Ozone Production Using Pulsed Dielectric Barrier Discharge in Oxygen

OpenAIRE

Samaranayake, W. J. M.; Miyahara, Y.; Namihira, T.; Katsuki, S.; Hackam, R.; Akiyama, H.; ナミヒラ, タカオ; カツキ, スナオ; アキヤマ, ヒデノリ; 浪平, 隆男; 勝木, 淳; 秋山, 秀典

2000-01-01

The production of ozone was investigated using a dielectric barrier discharge in oxygen, and employing short-duration pulsed power. The dependence of the ozone concentration (parts per million, ppm) and ozone production yield (g(O3)/kWh) on the peak pulsed voltage (17.5 to 57.9 kV) and the pulse repetition rate (25 to 400 pulses/s, pps) were investigated. In the present study, the following parameters were kept constant: a pressure of 1.01×105 Pa, a temperature of 26±4°C a gas flow rate of 3....

Ozone induced leaf loss and decreased leaf production of European Holly (Ilex aquifolium L.) over multiple seasons

International Nuclear Information System (INIS)

Ranford, Jonathan; Reiling, Kevin

2007-01-01

European Holly (Ilex aquifolium L.) was used to study the impact of one short (28 day) ozone fumigation episode on leaf production, leaf loss and stomatal conductance (g s ), in order to explore potential longer term effects over 3 growing seasons. Young I. aquifolium plants received an episode of either charcoal-filtered air or charcoal-filtered air with 70 nl l -1 O 3 added for 7 h d -1 over a 28 day period from June 15th 1996, then placed into ambient environment, Stoke-on-Trent, U.K. Data were collected per leaf cohort over the next three growing seasons. Ozone exposure significantly increased leaf loss and stomatal conductance and reduced leaf production over all subsequent seasons. Impact of the initial ozone stress was still detected in leaves that had no direct experimental ozone exposure. This study has shown the potential of ozone to introduce long-term phenological perturbations into ecosystems by influencing productivity over a number of seasons. - Ozone significantly alters Ilex aquifolium leaf production and loss over multiple seasons

Exploring the roles of temperature and NOx on ozone production in the Sacramento urban plume

Science.gov (United States)

Lafranchi, B. W.; Cohen, R. C.

2009-12-01

We investigate the role of temperature and NOx (NOx = NO+NO2) on ozone (O3) production in the Sacramento urban plume over a stretch of seven years (2001-2007) using data collected at UC Blodgett Forest Research Station (a forested site in the Sierra Nevadas about 80 km downwind of Sacramento, CA) and at a series of California Air Resources Board (CARB) sites along the Sacramento-Blodgett transect. The consistent daytime wind patterns between the Central Valley of California and the foothills of the Sierra Nevada mountains permits the assumption of plume transport from downtown Sacramento, over the CARB monitoring sites in the eastern suburbs, and past the Blodgett Forest research site. While NOx emissions are limited primarily to the urban and suburban regions of the transect, biogenic volatile organic compound (VOC) emissions are significant throughout the transect, thus there is a fast transition from VOC-limited to NOx-limited as the plume travels away from the urban center, and we have the opportunity to analyze the differences in ozone production across these two chemical regimes. For this analysis, the Sacramento-Blodgett transect is separated into three segments: urban, suburban, and rural, defined by the locations of selected monitoring sites. Ozone concentrations across each segment are controlled by chemical production (Pchem) and loss (Lchem), deposition to surfaces (Ldep), and mixing with background air (Lmix). At an assumed deposition rate, mixing rate, and background O3 concentration, the net chemical flux of ozone (Pchem - Lchem) can be inferred from differences in ozone concentrations between adjacent monitoring sites. We show that ozone production rates, in general, increase with temperature. We also show that decreases in NOx emissions over the period from 2001-2007 have been effective at reducing ozone production at all points along the transect, but only on days where temperatures are highest. At low temperatures, this decrease is less apparent

Ozone production process in pulsed positive dielectric barrier discharge

Science.gov (United States)

Ono, Ryo; Oda, Tetsuji

2007-01-01

The ozone production process in a pulsed positive dielectric barrier discharge (DBD) is studied by measuring the spatial distribution of ozone density using a two-dimensional laser absorption method. DBD occurs in a 6 mm point-to-plane gap with a 1 mm-thick glass plate placed on the plane electrode. First, the propagation of DBD is observed using a short-gated ICCD camera. It is shown that DBD develops in three phases: primary streamer, secondary streamer and surface discharge phases. Next, the spatial distribution of ozone density is measured. It is shown that ozone is mostly produced in the secondary streamer and surface discharge, while only a small amount of ozone is produced in the primary streamer. The rate coefficient of the ozone production reaction, O + O2 + M → O3 + M, is estimated to be 2.5 × 10-34 cm6 s-1.

Ozone production process in pulsed positive dielectric barrier discharge

International Nuclear Information System (INIS)

Ono, Ryo; Oda, Tetsuji

2007-01-01

The ozone production process in a pulsed positive dielectric barrier discharge (DBD) is studied by measuring the spatial distribution of ozone density using a two-dimensional laser absorption method. DBD occurs in a 6 mm point-to-plane gap with a 1 mm-thick glass plate placed on the plane electrode. First, the propagation of DBD is observed using a short-gated ICCD camera. It is shown that DBD develops in three phases: primary streamer, secondary streamer and surface discharge phases. Next, the spatial distribution of ozone density is measured. It is shown that ozone is mostly produced in the secondary streamer and surface discharge, while only a small amount of ozone is produced in the primary streamer. The rate coefficient of the ozone production reaction, O + O 2 + M → O 3 + M, is estimated to be 2.5 x 10 -34 cm 6 s -1

Ozone's impact on public health: Contributions from indoor exposures to ozone and products of ozone-initiated chemistry

DEFF Research Database (Denmark)

Weschler, Charles J.

2006-01-01

OBJECTIVES: The associations between ozone concentrations measured outdoors and both morbidity and mortality may be partially due to indoor exposures to ozone and ozone-initiated oxidation products. In this article I examine the contributions of such indoor exposures to overall ozone-related heal...

Ozone production process in pulsed positive dielectric barrier discharge

Energy Technology Data Exchange (ETDEWEB)

Ono, Ryo [High Temperature Plasma Center, University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa, Chiba, 227-8568 (Japan); Oda, Tetsuji [Department of Electrical Engineering, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8656 (Japan)

2007-01-07

The ozone production process in a pulsed positive dielectric barrier discharge (DBD) is studied by measuring the spatial distribution of ozone density using a two-dimensional laser absorption method. DBD occurs in a 6 mm point-to-plane gap with a 1 mm-thick glass plate placed on the plane electrode. First, the propagation of DBD is observed using a short-gated ICCD camera. It is shown that DBD develops in three phases: primary streamer, secondary streamer and surface discharge phases. Next, the spatial distribution of ozone density is measured. It is shown that ozone is mostly produced in the secondary streamer and surface discharge, while only a small amount of ozone is produced in the primary streamer. The rate coefficient of the ozone production reaction, O + O{sub 2} + M {yields} O{sub 3} + M, is estimated to be 2.5 x 10{sup -34} cm{sup 6} s{sup -1}.

Quantifying Ozone Production throughout the Boundary Layer from High Frequency Tethered Profile Measurements during a High Ozone Episode in the Uinta Basin, Utah

Science.gov (United States)

Sterling, C. W.; Johnson, B.; Schnell, R. C.; Oltmans, S. J.; Cullis, P.; Hall, E. G.; Jordan, A. F.; Windell, J.; McClure-Begley, A.; Helmig, D.; Petron, G.

2015-12-01

During the Uinta Basin Winter Ozone Study (UBWOS) in Jan - Feb 2013, 735 tethered ozonesonde profiles were obtained at 3 sites including during high wintertime photochemical ozone production events that regularly exceeded 125 ppb. High resolution profiles of ozone and temperature with altitude, measured during daylight hours, showed the development of approximately week long high ozone episodes building from background levels of ~40 ppb to >150 ppb. The topography of the basin combined with a strong temperature inversion trapped oil and gas production effluents in the basin and the snow covered surface amplified the sun's radiation driving the photochemical ozone production at rates up to 13 ppb/hour in a cold layer capped at 1600-1700 meters above sea level. Beginning in mid-morning, ozone mixing ratios throughout the cold layer increased until late afternoon. Ozone mixing ratios were generally constant with height indicating that ozone production was nearly uniform throughout the depth of the cold pool. Although there was strong diurnal variation, ozone mixing ratios increased during the day more than decreased during the night, resulting in elevated levels the next morning; an indication that nighttime loss processes did not compensate for daytime production. Even though the 3 tethersonde sites were at elevations differing by as much as 140 m, the top of the high ozone layer was nearly uniform in altitude at the 3 locations. Mobile van surface ozone measurements across the basin confirmed this capped structure of the ozone layer; the vehicle drove out of high ozone mixing ratios at an elevation of ~1900 meters above sea level, above which free tropospheric ozone mixing ratios of ~50 ppb were measured. Exhaust plumes from a coal-fired power plant in the eastern portion of the basin were intercepted by the tethersondes. The structure of the profiles clearly showed that effluents in the plumes were not mixed downward and thus did not contribute precursor nitrogen

Efficiency of ozone production by pulsed positive corona discharge in synthetic air

Energy Technology Data Exchange (ETDEWEB)

Simek, Milan [Institute of Plasma Physics, Department of Pulsed Plasma Systems, Academy of Sciences of the Czech Republic, Prague (Czech Republic)]. E-mail: simek@ipp.cas.cz; Clupek, Martin [Institute of Plasma Physics, Department of Pulsed Plasma Systems, Academy of Sciences of the Czech Republic, Prague (Czech Republic)

2002-06-07

We have studied the efficiency of ozone production by pulsed positive corona discharge in coaxial wire-cylinder geometry at atmospheric pressure. A corona discharge was generated by short ({approx}150 ns) high voltage pulses applied between a silver coated copper wire anode and stainless steel cylinder cathode in synthetic air. A pyrex probe and Teflon tube was used for collecting discharge products and an ozone concentration was monitored outside of the discharge chamber by a non-dispersive UV absorption technique. The production of ozone was investigated as a function of energy density (10{sup -4}-3x10{sup -1} Wh l{sup -1}) delivered to the discharge volume by combining the discharge frequency (0.1-10 Hz) and airflow rate (1-32 l min{sup -1}). From ozone concentration measurements we have evaluated the ozone production, yield and production energy cost. The ozone production yield and cost vary in the range of 15-55 g kWh{sup -1} and 35-110 eV/molecule. (author)

Ozone production at the National Synchrotron Light Source

International Nuclear Information System (INIS)

Weilandics, C.; Rohrig, N.; Gmur, N.F.

1987-01-01

Ozone production by synchrotron radiation as a function of power density in air was investigated using a white beam at the BNL National Synchrotron Light Source (NSLS) x-ray ring. Power densities were calculated from the energy spectrum at 2.52 GeV. Ozone concentrations in small beam pipes were measured for power densities between I = 10 12 and 10 15 eV . cm -3 . sec -1 . The measured ozone half-life was 37 +- 2 min. The measured G-value was 2.69 +- 0.14 mol/100 eV and the ozone destruction factor k was less than 7 x 10 -19 cm 3 . eV -1 . The random uncertainties stated are approximately one standard error. The large departure of the values for G and k from previous values suggest that some undiscovered systematic error may exist in the experiment. Ozone concentration in excess of the 0.1 ppM ACGIH TLV can be generated in the experimental hutches but can readily be controlled. Industrial hygiene aspects of operation and possible control measures will be discussed. 19 refs., 7 figs., 3 tabs

DC corona discharge ozone production enhanced by magnetic field

Science.gov (United States)

Pekárek, S.

2010-01-01

We have studied the effect of a stationary magnetic field on the production of ozone from air at atmospheric pressure by a negative corona discharge in a cylindrical electrode configuration. We used a stainless steel hollow needle placed at the axis of the cylindrical discharge chamber as a cathode. The outer wall of the cylinder was used as an anode. The vector of magnetic induction was perpendicular to the vector of current density. We found that: (a) the magnetic field extends the current voltage range of the discharge; (b) for the discharge in the Trichel pulses regime and in the pulseless glow regime, the magnetic field has no substantial effect on the discharge voltage or on the concentration of ozone that is produced; (c) for the discharge in the filamentary streamer regime for a particular current, the magnetic field increases the discharge voltage and consequently an approximately 30% higher ozone concentration can be obtained; (d) the magnetic field does not substantially increase the maximum ozone production yield. A major advantage of using a magnetic field is that the increase in ozone concentration produced by the discharge can be obtained without additional energy requirements.

Products and kinetics of the heterogeneous reaction of suspended vinclozolin particles with ozone.

Science.gov (United States)

Gan, Jie; Yang, Bo; Zhang, Yang; Shu, Xi; Liu, Changgeng; Shu, Jinian

2010-11-25

Vinclozolin is a widely used fungicide that can be released into the atmosphere via application and volatilization. This paper reports an experimental investigation on the heterogeneous ozonation of vinclozolin particles. The ozonation of vinclozolin adsorbed on azelaic acid particles under pseudo-first-order conditions is investigated online with a vacuum ultraviolet photoionization aerosol time-of-flight mass spectrometer (VUV-ATOFMS). The ozonation products are analyzed with a combination of VUV-ATOFMS and GC/MS. Two main ozonation products are observed. The formation of the ozonation products results from addition of O(3) on the C-C double bond of the vinyl group. The heterogeneous reactive rate constant of vinclozolin particles under room temperature is (2.4 ± 0.4) × 10(-17) cm(3) molecules(-1) s(-1), with a corresponding lifetime at 100 ppbv O(3) of 4.3 ± 0.7 h, which is almost comparable with the estimated lifetime due to the reaction with atmospheric OH radicals (∼1.7 h). The reactive uptake coefficient for O(3) on vinclozolin particles is (6.1 ± 1.0) × 10(-4).

Southern Hemisphere Additional Ozonesondes (SHADOZ) Ozone Climatology (2005-2009): Tropospheric and Tropical Tropopause Layer (TTL) Profiles with Comparisons to Omi-based Ozone Products

Science.gov (United States)

Thompson, Anne M.; Miller, Sonya K.; Tilmes, Simone; Kollonige, Debra W.; Witte, Jacquelyn C.; Oltmans, Samuel J.; Johnson, Brian J.; Fujiwara, Masatomo; Schmidlin, F. J.; Coetzee, G. J. R.;

The Transition of Atmospheric Infrared Sounder Total Ozone Products to Operations

Science.gov (United States)

Berndt, Emily; Zavodsky, Bradley; Jedlovec, Gary

2014-01-01

The National Aeronautics and Space Administration Short-term Prediction Research and Transition Center (NASA SPoRT) has transitioned a total column ozone product from the Atmospheric Infrared Sounder (AIRS) retrievals to the Weather Prediction Center and Ocean Prediction Center. The total column ozone product is used to diagnose regions of warm, dry, ozone-rich, stratospheric air capable of descending to the surface to create high-impact non-convective winds. Over the past year, forecasters have analyzed the Red, Green, Blue (RGB) Air Mass imagery in conjunction with the AIRS total column ozone to aid high wind forecasts. One of the limitations of the total ozone product is that it is difficult for forecasters to determine whether elevated ozone concentrations are related to stratospheric air or climatologically high values of ozone in certain regions. During the summer of 2013, SPoRT created an AIRS ozone anomaly product which calculates the percent of normal ozone based on a global stratospheric ozone mean climatology. With the knowledge that ozone values 125 percent of normal and greater typically represent stratospheric air; the anomaly product can be used with the total column ozone product to confirm regions of stratospheric air. This paper describes the generation of these products along with forecaster feedback concerning the use of the AIRS ozone products in conjunction with the RGB Air Mass product to access the utility and transition of the products.

Characterization of surface dielectric barrier discharge influenced by intermediate frequency for ozone production

Science.gov (United States)

Abdelaziz, Ayman A.; Ishijima, Tatsuo; Seto, Takafumi; Osawa, Naoki; Wedaa, Hassan; Otani, Yoshio

2016-06-01

The aim of this study is to investigate the effect of the intermediate frequency (1-10 kHz) of the sinusoidal driving voltage on the characteristics of a developed surface dielectric barrier discharge (SDBD)-based reactor having spikes on its discharge electrode. Moreover, its influence on the production of ozone and nitrogen oxide byproducts is evaluated. The results show that SDBD is operated in the filamentary mode at all the frequencies. Nevertheless, the pulses of the discharge current at high frequencies are much denser and have higher amplitudes than those at low frequencies. The analysis of the power consumed in the reactor shows that a small portion of the input power is dissipated in the dielectric material of SDBD source, whereas the major part of the power is consumed in the plasma discharge. The results of the ozone production show that higher frequencies have a slightly adverse effect on the ozone production at relatively high energy density values, where the ozone concentration is slightly decreased when the frequency is increased at the same energy density. The temperature of the discharge channels and gas is not a crucial factor for the decomposition of ozone in this reactor, while the results of the measurements of nitrogen oxides characteristics indicate that the formation of NO and NO2 has a significant adverse effect on the production efficiency of ozone due to their oxidation to another nitrogen oxides and their catalytic effect.

Characterization of surface dielectric barrier discharge influenced by intermediate frequency for ozone production

International Nuclear Information System (INIS)

Abdelaziz, Ayman A; Ishijima, Tatsuo; Seto, Takafumi; Otani, Yoshio; Osawa, Naoki; Wedaa, Hassan

2016-01-01

The aim of this study is to investigate the effect of the intermediate frequency (1–10 kHz) of the sinusoidal driving voltage on the characteristics of a developed surface dielectric barrier discharge (SDBD)-based reactor having spikes on its discharge electrode. Moreover, its influence on the production of ozone and nitrogen oxide byproducts is evaluated. The results show that SDBD is operated in the filamentary mode at all the frequencies. Nevertheless, the pulses of the discharge current at high frequencies are much denser and have higher amplitudes than those at low frequencies. The analysis of the power consumed in the reactor shows that a small portion of the input power is dissipated in the dielectric material of SDBD source, whereas the major part of the power is consumed in the plasma discharge. The results of the ozone production show that higher frequencies have a slightly adverse effect on the ozone production at relatively high energy density values, where the ozone concentration is slightly decreased when the frequency is increased at the same energy density. The temperature of the discharge channels and gas is not a crucial factor for the decomposition of ozone in this reactor, while the results of the measurements of nitrogen oxides characteristics indicate that the formation of NO and NO 2 has a significant adverse effect on the production efficiency of ozone due to their oxidation to another nitrogen oxides and their catalytic effect. (paper)

Production of ozone using nanosecond short pulsed power

OpenAIRE

Shimomura, N.; Wakimoto, M.; Togo, H.; Namihira, Takao; Akiyama, Hidenori; ナミヒラ, タカオ; アキヤマ, ヒデノリ; 浪平, 隆男; 秋山, 秀典

2003-01-01

Production of ozone is one of the most typical industrial and commercial applications of electrical discharge. The demand of ozone will be increasing for wholesome and environment-friendly sterilizations. The production of ozone using the pulsed power discharge will apply electron accelerations around the head of streamer discharge. The breakdowns in reactor, however, often limit the efficient production. The pulse shape should be controlled for dimension of the reactor. On the other hand, th...

Effect of fiber material on ozone removal and carbonyl production from carpets

Science.gov (United States)

Abbass, Omed A.; Sailor, David J.; Gall, Elliott T.

2017-01-01

Indoor air quality is affected by indoor materials such as carpets that may act as sources and/or sinks of gas-phase air pollutants. Heterogeneous reactions of ozone with carpets may result in potentially harmful products. In this study, indoor residential carpets of varying fiber types were tested to evaluate their ability to remove ozone, and to assess their role in the production of carbonyls when exposed to elevated levels of ozone. Tests were conducted with six types of new unused carpets. Two sets of experiments were conducted, the first measured ozone removal and ozone deposition velocities, and the second measured primary carbonyl production and secondary production as a result of exposure to ozone. The tests were conducted using glass chambers with volume of 52 L each. Air exchange rates for all tests were 3 h-1. The ozone removal tests show that, for the conditions tested, the polyester carpet sample had the lowest ozone removal (40%), while wool carpet had the greatest ozone removal (65%). Most carpet samples showed higher secondary than primary carbonyl emissions, with carpets containing polypropylene fibers being a notable exception. Carpets with polyester fibers had both the highest primary and secondary emissions of formaldehyde among all samples tested. While it is difficult to make blanket conclusions about the relative air quality merits of various carpet fiber options, it is clear that ozone removal percentages and emissions of volatile organic compounds can vary drastically as a function of fiber type.

Emissions lifetimes and ozone formation in power plant plumes

Energy Technology Data Exchange (ETDEWEB)

Ryerson, T.B.; Buhr, M.P.; Frost, G.J.; Goldan, P.D.; Holloway, J.S.; Huebler, G.; Jobson, B.T.; Kuster, W.C.; McKeen, S.A.; Parrish, D.D.; Roberts, J.M.; Sueper, D.T.; Trainer, M.; Williams, J.; Fehsenfeld, F.C. [NOAA Aeronomy Laboratory, Boulder, CO (United States)

1998-09-20

The concept of ozone production efficiency (OPE) per unit NO{sub x} is based on photochemical models and provides a tool with which to assess potential regional tropospheric ozone control strategies involving NO{sub x} emissions reductions. An aircraft study provided data from which power plant emissions removal rates and measurement-based estimates of OPE are estimated. This study was performed as part of the Southern Oxidants Study - 1995 Nashville intensive and focuses on the evolution of NO{sub x}, SO{sub 2}, and ozone concentrations in coal-fired power plant plumes during transport. Two approaches are examined. A mass balance approach accounts for mixing effects within the boundary layer and is used to calculate effective boundary layer removal rates for NO{sub x} and SO{sub 2} and to estimate net OPE, Net OPE is more directly comparable to photochemical model results than previous measurement-based estimates. Derived net production efficiencies from mass balance range from 1 to 3 molecules of ozone produced per molecule of NO{sub x} emitted. A concentration ratio approach provides an estimate of removal rates of primary emissions relative to a tracer species. This approach can be combined with emissions ratio information to provide upper limit estimates of OPE that range from 2 to 7. Both approaches illustrate the dependence of ozone production on NO{sub x} source strength in these large point source plumes. The dependence of total ozone production, ozone production efficiency, and the rate of ozone production on NO{sub x} source strength is examined. These results are interpreted in light of potential ozone control strategies for the region. 42 refs., 8 figs., 5 tabs.

Emissions lifetimes and ozone formation in power plant plumes

International Nuclear Information System (INIS)

Ryerson, T.B.; Buhr, M.P.; Frost, G.J.; Goldan, P.D.; Holloway, J.S.; Huebler, G.; Jobson, B.T.; Kuster, W.C.; McKeen, S.A.; Parrish, D.D.; Roberts, J.M.; Sueper, D.T.; Trainer, M.; Williams, J.; Fehsenfeld, F.C.

1998-01-01

The concept of ozone production efficiency (OPE) per unit NO x is based on photochemical models and provides a tool with which to assess potential regional tropospheric ozone control strategies involving NO x emissions reductions. An aircraft study provided data from which power plant emissions removal rates and measurement-based estimates of OPE are estimated. This study was performed as part of the Southern Oxidants Study - 1995 Nashville intensive and focuses on the evolution of NO x , SO 2 , and ozone concentrations in coal-fired power plant plumes during transport. Two approaches are examined. A mass balance approach accounts for mixing effects within the boundary layer and is used to calculate effective boundary layer removal rates for NO x and SO 2 and to estimate net OPE, Net OPE is more directly comparable to photochemical model results than previous measurement-based estimates. Derived net production efficiencies from mass balance range from 1 to 3 molecules of ozone produced per molecule of NO x emitted. A concentration ratio approach provides an estimate of removal rates of primary emissions relative to a tracer species. This approach can be combined with emissions ratio information to provide upper limit estimates of OPE that range from 2 to 7. Both approaches illustrate the dependence of ozone production on NO x source strength in these large point source plumes. The dependence of total ozone production, ozone production efficiency, and the rate of ozone production on NO x source strength is examined. These results are interpreted in light of potential ozone control strategies for the region. 42 refs., 8 figs., 5 tabs

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

Science.gov (United States)

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

Experimental effect of ozone upon the microbial flora of commercially produced dairy fermented products.

Science.gov (United States)

Alexopoulos, A; Plessas, S; Kourkoutas, Y; Stefanis, C; Vavias, S; Voidarou, C; Mantzourani, I; Bezirtzoglou, E

2017-04-04

Ozone was used to control spoilage microorganisms during the manufacturing of dairy products. Ozone stream was applied onto the surface of freshly filled yoghurt cups just before storage for curd development in order to prevent cross contamination from spoilage airborne microorganisms. Accordingly, brine solution was bubbled with ozone for various periods of time and used for ripening of white (feta type) cheese. Both products were subjected to a continuous monitoring of microbial load and also tested for their sensorial properties. In ozonated yoghurt samples there was a reduction in mould counts of approximately 0.6Logcfu/g (25.1%) by the end of the monitoring period in relation to the control samples. In white cheese ripened with ozonated brine (1.3mg/L O 3 , NaCl 5%) it seems that ozone treatment during the two months of observation reduced some of the mould load but without offering any advantages over the use of traditional brine (NaCl 7%). However, some sensorial alterations were observed, probably due to the organic load in the brine which deactivates ozone in early stages of application. It is concluded that, if the factors of time and concentration of ozone are configured properly, ozonation could be a promising approach safeguarding the production of some dairy products. Copyright © 2017 Elsevier B.V. All rights reserved.

Drift-corrected Odin-OSIRIS ozone product: algorithm and updated stratospheric ozone trends

Directory of Open Access Journals (Sweden)

A. E. Bourassa

2018-01-01

Full Text Available A small long-term drift in the Optical Spectrograph and Infrared Imager System (OSIRIS stratospheric ozone product, manifested mostly since 2012, is quantified and attributed to a changing bias in the limb pointing knowledge of the instrument. A correction to this pointing drift using a predictable shape in the measured limb radiance profile is implemented and applied within the OSIRIS retrieval algorithm. This new data product, version 5.10, displays substantially better both long- and short-term agreement with Microwave Limb Sounder (MLS ozone throughout the stratosphere due to the pointing correction. Previously reported stratospheric ozone trends over the time period 1984–2013, which were derived by merging the altitude–number density ozone profile measurements from the Stratospheric Aerosol and Gas Experiment (SAGE II satellite instrument (1984–2005 and from OSIRIS (2002–2013, are recalculated using the new OSIRIS version 5.10 product and extended to 2017. These results still show statistically significant positive trends throughout the upper stratosphere since 1997, but at weaker levels that are more closely in line with estimates from other data records.

Effect of voltage waveform on dielectric barrier discharge ozone production efficiency

Science.gov (United States)

Mericam-Bourdet, N.; Kirkpatrick, M. J.; Tuvache, F.; Frochot, D.; Odic, E.

2012-03-01

Dielectric barrier discharges (DBDs) are commonly used for gas effluent cleanup and ozone generation. For these applications, the energy efficiency of the discharge is a major concern. This paper reports on investigations carried out on the voltage shape applied to DBD reactor electrodes, aiming to evaluate a possible energy efficiency improvement for ozone production. Two DBD reactor geometries were used: pin-to-pin and cylinder-to-cylinder, both driven either by a bi-directional power supply (voltage rise rate 1 kV/μs) or by a pulsed power supply (voltage rise rate 1 kV/ns). Ozone formed in dry air was measured at the reactor outlet. Special attention was paid to discharge input power evaluation using different methods including instantaneous current-voltage product and transferred charge-applied voltage figures. The charge transferred by the discharges was also correlated to the ozone production. It is shown that, in the case of the DBD reactors under investigation, the applied voltage shape has no influence on the ozone production efficiency. For the considered voltage rise rate, the charge deposit on the dielectric inserted inside the discharge gap is the important factor (as opposed to the voltage shape) governing the efficiency of the discharge - it does this by tailoring the duration of the current peak into the tens of nanosecond range.

Levofloxacin oxidation by ozone and hydroxyl radicals: kinetic study, transformation products and toxicity.

Science.gov (United States)

Hamdi El Najjar, Nasma; Touffet, Arnaud; Deborde, Marie; Journel, Romain; Leitner, Nathalie Karpel Vel

2013-10-01

This work was carried out to investigate the fate of the antibiotic levofloxacin upon oxidation with ozone and hydroxyl radicals. A kinetic study was conducted at 20 °C for each oxidant. Ozonation experiments were performed using a competitive kinetic method with carbamazepin as competitor. Significant levofloxacin removal was observed during ozonation and a rate constant value of 6.0×10(4) M(-1) s(-1) was obtained at pH 7.2. An H2O2/UV system was used for the formation of hydroxyl radicals HO. The rate constant of HO was determined in the presence of a high H2O2 concentration. The kinetic expressions yielded a [Formula: see text] value of 4.5×10(9) M(-1) s(-1) at pH 6.0 and 5.2×10(9) M(-1) s(-1) at pH 7.2. These results were used to develop a model to predict the efficacy of the ozonation process and pharmaceutical removal was estimated under different ozonation conditions (i.e. oxidant concentrations and contact times). The results showed that levofloxacin was completely degraded by molecular ozone during ozonation of water and that hydroxyl radicals had no effect in real waters conditions. Moreover, LC/MS/MS and toxicity assays using Lumistox test were performed to identify ozonation transformation products. Under these conditions, four transformation products were observed and their chemical structures were proposed. The results showed an increase in toxicity during ozonation, even after degradation of all of the observed transformation products. The formation of other transformation products not identified under our experimental conditions could be responsible for the observed toxicity. These products might be ozone-resistant and more toxic to Vibrio fisheri than levofloxacin. Copyright © 2013 Elsevier Ltd. All rights reserved.

Ozone production by corona discharges during a convective event in DISCOVER-AQ Houston

Science.gov (United States)

Kotsakis, Alexander; Morris, Gary A.; Lefer, Barry; Jeon, Wonbae; Roy, Anirban; Minschwaner, Ken; Thompson, Anne M.; Choi, Yunsoo

2017-07-01

An ozonesonde launched near electrically active convection in Houston, TX on 5 September 2013 during the NASA DISCOVER-AQ project measured a large enhancement of ozone throughout the troposphere. A separate ozonesonde was launched from Smith Point, TX (∼58 km southeast of the Houston site) at approximately the same time as the launch from Houston and did not measure that enhancement. Furthermore, ozone profiles for the descent of both sondes agreed well with the ascending Smith Point profile, suggesting a highly localized event in both space and time in which an anomalously large enhancement of 70-100 ppbv appeared in the ascending Houston ozonesonde data. Compared to literature values, such an enhancement appears to be the largest observed to date. Potential sources of the localized ozone enhancement such as entrainment of urban or biomass burning emissions, downward transport from the stratosphere, photochemical production from lightning NOx, and direct ozone production from corona discharges were investigated using model simulations. We conclude that the most likely explanation for the large ozone enhancement is direct ozone production by corona discharges. Integrating the enhancement seen in the Houston ozone profile and using the number of electrical discharges detected by the NLDN (or HLMA), we estimate a production of 2.48 × 1028 molecules of ozone per flash which falls within the range of previously recorded values (9.89 × 1026-9.82 × 1028 molecules of ozone per flash). Since there is currently no parameterization for the direct production of ozone from corona discharges we propose the implementation of an equation into a chemical transport model. Ultimately, additional work is needed to further understand the occurrence and impact of corona discharges on tropospheric chemistry on short and long timescales.

Photochemical processes and ozone production in Finnish conditions

Energy Technology Data Exchange (ETDEWEB)

Laurila, T; Hakola, H [Finnish Meteorological Inst., Helsinki (Finland). Air Quality Dept.

1997-12-31

Photochemical ozone production is observed in March-September. Highest ozone concentrations and production efficiencies are observed in spring in the northern parts and in summer in the southern parts of the country. VOC concentrations are relatively low compared to continental areas in general. During the growing season a substantial part of the total reactive mass of VOCs is of biogenic origin. Large forest areas absorb ozone substantially, decreasing the ambient ozone concentrations in central and northern parts of Finland where long-range transport of ozone is relatively important compared to local production. The aim of the work conducted at Finnish Meteorological Institute has been to characterise concentrations of photochemically active species in the boundary layer and their photochemical formation and deposition including the effects on vegetation. Also interactions between the boundary layer and free troposphere of ozone have been studied. In the future, fluxes of both biogenic species and air pollutants will be measured and the models will be further developed so that the photochemical and micrometeorological processes could be better understood

Photochemical processes and ozone production in Finnish conditions

Energy Technology Data Exchange (ETDEWEB)

Laurila, T.; Hakola, H. [Finnish Meteorological Inst., Helsinki (Finland). Air Quality Dept.

1996-12-31

Photochemical ozone production is observed in March-September. Highest ozone concentrations and production efficiencies are observed in spring in the northern parts and in summer in the southern parts of the country. VOC concentrations are relatively low compared to continental areas in general. During the growing season a substantial part of the total reactive mass of VOCs is of biogenic origin. Large forest areas absorb ozone substantially, decreasing the ambient ozone concentrations in central and northern parts of Finland where long-range transport of ozone is relatively important compared to local production. The aim of the work conducted at Finnish Meteorological Institute has been to characterise concentrations of photochemically active species in the boundary layer and their photochemical formation and deposition including the effects on vegetation. Also interactions between the boundary layer and free troposphere of ozone have been studied. In the future, fluxes of both biogenic species and air pollutants will be measured and the models will be further developed so that the photochemical and micrometeorological processes could be better understood

The gas phase reaction of ozone with 1,3-butadiene: formation yields of some toxic products

Science.gov (United States)

Kramp, Franz; Paulson, Suzanne E.

The formation yields of acrolein, 1,2-epoxy-3-butene and OH radicals have been measured from reaction of ozone with 1,3-butadiene at room temperature and atmosphere pressure. 1,3,5-Trimethyl benzene was added to scavenge OH radicals in measurements of product yields. In separate experiments, small quantities of 1,3,5-trimethyl benzene were added as a tracer for OH. Formation yields of acrolein of (52±7)%, 1,2-epoxy-3-butene of (3.1±0.5)% and OH radicals of (13±3)% were observed. In addition, the rate coefficient of the gas-phase reaction of ozone with 1,2-epoxy-3-butene was measured both directly and relative to propene, finding an average of (1.6±0.4)×10 -18 cm 3 molecule -1 s -1, respectively, at 296±2 K. The results are briefly discussed in terms of the effect of atmospheric processing on the toxicity of 1,3-butadiene.

Ozone and hydrogen peroxide applications for disinfection by-products control in drinking water

International Nuclear Information System (INIS)

Collivignarelli, C.; Sorlini, S.; Riganti, V.

2001-01-01

A great interest has been developed during the last years for ozone in drinking water treatments thanks to its strong oxidant and disinfectant power and for its efficiency in disinfection by-products (DBPs) precursors removal. However ozonization produces some specific DBPs, such as aldehydes and ketones; moreover, the presence of bromide in raw water engages ozone in a complex cycle in which both organic bromide and inorganic bromate are end products. In this paper the combination of hydrogen peroxide with ozone (known as peroxone process) and the ozone alone process were experimented on one surface water coming from the lake of Brugneto (Genova) in order to investigate bromate formation and trihalomethanes precursors removal during the oxidation process. The results show that the advanced peroxone process can be applied for bromate reduction (about 30-40%) with better results in comparison with the ozone alone process, while no advantages are shown for THMs precursors removal. The addition of in-line filtration step after pre-oxidation improves both bromate and THMs precursors removal, particularly with increasing hydrogen peroxide/ozone ratio in the oxidation step [it

Observations of the vertical distributions of summertime atmospheric pollutants and the corresponding ozone production in Shanghai, China

Science.gov (United States)

Xing, Chengzhi; Liu, Cheng; Wang, Shanshan; Chan, Ka Lok; Gao, Yang; Huang, Xin; Su, Wenjing; Zhang, Chengxin; Dong, Yunsheng; Fan, Guangqiang; Zhang, Tianshu; Chen, Zhenyi; Hu, Qihou; Su, Hang; Xie, Zhouqing; Liu, Jianguo

2017-12-01

Ground-based multi-axis differential optical absorption spectroscopy (MAX-DOAS) and lidar measurements were performed in Shanghai, China, during May 2016 to investigate the vertical distribution of summertime atmospheric pollutants. In this study, vertical profiles of aerosol extinction coefficient, nitrogen dioxide (NO2) and formaldehyde (HCHO) concentrations were retrieved from MAX-DOAS measurements using the Heidelberg Profile (HEIPRO) algorithm, while vertical distribution of ozone (O3) was obtained from an ozone lidar. Sensitivity study of the MAX-DOAS aerosol profile retrieval shows that the a priori aerosol profile shape has significant influences on the aerosol profile retrieval. Aerosol profiles retrieved from MAX-DOAS measurements with Gaussian a priori profile demonstrate the best agreements with simultaneous lidar measurements and vehicle-based tethered-balloon observations among all a priori aerosol profiles. Tropospheric NO2 vertical column densities (VCDs) measured with MAX-DOAS show a good agreement with OMI satellite observations with a Pearson correlation coefficient (R) of 0.95. In addition, measurements of the O3 vertical distribution indicate that the ozone productions do not only occur at surface level but also at higher altitudes (about 1.1 km). Planetary boundary layer (PBL) height and horizontal and vertical wind field information were integrated to discuss the ozone formation at upper altitudes. The results reveal that enhanced ozone concentrations at ground level and upper altitudes are not directly related to horizontal and vertical transportation. Similar patterns of O3 and HCHO vertical distributions were observed during this campaign, which implies that the ozone productions near the surface and at higher altitudes are mainly influenced by the abundance of volatile organic compounds (VOCs) in the lower troposphere.

A new diagnostic for tropospheric ozone production

Science.gov (United States)

Edwards, Peter M.; Evans, Mathew J.

2017-11-01

Tropospheric ozone is important for the Earth's climate and air quality. It is produced during the oxidation of organics in the presence of nitrogen oxides. Due to the range of organic species emitted and the chain-like nature of their oxidation, this chemistry is complex and understanding the role of different processes (emission, deposition, chemistry) is difficult. We demonstrate a new methodology for diagnosing ozone production based on the processing of bonds contained within emitted molecules, the fate of which is determined by the conservation of spin of the bonding electrons. Using this methodology to diagnose ozone production in the GEOS-Chem chemical transport model, we demonstrate its advantages over the standard diagnostic. We show that the number of bonds emitted, their chemistry and lifetime, and feedbacks on OH are all important in determining the ozone production within the model and its sensitivity to changes. This insight may allow future model-model comparisons to better identify the root causes of model differences.

A new diagnostic for tropospheric ozone production

Directory of Open Access Journals (Sweden)

P. M. Edwards

2017-11-01

Full Text Available Tropospheric ozone is important for the Earth's climate and air quality. It is produced during the oxidation of organics in the presence of nitrogen oxides. Due to the range of organic species emitted and the chain-like nature of their oxidation, this chemistry is complex and understanding the role of different processes (emission, deposition, chemistry is difficult. We demonstrate a new methodology for diagnosing ozone production based on the processing of bonds contained within emitted molecules, the fate of which is determined by the conservation of spin of the bonding electrons. Using this methodology to diagnose ozone production in the GEOS-Chem chemical transport model, we demonstrate its advantages over the standard diagnostic. We show that the number of bonds emitted, their chemistry and lifetime, and feedbacks on OH are all important in determining the ozone production within the model and its sensitivity to changes. This insight may allow future model–model comparisons to better identify the root causes of model differences.

Impacts of Interannual Variability in Biogenic VOC Emissions near Transitional Ozone Production Regimes

Science.gov (United States)

Geddes, J.

2017-12-01

Due to successful NOx emission controls, summertime ozone production chemistry in urban areas across North America is transitioning from VOC-limited to increasingly NOx-limited. In some regions where ozone production sensitivity is in transition, interannual variability in surrounding biogenic VOC emissions could drive fluctuations in the prevailing chemical regime and modify the impact of anthropogenic emission changes. I use satellite observations of HCHO and NO2 column density, along with a long-term simulation of atmospheric chemistry, to investigate the impact of interannual variability in biogenic isoprene sources near large metro areas. Peak emissions of isoprene in the model can vary by up to 20-60% in any given year compared to the long term mean, and this variability drives the majority of the variability in simulated local HCHO:NO2 ratios (a common proxy for ozone production sensitivity). The satellite observations confirm increasingly NOx-limited chemical regimes with large interannual variability. In several instances, the model and satellite observations suggest that variability in biogenic isoprene emissions could shift summertime ozone production from generally VOC- to generally NOx- sensitive (or vice versa). This would have implications for predicting the air quality impacts of anthropogenic emission changes in any given year, and suggests that drivers of biogenic emissions need to be well understood.

Kinetics of nitrosamine and amine reactions with NO3 radical and ozone related to aqueous particle and cloud droplet chemistry

Science.gov (United States)

Weller, Christian; Herrmann, Hartmut

2015-01-01

Aqueous phase reactivity experiments with the amines dimethylamine (DMA), diethanolamine (DEA) and pyrrolidine (PYL) and their corresponding nitrosamines nitrosodimethylamine (NDMA), nitrosodiethanolamine (NDEA) and nitrosopyrrolidine (NPYL) have been performed. NO3 radical reaction rate coefficients for DMA, DEA and PYL were measured for the first time and are 3.7 × 105, 8.2 × 105 and 8.7 × 105 M-1 s-1, respectively. Rate coefficients for NO3 + NDMA, NDEA and NPYL are 1.2 × 108, 2.3 × 108 and 2.4 × 108 M-1 s-1. Compared to OH radical rate coefficients for reactions with amines, the NO3 radical will most likely not be an important oxidant but it is a potential nighttime oxidant for nitrosamines in cloud droplets or deliquescent particles. Ozone is unreactive towards amines and nitrosamines and upper limits of rate coefficients suggest that aqueous ozone reactions are not important in atmospheric waters.

Production and Transport of Ozone From Boreal Forest Fires

Science.gov (United States)

Tarasick, David; Liu, Jane; Osman, Mohammed; Sioris, Christopher; Liu, Xiong; Najafabadi, Omid; Parrington, Mark; Palmer, Paul; Strawbridge, Kevin; Duck, Thomas

2013-04-01

In the summer of 2010, the BORTAS (Quantifying the impact of BOReal forest fires on Tropospheric oxidants over the Atlantic using Aircraft and Satellites) mission was planned by several universities and government agencies in the United Kingdom, Canada, and USA. Nearly 100 ozone soundings were made at 13 stations through the BORTAS Intensive Sounding Network, although aircraft measurements were unfortunately cancelled due to the volcanic eruption in Iceland. 2010 was actually an exceptional year for Canadian boreal fires. MODIS (Moderate Resolution Imaging Spectroradiometer) fire count data shows large fire events in Saskatchewan on several days in July. High amounts of NO2 close to the large fires are observed from OMI satellite data, indicating that not all NO2 is converted to PAN. Also associated with the fires, large amounts of CO, another precursor of ozone, are observed in MOPITT (Measurements Of Pollution In The Troposphere), AIRS and TES (Tropospheric Emission Spectrometer) satellite data in the middle to upper troposphere. These chemical conditions combined with sunny weather all favour ozone production. Following days with large fire activity, layers of elevated ozone mixing ratio (over 100 ppbv) are observed downwind at several sites. Back-trajectories suggest the elevated ozone in the profile is traceable to the fires in Saskatchewan. Lidar profiles also detect layers of aerosol at the same heights. However, the layers of high ozone are also associated with low humidity, which is not expected from a combustion source, and suggests the possibility of entrainment of stratospheric air.

Pulsed Streamer Discharge Characteristics of Ozone Production in Dry Air

OpenAIRE

Samaranayake, W.J.M.; Miyahara, Y.; Namihira, T.; Katsuki, S.; Sakugawa, T.; Hackam, R.; Akiyama, H.; ナミヒラ, タカオ; カツキ, スナオ; アキヤマ, ヒデノリ; 波平, 隆男; 勝木, 淳; 秋山, 秀典

2000-01-01

Experimental investigation of HV short pulsed streamer discharges in dry air-fed ozonizers under various operating conditions are reported. Ozone concentration, energy input and ozone production yield (efficiency) were measured at various voltages (14 to 37 kV), pulse repetition rates (25 to 400 pulses per second, pps), flow rates (1.5 to 3.0 1/min) and different gap spacings (10 to 20 mm) at a pressure of 1.01×105 Pa in dry air. A spiral copper wire (1 mm in diameter) made to a cylindrical c...

Personal exposure to metal fume, NO2, and O3 among production welders and non-welders.

Science.gov (United States)

Schoonover, Todd; Conroy, Lorraine; Lacey, Steven; Plavka, Julie

2011-01-01

The objective of this study was to characterize personal exposures to welding-related metals and gases for production welders and non-welders in a large manufacturing facility. Welding fume metals and irritant gases nitrogen dioxide (NO(2)) and ozone (O(3)) were sampled for thirty-eight workers. Personal exposure air samples for welding fume metals were collected on 37 mm open face cassettes and nitrogen dioxide and ozone exposure samples were collected with diffusive passive samplers. Samples were analyzed for metals using Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and welding fume metal exposure concentrations were defined as the sum of welding-related metals mass per volume of air sampled. Welding fume metal exposures were highly variable among similar types of welding while NO(2) and O(3) exposure were less variable. Welding fume metal exposures were significantly higher 474 μg/m(3) for welders than non-welders 60 μg/m(3) (p=0.001). Welders were exposed to higher concentrations of NO(2) and O(3) than non-welders but the differences were not statistically significant. Welding fume metal exposure concentrations for welders performing gas metal arc welding (GMAW) and shielded metal arc welding (SMAW) were higher than welders performing gas tungsten arc welding (GTAW). Non-welders experienced exposures similar to GTAW welders despite a curtain wall barrier separating welding and non-welding work areas.

Measurement of ozone production scaling in a helium plasma jet with oxygen admixture

Science.gov (United States)

Sands, Brian; Ganguly, Biswa

2012-10-01

Capillary dielectric barrier plasma jet devices that generate confined streamer-like discharges along a rare gas flow can produce significant quantities of reactive oxygen species with average input powers ranging from 100 mW to >1 W. We have measured spatially-resolved ozone production in a He plasma jet with O2 admixture concentrations up to 5% using absorption spectroscopy of the O3 Hartley band system. A 20-ns risetime, 10-13 kV positive unipolar voltage pulse train was used to power the discharge, with pulse repetition rates varied from 1-20 kHz. The discharge was operated in a transient glow mode to scale the input power by adjusting the gap width between the anode and downstream cathodic plane. Peak ozone number densities in the range of 10^16 - 10^17 cm-3 were measured. At a given voltage, the density of ozone increased monotonically up to 3% O2 admixture (6 mm gap) as the peak discharge current decreased by an order of magnitude. Ozone production increased with distance from the capillary, consistent with observations by other groups. Atomic oxygen production inferred from O-atom 777 nm emission intensity did not scale with ozone as the input power was increased. The spatial distribution of ozone and scaling with input power will be presented.

Ozone flux over a Norway spruce forest and correlation with net ecosystem production

International Nuclear Information System (INIS)

Zapletal, Milos; Cudlin, Pavel; Chroust, Petr; Urban, Otmar; Pokorny, Radek; Edwards-Jonasova, Magda; Czerny, Radek; Janous, Dalibor; Taufarova, Klara; Vecera, Zbynek; Mikuska, Pavel; Paoletti, Elena

2011-01-01

Daily ozone deposition flux to a Norway spruce forest in Czech Republic was measured using the gradient method in July and August 2008. Results were in good agreement with a deposition flux model. The mean daily stomatal uptake of ozone was around 47% of total deposition. Average deposition velocity was 0.39 cm s -1 and 0.36 cm s -1 by the gradient method and the deposition model, respectively. Measured and modelled non-stomatal uptake was around 0.2 cm s -1 . In addition, net ecosystem production (NEP) was measured by using Eddy Covariance and correlations with O 3 concentrations at 15 m a.g.l., total deposition and stomatal uptake were tested. Total deposition and stomatal uptake of ozone significantly decreased NEP, especially by high intensities of solar radiation. - Highlights: → We estimate ozone deposition flux to a Norway spruce forest using the gradient method and model. → The mean stomatal uptake of ozone is approximately 47% of the total deposition. → We measure net ecosystem production (NEP) using Eddy Covariance. → We test whether elevated total deposition and stomatal uptake of O 3 imply a reduction of NEP. → Deposition and stomatal uptake of O 3 decrease NEP, especially by high intensities of solar radiation. - Net ecosystem production of a Norway spruce forest decreases with increasing deposition and stomatal uptake of ozone.

Higher measured than modeled ozone production at increased NOx levels in the Colorado Front Range

Directory of Open Access Journals (Sweden)

B. C. Baier

2017-09-01

Full Text Available Chemical models must correctly calculate the ozone formation rate, P(O3, to accurately predict ozone levels and to test mitigation strategies. However, air quality models can have large uncertainties in P(O3 calculations, which can create uncertainties in ozone forecasts, especially during the summertime when P(O3 is high. One way to test mechanisms is to compare modeled P(O3 to direct measurements. During summer 2014, the Measurement of Ozone Production Sensor (MOPS directly measured net P(O3 in Golden, CO, approximately 25 km west of Denver along the Colorado Front Range. Net P(O3 was compared to rates calculated by a photochemical box model that was constrained by measurements of other chemical species and that used a lumped chemical mechanism and a more explicit one. Median observed P(O3 was up to a factor of 2 higher than that modeled during early morning hours when nitric oxide (NO levels were high and was similar to modeled P(O3 for the rest of the day. While all interferences and offsets in this new method are not fully understood, simulations of these possible uncertainties cannot explain the observed P(O3 behavior. Modeled and measured P(O3 and peroxy radical (HO2 and RO2 discrepancies observed here are similar to those presented in prior studies. While a missing atmospheric organic peroxy radical source from volatile organic compounds co-emitted with NO could be one plausible solution to the P(O3 discrepancy, such a source has not been identified and does not fully explain the peroxy radical model–data mismatch. If the MOPS accurately depicts atmospheric P(O3, then these results would imply that P(O3 in Golden, CO, would be NOx-sensitive for more of the day than what is calculated by models, extending the NOx-sensitive P(O3 regime from the afternoon further into the morning. These results could affect ozone reduction strategies for the region surrounding Golden and possibly other areas that do not comply with national ozone

Observations of NO2 and O3 during thunderstorm activity using visible spectroscopy

Science.gov (United States)

Jadhav, D. B.; Londhe, A. L.; Bose, S.

1996-08-01

Simultaneous observations for the total column densities of NO2 , O3 and H2O were carried on using the portable Spectrometer (438-450 nm and 400-450 nm) and the visible Spectrometer (544.4-628 nm) during premonsoon thunderstorms and embedded hail storm activity at Pune (18°32’N & 73°51’E), India. These observations confirm the fact that there is an increase in O3 and NO2 column densities during thunderstorms. The increase in O3 was observed following onset of thunderstorm, while the increase in NO2 was observed only after the thunder flashes occur. This implies that the production mechanisms for O3 and NO2 in thunderstorm are different. The observed column density of NO2 value (1 to 3 × 1017molecules · cm-2) during thunderstorm activity is 10 to 30 times higher than the value (1 × 1016molecules · cm-2) of a normal day total column density. The spectrometric observations and observations of thunder flashes by electric field meter showed that 6.4 × 1025molecules / flash of NO2 are produced. The increased total column density of ozone during thunderstorm period is 1.2 times higher than normal (clear) day ozone concentration. The multiple scattering in the clouds is estimated from H2O and O2 absorption bands in the visible spectral region. Considering this effect the calculated amount of ozone added in the global atmosphere due to thunderstorm activity is 0.26 to 0.52 DU, and the annual production of ozone due to thunderstorm activity is of the order of 4.02 × 1037 molecules / year. The annual NO2 production may be of the order of 2.02 × 1035molecules / year.

Ozone production in a dielectric barrier discharge with ultrasonic irradiation

DEFF Research Database (Denmark)

Drews, Joanna Maria; Kusano, Yukihiro; Leipold, Frank

2011-01-01

Ozone production has been investigated using an atmospheric pressure dielectric barrier discharge in pure O2 at room temperature with and without ultrasonic irradiation. It was driven at a frequency of either 15 kHz or 40 kHz. The ozone production was highly dependent on the O2 flow rate and the ......Ozone production has been investigated using an atmospheric pressure dielectric barrier discharge in pure O2 at room temperature with and without ultrasonic irradiation. It was driven at a frequency of either 15 kHz or 40 kHz. The ozone production was highly dependent on the O2 flow rate...

Diurnal variations in H2O2, O3, PAN, HNO3 and aldehyde concentrations and NO/NO2 ratios at Rishiri Island, Japan: Potential influence from iodine chemistry

International Nuclear Information System (INIS)

Kanaya, Yugo; Tanimoto, Hiroshi; Matsumoto, Jun; Furutani, Hiroshi; Hashimoto, Shigeru; Komazaki, Yuichi; Tanaka, Shigeru; Yokouchi, Yoko; Kato, Shungo; Kajii, Yoshizumi; Akimoto, Hajime

2007-01-01

The presence of iodine chemistry, hypothesized due to the overprediction of HO 2 levels by a photochemical box model at Rishiri Island in June 2000, was quantitatively tested against the observed NO/NO 2 ratios and the net production rates of ozone. The observed NO/NO 2 ratios were reproduced reasonably well by considering the conversion of NO to NO 2 by IO, whose amount was calculated so as to reproduce the observed HO 2 levels. However, the net production rates of ozone were calculated to be negative when such high mixing ratios of IO were considered, which was inconsistent with the observed buildup of ozone during daytime. These results suggest that iodine chemistry may not be the sole mechanism for the reduced mixing ratios of HO 2 , or that 'hot spots' for iodine chemistry were present. Diurnal variations in the mixing ratios of HCHO, CH 3 CHO, peroxy acetyl nitrate (PAN) and HNO 3 observed during the study are presented along with the simulated ones. The box model simulations suggest that the effect of iodine chemistry on these concentrations is small and that important sources of CH 3 CHO and sinks of PAN are probably missing from our current understanding of the tropospheric chemistry mechanism

Indoor secondary pollutants from cleaning product and air freshener use in the presence of ozone

DEFF Research Database (Denmark)

Singer, B.C.; Coleman, B.K.; Destaillats, H.

2006-01-01

introduction. In the absence of reactive chemicals, the chamber ozone level was approximately 60 ppb. Ozone was substantially consumed following cleaning product use, mainly by homogeneous reaction. For the AFR, ozone consumption was weaker and heterogeneous reaction with sorbed AFR-constituent VOCs...... than 100 mu g m(-3)) in some experiments. Ozone consumption and elevated hydroxyl radical concentrations persisted for 10-12 h following brief cleaning events, indicating that secondary pollutant production can persist for extended periods. (c) 2006 Elsevier Ltd. All rights reserved....

OZONE PRECURSORS, SOURCE REGIONS, AND O(3) FORMATION DURING THE TEXAQS 2000 STUDY

International Nuclear Information System (INIS)

DAUM, P.H.; KLEINMAN, L.I.; BRECHTEL, F.; LEE, Y.N.; NUNNERMACKER, L.J.; SPRINGSTON, S.R.; WEINSTEIN-LLOYD, J.

2001-01-01

The DOE G-1 aircraft made flights on 14 days during the TexAQS 2000 study. On 7 of those days, the aircraft encountered highly localized plumes exhibiting O(sub 3) concentrations in excess of 150 ppb; on some days, peak O(sub 3) concentrations were in excess of 200 ppb. These ozone plumes were rapidly formed with an efficiency (O(sub 3) per NO(sub x) molecule consumed) much higher (7-20) than observed in other urban areas (3-4), and were frequently associated with high concentrations ( and gt;20 ppb) of secondary hydrocarbon species such as formaldehyde. Back trajectory analysis showed that the plumes were invariably associated with emissions from one or more of the large industrial complexes clustered about the Houston Ship Channel and Galveston Bay. Very high hydrocarbon reactivities were found in the vicinity of these facilities during morning flights. These hydrocarbon reactivities, in combination with local NO(sub x) emissions, were large enough to support instantaneous O(sub 3) production rates as high as 200 ppb/h. It is hypothesized that the combination of nitrogen oxides and hydrocarbon emissions emanating from this complex of industries provided a potent mixture of chemicals that caused the rapid formation of very high concentrations of ozone which, depending on the prevailing meteorology, could cause exceedance of the NAAQS ozone standard anywhere in the Houston metropolitan area

Evaluation of ozone emissions and exposures from consumer products and home appliances.

Science.gov (United States)

Zhang, Q; Jenkins, P L

2017-03-01

Ground-level ozone can cause serious adverse health effects and environmental impacts. This study measured ozone emissions and impacts on indoor ozone levels and associated exposures from 17 consumer products and home appliances that could emit ozone either intentionally or as a by-product of their functions. Nine products were found to emit measurable ozone, one up to 6230 ppb at a distance of 5 cm (2 inches). One use of these products increased room ozone concentrations by levels up to 106 ppb (mean, from an ozone laundry system) and personal exposure concentrations of the user by 12-424 ppb (mean). Multiple cycles of use of one fruit and vegetable washer increased personal exposure concentrations by an average of 2550 ppb, over 28 times higher than the level of the 1-h California Ambient Air Quality Standard for ozone (0.09 ppm). Ozone emission rates ranged from 1.6 mg/h for a refrigerator air purifier to 15.4 mg/h for a fruit and vegetable washer. The use of some products was estimated to contribute up to 87% of total daily exposures to ozone. The results show that the use of some products may result in potential health impacts. © 2016 The Authors. Indoor Air published by John Wiley & Sons Ltd.

Trans-Pacific transport of reactive nitrogen and ozone to Canada during spring

Directory of Open Access Journals (Sweden)

T. W. Walker

2010-09-01

Full Text Available We interpret observations from the Intercontinental Chemical Transport Experiment, Phase B (INTEX-B in spring 2006 using a global chemical transport model (GEOS-Chem to evaluate sensitivities of the free troposphere above the North Pacific Ocean and North America to Asian anthropogenic emissions. We develop a method to use satellite observations of tropospheric NO₂ columns to provide timely estimates of trends in NO_x emissions. NO_x emissions increased by 33% for China and 29% for East Asia from 2003 to 2006. We examine measurements from three aircraft platforms from the INTEX-B campaign, including a Canadian Cessna taking vertical profiles of ozone near Whistler Peak. The contribution to the mean simulated ozone profiles over Whistler below 5.5 km is at least 7.2 ppbv for Asian anthropogenic emissions and at least 3.5 ppbv for global lightning NO_x emissions. Tropospheric ozone columns from OMI exhibit a broad Asian outflow plume across the Pacific, which is reproduced by simulation. Mean modelled sensitivities of Pacific (30° N–60° N tropospheric ozone columns are at least 4.6 DU for Asian anthropogenic emissions and at least 3.3 DU for lightning, as determined by simulations excluding either source. Enhancements of ozone over Canada from Asian anthropogenic emissions reflect a combination of trans-Pacific transport of ozone produced over Asia, and ozone produced in the eastern Pacific through decomposition of peroxyacetyl nitrates (PANs. A sensitivity study decoupling PANs globally from the model's chemical mechanism establishes that PANs increase ozone production by removing NO_x from regions of low ozone production efficiency (OPE and injecting it into regions with higher OPE, resulting in a global increase in ozone production by 2% in spring 2006. PANs contribute up to 4 ppbv to surface springtime ozone concentrations in western Canada. Ozone production due to PAN transport is

Comparison of ultraviolet absorbance and NO-chemiluminescence for ozone measurement in wildfire plumes at the Mount Bachelor Observatory

Science.gov (United States)

Gao, Honglian; Jaffe, Daniel A.

2017-10-01

The goal of this paper is to evaluate the accuracy of the commonly used ozone (O3) instrument (the ultraviolet (UV) photometer) against a Federal Reference Method (Nitric Oxide -chemiluminescence) for ozone measurement in wildfire smoke plumes. We carried out simultaneous ozone measurement with two UV O3 photometers and one nitric oxide-chemiluminescence (NO-CL) ozone detectors during wildfire season (Aug. 1-Sept. 30) in 2015 at the Mount Bachelor Observatory (MBO, 2763 m above mean sea level, Oregon, USA). The UV O3 shows good agreement and excellent correlation to NO-CL O3, with linear regression slopes close to unity and R2 of 0.92 for 1-h average data and R2 of 0.93 for O3 daily maximum 8-h average (MDA8). During this two-month period we identified 35 wildfire events. Ozone enhancements in those wildfire plumes measured by NO-CL O3 and UV O3 monitors also show good agreement and excellent linear correlation, with a slope and R2 of 1.03 and 0.86 for O3 enhancements (ΔO3) and 1.00 and 0.98 for carbon monoxide (CO)-normalized ozone enhancement ratios (ΔO3/ΔCO), respectively. Overall, the UV O3 was found to have a positive bias of 4.7 ± 2.8 ppbv compared to the NO-CL O3. The O3 bias between NO-CL O3 and UV O3 is independent of wildfire plume tracers such as CO, particulate matter (PM1), aerosol scattering, and ultrafine particles. The results demonstrate that the UV O3 absorbance method is reliable, even in highly concentrated wildfire plumes.

Quantifying the Impact of Tropospheric Ozone on Crops Productivity at regional scale using JULES-crop

Science.gov (United States)

Leung, F.

2016-12-01

Tropospheric ozone (O3) is the third most important anthropogenic greenhouse gas. It is causing significant crop production losses. Currently, O3 concentrations are projected to increase globally, which could have a significant impact on food security. The Joint UK Land Environment Simulator modified to include crops (JULES-crop) is used here to quantify the impacts of tropospheric O3 on crop production at the regional scale until 2100. We evaluate JULES-crop against the Soybean Free-Air-Concentration-Enrichment (SoyFACE) experiment in Illinois, USA. Experimental data from SoyFACE and various literature sources is used to calibrate the parameters for soybean and ozone damage parameters in soybean in JULES-crop. The calibrated model is then applied for a transient factorial set of JULES-crop simulations over 1960-2005. Simulated yield changes are attributed to individual environmental drivers, CO2, O3 and climate change, across regions and for different crops. A mixed scenario of RCP 2.6 and RCP 8.5 climatology and ozone are simulated to explore the implication of policy. The overall findings are that regions with high ozone concentration such as China and India suffer the most from ozone damage, soybean is more sensitive to O3 than other crops. JULES-crop predicts CO2 fertilisation would increase the productivity of vegetation. This effect, however, is masked by the negative impacts of tropospheric O3. Using data from FAO and JULES-crop estimated that ozone damage cost around 55.4 Billion USD per year on soybean. Irrigation improves the simulation of rice only, and it increases the relative ozone damage because drought can reduce the ozone from entering the plant stomata. RCP 8.5 scenario results in a high yield for all crops mainly due to the CO2 fertilisation effect. Mixed climate scenarios simulations suggest that RCP 8.5 CO2 concentration and RCP 2.6 O3 concentration result in the highest yield. Further works such as more crop FACE-O3 experiments and more Crop

Numerical Study of the Simultaneous Oxidation of NO and SO2 by Ozone

Science.gov (United States)

Li, Bo; Zhao, Jinyang; Lu, Junfu

2015-01-01

This study used two kinetic mechanisms to evaluate the oxidation processes of NO and SO2 by ozone. The performance of the two models was assessed by comparisons with experimental results from previous studies. The first kinetic mechanism was a combined model developed by the author that consisted of 50 species and 172 reactions. The second mechanism consisted of 23 species and 63 reactions. Simulation results of both of the two models show under predictions compared with experimental data. The results showed that the optimized reaction temperature for NO with O3 ranged from 100~200 °C. At higher temperatures, O3 decomposed to O2 and O, which resulted in a decrease of the NO conversion rate. When the mole ratio of O3/NO was greater than 1, products with a higher oxidation state (such as NO3, N2O5) were formed. The reactions between O3 and SO2 were weak; as such, it was difficult for O3 to oxidize SO2. PMID:25642689

Observations of the vertical distributions of summertime atmospheric pollutants and the corresponding ozone production in Shanghai, China

Directory of Open Access Journals (Sweden)

C. Xing

2017-12-01

Full Text Available Ground-based multi-axis differential optical absorption spectroscopy (MAX-DOAS and lidar measurements were performed in Shanghai, China, during May 2016 to investigate the vertical distribution of summertime atmospheric pollutants. In this study, vertical profiles of aerosol extinction coefficient, nitrogen dioxide (NO2 and formaldehyde (HCHO concentrations were retrieved from MAX-DOAS measurements using the Heidelberg Profile (HEIPRO algorithm, while vertical distribution of ozone (O3 was obtained from an ozone lidar. Sensitivity study of the MAX-DOAS aerosol profile retrieval shows that the a priori aerosol profile shape has significant influences on the aerosol profile retrieval. Aerosol profiles retrieved from MAX-DOAS measurements with Gaussian a priori profile demonstrate the best agreements with simultaneous lidar measurements and vehicle-based tethered-balloon observations among all a priori aerosol profiles. Tropospheric NO2 vertical column densities (VCDs measured with MAX-DOAS show a good agreement with OMI satellite observations with a Pearson correlation coefficient (R of 0.95. In addition, measurements of the O3 vertical distribution indicate that the ozone productions do not only occur at surface level but also at higher altitudes (about 1.1 km. Planetary boundary layer (PBL height and horizontal and vertical wind field information were integrated to discuss the ozone formation at upper altitudes. The results reveal that enhanced ozone concentrations at ground level and upper altitudes are not directly related to horizontal and vertical transportation. Similar patterns of O3 and HCHO vertical distributions were observed during this campaign, which implies that the ozone productions near the surface and at higher altitudes are mainly influenced by the abundance of volatile organic compounds (VOCs in the lower troposphere.

Influencing factors on microbubble ozonation treatment of acid red 3R wastewater

Directory of Open Access Journals (Sweden)

Yurong YA

2017-08-01

Full Text Available The microbubble ozonation was used to treat acid red 3R wastewater in order to investigate the influencing factors on its performance. The effects of ozone dose, initial acid red 3R concentration and activated carbon on the performance of microbubble ozonation treatment of acid red 3R wastewater are investigated. The decolorization rate, TOC removal rate, pH variation and ozone utilization efficiency in the microbubble ozonation treatment are compared under different treatment conditions. The results indicate that when increasing ozone dose or decreasing initial acid red 3R concentration, both decolorization rate and TOC removal rate of acid red 3R wastewater increase, but ozone utilization efficiency decreases. The coal-based activated carbon shows strong catalytic activity for microbubble ozonation, which could enhance the decolorization rate and TOC removal rate of acid red 3R wastewater. The better performance of microbubble ozonation treatment is achieved when the ozone dose is 48.3 mg/min and the initial acid red 3R mass concentration is 100 mg/L. Under these conditions, the decolorization efficiency reaches to 100% after treatment for 30 min, the TOC removal efficiency reaches to 78.0% after treatment for 120 min, the reaction rate constant of TOC removal is 0.015 min^-1 and the ozone utilization efficiency is higher than 99%. With addition of the coal-based activated carbon of 5 g/L, the decolorization efficiency reaches to 100% after treatment for 15 min, the TOC removal efficiency reaches to 91.2% after treatment for 120 min and the reaction rate constant of TOC removal increases to 0037 min^-1.The accumulation and following degradation of intermediate products of small molecule organic acid happens during treatment process, and as a result, the solution pH decreases initially and then increases. Therefore, the optimization of influencing factors for microbubble ozonation could increase both contaminant removal

Ozone Production in Global Tropospheric Models: Quantifying Errors due to Grid Resolution

Science.gov (United States)

Wild, O.; Prather, M. J.

2005-12-01

Ozone production in global chemical models is dependent on model resolution because ozone chemistry is inherently nonlinear, the timescales for chemical production are short, and precursors are artificially distributed over the spatial scale of the model grid. In this study we examine the sensitivity of ozone, its precursors, and its production to resolution by running a global chemical transport model at four different resolutions between T21 (5.6° × 5.6°) and T106 (1.1° × 1.1°) and by quantifying the errors in regional and global budgets. The sensitivity to vertical mixing through the parameterization of boundary layer turbulence is also examined. We find less ozone production in the boundary layer at higher resolution, consistent with slower chemical production in polluted emission regions and greater export of precursors. Agreement with ozonesonde and aircraft measurements made during the NASA TRACE-P campaign over the Western Pacific in spring 2001 is consistently better at higher resolution. We demonstrate that the numerical errors in transport processes at a given resolution converge geometrically for a tracer at successively higher resolutions. The convergence in ozone production on progressing from T21 to T42, T63 and T106 resolution is likewise monotonic but still indicates large errors at 120~km scales, suggesting that T106 resolution is still too coarse to resolve regional ozone production. Diagnosing the ozone production and precursor transport that follow a short pulse of emissions over East Asia in springtime allows us to quantify the impacts of resolution on both regional and global ozone. Production close to continental emission regions is overestimated by 27% at T21 resolution, by 13% at T42 resolution, and by 5% at T106 resolution, but subsequent ozone production in the free troposphere is less significantly affected.

Evaluating a Space-Based Indicator of Surface Ozone-NO x -VOC Sensitivity Over Midlatitude Source Regions and Application to Decadal Trends.

Science.gov (United States)

Jin, Xiaomeng; Fiore, Arlene M; Murray, Lee T; Valin, Lukas C; Lamsal, Lok N; Duncan, Bryan; Boersma, K Folkert; De Smedt, Isabelle; Abad, Gonzalo Gonzalez; Chance, Kelly; Tonnesen, Gail S

2017-10-16

Determining effective strategies for mitigating surface ozone (O 3 ) pollution requires knowledge of the relative ambient concentrations of its precursors, NO x , and VOCs. The space-based tropospheric column ratio of formaldehyde to NO 2 (FNR) has been used as an indicator to identify NO x -limited versus NO x -saturated O 3 formation regimes. Quantitative use of this indicator ratio is subject to three major uncertainties: (1) the split between NO x -limited and NO x -saturated conditions may shift in space and time, (2) the ratio of the vertically integrated column may not represent the near-surface environment, and (3) satellite products contain errors. We use the GEOS-Chem global chemical transport model to evaluate the quantitative utility of FNR observed from the Ozone Monitoring Instrument over three northern midlatitude source regions. We find that FNR in the model surface layer is a robust predictor of the simulated near-surface O 3 production regime. Extending this surface-based predictor to a column-based FNR requires accounting for differences in the HCHO and NO 2 vertical profiles. We compare four combinations of two OMI HCHO and NO 2 retrievals with modeled FNR. The spatial and temporal correlations between the modeled and satellite-derived FNR vary with the choice of NO 2 product, while the mean offset depends on the choice of HCHO product. Space-based FNR indicates that the spring transition to NO x -limited regimes has shifted at least a month earlier over major cities (e.g., New York, London, and Seoul) between 2005 and 2015. This increase in NO x sensitivity implies that NO x emission controls will improve O 3 air quality more now than it would have a decade ago.

Ozone, OH and NO3 sink terms at a coniferous forest site in Central Germany: Role of biogenic VOCs

Science.gov (United States)

Bonn, B.; Bourtsoukidis, S.; Haunold, W.; Sitals, R.; Jacobi, S.

2012-04-01

sink terms during daytime. The contributions of monoterpene and isoprene reactions strengthened towards the summer period, while sesquiterpene reactions slowed down. Hydroxyl radical: The picture becomes much more complex for OH. Besides the reaction with nitrogen dioxide, isoprene and monoterpenes were key destructing agents of OH with estimated contributions of about 50-60%, increasing towards the summertime. Contributions of their oxidation products to the total sink of OH are supposed to be less than 20% but showing more intense during summer and less towards cooler periods. Sesquiterpene OH-reactions only contributed to 10% with a maximum of about 20% at the early April. Nitrate radical: NO3 displayed a mixture of the sinks of OH and ozone. The dominant destruction takes place via NOx-reactions (about 50%) and the remainder primarily via monoterpene (36±20%), sesquiterpene (11±8%) and isoprene (2±1%) OH-reactions. From our observations at this particular site it is apparent that the spruce forest provides a quite efficient variety of pathways to compensate oxidation stress. This is essentially displayed in the variation of emission pattern of different compound classes with different reactivity for the three major oxidation agents. One needs to be aware of the fact that the sink is highly variable in space, too. Therefore we conclude: In order to understand and describe the oxidation tolerance of a certain ecosystem one needs to detect at least the reactive hydrocarbons. [1] Jenkin, M.E., Shallcross, D. E., and Harvey, J. N.: Development and application of a possible mechanism for the generation of cis-pinic acid form the ozonolysis of α- and β-pinene. Atmos.Environ., 34, 2837-2850, 2000.

Effect of gaseous ozone for control of stored product pests at low and high temperature

DEFF Research Database (Denmark)

Hansen, Lise Stengård; Hansen, Peer; Vagn Jensen, Karl-Martin

2013-01-01

Gaseous ozone (O3) has shown potential for control of insects in stored grain. A previous laboratory study determined doses of ozone necessary to control freely exposed and internal stages of eleven stored product pest species at 20 C. In this study the impact of temperature on the effect of ozone...... was tested on two species of stored product pests: Sitophilus granarius and Plodia interpunctella. Insects were exposed to continuous flows of ozone in doses of approximately 33 ppm for 6 d or approximately 131 ppm for 8 d at low temperatures between 7.3 and 7.9 C and high temperatures between 29.6 and 31.......6 C, respectively. Results from the previous study conducted at 20 C were used in the data analysis. The result of the treatments was unaffected by the temperatures used in the study. Treatment with a high dose of ozone for 8 d led to full mortality in all stages of S. granarius and all stages of P...

Ozone production in the reaction of T2 and O2 gas: A comparison of experimental results and model predictions

International Nuclear Information System (INIS)

Failor, R.A.; Souers, P.C.; Magnotta, F.

1992-01-01

Ozone, predicted to be an important intermediate species in T 2 oxidation, was monitored in situ by UV absorption spectroscopy for 0.01-1.0 mol % T 2 in O 2 (1 atm, 298 K). These are the first measurements of a tritium oxidation reaction intermediate. The experimental results were compared with the predictions of the author's comprehensive model of tritium oxidation. The experimentally determined temporal variation in ozone concentration is qualitatively reproduced by the model. As predicted, the measured initial rate of ozone production varied linearly with the initial T 2 concentration ([T 2 ] o ), but with a value one-third of that predicted. The steady-state ozone concentration ([O 3 ] ss ) a factor of 4 larger than predicted for a 1.0% T 2 -O 2 mixture. Addition of H 2 to the T 2 O 2 mixture, to differentiate between the radiolytic and chemical behavior of the tritium, produced a decrease in [O 3 ] ss which was larger than predicted. Changing the reaction cell surface-to-volume ratio showed indications of minor surface removal of ozone. No reasonable variation in model input parameters brought both the predicted initial ozone production rates and steady-state concentrations of ozone into agreement with the experimental results. Though qualitative agreement was achieved, further studies, with emphasis on surface effects, are necessary to explain quantitative differences and gain a greater understanding of the oxidation mechanism. 27 refs., 11 figs., 4 tabs

Indoor Secondary Pollutants from Household Product Emissions inthe Presence of Ozone: A Bench-Scale Chamber Study

Energy Technology Data Exchange (ETDEWEB)

Destaillats, Hugo; Lunden, Melissa M.; Singer, Brett C.; Coleman,Beverly K.; Hodgson, Alfred T.; Weschler, Charles J.; Nazaroff, William W.

2005-10-01

Ozone-driven chemistry is a major source of indoor secondary pollutants of health concern. This study investigates secondary air pollutants formed from reactions between constituents of household products and ozone. Gas-phase product emissions were introduced along with ozone at constant rates into a 198-L Teflon-lined reaction chamber. Gas-phase concentrations of reactive terpenoids and oxidation products were measured. Formaldehyde was a predominant oxidation byproduct for the three studied products, with yields under most conditions of 20-30% with respect to ozone consumed. Acetaldehyde, acetone, glycolaldehyde, formic acid and acetic acid were each also detected for two or three of the products. Immediately upon mixing of reactants, a scanning mobility particle sizer detected particle nucleation events that were followed by a significant degree of ultrafine particle growth. The production of secondary gaseous pollutants and particles depended primarily on the ozone level and was influenced by other parameters such as the air-exchange rate. Hydroxyl radical concentrations in the range 0.04-200 x 10{sup 5} molecules cm{sup -3} were measured. OH concentrations were observed to vary strongly with residual ozone level in the chamber, which was in the range 1-25 ppb, as is consistent with expectations from a simplified kinetic model. In a separate test, we exposed the dry residue of two products to ozone in the chamber and observed the formation of gas-phase and particle-phase secondary oxidation products.

Development and Application of Hyperspectral Infrared Ozone Retrieval Products for Operational Meteorology

Science.gov (United States)

Berndt, Emily; Zavodsky, Bradley; Jedlovec, Gary

2015-01-01

Cyclogenesis is a key forecast challenge at operational forecasting centers such as WPC and OPC, so these centers have a particular interest in unique products that can identify key storm features. In some cases, explosively developing extratropical cyclones can produce hurricane force, non-convective winds along the East Coast and north Atlantic as well as the Pacific Ocean, with the potential to cause significant damage to life and property. Therefore, anticipating cyclogenesis for these types of storms is crucial for furthering the NOAA goal of a "Weather Ready Nation". Over the last few years, multispectral imagery (i.e. RGB) products have gained popularity among forecasters. The GOES-R satellite champion at WPC/OPC has regularly evaluated the Air Mass RGB products from GOES Sounder, MODIS, and SEVIRI to aid in forecasting cyclogenesis as part of ongoing collaborations with SPoRT within the framework of the GOES-R Proving Ground. WPC/OPC has used these products to identify regions of stratospheric air associated with tropopause folds that can lead to cyclogenesis and hurricane force winds. RGB products combine multiple channels or channel differences into multi-color imagery in which different colors represent a particular cloud or air mass type. Initial interaction and feedback from forecasters evaluating the legacy Air Mass RGBs revealed some uncertainty regarding what physical processes the qualitative RGB products represent and color interpretation. To enhance forecaster confidence and interpretation of the Air Mass RGB, NASA SPoRT has transitioned a total column ozone product from AIRS retrievals to the WPC/OPC. The use of legacy AIRS demonstrates future JPSS capabilities possible with CrIS or OMPS. Since stratospheric air can be identified by anomalous potential vorticity and warm, dry, ozone-rich air, hyperspectral infrared sounder ozone products can be used in conjunction with the Air Mass RGB for identifying the role of stratospheric air in explosive

Demonstration of AIRS Total Ozone Products to Operations to Enhance User Readiness

Science.gov (United States)

Berndt, Emily; Zavodsky, Bradley; Jedlovec, Gary

2014-01-01

Cyclogenesis is a key forecast challenge at operational forecasting centers such as WPC and OPC, so these centers have a particular interest in unique products that can identify key storm features. In some cases, explosively developing extratropical cyclones can produce hurricane force, non-convective winds along the East Coast and north Atlantic as well as the Pacific Ocean, with the potential to cause significant damage to life and property. Therefore, anticipating cyclogenesis for these types of storms is crucial for furthering the NOAA goal of a "Weather Ready Nation". Over the last few years, multispectral imagery (i.e. RGB) products have gained popularity among forecasters. The GOES-R satellite champion at WPC/OPC has regularly evaluated the Air Mass RGB products from GOES Sounder, MODIS, and SEVIRI to aid in forecasting cyclogenesis as part of ongoing collaborations with SPoRT within the framework of the GOES-R Proving Ground. WPC/OPC has used these products to identify regions of stratospheric air associated with tropopause folds that can lead to cyclogenesis and hurricane force winds. RGB products combine multiple channels or channel differences into multi-color imagery in which different colors represent a particular cloud or air mass type. Initial interaction and feedback from forecasters evaluating the legacy Air Mass RGBs revealed some uncertainty regarding what physical processes the qualitative RGB products represent and color interpretation. To enhance forecaster confidence and interpretation of the Air Mass RGB, NASA SPoRT has transitioned a total column ozone product from AIRS retrievals to the WPC/OPC. The use of legacy AIRS demonstrates future JPSS capabilities possible with CrIS or OMPS. Since stratospheric air can be identified by anomalous potential vorticity and warm, dry, ozone-rich air, hyperspectral infrared sounder ozone products can be used in conjunction with the Air Mass RGB for identifying the role of stratospheric air in explosive

Impact of climate change on tropospheric ozone and its global budgets

Directory of Open Access Journals (Sweden)

G. Zeng

2008-01-01

Full Text Available We present the chemistry-climate model UM_CAM in which a relatively detailed tropospheric chemical module has been incorporated into the UK Met Office's Unified Model version 4.5. We obtain good agreements between the modelled ozone/nitrogen species and a range of observations including surface ozone measurements, ozone sonde data, and some aircraft campaigns.

Four 2100 calculations assess model responses to projected changes of anthropogenic emissions (SRES A2, climate change (due to doubling CO₂, and idealised climate change-associated changes in biogenic emissions (i.e. 50% increase of isoprene emission and doubling emissions of soil-NO_x. The global tropospheric ozone burden increases significantly for all the 2100 A2 simulations, with the largest response caused by the increase of anthropogenic emissions. Climate change has diverse impacts on O₃ and its budgets through changes in circulation and meteorological variables. Increased water vapour causes a substantial ozone reduction especially in the tropical lower troposphere (>10 ppbv reduction over the tropical ocean. On the other hand, an enhanced stratosphere-troposphere exchange of ozone, which increases by 80% due to doubling CO₂, contributes to ozone increases in the extratropical free troposphere which subsequently propagate to the surface. Projected higher temperatures favour ozone chemical production and PAN decomposition which lead to high surface ozone levels in certain regions. Enhanced convection transports ozone precursors more rapidly out of the boundary layer resulting in an increase of ozone production in the free troposphere. Lightning-produced NO_x increases by about 22% in the doubled CO₂ climate and contributes to ozone production.

The response to the increase of isoprene emissions shows that the change of ozone is largely determined by background NO_x levels: high

New Directions: Ozone-initiated reaction products indoors may be more harmful than ozone itself

Science.gov (United States)

Weschler, Charles J.

2004-10-01

Epidemiological studies have found associations between ozone concentrations measured at outdoor monitoring stations and certain adverse health outcomes. As a recent example, Gent et al. (2003, Journal of the American Medical Association 290, 1859-1867) have observed an association between ozone levels and respiratory symptoms as well as the use of maintenance medication by 271 asthmatic children living in Connecticut and the Springfield area of Massachusetts. In another example, Gilliland et al. (2001, Epidemiology 12, 43-54) detected an association between short-term increases in ozone levels and increased absences among 4th grade students from 12 southern California communities during the period from January to June 1996. Although children may spend a significant amount of time outdoors, especially during periods when ozone levels are elevated, they spend a much larger fraction of their time indoors. I hypothesize that exposure to the products of ozone-initiated indoor chemistry is more directly responsible for the health effects observed in the cited epidemiological studies than is exposure to outdoor ozone itself.

Ozone production and hydrocarbon reactivity in Hong Kong, Southern China

Directory of Open Access Journals (Sweden)

J. Zhang

2007-01-01

Full Text Available Data obtained in Hong Kong during the Hong Kong and the Pearl River Delta (PRD Pilot Air Monitoring Study in autumn 2002 are analyzed to unravel the relationship between ground-level ozone (O3, pollution precursors, and cross-border transport. Ten ozone episodes, during which the hourly O3 concentration exceeded 100 ppbv in 9 cases and 90 ppbv in one case, are subject to detailed analysis, including one case with hourly O3 of 203 ppbv, which is the highest concentration on record to date in Hong Kong. Combined with high-resolution back trajectories, dCO/dNOy (the ratio of enhancement of CO concentration above background to that of NOy is used to define whether O3 is locally or regionally produced. Five out of the ten Hong Kong O3-episodes studied show a "pollution signature" that is indicative of impact from Guangdong Province. Examination of speciated volatile organic compounds (VOCs shows that the reactivity of VOCs is dominated by anthropogenic VOCs, of which the reactive aromatics dominate, in particular xylenes and toluene. Calculations using a photochemical box model indicate that between 50–100% of the O3 increase observed in Hong Kong during the O3 episodes can be explained by photochemical generation within the Hong Kong area, provided that nitrous acid (HONO is present at the concentrations derived from this study. An Observation-Based Model (OBM is used to calculate the sensitivity of the O3 production to changes in the concentrations of the precursor compounds. Generally the production of O3 throughout much of the Hong Kong area is limited by VOCs, while high nitric oxide (NO concentrations suppress O3 concentration.

Ozone production by a dc corona discharge in air contaminated by n-heptane

International Nuclear Information System (INIS)

Pekarek, S

2008-01-01

Beneficial purposes of ozone such as elimination of odours, harmful bacteria and mildew can be used for transportation of food, fruits and vegetables with the aim to extend their storage life. To date the main technique used for this purpose in the transportation of these commodities, e.g. by trucks, was cooling. Here a combination of cooling together with the supply of ozone into containers with these commodities is considered. For these purposes we studied the effect of air contamination by n-heptane (part of automotive fuels) and humidity on ozone production by a dc hollow needle to mesh corona discharge. We found that, for both polarities of the needle electrode, addition of n-heptane to air (a) decreases ozone production; (b) causes discharge poisoning to occur at lower current than for air; (c) does not substantially influence the current for which the ozone production reaches the maximum. Finally the maximum ozone production for the discharge in air occurs for the same current as the maximum ozone production for the discharge contaminated by n-heptane. We also found that humidity decreases ozone production from air contaminated by n-heptane irrespective of the polarity of the coronating needle electrode. This dependence is stronger for the discharge with the needle biased positively

Ozone Production With Dielectric Barrier Discharge: Effects of Power Source and Humidity

KAUST Repository

Zhang, Xuming; Lee, Bok Jik; Im, Hong G.; Cha, Min

2016-01-01

in the production of ozone for the cases of the ac DBD, while increased voltage is more effective for the pulsed DBD. Note that the maximum ozone production efficiency (110 g/kWh) was achieved with the pulsed DBD. At the ED of ∼ 85 J/L, the ozone concentrations

Pulsed Power Production of Ozone in 02/N2 iin a Coaxial Reactor without Dielectric Layer

OpenAIRE

Samaranayake, W. J. M.; Miyahara, Y.; Namihira, T.; Katsuki, S.; Hackam, R.; Akiyama, H.; ミヤハラ, Y.; ナミヒラ, タカオ; カツキ, スナオ; アキヤマ, ヒデノリ; 浪平, 隆男; 勝木, 淳; 秋山, 秀典

2001-01-01

Very short duration pulsed streamer discharges have been used to produce ozone in a gas mixture of nitrogen and oxygen at atmospheric pressure. The ratio of nitrogen to oxygen in the mixture was varied in the range from 2.5/0.5 to 0.5/2.5, while maintaining a total flow rate of 3 l/min. The production of ozone was found to be higher for a specific mixture ratio of N2/O2 than that in oxygen or in dry air. The production of ozone in O2 was higher than that in dry air. The production yield of oz...

Fate and transformation products of amine-terminated PAMAM dendrimers under ozonation and irradiation

International Nuclear Information System (INIS)

Santiago-Morales, Javier; Rosal, Roberto; Hernando, María D.; Ulaszewska, Maria M.; García-Calvo, Eloy; Fernández-Alba, Amadeo R.

2014-01-01

Highlights: • We detected transformation products from dendrimer under ozonation and irradiation. • Retro-Michael fragmentation pathway with highly oxygenated structures. • High toxicity of G3 PAMAM dendrimer for green algae. • Reactive oxygen species were associated with the toxic damage. • Transformation mixtures could be more toxic than the parent dendrimer. -- Abstract: This article deals with the degradation of a third-generation (G3) poly(amidoamine) (PAMAM) dendrimer under ozonation and irradiation. The identification and quantification of G3 PAMAM dendrimer and its transformation products has been performed by liquid chromatography–electrospray ionization-hybrid quadrupole time-of-flight-mass spectrometry. The dendrimer was completely depleted by ozone in less than 1 min. The effect of ultraviolet irradiation was attributed to hydroxyl-mediated oxidation. The transformation products were attributed to the oxidation of amines, which resulted in highly oxidized structures with abundance of carboxylic acids, which started from the formation of amine oxide and the scission of the C-N bond of the amide group. We studied the toxicity of treated mixtures for six different organisms: the acute toxicity for the bacterium Vibrio fischeri and the microcrustacean Daphnia magna, the multigenerational growth inhibition of the alga Pseudokirchneriella subcapitata, and the seed germination phytotoxicity of Licopersicon esculentum, Lactuca sativa and Lolium perenne. Ozonation and irradiation originated transformation products are more toxic than the parent dendrimer. The toxicity of the dendrimer for the green alga was linked to a strong increase of intracellular reactive oxygen species with intense lipid peroxidation

Fate and transformation products of amine-terminated PAMAM dendrimers under ozonation and irradiation

Energy Technology Data Exchange (ETDEWEB)

Santiago-Morales, Javier [Department of Chemical Engineering, University of Alcalá, 28871 Alcalá de Henares, Madrid (Spain); Rosal, Roberto, E-mail: roberto.rosal@uah.es [Department of Chemical Engineering, University of Alcalá, 28871 Alcalá de Henares, Madrid (Spain); Advanced Study Institute of Madrid, IMDEA Agua, Parque Científico Tecnológico, 28805 Alcalá de Henares, Madrid (Spain); Hernando, María D. [Spanish National Institute for Agricultural and Food Research and Technology – INIA, Crta. de la Coruña, km 7.5, 28040 Madrid (Spain); Ulaszewska, Maria M. [Advanced Study Institute of Madrid, IMDEA Agua, Parque Científico Tecnológico, 28805 Alcalá de Henares, Madrid (Spain); García-Calvo, Eloy [Department of Chemical Engineering, University of Alcalá, 28871 Alcalá de Henares, Madrid (Spain); Advanced Study Institute of Madrid, IMDEA Agua, Parque Científico Tecnológico, 28805 Alcalá de Henares, Madrid (Spain); Fernández-Alba, Amadeo R. [Advanced Study Institute of Madrid, IMDEA Agua, Parque Científico Tecnológico, 28805 Alcalá de Henares, Madrid (Spain); Pesticide Residue Research Group, Department of Hydrogeology and Analytical Chemistry, University of Almería, 04120 Almería (Spain)

2014-02-15

Highlights: • We detected transformation products from dendrimer under ozonation and irradiation. • Retro-Michael fragmentation pathway with highly oxygenated structures. • High toxicity of G3 PAMAM dendrimer for green algae. • Reactive oxygen species were associated with the toxic damage. • Transformation mixtures could be more toxic than the parent dendrimer. -- Abstract: This article deals with the degradation of a third-generation (G3) poly(amidoamine) (PAMAM) dendrimer under ozonation and irradiation. The identification and quantification of G3 PAMAM dendrimer and its transformation products has been performed by liquid chromatography–electrospray ionization-hybrid quadrupole time-of-flight-mass spectrometry. The dendrimer was completely depleted by ozone in less than 1 min. The effect of ultraviolet irradiation was attributed to hydroxyl-mediated oxidation. The transformation products were attributed to the oxidation of amines, which resulted in highly oxidized structures with abundance of carboxylic acids, which started from the formation of amine oxide and the scission of the C-N bond of the amide group. We studied the toxicity of treated mixtures for six different organisms: the acute toxicity for the bacterium Vibrio fischeri and the microcrustacean Daphnia magna, the multigenerational growth inhibition of the alga Pseudokirchneriella subcapitata, and the seed germination phytotoxicity of Licopersicon esculentum, Lactuca sativa and Lolium perenne. Ozonation and irradiation originated transformation products are more toxic than the parent dendrimer. The toxicity of the dendrimer for the green alga was linked to a strong increase of intracellular reactive oxygen species with intense lipid peroxidation.

Surface recombination of oxygen atoms in O2 plasma at increased pressure: II. Vibrational temperature and surface production of ozone

Science.gov (United States)

Lopaev, D. V.; Malykhin, E. M.; Zyryanov, S. M.

2011-01-01

Ozone production in an oxygen glow discharge in a quartz tube was studied in the pressure range of 10-50 Torr. The O3 density distribution along the tube diameter was measured by UV absorption spectroscopy, and ozone vibrational temperature TV was found comparing the calculated ab initio absorption spectra with the experimental ones. It has been shown that the O3 production mainly occurs on a tube surface whereas ozone is lost in the tube centre where in contrast the electron and oxygen atom densities are maximal. Two models were used to analyse the obtained results. The first one is a kinetic 1D model for the processes occurring near the tube walls with the participation of the main particles: O(3P), O2, O2(1Δg) and O3 molecules in different vibrational states. The agreement of O3 and O(3P) density profiles and TV calculated in the model with observed ones was reached by varying the single model parameter—ozone production probability (\\gamma_{O_{3}}) on the quartz tube surface on the assumption that O3 production occurs mainly in the surface recombination of physisorbed O(3P) and O2. The phenomenological model of the surface processes with the participation of oxygen atoms and molecules including singlet oxygen molecules was also considered to analyse \\gamma_{O_{3}} data obtained in the kinetic model. A good agreement between the experimental data and the data of both models—the kinetic 1D model and the phenomenological surface model—was obtained in the full range of the studied conditions that allowed consideration of the ozone surface production mechanism in more detail. The important role of singlet oxygen in ozone surface production was shown. The O3 surface production rate directly depends on the density of physisorbed oxygen atoms and molecules and can be high with increasing pressure and energy inputted into plasma while simultaneously keeping the surface temperature low enough. Using the special discharge cell design, such an approach opens up the

Surface recombination of oxygen atoms in O2 plasma at increased pressure: II. Vibrational temperature and surface production of ozone

International Nuclear Information System (INIS)

Lopaev, D V; Malykhin, E M; Zyryanov, S M

2011-01-01

Ozone production in an oxygen glow discharge in a quartz tube was studied in the pressure range of 10-50 Torr. The O 3 density distribution along the tube diameter was measured by UV absorption spectroscopy, and ozone vibrational temperature T V was found comparing the calculated ab initio absorption spectra with the experimental ones. It has been shown that the O 3 production mainly occurs on a tube surface whereas ozone is lost in the tube centre where in contrast the electron and oxygen atom densities are maximal. Two models were used to analyse the obtained results. The first one is a kinetic 1D model for the processes occurring near the tube walls with the participation of the main particles: O( 3 P), O 2 , O 2 ( 1 Δ g ) and O 3 molecules in different vibrational states. The agreement of O 3 and O( 3 P) density profiles and T V calculated in the model with observed ones was reached by varying the single model parameter-ozone production probability (γ O 3 ) on the quartz tube surface on the assumption that O 3 production occurs mainly in the surface recombination of physisorbed O( 3 P) and O 2 . The phenomenological model of the surface processes with the participation of oxygen atoms and molecules including singlet oxygen molecules was also considered to analyse γ O 3 data obtained in the kinetic model. A good agreement between the experimental data and the data of both models-the kinetic 1D model and the phenomenological surface model-was obtained in the full range of the studied conditions that allowed consideration of the ozone surface production mechanism in more detail. The important role of singlet oxygen in ozone surface production was shown. The O 3 surface production rate directly depends on the density of physisorbed oxygen atoms and molecules and can be high with increasing pressure and energy inputted into plasma while simultaneously keeping the surface temperature low enough. Using the special discharge cell design, such an approach opens up

A cloud-ozone data product from Aura OMI and MLS satellite measurements

Directory of Open Access Journals (Sweden)

J. R. Ziemke

2017-11-01

Full Text Available Ozone within deep convective clouds is controlled by several factors involving photochemical reactions and transport. Gas-phase photochemical reactions and heterogeneous surface chemical reactions involving ice, water particles, and aerosols inside the clouds all contribute to the distribution and net production and loss of ozone. Ozone in clouds is also dependent on convective transport that carries low-troposphere/boundary-layer ozone and ozone precursors upward into the clouds. Characterizing ozone in thick clouds is an important step for quantifying relationships of ozone with tropospheric H2O, OH production, and cloud microphysics/transport properties. Although measuring ozone in deep convective clouds from either aircraft or balloon ozonesondes is largely impossible due to extreme meteorological conditions associated with these clouds, it is possible to estimate ozone in thick clouds using backscattered solar UV radiation measured by satellite instruments. Our study combines Aura Ozone Monitoring Instrument (OMI and Microwave Limb Sounder (MLS satellite measurements to generate a new research product of monthly-mean ozone concentrations in deep convective clouds between 30° S and 30° N for October 2004–April 2016. These measurements represent mean ozone concentration primarily in the upper levels of thick clouds and reveal key features of cloud ozone including: persistent low ozone concentrations in the tropical Pacific of  ∼ 10 ppbv or less; concentrations of up to 60 pphv or greater over landmass regions of South America, southern Africa, Australia, and India/east Asia; connections with tropical ENSO events; and intraseasonal/Madden–Julian oscillation variability. Analysis of OMI aerosol measurements suggests a cause and effect relation between boundary-layer pollution and elevated ozone inside thick clouds over landmass regions including southern Africa and India/east Asia.

Ozone production by an atmospheric pulsed discharge with pre-ionization electrodes and partly covered electrode

International Nuclear Information System (INIS)

Kaneda, S.; Shimosaki, M.; Hayashi, N.; Ihara, S.; Satoh, S.; Yamabe, C.

2002-01-01

In this paper, results on ozone production by atmospheric pulsed discharge, are reported. In the research, two types of ozonizer (Type I and Type II) have been used to investigate improvements of ozone concentration and production efficiency. The ozonizer has plane-to-plane metal electrodes structure, and pre-ionization electrodes are placed on the high voltage electrodes (Type I). In Type II, the surface of grounded electrode with 20 mm of width is covered partly by dielectric (thin rubber) with 11 mm of width, while the geometry of both metal electrodes is same to Type I. In the case of Type I, maximum concentration of about 100 ppm and maximum yield of 70 g/kWh were obtained at input power of 0.3 W. On the other hands, in the case of Type II, 800 ppm and 100 g/kWh were obtained at input power of 1.5 W. It was found that the ozone concentration and production yield were improved by using electrode covered by dielectric. (author)

Ozone Production With Dielectric Barrier Discharge: Effects of Power Source and Humidity

KAUST Repository

Zhang, Xuming

2016-08-24

Ozone synthesis in air dielectric barrier discharge (DBD) was studied with an emphasis on the effects of power sources and humidity. Discharge characteristics were investigated to understand the physical properties of plasma and corresponding system performance. It was found that 10-ns pulsed DBD produced a homogeneous discharge mode, while ac DBD yielded an inhomogeneous pattern with many microdischarge channels. At a similar level of the energy density (ED), decreasing the flowrate is more effective in the production of ozone for the cases of the ac DBD, while increased voltage is more effective for the pulsed DBD. Note that the maximum ozone production efficiency (110 g/kWh) was achieved with the pulsed DBD. At the ED of ∼ 85 J/L, the ozone concentrations with dry air were over three times higher than those with the relative humidity of 100% for both the ac DBD and pulsed DBD cases. A numerical simulation was conducted using a global model to understand a detailed chemical role of water vapor to ozone production. It was found HO and OH radicals from water vapor significantly consumed O atoms, resulting in a reduction in ozone production. The global model qualitatively captured the experimental trends, providing further evidence that the primary effect of humidity on ozone production is chemical in nature.

Photocatalytic ozonation of terephthalic acid: a by-product-oriented decomposition study.

Science.gov (United States)

Fuentes, Iliana; Rodríguez, Julia L; Poznyak, Tatyana; Chairez, Isaac

2014-11-01

Terephthalic acid (TA) is considered as a refractory model compound. For this reason, the TA degradation usually requires a prolonged reaction time to achieve mineralization. In this study, vanadium oxide (VxOy) supported on titanium oxide (TiO2) served as a photocatalyst in the ozonation of the TA with light-emitting diodes (LEDs), having a bandwidth centered at 452 nm. The modified catalyst (VxOy/TiO2) in combination with ozone and LEDs improved the TA degradation and its by-products. The results obtained by this system were compared with photolysis, single ozonation, catalytic ozonation, and photocatalytic ozonation of VxOy/TiO2 with UV lamp. The LED-based photocatalytic ozonation showed almost the same decomposition efficiency of the TA, but it was better in comparison with the use of UV lamp. The oxalic acid accumulation, as the final product of the TA decomposition, was directly influenced by either the presence of VxOy or/and the LED irradiation. Several by-products formed during the TA degradation, such as muconic, fumaric, and oxalic acids, were identified. Besides, two unidentified by-products were completely removed during the observed time (60 min). It was proposed that the TA elimination in the presence of VxOy/TiO2 as catalyst was carried out by the combination of different mechanisms: molecular ozone reaction, indirect mechanism conducted by ·OH, and the surface complex formation.

Diurnal variations in H{sub 2}O{sub 2}, O{sub 3}, PAN, HNO{sub 3} and aldehyde concentrations and NO/NO{sub 2} ratios at Rishiri Island, Japan: Potential influence from iodine chemistry

Energy Technology Data Exchange (ETDEWEB)

Kanaya, Yugo [Frontier Research Center for Global Change, Japan Agency for Marine-Earth Science and Technology, 3173-25 Showa-machi, Kanazawa-ku, Yokohama, Kanagawa 236-0001 (Japan)]. E-mail: yugo@jamstec.go.jp; Tanimoto, Hiroshi [National Institute for Environmental Studies, Tsukuba (Japan); Matsumoto, Jun [Integrated Research Institute, Tokyo Institute of Technology, Yokohama (Japan); Furutani, Hiroshi [Department of Chemistry and Biochemistry, University of California, San Diego (United States); Hashimoto, Shigeru [National Institute for Environmental Studies, Tsukuba (Japan); Komazaki, Yuichi [Frontier Research Center for Global Change, Japan Agency for Marine-Earth Science and Technology, 3173-25 Showa-machi, Kanazawa-ku, Yokohama, Kanagawa 236-0001 (Japan); Tanaka, Shigeru [Department of Applied Chemistry, Keio University, Yokohama (Japan); Yokouchi, Yoko [National Institute for Environmental Studies, Tsukuba (Japan); Kato, Shungo [Department of Applied Chemistry, Graduate School of Engineering, Tokyo Metropolitan University, Hachioji (Japan); Kajii, Yoshizumi [Department of Applied Chemistry, Graduate School of Engineering, Tokyo Metropolitan University, Hachioji (Japan); Akimoto, Hajime [Frontier Research Center for Global Change, Japan Agency for Marine-Earth Science and Technology, 3173-25 Showa-machi, Kanazawa-ku, Yokohama, Kanagawa 236-0001 (Japan)

2007-04-15

The presence of iodine chemistry, hypothesized due to the overprediction of HO{sub 2} levels by a photochemical box model at Rishiri Island in June 2000, was quantitatively tested against the observed NO/NO{sub 2} ratios and the net production rates of ozone. The observed NO/NO{sub 2} ratios were reproduced reasonably well by considering the conversion of NO to NO{sub 2} by IO, whose amount was calculated so as to reproduce the observed HO{sub 2} levels. However, the net production rates of ozone were calculated to be negative when such high mixing ratios of IO were considered, which was inconsistent with the observed buildup of ozone during daytime. These results suggest that iodine chemistry may not be the sole mechanism for the reduced mixing ratios of HO{sub 2}, or that 'hot spots' for iodine chemistry were present. Diurnal variations in the mixing ratios of HCHO, CH{sub 3}CHO, peroxy acetyl nitrate (PAN) and HNO{sub 3} observed during the study are presented along with the simulated ones. The box model simulations suggest that the effect of iodine chemistry on these concentrations is small and that important sources of CH{sub 3}CHO and sinks of PAN are probably missing from our current understanding of the tropospheric chemistry mechanism.

Ozone flux over a Norway spruce forest and correlation with net ecosystem production

Czech Academy of Sciences Publication Activity Database

Zapletal, M.; Cudlín, Pavel; Chroust, P.; Urban, Otmar; Pokorný, Radek; Edwards, Magda; Czerný, Radek; Janouš, Dalibor; Taufarová, Klára; Večeřa, Zbyněk; Mikuška, Pavel; Paoletti, E.

2011-01-01

Roč. 159, č. 5 (2011), s. 1024-1034 ISSN 0269-7491 R&D Projects: GA MŽP SP/1B7/189/07 Institutional research plan: CEZ:AV0Z60870520; CEZ:AV0Z40310501 Keywords : ozone deposition * stomatal conductance * deposition velocity * friction velocity * gradient method * tropospheric ozone * net ecosystem production Subject RIV: EH - Ecology, Behaviour Impact factor: 3.746, year: 2011

Intercomparison of ground-based ozone and NO2 measurements during the MANTRA 2004 campaign

Directory of Open Access Journals (Sweden)

K. Strong

2007-11-01

Full Text Available The MANTRA (Middle Atmosphere Nitrogen TRend Assessment 2004 campaign took place in Vanscoy, Saskatchewan, Canada (52° N, 107° W from 3 August to 15 September, 2004. In support of the main balloon launch, a suite of five zenith-sky and direct-Sun-viewing UV-visible ground-based spectrometers was deployed, primarily measuring ozone and NO2 total columns. Three Fourier transform spectrometers (FTSs that were part of the balloon payload also performed ground-based measurements of several species, including ozone. Ground-based measurements of ozone and NO2 differential slant column densities from the zenith-viewing UV-visible instruments are presented herein. They are found to partially agree within NDACC (Network for the Detection of Atmospheric Composition Change standards for instruments certified for process studies and satellite validation. Vertical column densities of ozone from the zenith-sky UV-visible instruments, the FTSs, a Brewer spectrophotometer, and ozonesondes are compared, and found to agree within the combined error estimates of the instruments (15%. NO2 vertical column densities from two of the UV-visible instruments are compared, and are also found to agree within combined error (15%.

Simultaneous waste activated sludge disintegration and biological hydrogen production using an ozone/ultrasound pretreatment.

Science.gov (United States)

Yang, Shan-Shan; Guo, Wan-Qian; Cao, Guang-Li; Zheng, He-Shan; Ren, Nan-Qi

2012-11-01

This paper offers an effective pretreatment method that can simultaneously achieve excess sludge reduction and bio-hydrogen production from sludge self-fermentation. Batch tests demonstrated that the combinative use of ozone/ultrasound pretreatment had an advantage over the individual ozone and ultrasound pretreatments. The optimal condition (ozone dose of 0.158 g O(3)/g DS and ultrasound energy density of 1.423 W/mL) was recommended by response surface methodology. The maximum hydrogen yield was achieved at 9.28 mL H(2)/g DS under the optimal condition. According to the kinetic analysis, the highest hydrogen production rate (1.84 mL/h) was also obtained using combined pretreatment, which well fitted the predicted equation (the squared regression statistic was 0.9969). The disintegration degrees (DD) were limited to 19.57% and 46.10% in individual ozone and ultrasound pretreatments, while it reached up to 60.88% in combined pretreatment. The combined ozone/ultrasound pretreatment provides an ideal and environmental friendly solution to the problem of sludge disposal. Copyright © 2012 Elsevier Ltd. All rights reserved.

Secondary organic aerosol from ozone-initiated reactions with terpene-rich household products

Energy Technology Data Exchange (ETDEWEB)

Coleman, Beverly; Coleman, Beverly K.; Lunden, Melissa M.; Destaillats, Hugo; Nazaroff, William W.

2008-01-01

We analyzed secondary organic aerosol (SOA) data from a series of small-chamber experiments in which terpene-rich vapors from household products were combined with ozone under conditions analogous to product use indoors. Reagents were introduced into a continuously ventilated 198 L chamber at steady rates. Consistently, at the time of ozone introduction, nucleation occurred exhibiting behavior similar to atmospheric events. The initial nucleation burst and growth was followed by a period in which approximately stable particle levels were established reflecting a balance between new particle formation, condensational growth, and removal by ventilation. Airborne particles were measured with a scanning mobility particle sizer (SMPS, 10 to 400 nm) in every experiment and with an optical particle counter (OPC, 0.1 to 2.0 ?m) in a subset. Parameters for a three-mode lognormal fit to the size distribution at steady state were determined for each experiment. Increasing the supply ozone level increased the steady-state mass concentration and yield of SOA from each product tested. Decreasing the air-exchange rate increased the yield. The steady-state fine-particle mass concentration (PM1.1) ranged from 10 to> 300 mu g m-3 and yields ranged from 5percent to 37percent. Steady-state nucleation rates and SOA mass formation rates were on the order of 10 cm-3 s-1 and 10 mu g m-3 min-1, respectively.

Percutaneous intradiscal ozone (O3)-injection: an experimental study in canines

International Nuclear Information System (INIS)

Yu Zhijian; He Xiaofeng; Chen Yong; Zeng Qingle; Liu Chihong; Zhao Zhongqing; Lu Yong; Li Yanhao

2002-01-01

Objective: To evaluate the influence of ozone on normal nucleus pulpous and the safety of intradiscal ozone-injection for the treatment of herniated lumbar disc. Methods: Ozone was injected into selected lumbar discs (3 ml) and the para-spinal space (7 ml) with 20 G Chiba needle under fluoroscopy in five canines. The ozone concentration was 30 μg/ml and 50 μg/ml respectively. Two discs were selected for each concentration. Total 20 discs were injected. Three of the canines were given one-time ozone-injection and were sacrificed for pathology one week, one month and two months respectively after the procedure, and the other two canines were given two-time ozone-injection and were sacrificed one month and two months respectively after the procedure. The specimens including nucleus pulpous, end-plate, spinal cord, nerve root, and greater psoas muscle were observed macroscopically and microscopically. Results: No serious behavior abnormalities were observed in all animals. The atrophy of nucleus pulpous could be observed one month after ozone-injection due to significant reduction of water and extensive proliferation of collagenous fiber. The influence on the atrophy of nucleus pulpous demonstrated no apparent difference between the selected two concentrations of ozone, but was more apparent with two-time injection than that with one-time injection. The end-plates increased slightly or moderately in thickness in 16 simples and a few of fibers in greater psoas muscle suffered slight atrophy in 5 samples. Conclusion: It is suggested that percutaneous intradiscal ozone-injection is a safe method, and can cause gradual atrophy of nucleus pulpous. This study provides the evidence of the feasibility and value of this procedure's application in clinics

Simulation of Halocarbon Production and Emissions and Effects on Ozone Depletion

Science.gov (United States)

Holmes; Ellis

1997-09-01

/ This paper describes an integrated model that simulates future halocarbon production/emissions and potential ozone depletion. Applications and historical production levels for various halocarbons are discussed first. A framework is then presented for modeling future halocarbon impacts incorporating differences in underlying demands, applications, regulatory mandates, and environmental characteristics. The model is used to simulate the potential impacts of several prominent issues relating to halocarbon production, regulation, and environmental interactions, notably: changes in agricultural methyl bromide use, increases in effectiveness of bromine for ozone depletion, modifications to the elimination schedule for HCFCs, short-term expansion of CFC demand in low use compliance countries, and delays in Russian Federation compliance. Individually, each issue does not unequivocally represent a significant likely increase in long-term atmospheric halogen loading and stratospheric ozone depletion. In combination, however, these impacts could increase peak halogen concentrations and long-term integral halogen loading, resulting in higher levels of stratospheric ozone depletion and longer exposure to increased levels of UV radiation.KEY WORDS: Halocarbons; Ozone depletion; Montreal Protocol; Integrated assessment

Investigation of In-Package Ozonation: The Effectiveness of Ozone to Inactive Salmonella enteritidis on Raw, Shell Eggs

Directory of Open Access Journals (Sweden)

Austin Donner

2011-01-01

Full Text Available Food production, handling, and distribution practices pose a constant threat to the quality and safety of food products. The objective of this research is to evaluate an innovative in-package ozonation process to reduce Salmonella enteritidis on raw, shell eggs. Previous research has shown that in-package ozonation eliminates contaminants from outside sources, reduces pathogens, and extends shelf life. In this study, raw, shell eggs were inoculated with Salmonella enteritidis and exposed to ozonation treatment. Microbial recoveries were then tested to determine bacterial reductions. Measurements included: relative humidity (34 percent at 5oC, surface temperatures (oC, ozone concentrations, bacterial reductions of Salmonella enteritidis, and quality assessment of eggs (Haugh Unit [HU], color, pH, and weight. After a 24-hour storage period, all treated samples indicated 3 log10 reductions on average (previous research has achieved up to 6log10. These results show effective in-package ozonation treatment reducing Salmonella enteritidis on raw, shell eggs without significant effect on measured egg quality over time. Benefits of in-package ozonation include no heating, low power requirements (less or equal to 50 Watts, short treatment time (seconds to minutes, and adaptability into existing processes. Given its ability to ensure the safety and longevity of food products, this technology has great potential for utilization in the food processing industry.

Low modeled ozone production suggests underestimation of precursor emissions (especially NOx) in Europe

Science.gov (United States)

Oikonomakis, Emmanouil; Aksoyoglu, Sebnem; Ciarelli, Giancarlo; Baltensperger, Urs; Prévôt, André Stephan Henry

2018-02-01

High surface ozone concentrations, which usually occur when photochemical ozone production takes place, pose a great risk to human health and vegetation. Air quality models are often used by policy makers as tools for the development of ozone mitigation strategies. However, the modeled ozone production is often not or not enough evaluated in many ozone modeling studies. The focus of this work is to evaluate the modeled ozone production in Europe indirectly, with the use of the ozone-temperature correlation for the summer of 2010 and to analyze its sensitivity to precursor emissions and meteorology by using the regional air quality model, the Comprehensive Air Quality Model with Extensions (CAMx). The results show that the model significantly underestimates the observed high afternoon surface ozone mixing ratios (≥ 60 ppb) by 10-20 ppb and overestimates the lower ones (degradation of the model performance for the lower ozone mixing ratios. The model performance for ozone-temperature correlation is also better when NOx emissions are doubled. In the Benelux area, however, the third scenario (where both NOx and VOC emissions are increased) leads to a better model performance. Although increasing only the traffic NOx emissions by a factor of 4 gave very similar results to the doubling of all NOx emissions, the first scenario is more consistent with the uncertainties reported by other studies than the latter, suggesting that high uncertainties in NOx emissions might originate mainly from the road-transport sector rather than from other sectors. The impact of meteorology was examined with three sensitivity tests: (i) increased surface temperature by 4 °C, (ii) reduced wind speed by 50 % and (iii) doubled wind speed. The first two scenarios led to a consistent increase in all surface ozone mixing ratios, thus improving the model performance for the high ozone values but significantly degrading it for the low ozone values, while the third scenario had exactly the

Enhanced ozone production in a pulsed dielectric barrier discharge plasma jet with addition of argon to a He-O2 flow gas

Science.gov (United States)

Sands, Brian; Ganguly, Biswa; Scofield, James

2013-09-01

Ozone production in a plasma jet DBD driven with a 20-ns risetime unipolar pulsed voltage can be significantly enhanced using helium as the primary flow gas with an O2 coflow. The overvolted discharge can be sustained with up to a 5% O2 coflow at pulse repetition frequency at 13 kV applied voltage. Ozone production scales with the pulse repetition frequency up to a ``turnover frequency'' that depends on the O2 concentration, total gas flow rate, and applied voltage. For example, peak ozone densities >1016 cm-3 were measured with 3% O2 admixture and discharge current and 777 nm O(5 P) emission, but decreased ozone production and is followed by a transition to a filamentary discharge mode. The addition of argon at concentrations >=5% reduces the channel conductivity and shifts the turnover frequency to higher frequencies. This results in increased ozone production for a given applied voltage and gas flow rate. Time-resolved Ar(1s5) and He(23S1) metastable densities were acquired along with discharge current and ozone density measurements to gain insight into the mechanisms of optimum ozone production.

Identifying the causes of differences in ozone production from the CB05 and CBMIV chemical mechanisms

Directory of Open Access Journals (Sweden)

R. D. Saylor

2012-02-01

Full Text Available An investigation was conducted to identify the mechanistic differences between two versions of the carbon bond gas-phase chemical mechanism (CB05 and CBMIV which consistently lead to larger ground-level ozone concentrations being produced in the CB05 version of the National Air Quality Forecasting Capability (NAQFC modeling system even though the two parallel forecast systems utilize the same meteorology and base emissions and similar initial and boundary conditions. Box models of each of the mechanisms as they are implemented in the NAQFC were created and a set of 12 sensitivity simulations was designed. The sensitivity simulations independently probed the conceptual mechanistic differences between CB05 and CBMIV and were exercised over a 45-scenario simulation suite designed to emulate the wide range of chemical regimes encountered in a continental-scale atmospheric chemistry model. Results of the sensitivity simulations indicate that two sets of reactions that were included in the CB05 mechanism, but which were absent from the CBMIV mechanism, are the primary causes of the greater ozone production in the CB05 version of the NAQFC. One set of reactions recycles the higher organic peroxide species of CB05 (ROOH, resulting in additional photochemically reactive products that act to produce additional ozone in some chemical regimes. The other set of reactions recycles reactive nitrogen from less reactive forms back to NO₂, increasing the effective NO_x concentration of the system. In particular, the organic nitrate species (NTR, which was a terminal product for reactive nitrogen in the CBMIV mechanism, acts as a reservoir species in CB05 to redistribute NO_x from major source areas to potentially NO_x-sensitive areas where additional ozone may be produced in areas remote from direct NO_x sources.

Photochemical ozone production in tropical squall line convection during NASA Global Tropospheric Experiment/Amazon Boundary Layer Experiment 2A

Science.gov (United States)

Pickering, Kenneth E.; Thompson, Anne M.; Tao, Wei-Kuo; Simpson, Joanne; Scala, John R.

1991-01-01

The role of convection was examined in trace gas transport and ozone production in a tropical dry season squall line sampled on August 3, 1985, during NASA Global Tropospheric Experiment/Amazon Boundary Layer Experiment 2A (NASA GTE/ABLE 2A) in Amazonia, Brazil. Two types of analyses were performed. Transient effects within the cloud are examined with a combination of two-dimensional cloud and one-dimensional photochemical modeling. Tracer analyses using the cloud model wind fields yield a series of cross sections of NO(x), CO, and O3 distribution during the lifetime of the cloud; these fields are used in the photochemical model to compute the net rate of O3 production. At noon, when the cloud was mature, the instantaneous ozone production potential in the cloud is between 50 and 60 percent less than in no-cloud conditions due to reduced photolysis and cloud scavenging of radicals. Analysis of cloud inflows and outflows is used to differentiate between air that is undisturbed and air that has been modified by the storm. These profiles are used in the photochemical model to examine the aftereffects of convective redistribution in the 24-hour period following the storm. Total tropospheric column O3 production changed little due to convection because so little NO(x) was available in the lower troposphere. However, the integrated O3 production potential in the 5- to 13-km layer changed from net destruction to net production as a result of the convection. The conditions of the August 3, 1985, event may be typical of the early part of the dry season in Amazonia, when only minimal amounts of pollution from biomass burning have been transported into the region.

The determination and fate of disinfection by-products from ozonation of polluted raw water

International Nuclear Information System (INIS)

Huang, W.-J.; Fang, G.-C.; Wang, C.-C.

2005-01-01

The major disinfection by-products (DBPs) resulting from ozone treatment of polluted surface water were investigated. By-products of either health concern or which may contribute to biological instability of treated drinking water were investigated. The major DBPs were analyzed in two fractions: carbonyl compounds and brominated organic compounds. The natural organic matter (NOM) was also isolated and fractionated from polluted water for subsequent ozonation and DBPs identification under conditions of typical drinking treatment. The main identified carbonyl compounds were low molecular weight carboxylic acids, benzoic compounds, aliphatic aldehydes and odorous aldehydes, respectively. Brominated organics were also found in ozonated water, including bromoform (CHBr 3 ), monobromoacetic acid (MBAA), dibromoacetic acid (DBAA), 2,4-dibromophenol (2,4-DBP) and dibromoacetonitrile (DBAN), respectively. It was also found that the characteristic of organic precursors have significant influences on brominated organic by-products formation. Humic acid demonstrated the highest CHBr 3 , DBAA and 2,4-DBP formations, whereas hydrophilic neutral produced less CHBr 3 and 2,4-DBP than the rest of the organic fractions but produced the highest amount of DBAN. In addition to the other target compounds, a total of 59 different organic compounds were detected by means of gas chromatograph/high-resolution electron-impact mass spectrometry (GC/EI-MS) detection and tentatively identified using mass spectral library searching, mainly aromatics, acids/esters, alcohols, aldehydes, phthalates and amines/amino acids were analyzed. The percentage of elimination or formation levels reached during ozonation is also discussed in this study

Chemical processes related to net ozone tendencies in the free troposphere

Science.gov (United States)

Bozem, Heiko; Butler, Tim M.; Lawrence, Mark G.; Harder, Hartwig; Martinez, Monica; Kubistin, Dagmar; Lelieveld, Jos; Fischer, Horst

2017-09-01

Ozone (O3) is an important atmospheric oxidant, a greenhouse gas, and a hazard to human health and agriculture. Here we describe airborne in situ measurements and model simulations of O3 and its precursors during tropical and extratropical field campaigns over South America and Europe, respectively. Using the measurements, net ozone formation/destruction tendencies are calculated and compared to 3-D chemistry-transport model simulations. In general, observation-based net ozone tendencies are positive in the continental boundary layer and the upper troposphere at altitudes above ˜ 6 km in both environments. On the other hand, in the marine boundary layer and the middle troposphere, from the top of the boundary layer to about 6-8 km altitude, net O3 destruction prevails. The ozone tendencies are controlled by ambient concentrations of nitrogen oxides (NOx). In regions with net ozone destruction the available NOx is below the threshold value at which production and destruction of O3 balance. While threshold NO values increase with altitude, in the upper troposphere NOx concentrations are generally higher due to the integral effect of convective precursor transport from the boundary layer, downward transport from the stratosphere and NOx produced by lightning. Two case studies indicate that in fresh convective outflow of electrified thunderstorms net ozone production is enhanced by a factor 5-6 compared to the undisturbed upper tropospheric background. The chemistry-transport model MATCH-MPIC generally reproduces the pattern of observation-based net ozone tendencies but mostly underestimates the magnitude of the net tendency (for both net ozone production and destruction).

OMI/Aura Ozone(O3) Total Column 1-Orbit L2 Swath 13x24 km V003 (OMTO3) at GES DISC

Data.gov (United States)

National Aeronautics and Space Administration — The Aura Ozone Monitoring Instrument (OMI) Level-2 Total Column Ozone Data Product OMTO3 (Version 003) is available from the NASA Goddard Earth Sciences Data and...

Impacts of ozone on trees and crops

International Nuclear Information System (INIS)

Felzer, B.S.; Cronina, T.; Melillo, J.M.; Reilly, J.M.; Xiaodong, Wang

2007-01-01

In this review article, we explore how surface-level ozone affects trees and crops with special emphasis on consequences for productivity and carbon sequestration. Vegetation exposure to ozone reduces photosynthesis, growth, and other plant functions. Ozone formation in the atmosphere is a product of NO x , which are also a source of nitrogen deposition. Reduced carbon sequestration of temperate forests resulting from ozone is likely offset by increased carbon sequestration from nitrogen fertilization. However, since fertilized crop-lands are generally not nitrogen-limited, capping ozone-polluting substances in the USA, Europe, and China can reduce future crop yield loss substantially. (authors)

Godiva, a European Project for Ozone and Trace Gas Measurements from GOME

Science.gov (United States)

Goede, A. P. H.; Tanzi, C. P.; Aben, I.; Burrows, J. P.; Weber, M.; Perner, D.; Monks, P. S.; Llewellyn-Jones, D.; Corlett, G. K.; Arlander, D. W.; Platt, U.; Wagner, T.; Pfeilsticker, K.; Taalas, P.; Kelder, H.; Piters, A.

GODIVA (GOME Data Interpretation, Validation and Application) is a European Commission project aimed at the improvement of GOME (Global Ozone Monitoring Experiment) data products. Existing data products include global ozone, NO2 columns and (ir)radiances. Advanced data products include O3 profiles, BrO, HCHO and OCIO columns. These data are validated by ground-based and balloon borne instruments. Calibration issues are investigated by in-flight monitoring using several complementary calibration sources, as well as an on-ground replica of the GOME instrument. The results will lead to specification of operational processing of the EUMETSAT ozone Satellite Application Facility as well as implementation of the improved and new GOME data products in the NILU database for use in the European THESEO (Third European Stratospheric Experiment on Ozone) campaign of 1999

Removal of nalidixic acid and its degradation products by an integrated MBR-ozonation system.

Science.gov (United States)

Pollice, A; Laera, G; Cassano, D; Diomede, S; Pinto, A; Lopez, A; Mascolo, G

2012-02-15

Chemical-biological degradation of a widely spread antibacterial (nalidixic acid) was successfully obtained by an integrated membrane bioreactor (MBR)-ozonation process. The composition of the treated solution simulated the wastewater from the production of the target pharmaceutical, featuring high salinity and a relevant concentration of sodium acetate. Aim of treatment integration was to exploit the synergistic effects of chemical oxidation and bioprocesses, by adopting the latter to remove most of the COD and the ozonation biodegradable products. Integration was achieved by placing ozonation in the recirculation stream of the bioreactor effluent. The recirculation flow rate was three-fold the MBR feed, and the performance of the integrated system was compared to the standard polishing configuration (single ozonation step after the MBR). Results showed that the introduction of the ozonation step did not cause relevant drawbacks to both biological and filtration processes. nalidixic acid passed undegraded through the MBR and was completely removed in the ozonation step. Complete degradation of most of the detected ozonation products was better achieved with the integrated MBR-ozonation process than using the sequential treatment configuration, i.e. ozone polishing after MBR, given the same ozone dosage. Copyright © 2011 Elsevier B.V. All rights reserved.

Effects of ozone treatment on Botrytis cinerea and Sclerotinia sclerotiorum in relation to horticultural product quality.

Science.gov (United States)

Sharpe, Deana; Fan, Lihua; McRae, Ken; Walker, Brad; MacKay, Ron; Doucette, Craig

2009-08-01

Botrytis cinerea and Sclerotinia sclerotiorum are fungal pathogens that cause the decay of many fruits and vegetables. Ozone may be used as an antimicrobial agent to control the decay. The effect of gaseous ozone on spore viability of B. cinerea and mycelial growth of B. cinerea and S. sclerotiorum were investigated. Spore viability of B. cinerea was reduced by over 99.5% (P < 0.01) and height of the aerial mycelium was reduced from 4.7 mm in the control to less than 1 mm after exposure to 450 or 600 ppb ozone for 48 h at 20 degrees C. Sporulation of B. cinerea was also substantially inhibited by ozone treatments. However, ozone had no significant effect on mycelial growth of S. sclerotiorum in vitro. Decay and quality parameters including color, chlorophyll fluorescence (CF), and ozone injury were further assessed for various horticultural commodities (apple, grape, highbush blueberry, and carrot) treated with 450 ppb of ozone for 48 h at 20 degrees C over a period of 12 d. Lesion size and height of the aerial mycelium were significantly reduced by the ozone treatment on carrots inoculated with mycelial agar plugs of B. cinerea or S. sclerotiorum. Lesion size was also reduced on treated apples inoculated with 5 x 10(6) spores/mL of B. cinerea, and decay incidence of treated grapes was reduced. The 450 ppb ozone for 48 h treatment had no significant effect on color of carrots and apples or on CF of apples and grapes. Ozone, an environmentally sound antimicrobial agent, inactivates microorganisms through oxidization and residual ozone spontaneously decomposes to nontoxic products. It may be applied to fruits and vegetables to reduce decay and extend shelf life.

Colour removal and carbonyl by-production in high dose ozonation for effluent polishing.

Science.gov (United States)

Mezzanotte, V; Fornaroli, R; Canobbio, S; Zoia, L; Orlandi, M

2013-04-01

Experimental tests have been conducted to investigate the efficiency and the by-product generation of high dose ozonation (10-60 mg O3 L(-1)) for complete colour removal from a treated effluent with an important component of textile dyeing wastewater. The effluent is discharged into an effluent-dominated stream where no dilution takes place, and, thus, the quality requirement for the effluents is particularly strict. 30, 60 and 90 min contact times were adopted. Colour was measured as absorbance at 426, 558 and 660 nm wavelengths. pH was monitored throughout the experiments. The experimental work showed that at 50 mg L(-1) colour removal was complete and at 60 mg O3 L(-1) the final aldehyde concentration ranged between 0.72 and 1.02 mg L(-1). Glyoxal and methylglyoxal concentrations were directly related to colour removal, whereas formaldehyde, acetaldehyde, acetone and acrolein were not. Thus, the extent of colour removal can be used to predict the increase in glyoxal and methylglyoxal concentrations. As colour removal can be assessed by a simple absorbance measurement, in contrast to the analysis of specific carbonyl compounds, which is much longer and complex, the possibility of using colour removal as an indicator for predicting the toxic potential of ozone by-products for textile effluents is of great value. Copyright © 2013 Elsevier Ltd. All rights reserved.

Experimental monitoring of ozone production in a PET cyclotron facility

International Nuclear Information System (INIS)

Zanibellato, L.; Cicoria, G.; Pancaldi, D.; Boschi, S.; Mostacci, D.; Marengo, M.

2010-01-01

Ozone produced from radiolytic processes was investigated as a possible health hazard in the working environment at the University Hospital 'S.Orsola-Malpighi' PET facility. Intense radiation fields can generate ozone, known to be the most toxic gas produced by ionizing radiation around a particle accelerator. To evaluate ozone concentration in air, two different measurement campaigns were conducted with passive diffusion detectors. Comparison of the results with the concentration limits recommended by American Conference of Governmental Industrial Hygienists (ACGIH) demonstrated that ozone poses no health hazard to workers around a biomedical cyclotron.

Ozone production in summer in the megacities of Tianjin and Shanghai, China: a comparative study

Directory of Open Access Journals (Sweden)

L. Ran

2012-08-01

Full Text Available Rapid economic growth has given rise to a significant increase in ozone precursor emissions in many regions of China, especially in the densely populated North China Plain (NCP and Yangtze River Delta (YRD. Improved understanding of ozone formation in response to different precursor emissions is imperative to address the highly nonlinear ozone problem and to provide a solid scientific basis for efficient ozone abatement in these regions. A comparative study on ozone photochemical production in summer has thus been carried out in the megacities of Tianjin (NCP and Shanghai (YRD. Two intensive field campaigns were carried out respectively at an urban and a suburban site of Tianjin, in addition to routine monitoring of trace gases in Shanghai, providing data sets of surface ozone and its precursors including nitrogen oxides (NO_x and various non-methane hydrocarbons (NMHCs. Ozone pollution in summer was found to be more severe in the Tianjin region than in the Shanghai region, based on either the frequency or the duration of high ozone events. Such differences might be attributed to the large amount of highly reactive NMHCs in Tianjin. Industry related species like light alkenes were of particular importance in both urban and suburban Tianjin, while in Shanghai aromatics dominated. In general, the ozone problem in Shanghai is on an urban scale. Stringent control policies on local emissions would help reduce the occurrence of high ozone concentrations. By contrast, ozone pollution in Tianjin is probably a regional problem. Combined efforts to reduce ozone precursor emissions on a regional scale must be undertaken to bring the ozone problem under control.

Trends of Ozone in Switzerland since 1992 (TROZOS)

Energy Technology Data Exchange (ETDEWEB)

Ordonez, C.; Mathis, H.; Furger, M.; Prevot, A.S.H

2004-07-01

This work reports on the trends of the daily afternoon (noon to midnight) maximum ozone concentrations at 15 of the 16 stations of the Swiss air quality monitoring network (NABEL) during the period 1992-2002. The use of numerous meteorological parameters and additional data allowed a detailed seasonal analysis of the influence of the weather on the ozone maxima at the different stations. An analysis of covariance (ANCOVA) was performed separately for each station and season in order to detect the parameters which best explain the variability of the daily ozone maximum concentrations. During the warm seasons (summer and spring) the most explanatory parameters are those related to the ozone production, in particular the afternoon temperature. In winter, the most explanatory variables are the ones influencing the vertical mixing and thus the ozone destruction by titration with NO and dry deposition, like the afternoon global radiation. The trends of both the measured and meteorologically corrected ozone maxima were calculated. The year-to-year variability in the ozone maxima was lowered by a factor of 3 by the meteorological correction. Significantly positive trends of corrected ozone maxima of 0.3 - 1.1 ppb/year were found at the low altitude stations in winter and autumn as well as at Lausanne - urban station - in all the seasons, mainly due to the lower loss of ozone by reaction with NO as a consequence of the decreased emissions of primary pollutants during the 90s. This could be partially confirmed by the lower trends of O{sub X} (sum O{sub 3} of and NO{sub 2}) maxima compared to the trends in ozone maxima. The absence of negative trends of the median or mean ozone maxima north of the Alps in summer suggests that the decrease in the emissions of ozone precursors did not have a strong impact on the afternoon maximum ozone concentrations during the last decade. In contrast to the project TOSS (Trends of Ozone in Southern Switzerland), no significantly negative

Trends of Ozone in Switzerland since 1992 (TROZOS)

International Nuclear Information System (INIS)

Ordonez, C.; Mathis, H.; Furger, M.; Prevot, A.S.H.

2004-07-01

This work reports on the trends of the daily afternoon (noon to midnight) maximum ozone concentrations at 15 of the 16 stations of the Swiss air quality monitoring network (NABEL) during the period 1992-2002. The use of numerous meteorological parameters and additional data allowed a detailed seasonal analysis of the influence of the weather on the ozone maxima at the different stations. An analysis of covariance (ANCOVA) was performed separately for each station and season in order to detect the parameters which best explain the variability of the daily ozone maximum concentrations. During the warm seasons (summer and spring) the most explanatory parameters are those related to the ozone production, in particular the afternoon temperature. In winter, the most explanatory variables are the ones influencing the vertical mixing and thus the ozone destruction by titration with NO and dry deposition, like the afternoon global radiation. The trends of both the measured and meteorologically corrected ozone maxima were calculated. The year-to-year variability in the ozone maxima was lowered by a factor of 3 by the meteorological correction. Significantly positive trends of corrected ozone maxima of 0.3 - 1.1 ppb/year were found at the low altitude stations in winter and autumn as well as at Lausanne - urban station - in all the seasons, mainly due to the lower loss of ozone by reaction with NO as a consequence of the decreased emissions of primary pollutants during the 90s. This could be partially confirmed by the lower trends of O X (sum O 3 of and NO 2 ) maxima compared to the trends in ozone maxima. The absence of negative trends of the median or mean ozone maxima north of the Alps in summer suggests that the decrease in the emissions of ozone precursors did not have a strong impact on the afternoon maximum ozone concentrations during the last decade. In contrast to the project TOSS (Trends of Ozone in Southern Switzerland), no significantly negative trends of ozone

A comparison of chemical mechanisms using tagged ozone production potential (TOPP analysis

Directory of Open Access Journals (Sweden)

J. Coates

2015-08-01

Full Text Available Ground-level ozone is a secondary pollutant produced photochemically from reactions of NOx with peroxy radicals produced during volatile organic compound (VOC degradation. Chemical transport models use simplified representations of this complex gas-phase chemistry to predict O3 levels and inform emission control strategies. Accurate representation of O3 production chemistry is vital for effective prediction. In this study, VOC degradation chemistry in simplified mechanisms is compared to that in the near-explicit Master Chemical Mechanism (MCM using a box model and by "tagging" all organic degradation products over multi-day runs, thus calculating the tagged ozone production potential (TOPP for a selection of VOCs representative of urban air masses. Simplified mechanisms that aggregate VOC degradation products instead of aggregating emitted VOCs produce comparable amounts of O3 from VOC degradation to the MCM. First-day TOPP values are similar across mechanisms for most VOCs, with larger discrepancies arising over the course of the model run. Aromatic and unsaturated aliphatic VOCs have the largest inter-mechanism differences on the first day, while alkanes show largest differences on the second day. Simplified mechanisms break VOCs down into smaller-sized degradation products on the first day faster than the MCM, impacting the total amount of O3 produced on subsequent days due to secondary chemistry.

Dobson spectrophotometer ozone measurements during international ozone rocketsonde intercomparison

Science.gov (United States)

Parsons, C. L.

1980-01-01

Measurements of the total ozone content of the atmosphere, made with seven ground based instruments at a site near Wallops Island, Virginia, are discussed in terms for serving as control values with which the rocketborne sensor data products can be compared. These products are profiles of O3 concentration with altitude. By integrating over the range of altitudes from the surface to the rocket apogee and by appropriately estimating the residual ozone amount from apogee to the top of the atmosphere, a total ozone amount can be computed from the profiles that can be directly compared with the ground based instrumentation results. Dobson spectrophotometers were used for two of the ground-based instruments. Preliminary data collected during the IORI from Dobson spectrophotometers 72 and 38 are presented. The agreement between the two and the variability of total ozone overburden through the experiment period are discussed.

Effect of ozonolysis pretreatment parameters on the sugar release, ozone consumption and ethanol production from sugarcane bagasse.

Science.gov (United States)

Travaini, Rodolfo; Barrado, Enrique; Bolado-Rodríguez, Silvia

2016-08-01

A L9(3)(4) orthogonal array (OA) experimental design was applied to study the four parameters considered most important in the ozonolysis pretreatment (moisture content, ozone concentration, ozone/oxygen flow and particle size) on ethanol production from sugarcane bagasse (SCB). Statistical analysis highlighted ozone concentration as the highest influence parameter on reaction time and sugars release after enzymatic hydrolysis. The increase on reaction time when decreasing the ozone/oxygen flow resulted in small differences of ozone consumptions. Design optimization for sugars release provided a parameters combination close to the best experimental run, where 77.55% and 56.95% of glucose and xylose yields were obtained, respectively. When optimizing the grams of sugar released by gram of ozone, the highest influence parameter was moisture content, with a maximum yield of 2.98gSUGARS/gO3. In experiments on hydrolysates fermentation, Saccharomyces cerevisiae provided ethanol yields around 80%, while Pichia stipitis was completely inhibited. Copyright © 2016 Elsevier Ltd. All rights reserved.

Photochemical production of ozone in Beijing during the 2008 Olympic Games

Science.gov (United States)

Chou, C. C.-K.; Tsai, C.-Y.; Chang, C.-C.; Lin, P.-H.; Liu, S. C.; Zhu, T.

2011-09-01

As a part of the CAREBeijing-2008 campaign, observations of O3, oxides of nitrogen (NOx and NOy), CO, and hydrocarbons (NMHCs) were carried out at the air quality observatory of the Peking University in Beijing, China during August 2008, including the period of the 29th Summer Olympic Games. The measurements were compared with those of the CAREBeijing-2006 campaign to evaluate the effectiveness of the air pollution control measures, which were conducted for improving the air quality in Beijing during the Olympics. The results indicate that significant reduction in the emissions of primary air pollutants had been achieved; the monthly averaged mixing ratios of NOx, NOy, CO, and NMHCs decreased by 42.2, 56.5, 27.8, and 49.7 %, respectively. In contrast to the primary pollutants, the averaged mixing ratio of O3 increased by 42.2 %. Nevertheless, it was revealed that the ambient levels of total oxidant (Ox = O3+NO2+1.5 NOz) and NOz were reduced by 21.3 and 77.4 %, respectively. The contradictions between O3 and Ox were further examined in two case studies. Ozone production rates of 30-70 ppbv h-1 and OPEx of ~8 mole mole-1 were observed on a clear-sky day in spite of the reduced levels of precursors. In that case, it was found that the mixing ratio of O3 increased with the increasing NO2/NO ratio, whereas the NOz mixing ratio leveled off when NO2/NO>8. Consequently, the ratio of O3 to NOz increased to above 10, indicating the shift from VOC-sensitive regime to NOx-sensitive regime. However, in the other case, it was found that the O3 production was inhibited significantly due to substantial reduction in the NMHCs. According to the observations, it was suggested that the O3 and/or Ox production rates in Beijing should have been reduced as a result of the reduction in the emissions of precursors during the Olympic period. However, the nighttime O3 levels increased due to a decline in the NO-O3 titration, and the midday O3 peak levels were elevated because of the shift in

Particulate matter air pollution may offset ozone damage to global crop production

Science.gov (United States)

Schiferl, Luke D.; Heald, Colette L.

2018-04-01

Ensuring global food security requires a comprehensive understanding of environmental pressures on food production, including the impacts of air quality. Surface ozone damages plants and decreases crop production; this effect has been extensively studied. In contrast, the presence of particulate matter (PM) in the atmosphere can be beneficial to crops given that enhanced light scattering leads to a more even and efficient distribution of photons which can outweigh total incoming radiation loss. This study quantifies the impacts of ozone and PM on the global production of maize, rice, and wheat in 2010 and 2050. We show that accounting for the growing season of these crops is an important factor in determining their air pollution exposure. We find that the effect of PM can offset much, if not all, of the reduction in yield associated with ozone damage. Assuming maximum sensitivity to PM, the current (2010) global net impact of air quality on crop production varies by crop (+5.6, -3.7, and +4.5 % for maize, wheat, and rice, respectively). Future emissions scenarios indicate that attempts to improve air quality can result in a net negative effect on crop production in areas dominated by the PM effect. However, we caution that the uncertainty in this assessment is large, due to the uncertainty associated with crop response to changes in diffuse radiation; this highlights that a more detailed physiological study of this response for common cultivars is crucial.

Particulate matter air pollution may offset ozone damage to global crop production

Directory of Open Access Journals (Sweden)

L. D. Schiferl

2018-04-01

Full Text Available Ensuring global food security requires a comprehensive understanding of environmental pressures on food production, including the impacts of air quality. Surface ozone damages plants and decreases crop production; this effect has been extensively studied. In contrast, the presence of particulate matter (PM in the atmosphere can be beneficial to crops given that enhanced light scattering leads to a more even and efficient distribution of photons which can outweigh total incoming radiation loss. This study quantifies the impacts of ozone and PM on the global production of maize, rice, and wheat in 2010 and 2050. We show that accounting for the growing season of these crops is an important factor in determining their air pollution exposure. We find that the effect of PM can offset much, if not all, of the reduction in yield associated with ozone damage. Assuming maximum sensitivity to PM, the current (2010 global net impact of air quality on crop production varies by crop (+5.6, −3.7, and +4.5 % for maize, wheat, and rice, respectively. Future emissions scenarios indicate that attempts to improve air quality can result in a net negative effect on crop production in areas dominated by the PM effect. However, we caution that the uncertainty in this assessment is large, due to the uncertainty associated with crop response to changes in diffuse radiation; this highlights that a more detailed physiological study of this response for common cultivars is crucial.

Field observations of regional and urban impacts on NO2, ozone, UVB, and nitrate radical production rates in the Phoenix air basin

International Nuclear Information System (INIS)

Gaffney, J.S.; Marley, N.A.; Drayton, P.J.; Doskey, P.V.; Kotamarthi, V.R.; Cunningham, M.M.; Baird, J.C.; Dintaman, J.; Hart, H.L.

2002-01-01

In the May and June of 1998, field measurements were taken at a site near the Usery Pass Recreation Area, ∼27 miles from the downtown Phoenix area, overlooking Phoenix and Mesa, Arizona. This site was selected to examine the impacts of the Phoenix urban plume on the Usery Pass Recreation Area and surrounding regions. Data were obtained for ultraviolet-B (UVB) radiation, nitrogen dioxide (NO 2 ), peroxyacetyl nitrate (PAN), ozone (O 3 ), and carbon monoxide (CO). Nocturnal plumes of NO 2 (in tens of ppb), observed near midnight, were correlated with CO and anti-correlated with O 3 . This behavior was consistent with the titration of locally generated NO by boundary layer O 3 to form the nighttime NO 2 plumes that were subsequently transported into the Usery Pass Recreation area. Nitrate radical (NO 3 ) production rates were calculated to be very high on the edges of these nocturnal plumes. Examination of O 3 and PAN data also indicates that Phoenix is being affected by long-range transport of pollutants from the Los Angeles to San Diego areas. A regional smoke episode was observed in May, accompanied by a decrease in UVB of factor of two and a decrease in O 3 and an increase in methyl chloride. Low level back trajectories and chemical evidence confirm that the smoke event originated in northern Mexico and that the reduced O 3 levels observed at Usery Pass could be partially due to reduced photolysis rates caused by carbonaceous soot aerosols transported in the smoke plume. The results are discussed with regard to potential effects of local pollution transport from the Phoenix air basin as well as an assessment of the contributions from long-range transport of pollutants to the background levels in the Phoenix-Usery Pass area. (author)

Effect of operational and water quality parameters on conventional ozonation and the advanced oxidation process O3/H2O2: Kinetics of micropollutant abatement, transformation product and bromate formation in a surface water.

Science.gov (United States)

Bourgin, Marc; Borowska, Ewa; Helbing, Jakob; Hollender, Juliane; Kaiser, Hans-Peter; Kienle, Cornelia; McArdell, Christa S; Simon, Eszter; von Gunten, Urs

2017-10-01

The efficiency of ozone-based processes under various conditions was studied for the treatment of a surface water (Lake Zürich water, Switzerland) spiked with 19 micropollutants (pharmaceuticals, pesticides, industrial chemical, X-ray contrast medium, sweetener) each at 1 μg L -1 . Two pilot-scale ozonation reactors (4-5 m 3  h -1 ), a 4-chamber reactor and a tubular reactor, were investigated by either conventional ozonation and/or the advanced oxidation process (AOP) O 3 /H 2 O 2 . The effects of selected operational parameters, such as ozone dose (0.5-3 mg L -1 ) and H 2 O 2 dose (O 3 :H 2 O 2  = 1:3-3:1 (mass ratio)), and selected water quality parameters, such as pH (6.5-8.5) and initial bromide concentration (15-200 μg L -1 ), on micropollutant abatement and bromate formation were investigated. Under the studied conditions, compounds with high second-order rate constants k O3 >10 4  M -1  s -1 for their reaction with ozone were well abated (>90%) even for the lowest ozone dose of 0.5 mg L -1 . Conversely, the abatement efficiency of sucralose, which only reacts with hydroxyl radicals (OH), varied between 19 and 90%. Generally, the abatement efficiency increased with higher ozone doses and higher pH and lower bromide concentrations. H 2 O 2 addition accelerated the ozone conversion to OH, which enables a faster abatement of ozone-resistant micropollutants. Interestingly, the abatement of micropollutants decreased with higher bromide concentrations during conventional ozonation due to competitive ozone-consuming reactions, except for lamotrigine, due to the suspected reaction of HOBr/OBr - with the primary amine moieties. In addition to the abatement of micropollutants, the evolution of the two main transformation products (TPs) of hydrochlorothiazide (HCTZ) and tramadol (TRA), chlorothiazide (CTZ) and tramadol N-oxide (TRA-NOX), respectively, was assessed by chemical analysis and kinetic modeling. Both selected TPs were quickly formed initially

Kinetics of the degradation of 2-chlorophenol by ozonation at pH 3

International Nuclear Information System (INIS)

Sung Menghau; Huang, C.P.

2007-01-01

Prediction of byproduct distribution during ozonation is of importance to the design of treatment process. In this study, degradation products in direct ozonation of 2-chlorophenol in aqueous solution were identified by employing the chemical derivatization technique, specifically, silylation. Transient distribution of degradation products, in a semi-batch reactor under three ozone dosages were identified and determined by HPLC analysis. An empirical degradation pathway was proposed to describe the ozonation reaction. A mathematical protocol consisting of 11 equations and 12 rate constants was developed to solve and optimize the kinetic parameters. Modeling results revealed that the empirical pathway was capable of predicting the ozonation reaction at the beginning phase under a higher ozone dosage (e.g., greater than 6 mg/L g ). The degree of agreement between predicted and experimental data decreased as the ozone dosage decreased to 1.2 mg/L g . Results suggested that there was a dosage-dependent pathway in the direct ozonation of 2-chlorophenol

Rapid increases in tropospheric ozone production and export from China

NARCIS (Netherlands)

Verstraeten, W.W.; Neu, J.L.; Williams, J.E.; Bowman, K.W.; Worden, J.R.; Boersma, K.F.

2015-01-01

Rapid population growth and industrialization have driven substantial increases in Asian ozone precursor emissions over the past decade1, with highly uncertain impacts on regional and global tropospheric ozone levels. According to ozonesonde measurements2, 3, tropospheric ozone concentrations at two

Transformation products and reaction kinetics of fragrances in advanced wastewater treatment with ozone

DEFF Research Database (Denmark)

Janzen, Niklas; Dopp, Elke; Hesse, Julia

2011-01-01

) ethanone (musk ketone/MK), and 1-(2,3,8,8-tetramethyl-1,3,4,5,6,7-hexahydronaphthalen-2-yl)ethanone (OTNE) with ozone in tap water as well as waste water treatment plant (WWTP) effluents is described. Several transformation products are characterized by means of gas chromatography coupled to mass...

Limonene and its ozone-initiated reaction products attenuate allergic lung inflammation in mice.

Science.gov (United States)

Hansen, Jitka S; Nørgaard, Asger W; Koponen, Ismo K; Sørli, Jorid B; Paidi, Maya D; Hansen, Søren W K; Clausen, Per Axel; Nielsen, Gunnar D; Wolkoff, Peder; Larsen, Søren Thor

2016-11-01

Inhalation of indoor air pollutants may cause airway irritation and inflammation and is suspected to worsen allergic reactions. Inflammation may be due to mucosal damage, upper (sensory) and lower (pulmonary) airway irritation due to activation of the trigeminal and vagal nerves, respectively, and to neurogenic inflammation. The terpene, d-limonene, is used as a fragrance in numerous consumer products. When limonene reacts with the pulmonary irritant ozone, a complex mixture of gas and particle phase products is formed, which causes sensory irritation. This study investigated whether limonene, ozone or the reaction mixture can exacerbate allergic lung inflammation and whether airway irritation is enhanced in allergic BALB/cJ mice. Naïve and allergic (ovalbumin sensitized) mice were exposed via inhalation for three consecutive days to clean air, ozone, limonene or an ozone-limonene reaction mixture. Sensory and pulmonary irritation was investigated in addition to ovalbumin-specific antibodies, inflammatory cells, total protein and surfactant protein D in bronchoalveolar lavage fluid and hemeoxygenase-1 and cytokines in lung tissue. Overall, airway allergy was not exacerbated by any of the exposures. In contrast, it was found that limonene and the ozone-limonene reaction mixture reduced allergic inflammation possibly due to antioxidant properties. Ozone induced sensory irritation in both naïve and allergic mice. However, allergic but not naïve mice were protected from pulmonary irritation induced by ozone. This study showed that irritation responses might be modulated by airway allergy. However, aggravation of allergic symptoms was observed by neither exposure to ozone nor exposure to ozone-initiated limonene reaction products. In contrast, anti-inflammatory properties of the tested limonene-containing pollutants might attenuate airway allergy.

Ozone oxidation of antidepressants in wastewater –Treatment evaluation and characterization of new by-products by LC-QToFMS

Directory of Open Access Journals (Sweden)

Lajeunesse André

2013-01-01

Full Text Available Abstract Background The fate of 14 antidepressants along with their respective N-desmethyl metabolites and the anticonvulsive drug carbamazepine was examined in a primary sewage treatment plant (STP and following advanced treatments with ozone (O3. The concentrations of each pharmaceutical compound were determined in raw sewage, effluent and sewage sludge samples by LC-MS/MS analysis. The occurrence of antidepressant by-products formed in treated effluent after ozonation was also investigated. Results Current primary treatments using physical and chemical processes removed little of the compounds (mean removal efficiency: 19%. Experimental sorption coefficients (Kd of each studied compounds were also calculated. Sorption of venlafaxine, desmethylvenlafaxine, and carbamazepine on sludge was assumed to be negligible (log Kd ≤ 2, but higher sorption behavior can be expected for sertraline (log Kd ≥ 4. Ozonation treatment with O3 (5 mg/L led to a satisfactory mean removal efficiency of 88% of the compounds. Screening of the final ozone-treated effluent samples by high resolution-mass spectrometry (LC-QqToFMS did confirm the presence of related N-oxide by-products. Conclusion Effluent ozonation led to higher mean removal efficiencies than current primary treatment, and therefore represented a promising strategy for the elimination of antidepressants in urban wastewaters. However, the use of O3 produced by-products with unknown toxicity.

Products and mechanisms of the reaction of gas phase ozone with organic colorants

Energy Technology Data Exchange (ETDEWEB)

Grosjean, D. (DGA, Inc., Ventura, CA (USA)); Druzik, J.R. (Getty Conservation Institute, Marina del Rey, CA (USA)); Sensharma, D.K. (Univ. of California, Los Angeles (USA)); Whitmore, P.M.; DeMoor, C.P.; Cass, G.R. (California Institute of Technology, Pasadena (USA))

1988-09-01

Studies carried out in this laboratory have shown that many artists organic colorants fade substantially when exposed to ozone in the dark. These studies typically involved pigment exposure for 12 weeks to purified air containing 0.3-0.4 ppm of ozone at ambient temperature and humidity. These laboratory conditions are equivalent to about six years of exposure inside a typical air-conditioned building in Los Angeles, and the observed fading is therefore directly relevant to possible damage to works of arts in museum settings. Organic colorants that were most ozone-fugitive included natural colorants, such as curcumin and indigo, as well as modern synthetic colorants such as alizarin lakes and triphenylmethane dyes. Thus, these colorants were selected for further study with emphasis on the nature of the reaction products. Exposures were carried out on different substrates including watercolor paper, cellulose, silica gel, and Teflon. The experiments involved long-term exposure to low levels of ozone (e.g. {approximately} 0.3 ppm for 90 days) or shorter-term exposure to higher ozone concentrations (e.g. 10 ppm for 24 hours). Exposed and control samples, along with solvent and substrate blanks, were analyzed by mass spectrometry using a Kratos Scientific Instruments MS25 hexapole mass spectrometer operated in either methane chemical ionization (CI) or electron impact (EI) modes.

Application of ozonation for pharmaceuticals and personal care products removal from water.

Science.gov (United States)

Gomes, João; Costa, Raquel; Quinta-Ferreira, Rosa M; Martins, Rui C

2017-05-15

Due to the shortening on natural water resources, reclaimed wastewater will be an important water supply source. However, suitable technologies must be available to guaranty its proper detoxification with special concern for the emerging pharmaceutical and personal care products that are continuously reaching municipal wastewater treatment plants. While conventional biological systems are not suitable to remove these compounds, ozone, due to its interesting features involving molecular ozone oxidation and the possibility of generating unselective hydroxyl radicals, has a wider range of action on micropollutants removal and water disinfection. This paper aims to review the studies dealing with ozone based processes for water reuse by considering municipal wastewater reclamation as well as natural and drinking water treatment. A comparison with alternative technologies is given. The main drawback of ozonation is related with the low mineralization achieved that may lead to the production of reaction intermediates with toxic features. The use of hydrogen peroxide and light aided systems enhance ozone action over pollutants. Moreover, scientific community is focused on the development of solid catalysts able to improve the mineralization level achieved by ozone. Special interest is now being given to solar light catalytic ozonation systems with interesting results both for chemical and biological contaminants abatement. Nowadays the integration between ozonation and sand biofiltration seems to be the most interesting cost effective methodology for water treatment. However, further studies must be performed to optimize this system by understanding the biofiltration mechanisms. Copyright © 2017 Elsevier B.V. All rights reserved.

Regulation of ozone-induced lung inflammation and injury by the β-galactoside-binding lectin galectin-3

International Nuclear Information System (INIS)

Sunil, Vasanthi R.; Francis, Mary; Vayas, Kinal N.; Cervelli, Jessica A.; Choi, Hyejeong; Laskin, Jeffrey D.; Laskin, Debra L.

2015-01-01

Macrophages play a dual role in ozone toxicity, contributing to both pro- and anti-inflammatory processes. Galectin-3 (Gal-3) is a lectin known to regulate macrophage activity. Herein, we analyzed the role of Gal-3 in the response of lung macrophages to ozone. Bronchoalveolar lavage (BAL) and lung tissue were collected 24–72 h after exposure (3 h) of WT and Gal-3 -/- mice to air or 0.8 ppm ozone. In WT mice, ozone inhalation resulted in increased numbers of proinflammatory (Gal-3 + , iNOS + ) and anti-inflammatory (MR-1 + ) macrophages in the lungs. While accumulation of iNOS + macrophages was attenuated in Gal-3 -/- mice, increased numbers of enlarged MR-1 + macrophages were noted. This correlated with increased numbers of macrophages in BAL. Flow cytometric analysis showed that these cells were CD11b + and consisted mainly (> 97%) of mature (F4/80 + CD11c + ) proinflammatory (Ly6GLy6C hi ) and anti-inflammatory (Ly6GLy6C lo ) macrophages. Increases in both macrophage subpopulations were observed following ozone inhalation. Loss of Gal-3 resulted in a decrease in Ly6C hi macrophages, with no effect on Ly6C lo macrophages. CD11b + Ly6G + Ly6C + granulocytic (G) and monocytic (M) myeloid derived suppressor cells (MDSC) were also identified in the lung after ozone. In Gal-3 -/- mice, the response of G-MDSC to ozone was attenuated, while the response of M-MDSC was heightened. Changes in inflammatory cell populations in the lung of ozone treated Gal-3 -/- mice were correlated with reduced tissue injury as measured by cytochrome b5 expression. These data demonstrate that Gal-3 plays a role in promoting proinflammatory macrophage accumulation and toxicity in the lung following ozone exposure. - Highlights: • Multiple monocytic-macrophage subpopulations accumulate in the lung after ozone inhalation. • Galectin-3 plays a proinflammatory role in ozone-induced lung injury. • In the absence of gal-3, inflammatory cells with a myeloid derived suppressor cell phenotype

Effects of conventional ozonation and electro-peroxone pretreatment of surface water on disinfection by-product formation during subsequent chlorination.

Science.gov (United States)

Mao, Yuqin; Guo, Di; Yao, Weikun; Wang, Xiaomao; Yang, Hongwei; Xie, Yuefeng F; Komarneni, Sridhar; Yu, Gang; Wang, Yujue

2018-03-01

The electro-peroxone (E-peroxone) process is an emerging ozone-based electrochemical advanced oxidation process that combines conventional ozonation with in-situ cathodic hydrogen peroxide (H 2 O 2 ) production for oxidative water treatment. In this study, the effects of the E-peroxone pretreatment on disinfection by-product (DBP) formation from chlorination of a synthetic surface water were investigated and compared to conventional ozonation. Results show that due to the enhanced transformation of ozone (O 3 ) to hydroxyl radicals (OH) by electro-generated H 2 O 2 , the E-peroxone process considerably enhanced dissolved organic carbon (DOC) abatement and significantly reduced bromate (BrO 3 - ) formation compared to conventional ozonation. However, natural organic matter (NOM) with high UV 254 absorbance, which is the major precursors of chlorination DBPs, was less efficiently abated during the E-peroxone process than conventional ozonation. Consequently, while both conventional ozonation and the E-peroxone process substantially reduced the formation of DBPs (trihalomethanes and haloacetic acids) during post-chlorination, higher DBP concentrations were generally observed during chlorination of the E-peroxone pretreated waters than conventional ozonation treated. In addition, because of conventional ozonation or the E-peroxone treatment, DBPs formed during post-chlorination shifted to more brominated species. The overall yields of brominated DBPs exhibited strong correlations with the bromide concentrations in water. Therefore, while the E-peroxone process can effectively suppress bromide transformation to bromate, it may lead to higher formation of brominated DBPs during post-chlorination compared to conventional ozonation. These results suggest that the E-peroxone process can lead to different DBP formation and speciation during water treatment trains compared to conventional ozonation. Copyright © 2017 Elsevier Ltd. All rights reserved.

Observations of HO{sub x}, NO{sub x}, NO{sub y}, and CO. NO{sub x} control of the photochemical production and removal of ozone in the upper troposphere

Energy Technology Data Exchange (ETDEWEB)

Wennberg, P O; Hanisco, T F; Lanzendorf, E L; Jaegle, L Y; Jacob, D J; Cohen, R C; Anderson, J G [Harvard Univ., Cambridge, MA (United States). Dept. of Chemistry; [Dept. of Earth and Planetary Sciences; Fahey, D W; Gao, R S; Keim, E R [National Oceanic and Atmospheric Administration, Boulder, CO (United States). Aeronomy Lab.; others, and

1998-12-31

In-situ measurements from the NASA ER2 aircraft provide the first observations of the odd-hydrogen radicals in the upper troposphere. A new photochemical model was constructed to explain the observations. Based on the model, the way of NO{sub x} influence on the photochemistry of ozone was determined. The measurements also explain why high NO{sub x}/NO{sub y} ratios are sustained in the upper troposphere. (R.P.)

Observations of HO{sub x}, NO{sub x}, NO{sub y}, and CO. NO{sub x} control of the photochemical production and removal of ozone in the upper troposphere

Energy Technology Data Exchange (ETDEWEB)

Wennberg, P.O.; Hanisco, T.F.; Lanzendorf, E.L.; Jaegle, L.Y.; Jacob, D.J.; Cohen, R.C.; Anderson, J.G. [Harvard Univ., Cambridge, MA (United States). Dept. of Chemistry]|[Dept. of Earth and Planetary Sciences; Fahey, D.W.; Gao, R.S.; Keim, E.R. [National Oceanic and Atmospheric Administration, Boulder, CO (United States). Aeronomy Lab.; and others

1997-12-31

In-situ measurements from the NASA ER2 aircraft provide the first observations of the odd-hydrogen radicals in the upper troposphere. A new photochemical model was constructed to explain the observations. Based on the model, the way of NO{sub x} influence on the photochemistry of ozone was determined. The measurements also explain why high NO{sub x}/NO{sub y} ratios are sustained in the upper troposphere. (R.P.)

Ozone phytotoxicity evaluation and prediction of crops production in tropical regions

Science.gov (United States)

Mohammed, Nurul Izma; Ramli, Nor Azam; Yahya, Ahmad Shukri

2013-04-01

Increasing ozone concentration in the atmosphere can threaten food security due to its effects on crop production. Since the 1980s, ozone has been believed to be the most damaging air pollutant to crops. In Malaysia, there is no index to indicate the reduction of crops due to the exposure of ozone. Therefore, this study aimed to identify the accumulated exposure over a threshold of X ppb (AOTX) indexes in assessing crop reduction in Malaysia. In European countries, crop response to ozone exposure is mostly expressed as AOT40. This study was designed to evaluate and predict crop reduction in tropical regions and in particular, the Malaysian climate, by adopting the AOT40 index method and modifying it based on Malaysian air quality and crop data. Nine AOTX indexes (AOT0, AOT5, AOT10, AOT15, AOT20, AOT25, AOT30, AOT40, and AOT50) were analyzed, crop responses tested and reduction in crops predicted. The results showed that the AOT50 resulted in the highest reduction in crops and the highest R2 value between the AOT50 and the crops reduction from the linear regression analysis. Hence, this study suggests that the AOT50 index is the most suitable index to estimate the potential ozone impact on crops in tropical regions. The result showed that the critical level for AOT50 index if the estimated crop reduction is 5% was 1336 ppb h. Additionally, the results indicated that the AOT40 index in Malaysia gave a minimum percentage of 6% crop reduction; as contrasted with the European guideline of 5% (due to differences in the climate e.g., average amount of sunshine).

Influence of synoptic condition and holiday effects on VOCs and ozone production in the Yangtze River Delta region, China

Science.gov (United States)

Xu, Zhengning; Huang, Xin; Nie, Wei; Chi, Xuguang; Xu, Zheng; Zheng, Longfei; Sun, Peng; Ding, Aijun

2017-11-01

Both anthropogenic emission and synoptic conditions play important roles in ozone (O3) formation and accumulation. In order to understand the influence of synoptic condition and holiday effects on ozone production in the Yangtze River Delta region, China, concentrations of speciated volatile organic compounds (VOCs) and O3 as well as other relevant trace gases were simultaneously measured at the Station for Observing Regional Processes of the Earth System (SORPES) in Nanjing around the National Day holidays of China in 2014, which featured substantial change of emissions and dominated by typical anti-cyclones. Different groups of VOC species and their chemical reactivities were comprehensively analyzed. We observed clear diurnal variations of short alkenes during the measurement period, considerable amount of short alkenes were observed during night (more than 10 ppb) while almost no alkenes were measured during daytime, which might be attributed to different chemical processes. The obvious enhancement of the VOC tracers during the National Day holidays (Oct. 1st-Oct. 7th) indicated that the holiday effect strongly influenced the distribution of VOC profile and chemical reactivity in the atmosphere. At the same time, two meso-scale anticyclone processes were also observed during the measurement period. The synoptic condition contributed to the accumulation of VOCs and other precursors, which consequently impacted the ozone production in this region. The integrated influence of synoptic and holiday effects was also analyzed with an Observation Based Model (OBM) based on simplified MCM (Master Chemical Mechanism) chemical mechanism. The calculated relative increment reactivity (RIR) of different VOC groups revealed that during the holidays, this region was in VOC-limited regime and the variation of RIR shows a close linkage to the development and elimination of anti-cyclones, indicating an in-negligible contribution of synoptic effect toward ozone production in this

Understanding in situ ozone production in the summertime through radical observations and modelling studies during the Clean air for London project (ClearfLo)

Science.gov (United States)

Whalley, Lisa K.; Stone, Daniel; Dunmore, Rachel; Hamilton, Jacqueline; Hopkins, James R.; Lee, James D.; Lewis, Alastair C.; Williams, Paul; Kleffmann, Jörg; Laufs, Sebastian; Woodward-Massey, Robert; Heard, Dwayne E.

2018-02-01

Measurements of OH, HO2, RO2i (alkene and aromatic-related RO2) and total RO2 radicals taken during the ClearfLo campaign in central London in the summer of 2012 are presented. A photostationary steady-state calculation of OH which considered measured OH reactivity as the OH sink term and the measured OH sources (of which HO2+ NO reaction and HONO photolysis dominated) compared well with the observed levels of OH. Comparison with calculations from a detailed box model utilising the Master Chemical Mechanism v3.2, however, highlighted a substantial discrepancy between radical observations under lower NOx conditions ([NO] model was missing a significant peroxy radical sink; the model overpredicted HO2 by up to a factor of 10 at these times. Known radical termination steps, such as HO2 uptake on aerosols, were not sufficient to reconcile the model-measurement discrepancies alone, suggesting other missing termination processes. This missing sink was most evident when the air reaching the site had previously passed over central London to the east and when elevated temperatures were experienced and, hence, contained higher concentrations of VOCs. Uncertainties in the degradation mechanism at low NOx of complex biogenic and diesel related VOC species, which were particularly elevated and dominated OH reactivity under these easterly flows, may account for some of the model-measurement disagreement. Under higher [NO] (> 3 ppbv) the box model increasingly underpredicted total [RO2]. The modelled and observed HO2 were in agreement, however, under elevated NO concentrations ranging from 7 to 15 ppbv. The model uncertainty under low NO conditions leads to more ozone production predicted using modelled peroxy radical concentrations ( ˜ 3 ppbv h-1) versus ozone production from peroxy radicals measured ( ˜ 1 ppbv h-1). Conversely, ozone production derived from the predicted peroxy radicals is up to an order of magnitude lower than from the observed peroxy radicals as [NO

Observations of ozone formation in power plant plumes and implications for ozone control strategies

Energy Technology Data Exchange (ETDEWEB)

Ryerson, T.B.; Trainer, M.; Holloway, J.S.; Parrish, D.D.; Huey, L.G.; Sueper, D.T.; Frost, G.J.; Donnelly, S.G.; Schauffler, S.; Atlas, E.L.; Kuster, W.C.; Goldan, P.D.; Huebler, G.; Meagher, J.F.; Fehsenfeld, F.C. [NOAA, Boulder, CO (USA). Aeronomy Lab.

2001-04-27

Data taken in aircraft transects of emissions plumes from rural US coal-fired power plants were used to confirm and quantify the nonlinear dependence of tropospheric ozone formation on plume NOx (NO plus NO{sub 2}) concentration, which is determined by plant NOx emission rate and atmospheric dispersion. The ambient availability of reactive volatile organic compounds, principally biogenic isoprene, was also found to modular ozone production rate and yield in these rural plumes. Differences of a factor of 2 or greater in plume ozone formation rates and yields as a function of NOx and volatile organic compound concentrations were consistently observed. These large differences suggest that consideration of power plant NOx emission rates and geographic locations in current and future US ozone control strategies could substantially enhance the efficacy of NOx reductions from these sources. 18 refs., 4 figs.

Tropospheric Ozone Pollution from Space: New Views from the TOMS (Total Ozone Mapping Spectrometer) Instrument

Science.gov (United States)

Thompson, Anne M.; Hudson, Robert D.; Frolov, Alexander D.; Witte, Jacquelyn C.; Kucsera, Tom L.; Einaudi, Franco (Technical Monitor)

2000-01-01

New products from the TOMS (Total Ozone Mapping Spectrometer) >satellite instrument can resolve pollution events in tropical and mid-latitudes, Over the past several years, we have developed tropospheric ozone data sets by two methods. The modified-residual technique [Hudson and Thompson, 1998; Thompson and Hudson, 1999] uses v. 7 TOMS total ozone and is applicable to tropical regimes in which the wave-one pattern in total ozone is observed. The TOMSdirect method [Hudson et at., 2000] represents a new algorithm that uses TOMS radiances to extract tropospheric ozone in regions of constant stratospheric ozone and tropospheric ozone displaying high mixing ratios and variability characteristic of pollution, Absorbing aerosols (dust and smoke; Herman et at., 1997 Hsu et al., 1999), a standard TOMS product, provide transport and/or source marker information to interpret tropospheric ozone. For the Nimbus 7/TOMS observing period (1979-1992), modified-residual TTO (tropical tropospheric ozone) appears as two maps/month at I-degree latitude 2-degree longitude resolution at a homepage and digital data are available (20S to 20N) by ftp at http://metosrv2. umd.edu/tropo/ 14y_data.d. Preliminary modified-residual TTO data from the operational Earth-Probe/TOMS (1996- present) are posted in near-real-time at the same website. Analyses with the new tropospheric ozone and aerosol data are illustrated by the following (I)Signals in tropical tropospheric ozone column and smoke amount during ENSO (El Nino-Southern Oscillation) events, e.g. 1982-1983 and the intense ENSO induced biomass fires of 1997-1998 over the Indonesian region [Thompson et a[, 2000a, Thompson and Hudson, 1999]. (2) Trends in tropospheric ozone and smoke aerosols in various tropical regions (Atlantic, Pacific, Africa, Brazil). No significant trends were found for ozone from1980-1990 [Thompson and Hudson, 19991 although smoke aerosols increased during the period [Hsu et al.,1999]. (3) Temporal and spatial offsets

OMI/Aura Ozone (O3) Total Column 1-Orbit L2 Swath 13x24 km V003 NRT

Data.gov (United States)

National Aeronautics and Space Administration — The OMI/Aura Level-2 Total Column Ozone Data Product OMTO3 Near Real Time data is made available from the OMI SIPS NASA for the public access. The Ozone Monitoring...

Evaluation of the persistence of transformation products from ozonation of trace organic compounds - a critical review.

Science.gov (United States)

Hübner, Uwe; von Gunten, Urs; Jekel, Martin

2015-01-01

Ozonation is an efficient treatment system to reduce the concentration of trace organic compounds (TrOCs) from technical aquatic systems such as drinking water, wastewater and industrial water, etc. Although it is well established that ozonation generally improves the removal of organic matter in biological post-treatment, little is known about the biodegradability of individual transformation products resulting from ozonation of TrOCs. This publication provides a qualified assessment of the persistence of ozone-induced transformation products based on a review of published product studies and an evaluation of the biodegradability of transformation products with the biodegradability probability program (BIOWIN) and the University of Minnesota Pathway Prediction System (UM-PPS). The oxidation of TrOCs containing the four major ozone-reactive sites (olefins, amines, aromatics and sulfur-containing compounds) follows well described reaction pathways leading to characteristic transformation products. Assessment of biodegradability revealed a high sensitivity to the formed products and hence the ozone-reactive site present in the target compound. Based on BIOWIN, efficient removal can be expected for products from cleavage of olefin groups and aromatic rings. In contrast, estimations and literature indicate that hydroxylamines and N-oxides, the major products from ozonation of secondary and tertiary amines are not necessarily better removed in biological post-treatment. According to UM-PPS, degradation of these products might even occur via reformation of the corresponding amine. Some product studies with sulfide-containing TrOCs showed a stoichiometric formation of sulfoxides from oxygen transfer reactions. However, conclusions on the fate of transformation products in biological post-treatment cannot be drawn based on BIOWIN and UM-PPS.

MERRA 3D IAU Tendency, Ozone, Time average 3-hourly (1.25x1.25L42) V5.2.0

Data.gov (United States)

National Aeronautics and Space Administration — The MAT3CPODT or tavg3_3d_odt_Cp data product is the MERRA Data Assimilation System 3-Dimensional ozone tendencies that is time averaged on pressure levels at a...

Sources of HO x and production of ozone in the upper troposphere over the United States

OpenAIRE

Jaeglé, L.; Jacob, Daniel James; Brune, W. H.; Tan, D.; Faloona, I. C.; Weinheimer, A. J.; Ridley, B. A.; Campos, T. L.; Sachse, G. W.

1998-01-01

The sources of HOx (OH+peroxy radicals) and the associated production of ozone at 8–12 km over the United States are examined by modeling observations of OH, HO2, NO, and other species during the SUCCESS aircraft campaign in April–May 1996. The HOx concentrations measured in SUCCESS are up to a factor of 3 higher than can be calculated from oxidation of water vapor and photolysis of acetone. The highest discrepancy was seen in the outflow of a convective storm. We show that convective injecti...

Variability of indicator values for ozone production sensitivity: a model study in Switzerland and San Joaquin Valley (California)

International Nuclear Information System (INIS)

Andreani-Aksoyoglu, S.; Keller, J.; Prevot, A.S.H.; Chenghsuan Lu; Chang, J.S.

2001-01-01

The threshold values of indicator species and ratios delineating the transition between NO x and VOC sensitivity of ozone formation are assumed to be universal by various investigators. However, our previous studies suggested that threshold values might vary according to the locations and conditions. In this study, threshold values derived from various model simulations at two different locations (the area of Switzerland by UAM Model and San Joaquin Valley of Central California by SAQM Model) are examined using a new approach for defining NO x and VOC sensitive regimes. Possible definitions for the distinction of NO x and VOC sensitive ozone production regimes are given. The dependence of the threshold values for indicators and indicator ratios such as NO y , O 3 /NO z , HCHO/NO y , and H 2 O 2 /HNO 3 on the definition of NO x and VOC sensitivity is discussed. Then the variations of threshold values under low emission conditions and in two different days are examined in both areas to check whether the models respond consistently to changes in environmental conditions. In both cases, threshold values are shifted similarly when emissions are reduced. Changes in the wind fields and aging of the photochemical oxidants seem to cause the day-to-day variation of the threshold values. O 3 /NO z and HCHO/NO y indicators are predicted to be unsatisfactory to separate the NO x and VOC sensitive regimes. Although NO y and H 2 O 2 /HNO 3 provide a good separation of the two regimes, threshold values are affected by changes in the environmental conditions studied in this work. (author)

Low modeled ozone production suggests underestimation of precursor emissions (especially NOx in Europe

Directory of Open Access Journals (Sweden)

E. Oikonomakis

2018-02-01

Full Text Available High surface ozone concentrations, which usually occur when photochemical ozone production takes place, pose a great risk to human health and vegetation. Air quality models are often used by policy makers as tools for the development of ozone mitigation strategies. However, the modeled ozone production is often not or not enough evaluated in many ozone modeling studies. The focus of this work is to evaluate the modeled ozone production in Europe indirectly, with the use of the ozone–temperature correlation for the summer of 2010 and to analyze its sensitivity to precursor emissions and meteorology by using the regional air quality model, the Comprehensive Air Quality Model with Extensions (CAMx. The results show that the model significantly underestimates the observed high afternoon surface ozone mixing ratios (≥  60 ppb by 10–20 ppb and overestimates the lower ones (<  40 ppb by 5–15 ppb, resulting in a misleading good agreement with the observations for average ozone. The model also underestimates the ozone–temperature regression slope by about a factor of 2 for most of the measurement stations. To investigate the impact of emissions, four scenarios were tested: (i increased volatile organic compound (VOC emissions by a factor of 1.5 and 2 for the anthropogenic and biogenic VOC emissions, respectively, (ii increased nitrogen oxide (NOx emissions by a factor of 2, (iii a combination of the first two scenarios and (iv increased traffic-only NOx emissions by a factor of 4. For southern, eastern, and central (except the Benelux area Europe, doubling NOx emissions seems to be the most efficient scenario to reduce the underestimation of the observed high ozone mixing ratios without significant degradation of the model performance for the lower ozone mixing ratios. The model performance for ozone–temperature correlation is also better when NOx emissions are doubled. In the Benelux area, however, the third scenario

Regulation of ozone-induced lung inflammation and injury by the β-galactoside-binding lectin galectin-3

Energy Technology Data Exchange (ETDEWEB)

Sunil, Vasanthi R., E-mail: sunilva@pharmacy.rutgers.edu [Department of Pharmacology and Toxicology, Rutgers University, Ernest Mario School of Pharmacy, Piscataway, NJ (United States); Francis, Mary, E-mail: maryfranrutgers@gmail.com [Department of Pharmacology and Toxicology, Rutgers University, Ernest Mario School of Pharmacy, Piscataway, NJ (United States); Vayas, Kinal N., E-mail: kinalv5@gmail.com [Department of Pharmacology and Toxicology, Rutgers University, Ernest Mario School of Pharmacy, Piscataway, NJ (United States); Cervelli, Jessica A., E-mail: j.cervelli@pharmacy.rutgers.edu [Department of Pharmacology and Toxicology, Rutgers University, Ernest Mario School of Pharmacy, Piscataway, NJ (United States); Choi, Hyejeong, E-mail: choi@eohsi.rutgers.edu [Department of Pharmacology and Toxicology, Rutgers University, Ernest Mario School of Pharmacy, Piscataway, NJ (United States); Laskin, Jeffrey D., E-mail: jlaskin@eohsi.rutgers.edu [Department of Environmental and Occupational Medicine, Rutgers University, Robert Wood Johnson Medical School, Piscataway, NJ (United States); Laskin, Debra L., E-mail: laskin@eohsi.rutgers.edu [Department of Pharmacology and Toxicology, Rutgers University, Ernest Mario School of Pharmacy, Piscataway, NJ (United States)

2015-04-15

Macrophages play a dual role in ozone toxicity, contributing to both pro- and anti-inflammatory processes. Galectin-3 (Gal-3) is a lectin known to regulate macrophage activity. Herein, we analyzed the role of Gal-3 in the response of lung macrophages to ozone. Bronchoalveolar lavage (BAL) and lung tissue were collected 24–72 h after exposure (3 h) of WT and Gal-3{sup -/-} mice to air or 0.8 ppm ozone. In WT mice, ozone inhalation resulted in increased numbers of proinflammatory (Gal-3{sup +}, iNOS{sup +}) and anti-inflammatory (MR-1{sup +}) macrophages in the lungs. While accumulation of iNOS{sup +} macrophages was attenuated in Gal-3{sup -/-} mice, increased numbers of enlarged MR-1{sup +} macrophages were noted. This correlated with increased numbers of macrophages in BAL. Flow cytometric analysis showed that these cells were CD11b{sup +} and consisted mainly (> 97%) of mature (F4/80{sup +}CD11c{sup +}) proinflammatory (Ly6GLy6C{sup hi}) and anti-inflammatory (Ly6GLy6C{sup lo}) macrophages. Increases in both macrophage subpopulations were observed following ozone inhalation. Loss of Gal-3 resulted in a decrease in Ly6C{sup hi} macrophages, with no effect on Ly6C{sup lo} macrophages. CD11b{sup +}Ly6G{sup +}Ly6C{sup +} granulocytic (G) and monocytic (M) myeloid derived suppressor cells (MDSC) were also identified in the lung after ozone. In Gal-3{sup -/-} mice, the response of G-MDSC to ozone was attenuated, while the response of M-MDSC was heightened. Changes in inflammatory cell populations in the lung of ozone treated Gal-3{sup -/-} mice were correlated with reduced tissue injury as measured by cytochrome b5 expression. These data demonstrate that Gal-3 plays a role in promoting proinflammatory macrophage accumulation and toxicity in the lung following ozone exposure. - Highlights: • Multiple monocytic-macrophage subpopulations accumulate in the lung after ozone inhalation. • Galectin-3 plays a proinflammatory role in ozone-induced lung injury. • In the

Numerical modelling of ozone production in a wire-cylinder corona discharge and comparison with a wire-plate corona discharge

International Nuclear Information System (INIS)

Wang Pengxiang; Chen Junhong

2009-01-01

The effect of electrode configuration on ozone production in the direct-current corona discharge of dry and humid air is studied by a numerical model that combines the electron distribution in the corona plasma, plasma chemistry and transport phenomena. Two electrode configurations are considered: wire-cylinder discharge with air flowing along the wire axis and wire-plate discharge with air flowing transverse to the wire. The ozone distributions in both types of discharges are compared. For both electrode configurations, the ozone production rate is higher in the negative corona than in the positive corona and it decreases with an increase in relative humidity. More importantly, the detailed ozone distribution in the neighbourhood of the discharge wire, together with the ozone kinetics, reveals the possible difference in the ozone production from the two discharges. With the same operating conditions and sufficiently short flow residence time, the ozone production rate is nearly the same for both electrode configurations. When the flow residence time is longer than the characteristic time for homogeneous ozone destruction, the net ozone production is higher in the wire-cylinder discharge than in the wire-plate discharge due to relatively less ozone destruction.

Numerical modelling of ozone production in a wire-cylinder corona discharge and comparison with a wire-plate corona discharge

Science.gov (United States)

Wang, Pengxiang; Chen, Junhong

2009-02-01

The effect of electrode configuration on ozone production in the direct-current corona discharge of dry and humid air is studied by a numerical model that combines the electron distribution in the corona plasma, plasma chemistry and transport phenomena. Two electrode configurations are considered: wire-cylinder discharge with air flowing along the wire axis and wire-plate discharge with air flowing transverse to the wire. The ozone distributions in both types of discharges are compared. For both electrode configurations, the ozone production rate is higher in the negative corona than in the positive corona and it decreases with an increase in relative humidity. More importantly, the detailed ozone distribution in the neighbourhood of the discharge wire, together with the ozone kinetics, reveals the possible difference in the ozone production from the two discharges. With the same operating conditions and sufficiently short flow residence time, the ozone production rate is nearly the same for both electrode configurations. When the flow residence time is longer than the characteristic time for homogeneous ozone destruction, the net ozone production is higher in the wire-cylinder discharge than in the wire-plate discharge due to relatively less ozone destruction.

Ozonated Olive Oils and Troubles

Directory of Open Access Journals (Sweden)

Bulent Uysal

2014-04-01

Full Text Available One of the commonly used methods for ozone therapy is ozonated oils. Most prominent type of used oils is extra virgin olive oil. But still, each type of unsaturated oils may be used for ozonation. There are a lot of wrong knowledge on the internet about ozonated oils and its use as well. Just like other ozone therapy studies, also the studies about ozone oils are inadequate to avoid incorrect knowledge. Current data about ozone oil and its benefits are produced by supplier who oversees financial interests and make misinformation. Despite the rapidly increasing ozone oil sales through the internet, its quality and efficacy is still controversial. Dozens of companies and web sites may be easily found to buy ozonated oil. But, very few of these products are reliable, and contain sufficiently ozonated oil. This article aimed to introduce the troubles about ozonated oils and so to inform ozonated oil users. [J Intercult Ethnopharmacol 2014; 3(2.000: 49-50

Ozone response to emission changes: a modeling study during the MCMA-2006/MILAGRO Campaign

Directory of Open Access Journals (Sweden)

J. Song

2010-04-01

Full Text Available The sensitivity of ozone production to precursor emissions was investigated under five different meteorological conditions in the Mexico City Metropolitan Area (MCMA during the MCMA-2006/MILAGRO field campaign using the gridded photochemical model CAMx driven by observation-nudged WRF meteorology. Precursor emissions were constrained by the comprehensive data from the field campaign and the routine ambient air quality monitoring network. Simulated plume mixing and transport were examined by comparing with measurements from the G-1 aircraft during the campaign. The observed concentrations of ozone precursors and ozone were reasonably well reproduced by the model. The effects of reducing precursor emissions on urban ozone production were performed for three representative emission control scenarios. A 50% reduction in VOC emissions led to 7 to 22 ppb decrease in daily maximum ozone concentrations, while a 50% reduction in NO_x emissions leads to 4 to 21 ppb increase, and 50% reductions in both NO_x and VOC emission decrease the daily maximum ozone concentrations up to 10 ppb. These results along with a chemical indicator analysis using the chemical production ratios of H₂O₂ to HNO₃ demonstrate that the MCMA urban core region is VOC-limited for all meteorological episodes, which is consistent with the results from MCMA-2003 field campaign; however the degree of the VOC-sensitivity is higher during MCMA-2006 due to lower VOCs, lower VOC reactivity and moderately higher NO_x emissions. Ozone formation in the surrounding mountain/rural area is mostly NO_x-limited, but can be VOC-limited, and the range of the NO_x-limited or VOC-limited areas depends on meteorology.

Aromatic VOCs global influence in the ozone production

Science.gov (United States)

Cabrera-Perez, David; Pozzer, Andrea

2016-04-01

Aromatic hydrocarbons are a subgroup of Volatile Organic Compounds (VOCs) of special interest in the atmosphere of urban and semi-urban areas. Aromatics form a high fraction of VOCs, are highly reactive and upon oxidation they are an important source of ozone. These group of VOCs are released to the atmosphere by processes related to biomass burning and fossil fuel consumption, while they are removed from the atmosphere primarily by OH reaction and by dry deposition. In addition, a branch of aromatics (ortho-nitrophenols) produce HONO upon photolysis, which is responsible of certain amount of the OH recycling. Despite their importance in the atmosphere in anthropogenic polluted areas, the influence of aromatics in the ozone production remains largely unknown. This is of particular relevance, being ozone a pollutant with severe side effects on air quality, health and climate. In this work the atmospheric impacts at global scale of the most emitted aromatic VOCs in the gas phase (benzene, toluene, xylenes, ethylbenzene, styrene, phenol, benzaldehyde and trimethylbenzenes) are analysed and assessed. Specifically, the impact on ozone due to aromatic oxidation is estimated, as this is of great interest in large urban areas and can be helpful for developing air pollution control strategies. Further targets are the quantification of the NOx loss and the OH recycling due to aromatic oxidation. In order to investigate these processes, two simulations were performed with the numerical chemistry and climate simulation ECHAM/MESSy Atmospheric Chemistry (EMAC) model. The simulations compare two cases, one with ozone concentrations when aromatics are present or the second one when they are missing. Finally, model simulated ozone is compared against a global set of observations in order to better constrain the model accuracy.

TOMS/Nimbus-7 Total Column Ozone Monthly L3 Global 1x1.25 deg Lat/Lon Grid V008

Data.gov (United States)

National Aeronautics and Space Administration — This data product contains TOMS/Nimbus-7 Total Column Ozone Monthly L3 Global 1x1.25 deg Lat/Lon Grid Version 8 data in ASCII format. The Total Ozone Mapping...

TOMS/Nimbus-7 Total Column Ozone Daily L3 Global 1x1.25 deg Lat/Lon Grid V008

Data.gov (United States)

National Aeronautics and Space Administration — This data product contains TOMS/Nimbus-7 Total Column Ozone Daily L3 Global 1x1.25 deg Lat/Lon Grid Version 8 data in ASCII format. The Total Ozone Mapping...

Rapid Removal of Tetrabromobisphenol A by Ozonation in Water: Oxidation Products, Reaction Pathways and Toxicity Assessment.

Directory of Open Access Journals (Sweden)

Ruijuan Qu

Full Text Available Tetrabromobisphenol A (TBBPA is one of the most widely used brominated flame retardants and has attracted more and more attention. In this work, the parent TBBPA with an initial concentration of 100 mg/L was completely removed after 6 min of ozonation at pH 8.0, and alkaline conditions favored a more rapid removal than acidic and neutral conditions. The presence of typical anions and humic acid did not significantly affect the degradation of TBBPA. The quenching test using isopropanol indicated that direct ozone oxidation played a dominant role during this process. Seventeen reaction intermediates and products were identified using an electrospray time-of-flight mass spectrometer. Notably, the generation of 2,4,6-tribromophenol was first observed in the degradation process of TBBPA. The evolution of reaction products showed that ozonation is an efficient treatment for removal of both TBBPA and intermediates. Sequential transformation of organic bromine to bromide and bromate was confirmed by ion chromatography analysis. Two primary reaction pathways that involve cleavage of central carbon atom and benzene ring cleavage concomitant with debromination were thus proposed and further justified by calculations of frontier electron densities. Furthermore, the total organic carbon data suggested a low mineralization rate, even after the complete removal of TBBPA. Meanwhile, the acute aqueous toxicity of reaction solutions to Photobacterium Phosphoreum and Daphnia magna was rapidly decreased during ozonation. In addition, no obvious difference in the attenuation of TBBPA was found by ozone oxidation using different water matrices, and the effectiveness in natural waters further demonstrates that ozonation can be adopted as a promising technique to treat TBBPA-contaminated waters.

Rapid Removal of Tetrabromobisphenol A by Ozonation in Water: Oxidation Products, Reaction Pathways and Toxicity Assessment

Science.gov (United States)

Wang, Xinghao; Huang, Qingguo; Lu, Junhe; Wang, Liansheng; Wang, Zunyao

2015-01-01

Tetrabromobisphenol A (TBBPA) is one of the most widely used brominated flame retardants and has attracted more and more attention. In this work, the parent TBBPA with an initial concentration of 100 mg/L was completely removed after 6 min of ozonation at pH 8.0, and alkaline conditions favored a more rapid removal than acidic and neutral conditions. The presence of typical anions and humic acid did not significantly affect the degradation of TBBPA. The quenching test using isopropanol indicated that direct ozone oxidation played a dominant role during this process. Seventeen reaction intermediates and products were identified using an electrospray time-of-flight mass spectrometer. Notably, the generation of 2,4,6-tribromophenol was first observed in the degradation process of TBBPA. The evolution of reaction products showed that ozonation is an efficient treatment for removal of both TBBPA and intermediates. Sequential transformation of organic bromine to bromide and bromate was confirmed by ion chromatography analysis. Two primary reaction pathways that involve cleavage of central carbon atom and benzene ring cleavage concomitant with debromination were thus proposed and further justified by calculations of frontier electron densities. Furthermore, the total organic carbon data suggested a low mineralization rate, even after the complete removal of TBBPA. Meanwhile, the acute aqueous toxicity of reaction solutions to Photobacterium Phosphoreum and Daphnia magna was rapidly decreased during ozonation. In addition, no obvious difference in the attenuation of TBBPA was found by ozone oxidation using different water matrices, and the effectiveness in natural waters further demonstrates that ozonation can be adopted as a promising technique to treat TBBPA-contaminated waters. PMID:26430733

Operational surface UV radiation product from GOME-2 and AVHRR/3 data

OpenAIRE

J. Kujanpää; N. Kalakoski

2015-01-01

The surface ultraviolet (UV) radiation product, version 1.20, generated operationally in the framework of the Satellite Application Facility on Ozone and Atmospheric Chemistry Monitoring (O3M SAF) of the European Organisation for the Exploitation of Meteorological Satellites (EUMETSAT) is described. The product is based on the total ozone column derived from the measurements of the second Global Ozone Monitoring Experiment (GOME-2) instrument aboard EUMETSA...

Catalytic ozonation of ammonia using biomass char and wood fly ash.

Science.gov (United States)

Kastner, James R; Miller, Joby; Kolar, Praveen; Das, K C

2009-05-01

Catalytic ozonation of gaseous ammonia was investigated at room temperature using wood fly ash (WFA) and biomass char as catalysts. WFA gave the best results, removing ammonia (11 ppmv NH(3), 45% conversion) at 23 degrees C at a residence time of 0.34 s, using 5 g of catalyst or ash at the lowest ozone concentration (62 ppmv). Assuming pseudo zero order kinetics in ozone, a power rate law of -r(NH3) = 7.2 x 10(-8) C(NH3)(0.25) (r, mol g(-1)s(-1), C(NH3)molL(-1)) was determined at 510 ppmv O(3) and 23 degrees C for WFA. Water vapor approximately doubled the oxidation rate using WFA and catalytic ozonation activity was not measured for the char without humidifying the air stream. Overall oxidation rates using the crude catalysts were lower than commercial catalysts, but the catalytic ozonation process operated at significantly lower temperatures (23 vs. 300 degrees C). Nitric oxide was not detected and the percentage of NO(2) formed from NH(3) oxidation ranged from 0.3% to 3% (v/v), with WFA resulting in the lowest NO(2) level (at low O(3) levels). However, we could not verify that N(2)O was not formed, so further research is needed to determine if N(2) is the primary end-product. Additional research is required to develop techniques to enhance the oxidation activity and industrial application of the crude, but potentially inexpensive catalysts.

Ozone pretreatment of process waste water generated in course of fluoroquinolone production.

Science.gov (United States)

Daoud, Fares; Pelzer, David; Zuehlke, Sebastian; Spiteller, Michael; Kayser, Oliver

2017-10-01

During production of active pharmaceutical ingredients, process waste water is generated at several stages of manufacturing. Whenever possible, the resulting waste water will be processed by conventional waste water treatment plants. Currently, incineration of the process waste water is the method to eliminate compounds with high biological activity. Thus, ozone treatment followed by biological waste water treatment was tested as an alternative method. Two prominent representatives of the large group of fluoroquinolone antibiotics (ciprofloxacin and moxifloxacin) were investigated, focussing on waste water of the bulk production. Elimination of the target compounds and generation of their main transformation products were determined by liquid chromatography - high resolution mass spectrometry (LC-HRMS). The obtained results demonstrated, that the concentration of moxifloxacin and its metabolites can be effectively reduced (>99.7%) prior entering the receiving water. On the contrary, the concentration of ciprofloxacin and its metabolites remained too high for safe discharge, necessitating application of prolonged ozonation for its further degradation. The required ozonation time can be estimated based on the determined kinetics. To assure a low biological activity the ecotoxicity of the ozonated waste water was investigated using three trophic levels. By means of multiple-stage mass spectrometry (MS n ) experiments several new transformation products of the fluoroquinolones were identified. Thus, previously published proposed structures could be corrected or confirmed. Copyright © 2017 Elsevier Ltd. All rights reserved.

Ozone kinetics in low-pressure discharges: vibrationally excited ozone and molecule formation on surfaces

Science.gov (United States)

Marinov, Daniil; Guerra, Vasco; Guaitella, Olivier; Booth, Jean-Paul; Rousseau, Antoine

2013-10-01

A combined experimental and modeling investigation of the ozone kinetics in the afterglow of pulsed direct current discharges in oxygen is carried out. The discharge is generated in a cylindrical silica tube of radius 1 cm, with short pulse durations between 0.5 and 2 ms, pressures in the range 1-5 Torr and discharge currents ˜40-120 mA. Time-resolved absolute concentrations of ground-state atoms and ozone molecules were measured simultaneously in situ, by two-photon absorption laser-induced fluorescence and ultraviolet absorption, respectively. The experiments were complemented by a self-consistent model developed to interpret the results and, in particular, to evaluate the roles of vibrationally excited ozone and of ozone formation on surfaces. It is found that vibrationally excited ozone, O_3^{*} , plays an important role in the ozone kinetics, leading to a decrease in the ozone concentration and an increase in its formation time. In turn, the kinetics of O_3^{*} is strongly coupled with those of atomic oxygen and O2(a 1Δg) metastables. Ozone formation at the wall does not contribute significantly to the total ozone production under the present conditions. Upper limits for the effective heterogeneous recombination probability of O atoms into ozone are established.

Ozone kinetics in low-pressure discharges: vibrationally excited ozone and molecule formation on surfaces

International Nuclear Information System (INIS)

Marinov, Daniil; Guaitella, Olivier; Booth, Jean-Paul; Rousseau, Antoine; Guerra, Vasco

2013-01-01

A combined experimental and modeling investigation of the ozone kinetics in the afterglow of pulsed direct current discharges in oxygen is carried out. The discharge is generated in a cylindrical silica tube of radius 1 cm, with short pulse durations between 0.5 and 2 ms, pressures in the range 1–5 Torr and discharge currents ∼40–120 mA. Time-resolved absolute concentrations of ground-state atoms and ozone molecules were measured simultaneously in situ, by two-photon absorption laser-induced fluorescence and ultraviolet absorption, respectively. The experiments were complemented by a self-consistent model developed to interpret the results and, in particular, to evaluate the roles of vibrationally excited ozone and of ozone formation on surfaces. It is found that vibrationally excited ozone, O 3 * , plays an important role in the ozone kinetics, leading to a decrease in the ozone concentration and an increase in its formation time. In turn, the kinetics of O 3 * is strongly coupled with those of atomic oxygen and O 2 (a 1 Δ g ) metastables. Ozone formation at the wall does not contribute significantly to the total ozone production under the present conditions. Upper limits for the effective heterogeneous recombination probability of O atoms into ozone are established. (paper)

Tropospheric Ozone as a Short-lived Chemical Climate Forcer

Science.gov (United States)

Pickering, Kenneth E.

2012-01-01

Tropospheric ozone is the third most important greenhouse gas according to the most recent IPCC assessment. However, tropospheric ozone is highly variable in both space and time. Ozone that is located in the vicinity of the tropopause has the greatest effect on climate forcing. Nitrogen oxides (NOx) are the most important precursors for ozone In most of the troposphere. Therefore, pollution that is lofted upward in thunderstorm updrafts or NOx produced by lightning leads to efficient ozone production in the upper troposphere, where ozone is most important climatically. Global and regional model estimates of the impact of North American pollution and lightning on ozone radiative forcing will be presented. It will be shown that in the Northern Hemisphere summer, the lightning effect on ozone radiative forcing can dominate over that of pollution, and that the radiative forcing signal from North America extends well into Europe and North Africa. An algorithm for predicting lightning flash rates and estimating lightning NOx emissions is being incorporated into the NASA GEOS-5 Chemistry and Climate Model. Changes in flash rates and emissions over an ENSO cycle and in future climates will be assessed, along with the resulting changes in upper tropospheric ozone. Other research on the production of NOx per lightning flash and its distribution in the vertical based on cloud-resolving modeling and satellite observations will be presented. Distributions of NO2 and O3 over the Middle East from the OMI instrument on NASA's Aura satellite will also be shown.

Peroxy radical chemistry and the control of ozone photochemistry at Mace Head, Ireland during the summer of 2002

Directory of Open Access Journals (Sweden)

Z. L. Fleming

2006-01-01

Full Text Available Peroxy radical (HO2+ΣRO2 measurements, using the PEroxy Radical Chemical Amplification (PERCA technique at the North Atlantic Marine Boundary Layer EXperiment (NAMBLEX at Mace Head in summer 2002, are presented and put into the context of marine, boundary-layer chemistry. A suite of other chemical parameters (NO, NO2, NO3, CO, CH4, O3, VOCs, peroxides, photolysis frequencies and meteorological measurements, are used to present a detailed analysis of the role of peroxy radicals in tropospheric oxidation cycles and ozone formation. Under the range of conditions encountered the peroxy radical daily maxima varied from 10 to 40 pptv. The diurnal cycles showed an asymmetric shape typically shifted to the afternoon. Using a box model based on the master chemical mechanism the average model measurement agreement was 2.5 across the campaign. The addition of halogen oxides to the model increases the level of model/measurement agreement, apparently by respeciation of HOx. A good correlation exists between j(HCHO.[HCHO] and the peroxy radicals indicative of the importance of HCHO in the remote atmosphere as a HOx source, particularly in the afternoon. The peroxy radicals showed a strong dependence on [NO2] with a break point at 0.1 ppbv, where the radicals increased concomitantly with the reactive VOC loading, this is a lower value than seen at representative urban campaigns. The HO2/(HO2+ΣRO2 ratios are dependent on [NOx] ranging between 0.2 and 0.6, with the ratio increasing linearly with NOx. Significant night-time levels of peroxy radicals were measured up to 25 pptv. The contribution of ozone-alkenes and NO3-alkene chemistry to night-time peroxy radical production was shown to be on average 59 and 41%. The campaign mean net ozone production rate was 0.11±0.3 ppbv h-1. The ozone production rate was strongly dependent on [NO] having linear sensitivity (dln(P(O3/dln(NO=1.0. The results imply that the N(O3 (the in-situ net photochemical rate of ozone

Hydrogen Radicals, Nitrogen Radicals, and the Production of O3 in the Upper Troposphere

Science.gov (United States)

Wennberg, P. O.; Hanisco, T. F.; Jaegle, L.; Jacob, D. J.; Hintsa, E. J.; Lanzendorf, E. J.; Anderson, J. G.; Gao, R.-S.; Keim, E. R.; Donnelly, S. G.;

Reclaimed water quality during simulated ozone-managed aquifer recharge hybrid

KAUST Repository

Yoon, Min

2014-06-17

A synergistic hybrid of two treatment processes, managed aquifer recharge (MAR) combined with ozonation, was proposed for wastewater reclamation and water reuse applications. Batch reactor and soil-column experiments were performed to evaluate reclaimed water quality using various chemical and bacterial analyses. The ozone process was optimized at low ozone dose (0.5 mg O3/mg DOC) based on the control of N-nitrosodimethylamine (<5 ng L-1) and bromate (<10 μg L-1), and applied prior to (i.e., O3-MAR) and after MAR (i.e., MAR-O3). This work demonstrates that effluent organic matter (EfOM) and trace organic contaminants (TOrCs) are effectively removed during the hybrid process of MAR combined ozonation, compared to MAR only. Based on fluorescence excitation-emission matrices analyses, both MAR and ozonation reduce soluble microbial (protein-like) products while only ozonation contributes in reducing humic and fulvic substances. Even at low ozone dose of 0.5 mg O3/mg DOC, the O3-MAR hybrid significantly reduced UV absorbance by ≥2 m-1, BDOC by ≥64 %, and total (Σ) TOrC concentrations by ≥70 % in the effluent water quality. However, no significant improvement (<10 %) in the removal of Σ16 TOrC concentrations was observed for the increased ozone dose at 1.0 mg O3/mg DOC during MAR combined ozonation processes. Overall, O3-MAR was effective by 10-30 % in treating effluent water than MAR based on DOC, UV254 nm EfOM, TOrC and bacterial analyses. In addition, MAR-O3 was better than O3-MAR for the reduction of fluorescence (close MQ), TOrCs (≥74 %) and total bacteria cell concentrations (>3 log reduction). Therefore, implementing MAR prior to ozonation appears to remove the bio-amenable compounds that react rapidly with ozone, thereby reducing oxidant demand and treatment efficiency. © 2014 Springer-Verlag Berlin Heidelberg.

Stratospheric ozone: an introduction to its study

International Nuclear Information System (INIS)

Nicolet, M.

1975-01-01

An analysis is made of the various reactions in which ozone and atomic oxygen are involved in the stratosphere. At the present time, hydrogen, nitrogen, and chlorine compounds in the ranges parts per million, parts per billion, and parts per trillion may have significant chemical effects. In the upper stratosphere, above the ozone peak, where there is no strong departure from photochemical equilibrium conditions, the action of hydroxyl and hydroperoxyl radicals of nitrogen dioxide and chlorine monoxide on atomic oxygen and of atomic chlorine on ozone can be introduced. A precise determination of their exact effects requires knowledge of the vertical distribution of the H 2 O, CH 4 , and H 2 dissociation by reaction of these molecules with electronically excited oxygen atom O( 1 D); the ratio of the OH and HO 2 concentrations and their absolute values, which depend on insufficiently known rate coefficients; the various origins of nitric oxide production, with their vertical distributions related to latitude and season; and the various sources giving different chlorine compounds that may be dissociated in the stratosphere. In the lower stratosphere, below the ozone peak, there is no important photochemical production of O 3 , but there exist various possibilities of transport. The predictability of the action of chemical reactions depends strongly on important interactions between OH and HO 2 radicals with CO and NO, respectively, which affect the ratio n(OH)/n(HO 2 ) at the tropopause level; between OH and NO 2 , which lead to the formation of nitric acid with its downward transport toward the troposphere; between NO and HO 2 , which lead to NO 2 and its subsequent photodissociation; between ClO and NO, which also lead to NO 2 and become more important than the reaction of ClO with O; and between Cl and various molecules, such as CH 4 and H 2 , which lead to HCl with its downward transportation toward the troposphere

The Utility of the OMI HCHO and NO2 Data Products in Air Quality Decision- Making Activities

Science.gov (United States)

Duncan, Bryan N.

2010-01-01

We will present three related air quality applications of the OMI HCHO (formaldehyde) and NO2 (nitrogen dioxide) data products, which we us to support mission planning of an OMI-like instrument for the proposed GEO-CAPE satellite that has as one of its objectives to study air quality from space. First, we will discuss a novel and practical application of the data products to the "weight of evidence" in the air quality decision-making process (e.g., State Implementation Plan (SIP)) for a city, region, or state to demonstrate that it is making progress toward attainment of the National Ambient Air Quality Standard (NAAQS) for ozone. Any trend, or lack thereof, in the observed OMI HCHO/NO2, which we use as an air quality indicator, may support that an emission control strategy implemented to reduce ozone is or is not occurring for a metropolitan area. Second, we will discuss how we use variations in the OMI HCHO product as a proxy for variability in the biogenic hydrocarbon, isoprene, which is an important player for the formation of high levels of ozone and the dominant source of HCHO in the eastern U.S. Third, we will discuss the variability of NO2 in the U.S. as indicated by the OMI NO2 product. In addition, we will show the impact of the 2005 hurricanes on pollutant emissions, including those associated with the intensive oil extraction and refining activities, in the Gulf of Mexico region using the OMI NO2 product. The variability of HCHO and NO2 as indicated by OMI helps us to understand changes in the OMI HCHO/NO2 and the implications for ozone formation.

Why do Models Overestimate Surface Ozone in the Southeastern United States?

Science.gov (United States)

Travis, Katherine R.; Jacob, Daniel J.; Fisher, Jenny A.; Kim, Patrick S.; Marais, Eloise A.; Zhu, Lei; Yu, Karen; Miller, Christopher C.; Yantosca, Robert M.; Sulprizio, Melissa P.; Thompson, Anne M.; Wennberg, Paul O.; Crounse, John D.; St Clair, Jason M.; Cohen, Ronald C.; Laughner, Joshua L.; Dibb, Jack E.; Hall, Samuel R.; Ullmann, Kirk; Wolfe, Glenn M.; Pollack, Illana B.; Peischl, Jeff; Neuman, Jonathan A.; Zhou, Xianliang

2018-01-01

Ozone pollution in the Southeast US involves complex chemistry driven by emissions of anthropogenic nitrogen oxide radicals (NOx ≡ NO + NO2) and biogenic isoprene. Model estimates of surface ozone concentrations tend to be biased high in the region and this is of concern for designing effective emission control strategies to meet air quality standards. We use detailed chemical observations from the SEAC4RS aircraft campaign in August and September 2013, interpreted with the GEOS-Chem chemical transport model at 0.25°×0.3125° horizontal resolution, to better understand the factors controlling surface ozone in the Southeast US. We find that the National Emission Inventory (NEI) for NOx from the US Environmental Protection Agency (EPA) is too high. This finding is based on SEAC4RS observations of NOx and its oxidation products, surface network observations of nitrate wet deposition fluxes, and OMI satellite observations of tropospheric NO2 columns. Our results indicate that NEI NOx emissions from mobile and industrial sources must be reduced by 30–60%, dependent on the assumption of the contribution by soil NOx emissions. Upper tropospheric NO2 from lightning makes a large contribution to satellite observations of tropospheric NO2 that must be accounted for when using these data to estimate surface NOx emissions. We find that only half of isoprene oxidation proceeds by the high-NOx pathway to produce ozone; this fraction is only moderately sensitive to changes in NOx emissions because isoprene and NOx emissions are spatially segregated. GEOS-Chem with reduced NOx emissions provides an unbiased simulation of ozone observations from the aircraft, and reproduces the observed ozone production efficiency in the boundary layer as derived from a regression of ozone and NOx oxidation products. However, the model is still biased high by 8±13 ppb relative to observed surface ozone in the Southeast US. Ozonesondes launched during midday hours show a 7 ppb ozone decrease

Why do Models Overestimate Surface Ozone in the Southeastern United States?

Science.gov (United States)

Travis, Katherine R.; Jacob, Daniel J.; Fisher, Jenny A.; Kim, Patrick S.; Marais, Eloise A.; Zhu, Lei; Yu, Karen; Miller, Christopher C.; Yantosca, Robert M.; Sulprizio, Melissa P.;

Total peroxy nitrates and ozone production : analysis of forest fire plumes during BORTAS campaign

Science.gov (United States)

Busilacchio, Marcella; Di Carlo, Piero; Aruffo, Eleonora; Biancofiore, Fabio; Giammaria, Franco; Bauguitte, Stephane; Lee, James; Moller, Sarah; Lewis, Ally; Parrington, Mark; Palmer, Paul; Dari Salisburgo, Cesare

2014-05-01

The goal of this work is to investigate the connection between PNS and ozone within plumes emitted from boreal forest fires and the possible perturbation to oxidant chemistry in the troposphere. During the Aircraft campaign in Canada called BORTAS (summer 2011 ) were carried out several profiles from ground up to 10 km with the BAe-146 aircraft to observe the atmospheric composition inside and outside fire plumes. The BORTAS flights have been selected based on the preliminary studies of 'Plume identification', selecting those effected by Boreal forest fire emissions (CO > 200 ppbv). The FLAMBE fire counts were used concertedly with back trajectory calculations generated by the HYbrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) model to locate the sources of Boreal biomass burning.Profiles measured on board the BAe-146 aircraft are used to calculate the productions of PNs and O3 within the biomass burning plume. By selecting the flights that intercept the biomass burning plume, we evaluate the ratio between the ozone production and the PNs production within the plume. Analyzing this ratio it is possible to determine whether O3 production or PNs production is the dominant process in the biomass burning boreal plume detected during BORTAS campaign.

Evidence for photolytic cycle and transport of NO, NO2 and O3 in the urban air of Beograd

International Nuclear Information System (INIS)

Stamatovic, A.; Markovic, D.; Milekic, Z.; Novakovic, V.

1994-01-01

The first continuous measurements of NO, NO 2 and O 3 concentrations in the urban area of Belgrade were made during the summer-autumn season of 1993. The concentrations of NO and NO 2 have been measured with a Dasibi model 2108 luminescence monitor calibrated via permeation tube. The ozone concentration has been deduced from the total oxidants data obtained from electrochemical cell measurements, calibrated with an ozone generator. Assumed accuracy of both calibration is around 20%. (author)

Effects of a pulsed operation on ozone production in dielectric barrier air discharges

OpenAIRE

Ruggero Barni; Ilaria Biganzoli; Elisa Dell’Orto; Claudia Riccardi

2014-01-01

We have performed an experimental investigation of ozone production in a pulsed dielectric barrier discharge (DBD) reactor. Measurements of ozone in the gas-phase as a function of the power level show that in continuous mode a maximum concentration is achieved before a decrease presumably connected with gas-phase heating. When the reactor is employed in pulsed mode, by applying a definite duty cycle, a strong increase in ozone concentration is generally observed, with a maximum which happens...

The impacts of surface ozone pollution on winter wheat productivity in China--An econometric approach.

Science.gov (United States)

Yi, Fujin; Jiang, Fei; Zhong, Funing; Zhou, Xun; Ding, Aijun

2016-01-01

The impact of surface ozone pollution on winter wheat yield is empirically estimated by considering socio-economic and weather determinants. This research is the first to use an economic framework to estimate the ozone impact, and a unique county-level panel is employed to examine the impact of the increasing surface ozone concentration on the productivity of winter wheat in China. In general, the increment of surface ozone concentration during the ozone-sensitive period of winter wheat is determined to be harmful to its yield, and a conservative reduction of ozone pollution could significantly increase China's wheat supply. Copyright © 2015 Elsevier Ltd. All rights reserved.

Effect of sonically induced deflocculation on the efficiency of ozone mediated partial sludge disintegration for improved production of biogas.

Science.gov (United States)

Sowmya Packyam, G; Kavitha, S; Adish Kumar, S; Kaliappan, S; Yeom, Ick Tae; Rajesh Banu, J

2015-09-01

In this study, ultrasonication was used for sludge deflocculation, followed by cell disintegration using ozone. The effect of this phase separated sono-ozone pretreatment is evaluated based on extra polymeric substances release, deoxyribonucleic acid (DNA) in the medium, solubilization of intra cellular components and suspended solids (SS) reduction. Ultrasonically induced deflocculation was optimized at an energy dosage of 76.4(log 1.88)kJ/kg TS. During cell disintegration (ozone dosage 0.0011 mgO3/mgSS), chemical oxygen demand solubilization (COD) and SS reduction of sonic mediated ozone pretreated sludge were 25.4% and 17.8% comparatively higher than ozone pretreated sludge, respectively. Further, biogas production potential of control (raw), flocculated (ozone pretreated), and deflocculated (sonic mediated ozone pretreated) sludges were observed to be 0.202, 0.535 and 0.637 L/(gVS), respectively. Thus, the phase separated pretreatment at lower ultrasonic specific energy and low dose ozone proved to enhance the anaerobic biodegradability efficiently. Copyright © 2015 Elsevier B.V. All rights reserved.

Dynamics of ozone and nitrogen oxides at Summit, Greenland

NARCIS (Netherlands)

Dam, Van Brie; Helmig, Detlev; Toro, Claudia; Doskey, Paul; Kramer, Louisa; Murray, Keenan; Ganzeveld, Laurens; Seok, Brian

2015-01-01

A multi-year investigation of ozone (O₃) and nitrogen oxides (NO_x) in snowpack interstitial air down to a depth of 2.8 m was conducted at Summit, Greenland, to elucidate mechanisms controlling the production and destruction of these important trace gases within the snow.

Ozone modeling

International Nuclear Information System (INIS)

McIllvaine, C.M.

1994-01-01

Exhaust gases from power plants that burn fossil fuels contain concentrations of sulfur dioxide (SO 2 ), nitric oxide (NO), particulate matter, hydrocarbon compounds and trace metals. Estimated emissions from the operation of a hypothetical 500 MW coal-fired power plant are given. Ozone is considered a secondary pollutant, since it is not emitted directly into the atmosphere but is formed from other air pollutants, specifically, nitrogen oxides (NO), and non-methane organic compounds (NMOQ) in the presence of sunlight. (NMOC are sometimes referred to as hydrocarbons, HC, or volatile organic compounds, VOC, and they may or may not include methane). Additionally, ozone formation Alternative is a function of the ratio of NMOC concentrations to NO x concentrations. A typical ozone isopleth is shown, generated with the Empirical Kinetic Modeling Approach (EKMA) option of the Environmental Protection Agency's (EPA) Ozone Isopleth Plotting Mechanism (OZIPM-4) model. Ozone isopleth diagrams, originally generated with smog chamber data, are more commonly generated with photochemical reaction mechanisms and tested against smog chamber data. The shape of the isopleth curves is a function of the region (i.e. background conditions) where ozone concentrations are simulated. The location of an ozone concentration on the isopleth diagram is defined by the ratio of NMOC and NO x coordinates of the point, known as the NMOC/NO x ratio. Results obtained by the described model are presented

Information content of ozone retrieval algorithms

Science.gov (United States)

Rodgers, C.; Bhartia, P. K.; Chu, W. P.; Curran, R.; Deluisi, J.; Gille, J. C.; Hudson, R.; Mateer, C.; Rusch, D.; Thomas, R. J.

1989-01-01

The algorithms are characterized that were used for production processing by the major suppliers of ozone data to show quantitatively: how the retrieved profile is related to the actual profile (This characterizes the altitude range and vertical resolution of the data); the nature of systematic errors in the retrieved profiles, including their vertical structure and relation to uncertain instrumental parameters; how trends in the real ozone are reflected in trends in the retrieved ozone profile; and how trends in other quantities (both instrumental and atmospheric) might appear as trends in the ozone profile. No serious deficiencies were found in the algorithms used in generating the major available ozone data sets. As the measurements are all indirect in someway, and the retrieved profiles have different characteristics, data from different instruments are not directly comparable.

Pulmonary effects of inhaled limonene ozone reaction products in elderly rats.

Science.gov (United States)

Sunil, Vasanthi R; Laumbach, Robert J; Patel, Kinal J; Turpin, Barbara J; Lim, Ho-Jin; Kipen, Howard M; Laskin, Jeffrey D; Laskin, Debra L

2007-07-15

d-Limonene is an unsaturated volatile organic chemical found in cleaning products, air fresheners and soaps. It is oxidized by ozone to secondary organic aerosols consisting of aldehydes, acids, oxidants and fine and ultra fine particles. The lung irritant effects of these limonene ozone reaction products (LOP) were investigated. Female F344 rats (2- and 18-month-old) were exposed for 3 h to air or LOP formed by reacting 6 ppm d-limonene and 0.8 ppm ozone. BAL fluid, lung tissue and cells were analyzed 0 h and 20 h later. Inhalation of LOP increased TNF-alpha, cyclooxygenase-2, and superoxide dismutase in alveolar macrophages (AM) and Type II cells. Responses of older animals were attenuated when compared to younger animals. LOP also decreased p38 MAP kinase in AM from both younger and older animals. In contrast, while LOP increased p44/42 MAP kinase in AM from younger rats, expression decreased in AM and Type II cells from older animals. NF-kappaB and C/EBP activity also increased in AM from younger animals following LOP exposure but decreased or was unaffected in Type II cells. Whereas in younger animals LOP caused endothelial cell hypertrophy, perivascular and pleural edema and thickening of alveolar septal walls, in lungs from older animals, patchy accumulation of fluid within septal walls in alveolar sacs and subtle pleural edema were noted. LOP are pulmonary irritants inducing distinct inflammatory responses in younger and older animals. This may contribute to the differential sensitivity of these populations to pulmonary irritants.

Pulmonary effects of inhaled limonene ozone reaction products in elderly rats

International Nuclear Information System (INIS)

Sunil, Vasanthi R.; Laumbach, Robert J.; Patel, Kinal J.; Turpin, Barbara J.; Lim, Ho-Jin; Kipen, Howard M.; Laskin, Jeffrey D.; Laskin, Debra L.

2007-01-01

d-Limonene is an unsaturated volatile organic chemical found in cleaning products, air fresheners and soaps. It is oxidized by ozone to secondary organic aerosols consisting of aldehydes, acids, oxidants and fine and ultra fine particles. The lung irritant effects of these limonene ozone reaction products (LOP) were investigated. Female F344 rats (2- and 18-month-old) were exposed for 3 h to air or LOP formed by reacting 6 ppm d-limonene and 0.8 ppm ozone. BAL fluid, lung tissue and cells were analyzed 0 h and 20 h later. Inhalation of LOP increased TNF-α, cyclooxygenase-2, and superoxide dismutase in alveolar macrophages (AM) and Type II cells. Responses of older animals were attenuated when compared to younger animals. LOP also decreased p38 MAP kinase in AM from both younger and older animals. In contrast, while LOP increased p44/42 MAP kinase in AM from younger rats, expression decreased in AM and Type II cells from older animals. NF-κB and C/EBP activity also increased in AM from younger animals following LOP exposure but decreased or was unaffected in Type II cells. Whereas in younger animals LOP caused endothelial cell hypertrophy, perivascular and pleural edema and thickening of alveolar septal walls, in lungs from older animals, patchy accumulation of fluid within septal walls in alveolar sacs and subtle pleural edema were noted. LOP are pulmonary irritants inducing distinct inflammatory responses in younger and older animals. This may contribute to the differential sensitivity of these populations to pulmonary irritants

Influence of local meteorology and NO2 conditions on ground-level ozone concentrations in the eastern part of Texas, USA.

Science.gov (United States)

Gorai, A K; Tuluri, F; Tchounwou, P B; Ambinakudige, S

2015-02-01

The influence of local climatic factors on ground-level ozone concentrations is an area of increasing interest to air quality management in regards to future climate change. This study presents an analysis on the role of temperature, wind speed, wind direction, and NO 2 level on ground-level ozone concentrations over the region of Eastern Texas, USA. Ozone concentrations at the ground level depend on the formation and dispersion processes. Formation process mainly depends on the precursor sources, whereas, the dispersion of ozone depends on meteorological factors. Study results showed that the spatial mean of ground-level ozone concentrations was highly dependent on the spatial mean of NO 2 concentrations. However, spatial distributions of NO 2 and ozone concentrations were not uniformed throughout the study period due to uneven wind speeds and wind directions. Wind speed and wind direction also played a significant role in the dispersion of ozone. Temperature profile in the area rarely had any effects on the ozone concentrations due to low spatial variations.

Why do models overestimate surface ozone in the Southeast United States?

Directory of Open Access Journals (Sweden)

K. R. Travis

2016-11-01

Full Text Available Ozone pollution in the Southeast US involves complex chemistry driven by emissions of anthropogenic nitrogen oxide radicals (NOx  ≡  NO + NO2 and biogenic isoprene. Model estimates of surface ozone concentrations tend to be biased high in the region and this is of concern for designing effective emission control strategies to meet air quality standards. We use detailed chemical observations from the SEAC4RS aircraft campaign in August and September 2013, interpreted with the GEOS-Chem chemical transport model at 0.25°  ×  0.3125° horizontal resolution, to better understand the factors controlling surface ozone in the Southeast US. We find that the National Emission Inventory (NEI for NOx from the US Environmental Protection Agency (EPA is too high. This finding is based on SEAC4RS observations of NOx and its oxidation products, surface network observations of nitrate wet deposition fluxes, and OMI satellite observations of tropospheric NO2 columns. Our results indicate that NEI NOx emissions from mobile and industrial sources must be reduced by 30–60 %, dependent on the assumption of the contribution by soil NOx emissions. Upper-tropospheric NO2 from lightning makes a large contribution to satellite observations of tropospheric NO2 that must be accounted for when using these data to estimate surface NOx emissions. We find that only half of isoprene oxidation proceeds by the high-NOx pathway to produce ozone; this fraction is only moderately sensitive to changes in NOx emissions because isoprene and NOx emissions are spatially segregated. GEOS-Chem with reduced NOx emissions provides an unbiased simulation of ozone observations from the aircraft and reproduces the observed ozone production efficiency in the boundary layer as derived from a regression of ozone and NOx oxidation products. However, the model is still biased high by 6 ± 14 ppb relative to observed surface ozone in the Southeast US. Ozonesondes

Ozone and meteorological boundary-layer conditions at Summit, Greenland, during 3-21 June 2000

Energy Technology Data Exchange (ETDEWEB)

Helmig, D.; Boulter, J.; David, D.; Birks, J.W.; Cullen, N.J.; Steffen, K. [University of Colorado, Boulder, CO (United States). Cooperative Institute for Research in Environmental Sciences; Johnson, B.J.; Oltmans, S.J. [National Oceanic and Atmospheric Administration, Boulder, CO (United States). Climate Monitoring and Diagnostics Laboratory

2002-06-01

The temporal and spatial distributions of boundary-layer ozone were studied during June 2000 at Summit, Greenland, using surface-level measurements and vertical profiling from a tethered balloon platform. Three weeks of continuous ozone surface data, 133 meteorological vertical profile data and 82 ozone vertical profile data sets were collected from the surface to a maximum altitude of 1400 m above ground. The lower atmosphere at Summit was characterized by the prevalence of strong stable conditions with strong surface temperature inversions. These inversions reversed to neutral to slightly unstable conditions between {approx} 9.00 and 18.00 h local time with the formation of shallow mixing heights of {approx} 70-250 m above the surface. The surface ozone mixing ratio ranged from 39 to 68 ppbv and occasionally had rapid changes of up to 20 ppb in 12 h. The diurnal mean ozone mixing ratio showed diurnal trends indicating meteorological and photochemical controls of surface ozone. Vertical profiles were within the range of 37-76 ppb and showed strong stratification in the lower troposphere. A high correlation of high ozone/low water vapor air masses indicated the transport of high tropospheric/low stratospheric air into the lower boundary layer. An {approx} 0.1-3 ppb decline of the ozone mixing ratio towards the surface was frequently observed within the neutrally stable mixed layer during midday hours. These data suggest that the boundary-layer ozone mixing ratio and ozone depletion and deposition to the snowpack are influenced by the boundary-layer ozone mixing ratio and ozone depletion and deposition to the snowpack are influenced by photochemical processes and/or transport phenomena that follow diurnal dependencies. With 37 ppb of ozone being the lowest mixing ratio measured in all data no evidence was seen for the occurrence of ozone depletion episodes similar to those that have been reported within the boundary layer at coastal Arctic sites during springtime

Polar-night O3, NO2 and NO3 distributions during sudden stratospheric warmings in 2003–2008 as seen by GOMOS/Envisat

Directory of Open Access Journals (Sweden)

E. Kyrölä

2012-01-01

Full Text Available Sudden stratospheric warmings (SSW are large-scale transient events, which have a profound effect on the Northern Hemisphere stratospheric circulation in winter. During the SSW events the temperature in stratosphere increases by several tens of Kelvins and zonal winds decelerate or reverse in direction. Changes in temperature and dynamics significantly affect the chemical composition of the middle atmosphere. In this paper, the response of the middle-atmosphere trace gases during several sudden stratospheric warmings in 2003–2008 is investigated using measurements from the GOMOS (Global Ozone Monitoring by Occultation of Stars instrument on board the Envisat satellite. We have analyzed spatial and temporal changes of NO2 and NO3 in the stratosphere, and of ozone in the whole middle atmosphere. To facilitate our analyses, we have used the temperature profiles data from the MLS (Microwave Limb Sounder instrument on board the Aura satellite, as well as simulations by the FinROSE chemistry-transport model and the Sodankylä Ion and Neutral Chemistry model (SIC. NO3 observations in the polar winter stratosphere during SSWs are reported for the first time. Changes in chemical composition are found not to be restricted to the stratosphere, but to extend to mesosphere and lower thermosphere. They often exhibit a complicated structure, because the distribution of trace gases is affected by changes in both chemistry and dynamics. The tertiary ozone maximum in the mesosphere often disappears with the onset of SSW, probably because of strong mixing processes. The strong horizontal mixing with outside-vortex air is well observed also in NO2 data, especially in cases of enhanced NO2 inside the polar vortex before SSW. Almost in all of the considered events, ozone near the secondary maximum decreases with onset of SSW. In both experimental data and FinROSE modelling, ozone changes are positively correlated with temperature changes in the lower stratosphere

Ozone modeling

Energy Technology Data Exchange (ETDEWEB)

McIllvaine, C M

1994-07-01

Exhaust gases from power plants that burn fossil fuels contain concentrations of sulfur dioxide (SO{sub 2}), nitric oxide (NO), particulate matter, hydrocarbon compounds and trace metals. Estimated emissions from the operation of a hypothetical 500 MW coal-fired power plant are given. Ozone is considered a secondary pollutant, since it is not emitted directly into the atmosphere but is formed from other air pollutants, specifically, nitrogen oxides (NO), and non-methane organic compounds (NMOQ) in the presence of sunlight. (NMOC are sometimes referred to as hydrocarbons, HC, or volatile organic compounds, VOC, and they may or may not include methane). Additionally, ozone formation Alternative is a function of the ratio of NMOC concentrations to NO{sub x} concentrations. A typical ozone isopleth is shown, generated with the Empirical Kinetic Modeling Approach (EKMA) option of the Environmental Protection Agency's (EPA) Ozone Isopleth Plotting Mechanism (OZIPM-4) model. Ozone isopleth diagrams, originally generated with smog chamber data, are more commonly generated with photochemical reaction mechanisms and tested against smog chamber data. The shape of the isopleth curves is a function of the region (i.e. background conditions) where ozone concentrations are simulated. The location of an ozone concentration on the isopleth diagram is defined by the ratio of NMOC and NO{sub x} coordinates of the point, known as the NMOC/NO{sub x} ratio. Results obtained by the described model are presented.

Exploring the direct impacts of particulate matter and surface ozone on global crop production

Science.gov (United States)

Schiferl, L. D.; Heald, C. L.

2016-12-01

The current era of rising food demand to feed an increasing population along with expansion of industrialization throughout the globe has been accompanied by deteriorating air quality and an enhancement in agricultural activity. Both air quality and the food supply are vitally important to sustaining human enterprise, and understanding the effects air quality may have on agricultural production is critical. Particulate matter (PM) in the atmosphere decreases the total photosynthetically available radiation (PAR) available to crops through the scattering and absorption of radiation while also increasing the diffuse fraction (DF) of this PAR. Since plants respond positively to a higher DF through the more even distribution of photons to all leaves, the net effect of PM on crop production depends on the magnitudes of these values and the response mechanisms of a specific crop. In contrast, atmospheric ozone always acts to decrease crop production through its phytotoxic properties. While the relationships between ozone and crop production have been readily studied, the effects of PM on crop production and their relative importance compared to ozone is much more uncertain. This study uses the GEOS-Chem chemical transport model linked to the RRTMG radiative transfer model and the DSSAT crop model to explore the impacts of PM and ozone on the globally distributed production of maize, rice, wheat and soybeans. First, we examine how air quality differentially affects total seasonal production by crop and region. Second, we investigate the dependence of simulated production on air quality over different timescales and under varying cloud conditions.

Application of dimensional analysis to ozone production by pulsed streamer discharge in oxygen

Energy Technology Data Exchange (ETDEWEB)

Buntat, Z; Harry, J E; Smith, I R [Department of Electronic and Electrical Engineering, Loughborough University, Loughborough, Leicestershire LE11 3TU (United Kingdom)

2003-07-07

This paper describes the use of dimensional analysis in investigating the effects of the electrical and the discharge configuration parameters on ozone production in oxygen, by means of a pulsed streamer discharge. Ozone destruction factors are taken into account in the model, and predicted results are shown to be in good agreement with experimental findings.

Application of dimensional analysis to ozone production by pulsed streamer discharge in oxygen

CERN Document Server

Buntat, Z; Smith, I R

2003-01-01

This paper describes the use of dimensional analysis in investigating the effects of the electrical and the discharge configuration parameters on ozone production in oxygen, by means of a pulsed streamer discharge. Ozone destruction factors are taken into account in the model, and predicted results are shown to be in good agreement with experimental findings.

Application of dimensional analysis to ozone production by pulsed streamer discharge in oxygen

International Nuclear Information System (INIS)

Buntat, Z; Harry, J E; Smith, I R

2003-01-01

This paper describes the use of dimensional analysis in investigating the effects of the electrical and the discharge configuration parameters on ozone production in oxygen, by means of a pulsed streamer discharge. Ozone destruction factors are taken into account in the model, and predicted results are shown to be in good agreement with experimental findings

Application of dimensional analysis to ozone production by pulsed streamer discharge in oxygen

Science.gov (United States)

Buntat, Z.; Harry, J. E.; Smith, I. R.

2003-07-01

This paper describes the use of dimensional analysis in investigating the effects of the electrical and the discharge configuration parameters on ozone production in oxygen, by means of a pulsed streamer discharge. Ozone destruction factors are taken into account in the model, and predicted results are shown to be in good agreement with experimental findings.

International aspects of restrictions of ozone-depleting substances

Energy Technology Data Exchange (ETDEWEB)

McDonald, S.C.

1989-10-01

This report summarizes international efforts to protect stratospheric ozone. Also included in this report is a discussion of activities in other countries to meet restrictions in the production and use of ozone-depleting substances. Finally, there is a brief presentation of trade and international competitiveness issues relating to the transition to alternatives for the regulated chlorofluorocarbons (CFCs) and halons. The stratosphere knows no international borders. Just as the impact of reduced stratospheric ozone will be felt internationally, so protection of the ozone layer is properly an international effort. Unilateral action, even by a country that produces and used large quantities of ozone-depleting substances, will not remedy the problem of ozone depletion if other countries do not follow suit. 32 refs., 7 tabs.

Elimination of micropollutants and transformation products from a wastewater treatment plant effluent through pilot scale ozonation followed by various activated carbon and biological filters.

Science.gov (United States)

Knopp, Gregor; Prasse, Carsten; Ternes, Thomas A; Cornel, Peter

2016-09-01

Conventional wastewater treatment plants are ineffective in removing a broad range of micropollutants, resulting in the release of these compounds into the aquatic environment, including natural drinking water resources. Ozonation is a suitable treatment process for micropollutant removal, although, currently, little is known about the formation, behavior, and removal of transformation products (TP) formed during ozonation. We investigated the elimination of 30 selected micropollutants (pharmaceuticals, X-ray contrast media, industrial chemicals, and TP) by biological treatment coupled with ozonation and, subsequently, in parallel with two biological filters (BF) or granular activated carbon (GAC) filters. The selected micropollutants were removed to very different extents during the conventional biological wastewater treatment process. Ozonation (specific ozone consumption: 0.87 ± 0.29 gO3 gDOC(-1), hydraulic retention time: 17 ± 3 min) eliminated a large number of the investigated micropollutants. Although 11 micropollutants could still be detected after ozonation, most of these were eliminated in subsequent GAC filtration at bed volumes (BV) of approximately 25,000 m(3) m(-3). In contrast, no additional removal of micropollutants was achieved in the BF. Ozonation of the analgesic tramadol led to the formation of tramadol-N-oxide that is effectively eliminated by GAC filters, but not by BF. For the antiviral drug acyclovir, the formation of carboxy-acyclovir was observed during activated sludge treatment, with an average concentration of 3.4 ± 1.4 μg L(-1) detected in effluent samples. Subsequent ozonation resulted in the complete elimination of carboxy-acyclovir and led to the formation of N-(4-carbamoyl-2-imino-5-oxo imidazolidin)-formamido-N-methoxyacetetic acid (COFA; average concentration: 2.6 ± 1.0 μg L(-1)). Neither the BF nor the GAC filters were able to remove COFA. These results highlight the importance of considering TP in the

Upper tropospheric ozone production from lightning NOx-impacted convection: Smoke ingestion case study from the DC3 campaign

Science.gov (United States)

Apel, E. C.; Hornbrook, R. S.; Hills, A. J.; Blake, N. J.; Barth, M. C.; Weinheimer, A.; Cantrell, C.; Rutledge, S. A.; Basarab, B.; Crawford, J.; Diskin, G.; Homeyer, C. R.; Campos, T.; Flocke, F.; Fried, A.; Blake, D. R.; Brune, W.; Pollack, I.; Peischl, J.; Ryerson, T.; Wennberg, P. O.; Crounse, J. D.; Wisthaler, A.; Mikoviny, T.; Huey, G.; Heikes, B.; O'Sullivan, D.; Riemer, D. D.

2015-03-01

As part of the Deep Convective Cloud and Chemistry (DC3) experiment, the National Science Foundation/National Center for Atmospheric Research (NCAR) Gulfstream-V (GV) and NASA DC-8 research aircraft probed the chemical composition of the inflow and outflow of two convective storms (north storm, NS, south storm, SS) originating in the Colorado region on 22 June 2012, a time when the High Park wildfire was active in the area. A wide range of trace species were measured on board both aircraft including biomass burning (BB) tracers hydrogen cyanide (HCN) and acetonitrile (ACN). Acrolein, a much shorter lived tracer for BB, was also quantified on the GV. The data demonstrated that the NS had ingested fresh smoke from the High Park fire and as a consequence had a higher VOC OH reactivity than the SS. The SS lofted aged fire tracers along with other boundary layer ozone precursors and was more impacted by lightning NOx (LNOx) than the NS. The NCAR master mechanism box model was initialized with measurements made in the outflow of the two storms. The NS and SS were predicted to produce 11 and 14 ppbv of O3, respectively, downwind of the storm over 2 days. Sensitivity tests revealed that the ozone production potential of the SS was highly dependent on LNOx. Normalized excess mixing ratios, ΔX/ΔCO, for HCN and ACN were determined in both the fire plume and the storm outflow and found to be 7.0 ± 0.5 and 2.3 ± 0.5 pptv ppbv-1, respectively, and 1.4 ± 0.3 pptv ppbv-1 for acrolein in the outflow only.

Estimating changes in urban ozone concentrations due to life cycle emissions from hydrogen transportation systems

Science.gov (United States)

Wang, Guihua; Ogden, Joan M.; Chang, Daniel P. Y.

Hydrogen has been proposed as a low polluting alternative transportation fuel that could help improve urban air quality. This paper examines the potential impact of introducing a hydrogen-based transportation system on urban ambient ozone concentrations. This paper considers two scenarios, where significant numbers of new hydrogen vehicles are added to a constant number of gasoline vehicles. In our scenarios hydrogen fuel cell vehicles (HFCVs) are introduced in Sacramento, California at market penetrations of 9% and 20%. From a life cycle analysis (LCA) perspective, considering all the emissions involved in producing, transporting, and using hydrogen, this research compares three hypothetical natural gas to hydrogen pathways: (1) on-site hydrogen production; (2) central hydrogen production with pipeline delivery; and (3) central hydrogen production with liquid hydrogen truck delivery. Using a regression model, this research shows that the daily maximum temperature correlates well with atmospheric ozone formation. However, increases in initial VOC and NO x concentrations do not necessarily increase the peak ozone concentration, and may even cause it to decrease. It is found that ozone formation is generally limited by NO x in the summer and is mostly limited by VOC in the fall in Sacramento. Of the three hydrogen pathways, the truck delivery pathway contributes the most to ozone precursor emissions. Ozone precursor emissions from the truck pathway at 9% market penetration can cause additional 3-h average VOC (or NO x) concentrations up to approximately 0.05% (or 1%) of current pollution levels, and at 20% market penetration up to approximately 0.1% (or 2%) of current pollution levels. However, all of the hydrogen pathways would result in very small (either negative or positive) changes in ozone air quality. In some cases they will result in worse ozone air quality (mostly in July, August, and September), and in some cases they will result in better ozone air quality

Estimating changes in urban ozone concentrations due to life cycle emissions from hydrogen transportation systems

International Nuclear Information System (INIS)

Guihua Wang; Ogden, Joan M.; Chang, Daniel P.Y.

2007-01-01

Hydrogen has been proposed as a low polluting alternative transportation fuel that could help improve urban air quality. This paper examines the potential impact of introducing a hydrogen-based transportation system on urban ambient ozone concentrations. This paper considers two scenarios, where significant numbers of new hydrogen vehicles are added to a constant number of gasoline vehicles. In our scenarios hydrogen fuel cell vehicles (HFCVs) are introduced in Sacramento, California at market penetrations of 9% and 20%. From a life cycle analysis (LCA) perspective, considering all the emissions involved in producing, transporting, and using hydrogen, this research compares three hypothetical natural gas to hydrogen pathways: (1) on-site hydrogen production; (2) central hydrogen production with pipeline delivery; and (3) central hydrogen production with liquid hydrogen truck delivery. Using a regression model, this research shows that the daily maximum temperature correlates well with atmospheric ozone formation. However, increases in initial VOC and NO x concentrations do not necessarily increase the peak ozone concentration, and may even cause it to decrease. It is found that ozone formation is generally limited by NO x in the summer and is mostly limited by VOC in the fall in Sacramento. Of the three hydrogen pathways, the truck delivery pathway contributes the most to ozone precursor emissions. Ozone precursor emissions from the truck pathway at 9% market penetration can cause additional 3-h average VOC (or NO x ) concentrations up to approximately 0.05% (or 1%) of current pollution levels, and at 20% market penetration up to approximately 0.1% (or 2%) of current pollution levels. However, all of the hydrogen pathways would result in very small (either negative or positive) changes in ozone air quality. In some cases they will result in worse ozone air quality (mostly in July, August, and September), and in some cases they will result in better ozone air

Estimation of surface UV levels based on Meteor-3/TOMS ozone data

Energy Technology Data Exchange (ETDEWEB)

Borisov, Y A [Central Aerological Observatory, Moscow (Russian Federation); Geogdzhaev, I V [Moscow Inst. of Physics and Technology, Moscow (Russian Federation); Khattatov, V U [Central Aerological Observatory, Moscow (Russian Federation)

1996-12-31

The major consequence of ozone layer depletion for the environment is an increase of harmful ultraviolet (UV) radiation on the Earth surface and in the upper ocean. This implies the importance of environmental UV monitoring. Since the direct global monitoring is not currently possible, indirect estimations of surface UV levels may be used based on satellite ozone data (Madronich, S. 1992). Total Ozone Mapping Spectrometer (TOMS) on board the METEOR-3 satellite provided regular set of data for such estimates. During the time of its operation (August, 1991 - December, 1994) the instrument registered several ozone hole events over Antarctica, when ozone levels dropped by as much as 60 % from their unperturbed values. Probably even more alarming ozone depletions were observed over highly populated regions of middle latitudes of northern hemisphere. Radiative transfer modeling was used to convert METEOR-3/TOMS daily ozone values into regional and global maps of biologically active UV. Calculations demonstrate the effect on surface UV levels produced by ozone hole over Antarctica and ozone depletions over the territory of Russia (March, 1994). UV contour lines deviate from the normal appearance which is determined by growing southward solar elevation. UV contour lines are almost perpendicular to the ozone ones in the ozone depletions areas. The 30 % ozone depletion, over Siberia caused more than 30 % increase in noontime erythemal UV levels, which is equivalent to 10-15 degrees southward latitude displacement. Higher UV radiation increases were found in ozone hole over South America (October 1992) equivalent to about 20 degrees southward displacement

Estimation of surface UV levels based on Meteor-3/TOMS ozone data

Energy Technology Data Exchange (ETDEWEB)

Borisov, Y.A. [Central Aerological Observatory, Moscow (Russian Federation); Geogdzhaev, I.V. [Moscow Inst. of Physics and Technology, Moscow (Russian Federation); Khattatov, V.U. [Central Aerological Observatory, Moscow (Russian Federation)

1995-12-31

The major consequence of ozone layer depletion for the environment is an increase of harmful ultraviolet (UV) radiation on the Earth surface and in the upper ocean. This implies the importance of environmental UV monitoring. Since the direct global monitoring is not currently possible, indirect estimations of surface UV levels may be used based on satellite ozone data (Madronich, S. 1992). Total Ozone Mapping Spectrometer (TOMS) on board the METEOR-3 satellite provided regular set of data for such estimates. During the time of its operation (August, 1991 - December, 1994) the instrument registered several ozone hole events over Antarctica, when ozone levels dropped by as much as 60 % from their unperturbed values. Probably even more alarming ozone depletions were observed over highly populated regions of middle latitudes of northern hemisphere. Radiative transfer modeling was used to convert METEOR-3/TOMS daily ozone values into regional and global maps of biologically active UV. Calculations demonstrate the effect on surface UV levels produced by ozone hole over Antarctica and ozone depletions over the territory of Russia (March, 1994). UV contour lines deviate from the normal appearance which is determined by growing southward solar elevation. UV contour lines are almost perpendicular to the ozone ones in the ozone depletions areas. The 30 % ozone depletion, over Siberia caused more than 30 % increase in noontime erythemal UV levels, which is equivalent to 10-15 degrees southward latitude displacement. Higher UV radiation increases were found in ozone hole over South America (October 1992) equivalent to about 20 degrees southward displacement

Source attribution of tropospheric ozone

Science.gov (United States)

Butler, T. M.

2015-12-01

Tropospheric ozone is a harmful pollutant with adverse effects on human health and ecosystems. As well as these effects, tropospheric ozone is also a powerful greenhouse gas, with an anthropogenic radiative forcing one quarter of that of CO2. Along with methane and atmospheric aerosol, tropospheric ozone belongs to the so-called Short Lived Climate forcing Pollutants, or SLCP. Recent work has shown that efforts to reduce concentrations of SLCP in the atmosphere have the potential to slow the rate of near-term climate change, while simultaneously improving public health and reducing crop losses. Unlike many other SLCP, tropospehric ozone is not directly emitted, but is instead influenced by two distinct sources: transport of air from the ozone-rich stratosphere; and photochemical production in the troposphere from the emitted precursors NOx (oxides of nitrogen), CO (Carbon Monoxide), and VOC (volatile organic compounds, including methane). Better understanding of the relationship between ozone production and the emissions of its precursors is essential for the development of targeted emission reduction strategies. Several modeling methods have been employed to relate the production of tropospheric ozone to emissions of its precursors; emissions perturbation, tagging, and adjoint sensitivity methods all deliver complementary information about modelled ozone production. Most studies using tagging methods have focused on attribution of tropospheric ozone production to emissions of NOx, even though perturbation methods have suggested that tropospheric ozone is also sensitive to VOC, particularly methane. In this study we describe the implementation into a global chemistry-climate model of a scheme for tagging emissions of NOx and VOC with an arbitrary number of labels, which are followed through the chemical reactions of tropospheric ozone production in order to perform attribution of tropospehric ozone to its emitted precursors. Attribution is performed to both

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

Science.gov (United States)

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

2003-11-01

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

Application of Response Surface Methodology for characterization of ozone production from Multi-Cylinder Reactor in non-thermal plasma device

Science.gov (United States)

Lian See, Tan; Zulazlan Shah Zulkifli, Ahmad; Mook Tzeng, Lim

2018-04-01

Ozone is a reactant which can be applied for various environmental treatment processes. It can be generated via atmospheric air non-thermal plasmas when sufficient voltages are applied through a combination of electrodes and dielectric materials. In this study, the concentration of ozone generated via two different configurations of multi-cylinder dielectric barrier discharge (DBD) reactor (3 x 40 mm and 10 x 10 mm) was investigated. The influence of the voltage and the duty cycle to the concentration of ozone generated by each configuration was analysed using response surface methodology. Voltage was identified as significant factor to the ozone production process. However, the regressed model was biased towards one of the configuration, leaving the predicted results of another configuration to be out of range.

Ketoprofen removal by O3 and O3/UV processes: Kinetics, transformation products and ecotoxicity

International Nuclear Information System (INIS)

Illés, Erzsébet; Szabó, Emese; Takács, Erzsébet; Wojnárovits, László; Dombi, András; Gajda-Schrantz, Krisztina

2014-01-01

Ozonation (O 3 ) and its combination with ultraviolet radiation (O 3 /UV) were used to decompose ketoprofen (KET). Depending on the initial KET concentration, fourteen to fifty time's faster KET degradation was achieved using combined O 3 /UV method compared to simple ozonation. Using both methods, formation of four major aromatic transformation products were observed: 3-(1-hydroxyethyl)benzophenone, 3-(1-hydroperoxyethyl) benzophenone, 1-(3-benzoylphenyl) ethanone and 3-ethylbenzophenone. In the combined treatment the degradation was mainly due to the direct effect of UV light, however, towards the end of the treatment, O 3 highly contributed to the mineralization of small carboxylic acids. High (∼ 90%) mineralization degree was achieved using the O 3 /UV method. Toxicity tests performed using representatives of three trophic levels of the aquatic ecosystems (producers, consumers and decomposers) Pseudokirchneriella subcapitata green algae, Daphnia magna zooplanktons and Vibrio fischeri bacteria showed that under the used experimental conditions the transformation products have significantly higher toxicity towards all the test organisms, than KET itself. The bacteria and the zooplanktons showed higher tolerance to the formed products than algae. The measured toxicity correlates well with the concentration of the aromatic transformation products, therefore longer treatments than needed for complete degradation of KET are strongly suggested, in order to avoid possible impact of aromatic transformation products on the aquatic ecosystem. - Highlights: • Ketoprofen degradation is significantly faster using O 3 /UV compared to ozonation. • The presence of O 3 enhances the overall mineralization. • Formation of four major aromatic by-products was observed. • The main step in the decomposition is the decarboxylation. • Degradation products have higher toxicity than ketoprofen itself

Atmospheric Ozone and Methane in a Changing Climate

Directory of Open Access Journals (Sweden)

Ivar S. A. Isaksen

2014-07-01

Full Text Available Ozone and methane are chemically active climate-forcing agents affected by climate–chemistry interactions in the atmosphere. Key chemical reactions and processes affecting ozone and methane are presented. It is shown that climate-chemistry interactions have a significant impact on the two compounds. Ozone, which is a secondary compound in the atmosphere, produced and broken down mainly in the troposphere and stratosphre through chemical reactions involving atomic oxygen (O, NOx compounds (NO, NO2, CO, hydrogen radicals (OH, HO2, volatile organic compounds (VOC and chlorine (Cl, ClO and bromine (Br, BrO. Ozone is broken down through changes in the atmospheric distribution of the afore mentioned compounds. Methane is a primary compound emitted from different sources (wetlands, rice production, livestock, mining, oil and gas production and landfills.Methane is broken down by the hydroxyl radical (OH. OH is significantly affected by methane emissions, defined by the feedback factor, currently estimated to be in the range 1.3 to 1.5, and increasing with increasing methane emission. Ozone and methane changes are affected by NOx emissions. While ozone in general increase with increases in NOx emission, methane is reduced, due to increases in OH. Several processes where current and future changes have implications for climate-chemistry interactions are identified. It is also shown that climatic changes through dynamic processes could have significant impact on the atmospheric chemical distribution of ozone and methane, as we can see through the impact of Quasi Biennial Oscillation (QBO. Modeling studies indicate that increases in ozone could be more pronounced toward the end of this century. Thawing permafrost could lead to important positive feedbacks in the climate system. Large amounts of organic material are stored in the upper layers of the permafrost in the yedoma deposits in Siberia, where 2 to 5% of the deposits could be organic material

Revised estimates for ozone reduction by shuttle operation

Science.gov (United States)

Potter, A. E.

1978-01-01

Previous calculations by five different modeling groups of the effect of space shuttle operations on the ozone layer yielded an estimate of 0.2 percent ozone reduction for the Northern Hemisphere at 60 launches per year. Since these calculations were made, the accepted rate constant for the reaction between hydroperoxyl and nitric oxide to yield hydroxyl and nitrogen dioxide, HO2 + NO yields OH + NO2, was revised upward by more than an order of magnitude, with a resultant increase in the predicted ozone reduction for chlorofluoromethanes by a factor of approximately 2. New calculations of the shuttle effect were made with use of the new rate constant data, again by five different modeling groups. The new value of the shuttle effect on the ozone layer was found to be 0.25 percent. The increase resulting from the revised rate constant is considerably less for space shuttle operations than for chlorofluoromethane production, because the new rate constant also increases the calculated rate of downward transport of shuttle exhaust products out of the stratosphere.

An optimized two-step derivatization method for analyzing diethylene glycol ozonation products using gas chromatography and mass spectrometry.

Science.gov (United States)

Yu, Ran; Duan, Lei; Jiang, Jingkun; Hao, Jiming

2017-03-01

The ozonation of hydroxyl compounds (e.g., sugars and alcohols) gives a broad range of products such as alcohols, aldehydes, ketones, and carboxylic acids. This study developed and optimized a two-step derivatization procedure for analyzing polar products of aldehydes and carboxylic acids from the ozonation of diethylene glycol (DEG) in a non-aqueous environment using gas chromatography-mass spectrometry. Experiments based on Central Composite Design with response surface methodology were carried out to evaluate the effects of derivatization variables and their interactions on the analysis. The most desirable derivatization conditions were reported, i.e., oximation was performed at room temperature overnight with the o-(2,3,4,5,6-pentafluorobenzyl) hydroxyl amine to analyte molar ratio of 6, silylation reaction temperature of 70°C, reaction duration of 70min, and N,O-bis(trimethylsilyl)-trifluoroacetamide volume of 12.5μL. The applicability of this optimized procedure was verified by analyzing DEG ozonation products in an ultrafine condensation particle counter simulation system. Copyright © 2016. Published by Elsevier B.V.

Two-phase ozonation of chlorinated organics

International Nuclear Information System (INIS)

Bhattacharyya, D.; Freshour, A.; West, D.

1995-01-01

In the last few years the amount of research being conducted in the field of single-phase ozonation has grown extensively. However, traditional aqueous-phase ozonation systems are limited by a lack of selective oxidation potential, low ozone solubility in water, and slow intermediate decomposition rates. Furthermore, ozone may decompose before it can be utilized for pollutant destruction since ozone can be highly unstable in aqueous solutions. Naturally occurring compounds such as NaHCO 3 also affect ozone reactions by inhibiting the formation of OH-free radicals. To compensate for these factors, excess ozone is typically supplied to a reactor. Since ozone generation requires considerable electric power consumption (16 - 24 kWh/kg of O 3 ), attempts to enhance the ozone utilization rate and stability should lead to more efficient application of this process to hazardous waste treatment. To improve the process, ozonation may be more efficiently carried out in a two-phase system consisting of an inert solvent (saturated with O 3 ) contacted with an aqueous phase containing pollutants. The non-aqueous phase must meet the following criteria: (1) non-toxic, (2) very low vapor pressure, (3) high density (for ease of separation), (4) complete insolubility in water, (5) reusability, (6) selective pollutant extractability, (7) high oxidant solubility, and (8) extended O 3 stability. Previously published studies (1) have indicated that a number of fluorinated hydrocarbon compounds fit these criteria. For this project, FC40 (a product of 3M Co.) was chosen due to its low vapor pressure (3 mm Hg) and high specific gravity (1.9). The primary advantages of the FC40 solvent are that it is non-toxic, reusable, has an ozone solubility 10 times that of water, and that 85 % of the ozone remains in the solvent even after 2 hours. This novel two-phase process has been utilized to study the rapid destruction of organic chlorine compounds and organic mixtures

OMI/Aura Ozone (O3) Profile 1-Orbit L2 Swath 13x48km V003

Data.gov (United States)

National Aeronautics and Space Administration — The OMI/Aura Level-2 Ozone Profile data product OMO3PR (Version 003) is now available ( http://disc.gsfc.nasa.gov/Aura/OMI/omo3pr_v003.shtml ) from the NASA Goddard...

Kinetic and Mechanistic Studies for the Gas-phase Reaction of Ozone with 2, 3-Dimethyl-2-Butene and 1, 3-Butadiene

Directory of Open Access Journals (Sweden)

Ismael Abdulsatar AL Mulla

2017-09-01

Full Text Available The reactions of ozone with 2,3-Dimethyl-2-Butene (CH32C=C(CH32 and 1,3-Butadiene CH2=CHCH=CH2 have been investigated under atmospheric conditions at 298±3K in air using both relative and absolute rate techniques, and the measured rate coefficients are found to be in good agreement in both techniques used. The obtained results show the addition of ozone to the double bond in these compounds and how it acts as function of the methyl group substituent situated on the double bond. The yields of all the main products have been determined using FTIR and GC-FID and the product studies of these reactions establish a very good idea for the decomposition pathways for the primary formed compounds (ozonides and give a good information for the effect of the methyl group on the degradation pathways. The results have been discussed from the view point of their importance in the atmospheric oxidation of these pollutants.

A regional scale model for ozone in the United States with subgrid representation of urban and power plant plumes

International Nuclear Information System (INIS)

Sillman, S.; Logan, J.A.; Wofsy, S.C.

1990-01-01

A new approach to modeling regional air chemistry is presented for application to industrialized regions such as the continental US. Rural chemistry and transport are simulated using a coarse grid, while chemistry and transport in urban and power plant plumes are represented by detailed subgrid models. Emissions from urban and power plant sources are processed in generalized plumes where chemistry and dilution proceed for 8-12 hours before mixing with air in a large resolution element. A realistic fraction of pollutants reacts under high-NO x conditions, and NO x is removed significantly before dispersal. Results from this model are compared with results from grid odels that do not distinguish plumes and with observational data defining regional ozone distributions. Grid models with coarse resolution are found to artificially disperse NO x over rural areas, therefore overestimating rural levels of both NO x and O 3 . Regional net ozone production is too high in coarse grid models, because production of O 3 is more efficient per molecule of NO x in the low-concentration regime of rural areas than in heavily polluted plumes from major emission sources. Ozone levels simulated by this model are shown to agree with observations in urban plumes and in rural regions. The model reproduces accurately average regional and peak ozone concentrations observed during a 4-day ozone episode. Computational costs for the model are reduced 25-to 100-fold as compared to fine-mesh models

Using satellite data to guide emission control strategies for surface ozone pollution

Science.gov (United States)

Jin, X.; Fiore, A. M.

2017-12-01

Surface ozone (O3) has adverse effects on public health, agriculture and ecosystems. As a secondary pollutant, ozone is not emitted directly. Ozone forms from two classes of precursors: NOx and VOCs. We use satellite observations of formaldehyde (a marker of VOCs) and NO2 (a marker of NOx) to identify areas which would benefit more from reducing NOx emissions (NOx-limited) versus areas where reducing VOC emissions would lead to lower ozone (VOC-limited). We use a global chemical transport model (GEOS-Chem) to develop a set of threshold values that separate the NOx-limited and VOC-limited conditions. Combining these threshold values with a decadal record of satellite observations, we find that U.S. cities (e.g. New York, Chicago) have shifted from VOC-limited to NOx-limited ozone production regimes in the warm season. This transition reflects the NOx emission controls implemented over the past decade. Increasing NOx sensitivity implies that regional NOx emission control programs will improve O3 air quality more now than it would have a decade ago.

Effect of regional precursor emission controls on long-range ozone transport – Part 1: Short-term changes in ozone air quality

Directory of Open Access Journals (Sweden)

J. J. West

2009-08-01

Full Text Available Observations and models demonstrate that ozone and its precursors can be transported between continents and across oceans. We model the influences of 10% reductions in anthropogenic nitrogen oxide (NO_x emissions from each of nine world regions on surface ozone air quality in that region and all other regions. In doing so, we quantify the relative importance of long-range transport between all source-receptor pairs, for direct short-term ozone changes. We find that for population-weighted concentrations during the three-month "ozone-season", the strongest inter-regional influences are from Europe to the Former Soviet Union, East Asia to Southeast Asia, and Europe to Africa. The largest influences per unit of NO_x reduced, however, are seen for source regions in the tropics and Southern Hemisphere, which we attribute mainly to greater sensitivity to changes in NO_x in the lower troposphere, and secondarily to increased vertical convection to the free troposphere in tropical regions, allowing pollutants to be transported further. Results show, for example, that NO_x reductions in North America are ~20% as effective per unit NO_x in reducing ozone in Europe during summer, as NO_x reductions from Europe itself. Reducing anthropogenic emissions of non-methane volatile organic compounds (NMVOCs and carbon monoxide (CO by 10% in selected regions, can have as large an impact on long-range ozone transport as NO_x reductions, depending on the source region. We find that for many source-receptor pairs, the season of greatest long-range influence does not coincide with the season when ozone is highest in the receptor region. Reducing NO_x emissions in most source regions causes a larger decrease in export of ozone from the source region than in ozone production outside of the source region.

MERRA 3D IAU Tendency, Ozone, Diurnal (1.25x1.25L42) V5.2.0

Data.gov (United States)

National Aeronautics and Space Administration — The MATUCPODT or tavgU_3d_odt_Cp data product is the MERRA Data Assimilation System 3-Dimensional ozone tendencies that is time averaged on pressure levels at a...

Evidence for photolytic cycle and transport of NO, NO{sub 2} and O{sub 3} in the urban air of Beograd

Energy Technology Data Exchange (ETDEWEB)

Stamatovic, A; Markovic, D; Milekic, Z; Novakovic, V [Belgrade Univ. (Yugoslavia)

1994-12-31

The first continuous measurements of NO, NO{sub 2} and O{sub 3} concentrations in the urban area of Belgrade were made during the summer-autumn season of 1993. The concentrations of NO and NO{sub 2} have been measured with a Dasibi model 2108 luminescence monitor calibrated via permeation tube. The ozone concentration has been deduced from the total oxidants data obtained from electrochemical cell measurements, calibrated with an ozone generator. Assumed accuracy of both calibration is around 20%. (author).

Ozone and nitrogen oxides in surface air in Russia: TROICA experiments.

Science.gov (United States)

Pankratova, N.; Elansky, N.; Belikov, I.; Shumskiy, R.

2009-04-01

The results of measurements of surface ozone and nitrogen oxides concentrations over the continental regions of Russia are discussed. The measurements were done during 10 TROICA experiments (Transcontinental Observations Into the Chemistry of the Atmosphere). The TROICA experiment started in 1995. By the present moment ten expeditions along the Trans-Siberian railroad from Moscow to Vladivostok (around 9300 km) are carried out. We separate data sets into unpolluted and polluted areas to study temporal and spatial features. Moreover we analyzed cities (more then 100 cities). About 50% of all data corresponds to unpolluted conditions. The data collected are used in an analysis of the physical and chemical processes occurring over continental Russia. In this work the estimations of seasonal and daily ozone and NOx distribution were made. The seasonal distribution of ozone for TROICA experiments concentration considerably differs from ozone distribution at Mace Head (Ireland) and Hohenpeissenberg (Germany) stations and well agrees with the ozone distribution at Zotino (Russia, East Siberia). The same concerns also a daily variability. The ozone concentration gradient is presented. Ozone concentration gradually increases in the eastward direction. Its result of the air transport from polluted regions of Europe and ozone depletions, oxidations of CH4 in Siberia, forest fires in Siberia and around Baikal Lake, regional transport of burning products from Northern China. Significant factor of ozone increasing is stratospheric-tropospheric exchange. It appears in TROICA-3 experiment. During several hours ozone concentration was more then 60 ppbv. The areas of photochemical ozone generation in polluted air are also detected. We estimate anthropogenic and natural factors, which are responsible for sharp ozone concentration increasing. Acknowledgments. The work was supported by International Science and Technology Center (ISTC) under contract No. 2770 and by Russian Basic

Lethal doses of ozone for control of all stages of internal and external feeders in stored products

DEFF Research Database (Denmark)

Hansen, Lise S.; Hansen, Peer; Jensen, Karl-Martin V.

2012-01-01

Gaseous ozone (O3) has potential for control of insects in stored grain. Previous studies have focused on freely exposed insects. Immatures of internal pests, (e.g. Sitophilus spp. and most stages of Rhyzopertha dominica F.) are protected within kernels and probably require higher doses and....../or longer treatment times for full control. A laboratory study determined the doses of ozone necessary for full control of freely exposed and internal stages of eleven stored product pest species. Test insects were three species of Sitophilus, R. dominica, Tribolium confusum Jacquelin du Val, T. castaneum...

Potential ozone impacts of excess NO2 emissions from diesel particulate filters for on- and off-road diesel engines.

Science.gov (United States)

Bar-llan, Amnon; Johnson, Jeremiah R; Denbleyker, Allison; Chan, Lit-Mian; Yarwood, Gregory; Hitchcock, David; Pinto, Joseph P

2010-08-01

This study considers potential impacts of increased use of diesel oxidation catalysts (DOCs) and catalyzed diesel particulate filters (DPFs) on ozone formation in the Dallas/ Fort Worth (DFW) area. There is concern that excess nitrogen dioxide (NO2) emissions from vehicles equipped with these devices could increase ambient ozone levels. The approach involved developing two scenarios for use of these devices, quantifying excess NO2 emissions in each scenario, and using a photochemical model to estimate the resulting ozone changes. In the "maximum penetration" scenario, DOC/DPF devices in a 2009 fleet of heavy-duty on-road trucks, school buses, and construction equipment were significantly increased by accelerating turnover of these vehicles and equipment to models that would require DOCs/DPFs. In the "realistic" scenario, current fractional usage of these devices was assessed for 2009. For both scenarios, excess NO2 emissions from DOCs/DPFs were estimated using U.S. Environmental Protection Agency's MOBILE6 and NONROAD emissions inventory modeling tools. The emissions analyses were used to adjust the DFW photochemical modeling emissions inventories and the Comprehensive Air Quality Model with extensions air quality model was rerun for the DFW area to determine the impact of these two scenarios on ozone formation. The maximum penetration scenario, which showed an overall reduction in oxides of nitrogen (NO(x)) because of the accelerated turnover of equipment to cleaner models, resulted in a net decrease in daily maximum 8-hr ozone of 4-5 parts per billion (ppb) despite the increase in NO2 emissions. The realistic scenario resulted in a small increase in daily maximum 8-hr ozone of less than 1 ppb for the DFW area. It was concluded that the excess NO2 emissions from DOC/DPF devices result in very small ozone impacts, particularly for the realistic scenario, in the DFW area. There are noticeable decreases in ozone for the maximum penetration scenario because NO

Validation of three different scientific ozone products retrieved from IASI spectra using ozonesondes

Directory of Open Access Journals (Sweden)

G. Dufour

2012-03-01

Full Text Available Three scientific ozone products from the Infrared Atmospheric Sounding Interferometer (IASI aboard MetOp-A, retrieved in three different research teams (LA, LATMOS/ULB, LISA with different retrieval schemes, are characterized and validated using ozonesondes measurements. The characteristics of the products are analyzed in terms of retrieval sensitivity, systematic and random errors, and ability to retrieve the natural variability of ozone and focus on different partial columns from the lower troposphere up to 30 km. The validation covers the midlatitudes and the tropics and the period from January to December 2008. The products present degrees of freedom (DOF in the troposphere between 1 and 1.2 on average in the midlatitudes and between 1 and 1.4 in the tropics. The DOF are distributed differently on the vertical depending on the profiles and the season: summer leading to a better sensitivity to the lower troposphere, as expected. The error estimates range between 10 and 20% from the lower tropospheric partial columns (0–6 km and 0–8 km for the midlatitudes and the tropics respectively to the UTLS partial columns (8–16 km and 11–20 km for the midlatitudes and the tropics respectively for all the products and are about 5% in the stratosphere (16–30 km and for the column up to 30 km. The main feature that arises from the comparison with the ozonesondes is a systematic overestimation of ozone in the UTLS (between 10 and 25% by the three products in the midlatitudes and the tropics, attributed to the moderate vertical resolution of IASI and possibly to spectroscopic inconsistencies. The ability of the products to reproduce natural variability of tropospheric ozone is fairly good and depends on the considered season and region.

Tropospheric Ozone Assessment Report: Database and Metrics Data of Global Surface Ozone Observations

Directory of Open Access Journals (Sweden)

Martin G. Schultz

2017-10-01

Full Text Available In support of the first Tropospheric Ozone Assessment Report (TOAR a relational database of global surface ozone observations has been developed and populated with hourly measurement data and enhanced metadata. A comprehensive suite of ozone data products including standard statistics, health and vegetation impact metrics, and trend information, are made available through a common data portal and a web interface. These data form the basis of the TOAR analyses focusing on human health, vegetation, and climate relevant ozone issues, which are part of this special feature. Cooperation among many data centers and individual researchers worldwide made it possible to build the world's largest collection of 'in-situ' hourly surface ozone data covering the period from 1970 to 2015. By combining the data from almost 10,000 measurement sites around the world with global metadata information, new analyses of surface ozone have become possible, such as the first globally consistent characterisations of measurement sites as either urban or rural/remote. Exploitation of these global metadata allows for new insights into the global distribution, and seasonal and long-term changes of tropospheric ozone and they enable TOAR to perform the first, globally consistent analysis of present-day ozone concentrations and recent ozone changes with relevance to health, agriculture, and climate. Considerable effort was made to harmonize and synthesize data formats and metadata information from various networks and individual data submissions. Extensive quality control was applied to identify questionable and erroneous data, including changes in apparent instrument offsets or calibrations. Such data were excluded from TOAR data products. Limitations of 'a posteriori' data quality assurance are discussed. As a result of the work presented here, global coverage of surface ozone data for scientific analysis has been significantly extended. Yet, large gaps remain in the surface

Spektroskopische (DOAS)-Langzeitmessungen von Ozon und Vorlaeufersubstanzen an der Ostseekuestenstation Arkona. Abschlussbericht; Long term spectroscopic (DOAS) measurement of ozone and related species at the Baltic coast station Arkona. Final report

Energy Technology Data Exchange (ETDEWEB)

Dubois, R [Institut fuer Troposphaerenforschung e.V. (IfT), Leipzig (Germany); Flentje, H [Institut fuer Troposphaerenforschung e.V. (IfT), Leipzig (Germany); Heintz, F [Heidelberg Univ. (Germany). Inst. fuer Umweltphysik; Karbach, H J [Institut fuer Troposphaerenforschung e.V. (IfT), Leipzig (Germany); Stutz, J [Heidelberg Univ. (Germany). Inst. fuer Umweltphysik; Platt, U [Heidelberg Univ. (Germany). Inst. fuer Umweltphysik

1996-08-01

Boundary layer ozone concentrations have been recorded since 1956 by the German Weather Service, (MD / DWD) at Cape Arkona, Island of Ruegen, GDR / FRG. In April 1993, a Long Path Differential Optical Absorption Spectrometer (LP-DOAS) was set up near the DWD-site. Measurements of the concentrations of O{sub 3}, NO{sub 2}, NO{sub 3} and SO{sub 2} were carried out with a newly developed DOAS system. The system incorporates two coaxially arranged Newton-type telescopes, a flat field holographic grating spectrometer and a retro reflector array. Combining the meteorological data with ozone and other gas concentrations, sector-classified results are used to identify the constraints for future evaluations of regional long-term trends of ozone concentrations. A statistical analysis of different trace gases for the periods summer, autumn, winter and spring is prepared. The long term nitrate radicals data record is used to retrieve information on the production rate of nitrate radicals, its lifetime, and possible depletion mechanism. (orig.)

Predicting tropospheric ozone and hydroxyl radical in a global, three-dimensional, chemistry, transport, and deposition model

Energy Technology Data Exchange (ETDEWEB)

Atherton, C.S.

1995-01-05

Two of the most important chemically reactive tropospheric gases are ozone (O{sub 3}) and the hydroxyl radical (OH). Although ozone in the stratosphere is a necessary protector against the sun`s radiation, tropospheric ozone is actually a pollutant which damages materials and vegetation, acts as a respiratory irritant, and is a greenhouse gas. One of the two main sources of ozone in the troposphere is photochemical production. The photochemistry is initiated when hydrocarbons and carbon monoxide (CO) react with nitrogen oxides (NO{sub x} = NO + NO{sub 2}) in the presence of sunlight. Reaction with the hydroxyl radical, OH, is the main sink for many tropospheric gases. The hydroxyl radical is highly reactive and has a lifetime on the order of seconds. Its formation is initiated by the photolysis of tropospheric ozone. Tropospheric chemistry involves a complex, non-linear set of chemical reactions between atmospheric species that vary substantially in time and space. To model these and other species on a global scale requires the use of a global, three-dimensional chemistry, transport, and deposition (CTD) model. In this work, I developed two such three dimensional CTD models. The first model incorporated the chemistry necessary to model tropospheric ozone production from the reactions of nitrogen oxides with carbon monoxide (CO) and methane (CH{sub 4}). The second also included longer-lived alkane species and the biogenic hydrocarbon isoprene, which is emitted by growing plants and trees. The models` ability to predict a number of key variables (including the concentration of O{sub 3}, OH, and other species) were evaluated. Then, several scenarios were simulated to understand the change in the chemistry of the troposphere since preindustrial times and the role of anthropogenic NO{sub x} on present day conditions.

OMI/Aura Ozone (O3) Total Column 1-Orbit L2 Swath 13x24 km V003

Data.gov (United States)

National Aeronautics and Space Administration — The OMI/Aura Level-2 Total Column Ozone Data Product OMTO3 (Version 003) is made available (http://disc.gsfc.nasa.gov/Aura/OMI/omto3_v003.shtml) from the NASA...

Products of Ozone-Initiated Chemistry in a Simulated Aircraft Environment

DEFF Research Database (Denmark)

Wisthaler, Armin; Tamás, Gyöngyi; Wyon, David P.

2005-01-01

We used proton-transfer-reaction mass spectrometry (PTR-MS) to examine the products formed when ozone reacted with the materials in a simulated aircraft cabin, including a loaded high-efficiency particulate air (HEPA) filter in the return air system. Four conditions were examined: cabin (baseline...

The impacts of surface ozone pollution on winter wheat productivity in China – An econometric approach

International Nuclear Information System (INIS)

Yi, Fujin; Jiang, Fei; Zhong, Funing; Zhou, Xun; Ding, Aijun

2016-01-01

The impact of surface ozone pollution on winter wheat yield is empirically estimated by considering socio-economic and weather determinants. This research is the first to use an economic framework to estimate the ozone impact, and a unique county-level panel is employed to examine the impact of the increasing surface ozone concentration on the productivity of winter wheat in China. In general, the increment of surface ozone concentration during the ozone-sensitive period of winter wheat is determined to be harmful to its yield, and a conservative reduction of ozone pollution could significantly increase China's wheat supply. - Highlights: • We examine the impacts of the surface ozone exposure on winter wheat yield in China. • An econometric method is used to measure the ozone impacts. • The results conclude that surface ozone is harmful to winter wheat yield in China. • We confirm that stress conditions such as drought and air particles can mitigate the adverse effect of ozone. - Surface ozone pollution is harmful to winter wheat yield in China by considering socio-economic determinants, weather, and other stress conditions like drought and air particles.

Estonian total ozone climatology

Directory of Open Access Journals (Sweden)

K. Eerme

Full Text Available The climatological characteristics of total ozone over Estonia based on the Total Ozone Mapping Spectrometer (TOMS data are discussed. The mean annual cycle during 1979–2000 for the site at 58.3° N and 26.5° E is compiled. The available ground-level data interpolated before TOMS, have been used for trend detection. During the last two decades, the quasi-biennial oscillation (QBO corrected systematic decrease of total ozone from February–April was 3 ± 2.6% per decade. Before 1980, a spring decrease was not detectable. No decreasing trend was found in either the late autumn ozone minimum or in the summer total ozone. The QBO related signal in the spring total ozone has an amplitude of ± 20 DU and phase lag of 20 months. Between 1987–1992, the lagged covariance between the Singapore wind and the studied total ozone was weak. The spring (April–May and summer (June–August total ozone have the best correlation (coefficient 0.7 in the yearly cycle. The correlation between the May and August total ozone is higher than the one between the other summer months. Seasonal power spectra of the total ozone variance show preferred periods with an over 95% significance level. Since 1986, during the winter/spring, the contribution period of 32 days prevails instead of the earlier dominating 26 days. The spectral densities of the periods from 4 days to 2 weeks exhibit high interannual variability.

Key words. Atmospheric composition and structure (middle atmosphere – composition and chemistry; volcanic effects – Meteorology and atmospheric dynamics (climatology

Environment and health: 3. Ozone depletion and ultraviolet radiation

International Nuclear Information System (INIS)

De Gruijl, F.R.; Van der Leun, J.C.

2000-01-01

Ultraviolet radiation from the sun is responsible for a variety of familiar photochemical reactions, including photochemical smog, bleaching of paints and decay of plastics. Conjugated bonds in organic molecules such as proteins and DNA absorb the UV radiation, which can damage these molecules. By a fortunate evolutionary event, the oxygen produced by photosynthesis forms a filter in the outer reaches of our atmosphere that absorbs the most energetic and harmful UV radiation, with wavelengths below 240 nm (in the UVC band [wavelength 100-280 nm]). In the process, the oxygen molecules split up and recombine to form ozone (Fig. 1). This ratified ozone layer (spread out between 10 and 50 Ion in the stratosphere but only 3 mm thick were it compressed at ground level) in turn efficiently absorbs UV radiation of higher wavelengths (tip to about 310 nm). A part of the UV radiation in the UVB band (wavelength 280-315 nm) still reaches ground level and is absorbed in sufficient amounts to have deleterious effects on cells. The less energetic radiation in the UVA band (wavelength 315-400 nm, bordering the visible band [wavelength 400-800 nm]) is not absorbed by ozone and reaches ground level without much attenuation through a clear atmosphere (i.e., no clouds, no air pollution). Although not completely innocuous, the UVA radiation in sunlight is much less photochemically active and therefore generally less harmful than UVB radiation. Life on earth has adapted itself to the UV stress, particularly UVB stress, fbr example by forming protective UV-absorbing surface layers, by repairing cell damage or by replacing damaged cells entirely. Human skin shows all of these adaptive features. Our eyes are less well adapted, but dicy, are shielded by the brows and by squinting. (author)

Ozone deposition velocities, reaction probabilities and product yields for green building materials

Science.gov (United States)

Lamble, S. P.; Corsi, R. L.; Morrison, G. C.

2011-12-01

Indoor surfaces can passively remove ozone that enters buildings, reducing occupant exposure without an energy penalty. However, reactions between ozone and building surfaces can generate and release aerosols and irritating and carcinogenic gases. To identify desirable indoor surfaces the deposition velocity, reaction probability and carbonyl product yields of building materials considered green (listed, recycled, sustainable, etc.) were quantified. Nineteen separate floor, wall or ceiling materials were tested in a 10 L, flow-through laboratory reaction chamber. Inlet ozone concentrations were maintained between 150 and 200 ppb (generally much lower in chamber air), relative humidity at 50%, temperature at 25 °C and exposure occurred over 24 h. Deposition velocities ranged from 0.25 m h -1 for a linoleum style flooring up to 8.2 m h -1 for a clay based paint; reaction probabilities ranged from 8.8 × 10 -7 to 6.9 × 10 -5 respectively. For all materials, product yields of C 1 thru C 12 saturated n-aldehydes, plus acetone ranged from undetectable to greater than 0.70 The most promising material was a clay wall plaster which exhibited a high deposition velocity (5.0 m h -1) and a low product yield (

Ozone fumigation for safety and quality of wine grapes in postharvest dehydration.

Science.gov (United States)

Botondi, Rinaldo; De Sanctis, Federica; Moscatelli, Niccolò; Vettraino, Anna Maria; Catelli, Cesare; Mencarelli, Fabio

2015-12-01

This paper proposes postharvest ozone fumigation (as a method) to control microorganisms and evaluate the effect on polyphenols, anthocyanins, carotenoids and cell wall enzymes during the grape dehydration for wine production. Pignola grapes were ozone-treated (1.5 g/h) for 18 h (A=shock treatment), then dehydrated or ozone-treated (1.5 g/h) for 18 h and at 0.5 g/h for 4 h each day (B=long-term treatment) during dehydration. Treatment and dehydration were performed at 10 °C. No significant difference was found for total carotenoid, total phenolic and total anthocyanin contents after 18 h of O3 treatment. A significant decrease in phenolic and anthocyanin contents occurred during treatment B. Also carotenoids were affected by B ozone treatment. Pectin methylesterase (PME) and polygalacturonase (PG) activities were higher in A-treated grapes during dehydration. Finally, ozone reduced fungi and yeasts by 50%. Shock ozone fumigation (A treatment) before dehydration can be used to reduce the microbial count during dehydration without affecting polyphenol and carotenoid contents. Copyright © 2015 Elsevier Ltd. All rights reserved.

Tropospheric Ozone Assessment Report: Present-day distribution and trends of tropospheric ozone relevant to climate and global atmospheric chemistry model evaluation

Directory of Open Access Journals (Sweden)

A. Gaudel

2018-05-01

Full Text Available 'The Tropospheric Ozone Assessment Report' (TOAR is an activity of the International Global Atmospheric Chemistry Project. This paper is a component of the report, focusing on the present-day distribution and trends of tropospheric ozone relevant to climate and global atmospheric chemistry model evaluation. Utilizing the TOAR surface ozone database, several figures present the global distribution and trends of daytime average ozone at 2702 non-urban monitoring sites, highlighting the regions and seasons of the world with the greatest ozone levels. Similarly, ozonesonde and commercial aircraft observations reveal ozone’s distribution throughout the depth of the free troposphere. Long-term surface observations are limited in their global spatial coverage, but data from remote locations indicate that ozone in the 21st century is greater than during the 1970s and 1980s. While some remote sites and many sites in the heavily polluted regions of East Asia show ozone increases since 2000, many others show decreases and there is no clear global pattern for surface ozone changes since 2000. Two new satellite products provide detailed views of ozone in the lower troposphere across East Asia and Europe, revealing the full spatial extent of the spring and summer ozone enhancements across eastern China that cannot be assessed from limited surface observations. Sufficient data are now available (ozonesondes, satellite, aircraft across the tropics from South America eastwards to the western Pacific Ocean, to indicate a likely tropospheric column ozone increase since the 1990s. The 2014–2016 mean tropospheric ozone burden (TOB between 60°N–60°S from five satellite products is 300 Tg ± 4%. While this agreement is excellent, the products differ in their quantification of TOB trends and further work is required to reconcile the differences. Satellites can now estimate ozone’s global long-wave radiative effect, but evaluation is difficult due to limited

Ozone-induced airway hyperresponsiveness in patients with asthma: role of neutrophil-derived serine proteinases.

Science.gov (United States)

Hiltermann, T J; Peters, E A; Alberts, B; Kwikkers, K; Borggreven, P A; Hiemstra, P S; Dijkman, J H; van Bree, L A; Stolk, J

1998-04-01

Proteinase inhibitors may be of potential therapeutic value in the treatment of respiratory diseases such as chronic obstructive pulmonary disease (COPD) or asthma. Our aim was to study the role of neutrophils, and neutrophil-derived serine proteinases in an acute model in patients with asthma. Exposure to ozone induces an acute neutrophilic inflammatory reaction accompanied by an increase in airway hyperresponsiveness. It is thought that these two effects of ozone are linked, and that neutrophil-derived serine proteinases (i.e. elastase) may play a role in the ozone-induced airway hyperresponsiveness. Therefore, we examined the effect of recombinant antileukoprotease (rALP), one of the major serine proteinase inhibitors in the lung, on ozone-induced changes in airway hyperresponsiveness in this model. We observed that 16 h after exposure to ozone, airway hyperresponsiveness to methacholine was increased both following placebo and rALP treatment. There was no significant difference between placebo and rALP treatment (change in area under the dose-response curve to methacholine: 117.3+/-59.0 vs 193.6+/-59.6 % fall x DD; p=.12). Moreover, the immediate decrease in FEV1 after ozone exposure was not significantly different between the two groups (placebo: -29.6+/-6.7%; rALP: -20.9+/-3.8%; p=.11). In addition, no significant differences were observed in plasma levels of fibrinogen degradation products generated by neutrophil serine proteinases before and after exposure to ozone. We conclude that neutrophil-derived serine proteinases are not important mediators for ozone-induced hyperresponsiveness.

Urban Summertime Ozone of China: Peak Ozone Hour and Nighttime Mixing

Science.gov (United States)

Qu, H.; Wang, Y.; Zhang, R.

2017-12-01

We investigate the observed diurnal cycle of summertime ozone in the cities of China using a regional chemical transport model. The simulated daytime ozone is in general agreement with the observations. Model simulations suggest that the ozone peak time and peak concentration are a function of NOx (NO + NO2) and volatile organic compound (VOC) emissions. The differences between simulated and observed ozone peak time and peak concentration in some regions can be applied to understand biases in the emission inventories. For example, the VOCs emissions are underestimated over the Pearl River Delta (PRD) region, and either NOx emissions are underestimated or VOC emissions are overestimated over the Yangtze River Delta (YRD) regions. In contrast to the general good daytime ozone simulations, the simulated nighttime ozone has a large low bias of up to 40 ppbv. Nighttime ozone in urban areas is sensitive to the nocturnal boundary-layer mixing, and enhanced nighttime mixing (from the surface to 200-500 m) is necessary for the model to reproduce the observed level of ozone.

Ozone pollution and ozone biomonitoring in European cities Part II. Ozone-induced plant injury and its relationship with descriptors of ozone pollution

DEFF Research Database (Denmark)

Klumpp, A.; Ansel, W.; Klumpp, G.

2006-01-01

within local networks were relatively small, but seasonal and inter-annual differences were strong due to the variability of meteorological conditions and related ozone concentrations. The 2001 data revealed a significant relationship between foliar injury degree and various descriptors of ozone...... pollution such as mean value, AOT20 and AOT40. Examining individual sites of the local monitoring networks separately, however, yielded noticeable differences. Some sites showed no association between ozone pollution and ozone-induced effects, whereas others featured almost linear relationships...

Assessment and Applications of NASA Ozone Data Products Derived from Aura OMI-MLS Satellite Measurements in Context of the GMI Chemical Transport Model

Science.gov (United States)

Ziemke, J. R.; Olsen, M. A.; Witte, J. C.; Douglass, A. R.; Strahan, S. E.; Wargan, K.; Liu, X.; Schoeberl, M. R.; Yang, K.; Kaplan, T. B.;

Enhanced pharmaceutical removal from water in a three step bio-ozone-bio process.

Science.gov (United States)

de Wilt, Arnoud; van Gijn, Koen; Verhoek, Tom; Vergnes, Amber; Hoek, Mirit; Rijnaarts, Huub; Langenhoff, Alette

2018-07-01

Individual treatment processes like biological treatment or ozonation have their limitations for the removal of pharmaceuticals from secondary clarified effluents with high organic matter concentrations (i.e. 17 mg TOC/L). These limitations can be overcome by combining these two processes for a cost-effective pharmaceutical removal. A three-step biological-ozone-biological (BO 3 B) treatment process was therefore designed for the enhanced pharmaceutical removal from wastewater effluent. The first biological step removed 38% of ozone scavenging TOC, thus proportionally reducing the absolute ozone input for the subsequent ozonation. Complementariness between biological and ozone treatment, i.e. targeting different pharmaceuticals, resulted in cost-effective pharmaceutical removal by the overall BO 3 B process. At a low ozone dose of 0.2 g O 3 /g TOC and an HRT of 1.46 h in the biological reactors, the removal of 8 out of 9 pharmaceuticals exceeded 85%, except for metoprolol (60%). Testing various ozone doses and HRTs revealed that pharmaceuticals were ineffectively removed at 0.1 g O3/g TOC and an HRT of 0.3 h. At HRTs of 0.47 and 1.46 h easily and moderately biodegradable pharmaceuticals such as caffeine, gemfibrozil, ibuprofen, naproxen and sulfamethoxazole were over 95% removed by biological treatment. The biorecalcitrant carbamazepine was completely ozonated at a dose of 0.4 g O 3 /g TOC. Ozonation products are likely biodegraded in the last biological reactor as a 17% TOC removal was found. No appreciable acute toxicity towards D. magna, P. subcapitata and V. fischeri was found after exposure to the influents and effluents of the individual BO 3 B reactors. The BO 3 B process is estimated to increase the yearly wastewater treatment tariff per population equivalent in the Netherlands by less than 10%. Overall, the BO 3 B process is a cost-effective treatment process for the removal of pharmaceuticals from secondary clarified effluents. Copyright

Proposed standardized definitions for vertical resolution and uncertainty in the NDACC lidar ozone and temperature algorithms - Part 2: Ozone DIAL uncertainty budget

Science.gov (United States)

Leblanc, Thierry; Sica, Robert J.; van Gijsel, Joanna A. E.; Godin-Beekmann, Sophie; Haefele, Alexander; Trickl, Thomas; Payen, Guillaume; Liberti, Gianluigi

2016-08-01

A standardized approach for the definition, propagation, and reporting of uncertainty in the ozone differential absorption lidar data products contributing to the Network for the Detection for Atmospheric Composition Change (NDACC) database is proposed. One essential aspect of the proposed approach is the propagation in parallel of all independent uncertainty components through the data processing chain before they are combined together to form the ozone combined standard uncertainty. The independent uncertainty components contributing to the overall budget include random noise associated with signal detection, uncertainty due to saturation correction, background noise extraction, the absorption cross sections of O3, NO2, SO2, and O2, the molecular extinction cross sections, and the number densities of the air, NO2, and SO2. The expression of the individual uncertainty components and their step-by-step propagation through the ozone differential absorption lidar (DIAL) processing chain are thoroughly estimated. All sources of uncertainty except detection noise imply correlated terms in the vertical dimension, which requires knowledge of the covariance matrix when the lidar signal is vertically filtered. In addition, the covariance terms must be taken into account if the same detection hardware is shared by the lidar receiver channels at the absorbed and non-absorbed wavelengths. The ozone uncertainty budget is presented as much as possible in a generic form (i.e., as a function of instrument performance and wavelength) so that all NDACC ozone DIAL investigators across the network can estimate, for their own instrument and in a straightforward manner, the expected impact of each reviewed uncertainty component. In addition, two actual examples of full uncertainty budget are provided, using nighttime measurements from the tropospheric ozone DIAL located at the Jet Propulsion Laboratory (JPL) Table Mountain Facility, California, and nighttime measurements from the JPL

Future emission scenarios for chemicals that may deplete stratospheric ozone

International Nuclear Information System (INIS)

Hammitt, J.K; Camm, Frank; Mooz, W.E.; Wolf, K.A.; Bamezai, Anil; Connel, P.S.; Wuebbles, D.J.

1990-01-01

Scenarios are developed for long-term future emissions of seven of the most important manmade chemicals that may deplete ozone and the corresponding effect on stratospheric ozone concentrations is calculated using a one-dimensional atmospheric model. The scenarios are based on detailed analysis of the markets for products that use these chemicals and span a central 90% probability interval for the chemicals joint effect on calculated ozone abundance, assuming no additional regulations. (author). 22 refs., 2 figs., 5 tabs

Physiological studies on photochemical oxidant injury in rice plants. IV. Effect of nitrogen application on endogenous abscisic acid (ABA) production and ozone injury of rice plants

Energy Technology Data Exchange (ETDEWEB)

Jeong, Y.H.; Ota, Y.

1981-12-01

In order to determine the effects of nitrogen application on ABA content of rice plants and their ozone-sensitivity, ABA production and ozone injuries were observed under different levels of nitrogen application with two Japonica and two Japonica X Indica type varieties. In all varieties, endogenous ABA content decreased with the increasing level of nitrogen applied, although total nitrogen content increased with the increasing level of nitrogen applied. Ozone injury was found with increasing level of nitrogen applied and to change depending on the varieties. Ozone injury was found to be more serious with increasing nitrogen content in Jinheung and Nongback, however it was less pronounced in Tongil and Milyang No. 23. Endogenous ABA content and ozone-sensitivity were related to the nitrogen content in the rice plants.

Physiological studies on photochemical oxidant injury in rice plants. II. Effect of abscisic acid (ABA) on ozone injury and ethylene production in rice plants

Energy Technology Data Exchange (ETDEWEB)

Jeong, Y.H.; Nakamura, H.; Ota, Y.

1981-12-01

In order to determine the effect of ABA on ozone injury to rice plants, ethylene production, rate of chlorophyll retention and ozone-sensitivity of rice plants pretreated with ABA solution were investigated. The experiments were carried out in pots using rice plants at the 7-8 leaf stage. The results obtained are summarized as follows: ethylene production by the leaf blades exposed to ozone increased with the increase in the dosage of ozone; ethylene production was higher in cv. Nihonbare which was more sensitive to ozone than in cv. Tongil; pre-treatment with ABA solution one hour before ozone treatment reduced ethylene production by the leaf blades exposed to ozone; and the rate of chlorophyll retention decreased following injury, but increased remarkably by the pre-treatment with ABA solution. In conclusion, it could be demonstrated that ozone injury of rice plants can be reduced by the pre-treatment with ABA solution. 28 references, 5 figures, 1 table.

Ozone from fireworks: Chemical processes or measurement interference?

Science.gov (United States)

Xu, Zheng; Nie, Wei; Chi, Xuguang; Huang, Xin; Zheng, Longfei; Xu, Zhengning; Wang, Jiaping; Xie, Yuning; Qi, Ximeng; Wang, Xinfeng; Xue, Likun; Ding, Aijun

2018-08-15

Fireworks have been identified as one ozone source by photolyzing NO 2 or O 2 and are believed to potentially be important for the nighttime ozone during firework events. In this study, we conducted both lab and field experiments to test two types of fireworks with low and high energy with the goal to distinguish whether the visible ozone signal during firework displays is real. The results suggest that previous understanding of the ozone formation mechanism during fireworks is misunderstood. Ultraviolet ray (UV)-based ozone monitors are interfered by aerosols and some specific VOCs. High-energy fireworks emit high concentrations of particular matters and low VOCs that the artificial ozone can be easily removed by an aerosol filter. Low-energy fireworks emit large amounts of VOCs mostly from the combustion of the cardboard from fireworks that largely interferes with the ozone monitor. Benzene and phenol might be major contributors to the artificial ozone signal. We further checked the nighttime ozone concentration in Jinan and Beijing, China, during Chinese New Year, a period with intense fireworks. A signal of 3-8ppbv ozone was detected and positively correlated to NO and SO 2 , suggesting a considerable influence of these chemicals in interfering with ambient ozone monitoring. Copyright © 2018 Elsevier B.V. All rights reserved.

Emission characteristics of VOCs emitted from consumer and commercial products and their ozone formation potential.

Science.gov (United States)

Dinh, Trieu-Vuong; Kim, Su-Yeon; Son, Youn-Suk; Choi, In-Young; Park, Seong-Ryong; Sunwoo, Young; Kim, Jo-Chun

2015-06-01

The characteristics of volatile organic compounds (VOCs) emitted from several consumer and commercial products (body wash, dishwashing detergent, air freshener, windshield washer fluid, lubricant, hair spray, and insecticide) were studied and compared. The spray products were found to emit the highest amount of VOCs (~96 wt%). In contrast, the body wash products showed the lowest VOC contents (~1.6 wt%). In the spray products, 21.6-96.4 % of the VOCs were propane, iso-butane, and n-butane, which are the components of liquefied petroleum gas. Monoterpene (C10H16) was the dominant component of the VOCs in the non-spray products (e.g., body wash, 53-88 %). In particular, methanol was present with the highest amount of VOCs in windshield washer fluid products. In terms of the number of carbon, the windshield washer fluids, lubricants, insecticides, and hair sprays comprised >95 % of the VOCs in the range C2-C5. The VOCs in the range C6-C10 were predominantly found in the body wash products. The dishwashing detergents and air fresheners contained diverse VOCs from C2 to C11. Besides comprising hazardous VOCs, VOCs from consumer products were also ozone precursors. The ozone formation potential of the consumer and commercial spray products was estimated to be higher than those of liquid and gel materials. In particular, the hair sprays showed the highest ozone formation potential.

OMI/Aura Ozone (O3) Total Column Daily L2 Global 0.25 deg Lat/Lon Grid V003

Data.gov (United States)

National Aeronautics and Space Administration — The OMI/Aura Level-2G Total Column Ozone Data Product OMTO3G (Version 003) is made available ( http://disc.gsfc.nasa.gov/Aura/OMI/omto3g_v003.shtml ) from the NASA...

Quality assessment of the Ozone_cci Climate Research Data Package (release 2017) - Part 1: Ground-based validation of total ozone column data products

Science.gov (United States)

Garane, Katerina; Lerot, Christophe; Coldewey-Egbers, Melanie; Verhoelst, Tijl; Elissavet Koukouli, Maria; Zyrichidou, Irene; Balis, Dimitris S.; Danckaert, Thomas; Goutail, Florence; Granville, Jose; Hubert, Daan; Keppens, Arno; Lambert, Jean-Christopher; Loyola, Diego; Pommereau, Jean-Pierre; Van Roozendael, Michel; Zehner, Claus

2018-03-01

The GOME-type Total Ozone Essential Climate Variable (GTO-ECV) is a level-3 data record, which combines individual sensor products into one single cohesive record covering the 22-year period from 1995 to 2016, generated in the frame of the European Space Agency's Climate Change Initiative Phase II. It is based on level-2 total ozone data produced by the GODFIT (GOME-type Direct FITting) v4 algorithm as applied to the GOME/ERS-2, OMI/Aura, SCIAMACHY/Envisat and GOME-2/Metop-A and Metop-B observations. In this paper we examine whether GTO-ECV meets the specific requirements set by the international climate-chemistry modelling community for decadal stability long-term and short-term accuracy. In the following, we present the validation of the 2017 release of the Climate Research Data Package Total Ozone Column (CRDP TOC) at both level 2 and level 3. The inter-sensor consistency of the individual level-2 data sets has mean differences generally within 0.5 % at moderate latitudes (±50°), whereas the level-3 data sets show mean differences with respect to the OMI reference data record that span between -0.2 ± 0.9 % (for GOME-2B) and 1.0 ± 1.4 % (for SCIAMACHY). Very similar findings are reported for the level-2 validation against independent ground-based TOC observations reported by Brewer, Dobson and SAOZ instruments: the mean bias between GODFIT v4 satellite TOC and the ground instrument is well within 1.0 ± 1.0 % for all sensors, the drift per decade spans between -0.5 % and 1.0 ± 1.0 % depending on the sensor, and the peak-to-peak seasonality of the differences ranges from ˜ 1 % for GOME and OMI to ˜ 2 % for SCIAMACHY. For the level-3 validation, our first goal was to show that the level-3 CRDP produces findings consistent with the level-2 individual sensor comparisons. We show a very good agreement with 0.5 to 2 % peak-to-peak amplitude for the monthly mean difference time series and a negligible drift per decade of the differences in the Northern Hemisphere

Non-target screening to trace ozonation transformation products in a wastewater treatment train including different post-treatments.

Science.gov (United States)

Schollée, Jennifer E; Bourgin, Marc; von Gunten, Urs; McArdell, Christa S; Hollender, Juliane

2018-05-25

Ozonation and subsequent post-treatments are increasingly implemented in wastewater treatment plants (WWTPs) for enhanced micropollutant abatement. While this technology is effective, micropollutant oxidation leads to the formation of ozonation transformation products (OTPs). Target and suspect screening provide information about known parent compounds and known OTPs, but for a more comprehensive picture, non-target screening is needed. Here, sampling was conducted at a full-scale WWTP to investigate OTP formation at four ozone doses (2, 3, 4, and 5 mg/L, ranging from 0.3 to 1.0 gO 3 /gDOC) and subsequent changes during five post-treatment steps (i.e., sand filter, fixed bed bioreactor, moving bed bioreactor, and two granular activated carbon (GAC) filters, relatively fresh and pre-loaded). Samples were measured with online solid-phase extraction coupled to liquid chromatography high-resolution tandem mass spectrometry (LC-HRMS/MS) using electrospray ionization (ESI) in positive and negative modes. Existing non-target screening workflows were adapted to (1) examine the formation of potential OTPs at four ozone doses and (2) compare the removal of OTPs among five post-treatments. In (1), data processing included principal component analysis (PCA) and chemical knowledge on possible oxidation reactions to prioritize non-target features likely to be OTPs. Between 394 and 1328 unique potential OTPs were detected in positive ESI for the four ozone doses tested; between 12 and 324 unique potential OTPs were detected in negative ESI. At a specific ozone dose of 0.5 gO 3 /gDOC, 27 parent compounds were identified and were related to 69 non-target features selected as potential OTPs. Two OTPs were confirmed with reference standards (venlafaxine N-oxide and chlorothiazide); 34 other potential OTPs were in agreement with literature data and/or reaction mechanisms. In (2), hierarchical cluster analysis (HCA) was applied on profiles detected in positive ESI mode across the

Inhibition of DNA replication by ozone in Chinese Hamster V79 cells

International Nuclear Information System (INIS)

Rasmussen, R.E.

1986-01-01

DNA replication in Chinese hamster lung fibroblasts, line V79, was depressed in a dose-dependent manner over an ozone concentration range of 1-10 ppm. When the cells were exposed for 1 h at concentrations up to 6 ppm, the rate of DNA replication, as measured by [ 3 H]thymidine incorporation, declined further during a 3-h period immediately following exposure. At higher ozone concentrations, at which more than 99.9% of the cells were killed, no further decline in DNA replication was seen beyond that immediately following exposure. Cultures exposed for 1 h to 10 mM ethyl methanesulfonate or to 10 J/m 2 of ultraviolet (UV) light showed a similar progressive decline in the rate of DNA replication. The inhibition of DNA replication by ozone resembled that seen after exposure of cells to chemical mutagens or radiation and did not resemble the inhibition produced by metabolic poisons. The results may indicate that ozone or its reaction products interact directly with DNA in a way that inhibits replication

Evaluation of ozonation technique for pesticide residue removal and its effect on ascorbic acid, cyanidin-3-glucoside, and polyphenols in apple (Malus domesticus) fruits.

Science.gov (United States)

Swami, Saurabh; Muzammil, Raunaq; Saha, Supradip; Shabeer, Ahammed; Oulkar, Dasharath; Banerjee, Kaushik; Singh, Shashi Bala

2016-05-01

Ozonated water dip technique was evaluated for the detoxification of six pesticides, i.e., chlorpyrifos, cypermethrin, azoxystrobin, hexaconazole, methyl parathion, and chlorothalonil from apple fruits. Results revealed that ozonation was better than washing alone. Ozonation for 15 min decreased residues of the test pesticides in the range of from 26.91 to 73.58%, while ozonation for 30 min could remove the pesticide residues by 39.39-95.14 % compared to 19.05-72.80 % by washing. Cypermethrin was the least removed pesticide by washing as well as by ozonation. Chlorothalonil, chlorpyrifos, and azoxystrobin were removed up to 71.45-95.14 % in a 30-min ozonation period. In case of methyl parathion removal, no extra advantage could be obtained by ozonation. The HPLC analysis indicated that ozonation also affected adversely the ascorbic acid and cyanidin-3-glucoside content of apples. However, 11 polyphenols studied showed a mixed trend. Gallic acid, 3,4-dihydroxybenzoic acid, catechin, epicatechin, p-coumaric acid, quercetin-3-O-glucoside, quercetin, and kaempferol were found to decrease while syringic acid, rutin, and resveratrol were found to increase in 30-min ozonation.

Convection links biomass burning to increased tropical ozone: However, models will tend to overpredict O3

Science.gov (United States)

Chatfield, Robert B.; Delany, Anthony C.

1990-10-01

Biomass burning throughout the inhabited portions of the tropics generates precursors which lead to significant local atmospheric ozone pollution. Several simulations show how this smog could be only an easily observed, local manifestation of a much broader increase in tropospheric ozone. We illustrate basic processes with a one-dimensional time-dependent model that is closer to true meteorological motions than commonly used eddy diffusion models. Its application to a representative region of South America gives reasonable simulations of the local pollutants measured there. Three illustrative simulations indicate the importance of dilution, principally due to vertical transport, in increasing the efficiency of ozone production, possibly enough for high ozone to be apparent on a very large, intercontinental scale. In the first, cook-then-mix, simulation the nitrogen oxides and other burning-produced pollutants are confined to a persistently subsident fair weather boundary layer for several days, and the resultant ozone is found to have only a transient influence on the whole column of tropospheric ozone. In the second, mix-then-cook, simulation the effect of typical cumulonimbus convection, which vents an actively polluted boundary layer, is to make a persistent increase in the tropical ozone column. Such a broadly increased ozone column is observed over the the populated "continental" portion of the tropics. A third simulation averages all emission, transport, and deposition parameters, representing one column in a global tropospheric model that does not simulate individual weather events. This "oversmoothing" simulation produces 60% more ozone than observed or otherwise modeled. Qualitatively similar overprediction is suggested for all models which average significantly in time or space, as all need do. Clearly, simulating these O3 levels will depend sensitively on knowledge of the timing of emissions and transport.

Chemical composition of gas-phase organic carbon emissions from motor vehicles and implications for ozone production.

Science.gov (United States)

Gentner, Drew R; Worton, David R; Isaacman, Gabriel; Davis, Laura C; Dallmann, Timothy R; Wood, Ezra C; Herndon, Scott C; Goldstein, Allen H; Harley, Robert A

2013-10-15

Motor vehicles are major sources of gas-phase organic carbon, which includes volatile organic compounds (VOCs) and other compounds with lower vapor pressures. These emissions react in the atmosphere, leading to the formation of ozone and secondary organic aerosol (SOA). With more chemical detail than previous studies, we report emission factors for over 230 compounds from gasoline and diesel vehicles via two methods. First we use speciated measurements of exhaust emissions from on-road vehicles in summer 2010. Second, we use a fuel composition-based approach to quantify uncombusted fuel components in exhaust using the emission factor for total uncombusted fuel in exhaust together with detailed chemical characterization of liquid fuel samples. There is good agreement between the two methods except for products of incomplete combustion, which are not present in uncombusted fuels and comprise 32 ± 2% of gasoline exhaust and 26 ± 1% of diesel exhaust by mass. We calculate and compare ozone production potentials of diesel exhaust, gasoline exhaust, and nontailpipe gasoline emissions. Per mass emitted, the gas-phase organic compounds in gasoline exhaust have the largest potential impact on ozone production with over half of the ozone formation due to products of incomplete combustion (e.g., alkenes and oxygenated VOCs). When combined with data on gasoline and diesel fuel sales in the U.S., these results indicate that gasoline sources are responsible for 69-96% of emissions and 79-97% of the ozone formation potential from gas-phase organic carbon emitted by motor vehicles.

Space nuclear power requirements for ozone layer modification

International Nuclear Information System (INIS)

Dolan, T.J.

1991-01-01

This work estimates the power requirements for using photochemical processes driven by space nuclear power to counteract the Earth's ozone layer depletion. The total quantity of ozone (O 3 ) in the Earth's atmosphere is estimated to be about 4.7 x 10 37 molecules. The ozone production and destruction rates in the stratosphere are both on the order of 4.9 x 10 31 molecules/s, differing by a small fraction so that the net depletion rate is about 0.16 to 0.26% per year. The delivered optical power requirement for offsetting this depletion is estimated to be on the order of 3 GW. If the power were produced by satellite reactors at 800 km altitude (orbit decay time ∼ 300 years), some means of efficient power beaming would be needed to deliver the power to stratospheric levels (10--50 km). Ultraviolet radiation at 140--150 nm could have higher absorption rates in O 2 (leading to production of atomic oxygen, which can combine with O 2 to form O 3 ) than in ozone (leading to photodissociation of O 3 ). Potential radiation sources include H 2 lasers and direct nuclear pumping of ultraviolet fluorescers. 5 refs

Disinfection technology with ozone for cryptosporidium; Cryptosporidium taisaku to shite no ozone shodoku gijutsu

Energy Technology Data Exchange (ETDEWEB)

Tanaka, Y.; Takahashi, K. [Fuji Electric Co. Ltd., Tokyo (Japan); Motoyama, N. [Fuji Electric Corporate Research and Development, Ltd., Kanagawa (Japan)

1998-06-10

Measures against Cryptosporidium parvum (C. parvum) in the waterworks are discussed. C. parvum is a pathogenic protozoan, and exists in the form of oocyst protected by a hard shell. It does not multiply in water or food, but does in human intestines and causes violent diarrhea and bellyache. A grave concern was created when many people were infected with the protozoan via tap water in Japan and the United States. Under such circumstances, ozone is used in an experiment to inactivate C. parvum. It is found that the C. parvum oocyst inactivation effect is evaluated by using a Ct value (disinfectant concentration Cmg/Ltimescontact time in minute) and that ozone treatment inactivates 90-99% of the protozoan. When various advanced water treatment technologies are being introduced for the purpose of serving safe and tasty water, the outcome of this study conveniently offers an ozone treatment method that will additionally inactivate pathogenic protozoa. Studies will be continued to elucidate the effects of factors of ozone treatment and water quality for the completion of an ideal disinfection process. Reference is made to an example of disinfection work implemented at a water purification plant of Milwaukie City, United States. 9 refs., 6 figs., 4 tabs.

Suitability of Nicotiana tabacum 'Bel W3' for biomonitoring ozone in Sao Paulo, Brazil

International Nuclear Information System (INIS)

Sant'Anna, Silvia M.R.; Esposito, Marisia P.; Domingos, Marisa; Souza, Silvia R.

2008-01-01

Nicotiana tabacum 'Bel W3' is a widely used sensitive bioindicator for ambient ozone, but it is rarely used in tropical countries. Our goal was to determine the suitability of this plant for biomonitoring ozone in the city of Sao Paulo by evaluating the relationships between leaf necroses and ozone under field conditions and measurements of chlorophyll a fluorescence and antioxidants in plants exposed to different concentrations of ozone in closed chambers. While a weak linear relationship between leaf injury and ozone concentrations (R 2 = 0.10) was determined in the field, a strong linear relationship was observed in the chamber experiments. Maximum leaf injury was observed in plants submitted to 40 ppb, which coincided with a significant decrease in fluorescence and total ascorbic acid. The relationship between leaf damage observed in the field and ozone was improved when the concentrations were limited to 40 ppb (R 2 = 0.28). - Nicotiana tabacum 'Bel W3' is suitable for indicating low ozone levels in Brazil

Influence of corona discharge on the ozone budget in the tropical free troposphere: a case study of deep convection during GABRIEL

Science.gov (United States)

Bozem, H.; Fischer, H.; Gurk, C.; Schiller, C. L.; Parchatka, U.; Koenigstedt, R.; Stickler, A.; Martinez, M.; Harder, H.; Kubistin, D.; Williams, J.; Eerdekens, G.; Lelieveld, J.

2014-09-01

Convective redistribution of ozone and its precursors between the boundary layer (BL) and the free troposphere (FT) influences photochemistry, in particular in the middle and upper troposphere (UT). We present a case study of convective transport during the GABRIEL campaign over the tropical rain forest in Suriname in October 2005. During one measurement flight the inflow and outflow regions of a cumulonimbus cloud (Cb) have been characterized. We identified a distinct layer between 9 and 11 km altitude with enhanced mixing ratios of CO, O3, HOx, acetone and acetonitrile. The elevated O3 contradicts the expectation that convective transport brings low-ozone air from the boundary layer to the outflow region. Entrainment of ozone-rich air is estimated to account for 62% (range: 33-91%) of the observed O3. Ozone is enhanced by only 5-6% by photochemical production in the outflow due to enhanced NO from lightning, based on model calculations using observations including the first reported HOx measurements over the tropical rainforest. The "excess" ozone in the outflow is most probably due to direct production by corona discharge associated with lightning. We deduce a production rate of 5.12 × 1028 molecules O3 flash-1 (range: 9.89 × 1026-9.82 × 1028 molecules O3 flash-1), which is at the upper limit of the range reported previously.

Development of hydroponic system using agricultural waste. 2. Utilization of ozone for sterilization of nutrient solution; Suiko saibai ni okeru haikibutsu riyo gijutsu no kaihatsu. 2. Ozone ni yoru baiyoeki sakkin ni kansuru kento

Energy Technology Data Exchange (ETDEWEB)

Terazoe, H; Yoshihara, T; Nakaya, K [Central Research Institute of Electric Power Industry, Tokyo (Japan)

1995-08-01

Discussions were given on a sterilizing effect of ozone on Fusarium bacteria in hydroponic culture, and its effect on components in the culture solution. In an experiment, dry air with O3 concentration of 3.5 ppm was sent into aqueous solution inoculated with Fusarium bacteria at a flow rate of 5 liters per minute. The Fusarium bacteria was sterilized nearly completely in about five minutes. No change was observed in pH, EC and dissolved oxygen concentration of the O3-treated culture solution. However, iron and manganese among the soluble components have been oxidized by O3 and precipitated, hence these components must be added after the O3 treatment. In spinach culture performed on a culture medium inoculated with Fusarium bacteria, ozone water containing dissolved O3 at 0.8 ppm was flown into a urethane foam medium and vegetable roots. This treatment has resulted in reduction of the number of strains occurred with a wilt symptom below that in the section flown with distilled water. The spinach has grown normally without showing an effect of the ozone water. 15 refs., 10 figs., 3 tabs.

Ozone treatment of textile wastewater relevant to toxic effect elimination in marine environment

OpenAIRE

Guendy, H.R.

2007-01-01

Ozone is a powerful oxidizing agent. The reaction of ozone with organic compounds in aqueous media has achieved a variety of treatment goals. The advantage of ozonation over the other oxidants is that the degradable products of ozonation are generally non-toxic, its final products are CO2 and H2O, and also the residual O3 in the system changes in few minutes to O2 .Convential treatment of textile wastewater includes various combinations of biological (activated sludge), physical and chemical ...

Spatial and temporal variation of surface ozone, NO and NO₂ at urban, suburban, rural and industrial sites in the southwest of the Iberian Peninsula.

Science.gov (United States)

Domínguez-López, D; Adame, J A; Hernández-Ceballos, M A; Vaca, F; De la Morena, B A; Bolívar, J P

2014-09-01

Surface ozone is one of the most important photochemical pollutants in the low atmosphere, causing damage to human health, vegetation, materials and climate. The weather (high temperatures and high solar radiation), orography (presence of the Guadalquivir valley) and anthropogenic (the cities of Cádiz, Córdoba, Huelva and Seville and two important industrial complexes) characteristics of the southwestern Iberian Peninsula make this region ideal for the formation and accumulation of ozone. To increase the knowledge of ozone behaviour in this area, the monthly, daily and weekly variations of ozone and its precursors, nitrogen oxides (NO(x) = NO + NO2), were analysed over a 4-year period (2003 to 2006). Using the k-means cluster technique, 12 representative stations of five different areas with different ozone behaviour were selected from a total of 29 monitoring sites. This is the first time that the analysis of these atmospheric pollutants has been carried out for the whole area, allowing therefore a complete understanding of the dynamics and the relationships of these compounds in this region. The results showed an opposite behaviour among ozone and NO and NO2 concentrations in urban and suburban zones, marked by maximums of ozone (minimums NO(x)) in spring and summer and minimums (maximums) in autumn and winter. A seasonal behaviour, with lower amplitude, was also observed in rural and industrial areas for ozone concentrations, with the NO and NO2 concentrations remaining at low and similar values during the year in rural zones due to the absence of emission sources in their surroundings. The daily cycles of ozone in urban, suburban and industrial sites registered a maximum value in the early afternoon (14:00-17:00 UTC) while for NOx two peaks were observed, at 7:00-10:00 UTC and 20:00-22:00. In the case of rural stations, no hourly peak of ozone or NO(x) was registered. The weekend effect was studied by using a statistical contrast tests (Student's t

Exposure-Relevant Ozone Chemistry in Occupied Spaces

Energy Technology Data Exchange (ETDEWEB)

Coleman, Beverly Kaye [Univ. of California, Berkeley, CA (United States)

2009-04-01

Ozone, an ambient pollutant, is transformed into other airborne pollutants in the indoor environment. In this dissertation, the type and amount of byproducts that result from ozone reactions with common indoor surfaces, surface residues, and vapors were determined, pollutant concentrations were related to occupant exposure, and frameworks were developed to predict byproduct concentrations under various indoor conditions. In Chapter 2, an analysis is presented of secondary organic aerosol formation from the reaction of ozone with gas-phase, terpene-containing consumer products in small chamber experiments under conditions relevant for residential and commercial buildings. The full particle size distribution was continuously monitored, and ultrafine and fine particle concentrations were in the range of 10 to>300 mu g m^-3. Particle nucleation and growth dynamics were characterized.Chapter 3 presents an investigation of ozone reactions with aircraft cabin surfaces including carpet, seat fabric, plastics, and laundered and worn clothing fabric. Small chamber experiments were used to determine ozone deposition velocities, ozone reaction probabilities, byproduct emission rates, and byproduct yields for each surface category. The most commonly detected byproducts included C1?C10 saturated aldehydes and skin oil oxidation products. For all materials, emission rates were higher with ozone than without. Experimental results were used to predict byproduct exposure in the cabin and compare to other environments. Byproduct levels are predicted to be similar to ozone levels in the cabin, which have been found to be tens to low hundreds of ppb in the absence of an ozone converter. In Chapter 4, a model is presented that predicts ozone uptake by and byproduct emission from residual chemicals on surfaces. The effects of input parameters (residue surface concentration, ozone concentration, reactivity of the residue and the surface, near-surface airflow conditions, and

tavgM_3d_odt_Cp: MERRA 3D IAU Tendency, Ozone, Monthly Mean 1.25 x 1.25 degree V5.2.0 (MATMCPODT) at GES DISC

Data.gov (United States)

National Aeronautics and Space Administration — The MATMCPODT or tavgM_3d_odt_Cp data product is the MERRA Data Assimilation System 3-Dimensional ozone tendencies that is time averaged on pressure levels at a...

Evaluating A Priori Ozone Profile Information Used in TEMPO Tropospheric Ozone Retrievals

Science.gov (United States)

Johnson, Matthew S.; Sullivan, John T.; Liu, Xiong; Newchurch, Mike; Kuang, Shi; McGee, Thomas J.; Langford, Andrew O'Neil; Senff, Christoph J.; Leblanc, Thierry; Berkoff, Timothy;

Evaluating A Priori Ozone Profile Information Used in TEMPO Tropospheric Ozone Retrievals

Science.gov (United States)

Johnson, M. S.; Sullivan, J. T.; Liu, X.; Newchurch, M.; Kuang, S.; McGee, T. J.; Langford, A. O.; Senff, C. J.; Leblanc, T.; Berkoff, T.; Gronoff, G.; Chen, G.; Strawbridge, K. B.

2016-12-01

Ozone (O3) is a greenhouse gas and toxic pollutant which plays a major role in air quality. Typically, monitoring of surface air quality and O3 mixing ratios is primarily conducted using in situ measurement networks. This is partially due to high-quality information related to air quality being limited from space-borne platforms due to coarse spatial resolution, limited temporal frequency, and minimal sensitivity to lower tropospheric and surface-level O3. The Tropospheric Emissions: Monitoring of Pollution (TEMPO) satellite is designed to address these limitations of current space-based platforms and to improve our ability to monitor North American air quality. TEMPO will provide hourly data of total column and vertical profiles of O3 with high spatial resolution to be used as a near-real-time air quality product. TEMPO O3 retrievals will apply the Smithsonian Astrophysical Observatory profile algorithm developed based on work from GOME, GOME-2, and OMI. This algorithm uses a priori O3 profile information from a climatological data-base developed from long-term ozone-sonde measurements (tropopause-based (TB) O3 climatology). It has been shown that satellite O3 retrievals are sensitive to a priori O3 profiles and covariance matrices. During this work we investigate the climatological data to be used in TEMPO algorithms (TB O3) and simulated data from the NASA GMAO Goddard Earth Observing System (GEOS-5) Forward Processing (FP) near-real-time (NRT) model products. These two data products will be evaluated with ground-based lidar data from the Tropospheric Ozone Lidar Network (TOLNet) at various locations of the US. This study evaluates the TB climatology, GEOS-5 climatology, and 3-hourly GEOS-5 data compared to lower tropospheric observations to demonstrate the accuracy of a priori information to potentially be used in TEMPO O3 algorithms. Here we present our initial analysis and the theoretical impact on TEMPO retrievals in the lower troposphere.

Inhibiting the regeneration of N-nitrosodimethylamine in drinking water by UV photolysis combined with ozonation

International Nuclear Information System (INIS)

Xu Bingbing; Chen Zhonglin; Qi Fei; Ma Jun; Wu Fengchang

2009-01-01

N-Nitrosodimethylamine (NDMA) is a highly carcinogenic compound that is suspected of carcinogenic activity in the human body. A variety of methods are used to remove NDMA from water, but the main degradation products, dimethylamine (DMA) and NO 2 - , are also precursors for NDMA formation. UV irradiation combined with ozonation (UV/O 3 ) was examined in this investigation for its ability to inhibit the regeneration of NDMA after degradation. Both the degradation products and the regeneration potential of NDMA were compared between UV irradiation alone and UV/O 3 . The yields of DMA and NO 2 - in the UV/O 3 process were less than for UV irradiation alone. Yields of DMA and NO 2 - were 2.25 mg L -1 and 3.22 mg L -1 from UV irradiation, while they were 0.92 mg L -1 and 0.45 mg L -1 from the UV/O 3 process. Furthermore, the regeneration of NDMA was also less after the UV/O 3 process than after UV irradiation. The concentration of regenerated NDMA was more than 51.8 μg L -1 after UV irradiation regardless of the dosage of Cl 2 . However, the concentration of regenerated NDMA in the UV/O 3 process was less than 7.37 μg L -1 under the same conditions. Consequently, the UV/O 3 process was more effective than UV irradiation alone in inhibiting NDMA regeneration. The inhibition of NDMA regeneration was due to a decrease in DMA and NO 2 - produced by the UV/O 3 process. As the major products generated from NDMA, NO 2 - and DMA were likely to be oxidized by ozone and hydroxyl radicals (·OH). In addition, the reaction between NDMA and ·OH would possibly generate methylamine as the only product, leading to a decrease in the production of DMA by the UV/O 3 process.

Tetracycline degradation by ozonation in the aqueous phase: Proposed degradation intermediates and pathway

International Nuclear Information System (INIS)

Khan, M. Hammad; Bae, Hyokwan; Jung, Jin-Young

2010-01-01

During the ozonation of tetracycline (TC) in aqueous media at pHs 2.2 and 7.0, the effects of pH variations, protonation and dissociation of functional groups and variation in free radical exposure were investigated to elucidate the transformation pathway. Liquid chromatography-triple quadrupole mass spectrometry detected around 15 ozonation products, and uncovered their production and subsequent degradation patterns. During ozonation at pH 2.2, the TC degradation pathway was proposed on the basis of the structure, ozonation chemistry and mass spectrometry data of TC. Ozonation of TC at the C11a-C12 and C2-C3 double bonds, aromatic ring and amino group generated products of m/z 461, 477, 509 and 416, respectively. Further ozonation at the above mentioned sites gave products of m/z 432, 480, 448, 525 and 496. The removal of TOC reached a maximum of ∼40% after 2 h of ozonation, while TC was completely removed within 4-6 min at both pHs. The low TOC removal efficiency might be due to the generation of recalcitrant products and the low ozone supply for high TC concentration. Ozonation decreased the acute toxicity of TC faster at pH 7.0 than pH 2.2, but the maximum decrease was only about 40% at both pHs after 2 h of ozonation. In this study, attempts were made to understand the correlation between the transformation products, pathway, acute toxicity and quantity of residual organics in solution. Overall, ozonation was found to be a promising process for removing TC and the products initially generated.

Effective cloud fractions from the Ozone Monitoring Instrument: theoretical framework and validation

NARCIS (Netherlands)

Stammes, P.; Sneep, M.; Haan, de J.F.; Veefkind, J.P.; Wang, P.; Levelt, P.F.

2008-01-01

The Dutch-Finnish Ozone Monitoring Instrument (OMI) on board NASA's EOS-Aura satellite is measuring ozone, NO2, and other trace gases with daily global coverage. To correct these trace gas retrievals for the presence of clouds, there are two OMI cloud products, based on different physical processes,

OMI/Aura Ozone (O3) DOAS Total Column Daily L2 Global 0.25 deg Lat/Lon Grid V003

Data.gov (United States)

National Aeronautics and Space Administration — The OMI/Aura Level-2G Total Column Ozone Data Product OMDOAO3G (Version 003) is now available ( http://disc.gsfc.nasa.gov/Aura/OMI/omdoao3g_v003.shtml ) from the...

Pollution Control Using Ozone

DEFF Research Database (Denmark)

2017-01-01

This invention relates to a method for cleaning air comprising one or more pollutants, the method comprising contacting the air with thermal decompositions products of ozone.......This invention relates to a method for cleaning air comprising one or more pollutants, the method comprising contacting the air with thermal decompositions products of ozone....

Stratospheric ozone chemistry in the Antarctic: what determines the lowest ozone values reached and their recovery?

Directory of Open Access Journals (Sweden)

J.-U. Grooß

2011-12-01

Full Text Available Balloon-borne observations of ozone from the South Pole Station have been reported to reach ozone mixing ratios below the detection limit of about 10 ppbv at the 70 hPa level by late September. After reaching a minimum, ozone mixing ratios increase to above 1 ppmv on the 70 hPa level by late December. While the basic mechanisms causing the ozone hole have been known for more than 20 yr, the detailed chemical processes determining how low the local concentration can fall, and how it recovers from the minimum have not been explored so far. Both of these aspects are investigated here by analysing results from the Chemical Lagrangian Model of the Stratosphere (CLaMS. As ozone falls below about 0.5 ppmv, a balance is maintained by gas phase production of both HCl and HOCl followed by heterogeneous reaction between these two compounds in these simulations. Thereafter, a very rapid, irreversible chlorine deactivation into HCl can occur, either when ozone drops to values low enough for gas phase HCl production to exceed chlorine activation processes or when temperatures increase above the polar stratospheric cloud (PSC threshold. As a consequence, the timing and mixing ratio of the minimum ozone depends sensitively on model parameters, including the ozone initialisation. The subsequent ozone increase between October and December is linked mainly to photochemical ozone production, caused by oxygen photolysis and by the oxidation of carbon monoxide and methane.

Ozone in the food industry: Principles of ozone treatment, mechanisms of action, and applications: An overview.

Science.gov (United States)

Brodowska, Agnieszka Joanna; Nowak, Agnieszka; Śmigielski, Krzysztof

2017-04-10

The food contamination issue requires continuous control of food at each step of the production process. High quality and safety of products are equally important factors in the food industry. They may be achieved with several, more or less technologically advanced methodologies. In this work, we review the role, contribution, importance, and impact of ozone as a decontaminating agent used to control and eliminate the presence of microorganisms in food products as well as to extend their shelf-life and remove undesirable odors. Several researchers have been focusing on the ozone's properties and applications, proving that ozone treatment technology can be applied to all types of foods, from fruits, vegetables, spices, meat, and seafood products to beverages. A compilation of those works, presented in this review, can be a useful tool for establishing appropriate ozone treatment conditions, and factors affecting the improved quality and safety of food products. A critical evaluation of the advantages and disadvantages of ozone in the context of its application in the food industry is presented as well.

OZONE PRODUCTION IN THE PHILADELPHIA URBAN AREA DURING NE-OPS 99

International Nuclear Information System (INIS)

KLEINMAN, L.I.; DAUM, P.H.; BRECHTEL, F.; LEE, Y.N.; NUNNERMACKER, L.J.; SPRINGSTON, S.R.; WEINSTEIN-LLOYD, J.

2001-01-01

As part of the 1999 NARSTO Northeast Oxidant and Particulate Study (NE-OPS) field campaign, the DOE G-1 aircraft sampled trace gases and aerosols in and around the Philadelphia metropolitan area. Twenty research flights were conducted between July 25 and August 11. The overall goals of these flights were to obtain a mechanistic understanding of O(sub 3) production; to characterize the spatial and temporal behavior of photo-oxidants and aerosols; and to study the evolution of aerosol size distributions, including the process of new particle formation. Within the NE-OPS program, other groups provided additional trace gas, aerosol, and meteorological observations using aircraft, balloon, remote sensing, and surface based instruments (Phillbrick et al., 2000). In this article we provide an overview of the G-1 observations related to O(sub 3) production, focusing on the vertical distribution of pollutants. Ozone production rates are calculated using a box model that is constrained by observed trace gas concentrations. Highest O(sub 3) concentrations were observed on July 31, which we present as a case study. On that day, O(sub 3) concentrations above the 1-hour 120 ppb standard were observed downwind of Philadelphia and also in the plume of a single industrial facility located on the Delaware River south of the city

Effect of ozonation on minocycline degradation and N-Nitrosodimethylamine formation.

Science.gov (United States)

Lv, Juan; Li, Yong M

2018-06-07

The objective of this study was to assess reactivity of Minocycline (MNC) towards ozone and determine the effects of ozone dose, pH value, and water matrix on MNC degradation as well as to characterize N-Nitrosodimethylamine (NDMA) formation from MNC ozonation. The MNC initial concentration of the solution was set in the range of 2-20 mg/L to investigate NDMA formation during MNC ozonation. Four ozone doses (22.5, 37.2, 58.0, and 74.4 mg/min) were tested to study the effect of ozone dose. For the evaluation of effects of pH value, pH was adjusted from 5 to 9 in the presence of phosphate buffer. MNC ozonation experiments were also conducted in natural water to assess the influence of water matirx. The influence of the typical component of natural water was also investigated with the addition of HA and NaHCO 3 solution. Results indicated that ozone was effective in MNC removal. Consequently, NDMA and dimethylamine (DMA) were generated from MNC oxidation. Increasing pH value enhanced MNC removal but led to greater NDMA generation. Water matrices, such as HCO 3 - and humic acid, affected MNC degradation. Conversely, more NDMA accumulated due to the inhibition of NDMA oxidation by oxidant consumption. Though ⋅OH can enhance MNC degradation, ozone molecules were heavily involved in NDMA production. Seven transformation products were identified. However, only DMA and the unidentified tertiary amine containing DMA group contributed to NDMA formation.

Influence of corona discharge on the ozone budget in the tropical free troposphere: a case study of deep convection during GABRIEL

Science.gov (United States)

Bozem, H.; Fischer, H.; Gurk, C.; Schiller, C. L.; Parchatka, U.; Koenigstedt, R.; Stickler, A.; Martinez, M.; Harder, H.; Kubistin, D.; Williams, J.; Eerdekens, G.; Lelieveld, J.

2014-02-01

Convective redistribution of ozone and its precursors between the boundary layer (BL) and the free troposphere (FT) influences photochemistry, in particular that of the middle and upper troposphere (UT). We present a case study of convective transport during the GABRIEL campaign over the tropical rain forest in Suriname in October 2005. During a measurement flight on 12 October the inflow and outflow regions of a cumulonimbus cloud (Cb) have been characterized, providing evidence of convective transport. We identified a distinct layer between 9 and 11 km altitude with enhanced mixing ratios of CO, O3, HOx, acetone and acetonitrile. The elevated O3 contradicts the expectation that convective transport brings low ozone air from the boundary layer to the outflow region. The enhanced mixing ratio of ozone in the outflow was mainly of dynamical origin. Entrainment of ozone rich air at the outflow level into the convective outflow accounts for 62% (range: 33-91%) of the observed O3. Ozone is enhanced by only 5-6% by photochemical production in the outflow due to enhanced NO from lightning, based on steady state model calculations, using in-situ observations including the first reported HOx measurements over the tropical rainforest. The "excess" ozone in the outflow is most probably due to direct production by corona discharge associated with lightning. We deduce a production rate of 5.12 × 1028 molecules O3 flash-1 (range: 9.89 × 1026-9.82 × 1028 molecules O3 flash-1), which is at the upper limit of the range of the values reported previously.

Impact of the new HNO3-forming channel of the HO2+NO reaction on tropospheric HNO3, NOx, HOx and ozone

Directory of Open Access Journals (Sweden)

A. Kukui

2008-07-01

Full Text Available We have studied the impact of the recently observed reaction NO+HO2→HNO3 on atmospheric chemistry. A pressure and temperature-dependent parameterisation of this minor channel of the NO+HO2→NO2+OH reaction has been included in both a 2-D stratosphere-troposphere model and a 3-D tropospheric chemical transport model (CTM. Significant effects on the nitrogen species and hydroxyl radical concentrations are found throughout the troposphere, with the largest percentage changes occurring in the tropical upper troposphere (UT. Including the reaction leads to a reduction in NOx everywhere in the troposphere, with the largest decrease of 25% in the tropical and Southern Hemisphere UT. The tropical UT also has a corresponding large increase in HNO3 of 25%. OH decreases throughout the troposphere with the largest reduction of over 20% in the tropical UT. The mean global decrease in OH is around 13%, which is very large compared to the impact that typical photochemical revisions have on this modelled quantity. This OH decrease leads to an increase in CH4 lifetime of 5%. Due to the impact of decreased NOx on the OH:HO2 partitioning, modelled HO2 actually increases in the tropical UT on including the new reaction. The impact on tropospheric ozone is a decrease in the range 5 to 12%, with the largest impact in the tropics and Southern Hemisphere. Comparison with observations shows that in the region of largest changes, i.e. the tropical UT, the inclusion of the new reaction tends to degrade the model agreement. Elsewhere the model comparisons are not able to critically assess the impact of including this reaction. Only small changes are calculated in the minor species distributions in the stratosphere.

Tropospheric ozone trend over Beijing from 2002–2010: ozonesonde measurements and modeling analysis

Directory of Open Access Journals (Sweden)

Y. Wang

2012-09-01

Full Text Available Using a combination of ozonesonde data and numerical simulations of the Chemical Lagrangian Model of the Stratosphere (CLaMS, the trend of tropospheric ozone (O₃ during 2002–2010 over Beijing was investigated. Tropospheric ozone over Beijing shows a winter minimum and a broad summer maximum with a clear positive trend in the maximum summer ozone concentration over the last decade. The observed significant trend of tropospheric column ozone is mainly caused by photochemical production (3.1% yr⁻¹ for a mean level of 52 DU. This trend is close to the significant trend of partial column ozone in the lower troposphere (0–3 km resulting from the enhanced photochemical production during summer (3.0% yr⁻¹ for a mean level of 23 DU. Analysis of the CLaMS simulation shows that transport rather than chemistry drives most of the seasonality of tropospheric ozone. However, dynamical processes alone cannot explain the trend of tropospheric ozone in the observational data. Clearly enhanced ozone values and a negative vertical ozone gradient in the lower troposphere in the observational data emphasize the importance of photochemistry within the troposphere during spring and summer, and suggest that the photochemistry within the troposphere significantly contributes to the tropospheric ozone trend over Beijing during the last decade.

Characterization of N-nitrosodimethylamine formation from the ozonation of ranitidine.

Science.gov (United States)

Lv, Juan; Wang, Lin; Li, Yongmei

2017-08-01

N-nitrosodimethylamine (NDMA) is an emerging disinfection by-product which is formed during water disinfection in the presence of amine-based precursors. Ranitidine, as one kind of amine-based pharmaceuticals, has been identified as NDMA precursor with high NDMA molar conversion during chloramination. This study focused on the characterization of NDMA formation during ozonation of ranitidine. Influences of operational variables (ozone dose, pH value) and water matrix on NDMA generation as well as ranitidine degradation were evaluated. The results indicate high reactivity of ranitidine with ozone. Dimethylamine (DMA) and NDMA were generated due to ranitidine oxidation. High pH value caused more NDMA accumulation. NDMA formation was inhibited under acid conditions (pH≤5) mainly due to the protonation of amines. Water matrix such as HCO 3 - and humic acid impacted NDMA generation due to OH scavenging. Compared with OH, ozone molecules dominated the productions of DMA and NDMA. However, OH was a critical factor in NDMA degradation. Transformation products of ranitidine during ozonation were identified using gas chromatography-mass spectrometry. Among these products, just DMA and N,N-dimethylformamide could contribute to NDMA formation due to the DMA group in the molecular structures. The NDMA formation pathway from ranitidine ozonation was also proposed. Copyright © 2017. Published by Elsevier B.V.

The effects of ozone and NO{sub x} on the deterioration of calcareous stone

Energy Technology Data Exchange (ETDEWEB)

Massey, S.W. [Building Research Establishment Ltd, Garston, Watford (United Kingdom)

1999-03-09

This paper looks at the changes in urban air quality and the effect on building materials with particular regard to their deterioration arising from pollution due to vehicles. The paper aims to review basic information on the likely effect of NO{sub x} and ozone on calcareous building materials (limestone, marble, dolomite, calcareous cemented sandstone) by examining experimental and fieldwork relating to the principle reaction of the oxidation of the sulphite to sulphate. NO{sub 2} is only one of many possible oxidants present in the urban and rural environment. A brief synopsis of the effects of other oxidants and inhibitors is given along with a review of the processes involved in aqueous phase oxidation, which seems to be the phase where the reactions take place. Controlling factors in the reaction and oxidation of sulphite to sulphate are the type and porosity of the stone, the level of humidity, the nature of the oxidants and to a lesser extent the presence of other extraneous reactants, e.g. metal oxides, chlorine and ammonia salts. For freshly cut stone unpolished marble is much less reactive than porous limestone and the degree of activity has different relative humidity thresholds. Reaction of the stone with the gaseous compounds occurs during the process of absorption onto the surface. The oxidation is accelerated at the gas-water interface by the presence of NO{sub x}, and seems to depend on the NO{sub 2} component but it is clear that NO{sub x} is only one of many possible oxidants in the urban and rural environments. Correlation studies of the damage to stone materials are unlikely to pick up the effects of NO{sub x} due to the nature of their duration and the rather transient nature of the appearance and removal of nitrates on the stone. Presence of other oxidants and catalysts such as H{sub 2}O{sub 2}, O{sub 2} (catalysed by Fe{sup 3+} and Mn{sup 2+}), OH, HSO{sub 5}{sup -}, SO{sub 4}{sup 2-}, O{sub 3}, HO{sub 2}, NO{sub 2}{sup -}, NO{sub 3}, O

The effects of ozone and NO{sub x} on the deterioration of calcareous stone

Energy Technology Data Exchange (ETDEWEB)

Massey, S.W. [Building Research Establishment Ltd., Garston, Watford (United Kingdom)

1999-03-09

This paper looks at the changes in urban air quality and the effect on building materials with particular regard to their deterioration arising from pollution due to vehicles. The paper aims to review basic information on the likely effect of NO{sub x} and ozone on calcareous building materials (limestone, marble, dolomite, calcareous cemented sandstone) by examining experimental and fieldwork relating to the principle reaction of the oxidation of the sulphite to sulphate. NO{sub 2} is only one of many possible oxidants present in the urban and rural environment. A brief synopsis of the effects of other oxidants and inhibitors is given along with a review of the processes involved in aqueous phase oxidation, which seems to be the phase where the reactions take place. Controlling factors in the reaction and oxidation of sulphite to sulphate are the type and porosity of the stone, the level of humidity, the nature of the oxidants and to a lesser extent the presence of other extraneous reactants, e.g. metal oxides, chlorine and ammonia salts. For freshly cut stone unpolished marble is much less reactive than porous limestone and the degree of activity has different relative humidity thresholds. Reaction of the stone with the gaseous compounds occurs during the process of absorption onto the surface. The oxidation is accelerated at the gas-water interface by the presence of NO{sub x}, and seems to depend on the NO{sub 2} component but it is clear that NO{sub x} is only one of many possible oxidants in the urban and rural environments. Correlation studies of the damage to stone materials are unlikely to pick up the effects of NO{sub x} due to the nature of their duration and the rather transient nature of the appearance and removal of nitrates on the stone. Presence of other oxidants and catalysts such as H{sub 2}O{sub 2}, O{sub 2} (catalysed by Fe{sup 3+} and Mn{sup 2+}), OH, HSO{sub 5}{sup -}, SO{sub 4}{sup 2-}, O{sub 3}, HO{sub 2}, NO{sub 2}{sup -}, NO{sub 3}, O

An assessment of ozone levels, UV radiation and their occupational health hazard estimation during photocopying operation

Energy Technology Data Exchange (ETDEWEB)

Singh, Bhupendra Pratap, E-mail: bpsingh0783@gmail.com; Kumar, Amit; Singh, Deepak; Punia, Monika; Kumar, Krishan; Jain, Vinod Kumar

2014-06-30

Highlights: • First quantitative report of ozone level and UV radiation emission from photocopier. • Ozone production is directly proportional with intensity of photocopy operation. • Ozone level from ground floor is significantly higher than basement photocopier. • Ozone production and UV radiation studied has less correlation during photocopy. • Health hazard issue has been evaluated for effect of UV radiation in terms of SED. - Abstract: This study investigates the levels of ozone concentration along with an ultraviolet (UV) and visible spectral radiation at eight photocopy centers in an academic institute, Delhi. Sampling was done in two types of locations, i.e., basement photocopy centers (BPC) and ground floor photocopy centers (GPC) for 8 h. Measurements of levels of ozone, UV and visible radiation were done by ozone analyzer, UV radiometer and Field spectra instrument, respectively. Results show that the hourly mean concentration of ozone was observed to be in the range of 1.8–10.0 ppb and 5.3–45.8 ppb for BPC and GPC, respectively. In terms UV radiations, energy lies between 5.0 × 10{sup −3} and 7.0 × 10{sup −3} mW/cm{sup 2} for ultraviolet A (UVA), 1.0 × 10{sup −3} and 2.0 × 10{sup −3} mW/cm{sup 2} for ultraviolet B (UVB) and 6.0 × 10{sup −3} and 8.0 × 10{sup −3} mW/cm{sup 2} for ultraviolet C (UVC). Correlation between the UV radiations and ozone production observed was statistically insignificant. To know the health hazard occurred to the workers, the standard erythema dose (SED) value was calculated for emitting UV radiation. The SED was estimated to be in the range of 0.02–0.04 and 0.02–0.32 for direct and indirect methods which is less than the guideline prescribed by Commission Internationale del’ Eclairage (CIE). In nutshell, person involved in photocopy operation for their livelihood must be trained and should have knowledge for the long term gradual build up health problems due to ozone and UV production from

OMI/Aura TOMS-Like Ozone and Radiative Cloud Fraction Daily L3 Global 0.25x0.25 deg V003

Data.gov (United States)

National Aeronautics and Space Administration — The Version-003 of Level-3 Aura/OMI daily global TOMS-Like Total Column Ozone gridded product (OMTO3e) is generated by the NASA OMI science team by picking the best...

Impact of dedicated E85 vehicle use on ozone and particulate matter in the US

Science.gov (United States)

Nopmongcol, Uarporn; Griffin, W. Michael; Yarwood, Greg; Dunker, Alan M.; MacLean, Heather L.; Mansell, Gerard; Grant, John

2011-12-01

Increased use of ethanol as a vehicle fuel worldwide warrants the need to understand air quality impacts of replacing gasoline with ethanol. This study evaluates the impacts of dedicated E85 (85% ethanol/15% gasoline) light-duty vehicles on emissions, ozone and particulate matter (PM) concentrations in the United States for a future year (2022) using a 3-D photochemical model, detailed emissions inventories that account for changes in all sectors studied, and winter and summer meteorology that occurred in 2002. Use of E85 introduces new emissions from ethanol production and distribution, reduces petrochemical industry emissions due to lower gasoline consumption, changes on-road vehicle emissions and alters biogenic emissions due to land use changes. Three scenarios with increased ethanol production for dedicated E85 light-duty vehicles were compared to a base case without increased ethanol production. Increased use of E85 caused both increases and decreases in ozone and PM, driven mainly by changes in NO x emissions related to biogenic and upstream petrochemical industry sources. In all states modeled, adoption of dedicated E85 vehicles caused negligible change in average higher ozone and PM concentrations of importance for air quality management strategies. Ozone and PM changes are relatively insensitive to how land area is allocated for switchgrass production. The findings are subject to various uncertainties, especially those in vehicle technology and emissions from cellulosic ethanol production.

Sensitivity of the OMI ozone profile retrieval (OMO3PR) to a priori assumptions

NARCIS (Netherlands)

Mielonen, T.; De Haan, J.F.; Veefkind, J.P.

2014-01-01

We have assessed the sensitivity of the operational OMI ozone profile retrieval (OMO3PR) algorithm to a number of a priori assumptions. We studied the effect of stray light correction, surface albedo assumptions and a priori ozone profiles on the retrieved ozone profile. Then, we studied how to

Airborne measurements of NO{sub y} and impact of this trace gas on atmospheric chemistry

Energy Technology Data Exchange (ETDEWEB)

Perros, P E; Marion, T [Paris-12 et 7 Univ., Laboratoire Interuniversitaire des Systemes Atmospheriques, 94 - Creteil (France)

1999-05-01

Nitrogen compounds play a key role in the ozone production processes. The airborne measurement of individual species is difficult compared to their global measurement. This can be done by the conversion of all the species (NO{sub y}) in NO followed by a subsequent analysis by chemiluminescence. Laboratory tests allow up to determine the main characteristics of such conversion. NO{sub y} measurements associated with NO{sub x} concentrations allow a quantitative and qualitative study of ozone production processes. In particular it is possible to determine the ozone production potential of an air mass, the ozone production efficiency and to specify the chemical regimes. (authors) 13 refs.

Assessing ozone and nitrogen impact on net primary productivity with a Generalised non-Linear Model

International Nuclear Information System (INIS)

De Marco, Alessandra; Screpanti, Augusto; Attorre, Fabio; Proietti, Chiara; Vitale, Marcello

2013-01-01

Some studies suggest that in Europe the majority of forest growth increment can be accounted for N deposition and very little by elevated CO 2 . High ozone (O 3 ) concentrations cause reductions in carbon fixation in native plants by offsetting the effects of elevated CO 2 or N deposition. The cause-effect relationships between primary productivity (NPP) of Quercus cerris, Q. ilex and Fagus sylvatica plant species and climate and pollutants (O 3 and N deposition) in Italy have been investigated by application of Generalised Linear/non-Linear regression model (GLZ model). The GLZ model highlighted: i) cumulative O 3 concentration-based indicator (AOT40F) did not significantly affect NPP; ii) a differential action of oxidised and reduced nitrogen depositions to NPP was linked to the geographical location; iii) the species-specific variation of NPP caused by combination of pollutants and climatic variables could be a potentially important drive-factor for the plant species' shift as response to the future climate change. - Highlights: ► GLZ Models emphasized the role of combination of variables affecting NPP. ► A differential action of ox-N and red-N deposition to NPP was observed for plants. ► Different responses to climate and pollutants could affect the plant species' shift. - Ozone and nitrogen depositions have non-linear effects on primary productivity of tree species differently distributed in Italy.

Latitudinal distribution of total ozone and NO[sub 2] over the Atlantic Ocean according to measurements in May 1988

Energy Technology Data Exchange (ETDEWEB)

Elokhov, A.S; Gruzdev, A.N. (Inst. Fiziki Atmosfery, Moscow (Russian Federation))

1992-07-01

Measurements of the total ozone and NO[sub 2] content conducted on board a ship in the 40 deg S - 40 deg N latitudinal belt in the Atlantic Ocean in the second half of May 1988 are reported. The main features of the latitudinal distributions of total ozone and NO[sub 2] are similar. Both distributions have minima in the equatorial zone of the Southern Hemisphere, and both the ozone and NO[sub 2] contents increase from tropical to subtropical latitudes. This increase is the strongest in the subtropical jet stream zone. The fine structure of the studied distributions is also revealed, and its relationship to stratosphere-troposphere exchange processes in the tropopause folding region is discussed. The evening total NO[sub 2] content systematically exceeds that of the morning due to diurnal variations. 20 refs.

The impact of biogenic VOC emissions on photochemical ozone formation during a high ozone pollution episode in the Iberian Peninsula in the 2003 summer season

Directory of Open Access Journals (Sweden)

N. Castell

2008-04-01

Full Text Available Throughout Europe the summer of 2003 was exceptionally warm, especially July and August. The European Environment Agency (EEA reported several ozone episodes, mainly in the first half of August. These episodes were exceptionally long-lasting, spatially extensive, and associated to high temperatures. In this paper, the 10$ndash;15 August 2003 ozone pollution event has been analyzed using meteorological and regional air quality modelling. During this period the threshold values of the European Directive 2002/3/EC were exceeded in various areas of the Iberian Peninsula.

The aim of this paper is to computationally understand and quantify the influence of biogenic volatile organic compound (BVOC emissions in the formation of tropospheric ozone during this high ozone episode. Being able to differentiate how much ozone comes from biogenic emissions alone and how much comes from the interaction between anthropogenic and biogenic emissions would be helpful to develop a feasible and effective ozone control strategy. The impact on ozone formation was also studied in combination with various anthropogenic emission reduction strategies, i.e., when anthropogenic VOC emissions and/or NO_x emissions are reduced. The results show a great dependency of the BVOC contribution to ozone formation on the antropoghenic reduction scenario. In rural areas, the impact due to a NO_x and/or VOC reduction does not change the BVOC impact. Nevertheless, within big cities or industrial zones, a NO_x reduction results in a decrease of the biogenic impact in ozone levels that can reach 85 μg/m³, whereas an Anthropogenic Volatile Organic Compound (AVOC reduction results in a decrease of the BVOC contribution on ozone formation that varies from 0 to 30 μg/m³ with respect to the contribution at the same points in the 2003 base scenario. On the other hand, downwind of the big cities, a decrease in NO_x produces

Effects of ozone-vegetation coupling on surface ozone air quality via biogeochemical and meteorological feedbacks

Science.gov (United States)

Sadiq, Mehliyar; Tai, Amos P. K.; Lombardozzi, Danica; Martin, Maria Val

2017-02-01

Tropospheric ozone is one of the most hazardous air pollutants as it harms both human health and plant productivity. Foliage uptake of ozone via dry deposition damages photosynthesis and causes stomatal closure. These foliage changes could lead to a cascade of biogeochemical and biogeophysical effects that not only modulate the carbon cycle, regional hydrometeorology and climate, but also cause feedbacks onto surface ozone concentration itself. In this study, we implement a semi-empirical parameterization of ozone damage on vegetation in the Community Earth System Model to enable online ozone-vegetation coupling, so that for the first time ecosystem structure and ozone concentration can coevolve in fully coupled land-atmosphere simulations. With ozone-vegetation coupling, present-day surface ozone is simulated to be higher by up to 4-6 ppbv over Europe, North America and China. Reduced dry deposition velocity following ozone damage contributes to ˜ 40-100 % of those increases, constituting a significant positive biogeochemical feedback on ozone air quality. Enhanced biogenic isoprene emission is found to contribute to most of the remaining increases, and is driven mainly by higher vegetation temperature that results from lower transpiration rate. This isoprene-driven pathway represents an indirect, positive meteorological feedback. The reduction in both dry deposition and transpiration is mostly associated with reduced stomatal conductance following ozone damage, whereas the modification of photosynthesis and further changes in ecosystem productivity are found to play a smaller role in contributing to the ozone-vegetation feedbacks. Our results highlight the need to consider two-way ozone-vegetation coupling in Earth system models to derive a more complete understanding and yield more reliable future predictions of ozone air quality.

Approach for detecting mutagenicity of biodegraded and ozonated pharmaceuticals, metabolites and transformation products from a drinking water perspective.

Science.gov (United States)

Gartiser, Stefan; Hafner, Christoph; Kronenberger-Schäfer, Kerstin; Happel, Oliver; Trautwein, Christoph; Kümmerer, Klaus

2012-09-01

Many pharmaceuticals and related metabolites are not efficiently removed in sewage treatment plants and enter into surface water. There, they might be subject of drinking water abstraction and treatment by ozonation. In this study, a systematic approach for producing and effect-based testing of transformation products (TPs) during the drinking water ozonation process is proposed. For this, two pharmaceutical parent substances, three metabolites and one environmental degradation product were investigated with respect to their biodegradability and fate during drinking water ozonation. The Ames test (TA98, TA100) was used for the identification of mutagenic activity present in the solutions after testing inherent biodegradability and/or after ozonation of the samples. Suspicious results were complemented with the umu test. Due to the low substrate concentration required for ozonation, all ozonated samples were concentrated via solid phase extraction (SPE) before performing the Ames test. With the exception of piracetam, all substances were only incompletely biodegradable, suggesting the formation of stable TPs. Metformin, piracetam and guanylurea could not be removed completely by the ozonation process. We received some evidence that technical TPs are formed by ozonation of metformin and piracetam, whereas all tested metabolites were not detectable by analytical means after ozonation. In the case of guanylurea, one ozonation TP was identified by LC/MS. None of the experiments showed an increase of mutagenic effects in the Ames test. However, the SPE concentration procedure might lead to false-positive results due to the generation of mutagenic artefacts or might lead to false-negative results by missing adequate recovery efficiency. Thus, these investigations should always be accompanied by process blank controls that are carried out along the whole ozonation and SPE procedure. The study presented here is a first attempt to investigate the significance of

The Tropospheric Ozone Assessment Report (TOAR): A community-wide effort to quantify tropospheric ozone in a rapidly changing world

Science.gov (United States)

Cooper, O. R.; Schultz, M.; Paoletti, E.; Galbally, I. E.; Naja, M. K.; Tarasick, D. W.; Evans, M. J.; Thompson, A. M.

2017-12-01

Tropospheric ozone is a greenhouse gas and pollutant detrimental to human health and crop and ecosystem productivity. Since 1990 a large portion of the anthropogenic emissions that react in the atmosphere to produce ozone has shifted from North America and Europe to Asia. This rapid shift, coupled with limited ozone monitoring in developing nations, left scientists unable to answer the most basic questions: Which regions of the world have the greatest human and plant exposure to ozone pollution? Is ozone continuing to decline in nations with strong emissions controls? To what extent is ozone increasing in the developing world? How can the atmospheric sciences community facilitate access to the ozone metrics necessary for quantifying ozone's impact on human health and crop/ecosystem productivity? To answer these questions the International Global Atmospheric Chemistry Project (IGAC) initiated the Tropospheric Ozone Assessment Report (TOAR). With over 220 member scientists and air quality specialists from 36 nations, TOAR's mission is to provide the research community with an up-to-date scientific assessment of tropospheric ozone's global distribution and trends from the surface to the tropopause. TOAR has also built the world's largest database of surface ozone observations and generated ozone exposure and dose metrics at thousands of measurement sites around the world, freely accessible for research on the global-scale impact of ozone on climate, human health and crop/ecosystem productivity. Plots of these metrics show the regions of the world with the greatest ozone exposure for humans and crops/ecosystems, at least in areas where observations are available. The results also highlight regions where air quality is improving and where it has degraded. TOAR has also conducted the first intercomparison of tropospheric column ozone from ozonesondes and multiple satellite instruments, which provide similar estimates of the present-day tropospheric ozone burden.

Identification of intermediates and assessment of ecotoxicity in the oxidation products generated during the ozonation of clofibric acid.

Science.gov (United States)

Rosal, Roberto; Gonzalo, María S; Boltes, Karina; Letón, Pedro; Vaquero, Juan J; García-Calvo, E

2009-12-30

The degradation of an aqueous solution of clofibric acid was investigated during catalytic and non-catalytic ozonation. The catalyst, TiO(2), enhanced the production of hydroxyl radicals from ozone and raised the fraction or clofibric acid degraded by hydroxyl radicals. The rate constant for the reaction of clofibric acid and hydroxyl radicals was not affected by the presence of the catalyst. The toxicity of the oxidation products obtained during the reaction was assessed by means of Vibrio fischeri and Daphnia magna tests in order to evaluate the potential formation of toxic by-products. The results showed that the ozonation was enhanced by the presence of TiO(2,) the clofibric acid being removed completely after 15 min at pH 5. The evolution of dissolved organic carbon, specific ultraviolet absorption at 254 nm and the concentration of carboxylic acids monitored the degradation process. The formation of 4-chlorophenol, hydroquinone, 4-chlorocatechol, 2-hydroxyisobutyric acid and three non-aromatic compounds identified as a product of the ring-opening reaction was assessed by exact mass measurements performed by liquid chromatography coupled to time-of-flight mass spectrometry (LC-TOF-MS). The bioassays showed a significant increase in toxicity during the initial stages of ozonation following a toxicity pattern closely related to the formation of ring-opening by-products.

Effect of ozone concentration on silicon surface passivation by atomic layer deposited Al2O3

International Nuclear Information System (INIS)

Gastrow, Guillaume von; Li, Shuo; Putkonen, Matti; Laitinen, Mikko; Sajavaara, Timo; Savin, Hele

2015-01-01

Highlights: • The ALD Al 2 O 3 passivation quality can be controlled by the ozone concentration. • Ozone concentration affects the Si/Al 2 O 3 interface charge and defect density. • A surface recombination velocity of 7 cm/s is reached combining ozone and water ALD. • Carbon and hydrogen concentrations correlate with the surface passivation quality. - Abstract: We study the impact of ozone-based Al 2 O 3 Atomic Layer Deposition (ALD) on the surface passivation quality of crystalline silicon. We show that the passivation quality strongly depends on the ozone concentration: the higher ozone concentration results in lower interface defect density and thereby improved passivation. In contrast to previous studies, our results reveal that too high interface hydrogen content can be detrimental to the passivation. The interface hydrogen concentration can be optimized by the ozone-based process; however, the use of pure ozone increases the harmful carbon concentration in the film. Here we demonstrate that low carbon and optimal hydrogen concentration can be achieved by a single process combining the water- and ozone-based reactions. This process results in an interface defect density of 2 × 10 11 eV −1 cm −2 , and maximum surface recombination velocities of 7.1 cm/s and 10 cm/s, after annealing and after an additional firing at 800 °C, respectively. In addition, our results suggest that the effective oxide charge density can be optimized in a simple way by varying the ozone concentration and by injecting water to the ozone process.

Ozone decreases soybean productivity and water use efficiency

Science.gov (United States)

Betzelberger, A. M.; VanLoocke, A. D.; Ainsworth, E. A.; Bernacchi, C. J.

2011-12-01

The combination of population growth and climate change will increase pressure on agricultural and water resources throughout this century. An additional consequence of this growth is an increase in anthropogenic emissions that lead to the formation of tropospheric ozone (O3), which in concert with climate change, poses a significant threat to human health and nutrition. In addition to being an important greenhouse gas, O3 reduces plant productivity, an effect that has been particularly pronounced in soybean, which provides over half of the world's oilseed production. Plant productivity is linked to feedbacks in the climate system, indirectly through the carbon cycle, as well as directly through the partitioning of radiation into heat and moisture fluxes. Soybean, along with maize, comprises the largest ecosystem in the contiguous U.S. Therefore, changes in productivity and water use under increasing O3 could impact human nutrition as well as the regional climate. Soybean response to increasing O3 concentrations was tested under open-air agricultural conditions at the SoyFACE research site. During the 2009 growing season, eight 20 m diameter FACE plots were exposed to different O3 concentrations, ranging from 40 to 200 ppb. Canopy growth (leaf area index) and physiological measurements of leaf photosynthesis and stomatal conductance were taken regularly throughout the growing season. Canopy fluxes of heat and moisture were measured using the residual energy balance micrometeorological technique. Our results indicate that as O3 increased from 40 to 200 ppb, rates of photosynthesis and stomatal conductance decreased significantly. Further, the seed yield decreased by over 60%, while water use decreased by 30% and the water-use-efficiency (yield/water-use) declined by 50%. The growing season average canopy temperatures increased by 1°C and midday temperatures increased by 2°C compared to the control. Warmer and drier canopies may result in a positive feedback on O3

A statistical model to predict total column ozone in Peninsular Malaysia

Science.gov (United States)

Tan, K. C.; Lim, H. S.; Mat Jafri, M. Z.

2016-03-01

This study aims to predict monthly columnar ozone in Peninsular Malaysia based on concentrations of several atmospheric gases. Data pertaining to five atmospheric gases (CO2, O3, CH4, NO2, and H2O vapor) were retrieved by satellite scanning imaging absorption spectrometry for atmospheric chartography from 2003 to 2008 and used to develop a model to predict columnar ozone in Peninsular Malaysia. Analyses of the northeast monsoon (NEM) and the southwest monsoon (SWM) seasons were conducted separately. Based on the Pearson correlation matrices, columnar ozone was negatively correlated with H2O vapor but positively correlated with CO2 and NO2 during both the NEM and SWM seasons from 2003 to 2008. This result was expected because NO2 is a precursor of ozone. Therefore, an increase in columnar ozone concentration is associated with an increase in NO2 but a decrease in H2O vapor. In the NEM season, columnar ozone was negatively correlated with H2O (-0.847), NO2 (0.754), and CO2 (0.477); columnar ozone was also negatively but weakly correlated with CH4 (-0.035). In the SWM season, columnar ozone was highly positively correlated with NO2 (0.855), CO2 (0.572), and CH4 (0.321) and also highly negatively correlated with H2O (-0.832). Both multiple regression and principal component analyses were used to predict the columnar ozone value in Peninsular Malaysia. We obtained the best-fitting regression equations for the columnar ozone data using four independent variables. Our results show approximately the same R value (≈ 0.83) for both the NEM and SWM seasons.

Heterogeneous reactions of ozone with methoxyphenols, in presence and absence of light

Science.gov (United States)

Net, Sopheak; Alvarez, Elena Gómez; Gligorovski, Sasho; Wortham, Henri

2011-06-01

In this work, we investigated the heterogeneous reactions between gaseous ozone and seven particulate methoxyphenols, biomass tracers. The ozonolysis of silica particles coated with vanillin, vanillic acid, syringaldehyde, syringic acid, acetovanillone, acetonsyringone and coniferyl alcohol was studied successively and was carried out both in total darkness and under illumination with simulated solar light at 297 K. The condensed-phase products which emerged in such heterogeneous reactions were analyzed by gas chromatography-mass spectrometry (GC/MS). No reaction product was detected during the ozonolysis of vanillic acid, syringic acid, acetovanillone and acetosyringone under our experimental conditions. The main tranformation of pathway vanillin and syringaldehyde was the conversion of an aldehyde group to a carboxylic fonction. Thus, syringic acid and vanillic acid were respectively the main oxidation products of syringaldehyde and vanillin. The oxidation of coniferyl alcohol was relatively fast and the total degradation was observed after 16 h of ozone exposure. Five oxidation products: glycolic acid, oxalic acid, vanillin, vanillic acid and 3,4-dihydroxybenzoic acid, were identified and confirmed by their corresponding standards. It is interesting to note that 3,4-dihydroxybenzoic acid was detected only in the experiment performed under combined ozone and light exposure of the particles coated with coniferyl alcohol. Vanillin and vanillic acid also absorb light in the tropospheric actinic window and therefore they can be photochemically active which in turn can induce further modifications of the aerosol particles. A mechanistic pathway was proposed in order to elucidate the ozonolysis reaction of coniferyl alcohol and to explain the identified reaction products.

TOMS/Earth Probe Total Column Ozone Daily L3 Global 1x1.25 deg Lat/Lon Grid V008

Data.gov (United States)

National Aeronautics and Space Administration — This data product contains TOMS/Earth Probe Total Column Ozone Daily L3 Global 1x1.25 deg Lat/Lon Grid Version 8 data in ASCII format. (The shortname for this...

"OZONE SOURCE APPORTIONMENT IN CMAQ' | Science ...

Science.gov (United States)

Ozone source attribution has been used to support various policy purposes including interstate transport (Cross State Air Pollution Rule) by U.S. EPA and ozone nonattainment area designations by State agencies. Common scientific applications include tracking intercontinental transport of ozone and ozone precursors and delineating anthropogenic and non-anthropogenic contribution to ozone in North America. As in the public release due in September 2013, CMAQ’s Integrated Source Apportionment Method (ISAM) attributes PM EC/OC, sulfate, nitrate, ammonium, ozone and its precursors NOx and VOC, to sectors/regions of users’ interest. Although the peroxide-to-nitric acid productions ratio has been the most common indicator to distinguish NOx-limited ozone production from VOC-limited one, other indicators are implemented in addition to allowing for an ensemble decision based on a total of 9 available indicator ratios. Moreover, an alternative approach of ozone attribution based on the idea of chemical sensitivity in a linearized system that has formed the basis of chemical treatment in forward DDM/backward adjoint tools has been implemented in CMAQ. This method does not require categorization into either ozone regime. In this study, ISAM will simulate the 2010 North America ozone using all of the above gas-phase attribution methods. The results are to be compared with zero-out difference out of those sectors in the host model runs. In addition, ozone contribution wil

Meteorological and chemical impacts on ozone formation: A case study in Hangzhou, China

Science.gov (United States)

Li, Kangwei; Chen, Linghong; Ying, Fang; White, Stephen J.; Jang, Carey; Wu, Xuecheng; Gao, Xiang; Hong, Shengmao; Shen, Jiandong; Azzi, Merched; Cen, Kefa

2017-11-01

Regional ozone pollution has become one of the most challenging problems in China, especially in the more economically developed and densely populated regions like Hangzhou. In this study, measurements of O3, CO, NOx and non-methane hydrocarbons (NMHCs), together with meteorological data, were obtained for the period July 1, 2013-August 15, 2013 at three sites in Hangzhou. These sites included an urban site (Zhaohui ;ZH;), a suburban site (Xiasha ;XS;) and a rural site (Qiandaohu ;QDH;). During the observation period, both ZH and XS had a higher ozone level than QDH, with exceeding rates of 41.3% and 47.8%, respectively. Elevated O3 levels in QDH were found at night, which could be explained by less prominent NO titration effect in rural area. Detailed statistical analysis of meteorological and chemical impacts on ozone formation was carried out for ZH, and higher ozone concentration was observed when the wind direction was from the east. This is possibly due to emissions of VOCs from XS, a typical chemical industrial park located in 30 km upwind area of ZH. A comprehensive comparison between three ozone episode periods and one non-episode period were made in ZH. It was concluded that elevated concentrations of precursors and temperatures, low relative humidity and wind speed and easterly-dominated wind direction contribute to urban ozone episodes in Hangzhou. VOCs reactivity analysis indicated that reactive alkenes like isoprene and isobutene contributed most to ozone formation. Three methods were applied to evaluate O3-VOCs-NOx sensitivity in ZH: VOCs/NOx ratio method, Smog Production Model (SPM) and Relative Incremental Reactivity (RIR). The results show that summer ozone in urban Hangzhou mostly presents VOCs-limited and transition region alternately. Our study implies that the increasing automobiles and VOCs emissions from upwind area could result in ozone pollution in urban Hangzhou, and synergistic reduction of VOCs and NOx will be more effective.

Protection of plants from ambient ozone by applications of ethylenediurea (EDU): A meta-analytic review

International Nuclear Information System (INIS)

Feng Zhaozhong; Wang Shuguang; Szantoi, Zoltan; Chen Shuai; Wang Xiaoke

2010-01-01

A meta-analysis was conducted to quantitatively assess the effects of ethylenediurea (EDU) on ozone (O 3 ) injury, growth, physiology and productivity of plants grown in ambient air conditions. Results indicated that EDU significantly reduced O 3 -caused visible injury by 76%, and increased photosynthetic rate by 8%, above-ground biomass by 7% and crop yield by 15% in comparison with non-EDU treated plants, suggesting that ozone reduces growth and yield under current ambient conditions. EDU significantly ameliorated the biomass and yield of crops and grasses, but had no significant effect on tree growth with an exception of stem diameter. EDU applied as a soil drench at a concentration of 200-400 mg/L has the highest positive effect on crops grown in the field. Long-term research on full-grown tree species is needed. In conclusion, EDU is a powerful tool for assessing effects of ambient [O 3 ] on vegetation. - EDU effectively protect plants against ambient ozone.

Estimates of Free-tropospheric NO2 Abundance from the Aura Ozone Monitoring Instrument (OMI) Using Cloud Slicing Technique

Science.gov (United States)

Choi, S.; Joiner, J.; Krotkov, N. A.; Choi, Y.; Duncan, B. N.; Celarier, E. A.; Bucsela, E. J.; Vasilkov, A. P.; Strahan, S. E.; Veefkind, J. P.; Cohen, R. C.; Weinheimer, A. J.; Pickering, K. E.

2013-12-01

Total column measurements of NO2 from space-based sensors are of interest to the atmospheric chemistry and air quality communities; the relatively short lifetime of near-surface NO2 produces satellite-observed hot-spots near pollution sources including power plants and urban areas. However, estimates of NO2 concentrations in the free-troposphere, where lifetimes are longer and the radiative impact through ozone formation is larger, are severely lacking. Such information is critical to evaluate chemistry-climate and air quality models that are used for prediction of the evolution of tropospheric ozone and its impact of climate and air quality. Here, we retrieve free-tropospheric NO2 volume mixing ratio (VMR) using the cloud slicing technique. We use cloud optical centroid pressures (OCPs) as well as collocated above-cloud vertical NO2 columns (defined as the NO2 column from top of the atmosphere to the cloud OCP) from the Ozone Monitoring Instrument (OMI). The above-cloud NO2 vertical columns used in our study are retrieved independent of a priori NO2 profile information. In the cloud-slicing approach, the slope of the above-cloud NO2 column versus the cloud optical centroid pressure is proportional to the NO2 volume mixing ratio (VMR) for a given pressure (altitude) range. We retrieve NO2 volume mixing ratios and compare the obtained NO2 VMRs with in-situ aircraft profiles measured during the NASA Intercontinental Chemical Transport Experiment Phase B (INTEX-B) campaign in 2006. The agreement is good when proper data screening is applied. In addition, the OMI cloud slicing reports a high NO2 VMR where the aircraft reported lightning NOx during the Deep Convection Clouds and Chemistry (DC3) campaign in 2012. We also provide a global seasonal climatology of free-tropospheric NO2 VMR in cloudy conditions. Enhanced NO2 in free troposphere commonly appears near polluted urban locations where NO2 produced in the boundary layer may be transported vertically out of the

Geophysical validation of SCIAMACHY Limb Ozone Profiles

Directory of Open Access Journals (Sweden)

E. J. Brinksma

2006-01-01

Full Text Available We discuss the quality of the two available SCIAMACHY limb ozone profile products. They were retrieved with the University of Bremen IFE's algorithm version 1.61 (hereafter IFE, and the official ESA offline algorithm (hereafter OL versions 2.4 and 2.5. The ozone profiles were compared to a suite of correlative measurements from ground-based lidar and microwave, sondes, SAGE II and SAGE III (Stratospheric Aerosol and Gas Experiment. To correct for the expected Envisat pointing errors, which have not been corrected implicitly in either of the algorithms, we applied a constant altitude shift of -1.5 km to the SCIAMACHY ozone profiles. The IFE ozone profile data between 16 and 40 km are biased low by 3-6%. The average difference profiles have a typical standard deviation of 10% between 20 and 35 km. We show that more than 20% of the SCIAMACHY official ESA offline (OL ozone profiles version 2.4 and 2.5 have unrealistic ozone values, most of these are north of 15° S. The remaining OL profiles compare well to correlative instruments above 24 km. Between 20 and 24 km, they underestimate ozone by 15±5%.

Effect of pulsed corona discharge voltage and feed gas flow rate on dissolved ozone concentration

International Nuclear Information System (INIS)

Prasetyaningrum, A.; Ratnawati,; Jos, B.

2015-01-01

Ozonization is one of the methods extensively used for water purification and degradation of organic materials. Ozone (O 3 ) is recognized as a powerful oxidizing agent. Due to its strong oxidability and better environmental friendless, ozone increasing being used in domestic and industrial applications. Current technology in ozone production utilizes several techniques (corona discharge, ultra violet radiation and electrolysis). This experiment aimed to evaluating effect of voltage and gas flow rate on ozone production with corona discharge. The system consists of two net-type stainless steel electrode placed in a dielectric barrier. Three pulsed voltage (20, 30, 40 KV) and flow rate (5, 10, 15 L/min) were prepare for operation variable at high frequency (3.7 kHz) with AC pulsed power supply. The dissolved ozone concentration depends on the applied high-voltage level, gas flow rate and the discharge exposure duration. The ozone concentration increases with decreasing gas flow rate. Dissolved ozone concentrations greater than 200 ppm can be obtained with a minimum voltage 40 kV

Effect of pulsed corona discharge voltage and feed gas flow rate on dissolved ozone concentration

Science.gov (United States)

Prasetyaningrum, A.; Ratnawati, Jos, B.

2015-12-01

Ozonization is one of the methods extensively used for water purification and degradation of organic materials. Ozone (O3) is recognized as a powerful oxidizing agent. Due to its strong oxidability and better environmental friendless, ozone increasing being used in domestic and industrial applications. Current technology in ozone production utilizes several techniques (corona discharge, ultra violet radiation and electrolysis). This experiment aimed to evaluating effect of voltage and gas flow rate on ozone production with corona discharge. The system consists of two net-type stainless steel electrode placed in a dielectric barrier. Three pulsed voltage (20, 30, 40 KV) and flow rate (5, 10, 15 L/min) were prepare for operation variable at high frequency (3.7 kHz) with AC pulsed power supply. The dissolved ozone concentration depends on the applied high-voltage level, gas flow rate and the discharge exposure duration. The ozone concentration increases with decreasing gas flow rate. Dissolved ozone concentrations greater than 200 ppm can be obtained with a minimum voltage 40 kV.

Effect of pulsed corona discharge voltage and feed gas flow rate on dissolved ozone concentration

Energy Technology Data Exchange (ETDEWEB)

Prasetyaningrum, A., E-mail: ajiprasetyaningrum@gmail.com; Ratnawati,; Jos, B. [Department of Chemical Engineering, Faculty of Engineering, Diponegoro University Jl. Prof. H. Soedarto Tembalang, Semarang, Central Java, Indonesia, 50276 (Indonesia)

2015-12-29

Ozonization is one of the methods extensively used for water purification and degradation of organic materials. Ozone (O{sub 3}) is recognized as a powerful oxidizing agent. Due to its strong oxidability and better environmental friendless, ozone increasing being used in domestic and industrial applications. Current technology in ozone production utilizes several techniques (corona discharge, ultra violet radiation and electrolysis). This experiment aimed to evaluating effect of voltage and gas flow rate on ozone production with corona discharge. The system consists of two net-type stainless steel electrode placed in a dielectric barrier. Three pulsed voltage (20, 30, 40 KV) and flow rate (5, 10, 15 L/min) were prepare for operation variable at high frequency (3.7 kHz) with AC pulsed power supply. The dissolved ozone concentration depends on the applied high-voltage level, gas flow rate and the discharge exposure duration. The ozone concentration increases with decreasing gas flow rate. Dissolved ozone concentrations greater than 200 ppm can be obtained with a minimum voltage 40 kV.

Issues in Stratospheric Ozone Depletion.

Science.gov (United States)

Lloyd, Steven Andrew

Following the announcement of the discovery of the Antarctic ozone hole in 1985 there have arisen a multitude of questions pertaining to the nature and consequences of polar ozone depletion. This thesis addresses several of these specific questions, using both computer models of chemical kinetics and the Earth's radiation field as well as laboratory kinetic experiments. A coupled chemical kinetic-radiative numerical model was developed to assist in the analysis of in situ field measurements of several radical and neutral species in the polar and mid-latitude lower stratosphere. Modeling was used in the analysis of enhanced polar ClO, mid-latitude diurnal variation of ClO, and simultaneous measurements of OH, HO_2, H_2 O and O_3. Most importantly, such modeling was instrumental in establishing the link between the observed ClO and BrO concentrations in the Antarctic polar vortex and the observed rate of ozone depletion. The principal medical concern of stratospheric ozone depletion is that ozone loss will lead to the enhancement of ground-level UV-B radiation. Global ozone climatology (40^circS to 50^ circN latitude) was incorporated into a radiation field model to calculate the biologically accumulated dosage (BAD) of UV-B radiation, integrated over days, months, and years. The slope of the annual BAD as a function of latitude was found to correspond to epidemiological data for non-melanoma skin cancers for 30^circ -50^circN. Various ozone loss scenarios were investigated. It was found that a small ozone loss in the tropics can provide as much additional biologically effective UV-B as a much larger ozone loss at higher latitudes. Also, for ozone depletions of > 5%, the BAD of UV-B increases exponentially with decreasing ozone levels. An important key player in determining whether polar ozone depletion can propagate into the populated mid-latitudes is chlorine nitrate, ClONO_2 . As yet this molecule is only indirectly accounted for in computer models and field

Chloroplastic and stomatal aspects of ozone-induced reduction of net photosynthesis in plants

Energy Technology Data Exchange (ETDEWEB)

Torsethaugen, Gro

1998-09-01

The present thesis relates to ozone-induced reduction of photosynthesis in plants. As a photochemical oxidant O{sub 3} is formed by the interaction of hydrocarbons, nitrogen oxides and oxygen in sunlight. Ozone (O{sub 3}) is the most phytotoxic of all the air pollutants and is known to reduce plant growth and net photosynthesis, cause stomatal closure, induce visible injury, accelerate senescence and induce or inhibit transcription of a variety of genes with a corresponding increase/decrease in protein products. The underlying cellular mechanisms for many of these changes are unknown. Following fields are investigated: Ozone-induced reduction of net photosynthesis; ozone and the photosynthetic apparatus in the chloroplasts; ozone and stomata; ozone effects on plant membranes; protection against ozone injury in plants. 249 refs., 22 figs., 4 tabs.

First Reprocessing of Southern Hemisphere ADditional OZonesondes Profile Records: 3. Uncertainty in Ozone Profile and Total Column

Science.gov (United States)

Witte, Jacquelyn C.; Thompson, Anne M.; Smit, Herman G. J.; Vömel, Holger; Posny, Françoise; Stübi, Rene

2018-03-01

Reprocessed ozonesonde data from eight SHADOZ (Southern Hemisphere ADditional OZonesondes) sites have been used to derive the first analysis of uncertainty estimates for both profile and total column ozone (TCO). The ozone uncertainty is a composite of the uncertainties of the individual terms in the ozone partial pressure (PO3) equation, those being the ozone sensor current, background current, internal pump temperature, pump efficiency factors, conversion efficiency, and flow rate. Overall, PO3 uncertainties (ΔPO3) are within 15% and peak around the tropopause (15 ± 3 km) where ozone is a minimum and ΔPO3 approaches the measured signal. The uncertainty in the background and sensor currents dominates the overall ΔPO3 in the troposphere including the tropopause region, while the uncertainties in the conversion efficiency and flow rate dominate in the stratosphere. Seasonally, ΔPO3 is generally a maximum in the March-May, with the exception of SHADOZ sites in Asia, for which the highest ΔPO3 occurs in September-February. As a first approach, we calculate sonde TCO uncertainty (ΔTCO) by integrating the profile ΔPO3 and adding the ozone residual uncertainty, derived from the McPeters and Labow (2012, doi:10.1029/2011JD017006) 1σ ozone mixing ratios. Overall, ΔTCO are within ±15 Dobson units (DU), representing 5-6% of the TCO. Total Ozone Mapping Spectrometer and Ozone Monitoring Instrument (TOMS and OMI) satellite overpasses are generally within the sonde ΔTCO. However, there is a discontinuity between TOMS v8.6 (1998 to September 2004) and OMI (October 2004-2016) TCO on the order of 10 DU that accounts for the significant 16 DU overall difference observed between sonde and TOMS. By comparison, the sonde-OMI absolute difference for the eight stations is only 4 DU.

Ozone Effects on Fruit Productivity and Photosynthetic Response of Two Tomato Cultivars in Relation to Stomatal Fluxes

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Giacomo Gerosa

Full Text Available An Open-Top Chamber experiment on two tomato cultivars (cv. Oxheart and cv. San Marzano was carried out in Curno (Northern Italy between June and September 2007. Two ozone treatments were applied for a 3.5 months period: Non-Filtered OTC (NF-OTC, 95% of ambient ozone and Charcoal-Filtered OTC (CF-OTC, 50% of ambient ozone. Diurnal cycles of porometry measurements were performed during the season and allowed to draw a stomatal conductance model for each cultivar in order to calculate the ozone stomatal fluxes taken up by plants. Assessments on fruits yield were performed during the season, taking into account the number of fruits, their fresh weight and their marketability. In addition, measurements on the chlorophyll fluorescence of photosystems were carried out to assess possible negative effects on photosynthetic efficiency. Despite the two cultivars absorbed a similar ozone stomatal dose during the season (with an 8% difference, their responses to ozone treatments were totally divergent in relation to both fruits yield and photosynthetic efficiency. Plants of cv. Oxheart grown in NF-OTCs showed significant yield loss in the total weight of fruits (-35.9% which is exclusively related to a decrease in the number of fruits produced (-35.7% of total fruits; -30.6% of marketable fruits, since mean fresh weight of fruits remained unaffected. Moreover the same plants displayed low values (in comparison to CF-OTCs plants of the photosynthetic efficiency index (PIabs during the most intense period of ozone stress (July occurred in the flowering stage of plants and at the beginning of fructification. Plants of the cv. San Marzano had an opposite response behaviour with an increase of the mean fresh weight of fruits in plants grown in NF-OTC (even if not statistically significant and no difference in the number of fruits produced and in the values of photosynthetic efficiency.

Effect of ozone on leaf cell membranes

Energy Technology Data Exchange (ETDEWEB)

Swanson, E S; Thomson, W W; Mudd, J B

1973-01-01

The objective of this study was to determine the effects of ozone on membrane lipids and on the electron-density patterns of cell membranes in electron micrographs. Analysis of fatty acids from tobacco leaves fumigated with ozone indicated that there was no significant difference between the ozone-treated and the control plants in the relative amounts of the fatty acids. This suggests that if the primary site of ozone action is unsaturated lipids in membranes then the amounts of affected unsaturated fatty acids are too small to be detected by gas chromatography. In support of this, characteristic electron-microscopic images of membranes are observed in cells of fumigated leaves. However, measurements of the length and width of the chloroplasts and the determination of axial ratios indicated that the ozone treatment resulted in a shrinkage of the chloroplasts. In contrast, mitochondrial changes are apparently explained in terms of ozone-induced swelling. 33 references, 3 figures, 1 table.

Effect of increased carbon dioxide concentrations on stratospheric ozone

International Nuclear Information System (INIS)

Boughner, R.E.

1978-01-01

During the past several years, much attention has been focused on the destruction of ozone by anthropogenic pollutants such as the nitrogen oxides and chlorofluoromethane. Little or no attention has been given to the influence on ozone of an increased carbon dioxide concentration for which a measurable growth has been observed. Increased carbon dioxide can directly affect ozone by perturbing atmospheric temperatures, which will alter ozone production, whose rate displays a fairly strong temperature dependence. This paper presents one-dimensional model results for the steady state ozone behavior when the CO 2 concentration is twice its ambient level which account for coupling between chemistry and temperature. When the CO 2 level doubled, the total ozone burden increased in relation to the ambient burden by 1.2--2.5%, depending on the vertical diffusion coefficient used. Above 30 km. In this region the relation variations were insensitive to the choice of diffusion coefficient. Below 30 km, ozone concentrations were smaller than the unperturbed values and were sensitive to the vertical diffusion profile in this region (10--30 km). Ozone decreases in the lower stratosphere because of a reduction in ozone-producing solar radiation, which results in smaller downward ozone fluxes from the region at 25--30 km relative to the flux values for the ambient atmosphere. These offsetting changes occurring in the upper and lower stratosphere act to minimize the variation in total ozone

Atmospheric lifetimes and Ozone Depletion Potentials of trans-1-chloro-3,3,3-trifluoropropylene and trans-1,2-dichloroethylene in a three-dimensional model

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K. O. Patten

2010-11-01

Full Text Available The chloroalkenes trans-1-chloro-3,3,3-trifluoropropylene (tCFP and trans-1,2-dichloroethylene (tDCE have been proposed as candidate replacements for other compounds in current use that cause concerns regarding potential environmental effects including destruction of stratospheric ozone. Because tCFP and tDCE contain chlorine atoms, the effects of these short-lived compounds on stratospheric ozone must be established. In this study, we derive the atmospheric lifetimes and Ozone Depletion Potentials (ODPs for tCFP and for tDCE assuming emissions from land surfaces at latitudes 30° N to 60° N using the MOZART 3 three-dimensional model of atmospheric chemistry and physics. 53% of the ozone loss due to tCFP and 98% of the ozone loss due to tDCE take place in the troposphere, rather than in the stratosphere as generally expected from longer-lived chlorocarbons. The atmospheric lifetime of tCFP against chemical reaction is 40.4 days, and its ODP is quite small at 0.00034. The tDCE atmospheric lifetime is 12.7 days, and its ODP is 0.00024, which is the lowest ODP found for any chlorocarbon we have studied. Our study suggests that chlorine from tCFP and tDCE are unlikely to affect ozone at quantities likely to be emitted to the atmosphere.

Inhibiting the regeneration of N-nitrosodimethylamine in drinking water by UV photolysis combined with ozonation

Energy Technology Data Exchange (ETDEWEB)

Bingbing, Xu [State Key Laboratory of Urban Water Resource and Environment, School of Municipal and Environmental Engineering, Harbin Institute of Technology, Harbin, 150090 (China); State Environmental Protection Key Laboratory for Lake Pollution Control, Chinese Research Academy of Environmental Sciences, Beijing, 100012 (China); Chen Zhonglin, E-mail: zhonglinchen@263.net [State Key Laboratory of Urban Water Resource and Environment, School of Municipal and Environmental Engineering, Harbin Institute of Technology, Harbin, 150090 (China); Fei, Qi [College of Environmental Science and Engineering, Beijing Forestry University, Beijing, 100083 (China); Jun, Ma [State Key Laboratory of Urban Water Resource and Environment, School of Municipal and Environmental Engineering, Harbin Institute of Technology, Harbin, 150090 (China); Fengchang, Wu [State Environmental Protection Key Laboratory for Lake Pollution Control, Chinese Research Academy of Environmental Sciences, Beijing, 100012 (China)

2009-08-30

N-Nitrosodimethylamine (NDMA) is a highly carcinogenic compound that is suspected of carcinogenic activity in the human body. A variety of methods are used to remove NDMA from water, but the main degradation products, dimethylamine (DMA) and NO{sub 2}{sup -}, are also precursors for NDMA formation. UV irradiation combined with ozonation (UV/O{sub 3}) was examined in this investigation for its ability to inhibit the regeneration of NDMA after degradation. Both the degradation products and the regeneration potential of NDMA were compared between UV irradiation alone and UV/O{sub 3}. The yields of DMA and NO{sub 2}{sup -} in the UV/O{sub 3} process were less than for UV irradiation alone. Yields of DMA and NO{sub 2}{sup -} were 2.25 mg L{sup -1} and 3.22 mg L{sup -1} from UV irradiation, while they were 0.92 mg L{sup -1} and 0.45 mg L{sup -1} from the UV/O{sub 3} process. Furthermore, the regeneration of NDMA was also less after the UV/O{sub 3} process than after UV irradiation. The concentration of regenerated NDMA was more than 51.8 {mu}g L{sup -1} after UV irradiation regardless of the dosage of Cl{sub 2}. However, the concentration of regenerated NDMA in the UV/O{sub 3} process was less than 7.37 {mu}g L{sup -1} under the same conditions. Consequently, the UV/O{sub 3} process was more effective than UV irradiation alone in inhibiting NDMA regeneration. The inhibition of NDMA regeneration was due to a decrease in DMA and NO{sub 2}{sup -} produced by the UV/O{sub 3} process. As the major products generated from NDMA, NO{sub 2}{sup -} and DMA were likely to be oxidized by ozone and hydroxyl radicals ({center_dot}OH). In addition, the reaction between NDMA and {center_dot}OH would possibly generate methylamine as the only product, leading to a decrease in the production of DMA by the UV/O{sub 3} process.

Impact of near-surface atmospheric composition on ozone formation in Russia

Science.gov (United States)

Berezina, Elena; Moiseenko, Konstantin; Skorokhod, Andrey; Belikov, Igor; Pankratova, Natalia; Elansky, Nikolai

2017-04-01

One of the consequences of the human impact on the atmosphere is increasing in tropospheric ozone concentration, with the highest ozone level being observed in industrially developed and highly populated regions of the world. In these regions, main anthropogenic sources of carbon monoxide (CO), methane (CH4) and volatile organic compounds (VOCs) are concentrated. The oxidation of these compounds, when interacting with hydroxyl and nitrogen oxides at rather high temperature and sunlight, leads to ozone formation. CO and CH4 are slowly oxidized in the atmosphere and cause an increase in global and regional background ozone. However, the oxidation of some VOCs occurs during daylight hours and is accompanied by an increase in ozone concentration near VOCs sources, particularly in urban and industrial areas. The contribution of biogenic VOCs to ozone generation is estimated to be from 40 to 70% of the total contribution of all chemical ozone precursors in the troposphere [1], with isoprene playing the main role in ozone formation [2]. The impact of aromatic hydrocarbons to ozone formation is reported to be about 40% of the total ozone generation from the oxidation of anthropogenic VOCs [3]. In this study, the results of VOCs measurements (isoprene, benzene, toluene, phenol, styrene, xylene and propilbenzene) by proton mass spectrometry in different regions of Russia along the Trans-Siberian railway from Moscow to Vladivostok from TROICA-12 campaign on a mobile laboratory in summer 2008 are analyzed. It is shown that the TROICA-12 measurements were carried out mostly in moderately polluted (2≤NOx20 ppb) conditions ( 20 and 2% of measurements, correspondingly). The lower troposphere chemical regime in the campaign is found to be mainly NOx sensitive, both in rural and urban environments, with typical morning NMHC/NOx ratios being well above 20. Hence, ozone production rates are expected to be controlled by regional NOx emissions and their complex interplay with both

Combined treatment of mezcal vinasses by ozonation and activated sludge.

Science.gov (United States)

2017-10-18

In Mexico, mezcal production generates huge amounts of vinasses (MV) that cause negative environmental impacts. Thus, MV treatment is necessary before discharge to water bodies. Although there is no information for mezcal vinasses, similar effluents have been treated by biological processes (i.e. anaerobic and aerobic) usually complemented by oxidative chemical pretreatments (ozonation) and physico-chemical methods. In this work MV were first ozonated and followed by batch aerobic biological degradation. In the ozonation stage, organic matter removals were 4.5-11 % as COD, whereas the removal of aromatic compounds and phenols were 16-32 % and 48-83 % respectively. In the aerobic post-treatment, COD depletions up to 85 % were achieved; removals in ozone pre-treated vinasses were higher (80 to 85 %) than that of raw vinasse (69 %). It seems that ozonation preferentially attacked the recalcitrant fraction of organic matter present in the vinasses and increased its aerobic biodegradability.

Outlooks for the development of ozone-safe refrigerant production at the Minatom facilities

International Nuclear Information System (INIS)

Shatalov, V.V.; Orekhov, V.T.; Dedov, A.S.; Zakharov, V.Yu.; Golubev, A.N.; Tsarev, V.A.

2001-01-01

Results of activities undertaken at the All-Russian Research Institute of Chemical Technology since 1988, which were aimed at search of new methods of synthesis of ozone-safe refrigerants, using depleted uranium hexafluoride waste formed at gas-diffusion plants as fluorinating agent, are considered. It is pointed out that major advantages of the flowsheets making use of UF 6 versus traditional method consist in the fact that the processes are conducted in gas phase under normal pressure and moderate temperatures with UF 6 transfer into a more environmentally friendly form. Outlooks for expansion of production of ozone-safe refrigerants by the method described are discussed [ru

Effect of isoprene emissions from major forests on ozone formation in the city of Shanghai, China

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F. Geng

2011-10-01

Full Text Available Ambient surface level concentrations of isoprene (C₅H₈ were measured in the major forest regions located south of Shanghai, China. Because there is a large coverage of broad-leaved trees in this region, high concentrations of isoprene were measured, ranging from 1 to 6 ppbv. A regional dynamical/chemical model (WRF-Chem is applied for studying the effect of such high concentrations of isoprene on the ozone production in the city of Shanghai. The evaluation of the model shows that the calculated isoprene concentrations agree with the measured concentrations when the measured isoprene concentrations are lower than 3 ppb, but underestimate the measurements when the measured values are higher than 3 ppb. Isoprene was underestimated only at sampling sites near large bamboo plantations, a high isoprene source, indicating the need to include geospatially resolved bamboo distributions in the biogenic emission model. The assessment of the impact of isoprene on ozone formation suggests that the concentrations of peroxy radicals (RO₂ are significantly enhanced due to the oxidation of isoprene, with a maximum of 30 ppt. However, the enhancement of RO₂ is confined to the forested regions. Because the concentrations of NO_x were low in the forest regions, the ozone production due to the oxidation of isoprene (C₅H₈ + OH → → RO₂ + NO → → O₃ is low (less than 2–3 ppb h⁻¹. The calculation further suggests that the oxidation of isoprene leads to the enhancement of carbonyls (such as formaldehyde and acetaldehyde in the regions downwind of the forests, due to continuous oxidation of isoprene in the forest air. As a result, the concentrations of HO₂ radical are enhanced, resulting from the photo-disassociation of formaldehyde and acetaldehyde. Because the enhancement of HO₂ radical occurs in regions downwind of the forests

Quality assessment of the Ozone_cci Climate Research Data Package (release 2017 – Part 1: Ground-based validation of total ozone column data products

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K. Garane

2018-03-01

Full Text Available The GOME-type Total Ozone Essential Climate Variable (GTO-ECV is a level-3 data record, which combines individual sensor products into one single cohesive record covering the 22-year period from 1995 to 2016, generated in the frame of the European Space Agency's Climate Change Initiative Phase II. It is based on level-2 total ozone data produced by the GODFIT (GOME-type Direct FITting v4 algorithm as applied to the GOME/ERS-2, OMI/Aura, SCIAMACHY/Envisat and GOME-2/Metop-A and Metop-B observations. In this paper we examine whether GTO-ECV meets the specific requirements set by the international climate–chemistry modelling community for decadal stability long-term and short-term accuracy. In the following, we present the validation of the 2017 release of the Climate Research Data Package Total Ozone Column (CRDP TOC at both level 2 and level 3. The inter-sensor consistency of the individual level-2 data sets has mean differences generally within 0.5 % at moderate latitudes (±50°, whereas the level-3 data sets show mean differences with respect to the OMI reference data record that span between −0.2 ± 0.9 % (for GOME-2B and 1.0 ± 1.4 % (for SCIAMACHY. Very similar findings are reported for the level-2 validation against independent ground-based TOC observations reported by Brewer, Dobson and SAOZ instruments: the mean bias between GODFIT v4 satellite TOC and the ground instrument is well within 1.0 ± 1.0 % for all sensors, the drift per decade spans between −0.5 % and 1.0 ± 1.0 % depending on the sensor, and the peak-to-peak seasonality of the differences ranges from ∼ 1 % for GOME and OMI to  ∼ 2 % for SCIAMACHY. For the level-3 validation, our first goal was to show that the level-3 CRDP produces findings consistent with the level-2 individual sensor comparisons. We show a very good agreement with 0.5 to 2 % peak-to-peak amplitude for the monthly mean difference time series and a

Cr(VI) formation during ozonation of Cr-containing materials in ...

African Journals Online (AJOL)

Ozonation, or advanced oxidation processes (utilising ozone decomposition products as oxidants) are widely used in industrial wastewater and drinking water treatment plants. In these applications the use of ozone is based on ozone and its decomposition by-products being strong oxidants. In this paper, the possible ...

Chemical and Spectral Characterization of The Ozonation Products of κ-Carrageenan

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Prasetyaningrum Aji

2018-01-01

Full Text Available Kappa (κ- carrageenan oligomers are known to have several biological activities. Recent progress in the development of modified κ-carrageenan has resulted low molecular of κ-carrageenan. Ozone is a powerful oxidant and considered for depolymerization of κ-carrageenan. However, few studies have investigated the changes in κ-carrageenan properties associated with ozone treatment. This study would investigate on the changes in chemical structure after ozonation process. The experiments were carried out in a glass reactor equipped with an ozone bubble diffuser. Ozone with concentration of 80 ± 2 was bubbled into the solution. The ozone treatment was conducted at different times, i.e., 0 (control, 5, 10, 15, and 20 minutes. The experiments were conducted at pH 7 and constant stirring speed (200 rpm. Ozone-treated κ-carrageenan was dried at 60 ºC for 24 h in a forced air oven. The chemical and spectral analyses of κ-carrageenan after ozonation process were carried out using UV-Vis and FT-IR spectroscopy. These changes are seen in the UV spectra as a high intensity of absorbance peak at 290 nm. It is shows that ozonation of κ-carrageenan leads to some chemical changes such as the formation of carbonyl, carboxyl or double bonds.The FT-IR spectra reveals that the chemical structure of degraded κ-carrageenan, in term of sulfate content, is only slightly affected by the ozone treatment.

Influence of local meteorology and NO2 conditions on ground-level ozone concentrations in the eastern part of Texas, USA

OpenAIRE

Gorai, A. K.; Tuluri, F.; Tchounwou, P. B.; Ambinakudige, S.

2015-01-01

The influence of local climatic factors on ground-level ozone concentrations is an area of increasing interest to air quality management in regards to future climate change. This study presents an analysis on the role of temperature, wind speed, wind direction, and NO2 level on ground-level ozone concentrations over the region of Eastern Texas, USA. Ozone concentrations at the ground level depend on the formation and dispersion processes. Formation process mainly depends on the precursor sour...

Modelling horizontal and vertical concentration profiles of ozone and oxides of nitrogen within high-latitude urban areas

International Nuclear Information System (INIS)

Nicholson, J.P.; Weston, K.J.

2001-01-01

Urban ozone concentrations are determined by the balance between ozone destruction, chemical production and supply through advection and turbulent down-mixing from higher levels. At high latitudes, low levels of solar insolation and high horizontal advection speeds reduce the photochemical production and the spatial ozone concentration patterns are largely determined by the reaction of ozone with nitric oxide and dry deposition to the surface. A Lagrangian column model has been developed to simulate the mean (monthly and annual) three-dimensional structure in ozone and nitrogen oxides (NO x ) concentrations in the boundary-layer within and immediately around an urban area. The short-time-scale photochemical processes of ozone and NO x , as well as emissions and deposition to the ground, are simulated. The model has a horizontal resolution of 1x1km and high resolution in the vertical. It has been applied over a 100x100km domain containing the city of Edinburgh (at latitude 56 o N) to simulate the city-scale processes of pollutants. Results are presented, using averaged wind-flow frequencies and appropriate stability conditions, to show the extent of the depletion of ozone by city emissions. The long-term average spatial patterns in the surface ozone and NO x concentrations over the model domain are reproduced quantitatively. The model shows the average surface ozone concentrations in the urban area to be lower than the surrounding rural areas by typically 50% and that the areas experiencing a 20% ozone depletion are generally restricted to within the urban area. The depletion of the ozone concentration to less than 50% of the rural surface values extends only 20m vertically above the urban area. A series of monitoring sites for ozone, nitric oxide and nitrogen dioxide on a north-south transect through the city - from an urban, through a semi-rural, to a remote rural location - allows the comparison of modelled with observed data for the mean diurnal cycle of ozone

Nicotiana tabacum as model for ozone - plant surface reactions

Science.gov (United States)

Jud, Werner; Fischer, Lukas; Wohlfahrt, Georg; Tissier, Alain; Canaval, Eva; Hansel, Armin

2015-04-01

Elevated tropospheric ozone concentrations are considered a toxic threat to plants, responsible for global crop losses with associated economic costs of several billion dollars per year. The ensuing injuries have been related to the uptake of ozone through the stomatal pores and oxidative effects damaging the internal leaf tissue. A striking question of current research is the environment and plant specific partitioning of ozone loss between gas phase, stomatal or plant surface sink terms. Here we show results from ozone fumigation experiments using various Nicotiana Tabacum varieties, whose surfaces are covered with different amounts of unsaturated diterpenoids exuded by their glandular trichomes. Exposure to elevated ozone levels (50 to 150 ppbv) for 5 to 15 hours in an exceptionally clean cuvette system did neither result in a reduction of photosynthesis nor caused any visible leaf damage. Both these ozone induced stress effects have been observed previously in ozone fumigation experiments with the ozone sensitive tobacco line Bel-W3. In our case ozone fumigation was accompanied by a continuous release of oxygenated volatile organic compounds, which could be clearly associated to their condensed phase precursors for the first time. Gas phase reactions of ozone were avoided by choosing a high enough gas exchange rate of the plant cuvette system. In the case of the Ambalema variety, that is known to exude only the diterpenoid cis-abienol, ozone fumigation experiments yield the volatiles formaldehyde and methyl vinyl ketone (MVK). The latter could be unequivocally separated from isomeric methacrolein (MACR) by the aid of a Selective Reagent Ion Time-of-Flight Mass Spectrometer (SRI-ToF-MS), which was switched every six minutes from H3O+ to NO+ primary ion mode and vice versa. Consistent with the picture of an ozone protection mechanism caused by reactive diterpenoids at the leaf surface are the results from dark-light experiments. The ozone loss obtained from the