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Sample records for nitrogen dioxide no2

  1. Highly accurate nitrogen dioxide (NO2) in nitrogen standards based on permeation.

    PubMed

    Flores, Edgar; Viallon, Joële; Moussay, Philippe; Idrees, Faraz; Wielgosz, Robert Ian

    2012-12-01

    The development and operation of a highly accurate primary gas facility for the dynamic production of mixtures of nitrogen dioxide (NO(2)) in nitrogen (N(2)) based on continuous weighing of a permeation tube and accurate impurity quantification and correction of the gas mixtures using Fourier transform infrared spectroscopy (FT-IR) is described. NO(2) gas mixtures in the range of 5 μmol mol(-1) to 15 μmol mol(-1) with a standard relative uncertainty of 0.4% can be produced with this facility. To achieve an uncertainty at this level, significant efforts were made to reduce, identify and quantify potential impurities present in the gas mixtures, such as nitric acid (HNO(3)). A complete uncertainty budget, based on the analysis of the performance of the facility, including the use of a FT-IR spectrometer and a nondispersive UV analyzer as analytical techniques, is presented in this work. The mixtures produced by this facility were validated and then selected to provide reference values for an international comparison of the Consultative Committee for Amount of Substance (CCQM), number CCQM-K74, (1) which was designed to evaluate the consistency of primary NO(2) gas standards from 17 National Metrology Institutes. PMID:23148702

  2. Nitrogen dioxide (NO2) uptake by vegetation controlled by atmospheric concentrations and plant stomatal aperture

    NASA Astrophysics Data System (ADS)

    Chaparro-Suarez, I. G.; Meixner, F. X.; Kesselmeier, J.

    2011-10-01

    Nitrogen dioxide (NO2) exchange between the atmosphere and five European tree species was investigated in the laboratory using a dynamic branch enclosure system (consisting of two cuvettes) and a highly specific NO2 analyzer. NO2 measurements were performed with a sensitive gas phase chemiluminescence NO detector combined with a NO2 specific (photolytic) converter, both from Eco-Physics (Switzerland). This highly specific detection system excluded bias from other nitrogen compounds. Investigations were performed at two light intensities (Photosynthetic Active Radiation, PAR, 450 and 900 μmol m-2 s-1) and NO2 concentrations between 0 and 5 ppb. Ambient parameters (air temperature and relative humidity) were held constant. The data showed dominant NO2 uptake by the respective tree species under all conditions. The results did not confirm the existence of a compensation point within a 95% confidence level, though we cannot completely exclude emission of NO2 under very low atmospheric concentrations. Induced stomatal stricture, or total closure, by changing light conditions, as well as by application of the plant hormone ABA (Abscisic Acid) caused a corresponding decrease of NO2 uptake. No loss of NO2 to plant surfaces was observed under stomatal closure and species dependent differences in uptake rates could be clearly related to stomatal behavior.

  3. Improved retrieval of nitrogen dioxide (NO2) column densities by means of MKIV Brewer spectrophotometers

    NASA Astrophysics Data System (ADS)

    Diémoz, H.; Siani, A. M.; Redondas, A.; Savastiouk, V.; McElroy, C. T.; Navarro-Comas, M.; Hase, F.

    2014-11-01

    A new algorithm to retrieve nitrogen dioxide (NO2) column densities using MKIV ("Mark IV") Brewer spectrophotometers is described. The method includes several improvements, such as a more recent spectroscopic data set, the reduction of measurement noise, interference by other atmospheric species and instrumental settings, and a better determination of the zenith sky air mass factor. The technique was tested during an ad hoc calibration campaign at the high-altitude site of Izaña (Tenerife, Spain) and the results of the direct sun and zenith sky geometries were compared to those obtained by two reference instruments from the Network for the Detection of Atmospheric Composition Change (NDACC): a Fourier Transform Infrared Radiometer (FTIR) and an advanced visible spectrograph (RASAS-II) based on the differential optical absorption spectrometry (DOAS) technique. To determine the extraterrestrial constant, an easily implementable extension of the standard Langley technique for very clean sites without tropospheric NO2 was developed which takes into account the daytime linear drift of stratospheric nitrogen dioxide due to photochemistry. The measurement uncertainty was thoroughly determined by using a Monte Carlo technique. Poisson noise and wavelength misalignments were found to be the most influential contributors to the overall uncertainty, and possible solutions are proposed for future improvements. The new algorithm is backward-compatible, thus allowing for the reprocessing of historical data sets.

  4. On the Hydrophobicity of Nitrogen Dioxide: Could there be a “lens” effect for NO2 reaction kinetics?

    PubMed Central

    Squadrito, Giuseppe L.; Postlethwait, Edward M.

    2009-01-01

    Solvent “lens” effects for the reaction kinetics of NO2 can be evaluated on the basis of published Henry’s law constants for nitrogen dioxide in various solvents. Water-to-organic solvent partition coefficients were derived from Henry’s law constants and used to assess the tendencies of NO2 toward fleeing the aqueous environments and concentrating in biological hydrophobic media. It is concluded, based only on the estimated aqueous medium-to-cell membrane partition coefficient for NO2, that such tendencies will be relatively small, and that they may account for an acceleration of chemical reactions in biological hydrophobic media with reaction kinetics that are first order on NO2 by a factor of approximately 3 ± 1. Thus, kinetic effects due to mass action will be relatively small but it is also important to recognize that because NO2 will tend to dissolve in cell membranes, reactions with cell membrane components will not be hindered by lack of physical solubility at these loci. In comparison to other gases, nitrogen dioxide is less hydrophobic than NO, O2 and N2. PMID:19540354

  5. The economic benefits of reducing the levels of nitrogen dioxide (NO2) near primary schools: The case of London.

    PubMed

    Guerriero, Carla; Chatzidiakou, Lia; Cairns, John; Mumovic, Dejan

    2016-10-01

    Providing a healthy school environment is a priority for child health. The aim of this study is to develop a methodology that allows quantification of the potential economic benefit of reducing indoor exposure to nitrogen dioxide (NO2) in children attending primary schools. Using environmental and health data collected in primary schools in London, this study estimates that, on average, 82 asthma exacerbations per school can be averted each year by reducing outdoor NO2 concentrations. The study expands upon previous analyses in two ways: first it assesses the health benefits of reducing children's exposure to indoor NO2 while at school, second it considers the children's perspective in the economic evaluation. Using a willingness to pay approach, the study quantifies that the monetary benefits of reducing children's indoor NO2 exposure while at school would range between £2.5 k per school if a child's perspective based on child's budget is adopted up to £60 k if a parent's perspective is considered. This study highlights that designers, engineers, policymakers and stakeholders need to consider the reduction of outdoor pollution, and particularly NO2 levels, near primary schools as there may be substantial health and monetary benefits. PMID:27451292

  6. 77 FR 9532 - Air Quality Designations for the 2010 Primary Nitrogen Dioxide (NO2

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-02-17

    ... Illinois, Indiana, Michigan, Branch, EPA Region 5, 77 West Jackson Minnesota, Ohio, and Street, Chicago, IL... Agency FR Federal Register FRM Federal Reference Method NAAQS National Ambient Air Quality Standards NO 2... component of greatest concern and is used as the indicator for the larger group of NO X . (See 75 FR...

  7. Nitrogen dioxide

    Integrated Risk Information System (IRIS)

    Nitrogen dioxide ; CASRN 10102 - 44 - 0 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogeni

  8. Nitrogen dioxide detection

    DOEpatents

    Sinha, Dipen N.; Agnew, Stephen F.; Christensen, William H.

    1993-01-01

    Method and apparatus for detecting the presence of gaseous nitrogen dioxide and determining the amount of gas which is present. Though polystyrene is normally an insulator, it becomes electrically conductive in the presence of nitrogen dioxide. Conductance or resistance of a polystyrene sensing element is related to the concentration of nitrogen dioxide at the sensing element.

  9. New High-Resolution Analysis of the 3ν 3 and 2ν 1 + ν 3 Bands of Nitrogen Dioxide (NO 2) by Fourier Transform Spectroscopy

    NASA Astrophysics Data System (ADS)

    Stephen, T. M.; Goldman, A.; Perrin, A.; Flaud, J.-M.; Keller, F.; Rinsland, C. P.

    2000-05-01

    Using new high-resolution Fourier transform spectra recorded at the University of Denver in the 2-μm region, a new and more extended analysis of the 2ν1 + ν3 and 3ν3 bands of nitrogen dioxide, located at 4179.9374 and 4754.2039 cm-1, respectively, has been performed. The spin-rotation energy levels were satisfactorily reproduced using a theoretical model that takes into account both the Coriolis interactions between the spin-rotation energy levels of the (201) vibrational 'bright' state with those of the (220) 'dark' state. The interactions between the (003) bright state with the (022) dark state were similarly treated. The spin-rotation resonances within each of the NO2 vibrational states were also taken into account. The precise vibrational energies and the rotational, spin-rotational, and coupling constants were obtained for the two dyads {(220), (201)} and {(022), (003)} of the 14N16O2 interacting states. From the experimental line intensities of the 2ν1 + ν3 and 3ν3 bands, a determination of their vibrational transition moment constants was performed. A comprehensive list of line positions and line intensities of the {2ν1 + 2ν2, 2ν1 + ν3} and the {2ν2 + 2ν3, 3ν3} interacting bands of 14N16O2 was generated. In addition, assuming the harmonic approximation and using the Hamiltonian constants derived in this work and in previous studies (A. Perrin, J.-M. Flaud, A. Goldman, C. Camy-Peyret, W. J. Lafferty, Ph. Arcas, and C. P. Rinsland, J. Quant. Spectrosc. Radiat. Transfer 60, 839-850 (1998)), we have generated synthetic spectra for the {(022), (003)}-{(040), (021), (002)} hot bands at 6.3 μm and for the {(220), (201)}-{(100), (020), (001)} hot bands at 3.5 μm, which are in good agreement with the observed spectra.

  10. Accurate Fourier transform infrared (FT-IR) spectroscopy measurements of nitrogen dioxide (NO2) and nitric acid (HNO3) calibrated with synthetic spectra.

    PubMed

    Flores, Edgar; Viallon, Joële; Moussay, Philippe; Wielgosz, Robert Ian

    2013-10-01

    A novel method for determining the accuracy of laboratory-based measurements of nitrogen dioxide (NO2) and nitric acid (HNO3) mole fractions using Fourier transform infrared (FT-IR) spectroscopy 1 cm(-1) resolution instruments calibrated with synthetic spectra has been developed. The traceability of these measurement results is to the reference line strength data contained within the high-resolution transmission molecular absorption (HITRAN) database. Incorporating a proper estimate of the uncertainty of this data into the measurement results will ensure that the SI traceable values are encompassed within the uncertainty of the measurement results. The major contributors to the uncertainties of the results are, in descending order of importance, the uncertainty in the line strength values (HITRAN 2004), the uncertainty attributed to the generation of reference spectra (including knowledge of the optical path length of the FT-IR gas cell), and temperature measurements of the gas. The stability of the FT-IR instrument itself is only a minor contributor to the overall uncertainty of the measurements. FT-IR measurements of NO2 mole fractions at nominal values of 10 μmol mol(-1) calibrated with synthetic spectra lead to standard uncertainties of 0.34 μmol mol(-1) (3.4% relative). In contrast, calibration of the FT-IR instrument with SI traceable gas standards generated by a dynamic weighing system resulted in measurements results with standard uncertainties of 0.04 μmol mol(-1) (0.4% relative). When comparing the consistency of measurement results based on the synthetic calibration method against those obtained by calibrations with SI traceable gas standards, the existence of a potential bias of ~5% was observed, although this was within the stated uncertainties of the results. The FT-IR measurements of HNO3 mole fractions at nominal values of 200 nmol mol(-1) calibrated with synthetic spectra resulted in values with standard uncertainties of 23 nmol mol(-1) (11

  11. PERSONAL MONITOR FOR NITROGEN DIOXIDE

    EPA Science Inventory

    An attempt was made to develop a personal monitor to measure nitrogen dioxide. Sampling of nitrogen dioxide is accomplished by permeation through a silicone membrane into a alkaline thymol blue solution. The nitrogen dioxide is converted to nitrite and is then quantitated by colo...

  12. Estimated global nitrogen deposition using NO2 column density

    USGS Publications Warehouse

    Lu, Xuehe; Jiang, Hong; Zhang, Xiuying; Liu, Jinxun; Zhang, Zhen; Jin, Jiaxin; Wang, Ying; Xu, Jianhui; Cheng, Miaomiao

    2013-01-01

    Global nitrogen deposition has increased over the past 100 years. Monitoring and simulation studies of nitrogen deposition have evaluated nitrogen deposition at both the global and regional scale. With the development of remote-sensing instruments, tropospheric NO2 column density retrieved from Global Ozone Monitoring Experiment (GOME) and Scanning Imaging Absorption Spectrometer for Atmospheric Chartography (SCIAMACHY) sensors now provides us with a new opportunity to understand changes in reactive nitrogen in the atmosphere. The concentration of NO2 in the atmosphere has a significant effect on atmospheric nitrogen deposition. According to the general nitrogen deposition calculation method, we use the principal component regression method to evaluate global nitrogen deposition based on global NO2 column density and meteorological data. From the accuracy of the simulation, about 70% of the land area of the Earth passed a significance test of regression. In addition, NO2 column density has a significant influence on regression results over 44% of global land. The simulated results show that global average nitrogen deposition was 0.34 g m−2 yr−1 from 1996 to 2009 and is increasing at about 1% per year. Our simulated results show that China, Europe, and the USA are the three hotspots of nitrogen deposition according to previous research findings. In this study, Southern Asia was found to be another hotspot of nitrogen deposition (about 1.58 g m−2 yr−1 and maintaining a high growth rate). As nitrogen deposition increases, the number of regions threatened by high nitrogen deposits is also increasing. With N emissions continuing to increase in the future, areas whose ecosystem is affected by high level nitrogen deposition will increase.

  13. The development of a nitrogen dioxide sonde

    NASA Astrophysics Data System (ADS)

    Sluis, W. W.; Allaart, M. A. F.; Piters, A. J. M.; Gast, L. F. L.

    2010-12-01

    A growing number of space-borne instruments measures nitrogen dioxide (NO2) concentrations in the troposphere, but validation of these instruments is hampered by the lack of ground-based and in situ profile measurements. The Royal Netherlands Meteorological Institute (KNMI) has developed a working NO2 sonde. The sonde is attached to a small meteorological balloon and measures a tropospheric NO2 profile. The NO2 sonde has a vertical resolution of 5 m and a measurement range between 1 and 100 ppbv. The instrument is light in weight (0.7 kg), cheap (disposable), energy efficient and not harmful to the environment or the person who finds the package after use. The sonde uses the chemiluminescent reaction of NO2 in an aqueous luminol solution. The NO2-luminol reaction produces faint blue/purple light (at about 425 nm), which is detected by an array of silicon photodiodes. The luminol solution is optimised to be specific to NO2. An on-ground comparison with measurements from a Photolytic Analyser of The National Institute for Public Health and the Environment (RIVM) shows that both instruments measure similar NO2 variations in ambient air. During the Cabauw Intercomparison campaign of Nitrogen Dioxide measuring instruments (CINDI) in June/July 2009, six vertical profiles of NO2 from the ground to a 5 km altitude were measured, which clearly show that the largest amount of NO2 is measured in the boundary layer. The measured boundary layer heights of the NO2 sonde are in good agreement with boundary layer heights determined by a LD40 Ceilometer at Cabauw.

  14. Ambient Pressure LIF Instrument for Nitrogen Dioxide

    NASA Astrophysics Data System (ADS)

    Parra, J.; George, L. A.

    2009-12-01

    Concerns about the health effects of nitrogen dioxide (NO2) and its role in forming deleterious atmospheric species have made it desirable to have low-cost, sensitive ambient measurements of NO2. A continuous-wave laser-diode Laser Induced Fluorescence (LIF) system for NO2 that operates at ambient pressure has been developed, thereby eliminating the need for an expensive pumping system. The use of high quality optical filters has facilitated low-concentration detection of NO2 using atmospheric pressure LIF by providing substantial discrimination against scattered laser photons without the use of time-gated electronics, which add complexity and cost to the LIF instrumentation. This improvement allows operation at atmospheric pressure with a low-cost diaphragm sampling pump. The current prototype system has achieved sensitivity several orders of magnitude beyond previous efforts at ambient pressure (LOD of 2 ppb, 60 s averaging time). Ambient measurements of NO2 were made in Portland, OR using both the standard NO2 chemiluminescence method (CL-NO2) and the LIF instrument and showed good agreement (r2 = 0.92). Our instrument is currently being developed as a “back-end” detector for a more field portable NOy system. In addition, we are currently utilizing this instrument to study surface chemistry involving NO2 at atmospherically relevant concentrations and pressures.

  15. TECHNICAL ASSISTANCE DOCUMENT FOR THE CHEMILUMINESCENCE MEASUREMENT OF NITROGEN DIOXIDE

    EPA Science Inventory

    Gas phase chemiluminescence has been designated as the reference measurement principle for the measurement of nitrogen dioxide (NO2) in the ambient atmosphere. Continuous analyzers based on this measurement principle may be calibrated with NO2 either from the gas phase titration ...

  16. The Development of a Nitrogen Dioxide Sonde

    NASA Astrophysics Data System (ADS)

    Sluis, Wesley; Allaart, Marc; Piters, Ankie; Gast, Lou

    2010-05-01

    Nitrogen dioxide is an important pollutant in the atmosphere, it is toxic for living species, it forms photochemical tropospheric ozone, and acid rain. There is a growing number of space-borne instruments to measure nitrogen dioxide concentrations in the atmosphere, but validation of these instruments is hampered by lack of ground-based and in-situ profile measurements. The Royal Netherlands Meteorological Institute (KNMI) has developed a working NO2 sonde. The sonde is attached to a small meteorological balloon and measures a tropospheric NO2 profile. The NO2 sonde has a vertical resolution of 5 meter, and a measurement range between 1 and 100 ppbv. The instrument is light in weight (±300 gram), cheap (disposable), energy efficient and not harmful to the environment or the person who finds the package after use. Therefore the popular molybdenum catalytic converter or a photomultiplier tube can not be used. Instead the sonde uses the chemiluminescent reaction of NO2 in an aqueous luminol solution. The NO2- luminol reaction produces a faint blue/purple light (± 425 nm), which is detected by an array of silicon photodiodes. The instrument is equipped with a reservoir filled with luminol solution. A small piezoelectric diaphragm pump, pumps the luminol solution into a reaction vessel. A Teflon air pump forces the ambient air into the reaction vessel. The NO2 in the ambient air reacts with the luminol solution, and the emitted light is detected by an array of silicon photodiodes which are mounted on the reaction vessel. The generated current in the photodiodes is amplified and relayed to the ground by a Vaisala (RS92) radiosonde. The reaction vessel and the amplifiers are mounted in a tin can, to shield against electrostatic and radio interference, and stray light. All the air tubes used for the instrument are made of Teflon. The luminol solution is optimised to be specific to NO2. Sodium sulphate, sodium EDTA and Triton X-100 are added to the luminol solution to

  17. Nitrogen dioxide and respiratory illnesses in infants

    SciTech Connect

    Samet, J.M.; Lambert, W.E.; Skipper, B.J.; Cushing, A.H.; Hunt, W.C.; Young, S.A.; McLaren, L.C.; Schwab, M.; Spengler, J.D. )

    1993-11-01

    Nitrogen dioxide is an oxidant gas that contaminates outdoor air and indoor air in homes with unvented gas appliances. A prospective cohort study was carried out to test the hypothesis that residential exposure to NO2 increases incidence and severity of respiratory illnesses during the first 18 months of life. A cohort of 1,205 healthy infants from homes without smokers was enrolled. The daily occurrence of respiratory symptoms and illnesses was reported by the mothers every 2 wk. Illnesses with wheezing or wet cough were classified as lower respiratory tract. Indoor NO2 concentrations were serially measured with passive samplers place in the subjects' bedrooms. In stratified analyses, illness incidence rates did not consistently increase with exposure to NO2 or stove type. In multivariate analyses that adjusted for potential confounding factors, odds ratios were not significantly elevated for current or lagged NO2 exposures, or stove type. Illness duration, a measure of illness severity, was not associated with NO2 exposure. The findings can be extended to homes with gas stoves in regions of the United States where the outdoor air is not heavily polluted by NO2.

  18. SAGE observations of stratospheric nitrogen dioxide

    NASA Technical Reports Server (NTRS)

    Chu, W. P.; Mccormick, M. P.

    1986-01-01

    The global distribution of nitrogen dioxide in the middle to upper stratosphere (25-45 km altitude) for the period February 1979 to November 1981 has been determined from observations of attenuated solar radiation in the visible region 0.385-0.45 micron by the Stratospheric Aerosol and Gas Experiment (SAGE) satellite instrument. The SAGE-derived NO2 vertical profiles compare well with observations by balloon- and aircraft-borne sensors. The global SAGE NO2 distributions generally show a maximum in mixing ratio of 8 parts per billion by volume at about 35 km altitude near the equatorial latitudes at local sunset. The location of the mixing ratio peak moves synchronously with the overhead sun for the four different seasons. High-latitude NO2 column content shows strong seasonal variation, with a maximum in local summer and a minimum in local winter. Selected data at high-latitude winter seasons are presented, suggesting that the large variation shown could be explained by the coupling of both dynamics and photochemistry of the NO(x) species. Finally, profiles of the ratio of sunset to sunrise NO2 mixing ratios, peaking at about a factor of two at 30 km, are shown.

  19. NITROGEN DIOXIDE PHOTOLYTIC, RADIOMETRIC, AND METEOROLOGICAL FIELD DATA

    EPA Science Inventory

    Photolysis of nitrogen dioxide is a major reaction resulting in the formation of ozone in the troposphere. The rate constant, k1, for the photodissociation of NO2 is, under ambient conditions, a function of latitude, solar zenith angle, and cloud cover; therefore, k1 is highly va...

  20. EFFECTS OF NITROGEN DIOXIDE ON PULMONARY FUNCTION IN HUMAN SUBJECTS

    EPA Science Inventory

    Twenty human subjects with asthma and chronic bronchitis and ten normal, healthy adults were exposed to 0.5 ppm of nitrogen dioxide (NO2) for two hours in an environmental chamber. They engaged in one 15-minute, light to medium-exercise stint on a bicycle ergometer during this pe...

  1. INFLUENCE OF NITROGEN DIOXIDE ON XENOBIOTIC METABOLISM IN ANIMALS

    EPA Science Inventory

    Potential extrapulmonary effects of nitrogen dioxide (NO2) on hepatic xenobiotic metabolism were examined. Initial studies were conducted using pentobarbital (PEN) induced sleeping time (S.T.) in mice as an indicator of integrated mechanisms of xenobiotic clearance. A 3 hr. expos...

  2. A land use regression application into assessing spatial variation of intra-urban fine particulate matter (PM2.5) and nitrogen dioxide (NO2) concentrations in City of Shanghai, China.

    PubMed

    Liu, Chao; Henderson, Barron H; Wang, Dongfang; Yang, Xinyuan; Peng, Zhong-Ren

    2016-09-15

    Intra-urban assessment of air pollution exposure has become a priority study while international attention was attracted to PM2.5 pollution in China in recent years. Land Use Regression (LUR), which has previously been proved to be a feasible way to describe the relationship between land use and air pollution level in European and American cities, was employed in this paper to explain the correlations and spatial variations in Shanghai, China. PM2.5 and NO2 concentrations at 35-45 monitoring locations were selected as dependent variables, and a total of 44 built environmental factors were extracted as independent variables. Only five factors showed significant explanatory value for both PM2.5 and NO2 models: longitude, distance from monitors to the ocean, highway intensity, waterbody area, and industrial land area for PM2.5 model; residential area, distance to the coast, industrial area, urban district, and highway intensity for NO2 model. Respectively, both PM2.5 and NO2 showed anti-correlation with coastal proximity (an indicator of clean air dilution) and correlation with highway and industrial intensity (source indicators). NO2 also showed significant correlation with local indicators of population density (residential intensity and urban classification), while PM2.5 showed significant correlation with regional dilution (longitude as a indicator of distance from polluted neighbors and local water features). Both adjusted R squared values were strong with PM2.5 (0.88) being higher than NO2 (0.62). The LUR was then used to produce continuous concentration fields for NO2 and PM2.5 to illustrate the features and, potentially, for use by future studies. Comparison to PM2.5 studies in New York and Beijing show that Shanghai PM2.5 pollutant distribution was more sensitive to geographic location and proximity to neighboring regions. PMID:27203521

  3. High resolution nitrogen dioxide observations: retrieval, evaluation, and interpretation

    NASA Astrophysics Data System (ADS)

    Lamsal, L. N.; Janz, S. J.; Krotkov, N. A.; Pickering, K. E.; Kowalewski, M. G.; Loughner, C.; Spurr, R. J. D.; Crawford, J. H.

    2015-12-01

    The Airborne Compact Atmospheric Mapper (ACAM) deployed during the DISCOVER-AQ Maryland field campaign made hyperspectral remote sensing measurements in the 304-910 nm range allowing observations of several tropospheric pollutants including nitrogen dioxide (NO2) at an unprecedented spatial resolution of 1.5x0.75 km2. We apply the DOAS method, include high resolution information for surface reflectivity and vertical distributions of NO2 and aerosols, and account for temporal variation in atmospheric NO2 to retrieve lower tropospheric NO2 column. We compare NO2 from ACAM with observations from in-situ aircraft, ground-based PANDORA, and space-based OMI, and NO2 simulation from air quality models. The high resolution ACAM measurements offer not only new insights into our understanding of atmospheric composition and chemistry through observation of sub-sampling variability in typical satellite and model resolutions, but also opportunities for algorithm improvements for upcoming geostationary air quality missions.

  4. Atmospheric NH3 and NO2 concentration and nitrogen deposition in an agricultural catchment of Eastern China.

    PubMed

    Yang, Rong; Hayashi, Kentaro; Zhu, Bin; Li, Feiyue; Yan, Xiaoyuan

    2010-09-15

    To assess the atmospheric environmental impacts of anthropogenic reactive nitrogen in the fast-developing Eastern China region, we measured atmospheric concentrations of nitrogen dioxide (NO(2)) and ammonia (NH(3)) as well as the wet deposition of inorganic nitrogen (NO(3)(-) and NH(4)(+)) and dissolved organic nitrogen (DON) levels in a typical agricultural catchment in Jiangsu Province, China, from October 2007 to September 2008(.) The annual average gaseous concentrations of NO(2) and NH(3) were 42.2 microg m(-3) and 4.5 microg m(-3) (0 degree C, 760 mm Hg), respectively, whereas those of NO(3)(-), NH(4)(+), and DON in the rainwater within the study catchment were 1.3, 1.3, and 0.5 mg N L(-1), respectively. No clear difference in gaseous NO(2) concentrations and nitrogen concentrations in collected rainwater was found between the crop field and residential sites, but the average NH(3) concentration of 5.4 microg m(-3) in residential sites was significantly higher than that in field sites (4.1 microg m(-3)). Total depositions were 40 kg N ha(-1) yr(-1) for crop field sites and 30 kg N ha(-1) yr(-1) for residential sites, in which dry depositions (NO(2) and NH(3)) were 7.6 kg N ha(-1) yr(-1) for crop field sites and 1.9 kg N ha(-1) yr(-1) for residential sites. The DON in the rainwater accounted for 16% of the total wet nitrogen deposition. Oxidized N (NO(3)(-) in the precipitation and gaseous NO(2)) was the dominant form of nitrogen deposition in the studied region, indicating that reactive forms of nitrogen created from urban areas contribute greatly to N deposition in the rural area evaluated in this study. PMID:20624633

  5. Ozone and nitrogen dioxide above the northern Tien Shan

    NASA Technical Reports Server (NTRS)

    Arefev, Vladimir N.; Volkovitsky, Oleg A.; Kamenogradsky, Nikita E.; Semyonov, Vladimir K.; Sinyakov, Valery P.

    1994-01-01

    The results of systematic perennial measurements of the total ozone (since 1979) and nitrogen dioxide column (since 1983) in the atmosphere in the European-Asian continent center above the mountainmass of the Tien Shan are given. This region is distinguished by a great number of sunny days during a year. The observation station is at the Northern shore of Issyk Kul Lake (42.56 N 77.04 E 1650 m above the sea level). The measurement results are presented as the monthly averaged atmospheric total ozone and NO2 stratospheric column abundances (morning and evening). The peculiarities of seasonal variations of ozone and nitrogen dioxide atmospheric contents, their regular variances with a quasi-biennial cycles and trends have been noticed. Irregular variances of ozone and nitrogen dioxide atmospheric contents, i.e. their positive and negative anomalies in the monthly averaged contents relative to the perennial averaged monthly means, have been analyzed. The synchronous and opposite in phase anomalies in variations of ozone and nitrogen dioxide atmospheric contents were explained by the transport and zonal circulation in the stratosphere (Kamenogradsky et al., 1990).

  6. Leaf nitrogen dioxide uptake coupling apoplastic chemistry, carbon/sulfur assimilation, and plant nitrogen status.

    PubMed

    Hu, Yanbo; Sun, Guangyu

    2010-10-01

    Emission and plant uptake of atmospheric nitrogen oxides (NO + NO(2)) significantly influence regional climate change by regulating the oxidative chemistry of the lower atmosphere, species composition and the recycling of carbon and nutrients, etc. Plant uptake of nitrogen dioxide (NO(2)) is concentration-dependent and species-specific, and covaries with environmental factors. An important factor determining NO(2) influx into leaves is the replenishment of the substomatal cavity. The apoplastic chemistry of the substomatal cavity plays crucial roles in NO(2) deposition rates and the tolerance to NO(2), involving the reactions between NO(2) and apoplastic antioxidants, NO(2)-responsive germin-like proteins, apoplastic acidification, and nitrite-dependent NO synthesis, etc. Moreover, leaf apoplast is a favorable site for the colonization by microbes, which disturbs nitrogen metabolism of host plants. For most plant species, NO(2) assimilation in a leaf primarily depends on the nitrate (NO(3) (-)) assimilation pathway. NO(2)-N assimilation is coupled with carbon and sulfur (sulfate and SO(2)) assimilation as indicated by the mutual needs for metabolic intermediates (or metabolites) and the NO(2)-caused changes of key metabolic enzymes such as phosphoenolpyruvate carboxylase (PEPc) and adenosine 5'-phosphosulfate sulfotransferase, organic acids, and photorespiration. Moreover, arbuscular mycorrhizal (AM) colonization improves the tolerance of host plants to NO(2) by enhancing the efficiency of nutrient absorption and translocation and influencing foliar chemistry. Further progress is proposed to gain a better understanding of the coordination between NO(2)-N, S and C assimilation, especially the investigation of metabolic checkpoints, and the effects of photorespiratory nitrogen cycle, diverse PEPc and the metabolites such as cysteine, O-acetylserine (OAS) and glutathione. PMID:20628880

  7. NITROGEN DIOXIDE AND RESPIRATORY ILLNESS IN CHILDREN

    EPA Science Inventory

    Drs. Jonathan M. Samet, John D. Spengler, and colleagues conducted a prospective investigation of 1,205 health infants living in homes with gas or electric stoves in Albuquerque, NM. Nitrogen dioxide exposures were carefully estimated from repeated measurements in multiple ...

  8. NITROGEN DIOXIDE EXPOSURE AND LUNG ANTIOXIDANTS IN ASCORBIC ACID-DEFICIENT GUINEA PIGS

    EPA Science Inventory

    The authors have previously found that ascorbic acid (AA) deficiency in guinea pigs enhances the pulmonary toxicity of nitrogen dioxide (NO2). The present study showed that exposure to NO2 (4.8 ppm, 3 hr) significantly increased lung lavage fluid protein (a sensitive indicator of...

  9. Ambient intercomparison of direct and indirect methods for ambient nitrogen dioxide

    EPA Science Inventory

    AbstractRecent advances in measurement techniques for nitrogen dioxide (NO2), along with known interferences in the current Federal Reference Method (FRM) have created the need for NO2 measurement method research within EPA’s Office of Research and Development. Current meth...

  10. HEALTH EFFECTS OF SHORT-TERM INHALATION OF NITROGEN DIOXIDE AND OZONE MIXTURES

    EPA Science Inventory

    The effects of single and multiple daily 3-hour exposures to nitrogen dioxide (NO2) and ozone (O3) mixtures on the resistance to streptococcal pneumonia were investigated. The concentrations of NO2 ranged from 1.5 to 5.0 ppm, and those of O3, from 0.05 to 0.5 ppm. The effect of a...

  11. EFFECTS OF 0.1 PPM NITROGEN DIOXIDE ON AIRWAYS OF NORMAL AND ASTHMATIC SUBJECTS

    EPA Science Inventory

    It has been reported that inhalation of nitrogen dioxide (NO2) will enhance the bronchial reactivity of asthmatics. This study was designed to evaluate the respiratory effect of a 1-h exposure of normal subjects and of atopic asthmatics to 0.1 parts per million (ppm) NO2. Fifteen...

  12. 21 CFR 868.2385 - Nitrogen dioxide analyzer.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 8 2011-04-01 2011-04-01 false Nitrogen dioxide analyzer. 868.2385 Section 868...) MEDICAL DEVICES ANESTHESIOLOGY DEVICES Monitoring Devices § 868.2385 Nitrogen dioxide analyzer. (a) Identification. The nitrogen dioxide analyzer is a device intended to measure the concentration of...

  13. 21 CFR 868.2385 - Nitrogen dioxide analyzer.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 8 2013-04-01 2013-04-01 false Nitrogen dioxide analyzer. 868.2385 Section 868...) MEDICAL DEVICES ANESTHESIOLOGY DEVICES Monitoring Devices § 868.2385 Nitrogen dioxide analyzer. (a) Identification. The nitrogen dioxide analyzer is a device intended to measure the concentration of...

  14. 21 CFR 868.2385 - Nitrogen dioxide analyzer.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Nitrogen dioxide analyzer. 868.2385 Section 868...) MEDICAL DEVICES ANESTHESIOLOGY DEVICES Monitoring Devices § 868.2385 Nitrogen dioxide analyzer. (a) Identification. The nitrogen dioxide analyzer is a device intended to measure the concentration of...

  15. 21 CFR 868.2385 - Nitrogen dioxide analyzer.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 8 2014-04-01 2014-04-01 false Nitrogen dioxide analyzer. 868.2385 Section 868...) MEDICAL DEVICES ANESTHESIOLOGY DEVICES Monitoring Devices § 868.2385 Nitrogen dioxide analyzer. (a) Identification. The nitrogen dioxide analyzer is a device intended to measure the concentration of...

  16. 21 CFR 868.2385 - Nitrogen dioxide analyzer.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 8 2012-04-01 2012-04-01 false Nitrogen dioxide analyzer. 868.2385 Section 868...) MEDICAL DEVICES ANESTHESIOLOGY DEVICES Monitoring Devices § 868.2385 Nitrogen dioxide analyzer. (a) Identification. The nitrogen dioxide analyzer is a device intended to measure the concentration of...

  17. 40 CFR 52.728 Control strategy: Nitrogen dioxide. - [Reserved

    Code of Federal Regulations, 2014 CFR

    1998-07-01

    ... 40 Protection of Environment 3 1998-07-01 1998-07-01 false 52.728 Control strategy: Nitrogen dioxide. Section 52.728 Control strategy: Nitrogen dioxide. AIR PROGRAMS-(CONTINUED) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Illinois § 52.728Control strategy: Nitrogen dioxide....

  18. 21 CFR § 868.2385 - Nitrogen dioxide analyzer.

    Code of Federal Regulations, 2011 CFR

    2015-04-01

    ... 21 Food and Drugs 8 2015-04-01 2015-04-01 false Nitrogen dioxide analyzer. § 868.2385 Section Â... (CONTINUED) MEDICAL DEVICES ANESTHESIOLOGY DEVICES Monitoring Devices § 868.2385 Nitrogen dioxide analyzer. (a) Identification. The nitrogen dioxide analyzer is a device intended to measure the...

  19. 40 CFR 52.728 Control strategy: Nitrogen dioxide. - [Reserved

    Code of Federal Regulations, 2010 CFR

    1997-07-01

    ... 40 Protection of Environment 3 1997-07-01 1997-07-01 false 52.728 Control strategy: Nitrogen dioxide. Section 52.728 Control strategy: Nitrogen dioxide. AIR PROGRAMS-(CONTINUED) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Illinois § 52.728Control strategy: Nitrogen dioxide....

  20. 40 CFR 52.728 Control strategy: Nitrogen dioxide. - [Reserved

    Code of Federal Regulations, 2013 CFR

    1996-07-01

    ... 40 Protection of Environment 2 1996-07-01 1996-07-01 false 52.728 Control strategy: Nitrogen dioxide. Section 52.728 Control strategy: Nitrogen dioxide. AIR PROGRAMS (CONTINUED) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Illinois § 52.728Control strategy: Nitrogen dioxide....

  1. Analysis of Nitrogen Dioxide and Sulphur Dioxide in Lima, Peru: Trends and Seasonal Variations

    NASA Astrophysics Data System (ADS)

    Pacsi, S.; Rappenglueck, B.

    2007-12-01

    This research was carried out to show a general analysis of the monthly and yearly variation (1996-2002) and the tendency of the nitrogen dioxide (NO2) and sulfur dioxide (SO2) for the 5 stations of the air quality network of Lima. The SO2 and NO2 concentrations were measured by the Dirección General de Salud Ambiental (DIGESA), using the active sampling method and the chemical analysis has been determined by Turbidimetry and Colorimetry for the SO2 and NO2 respectively. The monthly average variation (1996-2001) of SO2 in the Lima Center station has a small annual range (32,4 mikrograms/m3) with maximum values in autumn (April) and minimum in winter (June). The NO2 presents a higher annual range (128,2 mikrograms/m3) and its minimum values occur in the summer and the maximum in spring. The annual averages analysis (2000-2002) of the air quality monitoring network of Lima shows that the SO2 and NO2 values are maximum in the Lima Center station and exceed the Peruvian air quality standard (ECAs) in 30% and 75% respectively. The yearly variation (1996-2001) in the Lima Center station show an increasing tendency in the SO2 (significant) and NO2 (not significant) values, which indicates the critical level of the air quality in Lima, therefore the implementation of the air pollution control programs is urgent.

  2. 40 CFR Appendix F to Part 50 - Measurement Principle and Calibration Procedure for the Measurement of Nitrogen Dioxide in the...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... Procedure for the Measurement of Nitrogen Dioxide in the Atmosphere (Gas Phase Chemiluminescence) F Appendix...—Measurement Principle and Calibration Procedure for the Measurement of Nitrogen Dioxide in the Atmosphere (Gas... concentration standard. NO2 concentration standard. 2.1 Principle. Atmospheres containing accurately...

  3. 40 CFR Appendix F to Part 50 - Measurement Principle and Calibration Procedure for the Measurement of Nitrogen Dioxide in the...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Procedure for the Measurement of Nitrogen Dioxide in the Atmosphere (Gas Phase Chemiluminescence) F Appendix...—Measurement Principle and Calibration Procedure for the Measurement of Nitrogen Dioxide in the Atmosphere (Gas... concentration standard. NO2 concentration standard. 2.1 Principle. Atmospheres containing accurately...

  4. 40 CFR Appendix F to Part 50 - Measurement Principle and Calibration Procedure for the Measurement of Nitrogen Dioxide in the...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Procedure for the Measurement of Nitrogen Dioxide in the Atmosphere (Gas Phase Chemiluminescence) F Appendix...—Measurement Principle and Calibration Procedure for the Measurement of Nitrogen Dioxide in the Atmosphere (Gas... concentration standard. NO2 concentration standard. 2.1 Principle. Atmospheres containing accurately...

  5. Home interventions are effective at decreasing indoor nitrogen dioxide concentrations

    PubMed Central

    Paulin, L. M.; Diette, G. B.; Scott, M.; McCormack, M. C.; Matsui, E. C.; Curtin-Brosnan, J.; Williams, D. L.; Kidd-Taylor, A.; Shea, M.; Breysse, P. N.; Hansel, N. N.

    2016-01-01

    Nitrogen dioxide (NO2), a by-product of combustion produced by indoor gas appliances such as cooking stoves, is associated with respiratory symptoms in those with obstructive airways disease. We conducted a three-armed randomized trial to evaluate the efficacy of interventions aimed at reducing indoor NO2 concentrations in homes with unvented gas stoves: (i) replacement of existing gas stove with electric stove; (ii) installation of ventilation hood over existing gas stove; and (iii) placement of air purifiers with high-efficiency particulate air (HEPA) and carbon filters. Home inspection and NO2 monitoring were conducted at 1 week pre-intervention and at 1 week and 3 months post-intervention. Stove replacement resulted in a 51% and 42% decrease in median NO2 concentration at 3 months of follow-up in the kitchen and bedroom, respectively (P = 0.01, P = 0.01); air purifier placement resulted in an immediate decrease in median NO2 concentration in the kitchen (27%, P < 0.01) and bedroom (22%, P = 0.02), but at 3 months, a significant reduction was seen only in the kitchen (20%, P = 0.05). NO2 concentrations in the kitchen and bedroom did not significantly change following ventilation hood installation. Replacing unvented gas stoves with electric stoves or placement of air purifiers with HEPA and carbon filters can decrease indoor NO2 concentrations in urban homes. PMID:24329966

  6. Simultaneous sulfur dioxide and nitrogen dioxide removal by calcium hydroxide and calcium silicate solids.

    PubMed

    Nelli, C H; Rochelle, G T

    1998-09-01

    At conditions typical of a bag filter exposed to a coal-fired flue gas that has been adiabatically cooled with water, calcium hydroxide and calcium silicate solids were exposed to a dilute, humidified gas stream of nitrogen dioxide (NO2) and sulfur dioxide (SO2) in a packed-bed reactor. A prior study found that NO2 reacted readily with surface water of alkaline and non-alkaline solids to produce nitrate, nitrite, and nitric oxide (NO). With SO2 present in the gas stream, NO2 also reacted with S(IV), a product of SO2 removal, on the exterior of an alkaline solid. The oxidation of S(IV) to S(VI) by oxygen reduced the availability of S(IV) and lowered removal of NO2. Subsequent acidification of the sorbent by the removal of NO2 and SO2 facilitated the production of NO. However, the conversion of nitrous acid to sulfur-nitrogen compounds reduced NO production and enhanced SO2 removal. A reactor model based on empirical and semi-empirical rate expressions predicted rates of SO2 removal, NO2 removal, and NO production by calcium silicate solids. Rate expressions from the reactor model were inserted into a second program, which predicted the removal of SO2 and NOx by a continuous process, such as the collection of alkaline solids in a baghouse. The continuous process model, depending upon inlet conditions, predicted 30-40% removal for NOx and 50-90% removal for SO2. These results are relevant to dry scrubbing technology for combined SO2 and NOx removal that first oxidizes NO to NO2 by the addition of methanol into the flue duct. PMID:9775761

  7. Evaluation of land use regression models (LURs) for nitrogen dioxide and benzene in four U.S. Cities.

    EPA Science Inventory

    Spatial analysis studies have included application of land use regression models (LURs) for health and air quality assessments. Recent LUR studies have collected nitrogen dioxide (NO2) and volatile organic compounds (VOCs) using passive samplers at urban air monitoring networks ...

  8. Comparison of Satellite Observations of Nitrogen Dioxide to Surface Monitor Nitrogen Dioxide Concentration

    NASA Technical Reports Server (NTRS)

    Kleb, Mary M.; Pippin, Margaret R.; Pierce, R. Bradley; Neil, Doreen O.; Lingenfelser, Gretchen; Szykman, James J.

    2006-01-01

    Nitrogen dioxide is one of the U. S. EPA s criteria pollutants, and one of the main ingredients needed for the production of ground-level ozone. Both ozone and nitrogen dioxide cause severe public health problems. Existing satellites have begun to produce observational data sets for nitrogen dioxide. Under NASAs Earth Science Applications Program, we examined the relationship between satellite observations and surface monitor observations of this air pollutant to examine if the satellite data can be used to facilitate a more capable and integrated observing network. This report provides a comparison of satellite tropospheric column nitrogen dioxide to surface monitor nitrogen dioxide concentration for the period from September 1996 through August 1997 at more than 300 individual locations in the continental US. We found that the spatial resolution and observation time of the satellite did not capture the variability of this pollutant as measured at ground level. The tools and processes developed to conduct this study will be applied to the analysis of advanced satellite observations. One advanced instrument has significantly better spatial resolution than the measurements studied here and operates with an afternoon overpass time, providing a more representative distribution for once-per-day sampling of this photochemically active atmospheric constituent.

  9. Hemispherical Scanning Imaging DOAS: Resolving nitrogen dioxide in the urban environment

    NASA Astrophysics Data System (ADS)

    Leigh, R. J.; Graves, R. R.; Lawrence, J.; Faloon, K.; Monks, P. S.

    2012-12-01

    Imaging DOAS techniques have been used for nitrogen dioxide and sulfer dioxide for a number of years. This presentation describes a novel system which images concentrations of nitrogen dioxide by scanning an imaging spectrometer 360 degrees azimuthally, covering a region from 5 degrees below the horizon, to the zenith. The instrument has been built at the University of Leicester (UK), on optical designs by Surrey Satellite Technologies Ltd, and incorporates an Offner relay with Schwarzchild fore-optics, in a rotating mount. The spectrometer offers high fidelity spectroscopic retrievals of nitrogen dioxide as a result of a reliable Gaussian line shape, zero smile and low chromatic aberration. The full hemispherical scanning provides complete coverage of nitrogen dioxide concentrations above approximately 5 ppbv in urban environments. Through the use of multiple instruments, the three-dimensional structure of nitrogen dioxide can be sampled and tomographically reconstructed, providing valuable information on nitrogen dioxide emissions and downwind exposure, in addition to new understanding of boundary layer dynamics through the use of nitrogen dioxide as a tracer. Furthermore, certain aerosol information can be retrieved through absolute intensity measurements in each azimuthal direction supplemented by traditional techniques of O4 spectroscopy. Such measurements provide a new tool for boundary layer measurement and monitoring at a time when air quality implications on human health and climate are under significant scrutiny. This presentation will describe the instrument and tomographic potential of this technique. First measurements were taken as part of the international PEGASOS campaign in Bologna, Italy. Results from these measurements will be shown, including imaging of enhanced NO2 in the Bologna urban boundary layer during a severe thunderstorm. A Hemispherical Scanning Imaging DOAS instrument operating in Bologna, Italy in June 2012. Visible in the background

  10. Household levels of nitrogen dioxide and pediatric asthma severity

    PubMed Central

    Belanger, Kathleen; Holford, Theodore R.; Gent, Janneane F.; Hill, Melissa E.; Kezik, Julie M.; Leaderer, Brian P.

    2013-01-01

    Background Adverse respiratory effects in children with asthma are associated with exposures to nitrogen dioxide (NO2). Levels indoors can be much higher than outdoors. Primary indoor sources of NO2 are gas stoves, which are used for cooking by one-third of US households. We investigated effects of indoor NO2 exposure on asthma severity among an ethnically and economically diverse sample of children, controlling for season and indoor allergen exposure. Methods Children aged 5–10 years with active asthma (n=1,342), were recruited through schools in urban and suburban Connecticut and Massachusetts (2006–2009) for a prospective, year-long study with seasonal measurements of NO2 and asthma severity. Exposure to NO2 was measured passively for four, month-long, periods with Palmes tubes. Asthma morbidity was concurrently measured by a severity score and frequency of wheeze, night symptoms and use of rescue medication. We used adjusted, hierarchical ordered logistic regression models to examine associations between household NO2 exposure and health outcomes. Results Every 5 ppb increase in NO2 exposure above a threshold of 6 ppb was associated with a dose-dependent increase in risk of higher asthma severity score (odds ratio= 1.37 [95% confidence interval= 1.01 – 1.89]), wheeze (1.49 [1.09 – 2.03]), night symptoms (1.52 [1.16 – 2.00]) and rescue medication use (1.78 [1.33 – 2.38]). Conclusions Asthmatic children exposed to NO2 indoors, at levels well below the US Environmental Protection Agency outdoor standard (53 ppb), are at risk for increased asthma morbidity. Risks are not confined to inner-city children, but occur at NO2 concentrations common in urban and suburban homes. PMID:23337243

  11. 40 CFR 52.1876 - Control strategy: Nitrogen dioxide.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...: Nitrogen dioxide. (a) The condition to EPA's approval of the oxides of nitrogen State Implementation Plan (SIP) codified at 40 CFR 52.1870(c)(128) is satisfied by Ohio's November 26, 2003, submittal of the... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Nitrogen dioxide....

  12. 40 CFR 52.1576 - Control strategy: Nitrogen dioxide.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Nitrogen dioxide. 52... strategy: Nitrogen dioxide. (a) The requirements of § 52.14(c)(3) of this chapter as of May 8, 1974 (39 FR 16346), are not met since the plan does not provide for the degree of nitrogen oxides emission...

  13. 40 CFR 52.1876 - Control strategy: Nitrogen dioxide.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...: Nitrogen dioxide. (a) The condition to EPA's approval of the oxides of nitrogen State Implementation Plan (SIP) codified at 40 CFR 52.1870(c)(128) is satisfied by Ohio's November 26, 2003, submittal of the... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Control strategy: Nitrogen dioxide....

  14. 40 CFR 52.1876 - Control strategy: Nitrogen dioxide.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...: Nitrogen dioxide. (a) The condition to EPA's approval of the oxides of nitrogen State Implementation Plan (SIP) codified at 40 CFR 52.1870(c)(128) is satisfied by Ohio's November 26, 2003, submittal of the... 40 Protection of Environment 4 2014-07-01 2014-07-01 false Control strategy: Nitrogen dioxide....

  15. 40 CFR 52.1876 - Control strategy: Nitrogen dioxide.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...: Nitrogen dioxide. (a) The condition to EPA's approval of the oxides of nitrogen State Implementation Plan (SIP) codified at 40 CFR 52.1870(c)(128) is satisfied by Ohio's November 26, 2003, submittal of the... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Nitrogen dioxide....

  16. 40 CFR 52.1876 - Control strategy: Nitrogen dioxide.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...: Nitrogen dioxide. (a) The condition to EPA's approval of the oxides of nitrogen State Implementation Plan (SIP) codified at 40 CFR 52.1870(c)(128) is satisfied by Ohio's November 26, 2003, submittal of the... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Nitrogen dioxide....

  17. A Continuous Flow System for the Measurement of Ambient Nitrogen Oxides [NO + NO2] Using Rhodamine B Hydrazide as a Chemosensor.

    PubMed

    Malingappa, Pandurangappa; Yarradoddappa, Venkataramanappa

    2014-01-01

    A new chemosensor has been used to monitor atmospheric nitrogen oxides [NO + NO2] at parts per billion (ppb) level. It is based on the catalytic reaction of nitrogen oxides with rhodamine B hydrazide (RBH) to produce a colored compound through the hydrolysis of the amide bond of the molecule. A simple colorimeter has been used to monitor atmospheric nitrogen dioxide at ppb level. The air samples were purged through a sampling cuvette containing RBH solution using peristaltic pump. The proposed method has been successfully applied to monitor the ambient nitrogen dioxide levels at traffic junction points within the city limits and the results obtained are compared with the standard Griess-Ilosvay method. PMID:25210422

  18. A Continuous Flow System for the Measurement of Ambient Nitrogen Oxides [NO + NO2] Using Rhodamine B Hydrazide as a Chemosensor

    PubMed Central

    Malingappa, Pandurangappa; Yarradoddappa, Venkataramanappa

    2014-01-01

    A new chemosensor has been used to monitor atmospheric nitrogen oxides [NO + NO2] at parts per billion (ppb) level. It is based on the catalytic reaction of nitrogen oxides with rhodamine B hydrazide (RBH) to produce a colored compound through the hydrolysis of the amide bond of the molecule. A simple colorimeter has been used to monitor atmospheric nitrogen dioxide at ppb level. The air samples were purged through a sampling cuvette containing RBH solution using peristaltic pump. The proposed method has been successfully applied to monitor the ambient nitrogen dioxide levels at traffic junction points within the city limits and the results obtained are compared with the standard Griess-Ilosvay method. PMID:25210422

  19. Total nitrogen dioxide at the Arctic polar circle since 1990

    SciTech Connect

    Goutail, F.; Pommereau, J.P.; Sarkissian, A. ); Kyro, E. ); Dorokhov, V.

    1994-06-22

    This article presents results of nitrogen dioxide measurements from a station in northern Finland (67.3[degrees]N) since January 1990, and stations in Greenland, northern Atlantic, and eastern Siberia, during EASOE. The nitrogen dioxide levels are seen to have fallen at least 30 % since the arrival of the volcanic aerosols from the Mt. Pinatubo eruption. The winter results are not supportive of strong denitrification, or of the expected level of vapor nitrogen dioxide during winter months.

  20. Nitrogen dioxide, sulfur dioxide, and ammonia detector for remote sensing of vehicle emissions

    NASA Astrophysics Data System (ADS)

    Burgard, Daniel A.; Dalton, Thomas R.; Bishop, Gary A.; Starkey, John R.; Stedman, Donald H.

    2006-01-01

    A remote sensor for measuring on-road vehicles passing the sensor in real time is described. This sensor expands upon previous technology that measured carbon monoxide, carbon dioxide, and exhaust hydrocarbons in the IR and nitric oxide in the UV. The design adds the capability to measure nitrogen dioxide in the UV with one spectrometer and to measure SO2 and NH3 along with NO in a second UV spectrometer. With these units operating side by side, the major mobile source precursors to secondary aerosol production can be measured simultaneously and in real time. Detection limits for NO2, SO2, and NH3 are 1.2, 0.72, and 0.78 g pollutant per kilogram of fuel, respectively.

  1. Study of solar variability impact on nitrogen dioxide: 2004-2013

    NASA Astrophysics Data System (ADS)

    Constantin, Daniel-Eduard; Voiculescu, Mirela; Merlaud, Alexis; Van Roozendael, Michel

    2015-04-01

    Nitrogen dioxide (NO2) locally plays an important role in the radiation budget by absorbing solar radiation at ultraviolet (UV) and visible wavelengths. The influence of solar variability on the inter-annual variability and trends in nitrogen dioxide is evaluated for a period of 10 years (2004-2013) using monthly mean tropospheric NO2 measurements of the Ozone Monitoring Instrument (OMI) version 2.0. Possible signatures of solar variability on nitrogen dioxide time series of NO2 over several cities were analyzed using various statistical methods. Various solar proxies were selected, in order to separate between possible links to solar irradiance and to solar wind. Several locations with different levels of pollution, located in different places of the world (Athens, Jungfraujoch, Lauder, Lisbon, Moscow, and Uccle), were selected. Observations show a clear 27 day period of the NO2 tropospheric Vertical Column Density (VCD) or total Slant Column Density (SCD). NO2 content decreases with increasing activity above polluted areas (e.g. Athens, Moscow) while for unpolluted areas there is no evident correlation (e.g. Lauder, Jungfraujoch). Possible effects of solar wind on NO2 content are observed as well, but the relationship is less clear, since polluted areas seem to respond differently to solar wind variations. The mechanism by which NO2 content can be affected by solar variations relate mainly to ozone production but other paths by which solar energy may be transferred to the lower atmosphere are investigated.

  2. An Improved Retrieval of Tropospheric Nitrogen Dioxide from GOME

    NASA Technical Reports Server (NTRS)

    Martin, Randall V.; Chance, Kelly; Jacob, Daniel J.; Kurosu, Thomas P.; Spurr, Robert J. D.; Bucsela, Eric; Gleason, James F.; Palmer, Paul I.; Bey, Isabelle; Fiore, Arlene M.

    2002-01-01

    We present a retrieval of tropospheric nitrogen dioxide (NO2) columns from the Global Ozone Monitoring Experiment (GOME) satellite instrument that improves in several ways over previous retrievals, especially in the accounting of Rayleigh and cloud scattering. Slant columns, which are directly fitted without low-pass filtering or spectral smoothing, are corrected for an artificial offset likely induced by spectral structure on the diffuser plate of the GOME instrument. The stratospheric column is determined from NO2 columns over the remote Pacific Ocean to minimize contamination from tropospheric NO2. The air mass factor (AMF) used to convert slant columns to vertical columns is calculated from the integral of the relative vertical NO2 distribution from a global 3-D model of tropospheric chemistry driven by assimilated meteorological data (Global Earth Observing System (GEOS)-CHEM), weighted by altitude dependent scattering weights computed with a radiative transfer model (Linearized Discrete Ordinate Radiative Transfer), using local surface albedos determined from GOME observations at NO2 wavelengths. The AMF calculation accounts for cloud scattering using cloud fraction, cloud top pressure, and cloud optical thickness from a cloud retrieval algorithm (GOME Cloud Retrieval Algorithm). Over continental regions with high surface emissions, clouds decrease the AMT by 20- 30% relative to clear sky. GOME is almost twice as sensitive to tropospheric NO2 columns over ocean than over land. Comparison of the retrieved tropospheric NO2 columns for July 1996 with GEOS-CHEM values tests both the retrieval and the nitrogen oxide radical (NOx) emissions inventories used in GEOS-CHEM. Retrieved tropospheric NO2 columns over the United States, where NOx emissions are particularly well known, are within 18% of GEOS-CHEM columns and are strongly spatially correlated (r = 0.78, n = 288, p less than 0.005). Retrieved columns show more NO2 than GEOS-CHEM columns over the Transvaal

  3. Low-energy positron and electron scattering from nitrogen dioxide

    NASA Astrophysics Data System (ADS)

    Chiari, Luca; Zecca, Antonio; García, Gustavo; Blanco, Francisco; Brunger, M. J.

    2013-12-01

    Total cross section (TCS) measurements for positron scattering from nitrogen dioxide (NO2) are presented in the energy range 0.2-40 eV. The TCS, the elastic integral and differential cross sections, and the integral cross section accounting of all the inelastic processes (including positronium formation) have also been computed using the independent atom model with screening corrected additivity rule (IAM-SCAR) for incident energies from 1 to 1000 eV. A qualitative level of agreement is found between the present TCS experiment and theory at the common energies. As no previous measurements or calculations for positron-NO2 scattering exist in the literature, we also computed the TCS for electron collisions with NO2 employing the IAM-SCAR method. A comparison of those results to the present positron cross sections and the earlier electron-impact data and calculations is provided. To investigate the role that chemical substitution plays in positron scattering phenomena, we also compare the present positron-NO2 data with the TCSs measured at the University of Trento for positron scattering from N2O and CO2.

  4. Remote sensing of ammonia, sulfur dioxide, and nitrogen dioxide emissions from cars and trucks

    NASA Astrophysics Data System (ADS)

    Burgard, Daniel Alexander

    This document describes the development of a remote sensor for mobile source ammonia (NH3), sulfur dioxide (SO2), and nitrogen dioxide (NO2) based on an instrument previously developed at the University of Denver. Significant optical upgrades allow for the detection of three new species. Detection and quantification of NH3 and SO 2 use wavelengths deeper into the ultraviolet region than previously possible. Currently NH3 is quantified from three peaks at 209 nm, 213 nm, and 217 nm; SO2 from three peaks at 219 nm, 221 nm, and 222 nm; NO2 using the spectral window 430--446 nm. The instrument was demonstrated in the measurement of emissions from both gasoline and diesel light duty vehicles and heavy duty diesel trucks (HDDT). The remote sensor was used for over 20,000 measurements of NH3 and SO2 emissions from motor vehicles in Denver and Tulsa in the summer of 2005. Nitrogen dioxide emissions were measured at the Denver site only. For the first time, on-road vehicle NH3 and SO2 emission trends versus model year were observed. Ammonia is a larger percentage of the exhaust than previously predicted for newer vehicles and its production reaches a maximum with approximately the 1996 model year. NH3 is the first pollutant observed to have lower emissions from the oldest model year. Sulfur dioxide emissions decrease with newer model year vehicles. Nearly 1200 NH3, SO2, and NO2 emission measurements with valid vehicle identification numbers were collected from in-use HDDTs in Golden and Dumont, CO. The Dumont weigh station site allowed emissions to be correlated with gross vehicle weight. No trends were apparent. The Golden site allowed emissions to be correlated with odometer and a trend of increasing oxides of nitrogen (NOx) emissions was apparent even near one million miles, when some vehicles should show lower emissions due to engine rebuild and computer reflash. For the first time HDDT on-road NO x emissions were shown versus vehicle model year and found to reach a

  5. 40 CFR 52.1676 - Control strategy: Nitrogen dioxide.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... August 10, 1979, is disapproved because it is inconsistent with 40 CFR Subpart G, Control strategy... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Control strategy: Nitrogen dioxide. 52...: Nitrogen dioxide. (a) The requirements of § 52.14(c)(3) of this chapter as of May 8, 1974 (39 FR...

  6. 40 CFR 52.1676 - Control strategy: Nitrogen dioxide.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... August 10, 1979, is disapproved because it is inconsistent with 40 CFR Subpart G, Control strategy... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Nitrogen dioxide. 52...: Nitrogen dioxide. (a) The requirements of § 52.14(c)(3) of this chapter as of May 8, 1974 (39 FR...

  7. 40 CFR 52.1676 - Control strategy: Nitrogen dioxide.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... August 10, 1979, is disapproved because it is inconsistent with 40 CFR Subpart G, Control strategy... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Nitrogen dioxide. 52...: Nitrogen dioxide. (a) The requirements of § 52.14(c)(3) of this chapter as of May 8, 1974 (39 FR...

  8. 40 CFR 52.1676 - Control strategy: Nitrogen dioxide.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... August 10, 1979, is disapproved because it is inconsistent with 40 CFR Subpart G, Control strategy... 40 Protection of Environment 4 2014-07-01 2014-07-01 false Control strategy: Nitrogen dioxide. 52...: Nitrogen dioxide. (a) The requirements of § 52.14(c)(3) of this chapter as of May 8, 1974 (39 FR...

  9. 40 CFR 52.1676 - Control strategy: Nitrogen dioxide.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... August 10, 1979, is disapproved because it is inconsistent with 40 CFR Subpart G, Control strategy... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Nitrogen dioxide. 52...: Nitrogen dioxide. (a) The requirements of § 52.14(c)(3) of this chapter as of May 8, 1974 (39 FR...

  10. Purification of crude hexafluoroacetone containing nitrogen oxides and sulfur dioxide

    SciTech Connect

    Bonfield, J. H.; Karsay, B. I.

    1984-09-25

    Crude hexafluoroacetone containing as impurities nitrogen oxides and sulfur dioxide is purified by admixing with water to form an aqueous solution, admixing the aqueous solution with concentrated sulfuric acid or oleum to form a vapor and scrubbing the vapor with liquid concentrated sulfuric acid to produce purified anhydrous hexafluoroacetone. The sulfur dioxide and nitrogen oxides interact with the aqueous solution and conc

  11. Current nitrogen dioxide exposures among railroad workers

    SciTech Connect

    Woskie, S.R.; Hammond, S.K.; Smith, T.J.; Schenker, M.B. )

    1989-07-01

    As part of a series of epidemiologic studies of the mortality patterns of railroad workers, various air contaminants were measured to characterize the workers' current exposures to diesel exhaust. Nitrogen dioxide (NO{sub 2}), which is a constituent of diesel exhaust, was examined as one possible marker of diesel exposure. An adaptation of the Palmes personal passive sampler was used to measure the NO{sub 2} exposures of 477 U.S. railroad workers at four railroads. The range of NO{sub 2} exposures expressed as the arithmetic average +/- two standard errors for the five career job groups were as follows: signal maintainers, 16-24 parts per billion (ppb); clerks/dispatchers/station agents, 23-43 ppb; engineers/firers, 26-38 ppb; brakers/conductors, 50-74 ppb; and locomotive shop workers, 95-127 ppb. Variations among railroads and across seasons were not significant for most job groups.

  12. Pretreatment with nitrogen dioxide modifies plant response to ozone

    NASA Astrophysics Data System (ADS)

    Runeckles, V. C.; Palmer, K.

    Plant growth inhibition by ozone is significantly affected by previous exposure to nitrogen dioxide. Experiments on the early growth of four crop species showed that daily pretreatment with NO 2 (0.08-0.10 ppm for 3 h) immediately prior to exposure to O 3 (0.08-0.10 ppm for 6 h) increased the inhibition of radish and wheat growth, decreased the inhibition of bush bean growth, but had no effect on the growth of mint. The magnitudes of the interactive effects indicate that in regions where relatively high concentrations of O 3 are produced by photochemical processes, for example, downwind from urban centres, assessments of the impact of O 3 on vegetation based on knowledge of response to O 3 alone may be seriously flawed.

  13. NEAR-LIFETIME EXPOSURE OF THE RAT TO A SIMULATED URBAN PROFILE OF NITROGEN DIOXIDE: PULMONARY FUNCTION EVALUATION

    EPA Science Inventory

    To investigate the potential for near-ambient levels of nitrogen dioxide (NO2) to induce functional lung damage, groups of rats were exposed to air or a simulated urban profile of NO2 (0.5 ppm, 1.5 ppm peak) for 1, 3, 13, 52, or 78 weeks. The dynamic, static, and diffusional char...

  14. CHARACTERIZATION OF A SPATIAL GRADIENT OF NITROGEN DIOXIDE ACROSS A UNITED STATES-MEXICO BORDER CITY DURING WINTER

    EPA Science Inventory

    A gradient of ambient nitrogen dioxide (NO2) concentration is demonstrated across metropolitan El Paso, Texas (USA), a city located on the international border between the United States and Mexico. Integrated measurements of NO2 were collected over seven days at 20 elementary sc...

  15. Liquid crystal-based sensors for selective and quantitative detection of nitrogen dioxide.

    PubMed

    Sen, Avijit; Kupcho, Kurt A; Grinwald, Bart A; Vantreeck, Heidi J; Acharya, Bharat R

    2013-03-01

    A highly sensitive nitrogen dioxide (NO2) sensor based on orientational transition of a thin film of liquid crystal (LC) supported on a gold surface is reported. Transport of NO2 molecules through the LC film to the LC-gold interface induces an orientation transition in the LC film. The dynamic behavior of the sensor response exhibits a concentration-dependent response rate that is employed to generate an algorithm for quantitative determination of unknown concentrations. Sensitive, selective and reversible detection with minimal effects of environmental fluctuations suggest that these sensors can be used for quantitative NO2 detection for a number of applications. PMID:23526230

  16. Novel nighttime free radical chemistry in severe nitrogen dioxide pollution episodes

    NASA Astrophysics Data System (ADS)

    Harrison, Roy M.; Shi, Ji Ping; Grenfell, J. Lee.

    During winter air pollution episodes, nitrogen dioxide concentrations can far exceed health based guidelines, but to date, there has been no wholly adequate explanation of the atmospheric chemical production of very high concentrations of nitrogen dioxide during such episodes, despite inclusion of the thermal oxidation of nitric oxide with dioxygen, as well as the well known reaction with ozone. In laboratory studies we have shown that both petrol engine exhaust and petrol vapour catalyse the thermal oxidation of nitric oxide to nitrogen dioxide and have identified certain dialkenes as the chemical agent responsible ( Shi and Harrison, 1997). It is postulated that addition of nitrogen dioxide to the dialkene forms a reactive free radical species which initiates a chain reaction during which peroxy species are formed which convert NO to NO 2. A numerical box model including explicit hydrocarbon chemistry and incorporating this mechanism, shows that rates of nitrogen dioxide production observed in London in December 1991 and hitherto unexplained, are explicable by the presence of conjugate dialkenes at concentrations comparable with those which have been observed in polluted urban atmospheres.

  17. Inventory of nitrogen oxide emissions derived from space-based observations of NO2 columns

    NASA Astrophysics Data System (ADS)

    Martin, R. V.; Jacob, D. J.; Chance, K. V.; Kurosu, T. P.; Palmer, P. I.; Evans, M. J.

    2003-04-01

    Nitrogen oxide radicals (NO_x = NO + NO_2) largely control tropospheric ozone production. We construct a global inventory of nitrogen oxide emissions using top-down information from our retrieval of tropospheric NO_2 columns (1996--97) from the European Space Agency's Global Ozone Monitoring Experiment (GOME) satellite instrument. We combine the top-down information with an a priori bottom-up inventory (based on the Global Emission Inventory Activity (GEIA) and scaled to 1996--97) weighted by relative errors in the top-down and bottom-up sources. We calculate the local relationship between NO_2 columns and NO_x emissions with a global 3-D model of tropospheric chemistry (GEOS-CHEM) that uses the a priori inventory. Monthly mean top-down errors in NO_x emissions of 50% at 2^ox2.5^o resolution are comparable to bottom-up errors over industrial regions and much better elsewhere. A posteriori errors are about half of a priori errors. Global annual land surface NO_x emissions for the a priori, an independent inventory (EDGAR 3.0), and the a posteriori are 36.4, 36.6, and 37.7 Tg N yr-1 respectively. Local a posteriori NO_x emissions suggest underestimates of up to a factor of 2 near Johannesburg, Tehran, and Riyadh, up to 50% for Spain, Tokyo, and the Po Valley of Italy, and 25% for the eastern United States, as well as local overestimates of up to 50% for India and the biomass burning regions of central Africa and Brazil. A posteriori NO_x emissions provide evidence that soil NO_x emissions are underestimated for the western United States, Spain, the Sahel, and the Mediterranean coastal region.

  18. PHOTOCHEMICAL REACTIONS AMONG FORMALDEHYDE, CHLORINE, AND NITROGEN DIOXIDE IN AIR

    EPA Science Inventory

    Photochemical reactions among chlorine, nitrogen dioxide, and formaldehyde were studied, using parts-per-million concentrations in 1 atm of air. The reactant mixtures were irradiated by ultraviolet fluorescent lamps and simultaneously analyzed by the Fourier transform infrared te...

  19. 49 CFR 173.336 - Nitrogen dioxide, liquefied, or dinitrogen tetroxide, liquefied.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 49 Transportation 2 2014-10-01 2014-10-01 false Nitrogen dioxide, liquefied, or dinitrogen....336 Nitrogen dioxide, liquefied, or dinitrogen tetroxide, liquefied. (a) Nitrogen dioxide, liquefied... with nitrogen dioxide. Each valve opening must be closed by a solid metal plug with tapered...

  20. 49 CFR 173.336 - Nitrogen dioxide, liquefied, or dinitrogen tetroxide, liquefied.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 49 Transportation 2 2011-10-01 2011-10-01 false Nitrogen dioxide, liquefied, or dinitrogen....336 Nitrogen dioxide, liquefied, or dinitrogen tetroxide, liquefied. (a) Nitrogen dioxide, liquefied... with nitrogen dioxide. Each valve opening must be closed by a solid metal plug with tapered...

  1. 49 CFR 173.336 - Nitrogen dioxide, liquefied, or dinitrogen tetroxide, liquefied.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 49 Transportation 2 2010-10-01 2010-10-01 false Nitrogen dioxide, liquefied, or dinitrogen....336 Nitrogen dioxide, liquefied, or dinitrogen tetroxide, liquefied. (a) Nitrogen dioxide, liquefied... with nitrogen dioxide. Each valve opening must be closed by a solid metal plug with tapered...

  2. 49 CFR 173.336 - Nitrogen dioxide, liquefied, or dinitrogen tetroxide, liquefied.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 49 Transportation 2 2012-10-01 2012-10-01 false Nitrogen dioxide, liquefied, or dinitrogen....336 Nitrogen dioxide, liquefied, or dinitrogen tetroxide, liquefied. (a) Nitrogen dioxide, liquefied... with nitrogen dioxide. Each valve opening must be closed by a solid metal plug with tapered...

  3. Global inventory of nitrogen oxide emissions constrained by space-based observations of NO2 columns

    NASA Astrophysics Data System (ADS)

    Martin, Randall V.; Jacob, Daniel J.; Chance, Kelly; Kurosu, Thomas P.; Palmer, Paul I.; Evans, Mathew J.

    2003-09-01

    We use tropospheric NO2 columns from the Global Ozone Monitoring Experiment (GOME) satellite instrument to derive top-down constraints on emissions of nitrogen oxides (NOx ≡ NO + NO2), and combine these with a priori information from a bottom-up emission inventory (with error weighting) to achieve an optimized a posteriori estimate of the global distribution of surface NOx emissions. Our GOME NO2 retrieval improves on previous work by accounting for scattering and absorption of radiation by aerosols; the effect on the air mass factor (AMF) ranges from +10 to -40% depending on the region. Our AMF also includes local information on relative vertical profiles (shape factors) of NO2 from a global 3-D chemical transport model (GEOS-CHEM); assumption of a globally uniform shape factor, as in most previous retrievals, would introduce regional biases of up to 40% over industrial regions and a factor of 2 over remote regions. We derive a top-down NOx emission inventory from the GOME data by using the local GEOS-CHEM relationship between NO2 columns and NOx emissions. The resulting NOx emissions for industrial regions are aseasonal, despite large seasonal variation in NO2 columns, providing confidence in the method. Top-down errors in monthly NOx emissions are comparable with bottom-up errors over source regions. Annual global a posteriori errors are half of a priori errors. Our global a posteriori estimate for annual land surface NOx emissions (37.7 Tg N yr-1) agrees closely with the GEIA-based a priori (36.4) and with the EDGAR 3.0 bottom-up inventory (36.6), but there are significant regional differences. A posteriori NOx emissions are higher by 50-100% in the Po Valley, Tehran, and Riyadh urban areas, and by 25-35% in Japan and South Africa. Biomass burning emissions from India, central Africa, and Brazil are lower by up to 50%; soil NOx emissions are appreciably higher in the western United States, the Sahel, and southern Europe.

  4. Nitrogen Dioxide Trend over the United States: the View from the Ground, the View from Space

    NASA Technical Reports Server (NTRS)

    Lamsal, Lok N.; Duncan, Bryan N.; Yoshida, Yasuko; Krotkov, Nickolay A.

    2014-01-01

    Emissions of nitrogen oxides (NOx) are decreasing over the US due to environmental policies and technological change. We use observations of tropospheric nitrogen dioxide (NO2) columns from the Ozone Monitoring Instrument (OMI) satellite instrument and surface NO2 in-situ measurements from the air quality system (AQS) to quantify the trends, and to establish the relationship between the trends in tropospheric column and surface concentration. Both observations show substantial downward trends from 2005 to 2013, with an average reduction of 35 percent according to OMI and 38 percent according to AQS. The annual reduction rates are largest in 2005-2009: -6.2 percent per year and -7 percent per year observed by OMI and AQS, respectively. We examine various factors affecting the estimated trend in OMI NO2 columns and in-situ NO2 observations. An improved understanding of trend offers valuable insights about effectiveness of emission reduction regulations on state and federal level.

  5. Nitrogen isotope exchange between NO and NO2 and its implications for δ15N variations in tropospheric NOx and atmospheric nitrate

    NASA Astrophysics Data System (ADS)

    Walters, Wendell W.; Simonini, Damian S.; Michalski, Greg

    2016-01-01

    The nitrogen (N) isotope exchange between nitric oxide (NO) and nitrogen dioxide (NO2) has been previously suggested to influence N stable isotope compositions (δ15N) of these molecules. However, there is disagreement in the magnitude of the N isotopic fractionation (αNO2>/NO) resulting from this exchange process between previous experimental and theoretical studies. To this end, we measured αNO2>/NO associated with this exchange reaction at various temperatures. Our results indicate αNO2>/NO to be 1.0403 ± 0.0015, 1.0356 ± 0.0015, and 1.0336 ± 0.0014 at 278 K, 297 K, and 310 K, respectively. These measured values are within experimental error of the values we calculated using a modified version of the Bigeleisen-Mayer equation corrected for accurate zero-point energies, indicating an agreement between experiment and theory. Modeling of this exchange reaction demonstrates that δ15N-NO2 may exhibit a diurnal and seasonal profile if N isotopic equilibrium is achieved.

  6. Monitoring of nitrogen dioxide, ozone and halogens radicals in Antarctica

    NASA Astrophysics Data System (ADS)

    Bortoli, Daniele; Ravegnani, Fabrizio; Costa, Maria J.; Genco, Silvia; Kulkarni, Pavan K.; Mendes, Rui; Domingues, Ana Filipa; Anton, Manuel; Giovanelli, Giorgio; Silva, Ana Maria

    2013-10-01

    Monitoring of atmospheric compounds at high latitudes is a key factor for a better understanding of the processes driving the chemical cycles of ozone and related chemical species. In this frame, the GASCOD (Gas Analizer Spectrometer Correlating Optical Differences) equipment is installed at the Mario Zucchelli Station (MZS - 74.69S, 164.12E) since December 1995, carrying out observations of nitrogen dioxide (NO2) and ozone (O3). The recent advances in sensor technologies and processor capabilities, suggested the setup of a new equipment, based on the same optical layout of the 'old' GASCOD , with enhanced performances and improved capabilities for the measurements of solar radiation in the UV-visible spectral range (300-700nm). The efforts accomplished, allowed for the increase of the investigated tracers. Actually, mainly due to the enlargement of the covered spectral range and to the adoption of a CCD sensor, in addition to the NO2 and O3 compounds, others species can be monitored with the new instrumental setup such as bromine, chlorine and iodine oxides (BrO, OClO and IO). The innovative equipment called GASCODNG (GASCOD New Generation) was installed at MZS during the 2012/2013 Italian Antarctic expedition, in the framework of the research projects SAMOA (Automatic Station Monitoring Antarctic Ozonosphere) and MATAGRO (Monitoring Atmospheric Tracers in Antarctica with Ground Based Observations) funded by the Italian and Portuguese Antarctic programs respectively. In this paper a brief description of the new equipment is provided, highlighting the main improvements with regard to the 'old' one. Furthermore the full dataset (1996 - 2012) of NO2 total columns, obtained with the GASCOD installed at MZS, is compared with the data obtained with satellite borne equipments (GOME, SCIAMACHY, OMI and GOME2) and the main statistical parameters are analyzed and discussed in detail.

  7. Atmospheric nitrogen oxides (NO and NO2) at Dome C, East Antarctica, during the OPALE campaign

    NASA Astrophysics Data System (ADS)

    Frey, M. M.; Roscoe, H. K.; Kukui, A.; Savarino, J.; France, J. L.; King, M. D.; Legrand, M.; Preunkert, S.

    2015-07-01

    Mixing ratios of the atmospheric nitrogen oxides NO and NO2 were measured as part of the OPALE (Oxidant Production in Antarctic Lands & Export) campaign at Dome C, East Antarctica (75.1° S, 123.3° E, 3233 m), during December 2011 to January 2012. Profiles of NOx mixing ratios of the lower 100 m of the atmosphere confirm that, in contrast to the South Pole, air chemistry at Dome C is strongly influenced by large diurnal cycles in solar irradiance and a sudden collapse of the atmospheric boundary layer in the early evening. Depth profiles of mixing ratios in firn air suggest that the upper snowpack at Dome C holds a significant reservoir of photolytically produced NO2 and is a sink of gas-phase ozone (O3). First-time observations of bromine oxide (BrO) at Dome C show that mixing ratios of BrO near the ground are low, certainly less than 5 pptv, with higher levels in the free troposphere. Assuming steady state, observed mixing ratios of BrO and RO2 radicals are too low to explain the large NO2 : NO ratios found in ambient air, possibly indicating the existence of an unknown process contributing to the atmospheric chemistry of reactive nitrogen above the Antarctic Plateau. During 2011-2012, NOx mixing ratios and flux were larger than in 2009-2010, consistent with also larger surface O3 mixing ratios resulting from increased net O3 production. Large NOx mixing ratios at Dome C arise from a combination of continuous sunlight, shallow mixing height and significant NOx emissions by surface snow (FNOx). During 23 December 2011-12 January 2012, median FNOx was twice that during the same period in 2009-2010 due to significantly larger atmospheric turbulence and a slightly stronger snowpack source. A tripling of FNOx in December 2011 was largely due to changes in snowpack source strength caused primarily by changes in NO3- concentrations in the snow skin layer, and only to a secondary order by decrease of total column O3 and associated increase in NO3- photolysis rates. A

  8. High-resolution measurements from the airborne Atmospheric Nitrogen Dioxide Imager (ANDI)

    NASA Astrophysics Data System (ADS)

    Lawrence, J. P.; Anand, J. S.; Vande Hey, J. D.; Leigh, R. R.; Monks, P. S.; Leigh, R. J.

    2015-06-01

    Nitrogen Dioxide is both a primary pollutant with direct health effects and a key precursor of the secondary pollutant ozone. This paper reports on the development, characterisation and test flight of the Atmospheric Nitrogen Dioxide Imager (ANDI) remote sensing system. The ANDI system includes an imaging (UV)-vis grating spectrometer able to capture scattered sunlight spectra for the determination of tropospheric nitrogen dioxide (NO2) concentrations by way of DOAS slant column density and vertical column density measurements. Results are shown for an ANDI test flight over Leicester City in the UK. Retrieved NO2 columns at a surface resolution of 80 m x 20 m revealed hot spots in a series of locations around Leicester City, including road junctions, the train station, major car parks, areas of heavy industry, a nearby airport (East Midlands) and a power station (Ratcliffe-on-Soar). In the city centre the dominant source of NO2 emissions was identified as road traffic, contributing to a background concentration as well as producing localised hot spots. Quantitative analysis revealed a significant urban increment over the city centre which increased throughout the flight.

  9. High-resolution measurements from the airborne Atmospheric Nitrogen Dioxide Imager (ANDI)

    NASA Astrophysics Data System (ADS)

    Lawrence, J. P.; Anand, J. S.; Vande Hey, J. D.; White, J.; Leigh, R. R.; Monks, P. S.; Leigh, R. J.

    2015-11-01

    Nitrogen dioxide is both a primary pollutant with direct health effects and a key precursor of the secondary pollutant ozone. This paper reports on the development, characterisation and test flight of the Atmospheric Nitrogen Dioxide Imager (ANDI) remote sensing system. The ANDI system includes an imaging UV/Vis grating spectrometer able to capture scattered sunlight spectra for the determination of tropospheric nitrogen dioxide (NO2) concentrations by way of DOAS slant column density and vertical column density measurements. Results are shown for an ANDI test flight over Leicester City in the UK on a cloud-free winter day in February 2013. Retrieved NO2 columns gridded to a surface resolution of 80 m × 20 m revealed hotspots in a series of locations around Leicester City, including road junctions, the train station, major car parks, areas of heavy industry, a nearby airport (East Midlands) and a power station (Ratcliffe-on-Soar). In the city centre the dominant source of NO2 emissions was identified as road traffic, contributing to a background concentration as well as producing localised hotspots. Quantitative analysis revealed a significant urban increment over the city centre which increased throughout the flight.

  10. Low Energy, Low Emissions: Sulfur Dioxide; Nitrogen Oxides, and Carbon Dioxide in Western Europe.

    ERIC Educational Resources Information Center

    Alcamo, Joseph; De Vries, Bert

    1992-01-01

    Links proposed low-energy scenarios for different Western European countries with the amount of pollutants that may result from these scenarios. Sulfur dioxide, nitrogen oxide, and carbon dioxide emissions are calculated for the 10 countries for which low-energy scenarios are available, resulting in reductions of 54%, 37%, and 40%, respectively.…

  11. Dual photon effects in nitrogen dioxide photolysis

    NASA Technical Reports Server (NTRS)

    Hakala, D.; Harteck, P.; Reeves, R. R.

    1974-01-01

    A previous study demonstrated two-photon consecutive absorption as being the most probable mechanism for the photodissociation of NO2 using a pulsed ruby laser at 6943 A. Additional data discussed here confirmed this and also examined an associated phenomenon, that of multiphoton induced fluorescence. The dissociation of NO2 by ON-O bond cleavage requires 3.4 eV, while the laser energy corresponds to 1.785 eV. The pooling of the energy of two photons would give more than enough energy to dissociate the NO2 into NO + O. Several mechanisms including (1) simultaneous absorption of two photons; (2) reaction of two singly excited NO2; (3) reaction of a singly excited NO2 with a ground state NO2; and (4) consecutive absorption of two photons were examined.

  12. Chemical modification of a porous silicon surface induced by nitrogen dioxide adsorption.

    PubMed

    Sharov, Constantine S; Konstantinova, Elizaveta A; Osminkina, Lyubov A; Timoshenko, Victor Yu; Kashkarov, Pavel K

    2005-03-17

    The effect of gaseous and liquid nitrogen dioxide on the composition and electronic properties of porous silicon (PS) is investigated by means of optical spectroscopy and electron paramagnetic resonance. It is detected that the interaction process is weak and strong forms of chemisorption on the PS surface, and the process may be regarded as an actual chemical reaction between PS and NO(2). It is found that NO(2) adsorption consists in forming different surface nitrogen-containing molecular groups and dangling bonds of Si atoms (P(b)-centers) as well as in oxidizing and hydrating the PS surface. Also observed are the formation of ionic complexes of P(b)-centers with NO(2) molecules and the generation of free charge carriers (holes) in the volume of silicon nanocrystals forming PS. PMID:16851549

  13. Atmospheric nitrogen oxides (NO and NO2) at Dome C, East Antarctica, during the OPALE campaign

    NASA Astrophysics Data System (ADS)

    Frey, M. M.; Roscoe, H. K.; Kukui, A.; Savarino, J.; France, J. L.; King, M. D.; Legrand, M.; Preunkert, S.

    2014-12-01

    Mixing ratios of the atmospheric nitrogen oxides NO and NO2 were measured as part of the OPALE (Oxidant Production in Antarctic Lands & Export) campaign at Dome C, East Antarctica (75.1° S, 123.3° E, 3233 m), during December 2011 to January 2012. Profiles of NOx mixing ratios of the lower 100 m of the atmosphere confirm that, in contrast to South Pole, air chemistry at Dome C is dominated by strong diurnal cycles in solar irradiance and atmospheric stability. Depth profiles of mixing ratios in firn air suggest that the upper snowpack at Dome C holds a significant reservoir of photolytically produced NO2 and is a sink of gas phase ozone (O3). First-time observations of BrO at Dome C suggest 2-3 pptv near the ground, with higher levels in the free troposphere. Assuming steady-state, observed mixing ratios of BrO and RO2 radicals are too low to explain the large NO2 : NO ratios found in ambient air. A previously not considered interference with pernitric acid (HNO4) may explain part of this inconsistency. During 2011-2012 NOx mixing ratios and flux were larger than in 2009-2010 consistent with also larger surface O3 mixing ratios resulting from increased net O3 production. Large NOx mixing ratios arose from a combination of changes in mixing height and NOx snow emission flux FNOx. During 23 December 2011-12 January 2012 median FNOx was twice that during the same period in 2009-2010 due to significantly larger atmospheric turbulence and a slightly stronger snowpack source. A tripling of FNOx in December 2011 was largely due to changes in snow pack source strength caused primarily by changes in NO3- concentrations in the snow skin layer, and only to a secondary order by decrease of total column O3 and associated increase in NO3- photolysis rates. Systematic changes in the quantum yield of NO3- photolysis over time may contribute to the observed FNOx variability.

  14. Abrupt recent trend changes in atmospheric nitrogen dioxide over the Middle East.

    PubMed

    Lelieveld, Jos; Beirle, Steffen; Hörmann, Christoph; Stenchikov, Georgiy; Wagner, Thomas

    2015-08-01

    Nitrogen oxides, released from fossil fuel use and other combustion processes, affect air quality and climate. From the mid-1990s onward, nitrogen dioxide (NO2) has been monitored from space, and since 2004 with relatively high spatial resolution by the Ozone Monitoring Instrument. Strong upward NO2 trends have been observed over South and East Asia and the Middle East, in particular over major cities. We show, however, that a combination of air quality control and political factors, including economical crisis and armed conflict, has drastically altered the emission landscape of nitrogen oxides in the Middle East. Large changes, including trend reversals, have occurred since about 2010 that could not have been predicted and therefore are at odds with emission scenarios used in projections of air pollution and climate change in the early 21st century. PMID:26601240

  15. Abrupt recent trend changes in atmospheric nitrogen dioxide over the Middle East

    PubMed Central

    Lelieveld, Jos; Beirle, Steffen; Hörmann, Christoph; Stenchikov, Georgiy; Wagner, Thomas

    2015-01-01

    Nitrogen oxides, released from fossil fuel use and other combustion processes, affect air quality and climate. From the mid-1990s onward, nitrogen dioxide (NO2) has been monitored from space, and since 2004 with relatively high spatial resolution by the Ozone Monitoring Instrument. Strong upward NO2 trends have been observed over South and East Asia and the Middle East, in particular over major cities. We show, however, that a combination of air quality control and political factors, including economical crisis and armed conflict, has drastically altered the emission landscape of nitrogen oxides in the Middle East. Large changes, including trend reversals, have occurred since about 2010 that could not have been predicted and therefore are at odds with emission scenarios used in projections of air pollution and climate change in the early 21st century. PMID:26601240

  16. Control of Nitrogen Dioxide in Stack Emission by Reaction with Ammonia

    NASA Technical Reports Server (NTRS)

    Metzler, A. J.; Stevenson, E. F.

    1970-01-01

    The development of an acid base gas-phase reaction system which utilizes anhydrous ammonia as the reactant to remove nitrogen dioxide from hydrazine-nitrogen tetroxide rocket combustion exhaust is reported. This reaction reduced NO2 levels in exhaust emissions so that the resulting stack emission is completely white instead of the earlier observed typical reddish-brown coloration. Preliminary analyses indicate the importance of reaction time and ammonia concentration on removal efficiency and elimination of the health hazard to individuals with respiratory problems.

  17. Ozone and nitrogen dioxide changes in the stratosphere during 1979-84

    NASA Technical Reports Server (NTRS)

    Callis, Linwood B.; Natarajan, Murali

    1986-01-01

    Analyses of stratospheric nitrogen dioxide distributions as measured by four different satellite experiments indicate midlatitude increases of up to 75 percent during the 1979-84 period. These increases are attributed to enhanced upper atmospheric formation of odd nitrogen during solar cycle 21 with downward transport to the stratosphere. The increases in NO2 provide an explanation for the recently observed dramatic springtime minima in the Antarctic ozone and suggest the reason for the reported midlatitude stratospheric ozone decreases observed by satellite and ground-based stations since the mid 1970s.

  18. NITROGEN DIOXIDE, PULMONARY FUNCTION, AND RESPIRATORY DISEASE

    EPA Science Inventory

    Concern as to the toxicity of the oxides of nitrogen has been frequently expressed in clinical and toxicological literature. Oxides of nitrogen are highly reactive compounds and suggest toxic effects on biological systems. The earliest evidence for potential damage to man occurre...

  19. Review of the Primary National Ambient Air Quality Standards for Nitrogen Dioxide: Risk and Exposure Assessment Planning Document

    EPA Science Inventory

    The U.S. Environmental Protection Agency (EPA) is conducting a review of the air quality criteria and the primary (health-based) national ambient air quality standards (NAAQS) for nitrogen dioxide (NO2). The major phases of the process for reviewing NAAQS include the following: (...

  20. INFLUENCE OF EXPOSURE PATTERNS OF NITROGEN DIOXIDE AND MODIFICATIONS BY OZONE ON SUSCEPTIBILITY TO BACTERIAL INFECTIOUS DISEASE IN MICE

    EPA Science Inventory

    The nitrogen dioxide (NO2) diurnal cycle found in urban communities usually consists of a low basal concentration upon which are superimposed higher concentration peaks or spikes of short duration. Various components of the environmental exposure mode were examined to assess effe...

  1. COMPARISON OF BIOCHEMICAL EFFECTS OF NITROGEN DIOXIDE, OZONE AND THEIR COMBINATION IN MOUSE LUNG. 1. INTERMITTENT EXPOSURES

    EPA Science Inventory

    Swiss Webster mice were exposed to either 4.8 ppm (9024 micrograms/cu.m.) nitrogen dioxide (NO2), 0.45 ppm (882 micrograms/cu.m.) ozone (O3), or their combination intermittently (8 hr daily) for 7 days, and the effects were studied in the lung by a series of physical and biochemi...

  2. Elevated NH 3 and NO 2 air concentrations and nitrogen deposition rates in the vicinity of a highway in Southern Bavaria

    NASA Astrophysics Data System (ADS)

    Kirchner, Manfred; Jakobi, Gert; Feicht, Ernst; Bernhardt, Markus; Fischer, Anton

    A transect study consisting of air concentration and deposition measurements of nitrogen compounds was performed to estimate the potential influence of car emissions on the nitrogen input to ecosystems. Therefore, two transects each consisting of 4 plots, the first in a coniferous forest and the second one in an extensively farmed grassland, were installed perpendicular to a highway south of Munich (Bavaria). Both profiles were influenced mainly by car emissions and showed only small local influences caused by agricultural activities. In the framework of a pilot study based upon denuder measurements we found a strong temporal dependency of both nitrogen dioxide (NO 2) and ammonia (NH 3) concentrations on traffic density. In the main study air concentrations of NO 2 and NH 3 were measured by passive samplers; they used as the basis for the estimation of dry deposition. These estimations have been compared with the results of analyses from simultaneously conducted canopy throughfall deposition and open air bulk measurements of nitrate (NO 3-) and ammonium (NH 4+). Additionally, within the forest transect the variety of different soil vegetation species was recorded and quantified. We obtained a strong gradient of gas concentrations along both profiles. Whereas the bulk deposition remained quite constant along the non-forested transect, the nitrogen throughfall deposition rate diminished substantially with the distance from the highway. The deposition rate at the forest edge was twice of that inside. The nitrogen load estimated for the examined forest in the vicinity of the highway was comparable to other forest ecosystems situated near diffuse emission sources from agriculture. It could be shown that changes in soil composition and soil vegetation along the forest transect are caused by decreasing nitrogen deposition with distance from the highway. The application of road salt in winter leads to further impacts.

  3. An intercomparison of airborne nitrogen dioxide instruments

    NASA Technical Reports Server (NTRS)

    Gregory, G. L.; Hoell, J. M., Jr.; Carroll, M. A.; Ridley, B. A.; Davis, D. D.; Bradshaw, J.; Rodgers, M. O.; Sandholm, S. T.; Schiff, H. I.; Torres, A. L.

    1990-01-01

    Results on NO2 instruments are reported from the NASA Global Tropospheric Experiment Chemical Instrumentation Test and Evaluation 2 (CITE 2) program in summer 1986. The instruments tested were (1) a two-photon LIF system using a laser for NO2-NO photolysis, (2) a chemiluminescence (CL) detector using FeSO4 for NO2-NO conversion, (3) a CL detector using an arc lamp for NO2-NO photolysis, and (4) a tunable-laser-diode multipath-absorption system. The procedures for the CITE 2 ground-based and flight tests are described in detail, and the results are presented in extensive graphs. Instrument (2) was eliminated because the FeSO4 converted atmospheric PAN to NO, resulting in spuriously high NO2 values. The remaining instruments gave readings in 30-40-percent agreement at NO2 mixing ratios of 100-200 parts per trillion by volume (pptv). At ratios below 50 pptv, the correlation among the measurements was very poor, with a tendency for system (4) to give higher values than (1) or (3).

  4. The impact of ClNO2 production on tropospheric nitrogen oxides and oxidants in a global model

    NASA Astrophysics Data System (ADS)

    Brown, S. S.; Saiz-Lopez, A.; Lamarque, J. F.; Kinnison, D. E.; Lopez-Hilfiker, F.; Thornton, J. A.; Jaegle, L.; Fibiger, D. L.; McDuffie, E. E.

    2015-12-01

    Heterogeneous uptake of dinitrogen pentoxide, N2O5, to aerosol is one of the most important reactions controlling the global budget of nitrogen oxides, with subsequent impacts on oxidants such as ozone and hydroxyl radical. Nearly all global chemical models assume that this uptake proceeds through hydrolysis to produce nitric acid, effectively a terminal sink for nitrogen oxides. However, recent field studies have shown that the yield of nitryl chloride, ClNO2, from N2O5 uptake is significant in many locations. Because ClNO2 photolyzes subsequent to its nighttime production to recycle NO2 and produce atomic chlorine, a potent oxidant, the impact of heterogeneous N2O5 uptake and the role of ClNO2 on the scale and distribution of oxidants need to be re-assessed. Here we present simulations using CAM-Chem incorporating halogen chemistry (tropospheric and stratospheric, including geographic and time varying VSLs precursor emissions) along with different assumptions for the magnitude and spatial distribution of ClNO2 yields from N2O5. The model shows the largest effects of ClNO2 production on tropospheric ozone during northern hemisphere late winter and early spring. Simulations are compared to observations from recent field campaigns, including ClNO2 and N2O5 from the Wintertime INvestigation of Transport, Emissions and Reactivity (WINTER) study on the NSF / NCAR C-130 aircraft on the U.S. East Coast in February and March of 2015.

  5. Exogenous sodium sulfide improves morphological and physiological responses of a hybrid Populus species to nitrogen dioxide.

    PubMed

    Hu, Yanbo; Bellaloui, Nacer; Sun, Guangyu; Tigabu, Mulualem; Wang, Jinghong

    2014-06-15

    Gaseous nitrogen dioxide (NO2) can disturb normal plant growth and trigger complex physiological responses. NO2-induced responses are influenced by biotic or abiotic factors. In this study, we investigated the effects of exogenous sodium sulfide (Na2S, 5mmolL(-1)) on epidermis and stomata related physico-chemical responses of hybrid poplar cuttings (Pouplus alba×P. berolinensis) to gaseous NO2 (4μl1(-1)) for three time periods (0, 14 and 48h). We also investigated hydrogen sulfide (H2S), nitrate-nitrogen and nitrate reductase activity (NR) in control and Na2S treated plants. Our results showed that NO2 exposure for 48h led to the decline of NR, maximal PSII quantum yield (Fv/Fm), net photosynthetic rate (Pn), and dark respiration rate (Rd). The maximum rate for the post-illumination carbon dioxide burst (PIB) occurred in 48-h exposed leaves 13-15s after darkening. Moreover, NO2 exposure resulted in a significant increase in nitrogen percentage (from 0 to 33%) and a decrease in the macro and micro-elements of leaf surface. Spraying Na2S aqueous solution on the leaf surfaces significantly increased the thicknesses of palisade/spongy tissue and H2S content. Na2S pretreatment alleviated NO2-caused toxic effects as indicated by increased NR and higher values of Pn, Fv/Fm, and actual photochemical efficiency in light (ФPSII) compared with the control. Na2S pretreatment had no significant impacts on PIB-based photorespiration or elements composition of a leaf surface. PMID:24635903

  6. Effects of nitrogen dioxide exposure on pulmonary function and airway reactivity in normal humans.

    PubMed

    Frampton, M W; Morrow, P E; Cox, C; Gibb, F R; Speers, D M; Utell, M J

    1991-03-01

    Nitrogen dioxide (NO2) is a product of combustion that has become recognized as a significant component of indoor air in some homes. Despite extensive study, it remains unresolved whether exposures to low levels of NO2 affect airway function or reactivity. These studies were designed to assess effects of various levels and patterns of NO2 exposure on pulmonary function and airway reactivity in normal humans. Normal volunteers screened for the absence of airway hyperreactivity were exposed for 3 h in an environmental chamber to purified air or NO2, separated by at least 2 wk, according to three protocols: (1) continuous 0.60 ppm NO2, (2) baseline 0.05 ppm NO2 with intermittent peaks of 2.0 ppm, and (3) continuous 1.5 ppm NO2. Subjects exercised for 10 min of each 30 min at a level sufficient to result in a minute ventilation near 40 L/min. Pulmonary function was measured before, during, and after exposure. Airway reactivity to increasing doses of carbachol was assessed 30 min after exposure. NO2 did not directly alter pulmonary function in any of the exposure protocols. In addition, airway reactivity was not altered by continuous exposure to 0.60 ppm or intermittent peaks of 2.0 ppm NO2. In contrast, continuous exposure to 1.5 ppm NO2 resulted in a greater fall in FVC and FEV1 in response to carbachol than after exposure to air (percent decrease in FVC: 1.5% after air, 3.9% after NO2, p less than 0.01). We conclude that for subjects without airway hyperreactivity, exposure to 1.5 ppm NO2 for 3 h increases airway reactivity, whereas repeated 15-min exposures to 2.0 ppm NO2 do not alter airway reactivity. PMID:2001061

  7. Nitrogen Dioxide Total Column Over Terra Nova Bay Station - Antarctica - During 2001

    NASA Astrophysics Data System (ADS)

    Bortoli, D.; Ravegnani, F.; Giovanelli, G.; Petritoli, A.; Kostadinov, I.

    GASCOD (Gas Analyzer Spectrometer Correlating Optical Differences), installed at the Italian Antarctic Station of Terra Nova Bay (TNB) - 74.69S, 164.12E - since 1995, carried out a full dataset of zenith scattered light measurements for the year 2001. The application of DOAS methodology to the collected data gave as final results, the slant column values for nitrogen dioxide. The seasonal variation shows a maxi- mum in the summer and it is in good agreement with the results obtained by other authors. The data analysis is performed by using different parameters like the po- tential vorticity (PV) at 500 K and the atmospheric temperatures at the same level. After the verification of the linear dependency between the NO2 slant column values and the temperature of NO2 cross section utilized in the DOAS algorithm, the actual stratospheric temperatures (from ECMWF) over TNB are applied to the results. The sensible changes in the nitrogen dioxide slant column values allow to highlight the good matching between the NO2 AM/PM ratio and the potential vorticity at 500 K. The NO2 slant column values follow the variations of the stratospheric temperature mainly during the spring season, when the lowest temperatures are observed and the ozone-hole phenomena mainly occur. ACKNOWLEDGMENTS: The author Daniele Bortoli was financially supported by the "Subprograma Ciência e Tecnologia do Ter- ceiro Quadro Comunitário de Apoio". The National Program for Antarctic Research (PNRA) supported this research.

  8. 40 CFR 52.728 - Control strategy: Nitrogen dioxide. [Reserved

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 3 2012-07-01 2012-07-01 false Control strategy: Nitrogen dioxide. 52.728 Section 52.728 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Illinois> § 52.728 Control strategy:...

  9. 40 CFR 52.728 - Control strategy: Nitrogen dioxide. [Reserved

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 3 2010-07-01 2010-07-01 false Control strategy: Nitrogen dioxide. 52.728 Section 52.728 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Illinois> § 52.728 Control strategy:...

  10. 40 CFR 52.728 - Control strategy: Nitrogen dioxide. [Reserved

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 3 2014-07-01 2014-07-01 false Control strategy: Nitrogen dioxide. 52.728 Section 52.728 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Illinois> § 52.728 Control strategy:...

  11. 40 CFR 52.728 - Control strategy: Nitrogen dioxide. [Reserved

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 3 2011-07-01 2011-07-01 false Control strategy: Nitrogen dioxide. 52.728 Section 52.728 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Illinois> § 52.728 Control strategy:...

  12. 40 CFR 52.728 - Control strategy: Nitrogen dioxide. [Reserved

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 3 2013-07-01 2013-07-01 false Control strategy: Nitrogen dioxide. 52.728 Section 52.728 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Illinois> § 52.728 Control strategy:...

  13. Continuous analysis of nitrogen dioxide in gas streams of plants

    NASA Technical Reports Server (NTRS)

    Durkin, W. T.; Kispert, R. C.

    1969-01-01

    Analyzer and sampling system continuously monitors nitrogen dioxide concentrations in the feed and tail gas streams of a facility recovering nitric acid. The system, using a direct calorimetric approach, makes use of readily available equipment and is flexible and reliable in operation.

  14. Validation of nitrogen dioxide measurements from the Improved Stratospheric and Mesospheric Sounder

    NASA Astrophysics Data System (ADS)

    Reburn, W. J.; Remedios, J. J.; Morris, P. E.; Rodgers, C. D.; Taylor, F. W.; Kerridge, B. J.; Knight, R. J.; Ballard, J.; Kumer, J. B.; Massie, S. T.

    1996-04-01

    Measurements of nitrogen dioxide (NO2) from the Improved Stratospheric and Mesospheric Sounder (ISAMS) on the Upper Atmosphere Research Satellite (UARS) are assessed. Channel 5 of the instrument was dedicated to observations of nitrogen dioxide and employed pressure-modulation and wideband radiometry to make measurements at 6.2 μm. This dual technique allows simultaneous determination of nitrogen dioxide mixing ratio and the aerosol extinction coefficient at this wavelength and therefore provides nitrogen dioxide data even in the presence of heavy aerosol loading. Approximately 180 days of data, in the period from September 1991 to July 1992, were obtained with, typically, over 2600 profiles per day for each retrieved species, covering an altitude range of 100-0.01 mbar. In this paper the version 10 data are assessed and a full error analysis is described. Comparisons with the Cryogenic Limb Array Etalon Spectrometer (CLAES) on UARS and the Limb Infrared Monitor of the Stratosphere (LIMS) on Nimbus 7 are also presented. It is concluded that the morphology of the retrieved ISAMS fields is robust and consistent with concurrent as well as previous infrared satellite measurements. Random errors are estimated to be of the order of 10% for nighttime and 15% for daytime NO2 near the maxima of the distributions, and systematic errors are estimated to be of a similar size. However, there remains an unresolved systematic difference of about a factor of 2 between ISAMS and CLAES. Both random and systematic errors are likely to be reduced in future versions of the processing.

  15. Improving spatial nitrogen dioxide prediction using diffusion tubes: A case study in West Central Scotland

    NASA Astrophysics Data System (ADS)

    Pannullo, Francesca; Lee, Duncan; Waclawski, Eugene; Leyland, Alastair H.

    2015-10-01

    It has been well documented that air pollution adversely affects health, and epidemiological pollution-health studies utilise pollution data from automatic monitors. However, these automatic monitors are small in number and hence spatially sparse, which does not allow an accurate representation of the spatial variation in pollution concentrations required for these epidemiological health studies. Nitrogen dioxide (NO2) diffusion tubes are also used to measure concentrations, and due to their lower cost compared to automatic monitors are much more prevalent. However, even combining both data sets still does not provide sufficient spatial coverage of NO2 for epidemiological studies, and modelled concentrations on a regular grid from atmospheric dispersion models are also available. This paper proposes the first modelling approach to using all three sources of NO2 data to make fine scale spatial predictions for use in epidemiological health studies. We propose a geostatistical fusion model that regresses combined NO2 concentrations from both automatic monitors and diffusion tubes against modelled NO2 concentrations from an atmospheric dispersion model in order to predict fine scale NO2 concentrations across our West Central Scotland study region. Our model exhibits a 47% improvement in fine scale spatial prediction of NO2 compared to using the automatic monitors alone, and we use it to predict NO2 concentrations across West Central Scotland in 2006.

  16. Nitrogen Dioxide pollution and hazardous household environment: what impacts more congenital malformations.

    PubMed

    Landau, D; Novack, L; Yitshak-Sade, M; Sarov, B; Kloog, I; Hershkovitz, R; Grotto, I; Karakis, I

    2015-11-01

    Nitrogen Dioxide (NO2) is a product of fuel combustion originating mainly from industry and transportation. Studies suggest an association between NO2 and congenital malformations (CM). We investigated an independent effect of NO2 on CM by adjusting to individual factors and household environment in 1024 Bedouin-Arab pregnant women in southern Israel. This population is characterised by high rates of CMs, frequent consanguineous marriages, paternal smoking, temporary housing and usage of open fire for heat cooking. Information on household risk factors was collected during an interview. Ambient measurements of 24-h average NO2 and meteorological conditions were obtained from 13 local monitors. Median value of daily NO2 measured in the area was 6.78ppb. CM was diagnosed in 8.0% (82) of offspring. Maternal NO2 exposure during the 1st trimester >8.6ppb was significantly associated with minor CM (RR=2.68, p=0.029). Major CM were independently associated with maternal juvenile diabetes (RR=9.97, p-value=0.002) and heating by open fire (RR=2.00, p-value=0.049), but not NO2 exposure. We found that NO2 emissions had an independent impact only on minor malformations, whereas major malformations depended mostly on the household environment. Antepartum deaths were associated by maternal morbidity. PMID:26171819

  17. 40 CFR 77.6 - Penalties for excess emissions of sulfur dioxide and nitrogen oxides.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... sulfur dioxide and nitrogen oxides. 77.6 Section 77.6 Protection of Environment ENVIRONMENTAL PROTECTION... sulfur dioxide and nitrogen oxides. (a)(1) If excess emissions of sulfur dioxide occur at the affected source or nitrogen oxide occur at an affected unit during any year, the owners and operators...

  18. 40 CFR 77.6 - Penalties for excess emissions of sulfur dioxide and nitrogen oxides.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... sulfur dioxide and nitrogen oxides. 77.6 Section 77.6 Protection of Environment ENVIRONMENTAL PROTECTION... sulfur dioxide and nitrogen oxides. (a)(1) If excess emissions of sulfur dioxide occur at the affected source or nitrogen oxide occur at an affected unit during any year, the owners and operators...

  19. 40 CFR 77.6 - Penalties for excess emissions of sulfur dioxide and nitrogen oxides.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... sulfur dioxide and nitrogen oxides. 77.6 Section 77.6 Protection of Environment ENVIRONMENTAL PROTECTION... sulfur dioxide and nitrogen oxides. (a)(1) If excess emissions of sulfur dioxide occur at the affected source or nitrogen oxide occur at an affected unit during any year, the owners and operators...

  20. Nitrogen dioxide distribution in street canyons

    NASA Astrophysics Data System (ADS)

    Laxen, Duncan P. H.; Noordally, Ehsan

    Weekly average NO 2 concentrations have been measured at over 40 locations within two canyonlike streets in central London, using passive diffusion tube samplers. A steady decline in concentrations with height is found, levels being close to local background at about 20 m. There is a rapid decline over the first 10-15 m horizontally from the centre of the road and concentrations are close to local background at a distance of 30 m. Concentrations are 10-15% higher close to traffic lights than they are 60 m upstream. Possible reasons for this are discussed. The results provide valuable information to assist in the selection of sites for chemiluminescence monitors, which are required to check compliance with the new European Council air quality standard for NO 2.

  1. Foliage plants for indoor removal of the primary combustion gases carbon monoxide and nitrogen dioxide

    NASA Technical Reports Server (NTRS)

    Wolverton, B. C.; Mcdonald, R. C.; Mesick, H. H.

    1985-01-01

    Foliage plants were evaluated for their ability to sorb carbon monoxide and nitrogen dioxide, the two primary gases produced during the combustion of fossil fuels and tobacco. The spider plant (Chlorophytum elatum var. vittatum) could sorb 2.86 micrograms CO/sq cm leaf surface in a 6 h photoperiod. The golden pothos (Scindapsus aureus) sorbed 0.98 micrograms CO/sq cm leaf surface in the same time period. In a system with the spider plant, greater than or equal to 99 percent of an initial concentration of 47 ppm NO2 could be removed in 6 h from a void volume of approximately 0.35 cu m. One spider plant potted in a 3.8 liter container can sorb 3300 micrograms CO and effect the removal of 8500 micrograms NO2/hour, recognizing the fact that a significant fraction of NO2 at high concentrations will be lost by surface sorption, dissolving in moisture, etc.

  2. Influence of photolysis on multispectral photoacoustic measurement of nitrogen dioxide concentration.

    PubMed

    Tian, Guoxun; Moosmüller, Hans; Arnott, W Patrick

    2013-09-01

    Multispectral photoacoustic instruments are commonly used to measure aerosol and nitrogen dioxide (NO2) light absorption coefficients to determine the radiation budget of the atmosphere. Here a new photoacoustic system is developed to explore the effect of photolysis on the measured signal in a multispectral photoacoustic spectrometer In this system, a 405-nm laser is used primarily as light source for photolysis. Additionally, a well-overlapped 532-nm laser, modulated at the resonant frequency of the photoacoustic instrument, is used to probe the NO2 concentration. As a result, the photolysis effect at 405 nm can be observed by the photoacoustic instrument through the 532-nm laser. This work determines an 11% reduction of the photoacoustic signal caused by the photolysis effect for typical conditions, which needs to be taken into account when calibrating multispectral photoacoustic spectrometers with NO2. PMID:24151684

  3. Concurrent multiaxis differential optical absorption spectroscopy system for the measurement of tropospheric nitrogen dioxide.

    PubMed

    Leigh, Roland J; Corlett, Gary K; Friess, Udo; Monks, Paul S

    2006-10-01

    The development of a new concurrent multiaxis (CMAX) sky viewing spectrometer to monitor rapidly changing urban concentrations of nitrogen dioxide is detailed. The CMAX differential optical absorption spectroscopy (DOAS) technique involves simultaneous spectral imaging of the zenith and off-axis measurements of spatially resolved scattered sunlight. Trace-gas amounts are retrieved from the measured spectra using the established DOAS technique. The potential of the CMAX DOAS technique to derive information on rapidly changing concentrations and the spatial distribution of NO2 in an urban environment is demonstrated. Three example data sets are presented from measurements during 2004 of tropospheric NO2 over Leicester, UK (52.62 degrees N, 1.12 degrees W). The data demonstrate the current capabilities and future potential of the CMAX DOAS method in terms of the ability to measure real-time spatially disaggregated urban NO2. PMID:16983440

  4. Ice hockey lung – a case of mass nitrogen dioxide poisoning in the Czech Republic

    PubMed Central

    Brat, Kristian; Merta, Zdenek; Plutinsky, Marek; Skrickova, Jana; Ing, Miroslav Stanek

    2013-01-01

    Nitrogen dioxide (NO2) is a toxic gas, a product of combustion in malfunctioning ice-resurfacing machines. NO2 poisoning is rare but potentially lethal. The authors report a case of mass NO2 poisoning involving 15 amateur ice hockey players in the Czech Republic. All players were treated in the Department of Respiratory Diseases at Brno University Hospital in November 2010 – three as inpatients because they developed pneumonitis. All patients were followed-up until November 2011. Complete recovery in all but one patient was achieved by December 2010. None of the 15 patients developed asthma-like disease or chronic cough. Corticosteroids appeared to be useful in treatment. Electric-powered ice-resurfacing machines are preferable in indoor ice skating arenas. PMID:24032121

  5. Spin coated unsubstituted copper phthalocyanine thin films for nitrogen dioxide sensors

    NASA Astrophysics Data System (ADS)

    Chakane, Sanjay; Datir, Ashok; Koinkar, Pankaj

    2015-03-01

    Copper phthalocyanine (CuPc) is synthesized chemically and used for making CuPc thin films using spin coating technique. Films were prepared from trifluroacetic acid (TFA) and chlorobenzene mixed solution on the glass substrate. Spin coated films of unsubstituted CuPc films were heat annealed at 150°C for 2 h duration and were used to study NO2 gas sensing characteristics. α-phase of CuPc is noted by UV-visible absorption spectra. IR spectra of undoped CuPc films and doped CuPc films with NO2 revealed that, doping of nitrogen dioxide modifies and deletes some of the bands. The effect of NO2 at various concentrations from 50 ppm to 500 ppm in atmospheric air at room temperature on the electrical conductivity of CuPc films was studied. Sensitivity, response time and repeatability of the CuPc sensor were discussed in this paper.

  6. Increase in tropospheric nitrogen dioxide over China observed from space.

    PubMed

    Richter, Andreas; Burrows, John P; Nüss, Hendrik; Granier, Claire; Niemeier, Ulrike

    2005-09-01

    Emissions from fossil fuel combustion and biomass burning reduce local air quality and affect global tropospheric chemistry. Nitrogen oxides are emitted by all combustion processes and play a key part in the photochemically induced catalytic production of ozone, which results in summer smog and has increased levels of tropospheric ozone globally. Release of nitrogen oxide also results in nitric acid deposition, and--at least locally--increases radiative forcing effects due to the absorption of downward propagating visible light. Nitrogen oxide concentrations in many industrialized countries are expected to decrease, but rapid economic development has the potential to increase significantly the emissions of nitrogen oxides in parts of Asia. Here we present the tropospheric column amounts of nitrogen dioxide retrieved from two satellite instruments GOME and SCIAMACHY over the years 1996-2004. We find substantial reductions in nitrogen dioxide concentrations over some areas of Europe and the USA, but a highly significant increase of about 50 per cent-with an accelerating trend in annual growth rate-over the industrial areas of China, more than recent bottom-up inventories suggest. PMID:16136141

  7. Boosting sensitivity of boron nitride nanotube (BNNT) to nitrogen dioxide by Fe encapsulation.

    PubMed

    Zhang, Yu-qing; Liu, Yue-Jie; Liu, Yan-ling; Zhao, Jing-xiang

    2014-06-01

    The pristine boron nitride nanotube (BNNT) exhibits a poor chemical reactivity to some adsorbates, thus greatly limiting its application for the gas sensor. In the present work, using density functional theory (DFT) methods, we put forward a novel strategy to enhance the sensitivity of BNNT to nitrogen dioxide (NO2) by the encapsulation of a single Fe atom inside its cavity. The results suggest that the NO2 molecule can be only physically adsorbed on the pristine BNNT with a small adsorption energy (-0.10 eV). After the inclusion of the Fe atom inside BNNT (Fe@BNNT), the interaction of NO2 molecules with this tube is significantly enhanced, leading to a transformation from the physisorption of on pristine BNNT to the current chemisorption. Interestingly, up to five NO2 molecules can be adsorbed on this encapsulated BNNT along its circumference with the average adsorption energy of -0.52 eV, corresponding to a short recovery time (6 ms). Moreover, 0.38 electrons are transferred from the Fe@BNNT to the adsorbed NO2 molecules, which is enough to induce the obvious change of its electrical conductance. Thus, we predict that the encapsulation of Fe atom inside BNNT would greatly boosts its sensitivity to NO2 molecules, indicating its potential application as NO2 sensors. PMID:24837498

  8. Sources of variation for indoor nitrogen dioxide in rural residences of Ethiopia

    PubMed Central

    2009-01-01

    Background Unprocessed biomass fuel is the primary source of indoor air pollution (IAP) in developing countries. The use of biomass fuel has been linked with acute respiratory infections. This study assesses sources of variations associated with the level of indoor nitrogen dioxide (NO2). Materials and methods This study examines household factors affecting the level of indoor pollution by measuring NO2. Repeated measurements of NO2 were made using a passive diffusive sampler. A Saltzman colorimetric method using a spectrometer calibrated at 540 nm was employed to analyze the mass of NO2 on the collection filter that was then subjected to a mass transfer equation to calculate the level of NO2 for the 24 hours of sampling duration. Structured questionnaire was used to collect data on fuel use characteristics. Data entry and cleaning was done in EPI INFO version 6.04, while data was analyzed using SPSS version 15.0. Analysis of variance, multiple linear regression and linear mixed model were used to isolate determining factors contributing to the variation of NO2 concentration. Results A total of 17,215 air samples were fully analyzed during the study period. Wood and crop were principal source of household energy. Biomass fuel characteristics were strongly related to indoor NO2 concentration in one-way analysis of variance. There was variation in repeated measurements of indoor NO2 over time. In a linear mixed model regression analysis, highland setting, wet season, cooking, use of fire events at least twice a day, frequency of cooked food items, and interaction between ecology and season were predictors of indoor NO2 concentration. The volume of the housing unit and the presence of kitchen showed little relevance in the level of NO2 concentration. Conclusion Agro-ecology, season, purpose of fire events, frequency of fire activities, frequency of cooking and physical conditions of housing are predictors of NO2 concentration. Improved kitchen conditions and

  9. Quantifying the impact of nitric oxide calibration gas mixture oxidation on reported nitrogen dioxide concentrations

    NASA Astrophysics Data System (ADS)

    Sweeney, Bryan P.; Quincey, Paul G.; Green, David; Fuller, Gary W.

    2015-03-01

    Chemiluminescent analysers for measuring nitric oxide (NO) and nitrogen dioxide (NO2) in ambient air are generally calibrated with certified gas standard cylinders of NO in nitrogen. Verification of the NOx and NO amount fractions has been carried out on many such 'on-site' calibration cylinders at air quality monitoring stations. These measurements indicate that significant numbers of these gas mixtures have become somewhat degraded, with several percent of the NO oxidised to NO2. The effect of not compensating for this degradation on reported concentrations is discussed. If such degradation is not quantified and corrected for, there will be a systematic under-reporting of NO2 concentrations, which, due to the non-linearity of the effect, could reduce high reported NO2 concentrations at kerbside sites by around 20%. This could significantly reduce the number of reported exceedances of the NO2 limit value at such sites, compared to results obtained where there is no degradation of the NO cylinder.

  10. Passive dosimeters for nitrogen dioxide in personal/indoor air sampling: A review

    PubMed Central

    Yu, Chang Ho; Morandi, Maria T.; Weisel, Clifford P.

    2015-01-01

    Accurate measurement of nitrogen dioxide concentrations in both outdoor and indoor environments, including personal exposures, is a fundamental step for linking atmospheric nitrogen dioxide levels to potential health and ecological effects. The measurement has been conducted generally in two ways: active (pumped) sampling and passive (diffusive) sampling. Diffusion samplers, initially developed and used for workplace air monitoring, have been found to be useful and cost-effective alternatives to conventional pumped samplers for monitoring ambient, indoor and personal exposures at the lower concentrations found in environmental settings. Since the 1970s, passive samplers have been deployed for ambient air monitoring in urban and rural sites, and to determine personal and indoor exposure to NO2. This article reviews the development of NO2 passive samplers, the sampling characteristics of passive samplers currently available, and their application in ambient and indoor air monitoring and personal exposure studies. The limitations and advantages of the various passive sampler geometries (i.e., tube, badge, and radial type) are also discussed. This review provides researchers and risk assessors with practical information about NO2 passive samplers, especially useful when designing field sampling strategies for exposure and indoor/outdoor air sampling. PMID:18446185

  11. Global modelling of the ClNO2 production impact on tropospheric nitrogen oxides and main oxidants

    NASA Astrophysics Data System (ADS)

    Cuevas Rodríguez, Carlos Alberto; Brown, Steven S.; Lamarque, Jean-Francoise; Saiz-Lopez, Alfonso; Kinnison, Douglas E.; Lopez-Hilfiker, Felipe; Thornton, Joel A.; Jaegle, Lyatt; Fibiger, Dorothy; McDuffie, Erin E.; Sullivan, Amy P.; Weber, Rodney J.; Dibb, Jack

    2016-04-01

    Heterogeneous uptake of dinitrogen pentoxide, N2O5, to aerosol is one of the most important reactions controlling the global budget of nitrogen oxides, with subsequent impacts on oxidants such as ozone and hydroxyl radical. Most chemistry global models assume that this uptake proceeds through hydrolysis to produce nitric acid, effectively a terminal sink for nitrogen oxides. However, recent field studies have shown that the yield of nitryl chloride, ClNO2, from N2O5 uptake is significant in many locations. Because ClNO2 photolyzes subsequent to its nighttime production to recycle NO2 and produce atomic chlorine, a potent oxidant, the impact of heterogeneous N2O5 uptake and the role of ClNO2 on the scale distribution of oxidants need to be re-assessed. Here we present global simulations using the chemistry-climate model CAM-Chem, including a state of the art halogen chemistry scheme and different assumptions for the magnitude and spatial distribution of ClNO2 yields from N2O5. The model shows a significant effect of ClNO2 production on tropospheric ozone, hydroxyl radical and peroxyacyl nitrates (PAN) during northern hemisphere late winter and early spring. Simulations are compared to observations from recent field campaigns, including ClNO2 and N2O5 from the Wintertime INvestigation of Transport, Emissions and Reactivity (WINTER) study on the NSF / NCAR C-130 aircraft on the U.S. East Coast in February and March of 2015.

  12. Evaluation of doped phthalocyanines and a chemically-sensitive field effect transistor for detecting nitrogen dioxide

    NASA Astrophysics Data System (ADS)

    Jenkins, Thomas J.

    1989-12-01

    The design and fabrication of an integrated circuit microsensor for the detection of nitrogen dioxide is examined. Metal-doped phthalocyanine compounds were evaluated as a candidate chemically sensitive membrane, and their performance was compared with respect to sensitivity, reversibility, and specificity. The microsensor consisted of the integration of an array of 9 sensing elements with amplifiers, a reference amplifier, and an analog multiplexer. The 9 individual sensing elements used an interdigitated gate electrode field effect transistor (IGEFET) coupled to a serially connected pair of inverting amplifiers using metal oxide semiconductor field effect transistors(MOSFETs). The interdigitated gate electrodes were coated with thin films of cobalt (II) phthalocyanine (CoPc), copper phthalocyanine (CuPc), lead phthalocyanine (PbPc), nickel (II) phthalocyanine (NiPc), and (undoped) phthalocyanine (Pc). An excitation signal was applied to the integrated circuit, and the multiplexed electrical response was measured in the time-domain and the frequency-domain. The electrical response was evaluated upon exposure to 20-, 80-, and 320-ppb of nitrogen dioxide (NO2) and diisopropyl methylphosphonate (DIMP) using filtered room air (less than 5 percent relative humidity) as the diluent. The electrical response was evaluated for film thickness of approximately 1500 A and 500 A. The rank ordering of the sensitivity of the materials to nitrogen dioxide from the most to least sensitive was: CoPc, NiPc, CuPc, PbPc, and then (undoped) Pc.

  13. Improved spectral fitting of nitrogen dioxide from OMI in the 405-465 nm window

    NASA Astrophysics Data System (ADS)

    van Geffen, J. H. G. M.; Boersma, K. F.; Van Roozendael, M.; Hendrick, F.; Mahieu, E.; De Smedt, I.; Sneep, M.; Veefkind, J. P.

    2015-04-01

    An improved nitrogen dioxide (NO2) slant column density retrieval for the Ozone Monitoring Instrument (OMI) in the 405-465 nm spectral region is presented. Since the launch of OMI on board NASA's EOS-Aura satellite in 2004, differential optical absorption spectroscopy (DOAS) retrievals of NO2 slant column densities have been the starting point for the KNMI DOMINO and NASA SP NO2 vertical column data as well as the OMI NO2 data of some other institutes. However, recent intercomparisons between NO2 retrievals from OMI and other UV/Vis and limb spectrometers, as well as ground-based measurements, suggest that OMI stratospheric NO2 is biased high. This study revises and, for the first time, fully documents the OMI NO2 retrieval in detail. The representation of the OMI slit function to convolve high-resolution reference spectra onto the relevant spectral grid is improved. The window used for the wavelength calibration is optimised, leading to much-reduced fitting errors. Ozone and water vapour spectra used in the fit are updated, reflecting the recently improved knowledge of their absorption cross section in the literature. The improved spectral fit also accounts for absorption by the O2-O2 collision complex and by liquid water over clear-water areas. The main changes in the improved spectral fitting result from the updates related to the wavelength calibration: the RMS error of the fit is reduced by 23% and the NO2 slant column by 0.85 × 1015 molec cm-2, independent of latitude, solar zenith angle and NO2 value. Including O2-O2 and liquid water absorption and updating the O3 and water vapour cross-section spectra further reduces NO2 slant columns on average by 0.35 × 1015 molec cm-2, accompanied by a further 9% reduction in the RMS error of the fit. The improved OMI NO2 slant columns are consistent with independent NO2 retrievals from other instruments to within a range that can be explained by photochemically driven diurnal increases in stratospheric NO2 and by

  14. Nitrate transporters in leaves and their potential roles in foliar uptake of nitrogen dioxide.

    PubMed

    Hu, Yanbo; Fernández, Victoria; Ma, Ling

    2014-01-01

    While plant roots are specialized organs for the uptake and transport of water and nutrients, the absorption of gaseous or liquid mineral elements by aerial plant parts has been recognized since more than one century. Nitrogen (N) is an essential macronutrient which generally absorbed either as nitrate (NO(-) 3) or ammonium (NH(+) 4) by plant roots. Gaseous nitrogen pollutants like N dioxide (NO2) can also be absorbed by plant surfaces and assimilated via the NO(-) 3 assimilation pathway. The subsequent NO(-) 3 flux may induce or repress the expression of various NO(-) 3-responsive genes encoding for instance, the transmembrane transporters, NO(-) 3/NO(-) 2 (nitrite) reductase, or assimilatory enzymes involved in N metabolism. Based on the existing information, the aim of this review was to theoretically analyze the potential link between foliar NO2 absorption and N transport and metabolism. For such purpose, an overview of the state of knowledge on the NO(-) 3 transporter genes identified in leaves or shoots of various species and their roles for NO(-) 3 transport across the tonoplast and plasma membrane, in addition to the process of phloem loading is briefly provided. It is assumed that a NO2-induced accumulation of NO(-) 3/NO(-) 2 may alter the expression of such genes, hence linking transmembrane NO(-) 3 transporters and foliar uptake of NO2. It is likely that NRT1/NRT2 gene expression and species-dependent apoplastic buffer capacity may be also related to the species-specific foliar NO2 uptake process. It is concluded that further work focusing on the expression of NRT1 (NRT1.1, NRT1.7, NRT1.11, and NRT1.12), NRT2 (NRT2.1, NRT2.4, and NRT2.5) and chloride channel family genes (CLCa and CLCd) may help us elucidate the physiological and metabolic response of plants fumigated with NO2. PMID:25126090

  15. Effect of carbon monoxide and nitrogen dioxide on ICR mice

    NASA Technical Reports Server (NTRS)

    Hilado, C. J.; Cumming, H. J.

    1977-01-01

    Times to incapacitation and death and LC(50) values were determined for male ICR mice exposed to different concentration of carbon monoxide for 30 min and of nitrogen dioxide for 10 min in a 4.2 liter hemispherical chamber. The data indicate that ICR mice are more resistant to these two toxicants than Swiss albino mice. The carbon monoxide LC(50) for a 30-min exposure was about 8,000 ppm for ICR mice compared to 3,570 ppm for Swiss albino mice. The nitrogen dioxide LC(50) for a 10-min exposure was above 2,000 ppm for ICR mice compared to about 1,000 ppm for Swiss albino mice.

  16. Uptake rate of nitrogen dioxide by potato plants

    SciTech Connect

    Sinn, J.P.; Pell, E.J.; Kabel, R.L.

    1984-06-01

    Greenhouse-grown potato plants were exposed to nitrogen dioxide in an exposure chamber to determine the rate of NO/sub 2/ uptake at concentrations from 228 to 817 ..mu..g/m/sup 3/ (0.12-0.43 ppm). Results show that a consistent increase in uptake rate accompanied an increase in NO/sub 2/ exposure concentrations. Exposure in the range of concentration had no significant effect on leaf diffusive resistance.

  17. Curing preceramic polymers by exposure to nitrogen dioxide

    NASA Technical Reports Server (NTRS)

    Rabe, James A. (Inventor); Lipowitz, Jonathan (Inventor); Lu, Paul P. (Inventor)

    1991-01-01

    A rapid method of infusibilizing (curing) preceramic polymers comprising treatment said polymers with gaseous nitrogen dioxide. The infusibilized polymers may be pyrolyzed to temperatures in excess of about 800.degree. C. to yield ceramic materials with low oxygen content and, thus, good thermal stability. The methods are especially useful for the production of ceramic fibers and, more specifically, to the on-line production of ceramic fibers.

  18. Repeated Nitrogen Dioxide Exposures and Eosinophilic Airway Inflammation in Asthmatics: A Randomized Crossover Study

    PubMed Central

    Guillossou, Gaëlle; Neukirch, Catherine; Dehoux, Monique; Koscielny, Serge; Bonay, Marcel; Cabanes, Pierre-André; Samet, Jonathan M.; Mure, Patrick; Ropert, Luc; Tokarek, Sandra; Lambrozo, Jacques; Aubier, Michel

    2014-01-01

    Background: Nitrogen dioxide (NO2), a ubiquitous atmospheric pollutant, may enhance the asthmatic response to allergens through eosinophilic activation in the airways. However, the effect of NO2 on inflammation without allergen exposure is poorly studied. Objectives: We investigated whether repeated peaks of NO2, at various realistic concentrations, induce changes in airway inflammation in asthmatics. Methods: Nineteen nonsmokers with asthma were exposed at rest in a double-blind, crossover study, in randomized order, to 200 ppb NO2, 600 ppb NO2, or clean air once for 30 min on day 1 and twice for 30 min on day 2. The three series of exposures were separated by 2 weeks. The inflammatory response in sputum was measured 6 hr (day 1), 32 hr (day 2), and 48 hr (day 3) after the first exposure, and compared with baseline values measured twice 10–30 days before the first exposure. Results: Compared with baseline measurements, the percentage of eosinophils in sputum increased by 57% after exposure to 600 ppb NO2 (p = 0.003) but did not change significantly after exposure to 200 ppb. The slope of the association between the percentage of eosinophils and NO2 exposure level was significant (p = 0.04). Eosinophil cationic protein in sputum was highly correlated with eosinophil count and increased significantly after exposure to 600 ppb NO2 (p = 0.001). Lung function, which was assessed daily, was not affected by NO2 exposure. Conclusions: We observed that repeated peak exposures of NO2 performed without allergen exposure were associated with airway eosinophilic inflammation in asthmatics in a dose-related manner. Citation: Ezratty V, Guillossou G, Neukirch C, Dehoux M, Koscielny S, Bonay M, Cabanes PA, Samet JM, Mure P, Ropert L, Tokarek S, Lambrozo J, Aubier M. 2014. Repeated nitrogen dioxide exposures and eosinophilic airway inflammation in asthmatics: a randomized crossover study. Environ Health Perspect 122:850–855; http://dx.doi.org/10.1289/ehp.1307240 PMID

  19. The effect of nitrogen dioxide on particle formation during ozonolysis of two abundant monoterpenes indoors

    NASA Astrophysics Data System (ADS)

    Nøjgaard, Jacob Klenø; Bilde, Merete; Stenby, Charlotte; Nielsen, Ole John; Wolkoff, Peder

    The effect of the nitrogen dioxide (NO 2) concentration on particle formation during ozonolysis of two abundant monoterpenes indoors, α-pinene and d-limonene, was studied in dry air in 1000 l Tedlar bags at 21±2 °C and ambient pressure. Particle size distributions were measured during 1 h after the reaction was initiated. In mixtures of 50 parts per billion volume (ppbv) of monoterpene and 50 ppbv of ozone (O 3), d-limonene produced about five times as many particles (10-350 nm) as α-pinene after 60 min. The presence of NO 2 introduced an additional loss term for O 3, resulting in formation of the nitrate radical. This affected particle formation, since the nucleation potential of NO 3 is much lower than O 3. Modeling showed that the observed decrease in particle concentration from d-limonene/O 3/NO 2 mixtures was likely to be ascribed to the O 3/NO 2 reaction at NO 2 concentrations <150 ppb, above which unknown mechanisms additionally reduced the particle formation. In similar experiments with α-pinene, the particle concentration and volume were substantially reduced in the presence of NO 2, e.g. 162 ppbv NO 2 reduced the particle number concentration by a factor of 10. In addition, the detection of particle formation was delayed as the NO 2 concentration increased, but the additional loss of O 3 in the O 3/NO 2 reaction could not explain the observation. The particle mode progressively increased with the NO 2 concentration for both monoterpenes. Oxidation of d-limonene may be highly relevant for new particle formation in indoor air, whereas ozonolysis products of α-pinene seem less likely to nucleate in indoor environments.

  20. Associations between daily mortality in London and combined oxidant capacity, ozone and nitrogen dioxide.

    PubMed

    Williams, M L; Atkinson, R W; Anderson, H R; Kelly, F J

    2014-01-01

    Both nitrogen dioxide (NO2) and ozone (O3) are powerful oxidants in ambient air that are intimately linked through atmospheric chemistry and which continuously interchange over very short timescales. Based upon atmospheric chemistry alone, there is a strong, a priori, reason for considering O3 and NO2 together in epidemiological studies, rather than either of the two pollutants separately in single-pollutant models. This paper compares two approaches to this, using Ox, defined as O3 + NO2, as a single metric and also using O3 and NO2 together in two-pollutant models. We hypothesised that the magnitude of the association between Ox and daily mortality would be greater than for NO2 and O3 individually. Using collocated hourly measurements for O3 and NO2 in London, from 2000 to 2005, we carried out a time series analysis of daily mortality. We investigated O3, NO2 and Ox individually in single-pollutant Poisson regression models and NO2 and O3 jointly in two-pollutant models in both all-year and season-specific analyses. We observed larger associations for mean 24-h concentrations of Ox (1.30 % increase in mortality per 10 ppb) than for O3 (0.87 %) and NO2 (0 %) individually. However, when analysed jointly in two-pollutant models, associations for O3 (1.54 %) and NO2 (1.07 %) were comparable to the Ox association. Season-specific analyses broadly followed this pattern irrespective of whether the Ox concentrations were driven by O3 production (summer) or depletion (winter). This novel approach in air pollution epidemiology captures the simultaneous impact of both oxidants whilst avoiding many of the statistical issues associated with two-pollutant models and potentially simplifies health impact calculations. PMID:25431629

  1. Investigation of the Nitrogen Dioxide Pollution in Urban Areas using a New Portable ICAD Instrument

    NASA Astrophysics Data System (ADS)

    Horbanski, Martin; Pöhler, Denis; Adler, Tim; Lampel, Johannes; Kanatschnig, Florian; Oesterle, Tobias; Reh, Miriam; Platt, Ulrich

    2016-04-01

    Nitrogen oxides (NOx) and especially nitrogen dioxide (NO2), are still among of the most problematic pollutants in urban areas not only in developing, but also in industrialized countries. Despite the measures taken to reduce their emissions, NO2 concentrations in many urban areas exceed the WHO recommended limits of 40 μg/m3 for annual mean and 200 μg/m3 for 1 hour mean. Additionally it is known that the NO2 concentration in urban areas has a strong spatial and temporal variability, due to the large number of NOx emitting point sources (mainly traffic) found in densely populated areas. However, the layout of air monitoring networks in most urban areas, installed to continuously monitor the officially prescribed NO2 limits, does not reflect the high spatial variability because they only conduct measurements at a single or few selected sampling points, mainly on major roads, which are often not representative for the whole urban area. At present these uncertainties about the spatial NO2 distribution constitute severe limitations for the assessment of health risks, for the quality of chemical model calculations, and for developing effective measures to reduce NOx emissions. We developed a new light-weight and portable ICAD (Iterative Cavity Enhanced DOAS) instrument which detects NO2 at a detection limit as low as 0.2 μg/m3 with a high time resolution of seconds. The instrument is based on the Cavity Enhanced (CE-) DOAS technique, which directly identifies and quantifies NO2 by its differential optical absorption. Therefore, it does not suffer from interferences by other trace gas species like O3 or NOy. This is a great advantage over other NO2 instruments (e.g. solid state detectors or chemiluminescence instruments). We present the result of ICAD NO2 measurements, which we recently performed in more than 10 German cities. The ICAD instrument was mounted on mobile platforms like cars and bicycles, measuring the NO2 concentrations along carefully selected tracks

  2. Improved spectral fitting of nitrogen dioxide from OMI in the 405-465 nm window

    NASA Astrophysics Data System (ADS)

    van Geffen, J. H. G. M.; Boersma, K. F.; Van Roozendael, M.; Hendrick, F.; Mahieu, E.; De Smedt, I.; Sneep, M.; Veefkind, J. P.

    2014-10-01

    An improved nitrogen dioxide (NO2) slant column density retrieval for the Ozone Monitoring Instrument (OMI) in the 405-465 nm spectral region is presented. Since the launch of OMI on board NASA's EOS-Aura satellite in 2004, DOAS retrievals of NO2 slant column densities have been the starting point for the KNMI DOMINO (v2.0) and NASA SP (v2.1) retrievals. However, recent intercomparisons between NO2 retrievals from OMI and other UV/Vis and limb spectrometers, as well as ground-based measurements, clearly suggested that OMI stratospheric NO2 is biased high. This study revises the OMI NO2 retrieval in detail. The representation of the OMI slit function to convolve high-resolution reference spectra onto the relevant spectral grid is improved. The window used for the wavelength calibration is optimised, leading to much-reduced fitting errors. Ozone and water vapour spectra used in the fit are updated, reflecting the recently improved knowledge on their absorption cross section as documented in the literature. The improved spectral fit also accounts for absorption by the O2-O2 collision complex and by liquid water over clear-water areas. The main changes in the improved spectral fitting result from the updates related to the wavelength calibration: the RMS error of the fit is reduced by 23% and the NO2 slant column by 0.85 × 1015 molec cm-2, independent of latitude, solar zenith angle and NO2 value. Including O2-O2 and liquid water absorption and updating the O3 and water vapour cross-section spectra further reduces NO2 slant columns on average by 0.35 × 1015 molec cm-2, accompanied with a further 9% reduction in the RMS error of the fit. The improved OMI NO2 slant columns are consistent with independent NO2 retrievals to within a range that can be explained by photo-chemically driven diurnal increases in stratospheric NO2 and by small differences in fitting window and fitting approach. The revisions indicate that current OMI NO2 slant columns suffered mostly from an

  3. Nitrogen uptake by wheat seedlings, interactive effects of four nitrogen sources: NO3-, NO2-, NH4+, and urea

    NASA Technical Reports Server (NTRS)

    Criddle, R. S.; Ward, M. R.; Huffaker, R. C.

    1988-01-01

    The net influx (uptake) rates of NO3-, NH4+, NO2-, and urea into roots of wheat (Triticum aestivum cv Yecora Rojo) seedlings from complete nutrient solutions containing all four compounds were monitored simultaneously. Although urea uptake was too slow to monitor, its presence had major inhibitory effects on the uptake of each of the other compounds. Rates of NO3-, NH4+, and NO2- uptake depended in a complex fashion on the concentration of all four N compounds. Equations were developed which describe the uptake rates of each of the compounds, and of total N, as functions of concentrations of all N sources. Contour plots of the results show the interactions over the range of concentrations employed. The coefficients of these equations provide quantitative values for evaluating primary and interactive effects of each compound on N uptake.

  4. 40 CFR 52.230 - Control strategy and regulations: Nitrogen dioxide.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...: Nitrogen dioxide. 52.230 Section 52.230 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Control strategy and regulations: Nitrogen dioxide. (a) The requirements of § 52.14(c)(3) of this chapter... nitrogen oxides emission reduction attainable through application of reasonably available...

  5. 40 CFR 52.230 - Control strategy and regulations: Nitrogen dioxide.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...: Nitrogen dioxide. 52.230 Section 52.230 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Control strategy and regulations: Nitrogen dioxide. (a) The requirements of § 52.14(c)(3) of this chapter... nitrogen oxides emission reduction attainable through application of reasonably available...

  6. 40 CFR 52.230 - Control strategy and regulations: Nitrogen dioxide.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...: Nitrogen dioxide. 52.230 Section 52.230 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Control strategy and regulations: Nitrogen dioxide. (a) The requirements of § 52.14(c)(3) of this chapter... nitrogen oxides emission reduction attainable through application of reasonably available...

  7. 40 CFR 52.230 - Control strategy and regulations: Nitrogen dioxide.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...: Nitrogen dioxide. 52.230 Section 52.230 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Control strategy and regulations: Nitrogen dioxide. (a) The requirements of § 52.14(c)(3) of this chapter... nitrogen oxides emission reduction attainable through application of reasonably available...

  8. Tropospheric nitrogen dioxide column retrieval based on ground-based zenith-sky DOAS observations

    NASA Astrophysics Data System (ADS)

    Tack, Frederik; Hendrick, Francois; Goutail, Florence; Fayt, Caroline; Merlaud, Alexis; Pinardi, Gaia; Pommereau, Jean-Pierre; Van Roozendael, Michel

    2014-05-01

    Nitrogen dioxide (NO2) is one of the most important chemically active trace gases in the troposphere. Listed as primary pollutant, it is also a key precursor in the formation of tropospheric ozone, aerosols, and acid rain, and can contribute locally to radiative forcing. The long-term monitoring of this species is therefore of great relevance. Here we present a new method to retrieve tropospheric NO2 vertical column amounts from ground-based zenith-sky measurements of scattered sunlight. It is based on a four-step approach consisting of (1) the DOAS analysis of zenith radiance spectra using a fixed reference spectrum corresponding to low tropospheric NO2 content, (2) the determination of the residual amount in the reference spectrum using a Langley-plot-type method, (3) the removal of the stratospheric content from the daytime total slant column using stratospheric vertical columns measured at twilight and simulated stratospheric NO2 diurnal variation, (4) estimation of the tropospheric vertical columns by dividing the resulting tropospheric slant columns by appropriate air mass factors. The retrieval algorithm is tested on a 2 month dataset acquired from June to July 2009 by the BIRA MAX-DOAS instrument in the framework of the Cabauw (51.97° N, 4.93° E) Intercomparison campaign for Nitrogen Dioxide measuring Instruments (CINDI). The tropospheric vertical column amounts derived from zenith-sky observations are compared to the vertical columns retrieved from the off-axis and direct-sun measurements of the same MAX-DOAS instrument as well as to data of a co-located SAOZ (Système d'Analyse par Observations Zénithales) spectrometer operated by LATMOS. First results show a good agreement between the different data sets with correlation coefficients and slopes close to or larger than 0.85. We observe that the main error sources arise from the uncertainties in the determination of the residual NO2 amount in the reference spectrum, the stratospheric NO2 abundance and

  9. Pulse radiolysis study of the reactions of catechins with nitrogen dioxide

    NASA Astrophysics Data System (ADS)

    Gebicki, Jerzy L.; Meisner, Piotr; Stawowska, Katarzyna; Gebicka, Lidia

    2012-12-01

    Nitrogen dioxide (•NO2), one of the oxidizing radicals formed in vivo is suspected to play a role in various pathophysiological processes. The reactions of •NO2 with dietary catechins, the group of flavonoids present in high amounts in green tea and red wine, have been investigated by pulse radiolysis method. The kinetics of the reaction of •NO2 with gallic acid have been also studied for comparison. The spectra of transient intermediates are presented. The rate constants of the reaction of •NO2 with catechin, epigallocatechin, epigallocatechin gallate and gallic acid determined by the competition method with 2,2'-azinobis-(3-ethylbenzthiazoline-6-sulfonate) at pH 7.0 and room temperature have been found to be 0.9, 1.0, 2.3 and 0.5×108 M-1 s-1, respectively. The values for catechins are among the highest reported for the reactions of •NO2 with non-radical compounds.

  10. Antioxidative Reaction of Carotenes against Peroxidation of Fatty Acids Initiated by Nitrogen Dioxide: A Theoretical Study.

    PubMed

    Chen, Shau-Jiun; Huang, Li-Yen; Hu, Ching-Han

    2015-07-30

    In this study, we investigated the antioxidative functions of carotenes (CARs) against the peroxidation of lipids initiated by nitrogen dioxide using density functional theory. The hydrogen-atom transfer (HAT), radical adduct formation (RAF), and electron transfer (ET) mechanisms were investigated. We chose β-carotene (β-CAR) and lycopene (LYC) and compared their NO2(•) initiations and peroxidations with those of linoleic acid (LAH), the model of the lipid. We found that for CARs ET is more likely to occur in the most polar (water) environment than are HAT and RAF. In less polar environments, CARs react more readily with NO2(•) via HAT and RAF than does the lipid model, LAH. Comparatively, reaction barriers for the RAF between CARs and NO2(•) are smaller than those for the HAT. The additions of O2 to the radical intermediates O2N-CAR(•) and CAR(-H)(•) involve sizable barriers and are endergonic. Other than HAT of LAH, we revealed that lipid peroxidation is likely to be initiated by -NO2 addition and the subsequent barrierless addition of O2. Finally, LYC is a more effective antioxidative agent against NO2(•)-initiated lipid peroxidation than is β-CAR. PMID:26106906

  11. Oxidation of diclofenac with chlorine dioxide in aquatic environments: influences of different nitrogenous species.

    PubMed

    Wang, Yingling; Liu, Haijin; Liu, Guoguang; Xie, Youhai; Ni, Tianjun

    2015-06-01

    The oxidation of diclofenac (DCF), a non-steroidal anti-inflammatory drug and emerging water pollutant, with chlorine dioxide was investigated under simulated water disinfection conditions. The reaction kinetics as functions of the initial concentrations of DCF, different nitrogenous species, and different pE values were experimentally determined. The results demonstrated that DCF reacted rapidly with ClO2, where more than 75 % of DCF (≤3.00 μM) was removed by 18.94 μM ClO2 within 60 s. All of the reactions followed pseudo first-order kinetics with respect to DCF, and the rate constant, k obs, exhibited a significant decrease from 4.21 × 10(-2) to 8.09 × 10(-3) s(-1), as the initial DCF concentration was increased from 1.00 to 5.00 μM. Furthermore, the degradation kinetics of DCF was clearly dependent on nitrogen-containing ion concentrations in the reaction solution. Ammonium and nitrite ions inhibited the DCF degradation by ClO2, whereas nitrate ion clearly initiated its promotion. In contrast, the inhibitory effect of NO2 (-) was more robust than that of NH4 (+). When the values of pE were gradually increased, the transformation of NH4 (+) to NO2 (-), and subsequently to NO3 (-), would occur, the rate constants were initially decreased, and then increased. When NH4 (+) and NO2 (-) coexisted, the inhibitory effect on the DCF degradation was less than the sum of the partial inhibitory effect. However, when NO2 (-) and NO3 (-) coexisted, the actual inhibition rate was greater than the theoretical estimate. These results indicated that the interaction of NH4 (+) and NO2 (-) was antagonistic, while the coexistence of NO2 (-) and NO3 (-) was observed to have a synergistic effect in aqueous environments. PMID:25604564

  12. Recent satellite-based trends of tropospheric nitrogen dioxide over large urban agglomerations worldwide

    NASA Astrophysics Data System (ADS)

    Schneider, P.; Lahoz, W. A.; van der A, R.

    2015-02-01

    Trends in tropospheric nitrogen dioxide (NO2) columns over 66 large urban agglomerations worldwide have been computed using data from the SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY) instrument onboard the Envisat platform for the period August 2002 to March 2012. A seasonal model including a~linear trend was fitted to the satellite-based time series over each site. The results indicate distinct spatial patterns in trends. While agglomerations in Europe, North America, and some locations in East Asia/Oceania show decreasing tropospheric NO2 levels on the order of -5% yr-1, rapidly increasing levels of tropospheric NO2 are found for agglomerations in large parts of Asia, Africa, and South America. The site with the most rapidly increasing absolute levels of tropospheric NO2 was found to be Tianjin in China with a trend of 3.04 (±0.47) × 1015 molecules cm-2yr-1, whereas the site with the most rapidly increasing relative trend was Kabul in Afghanistan with 14.3 (±2.2) % yr-1. In total, 34 sites exhibited increasing trends of tropospheric NO2 throughout the study period, 24 of which were found to be statistically significant. A total of 32 sites showed decreasing levels of tropospheric NO2 during the study period, of which 20 sites did so at statistically significant magnitudes. Overall, going beyond the relatively small set of megacities investigated previously, this study provides the first consistent analysis of recent changes in tropospheric NO2 levels over most large urban agglomerations worldwide, and indicates that changes in urban NO2 levels are subject to substantial regional differences as well as influenced by economic and demographic factors.

  13. Hydraulic studies of drilling microbores with supercritical steam, nitrogen and carbon dioxide

    DOE Data Explorer

    Ken Oglesby

    2010-01-01

    Hydraulic studies of drilling microbores at various depths and with various hole sizes, tubing, fluids and rates showed theoretical feasibility. WELLFLO SIMULATIONS REPORT STEP 4: DRILLING 10,000 FT WELLS WITH SUPERCRITICAL STEAM, NITROGEN AND CARBON DIOXIDE STEP 5: DRILLING 20,000 FT WELLS WITH SUPERCRITICAL STEAM, NITROGEN AND CARBON DIOXIDE STEP 6: DRILLING 30,000 FT WELLS WITH SUPERCRITICAL STEAM, NITROGEN AND CARBON DIOXIDE Mehmet Karaaslan, MSI

  14. Developmental and hematological responses to low level continuous exposure of nitrogen dioxide in mice

    NASA Technical Reports Server (NTRS)

    Singh, J.

    1977-01-01

    Young healthy mice were continuously exposed to 0ppm, 0.5ppm, 1.0ppm and 5ppm nitrogen dioxide gas for eight weeks. Nitrogen dioxide exposure for eight weeks decreased the average weight of mice, increased the average weight of lungs, heart, and brain and decreased the average weight of liver. Nitrogen dioxide exposure did not have any effects on the WBC and RBC in mice blood but it increased the HCT and HGB in mice blood. Nitrogen dioxide exposure increased the MCV and decreased the MCH and MCHC in mice blood.

  15. Nitrogen dioxide vapor penetration of chlorobutyl rubber SCAPE under operational conditions

    NASA Technical Reports Server (NTRS)

    Schehl, T. A.; Beall, T. W.

    1980-01-01

    Operational self contained atmospheric protective ensembles (SCAPE suits) and fabric from the suits were subjected to a series of tests designed to determine the amount of exposure a wearer of the suit would receive if a spill of the hypergolic oxidizer nitrogen tetroxide (N2O4) should occur nearby. The results of these tests show that a wearer of a "stock" SCAPE suit equipped with a standard liquid air pack, if exposed to a spill resulting in a 26 percent increase of oxidizer in the surrounding atmosphere, will experiment no detectable concentration of nitrogen dioxide (NO2) inside the suit for 15 minutes. Thereafter, the NO2 concentration within the suit will increase for 35 minutes at a rate of 0.07 ppm per minute and then at a gradually decreasing rate until an equilibrium concentration of 3.4 ppm is attained after 100 minutes. Momentary increases of as much as 1.6 ppm can be expected if the wearer were to rise quickly from a squatting position, but the additional NO2 would be dissipated within three minutes. The effect of liquid and vapor N2O4 and of liquid monomethylhydrazine on permeation rates and tensile strength of the SCAPE suit fabric was also investigated.

  16. Partial oxidation of methane to methanol with nitrogen dioxide in dielectric barrier discharge plasma: experimental and molecular modeling

    NASA Astrophysics Data System (ADS)

    Indarto, Antonius

    2016-04-01

    Non-catalytic conversion of methane (CH4) and nitrogen dioxide (NO2) into methanol (CH3OH) has been conducted and presented in this paper. Experiments were carried out using dielectric barrier discharge as the reaction medium in atmospheric pressure and temperature conditions. High yield production of methanol was achieved (18-20% mol) by single-stage plasma reaction with maximum selectivity of 32% mol. Compared to other oxidants, such as O2, the presence of NO2 in the plasma reaction resulted in higher methanol selectivity. For better understanding of the reactions, density functional theory calculations were also performed and discussed.

  17. Measurement of nitrogen dioxide in cigarette smoke using quantum cascade tunable infrared laser differential absorption spectroscopy (TILDAS)

    NASA Astrophysics Data System (ADS)

    Shorter, Joanne H.; Nelson, David D.; Zahniser, Mark S.; Parrish, Milton E.; Crawford, Danielle R.; Gee, Diane L.

    2006-04-01

    Although nitrogen dioxide (NO 2) has been previously reported to be present in cigarette smoke, the concentration estimates were derived from kinetic calculations or from measurements of aged smoke, where NO 2 was formed some time after the puff was taken. The objective of this work was to use tunable infrared laser differential absorption spectroscopy (TILDAS) equipped with a quantum cascade (QC) laser to determine if NO 2 could be detected and quantified in a fresh puff of cigarette smoke. A temporal resolution of ˜0.16 s allowed measurements to be taken directly as the NO 2 was formed during the puff. Sidestream cigarette smoke was sampled to determine if NO 2 could be detected using TILDAS. Experiments were conducted using 2R4F Kentucky Reference cigarettes with and without a Cambridge filter pad. NO 2 was detected only in the lighting puff of whole mainstream smoke (without a Cambridge filter pad), with no NO 2 detected in the subsequent puffs. The measurement precision was ˜1.0 ppbV Hz -1/2, which allows a detection limit of ˜0.2 ng in a 35 ml puff volume. More NO 2 was generated in the lighting puff using a match or blue flame lighter (29 ± 21 ng) than when using an electric lighter (9 ± 3 ng). In the presence of a Cambridge filter pad, NO 2 was observed in the gas phase mainstream smoke for every puff (total of 200 ± 30 ng/cigarette) and is most likely due to smoke chemistry taking place on the Cambridge filter pad during the smoke collection process. Nitrogen dioxide was observed continuously in the sidestream smoke starting with the lighting puff.

  18. Recent satellite-based trends of tropospheric nitrogen dioxide over large urban agglomerations worldwide

    NASA Astrophysics Data System (ADS)

    Schneider, P.; Lahoz, W. A.; van der A, R.

    2014-09-01

    Trends in tropospheric nitrogen dioxide (NO2) concentrations over 66 large urban agglomerations worldwide have been computed using data from the SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY) instrument onboard the Envisat platform for the period August 2002 to March 2012. A seasonal model including a linear trend was fitted to the satellite-based time series over each site. The results indicate distinct spatial patterns in trends. While agglomerations in Europe, North America, and some locations in East Asia/Oceania show decreasing tropospheric NO2 levels on the order of -5 % yr-1, rapidly increasing levels of tropospheric NO2 are found for agglomerations in large parts of Asia, Africa, and South America. The site with the most rapidly increasing absolute levels of tropospheric NO2 was found to be Tianjin in China with a trend value of 3.04 (±0.47) × 1015 molecules cm-2 yr-1, whereas the site with the most rapidly increasing relative trend was Kabul in Afghanistan with 14.3 (±2.2) % yr-1. In total, 34 sites exhibited increasing trends of tropospheric NO2 throughout the study period, 24 of which were found to be statistically significant. A total of 32 sites showed decreasing levels of tropospheric NO2 during the study period, of which 20 sites did so at statistically significant magnitudes. Overall, going beyond the relatively small set of megacities investigated previously, this study provides the first consistent analysis of recent changes in tropospheric NO2 levels over most large urban agglomerations worldwide.

  19. Isotopic composition of passively collected nitrogen dioxide emissions: Vehicle, soil and livestock source signatures

    NASA Astrophysics Data System (ADS)

    Felix, J. David; Elliott, Emily M.

    2014-08-01

    Quantifying contributions of local and regional NOx emission sources is an important initial step towards accurately assessing improvements in NOx emission reduction efforts. Current global NOx inventories report large uncertainties in contributions of some NOx sources, especially diffuse sources (e.g. lightning and soil NOx). Examining the isotopic composition of NOx and its oxidation products (NOy) is one approach to further constrain contributions from these sources. While natural and anthropogenically-derived NOx emissions are reported to have relatively distinct δ15N values that could aid NOx source apportionment studies, existing δ15N-NOx source data is limited and variable collection approaches have been employed. To build on existing δ15N-NOx source data, inexpensive and easily deployable passive samplers were used to collect nitrogen dioxide (NO2) emissions and its oxidation product, nitric acid (HNO3), from multiple emission sources including livestock waste, fertilized soils, and vehicles. The resulting isotope data provides evidence that passive samplers can be used across a range of environmental conditions with widely varying NO2 concentrations and NO2 isotopic compositions. Using this approach, we report the first δ15N and δ18O-NO2 of livestock waste emissions, as well as the first measurements of δ18O-NO2 from biogenic soil and vehicle emissions. We observe the highest δ15N-NO2 values to date of vehicle emissions and investigate potential fractionations associated with oxidation and equilibrium processes. The large differences reported here between δ15N-NO2 values from fossil fuel-based sources and microbially-produced sources allows for identification and possible quantification of source contributions to ambient NOx concentrations.

  20. Lung Cancer and Exposure to Nitrogen Dioxide and Traffic: A Systematic Review and Meta-Analysis

    PubMed Central

    Laden, Francine; Cohen, Aaron J.; Raaschou-Nielsen, Ole; Brauer, Michael; Loomis, Dana

    2015-01-01

    Background and objective Exposure to traffic-related air pollutants is an important public health issue. Here, we present a systematic review and meta-analysis of research examining the relationship of measures of nitrogen oxides (NOx) and of various measures of traffic-related air pollution exposure with lung cancer. Methods We conducted random-effects meta-analyses of studies examining exposure to nitrogen dioxide (NO2) and NOx and its association with lung cancer. We identified 20 studies that met inclusion criteria and provided information necessary to estimate the change in lung cancer per 10-μg/m3 increase in exposure to measured NO2. Further, we qualitatively assessed the evidence of association between distance to roadways and traffic volume associated with lung cancer. Results The meta-estimate for the change in lung cancer associated with a 10-μg/m3 increase in exposure to NO2 was 4% (95% CI: 1%, 8%). The meta-estimate for change in lung cancer associated with a 10-μg/m3 increase in NOx was similar and slightly more precise, 3% (95% CI: 1%, 5%). The NO2 meta-estimate was robust to different confounding adjustment sets as well as the exposure assessment techniques used. Trim-and-fill analyses suggest that if publication bias exists, the overall meta-estimate is biased away from the null. Forest plots for measures of traffic volume and distance to roadways largely suggest a modest increase in lung cancer risk. Conclusion We found consistent evidence of a relationship between NO2, as a proxy for traffic-sourced air pollution exposure, with lung cancer. Studies of lung cancer related to residential proximity to roadways and NOx also suggest increased risk, which may be attributable partly to air pollution exposure. The International Agency for Research on Cancer recently classified outdoor air pollution and particulate matter as carcinogenic (Group 1). These meta-analyses support this conclusion, drawing particular attention to traffic-sourced air

  1. Total Column Observation of Nitrogen Dioxide and Ozone in the Four Corners Region

    NASA Astrophysics Data System (ADS)

    Butterfield, Z.; Dubey, M.; Lindenmaier, R.; Herman, J. R.; Disterhoft, P.; Minschwaner, K.

    2013-12-01

    Nitrogen Dioxide (NO2) is a pollutant created by the burning of fossil fuels, which is intricately related to levels of ozone (O3), a tropospheric pollutant and greenhouse gas. Observing and understanding the behavior of these two chemicals in the atmosphere is essential to monitoring and verifying power plant emissions. In the Four Corners region, the San Juan and Four Corners power plants produce a total of 0.3 kilotonnes of NOX (combined Nitric Oxide (NO) and NO2) per day from burning fossil fuels. We compare NO2 column measurements from a ground-based solar spectrometer (Pandora) and from the satellite-based Ozone Monitoring Instrument (OMI). We also compare O3 column measurements obtained from Pandora and a Brewer Ozone Spectrophotometer. Using O3 profiles obtained with ozonesondes and by separating long and short time scale changes in total column measurements we isolate tropospheric ozone columns and explore their relationship with the troposphere-dominated total column measurements of NO2.

  2. Impact of titanium dioxide nanomaterials on nitrogen fixation rate and intracellular nitrogen storage in Anabaena variabilis.

    PubMed

    Cherchi, Carla; Gu, April Z

    2010-11-01

    This study comprehensively investigated the impact of titanium dioxide nanomaterials (nTiO(2)) exposure on cell growth, nitrogen fixation activity, and nitrogen storage dynamics in the primary producer cyanobacteria Anabaena variabilis at various dose concentrations and exposure time lengths. The results indicated that both growth rate (EC(50)-96 h of 0.62 mgTiO(2)/L) and nitrogen fixation activity (EC(50)-96 h of 0.4 mgTiO(2)/L) were inhibited by nTiO(2) exposure. The Hom's law (C(n)T(m)) was used as inactivation model to predict the concentration- and time-dependent inhibition of growth and nitrogen fixation activity. The kinetic parameters determined suggested that the time of exposure has a greater influence than the nTiO(2) concentration in toxicity. We observed, for the first time, that nTiO(2) induced a dose (concentration and time)-dependent increase in both the occurrence and intracellular levels of the nitrogen-rich cyanophycin grana proteins (CGPs). The results implied that CGPs may play an important role in the stress response mechanisms of nTiO(2) exposure and can serve as a toxicity assessment endpoint indicator. This study demonstrated that nitrogen-fixing activity could be hampered by the release of nTiO(2) in aquatic environments; therefore it potentially impacts important biogeochemical processes, such as carbon and nitrogen cycling. PMID:20853867

  3. MAPPING CRITICAL LEVELS OF OZONE, SULPHUR DIOXIDE AND NITROGEN DIOXIDE FOR CROPS, FORESTS AND NATURAL VEGETATION IN THE UNITED STATES

    EPA Science Inventory

    Air pollution abatement strategies for controlling nitrogen dioxide, sulfur dioxide, and ozone emissions in the United States focus on a "Standards-based" approach. his approach places limits on air pollution by maintaining a baseline value for air quality, no matter what the eco...

  4. The Cabauw Intercomparison Campaign for Nitrogen Dioxide Measuring Instruments (CINDI): Design, Execution, and Early Results

    NASA Technical Reports Server (NTRS)

    Piters, Ankie; Boersma, K.F.; Kroon, M.; Hains, J. C.; Roozendael, M. Van; Wittrock, F.; Abuhassan, N.; Adams, C.; Akrami, M.; Allaart, M. A. F.; Apituley, A.; Beirle, S.; Bergwerff, J. B.; Berkhout, A. J. C.; Brunner, D.; Cede, A.; Chong, J.; Clemer, K.; Fayt, C.; FrieB, U.; Gast, L. F. L.; Gil-Ojeda, M.; Goutail, F.; Graves, R.; Griesfeller, A.

    2012-01-01

    From June to July 2009 more than thirty different in-situ and remote sensing instruments from all over the world participated in the Cabauw Intercomparison campaign for Nitrogen Dioxide measuring Instruments (CINDI). The campaign took place at KNMI's Cabauw Experimental Site for Atmospheric Research (CESAR) in the Netherlands. Its main objectives were to determine the accuracy of state-ofthe- art ground-based measurement techniques for the detection of atmospheric nitrogen dioxide (both in-situ and remote sensing), and to investigate their usability in satellite data validation. The expected outcomes are recommendations regarding the operation and calibration of such instruments, retrieval settings, and observation strategies for the use in ground-based networks for air quality monitoring and satellite data validation. Twenty-four optical spectrometers participated in the campaign, of which twenty-one had the capability to scan different elevation angles consecutively, the so-called Multi-axis DOAS systems, thereby collecting vertical profile information, in particular for nitrogen dioxide and aerosol. Various in-situ samplers and lidar instruments simultaneously characterized the variability of atmospheric trace gases and the physical properties of aerosol particles. A large data set of continuous measurements of these atmospheric constituents has been collected under various meteorological conditions and air pollution levels. Together with the permanent measurement capability at the CESAR site characterizing the meteorological state of the atmosphere, the CINDI campaign provided a comprehensive observational data set of atmospheric constituents in a highly polluted region of the world during summertime. First detailed comparisons performed with the CINDI data show that slant column measurements of NO2, O4 and HCHO with MAX-DOAS agree within 5 to 15%, vertical profiles of NO2 derived from several independent instruments agree within 25% of one another, and MAX

  5. Associations of Cough Prevalence with Ambient Polycyclic Aromatic Hydrocarbons, Nitrogen and Sulphur Dioxide: A Longitudinal Study

    PubMed Central

    Anyenda, Enoch Olando; Higashi, Tomomi; Kambayashi, Yasuhiro; Nguyen, Thao Thi Thu; Michigami, Yoshimasa; Fujimura, Masaki; Hara, Johsuke; Tsujiguchi, Hiromasa; Kitaoka, Masami; Asakura, Hiroki; Hori, Daisuke; Yamada, Yohei; Hayashi, Koichiro; Hayakawa, Kazuichi; Nakamura, Hiroyuki

    2016-01-01

    Information on potential cough triggers including environmental irritants is vital for successful management of chronic cough in patients. We investigated the relationship between ambient levels of particulate polycyclic aromatic hydrocarbons (PAH), nitrogen dioxide (NO2) and sulphur dioxide (SO2) exposures with cough prevalence. Eighty-three adult patients, who had been physician diagnosed with at least asthma, cough variant asthma and/or atopic cough, were divided into asthma and non-asthma groups. They recorded daily cough symptoms during 4 January–30 June 2011 study period while daily samples of total suspended particles were simultaneously collected by use of glass fiber filters and the particulate PAH content determined by high performance liquid chromatography coupled with a fluorescence detector. Ambient concentrations of NO2 and SO2 were obtained from a local monitoring site. Logistic regression models using generalized estimating equations were used to determine population-averaged estimates of association between cough prevalence and ambient pollutant exposures for the two groups. Fully adjusted odds ratios from single pollutant models were 1.083 (95% confidence interval (CI): 1.029, 1.140) and 1.097 (95% CI: 1.016, 1.185) per 0.57 ng/m3 for lag2 PAH exposure, while only for asthma group had significant associations with NO2 and SO2 exposures for both lag2 and lag02. Similar associations were observed in multipollutant models. This finding suggests that ambient PAH, NO2, and SO2 exposure even at low levels is related to cough prevalence in adult chronic cough patients and may be considered as aggravating factor during clinical management of the condition. PMID:27517941

  6. Reactions of nitrogen oxides with heme models. Characterization of NO and NO2 dissociation from Fe(TPP)(NO2)(NO) by flash photolysis and rapid dilution techniques: Fe(TPP)(NO2) as an unstable intermediate.

    PubMed

    Lim, Mark D; Lorkovic, Ivan M; Wedeking, Katrin; Zanella, Andrew W; Works, Carmen F; Massick, Steve M; Ford, Peter C

    2002-08-21

    Described are studies directed toward elucidating the controversial chemistry relating to the solution phase reactions of nitric oxide with the iron(II) porphyrin complex Fe(TPP)(NO) (1, TPP = meso-tetraphenylporphinato2-). The only reaction observable with clean NO is the formation of the diamagnetic dinitrosyl species Fe(TPP)(NO)2 (2), and this is seen only at low temperatures (K(1) < 3 M(-1) at ambient temperature). However, 1 does readily react reversibly with N2O3 in the presence of excess NO to give the nitro nitrosyl complex Fe(TPP)(NO2)(NO) (3), suggesting that previous claims that 1 promotes NO disproportionation to give 3 may have been compromised by traces of air in the nitric oxide sources. It is also noted that 3 undergoes reversible loss of NO to give the elusive nitro species Fe(TPP)(NO2) (4), which has been implicated as a powerful oxygen atom transfer agent in reactions with various substrates. Furthermore, in the presence of excess NO2, the latter undergoes oxidation to the stable nitrato analogue Fe(TPP)(NO3) (5). Owing to such reactivity of Fe(TPP)(NO2), flash photolysis and stopped-flow kinetics rather than static techniques were necessary for the accurate measurement of dissociation equilibria characteristic of Fe(TPP)(NO2)(NO) in 298 K toluene solution. Flash photolysis of 3 resulted in competitive NO2 and NO dissociation to give Fe(TPP)(NO) and Fe(TPP)(NO2), respectively. The rate constant for the reaction of 1 with N2O3 to generate Fe(TPP)(NO2)(NO) was determined to be 1.8 x 10(6) M(-1) s(-1), and that for the NO reaction with 4 was similarly determined to be 4.2 x 10(5) M(-1) s(-1). Stopped-flow rapid dilution techniques were used to determine the rate constant for NO dissociation from 3 as 2.6 s(-1). The rapid dilution experiments also demonstrated that Fe(TPP)(NO2) readily undergoes further oxidation to give Fe(TPP)(NO3). The mechanistic implications of these observations are discussed, and it is suggested that NO2 liberated

  7. Development and optimization of a lab-on-a-chip device for the measurement of trace nitrogen dioxide gas in the atmosphere.

    PubMed

    Takabayashi, Yoshimasa; Uemoto, Michihisa; Aoki, Kenjiro; Odake, Tamao; Korenaga, Takashi

    2006-04-01

    We propose the use of lab-on-a-chip technology for measuring gaseous chemical pollutants, and describe the development of a microchip for the detection of nitrogen dioxide (NO2) in air. A microchip fabricated from quartz glass has been developed for handling the following three functions, gas absorption, chemical reaction and fluorescence detection. Channels constructed in the microchip were covered with porous glass plates, allowing nitrogen dioxide to penetrate into the triethanolamine (TEA) flowing within the microchannel beneath. The nitrogen dioxide was then mixed with TEA and reacted with a suitable fluorescence reagent in the chemical reaction chamber in the microchip. The reacted solution was then allowed to flow into the fluorescence detection area to be excited by an ultraviolet light-emitting diode (UV-LED), and the fluorescence was detected using a photomultiplier tube (PMT). The reaction time, reagent concentration, pH, flow rate and other measurement conditions were optimised for analysis of nitrogen dioxide in air. Preliminary studies with standardized test solutions revealed quantitative measurements of nitrite ion (NO2-), which corresponded to atmospheric nitrogen dioxide in the range of 10-80 ppbv. PMID:16568175

  8. Nitrogen fixation rate and chlorophyll content of the lichen Peltigera canina exposed to sulfur dioxide

    SciTech Connect

    Henriksson, E.; Pearson, L.C.

    1981-01-01

    In general, the rate of nitrogen fixation decreased when the lichen Peltigera canina (L.) Willd. was exposed to sulfur dioxide gas at levels from 0.1 to 500 ppm; at 30 ppm, however, nitrogen fixation was stimulated. The chlorophyll content decreased as the level of sulfur dioxide increased.

  9. 40 CFR 77.6 - Penalties for excess emissions of sulfur dioxide and nitrogen oxides.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 16 2011-07-01 2011-07-01 false Penalties for excess emissions of sulfur dioxide and nitrogen oxides. 77.6 Section 77.6 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) EXCESS EMISSIONS § 77.6 Penalties for excess emissions of sulfur dioxide and nitrogen oxides. (a)(1)...

  10. Tropospheric nitrogen dioxide column retrieval from ground-based zenith-sky DOAS observations

    NASA Astrophysics Data System (ADS)

    Tack, F.; Hendrick, F.; Goutail, F.; Fayt, C.; Merlaud, A.; Pinardi, G.; Hermans, C.; Pommereau, J.-P.; Van Roozendael, M.

    2015-06-01

    We present an algorithm for retrieving tropospheric nitrogen dioxide (NO2) vertical column densities (VCDs) from ground-based zenith-sky (ZS) measurements of scattered sunlight. The method is based on a four-step approach consisting of (1) the differential optical absorption spectroscopy (DOAS) analysis of ZS radiance spectra using a fixed reference spectrum corresponding to low NO2 absorption, (2) the determination of the residual amount in the reference spectrum using a Langley-plot-type method, (3) the removal of the stratospheric content from the daytime total measured slant column based on stratospheric VCDs measured at sunrise and sunset, and simulation of the rapid NO2 diurnal variation, (4) the retrieval of tropospheric VCDs by dividing the resulting tropospheric slant columns by appropriate air mass factors (AMFs). These steps are fully characterized and recommendations are given for each of them. The retrieval algorithm is applied on a ZS data set acquired with a multi-axis (MAX-) DOAS instrument during the Cabauw (51.97° N, 4.93° E, sea level) Intercomparison campaign for Nitrogen Dioxide measuring Instruments (CINDI) held from 10 June to 21 July 2009 in the Netherlands. A median value of 7.9 × 1015 molec cm-2 is found for the retrieved tropospheric NO2 VCDs, with maxima up to 6.0 × 1016 molec cm-2. The error budget assessment indicates that the overall error σTVCD on the column values is less than 28%. In the case of low tropospheric contribution, σTVCD is estimated to be around 39% and is dominated by uncertainties in the determination of the residual amount in the reference spectrum. For strong tropospheric pollution events, σTVCD drops to approximately 22% with the largest uncertainties on the determination of the stratospheric NO2 abundance and tropospheric AMFs. The tropospheric VCD amounts derived from ZS observations are compared to VCDs retrieved from off-axis and direct-sun measurements of the same MAX-DOAS instrument as well as to data

  11. Tropospheric nitrogen dioxide column retrieval from ground-based zenith-sky DOAS observations

    NASA Astrophysics Data System (ADS)

    Tack, F.; Hendrick, F.; Goutail, F.; Fayt, C.; Merlaud, A.; Pinardi, G.; Hermans, C.; Pommereau, J.-P.; Van Roozendael, M.

    2015-01-01

    We present an algorithm for retrieving tropospheric nitrogen dioxide (NO2) vertical column densities (VCDs) from ground-based zenith-sky (ZS) measurements of scattered sunlight. The method is based on a four-step approach consisting of (1) the Differential Optical Absorption Spectroscopy (DOAS) analysis of ZS radiance spectra using a fixed reference spectrum corresponding to low NO2 absorption, (2) the determination of the residual amount in the reference spectrum using a Langley-plot-type method, (3) the removal of the stratospheric content from the daytime total measured slant column based on stratospheric VCDs measured at sunrise and sunset, and simulation of the rapid NO2 diurnal variation, (4) the retrieval of tropospheric VCDs by dividing the resulting tropospheric slant columns by appropriate air mass factors (AMFs). These steps are fully characterized and recommendations are given for each of them. The retrieval algorithm is applied on a ZS dataset acquired with a Multi-AXis (MAX-) DOAS instrument during the Cabauw (51.97° N, 4.93° E, sea level) Intercomparison campaign for Nitrogen Dioxide measuring Instruments (CINDI) held from the 10 June to the 21 July 2009 in the Netherlands. A median value of 7.9 × 1015 molec cm-2 is found for the retrieved tropospheric NO2 VCDs, with maxima up to 6.0 × 1016 molec cm-2. The error budget assessment indicates that the overall error σTVCD on the column values is less than 28%. In case of low tropospheric contribution, σTVCD is estimated to be around 39% and is dominated by uncertainties in the determination of the residual amount in the reference spectrum. For strong tropospheric pollution events, σTVCD drops to approximately 22% with the largest uncertainties on the determination of the stratospheric NO2 abundance and tropospheric AMFs. The tropospheric VCD amounts derived from ZS observations are compared to VCDs retrieved from off-axis and direct-sun measurements of the same MAX-DOAS instrument as well as to

  12. Area-level socioeconomic deprivation, nitrogen dioxide exposure, and term birth weight in New York City.

    PubMed

    Shmool, Jessie L C; Bobb, Jennifer F; Ito, Kazuhiko; Elston, Beth; Savitz, David A; Ross, Zev; Matte, Thomas D; Johnson, Sarah; Dominici, Francesca; Clougherty, Jane E

    2015-10-01

    Numerous studies have linked air pollution with adverse birth outcomes, but relatively few have examined differential associations across the socioeconomic gradient. To evaluate interaction effects of gestational nitrogen dioxide (NO2) and area-level socioeconomic deprivation on fetal growth, we used: (1) highly spatially-resolved air pollution data from the New York City Community Air Survey (NYCCAS); and (2) spatially-stratified principle component analysis of census variables previously associated with birth outcomes to define area-level deprivation. New York City (NYC) hospital birth records for years 2008-2010 were restricted to full-term, singleton births to non-smoking mothers (n=243,853). We used generalized additive mixed models to examine the potentially non-linear interaction of nitrogen dioxide (NO2) and deprivation categories on birth weight (and estimated linear associations, for comparison), adjusting for individual-level socio-demographic characteristics and sensitivity testing adjustment for co-pollutant exposures. Estimated NO2 exposures were highest, and most varying, among mothers residing in the most-affluent census tracts, and lowest among mothers residing in mid-range deprivation tracts. In non-linear models, we found an inverse association between NO2 and birth weight in the least-deprived and most-deprived areas (p-values<0.001 and 0.05, respectively) but no association in the mid-range of deprivation (p=0.8). Likewise, in linear models, a 10 ppb increase in NO2 was associated with a decrease in birth weight among mothers in the least-deprived and most-deprived areas of -16.2g (95% CI: -21.9 to -10.5) and -11.0 g (95% CI: -22.8 to 0.9), respectively, and a non-significant change in the mid-range areas [β=0.5 g (95% CI: -7.7 to 8.7)]. Linear slopes in the most- and least-deprived quartiles differed from the mid-range (reference group) (p-values<0.001 and 0.09, respectively). The complex patterning in air pollution exposure and deprivation

  13. Dosimetry of ozone and nitrogen dioxide in man and animals

    SciTech Connect

    Overton, J.H. Jr.; Miller, F.J.

    1984-01-01

    The health effects of ozone (O/sub 3/) and nitrogen dioxide (NO/sub 2/) are assessed from animal toxicological, controlled human, and epidemiological studies. These assessments will be strengthened when results of animal studies can be quantitatively extrapolated to man. To achieve quantitative extrapolation, improvements are needed in the areas of dosimetry and species sensitivity. And, of course, an adequate health effect data base must exist on which to make extrapolations. The focus of this paper is to review the regional dosimetry of O/sub 3/ and NO/sub 2/ in the respiratory tract of man and animals. Dosimetry relates to estimating the amount of pollutant reaching a specific target region of the respiratory tract as a function of exposure concentration. At present, there are two approaches to dosimetry, experimental and mathematical modeling, which are discussed.

  14. Evaluation of Land Use Regression Models for Nitrogen Dioxide and Benzene in Four US Cities

    PubMed Central

    Mukerjee, Shaibal; Smith, Luther; Neas, Lucas; Norris, Gary

    2012-01-01

    Spatial analysis studies have included the application of land use regression models (LURs) for health and air quality assessments. Recent LUR studies have collected nitrogen dioxide (NO2) and volatile organic compounds (VOCs) using passive samplers at urban air monitoring networks in El Paso and Dallas, TX, Detroit, MI, and Cleveland, OH to assess spatial variability and source influences. LURs were successfully developed to estimate pollutant concentrations throughout the study areas. Comparisons of development and predictive capabilities of LURs from these four cities are presented to address this issue of uniform application of LURs across study areas. Traffic and other urban variables were important predictors in the LURs although city-specific influences (such as border crossings) were also important. In addition, transferability of variables or LURs from one city to another may be problematic due to intercity differences and data availability or comparability. Thus, developing common predictors in future LURs may be difficult. PMID:23226985

  15. Observations of ozone and nitrogen dioxide profiles in TROICA experiments

    NASA Astrophysics Data System (ADS)

    Postylyakov, O. V.; Elokhov, A. S.; Belikov, I. B.; Igaev, A. I.; Elansky, N. F.

    Several expeditions TROICA on atmosphere investigation over continental Russian has been carried out using mobile railway carriage-laboratory in zonal (between Moscow and Khabarovsk) and meridional (between Murmansk and Kislovodsk) directions. The first measurements of gas profiles aboard a carriage-laboratory were performed in the scientific expeditions TROICA-4 (April 1997) along way Moscow-Khabarovsk-Moscow. To determine the ozone and nitrogen dioxide profiles, the express Umkehr method and zenith sky twilight measurements were used, respectively. The UV and visible spectra was recorded with an MDR-23 spectrophotometer aboard the moving carriage-laboratory coupled just behind an electric locomotive of a passenger train. Data on the total content and vertical profiles of impurities are obtained. These data reflect mainly the large-scale impurity distribution influenced by planetary waves. Significant variations in the total content and vertical distribution of impurities in the cross-section of a deep low representing a part of a circumpolar vortex are analyzed. The results of measurements are compared with the data obtained by TOMS, GOME and ground-based stations. A new carriage-laboratory has been equipped by optical remote sensing system based on image spectrometer Oriel MS257. It is capable to measure UV and visual spectral radiance incoming from several directions to determine the slant columns of ozone, nitrogen dioxide and other small gases. Using observations at a few wavelengths and several solar zenith angles vertical distribution of gases is retrieved. The first expedition (TROICA-8) of a new carriage-laboratory with the new optical remote sensing system is scheduled for February-March 2004. Results of previous expeditions as well as the first results of TROICA-8 will be presented. Effectiveness of using a moving laboratory of such a kind for validation of network and space observational data is discussed.

  16. Response of radish to nitrogen dioxide, sulfur dioxide, and ozone, alone and in combination

    SciTech Connect

    Reinert, R.A.; Gray, T.N.

    1981-04-01

    Effects on radish (Raphanus sativus L.) cv. Cherry Belle of nitrogen dioxide (NO/sub 2/), sulfur dioxide (SO/sub 2/), and ozone (O/sub 3/) alone and in combination at 0.2 and 0.4 ppM of each pollutant were studied. There was no difference in foilage or root weight of radish between exposure durations of 3 to 6 hours, and no significant interaction of hours with air pollutant and concentration. Ozone reduced root dry weight more at 0.4 ppM than at 0.2 ppM. Sulfur dioxide depressed the root/shoot ratio at both 0.2 and 0.4 ppM; however, when NO/sub 2/ and SO/sub 2/ were both present there was synergistic depression of the root/shoot ratio at 0.4 ppM. The average O/sub 3/-induced reduction in root weight of radish (1.75 g fresh and 101 mg dry, per plant) was additive in the presence of NO/sub 2/ and SO/sub 2/. The weight of the root was reduced even though the foilage was the direct receptor of the pollutant stress.

  17. 40 CFR Appendix S to Part 50 - Interpretation of the Primary National Ambient Air Quality Standards for Oxides of Nitrogen...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Ambient Air Quality Standards for Oxides of Nitrogen (Nitrogen Dioxide) S Appendix S to Part 50 Protection... National Ambient Air Quality Standards for Oxides of Nitrogen (Nitrogen Dioxide) 1. General (a) This... national ambient air quality standards for oxides of nitrogen as measured by nitrogen dioxide (“NO2...

  18. 40 CFR Appendix S to Part 50 - Interpretation of the Primary National Ambient Air Quality Standards for Oxides of Nitrogen...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... Ambient Air Quality Standards for Oxides of Nitrogen (Nitrogen Dioxide) S Appendix S to Part 50 Protection... National Ambient Air Quality Standards for Oxides of Nitrogen (Nitrogen Dioxide) 1. General (a) This... national ambient air quality standards for oxides of nitrogen as measured by nitrogen dioxide (“NO2...

  19. 40 CFR Appendix S to Part 50 - Interpretation of the Primary National Ambient Air Quality Standards for Oxides of Nitrogen...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... Ambient Air Quality Standards for Oxides of Nitrogen (Nitrogen Dioxide) S Appendix S to Part 50 Protection... National Ambient Air Quality Standards for Oxides of Nitrogen (Nitrogen Dioxide) 1. General (a) This... national ambient air quality standards for oxides of nitrogen as measured by nitrogen dioxide (“NO2...

  20. 40 CFR Appendix S to Part 50 - Interpretation of the Primary National Ambient Air Quality Standards for Oxides of Nitrogen...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Ambient Air Quality Standards for Oxides of Nitrogen (Nitrogen Dioxide) S Appendix S to Part 50 Protection... National Ambient Air Quality Standards for Oxides of Nitrogen (Nitrogen Dioxide) 1. General (a) This... national ambient air quality standards for oxides of nitrogen as measured by nitrogen dioxide (“NO2...

  1. Nitrogen Dioxide long term trends at mid and high latitudes by means of ground based observations

    NASA Astrophysics Data System (ADS)

    Bortoli, D.; Petritoli, A.; Giovanelli, G.; Kostadinov, I.; Ravegnani, F.

    2003-04-01

    The interactions between mid- and high latitudes atmospheric changes are going to be one of the main issue for the future of stratospheric and tropospheric chemistry research. A more detailed study of the ozone trends as well as a wider comprehension of the interactions with lower and higher latitudes are maybe the main arguments to which scientist should address their works in order to build-up a more detailed picture of what scenarios we have to face in the near future. GASCODs type spectrometers (Gas Analyzer Spectrometer Correlating Optical Differences) are installed at the "Ottavio Vittori" research station (44.11N, 10.42E, 2165 m asl) since June 1993, at the Italian Antarctic Station (74.69S, 164.12E) since December 1995 and at the STIL-BAS station (42.42N, 25.63E) since 1999. The instruments measure zenith scattered solar radiation between 407 and 464 nm. Nitrogen dioxide total column is retrieved with DOAS methodology. The seasonal trend of NO2 vc values is reported and it shows the expected behaviour: maximum values during the summer period while the minimum occur in the winter season in both the hemispheres. A typical behaviour of the AMPM ratio at high latitudes is highlight. A Fourier analysis is proposed as a tool to investigate the long-term components of nitrogen dioxide stratospheric amount. Results are presented and the NO2 trend is evidenced and commented. ACKNOWLEDGMENTS: The author Daniele Bortoli was financially supported by the Subprograma Ciência e Tecnologia do 3° Quadro Comunitário de Apoio. The National Antarctic Research Program (PNRA) and the Quantification and Interpretation of Long-Term UV-Vis Observations of the Stratosphere (QUILT) project supported this research.

  2. Nitrogen Dioxide Sterilization in Low-Resource Environments: A Feasibility Study

    PubMed Central

    Avasthi, Trisha; Trilling, Ariel

    2015-01-01

    Access to sterilization is a critical need for global healthcare, as it is one of the prerequisites for safe surgical care. Lack of sterilization capability has driven up healthcare infection rates as well as limited access to healthcare, especially in low-resource environments. Sterilization technology has for the most part been static and none of the established sterilization methods has been so far successfully adapted for use in low-resource environments on a large scale. It is evident that healthcare facilities in low-resource settings require reliable, deployable, durable, affordable, easily operable sterilization equipment that can operate independently of scarce resources. Recently commercialized nitrogen dioxide (NO2) sterilization technology was analyzed and adapted into a form factor suitable for use in low-resource environments. Lab testing was conducted in microbiological testing facilities simulating low-resource environments and in accordance with the requirements of the international sterilization standard ANSI/AAMI/ISO 14937 to assess effectiveness of the device and process. The feasibility of a portable sterilizer based on nitrogen dioxide has been demonstrated, showing that sterilization of medical instruments can occur in a form factor suitable for use in low-resource environments. If developed and deployed, NO2 sterilization technology will have the twin benefits of reducing healthcare acquired infections and limiting a major constraint for access to surgical care on a global scale. Additional benefits are achieved in reducing costs and biohazard waste generated by current health care initiatives that rely primarily on disposable kits, increasing the effectiveness and outreach of these initiatives. PMID:26098905

  3. Revising the slant column density retrieval of nitrogen dioxide observed by the Ozone Monitoring Instrument

    NASA Astrophysics Data System (ADS)

    Marchenko, S.; Krotkov, N. A.; Lamsal, L. N.; Celarier, E. A.; Swartz, W. H.; Bucsela, E. J.

    2015-06-01

    Nitrogen dioxide retrievals from the Aura/Ozone Monitoring Instrument (OMI) have been used extensively over the past decade, particularly in the study of tropospheric air quality. Recent comparisons of OMI NO2 with independent data sets and models suggested that the OMI values of slant column density (SCD) and stratospheric vertical column density (VCD) in both the NASA OMNO2 and Royal Netherlands Meteorological Institute DOMINO products are too large, by around 10-40%. We describe a substantially revised spectral fitting algorithm, optimized for the OMI visible light spectrometer channel. The most important changes comprise a flexible adjustment of the instrumental wavelength shifts combined with iterative removal of the ring spectral features; the multistep removal of instrumental noise; iterative, sequential estimates of SCDs of the trace gases in the 402-465 nm range. These changes reduce OMI SCD(NO2) by 10-35%, bringing them much closer to SCDs retrieved from independent measurements and models. The revised SCDs, submitted to the stratosphere-troposphere separation algorithm, give tropospheric VCDs ˜10-15% smaller in polluted regions, and up to ˜30% smaller in unpolluted areas. Although the revised algorithm has been optimized specifically for the OMI NO2 retrieval, our approach could be more broadly applicable.

  4. Effect of nitrogen dioxide, ozone, and peroxyacetyl nitrate on metabolic and pulmonary function

    SciTech Connect

    Drechsler-Parks, D.M. )

    1987-04-01

    The metabolic and pulmonary function responses were investigated in 32 non-smoking men and women (8 men and 8 women 18-26 years of age, and 8 men and 8 women 51-76 years of age) who were exposed for 2 hours to each of 8 conditions: (1) filtered air (FA), (2) 0.13 ppm peroxyacetyl nitrate (PAN), (3) 0.45 ppm ozone (O3), (4) 0.60 ppm nitrogen dioxide (NO2), (5) 0.13 ppm PAN + 0.45 ppm O3 (PAN/O3), (6) 0.13 ppm PAN + 0.60 ppm NO2 (PAN/NO2), (7) 0.60 ppm NO2 + 0.45 ppm O3 (NO2/O3), and (8) 0.13 ppm PAN + 0.60 ppm NO2 + 0.45 ppm O3 (PAN/NO2/O3). The subjects alternated 20-min periods of rest (n = 3) and cycle ergometer exercise (n = 3) at a work load predetermined to elicit a ventilatory minute volume (VE) of approximately 25 L/min (BTPS). Functional residual capacity (FRC) was determined pre- and post-exposure. Forced vital capacity (FVC) was determined before and after exposure, and 5 min after each exercise period. Heart rate was monitored throughout each exposure, and VE was measured during the last 2 min of each exercise period. Exposure to FA, PAN, NO2, and PAN/NO2 had no effect on any measure of pulmonary or metabolic function. Ozone was primarily responsible for the pulmonary function effects observed. There was no significant difference between the responses to O3 exposure and the responses to the three O3 mixtures, indicating no interactions between the pollutants. The results suggest that women may be somewhat more responsive to O3 exposure than men, and that older people (51-76 years of age) may be less responsive to O3 than younger people (18-26 years of age).

  5. Rapid growth in nitrogen dioxide pollution over Western China, 2005-2013

    NASA Astrophysics Data System (ADS)

    Cui, Yuanzheng; Lin, Jintai; Song, Chunqiao; Liu, Mengyao; Yan, Yingying; Xu, Yuan; Huang, Bo

    2016-05-01

    Western China has experienced rapid industrialization and urbanization since the implementation of the National Western Development Strategies (the "Go West" movement) in 1999. This transition has affected the spatial and temporal characteristics of nitrogen dioxide (NO2) pollution. In this study, we analyze the trends and variability of tropospheric NO2 vertical column densities (VCDs) from 2005 to 2013 over Western China, based on a wavelet analysis on monthly mean NO2 data derived from the Ozone Monitoring Instrument (OMI) measurements. We focus on the anthropogenic NO2 by subtracting region-specific "background" values dominated by natural sources. After removing the background influences, we find significant anthropogenic NO2 growth over Western China between 2005 and 2013 (8.6 ± 0.9 % yr-1 on average, relative to 2005), with the largest increments (15 % yr-1 or more) over parts of several city clusters. The NO2 pollution in most provincial-level regions rose rapidly from 2005 to 2011 but stabilized or declined afterwards. The NO2 trends were driven mainly by changes in anthropogenic emissions, as confirmed by a nested GEOS-Chem model simulation and a comparison with Chinese official emission statistics. The rate of NO2 growth during 2005-2013 reaches 11.3 ± 1.0 % yr-1 over Northwestern China, exceeding the rates over Southwestern China (5.9 ± 0.6 % yr-1) and the three well-known polluted regions in the east (5.3 ± 0.8 % yr-1 over Beijing-Tianjin-Hebei, 4.0 ± 0.6 % yr-1 over the Yangtze River Delta, and -3.3 ± 0.3 % yr-1 over the Pearl River Delta). Subsequent socioeconomic analyses suggest that the rapid NO2 growth over Northwestern China is likely related to the fast developing resource- and pollution-intensive industries along with the "Go West" movement as well as relatively weak emission controls. Further efforts should be made to alleviate NOx pollution to achieve sustainable development in Western China.

  6. Rapid growth in nitrogen dioxide pollution over Western China, 2005-2013

    NASA Astrophysics Data System (ADS)

    Cui, Y.-Z.; Lin, J.-T.; Song, C.; Liu, M.-Y.; Yan, Y.-Y.; Xu, Y.; Huang, B.

    2015-12-01

    Western China has experienced rapid industrialization and urbanization since the implementation of the National Western Development Strategies (the "Go West" movement) in 1999. This transition has affected the spatial and temporal characteristics of nitrogen dioxide (NO2) pollution. In this study, we analyze the trends and variability of tropospheric NO2 vertical column densities (VCDs) from 2005 to 2013 over Western China, based on a wavelet analysis on monthly mean NO2 data derived from the Ozone Monitoring Instrument (OMI) measurements. We focus on the anthropogenic NO2 by subtracting region-specific "background" values dominated by natural sources. We find significant NO2 growth over Western China between 2005 and 2013 (8.6 ± 0.9 % yr-1 on average, relative to 2005), with the largest increments (15 % yr-1 or more) over parts of several city clusters. The NO2 pollution in most provincial regions rose rapidly from 2005 to 2011 but stabilized or declined afterwards. The NO2 trends were driven mainly by changes in anthropogenic emissions, as confirmed by a nested GEOS-Chem model simulation and a comparison with Chinese official emission statistics. The rate of NO2 growth during 2005-2013 reaches 11.3 ± 1.0 % yr-1 over Northwestern China, exceeding the rates over Southwestern China (5.9 ± 0.6 % yr-1) and the three well-known polluted regions in the east (5.3 ± 0.8 % yr-1 over Beijing-Tianjin-Hebei, 4.0 ± 0.6 % yr-1} over the Yangtze River Delta, and -3.3 ± 0.3 % yr-1 over the Pearl River Delta). Additional socioeconomic analyses suggest that the rapid NO2 growth in Northwestern China is likely related to the fast developing resource- and pollution-intensive industries along with the "Go West" movement as well as relatively weak emission controls. Further efforts should be made to alleviate NOx pollution to achieve sustainable development in Western China.

  7. Fine particulate air pollution, nitrogen dioxide, and systemic autoimmune rheumatic disease in Calgary, Alberta

    PubMed Central

    Bernatsky, Sasha; Smargiassi, Audrey; Johnson, Markey; Kaplan, Gilaad G.; Barnabe, Cheryl; Svenson, Larry; Brand, Allan; Bertazzon, Stefania; Hudson, Marie; Clarke, Ann E; Fortin, Paul; Edworthy, Steven; Bélisle, Patrick; Joseph, Lawrence

    2015-01-01

    Objective To estimate the association between fine particulate (PM2.5) and nitrogen dioxide (NO2) pollution and systemic autoimmune rheumatic diseases (SARDs). Methods Associations between ambient air pollution (PM2.5 and NO2) and SARDs were assessed using land-use regression models for Calgary, Alberta and administrative health data (1993-2007). SARD case definitions were based on ≥2 physician claims, or ≥1 rheumatology billing code; or ≥1 hospitalization code (for systemic lupus, Sjogren's Syndrome, scleroderma, polymyositis, dermatomyositis, or undifferentiated connective tissue disease). Bayesian hierarchical latent class regression models estimated the probability that each resident was a SARD case, based on these case definitions. The sum of individual level probabilities provided the estimated number of cases in each area. The latent class model included terms for age, sex, and an interaction term between age and sex. Bayesian logistic regression models were used to generate adjusted odds ratios (OR) for NO2 and PM2.5. pollutant models, adjusting for neighborhood income, age, sex, and an interaction between age and sex. We also examined models stratified for First-Nations (FN) and non-FN subgroups. Results Residents that were female and/or aged > 45 had a greater probability of being a SARD case, with the highest OR estimates for older females. Independently, the odds of being a SARDs case increased with PM2.5 levels, but the results were inconclusive for NO2. The results stratified by FN and Non-FN groups were not distinctly different. Conclusion In this urban Canadian sample, adjusting for demographics, exposure to PM2.5 was associated with an increased risk of SARDs. The results for NO2 were inconclusive. PMID:25988990

  8. Ambient fine particulate matter, nitrogen dioxide, and hypertensive disorders of pregnancy in New York City

    PubMed Central

    Savitz, David A.; Elston, Beth; Bobb, Jennifer F.; Clougherty, Jane E.; Dominici, Francesca; Ito, Kazuhiko; Johnson, Sarah; McAlexander, Tara; Ross, Zev; Shmool, Jessie L.C.; Matte, Thomas D.; Wellenius, Gregory A.

    2016-01-01

    BACKGROUND Previous studies suggested a possible association between fine particulate matter air pollution (PM2.5) and nitrogen dioxide (NO2) and the development of hypertensive disorders of pregnancy, but effect sizes have been small and methodologic weaknesses preclude firm conclusions. METHODS We linked birth certificates in New York City in 2008-2010 to hospital discharge diagnoses and estimated air pollution exposure based on maternal address. The New York City Community Air Survey provided refined estimates of PM2.5 and NO2 at the maternal residence. We estimated the association between exposures to PM2.5 and NO2 in the first and second trimester and risk of gestational hypertension, mild preeclampsia, and severe preeclampsia among 268,601 births. RESULTS In unadjusted analyses, we found evidence of a positive association between both pollutants and gestational hypertension. However, after adjustment for individual covariates, socioeconomic deprivation, and delivery hospital, we did not find evidence of an association between PM2.5 or NO2 in the first or second trimester and any of the outcomes. CONCLUSIONS Our data did not provide clear evidence of an effect of ambient air pollution on hypertensive disorders of pregnancy. Results need to be interpreted with caution considering the quality of the available exposure and health outcome measures and the uncertain impact of adjusting for hospital. Relative to previous studies, which have tended to identify positive associations with PM2.5 and NO2, our large study size, refined air pollution exposure estimates, hospital-based disease ascertainment, and little risk of confounding by socioeconomic deprivation, does not provide evidence for an association. PMID:26237745

  9. Uricase Inhibits Nitrogen Dioxide-Promoted Allergic Sensitization to Inhaled Ovalbumin Independent of Uric Acid Catabolism.

    PubMed

    Ather, Jennifer L; Burgess, Edward J; Hoyt, Laura R; Randall, Matthew J; Mandal, Mridul K; Matthews, Dwight E; Boyson, Jonathan E; Poynter, Matthew E

    2016-09-01

    Nitrogen dioxide (NO2) is an environmental air pollutant and endogenously generated oxidant that contributes to the exacerbation of respiratory disease and can function as an adjuvant to allergically sensitize to an innocuous inhaled Ag. Because uric acid has been implicated as a mediator of adjuvant activity, we sought to determine whether uric acid was elevated and participated in a mouse model of NO2-promoted allergic sensitization. We found that uric acid was increased in the airways of mice exposed to NO2 and that administration of uricase inhibited the development of OVA-driven allergic airway disease subsequent to OVA challenge, as well as the generation of OVA-specific Abs. However, uricase was itself immunogenic, inducing a uricase-specific adaptive immune response that occurred even when the enzymatic activity of uricase had been inactivated. Inhibition of the OVA-specific response was not due to the capacity of uricase to inhibit the early steps of OVA uptake or processing and presentation by dendritic cells, but occurred at a later step that blocked OVA-specific CD4(+) T cell proliferation and cytokine production. Although blocking uric acid formation by allopurinol did not affect outcomes, administration of ultra-clean human serum albumin at protein concentrations equivalent to that of uricase inhibited NO2-promoted allergic airway disease. These results indicate that, although uric acid levels are elevated in the airways of NO2-exposed mice, the powerful inhibitory effect of uricase administration on allergic sensitization is mediated more through Ag-specific immune deviation than via suppression of allergic sensitization, a mechanism to be considered in the interpretation of results from other experimental systems. PMID:27465529

  10. Nitrogen dioxide induced changes in level of free fatty acids, triglyceride, esterified fatty acid, ganglioside and lipase activity in the guinea pig brain

    SciTech Connect

    Farahani, H.; Hasan, M. )

    1992-02-01

    The biochemical response to controlled inhalation of nitrogen dioxide (NO2) was studied in 18 male guinea pigs. Animals were exposed to 2.5, 5.0, and 10 ppm NO2 for 2h daily for 35 consecutive days, and the results compared with six control animals exposed to filtered air for 2h daily for same period. Five biochemical parameters, including triglyceride, free fatty acids, esterified fatty acid, ganglioside and lipase activity were measured immediately after the last day of exposure. At 2.5 ppm NO2 inhalation no significant changes occurred in any region of the central nervous system (CNS). While as the dose concentration was increased to 5 and 10 ppm nitrogen dioxide, significant dose-related alteration were observed in the levels of triglyceride, free fatty acid, esterified fatty acid, ganglioside and lipase activity in the different regions of the guinea pig CNS.

  11. Association of indoor nitrogen dioxide with respiratory symptoms and pulmonary function in children

    SciTech Connect

    Neas, L.M.; Dockery, D.W.; Ware, J.H.; Spengler, J.D.; Speizer, F.E.; Ferris, B.G. Jr. )

    1991-07-15

    The effect of indoor nitrogen dioxide on the cumulative incidence of respiratory symptoms and pulmonary function level was studied in a cohort of 1,567 white children aged 7-11 years examined in six US cities from 1983 through 1988. Week-long measurements of nitrogen dioxide were obtained at three indoor locations over 2 consecutive weeks in both the winter and the summer months. The household annual average nitrogen dioxide concentration was modeled as a continuous variable and as four ordered categories. Multiple logistic regression analysis of symptom reports from a questionnaire administered after indoor monitoring showed that a 15-ppb increase in the household annual nitrogen dioxide mean was associated with an increased cumulative incidence of lower respiratory symptoms (odds ratio (OR) = 1.4, 95% confidence interval (95% Cl) 1.1-1.7). The response variable indicated the report of one or more of the following symptoms: attacks of shortness of breath with wheeze, chronic wheeze, chronic cough, chronic phlegm, or bronchitis. Girls showed a stronger association (OR = 1.7, 95% Cl 1.3-2.2) than did boys (OR = 1.2, 95% Cl 0.9-1.5). An analysis of pulmonary function measurements showed no consistent effect of nitrogen dioxide. These results are consistent with earlier reports based on categorical indicators of household nitrogen dioxide sources and provide a more specific association with nitrogen dioxide as measured in children's homes.

  12. Ambient Fine Particulate Matter, Nitrogen Dioxide, and Preterm Birth in New York City

    PubMed Central

    Johnson, Sarah; Bobb, Jennifer F.; Ito, Kazuhiko; Savitz, David A.; Elston, Beth; Shmool, Jessie L.C.; Dominici, Francesca; Ross, Zev; Clougherty, Jane E.; Matte, Thomas

    2016-01-01

    Background: Recent studies have suggested associations between air pollution and various birth outcomes, but the evidence for preterm birth is mixed. Objective: We aimed to assess the relationship between air pollution and preterm birth using 2008–2010 New York City (NYC) birth certificates linked to hospital records. Methods: We analyzed 258,294 singleton births with 22–42 completed weeks gestation to nonsmoking mothers. Exposures to ambient fine particles (PM2.5) and nitrogen dioxide (NO2) during the first, second, and cumulative third trimesters within 300 m of maternal address were estimated using data from the NYC Community Air Survey and regulatory monitors. We estimated the odds ratio (OR) of spontaneous preterm (gestation < 37 weeks) births for the first- and second-trimester exposures in a logistic mixed model, and the third-trimester cumulative exposures in a discrete time survival model, adjusting for maternal characteristics and delivery hospital. Spatial and temporal components of estimated exposures were also separately analyzed. Results: PM2.5 was not significantly associated with spontaneous preterm birth. NO2 in the second trimester was negatively associated with spontaneous preterm birth in the adjusted model (OR = 0.90; 95% CI: 0.83, 0.97 per 20 ppb). Neither pollutant was significantly associated with spontaneous preterm birth based on adjusted models of temporal exposures, whereas the spatial exposures showed significantly reduced odds ratios (OR = 0.80; 95% CI: 0.67, 0.96 per 10 μg/m3 PM2.5 and 0.88; 95% CI: 0.79, 0.98 per 20 ppb NO2). Without adjustment for hospital, these negative associations were stronger. Conclusion: Neither PM2.5 nor NO2 was positively associated with spontaneous preterm delivery in NYC. Delivery hospital was an important spatial confounder. Citation: Johnson S, Bobb JF, Ito K, Savitz DA, Elston B, Shmool JL, Dominici F, Ross Z, Clougherty JE, Matte T. 2016. Ambient fine particulate matter, nitrogen dioxide, and

  13. Atmospheric nitrogen oxides (NO and NO2) at Dome C: first observations and implications for reactive nitrogen cycling above the East Antarctic Ice Sheet

    NASA Astrophysics Data System (ADS)

    Frey, M. M.; Brough, N.; France, J. L.; King, M. D.; Erbland, J.; Savarino, J.; Anderson, P. S.; Jones, A. E.; Wolff, E. W.

    2010-05-01

    The nitrogen oxides NO and NO2 (NOx) play a key role in determining the oxidizing capacity of the boundary layer in high latitudes. This influence is achieved via the photolysis of NO2 - the only source for in situ production of tropospheric ozone (O3) - and through shifting HOx radical partitioning towards the hydroxyl radical (OH) via the reaction NO + HO2 - OH + NO2. Previous field campaigns in the Arctic and Antarctic have demonstrated that the polar snow pack can release significant emissions of NOx and that one of the major driving mechanisms is UV-photolysis of snow nitrate (NO3-). Unusually high levels of NO observed at South Pole and on an airborne campaign suggested that the East Antarctic Ice Sheet (EAIS) can be perceived as a gigantic chemical reactor, processing many chemical trace species at the surface and thereby modifying their concentration eventually preserved in ice cores. However, the database for a quantitative understanding of reactive nitrogen recycling across Antarctica is still weak. Here, we present first measurements of atmospheric NOx mixing ratios and fluxes at Dome C (DC), East Antarctica (75.1°S 123.3°E, 3233 m) during austral summer 2009/2010. As seen previously, NO mixing ratios were highly perturbed, ranging between 10 pptv and >600 pptv, but unlike at South Pole showed a strong diurnal variability. Concentration maxima occurring in the evening hours coincided with the strongest gradients between the snow surface and 4.0 m, highlighting the importance of the interplay between snow pack source strength and the evolution of boundary layer depth. Conversely, surface-near firn air levels of NOx varied in phase with solar radiation, consistent with a photolytic source in the surface-near snow. Observed NOx emissions were compared to calculations based on NO3- concentration profiles and e-folding depths of actinic flux measured in the upper snowpack. Contrary to South Pole, surface observations at DC are thought to be more

  14. Atmospheric nitrogen oxides (NO and NO2) in ambient and firn interstitial air at Dome C: implications for modeling reactive nitrogen cycling on the East Antarctic Plateau

    NASA Astrophysics Data System (ADS)

    Frey, M. M.; Brough, N.; Thomas, J. L.; Jones, A. E.; Savarino, J.

    2012-04-01

    The nitrogen oxides NO and NO2 (NOx) play a key role in determining the oxidizing capacity of the boundary layer in high latitudes. This influence is achieved via the photolysis of NO2 - the only source for in situ production of tropospheric ozone (O3) - and through shifting HOx radical partitioning towards the hydroxyl radical (OH) via the reaction NO + HO2 → OH + NO2. Numerous field campaigns in the high latitudes demonstrated that the polar snow pack can emit significant amounts of NOx and that one of the major driving mechanisms is UV-photolysis of nitrate (NO3-) in snow. Previously, we presented the first measurements of atmospheric NOx at Dome C, East Antarctica (75.1°S 123.3°E, 3233 m) during austral summer 2009/2010. NOx mixing ratios were highly perturbed, with a mean of 240 pptv (range 10-1000 pptv), but unlike at South Pole showed a strong diurnal variability. The timing of daily concentration extrema, the minimum at noon and the maximum in the evening, was shown to be largely determined by the dynamics of the local boundary layer. Here we focus on NOx observations in the firn interstitial air: gas phase mixing ratios at 10 cm depth were up to 10-fold those in the air above the snow and varied in phase with solar radiation, consistent with a photolytic source in the surface-near snow. Furthermore, shading experiments and firn air profiles suggest the existence of a NOx reservoir in the upper snow pack. And finally, we estimate the total oxidant burden in the open pore space, a quantity, which is not easily measured, using NOx flux measurements and deviations of the NO2:NO ratio from steady state. Observations were compared to the 1-D atmosphere-snow model MISTRA-SNOW, used previously to investigate NOx snow-photochemistry at Summit/Greenland. Model runs constrained by wind speed, snow pack profiles of NO3- concentrations and actinic flux are in close agreement with observations in ambient air. We examine how the parameterization of reactive nitrogen

  15. Spatial variance and assessment of nitrogen dioxide pollution in major cities of Pakistan along N5-Highway.

    PubMed

    Shabbir, Yasir; Khokhar, Muhammad Fahim; Shaiganfar, Reza; Wagner, Thomas

    2016-05-01

    This paper discusses the findings of the first car MAX-DOAS (multi-axis differential optical absorption spectroscopy) field campaign (300km long) along the National Highway-05 (N5-Highway) of Pakistan conducted on 13 and 14 November, 2012. The main objective of the field campaign was to assess the spatial distribution of tropospheric nitrogen dioxide (NO2) columns and corresponding concentrations along the N5-Highway from Islamabad to Lahore. Source identification of NO2 revealed that the concentrations were higher within major cities along the highway. The highest NO2 vertical column densities (NO2 VCDs) were found around two major cities of Rawalpindi and Lahore. This study also presents a comparison of NO2 VCDs measured by the ozone monitoring instrument (OMI) and car MAX-DOAS observations. The comparison revealed similar spatial distribution of the NO2 columns with both car MAX-DOAS and satellite observations, but the car MAX-DOAS observations show much more spatial details. Maximum NO2 VCD retrieved from car MAX-DOAS observations was up to an order of magnitude larger than the OMI observations in urban areas. PMID:27155404

  16. Effects of nitrogen dioxide and its acid mist on reactive oxygen species production and antioxidant enzyme activity in Arabidopsis plants.

    PubMed

    Liu, Xiaofang; Hou, Fen; Li, Guangke; Sang, Nan

    2015-08-01

    Nitrogen dioxide (NO2) is one of the most common and harmful air pollutants. To analyze the response of plants to NO2 stress, we investigated the morphological change, reactive oxygen species (ROS) production and antioxidant enzyme activity in Arabidopsis thaliana (Col-0) exposed to 1.7, 4, 8.5, and 18.8 mg/m(3) NO2. The results indicate that NO2 exposure affected plant growth and chlorophyll (Chl) content, and increased oxygen free radical (O2(-)) production rate in Arabidopsis shoots. Furthermore, NO2 elevated the levels of lipid peroxidation and protein oxidation, accompanied by the induction of antioxidant enzyme activities and change of ascorbate (AsA) and glutathione (GSH) contents. Following this, we mimicked nitric acid mist under experimental conditions, and confirmed the antioxidant mechanism of the plant to the stress. Our results imply that NO2 and its acid mist caused pollution risk to plant systems. During the process, increased ROS acted as a signal to induce a defense response, and antioxidant status played an important role in plant protection against NO2/nitric acid mist-caused oxidative damage. PMID:26257351

  17. Near-lifetime exposure of the rat to a simulated urban profile of nitrogen dioxide: pulmonary function evaluation.

    PubMed

    Tepper, J S; Costa, D L; Winsett, D W; Stevens, M A; Doerfler, D L; Watkinson, W P

    1993-01-01

    To investigate the potential for up to a near-lifetime exposure to high-ambient levels of nitrogen dioxide (NO2) to induce functional lung damage, groups of rats were exposed to air or a simulated urban profile of NO2 (0.5 ppm background, 1.5 ppm peak) for 1, 3, 13, 52, or 78 weeks. The dynamic, static, and diffusional characteristics of the lung were evaluated postexposure in anesthetized rats. Furthermore, for the 13-, 52-, and 78-week groups, additional animals were tested after a 6-, 26-, or 17-week period in filtered air, respectively. No significant NO2 differences between exposed and control animals were found for the nitrogen washout, compliance, lung volume, or diffusion capacity of carbon monoxide measurements. At 78 weeks, however, a reduction in delta FEF25%, an estimate of convexity in the later portion of the forced expiratory flow volume curve, was observed. Breathing patterns and mechanisms were also assessed postexposure in a parallel group of similarly exposed unanesthetized rats. These rats were examined during a filtered air, 4 and 8% carbon dioxide (CO2) challenge. In the unanesthetized rat, frequency of breathing was significantly decreased and tidal volume, expiratory resistance, and inspiratory and expiratory times tended to increase. For several of these variables, the largest response also occurred at 78 weeks and seemed to be exacerbated by CO2 challenge.(ABSTRACT TRUNCATED AT 250 WORDS) PMID:8432431

  18. Characterization of a spatial gradient of nitrogen dioxide across a United States-Mexico border city during winter.

    PubMed

    Gonzales, Melissa; Qualls, Clifford; Hudgens, Edward; Neas, Lucas

    2005-01-20

    A gradient of ambient nitrogen dioxide (NO(2)) concentration is demonstrated across metropolitan El Paso, Texas (USA), a city located on the international border between the United States and Mexico. Integrated measurements of NO(2) were collected over 7 days at 20 elementary schools and 4 air quality monitoring stations located throughout the city during typical winter atmospheric conditions. Replicate passive monitors were co-located with chemiluminescence analyzers at the monitoring stations for two consecutive 7-day periods. The passive measurements correlated with the analyzer measurements (R(2)=0.74) with precision of 2.5+/-2.2 ppb. Nitrogen dioxide concentrations ranged from 11.0 to 37.5 ppb (mean 20.6+/-7.1 ppb). In a multivariate regression model, the site elevation and distances to a main highway and to an international port of entry from Mexico explained 81% of the variance in the passive measurements. The results of this pilot study indicate that proximity to vehicle-related sources of NO(2) and site elevation are key predictors for future, more detailed assessments of vehicle-related air pollution exposure in the El Paso region. PMID:15626387

  19. Detection of atmospheric nitrogen dioxide using a miniaturised fibre-optic spectroscopy system and the ambient sunlight.

    PubMed

    Morales, J A; Walsh, J E

    2005-07-01

    A miniaturised fibre-optic spectrometer based system is presented for direct detection of one of the major atmospheric pollutants, nitrogen dioxide, by absorption spectroscopy using the ambient sunlight as light source. The detection system consists of a 10 cm collimator assembly, a fibre-optic cable and a portable diode-array spectrometer. The absorbance spectrum of the open-path is calculated using a reference spectrum recorded when the nitrogen dioxide (NO2) concentration in the atmosphere is low. The relative concentration of the pollutant is calculated normalising the detected spectra and subtracting the background broadband spectrum from the specific NO2 absorbance features, since the broadband spectrum changes according to atmospheric conditions and solar intensity. Wavelengths between 400 and 500 nm are used in order to maximise sensitivity and to avoid interference from other species. Calibration is carried out using Tedlar sample bags of known concentration of the pollutant. A commercial differential optical absorption spectroscopy (DOAS) system is used as a reference standard detection system to compare the results with the new system. Results show that detection of NO2 at typical urban atmospheric levels has been achieved using an inexpensive field based fibre-optic spectrometer and a readily available, easy to align, light source. In addition the new system can be used to get a semi-quantitative estimation of the nitrogen dioxide concentration within errors of 20%. While keeping the typical benefits of open-path techniques, the new system has important advantages over them such as cost, simplicity and portability. PMID:15911394

  20. Growth of radish and marigold following repeated exposure to nitrogen dioxide, sulfur dioxide, and ozone

    SciTech Connect

    Reinert, R.A.; Sanders, J.S.

    1982-02-01

    Radish and marigold plants were exposed to 0.3 ppm of nitrogen dioxide (NO/sub 2/), sulfur dioxide (SO/sub 2/), and/or ozone (O/sub 3/) nine times during a 3-wk period. No interactions among NO/sub 2/, SO/sub 2/, and O/sub 3/ were detected in measurement of radish foliage and root dry weight. Treatments containing O/sub 3/ reduced radish foliage and root (hypocotyl) dry weight 356 and 531 mg/plant, respectively. Interactions among NO/sub 2/, SO/sub 2/, and O/sub 3/ occurred in shoots and roots of marigold. SO/sub 2/ alone reduced marigold shoot and root dry weight, but this effect was reversed in the presence of O/sub 3/. The suppressive effect of SO/sub 2/ on root weight was also reversed by NO/sub 3/. Treatments containing SO/sub 2/ reduced dry flower weight 0.17 g/plant, but effects of the pollutant interactions observed in shoots and roots were not present.

  1. Growth of radish and marigold following repeated exposure to nitrogen dioxide, sulfur dioxide, and ozone

    SciTech Connect

    Reinert, R.A.; Sanders, J.S.

    1982-02-01

    Radish and marigold plants were exposed to 0.3 ppM of nitrogen dioxide (NO/sub 2/), sulfur dioxide (SO/sub 2/), and /or ozone (O/sub 3/) nine times during a 3-wk period. No interactions among NO/sub 2/, SO/sub 2/, and O/sub 3/ were detected in measurement of radish foliage and root dry weight. Treatments containing O/sub 3/ reduced radish foliage and root (hypocotyl) dry weight 356 and 531 mg/plant, respectively. Interactions among NO/sub 2/, SO/sub 2/ and O/sub 3/ occurred in shoots and roots of marigold. SO/sub 2/ alone reduced marigold shoot and root dry weight, but this effect was reversed in the presence of O/sub 3/. The suppressive effect of SO/sub 2/ on root weight was also reversed by NO/sub 2/. Treatments containing SO/sub 2/ reduced dry flower weight 0.17 g/plant, but effects of the pollutant interactions observed in shoots and roots were not present. 8 references, 2 tables.

  2. NATIONAL PERFORMANCE AUDIT PROGRAM: 1979 PROFICIENCY SURVEYS FOR SULFUR DIOXIDE, NITROGEN DIOXIDE, CARBON MONOXIDE, SULFATE, NITRATE, LEAD AND HIGH VOLUME FLOW

    EPA Science Inventory

    The Quality Assurance Division of the Environmental Monitoring Systems Laboratory, Research Triangle Park, North Carolina, administers semiannual Surveys of Analytical Proficiency for sulfur dioxide, nitrogen dioxide, carbon monoxide, sulfate, nitrate and lead. Sample material, s...

  3. Nitrogen Dioxide and Allergic Sensitization in the 2005–2006 National Health and Nutrition Examination Survey

    PubMed Central

    Weir, Charles H.; Yeatts, Karin B.; Sarnat, Jeremy A.; Vizuete, William; Salo, Päivi M.; Jaramillo, Renee; Cohn, Richard D.; Chu, Haitao; Zeldin, Darryl C.; London, Stephanie J.

    2014-01-01

    Background Allergic sensitization is a risk factor for asthma and allergic diseases. The relationship between ambient air pollution and allergic sensitization is unclear. Objective To investigate the relationship between ambient air pollution and allergic sensitization in a nationally representative sample of the US population. Methods We linked annual average concentrations of nitrogen dioxide (NO2), particulate matter ≤ 10 µm (PM10), particulate matter ≤ 2.5 µm (PM25), and summer concentrations of ozone (O3), to allergen-specific immunoglobulin E (IgE) data for participants in the 2005–2006 National Health and Nutrition Examination Survey (NHANES). In addition to the monitor-based air pollution estimates, we used the Community Multiscale Air Quality (CMAQ) model to increase the representation of rural participants in our sample. Logistic regression with population-based sampling weights was used to calculate adjusted prevalence odds ratios per 10 ppb increase in O3 and NO2, per 10 µg/m3 increase in PM10, and per 5 µg/m3 increase in PM2.5 adjusting for race, gender, age, socioeconomic status, smoking, and urban/rural status. Results Using CMAQ data, increased levels of NO2 were associated with positive IgE to any (OR 1.15, 95% CI 1.04, 1.27), inhalant (OR 1.17, 95% CI 1.02, 1.33), and outdoor (OR 1.16, 95% CI 1.03, 1.31) allergens. Higher PM2.5 levels were associated with positivity to indoor allergen-specific IgE (OR 1.24, 95% CI 1.13, 1.36). Effect estimates were similar using monitored data. Conclusions Increased ambient NO2 was consistently associated with increased prevalence of allergic sensitization. PMID:24045117

  4. Indoor nitrogen dioxide in five Chattangooga, Tennessee public housing developments

    SciTech Connect

    Parkhurst, W.J.; Harper, J.P. ); Spengler, J.D.; Fraumeni, L.P.; Majahad, A.M. ); Cropp, J.W. )

    1988-01-01

    This report summarizes an indoor nitrogen dioxide (NO{sub 2}) sampling study conducted during January through March of 1987 in five Chattanooga public housing developments. The origins of this study date to the summer of 1983 when the Piney Woods Community Organization (a citizens action group) expressed concern about toxic industrial air pollution and the effects it might have on their community. In response to these concerns, the Chattanooga-Hamilton County Air Pollution Control Bureau (Bureau) requested assistance from the Tennessee Department of Health and Environment (TDHE) in conducting a community health survey and assistance from the Tennessee Valley Authority (TVA) in conducting a community air quality measurement program. The TDHE community health study did not find any significant differences between the mortality statistics for the Piney Woods community and a demographically similar control group. However, a health survey revealed that Piney Woods residents did not have a statistically significant higher self-reported prevalence of cough, wheezing, phlegm, breathlessness, colds, and respiratory illness.

  5. Mechanisms of Nitrogen Dioxide Reactions: Initiation of Lipid Peroxidation and the Production of Nitrous Acid

    NASA Astrophysics Data System (ADS)

    Pryor, William A.; Lightsey, John W.

    1981-10-01

    The reactions of nitrogen dioxide with cyclohexene have been studied as a model for the reactions that occur between nitrogen dioxide in smoggy air and unsaturated fatty acids in pulmonary lipids. As predicted from earlier studies at high nitrogen dioxide concentrations, this gas reacts with cyclohexene predominantly by addition to the double bond at nitrogen dioxide concentrations of I percent (10,000 parts per million) to 40 percent in nitrogen; in the presence of air or oxygen, this reaction initiates the autoxidation of the alkene. However, at concentrations below 100 parts per million in nitrogen, nitrogen dioxide reacts with cyclohexene almost exclusively by abstraction of allylic hydrogen; this unexpected reaction also initiates the autoxidation of the alkene in the presence of oxygen or air, but it leads to the production of nitrous acid rather than of a product containing a nitro group attached to a carbon atom. The nitrous acid can react with amines to produce nitrosamines. Moreover, the nitrite ion produced by the hydrogen abstraction mechanism would be expected to diffuse throughout the body, unlike nitrated lipids that would be confined to the pulmonary cavity. These findings have been confirmed with methyl oleate, linoleate, and linolenate; some of the kinetic features of the nitrogen dioxideinitiated autoxidation of these unsaturated fatty acids have been studied.

  6. Ozone and nitrogen dioxide ground based monitoring by zenith sky visible spectrometry in Arctic and Antarctic

    NASA Technical Reports Server (NTRS)

    Pommereau, J. P.; Goutail, F.

    1988-01-01

    Unattended diode array spectrometers have been designed for ground based stratospheric trace species monitoring by zenith sky visible spectrometry. Measurements are performed with a 1.0 nm resolution between 290 nm and 590 nm in order to allow simultaneous evaluations of column densities of ozone, nitrogen dioxide. Field tests have shown that the species can be monitored with a precision of + or - 2 Dobson for the first and + or - 2.10 to the 15th mol/sq cm for the second, although the absolute accuracy of the method is limited by the error of the estimation of the atmospheric optical path of the scattered light. Two identical instruments were set up in January 1988, one in Antarctica at Dumont d'Urville (66 S, 140 E) to be operated all year and another one in the Arctic at ESRANGE at Kiruna (68 N; 22 E) which will operate to the final warming of spring 1988. The data are processed in real time at both stations. O3 and NO2 columns are transmitted together with surface and stratospheric temperature and winds. They are also recorded for further treatment and search for OClO and BrO. Only one month of data from Antarctica is available at the moment. Obtained during polar summer, they cannot show more than stable columns of O3 and NO2 and for the last species, the buildup of its diurnal variation.

  7. The reaction of hydrogen peroxide with nitrogen dioxide and nitric oxide.

    NASA Technical Reports Server (NTRS)

    Gray, D.; Lissi, E.; Heicklen, J.

    1972-01-01

    The reactions were studied with the aid of a mass spectrometer. A pinhole bleed system provided continuous sampling of the gas mixture in the cell during the reaction. It was found that the homogeneous reactions of nitric oxide and nitrogen dioxide with hydrogen peroxide are too slow to be of any significance in the upper atmosphere. However, the heterogeneous reactions may be important in the conversion of nitric oxide to nitrogen dioxide in the case of polluted urban atmospheres.

  8. Infrared spectrum of the complex of formaldehyde with carbon dioxide in argon and nitrogen matrices

    NASA Technical Reports Server (NTRS)

    Van Der Zwet, G. P.; Allamandola, Louis J.; Baas, F.; Greenberg, J. M.

    1989-01-01

    The complex of formaldehyde with carbon dioxide has been studied by infrared spectroscopy in argon and nitrogen matrices. The shifts relative to the free species show that the complex is weak and similar in argon and nitrogen. The results give evidence for T-shaped complexes, which are isolated in several configurations. Some evidence is also presented which indicates that, in addition to the two well-known sites in argon, carbon dioxide can be trapped in a third site.

  9. Evaluation of nitrogen dioxide photolysis rates in an urban area using data from the 1997 Southern California Ozone Study

    NASA Astrophysics Data System (ADS)

    Vuilleumier, Laurent; Bamer, Jeffrey T.; Harley, Robert A.; Brown, Nancy J.

    The photolysis of nitrogen dioxide and formaldehyde are two of the most influential reactions in the formation of photochemical air pollution, and their rates are computed using actinic flux determined from a radiative transfer model. In this study, we compare predicted and measured nitrogen dioxide photolysis rate coefficients ( jNO 2). We used the Tropospheric Ultraviolet-Visible (TUV) radiation transfer model to predict jNO 2 values corresponding to measurements performed in Riverside, California as part of the 1997 Southern California Ozone Study (SCOS'97). Spectrally resolved irradiance measured at the same site allowed us to determine atmospheric optical properties, such as aerosol optical depth and total ozone column, that are needed as inputs for the radiative transfer model. Matching measurements of aerosol optical depth, ozone column, and jNO 2 were obtained for 14 days during SCOS'97. By using collocated measurements of the light extinction caused by aerosols and ozone over the full height of the atmosphere as model input, it was possible to predict sudden changes in jNO 2 resulting from atmospheric variability. While the diurnal profile of the rate coefficient was readily reproduced, jNO 2 model predicted values were found to be consistently higher than measured values. The bias between measured and predicted values was 17-36%, depending on the assumed single scattering albedo. By statistical analysis, we restricted the most likely values of the single scattering albedo to a range that produced bias on the order of 20-25%. It is likely that measurement error is responsible for a significant part of the bias. The aerosol single scattering albedo was found to be a major source of uncertainty in radiative transfer model predictions. Our best estimate indicates its average value at UV-wavelengths for the period of interest is between 0.77 and 0.85.

  10. Analysis of Mexico City urban air pollution using nitrogen dioxide column density measurements from UV/Visible spectroscopy

    NASA Astrophysics Data System (ADS)

    Garcia Payne, D. G.; Grutter, M.; Melamed, M. L.

    2010-12-01

    The differential optical absorption spectroscopy method (DOAS) was used to get column densities of nitrogen dioxide (NO2) from the analysis of zenith sky UV/visible spectra. Since the optical path length provides critical information in interpreting NO2 column densities, in conjunction with NO2 column densities, the oxygen dimer (O4) column density was retrieved to give insight into the optical path length. We report observations of year round NO2 and O4 column densities (from august 2009 to september 2010) from which the mean seasonal levels and the daily evolution, as well as the occurrence of elevated pollution episodes are examined. Surface nitric oxide (NO) and NO2 from the local monitoring network, as well as wind data and the vertical aerosol density from continuous Lidar measurements are used in the analysis to investigate specific events in the context of local emissions from vehicular traffic, photochemical production and transport from industrial emissions. The NO2 column density measurements will enhance the understanding Mexico City urban air pollution. Recent research has begun to unravel the complexity of the air pollution problem in Mexico City and its effects not only locally but on a regional and global scale as well.

  11. A Passive Sampler for Determination of Nitrogen Dioxide in Ambient Air

    ERIC Educational Resources Information Center

    Xiao, Dan; Lin, Lianzhi; Yuan, Hongyan; Choi, Martin M. F.; Chan, Winghong

    2005-01-01

    A passive sampler that provides a convenient, simple, and fast method for nitrogen dioxide determination is proposed. The experiment can be modified for determinations of other air pollutants like formaldehyde and sulfur dioxide for hands-on experience for students studying environmental pollution problems.

  12. 77 FR 64244 - Revision to Ambient Nitrogen Dioxide Monitoring Requirements

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-10-19

    ... monitoring requirements for the NO 2 monitoring network in support of the revised NO 2 NAAQS (75 FR 6474... the near-road component of the NO 2 monitoring network and to implement a phased deployment approach... example, in their public comments on the proposed primary NAAQS for NO 2 (74 FR 34404, July 15, 2012),...

  13. Nitrogen dioxide pollution in the Po basin: a quantitative analysis based on ground-based and satellite measurements

    NASA Astrophysics Data System (ADS)

    Petritoli, A.; Bonasoni, P.; Weiss, A.; Schaub, D.; Fortezza, F.

    2003-04-01

    Nitrogen dioxide (NO2) is an active nitrogen constituent playing a key role in tropospheric chemistry leading the photochemical production of ozone and influencing the concentration of the primary tropospheric oxidant, the hydroxyl radical (OH). The main source of tropospheric NO2 is the human activity so that it could be considered a pollutant for the atmosphere that is its concentration should be monitored and kept lower than threshold values. The use of measurements carried out from satellite platform could provide significant improvements to study and check the environmental pollution in a regional scale but an assessment of the quality of such measurements for tropospheric application is required. In this work we report in situ and tropospheric column measurements of NO2 in the Po-valley (the basin of the Po river in the northern Italy) region. The aim of the work was to provide a quantitative intercomparison between ground-based and satellite measurements and study the seasonal behaviour of the NO2 hot spot detected in the Po-valley. The study is carried out using in-situ chemiluminescent instrumentation installed in the Po-valley, a Uv/vis spectrometer installed at Mt. Cimone (44N, 11E) and tropospheric column measurements obtained from GOME (Global Ozone Monitoring Experiment) spectrometer. Results are presented and discussed.

  14. Improvements in the profiles and distributions of nitric acid and nitrogen dioxide with the LIMS version 6 dataset

    NASA Astrophysics Data System (ADS)

    Remsberg, E.; Natarajan, M.; Marshall, B. T.; Gordley, L. L.; Thompson, R. E.; Lingenfelser, G.

    2010-05-01

    The quality of the Nimbus 7 Limb Infrared Monitor of the Stratosphere (LIMS) nitric acid (HNO3) and nitrogen dioxide (NO2) profiles and distributions of 1978/1979 are described after their processing with an updated, Version 6 (V6) algorithm and subsequent archival in 2002. Estimates of the precision and accuracy of both of those species are developed and provided herein. The character of the V6 HNO3 profiles is relatively unchanged from that of the earlier LIMS Version 5 (V5) profiles, except in the upper stratosphere where the interfering effects of CO2 are accounted for better with V6. The accuracy of the retrieved V6 NO2 is also significantly better in the middle and upper stratosphere, due to improvements in its spectral line parameters and in the reduced biases for the accompanying V6 temperature and water vapor profiles. As a result of these important updates, there is better agreement with theoretical calculations for profiles of the HNO3/NO2 ratio, day-to-night NO2 ratio, and with estimates of the production of NO2 in the mesosphere and its descent to the upper stratosphere during polar night. In particular, the findings for middle and upper stratospheric NO2 should also be more compatible with those obtained from more recent satellite sensors because the effects of the spin-splitting of the NO2 lines are accounted for now with the LIMS V6 algorithm. The improved precisions and more frequent retrievals of the LIMS profiles along their orbit tracks provide for better continuity and detail in map analyses of these two species on pressure surfaces. It is judged that the chemical effects of the oxides of nitrogen on ozone can be studied quantitatively throughout the stratosphere with the LIMS V6 data.

  15. Evaluating the uncertainties of thermal catalytic conversion in measuring atmospheric nitrogen dioxide at four differently polluted sites in China

    NASA Astrophysics Data System (ADS)

    Xu, Zheng; Wang, Tao; Xue, L. K.; Louie, Peter K. K.; Luk, Connie W. Y.; Gao, J.; Wang, S. L.; Chai, F. H.; Wang, W. X.

    2013-09-01

    A widely used method for measuring nitrogen dioxide (NO2) in the atmosphere is the conversion of NO2 to nitric oxide (NO) on the hot surface of a molybdenum oxide (MoO) catalyst followed by the chemiluminescence detection of NO. Although it has long been recognized that this type of conversion may suffer from the positive interference of other oxidized nitrogen compounds, evaluations of such interference in the atmosphere are scarce, thus rendering it difficult to make use of a large portion of the NO2 or NOx data obtained via this method (often denoted as NO2* or NOx*). In the present study, we compared the MoO converter with a selective, more accurate photolytic approach at four differently polluted sites in China. The converter worked well at the urban site, which was greatly affected by fresh emissions, but, on average, overestimated NO2 by 30%-50% at the two suburban sites and by more than 130% at the mountain-top site during afternoon hours, with a much larger positive bias seen during the top 10% of ozone events. The degree of overestimation depended on both air-parcel age and the composition of the oxidation products/intermediates of NOx (NOz). We attempted to derive an empirical formula to correct for this overestimation using concurrently measured O3, NO, and NO2* at the two suburban sites. Although the formula worked well at each individual site, the different NOz partitions at the sites made it difficult to obtain a universal formula. In view of the difficulty of assessing the uncertainties of the conventional conversion method, thus limiting the usability of data obtained via this method in atmospheric research, we suggest that, in areas away from fresh NOx emission sources, either a more selective NO2 measurement method or a NOy (NOx and its reaction products and intermediates) instrument should be adopted.

  16. Nitrogen dioxide exposure and development of pulmonary emphysema

    SciTech Connect

    Stavert, D.M.; Archuleta, D.C.; Holland, L.M.; Lehnert, B.E.

    1986-01-01

    Lungs of adult Fischer-344 rats were evaluated for emphysematous changes after (1) a single intratracheal instillation of elastase (E), (2) a 25-d exposure to 35 ppm nitrogen dioxide (NO/sub 2/), and (3) elastase instillation followed by 25-d exposure to 35 ppm NO/sub 2/ (E + NO/sub 2/). Residual volumes (RV) of the NO/sub 2/ and NS groups were virtually identical, whereas the RV of the E and E + NO/sub 2/ lungs were significantly greater than those of the NS and NO/sub 2/ lungs. Directionally similar changes in the excised lung volumes and total lung capacities were obtained with the E and E + NO/sub 2/ groups; NO/sub 2/ alone, however, did not alter these volumetric parameters. No differences in arterial blood gases and pH values, minute ventilation, or breathing frequencies were found among the experimental groups. The mean linear intercept values (MLI) obtained with the NS and NO/sub 2/ exposed lungs were essentially identical with average values of approx. 62 ..mu..m. This morphometric parameter was substantially increased in the E- and E + NO/sub 2/-exposed lungs; no significant differences, however, were found between the MLI values obtained with the E and E + NO/sub 2/ lungs. From these data as well as histologic examinations of lung sections for evidence of emphysema, it was concluded that (1) a subchronic, moderately high level of NO/sub 2/ exposure does not produce an irreversible emphysematous lesion in the rat model and (2) exposure of rats to 35 ppm for 25 d after elastase instillation into the lungs does not potentiate protease-induced emphysema or bring about a progression in preexisting emphysema.

  17. Stratospheric nitrogen dioxide in Antarctic regions from ground based and satellite observations during 2001

    NASA Astrophysics Data System (ADS)

    Bortoli, Daniele; Giovanelli, Giorgio; Ravegnani, Fabrizio; Kostadinov, Ivan K.; Petritoli, Andrea; Calzolari, Francescopiero; Costa, Maria J.; Silva, Ana M.

    2003-04-01

    The application of Differential Optical Absorption Spectroscopy (DOAS) methodology to the zenith scattered light data collected with the GASCOD spectrometer developed at the ISAC Institute allow for the detection of stratospheric trace gases involved in the ozone cycle such as NO2, OClO, BrO. The instrument was installed in December 1995 in the Italian Antarctic station at Terra Nova Bay (74°26'S, 164°03E', Ross Sea), after several tests both in laboratory and in Antarctic region, for unattended and continuous measurement in extreme high-latitude environment. The GASCOD is still working and producing very interesting data for the study of the denitrification processes during the formation of the so-called ozone hole over the Antarctic region. For the continuous NO2 monitoring for whole the year, also during winter when the station is unmanned, the [407 - 460] nm spectral region is investigated. The results for Nitrogen Dioxide, obtained by application of DOAS algorithms to the data recorded during the year 2001, are presented. ERS-2 was launched in April 1995 into a near-polar sun-synchronous orbit at a mean altitude of 795 km. The descending node crosses the equator at 10:30 local time. GOME is a nadir-scanning double monochromator covering the 237 nm to 794 nm wavelength range with a spectral resolution of 0.17-0.33 nm. The spectrum is split into four spectral channels, each recorded quasi-simultaneously by a 1024-pixel photodiode array. The global spatial coverage is obtained within 3 days at the equator by a 960 km across-track swath (4.5 s forward scan, 1.5 s back scan). The ground pixel size of the measurements is 320 X 40 km2. A comparison of GASCOD and GOME results for NO2 total column is performed.

  18. An MCM modeling study of nitryl chloride (ClNO2) impacts on oxidation, ozone production and nitrogen oxide partitioning in polluted continental outflow

    NASA Astrophysics Data System (ADS)

    Riedel, T. P.; Wolfe, G. M.; Danas, K. T.; Gilman, J. B.; Kuster, W. C.; Bon, D. M.; Vlasenko, A.; Li, S.-M.; Williams, E. J.; Lerner, B. M.; Veres, P. R.; Roberts, J. M.; Holloway, J. S.; Lefer, B.; Brown, S. S.; Thornton, J. A.

    2013-11-01

    Nitryl chloride (ClNO2) is produced at night by reactions of dinitrogen pentoxide (N2O5) on chloride containing surfaces. ClNO2 is photolyzed during the morning hours after sunrise to liberate highly reactive chlorine atoms (Cl·). This chemistry takes place primarily in polluted environments where the concentrations of N2O5 precursors (nitrogen oxide radicals and ozone) are high, though it likely occurs in remote regions at lower intensities. Recent field measurements have illustrated the potential importance of ClNO2 as a daytime Cl· source and a nighttime NOx reservoir. However, the fate of the Cl· and the overall impact of ClNO2 on regional photochemistry remain unclear. To this end, we have incorporated ClNO2 production, photolysis, and subsequent Cl· reactions into an existing Master Chemical Mechanism (MCM version 3.2) box model framework using observational constraints from the CalNex 2010 field study. Cl· reactions with a set of alkenes and alcohols, and the simplified multiphase chemistry of N2O5, ClNO2, HOCl, ClONO2, and Cl2, none of which are currently part of the MCM, have been added to the mechanism. The presence of ClNO2 produces significant changes to oxidants, ozone, and nitrogen oxide partitioning, relative to model runs excluding ClNO2 formation. From a nighttime maximum of 1.5 ppbv ClNO2, the daytime maximum Cl· concentration reaches 1 × 105 atoms cm-3 at 7 a.m., reacting mostly with a large suite of volatile organic compounds (VOC) to produce 2.2 times more organic peroxy radicals in the morning than in the absence of ClNO2. In the presence of several ppbv of nitrogen oxide radicals (NOx = NO + NO2), these perturbations lead to similar enhancements in hydrogen oxide radicals (HOx = OH + HO2). Neglecting contributions from HONO, the total integrated daytime radical source is 17% larger when including ClNO2, which leads to a similar enhancement in integrated ozone production of 15%. Detectable levels (tens of pptv) of chlorine containing

  19. An MCM modeling study of nitryl chloride (ClNO2) impacts on oxidation, ozone production and nitrogen oxide partitioning in polluted continental outflow

    NASA Astrophysics Data System (ADS)

    Riedel, T. P.; Wolfe, G. M.; Danas, K. T.; Gilman, J. B.; Kuster, W. C.; Bon, D. M.; Vlasenko, A.; Li, S.-M.; Williams, E. J.; Lerner, B. M.; Veres, P. R.; Roberts, J. M.; Holloway, J. S.; Lefer, B.; Brown, S. S.; Thornton, J. A.

    2014-04-01

    Nitryl chloride (ClNO2) is produced at night by reactions of dinitrogen pentoxide (N2O5) on chloride containing surfaces. ClNO2 is photolyzed during the morning hours after sunrise to liberate highly reactive chlorine atoms (Cl·). This chemistry takes place primarily in polluted environments where the concentrations of N2O5 precursors (nitrogen oxide radicals and ozone) are high, though it likely occurs in remote regions at lower intensities. Recent field measurements have illustrated the potential importance of ClNO2 as a daytime Cl· source and a nighttime NOx reservoir. However, the fate of the Cl· and the overall impact of ClNO2 on regional photochemistry remain poorly constrained by measurements and models. To this end, we have incorporated ClNO2 production, photolysis, and subsequent Cl· reactions into an existing master chemical mechanism (MCM version 3.2) box model framework using observational constraints from the CalNex 2010 field study. Cl· reactions with a set of alkenes and alcohols, and the simplified multiphase chemistry of N2O5, ClNO2, HOCl, ClONO2, and Cl2, none of which are currently part of the MCM, have been added to the mechanism. The presence of ClNO2 produces significant changes to oxidants, ozone, and nitrogen oxide partitioning, relative to model runs excluding ClNO2 formation. From a nighttime maximum of 1.5 ppbv ClNO2, the daytime maximum Cl· concentration reaches 1 × 105 atoms cm-3 at 07:00 model time, reacting mostly with a large suite of volatile organic compounds (VOC) to produce 2.2 times more organic peroxy radicals in the morning than in the absence of ClNO2. In the presence of several ppbv of nitrogen oxide radicals (NOx = NO + NO2), these perturbations lead to similar enhancements in hydrogen oxide radicals (HOx = OH + HO2). Neglecting contributions from HONO, the total integrated daytime radical source is 17% larger when including ClNO2, which leads to a similar enhancement in integrated ozone production of 15%. Detectable

  20. A broadband cavity enhanced absorption spectrometer for aircraft measurements of glyoxal, methylglyoxal, nitrous acid, nitrogen dioxide, and water vapor

    NASA Astrophysics Data System (ADS)

    Min, K.-E.; Washenfelder, R. A.; Dubé, W. P.; Langford, A. O.; Edwards, P. M.; Zarzana, K. J.; Stutz, J.; Lu, K.; Rohrer, F.; Zhang, Y.; Brown, S. S.

    2015-10-01

    We describe a two-channel broadband cavity enhanced absorption spectrometer (BBCEAS) for aircraft measurements of glyoxal (CHOCHO), methylglyoxal (CH3COCHO), nitrous acid (HONO), nitrogen dioxide (NO2), and water (H2O). The instrument spans 361-389 and 438-468 nm, using two light emitting diodes (LEDs) and a grating spectrometer with a charge-coupled device (CCD) detector. Robust performance is achieved using a custom optical mounting system, high power LEDs with electronic on/off modulation, state-of-the-art cavity mirrors, and materials that minimize analyte surface losses. We have successfully deployed this instrument during two aircraft and two ground-based field campaigns to date. The demonstrated precision (2σ) for retrievals of CHOCHO, HONO and NO2 are 34, 350 and 80 pptv in 5 s. The accuracy is 5.8, 9.0 and 5.0 % limited mainly by the available absorption cross sections.

  1. A broadband cavity enhanced absorption spectrometer for aircraft measurements of glyoxal, methylglyoxal, nitrous acid, nitrogen dioxide, and water vapor

    NASA Astrophysics Data System (ADS)

    Min, K.-E.; Washenfelder, R. A.; Dubé, W. P.; Langford, A. O.; Edwards, P. M.; Zarzana, K. J.; Stutz, J.; Lu, K.; Rohrer, F.; Zhang, Y.; Brown, S. S.

    2016-02-01

    We describe a two-channel broadband cavity enhanced absorption spectrometer (BBCEAS) for aircraft measurements of glyoxal (CHOCHO), methylglyoxal (CH3COCHO), nitrous acid (HONO), nitrogen dioxide (NO2), and water (H2O). The instrument spans 361-389 and 438-468 nm, using two light-emitting diodes (LEDs) and a single grating spectrometer with a charge-coupled device (CCD) detector. Robust performance is achieved using a custom optical mounting system, high-power LEDs with electronic on/off modulation, high-reflectivity cavity mirrors, and materials that minimize analyte surface losses. We have successfully deployed this instrument during two aircraft and two ground-based field campaigns to date. The demonstrated precision (2σ) for retrievals of CHOCHO, HONO and NO2 are 34, 350, and 80 parts per trillion (pptv) in 5 s. The accuracy is 5.8, 9.0, and 5.0 %, limited mainly by the available absorption cross sections.

  2. Formation of strong airway irritants in mixtures of isoprene/ozone and isoprene/ozone/nitrogen dioxide.

    PubMed Central

    Wilkins, C K; Clausen, P A; Wolkoff, P; Larsen, S T; Hammer, M; Larsen, K; Hansen, V; Nielsen, G D

    2001-01-01

    We evaluated the airway irritation of isoprene, isoprene/ozone, and isoprene/ozone/nitrogen dioxide mixtures using a mouse bioassay, from which we calculated sensory irritation, bronchial constriction, and pulmonary irritation. We observed significant sensory irritation (approximately 50% reduction of mean respiratory rate) by dynamically exposing the mice, over 30 min, to mixtures of isoprene and O3 or isoprene, O3, and NO2. The starting concentrations were approximately 4 ppm O3 and 500 ppm isoprene (+ approximately 4 ppm NO2. The reaction mixtures after approximately 30 sec contained < 0.2 ppm O3. Addition of the effects of the residual reactants and the identified stable irritant products (formaldehyde, formic acid, acetic acid, methacrolein, and methylvinyl ketone) could explain only partially the observed sensory irritation. This suggests that one or more strong airway irritants were formed. It is thus possible that oxidation reactions of common unsaturated compounds may be relevant for indoor air quality. PMID:11673123

  3. Theoretical study of the hydrogen abstraction of substituted phenols by nitrogen dioxide as a source of HONO.

    PubMed

    Shenghur, Abraham; Weber, Kevin H; Nguyen, Nhan D; Sontising, Watit; Tao, Fu-Ming

    2014-11-20

    The mild yet promiscuous reactions of nitrogen dioxide (NO2) and phenolic derivatives to produce nitrous acid (HONO) have been explored with density functional theory calculations. The reaction is found to occur via four distinct pathways with both proton coupled electron transfer (PCET) and hydrogen atom transfer (HAT) mechanisms available. While the parent reaction with phenol may not be significant in the gas phase, electron donating groups in the ortho and para positions facilitate the reduction of nitrogen dioxide by electronically stabilizing the product phenoxy radical. Hydrogen bonding groups in the ortho position may additionally stabilize the nascent resonantly stabilized radical product, thus enhancing the reaction. Catechol (ortho-hydroxy phenol) has a predicted overall free energy change ΔG(0) = -0.8 kcal mol(-1) and electronic activation energy Ea = 7.0 kcal mol(-1). Free amines at the ortho and para positions have ΔG(0) = -3.8 and -1.5 kcal mol(-1); Ea = 2.3 and 2.1 kcal mol(-1), respectively. The results indicate that the hydrogen abstraction reactions of these substituted phenols by NO2 are fast and spontaneous. Hammett constants produce a linear correlation with bond dissociation energy (BDE) demonstrating that the BDE is the main parameter controlling the dark abstraction reaction. The implications for atmospheric chemistry and ground-level nitrous acid production are discussed. PMID:25325182

  4. Revealing the Origin of Activity in Nitrogen-Doped Nanocarbons towards Electrocatalytic Reduction of Carbon Dioxide.

    PubMed

    Xu, Junyuan; Kan, Yuhe; Huang, Rui; Zhang, Bingsen; Wang, Bolun; Wu, Kuang-Hsu; Lin, Yangming; Sun, Xiaoyan; Li, Qingfeng; Centi, Gabriele; Su, Dangsheng

    2016-05-23

    Carbon nanotubes (CNTs) are functionalized with nitrogen atoms for reduction of carbon dioxide (CO2 ). The investigation explores the origin of the catalyst's activity and the role of nitrogen chemical states therein. The catalysts show excellent performances, with about 90 % current efficiency for CO formation and stability over 60 hours. The Tafel analyses and density functional theory calculations suggest that the reduction of CO2 proceeds through an initial rate-determining transfer of one electron to CO2 , which leads to the formation of carbon dioxide radical anion (CO2 (.-) ). The initial reduction barrier is too high on pristine CNTs, resulting in a very high overpotentials at which the hydrogen evolution reaction dominates over CO2 reduction. The doped nitrogen atoms stabilize the radical anion, thereby lowering the initial reduction barrier and improving the intrinsic activity. The most efficient nitrogen chemical state for this reaction is quaternary nitrogen, followed by pyridinic and pyrrolic nitrogen. PMID:27100272

  5. Sub-ambient carbon dioxide adsorption properties of nitrogen doped graphene

    SciTech Connect

    Tamilarasan, P.; Ramaprabhu, Sundara

    2015-04-14

    Carbon dioxide adsorption on carbon surface can be enhanced by doping the surface with heterogeneous atoms, which can increase local surface affinity. This study presents the carbon dioxide adsorption properties of nitrogen doped graphene at low pressures (<100 kPa). Graphene was exposed to nitrogen plasma, which dopes nitrogen atoms into carbon hexagonal lattice, mainly in pyridinic and pyrrolic forms. It is found that nitrogen doping significantly improves the CO{sub 2} adsorption capacity at all temperatures, due to the enrichment of local Lewis basic sites. In general, isotherm and thermodynamic parameters suggest that doped nitrogen sites have nearly same adsorption energy of surface defects and residual functional groups. The isosteric heat of adsorption remains in physisorption range, which falls with surface coverage, suggesting the distribution of magnitude of adsorption energy. The absolute values of isosteric heat and entropy of adsorption are slightly increased upon nitrogen doping.

  6. OMI Total and Tropospheric Column Nitrogen Dioxide: Version 2 Status

    NASA Technical Reports Server (NTRS)

    Gleason, James

    2007-01-01

    The at-launch version of the OM1 NO2 total and tropospheric NO2 algorithm made a number of assumptions about instrument performance. Our knowledge of tropospheric NO2 has increased in the 3 years since the inital version was delivered. The results of the post-launch validation campaigns and improved atmospheric modelling has lead to changes in the NO2 retrieval algorithm. The algorithm changes and the impacts on the data products will be presented.

  7. 78 FR 16184 - Revision to Ambient Nitrogen Dioxide Monitoring Requirements

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-03-14

    ... Network Implementation We are finalizing a phased implementation approach, as proposed (77 FR 64244), to... the near-road component of the NO 2 monitoring network in order to implement a phased deployment... the revised NO 2 NAAQS (75 FR 6474). The NO 2 NAAQS was revised to include a 1-hour standard with...

  8. FATE OF INHALED NITROGEN DIOXIDE IN ISOLATED PERFUSED RAT LUNG

    EPA Science Inventory

    The fate of inhaled NO2 was studied with isolated perfused rat lungs. The isolated lungs were exposed to 5 ppm NO2 for 90 min at a ventilation rate of 45 ml/min. The NO2 exposure had no adverse effects on the lungs as judged from their weights, glucose uptake, or lactate producti...

  9. MAX-DOAS measurements of nitrogen dioxide at the high altitude sites Zugspitze (2964 m) and Pico Espejo (4765 m)

    NASA Astrophysics Data System (ADS)

    Schreier, Stefan F.; Richter, Andreas; Wittrock, Folkard; Burrows, John P.

    2015-04-01

    Spectral measurements at two mountain sites were performed with a MAX-DOAS (Multi AXis Differential Optical Absorption Spectroscopy) instrument from February to July 2003 (Zugspitze, Germany) and from March 2004 to November 2008 (Pico Espejo, Venezuela). Here, these measurements are used for the retrieval of slant column densities (SCDs) of nitrogen dioxide (NO2). While at the altitude of observations the NO2 levels are usually small, uplifting of anthropogenic emissions from the valley and in Venezuela also transport of emissions from biomass burning can lead to significant enhancements. Daily, weekly, and seasonal cycles of NO2 SCDs are shown for the two stations, linked to different meteorological conditions and compared between the two sites. In a next step, a preliminary approach to derive vertical column densities (VCDs) is presented. VCDs of NO2 from ground-based MAX-DOAS instruments provide useful information for the validation of satellite instruments such as SCIAMACHY, OMI, and GOME-2. Comparisons between ground-based and satellite-based NO2 VCDs are shown for selected periods.

  10. Effects of nitrogen dioxide on growth and yield of black turtle bean (Phaseolus vulgaris L.) cv. 'Domino'.

    PubMed

    Sandhu, R; Gupta, G

    1989-01-01

    Twenty-six-day-old black turtle bean cv. 'Domino' plants were exposed to nitrogen dioxide (0.0, 0.025, 0.05 and 0.10 microl liter(-1)), 7 h per day for 5 days per week for 3 weeks, under controlled environment. Data were collected on net photosynthesis rate (PN), stomatal resistance (SR), and dark respiration rate (DR), immediately after exposure, 24 h after the termination of exposure and at maturity (when the leaves had just started turning yellow), using a LICOR 6000 Portable Photosynthesis System. Chlorophyll-a (Ch-a), chlorophyll-b (Ch-b), total chlorophyll (tot-Ch) and leaf nitrogen were measured immediately after exposure and at maturity. Growth characteristics-relative growth rate (RGR), net assimilation rate (NAR), leaf area ratio (LAR) and root: shoot ratio (RSR)-were computed for treated plants. Net photosynthesis rate increased by 53% in 0.10 microl liter(-1) NO2 treated plants immediately after exposure compared to control plants. Dark respiration rates were also higher in treated plants. Ch-a, Ch-b and tot-Ch showed significant increases with 0.1 microl liter(-1) NO2 treatment immediately after exposure. Foliar nitrogen content showed an increase in treated plants both immediately after exposure and at maturity. Increases were also seen in RGR and NAR. Plant yield increased by 86% (number of pods), 29% (number of seeds) and 46% (weight of seeds), respectively. Nitrogen dioxide stimulated the overall plant growth and crop yield. PMID:15092401

  11. The effects of rapid urbanization on the levels in tropospheric nitrogen dioxide and ozone over East China

    NASA Astrophysics Data System (ADS)

    Huang, Jianping; Zhou, Chenhong; Lee, Xuhui; Bao, Yunxuan; Zhao, Xiaoyan; Fung, Jimmy; Richter, Andreas; Liu, Xiong; Zheng, Yiqi

    2013-10-01

    Over the past few decades, China has experienced a rapid increase in urbanization. The urban built-up areas (population) in Beijing, Shanghai, and Guangzhou increased by 197% (87%), 148% (65%), and 273% (25%), respectively, from 1996 to 2011. We use satellite retrieval data to quantify the effects of rapid urbanization on the yearly and seasonal changes in tropospheric nitrogen dioxide (NO2) over East China. The results show that rapid urbanization has a profound effect on tropospheric columns of NO2. During 1996-2011, the tropospheric columns of NO2 over the surrounding areas of Guangzhou, Shanghai, and Beijing increased by 82%, 292%, and 307%, respectively. The tropospheric columns of NO2 reach their maximum in winter and minimum in spring. The anthropogenic emissions related to urbanization are a dominant factor in the long-term changes in the yearly and seasonal mean tropospheric columns of NO2, whereas meteorological conditions such as the prevailing winds and precipitation account for the unique spatial patterns. Around the time of the 2008 Beijing Olympic Games, the tropospheric columns of NO2 over Beijing urban area significantly reduced by 48% in July, 35% in August, and 49% in September, relative to the same monthly averages over 2005-2007. However, this trend was reversed after the Games, and the increased rate was even larger than before. Our results show that the tropospheric NO2 above the three regions increased at rates 1.3-8 times faster than the rates in a recent inventory estimate of NOx emissions for 2000-2010. We also discuss the influence of urbanization on tropospheric ozone and find that the Ozone Monitoring Instrument (OMI) retrieval tropospheric column shows that ozone levels are relatively insensitive to urbanization and changes in tropospheric NO2.

  12. Carbon Monoxide, Nitric Oxide, and Nitrogen Dioxide Levels in Gas Ovens Related to Surface Pinking of Cooked Beef and Turkey.

    PubMed

    Cornforth; Rabovitser; Ahuja; Wagner; Hanson; Cummings; Chudnovsky

    1998-01-19

    Carbon monoxide (CO) and total nitrogen oxide (NO(x)()) levels were monitored during meat cookery with a standard Ovenpak and a new ultralow-NO(x)() (ULN) cyclonic gas burner. With the standard burner, CO varied from 103 to 152 ppm, NO(x)() was 1.3-10.7 ppm, and surface pinking was observed on both beef and turkey. The ULN burner at optimal efficiency produced only 6.7 ppm of CO and 1 ppm of NO(x)(), insufficient to cause surface pinking. To determine the relative contribution of CO and NO(x)() to pinking, trials were also conducted in an electric oven with various pure gases. Pinking was not observed with up to 149 ppm of CO or 5 ppm of NO. However, as little as 0.4 ppm of nitrogen dioxide (NO(2)) caused pinking of turkey rolls. Beef roasts were pink at >2.5 ppm of NO(2). Thus, pinking previously attributed to CO and NO in gas ovens is instead due to NO(2), which has much greater reactivity than NO with moisture at meat surfaces. PMID:10554228

  13. Response of needle sulphur and nitrogen concentrations of Scots pine versus Norway spruce to SO2 and NO2.

    PubMed

    Manninen, S; Huttunen, S

    2000-03-01

    The results of two field studies and an open-top chamber fumigation experiment showed that the response of mature Scots pine to SO(2) and NO(2) differed from that of mature Norway spruce. Moreover, the response of pine seedlings to SO(2) and NO(2) differed from that of mature trees. The greater increase in the needle total S concentrations of pine suggested more abundant stomatal uptake of SO(2) compared to spruce. Both pine seedlings and mature trees also seemed to absorb more N from atmospheric deposition. Mature pine was able to assimilate SO(4)(2-) derived from SO(2) into organic S more effectively than mature spruce at the high S and N deposition sites, whereas both pine and spruce seedlings accumulated SO(4)-S under NO(2)+SO(2) exposure. Spruce, in turn, accumulated SO(4)-S even when well supplied with N. Net assimilation of SO(4)(2-) in conifer seedlings was enhanced markedly by elevated temperature. To protect the northern coniferous forests against the harmful effects of S and N deposition, it is recommended that the critical level for SO(2) as a growing season mean be set at 5-10 microg m(-3) and NO(2) at 10-15 microg m(-3), depending on the 'effective temperature sum' and/or whether SO(2) and NO(2) occur alone or in combination. PMID:15092988

  14. Product selectivity of visible-light photocatalytic reduction of carbon dioxide using titanium dioxide doped by different nitrogen-sources

    NASA Astrophysics Data System (ADS)

    Zhang, Zhaoguo; Huang, Zhengfeng; Cheng, Xudong; Wang, Qingli; Chen, Yi; Dong, Peimei; Zhang, Xiwen

    2015-11-01

    The influence of nitrogen-source on the photocatalytic properties of nitrogen-doped titanium dioxide is herein first investigated from the perspective of the chemical bond form of the nitrogen element in the nitrogen-source. The definitive role of groups such as Nsbnd N from the nitrogen-source on the surface of as-prepared samples in the selectivity of the dominant product of photocatalytic reduction is demonstrated. Well-crystallized one-dimensional Nsbnd TiO2 nanorod arrays with a preferred orientation of the rutile (3 1 0) facet are manufactured via a hydrothermal treatment using hydrazine and ammonia variously as the source of nitrogen. Significant selectivity of the dominant reduced products has been exhibited for Nsbnd TiO2 prepared from different nitrogen-sources in carbon dioxide photocatalytic reduction under visible light illumination. CH4 is the main product with N2H4-doped Nsbnd TiO2, while CO is the main product with NH3-doped Nsbnd TiO2, which can be attributed to the existence of the reducing Nsbnd N groups in the N2H4-doped Nsbnd TiO2 surfaces after the hydrothermal treatment. Compared with the approaches previously reported, the facile one-step route utilized here accomplishes the fabrication of Nsbnd TiO2 possessing visible-light activity and attainment of selectivity of dominant photocatalytic reduction product simultaneously by choosing a nitrogen-source with appropriate chemical bond form, which provides a completely new approach to understanding the effects of doping treatment on photocatalytic properties.

  15. Computation of Bond Dissociation Energies for Removal of Nitrogen Dioxide Groups in Certain Aliphatic Nitro Compounds

    NASA Astrophysics Data System (ADS)

    Shao, Ju-Xiang; Cheng, Xin-Lu; Yang, Xiang-Dong; Xiang, Shi-Kai

    2006-04-01

    Bond dissociation energies for removal of nitrogen dioxide groups in 10 aliphatic nitro compounds, including nitromethane, nitroethylene, nitroethane, dinitromethane, 1-nitropropane, 2-nitropropane, 1-nitrobutane, 2-methyl-2-nitropropane, nitropentane, and nitrohexane, are calculated using the highly accurate complete basis set (CBS-Q) and the three hybrid density functional theory (DFT) methods B3LYP, B3PW91 and B3P86 with 6-31G** basis set. By comparing the computed bond dissociation energies and experimental results, we find that the B3LYP/6-31G** and B3PW91/6-31G** methods are incapable of predicting the satisfactory bond dissociation energy (BDE). However, B3P86/6-31G** and CBS-Q computations are capable of giving the calculated BDEs, which are in extraordinary agreement with the experimental data. Nevertheless, since CBS-Q computational demands increase rapidly with the number of containing atoms in molecules, larger molecules soon become prohibitively expensive. Therefore, we suggest to take the B3P86/6-31G** method as a reliable method of computing the BDEs for removal of the NO2 groups in the aliphatic nitro compounds.

  16. Personal exposure to nitrogen dioxide and its association with respiratory illness in Hong Kong

    SciTech Connect

    Koo, L.C.; Ho, J.H.; Ho, C.Y.; Matsuki, H.; Shimizu, H.; Mori, T.; Tominaga, S. )

    1990-05-01

    In 1985, 362 primary schoolchildren and their 319 mothers were surveyed in Hong Kong to study the possible relationship of air pollution to respiratory illnesses. Using nitrogen dioxide (NO{sub 2}) measured by personal samplers as a measure of air pollution, the study aimed to identify the major sources of NO{sub 2} in the indoor environment and see whether its increased presence was associated with respiratory symptoms. The levels of NO{sub 2} among the mothers was found to increase by 21% if dust exposure was reported from the workplace, 18% if they used such cooking fuels as liquid petroleum gas or kerosene, 11% when kitchens did not have ventilating fans, and 10% when incense was burned at home. In terms of respiratory symptoms, an increase in NO{sub 2} levels of 19% was reported among those with allergic rhinitis and 18% among those with chronic cough. The levels of NO2 among children were correlated with levels measured in classrooms, all of which had opened windows so that the NO{sub 2} came from outdoors. No association was found between children's NO{sub 2} levels and respiratory symptoms. With the exception of smoking by the father and the children's NO{sub 2} levels, no association was found between smoking at home and NO{sub 2} levels.

  17. Development and transferability of a nitrogen dioxide land use regression model within the Veneto region of Italy

    NASA Astrophysics Data System (ADS)

    Marcon, Alessandro; de Hoogh, Kees; Gulliver, John; Beelen, Rob; Hansell, Anna L.

    2015-12-01

    When measurements or other exposure models are unavailable, air pollution concentrations could be estimated by transferring land-use regression (LUR) models from other areas. No studies have looked at transferability of LUR models from regions to cities. We investigated model transferability issues. We developed a LUR model for 2010 using annual average nitrogen dioxide (NO2) concentrations retrieved from 47 regulatory stations of the Veneto region, Northern Italy. We applied this model to 40 independent sites in Verona, a city inside the region, where NO2 had been monitored in the European Study of Cohorts for Air Pollution Effects (ESCAPE) during 2010. We also used this model to estimate average NO2 concentrations at the regulatory network in 2008, 2009 and 2011. Of 33 predictor variables offered, five were retained in the LUR model (R2 = 0.75). The number of buildings in 5000 m buffers, industry surface area in 1000 m buffers and altitude, mainly representing large-scale air pollution dispersion patterns, explained most of the spatial variability in NO2 concentrations (R2 = 0.68), while two local traffic proxy indicators explained little of the variability (R2 = 0.07). The performance of this model transferred to urban sites was poor overall (R2 = 0.18), but it improved when only predicting inner-city background concentrations (R2 = 0.52). Recalibration of LUR coefficients improved model performance when predicting NO2 concentrations at the regulatory sites in 2008, 2009 and 2011 (R2 between 0.67 and 0.80). Models developed for a region using NO2 regulatory data are unable to capture small-scale variability in NO2 concentrations in urban traffic areas. Our study documents limitations in transferring a regional model to a city, even if it is nested within that region.

  18. Signature of tropospheric ozone and nitrogen dioxide from space: A case study for Athens, Greece

    NASA Astrophysics Data System (ADS)

    Varotsos, C.; Christodoulakis, J.; Tzanis, C.; Cracknell, A. P.

    2014-06-01

    The aim of the present study is to investigate the variability of the tropospheric ozone and nitrogen dioxide (NO2) columns over mainland Greece, by using observations carried out by satellite-borne instrumentation and Multi Sensor Reanalysis. The results obtained show that the tropospheric ozone residual (TOR) dispersed farther away than the tropospheric NO2 column (TNO), due to the longer TOR's lifetime in respect to that of TNO. This results in the influence of the air quality of the nearby southern islands from the air pollution of the greater Athens basin. Furthermore, the TOR and TNO columns over Athens, for the period October 2004 to December 2011 were found to be negatively correlated with a correlation coefficient -0.85, in contrast to recent findings which suggested strong positive correlation. Interestingly, this strong negative correlation into a slight positive correlation when the TNO concentration becomes higher than around 4 × 1015 molec cm-2, thus being best fitted by a quadratic relationship. In addition, the temporal evolution of TOR during 1979-1993 showed a decline of 0.2% per decade and just after 1993 it seems to obey a positive trend of 0.1% per decade, thus recovering during the period 1993-2011 almost 63% of the lost TOR amounts through the years 1979-1993. Finally, the association between TOR, the total ozone column (TOZ), the tropopause height and the outgoing longwave radiation (OLR) is presented by analysing observations during 1979-2011. An unexpected positive correlation between OLR and TOR was found, which may probably be attributed to the fact that enhanced abundance in tropospheric water vapor reduces the summertime TOR maximum by destructing ozone in the lower and middle troposphere through uptake mechanisms, thus emitting higher amounts of longwave radiation upwards.

  19. Indoor-outdoor relationships of airborne particles and nitrogen dioxide inside Parisian buses

    NASA Astrophysics Data System (ADS)

    Molle, Romain; Mazoué, Sophie; Géhin, Évelyne; Ionescu, Anda

    2013-04-01

    This study evaluated passengers' exposure to traffic air pollution inside the articulated buses of the line 91 in Paris during 10 working days in May, 2010. Twenty articulated buses were studied on 32 routes in order to determine the influence of the sampling position on the pollutant concentrations. This parameter is still poorly known for the rigid buses and is even less known for the articulated ones. However this parameter must be studied for articulated buses because the greater length may cause a pollutant concentration gradient in the cabin. Portable devices were used to measure pollutants in the presence of passengers from 8 a.m. to 9 a.m. and from 4 p.m. to 5 p.m., time periods corresponding to the peak traffic and travellers. PM2.5 mass concentration, particle number concentration between 0.3 and 20 μm and nitrogen dioxide concentration were simultaneously measured on three positions inside the buses (front, middle and rear) in order to study the spatial distribution of these compounds. These measurements inside the buses were compared to the outdoor concentrations at the same moment of the day provided by the Parisian air quality monitoring network; they were also compared to the results of a previous monitoring campaign performed in 2008. The results obtained during the 2010 campaign revealed that in-cabin NO2 mean concentrations were 1.5-3.5 times higher than the outside concentration levels; a maximum concentration of 234 ± 40 μg m-3 was found in the rear position (location of the engine and exhaust gas). Mean in-cabin PM2.5 mass concentrations varied from one week to another one, but they were globally the same at the three positions inside the instrumented buses. In order to determine the impact of outdoor levels, correlations have been calculated between the results measured inside the buses and those measured by the outdoor air monitoring stations. The highest Pearson correlation coefficient was 0.29 for NO2 data whereas the highest Pearson

  20. Broadband cavity enhanced spectroscopy in the ultraviolet spectral region for measurements of nitrogen dioxide and formaldehyde

    NASA Astrophysics Data System (ADS)

    Washenfelder, R. A.; Attwood, A. R.; Flores, J. M.; Rudich, Y.; Brown, S. S.

    2015-09-01

    Formaldehyde (CH2O) is the most abundant aldehyde in the atmosphere, and strongly affects photochemistry through its photolysis. We describe simultaneous measurements of CH2O and nitrogen dioxide (NO2) using broadband cavity enhanced spectroscopy in the ultraviolet spectral region. The light source consists of a continuous-wave diode laser focused into a Xenon bulb to produce a plasma that emits high-intensity, broadband light. The plasma discharge is optically filtered and coupled into a 1 m optical cavity. The reflectivity of the cavity mirrors is 0.99933 ± 0.00003 (670 ppm loss) at 338 nm, as determined from the known Rayleigh scattering of He and zero air. This mirror reflectivity corresponds to an effective path length of 1.49 km within the 1 m cell. We measure the cavity output over the 315-350 nm spectral region using a grating monochromator and charge-coupled device (CCD) array detector. We use published reference spectra with spectral fitting software to simultaneously retrieve CH2O and NO2 concentrations. Independent measurements of NO2 standard additions by broadband cavity enhanced spectroscopy and cavity ringdown spectroscopy agree within 2 % (slope for linear fit = 0.98 ± 0.03 with r2 = 0.998). Standard additions of CH2O measured by broadband cavity enhanced spectroscopy and calculated based on flow dilution are also well-correlated, with r2 = 0.9998. During constant, mixed additions of NO2 and CH2O, the 30 s measurement precisions (1σ) of the current configuration were 140 and 210 pptv, respectively. The current 1-min detection limit for extinction measurements at 315-350 nm provides sufficient sensitivity for measurement of trace gases in laboratory experiments and ground-based field experiments. Additionally, the instrument provides highly accurate, spectroscopically-based trace gas detection that may complement higher precision techniques based on non-absolute detection methods. In addition to trace gases, this approach will be appropriate for

  1. Concentrations of nitrogen dioxide throughout the state of Bahrain.

    PubMed

    Danish, S; Madany, I M

    1992-01-01

    A comprehensive field study of atmospheric NO2 was conducted throughout the state of Bahrain, using passive diffusion tube samplers. A total of 319 tubes were used, and all sites were chosen to include residential, heavy and low traffic roads, industrial, airport and commercial areas. The results of the survey revealed marked spatial variations in NO2 concentrations. The weekly mean NO2 values varied from 76 microg m(-3) in the north-eastern part of Bahrain island to 13 microg m(-3) in the south-east of Muharaq island. Generally, NO2 values decreased from the north to the south, where traffic volume and density also decreased. In addition, the results indicated that high traffic areas revealed higher NO2 levels compared with airport and industrial areas. The highest NO2 concentrations were measured in roads characterized by being narrow and confined, with many traffic lights and roundabouts, indicating the influence of road geometry on NO2 levels. The results provide valuable baseline information for future investigators, especially since the study was conducted at the start of the Gulf War, which was accompanied by substantial emissions of NO2 from jet fighters and burning of about 600 oil fields. PMID:15091980

  2. Nitrogen Dioxide Exposure and Airway Responsiveness in Individuals with Asthma

    EPA Science Inventory

    Controlled human exposure studies evaluating the effect of inhaled NO2 on the inherent responsiveness of the airways to challenge by bronchoconstricting agents have had mixed results. In general, existing meta-analyses show statistically significant effects of NO2 on the airway r...

  3. Improvements in the profiles and distributions of nitric acid and nitrogen dioxide with the LIMS version 6 dataset

    NASA Astrophysics Data System (ADS)

    Remsberg, E.; Natarajan, M.; Marshall, T.; Gordley, L. L.; Thompson, R. E.; Lingenfelser, G.

    2010-02-01

    The quality of the Nimbus 7 Limb Infrared Monitor of the Stratosphere (LIMS) nitric acid (HNO3) and nitrogen dioxide (NO2) profiles and distributions of 1978/1979 is described after their processing with an updated, Version 6 (V6) algorithm and subsequent archival in 2002. Estimates of the precision and accuracy of both of those species are developed and provided herein. The character of the V6 HNO3 profiles is relatively unchanged from that of the earlier LIMS Version 5 (V5) profiles, except in the upper stratosphere where the interfering effects of CO2 are accounted for better with V6. The accuracy of the retrieved V6 NO2 is also significantly better in the middle and upper stratosphere, due to improvements in its spectral line parameters and in the reduced biases for the accompanying V6 temperature and water vapor profiles. As a result of these important updates, there is better agreement with theoretical calculations for profiles of the HNO3/NO2 ratio, day-to-night NO2 ratio, and with estimates of the production of NO2 in the mesosphere and its descent to the upper stratosphere during polar night. The improved precisions and more frequent retrievals of the profiles along the LIMS orbit tracks provide for better continuity and detail in map analyses of these two species on pressure surfaces. It is judged that the chemical effects of the oxides of nitrogen on ozone can be examined quantitatively throughout the stratosphere with the LIMS V6 data, and that the findings will be more compatible with those obtained from measurements of the same species from subsequent satellite sensors.

  4. Measurement of nitrogen dioxide diffusive sampling rates for Palmes diffusion tubes using a controlled atmosphere test facility (CATFAC)

    NASA Astrophysics Data System (ADS)

    Martin, Nicholas A.; Helmore, Jonathan J.; White, Samual; Barker Snook, Ieuan L.; Parish, Andy; Gates, Linda S.

    2014-09-01

    We report measurements of the 28 day NO2 diffusive sampling rates for seven designs of Palmes diffusion tubes (PDTs), which were exposed in a controlled atmosphere test facility (CATFAC) containing traceable concentrations of nitrogen dioxide, nitric oxide and water vapour under defined conditions of temperature (20 °C) and wind speed. One of the aims of the work was to implement low cost modifications to the conventional open tube PDT design, using either meshes or filters. This would potentially reduce some of the undesirable bias effects due to wind, which may lead to an over estimation of the NO2 concentration. Exposure tests in the CATFAC were carried out over a wide concentration range applicable to ambient monitoring, and also over a range of wind speeds at a constant concentration. For a given PDT design, the measured NO2 diffusive sampling rates were found to be effectively constant over the conditions tested. These rates were then applied to NO2 field measurements carried out at a monitoring station in central London, and three of the modified PDT designs were found to deliver improved repeatability and consequently reduced measurement uncertainty over the conventional open tubes.

  5. Tropospheric ozone and nitrogen dioxide measurements in urban and rural regions as seen by IASI and GOME-2

    NASA Astrophysics Data System (ADS)

    Safieddine, S.; Clerbaux, C.; George, M.; Hadji-Lazaro, J.; Hurtmans, D.; Coheur, P.-F.; Wespes, C.; Loyola, D.; Valks, P.; Hao, N.

    2013-09-01

    ozone (O3) columns in urban and rural regions as seen by the Infrared Atmospheric Sounding Interferometer (IASI) are analyzed along with the Global Ozone Monitoring Experiment (GOME-2) tropospheric nitrogen dioxide (NO2) columns. Results over nine cities of the Northern Hemisphere for the period 2008-2011 show a typical seasonal behavior of tropospheric O3, with a first maximum reached in late spring because of stratospheric intrusion mainly and a continuous rise till the summer because of the anthropogenic-based ozone production. Over the East Asian cities, a decrease in the O3 tropospheric column is detected during the monsoon period. Seasonal cycling of tropospheric NO2 shows consistent higher values during winter because of the higher anthropogenic sources and longer lifetime. In rural regions, a complex relation between the O3 and NO2 columns is found, with good correlation in summer and winter. O3 concentrations in rural sites are found to be comparable to those closest to the anthropogenic emission sources, with peak values in spring and summer. Furthermore, the effect of the reduction of pollutant emissions in the Beijing region during the Olympic Games of 2008 compared to the same summer period in the following 3 years is studied. GOME-2 NO2 measurements show a reduction up to 54% above Beijing during this period compared to the following 3 years. IASI O3 measurements show an increase of 12% during July 2008 followed by a decrease of 5-6% during the months of August and September.

  6. Nitrogen dioxide and respiratory illness in children. Part I: Health outcomes

    SciTech Connect

    Samet, J.M.; Lambert, W.E.; Skipper, B.J.; Cushing, A.H.; Hunt, W.C.; Young, S.A.; McLaren, L.C.; Schwab, M.; Spengler, J.D. )

    1993-06-01

    We have carried out a prospective cohort study to test the hypothesis that exposure to nitrogen dioxide increases the incidence and severity of respiratory infections during the first 18 months of life. Between January 1988 and June 1990, 1,315 infants were enrolled into the study at birth and followed with prospective surveillance for the occurrence of respiratory infections and monitoring of nitrogen dioxide concentrations in their homes. The subjects were healthy infants from homes without smokers; they were selected with stratification by type of cooking stove at a ratio of four to one for gas and electric stoves. Illness experience was monitored by a daily diary of symptoms completed by the mother and a telephone interview conducted every two weeks. Illnesses with wheezing or wet cough were classified as involving the lower respiratory tract; all other respiratory illnesses were designated as involving the upper respiratory tract. Exposure to nitrogen dioxide was estimated by two-week average concentrations measured in the subjects' bedrooms with passive samplers. This analysis is limited to the 1,205 subjects completing at least one month of observation; of these, 823 completed the full protocol, contributing 82.8% of the total number of days during which the subjects were under observation. Incidence rates for all respiratory illnesses, all upper respiratory illness, all lower respiratory illnesses, and lower respiratory illness further divided into those with any wheezing, or wet cough without wheezing, were examined within strata of nitrogen dioxide exposure at the time of the illness, nitrogen dioxide exposure during the prior month, and type of cooking stove. Consistent trends of increasing illness incidence rates with increasing exposure to nitrogen dioxide were not evident for either the lagged or unlagged exposure variables.

  7. Interaction of glutathione and ascorbic acid in guinea pig lungs exposed to nitrogen dioxide

    SciTech Connect

    Leung, H.-W.; Morrow, P.E.

    1981-01-01

    The interaction of two important water-soluble antioxidants, glutathione and ascorbic acid, was studied. The perfused guinea pig lung was found to contain about twice as much reduced glutathione as ascorbic acid. Nitrogen dioxide exposure decreased the levels of the two antioxidants both in vitro and in vivo. Ascorbic acid concentration was lowered to a greater extent than glutathione. The pulmonary ascorbic acid level was identical in both control and glutathione-deficient guinea pigs exposed to nitrogen dioxide, suggesting that there was little interaction between the two antioxidants in the lungs during oxidant stress.

  8. Validation of OMI Tropospheric Nitrogen Dioxide Column Data Using MAX-DOAS Measurements Deep Inside the North China Plain in June 2006

    NASA Astrophysics Data System (ADS)

    Irie, H.; Kanaya, Y.; Akimoto, H.; Tanimoto, H.; Wang, Z.; Gleason, J. F.; Bucsela, E. J.

    2007-12-01

    A challenge for the quantitative analysis of tropospheric nitrogen dioxide (NO2) column data from satellite observations is likely posed mainly by the lack of satellite-independent observations for validation. We performed such satellite-independent observations of the tropospheric NO2 column using the ground-based Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) technique in the North China Plain (NCP) from 29 May to 29 June, 2006. Comparisons between tropospheric NO2 columns measured by MAX-DOAS and the Ozone Monitoring Instrument (OMI) onboard the Aura satellite indicate that OMI data over NCP likely have a positive bias of 2×1015 molecules cm-2 (~30%), but it is within the estimated random error of 3×1015 molecules cm-2 (~40%). Considering the uncertainty estimated here will pave the way for quantitative studies using the OMI NO2 data over NCP.

  9. Nitrogen oxide abatement by distributed fuel addition. Quarterly report No. 2, November 1, 1987--January 31, 1988

    SciTech Connect

    Wendt, J.O.L.; Meraab, J.

    1988-03-25

    The purpose of this project is to develop techniques for nitrogen oxides abatement by distributed fuel addition. The major nitrogen oxide of interest is Nitric Oxide (NO), a precursor to premature forest damage and to acid rain. Recently interest has also been evoked with respect to an additional oxide of nitrogen, namely Nitrous Oxide (N{sub 2}O). Therefore, abatement measures for NO{sub x} are being investigated to determine their influence on N{sub 2}O as well. This report briefly describes the significance of N{sub 2}O emissions to the environment and the urgent need to develop techniques that can reduce emissions of both NO and N{sub 2}O. Reburning through distributed fuel addition may be an effective technique for NO{sub x} (mainly NO) emission control as described in the previous quarterly report. Reburning may also be effective in reducing N{sub 2}O levels. A technique for N{sub 2}O measurement by gas chromatography/electron capture detection was developed during this quarter, and is described in this report. This analysis technique will be used in the proposed experimental study to investigate the effectiveness of reburning on N{sub 2}O control.

  10. Long-term effects of ozone and nitrogen dioxide on the metabolism and population of alveolar macrophages

    SciTech Connect

    Mochitate, K.; Ishida, K.; Ohsumi, T.; Miura, T. )

    1992-04-01

    To investigate how alveolar macrophages adapt themselves to oxidative pollutants in the long term, rats were exposed to a strong oxidant, ozone (O3), or a weak oxidant, nitrogen dioxide (NO2), for a maximum duration of 12 wk. After exposures, alveolar macrophages were collected by pulmonary lavage. Throughout 11 wk of exposure to 0.2 ppm O3, the specific activities of glucose-6-phosphate dehydrogenase (G6PDH) and glutathione peroxidase of the peroxidative metabolic pathway and pyruvate kinase and hexokinase of the glycolytic pathway were 40-70% elevated over the controls in alveolar macrophages. The population of alveolar macrophages was consistently 60% higher than the controls. The small-sized macrophages, immature macrophages, preferentially increased. To the contrary, the thymidine incorporation per cell was always 20-30% lower than in the controls, although the total incorporation remained unchanged. No infiltration of polymorphonuclear leukocytes occurred. By 12 wk of exposures to 1.2 and 4.0 ppm NO2, the population of alveolar macrophages increased 30% over the control. Among the enzymes examined, however, only the G6PDH activity increased 10% for 4.0 ppm NO2. No increase in the enzyme activities occurred for 1.2 ppm NO2. Based on these results, alveolar macrophages adapt themselves to the long-term exposure of O3 or NO2 by recruiting immature macrophages through an apparent influx of monocytes. During the exposure to O3, the peroxidative metabolic and glycolytic pathways are enhanced persistently in alveolar macrophages, whereas both pathways were not enhanced by the exposures to NO2.