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Sample records for compound nmvoc emissions

  1. Estimation of NMVOC emissions using artificial neural networks and economical and sustainability indicators as inputs.

    PubMed

    Stamenković, Lidija J; Antanasijević, Davor Z; Ristić, Mirjana Đ; Perić-Grujić, Aleksandra A; Pocajt, Viktor V

    2016-06-01

    This paper describes the development of an artificial neural network (ANN) model based on economical and sustainability indicators for the prediction of annual non-methane volatile organic compounds (NMVOCs) emissions in China for the period 2005-2011 and its comparison with inventory emission factor models. The NMVOCs emissions in China were estimated using ANN model which was created using available data for nine European countries, which NMVOC emission per capita approximately correspond to the Chinese emissions, for the period 2004-2012. The forward input selection strategy was used to compare the significance of particular inputs for the prediction of NMVOC emissions in the nine selected EU countries and China. The final ANN model was trained using only five input variables, and it has demonstrated similar accuracy in predicting NMVOC emissions for the selected EU countries that were used for the development of the model and then for China for which the input dataset was previously unknown to the ANN model. The obtained mean absolute percentage error (MAPE) values were 8 % for EU countries and 5 % for China. Also, the temporal trend of NMVOC emissions predicted in this study is generally consistent with the trend obtained using inventory emission models. The proposed ANN approach can represent a viable alternative for the prediction of NMVOC emissions at the national level, in particular for developing countries which are usually lacking emission data.

  2. Indian emissions of technology-linked NMVOCs with chemical speciation: An evaluation of the SAPRC99 mechanism with WRF-CAMx simulations

    NASA Astrophysics Data System (ADS)

    Sarkar, M.; Venkataraman, C.; Guttikunda, S.; Sadavarte, P.

    2016-06-01

    Non-methane volatile organic compounds (NMVOCs) are important precursors to reactions producing tropospheric ozone and secondary organic aerosols. The present work uses a detailed technology-linked NMVOC emission database for India, along with a standard mapping method to measured NMVOC profiles, to develop speciated NMVOC emissions, which are aggregated into multiple chemical mechanisms used in chemical transport models. The fully speciated NMVOC emissions inventory with 423 constituent species, was regrouped into model-ready reactivity classes of the RADM2, SAPRC99 and CB-IV chemical mechanisms, and spatially distributed at 25 × 25 km2 resolution, using source-specific spatial proxies. Emissions were considered from four major sectors, i.e. industry, transport, agriculture and residential and from non-combustion activities (use of solvents and paints). It was found that residential cooking with biomass fuels, followed by agricultural residue burning in fields and on-road transport, were largest contributors to the highest reactivity group of NMVOC emissions from India. The emissions were evaluated using WRF-CAMx simulations, using the SAPRC99 photochemical mechanism, over India for contrasting months of April, July and October 2010. Modelled columnar abundance of NO2, CO and O3 agreed well with satellite observations both in magnitude and spatial distribution, in the three contrasting months. Evaluation of monthly and spatial differences between model predictions and observations indicates the need for further refinement of the spatial distribution of NOX emissions, spatio-temporal distribution of agricultural residue burning emissions.

  3. Improved sectoral allocation of NMVOC emissions from solvent use in Greece.

    PubMed

    Sidiropoulos, Christos; Tsilingiridis, George

    2009-06-15

    Solvent use and road transport are the two most significant sources of NMVOC emissions in urban environments. The allocation of emissions to solvent-related activities is of major importance since it is a major step towards providing spatially and temporally resolved accurate emission data in air quality models and assisting the development of properly orientated emission reduction measures. In this paper an activity-specific NMVOC emission inventory from solvent use in Greece is presented. The diversity, the volume and the complexity of the relevant activity data and, in some cases, the use of the same solvent and/or product in a variety of uses are the main difficulties in solvent emission inventorying. To overcome them, an extensive market research/survey is performed, combined with a literature review and expert opinion, to determine solvent utilization factors (expressed via usage factors as solvents, or per activity and/or per process). With the aid of these usage factors, appropriate emission factors, national statistical activity data and the calculating formulas developed, emissions are estimated and attributed to each solvent-related activity. Main results indicate that the use of solvents is the second source of NMVOC emissions in Greece (72+/-4 kt in 2003), the road transport sector being the first one (171 kt). Paint applications are the most important source of solvent NMVOC emissions, accounting for 44.5+/-2.5% of the total solvent NMVOC followed by the domestic use of solvents (excluding paint), which accounts for 39+/-2% of total solvent NMVOC.

  4. NMVOCs speciated emissions from mobile sources and their effect on air quality and human health in the metropolitan area of Buenos Aires, Argentina

    NASA Astrophysics Data System (ADS)

    D'Angiola, Ariela; Dawidowski, Laura; Gomez, Dario; Granier, Claire

    2014-05-01

    Since 2007, more than half of the world's population live in urban areas. Urban atmospheres are dominated by pollutants associated with vehicular emissions. Transport emissions are an important source of non-methane volatile organic compounds (NMVOCs) emissions, species of high interest because of their negative health effects and their contribution to the formation of secondary pollutants responsible for photochemical smog. NMVOCs emissions are generally not very well represented in emission inventories and their speciation presents a high level of uncertainty. In general, emissions from South American countries are still quite unknown for the international community, and usually present a high degree of uncertainty due to the lack of available data to compile emission inventories. Within the Inter-American Institute for Global Change Research (IAI, www.iai.int) projects, UMESAM (Urban Mobile Emissions in South American Megacities) and SAEMC (South American Emissions, Megacities and Climate, http://saemc.cmm.uchile.cl/), the effort was made to compute on-road transport emission inventories for South American megacities, namely Bogota, Buenos Aires, Lima, Sao Paulo and Santiago de Chile, considering megacities as urban agglomerations with more than 5 million inhabitants. The present work is a continuation of these projects, with the aim to extend the calculated NMVOCs emissions inventory into the individual species required by CTMs. The on-road mobile sector of the metropolitan area of Buenos Aires (MABA), Argentina, accounted for 70 Gg of NMVOCs emissions for 2006, without considering two-wheelers. Gasoline light-duty vehicles were responsible for 64% of NMVOCs emissions, followed by compressed natural gas (CNG) light-duty vehicles (22%), diesel heavy-duty vehicles (11%) and diesel light-duty vehicles (7%). NMVOCs emissions were speciated according to fuel and technology, employing the European COPERT (Ntziachristos & Samaras, 2000) VOCs speciation scheme for

  5. On-road measurements of NMVOCs and NOx: Determination of light-duty vehicles emission factors from tunnel studies in Brussels city center

    NASA Astrophysics Data System (ADS)

    Ait-Helal, W.; Beeldens, A.; Boonen, E.; Borbon, A.; Boréave, A.; Cazaunau, M.; Chen, H.; Daële, V.; Dupart, Y.; Gaimoz, C.; Gallus, M.; George, C.; Grand, N.; Grosselin, B.; Herrmann, H.; Ifang, S.; Kurtenbach, R.; Maille, M.; Marjanovic, I.; Mellouki, A.; Miet, K.; Mothes, F.; Poulain, L.; Rabe, R.; Zapf, P.; Kleffmann, J.; Doussin, J.-F.

    2015-12-01

    Emission factors (EFs) of pollutants emitted by light-duty vehicles (LDV) were investigated in the Leopold II tunnel in Brussels city center (Belgium), in September 2011 and in January 2013, respectively. Two sampling sites were housing the instruments for the measurements of a large range of air pollutants, including non-methane volatile organic compounds (NMVOCs), nitrogen oxides (NOx) and carbon dioxide (CO2). The NMVOCs and NOx traffic EFs for LDV were determined from their correlation with CO2 using a single point analysis method. The emission factor of NOx is (544 ± 199) mg vehicle-1 km-1; NMVOCs emission factors vary from (0.26 ± 0.09) mg vehicle-1 km-1 for cis-but-2-ene to (8.11 ± 2.71) mg vehicle-1 km-1 for toluene. Good agreement is observed between the EFs determined in the Leopold II tunnel and the most recent EFs determined in another European roadway tunnel in 2004, with only a slight decrease of the EFs during the last decade. An historical perspective is provided and the observed trend in the NMVOCs emission factors reflect changes in the car fleet composition, the fuels and/or the engine technology that have occurred within the last three decades in Europe.

  6. Coincident Observations of Surface Ozone and NMVOCs over Abu Dhabi

    NASA Astrophysics Data System (ADS)

    Abbasi, Naveed; Majeed, Tariq; Iqbal, Mazhar; Tarasick, David; Davies, Jonathan; Riemer, Daniel; Apel, Eric

    2016-07-01

    The vertical profiles of ozone are measured coincidently with non-methane volatile organic compounds (NMVOCs) at the meteorological site located at the Abu Dhabi international airport (latitude 24.45N; longitude 54.22E) during the years 2012 - 2014. Some of the profiles show elevated surface ozone >95 ppbv during the winter months (December, January and February). The ground-level NMVOCs obtained from the gas chromatography-flame ionization detection/mass spectrometry system also show elevated values of acetylene, ethane, propane, butane, pentane, benzene, and toluene. NMVOCs and ozone abundances in other seasons are much lower than the values in winter season. NMVOCs are emitted from an extensive number of sources in urban environments including fuel production, distribution, and consumption, and serve as precursor of ozone. Transport sources contribute a substantial portion of the NMVOC burden to the urban atmosphere in developed regions. Abu Dhabi is located at the edge of the Arabian Gulf and is highly affected by emissions from petrochemical industries in the neighboring Gulf region. The preliminary results indicate that wintertime enhancement in ozone is associated with large values of NMVOCs at Abu Dhabi. The domestic production of surface ozone is estimated from the combination of oxygen recombination and NMVOCs and compared with the data. It is estimated that about 40-50% of ozone in Abu Dhabi is transported from the neighbouring petrochemical industries. We will present ozone sounding and NMVOCs data and our model estimates of surface ozone, including a discussion on the high levels of the tropospheric ozone responsible for contaminating the air quality in the UAE. This work is supported by National Research Foundation, UAE.

  7. Net radiative forcing responses to regional CO and NMVOC reductions

    NASA Astrophysics Data System (ADS)

    Fry, M. M.; Schwarzkopf, M. D.; Adelman, Z.; Naik, V.; West, J.

    2012-12-01

    Recent studies suggest that short-lived pollutants and their precursors be considered in near-term climate mitigation strategies, in addition to national air quality programs, but their associated forcings vary based on the region of emissions. Here we quantify the net radiative forcing (RF) impacts of regional anthropogenic carbon monoxide (CO) and non-methane volatile organic compound (NMVOC) emissions due to changes in the tropospheric concentrations of ozone (O3), methane (CH4), and aerosols (carbonaceous and sulfate), to inform future coordinated actions addressing air quality and climate forcing. We present the RF from CO and NMVOC emission reductions from 10 regions (North America, South America, Europe, Former Soviet Union, Southern Africa, India, East Asia, Southeast Asia, Australia and New Zealand, and Middle East and Northern Africa). The global chemical transport model MOZART-4 is used to simulate tropospheric concentration changes, using the IPCC AR5 Representative Concentration Pathway 8.5 (RCP 8.5) emissions inventory for 2005 and global meteorology from the Goddard Earth Observing System Model, version 5 (GEOS-5) for the years 2004-2005. We utilize the NOAA Geophysical Fluid Dynamics Laboratory standalone radiative transfer model to calculate the stratospheric-adjusted net RF for each regional CO and NMVOC reduction, relative to the base. We find that global annual net RF per unit change in emissions ranges from -0.115 to -0.131 mW m-2 / Tg CO for CO reductions, and -0.0035 to -0.436 mW m-2 / Tg C for NMVOC reductions, with the regions in the tropics providing the greatest improvements (Middle East, Southeast Asia, and India CO reductions, and Middle East, Africa, and India NMVOC reductions). The net RF distributions for the CO and NMVOC reductions show widespread cooling across the northern and southern hemispheres corresponding to the patterns of O3 and CH4 decreases, and localized positive and negative net RFs due to increases and decreases in

  8. Variation of the NMVOC speciation in the solvent sector and the sensitivity of modelled tropospheric ozone

    NASA Astrophysics Data System (ADS)

    von Schneidemesser, E.; Coates, J.; Denier van der Gon, H. A. C.; Visschedijk, A. J. H.; Butler, T. M.

    2016-06-01

    Non-methane volatile organic compounds (NMVOCs) are detrimental to human health owing to the toxicity of many of the NMVOC species, as well as their role in the formation of secondary air pollutants such as tropospheric ozone (O3) and secondary organic aerosol. The speciation and amount of NMVOCs emitted into the troposphere are represented in emission inventories (EIs) for input to chemical transport models that predict air pollutant levels. Much of the information in EIs pertaining to speciation of NMVOCs is likely outdated, but before taking on the task of providing an up-to-date and highly speciated EI, a better understanding of the sensitivity of models to the change in NMVOC input would be highly beneficial. According to the EIs, the solvent sector is the most important sector for NMVOC emissions. Here, the sensitivity of modelled tropospheric O3 to NMVOC emission inventory speciation was investigated by comparing the maximum potential difference in O3 produced using a variety of reported solvent sector EI speciations in an idealized study using a box model. The sensitivity was tested using three chemical mechanisms that describe O3 production chemistry, typically employed for different types of modelling scales - point (MCM v3.2), regional (RADM2), and global (MOZART-4). In the box model simulations, a maximum difference of 15 ppbv (ca. 22% of the mean O3 mixing ratio of 69 ppbv) between the different EI speciations of the solvent sector was calculated. In comparison, for the same EI speciation, but comparing the three different mechanisms, a maximum difference of 6.7 ppbv was observed. Relationships were found between the relative contribution of NMVOC compound classes (alkanes and oxygenated species) in the speciations to the amount of Ox produced in the box model. These results indicate that modelled tropospheric O3 is sensitive to the speciation of NMVOCs as specified by emission inventories, suggesting that detailed updates to the EI speciation

  9. Characterizing reduced sulfur compounds and non-methane volatile organic compounds emissions from a swine concentrated animal feeding operation

    NASA Astrophysics Data System (ADS)

    Rumsey, Ian Cooper

    Reduced sulfur compounds (RSCs) and non-methane volatile organic compounds (NMVOCs) emissions from concentrated animal feeding operations (CAFOs) have become a potential environmental and human health concern. Both RSCs and NMVOCs contribute to odor. In addition, RSCs also have the potential to form fine particulate matter (PMfine) and NMVOCs the potential to form ozone. Measurements of RSCs and NMVOCs emissions were made from both an anaerobic lagoon and barn at a swine CAFO in North Carolina. Emission measurements were made over all four seasonal periods. In each seasonal period, measurements were made from both the anaerobic lagoon and barn for ˜1 week. RSC and NMVOCs samples were collected using passivated canisters. Nine to eleven canister samples were taken from both the lagoon and barn over each sampling period. The canisters were analyzed ex-situ using gas chromatography flame ionization detection (GC-FID). Hydrogen sulfide (H2S) measurements were made in-situ using a pulsed fluorescence H2S/SO2 analyzer. During sampling, measurements of meteorological and physiochemical parameters were made. H2S had the largest RSC flux, with an overall average lagoon flux of 1.33 mug m-2 min-1. The two main RSCs identified by the GC-FID, dimethyl sulfide (DMS) and dimethyl disulfide (DMDS), had overall average lagoon fluxes an order of magnitude lower, 0.12 and 0.09 mug m-2 min-1, respectively. Twelve significant NMVOCs were identified in lagoon samples (ethanol, 2-ethyl-1-hexanol, methanol, acetaldehyde, decanal, heptanal, hexanal, nonanal, octanal, acetone, methyl ethyl ketone, and 4-methylphenol). The overall average fluxes for these NMVOCs, ranged from 0.08 mug m-2 min-1 (4-methylphenol) to 2.11 mug m-2 min-1 (acetone). Seasonal H2S barn concentrations ranged from 72-631 ppb. DMS and DMDS seasonal concentrations were 2-3 orders of magnitude lower. There were six significant NMVOCs identified in barn samples (methanol, ethanol, acetone 2-3 butanedione, acetaldehyde

  10. Characterizing Non-Methane Volatile Organic Compounds Emissions from a Swine Concentrated Animal Feeding Operation

    NASA Astrophysics Data System (ADS)

    Aneja, V. P.; Rumsey, I. C.; Lonneman, W. A.

    2011-12-01

    The emission of NMVOCs from swine concentrated animal feeding operations (CAFOs) in North Carolina is of concern, due to their contribution to odor. In addition, of the 188 listed hazardous air pollutants (HAPs), 162 are classified as NMVOCs. NMVOCs emissions were determined over four seasonal sampling periods from an anaerobic lagoon and barn at a swine CAFO in North Carolina. Sampling was conducted during the period June 2007 through April 2008. Air samples were collected using SUMMA and fused-silca lined (FSL) canisters and were analyzed for NMVOCs using a gas chromatography flame ionization detection (GC-FID) system. Nine to eleven canister samples were collected from both the anaerobic lagoon and the barn over a ~1 week sampling period, with samples collected on a minimum of four different days. Measurements of meteorological and physiochemical parameters were made during the lagoon and barn sampling. Six NMVOCs (acetone, acetaldehyde, ethanol, 2-ethyl-1-hexanol, methanol and methyl ethyl ketone (MEK)) were identified in lagoon samples, that were classified as having significantly larger emissions in comparison to other NMVOCs. Overall average lagoon fluxes of these NMVOCs ranged from 0.18 ug m-2 min-1 for 2-ethyl-1-hexanol to 2.11 ug m-2 min-1 for acetone. In barn samples there were also six NMVOCs (acetaldehyde, acetone, 2,3-butanedione, ethanol, methanol and 4-methylphenol) that were classified as having significantly larger emissions in comparison to other compounds. Overall average concentrations for these six compounds ranged from 2.87 ppb for 4-methylphenol to 16.12 ppb for ethanol. The overall average normalized emissions ranged from 0.10 g day-1 AU-1 (AU = one animal unit, representing 500 kg of live animal weight) for acetaldehyde to 0.45 g day-1 AU-1 for ethanol. Eight odorous compounds were identified in lagoon and barn samples. These were 2,3-butanedione, decanal, ethylbenzene, heptanal, hexanal, 4-methylphenol, nonanal, and octanal. Of the eight

  11. Characterizing non-methane volatile organic compounds emissions from a swine concentrated animal feeding operation

    NASA Astrophysics Data System (ADS)

    Rumsey, Ian C.; Aneja, Viney P.; Lonneman, William A.

    2012-02-01

    Emissions of non-methane volatile organic compounds (NMVOCs) were determined from a swine concentrated animal feeding operation (CAFO) in North Carolina. NMVOCs were measured in air samples collected in SUMMA and fused-silica lined (FSL) canisters and were analyzed using a gas chromatography flame ionization detection (GC-FID) system. Measurements were made from both an anaerobic lagoon and barn in each of the four seasonal sampling periods during the period June 2007 through April 2008. In each sampling period, nine to eleven canister samples were taken from both the anaerobic lagoon and barn over a minimum of four different days during a period of ˜1 week. Measurements of meteorological and physiochemical parameters were also made during the sampling period. In lagoon samples, six NMVOCs were identified that had significantly larger emissions in comparison to other NMVOCs. This included three alcohols (ethanol, 2-ethyl-1-hexanol, and methanol), two ketones (acetone and methyl ethyl ketone (MEK)) and an aldehyde (acetaldehyde). The overall average fluxes for these NMVOCs, ranged from 0.18 μg m -2 min -1 for 2-ethyl-1-hexanol to 2.11 μg m -2 min -1 for acetone, with seasonal fluxes highest in the summer for four (acetone, acetaldehyde, 2-ethyl-1-hexanol and MEK) of the six compounds In barn samples, there were six NMVOCs that had significantly larger concentrations and emissions in comparison to other NMVOCs. These consisted of two alcohols (methanol and ethanol), an aldehyde (acetaldehyde), two ketones (acetone and 2,3-butanedione), and a phenol (4-methylphenol). Overall average barn concentration ranged from 2.87 ppb for 4-methylphenol to 16.12 ppb for ethanol. Overall average normalized barn emission rates ranged from 0.10 g day -1 AU -1 (1 AU (animal unit) = 500 kg of live animal weight) for acetaldehyde to 0.45 g day -1 AU -1 for ethanol. The NMVOCs, 4-methylphenol and 2,3-butanedione, which have low odor thresholds (odor thresholds = 1.86 ppb and 0

  12. Intraannual cycles of NMVOCs in the tropical troposphere and their use for interpreting seasonal variability in CO

    NASA Astrophysics Data System (ADS)

    Read, K.; Carpenter, L.; Lewis, A.; Lee, J.; Neves, L.; Faria, B.

    2009-04-01

    18 month's data of non-methane volatile organic compound (NMVOC) and carbon monoxide (CO) concentrations obtained from the Cape Verde Atmospheric Observatory (Observatório Atmosferico de Cabo Verde: Humberto Duarte Fonseca CVAO, 16,848°N, 24.871°W) in the tropical Atlantic Ocean are presented here. The CO measurements demonstrate the expected sinusoidal curve driven by its loss reaction with OH, but with a smaller amplitude than modelling studies would suggest for this region. Simultaneous ethane measurements were used to derive the seasonal variation in the "nominal hydroxyl radical (OH) concentration (n[OH])" experienced along the air mass trajectory of ethane, by assuming a fixed ethane emission rate. The n[OH] represents the variability in OH concentration assuming there are no intraannual changes in ethane emissions, and was subsequently used to create seasonal fits of CO concentrations, allowing interpretation of differing sources and sinks from those of ethane. Deviation of the measured CO concentrations from their "n[OH] fit" indicates that summer sources of CO are approximately 60% higher than winter, assuming that ethane is not lost through reactions with chlorine or bromine atoms. Evidence suggests that the production of CO from the oxidation of CH4 and NMVOC and in particular from methanol, acetone and acetaldehyde (from both terrestrial and oceanic sources) is increased in this region in summer and this could be an explanation for the observations. Other NMVOC measurements are presented here as indicators of potential conflicting halogen chemistry and of alternative emission sources. Longer-term measurements of NMVOC and CO, such as those presented in this paper, are essential for our understanding of the oxidation capacity, atmospheric processes and composition of the atmosphere.

  13. Emission, speciation, and evaluation of impacts of non-methane volatile organic compounds from open dump site.

    PubMed

    Majumdar, Dipanjali; Ray, Sandipan; Chakraborty, Sucharita; Rao, Padma S; Akolkar, A B; Chowdhury, M; Srivastava, Anjali

    2014-07-01

    Surface emission from Dhapa, the only garbage disposal ground in Kolkata, is a matter of concern to the local environment and also fuels the issues of occupational and environmental health. Surface emission of the Dhapa landfill site was studied using a flux chamber measurement for nonmethane volatile organic compounds (NMVOCs). Eighteen noncarbonyl volatile organic compounds (VOCs) and 14 carbonyl VOCs, including suspected and known carcinogens, were found in appreciable concentrations. The concentrations of the target species in the flux chamber were found to be significantly higher for most of the species in summer than winter. Surface emission rate of landfill gas was estimated by using two different approaches to assess the applicability for an open landfill site. It was found that the emissions predicted using the model Land GEM version 3.02 is one to two orders less than the emission rate calculated from flux chamber measurement for the target species. Tropospheric ozone formation has a serious impact for NMVOC emission. The total ozone-forming potential (OFP) of the Dhapa dumping ground considering all target NMVOCs was estimated to be 4.9E+04 and 1.2E+05 g/day in winter and summer, respectively. Also, it was found that carbonyl VOCs play a more important role than noncarbonyl VOCs for tropospheric ozone formation. Cumulative cancer risk estimated for all the carcinogenic species was found to be 2792 for 1 million population, while the total noncancer hazard index (HI) was estimated to be 246 for the occupational exposure to different compounds from surface emission to the dump-site workers at Dhapa. Implications: This paper describes the real-time surface emission of NMVOCs from an open municipal solid waste (MSW) dump site studied using a flux chamber. Our study findings indicate that while planning for new landfill site in tropical meteorology, real-time emission data must be considered, rather than relying on modeled data. The formation of tropospheric

  14. Estimating the biogenic emissions of non-methane volatile organic compounds from the North Western Mediterranean vegetation of Catalonia, Spain.

    PubMed

    Parra, R; Gassó, S; Baldasano, J M

    2004-08-15

    An estimation of the magnitude of non-methane volatile organic compounds (NMVOCs) emitted by vegetation in Catalonia (NE of the Iberian Peninsula, Spain), in addition to their superficial and temporal distribution, is presented for policy and scientific (photochemical modelling) purposes. It was developed for the year 2000, for different time resolutions (hourly, daily, monthly and annual) and using a high-resolution land-use map (1-km2 squared cells). Several meteorological surface stations provided air temperature and solar radiation data. An adjusted mathematical emission model taking account of Catalonia's conditions was built into a geographic information system (GIS) software. This estimation uses the latest information, mainly relating to: (1) emission factors; (2) better knowledge of the composition of Catalonia's forest cover; and (3) better knowledge of the particular emission behaviour of some Mediterranean vegetal species. Results depict an annual cycle with increasing values in the March-April period with the highest emissions in July-August, followed by a decrease in October-November. Annual biogenic NMVOCs emissions reach 46.9 kt, with monoterpenes the most abundant species (24.7 kt), followed by other biogenic volatile organic compounds (e.g. alcohols, aldehydes and acetone) (16.3 kt), and isoprene (5.9 kt). These compounds signify 52%, 35% and 13%, respectively, of total emission estimates. Peak hourly total emission for a winter day could be less than 10% of the corresponding value for a summer day.

  15. Non-methane volatile organic compound flux from a subarctic mire in Northern Sweden

    NASA Astrophysics Data System (ADS)

    Bäckstrand, Kristina; Crill, Patrick M.; Mastepanov, Mikhail; Christensen, Torben R.; Bastviken, David

    2008-04-01

    Biogenic NMVOCs are mainly formed by plants and microorganisms. They have strong impact on the local atmospheric chemistry when emitted to the atmosphere. The objective of this study was to determine if there are significant emissions of non-methane volatile organic compounds (NMVOCs) from a subarctic mire in northern Sweden. Subarctic peatlands in discontinuous permafrost regions are undergoing substantial environmental changes due to their high sensitivity to climate warming and there is need for including NMVOCs in the overall carbon budget. Automatic and manual chamber measurements were used to estimate NMVOC fluxes from three dominating subhabitats on the mire during three growing seasons. Emission rates varied and were related to plant species distribution and seasonal net ecosystem exchange of carbon dioxide. The highest fluxes were observed from wetter sites dominated by Eriophorum and Sphagnum spp. Total NMVOC emissions from the mire (~17 ha) is estimated to consist of ~150 kgC during a growing season with 150 d. NMVOC fluxes can account for ~5% of total net carbon exchange (-3177 kgC) at the mire during the same period. NMVOC emissions are therefore a significant component in a local carbon budget for peatlands.

  16. The biogenic volatile organic compounds emission inventory in France: application to plant ecosystems in the Berre-Marseilles area (France).

    PubMed

    Simon, Valérie; Dumergues, Laurent; Ponche, Jean-Luc; Torres, Liberto

    2006-12-15

    An inventory describing the fluxes of volatile organic compounds (VOCs), isoprene and monoterpenes, and other VOCs (OVOCs) from the biosphere to the atmosphere, has been constructed within the framework of the ESCOMPTE project (fiEld experimentS to COnstrain Models of atmospheric Pollution and Transport of Emissions). The area concerned, located around Berre-Marseilles, is a Mediterranean region frequently subject to high ozone concentrations. The inventory has been developed using a fine scale land use database for the year 1999, forest composition statistics, emission potentials from individual plant species, biomass distribution, temperature and light intensity. The seasonal variations in emission potentials and biomass were also taken into account. Hourly meteorological data for 1999 were calculated from ALADIN data and these were used to predict the hourly isoprene, monoterpene and OVOC fluxes for the area on a 1 kmx1 km spatial grid. Estimates of annual biogenic isoprene, monoterpene and OVOC fluxes for the reference year 1999 were 20.6, 38.9 and 13.3 kt, respectively, Quercus pubescens, Quercus ilex, Pinus halepensis and garrigue vegetation are the dominant emitting species of the area. VOC emissions from vegetation in this region contribute approximately 94% to the NMVOC (non-methane volatile organic compounds) of natural origin and are of the same order of magnitude as NMVOC emissions from anthropogenic sources. These results complete the global ESCOMPTE database needed to make an efficient strategy for tropospheric ozone reduction policy.

  17. Laboratory measurements of emission factors of nonmethane volatile organic compounds from burning of Chinese crop residues

    NASA Astrophysics Data System (ADS)

    Inomata, Satoshi; Tanimoto, Hiroshi; Pan, Xiaole; Taketani, Fumikazu; Komazaki, Yuichi; Miyakawa, Takuma; Kanaya, Yugo; Wang, Zifa

    2015-05-01

    The emission factors (EFs) of nonmethane volatile organic compounds (NMVOCs) emitted during the burning of Chinese crop residue were investigated as a function of modified combustion efficiency in laboratory experiments. NMVOCs, including acetonitrile, aldehydes/ketones, furan, and aromatic hydrocarbons, were monitored by proton-transfer-reaction mass spectrometry. Rape plant was burned in dry conditions and wheat straw was burned in both wet and dry conditions to simulate the possible burning of damp crop residue in regions of high temperature and humidity. We compared the present data to field data reported by Kudo et al. (2014). Good agreement between field and laboratory data was obtained for aromatics under relatively more smoldering combustion of dry samples, but laboratory data were slightly overestimated compared to field data for oxygenated VOC (OVOC). When EFs from the burning of wet samples were investigated, the consistency between the field and laboratory data for OVOCs was stronger than for dry samples. This may be caused by residual moisture in crop residue that has been stockpiled in humid regions. Comparison of the wet laboratory data with field data suggests that Kudo et al. (2014) observed the biomass burning plumes under relatively more smoldering conditions in which approximately a few tens of percentages of burned fuel materials were wet.

  18. Compilation and analyses of emissions inventories for the NOAA atmospheric chemistry project. Progress report, August 1997

    SciTech Connect

    Benkovitz, C.M.

    1997-09-01

    Global inventories of anthropogenic emissions of oxides of nitrogen for circa 1985 and 1990 and non-methane volatile organic compounds (NMVOCs) for circa 1990 have been compiled by this project. Work on the inventories has been carried out under the umbrella of the Global Emissions Inventory Activity of the International Global Atmospheric Chemistry program. Global emissions of NOx for 1985 are estimated to be 21 Tg N/yr, with approximately 84% originating in the Northern Hemisphere. The global emissions for 1990 are 31 Tg N/yr for NOx and 173 Gg NMVOC/yr. Ongoing research activities for this project continue to address emissions of both NOx and NMVOCs. Future tasks include: evaluation of more detailed regional emissions estimates and update of the default 1990 inventories with the appropriate estimates; derivation of quantitative uncertainty estimates for the emission values; and development of emissions estimates for 1995.

  19. Intra-annual cycles of NMVOC in the tropical marine boundary layer and their use for interpreting seasonal variability in CO

    NASA Astrophysics Data System (ADS)

    Read, K. A.; Lee, J. D.; Lewis, A. C.; Moller, S. J.; Mendes, L.; Carpenter, L. J.

    2009-11-01

    Carbon monoxide and nonmethane volatile organic compounds (NMVOC) have been measured for the first time on a continuous basis in the tropical marine boundary layer of the Atlantic Ocean. CO and ethane, which have similar lifetimes with respect to OH degradation, vary intra-annually with the sinusoidal variability expected due to a primary hydroxyl radical (OH) sink, but with CO showing a smaller cycle amplitude. The ethane measurements were used to derive the seasonal variation in the nominal OH concentration (n[OH]) experienced along the air mass trajectories arriving at Cape Verde. The n[OH] represents the variability in both the true OH concentration and any intra-annual changes in ethane emissions, and was subsequently used to simulate the seasonal cycle of CO, allowing identification of potentially differing sources and sinks from those of ethane. Deviation of the observed CO from the n[OH] fit indicated that summer sources of CO are approximately 60% (30-68%) higher than winter, assuming values of ±8% and ±49% seasonal variability, respectively, in fossil fuel and biomass burning emissions of CO and ethane, and including -29% uncertainty due to the losses of ethane through reaction with chlorine atoms. The evidence suggests that secondary production of CO from the oxidation of methane (CH4) and NMVOC and in particular from methanol, acetone and acetaldehyde may be dominant summer CO sources in this region.

  20. Volatile organic compound emissions from silage systems

    Technology Transfer Automated Retrieval System (TEKTRAN)

    As a precursor to smog, emission of volatile organic compounds (VOCs) to the atmosphere is an environmental concern in some regions. The major source from farms is silage, with emissions coming from the silo face, mixing wagon, and feed bunk. The major compounds emitted are alcohols with other impor...

  1. Complex fragment emission from hot compound nuclei

    SciTech Connect

    Moretto, L.G.

    1986-03-01

    The experimental evidence for compound nucleus emission of complex fragments at low energies is used to interpret the emission of the same fragments at higher energies. The resulting experimental picture is that of highly excited compound nuclei formed in incomplete fusion processes which decay statistically. In particular, complex fragments appear to be produced mostly through compound nucleus decay. In the appendix a geometric-kinematic theory for incomplete fusion and the associated momentum transfer is outlined. 10 refs., 19 figs.

  2. Emission trends and mitigation options for air pollutants in East Asia

    NASA Astrophysics Data System (ADS)

    Wang, S. X.; Zhao, B.; Cai, S. Y.; Klimont, Z.; Nielsen, C. P.; Morikawa, T.; Woo, J. H.; Kim, Y.; Fu, X.; Xu, J. Y.; Hao, J. M.; He, K. B.

    2014-07-01

    Emissions of air pollutants in East Asia play an important role in the regional and global atmospheric environment. In this study we evaluated the recent emission trends of sulfur dioxide (SO2), nitrogen oxides (NOx), particulate matter (PM), and non-methane volatile organic compounds (NMVOC) in East Asia, and projected their future emissions up until 2030 with six emission scenarios. The results will provide future emission projections for the modeling community of the model inter-comparison program for Asia (MICS-Asia). During 2005-2010, the emissions of SO2 and PM2.5 in East Asia decreased by 15 and 12%, respectively, mainly attributable to the large-scale deployment of flue gas desulfurization (FGD) at China's power plants, and the promotion of highly efficient PM removal technologies in China's power plants and cement industry. During this period, the emissions of NOx and NMVOC increased by 25 and 15%, driven by rapid increase in the emissions from China due to inadequate control strategies. In contrast, the NOx and NMVOC emissions in East Asia except China decreased by 13-17%, mainly due to the implementation of stringent vehicle emission standards in Japan and South Korea. Under current regulations and current levels of implementation, NOx, SO2, and NMVOC emissions in East Asia are projected to increase by about one-quarter over 2010 levels by 2030, while PM2.5 emissions are expected to decrease by 7%. Assuming enforcement of new energy-saving policies, emissions of NOx, SO2, PM2.5 and NMVOC in East Asia are expected to decrease by 28, 36, 28, and 15%, respectively, compared with the baseline case. The implementation of "progressive" end-of-pipe control measures would lead to another one-third reduction of the baseline emissions of NOx, and about one-quarter reduction of SO2, PM2.5, and NMVOC. Assuming the full application of technically feasible energy-saving policies and end-of-pipe control technologies, the emissions of NOx, SO2, and PM2.5 in East Asia

  3. Emission trends and mitigation options for air pollutants in East Asia

    NASA Astrophysics Data System (ADS)

    Wang, S. X.; Zhao, B.; Cai, S. Y.; Klimont, Z.; Nielsen, C.; McElroy, M. B.; Morikawa, T.; Woo, J. H.; Kim, Y.; Fu, X.; Xu, J. Y.; Hao, J. M.; He, K. B.

    2014-01-01

    Emissions of air pollutants in East Asia play an important role in the regional and global atmospheric environment. In this study we evaluated the recent emission trends of sulfur dioxide (SO2), nitrogen oxides (NOx), particulate matters (PM), and non-methane volatile organic compounds (NMVOC) in East Asia, and projected their future emissions up to 2030 with six emission scenarios. The results will provide future emission projections for the modeling community of the model inter-comparison program for Asia (MICS-Asia). During 2005-2010, the emissions of SO2 and PM2.5 in East Asia decreased by 15 % and 11%, respectively, mainly attributable to the large scale deployment of FGD for China's power plants, and the promotion of high-efficient PM removal technologies in China's power plants and cement industry. During this period, the emissions of NOx and NMVOC increased by 25% and 15%, driven by the rapid increase in the emissions from China owing to inadequate control strategies. In contrast, the NOx and NMVOC emissions in East Asia except China decreased by 13-17% mainly due to the implementation of tight vehicle emission standards in Japan and South Korea. Under current legislation and current implementation status, NOx, SO2, and NMVOC emissions in East Asia are estimated to increase by about one quarter by 2030 from the 2010 levels, while PM2.5 emissions are expected to decrease by 7%. Assuming enforcement of new energy-saving policies, emissions of NOx, SO2, PM2.5 and NMVOC in East Asia are expected to decrease by 28%, 36%, 28%, and 15% respectively compared with the baseline case. The implementation of the "progressive" end-of-pipe control measures is expected to lead to another one third reduction of the baseline emissions of NOx, and about one quarter reduction for SO2, PM2.5, and NMVOC. With the full implementation of maximum feasible reduction measures, the emissions of NOx, SO2, and PM2.5 in East Asia are expected to account for only about one quarter and

  4. COMPILATION AND ANALYSES OF EMISSIONS INVENTORIES FOR THE NOAA ATMOSPHERIC CHEMISTRY PROJECT. PROGRESS REPORT, AUGUST 1997.

    SciTech Connect

    BENKOVITZ,C.M.

    1997-09-01

    Global inventories of anthropogenic emissions of oxides of nitrogen (NO{sub x}) for circa 1985 and 1990 and Non-Methane Volatile Organic Compounds (NMVOCs) for circa 1990 have been compiled by this project. Work on the inventories has been carried out under the umbrella of the Global Emissions Inventory Activity (GEIA) of the International Global Atmospheric Chemistry (IGAC) Program. The 1985 NO{sub x} inventory was compiled using default data sets of global emissions that were refined via the use of more detailed regional data sets; this inventory is being distributed to the scientific community at large as the GEIA Version 1A inventory. Global emissions of NO{sub x} for 1985 are estimated to be 21 Tg N y{sup -1}, with approximately 84% originating in the Northern Hemisphere. The 1990 inventories of NO{sub x} and NMVOCs were compiled using unified methodologies and data sets in collaboration with the Netherlands National Institute of Public Health and Environmental Protection (Rijksinstituut Voor Volksgezondheid en Milieuhygiene, RIVM) and the Division of Technology for Society of the Netherlands Organization for Applied Scientific Research, (IMW-TNO); these emissions will be used as the default estimates to be updated with more accurate regional data. The NMVOC inventory was gridded and speciated into 23 chemical categories. The resulting global emissions for 1990 are 31 Tg N yr{sup -1} for NO{sub x} and 173 Gg NMVOC yr{sup -1}. Emissions of NO{sub x} are highest in the populated and industrialized areas of eastern North America and across Europe, and in biomass burning areas of South America, Africa, and Asia. Emissions of NMVOCs are highest in biomass burning areas of South America, Africa, and Asia. The 1990 NO{sub x} emissions were gridded to 1{sup o} resolution using surrogate data, and were given seasonal, two-vertical-level resolution and speciated into NO and NO{sub 2} based on proportions derived from the 1985 GEIA Version 1B inventory. Global NMVOC

  5. PTR-MS measurements of non-methane volatile organic compounds during an intensive field campaign at the summit of Mount Tai, China, in June 2006

    NASA Astrophysics Data System (ADS)

    Inomata, S.; Tanimoto, H.; Kato, S.; Suthawaree, J.; Kanaya, Y.; Pochanart, P.; Liu, Y.; Wang, Z.

    2009-12-01

    Owing to recent industrialization, Central East China has become a significant source of air pollutants. To examine the processes controlling the chemistry and transport of tropospheric ozone, we continuously measured non-methane volatile organic compounds (NMVOCs) as part of an intensive field campaign at Mount Tai, China, in June 2006 (MTX2006), using proton transfer reaction mass spectrometry (PTR-MS). Temporal variations of NMVOCs were recorded in mass-scan mode from m/z 17 to m/z 300 during 12-30 June 2006. More than thirty kinds of NMVOCs were detected up to m/z 160, including alkenes, aromatics, alcohols, aldehydes, and ketones. Oxygenated VOCs were the predominant NMVOCs. During the night of 12 June, we observed an episode of high NMVOCs concentrations attributed to the burning of agricultural biomass. The ΔNMVOCs/ΔCO ratios derived by PTR-MS measurements for this episode are compared to emission ratios from various types of biomass burning as reviewed by Andreae and Merlet (2001) and to ratios recently measured by PTR-MS in tropical forests (Karl et al., 2007) and at urban sites (Warneke et al., 2007).

  6. PTR-MS measurements of non-methane volatile organic compounds during an intensive field campaign at the summit of Mount Tai, China, in June 2006

    NASA Astrophysics Data System (ADS)

    Inomata, S.; Tanimoto, H.; Kato, S.; Suthawaree, J.; Kanaya, Y.; Pochanart, P.; Liu, Y.; Wang, Z.

    2010-08-01

    Owing to recent industrialization, Central East China has become a significant source of air pollutants. To examine the processes controlling the chemistry and transport of tropospheric ozone, we performed on-line measurements of non-methane volatile organic compounds (NMVOCs) as part of an intensive field campaign at Mount Tai, China, in June 2006 (MTX2006), using proton transfer reaction mass spectrometry (PTR-MS). Temporal variations of NMVOCs were recorded in mass-scan mode from m/z17 to m/z 300 during 12-30 June 2006. More than thirty kinds of NMVOCs were detected up to m/z 160, including alkenes, aromatics, alcohols, aldehydes, and ketones. In combination with non-methane hydrocarbon data obtained by a gas chromatography with flame ionization detection, it was found that oxygenated VOCs were the predominant NMVOCs. Diurnal variations depending mainly on local photochemistry were observed during 24-28 June. During the night of 12 June, we observed an episode of high NMVOCs concentrations attributed to the burning of agricultural biomass. The ΔNMVOCs/ΔCO ratios derived by PTR-MS measurements for this episode (with biomass burning (BB) plume) and during 16-23 June (without BB plume) are compared to emission ratios from various types of biomass burning as reviewed by Andreae and Merlet (2001) and to ratios recently measured by PTR-MS in tropical forests (Karl et al., 2007) and at urban sites (Warneke et al., 2007).

  7. PTR-MS measurements of non-methane volatile organic compounds during an intensive field campaign at the summit of Mount Tai, China, in June 2006

    NASA Astrophysics Data System (ADS)

    Inomata, Satoshi; Tanimoto, Hiroshi; Kato, Shungo; Suthawaree, Jeeranut; Kanaya, Yugo; Pochanart, Pakpong; Liu, Yu; Wang, Zifa

    2010-05-01

    Owing to recent industrialization, Central East China has become a significant source of air pollutants. To examine the processes controlling the chemistry and transport of tropospheric ozone, we continuously measured non-methane volatile organic compounds (NMVOCs) as part of an intensive field campaign at Mount Tai, China, in June 2006 (MTX2006), using proton transfer reaction mass spectrometry (PTR-MS). Temporal variations of NMVOCs were recorded in mass-scan mode from m/z 17 to m/z 300 during 12-30 June 2006. More than thirty kinds of NMVOCs were detected up to m/z 160, including alkenes, aromatics, alcohols, aldehydes, and ketones. Oxygenated VOCs were the predominant NMVOCs. During the night of 12 June, we observed an episode of high NMVOCs concentrations attributed to the burning of agricultural biomass. The NMVOCs/CO ratios derived by PTR-MS measurements for this episode are compared to emission ratios from various types of biomass burning as reviewed by Andreae and Merlet (2001) and to ratios recently measured by PTR-MS in tropical forests (Karl et al., 2007) and at urban sites (Warneke et al., 2007).

  8. Volatile Organic Compound Emissions by Agricultural Crops

    NASA Astrophysics Data System (ADS)

    Ormeno, E.; Farres, S.; Gentner, D.; Park, J.; McKay, M.; Karlik, J.; Goldstein, A.

    2008-12-01

    Biogenic Volatile Organic Compounds (BVOCs) participate in ozone and aerosol formation, and comprise a substantial fraction of reactive VOC emission inventories. In the agriculturally intensive Central Valley of California, emissions from crops may substantially influence regional air quality, but emission potentials have not been extensively studied with advanced instrumentation for many important crops. Because crop emissions may vary according to the species, and California emission inventories are constructed via a bottom-up approach, a better knowledge of the emission rate at the species-specific level is critical for reducing uncertainties in emission inventories and evaluating emission model performance. In the present study we identified and quantified the BVOCs released by dominant agricultural crops in California. A screening study to investigate both volatile and semivolatile BVOC fractions (oxygenated VOCs, isoprene, monoterepenes, sesquiterpenes, etc.) was performed for 25 crop species (at least 3 replicates plants each), including branch enclosures of woody species (e.g. peach, mandarin, grape, pistachio) and whole plant enclosures for herbaceous species (e.g. onion, alfalfa, carrot), through a dynamic cuvette system with detection by PTRMS, in-situ GCMS/FID, and collection on carbon-based adsorbents followed by extraction and GCMS analysis. Emission data obtained in this study will allow inclusion of these crops in BVOC emission inventories and air quality simulations.

  9. Volatile Organic Compound Emissions from Humans Indoors.

    PubMed

    Tang, Xiaochen; Misztal, Pawel K; Nazaroff, William W; Goldstein, Allen H

    2016-12-06

    Research on the sources of indoor airborne chemicals has traditionally focused on outdoor air, building materials, furnishings, and activities such as smoking, cooking, and cleaning. Relatively little research has examined the direct role of occupant emissions, even though this source clearly contributes to indoor volatile organic compounds (VOCs) and influences indoor chemistry. In this work, we quantify occupant-related gaseous VOC emissions in a university classroom using a proton-transfer-reaction time-of-flight mass spectrometer. Time-resolved concentrations of VOCs in room air and supply air were measured continuously during occupied and unoccupied periods. The emission factor for each human-emitted VOC was determined by dividing the occupant-associated source rate by the corresponding occupancy. Among the most abundant species detected were compounds associated with personal care products. Also prominent were human metabolic emissions, such as isoprene, methanol, acetone, and acetic acid. Additional sources included human skin oil oxidation by ozone, producing compounds such as 4-oxopentanal (4-OPA) and 6-methyl-5-hepten-2-one (6-MHO). By mass, human-emitted VOCs were the dominant source (57%) during occupied periods in a well-ventilated classroom, with ventilation supply air the second most important (35%), and indoor nonoccupant emissions the least (8%). The total occupant-associated VOC emission factor was 6.3 mg h(-1) per person.

  10. Isoprene emission from Indian trees

    NASA Astrophysics Data System (ADS)

    Varshney, C. K.; Singh, Abhai Pratap

    2003-12-01

    Isoprene is the most dominant non-methane volatile organic compound (NMVOC) emitted by plants. NMVOCs play an important role in regulating the composition of atmospheric trace gases including global concentration of tropospheric ozone. Our present knowledge about NMVOCs emission is mainly from studies on temperate tree species. So far information on biogenic NMVOCs emission from tropical tree species is limited. In this study, isoprene emission rates from 40 tropical Indian tree species belonging to 33 genera and 17 families were measured for the first time using a dynamic flow through enclosure chamber technique. The isoprene emission rate from plants (30°C and PAR 1000 μmolm-2s-1) ranged from undetectable to 81.5 μg g-1 h-1 and values were found to be comparable with other studies on tropical tree species. Tree species screened for isoprene emission in the present study may be grouped into the four categories, proposed by [2001], namely, 18 species were negligible or BDL isoprene emitting (<1 μg g-1 h-1), 6 species were low emitting (1 ≤ to <10 μg g-1 h-1), 5 species were moderate emitting (10≤ to <25 μg g-1 h-1), and 11 species were high isoprene emitting (≥25 μg g-1 h-1). Maximum isoprene emission rate (81.5 μg g-1 h-1) was observed in the case of Dalbergia sissoo Linn. It was interesting to find that Citrus limon Linn., Citrus reticulata Linn., Citrus sinensis Linn., Grevillea robusta A. Cunn., and Morus alba Linn., which were earlier reported as BDL or non isoprene emitters in US [, 1998; , 2001] were found to be appreciably high isoprene emitters (0.61-21.60 μg g-1 h-1) in the present study.

  11. Emission inventory of non-methane volatile organic compounds from anthropogenic sources in India

    NASA Astrophysics Data System (ADS)

    Sharma, Sumit; Goel, Anju; Gupta, Divya; Kumar, Atul; Mishra, Arabinda; Kundu, Seema; Chatani, Satoru; Klimont, Zbigniew

    2015-02-01

    This paper presents a new inventory of NMVOC emissions from anthropogenic sources in India for the year 2010. The main new element of this inventory, compared to previous work for India, is the use of new and more detailed data on solvent use sectors and oil production and distribution system. The results are presented at the national and state level for major sectors and VOC species. Finally, the annual emissions were spatially distributed at a fine resolution of 36 × 36 km2 using detailed spatial information. The total anthropogenic NMVOC emissions in India in 2010 were estimated at 9.81 Tg which is in the range of the estimates made in most other studies. The majority of emissions (60%) originated from residential combustion of biomass for cooking. Solvent use sectors and oil production and distribution contributed about 20% followed by transport (12%) and open burning of agricultural residues (7%). Specie-wise distribution shows highest contribution from alkenes and alkynes (38%), followed by alkanes (22%), and aromatics (16%).

  12. Predicting the emission of volatile organic compounds from silage systems

    Technology Transfer Automated Retrieval System (TEKTRAN)

    As a precursor to smog, emission of volatile organic compounds (VOCs) to the atmosphere is an environmental concern in some regions. The major VOC emission source from farms is silage, with emissions coming from the silo face, mixing wagon, and feed bunk. The major compounds emitted are alcohols wit...

  13. GLOBAL INVENTORY OF VOLATILE COMPOUND EMISSIONS FROM ANTHROPOGENIC SOURCES

    EPA Science Inventory

    The report describes a global inventory anthropogenic volatile organic compound (VOC) emissions that includes a separate inventory for each of seven pollutant groups--paraffins, olefins, aromatics, formaldehyde, other aldehydes, other aromatics, and marginally reactive compounds....

  14. EMISSION OF VOLATILE COMPOUNDS BY SEEDS UNDER DIFFERENT ENVIRONMENTAL CONDITIONS

    EPA Science Inventory

    Small mammals locate buried wet seeds more efficiently than buried dry seeds. This may be attributable to emission of volatile compounds by the seeds. To test this hypothesis I measured emission of volatile compounds from seeds of three plant species (Pinus contorta, Purshia tr...

  15. Volatile organic compound emissions from dairy facilities in central California

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Emissions of volatile organic compounds (VOCs) from dairy facilities are thought to be an important contributor to high ozone levels in central California, but emissions inventories from these sources contain significant uncertainties. In this work, VOC emissions were measured at two central Califor...

  16. Non-methane volatile organic compounds in Africa: A view from space

    NASA Astrophysics Data System (ADS)

    Marais, Eloise Ann

    Isoprene emissions affect human health, air quality, and the oxidative capacity of the atmosphere. Globally anthropogenic non-methane volatile organic compounds (NMVOC) emissions are lower than that of isoprene, but local hotspots are hazardous to human health and air quality. In Africa the tropics are a large source of isoprene, while Nigeria appears as a large contributor to regional anthropogenic NMVOC emissions. I make extensive use of space-based formaldehyde (HCHO) observations from the Ozone Monitoring Instrument (OMI) and the chemical transport model (CTM) GEOS-Chem to estimate and examine seasonality of isoprene emissions across Africa, and identify sources and air quality consequences of anthropogenic NMVOC emissions in Nigeria. To estimate isoprene emissions I first developed a filtering scheme to remove (1) contamination from biomass burning and anthropogenic influences; and (2) displacement of HCHO from the isoprene emission source diagnosed with the GEOS-Chem CTM. Conversion to isoprene emissions is with NOx-dependent GEOS-Chem HCHO yields, obtained as the local sensitivity S of the HCHO column ΩHCHO to a perturbation Delta in isoprene emissions EISOP (S = DeltaΩHCHO/DeltaE ISOP). The error in OMI-derived isoprene emissions is 40% at low levels of NOx and 40-90% under high-NOx conditions and is reduced by spatial and temporal averaging to the extent that errors are random. Weak isoprene emission seasonality in equatorial forests is driven predominantly by temperature, while large seasonality in northern and southern savannas is driven by temperature and leaf area index. The largest contribution of African isoprene emissions to surface ozone and particulate matter, determined with GEOS-Chem, of 8 ppbv and 1.5 μg m-3, respectively, is over West Africa. The OMI HCHO data feature a large enhancement over Nigeria that is due to anthropogenic NMVOC emissions. With the OMI HCHO data, coincident satellite observations of atmospheric composition, aircraft

  17. SLCP co-control approach in East Asia: Tropospheric ozone reduction strategy by simultaneous reduction of NOx/NMVOC and methane

    NASA Astrophysics Data System (ADS)

    Akimoto, Hajime; Kurokawa, Jun`ichi; Sudo, Kengo; Nagashima, Tatsuya; Takemura, Toshihiko; Klimont, Zbigniew; Amann, Markus; Suzuki, Katsunori

    2015-12-01

    The emissions of NOx and CO2 in East Asia (Northeast and Southeast Asia) contribute more than 30% of the global total since 2008, and consequently the control of air pollutants and CO2 alleviating regional air pollution and global climate change is of great concern of not only in this region but also worldwide. In order to arrive at a rational view of the short-lived climate pollutants (SLCPs) co-control approach in East Asia, the effectiveness of the reduction of NOx/NMVOC and CH4 emissions for the reduction of tropospheric O3 has been evaluated by individual and simultaneous 50%-reduction of the emissions in Northeast Asia (NEA) using both a global chemical climate model (CHASER/SPRINTARS-MIROC), and a regional chemical transport model (WRF-CMAQ). The simultaneous reduction of NOx/NMVOC and CH4 emissions was found to reduce the regional concentration of surface O3 in NEA, and globally averaged net radiative forcing most effectively. Global mean RF and regional air quality change were also evaluated for the climate stabilization scenario ("450-ppm"), and climate stabilization with additional air pollution mitigation strengthened scenario ("450-ppm-cntr") developed in IIASA with the aid of GAINS model. In the 450 ppm-cntr scenario, emissions of NOx NMVOC, BC and OC were further reduced respectively, for East Asia from the emissions in 450 ppm. The improvement of air quality as well as the mitigation of climate change would grant to the basis of the SLCP co-control approach in East Asia.

  18. Effects of additional nonmethane volatile organic compounds, organic nitrates, and direct emissions of oxygenated organic species on global tropospheric chemistry

    NASA Astrophysics Data System (ADS)

    Ito, Akinori; Sillman, Sanford; Penner, Joyce E.

    2007-03-01

    This work evaluates the sensitivity of tropospheric ozone and its precursors to the representation of nonmethane volatile organic compounds (NMVOCs) and organic nitrates. A global 3-D tropospheric chemistry/transport model (IMPACT) has been exercised initially using the GEOS-Chem chemical reaction mechanism. The model was then extended by adding emissions and photochemical reactions for aromatic and terpenoid hydrocarbons, and by adding explicit representation of hydroxy alkyl nitrates produced from isoprene. Emissions of methanol, phenol, acetic acid and formic acid associated with biomass burning were also added. Results show that O3 increases by 20% in most of the troposphere, peroxyacetyl nitrate (PAN) increases by 30% over much of the troposphere and OH increases by 10%. NOx (NO + NO2) decreases near source regions and increases in remote locations, reflecting increased transport of NOx away from source regions by organic nitrates. The increase in O3 was driven largely by the increased role of PAN as a transporter of NOx and by the rerelease of NOx from isoprene nitrates. The increased PAN production was associated with increases in methyl glyoxal and hydroxyacetone. Comparison with measured values show reasonable agreement for O3 and PAN, but model measurement agreement does not either improve or degrade in the extended model. The extended model shows improved agreement with measurements for methanol, acetic acid and peroxypropional nitrate (PPN). Results from the extended model were consistent with measured alkyl nitrates and glycolaldehyde, but hydroxyacetone and methyl glyoxal were overestimated. The latter suggests that the effect of the isoprene nitrates is somewhat smaller than estimated here. Although the model measurement comparison does not show specific improvements with the extended model, it provides a more complete description of tropospheric chemistry that we believe is important to include.

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

    SciTech Connect

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

    1992-01-01

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

  20. MICROBIAL VOLATILE ORGANIC COMPOUND EMISSION RATES AND EXPOSURE MODEL

    EPA Science Inventory

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

  1. Emission of volatile organic compounds (VOCs) from PVC floor coverings.

    PubMed

    Wiglusz, R; Igielska, B; Sitko, E; Nikel, G; Jarnuszkiewicz, I

    1998-01-01

    In this study 29 PVC floor coverings were tested for emission of vinyl chloride (VC) and other volatile organic compounds (VOCs). A study on the effect of higher temperature on emission of VOCs from newly manufactured PVC flooring was also carried out. The study was conducted in climatic chamber, according to Polish Standard PN-89/Z-04021. GC method was used for analyzing of the compounds emitted. VC was not emitted from any of the floorings tested. Other VOCs were emitted in different concentrations. The influence of temperature on emission was conducted at temperatures of 23 degrees C and 35 degrees C from 2 hrs up to 180 days after introduction of materials in the chamber. The increase of temperature caused increase of total volatile organic compounds (TVOC) emission during 24 hrs of experiment. Then the emission was comparable for both temperatures. After 9 days emission of identified and unidentified compounds (TVOC) showed a rapid decay and stayed on very low level during a few months. The study conducted showed that PVC floorings after 10 days of installation in the room should not be source of indoor air contamination.

  2. Emission of volatile organic compounds from silage: compounds, sources, and implications

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Silage, fermented cattle feed, has recently been identified as a significant source of volatile organic compounds (VOCs) emitted to the atmosphere. A small number of studies have measured VOC emission from silage, but not enough is known about the processes involved to accurately quantify emission r...

  3. Compilation and analyses of emissions inventories for NOAA`s atmospheric chemistry project. Progress report, August 1997

    SciTech Connect

    Benkovitz, C.M.; Mubaraki, M.A.

    1997-09-01

    Global inventories of anthropogenic emissions of oxides of nitrogen (NO{sub x}) for circa 1985 and 1990 and Non-Methane Volatile Organic Compounds (NMVOCs) for circa 1990 have been compiled by this project. Work on the inventories has been carried out under the umbrella of the Global Emissions Inventory Activity (GEIA) of the International Global Atmospheric Chemistry (IGAC) Program. The 1985 NO{sub x} inventory was compiled using default data sets of global emissions that were refined via the use of more detailed regional data sets; this inventory is being distributed to the scientific community at large as the GEIA Version 1A inventory. Global emissions of NO{sub x} for 1985 are estimated to be 21 Tg N y{sup -1}, with approximately 84% originating in the Northern Hemisphere. The 1990 inventories of NO{sub x} and NMVOCs were compiled using unified methodologies and data sets in collaboration with the Netherlands National Institute of Public Health and Environmental Protection (Rijksinstituut Voor Volksgezondheid en Milieuhygiene, RIVM) and the Division of Technology for Society of the Netherlands Organization for Applied Scientific Research, (IMW-TNO); these emissions will be used as the default estimates to be updated with more accurate regional data. The NMVOC inventory was gridded and speciated into 23 chemical categories.

  4. Volatile and semivolatile organic compounds in laboratory peat fire emissions

    NASA Astrophysics Data System (ADS)

    George, Ingrid J.; Black, Robert R.; Geron, Chris D.; Aurell, Johanna; Hays, Michael D.; Preston, William T.; Gullett, Brian K.

    2016-05-01

    In this study, volatile and semi-volatile organic compound (VOCs and SVOCs) mass emission factors were determined from laboratory peat fire experiments. The peat samples originated from two National Wildlife Refuges on the coastal plain of North Carolina, U.S.A. Gas- and particle-phase organic compounds were quantified by gas chromatography-mass spectrometry and by high pressure liquid chromatography. Hazardous air pollutants (HAPs) accounted for a large fraction (∼60%) of the speciated VOC emissions from peat burning, including large contributions of acetaldehyde, formaldehyde, benzene, toluene, and chloromethane. In the fine particle mass (PM2.5), the following organic compound classes were dominant: organic acids, levoglucosan, n-alkanes, and n-alkenes. Emission factors for the organic acids in PM2.5 including n-alkanoic acids, n-alkenoic acids, n-alkanedioic acids, and aromatic acids were reported for the first time for peat burning, representing the largest fraction of organic carbon (OC) mass (11-12%) of all speciated compound classes measured in this work. Levoglucosan contributed to 2-3% of the OC mass, while methoxyphenols represented 0.2-0.3% of the OC mass on a carbon mass basis. Retene was the most abundant particulate phase polycyclic aromatic hydrocarbon (PAH). Total HAP VOC and particulate PAH emissions from a 2008 peat wildfire in North Carolina were estimated, suggesting that peat fires can contribute a large fraction of state-wide HAP emissions.

  5. Emission of charged particles from excited compound nucleus

    SciTech Connect

    Kalandarov, Sh. A.; Adamian, G. G.; Antonenko, N. V.

    2010-11-24

    The formation and decay of excited compound nucleus are studied within the dinuclear system model[1]. The cross sections of complex fragment emission are calculated and compared with experimental data for the reactions {sup 3}He+{sup 108}Ag, {sup 78,82}Kr+{sup 12}C. Angular momentum dependence of cluster emission in {sup 78}Kr+{sup 12}C and {sup 40}Ca+{sup 78}Kr reactions is demonstrated.

  6. Emissions of biogenic volatile organic compounds & their photochemical transformation

    NASA Astrophysics Data System (ADS)

    Yu, Zhujun; Hohaus, Thorsten; Tillmann, Ralf; Andres, Stefanie; Kuhn, Uwe; Rohrer, Franz; Wahner, Andreas; Kiendler-Scharr, Astrid

    2015-04-01

    Natural and anthropogenic activities emit volatile organic compounds (VOC) into the atmosphere. While it is known that land vegetation accounts for 90% of the global VOC emissions, only a few molecules' emission factors are understood. Through VOCs atmospheric oxidation intermediate products are formed. The detailed chemical mechanisms involved are insufficiently known to date and need to be understood for air quality management and climate change predictions. In an experiment using a PTR-ToF-MS with the new-built plant chamber SAPHIR-PLUS in Forschungszentrum Juelich, biogenic emissions of volatile organic compounds (BVOC) from Quercus ilex trees were measured. The BVOC emissions were dominated by monoterpenes, minor emissions of isoprene and methanol were also observed with the overall emission pattern typical for Quercus ilex trees in the growing season. Monoterpenes and isoprene emissions showed to be triggered by light. Additionally, their emissions showed clear exponential temperature dependence under constant light condition as reported in literature. As a tracer for leaf growth, methanol emission showed an abrupt increase at the beginning of light exposure. This is explained as instantaneous release of methanol produced during the night once stomata of leaves open upon light exposure. Emission of methanol showed a near linear increase with temperature in the range of 10 to 35 °C. BVOC were transferred from the plant chamber PLUS to the atmospheric simulation chamber SAPHIR, where their oxidation products from O3 oxidation were measured with PTR-ToF-MS. Gas phase oxidation products such as acetone and acetaldehyde were detected. A quantitative analysis of the data will be presented, including comparison of observations to the Master Chemical Mechanism model.

  7. Measuring Emissions of Volatile Organic Compounds from Silage

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Volatile organic compound (VOC) emissions are considered to be important precursors to smog and ozone production. An experimental protocol was developed to obtain undisturbed silage samples from silage storages. Samples were placed in a wind tunnel where temperature, humidity, and air flow were cont...

  8. Volatile and semivolatile organic compounds in laboratory peat fire emissions

    EPA Science Inventory

    Speciated volatile organic compounds (VOCs) and organic fine particulate matter (PM2.5) mass emission factors were determined from laboratory peat fire experiments. Peat samples originated from two wildlife reserves located near the coast of North Carolina, U.S. Gas and particula...

  9. Volatile organic compound emissions from dry mill fuel ethanol production.

    PubMed

    Brady, Daniel; Pratt, Gregory C

    2007-09-01

    Ethanol fuel production is growing rapidly in the rural Midwest, and this growth presents potential environmental impacts. In 2002, the U.S. Environmental Protection Agency (EPA) and the Minnesota Pollution Control Agency (MPCA) entered into enforcement actions with 12 fuel ethanol plants in Minnesota. The enforcement actions uncovered underreported emissions and resulted in consent decrees that required pollution control equipment be installed. A key component of the consent decrees was a requirement to conduct emissions tests for volatile organic compounds (VOCs) with the goal of improving the characterization and control of emissions. The conventional VOC stack test method was thought to underquantify total VOC emissions from ethanol plants. A hybrid test method was also developed that involved quantification of individual VOC species. The resulting database of total and speciated VOC emissions from 10 fuel ethanol plants is relatively small, but it is the most extensive to date and has been used to develop and gauge compliance with permit limits and to estimate health risks in Minnesota. Emissions were highly variable among facilities and emissions units. In addition to the variability, the small number of samples and the presence of many values below detection limits complicate the analysis of the data. To account for these issues, a nested bootstrap procedure on the Kaplan-Meier method was used to calculate means and upper confidence limits. In general, the fermentation scrubbers and fluid bed coolers emitted the largest mass of VOC emissions. Across most facilities and emissions units ethanol was the pollutant emitted at the highest rate. Acetaldehyde, acetic acid, and ethyl acetate were also important emissions from some units. Emissions of total VOCs, ethanol, and some other species appeared to be a function of the beer feed rate, although the relationship was not reliable enough to develop a production rate-based emissions factor.

  10. Biogenic volatile organic compound emissions from vegetation fires.

    PubMed

    Ciccioli, Paolo; Centritto, Mauro; Loreto, Francesco

    2014-08-01

    The aim of this paper was to provide an overview of the current state of the art on research into the emission of biogenic volatile organic compounds (BVOCs) from vegetation fires. Significant amounts of VOCs are emitted from vegetation fires, including several reactive compounds, the majority belonging to the isoprenoid family, which rapidly disappear in the plume to yield pollutants such as secondary organic aerosol and ozone. This makes determination of fire-induced BVOC emission difficult, particularly in areas where the ratio between VOCs and anthropogenic NOx is favourable to the production of ozone, such as Mediterranean areas and highly anthropic temperate (and fire-prone) regions of the Earth. Fire emissions affecting relatively pristine areas, such as the Amazon and the African savannah, are representative of emissions of undisturbed plant communities. We also examined expected BVOC emissions at different stages of fire development and combustion, from drying to flaming, and from heatwaves coming into contact with unburned vegetation at the edge of fires. We conclude that forest fires may dramatically change emission factors and the profile of emitted BVOCs, thereby influencing the chemistry and physics of the atmosphere, the physiology of plants and the evolution of plant communities within the ecosystem.

  11. Biogenic volatile organic compound emissions from vegetation fires

    PubMed Central

    CICCIOLI, PAOLO; CENTRITTO, MAURO; LORETO, FRANCESCO

    2014-01-01

    The aim of this paper was to provide an overview of the current state of the art on research into the emission of biogenic volatile organic compounds (BVOCs) from vegetation fires. Significant amounts of VOCs are emitted from vegetation fires, including several reactive compounds, the majority belonging to the isoprenoid family, which rapidly disappear in the plume to yield pollutants such as secondary organic aerosol and ozone. This makes determination of fire-induced BVOC emission difficult, particularly in areas where the ratio between VOCs and anthropogenic NOx is favourable to the production of ozone, such as Mediterranean areas and highly anthropic temperate (and fire-prone) regions of the Earth. Fire emissions affecting relatively pristine areas, such as the Amazon and the African savannah, are representative of emissions of undisturbed plant communities. We also examined expected BVOC emissions at different stages of fire development and combustion, from drying to flaming, and from heatwaves coming into contact with unburned vegetation at the edge of fires. We conclude that forest fires may dramatically change emission factors and the profile of emitted BVOCs, thereby influencing the chemistry and physics of the atmosphere, the physiology of plants and the evolution of plant communities within the ecosystem. PMID:24689733

  12. Development of an inventory and temporal allocation profiles of emissions from power plants and industrial facilities in Thailand.

    PubMed

    Pham, Thi Bich Thao; Manomaiphiboon, Kasemsan; Vongmahadlek, Chatchawan

    2008-07-01

    An emission inventory (EI) of power plants and industrial (i.e., non-power plant) facilities in Thailand was developed. Emissions considered are those from fuel consumption (i.e., combustion) for power plants and those from both fuel consumption and industrial processes (i.e., non-combustion) for industrial facilities. For power plants, total annual emissions due to fuel consumption are 107.9 x 10(3) ton NOx (as NO2), 146.2 x 10(3) ton SO2, 6.1 x 10(3) ton NMVOC (non-methane volatile organic compounds), 47.0 x 10(3) ton CO, 1.8 x 10(3) ton NH3, 1.5 x 10(3) ton OC (organic carbon), and 1.5 x 10(3) ton BC (black carbon). For industrial facilities, total annual emissions due to fuel consumption are 111.4 x 10(3) ton NOx (as NO2), 476.9 x 10(3) ton SO2, 33.4 x 10(3) ton NMVOC, 193.1 x 10(3) ton CO, 1.6 x 10(3) ton NH3, 8.5 x 10(3) ton OC, and 8.0 x 10(3) ton BC. Among various industrial types, Food and Beverage, Chemical, and Non-Metal industries are dominant emitters. Total annual emissions due to industrial processes are 79.2 x 10(3) ton SO2, 76.0 x 10(3) ton NMVOC, and 4.8 x 10(3) ton CO. The Central and Eastern regions combined contribute considerably to total emissions for most emission species. Emission estimates found here show fair agreement with those in some selected past studies. A crude estimation of potential fugitive NMVOC emissions specifically from petroleum industry was also made, and the estimates found could be considered significant (nearly half of NMVOC emissions from industrial processes). Several temporal allocation profiles of emissions were also developed and suggested for power plants and industrial facilities, including monthly, daily, and hourly profiles.

  13. Volatile organic compound emission profiles of four common arctic plants

    NASA Astrophysics Data System (ADS)

    Vedel-Petersen, Ida; Schollert, Michelle; Nymand, Josephine; Rinnan, Riikka

    2015-11-01

    The biogenic volatile organic compound (BVOC) emissions from plants impact atmosphere and climate. The species-specific emissions, and thereby the atmospheric impact, of many plant species are still unknown. Knowledge of BVOC emission from arctic plants is particularly limited. The vast area and relatively high leaf temperature give the Arctic potential for emissions that cannot be neglected. This field study aimed to elucidate the BVOC emission profiles for four common arctic plant species in their natural environment during the growing season. BVOCs were sampled from aboveground parts of Empetrum hermaphroditum, Salix glauca, Salix arctophila and Betula nana using the dynamic enclosure technique and collection of volatiles in adsorbent cartridges, analyzed by gas chromatography-mass spectrometry. Sampling occurred three times: in late June/early July, in mid-July and in early August. E. hermaphroditum emitted the least BVOCs, dominated by sesquiterpenes (SQTs) and non-isoprenoid BVOCs. The Salix spp. emitted the most, dominated by isoprene. The emissions of B. nana were composed of about two-thirds non-isoprenoid BVOCs, with moderate amounts of monoterpenes (MTs) and SQTs. The total B. nana emissions and the MT and SQT emissions standardized to 30 °C were highest in the first measurement in early July, while the other species had the highest emissions in the last measurement in early August. As climate change is expected to increase plant biomass and change vegetation composition in the Arctic, the BVOC emissions from arctic ecosystems will also change. Our results suggest that if the abundance of deciduous shrubs like Betula and Salix spp. increases at the expense of slower growing evergreens like E. hermaphroditum, there is the potential for increased emissions of isoprene, MTs and non-isoprenoid BVOCs in the Arctic.

  14. [Carbonyl compounds emission and uptake by plant: Research progress].

    PubMed

    Li, Jian; Cai, Jing; Yan, Liu-Shui; Li, Ling-Na; Tao, Min

    2013-02-01

    This paper reviewed the researches on the carbonyl compounds emission and uptake by plants, and discussed the compensation point of the bidirectional exchange of carbonyl compounds between plants and atmosphere. The uptake by leaf stomata and stratum corneum is the principal way for the purification of air aldehydes by plants. After entering into plant leaves, most parts of carbonyl compounds can be metabolized into organic acid, glucide, amino acid, and carbon dioxide, etc. , by the endoenzymes in leaves. The exchange direction of the carbonyl compounds between plants and atmosphere can be preliminarily predicted by the compensation point and the concentrations of ambient carbonyl compounds. This paper summarized the analytical methods such as DNPH/HPLC/UV and PFPH/GC/MS used for the determination of carbonyl compounds emitted from plants or in plant leaves. The main research interests in the future were pointed out, e. g. , to improve and optimize the analytical methods for the determination of carbonyl compounds emitted from plants and the researches on systems (e. g. , plant-soil system), to enlarge the detection species of carbonyl compounds emitted from plants, to screen the plant species which can effectively metabolize the pollutants, and to popularize the phytoremediation techniques for atmospheric

  15. Volatile Organic Compound Emissions from Dairy Facilities in Central California

    NASA Astrophysics Data System (ADS)

    Hasson, A. S.; Ogunjemiyo, S. O.; Trabue, S.; Middala, S. R.; Ashkan, S.; Scoggin, K.; Vu, K. K.; Addala, L.; Olea, C.; Nana, L.; Scruggs, A. K.; Steele, J.; Shelton, T. C.; Osborne, B.; McHenry, J. R.

    2011-12-01

    Emissions of volatile organic compounds (VOCs) from dairy facilities are thought to be an important contributor to high ozone levels in Central California, but emissions inventories from these sources contain significant uncertainties. In this work, VOC emissions were measured at two Central California dairies during 2010 and 2011. Isolation flux chambers were used to measure direct emissions from specific dairy sources, and upwind/downwind ambient profiles were measured from ground level up to heights of 60 m. Samples were collected using a combination of canisters and sorbent tubes, and were analyzed by GC-MS. Additional in-situ measurements were made using infra-red photoaccoustic detectors and Diode Laser Absorption Spectroscopy. Temperature and ozone profiles up to 250 m above ground level were also measured using a tethersonde. Substantial fluxes of a number of VOCs including alcohols, volatile fatty acids and esters were observed at both sites. Implications of these measurements for regional air quality will be discussed.

  16. Effect of natural compounds on reducing formaldehyde emission from plywood

    NASA Astrophysics Data System (ADS)

    Uchiyama, Shigehisa; Matsushima, Erica; Kitao, Nahoko; Tokunaga, Hiroshi; Ando, Masanori; Otsubo, Yasufumi

    The effects of natural compounds on reducing formaldehyde emission from plywood were investigated. Urea, catechin and vanillin were examined as the natural formaldehyde reducers. The microemission cell, with an internal volume of 35 ml, the maximum exposed test surface area of 177 cm 2 and an air purge flow rate of 50 ml min -1, was used to measure specific emission rate (SER). In the case of no reducer treatment, formaldehyde emission from plywood was fast and SERs were 4.4 mg m -2 h -1 at 30 °C and 15 mg m -2 h -1 at 60 °C. When this plywood was treated with the natural compounds, the SERs of formaldehyde were decreased at all temperatures. In the case of urea treatment, the SERs of formaldehyde decreased to 0.30 mg m -2 h -1 at 30 °C and 0.65 mg m -2 h -1 at 60 °C. When the urea treatment was applied to the inside of kitchen cabinet (made from plywood; 270 cm wide, 60 cm deep, 250 cm high), the concentration of formaldehyde was reduced substantially from 1600 to 130 μg m -3. The reducing effect of formaldehyde continued during the observation period (6 months), with a mean concentration of 100 μg m -3. Reducers in the plywood would react with released formaldehyde. Application of natural compounds such as urea, catechin and vanillin could provide a simple and effective approach for suppressing formaldehyde emission from plywood.

  17. Improved land cover and emission factors for modeling biogenic volatile organic compounds emissions from Hong Kong

    NASA Astrophysics Data System (ADS)

    Leung, D. Y. C.; Wong, P.; Cheung, B. K. H.; Guenther, A.

    2010-04-01

    This paper describes a study of local biogenic volatile organic compounds (BVOC) emissions from the Hong Kong Special Administrative Region (HKSAR). An improved land cover and emission factor database was developed to estimate Hong Kong emissions using MEGAN, a BVOC emission model developed by Guenther et al. (2006). Field surveys of plant species composition and laboratory measurements of emission factors were combined with other data to improve existing land cover and emission factor data. The BVOC emissions from Hong Kong were calculated for 12 consecutive years from 1995 to 2006. For the year 2006, the total annual BVOC emissions were determined to be 12,400 metric tons or 9.82 × 10 9 g C (BVOC carbon). Isoprene emission accounts for 72%, monoterpene emissions account for 8%, and other VOCs emissions account for the remaining 20%. As expected, seasonal variation results in a higher emission in the summer and a lower emission in the winter, with emission predominantly in day time. A high emission of isoprene occurs for regions, such as Lowest Forest-NT North, dominated by broadleaf trees. The spatial variation of total BVOC is similar to the isoprene spatial variation due to its high contribution. The year to year variability in emissions due to weather was small over the twelve-year period (-1.4%, 2006 to 1995 trendline), but an increasing trend in the annual variation due to an increase in forest land cover can be observed (+7%, 2006 to 1995 trendline). The results of this study demonstrate the importance of accurate land cover inputs for biogenic emission models and indicate that land cover change should be considered for these models.

  18. MIX: a mosaic Asian anthropogenic emission inventory for the MICS-Asia and the HTAP projects

    NASA Astrophysics Data System (ADS)

    Li, M.; Zhang, Q.; Kurokawa, J.; Woo, J.-H.; He, K. B.; Lu, Z.; Ohara, T.; Song, Y.; Streets, D. G.; Carmichael, G. R.; Cheng, Y. F.; Hong, C. P.; Huo, H.; Jiang, X. J.; Kang, S. C.; Liu, F.; Su, H.; Zheng, B.

    2015-12-01

    An anthropogenic emission inventory for Asia is developed for the years 2008 and 2010 to support the Model Inter-Comparison Study for Asia (MICS-Asia) and the Task Force on Hemispheric Transport of Air Pollution (TF HTAP) projects by a mosaic of up-to-date regional emission inventories. Emissions are estimated for all major anthropogenic sources in 30 countries and regions in Asia. We conducted detailed comparisons of different regional emission inventories and incorporated the best-available ones for each region into the mosaic inventory at a uniform spatial and temporal resolution. We estimate the total Asian emissions of ten species in 2010 as follows: 51.3 Tg SO2, 52.1 Tg NOx, 336.6 Tg CO, 67.0 Tg NMVOC (non-methane volatile organic compounds), 28.8 Tg NH3, 31.7 Tg PM10, 22.7 Tg PM2.5, 3.5 Tg BC, 8.3 Tg OC and 17.3 Pg CO2. Emissions from China and India dominate the emissions of Asia for most of the species. We also estimated Asian emissions in 2006 using the same methodology of MIX. The relative change rates of Asian emissions for the period of 2006-2010 are estimated as follows: -8.0 % for SO2, +19 % for NOx, +4 % for CO, +15 % for NMVOC, +2 % for NH3, -3 % for PM10, -2 % for PM2.5, +6 % for BC, +2 % for OC and +20 % for CO2. Model-ready speciated NMVOC emissions for SAPRC-99 and CB05 mechanisms were developed following a profile-assignment approach. Monthly gridded emissions at a spatial resolution of 0.25° × 0.25° are developed and can be accessed from http://www.meicmodel.org/dataset-mix.

  19. Evaluation of Volatile Organic Compound Emissions from Megacities and Wildfires

    NASA Astrophysics Data System (ADS)

    Emmons, L. K.; Apel, E. C.; Hornbrook, R. S.; Riemer, D. D.; Lamarque, J.; Wiedinmyer, C.; Mirage Science Team; Arctas Science Team

    2011-12-01

    Volatile organic compounds (VOCs) play a critical role in determining air quality through their impact on ozone production and other pollutants. Tropospheric chemistry models use a variety of treatments for the lumping of VOCs in their chemical mechanisms, as a compromise between detailed treatment and computational speed. However, emission inventories are frequently provided for only total VOCs with little or no information on how to split the emissions among the model species, introducing additional uncertainty to the model simulations. Global model simulations using the Model for Ozone and Related Chemical Tracers (MOZART-4) and several different emission inventories are evaluated through detailed comparison to aircraft and surface observations. In particular, correlations between measured VOCs and CO are used to test the emission inventory emission ratios of the modeled VOC species. For example, megacity VOC emissions will be evaluated with surface measurements in Mumbai, Shanghai and Tokyo, as well as aircraft measurements from the NSF/MIRAGE experiment downwind of Mexico City. Wildfire emissions in Siberia, Canada and California will be evaluated using airborne observations of the NASA/ARCTAS experiment.

  20. Emission characteristics of volatile organic compounds from semiconductor manufacturing.

    PubMed

    Chein, HungMin; Chen, Tzu Ming

    2003-08-01

    A huge amount of volatile organic compounds (VOCs) is produced and emitted with waste gases from semiconductor manufacturing processes, such as cleaning, etching, and developing. VOC emissions from semiconductor factories located at Science-Based Industrial Park, Hsin-chu, Taiwan, were measured and characterized in this study. A total of nine typical semiconductor fabricators (fabs) were monitored over a 12-month period (October 2000-September 2001). A flame ionization analyzer was employed to measure the VOC emission rate continuously in a real-time fashion. The amount of chemical use was adopted from the data that were reported to the Environmental Protection Bureau in Hsin-chu County as per the regulation of the Taiwan Environmental Protection Administration. The VOC emission factor, defined as the emission rate (kg/month) divided by the amount of chemical use (L/month), was determined to be 0.038 +/- 0.016 kg/L. A linear regression equation is proposed to fit the data with the correlation coefficient (R2)=0.863. The emission profiles of VOCs, which were drawn using the gas chromatograph/mass spectrometer analysis method, show that isopropyl alcohol is the dominant compound in most of the fabs.

  1. Volatile organic compound (VOC) emissions during malting and beer manufacture

    NASA Astrophysics Data System (ADS)

    Gibson, Nigel B.; Costigan, Gavin T.; Swannell, Richard P. J.; Woodfield, Michael J.

    Estimates have been made of the amounts of volatile organic compounds (VOCs) released during different stages of beer manufacture. The estimates are based on recent measurements and plant specification data supplied by manufacturers. Data were obtained for three main manufacturing processes (malting, wort processing and fermentation) for three commercial beer types. Some data on the speciation of emitted compounds have been obtained. Based on these measurements, an estimate of the total unabated VOC emission. from the U.K. brewing industry was calculated as 3.5 kta -1, over 95% of which was generated during barley malting. This value does not include any correction for air pollution control.

  2. Emissions of volatile organic compounds (primarily oxygenated species) from pasture

    NASA Astrophysics Data System (ADS)

    Kirstine, Wayne; Galbally, Ian; Ye, Yuerong; Hooper, Martin

    1998-05-01

    The volatile organic compound (VOC) emissions from pasture at a site in southeastern Victoria, Australia, were monitored over a 2 year period using a static chamber technique. Fluxes up to 23,000 μg(C) m-2 h-1 were detected, with the higher fluxes originating from clover rather than from grass species. Gas Chromatographic analyses indicated that emissions from both grass and clover were high in oxygenated hydrocarbons including methanol, ethanol, propanone, butanone, and ethanal, and extremely low in isoprene and monoterpenes. In the case of clover, butanone made up 45-50% of the total emissions. When grass and clover were freshly mown, there were significantly enhanced emissions of VOCs. These enhanced emissions included both those oxygenates emitted from uncut pasture and also C6-oxygenates, including (Z)-3-hexenal, (E)-2-hexenal, (Z)-2-hexen-1-ol, (Z)-3-hexen-l-ol, and (Z)-3-hexenyl acetate. Emissions from the undisturbed pasture increased markedly with temperature and the intensity of solar radiation, peaking at midday and ceasing at night. The fluxes, when normalized to a temperature of 30°C and a light intensity of 1000 μE m-2 s-1 were, for grass and clover respectively, about one eighth and two fifths of the equivalent fluxes reported to occur from U.S. woodlands. The annual integrated emission from the pasture was approximately 1.9 g(C) m-2 or 1.3 mg(C) g-1 (dry matter). The large transient fluxes that occurred following physical damaging of the pasture, when integrated over time, could be of the same order as those emissions that were observed from undisturbed pasture. In the case of methanol, and perhaps ethanol, the emissions from grasslands may be significant global sources of these gases.

  3. Light emission from compound eye with conformal fluorescent coating

    NASA Astrophysics Data System (ADS)

    Martín-Palma, Raúl J.; Miller, Amy E.; Pulsifer, Drew P.; Lakhtakia, Akhlesh

    2015-03-01

    Compound eyes of insects are attractive biological systems for engineered biomimicry as artificial sources of light, given their characteristic wide angular field of view. A blowfly eye was coated with a thin conformal fluorescent film, with the aim of achieving wide field-of-view emission. Experimental results showed that the coated eye emitted visible light and that the intensity showed a weaker angular dependence than a fluorescent thin film deposited on a flat surface.

  4. Emission and deposition of Nitrogen compounds in West Africa

    NASA Astrophysics Data System (ADS)

    Delon, C.; Galy-Lacaux, C.; Adon, M.; Liousse, C.

    2010-12-01

    The atmospheric nitrogen budget depends on emission and deposition fluxes both as reduced and oxidized compounds. In West African ecosystems, data are scarce, and establishing a N budget is not an easy task. This work aims at linking data from diverse origins (surface, aircraft measurements, satellite data, modelling) to estimate emissions and deposition of N compounds in dry and wet savannas of West Africa, and to study their impact on atmospheric chemistry. In remote areas like in the Sahel, N oxidised compounds emissions are dominated by NO biogenic emissions from soils. N emissions from anthropogenic sources (biomass burning, domestic fires, fossil fuel) are less important, due to the low quantity of vegetation, and to the remoteness of big cities. N reduced compounds emissions are dominated by the release of NH3 from cattle dung. Biogenic NO emissions from soils have a direct impact on NOx and O3 concentration increase in the lower troposphere, as shown by results from aircraft and surface measurements, and from modelling (coupled dynamics/chemistry MESONH-C model, with on line emission derived from a neural network algorithm, where the NO flux is dependent on water field pore space, surface and deep soil temperature, sand percentage, pH, fertilization rate and wind speed), in the area of Niamey (Niger) in August 2006. In a second part of this work, estimated emissions of both oxidised and reduced N compounds are compared to estimate dry and wet deposition fluxes for the year 2006 in the Sahel region. The dry deposition flux is the product of modelled dry deposition velocity and the measured concentration. Concentrations have been measured in 3 stations located in dry savanna ecosystem) within the IDAF (IGAC/DEBITS/Africa) network, and dry deposition velocities have been modelled with the surface model ISBA. A first tentative of budget has been calculated for the year 2006, trying to integrate all potentially known sources and sinks in the region. Finally, the

  5. Emission of volatile sulfur compounds from spruce trees

    SciTech Connect

    Rennenberg, H.; Huber, B.; Schroeder, P.; Stahl, K.; Haunold, W.; Georgil, H.W.; Slovik, S.; Pfanz, H. )

    1990-03-01

    Spruce (Picea abies L.) trees from the same clone were supplied with different, but low, amounts of plant available sulfate in the soil (9.7-18.1 milligrams per 100 grams of soil). Branches attached to the trees were enclosed in a dynamic gas exchange cuvette and analyzed for the emission of volatile sulfur compounds. Independent of the sulfate supply in the soil, H{sub 2}S was the predominant reduced sulfur compound continuously emitted from the branches with high rates during the day and low rates in the night. In the light, as well as in the dark, the rates of H{sub 2}S emission increased exponentially with increasing water vapor flux from the needles. Approximately 1 nanomole of H{sub 2}S was found to be emitted per mole of water. When stomata were closed completely, only minute emission of H{sub 2}S was observed. Apparently, H{sub 2}S emission from the needles is highly dependent on stromatal aperture, and permeation through the cuticle is negligible. In several experiments, small amounts of dimethylsulfide and carbonylsulfide were also detected in a portion of the samples. However, SO{sub 2} was the only sulfur compound consistently emitted from branches of spruce trees in addition to H{sub 2}S. Emission of SO{sub 2} mainly proceeded via an outburst starting before the beginning of the light period. The total amount of SO{sub 2} emitted from the needles during this outburst was correlated with the plant available sulfate in the soil. The diurnal changes in sulfur metabolism that may result in an outburst of SO{sub 2} are discussed.

  6. Total non-methane volatile organic compounds (TNMVOC) in the atmosphere of Delhi

    NASA Astrophysics Data System (ADS)

    Kumar Padhy, Pratap; Varshney, C. K.

    Volatile organic compounds (VOC), more specifically, non-methane volatile organic compounds (NMVOC) play a critical role in the atmospheric chemistry. NMVOC, through complex photochemical reactions, contribute to the formation of toxic oxidants, such as tropospheric ozone and PAN, which are injurious to health and highly phytotoxic. Certain NMVOC have been shown to be highly toxic, mutagenic and carcinogenic. NMVOC are receiving increasing attention in the west on account of their implication for human health and air quality. On the other hand, information on NMVOC in India and other developing countries is not available. As a result, appreciation of potential threat from NMVOC in relation to air quality and public health is sadly lacking among planners and policy makers. The paper deals with the estimation of total NMVOC at 13 sites in the urban environment of Delhi during November 1994 to June 1995. An inexpensive, labour intensive manual sample collection device was used and the air samples were analysed using GC-FID. The results show that the amount of NMVOC in the ambient environment of Delhi varied between 1.3 and 32.5 ppmv exhibiting wide temporal and seasonal variation. NMVOC levels mostly peaked at 0900 h, which coincide with the peak traffic hour. The implications of NMVOC build-up in the urban atmosphere are obvious for air quality. The results of this preliminary study make out a strong case for developing a regular monitoring programme for NMVOC in the urban environment of Delhi as well as in other major cities in the region.

  7. How do emission patterns in megacities affect regional air pollution?

    NASA Astrophysics Data System (ADS)

    Heil, A.; Richter, C.; Schroeder, S.; Schultz, M. G.

    2010-12-01

    Megacities around the world show distinctly different emission patterns in terms of absolute amounts and emission ratios of individual chemical compounds due to varying socio-economic developments and technological standards. The emission patterns influence the chemical reactivity of the urban pollution plume, and hence determine air quality in and around megacity areas. In this study, which is part of the European project CITYZEN (megaCITY - Zoom for the ENvironment), the effects of emission changes in four selected megacity areas on air pollution were investigated: BeNeLux (BNL), Istanbul (IST), Pearl River Delta (PRD) and Sao Paulo (SAP). The study aims at answering the question: how would air pollution in megacity X change if it had the same urban emissions per capita as megacity Y? Model simulations with the global chemistry climate model ECHAM5-MOZ were carried out for the year 2001 using a resolution of about 2 degrees in the horizontal and of 31 levels (surface to 10 hPa) in the vertical. The model was driven by meteorological input data from the ECMWF ERA Interim reanalysis. Emissions were taken from the gridded global ACCMIP emission inventory recently established for use in chemistry-climate simulations in connection to the IPCC-AR5 assessments (Lamarque et al. 2010). We carried out sensitivity simulations where emission patterns from each of the megacity areas were replaced by those from all others. This was done on the basis of the per capita emissions for each species and sector averaged over the respective region. Total per capita CO and NMVOC emissions are highest in PRD and lowest in SAP while total per capita NOx emissions are highest in BNL and lowest in SAP. There are strong differences in the relative contribution of the urban sectors to total emissions of individual compounds. As a result, each of the four megacity areas exhibits a very characteristic NMVOC speciation profile which determines the NMVOC-related photochemical ozone (O_3

  8. Oceanic Emissions and Atmospheric Depositions of Volatile Organic Compounds

    NASA Astrophysics Data System (ADS)

    Yang, M.; Blomquist, B.; Beale, R.; Nightingale, P. D.; Liss, P. S.

    2015-12-01

    Atmospheric volatile organic compounds (VOCs) affect the tropospheric oxidative capacity due to their ubiquitous abundance and relatively high reactivity towards the hydroxyal radical. Over the ocean and away from terrestrial emission sources, oxygenated volatile organic compounds (OVOCs) make up a large fraction of VOCs as airmasses age and become more oxidized. In addition to being produced or destroyed in the marine atmosphere, OVOCs can also be emitted from or deposited to the surface ocean. Here we first present direct air-sea flux measurements of three of the most abundant OVOCs - methanol, acetone, and acetaldehyde, by the eddy covariance technique from two cruises in the Atlantic: the Atlantic Meridional Transect in 2012 and the High Wind Gas Exchange Study in 2013. The OVOC mixing ratios were quantified by a high resolution proton-reaction-transfer mass spectrometer with isotopically labeled standards and their air-sea (net) fluxes were derived from the eddy covariance technique. Net methanol flux was consistently from the atmosphere to the surface ocean, while acetone varied from supersaturation (emission) in the subtropics to undersaturation (deposition) in the higher latitudes of the North Atlantic. The net air-sea flux of acetaldehyde is near zero through out the Atlantic despite the apparent supersaturation of this compound in the surface ocean. Knowing the dissolved concentrations and in situ production rates of these compounds in seawater, we then estimate their bulk atmospheric depositions and oceanic emissions. Lastly, we summarize the state of knowledge on the air-sea transport of a number of organic gasses, and postulate the magnitude and environmental impact of total organic carbon transfer between the ocean and the atmosphere.

  9. Prospective air pollutant emissions inventory for the development and production of unconventional natural gas in the Karoo basin, South Africa

    NASA Astrophysics Data System (ADS)

    Altieri, Katye E.; Stone, Adrian

    2016-03-01

    The increased use of horizontal drilling and hydraulic fracturing techniques to produce gas from unconventional deposits has led to concerns about the impacts to local and regional air quality. South Africa has the 8th largest technically recoverable shale gas reserve in the world and is in the early stages of exploration of this resource. This paper presents a prospective air pollutant emissions inventory for the development and production of unconventional natural gas in South Africa's Karoo basin. A bottom-up Monte Carlo assessment of nitrogen oxides (NOx = NO + NO2), particulate matter less than 2.5 μm in diameter (PM2.5), and non-methane volatile organic compound (NMVOC) emissions was conducted for major categories of well development and production activities. NOx emissions are estimated to be 68 tons per day (±42; standard deviation), total NMVOC emissions are 39 tons per day (±28), and PM2.5 emissions are 3.0 tons per day (±1.9). NOx and NMVOC emissions from shale gas development and production would dominate all other regional emission sources, and could be significant contributors to regional ozone and local air quality, especially considering the current lack of industrial activity in the region. Emissions of PM2.5 will contribute to local air quality, and are of a similar magnitude as typical vehicle and industrial emissions from a large South African city. This emissions inventory provides the information necessary for regulatory authorities to evaluate emissions reduction opportunities using existing technologies and to implement appropriate monitoring of shale gas-related activities.

  10. Aromatic compound emissions from municipal solid waste landfill: Emission factors and their impact on air pollution

    NASA Astrophysics Data System (ADS)

    Liu, Yanjun; Lu, Wenjing; Guo, Hanwen; Ming, Zhongyuan; Wang, Chi; Xu, Sai; Liu, Yanting; Wang, Hongtao

    2016-08-01

    Aromatic compounds (ACs) are major components of volatile organic compounds emitted from municipal solid waste (MSW) landfills. The ACs emissions from the working face of a landfill in Beijing were studied from 2014 to 2015 using a modified wind tunnel system. Emission factors (EFs) of fugitive ACs emissions from the working face of the landfill were proposed according to statistical analyses to cope with their uncertainty. And their impacts on air quality were assessed for the first time. Toluene was the dominant AC with an average emission rate of 38.8 ± 43.0 μg m-2 s-1 (at a sweeping velocity of 0.26 m s-1). An increasing trend in AC emission rates was observed from 12:00 to 18:00 and then peaked at 21:00 (314.3 μg m-2 s-1). The probability density functions (PDFs) of AC emission rates could be classified into three distributions: Gaussian, log-normal, and logistic. EFs of ACs from the working face of the landfill were proposed according to the 95th percentile cumulative emission rates and the wind effects on ACs emissions. The annual ozone formation and secondary organic aerosol formation potential caused by AC emissions from landfills in Beijing were estimated to be 8.86 × 105 kg year-1 and 3.46 × 104 kg year-1, respectively. Toluene, m + p-xylene, and 1,3,5-trimethylbenzene were the most significant contributors to air pollution. Although ACs pollutions from landfills accounts for less percentage (∼0.1%) compared with other anthropogenic sources, their fugitive emissions which cannot be controlled efficiently deserve more attention and further investigation.

  11. Emission of volatile organic compounds from silage: Compounds, sources, and implications

    NASA Astrophysics Data System (ADS)

    Hafner, Sasha D.; Howard, Cody; Muck, Richard E.; Franco, Roberta B.; Montes, Felipe; Green, Peter G.; Mitloehner, Frank; Trabue, Steven L.; Rotz, C. Alan

    2013-10-01

    Silage, fermented cattle feed, has recently been identified as a significant source of volatile organic compounds (VOCs) to the atmosphere. A small number of studies have measured VOC emission from silage, but not enough is known about the processes involved to accurately quantify emission rates and identify practices that could reduce emissions. Through a literature review, we have focused on identifying the most important compounds emitted from corn silage (the most common type of silage in the US) and the sources of these compounds by quantifying their production and emission potential in silage and describing production pathways. We reviewed measurements of VOC emission from silage and assessed the importance of individual silage VOCs through a quantitative analysis of VOC concentrations within silage. Measurements of VOC emission from silage and VOCs present within silage indicated that alcohols generally make the largest contribution to emission from corn silage, in terms of mass emitted and potential ozone formation. Ethanol is the dominant alcohol in corn silage; excluding acids, it makes up more than half of the mean mass of VOCs present. Acids, primarily acetic acid, may be important when emission is high and all VOCs are nearly depleted by emission. Aldehydes and esters, which are more volatile than acids and alcohols, are important when exposure is short, limiting emission of more abundant but less volatile compounds. Variability in silage VOC concentrations is very high; for most alcohols and acids, tolerance intervals indicate that 25% of silages have concentrations a factor of two away from median values, and possibly much further. This observation suggests that management practices can significantly influence VOC concentrations. Variability also makes prediction of emissions difficult. The most important acids, alcohols, and aldehydes present in silage are probably produced by bacteria (and, in the case of ethanol, yeasts) during fermentation and

  12. Modeling Emissions of Volatile Organic Compounds from New Carpets

    SciTech Connect

    Little, J.C.; Hodgson, A.T.; Gadgil, A.J.

    1993-02-01

    A simple model is proposed to account for observed emissions of volatile organic compounds (VOCs) from new carpets. The model assumes that the VOCs originate predominantly in a uniform slab of polymer backing material. Parameters for the model (the initial concentration of a VOC in the polymer, a diffusion coefficient and an equilibrium polymer/air partition coefficient) are obtained from experimental data produced by a previous chamber study. The diffusion coefficients generally decrease as the molecular weight of the VOCs increase, while the polymer/air partition coefficients generally increase as the vapor pressure of the compounds decrease. In addition, for two of the study carpets that have a styrene-butadiene rubber (SBR) backing, the diffusion and partition coefficients are similar to independently reported values for SBR. The results suggest that predictions of VOCs emissions from new carpets may be possible based solely on a knowledge of the physical properties of the relevant compounds and the carpet backing material. However, a more rigorous validation of the model is desirable.

  13. Modeling emissions of volatile organic compounds from new carpets

    NASA Astrophysics Data System (ADS)

    Little, John C.; Hodgson, Alfred T.; Gadgil, Ashok J.

    A simple model is proposed to account for observed emissions of volatile organic compounds (VOCs) from new carpets. The model assumes that the VOCs originate predominantly in a uniform slab of polymer backing material. Parameters for the model (the initial concentration of a VOC in the polymer, a diffusion coefficient and an equilibrium polymer/air partition coefficient) are obtained from experimental data produced by a previous chamber study. The diffusion coefficients generally decrease as the molecular weight of the VOCs increase, while the partition coefficients generally increase as the vapor pressure of the compounds decreases. In addition, for two of the study carpets that have a styrene-butadiene rubber (SBR) backing, the diffusion and partition coefficients are similar to independently reported values for SBR. The results suggest that prediction of VOC emissions from new carpets may be possible based solely on a knowledge of the physical properties of the relevant compounds and the carpet backing material. However, a more rigorous validation of the model is desirable.

  14. Emission characteristics of volatile compounds during sludges drying process.

    PubMed

    Deng, Wen-Yi; Yan, Jian-Hua; Li, Xiao-Dong; Wang, Fei; Zhu, Xiao-Wan; Lu, Sheng-Yong; Cen, Ke-Fa

    2009-02-15

    The emission characteristics of volatile compounds (VCs) during municipal sewage sludge (MSS) and paper mill sludge (PMS) drying process were investigated through experiments conducted on a lab-scale tubular drying furnace and a pilot-scale paddle dryer, respectively. The result indicated that five kinds of VCs, i.e. CO(2), NH(3), C(7)H(16) (n-heptane), volatile fatty acids (VFAs) and CH(4) were emitted during the drying process. It was found that the NH(3) and CO(2) were the primary compound released from the MSS drying process. In the case of the PMS, the VFAs and CO(2) were the main compounds released. The temperature and water content of sludge had great effects on the emission rates of NH(3), C(7)H(16), CO(2) and VFAs. The pH and chemical oxygen demand (COD) of condensate from the paddle dryer were also studied. It showed that pH and COD of condensate from MSS were much higher than that from the PMS, and that the higher COD value of the MSS condensate interrelated to the higher ammonium and sulfur content of it.

  15. Determination of urban volatile organic compound emission ratios and comparison with an emissions database

    NASA Astrophysics Data System (ADS)

    Warneke, C.; McKeen, S. A.; de Gouw, J. A.; Goldan, P. D.; Kuster, W. C.; Holloway, J. S.; Williams, E. J.; Lerner, B. M.; Parrish, D. D.; Trainer, M.; Fehsenfeld, F. C.; Kato, S.; Atlas, E. L.; Baker, A.; Blake, D. R.

    2007-05-01

    During the NEAQS-ITCT2k4 campaign in New England, anthropogenic VOCs and CO were measured downwind from New York City and Boston. The emission ratios of VOCs relative to CO and acetylene were calculated using a method in which the ratio of a VOC with acetylene is plotted versus the photochemical age. The intercept at the photochemical age of zero gives the emission ratio. The so determined emission ratios were compared to other measurement sets, including data from the same location in 2002, canister samples collected inside New York City and Boston, aircraft measurements from Los Angeles in 2002, and the average urban composition of 39 U.S. cities. All the measurements generally agree within a factor of two. The measured emission ratios also agree for most compounds within a factor of two with vehicle exhaust data indicating that a major source of VOCs in urban areas is automobiles. A comparison with an anthropogenic emission database shows less agreement. Especially large discrepancies were found for the C2-C4 alkanes and most oxygenated species. As an example, the database overestimated toluene by almost a factor of three, which caused an air quality forecast model (WRF-CHEM) using this database to overpredict the toluene mixing ratio by a factor of 2.5 as well. On the other hand, the overall reactivity of the measured species and the reactivity of the same compounds in the emission database were found to agree within 30%.

  16. Modeling of global biogenic emissions for key indirect greenhouse gases and their response to atmospheric CO2 increases and changes in land cover and climate

    NASA Astrophysics Data System (ADS)

    Tao, Zhining; Jain, Atul K.

    2005-11-01

    Natural emissions of nonmethane volatile organic compounds (NMVOCs) play a crucial role in the oxidation capacity of the lower atmosphere and changes in concentrations of major greenhouse gases (GHGs), particularly methane and tropospheric ozone. In this study, we integrate a global biogenic model within a terrestrial ecosystem model to investigate the vegetation and soil emissions of key indirect GHGs, e.g., isoprene, monoterpene, other NMVOCs (OVOC), CO, and NOx. The combination of a high-resolution terrestrial ecosystem model with satellite data allows investigation of the potential changes in net primary productivity (NPP) and resultant biogenic emissions of indirect GHGs due to atmospheric CO2 increases and changes in climate and land use practices. Estimated global total annual vegetation emissions for isoprene, monoterpene, OVOC, and CO are 601, 103, 102, and 73 Tg C, respectively. Estimated NOx emissions from soils are 7.51 Tg N. The land cover changes for croplands generally lead to a decline of vegetation emissions for isoprene OVOC, whereas temperature and atmospheric CO2 increases lead to higher vegetation emissions. The modeled global mean isoprene emissions show relatively large seasonal variations over the previous 20 years from 1981 to 2000 (as much as 31% from year to year). Savanna and boreal forests show large seasonal variations, whereas tropical forests with high plant productivity throughout the year show small seasonal variations. Results of biogenic emissions from 1981 to 2000 indicate that the CO2 fertilization effect, along with changes in climate and land use, causes the overall up-trend in isoprene and OVOC emissions over the past 2 decades. This relationship suggests that future emission scenario estimations for NMVOCs should account for effects of CO2 and climate in order to more accurately estimate local, regional, and global chemical composition of the atmosphere, the global carbon budget, and radiation balance of the Earth

  17. Characterization of volatile organic compounds from different cooking emissions

    NASA Astrophysics Data System (ADS)

    Cheng, Shuiyuan; Wang, Gang; Lang, Jianlei; Wen, Wei; Wang, Xiaoqi; Yao, Sen

    2016-11-01

    Cooking fume is regarded as one of the main sources of urban atmospheric volatile organic compounds (VOCs) and its chemical characteristics would be different among various cooking styles. In this study, VOCs emitted from four different Chinese cooking styles were collected. VOCs concentrations and emission characteristics were analyzed. The results demonstrated that Barbecue gave the highest VOCs concentrations (3494 ± 1042 μg/m3), followed by Hunan cuisine (494.3 ± 288.8 μg/m3), Home cooking (487.2 ± 139.5 μg/m3), and Shandong cuisine (257.5 ± 98.0 μg/m3). The volume of air drawn through the collection hood over the stove would have a large impact on VOCs concentration in the exhaust. Therefore, VOCs emission rates (ER) and emission factors (EF) were also estimated. Home cooking had the highest ER levels (12.2 kg/a) and Barbecue had the highest EF levels (0.041 g/kg). The abundance of alkanes was higher in Home cooking, Shandong cuisine and Hunan cuisine with the value of 59.4%-63.8%, while Barbecue was mainly composed of alkanes (34.7%) and alkenes (39.9%). The sensitivity species of Home cooking and Hunan cuisine were alkanes, and that of Shandong cuisine and Barbecue were alkenes. The degree of stench pollution from cooking fume was lighter.

  18. Management of tropospheric ozone by reducing methane emissions.

    PubMed

    West, J Jason; Fiore, Arlene M

    2005-07-01

    Background concentrations of tropospheric ozone are increasing and are sensitive to methane emissions, yet methane mitigation is currently considered only for climate change. Methane control is shown here to be viable for ozone management. Identified global abatement measures can reduce approximately 10% of anthropogenic methane emissions at a cost-savings, decreasing surface ozone by 0.4-0.7 ppb. Methane controls produce ozone reductions that are widespread globally and are realized gradually (approximately 12 yr). In contrast, controls on nitrogen oxides (NOx) and nonmethane volatile organic compounds (NMVOCs) target high-ozone episodes in polluted regions and affect ozone rapidly but have a smaller climate benefit. A coarse estimate of the monetized global benefits of ozone reductions for agriculture, forestry, and human health (neglecting ozone mortality) justifies reducing approximately 17% of global anthropogenic methane emissions. If implemented, these controls would decrease ozone by -1 ppb and radiative forcing by approximately 0.12 W m(-2). We also find that climate-motivated methane reductions have air quality-related ancillary benefits comparable to those for CO2. Air quality planning should consider reducing methane emissions alongside NOx and NMVOCs, and because the benefits of methane controls are shared internationally, industrialized nations should consider emphasizing methane in the further development of climate change or ozone policies.

  19. Identification of nonmethane organic compound emissions from grassland vegetation.

    SciTech Connect

    Fukui, Y.; Doskey, P. V.; Environmental Research; NASA Ames Research Center

    2000-01-01

    Emissions of nonmethane organic compounds (NMOCs) from grassland vegetation were collected in Summa(reg.sign) passivated stainless-steel canisters with a static enclosure technique and were analyzed by high-resolution gas chromatography with flame ionization and ion trap mass spectrometric detectors. Approximately 40 NMOCs with 6-10 carbon atoms were observed in samples analyzed by high-resolution gas chromatography with the flame ionization detector. Nineteen NMOCs in this molecular weight range (6 aliphatic oxygenates; 1 aromatic hydrocarbon; and 4 acyclic, 5 monocyclic, and 3 bicyclic monoterpenoids) were identified by ion trap mass spectrometry. Mass spectrometry was particularly useful for identifying myrcene and cis-3-hexenylacetate, which coeluted on a fused-silica capillary column coated with a 1-{mu}m-thick film of polydimethylsiloxane. An evaluation of the reactivity of the grassland emissions revealed that the aliphatic oxygenates have lifetimes of a few hours with respect to oxidation by OH and O{sub 3} in the atmosphere. This value is similar to the lifetimes of the bicyclic monoterpenoids. The expected lifetimes of the monoterpenoids with respect to oxidation by NO{sub 3} are only several minutes.

  20. VOLATILE ORGANIC COMPOUND EMISSION RATES FROM MIXED DECIDUOUS AND CONIFEROUS FORESTS IN NORTHERN WISCONSIN, USA

    EPA Science Inventory

    Biogenic emissions of volatile organic compounds (VOC) from forests play an important role in regulating the atmospheric trace gas composition including global tropospheric ozone concentrations. However, more information is needed on VOC emission rates from different forest regio...

  1. 78 FR 55234 - Approval and Promulgation of Implementation Plans; Indiana; Volatile Organic Compound Emission...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-09-10

    ... Compound Emission Control Measures for Industrial Solvent Cleaning for Northwest Indiana AGENCY: Environmental Protection Agency (EPA). ACTION: Proposed rule. SUMMARY: On May 29, 2012, the Indiana Department of Environmental Management (IDEM) submitted revisions to its volatile organic compound...

  2. On-line measurements of emissions and atmospheric fate of compounds from agricultural waste management

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Agricultural emissions impact air quality on a local and regional basis. Research on the emissions and reduction of greenhouse gases from agriculture has become commonplace due to concerns about climate but other chemical compounds also impact air quality. These include compounds that are photochemi...

  3. [Establishment and improvement of emission control standard system of volatile organic compounds in industry].

    PubMed

    Jiang, Mei; Zhang, Guo-Ning; Zou, Lan; Wei, Yu-Xia; Zhang, Ming-Hui

    2013-12-01

    Volatile organic compounds (VOCs) has become one of the priority control pollutants, due to the regional compound pollution problem represented by atmospheric haze. Through the analysis of the present situation for current national and local emission standards of VOCs, the pollution characteristics and the emission inventory of VOCs, a basic standard system of VOCs has been proposed and improved.

  4. [Emission control way of volatile organic compounds in industry].

    PubMed

    Jiang, Mei; Zhang, Guo-Ning; Wei, Yu-Xia; Zou, Lan; Zhang, Ming-Hui

    2011-12-01

    Due to the volatile nature, the way of controlling way of VOCs was different from other atmospheric pollutants. By analyzing the emission characteristics of VOCs, four kinds of control way were proposed, which were the source control, organized emission control, fugitive emission control and the total amount control, and the control modes of each control way were also analyzed and compared.

  5. Atmospheric nitrogen compounds II: emissions, transport, transformation, deposition and assessment

    NASA Astrophysics Data System (ADS)

    Aneja, Viney P.; Roelle, Paul A.; Murray, George C.; Southerland, James; Erisman, Jan Willem; Fowler, David; Asman, Willem A. H.; Patni, Naveen

    The Atmospheric Nitrogen Compounds II: Emissions, Transport, Transformation, Deposition and Assessment workshop was held in Chapel Hill, NC from 7 to 9 June 1999. This international conference, which served as a follow-up to the workshop held in March 1997, was sponsored by: North Carolina Department of Environment and Natural Resources; North Carolina Department of Health and Human Services, North Carolina Office of the State Health Director; Mid-Atlantic Regional Air Management Association; North Carolina Water Resources Research Institute; Air and Waste Management Association, RTP Chapter; the US Environmental Protection Agency and the North Carolina State University (College of Physical and Mathematical Sciences, and North Carolina Agricultural Research Service). The workshop was structured as an open forum at which scientists, policy makers, industry representatives and others could freely share current knowledge and ideas, and included international perspectives. The workshop commenced with international perspectives from the United States, Canada, United Kingdom, the Netherlands, and Denmark. This article summarizes the findings of the workshop and articulates future research needs and ways to address nitrogen/ammonia from intensively managed animal agriculture. The need for developing sustainable solutions for managing the animal waste problem is vital for shaping the future of North Carolina. As part of that process, all aspects of environmental issues (air, water, soil) must be addressed as part of a comprehensive and long-term strategy. There is an urgent need for North Carolina policy makers to create a new, independent organization that will build consensus and mobilize resources to find technologically and economically feasible solutions to this aspect of the animal waste problem.

  6. The Study of Biogenetic Organic Compound Emissions and Ozone in a Subtropical Bamboo Forest

    NASA Astrophysics Data System (ADS)

    Bai, Jianhui; Guenther, Alex; Turnipseed, Andrew; Duhl, Tiffany; Duhl, Nanhao; van der A, Ronald; Yu, Shuquan; Wang, Bin

    2016-08-01

    Emissions of Biogenic Volatile Organic compounds (BVOCs), Photosynthetically Active Radiation (PAR), and meteorological parameters were measured in some ecosystems in China. A Relaxed Eddy Accumulation system and an enclosure technique were used to measure BVOC emissions. Obvious diurnal and seasonal variations of BVOC emissions were found. Empirical models of BVOC emissions were developed, the estimated BVOC emissions were in agreement with observations. BVOC emissions in growing seasons in the Inner Mongolia grassland, Chnagbai Mountain temperate forest, LinAn subtropical bamboo forest were estimated. The emission factors of these ecosystems were calculated.

  7. Economic development and multiple air pollutant emissions from the industrial sector.

    PubMed

    Fujii, Hidemichi; Managi, Shunsuke

    2016-02-01

    This study analyzed the relationship between economic growth and emissions of eight environmental air pollutants (carbon dioxide (CO2), methane (CH4), nitrous oxide (N2O), nitrogen oxide (NOx), sulfur oxide (SOx), carbon monoxide (CO), non-methane volatile organic compound (NMVOC), and ammonia (NH3)) in 39 countries from 1995 to 2009. We tested an environmental Kuznets curve (EKC) hypothesis for 16 individual industry sectors and for the total industrial sector. The results clarified that at least ten individual industries do not have an EKC relationship in eight air pollutants even though this relationship was observed in the country and total industrial sector level data. We found that the key industries that dictated the EKC relationship in the country and the total industrial sector existed in CO2, N2O, CO, and NMVOC emissions. Finally, the EKC turning point and the relationship between economic development and trends of air pollutant emissions differ among industries according to the pollution substances. These results suggest inducing new environmental policy design such as the sectoral crediting mechanism, which focuses on the industrial characteristics of emissions.

  8. Potential application of biocover soils to landfills for mitigating toluene emission.

    PubMed

    Su, Yao; Pei, Junshen; Tian, Baohu; Fan, Fengxi; Tang, Mengling; Li, Wei; He, Ruo

    2015-12-15

    Biocover soils have been demonstrated to be a good alternative cover material to mitigate CH4 emission from landfills. To evaluate the potential of biocover soil in mitigating emissions of non-methane volatile organic compounds (NMVOCs) from landfills, simulated cover soil columns with the influx of toluene (chosen as typical of NMVOCs) concentrations of 102-1336 mg m(-3) in the presence or absence of the major landfill gas components (i.e., CH4 and CO2) were conducted in this study. In the two experimental materials (waste biocover soils (WBS) and landfill cover soils (LCS)), higher toluene reduction was observed in WBS with respect to LCS. After the introduction of landfill gas, an increase of microbial diversity and relative abundance of toluene-degrading bacteria and methanotrophs occurred in WBS. To illustrate the role of toluene-degrading activity in mitigating toluene emissions through landfill covers, an analytical model was developed by incorporating the steady-state vapor transport with the first-order kinetics of aerobic biodegradation limited by O2 availability. This study demonstrated that biocover soils have great potential in applying to landfills for mitigating toluene emission to the atmosphere.

  9. Temporal variation of trace compound emission on the working surface of a landfill in Beijing, China

    NASA Astrophysics Data System (ADS)

    Duan, Zhenhan; Lu, Wenjing; Li, Dong; Wang, Hongtao

    2014-05-01

    The temporal variation of trace component emissions from the working surface of a landfill in Beijing was investigated. Specific days in a year were selected as representatives for all four seasons. Different chemical species were quantified in all four seasons with the following average concentrations: spring: 41 compounds, 2482.6 μg m-3; summer: 59 compounds, 4512.6 μg m-3; fall: 66 compounds, 2438.4 μg m-3; and winter: 54 compounds, 2901 μg m-3. The detected compounds included sulfur compounds, oxygenated compounds, aromatics, hydrocarbons, halogenated compounds, and terpenes. Oxygenated compounds were the most abundant compound in most samples. Isobutane, ethyl alcohol, limonene, butane, toluene, and trichlorofluoromethane were recognized as the most abundant compounds on the working surface throughout the year. This study would bring new light in assessing the particle pollution in urban areas and the effect of trace components on landfill odor.

  10. Global emissions and models of photochemically active compounds

    SciTech Connect

    Penner, J.E.; Atherton, C.S.; Graedel, T.E.

    1993-05-20

    Anthropogenic emissions from industrial activity, fossil fuel combustion, and biomass burning are now known to be large enough (relative to natural sources) to perturb the chemistry of vast regions of the troposphere. A goal of the IGAC Global Emissions Inventory Activity (GEIA) is to provide authoritative and reliable emissions inventories on a 1{degree} {times} 1{degree} grid. When combined with atmospheric photochemical models, these high quality emissions inventories may be used to predict the concentrations of major photochemical products. Comparison of model results with measurements of pertinent species allows us to understand whether there are major shortcomings in our understanding of tropospheric photochemistry, the budgets and transport of trace species, and their effects in the atmosphere. Through this activity, we are building the capability to make confident predictions of the future consequences of anthropogenic emissions. This paper compares IGAC recommended emissions inventories for reactive nitrogen and sulfur dioxide to those that have been in use previously. We also present results from the three-dimensional LLNL atmospheric chemistry model that show how emissions of anthropogenic nitrogen oxides might potentially affect tropospheric ozone and OH concentrations and how emissions of anthropogenic sulfur increase sulfate aerosol loadings.

  11. NATURAL EMISSIONS OF NON-METHANE VOLATILE ORGANIC COMPOUNDS, CARBON MONOXIDE, AND OXIDES OF NITROGEN FROM NORTH AMERICA

    EPA Science Inventory

    The magnitudes, distributions, controlling processes and uncertainties associated with North American natural emissions of oxidant precursors are reviewed. Natural emissions are repsonsible for a major portion of the compounds, including non-methane volatile organic compounds (N...

  12. 77 FR 46961 - Approval and Promulgation of Implementation Plans; Wisconsin; Volatile Organic Compound Emission...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-08-07

    ... AGENCY 40 CFR Part 52 Approval and Promulgation of Implementation Plans; Wisconsin; Volatile Organic... Volatile Organic Compound (VOC) emissions in moderate ozone nonattainment areas. Wisconsin's VOC rules..., Intergovernmental relations, Nitrogen dioxide, Ozone, Reporting and recordkeeping requirements, Volatile...

  13. VOLATILE ORGANIC COMPOUNDS FROM VEGETATION IN SOUTHERN YUNNAN PROVINCE, CHINA: EMISSION RATES AND SOME POTENTIAL REGIONAL IMPLICATIONS

    EPA Science Inventory

    Little information is currently available regarding emissions of biogenic volatile organic compounds (BVOCs) in southern Asia. To address the need for BVOC emission estimates in regional atmospheric chemistry simulations, 95 common plant species were screened for emissions of BVO...

  14. Measurements of biogenic non-methane organic compound emissions from grasslands

    SciTech Connect

    Fukui, Yoshiko

    1994-12-31

    Non-methane organic compounds (NMOCs) play an important role in the formation of photochemical oxidants in the troposphere. NMOCs originate from both anthropogenic and biogenic sources. Many organic compounds of biogenic origins are more reactive than those of anthropogenic origin because of the presence of internal double bonds within their molecular structure. The objective of this investigation was to examine the seasonal variation of NMOC emissions from grasslands and determine the environmental factors that control the emissions. An enclosure system was chosen as the most appropriate sampling technique for measuring emissions from herbaceous vegetation, and an analysis method using cryogenic preconcentration/high resolution gas chromatography was established. Emission rates were measured at a fixed location in a natural grassland during 1992 and 1993. Measurements were also made at various locations within the same site where the vegetation was harvested after the emission rates were determined. Emission rates of NMOCs for grasslands are not as large as those reported for forests. However the emissions of oxygenated hydrocarbons exceeded the emissions of monoterpenes and have not previously been identified as important forest-type emissions. A framework for parameterizing the NMOC emissions from grasslands based on seasonal and instantaneous variations of the emission rate measurements was developed. Temperature, hypoxia induced by water saturated soil, and frost were key environmental factors affecting both the composition and magnitude of NMOC emissions.

  15. The impact of anthropogenic and biogenic emissions on surface ozone concentrations in Istanbul.

    PubMed

    Im, Ulas; Poupkou, Anastasia; Incecik, Selahattin; Markakis, Konstantinos; Kindap, Tayfun; Unal, Alper; Melas, Dimitros; Yenigun, Orhan; Topcu, Sema; Odman, M Talat; Tayanc, Mete; Guler, Meltem

    2011-03-01

    Surface ozone concentrations at Istanbul during a summer episode in June 2008 were simulated using a high resolution and urban scale modeling system coupling MM5 and CMAQ models with a recently developed anthropogenic emission inventory for the region. Two sets of base runs were performed in order to investigate for the first time the impact of biogenic emissions on ozone concentrations in the Greater Istanbul Area (GIA). The first simulation was performed using only the anthropogenic emissions whereas the second simulation was performed using both anthropogenic and biogenic emissions. Biogenic NMVOC emissions were comparable with anthropogenic NMVOC emissions in terms of magnitude. The inclusion of biogenic emissions significantly improved the performance of the model, particularly in reproducing the low night time values as well as the temporal variation of ozone concentrations. Terpene emissions contributed significantly to the destruction of the ozone during nighttime. Biogenic NMVOCs emissions enhanced ozone concentrations in the downwind regions of GIA up to 25ppb. The VOC/NO(x) ratio almost doubled due to the addition of biogenic NMVOCs. Anthropogenic NO(x) and NMVOCs were perturbed by ±30% in another set of simulations to quantify the sensitivity of ozone concentrations to the precursor emissions in the region. The sensitivity runs, as along with the model-calculated ozone-to-reactive nitrogen ratios, pointed NO(x)-sensitive chemistry, particularly in the downwind areas. On the other hand, urban parts of the city responded more to changes in NO(x) due to very high anthropogenic emissions.

  16. Emission of charged particles from excited compound nuclei

    SciTech Connect

    Kalandarov, Sh. A.; Adamian, G. G.; Antonenko, N. V.; Scheid, W.

    2010-10-15

    The process of complex fragment emission is studied within the dinuclear system model. Cross sections of complex fragment emission are calculated and compared with experimental data for the reactions {sup 3}He+{sup nat}Ag, {sup 78,86}Kr+{sup 12}C, and {sup 63}Cu+{sup 12}C. The mass distributions of the products of these reactions, isotopic distributions for the {sup 3}He+{sup nat}Ag and {sup 78}Kr+{sup 12}C reactions, and average total kinetic energies of the products of the {sup 78}Kr+{sup 12}C reaction are predicted.

  17. Competition between the compound and the pre-compound emission processes in α-induced reactions at near astrophysical energy to well above it

    NASA Astrophysics Data System (ADS)

    Sharma, Manoj Kumar; Sharma, Vijay Raj; Yadav, Abhiskek; Singh, Pushpendra P.; Singh, B. P.; Prasad, R.

    2016-04-01

    The study of pre-compound emission in α-induced reactions, particularly at the low incident energies, is of considerable interest as the pre-compound emission is more likely to occur at higher energies. With a view to study the competition between the compound and the pre-compound emission processes in α-induced reactions at different energies and with different targets, a systematics for neutron emission channels in targets 51V, 55Mn, 93Nb, 121, 123Sb and 141Pr at energy ranging from astrophysical interest to well above it, has been developed. The off-line γ-ray-spectrometry based activation technique has been adopted to measure the excitation functions. The experimental excitation functions have been analysed within the framework of the compound nucleus mechanism based on the Weisskopf-Ewing model and the pre-compound emission calculations based on the geometry dependent hybrid model. The analysis of the data shows that experimental excitation functions could be reproduced only when the pre-compound emission, simulated theoretically, is taken into account. The strength of pre-compound emission process for each system has been obtained by deducing the pre-compound fraction. Analysis of data indicates that in α-induced reactions, the pre-compound emission process plays an important role, particularly at the low incident energies, where the pure compound nucleus process is likely to dominate.

  18. 40 CFR 60.502 - Standard for Volatile Organic Compound (VOC) emissions from bulk gasoline terminals.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... (VOC) emissions from bulk gasoline terminals. 60.502 Section 60.502 Protection of Environment... SOURCES Standards of Performance for Bulk Gasoline Terminals § 60.502 Standard for Volatile Organic Compound (VOC) emissions from bulk gasoline terminals. On and after the date on which § 60.8(a) requires...

  19. 40 CFR 60.502 - Standard for Volatile Organic Compound (VOC) emissions from bulk gasoline terminals.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... (VOC) emissions from bulk gasoline terminals. 60.502 Section 60.502 Protection of Environment... SOURCES Standards of Performance for Bulk Gasoline Terminals § 60.502 Standard for Volatile Organic Compound (VOC) emissions from bulk gasoline terminals. On and after the date on which § 60.8(a) requires...

  20. 40 CFR 60.502 - Standard for Volatile Organic Compound (VOC) emissions from bulk gasoline terminals.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... (VOC) emissions from bulk gasoline terminals. 60.502 Section 60.502 Protection of Environment... SOURCES Standards of Performance for Bulk Gasoline Terminals § 60.502 Standard for Volatile Organic Compound (VOC) emissions from bulk gasoline terminals. On and after the date on which § 60.8(a) requires...

  1. 40 CFR 60.502 - Standard for Volatile Organic Compound (VOC) emissions from bulk gasoline terminals.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... (VOC) emissions from bulk gasoline terminals. 60.502 Section 60.502 Protection of Environment... SOURCES Standards of Performance for Bulk Gasoline Terminals § 60.502 Standard for Volatile Organic Compound (VOC) emissions from bulk gasoline terminals. On and after the date on which § 60.8(a) requires...

  2. Speciation of volatile organic compound emissions for regional air quality modeling of particulate matter and ozone

    NASA Astrophysics Data System (ADS)

    Makar, P. A.; Moran, M. D.; Scholtz, M. T.; Taylor, A.

    2003-01-01

    A new classification scheme for the speciation of organic compound emissions for use in air quality models is described. The scheme uses 81 organic compound classes to preserve both net gas-phase reactivity and particulate matter (PM) formation potential. Chemical structure, vapor pressure, hydroxyl radical (OH) reactivity, freezing point/boiling point, and solubility data were used to create the 81 compound classes. Volatile, semivolatile, and nonvolatile organic compounds are included. The new classification scheme has been used in conjunction with the Canadian Emissions Processing System (CEPS) to process 1990 gas-phase and particle-phase organic compound emissions data for summer and winter conditions for a domain covering much of eastern North America. A simple postprocessing model was used to analyze the speciated organic emissions in terms of both gas-phase reactivity and potential to form organic PM. Previously unresolved compound classes that may have a significant impact on ozone formation include biogenic high-reactivity esters and internal C6-8 alkene-alcohols and anthropogenic ethanol and propanol. Organic radical production associated with anthropogenic organic compound emissions may be 1 or more orders of magnitude more important than biogenic-associated production in northern United States and Canadian cities, and a factor of 3 more important in southern U.S. cities. Previously unresolved organic compound classes such as low vapour pressure PAHs, anthropogenic diacids, dialkyl phthalates, and high carbon number alkanes may have a significant impact on organic particle formation. Primary organic particles (poorly characterized in national emissions databases) dominate total organic particle concentrations, followed by secondary formation and primary gas-particle partitioning. The influence of the assumed initial aerosol water concentration on subsequent thermodynamic calculations suggests that hydrophobic and hydrophilic compounds may form external

  3. 78 FR 24990 - Approval and Promulgation of Implementation Plans; Ohio; Volatile Organic Compound Emission...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-04-29

    ... AGENCY 40 CFR Part 52 Approval and Promulgation of Implementation Plans; Ohio; Volatile Organic Compound...), several volatile organic compound (VOC) rules that were submitted by the Ohio Environmental Protection... emissions from stationary sources, storage of volatile organic liquids, industrial cleaning solvents,...

  4. Formation and emission of volatile polonium compound by microbial activity and polonium methylation with methylcobalamin.

    PubMed

    Momoshima, N; Song, L X; Osaki, S; Maeda, Y

    2001-07-15

    We observed biologically mediated emission of Po from culture solution inoculated sea sediment extract and incubated under natural light/dark cycle condition or dark condition the emitted Po compound would be lipophilic because of effective collection in organic solvent. Sterilization of the culture medium with antibiotics or CuSO4 completely suppressed growth of microorganisms and resulted in no emission of Po, indicating biological activity of microorganisms is responsible for formation and emission of volatile Po compound. Po emission also occurred when seawater was used as a culture medium. Our finding indicates a possibility of biotic source for atmospheric Po in the environment, which has been believed to be originated from abiotic sources. We compared emission behavior of Po and S in the culture experiments, the elements belong to XVI group in the Periodical Table, and consider that their emission mechanisms involved would be different though the emission of both elements is supported by biological activity of microorganisms. One of the chemical forms of S emitted was confirmed to be dimethyl sulfide (DMS) but that of Po is not known. Methylation experiments of Po with methylcobalamin demonstrated a formation and emission of volatile Po compound. The methylation of Po with methylcobalamin might be related to the observed Po emission in the culture experiments.

  5. Compound specific carbon and hydrogen stable isotope analyses of volatile organic compounds in various emissions of combustion processes.

    PubMed

    Vitzthum von Eckstaedt, Christiane D; Grice, Kliti; Ioppolo-Armanios, Marisa; Kelly, David; Gibberd, Mark

    2012-11-01

    This study presents carbon (δ(13)C) and hydrogen (δD) isotope values of volatile organic compounds (VOCs) in various emission sources using thermal desorption-gas chromatography-isotope ratio mass spectrometry (TD-GC-irMS). The investigated VOCs ranged from C6 to C10. Samples were taken from (i) car exhaust emissions as well as from plant combustion experiments of (ii) various C3 and (iii) various C4 plants. We found significant differences in δ values of analysed VOCs between these sources, e.g. δ(13)C of benzene ranged between (i) -21.7 ± 0.2 ‰, (ii) -27.6 ± 1.6 ‰ and (iii) -16.3 ± 2.2 ‰, respectively and δD of benzene ranged between (i) -73 ± 13 ‰, (ii) -111 ± 10 ‰ and (iii) -70 ± 24 ‰, respectively. Results of VOCs present in investigated emission sources were compared to values from the literature (aluminium refinery emission). All source groups could be clearly distinguished using the dual approach of δ(13)C and δD analysis. The results of this study indicate that the correlation of compound specific carbon and hydrogen isotope analysis provides the potential for future research to trace the fate and to determine the origin of VOCs in the atmosphere using thermal desorption compound specific isotope analysis.

  6. Modeling emissions of volatile organic compounds from silage

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Photochemical smog is a major air pollution problem and a significant cause of premature death in the U.S. Smog forms in the presence of volatile organic compounds (VOCs), which are emitted primarily from industry and motor vehicles in the U.S. However, dairy farms may be an important source in so...

  7. Modeling emissions of volatile organic compounds from silage

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Volatile organic compounds (VOCs), necessary reactants for photochemical smog formation, are emitted from numerous sources. Limited available data suggest that dairy farms emit VOCs with cattle feed, primarily silage, being the primary source. Process-based models of VOC transfer within and from si...

  8. MEASUREMENT OF ORGANIC COMPOUND EMISSIONS USING SMALL TEST CHAMBERS

    EPA Science Inventory

    Organic compounds emitted from a variety of indoor materials have been measured using small (166 L) environmental test chambers. The paper discusses: a) factors to be considered in small chamber testing; b) parameters to be controlled; c) the types of results obtained. The follow...

  9. Modeling toxic compounds from nitric oxide emission measurements

    NASA Astrophysics Data System (ADS)

    Vallero, Daniel A.; Peirce, Jeffrey; Cho, Ki Don

    Determining the amount and rate of degradation of toxic pollutants in soil and groundwater is difficult and often requires invasive techniques, such as deploying extensive monitoring well networks. Even with these networks, degradation rates across entire systems cannot readily be extrapolated from the samples. When organic compounds are degraded by microbes, especially nitrifying bacteria, oxides or nitrogen (NO x) are released to the atmosphere. Thus, the flux of nitric oxide (NO) from the soil to the lower troposphere can be used to predict the rate at which organic compounds are degraded. By characterizing and applying biogenic and anthropogenic processes in soils the rates of degradation of organic compounds. Toluene was selected as a representative of toxic aromatic compounds, since it is inherently toxic, it is a substituted benzene compound and is listed as a hazardous air pollutant under Section 12 of the Clean Air Act Amendments of 1990. Measured toluene concentrations in soil, microbial population growth and NO fluxes in chamber studies were used to develop and parameterize a numerical model based on carbon and nitrogen cycling. These measurements, in turn, were used as indicators of bioremediation of air toxic (i.e. toluene) concentrations. The model found that chemical concentration, soil microbial abundance, and NO production can be directly related to the experimental results (significant at P < 0.01) for all toluene concentrations tested. This indicates that the model may prove useful in monitoring and predicting the fate of toxic aromatic contaminants in a complex soil system. It may also be useful in predicting the release of ozone precursors, such as changes in reservoirs of hydrocarbons and oxides of nitrogen. As such, the model may be a tool for decision makers in ozone non-attainment areas.

  10. Regional atmospheric emissions determined from measurements at Jeju Island, Korea: Halogenated compounds from China

    NASA Astrophysics Data System (ADS)

    Kim, Jooil; Li, Shanlan; Kim, Kyung-Ryul; Stohl, Andreas; Mühle, Jens; Kim, Seung-Kyu; Park, Mi-Kyung; Kang, Dong-Jin; Lee, Gangwoong; Harth, Christina M.; Salameh, Peter K.; Weiss, Ray F.

    2010-06-01

    High-frequency in-situ measurements of a wide range of halogenated compounds including chlorofluorocarbons (CFCs), halons, hydrochlorofluorocarbons (HCFCs), hydrofluorocarbons (HFCs), perfluorinated compounds (PFCs), sulfur hexafluoride (SF6), and other chlorinated and brominated compounds have been made at Gosan (Jeju Island, Korea). Regional emissions of HCFC-22 (CHClF2) calculated from inverse modeling were combined with interspecies correlation methods to estimate national emissions for China, a major emitter of industrial halogenated gases. Our results confirm the signs of successful phase-out of primary ozone-depleting species such as CFCs, halons and many chlorinated or brominated compounds, along with substantial emissions of replacement HCFCs. Emissions derived for HFCs, PFCs, and SF6 were compared to published estimates and found to be a significant fraction of global totals. Overall, Chinese emissions of the halogenated compounds discussed here represent 19(14-17)% and 20(15-26)% of global emissions when evaluated in terms of their Ozone Depletion Potentials and 100-year Global Warming Potentials, respectively.

  11. Development of a biogenic volatile organic compounds emission inventory for the SCOS97-NARSTO domain

    NASA Astrophysics Data System (ADS)

    Scott, Klaus I.; Benjamin, Michael T.

    The Biogenic Emission Inventory Geographic Information System (BEIGIS) is a spatially and temporally resolved biogenic hydrocarbon emissions inventory model developed by the California Air Resources Board that uses California land use/land cover, leaf mass, and emission rate databases within a GIS. BEIGIS simulates hourly emissions of isoprene, monoterpenes, and 2-methyl-3-buten-2-ol (MBO, methylbutenol) at a 1 km 2 resolution. When applied to the Southern California Ozone Study (SCOS97-NARSTO) domain for the 3-7 August 1997 ozone episode, the BEIGIS model predicts total biogenic volatile organic compound (BVOC) emissions of 866 tons for the warmest day (5 August). Depending on whether wildfire emissions are included in the total volatile organic compound (VOC) emissions estimate, modeled BVOC emissions comprise between 16% and 28% of the total VOC inventory. As anthropogenic VOC emissions decline in future years due to control programs, the relative significance of BVOC emissions in the development of ozone control strategies for southern California may assume greater importance.

  12. Toxic volatile organic compounds in environmental tobacco smoke: Emission factors for modeling exposures of California populations

    SciTech Connect

    Daisey, J.M.; Mahanama, K.R.R.; Hodgson, A.T.

    1994-10-01

    The primary objective of this study was to measure emission factors for selected toxic air contaminants in environmental tobacco smoke (ETS) using a room-sized environmental chamber. The emissions of 23 volatile organic compounds (VOCs), including, 1,3-butadiene, three aldehydes and two vapor-phase N-nitrosamines were determined for six commercial brands of cigarettes and reference cigarette 1R4F. The commercial brands were selected to represent 62.5% of the cigarettes smoked in California. For each brand, three cigarettes were machine smoked in the chamber. The experiments were conducted over four hours to investigate the effects of aging. Emission factors of the target compounds were also determined for sidestream smoke (SS). For almost all target compounds, the ETS emission factors were significantly higher than the corresponding SS values probably due to less favorable combustion conditions and wall losses in the SS apparatus. Where valid comparisons could be made, the ETS emission factors were generally in good agreement with the literature. Therefore, the ETS emission factors, rather than the SS values, are recommended for use in models to estimate population exposures from this source. The variabilities in the emission factors ({mu}g/cigarette) of the selected toxic air contaminants among brands, expressed as coefficients of variation, were 16 to 29%. Therefore, emissions among brands were Generally similar. Differences among brands were related to the smoked lengths of the cigarettes and the masses of consumed tobacco. Mentholation and whether a cigarette was classified as light or regular did not significantly affect emissions. Aging was determined not to be a significant factor for the target compounds. There were, however, deposition losses of the less volatile compounds to chamber surfaces.

  13. Cold temperature and biodiesel fuel effects on speciated emissions of volatile organic compounds from diesel trucks.

    PubMed

    George, Ingrid J; Hays, Michael D; Snow, Richard; Faircloth, James; George, Barbara J; Long, Thomas; Baldauf, Richard W

    2014-12-16

    Speciated volatile organic compounds (VOCs) were measured in diesel exhaust from three heavy-duty trucks equipped with modern aftertreatment technologies. Emissions testing was conducted on a chassis dynamometer at two ambient temperatures (-7 and 22 °C) operating on two fuels (ultra low sulfur diesel and 20% soy biodiesel blend) over three driving cycles: cold start, warm start and heavy-duty urban dynamometer driving cycle. VOCs were measured separately for each drive cycle. Carbonyls such as formaldehyde and acetaldehyde dominated VOC emissions, making up ∼ 72% of the sum of the speciated VOC emissions (∑VOCs) overall. Biodiesel use led to minor reductions in aromatics and variable changes in carbonyls. Cold temperature and cold start conditions caused dramatic enhancements in VOC emissions, mostly carbonyls, compared to the warmer temperature and other drive cycles, respectively. Different 2007+ aftertreatment technologies involving catalyst regeneration led to significant modifications of VOC emissions that were compound-specific and highly dependent on test conditions. A comparison of this work with emission rates from different diesel engines under various test conditions showed that these newer technologies resulted in lower emission rates of aromatic compounds. However, emissions of other toxic partial combustion products such as carbonyls were not reduced in the modern diesel vehicles tested.

  14. Large drought-induced variations in oak leaf volatile organic compound emissions during PINOT NOIR 2012

    SciTech Connect

    Geron, Chris; Gu, Lianhong; Daly, Ryan; Harley, Peter; Rasmussen, Rei; Seco, Roger; Guenther, Alex; Karl, Thomas

    2015-12-17

    Here, leaf-level isoprene and monoterpene emissions were collected and analyzed from five of the most abundant oak (Quercus) species in Central Missouri's Ozarks Region in 2012 during PINOT NOIR (Particle Investigations at a Northern Ozarks Tower – NOx, Oxidants, Isoprene Research). June measurements, prior to the onset of severe drought, showed isoprene emission rates and leaf temperature responses similar to those previously reported in the literature and used in Biogenic Volatile Organic Compound (BVOC) emission models. During the peak of the drought in August, isoprene emission rates were substantially reduced, and response to temperature was dramatically altered, especially for the species in the red oak subgenus (Erythrobalanus).

  15. Secondary electron emission from lithium and lithium compounds

    DOE PAGES

    Capece, A. M.; Patino, M. I.; Raitses, Y.; ...

    2016-07-06

    In this work, measurements of electron-induced secondary electron emission ( SEE) yields of lithium as a function of composition are presented. The results are particularly relevant for magnetic fusion devices such as tokamaks, field-reversed configurations, and stellarators that consider Li as a plasma-facing material for improved plasma confinement. SEE can reduce the sheath potential at the wall and cool electrons at the plasma edge, resulting in large power losses. These effects become significant as the SEE coefficient, γe, approaches one, making it imperative to maintain a low yield surface. This work demonstrates that the yield from Li strongly depends onmore » chemical composition and substantially increases after exposure to oxygen and water vapor. The total yield was measured using a retarding field analyzer in ultrahigh vacuum for primary electron energies of 20-600 eV. The effect of Li composition was determined by introducing controlled amounts of O2 and H2O vapor while monitoring film composition with Auger electron spectroscopy and temperature programmed desorption. The results show that the energy at which γe = 1 decreases with oxygen content and is 145 eV for a Li film that is 17% oxidized and drops to less than 25 eV for a fully oxidized film. This work has important implications for laboratory plasmas operating under realistic vacuum conditions in which oxidation significantly alters the electron emission properties of Li walls. Published by AIP Publishing.« less

  16. Dielectric barrier discharge carbon atomic emission spectrometer: universal GC detector for volatile carbon-containing compounds.

    PubMed

    Han, Bingjun; Jiang, Xiaoming; Hou, Xiandeng; Zheng, Chengbin

    2014-01-07

    It was found that carbon atomic emission can be excited in low temperature dielectric barrier discharge (DBD), and an atmospheric pressure, low power consumption, and compact microplasma carbon atomic emission spectrometer (AES) was constructed and used as a universal and sensitive gas chromatographic (GC) detector for detection of volatile carbon-containing compounds. A concentric DBD device was housed in a heating box to increase the plasma operation temperature to 300 °C to intensify carbon atomic emission at 193.0 nm. Carbon-containing compounds directly injected or eluted from GC can be decomposed, atomized, and excited in this heated DBD for carbon atomic emission. The performance of this new optical detector was first evaluated by determination of a series of volatile carbon-containing compounds including formaldehyde, ethyl acetate, methanol, ethanol, 1-propanol, 1-butanol, and 1-pentanol, and absolute limits of detection (LODs) were found at a range of 0.12-0.28 ng under the optimized conditions. Preliminary experimental results showed that it provided slightly higher LODs than those obtained by GC with a flame ionization detector (FID). Furthermore, it is a new universal GC detector for volatile carbon-containing compounds that even includes those compounds which are difficult to detect by FID, such as HCHO, CO, and CO2. Meanwhile, hydrogen gas used in conventional techniques was eliminated; and molecular optical emission detection can also be performed with this GC detector for multichannel analysis to improve resolution of overlapped chromatographic peaks of complex mixtures.

  17. Emissions of isoprene, monoterpene and short-chained carbonyl compounds from Eucalyptus spp. in southern Australia

    NASA Astrophysics Data System (ADS)

    Winters, Anthony J.; Adams, Mark A.; Bleby, Tim M.; Rennenberg, Heinz; Steigner, Dominik; Steinbrecher, Rainer; Kreuzwieser, Jürgen

    Eucalypts are among the highest emitters of biogenic volatile organic compounds, yet there is relatively little data available from field studies of this genus. Emissions of isoprene, monoterpenes and the short-chained carbonyls formaldehyde, acetaldehyde and acetone were determined from four species ( Eucalyptus camaldulensis, Eucalyptus globulus, Eucalyptus grandis, and Eucalytpus viminalis) in Australia. A smaller comparative study was conducted on E. camaldulensis in south-eastern Australia. Carbonyl emissions, reported here for the first time from eucalypts, were generally comparable with rates reported for other species, with diurnal emissions peaking at about 4, 75 and 34 nmol m -2 min -1 for acetone, formaldehyde and acetaldehyde respectively. There was wide variation in diurnal isoprene and monoterpene emissions between species, but under standard conditions, isoprene emissions were much lower than previous reports. Conversely, standard emission rates of monoterpenes were as much as six times greater than previous reports for some species. Emission of each carbonyl was correlated with its ambient concentration across different species, but more weakly related to temperature. Acetaldehyde emission in particular was significantly correlated with transpiration, but not with sap flow or with ethanol concentrations in xylem sap, suggesting fermentation within the leaf and stomatal conductance are primary controlling processes. Differences in acetaldehyde exchange velocities between sites, in addition to transpiration differences, suggest stomata may indeed exert long term emission regulation, in contrast to compounds for which no biological sink exists.

  18. Global inventory of volatile organic compound emissions from anthropogenic sources. Final report, March 1988-September 1990

    SciTech Connect

    Watson, J.J.; Probert, J.A.; Piccot, S.D.

    1991-01-01

    The report describes a global inventory of anthropogenic volatile organic compound (VOC) emissions that includes a separate inventory for each of seven pollutant groups--paraffins, olefins, aromatics, formaldehyde, other aldehydes, other aromatics, and marginally reactive compounds. The inventory, one input to atmospheric chemistry models required to estimate the global atmospheric concentration of ozone, is part of an assessment of the potential environmental impacts associated with global climate change. Study results show total global anthropogenic emissions of about 121 million short tons of VOCs per year. The U.S. is the largest emitter with 21% of the total. Globally, fuelwood combustion and savanna burning are the largest sources, together accounting for over 35% of global VOC emissions. The approach used to develop the inventory involved: (1) identifying the major anthropogenic sources of VOC emissions in the U.S. and grouping them into categories; (2) developing emission factors by dividing the U.S. emissions by the amount of production or consumption of the related commodity in the U.S.; (3) multiplying the U.S. emission factors by production/consumption statistics for other countries to yield global VOC emission estimates; and (4) geographically distributing the emissions.

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

    PubMed

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

    2000-09-01

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

  20. Production and emission of volatile compounds by petal cells.

    PubMed

    Baudino, Sylvie; Caissard, Jean-Claude; Bergougnoux, Véronique; Jullien, Frédéric; Magnard, Jean-Louis; Scalliet, Gabriel; Cock, J Mark; Hugueney, Philippe

    2007-11-01

    We localized the tissues and cells that contribute to scent biosynthesis in scented and non-scented Rosa x hybrida cultivars as part of a detailed cytological analysis of the rose petal. Adaxial petal epidermal cells have a typical conical, papillate shape whereas abaxial petal epidermal cells are flat. Using two different techniques, solid/liquid phase extraction and headspace collection of volatiles, we showed that, in roses, both epidermal layers are capable of producing and emitting scent volatiles, despite the different morphologies of the cells of these two tissues. Moreover, OOMT, an enzyme involved in scent molecule biosynthesis, was localized in both epidermal layers. These results are discussed in view of results found in others species such as Antirrhinum majus, where it has been shown that the adaxial epidermis is the preferential site of scent production and emission.

  1. Production and Emission of Volatile Compounds by Petal Cells

    PubMed Central

    Caissard, Jean-Claude; Bergougnoux, Véronique; Jullien, Frédéric; Magnard, Jean-Louis; Scalliet, Gabriel; Cock, J Mark; Hugueney, Philippe

    2007-01-01

    We localized the tissues and cells that contribute to scent biosynthesis in scented and non-scented Rosa × hybrida cultivars as part of a detailed cytological analysis of the rose petal. Adaxial petal epidermal cells have a typical conical, papillate shape whereas abaxial petal epidermal cells are flat. Using two different techniques, solid/liquid phase extraction and headspace collection of volatiles, we showed that, in roses, both epidermal layers are capable of producing and emitting scent volatiles, despite the different morphologies of the cells of these two tissues. Moreover, OOMT, an enzyme involved in scent molecule biosynthesis, was localized in both epidermal layers. These results are discussed in view of results found in others species such as Antirrhinum majus, where it has been shown that the adaxial epidermis is the preferential site of scent production and emission. PMID:19704548

  2. Secondary electron emission from lithium and lithium compounds

    SciTech Connect

    Capece, A. M.; Patino, M. I.; Raitses, Y.; Koel, B. E.

    2016-07-06

    In this work, measurements of electron-induced secondary electron emission ( SEE) yields of lithium as a function of composition are presented. The results are particularly relevant for magnetic fusion devices such as tokamaks, field-reversed configurations, and stellarators that consider Li as a plasma-facing material for improved plasma confinement. SEE can reduce the sheath potential at the wall and cool electrons at the plasma edge, resulting in large power losses. These effects become significant as the SEE coefficient, γe, approaches one, making it imperative to maintain a low yield surface. This work demonstrates that the yield from Li strongly depends on chemical composition and substantially increases after exposure to oxygen and water vapor. The total yield was measured using a retarding field analyzer in ultrahigh vacuum for primary electron energies of 20-600 eV. The effect of Li composition was determined by introducing controlled amounts of O2 and H2O vapor while monitoring film composition with Auger electron spectroscopy and temperature programmed desorption. The results show that the energy at which γe = 1 decreases with oxygen content and is 145 eV for a Li film that is 17% oxidized and drops to less than 25 eV for a fully oxidized film. This work has important implications for laboratory plasmas operating under realistic vacuum conditions in which oxidation significantly alters the electron emission properties of Li walls. Published by AIP Publishing.

  3. Changes in Emissions in Megacities during the Past Decades: Impact on the Distribution of Atmospheric Compounds

    NASA Astrophysics Data System (ADS)

    Doumbia, E. H. T.; Granier, C.; Sindelarova, K.; Tilmes, S.; Bouarar, I.; Richter, A.; Hilboll, A.; Conley, A. J.; Garcia, R. R.; Kinnison, D. E.; Lamarque, J. F.; Marsh, D. R.; Smith, A. K.; Neely, R.; Turnock, S.

    2015-12-01

    The surface emissions of atmospheric compounds have changed dramatically in many world regions during the past decades. We will evaluate these changes through an analysis of different global and regional anthropogenic emissions inventories, focusing on several megacities. In European and North American megacities, surface emissions of chemical compounds have decreased significantly, while they have increased in many other megacities in different parts of the world. Simulations performed with the CAM4-Chem Community Earth System Model will be used to evaluate the impact of the changes in emissions on the distributions chemical compounds in different megacities. These simulations were performed as part of the Chemistry-Climate Model Initiative (CCMI), a project of the International Global Atmospheric Chemistry Project (IGAC). The analysis of the simulations will focus more particularly on nitrogen dioxide: this species has been observed by satellite measurements since the late 1990s. Model results and satellite observations will be analysed for everal megacities in Europe and North America, where strong emission controls have been implemented. Other megacities in China, India, Africa and South America, where few emission regulations have been enforced have seen large increases in their emissions: we will evaluate the consistency of the model simulations and satellite observations of NO2 in these cities.

  4. Emission estimates of selected volatile organic compounds from tropical savanna burning in northern Australia

    NASA Astrophysics Data System (ADS)

    Shirai, T.; Blake, D. R.; Meinardi, S.; Rowland, F. S.; Russell-Smith, J.; Edwards, A.; Kondo, Y.; Koike, M.; Kita, K.; Machida, T.; Takegawa, N.; Nishi, N.; Kawakami, S.; Ogawa, T.

    2003-02-01

    Here we present measurements of a range of carbon-based compounds: carbon dioxide (CO2), carbon monoxide (CO), methane (CH4), nonmethane hydrocarbons (NMHCs), methyl halides, and dimethyl sulfide (DMS) emitted by Australian savanna fires studied as part of the Biomass Burning and Lightning Experiment (BIBLE) phase B aircraft campaign, which took place during the local late dry season (28 August to 13 September 1999). Significant enhancements of short-lived NMHCs were observed in the boundary layer (BL) over the region of intensive fires and indicate recent emissions for which the mean transport time was estimated to be about 9 hours. Emission ratios relative to CO were determined for 20 NMHCs, 3 methyl halides, DMS, and CH4 based on the BL enhancements in the source region. Tight correlations with CO were obtained for most of those compounds, indicating the homogeneity of the local savanna source. The emission ratios were in good agreement with some previous measurements of savanna fires for stable compounds but indicated the decay of emission ratios during transport for several reactive compounds. Based on the observed emission ratios, emission factors were derived and compared to previous studies. While emission factors (g species/kg dry mole) of CO2 varied little according to the vegetation types, those of CO and NMHCs varied significantly. Higher combustion efficiency and a lower emission factor for methane in this study, compared to forest fires, agreed well with results for savanna fires in other tropical regions. The amount of biomass burned was estimated by modeling methods using available satellite data, and showed that 1999 was an above average year for savanna burning. The gross emissions of the trace gases from Australian savanna fires were estimated.

  5. Effects of climate change on volatile organic compound emissions from soil and litter

    NASA Astrophysics Data System (ADS)

    Gray, C. M.; Fierer, N.

    2012-12-01

    Our knowledge of the variability and magnitude of volatile organic compound (VOC) emissions from soil and litter is relatively limited compared to what we know about VOC emissions from terrestrial plants. With climate change expecting to alter plant community composition, nitrogen (N) deposition rates, mean annual temperatures, and precipitation patterns, it is unknown how production and consumption of VOCs from litter and soil will respond. We spent the last four years quantifying VOC emissions from soil and litter, comparing VOC emissions to CO2 emissions, and identifying the biotic and abiotic controls on emission rates with both lab and field experiments using a proton transfer reaction mass spectrometer (PTR-MS). In all studies, methanol was the dominant VOC flux. VOC emissions were not driven by abiotic processes, as microbial sources accounted for 78% to 99% of the total VOC emissions from decomposing litter. Litter chemistry was correlated with the types of VOCs emitted and the net emissions of carbon as VOCs was found to be up to 88% of that emitted as CO2 suggesting that VOCs likely represent an important component of the carbon cycle in many terrestrial systems. Nitrogen additions drastically reduced VOC emissions from litter to near zero, though it is still not understood whether this was due to an increase in consumption or a decrease in production. Finally, field and lab experiments show that temperature and moisture are both important controls of certain VOC emissions from soils, but that the effects of these factors on VOC emissions are not necessarily equivalent to their effects on CO2 emissions. Together, these series of studies are moving us toward a predictive understanding of VOC emissions from soil and litter with the ultimate goal of incorporating these VOC emissions into global models of terrestrial VOC dynamics.

  6. MIX: a mosaic Asian anthropogenic emission inventory under the international collaboration framework of the MICS-Asia and HTAP

    NASA Astrophysics Data System (ADS)

    Li, Meng; Zhang, Qiang; Kurokawa, Jun-ichi; Woo, Jung-Hun; He, Kebin; Lu, Zifeng; Ohara, Toshimasa; Song, Yu; Streets, David G.; Carmichael, Gregory R.; Cheng, Yafang; Hong, Chaopeng; Huo, Hong; Jiang, Xujia; Kang, Sicong; Liu, Fei; Su, Hang; Zheng, Bo

    2017-01-01

    The MIX inventory is developed for the years 2008 and 2010 to support the Model Inter-Comparison Study for Asia (MICS-Asia) and the Task Force on Hemispheric Transport of Air Pollution (TF HTAP) by a mosaic of up-to-date regional emission inventories. Emissions are estimated for all major anthropogenic sources in 29 countries and regions in Asia. We conducted detailed comparisons of different regional emission inventories and incorporated the best available ones for each region into the mosaic inventory at a uniform spatial and temporal resolution. Emissions are aggregated to five anthropogenic sectors: power, industry, residential, transportation, and agriculture. We estimate the total Asian emissions of 10 species in 2010 as follows: 51.3 Tg SO2, 52.1 Tg NOx, 336.6 Tg CO, 67.0 Tg NMVOC (non-methane volatile organic compounds), 28.8 Tg NH3, 31.7 Tg PM10, 22.7 Tg PM2.5, 3.5 Tg BC, 8.3 Tg OC, and 17.3 Pg CO2. Emissions from China and India dominate the emissions of Asia for most of the species. We also estimated Asian emissions in 2006 using the same methodology of MIX. The relative change rates of Asian emissions for the period of 2006-2010 are estimated as follows: -8.1 % for SO2, +19.2 % for NOx, +3.9 % for CO, +15.5 % for NMVOC, +1.7 % for NH3, -3.4 % for PM10, -1.6 % for PM2.5, +5.5 % for BC, +1.8 % for OC, and +19.9 % for CO2. Model-ready speciated NMVOC emissions for SAPRC-99 and CB05 mechanisms were developed following a profile-assignment approach. Monthly gridded emissions at a spatial resolution of 0.25° × 0.25° are developed and can be accessed from http://www.meicmodel.org/dataset-mix.

  7. Plant-specific volatile organic compound emission rates from young and mature leaves of Mediterranean vegetation

    NASA Astrophysics Data System (ADS)

    Bracho-Nunez, Araceli; Welter, Saskia; Staudt, Michael; Kesselmeier, Jürgen

    2011-08-01

    The seasonality of vegetation, i.e., developmental stages and phenological processes, affects the emission of volatile organic compounds (VOCs). Despite the potential significance, the contributions of seasonality to VOC emission quality and quantity are not well understood and are therefore often ignored in emission simulations. We investigated the VOC emission patterns of young and mature leaves of several Mediterranean plant species in relation to their physiological and developmental changes during the growing period and estimated Es. Foliar emissions of isoprenoids and oxygenated VOCs like methanol and acetone were measured online by means of a proton transfer reaction mass spectrometer (PTR-MS) and offline with gas chromatography coupled with a mass spectrometer and flame ionization detector. The results suggest that VOC emission is a developmentally regulated process and that quantitative and qualitative variability is plant species specific. Leaf ontogeny clearly influenced both the VOC Es and the relative importance of different VOCs. Methanol was the major compound contributing to the sum of target VOC emissions in young leaves (11.8 ± 10.4 μg g-1 h-1), while its contribution was minor in mature leaves (4.1 ± 4.1 μg g-1 h-1). Several plant species showed a decrease or complete subsidence of monoterpene, sesquiterpene, and acetone emissions upon maturity, perhaps indicating a potential response to the higher defense demands of young emerging leaves.

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

    SciTech Connect

    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.

  9. Development of a test method for carbonyl compounds from stationary source emissions

    SciTech Connect

    Zhihua Fan; Peterson, M.R.; Jayanty, R.K.M.

    1997-12-31

    Carbonyl compounds have received increasing attention because of their important role in ground-level ozone formation. The common method used for the measurement of aldehydes and ketones is 2,4-dinitrophenylhydrazine (DNPH) derivatization followed by high performance liquid chromatography and ultra violet (HPLC-UV) analysis. One of the problems associated with this method is the low recovery for certain compounds such as acrolein. This paper presents a study in the development of a test method for the collection and measurement of carbonyl compounds from stationary source emissions. This method involves collection of carbonyl compounds in impingers, conversion of carbonyl compounds to a stable derivative with O-2,3,4,5,6-pentafluorobenzyl hydroxylamine hydrochloride (PFBHA), and separation and measurement by electron capture gas chromatography (GC-ECD). Eight compounds were selected for the evaluation of this method: formaldehyde, acetaldehyde, acrolein, acetone, butanal, methyl ethyl ketone (MEK), methyl isobutyl ketone (MIBK), and hexanal.

  10. Selective detection of carbon-13-labeled compounds by gas chromatography/emission spectroscopy

    SciTech Connect

    Quimby, B.D.; Dryden, P.C.; Sullivan, J.J. )

    1990-11-15

    This paper describes a technique which also provides selective GC detection of compounds with excess {sup 13}C content. Molecular emission from CO bands in the vacuum ultraviolet region is monitored with an atomic emission detector (AED) (4,5). Samples can also be analyzed for C, H, O, N, S, P, Cl, F, etc. by changing the reagent and makeup gas flows. This combination of {sup 13}C specificity with atomic information is useful in the identification of unknown compounds, especially when combined with mass spectral data, as shown by Hooker and DeZwaan (6).

  11. Comparison of carbonyl compounds emissions from diesel engine fueled with biodiesel and diesel

    NASA Astrophysics Data System (ADS)

    He, Chao; Ge, Yunshan; Tan, Jianwei; You, Kewei; Han, Xunkun; Wang, Junfang; You, Qiuwen; Shah, Asad Naeem

    The characteristics of carbonyl compounds emissions were investigated on a direct injection, turbocharged diesel engine fueled with pure biodiesel derived from soybean oil. The gas-phase carbonyls were collected by 2,4-dinitrophenylhydrazine (DNPH)-coated silica cartridges from diluted exhaust and analyzed by HPLC with UV detector. A commercial standard mixture including 14 carbonyl compounds was used for quantitative analysis. The experimental results indicate that biodiesel-fueled engine almost has triple carbonyls emissions of diesel-fueled engine. The weighted carbonyls emission of 8-mode test cycle of biodiesel is 90.8 mg (kW h) -1 and that of diesel is 30.7 mg (kW h) -1. The formaldehyde is the most abundant compound of carbonyls for both biodiesel and diesel, taking part for 46.2% and 62.7% respectively. The next most significant compounds are acetaldehyde, acrolein and acetone for both fuels. The engine fueled with biodiesel emits a comparatively high content of propionaldehyde and methacrolein. Biodiesel, as an alternative fuel, has lower specific reactivity (SR) caused by carbonyls compared with diesel. When fueled with biodiesel, carbonyl compounds make more contribution to total hydrocarbon emission.

  12. Leaf level emissions of volatile organic compounds (VOC) from some Amazonian and Mediterranean plants

    NASA Astrophysics Data System (ADS)

    Bracho-Nunez, A.; Knothe, N. M.; Welter, S.; Staudt, M.; Costa, W. R.; Liberato, M. A. R.; Piedade, M. T. F.; Kesselmeier, J.

    2012-11-01

    As volatile organic compounds (VOCs) significantly affect atmospheric chemistry (oxidative capacity) and physics (secondary organic aerosol formation and effects), emission inventories defining regional and global biogenic VOC emission strengths are important. The aim of this work was to achieve a description of VOC emissions from poorly described tropical vegetation to be compared with the quite well investigated and highly heterogeneous emissions from Mediterranean vegetation. For this task, common plant species of both ecosystems were investigated. Sixteen plant species from the Mediterranean area, which is known for its special diversity in VOC emitting plant species, were chosen. In contrast, little information is currently available regarding emissions of VOCs from tropical tree species at the leaf level. Twelve plant species from different environments of the Amazon basin, i.e. Terra firme, Várzea and Igapó, were screened for emission of VOCs at leaf level with a branch enclosure system. Analysis of the volatile organics was performed online by a proton-transfer-reaction mass spectrometer (PTR-MS) and offline by collection on adsorbent tubes and subsequent gas chromatographic analysis. Isoprene was quantitatively the most dominant compound emitted followed by monoterpenes, methanol and acetone. Most of the Mediterranean species emitted a variety of monoterpenes, whereas only five tropical species were monoterpene emitters exhibiting a quite conservative emission pattern (α-pinene > limonene > sabinene > β-pinene). Mediterranean plants showed additional emissions of sesquiterpenes, whereas in the case of plants from the Amazon region no sesquiterpenes were detected probably due to a lack of sensitivity in the measuring systems. On the other hand methanol emissions, an indicator of growth, were common in most of the tropical and Mediterranean species. A few species from both ecosystems showed acetone emissions. The observed heterogeneous emissions

  13. A Global inventory of volatile organic compound emissions from anthropogenic sources

    NASA Astrophysics Data System (ADS)

    Piccot, Stephen D.; Watson, Joel J.; Jones, Julian W.

    1992-06-01

    As part of an effort to assess the potential impacts associated with global climate change, the U.S. Environmental Protection Agency's Office of Research and Development is supporting global atmospheric chemistry research by developing global scale estimates of volatile organic compound (VOC) emissions (excluding methane). Atmospheric chemistry models require, as one input, an emissions inventory of VOCs. Consequently, a global inventory of anthropogenic VOC emissions has been developed. The inventory includes VOC estimates for seven classes of VOCs: paraffins, olefins, aromatics (benzene, toluene, xylene), formaldehyde, other aldehydes, other aromatics, and marginally reactive compounds. These classes represent general classes of VOC compounds which possess different chemical reactivities in the atmosphere. The technical approach used to develop this inventory involved four major steps. The first step was to identify the major anthropogenic sources of VOC emissions in the United States and to group these sources into 28 general source groups. Source groups were developed to represent general categories such as "sources associated with oil and natural gas production" and more specific categories such as savanna buming. Emission factors for these source groups were then developed using different techniques and data bases. For example, emission factors for oil and natural gas production were estimated by dividing the United States' emissions from oil and gas production operations by the amount of oil and natural gas produced in the United States. Multiplication of these emission factors by production/consumption statistics for other countries yielded global VOC emission estimates for specific source groups within those countries. The final step in development of the VOC inventory was to distribute emissions into 10° by 10° grid cells using detailed maps of population and industrial activity. The results of this study show total global anthropogenic VOC emissions of

  14. The contribution of evaporative emissions from gasoline vehicles to the volatile organic compound inventory in Mexico City.

    PubMed

    Schifter, I; Díaz, L; Rodríguez, R; González-Macías, C

    2014-06-01

    The strategy for decreasing volatile organic compound emissions in Mexico has been focused much more on tailpipe emissions than on evaporative emissions, so there is very little information on the contribution of evaporative emissions to the total volatile organic compound inventory. We examined the magnitudes of exhaust and evaporative volatile organic compound emissions, and the species emitted, in a representative fleet of light-duty gasoline vehicles in the Metropolitan Area of Mexico City. The US "FTP-75" test protocol was used to estimate volatile organic compound emissions associated with diurnal evaporative losses, and when the engine is started and a journey begins. The amount and nature of the volatile organic compounds emitted under these conditions have not previously been accounted in the official inventory of the area. Evaporative emissions from light-duty vehicles in the Metropolitan Area of Mexico City were estimated to be 39 % of the total annual amount of hydrocarbons emitted. Vehicles built before 1992 (16 % of the fleet) were found to be responsible for 43 % of the total hydrocarbon emissions from exhausts and 31 % of the evaporative emissions of organic compounds. The relatively high amounts of volatile organic compounds emitted from older vehicles found in this study show that strong emission controls need to be implemented in order to decrease the contribution of evaporative emissions of this fraction of the fleet.

  15. Volatile organic compound emissions from elephant grass and bamboo cultivars used as potential bioethanol crop

    NASA Astrophysics Data System (ADS)

    Crespo, E.; Graus, M.; Gilman, J. B.; Lerner, B. M.; Fall, R.; Harren, F. J. M.; Warneke, C.

    2013-02-01

    Volatile organic compound (VOC) emissions from elephant grass (Miscanthus gigantus) and black bamboo (Phyllostachys nigra) were measured online in semi-field chamber and plant enclosure experiments during growth and harvest using proton-transfer reaction mass spectrometry (PTR-MS), proton-transfer reaction ion-trap mass spectrometry (PIT-MS) and gas chromatography-mass spectrometry (GC-MS). Both cultivars are being considered for second-generation biofuel production. Before this study, no information was available on their yearly VOC emissions. This exploratory investigation shows that black bamboo is a strong isoprene emitter (daytime 28,516 ng gdwt-1 h-1) and has larger VOC emissions, especially for wound compounds from the hexanal and hexenal families, than elephant grass. Daytime emissions of methanol, acetaldehyde, acetone + propanal and acetic acid of black bamboo were 618, 249, 351, and 1034 ng gdwt-1 h-1, respectively. In addition, it is observed that elephant grass VOC emissions after harvesting strongly depend on the seasonal stage. Not taking VOC emission variations throughout the season for annual and perennial species into account, may lead to an overestimation of the impact on local air quality in dry periods. In addition, our data suggest that the use of perennial grasses for extensive growing for biofuel production have lower emissions than woody species, which might be important for regional atmospheric chemistry.

  16. Leaf level emissions of volatile organic compounds (VOC) from some Amazonian and Mediterranean plants

    NASA Astrophysics Data System (ADS)

    Bracho-Nunez, A.; Knothe, , N. M.; Welter, S.; Staudt, M.; Costa, W. R.; Liberato, M. A. R.; Piedade, M. T. F.; Kesselmeier, J.

    2013-09-01

    Emission inventories defining regional and global biogenic volatile organic compounds (VOC) emission strengths are needed to determine the impact of VOC on atmospheric chemistry (oxidative capacity) and physics (secondary organic aerosol formation and effects). The aim of this work was to contribute with measurements of tree species from the poorly described tropical vegetation in direct comparison with the quite well-investigated, highly heterogeneous emissions from Mediterranean vegetation. VOC emission from sixteen plant species from the Mediterranean area were compared with twelve plant species from different environments of the Amazon basin by an emission screening at leaf level using branch enclosures. Analysis of the volatile organics was performed online by a proton-transfer-reaction mass spectrometer (PTR-MS) and offline by collection on adsorbent tubes and subsequent gas chromatographic analysis. Isoprene was the most dominant compound emitted followed by monoterpenes, methanol and acetone. The average loss rates of VOC carbon in relation to the net CO2 assimilation were found below 4% and indicating normal unstressed plant behavior. Most of the Mediterranean species emitted a large variety of monoterpenes, whereas only five tropical species were identified as monoterpene emitters exhibiting a quite conservative emission pattern (α-pinene < limonene < sabinene < ß-pinene). Mediterranean plants showed additional emissions of sesquiterpenes. In the case of Amazonian plants no sesquiterpenes were detected. However, missing of sesquiterpenes may also be due to a lack of sensitivity of the measuring systems. Furthermore, our screening activities cover only 1% of tree species of such tropical areas as estimated based on recent biodiversity reports. Methanol emissions, an indicator of growth, were found to be common in most of the tropical and Mediterranean species. A few species from both ecosystems showed acetone emissions. The observed heterogeneous

  17. Cold Temperature and Biodiesel Fuel Effects on Speciated Emissions of Volatile Organic Compounds from Diesel Trucks

    EPA Science Inventory

    Speciated volatile organic compounds (VOCs) were measured in diesel exhaust from three medium heavy-duty trucks equipped with modern aftertreatment technologies. Emissions testing was conducted on a chassis dynamometer at two ambient temperatures (-6.7°C and 21.7°C) operating on ...

  18. Modeling emissions of volatile organic compounds from silage storages and feed lanes

    Technology Transfer Automated Retrieval System (TEKTRAN)

    An initial volatile organic compound (VOC) emission model for silage sources, developed using experimental data from previous studies, was incorporated into the Integrated Farm System Model (IFSM), a whole-farm simulation model used to assess the performance, environmental impacts, and economics of ...

  19. Emission of volatile organic compounds as affected by rate of application of cattle manure

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Beef cattle manure can serve as a valuable nutrient source for crop production. However, emissions of volatile organic compounds (VOCs) following land application may pose a potential off-site odor concern. This study was conducted to evaluate the effects of land application method, N- application...

  20. Emission of volatile organic compounds after land application of cattle manure

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Beef cattle manure can serve as a valuable source of nutrients for crop production. However, emissions of volatile organic compounds (VOCs) following land application may pose an odor nuisance to downwind populations. This study was conducted to evaluate the effects of application method, diet, so...

  1. Microbial Volatile Organic Compound Emissions from Stachybotrys chartarum growing on Gypsum Wallboard and Ceiling tile

    EPA Science Inventory

    This study compared seven toxigenic strains of S. chartarum found in water-damaged buildings to characterize the microbial volatile organic compound (MVOC) emissions profile while growing on gypsum wallboard (W) and ceiling tile (C) coupons. The inoculated coupons with their sub...

  2. BIOGENIC VOLATILE ORGANIC COMPOUND EMISSIONS FROM DESERT VEGETATION OF THE SOUTHWESTERN U.S.

    EPA Science Inventory

    Thirteen common plant species in the Mojave and Sonoran Desert regions of the western United States were tested for emissions of biogenic non-methane volatile organic compounds (BVOCs). Only two of the species examined emitted isoprene at rates of 10 µgCg−1 ...

  3. BIOGENIC VOLATILE ORGANIC COMPOUND EMISSIONS FROM A LOWLAND TROPICAL WET FOREST IN COSTA RICA

    EPA Science Inventory

    Twenty common plant species were screened for emissions of biogenic volatile organic compounds (BVOCS) at a lowland tropical wet forest site in Costa Rica. Ten of the species. examined emitted substantial quantities of isoprene. These species accounted for 35-50% of the total bas...

  4. 76 FR 74014 - Approval and Promulgation of Implementation Plans; Illinois; Volatile Organic Compound Emission...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-11-30

    ... Compound Emission Control Measures for Chicago and Metro-East St. Louis Ozone Nonattainment Areas AGENCY: Environmental Protection Agency (EPA). ACTION: Proposed rule. SUMMARY: On July 29, 2010, September 16, 2011, and September 29, 2011, the Illinois Environmental Protection Agency (IEPA) submitted several volatile...

  5. Volatile organic compound analysis in wood combustion and meat cooking emissions

    SciTech Connect

    Zielinska, B.; McDonald, J.

    1999-07-01

    Residential wood combustion and meat cooking emissions were each analyzed for volatile organic compounds (VOC). Emissions were diluted 60--100 times, cooled to ambient temperature, and allowed 80 seconds for condensation prior to collection with the aid of a DRI-constructed dilution stack sampler. Fireplace and wood-stove emissions testing was conducted at the DRI facilities. Wood type, wood moisture, burn rate, and fuel load were varied for different experiments. Meat emissions testing was conducted at the CE-CERT stationary emissions lab, University of California, Riverside. Meat type, fat content, and cooking appliance were changed in different tests. VOCs were collected using stainless-steel 6 L canisters and Tenax cartridges, whereas for carbonyl compound collection 2,4-dinitrophenylhydrazine (DNPH)-impregnated C{sub 18} SepPack cartridges were used. Analysis of VOC collected with canisters and Tenax cartridges was conducted by Gas Chromatography/Mass Spectrometry (GC/MS) and by GC/FID/ECD (flame ionization detection/electron capture detection). DNPH-impregnated cartridges were analyzed for fourteen C{sub 1}--C{sub 7} carbonyl compounds, using the HPLC method. The results of these measurements are discussed.

  6. Volatile compounds emission from canopy fine litterfall in a hemiboreal mixed forest at Järvselja

    NASA Astrophysics Data System (ADS)

    Portillo-Estrada, Miguel; Noe, Beate; Noe, Steffen M.

    2013-04-01

    The seasonal distribution of biogenic volatile organic compounds (BVOC) emissions from canopy fine litterfall was investigated over a period of two years. Three stands of a hemiboreal mixed forest were studied. The stands presented different dominant tree species: (1) Norway spruce, (2) Scots pine, and (3) Silver birch and Downy birch. The litterfall was monthly collected in litter traps. The BVOC emission of litter was sampled by placing the litter into a glass jar equipped with a vent tube and pumping the head space air through a VOC adsorbing tube (carbotrap). Adsorbed BVOCs were analyzed in a GC-MS. Fifteen compounds were quantified. Seasonal differences in the total emission of BVOCs were found, defined by a maximum in summer and a minimum in autumn and winter. During summer months, litter emissions were dominated by limonene, α-pinene, camphene and 3-carene in the three litter types, accounting for 70-75 % of total BVOC emitted in June. 3-Carene, α-pinene and β-pinene were the main compounds emitted during winter time, accounting for 50-60 % of total BVOC emitted in January. Stand to stand differences were assessed. The spruce and birch dominated stands showed more similarities in their BVOC emission pattern if compared to the pine dominated stand. Together with the litterfall data, an estimation of the annual total BVOC emitted by the soil litter layer is presented for each stand type.

  7. Flooding induced emissions of volatile signalling compounds in three tree species with differing waterlogging tolerance.

    PubMed

    Copolovici, Lucian; Niinemets, Ulo

    2010-09-01

    To gain insight into variations in waterlogging responsiveness, net assimilation rate, stomatal conductance, emissions of isoprene and marker compounds of anoxic metabolism ethanol and acetaldehyde, and stress marker compounds nitric oxide (NO), volatile products of lipoxygenase (LOX) pathway and methanol were studied in seedlings of temperate deciduous tree species Alnus glutinosa, Populus tremula and Quercus rubra (from highest to lowest waterlogging tolerance) throughout sustained root zone waterlogging of up to three weeks. In all species, waterlogging initially resulted in reductions in net assimilation and stomatal conductance and enhanced emissions of ethanol, acetaldehyde, NO, LOX products and methanol, followed by full or partial recovery depending on process and species. Strong negative correlations between g(s) and internal NO concentration and NO flux, valid within and across species, were observed throughout the experiment. Isoprene emission capacity was not related to waterlogging tolerance. Less waterlogging tolerant species had greater reduction and smaller acclimation capacity in foliage physiological potentials, and larger emission bursts of volatile stress marker compounds. These data collectively provide encouraging evidence that emissions of volatile organics and NO can be used as quantitative measures of stress tolerance and acclimation kinetics in temperate trees.

  8. Emission control of sodium compounds and their formation mechanisms during coal combustion

    SciTech Connect

    Tsuyoshi Takuwa; Ichiro Naruse

    2007-07-01

    In order to control emissions of sodium compounds during coal combustion, the sorbent injection technology is tested during coal combustion. Kaolin is selected as the sorbent to absorb vapors of sodium compounds evolved from the coals. In the combustion experiments, the kaolin is physically mixed with coal. Two types of coal, which have the similar coal properties, are burned. Combustion tests are conducted, using an electrically heated drop tube furnace, to study effect of kaolin addition on the capture characteristics of sodium compounds. In order to elucidate fundamentals on transformation behaviors of sodium compounds during hydrogen-air combustion, chemical kinetic simulation by elementary reactions relating to sodium compounds is also performed, varying the reaction atmosphere. As a result, the kaolin can effectively capture the vapor of sodium compounds even during coal combustion. The capture efficiency depends on the coal type. The sodium compounds for the coals, which produce many fine particles with size of less than 1 {mu}m, tend to be effectively captured by the kaolin. According to the kinetic simulation of sodium species, difference of the reaction atmosphere affects occurrence species of sodium vapor. In the combustion region, the sodium compounds become metallic sodium vapor in any reaction atmospheres due to occurrence of the reducing radical species. HCl gas rather than SO{sub 2} gas plays an important role to transform gaseous sodium compounds. 44 refs., 8 figs., 3 tabs.

  9. Emissions of carbon species, organic polar compounds, potassium, and mercury from prescribed burning activities

    NASA Astrophysics Data System (ADS)

    Zhang, Y.; Obrist, D.; Zielinska, B.; Gerler, A.

    2012-04-01

    Biomass burning is an important emission source of pollutants to the atmosphere, but few studies have focused on the chemical composition of emissions from prescribed burning activities. Here we present results from a sampling campaign to quantify particulate-phase emissions from various types of prescribed fires including carbon species (Elemental Carbon: EC; Organic Carbon: OC; and Total Carbon: TC); polar organic compounds (12 different compounds and four functional classes); water-soluble potassium (K+); and mercury (Hg). We measured emissions from the following types of prescribed biomass burning in the Lake Tahoe basin located on the California/Nevada border: (i) log piles stacked and dried in the field; (ii) log piles along with green understory vegetation; and (iii) understory green vegetation and surface litter; further emissions were collected from burns conducted in a wood stove: (iv) dried wooden logs; (v) green foliage of understory vegetation collected from the field; and (vi) surface organic litter collected from the field; finally, samples were also taken from (vii) ambient air in residential areas during peak domestic wood combustion season. Results show that OC/EC ratios of prescribed burns in the field ranged from 4 to 10, but lower values (around 1) were observed in controlled stove fires. These results are consistent with an excess of OC emissions over EC found in wildfires. OC/EC ratios, however, showed clear separations between controlled wood stove combustion (higher EC) and prescribed burns in the field (lower EC). We attribute this difference to a higher combustion temperatures and dominance of flaming combustion in wood stove fires. OC positively and linearly correlated to the sum of polar organic compounds across all burn types (r2 of 0.82). The most prevalent group of polar compounds emitted during prescribed fires was resin acids (dehydroabietic, pimaric, and abietic acids), followed by levoglucosan plus mannositol. Negligible

  10. Production of extremely low volatile organic compounds from biogenic emissions: Measured yields and atmospheric implications

    SciTech Connect

    Jokinen, Tuija; Berndt, Torsten; Makkonen, Risto; Kerminen, Veli-Matti; Junninen, Heikki; Paasonen, Pauli; Stratmann, Frank; Herrmann, Hartmut; Guenther, Alex B.; Worsnop, Douglas R.; Kulmala, M.; Ehn, Mikael K.; Sipila, Mikko

    2015-06-09

    Extremely low volatility organic compounds (ELVOC) are suggested to promote aerosol particle formation and cloud condensation nuclei (CCN) production in the atmosphere. We show that the capability of biogenic VOC (BVOC) to produce ELVOC depends strongly on their chemical structure and relative oxidant levels. BVOC with an endocyclic double bond, representative emissions from, e.g., boreal forests, efficiently produce ELVOC from ozonolysis. Compounds with exocyclic double bonds or acyclic compounds including isoprene, emission representative of the tropics, produce minor quantities of ELVOC, and the role of OH radical oxidation is relatively larger. Implementing these findings into a global modeling framework shows that detailed assessment of ELVOC production pathways is crucial for understanding biogenic secondary organic aerosol and atmospheric CCN formation.

  11. Characteristics of volatile organic compounds (VOCs) from the evaporative emissions of modern passenger cars

    NASA Astrophysics Data System (ADS)

    Yue, Tingting; Yue, Xin; Chai, Fahe; Hu, Jingnan; Lai, Yitu; He, Liqang; Zhu, Rencheng

    2017-02-01

    Volatile organic compounds (VOCs) from vehicle evaporative emissions contribute substantially to photochemical air pollution. Yet, few studies of the characteristics of VOCs emitted from vehicle evaporative emissions have been published. We investigate the characteristics of 57 VOCs in hot soak, 24 h diurnal and 48 h diurnal emissions by applying the Sealed Housing Evaporative Determination unit (SHED) test to three modern passenger cars (one US Tier 2 and two China IV vehicles) using two different types of gasoline. The characteristics of the VOCs from the hot soak, 24 h diurnal and 48 h diurnal emissions were different due to their different emission mechanisms. In the hot soak emissions, toluene, isopentane/n-pentane, and 2,2,4-trimethylpentane were dominant species. In the 24 h and 48 h diurnal emissions, isopentane and n-pentane were dominant species. Toluene was the third most dominant component in the 24 h diurnal emissions but decreased by a mass of 42%-80% in the 48 h diurnal emissions. In the hot soak, 24 h diurnal and 48 h diurnal emissions, alkanes were generally the dominant hydrocarbons, followed by aromatics and olefins. However, owing to different evaporative emission mechanisms, the weight percentages of the aromatic hydrocarbons decreased and the weight percentages of the alkanes increased from the hot soak test to the 24 h diurnal and 48 h diurnal tests for each vehicle. The dominant contributors to the ozone formation potentials (OFPs) were also different in the hot soak, 24 h diurnal and 48 h diurnal emissions. The OFPs (g O3/g VOC) of the hot soak emissions were higher than those of the 24 h and 48 h diurnal emissions. In addition, the combined effect of decreasing the olefin and aromatic contents of gasoline on vehicle evaporative emissions was investigated. The aromatics all decreased substantially in the hot soak, 24 h and 48 h diurnal emissions, and the total masses of the VOCs and OFPs decreased, with the greatest reduction occurring in

  12. Doubled volatile organic compound emissions from subarctic tundra under simulated climate warming.

    PubMed

    Faubert, Patrick; Tiiva, Päivi; Rinnan, Asmund; Michelsen, Anders; Holopainen, Jarmo K; Rinnan, Riikka

    2010-07-01

    *Biogenic volatile organic compound (BVOC) emissions from arctic ecosystems are important in view of their role in global atmospheric chemistry and unknown feedbacks to global warming. These cold ecosystems are hotspots of climate warming, which will be more severe here than averaged over the globe. We assess the effects of climatic warming on non-methane BVOC emissions from a subarctic heath. *We performed ecosystem-based chamber measurements and gas chromatography-mass spectrometry (GC-MS) analyses of the BVOCs collected on adsorbent over two growing seasons at a wet subarctic tundra heath hosting a long-term warming and mountain birch (Betula pubescens ssp. czerepanovii) litter addition experiment. *The relatively low emissions of monoterpenes and sesquiterpenes were doubled in response to an air temperature increment of only 1.9-2.5 degrees C, while litter addition had a minor influence. BVOC emissions were seasonal, and warming combined with litter addition triggered emissions of specific compounds. *The unexpectedly high rate of release of BVOCs measured in this conservative warming scenario is far above the estimates produced by the current models, which underlines the importance of a focus on BVOC emissions during climate change. The observed changes have implications for ecological interactions and feedback effects on climate change via impacts on aerosol formation and indirect greenhouse effects.

  13. Diurnal and seasonal emissions of volatile organic compounds from cork oak ( Quercus suber) trees

    NASA Astrophysics Data System (ADS)

    Pio, C. A.; Silva, P. A.; Cerqueira, M. A.; Nunes, T. V.

    The emissions of volatile organic compounds from Quercus suber (cork oak) were investigated at two rural sites in Portugal using a branch enclosure method with subsequent analysis by gas chromatography/flame ionization detection. Q. suber leaves released important amounts of monoterpenes, mainly in the form of limonene, α-pinene, β-pinene and sabinene. However, significant temporal and intraspecific variations in the relative abundance of the dominant compounds were found during this survey. Emissions from Q. suber were strongly dependent on light and temperature, showing a similar behaviour to that of plant species known to be isoprene producers. But, this work also revealed that, although at lower rates, emissions of monoterpenes continued in the dark for several hours. Emission rates were quite well predicted by algorithms based on the Guenther and Tingey equations; correlations of measurements with modelled data were, on average, r2=0.80. A pronounced seasonal variation was recorded for the emissions of monoterpenes. During the 1-yr study period, standard emission rates ranged between a minimum of 0.2 μg g dw-1 h -1, in winter, and a maximum of 20-30 μg g dw-1 h -1, in summer.

  14. Biogenic volatile organic compound emissions along a high arctic soil moisture gradient.

    PubMed

    Svendsen, Sarah Hagel; Lindwall, Frida; Michelsen, Anders; Rinnan, Riikka

    2016-12-15

    Emissions of biogenic volatile organic compounds (BVOCs) from terrestrial ecosystems are important for the atmospheric chemistry and the formation of secondary organic aerosols, and may therefore influence the climate. Global warming is predicted to change patterns in precipitation and plant species compositions, especially in arctic regions where the temperature increase will be most pronounced. These changes are potentially highly important for the BVOC emissions but studies investigating the effects are lacking. The aim of this study was to investigate the quality and quantity of BVOC emissions from a high arctic soil moisture gradient extending from dry tundra to a wet fen. Ecosystem BVOC emissions were sampled five times in the July-August period using a push-pull enclosure technique, and BVOCs trapped in absorbent cartridges were analyzed using gas chromatography-mass spectrometry. Plant species compositions were estimated using the point intercept method. In order to take into account important underlying ecosystem processes, gross ecosystem production, ecosystem respiration and net ecosystem production were measured in connection with chamber-based BVOC measurements. Highest emissions of BVOCs were found from vegetation communities dominated by Salix arctica and Cassiope tetragona, which had emission profiles dominated by isoprene and monoterpenes, respectively. These results show that emissions of BVOCs are highly dependent on the plant cover supported by the varying soil moisture, suggesting that high arctic BVOC emissions may affect the climate differently if soil water content and plant cover change.

  15. Diurnal and seasonal variability of gasoline-related volatile organic compound emissions in Riverside, California.

    PubMed

    Gentner, Drew R; Harley, Robert A; Miller, Angela M; Goldstein, Allen H

    2009-06-15

    On- and off-road mobile sources are the dominant contributors to urban anthropogenic volatile organic compound (AVOC) emissions. Analyses of gasoline samples from California for both summer and winter indicate significant differences in liquid fuel and vapor chemical composition due to intentional seasonal adjustments. Ambient concentrations of 55 VOCs were measured via in situ gas chromatography in the 2005 Study of Organic Aerosols at Riverside (SOAR) during both summer and fall. A chemical mass balance analysis was used to differentiate vapor pressure-driven VOC emissions from other motor vehicle-related emissions such as tailpipe exhaust. Overall, fuel vapor emissions accounted for 31 +/- 2% of gasoline-related VOC in Riverside; California's emission factor model similarly estimates 31% of gasoline-related VOC emissions are fuel vapor. The diurnal pattern of vapor pressure-driven VOC source contributions is relatively stable around 10 microg/m3, while whole gasoline (i.e., tailpipe) contributions peak at approximately 60 microg/m3 during the morning commute. There is no peak in whole gasoline source contributions during the afternoon, due to rapid dilution associated with high mixing heights and wind speeds in the Riverside area. The relationship between estimated gasoline-related VOC and observed carbon monoxide concentrations in this study is similar to California's 2005 emission inventory; we calculated a VOC to CO mass ratio of 0.086 +/- 0.006 (95% CI) compared to 0.097 in the emission inventory for all gasoline-related sources.

  16. Emission of volatile organic compounds (VOC) from tropical plant species in India.

    PubMed

    Padhy, P K; Varshney, C K

    2005-06-01

    Foliar emission of volatile organic compounds (VOC) from common Indian plant species was measured. Dynamic flow enclosure technique was used and the gas samples were collected onto Tenax-GC/Carboseive cartridges. The Tenax-GC/Carboseive cartridges were attached to the thermal disorber sample injection system and the gas sample was analysed using gas chromatography (GC) with flame ionisation detection (FID). Fifty-one local plant species were screened, out of which 36 species were found to emit VOC (4 high emitter; 28 moderate emitter; and 4 low-emitter), while in the remaining 15 species no VOC emission was detected or the levels of emission were below detection limit (BDL). VOC emission was found to vary from one species to another. There was a marked seasonal and diurnal variation in VOC emission. The minimum and maximum VOC emission values were < 0.1 and 87 microgg(-1) dry leaf h(-1) in Ficus infectoria and Lantana camara respectively. Out of the 51 plant species studied, 13 species are reported here for the first time. Among the nine tree species (which were selected for detailed study), the highest average hourly emission (9.69+/-8.39 microgg(-1) dry leaf) was observed in Eucalyptus species and the minimum in Syzygium jambolanum (1.89+/-2.48 microgg(-1) dry leaf). An attempt has been made to compare VOC emission from different plant species between present study and the literature (tropical and other regions).

  17. Existing Pittsburgh Compound-B positron emission tomography thresholds are too high: statistical and pathological evaluation.

    PubMed

    Villeneuve, Sylvia; Rabinovici, Gil D; Cohn-Sheehy, Brendan I; Madison, Cindee; Ayakta, Nagehan; Ghosh, Pia M; La Joie, Renaud; Arthur-Bentil, Samia Kate; Vogel, Jacob W; Marks, Shawn M; Lehmann, Manja; Rosen, Howard J; Reed, Bruce; Olichney, John; Boxer, Adam L; Miller, Bruce L; Borys, Ewa; Jin, Lee-Way; Huang, Eric J; Grinberg, Lea T; DeCarli, Charles; Seeley, William W; Jagust, William

    2015-07-01

    Amyloid-β, a hallmark of Alzheimer's disease, begins accumulating up to two decades before the onset of dementia, and can be detected in vivo applying amyloid-β positron emission tomography tracers such as carbon-11-labelled Pittsburgh compound-B. A variety of thresholds have been applied in the literature to define Pittsburgh compound-B positron emission tomography positivity, but the ability of these thresholds to detect early amyloid-β deposition is unknown, and validation studies comparing Pittsburgh compound-B thresholds to post-mortem amyloid burden are lacking. In this study we first derived thresholds for amyloid positron emission tomography positivity using Pittsburgh compound-B positron emission tomography in 154 cognitively normal older adults with four complementary approaches: (i) reference values from a young control group aged between 20 and 30 years; (ii) a Gaussian mixture model that assigned each subject a probability of being amyloid-β-positive or amyloid-β-negative based on Pittsburgh compound-B index uptake; (iii) a k-means cluster approach that clustered subjects into amyloid-β-positive or amyloid-β-negative based on Pittsburgh compound-B uptake in different brain regions (features); and (iv) an iterative voxel-based analysis that further explored the spatial pattern of early amyloid-β positron emission tomography signal. Next, we tested the sensitivity and specificity of the derived thresholds in 50 individuals who underwent Pittsburgh compound-B positron emission tomography during life and brain autopsy (mean time positron emission tomography to autopsy 3.1 ± 1.8 years). Amyloid at autopsy was classified using Consortium to Establish a Registry for Alzheimer's Disease (CERAD) criteria, unadjusted for age. The analytic approaches yielded low thresholds (standard uptake value ratiolow = 1.21, distribution volume ratiolow = 1.08) that represent the earliest detectable Pittsburgh compound-B signal, as well as high thresholds (standard

  18. [Study on volatile organic compounds emission of straw combustion and management countermeasure in Wuhan city].

    PubMed

    Huang, Bi-Jie

    2013-12-01

    Straw combustion is an important anthropogenic source of volatile organic compounds (VOCs) in China. Emissions of VOCs from straw combustion significantly affect climate forcing and human health. A reliable estimation of VOCs emission from the source is the important prerequisite for emission impact assessment and control strategy in the urban or regional areas. VOCs emissions from straw combustion in Wuhan City and the districts were estimated by factor analysis method, which was based on the yield of major farm crops in the period of 2005-2011. Moreover, Cultivated-land Emission Intensity (Ie) and Regional Emission Intensity (Ir) were also calculated. VOCs Emissions from straw combustion in Wuhan City were (3,163 +/- 139) t in the period of 2005-2011; Ie and Ir was (1.52 +/- 0.06) t x km(-2) and (0.37 +/- 0.02) t x km(-2), respectively; Straw combustion of grain and oilseed crops was the main source of the emissions; 21 kinds of VOCs should be listed as the priority control pollutants for straw combustion in Wuhan City. The order of successively decreasing VOCs emission of districts in Wuhan City was Huangpi District, Xinzhou District, Jiangxia District, Caidian District, Hannan District, and Dongxihu District, the former 4 districts contributed to almost 90% VOCs emissions of the Wuhan City. Huangpi District, Xinzhou District, Jiangxia District, and Hannan District should be regarded as priority control areas of VOCs emission from straw combustion in Wuhan City. Much attention should be paid to Jiangxia District, which was nationally representative. Ie and Ir are important basic data for ecological risk assessment of some kind of pollutants emitted from straw combustion in the urban or regional areas. Furthermore, straw utilization model according to agricultural cyclic economy is a feasible way to cope with the environmental problem of straw combustion.

  19. Large drought-induced variations in oak leaf volatile organic compound emissions during PINOT NOIR 2012

    DOE PAGES

    Geron, Chris; Gu, Lianhong; Daly, Ryan; ...

    2015-12-17

    Here, leaf-level isoprene and monoterpene emissions were collected and analyzed from five of the most abundant oak (Quercus) species in Central Missouri's Ozarks Region in 2012 during PINOT NOIR (Particle Investigations at a Northern Ozarks Tower – NOx, Oxidants, Isoprene Research). June measurements, prior to the onset of severe drought, showed isoprene emission rates and leaf temperature responses similar to those previously reported in the literature and used in Biogenic Volatile Organic Compound (BVOC) emission models. During the peak of the drought in August, isoprene emission rates were substantially reduced, and response to temperature was dramatically altered, especially for themore » species in the red oak subgenus (Erythrobalanus).« less

  20. Emission of reactive compounds and secondary products from wood-based furniture coatings

    NASA Astrophysics Data System (ADS)

    Salthammer, T.; Schwarz, A.; Fuhrmann, F.

    Emissions of organic fragmentation products, so-called "secondary emission products" and reactive species from wood-based furniture coatings have been studied in 1 m 3 test chambers. the climatic conditions were representative of indoor environments. Relevant compounds and compound groups were the wetting agent 2,4,7,9-tetramethyl-5-dicyne-4,7-diol (T4MDD), the plasticiser di-2-ethyl-hexyl-phthalate (DEHP), aliphatic aldehydes, monoterpenes, photoinitiator fragments, acrylic monomers/reactive solvents and diisocyanate monomers. Such substances may affect human health in several ways. Aliphatic aldehydes and some photoinitiator fragments are of strong odour, while acrylates and diisocyanates cause irritation of skin, eyes and upper airways. Terpenes and reactive solvents like styrene undergo indoor chemistry in the presence of ozone, nitrogen oxides or hydroxy radicals. Secondary emission products and reactive species can achieve significant indoor concentrations. On the other hand, it has been reported that even small quantities can cause health effects. In the cases of indoor studies with special regard to emissions from furniture, chemical analysis should always include these compounds.

  1. Speciated non-methane organic compounds emissions from food cooking in Mexico

    NASA Astrophysics Data System (ADS)

    Mugica, V.; Vega, E.; Chow, J.; Reyes, E.; Sánchez, G.; Arriaga, J.; Egami, R.; Watson, J.

    Non-methane organic compound (NMOC) emissions from different sorts of food preparation sites, were quantified for the first time in Mexico, in order to develop emission profiles for further application in the chemical mass balance receptor model (CMB). Restaurants using charcoal grills and LP gas stoves, "tortillerı´as", food frying places and rotisseries were sampled using SUMMA ® stainless-steel canisters to analyse NMOC by high-resolution gas chromatography. The results obtained show that profiles determined from food cooking processes have similarities to those found in LP gas combustion, which is the most common fuel in Mexico used for this purpose, although there were differences in the relative composition of propane and butane in both cases. This suggests that, the rates of combustion of propane and butane are different. It has also been detected that propene, a reactive olefin is produced during the combustion process. The obtained profiles of restaurants, rotisseries and fried food show an important contribution of two carbon compounds (ethane, ethylene and acetylene) that can be attributed to the complex process of grease and meat cooking. The presence of these compounds cannot be attributed to vehicular sources since the concentrations are higher than in ambient air. These were also determined from aromatic compounds such as benzene, toluene and xylene in the combustion of vegetal charcoal. The measured concentrations indicate that NMOC emissions from cooking may become an important indoor source of NMOC under crowded conditions in closed places.

  2. Monoterpene emissions and carbonyl compound air concentrations during the blooming period of rape (Brassica napus).

    PubMed

    Müller, Konrad; Pelzing, Matthias; Gnauk, Thomas; Kappe, Anett; Teichmann, Ulrich; Spindler, Gerald; Haferkorn, Sylvia; Jahn, Yvonne; Herrmann, Hartmut

    2002-12-01

    An increasing percentage of agricultural land in Germany is used for oil seed plants. Hence, rape has become an important agricultural plant (in Saxony 1998: 12% of the farmland) in the recent years. During flowering of rape along with intensive radiation and high temperatures, a higher production and emission of biogenic VOC was observed. The emissions of terpenes were determined and more importantly, high concentrations of organic carbonyl compounds were observed during this field experiment. All measurements of interest have been carried out during two selected days with optimal weather conditions. It is found that the origin or the mechanism of formation of different group of compounds had strong influence on the day to day variation of their concentrations. The emission flux of terpenes from flowering rape plants was determined to be 16-32 microg h(-1) m(-2) (30-60 ng h(-1) per g dry plant-540-11080 ng h(-1) per plant), in total. Limonene, alpha-thujene and sabinene were the most important compounds (about 60% of total terpenes). For limonene and sabinene reference emission rates (Ms) and temperature coefficients were determined: beta(limonene) = 0.108 K(-1) and Ms = 14.57 microg h(-1) m(-2) beta(sabinene) = 0.095 K(-1) and Ms = 5.39 microg h(-1) m(-2). The detected carbonyl compound concentrations were unexpectedly high (maximum formaldehyde concentration was 18.1 ppbv and 3.4 ppbv for butyraldehyde) for an open field. Possible reasons for these concentrations are the combination of primary emission from the plants induced by high temperature and high ozone stress, the secondary formation from biogenically and advected anthropogenically emitted VOC at high radiation intensities and furthered by the low wind speeds at this time.

  3. Contribution of flowering trees to urban atmospheric biogenic volatile organic compound emissions

    NASA Astrophysics Data System (ADS)

    Baghi, R.; Helmig, D.; Guenther, A.; Duhl, T.; Daly, R.

    2012-10-01

    Emissions of biogenic volatile organic compounds (BVOC) from urban trees during and after blooming were measured during spring and early summer 2009 in Boulder, Colorado. Air samples were collected onto solid adsorbent cartridges from branch enclosures on the tree species crabapple (Malus sp.), horse chestnut (Aesculus carnea, "Ft. McNair"), honey locust (Gleditsia triacanthos, "Sunburst"), and hawthorn (Crataegus laevigata, "Pauls Scarlet"). These species constitute ~ 65% of the insect-pollinated fraction of the flowering tree canopy (excluding catkin-producing trees) from the street area managed by the City of Boulder. Samples were analyzed for C10-C15 BVOC by thermal desorption and gas chromatography coupled to a flame ionization detector and a mass spectrometer (GC/FID/MS). Identified emissions and emission rates from these four tree species during the flowering phase were found to vary over a wide range. Monoterpene emissions were identified for honey locust, horse chestnut and hawthorn. Sesquiterpene emissions were observed in horse chestnut and hawthorn samples. Crabapple flowers were found to emit significant amounts of benzyl alcohol and benzaldehyde. Floral BVOC emissions increased with temperature, generally exhibiting exponential temperature dependence. Changes in BVOC speciation during and after the flowering period were observed for every tree studied. Emission rates were significantly higher during the blooming compared to the post-blooming state for crabapple and honey locust. The results were scaled to the dry mass of leaves and flowers contained in the enclosure. Only flower dry mass was accounted for crabapple emission rates as leaves appeared at the end of the flowering period. Total normalized (30 °C) monoterpene emissions from honey locust were higher during flowering (5.3 μgC g-1 h-1) than after flowering (1.2 μgC g-1 h-1). The total normalized BVOC emission rate from crabapple (93 μgC g-1 h-1) during the flowering period is of the same

  4. Assessing methods to estimate emissions of non-methane organic compounds from landfills.

    PubMed

    Saquing, Jovita M; Chanton, Jeffrey P; Yazdani, Ramin; Barlaz, Morton A; Scheutz, Charlotte; Blake, Don R; Imhoff, Paul T

    2014-11-01

    The non-methane organic compound (NMOC) emission rate is used to assess compliance with landfill gas emission regulations by the United States Environmental Protection Agency (USEPA). A recent USEPA Report (EPA/600/R-11/033) employed a ratio method to estimate speciated NMOC emissions (i.e., individual NMOC emissions): speciated NMOC emissions=measured methane (CH4) emission multiplied by the ratio of individual NMOCs concentration relative to CH4 concentration (C(NMOCs)/C(CH4)) in the landfill header gas. The objectives of this study were to (1) evaluate the efficacy of the ratio method in estimating speciated NMOC flux from landfills; (2) determine for what types of landfills the ratio method may be in error and why, using recent field data to quantify the spatial variation of (C(NMOCs)/C(CH4)) in landfills; and (3) formulate alternative models for estimating NMOC emissions from landfills for cases in which the ratio method results in biased estimates. This study focuses on emissions through landfill covers measured with flux chambers and evaluates the utility of the ratio method for estimating NMOC emission through this pathway. Evaluation of the ratio method was performed using CH4 and speciated NMOC concentration and flux data from 2012/2013 field sampling of four landfills, an unpublished landfill study, and literature data from three landfills. The ratio method worked well for landfills with thin covers (<40 cm), predicting composite NMOC flux (as hexane-C) to within a factor of 10× for 13 out of 15 measurements. However, for thick covers (⩾40 cm) the ratio method overestimated NMOC emissions by ⩾10× for 8 out of 10 measurements. Alternative models were explored incorporating other chemical properties into the ratio method. A molecular weight squared (MW)(2)-modified ratio equation was shown to best address the tendency of the current ratio method to overestimate NMOC fluxes for thick covers. While these analyses were only performed using NMOC fluxes

  5. Impacts of global emissions of CO, NO x , and CH4 on China tropospheric hydroxyl free radicals

    NASA Astrophysics Data System (ADS)

    Su, Mingfeng; Lin, Yunping; Fan, Xinqiang; Peng, Li; Zhao, Chunsheng

    2012-07-01

    Using the global chemistry and transport model MOZART, the simulated distributions of tropospheric hydroxyl free radicals (OH) over China and its sensitivities to global emissions of carbon monoxide (CO), nitrogen oxide (NO x ), and methane (CH4) were investigated in this study. Due to various distributions of OH sources and sinks, the concentrations of tropospheric OH in east China are much greater than in west China. The contribution of NO + perhydroxyl radical (HO2) reaction to OH production in east China is more pronounced than that in west China, and because of the higher reaction activity of non-methane volatile organic compounds (NMVOCs), the contributions to OH loss by NMVOCs exceed those of CO and take the dominant position in summer. The results of the sensitivity runs show a significant increase of tropospheric OH in east China from 1990 to 2000, and the trend continues. The positive effect of double emissions of NO x on OH is partly offset by the contrary effect of increased CO and CH4 emissions: the double emissions of NO x will cause an increase of OH of 18.1%-30.1%, while the increases of CO and CH4 will cause a decrease of OH of 12.2%-20.8% and 0.3%-3.0%, respectively. In turn, the lifetimes of CH4, CO, and NO x will increase by 0.3%-3.1% with regard to double emissions of CH4, 13.9%-26.3% to double emissions of CO and decrease by 15.3%-23.2% to double emissions of NO x .

  6. Thermogenic respiratory processes drive the exponential increase of volatile organic compound emissions in Macrozamia cycad cones.

    PubMed

    Terry, L Irene; Roemer, Robert B; Booth, David T; Moore, Chris J; Walter, Gimme H

    2016-07-01

    An important outcome of plant thermogenesis is increased emissions of volatiles that mediate pollinator behaviour. We investigated whether the large increase in emissions, mainly the monoterpene ß-myrcene (>90%), during daily thermogenic events of Macrozamia macleayi and lucida cycad cones are due solely to the influence of high cone temperatures or are, instead, a result of increased respiratory rates during thermogenesis. We concurrently measured temperature, oxygen consumption and ß-myrcene emission profiles during thermogenesis of pollen cones under typical environmental temperatures and during experimental manipulations of cone temperatures and aerobic conditions, all in the dark. The exponential rise in ß-myrcene emissions never occurred without a prior, large increase in respiration, whereas an increase in cone temperature alone did not increase emissions. When respiration during thermogenesis was interrupted by anoxic conditions, ß-myrcene emissions decreased. The increased emission rates are not a result of increased cone temperature per se (through increased enzyme activity or volatilization of stored volatiles) but are dependent on biosynthetic pathways associated with increased respiration during thermogenesis that provide the carbon, energy (ATP) and reducing compounds (NADPH) required for ß-myrcene production through the methylerythritol phosphate (MEP) pathway. These findings establish the significant contribution of respiration to volatile production during thermogenesis.

  7. Plant specific volatile organic compound emission factors from young and mature leaves of Mediterranean vegetation

    NASA Astrophysics Data System (ADS)

    Bracho-Nunez, Araceli; Welter, Saskia; Staudt, Michael; Kesselmeier, Jürgen

    2010-05-01

    Terrestrial vegetation is the most important source of atmospheric volatile organic compounds (VOC) with significant influence on the chemistry and physics of the atmosphere. VOCs influence the oxidative capacity of the atmosphere and contribute to the formation and growth of secondary organic aerosols affecting cloud development and precipitation. The aim of our study was to investigate potential quantitative and qualitative differences in VOC emission patterns of young and mature leaves for nine typical Mediterranean plant species. The Mediterranean area was chosen due to its special diversity in VOC emitting plant species. Foliar isoprenoid emissions as well as emissions of oxygenated VOC like methanol and acetone were measured under standard light and temperature conditions during spring and summer 2008 at the CEFE-CNRS institute in Montpellier, France. A proton transfer reaction mass spectrometer (PTR-MS) was used for online measurement of VOCs. While PTR-MS is an excellent technique for fast chemical measurements it lacks specificity and compounds with the same mass cannot be distinguished. For this reason, cartridge samples were collected and afterwards analyzed with GC-FID. In parallel offline VOC analyses were performed with gas chromatography (GC) coupled to a mass spectrometer and flame ionization detector, enabling assignment of the observed PTR-MS mass to charge ratios (m/z) to specific identification based on the GC-FID retention times. Thus, combining the PTR-MS and GC-FID analyses enabled accurate and online identification of the VOCs emitted. The results emphasise that VOC emission is a developmentally regulated process and quantitative and qualitative variability is plant species specific. Leaf ontogeny clearly influenced not only the standard emission rate but also the VOC composition, with methanol being the major compound that contributes to the total VOC emissions in young leaves and maintaining or decreasing its contribution with maturity.

  8. Emission of reactive terpene compounds from orange orchards and their removal by within-canopy processes

    NASA Astrophysics Data System (ADS)

    Ciccioli, Paolo; Brancaleoni, Enzo; Frattoni, Massimiliano; di Palo, Vincenzo; Valentini, Riccardo; Tirone, Giampiero; Seufert, Guenther; Bertin, Nadia; Hansen, Ute; Csiky, Olav; Lenz, Roman; Sharma, Meeta

    1999-04-01

    VOC emission from orange orchards was determined in the framework of two field campaigns aimed at assessing the contribution of vegetation emissions to tropospheric ozone formation in the Valencia Citrus belt. Branch emission from different varieties of Citrus sinensis and Citrus Clementi was dominated by β-caryophyllene during the summer period and by linalool during the blossoming season (April-May). Large emission of D-limonene from soil was also measured. Data collected with the enclosure technique were upscaled to determine canopy emission rates of terpene compounds. Values obtained were compared with fluxes measured by relaxed eddy accumulation. Substantial removal of β-caryophyllene and linalool was detected during transport from the canopy into the atmospheric boundary layer. While within-canopy removal of the sesquiterpene component was fully consistent with laboratory studies indicating the high reactivity of this compound with ozone, linalool losses were more difficult to explain. Although high canopy fluxes of acetone and acetaldehyde suggested linalool decomposition by gas-phase reactivity, removal by heterogeneous chemistry seems the more likely explanation for the observed losses.

  9. European Biogenic Volatile Organic Compound emissions estimate using MEGAN v2.10

    NASA Astrophysics Data System (ADS)

    Dawoud, M.; Pozzoli, L.; Unal, A.; Kindap, T.; Poupkou, A.; Katragou, E.; Melas, D.

    2013-12-01

    Biogenic emissions estimations are essential to obtain a comprehensive understanding of both anthropogenic and biogenic contributions of the emissions. In this paper we have calculated the Biogenic Volatile Organic Compound (BVOC) emissions from vegetation over Europe using the newly developed Model of Emissions of Gases and Aerosols from Nature version 2.10 (MEGAN2.10). We performed a simulation of the entire year 2008 for a domain covering all Europe at a resolution of 30 x 30 km. The meteorological fields needed to calculate the BVOC emissions (surface temperature and shortwave radiation) were provided by a WRFv3.3 simulation (driven by NCEP/FNL global reanalysis data at 1° x 1°) and interfaced to MEGAN with MCIPv3.6. We used the global dataset provided with the MEGAN2.10 model containing the Plant Functional Types (PFT, at 0.5° x 0.5°), Leaf Area Indices (LAI, at 30s resolution) and Emission Factors (EF, at 0.01° x 0.01°). The motivation behind this study is to quantify the biogenic emissions as calculated from the new version of MEGAN over Europe for the entire annual cycle, and in second step to quantify the impact of biogenic emissions on air quality, using the Community Multiscale Air Quality model (CMAQ). Isoprene emissions comprise about half of the total global biogenic volatile organic compound (BVOC) estimated using MEGAN2.10, while all Terpenes comprise about 18% of the estimated total global BVOC emissions. Our simulations showed that Isoprene emissions are ranging from 10.7 Gg/month in December to 6572.8 Gg/month over Europe in July, while Terpenes emissions range from 38 Gg/month in January and 1598.23 Gg/month in July. Around 15 Tg/year and 5 Tg/year are estimated as total annual emissions of Isoprene and Terpenes, respectively. In comparison with a previous study using the Natural Emission Model (NEMO), for the same period and the similar domain and resolution, for July we found 70% higher Isoprene emissions and 30% lower Terpenes emissions

  10. Extended Research on Detection of Deception Using Volatile Organic Compound (VOC) Emissions

    SciTech Connect

    Center for Human Reliability Studies

    2006-06-01

    A system that captures and analyzes volatile organic compound (VOC) emissions from skin surfaces may offer a viable alternative method to the polygraph instrument currently in use for detecting deception in U.S. government settings. Like the involuntary autonomic central nervous system response data gathered during polygraph testing, VOC emissions from the skin may provide data that can be used to detect stress caused by deception. Detecting VOCs, then, may present a noninvasive, non-intrusive method for observing, recording, and quantifying evidence of stress or emotional change.

  11. Contribution of flowering trees to urban atmospheric biogenic volatile organic compound emissions

    NASA Astrophysics Data System (ADS)

    Baghi, R.; Helmig, D.; Guenther, A.; Duhl, T.; Daly, R.

    2012-03-01

    Emissions of biogenic volatile organic compounds (BVOC) from urban trees during and after blooming were measured during spring and early summer 2009 in Boulder, Colorado. Air samples were collected onto solid adsorbent cartridges from branch enclosures on the tree species crabapple, horse chestnut, honey locust, and hawthorn. These species constitute ~65 % of the insect-pollinated fraction of the flowering tree canopy (excluding catkin-producing trees) from the street area managed by the City of Boulder. Samples were analyzed for C10-C15 BVOC by thermal desorption and gas chromatography coupled to a flame ionization detector and a mass spectrometer (GC/FID/MS). Identified emissions and emission rates from these four tree species during the flowering phase were found to vary over a wide range. Monoterpene emissions were identified for honey locust, horse chestnut and hawthorn. Sesquiterpene emissions were observed in horse chestnut and hawthorn samples. Crabapple flowers were found to emit significant amounts of benzyl alcohol and benzaldehyde. Floral BVOC emissions increased with temperature, generally exhibiting exponential temperature dependence. Changes in BVOC speciation during and after the flowering period were observed for every tree studied. Emission rates were significantly higher during the blooming compared to the vegetative state for crabapple and honey locust. Total normalized (30 °C) monoterpene emissions from honey locust were higher during flowering (5.26 μg Cg-1 h-1) than after flowering (1.23 μg Cg-1 h-1). The total normalized BVOC emission rate from crabapple (93 μg Cg-1 h-1) during the flowering period is of the same order as isoprene emissions from oak trees, which are among the highest BVOC emissions observed from plants to date. These findings illustrate that during the relatively brief springtime flowering period, floral emissions constitute by far the most significant contribution to the BVOC flux from these tree species, some of which

  12. Contribution of flowering trees to urban atmospheric biogenic volatile organic compound emissions

    NASA Astrophysics Data System (ADS)

    Baghi, R.; Helmig, D.; Guenther, A.; Duhl, T.; Daly, R.

    2012-04-01

    Emissions of biogenic volatile organic compounds (BVOC) from urban trees during and after blooming were measured during spring and early summer 2009 in Boulder, Colorado. Air samples were collected onto solid adsorbent cartridges from branch enclosures on the following trees: crabapple, horse chestnut, honey locust and hawthorn. These species constitute ~65% of the insect-pollinated fraction of the flowering tree canopy (excluding catkin-producing trees) from the total street area managed by the City of Boulder. Samples were subsequently analyzed for C10 - C15 BVOC by thermal desorption and gas chromatography coupled to a flame ionization detector and a mass spectrometer (GC/FID/MS). Identified emissions and emission rates from these four tree species during the flowering phase were found to vary over a wide range. Monoterpene emissions were identified for honey locust, horse chestnut and hawthorn. Sesquiterpene emissions were observed in horse chestnut and hawthorn samples. Crabapple flowers were found to emit significant amounts of benzyl alcohol and benzaldehyde. Floral BVOC emissions were found to increase with temperature, generally exhibiting exponential temperature dependence. Changes in BVOC speciation during and after the flowering period were observed for every tree studied. Emission rates were significantly higher during the blooming compared to the vegetative state for crabapple and honey locust. Total normalized (30oC) monoterpene emissions from honey locust were 4.3 fold higher during flowering (5.26 μgC g-1h-1) than after flowering (1.23 μgC g-1h-1). The total normalized BVOC emission rate from crabapple (93 μgC g-1h-1) during the flowering period is of the same order as isoprene emissions from oak trees, which are among the highest BVOC emissions observed to date. These findings illustrate that during the relatively brief springtime flowering period, floral emissions constitute by far the most significant contribution to the BVOC flux from these

  13. Patterns in volatile organic compound emissions along a savanna-rainforest gradient in central Africa

    NASA Astrophysics Data System (ADS)

    Klinger, L. F.; Greenburg, J.; Guenther, A.; Tyndall, G.; Zimmerman, P.; M'bangui, M.; Moutsamboté, J.-M.; Kenfack, D.

    1998-01-01

    In temperate regions the chemistry of the lower troposphere is known to be significantly affected by biogenic volatile organic compounds (VOCs) emitted by plants. The chemistry of the lower troposphere over the tropics, however, is poorly understood, in part because of the considerable uncertainties in VOC emissions from tropical ecosystems. Present global VOC models predict that base emissions of isoprene from tropical rainforests are considerably higher than from savannas. These global models of VOC emissions which rely mainly on species inventories are useful, but significant improvement might be made with more ecologically based models of VOC emissions by plants. Ecosystems along a successional transect from woodland savanna to primary rainforest in central Africa were characterized for species composition and vegetation abundance using ground surveys and remotely sensed data. A total of 336 species (mostly trees) at 13 sites were recorded, and 208 of these were measured for VOC emissions at near-optimal light and temperature conditions using a leaf cuvette and hand-held photoionization detector (PID). A subset of 59 species was also sampled using conventional VOC emission techniques in order to validate the PID technique. Results of ecological and VOC emission surveys indicate both phylogenetic and successional patterns along the savanna-rainforest transect. Genera and families of trees which tend to emit isoprene include Lophira, Irvingia, Albizia, Artocarpus, Ficus, Pterocarpus, Caesalpiniaceae, Arecaceae, and Moraceae. Other taxa tend to contain stored VOCs (Annonaceae and Asteraceae). Successional patterns suggest that isoprene emissions are highest in the relatively early successional Isoberlinia forest communities and progressively decrease in the later successional secondary and primary rainforest communities. Stored VOCs appear to increase along the savanna-rainforest succession, but these data are more tentative. These findings are consistent with

  14. Emissions of volatile organic compounds from hybrid poplar depend on CO2 concentration and genotype

    NASA Astrophysics Data System (ADS)

    Eller, A. S.; de Gouw, J. A.; Monson, R. K.

    2010-12-01

    Hybrid poplar is a fast-growing tree species that is likely to be an important source of biomass for the production of cellulose-based biofuels and may influence regional atmospheric chemistry through the emission of volatile organic compounds (VOCs). We used proton-transfer reaction mass spectrometry to measure VOC emissions from the leaves of four different hybrid poplar genotypes grown under ambient (400 ppm) and elevated (650 ppm) carbon dioxide concentration (CO2). The purpose of this experiment was to determine whether VOC emissions are different among genotypes and whether these emissions are likely to change as atmospheric CO2 rises. Methanol and isoprene made up over 90% of the VOC emissions and were strongly dependent on leaf age, with young leaves producing primarily methanol and switching to isoprene production as they matured. Monoterpene emissions were small, but tended to be higher in young leaves. Plants grown under elevated CO2 emitted smaller quantities of both methanol and isoprene, but the magnitude of the effect was dependent on genotype. Isoprene emission rates from mature leaves dropped from ~35 to ~28 nmol m-2 s-1 when plants were grown under elevated CO2. Emissions from individuals grown under ambient CO2 varied more based on genotype than those grown under elevated CO2, which means that we might expect smaller differences between genotypes in the future. Genotype and CO2 also affected how much carbon (C) individuals allocated to the production of VOCs. The emission rate of C from VOCs was 0.5 - 2% of the rate at which C was assimilated via net photosynthesis. The % C emitted was strongly related to genotype; clones from crosses between Populus deltoides and P. trichocarpa (T x D) allocated a greater % of their C to VOC emissions than clones from crosses of P. deltoids and P. nigra (D x N). Individuals from all four genotypes allocated a smaller % of their C to the emission of VOCs when they were grown under elevated CO2. These results

  15. Large drought-induced variations in oak leaf volatile organic compound emissions during PINOT NOIR 2012.

    PubMed

    Geron, Chris; Daly, Ryan; Harley, Peter; Rasmussen, Rei; Seco, Roger; Guenther, Alex; Karl, Thomas; Gu, Lianhong

    2016-03-01

    Leaf-level isoprene and monoterpene emissions were collected and analyzed from five of the most abundant oak (Quercus) species in Central Missouri's Ozarks Region in 2012 during PINOT NOIR (Particle Investigations at a Northern Ozarks Tower - NOx, Oxidants, Isoprene Research). June measurements, prior to the onset of severe drought, showed isoprene emission rates and leaf temperature responses similar to those previously reported in the literature and used in Biogenic Volatile Organic Compound (BVOC) emission models. During the peak of the drought in August, isoprene emission rates were substantially reduced, and response to temperature was dramatically altered, especially for the species in the red oak subgenus (Erythrobalanus). Quercus stellata (in the white oak subgenus Leucobalanus), on the other hand, increased its isoprene emission rate during August, and showed no decline at high temperatures during June or August, consistent with its high tolerance to drought and adaptation to xeric sites at the prairie-deciduous forest interface. Mid-late October measurements were conducted after soil moisture recharge, but were affected by senescence and cooler temperatures. Isoprene emission rates were considerably lower from all species compared to June and August data. The large differences between the oaks in response to drought emphasizes the need to consider BVOC emissions at the species level instead of just the whole canopy. Monoterpene emissions from Quercus rubra in limited data were highest among the oaks studied, while monoterpene emissions from the other oak species were 80-95% lower and less than assumed in current BVOC emission models. Major monoterpenes from Q. rubra (and in ambient air) were p-cymene, α-pinene, β-pinene, d-limonene, γ-terpinene, β-ocimene (predominantly1,3,7-trans-β-ocimene, but also 1,3,6-trans-β-ocimene), tricyclene, α-terpinene, sabinene, terpinolene, and myrcene. Results are discussed in the context of canopy flux studies

  16. Characteristics and reactivity of volatile organic compounds from non-coal emission sources in China

    NASA Astrophysics Data System (ADS)

    He, Qiusheng; Yan, Yulong; Li, Hongyan; Zhang, Yiqiang; Chen, Laiguo; Wang, Yuhang

    2015-08-01

    Volatile organic compounds (VOCs) were sampled from non-coal emission sources including fuel refueling, solvent use, industrial and commercial activities in China, and 62 target species were determined by gas chromatography-mass selective detector (GC-MSD). Based on the results, source profiles were developed and discussed from the aspects of composition characteristics, potential tracers, BTEX (benzene, toluene, ethylbenzene and xylene) diagnostic ratios and chemical reactivity. Compared with vehicle exhausts and liquid fuels, the major components in refueling emissions of liquefied petroleum gas (LPG), gasoline and diesel were alkenes and alkanes. Oppositely, aromatics were the most abundant group in emissions from auto-painting, book binding and plastic producing. Three groups contributed nearly equally in printing and commercial cooking emissions. Acetone in medical producing, chloroform and tetrachloroethylene in wet- and dry-cleaning, as well as TEX in plastic producing etc. were good tracers for the respective sources. BTEX ratios showed that some but not all VOCs sources could be distinguished by B/T, B/E and B/X ratios, while T/E, T/X and E/X ratios were not suitable as diagnostic indicators of different sources. The following reactivity analysis indicated that emissions from gasoline refueling, commercial cooking, auto painting and plastic producing had high atmospheric reactivity, and should be controlled emphatically to prevent ozone pollution, especially when there were large amounts of emissions for them.

  17. Emissions of volatile organic compounds from new carpets measured in a large-scale environmental chamber

    SciTech Connect

    Hodgson, A.T.; Wooley, J.D.; Daisey, J.M. )

    1993-03-01

    This study was undertaken to quantify the emissions of volatile organic compounds (VOCs) released by new carpets. Samples of four typical carpets, including two with styrene-butadiene rubber (SBR) latex adhesive and two with different backings, were collected from the finish lines at manufacturers' mills. Individual VOCs released from these samples were identified, and their concentrations, emission rates and mass emissions were measured under simulated indoor conditions in a 20 m[sup 3] environmental chamber over one week periods. Concentrations and emission rates of VOCs emitted by a new SBR carpet were also measured in a house. The carpets emitted a variety of VOCs. The two SBR carpets primarily emitted 4-phenylcyclohexene (4-PCH), the source of [open quotes]new carpet[close quotes] odor, and styrene. The concentrations and emission rates of 4-PCH were similar for the two carpets, while the styrene values varied significantly. The carpet with a polyvinyl chloride backing emitted formaldehyde, vinyl acetate, isooctane, 1,2-propanediol, and 2-ethyl-1-hexanol. Of these, vinyl acetate and propanediol had the highest concentrations and emission rates. The carpet with a polyurethane backing primarily emitted butylated hydroxytoluene. With the exception of formaldehyde, little is known about the health effects of these VOCs at low concentrations. 23 refs., 3 figs., 6 tabs.

  18. Emissions of volatile organic compounds from new carpets measured in a large-scale environmental chamber.

    PubMed

    Hodgson, A T; Wooley, J D; Daisey, J M

    1993-03-01

    This study was undertaken to quantify the emissions of volatile organic compounds (VOCs) released by new carpets. Samples of four typical carpets, including two with styrene-butadiene rubber (SBR) latex adhesive and two with different backings, were collected from the finish lines at manufacturers' mills. Individual VOCs released from these samples were identified, and their concentrations, emission rates and mass emissions were measured under simulated indoor conditions in a 20 m3 environmental chamber over one week periods. Concentrations and emission rates of VOCs emitted by a new SBR carpet were also measured in a house. The carpets emitted a variety of VOCs. The two SBR carpets primarily emitted 4-phenylcyclohexene (4-PCH), the source of "new carpet" odor, and styrene. The concentrations and emission rates of 4-PCH were similar for the two carpets, while the styrene values varied significantly. The carpet with a polyvinyl chloride backing emitted formaldehyde, vinyl acetate, isooctane, 1,2-propanediol, and 2-ethyl-1-hexanol. Of these, vinyl acetate and propanediol had the highest concentrations and emission rates. The carpet with a polyurethane backing primarily emitted butylated hydroxytoluene. With the exception of formaldehyde, little is known about the health effects of these VOCs at low concentrations.

  19. Anthropogenic emissions of highly reactive volatile organic compounds inferred from oversampling of OMI HCHO columns

    NASA Astrophysics Data System (ADS)

    Zhu, L.; Jacob, D. J.; Mickley, L. J.; Marais, E. A.; Cohan, D. S.; Yoshida, Y.; Duncan, B. N.; Gonzalez Abad, G.; Chance, K.

    2014-12-01

    Satellite observations of formaldehyde (HCHO) columns provide top-down constraints on emissions of highly reactive volatile organic compounds (HRVOCs). This approach has been used previously to constrain emissions of isoprene from vegetation, but application to US anthropogenic emissions has been stymied by lack of a discernable HCHO signal. Here we show that oversampling of HCHO data from the Ozone Monitoring Instrument (OMI) for 2005-2008 enables quantitative detection of urban and industrial plumes in eastern Texas including Houston, Port Arthur, and Dallas/Fort Worth. By spatially integrating the individual urban/industrial HCHO plumes observed by OMI we can constrain the corresponding HCHO-weighted HRVOC emissions. Application to the Houston plume indicates a HCHO source of 260±110 kmol h-1 and implies a factor of 5.5±2.4 underestimate of anthropogenic HRVOC emissions in the US Environmental Protection Agency inventory. This approach allows us to monitor trends in HRVOC emissions over the US, in particular from the urban areas and oil/gas industry.

  20. Emission characteristics of particulate matter and volatile organic compounds in cow dung combustion.

    PubMed

    Park, Duckshin; Barabad, Mona L; Lee, Gwangjae; Kwon, Soon-Bark; Cho, Youngmin; Lee, Duckhee; Cho, Kichul; Lee, Kiyoung

    2013-11-19

    Biomass fuel is used for cooking and heating, especially in developing countries. Combustion of biomass fuel can generate high levels of indoor air pollutants, including particulate matter (PM) and volatile organic compounds (VOCs). This study characterized PM and VOC emissions from cow dung combustion in a controlled experiment. Dung from grass-fed cows was dried and combusted using a dual-cone calorimeter. Heat fluxes of 10, 25, and 50 kW/m(2) were applied. The concentrations of PM and VOCs were determined using a dust spectrometer and gas chromatography/mass spectrometry, respectively. PM and VOC emission factors were much higher for the lower heat flux, implying a fire ignition stage. When the heat flux was 50 kW/m(2), the CO2 emission factor was highest and the PM and VOC emission factors were lowest. Particle concentrations were highest in the 0.23-0.3 μm size range at heat fluxes of 25 and 50 kW/m(2). Various toxic VOCs, including acetone, methyl ethyl ketone, benzene, and toluene, were detected at high concentrations. Although PM and VOC emission factors at 50 kW/m(2) were lower, they were high enough to cause extremely high indoor air pollution. The characteristics of PM and VOC emissions from cow dung combustion indicated potential health effects of indoor air pollution in developing countries.

  1. Anthropogenic Emissions of Highly Reactive Volatile Organic Compounds (HRVOCs) Inferred from Oversampling of OMI HCHO Columns

    NASA Technical Reports Server (NTRS)

    Zhu, Lei; Jacob, Daniel; Mickley, Loretta; Marais, Eloise; Zhang, Aoxing; Cohan, Daniel; Yoshida, Yasuko; Duncan, Bryan; Abad, Gonzalo Gonzalez; Chance, Kelly; DeSmedt, Isabelle

    2014-01-01

    Satellite observations of formaldehyde (HCHO) columns provide top-down constraints on emissions of highly reactive volatile organic compounds (HRVOCs). This approach has been used previously to constrain emissions of isoprene from vegetation, but application to US anthropogenic emissions has been stymied by lack of a discernable HCHO signal. Here we show that oversampling of HCHO data from the Ozone Monitoring Instrument (OMI) for 2005 - 2008 enables quantitative detection of urban and industrial plumes in eastern Texas including Houston, Port Arthur, and Dallas-Fort Worth. By spatially integrating the individual urban-industrial HCHO plumes observed by OMI we can constrain the corresponding HCHO-weighted HRVOC emissions. Application to the Houston plume indicates a HCHO source of 260 plus or minus 110 kmol h-1 and implies a factor of 5.5 plus or minus 2.4 underestimate of anthropogenic HRVOC emissions in the US Environmental Protection Agency inventory. With this approach we are able to monitor the trend in HRVOC emissions over the US, in particular from the oil-gas industry, over the past decade.

  2. Emission of oxygenated volatile organic compounds (OVOCs) during the aerobic decomposition of orange wastes.

    PubMed

    Wu, Ting; Wang, Xinming

    2015-07-01

    Oxygenated volatile organic compounds (OVOCs) emitted from orange wastes during aerobic decomposition were investigated in a laboratory-controlled incubator for a period of two months. Emission of total OVOCs (TOVOCs) from orange wastes reached 1714 mg/dry kg (330 mg/wet kg). Ethanol, methanol, ethyl acetate, methyl acetate, 2-butanone and acetaldehyde were the most abundant OVOC species with shares of 26.9%, 24.8%, 20.3%, 13.9%, 2.8% and 2.5%, respectively, in the TOVOCs released. The emission fluxes of the above top five OVOCs were quite trivial in the beginning but increased sharply to form one "peak emission window" with maximums at days 1-8 until leveling off after 10 days. This type of "peak emission window" was synchronized with the CO2 fluxes and incubation temperature of the orange wastes, indicating that released OVOCs were mainly derived from secondary metabolites of orange substrates through biotic processes rather than abiotic processes or primary volatilization of the inherent pool in oranges. Acetaldehyde instead had emission fluxes decreasing sharply from its initial maximum to nearly zero in about four days, suggesting that it was inherent rather than secondarily formed. For TOVOCs or all OVOC species except 2-butanone and acetone, over 80% of their emissions occurred during the first week, implying that organic wastes might give off a considerable amount of OVOCs during the early disposal period under aerobic conditions.

  3. Organic compounds in biomass smoke from residential wood combustion: Emissions characterization at a continental scale

    NASA Astrophysics Data System (ADS)

    Fine, Philip M.; Cass, Glen R.; Simoneit, Bernd R. T.

    2002-11-01

    Wood smoke in the atmosphere often accounts for 20-30% of the ambient fine-particle concentrations. In communities where wood is burned for home heating, wood smoke can at times contribute the majority of the atmospheric fine-particle burden. Chemical mass balance receptor models that use organic compounds as tracers can be used to determine the contributions of different emission sources, including wood smoke, to atmospheric fine-particle samples. In order for organic chemical tracer techniques to be applied to communities across the United States, differences in wood smoke composition that arise from differences in the type of wood burned in various regions must be understood. A continental-scale accounting of particulate organic compound emissions from residential wood combustion has been constructed which helps to quantify the regional differences in wood smoke composition that exist between different parts of the United States. Data from a series of source tests conducted on 22 North American wood species have been used to assemble a national inventory of emissions for more than 250 individual organic compounds that are released from wood combustion in fireplaces and wood stoves in the United States. The emission rates of important wood smoke markers, such as levoglucosan, certain substituted syringols and guaiacols, and phytosterols vary greatly with wood type and combustor type. These differences at the level of individual wood type and combustion conditions translate into regional differences in the aggregate composition of ambient wood smoke. By weighting the source test results in proportion to the availability of firewood from specific tree species and the quantities of wood burned in each locale, it is possible to investigate systematic differences that exist between wood smokes from different regions of North America. The relative abundance of 10 major wood smoke components averaged over the emissions inventory in different regions of the United States

  4. Effect of habitat and age on variations in volatile organic compound (VOC) emissions from Quercus ilex and Pinus pinea

    NASA Astrophysics Data System (ADS)

    Street, R. A.; Owen, S.; Duckham, S. C.; Boissard, C.; Hewitt, C. N.

    A dynamic branch enclosure was used to measure emission rates of volatile organic compounds (VOCs) under field conditions from two common native Mediterranean species, Quercus ilex and Pinus pinea. In addition to α-pinene, β-pinene, sabinene, limonene and cineole, a suite of lesser known compounds were tentatively identified including cis- and trans-ocimene, cis- and trans-linalool oxide and sabinaketone. Emissions of isoprene from Quercus ilex were insignificant in comparison to those of the monoterpenes and were not detected from Pinus pinea. Variability in emission rates between two habitats, the forest and the dunes, were assessed for Quercus ilex. Temperature sensitivities of emissions and total summed emission rates from Quercus ilex were clearly related to environmental conditions. Emission rates from Pinus pinea showed great variability, but differences between normalised mean emission rates from mature forest and young plantation trees may be significant. Existing emission rate models were found to inadequately describe the observed data.

  5. Emissions of oxygenated volatile organic compounds from open crop burning in Yangtze River Delta region, China

    NASA Astrophysics Data System (ADS)

    Tanimoto, H.; Kudo, S.; Pan, X.; Inomata, S.; Saito, S.; Kanaya, Y.; Wang, Z.

    2013-12-01

    Measurements of volatile organic compounds (VOCs) were made by gas chromatography/flame ionization detection/mass spectrometry (GC/FID/MS) and proton transfer reaction-mass spectrometry (PTR-MS) at Rudong, a rural area of Central East China in June 2010. During the campaign we identified several plumes originated from open biomass burning by the simultaneous enhancements of carbon monoxide and acetonitrile. Based on positive matrix factorization (PMF) analysis, the contribution of biomass burning was in the range from 60 to 80% for the plumes. We found that oxygenated VOCs were predominant for these events. The emission ratios of OVOCs to CO for open crop burnings derived in this work were found to be high. Combined with the updated CO emissions of 12.7 Tg per year from crop burning, we estimated OVOC emissions from crop burning can be about 1.2 Tg per year, accounting for substantial amount of VOCs emitted from crop burning.

  6. [Preliminary study concerning emissions of the volatile organic compounds from cooking oils].

    PubMed

    He, Wan-Qing; Tian, Gang; Nie, Lei; Qu, Song; Li, Jing; Wang, Min-Yan

    2012-09-01

    Cooking oil fume is one of the important sources of atmospheric volatile organic compounds (VOCs), which are the key precursors of ozone and secondary organic aerosols in air. In this study, the production of cooking oil fume was simulated by heating typical pure vegetable oils (peanut oil, sunflower oil, soybean oil, olive oil and blend oil) at different temperatures in beakers to investigate the VOCs emission characteristics. The emitted VOCs were sampled with a Tenax adsorption tube and analyzed using GC-MS after thermal desorption. The results showed that the emission of VOCs increased with the increase of the heating temperature for all the investigated cooking oils, and at a given temperature, the blend oil emitted the lowest amount of VOCs. The VOCs emission intensity at different heating temperatures fitted well with binomial equations and ranged from 1.6-11.1 mg x (kg x min)(-1).

  7. Behavior of VOCs and carbonyl compounds emission from different types of wallpapers in Korea.

    PubMed

    Lim, Jungyun; Kim, Suejin; Kim, Arong; Lee, Wooseok; Han, Jinseok; Cha, Jun-Seok

    2014-04-17

    Emissions of volatile organic compounds (VOCs) and carbonyls from three types of commercially available wallpapers (i.e., PVC-coated, paper-backed, natural material-coated) in Korea were evaluated using a 20 L small chamber. A total of 332 products were tested for emission factors, frequencies of occurrence and composition ratios. Toluene and formaldehyde concentrations were below Korean standard values for all products; however, the total VOC (TVOC) concentrations exceeded current standards (4.0 mg/m²·h) for 30 products. The TVOC emission factor for PVC-coated wallpapers, for which polymer materials are used in the manufacturing process, was seven and 16 times higher than those of paper-backed and natural material-coated wallpapers, respectively. The detection frequencies for toluene and formaldehyde were the highest (82.5%) and fourth highest (79.5%), respectively among the 50 target chemical species. The composition ratios for BTEX ranged from 0.3% to 5.1% and unidentified VOCs, which were not qualitatively analyzed using standard gas methods, ranged from 90.2% to 94.8%. Among six carbonyl compounds (acrolein was not detected in any type of wallpaper), acetone had the highest concentrations in PVC-coated (44.6%) and paper-backed (66.6%) wallpapers. Formaldehyde emissions were highest (64.6%) for natural material-coated wallpapers, a result of the formaldehyde-based resin used in the manufacturing process for these products.

  8. Behavior of VOCs and Carbonyl Compounds Emission from Different Types of Wallpapers in Korea

    PubMed Central

    Lim, Jungyun; Kim, Suejin; Kim, ARong; Lee, Wooseok; Han, Jinseok; Cha, Jun-Seok

    2014-01-01

    Emissions of volatile organic compounds (VOCs) and carbonyls from three types of commercially available wallpapers (i.e., PVC-coated, paper-backed, natural material-coated) in Korea were evaluated using a 20 L small chamber. A total of 332 products were tested for emission factors, frequencies of occurrence and composition ratios. Toluene and formaldehyde concentrations were below Korean standard values for all products; however, the total VOC (TVOC) concentrations exceeded current standards (4.0 mg/m2·h) for 30 products. The TVOC emission factor for PVC-coated wallpapers, for which polymer materials are used in the manufacturing process, was seven and 16 times higher than those of paper-backed and natural material-coated wallpapers, respectively. The detection frequencies for toluene and formaldehyde were the highest (82.5%) and fourth highest (79.5%), respectively among the 50 target chemical species. The composition ratios for BTEX ranged from 0.3% to 5.1% and unidentified VOCs, which were not qualitatively analyzed using standard gas methods, ranged from 90.2% to 94.8%. Among six carbonyl compounds (acrolein was not detected in any type of wallpaper), acetone had the highest concentrations in PVC-coated (44.6%) and paper-backed (66.6%) wallpapers. Formaldehyde emissions were highest (64.6%) for natural material-coated wallpapers, a result of the formaldehyde-based resin used in the manufacturing process for these products. PMID:24747540

  9. Development of a material with reproducible emission of selected volatile organic compounds - μ-Chamber study.

    PubMed

    Nohr, Michael; Horn, Wolfgang; Wiegner, Katharina; Richter, Matthias; Lorenz, Wilhelm

    2014-07-01

    Volatile organic compounds (VOCs) found indoors have the potential to affect human health. Typical sources include building materials, furnishings, cleaning agents, etc. To address this risk, chemical emission testing is used to assess the potential of different materials to pollute indoor air. One objective of the European Joint Research Project "MACPoll" (Metrology for Chemical Pollutants in Air) aims at developing and testing a reference material for the quality control of the emission testing procedure. Furthermore, it would enable comparison of measurement results between test laboratories. The heterogeneity of the majority of materials makes it difficult to find a suitable reference sample. In the present study, styrene, 2-ethyl-1-hexanol, N-methyl-α-pyrrolidone, lindane, n-hexadecane, 1,2-dimethyl- and 1,2-di-n-butyl-phthalate were added to 12 commercially available lacquers (6 alkyd and 6 acrylic polymer based lacquers) serving as carrier substrate. After homogenization, the mixtures were loaded into a Markes Micro-Chamber/Thermal Extractor (μ-CTE™) for curing and investigation of the emission behavior for each compound. For almost all of the investigated chemicals, the preferred glossy acrylic lacquer showed emissions that were reproducible with a variation of less than 20% RSD. Such lacquer systems have therefore been shown to be good candidates for use as reference materials in inter-laboratory studies.

  10. Variation in biogenic volatile organic compound emission pattern of Fagus sylvatica L. due to aphid infection

    NASA Astrophysics Data System (ADS)

    Joó, É.; Van Langenhove, H.; Šimpraga, M.; Steppe, K.; Amelynck, C.; Schoon, N.; Müller, J.-F.; Dewulf, J.

    2010-01-01

    Volatile organic compounds (VOCs) have been the focus of interest to understand atmospheric processes and their consequences in formation of ozone or aerosol particles; therefore, VOCs contribute to climate change. In this study, biogenic VOCs (BVOCs) emitted from Fagus sylvatica L. trees were measured in a dynamic enclosure system. In total 18 compounds were identified: 11 monoterpenes (MT), an oxygenated MT, a homoterpene (C 14H 18), 3 sesquiterpenes (SQT), isoprene and methyl salicylate. The frequency distribution of the compounds was tested to determine a relation with the presence of the aphid Phyllaphis fagi L. It was found that linalool, (E)-β-ocimene, α-farnesene and a homoterpene identified as (E)-4,8-dimethyl-1,3,7-nonatriene (DMNT), were present in significantly more samples when infection was present on the trees. The observed emission spectrum from F. sylvatica L. shifted from MT to linalool, α-farnesene, (E)-β-ocimene and DMNT due to the aphid infection. Sabinene was quantitatively the most prevalent compound in both, non-infected and infected samples. In the presence of aphids α-farnesene and linalool became the second and third most important BVOC emitted. According to our investigation, the emission fingerprint is expected to be more complex than commonly presumed.

  11. Impacts of simulated herbivory on volatile organic compound emission profiles from coniferous plants

    DOE PAGES

    Faiola, C. L.; Jobson, B. T.; VanReken, T. M.

    2015-01-28

    The largest global source of volatile organic compounds (VOCs) in the atmosphere is from biogenic emissions. Plant stressors associated with a changing environment can alter both the quantity and composition of the compounds that are emitted. This study investigated the effects of one global change stressor, increased herbivory, on plant emissions from five different coniferous species: bristlecone pine (Pinus aristata), blue spruce (Picea pungens), western redcedar (Thuja plicata), grand fir (Abies grandis), and Douglas-fir (Pseudotsuga menziesii). Herbivory was simulated in the laboratory via exogenous application of methyl jasmonate (MeJA), a herbivory proxy. Gas-phase species were measured continuously with a gasmore » chromatograph coupled to a mass spectrometer and flame ionization detector (GC–MS–FID). Stress responses varied between the different plant types and even between experiments using the same set of saplings. The compounds most frequently impacted by the stress treatment were alpha-pinene, beta-pinene, 1,8-cineol, beta-myrcene, terpinolene, limonene, and the cymene isomers. Individual compounds within a single experiment often exhibited a different response to the treatment from one another.« less

  12. Impacts of simulated herbivory on volatile organic compound emission profiles from coniferous plants

    NASA Astrophysics Data System (ADS)

    Faiola, C. L.; Jobson, B. T.; VanReken, T. M.

    2015-01-01

    The largest global source of volatile organic compounds (VOCs) in the atmosphere is from biogenic emissions. Plant stressors associated with a changing environment can alter both the quantity and composition of the compounds that are emitted. This study investigated the effects of one global change stressor, increased herbivory, on plant emissions from five different coniferous species: bristlecone pine (Pinus aristata), blue spruce (Picea pungens), western redcedar (Thuja plicata), grand fir (Abies grandis), and Douglas-fir (Pseudotsuga menziesii). Herbivory was simulated in the laboratory via exogenous application of methyl jasmonate (MeJA), a herbivory proxy. Gas-phase species were measured continuously with a gas chromatograph coupled to a mass spectrometer and flame ionization detector (GC-MS-FID). Stress responses varied between the different plant types and even between experiments using the same set of saplings. The compounds most frequently impacted by the stress treatment were alpha-pinene, beta-pinene, 1,8-cineol, beta-myrcene, terpinolene, limonene, and the cymene isomers. Individual compounds within a single experiment often exhibited a different response to the treatment from one another.

  13. Emission rates of selected volatile organic compounds from skin of healthy volunteers.

    PubMed

    Mochalski, Paweł; King, Julian; Unterkofler, Karl; Hinterhuber, Hartmann; Amann, Anton

    2014-05-15

    Gas chromatography with mass spectrometric detection (GC-MS) coupled with solid phase micro-extraction as pre-concentration method (SPME) was applied to identify and quantify volatile organic compounds (VOCs) emitted by human skin. A total of 64 C4-C10 compounds were quantified in skin emanation of 31 healthy volunteers. Amongst them aldehydes and hydrocarbons were the predominant chemical families with eighteen and seventeen species, respectively. Apart from these, there were eight ketones, six heterocyclic compounds, six terpenes, four esters, two alcohols, two volatile sulphur compounds, and one nitrile. The observed median emission rates ranged from 0.55 to 4,790 fmol cm(-2)min(-1). Within this set of analytes three volatiles; acetone, 6-methyl-5-hepten-2-one, and acetaldehyde exhibited especially high emission rates exceeding 100 fmol cm(-2)min(-1). Thirty-three volatiles were highly present in skin emanation with incidence rates over 80%. These species can be considered as potential markers of human presence, which could be used for early location of entrapped victims during Urban Search and Rescue Operations (USaR).

  14. Emission of volatile sulfur compounds during composting of municipal solid waste (MSW)

    SciTech Connect

    Zhang, Hongyu; Schuchardt, Frank; Li, Guoxue; Yang, Jinbing; Yang, Qingyuan

    2013-04-15

    Highlights: ► We compare the volatile sulfur compounds (VSCs) emissions during three types of municipal solid wastes (MSWs) composting. ► The VSCs released from the kitchen waste composting was significantly higher than that from 15–80 mm fraction of MSW. ► Among the five VSCs, H{sub 2}S was the most abundant compound with 39.0–43.0% of total VSCs released. ► Addition of 20% cornstalks could significantly reduce the VSCs emissions during kitchen waste composting. - Abstract: Volatile sulfur compounds (VSCs) are the main source for malodor from composting plants. In this study, the VSCs generated from composting of 15–80 mm municipal solid waste (T0), kitchen waste (T1) and kitchen waste mixed dry cornstalks (T2) were measured in 60 L reactors with forced aeration for a period of 30 days. The VSCs detected in all treatments were hydrogen sulfide (H{sub 2}S), methyl mercaptan (MM), dimethyl sulfide (DMS), carbon bisulfide (CS{sub 2}) and dimethyl disulfide (DMDS). Over 90% of the VSCs emissions occurred during the first 15 days, and reached their peak values at days 4–7. The emission profiles of five VSCs species were significantly correlated with internal materials temperature and outlet O{sub 2} concentration (p < 0.05). Total emissions of the VSCs were 216.1, 379.3 and 126.0 mg kg{sup −1} (dry matter) for T0, T1 and T2, respectively. Among the five VSCs, H{sub 2}S was the most abundant compound with 39.0–43.0% of total VSCs released. Composting of kitchen waste from separate collection posed a negative influence on the VSC and leachate production because of its high moisture content. An addition of dry cornstalks at a mixing ratio of 4:1 (wet weight) could significantly reduce the VSCs emissions and avoid leachate. Compared to pure kitchen waste, VSCs were reduced 66.8%.

  15. Investigating Sources and Emissions of Volatile Organic Compounds in California's San Joaquin Valley

    NASA Astrophysics Data System (ADS)

    Gentner, D. R.; Harley, R. A.; Weber, R.; Karlik, J. F.; Goldstein, A. H.

    2011-12-01

    Emissions of Volatile Organic Compounds (VOCs) are regulated both as primary air pollutants and as precursors to the formation of secondary organic aerosol and tropospheric ozone. The San Joaquin Valley, a non-attainment area for ozone and PM2.5, contains a variety of point, area, and mobile VOC sources that contribute to both primary and secondary pollution. Using ambient measurements of over 100 different VOCs and Intermediate Volatility Organic Compounds (IVOCs) made at multiple field sites, we assess the magnitude and importance of various VOC sources in the San Joaquin Valley. Hourly measurements were made during the spring and summer of 2010 via in-situ gas chromatography in Bakersfield, CA as part of the CalNex experiment and also at a rural site located 100 km north of Bakersfield. Additionally, in-situ measurements of fresh motor vehicle exhaust were made in Oakland's Caldecott tunnel during the summer of 2010. Measurements include a broad array of anthropogenic and biogenic VOCs ranging in size from 1 to 17 carbon atoms, including many compounds with functional groups or substituents (e.g. aldehydes, ketones, alcohols, halogens, sulfur, & nitrogen). Using statistical methods of source apportionment, covariance, source receptor modeling, and air parcel back trajectories, we assess the impact of various sources on observed VOC concentrations at our field sites in the San Joaquin Valley. Prevalent sources include gasoline and diesel-vehicle exhaust, petroleum extraction/refining, biogenic emissions from agricultural crops and natural vegetation, and emissions from dairy operations and animal husbandry. We use measurements of fresh motor vehicle emissions from the Caldecott tunnel to constrain apportionment of gasoline and diesel-related VOCs and IVOCs in the San Joaquin Valley. Initial results from Bakersfield show substantial influence from local anthropogenic VOC sources, but there is evidence for transport of emissions from both anthropogenic and biogenic

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

    NASA Astrophysics Data System (ADS)

    Swarthout, Robert F.

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

  17. Emissions and Chemistry of Volatile Organic Compounds in Early Spring of Western U.S.: Interactions between Oil/Gas Emissions and Biogenic Emissions

    NASA Astrophysics Data System (ADS)

    Yuan, B.; Koss, A.; Warneke, C.; Gilman, J.; Lerner, B. M.; Peischl, J.; Ryerson, T. B.; Sjostedt, S. J.; Thompson, C. R.; Wild, R. J.; Brown, S. S.; Neuman, J. A.; Eilerman, S. J.; Wolfe, G. M.; St Clair, J. M.; Hanisco, T. F.; Thayer, M. P.; Keutsch, F. N.; De Gouw, J. A.

    2015-12-01

    A series of research flights with the NOAA WP-3D aircraft were conducted during the SONGNEX campaign (www.esrl.noaa.gov/csd/projects/songnex) to characterize emissions of trace gases from oil and gas basins in the western United States and their chemical transformations. Volatile organic compounds (VOCs) were measured by a newly developed chemical ionization mass spectrometer that uses H3O+ for ionization and a high-resolution time-of-flight mass spectrometer for detection (H3O+ CIMS). Results from the measurements will be presented at the meeting. Emission fluxes of VOCs can be determined both by the mass balance and eddy covariance methods. To investigate the potential for eddy covariance flux measurements, we focus on two flights conducted over the Haynesville shale basin on April 4 and April 25, 2015, respectively. Much higher concentrations of biogenic VOCs (isoprene, monoterpenes and methanol) were measured during the flight on April 25, 2015, which provides an opportunity to evaluate our instrument for the eddy covariance technique. Emissions and deposition of various hydrocarbons and oxygenated VOCs are determined and flux divergence derived from flux estimates at different altitudes is used to explore formation and loss processes of organic species in the boundary layer. Based on results from the eddy covariance technique, we will discuss some implications on distribution of emission strength in an oil/gas basin, i.e. what is the relative importance of high versus low emitters to the total emissions. We will also investigate the roles of biogenic emissions in the chemical evolution of oil and gas emissions by comparing the two flights.

  18. Trends, temporal and spatial characteristics, and uncertainties in biomass burning emissions in the Pearl River Delta, China

    NASA Astrophysics Data System (ADS)

    He, Min; Zheng, Junyu; Yin, Shasha; Zhang, Yingyi

    2011-08-01

    Multi-year inventories of biomass burning emissions were established in the Pearl River Delta (PRD) region for the period 2003-2007 based on the collected activity data and emission factors. The results indicated that emissions of sulfur dioxide (SO 2), nitrogen oxide (NO x), ammonia (NH 3), methane (CH 4), organic carbon (OC), non-methane volatile organic compounds (NMVOC), carbon monoxide (CO), and fine particulate matter (PM 2.5) presented clear declining trends. Domestic biofuel burning was the major contributor, accounting for more than 60% of the total emissions. The preliminary temporal profiles were established with MODIS fire count information, showing that higher emissions were observed in winter (from November to March) than other seasons. The emissions were spatially allocated into grid cells with a resolution of 3 km × 3 km, using GIS-based land use data as spatial surrogates. Large amount of emissions were observed mostly in the less developed areas in the PRD region. The uncertainties in biomass burning emission estimates were quantified using Monte Carlo simulation; the results showed that there were higher uncertainties in organic carbon (OC) and elemental carbon (EC) emission estimates, ranging from -71% to 133% and -70% to 128%, and relatively lower uncertainties in SO 2, NO x and CO emission estimates. The key uncertainty sources of the developed inventory included emission factors and parameters used for estimating biomass burning amounts.

  19. Ozone formation potentials of organic compounds from different emission sources in the South Coast Air Basin of California

    NASA Astrophysics Data System (ADS)

    Chen, Jianjun; Luo, Dongmin

    2012-08-01

    Different organic compounds exhibit different propensities for ozone formation. Two approaches were used to study the ozone formation potentials or source reactivities of different anthropogenic organic compounds emission categories in California's South Coast Air Basin (SoCAB). The first approach was based on the combination of total organic gases (TOG) emission speciation profiles and the maximum incremental reactivity (MIR) scale of organic species. The second approach quantified ozone impacts from different emission sources by performing 3-dimensional air quality model sensitivity analysis involving increased TOG emissions from particular sources. The source reactivities derived from these two approaches agree reasonably well for 58 anthropogenic organic compounds emission categories in the SoCAB. Both approaches identify TOG emissions from mobile sources as having the highest reactivity. Source reactivities from both approaches were also combined with TOG emissions from each source category to produce a 2005 reactivity-based anthropogenic TOG emission inventory for the SoCAB. The top five reactivity-based anthropogenic TOG emission sources in the SoCAB during 2005 were: light-duty passenger cars, off-road equipment, consumer products, light-duty trucks category 2 (i.e., 3751-5750 lb), and recreational boats. This is in contrast to the mass-based TOG emission inventory, which indicates that livestock waste and composting emission categories were two of the five largest mass-based anthropogenic TOG emission sources. The reactivity-based TOG emission inventory is an important addition to the mass-based TOG emission inventory because it represents the ozone formation potentials from emission sources and can be used to assist in determining targeted sources for developing organic compounds reduction policies.

  20. Measurements of volatile organic compound (VOC) emissions from wood stains using an electronic balance

    SciTech Connect

    Zhang, J.S.; Nong, G.; Shaw, C.Y.; Wang, J.

    1999-07-01

    An emissions test method using an electronic balance is introduced for measuring the TVOC emission rates of oil-based wood stains, with a detailed procedure for preparing test specimens. The emission characteristics of volatile organic compounds (VOC) from an artificial wood stain and an oil-based commercial wood stain were determined. Results showed that VOC emissions from both stains included a surface evaporation and an internal diffusion sub-process. With regard to time, the entire emission period could be divided into three periods: (1) an initial evaporation-controlled period that was characterized by a high and fast decaying emission rate, (2) a transition period (following the initial period) in which the emissions transited from an evaporation-controlled to an internal diffusion-controlled process, and (3) an internal diffusion-controlled period that was characterized by a low and slowly decaying emission rate. For the commercial wood stain tested, the length of the initial period was approximately three hours, and about 46% of the emittable VOC mass was emitted during this short period. The transition period was between 3 and 6.5 hours from the start of testing and only accounted for about 4% of VOC mass emitted. The rest (about 50%) of the VOC mass was emitted in the diffusion-controlled period over a long period of time. Comparison between the commercial wood stain and an artificial wood stain suggested that the pigments/solids in the wood stain had significant effect on the time scales and amount of mass emitted during each emission period. The presence of additional VOCs in the commercial wood stain might have also affected the emission profiles. These results are useful for developing better models for predicting the emission rates. The electronic balance method was also compared with those determined from the TVOC concentrations measured at the chamber exhaust (referred to as chamber method). Results show that the two methods agreed well with each

  1. Semivolatile and volatile organic compound emissions from wood-fired hydronic heaters.

    PubMed

    Aurell, Johanna; Gullett, Brian K; Tabor, Dennis; Touati, Abderrahmane; Oudejans, Lukas

    2012-07-17

    Emissions including polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs), polyaromatic hydrocarbons (PAHs), and volatile organic compounds (VOCs), were sampled from different wood-fired hydronic heater (HH) technologies. Four commercially available HH technologies were studied: a single-stage conventional combustor with natural updraft, a three-stage downdraft combustion system, a bottom-fed pellet burner, and a two-stage heater with both a combustion and gasification chamber. The fuel consisted of three wood types (red oak, white pine, and white ash), one hardwood pellet brand, and one fuel mixture containing 95% red oak and 5% residential refuse by weight. The various HHs and fuel combinations were tested in a realistic homeowner fuel-charging scenario. Differences in emission levels were found between HH technologies and fuel types. PCDD/PCDF emissions ranged from 0.004 to 0.098 ng toxic equivalency/MJ(input) and PAHs from 0.49 to 54 mg/MJ(input). The former was increased by the presence of 5% by weight refuse. The white pine fuel had the highest PAH emission factor, while the bottom fed pellet burner had the lowest. The major VOCs emitted were benzene, acetylene, and propylene. The highest emissions of PAHs, VOCs, and PCDDs/PCDFs were observed with the conventional unit, likely due to the rapid changes in combustion conditions effected by the damper opening and closing.

  2. The Amazonian Floodplains, an ecotype with challenging questions on volatile organic compound (VOC) emissions

    NASA Astrophysics Data System (ADS)

    Kesselmeier, J.

    2012-12-01

    Volatile organic compound (VOC) emissions are affected by a variety of biotic and abiotic factors such as light intensity, temperature, CO2 and drought. Another factor usually overlooked but very important for the tropical rainforest in Amazonia is regular flooding. According to recent estimates, the total Amazonian floodplain area easily ranges up to 700,000 km^2, including whitewater river floodplains (várzea) blackwater regions (igapó) and further clearwater regions. Regarding the total Amazonian wetlands the area sums up to more than 2.000.000 km^2, i.e. 30% of Amazonia. To survive the flooding periods causing anoxic conditions for the root system of up to several months, vegetation has developed several morphological, anatomical and physiological strategies. One is to switch over the root metabolism to fermentation, thus producing ethanol as one of the main products. Ethanol is a toxic metabolite which is transported into the leaves by the transpiration stream. From there it can either be directly emitted into the atmosphere, or can be re-metabolized to acetaldehyde and/or acetate. All of these compounds are volatile enough to be partly released into the atmosphere. We observed emissions of ethanol, acetaldehyde and acetic acid under root anoxia. Furthermore, plant stress induced by flooding also affected leaf primary physiological processes as well as other VOC emissions such as the release of isoprenoids and other volatiles. For example, Hevea spruceana could be identified as a monoterpene emitting tree species behaving differently upon anoxia depending on the origin, with increasing emissions of the species from igapó and decreasing with the corresponding species from várzea. Contrasting such short term inundations, studies of VOC emissions under long term conditions (2-3 months) did not confirm the ethanol/acetaldehyde emissions, whereas emissions of other VOC species decreased considerably. These results demonstrate that the transfer of our knowledge

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

    NASA Astrophysics Data System (ADS)

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

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

  4. A process-based emission model of volatile organic compounds from silage sources on farms

    NASA Astrophysics Data System (ADS)

    Bonifacio, H. F.; Rotz, C. A.; Hafner, S. D.; Montes, F.; Cohen, M.; Mitloehner, F. M.

    2017-03-01

    Silage on dairy farms can emit large amounts of volatile organic compounds (VOCs), a precursor in the formation of tropospheric ozone. Because of the challenges associated with direct measurements, process-based modeling is another approach for estimating emissions of air pollutants from sources such as those from dairy farms. A process-based model for predicting VOC emissions from silage was developed and incorporated into the Integrated Farm System Model (IFSM, v. 4.3), a whole-farm simulation of crop, dairy, and beef production systems. The performance of the IFSM silage VOC emission model was evaluated using ethanol and methanol emissions measured from conventional silage piles (CSP), silage bags (SB), total mixed rations (TMR), and loose corn silage (LCS) at a commercial dairy farm in central California. With transport coefficients for ethanol refined using experimental data from our previous studies, the model performed well in simulating ethanol emission from CSP, TMR, and LCS; its lower performance for SB could be attributed to possible changes in face conditions of SB after silage removal that are not represented in the current model. For methanol emission, lack of experimental data for refinement likely caused the underprediction for CSP and SB whereas the overprediction observed for TMR can be explained as uncertainty in measurements. Despite these limitations, the model is a valuable tool for comparing silage management options and evaluating their relative effects on the overall performance, economics, and environmental impacts of farm production. As a component of IFSM, the silage VOC emission model was used to simulate a representative dairy farm in central California. The simulation showed most silage VOC emissions were from feed lying in feed lanes and not from the exposed face of silage storages. This suggests that mitigation efforts, particularly in areas prone to ozone non-attainment status, should focus on reducing emissions during feeding. For

  5. Duration of emission of volatile organic compounds from mechanically damaged plant leaves.

    PubMed

    Smith, Lincoln; Beck, John J

    2015-09-01

    Classical biological control of invasive alien weeds depends on the use of arthropod herbivores that are sufficiently host specific to avoid risk of injuring nontarget plants. Host plant specificity is usually evaluated by using a combination of behavioral and developmental experiments under choice, no-choice and field conditions. Secondary plant compounds are likely to have an important influence on host plant specificity. However, relatively little is known about the volatile organic compounds (VOCs) that are emitted by target and nontarget plants, and how environmental conditions may affect their emission. Previous studies have shown that mechanical damage of leaves increases the composition and content of VOCs emitted. In this study we measured the VOC emissions of five species of plants in the subtribe Centaureinae (Asteraceae)--Carthamus tinctorius, Centaurea cineraria, Centaurea melitensis, Centaurea rothrockii, and Centaurea solstitialis--that have previously been used in host specificity experiments for a prospective biological control agent of yellow starthistle (C. solstitialis). Leaves of each plant were punctured with a needle and the VOCs were collected by solid-phase microextraction (SPME) periodically over 48 h and analyzed by GC-MS. A total of 49 compounds were detected. Damage caused an immediate increase of 200-600% in the composition of VOCs emitted from each plant species, and the amounts generally remained high for at least 48 h. The results indicate that a very unspecific mechanical damage can cause a prolonged change in the VOC profile of plants.

  6. L α X-Ray Emission Spectra of Copper Compounds and Alloys

    NASA Astrophysics Data System (ADS)

    Sugiura, Chikara

    1994-05-01

    With a two-crystal vacuum spectrometer equipped with beryl crystals,the Cu Lα emission spectra in fluorescence have been measuredfor selected copper compounds Cu2O, CuO, CuCl, CuBr, CuI,CuF2, CuCl2, CuBr2, CuF2·2H2O,CuCl2·2H2O and Cu3P, and alloysα-Cu+35%Zn and Cu+2%Be. The measured spectra aregrouped into three classes. The first class comprises the spectraof alloys, which consist of a single broad band similar to thatof Cu metal. The second class includes the spectra of monovalentcopper compounds, which are composed of a prominent peak and itshigh- and low-energy structures. To the third class belong thespectra of divalent copper compounds, which consist of a strongpeak accompanied with a characteristic dip and hump on thehigh-energy side. The Cu Lα emission bands of Cu2O,CuCl and CuBr are compared with available XPS spectra andtheoretical Cu-3d-DOS.

  7. Characterizing reduced sulfur compounds emissions from a swine concentrated animal feeding operation

    NASA Astrophysics Data System (ADS)

    Rumsey, Ian C.; Aneja, Viney P.; Lonneman, William A.

    2014-09-01

    Reduced sulfur compounds (RSCs) emissions from concentrated animal feeding operations (CAFOs) have become a potential environmental and human health concern, as a result of changes in livestock production methods. RSC emissions were determined from a swine CAFO in North Carolina. RSC measurements were made over a period of ≈1 week from both the barn and lagoon during each of the four seasonal periods from June 2007 to April 2008. During sampling, meteorological and other environmental parameters were measured continuously. Seasonal hydrogen sulfide (H2S) barn concentrations ranged from 72 to 631 ppb. Seasonal dimethyl sulfide (DMS; CH3SCH3) and dimethyl disulfide (DMDS; CH3S2CH3) concentrations were 2-3 orders of magnitude lower, ranging from 0.18 to 0.89 ppb and 0.47 to 1.02 ppb, respectively. The overall average barn emission rate was 3.3 g day-1 AU-1 (AU (animal unit) = 500 kg of live animal weight) for H2S, which was approximately two orders of magnitude higher than the DMS and DMDS overall average emissions rates, determined as 0.017 g day-1 AU-1 and 0.036 g day-1 AU-1, respectively. The overall average lagoon flux was 1.33 μg m-2 min-1 for H2S, which was approximately an order of magnitude higher than the overall average DMS (0.12 μg m-2 min-1) and DMDS (0.09 μg m-2 min-1) lagoon fluxes. The overall average lagoon emission for H2S (0.038 g day-1 AU-1) was also approximately an order of magnitude higher than the overall average DMS (0.0034 g day-1 AU-1) and DMDS (0.0028 g day-1 AU-1) emissions. H2S, DMS and DMDS have offensive odors and low odor thresholds. Over all four sampling seasons, 77% of 15 min averaged H2S barn concentrations were an order of magnitude above the average odor threshold. During these sampling periods, however, DMS and DMDS concentrations did not exceed their odor thresholds. The overall average barn and lagoon emissions from this study were used to help estimate barn, lagoon and total (barn + lagoon) RSC emissions from swine CAFOs

  8. Estimating European volatile organic compound emissions using satellite observations of formaldehyde from the Ozone Monitoring Instrument

    NASA Astrophysics Data System (ADS)

    Curci, G.; Palmer, P. I.; Kurosu, T. P.; Chance, K.; Visconti, G.

    2010-12-01

    Emission of non-methane Volatile Organic Compounds (VOCs) to the atmosphere stems from biogenic and human activities, and their estimation is difficult because of the many and not fully understood processes involved. In order to narrow down the uncertainty related to VOC emissions, which negatively reflects on our ability to simulate the atmospheric composition, we exploit satellite observations of formaldehyde (HCHO), an ubiquitous oxidation product of most VOCs, focusing on Europe. HCHO column observations from the Ozone Monitoring Instrument (OMI) reveal a marked seasonal cycle with a summer maximum and winter minimum. In summer, the oxidation of methane and other long-lived VOCs supply a slowly varying background HCHO column, while HCHO variability is dominated by most reactive VOC, primarily biogenic isoprene followed in importance by biogenic terpenes and anthropogenic VOCs. The chemistry-transport model CHIMERE qualitatively reproduces the temporal and spatial features of the observed HCHO column, but display regional biases which are attributed mainly to incorrect biogenic VOC emissions, calculated with the Model of Emissions of Gases and Aerosol from Nature (MEGAN) algorithm. These "bottom-up" or a-priori emissions are corrected through a Bayesian inversion of the OMI HCHO observations. Resulting "top-down" or a-posteriori isoprene emissions are lower than "bottom-up" by 40% over the Balkans and by 20% over Southern Germany, and higher by 20% over Iberian Peninsula, Greece and Italy. We conclude that OMI satellite observations of HCHO can provide a quantitative "top-down" constraint on the European "bottom-up" VOC inventories.

  9. Estimating European volatile organic compound emissions using satellite observations of formaldehyde from the Ozone Monitoring Instrument

    NASA Astrophysics Data System (ADS)

    Curci, G.; Palmer, P. I.; Kurosu, T. P.; Chance, K.; Visconti, G.

    2010-08-01

    Emission of non-methane Volatile Organic Compounds (VOCs) to the atmosphere stems from biogenic and human activities, and their estimation is difficult because of the many and not fully understood processes involved. In order to narrow down the uncertainty related to VOC emissions, which negatively reflects on our ability to simulate the atmospheric composition, we exploit satellite observations of formaldehyde (HCHO), an ubiquitous oxidation product of most VOCs, focusing on Europe. HCHO column observations from the Ozone Monitoring Instrument (OMI) reveal a marked seasonal cycle with a summer maximum and winter minimum. In summer, the oxidation of methane and other long-lived VOCs supply a slowly varying background HCHO column, while HCHO variability is dominated by most reactive VOC, primarily biogenic isoprene followed in importance by biogenic terpenes and anthropogenic VOCs. The chemistry-transport model CHIMERE qualitatively reproduces the temporal and spatial features of the observed HCHO column, but display regional biases which are attributed mainly to incorrect biogenic VOC emissions, calculated with the Model of Emissions of Gases and Aerosol from Nature (MEGAN) algorithm. These "bottom-up" or a-priori emissions are corrected through a Bayesian inversion of the OMI HCHO observations. Resulting "top-down" or a-posteriori isoprene emissions are lower than "bottom-up" by 40% over the Balkans and by 20% over Southern Germany, and higher by 20% over Iberian Peninsula, Greece and Italy. The inversion is shown to be robust against assumptions on the a-priori and the inversion parameters. We conclude that OMI satellite observations of HCHO can provide a quantitative "top-down" constraint on the European "bottom-up" VOC inventories.

  10. Gas phase carbonyl compounds in ship emissions: Differences between diesel fuel and heavy fuel oil operation

    NASA Astrophysics Data System (ADS)

    Reda, Ahmed A.; Schnelle-Kreis, J.; Orasche, J.; Abbaszade, G.; Lintelmann, J.; Arteaga-Salas, J. M.; Stengel, B.; Rabe, R.; Harndorf, H.; Sippula, O.; Streibel, T.; Zimmermann, R.

    2014-09-01

    Gas phase emission samples of carbonyl compounds (CCs) were collected from a research ship diesel engine at Rostock University, Germany. The ship engine was operated using two different types of fuels, heavy fuel oil (HFO) and diesel fuel (DF). Sampling of CCs was performed from diluted exhaust using cartridges and impingers. Both sampling methods involved the derivatization of CCs with 2,4-Dinitrophenylhydrazine (DNPH). The CCs-hydrazone derivatives were analyzed by two analytical techniques: High Performance Liquid Chromatography-Diode Array Detector (HPLC-DAD) and Gas Chromatography-Selective Ion Monitoring-Mass Spectrometry (GC-SIM-MS). Analysis of DNPH cartridges by GC-SIM-MS method has resulted in the identification of 19 CCs in both fuel operations. These CCs include ten aliphatic aldehydes (formaldehyde, acetaldehyde, propanal, isobutanal, butanal, isopentanal, pentanal, hexanal, octanal, nonanal), three unsaturated aldehydes (acrolein, methacrolein, crotonaldehyde), three aromatic aldehyde (benzaldehyde, p-tolualdehyde, m,o-molualdehyde), two ketones (acetone, butanone) and one heterocyclic aldehyde (furfural). In general, all CCs under investigation were detected with higher emission factors in HFO than DF. The total carbonyl emission factor was determined and found to be 6050 and 2300 μg MJ-1 for the operation with HFO and DF respectively. Formaldehyde and acetaldehyde were found to be the dominant carbonyls in the gas phase of ship engine emission. Formaldehyde emissions factor varied from 3500 μg MJ-1 in HFO operation to 1540 μg MJ-1 in DF operation, which is 4-30 times higher than those of other carbonyls. Emission profile contribution of CCs showed also a different pattern between HFO and DF operation. The contribution of formaldehyde was found to be 58% of the emission profile of HFO and about 67% of the emission profile of DF. Acetaldehyde showed opposite behavior with higher contribution of 16% in HFO compared to 11% for DF. Heavier carbonyls

  11. Characteristics of volatile organic compounds emission profiles from hot road bitumens.

    PubMed

    Boczkaj, Grzegorz; Przyjazny, Andrzej; Kamiński, Marian

    2014-07-01

    A procedure for the investigation and comparison of volatile organic compounds (VOCs) emission profiles to the atmosphere from road bitumens with various degrees of oxidation is proposed. The procedure makes use of headspace analysis and gas chromatography with universal as well as selective detection, including gas chromatography-mass spectrometry (GC-MS). The studies revealed that so-called vacuum residue, which is the main component of the charge, contains variable VOC concentrations, from trace to relatively high ones, depending on the extent of thermal cracking in the boiler of the vacuum distillation column. The VOC content in the oxidation product, so-called oxidized paving bitumen, is similarly varied. There are major differences in VOC emission profiles between vacuum residue and oxidized bitumens undergoing thermal cracking. The VOC content in oxidized bitumens, which did not undergo thermal cracking, increases with the degree of oxidation of bitumens. The studies revealed that the total VOC content increases from about 120 ppm for the raw vacuum residue to about 1900 ppm for so-called bitumen 35/50. The amount of volatile sulfur compounds (VSCs) in the volatile fraction of fumes of oxidized bitumens increases with the degree of oxidation of bitumen and constitutes from 0.34% to 3.66% (w/w). The contribution of volatile nitrogen compounds (VNCs) to total VOC content remains constant for the investigated types of bitumens (from 0.16 to 0.28% (w/w) of total VOCs). The results of these studies can also find use during the selection of appropriate bitumen additives to minimize their malodorousness. The obtained data append the existing knowledge on VOC emission from oxidized bitumens. They should be included in reports on the environmental impact of facilities in which hot bitumen binders are used.

  12. Application of horizontal spiral coil heat exchanger for volatile organic compounds (VOC) emission control.

    PubMed

    Deshpande, P M; Dawande, S D

    2013-04-01

    The petroleum products have wide range of volatility and are required to be stored in bulk. The evaporation losses are significant and it is a economic as well as environmental concern, since evaporative losses of petroleum products cause increased VOC in ambient air. Control of these losses poses a major problem for the storage tank designers. Ever rising cost of petroleum products further adds to the gravity of the problem. Condensation is one of the technologies for reducing volatile organic compounds emissions. Condensation is effected by condenser, which is basically a heat exchanger and the heat exchanger configuration plays an important role. The horizontal spiral coil heat exchanger is a promising configuration that finds an application in VOC control. This paper attempts to understand underlying causes of emissions and analyse the option of horizontal spiral coil heat exchanger as vent condenser.

  13. Environmental guideline for the reduction of volatile organic compound emissions from the plastics processing industry

    SciTech Connect

    1997-12-31

    The purpose of this document is to provide guidance to environmental regulatory agencies, manufacturers, and operators of plastics processing plants regarding the means of reducing emissions containing volatile organic compounds (VOCs) which are released to the environment in the course of production. Sectors covered by the guideline are expanded polystyrene, cellular polyethylene foams, polyvinyl chloride, and reinforced plastics and composites made from thermoset polyester resins. The guideline focuses on the reduction of VOC emissions from processing and clean-up operations, the handling and storage of VOC-containing materials, and the handling and disposal of wastes. The guideline contains material, equipment, process, and operating standards for plastics processing facilities, record keeping and training standards, recommended operating practices, and testing protocols.

  14. Volatile Organic Compound Emissions from Oil and Gas Production Sources: A Pilot Study in Northeastern Oklahoma

    NASA Astrophysics Data System (ADS)

    Ghosh, B.

    2015-12-01

    Volatile organic compounds can be emitted from multiple sources, and as such, it would be useful for a facility to be able to distinguish emissions originating inside battery limits (ISBL) from those originating from external sources. A field campaign of ambient air sampling was conducted at the Phillips 66 Research Center located in Northeastern Oklahoma. The surface measurement campaign included ambient air measurement using two hour and six hour time-integrated canister sampling and measurement of meteorological data. A total of 238 ambient air samples were collected between February and April of 2015 and the concentrations of 55 different hydrocarbons were measured in each of these samples. C2-C5 alkanes were the most dominant hydrocarbons measured during this study with their mean concentrations ranging from 1.5 to 13.6 ppb. The data analysis identified oil and gas production as the primary source of emission. The results and their analysis will be discussed.

  15. Vehicular emission of volatile organic compounds (VOCs) from a tunnel study in Hong Kong

    NASA Astrophysics Data System (ADS)

    Ho, K. F.; Lee, S. C.; Ho, W. K.; Blake, D. R.; Cheng, Y.; Li, Y. S.; Fung, K.; Louie, P. K. K.; Park, D.

    2009-06-01

    Vehicle emissions of VOCs were determined in summer and winter of 2003 at the Shing Mun Tunnel, Hong Kong. One hundred and ten VOCs were quantified in this study. The average concentration of the total measured VOCs at the inlet and outlet of the tunnel were 81 250 pptv and 117 850 pptv, respectively. Among the 110 compounds analyzed, ethene, ethyne and toluene were the most abundant species in the tunnel. The total measured VOC emission factors ranged from 67 mg veh-1 km-1 to 148 mg veh-1 km-1, with an average of 115 mg veh-1 km-1. The five most abundant VOCs observed in the tunnel were, in decreasing order, ethene, toluene, n-butane, propane and i-pentane. These five most abundant species contributed over 38% of the total measured VOCs emitted. The high propane and n-butane emissions were found to be associated with LPG-fueled taxi. And fair correlations were observed between marker species (ethene, i-pentane, n-nonane, BTEX) with fractions of gasoline-fueled or diesel-fueled vehicles. Moreover, ethene, ethyne, and propene are the key species that were abundant in the tunnel but not in gasoline vapors or LPG. In order to evaluate the ozone formation potential emissions in Hong Kong, the maximum increment reactivity is calculated. It was found that about 568 mg of O3 is induced by per vehicle per kilometer traveled. Among them, ethene, propene and toluene contribute most to the ozone-formation reactivity.

  16. Carbonyl compound emissions from passenger cars fueled with methanol/gasoline blends.

    PubMed

    Zhao, Hong; Ge, Yunshan; Hao, Chunxiao; Han, Xiukun; Fu, Mingliang; Yu, Linxiao; Shah, Asad Naeem

    2010-08-01

    Carbonyl compound emissions from two passenger cars fueled with different methanol/gasoline blends (M15 and M100) and operated with three-way catalytic converters (TWC) were investigated. The tests were performed on a chassis dynamometer with constant volume sampling over the New European Driving Cycle (NEDC). Carbonyls were trapped on dinitrophenylhydrazine (DNPH) cartridges. The hydrazones formed on the cartridge were analyzed by means of high-performance liquid chromatography (HPLC) and detected with a variable wavelength detector. The results show that when cars were fueled with methanol/gasoline blends, carbon monoxide (CO) and total hydrocarbon (THC) emissions decreased by 9-21% and 1-55% respectively, while nitrogen oxide (NO(x)) emissions increased by 175-233%. Compared with gasoline vehicles, formaldehyde emissions with M15 and M100 were two and four times higher respectively, and total carbonyls with M15 and M100 increased by 3% and 104% respectively. With the use of the new TWC, both regulated gas pollutants and formaldehyde decreased. The new TWC caused a decrease of 5% and 31% in formaldehyde concentration for M15 and M100, respectively. Specific reactivity (SR) with the new TWC was reduced from 5.92 to 5.72 for M15 and from 7.00 to 6.93 for M100, indicating that M15 and M100 with the new TWC were friendlier to the environment.

  17. Emissions of volatile organic compounds during the decomposition of plant litter

    NASA Astrophysics Data System (ADS)

    Gray, Christopher M.; Monson, Russell K.; Fierer, Noah

    2010-09-01

    Volatile organic compounds (VOCs) are emitted during plant litter decomposition, and such VOCs can have wide-ranging impacts on atmospheric chemistry, terrestrial biogeochemistry, and soil ecology. However, we currently have a limited understanding of the relative importance of biotic versus abiotic sources of these VOCs and whether distinct types of litter emit different types and quantities of VOCs during decomposition. We analyzed VOCs emitted by microbes or by abiotic mechanisms during the decomposition of litter from 12 plant species in a laboratory experiment using proton transfer reaction mass spectrometry (PTR-MS). Net emissions from litter with active microbial populations (non-sterile litters) were between 0 and 11 times higher than emissions from sterile controls over a 20-d incubation period, suggesting that abiotic sources of VOCs are generally less important than biotic sources. In all cases, the sterile and non-sterile litter treatments emitted different types of VOCs, with methanol being the dominant VOC emitted from litters during microbial decomposition, accounting for 78 to 99% of the net emissions. We also found that the types of VOCs released during biotic decomposition differed in a predictable manner among litter types with VOC profiles also changing as decomposition progressed over time. These results show the importance of incorporating both the biotic decomposition of litter and the species-dependent differences in terrestrial vegetation into global VOC emission models.

  18. Deposition of vanadium carbide thin films using compound target sputtering and their field emission

    SciTech Connect

    Liao, M.Y.; Gotoh, Y.; Tsuji, H.; Ishikawa, J.

    2005-09-15

    Vanadium carbide (VC) thin films were deposited on silicon substrates by direct sputtering of a VC target in an argon atmosphere. The structure, composition, and electrical properties of the films were investigated as functions of deposition conditions. The crystallographic structure of the film was strongly related to the argon pressure. VC films with (111) preferred orientation were formed at 2.0 Pa regardless of the substrate temperature examined, while amorphous films were obtained at the lowest pressure of 0.5 Pa. It was shown that carbon segregation within the film was difficult to avoid, but could be suppressed to some degree. To make a full understanding of the compositional variation in compound target sputtering process, deposition of chromium carbide thin films was also performed. Some common mechanisms involved in compound target sputtering process were discussed. Field emission measurements revealed that the VC film is a good electron emitter.

  19. Deposition of vanadium carbide thin films using compound target sputtering and their field emission

    NASA Astrophysics Data System (ADS)

    Liao, M. Y.; Gotoh, Y.; Tsuji, H.; Ishikawa, J.

    2005-09-01

    Vanadium carbide (VC) thin films were deposited on silicon substrates by direct sputtering of a VC target in an argon atmosphere. The structure, composition, and electrical properties of the films were investigated as functions of deposition conditions. The crystallographic structure of the film was strongly related to the argon pressure. VC films with (111) preferred orientation were formed at 2.0 Pa regardless of the substrate temperature examined, while amorphous films were obtained at the lowest pressure of 0.5 Pa. It was shown that carbon segregation within the film was difficult to avoid, but could be suppressed to some degree. To make a full understanding of the compositional variation in compound target sputtering process, deposition of chromium carbide thin films was also performed. Some common mechanisms involved in compound target sputtering process were discussed. Field emission measurements revealed that the VC film is a good electron emitter.

  20. Angular distribution of light emission from compound-eye cornea with conformal fluorescent coating

    NASA Astrophysics Data System (ADS)

    Martín-Palma, Raúl J.; Miller, Amy E.; Pulsifer, Drew P.; Lakhtakia, Akhlesh

    2014-09-01

    The complex morphology of the apposition compound eyes of insects of many species provides them a wide angular field of view. This characteristic makes these eyes attractive for bioreplication as artificial sources of light. The cornea of a blowfly eye was conformally coated with a fluorescent thin film with the aim of achieving wide field-of-view emission. On illumination by shortwave-ultraviolet light, the conformally coated eye emitted visible light whose intensity showed a weaker angular dependence than a fluorescent thin film deposited on a flat surface.

  1. Characterization of odor emission on the working face of landfill and establishing of odorous compounds index.

    PubMed

    Wenjing, Lu; Zhenhan, Duan; Dong, Li; Jimenez, Luis Miguel Caicedo; Yanjun, Liu; Hanwen, Guo; Hongtao, Wang

    2015-08-01

    Temporal variation (seasonal and daily) of odor emission on the working face of a large sanitary landfill in China was characterized through a 2 yearlong case study. Odor pollution was most serious in spring and autumn, while lower odor concentrations were detected in summer and winter. The daily fluctuation of odor concentration on the working face showed that 2:00am, 6:00am, 2:00pm and 10:00pm were the "most probable times" for odor pollution occurrence, which deserves focused attention in odor control projects. Correlations analysis found that 41% of the variance in odor concentrations can be explained by the chemical concentrations of odorous compounds. Moreover, the selection criteria for the index of odorous compounds were also established by evaluating the odor concentration, contribution to odor strength and the frequency of each compound present in all the samples. Ethyl alcohol, α-piene, hydrogen sulfide, dimethyl sulfide, limonene, methyl mercaptan, dimethyl disulfide, and diethyl sulfide comprise the index of odorous compounds on the working face of typical municipal solid waste landfill in China.

  2. NATURAL EMISSIONS OF NON-METHANE VOLATILE ORGANIC COMPOUNDS, CARBON MONOXIDE, AND OXIDES OF NITROGEN FROM NORTH AMERICA. (R825259)

    EPA Science Inventory

    Abstract

    The magnitudes, distributions, controlling processes and uncertainties associated with North American natural emissions of oxidant precursors are reviewed. Natural emissions are responsible for a major portion of the compounds, including non-methane volatile o...

  3. VOLATILE ORGANIC COMPOUND EMISSIONS FROM LATEX PAINT-PART 2. TEST HOUSE STUDIES AND INDOOR AIR QUALITY (IAQ) MODELING

    EPA Science Inventory

    Emission models developed using small chamber data were combined with an Indoor Air Quality (IAQ) model to analyze the impact of volatile organic compound (VOC) emissions from latex paint on indoor environments. Test house experiments were conducted to verify the IAQ model's pred...

  4. Volatile organic compound emissions from wastewater treatment plants in Taiwan: legal regulations and costs of control.

    PubMed

    Cheng, Wen-Hsi; Hsu, Shu-Kang; Chou, Ming-Shean

    2008-09-01

    This study assessed volatile organic compound (VOC) emission characteristics from wastewater treatment plants (WWTPs) in five Taiwanese industrial districts engaged in numerous manufacturing processes, including petrochemical, science-based industry (primarily semiconductors, photo-electronics, electronic products and biological technology), as well as multiple manufacturing processes (primarily pharmaceuticals and paint manufacturing). The most aqueous hydrocarbons dissolved in the wastewater of Taiwanese WWTPs were acetone, acrylonitrile, methylene chloride, and chloroform for the petrochemical districts; acetone, chloroform, and toluene for the science-based districts; and chlorinated and aromatic hydrocarbons for the multiple industrial districts. The aqueous pollutants in the united WWTPs were closely related to the characteristics of the manufacturing plants in the districts. To effectively prevent VOC emissions from the primary treatment section of petrochemical WWTPs, the updated regulations governing VOC emissions were issued by the Taiwanese Environmental Protection Administration in September 2005, legally mandating a seal cover system incorporating venting and air purification equipment. Cost analysis indicates that incinerators with regenerative heat recovery are optimal for treating high VOC concentrations, exceeding 10,000 ppm as CH(4), from the oil separation basins. However, the emission concentrations, ranging from 100 to 1,000 ppm as CH(4) from the other primary treatment facilities and bio-treatment stages, should be collected and then injected into the biological oxidation basins via existing or new blowers. The additional capital and operating costs required to treat the VOC emissions of 1,000 ppm as CH(4) from primary treatment facilities are less than USD 0.1 for per m(3) wastewater treatment capacity.

  5. Technology status report: Off-gas treatment technologies for chlorinated volatile organic compound air emissions

    SciTech Connect

    Rossabi, J.; Haselow, J.S.

    1992-04-15

    The purpose of this document is to review technologies for treatment of air streams that contain chlorinated volatile organic compounds (CVOCS) and to describe a Department of Energy Office of Technology Development program that is planned to demonstrate innovative technologies for the abatement of CVOC emissions. This report describes the first phase of testing of off-gas treatment technologies. At least one more phase of testing is planned. Guidance for the preparation of this document was provided by a predecisional draft outline issued by the Department of Energy`s Office of Technology Development. The report is intended to evaluate the technical and regulatory aspects, public acceptance, and estimated costs of technologies selected for development and testing. These technologies are compared to currently practiced or baseline methods for treatment of CVOC-laden airstreams. A brief overview is provided rather than detailed cost and data comparisons because many of these technologies have not yet been field tested. A description of other promising technologies for the treatment of CVOC emissions is also included. Trichloroethylene (TCE) and perchloroethylene (PCE) were used for industrial cleaning and solvent applications for several decades. These chemicals can be classified as CVOCS. As a result of past standard disposal practices, these types of compounds are persistent groundwater and soil contaminants throughout the United States and the Department of Energy Complex.

  6. Technology status report: Off-gas treatment technologies for chlorinated volatile organic compound air emissions

    SciTech Connect

    Rossabi, J.; Haselow, J.S.

    1992-04-15

    The purpose of this document is to review technologies for treatment of air streams that contain chlorinated volatile organic compounds (CVOCS) and to describe a Department of Energy Office of Technology Development program that is planned to demonstrate innovative technologies for the abatement of CVOC emissions. This report describes the first phase of testing of off-gas treatment technologies. At least one more phase of testing is planned. Guidance for the preparation of this document was provided by a predecisional draft outline issued by the Department of Energy's Office of Technology Development. The report is intended to evaluate the technical and regulatory aspects, public acceptance, and estimated costs of technologies selected for development and testing. These technologies are compared to currently practiced or baseline methods for treatment of CVOC-laden airstreams. A brief overview is provided rather than detailed cost and data comparisons because many of these technologies have not yet been field tested. A description of other promising technologies for the treatment of CVOC emissions is also included. Trichloroethylene (TCE) and perchloroethylene (PCE) were used for industrial cleaning and solvent applications for several decades. These chemicals can be classified as CVOCS. As a result of past standard disposal practices, these types of compounds are persistent groundwater and soil contaminants throughout the United States and the Department of Energy Complex.

  7. Emission of volatile organic compounds from solid waste disposal sites and importance of heat management.

    PubMed

    Urase, Taro; Okumura, Hiroyuki; Panyosaranya, Samerjai; Inamura, Akihiro

    2008-12-01

    The emission of volatile organic compounds (VOCs) from a solid waste disposal site for municipal solid wastes was quantified. The VOCs contained in the landfill gas taken at the site were benzene, toluene, xylenes, ethyl benzenes, and trimethyl benzenes, while the concentrations of chlorinated compounds were very low. The concentration of benzene in the landfill gas samples ranged from below the detection limit to 20 mg m(-3), and the ratio of benzene to toluene ranged from 0.2 to 8. The higher concentrations of VOCs in landfill gas and in leachates were observed with the samples taken at high temperature areas of the target site. Polystyrene plastic waste was identified as one of the sources of VOCs in solid waste disposal sites at a high temperature condition. The appropriate heat management in landfill sites is an important countermeasure to avoid unusually high emission of VOCs because the heat generated by the biodegradation of organic solid wastes may promote the release of VOCs, especially in the case of sites which receive both biodegradable and plastic wastes.

  8. Vehicular emission of volatile organic compounds (VOCs) from a tunnel study in Hong Kong

    NASA Astrophysics Data System (ADS)

    Ho, K. F.; Lee, S. C.; Ho, W. K.; Blake, D. R.; Cheng, Y.; Li, Y. S.; Ho, S. S. H.; Fung, K.; Louie, P. K. K.; Park, D.

    2009-10-01

    Vehicle emissions of volatile organic compounds (VOCs) were determined at the Shing Mun Tunnel, Hong Kong in summer and winter of 2003. One hundred and ten VOCs were quantified in this study. The average concentration of the total measured VOCs at the inlet and outlet of the tunnel were 81 250 pptv and 117 850 pptv, respectively. Among the 110 compounds, ethene, ethyne and toluene were the most abundant species in the tunnel. The total measured VOC emission factors ranged from 67 mg veh-1 km-1 to 148 mg veh-1 km-1, with an average of 115 mg veh-1 km-1. The five most abundant VOCs observed in the tunnel were, in decreasing order, ethene, toluene, n-butane, propane and i-pentane. These five most abundant species contributed over 38% of the total measured VOCs emitted. The high propane and n-butane emissions were found to be associated with liquefied petroleum gas (LPG)-fueled taxis. Fair correlations were observed between marker species (ethene, i-pentane, n-nonane, and benzene, toluene, ethylbenzene and xylenes - BTEX) with fractions of gasoline-fueled or diesel-fueled vehicles. Moreover, ethene, ethyne, and propene are the key species that were abundant in the tunnel but not in gasoline vapors or LPG. The ozone formation potential from the VOCs in Hong Kong was evaluated by the maximum increment reactivity (MIR). It was found to be 568 mg of ozone per vehicle per kilometer traveled. Among them, ethene, propene and toluene contribute most to the ozone-formation reactivity.

  9. Abiotic emissions of methane and reduced organic compounds from organic matter

    NASA Astrophysics Data System (ADS)

    Roeckmann, T.; Keppler, F.; Vigano, I.; Derendorp, L.; Holzinger, R.

    2012-12-01

    Recent laboratory studies show that the important greenhouse gas methane, but also other reduced atmospheric trace gases, can be emitted by abiotic processes from organic matter, such as plants, pure organic compounds and soils. It is very difficult to distinguish abiotic from biotic emissions in field studies, but in laboratory experiments this is easier because it is possible to carefully prepare/sterilize samples, or to control external parameters. For example, the abiotic emissions always show a strong increase with temperature when temperatures are increased to 70C or higher, well above the temperature optimum for bacterial activity. UV radiation has also been clearly shown to lead to emission of methane and other reduced gases from organic matter. Interesting information on the production mechanism has been obtained from isotope studies, both at natural abundance and with isotope labeling. For example, the methoxyl groups of pectin were clearly identified to produce methane. However, analysis of the isotopic composition of methane from natural samples clearly indicates that there must be other molecular mechanisms that lead to methane production. Abiotic methane generation could be a ubiquitous process that occurs naturally at low rates from many different sources.

  10. Volatile Organic Compound Emissions from Dairy Farming and their effect on San Joaquin Valley Air Quality

    NASA Astrophysics Data System (ADS)

    Blake, D. R.; Yang, M.; Meinardi, S.; Krauter, C.; Rowland, F. S.

    2009-05-01

    The San Joaquin Valley Air Pollution Control District of California issued a report identifying dairies as a main source of Volatile Organic Compounds (VOCs). A dairy study funded by the California Air Resources Board commenced shortly after the report was issued. Our University of California Irvine group teamed with California State University Fresno to determine the major sources of VOCs from various dairy operations and from a variety of dairy types. This study identified ethanol and methanol as two gases produced in major quantities throughout the dairies in the San Joaquin valley as by-products of yeast fermentation of silage. Three different types of sampling protocols were employed in order to determine the degree of enhancement of the target oxygenates in the valley air shed. Their sources, emission profiles, and emission rates were determined from whole air samples collected at various locations at the six dairies studied. An assessment of the impact of dairy emissions in the valley was achieved by using data obtained on low altitude NASA DC-8 flights through the valley, and from ground level samples collected though out the valley in a grid like design. Our data suggest that a significant amount of O3 production in the valley may come from methanol, ethanol, and acetaldehyde (a photochemical by-product ethanol oxidation). Our findings indicate that improvement to valley air quality may be obtained by focusing on instituting new silage containment practices and regulations.

  11. Health evaluation of volatile organic compound (VOC) emissions from wood and wood-based materials.

    PubMed

    Jensen, L K; Larsen, A; Mølhave, L; Hansen, M K; Knudsen, B

    2001-01-01

    In this study, the authors describe a method for evaluation of material emissions. The study was based on chemical analysis of emissions from 23 materials representing solid wood and wood-based materials commonly used in furniture, interior furnishings, and building products in Denmark in the 1990s. The authors used the emission chamber testing method to examine the selected materials with a qualitative screening and quantitative determination of volatile organic compounds. The authors evaluated the toxicological effects of all substances identified with chamber testing. Lowest concentration of interest and standard room concentrations were assessed, and the authors calculated an S-value for each wood and wood-based material. The authors identified 144 different chemical substances with the screening analyses, and a total of 84 individual substances were quantified with chamber measurements. The irritative effects dominated at low exposure levels; therefore, the lowest concentration of interest and the S-value were based predominantly on these effects. The S-values were very low for solid ash, oak, and beech. For solid spruce and pine, the determining substances for size of the S-value were delta3-carene, alpha-pinene, and limonene. For the surface-treated wood materials, the S-value reflected the emitted substances from the surface treatment.

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

    PubMed

    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.

  13. Emissions of volatile organic compounds and particulate matter from small-scale peat fires

    NASA Astrophysics Data System (ADS)

    George, I. J.; Black, R.; Walker, J. T.; Hays, M. D.; Tabor, D.; Gullett, B.

    2013-12-01

    Air pollution emitted from peat fires can negatively impact regional air quality, visibility, climate, and human health. Peat fires can smolder over long periods of time and, therefore, can release significantly greater amounts of carbon into the atmosphere per unit area compared to burning of other types of biomass. However, few studies have characterized the gas and particulate emissions from peat burning. To assess the atmospheric impact of peat fires, particulate matter (PM) and volatile organic compounds (VOCs) were quantified from controlled small-scale peat fire experiments. Major carbon emissions (i.e. CO2, CO, methane and total hydrocarbons) were measured during the peat burn experiments. Speciated PM mass was also determined from the peat burns from filter and polyurethane foam samples. Whole air samples were taken in SUMMA canisters and analyzed by gas chromatography-mass spectrometry to measure 82 trace VOCs. Additional gaseous carbonyl species were measured by sampling with dinitrophenylhydrazine-coated cartridges and analyzed with high performance liquid chromatography. VOCs with highest observed concentrations measured from the peat burns were propylene, benzene, chloromethane and toluene. Gas-phase carbonyls with highest observed concentrations included acetaldehyde, formaldehyde and acetone. Emission factors of major pollutants will be compared with recommended values for peat and other biomass burning.

  14. Intermediate Volatility Organic Compound Emissions from On-Road Gasoline Vehicles and Small Off-Road Gasoline Engines.

    PubMed

    Zhao, Yunliang; Nguyen, Ngoc T; Presto, Albert A; Hennigan, Christopher J; May, Andrew A; Robinson, Allen L

    2016-04-19

    Dynamometer experiments were conducted to characterize the intermediate volatility organic compound (IVOC) emissions from a fleet of on-road gasoline vehicles and small off-road gasoline engines. IVOCs were quantified through gas chromatography/mass spectrometry analysis of adsorbent samples collected from a constant volume sampler. The dominant fraction (>80%, on average) of IVOCs could not be resolved on a molecular level. These unspeciated IVOCs were quantified as two chemical classes (unspeciated branched alkanes and cyclic compounds) in 11 retention-time-based bins. IVOC emission factors (mg kg-fuel(-1)) from on-road vehicles varied widely from vehicle to vehicle, but showed a general trend of lower emissions for newer vehicles that met more stringent emission standards. IVOC emission factors for 2-stroke off-road engines were substantially higher than 4-stroke off-road engines and on-road vehicles. Despite large variations in the magnitude of emissions, the IVOC volatility distribution and chemical characteristics were consistent across all tests and IVOC emissions were strongly correlated with nonmethane hydrocarbons (NMHCs), primary organic aerosol and speciated IVOCs. Although IVOC emissions only correspond to approximately 4% of NMHC emissions from on-road vehicles over the cold-start unified cycle, they are estimated to produce as much or more SOA than single-ring aromatics. Our results clearly demonstrate that IVOCs from gasoline engines are an important class of SOA precursors and provide observational constraints on IVOC emission factors and chemical composition to facilitate their inclusion into atmospheric chemistry models.

  15. Measurement of emissions from air pollution sources. 5. C1-C32 organic compounds from gasoline-powered motor vehicles.

    PubMed

    Schauer, James J; Kleeman, Michael J; Cass, Glen R; Simoneit, Bernd R T

    2002-03-15

    Gas- and particle-phase organic compounds present in the tailpipe emissions from an in-use fleet of gasoline-powered automobiles and light-duty trucks were quantified using a two-stage dilution source sampling system. The vehicles were driven through the cold-start Federal Test Procedure (FTP) urban driving cycle on a transient dynamometer. Emission rates of 66 volatile hydrocarbons, 96 semi-volatile and particle-phase organic compounds, 27 carbonyls, and fine particle mass and chemical composition were quantified. Six isoprenoids and two tricyclic terpanes, which are quantified using new source sampling techniques for semi-volatile organic compounds, have been identified as potential tracers for gasoline-powered motor vehicle emissions. A composite of the commercially distributed California Phase II Reformulated Gasoline used in these tests was analyzed by several analytical methods to quantify the gasoline composition, including some organic compounds that are found in the atmosphere as semi-volatile and particle-phase organic compounds. These results allow a direct comparison of the semi-volatile and particle-phase organic compound emissions from gasoline-powered motor vehicles to the gasoline burned by these vehicles. The distribution of n-alkanes and isoprenoids emitted from the catalyst-equipped gasoline-powered vehicles is the same as the distribution of these compounds found in the gasoline used, whereas the distribution of these compounds in the emissions from the noncatalyst vehicles is very different from the distribution in the fuel. In contrast, the distribution of the polycyclic aromatic hydrocarbons and their methylated homologues in the gasoline is significantly different from the distribution of the PAH in the tailpipe emissions from both types of vehicles.

  16. Test methods and reduction of organic pollutant compound emissions from wood-based building and furniture materials.

    PubMed

    Kim, Sumin; Choi, Yoon-Ki; Park, Kyung-Won; Kim, Jeong Tai

    2010-08-01

    This paper reviews different methods for the analysis of formaldehyde and volatile organic compounds (VOCs) from wood-based panel materials for furniture and building interiors and highlights research on reduction of emission from wood-based panels that can adversely affect indoor air quality. In Korea, standard test methods have been developed to determine formaldehyde and VOC emissions from building products, and the Ministry of Environment regulates the use of building materials with pollutant emissions. Desiccator and perforator methods are being used for formaldehyde and the chamber and field and laboratory emission cell (FLEC) methods for VOC and formaldehyde emissions. The VOC analyzer is a suitable pre-test method for application as a total VOC (TVOC) emission test and bake-out is a useful method to reduce TVOC and formaldehyde emissions from furniture materials in indoor environments.

  17. Production of extremely low volatile organic compounds from biogenic emissions: Measured yields and atmospheric implications.

    PubMed

    Jokinen, Tuija; Berndt, Torsten; Makkonen, Risto; Kerminen, Veli-Matti; Junninen, Heikki; Paasonen, Pauli; Stratmann, Frank; Herrmann, Hartmut; Guenther, Alex B; Worsnop, Douglas R; Kulmala, Markku; Ehn, Mikael; Sipilä, Mikko

    2015-06-09

    Oxidation products of monoterpenes and isoprene have a major influence on the global secondary organic aerosol (SOA) burden and the production of atmospheric nanoparticles and cloud condensation nuclei (CCN). Here, we investigate the formation of extremely low volatility organic compounds (ELVOC) from O3 and OH radical oxidation of several monoterpenes and isoprene in a series of laboratory experiments. We show that ELVOC from all precursors are formed within the first minute after the initial attack of an oxidant. We demonstrate that under atmospherically relevant concentrations, species with an endocyclic double bond efficiently produce ELVOC from ozonolysis, whereas the yields from OH radical-initiated reactions are smaller. If the double bond is exocyclic or the compound itself is acyclic, ozonolysis produces less ELVOC and the role of the OH radical-initiated ELVOC formation is increased. Isoprene oxidation produces marginal quantities of ELVOC regardless of the oxidant. Implementing our laboratory findings into a global modeling framework shows that biogenic SOA formation in general, and ELVOC in particular, play crucial roles in atmospheric CCN production. Monoterpene oxidation products enhance atmospheric new particle formation and growth in most continental regions, thereby increasing CCN concentrations, especially at high values of cloud supersaturation. Isoprene-derived SOA tends to suppress atmospheric new particle formation, yet it assists the growth of sub-CCN-size primary particles to CCN. Taking into account compound specific monoterpene emissions has a moderate effect on the modeled global CCN budget.

  18. Soil biochemical properties of grassland ecosystems under anthropogenic emission of nitrogen compounds

    NASA Astrophysics Data System (ADS)

    Kudrevatykh, Irina; Ivashchenko, Kristina; Ananyeva, Nadezhda

    2016-04-01

    Inflow of pollutants in terrestrial ecosystems nowadays increases dramatically, that might be led to disturbance of natural biogeochemical cycles and landscapes structure. Production of nitrogen fertilizers is one of the air pollution sources, namely by nitrogen compounds (NH4+, NO3-, NO2-). Air pollution by nitrogen compounds of terrestrial ecosystems might be affected on soil biochemical properties, which results increasing mineral nitrogen content in soil, changing soil P/N and Al/Ca ratios, and, finally, the deterioration of soil microbial community functioning. The research is focused on the assessment of anthropogenic emission of nitrogen compounds on soil properties of grassland ecosystems in European Russia. Soil samples (Voronic Chernozem Pachic, upper 10 cm mineral layer, totally 10) were taken from grassland ecosystem: near (5-10 m) nitrogen fertilizer factory (NFF), and far from it (20-30 km, served as a control) in Tula region. In soil samples the NH4+ and NO3- (Kudeyarov's photocolorimetric method), P, Ca, Al (X-ray fluorescence method) contents were measured. Soil microbial biomass carbon (Cmic) was analyzed by substrate-induced respiration method. Soil microbial respiration (MR) was assessed by CO2 rate production. Soil microbial metabolic quotient (qCO2) was calculated as MR/Cmic ratio. Near NFF the soil ammonium and nitrate nitrogen contents were a strongly varied, variation coefficient (CV) was 42 and 86This study was supported by Russian Foundation of Basic Research Grant No. 14-04-00098, 15-44-03220, 15-04-00915.

  19. Toxic Volatile Organic Compounds in Environmental Tobacco Smoke:Emission Factors for Modeling Exposures of California Populations

    SciTech Connect

    Daisey, J.M.; Mahanama, K.R.R.; Hodgson, A.T.

    1994-10-01

    The primary objective of this study was to measure emission factors for selected toxic air in environmental tobacco smoke (ETS) using a room-sized environmental chamber. The emissions of 23 volatile organic compounds (VOCs), including 1,3-butadiene, three aldehydes and two vapor-phase N-nitrosarnines were determined for six commercial brands of cigarettes and reference cigarette 1R4F. The commercial brands were selected to represent 62.5% of the cigarettes smoked in California. For each brand, three cigarettes were machine smoked in the chamber. The experiments were conducted over four hours to investigate the effects of aging. Emission factors of the target compounds were also determined for sidestream smoke (SS). For almost all target compounds, the ETS emission factors were significantly higher than the corresponding SS values probably due to less favorable combustion conditions and wall losses in the SS apparatus. Where valid comparisons could be made, the ETS emission factors were generally in good agreement with the literature. Therefore, the ETS emission factors, rather than the SS values, are recommended for use in models to estimate population exposures from this source. The variabilities in the emission factors (pgkigarette) of the selected toxic air contaminants among brands, expressed as coefficients of variation, were 16 to 29%. Therefore, emissions among brands were generally similar. Differences among brands were related to the smoked lengths of the cigarettes and the masses of consumed tobacco. Mentholation and whether a cigarette was classified as light or regular did not significantly affect emissions. Aging was determined not to be a significant factor for the target compounds. There were, however, deposition losses of the less volatile compounds to chamber surfaces.

  20. Supplementation of poultry feeds with dietary zinc and other minerals and compounds to mitigate nitrogen emissions--a review.

    PubMed

    Hunde, Alemu; Patterson, Paul; Ricke, Steven; Kim, Woo Kyun

    2012-06-01

    One of the environmental challenges that the poultry industry has been faced with is ammonia emission from manure. One way to reduce nitrogen excretion and emissions is supplementing dietary trace minerals to inhibit the activity of microbial uricase, a key enzyme converting nitrogen compounds in the manure into ammonia. Several dietary minerals are commercially available as economic alternatives for reducing ammonia emissions in poultry. In this review, we discuss different mineral elements including zinc as feed amendment minerals that could be used to reduce ammonia emission. Issues discussed include potential for inhibiting microbial uricase, dietary supplementation levels, growth performance, toxicity, their influence on manure nitrogen emission, and potential mineral accumulation in soil. In addition, we discuss other minerals and compounds that have the potential to reduce ammonia volatilization by inhibiting microbial uricase and growth of uric acid-utilizing microorganisms.

  1. Emission inventory of primary pollutants and chemical speciation in 2010 for the Yangtze River Delta region, China

    NASA Astrophysics Data System (ADS)

    Fu, Xiao; Wang, Shuxiao; Zhao, Bin; Xing, Jia; Cheng, Zhen; Liu, Huan; Hao, Jiming

    2013-05-01

    We developed a high-resolution emission inventory of primary air pollutants for Yangtze River Delta (YRD) region, which included Shanghai plus 24 cities in the provinces of Jiangsu and Zhejiang. The emissions of SO2, NOX, PM10, PM2.5, NMVOCs and NH3 in the year of 2010 were estimated as 2147 kt, 2776 kt, 1006 kt, 643 kt, 3822 kt and 1439 kt, respectively. Power plants are the largest emission sources for SO2 and NOX, which contributes 44.1% and 37.3% of total SO2 and NOX emissions. Emissions from industrial process accounted for 26.9%, 28.9% and 33.7% of the total PM10, PM2.5 and NMVOCs respectively. Besides, 37.3% of NMVOCs emissions were contributed by solvent use. Livestock and fertilizer application contribute over 90% of NH3 emissions. High emission densities are visible in Shanghai and the area around Tai Lake. This emission inventory includes the speciation of PM2.5 for the YRD region for the first time, which is important to source apportionment and secondary-pollution analysis. In 2010, emissions of three major PM2.5 species, namely OC, EC and sulfate, are 136.9 kt, 75.0 kt and 76.2 kt, respectively. Aromatics and alkanes are the main NMVOC species, accounting for 30.4% and 20.3% of total VOCs. Non-road transportation and biomass burning were main uncertain sources because of a lack of proper activity and emission factor data. Compared with other pollutants, NMVOCs and NH3 have higher uncertainty. From 2000 to 2010, emissions of all pollutants have changed significantly, suggesting that the newly updated and high-resolution emission inventory will be useful for the identification of air pollution sources in YRD.

  2. Emissions of volatile organic compounds (VOCs) from the food and drink industries of the European community

    NASA Astrophysics Data System (ADS)

    Passant, Neil R.; Richardson, Stephen J.; Swannell, Richard P. J.; Gibson, N.; Woodfield, M. J.; van der Lugt, Jan Pieter; Wolsink, Johan H.; Hesselink, Paul G. M.

    Estimates were made of the amounts of volatile organic compounds (VOCs) released into the atmosphere as a result of the industrial manufacture and processing of food and drink in the European Community. The estimates were based on a review of literature sources, industrial and government contacts and recent measurements. Data were found on seven food manufacturing sectors (baking, vegetable oil extraction, solid fat processing, animal rendering, fish meal processing, coffee production and sugar beet processing) and three drink manufacturing sectors (brewing, spirit production and wine making). The principle of a data quality label is advocated to illustrate the authors' confidence in the data, and to highlight areas for further research. Emissions of ethanol from bread baking and spirit maturation were found to be the principle sources. However, significant losses of hexane and large quantities of an ill-defined mixture of partially oxidized hydrocarbons were noted principally from seed oil extraction and the drying of plant material, respectively. This latter mixture included low molecular weight aldehydes, carboxylic acids, ketones, amines and esters. However, the precise composition of many emissions were found to be poorly understood. The total emission from the food and drink industry in the EC was calculated as 260 kt yr -1. However, many processes within the target industry were found to be completely uncharacterized and therefore not included in the overall estimate (e.g. soft drink manufacture, production of animal food, flavourings, vinegar, tea, crisps and other fried snacks). Moreover, the use of data quality labels illustrated the fact that many of our estimates were based on limited data. Hence, further emissions monitoring is recommended from identified sources (e.g. processing of sugar beet, solid fat and fish meal) and from uncharacterized sources.

  3. Emission ratios of anthropogenic volatile organic compounds in northern mid-latitude megacities: Observations versus emission inventories in Los Angeles and Paris

    NASA Astrophysics Data System (ADS)

    Borbon, Agnes; Gilman, J. B.; Kuster, W. C.; Grand, N.; Chevaillier, S.; Colomb, A.; Dolgorouky, C.; Gros, V.; Lopez, M.; Sarda-Esteve, R.; Holloway, J.; Stutz, J.; Petetin, H.; McKeen, S.; Beekmann, M.; Warneke, C.; Parrish, D. D.; Gouw, J. A.

    2013-02-01

    Ground-based and airborne volatile organic compound (VOC) measurements in Los Angeles, California, and Paris, France, during the Research at the Nexus of Air Quality and Climate Change (CalNex) and Megacities: Emissions, Urban, Regional and Global Atmospheric Pollution and Climate Effects, and Integrated Tools for Assessment and Mitigation (MEGAPOLI) campaigns, respectively, are used to examine the spatial variability of the composition of anthropogenic VOC urban emissions and to evaluate regional emission inventories. Two independent methods that take into account the effect of chemistry were used to determine the emission ratios of anthropogenic VOCs (including anthropogenic isoprene and oxygenated VOCs) over carbon monoxide (CO) and acetylene. Emission ratios from both methods agree within ±20%, showing the reliability of our approach. Emission ratios for alkenes, alkanes, and benzene are fairly similar between Los Angeles and Paris, whereas the emission ratios for C7-C9 aromatics in Paris are higher than in Los Angeles and other French and European Union urban areas by a factor of 2-3. The results suggest that the emissions of gasoline-powered vehicles still dominate the hydrocarbon distribution in northern mid-latitude urban areas, which disagrees with emission inventories. However, regional characteristics like the gasoline composition could affect the composition of hydrocarbon emissions. The observed emission ratios show large discrepancies by a factor of 2-4 (alkanes and oxygenated VOC) with the ones derived from four reference emission databases. A bias in CO emissions was also evident for both megacities. Nevertheless, the difference between measurements and inventory in terms of the overall OH reactivity is, in general, lower than 40%, and the potential to form secondary organic aerosols (SOA) agrees within 30% when considering volatile organic emissions as the main SOA precursors.

  4. Field Derived Emission Factors For Formaldehyde and other Volatile Organic Compounds in FEMA Temporary Housing Units

    SciTech Connect

    Parthasarathy, Srinandini; Maddalena, Randy L.; Russell, Marion L.; Apte, Michael G.

    2010-10-01

    Sixteen previously occupied temporary housing units (THUs) were studied to assess emissions of volatile organic compounds. The whole trailer emission factors wereevaluated for 36 VOCs including formaldehyde. Indoor sampling was carried out in the THUs located in Purvis staging yard in Mississippi, USA. Indoor temperature andrelative humidity (RH) were also measured in all the trailers during sampling. Indoor temperatures were varied (increased or decreased) in a selection of THUs using theheating, ventilation and air conditioning (HVAC) systems. Indoor temperatures during sampling ranged from 14o C to 33o C, and relative humidity (RH) varied between 35percentand 74percent. Ventilation rates were increased in some trailers using bathroom fans and vents during some of the sampling events. Ventilation rates measured during some aselection of sampling events varied from 0.14 to 4.3 h-1. Steady state indoor formaldehyde concentrations ranged from 10 mu g-m-3 to 1000 mu g-m-3. The formaldehyde concentrations in the trailers were of toxicological significance. The effects of temperature, humidity and ventilation rates were also studied. A linearregression model was built using log of percentage relative humidity, inverse of temperature (in K-1), and inverse log ACH as continuous independent variables, trailermanufacturer as a categorical independent variable, and log of the chemical emission factors as the dependent variable. The coefficients of inverse temperature, log relativehumidity, log inverse ACH with log emission factor were found to be statistically significant for all the samples at the 95percent confidence level. The regression model wasfound to explain about 84percent of the variation in the dependent variable. Most VOC concentrations measured indoors in the Purvis THUs were mostly found to be belowvalues reported in earlier studies by Maddalena et al.,1,2 Hodgson et al.,3 and Hippelein4. Emissions of TMPB-DIB (a plasticizer found in vinyl products) were found

  5. Volatile organic compound concentrations and emission rates measured over one year in a new manufactured house

    SciTech Connect

    Hodgson, Alfred T.; Nabinger, Steven J.; Persily, Andrew K.

    2004-09-01

    A study to measure indoor concentrations and emission rates of volatile organic compounds (VOCs), including formaldehyde, was conducted in a new, unoccupied manufactured house installed at the National Institute of Standards and Technology (NIST) campus. The house was instrumented to continuously monitor indoor temperature and relative humidity, heating and air conditioning system operation, and outdoor weather. It also was equipped with an automated tracer gas injection and detection system to estimate air change rates every 2 h. Another automated system measured indoor concentrations of total VOCs with a flame ionization detector every 30 min. Active samples for the analysis of VOCs and aldehydes were collected indoors and outdoors on 12 occasions from August 2002 through September 2003. Individual VOCs were quantified by thermal desorption to a gas chromatograph with a mass spectrometer detector (GC/MS). Formaldehyde and acetaldehyde were quantified by high performance liquid chromatography (HPLC). Weather conditions changed substantially across the twelve active sampling periods. Outdoor temperatures ranged from 7 C to 36 C. House air change rates ranged from 0.26 h{sup -1} to 0.60 h{sup -1}. Indoor temperature was relatively constant at 20 C to 24 C for all but one sampling event. Indoor relative humidity (RH) ranged from 21% to 70%. The predominant and persistent indoor VOCs included aldehydes (e.g., formaldehyde, acetaldehyde, pentanal, hexanal and nonanal) and terpene hydrocarbons (e.g., a-pinene, 3-carene and d-limonene), which are characteristic of wood product emissions. Other compounds of interest included phenol, naphthalene, and other aromatic hydrocarbons. VOC concentrations were generally typical of results reported for other new houses. Measurements of total VOCs were used to evaluate short-term changes in indoor VOC concentrations. Most of the VOCs probably derived from indoor sources. However, the wall cavity was an apparent source of

  6. Emissive cyanide-bridged bimetallic compounds as building blocks for polymeric antennae.

    PubMed

    Cadranel, Alejandro; Aramburu Trošelj, Bruno M; Yamazaki, Shiori; Alborés, Pablo; Kleiman, Valeria D; Baraldo, Luis M

    2013-12-28

    A series of cyanide-bridged bimetallic compounds of the general formula [Ru(L)(bpy)(μ-NC)(M)](2-/-/2+) (L = tpy, 2,2'-6',2''-terpyridine, or tpm, tris(1-pyrazolyl)methane, bpy = 2,2'-bipyridine, M = Ru(II)(CN)5, Os(III)(CN)5, Os(II)(CN)5, Ru(II)(py)4(CN), py = pyridine) have been synthesized and fully characterized. Most of them present MLCT emission (λ = 690-730 nm, Φ = 10(-3)-10(-4)) and their photophysical properties resemble the ones of the respective mononuclear Ru(L)(bpy) species. The exception is when M is Os(III)(CN)5, where an intramolecular electron transfer quenching mechanism is proposed. The conditions that should be met for avoiding the reductive or oxidative quenching of the excited state are also discussed.

  7. Tracing CO2 fluxes and plant volatile organic compound emissions by stable isotopes

    NASA Astrophysics Data System (ADS)

    Werner, Christiane; Wegener, Frederik; Jardine, Kolby

    2014-05-01

    Plant metabolic processes exert a large influence on global climate and air quality through the emission of the greenhouse gas CO2 and volatile organic compounds (VOCs). Despite the enormous importance, processes controlling plant carbon allocation into primary and secondary metabolism, such as respiratory CO2 emission and VOC synthesis, remains unclear. The vegetation exerts a large isotopic imprint on the atmosphere through both, photosynthetic carbon isotope discrimination and fractionation during respiratory CO2 release (δ13Cres). While the former is well understood, many processes driving carbon isotope fractionation during respiration are unknown1. There are striking differences in variations of δ13Cres between plant functional groups, which have been proposed to be related to carbon partitioning in the metabolic branching points of the respiratory pathways and secondary metabolism, which are linked via a number of interfaces including the central metabolite pyruvate2. Notably, it is a known substrate in a large array of secondary pathways leading to the biosynthesis of many volatile organic compounds (VOCs), such as volatile isoprenoids, oxygenated VOCs, aromatics, fatty acid oxidation products, which can be emitted by plants. Here we investigate if carbon isotope fractionation in light and dark respired CO2 is associated with VOC emissions in the atmosphere. Specifically, we hypothesize that a high carbon flux through the pyruvate into various VOC synthesis pathways is associated with a pronounced 13C-enrichment of respired CO2 above the putative substrate, as it involves the decarboxylation of the 13C-enriched C-1 from pyruvate. Based on simultaneous real-time measurements of stable carbon isotope composition of branch respired CO2 (CRDS) and VOC fluxes (PTR-MS) we traced carbon flow into these pathways by pyruvate positional labeling. We demonstrated that in a Mediterranean shrub the 13C-enriched C-1 from pyruvate is released in substantial amounts as

  8. Emissions of volatile organic compounds from building materials and consumer products

    NASA Astrophysics Data System (ADS)

    Wallace, Lance A.; Pellizzari, Edo; Leaderer, Brian; Zelon, Harvey; Sheldon, Linda

    EPA's TEAM Study of personal exposure to volatile organic compounds (VOC) in air and drinking water of 650 residents of seven U.S. cities resulted in the identification of a number of possible sources encountered in peoples' normal daily activities and in their homes. A follow-up EPA study of publicaccess buildings implicated other potential sources of exposure. To learn more about these potential sources, 15 building materials and common consumer products were analyzed using a headspace technique to detect organic emissions and to compare relative amounts. About 10-100 organic compounds were detected offgassing from each material. Four mixtures of materials were then chosen for detailed study: paint on sheetrock; carpet and carpet glue; wallpaper and adhesives; cleansers and a spray pesticide. The materials were applied as normally used, allowed to age 1 week (except for the cleansers and pesticides, which were used normally during the monitoring period), and placed in an environmentally controlled chamber. Organic vapors were collected on Tenax-GC over a 4-h period and analyzed by GC-MS techniques. Emission rates and chamber concentrations were calculated for 17 target chemicals chosen for their toxic, carcinogenic or mutagenic properties. Thirteen of the 17 chemicals were emitted by one or more of the materials. Elevated concentrations of chloroform, carbon tetrachloride, 1,1,1-trichloroethane, n-decane, n-undecane, p-dichlorobenzene, 1,2-dichloroethane and styrene were produced by the four mixtures of materials tested. For some chemicals, these amounts were sufficient to account for a significant fraction of the elevated concentrations observed in previous indoor air studies. We conclude that common materials found in nearly every home and place of business may cause elevated exposures to toxic chemicals.

  9. Laboratory measurements of emissions of nonmethane volatile organic compounds from biomass burning in Chinese crop residues

    NASA Astrophysics Data System (ADS)

    Inomata, S.; Tanimoto, H.; PAN, X.; Taketani, F.; Komazaki, Y.; Miyakawa, T.; Kanaya, Y.; Wang, Z.

    2014-12-01

    The emission factors (EFs) of volatile organic compounds (VOCs) from the burning of Chinese crop residue were investigated as a function of modified combustion efficiency by the laboratory experiments. The VOCs including acetonitrile, aldehydes/ketones, furan, and aromatic hydrocarbons were monitored by proton-transfer-reaction mass spectrometry. Two samples, wheat straw and rape plant, were burned in dry conditions and for some experiments wheat straw was burned under wet conditions. We compared the present data to the field data reported by Kudo et al. [2014]. The agreement between the field and laboratory data was obtained for aromatics for relatively more smoldering data of dry samples but the field data were slightly underestimated compared with the laboratory data for oxygenated VOCs (OVOCs) and acetonitrile. When the EFs from the burning of wet samples were investigated, the underestimations for OVOCs and acetonitrile were improved compared with the data of dry samples. It may be a property of the burning of crop residue in the region of high temperature and high humidity that some inside parts of piled crop residue and/or the crop residue facing on the ground are still wet. But the ratios for acetic acid/glycolaldehyde was still lower than 1. This may suggest that strong loss processes of acetic acid/glycolaldehyde are present in the fresh plume.Kudo S., H. Tanimoto, S. Inomata, S. Saito, X. L. Pan, Y. Kanaya, F. Taketani, Z. F. Wang, H. Chen, H. Dong, M. Zhang, and K. Yamaji (2014), Emissions of nonmethane volatile organic compounds from open crop residue burning in Yangtze River Delta region, China, J. Geophys. Res. Atmos., 119, 7684-7698, doi: 10.1002/2013JD021044.

  10. Enhanced Volatile Organic Compounds emissions and organic aerosol mass increase the oligomer content of atmospheric aerosols.

    PubMed

    Kourtchev, Ivan; Giorio, Chiara; Manninen, Antti; Wilson, Eoin; Mahon, Brendan; Aalto, Juho; Kajos, Maija; Venables, Dean; Ruuskanen, Taina; Levula, Janne; Loponen, Matti; Connors, Sarah; Harris, Neil; Zhao, Defeng; Kiendler-Scharr, Astrid; Mentel, Thomas; Rudich, Yinon; Hallquist, Mattias; Doussin, Jean-Francois; Maenhaut, Willy; Bäck, Jaana; Petäjä, Tuukka; Wenger, John; Kulmala, Markku; Kalberer, Markus

    2016-10-13

    Secondary organic aerosol (SOA) accounts for a dominant fraction of the submicron atmospheric particle mass, but knowledge of the formation, composition and climate effects of SOA is incomplete and limits our understanding of overall aerosol effects in the atmosphere. Organic oligomers were discovered as dominant components in SOA over a decade ago in laboratory experiments and have since been proposed to play a dominant role in many aerosol processes. However, it remains unclear whether oligomers are relevant under ambient atmospheric conditions because they are often not clearly observed in field samples. Here we resolve this long-standing discrepancy by showing that elevated SOA mass is one of the key drivers of oligomer formation in the ambient atmosphere and laboratory experiments. We show for the first time that a specific organic compound class in aerosols, oligomers, is strongly correlated with cloud condensation nuclei (CCN) activities of SOA particles. These findings might have important implications for future climate scenarios where increased temperatures cause higher biogenic volatile organic compound (VOC) emissions, which in turn lead to higher SOA mass formation and significant changes in SOA composition. Such processes would need to be considered in climate models for a realistic representation of future aerosol-climate-biosphere feedbacks.

  11. Determination of volatile organic compound emissions and ozone formation from spraying solvent-based pesticides.

    PubMed

    Kumar, Anuj; Howard, Cody J; Derrick, Doniche; Malkina, Irina L; Mitloehner, Frank M; Kleeman, Michael J; Alaimo, Christopher P; Flocchini, Robert G; Green, Peter G

    2011-01-01

    Large-scale agricultural activities have come under scrutiny for possible contributions to the emission of ozone precursors. The San Joaquin Valley (SJV) of California is an area with intense agricultural activity that exceeds the federal ozone standards for more than 30 to 40 d yr(-1) and the more stringent state standards for more than 100 d yr(-1). Pesticides are used widely in both agricultural and residential subregions of the SJV, but the largest use, by weight of "active ingredient," is in agriculture. The objective of the study was to determine the role of pesticide application on airborne volatile organic compounds (VOC) concentrations and ozone formation in the SJV. The ozone formation from the pesticide formulation sprayed on commercial orchards was studied using two transportable smog chambers at four application sites during the summers of 2007 and 2008. In addition to the direct measurements of ozone formation, airborne VOC concentrations were measured before and after pesticide spraying using canister and sorbent tube sampling techniques. Soil VOC concentrations were also measured to understand the distribution of VOCs between different environmental compartments. Numerous VOCs were detected in the air and soil samples throughout the experiment but higher molecular weight aromatic hydrocarbons were the primary compounds observed in elevated concentrations immediately after pesticide spraying. Measurements indicate that the ozone concentration formed by VOC downwind of the orchard may increase up to 15 ppb after pesticide application, with a return back to prespray levels after 1 to 2 d.

  12. Enhanced Volatile Organic Compounds emissions and organic aerosol mass increase the oligomer content of atmospheric aerosols

    NASA Astrophysics Data System (ADS)

    Kourtchev, Ivan; Giorio, Chiara; Manninen, Antti; Wilson, Eoin; Mahon, Brendan; Aalto, Juho; Kajos, Maija; Venables, Dean; Ruuskanen, Taina; Levula, Janne; Loponen, Matti; Connors, Sarah; Harris, Neil; Zhao, Defeng; Kiendler-Scharr, Astrid; Mentel, Thomas; Rudich, Yinon; Hallquist, Mattias; Doussin, Jean-Francois; Maenhaut, Willy; Bäck, Jaana; Petäjä, Tuukka; Wenger, John; Kulmala, Markku; Kalberer, Markus

    2016-10-01

    Secondary organic aerosol (SOA) accounts for a dominant fraction of the submicron atmospheric particle mass, but knowledge of the formation, composition and climate effects of SOA is incomplete and limits our understanding of overall aerosol effects in the atmosphere. Organic oligomers were discovered as dominant components in SOA over a decade ago in laboratory experiments and have since been proposed to play a dominant role in many aerosol processes. However, it remains unclear whether oligomers are relevant under ambient atmospheric conditions because they are often not clearly observed in field samples. Here we resolve this long-standing discrepancy by showing that elevated SOA mass is one of the key drivers of oligomer formation in the ambient atmosphere and laboratory experiments. We show for the first time that a specific organic compound class in aerosols, oligomers, is strongly correlated with cloud condensation nuclei (CCN) activities of SOA particles. These findings might have important implications for future climate scenarios where increased temperatures cause higher biogenic volatile organic compound (VOC) emissions, which in turn lead to higher SOA mass formation and significant changes in SOA composition. Such processes would need to be considered in climate models for a realistic representation of future aerosol-climate-biosphere feedbacks.

  13. Enhanced Volatile Organic Compounds emissions and organic aerosol mass increase the oligomer content of atmospheric aerosols

    PubMed Central

    Kourtchev, Ivan; Giorio, Chiara; Manninen, Antti; Wilson, Eoin; Mahon, Brendan; Aalto, Juho; Kajos, Maija; Venables, Dean; Ruuskanen, Taina; Levula, Janne; Loponen, Matti; Connors, Sarah; Harris, Neil; Zhao, Defeng; Kiendler-Scharr, Astrid; Mentel, Thomas; Rudich, Yinon; Hallquist, Mattias; Doussin, Jean-Francois; Maenhaut, Willy; Bäck, Jaana; Petäjä, Tuukka; Wenger, John; Kulmala, Markku; Kalberer, Markus

    2016-01-01

    Secondary organic aerosol (SOA) accounts for a dominant fraction of the submicron atmospheric particle mass, but knowledge of the formation, composition and climate effects of SOA is incomplete and limits our understanding of overall aerosol effects in the atmosphere. Organic oligomers were discovered as dominant components in SOA over a decade ago in laboratory experiments and have since been proposed to play a dominant role in many aerosol processes. However, it remains unclear whether oligomers are relevant under ambient atmospheric conditions because they are often not clearly observed in field samples. Here we resolve this long-standing discrepancy by showing that elevated SOA mass is one of the key drivers of oligomer formation in the ambient atmosphere and laboratory experiments. We show for the first time that a specific organic compound class in aerosols, oligomers, is strongly correlated with cloud condensation nuclei (CCN) activities of SOA particles. These findings might have important implications for future climate scenarios where increased temperatures cause higher biogenic volatile organic compound (VOC) emissions, which in turn lead to higher SOA mass formation and significant changes in SOA composition. Such processes would need to be considered in climate models for a realistic representation of future aerosol-climate-biosphere feedbacks. PMID:27733773

  14. Sampling and Analysis of Organophosphorus Compounds on a Thermoelectric Cold Plate Using Fourier Transform Infrared Emission Spectroscopy

    DTIC Science & Technology

    1990-07-01

    natural component of the earth’s atmosphere and is also a pollutant formed in urban air along with oxides of nitrogen and sulfur. Some organic...was applied neat. 3. RESULTS 3.1 Infrared Emission Measurements . Initially for the emission measurements , a thin film of the pesticide phorate was...tor personnel in conjunction with CRDEC scientists. This research addressed the sampling of organophosphorus compounds from the air and their detection

  15. Near-Roadway Emission of Reactive Nitrogen Compounds and Other Non-Criteria Pollutants at a Southern California Freeway Site

    NASA Astrophysics Data System (ADS)

    Moss, J. A.; Baum, M.; Castonguay, A. E.; Aguirre, V., Jr.; Pesta, A.; Fanter, R. K.; Anderson, M.

    2015-12-01

    Emission control systems in light-duty motor vehicles (LDMVs) have played an important role in improving regional air quality by dramatically reducing the concentration of criteria pollutants (carbon monoxide, hydrocarbons, and nitrogen oxides) in exhaust emissions. Unintended side-reactions occurring on the surface of three-way catalysts may lead to emission of a number of non-criteria pollutants whose identity and emission rates are poorly understood. A series of near-roadway field studies conducted between 2009-2015 has investigated LDMV emissions of these pollutants with unprecedented depth of coverage, including reactive nitrogen compounds (NH3, amines, HCN, HONO, and HNO3), organic peroxides, and carbonyl compounds (aldehydes, ketones, and carboxylic acids). Methods to collect these pollutants using mist chambers, annular denuders, impingers, and solid-phase cartridges and quantify their concentration using GC-MS, LC-MS/MS, IC, and colorimetry were developed and validated in the laboratory and field. These methods were subsequently used in near-roadway field studies where the concentrations of the target compounds integrated over 1-4 hour blocks were measured at the edge of a freeway and at a background site 140 m from the roadway. Concentrations followed a steep decreasing gradient from the freeway to the background site. Emission factors (pollutant mass emitted per mass fuel consumed) were calculated by carbon mass balance using the difference in concentration measured between the freeway and background sites for the emitted pollutant and CO2 as a measure of carbon mass in the vehicle exhaust. The significance of these results will be discussed in terms of emissions inventories in the South Coast Air Basin of California, emission trends at this site over the period of 2009-2015, and for NH3, emission measurements conducted by our group and others over the period 2000-2015.

  16. Online measurements of the emissions of intermediate-volatility and semi-volatile organic compounds from aircraft

    NASA Astrophysics Data System (ADS)

    Cross, E. S.; Hunter, J. F.; Carrasquillo, A. J.; Franklin, J. P.; Herndon, S. C.; Jayne, J. T.; Worsnop, D. R.; Miake-Lye, R. C.; Kroll, J. H.

    2013-03-01

    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.

  17. Online measurements of the emissions of intermediate-volatility and semi-volatile organic compounds from aircraft

    NASA Astrophysics Data System (ADS)

    Cross, E. S.; Hunter, J. F.; Carrasquillo, A. J.; Franklin, J. P.; Herndon, S. C.; Jayne, J. T.; Worsnop, D. R.; Miake-Lye, R. C.; Kroll, J. H.

    2013-08-01

    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.

  18. Intermediate Volatility Organic Compound Emissions from On-Road Diesel Vehicles: Chemical Composition, Emission Factors, and Estimated Secondary Organic Aerosol Production.

    PubMed

    Zhao, Yunliang; Nguyen, Ngoc T; Presto, Albert A; Hennigan, Christopher J; May, Andrew A; Robinson, Allen L

    2015-10-06

    Emissions of intermediate-volatility organic compounds (IVOCs) from five on-road diesel vehicles and one off-road diesel engine were characterized during dynamometer testing. The testing evaluated the effects of driving cycles, fuel composition and exhaust aftertreatment devices. On average, more than 90% of the IVOC emissions were not identified on a molecular basis, instead appearing as an unresolved complex mixture (UCM) during gas-chromatography mass-spectrometry analysis. Fuel-based emissions factors (EFs) of total IVOCs (speciated + unspeciated) depend strongly on aftertreatment technology and driving cycle. Total-IVOC emissions from vehicles equipped with catalyzed diesel particulate filters (DPF) are substantially lower (factor of 7 to 28, depending on driving cycle) than from vehicles without any exhaust aftertreatment. Total-IVOC emissions from creep and idle operations are substantially higher than emissions from high-speed operations. Although the magnitude of the total-IVOC emissions can vary widely, there is little variation in the IVOC composition across the set of tests. The new emissions data are combined with published yield data to investigate secondary organic aerosol (SOA) formation. SOA production from unspeciated IVOCs is estimated using surrogate compounds, which are assigned based on gas-chromatograph retention time and mass spectral signature of the IVOC UCM. IVOCs contribute the vast majority of the SOA formed from exhaust from on-road diesel vehicles. The estimated SOA production is greater than predictions by previous studies and substantially higher than primary organic aerosol. Catalyzed DPFs substantially reduce SOA formation potential of diesel exhaust, except at low speed operations.

  19. Effects of gasoline aromatic content on emissions of volatile organic compounds and aldehydes from a four-stroke motorcycle.

    PubMed

    Yao, Yung-Chen; Tsai, Jiun-Horng

    2013-01-01

    A new four-stroke carburettor motorcycle engine without any engine adjustments was used to study the impact of fuel aromatic content on the exhaust emissions of organic air pollutants (volatile organic compounds and carbonyls). Three levels of aromatic content, i.e. 15, 25, and 50% (vol.) aromatics mixed with gasoline were tested. The emissions of aromatic fuel were compared with those of commercial unleaded gasoline. The results indicated that the A 15 (15 vol% aromatics in gasoline) fuel exhibited the greatest total organic emission improvement among these three aromatic fuels as compared with commercial gasoline, reaching 59%. The highest emission factors of alkanes, alkenes, and carbonyl groups appeared in the reference fuel (RF) among all of the test fuels. A 15 showed the highest emission reduction in alkanes (73%), aromatics (36%), and carbonyls (28%), as compared to those of the RF. The highest emission reduction ofalkenes was observed when using A25 as fuel. A reduction in fuel aromatic content from 50 to 25 and 15 vol% in gasoline decreased benzene and toluene emissions, but increased the aldehyde emissions. In general, the results showed that the highest emission reductions for the most of measured organic pollutants appeared when using A 15 as the fuel.

  20. AN IMPROVED MODEL FOR ESTIMATING EMISSIONS OF VOLATILE ORGANIC COMPOUNDS FROM FORESTS IN THE EASTERN UNITED STATES (Journal)

    EPA Science Inventory

    Regional estimates of biogenic volatile organic compound (BVOC) emissions are important inputs for models of atmospheric chemistry and carbon budgets. Since forests are the primary emitters of BVOCs, it is important to develop reliable estimates of their areal coverage and BVOC e...

  1. Semivolatile organic compound emissions from heavy-duty trucks operating on diesel and bio-diesel fuel blends

    EPA Science Inventory

    This study measured semivolatile organic compounds (SVOCs) in particle matter (PM) emitted from three heavy-duty trucks equipped with modern after-treatment technologies. Emissions testing was conducted as described by the George et al. VOC study also presented as part of this se...

  2. Volatile Organic Compound (VOC) emissions from feedlot pen surface materials as affected by within pen location, moisture, and temperature

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A laboratory study was conducted to evaluate the effects of pen location, moisture, and temperature on emissions of volatile organic compounds (VOC) from surface materials obtained from feedlot pens where beef cattle were fed a diet containing 30% wet distillers grain plus solubles. Surface material...

  3. An Evaluation of Hazardous Air Pollutants and Volatile Organic Compound Emissions from Tank Barges in Memphis, TN

    EPA Science Inventory

    Many urban centers have population centers near river ports, which may be affected by volatile organic compound (VOC) and hazardous air pollutant (HAP) emissions from tank barge traffic. This study will examine Memphis, Tennessee and West Memphis, Arkansas. Both cities (located ...

  4. CAPILLARY GAS CHROMATOGRAPHY-ATOMIC EMISSION DETECTION METHOD FOR THE DETERMINATION OF PENTYLATED ORGANOTIN COMPOUNDS: INTERLABORATORY STUDY

    EPA Science Inventory

    A capillary gas chromatography-atomic emission detection (GC-AED) method was developed for the U. S. Environmental Protection Agency's Environmental Monitoring Systems Laboratory in Las Vegas, NV, for determination of selected organotin compounds. Here we report on an interlabora...

  5. BIOGENIC VOLATILE ORGANIC COMPOUND EMISSIONS (BVOCS) I. IDENTIFICATIONS FROM THREE CONTINENTAL SITES IN THE U.S.

    EPA Science Inventory

    Vegetation composition and biomass were surveyed for three specific sites in Atlanta, GA; near Rhinelander, WI; and near Hayden, CO. At each research site, emissions of biogenic volatile organic compounds (BVOCs) from the dominant vegetation species were sampled by enclosing bran...

  6. A NONSTEADY-STATE ANALYTICAL MODEL TO PREDICT GASEOUS EMISSIONS OF VOLATILE ORGANIC COMPOUNDS FROM LANDFILLS. (R825689C072)

    EPA Science Inventory

    Abstract

    A general mathematical model is developed to predict emissions of volatile organic compounds (VOCs) from hazardous or sanitary landfills. The model is analytical in nature and includes important mechanisms occurring in unsaturated subsurface landfill environme...

  7. Ozone Formation Potentials from Different Anthropogenic Emission Sources of Volatile Organic Compounds in California's South Coast Air Basin

    NASA Astrophysics Data System (ADS)

    Chen, J.; Luo, D.; Croes, B.

    2010-12-01

    Different volatile organic compounds (VOC) exhibit different propensities for ozone formation. Two approaches were used to study the relative ozone formation potentials (source reactivities) of different anthropogenic VOC emission source categories in California’s South Coast Air Basin (SoCAB). The first approach combined emission speciation profiles for total organic gases (TOG) with maximum incremental reactivity (MIR) scales for VOC species. The second approach quantified ozone impacts from different sources by performing 3-dimensional air quality model sensitivity analyses involving increased TOG emissions from particular sources. The source reactivities for 58 VOC emission categories in SoCAB derived from these two approaches agree reasonably well (R2 = ~0.9). Both approaches revealed the two emissions source types with the highest TOG reactivity were mobile sources and managed forest burning. Also, a reactivity-based TOG emission inventory for SoCAB in 2005 was produced by combining the source reactivities from both approaches with TOG emissions from anthropogenic source categories. The top five reactivity-based source categories are: light-duty passenger cars, off-road equipments, consumer products, light-duty trucks, and recreational boats. This is in contrast to the mass-based TOG emission inventory, which indicates that farming operations (mainly from animal waste) was one of the five largest mass-based anthropogenic TOG emission sources. Compared to the mass-based TOG emission inventory, the reactivity-based TOG emission inventory more appropriately represents the ozone formation potentials from emission sources, and highlights those sources that should be targeted for future regulations.

  8. Biological Volatile Organic Compounds (BVOCs) emissions from the planktonic diatom Thalassiosira pseudonana

    NASA Astrophysics Data System (ADS)

    Evans, T.; Mak, J. E.

    2009-12-01

    Understanding the behavior of biological volatile organic compounds (BVOCs) is important because in the atmosphere they can be highly reactive, have short residence times, and serve as precursors to aerosol particles. . At present the origin and quantities of BVOCs are still unknown. Phytoplankton and oceanic microbes have been considered an insignificant source of BVOCs until the last few years. In this study we investigated the importance of the diatom Thalassiosira pseudonana in the release of BVOCs into the atmosphere The focus of this study was to determine: a.) BVOC production that would occur over thirty days in which the species would experience initial growth, followed by cell lysis; and b.) to address the effect of nutrient limitation on VOC emissions. Our hypothesis was that the greatest formation of BVOCs would occur during cell lysis due to the breaking of cell membranes and release of organic matter into the surface water which could then undergo photolysis. Media was grown in filtered coastal water and inoculated with T. pseudonana. Samples were taken with a trap and purge system attached to a gas chromatograph with flame ionization detector (Hewlett Packard GC-FID 6890). Two main compounds were observed: isoprene and dimethyl sulfide (DMS). These two compounds have been linked to form aerosols in the atmosphere. After cell lysis had occurred, the production of isoprene remained constant throughout the entire life cycle at approximately 1.55x 10-19 moles/cell/hr. For DMS an increase in production occurred after cell lysis with a maximum production of 2.24 x 10-17 moles/cell/hr on the 25th day of the growth cycle. Key nutrients such as phosphate, nitrate and silica were limited during a series of incubations. BVOC production decreased as nutrient limitation occurred. A secondary VOC, 2, 3-dimethyl pentane (2, 3-DMP), was observed as a by-product of the environmental media. 2, 3-DMP may be produced during the breakdown of vitamin B12 within the F/2

  9. Volatile Organic Compound (VOC) Emissions from Dairy Cows and Their Waste

    NASA Astrophysics Data System (ADS)

    Shaw, S.; Holzinger, R.; Mitloehner, F.; Goldstein, A.

    2005-12-01

    Biogenic VOCs are typically defined as those directly emitted from plants, but approximately 6% of global net primary production is consumed by cattle that carry out enteric fermentation and then emit VOCs that could also be considered biogenic. Current regulatory estimates suggest that dairy cattle in central California emit VOCs at rates comparable to those from passenger vehicles in the region, and thus contribute significantly to the extreme non-attainment of ozone standards there. We report PTR-MS measurements of ammonia and VOCs, and cavity-enhanced-absorption gas analyzer (Los Gatos Research, Inc.) measurements of CH4, emitted from dairy cattle in various stages of pregnancy/lactation and their waste. Experiments were conducted in chambers at UC Davis that simulate freestall cow housing conditions. CH4 fluxes ranged from 125-374 lb/cow/year. The compounds with the highest fluxes from '3 cows+waste' treatments were: ammonia (1-18), methanol (0-2.3), acetone+propanal (0.2-0.7), dimethylsulfide (0-0.4), and mass 109 (likely ID = p-cresol; 0-0.3) in lb/cow/year. Mass 60 (likely ID = trimethylamine) and acetic acid were also abundant. There were 10s of additional compounds with detectable, but small, emissions. A few compounds that were likely emitted (i.e. ethanol, formaldehyde, and dimethylamine) were not quantified by the PTR-MS. The total flux for all measured organic gases (TOG = CH4 + PTR-MS VOCs(including acetone+propanal)) averaged 246±45 lb/cow/year for '3 cows+waste' treatments, and was dominated by methane (>98%). TOG flux for 'waste only' treatments averaged 1.1±0.1 lb/cow/year, and was instead dominated by VOC (>84%). The PTR-MS VOCs as a percent of TOG (0.6±0.2%) emitted from '3 cows+waste' treatments in chamber conditions was a factor of 10 smaller than that currently estimated by the California Air Resources Board. In addition, the ozone forming potentials of the most abundant VOCs are only about 10% those of typical combustion or plant

  10. On the long-term impact of emissions from central European cities on regional air quality

    NASA Astrophysics Data System (ADS)

    Huszar, P.; Belda, M.; Halenka, T.

    2016-02-01

    For the purpose of qualifying and quantifying the impact of urban emission from Central European cities on the present-day regional air quality, the regional climate model RegCM4.2 was coupled with the chemistry transport model CAMx, including two-way interactions. A series of simulations was carried out for the 2001-2010 period either with all urban emissions included (base case) or without considering urban emissions. Further, the sensitivity of ozone production to urban emissions was examined by performing reduction experiments with -20 % emission perturbation of NOx and/or non-methane volatile organic compounds (NMVOC). The modeling system's air quality related outputs were evaluated using AirBase, and EMEP surface measurements showed reasonable reproduction of the monthly variation for ozone (O3), but the annual cycle of nitrogen dioxide (NO2) and sulfur dioxide (SO2) is more biased. In terms of hourly correlations, values achieved for ozone and NO2 are 0.5-0.8 and 0.4-0.6, but SO2 is poorly or not correlated at all with measurements (r around 0.2-0.5). The modeled fine particulates (PM2.5) are usually underestimated, especially in winter, mainly due to underestimation of nitrates and carbonaceous aerosols. European air quality measures were chosen as metrics describing the cities emission impact on regional air pollution. Due to urban emissions, significant ozone titration occurs over cities while over rural areas remote from cities, ozone production is modeled, mainly in terms of number of exceedances and accumulated exceedances over the threshold of 40 ppbv. Urban NOx, SO2 and PM2.5 emissions also significantly contribute to concentrations in the cities themselves (up to 50-70 % for NOx and SO2, and up to 60 % for PM2.5), but the contribution is large over rural areas as well (10-20 %). Although air pollution over cities is largely determined by the local urban emissions, considerable (often a few tens of %) fraction of the concentration is attributable to

  11. Competing analysis of α and 2p2n-emission from compound nuclei formed in neutron induced reactions

    NASA Astrophysics Data System (ADS)

    Kaur, Amandeep; Sharma, Manoj K.

    2017-01-01

    The decay mechanism of compound system 61Ni* formed in fast neutron induced reactions is explored within the collective clusterization approach of the Dynamical Cluster-decay Model (DCM) in reference to a recent experiment over an energy spread of En = 1- 100 MeV. The excitation functions for the decay of the compound nucleus 61Ni* formed in the n +60Ni reaction show a double humped variation with incident beam energy where the peak at lower energy corresponds to α-emission while the one at higher energy originates from 2 p 2 n-emission. The experimentally observed transmutation of α-emission at lower energy into 2 p 2 n-emission at higher incident energies is explained on the basis of temperature dependence of the binding energies used within the framework of DCM. The cross-sections for the formation of the daughter nucleus 57Fe after emission of α-cluster from the 61Ni* nucleus are addressed by employing the neck length parameter (ΔR), finding decent agreement with the available experimental data. The calculations are done for non-sticking choice of moment of inertia (INS) in the centrifugal potential term, which forms the essential ingredient in DCM based calculations. In addition to this, the effect of mass (and charge) of the compound nucleus is exercised in view of α and 2 p 2 n emission and comparative study of the decay profiles of compound systems with mass A = 17-93 is employed to get better description of decay patterns.

  12. Aboveground and Belowground Herbivores Synergistically Induce Volatile Organic Sulfur Compound Emissions from Shoots but Not from Roots.

    PubMed

    Danner, Holger; Brown, Phil; Cator, Eric A; Harren, Frans J M; van Dam, Nicole M; Cristescu, Simona M

    2015-07-01

    Studies on aboveground (AG) plant organs have shown that volatile organic compound (VOC) emissions differ between simultaneous attack by herbivores and single herbivore attack. There is growing evidence that interactive effects of simultaneous herbivory also occur across the root-shoot interface. In our study, Brassica rapa roots were infested with root fly larvae (Delia radicum) and the shoots infested with Pieris brassicae, either singly or simultaneously, to study these root-shoot interactions. As an analytical platform, we used Proton Transfer Reaction Mass Spectrometry (PTR-MS) to investigate VOCs over a 3 day time period. Our set-up allowed us to monitor root and shoot emissions concurrently on the same plant. Focus was placed on the sulfur-containing compounds; methanethiol, dimethylsulfide (DMS), and dimethyldisulfide (DMDS), because these compounds previously have been shown to be biologically active in the interactions of Brassica plants, herbivores, parasitoids, and predators, yet have received relatively little attention. The shoots of plants simultaneously infested with AG and belowground (BG) herbivores emitted higher levels of sulfur-containing compounds than plants with a single herbivore species present. In contrast, the emission of sulfur VOCs from the plant roots increased as a consequence of root herbivory, independent of the presence of an AG herbivore. The onset of root emissions was more rapid after damage than the onset of shoot emissions. The shoots of double infested plants also emitted higher levels of methanol. Thus, interactive effects of root and shoot herbivores exhibit more strongly in the VOC emissions from the shoots than from the roots, implying the involvement of specific signaling interactions.

  13. [Emission characteristics and safety evaluation of volatile organic compounds in manufacturing processes of automotive coatings].

    PubMed

    Zeng, Pei-Yuan; Li, Jian-Jun; Liao, Dong-Qi; Tu, Xiang; Xu, Mei-Ying; Sun, Guo-Ping

    2013-12-01

    Emission characteristics of volatile organic compounds (VOCs) were investigated in an automotive coating manufacturing enterprise. Air samples were taken from eight different manufacturing areas in three workshops, and the species of VOCs and their concentrations were measured by gas chromatography-mass spectrometry (GC-MS). Safety evaluation was also conducted by comparing the concentration of VOCs with the permissible concentration-short term exposure limit (PC-STEL) regulated by the Ministry of Health. The results showed that fifteen VOCs were detected in the indoor air of the automotive coatings workshop, including benzene, toluene, ethylbenzene, xylene, ethyl acetate, butyl acetate, methyl isobutyl ketone, propylene glycol monomethyl ether acetate, trimethylbenzene and ethylene glycol monobutyl ether, Their concentrations widely ranged from 0.51 to 593.14 mg x m(-3). The concentrations of TVOCs were significantly different among different manufacturing processes. Even in the same manufacturing process, the concentrations of each component measured at different times were also greatly different. The predominant VOCs of indoor air in the workshop were identified to be ethylbenzene and butyl acetate. The concentrations of most VOCs exceeded the occupational exposure limits, so the corresponding control measures should be taken to protect the health of the workers.

  14. Impact of Marcellus Shale natural gas development in southwest Pennsylvania on volatile organic compound emissions and regional air quality.

    PubMed

    Swarthout, Robert F; Russo, Rachel S; Zhou, Yong; Miller, Brandon M; Mitchell, Brittney; Horsman, Emily; Lipsky, Eric; McCabe, David C; Baum, Ellen; Sive, Barkley C

    2015-03-03

    The Marcellus Shale is the largest natural gas deposit in the U.S. and rapid development of this resource has raised concerns about regional air pollution. A field campaign was conducted in the southwestern Pennsylvania region of the Marcellus Shale to investigate the impact of unconventional natural gas (UNG) production operations on regional air quality. Whole air samples were collected throughout an 8050 km(2) grid surrounding Pittsburgh and analyzed for methane, carbon dioxide, and C1-C10 volatile organic compounds (VOCs). Elevated mixing ratios of methane and C2-C8 alkanes were observed in areas with the highest density of UNG wells. Source apportionment was used to identify characteristic emission ratios for UNG sources, and results indicated that UNG emissions were responsible for the majority of mixing ratios of C2-C8 alkanes, but accounted for a small proportion of alkene and aromatic compounds. The VOC emissions from UNG operations accounted for 17 ± 19% of the regional kinetic hydroxyl radical reactivity of nonbiogenic VOCs suggesting that natural gas emissions may affect compliance with federal ozone standards. A first approximation of methane emissions from the study area of 10.0 ± 5.2 kg s(-1) provides a baseline for determining the efficacy of regulatory emission control efforts.

  15. Contribution of the gasoline distribution cycle to volatile organic compound emissions in the metropolitan area of Mexico City.

    PubMed

    Schifter, I; Magdaleno, M; Díaz, L; Krüger, B; León, J; Palmerín, M E; Casas, R; Melgarejo, A; López-Salinas, E

    2002-05-01

    Gasoline distribution in the metropolitan area of Mexico City (MAMC) represents an area of opportunity for the abatement of volatile organic compound (VOC) emissions. The gasoline distribution in this huge urban center encompasses several operations: (1) storage in bulk and distribution plants, (2) transportation to gasoline service stations, (3) unloading at service stations' underground tanks, and (4) gasoline dispensing. In this study, hydrocarbon (HC) emissions resulting from breathing losses in closed reservoirs, leakage, and spillage from the operations just listed were calculated using both field measurements and reported emission factors. The results show that the contribution of volatile HC emissions due to storage, distribution, and sales of gasoline is 6651 t/year, approximately 13 times higher than previously reported values. Tank truck transportation results in 53.9% of the gasoline emissions, and 31.5% of emissions are generated when loading the tank trucks. The high concentration of emissions in the gasoline transportation and loading operations by tank trucks has been ascribed to (1) highly frequent trips from distribution plant to gasoline stations, and vice versa, to cope with excessive gasoline sales per gasoline station; (2) low leakproofness of tank trucks; and (3) poor training of employees. In addition, the contribution to HC evaporative and exhaust emissions from the vehicles of the MAMC was also evaluated.

  16. Salt Lakes of Western Australia - Emissions of natural volatile organic compounds

    NASA Astrophysics Data System (ADS)

    Sattler, Tobias; Krause, Torsten; Schöler, Heinfried; Kamilli, Katharina; Held, Andreas; Zetzsch, Cornelius; Ofner, Johannes; Junkermann, Wolfgang; Atlas, Elliot

    2013-04-01

    Western Australia is a semi-/arid region that is heavily influenced by global climate change and agricultural land use. The area is known for its many saline lakes with a wide range of hydrogeochemical parameters. This area has been repeatedly investigated since 2006 and consists of ephemeral saline and saline groundwater sourced lakes with a pH reaching from 2.5 to 7.1. The semi-/arid region was originally covered by natural eucalyptus forests, but land-use has changed considerably after large scale deforestation from 1950 to 1970. Today the region is mostly used for growing wheat and live stock. The deforestation led to a rising groundwater table, bringing dissolved salts and minerals to the surface. In the last decades, a concurrent alteration of rain periods has been observed. A reason could be the regional formation of ultra-fine particles that were measured with car-based and airborne instruments around the salt lakes in several campaigns between 2006 and 2011. These ultra-fine particles emitted from the lakes and acting as cloud condensation nuclei can modify cloud microphysics and thus suppress rain events [1]. New data from a campaign in 2012 accentuates the importance of these hyper saline environments for the local climate. Ground-based particle measurements around the salt lakes in 2012 were accompanied by novel chamber experiments directly on the lakes. The 1.5 m³ cubic chamber was constructed from transparent PTFE foil permitting photochemistry within while preventing dilution of the air due to lateral wind transport. This experimental setup allows linking the measured data directly to the chemistry of and above the salt lakes. Another advantage of the PTFE chamber is the enrichment of volatile organic compounds (VOC) that are emitted from salt lakes as possible precursors for the ultra-fine particles. Chamber air was sampled using stainless steel canisters. Sediment, crust and water samples were taken for investigation of potential VOC emissions in

  17. Global biogenic volatile organic compound emissions in the ORCHIDEE and MEGAN models and sensitivity to key parameters

    NASA Astrophysics Data System (ADS)

    Messina, Palmira; Lathière, Juliette; Sindelarova, Katerina; Vuichard, Nicolas; Granier, Claire; Ghattas, Josefine; Cozic, Anne; Hauglustaine, Didier A.

    2016-11-01

    A new version of the biogenic volatile organic compounds (BVOCs) emission scheme has been developed in the global vegetation model ORCHIDEE (Organizing Carbon and Hydrology in Dynamic EcosystEm), which includes an extended list of biogenic emitted compounds, updated emission factors (EFs), a dependency on light for almost all compounds and a multi-layer radiation scheme. Over the 2000-2009 period, using this model, we estimate mean global emissions of 465 Tg C yr-1 for isoprene, 107.5 Tg C yr-1 for monoterpenes, 38 Tg C yr-1 for methanol, 25 Tg C yr-1 for acetone and 24 Tg C yr-1 for sesquiterpenes. The model results are compared to state-of-the-art emission budgets, showing that the ORCHIDEE emissions are within the range of published estimates. ORCHIDEE BVOC emissions are compared to the estimates of the Model of Emissions of Gases and Aerosols from Nature (MEGAN), which is largely used throughout the biogenic emissions and atmospheric chemistry community. Our results show that global emission budgets of the two models are, in general, in good agreement. ORCHIDEE emissions are 8 % higher for isoprene, 8 % lower for methanol, 17 % higher for acetone, 18 % higher for monoterpenes and 39 % higher for sesquiterpenes, compared to the MEGAN estimates. At the regional scale, the largest differences between ORCHIDEE and MEGAN are highlighted for isoprene in northern temperate regions, where ORCHIDEE emissions are higher by 21 Tg C yr-1, and for monoterpenes, where they are higher by 4.4 and 10.2 Tg C yr-1 in northern and southern tropical regions compared to MEGAN. The geographical differences between the two models are mainly associated with different EF and plant functional type (PFT) distributions, while differences in the seasonal cycle are mostly driven by differences in the leaf area index (LAI). Sensitivity tests are carried out for both models to explore the response to key variables or parameters such as LAI and light-dependent fraction (LDF). The ORCHIDEE and

  18. Highly efficient electroluminescence from a heterostructure device combined with emissive layered-perovskite and an electron-transporting organic compound

    NASA Astrophysics Data System (ADS)

    Hattori, Toshiaki; Taira, Takahiro; Era, Masanao; Tsutsui, Tetsuo; Saito, Shugu

    1996-05-01

    Two Pbl-based layer perovskite compounds, which possess cyclohexenylethylamine or phenylbutylamine as an organic ammonium layer, were newly found to exhibit efficient exciton emission due to their self-organized quantum well structure where a lead halide semiconducting layer and an organic ammonium dielectric layer are alternately piled up. We prepared heterostructure electroluminescent devices using the combination of the emissive layered perovskite and an electron-transporting oxadiazole. When the heterostructure devices were driven at 110 K, greenish emission, which corresponded well to the exciton emission, was observed. In the device using the perovskite with an organic layer of cyclohexenythylamine, a high luminance exceeding 4000 cd m -2 and high external EL quantum efficiency of 2.8% were attained at a current density of 50 mA cm -2 at an applied voltage of 24 V.

  19. Climate change-induced vegetation change as a driver of increased subarctic biogenic volatile organic compound emissions

    PubMed Central

    Valolahti, Hanna; Kivimäenpää, Minna; Faubert, Patrick; Michelsen, Anders; Rinnan, Riikka

    2015-01-01

    Emissions of biogenic volatile organic compounds (BVOCs) have been earlier shown to be highly temperature sensitive in subarctic ecosystems. As these ecosystems experience rapidly advancing pronounced climate warming, we aimed to investigate how warming affects the BVOC emissions in the long term (up to 13 treatment years). We also aimed to assess whether the increased litterfall resulting from the vegetation changes in the warming subarctic would affect the emissions. The study was conducted in a field experiment with factorial open-top chamber warming and annual litter addition treatments on subarctic heath in Abisko, northern Sweden. After 11 and 13 treatment years, BVOCs were sampled from plant communities in the experimental plots using a push–pull enclosure technique and collection into adsorbent cartridges during the growing season and analyzed with gas chromatography–mass spectrometry. Plant species coverage in the plots was analyzed by the point intercept method. Warming by 2 °C caused a 2-fold increase in monoterpene and 5-fold increase in sesquiterpene emissions, averaged over all measurements. When the momentary effect of temperature was diminished by standardization of emissions to a fixed temperature, warming still had a significant effect suggesting that emissions were also indirectly increased. This indirect increase appeared to result from increased plant coverage and changes in vegetation composition. The litter addition treatment also caused significant increases in the emission rates of some BVOC groups, especially when combined with warming. The combined treatment had both the largest vegetation changes and the highest BVOC emissions. The increased emissions under litter addition were probably a result of a changed vegetation composition due to alleviated nutrient limitation and stimulated microbial production of BVOCs. We suggest that the changes in the subarctic vegetation composition induced by climate warming will be the major factor

  20. Climate change-induced vegetation change as a driver of increased subarctic biogenic volatile organic compound emissions.

    PubMed

    Valolahti, Hanna; Kivimäenpää, Minna; Faubert, Patrick; Michelsen, Anders; Rinnan, Riikka

    2015-09-01

    Emissions of biogenic volatile organic compounds (BVOCs) have been earlier shown to be highly temperature sensitive in subarctic ecosystems. As these ecosystems experience rapidly advancing pronounced climate warming, we aimed to investigate how warming affects the BVOC emissions in the long term (up to 13 treatment years). We also aimed to assess whether the increased litterfall resulting from the vegetation changes in the warming subarctic would affect the emissions. The study was conducted in a field experiment with factorial open-top chamber warming and annual litter addition treatments on subarctic heath in Abisko, northern Sweden. After 11 and 13 treatment years, BVOCs were sampled from plant communities in the experimental plots using a push-pull enclosure technique and collection into adsorbent cartridges during the growing season and analyzed with gas chromatography-mass spectrometry. Plant species coverage in the plots was analyzed by the point intercept method. Warming by 2 °C caused a 2-fold increase in monoterpene and 5-fold increase in sesquiterpene emissions, averaged over all measurements. When the momentary effect of temperature was diminished by standardization of emissions to a fixed temperature, warming still had a significant effect suggesting that emissions were also indirectly increased. This indirect increase appeared to result from increased plant coverage and changes in vegetation composition. The litter addition treatment also caused significant increases in the emission rates of some BVOC groups, especially when combined with warming. The combined treatment had both the largest vegetation changes and the highest BVOC emissions. The increased emissions under litter addition were probably a result of a changed vegetation composition due to alleviated nutrient limitation and stimulated microbial production of BVOCs. We suggest that the changes in the subarctic vegetation composition induced by climate warming will be the major factor

  1. Emission characteristics of volatile organic compounds from coal-, coal gangue-, and biomass-fired power plants in China

    NASA Astrophysics Data System (ADS)

    Yan, Yulong; Yang, Chao; Peng, Lin; Li, Rumei; Bai, Huiling

    2016-10-01

    Face the large electricity demand, thermal power generation still derives the main way of electricity supply in China, account for 78.19% of total electricity production in 2013. Three types of thermal power plants, including coal-fired power plant, coal gangue-fired power plant and biomass-fired power plant, were chosen to survey the source profile, chemical reactivity and emission factor of VOCs during the thermal power generation. The most abundant compounds generated during coal- and coal gangue-fired power generation were 1-Butene, Styrene, n-Hexane and Ethylene, while biomass-fired power generation were Propene, 1-Butenen, Ethyne and Ethylene. The ratios of B/T during thermal power generation in this study was 0.8-2.6, which could be consider as the characteristics of coal and biomass burning. The field tested VOCs emission factor from coal-, coal gangue- and biomass-fired power plant was determined to be 0.88, 0.38 and 3.49 g/GJ, or showed as 0.023, 0.005 and 0.057 g/kg, with the amount of VOCs emission was 44.07, 0.08, 0.45 Gg in 2013, respectively. The statistical results of previous emission inventory, which calculated the VOCs emission used previous emission factor, may overestimate the emission amount of VOCs from thermal power generation in China.

  2. Particulate metals and organic compounds from electronic and tobacco-containing cigarettes: comparison of emission rates and secondhand exposure.

    PubMed

    Saffari, Arian; Daher, Nancy; Ruprecht, Ario; De Marco, Cinzia; Pozzi, Paolo; Boffi, Roberto; Hamad, Samera H; Shafer, Martin M; Schauer, James J; Westerdahl, Dane; Sioutas, Constantinos

    2014-01-01

    In recent years, electronic cigarettes have gained increasing popularity as alternatives to normal (tobacco-containing) cigarettes. In the present study, particles generated by e-cigarettes and normal cigarettes have been analyzed and the degree of exposure to different chemical agents and their emission rates were quantified. Despite the 10-fold decrease in the total exposure to particulate elements in e-cigarettes compared to normal cigarettes, specific metals (e.g. Ni and Ag) still displayed a higher emission rate from e-cigarettes. Further analysis indicated that the contribution of e-liquid to the emission of these metals is rather minimal, implying that they likely originate from other components of the e-cigarette device or other indoor sources. Organic species had lower emission rates during e-cigarette consumption compared to normal cigarettes. Of particular note was the non-detectable emission of polycyclic aromatic hydrocarbons (PAHs) from e-cigarettes, while substantial emission of these species was observed from normal cigarettes. Overall, with the exception of Ni, Zn, and Ag, the consumption of e-cigarettes resulted in a remarkable decrease in secondhand exposure to all metals and organic compounds. Implementing quality control protocols on the manufacture of e-cigarettes would further minimize the emission of metals from these devices and improve their safety and associated health effects.

  3. Emission characteristics of nitrogen- and sulfur-containing odorous compounds during different sewage sludge chemical conditioning processes.

    PubMed

    Liu, Huan; Luo, Guang-Qian; Hu, Hong-Yun; Zhang, Qiang; Yang, Jia-Kuan; Yao, Hong

    2012-10-15

    Chemical conditioners are often used to enhance sewage sludge dewaterability through altering sludge properties and flocs structure, both affect odorous compounds emissions not only during sludge conditioning but also in subsequent sludge disposal. This study was to investigate emission characteristics of ammonia (NH(3)), sulfur dioxide (SO(2)), hydrogen sulfide (H(2)S) and carbonyl sulfide (COS) generated from sewage sludge conditioned by three representative conditioners, i.e., organic polymers, iron salts and skeleton builders, F-S (Fenton's reagent and skeleton builders) composite conditioner. The results demonstrate that polyacrylamide (PAM) has an insignificant effect on emission characteristics of nitrogen- and sulfur-containing odorous compounds, because the properties, sulfur and nitrogen speciations are similar in PAM-conditioned sludge and raw sludge (RS). Significant increases of SO(2) and H(2)S emissions in the H(2)SO(4) conditioning process were observed due to the accelerated decomposition of sulfur-containing amino acids in acidic environment. Fenton peroxidation facilitates the formation of COS. CaO can reduce sulfur-containing gases emission via generation of calcium sulfate. However, under strong alkaline conditions, free ammonia or protonated amine in sludge can be easily converted to volatile ammonia, resulting in a significant release of NH(3).

  4. Quantifying the air pollutants emission reduction during the 2008 Olympic games in Beijing.

    PubMed

    Wang, Shuxiao; Zhao, Meng; Xing, Jia; Wu, Ye; Zhou, Yu; Lei, Yu; He, Kebin; Fu, Lixin; Hao, Jiming

    2010-04-01

    Air quality was a vital concern for the Beijing Olympic Games in 2008. To strictly control air pollutant emissions and ensure good air quality for the Games, Beijing municipal government announced an "Air Quality Guarantee Plan for the 29th Olympics in Beijing". In order to evaluate the effectiveness of the guarantee plan, this study analyzed the air pollutant emission reductions during the 29th Olympiad in Beijing. In June 2008, daily emissions of SO(2), NO(X), PM(10), and NMVOC in Beijing were 103.9 t, 428.5 t, 362.7 t, and 890.0 t, respectively. During the Olympic Games, the daily emissions of SO(2), NO(X), PM(10), and NMVOC in Beijing were reduced to 61.6 t, 229.1 t, 164.3 t, and 381.8 t -41%, 47%, 55%, and 57% lower than June 2008 emission levels. Closing facilities producing construction materials reduced the sector's SO(2) emissions by 85%. Emission control measures for mobile sources, including high-emitting vehicle restrictions, government vehicle use controls, and alternate day driving rules for Beijing's 3.3 million private cars, reduced mobile source NO(X) and NMVOC by 46% and 57%, respectively. Prohibitions on building construction reduced the sector's PM(10) emissions by approximately 90% or total PM(10) by 35%. NMVOC reductions came mainly from mobile source and fugitive emission reductions. Based on the emission inventories developed in this study, the CMAQ model was used to simulate Beijing's ambient air quality during the Olympic Games. The model results accurately reflect the environmental monitoring data providing evidence that the emission inventories in this study are reasonably accurate and quantitatively reflect the emission changes attributable to air pollution control measures taken during the 29th Olympic Games in 2008.

  5. Current emission trends for nitrogen oxides, sulfur dioxide, and volatile organic compounds by month and state: Methodology and results

    SciTech Connect

    Kohout, E.J.; Miller, D.J.; Nieves, L.A.; Rothman, D.S.; Saricks, C.L.; Stodolsky, F.; Hanson, D.A.

    1990-08-01

    This report presents estimates of monthly sulfur dioxide (SO{sub 2}), nitrogen oxides (NO{sub x}), and nonmethane voltatile organic compound (VOC) emissions by sector, region, and state in the contiguous United States for the years 1975 through 1988. This work has been funded as part of the National Acid Precipitation Assessment Program's Emissions and Controls Task Group by the US Department of Energy (DOE) Office of Fossil Energy (FE). The DOE project officer is Edward C. Trexler, DOE/FE Office of Planning and Environment.

  6. Current emission trends for nitrogen oxides, sulfur dioxide, and volatile organic compounds by month and state: Methodology and results

    SciTech Connect

    Kohout, E.J.; Miller, D.J.; Nieves, L.A.; Rothman, D.S.; Saricks, C.L.; Stodolsky, F.; Hanson, D.A.

    1990-08-01

    This report presents estimates of monthly sulfur dioxide (SO{sub 2}), nitrogen oxides (NO{sub x}), and nonmethane voltatile organic compound (VOC) emissions by sector, region, and state in the contiguous United States for the years 1975 through 1988. This work has been funded as part of the National Acid Precipitation Assessment Program`s Emissions and Controls Task Group by the US Department of Energy (DOE) Office of Fossil Energy (FE). The DOE project officer is Edward C. Trexler, DOE/FE Office of Planning and Environment.

  7. Biogenic volatile organic compounds (BVOCs) emission of Scots pine under drought stress - a 13CO2 labeling study to determine de novo and pool emissions under different treatments

    NASA Astrophysics Data System (ADS)

    Lüpke, M.

    2015-12-01

    Plants emit biogenic volatile organic compounds (BVOCs) to e.g. communicate and to defend herbivores. Yet BVOCs also impact atmospheric chemistry processes, and lead to e.g. the built up of secondary organic aerosols. Abiotic stresses, such as drought, however highly influence plant physiology and subsequently BVOCs emission rates. In this study, we investigated the effect of drought stress on BVOCs emission rates of Scots pine trees, a de novo and pool emitter, under controlled climate chamber conditions within a dynamic enclosure system consisting of four plant chambers. Isotopic labeling with 13CO2 was used to detect which ratio of emissions of BVOCs derives from actual synthesis and from storage organs under different treatments. Additionally, the synthesis rate of the BVOCs synthesis can be determined. The experiment consisted of two campaigns (July 2015 and August 2015) of two control and two treated trees respectively in four controlled dynamic chambers simultaneously. Each campaign lasted for around 21 days and can be split into five phases: adaptation, control, dry-out, drought- and re-watering phase. The actual drought phase lasted around five days. During the campaigns two samples of BVOCs emissions were sampled per day and night on thermal desorption tubes and analyzed by a gas chromatograph coupled with a mass spectrometer and a flame ionization detector. Additionally, gas exchange of water and CO2, soil moisture, as well as leaf and chamber temperature was monitored continuously. 13CO2 labeling was performed simultaneously in all chambers during the phases control, drought and re-watering for five hours respectively. During the 13CO2 labeling four BVOCs emission samples per chamber were taken to identify the labeling rate on emitted BVOCs. First results show a decrease of BVOCs emissions during the drought phase and a recovery of emission after re-watering, as well as different strength of reduction of single compounds. The degree of labeling with 13

  8. Top-Down Constraints on the Emissions of Anthropogenic Volatile Organic Compounds from a Mega-City

    NASA Astrophysics Data System (ADS)

    De Gouw, J. A.; Warneke, C.; Borbon, A.; Gilman, J. B.; Kuster, W. C.; Parrish, D. D.; Atlas, E. L.; Blake, D. R.

    2012-12-01

    During the CalNex study in May-June of 2010, an extensive set of volatile organic compounds (VOCs) was measured in the Los Angeles basin and its in- and outflow areas. Measurements were made from the NOAA WP-3D research aircraft, the research vessel Atlantis and a ground site in Pasadena, California. In this presentation, the results are used to derive top-down constraints on the emissions of anthropogenic VOCs from this North-American megacity. The VOC data from CalNex in 2010 are put in perspective by comparing them with results from an earlier flight of the NOAA WP-3D in the Los Angeles basin in 2002, from a number of other earlier studies and from two different air quality monitoring networks. Strongly decreasing trends of ~7% per year are observed for most VOCs that are emitted from motor vehicles or photo-chemically produced from these emissions. Decreasing trends are less strong for small alkanes, which are mostly from natural gas related emissions, and oxygenated VOCs produced from them. The composition of urban VOC emissions was determined using the data obtained by gas-chromatography mass spectrometry at the ground site in Pasadena. Emission ratios of hydrocarbons versus ethyne were obtained using two methods. First, emission ratios were determined from nighttime data only. Second, the degree of photochemical processing of the sampled air masses was estimated, and emission ratios were determined by extrapolating to a zero photochemical age. Both methods agreed within the combined uncertainties for most VOCs. The composition of urban VOC emissions in Los Angeles was compared with other urban regions including in the U.S. and Europe and found to be similar. Measurements of ethanol at the ground site in Pasadena showed much higher mixing ratios than observed earlier in the northeastern U.S. The difference is attributed in part to the strongly increased use of fuel ethanol in the U.S.: in 2010, about 10% of gasoline consisted of ethanol, whereas that

  9. 75 FR 82363 - Approval and Promulgation of Implementation Plans; Ohio; Volatile Organic Compound Emission...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-30

    ... AGENCY 40 CFR Part 52 Approval and Promulgation of Implementation Plans; Ohio; Volatile Organic Compound... printing volatile organic compound (VOC) rule for approval into the Ohio State Implementation Plan (SIP..., Volatile organic compounds. Dated: December 17, 2010. Bharat Mathur, Acting Regional Administrator,...

  10. Relative impact of on-road vehicular and point-source industrial emissions of air pollutants in a medium-sized Andean city

    NASA Astrophysics Data System (ADS)

    González, C. M.; Gómez, C. D.; Rojas, N. Y.; Acevedo, H.; Aristizábal, B. H.

    2017-03-01

    Cities in emerging countries are facing a fast growth and urbanization; however, the study of air pollutant emissions and its dynamics is scarce, making their populations vulnerable to potential effects of air pollution. This situation is critical in medium-sized urban areas built along the tropical Andean mountains. This work assesses the contribution of on-road vehicular and point-source industrial activities in the medium-sized Andean city of Manizales, Colombia. Annual fluxes of criteria pollutants, NMVOC, and greenhouse gases were estimated. Emissions were dominated by vehicular activity, with more than 90% of total estimated releases for the majority of air pollutants. On-road vehicular emissions for CO (43.4 Gg/yr) and NMVOC (9.6 Gg/yr) were mainly associated with the use of motorcycles (50% and 81% of total CO and NMVOC emissions respectively). Public transit buses were the main source of PM10 (47%) and NOx (48%). The per-capita emission index was significantly higher in Manizales than in other medium-sized cities, especially for NMVOC, CO, NOx and CO2. The unique mountainous terrain of Andean cities suggest that a methodology based on VSP model could give more realistic emission estimates, with additional model components that include slope and acceleration. Food and beverage facilities were the main contributors of point-source industrial emissions for PM10 (63%), SOx (55%) and NOx (45%), whereas scrap metal recycling had high emissions of CO (73%) and NMVOC (47%). Results provide the baseline for ongoing research in atmospheric modeling and urban air quality, in order to improve the understanding of air pollutant fluxes, transport and transformation in the atmosphere. In addition, this emission inventory could be used as a tool to identify areas of public health exposure and provide information for future decision makers.

  11. Headspace solid-phase microextraction--comprehensive two-dimensional gas chromatography of wound induced plant volatile organic compound emissions.

    PubMed

    Perera, Ranjini M M; Marriott, Philip J; Galbally, Ian E

    2002-12-01

    Plant emissions of volatile organic compounds from mechanically wounded Agrostis stolonifera, Pennisetum clandestinum, Eucalyptus leucoxylon and Trifolium repens have been sampled by headspace-solid phase microextraction (HS-SPME) and analysed by using comprehensive two-dimensional gas chromatography (GCxGC) for measurement of the plant emissions. GCxGC produces a fingerprint of the volatile organic compounds in a 2D separation space that may be approximately interpreted as a boiling point-polarity space, and may then be presented as a two-dimensional contour plot. This allows identification of sample-dependent variations in component distributions in the 2D plot, which will contain information about plant differences and should therefore facilitate recognition of different plant materials and displays the gross differences in volatiles between each plant species.

  12. Biogenic Volatile Organic Compound (BVOC) emissions from agricultural crop species: is guttation a possible source for methanol emissions following light/dark transition ?

    NASA Astrophysics Data System (ADS)

    Mozaffar, Ahsan; Amelynck, Crist; Bachy, Aurélie; Digrado, Anthony; Delaplace, Pierre; du Jardin, Patrick; Fauconnier, Marie-Laure; Schoon, Niels; Aubinet, Marc; Heinesch, Bernard

    2015-04-01

    In the framework of the CROSTVOC (CROp STress VOC) project, the exchange of biogenic volatile organic compounds (BVOCs) between two important agricultural crop species, maize and winter wheat, and the atmosphere has recently been measured during an entire growing season by using the eddy covariance technique. Because of the co-variation of BVOC emission drivers in field conditions, laboratory studies were initiated in an environmental chamber in order to disentangle the responses of the emissions to variations of the individual environmental parameters (such as PPFD and temperature) and to diverse abiotic stress factors. Young plants were enclosed in transparent all-Teflon dynamic enclosures (cuvettes) through which BVOC-free and RH-controlled air was sent. BVOC enriched air was subsequently sampled from the plant cuvettes and an empty cuvette (background) and analyzed for BVOCs in a high sensitivity Proton Transfer Reaction Mass Spectrometer (hs-PTR-MS) and for CO2 in a LI-7000 non-dispersive IR gas analyzer. Emissions were monitored at constant temperature (25 °C) and at a stepwise varying PPFD pattern (0-650 µmol m-2 s-1). For maize plants, sudden light/dark transitions at the end of the photoperiod were accompanied by prompt and considerable increases in methanol (m/z 33) and water vapor (m/z 39) emissions. Moreover, guttation droplets appeared on the sides and the tips of the leaves within a few minutes after light/dark transition. Therefore the assumption has been raised that methanol is also coming out with guttation fluid from the leaves. Consequently, guttation fluid was collected from young maize and wheat plants, injected in an empty enclosure and sampled by PTR-MS. Methanol and a large number of other compounds were observed from guttation fluid. Recent studies have shown that guttation from agricultural crops frequently occurs in field conditions. Further research is required to find out the source strength of methanol emissions by this guttation

  13. Compound

    NASA Astrophysics Data System (ADS)

    Suzumura, Akitoshi; Watanabe, Masaki; Nagasako, Naoyuki; Asahi, Ryoji

    2014-06-01

    Recently, Cu-based chalcogenides such as Cu3SbSe4, Cu2Se, and Cu2SnSe3 have attracted much attention because of their high thermoelectric performance and their common feature of very low thermal conductivity. However, for practical use, materials without toxic elements such as selenium are preferable. In this paper, we report Se-free Cu3SbS4 thermoelectric material and improvement of its figure of merit ( ZT) by chemical substitutions. Substitutions of 3 at.% Ag for Cu and 2 at.% Ge for Sb lead to significant reductions in the thermal conductivity by 37% and 22%, respectively. These substitutions do not sacrifice the power factor, thus resulting in enhancement of the ZT value. The sensitivity of the thermal conductivity to chemical substitutions in these compounds is discussed in terms of the calculated phonon dispersion and previously proposed models for Cu-based chalcogenides. To improve the power factor, we optimize the hole carrier concentration by substitution of Ge for Sb, achieving a power factor of 16 μW/cm K2 at 573 K, which is better than the best reported for Se-based Cu3SbSe4 compounds.

  14. Air-surface exchange of nonmethane organic compounds at a Grassland site: seasonal variations and stressed emissions.

    SciTech Connect

    Fukui, Y.; Doskey, P. V.; Environmental Research

    1998-06-20

    Emissions of nonmethane organic compounds (NMOCs) were measured by a static enclosure technique at a grassland site in the Midwestern United States during the growing seasons over a 2-year period. A mixture of nonmethane hydrocarbons (NMHCs) and oxygenated hydrocarbons (OxHCs) was emitted from the surface at rates exhibiting large seasonal and year-to-year variations. The average emission rate (and standard error) of the total NMOCs around noontime on sunny days during the growing seasons for the 2-year period was 1,300 {+-} 170 {micro}g m-2 h-1 (mass of the total NMOCs per area of enclosed soil surface per hour) or 5.5 {+-} 0.9 {micro}g g-1 h-1 (mass of the total NMOCs per mass of dry plant biomass in an enclosure per hour), with about 10% and 70% of the emissions being composed of tentatively identified NMHCs and OxHCs, respectively. Methanol was apparently derived from both the soil and vegetation and exhibited an average emission rate of 460 {+-} 73 {micro}g m-2 h-1 (1.4 {+-} 0.2 {micro}g g-1 h-1), which was the largest emission among the NMOCs. The year-to-year variation in the precipitation pattern greatly affected the NMOC emission rates. Emission rates normalized to biomass density exhibited a linear decrease as the growing season progressed. The emission rates of some NMOCs, particularly the OxHCs, from vegetation subjected to hypoxia, frost, and physical stresses were significantly greater than the average values observed at the site. Emissions of monoterpenes (a- and {beta}-pinene, limonene, and myrcene) and cis-3-hexen-1-ol were accelerated during the flowering of the plants and were much greater than those predicted by algorithms that correlated emission rates with temperature. Herbaceous vegetation is estimated to contribute about 40% and 50% of the total NMOC and monoterpene emissions, respectively, in grasslands; the remaining contributions are from woody species within grasslands. Contributions of isoprene emissions from herbaceous vegetation in

  15. Air-surface exchange of nonmethane organic compounds at a grassland site: Seasonal variations and stressed emissions

    NASA Astrophysics Data System (ADS)

    Fukui, Yoshiko; Doskey, Paul V.

    1998-06-01

    Emissions of nonmethane organic compounds (NMOCs) were measured by a static enclosure technique at a grassland site in the midwestern United States during the growing seasons over a 2-year period. A mixture of nonmethane hydrocarbons (NMHCs) and oxygenated hydrocarbons (OxHCs) was emitted from the surface at rates exhibiting large seasonal and year-to-year variations. The average emission rate (and standard error) of the total NMOCs around noontime on sunny days during the growing seasons for the 2-year period was 1,300±170 μg m-2 h-1 (mass of the total NMOCs per area of enclosed soil surface per hour) or 5.5±0.9 μg g-1 h-1 (mass of the total NMOCs per mass of dry plant biomass in an enclosure per hour), with about 10% and 70% of the emissions being composed of tentatively identified NMHCs and OxHCs, respectively. Methanol was apparently derived from both the soil and vegetation and exhibited an average emission rate of 460±73 μg m-2 h-1 (1.4±0.2 μg g-1 h-1), which was the largest emission among the NMOCs. The year-to-year variation in the precipitation pattern greatly affected the NMOC emission rates. Emission rates normalized to biomass density exhibited a linear decrease as the growing season progressed. The emission rates of some NMOCs, particularly the OxHCs, from vegetation subjected to hypoxia, frost, and physical stresses were significantly greater than the average values observed at the site. Emissions of monoterpenes (α- and β-pinene, limonene, and myrcene) and cis-3-hexen-l-ol were accelerated during the flowering of the plants and were much greater than those predicted by algorithms that correlated emission rates with temperature. Herbaceous vegetation is estimated to contribute about 40% and 50% of the total NMOC and monoterpene emissions, respectively, in grasslands; the remaining contributions are from woody species within grasslands. Contributions of isoprene emissions from herbaceous vegetation in grasslands are negligible. Grasslands are

  16. Influence of aeration on volatile sulfur compounds (VSCs) and NH3 emissions during aerobic composting of kitchen waste.

    PubMed

    Zhang, Hongyu; Li, Guoxue; Gu, Jun; Wang, Guiqin; Li, Yangyang; Zhang, Difang

    2016-12-01

    This study investigates the influence of aeration on volatile sulfur compounds (VSCs) and ammonia (NH3) emissions during kitchen waste composting. Aerobic composting of kitchen waste and cornstalks was conducted at a ratio of 85:15 (wet weight basis) in 60L reactors for 30days. The gas emissions were analyzed with force aeration at rates of 0.1 (A1), 0.2 (A2) and 0.3 (A3) L (kgDMmin)(-1), respectively. Results showed that VSCs emission at the low aeration rate (A1) was more significant than that at other two rates (i.e., A2 and A3 treatment), where no considerable emission difference was observed. On the other hand, NH3 emission reduced as the aeration rate decreased. It is noteworthy that the aeration rate did not significantly affect the compost quality. These results suggest that the aeration rate of 0.2L (kgDMmin)(-1) may be applied to control VSCs and NH3 emissions during kitchen waste composting.

  17. Effect of land-use change and management on biogenic volatile organic compound emissions--selecting climate-smart cultivars.

    PubMed

    Rosenkranz, Maaria; Pugh, Thomas A M; Schnitzler, Jörg-Peter; Arneth, Almut

    2015-09-01

    Land-use change (LUC) has fundamentally altered the form and function of the terrestrial biosphere. Increasing human population, the drive for higher living standards and the potential challenges of mitigating and adapting to global environmental change mean that further changes in LUC are unavoidable. LUC has direct consequences on climate not only via emissions of greenhouse gases and changing the surface energy balance but also by affecting the emission of biogenic volatile organic compounds (BVOCs). Isoprenoids, which dominate global BVOC emissions, are highly reactive and strongly modify atmospheric composition. The effects of LUC on BVOC emissions and related atmospheric chemistry have been largely ignored so far. However, compared with natural ecosystems, most tree species used in bioenergy plantations are strong BVOC emitters, whereas intensively cultivated crops typically emit less BVOCs. Here, we summarize the current knowledge on LUC-driven BVOC emissions and how these might affect atmospheric composition and climate. We further discuss land management and plant-breeding strategies, which could be taken to move towards climate-friendly BVOC emissions while simultaneously maintaining or improving key ecosystem functions such as crop yield under a changing environment.

  18. [Volatile organic compounds (VOCs) emitted from wood furniture--estimation of emission rate by passive flux sampler].

    PubMed

    Jinno, Hideto; Tanaka-Kagawa, Toshiko; Furuta, Mitsuko; Shibatsuji, Masayoshi; Nishimura, Tetsuji

    2011-01-01

    The aim of this study was to evaluate aldehydes and other volatile organic compounds (VOCs) emission from furniture, which may cause hazardous influence on human being such as sick building/sick house syndrome. In this study, VOCs emitted from six kinds of wood furniture, including three set of dining tables and three beds, were analyzed by large chamber test method (JIS A 1911). Based on the emission rates of total VOCs (TVOC), the impacts on the indoor TVOC was estimated by the simulation model with volume of 20 m3 and ventilation frequency of 0.5 times/h. The estimated increment of formaldehyde were exceeded the guideline value (100 microg/m3) in one set of dining table and one bed. The estimated TVOC increment values were exceeded the provisional target value for indoor air (400 microg/m3) in two sets of dining tables and two beds. These results revealed that VOC emissions from wood furniture may influence significantly indoor air quality. Also, in this study, to establish the alternative method for large chamber test methods, emission rates from representative five areas of furniture unit were evaluated by passive sampling method using flux sampler and emission rate from full-sized furniture was predicted. Emission rates predicted by flux passive sampler were 10-106% (formaldehyde) and 8-141% (TVOC) of the data measured using large chamber test, respectively.

  19. Thermal desorption-gas chromatography for the determination of emission of volatile organic compounds from furnishing materials.

    PubMed

    Igielska, B; Wiglusz, R; Jarnuszkiewicz, I

    1995-01-01

    In order to determine volatile organic compounds (VOC) released from the building and furnishing materials gas chromatography with air samples enrichment on Tenax TA and thermal desorption was used. The results obtained were compared with the results of air samples enrichment on active carbon with carbon disulfide extraction. To the thermal desorption the home made device, a similar to device developed at Research Triangle Institute (USA), was used. The both methods of the air samples enrichment with thermal desorption or carbon disulfide extraction showed that the emission of the volatile organic compounds from the PVC floor covering is very low within the range from 0.01 to 0.03 mg/m2.h. Thermal desorption technique allows to detect a larger number of compounds in trace levels.

  20. Emissions of volatile organic compounds and leaf structural characteristics of European aspen (Populus tremula) grown under elevated ozone and temperature.

    PubMed

    Hartikainen, Kaisa; Nerg, Anne-Marja; Kivimäenpää, Minna; Kontunen-Soppela, Sari; Mäenpää, Maarit; Oksanen, Elina; Rousi, Matti; Holopainen, Toini

    2009-09-01

    Northern forest trees are challenged to adapt to changing climate, including global warming and increasing tropospheric ozone (O(3)) concentrations. Both elevated O(3) and temperature can cause significant changes in volatile organic compound (VOC) emissions as well as in leaf anatomy that can be related to adaptation or increased stress tolerance, or are signs of damage. Impacts of moderately elevated O(3) (1.3x ambient) and temperature (ambient + 1 degrees C), alone and in combination, on VOC emissions and leaf structure of two genotypes (2.2 and 5.2) of European aspen (Populus tremula L.) were studied in an open-field experiment in summer 2007. The impact of O(3) on measured variables was minor, but elevated temperature significantly increased emissions of total monoterpenes and green leaf volatiles. Genotypic differences in the responses to warming treatment were also observed. alpha-Pinene emission, which has been suggested to protect plants from elevated temperature, increased from genotype 5.2 only. Isoprene emission from genotype 2.2 decreased, whereas genotype 5.2 was able to retain high isoprene emission level also under elevated temperature. Elevated temperature also caused formation of thinner leaves, which was related to thinning of epidermis, palisade and spongy layers as well as reduced area of palisade cells. We consider aspen genotype 5.2 to have better potential for adaptation to increasing temperature because of thicker photosynthetic active palisade layer and higher isoprene and alpha-pinene emission levels compared to genotype 2.2. Our results show that even a moderate elevation in temperature is efficient enough to cause notable changes in VOC emissions and leaf structure of these aspen genotypes, possibly indicating the effort of the saplings to adapt to changing climate.

  1. Optimizing the emission inventory of volatile organic compounds (VOCs) based on network observations

    NASA Astrophysics Data System (ADS)

    Chen, Sheng-Po; Liu, Wen-Tzu; Ou-Yang, Chang-Feng; Chang, Julius S.; Wang, Jia-Lin

    2014-02-01

    Hourly observations of 56 non-methane hydrocarbons (NMHCs) performed by a network of photochemical assessment monitoring stations (PAMS) at 11 locations across Taiwan were used to evaluate 56 speciated emissions and the resulting simulations of an air quality model. Based on the PAMS observations at two urban sites, emission modification was made for the 56 PAMS species in the model. To further test the applicability of this emission correction approach, the same modified emissions were subject to seven different meteorological conditions and comparison with observations of all the 11 PAMS sites. Originally there was a minimum of only 8 of 56 species showed agreement with observations for the worst of the 11 PAMS sites and 28 of 56 species for the best site. With modified emissions, the number increased to 13-52 species across the 11 PAMS sites, demonstrating that the simple urban based correction procedure has broad applicability. When applying this modification of PAMS emissions to the simulations of other air quality gases, SO2 and NOx showed small changes compared with observations (-0.27% and -2.51%, respectively), while total VOC concentrations showed significant changes (+15.28%) as a result of the adjustment in VOC emissions (+26.7%). Although VOCs are the precursor of ozone, the relatively large changes in VOC did not seem to affect ozone formation to the similar extent, only resulting in the changes of average O3 by 2.9 ppb (+9.41%). It shows that although the emission modification improves individual VOC simulations, the performance in oxidant simulation is still largely unaltered. Although the original U.S. VOC emission profiles can capture the general features of ambient VOCs, further optimization of emissions may still be needed by referencing extensive observations, so that emissions can better fit domestic conditions and accuracy in model simulations can be improved.

  2. Estimating emissions from crop residue open burning in China based on statistics and MODIS fire products.

    PubMed

    Li, Jing; Bo, Yu; Xie, Shaodong

    2016-06-01

    With the objective of reducing the large uncertainties in the estimations of emissions from crop residue open burning, an improved method for establishing emission inventories of crop residue open burning at a high spatial resolution of 0.25°×0.25° and a temporal resolution of 1month was established based on the moderate resolution imaging spectroradiometer (MODIS) Thermal Anomalies/Fire Daily Level3 Global Product (MOD/MYD14A1). Agriculture mechanization ratios and regional crop-specific grain-to-straw ratios were introduced to improve the accuracy of related activity data. Locally observed emission factors were used to calculate the primary pollutant emissions. MODIS satellite data were modified by combining them with county-level agricultural statistical data, which reduced the influence of missing fire counts caused by their small size and cloud cover. The annual emissions of CO2, CO, CH4, nonmethane volatile organic compounds (NMVOCs), N2O, NOx, NH3, SO2, fine particles (PM2.5), organic carbon (OC), and black carbon (BC) were 150.40, 6.70, 0.51, 0.88, 0.01, 0.13, 0.07, 0.43, 1.09, 0.34, and 0.06Tg, respectively, in 2012. Crop residue open burning emissions displayed typical seasonal and spatial variation. The highest emission regions were the Yellow-Huai River and Yangtse-Huai River areas, and the monthly emissions were highest in June (37%). Uncertainties in the emission estimates, measured as 95% confidence intervals, range from a low of within ±126% for N2O to a high of within ±169% for NH3.

  3. Global fire emission estimates (2007-2012) derived from inversion of formaldehyde columns

    NASA Astrophysics Data System (ADS)

    Bauwens, Maite; Stavrakou, Trissevgeni; Müller, Jean-Francois; De Smedt, Isabelle; Van Roozendael, Michel

    2014-05-01

    Wildfires have a strong impact on the chemistry and composition of the atmosphere and the radiative forcing. The fire emission estimates bear, however, important uncertainties due to the limited amount of field measurements, uncertainties in satellite burned area products, as well as empirical relations used for fuel type allocations. Atmospheric inversions are an alternative approach that provides new independent constraints on the fire estimates. This method involves measurements of trace gases combined with atmospheric models, where optimization algorithms are used to minimize the discrepancy between the model and the observations by adjusting the emission estimates. In this communication, we present global emission estimates of non-methane volatile organic compounds (NMVOCs), inferred from inversion of formaldehyde (HCHO) columns retrieved from the Global Ozone Monitoring Experiment-2 (GOME-2) instrument (De Smedt et al., 2012). The IMAGESv2 global CTM provides the relationship between the emissions and the vertical columns. The Global Fire Emissions Database version 3 (GFEDv3, van der Werf et al., 2010) is used as a priori bottom-up inventory in the model. The agreement between formaldehyde columns calculated by the IMAGESv2 model and the formaldehyde columns from GOME-2 is optimized using the adjoint modelling technique (Stavrakou et al., 2009). The obtained top-down fire emission estimates between 2007 and 2012 are available at the GlobEmission data portal (http://www.globemission.eu) on a monthly basis and at 0.5°x0.5° spatial resolution. The emission estimates are evaluated against three independent emission inventories: GFEDv3 (van der Werf et al., 2010), GFAS (Kaiser et al., 2012) and FINN (Wiedinmyer et al., 2011). Furthermore, simulated CO columns over the fire-affected regions will be compared with CO columns retrieved from the IASI sensor (George et al., 2009).

  4. Influence of bio-fuels on passenger car vehicle emissions

    NASA Astrophysics Data System (ADS)

    Petrea, M.; Kapernaum, M.; Wahl, C.

    2009-04-01

    In order to reduce the emissions of air pollutants, vehicles design and fuel formulation have changed. Ultra clean vehicle technologies started to be used in increased number. As a result, the emissions composition is expected to change as well. The use of new technologies and new fuels require new emissions tests especially for non-regulated compounds. The interest in using bio fuels as alternative fuels for petroleum-based ones has increased constantly in the last years. The advantages of the bio fuels usage is given by their similar proprieties, characteristics of renew ability, biodegradability and potential beneficial effects on the exhaust emission. The study involved measurements on a roller test facility of a reference passenger car representing new technologies (emission standards, injection system). The vehicle operated by use of reference gasoline and reference gasoline blended (10 and 20%) with bio-ethanol (EtOH). The measurements used different driving cycles: ARTEMIS cycle, real world driving cycle, NEDC cycle, the standard European driving cycle and additionally, a driving cycle consisting in Idle, 30, 50, 90 km/h. The sampling positions were before and after the catalyst and in the exhaust pipe. The detailed speciation of NMVOC' (non methane volatile organic compounds) was completed by use of active carbon tubes, DNPH (2,4-dinitrophenylhydrazine) tubes and cold traps. The particles were monitored by use of an on-line EEPS (Engine Exhaust Particle Sizer). CO2, NO, NO2 and NOX (NO +NO2) were continuously monitored by use of an on- line FTIR (Fourier transform infrared spectroscopy)- MEXA system. The investigations reveal that among the carbonylic compounds 15 oxygenated species were found in engine out exhaust and only 3 in tailpipe emissions, namely formaldehyde, acetaldehyde and acroleine. These are of great interest due to their impacts on human health. The hydrocarbons emissions decrease by increased of EtOH content. New compounds were observed

  5. 77 FR 31265 - Approval and Promulgation of Implementation Plans; Ohio; Volatile Organic Compound Emission...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-05-25

    ... AGENCY 40 CFR Part 52 Approval and Promulgation of Implementation Plans; Ohio; Volatile Organic Compound... (Ohio EPA) submitted several volatile organic compound (VOC) rules for approval into its State... stationary sources, storage of volatile organic liquids, industrial cleaning solvents, and flatwood...

  6. Volatile organic compounds in the Pearl River Delta: Identification of source regions and recommendations for emission-oriented monitoring strategies

    NASA Astrophysics Data System (ADS)

    Yuan, Zibing; Zhong, Liuju; Lau, Alexis Kai Hon; Yu, Jian Zhen; Louie, Peter K. K.

    2013-09-01

    For the purpose of systematically characterizing the ambient volatile organic compound (VOC) levels and their emission sources in the Pearl River Delta (PRD) of China, a grid study with VOC samples simultaneously taken at 84 sites over the PRD was conducted in summer and winter of 2008 and 2009. Positive Matrix Factorization (PMF) model was applied to identify the major VOC contributing sources and their temporal and spatial variations. Nine sources were identified, with gasoline exhaust, industrial emission and LPG leakage & propellant emission the top three significant sources. They accounted for 23%, 16% and 13% of the ambient VOC levels, respectively. Control measures should be therefore targeted on mitigating the VOC emissions from the traffic-related and industrial-related sources. The total VOC level did not show strong increase from 5 a.m. to 10 a.m. during all the four sampling campaigns, which may result from stronger wind and higher mixing height at 10 a.m. Three hotspot areas with significant VOC contributions were identified by source apportionment analysis: (1) the Pearl River Estuary; (2) an area from Central Dongguan to North Shenzhen; and (3) the Zhuhai-Zhongshan-Jiangmen area. For better characterizing the roles of VOC and NOx in producing the secondary pollutants and to identify specific sources emitting excessive concentrations of precursors, the emission-oriented Photochemical Assessment Monitoring Station (PAMS) network is recommended to be established in the PRD. Three PAMS networks are suggested in correspondence to the three identified hotspot areas.

  7. Direct green waste land application: How to reduce its impacts on greenhouse gas and volatile organic compound emissions?

    PubMed

    Zhu-Barker, Xia; Burger, Martin; Horwath, William R; Green, Peter G

    2016-06-01

    Direct land application as an alternative to green waste (GW) disposal in landfills or composting requires an understanding of its impacts on greenhouse gas (GHG) and volatile organic compound (VOC) emissions. We investigated the effects of two approaches of GW direct land application, surface application and soil incorporation, on carbon dioxide (CO2), nitrous oxide (N2O) and methane (CH4), and VOC emissions for a 12month period. Five treatments were applied in fall 2013 on fallow land under a Mediterranean climate in California: 30cm height GW on surface; 15cm height GW on surface; 15cm height GW tilled into soil; control+till; control+no till. In addition, a laboratory experiment was conducted to develop a mechanistic understanding of the influence of GW application on soil O2 consumption and GHG emission. The annual cumulative N2O, CO2 and VOC emissions ranged from 1.6 to 5.5kgN2O-Nha(-1), 5.3 to 40.6MgCO2-Cha(-1) and 0.6 to 9.9kgVOCha(-1), respectively, and were greatly reduced by GW soil incorporation compared to surface application. Application of GW quickly consumed soil O2 within one day in the lab incubation. These results indicate that to reduce GHG and VOC emissions of GW direct land application, GW incorporation into soil is recommended.

  8. Impact of intramolecular twisting and exciton migration on emission efficiency of multifunctional fluorene-benzothiadiazole-carbazole compounds

    NASA Astrophysics Data System (ADS)

    Karpicz, R.; Puzinas, S.; Krotkus, S.; Kazlauskas, K.; Jursenas, S.; Grazulevicius, J. V.; Grigalevicius, S.; Gulbinas, V.

    2011-05-01

    Novel donor-acceptor compounds consisting of singly bonded fluorene (Fl), benzothiadiazole (BT), and carbazole (Cz) functional units in the same molecule were investigated. Analysis of the optical spectra and fluorescence transients of the compounds revealed the domination of intramolecular charge transfer (ICT) states with high fluorescence quantum yield (72%-85%). A similar Cz-Fl-Cz compound exhibiting 100% fluorescence quantum yield and no ICT character was also studied as a reference to reveal the impact of electron-accepting BT groups. Thorough examination of the optical properties of the compounds in different media, i.e., dilute solution and polymer matrix, indicated their twisted conformations due to steric hindrance in the ground state and flattened geometry in the excited state for both reference and ICT compounds. Remarkable fluorescence efficiency losses (amounting to 70%) observed upon casting the molecular solutions into neat films were determined to originate from the low-fluorescent twisted conformers and migration-facilitated exciton quenching. The majority of emission efficiency losses (over 70%) were caused by the twisted conformers, whereas only less than 30% by exciton-migration-induced nonradiative deactivation.

  9. Volatile Organic Compound Concentrations and Emission Rates in New Manufactured and Site-Built Houses

    SciTech Connect

    Armin Rudd

    2008-10-30

    This study was conducted with the primary objective of characterizing and comparing the airborne concentrations and the emission rates of total VOCs and selected individual VOCs, including formaldehyde, among a limited number of new manufactured and site-built houses.

  10. Kinetic model of atomic and molecular emissions in laser-induced breakdown spectroscopy of organic compounds.

    PubMed

    Ma, Qianli; Dagdigian, Paul J

    2011-07-01

    A kinetic model previously developed to predict the relative intensities of atomic emission lines in laser-induced breakdown spectroscopy has been extended to include processes related to CN and C(2) molecular emissions. Simulations with this model were performed to predict the relative excited-state populations. The results from the simulations are compared with experimentally determined excited-state populations from 1,064 nm laser irradiation of organic residues on aluminum foil. The model reasonably predicts the relative intensity of the molecular emissions. Significantly, the model reproduces the vastly different temporal profiles of the atomic and molecular emissions. The latter are found to extend to much longer times after the laser pulse, and this appears to be due to the increasing concentration of the molecules versus time. From the simulations, the important processes affecting the CN and C(2) concentrations are identified.

  11. Final Report on Testing of Off-Gas Treatment Technologies for Abatement of Atmospheric Emissions of Chlorinated Volatile Organic Compounds

    SciTech Connect

    Jarosch, T.R.; Haselow, J.S.; Rossabi, J.; Burdick, S.A.; Raymond, R.; Young, J.E.; Lombard, K.H.

    1995-01-23

    The purpose of this report is to summarize the results of the program for off-gas treatment of atmospheric emissions of chlorinated volatile organic compounds (CVOCs), in particular trichloroethylene (TCE) and perchloroethylene (PCE). This program was funded through the Department of Energy Office of Technology Development`s VOC`s in Non-Arid Soils Integrated Demonstration (VNID). The off-gas treatment program was initiated after testing of in-situ air stripping with horizontal wells was completed (Looney et al., 1991). That successful test expectedly produced atmospheric emissions of CVOCs that were unabated. It was decided after that test that an off-gas treatment is an integral portion of remediation of CVOC contamination in groundwater and soil but also because several technologies were being developed across the United States to mitigate CVOC emissions. A single platform for testing off-gas treatment technologies would facilitate cost effective evaluation of the emerging technologies. Another motivation for the program is that many CVOCs will be regulated under the Clean Air Act Amendments of 1990 and are already regulated by many state regulatory programs. Additionally, compounds such as TCE and PCE are pervasive subsurface environmental contaminants, and, as a result, a small improvement in terms of abatement efficiency or cost will significantly reduce CVOC discharges to the environment as well as costs to United States government and industry.

  12. Detection of emission indices of aircraft exhaust compounds by open-path optical methods at airports

    NASA Astrophysics Data System (ADS)

    Schürmann, Gregor; Schäfer, Klaus; Jahn, Carsten; Hoffmann, Herbert; Utzig, Selina

    2005-10-01

    Air pollutant emission rates of aircrafts are determined with test bed measurements. Regulations exist for CO2, NO, NO2, CO concentrations, the content of total unburned hydrocarbons and the smoke number, a measure of soot. These emission indices are listed for each engine in a data base of the International Civil Aviation Organisation (ICAO) for four different Air pollutant emission rates of aircrafts are determined with test bed measurements. Regulations exist for CO2, NO, NO2, CO concentrations, the content of total unburned hydrocarbons and the smoke number, a measure of soot. These emission indices are listed for each engine in a data base of the International Civil Aviation Organisation (ICAO) for four different thrust levels (Idle, approach, cruise and take-off). It is a common procedure to use this data base as a starting point to estimate aircraft emissions at airports and further on to calculate the contribution of airports on local air quality. The comparison of these indices to real in use measurements therefore is a vital task to test the quality of air quality models at airports. Here a method to determine emission indices is used, where concentration measurements of CO2 together with other pollutants in the aircraft plume are needed. During intensive measurement campaigns at Zurich (ZRH) and Paris Charles De Gaulle (CDG) airports, concentrations of CO2, NO, NO2 and CO were measured. The measurement techniques were Fourier-Transform-Infrared (FTIR) spectrometry and Differential Optical Absorption Spectroscopy (DOAS). The big advantage of these methods is that no operations on the airport are influenced during measurement times. Together with detailed observations of taxiway movements, a comparison of emission indices with real in use emissions is possible.

  13. Volatile organic compound emissions from dairy cows and their waste as measured by proton-transfer-reaction mass spectrometry.

    PubMed

    Shaw, Stephanie L; Mitloehner, Frank M; Jackson, Wendi; Depeters, Edward J; Fadel, James G; Robinson, Peter H; Holzinger, Rupert; Goldstein, Allen H

    2007-02-15

    California dairies house approximately 1.8 million lactating and 1.5 million dry cows and heifers. State air regulatory agencies view these dairies as a major air pollutant source, but emissions data are sparse, particularly for volatile organic compounds (VOCs). The objective of this work was to determine VOC emissions from lactating and dry dairy cows and their waste using an environmental chamber. Carbon dioxide and methane were measured to provide context for the VOCs. VOCs were measured by proton-transfer-reaction mass spectrometry (PTR-MS). The compounds with highest fluxes when cows plus waste were present were methanol, acetone + propanal, dimethylsulfide, and m/z 109 (likely 4-methyl-phenol). The compounds with highest fluxes from fresh waste (urine and feces) were methanol, m/z 109, and m/z 60 (likely trimethylamine). Ethanol fluxes are reported qualitatively, and several VOCs that were likely emitted (formaldehyde, methylamine, dimethylamine) were not detectable by PTR-MS. The sum of reactive VOC fluxes measured when cows were present was a factor of 6-10 less than estimates historically used for regulatory purposes. In addition, ozone formation potentials of the dominant VOCs were -10% those of typical combustion or biogenic VOCs. Thus dairy cattle have a comparatively small impact on ozone formation per VOC mass emitted.

  14. Determination of volatile halogenated organic compounds in soils by purge-and-trap capillary gas chromatography with atomic emission detection.

    PubMed

    Campillo, Natalia; Viñas, Pilar; López-García, Ignacio; Aguinaga, Nerea; Hernández-Córdoba, Manuel

    2004-10-20

    Nine volatile halogenated organic compounds (VHOCs), including four trihalomethanes (THMs), were determined in soils by capillary gas chromatography with microwave induced-plasma atomic emission spectrometry (GC-AED), using a purge-and-trap system (PT) for sample preconcentration. Analytes were previously extracted from the soil sample in methanol and the extract was preconcentrated before being chromatographed. Element-specific detection and quantification were carried out monitoring two wavelength emission lines, corresponding to chlorine (479nm) and bromine (478nm). Each chromatographic run took 21min, including the purge step. The method showed a precision of 1.1-7.2% (R.S.D.) depending on the compound. Detection limits ranged from 0.05 to 0.55ngml(-1), for chloroform and dichloromethane, respectively, corresponding to 3.3 and 36.0ngg(-1) in the soil samples. The chromatographic profiles obtained showed no interference from co-extracted compounds. Low levels of dichloromethane and chloroform ranging from 0.04 to 1.13mugg(-1) were found in samples obtained from small gardens irrigated with tap water. The method is reliable and can be used for routine monitoring in soil samples.

  15. Biogenic volatile organic compound emissions from nine tree species used in an urban tree-planting program

    NASA Astrophysics Data System (ADS)

    Curtis, A. J.; Helmig, D.; Baroch, C.; Daly, R.; Davis, S.

    2014-10-01

    The biogenic volatile organic compound (BVOC) emissions of nine urban tree species were studied to assess the air quality impacts from planting a large quantity of these trees in the City and County of Denver, Colorado, through the Mile High Million tree-planting initiative. The deciduous tree species studied were Sugar maple, Ohio buckeye, northern hackberry, Turkish hazelnut, London planetree, American basswood, Littleleaf linden, Valley Forge elm, and Japanese zelkova. These tree species were selected using the i-Tree Species Selector (itreetools.org). BVOC emissions from the selected tree species were investigated to evaluate the Species Selector data under the Colorado climate and environmental growing conditions. Individual tree species were subjected to branch enclosure experiments in which foliar emissions of BVOC were collected onto solid adsorbent cartridges. The cartridge samples were analyzed for monoterpenes (MT), sesquiterpenes (SQT), and other C10-C15 BVOC using thermal desorption-gas chromatography-flame ionization detection/mass spectroscopy (GC-FID/MS). Individual compounds and their emission rates (ER) were identified. MT were observed in all tree species, exhibiting the following total MT basal emission rates (BER; with a 1-σ lower bound, upper bound uncertainty window): Sugar maple, 0.07 (0.02, 0.11) μg g-1 h-1; London planetree, 0.15 (0.02, 0.27) μg g-1 h-1; northern hackberry, 0.33 (0.09, 0.57) μg g-1 h-1; Japanese zelkova, 0.42 (0.26, 0.58) μg g-1 h-1; Littleleaf linden, 0.71 (0.33, 1.09) μg g-1 h-1; Valley Forge elm, 0.96 (0.01, 1.92) μg g-1 h-1; Turkish hazelnut, 1.30 (0.32, 2.23) μg g-1 h-1; American basswood, 1.50 (0.40, 2.70) μg g-1 h-1; and Ohio buckeye, 6.61 (1.76, 11.47) μg g-1 h-1. SQT emissions were seen in five tree species with total SQT BER of: London planetree, 0.11 (0.01, 0.20) μg g-1 h-1; Japanese zelkova, 0.11 (0.05, 0.16) μg g-1 h-1; Littleleaf linden, 0.13 (0.06, 0.21) μg g-1 h-1; northern hackberry, 0.20 (0

  16. [Development of vehicular emission inventory in China].

    PubMed

    Song, Xiang-yu; Xie, Shao-dong

    2006-06-01

    The vehicular emission inventories with high spatial resolution of 40km x 40km are developed using GIS technique based on the statistic data from yearbooks about vehicles and roads at provincial level in China for the year 2002, and on the emission factors calculated by COPERT III model for each category of vehicles in urban, rural and highway traffic. The results show that the emissions of CO, NOx, NMVOC and PM10 are 28.15, 3.05, 4.61 and 1.11 million tons, respectively, principally from motorcycles and gasoline passenger cars. The emissions concentrate on the developed areas and those from 10.8%, 2.2%, 9.7% and 5.3% of country acreage account for 84% of CO, 55% of NMVOC, 48% of NOx, 48% of PM10 emissions, respectively. The emissions in the east of China and coastal areas are higher than those in the west and hinterland areas. The emission source strengths in the Yangtze River Delta, the Pearl River Delta and Beijing & Tianjin area are the highest.

  17. Volatile organic compound emissions from the oil and natural gas industry in the Uintah Basin, Utah: oil and gas well pad emissions compared to ambient air composition

    NASA Astrophysics Data System (ADS)

    Warneke, C.; Geiger, F.; Edwards, P. M.; Dube, W.; Pétron, G.; Kofler, J.; Zahn, A.; Brown, S. S.; Graus, M.; Gilman, J. B.; Lerner, B. M.; Peischl, J.; Ryerson, T. B.; de Gouw, J. A.; Roberts, J. M.

    2014-10-01

    Emissions of volatile organic compounds (VOCs) associated with oil and natural gas production in the Uintah Basin, Utah were measured at a ground site in Horse Pool and from a NOAA mobile laboratory with PTR-MS instruments. The VOC compositions in the vicinity of individual gas and oil wells and other point sources such as evaporation ponds, compressor stations and injection wells are compared to the measurements at Horse Pool. High mixing ratios of aromatics, alkanes, cycloalkanes and methanol were observed for extended periods of time and for short-term spikes caused by local point sources. The mixing ratios during the time the mobile laboratory spent on the well pads were averaged. High mixing ratios were found close to all point sources, but gas well pads with collection and dehydration on the well pad were clearly associated with higher mixing ratios than other wells. The comparison of the VOC composition of the emissions from the oil and natural gas well pads showed that gas well pads without dehydration on the well pad compared well with the majority of the data at Horse Pool, and that oil well pads compared well with the rest of the ground site data. Oil well pads on average emit heavier compounds than gas well pads. The mobile laboratory measurements confirm the results from an emissions inventory: the main VOC source categories from individual point sources are dehydrators, oil and condensate tank flashing and pneumatic devices and pumps. Raw natural gas is emitted from the pneumatic devices and pumps and heavier VOC mixes from the tank flashings.

  18. Volatile organic compound emissions from straw-amended agricultural soils and their relations to bacterial communities: A laboratory study.

    PubMed

    Zhao, Juan; Wang, Zhe; Wu, Ting; Wang, Xinming; Dai, Wanhong; Zhang, Yujie; Wang, Ran; Zhang, Yonggan; Shi, Chengfei

    2016-07-01

    A laboratory study was conducted to investigate volatile organic compound (VOC) emissions from agricultural soil amended with wheat straw and their associations with bacterial communities for a period of 66days under non-flooded and flooded conditions. The results indicated that ethene, propene, ethanol, i-propanol, 2-butanol, acetaldehyde, acetone, 2-butanone, 2-pentanone and acetophenone were the 10 most abundant VOCs, making up over 90% of the total VOCs released under the two water conditions. The mean emission of total VOCs from the amended soils under the non-flooded condition (5924ng C/(kg·hr)) was significantly higher than that under the flooded condition (2211ng C/(kg·hr)). One "peak emission window" appeared at days 0-44 or 4-44, and over 95% of the VOC emissions occurred during the first month under the two water conditions. Bacterial community analysis using denaturing gradient gel electrophoresis (DGGE) showed that a relative increase of Actinobacteria, Bacteroidetes, Firmicutes and γ-Proteobacteria but a relative decrease of Acidobacteria with time were observed after straw amendments under the two water conditions. Cluster analysis revealed that the soil bacterial communities changed greatly with incubation time, which was in line with the variation of the VOC emissions over the experimental period. Most of the above top 10 VOCs correlated positively with the predominant bacterial species of Bacteroidetes, Firmicutes and Verrucomicrobia but correlated negatively with the dominant bacterial species of Actinobacteria under the two water conditions. These results suggested that bacterial communities might play an important role in VOC emissions from straw-amended agricultural soils.

  19. Carbonyl compound emissions from a heavy-duty diesel engine fueled with diesel fuel and ethanol-diesel blend.

    PubMed

    Song, Chonglin; Zhao, Zhuang; Lv, Gang; Song, Jinou; Liu, Lidong; Zhao, Ruifen

    2010-05-01

    This paper presents an investigation of the carbonyl emissions from a direct injection heavy-duty diesel engine fueled with pure diesel fuel (DF) and blended fuel containing 15% by volume of ethanol (E/DF). The tests have been conducted under steady-state operating conditions at 1200, 1800, 2600 rpm and idle speed. The experimental results show that acetaldehyde is the most predominant carbonyl, followed by formaldehyde, acrolein, acetone, propionaldehyde and crotonaldehyde, produced from both fuels. The emission factors of total carbonyls vary in the range 13.8-295.9 mg(kWh)(-1) for DF and 17.8-380.2mg(kWh)(-1) for E/DF, respectively. The introduction of ethanol into diesel fuel results in a decrease in acrolein emissions, while the other carbonyls show general increases: at low engine speed (1200 rpm), 0-55% for formaldehyde, 4-44% for acetaldehyde, 38-224% for acetone, and 5-52% for crotonaldehyde; at medium engine speed (1800 rpm), 106-413% for formaldehyde, 4-143% for acetaldehyde, 74-113% for acetone, 114-1216% for propionaldehyde, and 15-163% for crotonaldehyde; at high engine speed (2600 rpm), 36-431% for formaldehyde, 18-61% for acetaldehyde, 22-241% for acetone, and 6-61% for propionaldehyde. A gradual reduction in the brake specific emissions of each carbonyl compound from both fuels is observed with increase in engine load. Among three levels of engine speed employed, both DF and E/DF emit most CBC emissions at high engine speed. On the whole, the presence of ethanol in diesel fuel leads to an increase in aldehyde emissions.

  20. Plasma Source Development for Effective Dissociation and Abatement of Perfluorinated Compounds for the Reduction of Gas Emissions

    NASA Astrophysics Data System (ADS)

    Mahoney, Leonard J.

    2001-10-01

    Perfluorinated gas compounds (PFCs) are widely used in the semiconductor industry for etching process and for cleaning of chemical vapor deposition (CVD) systems. However, most of these compounds have very high infrared adsorbance strengths and long life times (i.e. several times greater than carbon dioxide). Thus their emissions can strongly contribute to global warming if left unabated. To reduce PFC emissions, the industry has adopted high power density, sub-atmospheric plasma sources to completely dissociate F-bearing compounds at the point of use or to completely convert PFC emissions within the post process exhaust stream. Many electrodeless plasma sources have been applied including microwave, conventional inductive, and ferrite-based inductive plasma devices. As a general scaling rule, most all of these devices provide effective electric field strengths on the order 1-10 V/cm and power densities of 0.1-10 W/cm3 into electronegative discharges at pressures ranging from 0.1-100 Torr. To explore one contemporary example, we examine the properties a ferrite-based, inductively-coupled plasma source as applied to typical processes used in CVD chamber clean and PFC-based etching processes. Along with the operational properties of this device, we examine mass spectroscopy measurements of residual gases from the source when used to (1) fully dissociate high flows of pure NF3 and mixtures of C3F8/O2 and (2) abate moderate flows of CF4, C2F6 and SF6 in combination with O2 or H2O vapor. Also, we review select plasma engineering topics related to these PFC abatement approaches whose study would greatly advance the performance and cost effectiveness of plasma abatement technology within the industry.

  1. A comprehensive emission inventory of biogenic volatile organic compounds in Europe: improved seasonality and land-cover

    NASA Astrophysics Data System (ADS)

    Oderbolz, D. C.; Aksoyoglu, S.; Keller, J.; Barmpadimos, I.; Steinbrecher, R.; Skjøth, C. A.; Plaß-Dülmer, C.; Prévôt, A. S. H.

    2013-02-01

    Biogenic volatile organic compounds (BVOC) emitted from vegetation are important for the formation of secondary pollutants such as ozone and secondary organic aerosols (SOA) in the atmosphere. Therefore, BVOC emission are an important input for air quality models. To model these emissions with high spatial resolution, the accuracy of the underlying vegetation inventory is crucial. We present a BVOC emission model that accommodates different vegetation inventories and uses satellite-based measurements of greenness instead of pre-defined vegetation periods. This approach to seasonality implicitly treats effects caused by water or nutrient availability, altitude and latitude on a plant stand. Additionally, we test the influence of proposed seasonal variability in enzyme activity on BVOC emissions. In its present setup, the emission model calculates hourly emissions of isoprene, monoterpenes, sesquiterpenes and the oxygenated volatile organic compounds (OVOC) methanol, formaldehyde, formic acid, ethanol, acetaldehyde, acetone and acetic acid. In this study, emissions based on three different vegetation inventories are compared with each other and diurnal and seasonal variations in Europe are investigated for the year 2006. Two of these vegetation inventories require information on tree-cover as an input. We compare three different land-cover inventories (USGS GLCC, GLC2000 and Globcover 2.2) with respect to tree-cover. The often-used USGS GLCC land-cover inventory leads to a severe reduction of BVOC emissions due to a potential miss-attribution of broad-leaved trees and reduced tree-cover compared to the two other land-cover inventories. To account for uncertainties in the land-cover classification, we introduce land-cover correction factors for each relevant land-use category to adjust the tree-cover. The results are very sensitive to these factors within the plausible range. For June 2006, total monthly BVOC emissions decreased up to -27% with minimal and increased

  2. Canopy light cues affect emission of constitutive and methyl jasmonate-induced volatile organic compounds in Arabidopsis thaliana

    PubMed Central

    Kegge, Wouter; Weldegergis, Berhane T; Soler, Roxina; Eijk, Marleen Vergeer-Van; Dicke, Marcel; Voesenek, Laurentius A C J; Pierik, Ronald

    2013-01-01

    The effects of plant competition for light on the emission of plant volatile organic compounds (VOCs) were studied by investigating how different light qualities that occur in dense vegetation affect the emission of constitutive and methyl-jasmonate-induced VOCs. Arabidopsis thaliana Columbia (Col-0) plants and Pieris brassicae caterpillars were used as a biological system to study the effects of light quality manipulations on VOC emissions and attraction of herbivores. VOCs were analysed using gas chromatography–mass spectrometry and the effects of light quality, notably the red : far red light ratio (R : FR), on expression of genes associated with VOC production were studied using reverse transcriptase–quantitative PCR. The emissions of both constitutive and methyl-jasmonate-induced green leaf volatiles and terpenoids were partially suppressed under low R : FR and severe shading conditions. Accordingly, the VOC-based preference of neonates of the specialist lepidopteran herbivore P. brassicae was significantly affected by the R : FR ratio. We conclude that VOC-mediated interactions among plants and between plants and organisms at higher trophic levels probably depend on light alterations caused by nearby vegetation. Studies on plant–plant and plant–insect interactions through VOCs should take into account the light quality within dense stands when extrapolating to natural and agricultural field conditions. PMID:23845065

  3. An investigation of the relationship between air emissions of volatile organic compounds and the incidence of cancer in Indiana counties.

    PubMed

    Boeglin, Michael L; Wessels, Denise; Henshel, Diane

    2006-02-01

    Cancer is a health endpoint influenced by a multitude of factors, including genetic history, individual behavior, and environmental insults. The ubiquity of toxicants in the environment has raised questions about the extent of their role in causing cancer in humans. More specifically, it is desirable to understand the cancer incidence due to airborne toxicants in anthropogenic pollution. One particular class of such pollutants is volatile organic compounds (VOCs). This paper reports an epidemiological investigation of the incidence of cancer in the 92 counties of Indiana. We evaluated the relationship between the amount of VOCs released in each county, as reported by the Toxic Release Inventory, and the county-by-county incidence of various types of cancer, especially those of less common organ systems not directly associated with the absorption or distribution of toxicants. Our evaluation considered chlorinated versus nonchlorinated emissions as well as stack versus fugitive emissions. We evaluated three models: linear, quadratic, and polynomial. Of these, the quadratic model appeared to be the best predictor (highest r2) for most endpoints for which there was a positive correlation. However, the linear model was the most sensitive (lowest P-value) for skin, melanoma, and endocrine-related cancers, including female genital system cancers. Our results indicate a relationship between emissions of VOCs and the incidence of some types of cancers. Most notable were strong correlations between VOC emissions and cancers of the brain, nervous system, endocrine system, and skin.

  4. Emission of volatile organic compounds from domestic coal stove with the actual alternation of flaming and smoldering combustion processes.

    PubMed

    Liu, Chengtang; Zhang, Chenglong; Mu, Yujing; Liu, Junfeng; Zhang, Yuanyuan

    2017-02-01

    Volatile organic compounds (VOCs) emissions from the chimney of a prevailing domestic stove fuelled with raw bituminous coal were measured under flaming and smoldering combustion processes in a farmer's house. The results indicated that the concentrations of VOCs quickly increased after the coal loading and achieved their peak values in a few minutes. The peak concentrations of the VOCs under the smoldering combustion process were significantly higher than those under the flaming combustion process. Alkanes accounted for the largest proportion (43.05%) under the smoldering combustion, followed by aromatics (28.86%), alkenes (21.91%), carbonyls (5.81%) and acetylene (0.37%). The emission factors of the total VOCs under the smoldering combustion processes (5402.9 ± 2031.8 mg kg(-1)) were nearly one order of magnitude greater than those under the flaming combustion processes (559.2 ± 385.9 mg kg(-1)). Based on the VOCs emission factors obtained in this study and the regional domestic coal consumption, the total VOCs emissions from domestic coal stoves was roughly estimated to be 1.25 × 10(8) kg a(-1) in the Beijing-Tianjin-Hebei region.

  5. Tracing the link between plant volatile organic compound emissions and CO2 fluxes and by stable isotopes

    NASA Astrophysics Data System (ADS)

    Werner, Christiane; Wegener, Frederik; Jardine, Kolby

    2015-04-01

    The vegetation exerts a large influence on the atmosphere through the emission of volatile organic compounds (VOCs) and the emission and uptake of the greenhouse gas CO2. Despite the enormous importance, processes controlling plant carbon allocation into primary and secondary metabolism, such as photosynthetic carbon uptake, respiratory CO2 emission and VOC synthesis, remains unclear. Moreover, vegetation-atmosphere CO2 exchange is associated with a large isotopic imprint due to photosynthetic carbon isotope discrimination and 13C-fractionation during respiratory CO2 release1. The latter has been proposed to be related to carbon partitioning in the metabolic branching points of the respiratory pathways and secondary metabolism, which are linked via a number of interfaces including the central metabolite pyruvate. Notably, it is a known substrate in a large array of secondary pathways leading to the biosynthesis of many volatile organic compounds (VOCs), such as volatile isoprenoids, oxygenated VOCs, aromatics, fatty acid oxidation products, which can be emitted by plants. Here we investigate the linkage between VOC emissions, CO2 fluxes and associated isotope effects based on simultaneous real-time measurements of stable carbon isotope composition of branch respired CO2 (CRDS) and VOC fluxes (PTR-MS). We utilized positionally specific 13C-labeled pyruvate branch feeding experiments in the mediterranean shrub (Halimium halimifolium) to trace the partitioning of C1, C2, and C3 carbon atoms of pyruvate into VOCs versus CO2 emissions in the light and in the dark. In the light, we found high emission rates of a large array of VOC including volatile isoprenoids, oxygenated VOCs, green leaf volatiles, aromatics, sulfides, and nitrogen containing VOCs. These observations suggest that in the light, H. halimifolium dedicates a high carbon flux through secondary biosynthetic pathways including the pyruvate dehydrogenase bypass, mevalonic acid, MEP/DOXP, shikimic acid, and

  6. Fungal succession in relation to volatile organic compounds emissions from Scots pine and Norway spruce leaf litter-decomposing fungi

    NASA Astrophysics Data System (ADS)

    Isidorov, Valery; Tyszkiewicz, Zofia; Pirożnikow, Ewa

    2016-04-01

    Leaf litter fungi are partly responsible for decomposition of dead material, nutrient mobilization and gas fluxes in forest ecosystems. It can be assumed that microbial destruction of dead plant materials is an important source of volatile organic compounds (VOCs) emitted into the atmosphere from terrestrial ecosystems. However, little information is available on both the composition of fungal VOCs and their producers whose community can be changed at different stages of litter decomposition. The fungal community succession was investigated in a litter bag experiment with Scots pine (Pinus sylvestris) and Norway spruce (Picea abies) needle litter. The succession process can be divided into a several stages controlled mostly by changes in litter quality. At the very first stages of decomposition the needle litter was colonized by ascomycetes which can use readily available carbohydrates. At the later stages, the predominance of Trichoderma sp., the known producers of cellulolytic enzymes, was documented. To investigate the fungi-derived VOCs, eight fungi species were isolated. As a result of gas chromatographic analyses, as many as 75C2sbnd C15 fungal volatile compounds were identified. Most components detected in emissions were very reactive substances: the principal groups of VOCs were formed by monoterpenes, carbonyl compounds and aliphatic alcohols. It was found that production of VOCs by fungi is species specific: only 10 metabolites were emitted into the gas phase by all eight species. The reported data confirm that the leave litter decomposition is important source of reactive organic compounds under the forest canopy.

  7. Historic records of organic compounds from a high Alpine glacier: influences of biomass burning, anthropogenic emissions, and dust transport

    NASA Astrophysics Data System (ADS)

    Müller-Tautges, C.; Eichler, A.; Schwikowski, M.; Pezzatti, G. B.; Conedera, M.; Hoffmann, T.

    2016-01-01

    Historic records of α-dicarbonyls (glyoxal, methylglyoxal), carboxylic acids (C6-C12 dicarboxylic acids, pinic acid, p-hydroxybenzoic acid, phthalic acid, 4-methylphthalic acid), and ions (oxalate, formate, calcium) were determined with annual resolution in an ice core from Grenzgletscher in the southern Swiss Alps, covering the time period from 1942 to 1993. Chemical analysis of the organic compounds was conducted using ultra-high-performance liquid chromatography (UHPLC) coupled to electrospray ionization high-resolution mass spectrometry (ESI-HRMS) for dicarbonyls and long-chain carboxylic acids and ion chromatography for short-chain carboxylates. Long-term records of the carboxylic acids and dicarbonyls, as well as their source apportionment, are reported for western Europe. This is the first study comprising long-term trends of dicarbonyls and long-chain dicarboxylic acids (C6-C12) in Alpine precipitation. Source assignment of the organic species present in the ice core was performed using principal component analysis. Our results suggest biomass burning, anthropogenic emissions, and transport of mineral dust to be the main parameters influencing the concentration of organic compounds. Ice core records of several highly correlated compounds (e.g., p-hydroxybenzoic acid, pinic acid, pimelic, and suberic acids) can be related to the forest fire history in southern Switzerland. P-hydroxybenzoic acid was found to be the best organic fire tracer in the study area, revealing the highest correlation with the burned area from fires. Historical records of methylglyoxal, phthalic acid, and dicarboxylic acids adipic acid, sebacic acid, and dodecanedioic acid are comparable with that of anthropogenic emissions of volatile organic compounds (VOCs). The small organic acids, oxalic acid and formic acid, are both highly correlated with calcium, suggesting their records to be affected by changing mineral dust transport to the drilling site.

  8. Ambient Concentrations and Emissions of a Comprehensive Suite of Volatile Organic Compounds at the CalNex-Bakersfield Supersite

    NASA Astrophysics Data System (ADS)

    Gentner, D. R.; Goldstein, A. H.

    2010-12-01

    Ambient concentrations of ~250 Volatile Organic Compounds (VOCs) were measured hourly via in-situ gas chromatography at the Bakersfield, CA supersite in May & June 2010 as part of the California at the Nexus between Air Quality and Climate Change (CalNex) Experiment. Measurements included anthropogenic and biogenic VOCs containing 1 to 17 carbon atoms and a variety of functional groups (e.g. aldehydes, ketones, alcohols, halogens, sulfur, & nitrogen). We quantified a very broad range of primary gas-phase organics that lead to the formation of secondary organic aerosol (SOA) and tropospheric ozone, and we also observed many gas-phase products of VOC photooxidation. Many of the observed VOCs are volatile and have been measured previously, but in this experiment we tailored the instrumentation to also measure compounds in the intermediate volatility range, which are thought to contribute significantly to SOA and have rarely or never been reported from in-situ measurements. Among the observed gas-phase VOCs with lower volatility are PAHs (e.g. naphthalene, methylnaphthalenes, and dimethylnaphthalenes), alkanes up to 17 carbon atoms, aromatics and cycloalkanes with multiple alkyl groups, and functionalized VOCs with lower volatility. Analyses of the diurnal variability, covariance between compounds, weekday/weekend differences, and statistical analyses for source apportionment such as Positive Matrix Factorization (PMF) will be utilized to establish the major sources of these compounds and estimate regional emissions. Our VOC data provides excellent context for analysis of the broad array of gas and particle phase measurements during CalNex2010, which will be used to elucidate the chemistry leading to formation of SOA and tropospheric ozone in this polluted region of California with diverse urban, industrial, agricultural, and natural emission sources.

  9. Emissions of nitrogen-containing organic compounds from the burning of herbaceous and arboraceous biomass: Fuel composition dependence and the variability of commonly used nitrile tracers

    NASA Astrophysics Data System (ADS)

    Coggon, Matthew M.; Veres, Patrick R.; Yuan, Bin; Koss, Abigail; Warneke, Carsten; Gilman, Jessica B.; Lerner, Brian M.; Peischl, Jeff; Aikin, Kenneth C.; Stockwell, Chelsea E.; Hatch, Lindsay E.; Ryerson, Thomas B.; Roberts, James M.; Yokelson, Robert J.; Gouw, Joost A.

    2016-09-01

    Volatile organic compounds (VOCs) emitted from residential wood and crop residue burning were measured in Colorado, U.S. When compared to the emissions from crop burning, residential wood burning exhibited markedly lower concentrations of acetonitrile, a commonly used biomass burning tracer. For both herbaceous and arboraceous fuels, the emissions of nitrogen-containing VOCs (NVOCs) strongly depend on the fuel nitrogen content; therefore, low NVOC emissions from residential wood burning result from the combustion of low-nitrogen fuel. Consequently, the emissions of compounds hazardous to human health, such as HNCO and HCN, and the formation of secondary pollutants, such as ozone generated by NOx, are likely to depend on fuel nitrogen. These results also demonstrate that acetonitrile may not be a suitable tracer for domestic burning in urban areas. Wood burning emissions may be best identified through analysis of the emissions profile rather than reliance on a single tracer species.

  10. Assessment of Volatile Organic Compound and Hazardous Air Pollutant Emissions from Oil and Natural Gas Well Pads using Mobile Remote and On-site Direct Measurements

    EPA Science Inventory

    Emissions of volatile organic compounds (VOC) and hazardous air pollutants (HAP) from oil and natural gas production were investigated using direct measurements of component-level emissions on well pads in the Denver-Julesburg (DJ) Basin and remote measurements of production pad-...

  11. Emissions of terpenoids, benzenoids, and other biogenic gas-phase organic compounds from agricultural crops and their potential implications for air quality

    NASA Astrophysics Data System (ADS)

    Gentner, D. R.; Ormeño, E.; Fares, S.; Ford, T. B.; Weber, R.; Park, J.-H.; Brioude, J.; Angevine, W. M.; Karlik, J. F.; Goldstein, A. H.

    2013-11-01

    Agriculture comprises a substantial fraction of land cover in many regions of the world, including California's San Joaquin Valley, which is out of compliance with state and federal standards for tropospheric ozone and particulate matter (PM2.5). Emissions from vegetation and other biogenic and anthropogenic sources react in the atmosphere to produce ozone and secondary organic aerosol, which comprises a substantial fraction of PM2.5. Using data from three measurement campaigns, we examine emissions of reactive gas-phase organic carbon from agricultural crops and their potential to impact regional air quality relative to anthropogenic emissions in California's San Joaquin Valley. Emission rates for a suite of biogenic terpenoid compounds were measured in a greenhouse for 25 representative crops from California in 2008, and ambient measurements of terpenoids and other biogenic compounds in the volatile and intermediate-volatility organic compound range were made over an orange orchard in a rural area of the San Joaquin Valley during two seasons in 2010: summer and spring flowering. When accounting for both emissions of reactive precursors and the deposition of ozone to an orange orchard, the net effect of the orange trees is a net source of ozone in the springtime during flowering, and relatively neutral for most of the summer until the fall when it becomes a sink. Flowering was a major emission event and caused a large increase in emissions including a suite of compounds that had not been measured in the atmosphere before. Such biogenic emission events need to be better parameterized in models as they have significant potential to impact regional air quality since emissions increase by an order of magnitude. In regions like the San Joaquin Valley, the mass of biogenic emissions from agricultural crops during the summer (without flowering) and the potential ozone and secondary organic aerosol formation from these emissions are on the same order as anthropogenic

  12. Emission of volatile organic compounds as affected by feedlot location, moisture, and temperature

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This study investigated the effects within pen location, moisture, and temperature on odor emission from manure resulting from a diet containing 30% wet distillers grain with solubles. Pen surface material was collected from three locations. Material from each pen was consolidated for each specific...

  13. Acoustic emission analysis as a non-destructive test procedure for fiber compound structures

    NASA Technical Reports Server (NTRS)

    Block, J.

    1983-01-01

    The concept of acoustic emission analysis is explained in scientific terms. The detection of acoustic events, their localization, damage discrimination, and event summation curves are discussed. A block diagram of the concept of damage-free testing of fiber-reinforced synthetic materials is depicted. Prospects for application of the concept are assessed.

  14. Large Drought-Induced Variations in Oak Leaf Volatile Organic Compound Emissions during PINOT NOIR 2012

    EPA Science Inventory

    Leaf-level isoprene and monoterpene emissions were collected and analyzed from five of the most abundant oak (Quercus) species in Central Missouri’s Ozarks Region in 2012 during PINOT NOIR (Particle Investigations at a Northern Ozarks Tower ‐ NOx, Oxidants, Isoprene Research). Ju...

  15. Volatile Organic Compound Emission from Quercus suber, Quercus canariensis, and its hybridisation product Quercus afares

    NASA Astrophysics Data System (ADS)

    Welter, S.; Bracho Nuñez, A.; Staudt, M.; Kesselmeier, J.

    2009-04-01

    Oaks represent one of the most important plant genera in the Northern hemisphere and include many intensively VOC emitting species. The major group constitutes the isoprene emitters, but also monoterpene emitters and non-emitters can be found. These variations in the oak species might partly be due to their propensity for inter- and intraspecific hybridisation. This study addresses the foliar VOC production of the former hybridisation product the deciduous Quercus afares and its parents, two very distant species: the evergreen monoterpene emitter Quercus suber and the deciduous isoprene emitter Quercus canariensis. The measurements were performed in Southern France, applying two different methods. Plants were investigated in situ in the field with a portable gas exchange measuring system as well as in the laboratory on cut branches with an adapted enclosure system. Quercus afares was found to be a monoterpene emitting species. However, the monoterpene emission was lower and the composition different to that of Quercus suber. Whereas Quercus suber trees belonged to the pinene type most individuals of Quercus afares were identified to represent a limonene type. Quercus canariensis emitted besides high amounts of isoprene also linalool and (Z)-3-hexenylacetate. Emissions from Quercus suber and Quercus afares were higher in the field measurements than in the laboratory on cut branches whereas Quercus canariensis exhibited lower isoprene emissions from cut branches. The results demonstrate the need of further emission studies on a plant species level.

  16. VARIATIONS IN THE EMISSIONS OF VOLATILE ORGANIC COMPOUNDS FROM THE TONER FROM A SPECIFIC PHOTOCOPIER

    EPA Science Inventory

    A laboratory thermal desorption apparatus was used to measure emissions from a number of nominally identical photocopier toners - manufactured for use in a specific model copier - when these toners were heated to fuser temperature (180 - 200 degrees C). The objective was to deter...

  17. The effect of warming and enhanced ultraviolet radiation on gender-specific emissions of volatile organic compounds from European aspen.

    PubMed

    Maja, Mengistu M; Kasurinen, Anne; Holopainen, Toini; Julkunen-Tiitto, Riitta; Holopainen, Jarmo K

    2016-03-15

    Different environmental stress factors often occur together but their combined effects on plant secondary metabolism are seldom considered. We studied the effect of enhanced ultraviolet (UV-B) (31% increase) radiation and temperature (ambient +2 °C) singly and in combination on gender-specific emissions of volatile organic compounds (VOCs) from 2-year-old clones of European aspen (Populus tremula L.). Plants grew in 36 experimental plots (6 replicates for Control, UV-A, UV-B, T, UV-A+T and UV-B+T treatments), in an experimental field. VOCs emitted from shoots were sampled from two (1 male and 1 female) randomly selected saplings (total of 72 saplings), per plot on two sampling occasions (June and July) in 2014. There was a significant UV-B×temperature interaction effect on emission rates of different VOCs. Isoprene emission rate was increased due to warming, but warming also modified VOC responses to both UV-A and UV-B radiation. Thus, UV-A increased isoprene emissions without warming, whereas UV-B increased emissions only in combination with warming. Warming-modified UV-A and UV-B responses were also seen in monoterpenes (MTs), sesquiterpenes (SQTs) and green leaf volatiles (GLVs). MTs showed also a UV × gender interaction effect as females had higher emission rates under UV-A and UV-B than males. UV × gender and T × gender interactions caused significant differences in VOC blend as there was more variation (more GLVs and trans-β-caryophyllene) in VOCs from female saplings compared to male saplings. VOCs from the rhizosphere were also collected from each plot in two exposure seasons, but no significant treatment effects were observed. Our results suggest that simultaneous warming and elevated-UV-radiation increase the emission of VOCs from aspen. Thus the contribution of combined environmental factors on VOC emissions may have a greater impact to the photochemical reactions in the atmosphere compared to the impact of individual factors acting alone.

  18. Volatile organic compounds from vegetation in southern Yunnan Province, China: Emission rates and some potential regional implications

    NASA Astrophysics Data System (ADS)

    Geron, Chris; Owen, Sue; Guenther, Alex; Greenberg, Jim; Rasmussen, Rei; Hui Bai, Jian; Li, Qing-Jun; Baker, Brad

    Little information is currently available regarding emissions of biogenic volatile organic compounds (BVOCs) in southern Asia. To address the need for BVOC emission estimates in regional atmospheric chemistry simulations, 95 common plant species were screened for emissions of BVOC in and near the Xishuangbanna Tropical Biological Gardens in southern Yunnan Province, Peoples' Republic of China in February 2003. In situ measurements with leaf cuvettes and branch bag enclosures were used in combination with portable gas chromatography, flame ionization, photoionization, and mass spectral detection to identify and quantify BVOC emissions. Forty-four of the species examined emitted isoprene at rates exceeding 20 μg C g -1 (leaf dry weight) h -1. An emphasis was placed on the genus Ficus, which is important in the region and occupies a wide range of ecological niches. Several species in the footprint of a nearby flux tower were also examined. Several palm species and an abundant fern ( Cyclosorus parasiticus) emitted substantial amounts of isoprene, and probably accounted for observed daytime mean isoprene fluxes from the understory of a Hevea brasiliensis plantation of 1.0 and 0.15 mg C m -2 h -1 during the wet and dry seasons, respectively. These measurements verify that both the forest floor and canopy in this region can be sources of isoprene. Monoterpene emissions exceeded 1.0 μg-C g -1 (leaf dry weight) h -1 from only 4 of 38 species surveyed, including some Ficus species and H. brasiliensis. However most of the trees of the latter species were sparsely foliated due to dry season senescence, and emission factors are approximately an order of magnitude lower than those reported during the wet season. BVOC emission rates and physiology of many species are impacted by reduced moisture availability, especially Mangifera indica. South Asia is a region undergoing rapid landuse change and forest plantation establishment, with large increases in area of high BVOC

  19. Halocarbon emissions by selected tropical seaweeds: species-specific and compound-specific responses under changing pH.

    PubMed

    Mithoo-Singh, Paramjeet Kaur; Keng, Fiona S-L; Phang, Siew-Moi; Leedham Elvidge, Emma C; Sturges, William T; Malin, Gill; Abd Rahman, Noorsaadah

    2017-01-01

    Five tropical seaweeds, Kappaphycus alvarezii (Doty) Doty ex P.C. Silva, Padina australis Hauck, Sargassum binderi Sonder ex J. Agardh (syn. S. aquifolium (Turner) C. Agardh), Sargassum siliquosum J. Agardh and Turbinaria conoides (J. Agardh) Kützing, were incubated in seawater of pH 8.0, 7.8 (ambient), 7.6, 7.4 and 7.2, to study the effects of changing seawater pH on halocarbon emissions. Eight halocarbon species known to be emitted by seaweeds were investigated: bromoform (CHBr3), dibro-momethane (CH2Br2), iodomethane (CH3I), diiodomethane (CH2I2), bromoiodomethane (CH2BrI), bromochlorometh-ane (CH2BrCl), bromodichloromethane (CHBrCl2), and dibro-mochloromethane (CHBr2Cl). These very short-lived halocarbon gases are believed to contribute to stratospheric halogen concentrations if released in the tropics. It was observed that the seaweeds emit all eight halocarbons assayed, with the exception of K. alvarezii and S. binderi for CH2I2 and CH3I respectively, which were not measurable at the achievable limit of detection. The effect of pH on halocarbon emission by the seaweeds was shown to be species-specific and compound specific. The highest percentage changes in emissions for the halocarbons of interest were observed at the lower pH levels of 7.2 and 7.4 especially in Padina australis and Sargassum spp., showing that lower seawater pH causes elevated emissions of some halocarbon compounds. In general the seaweed least affected by pH change in terms of types of halocarbon emission, was P. australis. The commercially farmed seaweed K. alvarezii was very sensitive to pH change as shown by the high increases in most of the compounds in all pH levels relative to ambient. In terms of percentage decrease in maximum quantum yield of photosynthesis (Fv∕Fm) prior to and after incubation, there were no significant correlations with the various pH levels tested for all seaweeds. The correlation between percentage decrease in the maximum quantum yield of photosynthesis (Fv

  20. Halocarbon emissions by selected tropical seaweeds: species-specific and compound-specific responses under changing pH

    PubMed Central

    Leedham Elvidge, Emma C.; Sturges, William T.; Malin, Gill; Abd Rahman, Noorsaadah

    2017-01-01

    Five tropical seaweeds, Kappaphycus alvarezii (Doty) Doty ex P.C. Silva, Padina australis Hauck, Sargassum binderi Sonder ex J. Agardh (syn. S. aquifolium (Turner) C. Agardh), Sargassum siliquosum J. Agardh and Turbinaria conoides (J. Agardh) Kützing, were incubated in seawater of pH 8.0, 7.8 (ambient), 7.6, 7.4 and 7.2, to study the effects of changing seawater pH on halocarbon emissions. Eight halocarbon species known to be emitted by seaweeds were investigated: bromoform (CHBr3), dibro­momethane (CH2Br2), iodomethane (CH3I), diiodomethane (CH2I2), bromoiodomethane (CH2BrI), bromochlorometh­ane (CH2BrCl), bromodichloromethane (CHBrCl2), and dibro­mochloromethane (CHBr2Cl). These very short-lived halocarbon gases are believed to contribute to stratospheric halogen concentrations if released in the tropics. It was observed that the seaweeds emit all eight halocarbons assayed, with the exception of K. alvarezii and S. binderi for CH2I2 and CH3I respectively, which were not measurable at the achievable limit of detection. The effect of pH on halocarbon emission by the seaweeds was shown to be species-specific and compound specific. The highest percentage changes in emissions for the halocarbons of interest were observed at the lower pH levels of 7.2 and 7.4 especially in Padina australis and Sargassum spp., showing that lower seawater pH causes elevated emissions of some halocarbon compounds. In general the seaweed least affected by pH change in terms of types of halocarbon emission, was P. australis. The commercially farmed seaweed K. alvarezii was very sensitive to pH change as shown by the high increases in most of the compounds in all pH levels relative to ambient. In terms of percentage decrease in maximum quantum yield of photosynthesis (Fv∕Fm) prior to and after incubation, there were no significant correlations with the various pH levels tested for all seaweeds. The correlation between percentage decrease in the maximum quantum yield of photosynthesis

  1. Volatile organic compound emissions from different stages of Cananga odorata flower development.

    PubMed

    Qin, Xiao-Wei; Hao, Chao-Yun; He, Shu-Zhen; Wu, Gang; Tan, Le-He; Xu, Fei; Hu, Rong-Suo

    2014-06-27

    Headspace-solid phase microextraction-gas chromatography-mass spectrometry (HS-SPME-GC-MS) was used to identify the volatile organic compounds (VOCs) of the different flower development stages of Cananga odorata for the evaluation of floral volatile polymorphism as a basis to determine the best time of harvest. Electronic nose results, coupled with discriminant factor analysis, suggested that emitted odors varied in different C. odorata flower development stages, including the bud, display-petal, initial-flowering, full-flowering, end-flowering, wilted-flower, and dried flower stages. The first two discriminant factors explained 97.52% of total system variance. Ninety-two compounds were detected over the flower life, and the mean Bray-Curtis similarity value was 52.45% among different flower development stages. A high level of volatile polymorphism was observed during flower development. The VOCs were largely grouped as hydrocarbons, esters, alcohols, aldehydes, phenols, acids, ketones, and ethers, and the main compound was β-caryophyllene (15.05%-33.30%). Other identified compounds were β-cubebene, D-germacrene, benzyl benzoate, and α-cubebene. Moreover, large numbers of VOCs were detected at intermediate times of flower development, and more hydrocarbons, esters, and alcohols were identified in the full-flowering stage. The full-flowering stage may be the most suitable period for C. odorata flower harvest.

  2. Reducing Emissions of Volatile Organic Compounds - Final Report - 08/15/1997 - 02/14/2001

    SciTech Connect

    Stensel, H. David; Strand, Stuart E.

    2001-03-14

    The overall objective of this research was to determine if the shallow suspended growth reactor (SSGR) could provide sufficient treatment performance of organic and reduced sulfur (TRS) compounds, at 50 C to meet the EPA ''cluster rule'' regulatory limits. The biodegradation of a mixture of organic compounds that could be present in pulp and paper high volume low concentration gas streams was evaluated at 50 C in a bench-scale SSGR. The removal of methanol was followed in particular, and was mathematically modeled to evaluate the effect of process design and operating parameters on methanol removal. Additional tests were performed to obtain mass transfer and biodegradation kinetic parameters for the model. The acclimation of microbial populations capable of degrading TRS compounds from various seed sources was studied in batch reactors at 30 and 50 C. The degradation of TRS compounds in bench-scale SSGR was studied at 20-50 C. Also, the biodegradation kinetic and mass transfer coefficients for alpha-terpinene and gamma-terpinene were studied. Finally, a pilot plant was constructed and operated at Simpson pulp and paper mill in Tacoma, WA.

  3. CHARACTERIZATION OF EMISSIONS OF VOLATILE ORGANIC COMPOUNDS FROM INTERIOR ALKYD PAINT

    EPA Science Inventory

    Alkyd paint continues to be used indoors for application to wood trim, cabinet surfaces, and some kitchen and bathroom walls. Paint may represent a significant source of volatile organic compounds (VOCs) indoors depending on the frequency of use and amount of surface paint. The U...

  4. Dimethoxymethane in Diesel Fuel: Chemical Characterization of Toxicologically Relevart Compounds From Diesel Emissions

    DTIC Science & Technology

    2001-04-01

    then compounds relevant to the use of this chemical would need to be measured including, but not limited to urea, ammonia, biuret , and cyanic acid. 3.0...Combustion heat release analysis reveals reactions that occur BTDC, with long in-cylinder residence time of the pilot injected fuel. Differences in

  5. Process-specific emission characteristics of volatile organic compounds (VOCs) from petrochemical facilities in the Yangtze River Delta, China.

    PubMed

    Mo, Ziwei; Shao, Min; Lu, Sihua; Qu, Hang; Zhou, Mengyi; Sun, Jin; Gou, Bin

    2015-11-15

    Process-specific emission characteristics of volatile organic compounds (VOCs) from petrochemical facilities were investigated in the Yangtze River Delta, China. Source samples were collected from various process units in the petrochemical, basic chemical, and chlorinated chemical plants, and were measured using gas chromatography-mass spectrometry/flame ionization detection. The results showed that propane (19.9%), propene (11.7%), ethane (9.5%) and i-butane (9.2%) were the most abundant species in the petrochemical plant, with propene at much higher levels than in petrochemical profiles measured in other regions. Styrene (15.3%), toluene (10.3%) and 1,3-butadiene (7.5%) were the major species in the basic chemical industry, while halocarbons, especially dichloromethane (15.2%) and chloromethane (7.5%), were substantial in the chlorinated chemical plant. Composite profiles were calculated using a weight-average approach based on the VOC emission strength of various process units. Emission profiles for an entire petrochemical-related industry were found to be process-oriented and should be established considering the differences in VOC emissions from various manufacturing facilities. The VOC source reactivity and carcinogenic risk potential of each process unit were also calculated in this study, suggesting that process operations mainly producing alkenes should be targeted for possible controls with respect to reducing the ozone formation potential, while process units emitting 1,3-butadiene should be under priority control in terms of toxicity. This provides a basis for further measurements of process-specific VOC emissions from the entire petrochemical industry. Meanwhile, more representative samples should be collected to reduce the large uncertainties.

  6. Screening the Emission Sources of Volatile Organic Compounds (VOCs) in China Based on Multi-effect Evaluation

    NASA Astrophysics Data System (ADS)

    Niu, H., Jr.

    2015-12-01

    Volatile organic compounds (VOCs) in the atmosphere have adverse impacts via three main pathways: photochemical ozone formation, secondary organic aerosol production, and direct toxicity to humans. Few studies have integrated these effects to prioritize control measures for VOCs sources. In this study, we developed a multi-effect evaluation methodology based on updated emission inventories and source profiles, which was combined with ozone formation potential (OFP), secondary organic aerosol potential (SOAP), and VOC toxicity data to identify important emission sources and key species. We derived species-specific emission inventories for 152 sources. The OFPs, SOAPs, and toxicity of each source were determined, and the contribution and share of each source to each of these adverse effects was calculated. Weightings were given to the three adverse effects by expert scoring, and the integrated impact was determined. Using 2012 as the base year, solvent usage and industrial process were found to be the most important anthropogenic sources, accounting for 24.2 and 23.1% of the integrated environmental effect, respectively. This was followed by biomass burning, transportation, and fossil fuel combustion, all of which had a similar contribution ranging from 16.7 to 18.6%. The top five industrial sources, including plastic products, rubber products, chemical fiber products, the chemical industry, and oil refining, accounted for nearly 70.0% of industrial emissions. In China, emissions reductions are required for styrene, toluene, ethylene, benzene, and m/p-xylene. The 10 most abundant chemical species contributed 76.5% of the integrated impact. Beijing, Chongqing, Shanghai, Jiangsu, and Guangdong were the five leading provinces when considering the integrated effects. Besides, the chemical mass balance model (CMB) was used to verify the VOCs inventories of 47 cities in China, so as to optimize our evaluation results. We suggest that multi-effect evaluation is necessary to

  7. Microbial communities related to volatile organic compound emission in automobile air conditioning units.

    PubMed

    Diekmann, Nina; Burghartz, Melanie; Remus, Lars; Kaufholz, Anna-Lena; Nawrath, Thorben; Rohde, Manfred; Schulz, Stefan; Roselius, Louisa; Schaper, Jörg; Mamber, Oliver; Jahn, Dieter; Jahn, Martina

    2013-10-01

    During operation of mobile air conditioning (MAC) systems in automobiles, malodours can occur. We studied the microbial communities found on contaminated heat exchanger fins of 45 evaporators from car MAC systems which were operated in seven different regions of the world and identified corresponding volatile organic compounds. Collected biofilms were examined by scanning electron microscopy and fluorescent in situ hybridization. The detected bacteria were loosely attached to the metal surface. Further analyses of the bacteria using PCR-based single-strand conformation polymorphism and sequencing of isolated 16S rRNA gene fragments identified highly divergent microbial communities with multiple members of the Alphaproteobacteriales, Methylobacteria were the prevalent bacteria. In addition, Sphingomonadales, Burkholderiales, Bacillales, Alcanivorax spp. and Stenotrophomonas spp. were found among many others depending on the location the evaporators were operated. Interestingly, typical pathogenic bacteria related to air conditioning systems including Legionella spp. were not found. In order to determine the nature of the chemical compounds produced by the bacteria, the volatile organic compounds were examined by closed loop stripping analysis and identified by combined gas chromatography/mass spectrometry. Sulphur compounds, i.e. di-, tri- and multiple sulphides, acetylthiazole, aromatic compounds and diverse substituted pyrazines were detected. Mathematical clustering of the determined microbial community structures against their origin identified a European/American/Arabic cluster versus two mainly tropical Asian clusters. Interestingly, clustering of the determined volatiles against the origin of the corresponding MAC revealed a highly similar pattern. A close relationship of microbial community structure and resulting malodours to the climate and air quality at the location of MAC operation was concluded.

  8. Determination of ratios of Auger electrons emission probabilities and K-L shell vacancy transfer probability of Cr, Mn, Fe, Co, Ni, Cu and Zn compounds

    NASA Astrophysics Data System (ADS)

    Küçükönder, Adnan; Kavşut, Onur

    2017-02-01

    Ratios of emission probabilities of Auger electrons [u = p(KLX)/p(KLL), ν = p(KXY)/p(KLL)] and the vacancy transfer probabilities from K to L shell, ηKL for Cr, Mn, Fe, Co,Ni, Cu and Zn compounds were obtained using the experimental Kx-ray emission ratios and K-shell fluorescence yields. We were used the experimental Kβ/Kα intensity ratios and K shell fluorescence yields WK. Ratios of emission probabilities of Auger electrons and the vacancy transfer probabilities are changed by chemical effect for different for Cr, Mn, Fe, Co,Ni, Cu and Zn compounds.

  9. Emission and Chemistry of Volatile Organic Compounds (VOCs) as Observed at T3: Contrast of the Dry and Wet Seasons

    NASA Astrophysics Data System (ADS)

    Liu, Y.; McKinney, K. A.; Watson, T. B.; Springston, S. R.; Seco, R.; Park, J. H.; Kim, S.; Shilling, J. E.; Guenther, A. B.; Yee, L.; Isaacman-VanWertz, G. A.; Wernis, R. A.; Goldstein, A. H.; Brito, J.; Artaxo, P.; Souza, R. A. F. D.; Manzi, A. O.; Martin, S. T.

    2015-12-01

    Tropical rainforests are vigorous emitters of volatile organic compounds (VOCs) year round. Despite the small seasonal variation expected for tropical rainforests, converging evidence has shown that, among other factors, there can be considerable differences between the wet and dry seasons in leaf coverage, species composition, leaf-level photosynthetic photo flux, and ozone and NOx levels, which are important controlling factors of VOC emission and chemistry. There have been, however, a limited number of studies on the seasonality of VOC concentrations over tropical rainforests. As part of the GoAmazon 2014/5 Experiment, two-month continuous measurements of VOC compounds were carried out using a proton-transfer-reaction time-of-flight mass spectrometer (PTR-TOF-MS) at the T3 site in both the wet and dry seasons of 2014. During the dry season most biogenic VOC species and their oxidation products exhibited increased concentration. For some species, the diel pattern was also different between the two seasons. Implications of the seasonality of the emission and chemistry of biogenic VOCs, in particular isoprene and terpenes, are discussed.

  10. Influence of Oil and Gas Emissions on Ambient Atmospheric Volatile Organic Compounds in Residential Areas of Northeastern Colorado

    NASA Astrophysics Data System (ADS)

    Thompson, C. R.; Evans, J. M.; Wang, W.; Jacques, H.; Smith, K. R.; Terrell, R.; Helmig, D.

    2014-12-01

    The Northern Front Range (NFR) region of Colorado has experienced rapid expansion in drilling of shale and tight sands oil and gas reservoirs in recent years due to advances in hydraulic fracturing technology, with over 24,000 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 volatile organic compounds (VOC) for residents living near wells. Here we present observations of ambient atmospheric VOC present in residential areas located in close proximity to wells in Erie, Colorado, and show that 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. These data are combined with VOC observations from downtown Denver and Platteville, as well as with measurements conducted this summer in conjunction with the FRAPPE and DISCOVER-AQ flight campaigns, to investigate the spatial distribution of VOC enhancements in correlation with proximity to oil and gas production areas. We show that these compounds, including the BTEX aromatics, are elevated across the NFR, with highest levels in communities within the Greater Wattenberg Gas Field. These analyses demonstrate that VOC emissions from oil and gas operations represent a large area source for ozone precursors in the NFR.

  11. Volatile Organic Compounds Emissions from Luculia pinceana Flower and Its Changes at Different Stages of Flower Development.

    PubMed

    Li, Yuying; Ma, Hong; Wan, Youming; Li, Taiqiang; Liu, Xiuxian; Sun, Zhenghai; Li, Zhenghong

    2016-04-22

    Luculia plants are famed ornamental plants with sweetly fragrant flowers, of which L. pinceana Hooker, found primarily in Yunnan Province, China, has the widest distribution. Solid phase microextraction-gas chromatography-mass spectrometry (SPME-GC-MS) was employed to identify the volatile organic compounds (VOCs) emitted from different flower development stages of L. pinceana for the evaluation of floral volatile polymorphism. Peak areas were normalized as percentages and used to determine the relative amounts of the volatiles. The results showed that a total of 39 compounds were identified at four different stages of L. pinceana flower development, including 26 at the bud stage, 26 at the initial-flowering stage, 32 at the full-flowering stage, and 32 at the end-flowering stage. The most abundant compound was paeonol (51%-83%) followed by (E,E)-α-farnesene, cyclosativene, and δ-cadinene. All these volatile compounds create the unique fragrance of L. pinceana flower. Floral scent emission offered tendency of ascending first and descending in succession, meeting its peak level at the initial-flowering stage. The richest diversity of floral volatile was detected at the third and later periods of flower development. Principal component analysis (PCA) indicated that the composition and its relative content of floral scent differed throughout the whole flower development. The result has important implications for future floral fragrance breeding of Luculia. L. pinceana would be adequate for a beneficial houseplant and has a promising prospect for development as essential oil besides for a fragrant ornamental owing to the main compounds of floral scent with many medicinal properties.

  12. Geogenic and atmospheric sources for volatile organic compounds in fumarolic emissions from Mt. Etna and Vulcano Island (Sicily, Italy)

    NASA Astrophysics Data System (ADS)

    Tassi, F.; Capecchiacci, F.; Cabassi, J.; Calabrese, S.; Vaselli, O.; Rouwet, D.; Pecoraino, G.; Chiodini, G.

    2012-09-01

    In this paper, fluid source(s) and processes controlling the chemical composition of volatile organic compounds (VOCs) in gas discharges from Mt. Etna and Vulcano Island (Sicily, Italy) were investigated. The main composition of the Etnean and Volcano gas emissions is produced by mixing, to various degrees, of magmatic and hydrothermal components. VOCs are dominated by alkanes, alkenes and aromatics, with minor, though significant, concentrations of O-, S- and Cl(F)-substituted compounds. The main mechanism for the production of alkanes is likely related to pyrolysis of organic-matter-bearing sediments that interact with the ascending magmatic fluids. Alkanes are then converted to alkene and aromatic compounds via catalytic reactions (dehydrogenation and dehydroaromatization, respectively). Nevertheless, an abiogenic origin for the light hydrocarbons cannot be ruled out. Oxidative processes of hydrocarbons at relatively high temperatures and oxidizing conditions, typical of these volcanic-hydrothermal fluids, may explain the production of alcohols, esters, aldehydes, as well as O- and S-bearing heterocycles. By comparing the concentrations of hydrochlorofluorocarbons (HCFCs) in the fumarolic discharges with respect to those of background air, it is possible to highlight that they have a geogenic origin likely due to halogenation of both methane and alkenes. Finally, chlorofluorocarbon (CFC) abundances appear to be consistent with background air, although the strong air contamination that affects the Mt. Etna fumaroles may mask a possible geogenic contribution for these compounds. On the other hand, no CFCs were detected in the Vulcano gases, which are characterized by low air contribution. Nevertheless, a geogenic source for these compounds cannot be excluded on the basis of the present data.

  13. Trends in selected ambient volatile organic compound (VOC) concentrations and a comparison to mobile source emission trends in California's South Coast Air Basin

    NASA Astrophysics Data System (ADS)

    Pang, Yanbo; Fuentes, Mark; Rieger, Paul

    2015-12-01

    Trends in ambient concentrations of Volatile Organic Compounds (VOC) in the South Coast Air Basin (SoCAB) are compared to trends in VOC emissions from Light-Duty Gasoline Vehicles (LDGV) tested on chassis dynamometers and to trends observed in tunnel studies during the same period to understand the impacts of gasoline vehicle emissions on ambient VOC concentrations from 1999 to 2009. Annual median concentrations for most ambient VOCs decreased 40% from 1999 to 2009 in the SoCAB, based on data from the Photochemical Assessment Monitoring Stations (PAMS). Annual concentration decreases of most compounds, except 2,2,4-trimethylpentane, are highly correlated with the decrease of acetylene, a marker for tailpipe emissions from LDGV. This indicates that ambient VOC concentration decreases were likely due to tailpipe emission reductions from gasoline vehicles. Air Toxics Monitoring Network data also support this conclusion. Benzene concentration-normalized ratios for most compounds except ethane, propane, isoprene, and 2,2,4-trimethylpentane were stable even as these compound concentrations decreased significantly from 1999 to 2009. Such stability suggests that the main sources of ambient VOC were still the same from 1999 to 2009. The comparison of trends in dynamometer testing and tunnel studies also shows that tailpipe emissions remained the dominant source of tunnel LDGV emissions. The pronounced changes in 2,2,4-trimethylpentane ratios due to the introduction of Phase 3 gasoline also confirm the substantial impact of LDGV emissions on ambient VOCs. Diurnal ambient VOC data also suggest that LDGV tailpipe emissions remained the dominant source of ambient VOCs in the SoCAB in 2009. Our conclusion, which is that current inventory models underestimate VOC emissions from mobile sources, is consistent with that of several recent studies of ambient trends in the SoCAB. Our study showed that tailpipe emissions remained a bigger contributor to ambient VOCs than evaporative

  14. Chemical effects of CeL(gamma4) emission spectra for Ce compounds.

    PubMed

    Hayashi, Hisashi; Takehara, Yuki; Kawamura, Naomi; Mizumaki, Masaichiro

    2010-01-01

    High-resolution CeL(gamma4) emission spectra of CeF(3), Ce(2)S(3), CeF(4), and CeO(2) have been measured using a multicrystal, multidetector spectrometer. The spectra exhibited substantial differences depending on the chemical environment of the Ce ions. By comparing the observed CeO(2) spectrum with the band calculations, we determined that the observed chemical effects of the main emission line were primarily attributable to the transitions of the Ce5p band; the high-energy tail at around 6.539 keV was assigned to the ligand p-->Ce2s cross transition. Further, a key difference between CeL(gamma4) and EuL(gamma4) is discussed with reference to CeL(1)- and EuL(1)-X-ray absorption fine-structures (XAFS). Possible applications of CeL(gamma4) emissions to material characterization are also suggested.

  15. [Emission characteristics and hazard assessment analysis of volatile organic compounds from chemical synthesis pharmaceutical industry].

    PubMed

    Li, Yan; Wang, Zhe-Ming; Song, Shuang; Xu, Zhi-Rong; Xu, Ming-Zhu; Xu, Wei-Li

    2014-10-01

    In this study, volatile organic compounds (VOCs) released from chemical synthesis pharmaceutical industry in Taizhou, Zhejiang province were analyzed quantitatively and qualitatively. The total volatile organic compounds (TVOCs) was in the range of 14.9-308.6 mg · m(-3). Evaluation models of ozone formation potentials (OFP) and health risk assessment were adopted to preliminarily assess the environmental impact and health risk of VOCs. The results showed that the values of OFP of VOCs were in the range of 3.1-315.1 mg · m(-3), based on the maximum incremental reactivity, the main principal contribution was toluene, tetrahydrofuran (THF), acetic ether etc. The non-carcinogenic risk and the carcinogen risk fell in the ranges of 9.48 x 10(-7)-4.98 x 10(-4) a(-1) and 3.17 x 10(-5)- 6.33 x 10(-3). The principal contribution of VOCs was benzene, formaldehyde and methylene chloride.

  16. Historical gaseous and primary aerosol emissions in the United States from 1990 to 2010

    NASA Astrophysics Data System (ADS)

    Xing, J.; Pleim, J.; Mathur, R.; Pouliot, G.; Hogrefe, C.; Gan, C.-M.; Wei, C.

    2013-08-01

    An accurate description of emissions is crucial for model simulations to reproduce and interpret observed phenomena over extended time periods. In this study, we used an approach based on activity data to develop a consistent series of spatially resolved emissions in the United States from 1990 to 2010. The state-level anthropogenic emissions of SO2, NOx, CO, NMVOC (non-methane volatile organic compounds), NH3, PM10 and PM2.5 for a total of 49 sectors were estimated based on several long-term databases containing information about activities and emission controls. Activity data for energy-related stationary sources were derived from the State Energy Data System. Corresponding emission factors reflecting implemented emission controls were calculated back from the National Emissions Inventory (NEI) for seven years (i.e., 1990, 1995, 1996, 1999, 2001, 2002 and 2005), and constrained by the AP-42 (US EPA's Compilation of Air Pollutant Emissions Factors) dataset. Activity data for mobile sources including different types of highway vehicles and non-highway equipment were obtained from highway statistics reported by the Federal Highway Administration. The trends in emission factors for highway mobile source were informed by the 2011 National Transportation Statistics. Emissions for all non-energy-related sources were either scaled by the growth ratio of activity indicators or adjusted based on the NEI trends report. Because of the strengthened control efforts, particularly for the power sector and mobile sources, emissions of all pollutants except NH3 were reduced by half over the last two decades. The emission trends developed in this study are comparable with the NEI trend report and EDGAR (Emissions Database for Global Atmospheric Research) data, but better constrained by trends in activity data. Reductions in SO2, NOx, CO and EC (speciation of PM2.5 by SMOKE, Sparse Matrix Operator Kernel Emissions) emissions agree well with the observed changes in ambient SO2, NO2

  17. Particulate Matter Sampling and Volatile Organic Compound Removal for Characterization of Spark Ignited Direct Injection Engine Emissions

    SciTech Connect

    Matthias, Nicholas; Farron, Carolyn; Foster, David E.; Andrie, Michael; Krieger, Roger; Najt, Paul; Narayanaswamy, Kushal; Solomon, Arun; Zelenyuk, Alla

    2011-08-30

    More stringent emissions regulations are continually being proposed to mitigate adverse human health and environmental impacts of internal combustion engines. With that in mind, it has been proposed that vehicular particulate matter (PM) emissions should be regulated based on particle number in addition to particle mass. One aspect of this project is to study different sample handling methods for number based aerosol measurements, specifically, two different methods for removing volatile organic compounds (VOCs). One method is a thermodenuder (TD) and the other is an evaporative chamber/diluter (EvCh). These sample handling methods have been implemented in an engine test cell with a spark ignited direct injection (SIDI) engine. The engine was designed for stoichiometric, homogeneous combustion. SIDI is of particular interest for improved fuel efficiency compared to other SI engines, however, the efficiency benefit comes with greater PM emissions and may therefore be subject to the proposed number based PM regulation. Another aspect of this project is to characterize PM from this engine in terms of particle number and composition

  18. Particulate Matter Sampling and Volatile Organic Compound Removal for Characterization of Spark Ignited Direct Injection Engine Emissions

    SciTech Connect

    Matthias, Nicholas; Farron, Carrie; Foster, David E.; Andrie, Michael; Krieger, Roger; Najt, Paul M.; Narayanaswamy, Kushal; Solomon, Arun S.; Zelenyuk, Alla

    2012-01-01

    More stringent emissions regulations are continually being proposed to mitigate adverse human health and environmental impacts of internal combustion engines. With that in mind, it has been proposed that vehicular particulate matter (PM) emissions should be regulated based on particle number in addition to particle mass. One aspect of this project is to study different sample handling methods for number based aerosol measurements, specifically, two different methods for removing volatile organic compounds (VOCs). One method is a thermodenuder (TD) and the other is an evaporative chamber/diluter (EvCh). These sample handling methods have been implemented in an engine test cell with a spark ignited direct injection (SIDI) engine. The engine was designed for stoichiometric, homogeneous combustion. SIDI is of particular interest for improved fuel efficiency compared to other SI engines, however, the efficiency benefit comes with greater PM emissions and may therefore be subject to the proposed number based PM regulation. Another aspect of this project is to characterize PM from this engine in terms of particle number and composition.

  19. Volatile Organic Compound and Particulate Emission Studies of AF (Air Force) Paint Booth Facilities. Phase 1.

    DTIC Science & Technology

    1988-07-01

    Schaums outline series, McGraw Hill Book Company, September 1986. 13. Rule 451; Surface Coatings of Miscellaneous Metal Parts and Products. Sacramento...analyzed as soon as possible by the Acurex Chemistry Laboratory. The accuracy and completeness of each data set were determined based on the quality...compounds of interest. Three sets of tubes were submitted for analysis to the Acurex Chemistry Laboratory, thus three clean tubes were spiked with tne

  20. Anthropogenic emissions in Nigeria and implications for atmospheric ozone pollution: A view from space

    NASA Astrophysics Data System (ADS)

    Marais, E. A.; Jacob, D. J.; Wecht, K.; Lerot, C.; Zhang, L.; Yu, K.; Kurosu, T. P.; Chance, K.; Sauvage, B.

    2014-12-01

    Nigeria has a high population density and large fossil fuel resources but very poorly managed energy infrastructure. Satellite observations of formaldehyde (HCHO) and glyoxal (CHOCHO) reveal very large sources of anthropogenic nonmethane volatile organic compounds (NMVOCs) from the Lagos megacity and oil/gas operations in the Niger Delta. This is supported by aircraft observations over Lagos and satellite observations of methane in the Niger Delta. Satellite observations of carbon monoxide (CO) and nitrogen dioxide (NO2) show large seasonal emissions from open fires in December-February (DJF). Ventilation of central Nigeria is severely restricted at that time of year, leading to very poor ozone air quality as observed from aircraft (MOZAIC) and satellite (TES). Simulations with the GEOS-Chem chemical transport model (CTM) suggest that maximum daily 8-h average (MDA8) ozone exceeds 70 ppbv over the region on a seasonal mean basis, with significant contributions from both open fires (15-20 ppbv) and fuel/industrial emissions (7-9 ppbv). The already severe ozone pollution in Nigeria could worsen in the future as a result of demographic and economic growth, although this would be offset by a decrease in open fires.

  1. Emissions of biogenic volatile organic compounds and subsequent formation of secondary organic aerosols in a Larix kaempferi forest

    NASA Astrophysics Data System (ADS)

    Mochizuki, T.; Miyazaki, Y.; Ono, K.; Wada, R.; Takahashi, Y.; Saigusa, N.; Kawamura, K.; Tani, A.

    2015-04-01

    We conducted simultaneous measurements of concentrations and above-canopy fluxes of isoprene and α-pinene, along with their oxidation products in aerosols in a Larix kaempferi (Japanese larch) forest in summer 2012. Vertical profiles of isoprene showed the maximum concentration near the forest floor with a peak around noon, whereas oxidation products of isoprene, i.e., methacrolein (MACR) and methyl vinyl ketone (MVK), showed higher concentrations near the canopy level of the forest. The vertical profile suggests large emissions of isoprene near the forest floor, likely due to Dryopteris crassirhizoma (a fern species), and the subsequent reaction within the canopy. The concentrations of α-pinene also showed highest values near the forest floor with maximums in the early morning and late afternoon. The vertical profiles of α-pinene suggest its large emissions from soil and litter in addition to emissions from L. kaempferi leaves at the forest site. Isoprene and its oxidation products in aerosols exhibited similar diurnal variations within the forest canopy, providing evidence for secondary organic aerosol (SOA) formation via oxidation of isoprene most likely emitted from the forest floor. Although high abundance of α-pinene was observed in the morning, its oxidation products in aerosols showed peaks in daytime, due to a time lag between the emission and atmospheric reactions of α-pinene to form SOA. Positive matrix factorization (PMF) analysis indicated that anthropogenic influence is the most important factor contributing to the elevated concentrations of molecular oxidation products of isoprene- (> 64%) and α-pinene-derived SOA (> 57%). The combination of the measured fluxes and vertical profiles of biogenic volatile organic compounds (BVOCs) suggests that the inflow of anthropogenic precursors/aerosols likely enhanced the formation of both isoprene- and α-pinene-SOA within the forest canopy even when the BVOC flux was relatively low. This study highlights

  2. Carbonyl compounds emitted by a diesel engine fuelled with diesel and biodiesel-diesel blends: Sampling optimization and emissions profile

    NASA Astrophysics Data System (ADS)

    Guarieiro, Lílian Lefol Nani; Pereira, Pedro Afonso de Paula; Torres, Ednildo Andrade; da Rocha, Gisele Olimpio; de Andrade, Jailson B.

    Biodiesel is emerging as a renewable fuel, hence becoming a promising alternative to fossil fuels. Biodiesel can form blends with diesel in any ratio, and thus could replace partially, or even totally, diesel fuel in diesel engines what would bring a number of environmental, economical and social advantages. Although a number of studies are available on regulated substances, there is a gap of studies on unregulated substances, such as carbonyl compounds, emitted during the combustion of biodiesel, biodiesel-diesel and/or ethanol-biodiesel-diesel blends. CC is a class of hazardous pollutants known to be participating in photochemical smog formation. In this work a comparison was carried out between the two most widely used CC collection methods: C18 cartridges coated with an acid solution of 2,4-dinitrophenylhydrazine (2,4-DNPH) and impinger bottles filled in 2,4-DNPH solution. Sampling optimization was performed using a 2 2 factorial design tool. Samples were collected from the exhaust emissions of a diesel engine with biodiesel and operated by a steady-state dynamometer. In the central body of factorial design, the average of the sum of CC concentrations collected using impingers was 33.2 ppmV but it was only 6.5 ppmV for C18 cartridges. In addition, the relative standard deviation (RSD) was 4% for impingers and 37% for C18 cartridges. Clearly, the impinger system is able to collect CC more efficiently, with lower error than the C18 cartridge system. Furthermore, propionaldehyde was nearly not sampled by C18 system at all. For these reasons, the impinger system was chosen in our study. The optimized sampling conditions applied throughout this study were: two serially connected impingers each containing 10 mL of 2,4-DNPH solution at a flow rate of 0.2 L min -1 during 5 min. A profile study of the C1-C4 vapor-phase carbonyl compound emissions was obtained from exhaust of pure diesel (B0), pure biodiesel (B100) and biodiesel-diesel mixtures (B2, B5, B10, B20, B50, B

  3. Performance of a pilot-scale biotrickling filter in controlling the volatile organic compound emissions in a furniture manufacturing facility.

    PubMed

    Martínez-Soria, Vicente; Gabaldón, Carmen; Penya-Roja, Josep M; Palau, Jordi; Alvarez-Hornos, F Javier; Sempere, Feliu; Soriano, Carlos

    2009-08-01

    A 0.75-m3 pilot-scale biotrickling filter was run for over 1 yr in a Spanish furniture company to evaluate its performance in the removal of volatile organic compounds (VOCs) contained in the emission of two different paint spray booths. The first one was an open front booth used to manually paint furniture, and the second focus was an automatically operated closed booth operated to paint pieces of furniture. In both cases, the VOC emissions were very irregular, with rapid and extreme fluctuations. The pilot plant was operated at an empty bed residence time (EBRT) ranging from 10 to 40 sec, and good removal efficiencies of VOCs were usually obtained. When a buffering activated carbon prefilter was installed, the system performance was improved considerably, so a much better compliance with legal constraints was reached. After different shutdowns in the factory, the period to recover the previous performance of the biotrickling reactor was minimal. A weekend dehydration strategy was developed and implemented to control the pressure drop associated with excessive biomass accumulation.

  4. Emissions of Ultrafine Particles and Volatile Organic Compounds from Commercially Available Desktop Three-Dimensional Printers with Multiple Filaments.

    PubMed

    Azimi, Parham; Zhao, Dan; Pouzet, Claire; Crain, Neil E; Stephens, Brent

    2016-02-02

    Previous research has shown that desktop 3D printers can emit large numbers of ultrafine particles (UFPs, particles less than 100 nm) and some hazardous volatile organic compounds (VOCs) during printing, although very few filament and 3D printer combinations have been tested to date. Here we quantify emissions of UFPs and speciated VOCs from five commercially available filament extrusion desktop 3D printers utilizing up to nine different filaments by controlled experiments in a test chamber. Median estimates of time-varying UFP emission rates ranged from ∼10(8) to ∼10(11) min(-1) across all tested combinations, varying primarily by filament material and, to a lesser extent, bed temperature. The individual VOCs emitted in the largest quantities included caprolactam from nylon-based and imitation wood and brick filaments (ranging from ∼2 to ∼180 μg/min), styrene from acrylonitrile butadiene styrene (ABS) and high-impact polystyrene (HIPS) filaments (ranging from ∼10 to ∼110 μg/min), and lactide from polylactic acid (PLA) filaments (ranging from ∼4 to ∼5 μg/min). Results from a screening analysis of potential exposure to these products in a typical small office environment suggest caution should be used when operating many of the printer and filament combinations in poorly ventilated spaces or without the aid of combined gas and particle filtration systems.

  5. Solvatochromism, Reversible Chromism and Self-Assembly Effects of Heteroatom-Assisted Aggregation-Induced Enhanced Emission (AIEE) Compounds.

    PubMed

    Niu, Caixia; You, Ying; Zhao, Liu; He, Dacheng; Na, Na; Ouyang, Jin

    2015-09-28

    Two compounds, 9,10-bis[2-(quinolyl)vinyl]anthracene (BQVA) and 9,10-bis[2-(naphthalen-2-yl)vinyl]anthracene (BNVA), have been synthesised and investigated. Both of them have aggregation-induced enhanced emission (AIEE) properties. Heteroatom-assisted BQVA shows solvatochromism, reversible chromism properties and self-assembly effects. When increasing the solvent polarities, the green solution of BQVA turns to orange with a redshift of the fluorescence emission wavelengths from λ=527 to 565 nm. Notably, BQVA exhibits reversible chromism properties, including mechano- and thermochromism. The as-prepared BQVA powders show green fluorescence (λem=525 nm) and the colour can turn into orange (λem=573 nm) after grinding. Interestingly, the orange colour can return at high temperature. Based on these reversible chromism properties, a simple and convenient erasable board has been designed. Different from BQVA, non-heteroatom-assisted BNVA has no clear chromic processes. The results obtained from XRD, differential scanning calorimetry, single-crystal analysis and theoretical calculations indicate that the chromic processes depend on the heteroatoms in BQVA. Additionally, BQVA also exhibits excellent self-assembly effects in different solvents. Homogeneous nanospheres are formed in mixtures of tetrahydrofuran and water, which are then doped into silica nanoparticles and treated with 3-aminopropyltriethoxysilane to give amino-functionalised nanoparticles (BQVA-AFNPs). The BQVAAFNPs could be used to stain protein markers in polyacrylamide gel electrophoresis.

  6. Development and Application of a Fast Chromatography Technique for Analysis of Biogenic Volatile Organic Compounds in Plant Emissions

    NASA Astrophysics Data System (ADS)

    Jones, C. E.; Kato, S.; Nakashima, Y.; Yamazakii, S.; Kajii, Y. J.

    2011-12-01

    Biogenic volatile organic compounds (BVOCs) emitted from vegetation constitute the largest fraction (>90 %) of total global non-methane VOC supplied to the atmosphere, yet the chemical complexity of these emissions means that achieving comprehensive measurements of BVOCs, and in particular the less volatile terpenes, is not straightforward. As such, there is still significant uncertainty associated with the contribution of BVOCs to the tropospheric oxidation budget, and to atmospheric secondary organic aerosol (SOA) formation. The rate of BVOC emission from vegetation is regulated by environmental conditions such as light intensity and temperature, and thus can be highly variable, necessitating high time-resolution BVOC measurements. In addition, the numerous monoterpene and sesquiterpene isomers, which are indistinguishable by some analytical techniques, have greatly varying lifetimes with respect to atmospheric oxidants, and as such quantification of each individual isomer is fundamental to achieving a comprehensive characterisation of the impact of BVOCs upon the atmospheric oxidation capacity. However, established measurement techniques for these trace gases typically offer a trade-off between sample frequency and the level of speciation; detailed information regarding chemical composition may be obtained, but with reduced time resolution, or vice versa. We have developed a Fast-GC-FID technique for quantification of a range of monoterpene, sesquiterpene and oxygenated C10 BVOC isomers, which retains the separation capability of conventional gas chromatography, yet offers considerably improved sample frequency. Development of this system is ongoing, but currently a 20 m x 0.18 mm i.d resistively heated metal column is employed to achieve chromatographic separation of thirteen C10-C15 BVOCs, within a total cycle time of ~15 minutes. We present the instrument specifications and analytical capability, together with the first application of this Fast-GC technique

  7. Measurements of Volatile Organic Compounds (VOCs) from Biomass Combustion - Emission Ratios, OH Reactivities and SOA Precursors

    NASA Astrophysics Data System (ADS)

    Kuster, W. C.; Gilman, J. B.; Goldan, P. D.; Warneke, C.; Degouw, J.; Veres, P. R.; Burling, I. R.; Yokelson, R. J.

    2009-12-01

    Multiple instruments including a gas chromatograph/mass spectrometer (GC/MS), a proton transfer reaction mass spectrometer (PTR-MS), a proton ion trap mass spectrometer (PIT-MS), a negative-ion proton-transfer chemical-ionization mass spectrometer (NI-PT-CIMS) and a Fourier-transform infrared spectrometer (FTIR) acquired data from 77 burns of various biomass fuels conducted at the U.S. Department of Agriculture (USDA) Forest Sciences Laboratory (FSL) in Missoula, MT in February 2009. We compare VOC measurements of oxygenates, aromatics and biogenics from the various instruments as well as from the various fuel types collected in southeastern and southwestern regions of the United States. The relative contribution of the combustion species to the total reactivity with the OH radical is calculated and compared to ambient air reactivity in various locations. Total reactivity for measured species in these fires occasionally exceeded 1000 sec-1 with the majority of this reactivity due to alkenes. In addition, we investigate the relative contribution of the combustion species to the potential for secondary organic aerosol (SOA) formation. Measurements of several compounds not previously reported in various urban ambient air measurement campaigns such as pyrazole (C3H4N2), pyrrole (C4H5N), benzofuran (C8H6O) and 2-furanaldehyde (C5H4O2), which are highly reactive with OH, will be presented.

  8. Characterization of Volatile Organic Compound (VOC) Emissions at Sites of Oil Sands Extraction and Upgrading in northern Alberta

    NASA Astrophysics Data System (ADS)

    Marrero, J.; Simpson, I. J.; Meinardi, S.; Blake, D. R.

    2011-12-01

    The crude oil reserves in Canada's oil sands are second only to Saudi Arabia, holding roughly 173 billion barrels of oil in the form of bitumen, an unconventional crude oil which does not flow and cannot be pumped without heating or dilution. Oil sands deposits are ultimately used to make the same petroleum products as conventional forms of crude oil, though more processing is required. Hydrocarbons are the basis of oil, coal and natural gas and are an important class of gases emitted into the atmosphere during oil production, particularly because of their effects on air quality and human health. However, they have only recently begun to be independently assessed in the oil sands regions. As part of the 2008 ARCTAS airborne mission, whole air samples were collected in the boundary layer above the surface mining operations of northern Alberta. Gas chromatography analysis revealed enhanced concentrations of 53 VOCs (C2 to C10) over the mining region. When compared to local background levels, the measured concentrations were enhanced up to 1.1-400 times for these compounds. To more fully characterize emissions, ground-based studies were conducted in summer 2010 and winter 2011 in the oil sands mining and upgrading areas. The data from the 200 ground-based samples revealed enhancements in the concentration of 65 VOCs. These compounds were elevated up to 1.1-3000 times above background concentrations and include C2-C8 alkanes, C1-C5 alkyl nitrates, C2-C4 alkenes and potentially toxic aromatic compounds such as benzene, toluene, and xylenes.

  9. PAH, BTEX, carbonyl compound, black-carbon, NO2 and ultrafine particle dynamometer bench emissions for Euro 4 and Euro 5 diesel and gasoline passenger cars

    NASA Astrophysics Data System (ADS)

    Louis, Cédric; Liu, Yao; Tassel, Patrick; Perret, Pascal; Chaumond, Agnès; André, Michel

    2016-09-01

    Although implementing Diesel particulate filters (DPF) and other novel aftertreatment technologies makes it possible to achieve significant reductions in particle mass emissions, it may induce the release of ultrafine particles and emissions of many other unregulated compounds. This paper focuses on (i) ultrafine particles, black carbon, BTEX, PAH, carbonyl compounds, and NO2 emissions from Euro 4 and Euro 5 Diesel and gasoline passenger cars, (ii) the influence of driving conditions (e.g., cold start, urban, rural and motorway conditions), and (iii) the impact of additive and catalysed DPF devices on vehicle emissions. Chassis dynamometer tests were conducted on four Euro 5 vehicles and two Euro 4 vehicles: gasoline vehicles with and without direct injection system and Diesel vehicles equipped with additive and catalysed particulate filters. The results showed that compared to hot-start cycles, cold-start urban cycles increased all pollutant emissions by a factor of two. The sole exception was NO2, which was reduced by a factor of 1.3-6. Particulate and black carbon emissions from the gasoline engines were significantly higher than those from the Diesel engines equipped with DPF. Moreover, the catalysed DPF emitted about 3-10 times more carbonyl compounds and particles than additive DPF, respectively, during urban driving cycles, while the additive DPF vehicles emitted 2 and 5 times more BTEX and carbonyl compounds during motorway driving cycles. Regarding particle number distribution, the motorway driving cycle induced the emission of particles smaller in diameter (mode at 15 nm) than the urban cold-start cycle (mode at 80-100 nm). The results showed a clear positive correlation between particle, black carbon, and BTEX emissions, and a negative correlation between particles and NO2.

  10. Response of lightning NOx emissions and ozone production to climate change: Insights from the Atmospheric Chemistry and Climate Model Intercomparison Project

    NASA Astrophysics Data System (ADS)

    Finney, D. L.; Doherty, R. M.; Wild, O.; Young, P. J.; Butler, A.

    2016-05-01

    Results from an ensemble of models are used to investigate the response of lightning nitrogen oxide emissions to climate change and the consequent impacts on ozone production. Most models generate lightning using a parameterization based on cloud top height. With this approach and a present-day global emission of 5 TgN, we estimate a linear response with respect to changes in global surface temperature of +0.44 ± 0.05 TgN K-1. However, two models using alternative approaches give +0.14 and -0.55 TgN K-1 suggesting that the simulated response is highly dependent on lightning parameterization. Lightning NOx is found to have an ozone production efficiency of 6.5 ± 4.7 times that of surface NOx sources. This wide range of efficiencies across models is partly due to the assumed vertical distribution of the lightning source and partly to the treatment of nonmethane volatile organic compound (NMVOC) chemistry. Careful consideration of the vertical distribution of emissions is needed, given its large influence on ozone production.

  11. Insect herbivore feeding and their excretion contribute to volatile organic compounds emission to the atmosphere

    NASA Astrophysics Data System (ADS)

    Zebelo, S.; Gnavi, G.; Bertea, C.; Bossi, S.; Andrea, O.; Cordero, C.; Rubiolo, P.; Bicchi, C.; Maffei, M.

    2011-12-01

    Secondary plant metabolites play an important role in insect plant interactions. The Lamiaceae family, especially Mentha species, accumulate secondary plant metabolites in their glandular trichomes, mainly mono and sesquiterpenes. Here we show that mint plants respond to herbivory by changing the quality and quantity of leaf secondary plant metabolite components. The volatiles from herbivore damaged, mechanical damage and healthy plant were collected by HS-SPME and analyzed by GC-MS. Plants with the same treatment were kept for genomic analysis. Total RNA was extracted from the above specified treatments. The terpenoid quantitative gene expressions (qPCR) were then assayed. Upon herbivory, M. aquatica synthesizes and emits (+)-menthofuran and the other major monoterpene (+)-pulegone emitted by healthy and mechanically damaged plants. Herbivory was found to up-regulate the expression of genes involved in terpenoid biosynthesis. The increased emission of (+)-menthofuran was correlated with the upregulation of (+)-menthofuran synthase. In addition we analysed the VOC composition of C. herbacea frass from insects feeding on Mentha aquatica. VOCs were sampled by HS-SPME and analyzed by GCxGC-qMS, and the results compared through quantitative comparative analysis of 2D chromatographic data. Most terpenoids from M. aquatica were completely catabolized by C. herbacea and were absent in the frass volatile fraction. On the other hand, the monoterpene 1,8-cineole was oxidized and frass yielded several new hydroxy-1,8-cineoles, among which 2α-OH-, 3α-OH-, 3β-OH- and 9-OH-1,8-cineole. The role of VOC emitted during herbivory and frass excretion on secondary organic aerosol formation is discussed.

  12. Differential controls by climate and physiology over the emission rates of biogenic volatile organic compounds from mature trees in a semi-arid pine forest.

    PubMed

    Eller, Allyson S D; Young, Lindsay L; Trowbridge, Amy M; Monson, Russell K

    2016-02-01

    Drought has the potential to influence the emission of biogenic volatile organic compounds (BVOCs) from forests and thus affect the oxidative capacity of the atmosphere. Our understanding of these influences is limited, in part, by a lack of field observations on mature trees and the small number of BVOCs monitored. We studied 50- to 60-year-old Pinus ponderosa trees in a semi-arid forest that experience early summer drought followed by late-summer monsoon rains, and observed emissions for five BVOCs-monoterpenes, methylbutenol, methanol, acetaldehyde and acetone. We also constructed a throughfall-interception experiment to create "wetter" and "drier" plots. Generally, trees in drier plots exhibited reduced sap flow, photosynthesis, and stomatal conductances, while BVOC emission rates were unaffected by the artificial drought treatments. During the natural, early summer drought, a physiological threshold appeared to be crossed when photosynthesis ≅2 μmol m(-2) s(-1) and conductance ≅0.02 mol m(-2) s(-1). Below this threshold, BVOC emissions are correlated with leaf physiology (photosynthesis and conductance) while BVOC emissions are not correlated with other physicochemical factors (e.g., compound volatility and tissue BVOC concentration) that have been shown in past studies to influence emissions. The proportional loss of C to BVOC emission was highest during the drought primarily due to reduced CO2 assimilation. It appears that seasonal drought changes the relations among BVOC emissions, photosynthesis and conductance. When drought is relaxed, BVOC emission rates are explained mostly by seasonal temperature, but when seasonal drought is maximal, photosynthesis and conductance-the physiological processes which best explain BVOC emission rates-decline, possibly indicating a more direct role of physiology in controlling BVOC emission.

  13. Emissions of biogenic volatile organic compounds and subsequent formation of secondary organic aerosols in a Larix kaempferi forest

    NASA Astrophysics Data System (ADS)

    Mochizuki, T.; Miyazaki, Y.; Ono, K.; Wada, R.; Takahashi, Y.; Saigusa, N.; Kawamura, K.; Tani, A.

    2015-10-01

    We conducted simultaneous measurements of concentrations and above-canopy fluxes of isoprene and α-pinene, along with their oxidation products in aerosols in a Larix kaempferi (Japanese larch) forest in summer 2012. Vertical profiles of isoprene showed the maximum concentration near the forest floor with a peak around noon, whereas oxidation products of isoprene, i.e., methacrolein (MACR) and methyl vinyl ketone (MVK), showed higher concentrations near the canopy level of the forest. The vertical profile suggests large emissions of isoprene near the forest floor, likely due to Dryopteris crassirhizoma (a fern species), and the subsequent reaction within the canopy. The concentrations of α-pinene also showed highest values near the forest floor, with maximums in the early morning and late afternoon. The vertical profiles of α-pinene suggest its large emissions from soil and litter in addition to emissions from L. kaempferi leaves at the forest site. Isoprene and its oxidation products in aerosols exhibited similar diurnal variations within the forest canopy, providing evidence of secondary organic aerosol (SOA) formation via oxidation of isoprene most likely emitted from the forest floor. Although high abundance of α-pinene was observed in the morning, its oxidation products in aerosols showed peaks in daytime, due to a time lag between the emission and atmospheric reactions of α-pinene to form SOA. Positive matrix factorization (PMF) analysis indicated that anthropogenic influence is the most important factor contributing to the elevated concentrations of molecular oxidation products of isoprene- (> 64 %) and α-pinene-derived SOA (> 57 %). The combination of the measured fluxes and vertical profiles of biogenic volatile organic compounds (BVOCs) suggests that the inflow of anthropogenic precursors/aerosols likely enhanced the formation of both isoprene SOA and α-pinene SOA within the forest canopy even when the BVOC flux was relatively low. This study

  14. Emissions of terpenoids, benzenoids, and other biogenic gas-phase organic compounds from agricultural crops and their potential implications for air quality

    NASA Astrophysics Data System (ADS)

    Gentner, D. R.; Ormeño, E.; Fares, S.; Ford, T. B.; Weber, R.; Park, J.-H.; Brioude, J.; Angevine, W. M.; Karlik, J. F.; Goldstein, A. H.

    2014-06-01

    Agriculture comprises a substantial, and increasing, fraction of land use in many regions of the world. Emissions from agricultural vegetation and other biogenic and anthropogenic sources react in the atmosphere to produce ozone and secondary organic aerosol, which comprises a substantial fraction of particulate matter (PM2.5). Using data from three measurement campaigns, we examine the magnitude and composition of reactive gas-phase organic carbon emissions from agricultural crops and their potential to impact regional air quality relative to anthropogenic emissions from motor vehicles in California's San Joaquin Valley, which is out of compliance with state and federal standards for tropospheric ozone PM2.5. Emission rates for a suite of terpenoid compounds were measured in a greenhouse for 25 representative crops from California in 2008. Ambient measurements of terpenoids and other biogenic compounds in the volatile and intermediate-volatility organic compound ranges were made in the urban area of Bakersfield and over an orange orchard in a rural area of the San Joaquin Valley during two 2010 seasons: summer and spring flowering. We combined measurements from the orchard site with ozone modeling methods to assess the net effect of the orange trees on regional ozone. When accounting for both emissions of reactive precursors and the deposition of ozone to the orchard, the orange trees are a net source of ozone in the springtime during flowering, and relatively neutral for most of the summer until the fall, when it becomes a sink. Flowering was a major emission event and caused a large increase in emissions including a suite of compounds that had not been measured in the atmosphere before. Such biogenic emission events need to be better parameterized in models as they have significant potential to impact regional air quality since emissions increase by several factors to over an order of magnitude. In regions like the San Joaquin Valley, the mass of biogenic

  15. CAIRPOL CAIRCLIP NM-VOC

    EPA Science Inventory

    The CairPol CairClip O3-NO2 is a lightweight, portable sensor for measuring ozone (O3) and nitrogen dioxide (NO2) in parts per billion (ppb) or micrograms per cubic meter (µg/m3) in applications such as personal exposure and indoor and outdoor air quality monitoring. It uses a mi...

  16. Effect of biogenic volatile organic compound emissions on tropospheric chemistry during the Atmospheric Pollution Over the Paris Area (ESQUIF) campaign in the Ile-de-France region

    NASA Astrophysics Data System (ADS)

    Derognat, C.; Beekmann, M.; Baeumle, M.; Martin, D.; Schmidt, H.

    2003-09-01

    This paper investigates the impact of biogenic isoprene and terpene emissions on photochemical species levels in the French Ile-de-France region during several photooxidant pollution episodes in summer 1998 and 1999 during the Atmospheric Pollution Over the Paris Area (ESQUIF) project. The effect of biogenic emissions on both ozone produced on a continental scale and advected in Ile-de-France and on ozone locally formed are assessed. For this purpose, simulations with and without biogenic emissions are performed with a nested version of the CHIMERE model. This chemistry transport model includes both a continental (western European) domain with 0.5° horizontal resolution and a regional domain (Ile-de-France) of 150 × 150 km extension with a horizontal resolution of 6 km. An emissions database for biogenic isoprene and terpene emissions from forests has been set up. These emissions are estimated using emission factors for different tree species recently revised by [1999] and for different land use data sets, including highly resolved (1 km) satellite measurements for Ile-de-France. Good agreement has been found between modeled and measured (by aircraft) isoprene levels (overall bias <10%), which lends confidence to the use of the emissions database for subsequent simulations. The comparison between runs with and without biogenic volatile organic compound (VOC) emissions indicates a significant difference in ozone in Ile-de-France, up to 40 ppb for one extreme day. Biogenic VOC emissions from Ile-de-France along with those from outside the Ile-de-France region have an approximately equal responsibility for the additional ozone buildup. The main reason for this increased ozone formation is the enhancement of radicals due to larger concentrations of carbonyl species and ozone and their subsequent photolysis. Biogenic emissions lead to a shift in the sensitivity to emissions (toward more "NOx-limited"). However, generally, either with or without biogenic emissions, a

  17. Diel Variation of Biogenic Volatile Organic Compound Emissions- A field Study in the Sub, Low and High Arctic on the Effect of Temperature and Light

    PubMed Central

    Lindwall, Frida; Faubert, Patrick; Rinnan, Riikka

    2015-01-01

    Many hours of sunlight in the midnight sun period suggest that significant amounts of biogenic volatile organic compounds (BVOCs) may be released from arctic ecosystems during night-time. However, the emissions from these ecosystems are rarely studied and limited to point measurements during daytime. We measured BVOC emissions during 24-hour periods in the field using a push-pull chamber technique and collection of volatiles in adsorbent cartridges followed by analysis with gas chromatography- mass spectrometry. Five different arctic vegetation communities were examined: high arctic heaths dominated by Salix arctica and Cassiope tetragona, low arctic heaths dominated by Salix glauca and Betula nana and a subarctic peatland dominated by the moss Warnstorfia exannulata and the sedge Eriophorum russeolum. We also addressed how climate warming affects the 24-hour emission and how the daytime emissions respond to sudden darkness. The emissions from the high arctic sites were lowest and had a strong diel variation with almost no emissions during night-time. The low arctic sites as well as the subarctic site had a more stable release of BVOCs during the 24-hour period with night-time emissions in the same range as those during the day. These results warn against overlooking the night period when considering arctic emissions. During the day, the quantity of BVOCs and the number of different compounds emitted was higher under ambient light than in darkness. The monoterpenes α-fenchene, α -phellandrene, 3-carene and α-terpinene as well as isoprene were absent in dark measurements during the day. Warming by open top chambers increased the emission rates both in the high and low arctic sites, forewarning higher emissions in a future warmer climate in the Arctic. PMID:25897519

  18. Diel Variation of Biogenic Volatile Organic Compound Emissions--A field Study in the Sub, Low and High Arctic on the Effect of Temperature and Light.

    PubMed

    Lindwall, Frida; Faubert, Patrick; Rinnan, Riikka

    2015-01-01

    Many hours of sunlight in the midnight sun period suggest that significant amounts of biogenic volatile organic compounds (BVOCs) may be released from arctic ecosystems during night-time. However, the emissions from these ecosystems are rarely studied and limited to point measurements during daytime. We measured BVOC emissions during 24-hour periods in the field using a push-pull chamber technique and collection of volatiles in adsorbent cartridges followed by analysis with gas chromatography-mass spectrometry. Five different arctic vegetation communities were examined: high arctic heaths dominated by Salix arctica and Cassiope tetragona, low arctic heaths dominated by Salix glauca and Betula nana and a subarctic peatland dominated by the moss Warnstorfia exannulata and the sedge Eriophorum russeolum. We also addressed how climate warming affects the 24-hour emission and how the daytime emissions respond to sudden darkness. The emissions from the high arctic sites were lowest and had a strong diel variation with almost no emissions during night-time. The low arctic sites as well as the subarctic site had a more stable release of BVOCs during the 24-hour period with night-time emissions in the same range as those during the day. These results warn against overlooking the night period when considering arctic emissions. During the day, the quantity of BVOCs and the number of different compounds emitted was higher under ambient light than in darkness. The monoterpenes α-fenchene, α-phellandrene, 3-carene and α-terpinene as well as isoprene were absent in dark measurements during the day. Warming by open top chambers increased the emission rates both in the high and low arctic sites, forewarning higher emissions in a future warmer climate in the Arctic.

  19. Biogenic volatile organic compound emissions during BEARPEX 2009 measured by eddy covariance and flux-gradient similarity methods

    NASA Astrophysics Data System (ADS)

    Park, J.-H.; Fares, S.; Weber, R.; Goldstein, A. H.

    2014-01-01

    The Biosphere Effects on AeRosols and Photochemistry EXperiment (BEARPEX) took place in Blodgett Forest, a Ponderosa pine forest in the Sierra Nevada of California, USA, during summer 2009. We deployed a proton transfer reaction-quadrupole mass spectrometer (PTR-QMS) to measure fluxes and concentrations of biogenic volatile organic compounds (BVOCs). Eighteen ion species, including the major BVOC expected at the site, were measured sequentially at 5 heights to observe their vertical gradient from the forest floor to above the canopy. Fluxes of the 3 dominant BVOCs methanol, 2-Methyl-3-butene-2-ol (MBO), and monoterpenes were measured above the canopy by the disjunct eddy covariance (EC) method. Canopy-scale fluxes were also determined by the flux-gradient similarity method (K-theory). A universal K (Kuniv) was determined as the mean of individual K's calculated from the measured fluxes divided by vertical gradients for methanol, MBO, and monoterpenes. This Kuniv was then multiplied by the gradients of each observed ion species to compute their fluxes. The flux-gradient similarity method showed very good agreement with the disjunct EC method. Fluxes are presented for all measured species and compared to historical measurements from the same site, and used to test emission algorithms used to model fluxes at the regional scale. MBO was the dominant emission observed, followed by methanol, monoterpenes, acetone, and acetaldehyde. The flux-gradient similarity method is shown to be tenable, and we recommend its use, especially in experimental conditions when fast measurement of BVOC species is not available.

  20. The micro-environmental impact of volatile organic compound emissions from large-scale assemblies of people in a confined space

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Large-scale assemblies of people in a con'ned space can exert signi'cant impacts on the local air chemistry due to human emissions of volatile organics. Variations of air-quality in such small scale can be studied by quantifying 'ngerprint volatile organic compounds (VOCs) such as acetone, toluene, ...

  1. Survey of volatile organic compounds associated with automotive emissions in the urban airshed of São Paulo, Brazil

    NASA Astrophysics Data System (ADS)

    Colón, Maribel; Pleil, Joachim D.; Hartlage, Thomas A.; Lucia Guardani, M.; Helena Martins, M.

    The Metropolitan Region of São Paulo (MRSP), Brazil, is one of the largest metropolitan areas in the world (population 17 million, approx.) and relies heavily on alcohol-based fuels for automobiles. It is estimated that about 40% of the total volume of fuel is ethanol with some vehicles using pure ethanol and others a gasoline/ethanol blend. As such, São Paulo is an excellent example of an oxygenates-dominated airshed of mobile sources and is most likely indicative of the future in heavily populated areas in the US such as Los Angeles where "oxy-fuels" are becoming an important replacement for the conventional pure petroleum-based fuels. In this work, we surveyed the ambient air to identify and quantify the organic compounds associated with the evaporative and exhaust emissions of these fuels and to begin to understand the potential for human exposure. Because this was an initial test without detailed prior knowledge of the airshed of the area, we applied two different air sampling methods for various time periods to assess the ambient concentrations of a variety of polar and nonpolar volatile organic compounds (VOCs). For quality assurance (QA), we collected all the samples in duplicate (whole-air samples in Summa canisters and adsorbent-based samples on Perkin-Elmer Air Toxics tubes) at various flow rates to test performance. All samples were collected over identical time frames, typically for 1-, 2-, and 4-h periods per day at six different locations over a period of 1 week. Overall São Paulo results demonstrate that mean concentrations of single-ring aromatics are 2-3 times higher, volatile aldehydes are 5-10 times higher, and simple alcohols 10-100 times higher as compared to results of a recent study performed by EPA in the Los Angeles basin. C 4-C 11n-alkanes were only slightly elevated in São Paulo.

  2. Air pollutant emissions from on-road vehicles in China, 1999-2011.

    PubMed

    Lang, Jianlei; Cheng, Shuiyuan; Zhou, Ying; Zhang, Yonglin; Wang, Gang

    2014-10-15

    The on-road vehicular emission in China from 1999 to 2011 was estimated, based on the emission factors of vehicles with different emission standards calculated by the COPERT model. The CO, NMVOC, NOX, BC and OC emissions changed from 19.7 Tg, 4.4 Tg, 2.3 Tg, 47.1 Gg and 74.4 Gg in 1999 to 32.7 Tg, 4.1 Tg, 7.6 Tg, 177.6 Gg and 101.5 Gg in 2011, respectively. The general trend for CO, NOX and BC was increasing, while the tendency for NMVOC and OC was firstly increase before 2002 and then decrease from 2003. The spatial analysis results showed that high emissions occurred in developed provinces (Guangdong, Shandong, Hebei, Jiangsu and Henan). The correlation between vehicular emissions and GDP were further investigated and good linear correlation was found. The not-obvious change of the inter-annual (1999-2011) fitted straight line slope and the sustained increasing emissions for NOX and BC suggested that the challenge of mitigating vehicular NOX and BC emissions is severe in China. The contribution from different vehicle types was also analyzed. Passenger car (PC) and motorcycle (MC) was the main contributor to the CO and NMVOC emissions. However, the contribution ratio of MC was decreasing from 36.6% and 68.8% in 1999 to 15.7% and 25.7% in 2011. Heavy duty truck (HDT) was the dominant contributor to NOX, BC and OC, with proportions of 58.9%, 57.6% and 52.8% in 2011, respectively. In addition, the uncertainty of the estimated emissions was also assessed based on the Monte Carlo simulation.

  3. Estimation of volatile compounds emission rates from the working face of a large anaerobic landfill in China using a wind tunnel system

    NASA Astrophysics Data System (ADS)

    Liu, Yanjun; Lu, Wenjing; Li, Dong; Guo, Hanwen; Caicedo, Luis; Wang, Chi; Xu, Sai; Wang, Hongtao

    2015-06-01

    Municipal solid waste landfills are one of the major sources of odor complaints. The determination of volatile compounds (VCs) emissions and their rates is a necessary prerequisite to calculate and study VCs dispersion and control. In this study a wind tunnel system has been introduced to investigate the VCs emission rates from the working face of a large anaerobic landfill in China. The VCs in gas samples were characterized by gas-chromatograph-mass-spectrometer. The emission rates of VCs increased linearly with sweeping velocity (0.1 m·s-1 to 0.5 m·s-1), and 0.28 m·s-1 was selected as the recommended practical operation sweeping velocity. The VCs emission rates on the working face at the landfill site were investigated during the course of a day. 31 chemical species divided into six chemical groups were quantified with the following emission rates: oxygenated compounds: 205.73-750.00 μg·m-2·s-1, hydrocarbons: 61.82-220.37 μg·m-2·s-1, aromatics: 15.55-40.11 μg·m-2·s-1, halogenated compounds: 11.71-31.57 μg·m-2·s-1, terpenes: 2.71-18.70 μg·m-2·s-1, and sulfur compounds: 1.29-10.84 μg·m-2·s-1. The highest average emission rates of VCs were found from midnight to dawn (1:00-7:00). These results provide key input parameters to users of VCs dispersion models to calculate buffer distances.

  4. Real-world emissions of carbonyl compounds from in-use heavy-duty diesel trucks and diesel Back-Up Generators (BUGs)

    NASA Astrophysics Data System (ADS)

    Sawant, Aniket A.; Shah, Sandip D.; Zhu, Xiaona; Miller, J. Wayne; Cocker, David R.

    Emissions of carbonyl compounds such as formaldehyde, acetaldehyde, and acrolein are of interest to the scientific and regulatory communities due to their suspected or likely impacts on human health. The present work investigates emissions of carbonyl compounds from nine Class 8 heavy-duty diesel (HDD) tractors and also from nine diesel-powered backup generators (BUGs); the former were chosen because of their ubiquity as an emission source, and the latter because of their proximity to centers of human activity. The HDD tractors were operated on the ARB 4-Mode heavy heavy-duty diesel truck (HHDDT) driving cycle, while the BUGs were operated on the ISO 8178 Type D2 5-mode steady-state cycle and sampled using a mobile emissions laboratory (UCR MEL) equipped with a full-scale dilution tunnel. Samples were analyzed using the SAE930142 (Auto/Oil) method for 11 aldehydes, from formaldehyde to hexanaldehyde, and 2 ketones (acetone and methyl ethyl ketone). Although absolute carbonyl emissions varied widely by BUG, the relative contributions of the different carbonyls were similar (e.g., median: 56% for formaldehyde). A slight increasing trend with engine load was observed for relative formaldehyde contribution, but not for acetaldehyde contribution, for the BUGs. On-road per-mile carbonyl emission factors were a strong function of operating mode of the ARB HHDDT cycle, and found to decrease in the order Creep>Transient>Cruise. This order is qualitatively similar to emission factors for PAHs and n-alkanes determined for the same set of Class 8 diesel tractors in an earlier work. In general, relative carbonyl contributions for the HDD tractors were similar to those for BUGs (e.g., median: 54% for formaldehyde). These results indicate that while engine operating mode and application appear to exert a strong influence on the total absolute mass emission rate of the carbonyls measured, they do not appear to exert as strong an influence on the relative mass emission rates of

  5. Implementation and evaluation of a comprehensive emission model for Europe

    NASA Astrophysics Data System (ADS)

    Bieser, Johannes; Aulinger, Armin; Matthias, Volker; Quante, Markus

    2010-05-01

    Crucial input data sets for Chemical Transport Models (CTM) are the meteorological fields and the emissions data. While there are several publicly available meteorological models, the situation for European emission models is still different. European emissions data either lack spatial and temporal resolution, only cover specific countries or are proprietary and not free to use. In this work the US EPA emission model SMOKE (Sparse Matrix Operator Kernel Emissions) has been successfully adapted and partially extended to create European emissions input for CTMs. The modified version of the SMOKE emission model (SMOKE/E) uses official and publicly available data sets and statistics to create emissions of CO, NOx, SO2, NH3, PM2.5, PM10, NMVOC. Currently it supports VOC splits for several photochemical mechanisms, namely CB4, CB5 and RADM2. PM2.5 is split into elemental carbon, organic carbon, sulfate, nitrate and other particles. Additionally emissions of benzo[a]pyrene (BaP) have been modelled with SMOKE Europe. The temporal resolution of the emissions is one hour, the horizontal resolution is up to 1x1 km². SMOKE/E also implements plume in grid calculations for vertical distribution of point sources. The vertical resolution is infinitely variable and is implemented in the form of pressure levels. The area covered by the emission model at this point is Europe and it's surrounding countries, including north Africa and parts of Asia. Thus far SMOKE Europe has been used to create European emissions on a 54x54km² grid covering the whole of Europe and a 18x18km² nested grid over the North and Baltic Sea for the years 1990-2006. The currently implemented datasets allow for the calculation of emissions between 1970-2010. Besides this future emissions scenarios for the timespan 2010-2020 are being calculated using the EMEP projections. The created emissions have been statistically compared to the gridded EMEP emissions as well as to data from other emission models for the

  6. Surface emission determination of volatile organic compounds (VOC) from a closed industrial waste landfill using a self-designed static flux chamber.

    PubMed

    Gallego, E; Perales, J F; Roca, F J; Guardino, X

    2014-02-01

    Closed landfills can be a source of VOC and odorous nuisances to their atmospheric surroundings. A self-designed cylindrical air flux chamber was used to measure VOC surface emissions in a closed industrial landfill located in Cerdanyola del Vallès, Catalonia, Spain. The two main objectives of the study were the evaluation of the performance of the chamber setup in typical measurement conditions and the determination of the emission rates of 60 different VOC from that industrial landfill, generating a valuable database that can be useful in future studies related to industrial landfill management. Triplicate samples were taken in five selected sampling points. VOC were sampled dynamically using multi-sorbent bed tubes (Carbotrap, Carbopack X, Carboxen 569) connected to SKC AirCheck 2000 pumps. The analysis was performed by automatic thermal desorption coupled with a capillary gas chromatograph/mass spectrometry detector. The emission rates of sixty VOC were calculated for each sampling point in an effort to characterize surface emissions. To calculate average, minimum and maximum emission values for each VOC, the results were analyzed by three different methods: Global, Kriging and Tributary area. Global and Tributary area methodologies presented similar values, with total VOC emissions of 237 ± 48 and 222 ± 46 g day(-1), respectively; however, Kriging values were lower, 77 ± 17 gd ay(-1). The main contributors to the total emission rate were aldehydes (nonanal and decanal), acetic acid, ketones (acetone), aromatic hydrocarbons and alcohols. Most aromatic hydrocarbon (except benzene, naphthalene and methylnaphthalenes) and aldehyde emission rates exhibited strong correlations with the rest of VOC of their family, indicating a possible common source of these compounds. B:T ratio obtained from the emission rates of the studied landfill suggested that the factors that regulate aromatic hydrocarbon distributions in the landfill emissions are different from the ones

  7. The contribution of vehicular emission to the atmospheric concentrations of carbon compounds in the Metropolitan Area of Sao Paulo

    NASA Astrophysics Data System (ADS)

    Andrade, M.; Fornaro, A.; Miranda, R.; Ynoue, R. Y.; Freitas, E. D.; LAPAt-Laboratorio de Analise dos Processos Atmosfericos

    2013-05-01

    It is recognized that megacities have regional and global effects on climate, and that aerosols and Green House Gases (GHG) constitute the principal tracer of those effects. Such is the case in the Metropolitan Area of Sao Paulo (MASP), one of the largest mega-cities in the world. MASP has a population of almost 20 million inhabitants. The main source of air pollution is the transport sector. In this region, there are approximately 6.5 million passenger cars and commercial vehicles: 85% light duty, 3% heavy-duty diesel vehicles (diesel + 3% bio-diesel) and 12% motorcycles. Of the light duty vehicle, approximately 55% burn a mixture (v/v) of 78% gasoline with 22% ethanol (referred to as gasohol), 4% use hydrated ethanol (95% ethanol + 5% water), 38% flexible fuel vehicles capable of burning both gasohol as hydrated ethanol, and 2% use diesel. In average 50% of the fuel used in MASP is ethanol what brings the necessity of more studies to understand the formation of photochemical oxidants and secondary particles. According to the São Paulo State Environmental Protection Agency, 97% of carbon monoxide (CO), 85% of hydrocarbons (HC), 82% of nitrogen oxides (NOx), 36% of sulfur dioxide emitted, and 36% of all inhalable particulate matter (PM10) are emitted by the vehicular fleet. Concerning particles, 75% of the Fine Particle Concentration is related to the burning of fuel, mainly diesel. The fine particles are composed of Organic Carbon (40%), Black Carbon (30%), ions (15%) and metals. It is known that the soot is warming the climate and is important to the radiative balance. Another important driver to the radiative balance, the CO2 is mainly emitted by the transport sector, which is responsible for 57% of its emission. A comprehensive project under development has the objective of determine the role of MASP as the source of gaseous and particle compounds to the atmosphere of the region and in a mesoscale perspective. The project with funding from the São Paulo

  8. Using IASI and MIPAS in combination to characterise CO and other volatile organic compound emissions from fires

    NASA Astrophysics Data System (ADS)

    Moore, David; Sembhi, Harjinder; Remedios, John; Tereszchuk, Keith

    2013-04-01

    Short-lived species emitted from wildfires, such as carbon monoxide (CO) and volatile organic compounds (VOCs), carry a lot of information on atmospheric processes relating to chemistry, convection and emission. These disruptive events are indirectly a climatological feature of the Earth's atmosphere and its climate response and occur at sufficient frequency to make studying and understanding biomass plume chemistry vital. Accurate measurement of trace gases from these events will also aid improvements in climate/chemistry models. In this study, we utilise IASI, MIPAS and ACE data to derive wildfire emissions of VOCs, in the context of two periods; the early 2009 Black Saturday fires and the BORTAS campaign fires. Using the complementary viewing angles of IASI (nadir) and MIPAS/ACE (limb), results will be shown which illustrate observations of aged plume composition, chemistry, distribution and area along with information about vertical distribution. The Black Saturday fires were a particularly severe event over South-Eastern Australia which burnt an area of 450,000 km2, with up to 400 individual fires being identified on February 7th 2009 alone. Driven by weeks of little or no rainfall and record-breaking temperatures, we show that the plumes from this event, contained enhanced VOC amounts and mixed within the lower stratosphere, reaching altitudes up to 18 km. Enhancement ratios, using CO as a reference, show potential secondary formation of HCOOH within the plume. We are able to track the evolution of the plume with IASI data for up to 20 days after the initial event. The second case study is comparison to results from a recent aircraft campaign over North America in July/August 2011 (BORTAS). The NERC-funded campaign was dedicated to studying the impact of local pollution events over North America and aged plumes originated from Asia and Siberia. In the context of the campaign aims, we investigated CO, VOC chemistry and aerosol signatures in boreal biomass

  9. Particulate Matter Sampling and Volatile Organic Compound Removal for Characterization of Spark Ignited Direct Injection Engine Emissions

    SciTech Connect

    Matthias, Nick; Farron, Carrie; Foster, David E.; Andrie, Mike; Krieger, Roger; Najt, Paul; Narayanaswamy, Kushal; Solomon, Arun; Zelenyuk, Alla

    2012-01-01

    More stringent emissions regulations are continually being proposed to mitigate adverse human health and environmental impacts of internal combustion. With that in mind, it has been proposed that vehicular particulate matter (PM) emissions should be regulated based on particle number in addition to particle mass. One aspect of this project is to study different sample handling methods for number based aerosol measurements, specifically, two different methods for removing volatile organic compounds (VOCs) from an aerosol sample. One method is a Dekati Thermodenuder (TD) and the other is an evaporative chamber/diluter (EvCh). These sample handling methods have been implemented for this project in an engine test cell built around a direct injection spark ignited (DISI) engine. The engine was designed for stoichiometric, homogeneous combustion. Direct injection is of particular interest for improved fuel efficiency but this comes with the production of a significant amount of (PM) and may therefore be subject to the proposed number based regulation. Another aspect of this project is to characterize PM from this engine in terms of particle number and composition. The first interesting observation is that PM number distributions, acquired using a TSI SMPS, have a large accumulation mode (30-294 nm) but a very small nuclei mode (8-30 nm). This is understood to represent a lack of condensation particles meaning that neither the exhaust conditions nor the sample handling conditions are conducive to condensation. This lack of nuclei mode does not, however, represent a lack of VOCs in the sample. It has been observed, using mass spectral analysis (limited to PM>50 nm), that PM from the DISI engine has approximately 40% organic content through varying operating conditions. This begs the question of how effective different sample handling methods are at removing these VOCs. For one specific operating condition, called Cold Start, the un-treated PM was 40% organic. The TD

  10. Observations and models of emissions of volatile terpenoid compounds from needles of ponderosa pine trees growing in situ: control by light, temperature and stomatal conductance

    SciTech Connect

    Harley, Peter; Eller, Allyson; Guenther, Alex; Monson, Russell K.

    2014-07-12

    Terpenoid emissions from ponderosa pine (Pinus ponderosa subsp. scopulorum) were measured in Colorado, USA over two growing seasons to evaluate the role of incident light, needle temperature and stomatal conductance in controlling emissions of 2-methyl-3-buten-2-ol (MBO) and several monoterpenes. MBO was the dominant daylight terpenoid emission, comprising on average 87% of the total flux, and diurnal variations were largely determined by light and temperature. During daytime, oxygenated monoterpenes (especially linalool) comprised up to 75% of the total monoterpenoid flux from needles. A significant fraction of monoterpenoid emissions was light dependent and 13CO2 labeling studies confirmed de novo production. Thus, modeling of monoterpenoid emissions required a hybrid model in which a significant fraction of emissions was dependent on both light and temperature, while the remainder was dependent on temperature alone. Experiments in which stomata were forced to close using abscisic acid demonstrated that MBO and a large fraction of the monoterpene flux, presumably linalool, could be limited at the scale of seconds to minutes by stomatal conductance. Using a previously published model of terpenoid emissions which explicitly accounts for the physico-chemical properties of emitted compounds, we are able to simulate these observed stomatal effects, whether induced through experimentation or arising under naturally fluctuation conditions of temperature and light. This study shows unequivocally that, under naturally occurring field conditions, de novo light dependent monoterpenes can comprise a large fraction of emissions. Differences between the monoterpene composition of ambient air and needle emissions imply a significant non-needle emission source enriched in Δ-3-carene.

  11. Observations and models of emissions of volatile terpenoid compounds from needles of ponderosa pine trees growing in situ: control by light, temperature and stomatal conductance.

    PubMed

    Harley, Peter; Eller, Allyson; Guenther, Alex; Monson, Russell K

    2014-09-01

    Terpenoid emissions from ponderosa pine (Pinus ponderosa subsp. scopulorum) were measured in Colorado, USA over two growing seasons to evaluate the role of incident light, needle temperature, and stomatal conductance in controlling emissions of 2-methyl-3-buten-2-ol (MBO) and several monoterpenes. MBO was the dominant daylight terpenoid emission, comprising on average 87% of the total flux, and diurnal variations were largely determined by light and temperature. During daytime, oxygenated monoterpenes (especially linalool) comprised up to 75% of the total monoterpenoid flux from needles. A significant fraction of monoterpenoid emissions was dependent on light and 13CO2 labeling studies confirmed de novo production. Thus, modeling of monoterpenoid emissions required a hybrid model in which a significant fraction of emissions was dependent on both light and temperature, while the remainder was dependent on temperature alone. Experiments in which stomata were forced to close using abscisic acid demonstrated that MBO and a large fraction of the monoterpene flux, presumably linalool, could be limited at the scale of seconds to minutes by stomatal conductance. Using a previously published model of terpenoid emissions, which explicitly accounts for the physicochemical properties of emitted compounds, we were able to simulate these observed stomatal effects, whether induced experimentally or arising under naturally fluctuation conditions of temperature and light. This study shows unequivocally that, under naturally occurring field conditions, de novo light-dependent monoterpenes comprise a significant fraction of emissions in ponderosa pine. Differences between the monoterpene composition of ambient air and needle emissions imply a significant non-needle emission source enriched in Δ-3-carene.

  12. Evaluation of the Industrial Point Source Emission Inventory for the Houston Ship Channel Area Using Ship-Based, High-Time-Resolution Measurements of Volatile Organic Compounds

    NASA Astrophysics Data System (ADS)

    Bon, D.; de Gouw, J. A.; Gilman, J. B.; Kuster, W. C.; Lerner, B. M.; Williams, E. J.; Frost, G. J.

    2010-12-01

    Proton Transfer Reaction Ion Trap Mass Spectrometry (PIT-MS) was used to characterize several large (>100 ppbv) industrial volatile organic compound (VOC) plumes in the Houston, Texas Ship Channel observed from the NOAA R/V Ronald H. Brown during the 2006 Texas Air Quality Study (TexAQS) field campaign. Because the ship was sampling close to numerous large emission sources, many of the observed plumes were highly transient making the PIT-MS, with its high time resolution and continuous full mass scan capability, a very useful tool for VOC characterization of the plumes. Plume compositions are compared to the TexAQS2K6 Houston-Galveston-Brazoria Point Source Emission Inventory for individual aromatic compounds; oxygenated VOCs and other selected industrial VOCs observed by PIT-MS. In many cases, we do not find good agreement between the measured plume composition and the VOC speciation in the emissions inventory. These observations are not surprising, as previous research has shown that emission fluxes of individual VOCs may be underestimated by as much as 1-2 orders of magnitude in inventories for the Houston area. In many cases, PIT-MS measurements show clear evidence of industrial emissions not previously identified by the Proton Transfer Reaction (PTR) method. The frequent lack of correlation between large VOC enhancements and enhancements in SO2, NOx and CO suggests large, non-combustion sources of VOCs.

  13. Volatile organic compound emissions induced by the aphid Myzus persicae differ among resistant and susceptible peach cultivars and a wild relative.

    PubMed

    Staudt, Micheal; Jackson, Benjamin; El-Aouni, Hanane; Buatois, Bruno; Lacroze, Jean-Philippe; Poëssel, Jean-Luc; Sauge, Marie-Helene

    2010-10-01

    Little is known on aphid-induced emissions of volatile organic compounds (VOCs) from trees and particularly on their intraspecific variability in association with resistance traits. We compared VOC emissions from five peach cultivars (Prunus persica (L.) Batsch) and a wild relative (Prunus davidiana (Carrière) Franch) that differ in their level (susceptible/resistant) and type (antixenosis, antibiosis) of resistance to the green peach aphid, Myzus persicae (Sulzer). Additionally, the kinetics of VOC induction in response to aphids was compared with that by mechanical wounding. Qualitative and overall quantitative differences among peach genotypes were found in VOC emissions that were mainly composed of methyl-salicylate, farnesenes, (E)-β-ocimene and (E)-4,8-dimethyl-1,3,7-nonatriene. Irrespective of the type of resistance, all resistant genotypes had increased VOC emissions upon aphid attack, while in susceptible genotypes emissions remained low. Emission increases were highest in the genotypes that express increased aphid resistance during second infestations, which had also the highest proportions of methyl-salicylate in their emissions. VOC induction by aphids proceeded slowly with a delay of several hours. Artificial wounding of leaves did not result in emissions of aphid-induced VOCs but caused an immediate burst of green leaf volatiles and benzaldehyde. We conclude that VOC induction in resistant peach cultivars is part of a general defence syndrome that is being avoided or suppressed by M. persicae in the susceptible genotypes. The induction likely involves an aphid-specific elicitor and (methyl)-salicylate in the subsequent signalling and regulation processes that should include gene activation due to the marked delay in the emission response. The results are compared with those of the literature and discussed in view of their ecological and environmental significance.

  14. Volatile organic compound and particulate emission studies of AF (Air Force) paint-booth facilities. Phase 1. Final report, February-December 1987

    SciTech Connect

    Ayer, J.; Wolbach, D.

    1988-07-01

    This study presents the results of volatile organic compound (VOC) and particulate emission surveys performed at three Air Force painting facilities. The three facilities -- one in McClellan AFB buildings 655 and two at Travis AFB in buildings 550 and 1014 -- did not meet local VOC emission standards. The possibility of reducing these emissions with recirculation modifications and various VOC reduction and control strategies is discussed. Although VOC emissions from paint spray booths can be controlled by add-on control systems, control is expensive for present air flow rates. The use of air recirculation within the spray booth can reduce the cost of VOC emission controls by reducing the quantity of air that requires processing. Recirculation systems were designed for two of the painting facilities included in this study. In designing the systems, various criteria such as paint booth VOC concentrations and health and safety standards were considered. Add-on VOC emission-control systems that can be used in conjunction with the recirculation system are evaluated. The devices of interest are a solvent incineration system and an activated-carbon adsorption bed. The VOC removal efficiency, initial capital investment and operating costs for both of these technologies are discussed.

  15. Real-time analysis of organic compounds in ship engine aerosol emissions using resonance-enhanced multiphoton ionisation and proton transfer mass spectrometry.

    PubMed

    Radischat, Christian; Sippula, Olli; Stengel, Benjamin; Klingbeil, Sophie; Sklorz, Martin; Rabe, Rom; Streibel, Thorsten; Harndorf, Horst; Zimmermann, Ralf

    2015-08-01

    Organic combustion aerosols from a marine medium-speed diesel engine, capable to run on distillate (diesel fuel) and residual fuels (heavy fuel oil), were investigated under various operating conditions and engine parameters. The online chemical characterisation of the organic components was conducted using a resonance-enhanced multiphoton ionisation time-of-flight mass spectrometer (REMPI TOF MS) and a proton transfer reaction-quadrupole mass spectrometer (PTR-QMS). Oxygenated species, alkenes and aromatic hydrocarbons were characterised. Especially the aromatic hydrocarbons and their alkylated derivatives were very prominent in the exhaust of both fuels. Emission factors of known health-hazardous compounds (e.g. mono- and poly-aromatic hydrocarbons) were calculated and found in higher amounts for heavy fuel oil (HFO) at typical engine loadings. Lower engine loads lead in general to increasing emissions for both fuels for almost every compound, e.g. naphthalene emissions varied for diesel fuel exhaust between 0.7 mg/kWh (75 % engine load, late start of injection (SOI)) and 11.8 mg/kWh (10 % engine load, late SOI) and for HFO exhaust between 3.3 and 60.5 mg/kWh, respectively. Both used mass spectrometric techniques showed that they are particularly suitable methods for online monitoring of combustion compounds and very helpful for the characterisation of health-relevant substances. Graphical abstract Three-dimensional REMPI data of organic species in diesel fuel and heavy fuel oil exhaust.

  16. Developmental patterns of emission of scent compounds and related gene expression in roses of the cultivar Rosa x hybrida cv. 'Yves Piaget'.

    PubMed

    Chen, Xiaomin; Baldermann, Susanne; Cao, Shuyan; Lu, Yao; Liu, Caixia; Hirata, Hiroshi; Watanabe, Naoharu

    2015-02-01

    2-Phenylethanol (2PE) and 3,5-dimethoxytoluene (DMT) are characteristic scent compounds in specific roses such as Rosa x hybrida cv. 'Yves Piaget'. We analyzed the endogenous concentrations and emission of 2PE and DMT during the unfurling process in different floral organs, as well as changes in transcript levels of the two key genes, PAR and OOMT2. The emission of both 2PE and DMT increased during floral development to reach peaks at the fully unfurled stage. The relative transcripts of PAR and OOMT2 also increased during floral development. Whereas the maximum for OOMT2 was found at the fully unfurled stage (stage 4), similar expression levels of PAR were detected at stage 4 and the senescence stage (stage 6). The results demonstrate a positive correlation between the expression levels of PAR and OOMT2 and the emission of 2PE and DMT. In addition, endogenous volatiles and relative transcripts showed tissue- and development-specific patterns.

  17. Exhaust emissions of volatile organic compounds of powered two-wheelers: effect of cold start and vehicle speed. Contribution to greenhouse effect and tropospheric ozone formation.

    PubMed

    Costagliola, M Antonietta; Murena, Fabio; Prati, M Vittoria

    2014-01-15

    Powered two-wheeler (PTW) vehicles complying with recent European type approval standards (stages Euro 2 and Euro 3) were tested on chassis dynamometer in order to measure exhaust emissions of about 25 volatile organic compounds (VOCs) in the range C1-C7, including carcinogenic compounds as benzene and 1,3-butadiene. The fleet consists of a moped (engine capacity ≤ 50 cm(3)) and three fuel injection motorcycles of different engine capacities (150, 300 and 400 cm(3)). Different driving conditions were tested (US FPT cycle, constant speed). Due to the poor control of the combustion and catalyst efficiency, moped is the highest pollutant emitter. In fact, fuel injection strategy and three way catalyst with lambda sensor are able to reduce VOC motorcycles' emission of about one order of magnitude with respect to moped. Cold start effect, that is crucial for the assessment of actual emission of PTWs in urban areas, was significant: 30-51% of extra emission for methane. In the investigated speed range, moped showed a significant maximum of VOC emission factor at minimum speed (10 km/h) and a slightly decreasing trend from 20 to 60 km/h; motorcycles showed on the average a less significant peak at 10 km/h, a minimum at 30-40 km/h and then an increasing trend with a maximum emission factor at 90 km/h. Carcinogenic VOCs show the same pattern of total VOCs. Ozone Formation Potential (OFP) was estimated by using Maximum Incremental Reactivity scale. The greatest contribution to tropospheric ozone formation comes from alkenes group which account for 50-80% to the total OFP. VOC contribution effect on greenhouse effect is negligible with respect to CO2 emitted.

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

    EPA Science Inventory

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

  19. Assessment of China's virtual air pollution transport embodied in trade by a consumption-based emission inventory

    NASA Astrophysics Data System (ADS)

    Zhao, H. Y.; Zhang, Q.; Davis, S. J.; Guan, D.; Liu, Z.; Huo, H.; Lin, J. T.; Liu, W. D.; He, K. B.

    2014-10-01

    High anthropogenic emissions from China have resulted in serious air pollution, and it has attracted considerable academic and public concern. The physical transport of air pollutants in the atmosphere has been extensively investigated, however, understanding the mechanisms how the pollutants were transferred through economic and trade activities remains challenge. In this work, we assessed China's virtual air pollutant transport embodied in trade, by using consumption-based accounting approach. We first constructed a consumption-based emission inventory for China's four key air pollutants (primary PM2.5, sulfur dioxide (SO2), nitrogen oxides (NOx) and non-methane volatile organic compounds (NMVOC)) in 2007, based on the bottom-up sectoral emission inventory concerning their production activities - a production-based inventory. We used a multiregional input-output (MRIO) model to integrate the sectoral production-based emissions and the associated economic and trade activities, and finally obtained consumption-based inventory. Unlike the production-based inventory, the consumption-based inventory tracked emissions throughout the supply chain related to the consumption of goods and services and hereby identified the emission flows followed the supply chains. From consumption-based perspective, emissions were significantly redistributed among provinces due to interprovincial trade. Large amount of emissions were embodied in the net imports of east regions from northern and central regions; these were determined by differences in the regional economic status and environmental policies. We also calculated the emissions embodied in exported and imported goods and services. It is found that 15-23% of China's pollutant emissions were related to exports for foreign consumption; that proportion was much higher for central and export-oriented coastal regions. It is suggested that measures should be introduced to reduce air pollution by integrating cross-regional consumers

  20. Volatile organic compounds (VOCs) emission characteristics and control strategies for a petrochemical industrial area in middle Taiwan.

    PubMed

    Yen, Chia-Hsien; Horng, Jao-Jia

    2009-11-01

    This study investigated VOC emissions from the largest petrochemical industrial district in Taiwan and recommended some control measures to reduce VOC emissions. In addition to the petrochemical industry, the district encompasses a chemical and fiber industry, a plastics industry and a harbor, which together produce more than 95% of the VOC emissions in the area. The sequence of VOC emission was as follows: components (e.g., valves, flanges, and pumps) (47%) > tanks (29%) > stacks (15%) > wastewater treatment facility (6%) > loading (2%) > flares (1%). Other plants producing high-density polyethylene (HDPE), styrene, ethylene glycol (EG), gas oil, and iso-nonyl-alchol (INA) were measured to determine the VOC leaching in the district. The VOC emissions of these 35 plants (90% of all plants) were less than 100 tons/year. About 74% of the tanks were fixed-roof tanks that leached more VOCs than the other types of tanks. To reduce leaching, the components should be checked periodically, and companies should be required to follow the Taiwan EPA regulations. A VOC emission management system was developed in state implementation plans (SIPs) to inspect and reduce emissions in the industrial district.

  1. Measurements of volatile organic compounds at a suburban ground site (T1) in Mexico City during the MILAGRO 2006 campaign: Measurement comparison, emission ratios, and source attribution

    SciTech Connect

    Bon, D.M.; Springston, S.; M.Ulbrich, I.; de Gouw, J. A.; Warneke, C.; Kuster, W. C.; Alexander, M. L.; Baker, A.; Beyersdorf, A. J.; Blake, D.; Fall, R.; Jimenez, J. L., Herndon, S. C.; Huey, L. G.; Knighton, W. B.; Ortega, J.; Vargas, O.

    2011-03-16

    Volatile organic compound (VOC) mixing ratios were measured with two different instruments at the T1 ground site in Mexico City during the Megacity Initiative: Local and Global Research Observations (MILAGRO) campaign in March of 2006. A gas chromatograph with flame ionization detector (GC-FID) quantified 18 light alkanes, alkenes and acetylene while a proton-transfer-reaction ion-trap mass spectrometer (PIT-MS) quantified 12 VOC species including oxygenated VOCs (OVOCs) and aromatics. A GC separation system was used in conjunction with the PIT-MS (GC-PIT-MS) to evaluate PIT-MS measurements and to aid in the identification of unknown VOCs. The VOC measurements are also compared to simultaneous canister samples and to two independent proton-transfer-reaction mass spectrometers (PTR-MS) deployed on a mobile and an airborne platform during MILAGRO. VOC diurnal cycles demonstrate the large influence of vehicle traffic and liquid propane gas (LPG) emissions during the night and photochemical processing during the afternoon. Emission ratios for VOCs and OVOCs relative to CO are derived from early-morning measurements. Average emission ratios for non-oxygenated species relative to CO are on average a factor of {approx}2 higher than measured for US cities. Emission ratios for OVOCs are estimated and compared to literature values the northeastern US and to tunnel studies in California. Positive matrix factorization analysis (PMF) is used to provide insight into VOC sources and processing. Three PMF factors were distinguished by the analysis including the emissions from vehicles, the use of liquid propane gas and the production of secondary VOCs + long-lived species. Emission ratios to CO calculated from the results of PMF analysis are compared to emission ratios calculated directly from measurements. The total PIT-MS signal is summed to estimate the fraction of identified versus unidentified VOC species.

  2. BIOGENIC VOLATILE ORGANIC COMPOUND EMISSIONS (BVOCS) II. LANDSCAPE FLUX POTENTIALS FROM THREE CONTINENTAL SITES IN THE U.S.

    EPA Science Inventory

    Landscape flux potentials for biogenic volatile organic compounds (BVOCs) were derived for three ecosystems in the continental U. S. (Fernbank Forest, Atlanta, GA; Willow Creek, Rhinelander, WI; Temple Ridge, CO). Analytical data from branch enclosure measurements reported in a ...

  3. SEASONAL AND ANNUAL MODELING OF REDUCED NITROGEN COMPOUNDS OVER THE EASTERN UNITED STATES: EMISSIONS, AMBIENT LEVELS, AND DEPOSITION AMOUNTS

    EPA Science Inventory

    Detailed description of the distributions and seasonal trends of atmospheric nitrogen compounds is of considerable interest given their role in formation of acidic substances, tropospheric ozone and particulate matter and nutrient loading effects resulting from their deposition t...

  4. The impact of China's vehicle emissions on regional air quality in 2000 and 2020: a scenario analysis

    NASA Astrophysics Data System (ADS)

    Saikawa, E.; Kurokawa, J.; Takigawa, M.; Mauzerall, D. L.; Horowitz, L. W.; Ohara, T.

    2011-04-01

    The number of vehicles in China has been increasing rapidly. We evaluate the impact of current and possible future vehicle emissions from China on Asian air quality. We modify the Regional Emission Inventory in Asia (REAS) for China's road transport sector in 2000 using updated Chinese data for vehicle numbers, annual mileage and emission factors. We develop two scenarios for 2020: a scenario where emission factors remain the same as they were before any regulation was implemented (business-as-usual, BAU), and a scenario where Euro 3 vehicle emission standards are applied to all vehicles (except motorcycles and rural vehicles). The Euro 3 scenario is an approximation of what may be the case in 2020 as, starting in 2008, all new gasoline and diesel vehicles in China (except motorcycles) were required to meet the Euro 3 emission standards. Using the Weather Research and Forecasting model coupled with Chemistry (WRF/Chem), we examine the regional air quality response to China's vehicle emissions in 2000 and in 2020 for the BAU and Euro 3 scenarios. We evaluate the 2000 model results with observations in Japan, China, Korea, and Russia. Under BAU in 2020, emissions of carbon monoxide (CO), nitrogen oxides (NOx), non-methane volatile organic compounds (NMVOCs), black carbon (BC) and organic carbon (OC) from China's vehicles more than double compared to the 2000 baseline. If all vehicles meet the Euro 3 regulations in 2020, however, these emissions are reduced by more than 50% relative to BAU. The implementation of stringent vehicle emission standards leads to a large, simultaneous reduction of the surface ozone (O3) mixing ratios and particulate matter (PM2.5) concentrations. In the Euro 3 scenario, surface O3 is reduced by more than 10 ppbv and surface PM2.5 is reduced by more than 10 μg m-3 relative to BAU in Northeast China in all seasons. In spring, surface O3 mixing ratios and PM2.5 concentrations in neighboring countries are also reduced by more than 3 ppbv and 1

  5. Organic liquids storage tanks volatile organic compounds (VOCS) emissions dispersion and risk assessment in developing countries: the case of Dar-es-Salaam City, Tanzania.

    PubMed

    Jackson, Msafiri M

    2006-05-01

    The emission estimation of nine volatile organic compounds (VOCs) from eight organic liquids storage tanks companies in Dar-es-Salaam City Tanzania has been done by using US EPA standard regulatory storage tanks emission model (TANKS 4.9b). Total VOCs atmospheric emission has been established to be 853.20 metric tones/yr. It has been established further that petrol storage tanks contribute about 87% of total VOCs emitted, while tanks for other refined products and crude oil were emitting 10% and 3% of VOCs respectively. Of the eight sources (companies), the highest emission value from a single source was 233,222.94 kg/yr and the lowest single source emission value was 6881.87 kg/yr. The total VOCs emissions estimated for each of the eight sources were found to be higher than the standard level of 40,000 kg/yr per source for minor source according to US EPA except for two sources, which were emitting VOCs below the standard level. The annual emissions per single source for each of the VOCs were found to be below the US EPA emissions standard which is 2,000 kg/yr in all companies except the emission of hexane from company F1 which was slightly higher than the standard. The type of tanks used seems to significantly influence the emission rate. Vertical fixed roof tanks (VFRT) emit a lot more than externally floating roof tanks (EFRT) and internally floating roof tanks (IFRT). The use of IFRT and EFRT should be encouraged especially for storage of petrol which had highest atmospheric emission contribution. Model predicted atmospheric emissions are less than annual losses measured by companies in all the eight sources. It is possible that there are other routes for losses beside atmospheric emissions. It is therefore important that waste reduction efforts in these companies are directed not only to reducing atmospheric emissions, but also prevention of the spillage and leakage of stored liquid and curbing of the frequently reported illegal siphoning of stored products

  6. Emission of odorous volatile organic compounds from a municipal manure treatment plant and their removal using a biotrickling filter.

    PubMed

    Li, Jian-Jun; Wu, Yan-Di; Zhang, Yan-Li; Zeng, Pei-Yuan; Tu, Xiang; Xu, Mei-Ying; Sun, Guo-Ping

    2015-01-01

    Odorous volatile organic compounds (VOCs) from municipal manure treatment facilities are considered as a major nuisance issue for operators and nearby residents. In this study, up to 71 odorous VOCs were detected by gas chromatography-mass spectrometry at the manure treatment plant. These compounds can be classified into five different categories, including alkanes, olefins, aromatics, volatile organosulphur compounds and terpenes. Toluene, dimethyl disulphide, dimethyl sulphide, xylene and ethylbenzene were the five most abundant pollutants. A pilot-scale biotrickling filter (BTF) was employed to treat the complex odorous gases. Correlation analysis showed that the removal efficiency (RE) of the BTF was related with the molecular weight and chemical structure of contaminants. Higher than 85% of REs could be reached for aromatic, terpenes and most alkanes compounds after 180 days of operation. Comparatively, most olefins and partial alkanes compounds with a molecular weight lower than 70 were not removed easily. The REs of these compounds ranged from 0% to 94%, and the average removal efficiency (RE) was only about 33.3%.

  7. Root anoxia effects on physiology and emissions of volatile organic compounds (VOC) under short- and long-term inundation of trees from Amazonian floodplains.

    PubMed

    Bracho-Nunez, Araceli; Knothe, Nina Maria; Costa, Wallace R; Maria Astrid, Liberato R; Kleiss, Betina; Rottenberger, Stefanie; Piedade, Maria Teresa Fernandez; Kesselmeier, Jürgen

    2012-01-01

    Volatile organic compound (VOC) emissions are affected by a variety of biotic and abiotic factors such as light intensity, temperature, CO2 and drought. Another stress factor, usually overlooked but very important for the Amazon region, is flooding. We studied the exchange of VOCs in relation to CO2 exchange and transpiration of 8 common tree species from the Amazonian floodplain forest grown up from seeds using a dynamic enclosure system. Analysis of volatile organics was performed by PTR-MS fast online measurements. Our study confirmed emissions of ethanol and acetaldehyde at the beginning of root anoxia after inundation, especially in less anoxia adapted species such as Vatairea guianensis, but not for Hevea spruceana probably due to a better adapted metabolism. In contrast to short-term inundation, long-term flooding of the root system did not result in any emission of ethanol or/and acetaldehyde. Emission of other VOCs, such as isoprenoids, acetone, and methanol exhibited distinct behavior related to the origin (igapó or várzea type of floodplain) of the tree species. Also physiological activities exhibited different response patterns for trees from igapó or várzea. In general, isoprenoid emissions increased within the course of some days of short-term flooding. After a long period of waterlogging, VOC emissions decreased considerably, along with photosynthesis, transpiration and stomatal conductance. However, even under long-term testing conditions, two tree species did not show any significant decrease or increase in photosynthesis. In order to understand ecophysiological advantages of the different responses we need field investigations with adult tree species.

  8. Simulating secondary organic aerosol from missing diesel-related intermediate-volatility organic compound emissions during the Clean Air for London (ClearfLo) campaign

    NASA Astrophysics Data System (ADS)

    Ots, Riinu; Young, Dominique E.; Vieno, Massimo; Xu, Lu; Dunmore, Rachel E.; Allan, James D.; Coe, Hugh; Williams, Leah R.; Herndon, Scott C.; Ng, Nga L.; Hamilton, Jacqueline F.; Bergström, Robert; Di Marco, Chiara; Nemitz, Eiko; Mackenzie, Ian A.; Kuenen, Jeroen J. P.; Green, David C.; Reis, Stefan; Heal, Mathew R.

    2016-05-01

    We present high-resolution (5 km × 5 km) atmospheric chemical transport model (ACTM) simulations of the impact of newly estimated traffic-related emissions on secondary organic aerosol (SOA) formation over the UK for 2012. Our simulations include additional diesel-related intermediate-volatility organic compound (IVOC) emissions derived directly from comprehensive field measurements at an urban background site in London during the 2012 Clean Air for London (ClearfLo) campaign. Our IVOC emissions are added proportionally to VOC emissions, as opposed to proportionally to primary organic aerosol (POA) as has been done by previous ACTM studies seeking to simulate the effects of these missing emissions. Modelled concentrations are evaluated against hourly and daily measurements of organic aerosol (OA) components derived from aerosol mass spectrometer (AMS) measurements also made during the ClearfLo campaign at three sites in the London area. According to the model simulations, diesel-related IVOCs can explain on average ˜ 30 % of the annual SOA in and around London. Furthermore, the 90th percentile of modelled daily SOA concentrations for the whole year is 3.8 µg m-3, constituting a notable addition to total particulate matter. More measurements of these precursors (currently not included in official emissions inventories) is recommended. During the period of concurrent measurements, SOA concentrations at the Detling rural background location east of London were greater than at the central London location. The model shows that this was caused by an intense pollution plume with a strong gradient of imported SOA passing over the rural location. This demonstrates the value of modelling for supporting the interpretation of measurements taken at different sites or for short durations.

  9. Nitrogen saturation in the Rocky Mountains: Linking emissions, deposition, and ecosystem effects using stable isotopes of nitrogen compounds

    USGS Publications Warehouse

    Campbell, D.H.; Nanus, L.; Böhlke, J.K.; Harlin, K.; Collett, J.

    2007-01-01

    Elevated levels of atmospheric N deposition are affecting terrestrial and aquatic ecosystems at high elevations in Rocky Mountain National Park and adjacent areas of the Front Range of Colorado. Federal and state agencies are now working together to develop cost-effective means for reducing atmospheric N deposition. A discussion on N saturation covers the need for better understanding of N emission source areas and source types that contribute to N deposition in the Rocky Mountains Front Range of Colorado; reductions in NO emissions that resulted from Clean Air Act Amendments, which caused NO3 deposition to decrease between 1984 and 2003; factors contributing to N deposition, e.g., rapid population growth and energy development; origins of NO3, e.g., as NO emissions from fossil fuel combustion, including stationary sources (e.g. emission from coal combustion in electric generating units), and mobile sources (vehicle emissions); disperse stationary sources from energy resource development, e.g., natural gas production; and the importance of incorporating local source characterization and finer spatial and temporal sampling into future studies, which could provide additional insight into N deposition source attribution. This is an abstract of a paper presented at the 100th Annual Conference and Exhibition of the Air and Waste Management Association (Pittsburgh, PA 6/26-29/2007).

  10. Liquid-Phase Epitaxy Effective Encapsulation of Lanthanide Coordination Compounds into MOF Film with Homogeneous and Tunable White-Light Emission.

    PubMed

    Gu, Zhi-Gang; Chen, Zheng; Fu, Wen-Qiang; Wang, Fei; Zhang, Jian

    2015-12-30

    As a new family of hybrid inorganic-organic materials with large porosity, metal-organic frameworks (MOFs) have received attractive attention recently on encapsulating functional guest species. Although the encapsulation of luminescent guest into bulk MOFs can tune the luminescent property, the powder composite materials are limited to the application in optical sensors and devices. In the present work, we use a modified liquid-phase epitaxial (LPE) pump method for the fabrication of lanthanide coordination compounds (LCCs)-encapsulated MOF thin film on substrate with high encapsulation efficiency. The resultant composite film reveals an oriented and homogeneous composite film, in which a white light emission by tuning the LCCs of red, blue and green emission can be obtained. This strategy may open new perspectives for developing high-encapsulation-efficiency, oriented, and homogeneous solid-state lighting composite films in the application of optical sensors and devices.

  11. Health risk impacts analysis of fugitive aromatic compounds emissions from the working face of a municipal solid waste landfill in China.

    PubMed

    Liu, Yanjun; Liu, Yanting; Li, Hao; Fu, Xindi; Guo, Hanwen; Meng, Ruihong; Lu, Wenjing; Zhao, Ming; Wang, Hongtao

    2016-12-01

    Aromatic compounds (ACs) emitted from landfills have attracted a lot of attention of the public due to their adverse impacts on the environment and human health. This study assessed the health risk impacts of the fugitive ACs emitted from the working face of a municipal solid waste (MSW) landfill in China. The emission data was acquired by long-term in-situ samplings using a modified wind tunnel system. The uncertainty of aromatic emissions is determined by means of statistics and the emission factors were thus developed. Two scenarios, i.e. 'normal-case' and 'worst-case', were presented to evaluate the potential health risk in different weather conditions. For this typical large anaerobic landfill, toluene was the dominant species owing to its highest releasing rate (3.40±3.79g·m(-2)·d(-1)). Despite being of negligible non-carcinogenic risk, the ACs might bring carcinogenic risks to human in the nearby area. Ethylbenzene was the major health threat substance. The cumulative carcinogenic risk impact area is as far as ~1.5km at downwind direction for the normal-case scenario, and even nearly 4km for the worst-case scenario. Health risks of fugitive ACs emissions from active landfills should be concerned, especially for landfills which still receiving mixed MSW.

  12. Measurements of volatile organic compounds in rural area of Yangtze River Delta region: Measurement comparison and source characterization

    NASA Astrophysics Data System (ADS)

    Kudo, S.; Saito, S.; Tanimoto, H.; Inomata, S.; Kanaya, Y.; Yamaji, K.; Xiaole, P.; Wang, Z.

    2012-12-01

    Concentrations of non-methane volatile organic compounds (NMVOCs) in ambient air were measured by three different methods in a city of Rudong in May and June 2010. Intercomparison of VOCs measurements was made among in-situ measurements and canister analyses with a gas chromatography/flame ionization detection/mass spectrometry (GC/FID/MS) and proton transfer reaction-mass spectrometry (PTR-MS). For 18 VOCs measured by GC/FID/MS, canister analyses and in-situ measurements were in reasonably good agreement (R2 > 0.90). However, alkenes and aromatics in canister samples were found to be lower than in-situ measurements likely due to adsorption of low volatile compounds onto the wall surface inside canisters. For comparison of GC/MS with PTR-MS, the correlations for isoprene, benzene, C8 aromatics, and C9 aromatics were highly significant (R2 ≥ 0.93) with each other. However, there were quantitative differences between GC/MS and PTR-MS. For example, isoprene measured by PTR-MS indicates existence of interferences from C5 alcohols, C5 aldehydes, and furan. During the latter part of the field campaign, elevated concentrations of VOCs and CO were observed when intensive burning of crop residues took place near the sampling site. The concentrations of ethane, propane, ethane, isoprene, acetone, acetaldehyde, and aromatics varied in the range between 0 and 30 ppbv. The observed VOCs concentrations are compared to model results by a regional chemistry-transport model for Asia. The modeled concentrations underestimated the observed concentrations by a factor of 10 for NMHCs, 100 for aromatics, 10 for oxygenated VOCs, implying that current emissions inventories miss a number of sources for these VOCs.

  13. Development of a high-resolution (1 km × 1 km, 1 h) emission model for Spain: The High-Elective Resolution Modelling Emission System (HERMES)

    NASA Astrophysics Data System (ADS)

    Baldasano, José María; Güereca, Leonor Patricia; López, Eugeni; Gassó, Santiago; Jimenez-Guerrero, Pedro

    This work presents the results of the development and application of the High-Elective Resolution Modelling Emission System (HERMES). HERMES generates the emissions for Spain needed for the application of high-resolution chemistry transport models, taking the year 2004 as reference with a temporal resolution of 1 h and a spatial resolution of 1 km 2 considering both anthropogenic (power generation, industrial activities, on-road traffic, ports, airports, solvent use, domestic and commercial fossil fuel use) and biogenic sources (vegetation), using a bottom-up approach, up-to-date information and state-of-the-art methodologies for emission estimation. HERMES is capable of calculating emissions by sector-specific sources or by individual installations and stacks. The annual addition of hourly sectorial emissions leads to an estimation of total annual emissions as follows: NO x, 795 kt; NMVOCs, 1025 kt; CO, 1236 kt; SO 2, 1142 kt and TSP, 180 kt; which are distributed principally in the greater areas of the main cities, highways and large point sources. NO x, SO 2 and PM 2.5 highly correlate with the power generation by coal use, achieving higher emission levels during summertime due to the increase of electricity demand by cooling systems. NMVOCs show high correlation with temperature and solar radiation (mainly as a consequence of the important weight of biogenic emissions) causing the maximum emissions during the daylight hours of summer months. CO emissions are mostly influenced by the on-road traffic; consequently the higher emissions are attained in summer because of the increase of daily average traffic during holidays. The most significant total emission sources are on-road traffic (38%), combustion in power generation plants (33%), biogenic sources (12%) and combustion in manufacturing industries (9%). The inventory generated with HERMES emission model has been successfully integrated within the Spanish Ministry of the Environment's air quality forecasting

  14. Simultaneous determination of chlorinated organic compounds from environmental samples using gas chromatography coupled with a micro electron capture detector and micro-plasma atomic emission detector

    NASA Astrophysics Data System (ADS)

    Quan, Xie; Chen, Shuo; Platzer, Bernhard; Chen, Jingwen; Gfrerer, Marion

    2002-01-01

    Water and sediment samples were screened simultaneously for the presence of polychlorinated organic compounds using gas chromatography (GC) coupled with an micro electron capture detector (μ-ECD) and a newly developed helium plasma based on a micro-atomic emission detector (μ-AED). The GC column effluent was split 15:85 between two detectors. In this way, two chromatograms, one obtained by μ-ECD and another by μ-AED, were recorded simultaneously. α-, β-hexachlorocyclohexane and p, p'-DDE were detected. RSDs of the monitoring results from the two detection methods were <20% for the three compounds. A detection limit of 8.5 pg and at least 3 orders of magnitude of linear range for μ-AED was observed.

  15. Canopy-scale flux measurements and bottom-up emission estimates of volatile organic compounds from a mixed oak and hornbeam forest in northern Italy

    NASA Astrophysics Data System (ADS)

    Acton, W. J. F.; Schallhart, S.; Langford, B.; Valach, A.; Rantala, P.; Fares, S.; Carriero, G.; Tillmann, R.; Tomlinson, S. J.; Dragosits, U.; Gianelle, D.; Hewitt, C. N.; Nemitz, E.

    2015-10-01

    This paper reports the fluxes and mixing ratios of biogenically emitted volatile organic compounds (BVOCs) 4 m above a mixed oak and hornbeam forest in northern Italy. Fluxes of methanol, acetaldehyde, isoprene, methyl vinyl ketone + methacrolein, methyl ethyl ketone and monoterpenes were obtained using both a proton transfer reaction-mass spectrometer (PTR-MS) and a proton transfer reaction-time of flight-mass spectrometer (PTR-ToF-MS) together with the methods of virtual disjunct eddy covariance (PTR-MS) and eddy covariance (PTR-ToF-MS). Isoprene was the dominant emitted compound with a mean day-time flux of 1.9 mg m-2 h-1. Mixing ratios, recorded 4 m above the canopy, were dominated by methanol with a mean value of 6.2 ppbv over the 28 day measurement period. Comparison of isoprene fluxes calculated using the PTR-MS and PTR-ToF-MS showed very good agreement while comparison of the monoterpene fluxes suggested a slight over estimation of the flux by the PTR-MS. A basal isoprene emission rate for the forest of 1.7 mg m-2 h-1 was calculated using the MEGAN isoprene emissions algorithms (Guenther et al., 2006). A detailed tree species distribution map for the site enabled the leaf-level emissions of isoprene and monoterpenes recorded using GC-MS to be scaled up to produce a "bottom-up" canopy-scale flux. This was compared with the "top-down" canopy-scale flux obtained by measurements. For monoterpenes, the two estimates were closely correlated and this correlation improved when the plant species composition in the individual flux footprint was taken into account. However, the bottom-up approach significantly underestimated the isoprene flux, compared with the top-down measurements, suggesting that the leaf-level measurements were not representative of actual emission rates.

  16. Emission and Photochemical Evolution of Low Vapor Pressure-Volatile Organic Compounds (LVP-VOCs): from Consumer Products to Secondary Organic Aerosol

    NASA Astrophysics Data System (ADS)

    Li, L.; Kacarab, M.; Chen, C. L.; Price, D.; Carter, W. P. L.; Cocker, D. R., III

    2015-12-01

    Missing emission sources contribute to potential problems in air quality modeling and human health. Low Vapor Pressure-Volatile Organic Compounds (LVP-VOCs) are widely used in consumer products and currently receive VOC exemptions based on their vapor pressure. However, 58.5 TPD LVP-VOC is estimated to emit in 2020 from consumer products in California based on government and industry inventory data. This work investigates the emission and photochemical evolution of major LVP-VOCs in consumer products to demonstrate LVP-VOC impacts on criteria air pollutants. LVP-VOC emission potential is investigated by offline gravimetric and online headspace tracking pure compounds and consumer product mixtures under ambient relevant conditions. Only 3 of the 14 pure LVP-VOCs were found to be atmospherically unavailable. All target LVP-VOCs are observed to evaporate from tested consumer product mixtures. We found improved thermodynamic parameters to predict LVP-VOC evaporation rate. LVP-VOCs photochemical evolution and their impact on ozone and secondary organic aerosol (SOA) formation are evaluated by integrating SAPRC-11 modeling with laboratory studies in a 90 m3 dual environmental chamber at UC Riverside/CE-CERT. Simultaneous photooxidation experiments, with and without the LVP-VOC, are conducted in the presence of reactive organic gas (ROG) surrogate representing urban chemical smog. Further, LVP-VOC photochemical evolution pathway is investigated under various atmospheric activity (LVP + H2O2, LVP+NO or LVP+H2O2+NO) in the environmental chamber. Gas phase and particle phase mass spectrometers (SIFT-MS, Selected Ion Flow Tube-Mass Spectrum and HR-ToF-MS, High Resolution Time-of-Flight Aerosol mass Spectrometer) are applied to monitor the evolution of LVP-VOCs in the controlled atmosphere. The potential of LVP-VOC oxidation into ELVOC is also illustrated. We finally interpret the health risk and environmental concern related to LVP-VOC emission and photoxidation.

  17. Multivariate analysis of effects of diurnal temperature and seasonal humidity variations by tropical savanna climate on the emissions of anthropogenic volatile organic compounds.

    PubMed

    Liu, Chih-Chung; Chen, Wei-Hsiang; Yuan, Chung-Shin; Lin, Chitsan

    2014-02-01

    Volatile organic compounds (VOCs), particularly those from anthropogenic sources, have been of substantial concern. In this study, the influences of diurnal temperature and seasonal humidity variations by tropical savanna climate on the distributions of VOCs from stationary industrial sources were investigated by analyzing the concentrations during the daytime and nighttime in the dry and wet seasons and assessing the results by principal component analysis (PCA) and cluster analysis. Kaohsiung City in Southern Taiwan, known for its severe VOC pollution, was chosen as the location to be examined. In the results, the VOC concentrations were lower during the daytime and in the wet season, possibly attributed to the stronger photochemical reactions and increasing inhibition of VOC emissions and transports by elevating humidity levels. Certain compounds became appreciably more important at higher humidity, as these compounds were saturated hydrocarbons with relatively low molecular weights. The influence of diurnal temperature variation on VOC distribution behaviors seemed to be less important than and interacted with that of seasonal humidity variation. Heavier aromatic hydrocarbons with more complex structures and some aliphatic compounds were found to be the main species accounting for the maximum variances of the data observed at high humidity, and the distinct grouping of compounds implied a pronounced inherent characteristic of each cluster in the observed VOC distributions. Under the influence of diurnal temperature variation, selected VOCs that may have stronger photochemical resistances and/or longer lifetimes in the atmosphere were clustered with each other in the cluster analysis, whereas the other groups might consist of compounds with different levels of vulnerability to sunlight or high temperatures. These findings prove the complications in the current knowledge regarding the VOC contaminations and providing insight for managing the adverse impacts of

  18. Exposure to volatile organic compounds for individuals with occupations associated with potential exposure to motor vehicle exhaust and/or gasoline vapor emissions.

    PubMed

    Jo, W K; Song, K B

    2001-03-26

    Workers who work near volatile organic compounds (VOCs) source(s), motor vehicle exhausts and/or gasoline vapor emissions, are suspected to be exposed to highly-elevated VOC levels during their work-time. This study confirmed this suspicion and evaluated the work-time exposure VOCs for traffic police officers, parking garage attendants, service station attendants, roadside storekeepers and underground storekeepers, by measuring the concentrations of six aromatic VOCs in workplace air, or personal air and breath samples. For nearly all target VOCs, the post-work breath concentrations of the workers were slightly or significantly higher than the pre-work breath concentrations, depending on the compound and occupation. Furthermore, both the pre- and post-work breath concentrations of the workers showed elevated levels compared with a control group of college students. The post-work breath concentrations were significantly correlated with the personal air concentrations, while the pre-work breath concentrations were not. Smoking workers were not always exposed to higher aromatic VOC levels than non-smoking workers. The breath and personal air concentrations for all the target compounds were both higher for underground parking garage attendants than for ground-level parking attendants. For all the target compounds except toluene, storekeepers exhibited similar levels of exposure for all store types. Print shopkeepers recorded the highest toluene exposure.

  19. Opportunity Analysis for Recovering Energy from Industrial Waste Heat and Emissions

    SciTech Connect

    Viswanathan, Vish V.; Davies, Richard W.; Holbery, Jim D.

    2006-04-01

    United States industry consumed 32.5 Quads (34,300 PJ) of energy during 2003, which was 33.1% of total U.S. energy consumption (EIA 2003 Annual Energy Review). The U.S. industrial complex yields valuable goods and products. Through its manufacturing processes as well as its abundant energy consumption, it supports a multi-trillion dollar contribution to the gross domestic product and provides millions of jobs in the U.S. each year. Industry also yields waste products directly through its manufacturing processes and indirectly through its energy consumption. These waste products come in two forms, chemical and thermal. Both forms of waste have residual energy values that are not routinely recovered. Recovering and reusing these waste products may represent a significant opportunity to improve the energy efficiency of the U.S. industrial complex. This report was prepared for the U.S. Department of Energy Industrial Technologies Program (DOE-ITP). It analyzes the opportunity to recover chemical emissions and thermal emissions from U.S. industry. It also analyzes the barriers and pathways to more effectively capitalize on these opportunities. A primary part of this analysis was to characterize the quantity and energy value of the emissions. For example, in 2001, the industrial sector emitted 19% of the U.S. greenhouse gases (GHG) through its industrial processes and emitted 11% of GHG through electricity purchased from off-site utilities. Therefore, industry (not including agriculture) was directly and indirectly responsible for emitting 30% of the U.S. GHG. These emissions were mainly comprised of carbon dioxide (CO2), but also contained a wide-variety of CH4 (methane), CO (carbon monoxide), H2 (hydrogen), NMVOC (non-methane volatile organic compound), and other chemicals. As part of this study, we conducted a survey of publicly available literature to determine the amount of energy embedded in the emissions and to identify technology opportunities to capture and

  20. SIMULTANEOUS DETERMINATION OF ORGANOTIN, ORGANOLEAD, AND ORGANOMERCURY COMPOUNDS IN ENVIRONMENTAL SAMPLES USING CAPILLARY GAS CHROMATOGRAPHY WITH ATOMIC EMISSION DETECTION

    EPA Science Inventory

    As part of a continuing evaluation of new analytical and sample preparation techniques conducted by the US Environmental Protection Agency (EPA), the use of capillary gas chromatography with atomic emission detection (GC-AED) for the simultaneous determination of organotin, organ...

  1. Exhaust emissions from high speed passenger ferries

    NASA Astrophysics Data System (ADS)

    Cooper, D. A.

    Exhaust emission measurements have been carried out on-board three high-speed passenger ferries (A, B and C) during normal service routes. Ship A was powered by conventional, medium-speed, marine diesel engines, Ship B by gas turbine engines and Ship C conventional, medium-speed, marine diesel engines equipped with selective catalytic reduction (SCR) systems for NO x abatement. All ships had similar auxiliary engines (marine diesels) for generating electric power on-board. Real-world emission factors of NOx, SO2, CO, CO 2, NMVOC, CH4, N2O, NH3, PM and PAH at steady-state engine loads and for complete voyages were determined together with an estimate of annual emissions. In general, Ship B using gas turbines showed favourable NO x, PM and PAH emissions but at the expense of higher fuel consumption and CO 2 emissions. Ship C with the SCR had the lowest NO x emissions but highest NH 3 emissions especially during harbour approaches and stops. The greatest PM and PAH specific emissions were measured from auxiliary engines operating at low engine loads during harbour stops. Since all ships used a low-sulphur gas oil, SO 2 emissions were relatively low in all cases.

  2. A refined method for the calculation of the Non-Methane Volatile Organic Compound emission estimate from Domestic Solvent Usage in Ireland from 1992 to 2014 - A case study for Ireland

    NASA Astrophysics Data System (ADS)

    Barry, Stephen; O'Regan, Bernadette

    2016-08-01

    This study describes a new methodology to calculate Non-Methane Volatile Organic Compounds from Domestic Solvent Use including Fungicides over the period 1992-2014. Improved emissions data compiled at a much more refined level can help policy-makers develop more effective policy's to address environmental issues. However, a number of problems were found when member states attempt to use national statistics for Domestic Solvent Use including Fungicides. For instance, EMEP/EEA (2013) provides no guidance regarding which activity data should be used, resulting in emission estimates being potentially inconsistent and un-comparable. Also, previous methods and emission factors described in the EMEP/EEA (2013) guidebook do not exactly match data collected by state agencies. This makes using national statistics difficult. In addition, EMEP/EEA (2013) use broader categories than necessary (e.g. Cosmetics Aerosol/Non Aerosol) to estimate emissions while activity data is available at a more refined level scale (e.g. Personal Cleaning Products, Hair Products, Cosmetics, Deodorants and Perfumes). This can make identifying the drivers of emissions unclear. This study builds upon Tzanidakis et al. (2012) whereby it provides a method for collecting activity data from state statistics, developed country specific emission factors based on a survey of 177 Irish products and importantly, used a new method to account for the volatility of organic compounds found in commonly available domestic solvent containing products. This is the first study to account for volatility based on the characteristics of organic compounds and therefore is considered a more accurate method of accounting for emissions from this emission source. The results of this study can also be used to provide a simple method for other member parties to account for the volatility of organic compounds using sectorial adjustment factors described here. For comparison purposes, emission estimates were calculated using the

  3. CHARACTERIZATION OF LOW-VOC LATEX PAINTS: VOLATILE ORGANIC COMPOUND CONTENT, VOC AND ALDEHYDE EMISSIONS, AND PAINT PERFORMANCE

    EPA Science Inventory

    The report gives results of laboratory tests to evaluate commercially available latex paints advertised as "low-odor," "low-VOC (volatile organic compound)," or "no-VOC." Measurements were performed to quantify the total content of VOCs in the paints...

  4. USE OF BIOASSAY-DIRECTED CHEMICAL ANALYSIS FOR IDENTIFYING MUTAGENIC COMPOUNDS IN URBAN AIR AND COMBUSTION EMISSIONS

    EPA Science Inventory

    Bioassay-directed chemical analysis fractionation has been used for 30 years to identify mutagenic classes of compounds in complex mixtures. Most studies have used the Salmonella (Ames) mutagenicity assay, and we have recently applied this methodology to two standard reference sa...

  5. Response of fine particulate matter to emission changes of oxides of nitrogen and anthropogenic volatile organic compounds in the eastern United States

    SciTech Connect

    Alexandra P. Tsimpidi; Vlassis A. Karydis; Spyros N. Pandis

    2008-11-15

    A three-dimensional chemical transport model (Particulate Matter Comprehensive Air Quality Model with Extensions) is used to investigate changes in fine particle (PM2.5) concentrations in response to 50% emissions changes of oxides of nitrogen (NOx) and anthropogenic volatile organic compounds (VOCs) during July 2001 and January 2002 in the eastern United States. The reduction of NOx emissions by 50% during the summer results in lower average oxidant levels and lowers PM2.5 (8% on average), mainly because of reductions of sulfate (9-11%), nitrate (45-58%), and ammonium (7-11%). The organic particulate matter (PM) slightly decreases in rural areas, whereas it increases in cities by a few percent when NOx is reduced. Reduction of NOx during winter causes an increase of the oxidant levels and a rather complicated response of the PM components, leading to small net changes. Sulfate increases (8-17%), nitrate decreases (18-42%), organic PM slightly increases, and ammonium either increases or decreases a little. The reduction of VOC emissions during the summer causes on average a small increase of the oxidant levels and a marginal increase in PM2.5. This small net change is due to increases in the inorganic components and decreases of the organic ones. Reduction of VOC emissions during winter results in a decrease of the oxidant levels and a 5-10% reduction of PM2.5 because of reductions in nitrate (4-19%), ammonium (4-10%), organic PM (12-14%), and small reductions in sulfate. Although sulfur dioxide (SO{sub 2}) reduction is the single most effective approach for sulfate control, the coupled decrease of SO{sub 2} and NOx emissions in both seasons is more effective in reducing total PM2.5 mass than the SO{sub 2} reduction alone. 34 refs., 7 figs., 1 tab.

  6. Volatile organic compound emissions from the oil and natural gas industry in the Uinta Basin, Utah: point sources compared to ambient air composition

    NASA Astrophysics Data System (ADS)

    Warneke, C.; Geiger, F.; Edwards, P. M.; Dube, W.; Pétron, G.; Kofler, J.; Zahn, A.; Brown, S. S.; Graus, M.; Gilman, J.; Lerner, B.; Peischl, J.; Ryerson, T. B.; de Gouw, J. A.; Roberts, J. M.

    2014-05-01

    The emissions of volatile organic compounds (VOCs) associated with oil and natural gas production in the Uinta Basin, Utah were measured at a ground site in Horse Pool and from a NOAA mobile laboratory with PTR-MS instruments. The VOC compositions in the vicinity of individual gas and oil wells and other point sources such as evaporation ponds, compressor stations and injection wells are compared to the measurements at Horse Pool. High mixing ratios of aromatics, alkanes, cycloalkanes and methanol were observed for extended periods of time and short-term spikes caused by local point sources. The mixing ratios during the time the mobile laboratory spent on the well pads were averaged. High mixing ratios were found close to all point sources, but gas wells using dry-gas collection, which means dehydration happens at the well, were clearly associated with higher mixing ratios than other wells. Another large source was the flowback pond near a recently hydraulically re-fractured gas well. The comparison of the VOC composition of the emissions from the oil and natural gas wells showed that wet gas collection wells compared well with the majority of the data at Horse Pool and that oil wells compared well with the rest of the ground site data. Oil wells on average emit heavier compounds than gas wells. The mobile laboratory measurements confirm the results from an emissions inventory: the main VOC source categories from individual point sources are dehydrators, oil and condensate tank flashing and pneumatic devices and pumps. Raw natural gas is emitted from the pneumatic devices and pumps and heavier VOC mixes from the tank flashings.

  7. Canopy-scale flux measurements and bottom-up emission estimates of volatile organic compounds from a mixed oak and hornbeam forest in northern Italy

    NASA Astrophysics Data System (ADS)

    Acton, W. Joe F.; Schallhart, Simon; Langford, Ben; Valach, Amy; Rantala, Pekka; Fares, Silvano; Carriero, Giulia; Tillmann, Ralf; Tomlinson, Sam J.; Dragosits, Ulrike; Gianelle, Damiano; Hewitt, C. Nicholas; Nemitz, Eiko

    2016-06-01

    This paper reports the fluxes and mixing ratios of biogenically emitted volatile organic compounds (BVOCs) 4 m above a mixed oak and hornbeam forest in northern Italy. Fluxes of methanol, acetaldehyde, isoprene, methyl vinyl ketone + methacrolein, methyl ethyl ketone and monoterpenes were obtained using both a proton-transfer-reaction mass spectrometer (PTR-MS) and a proton-transfer-reaction time-of-flight mass spectrometer (PTR-ToF-MS) together with the methods of virtual disjunct eddy covariance (using PTR-MS) and eddy covariance (using PTR-ToF-MS). Isoprene was the dominant emitted compound with a mean daytime flux of 1.9 mg m-2 h-1. Mixing ratios, recorded 4 m above the canopy, were dominated by methanol with a mean value of 6.2 ppbv over the 28-day measurement period. Comparison of isoprene fluxes calculated using the PTR-MS and PTR-ToF-MS showed very good agreement while comparison of the monoterpene fluxes suggested a slight over estimation of the flux by the PTR-MS. A basal isoprene emission rate for the forest of 1.7 mg m-2 h-1 was calculated using the Model of Emissions of Gases and Aerosols from Nature (MEGAN) isoprene emission algorithms (Guenther et al., 2006). A detailed tree-species distribution map for the site enabled the leaf-level emission of isoprene and monoterpenes recorded using gas-chromatography mass spectrometry (GC-MS) to be scaled up to produce a bottom-up canopy-scale flux. This was compared with the top-down canopy-scale flux obtained by measurements. For monoterpenes, the two estimates were closely correlated and this correlation improved when the plant-species composition in the individual flux footprint was taken into account. However, the bottom-up approach significantly underestimated the isoprene flux, compared with the top-down measurements, suggesting that the leaf-level measurements were not representative of actual emission rates.

  8. Control of industrial VOC (volatile organic compound) emissions by catalytic incineration. volume 5. catalytic incinerator performance at industrial site c-3. Final report, May 1982-August 1983

    SciTech Connect

    Blacksmith, J.R.; Randall, J.L.

    1984-07-01

    The report is part of a two-phase EPA effort to assess the performance, suitability, and costs of various technologies to control emissions of volatile organic compounds (VOCs). In Phase 1, information was assembled from the literature on the use and cost of using catalytic incineration for VOC control. Results included: (1) a review of current and developing catalytic incineration technology, (2) an assessment of the overall performance of catalytic incinerators, (3) a review of applications where catalytic incinerators are used, (4) a comparative analysis of catalytic incineration with other competing VOC controls, (5) an examination of available methods for emission testing catalytic incinerators, and (6) an assessment of the need for additional performance test data. Phase 2 was a test program designed to increase the catalytic incinerator performance data base. It resulted in reports documenting the performance of eight catalytic incinerators at six industrial sites. The incinerators were used to control VOC emissions from solvent evaporation processes at can coating, coil coating, magnet wire, and graphic arts printing plants. Performance was measured at several process conditions at each site. Incinerator performance was characterized in terms of destruction efficiency, outlet solvent concentration, and energy usage. Design and operating data were collected. This report preseents test resultls and data evaluation for the testing conducted at the third test site, which involved the testing of two catalytic incinerators at Plant C-3, a graphic arts printing establishment.

  9. Emissions and ambient distributions of Biogenic Volatile Organic Compounds (BVOC) in a Ponderosa pine ecosystem: interpretation of PTR-MS mass spectra

    NASA Astrophysics Data System (ADS)

    Kim, S.; Karl, T.; Guenther, A.; Tyndall, G.; Orlando, J.; Harley, P.; Rasmussen, R.; Apel, E.

    2009-10-01

    Two proton-transfer-reaction mass spectrometry systems were deployed at the Bio-hydro-atmosphere interactions of Energy, Aerosols, Carbon, H2O, Organics and Nitrogen-Southern Rocky Mountain 2008 field campaign (BEACHON-SRM08; July to September 2008) at the Manitou Forest observatory in a Ponderosa pine woodland near Woodland Park, Colorado USA to simultaneously measure BVOC emissions and ambient distributions of their oxidation products. Here, we present mass spectral analysis in a wide range of masses (m/z=40+ to 210+) to assess our understanding of BVOC emissions and their photochemical process inside of the forest canopy. The biogenic terpenoids, 2-methyl-3-butene-2-ol (MBO, 50.2%) and several monoterpenes (MT, 33.5%) were identified as the dominant BVOC emissions from a transmission corrected mass spectrum, averaged over the daytime (11 am to 3 p.m., local time) of three days. To assess contributions of oxidation products of local BVOC, we calculate a oxidation product spectrum with the OH- and ozone-initiated oxidation product distribution mass spectra of two major BVOC at the ecosystem (MBO and β-pinene) that were observed from laboratory oxidation experiments. A majority (~73%) of the total signal could be ex