrocarbons in some cases far exceeding that attributed to detergent input has led to a reappraisal of this view. Indeed, recent work involving analysis of the lipid hydrocarbon extracts from extant Thermoplasma bacteria has revealed the presence of phenylalkane hydrocarbons. The presence of phenylalkane hydrocarbons in sedimentary organic matter may therefore represent potential biological markers for thermophilic bacteria.

  6. Methane Decomposition and C2 Hydrocarbon Formation under the Condition of DC Discharge Plasma

    Institute of Scientific and Technical Information of China (English)

    Jianxun He; Miao Hu; Zhiguo Lu

    2004-01-01

    The infrared emission spectra of methane, H, CH and C2 hydrocarbons in natural gas were measured. The processes of methane decomposition and formation of C2 hydrocarbons were studied. The experiment shows that methane decomposition can be divided into three periods as the reaction proceeds.In the first period, a large number of free radicals were formed. While in the last period, the formation of C2 hydrocarbons and the decrease of free radicals were observed. The time and conditions of methane decomposition and formation of C2 hydrocarbons are different.

  7. Water vapor: An extraordinary terahertz wave source under optical excitation

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, Keith [Massachusetts Institute of Technology, PO Box 380792, Cambridge, MA 02238-0792 (United States); HydroElectron Ventures Inc., 1303 Greene Avenue Suite 102, Westmount, QC, H3Z 2A7 (Canada)], E-mail: kjohnson@mit.edu; Price-Gallagher, Matthew [HydroElectron Ventures Inc., 1303 Greene Avenue Suite 102, Westmount, QC, H3Z 2A7 (Canada); Mamer, Orval; Lesimple, Alain [Mass Spectroscopy Unit, 740 Dr. Penfield, Suite 5300, McGill University, Montreal, QC, H3A 1A4 (Canada); Fletcher, Clark [HydroElectron Ventures Inc., 1303 Greene Avenue Suite 102, Westmount, QC, H3Z 2A7 (Canada); Chen Yunqing; Lu Xiaofei; Yamaguchi, Masashi; Zhang, X.-C. [W.M. Keck Laboratory for Terahertz Science, Center for Terahertz Research, Rensselaer Polytechnic Institute, Troy, NY 12180 (United States)

    2008-09-15

    In modern terahertz (THz) sensing and imaging spectroscopy, water is considered a nemesis to be avoided due to strong absorption in the THz frequency range. Here we report the first experimental demonstration and theoretical implications of using femtosecond laser pulses to generate intense broadband THz emission from water vapor. When we focused an intense laser pulse in water vapor contained in a gas cell or injected from a gas jet nozzle, an extraordinarily strong THz field from optically excited water vapor is observed. Water vapor has more than 50% greater THz generation efficiency than dry nitrogen. It had previously been assumed that the nonlinear generation of THz waves in this manner primarily involves a free-electron plasma, but we show that the molecular structure plays an essential role in the process. In particular, we found that THz wave generation from H{sub 2}O vapor is significantly stronger than that from D{sub 2}O vapor. Vibronic activities of water cluster ions, occurring naturally in water vapor, may possibly contribute to the observed isotope effect along with rovibrational contributions from the predominant monomers.

  8. Influence of absorption by environmental water vapor on radiation transfer in wildland fires

    Science.gov (United States)

    D. Frankman; B. W. Webb; B. W. Butler

    2008-01-01

    The attenuation of radiation transfer from wildland flames to fuel by environmental water vapor is investigated. Emission is tracked from points on an idealized flame to locations along the fuel bed while accounting for absorption by environmental water vapor in the intervening medium. The Spectral Line Weighted-sum-of-gray-gases approach was employed for treating the...

  9. 76 FR 61062 - Approval and Promulgation of Implementation Plans; Arizona; Update to Stage II Gasoline Vapor...

    Science.gov (United States)

    2011-10-03

    ...; Update to Stage II Gasoline Vapor Recovery Program; Change in the Definition of ``Gasoline'' To Exclude... emissions from the transfer of gasoline from storage tanks to motor vehicle fuel tanks at gasoline dispensing sites, i.e., stage II vapor recovery. The revisions would also amend the definition of...

  10. Trace element emissions when firing pulverized coal in a pilot-scale combustion facility

    Energy Technology Data Exchange (ETDEWEB)

    Miller, S.F.; Wincek, R.T.; Miller, B.G.; Scaroni, A.W.

    1998-07-01

    Strategies are being developed at Penn State to produce ultralow emissions when firing coal-based fuels, i.e., micronized coal and coal-water slurry fuel (CWSF), in industrial boilers. The work is being conducted on the bench, pilot, and demonstration scale, and the emissions being addressed are SO{sub 2}, NO{sub x}, fine particulate matter (PM{sub 10} and PM{sub 2.5}), and air toxics (trace elements and volatile organic compounds). Technical issues related to trace element emissions that are to be addressed include: (1) the effectiveness of coal cleaning; (2) the effect of fuel form (CWSF and pulverized coal); (3) partitioning between the solid and vapor phases; (4) the effect of boiler size; (5) penetration through particulate control devices; (6) the effect of sootblowing; and (7) mercury speciation. This paper discusses the results of preliminary work to determine trace element emissions when firing a raw and cleaned pulverized coal in a pilot-scale combustor. A companion paper, which follows in the proceedings, gives the results of polynuclear aromatic hydrocarbon (PAH) emissions testing in the pilot-scale combustor and in a small industrial boiler. Results from fine particulate testing is found elsewhere in the proceedings.

  11. Microbial degradation of petroleum hydrocarbons.

    Science.gov (United States)

    Varjani, Sunita J

    2017-01-01

    Petroleum hydrocarbon pollutants are recalcitrant compounds and are classified as priority pollutants. Cleaning up of these pollutants from environment is a real world problem. Bioremediation has become a major method employed in restoration of petroleum hydrocarbon polluted environments that makes use of natural microbial biodegradation activity. Petroleum hydrocarbons utilizing microorganisms are ubiquitously distributed in environment. They naturally biodegrade pollutants and thereby remove them from the environment. Removal of petroleum hydrocarbon pollutants from environment by applying oleophilic microorganisms (individual isolate/consortium of microorganisms) is ecofriendly and economic. Microbial biodegradation of petroleum hydrocarbon pollutants employs the enzyme catalytic activities of microorganisms to enhance the rate of pollutants degradation. This article provides an overview about bioremediation for petroleum hydrocarbon pollutants. It also includes explanation about hydrocarbon metabolism in microorganisms with a special focus on new insights obtained during past couple of years. Copyright © 2016 Elsevier Ltd. All rights reserved.

  12. Superconductivity in aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Kubozono, Yoshihiro, E-mail: kubozono@cc.okayama-u.ac.jp [Research Laboratory for Surface Science, Okayama University, Okayama 700-8530 (Japan); Research Center of New Functional Materials for Energy Production, Storage and Transport, Okayama University, Okayama 700-8530 (Japan); Japan Science and Technology Agency, ACT-C, Kawaguchi 332-0012 (Japan); Goto, Hidenori; Jabuchi, Taihei [Research Laboratory for Surface Science, Okayama University, Okayama 700-8530 (Japan); Yokoya, Takayoshi [Research Laboratory for Surface Science, Okayama University, Okayama 700-8530 (Japan); Research Center of New Functional Materials for Energy Production, Storage and Transport, Okayama University, Okayama 700-8530 (Japan); Kambe, Takashi [Department of Physics, Okayama University, Okayama 700-8530 (Japan); Sakai, Yusuke; Izumi, Masanari; Zheng, Lu; Hamao, Shino; Nguyen, Huyen L.T. [Research Laboratory for Surface Science, Okayama University, Okayama 700-8530 (Japan); Sakata, Masafumi; Kagayama, Tomoko; Shimizu, Katsuya [Center of Science and Technology under Extreme Conditions, Osaka University, Osaka 560-8531 (Japan)

    2015-07-15

    Highlights: • Aromatic superconductor is one of core research subjects in superconductivity. Superconductivity is observed in certain metal-doped aromatic hydrocarbons. Some serious problems to be solved exist for future advancement of the research. This article shows the present status of aromatic superconductors. - Abstract: ‘Aromatic hydrocarbon’ implies an organic molecule that satisfies the (4n + 2) π-electron rule and consists of benzene rings. Doping solid aromatic hydrocarbons with metals provides the superconductivity. The first discovery of such superconductivity was made for K-doped picene (K{sub x}picene, five benzene rings). Its superconducting transition temperatures (T{sub c}’s) were 7 and 18 K. Recently, we found a new superconducting K{sub x}picene phase with a T{sub c} as high as 14 K, so we now know that K{sub x}picene possesses multiple superconducting phases. Besides K{sub x}picene, we discovered new superconductors such as Rb{sub x}picene and Ca{sub x}picene. A most serious problem is that the shielding fraction is ⩽15% for K{sub x}picene and Rb{sub x}picene, and it is often ∼1% for other superconductors. Such low shielding fractions have made it difficult to determine the crystal structures of superconducting phases. Nevertheless, many research groups have expended a great deal of effort to make high quality hydrocarbon superconductors in the five years since the discovery of hydrocarbon superconductivity. At the present stage, superconductivity is observed in certain metal-doped aromatic hydrocarbons (picene, phenanthrene and dibenzopentacene), but the shielding fraction remains stubbornly low. The highest priority research area is to prepare aromatic superconductors with a high superconducting volume-fraction. Despite these difficulties, aromatic superconductivity is still a core research target and presents interesting and potentially breakthrough challenges, such as the positive pressure dependence of T{sub c} that is clearly

  13. Native Fluorescence Detection Methods and Detectors for Naphthalene and/or Other Volatile Organic Compound Vapors

    Science.gov (United States)

    Hug, William F. (Inventor); Bhartia, Rohit (Inventor); Reid, Ray D. (Inventor); Lane, Arthur L. (Inventor)

    2014-01-01

    Naphthalene, benzene, toluene, xylene, and other volatile organic compounds have been identified as serious health hazards. This is especially true for personnel working with JP8 jet fuel and other fuels containing naphthalene as well as other hazardous volatile organic compounds (VOCs). Embodiments of the invention are directed to methods and apparatus for near-real-time in-situ detection and accumulated dose measurement of exposure to naphthalene vapor and other hazardous gaseous VOCs. The methods and apparatus employ excitation of fluorophors native or endogenous to compounds of interest using light sources emitting in the ultraviolet below 300 nm and measurement of native fluorescence emissions in distinct wavebands above the excitation wavelength. The apparatus of some embodiments are cell-phone-sized sensor/dosimeter "badges" to be worn by personnel potentially exposed to naphthalene or other hazardous VOCs. The badge sensor of some embodiments provides both real time detection and data logging of exposure to naphthalene or other VOCs of interest from which both instantaneous and accumulated dose can be determined. The badges employ a new native fluorescence based detection method to identify and differentiate VOCs. The particular focus of some embodiments are the detection and identification of naphthalene while other embodiments are directed to detection and identification of other VOCs like aromatic hydrocarbons such as benzene, toluene, and xylene.

  14. VAPOR PRESSURES AND HEATS OF VAPORIZATION OF PRIMARY COAL TARS

    Energy Technology Data Exchange (ETDEWEB)

    Eric M. Suuberg; Vahur Oja

    1997-07-01

    This project had as its main focus the determination of vapor pressures of coal pyrolysis tars. It involved performing measurements of these vapor pressures and from them, developing vapor pressure correlations suitable for use in advanced pyrolysis models (those models which explicitly account for mass transport limitations). This report is divided into five main chapters. Each chapter is a relatively stand-alone section. Chapter A reviews the general nature of coal tars and gives a summary of existing vapor pressure correlations for coal tars and model compounds. Chapter B summarizes the main experimental approaches for coal tar preparation and characterization which have been used throughout the project. Chapter C is concerned with the selection of the model compounds for coal pyrolysis tars and reviews the data available to us on the vapor pressures of high boiling point aromatic compounds. This chapter also deals with the question of identifying factors that govern the vapor pressures of coal tar model materials and their mixtures. Chapter D covers the vapor pressures and heats of vaporization of primary cellulose tars. Chapter E discusses the results of the main focus of this study. In summary, this work provides improved understanding of the volatility of coal and cellulose pyrolysis tars. It has resulted in new experimentally verified vapor pressure correlations for use in pyrolysis models. Further research on this topic should aim at developing general vapor pressure correlations for all coal tars, based on their molecular weight together with certain specific chemical characteristics i.e. hydroxyl group content.

  15. Membrane separation of hydrocarbons

    Science.gov (United States)

    Chang, Y. Alice; Kulkarni, Sudhir S.; Funk, Edward W.

    1986-01-01

    Mixtures of heavy oils and light hydrocarbons may be separated by passing the mixture through a polymeric membrane. The membrane which is utilized to effect the separation comprises a polymer which is capable of maintaining its integrity in the presence of hydrocarbon compounds and which has been modified by being subjected to the action of a sulfonating agent. Sulfonating agents which may be employed will include fuming sulfuric acid, chlorosulfonic acid, sulfur trioxide, etc., the surface or bulk modified polymer will contain a degree of sulfonation ranging from about 15 to about 50%. The separation process is effected at temperatures ranging from about ambient to about 100.degree. C. and pressures ranging from about 50 to about 1000 psig.

  16. Direct hydrocarbon fuel cells

    Science.gov (United States)

    Barnett, Scott A.; Lai, Tammy; Liu, Jiang

    2010-05-04

    The direct electrochemical oxidation of hydrocarbons in solid oxide fuel cells, to generate greater power densities at lower temperatures without carbon deposition. The performance obtained is comparable to that of fuel cells used for hydrogen, and is achieved by using novel anode composites at low operating temperatures. Such solid oxide fuel cells, regardless of fuel source or operation, can be configured advantageously using the structural geometries of this invention.

  17. THERMOCHEMISTRY OF HYDROCARBON RADICALS

    Energy Technology Data Exchange (ETDEWEB)

    Kent M. Ervin, Principal Investigator

    2004-08-17

    Gas phase negative ion chemistry methods are employed to determine enthalpies of formation of hydrocarbon radicals that are important in combustion processes and to investigate the dynamics of ion-molecule reactions. Using guided ion beam tandem mass spectrometry, we measure collisional threshold energies of endoergic proton transfer and hydrogen atom transfer reactions of hydrocarbon molecules with negative reagent ions. The measured reaction threshold energies for proton transfer yield the relative gas phase acidities. In an alternative methodology, competitive collision-induced dissociation of proton-bound ion-molecule complexes provides accurate gas phase acidities relative to a reference acid. Combined with the electron affinity of the R {center_dot} radical, the gas phase acidity yields the RH bond dissociation energy of the corresponding neutral molecule, or equivalently the enthalpy of formation of the R{center_dot} organic radical, using equation: D(R-H) = {Delta}{sub acid}H(RH) + EA(R) - IE(H). The threshold energy for hydrogen abstraction from a hydrocarbon molecule yields its hydrogen atom affinity relative to the reagent anion, providing the RH bond dissociation energy directly. Electronic structure calculations are used to evaluate the possibility of potential energy barriers or dynamical constrictions along the reaction path, and as input for RRKM and phase space theory calculations. In newer experiments, we have measured the product velocity distributions to obtain additional information on the energetics and dynamics of the reactions.

  18. Variable emissivity laser thermal control system

    Science.gov (United States)

    Milner, Joseph R.

    1994-01-01

    A laser thermal control system for a metal vapor laser maintains the wall mperature of the laser at a desired level by changing the effective emissivity of the water cooling jacket. This capability increases the overall efficiency of the laser.

  19. Atmospheric polycyclic aromatic hydrocarbons in north China: a winter-time study.

    Science.gov (United States)

    Liu, Shuzhen; Tao, Shu; Liu, Wenxin; Liu, Yanan; Dou, Han; Zhao, Jingyu; Wang, Luguang; Wang, Jingfei; Tian, Zaifeng; Gao, Yuan

    2007-12-15

    The contamination and outflow of atmospheric polycyclic aromatic hydrocarbons (PAHs) in the Chinese Northern Plain, a region with a total area of 300 000 km2 and a high PAH emission density, were investigated. Polyurethane foam (PUF) and PM10 samples were collected at 46 sites located in urban, rural (towns or villages), and control (remote mountain) areas in the winter from November 2005 to February 2006. The observed concentrations of atmospheric PAHs were generally higher than those reported for developed countries and southern Chinese cities. It was found that there was no significant difference in air PAH concentrations between the urban and the rural areas (514 +/- 563 ng/m3 and 610 +/- 645 ng/ m3, respectively), while the PAH concentrations at the control sites (57.1 +/- 12.6 ng/m3) were 1 order of magnitude lower than those at the other sites. The primary reason for the similarity in PAH concentrations between urban and rural areas was the fact that the predominant sources of biomass and domestic coal combustion were widely spread over the study area. The partition constants (K(PM10)) of PAHs were significantly correlated to the corresponding values of subcooled liquid-vapor pressure (pL0). However, the regression slopes of log K(PM10) versus log pL0 were much steeper than -1, indicating adsorption dominated over absorption. Three distinct patterns of outflow from the study area were identified by forward trajectory and cluster analysis.

  20. Particulate hydroxy-PAH emissions from a residential wood log stove using different fuels and burning conditions

    Science.gov (United States)

    Avagyan, Rozanna; Nyström, Robin; Lindgren, Robert; Boman, Christoffer; Westerholm, Roger

    2016-09-01

    Hydroxylated polycyclic aromatic hydrocarbons are oxidation products of polycyclic aromatic hydrocarbons, but have not been studied as extensively as polycyclic aromatic hydrocarbons. Several studies have however shown that hydroxylated polycyclic aromatic hydrocarbons have toxic and carcinogenic properties. They have been detected in air samples in semi urban areas and combustion is assumed to be the primary source of those compounds. To better understand the formation and occurrence of particulate hydroxylated polycyclic aromatic hydrocarbons from residential wood log stove combustion, 9 hydroxylated polycyclic aromatic hydrocarbons and 2 hydroxy biphenyls were quantified in particles generated from four different types of wood logs (birch, spruce, pine, aspen) and two different combustion conditions (nominal and high burn rate). A previously developed method utilizing liquid chromatography - photo ionization tandem mass spectrometry and pressurized liquid extraction was used. Polycyclic aromatic hydrocarbons were analyzed along with hydroxylated polycyclic aromatic hydrocarbons. The hydroxylated polycyclic aromatic hydrocarbon emissions varied significantly across different wood types and burning conditions; the highest emissions for nominal burn rate were from spruce and for high burn rate from pine burning. Emissions from nominal burn rate corresponded on average to 15% of the emissions from high burn rate, with average emissions of 218 μg/MJfuel and 32.5 μg/MJfuel for high burn rate and nominal burn rate, respectively. Emissions of the measured hydroxylated polycyclic aromatic hydrocarbons corresponded on average to 28% of polycyclic aromatic hydrocarbons emissions. This study shows that wood combustion is a large emission source of hydroxylated polycyclic aromatic hydrocarbons and that not only combustion conditions, but also wood type influences the emissions of hydroxylated polycyclic aromatic hydrocarbons and polycyclic aromatic hydrocarbons. There are

  1. Experimental Study on the Characteristics Polycyclic Aromatic Hydrocarbon Emissions of Diesel Engine Burnt by Different Fuels%不同燃料柴油机多环芳烃排放特征的试验研究

    Institute of Scientific and Technical Information of China (English)

    王忠; 安玉光; 许广举; 王小哲

    2011-01-01

    The polycyclic aromatic hydrocarbons(PAHs) were measured by glass fiber filter and XAD-2 collector,ultrasonic extraction,soxhlet extraction and GC-MS analysis equipment.The exhaust emission of the DI single cylinder diesel engine fueled with pure diesel,biodiesel and biodiesel blends of 50%(B50) were measured.The results indicate that the particle-phase PAHs emissions of diesel engine decrease with the increasing of load.The gas-phase PAHs emissions of diesel engine decrease with the increasing of load in the beginning and it turns to going up with further increasing of load.The particle-phase and gas-phase PAHs emissions of biodiesel decrease and mean concentration are lower than that of diesel.The total PAHs emission concentration of biodisesl is 41.1-70.1μg/m^3.Total PAHs mean concentration emissions of biodiesel is decreased 33.3% than that of diesel.The mass proportion of three-ring PAHs emissions of those 3 kinds tested fuels is about 44% in the total PAHs.Biodiesel can increase the proportion of three-ring PAHs.Toxic equivalence of PAHs emissions of biodiesel are greatly lower than that of diesel.It is less harmful to human than diesel fuel.%在一台直喷式柴油机上,采用玻璃纤维滤纸及XAD-2吸附管采集、超声和索氏提取、气质联用分析等技术,测量了燃用柴油、生物柴油及其调合油B50排气中的多环芳烃类污染物(PAHs).研究表明,柴油机颗粒相PAHs排放随着负荷的增大呈现降低的趋势,气相PAHs排放随着负荷呈现先降低后升高的趋势.与柴油相比,生物柴油的颗粒相和气相PAHs排放有所降低,其平均排放浓度也均低于柴油.生物柴油排气中总PAHs排放浓度为41.1~70.1μg/m^3,总PAHs的平均排放浓度与柴油相比下降了33.3%.3种不同燃料的三环P

  2. Deuterated polycyclic aromatic hydrocarbons: Revisited

    CERN Document Server

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

    2016-01-01

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

  3. Numerical model investigation for potential methane explosion and benzene vapor intrusion associated with high-ethanol blend releases.

    Science.gov (United States)

    Ma, Jie; Luo, Hong; Devaull, George E; Rixey, William G; Alvarez, Pedro J J

    2014-01-01

    Ethanol-blended fuel releases usually stimulate methanogenesis in the subsurface, which could pose an explosion risk if methane accumulates in a confined space above the ground where ignitable conditions exist. Ethanol-derived methane may also increase the vapor intrusion potential of toxic fuel hydrocarbons by stimulating the depletion of oxygen by methanotrophs, and thus inhibiting aerobic biodegradation of hydrocarbon vapors. To assess these processes, a three-dimensional numerical vapor intrusion model was used to simulate the degradation, migration, and intrusion pathway of methane and benzene under different site conditions. Simulations show that methane is unlikely to build up to pose an explosion hazard (5% v/v) if diffusion is the only mass transport mechanism through the deeper vadose zone. However, if methanogenic activity near the source zone is sufficiently high to cause advective gas transport, then the methane indoor concentration may exceed the flammable threshold under simulated conditions. During subsurface migration, methane biodegradation could consume soil oxygen that would otherwise be available to support hydrocarbon degradation, and increase the vapor intrusion potential for benzene. Vapor intrusion would also be exacerbated if methanogenic activity results in sufficiently high pressure to cause advective gas transport in the unsaturated zone. Overall, our simulations show that current approaches to manage the vapor intrusion risk for conventional fuel released might need to be modified when dealing with some high ethanol blend fuel (i.e., E20 up to E95) releases.

  4. Air exchange rates and alternative vapor entry pathways to inform vapor intrusion exposure risk assessments.

    Science.gov (United States)

    Reichman, Rivka; Roghani, Mohammadyousef; Willett, Evan J; Shirazi, Elham; Pennell, Kelly G

    2016-11-12

    Vapor intrusion (VI) is a term used to describe indoor air (IA) contamination that occurs due to the migration of chemical vapors in the soil and groundwater. The overall vapor transport process depends on several factors such as contaminant source characteristics, subsurface conditions, building characteristics, and general site conditions. However, the classic VI conceptual model does not adequately account for the physics of airflow around and inside a building and does not account for chemical emissions from alternative "preferential" pathways (e.g. sewers and other utility connections) into IA spaces. This mini-review provides information about recent research related to building air exchange rates (AERs) and alternative pathways to improve the accuracy of VI exposure risk assessment practices. First, results from a recently published AER study for residential homes across the United States (US) are presented and compared to AERs recommended by the US Environmental Protection Agency (USEPA). The comparison shows considerable differences in AERs when season, location, building age, and other factors are considered. These differences could directly impact VI assessments by influencing IA concentration measurements. Second, a conceptual model for sewer gas entry into buildings is presented and a summary of published field studies is reported. The results of the field studies suggest that alternative pathways for vapors to enter indoor spaces warrant consideration. Ultimately, the information presented in this mini-review can be incorporated into a multiple-lines-of-evidence approach for assessing site-specific VI exposure risks.

  5. LNG pool fire spectral data and calculation of emissive power.

    Science.gov (United States)

    Raj, Phani K

    2007-04-11

    Spectral description of thermal emission from fires provides a fundamental basis on which the fire thermal radiation hazard assessment models can be developed. Several field experiments were conducted during the 1970s and 1980s to measure the thermal radiation field surrounding LNG fires. Most of these tests involved the measurement of fire thermal radiation to objects outside the fire envelope using either narrow-angle or wide-angle radiometers. Extrapolating the wide-angle radiometer data without understanding the nature of fire emission is prone to errors. Spectral emissions from LNG fires have been recorded in four test series conducted with LNG fires on different substrates and of different diameters. These include the AGA test series of LNG fires on land of diameters 1.8 and 6m, 35 m diameter fire on an insulated concrete dike in the Montoir tests conducted by Gaz de France, a 1976 test with 13 m diameter and the 1980 tests with 10 m diameter LNG fire on water carried out at China Lake, CA. The spectral data from the Montoir test series have not been published in technical journals; only recently has some data from this series have become available. This paper presents the details of the LNG fire spectral data from, primarily, the China Lake test series, their analysis and results. Available data from other test series are also discussed. China Lake data indicate that the thermal radiation emission from 13 m diameter LNG fire is made up of band emissions of about 50% of energy by water vapor (band emission), about 25% by carbon dioxide and the remainder constituting the continuum emission by luminous soot. The emissions from the H2O and CO2 bands are completely absorbed by the intervening atmosphere in less than about 200 m from the fire, even in the relatively dry desert air. The effective soot radiation constitutes only about 23% during the burning period of methane and increases slightly when other higher hydrocarbon species (ethane, propane, etc.) are

  6. Ultraviolet Studies of Jupiter's Hydrocarbons and Aerosols from Galileo

    Science.gov (United States)

    Gladstone, G. Randall

    2001-01-01

    This is the final report for this project. The purpose of this project was to support PI Wayne Pryor's effort to reduce and analyze Galileo UVS (Ultraviolet Spectrometer) data under the JSDAP program. The spectral observations made by the Galileo UVS were to be analyzed to determine mixing ratios for important hydrocarbon species (and aerosols) in Jupiter's stratosphere as a function of location on Jupiter. Much of this work is still ongoing. To date, we have concentrated on analyzing the variability of the auroral emissions rather than the absorption signatures of hydrocarbons, although we have done some work in this area with related HST-STIS data.

  7. Removal of gasoline vapors from air streams by biofiltration

    Energy Technology Data Exchange (ETDEWEB)

    Apel, W.A.; Kant, W.D.; Colwell, F.S.; Singleton, B.; Lee, B.D.; Andrews, G.F.; Espinosa, A.M.; Johnson, E.G.

    1993-03-01

    Research was performed to develop a biofilter for the biodegradation of gasoline vapors. The overall goal of this effort was to provide information necessary for the design, construction, and operation of a commercial gasoline vapor biofilter. Experimental results indicated that relatively high amounts of gasoline vapor adsorption occur during initial exposure of the biofilter bed medium to gasoline vapors. Biological removal occurs over a 22 to 40{degrees}C temperature range with removal being completely inhibited at 54{degrees}C. The addition of fertilizer to the relatively fresh bed medium used did not increase the rates of gasoline removal in short term experiments. Microbiological analyses indicated that high levels of gasoline degrading microbes are naturally present in the bed medium and that additional inoculation with hydrocarbon degrading cultures does not appreciably increase gasoline removal rates. At lower gasoline concentrations, the vapor removal rates were considerably lower than those at higher gasoline concentrations. This implies that system designs facilitating gasoline transport to the micro-organisms could substantially increase gasoline removal rates at lower gasoline vapor concentrations. Test results from a field scale prototype biofiltration system showed volumetric productivity (i.e., average rate of gasoline degradation per unit bed volume) values that were consistent with those obtained with laboratory column biofilters at similar inlet gasoline concentrations. In addition, total benzene, toluene, ethyl-benzene, and xylene (BTEX) removal over the operating conditions employed was 50 to 55%. Removal of benzene was approximately 10 to 15% and removal of the other members of the BTEX group was much higher, typically >80%.

  8. Removal of gasoline vapors from air streams by biofiltration

    Energy Technology Data Exchange (ETDEWEB)

    Apel, W.A.; Kant, W.D.; Colwell, F.S.; Singleton, B.; Lee, B.D.; Andrews, G.F.; Espinosa, A.M.; Johnson, E.G.

    1993-03-01

    Research was performed to develop a biofilter for the biodegradation of gasoline vapors. The overall goal of this effort was to provide information necessary for the design, construction, and operation of a commercial gasoline vapor biofilter. Experimental results indicated that relatively high amounts of gasoline vapor adsorption occur during initial exposure of the biofilter bed medium to gasoline vapors. Biological removal occurs over a 22 to 40[degrees]C temperature range with removal being completely inhibited at 54[degrees]C. The addition of fertilizer to the relatively fresh bed medium used did not increase the rates of gasoline removal in short term experiments. Microbiological analyses indicated that high levels of gasoline degrading microbes are naturally present in the bed medium and that additional inoculation with hydrocarbon degrading cultures does not appreciably increase gasoline removal rates. At lower gasoline concentrations, the vapor removal rates were considerably lower than those at higher gasoline concentrations. This implies that system designs facilitating gasoline transport to the micro-organisms could substantially increase gasoline removal rates at lower gasoline vapor concentrations. Test results from a field scale prototype biofiltration system showed volumetric productivity (i.e., average rate of gasoline degradation per unit bed volume) values that were consistent with those obtained with laboratory column biofilters at similar inlet gasoline concentrations. In addition, total benzene, toluene, ethyl-benzene, and xylene (BTEX) removal over the operating conditions employed was 50 to 55%. Removal of benzene was approximately 10 to 15% and removal of the other members of the BTEX group was much higher, typically >80%.

  9. Vapor-phase toxicity of butylbenzyl phthalate to three plant species: white mustard, chinese cabbage, and white clover.

    Science.gov (United States)

    Gorsuch, J W; Staples, C A; Brown, D; Enste-Diefenbach, R

    2008-08-01

    During the manufacture of products containing butylbenzyl phthalate (BBP), low emissions to the air may occur. Due to potential exposure of terrestrial communities to BBP vapors, phytotoxicity tests were conducted using Chinese cabbage, white mustard, and white clover. No significant effects on shoot growth were observed at the higher BBP vapor-phase concentration tested, which measured 5.7 microg/m(3). The overall practicality of vapor-phase testing of chemicals with very low vapor pressures is reviewed. These study results suggest that environmental risk from exposure to BBP vapor is negligible for plants.

  10. Estimation of contaminant subslab concentration in petroleum vapor intrusion.

    Science.gov (United States)

    Yao, Yijun; Yang, Fangxing; Suuberg, Eric M; Provoost, Jeroen; Liu, Weiping

    2014-08-30

    In this study, the development and partial validation are presented for an analytical approximation method for prediction of subslab contaminant concentrations in PVI. The method involves combining an analytic approximation to soil vapor transport with a piecewise first-order biodegradation model (together called the Analytic Approximation Method, including Biodegradation, AAMB), the result of which calculation provides an estimate of contaminant subslab concentrations, independent of building operation conditions. Comparisons with three-dimensional (3-D) simulations and another PVI screening tool, BioVapor, show that the AAMB is suitable for application in a scenario involving a building with an impermeable foundation surrounded by open ground surface, where the atmosphere is regarded as the primary oxygen source. Predictions from the AAMB can be used to determine the required vertical source-building separation, given a subslab screening concentration, allowing identification of buildings at risk for PVI. This equation shows that the "vertical screening distance" suggested by U.S. EPA is sufficient in most cases, as long as the total petroleum hydrocarbon (TPH) soil gas concentration at the vapor source does not exceed 50-100mg/L. When the TPH soil gas concentration of the vapor source approaches a typical limit, i.e. 400mg/L, the "vertical screening distance" required would be much greater.

  11. Estimation of contaminant subslab concentration in petroleum vapor intrusion

    Science.gov (United States)

    Yao, Yijun; Yang, Fangxing; Suuberg, Eric M.; Provoost, Jeroen; Liu, Weiping

    2015-01-01

    In this study, the development and partial validation are presented for an analytical approximation method for prediction of subslab contaminant concentrations in PVI. The method involves combining an analytic approximation to soil vapor transport with a piecewise first-order biodegradation model (together called the analytic approximation method, including biodegradation, AAMB), the result of which calculation provides an estimate of contaminant subslab concentrations, independent of building operation conditions. Comparisons with three-dimensional (3-D) simulations and another PVI screening tool, BioVapor, show that the AAMB is suitable for application in a scenario involving a building with an impermeable foundation surrounded by open ground surface, where the atmosphere is regarded as the primary oxygen source. Predictions from the AAMB can be used to determine the required vertical source-building separation, given a subslab screening concentration, allowing identification of buildings at risk for PVI. This equation shows that the “vertical screening distance” suggested by U.S. EPA is sufficient in most cases, as long as the total petroleum hydrocarbon (TPH) soil gas concentration at the vapor source does not exceed 50–100 mg/L. When the TPH soil gas concentration of the vapor source approaches a typical limit, i.e. 400 mg/L, the “vertical screening distance” required would be much greater. PMID:25124892

  12. Do sealless pumps belong in hydrocarbon processing services?

    Energy Technology Data Exchange (ETDEWEB)

    Bennett, Shawn L. [Sundyne Corporation, Arvada, CO (Brazil)

    2004-07-01

    Sealless pump technology seems unimaginable in the hot, dirty and high-pressure world of hydrocarbon processing. Furthermore the high flow rates typical of the industry seem incompatible with sealless pumps. Seals and their environmental controls used in conventional technologies are not immune from these factors making sealless worth another look. In October 2000 the Sealless Centrifugal Pump Specification API 685 was published. This specification lends sealless pumps credibility and emphasizes the proper application of the technology. In many process units seal leaks can be extremely dangerous and costly. The heavy hydrocarbons can auto-ignite and light hydrocarbons will tend to find a source of ignition. The ever-increasing requirements for clean fuels are driving many of the current refinery upgrades. Best Also available control technology requirements and additional focus on Environmental Health and Safety increase the attractiveness of sealless technology to mitigate the hazards associated with seal leaks. Sealless has a place in hydrocarbon processing to eliminate seals, provide mechanical simplification, and ensure personnel/environmental protection. The proper application involves evaluating canned motor/magnetic drive technology, API 685 Guidelines, and vapor pressure versus pump circuit pressure analysis. There are four (4) specific processes where sealless pumps should be targeted: Alkylation, Sulfur Recovery/Hydrotreating, Naphtha Reforming Production, and Neutralization. (author)

  13. One century of air deposition of hydrocarbons recorded in travertine in North Tibetan Plateau, China: Sources and evolution.

    Science.gov (United States)

    Yuan, Guo-Li; Wu, Ming-Zhe; Sun, Yong; Li, Jun; Li, Jing-Chao; Wang, Gen-Hou

    2016-08-01

    The characteristic distribution patterns of hydrocarbons have been used for fingerprinting to identify their sources. The historical air depositions of hydrocarbons recorded in natural media help to understand the evolution of the air environment. Travertine is a natural acceptor of air deposition that settles on the ground layer by layer. To reconstruct the historical air environment of hydrocarbons in the North Tibetan Plateau (NTP), a unique background region, twenty-seven travertine samples were collected systematically from a travertine column according to its precipitated year. For each sample, the precipitated year was dated while n-alkanes and polycyclic aromatic hydrocarbons (PAHs) were determined. Based on source identification, the air environment of hydrocarbons in the past century was studied for the region of NTP. Before World War II, the anthropogenic sources of hydrocarbons showed little influence on the air environment. During World War II and China's War of Liberation, hydrocarbons increased significantly, mainly from the use of fossil fuels. Between 1954 and 1963, hydrocarbons in the air decreased significantly because the sources of petroleum combustion decreased. From the mid-1960s through the end of the 1990s, air hydrocarbons, which mainly originated from biomass burning, increased gradually because agriculture and animal husbandry were developing steadily in Tibet and China. From the late 1990s, hydrocarbons in the atmosphere increased rapidly due to the rapid increase of tourism activities, which might increase hydrocarbon emissions from traffic. The reconstruction of the historical air hydrocarbons in NTP clearly reflects the evolution of the region and global development.

  14. Volatile organic chemical emissions from structural insulated panel (SIP) materials and implications for indoor air quality

    Energy Technology Data Exchange (ETDEWEB)

    Hodgson, Alfred T.

    2003-09-01

    The emissions of volatile organic compounds (VOCs) from structural insulated panel (SIP) materials were investigated. Specimens of newly produced SIPs and associated panel adhesives were obtained from two relatively large manufacturers. Additionally, specimens of the oriented strand board (OSB) used as the inner and outer sheathing and the extruded polystyrene core for the SIP were obtained from one manufacturer. Using small-scale chambers, emissions of formaldehyde, acetaldehyde, acetic acid and other VOCs from SIPs, OSB and polystyrene were measured over a period of four months and from the adhesives over two months. SIP specimens overlaid by gypsum board panels were also tested over four months. The predominant VOCs emitted by the SIPs included acetic acid, pentanal, hexanal and styrene. The emissions of formaldehyde and acetaldehyde were relatively low. Acetic acid and the aldehydes derived from the OSB, while styrene derived from the polystyrene. One of the SIPs emitted toluene and methyl acetate. The adhesives primarily emitted a mixture of hydrocarbons. The emission rates of most VOCs from the SIP/gypsum board assemblies were approximately the same or higher than their respective emission rates from the unfinished SIPs. Modeling using VOC emission factors obtained for the SIP/gypsum board assemblies demonstrated the potential for SIP materials to degrade indoor air quality in houses. A field study to investigate VOC concentrations and emission rates in SIP houses relative to closely matched conventionally constructed houses is necessary to determine the actual impacts of SIPs. If significant impacts are observed, to it may be desirable to develop control measures to reduce the emissions of VOCs from SIPs, such as the substitution of lower emitting materials or the use of vapor diffusion barriers.

  15. Biofiltration of solvent vapors from air

    Energy Technology Data Exchange (ETDEWEB)

    Oh, Young-sook.

    1993-01-01

    For various industrial solvent vapors, biofiltration promises to offer a cost-effective emission control technology. Exploiting the full potential of this technology will help attain the goals of the Clean Air Act Amendments of 1990. Concentrating on large volumes of volatile industrial solvents, stable multicomponent microbial enrichments capable of growing a mineral medium with solvent vapors as their only source of carbon and energy were obtained from soil and sewage sludge. These consortia were immobilized on an optimized porous solid support (ground peat moss and perlite). The biofilter material was packed in glass columns connected to an array of pumps and flow meters that allowed the independent variation of superficial velocity and solvent vapor concentrations. In various experiments, single solvents, such as methanol, butanol, acetonitrile, hexane and nitrobenzene, and solvent mixtures, such as benzene-toluene-xylene (BTX) and chlorobenzene-o-dichlorobenzene (CB/DCB) were biofiltered with rates ranging from 15 to334 g solvent removed per m[sup 3] filter volume /h. Pressure drops were low to moderate (0-10 mmHg/m) and with periodic replacement of moisture, the biofiltration activity could be maintained for a period of several months. The experimental data on methanol biofiltration were subjected to mathematical analysis and modeling by the group of Dr. Baltzis at NJIT for a better understanding and a possible scale up of solvent vapor biofilters. In the case of chlorobenzenes and nitrobenzene, the biofilter columns had to be operated with water recirculation in a trickling filter mode. To prevent inactivation of the trickling filter by acidity during CB/DCB removal, pH control was necessary, and the removal rate of CB/DCB was strongly influenced by the flow rate of the recyling water. Nitrobenzene removal in a trickling filter did not require pH control, since the nitro group was reduced and volatilized as ammonia.

  16. Influence of soil properties on vapor-phase sorption of trichloroethylene

    Energy Technology Data Exchange (ETDEWEB)

    Bekele, Dawit N. [Global Center for Environmental Remediation, University of Newcastle, Callaghan, NSW 2308 (Australia); CRC for Contamination Assessment & Remediation of the Environment, Building X (Environmental Sciences Building), University of South Australia, Mawson Lakes, SA 5095 (Australia); Naidu, Ravi, E-mail: Ravi.Naidu@newcastle.edu.au [Global Center for Environmental Remediation, University of Newcastle, Callaghan, NSW 2308 (Australia); CRC for Contamination Assessment & Remediation of the Environment, Building X (Environmental Sciences Building), University of South Australia, Mawson Lakes, SA 5095 (Australia); Chadalavada, Sreenivasulu [Global Center for Environmental Remediation, University of Newcastle, Callaghan, NSW 2308 (Australia); CRC for Contamination Assessment & Remediation of the Environment, Building X (Environmental Sciences Building), University of South Australia, Mawson Lakes, SA 5095 (Australia)

    2016-04-05

    Highlights: • Vapor intrusion is a major exposure pathway for volatile hydrocarbons. • Certainty in transport processes enhances vapor intrusion model precision. • Detailed understanding of vadose zone vapor transport processes save resources. • Vapor sorption near-steady-state conditions at sites may take months or years. • Type of clay fractions equitably affects sorption of trichloroethylene vapor. - Abstract: Current practices in health risk assessment from vapor intrusion (VI) using mathematical models are based on assumptions that the subsurface sorption equilibrium is attained. The time required for sorption to reach near-steady-state conditions at sites may take months or years to achieve. This study investigated the vapor phase attenuation of trichloroethylene (TCE) in five soils varying widely in clay and organic matter content using repacked columns. The primary indicators of TCE sorption were vapor retardation rate (R{sub t}), the time required for the TCE vapor to pass through the soil column, and specific volume of retention (V{sub R}), and total volume of TCE retained in soil. Results show TCE vapor retardation is mainly due to the rapid partitioning of the compound to SOM. However, the specific volume of retention of clayey soils with secondary mineral particles was higher. Linear regression analyses of the SOM and clay fraction with V{sub R} show that a unit increase in clay fraction results in higher sorption of TCE (V{sub R}) than the SOM. However, partitioning of TCE vapor was not consistent with the samples' surface areas but was mainly a function of the type of secondary minerals present in soils.

  17. A numerical investigation of oxygen concentration dependence on biodegradation rate laws in vapor intrusion.

    Science.gov (United States)

    Yao, Yijun; Shen, Rui; Pennel, Kelly G; Suuberg, Eric M

    2013-12-01

    In subsurface vapor intrusion, aerobic biodegradation has been considered as a major environmental factor that determines the soil gas concentration attenuation factors for contaminants such as petroleum hydrocarbons. The site investigation has shown that oxygen can play an important role in this biodegradation rate, and this paper explores the influence of oxygen concentration on biodegradation reactions included in vapor intrusion (VI) models. Two different three dimensional (3-D) numerical models of vapor intrusion were explored for their sensitivity to the form of the biodegradation rate law. A second order biodegradation rate law, explicitly including oxygen concentration dependence, was introduced into one model. The results indicate that the aerobic/anoxic interface depth is determined by the ratio of contaminant source vapor to atmospheric oxygen concentration, and that the contaminant concentration profile in the aerobic zone was significantly influenced by the choice of rate law.

  18. PM₂.₅-bound polycyclic aromatic hydrocarbons in an area of Rio de Janeiro, Brazil impacted by emissions of light-duty vehicles fueled by ethanol-blended gasoline.

    Science.gov (United States)

    Oliveira, Rafael Lopes; Loyola, Josiane; Minho, Alan Silva; Quiterio, Simone Lorena; de Almeida Azevedo, Débora; Arbilla, Graciela

    2014-12-01

    The aim of this study was to characterize the PM2.5-bound polycyclic aromatic hydrocarbon (PAH) concentrations and their diagnostic ratios in an area impacted by light-duty vehicles fueled by neat ethanol and ethanol-blended gasoline. Samples were collected using a high-volume sampler, extracted, and analyzed for all 16 EPA-priority PAHs using gas chromatography/mass spectrometry (GC/MS) following the EPA 3550B Method. The most abundant PAHs were benzo[g,h,i]perylene, benzo[b]fluoranthene, benzo[a]pyrene and indeno[1,2,3-c,d]pyrene. The total mean concentration was 3.80 ± 2.88 ng m(-3), and the contribution of carcinogenic species was 58 ± 16 % of the total PAHs. The cumulative health hazard from the PAH mixture was determined, and the carcinogenic equivalents and mutagenic equivalents were 0.80 ± 0.82 and 1.17 ± 1.04 ng m(-3), respectively. Diagnostic ratios and normalized ratios were calculated for the individual samples.

  19. Federal Air Pollutant Emission Regulations and Preliminary Estimates of Potential-to-Emit from Biorefineries, Pathway #2: Conversion of Lignocellulosic Biomass to Hydrocarbon Fuels: Fast Pyrolysis and Hydrotreating Bio-oil Pathway

    Energy Technology Data Exchange (ETDEWEB)

    Bhatt, Arpit [National Renewable Energy Lab. (NREL), Golden, CO (United States). Strategic Energy Analysis Center. Technology Systems and Sustainability Analysis Group; Zhang, Yimin [National Renewable Energy Lab. (NREL), Golden, CO (United States). Strategic Energy Analysis Center. Technology Systems and Sustainability Analysis Group; Heath, Garvin [National Renewable Energy Lab. (NREL), Golden, CO (United States). Strategic Energy Analysis Center. Technology Systems and Sustainability Analysis Group; Thomas, Mae [Eastern Research Group, Research Triangle Park, NC (United States); Renzaglia, Jason [Eastern Research Group, Research Triangle Park, NC (United States)

    2017-01-01

    Biorefineries are subject to environmental laws, including complex air quality regulations that aim to protect and improve the quality of the air. These regulations govern the amount of certain types of air pollutants that can be emitted from different types of emission sources. To determine which federal air emission regulations potentially apply to the fast pyrolysis biorefinery, we first identified the types of regulated air pollutants emitted to the ambient environment by the biorefinery or from specific equipment. Once the regulated air pollutants are identified, we review the applicability criteria of each federal air regulation to determine whether the fast pyrolysis biorefinery or specific equipment is subject to it. We then estimate the potential-to-emit of pollutants likely to be emitted from the fast pyrolysis biorefinery to understand the air permitting requirements.

  20. Application of the cubic-plus-association (CPA) equation of state to complex mixtures with aromatic hydrocarbons

    DEFF Research Database (Denmark)

    Folas, Georgios; Kontogeorgis, Georgios; Michelsen, Michael Locht;

    2006-01-01

    The cubic-plus-association (CPA) equation of state is applied to phase equilibria of mixtures containing alcohols, glycols, water, and aromatic or olefinic hydrocarbons. Previously, CPA has been successfully used for mixtures containing various associating compounds (alcohols, glycols, amines......, organic acids, and water) and aliphatic hydrocarbons. We show in this work that the model can be satisfactorily extended to complex vapor-liquid-liquid equilibria with aromatic or olefinic hydrocarbons. The solvation between aromatics/olefinics and polar compounds is accounted for. This is particularly...... of the model (the Soave-Redlich-Kwong (SRK) equation of state) can be obtained from mixtures with aliphatic hydrocarbons. For mixtures of glycols with aromatic hydrocarbons, two parameters have been fitted to experimental data, one in the physical (SRK) part and one in the association part of the model...

  1. An Approach for Developing Site-Specific Lateral and Vertical Inclusion Zones within which Structures Should be Evaluated for Petroleum Vapor Intrusion due to Releases of Motor Fuel from Underground Storage Tanks

    Science.gov (United States)

    Buildings may be at risk from Petroleum Vapor Intrusion (PVI) when they overlie petroleum hydrocarbon contamination in the unsaturated zone or dissolved in groundwater. The U.S. EPA Office of Underground Storage Tanks (OUST) is preparing Guidance for Addressing Petroleum Vapor I...

  2. Hydrocarbon conversion catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Hoek, A.; Huizinga, T.; Maxwell, I.E.

    1989-08-15

    This patent describes a process for hydrocracking hydrocarbon oils into products of lower average molecular weight and lower average boiling point. It comprises contacting a hydrocarbon oil at a temperature between 250{sup 0}C and 500{sup 0}C and a pressure up to 300 bar in the presence of hydrogen with a catalyst consisting essentially of a Y zeolite modified to have a unit cell size below 24.35A, a water absorption capacity (at 25{sup 0}C and a rho/rho/sub o/ value of 0.2) of at least 8% by weight of the zeolite and a pore volume of at least 0.25 ml/g wherein between 10% and 60% of the total pore volume is made up of pores having a diameter of at least 8 nm; an alumina binder and at least one hydrogenation component selected from the group consisting of a Group VI metal, a Group VIII metal and mixtures thereof.

  3. Solvents and vapor intrusion pathways.

    Science.gov (United States)

    Phillips, Scott D; Krieger, Gary R; Palmer, Robert B; Waksman, Javier C

    2004-08-01

    Vapor intrusion must be recognized appropriately as a separate pathway of contamination. Although many issues resemble those of other forms of contamination (particularly its entryway, which is similar to that of radon seepage), vapor intrusion stands apart as a unique risk requiring case-specific action. This article addresses these issues and the current understanding of the most appropriate and successful remedial actions.

  4. Towards Carbon-Neutral CO2 Conversion to Hydrocarbons.

    Science.gov (United States)

    Mattia, Davide; Jones, Matthew D; O'Byrne, Justin P; Griffiths, Owen G; Owen, Rhodri E; Sackville, Emma; McManus, Marcelle; Plucinski, Pawel

    2015-12-07

    With fossil fuels still predicted to contribute close to 80 % of the primary energy consumption by 2040, methods to limit further CO2 emissions in the atmosphere are urgently needed to avoid the catastrophic scenarios associated with global warming. In parallel with improvements in energy efficiency and CO2 storage, the conversion of CO2 has emerged as a complementary route with significant potential. In this work we present the direct thermo-catalytic conversion of CO2 to hydrocarbons using a novel iron nanoparticle-carbon nanotube (Fe@CNT) catalyst. We adopted a holistic and systematic approach to CO2 conversion by integrating process optimization-identifying reaction conditions to maximize conversion and selectivity towards long chain hydrocarbons and/or short olefins-with catalyst optimization through the addition of promoters. The result is the production of valuable hydrocarbons in a manner that can approach carbon neutrality under realistic industrial process conditions.

  5. Toxic compounds emission from fossil fuels in compression with alternative energies

    Energy Technology Data Exchange (ETDEWEB)

    Halek, F.; Kavousi, A. [Dept. of Energy (Iran). Materials and Energy Resesarch Center

    2008-09-30

    Transportation sources are one of the leading contributors to hazardous air pollutants. The internal combustion engine emits a large percentage of pollutants, but gasoline and diesel in the liquid form also contribute chemical pollution in the form of vaporization of the fuel as it heats and cools within the gas tank. Polycyclic aromatic hydrocarbons (PAHs) are a group of organic compounts made up of two or more fused benzene rings in linear, angular or cluster arrangements. PAHs are considered highly toxic for human beings and several of these compounts are carcinogenic, mutagenic or teratogenic. A major source of PAH in Tehran is related to traffic and the number of gasoline and diesel vehicles. During nearly a 1-year period (throughout 2005) a comprehensive study was done in the Tehran area in 21 stations. Results of PAHs analysis indicated that existence of several low molecular weights, like Fluoranthene, Fluorene and Phenantherene confirm the role of diesel oil emissions in Tehran's atmosphere. Biodiesel, a renewable energy source, is the name for a variety of ester-based oxygenated fuels (11% oxygen by weight) made from vegetable oils: sunflower, safflower, soybean, palm, cottonseed, rapeseed or peanut. The lifecycle production and use of biodiesel produces approximately 80% less carbon dioxide emissions, and almost 100% less sulfur dioxide. Combustion of biodiesel alone provides over a 90% reduction in total unburned hydrocarbons, and a 75-90% reduction in aromatic hydrocarbons. Biodiesel further provides significant reductions in particulates and carbon monoxide than petroleum diesel fuel. Based on mutagenicity tests, biodiesel provides a 90% reduction in cancer risks.

  6. Thermophysical Properties of Hydrocarbon Mixtures

    Science.gov (United States)

    SRD 4 NIST Thermophysical Properties of Hydrocarbon Mixtures (PC database for purchase)   Interactive computer program for predicting thermodynamic and transport properties of pure fluids and fluid mixtures containing up to 20 components. The components are selected from a database of 196 components, mostly hydrocarbons.

  7. Hydrocarbon Receptor Pathway in Dogs

    NARCIS (Netherlands)

    Steenbeek, F.G. van; Spee, B.; Penning, L.C.; Kummeling, A.; Gils, I.H.M.; Grinwis, G.C.M.; Leenen, D. van; Holstege, F.C.P.; Vos-Loohuis, M.; Rothuizen, J.; Leegwater, P.A.J.

    2013-01-01

    The aryl hydrocarbon receptor (AHR) mediates biological responses to toxic chemicals. An unexpected role for AHR in vascularization was suggested when mice lacking AHR displayed impaired closure of the ductus venosus after birth, as did knockout mice for aryl hydrocarbon receptor interacting protein

  8. Hydrocarbon Receptor Pathway in Dogs

    NARCIS (Netherlands)

    Steenbeek, F.G. van; Spee, B.; Penning, L.C.; Kummeling, A.; Gils, I.H.M.; Grinwis, G.C.M.; Leenen, D. van; Holstege, F.C.P.; Vos-Loohuis, M.; Rothuizen, J.; Leegwater, P.A.J.

    The aryl hydrocarbon receptor (AHR) mediates biological responses to toxic chemicals. An unexpected role for AHR in vascularization was suggested when mice lacking AHR displayed impaired closure of the ductus venosus after birth, as did knockout mice for aryl hydrocarbon receptor interacting

  9. Vapor phase heat transport systems

    Energy Technology Data Exchange (ETDEWEB)

    Hedstrom, J.C.; Neeper, D.A.

    1985-09-01

    This report describes progress in theoretical and experimental investigations of various forms of a vapor transport system for solar space heating, which could also be applied to service water heating. Refrigerant is evaporated in a solar collector, which may be located on the external wall or roof of a building. The vapor is condensed in a passively discharged thermal storage unit located within the building. The condensed liquid can be returned to the collector either by a motor-driven pump or by a completely passive self-pumping mechanism in which the vapor pressure lifts the liquid from the condenser to the collector. The theoretical investigation analyzes this self-pumping scheme. Experiments in solar test cells compare the operation of both passive and active forms of the vapor system with the operation of a passive water wall. The vapor system operates as expected, with potential advantages over other passive systems in design flexibility and energy yield.

  10. 33 CFR 154.828 - Vapor recovery and vapor destruction units.

    Science.gov (United States)

    2010-07-01

    ... 33 Navigation and Navigable Waters 2 2010-07-01 2010-07-01 false Vapor recovery and vapor... SECURITY (CONTINUED) POLLUTION FACILITIES TRANSFERRING OIL OR HAZARDOUS MATERIAL IN BULK Vapor Control Systems § 154.828 Vapor recovery and vapor destruction units. (a) The inlet to a vapor recovery unit...

  11. Saturn's Stratospheric Water Vapor Distribution

    Science.gov (United States)

    Hesman, B. E.

    2015-12-01

    Water is a sought after commodity in the solar system. It is used as an indication of life, planetary formation timescales, and signatures of past cometary impacts. In Saturn's atmosphere there are two sources of water: an internal primordial reservoir that is confined to the troposphere, and an external source of unknown origin that delivers water to the stratosphere. Potential sources of stratospheric water include: Saturn's main rings (via neutral infall and/or ions transported along magnetic field lines - "Ring Rain"), interplanetary dust particles, and the E-ring that is supplied with water from the plumes of Enceladus. Measuring the latitudinal and seasonal variation of H2O on Saturn will constrain the source of Saturn's stratospheric water. Cassini's Composite InfraRed Spectrometer (CIRS) has detected emission lines of H2O on Saturn at wavelengths of 40 and 50 microns. CIRS also retrieves the temperature of the stratosphere using CH4 lines at 7.7 microns. Using our retrieved temperatures, we derive the mole fraction of H2O at the 0.5-5 mbar level for comparison with water-source models. The latitudinal variation of stratospheric water vapor between 2004-2009 will be presented as a first step in understanding the external source of water on Saturn. The observed local maximum near Saturn's equator supports either a neutral infall from the rings or a source in the E-ring. We will look for secondary maxima at mid-latitudes to determine whether "Ring Rain" also contributes to the inventory of water in Saturn's upper atmosphere.

  12. Vapor pressure measured with inflatable plastic bag

    Science.gov (United States)

    1965-01-01

    Deflated plastic bag in a vacuum chamber measures initial low vapor pressures of materials. The bag captures the test sample vapors and visual observation of the vapor-inflated bag under increasing external pressures yields pertinent data.

  13. A Citizen's Guide to Vapor Intrusion Mitigation

    Science.gov (United States)

    This guide describes how vapor intrusion is the movement of chemical vapors from contaminated soil and groundwater into nearby buildings.Vapors primarily enter through openings in the building foundation or basement walls.

  14. Limitations of microbial hydrocarbon degradation at the Amon mud volcano (Nile deep-sea fan

    Directory of Open Access Journals (Sweden)

    J. Felden

    2013-05-01

    Full Text Available The Amon mud volcano (MV, located at 1250 m water depth on the Nile deep-sea fan, is known for its active emission of methane and non-methane hydrocarbons into the hydrosphere. Previous investigations showed a low efficiency of hydrocarbon-degrading anaerobic microbial communities inhabiting the Amon MV center in the presence of sulfate and hydrocarbons in the seeping subsurface fluids. By comparing spatial and temporal patterns of in situ biogeochemical fluxes, temperature gradients, pore water composition, and microbial activities over 3 yr, we investigated why the activity of anaerobic hydrocarbon degraders can be low despite high energy supplies. We found that the central dome of the Amon MV, as well as a lateral mud flow at its base, showed signs of recent exposure of hot subsurface muds lacking active hydrocarbon degrading communities. In these highly disturbed areas, anaerobic degradation of methane was less than 2% of the methane flux. Rather high oxygen consumption rates compared to low sulfide production suggest a faster development of more rapidly growing aerobic hydrocarbon degraders in highly disturbed areas. In contrast, the more stabilized muds surrounding the central gas and fluid conduits hosted active anaerobic hydrocarbon-degrading microbial communities. The low microbial activity in the hydrocarbon-vented areas of Amon MV is thus a consequence of kinetic limitations by heat and mud expulsion, whereas most of the outer MV area is limited by hydrocarbon transport.

  15. A Lithium Vapor Box similarity experiment employing water vapor

    Science.gov (United States)

    Schwartz, Ja; Jagoe, C.; Goldston, Rj; Jaworski, Ma

    2016-10-01

    Handling high power loads and heat flux in the divertor is a major challenge for fusion power plants. A detached plasma will likely be required. However, hydrogenic and impurity puffing experiments show that detached operation leads easily to X-point MARFEs, impure plasmas, degradation in confinement, and lower helium pressure at the exhaust. The concept of the Lithium Vapor Box Divertor is to use local evaporation and strong differential pumping through condensation to localize the gas-phase material that absorbs the plasma heat flux, and so avoid those difficulties. In order to design such a box first the vapor without plasma must be simulated. The density of vapor required can be estimated using the SOL power, major radius, poloidal box length, and cooling energy per lithium atom. For an NSTX-U-sized machine, the Knudsen number Kn spans 0.01 to 1, the transitional flow regime. This regime cannot handled by fluid codes or collisionless Monte Carlo codes, but can be handled by Direct Simulation Monte Carlo (DSMC) codes. To validate a DSMC model, we plan to build a vapor box test stand employing more-convenient water vapor instead of lithium vapor as the working fluid. Transport of vapor between the chambers at -50C will be measured and compared to the model. This work supported by DOE Contract No. DE-AC02-09CH11466.

  16. An equation of state for property prediction of alcohol-hydrocarbon and water-hydrocarbon systems

    Energy Technology Data Exchange (ETDEWEB)

    Pires, Adolfo P. [Laboratory of Petroleum Engineering and Exploration, Universidade Estadual do Norte Fluminense-UENF, RJ Macae (Brazil); Mohamed, Rahoma S. [Process Engineering Laboratory, School of Chemical Engineering, Universidade Estadual de Campinas, Unicamp, Caixa Postal 6066, 13083-970 SP Campinas (Brazil); Ali Mansoori, G. [Department of Chemical Engineering, University of Illinois at Chicago, 810 S. Clinton Street, 60607-7000 Chicago, IL (United States)

    2001-12-29

    Equations of state have been widely used in the petroleum and chemical industries for thermodynamic property calculation. In the presence of polar substances that self-associate through hydrogen bonding (such as water or alcohol), equations of state are of very limited use. One way to account for the association is to consider the equation of state to be formed of two contributions: physical and chemical. In this work, we develop an equation of state consisting of two terms as proposed by Andreko [Fluid Phase Equilib. 65 (1991) 89], a chemical and a physical term, for correlation of thermodynamic properties of mixtures containing an associating species. This equation of state is used to correlate vapor pressure data for a number of associating molecules, such as alcohol and water, as well as bubble point pressure data for binary water-hydrocarbon and alcohol-hydrocarbon systems. The results obtained are in good agreement with the experimental data and requiring the use of only one adjustable parameter for each binary system.

  17. Statistical Analysis of the Phase 3 Emissions Data Collected in the EPAct/V2/E89 Program: January 7, 2010 - July 6, 2012

    Energy Technology Data Exchange (ETDEWEB)

    Gunst, R. F.

    2013-05-01

    Phase 3 of the EPAct/V2/E-89 Program investigated the effects of 27 program fuels and 15 program vehicles on exhaust emissions and fuel economy. All vehicles were tested over the California Unified Driving Cycle (LA-92) at 75 degrees F. The program fuels differed on T50, T90, ethanol, Reid vapor pressure, and aromatics. The vehicles tested were new, low-mileage 2008 model year Tier 2 vehicles. A total of 956 test runs were made. Comprehensive statistical modeling and analyses were conducted on methane, carbon dioxide, carbon monoxide, fuel economy, non-methane hydrocarbons, non-methane organic gases, oxides of nitrogen, particulate matter, and total hydrocarbons. In general, model fits determined that emissions and fuel economy were complicated by functions of the five fuel parameters. An extensive evaluation of alternative model fits produced a number of competing model fits. Many of these alternative fits produce similar estimates of mean emissions for the 27 program fuels but should be carefully evaluated for use with emerging fuels with combinations of fuel parameters not included here. The program includes detailed databases on each of the 27 program fuels on each of the 15 vehicles and on each of the vehicles on each of the program fuels.

  18. Increase in the performance of vapor plants using gas turbines in series; Aumento da eficiencia de usinas a vapor utilizando turbinas a gas em serie

    Energy Technology Data Exchange (ETDEWEB)

    Lezuo, Alex [Siemens AG (Brazil)

    1991-12-31

    An interesting option to improve the power efficiency of a conventional vapor plant is to convert it in a combined vapor and gas plant, coupling a gas series turbine. The investment is relatively low, the investment return time is short, and the low specific fuel consumption makes it possible to save in the general cost of the operation. At the same time, the quantity of residues to be disposed and also the pollutants emission are drastically reduced 5 refs., 3 figs., 2 tabs.

  19. Program plan for the resolution of tank vapor issues

    Energy Technology Data Exchange (ETDEWEB)

    Osborne, J.W.; Huckaby, J.L.

    1994-05-01

    Since 1987, workers at the Hanford Site waste tank farms in Richland, Washington, have reported strong odors emanating from the large, underground high-level radioactive waste storage tanks. Some of these workers have complained of symptoms (e.g., headaches, nausea) related to the odors. In 1992, the U.S. Department of Energy, which manages the Hanford Site, and Westinghouse Hanford Company determined that the vapor emissions coming from the tanks had not been adequately characterized and represented a potential health risk to workers in the immediate vicinity of the tanks. At that time, workers in certain areas of the tank farms were required to use full-face, supplied-breathing-air masks to reduce their exposure to the fugitive emissions. While use of supplied breathing air reduced the health risks associated with the fugitive emissions, it introduced other health and safety risks (e.g., reduced field of vision, air-line tripping hazards, and heat stress). In 1992, an aggressive program was established to assure proper worker protection while reducing the use of supplied breathing air. This program focuses on characterization of vapors inside the tanks and industrial hygiene monitoring in the tank farms. If chemical filtration systems for mitigation of fugitive emissions are deemed necessary, the program will also oversee their design and installation. This document presents the plans for and approach to resolving the Hanford Site high-level waste tank vapor concerns. It is sponsored by the Department of Energy Office of Environmental Restoration and Waste Management.

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

    Science.gov (United States)

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

  1. A two-dimensional analytical model of petroleum vapor intrusion

    Science.gov (United States)

    Yao, Yijun; Verginelli, Iason; Suuberg, Eric M.

    2016-02-01

    In this study we present an analytical solution of a two-dimensional petroleum vapor intrusion model, which incorporates a steady-state diffusion-dominated vapor transport in a homogeneous soil and piecewise first-order aerobic biodegradation limited by oxygen availability. This new model can help practitioners to easily generate two-dimensional soil gas concentration profiles for both hydrocarbons and oxygen and estimate hydrocarbon indoor air concentrations as a function of site-specific conditions such as source strength and depth, reaction rate constant, soil characteristics and building features. The soil gas concentration profiles generated by this new model are shown in good agreement with three-dimensional numerical simulations and two-dimensional measured soil gas data from a field study. This implies that for cases involving diffusion dominated soil gas transport, steady state conditions and homogenous source and soil, this analytical model can be used as a fast and easy-to-use risk screening tool by replicating the results of 3-D numerical simulations but with much less computational effort.

  2. Calculation of Interfacial Tensions of Hydrocarbon-water Systems under Reservoir Conditions

    DEFF Research Database (Denmark)

    Zuo, You-Xiang; Stenby, Erling Halfdan

    1998-01-01

    Assuming that the number densities of each component in a mixture are linearly distributed across the interface between the coexisting vapor-liquid or liquid-liquid phases, we developed in this research work a linear-gradient-theory (LGT) model for computing the interfacial tension of hydrocarbon......-brine systems. The new model was tested on a number of hydrocarbon-water/brine mixtures and two crude oil-water systems under reservoir conditions. The results show good agreement between the predicted and the experimental interfacial tension data....

  3. Design and Use of a Full Flow Sampling System (FFS) for the Quantification of Methane Emissions.

    Science.gov (United States)

    Johnson, Derek R; Covington, April N; Clark, Nigel N

    2016-06-12

    The use of natural gas continues to grow with increased discovery and production of unconventional shale resources. At the same time, the natural gas industry faces continued scrutiny for methane emissions from across the supply chain, due to methane's relatively high global warming potential (25-84x that of carbon dioxide, according to the Energy Information Administration). Currently, a variety of techniques of varied uncertainties exists to measure or estimate methane emissions from components or facilities. Currently, only one commercial system is available for quantification of component level emissions and recent reports have highlighted its weaknesses. In order to improve accuracy and increase measurement flexibility, we have designed, developed, and implemented a novel full flow sampling system (FFS) for quantification of methane emissions and greenhouse gases based on transportation emissions measurement principles. The FFS is a modular system that consists of an explosive-proof blower(s), mass airflow sensor(s) (MAF), thermocouple, sample probe, constant volume sampling pump, laser based greenhouse gas sensor, data acquisition device, and analysis software. Dependent upon the blower and hose configuration employed, the current FFS is able to achieve a flow rate ranging from 40 to 1,500 standard cubic feet per minute (SCFM). Utilization of laser-based sensors mitigates interference from higher hydrocarbons (C2+). Co-measurement of water vapor allows for humidity correction. The system is portable, with multiple configurations for a variety of applications ranging from being carried by a person to being mounted in a hand drawn cart, on-road vehicle bed, or from the bed of utility terrain vehicles (UTVs). The FFS is able to quantify methane emission rates with a relative uncertainty of ± 4.4%. The FFS has proven, real world operation for the quantification of methane emissions occurring in conventional and remote facilities.

  4. Description and History of the MOBILE Highway Vehicle Emission Factor Model

    Science.gov (United States)

    MOBILE is an EPA model for estimating pollution from highway vehicles. It has been superseded by the Motor Vehicle Emission Simulator (MOVES). MOBILE calculates emissions of hydrocarbons (HC), oxides of nitrogen (NOx) and carbon monoxide (CO).

  5. The reformation of liquid hydrocarbons in an aqueous discharge reactor

    KAUST Repository

    Zhang, Xuming

    2015-04-21

    We present an aqueous discharge reactor for the reformation of liquid hydrocarbons. To increase a dielectric constant of a liquid medium, we added distilled water to iso-octane and n-dodecane. As expected, we found decreased discharge onset voltage and increased discharge power with increased water content. Results using optical emission spectroscopy identified OH radicals and O atoms as the predominant oxidative reactive species with the addition of water. Enriched CH radicals were also visualized, evidencing the existence of cascade carbon-carbon cleavage and dehydrogenation processes in the aqueous discharge. The gaseous product consisted primarily of hydrogen, carbon monoxide, and unsaturated hydrocarbons. The composition of the product was readily adjustable by varying the volume of water added, which demonstrated a significant difference in composition with respect to the tested liquid hydrocarbon. In this study, we found no presence of CO2 emissions or the contamination of the reactor by solid carbon deposition. These findings offer a new approach to the reforming processes of liquid hydrocarbons and provide a novel concept for the design of a practical and compact plasma reformer. © 2015 IOP Publishing Ltd.

  6. Hydrocarbon characterization experiments in fully turbulent fires.

    Energy Technology Data Exchange (ETDEWEB)

    Ricks, Allen; Blanchat, Thomas K.

    2007-05-01

    As the capabilities of numerical simulations increase, decision makers are increasingly relying upon simulations rather than experiments to assess risks across a wide variety of accident scenarios including fires. There are still, however, many aspects of fires that are either not well understood or are difficult to treat from first principles due to the computational expense. For a simulation to be truly predictive and to provide decision makers with information which can be reliably used for risk assessment the remaining physical processes must be studied and suitable models developed for the effects of the physics. The model for the fuel evaporation rate in a liquid fuel pool fire is significant because in well-ventilated fires the evaporation rate largely controls the total heat release rate from the fire. A set of experiments are outlined in this report which will provide data for the development and validation of models for the fuel regression rates in liquid hydrocarbon fuel fires. The experiments will be performed on fires in the fully turbulent scale range (> 1 m diameter) and with a number of hydrocarbon fuels ranging from lightly sooting to heavily sooting. The importance of spectral absorption in the liquid fuels and the vapor dome above the pool will be investigated and the total heat flux to the pool surface will be measured. The importance of convection within the liquid fuel will be assessed by restricting large scale liquid motion in some tests. These data sets will provide a sound, experimentally proven basis for assessing how much of the liquid fuel needs to be modeled to enable a predictive simulation of a fuel fire given the couplings between evaporation of fuel from the pool and the heat release from the fire which drives the evaporation.

  7. Reduction of vaporous emissions during transport of petrol and mineral oil products by river tank ships (20. BImSchV); Verminderung gasfoermiger Emissionen beim Transport von Ottokraftstoffen und Mineraloelprodukten mit Binnenschiffen (20. BImSchV)

    Energy Technology Data Exchange (ETDEWEB)

    Schaefer, K.; Hoffmann, H.; Emeis, S.; Jahn, C.; Sedlmaier, A.; Wilhelm, H.; Dormuth, I.

    2001-11-01

    The gas-free ventilation of the tanks of river tank ships by the common praxis to ventilate the tank atmosphere into ambient air is a big emission source of VOCs and a strong deterioration of air quality. It was shown during several measurement campaigns that the ventilation of the tank atmosphere of river tank ships via the loading / unloading pipes into the land-site vapour recovery unit is a technical solution. The measured emission source strengths during this type of ventilation are of the same amount as the measured emission source strengths during loading and unloading of petrol and are caused by attachment and detachment of loading / unloading pipes only. Furthermore, the concentrations of petrol in the tank atmosphere were measured by the PTB during these experiments. As result of the investigations a leaflet as instruction of environment friendly ventilation of tank atmosphere of river tank ships for the inland sailors and operators of tank storage plants was composed. On the basis of an inquiry of the available vapour recovery units the required capacity of land-site vapour recovery units for the replacement of all ventilation of tank atmosphere to open air was estimated. The capacity of the available vapour recovery units is too low for a preferably short time period of tank atmosphere ventilation. Solving this problem not only the enhancement of the capacity of the available vapour recovery units up to a capacity of 2,200 m{sup 3}/h must be considered but their availability at loading / unloading points of petrol as well as the availability of berthing place must be taken into account also. The necessary enhancement of the capacity and the number of possible new installations of vapour recovery units cannot be defined now because a new amendment for the execution of the 20. BImSchV came into force on 25 August 2001 which allows the ventilation of tank atmosphere of river tank ships to open air under certain conditions until 31 December 2005. To draw

  8. Joule-Thomson Inversion in Vapor-Liquid-Solid Solution Systems

    Science.gov (United States)

    Nichita, Dan Vladimir; Pauly, Jerome; Daridon, Jean-Luc

    2009-07-01

    Solid phase precipitation can greatly affect thermal effects in isenthalpic expansions; wax precipitation may occur in natural hydrocarbon systems in the range of operating conditions, the wax appearance temperature being significantly higher (as high as 350 K) for hyperbaric fluids. Recently, methods for calculating the Joule-Thomson inversion curve (JTIC) for two-phase mixtures, and for three-phase vapor-liquid-multisolid systems have been proposed. In this study, an approach for calculating the JTIC for the vapor-liquid-solid solution systems is presented. The JTIC is located by tracking extrema and angular points of enthalpy departure variations versus pressure at isothermal conditions. The proposed method is applied to several complex synthetic and naturally occurring hydrocarbon systems. The JTIC can exhibit several distinct branches (which may lie within two- or three-phase regions or follow phase boundaries), multiple inversion temperatures at fixed pressure, as well as multiple inversion pressures at given temperature.

  9. Spinning dust emission from ultrasmall silicates: emissivity and polarization spectrum

    CERN Document Server

    Hoang, Thiem; Lan, Nguyen Quynh

    2016-01-01

    Anomalous microwave emission (AME) is an important Galactic foreground of Cosmic Microwave Background (CMB) radiation. It is believed that the AME arises from rotational emission by spinning polycyclic aromatic hydrocarbons (PAHs) in the interstellar medium (ISM). In this paper, we assume that a population of ultrasmall silicate grains may exist in the ISM, and quantify rotational emissivity from these tiny particles and its polarization spectrum. We found that spinning silicate nanoparticles can produce strong rotational emission when those small grains follow a log-normal size distribution. The polarization fraction of spinning dust emission from tiny silicates increases with decreasing the dipole moment per atom ($\\beta$) and can reach $P\\sim 20\\%$ for $\\beta\\sim 0.1$D at grain temperature of 60 K. We identify a parameter space $(\\beta,Y_{Si})$ for silicate nanoparticles in which its rotational emission can adequately reproduce both the observed AME and the polarization of the AME, without violating the ob...

  10. Calculation of emissions into rivers in Germany using the MONERIS model. Nutrients, heavy metals and polycyclic aromatic hydrocarbons; Berechnung von Stoffeintraegen in die Fliessgewaesser Deutschlands mit dem Modell MONERIS. Naehrstoffe, Schwermetalle und Polyzyklische aromatische Kohlenwasserstoffe

    Energy Technology Data Exchange (ETDEWEB)

    Fuchs, Stephan; Scherer, Ulrike; Wander, Ramona [Karlsruher Institut fuer Technologie, Karlsruhe (Germany). Inst. fuer Wasser und Gewaesserentwicklung; Behrendt, Horst; Venohr, Markus; Optiz, Dieter [Leibniz-Institut fuer Gewaesseroekologie und Binnenfischerei im Forschungsverbund Berlin e.V., Berlin (Germany); Hillenbrand, Thomas; Marscheider-Weidemann, Frank; Goetz, Thomas [Fraunhofer-Institut fuer System- und Innovationsforschung, Karlsruhe (Germany)

    2010-09-15

    The aim of both projects was a methodological development of the MONERIS model to quantify emissions from point and diffuse sources into Germany's surface waters. Both projects are based on consistent sub-basins and the according basic data as well as homogenous calculation algorithms that are adapted to the specifications of each substance group. The research encompasses Germany's large river basins as well as their catchment areas outside Germany and in total covers an area of 650,000 km{sup 2}. This was divided into 3456 analytical units (2759 of those in Germany), the average catchment areas being 190 km{sup 2} (135 km{sup 2} in Germany). All input data was collected and preprocessed with the highest spatial and temporal resolution possible based on the detailed topology. The modelling was performed in individual annual steps for the period between 1983-2005. For the evaluation of the temporal trends the data was aggregated for the periods 1983-1987 (''1985''), 1993-1997 (''1995''), 1998-2002 (''2000'') and 2003-2005 (''2005'') to soften the impact of hydrological influences. The basic data and model results for all sub-basins, years and substance groups of both projects were merged into one database. Additionally, a web-based graphical user interface was developed to visualise the emissions for any area aggregation can be visualised. The completion of both projects delivered for the first time ever homogenous instruments that can identify the most important sources and contamination hotspots for different relevant substance groups in larger river basins which can then serve as a basis for further analyses to achieve efficient measures to reduce pollution. (orig.)

  11. Multiwavelength Strontium Vapor Lasers

    Science.gov (United States)

    Soldatov, A. N.; Yudin, N. A.

    2016-08-01

    Based on an analysis of experimental and theoretical works, modern notion on conditions of forming of population density inversion on self-terminating IR transitions of alkali-earth metals is given. It is demonstrated that there is a significant difference in the inversion formation in lasers on self-terminating transitions in the visible and near-IR ranges and lasers on self-terminating transitions of alkali-earth metals lasing IR lines in the mid-IR range. It is shown that in the discharge circuit of lasers on self-terminating metal atom transitions (LSMT) there are processes strengthening the influence of the known mechanism limiting the frequency and energy characteristics (FEC) of radiation caused by the presence of prepulse electron concentration. The mechanism of influence of these processes on FEC of the LSMT and technical methods of their neutralization are considered. The possibility of obtaining average lasing power of ~200 W from one liter volume of the active medium of the strontium vapor laser is demonstrated under conditions of neutralization of these processes.

  12. Archimedes Mass Filter Vaporizer

    Science.gov (United States)

    Putvinski, S.; Agnew, A. F.; Cluggish, B. P.; Ohkawa, T.; Sevier, L.; Umstadter, K. R.; Dresvin, S. V.; Kuteev, B. V.; Feygenson, O. N.; Ivanov, D. V.; Zverev, S. G.; Miroshnikov, I. V.; Egorov, S. M.; Kiesewetter, D. V.; Maliugin, V. I.

    2001-10-01

    Archimedes Technology Group, Inc., is developing a plasma mass separator called the Archimedes Filter that separates waste oxide mixtures ion by ion into two mass groups: light and heavy. Since high-level waste at Hanford has 99.9its radioactivity associated with heavy elements, the Archimedes Filter can effectively decontaminate over three-quarters of that waste. The Filter process involves some preprocessing followed by volatilization and separation by the magnetic and electric fields of the main plasma. This presentation describes the approach to volatilization of the waste oxy-hydroxide mixture by means of a very high heat flux (q > 10 MW/m2). Such a high heat flux is required to ensure congruent evaporation of the complex oxy-hydroxide mixture and is achieved by injection of small droplets of molten waste into an inductively coupled plasma (ICP) torch. This presentation further addresses different issues related to evaporation of the waste including modeling of droplet evaporation, estimates of parameters of plasma torch, and 2D modeling of the plasma. The experimental test bed for oxide vaporization and results of the initial experiments on oxide evaporation in 60 kW ICP torch will also be described.

  13. Biodegradation studies of oil sludge containing high hydrocarbons concentration

    Energy Technology Data Exchange (ETDEWEB)

    Olguin-Lora, P.; Munoz-Colunga, A.; Castorena-Cortes, G.; Roldan-Carrillo, T.; Quej Ake, L.; Reyes-Avila, J.; Zapata-Penasco, I.; Marin-Cruz, J.

    2009-07-01

    Oil industry has a significant impact on environment due to the emission of, dust, gases, waste water and solids generated during oil production all the way to basic petrochemical product manufacturing stages. the aim of this work was to evaluate the biodegradation of sludge containing high hydrocarbon concentration originated by a petroleum facility. A sludge sampling was done at the oil residuals pool (ORP) on a gas processing center. (Author)

  14. Reduction of vaporous emissions during transport of petrol and mineral oil products by river tank ships (20. BImSchV); Verminderung gasfoermiger Emissionen beim Transport von Ottokraftstoffen und Mineraloelprodukten mit Binnenschiffen (20. BImSchV)

    Energy Technology Data Exchange (ETDEWEB)

    Schaefer, K.; Hoffmann, H.; Emeis, S.; Jahn, C.; Sedlmaier, A.; Wilhelm, H.; Dormuth, I.

    2001-11-01

    The gas-free ventilation of the tanks of river tank ships by the common praxis to ventilate the tank atmosphere into ambient air is a big emission source of VOCs and a strong deterioration of air quality. It was shown during several measurement campaigns that the ventilation of the tank atmosphere of river tank ships via the loading / unloading pipes into the land-site vapour recovery unit is a technical solution. The measured emission source strengths during this type of ventilation are of the same amount as the measured emission source strengths during loading and unloading of petrol and are caused by attachment and detachment of loading / unloading pipes only. Furthermore, the concentrations of petrol in the tank atmosphere were measured by the PTB during these experiments. As result of the investigations a leaflet as instruction of environment friendly ventilation of tank atmosphere of river tank ships for the inland sailors and operators of tank storage plants was composed. On the basis of an inquiry of the available vapour recovery units the required capacity of land-site vapour recovery units for the replacement of all ventilation of tank atmosphere to open air was estimated. The capacity of the available vapour recovery units is too low for a preferably short time period of tank atmosphere ventilation. Solving this problem not only the enhancement of the capacity of the available vapour recovery units up to a capacity of 2,200 m{sup 3}/h must be considered but their availability at loading / unloading points of petrol as well as the availability of berthing place must be taken into account also. The necessary enhancement of the capacity and the number of possible new installations of vapour recovery units cannot be defined now because a new amendment for the execution of the 20. BImSchV came into force on 25 August 2001 which allows the ventilation of tank atmosphere of river tank ships to open air under certain conditions until 31 December 2005. To draw

  15. Infrared emission from interstellar PAHs

    Science.gov (United States)

    Allamandola, L. J.; Tielens, A. G. G. M.; Barker, J. R.

    1987-01-01

    The mid-IR absorption and Raman spectra of polycyclic aromatic hydrocarbons (PAHs) and the mechanisms determining them are reviewed, and the implications for observations of similar emission spectra in interstellar clouds are considered. Topics addressed include the relationship between PAHs and amorphous C, the vibrational spectroscopy of PAHs, the molecular emission process, molecular anharmonicity, and the vibrational quasi-continuum. Extensive graphs, diagrams, and sample spectra are provided, and the interstellar emission bands are attributed to PAHs with 20-30 C atoms on the basis of the observed 3.3/3.4-micron intensity ratios.

  16. Vapor Intrusion Facilities - South Bay

    Data.gov (United States)

    U.S. Environmental Protection Agency — POINT locations for the South Bay Vapor Instrusion Sites were derived from the NPL data for Region 9. One site, Philips Semiconductor, was extracted from the...

  17. Understanding Latent Heat of Vaporization.

    Science.gov (United States)

    Linz, Ed

    1995-01-01

    Presents a simple exercise for students to do in the kitchen at home to determine the latent heat of vaporization of water using typical household materials. Designed to stress understanding by sacrificing precision for simplicity. (JRH)

  18. Modeling vapor dominated geothermal reservoirs

    Energy Technology Data Exchange (ETDEWEB)

    Marconcini, R.; McEdwards, D.; Neri, G.; Ruffilli, C.; Schroeder, R.; Weres, O.; Witherspoon, P.

    1977-09-12

    The unresolved questions with regard to vapor-dominated reservoir production and longevity are reviewed. The simulation of reservoir behavior and the LBL computer program are discussed. The geology of Serrazzano geothermal field and its reservoir simulation are described. (MHR)

  19. Modulation of urinary polycyclic aromatic hydrocarbon metabolites by enzyme polymorphisms in workers of the German Human Bitumen Study.

    Science.gov (United States)

    Rihs, Hans-Peter; Spickenheuer, Anne; Heinze, Evelyn; Pesch, Beate; Raulf-Heimsoth, Monika; Angerer, Jürgen; Brüning, Thomas

    2011-06-01

    Data concerning the influence of sequence variants of metabolizing enzymes on the effect modulation of current exposure to vapors and aerosols of bitumen in humans are limited. To assess the influence of 18 single-nucleotide polymorphisms (SNP) in genes coding for enzymes involved in polycyclic aromatic hydrocarbon (PAH) and amine metabolism regarding their impact on urinary markers 1-hydroxpyrene (1-OHP) and the sum of 1-, 2+9-, 3-, 4-hydroxyphenanthrene (OHPHE). Based on personal ambient monitoring data for bitumen emissions, 218 German workers exposed to vapors and aerosols of bitumen during a shift and 96 German roadside construction workers without exposure to bitumen but with similar working tasks were studied. SNP determination based on DNA aliquots isolated from blood samples by real-time PCR or direct sequencing. The impact of sequence variants on the urinary levels of 1-OHP and sum of OHPHE was estimated with mixed linear models, adjusted for age, creatinine, exposure, smoking, SNP, and time of measurement. In the mixed linear model, an increasing metabolite level of OHPHE was only slightly modulated by the CC variant of the cytochrome P450 SNP CYP1A1 3801T>C (rs4646903; P = 0.051). In contrast, GSTM1 carriers showed a significant (P= 0.046) and double-mutated variants of three NAT2-specific SNP (NAT2*341CC, P = 0.06; NAT2*481TT, P = 0.06; NAT2*803GG, P = 0.042) displayed a decreasing influence on OHPHE levels. None of the SNP studied showed a significant effect on 1-OHP. The modulating SNP effects on OHPHE in the adjusted model were less pronounced when compared with the effects observed in a recent study with 170 workers occupationally exposed to PAH in German industries. This may be due to the much lower PAH exposure in the Human Bitumen Study.

  20. Comprehensive management of hydrocarbon storage tanks ageing

    Energy Technology Data Exchange (ETDEWEB)

    Lesueur, V.; Riethmuller, M.; Chauveau, D. [IS Services, Villepinte (France)

    2006-07-01

    Corrosion generates considerable material losses in industry and can result in irreversible damages to the environment and some times in losses in human lives. Hydrocarbon storage tanks are subject to various corrosion types like generalised corrosion resulting in large areas thickness reduction, or potentially dangerous local damage (pitting, crevice or craters). To keep safe storage conditions and save service life, it is essential: - to identify the risks by taking into account the stored products, the storage type, the environmental factors, the type of coating and the storage history, - to select the most appropriate NDT technique (acoustic emission, thickness ultrasonic measurement, TOFD, ACFM, visual inspection, remote UT..) depending on the part to be inspected and on the expected type of damage, - to propose the best solution for storage tank restoration (repair, improved protection..) - to modify the operating conditions - to define the NDT periodicity and the appropriate technique to apply according to the type of risks, to the former inspection results and to the regulation context, - to determine the remaining life of storage tank. This approach is named Comprehensive Management of hydrocarbon storage tank ageing. IS Services has developed a software called ''AGIR'' aiming at providing guidance and support to apply this approach. (orig.)

  1. Hydrocarbon Leak Detection Sensor Project

    Data.gov (United States)

    National Aeronautics and Space Administration — FTT is proposing the development of a sensor to detect the presence of hydrocarbons in turbopump Inter-Propellant Seals (IPS). The purpose of the IPS is to prevent...

  2. Growth of hydrocarbon utilizing microorganisms

    Digital Repository Service at National Institute of Oceanography (India)

    Bhosle, N.B.; Mavinkurve, S.

    Two isolates from marine mud having broad spectrum hydrocarbon utilizing profile were identified as Arthrobacter simplex and Candida tropicalis.Both the organisms grew exponentially on crude oil. The cell yield of the organisms was influenced...

  3. UV Discharge Lamp on Alcohol Vapor

    Science.gov (United States)

    Avtaeva, Svetlana; Heneral, Andrij

    2009-10-01

    The non coherent sources of UV radiation based on safe and nontoxic gaseous mixtures have good aspects for different applications. The paper reports about experimental investigations of the high voltage capacitive discharge in alcohol vapor. The time-integrated emission spectra have been studied in the wavelength interval from 200 to 400 nm at alcohol vapor pressure of 1 Torr. In the spectra the most intensive bands were vibrational bands of the CO(b->a) transition with heads at 283.3 (0-0), 297.7 (0-1), 313.4 (0-2), 330.5 (0-3) and 349.3 nm (0-4). The (0-2) band of CO molecules superimposes with (0-0) and (1-1) vibrational bands of the CH(C->X) transition with Q-heads at 314.49 and 315.66 nm on the long wavelength side and with bands of OH radicals with intensity maximums at 308.1 and 309.2 nm (A->X transition) on the short wavelength side. No other radiating species were detected. The emitting surface area of the lamp is 220 cm^2, average output power of the UV radiation is 70 mW and the estimated efficiency is 0.2%. This source of UV radiation can be applied in photochemistry, in medicine, for disinfection of medical tools, in ecology and for purification and disinfection of water from different pathogenic microorganisms.

  4. The contribution of polycyclic aromatic hydrocarbon fractions with different boiling ranges to the carcinogenic impact of emission condensate from coal fired residential furnaces as evaluated by topical application to the skin of mice.

    Science.gov (United States)

    Grimmer, G; Brune, H; Deutsch-Wenzel, R; Dettbarn, G; Misfeld, J; Abel, U; Timm, J

    1985-09-15

    Flue gas condensate from briquet-fired residential furnaces was separated into a polycyclic aromatic compound (PAC)-free and a PAC-containing part, followed by a subfractionation of the PAC-containing fraction into 3 parts: PAC consisting predominantly of (a) 2 and 3 rings, (b) 4 and 5 rings and (c) 6 and more rings. To evaluate the carcinogenic potency of the condensate and its fractions, local application onto skin of mice in 2 or 3 doses was used. Since it was known from an earlier investigation that both the PAC-free fraction and the fraction containing PAC with 2 and 3 rings were almost ineffective, only PAC-fractions containing more than 3 rings were tested. The probit and Weibull analysis of the results showed that the condensate and the fractions containing PAC with 4 and 5 rings as well as 6 and more rings provoke local tumors after repeated application to the dorsal skin of mice. The tumor incidence exhibited a clear cut dose-response relationship. Fractions (b) and (c) were almost equally active, each contributing by about 50% to the total carcinogenicity. The content of benzo[a]pyrene (0.72 mg/g condensate) contributed by 10-11% to the total carcinogenicity of the emission.

  5. A geração química de vapor em espectrometria atômica Chemical vapor generation in atomic spectrometry

    Directory of Open Access Journals (Sweden)

    Iracema Takase

    2002-12-01

    Full Text Available The historical development of atomic spectrometry techniques based on chemical vapor generation by both batch and flow injection sampling formats is presented. Detection via atomic absorption spectrometry (AAS, microwave induced plasma optical emission spectrometry (MIP-OES, inductively coupled plasma optical emission spectrometry (ICP-OES , inductively coupled plasma mass spectrometry (ICP-MS and furnace atomic nonthermal excitation spectrometry (FANES are considered. Hydride generation is separately considered in contrast to other methods of generation of volatile derivatives. Hg ¾ CVAAS (cold vapor atomic absorption spectrometry is not considered here. The current state-of-the-art, including extension, advantages and limitations of this approach is discussed.

  6. Dispensing fuel with aspiration of condensed vapors

    Energy Technology Data Exchange (ETDEWEB)

    Butkovich, M.S.; Strock, D.J.

    1993-08-10

    A vapor recovery process is described, comprising the steps of: fueling a motor vehicle with gasoline by discharging gasoline into a fill opening or filler pipe of a tank of said vehicle through a fuel outlet conduit of a nozzle; emitting gasoline vapors from said tank during said fueling; substantially collecting said vapors during said fueling with a vapor return conduit of said nozzle and passing said vapors through said vapor return conduit in counter current flow relationship to said discharging gasoline in said fuel conduit; conveying said vapors from said vapor return conduit to a vapor return hose; at least some of said vapors condensing to form condensate in said vapor return hose; substantially removing said condensate from said vapor return hose during said fueling with a condensate pickup tube from said nozzle by passing said condensate through said condensate pickup tube in counter current flow relationship to said conveying vapors in said vapor return hose; sensing the presence of gasoline with a liquid sensing tube in said vapor return conduit of said nozzle between inner and outer spouts of said nozzle to detect when said tank of said vehicle is filled with said fuel conduit being within the inner spout of said nozzle; and automatically shutting off said fueling and condensate removing when said liquid sensing tube detects when said tank of said vehicle is filled and fuel enters said vapor return conduit.

  7. Bioassay of polycyclic aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Van Kirk, E.A.

    1980-08-01

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

  8. Electrochemical decomposition of chlorinated hydrocarbons

    OpenAIRE

    McGee, Gerard Anthony

    1993-01-01

    This work involves the characterisation of the electrochemical decomposition of chlorinated hydrocarbons. A variety of methods were employed involving the use of catalytic reagents to enhance the rate at which chlorinated organic compounds are reduced. The first reagent used was oxygen which was electrochemically reduced to superoxide in nonaqueous solvents. Superoxide is a reactive intermediate and decomposes chlorinated hydrocarbons. However it was found that since the rate of reaction betw...

  9. Aliphatic hydrocarbons of the fungi.

    Science.gov (United States)

    Weete, J. D.

    1972-01-01

    Review of studies of aliphatic hydrocarbons which have been recently detected in the spores of phytopathogenic fungi, and are found to be structurally very similar to the alkanes of higher plants. It appears that the hydrocarbon components of the few mycelial and yeast forms reported resemble the distribution found in bacteria. The occurence and distribution of these compounds in the fungi is discussed. Suggested functional roles of fungal spore alkanes are presented.

  10. LIQUID HYDROCARBON FUEL CELL DEVELOPMENT.

    Science.gov (United States)

    A compound anode consists of a reforming catalyst bed in direct contact with a palladium-silver fuel cell anode. The objective of this study was to...prove the feasibility of operating a compound anode fuel cell on a liquid hydrocarbon and to define the important parameters that influence cell...performance. Both reformer and fuel cell tests were conducted with various liquid hydrocarbon fuels. Included in this report is a description of the

  11. Kinetics of wet sodium vapor complex plasma

    Science.gov (United States)

    Mishra, S. K.; Sodha, M. S.

    2014-04-01

    In this paper, we have investigated the kinetics of wet (partially condensed) Sodium vapor, which comprises of electrons, ions, neutral atoms, and Sodium droplets (i) in thermal equilibrium and (ii) when irradiated by light. The formulation includes the balance of charge over the droplets, number balance of the plasma constituents, and energy balance of the electrons. In order to evaluate the droplet charge, a phenomenon for de-charging of the droplets, viz., evaporation of positive Sodium ions from the surface has been considered in addition to electron emission and electron/ion accretion. The analysis has been utilized to evaluate the steady state parameters of such complex plasmas (i) in thermal equilibrium and (ii) when irradiated; the results have been graphically illustrated. As a significant outcome irradiated, Sodium droplets are seen to acquire large positive potential, with consequent enhancement in the electron density.

  12. Combustion performance and heat transfer characterization of LOX/hydrocarbon type propellants. Task 3: Data dump

    Science.gov (United States)

    Hart, S. W.

    1982-01-01

    A preliminary characterization of Orbital Maneuvering System (OMS) and Reaction Control System (RCS) engine point designs over a range of thrust and chamber pressure for several hydrocarbon fuels is reported. OMS and RCS engine point designs were established in two phases comprising baseline and parametric designs. Interface pressures, performance and operating parameters, combustion chamber cooling and turboprop requirements, component weights and envelopes, and propellant conditioning requirements for liquid to vapor phase engine operation are defined.

  13. HYDROCARBONS RESERVES IN VENEZUELA

    Energy Technology Data Exchange (ETDEWEB)

    Gonzalez Cruz, D.J.

    2007-07-01

    Venezuela is an important player in the energy world, because of its hydrocarbons reserves. The process for calculating oil and associated gas reserves is described bearing in mind that 90% of the gas reserves of Venezuela are associated to oil. Likewise, an analysis is made of the oil reserves figures from 1975 to 2003. Reference is also made to inconsistencies found by international experts and the explanations offered in this respect by the Ministry of Energy and Petroleum (MENPET) and Petroleos de Venezuela (PDVSA) regarding the changes that took place in the 1980s. In turn, Hubbert's Law is explained to determine peak production of conventional oil that a reservoir or field will reach, as well as its relationship with remaining reserves. Emphasis is placed on the interest of the United Nations on this topic. The reserves of associated gas are presented along with their relationship with the different crude oils that are produced and with injected gas, as well as with respect to the possible changes that would take place in the latter if oil reserves are revised. Some recommendations are submitted so that the MENPET starts preparing the pertinent policies ruling reserves. (auth)

  14. Evaluation of hydrocarbon potential

    Energy Technology Data Exchange (ETDEWEB)

    Cashman, P.H.; Trexler, J.H. Jr. [Univ. of Nevada, Reno, NV (United States)

    1992-09-30

    Task 8 is responsible for assessing the hydrocarbon potential of the Yucca Mountain vincinity. Our main focus is source rock stratigraphy in the NTS area in southern Nevada. (In addition, Trexler continues to work on a parallel study of source rock stratigraphy in the oil-producing region of east central Nevada, but this work is not funded by Task 8.) As a supplement to the stratigraphic studies, we are studying the geometry and kinematics of deformation at NTS, particularly as these pertain to reconstructing Paleozoic stratigraphy and to predicting the nature of the Late Paleozoic rocks under Yucca Mountain. Our stratigraphic studies continue to support the interpretation that rocks mapped as the {open_quotes}Eleana Formation{close_quotes} are in fact parts of two different Mississippian units. We have made significant progress in determining the basin histories of both units. These place important constraints on regional paleogeographic and tectonic reconstructions. In addition to continued work on the Eleana, we plan to look at the overlying Tippipah Limestone. Preliminary TOC and maturation data indicate that this may be another potential source rock.

  15. Optofluidic reactors for reverse combustion photocatalytic production of hydrocarbons (Conference Presentation)

    Science.gov (United States)

    Schein, Perry; Erickson, David

    2017-03-01

    In combustion, hydrocarbon fuels are burned with oxygen to release energy, carbon dioxide and water vapor. Here, we introduce a photocatalytic reactor for reversing this process, when carbon dioxide and water are combined and using optical and thermal energy from the sun hydrocarbons are produced and oxygen is released. This allows for the sustainable production of hydrocarbon products from non-fossil sources, allowing for the development of "green" hydrocarbon products. Our reactors take the form of modular cells of 10 x 10 x 10 cm scale where light is delivered to nanostructured catalysts through the evanescent field around dielectric slab waveguides. The light distribution is optimized through the use of engineered scattering sites to enhance field uniformity. This is combined with integrated fluidic architecture to deliver a stream rich in water and carbon dioxide (such as exhaust from a natural gas burning plant) to the nanostructured catalyst particles in a narrow channel. Exhaust streams rich in oxygen and hydrocarbon products are collected at the outlet of the reactor cell. The cell is heated using solar thermal energy and temperatures of up to 200°C are achieved, enhancing reaction efficiency. Hydrocarbon products produced include methanol as well as other potentially useful molecules for fuel production or precursors to the manufacture of plastics. These reactors can be coupled to solar collectors to take advantage of the sun as a free source of heat and light, and the modular nature of the cells enables scaling to larger deployments.

  16. Atmospheric polycyclic aromatic hydrocarbons in Seoul, Korea

    Science.gov (United States)

    Park, Seung S.; Kim, Young J.; Kang, Chang H.

    Daily particulate- and vapor-phase polycyclic aromatic hydrocarbons (PAH) samples were collected at an urban site in Seoul, Korea, during five intensive sampling campaigns between October 1998 and December 1999. PAH samples collected on quartz fiber filters and PUF plugs were first extracted using dichloromethane with ultrasonication and supercritical fluid extraction methods, respectively, and then analyzed by GC/MSD/SIM. Seasonal trends in atmospheric PAH concentrations in the study area were highly influenced by fossil fuel usage for domestic heating, boundary layer height, and air temperature. The relative benzo[a]pyrene amount and particulate organic to elemental carbon ratio calculated from the measurement results suggested that photo-oxidation is not an important factor in the variation of PAH concentrations during the summer sampling periods. Correlation studies between specific PAH of the individual factors identified by principal component factor analysis and meteorological parameters revealed that both temperature and relative humidity gave greater effects on the semi-volatile PAH, PHEN and FLT, rather than on the heavier PAH, B(b+k)F and BghiP.

  17. A device for reforming a hydrocarbon fuel

    Energy Technology Data Exchange (ETDEWEB)

    Kendzi, T.; Ikuo, M.

    1984-03-15

    In order to utilize the heat from the reaction of reforming of a hydrocarbon fuel and the heat scattered from a heater, a design is proposed for a fuel reforming reactor in which the gases entering the reactor first pass inside the reactor along the external wall and are heated by the heat dispersed inside the reactor. Then they go in the opposite direction along a clearance between the interior shell of the reactor and the internal body of the reactor itself with a catalyst (Kt) and a heated electrical cylindrical heater. Then the gases, already heated, go directly into the cavity of the reactor filled with the catalyst where the reforming reaction occurs and then the gases and the vapors of the reformed fuel are discharged, passing through a system of heat exchangers. The layout of such a reactor, which contains a cylindrical shell inside, a cylindrical sleeve coaxial with it and the body of the reactor itself with the heater, is given. A system for attaching the internal sleeve and the body of the reactor to the catalyst is cited. The course of the gases inside the reactor is also given.

  18. U.S. Strategic Petroleum Reserve Vapor Pressure Committee 2009 annual report.

    Energy Technology Data Exchange (ETDEWEB)

    Allen, Ray (Allen Energy Services, Inc., Longview, TX); Eldredge, Lisa (DynMcDermott Petroleum Operations, Harahan, LA); DeLuca, Charles (DynMcDermott Petroleum Operations, Harahan, LA); Mihalik, Patrick (DynMcDermott Petroleum Operations, Harahan, LA); Maldonado, Julio (U.S. Department of Energy, Harahan, LA); Lord, David L.; Rudeen, David Keith (GRAM, Inc., Albuquerque, NM); Berndsen, Gerard (U.S. Department of Energy, Harahan, LA)

    2010-05-01

    This report comprises an annual summary of activities under the U.S. Strategic Petroleum Reserve (SPR) Vapor Pressure Committee in FY2009. The committee provides guidance to senior project management on the issues of crude oil vapor pressure monitoring nd mitigation. The principal objectives of the vapor pressure program are, in the event of an SPR drawdown, to minimize the impact on the environment and assure worker safety and public health from crude oil vapor emissions. The annual report reviews key program areas ncluding monitoring program status, mitigation program status, new developments in measurements and modeling, and path forward including specific recommendations on cavern sampling for the next year. The contents of this report were first presented to SPR senior anagement in December 2009, in a deliverable from the vapor pressure committee. The current SAND report is an adaptation for the Sandia technical audience.

  19. An interim reference model for the variability of the middle atmosphere water vapor distribution

    Science.gov (United States)

    Remsberg, E. E.; Russell, J. M., III; Wu, C.-Y.

    1990-01-01

    A reference model for the middle atmosphere water vapor distribution for some latitudes and seasons was developed using two data sets. One is the seven months of Nimbus LIMS data obtained during November 1978 to May 1979 over the range 64 deg S - 84 deg N latitude and from about 100-mb to 1-mb altitude, and the other is represented by water vapor profiles from 0.2 mb to 0.01 mb in the mid-mesosphere, measured on ground at several fixed mid-latitude sites in the Northern Hemisphere, using microwave-emission techniques. This model provides an interim water vapor profile for the entire vertical range of the middle atmosphere, with accuracies of better than 25 percent. The daily variability of stratospheric water vapor profiles about the monthly mean is demonstrated, and information is provided on the longitudinal variability of LIMS water vapor profiles about the daily, weekly, and monthly zonal means.

  20. A Review of Vapor Intrusion Models

    OpenAIRE

    Yao, Yijun; Suuberg, Eric M.

    2013-01-01

    A complete vapor intrusion (VI) model, describing vapor entry of volatile organic chemicals (VOCs) into buildings located on contaminated sites, generally consists of two main parts-one describing vapor transport in the soil and the other its entry into the building. Modeling the soil vapor transport part involves either analytically or numerically solving the equations of vapor advection and diffusion in the subsurface. Contaminant biodegradation must often also be included in this simulatio...

  1. Recent advances in vapor intrusion site investigations.

    Science.gov (United States)

    McHugh, Thomas; Loll, Per; Eklund, Bart

    2017-02-22

    Our understanding of vapor intrusion has evolved rapidly since the discovery of the first high profile vapor intrusion sites in the late 1990s and early 2000s. Research efforts and field investigations have improved our understanding of vapor intrusion processes including the role of preferential pathways and natural barriers to vapor intrusion. This review paper addresses recent developments in the regulatory framework and conceptual model for vapor intrusion. In addition, a number of innovative investigation methods are discussed.

  2. Relating tropical ocean clouds to moist processes using water vapor isotope measurements

    OpenAIRE

    J. Lee; Worden, J.; D. Noone; K. Bowman; A. Eldering; A. LeGrande; Li, J.-L. F.; Schmidt, G; Sodemann, H.

    2010-01-01

    We examine the co-variations of tropospheric water vapor, its isotopic composition and cloud types and relate these distributions to tropospheric mixing and distillation models using satellite observations from the Aura Tropospheric Emission Spectrometer (TES) over the summertime tropical ocean. Interpretation of these process distributions must take into account the sensitivity of the TES isotope and water vapor measurements to variations in cloud, water, and temperature amount. Consequently...

  3. Tank 241-TY-104 vapor sampling and analysis tank characterization report

    Energy Technology Data Exchange (ETDEWEB)

    Huckaby, J.L.

    1995-05-31

    This report presents the details of the Hanford waste tank characterization study for tank 241-TY-104. The drivers and objectives of the headspace vapor sampling and analysis were in accordance with procedures that were presented in other reports. The vapor and headspace gas samples were collected and analyzed to determine the potential risks to tank farm workers due to fugitive emissions from the tank.

  4. Determination of vapor pressures for nonpolar and semipolar organic compounds from gas chromatographic retention data

    Science.gov (United States)

    Hinckley, D.A.; Bidleman, T.F.; Foreman, W.T.; Tuschall, J.R.

    1990-01-01

    Vapor pressures for nonpolar and moderately polar organochlorine, pyrethroid, and organophosphate insecticides, phthalate esters, and organophosphate flame retardants were determined by capillary gas chromatography (GC). Organochlorines and polycyclic aromatic hydrocarbons with known liquid-phase vapor pressures (P??L) (standard compounds) were chromatographed along with two reference compounds n-C20 (elcosane) and p,p???-DDT on a 1.0-m-long poly(dimethylsiloxane) bonded-phase (BP-1) column to determine their vapor pressures by GC (P??GC). A plot of log P??L vs log P??GC for standard compounds was made to establish a correlation between measured and literature values, and this correlation was then used to compute P??L of test compounds from their measured P??GC. P??L of seven major components of technical chlordane, endosulfan and its metabolites, ??-hexachlorocyclohexane, mirex, and two components of technical toxaphene were determined by GC. This method provides vapor pressures within a factor of 2 of average literature values for nonpolar compounds, similar to reported interlaboratory precisions of vapor pressure determinations. GC tends to overestimate vapor pressures of moderately polar compounds. ?? 1990 American Chemical Society.

  5. Fixed-bed Adsorption Characteristics of Chlorinated Hydrocarbon Vapors onto Hydrophobic Hypercrosslinked Polymeric Resin%疏水性超高交联吸附树脂对氯代烃蒸气的固定床吸附特性研究

    Institute of Scientific and Technical Information of China (English)

    于伟华; 刘鹏; 龙超; 陶为华

    2011-01-01

    The dynamic adsorption of trichloroethylene(TCE),1,2-dichloroethane(DCE) and trichloromethane(TCM) vapors onto hydrophobic hypercrosslinked polymeric resin(LC-1) were investigated using the fixed-bed adsorption method.The results indicated that the breakthrough time decreased and the height of mass transfer zone increased with the elevated initial concentration,gas flow rate and adsorption temperature.The gas flow rate had the wost significant influence on breakthrough time and height of mass transfer zone among the three factors.In addition,a simple semi-empirical mathematic model developed by Yoon and Nelson was applied to investigate the breakthrough behavior,and all correlation coefficients R2 were greater than 0.994.%采用固定床吸附法研究了三氯乙烯(TCE)、1,2-二氯乙烷(DCE)和三氯甲烷(TCM)共3种氯代烃类蒸气在疏水性超高交联吸附树脂LC-1上的动态吸附行为.结果表明,TCE、DCE和TCM蒸气的初始浓度、气体流速和吸附温度均会影响动态吸附过程,随着初始浓度、气体流速和吸附温度的增大,穿透时间变短,传质区长度增大,其中气体流速的影响最大;采用半经验数学模型Yoon-Nelson模型对吸附穿透实验数据进行拟合,拟合相关性系数R2≥0.994.

  6. Thermal performance of direct contact heat exchangers for mixed hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Sharpe, L. Jr.; Coswami, D.Y.; Demuth, O.J.; Mines, G.

    1985-01-01

    This paper describes a physical and a mathematical model for evaluating the tray efficiencies for a direct contact heat exchanger (DCHX). The model is then used to determine the efficiencies for tests conducted on a 60kW sieve tray DCHX as heat is transferred from a geofluid (brine) to a working fluid (mixed hydrocarbons). It is assumed that there are three distinct regions in the column based on the state of the working fluid, as follows: Region I - Preheating with no vaporization; Region II - Preheating with moderate vaporization; and Region III - Major vaporization. The boundaries of these regions can be determined from the experimental data. In the model, mass balance and energy balance is written for a tray ''N'' in each of these regions. Finally, the ''tray efficiency'' or ''heat transfer'' effectiveness of the tray is calculated based on the definition that it is the ratio of the actual heat transfer to the maximum possible, thermodynamically.

  7. Exposure assessment modeling for volatiles--towards an Australian indoor vapor intrusion model.

    Science.gov (United States)

    Turczynowicz, Leonid; Robinson, Neville I

    2007-10-01

    Human health risk assessment of sites contaminated by volatile hydrocarbons involves site-specific evaluations of soil or groundwater contaminants and development of Australian soil health-based investigation levels (HILs). Exposure assessment of vapors arising from subsurface sources includes the use of overseas-derived commercial models to predict indoor air concentrations. These indoor vapor intrusion models commonly consider steady-state assumptions, infinite sources, limited soil biodegradation, negligible free phase, and equilibrium partitioning into air and water phases to represent advective and diffusive processes. Regional model construct influences and input parameters affect model predictions while steady-state assumptions introduce conservatism and jointly highlight the need for Australian-specific indoor vapor intrusion assessment. An Australian non-steady-state indoor vapor intrusion model has been developed to determine cumulative indoor human doses (CIHDs) and to address these concerns by incorporating Australian experimental field data to consider mixing, dilution, ventilation, sink effects and first-order soil and air degradation. It was used to develop provisional HILs for benzene, toluene, ethylbenzene, and xylene (BTEX), naphthalene, and volatile aliphatic and aromatic total petroleum hydrocarbons (TPH) < or = EC16 fractions for crawl space dwellings. This article summarizes current state of knowledge and discusses proposed research for differing exposure scenarios based on Australian dwelling and subsurface influences, concurrent with sensitivity analyses of input parameters and in-field model validation.

  8. Distribution of multi-component solvents in solvent vapor extraction chamber

    Energy Technology Data Exchange (ETDEWEB)

    Das, S. [Society of Petroleum Engineers, Richardson, TX (United States)]|[Marathon Oil Corp., Houston, TX (United States)

    2008-10-15

    Vapex process performance is sensitive to operating pressures, temperatures and the types of solvent used. The hydrocarbon solvents used in Vapex processes typically have between 5 and 10 per cent hydrocarbon impurities, and the accumulation of dense phases inside the vapor chamber reduces gravity drainage potential. This study investigated the partitioning of solvent compounds inside the vapor chamber during in situ Vapex processes.The aim of the study was to examine how the different components of the mixed solvent partitioned inside the extracted chamber during the oil and vapor phase. A 2-D homogenous reservoir model was used to simulate the Vapex process with a solvent mixture comprised of propane and methane at various percentages. The effect of injecting a hot solvent vapor was also investigated. The study showed that injected methane accumulated at both the top and the extraction interface. Accumulations near the top had a positive impact on solvent confinement in thin reservoirs. Diffusion of the solvent component was controlled by gas phase molecular diffusion, and was much faster than the diffusion of solvent molecules in the liquid phase. The use of hot solvent mixtures slowed the extraction process due to lower solvent solubility in the oil phase. It was concluded that the negative impact on viscosity reduction by dilution was not compensated by rises in temperature. 6 refs., 11 figs.

  9. Fabrication of PECVD-grown fluorinated hydrocarbon nanoparticles and circular nanoring arrays using nanosphere lithography

    Energy Technology Data Exchange (ETDEWEB)

    Sarkar, D.K. [Industrial Chair on Atmospheric Icing of Power Network Equipment (CIGELE) and Canada Research Chair on Atmospheric Icing Engineering of Power Networks (INGIVRE) at Universite du Quebec a Chicoutimi, Quebec (Canada)], E-mail: dsarkar@uqac.ca; Farzaneh, M. [Industrial Chair on Atmospheric Icing of Power Network Equipment (CIGELE) and Canada Research Chair on Atmospheric Icing Engineering of Power Networks (INGIVRE) at Universite du Quebec a Chicoutimi, Quebec (Canada)

    2008-04-30

    Nanosphere lithography (NSL) masks were created by spin-coating of polystyrene particles onto silicon surfaces. Fluorinated hydrocarbon films were coated on the nanosphere lithography masks using plasma-enhanced chemical vapor deposition (PECVD) to obtain ordered arrays of fluorinated hydrocarbon. Atomic force microscope images show hexagonally ordered nanodots of dimension 225 {+-} 11 nm with a height of 23 {+-} 4 nm. Every hexagon encloses a circular ring of diameter 540 {+-} 24 nm having a height and width of 13.5 {+-} 0.6 nm and 203 {+-} 16 nm, respectively. FTIR analysis shows two distinct zones of atomic bonding of CH{sub x} and CF{sub x} in the plasma coated ordered fluorinated hydrocarbon films.

  10. Tank 241-BY-107 vapor sampling and analysis tank characterization report

    Energy Technology Data Exchange (ETDEWEB)

    Huckaby, J.L.

    1995-05-05

    Tank 241-BY-107 headspace gas and vapor samples were collected and analyzed to help determine the potential risks to tank farm workers due to fugitive emissions from the tank. The drivers and objectives of waste tank headspace sampling and analysis are discussed in {open_quotes}Program Plan for the Resolution of Tank Vapor Issues{close_quotes}. Tank 241-BY-107 was vapor sampled in accordance with {open_quotes}Data Quality Objectives for Generic In-Tank Health and Safety Issue Resolution{close_quotes}.

  11. Tank 241-BY-107 vapor sampling and analysis tank characterization report. Revision 1

    Energy Technology Data Exchange (ETDEWEB)

    Huckaby, J.L.

    1995-05-31

    Tank 241-BY-107 headspace gas and vapor samples were collected and analyzed to help determine the potential risks to tank farm workers due to fugitive emissions from the tank. The drivers and objectives of waste tank headspace sampling and analysis are discussed in {open_quotes}Program Plan for the Resolution of Tank Vapor Issues.{close_quotes} Tank 241-BY-107 was vapor sampled in accordance with {open_quotes}Data Quality Objectives for Generic In-Tank Health and Safety Issue Resolution.{close_quotes}

  12. Tank 241-BY-108 vapor sampling and analysis tank characterization report. Revision 1

    Energy Technology Data Exchange (ETDEWEB)

    Huckaby, J.L.

    1995-05-31

    Tank 241-BY-108 headspace gas and vapor samples were collected and analyzed to help determine the potential risks to tank farm workers due to fugitive emissions from the tank. The drivers and objectives of waste tank headspace sampling and analysis are discussed in ``Program Plan for the Resolution of Tank Vapor Issues`` (Osborne and Huckaby 1994). Tank 241-BY-108 was vapor sampled in accordance with ``Data Quality Objectives for Generic In-Tank Health and Safety Issue Resolution (Osborne et al., 1994).

  13. The long-term evolution of hydrocarbons in Jupiter's stratosphere

    Science.gov (United States)

    Melin, Henrik; Fletcher, Leigh N.; Greathouse, Thomas K.; Giles, Rohini Sara; Sinclair, James; Orton, Glenn S.; Irwin, Patrick Gerard Joseph

    2016-10-01

    We present the global distribution of hydrocarbons in Jupiter's stratosphere using ground-based mid-infrared R~15,000 TEXES observations from the NASA Infrared Telescope Facility (IRTF), obtained between 2013 and 2016. Ethane and acetylene are the primary products of methane photolysis in Jupiter's stratosphere, and their spatial distribution can be used to trace atmospheric circulation and the lifetimes of chemical constituents. Zonal mean distributions of these species have been previously studied from the Voyager and Cassini spacecraft (Nixon et al., 2010, doi: 10.1016/j.pss.2010.05.008), but the TEXES dataset now provides the opportunity to track the evolution of the hydrocarbons from Earth (Fletcher et al., 2016, doi:10.1016/j.icarus.2016.06.008 ). Global spectral maps of methane, ethane and acetylene emission are used to characterize the temporal evolution of large scale features in Jupiter's stratosphere (0.5-20 mbar?), including: equator to pole contrasts driven by large-scale stratospheric overturning; mid-latitude bands of elevated hydrocarbon emission; small-scale wave phenomena driven by meteorological activity in the underlying troposphere; and the tropical changes in emission related to Jupiter's Quasi-Quadrennial Oscillation. The NEMESIS spectral inversion tool (Irwin et al., 2008, doi: 10.1016/j.jqsrt.2007.11.006) is used to derive stratospheric temperatures and hydrocarbon abundances from spatially-resolved spectra at 744, 819, and 1247 cm-1. We use these to investigate the changes in the vertical temperature and ethane and acetylene distributions over time, with the aim of providing the global and temporal context for Juno's exploration of the jovian atmosphere in 2016/17.

  14. Electrochemical NOx Sensor for Monitoring Diesel Emissions

    Energy Technology Data Exchange (ETDEWEB)

    Woo, L Y; Glass, R S

    2008-11-14

    Increasingly stringent emissions regulations will require the development of advanced gas sensors for a variety of applications. For example, compact, inexpensive sensors are needed for detection of regulated pollutants, including hydrocarbons (HCs), CO, and NO{sub x}, in automotive exhaust. Of particular importance will be a sensor for NO{sub x} to ensure the proper operation of the catalyst system in the next generation of diesel (CIDI) automobiles. Because many emerging applications, particularly monitoring of automotive exhaust, involve operation in harsh, high-temperature environments, robust ceramic-oxide-based electrochemical sensors are a promising technology. Sensors using yttria-stabilized zirconia (YSZ) as an oxygen-ion-conducting electrolyte have been widely reported for both amperometric and potentiometric modes of operation. These include the well-known exhaust gas oxygen (EGO) sensor. More recently, ac impedance-based (i.e., impedance-metric) sensing techniques using YSZ have been reported for sensing water vapor, hydrocarbons, CO, and NO{sub x}. Typically small-amplitude alternating signal is applied, and the sensor response is measured at a specified frequency. Most impedance-metric techniques have used the modulus (or magnitude) at low frequencies (< 1 Hz) as the sensing signal and attribute the measured response to interfacial phenomena. Work by our group has also investigated using phase angle as the sensing signal at somewhat higher frequencies (10 Hz). The higher frequency measurements would potentially allow for reduced sampling times during sensor operation. Another potential advantage of impedance-metric NO{sub x} sensing is the similarity in response to NO and NO{sub 2} (i.e., total-NO{sub x} sensing). Potentiometric NO{sub x} sensors typically show higher sensitivity to NO2 than NO, and responses that are opposite in sign. However, NO is more stable than NO{sub 2} at temperatures > 600 C, and thermodynamic calculations predict {approx}90

  15. Stage 2 vapor recovery system

    Energy Technology Data Exchange (ETDEWEB)

    Koch, W.H.; Strock, D.J.; Butkovich, M.S.; Hartman, H.B.

    1993-05-25

    A vapor recovery system is described, comprising: a set of elongated underground storage tanks, each storage tank containing a different grade of gasoline; vent pipes; a series of dispensing units; fuel flow lines; vapor return lines; an array of fuel pumps for pumping gasoline from said storage tanks to said dispenser units; an elongated condensate liquid pickup tube; an elongated inner spout providing a fuel conduit and having an outer tip defining a fuel outlet for discharging gasoline into a filler pipe of a motor vehicle tank during fueling; an outer spout assembly; extending into and engaging said spout-receiving socket, said outer spout assembly comprising an outer spout providing a vapor return conduit and defining apertures providing a vapor inlet spaced from said fuel outlet for withdrawing, removing, and returning a substantial amount of gasoline vapors emitted during said fueling; an elongated liquid sensing tube; a manually operable level; a flow control valve assembly; an automatic shutoff valve assembly; and a venturi sleeve assembly positioned in said venturi sleeve receiving chamber.

  16. The Lithium Vapor Box Divertor

    Science.gov (United States)

    Goldston, Robert; Hakim, Ammar; Hammett, Gregory; Jaworski, Michael; Myers, Rachel; Schwartz, Jacob

    2015-11-01

    Projections of scrape-off layer width to a demonstration power plant suggest an immense parallel heat flux, of order 12 GW/m2, which will necessitate nearly fully detached operation. Building on earlier work by Nagayama et al. and by Ono et al., we propose to use a series of differentially pumped boxes filled with lithium vapor to isolate the buffering vapor from the main plasma chamber, allowing stable detachment. This powerful differential pumping is only available for condensable vapors, not conventional gases. We demonstrate the properties of such a system through conservation laws for vapor mass and enthalpy, and then include plasma entrainment and ultimately an estimate of radiated power. We find that full detachment should be achievable with little leakage of lithium to the main plasma chamber. We also present progress towards solving the Navier-Stokes equation numerically for the chain of vapor boxes, including self-consistent wall boundary conditions and fully-developed shocks, as well as concepts for an initial experimental demonstration-of-concept. This work supported by DOE Contract No. DE-AC02-09CH11466.

  17. Benzodiazepine-like discriminative stimulus effects of toluene vapor.

    Science.gov (United States)

    Shelton, Keith L; Nicholson, Katherine L

    2013-11-15

    In vitro studies show that the abused inhalant toluene affects a number of ligand-gated ion channels.The two most consistently implicated of these are γ-aminobutyric acid type A(GABAA) receptors which are positively modulated by toluene and N-methyl-D-aspartate(NMDA) receptors which are negatively modulated by toluene. Behavioral studies also suggest an interaction of toluene with GABAA and/or NMDA receptors but it is unclear if these receptors underlie the abuse-related intoxicating effects of toluene. Seventeen B6SJLF1/J mice were trained using a two-choice operant drug discrimination procedure to discriminate 10 min of exposure to 2000 ppm toluene vapor from 10 min of exposure to air. The discrimination was acquired in a mean of 65 training sessions. The stimulus effects of 2000 ppm toluene vapor were exposure concentration-dependent but rapidly diminished following the cessation of vapor exposure. The stimulus effects of toluene generalized to the chlorinated hydrocarbon vapor perchloroethylene but not 1,1,2-trichloroethane nor the volatile anesthetic isoflurane. The competitive NMDA antagonist CGS-19755, the uncompetitive antagonist dizocilpine and the glycine-site antagonist L701,324 all failed to substitute for toluene. The classical nonselective benzodiazepines midazolam and chlordiazepoxide produced toluene-like stimulus effects but the alpha 1 subunit preferring positive GABAA modulator zaleplon failed to substitute for toluene. The barbiturates pentobarbital and methohexital and the GABAA positive modulator neurosteroid allopregnanolone did not substitute for toluene. These data suggest that the stimulus effects of toluene may be at least partially mediated by benzodiazepine-like positive allosteric modulation of GABAA receptors containing alpha 2, 3 or 5 subunits.

  18. Method of depositing a high-emissivity layer

    Science.gov (United States)

    Wickersham, Charles E.; Foster, Ellis L.

    1983-01-01

    A method of depositing a high-emissivity layer on a substrate comprising RF sputter deposition of a carbide-containing target in an atmosphere of a hydrocarbon gas and a noble gas. As the carbide is deposited on the substrate the hydrocarbon gas decomposes to hydrogen and carbon. The carbon deposits on the target and substrate causing a carbide/carbon composition gradient to form on the substrate. At a sufficiently high partial pressure of hydrocarbon gas, a film of high-emissivity pure carbon will eventually form over the substrate.

  19. Behavior of vapor/plasma within the keyhole and above the workpiece during CO2 laser penetration welding

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    In this paper, a high-speed camera and an optical emission monitor were used to study the behavior of vapor/plasma during CO2 laser welding of SUS304 stainless steel. Results of optical emission from vapor/plasma show that two characteristic frequency bands exist, 100-500 Hz and 1 500-3 500 Hz. At the same time, the changing images of vapor/plasma and bottom pool also confirm that there are two different fluctuation frequency bands. One of the frequency bands represents the characteristic of vapor/plasma within the keyhole, and it is within 167-500 Hz. Another frequency band is within 1 500-3 500 Hz, and it obviously derives from the shielding gas. Some factors may cause these frequency differences between the keyhole plasma and the shielding gas plasma. One of them is that the vapor/plasma pressure within the keyhole will increase slowly.

  20. Chemical Kinetics of Hydrocarbon Ignition in Practical Combustion Systems

    Energy Technology Data Exchange (ETDEWEB)

    Westbrook, C.K.

    2000-07-07

    Chemical kinetic factors of hydrocarbon oxidation are examined in a variety of ignition problems. Ignition is related to the presence of a dominant chain branching reaction mechanism that can drive a chemical system to completion in a very short period of time. Ignition in laboratory environments is studied for problems including shock tubes and rapid compression machines. Modeling of the laboratory systems are used to develop kinetic models that can be used to analyze ignition in practical systems. Two major chain branching regimes are identified, one consisting of high temperature ignition with a chain branching reaction mechanism based on the reaction between atomic hydrogen with molecular oxygen, and the second based on an intermediate temperature thermal decomposition of hydrogen peroxide. Kinetic models are then used to describe ignition in practical combustion environments, including detonations and pulse combustors for high temperature ignition, and engine knock and diesel ignition for intermediate temperature ignition. The final example of ignition in a practical environment is homogeneous charge, compression ignition (HCCI) which is shown to be a problem dominated by the kinetics intermediate temperature hydrocarbon ignition. Model results show why high hydrocarbon and CO emissions are inevitable in HCCI combustion. The conclusion of this study is that the kinetics of hydrocarbon ignition are actually quite simple, since only one or two elementary reactions are dominant. However, there are many combustion factors that can influence these two major reactions, and these are the features that vary from one practical system to another.

  1. Optimization of metal vapor lasers

    Science.gov (United States)

    Buchanov, V. V.; Molodykh, E. I.; Tykotskii, V. V.

    1983-03-01

    The method proposed here for performing numerical calculations on a computer in order to predict and optimize the characteristics of metal vapor lasers is based on the use of a universal program for numerical experiments designed expressly for metal vapor lasers and on a simultaneous application of an algorithm for multifactor optimization of the output parameters. The latter, in turn, is based on the complex Boks method (Himmelblau, 1970) and on the Gel'fand-Tsetlin ravine method (Himmelblau, 1970). Calculations carried out for a metal with a copper vapor in neon reveal that for optimization with respect to the geometry of the active zone and the parameters of the electrical circuits (including the voltage pulses and excitation frequency) it is sufficient to use the Boks method. The objective function optimum regarding the concentration of the metal particles and the buffer gas found using this algorithm calls for further refinement; this can be performed efficiently with the Gel'fand-Tsetlin ravine method.

  2. 40 CFR 1054.501 - How do I run a valid emission test?

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 32 2010-07-01 2010-07-01 false How do I run a valid emission test... Procedures § 1054.501 How do I run a valid emission test? (a) Applicability. This subpart is addressed to you... your production engines will be equipped with a vapor line that routes running loss vapors into...

  3. AIRFORCE. Aircraft emissions and radiative forcing from emissions

    Energy Technology Data Exchange (ETDEWEB)

    Meijer, E.W.; Kelder, H.; Velthoven, P.F.J. van; Wauben, W.M.F. [Royal Netherlands Meteorological Inst., De Bilt (Netherlands); Beck, J.P.; Velders, G.J.M. [National Inst. of Public Health and the Environment, Bilthoven (Netherlands); Lelieveld, J.; Scheeren, B.A. [Institute of Marine and Atmospheric Research Utrecht (Netherlands)

    1997-12-31

    The Dutch AIRFORCE project focuses on the effects of subsonic aircraft emissions on the chemical composition of the atmosphere and subsequent radiative forcing. It includes measurements in the tropopause region and the modelling of exhaust plumes and large-scale effects. An aircraft exhaust plume model has been developed to study plume processes. The results of the plume model are used in the global transport chemistry model CTMK to determine large-scale effects of plume processes. Due to the efficient conversion of NO{sub x} into HNO{sub 3} inside aircraft exhaust plumes, a decrease of about 25% of the O{sub 3} perturbation was found in the NAFC at 200 hPa in July. Measurements of hydrocarbons revealed a dominant role of the anthropogenic continental emissions of light hydrocarbons in the tropopause region. (author) 20 refs.

  4. Vapor hydrogen and oxygen isotopes reflect water of combustion in the urban atmosphere

    Science.gov (United States)

    Gorski, Galen; Strong, Courtenay; Good, Stephen P.; Bares, Ryan; Ehleringer, James R.; Bowen, Gabriel J.

    2015-01-01

    Anthropogenic modification of the water cycle involves a diversity of processes, many of which have been studied intensively using models and observations. Effective tools for measuring the contribution and fate of combustion-derived water vapor in the atmosphere are lacking, however, and this flux has received relatively little attention. We provide theoretical estimates and a first set of measurements demonstrating that water of combustion is characterized by a distinctive combination of H and O isotope ratios. We show that during periods of relatively low humidity and/or atmospheric stagnation, this isotopic signature can be used to quantify the concentration of water of combustion in the atmospheric boundary layer over Salt Lake City. Combustion-derived vapor concentrations vary between periods of atmospheric stratification and mixing, both on multiday and diurnal timescales, and respond over periods of hours to variations in surface emissions. Our estimates suggest that up to 13% of the boundary layer vapor during the period of study was derived from combustion sources, and both the temporal pattern and magnitude of this contribution were closely reproduced by an independent atmospheric model forced with a fossil fuel emissions data product. Our findings suggest potential for water vapor isotope ratio measurements to be used in conjunction with other tracers to refine the apportionment of urban emissions, and imply that water vapor emissions associated with combustion may be a significant component of the water budget of the urban boundary layer, with potential implications for urban climate, ecohydrology, and photochemistry. PMID:25733906

  5. Vapor hydrogen and oxygen isotopes reflect water of combustion in the urban atmosphere

    Science.gov (United States)

    Gorski, Galen; Strong, Courtenay; Good, Stephen P.; Bares, Ryan; Ehleringer, James R.; Bowen, Gabriel J.

    2015-03-01

    Anthropogenic modification of the water cycle involves a diversity of processes, many of which have been studied intensively using models and observations. Effective tools for measuring the contribution and fate of combustion-derived water vapor in the atmosphere are lacking, however, and this flux has received relatively little attention. We provide theoretical estimates and a first set of measurements demonstrating that water of combustion is characterized by a distinctive combination of H and O isotope ratios. We show that during periods of relatively low humidity and/or atmospheric stagnation, this isotopic signature can be used to quantify the concentration of water of combustion in the atmospheric boundary layer over Salt Lake City. Combustion-derived vapor concentrations vary between periods of atmospheric stratification and mixing, both on multiday and diurnal timescales, and respond over periods of hours to variations in surface emissions. Our estimates suggest that up to 13% of the boundary layer vapor during the period of study was derived from combustion sources, and both the temporal pattern and magnitude of this contribution were closely reproduced by an independent atmospheric model forced with a fossil fuel emissions data product. Our findings suggest potential for water vapor isotope ratio measurements to be used in conjunction with other tracers to refine the apportionment of urban emissions, and imply that water vapor emissions associated with combustion may be a significant component of the water budget of the urban boundary layer, with potential implications for urban climate, ecohydrology, and photochemistry.

  6. Diesel-related hydrocarbons can dominate gas phase reactive carbon in megacities

    Directory of Open Access Journals (Sweden)

    R. E. Dunmore

    2015-09-01

    Full Text Available Hydrocarbons are key precursors to two priority air pollutants, ozone and particulate matter. Those with two to seven carbons have historically been straightforward to observe and have been successfully reduced in many developed cities through air quality policy interventions. Longer chain hydrocarbons released from diesel vehicles are not considered explicitly as part of air quality strategies and there are few direct measurements of their gaseous abundance in the atmosphere. This study describes the chemically comprehensive and continuous measurements of organic compounds in a developed megacity (London, which demonstrate that on a seasonal median basis, diesel-related hydrocarbons represent only 20–30 % of the total hydrocarbon mixing ratio but comprise more than 50 % of the atmospheric hydrocarbon mass and are a dominant local source of secondary organic aerosols. This study shows for the first time that 60 % of the winter primary hydrocarbon hydroxyl radical reactivity is from diesel-related hydrocarbons and using the maximum incremental reactivity scale, we predict that they contribute up to 50 % of the ozone production potential in London. Comparing real-world urban composition with regulatory emissions inventories in the UK and US highlights a previously unaccounted for, but very significant, under-reporting of diesel-related hydrocarbons; an underestimation of a factor ~4 for C9 species rising to a factor of over 70 for C12 during winter. These observations show that hydrocarbons from diesel vehicles can dominate gas phase reactive carbon in cities with high diesel fleet fractions. Future control of urban particulate matter and ozone in such locations requires a shift in policy focus onto gas phase hydrocarbons released from diesels as this vehicle type continues to displace gasoline world-wide.

  7. Thermocatalytic CO2-Free Production of Hydrogen from Hydrocarbon Fuels

    Energy Technology Data Exchange (ETDEWEB)

    University of Central Florida

    2004-01-30

    The main objective of this project is the development of an economically viable thermocatalytic process for production of hydrogen and carbon from natural gas or other hydrocarbon fuels with minimal environmental impact. The three major technical goals of this project are: (1) to accomplish efficient production of hydrogen and carbon via sustainable catalytic decomposition of methane or other hydrocarbons using inexpensive and durable carbon catalysts, (2) to obviate the concurrent production of CO/CO{sub 2} byproducts and drastically reduce CO{sub 2} emissions from the process, and (3) to produce valuable carbon products in order to reduce the cost of hydrogen production The important feature of the process is that the reaction is catalyzed by carbon particulates produced in the process, so no external catalyst is required (except for the start-up operation). This results in the following advantages: (1) no CO/CO{sub 2} byproducts are generated during hydrocarbon decomposition stage, (2) no expensive catalysts are used in the process, (3) several valuable forms of carbon can be produced in the process depending on the process conditions (e.g., turbostratic carbon, pyrolytic graphite, spherical carbon particles, carbon filaments etc.), and (4) CO{sub 2} emissions could be drastically reduced (compared to conventional processes).

  8. Solution deposition of nanometer scale silver films as an alternative to vapor deposition for plasmonic excitation

    Energy Technology Data Exchange (ETDEWEB)

    Smith, Derek S.; Sathish, R. Sai; Kostov, Yordan [Center for Advanced Sensor Technology and Department of Chemical and Biochemical Engineering, University of Maryland Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250 (United States); Rao, Govind, E-mail: grao@umbc.ed [Center for Advanced Sensor Technology and Department of Chemical and Biochemical Engineering, University of Maryland Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250 (United States)

    2010-05-03

    We report the attainment of surface plasmon-coupled emission (SPCE) from highly uniform thin silver films, solution-deposited on glass substrates by a wet chemistry approach. The surface morphology of these films was characterized by atomic force microscopy. The SPCE emission enhancements, polarization and angularity obtained from solution-deposited silver on BK7 glass were comparable to that achieved from conventional SPCE slides prepared via vapor deposition. This facile, wet chemistry procedure for the deposition of SPCE films provides an inexpensive, low maintenance alternative to vapor deposition for SPCE substrate preparation. This would allow the fluorescence observation technique to become more readily available for high sensitivity, low cost applications.

  9. Estimated vapor pressure for WTP process streams

    Energy Technology Data Exchange (ETDEWEB)

    Pike, J. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Poirier, M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2015-01-01

    Design assumptions during the vacuum refill phase of the Pulsed Jet Mixers (PJMs) in the Hanford Waste Treatment and Immobilization Plant (WTP) equate the vapor pressure of all process streams to that of water when calculating the temperature at which the vacuum refill is reduced or eliminated. WTP design authority asked the authors to assess this assumption by performing calculations on proposed feed slurries to calculate the vapor pressure as a function of temperature. The vapor pressure was estimated for each WTP waste group. The vapor pressure suppression caused by dissolved solids is much greater than the increase caused by organic components such that the vapor pressure for all of the waste group compositions is less than that of pure water. The vapor pressure for each group at 145°F ranges from 81% to 98% of the vapor pressure of water. If desired, the PJM could be operated at higher temperatures for waste groups with high dissolved solids that suppress vapor pressure. The SO4 group with the highest vapor pressure suppression could be operated up to 153°F before reaching the same vapor pressure of water at 145°F. However, most groups would reach equivalent vapor pressure at 147 to 148°F. If any of these waste streams are diluted, the vapor pressure can exceed the vapor pressure of water at mass dilution ratios greater than 10, but the overall effect is less than 0.5%.

  10. High Pressure Preignition Chemistry of Hydrocarbons and Hydrocarbon Mixtures

    Science.gov (United States)

    2007-11-02

    and hydrocarbon blends in our various combustion systems, with emphasis on the effects of elevated pressure using our pressurized flow reactor ( PFR ...facility. Detailed experimental data were generated from the PFR for use in associated kinetic modeling work. We continued to develop and extend both

  11. Total Petroleum Hydrocarbons (TPH): ToxFAQs

    Science.gov (United States)

    ... a state: This map displays locations where Total Petroleum Hydrocarbons (TPH) is known to be present. On ... I get more information? ToxFAQs TM for Total Petroleum Hydrocarbons (TPH) ( Hidrocarburos Totales de Petróleo (TPH) ) August ...

  12. Final OSWER Vapor Intrusion Guidance

    Science.gov (United States)

    EPA is preparing to finalize its guidance on assessing and addressing vapor intrusion, which is defined as migration of volatile constituents from contaminated media in the subsurface (soil or groundwater) int