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Sample records for in-cloud so2 oxidation

  1. Redox Equilibria in SO2 Oxidation Catalysts

    DEFF Research Database (Denmark)

    Rasmussen, Søren Birk; Eriksen, Kim Michael; Boghosian, Soghomon

    1999-01-01

    The catalyst used for sulfuric acid production is well described by the molten salt-gas system M2S2O7-V2O5/SO2-O2-SO3-N2 (M=Na, K, Cs) at 400 - 600°C.In order to understand the mechanism of the oxidation of SO2 by O2 to SO3, catalyzed by the above mentioned system, rather intensive research has...... been carried out regarding the complex and compound formation of V(V) and the formation of V(IV) and V(III) compounds with low solubility causing catalyst deactivation. However, the redox chemistry of vanadium and the complex formation of V(IV) is much less investigated and further information...

  2. Impacts of Four SO2 Oxidation Pathways on Wintertime Sulfate Concentrations

    Science.gov (United States)

    Sarwar, G.; Fahey, K.; Zhang, Y.; Kang, D.; Mathur, R.; Xing, J.; Wei, C.; Cheng, Y.

    2017-12-01

    Air quality models tend to under-estimate winter-time sulfate concentrations compared to observed data. Such under-estimations are particularly acute in China where very high concentrations of sulfate have been measured. Sulfate is produced by oxidation of sulfur dioxide (SO2) in gas-phase by hydroxyl radical and in aqueous-phase by hydrogen peroxide, ozone, etc. and most air quality models employ such typical reactions. Several additional SO2 oxidation pathways have recently been proposed. Heterogeneous reaction on dust has been suggested to be an important sink for SO2. Oxidation of SO2 on fine particles in presence of nitrogen dioxide (NO2) and ammonia (NH3) at high relative humidity has been implicated for sulfate formation in Chinese haze and London fog. Reactive nitrogen chemistry in aerosol water has also been suggested to produce winter-time sulfate in China. Specifically, high aerosol water can trap SO2 which can be subsequently oxidized by NO2 to form sulfate. Aqueous-phase (in-cloud) oxidation of SO2 by NO2 can also produce sulfate. Here, we use the hemispheric Community Multiscale Air Quality (CMAQ) modeling system to examine the potential impacts of these SO2 oxidation pathways on sulfate formation. We use anthropogenic emissions from the Emissions Database for Global Atmospheric Research and biogenic emissions from Global Emissions InitiAtive. We performed simulations without and with these SO2 oxidation pathways for October-December of 2014 using meteorological fields obtained from the Weather Research and Forecasting model. The standard CMAQ model contains one gas-phase chemical reaction and five aqueous-phase chemical reactions for SO2 oxidation. We implement four additional SO2 oxidation pathways into the CMAQ model. Our preliminary results suggest that the dust chemistry enhances mean sulfate over parts of China and Middle-East, the in-cloud SO2 oxidation by NO2 enhances sulfate over parts of western Europe, oxidation of SO2 by NO2 and NH3 on

  3. SO2 oxidation catalyst model systems characterized by thermal methods

    DEFF Research Database (Denmark)

    Hatem, G; Eriksen, Kim Michael; Gaune-Escard, M

    2002-01-01

    ) and Differential Scanning Calorimetry (DSC). Fundamental thermodynamic data like temperatures and molar heats of solid-solid transition and fusion, phase diagrams, heat capacities of solids and liquids, heat of mixing and heats of complex formation have been obtained and the results are discussed in relation...... to the mechanism Of SO2 oxidation by V2O5 based industrial catalysts....

  4. High-throughput technology for novel SO2 oxidation catalysts

    Science.gov (United States)

    Loskyll, Jonas; Stoewe, Klaus; Maier, Wilhelm F.

    2011-10-01

    We review the state of the art and explain the need for better SO2 oxidation catalysts for the production of sulfuric acid. A high-throughput technology has been developed for the study of potential catalysts in the oxidation of SO2 to SO3. High-throughput methods are reviewed and the problems encountered with their adaptation to the corrosive conditions of SO2 oxidation are described. We show that while emissivity-corrected infrared thermography (ecIRT) can be used for primary screening, it is prone to errors because of the large variations in the emissivity of the catalyst surface. UV-visible (UV-Vis) spectrometry was selected instead as a reliable analysis method of monitoring the SO2 conversion. Installing plain sugar absorbents at reactor outlets proved valuable for the detection and quantitative removal of SO3 from the product gas before the UV-Vis analysis. We also overview some elements used for prescreening and those remaining after the screening of the first catalyst generations.

  5. High-throughput technology for novel SO2 oxidation catalysts

    Directory of Open Access Journals (Sweden)

    Jonas Loskyll, Klaus Stoewe and Wilhelm F Maier

    2011-01-01

    Full Text Available We review the state of the art and explain the need for better SO2 oxidation catalysts for the production of sulfuric acid. A high-throughput technology has been developed for the study of potential catalysts in the oxidation of SO2 to SO3. High-throughput methods are reviewed and the problems encountered with their adaptation to the corrosive conditions of SO2 oxidation are described. We show that while emissivity-corrected infrared thermography (ecIRT can be used for primary screening, it is prone to errors because of the large variations in the emissivity of the catalyst surface. UV-visible (UV-Vis spectrometry was selected instead as a reliable analysis method of monitoring the SO2 conversion. Installing plain sugar absorbents at reactor outlets proved valuable for the detection and quantitative removal of SO3 from the product gas before the UV-Vis analysis. We also overview some elements used for prescreening and those remaining after the screening of the first catalyst generations.

  6. Oxidation behavior of molten magnesium in atmospheres containing SO2

    International Nuclear Information System (INIS)

    Wang Xianfei; Xiong Shoumei

    2011-01-01

    Graphical abstract: Highlights: → We found the film formed on molten magnesium had a two or three layers structure. → The formation mechanism of film was investigated and a growth model was proposed. → We found the formation of MgSO 4 was critical and promoted the growth of the film. - Abstract: The microchemistry and morphology of the oxide layer formed on molten magnesium in atmospheres containing SO 2 were examined. Based on the results and the thermodynamic and kinetic calculations of oxide-growth process, a schematic oxidation mechanism is presented. The results showed that the oxide scales with network structure were generally composed of MgO, MgS, and MgSO 4 with different layers, depending on the SO 2 content, the time and the temperature. The formation of MgSO 4 was important for the formation of the protective oxide scales. The growth of the oxide scales followed the parabolic law at 973 K and was controlled by diffusion.

  7. SO2 oxidation catalyst model systems characterized by thermal methods

    DEFF Research Database (Denmark)

    Hatem, G; Eriksen, Kim Michael; Gaune-Escard, M

    2002-01-01

    The molten salts M2S2O7 and MHSO4, the binary molten salt Systems M2S2O7-MHSO4 and the molten salt-gas systems M2S2O7 V2O5 and M2S2O7-M2SO4 V2O5 (M = Na, K, Rb, Cs) in O-2, SO2 and At atmospheres have been investigated by thermal methods like calorimetry, Differential Enthalpic Analysis (DEA......) and Differential Scanning Calorimetry (DSC). Fundamental thermodynamic data like temperatures and molar heats of solid-solid transition and fusion, phase diagrams, heat capacities of solids and liquids, heat of mixing and heats of complex formation have been obtained and the results are discussed in relation...

  8. CHEMISTRY OF SO2 AND DESOX PROCESSES ON OXIDE NANOPARTICLES.

    Energy Technology Data Exchange (ETDEWEB)

    RODRIGUEZ, J.A.

    2006-06-30

    On bulk stoichiometric oxides, SO{sub 2} mainly reacts with the O centers to form SO{sub 3} or SO{sub 4} species that decompose at elevated temperatures. Adsorption on the metal cations occurs below 300 K and does not lead to cleavage of the S-O bonds. In bulk oxides, the occupied cation bands are too stable for effective bonding interactions with the LUMO of SO{sub 2}. The effects of quantum confinement on the electronic properties of oxide nanoparticles and the structural defects that usually accompany these systems in general favor the bonding and dissociation of SO{sub 2}. Thus, nanoparticles of MgO, CaO, SrO, Al{sub 2}O{sub 3}, Fe{sub 2}O{sub 3} and CeO{sub 2} are all more efficient for sequestering SO{sub 2} than the corresponding bulk oxides. Structural imperfections in pure or metal-doped ceria nanoparticles accelerate the reduction of SO{sub 2} by CO by facilitating the formation and migration of O vacancies in the oxide surface.

  9. Progress on the mechanistic understanding of SO2 oxidation catalysts

    DEFF Research Database (Denmark)

    Lapina, Olga B.; Bal'zhinimaev, B.S.; Boghosian, Soghomon

    1999-01-01

    For almost a century vanadium oxide based catalysts have been the dominant materials in industrial processes for sulfuric acid production. A vast body of information leading to fundamental knowledge on the catalytic process was obtained by Academician [G.K. Boreskov, Catalysis in Sulphuric Acid...... Production, Goskhimizdat (in Russian), Moscow, 1954, p. 348]. In recent years these catalysts have also been used to clean flue gases and other SO; containing, industrial off-gases. In spite of the importance and long utilization of these industrial processes, the catalytic active species and the reaction...... mechanism. A multiinstrumental investigation that combine the efforts of four groups from four different countries has been carried out on the model system as well as on working industrial catalysts. Detailed information has been obtained on the complex and on the redox chemistry of vanadium. Based on this...

  10. DFT studies on the heterogeneous oxidation of SO2 by oxygen functional groups on graphene.

    Science.gov (United States)

    He, Guangzhi; He, Hong

    2016-11-23

    The heterogeneous oxidation of SO 2 has been the subject of intense scrutiny in atmospheric chemistry because of the adverse effects of sulfate particles. Although it has been found that the soot particles with a graphene-like structure play an important role in the oxidation of SO 2 , little is known about the atomic-level mechanism involved. Here, we studied the oxidation of SO 2 on oxygen-functionalized graphene using density functional theory (DFT) calculation. The results showed that SO 2 is oxidized by the epoxide group via a two-step mechanism, where the C-O bond away from the SO 2 is broken first, followed by the breaking of the other C-O bond and the synchronous formation of a new S-O bond. The energy barriers are significantly decreased when solvation free energies are involved, suggesting that humidity is favorable for promoting the oxidation by reducing the reaction barrier. The energy barriers for H 2 SO 3 oxidation are much higher than that for SO 2 oxidation, indicating that the direct conversion of SO 2 to SO 3 is the main pathway for the oxidation of SO 2 by oxygen-functionalized graphene sheets in both the gas phase and solution. The reduced density gradient (RDG) analysis showed that the hydrogen bond formed between H 2 SO 3 and epoxide groups enhances the stability of the reaction complex, and is responsible for the high energy barrier that has to be overcome for the reaction to proceed. These atomistic studies proposed a two-step mechanism for the oxidation of SO 2 on the oxygen-functionalized graphene-like carbonaceous surfaces under ambient conditions.

  11. Physico-Chemical and Structural Properties of DeNOx and SO2 Oxidation Catalysts

    DEFF Research Database (Denmark)

    Masters, Stephen Grenville; Oehlers, Cord; Nielsen, Kurt

    1996-01-01

    Commercial catalysts for NOx removal and SO2 oxidation and their model systems have been investigated by spectroscopic, thermal, electrochemical and X-ray methods. Structural information on the vanadium complexes and compounds as well as physico-chemical properties for catalyst model systems have...

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

    Directory of Open Access Journals (Sweden)

    Bo Li

    2015-01-01

    Full Text Available 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.

  13. Electrochemical study on the cationic promotion of the catalytic SO2 oxidation in pyrosulfate melts

    DEFF Research Database (Denmark)

    Petrushina, Irina; Bjerrum, Niels; Cappeln, Frederik Vilhelm

    1998-01-01

    on the catalytic oxidation of SO2 in the V2O5-M2S2O7 system and the effect of these alkali cations on the electrochemical behavior of V2O5 in the alkali pyrosulfate melts It has been shown that Na+ ions had a promoting effect on the V(V) reversible arrow V(IV) electrochemical reaction. Sodium ions accelerate both...... in the catalytic SO, oxidation most likely is the oxidation of V(IV) to V(V) and the Na+ and Cs+ promoting effect is based on the acceleration of this stage. It has also been proposed that voltammetric measurements can be used for fast optimization of the composition of the vanadium catalyst (which...

  14. Adsorption and oxidation of SO2 by graphene oxides: A van der Waals density functional theory study

    Science.gov (United States)

    Zhang, Huijuan; Cen, Wanglai; Liu, Jie; Guo, Jiaxiu; Yin, Huaqiang; Ning, Ping

    2015-01-01

    Carbon materials have been used for low temperature (20-150 °C) catalytic removal of SO2 from the coal-burned flue gases for a long time, but the mechanism at atomic level is still controversial. Density functional theory was used to investigate the adsorption and oxidation of SO2 on elaborated graphene oxides (GOs) to discover the insights. It is found that the hydroxyl groups on GO surface possess bi-functional effects: both enhancing the adsorption of SO2 through H-bonding interaction and reducing the reaction barrier for its oxidation to SO3. The promotion of oxidation is related to a pre-activation of the surface epoxy group. Based on Bader population, charge difference and electron localization function analysis, a charge transfer channel is proposed to explain the pre-activation.

  15. Vanadia-silica and vanadia-cesium-silica catalysts for oxidation of SO2

    DEFF Research Database (Denmark)

    Pârvulescu, Vasile I.; Paun, Christina; Pârvulescu, Viorica

    2004-01-01

    Mesoporous vanadia-silica catalysts have been prepared by three different sol-gel procedures using tetraethylorthosilicate (TEOS), vanadyl acetylacetonate (VAA), or VOCl3 and in some cases quaternary ammonium salts ((CH3)(3)C14H29N+Br- or (C10H21)(4)N+Br-) as surfactants. According to procedure A......)-based industrial catalyst, where kieselghur is used as carrier material. The high dispersion of vanadium in the studied catalysts results in an increased catalytic activity for the oxidation of SO2 contained in feed gases with low SO2 content......., TEOS and VAA were concomitantly hydrolyzed, in procedure B TEOS was prehydrolized and vanadium precursor was added to the silica sol, and in procedure C both TEOS and vanadium precursors were separately prehydrolized. The sol-gel procedures were controlled by checking the effect of the hydrolysis p......H, refluxing time, surfactant, and conditions of gellifications (slow evaporation at room temperature or autoclavization). The samples were dried under vacuum, first at room temperature, then at 373 K, and finally calcined at 773 K. ICP-AES analysis indicated for all samples a vanadium content of around 6.5 wt...

  16. Vanadia-silica and vanadia-cesium-silica catalysts for oxidation of SO2

    DEFF Research Database (Denmark)

    Pârvulescu, Vasile I.; Paun, Christina; Pârvulescu, Viorica

    2004-01-01

    Mesoporous vanadia-silica catalysts have been prepared by three different sol-gel procedures using tetraethylorthosilicate (TEOS), vanadyl acetylacetonate (VAA), or VOCl3 and in some cases quaternary ammonium salts ((CH3)(3)C14H29N+Br- or (C10H21)(4)N+Br-) as surfactants. According to procedure A......)-based industrial catalyst, where kieselghur is used as carrier material. The high dispersion of vanadium in the studied catalysts results in an increased catalytic activity for the oxidation of SO2 contained in feed gases with low SO2 content.......Mesoporous vanadia-silica catalysts have been prepared by three different sol-gel procedures using tetraethylorthosilicate (TEOS), vanadyl acetylacetonate (VAA), or VOCl3 and in some cases quaternary ammonium salts ((CH3)(3)C14H29N+Br- or (C10H21)(4)N+Br-) as surfactants. According to procedure A......%. The samples were impregnated with Cs2SO4 resulting in a Cs:V ratio of 3:1 and then dried and calcined under the same conditions. The catalysts were characterized using several methods: sorption isotherms of N-2 at 77 K, XRD, and XPS. The results of the characterization indicated that during calcination...

  17. Oxidation of SO2 and formation of water droplets under irradiation of 20MeV protons in N2/H2O/SO2

    DEFF Research Database (Denmark)

    Tomita, Shigeo; Nakai, Yoichi; Funada, Shuhei

    2015-01-01

    We have performed an experiment on charged droplet formation in a humidified N2 gas with trace SO2 concentration and induced by 20MeV proton irradiation. It is thought that SO2 reacts with the chemical species, such as OH radicals, generated through the reactions triggered by N2+ production. Both...... droplets contributes to the formation of the droplets. The charged droplet volume detected per unit time is proportional to the SO2 consumption, which indicates that a constant amount of sulfur atoms is contained in a unit volume of droplet, regardless of different droplet-size distributions depending...

  18. Antioxidant defenses of mycorrhizal fungus infection against SO(2)-induced oxidative stress in Avena nuda seedlings.

    Science.gov (United States)

    Huang, L L; Yang, C; Zhao, Y; Xu, X; Xu, Q; Li, G Z; Cao, J; Herbert, S J; Hao, L

    2008-11-01

    Colonization of arbuscular mycorrhizal fungi Glomus mosseae increased Avena nuda seedling tolerance to SO(2) exposure, as indicated by elevated total plant biomass and ameliorative photosynthetic rate, when compared to the non-mycorrhizal plants. This is associated with an improved antioxidant capacity as shown by enhanced superoxide dismutase and catalase activity, increased ascorbic acid and glutathione content, and reduced malondialdehyde and hydrogen peroxide level in the mycorrhizal plants relative to the non-mycorrhizal plants under SO(2) exposure. The mycorrhizal fungi colonization had no effect on the stomatal conductance. To our knowledge, this is the first finding of this sort.

  19. Efficient Low-Temperature Oxidation of Carbon-Cluster Anions by SO2

    Science.gov (United States)

    Leavitt, Andrew; Wywras, Richard; Wallace, William; Serrano, Daniel; Arredondo, Melissa; Leslie, Logan; Khan, Farooq; Whetten, Robert

    2006-03-01

    Carbon-cluster anions, CN^-, are very reactive toward SO2 (sticking probability of 0.012 ± 0.005 for C27^- at 25 ^oC), in contrast to their inertness toward other common atmospheric gases and pollutants. In flow-reactor experiments at ambient temperature and near atmospheric pressure, primary adsorption of SO2 by the carbon cluster anions, N = 4 -- 60, yields CNSO2^- or CN-1S^-. The inferred elimination of neutral CO2 is also detected as meta-stable decay in collision-induced dissociation. At higher temperatures, the reaction of SO2 with nascent carbon clusters yields CN-1SO^- as well as undetected CO. Such carbon clusters are formed in sooting flames and may act as nuclei for the formation of primary soot particles, and serve as models for the local structural features of active soot particle sites for black-carbon soot. The facile generation of reactive carbon-sulfide and --sulfinate units may therefore have implications for understanding the health and environmental effects attributed to the coincidence of soot and SO2.

  20. Adsorption of O2, SO2, and SO3, on nickel oxide - Mechanism for sulfate formation

    Science.gov (United States)

    Mehandru, S. P.; Anderson, A. B.

    1986-01-01

    Calculations based on the atom superposition and electron delocalization molecular orbital technique suggest that O2 will adsorb preferentially end-on at an angle 45 deg from normal on a nickel cation site on the (100) surface of NiO. SO2 adsorption is also stronger on the nickel site; SO2 bonds through the sulfur atom in a plane perpendicular to the surface. Adsorption energies for SO3 on the nickel and oxygen sites are comparable in the preferred orientation in which the SO3 plane is parallel to the surface. The calculations suggest that the strength of adsorption varies as O2 greater than SO2 greater than SO3. On activation, SO3 adsorbed to an O(2-) site forms a trigonal pyramidal SO4 species which yields, with a low barrier, a tetrahedral sulfate anion. Subsequently the anion reorients on the surface. Alternative mechanisms which require the formation of Ni(3+) or O(-) are discussed. NiSO4 thus formed may play a passivating role for the corrosion of Ni at low temperatures in the SO2 + O2 + SO3 atmospheres and an active role at high temperatures, as discussed in the experimental literature.

  1. Adsorption of O2, SO2, and SO3 on nickel oxide. Mechanism for sulfate formation

    Science.gov (United States)

    Mehandru, S. P.; Anderson, A. B.

    1985-01-01

    Calculations based on the atom superposition and electron delocalization molecular orbital (ASED-MO) technique suggest that O2 will adsorb perferentially end-on at an angle 45 deg from normal on a nickel cation site on the (100) surface of NiO. SO2 adsorption is also stronger on the nickel site; SO2 bonds through the sulfur atom is a plane perpendicular to the surface. Adsorption energies for SO3 on the nickel and oxygen sites are comparable in the perferred orientation in which the SO3 plane is parallel to the surface. On activation, SO3 adsorbed to an O2(-) site forms a trigonal pyramidal SO4 species which yields, with a low barrier, a tetrahedral sulfate anion. Subsequently the anion reorients on the surface. Possibilities for alternative mechanisms which require the formation of Ni3(+) or O2(-) are discussed. NiSO4 thus formed leads to the corrosion of Ni at high temperatures in the SO2+O2/SO3 The SO2+O2/SO3 atmosphere, as discussed in the experimental literature.

  2. Importance of Vanadium-Catalyzed Oxidation of SO2to SO3in Two-Stroke Marine Diesel Engines

    DEFF Research Database (Denmark)

    Colom, Juan M.; Alzueta, María U.; Christensen, Jakob Munkholt

    2016-01-01

    Low-speed marine diesel engines are mostly operated on heavy fuel oils, which have a high content of sulfur andash, including trace amounts of vanadium, nickel, and aluminum. In particular, vanadium oxides could catalyze in-cylinderoxidation of SO2 to SO3, promoting the formation of sulfuric acid...... of the catalyticspecies within the engine. Experiments with different particle compositions (vanadium/sodium ratio) and temperatures (300−800 °C) show that both the temperature and sodium content have a major impact on the oxidation rate. Kinetic parameters forthe catalyzed reaction are determined, and the proposed...... kinetic model fits well with the experimental data. The impact of thecatalytic reaction is studied with a phenomenological zero-dimensional (0D) engine model, where fuel oxidation and SOxformation is modeled with a comprehensive gas-phase reaction mechanism. Results indicate that the oxidation of SO2...

  3. Promoting mechanism of N-doped single-walled carbon nanotubes for O2 dissociation and SO2 oxidation

    Science.gov (United States)

    Chen, Yanqiu; Yin, Shi; Chen, Yang; Cen, Wanglai; Li, Jianjun; Yin, Huaqiang

    2018-03-01

    Although heteroatom doping in carbon based catalysts have recently received intensive attentions, the role of the intrinsically porous structure of practical carbon materials and their potential synergy with doping atoms are still unclear. To investigate the complex effects, a range of N-doped single-walled carbon nanotubes (SWCNTs) were used to investigate their potential use for O2 dissociation and the subsequent SO2 oxidation using density functional theory. It is found that graphite N doping can synergize with the outer surface of SWCNTs to facilitate the dissociation of O2. The barrier for the dissociation on dual graphite N-doped SWCNT-(8, 8) is as low as 0.3 eV, and the subsequent SO2 oxidation is thermodynamically favorable and kinetically feasible. These results spotlight on developing promising carboncatalyst via utilization of porous gemometry and heteroatom-doping of carbon materials simultaneously.

  4. OH- Initiated Heterogeneous Oxidation of Saturated Organic Aerosols in the Presence of SO2: Uptake Kinetics and Product Identification.

    Science.gov (United States)

    Richards-Henderson, N. K.; Ward, M.; Goldstein, A. H.; Wilson, K. R.

    2014-12-01

    Gas-phase oxidation mechanisms for organic gases are often used as a starting point to understand heterogeneous oxidation. The reaction of a simple alkane hydrocarbon by OH proceeds through hydrogen abstraction and under ambient conditions leads to peroxy radical (RO2) formation. RO2 can further react to form: (1) smaller molecular weight products (i.e. fragmentation) via alkoxy radical formation and dissociation and/or (2) higher molecular weight products with oxygenated functional groups (i.e. functionalization). The ability to perturb these two pathways (functionalization vs. fragmentation) is critical for understanding the detailed reaction mechanism that control atmospheric aging chemistry of particles. At high temperatures the presence of sulfur dioxide (SO2) during organic-OH gas-phase oxidation enhances the fragmentation pathway leading to increased alkoxy formation. It is unknown if a comparative affect occurs at room temperature during a heterogeneous reaction. We used the heterogeneous reaction of OH radicals with sub-micron squalane particles in the presence and absence of SO2 as a model system to explore changes in individual mechanistic pathways. Detailed kinetic measurements were made in a flow tube reactor using a vacuum ultraviolet (VUV) photoionization aerosol mass spectrometer and oxidation products are identified from samples collected on quartz filters using thermal desorption two-dimensional chromatographic separation and ionization by either VUV (10.5 eV) or electron impact (70 eV), with detection by high resolution time of flight mass spectrometry (GCxGC-VUV/EI-HRTOFMS). In the presence of SO2 the yields of alcohols were enhanced compared to without SO2, suggesting that the alkoxy formation pathway was dominant. The results from this work will provide an experimentally-confirmed kinetic framework that could be used to model atmospheric aging mechanisms.

  5. Effects of SO2 oxidation on ambient aerosol growth in water and ethanol vapours

    Directory of Open Access Journals (Sweden)

    T. Petäjä

    2005-01-01

    Full Text Available Hygroscopicity (i.e. water vapour affinity of atmospheric aerosol particles is one of the key factors in defining their impacts on climate. Condensation of sulphuric acid onto less hygroscopic particles is expected to increase their hygrocopicity and hence their cloud condensation nuclei formation potential. In this study, differences in the hygroscopic and ethanol uptake properties of ultrafine aerosol particles in the Arctic air masses with a different exposure to anthropogenic sulfur pollution were examined. The main discovery was that Aitken mode particles having been exposed to polluted air were more hygroscopic and less soluble to ethanol than after transport in clean air. This aging process was attributed to sulphur dioxide oxidation and subsequent condensation during the transport of these particle to our measurement site. The hygroscopicity of nucleation mode aerosol particles, on the other hand, was approximately the same in all the cases, being indicative of a relatively similar chemical composition despite the differences in air mass transport routes. These particles had also been produced closer to the observation site typically 3–8 h prior to sampling. Apparently, these particles did not have an opportunity to accumulate sulphuric acid on their way to the site, but instead their chemical composition (hygroscopicity and ethanol solubility resembled that of particles produced in the local or semi-regional ambient conditions.

  6. Kinetics and mechanism of the oxidation of S(IV) by ozone in aqueous solution with particular reference to SO2 conversion in nonurban tropospheric clouds

    Science.gov (United States)

    Maahs, H. G.

    1983-01-01

    Results are presented from a laboratory study of the kinetics of the S(IV)-O3 reaction in aqueous solution, including measurements of the effects of UV radiation, dissolved transition metals, and an antioxidant (hydroquinone) on the rate. On the basis of the results, relative rates of S(IV) conversion by O3 in tropospheric cloud water are compared with those predicted for H2O2 and for O2. The reaction mechanism is discussed, with an outline given of the elements of a possible reaction scheme. Application of the rate constants obtained to SO2 conversion in cloud water predicts conversion rates by ozone to be competitive with those by H2O2 at pH above about 4.5 and to dominate at pH above about 5.5. It is pointed out that since these pH's are typical for nonurban tropospheric cloud water, ozone is a potentially important contributor to the overall oxidative conversion of SO2 to sulfate in the nonurban troposphere.

  7. REMOVAL OF SO2 AND NO OVER RICE HUSK ASH (RHA/CaO-SUPPORTED METAL OXIDES

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    IRVAN DAHLAN

    2008-08-01

    Full Text Available The activity of rice husk ash (RHA/CaO-based sorbent supported with various metal oxides for the removal of SO2 and NO from simulated flue gas of combustion process has been studied. In this study, RHA/CaO-based sorbents were impregnated with an appropriate metal nitrates solution followed by drying and calcinations, which resulted in the sorbent having the following active phases; MgO, MnO, CoO, ZnO, Al2O3, Fe2O3, and CeO2. The sorbent-catalysts were tested in a fixed bed reactor by passing mixture gas consisting of SO2 (2000 ppm, NO (500 ppm, O2 (10 %, water vapor (50% and N2 as a balance at a total flow rate of 150 mL/min and reaction temperature of 87C. The results showed that RHA/CaO sorbents impregnated with CeO2 displayed the highest sorption capacity among other impregnated metal oxides for the simultaneous removal of SO2 and NO. Infrared spectroscopic results indicate the formation of both sulfate (SO42- and nitrate (NO3- species due to a catalytic role played by CeO2.

  8. The atmospheric impacts of monoterpene ozonolysis on global stabilised Criegee intermediate budgets and SO2 oxidation: experiment, theory and modelling

    Directory of Open Access Journals (Sweden)

    M. J. Newland

    2018-05-01

    Full Text Available The gas-phase reaction of alkenes with ozone is known to produce stabilised Criegee intermediates (SCIs. These biradical/zwitterionic species have the potential to act as atmospheric oxidants for trace pollutants such as SO2, enhancing the formation of sulfate aerosol with impacts on air quality and health, radiative transfer and climate. However, the importance of this chemistry is uncertain as a consequence of limited understanding of the abundance and atmospheric fate of SCIs. In this work we apply experimental, theoretical and numerical modelling methods to quantify the atmospheric impacts, abundance and fate of the structurally diverse SCIs derived from the ozonolysis of monoterpenes, the second most abundant group of unsaturated hydrocarbons in the atmosphere. We have investigated the removal of SO2 by SCIs formed from the ozonolysis of three atmospherically important monoterpenes (α-pinene, β-pinene and limonene in the presence of varying amounts of water vapour in large-scale simulation chamber experiments that are representative of boundary layer conditions. The SO2 removal displays a clear dependence on water vapour concentration, but this dependence is not linear across the range of [H2O] explored. At low [H2O] a strong dependence of SO2 removal on [H2O] is observed, while at higher [H2O] this dependence becomes much weaker. This is interpreted as being caused by the production of a variety of structurally (and hence chemically different SCIs in each of the systems studied, which displayed different rates of reaction with water and of unimolecular rearrangement or decomposition. The determined rate constants, k(SCI+H2O, for those SCIs that react primarily with H2O range from 4 to 310  ×  10−15 cm3 s−1. For those SCIs that predominantly react unimolecularly, determined rates range from 130 to 240 s−1. These values are in line with previous results for the (analogous stereo-specific SCI system of syn-/anti-CH3

  9. Enhanced adsorption of acidic gases (CO2, NO2 and SO2) on light metal decorated graphene oxide.

    Science.gov (United States)

    Chen, Chi; Xu, Kui; Ji, Xiao; Miao, Ling; Jiang, Jianjun

    2014-06-14

    The adsorption of several acidic gases (CO2, NO2 and SO2) on light metal (Li, Al) decorated graphene oxide (GO) is theoretically studied, based on the first-principles calculations. Configuration relaxation, binding energy and charge transfer are carried out to discuss the acidic gas adsorption ability of light metal decorated GO. It is found out that Li, Al could be anchored stably by hydroxyl and epoxy groups on GO, and then a strong adsorption of CO2, NO2 and SO2 will occur above these light metals. In contrast to Ti, Li decorated GO exhibits a comparable adsorption ability of acidic gases, but a much smaller interaction with O2 about 2.85-3.98 eV lower in binding energy; and Al decorated GO displays much higher binding energy of all acidic gases with an enhancement of about 0.59-2.29 eV. The results of enhanced acidic gas adsorption ability and a reduced interference by O2 imply that Li, Al decorated GO may be useful and promising for collection and filtration of exhaust gases.

  10. Experimental and simulation studies of iron oxides for geochemical fixation of CO2-SO2 gas mixtures

    Science.gov (United States)

    Garcia, Susana; Rosenbauer, Robert J.; Palandri, James; Maroto-Valer, M. Mercedes

    2011-01-01

    Iron-bearing minerals are reactive phases of the subsurface environment and could potentially trap CO2–SO2gas mixtures derived from fossil fuel combustion processes by their conversion to siderite (FeCO3) and dissolved sulfate. Changes in fluid and mineral compositions resulting from reactions, involving the co-injection of SO2 with CO2 were observed both theoretically and experimentally. Experiments were conducted with a natural hematite (α-Fe2O3) sample. A high pressure-high temperature apparatus was used to simulate conditions in geologic formations deeper than 800 m, where CO2 is in the supercritical state. Solid samples were allowed to react with a NaCl–NaOH brine and SO2-bearing CO2-dominated gas mixtures. The predicted equilibrium mineral assemblage at 100 °C and 250 bar became hematite, dawsonite (NaAl(OH)2CO3), siderite (FeCO3) and quartz (SiO2). Experimentally, siderite and dawsonite, derived from the presence of kaolinite (Al2Si2O5(OH)4) in the parent material, were present in residual solids at longer reaction time intervals, which agreed well with results from the modelling work.

  11. Sulfur-doped graphene via thermal exfoliation of graphite oxide in H2S, SO2, or CS2 gas.

    Science.gov (United States)

    Poh, Hwee Ling; Šimek, Petr; Sofer, Zdeněk; Pumera, Martin

    2013-06-25

    Doping of graphene with heteroatoms is an effective way to tailor its properties. Here we describe a simple and scalable method of doping graphene lattice with sulfur atoms during the thermal exfoliation process of graphite oxides. The graphite oxides were first prepared by Staudenmaier, Hofmann, and Hummers methods followed by treatments in hydrogen sulfide, sulfur dioxide, or carbon disulfide. The doped materials were characterized by scanning electron microscopy, high-resolution X-ray photoelectron spectroscopy, combustible elemental analysis, and Raman spectroscopy. The ζ-potential and conductivity of sulfur-doped graphenes were also investigated in this paper. It was found that the level of doping is more dramatically influenced by the type of graphite oxide used rather than the type of sulfur-containing gas used during exfoliation. Resulting sulfur-doped graphenes act as metal-free electrocatalysts for an oxygen reduction reaction.

  12. One-step flame synthesis of an active Pt/TiO2 catalyst for SO2 oxidation

    DEFF Research Database (Denmark)

    Johannessen, Tue; Koutsopoulos, Sotiris

    2002-01-01

    Flame synthesis as a route for production of composite metal oxides has been employed for the one-step synthesis of a supported noble metal catalyst, i.e. a Pt/TiO2 catalyst, by simultaneous combustion of Ti-isopropoxide and platinum acetylacetonate in a quench-cooled flame reactor. The average...

  13. An overview of emissions of SO2 and NOx and the long-range transport of oxidized sulfur and nitrogen pollutants in East Asia.

    Science.gov (United States)

    Qu, Yu; An, Junling; He, Youjiang; Zheng, Jun

    2016-06-01

    The long-range transport of oxidized sulfur (sulfur dioxide (SO2) and sulfate) and oxidized nitrogen (nitrogen oxides (NOx) and nitrate) in East Asia is an area of increasing scientific interest and political concern. This paper reviews various published papers, including ground- and satellite-based observations and numerical simulations. The aim is to assess the status of the anthropogenic emissions of SO2 and NOx and the long-range transport of oxidized S and N pollutants over source and downwind region. China has dominated the emissions of SO2 and NOx in East Asia and urgently needs to strengthen the control of their emissions, especially NOx emissions. Oxidized S and N pollutants emitted from China are transported to Korea and Japan, due to persistent westerly winds, in winter and spring. However, the total contributions of China to S and N pollutants across Korea and Japan were not found to be dominant over longer time scales (e.g., a year). The source-receptor relationships for oxidized S and N pollutants in East Asia varied widely among the different studies. This is because: (1) the nonlinear effects of atmospheric chemistry and deposition processes were not well considered, when calculating the source-receptor relationships; (2) different meteorological and emission data inputs and solution schemes for key physical and chemical processes were used; and (3) different temporal and spatial scales were employed. Therefore, simulations using the same input fields and similar model configurations would be of benefit, to further evaluate the source-receptor relationships of the oxidized S and N pollutants. Copyright © 2016. Published by Elsevier B.V.

  14. Oxidation of SO2 by stabilized Criegee intermediate (sCI radicals as a crucial source for atmospheric sulfuric acid concentrations

    Directory of Open Access Journals (Sweden)

    M. Boy

    2013-04-01

    Full Text Available The effect of increased reaction rates of stabilized Criegee intermediates (sCIs with SO2 to produce sulfuric acid is investigated using data from two different locations, SMEAR II, Hyytiälä, Finland, and Hohenpeissenberg, Germany. Results from MALTE, a zero-dimensional model, show that using previous values for the rate coefficients of sCI + SO2, the model underestimates gas phase H2SO4 by up to a factor of two when compared to measurements. Using the rate coefficients recently calculated by Mauldin et al. (2012 increases sulfuric acid by 30–40%. Increasing the rate coefficient for formaldehyde oxide (CH2OO with SO2 according to the values recommended by Welz et al. (2012 increases the H2SO4 yield by 3–6%. Taken together, these increases lead to the conclusion that, depending on their concentrations, the reaction of stabilized Criegee intermediates with SO2 could contribute as much as 33–46% to atmospheric sulfuric acid gas phase concentrations at ground level. Using the SMEAR II data, results from SOSA, a one-dimensional model, show that the contribution from sCI reactions to sulfuric acid production is most important in the canopy, where the concentrations of organic compounds are the highest, but can have significant effects on sulfuric acid concentrations up to 100 m. The recent findings that the reaction of sCI + SO2 is much faster than previously thought together with these results show that the inclusion of this new oxidation mechanism could be crucial in regional as well as global models.

  15. Microstructural Investigations of Al2O3 Scale Formed on FeCrAl Steel during High Temperature Oxidation in SO2

    International Nuclear Information System (INIS)

    Homa, M.; Zurek, Z.; Morgiel, B.; Zieba, P.; Wojewoda, J.

    2008-01-01

    The results of microstructure observations of the Al 2 O 3 scale formed on a Fe-Cr-Al steel during high temperature oxidation in the SO 2 atmosphere are presented. Morphology of the scale has been studied by SEM and TEM techniques. Phase and chemical compositions have been studied by EDX and XRD techniques. The alumina oxide is a primary component of the scale. TEM observations showed that the scale was multilayer. The entire surface of the scale is covered with 'whiskers, which look like very thin platelets and have random orientation. The cross section of a sample shows, that the 'whiskers' are approximately 2 μm high, however the compact scale layer on which they reside is 0.2 μm thick. The scale layer was composed mainly of small equiaxial grains and a residual amount of small columnar grains. EDX analysis of the scale surface showed that the any sulfides were found in the formed outer and thin inner scale layer. A phase analysis of the scale formed revealed that it is composed mainly of the θ-Al 2 O 3 phase and a residual amount of α-Al 2 O 3

  16. Effect of relative humidity on O3 and NO2 oxidation of SO2 on α-Al2O3 particles

    Science.gov (United States)

    Liu, Wenjun; He, Xiang; Pang, Shufeng; Zhang, Yunhong

    2017-10-01

    Heterogeneous reactions of SO2/O3 and SO2/NO2 with α-Al2O3 particles at different RHs were investigated using a gas-flow system combined with microscopic Fourier transform infrared (micro-FTIR) spectrometer. The results show that the trace gas O3 or NO2 leads to rapid conversion of SO2 to sulfate on the surface of α-Al2O3 particles in initial stage and then conversion rate decreases in the following stages. The rate of sulfate formation and uptake coefficient (γ) for SO2 in the two systems as a function of relative humidity (RH) are determined for the first time, which are all strongly enhanced more than seven-fold as the RH increase from 15% to 95% in initial stage for SO2/O3 and SO2/NO2. Moreover, the γ in the system of SO2/O3 on α-Al2O3 particles is more than 3-fold than that of SO2/NO2 for the similar RH condition. Our results may be broadly applicable to understand the effects of RH and trace gases (e.g., O3, NO2) for the converting SO2 into sulfate on the mineral dust, which supply basic data for atmospheric chemistry modeling studies.

  17. SO2 - An indirect source of energy

    DEFF Research Database (Denmark)

    Kriek, R.J.; Van Ravenswaay, J.P.; Potgieter, M.

    2013-01-01

    -related processes 12.8 Mt. As a well-known gaseous pollutant, SO2 is not per se known as a source of energy. However, in the presence of water SO2 can be electro-oxidized at the anode of an electrolyser to produce hydrogen ions, which in turn can be reduced at the cathode of the electrolyser to produce hydrogen gas...

  18. Structures and reaction rates of the gaseous oxidation of SO2 by an O− 3 (H2O)0–5 cluster – a density functional theory investigation

    DEFF Research Database (Denmark)

    Bork, Nicolai Christian; Kurten, T.; Enghoff, Martin Andreas Bødker

    2011-01-01

    , the most energetically favorable class of transition states vary with the number of water molecules attached. A kinetic model is utilized, taking into account the most likely outcomes of the initial SO2O3−(H2O)n collision complexes. This model shows that the reaction takes place at collision rates...

  19. O3SO2AI

    Data.gov (United States)

    National Aeronautics and Space Administration — Robust cloud products are critical for DSCOVR to make a significant contribution to climate studies. Building on our team’s track-record in cloud detection, cloud...

  20. The US SO2 Auction

    DEFF Research Database (Denmark)

    Svendsen, Gert Tinggaard; Christensen, Jan Lien

    1998-01-01

    An annual discriminative and revenue-neutral auction is linked to the new Acid Rain Program which allows electric utilities all over the US to trade SO2 emission permits. This innovative SO2 auction distributes 2% of the permits in circulation and takes place at the Chicago Board of Trade. Early...

  1. Effects of H2S on molten carbonate fuel cells. Literature review on the impact of SO2 in the oxidant supplied to molten carbonate fuel cells

    Science.gov (United States)

    Remick, R. J.

    1985-05-01

    The purpose is to identify available information regarding the impact upon fuel cell performance of sulfur dioxide at ppM levels in oxidant gases supplied to molten carbonate fuel cells (MCFC). The general conclusions are as follows: (1) the major source of sulfur dioxide in the oxidant is oxidized sulfur species coming from the fuel; (2) sulfur dioxide in the oxidant can react with oxygen and carbonate to produce sulfate in the electrolyte; (3) sulfate in the electrolyte is Faradaically transported to the anode where it is reduced to hydrogen sulfide; (4) the major and thus far only identifiable mechanism for performance loss in MCFC is caused by this hydrogen sulfide forming nickel sulfide on the anode; and (5) there are a number of other chemical reactions in which sulfur dioxide may participate which have not been investigated. Included in this group are the oxidation to sulfur trioxide and the corrosion of nickel and nickel oxide.

  2. Effect of nitrogen oxides (NO and NO2) and toluene on SO2 photooxidation, nucleation and growth: A smog chamber study

    Science.gov (United States)

    Li, Kangwei; Chen, Linghong; White, Stephen J.; Han, Ke; Lv, Biao; Bao, Kaiji; Wu, Xuecheng; Gao, Xiang; Azzi, Merched; Cen, Kefa

    2017-08-01

    The formation and growth of new particles has recently been shown to have a significant influence on Chinese haze pollution, and sulfuric acid has long been recognized as a major contributor to new particle formation. In this study, four comparison groups of experiments related to SO2 photooxidation, as well as aerosol nucleation and growth, have been conducted in the CAPS-ZJU (Complex Air Pollution Study-Zhejiang University) smog chamber. These were conducted either under SO2/NOx or SO2/toluene gas-phase environments in the absence of seed particles. During aerosol nucleation and growth process, several physical properties such as mass, size and effective density were measured simultaneously by Scanning Mobility Particle Sizer (SMPS) and Differential Mobility Analyzer-Aerosol Particle Mass Analyzer-Condensation Particle Counter (DMA-APM-CPC). The effective density of new particles decreased from 1.8 to 1.35 g/cm3 as the particle size increased from 20 to 65 nm. The single particle mass showed good power-law relationship with mobility diameter, with an average mass-mobility exponent of 2.885. A new algorithm and a reference density of 1.38 g/cm3 based on size-resolved single particle mass (SPM) were proposed to calculate the mass concentration of new particles. Two methods based on Log Normal and Max Concentration were applied to derive particle growth rate (GR), and data merging from both methods was implemented to decrease calculation uncertainty. Meanwhile, both continuous nucleation and inhibition of further growth in sub-20 nm size range were observed in different experiments depending on composition, and possible reasons were analyzed. The presence of NO was found to suppress nucleation and subsequent aerosol growth; while the presence of NO2 or toluene promoted it. It was concluded that decreasing NOx (NO or NO2) or increasing toluene may promote SO2 photooxidation, nucleation and subsequent aerosol growth, all of which is significant for deeper

  3. Fractionation of sulfur isotopes during heterogeneous oxidation of SO2 on sea salt aerosol: a new tool to investigate non-sea salt sulfate production in the marine boundary layer

    Science.gov (United States)

    Harris, E.; Sinha, B.; Hoppe, P.; Foley, S.; Borrmann, S.

    2012-05-01

    The oxidation of SO2 to sulfate on sea salt aerosols in the marine environment is highly important because of its effect on the size distribution of sulfate and the potential for new particle nucleation from H2SO4 (g). However, models of the sulfur cycle are not currently able to account for the complex relationship between particle size, alkalinity, oxidation pathway and rate - which is critical as SO2 oxidation by O3 and Cl catalysis are limited by aerosol alkalinity, whereas oxidation by hypohalous acids and transition metal ions can continue at low pH once alkalinity is titrated. We have measured 34S/32S fractionation factors for SO2 oxidation in sea salt, pure water and NaOCl aerosol, as well as the pH dependency of fractionation. Oxidation of SO2 by NaOCl aerosol was extremely efficient, with a reactive uptake coefficient of ≈0.5, and produced sulfate that was enriched in 32S with αOCl = 0.9882±0.0036 at 19 °C. Oxidation on sea salt aerosol was much less efficient than on NaOCl aerosol, suggesting alkalinity was already exhausted on the short timescale of the experiments. Measurements at pH = 2.1 and 7.2 were used to calculate fractionation factors for each step from SO2(g) → multiple steps → SOOCl2-. Oxidation on sea salt aerosol resulted in a lower fractionation factor than expected for oxidation of SO32- by O3 (αseasalt = 1.0124±0.0017 at 19 °C). Comparison of the lower fractionation during oxidation on sea salt aerosol to the fractionation factor for high pH oxidation shows HOCl contributed 29% of S(IV) oxidation on sea salt in the short experimental timescale, highlighting the potential importance of hypohalous acids in the marine environment. The sulfur isotope fractionation factors measured in this study allow differentiation between the alkalinity-limited pathways - oxidation by O3 and by Cl catalysis (α34 = 1.0163±0.0018 at 19 °C in pure water or 1.0199±0.0024 at pH = 7.2) - which favour the heavy isotope, and the alkalinity non

  4. Fractionation of sulfur isotopes during heterogeneous oxidation of SO2 on sea salt aerosol: a new tool to investigate non-sea salt sulfate production in the marine boundary layer

    Directory of Open Access Journals (Sweden)

    S. Borrmann

    2012-05-01

    Full Text Available The oxidation of SO2 to sulfate on sea salt aerosols in the marine environment is highly important because of its effect on the size distribution of sulfate and the potential for new particle nucleation from H2SO4 (g. However, models of the sulfur cycle are not currently able to account for the complex relationship between particle size, alkalinity, oxidation pathway and rate – which is critical as SO2 oxidation by O3 and Cl catalysis are limited by aerosol alkalinity, whereas oxidation by hypohalous acids and transition metal ions can continue at low pH once alkalinity is titrated. We have measured 34S/32S fractionation factors for SO2 oxidation in sea salt, pure water and NaOCl aerosol, as well as the pH dependency of fractionation. Oxidation of SO2 by NaOCl aerosol was extremely efficient, with a reactive uptake coefficient of ≈0.5, and produced sulfate that was enriched in 32S with αOCl = 0.9882±0.0036 at 19 °C. Oxidation on sea salt aerosol was much less efficient than on NaOCl aerosol, suggesting alkalinity was already exhausted on the short timescale of the experiments. Measurements at pH = 2.1 and 7.2 were used to calculate fractionation factors for each step from SO2(g → multiple steps → SOOCl2−. Oxidation on sea salt aerosol resulted in a lower fractionation factor than expected for oxidation of SO32− by O3 (αseasalt = 1.0124±0.0017 at 19 °C. Comparison of the lower fractionation during oxidation on sea salt aerosol to the fractionation factor for high pH oxidation shows HOCl contributed 29% of S(IV oxidation on sea salt in the short experimental timescale, highlighting the potential importance of hypohalous acids in the marine environment. The sulfur isotope fractionation factors measured in this study allow differentiation between the alkalinity-limited pathways – oxidation by O3 and by Cl catalysis (α34 = 1.0163±0.0018 at 19 °C in pure water or 1.0199±0.0024 at pH = 7.2 – which favour the heavy isotope, and

  5. Diagnosis of deactivation sources for vanadium catalysts used in SO 2 oxidation reaction and optimization of vanadium extraction from deactivated catalysts

    Science.gov (United States)

    Ksibi, Mohamed; Elaloui, Elimam; Houas, Ammar; Moussa, Noomen

    2003-12-01

    Physico-chemical analysis (X-ray, FTIR) and/or methanol oxidation reaction test were performed on fresh and deactivated vanadium catalysts used in H 2SO 4 manufacturing. It allowed the diagnosis of catalyst deactivation sources, as well as the processes of regenerating and recycling the worn out catalyst in converter. One of these processes is hydrometallurgical method. It consists in treating the deactivated catalyst with alkaline or acidic reagents and forming vanadate solution. A simple and non-costly operation of chemical attack permits the extraction of vanadium from silica in deactivated catalyst. The extracted vanadium can be used for the confection of regenerated catalysts or metallic tools. After optimization, this method can be used for industrial application.

  6. Aqueous phase oxidation of sulphur dioxide by ozone in cloud droplets

    Science.gov (United States)

    Hoyle, C. R.; Fuchs, C.; Järvinen, E.; Saathoff, H.; Dias, A.; El Haddad, I.; Gysel, M.; Coburn, S. C.; Tröstl, J.; Bernhammer, A.-K.; Bianchi, F.; Breitenlechner, M.; Corbin, J. C.; Craven, J.; Donahue, N. M.; Duplissy, J.; Ehrhart, S.; Frege, C.; Gordon, H.; Höppel, N.; Heinritzi, M.; Kristensen, T. B.; Molteni, U.; Nichman, L.; Pinterich, T.; Prévôt, A. S. H.; Simon, M.; Slowik, J. G.; Steiner, G.; Tomé, A.; Vogel, A. L.; Volkamer, R.; Wagner, A. C.; Wagner, R.; Wexler, A. S.; Williamson, C.; Winkler, P. M.; Yan, C.; Amorim, A.; Dommen, J.; Curtius, J.; Gallagher, M. W.; Flagan, R. C.; Hansel, A.; Kirkby, J.; Kulmala, M.; Möhler, O.; Stratmann, F.; Worsnop, D. R.; Baltensperger, U.

    2016-02-01

    The growth of aerosol due to the aqueous phase oxidation of sulfur dioxide by ozone was measured in laboratory-generated clouds created in the Cosmics Leaving OUtdoor Droplets (CLOUD) chamber at the European Organization for Nuclear Research (CERN). Experiments were performed at 10 and -10 °C, on acidic (sulfuric acid) and on partially to fully neutralised (ammonium sulfate) seed aerosol. Clouds were generated by performing an adiabatic expansion - pressurising the chamber to 220 hPa above atmospheric pressure, and then rapidly releasing the excess pressure, resulting in a cooling, condensation of water on the aerosol and a cloud lifetime of approximately 6 min. A model was developed to compare the observed aerosol growth with that predicted using oxidation rate constants previously measured in bulk solutions. The model captured the measured aerosol growth very well for experiments performed at 10 and -10 °C, indicating that, in contrast to some previous studies, the oxidation rates of SO2 in a dispersed aqueous system can be well represented by using accepted rate constants, based on bulk measurements. To the best of our knowledge, these are the first laboratory-based measurements of aqueous phase oxidation in a dispersed, super-cooled population of droplets. The measurements are therefore important in confirming that the extrapolation of currently accepted reaction rate constants to temperatures below 0 °C is correct.

  7. Aqueous phase oxidation of sulphur dioxide by ozone in cloud droplets

    Directory of Open Access Journals (Sweden)

    C. R. Hoyle

    2016-02-01

    Full Text Available The growth of aerosol due to the aqueous phase oxidation of sulfur dioxide by ozone was measured in laboratory-generated clouds created in the Cosmics Leaving OUtdoor Droplets (CLOUD chamber at the European Organization for Nuclear Research (CERN. Experiments were performed at 10 and −10 °C, on acidic (sulfuric acid and on partially to fully neutralised (ammonium sulfate seed aerosol. Clouds were generated by performing an adiabatic expansion – pressurising the chamber to 220 hPa above atmospheric pressure, and then rapidly releasing the excess pressure, resulting in a cooling, condensation of water on the aerosol and a cloud lifetime of approximately 6 min. A model was developed to compare the observed aerosol growth with that predicted using oxidation rate constants previously measured in bulk solutions. The model captured the measured aerosol growth very well for experiments performed at 10 and −10 °C, indicating that, in contrast to some previous studies, the oxidation rates of SO2 in a dispersed aqueous system can be well represented by using accepted rate constants, based on bulk measurements. To the best of our knowledge, these are the first laboratory-based measurements of aqueous phase oxidation in a dispersed, super-cooled population of droplets. The measurements are therefore important in confirming that the extrapolation of currently accepted reaction rate constants to temperatures below 0 °C is correct.

  8. submitter Aqueous phase oxidation of sulphur dioxide by ozone in cloud droplets

    CERN Document Server

    Hoyle, C R; Järvinen, E; Saathoff, H; Dias, A; El Haddad, I; Gysel, M; Coburn, S C; Tröstl, J; Bernhammer, A -K; Bianchi, F; Breitenlechner, M; Corbin, J C; Craven, J; Donahue, N M; Duplissy, J; Ehrhart, S; Frege, C; Gordon, H; Höppel, N; Heinritzi, M; Kristensen, T B; Molteni, U; Nichman, L; Pinterich, T; Prévôt, A S H; Simon, M; Slowik, J G; Steiner, G; Tomé, A; Vogel, A L; Volkamer, R; Wagner, A C; Wagner, R; Wexler, A S; Williamson, C; Winkler, P M; Yan, C; Amorim, A; Dommen, J; Curtius, J; Gallagher, M W; Flagan, R C; Hansel, A; Kirkby, J; Kulmala, M; Möhler, O; Stratmann, F; Worsnop, D R; Baltensperger, U

    2016-01-01

    The growth of aerosol due to the aqueous phase oxidation of sulfur dioxide by ozone was measured in laboratory-generated clouds created in the Cosmics Leaving OUtdoor Droplets (CLOUD) chamber at the European Organization for Nuclear Research (CERN). Experiments were performed at 10 and −10 °C, on acidic (sulfuric acid) and on partially to fully neutralised (ammonium sulfate) seed aerosol. Clouds were generated by performing an adiabatic expansion – pressurising the chamber to 220 hPa above atmospheric pressure, and then rapidly releasing the excess pressure, resulting in a cooling, condensation of water on the aerosol and a cloud lifetime of approximately 6 min. A model was developed to compare the observed aerosol growth with that predicted using oxidation rate constants previously measured in bulk solutions. The model captured the measured aerosol growth very well for experiments performed at 10 and −10 °C, indicating that, in contrast to some previous studies, the oxidation rates of SO2 in ...

  9. Mechanisms of radical removal by SO2

    DEFF Research Database (Denmark)

    Rasmussen, Christian Lund; Glarborg, Peter; Marshall, Paul

    2007-01-01

    It is well established from experiments in premixed, laminar flames, jet-stirred reactors, flow reactors, and batch reactors that SO2 acts to catalyze hydrogen atom removal at stoichiometric and reducing conditions. However, the commonly accepted mechanism for radical removal, SO2 + H(+M) reversi......It is well established from experiments in premixed, laminar flames, jet-stirred reactors, flow reactors, and batch reactors that SO2 acts to catalyze hydrogen atom removal at stoichiometric and reducing conditions. However, the commonly accepted mechanism for radical removal, SO2 + H...

  10. Emission of SO2 from Cement Production

    DEFF Research Database (Denmark)

    Hu, Guilin

    2007-01-01

    Ph. D. afhandlingen omhandler problemstillinger af speciel relevans for cementproduktion med lave emissioner af svolvdioxid. Afhandlingen omfatter dels pyritoxidation – dvs. dannelse af SO2, dels direkte sulfatering af kalksten – dvs. absorptionen af SO2 på CaCO3 under oxiderende betingelser i te...

  11. Implementing SO2 Emissions in China

    International Nuclear Information System (INIS)

    Schreifels, J.; Yang, J.

    2003-01-01

    Over the past 10 years, the Chinese State Environmental Protection Administration (SEPA) has actively investigated the potential to use emission trading to reduce sulphur dioxide (SO2) emissions from electricity generators and industrial sources. In 1999, SEPA partnered with the U.S. Environmental Protection Agency (U.S. EPA) to cooperate on a study to assess the feasibility of implementing SO2 emission trading in China. SEPA has also pursued emission trading pilot projects in several cities and provinces. The authors, using information from the feasibility study and pilot projects, introduce the circumstances necessary for SO2 emission trading in China, outline the experience to date, and analyse implementation opportunities and barriers in China. The contents of the paper are: (1) SO2 emission control policies in China; (2) institutional requirements and the basis for introducing SO2 emission trading in China; (3) case studies of emission trading in China; (4) opportunities and barriers to implementing emission trading in China; (5) recommendations to transition from pilot projects to a nationwide SO2 emission trading program; and (6) conclusions and suggestions

  12. Potential Impact of Microbial Activity on the Oxidant Capacity and the Organic Carbon Budget in Clouds (Invited)

    Science.gov (United States)

    Delort, A.

    2013-12-01

    Within cloud water, microorganisms are metabolically active; so they are suspected to contribute to atmospheric chemistry. This paper is focused on the interactions between microorganisms and Reactive Oxygenated Species present in cloud water since these chemical compounds are driving the oxidant capacity of the cloud system. For this, real cloud waters with contrasting features (marine, continental, urban) were sampled at the puy de Dôme mountain (France). They exhibit high microbial biodiversity and complex chemical composition. These media were incubated in the dark and subjected to UV-light radiation in specifically designed photo-bio-reactors. The concentrations of hydrogen peroxide (H2O2), organic compounds and the ATP/ADP ratio were monitored during the incubation period. Microorganisms remained metabolically active in the presence of hydroxyl radicals photo-produced from H2O2. This oxidant and major carbon compounds (formaldehyde and carboxylic acids) were biodegraded by the endogenous microflora. This work suggests that microorganisms could play a double role in atmospheric chemistry: first, they could directly metabolize organic carbon species; second they could reduce the available source of radicals due to their oxidative metabolism. Consequently, molecules such as H2O2 would be no longer available for photochemical or other chemical reactions, decreasing the cloud oxidant capacity.

  13. Imaging volcanic CO2 and SO2

    Science.gov (United States)

    Gabrieli, A.; Wright, R.; Lucey, P. G.; Porter, J. N.

    2017-12-01

    Detecting and quantifying volcanic carbon dioxide (CO2) and sulfur dioxide (SO2) emissions is of relevance to volcanologists. Changes in the amount and composition of gases that volcanoes emit are related to subsurface magma movements and the probability of eruptions. Volcanic gases and related acidic aerosols are also an important atmospheric pollution source that create environmental health hazards for people, animals, plants, and infrastructures. For these reasons, it is important to measure emissions from volcanic plumes during both day and night. We present image measurements of the volcanic plume at Kīlauea volcano, HI, and flux derivation, using a newly developed 8-14 um hyperspectral imaging spectrometer, the Thermal Hyperspectral Imager (THI). THI is capable of acquiring images of the scene it views from which spectra can be derived from each pixel. Each spectrum contains 50 wavelength samples between 8 and 14 um where CO2 and SO2 volcanic gases have diagnostic absorption/emission features respectively at 8.6 and 14 um. Plume radiance measurements were carried out both during the day and the night by using both the lava lake in the Halema'uma'u crater as a hot source and the sky as a cold background to detect respectively the spectral signatures of volcanic CO2 and SO2 gases. CO2 and SO2 path-concentrations were then obtained from the spectral radiance measurements using a new Partial Least Squares Regression (PLSR)-based inversion algorithm, which was developed as part of this project. Volcanic emission fluxes were determined by combining the path measurements with wind observations, derived directly from the images. Several hours long time-series of volcanic emission fluxes will be presented and the SO2 conversion rates into aerosols will be discussed. The new imaging and inversion technique, discussed here, are novel allowing for continuous CO2 and SO2 plume mapping during both day and night.

  14. Sulfation of Condensed Potassium Chloride by SO2

    DEFF Research Database (Denmark)

    Sengeløv, Louise With; Hansen, Troels Bruun; Bartolomé, Carmen

    2013-01-01

    The interaction between alkali chloride and sulfur oxides has important implications for deposition and corrosion in combustion of biomass. In the present study, the sulfation of particulate KCl (90–125 μm) by SO2 was studied in a fixed bed reactor in the temperature range 673–1023 K and with rea......The interaction between alkali chloride and sulfur oxides has important implications for deposition and corrosion in combustion of biomass. In the present study, the sulfation of particulate KCl (90–125 μm) by SO2 was studied in a fixed bed reactor in the temperature range 673–1023 K...... and with reactant concentrations of 500–3000 ppm SO2, 1–20% O2, and 4–15% H2O. The degree of sulfation was monitored by measuring the formation of HCl. Analysis of the solid residue confirmed that the reaction proceeds according to a shrinking core model and showed the formation of an eutectic at higher...... temperatures. On the basis of the experimental results, a rate expression for the sulfation reaction was derived. The model compared well with literature data for sulfation of KCl and NaCl, and the results indicate that it may be applied at even higher SO2 concentrations and temperatures than those...

  15. Modeling of 2008 Kasatochi Volcanic Sulfate Direct Radiative Forcing: Assimilation of OMI SO2 Plume Height Data and Comparison with MODIS and CALIOP Observations

    Science.gov (United States)

    Wang, J.; Park, S.; Zeng, J.; Ge, C.; Yang, K.; Carn, S.; Krotkov, N.; Omar, A. H.

    2013-01-01

    Volcanic SO2 column amount and injection height retrieved from the Ozone Monitoring Instrument (OMI) with the Extended Iterative Spectral Fitting (EISF) technique are used to initialize a global chemistry transport model (GEOS-Chem) to simulate the atmospheric transport and lifecycle of volcanic SO2 and sulfate aerosol from the 2008 Kasatochi eruption, and to subsequently estimate the direct shortwave, top-of-the-atmosphere radiative forcing of the volcanic sulfate aerosol. Analysis shows that the integrated use of OMI SO2 plume height in GEOS-Chem yields: (a) good agreement of the temporal evolution of 3-D volcanic sulfate distributions between model simulations and satellite observations from the Moderate Resolution Imaging Spectroradiometer (MODIS) and Cloud-Aerosol Lidar with Orthogonal Polarisation (CALIOP), and (b) an e-folding time for volcanic SO2 that is consistent with OMI measurements, reflecting SO2 oxidation in the upper troposphere and stratosphere is reliably represented in the model. However, a consistent (approx. 25 %) low bias is found in the GEOS-Chem simulated SO2 burden, and is likely due to a high (approx.20 %) bias of cloud liquid water amount (as compared to the MODIS cloud product) and the resultant stronger SO2 oxidation in the GEOS meteorological data during the first week after eruption when part of SO2 underwent aqueous-phase oxidation in clouds. Radiative transfer calculations show that the forcing by Kasatochi volcanic sulfate aerosol becomes negligible 6 months after the eruption, but its global average over the first month is -1.3W/sq m, with the majority of the forcing-influenced region located north of 20degN, and with daily peak values up to -2W/sq m on days 16-17. Sensitivity experiments show that every 2 km decrease of SO2 injection height in the GEOS-Chem simulations will result in a approx.25% decrease in volcanic sulfate forcing; similar sensitivity but opposite sign also holds for a 0.03 m increase of geometric radius of

  16. Hard target LIDAR calibration for SO2

    CSIR Research Space (South Africa)

    Du Plessis, A

    2006-01-01

    Full Text Available -R-MAP hardware: laser system • Tunable Alexandrite: • Fundamental @ 750 nm • 2nd Harmonic @ 375 nm • 3rd Harmonic @ 250 nm • Hydrogen Raman cell @ 75 bar • Raman-shifted 3rd harmonic @ 280 nm Slide 12 © CSIR 2006 www....csir.co.za Choice of wavelength 220 240 260 280 300 320 340 360 380 400 420 440 0 1 2 3 4 5 6 7 8 9 10 11 12 13 Raman shifted 3rd harmonic3nd Harmonic 2nd Harmonic NO2 SO2 A b s o r p t i o n c r o s s - s e c t i o n...

  17. Electron beam process for SO2 removal from flue gases with high SO2 content

    International Nuclear Information System (INIS)

    Licki, J.; Chmielewski, A.G.; Zimek, Z.; Tyminski, B.; Bulka, S.

    2002-01-01

    Flue gases with high SO 2 concentration are emitted from different industrial processes, e.g. combustion of coal with high sulfur content, copper smelting and sintering plant. The application of the electron beam process for SO 2 removal from such flue gases was investigated. A parametric study was carried out to determine the removal efficiency as a function of temperature and humidity of irradiated gases, dose and ammonia stoichiometry. At the dose 11.5 kGy 95% SO 2 removal efficiency was obtained when the temperature and humidity of irradiated flue gases and ammonia stoichiometry were properly adjusted. The synergistic effect of high SO 2 concentration on NO x removal was observed. The collected by-product was the mixture of (NH 4 ) 2 SO 4 and NH 4 NO 3 . The content of heavy metals in the by-product was many times lower than the values acceptable for commercial fertilizer

  18. The oxidation of SO2 by NO2(g) at the air-water interface of aquated aerosol: implications for the rapid onset of haze-aerosol events in China

    Science.gov (United States)

    Li, L.; Colussi, A. J.; Hoffmann, M. R.

    2017-12-01

    Aqueous phase chemistry plays a vital role in the global atmosphere. The importance of heterogeneous chemistry has been recently underscored by the severe haze-fog pollution episodes experienced in Chinese megacities. A key finding is that despite reduced photochemistry during the wintertime haze events, the oxidation of S(IV) into sulfate aerosol occurs rapidly in spite of the low levels of ozone and H2O2. Field observations suggest that NO2 could serve as a suitable oxidant of S(IV) during the events under neutral pH conditions. However, the haze aerosols are mostly acidic. Furthermore, the air-water interface is more acidic than bulk-phase aquated system according to our recent findings. This work investigates the chemistry taking place as NO2(g) collides with the surface of aqueous S(IV) microdroplets as a function of pH to closely simulate actual haze aerosol events under atmospheric conditions. The reaction between NO2(g) and HSO3- (aq) is studied in situ under ambient temperature and pressure via online electrospray ionization mass spectrometry. The aqueous aerosols containing HSO3- is generated using a microjet which is exposed to NO2(g) alternatively, while the composition of the 1 nm interfacial liquid layer of the aerosol is instantaneously measured. The ratio of HSO3- to HSO4- is observed to decrease with the concomitant appearance of a strong m/z 62 signal upon NO2(g) exposure. The appearance of m/z 62 indicates the formation of NO3- via the disproportionation of NO2 (2NO2(g) + H2O (l) ⇌ H++NO3-(aq) + HONO(aq)) and thus impacts the ion-ion interactions of NO3- on the ratio of HSO3- to HSO4- in the outermost interfacial layers. Parallel experiments with NO3-(aq) additions are conducted to quantify the impact of NO3- on the the ratio, in order to unravel the contribution of NO2 to the oxidation of S(IV). After accounting for the HNO3 effect, it is concluded: (1) most NO2(g) is converted into NO3- via anion-catalyzed hydrolytic disproportionation; (2

  19. Measurements of 32SO2, 33SO2, 34SO2 and 36SO2 high-resolution cross-sections and isotope effects by SO2 self-shielding

    Science.gov (United States)

    Endo, Y.; Ogawa, M.; Danielache, S. O.; Ueno, Y.

    2017-12-01

    Archean sulfur mass-independent fractionation (S-MIF) is a unique proxy within the geological and geochemical records for studying the composition of the Archean atmosphere. S-MIF signatures are defined as Δ33S = δ33S - 0.515×δ34S and Δ36S = δ36S - 1.90×δ34S. Archean S-MIF is characterized as Δ36S/Δ33S = -1. Recent SO2 photochemical experiments under specific reducing conditions reproduced the Archean trend for the first time [1]. Self-shielding of SO2 photolysis and intersystem crossing in excited SO2 are probably key mechanisms for explaining Archean S-MIF. Self-shielding is originated from UV spectra changed by upper SO2 own absorption. Because 32S accounts for about 95% of all sulfur isotopes, the photolysis rate constant of only 32SO2 is lower than other isotopologue. Thus, SO2 photolysis in the bottom of the atmosphere undergoes mass-independent fractionation. Fractionation factors by SO2 photolysis reaction can be calculated by absorption cross-sections of 32SO2, 33SO2, 34SO2 and 36SO2 and respective quantum yields. Quantitative estimations self-shielding fractionation factors requires high-spectral resolution cross-sections, but they have not been reported yet. Here we report measurements of high-resolution cross-sections (1cm-1) and fractionation factors by SO2 photolysis including self-shielding. Moreover, because the absorption wavelength varies with each isotopologue, photolysis rate constants of all isotopologues (32S16O2, 32S16O18O, etc) should be different. Then self-shielding may affect the ratio of isotopologues such as clumped-isotopes. We calculated preliminary calculation clumped isotope enrichment in residual species by self-shielding. Reference: [1] Endo, Y., Ueno, Y., Aoyama, S., & Danielache, S. O. (2016). Sulfur isotope fractionation by broadband UV radiation to optically thin SO2 under reducing atmosphere. EPSL, 453, 9-22.

  20. The US SO2 allowance trading program

    International Nuclear Information System (INIS)

    Ellerman, A.D.

    2001-01-01

    The US SO 2 Allowance Trading Program is the world's first large-scale application of a cap-and-trade mechanism for limiting emissions, and it is often cited as an example for the control of other pollutants and of greenhouse gases. Drawing upon experience with this novel approach to omissions control since 1995, this article makes five observations that address common misunderstandings about emissions trading and that are applicable to the control of greenhouse gases. First, emissions trading did not compromise environmental effectiveness, and even enhanced it. Second, the program works because of the simplicity of the compliance requirement, the unavoidably strict accountability of the system, and the complete flexibility given to emitting sources. All three go together to form what may be regarded as a virtuous circle. Third, despite fears to the contrary, allowance markets developed in response to trading opportunities. Fourth, the politics of allowance allocation can be helpful in overcoming objections to emission control measures. Finally, provisions for voluntary accession present problems of moral hazard that must be carefully considered. (author)

  1. CF3SO2X (X = Na, Cl as reagents for trifluoromethylation, trifluoromethylsulfenyl-, -sulfinyl- and -sulfonylation and chlorination. Part 2: Use of CF3SO2Cl

    Directory of Open Access Journals (Sweden)

    Hélène Chachignon

    2017-12-01

    Full Text Available The recent progresses of the application of trifluoromethanesulfonyl chloride, CF3SO2Cl, in the formation of C–CF3, C–SCF3, C–SOCF3, and C–Cl bonds are summarised in this second part of a two-part review published back-to-back on both sodium trifluoromethanesulfinate, CF3SO2Na, (Part 1 and trifluoromethanesulfonyl chloride, CF3SO2Cl (Part 2. There are many reactions in common between these two reagents but it should be noted that CF3SO2Cl reacts under reductive conditions while CF3SO2Na requires oxidative conditions. Electrophilic chlorination is obviously the exclusive preserve of CF3SO2Cl that has been exploited with emphasis in enantioselective chlorination.

  2. Soil acidification in China: is controlling SO2 emissions enough?

    Science.gov (United States)

    Zhao, Yu; Duan, Lei; Xing, Jia; Larssen, Thorjorn; Nielsen, Chris P; Hao, Jiming

    2009-11-01

    Facing challenges of increased energy consumption and related regional air pollution, China has been aggressively implementing flue gas desulfurization (FGD) and phasing out small inefficient units in the power sector in order to achieve the national goal of 10% reduction in sulfur dioxide (SO(2)) emissions from 2005 to 2010. In this paper, the effect of these measures on soil acidification is explored. An integrated methodology is used, combining emission inventory data, emission forecasts, air quality modeling, and ecological sensitivities indicated by critical load. National emissions of SO(2), oxides of nitrogen (NO(X)), particulate matter (PM), and ammonia (NH(3)) in 2005 were estimated to be 30.7, 19.6, 31.3, and 16.6 Mt, respectively. Implementation of existing policy will lead to reductions in SO(2) and PM emissions, while those of NO(X) and NH(3) will continue to rise, even under tentatively proposed control measures. In 2005, the critical load for soil acidification caused by sulfur (S) deposition was exceeded in 28% of the country's territory, mainly in eastern and south-central China. The area in exceedance will decrease to 26% and 20% in 2010 and 2020, respectively, given implementation of current plans for emission reductions. However, the exceedance of the critical load for nitrogen (N, combining effects of eutrophication and acidification) will double from 2005 to 2020 due to increased NO(X) and NH(3) emissions. Combining the acidification effects of S and N, the benefits of SO(2) reductions during 2005-2010 will almost be negated by increased N emissions. Therefore abatement of N emissions (NO(X) and NH(3)) and deposition will be a major challenge to China, requiring policy development and technology investments. To mitigate acidification in the future, China needs a multipollutant control strategy that integrates measures to reduce S, N, and PM.

  3. Electrochemical waste clean-up process for simultaneous removal of SO2 and NOx

    International Nuclear Information System (INIS)

    Juettner, K.; Kreysa, G.; Kleifges, K.H.; Rottmann, R.

    1994-01-01

    Based on the principles of electrochemical exhaust purification, a new process for electrochemical simultaneous removal of SO 2 and NO x is presented. It combines an ''cruter call'' process for NO x reduction with dithionite as homogeneous redox mediator with an ''inner cell'' process for direct oxidation of SO 2 in the anodic space of an electrochemical cell. Absorption experiments for NO x and SO 2 were carried out in separate laboratory scale electrochemical cells. Results are presented. (orig./BBR) [de

  4. Measuring the complex behavior of the SO2 oxidation reaction

    Directory of Open Access Journals (Sweden)

    Muhammad Shahzad

    2015-09-01

    Full Text Available The two step reversible chemical reaction involving five chemical species is investigated. The quasi equilibrium manifold (QEM and spectral quasi equilibrium manifold (SQEM are used for initial approximation to simplify the mechanisms, which we want to utilize in order to investigate the behavior of the desired species. They show a meaningful picture, but for maximum clarity, the investigation method of invariant grid (MIG is employed. These methods simplify the complex chemical kinetics and deduce low dimensional manifold (LDM from the high dimensional mechanism. The coverage of the species near equilibrium point is investigated and then we shall discuss moving along the equilibrium of ODEs. The steady state behavior is observed and the Lyapunov function is utilized to study the stability of ODEs. Graphical results are used to describe the physical aspects of measurements.

  5. Attribution of modeled atmospheric sulfate and SO2 in the Northern Hemisphere for June–July 1997

    Directory of Open Access Journals (Sweden)

    C. M. Benkovitz

    2006-01-01

    Full Text Available Anthropogenic sulfate aerosol is a major contributor to shortwave radiative forcing of climate change by direct light scattering and by perturbing cloud properties and to local concentrations of atmospheric particulate matter. Here we analyze results from previously published calculations with an Eulerian transport model for atmospheric sulfur species in the Northern Hemisphere in June–July, 1997 to quantify the absolute and relative contributions of specific source regions (North America, Europe, and Asia and SO2-to-sulfate conversion mechanisms (gas-phase, aqueous-phase and primary sulfate to sulfate and SO2 column burdens as a function of location and time. Although material emitted within a given region dominates the sulfate and SO2 column burden in that region, examination of time series at specific locations shows that material imported from outside can make a substantial and occasionally dominant contribution. Frequently the major fraction of these exogenous contributions to the sulfate column burden was present aloft, thus minimally impacting air quality at the surface, but contributing substantially to the burden and, by implication, to radiative forcing and diminution of surface irradiance. Although the dominant sulfate formation pathway in the domain as a whole is aqueous-phase reaction in clouds (62%, in regions with minimum opportunity for aqueous-phase reaction gas-phase oxidation is dominant, albeit with considerable temporal variability depending on meteorological conditions. These calculations highlight the importance of transoceanic transport of sulfate, especially at the western margins of continents under the influence of predominantly westerly transport winds.

  6. Physiological characteristics of Plantago major under SO2exposure as affected by foliar iron spray.

    Science.gov (United States)

    Mohasseli, Vahid; Khoshgoftarmanesh, Amir Hossein; Shariatmadari, Hossein

    2017-08-01

    Sulfur dioxide (SO 2 ) is considered as a main air pollutant in industrialized areas that can damage vegetation. In the present study, we investigated how exposure to SO 2 and foliar application of iron (Fe) would affect certain physiological characteristics of Plantago major. The plant seedlings exposed or unexposed to SO 2 (3900 μg m -3 ) were non-supplemented or supplemented with Fe (3 g L -1 ) as foliar spray. Plants were exposed to SO 2 for 6 weeks in 100 × 70 × 70 cm chambers. Fumigation of plants with SO 2 was performed for 3 h daily for 3 days per week (alternate day). Lower leaf Fe concentration in the plants exposed to SO 2 at no added Fe treatment was accompanied with incidence of chlorosis symptoms and reduced chlorophyll concentration. No visible chlorotic symptoms were observed on the SO 2 -exposed plants supplied with Fe that accumulated higher Fe in their leaves. Both at with and without added Fe treatments, catalase (CAT) and peroxidase (POD) activity was higher in the plants fumigated with SO 2 in comparison with those non-fumigated with SO 2 . Foliar application of Fe was also effective in increasing activity of antioxidant enzymes CAT and POD. Exposure to SO 2 led to reduced cellulose but enhanced lignin content of plant leaf cell wall. The results obtained showed that foliar application of Fe was effective in reducing the effects of exposure to SO 2 on cell wall composition. In contrast to SO 2 , application of Fe increased cellulose while decreased lignin content of the leaf cell wall. This might be due to reduced oxidative stress induced by SO 2 in plants supplied with Fe compared with those unsupplied with Fe.

  7. EFFECTS OF FLY ASH TRANSITION METAL CONTENT AND FLUE GAS HCL/SO2 RATIO ON MERCURY SPECIATION IN WASTE COMBUSTION

    Science.gov (United States)

    The paper presents results of research on the effect of sulfur dioxide (SO2):HCI ratio on heterogeneous Hg0 oxidation. The addition of SO2 to moist flue gas at high SO2:HCI ratios (4:1 to 10:1) caused a decrease in oxidation of Hg0 relative to flur gas without SO2. This is attrib...

  8. Multiple sulfur isotope determination on SO2 gas

    Science.gov (United States)

    Halas, Stanislaw; Pienkos, Tomasz

    2017-04-01

    The principal motivation of this study is to apply SO2 gas in the multiple isotope analysis (i.e. simultaneous analysis of sulfur isotope ratios: 33S/32S , 34S/32S and 36S/32S) rather than SF6 gas. SO2 gas can be easily prepared from sulfides (Robinson and Kusakabe 1975) and from sulfates (Halas and Wolacewicz 1981), whilst the preparation of SF6 gas requires the use of a fluorination line (Ono et al. 2006) and a mass spectrometer with enhanced resolving power to resolve isotope peaks 33SF5- from 32SF5- (masses 128 and 127). In the patent application (Halas et al. 2016) we have described a new ion source which can be applied for analysis of gases. The new ion source significantly enhances generation, both positive and negative, ions in comparison to commonly used Nier type. The analyzed gas is admitted from a dual inlet system to the ion source through separate capillaries connected to the pneumatically operated changeover valve as described by Halas (1979). It is important to have SO2 samples well purified from volatiles which eliminates O2 interference at mass 32 peak. A great advantage of the isotope analysis on S+ instead on SO+ or SO2+spectra is that there is no need to keep constant oxygen isotopic composition in the SO2 gas. Usually sulfide and sulfate samples have different oxygen, but it doesn't matter in the case of analysis on S+. The achieved precision (1σ) on positive ion beams was better than 0.1‰ and 0.01‰ for δ36S and δ34S, respectively. Unfortunately δ33S cannot be measured in this way, because of formation of 32SH+ ions which interfere with 33S+. The details of the design of the ion source, vacuum system and electronic controllers are presented in the poster. We thank to Dr. Keith Hackley for donation of an old mass spectrometer to UMCS, on the basis of which we were able to develop the new instrument. This study was supported by NCN project 2013/11/B/ST10/00250. References Hałas S., Pieńkos T., Pelc A., Wójtowicz A. (2016) Patent

  9. Mt. Pinatubo SO2 Column Measurements From Mauna Loa

    Science.gov (United States)

    Goldman, A.; Murcray, F. J.; Rinsland, C. P.; Blatherwick, R. D.; David, S. J.; Murcray, F. H.; Murcray, D. G.

    1992-01-01

    Absorption features of the nu(sub 1) band of SO2 have been identified in high resolution infrared solar absorption spectra recorded from Mauna Loa, Hawaii, on July 9 and 12, 1991, shortly after the arrival of the first eruption plume from the Mt. Pinatubo volcano in the Phillipines. A total SO2 vertical column amount of (5.1 +/- 0.5) x 10(exp 16) molecules/sq cm on July 9 has been retrieved based on nonlinear least- squares spectral fittings of 9 selected SO2 absorption features with an updated set of SO2 spectral parameters. A SO2 total column upper limit of 0.9 x 10(esp 16) molecules/sq cm deduced from measurements on September 20-24, 1991, is consistent with the dispersion of the SO2 cloud and the rapid conversion of the SO2 vapor into volcanic aerosol particles.

  10. Future prices and market for SO2 allowances

    International Nuclear Information System (INIS)

    Sanghi, A.; Joseph, A.; Michael, K.; Munro, W.; Wang, J.

    1993-01-01

    The expected price of SO 2 emission allowances is an important issue in energy and integrated resource planning activities. For example, the expected price of SO 2 allowances in needed in order to evaluate alternative strategies for meeting SO 2 provisions of the Clean Air Act Amendments of 1990. In addition, the expected SO 2 allowance price is important to state public utility regulators who must provide guidance on rate-making issues regarding utility compliance plans which involve allowance trading and direct investment of SO 2 control technologies. Last but not the least, the expected SO 2 allowance price is an important determinant of the future market for natural gas and low sulfur coal. The paper develops estimates of SO 2 allowance prices over time by constructing national supply and demand curves for SO 2 reductions. Both the supply and demand for SO 2 reductions are based on an analysis of the sulfur content of fuels burned in 1990 by utilities throughout the United States; and on assumptions about plant retirements, the rate of new capacity growth, the types of new and replacement plants constructed, the costs of SO 2 reduction measures and legislation by midwest states to maintain the use of high sulfur coal to protect local jobs. The paper shows that SO 2 allowance prices will peak around the year 2000 at about $500 per ton, and will eventually fall to zero by about the year 2020. A sensitivity analysis indicates that the price of SO 2 allowances is relatively insensitive to assumptions regarding the availability of natural gas or energy demand growth. However, SO 2 allowance prices tend to be quite sensitive to assumptions regarding regulations which may force early retirement of existing power plants and possible legislation which may reduce CO 2 emissions

  11. Direct sulfonation of methane to methanesulfonic acid with SO2 using Ca salts as promoters.

    Science.gov (United States)

    Mukhopadhyay, Sudip; Bell, Alexis T

    2003-04-16

    Direct liquid-phase sulfonation of methane to methanesulfonic acid (MSA) with SO2 has been achieved in triflic acid using K2S2O8 as the oxidant and a small amount of a Ca salt as the promoter. The effects of reaction conditions on the conversion of SO2 to MSA were examined. Included were the influence of solvent acidity, reaction duration, reaction temperature, amount of K2S2O8, and composition and amount of promoters.

  12. A Balloon Sounding Technique for Measuring SO2 Plumes

    Science.gov (United States)

    Morris, Gary A.; Komhyr, Walter D.; Hirokawa, Jun; Lefer, Barry; Krotkov, Nicholay; Ngan, Fong

    2010-01-01

    This paper reports on the development of a new technique for inexpensive measurements of SO2 profiles using a modified dual-ozonesonde instrument payload. The presence of SO2 interferes with the standard electrochemical cell (ECC) ozonesonde measurement, resulting in -1 molecule of O3 reported for each molecule of SO2 present (provided [O3] > [SO2]). In laboratory tests, an SO2 filter made with Cr03 placed on the inlet side of the sonde removes nearly 100% of the SO2 present for concentrations up to 60 ppbv and remained effective after exposure to 2.8 X 10(exp 16) molecules of SO2 [equivalent to a column approximately 150 DU (1 DU = 2.69 X 10(exp 20) molecules m(exp -2))]. Flying two ECC instruments on the same payload with one filtered and the other unfiltered yields SO2 profiles, inferred by subtraction. Laboratory tests and field experience suggest an SO2 detection limit of approximately 3 pbb with profiles valid from the surface to the ozonopause [i.e., approximately (8-10 km)]. Two example profiles demonstrate the success of this technique for both volcanic and industrial plumes.

  13. Reaction behavior of SO2 in the sintering process with flue gas recirculation.

    Science.gov (United States)

    Yu, Zhi-Yuan; Fan, Xiao-Hui; Gan, Min; Chen, Xu-Ling; Chen, Qiang; Huang, Yun-Song

    2016-07-01

    The primary goal of this paper is to reveal the reaction behavior of SO2 in the sinter zone, combustion zone, drying-preheating zone, and over-wet zone during flue gas recirculation (FGR) technique. The results showed that SO2 retention in the sinter zone was associated with free-CaO in the form of CaSO3/CaSO4, and the SO2 adsorption reached a maximum under 900ºC. SO2 in the flue gas came almost from the combustion zone. One reaction behavior was the oxidation of sulfur in the sintering mix when the temperature was between 800 and 1000ºC; the other behavior was the decomposition of sulfite/sulfate when the temperature was over 1000ºC. However, the SO2 adsorption in the sintering bed mainly occurred in the drying-preheating zone, adsorbed by CaCO3, Ca(OH)2, and CaO. When the SO2 adsorption reaction in the drying-preheating zone reached equilibrium, the excess SO2 gas continued to migrate to the over-wet zone and was then absorbed by Ca(OH)2 and H2O. The emission rising point of SO2 moved forward in combustion zone, and the concentration of SO2 emissions significantly increased in the case of flue gas recirculation (FGR) technique. Aiming for the reuse of the sensible heat and a reduction in exhaust gas emission, the FGR technique is proposed in the iron ore sintering process. When using the FGR technique, SO2 emission in exhaust gas gets changed. In practice, the application of the FGR technique in a sinter plant should be cooperative with the flue gas desulfurization (FGD) technique. Thus, it is necessary to study the influence of the FGR technique on SO2 emissions because it will directly influence the demand and design of the FGD system.

  14. SO2 measurements at a high altitude site in the central Himalayas: Role of regional transport

    Science.gov (United States)

    Naja, Manish; Mallik, Chinmay; Sarangi, Tapaswini; Sheel, Varun; Lal, Shyam

    2014-12-01

    Continuous measurements of a climatically important acidic gas, SO2, were made over Nainital (29.37°N, 79.45°E; 1958 m amsl), a regionally representative site in the central Himalayas, for the first time during 2009-2011. Unlike many other sites, the SO2 levels over Nainital are higher during pre-monsoon (345 pptv) compared to winter (71 pptv). High values during pre-monsoon are attributed to the transport of air masses from regions viz. Indo-Gangetic Plain (IGP), northern India and north-East Pakistan, which are dotted with numerous industries and power plants, where coal burning occurs. Transport from the polluted regions is evinced from good correlations of SO2 with wind speed, NOy and UV aerosol index during these periods. Daytime elevations in SO2 levels, influenced by 'valley winds' and boundary layer evolution, is a persistent feature at Nainital. SO2 levels are very much lower during monsoon compared to pre-monsoon, due to oxidation losses and wet scavenging. Despite this, SO2/NOy slopes are high (>0.4) both during pre-monsoon and monsoon, indicating impacts of point sources. The SO2 levels during winter are lower as the measurement site is cut off from the plains due to boundary layer dynamics. Further, the SO2 levels during winter nights are the lowest (lesser than 50 pptv) and resemble free tropospheric conditions.

  15. Simultaneous removal of SO2 and NOX with ammonia absorbent in a packed column

    International Nuclear Information System (INIS)

    Jia, Yong; Du, Daqian; Zhang, Xinxi; Ding, Xilou; Zhong, Oin

    2013-01-01

    Catalytic oxidation of NO followed by simultaneous removal of SO 2 and NO X with ammonia is a promising method for control of coal-fired flue gas pollutants. We investigated simultaneous absorption of SO 2 and NO X in a packed column with ammonia, and found that SO 2 and NO X could promote absorption with each other in the process of simultaneous removal SO 2 and NO X . The removal efficiency of SO 2 and NO X was, respectively, about 98% and 70.9% at pH 5.5, temperature 323.15 K, SO 2 concentration 1,800x10 −6 , NO X concentration 400x10 −6 and m NO2 /m NO 1 in our experimental system. The experimental results also show that the formation of sulfite oxidized by reacting with dissolved NO 2 and the molar ratio of sulfite to total sulfur is more than 0.8 in the solution. Accordingly, the energy consumption for sulfite oxidation would be greatly reduced in the process of simultaneous desulfurization and denitrification with ammonia

  16. Observations of volcanic SO2 from MLS on Aura

    Directory of Open Access Journals (Sweden)

    H. C. Pumphrey

    2015-01-01

    Full Text Available Sulfur dioxide (SO2 is an important atmospheric constituent, particularly in the aftermath of volcanic eruptions. These events can inject large amounts of SO2 into the lower stratosphere, where it is oxidised to form sulfate aerosols; these in turn have a significant effect on the climate. The MLS instrument on the Aura satellite has observed the SO2 mixing ratio in the upper troposphere and lower stratosphere from August 2004 to the present, during which time a number of volcanic eruptions have significantly affected those regions of the atmosphere. We describe the MLS SO2 data and how various volcanic events appear in the data. As the MLS SO2 data are currently not validated we take some initial steps towards their validation. First we establish the level of internal consistency between the three spectral regions in which MLS is sensitive to SO2. We compare SO2 column values calculated from MLS data to total column values reported by the OMI instrument. The agreement is good (within about 1 DU in cases where the SO2 is clearly at altitudes above 147 hPa.

  17. Molecular Dynamics Investigation of Efficient SO2 Absorption by ...

    Indian Academy of Sciences (India)

    ANIRBAN MONDAL

    Ionic liquids are appropriate candidates for the absorption of acid gases such as SO2. Six anion- functionalized ionic liquids with ... Sulfur dioxide (SO2), a significant air pollutant, is mainly emitted from combustion of fossil-fuel and ...... anism of CO2 absorption in phosphonium amino acid ionic liquid RSC Adv. 6 55438. 63.

  18. The US SO2 Auction: Analysis and Generalization

    DEFF Research Database (Denmark)

    Svendsen, Gert Tinggaard; Christensen, J.L.

    1999-01-01

    An annual discriminative and revenue-neutral auction is linked to the new Acid Rain Program which allows electric utilities all over the US to trade SO2 emission permits. This innovative SO2 auction distributes 2% of the permits in circulation and takes place at the Chicago Board of Trade. Early...

  19. On the absolute calibration of SO2 cameras

    Science.gov (United States)

    Lübcke, Peter; Bobrowski, Nicole; Illing, Sebastian; Kern, Christoph; Alvarez Nieves, Jose Manuel; Vogel, Leif; Zielcke, Johannes; Delgados Granados, Hugo; Platt, Ulrich

    2013-01-01

    Sulphur dioxide emission rate measurements are an important tool for volcanic monitoring and eruption risk assessment. The SO2 camera technique remotely measures volcanic emissions by analysing the ultraviolet absorption of SO2 in a narrow spectral window between 300 and 320 nm using solar radiation scattered in the atmosphere. The SO2 absorption is selectively detected by mounting band-pass interference filters in front of a two-dimensional, UV-sensitive CCD detector. One important step for correct SO2 emission rate measurements that can be compared with other measurement techniques is a correct calibration. This requires conversion from the measured optical density to the desired SO2 column density (CD). The conversion factor is most commonly determined by inserting quartz cells (cuvettes) with known amounts of SO2 into the light path. Another calibration method uses an additional narrow field-of-view Differential Optical Absorption Spectroscopy system (NFOVDOAS), which measures the column density simultaneously in a small area of the camera’s field-of-view. This procedure combines the very good spatial and temporal resolution of the SO2 camera technique with the more accurate column densities obtainable from DOAS measurements.

  20. Surface Hydrophobicity Causes SO2 Tolerance in Lichens

    Science.gov (United States)

    Hauck, Markus; Jürgens, Sascha-René; Brinkmann, Martin; Herminghaus, Stephan

    2008-01-01

    Background and Aims The superhydrophobicity of the thallus surface in one of the most SO2-tolerant lichen species, Lecanora conizaeoides, suggests that surface hydrophobicity could be a general feature of lichen symbioses controlling their tolerance to SO2. The study described here tests this hypothesis. Methods Water droplets of the size of a raindrop were placed on the surface of air-dry thalli in 50 lichen species of known SO2 tolerance and contact angles were measured to quantify hydrophobicity. Key Results The wettability of lichen thalli ranges from strongly hydrophobic to strongly hydrophilic. SO2 tolerance of the studied lichen species increased with increasing hydrophobicity of the thallus surface. Extraction of extracellular lichen secondary metabolites with acetone reduced, but did not abolish the hydrophobicity of lichen thalli. Conclusions Surface hydrophobicity is the main factor controlling SO2 tolerance in lichens. It presumably originally evolved as an adaptation to wet habitats preventing the depression of net photosynthesis due to supersaturation of the thallus with water. Hydrophilicity of lichen thalli is an adaptation to dry or humid, but not directly rain-exposed habitats. The crucial role of surface hydrophobicity in SO2 also explains why many markedly SO2-tolerant species are additionally tolerant to other (chemically unrelated) toxic substances including heavy metals. PMID:18077467

  1. Regional differences in Chinese SO2 emission control efficiency and policy implications

    Science.gov (United States)

    Zhang, Q. Q.; Wang, Y.; Ma, Q.; Yao, Y.; Xie, Y.; He, K.

    2015-06-01

    SO2 emission control has been one of the most important air pollution policies in China since 2000. In this study, we assess regional differences in SO2 emission control efficiencies in China through the modeling analysis of four scenarios of SO2 emissions, all of which aim to reduce the national total SO2 emissions by 8% or 2.3 Tg below the 2010 emissions level, the target set by the current twelfth Five-Year Plan (FYP; 2011-2015), but differ in spatial implementation. The GEOS-Chem chemical transport model is used to evaluate the efficiency of each scenario on the basis of four impact metrics: surface SO2 and sulfate concentrations, population-weighted sulfate concentration (PWC), and sulfur export flux from China to the western Pacific. The efficiency of SO2 control (β) is defined as the relative change of each impact metric to a 1% reduction in SO2 emissions from the 2010 baseline. The S1 scenario, which adopts a spatially uniform reduction in SO2 emissions in China, gives a β of 0.99, 0.71, 0.83, and 0.67 for SO2 and sulfate concentrations, PWC, and export flux, respectively. By comparison, the S2 scenario, which implements all the SO2 emissions reduction over North China (NC), is found most effective in reducing national mean surface SO2 and sulfate concentrations and sulfur export fluxes, with β being 1.0, 0.76, and 0.95 respectively. The S3 scenario of implementing all the SO2 emission reduction over South China (SC) has the highest β in reducing PWC (β = 0.98) because SC has the highest correlation between population density and sulfate concentration. Reducing SO2 emissions over Southwest China (SWC) is found to be least efficient on the national scale, albeit with large benefits within the region. The difference in β by scenario is attributable to the regional difference in SO2 oxidation pathways and the source-receptor relationship. Among the three regions examined here, NC shows the largest proportion of sulfate formation through gas

  2. Modeling atmospheric mineral aerosol chemistry to predict heterogeneous photooxidation of SO2

    Science.gov (United States)

    Yu, Zechen; Jang, Myoseon; Park, Jiyeon

    2017-08-01

    The photocatalytic ability of airborne mineral dust particles is known to heterogeneously promote SO2 oxidation, but prediction of this phenomenon is not fully taken into account by current models. In this study, the Atmospheric Mineral Aerosol Reaction (AMAR) model was developed to capture the influence of air-suspended mineral dust particles on sulfate formation in various environments. In the model, SO2 oxidation proceeds in three phases including the gas phase, the inorganic-salted aqueous phase (non-dust phase), and the dust phase. Dust chemistry is described as the absorption-desorption kinetics of SO2 and NOx (partitioning between the gas phase and the multilayer coated dust). The reaction of absorbed SO2 on dust particles occurs via two major paths: autoxidation of SO2 in open air and photocatalytic mechanisms under UV light. The kinetic mechanism of autoxidation was first leveraged using controlled indoor chamber data in the presence of Arizona Test Dust (ATD) particles without UV light, and then extended to photochemistry. With UV light, SO2 photooxidation was promoted by surface oxidants (OH radicals) that are generated via the photocatalysis of semiconducting metal oxides (electron-hole theory) of ATD particles. This photocatalytic rate constant was derived from the integration of the combinational product of the dust absorbance spectrum and wave-dependent actinic flux for the full range of wavelengths of the light source. The predicted concentrations of sulfate and nitrate using the AMAR model agreed well with outdoor chamber data that were produced under natural sunlight. For seven consecutive hours of photooxidation of SO2 in an outdoor chamber, dust chemistry at the low NOx level was attributed to 55 % of total sulfate (56 ppb SO2, 290 µg m-3 ATD, and NOx less than 5 ppb). At high NOx ( > 50 ppb of NOx with low hydrocarbons), sulfate formation was also greatly promoted by dust chemistry, but it was suppressed by the competition between NO2 and SO2

  3. Modeling atmospheric mineral aerosol chemistry to predict heterogeneous photooxidation of SO2

    Directory of Open Access Journals (Sweden)

    Z. Yu

    2017-08-01

    Full Text Available The photocatalytic ability of airborne mineral dust particles is known to heterogeneously promote SO2 oxidation, but prediction of this phenomenon is not fully taken into account by current models. In this study, the Atmospheric Mineral Aerosol Reaction (AMAR model was developed to capture the influence of air-suspended mineral dust particles on sulfate formation in various environments. In the model, SO2 oxidation proceeds in three phases including the gas phase, the inorganic-salted aqueous phase (non-dust phase, and the dust phase. Dust chemistry is described as the absorption–desorption kinetics of SO2 and NOx (partitioning between the gas phase and the multilayer coated dust. The reaction of absorbed SO2 on dust particles occurs via two major paths: autoxidation of SO2 in open air and photocatalytic mechanisms under UV light. The kinetic mechanism of autoxidation was first leveraged using controlled indoor chamber data in the presence of Arizona Test Dust (ATD particles without UV light, and then extended to photochemistry. With UV light, SO2 photooxidation was promoted by surface oxidants (OH radicals that are generated via the photocatalysis of semiconducting metal oxides (electron–hole theory of ATD particles. This photocatalytic rate constant was derived from the integration of the combinational product of the dust absorbance spectrum and wave-dependent actinic flux for the full range of wavelengths of the light source. The predicted concentrations of sulfate and nitrate using the AMAR model agreed well with outdoor chamber data that were produced under natural sunlight. For seven consecutive hours of photooxidation of SO2 in an outdoor chamber, dust chemistry at the low NOx level was attributed to 55 % of total sulfate (56 ppb SO2, 290 µg m−3 ATD, and NOx less than 5 ppb. At high NOx ( >  50 ppb of NOx with low hydrocarbons, sulfate formation was also greatly promoted by dust chemistry, but it was suppressed by

  4. Formation of secondary aerosols from gasoline vehicle exhaust when mixing with SO2

    Directory of Open Access Journals (Sweden)

    T. Liu

    2016-01-01

    Full Text Available Sulfur dioxide (SO2 can enhance the formation of secondary aerosols from biogenic volatile organic compounds (VOCs, but its influence on secondary aerosol formation from anthropogenic VOCs, particularly complex mixtures like vehicle exhaust, remains uncertain. Gasoline vehicle exhaust (GVE and SO2, a typical pollutant from coal burning, are directly co-introduced into a smog chamber, in this study, to investigate the formation of secondary organic aerosols (SOA and sulfate aerosols through photooxidation. New particle formation was enhanced, while substantial sulfate was formed through the oxidation of SO2 in the presence of high concentration of SO2. Homogenous oxidation by OH radicals contributed a negligible fraction to the conversion of SO2 to sulfate, and instead the oxidation by stabilized Criegee intermediates (sCIs, formed from alkenes in the exhaust reacting with ozone, dominated the conversion of SO2. After 5 h of photochemical aging, GVE's SOA production factor revealed an increase by 60–200 % in the presence of high concentration of SO2. The increase could principally be attributed to acid-catalyzed SOA formation as evidenced by the strong positive linear correlation (R2 = 0.97 between the SOA production factor and in situ particle acidity calculated by the AIM-II model. A high-resolution time-of-flight aerosol mass spectrometer (HR-TOF-AMS resolved OA's relatively lower oxygen-to-carbon (O : C (0.44 ± 0.02 and higher hydrogen-to-carbon (H : C (1.40 ± 0.03 molar ratios for the GVE / SO2 mixture, with a significantly lower estimated average carbon oxidation state (OSc of −0.51 ± 0.06 than −0.19 ± 0.08 for GVE alone. The relative higher mass loading of OA in the experiments with SO2 might be a significant explanation for the lower SOA oxidation degree.

  5. Inorganic electrolyte rechargeable Li/SO2 system

    Science.gov (United States)

    Dey, A. N.; Kuo, H. C.; Foster, D.; Schlaikjer, C.; Kallianidis, M.

    An account is given of the chemistry and performance characteristics of prototype inorganic electrolyte Li/SO2-system rechargeable cells. The electrolyte consists of LiAlCl4-6SO2; excellent energy density, rate capability, low temperature performance, storability, and overcharging capability have been obtained, although cell life cycle is thus far limited by the degradation of the microporous polypropylene separator employed. In addition, system safety must be improved to prevent cell thermal runaway upon shorting or external heating.

  6. On the absolute calibration of SO2 cameras

    Directory of Open Access Journals (Sweden)

    P. Lübcke

    2013-03-01

    Full Text Available Sulphur dioxide emission rate measurements are an important tool for volcanic monitoring and eruption risk assessment. The SO2 camera technique remotely measures volcanic emissions by analysing the ultraviolet absorption of SO2 in a narrow spectral window between 300 and 320 nm using solar radiation scattered in the atmosphere. The SO2 absorption is selectively detected by mounting band-pass interference filters in front of a two-dimensional, UV-sensitive CCD detector. One important step for correct SO2 emission rate measurements that can be compared with other measurement techniques is a correct calibration. This requires conversion from the measured optical density to the desired SO2 column density (CD. The conversion factor is most commonly determined by inserting quartz cells (cuvettes with known amounts of SO2 into the light path. Another calibration method uses an additional narrow field-of-view Differential Optical Absorption Spectroscopy system (NFOV-DOAS, which measures the column density simultaneously in a small area of the camera's field-of-view. This procedure combines the very good spatial and temporal resolution of the SO2 camera technique with the more accurate column densities obtainable from DOAS measurements. This work investigates the uncertainty of results gained through the two commonly used, but quite different, calibration methods (DOAS and calibration cells. Measurements with three different instruments, an SO2 camera, a NFOV-DOAS system and an Imaging DOAS (I-DOAS, are presented. We compare the calibration-cell approach with the calibration from the NFOV-DOAS system. The respective results are compared with measurements from an I-DOAS to verify the calibration curve over the spatial extent of the image. The results show that calibration cells, while working fine in some cases, can lead to an overestimation of the SO2 CD by up to 60% compared with CDs from the DOAS measurements. Besides these errors of calibration

  7. Modelling the spatial distribution of SO2 and NO(x) emissions in Ireland

    NARCIS (Netherlands)

    Kluizenaar, Y.de; Aherne, J.; Farrell, E.P.

    2001-01-01

    The spatial distributions of sulphur dioxide (SO2) and nitrogen oxides (NO(x)) emissions are essential inputs to models of atmospheric transport and deposition. Information of this type is required for international negotiations on emission reduction through the critical load approach.

  8. Contribution of SO2 to antioxidant potential of white wine.

    Science.gov (United States)

    Abramovič, Helena; Košmerl, Tatjana; Poklar Ulrih, Nataša; Cigić, Blaž

    2015-05-01

    The reactivity of SO2 with the 2,2-diphenyl-1-picrylhydrazyl radical (DPPH) and in Folin Ciocalteu (FC) assays was analysed under different experimental conditions. There was significantly higher reactivity between SO2 and DPPH in buffered methanol than in methanol alone. When DPPH and FC assays were performed in a mixture of caftaric acid and SO2, there were synergistic effects that were more pronounced with the FC assay. Phenolics are an important parameter of wine quality, and their accurate characterisation in wine is essential. Analysis of white wines with DPPH and FC assays overestimates the contribution of phenolics to the antioxidant potential (AOP). SO2 contributes (from 20% to 45%) to the AOP of the white wines analysed. As SO2 reactivity depends highly on buffer composition, pH, time of incubation and other compounds, e.g. phenolics and aldehydes, different experimental protocols can produce large variations in AOPs, and therefore control of experimental conditions is extremely important. Copyright © 2014. Published by Elsevier Ltd.

  9. Experimental studies on the simultaneous reduction of NO and SO2 emissions by re burning

    International Nuclear Information System (INIS)

    Sun, Rui; Yu, Leibo; Fei, Jun; Mu, Yangyang; Zhang, Xin; Sun, Shaozeng; Wu, Shaohua

    2010-01-01

    The simultaneous reduction of NO and SO 2 by pulverized coal re burning was studied in a drop tube furnace (DTF). A bituminous pulverized coal was chosen as the re burning fuel, and calcium oxide was added as desulfurizer. The influences of stoichiometric ratio (SR), re burning temperature, calcium to sulfur ratio (Ca/ S), and residence time on efficiency of removing NO and SO 2 were studied by DTF hot experiments. The experiment results showed that, at the condition of the re burning temperature 1200 degree Celsius, Ca/ S=1.5, NO reduction efficiency decreased with the increase of re burning fuels stoichiometric ratio, but SO 2 reduction efficiency increased. When the re burning temperature increased from 1000 degree Celsius to 1200 degree Celsius, NO and SO 2 reduction efficiencies initially increased, but then decreased as temperature higher than 1100 degree Celsius. NO reduction efficiency decreased when Ca/ S changed from 1.0 to 2.5, and SO 2 reduction efficiency increased at all times, in spite of the increasing trend became flat when Ca/ S was higher than 2.0. Among all tests, high SO 2 and NO reduction ratios were obtained at SR of 0.8∼0.9 and Ca/ S of 1.5. The mechanisms of desulfurization and denitrification are also discussed and presented to explain the reactions routine in the DTF. (author)

  10. Simultaneous removal of SO2, NO and Hg0 from flue gas by ferrate (VI) solution

    International Nuclear Information System (INIS)

    Zhao, Yi; Han, Yinghui; Guo, Tianxiang; Ma, Tianzhong

    2014-01-01

    Simultaneously removing SO 2 , NO and Hg 0 from flue gas was examined by ferrate (VI) solution at a bubbling reactor. The removal efficiencies of 100% for SO 2 , 64.8% for NO and 81.4% for Hg 0 were achieved respectively, under the optimum experimental conditions, in which concentration of ferrate (VI) solution was 0.25 mmol/L, solution pH was 8.0, flue gas flow rate was 1 L/min and reaction temperature was 320 K. Based on the discussions of the ferrate (VI) solution characteristics, the comparisons of the standard electrode potential (E 0 ) of ferrate (VI) solution with E 0 values of reactant, and the analysis of the reaction products, a mechanism of simultaneous removal was proposed. In the process of simultaneous removal, FeO 4 2− and HFeO 4 − as the dominant species of ferrate (VI), could rapidly oxidize SO 2 , NO, and Hg 0 into SO 4 2− , NO 3 − and Hg 2+ . - Highlights: • Prepared ferrate (VI) absorbent has excellent property of removing SO 2 , NO and Hg 0 . • 100% of SO 2 , 63.8% of NO and 83.6% of Hg 0 were simultaneously removed. • The simultaneous removal mechanism of SO 2 , NO and Hg 0 was proposed

  11. Energy consumption of SO2 removal from humid air under electron beam and electric field influence

    International Nuclear Information System (INIS)

    Nichipor, H.; Radjuk, E.; Chmielewski, A.G.; Zimek, Z.

    1998-01-01

    The kinetic of SO 2 oxidation in humid air under influence of electron beam and electrical field was investigated by computer simulation method in steady state and pulse mode. SO 2 oxidation process was stimulated by radical and ion reactions. The calculation model has included 46 different particles and 160 chemical reactions. Gas mixture containing 1000 ppm of SO 2 concentration was investigated at temperature T=67 deg. C and pressure p=1 at. Water content was within the range 2-12%. Electron beam parameters were as follows: average beam current density 0.0032-3,2 mA/cm 2 , pulse duration 400 μs, repetition rate 50 Hz. Electrical field density was E/n =10 -15 Vcm 2 . Electrical pulse duration was changed within the range 5 x10 -7 -10 -5 s. The influence of the parameters of synchronized electron beam and electrical field pulses on energy deposition was under consideration. Energy cost of SO 2 removal on 90% level was estimated in steady state and pulse modes. It was found that total electron beam and electrical field energy losses in pulse mode are 6 times lower to compare with steady state conditions. The optimum of electrical field pulse duration from point of view minimum energy cost of SO 2 removal was found for different electron beam pulse current levels

  12. Continuous SO2 flux measurements for Vulcano Island, Italy

    Directory of Open Access Journals (Sweden)

    Fabio Vita

    2012-06-01

    Full Text Available The La Fossa cone of Vulcano Island (Aeolian Archipelago, Italy is a closed conduit volcano. Today, Vulcano Island is characterized by sulfataric activity, with a large fumarolic field that is mainly located in the summit area. A scanning differential optical absorption spectroscopy instrument designed by the Optical Sensing Group of Chalmers University of Technology in Göteborg, Sweden, was installed in the framework of the European project "Network for Observation of Volcanic and Atmospheric Change", in March 2008. This study presents the first dataset of SO2 plume fluxes recorded for a closed volcanic system. Between 2008 and 2010, the SO2 fluxes recorded showed average values of 12 t.d–1 during the normal sulfataric activity of Vulcano Island, with one exceptional event of strong degassing that occurred between September and December, 2009, when the SO2 emissions reached up to 100 t.d–1.

  13. Atmospheric Level of SO2 in Sokoto Metropolis, Nigeria * AITsafe ...

    African Journals Online (AJOL)

    acer

    J.T. Ayodele. *Department of Pure and Applied Chemistry, Usmanu Danfodiyo University, Sokoto. **Department of Chemistry, Bayero University, Kano. .... (at 1 atm. and 25 C). RESULTS AND DISCUSSION. The level of SO2 in the atmosphere of Sokoto is mostly as a result of fossil fuel combustion. That is why low levels ...

  14. Evaluation of SO2 compliance strategies at Virginia Power

    International Nuclear Information System (INIS)

    Presley, J.V.; Tomlinson, M.; Ulmer, R.H.

    1992-01-01

    This paper will address the process undertaken by Virginia Power to assess SO 2 control strategies available for complying with the Revised Clean Air Act. In April 1990, in anticipation of the passage of an amended Clean Air Act, Virginia Power assembled a task force of personnel from a wide cross section of the company. This task force was given the responsibility of providing an assessment of the requirements of the new legislation, evaluating compliance alternatives and providing recommendations for implementation of the least cost alternative. Twenty-four potential SO 2 compliance options were identified for evaluation for Phase I. These options included various levels of coal switching, gas co-firing and scrubbing. Each option was evaluated and compared to a base case which assumed no SO 2 control. As a result of our evaluations, the lowest cost and least risk approach to Phase I SO 2 compliance for Virginia Power appears to be to construct a scrubber for one unit (550 MW g ) at our Mt. Storm Power Station

  15. Spatially resolved SO2 flux emissions from Mt Etna

    Science.gov (United States)

    Bitetto, M.; Delle Donne, D.; Tamburello, G.; Battaglia, A.; Coltelli, M.; Patanè, D.; Prestifilippo, M.; Sciotto, M.; Aiuppa, A.

    2016-01-01

    Abstract We report on a systematic record of SO2 flux emissions from individual vents of Etna volcano (Sicily), which we obtained using a permanent UV camera network. Observations were carried out in summer 2014, a period encompassing two eruptive episodes of the New South East Crater (NSEC) and a fissure‐fed eruption in the upper Valle del Bove. We demonstrate that our vent‐resolved SO2 flux time series allow capturing shifts in activity from one vent to another and contribute to our understanding of Etna's shallow plumbing system structure. We find that the fissure eruption contributed ~50,000 t of SO2 or ~30% of the SO2 emitted by the volcano during the 5 July to 10 August eruptive interval. Activity from this eruptive vent gradually vanished on 10 August, marking a switch of degassing toward the NSEC. Onset of degassing at the NSEC was a precursory to explosive paroxysmal activity on 11–15 August. PMID:27773952

  16. The US SO2 Auction and Environmental Regulation

    DEFF Research Database (Denmark)

    Svendsen, Gert Tinggaard; Christensen, J.L.

    1999-01-01

    The US Acid Rain Program (ARP) is now well-established. The ARP relies on tradable permits and includes an annual revenue-neutral SO2 auction. Has this auction been an important factor in establishing low transaction costs and a successful market? In answering this question, we first compare...

  17. Cost-effective control of SO2 emissions in Asia

    NARCIS (Netherlands)

    Cofala, J.; Amann, M.; Gyarfas, F.; Schoepp, F.; Boudri, J.C.; Hordijk, L.; Kroeze, C.; Li Junfeng,; Dai Lin, D.; Panwar, T.S.; Gupta, S.

    2004-01-01

    Despite recent efforts to limit the growth of SO2 emissions in Asia, the negative environmental effects of sulphur emissions are likely to further increase in the future. This paper presents an extension of the RAINS-Asia integrated assessment model for acidification in Asia with an optimisation

  18. Molecular Dynamics Investigation of Efficient SO2 Absorption by ...

    Indian Academy of Sciences (India)

    ANIRBAN MONDAL

    TMG][L]) that absorbs an equimolar amount of SO2 through chemisorption.12 Subsequently, a sig- ...... Visual molecular dynamics J. Mol. Graphics 14 33. 83. Fiorin G, Klein M L and Hénin J 2013 Using collective variables to drive molecular ...

  19. The role of SO2 in volcanism on Io

    Science.gov (United States)

    Smith, B.A.; Shoemaker, E.M.; Kieffer, S.W.; Cook, A.F.

    1979-01-01

    Io and Earth are the only planetary bodies known to be volcanically active; the energetics of the eruptive plumes on Io have important structural implications and are closely linked with the presence of sulphur and SO 2. ?? 1979 Nature Publishing Group.

  20. TiO2 Nanotube Array Sensor for Detecting the SF6 Decomposition Product SO2

    Directory of Open Access Journals (Sweden)

    Ju Tang

    2012-03-01

    Full Text Available The detection of partial discharge through analysis of SF6 gas components in gas-insulated switchgear, is significant for the diagnosis and assessment of the operating state of power equipment. The present study proposes the use of a TiO2 nanotube array sensor for detecting the SF6 decomposition product SO2, and the application of the anodic oxidation method for the directional growth of highly ordered TiO2 nanotube arrays. The sensor response of 10–50 ppm SO2 gas is tested, and the sensitive response mechanism is discussed. The test results show that the TiO2 nanotube sensor array has good response to SO2 gas, and by ultraviolet radiation, the sensor can remove attached components very efficiently, shorten recovery time, reduce chemical poisoning, and prolong the life of the components.

  1. Validation of the SO2 camera for high temporal and spatial resolution monitoring of SO2 emissions

    Science.gov (United States)

    Smekens, Jean-François; Burton, Michael R.; Clarke, Amanda B.

    2015-07-01

    Ground-based measurements of sulfur dioxide (SO2) are a key part of monitoring networks at many volcanic centers. SO2 camera systems represent an attractive addition to conventional spectroscopic methods such as COSPEC or DOAS, because they offer higher sampling rates (up to 1 Hz) and two-dimensional concentration mapping which provides additional contextual information for emission rate calculation and interpretation. Here we present the results of an SO2 camera development project and corresponding validation experiment conducted at a coal-burning power plant in Arizona (USA), where the emissions are independently measured. Emissions of SO2 and other acid gases are regulated in the United States, and hourly data are publicly reported by the US Environmental Protection Agency (EPA). We measured the emissions from two exhaust stacks that had an average combined rate of 8.2 ± 2.1 × 10- 2 kg s- 1 (7 ± 1.8 t d- 1) over a period of 3 h. Masses integrated from our dataset are within 10-20% of the emissions reported by the EPA. The contextual information contained in the images allowed the identification and measurement of the individual plumes from each stack. Measured emission rates decrease with increasing distance from the source, pointing to an apparent loss of SO2 primarily by gas dilution processes, with SO2 concentrations dropping below the detection limit at the edge of the plume at distances > 200 m from the source. Cross-sections very close to the vent (within 50 m; 2 vent diameters), through the optically thick condensing part of the plume, yielded emission rates lower than those reported to the EPA. This near-vent discrepancy is interpreted to be the result of light dilution effects due to attenuation and reflections off the surface of the condensing plume. This work is the first reported validation of emission rate measurements produced by an SO2 camera in a volcano-like geometry, and demonstrates that reliable emission rates can be measured, but also

  2. Radiation processes for the control of NOx/SO2 emissions

    International Nuclear Information System (INIS)

    Dickson, L.W.; Singh, A.

    1988-01-01

    This report provides a brief review of the use of radiation for the treatment of flue gases and identifies areas for additional research. Two different radiation-based processes have been developed for the removal of nitrogen oxides and sulphur dioxide from the flue gases of coal-fired boilers. In the technique developed by the Ebara Corporation and Japan Atomic Energy Research Institute, ammonia is injected prior to the irradiation step to enhance the process efficiency and to yield a solid ammonium sulphate - ammonium nitrate product that may be used as a fertilizer. The process developed by the Research-Cottrell Corporation uses electron-beam irradiation downstream of a lime spray dryer to remove nitrogen oxides and to enhance the sulphur dioxide removal efficiency. Both of these processes require large quantities of electron-beam power and are currently expected to be more expensive than other available sulphur dioxide emission control technologies. Present emission control regulations in North America do not require the high degree of nitrogen oxide removal provided by the radiation-based processes. Research into the radiolytic oxidation of nitrogen oxides and sulphur dioxide, the radiolytic oxidation of NO x /SO 2 on solid sorbents, and the radiolytic oxidation of NO x /SO 2 in electric fields may lead to the development of more economical radiation treatment processes for flue gases. 44 refs

  3. SO2 Spectroscopy with A Tunable UV Laser

    Science.gov (United States)

    Morey, W. W.; Penney, C. M.; Lapp, M.

    1973-01-01

    A portion of the fluorescence spectrum of SO2 has been studied using a narrow wavelength doubled dye laser as the exciting source. One purpose of this study is to evaluate the use of SO2 resonance re-emission as a probe of SO2 in the atmosphere. When the SO2 is excited by light at 300.2 nm, for example, a strong reemission peak is observed which is Stokes-shifted from the incident light wavelength by the usual Raman shift (the VI symmetric vibration frequency 1150.5/cm ). The intensity of this peak is sensitive to small changes (.01 nm) in the incident wavelength. Measurements of the N2 quenching and self quenching of this re-emission have been obtained. Preliminary analysis of this data indicates that the quenching is weak but not negligible. The dye laser in our system is pumped by a pulsed N2 laser. Tuning 'and spectral narrowing are accomplished using a telescope-echelle grating combination. In a high power configuration the resulting pulses have a spectral width of about 5 x 10(exp -3) nm and a time duration of about 6 nsec. The echelle grating is rotated by a digital stepping motor, such that each step shifts the wavelength by 6 x 10(exp -4) nm. In addition to the tunable, narrow wavelength uv source and spectral analysis of the consequent re-emission, the system also provides time resolution of the re-emitted light to 6 nsec resolution. This capability is being used to study the lifetime of low pressure S02 fluorescence at different wavelengths and pressures.

  4. Effect of SO2 Dry Deposition on Porous Dolomitic Limestones

    OpenAIRE

    Olaru, Mihaela; Aflori, Magdalena; Simionescu, Bogdana; Doroftei, Florica; Stratulat, Lacramioara

    2010-01-01

    The present study is concerned with the assessment of the relative resistance of a monumental dolomitic limestone (Laspra – Spain) used as building material in stone monuments and submitted to artificial ageing by SO2 dry deposition in the presence of humidity. To investigate the protection efficiency of different polymeric coatings, three commercially available siloxane-based oligomers (Lotexan-N, Silres BS 290 and Tegosivin HL 100) and a newly synthesized hybrid nanocomposite with silsesqui...

  5. Ab initio calculations of the ionization spectrum of SO2

    International Nuclear Information System (INIS)

    Zhang Yongfeng; Wang Meishan; Yang Chuanlu; Ma Meizhong; Pang Weixiu; Ma Rongcai

    2008-01-01

    The ionization spectrum of sulfur dioxide has been successfully studied by using the symmetry-adapted-cluster configuration-interaction (SAC-CI) general-R and SD-R methods and the basis set correlation-consistent polarized valence triple-zeta (cc-pVTZ). The SAC-CI general-R method reproduces the experimental spectrum well for both the main peaks and the satellite peaks of ionization spectrum of SO 2 . The sequence of ionic states corresponding to main peaks of SO 2 has been re-determined according to the SAC-CI conclusions and it is reordered as X-bar 2 A 1 , Ã 2 B 2 , B-bar 2 A 2 , C-bar 2 B 1 , D-bar 2 A 1 , Ē 2 B 2 and F-bar 2 A 1 . Besides, the equilibrium structures and adiabatic ionization potentials (AIPs) of ionic states of main peaks of SO 2 are calculated by using the SAC-CI SD-R method. (atomic and molecular physics)

  6. CO2-SO2 clathrate hydrate formation on early Mars

    Directory of Open Access Journals (Sweden)

    Chassefière E.

    2014-02-01

    Full Text Available Most sulfate minerals discovered on Mars are dated no earlier than the Hesperian. We showed, using a 1-D radiative-convective-photochemical model, that clathrate formation during the Noachian would have buffered the atmospheric CO2 pressure of early Mars at ~2 bar and maintained a global average surface temperature ~230 K. Because clathrates trap SO2 more favorably than CO2, all volcanically outgassed sulfur would have been trapped in Noachian Mars cryosphere, preventing a significant formation of sulfate minerals during the Noachian and inhibiting carbonates from forming at the surface in acidic water resulting from the local melting of the SO2- rich cryosphere. The massive formation of sulfate minerals at the surface of Mars during the Hesperian could be the consequence of a drop of the CO2 pressure below a 2-bar threshold value at the late Noachian-Hesperian transition, which would have released sulfur gases into the atmosphere from both the Noachian sulfur-rich cryosphere and still active Tharsis volcanism. Our hypothesis could allow to explain the formation of chaotic terrains and outflow channels, and the occurrence of episodic warm episodes facilitated by the release of SO2 to the atmosphere. These episodes could explain the formation of valley networks and the degradation of impact craters, but remain to be confirmed by further modeling.

  7. Forecasting the market for SO2 emission allowances under uncertainty

    International Nuclear Information System (INIS)

    Hanson, D.; Molburg, J.; Fisher, R.; Boyd, G.; Pandola, G.; Lurie, G.; Taxon, T.

    1991-01-01

    This paper deals with the effects of uncertainty and risk aversion on market outcomes for SO 2 emission allowance prices and on electric utility compliance choices. The 1990 Clean Air Act Amendments (CAAA), which are briefly reviewed here, provide for about twice as many SO 2 allowances to be issued per year in Phase 1 (1995--1999) than in Phase 2. Considering the scrubber incentives in Phase 1, there is likely to be substantial emission banking for use in Phase 2. Allowance prices are expected to increase over time at a rate less than the return on alternative investments, so utilities which are risk neutral, or potential speculators in the allowance market, are not expected to bank allowances. The allowances will be banked by utilities that are risk averse. The Argonne Utility Simulation Model (ARGUS2) is being revised to incorporate the provisions of the CAAA acid rain title and to simulate SO 2 allowance prices, compliance choices, capacity expansion, system dispatch, fuel use, and emissions using a unit level data base and alternative scenario assumptions. 1 fig

  8. A Method for the Simultaneous Cleansing of H2S and SO2

    Directory of Open Access Journals (Sweden)

    Dzhamal R. Uzun

    2016-01-01

    Full Text Available A method for the simultaneous electrochemical purification of hydrogen sulfide and sulfur dioxide from sea water or industrial wastes is proposed. Fundamentally the method is based on the electrochemical affinity of the pair H2S and SO2. The reactions (oxidation of H2S and reduction of SO2 proceed on а proper catalyst in a flow reactor, without an external power by electrochemical means. The partial curves of oxidation of H2S and reduction of SO2 have been studied electrochemically on different catalysts. Following the additive principle the rate of the process has been found by intersection of the curves. The overall process rate has been studied in a flow type reactor. Similar values of the process rate have been found and these prove the electrochemical mechanism of the reactions. As a result the electrochemical method at adequate conditions is developed. The process is able to completely convert the initial reagents (concentrations CH2S, SO2=0, which is difficult given the chemical kinetics.

  9. Emission of SO2 and NOx from power plants

    International Nuclear Information System (INIS)

    Boll Illerup, J.; Bruun, H.G.

    2003-01-01

    The European Parliament and the European Council have issued the directive on the limitation of emissions of certain pollutants into the air from large combustion plants (LCP directive, 2001/80/EC of 23 October 2001). The objective of the directive is to control and reduce emissions of SO 2 and NO X , to keep depositions and concentrations below the critical loads and levels. The directive was implemented in Denmark in 2002 and replaces Statutory Order no. 689 of 15 October 1990 about reduction of SO 2 , NO X and particulate matter from large combustion plants. The purpose of the project is to evaluate whether the emission limit values laid down by the LCP directive will - to the same extent as the Statutory Order from the Danish Energy Agency on emission quota for power plants - ensure the fulfilment of Denmark's obligations in relation to the EU directive on national emission ceilings and the similar obligations in the UNECE Gothenburg Protocol. The emission ceilings for Denmark in 2010 are 55,000 tons SO 2 and 127,000 tons NO X The project includes the power plants regulated by the quota law, which means all plants larger than 25 MWe. The emissions are calculated for three production scenarios: 1) the national supply scenario where the produced electricity equals the electricity used in Denmark, 2) the low price scenario with little export of electricity in the ELSAM area and little import in the Energi E2 area, and 3) the high price scenario with large export of electricity. The emissions are estimated from emission factors based on the LCP directive and emission factors based on a valuation of the actual concentration of SO, and NOX in the flue gas. If the emissions from the power plants just comply with the emission limit values given in the directive the total emissions of both SO 2 and NO X are higher than the quota for all three scenarios. If the emissions are assumed to depend on the actual technological status in 2010 at individual plants, e.g. installed

  10. SO2 photolysis as a source for sulfur mass-independent isotope signatures in stratospehric aerosols

    Directory of Open Access Journals (Sweden)

    A. R. Whitehill

    2015-02-01

    stratospheric sulfate aerosols and provides a minor, but important, oxidation pathway for stratospheric SO2. The production and preservation of S-MIF signals requires a high SO2 column density to allow for optical isotopologue screening effects to occur and to generate a large enough signature that it can be preserved. In addition, the SO2 plume must reach an altitude of around 20 to 25 km, where SO2 photolysis becomes a dominant process. These experiments are the first step towards understanding the origin of the sulfur isotope anomalies in stratospheric sulfate aerosols.

  11. MLS/Aura Near-Real-Time L2 Sulfur Dioxide (SO2) Mixing Ratio V003 (ML2SO2_NRT) at GES DISC

    Data.gov (United States)

    National Aeronautics and Space Administration — ML2SO2_NRT is the EOS Aura Microwave Limb Sounder (MLS) Near-Real-Time (NRT) product for sulfur dioxide (SO2). This product contains daily SO2 profiles derived from...

  12. Market Opportunities for Austenitic Stainless Steels in SO2 Scrubbers

    Science.gov (United States)

    Michels, Harold T.

    1980-10-01

    Recent U.S. federal legislation has created new opportunities for SO2 scrubbers because all coals, even low-sulfur western coals, will probably require scrubbing to remove SO2 from gaseous combustion products. Scrubbing, the chemical absorption of SO2 by vigorous contact with a slurry—usually lime or limestone—creates an aggressive acid-chloride solution. This presents a promising market for pitting-resistant austenitic stainless steels, but there is active competition from rubber and fiberglass-lined carbon steel. Since the latter are favored on a first-cost basis, stainless steels must be justified on a cost/performance or life-cost basis. Nickel-containing austenitic alloys are favored because of superior field fabricability. Ferritic stainless steels have little utility in this application because of limitations in weldability and resulting poor corrosion resistance. Inco corrosion test spools indicate that molybdenum-containing austenitic alloys are needed. The leanest alloys for this application are 316L and 317L. Low-carbon grades of stainless steel are specified to minimize corrosion in the vicinity of welds. More highly alloyed materials may be required in critical areas. At present, 16,000 MW of scrubber capacity is operational and 17,000 MW is under construction. Another 29,000 MW is planned, bringing the total to 62,000 MW. Some 160,000 MW of scrubber capacity is expected to be placed in service over the next 10 years. This could translate into a total potential market of 80,000 tons of alloy plate for new power industry construction in the next decade. Retrofitting of existing power plants plus scrubbers for other applications such as inert gas generators for oil tankers, smelters, municipal incinerators, coke ovens, the pulp and paper industry, sulfuric acid plants, and fluoride control in phosphoric acid plants will add to this large market.

  13. DSCOVR/EPIC observations of SO2 reveal dynamics of young volcanic eruption clouds

    Science.gov (United States)

    Carn, S. A.; Krotkov, N. A.; Taylor, S.; Fisher, B. L.; Li, C.; Bhartia, P. K.; Prata, F. J.

    2017-12-01

    clouds, such as the relative roles of H2S oxidation and ice scavenging in modifying volcanic SO2 emissions. Detection of these relatively small events also proves EPIC's ability to provide timely detection of volcanic clouds in the upper troposphere and lower stratosphere.

  14. Mass-transport limitation to in-cloud reaction rates: Implications of new accommodation coefficient measurements

    International Nuclear Information System (INIS)

    Schwartz, S.E.

    1988-10-01

    Although it has been recognized for some time that the rate of reactive uptake of gases in cloudwater can depend on the value of the mass-accommodation coefficient (α) describing interfacial mass transport (MT), definitive evaluation of such rates is only now becoming possible with the availability of measurements of α for gases of atmospheric interest at air-water interfaces. Examination of MT limitation to the rate of in-cloud aqueous-phase oxidation of SO 2 by O 3 and H 2 O 2 shows that despite the low value of α/sub O3/ (5 /times/ 10/sup /minus/4/), interfacial MT of this species is not limiting under essentially all conditions of interest; the high values of α for SO 2 (≥ 0.2) and H 2 O 2 (≥ 0.08) indicate no interfacial MT limitation for these species also. Although gas- and aqueous-phase MT can be limiting under certain extremes of conditions, treating the system as under chemical kinetic control is generally an excellent approximation. Interfacial MT limitation also is found not to hinder the rate of H 2 O 2 formation by aqueous-phase disproportionation of HO 2 . Finally, the rapid uptake of N 2 O 5 by cloud droplets implies that the yield of aqueous HNO 3 from in-cloud gas-phase oxidation of NO 2 by O 3 can be substantial even under daytime conditions. This report consists of copies of viewgraphs prepared for this presentation

  15. Anthropogenic SO2/NOx committee--current status

    International Nuclear Information System (INIS)

    Benkovitz, C.M.

    1993-04-01

    Current activities of the Anthropogenic SO 2 /NO x Committee center around the compilation of Version 1 of the GEIA inventories. These inventories will be based on the GEIA-specified 1 degrees by 1 degrees grid (lower left corner at 180 degrees W/90 degrees S, west to east and south to north), reflect 1985 emissions and consist of two data sets: Version 1A inventories with annual emissions at one level and Version 1B inventories with seasonal emissions, two vertical levels (defined at 100 m) and sectoral split information. The basic information used for both versions of the GEIA inventories will be identical; i.e., emissions totals across both inventories will be the same. Work is being carried out in two complementary working groups; Carmen Benkovitz, Brookhaven National Laboratory, Upton, NY, USA heads the work on the annual inventory, Eva Voldner, Atmospheric Environment Services, Canada and Trevor Scholtz, ORTECH International, Canada, head the work on the seasonal inventory

  16. Io's Thermal Regions and Non-SO2 Spectral Features

    Science.gov (United States)

    Smythe, W. D.; Soderblom, L. A.; Lopes, R. M. C.

    2003-01-01

    Several absorptions have been identified in the Galileo NIMS spectra of Io that are not related to SO2. [1,2]. These absorptions have band centers at 2.97, 3.15, 3.85, and 3.91 microns. There are also broad absorptions in the regions 1-1.3 and 3- 3.4 microns. Patterning noise in wavelength registration, arising from the pushbroom imaging and grating motion of the NIMS instrument have previously inhibited reliable mapping of weak absorptions. Recent improvements in techniques to remove the coherent pattern noise from the NIMS dataset have been made by Soderblom. This greatly improves the signal to noise ratio and enables mapping of weak spectral signatures such as the 3.15 micron absorption on Io.

  17. High-Temperature Release of SO2 from Calcined Cement Raw Materials

    DEFF Research Database (Denmark)

    Nielsen, Anders Rooma; Larsen, Morten B.; Glarborg, Peter

    2011-01-01

    During combustion of alternative fuels in the material inlet end of cement rotary kilns, local reducing conditions may occur and cause reductive decomposition of sulfates from calcined cement raw materials. Decomposition of sulfates is problematic because it increases the gas-phase SO2 concentrat......During combustion of alternative fuels in the material inlet end of cement rotary kilns, local reducing conditions may occur and cause reductive decomposition of sulfates from calcined cement raw materials. Decomposition of sulfates is problematic because it increases the gas-phase SO2...... concentration, which may cause deposit formation in the kiln system. In this study, the release of sulfur from calcined cement raw materials under both oxidizing and reducing conditions is investigated. The investigations include thermodynamic equilibrium calculations in the temperature interval of 800–1500 °C...

  18. SO2 policy and input substitution under spatial monopoly

    International Nuclear Information System (INIS)

    Gerking, Shelby; Hamilton, Stephen F.

    2010-01-01

    Following the U.S. Clean Air Act Amendments of 1990, electric utilities dramatically increased their utilization of low-sulfur coal from the Powder River Basin (PRB). Recent studies indicate that railroads hauling PRB coal exercise a substantial degree of market power and that relative price changes in the mining and transportation sectors were contributing factors to the observed pattern of input substitution. This paper asks the related question: To what extent does more stringent SO 2 policy stimulate input substitution from high-sulfur coal to low-sulfur coal when railroads hauling low-sulfur coal exercise spatial monopoly power? The question underpins the effectiveness of incentive-based environmental policies given the essential role of market performance in input, output, and abatement markets in determining the social cost of regulation. Our analysis indicates that environmental regulation leads to negligible input substitution effects when clean and dirty inputs are highly substitutable and the clean input market is mediated by a spatial monopolist. (author)

  19. Making a market for SO2 emissions trading

    International Nuclear Information System (INIS)

    Solomon, B.D.; Rose, K.

    1992-01-01

    Under the innovative, market-based approach to acid rain control included in the Clean Air Act amendments of 1990 (CAAA), sulfur dioxide emission allowances allocated to existing electric utility sources of these emissions can be used by utilities, banked for future use, or sold or traded to other users. Most power plants that burn fossil fuels will need to obtain an adequate supply of allowances from the market of EPA-sponsored auctions to cover their future emissions. This article addresses the respective roles of regulators and the private sector in facilitating a market for SO 2 emission allowances. In previous work, the authors have argued that state public utility commissions should seize the opportunity to encourage utilities to facilitate the allowance market. Yet it is the nature of new markets that many potential participants (including regulators) are risk-averse and wait for others to make the first move. Taken to the extreme, such behavior is a prescription for failure. The authors stated purpose is both to offer a perspective on how to make a market for what was previously considered an externality, as well as to stimulate debate among the various players and elicit better ideas. In fact, much more may be at stake. The success or failure of the emissions trading program could well set a benchmark for future environmental protection efforts in the US and globally

  20. Low SO2 Emission Preheaters for Cement Production

    DEFF Research Database (Denmark)

    Rasmussen, Martin Hagsted

    at low temperatures resulted in the largest surface area, about 140 m2/g CaO. The material produced from all of the methods was a mixture of CaO and CaCO3, meaning that the material was only partly calcined, but with the particle surface area being comprised by CaO. One focus in this thesis...... second, which was possible using an entrained flow reactor. Furthermore, the experimental results were found to be limited by both external and internal diffusion. The reaction product was identified as a mixture of CaSO3 and CaSO4. For temperatures below 600 °C no effect from O2 was observed. At low CO2...... reaction between SO2 and CaO is so fast that the observed rates exclusively are determined by solid state diffusion in the product layer of the non-porous CaO grains. An activation energy of 115 kJ/mole was found to fit all CaO sources very well, even though data fitting by the least sum of squares method...

  1. Debunking the myths: Natural gas and SO2 allowance solutions

    International Nuclear Information System (INIS)

    Roberts, G.D. Jr.

    1993-01-01

    During the decade of the 1990's and beyond, natural gas is expected to be the fuel of choice for a significant portion of new generation capacity. Natural gas already enjoys a greater than 50% market share as a fuel source in the non-regulated cogeneration and Independent Power Producer market. With the new administration in Washington, increased environmental focus will likely increase the attractiveness of natural gas based capacity expansions. While these various issues may appear to contribute to making this decade, the decade for natural gas, there are a number of challenges that must be met if the natural gas and power generation industries are going to satisfy the ever increasing needs of the marketplace. These challenges include: (1) myths of natural gas supply availability, (2) transportation and operational coordination issues, (3) uncertainty of price and reliability, and (4) natural gas for NO x and SO 2 compliance. The author believes that these challenges are actively being met and that there are existing solutions already being offered and incorporated into contracts by natural gas suppliers. The focus of this paper is how electric utilities need to become comfortable with the new natural gas industry and how services can be structured to meet these challenges of serving the electric market requirements

  2. Atmospheric Level of SO2 in Sokoto Metropolis, Nigeria | Tsafe ...

    African Journals Online (AJOL)

    The concentration of atmospheric sulphur (IV) oxide in Sokoto Metropolis was determined by sucking air in hydrogen peroxide solution, followed by the photometric determination of the sulphates ion formed. The overall mean concentration obtained (0.270+-0.051 mg/m3) exceeds the recommended WHO daily guideline ...

  3. Reactions of SO 2 on hydrated cement particle system for atmospheric pollution reduction: A DRIFTS and XANES study

    Energy Technology Data Exchange (ETDEWEB)

    Ramakrishnan, Girish; Wu, Qiyuan; Moon, Juhyuk; Orlov, Alexander

    2017-07-01

    An investigation of the adsorptive property of hydrated cement particle system for sulfur dioxide (SO2) removal was conducted. In situ and ex situ experiments using Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) and X-ray Absorption Near Edge Spectroscopy (XANES) characterization techniques were employed to identify surface species formed during the exposure to SO2. Oxidation of SO2 to sulfate and sulfite species observed during these experiments indicated dominant reaction pathways for SO2 reaction with concrete constituents, such as calcium hydroxide, which were also moderated by adsorption on porous surfaces of crushed aggregates. The impact of variable composition of concrete on its adsorption capacity and reaction mechanisms was also proposed in this work.

  4. An investigation of sulfate production in clouds using a flow-through chemical reactor model approach

    Science.gov (United States)

    Hong, M. S.; Carmichael, G. R.

    1983-01-01

    A flow-through chemical reactor model is developed to describe the mass transfer and chemical processes that atmospheric gases undergo in clouds. The model includes the simultaneous absorption of SO2, NH3, O3, NO(x), HNO3, CO2 and H2O2, the accompanying dissociation and oxidation reactions in cloud water, considers electrical neutrality, and includes qualitative parameterization of cloud microphysics. The model is used to assess the importance of the oxidation reactions H2O2-S(IV), O3-S(IV), and S(IV)-Mn(2+) catalysis, and the effects of cloud parameters such as drop size, rain intensity, liquid water content, and updraft velocity. Both precipitating and nonprecipitating clouds are studied. Model results predict sulfate production rates varying from 3 percent/hr to 230 percent/hr. The actual rate is highly dependent on the chemical composition of the uptake air and the physical conditions of the cloud. Model results also show that both the H2O2 and the O3 oxidation reactions can be significant.

  5. 40 CFR 97.286 - Withdrawal from CAIR SO2 Trading Program.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 20 2010-07-01 2010-07-01 false Withdrawal from CAIR SO2 Trading... PROGRAMS (CONTINUED) FEDERAL NOX BUDGET TRADING PROGRAM AND CAIR NOX AND SO2 TRADING PROGRAMS CAIR SO2 Opt-in Units § 97.286 Withdrawal from CAIR SO2 Trading Program. Except as provided under paragraph (g) of...

  6. 40 CFR 96.286 - Withdrawal from CAIR SO2 Trading Program.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 20 2010-07-01 2010-07-01 false Withdrawal from CAIR SO2 Trading... PROGRAMS (CONTINUED) NOX BUDGET TRADING PROGRAM AND CAIR NOX AND SO2 TRADING PROGRAMS FOR STATE IMPLEMENTATION PLANS CAIR SO2 Opt-in Units § 96.286 Withdrawal from CAIR SO2 Trading Program. Except as provided...

  7. Present status and trends in SO2 and NOx emission control regulations in Europe

    International Nuclear Information System (INIS)

    Ellison, W.

    1987-01-01

    1983 West German legislation (GFAVO) calls for retrofitting by 1988 of FGD facilities of a minimum of 85% sulfur dioxide (SO2) removal efficiency, with stack emission no greater than 400 milligrams (mg) per normal cubic meter (Nm 3 ) of flue gas, for new and existing boilers greater than approximately 110 megawatts i.e. MW(e), size. As of 1986, more than 100 FGD systems with greater than 40,000 MW(e) aggregate capacity have been purchased in West Germany alone. 1983 West German legislation requires by 1993 the retrofit addition of approximately 400 more FGD installations aggregating approximately 25,000 MW(e) of capacity on boilers in the size range 35 to 110 MW(e). Stringent West German SO2 legislation in 1983 was followed in 1984 by enactment of very strict new nitrogen oxides (NOx) limits calling for emissions of no more than 200 mg NOx, measured as nitrogen dioxide, NO2, per Nm 3 , approximately 0.16 lb NO2 per million Btu heat input, for existing and new boilers greater than 110 MW(e), size. As of 1986 approximately 50 high-efficiency commercial systems aggregating more than 10,000 MW(e) capacity, most for retrofit addition, have been purchased in West Germany alone, and approximately 30,000 MW(e) of additional NOx removal capacity will be required to be retrofitted by deadlines during the period 1988 to 1990. For comparative purposes a brief description is given of regulations in North America for control of SO2 and NOx emissions from large coal-fired boilers

  8. Na3.4Zr1.8Mg0.2Si2PO12 filled poly(ethylene oxide)/Na(CF3SO2)2N as flexible composite polymer electrolyte for solid-state sodium batteries

    Science.gov (United States)

    Zhang, Zhizhen; Xu, Kaiqi; Rong, Xiaohui; Hu, Yong-Sheng; Li, Hong; Huang, Xuejie; Chen, Liquan

    2017-12-01

    Solid electrolytes with high ionic conductivity and excellent electrochemical stability are of prime significance to enable the application of solid-state batteries in energy storage and conversion. In this study, solid composite polymer electrolytes (CPEs) based on sodium bis(trifluorosulfonyl) imide (NaTFSI) and poly (ethylene oxide) (PEO) incorporated with active ceramic filler (NASICON) are reported for the first time. With the addition of NASICON fillers, the thermal stability and electrochemical stability of the CPEs are improved. A high conductivity of 2.8 mS/cm (at 80 °C) is readily achieved when the content of the NASICON filler in the composite polymer reaches 50 wt%. Furthermore, Na3V2(PO4)3/CPE/Na solid-state batteries using this composite electrolyte display good rate and excellent cycle performance.

  9. Modelling and experimentation of the SO2 remotion through a plasma out of thermal equilibrium

    International Nuclear Information System (INIS)

    Moreno S, H.; Pacheco P, M.; Pacheco S, J.; Cruz A, A.

    2005-01-01

    In spite of the measures that have taken for the decrease of the emitted pollution by mobile sources ( T oday it doesn't Circulate , implementation of catalysts in those exhaust pipes,...), the pollution in the Valley of Mexico area overcomes the limits fixed by Mexican standards several days each year. It is foreseen that for 2020 those emissions of pollutants will be increase considerably, as example we can mention to the sulfur oxides which will be increase a 48% with regard to 1998. The purpose of this work is of proposing a technique for the degradation of the sulfur dioxide (SO 2 ) that consists in introducing this gas to a plasma out of thermal equilibrium where its were formed key radicals (O, OH) for its degradation. The proposed reactor has the advantage of combining the kindness of the dielectric barrier discharge and of corona discharge, besides working to atmospheric pressure and having small dimensions. The first obtained results of the modelling of the degradation of the SO 2 in plasma as well as those experimentally obtained are presented. (Author)

  10. Top-down NOx and SO2 emissions simultaneously estimated from different OMI retrievals and inversion frameworks

    Science.gov (United States)

    Qu, Z.; Henze, D. K.; Wang, J.; Xu, X.; Wang, Y.

    2017-12-01

    Quantifying emissions trends of nitrogen oxides (NOx) and sulfur dioxide (SO2) is important for improving understanding of air pollution and the effectiveness of emission control strategies. We estimate long-term (2005-2016) global (2° x 2.5° resolution) and regional (North America and East Asia at 0.5° x 0.667° resolution) NOx emissions using a recently developed hybrid (mass-balance / 4D-Var) method with GEOS-Chem. NASA standard product and DOMINO retrievals of NO2 column are both used to constrain emissions; comparison of these results provides insight into regions where trends are most robust with respect to retrieval uncertainties, and highlights regions where seemingly significant trends are retrieval-specific. To incorporate chemical interactions among species, we extend our hybrid method to assimilate NO2 and SO2 observations and optimize NOx and SO2 emissions simultaneously. Due to chemical interactions, inclusion of SO2 observations leads to 30% grid-scale differences in posterior NOx emissions compared to those constrained only by NO2 observations. When assimilating and optimizing both species in pseudo observation tests, the sum of the normalized mean squared error (compared to the true emissions) of NOx and SO2 posterior emissions are 54-63% smaller than when observing/constraining a single species. NOx and SO2 emissions are also correlated through the amount of fuel combustion. To incorporate this correlation into the inversion, we optimize seven sector-specific emission scaling factors, including industry, energy, residential, aviation, transportation, shipping and agriculture. We compare posterior emissions from inversions optimizing only species' emissions, only sector-based emissions, and both species' and sector-based emissions. In situ measurements of NOx and SO2 are applied to evaluate the performance of these inversions. The impacts of the inversion on PM2.5 and O3 concentrations and premature deaths are also evaluated.

  11. piSCOPE - A Python based software package for the analysis of volcanic SO2 emissions using UV SO2 cameras

    Science.gov (United States)

    Gliss, J.; Stebel, K.; Kylling, A.; Skauli, T.; Sudbø, A.

    2016-12-01

    In the past years, the use of UV SO2 cameras rapidly increased in importance for the quantification of volcanic SO2 emissions. UV SO2 cameras measure scattered solar UV radiation in two wavelength windows, typically around 310 nm and 330 nm (strong / negligible SO2 absorption) using dichroic filters. The 330 nm filter is to correct for potential spectral broadband variations, for instance due to aerosols. The plume images in both channels are analysed with respect to the ambient sky intensity. The resulting optical density images are converted into SO2 column density (CD) images either using SO2 gas cells or spectral data (e.g. from a DOAS instrument) for calibration. SO2 emission fluxes are then determined along a plume cross section by integrating the product of SO2-CDs and plume speed. piSCOPE (python image analysis Software for Camera Observation of Plume Emissions) is a Python based open source, cross-platform software library for the analysis of SO2 camera data including a GUI application for interactive analysis. The idea and it's main purpose is to provide a common and fully transparent platform based on current analysis standards to encourage scientific exchange and further method development with regard to the analysis of UV SO2 camera data. piSCOPE provides high level convenience functionality and I/O routines for standard image formats and supplementary data (e.g. import of spectral results, live access to volcano database, access to high resolution topography data) as well as fast routines for SO2 flux retrievals. This includes algorithms for geometrical calculations (e.g. distance to plume / topography on a pixel base), image pre-processing (e.g. dark correction, noise reduction), background image modelling, cell and DOAS calibration, a routine for light dilution correction and pixel based plume speed retrievals (optical flow). All algorithms are either based on latest research findings or were newly developed. Thus, piSCOPE is an important step

  12. 40 CFR Appendix C to Part 72 - Actual 1985 Yearly SO2 Emissions Calculation

    Science.gov (United States)

    2010-07-01

    ... Calculation C Appendix C to Part 72 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Emissions Calculation The equation used to calculate the yearly SO2 emissions (SO2) is as follows: SO2.... fact.) × (yearly fuel burned) For coal, the yearly fuel burned is in tons/yr and the AP-42 factor...

  13. Effect of SO2 concentration on SOA formation in a photorreactor from a mixture of anthropogenic hydrocarbons and HONO

    Science.gov (United States)

    García Vivanco, Marta; Santiago, Manuel; García Diego, Cristina; Borrás, Esther; Ródenas, Milagros; Martínez-Tarifa, Adela

    2010-05-01

    Sulfur dioxide (SO2) is an important urban atmospheric pollutant, mainly produced by the combustion of fossil fuels containing sulfur. In the atmosphere, SO2 can react with OH radicals to form sulfuric acid, which can condense to form acidic aerosol. Sulfuric acid particles act as an acid catalyst for some heterogeneous carbonyl reactions like hydration, polymerization or acetals formation, which may lead to a large increase on SOA mass. In order to evaluate the effect of the SO2 concentration on SOA formation, 3 experiments were performed during the campaign carried out by CIEMAT on the EUPHORE facility (CEAM, Valencia, Spain) during June- July 2008. The objective of the campaign was to evaluate the effect of different experimental conditions on SOA formation from the photooxidation of some anthropogenic and biogenic VOCs using HONO as oxidant. Experiment on 6/17/08 was selected as base case (no SO2 was introduced) and experiments 6/26/08 and 7/1/08 were selected as high SO2 (2600 ug/m3) and low SO2 (60 ug/m3) concentration experiments respectively. In the three experiments a mixture of toluene, 1,3,5-TMB (trimethylbenzene), o-xylene and octane was selected as the parent VOCs. Single and coupled to mass spectroscopy gas cromatography (GC and GC/MS), as well as high performance liquid chromatography (HPLC) and Fourier transform infrared spectroscopy (FTIR) were used to measure the initial VOCs and oxidant concentrations decay and the formation of gas phase oxidation products through the experiments. Aerosol size distribution and concentration were measured with SMPS (scanning mobility particle sizer) and TEOM (tapered element oscillating monitor) respectively. In addition, analysis of the organic and inorganic aerosol content was also performed via filter sampling followed by GC/MS and ionic chromatography (for organic and inrganic content respectively). Comparing the filters collected in the three experiments, clearly the largest mass aerosol formation is observed

  14. Impact of burning oil as auxiliary fuel in kraft recovery furnaces upon SO2 emissions

    International Nuclear Information System (INIS)

    Someshwar, A.V.; Caron, A.L.; Pinkerton, J.E.

    1990-01-01

    The relationship between burning medium sulfur oil as auxiliary fuel in kraft recovery furnaces and SO 2 emissions was examined. Analysis of long-term CEMS SO 2 data from four furnaces shows no increase in SO 2 emissions as a result of oil burning. The results of field tests conducted at four furnaces while co-firing oil with liquor (up to 34% of total heat input) show that (1) average SO 2 emissions during the oil firing period either decreased or remained unchanged; (2) the overall sulfur retention within the furnace remained consistently high (more than 90%) with increasing levels of oil burning; (3) apportioning stack SO 2 emissions between those derived from oil and black liquor was infeasible. The results indicate that the same alkali fume generation processes that lead to the efficient capture of SO 2 resulting from black liquor combustion may be responsible for the capture of SO 2 resulting from sulfur-containing oil combustion

  15. SO2 columns over China: Temporal and spatial variations using OMI and GOME-2 observations

    Science.gov (United States)

    Huanhuan, Yan; Liangfu, Chen; Lin, Su; Jinhua, Tao; Chao, Yu

    2014-03-01

    Enhancements of SO2 column amounts due to anthropogenic emission sources over China were shown in this paper by using OMI and GOME-2 observations. The temporal and spatial variations of SO2 columns over China were analyzed for the time period 2005-2010. Beijing and Chongqing showed a high concentration in the SO2 columns, attributable to the use of coal for power generation in China and the characteristic of terrain and meteorology. The reduction of SO2 columns over Beijing and surrounding provinces in 2008 was observed by OMI, which confirms the effectiveness of strict controls on pollutant emissions and motor vehicle traffic before and during 2008 Olympic and Paralympic Games. The SO2 columns over China from GOME-2 (0.2-0.5 DU) were lower than those from OMI (0.6-1 DU), but both showed a decrease in SO2 columns over northern China since 2008 (except an increase in OMI SO2 in 2010).

  16. Interaction of SO2 with the Surface of a Water Nanodroplet.

    Science.gov (United States)

    Zhong, Jie; Zhu, Chongqin; Li, Lei; Richmond, Geraldine L; Francisco, Joseph S; Zeng, Xiao Cheng

    2017-11-29

    We present a comprehensive computational study of interaction of a SO 2 with water molecules in the gas phase and with the surface of various sized water nanodroplets to investigate the solvation behavior of SO 2 in different atmospheric environments. Born-Oppenheimer molecular dynamics (BOMD) simulation shows that, in the gas phase and at a temperature of 300 K, the dominant interaction between SO 2 and H 2 O is (SO 2 ) S···O (H 2 O) , consistent with previous density-functional theory (DFT) computation at 0 K. However, at the surface of a water nanodroplet, BOMD simulation shows that the hydrogen-bonding interaction of (SO 2 ) O···H (H 2 O) becomes increasingly important with the increase of droplet size, reflecting a marked effect of the water surface on the SO 2 solvation. This conclusion is in good accordance with spectroscopy evidence obtained previously (J. Am. Chem. Soc. 2005, 127, 16806; J. Am. Chem. Soc. 2006, 128, 3256). The prevailing interaction (SO 2 ) O···H (H 2 O) on a large droplet is mainly due to favorable exposure of H atoms of H 2 O at the air-water interface. Indeed, the conversion of the dominant interaction in the gas phase (SO 2 ) S···O (H 2 O) to the dominant interaction on the water nanodroplet (SO 2 ) O···H (H 2 O) may incur effects on the SO 2 chemistry in atmospheric aerosols because the solvation of SO 2 at the water surface can affect the reactive sites and electrophilicity of SO 2 . Hence, the solvation of SO 2 on the aerosol surface may have new implications when studying SO 2 chemistry in the aerosol-containing troposphere.

  17. SO2 flux monitoring at Stromboli with the new permanent INGV SO2 camera system: A comparison with the FLAME network and seismological data

    Science.gov (United States)

    Burton, M. R.; Salerno, G. G.; D'Auria, L.; Caltabiano, T.; Murè, F.; Maugeri, R.

    2015-07-01

    We installed a permanent SO2 camera system on Stromboli, Italy, in May 2013, in order to improve our capacity to monitor the SO2 emissions from this volcano. The camera collects images of SO2 concentrations with a period of 10 s, allowing quantification of short-term processes, such as the gas released during the frequent explosions which are synonymous with Stromboli. It also allows quantification of the quiescent gas flux, and therefore comparison with the FLAME network of scanning ultraviolet spectrometers previously installed on the island. Analysis of results from the SO2 camera demonstrated a good agreement with the FLAME network when the plume was blown fully into the field of view of the camera. Permanent volcano monitoring with SO2 cameras is still very much in its infancy, and therefore this finding is a significant step in the use of such cameras for monitoring, whilst also highlighting the requirement of a favourable wind direction and strength. We found that the explosion gas emissions are correlated with seismic events which have a very long period component. There is a variable time lag between event onset time and the increase in gas flux observed by the camera as the explosion gas advects into the field of view of the camera. This variable lag is related to the plume direction, as shown by comparison with the plume location detected with the FLAME network. The correlation between explosion gas emissions and seismic signal amplitude show is consistent with a gas slug-driven mechanism for seismic event production. Comparison of the SO2 camera measurements of the quiescent gas flux shows a fair quantitative agreement with the SO2 flux measured with the FLAME network. Overall, the SO2 camera complements the FLAME network well, as it allows frequent quantification of the explosion gas flux produced by Stromboli, whose signal is in general too brief to be measured with the FLAME network. Further work is required, however, to fully automate the

  18. A new type of iodosulfite ion formulated as I2SO2(2-).

    Science.gov (United States)

    Nagasawa, Isoroku; Amita, Hideaki; Kitagawa, Hiroshi

    2009-01-08

    This paper deals with a notable halosulfite ion, (I2SO2(2-)), which is a rare example of this inorganic anion species; the reaction of the platinum(II) complex, [Pt(depe)2]I2 with SO2 afforded the complex, [Pt(depe)2](I2SO2) containing the rare anion; considering with the VSEPR concept, the structure of the anion could be interpreted as a distorted trigonal bipyramid.

  19. Nanocrystalline BaSnO3 as an Alternative Gas Sensor Material: Surface Reactivity and High Sensitivity to SO2

    Science.gov (United States)

    Marikutsa, Artem; Rumyantseva, Marina; Baranchikov, Alexander; Gaskov, Alexander

    2015-01-01

    Nanocrystalline perovskite-type BaSnO3 was obtained via microwave-assisted hydrothermal route followed by annealing at variable temperature. The samples composition and microstructure were characterized. Particle size of 18–23 nm was unaffected by heat treatment at 275–700 °C. Materials DC-conduction was measured at variable temperature and oxygen concentration. Barium stannate exhibited n-type semiconductor behavior at 150–450 °C with activation energy being dependent on the materials annealing temperature. Predominant ionosorbed oxygen species types were estimated. They were shown to change from molecular to atomic species on increasing temperature. Comparative test of sensor response to various inorganic target gases was performed using nanocrystalline SnO2-based sensors as reference ones. Despite one order of magnitude smaller surface area, BaSnO3 displayed higher sensitivity to SO2 in comparison with SnO2. DRIFT spectroscopy revealed distinct interaction routes of the oxides surfaces with SO2. Barium-promoted sulfate formation favoring target molecules oxidation was found responsible for the increased BaSnO3 sensitivity to ppm-range concentrations of SO2 in air. PMID:28793573

  20. Nanocrystalline BaSnO3 as an Alternative Gas Sensor Material: Surface Reactivity and High Sensitivity to SO2

    Directory of Open Access Journals (Sweden)

    Artem Marikutsa

    2015-09-01

    Full Text Available Nanocrystalline perovskite-type BaSnO3 was obtained via microwave-assisted hydrothermal route followed by annealing at variable temperature. The samples composition and microstructure were characterized. Particle size of 18–23 nm was unaffected by heat treatment at 275–700 °C. Materials DC-conduction was measured at variable temperature and oxygen concentration. Barium stannate exhibited n-type semiconductor behavior at 150–450 °C with activation energy being dependent on the materials annealing temperature. Predominant ionosorbed oxygen species types were estimated. They were shown to change from molecular to atomic species on increasing temperature. Comparative test of sensor response to various inorganic target gases was performed using nanocrystalline SnO2-based sensors as reference ones. Despite one order of magnitude smaller surface area, BaSnO3 displayed higher sensitivity to SO2 in comparison with SnO2. DRIFT spectroscopy revealed distinct interaction routes of the oxides surfaces with SO2. Barium-promoted sulfate formation favoring target molecules oxidation was found responsible for the increased BaSnO3 sensitivity to ppm-range concentrations of SO2 in air.

  1. Aerosol particle charger and an SO2 reactor using energetic electrons

    International Nuclear Information System (INIS)

    Davis, R.H.

    1984-01-01

    Two properties of energetic electrons in gas, their high specific ionization and their production of radicals and other chemically active specie, have promising applications to the cleanup of flue gas from coal combustion. The copious ionization has been used in a test particle charger to electrically charge 1 and 3 μm particles for subsequent removal by electrostatic precipitation. Particle charge greater than 5 times the theoretical ionic charging value for 1 μm particles have been observed in a bi-electrode electron beam precharger in which the beam energy is matched with the electrode spacing. In another test device, pulsed streamer coronas have been used to release and to energize electrons which promote gas phase chemical reactions and remote sulfur dioxide from humid air with high efficiency. The energized electrons produce oxidant radicals and chemically active specie which convert the SO 2 into sulfuric acid mist. While reported separately here, the two applications of energetic electrons may be amenable to combination in an integrated system for the combined treatment of flue gas

  2. Oxygen and SO2Consumption Rates in White and Rosé Wines: Relationship with and Effects on Wine Chemical Composition.

    Science.gov (United States)

    Carrascón, Vanesa; Bueno, Mónica; Fernandez-Zurbano, Purificación; Ferreira, Vicente

    2017-11-01

    This Article addresses the study of O 2 and SO 2 consumption rates of white and rosé wines, their relationship to the initial chemical composition, and their effects on the chemical changes experienced by wine during oxidation. Eight wines were subjected to five consecutive air-saturation cycles. O 2 was monitored periodically; SO 2 , color, and antioxidant indexes were determined after each cycle, and the initial and final compositions of the wines were thoroughly determined. Wines consumed oxygen at progressively decreasing rates. In the last cycles, after a strong decrease, consistent increases of oxygen levels were seen. Oxygen consumption rates were satisfactorily modeled, being proportional to wine copper, quercetin, and kaempherol contents and negatively proportional to cinnamic acids. SO 2 consumption rates were highly diverse between wines and were positively related to free SO 2 , Mn, and pH, among others. In the last saturations, SO 2 consumption took place regardless of O 2 consumption, implying that SO 2 should reduce chemical species oxidized in previous saturations. Some volatile phenols seem to be the end point of radical-mediated oxidation of polyphenols taking place preferably in the first saturation.

  3. OMI measurements of SO2 pollution over Eastern China in 2005-2008

    Science.gov (United States)

    Krotkov, N.; Pickering, K.; Witte, J.; Carn, S.; Yang, K.; Carmichael, G.; Streets, D.; Zhang, Q.; Wei, C.

    2009-05-01

    The Ozone Monitoring Instrument (OMI) on NASA Aura satellite makes global daily measurements of the total column of sulfur dioxide (SO2), a short-lived trace gas produced by fossil fuel combustion, smelting, and volcanoes. OMI seasonal to multi-year average images clearly show the world-highest consistent SO2 pollution in northeast China. China is the world's largest SO2 emitter, mostly due to the burning of high-sulfur coal in its many coal-fired power plants, which lack the technology used in many other countries to remove sulfur from smoke stack emissions. China's government has instituted nationwide measures to control SO2 emissions through the adoption of flue-gas desulfurization technology on new power plants; and even greater measures were adopted in the Beijing area in anticipation of the Olympic Games. To study the environmental effects of the emission controls we compared OMI SO2 time series over eastern China for 2005 through 2008. The time series have been done as 7-day running means of the cloud-free daily observations. By mid-March we started to see substantial periods of lower SO2 values in 2008 compared to 2007, and by mid June the 2008 values were consistently lower than 2007 and prior years. The decline is widespread with highest SO2 typically located to the south and southwest of Beijing in regions with large clusters of power plants and also around Shanghai. The decline also lasted beyond the Olympic season. We do not yet know to what extent the economic downturn in China (and reduced industrial production) contributed to lower SO2 levels in the fall of 2008. We have also compared the observed and modeled fields using University of Iowa STEM model for the period June - September 2008. The model provided SO2 vertical distributions as well as aerosol vertical profiles that were used to correct OMI operational SO2 retrievals and improve the comparisons. The OMI SO2 changes in 2008 have also been compared with the estimated changes in SO2 emissions

  4. Next Generation Aura-OMI SO2 Retrieval Algorithm: Introduction and Implementation Status

    Science.gov (United States)

    Li, Can; Joiner, Joanna; Krotkov, Nickolay A.; Bhartia, Pawan K.

    2014-01-01

    We introduce our next generation algorithm to retrieve SO2 using radiance measurements from the Aura Ozone Monitoring Instrument (OMI). We employ a principal component analysis technique to analyze OMI radiance spectral in 310.5-340 nm acquired over regions with no significant SO2. The resulting principal components (PCs) capture radiance variability caused by both physical processes (e.g., Rayleigh and Raman scattering, and ozone absorption) and measurement artifacts, enabling us to account for these various interferences in SO2 retrievals. By fitting these PCs along with SO2 Jacobians calculated with a radiative transfer model to OMI-measured radiance spectra, we directly estimate SO2 vertical column density in one step. As compared with the previous generation operational OMSO2 PBL (Planetary Boundary Layer) SO2 product, our new algorithm greatly reduces unphysical biases and decreases the noise by a factor of two, providing greater sensitivity to anthropogenic emissions. The new algorithm is fast, eliminates the need for instrument-specific radiance correction schemes, and can be easily adapted to other sensors. These attributes make it a promising technique for producing long-term, consistent SO2 records for air quality and climate research. We have operationally implemented this new algorithm on OMI SIPS for producing the new generation standard OMI SO2 products.

  5. Synthesis of [N(CH3)4]2O3SOSO2(s) and [N(CH3)4]2[(O2SO)2SO2SO2(s) containing (SO4)(SO2)x(2-) x = 1, 2, members of a new class of sulfur oxydianions.

    Science.gov (United States)

    Bruna, Pablo; Decken, Andreas; Grein, Friedrich; Passmore, Jack; Rautiainen, J Mikko; Richardson, Stephanie; Whidden, Tom

    2013-06-17

    One mole equivalent of SO2 reversibly reacts with [N(CH3)4]2SO4(s) to give [N(CH3)4]2S2O6(s) (1) containing the [O3SOSO2](2-), shown by Raman and IR to be an isomer of the [O3SSO3](2-) dianion. The experimental and calculated (B3PW91/6-311+G(3df)) vibrational spectra are in excellent agreement, and the IR spectrum is similar to that of the isoelectronic O3ClOClO2. Crystals of [N(CH3)4]2(O2SO)2SO2·SO2 (2) were isolated from solutions of [N(CH3)4]2SO4 in liquid SO2. The X-ray structure showed that 2 contained the [(O2SO)2SO2](2-) dianion. The characterized N(CH3)4(+) salts 1 and 2 are the first two members of the (SO4)(SO2)x(2-) class of sulfur oxydianions analogous to the well-known small cation salts of the SO4(SO3)x(2-) polysulfates.

  6. Photooxidation of cyclohexene in the presence of SO2: SOA yield and chemical composition

    Science.gov (United States)

    Liu, Shijie; Jia, Long; Xu, Yongfu; Tsona, Narcisse T.; Ge, Shuangshuang; Du, Lin

    2017-11-01

    Secondary organic aerosol (SOA) formation from a cyclohexene / NOx system with various SO2 concentrations under UV light was investigated to study the effects of cyclic alkenes on the atmospheric environment in polluted urban areas. A clear decrease at first and then an increase in the SOA yield was found with increasing SO2 concentrations. The lowest SOA yield was obtained when the initial SO2 concentration was in the range of 30-40 ppb, while higher SOA yield compared to that without SO2 could not be obtained until the initial SO2 concentration was higher than 85 ppb. The decreasing SOA yield might be due to the fact that the promoting effect of acid-catalysed reactions on SOA formation was less important than the inhibiting effect of decreasing OH concentration at low initial SO2 concentrations, caused by the competition reactions of OH with SO2 and cyclohexene. The competitive reaction was an important factor for SOA yield and it should not be neglected in photooxidation reactions. The composition of organic compounds in SOA was measured using several complementary techniques including Fourier transform infrared (FTIR) spectroscopy, ion chromatography (IC), and Exactive Plus Orbitrap mass spectrometer equipped with electrospray interface (ESI). We present new evidence that organosulfates were produced from the photooxidation of cyclohexene in the presence of SO2.

  7. Effect of SO 2 on CO 2 Capture Using Liquid-like Nanoparticle Organic Hybrid Materials

    KAUST Repository

    Lin, Kun-Yi Andrew

    2013-08-15

    Liquid-like nanoparticle organic hybrid materials (NOHMs), consisting of silica nanoparticles with a grafted polymeric canopy, were synthesized. Previous work on NOHMs has revealed that CO2 capture behaviors in these hybrid materials can be tuned by modifying the structure of the polymeric canopy. Because SO2, which is another acidic gas found in flue gas, would also interact with NOHMs, this study was designed to investigate its effect on CO2 capture in NOHMs. In particular, CO2 capture capacities as well as swelling and CO2 packing behaviors of NOHMs were analyzed using thermogravimetric analyses and Raman and attenuated total reflectance (ATR) Fourier transform infrared (FTIR) spectroscopies before and after exposure of NOHMs to SO2. It was found that the SO2 absorption in NOHMs was only prominent at high SO2 levels (i.e., 3010 ppm; Ptot = 0.4 MPa) far exceeding the typical SO2 concentration in flue gas. As expected, the competitive absorption between SO2 and CO2 for the same absorption sites (i.e., ether and amine groups) resulted in a decreased CO2 capture capacity of NOHMs. The swelling of NOHMs was not notably affected by the presence of SO 2 within the given concentration range (Ptot = 0-0.68 MPa). On the other hand, SO2, owing to its Lewis acidic nature, interacted with the ether groups of the polymeric canopy and, thus, changed the CO2 packing behaviors in NOHMs. © 2013 American Chemical Society.

  8. Standard practice for monitoring atmospheric SO2 using the sulfation plate technique

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    1997-01-01

    1.1 This practice covers a weighted average effective SO2 level for a 30-day interval through the use of the sulfation plate method, a technique for estimating the effective SO2 content of the atmosphere, and especially with regard to the atmospheric corrosion of stationary structures or panels. This practice is aimed at determining SO2 levels rather than sulfuric acid aerosol or acid precipitation. 1.2 The results of this practice correlate approximately with volumetric SO2 concentrations, although the presence of dew or condensed moisture tends to enhance the capture of SO2 into the plate. 1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

  9. Integrated assessment of CO2 and SO2 policies in North East Asia

    International Nuclear Information System (INIS)

    Chae, Yeora; Hope, Chris

    2003-01-01

    This study quantifies the costs and impacts of six scenarios for carbon dioxide (CO 2 ) and sulphur dioxide (SO 2 ) emissions in North East Asia (NEA) within an integrated probabilistic analysis. The inclusion of the cooling effect of sulphates means that CO 2 control in China would be likely to increase the regional temperature in NEA in the short-term. This is because CO 2 control measures would also automatically control SO 2 emissions, and so reduce their cooling effect. The scenario that involves no control for CO 2 and SO 2 emissions has the lowest mean total cumulative net present cost (NPC) as compared to scenarios with various SO 2 controls or with CO 2 reduced to 5% below year 1990 levels (in China and Japan), or any combination of SO 2 + CO 2 controls at these levels. The mean value of the total cumulative NPC of climate change damage, acid rain damage, CO 2 and SO 2 control cost in China for no CO 2 or SO 2 control is about US$ 0.1 trillion, compared, for instance, to about US$ 1.1 trillion for CO 2 emission stabilisation at 1990 levels and no SO 2 control. SO 2 control also brings more disadvantages than advantages in China and Japan. The higher mean climate change impacts and control costs outweigh the benefit of lower acid rain damage. However, strict SO 2 control brings more benefits than costs in South Korea where there is a large urban population and the sensitivity to acid rain is high. However, the impacts of emissions and valuation of these effects are very uncertain. Uncertainty analysis shows that the key determinants of the total NPC of costs and damages are exported climate change damages, followed by domestic climate change damages, and acid rain damages. The use of other valuation methods would make health damage bigger than this study's estimation and acid rain damage could be a major concern in the future

  10. A grand canonical Monte Carlo study of SO2 capture using functionalized bilayer graphene nanoribbons

    Science.gov (United States)

    Maurya, Manish; Singh, Jayant K.

    2017-01-01

    Grand canonical Monte Carlo (GCMC) simulation is used to study the adsorption of pure SO2 using a functionalized bilayer graphene nanoribbon (GNR) at 303 K. The functional groups considered in this work are OH, COOH, NH2, NO2, and CH3. The mole percent of functionalization considered in this work is in the range of 3.125%-6.25%. GCMC simulation is further used to study the selective adsorption of SO2 from binary and ternary mixtures of SO2, CO2, and N2, of variable composition using the functionalized bilayer graphene nanoribbon at 303 K. This study shows that the adsorption and selectivity of SO2 increase after the functionalization of the nanoribbon compared to the hydrogen terminated nanoribbon. The order of adsorption capacity and selectivity of the functionalized nanoribbon is found to follow the order COOH > NO2 > NH2 > CH3 > OH > H. The selectivity of SO2 is found to be maximum at a pressure less than 0.2 bar. Furthermore, SO2 selectivity and adsorption capacity decrease with increase in the molar ratio of SO2/N2 mixture from 1:1 to 1:9. In the case of ternary mixture of SO2, CO2, N2, having compositions of 0.05, 0.15, 0.8, the selectivity of SO2 over N2 is higher than that of CO2 over N2. The maximum selectivity of SO2 over CO2 is observed for the COOH functionalized GNR followed by NO2 and other functionalized GNRs.

  11. SO2 plume height retrieval from direct fitting of GOME-2 backscattered radiance measurements

    Science.gov (United States)

    van Gent, J.; Spurr, R.; Theys, N.; Lerot, C.; Brenot, H.; Van Roozendael, M.

    2012-04-01

    The use of satellite measurements for SO2 monitoring has become an important aspect in the support of aviation control. Satellite measurements are sometimes the only information available on SO2 concentrations from volcanic eruption events. The detection of SO2 can furthermore serve as a proxy for the presence of volcanic ash that poses a possible hazard to air traffic. In that respect, knowledge of both the total vertical column amount and the effective altitude of the volcanic SO2 plume is valuable information to air traffic control. The Belgian Institute for Space Aeronomy (BIRA-IASB) hosts the ESA-funded Support to Aviation Control Service (SACS). This system provides Volcanic Ash Advisory Centers (VAACs) worldwide with near real-time SO2 and volcanic ash data, derived from measurements from space. We present results from our algorithm for the simultaneous retrieval of total vertical columns of O3 and SO2 and effective SO2 plume height from GOME-2 backscattered radiance measurements. The algorithm is an extension to the GODFIT direct fitting algorithm, initially developed at BIRA-IASB for the derivation of improved total ozone columns from satellite data. The algorithm uses parameterized vertical SO2 profiles which allow for the derivation of the peak height of the SO2 plume, along with the trace gas total column amounts. To illustrate the applicability of the method, we present three case studies on recent volcanic eruptions: Merapi (2010), Grímsvotn (2011), and Nabro (2011). The derived SO2 plume altitude values are validated with the trajectory model FLEXPART and with aerosol altitude estimations from the CALIOP instrument on-board the NASA A-train CALIPSO platform. We find that the effective plume height can be obtained with a precision as fine as 1 km for moderate and strong volcanic events. Since this is valuable information for air traffic, we aim at incorporating the plume height information in the SACS system.

  12. New approaches to merging multi-sensor satellite measurements of volcanic SO2 emissions

    Science.gov (United States)

    Carn, S. A.; Telling, J. W.; Krotkov, N. A.

    2015-12-01

    As part of the NASA MEaSUREs program, we are developing a unique long-term database of volcanic sulfur dioxide (SO2) emissions for use by the scientific community, using observations from multiple satellite instruments collected since 1978. Challenges to creating such a database include assessing data continuity between multiple satellite missions and SO2 retrieval algorithms and estimating measurement uncertainties. Here, we describe the approaches that we are using to merge multi-decadal SO2 measurements from the ultraviolet (UV) Total Ozone Mapping Spectrometer (TOMS), Ozone Monitoring Instrument (OMI) and Ozone Monitoring and Profiler Suite (OMPS) sensors. A particular challenge has involved accounting for the OMI row anomaly (ORA), a data gap in OMI measurements since 2008 that partially or wholly obscures some volcanic eruption clouds, whilst still profiting from the high OMI spatial resolution and data quality, and prior OMI SO2 validation. We present a new method to substitute missing SO2 information in the ORA with near-coincident SO2 data from OMPS, providing improved estimates of eruptive volcanic SO2 emissions. The technique can also be used to assess consistency between different satellite instruments and SO2 retrieval algorithms, investigate the impact of variable sensor spatial resolution, and estimate measurement uncertainties. It is particularly effective for larger eruptions producing extensive SO2 clouds where the ORA obscures the volcanic plume in multiple contiguous orbits. Application of the technique is demonstrated using recent volcanic eruptions including the 2015 eruption of Calbuco, Chile. We also provide an update on the status of the multi-satellite long-term volcanic SO2 database (MSVOLSO2L4).

  13. Intercomparison of SO2 camera systems for imaging volcanic gas plumes

    Science.gov (United States)

    Kern, Christoph; Lübcke, Peter; Bobrowski, Nicole; Campion, Robin; Mori, Toshiya; Smekens, Jean-François; Stebel, Kerstin; Tamburello, Giancarlo; Burton, Mike; Platt, Ulrich; Prata, Fred

    2015-07-01

    SO2 camera systems are increasingly being used to image volcanic gas plumes. The ability to derive SO2 emission rates directly from the acquired imagery at high time resolution allows volcanic process studies that incorporate other high time-resolution datasets. Though the general principles behind the SO2 camera have remained the same for a number of years, recent advances in CCD technology and an improved understanding of the physics behind the measurements have driven a continuous evolution of the camera systems. Here we present an intercomparison of seven different SO2 cameras. In the first part of the experiment, the various technical designs are compared and the advantages and drawbacks of individual design options are considered. Though the ideal design was found to be dependent on the specific application, a number of general recommendations are made. Next, a time series of images recorded by all instruments at Stromboli Volcano (Italy) is compared. All instruments were easily able to capture SO2 clouds emitted from the summit vents. Quantitative comparison of the SO2 load in an individual cloud yielded an intra-instrument precision of about 12%. From the imagery, emission rates were then derived according to each group's standard retrieval process. A daily average SO2 emission rate of 61 ± 10 t/d was calculated. Due to differences in spatial integration methods and plume velocity determination, the time-dependent progression of SO2 emissions varied significantly among the individual systems. However, integration over distinct degassing events yielded comparable SO2 masses. Based on the intercomparison data, we find an approximate 1-sigma precision of 20% for the emission rates derived from the various SO2 cameras. Though it may still be improved in the future, this is currently within the typical accuracy of the measurement and is considered sufficient for most applications.

  14. The physico-chemistry of SO2 in the smoke plumes of fossil-fueled power plants

    International Nuclear Information System (INIS)

    Sabroux, Jean-Christophe

    1974-01-01

    An experimental determination was made of the type and speed of chemical-physical transformations occurring in the stack effluents of fossil-fueled power-plants, from their emission into the atmosphere. The homogeneous chemical reactions were taken into consideration, as well as the heterogeneous reactions in the presence of a metal, oxide aerosol or water droplets owed to condensation. The results gave a general indication that the quantitatively important transformations of SO 2 , in a stack plume produced by fuel combustion, took place at the moment of water-vapor condensation; in these conditions the oxidising role of NO 2 became prevailing. (author) [fr

  15. Formation of Nanodroplets in N2/H2O/SO2 under Irradiation of Fast Proton Beams

    DEFF Research Database (Denmark)

    Nakai, Youchi; Shigeoka, Tomita; Funada, Shuhei

    The droplet formation induced by cosmic ray in the terrestrial atmosphere attract certainattention in recent decades because this process could be important to understand thepossible relationship between cosmic ray and climate on the earth. The role of energetic ionsfor the droplet formation would...... measured with adifferential mobility analyzer. We found that the mass yield of generated droplets showedlinear dependence on the amount of SO2 oxidation. This behavior is different from binarynucleation theory of water and H2SO4. The difference might indicates importance ofconsidering the droplet formation...

  16. Sulfur dioxide (SO2) vertical column density measurements by Pandora spectrometer over the Canadian oil sands

    Science.gov (United States)

    Fioletov, Vitali E.; McLinden, Chris A.; Cede, Alexander; Davies, Jonathan; Mihele, Cristian; Netcheva, Stoyka; Li, Shao-Meng; O'Brien, Jason

    2016-07-01

    Vertical column densities (VCDs) of SO2 retrieved by a Pandora spectral sun photometer at Fort McKay, Alberta, Canada, from 2013 to 2015 were analysed. The Fort McKay site is located in the Canadian oil sands region, approximately 20 km north of two major SO2 sources (upgraders), with total emission of about 45 kt yr-1. Elevated SO2 VCD values were frequently recorded by the instrument, with the highest values of about 9 Dobson Units (DU; DU = 2.69 × 1016 molecules cm-2). Comparisons with co-located in situ measurements demonstrated that there was a very good correlation between VCDs and surface concentrations in some cases, while in other cases, elevated VCDs did not correspond to high surface concentrations, suggesting the plume was above the ground. Elevated VCDs and surface concentrations were observed when the wind direction was from south to southeast, i.e. from the direction of the two local SO2 sources. The precision of the SO2 measurements, estimated from parallel measurements by two Pandora instruments at Toronto, is 0.17 DU. The total uncertainty of Pandora SO2 VCD, estimated using measurements when the wind direction was away from the sources, is less than 0.26 DU (1σ). Comparisons with integrated SO2 profiles from concurrent aircraft measurements support these estimates.

  17. A decade of global volcanic SO2 emissions measured from space

    Science.gov (United States)

    Carn, S. A.; Fioletov, V. E.; McLinden, C. A.; Li, C.; Krotkov, N. A.

    2017-03-01

    The global flux of sulfur dioxide (SO2) emitted by passive volcanic degassing is a key parameter that constrains the fluxes of other volcanic gases (including carbon dioxide, CO2) and toxic trace metals (e.g., mercury). It is also a required input for atmospheric chemistry and climate models, since it impacts the tropospheric burden of sulfate aerosol, a major climate-forcing species. Despite its significance, an inventory of passive volcanic degassing is very difficult to produce, due largely to the patchy spatial and temporal coverage of ground-based SO2 measurements. We report here the first volcanic SO2 emissions inventory derived from global, coincident satellite measurements, made by the Ozone Monitoring Instrument (OMI) on NASA’s Aura satellite in 2005-2015. The OMI measurements permit estimation of SO2 emissions from over 90 volcanoes, including new constraints on fluxes from Indonesia, Papua New Guinea, the Aleutian Islands, the Kuril Islands and Kamchatka. On average over the past decade, the volcanic SO2 sources consistently detected from space have discharged a total of ~63 kt/day SO2 during passive degassing, or ~23 ± 2 Tg/yr. We find that ~30% of the sources show significant decadal trends in SO2 emissions, with positive trends observed at multiple volcanoes in some regions including Vanuatu, southern Japan, Peru and Chile.

  18. A decade of global volcanic SO2 emissions measured from space

    Science.gov (United States)

    Carn, S. A.; Fioletov, V. E.; McLinden, C. A.; Li, C.; Krotkov, N. A.

    2017-01-01

    The global flux of sulfur dioxide (SO2) emitted by passive volcanic degassing is a key parameter that constrains the fluxes of other volcanic gases (including carbon dioxide, CO2) and toxic trace metals (e.g., mercury). It is also a required input for atmospheric chemistry and climate models, since it impacts the tropospheric burden of sulfate aerosol, a major climate-forcing species. Despite its significance, an inventory of passive volcanic degassing is very difficult to produce, due largely to the patchy spatial and temporal coverage of ground-based SO2 measurements. We report here the first volcanic SO2 emissions inventory derived from global, coincident satellite measurements, made by the Ozone Monitoring Instrument (OMI) on NASA’s Aura satellite in 2005–2015. The OMI measurements permit estimation of SO2 emissions from over 90 volcanoes, including new constraints on fluxes from Indonesia, Papua New Guinea, the Aleutian Islands, the Kuril Islands and Kamchatka. On average over the past decade, the volcanic SO2 sources consistently detected from space have discharged a total of ~63 kt/day SO2 during passive degassing, or ~23 ± 2 Tg/yr. We find that ~30% of the sources show significant decadal trends in SO2 emissions, with positive trends observed at multiple volcanoes in some regions including Vanuatu, southern Japan, Peru and Chile. PMID:28275238

  19. Extended SO2 outgassing from the 2014-2015 Holuhraun lava flow field, Iceland

    Science.gov (United States)

    Simmons, Isla C.; Pfeffer, Melissa A.; Calder, Eliza S.; Galle, Bo; Arellano, Santiago; Coppola, Diego; Barsotti, Sara

    2017-11-01

    The 2014-2015 Holuhraun eruption was the largest fissure eruption in Iceland in the last 200 years. This flood basalt eruption produced 1.6 km3 of lava, forming a lava flow field covering an area of 84 km2. Over the 6-month course of the eruption, 11 Mt of SO2 were released from the eruptive vents as well as from the cooling lava flow field. This work examines the post-eruption SO2 flux emitted by the Holuhraun lava flow field, providing the first study of the extent and relative importance of the outgassing of a lava flow field after emplacement. We use data from a scanning differential optical absorption spectroscopy (DOAS) instrument installed at the eruption site to monitor the flux of SO2. In this study, we propose a new method to estimate the SO2 emissions from the lava flow field, based on the characteristic shape of the scanned column density distribution of a homogenous source close to the ground. Post-eruption outgassing of the lava flow field continued for at least 3 months after the end of the eruption, with SO2 flux between < 1 and 9 kg/s. The lava flow field post-eruption emissions were not a significant contributor to the total SO2 released during the eruption; however, the lava flow field was still an important polluter and caused high concentrations of SO2 at ground level after lava effusion ceased.

  20. A decade of global volcanic SO2emissions measured from space.

    Science.gov (United States)

    Carn, S A; Fioletov, V E; McLinden, C A; Li, C; Krotkov, N A

    2017-03-09

    The global flux of sulfur dioxide (SO 2 ) emitted by passive volcanic degassing is a key parameter that constrains the fluxes of other volcanic gases (including carbon dioxide, CO 2 ) and toxic trace metals (e.g., mercury). It is also a required input for atmospheric chemistry and climate models, since it impacts the tropospheric burden of sulfate aerosol, a major climate-forcing species. Despite its significance, an inventory of passive volcanic degassing is very difficult to produce, due largely to the patchy spatial and temporal coverage of ground-based SO 2 measurements. We report here the first volcanic SO 2 emissions inventory derived from global, coincident satellite measurements, made by the Ozone Monitoring Instrument (OMI) on NASA's Aura satellite in 2005-2015. The OMI measurements permit estimation of SO 2 emissions from over 90 volcanoes, including new constraints on fluxes from Indonesia, Papua New Guinea, the Aleutian Islands, the Kuril Islands and Kamchatka. On average over the past decade, the volcanic SO 2 sources consistently detected from space have discharged a total of ~63 kt/day SO 2 during passive degassing, or ~23 ± 2 Tg/yr. We find that ~30% of the sources show significant decadal trends in SO 2 emissions, with positive trends observed at multiple volcanoes in some regions including Vanuatu, southern Japan, Peru and Chile.

  1. SO2 columns over China: Temporal and spatial variations using OMI and GOME-2 observations

    International Nuclear Information System (INIS)

    Huanhuan, Yan; Liangfu, Chen; Lin, Su; Jinhua, Tao; Chao, Yu

    2014-01-01

    Enhancements of SO 2 column amounts due to anthropogenic emission sources over China were shown in this paper by using OMI and GOME-2 observations. The temporal and spatial variations of SO 2 columns over China were analyzed for the time period 2005–2010. Beijing and Chongqing showed a high concentration in the SO 2 columns, attributable to the use of coal for power generation in China and the characteristic of terrain and meteorology. The reduction of SO 2 columns over Beijing and surrounding provinces in 2008 was observed by OMI, which confirms the effectiveness of strict controls on pollutant emissions and motor vehicle traffic before and during 2008 Olympic and Paralympic Games. The SO 2 columns over China from GOME-2 (0.2–0.5 DU) were lower than those from OMI (0.6–1 DU), but both showed a decrease in SO 2 columns over northern China since 2008 (except an increase in OMI SO 2 in 2010)

  2. Changes in SO2 and NO2 Pollution over the Past Decade Observed by Aura OMI

    Science.gov (United States)

    Krotkov, N. A.; Li, C.; Lamsal, L. N.; Celarier, E. A.; Marchenko, S. V.; Swartz, W.; Bucsela, E. J.; Fioletov, V.; McLinden, C. A.; Joiner, J.; Bhartia, P. K.; Duncan, B. N.; Dickerson, R. R.

    2014-12-01

    The Ozone Monitoring Instrument (OMI), a NASA partnership with the Netherlands and Finland, flies on the EOS Aura satellite and uses reflected sunlight to measure two critical atmospheric trace gases, nitrogen dioxide (NO2) and sulfur dioxide (SO2), characterizing daily air quality. Both gases and the secondary pollutants they produce (particulate matter, PM2.5, and tropospheric ozone) are among USEPA designated criteria pollutants, posing serious threats to human health and the environment (e.g., acid rain, plant damage, and reduced visibility). A new generation of the OMI standard SO2 and NO2 products (based on critically improved DOAS spectral fitting for NO2 and innovative Principal Component Analysis method for SO2) provides a valuable dataset for studying anthropogenic pollution on local to global scales. Here we highlight some of the OMI observed long-term changes in air quality over several regions. Over the US, average NO2 and SO2 pollution levels have decreased dramatically as a result of both technological improvements (e.g., catalytic converters on cars) and stricter regulations of emissions. We see continued decline in NO2 and SO2 pollution over Europe. Over China OMI observed a ~ 60% increase in NO2 pollution between 2005 and 2013, despite a temporary reversal of the growing trend due to both 2008 Olympic Games and the economic recession in 2009. Chinese SO2 pollution seems to have stabilized since peaking in 2007, probably due to government efforts to curb SO2 emissions from the power sector. We have also observed large increases in both SO2 and NO2 pollution particularly in Eastern India where a number of new large coal power plants have been built in recent years. We expect that further improvements in the OMI NO2 and SO2 products will allow more robust quantification of long-term trends in local to global air quality.

  3. Lessons Learned from OMI Observations of Point Source SO2 Pollution

    Science.gov (United States)

    Krotkov, N.; Fioletov, V.; McLinden, Chris

    2011-01-01

    The Ozone Monitoring Instrument (OMI) on NASA Aura satellite makes global daily measurements of the total column of sulfur dioxide (SO2), a short-lived trace gas produced by fossil fuel combustion, smelting, and volcanoes. Although anthropogenic SO2 signals may not be detectable in a single OMI pixel, it is possible to see the source and determine its exact location by averaging a large number of individual measurements. We describe new techniques for spatial and temporal averaging that have been applied to the OMI SO2 data to determine the spatial distributions or "fingerprints" of SO2 burdens from top 100 pollution sources in North America. The technique requires averaging of several years of OMI daily measurements to observe SO2 pollution from typical anthropogenic sources. We found that the largest point sources of SO2 in the U.S. produce elevated SO2 values over a relatively small area - within 20-30 km radius. Therefore, one needs higher than OMI spatial resolution to monitor typical SO2 sources. TROPOMI instrument on the ESA Sentinel 5 precursor mission will have improved ground resolution (approximately 7 km at nadir), but is limited to once a day measurement. A pointable geostationary UVB spectrometer with variable spatial resolution and flexible sampling frequency could potentially achieve the goal of daily monitoring of SO2 point sources and resolve downwind plumes. This concept of taking the measurements at high frequency to enhance weak signals needs to be demonstrated with a GEOCAPE precursor mission before 2020, which will help formulating GEOCAPE measurement requirements.

  4. Application of V2O5/WO3/TiO2 for Resistive-Type SO2 Sensors

    Directory of Open Access Journals (Sweden)

    Ralf Moos

    2011-03-01

    Full Text Available A study on the application of V2O5/WO3/TiO2 (VWT as the sensitive material for resistive-type SO2 sensor was conducted, based on the fact that VWT is a well-known catalyst material for good selective catalytic nitrogen oxide reduction with a proven excellent durability in exhaust gases. The sensors fabricated in this study are planar ones with interdigitated electrodes of Au or Pt. The vanadium content of the utilized VWT is 1.5 or 3.0 wt%. The resistance of VWT decreases with an increasing SO2 concentration in the range from 20 ppm to 5,000 ppm. The best sensor response to SO2 occurs at 400 °C using Au electrodes. The sensor response value is independent on the amount of added vanadium but dependent on the electrode materials at 400 °C. These results are discussed and a sensing mechanism is discussed.

  5. Response of Calendula officinalis L. to long-term fumigation with SO2

    Energy Technology Data Exchange (ETDEWEB)

    Singh, S.N.; Yunus, M.; Srivastava, K.; Kulshreshtha, K.; Ahmad, K.J.

    1985-01-01

    Seedlings of Calendula officinalis L. (30-days old) were raised in 1 mS plots and fumigated with 1 and 2 g liter SO2 on alternate days. Analysis of plant samples collected at pre-flowering, flowering and post-flowering stages showed that photosynthetic pigments were degraded and leaf extract pH and protein content declined in SO2 treated plants. In addition, scanning electron microscopic studies revealed that SO2 stimulated the widening of stomatal pores in fumigated plants.

  6. SO2 emissions from paroxysmal eruptions at Etna volcano in 2011-12

    Science.gov (United States)

    Bonny, E.; Mandon, C.; Carn, S. A.; Prata, F.; Coltelli, M.; Donnadieu, F.

    2013-12-01

    Mt Etna's activity has increased during the last decade with a tendency towards more explosive eruptions that produce paroxysmal lava fountains. From January 2011 to April 2012, 25 lava fountaining episodes took place at Etna's New South-East Crater (NSEC). Improved understanding of the mechanism driving these explosive basaltic eruptions is needed to reduce volcanic hazards and develop models of Etna's plumbing system.. This type of activity produces high sulfur dioxide (SO2) emissions, associated with lava flows and ash fall-out, but to date the SO2 emissions associated with Etna's lava fountains have been poorly constrained. The Ultraviolet (UV) Ozone Monitoring Instrument (OMI) on NASA's Aura satellite and the Atmospheric Infrared Sounder (AIRS) on Aqua were used to measure the SO2 loadings. Ground-based data from the Observatoire de Physique du Globe de Clermont-Ferrand (OPGC) L-band Doppler radar, VOLDORAD 2B, used in collaboration with the Italian National Institute of Geophysics and Volcanology in Catania (INGV-CT), also detected the associated ash plumes, giving precise timing and duration for the lava fountains. This study resulted in the first detailed analysis of the OMI and AIRS SO2 data for Etna's lava fountains during the 2011-2012 eruptive cycle. The HYSPLIT trajectory model is used to constrain the altitude of the observed SO2 clouds, and results show that the SO2 emission usually coincided with the lava fountain peak intensity as detected by VOLDORAD. The UV OMI and IR AIRS SO2 retrievals permit quantification of the SO2 loss rate in the volcanic SO2 clouds, many of which were tracked for several days after emission. Using SO2 loadings corrected for the time of emission, we observe a correlation between SO2 production and inter-paroxysm repose time, suggesting that gas accumulation drives the paroxysms. We therefore suggest that our data set supports the collapsing foam (CF) model [Parfitt (2004) J. Volcanol. Geotherm. Res. 134, 77-107.] as the

  7. The global distribution, abundance, and stability of SO2 on Io

    Science.gov (United States)

    McEwen, A.S.; Johnson, T.V.; Matson, D.L.; Soderblom, L.A.

    1988-01-01

    Sulfur dioxide distribution and abundances, bolometric hemispheric albedos, and passive surface temperatures on Io are modeled and mapped globally from Voyager multispectral mosaics, Earth-based spectra, and photometric descriptions. Photometric models indicate global average values for regolith porosity of 75-95% and macroscopic roughness with a mean slope angle of ~30??. Abundances of SO2 suggested by observations at uv-visible wavelengths and at 4.08 ??m are partially reconciled by intimate-mixing models; 30-50% SO2 coverage of the integral disk is indicated. Three major spectral end members, with continuous mixing, are recognized from the Voyager multispectral mosaics; one of these end members is identified as SO2. Intimate-mixing models with the three spectal end members are used to produce abundance maps for the optical surface; ~30% of Io's total optical surface consists of SO2. The SO2 is concentrated in the bright equatorial band and is relatively deficient in the region of Pele-type volcanic reuptions (long 240??-360??) and the polar regions. Temperatures are computed to vary over a 40??K range, at the same illumination angle, according to variations in surface bolometric hemispheric albedo. The brightest (and locally coldest) areas correspond to areas rich in SO2 and are concentrated in an equatorial band (??30?? lat), but many small cold patches occur elsewhere. These cold patches have radiative equilibrium temperatures ???120??K at the subsolar point, resulting in SO2 saturation vapor pressures ???10-8 bar. Midlatitude areas and the region of Pele-type plume eruptions are generally warmer (due to lower albedos). These results for surface temperatures and SO2 abundances and distribution support the regional coldtrapping model for the surface and atmospheric SO2 presented by F.P. Fanale, W.B. Banerdt, L.S. Elson, T.V. Johnson, and R.W. Zurek (1982, In Satellites of Jupiter (D. Morrison, Ed.), pp. 756-781, Univ. of Arizona Press, Tucson), although the

  8. A Green Desulfurization Technique: Utilization of Flue Gas SO2 to Produce H2 via a Photoelectrochemical Process Based on Mo-Doped BiVO4

    Directory of Open Access Journals (Sweden)

    Jin Han

    2017-12-01

    Full Text Available A green photoelectrochemical (PEC process with simultaneous SO2 removal and H2 production has attracted an increasing attention. The proposed process uses flue gas SO2 to improve H2 production. The improvement of the efficiency of this process is necessary before it can become industrial viable. Herein, we reported a Mo modified BiVO4 photocatalysts for a simultaneous SO2 removal and H2 production. And the PEC performance could be significantly improved with doping and flue gas removal. The evolution rate of H2 and removal of SO2 could be enhanced by almost three times after Mo doping as compared with pristine BiVO4. The enhanced H2 production and SO2 removal is attributed to the improved bulk charge carrier transportation after Mo doping, and greatly enhanced oxidation reaction kinetics on the photoanode due to the formation of SO32− after SO2 absorption by the electrolyte. Due to the utilization of SO2 to improve the production of H2, the proposed PEC process may become a profitable desulfurization technique.

  9. Lost in Cloud

    Science.gov (United States)

    Maluf, David A.; Shetye, Sandeep D.; Chilukuri, Sri; Sturken, Ian

    2012-01-01

    Cloud computing can reduce cost significantly because businesses can share computing resources. In recent years Small and Medium Businesses (SMB) have used Cloud effectively for cost saving and for sharing IT expenses. With the success of SMBs, many perceive that the larger enterprises ought to move into Cloud environment as well. Government agency s stove-piped environments are being considered as candidates for potential use of Cloud either as an enterprise entity or pockets of small communities. Cloud Computing is the delivery of computing as a service rather than as a product, whereby shared resources, software, and information are provided to computers and other devices as a utility over a network. Underneath the offered services, there exists a modern infrastructure cost of which is often spread across its services or its investors. As NASA is considered as an Enterprise class organization, like other enterprises, a shift has been occurring in perceiving its IT services as candidates for Cloud services. This paper discusses market trends in cloud computing from an enterprise angle and then addresses the topic of Cloud Computing for NASA in two possible forms. First, in the form of a public Cloud to support it as an enterprise, as well as to share it with the commercial and public at large. Second, as a private Cloud wherein the infrastructure is operated solely for NASA, whether managed internally or by a third-party and hosted internally or externally. The paper addresses the strengths and weaknesses of both paradigms of public and private Clouds, in both internally and externally operated settings. The content of the paper is from a NASA perspective but is applicable to any large enterprise with thousands of employees and contractors.

  10. Multi-decadal satellite measurements of passive and eruptive volcanic SO2 emissions

    Science.gov (United States)

    Carn, Simon; Yang, Kai; Krotkov, Nickolay; Prata, Fred; Telling, Jennifer

    2015-04-01

    Periodic injections of sulfur gas species (SO2, H2S) into the stratosphere by volcanic eruptions are among the most important, and yet unpredictable, drivers of natural climate variability. However, passive (lower tropospheric) volcanic degassing is the major component of total volcanic emissions to the atmosphere on a time-averaged basis, but is poorly constrained, impacting estimates of global emissions of other volcanic gases (e.g., CO2). Stratospheric volcanic emissions are very well quantified by satellite remote sensing techniques, and we report ongoing efforts to catalog all significant volcanic SO2 emissions into the stratosphere and troposphere since 1978 using measurements from the ultraviolet (UV) Total Ozone Mapping Spectrometer (TOMS; 1978-2005), Ozone Monitoring Instrument (OMI; 2004 - present) and Ozone Mapping and Profiler Suite (OMPS; 2012 - present) instruments, supplemented by infrared (IR) data from HIRS, MODIS and AIRS. The database, intended for use as a volcanic forcing dataset in climate models, currently includes over 600 eruptions releasing a total of ~100 Tg SO2, with a mean eruption discharge of ~0.2 Tg SO2. Sensitivity to SO2 emissions from smaller eruptions greatly increased following the launch of OMI in 2004, but uncertainties remain on the volcanic flux of other sulfur species other than SO2 (H2S, OCS) due to difficulty of measurement. Although the post-Pinatubo 1991 era is often classified as volcanically quiescent, many smaller eruptions (Volcanic Explosivity Index [VEI] 3-4) since 2000 have injected significant amounts of SO2 into the upper troposphere - lower stratosphere (UTLS), peaking in 2008-2011. We also show how even smaller (VEI 2) tropical eruptions can impact the UTLS and sustain above-background stratospheric aerosol optical depth, thus playing a role in climate forcing on short timescales. To better quantify tropospheric volcanic degassing, we use ~10 years of operational SO2 measurements by OMI to identify the

  11. Decadal-scale joint inversion of NOx and SO2 using a hybrid 4D-Var / mass balance approach

    Science.gov (United States)

    Qu, Z.; Henze, D. K.; Capps, S.; Wang, Y.; Xu, X.; Wang, J.; Keller, M.

    2016-12-01

    Quantifying the emissions of nitrogen oxides (NOx) and sulfur dioxide (SO2) is important for improving our understanding of acid rain, formation of aerosols, and human health problems. Traditional top-down estimates have provided valuable constraints for NOx and SO2 emission inventories in China, but are either time-consuming (e.g., 4D-Var) or only crudely represent the influence of atmospheric transport and chemistry (e.g., mass balance). We develop an approach combining mass balance and an adjoint-based four-dimensional variational (4D-Var) methods that facilitates decadal-scale emission inversions. This hybrid inversion is first evaluated with a single species inversion using NO2 pseudo observations. In a set of seven-year pseudo observation test, hybrid posterior NOx emissions have smaller normalized mean square error (by 54% to 94%) than that of mass balance when compared to true emissions in most cases, and have slightly better performance in detecting emissions magnitudes and trends. Using this hybrid method, NO2 observations from the Ozone Monitoring Instrument (OMI), and the GEOS-Chem chemical transport model, we have derived monthly top-down NOx emissions for China from 2005 to 2012. Our posterior emissions have the same seasonality as recent bottom-up inventories, and smaller emissions (by 13.4% to 23.5%) as well as emission growth rate (by 0.6% to 4.1%). The hybrid method is further implemented for long-term joint inversion of NOx and SO2 emissions in China using combined observations of OMI NO2 and SO2 column densities. A 4D-Var inversion is first performed to optimize NOx and SO2 emissions in the base year using GEOS-Chem adjoint. Mass balance scaling factor is then applied to these posterior to improve their inter-annual variation. Overall, these studies augment the utility of remote sensing data for evaluating emission control strategies and mitigating the impact of NOx and SO2 on human health and the environment.

  12. Protective performances of two anti-graffiti treatments towards sulfite and sulfate formation in SO 2 polluted model environment

    Science.gov (United States)

    Carmona-Quiroga, Paula María; Panas, Itai; Svensson, Jan-Erik; Johansson, Lars-Gunnar; Blanco-Varela, María Teresa; Martínez-Ramírez, Sagrario

    2010-11-01

    Specific strategies for protection are being developed to counter both the staining and corrosive effects of polluted air in cities, as well as to allow for efficient removal of unwanted graffiti paintings. These protection strategies employ molecules with tailored functionalities, e.g. being hydrophobic, while maintaining porosity for molecular water vapour permeation. The present study employs SO 2 and water to probe the behaviors of two anti-graffiti treatments, a water-base fluoroalkylsiloxane ("Protectosil Antigraffiti" marketed by Degussa) and an organically modified silicate (Ormosil) synthesized from a polymer chain (polydimethyl siloxane, PDMS) and two network forming alkoxides (Zr propoxide and methyl triethoxy silane, MTES) dissolved in n-propanol, on five building materials, comprising limestone, aged lime mortar, hydrated cement mortar, granite, and brick material. The materials were exposed to a synthetic atmosphere for 20 h in a climate chamber, 0.78 ± 0.03 ppm of SO 2 and 95% RH. Diffuse reflectance Fourier transform infrared (DR-FTIR) spectra were registered before and after exposure in the climate chamber in the cases of both treated and untreated samples. DR-FTIR, scanning electron microscope (SEM) images and energy dispersive X-ray (EDX) analyses, suggest the anti-graffiti Ormosil to suppress formation of calcium sulfite hemihydrate (the primary initial product of the reaction of calcium compounds with SO 2 and water) on carbonate materials (limestone and lime mortar). In case of the granite, brick and cement mortar, Ormosil has a negligible influence on the SO 2 capture. While no sulfite formation was detected by DR-FTIR, gypsum is inferred to form due to metal oxides and minority compounds catalysed oxidation of sulfite to sulfate. In case of brick, this understanding finds support from SEM images as well as EDX. A priori presence of gypsum in hydrated cement mortars prevents positive identification by SEM. However, support for sulfur

  13. Airborne multi-axis DOAS measurements of tropospheric SO2 plumes in the Po-valley, Italy

    Directory of Open Access Journals (Sweden)

    P. Wang

    2006-01-01

    Full Text Available During the second FORMAT (FORMaldehyde as A Tracer of oxidation in the troposphere campaign in 2003 the airborne multi-axis DOAS instrument (AMAXDOAS performed scattered-light spectroscopic measurements of SO2 over the city of Mantova and the power plant Porto Tolle, both situated in the Po-valley, Northern Italy. The SO2 vertical columns and emission flux were derived from two days of measurements, 26 and 27 September 2003. The SO2 emission flux from the power plant Porto Tolle was calculated to 1.93×1025 molec s-1 on 26 September and in good agreement with official emission data, which quote 2.25×1025 molec s-1. On 27 September the measured flux was much lower (3.77×1024 molec s-1 if ECMWF wind data are used, but of comparable magnitude (2.4×1025 molec s-1 if the aircraft on-board wind measurements are utilised. Official emission data was 2.07×1025 molec s-1 indicating only a small change from the previous day. Over the city of Mantova, the observed SO2 vertical columns were 1.1×1016 molec cm-2 and 1.9×1016 molec cm-2 on 26 and 27 September, respectively. This is in good agreement with ground-based measurements of 5.9 ppbv and 10.0 ppbv which correspond to 1.2×1016 molec cm-2 and 2.2×1016 molec cm-2 if a well mixed boundary layer of 500m altitude is assumed.

  14. Mineral dust and NOx promote the conversion of SO2 to sulfate in heavy pollution days.

    Science.gov (United States)

    He, Hong; Wang, Yuesi; Ma, Qingxin; Ma, Jinzhu; Chu, Biwu; Ji, Dongsheng; Tang, Guiqian; Liu, Chang; Zhang, Hongxing; Hao, Jiming

    2014-02-25

    Haze in China has been increasing in frequency of occurrence as well as the area of the affected region. Here, we report on a new mechanism of haze formation, in which coexistence with NOx can reduce the environmental capacity for SO2, leading to rapid conversion of SO2 to sulfate because NO2 and SO2 have a synergistic effect when they react on the surface of mineral dust. Monitoring data from five severe haze episodes in January of 2013 in the Beijing-Tianjin-Hebei regions agreed very well with the laboratory simulation. The combined air pollution of motor vehicle exhaust and coal-fired flue gases greatly reduced the atmospheric environmental capacity for SO2, and the formation of sulfate was found to be a main reason for the growth of fine particles, which led to the occurrence of haze. These results indicate that the impact of motor vehicle exhaust on the atmospheric environment might be underestimated.

  15. Adsorption behavior of SO2 on vacancy-defected graphene: A DFT study

    Science.gov (United States)

    Zhou, Qingxiao; Ju, Weiwei; Su, Xiangying; Yong, Yongliang; Li, Xiaohong

    2017-10-01

    The adsorption of an SO2 molecule on the perfect and point-defective graphene surfaces were investigated using density functional theory (DFT). The geometric structure, adsorption energy, charge transfer, and electronic properties were calculated and analyzed to characterize the effect of vacancy on the adsorption process of SO2 on the graphene. The result indicated that the presence of vacancy enhanced the adsorption stability with the larger adsorption energy and net charge transfer compared to that of perfect graphene. Moreover, the SO2 molecule on different adsorption sites exhibited dissimilar states because of the adsorption. Furthermore, the results of the electronic properties revealed that the adsorption of SO2 induced an opening of the band gap.

  16. US EPA Nonattainment Areas and Designations-SO2 (2010 NAAQS)

    Data.gov (United States)

    U.S. Environmental Protection Agency — This web service contains the following layer: SO2 2010 NAAQS State Level. Full FGDC metadata records for each layer may be found by clicking the layer name at the...

  17. MLS/Aura L2 Sulfur Dioxide (SO2) Mixing Ratio V003

    Data.gov (United States)

    National Aeronautics and Space Administration — ML2SO2 is the EOS Aura Microwave Limb Sounder (MLS) standard product for sulfur dioxide derived from radiances measured by the 240 GHz radiometer. The current...

  18. Combined treatment of SO2 and high resistivity fly ash using a pulse energized electron reactor

    International Nuclear Information System (INIS)

    Mizuno, A.; Clements, J.S.; Davis, R.H.

    1984-01-01

    The combined removal of SO 2 and high resistivity fly ash has been demonstrated in a pulse energized electron reactor (PEER). The PEER system which was originally developed for the removal of SO 2 utilizes a positive pulse streamer corona discharge in a non-uniform field geometry. In performance tests on SO 2 , more than 90% was removed with an advantageously small power requirement. Combined treatment performance was demonstrated by introducing high resistivity fly ash into the test gas and the PEER is significantly more efficient than a conventional electrostatic precipitator operated with a dc voltage. Observations show that the PEER agglomerates the fly ash and further that the SO 2 removal efficiency is improved by the presence of fly ash. The electrode configuration and performance results make retrofit consideration attractive

  19. MLS/Aura Level 2 Sulfur Dioxide (SO2) Mixing Ratio V004

    Data.gov (United States)

    National Aeronautics and Space Administration — ML2SO2 is the EOS Aura Microwave Limb Sounder (MLS) standard product for sulfur dioxide derived from radiances measured by the 240 GHz radiometer. The current...

  20. MLS/Aura L2 Sulfur Dioxide (SO2) Mixing Ratio V002

    Data.gov (United States)

    National Aeronautics and Space Administration — ML2SO2 is the EOS Aura Microwave Limb Sounder (MLS) standard product for sulfur dioxide derived from radiances measured by the 240 GHz radiometer. The current...

  1. Next-Generation Aura/OMI NO2 and SO2 Products

    Science.gov (United States)

    Krotkov, Nickolay; Yang, Kai; Bucsela, Eric; Lamsal, Lok; Celarier, Edward; Swartz, William; Carn, Simon; Bhartia, Pawan; Gleason, James; Pickering, Ken; hide

    2011-01-01

    The measurement of both SO2 and NO2 gases are recognized as an essential component of atmospheric composition missions. We describe current capabilities and limitations of the operational Aura/OMI NO2 and SO2 data that have been used by a large number of researchers. Analyses of the data and validation studies have brought to light a number of areas in which these products can be expanded and improved. Major improvements for new NASA standard (SP) NO2 product include more accurate tropospheric and stratospheric column amounts, along with much improved error estimates and diagnostics. Our approach uses a monthly NO2 climatology based on the NASA Global Modeling Initiative (GMI) chemistry-transport model and takes advantage of OMI data from cloudy scenes to find clean areas where the contribution from the trap NO2 column is relatively small. We then use a new filtering, interpolation and smoothing techniques for separating the stratospheric and tropospheric components of NO2, minimizing the influence of a priori information. The new algorithm greatly improves the structure of stratospheric features relative to the original SP. For the next-generation OMI SO2 product we plan to implement operationally the offline iterative spectral fitting (ISF) algorithm and re-process the OMI Level-2 SO2 dataset using a priori SO2 and aerosol profiles, clouds, and surface reflectivity appropriate for observation conditions. This will improve the ability to detect and quantify weak tropospheric SO2 loadings. The new algorithm is validated using aircraft in-situ data during field campaigns in China (2005 and 2008) and in Maryland (Frostburg, 2010 and DISCOVER-AQ in July 2011). The height of the SO2 plumes will also be estimated for high SO2 loading cases (e.g., volcanic eruptions). The same SO2 algorithm will be applied to the data from OMPS sensor to be launched on NPP satellite later this year. The next-generation NO2 and SO2 products will provide critical information (e

  2. Satellite-based constraints on tropospheric volcanic emissions of SO2 and CO2

    Science.gov (United States)

    Carn, S. A.; Schwandner, F. M.

    2012-12-01

    There is considerable motivation to improve constraints on global volcanic CO2 emissions, and their partitioning between summit plumes and diffuse flank degassing; both for volcano monitoring and to better understand the role of volcanism in the global carbon cycle. One approach to refining plume CO2 degassing budgets for persistently degassing volcanoes is to obtain more accurate constraints on SO2 emissions and SO2/CO2 ratios in volcanic gases. The current generation of space-borne, hyperspectral ultraviolet (UV) nadir mapping instruments have afforded tremendous insights into the spatial and temporal variability of global, subaerial volcanic degassing of SO2. We use ~8 years of daily SO2 measurements by the Ozone Monitoring Instrument (OMI) on NASA's Aura satellite to identify and rank the strongest volcanic SO2 sources of the past decade, and compare the results to existing emissions inventories. Major SO2 sources include Ambrym (Vanuatu), Nyiragongo (DR Congo) and several volcanoes in Indonesia and Kamchatka that are largely absent from existing inventories. Typical SO2 emission rates are estimated based on the SO2 column amounts measured in the volcanic plumes. Based on this improved satellite-derived SO2 emissions inventory and existing data on SO2/CO2 ratios, we can refine estimates of plume CO2 emissions for the most prominent volcanic gas emitters. We have also used the OMI SO2 measurements to select volcanic targets for special 'stare-mode' observations of the Japanese Greenhouse Gases Observing Satellite (GOSAT) since summer 2010, to assess the potential of GOSAT shortwave-infrared (SWIR) reflectance data for detection of volcanic CO2 emissions. GOSAT measures the column-average CO2 mixing ratio (or CO2 total column) with a spatial resolution of 10 km, and hence the signal is dominated by ambient atmospheric CO2 and any seasonal cycle thereof. Further complications for volcano monitoring are that GOSAT SWIR measurements are subject to interference by

  3. MLS/Aura Near-Real-Time L2 Sulfur Dioxide (SO2) Mixing Ratio V003

    Data.gov (United States)

    National Aeronautics and Space Administration — ML2SO2_NRT is the EOS Aura Microwave Limb Sounder (MLS) Near-Real-Time (NRT) product for sulfur dioxide (SO2). This product contains daily SO2 profiles taken from...

  4. Physiological responses of Norway spruce trees to elevated CO2 and SO2

    NARCIS (Netherlands)

    Tausz, M.; De Kok, L.J.; Stulen, I.

    Young Norway spruce (Picea abies (L.) Karst.) trees were exposed to elevated CO2 (0.8 mL L(-1)), SO2 (0.06 mu L L(-1)), and elevated CO2 and SO2 (0.8 mL L(-1) and 0.06 mu L L(-1), respectively) for three months. Exposure to elevated CO2 resulted in an increased biomass production of the needles,

  5. INVESTIGASI PENGARUH KONDISI LALU LINTAS DAN ASPEK METEOROLOGI TERHADAP KONSENTRASI PENCEMAR SO2 DI KOTA SEMARANG

    Directory of Open Access Journals (Sweden)

    Titik Istirokhatun

    2016-03-01

    Full Text Available The presence of air pollution in ambient air is closely related to the incidence of adverse reactions affecting human health. One of harmful pollutants and potentially major cause health problems is sulfur dioxide (SO2. The number of vehicles that are passing and queuing on the crossroads because of traffic light can affect the concentration of SO2. Besides, in these locations there are a lot of road users which are potentially exposed by contaminants, so information about the concentration of SO2 is important to know. This study aimed to investigate the impact of meteorological factors and the number of vehicles on SO2 concentrations. Impinger was used for air sampling, and pararosaniline method was used for determining SO2 concentration. Sampling and calculation of the number of passing vehicles were performed 3 times ie in the morning, afternoon and evening. Based on the results of the study, the highest concentrations of SO2 were on the range of 15-21 mg/Nm3. .

  6. Effects of SO2 and NO x control on energy-efficiency power generation

    International Nuclear Information System (INIS)

    Graus, W.H.J.; Worrell, E.

    2007-01-01

    The aim of this paper is to give an overview of the effects of SO 2 and NO x pollution control on the energy efficiency of fossil-fired power generation for the following countries: Australia, China, France, Germany, India, Japan, Nordic countries (Denmark, Finland, Sweden, and Norway aggregated), South Korea, UK and Ireland, and United States. Together these countries generate 65% of fossil-fired power generation worldwide. The level of SO 2 and NO x control seems to vary widely for the included countries. The highest level of desulphurisation and denitrification is present in Japan, Germany, Nordic countries and South Korea. These countries also have the lowest NO x and SO 2 emissions per unit of power generated. Limited pollution control is implemented in India and China, resulting in high specific NO x and SO 2 emissions. The effect of NO x and SO 2 control on net energy efficiency is estimated to be around 2% for coal-fired power plants and 1% for natural gas-fired power plants. The average power use for NO x and SO 2 control for fossil-fired power generation is estimated to be between 1.2% and 1.5% of power generation output for countries with high levels of pollution control; leading to an effect on net efficiency of fossil-fired power generation of 0.5-0.6% points

  7. SO2-sensing characteristics of NASICON sensors with ZnSnO3 sensing electrode

    International Nuclear Information System (INIS)

    Zhong Tiegang; Quan Baofu; Liang Xishuang; Liu Fengmin; Wang Biao

    2008-01-01

    A compact tubular sensor based on sodium super ionic conductor (NASICON) and ZnSnO 3 sensing electrode was designed for the detection of sulfur dioxide. The NASICON and ZnSnO 3 material were prepared by sol-gel method and were analyzed by the X-ray diffraction (XRD) analysis, respectively. And ZnSnO 3 materials were analyzed by SEM. ZnSnO 3 thick film was prepared to investigate characteristics of sulfur dioxide (SO 2 ) at various operating temperatures. The sensor using ZnSnO 3 gave excellent sensing properties to 5-50 ppm SO 2 in air at 360-390 deg. C. The EMF value of the sensor was almost proportional to the logarithm of SO 2 concentration, the sensitivity (slope) was 255 mV/decade at 375 deg. C. It was also seen that the sensor showed a good selectivity to SO 2 against H 2 S, NO 2 , Cl 2 , NO and C 7 H 8 . The sensor had speedy response kinetics to SO 2 too, the 90% response time to 5, 10, 20 and 50 ppm SO 2 was 18, 10, 8 and 5 s, respectively, and the recovery time was 27, 99, 184 and 243 s, respectively. Finally, a sensing mechanism involved the mixed potential was proposed

  8. Removal kinetics for gaseous NO and SO2by an aqueous NaClO2solution mist in a wet electrostatic precipitator

    KAUST Repository

    Park, Hyun-Woo

    2016-07-26

    Removal kinetics for NO and SO2 by NaClO2 solution mist were investigated in a wet electrostatic precipitator. By varying the molar concentrations of NO, SO2, and NaClO2, the removal rates of NO and SO2 confirmed to range from 34.8 to 72.9 mmol/m3 s and 36.6 to 84.7 mmol/m3 s, respectively, at a fixed gas residence time of 0.25 s. The rate coefficients of NO and SO2 were calculated to be 0.679 (mmol/m3)−0.33 s−1 and 1.401 (mmol/m3)−0.1 s−1 based on the rates of the individual removal of NO and SO2. Simultaneous removal of NO and SO2 investigated after the evaluation of removal rates for their individual treatment was performed. At a short gas residence time, SO2 gas removed more quickly by a mist of NaClO2 solution than NO gas in simultaneous removal experiments. This is because SO2 gas, which has a relatively high solubility in solution, was absorbed more rapidly at the gas–liquid interface than NO gas. NO and SO2 gases were absorbed as nitrite (Formula presented.) and sulfite (Formula presented.) ions, respectively, by the NaClO2 solution mist at the gas–liquid interface. Then, (Formula presented.) and (Formula presented.) were oxidized to nitrate (Formula presented.) and sulfate (Formula presented.), respectively, by reactions with (Formula presented.), ClO2, HClO, and ClO in the liquid phase. © 2016 Informa UK Limited, trading as Taylor & Francis Group

  9. High-Temperature Corrosion of AlCrSiN Film in Ar-1%SO2 Gas

    Directory of Open Access Journals (Sweden)

    Poonam Yadav

    2017-03-01

    Full Text Available AlCrSiN film with a composition of 29.1Al-17.1Cr-2.1Si-51.7N in at. % was deposited on a steel substrate by cathodic arc ion plating at a thickness of 1.8 μm. It consisted of nanocrystalline hcp-AlN and fcc-CrN, where a small amount of Si was dissolved. Corrosion tests were carried out at 800 °C for 5–200 h in Ar-1%SO2 gas. The major corrosion reaction was oxidation owing to the high oxygen affinity of Al and Cr in the film. The formed oxide scale consisted primarily of (Al,Cr2O3, within which Fe, Si, and S were dissolved. Even after corrosion for 200 h, the thickness of the scale was about 0.7–1.2 μm, indicating that the film had good corrosion resistance in the SO2-containing atmosphere.

  10. Applying UV cameras for SO2 detection to distant or optically thick volcanic plumes

    Science.gov (United States)

    Kern, Christoph; Werner, Cynthia; Elias, Tamar; Sutton, A. Jeff; Lübcke, Peter

    2013-01-01

    Ultraviolet (UV) camera systems represent an exciting new technology for measuring two dimensional sulfur dioxide (SO2) distributions in volcanic plumes. The high frame rate of the cameras allows the retrieval of SO2 emission rates at time scales of 1 Hz or higher, thus allowing the investigation of high-frequency signals and making integrated and comparative studies with other high-data-rate volcano monitoring techniques possible. One drawback of the technique, however, is the limited spectral information recorded by the imaging systems. Here, a framework for simulating the sensitivity of UV cameras to various SO2 distributions is introduced. Both the wavelength-dependent transmittance of the optical imaging system and the radiative transfer in the atmosphere are modeled. The framework is then applied to study the behavior of different optical setups and used to simulate the response of these instruments to volcanic plumes containing varying SO2 and aerosol abundances located at various distances from the sensor. Results show that UV radiative transfer in and around distant and/or optically thick plumes typically leads to a lower sensitivity to SO2 than expected when assuming a standard Beer–Lambert absorption model. Furthermore, camera response is often non-linear in SO2 and dependent on distance to the plume and plume aerosol optical thickness and single scatter albedo. The model results are compared with camera measurements made at Kilauea Volcano (Hawaii) and a method for integrating moderate resolution differential optical absorption spectroscopy data with UV imagery to retrieve improved SO2 column densities is discussed.

  11. Impact of Manufacturing Transfer on SO2 Emissions in Jiangsu Province, China

    Directory of Open Access Journals (Sweden)

    Ying Peng

    2016-05-01

    Full Text Available The impact of manufacturing transfer in Jiangsu province, China, on the spatial-temporal variations of SO2 emissions is investigated using estimated sector-specific SO2 emissions, and emissions in the different transfer-in and transfer-out regions were quantified during 2000–2011. Our results show that SO2 emissions had undergone three phases: an increase in the period of 2000–2005, a rapid decline in 2005–2008 and a slow decline in 2008–2011. Emissions from the south dominated the total emissions in the province. Cleaner production generally contributed to the reduced emissions, but rather, at the industrial scale. Pollution abatement was occasional and industrial structure was negligible in some years. The three phases also coincided with the three periods of the manufacturing transfer: transferred to the south from outside the province during 2000–2005, to the central from the south within the province during 2005–2008 and to the north from the south or partly from the inner central within the province during 2008–2011. With the manufacturing transfer, SO2 emission magnitudes and distributions were also changed. In the south, −12.36 and −5.62 Mt of SO2 emissions were transferred out during 2005–2008 and 2008–2011, respectively. Forty-three-point-four percent and 56.4% of the SO2 emissions in the south were transferred to the central and north during 2005–2008, respectively. The north region received 77.7% and 22.1% of SO2 emissions from the south and the central region during 2008–2011, respectively. The paper reveals that structure adjustments should be executed in a timely manner in the manufacturing transfer-in process so that the transfer-in regions can benefit from the economic boom without bearing a deteriorated environment.

  12. A new method research of monitoring low concentration NO and SO2 mixed gas

    Science.gov (United States)

    Bo, Peng; Gao, Chao; Guo, Yongcai; Chen, Fang

    2018-01-01

    In order to reduce the pollution of the environment, China has implemented a new ultra-low emission control regulations for polluting gas, requiring new coal-fired power plant emissions SO2 less than 30ppm, NO less than 75ppm, NO2 less than 50ppm, Monitoring low concentration of NO and SO2 mixed gases , DOAS technology facing new challenges, SO2 absorb significantly weaken at the original absorption peak, what more the SNR is very low, it is difficult to extract the characteristic signal, and thus cannot obtain its concentration. So it cannot separate the signal of NO from the mixed gas at the wavelength of 200 230nm through the law of spectral superposition, it cannot calculate the concentration of NO. The classical DOAS technology cannot meet the needs of monitoring. In this paper, we found another absorption spectrum segment of SO2, the SNR is 10 times higher than before, Will not be affected by NO, can calculate the concentration of SO2 accurately, A new method of segmentation and demagnetization separation technology of spectral signals is proposed, which achieves the monitoring the low concentration mixed gas accurately. This function cannot be achieved by the classical DOAS. Detection limit of this method is 0.1ppm per meter which is higher than before, The relative error below 5% when the concentration between 0 5ppm, the concentration of NO between 6 75ppm and SO2 between 6 30ppm the relative error below 1.5%, it has made a great breakthrough In the low concentration of NO and SO2 monitoring. It has great scientific significance and reference value for the development of coal-fired power plant emission control, atmospheric environmental monitoring and high-precision on-line instrumentation.

  13. Applying UV cameras for SO2 detection to distant or optically thick volcanic plumes

    Science.gov (United States)

    Kern, Christoph; Werner, Cynthia; Elias, Tamar; Sutton, A. Jeff; Lübcke, Peter

    2013-07-01

    Ultraviolet (UV) camera systems represent an exciting new technology for measuring two dimensional sulfur dioxide (SO2) distributions in volcanic plumes. The high frame rate of the cameras allows the retrieval of SO2 emission rates at time scales of 1 Hz or higher, thus allowing the investigation of high-frequency signals and making integrated and comparative studies with other high-data-rate volcano monitoring techniques possible. One drawback of the technique, however, is the limited spectral information recorded by the imaging systems. Here, a framework for simulating the sensitivity of UV cameras to various SO2 distributions is introduced. Both the wavelength-dependent transmittance of the optical imaging system and the radiative transfer in the atmosphere are modeled. The framework is then applied to study the behavior of different optical setups and used to simulate the response of these instruments to volcanic plumes containing varying SO2 and aerosol abundances located at various distances from the sensor. Results show that UV radiative transfer in and around distant and/or optically thick plumes typically leads to a lower sensitivity to SO2 than expected when assuming a standard Beer-Lambert absorption model. Furthermore, camera response is often non-linear in SO2 and dependent on distance to the plume and plume aerosol optical thickness and single scatter albedo. The model results are compared with camera measurements made at Kilauea Volcano (Hawaii) and a method for integrating moderate resolution differential optical absorption spectroscopy data with UV imagery to retrieve improved SO2 column densities is discussed.

  14. The contribution of ocean-leaving DMS to the global atmospheric burdens of DMS, MSA, SO2, and NSS SO4=

    NARCIS (Netherlands)

    van Himbergen-Gondwe, P.M.; Krol, M.; Gieskes, W.W C; Klaassen, W.; de Baar, H.J.W.

    2003-01-01

    [1] The contribution of ocean-derived DMS to the atmospheric burdens of a variety of sulphur compounds (DMS, MSA, SO2, and nss SO4=) is quantified from season to season. Such quantification, especially for nss SO4= (the climate-relevant product of DMS oxidation), is essential for the quantification

  15. Sulfur Isotope Fractionation Due to SO2 Photolysis in the Atmosphere

    Science.gov (United States)

    Lyons, J. R.; Blackie, D.; Stark, G.; Pickering, J.

    2012-12-01

    The discovery of unusual (i.e. mass-independent) sulfur isotope fractionation (or MIF) in Archean and Paleoproterozoic sedimentary rocks has promised to yield insights into the rise of O2 and the nature of the sulfur cycle on ancient Earth [1], but interpretation has been hampered by the lack of a clear mechanism for the sulfur isotope signature. Proposed MIF mechanisms include SO2 photolysis [1-4], atmospheric S3 (thiozone) formation, and thermal sulfate reduction in sediments [5]. Studies focusing only on SO2 photolysis, including measurements of isotopic cross sections [6], have yielded results differing greatly from theory [4], and have resulted in improbable interpretations [7]. In addition to ancient rocks, there are sulfur isotope MIF signatures in polar ice core sulfates associated with massive Plinian eruptions over the past ~1000 years (e.g., [8]). The ice core MIF signatures differ significantly from the ancient Earth MIF signatures, suggesting a different source mechanism. SO2 photolysis can generate sulfur isotope MIF signatures in two ways: 1) self-shielding by an optically-thick column of SO2, and 2) isotope-dependent differences in absorption line intensities and widths, which are espcially important for optically-thin conditions. The MIF signatures in ice core sulfates appear to be consistent with self-shielding in an optically-thick plume, but the Archean MIF clearly is not. To address the optically-thin case, we've made high-resolution ultraviolet cross section measurements of the sulfur isotopologues of SO2 made with the UV FTS at Imperial College. We measured cross sections at 1 cm-1 spectral resolution for 32SO2, 33SO2, 34SO2 and for a 36SO2/34SO2 mixture. Incorporating these cross sections into a simple atmospheric photochemical model with a solar UV flux, we find sulfur MIF signatures for SO and S that.are consistent with the Archean pyrites. We also find that additional mass-dependent fractionation during self-shielding by 32SO2 places an

  16. Arc-scale observations of volcanic SO2: a case study from Papua New Guinea

    Science.gov (United States)

    McCormick, B. T.; Edmonds, M.; Mather, T. A.; Carn, S. A.

    2011-12-01

    It is now possible to quantify volcanic arc-scale volcanic gas emissions using satellite-based instruments. We have used the Ozone Monitoring Instrument (OMI) to measure both the non-explosive and explosive eruption output of sulphur dioxide (SO2) from volcanoes along the Papua New Guinea arc between 2005-2008. Very few estimates of arc-scale volcanic SO2 output exist to date, primarily due to difficulties inherent in ground-based measurements and the high detection limits of previous generations of satellite-based instruments. The high spatial resolution and low detection limits of OMI mean that even low-level passive degassing can be detected, opening up new possibilities for arc-scale observations. These observations are of use for volcano monitoring, hazard assessment (particularly with regard to aviation hazard) and assessment of arc geochemical budgets and are of immense value in remote regions with little ground-based instrumentation, such as Papua New Guinea. We identify Manam, Langila, Ulawun, Rabaul and Bagana as the active sources of volcanic SO2 in Papua New Guinea, with Bagana being the single largest source. Our OMI time series shows that over the four year period, ~1.5 ± 0.5 Mt SO2 was degassed from the arc and the emissions were dominated by major eruption events at Manam (January 2005), Bagana (June 2006) and Rabaul (October 2006). Averaged over the past century however, we find that major explosive eruptions contribute Papua New Guinea's annual volcanic SO2 emissions are similar to those from previously published satellite-based studies of other volcanic arc settings. Ground-based measurements of SO2 at five of Papua New Guinea's volcanoes in 2003 are consistent with our satellite-based observations. Uncertainties in our estimate of arc SO2 output include the effect of in-plume chemical processing of SO2 prior to the satellite overpass and the limitations to OMI's visualisation of low-levels of SO2 emitted into the planetary boundary layer rather

  17. Sulphur dioxide (SO2) emissions during the 2014-15 Fogo eruption, Cape Verde

    Science.gov (United States)

    Barrancos, José; Dionis, Samara; Quevedo, Roberto; Fernandes, Paulo; Rodríguez, Fátima; Pérez, Nemesio M.; Silva, Sónia; Cardoso, Nadir; Hernández, Pedro A.; Melián, Gladys V.; Padrón, Eleazar; Padilla, Germán; Asensio-Ramos, María; Calvo, David; Semedo, Helio; Alfama, Vera

    2015-04-01

    A new eruption started at Fogo volcanic island on November 23, 2014, an active stratovolcano, located in the SW of the Cape Verde Archipelago; rising over 6 km from the 4000m deep seafloor to the Pico do Fogo summit at 2829m above sea level (m.a.s.l.). Since settlement in the 15th century, 27 eruptions have been identified through analysis of incomplete written records (Ribeiro, 1960), with average time intervals of 20 yr and average duration of two months. The eruptions were mostly effusive (Hawaiian to Strombolian), with rare occurrences of highly explosive episodes including phreatomagmatic events (Day et al., 1999). This study reports sulphur dioxide (SO2) emission rate variations observed throughout the 2014-15 Fogo eruption, Cape Verde. More than 100 measurements of SO2 emission rate have been carried out in a daily basis by ITER/INVOLCAN/UNICV/OVCV/SNPC research team since November 28, 2014, five days after the eruption onset, by means of a miniDOAS using the traverse method with a car. The daily deviation obtained of the data is around 15%. Estimated SO2 emission rates ranged from 12,476 ± 981 to 492 ± 27 tons/day during the 2014-15 Fogo eruption until January 1, 2015. During this first five days of measurements, the observed SO2 emission rates were high with an average rate of 11,100 tons/day. On December 3, 2014 the SO2 emission rate dropped to values close to 4,000 tons/day, whereas few days later, on December 10, 2014, an increase to values close to 11,000 tons/day was recorded. Since then, SO2 emission rate has shown decrease trend to values close to 1,300 tons/day until December 21, 2014. The average of the observed SO2 emission rate was about 2,000 tons/day from December 21, 2014 to January 1, 2015, without detecting a specific either increasing or decreasing trend of the SO2 emission rate. The objective of this report is to clarify relations between the SO2 emission rate and surface eruptive activity during the 2014-15 Fogo eruption. Day, S. J

  18. Preliminary performance and operating results from the integrated dry NOx/SO2 emissions control system

    International Nuclear Information System (INIS)

    Hunt, T.; Schott, G.; Smith, R.; Muzio, L.; Jones, D.; Mali E.; Arrigoni, T.

    1993-01-01

    The Integrated Dry NO x /SO 2 Emissions Control System was installed at Public Service Company of Colorado's Arapaho 4 generating station in 1992 in cooperation with the U.S. Department of Energy (DOE) and and the Electric Power Research Institute (EPRI). This full scale 100 MWe demonstration combines low-NO x burners, overfire air, and selective noncatalytic reduction (SNCR) for NO x control and dry sorbent injection with humidification for SO 2 control. Operation and testing of the Integrated Dry NO x /SO 2 Emissions Control System began in August 1992 and will continue through mid 1994. Preliminary results of the NO x control technologies show that the original system goal of 70% NO x removal has been easily met and that NO x removals of up to 80% are possible at full load with the combustion and SNCR systems. Testing of the dry sorbent injection system with low sulfur coal began in April 1993 using a calcium-based reagent. A maximum SO 2 removal of 40% has been achieved with duct injection of commercial calcium hydroxide and humidification to a 25 degrees F approach to saturation. Sodium-based dry sorbent injection is expected to achieved up to a 70% SO 2 reduction

  19. A density functional theory insight towards the rational design of ionic liquids for SO2 capture.

    Science.gov (United States)

    García, Gregorio; Atilhan, Mert; Aparicio, Santiago

    2015-05-28

    A systematic density functional theory (DFT) analysis has been carried out to obtain information at the molecular level on the key parameters related to efficient SO2 capture by ionic liquids (ILs). A set of 55 ILs, for which high gas solubility is expected, has been selected. SO2 solubility of ILs was firstly predicted based on the COSMO-RS (Conductor-like Screening Model for Real Solvents) method, which provides a good prediction of gas solubility data in ILs without prior experimental knowledge of the compounds' features. Then, interactions between SO2 and ILs were deeply analyzed through DFT simulations. This work provides valuable information about required factors at the molecular level to provide high SO2 solubility in ILs, which is crucial for further implementation of these materials in the future. In our opinion, systematic research on ILs for SO2 capture increases our knowledge about those factors which could be controlled at the molecular level, providing an approach for the rational design of task-specific ILs.

  20. Partial discharge early-warning through ultraviolet spectroscopic detection of SO2

    International Nuclear Information System (INIS)

    Zhao, Yu; Wang, Xianpei; Dai, Dangdang; Dong, Zhengcheng; Huang, Yunguang

    2014-01-01

    Surveillance of SF 6  decomposition products is significant for detection of partial discharge (PD) in gas insulation switchgear (GIS). As a basis in on-site detection and diagnosis, PD early-warning aims to quickly find the abnormalities using a simple and cheap device. In this paper, SO 2  is chosen as a feature product and detected through ultraviolet spectroscopy. The derivative method is employed for baseline correction and spectral enhancement. The standard gases of the main decomposition products are qualitatively and quantitatively detected. Then decomposition experiments with different defects are designed to further verify the feasibility. As a stable decomposition product under PD, SO 2  is proved to be applicable for PD early-warning in the field. By selecting the appropriate wavelength range, namely 290–310 nm, ultraviolet derivative spectroscopy is sensitive enough to the trace SO 2  in the decomposed gas and the interference of other products can be avoided. Fast Fourier transform could be used for feature extraction in qualitative detection. Concentrations of SO 2  and other by-products increase with increasing discharge time and could be affected by the discharge energy and PD type. Ultraviolet detection based on SO 2  is effective for PD early-warning but the threshold should still be carefully selected in practice. (paper)

  1. Temperature impact on SO2 removal efficiency by ammonia gas scrubbing

    International Nuclear Information System (INIS)

    He Boshu; Zheng Xianyu; Wen Yan; Tong Huiling; Chen Meiqian; Chen Changhe

    2003-01-01

    Emissions reduction in industrial processes, i.e. clean production, is an essential requirement for sustainable development. Fossil fuel combustion is the main emission source for gas pollutants, such as NO X , SO 2 and CO 2 , and coal is now a primary energy source used worldwide with coal combustion being the greatest atmospheric pollution source in China. This paper analyzes flue gas cleaning by ammonia scrubbing (FGCAS) for power plants to remove gaseous pollutants, such as NO X , SO 2 and CO 2 , and presents the conceptual zero emission design for power plants. The byproducts from the FGCAS process can be used in agriculture or for gas recovery. Experimental results presented for SO 2 removal from the simulated flue gas in a continuous flow experiment, which was similar to an actual flue gas system, showed that the effectiveness of the ammonia injection or scrubbing depends on the temperature. The FGCAS process can effectively remove SO 2 , but the process temperature should be below 60 deg. C or above 80 deg. C for SO 2 reduction by NH 3 scrubbing

  2. Simultaneous removal of NO and SO2using vacuum ultraviolet light (VUV)/heat/peroxymonosulfate (PMS).

    Science.gov (United States)

    Liu, Yangxian; Wang, Yan; Wang, Qian; Pan, Jianfeng; Zhang, Jun

    2018-01-01

    Simultaneous removal process of SO 2 and NO from flue gas using vacuum ultraviolet light (VUV)/heat/peroxymonosulfate (PMS) in a VUV spraying reactor was proposed. The key influencing factors, active species, reaction products and mechanism of SO 2 and NO simultaneous removal were investigated. The results show that vacuum ultraviolet light (185 nm) achieves the highest NO removal efficiency and yield of and under the same test conditions. NO removal is enhanced at higher PMS concentration, light intensity and oxygen concentration, and is inhibited at higher NO concentration, SO 2 concentration and solution pH. Solution temperature has a double impact on NO removal. CO 2 concentration has no obvious effect on NO removal. and produced from VUV-activation of PMS play a leading role in NO removal. O 3 and ·O produced from VUV-activation of O 2 also play an important role in NO removal. SO 2 achieves complete removal under all experimental conditions due to its very high solubility in water and good reactivity. The highest simultaneous removal efficiency of SO 2 and NO reaches 100% and 91.3%, respectively. Copyright © 2017 Elsevier Ltd. All rights reserved.

  3. Model calculations of competing climatic effects of SO2 and CO2 in fossil fuel combustion

    International Nuclear Information System (INIS)

    Rajeevan, M.; Sinha Ray, K.C.; Srivastava, H.N.

    1995-01-01

    Fossil fuel combustion has two competing effects on the climate system, a warming due to the emission of CO 2 and other trace gases and a cooling due to sulphate particles formed from the SO 2 emission. A detailed parameterization of the relationship between fossil fuel burning and the SO 2 effect on backscattering and cloud albedo is implemented in a one-dimensional radiative-convective model for assessing the climatic impact. The results show that at present the cooling induced by the combined effect of SO 2 completely counteracts the CO 2 greenhouse warming. The model predicts that by the year 2060 the SO 2 -induced cooling reduces warming due to CO 2 by 66% in the Intergovernmental Panel for Climate Change (IPCC) scenario Business-as-Usual (BAU) and by 27% in the IPCC scenario D. Attempts to slow-pace the fossil fuel burning will decrease the SO 2 concentration, which could further increase global warming. (author). 26 refs., 7 figs

  4. Simultaneous purifying of Hg0, SO2, and NOx from flue gas by Fe3+/H2O2: the performance and purifying mechanism.

    Science.gov (United States)

    Xing, Yi; Li, Liuliu; Lu, Pei; Cui, Jiansheng; Li, Qianli; Yan, Bojun; Jiang, Bo; Wang, Mengsi

    2018-03-01

    Hg 0 , SO 2 , and NOx result in heavily global environmental pollution and serious health hazards. Up to now, how to efficiently remove mercury with SO 2 and NOx from flue gas is still a tough task. In this study, series of high oxidizing Fenton systems were employed to purify the pollutants. The experimental results showed that Fe 3+ /H 2 O 2 was more suitable to purify Hg 0 than Fe 2+ /H 2 O 2 and Cu 2+ /H 2 O 2. The optimal condition includes Fe 3+ concentration of 0.008 mol/L, Hg 0 inlet concentration of 40 μg/m 3 , solution temperature of 50 °C, pH of 3, H 2 O 2 concentration of 0.7 mol/L, and O 2 percentage of 6%. When SO 2 and NOx were taken into account under the optimal condition, Hg 0 removal efficiency could be enhanced to 91.11% while the removal efficiency of both NOx and SO 2 was slightly declined, which was consistent to the analysis of purifying mechanism. The removal efficiency of Hg 0 was stimulated by accelerating the conversion of Fe 2+ to Fe 3+ , which resulted from the existence of SO 2 and NOx. The results of this study suggested that simultaneously purifying Hg 0 , SO 2 , and NOx from flue gas is feasible.

  5. SO2 gas adsorption by modified kaolin clays: influence of previous heating and time acid treatments.

    Science.gov (United States)

    Volzone, Cristina; Ortiga, Jose

    2011-10-01

    Modified kaolin clays were used as adsorbents for SO(2) gas adsorptions. The clays were heated up to 900 °C previous to acid treatments with 0.5 N sulfuric acid solutions at boiling temperature during different times up to 1440 min. Equilibrium adsorption at 25 °C and 0.1 MPa was carried out by using a volumetric apparatus. The samples were characterized by chemical analysis, X-ray diffraction and infrared analysis. The heating of the clays followed by acid treatment improved the adsorption capacity of the kaolin clays. The presence of amorphous silica and hydroxyl in the final products improved SO(2) adsorption capacity. Better properties for SO(2) adsorption were found in kaolin rich in not well ordered kaolinite clay mineral. Copyright © 2011 Elsevier Ltd. All rights reserved.

  6. Comparison of SO2 and NO2 observations from OMI and OMPS from 2012 to 2016

    Science.gov (United States)

    Wang, Y.; Wang, J.; Xu, X.; Yang, K.

    2017-12-01

    Both Sulfur dioxide (SO2) and nitrogen dioxide (NO2) are precursors of PM2.5 which has significant impacts on human health. We compare observations from Ozone Monitoring Instrument (OMI) which has data gap due to row anomaly and Ozone Mapping Profiler Suite (OMPS) that is currently the only operational UV satellite sensor providing contiguous daily global coverage. In this study, we examine changes of SO2 and NO2 in several polluted regions and see both upward trends and downward trends in different areas but trends observed by the two sensors are consistent in general. Some of these upward and downward trends are associated with economic development and implementation of emission control policy. In addition, we analyzed probability distribution function of SO2 and NO2 from the two sensors and how row anomaly effect the intercomparison.

  7. Dissociative phototionization cross sections of H2, SO2 and H2O

    International Nuclear Information System (INIS)

    Chung, Y.

    1989-01-01

    The partial photoionization cross sections of H 2 , SO 2 , and H 2 O were calculated from the measured photoionization branching ratios and the known total photoionization cross sections. The branching ratios were measured with a time-of-flight mass spectrometer and synchrotron radiation. The branching ratios Of H 2 , SO 2 , and H 2 O were measured for 100 ∼ 410, 150 ∼ 380 and 120 ∼ 720 angstrom. The author also measured the photoionization yield Of SO 2 from 520 to 665 angstrom using a double ion chamber and a glow discharge light source. The principle of a time-of-flight mass spectrometer is explained. New calculations were made to see how the design of the mass spectrometer, applied voltage, and kinetic energy of the ions affect the overall performance of the mass spectrometer. Several useful techniques that we used at the synchrotron for wavelength calibration and higher order suppression are also discussed

  8. Sensitivity of Aerosol Distribution and Climate Response to Stratospheric SO2 Injection Locations

    Science.gov (United States)

    Tilmes, Simone; Richter, Jadwiga H.; Mills, Michael J.; Kravitz, Ben; MacMartin, Douglas G.; Vitt, Francis; Tribbia, Joseph J.; Lamarque, Jean-Francois

    2017-12-01

    Injection of SO2 into the stratosphere has been proposed as a method to, in part, counteract anthropogenic climate change. So far, most studies investigated injections at the equator or in a region in the tropics. Here we use Community Earth System Model version 1 Whole Atmosphere Community Climate Model (CESM1(WACCM)) to explore the impact of continuous single grid point SO2 injections at seven different latitudes and two altitudes in the stratosphere on aerosol distribution and climate. For each of the 14 locations, 3 different constant SO2 emission rates were tested to identify linearity in aerosol burden, aerosol optical depth, and climate effects. We found that injections at 15°N and 15°S and at 25 km altitude have equal or greater effect on radiation and surface temperature than injections at the equator. Nonequatorial injections transport SO2 and sulfate aerosols more efficiently into middle and high latitudes and result in particles of smaller effective radius and larger aerosol burden in middle and high latitudes. Injections at 15°S produce the largest increase in global average aerosol optical depth and increase the change in radiative forcing per Tg SO2/yr by about 15% compared to equatorial injections. High-altitude injections at 15°N produce the largest reduction in global average temperature of 0.2° per Tg S/yr for the last 7 years of a 10 year experiment. Injections at higher altitude are generally more efficient at reducing surface temperature, with the exception of large equatorial injections of at least 12 Tg SO2/yr. These findings have important implications for designing a strategy to counteract global climate change.

  9. Aura OMI observations of regional SO2 and NO2 pollution changes from 2005 to 2015

    Science.gov (United States)

    Krotkov, Nickolay A.; McLinden, Chris A; Li, Can; Lamsal, Lok N.; Celarier, Edward A.; Marchenko, Sergey V.; Swartz, William H.; Bucsela, Eric J.; Joiner, Joanna; Duncan, Bryan N.; hide

    2016-01-01

    The Ozone Monitoring Instrument (OMI) onboard NASA's Aura satellite has been providing global observations of the ozone layer and key atmospheric pollutant gases, such as nitrogen dioxide (NO2/ and sulfur dioxide (SO2/, since October 2004. The data products from the same instrument provide consistent spatial and temporal coverage and permit the study of anthropogenic and natural emissions on local-to-global scales. In this paper, we examine changes in SO2 and NO2 over some of the world's most polluted industrialized regions during the first decade of OMI observations. In terms of regional pollution changes, we see both upward and downward trends, sometimes in opposite directions for NO2 and SO2, for different study areas. The trends are, for the most part, associated with economic and/or technological changes in energy use, as well as regional regulatory policies. Over the eastern US, both NO2 and SO2 levels decreased dramatically from 2005 to 2015, by more than 40 and 80 %, respectively, as a result of both technological improvements and stricter regulations of emissions. OMI confirmed large reductions in SO2 over eastern Europe's largest coal-fired power plants after installation of flue gas desulfurization devices. The North China Plain has the world's most severe SO2 pollution, but a decreasing trend has been observed since 2011, with about a 50% reduction in 2012- 2015, due to an economic slowdown and government efforts to restrain emissions from the power and industrial sectors. In contrast, India's SO2 and NO2 levels from coal power plants and smelters are growing at a fast pace, increasing by more than 100 and 50 %, respectively, from 2005 to 2015. Several SO2 hot spots observed over the Persian Gulf are probably related to oil and gas operations and indicate a possible underestimation of emissions from these sources in bottom-up emission inventories. Overall, OMI observations have proved valuable in documenting rapid changes in air quality over different

  10. Experimental Study of SO2 Removal by Pulsed DBD Along with the Application of Magnetic Field

    International Nuclear Information System (INIS)

    Rong Mingzhe; Liu Dingxin; Wang Xiaohua; Wang Junhua

    2007-01-01

    Dielectric barrier discharge (DBD) for SO 2 removal from indoor air is investigated. In order to improve the removal efficiency, two novel methods are combined in this paper, namely by applying a pulsed driving voltage with nanosecond rising time and applying a magnetic field. For SO 2 removal efficiency, different matches of electric field and magnetic field are discussed. And nanosecond rising edge pulsed power supply and microsecond rising edge pulsed power supply are compared. It can be concluded that a pulsed DBD with nanosecond rising edge should be adopted, and electrical field and magnetic field should be applied in an appropriate match

  11. Aura OMI observations of regional SO2 and NO2 pollution changes from 2005 to 2015

    Directory of Open Access Journals (Sweden)

    N. A. Krotkov

    2016-04-01

    Full Text Available The Ozone Monitoring Instrument (OMI onboard NASA's Aura satellite has been providing global observations of the ozone layer and key atmospheric pollutant gases, such as nitrogen dioxide (NO2 and sulfur dioxide (SO2, since October 2004. The data products from the same instrument provide consistent spatial and temporal coverage and permit the study of anthropogenic and natural emissions on local-to-global scales. In this paper, we examine changes in SO2 and NO2 over some of the world's most polluted industrialized regions during the first decade of OMI observations. In terms of regional pollution changes, we see both upward and downward trends, sometimes in opposite directions for NO2 and SO2, for different study areas. The trends are, for the most part, associated with economic and/or technological changes in energy use, as well as regional regulatory policies. Over the eastern US, both NO2 and SO2 levels decreased dramatically from 2005 to 2015, by more than 40 and 80 %, respectively, as a result of both technological improvements and stricter regulations of emissions. OMI confirmed large reductions in SO2 over eastern Europe's largest coal-fired power plants after installation of flue gas desulfurization devices. The North China Plain has the world's most severe SO2 pollution, but a decreasing trend has been observed since 2011, with about a 50 % reduction in 2012–2015, due to an economic slowdown and government efforts to restrain emissions from the power and industrial sectors. In contrast, India's SO2 and NO2 levels from coal power plants and smelters are growing at a fast pace, increasing by more than 100 and 50 %, respectively, from 2005 to 2015. Several SO2 hot spots observed over the Persian Gulf are probably related to oil and gas operations and indicate a possible underestimation of emissions from these sources in bottom-up emission inventories. Overall, OMI observations have proved valuable in documenting rapid changes in air

  12. Updated SO2 emission estimates over China using OMI/Aura observations

    Science.gov (United States)

    Elissavet Koukouli, Maria; Theys, Nicolas; Ding, Jieying; Zyrichidou, Irene; Mijling, Bas; Balis, Dimitrios; van der A, Ronald Johannes

    2018-03-01

    The main aim of this paper is to update existing sulfur dioxide (SO2) emission inventories over China using modern inversion techniques, state-of-the-art chemistry transport modelling (CTM) and satellite observations of SO2. Within the framework of the EU Seventh Framework Programme (FP7) MarcoPolo (Monitoring and Assessment of Regional air quality in China using space Observations) project, a new SO2 emission inventory over China was calculated using the CHIMERE v2013b CTM simulations, 10 years of Ozone Monitoring Instrument (OMI)/Aura total SO2 columns and the pre-existing Multi-resolution Emission Inventory for China (MEIC v1.2). It is shown that including satellite observations in the calculations increases the current bottom-up MEIC inventory emissions for the entire domain studied (15-55° N, 102-132° E) from 26.30 to 32.60 Tg annum-1, with positive updates which are stronger in winter ( ˜ 36 % increase). New source areas were identified in the southwest (25-35° N, 100-110° E) as well as in the northeast (40-50° N, 120-130° E) of the domain studied as high SO2 levels were observed by OMI, resulting in increased emissions in the a posteriori inventory that do not appear in the original MEIC v1.2 dataset. Comparisons with the independent Emissions Database for Global Atmospheric Research, EDGAR v4.3.1, show a satisfying agreement since the EDGAR 2010 bottom-up database provides 33.30 Tg annum-1 of SO2 emissions. When studying the entire OMI/Aura time period (2005 to 2015), it was shown that the SO2 emissions remain nearly constant before the year 2010, with a drift of -0.51 ± 0.38 Tg annum-1, and show a statistically significant decline after the year 2010 of -1.64 ± 0.37 Tg annum-1 for the entire domain. Similar findings were obtained when focusing on the greater Beijing area (30-40° N, 110-120° E) with pre-2010 drifts of -0.17 ± 0.14 and post-2010 drifts of -0.47 ± 0.12 Tg annum-1. The new SO2 emission inventory is publicly available and forms

  13. Construction of Functionalized Annulated Sulfone via SO2/I Exchange of Cyclic Diaryliodonium Salts.

    Science.gov (United States)

    Wang, Ming; Chen, Shihao; Jiang, Xuefeng

    2017-09-15

    A straightforward protocol for diarylannulated sulfone construction is efficiently established via SO 2 /I exchange of iodonium(III) salts. Readily available inorganic Na 2 S 2 O 5 was served as a safe and convenient SO 2 surrogate. Diverse functionalized diarylannulated sulfones were smoothly achieved in good to excellent yields with great functional group compatibility. Organic light emitting diodes (OLEDs) material molecules were subsequently established via this method in gram scale. The unsymmetrical conjugated systems with donor-acceptor groups and π-conjugation bridges motifs, which substantially communicate electron mobility in semiconductor material molecules, were successfully afforded under the facile conditions of the exchange strategy.

  14. Model Simulations of the Competing Climatic Effects of SO2 and CO2.

    Science.gov (United States)

    Kaufman, Yoram J.; Chou, Ming-Dah

    1993-07-01

    Sulfur dioxide-derived cloud condensation nuclei are expected to enhance the planetary albedo, thereby cooling the planet. This effect might counteract the global warming expected from enhanced greenhouse gases. A detailed treatment of the relationship between fossil fuel burning and the SO2 effect on cloud albedo is implemented in a two-dimensional model for assessing the climate impact. Although there are large gaps in our knowledge of the atmospheric sources and sinks of sulfate aerosol, it is possible to reach some general conclusions. Using a conservative approach, results show that the cooling induced by the SO2 emission can presently counteract 50% of the CO2 greenhouse warming. Since 1980, a strong warming trend has been predicted by the model, 0.15°C, during the 1980-1990 period alone. The model predicts that by the year 2060 the SO2 cooling reduces climate warming by 0.5°C or 25% for the Intergovernmental Panel on Climate Change (IPCC) business as usual (BAU) scenario and 0.2°C or 20% for scenario D (for a slow pace of fossil fuel burning). The hypothesis is examined that the different responses between the Northern Hemisphere (NH) and the Southern Hemisphere (SH) can be used to validate the presence of the SO2-induced cooling. Despite the fact that most of the SO2-induced cooling takes place in the Northern Hemispheric continents, the model-predicted difference in the temperature response between the NH and the SH of 0.2°C in 1980 is expected to remain about the same at least until 2060. This result is a combined effect of the much faster response of the continents than the oceans and of the larger forcing due to CO2 than due to the SO2. The climatic response to a complete filtering of SO2 from the emission products in order to reduce acid rain is also examined. The result is a warming surge of 0.4°C in the first few years after the elimination of the SO2 emission.

  15. Retrieval columns of SO2 in industrial chimneys using DOAS passive in traverse

    Science.gov (United States)

    Galicia Mejía, Rubén; de la Rosa Vázquez, José Manuel; Sosa Iglesias, Gustavo

    2011-10-01

    The optical Differential Optical Absorption Spectroscopy (DOAS) is a technique to measure pollutant emissions like SO2, from point sources and total fluxes in the atmosphere. Passive DOAS systems use sunlight like source. Measurements with such systems can be made in situ and in real time. The goal of this work is to report the implementation of hardware and software of a portable system to evaluate the pollutants emitted in the atmosphere by industrial chimneys. We show SO2 measurements obtained around PEMEX refinerys in Tula Hidalgo that enables the identification of their pollution degree with the knowledge of speed wind.

  16. Aura OMI Observations of Global SO2 and NO2 Pollution from 2005 to 2013

    Science.gov (United States)

    Krotkov, Nickolay; Li, Can; Lamsal, Lok; Celarier, Edward; Marchenko, Sergey; Swartz, William H.; Bucsela, Eric; Fioletov, Vitali; McLinden, Chris; Joiner, Joanna; hide

    2014-01-01

    The Ozone Monitoring Instrument (OMI), a NASA partnership with the Netherlands and Finland, flies on the NASA Aura satellite and uses reflected sunlight to measure the two critical atmospheric trace gases: nitrogen dioxide (NO2) and sulfur dioxide (SO2) characterizing daily air quality. Both gases and the secondary pollutants they produce (particulate matter, PM2.5, and tropospheric ozone) are USEPA designated criteria pollutants, posing serious threats to human health and the environment (e.g., acid rain, plant damage and reduced visibility). Our group at NASA GSFC has developed and maintained OMI standard SO2 and NO2 data products. We have recently released an updated version of the standard NO2 L2 and L3 products (SP v2.1) and continue improving the algorithm. We are currently in the process of releasing next generation pollution SO2 product, based on an innovative Principal Component Analysis (PCA) algorithm, which greatly reduces the noise and biases. These new standard products provide valuable datasets for studying anthropogenic pollution on local to global scales. Here we highlight some of the OMI observed changes in air quality over several regions. Over the US average NO2 and SO2 pollution levels had decreased dramatically as a result of both technological improvements (e.g., catalytic converters on cars) and stricter regulations of emissions. We see continued decline in pollution over Europe. Over China OMI observed an increase of about 60 percent in NO2 pollution between 2005 and 2013, despite a temporal reversal of the growing trend due to both 2008 Olympic Games and the economic recession in 2009. Chinese SO2 pollution seems to have stabilized since peaking in 2007, probably due to government efforts to curb SO2 emissions from the power sector. We have also observed large increases in both SO2 and NO2 pollution particularly in Eastern India where a number of large new coal power plants had been built in recent years. We expect that further

  17. Soot and SO2 contribution to the supersites in the MILAGRO campaign from elevated flares in the Tula Refinery

    Science.gov (United States)

    Almanza, V. H.; Molina, L. T.; Sosa, G.

    2012-11-01

    This work presents a simulation of the plume trajectory emitted by flaring activities of the Miguel Hidalgo Refinery in Mexico. The flame of a representative sour gas flare is modeled with a CFD combustion code in order to estimate emission rates of combustion by-products of interest for air quality: acetylene, ethylene, nitrogen oxides, carbon monoxide, soot and sulfur dioxide. The emission rates of NO2 and SO2 were compared with measurements obtained at Tula as part of MILAGRO field campaign. The rates of soot, VOCs and CO emissions were compared with estimates obtained by Instituto Mexicano del Petróleo (IMP). The emission rates of these species were further included in WRF-Chem model to simulate the chemical transport of the plume from 22 to 27 March of 2006. The model presents reliable performance of the resolved meteorology, with respect to the Mean Absolute Error (MAE), Root Mean Square Error (RMSE), mean bias (BIAS), vector RMSE and Index of Agreement (IOA). WRF-Chem outputs of SO2 and soot were compared with surface measurements obtained at the three supersites of MILAGRO campaign. The results suggest a contribution of Tula flaring activities to the total SO2 levels of 18% to 27% at the urban supersite (T0), and of 10% to 18% at the suburban supersite (T1). For soot, the model predicts low contribution at the three supersites, with less than 0.1% at three supersites. According to the model, the greatest contribution of both pollutants to the three supersites occurred on 23 March, which coincides with the third cold surge event reported during the campaign.

  18. Absorption and desorption of SO2 in aqueous solutions of diamine-based molten salts.

    Science.gov (United States)

    Lim, Seung Rok; Hwang, Junhyeok; Kim, Chang Soo; Park, Ho Seok; Cheong, Minserk; Kim, Hoon Sik; Lee, Hyunjoo

    2015-05-30

    SO2 absorption and desorption behaviors were investigated in aqueous solutions of diamine-derived molten salts with a tertiary amine group on the cation and a chloride anion, including butyl-(2-dimethylaminoethyl)-dimethylammonium chloride ([BTMEDA]Cl, pKb=8.2), 1-butyl-1,4-dimethylpiperazinium chloride ([BDMP]Cl, pKb=9.8), and 1-butyl-4-aza-1-azoniabicyclo[2,2,2]octane chloride ([BDABCO]Cl, pKb=11.1). The SO2 absorption and desorption performance of the molten salt were greatly affected by the basicity of the molten salt. Spectroscopic, X-ray crystallographic, and computational results for the interactions of SO2 with molten salts suggest that two types of SO2-containg species could be generated depending on the basicity of the unquaternized amino group: a dicationic species comprising two different anions, HSO3(-) and Cl(-), and a monocationic species bearing Cl(-) interacting with neutral H2SO3. Copyright © 2015 Elsevier B.V. All rights reserved.

  19. What is Eating Ozone? Thermal Reactions between SO2 And O3: Implications for Icy Environments

    Science.gov (United States)

    Loeffler, Mark J.; Hudson, Reggie L.

    2016-01-01

    Laboratory studies are presented, showing for the first time that thermally driven reactions in solid H2O+SO2+O3 mixtures can occur below 150 K, with the main sulfur-containing product being bisulfate (HSO4(-)). Using a technique not previously applied to the low-temperature kinetics of either interstellar or solar system ice analogs, we estimate an activation energy of 32 kJ per mol for HSO4(-) formation. These results show that at the temperatures of the Jovian satellites, SO2 and O3 will efficiently react making detection of these molecules in the same vicinity unlikely. Our results also explain why O3 has not been detected on Callisto and why the SO2 concentration on Callisto appears to be highest on that world's leading hemisphere. Furthermore, our results predict that the SO2 concentration on Ganymede will be lowest in the trailing hemisphere, where the concentration of O3 is the highest. Our work suggests that thermal reactions in ices play a much more important role in surface and sub-surface chemistry than generally appreciated, possibly explaining the low abundance of sulfur-containing molecules and the lack of ozone observed in comets and interstellar ices.

  20. Evaluation of the Mycobacterium tuberculosis SO2 vaccine using a natural tuberculosis infection model in goats.

    Science.gov (United States)

    Bezos, J; Casal, C; Álvarez, J; Roy, A; Romero, B; Rodríguez-Bertos, A; Bárcena, C; Díez, A; Juste, R; Gortázar, C; Puentes, E; Aguiló, N; Martín, C; de Juan, L; Domínguez, L

    2017-05-01

    The development of new vaccines against animal tuberculosis (TB) is a priority for improving the control and eradication of this disease, particularly in those species not subjected to compulsory eradication programmes. In this study, the protection conferred by the Mycobacterium tuberculosis SO 2 experimental vaccine was evaluated using a natural infection model in goats. Twenty-six goats were distributed in three groups: (1) 10 goats served as a control group; (2) six goats were subcutaneously vaccinated with BCG; and (3) 10 goats were subcutaneously vaccinated with SO 2 . Four months after vaccination, all groups were merged with goats infected with Mycobacterium bovis or Mycobacterium caprae, and tested over a 40 week period using a tuberculin intradermal test and an interferon-γ assay for mycobacterial reactivity. The severity of lesions was determined at post-mortem examination and the bacterial load in tissues were evaluated by culture. The two vaccinated groups had significantly lower lesion and bacterial culture scores than the control group (P<0.05); at the end of the study, the SO 2 vaccinated goats had the lowest lesion and culture scores. These results suggest that the SO 2 vaccine provides some protection against TB infection acquired from natural exposure. Copyright © 2017 Elsevier Ltd. All rights reserved.

  1. Aura OMI observations of regional SO2 and NO2 pollution changes from 2005 to 2015

    NARCIS (Netherlands)

    Krotkov, Nickolay A.; McLinden, Chris A.; Li, Can; Lamsal, Lok N.; Celarier, Edward A.; Marchenko, Sergey V.; Swartz, William H.; Bucsela, Eric J.; Joiner, Joanna; Duncan, Bryan N.; Boersma, Folkert; Veefkind, J.P.; Levelt, Pieternel F.; Fioletov, Vitali E.; Dickerson, Russell R.; He, Hao; Lu, Zifeng; Streets, David G.

    2016-01-01

    The Ozone Monitoring Instrument (OMI) onboard NASA's Aura satellite has been providing global observations of the ozone layer and key atmospheric pollutant gases, such as nitrogen dioxide (NO2) and sulfur dioxide (SO2), since October 2004. The data products from the same instrument provide

  2. 40 CFR 60.43 - Standard for sulfur dioxide (SO2).

    Science.gov (United States)

    2010-07-01

    ...-Fired Steam Generators for Which Construction Is Commenced After August 17, 1971 § 60.43 Standard for... determined by proration using the following formula: ER13JN07.000 Where: PSSO 2 = Prorated standard for SO2... defined in appendix G of this part) at the Newton Power Station owned or operated by the Central Illinois...

  3. Absorption of 35SO2 and sulphur translocation in bean (Phaseolus vulgaris L.)

    International Nuclear Information System (INIS)

    Markowski, A.; Marcinska, I.; Pienkowski, S.; Schramel, M.; Polska Akademia Nauk, Krakow. Inst. Fizjologii Roslin)

    1977-01-01

    Absorption of 35 SO 2 by leaves of bean plants was found to depend both on the age of plants and the age of particular leaves. Differences in the ability of particular leaves to absorb sulphur were much greater in older than in younger plants. Sulphur translocation from source to sink leaves was mainly towards leaves higher up on the stem and side shoots and also to roots. Ungassed, rapidly developing leaves of side shoots had higher levels of radioactive sulphur than ungassed leaves of the main stem. Translocation to roots was greater when the lower leaves on the plant were the source. A week after gassing with 35 SO 2 a drop of radioactivity occurred in both source and sink leaves; the drop was greater in experiments with gassing individual leaves than whole plants. A week after the last exposure of leaves to 35 SO 2 labelled sulphur was found also in pods and its content increased the more the higher up on the plants were the source leaves. Sulphur dioxide absorption by leaves also depended on the degree of tissue hydration; under optimum soil moisture conditions 35 SO 2 absorption by leaves was greater than under soil drought conditions. (author)

  4. Analysis on concentration variety characteristics of SO2/NO2 in Chengdu city, southwest China

    Science.gov (United States)

    Wang, C.; Xiao, T.; Luo, Q.; WU, L.

    2017-12-01

    SO2 and NO2, the important gaseous precursors of atmospheric fine particles, are closely related to urban air quality. Chengdu located in the western China, is the capital city of Sichuan province. Though Sichuan province is one of four heavily polluted areas in China, the air pollution research in Chengdu is in a relative lack, when compared to developed cities as Beijing, Guangzhou, etc. This paper, based on characteristics of SO2 and NO2 in Chengdu, shows that: the average concentration of SO2, NO2 was 25.29 (mainly in the rage 10-40 ), 64.41 (mainly in the range 30-80 ), respectively. There is a similar annual and seasonal variation for them, yet significant differences in diurnal variation. Except summer, the air condition in Chengdu is seriously affected by SO2 and NO2, while the latter plays a more significant role. Multiple regression has good fitting performance to the diurnal variation in Chengdu. The purification efficiency of precipitation in different magnitude is also discussed. Key words: Chengdu; Pollution gas; Variety characteristics Acknowledgements: This study was supported by Pollution program in Wenjiang District, National Natural Science Foundation of China Fund Project (91337215,41575066), National Science and Technology Support Program(2015BAC03B05),Special Fund for Meteorological Re-search in the Public Interest (GYHY201406015),National Key Basic Research Program (2013CB733206), and Risk Assessment System of Significant Climate Events in Tibet (14H046), Scientific Research Foundation of CUIT (CRF201606)

  5. ACTIVATION AND REACTIVITY OF NOVEL CALCIUM-BASED SORBENTS FOR DRY SO2 CONTROL IN BOILERS

    Science.gov (United States)

    Chemically modified calcium hydroxide (Ca(OH)2) sorbents developed in the U.S. Environmental Protection Agency's Air and Energy Engineering Research Laboratory (AEERL) for sulfur dioxide (SO2) control in utility boilers were tested in an electrically heated, bench-scale isotherma...

  6. Emissioner af SO2 og NOX fra kraftværker

    DEFF Research Database (Denmark)

    Illerup, J. B.; Bruun, H. G.

    Rapporten indeholder beregninger af SO2- og NOx- emissioner fra kraftværker, der er reguleret af kvoteloven. Emissionerne er for tre forskellige produktionsscenarier beregnet ud fra emissionsfaktorer baseret på EU-direktivet om store forbrændingsanlæg og emissionsfaktorer beregnet ud fra en...

  7. Ultrastructural study of the effect of air pollution by SO2 on the ...

    African Journals Online (AJOL)

    kemrilib

    large glass bulb with a magnetic stirrer, and compressed air flow (Fig. 1). The dust ascended through an 80 cm tall vertical elutriator to eliminate the larger particles and entered the chamber from the top. SO2 entered through an injector in the center of the conical top. Chamber gas was removed through the perforated floor.

  8. First results from the permanent SO2 Camera system at Stromboli

    Science.gov (United States)

    Salerno, Giuseppe G.; Burton, Mike; Caltabiano, Tommaso; D'Auria, Luca; Maugeri, Roberto; Mure, Filippo

    2015-04-01

    Since the 1980's volcano monitoring has undergone stunning changes, evolving from descriptive and sparse observations to a systematic-quantitative approach of science and technology. Surveillance of chemical gas composition and their emission rate is a vital part of efforts in interpreting volcanic activity of observatories since their changes are closely linked with seismicity and deformation swings. In this unruly technology progression, volcanic gas sensing observations have also undergone a profound revolution, for example by increasing observation frequency of SO2 flux from a few samples per day to Hz. In May 2013, a permanent-robotic SO2 dual-camera system was installed by the Istituto Nazionale di Geofisica e Vulcanologia at Stromboli as a part of the ultraviolet scanning spectrometers network FLAME, with the intent to underpin the geochemical surveillance and shed light on degassing and volcanic processes. Here, we present the first results of SO2 flux observed by the permanent SO2 camera system in the period between May 2013 and April 2015. Results are corroborated with the well established FLAME ultraviolet scanning network and also compared with VLP signals from the seismic network.

  9. Vulcamera: a program for measuring volcanic SO2 using UV cameras

    Directory of Open Access Journals (Sweden)

    Alessandro Aiuppa

    2011-06-01

    Full Text Available We report here on Vulcamera, a stand-alone program for the determination of volcanic SO2  fluxes using ultraviolet cameras. The code enables field image acquisition and all the required post-processing operations.

  10. Ultrastructural study of the effect of air pollution by SO2 on the ...

    African Journals Online (AJOL)

    changes in airways has been suggested by smog incidents, but has not been evaluated by experiments. So, this study was done to answer the following questions: (1) What morphologic changes are produced by repeated injury to airway epithelial cells by SO2? (2) What is the time course of these morphologic features?

  11. Projection of SO2, NOx, NMVOC, particulate matter and black carbon emissions - 2015-2030

    DEFF Research Database (Denmark)

    Nielsen, Ole-Kenneth; Plejdrup, Marlene Schmidt; Hjelgaard, Katja Hossy

    This report contains a description of models and background data for projection of SO2, NOX, NMVOC, PM2.5 and black carbon for Denmark. The emissions are projected to 2030 using basic scenarios together with the expected results of a few individual policy measures. Official Danish forecasts...

  12. SO2 Emission from Active Volcanoes Measured Simultaneously by COSPEC and mini-DOAS

    Science.gov (United States)

    Barrancos, José; Roselló, José I.; Calvo, David; Padrón, Eleazar; Melián, Gladys; Hernández, Pedro A.; Pérez, Nemesio M.; Millán, Millán M.; Galle, Bo

    2008-01-01

    We measured SO2 emission rate from six volcanoes in Latin America (Santa Ana, El Salvador; San Cristóbal and Masaya, Nicaragua; Arenal and Poás, Costa Rica; Tungurahua and Sierra Negra, Ecuador) and from Mt. Etna, Italy, using two different remote sensing techniques: COSPEC (COrrelation SPECtrometer) and miniDOAS (miniaturized Differential Optical Absorption Spectroscopy). One of the goals of this study was to evaluate the differences in SO2 emission rates obtained by these two methods. The observed average SO2 emission rates measured during this study were 2688 t· d -1 from Tungurahua in July 2006, 2375 t· d -1 in September 2005 and 480 t· d -1 in February 2006 from Santa Ana, 1200 t· d -1 in May 2005 from Etna, 955 t· d -1 in March 2006 and 1165 t· d -1 in December 2006 from Masaya, 5400 t· d -1 of March 7, 2006 and 265 t· d -1 in March 2006 from San Cristobal, 113 t· d -1 in April 2006 from Arenal, 104 t· d -1 in April 2006 from Poás and 11 t· d -1 in July 2006 from Sierra Negra volcano. Most of the observed relative differences of SO2 emission measurements from COSPEC and miniDOAS were lower than 10%.

  13. SO2 and NO2 over major urban regions of India: a tempo-spatial perspective

    Science.gov (United States)

    Mallik, C.; Lal, S.

    2012-12-01

    Demographic projections show that by the year 2025, 16 of the world's 29 megacities will be located in Asia, many of which have very basic problems in terms of air quality. Apart from being home to a burgeoning population, these regions of the globe are also major players in atmospheric chemistry as a result of myriad emission patterns combined with intense photochemistry. Like most of these Asian megacities, fast-paced development in some of the Indian cities has ramifications in increased emissions from industrial and transport sectors. These emissions release sulfur dioxide (SO2) and nitrogen dioxide (NO2), in addition to several pollutants, into the ambient air and have the potential to impact the chemistry and radiative balance on a regional scale. Surface measurements of these two criteria pollutants by the Central Pollution Control Board (CPCB), India during 2005-2010 from 13 urban locations in India have been analyzed to get an insight into their temporal and spatial variability. Stations are chosen to represent the entire Indian region: Indo-Gangetic plain or 'IGP' (Jalandhar, Delhi, Kanpur, Durgapur, Kolkata, Guwahati), western India (Jodhpur, Ahmedabad, Surat), central India (Nagpur, Hyderabad) and southern India (Chennai, Trivandrum). The monthly averaged surface level SO2 and NO2 have also been compared with monthly columnar averages of these gases as detected by the Ozone monitoring Instrument (OMI) over these station grids. Mean SO2 concentrations are found to be the highest for Surat (7.5 ppbv), located in a highly industrialized region. Elevated levels of NO2, observed for Durgapur and Kolkata (31 ppbv each), are close to the 24-hour 'National Ambient Air Quality' standard (30 ppbv). The surface concentrations for both SO2 and NO2 concentrations are found to be the highest during winter. Columnar SO2 over many stations show a maximum during summer monsoon. For most IGP stations, columnar NO2 values are elevated during winter. Wavelet analyses

  14. CO2, SO2, and H2S Degassing Related to the 2009 Redoubt Eruption, Alaska

    Science.gov (United States)

    Werner, C. A.; Kelly, P. J.; Evans, W.; Doukas, M. P.; McGimsey, R. G.; Neal, C. A.

    2012-12-01

    The 2009 eruption of Redoubt Volcano, Alaska was particularly well monitored for volcanic gas emissions with 35 airborne measurements of CO2, SO2, and H2S that span from October 2008 to August 2010. Increases in CO2 degassing were detected up to 5 months prior to the eruption and varied between 3630 and 9020 tonnes per day (t/d) in the 6 weeks prior to the eruption. Increased pre-eruptive CO2 degassing was accompanied by comparatively low S emission, resulting in molar C/S ratios that ranged between 30-60. However, the C/S ratio dropped to 2.4 coincident with the first phreatic explosion on March 15, 2009, and remained steady during the explosive (March 22 - April 4, 2009), effusive dome-building (April 5 - July 1, 2009), and waning phases (August 2009 onward) of the eruption. Observations of ice-melt rates, melt water discharge, and water chemistry in the months leading up to the eruption suggested that surface waters represented drainage from surficial, perched reservoirs of condensed magmatic steam and glacial meltwater. While the surface waters were capable of scrubbing many thousands of t/d of SO2, sampling of these fluids revealed that only a few hundred tonnes of SO2 was reacting to a dissolved component each day. This is also much less than the ~ 2100 t/d SO2 expected from degassing of magma in the upper crust (3-6.5 km), where petrologic analysis shows the final magma equilibration occurred. Thus, the high pre-eruptive C/S ratios observed could reflect bulk degassing of upper-crustal magma followed by nearly complete loss of SO2 in a magmatic-hydrothermal system. Alternatively, high C/S ratios could be attributed to degassing of low silica andesitic magma that intruded into the mid-crust in the 5 months prior to eruption; modeling suggests that mixing of this magma with pre-existing high silica andesite magma or mush would have caused a reduction of the C/S ratio to a value consistent with that measured during the eruption. Monitoring emissions regularly

  15. Extraction and quantification of SO2 content in wines using a hollow fiber contactor.

    Science.gov (United States)

    Plaza, Andrea; Romero, Julio; Silva, Wladimir; Morales, Elizabeth; Torres, Alejandra; Aguirre, María J

    2014-10-01

    Sulfites [Formula: see text] or sulfur dioxide (SO2) is a preservative widely used in fruits and fruit-derived products. This study aims to propose a membrane contactor process for the selective removal and recovery of SO2 from wines in order to obtain its reliable quantification. Currently, the aspiration and Ripper methods offer a difficult quantification of the sulfite content in red wines because they involve evaporation steps of diluted compounds and a colorimetric assay, respectively. Therefore, an inexpensive and accurate methodology is not currently available for continuous monitoring of SO2 in the liquids food industry. Red wine initially acidified at pH membrane extraction at 25 ℃. This operation is based on a hydrophobic Hollow Fiber Contactor, which separates the acidified red wine in the shell side and a diluted aqueous sodium hydroxide solution as receiving solution into the lumenside in countercurrent. Sulfite and bisulfite in the acidified red wine become molecular SO2, which is evaporated through the membrane pores filled with gas. Thus, SO2 is trapped in a colorless solution and the membrane contactor controls its transfer, decreasing experimental error induced in classical methods. Experimental results using model solutions with known concentration values of [Formula: see text] show an average extraction percentage of 98.91 after 4 min. On the other hand, two types of Chilean Cabernet Sauvignon wines were analyzed with the same system to quantify the content of free and total sulfites. Results show a good agreement between these methods and the proposed technique, which shows a lower experimental variability. © The Author(s) 2013 Reprints and permissions: sagepub.co.uk/journalsPermissions.nav.

  16. Stomatal response of swordfern to volcanogenic CO2 and SO2 from Kilauea volcano

    Science.gov (United States)

    Tanner, Lawrence H.; Smith, David L.; Allan, Amanda

    2007-08-01

    The experimentally determined relationship between atmospheric pCO2 and plant stomata has been used to interpret large but transient changes in atmospheric composition, such as may have resulted from the eruptions of flood basalt. However, this relationship has not been tested in the field, i.e. in the vicinity of active volcanoes, to examine the specific effects of volcanogenic emissions. Moreover, the interpretation of paleoatmospheric pCO2 from fossil stomatal data assumes that the stomatal response resulted solely from variation in pCO2 and ignores the potential effect of outgassed SO2. We hypothesize that volcanogenic SO2 also has a significant effect on leaf stomata and test this hypothesis by measuring the stomatal index of the common swordfern (Nephrolepis exaltata) in the plumes of the actively outgassing vents of Kilauea volcano. We find that, compared to control locations, stomatal index is lowest at sample sites in the plume of Halema'uma'u Crater, where concentrations of both CO2 and SO2 are much higher than background. However, sites located directly in the plume of Pu'u O'o, where SO2 levels are high, but CO2 levels are not, also yield low values of stomatal index. We propose that shifts in the stomatal index of fossil leaves may record transient atmospheric increases in both SO2 and CO2, such as may be caused by eruptions of flood basalts. Calculations of pCO2 based on stomatal frequency are likely to be exaggerated.

  17. Detecting volcanic SO2 emissions with the Infrared Atmospheric Sounding Interferometer

    Science.gov (United States)

    Taylor, Isabelle; Carboni, Elisa; Mather, Tamsin; Grainger, Don

    2017-04-01

    Sulphur dioxide (SO2) emissions are one of the many hazards associated with volcanic activity. Close to the volcano they have negative impacts on human and animal health and affect the environment. Further afield they present a hazard to aviation (as well as being a proxy for volcanic ash) and can cause global changes to climate. These are all good reasons for monitoring gas emissions at volcanoes and this monitoring can also provide insight into volcanic, magmatic and geothermal processes. Advances in satellite technology mean that it is now possible to monitor these emissions from space. The Infrared Atmospheric Sounding Interferometer (IASI) on board the European Space Agency's MetOp satellites is commonly used, alongside other satellite products, for detecting SO2 emissions across the globe. A fast linear retrieval developed in Oxford separates the signal of the target species (SO2) from the spectral background by representing background variability (determined from pixels containing no SO2) in a background covariance matrix. SO2 contaminated pixels can be distinguished from this quickly, facilitating the use of this algorithm for near real time monitoring and for scanning of large datasets for signals to explore further with a full retrieval. In this study, the retrieval has been applied across the globe to identify volcanic emissions. Elevated signals are identified at numerous volcanoes including both explosive and passive emissions, which match reports of activity from other sources. Elevated signals are also evident from anthropogenic activity. These results imply that this tool could be successfully used to identify and monitor activity across the globe.

  18. Health risks of NO 2, SPM and SO 2 in Delhi (India)

    Science.gov (United States)

    Pandey, Jai Shanker; Kumar, Rakesh; Devotta, Sukumar

    There is increasingly growing evidence linking urban air pollution to acute and chronic illnesses amongst all age groups. Therefore, monitoring of ambient concentrations of various air pollutants as well as quantification of the dose inhaled becomes quite important, specially in view of the fact that in many countries, policy decisions for reducing pollutant concentrations are mainly taken on the basis of their health impacts. The dose when gets combined with the likely responses, indicates the ultimate health risk (HR). Thus, as an extension of our earlier studies, HR has been estimated for three pollutants, namely, suspended particulate matter (SPM), nitrogen dioxide (NO 2) and sulfur dioxide (SO 2) for Delhi City in India. For estimation and analyses, three zones have been considered, namely, residential, industrial and commercial. The total population has been divided into three age classes (infants, children and adults) with different body weights and breathing rates. The exercise takes into account age-specific breathing rates, body weights for different age categories and occupancy factors for different zones. Results indicate that health risks due to air pollution in Delhi are highest for children. For all age categories, health risks due to SO 2 (HR_SO 2) are the lowest. Hence, HR_SO 2 has been taken as the reference with respect to which HR values due to SPM and NO 2 have been compared. Taking into account all the age categories and their occupancy in different zones, average HR values for NO 2 and SPM turn out to be respectively 22.11 and 16.13 times more than that for SO 2. The present study can be useful in generating public awareness as well as in averting and mitigating the health risks.

  19. A global catalogue of large SO2 sources and emissions derived from the Ozone Monitoring Instrument

    Directory of Open Access Journals (Sweden)

    V. E. Fioletov

    2016-09-01

    Full Text Available Sulfur dioxide (SO2 measurements from the Ozone Monitoring Instrument (OMI satellite sensor processed with the new principal component analysis (PCA algorithm were used to detect large point emission sources or clusters of sources. The total of 491 continuously emitting point sources releasing from about 30 kt yr−1 to more than 4000 kt yr−1 of SO2 per year have been identified and grouped by country and by primary source origin: volcanoes (76 sources; power plants (297; smelters (53; and sources related to the oil and gas industry (65. The sources were identified using different methods, including through OMI measurements themselves applied to a new emission detection algorithm, and their evolution during the 2005–2014 period was traced by estimating annual emissions from each source. For volcanic sources, the study focused on continuous degassing, and emissions from explosive eruptions were excluded. Emissions from degassing volcanic sources were measured, many for the first time, and collectively they account for about 30 % of total SO2 emissions estimated from OMI measurements, but that fraction has increased in recent years given that cumulative global emissions from power plants and smelters are declining while emissions from oil and gas industry remained nearly constant. Anthropogenic emissions from the USA declined by 80 % over the 2005–2014 period as did emissions from western and central Europe, whereas emissions from India nearly doubled, and emissions from other large SO2-emitting regions (South Africa, Russia, Mexico, and the Middle East remained fairly constant. In total, OMI-based estimates account for about a half of total reported anthropogenic SO2 emissions; the remaining half is likely related to sources emitting less than 30 kt yr−1 and not detected by OMI.

  20. Effect of flue gas composition on deposit induced high temperature corrosion under laboratory conditions mimicking biomass firing. Part II: Exposures in SO2 containing atmospheres

    DEFF Research Database (Denmark)

    Okoro, Sunday Chukwudi; Kiamehr, Saeed; Montgomery, Melanie

    2017-01-01

    In biomass fired power plants, the fast corrosion of superheaters is facilitatedby the presence of corrosive flue gas species, for example, SO2, which arereleased during combustion. To understand the role of the gas species on thecorrosion process, comparative laboratory exposures of deposit (KCl......)-coatedand deposit-free austenitic stainless steel (TP 347H FG) samples to gas mixturescontaining SO2 was carried out, under conditions relevant to biomass-firing.Exposures were conducted isothermally at 560 8C for 72 h, in oxidizingsulphidizing,and oxidizing-sulphidizing-chlorinating gas mixtures containing60 ppmv...... SO2. Scanning electron microscopy (SEM), energy dispersive X-rayspectroscopy (EDS) and X-ray diffraction (XRD) techniques werecomplimentarily applied to characterize the resulting corrosion products. Apartially molten K2SO4-layer formed on KCl coated specimens, and corrosionresulted in localized...

  1. Retrieval of volcanic SO2 from HIRS/2 using optimal estimation

    Directory of Open Access Journals (Sweden)

    G. M. Miles

    2017-07-01

    Full Text Available We present an optimal-estimation (OE retrieval scheme for stratospheric sulfur dioxide from the High-Resolution Infrared Radiation Sounder 2 (HIRS/2 instruments on the NOAA and MetOp platforms, an infrared radiometer that has been operational since 1979. This algorithm is an improvement upon a previous method based on channel brightness temperature differences, which demonstrated the potential for monitoring volcanic SO2 using HIRS/2. The Prata method is fast but of limited accuracy. This algorithm uses an optimal-estimation retrieval approach yielding increased accuracy for only moderate computational cost. This is principally achieved by fitting the column water vapour and accounting for its interference in the retrieval of SO2. A cloud and aerosol model is used to evaluate the sensitivity of the scheme to the presence of ash and water/ice cloud. This identifies that cloud or ash above 6 km limits the accuracy of the water vapour fit, increasing the error in the SO2 estimate. Cloud top height is also retrieved. The scheme is applied to a case study event, the 1991 eruption of Cerro Hudson in Chile. The total erupted mass of SO2 is estimated to be 2300 kT ± 600 kT. This confirms it as one of the largest events since the 1991 eruption of Pinatubo, and of comparable scale to the Northern Hemisphere eruption of Kasatochi in 2008. This retrieval method yields a minimum mass per unit area detection limit of 3 DU, which is slightly less than that for the Total Ozone Mapping Spectrometer (TOMS, the only other instrument capable of monitoring SO2 from 1979 to 1996. We show an initial comparison to TOMS for part of this eruption, with broadly consistent results. Operating in the infrared (IR, HIRS has the advantage of being able to measure both during the day and at night, and there have frequently been multiple HIRS instruments operated simultaneously for better than daily sampling. If applied to all data from the series of past and future

  2. East Asian SO2 pollution plume over Europe – Part 2: Evolution and potential impact

    Directory of Open Access Journals (Sweden)

    A. Stohl

    2009-07-01

    Full Text Available We report on the first observation-based case study of an aged East Asian anthropogenic SO2 pollution plume over Europe. Our airborne measurements in that plume detected highly elevated SO2 mole fractions (up to 900 pmol/mol between about 5000 and 7000 m altitude. Here, we focus on investigations of the origin, dispersion, evolution, conversion, and potential impact of the observed excess SO2. In particular, we investigate SO2 conversion to gas-phase sulfuric acid and sulfuric acid aerosols. Our FLEXPART and LAGRANTO model simulations, along with additional trace gas measurements, suggest that the plume originated from East Asian fossil fuel combustion sources and, 8–7 days prior to its arrival over Europe, ascended over the coast region of central East Asia to 9000 m altitude, probably in a cyclonic system with an associated warm conveyor belt. During this initial plume ascent a substantial fraction of the initially available SO2 must have escaped from removal by cloud processes. Hereafter, while mostly descending slowly, the plume experienced advection across the North Pacific, North America and the North Atlantic. During its upper troposphere travel, clouds were absent in and above the plume and OH-induced gas-phase conversion of SO2 to gas-phase sulfuric acid (GSA was operative, followed by GSA nucleation and condensation leading to sulfuric acid aerosol formation and growth. Our AEROFOR model simulations indicate that numerous large sulfuric acid aerosol particles were formed, which at least tempora-rily, caused substantial horizontal visibility degradation, and which have the potential to act as water vapor condensation nuclei in liquid water cloud formation, already at water vapor supersaturations as low as about 0.1%. Our AEROFOR model simulations also indicate that those fossil fuel combustion generated soot particles, which have survived cloud induced removal during the initial plume ascent, have experienced extensive H2SO4/H2O

  3. A Python Software Toolbox for the Analysis of SO2 Camera Data. Implications in Geosciences

    Directory of Open Access Journals (Sweden)

    Jonas Gliß

    2017-12-01

    Full Text Available Ultraviolet (UV SO2 cameras have become a common tool to measure and monitor SO2 emission rates, mostly from volcanoes but also from anthropogenic sources (e.g., power plants or ships. Over the past decade, the analysis of UV SO2 camera data has seen many improvements. As a result, for many of the required analysis steps, several alternatives exist today (e.g., cell vs. DOAS based camera calibration; optical flow vs. cross-correlation based gas-velocity retrieval. This inspired the development of Pyplis (Python plume imaging software, an open-source software toolbox written in Python 2.7, which unifies the most prevalent methods from literature within a single, cross-platform analysis framework. Pyplis comprises a vast collection of algorithms relevant for the analysis of UV SO2 camera data. These include several routines to retrieve plume background radiances as well as routines for cell and DOAS based camera calibration. The latter includes two independent methods to identify the DOAS field-of-view (FOV within the camera images (based on (1 Pearson correlation and (2 IFR inversion method. Plume velocities can be retrieved using an optical flow algorithm as well as signal cross-correlation. Furthermore, Pyplis includes a routine to perform a first order correction of the signal dilution effect (also referred to as light dilution. All required geometrical calculations are performed within a 3D model environment allowing for distance retrievals to plume and local terrain features on a pixel basis. SO2 emission rates can be retrieved simultaneously for an arbitrary number of plume intersections. Hence, Pyplis provides a state-of-the-art framework for more efficient and flexible analyses of UV SO2 camera data and, therefore, marks an important step forward towards more transparency, reliability and inter-comparability of the results. Pyplis has been extensively and successfully tested using data from several field campaigns. Here, the main features

  4. Sulfur dioxide (SO2 from MIPAS in the upper troposphere and lower stratosphere 2002–2012

    Directory of Open Access Journals (Sweden)

    M. Höpfner

    2015-06-01

    Full Text Available Vertically resolved distributions of sulfur dioxide (SO2 with global coverage in the height region from the upper troposphere to ~20 km altitude have been derived from observations by the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS on Envisat for the period July 2002 to April 2012. Retrieved volume mixing ratio profiles representing single measurements are characterized by typical errors in the range of 70–100 pptv and by a vertical resolution ranging from 3 to 5 km. Comparison with observations by the Atmospheric Chemistry Experiment Fourier transform spectrometer (ACE-FTS revealed a slightly varying bias with altitude of −20 to 50 pptv for the MIPAS data set in case of volcanically enhanced concentrations. For background concentrations the comparison showed a systematic difference between the two major MIPAS observation periods. After debiasing, the difference could be reduced to biases within −10 to 20 pptv in the altitude range of 10–20 km with respect to ACE-FTS. Further comparisons of the debiased MIPAS data set with in situ measurements from various aircraft campaigns showed no obvious inconsistencies within a range of around ±50 pptv. The SO2 emissions of more than 30 volcanic eruptions could be identified in the upper troposphere and lower stratosphere (UTLS. Emitted SO2 masses and lifetimes within different altitude ranges in the UTLS have been derived for a large part of these eruptions. Masses are in most cases within estimations derived from other instruments. From three of the major eruptions within the MIPAS measurement period – Kasatochi in August 2008, Sarychev in June 2009 and Nabro in June 2011 – derived lifetimes of SO2 for the altitude ranges 10–14, 14–18 and 18–22 km are 13.3 ± 2.1, 23.6 ± 1.2 and 32.3 ± 5.5 days respectively. By omitting periods with obvious volcanic influence we have derived background mixing ratio distributions of SO2. At 10 km altitude these indicate an annual

  5. Ab intio Investigation of the Thermochemistry and Kinetics of the SO2 + O3− → SO3− + O2 Reaction in Aircraft Engines and the Environment

    Directory of Open Access Journals (Sweden)

    Xuechao Guo

    2014-12-01

    Full Text Available In the present work, the mechanisms, thermochemistry and kinetics of the reaction of SO2 with O3− have been studied using the CCSD(T/6-31G(d + CF method. It has been shown that there exist two possible pathways A and B of the SO2 + O3− → SO3− + O2 reaction. The two pathways’ A and B barrier heights are 0.61 kcal mol−1 and 3.40 kcal mol−1, respectively, while the energy of the SO2 + O3− → SO3− + O2 reaction is −25.25 kcal mol−1. The canonical variational transition state theory with small-curvature tunneling (CVT/SCT has been applied to study the reaction kinetics. The CVT/SCT study shows that the rate constants K for pathways A and B, KA = 1.11 × 10−12exp(−2526.13/T and KB = 2.7 × 10−14exp(−1029.25/T, respectively, grow as the temperature increases and are much larger than those of the SO2 + O3 → SO3 + O2 reaction over the entire temperature range of 200–1500 K. This indicates that ionization of O3 and high temperatures are favorable for the SO2 oxidation via the reaction with ozone. The new data obtained in the present study can be utilized directly for the evaluation of experiments and model predictions concerning SO2 oxidation and kinetic modeling of gas-phase chemistry of pollutants/nucleation precursors formed in aircraft engines and the Earth’s atmosphere.

  6. Prospects of utilization of electron beam irradiation technology to augment control of SO2 and other emissions from Chilean copper smelting plants

    International Nuclear Information System (INIS)

    Villanueva, L.; Ahumada, L.; Ellison, W.; Chmielewski, A.G.; Zimek, Z.

    1998-01-01

    Analysis of potential utilization of applicable SO 2 -removal process for reduced-SO 2 -strength off-gases, including electron-beam irradiation, for incrementally improving overall abatement of SO 2 /SO 3 emissions from existing copper smelting facilities in Chile has been carried out. Off-gases are characterized by SO 2 content higher than 3,000 ppm, a complex chemical composition and highly oxidizing conditions, along with cyclical and fluctuating generation, reflecting relatively severe service. Laboratory tests with simulated high-SO 2 -strength process gas were performed at Polish Institute of Nuclear Chemistry and Technology. Test work proved the technical feasibility of removing SO 2 from ultra-high SO 2 content smelter gases by E-beam irradiation with ammonia injection. A laboratory unit with flow rate of 20 Nm 3 /h equipped with electron accelerator of 800 keV beam energy was used. Influence of different parameters on SO 2 removal efficiency, like temperature, dose, ammonia stoichiometry and water vapor content, has been established. Tests covered a high SO 2 content range, 2,000 to 10,000 ppm. A generic design has been deviced to address system arrangement, performance and control requirements. It encompasses upgrading of in-plant ventilation to the extent required by health standards, together with gas cleaning system based on EB Process. The arrangement of the facilities provides for gathering and treating off-gas from selected fugitive emission sources on a continuous basis, at the same time in-drafting a minimum amount of tramp air. An introductory dry dedusting stage uses activated coke injection in conjunction with a fabric filter to efficiently treat raw gas to remove heavy metals, including arsenic, along with particulate matter. Main conclusion of the two major stages of this work, i.e. experimental tests and engineering oriented studies, is that the EB Process is a simple and appropriate, cost-effective, chemical process that would, on a site

  7. Numerical Model of SO2 Scrubbing with Seawater Applied to Marine Engines

    Directory of Open Access Journals (Sweden)

    Lamas M. I.

    2016-04-01

    Full Text Available The present paper proposes a CFD model to study sulphur dioxide (SO2 absorption in seawater. The focus is on the treatment of marine diesel engine exhaust gas. Both seawater and distilled water were compared to analyze the effect of seawater alkalinity. The results indicate that seawater is more appropriate than distilled water due to its alkalinity, obtaining almost 100% cleaning efficiency for the conditions analyzed. This SO2 reduction meets the limits of SOx emission control areas (SECA when operating on heavy fuel oil. These numerical simulations were satisfactory validated with experimental tests. Such data are essential in designing seawater scrubbers and judging the operating cost of seawater scrubbing compared to alternative fuels.

  8. The US SO2 AUCTION: A policy recommendation for future auctions

    International Nuclear Information System (INIS)

    Christensen, J.L.; Thinggaard Svendsen, G.

    1998-01-01

    An annual discriminative and revenue-neutral auction is linked to the new Acid Rain Program which allows electric utilities all over the US to trade SO2 emission permits. This innovative SO2 auction distributes 2% of the permits in circulation and takes place at the Chicago Board of Trade. Early results showed that the auction generated a clearing price signal lower than the market price. Now the auction price seems to be determined by the outside market price. Still, in the important starting phase, a non-discriminative auction design would probably have generated better price signals since potentially severe downward biases in both seller price offers and buyer bids are due to the discriminative feature of the EPA auction. (au) 30 refs

  9. Land use patterns and SO2 and NO2 pollution in Ulaanbaatar, Mongolia.

    Science.gov (United States)

    Huang, Yu-Kai; Luvsan, Munkh-Erdene; Gombojav, Enkhjargal; Ochir, Chimedsuren; Bulgan, Jargal; Chan, Chang-Chuan

    2013-07-01

    We proposed to study spatial distribution and source contribution of SO2 and NO2 pollution in Ulaanbaatar, Mongolia. We collected 2-week ambient SO2 and NO2 concentration samples at 38 sites, which were classified by major sources of air pollution such as ger areas and/or major roads, in three seasons as warm (September, 2011), cold (November-December, 2011), and moderate (March, 2012) in Ulaanbaatar. The SO2 and NO2 concentrations were collected by Ogawa ambient air passive samplers and analyzed by ion chromatography and spectrophotometry methods, respectively. Stepwise regression models were used to estimate the contribution of emission proxies, such as the distance to major roads, ger areas, power plants, and city center, to the ambient concentrations of SO2 and NO2. We found that the SO2 and NO2 concentrations were significantly higher in the cold season than in the warm and moderate seasons at all 38 ambient sampling sites. The SO2 concentrations in 20 ger sites (46.60 ppb in the cold season and 17.82 ppb in the moderate season) were significantly higher than in 18 non-ger sites (23.35 ppb in the cold season and 12.53 ppb in the moderate season). The NO2 concentrations at 19 traffic/road sites (12.85 ppb in the warm season and 20.48 ppb in the moderate season) were significantly higher than those at 19 urban sites (7.60 ppb and 14.39 ppb in the moderate season). Multiple regression models show that SO2 concentrations decreased by 23% in the cold and 17% in the moderate seasons at 0.70 km from the ger areas, an average of all sampling sites, and by 29% in the moderate season at 4.83 km from the city center, an average of all sampling sites. Multiple regression models show that the NO2 concentrations at 4.83 km from the city center decreased by 38% in the warm and 29% in the moderate seasons. Our models also report that NO2 concentrations at 0.16 km from the main roads decreased by 15% and 9% in the warm and the moderate seasons, respectively, and by 16% in the

  10. Effects of SO2-fumigation on the infection of Norway spruce by Armillaria ostoyae

    International Nuclear Information System (INIS)

    Horak, M.; Tesche, M.

    1993-01-01

    SO 2 fumigation (0.86 mg/m 3 ) reduced drastically the survival expectancy of spruce seedlings already after 1 month. Under such conditions, the infection of spruce by Armillaria ostoyae is known to increase. The present investigation has shown that mortality increased strongly by combining A. ostoyae infection and fumigation. However, mycorrhization of spruce (Paxillus involutus) increased the survival rate of seedlings and reduced infection by A. ostoyae remarkably (20%). (orig.) [de

  11. A novel CO2- and SO2-tolerant dual phase composite membrane for oxygen separation

    DEFF Research Database (Denmark)

    Cheng, Shiyang; Søgaard, Martin; Han, Li

    2015-01-01

    A novel dual phase composite oxygen membrane (Al0.02Ga0.02Zn0.96O1.02 – Gd0.1Ce0.9O1.95-δ) was successfully prepared and tested. The membrane shows chemical stability against CO2 and SO2, and a stable oxygen permeation over 300 hours in CO2 was demonstrated. ZnO is cheap and non...

  12. Continuation of long-term global SO2 pollution monitoring from OMI to OMPS

    Science.gov (United States)

    Zhang, Yan; Li, Can; Krotkov, Nickolay A.; Joiner, Joanna; Fioletov, Vitali; McLinden, Chris

    2017-04-01

    Over the past 20 years, advances in satellite remote sensing of pollution-relevant species have made space-borne observations an increasingly important part of atmospheric chemistry research and air quality management. This progress has been facilitated by advanced UV-vis spectrometers, such as the Ozone Monitoring Instrument (OMI) on board the NASA Earth Observing System (EOS) Aura satellite, and continues with new instruments, such as the Ozone Mapping and Profiler Suite (OMPS) on board the NASA-NOAA Suomi National Polar-orbiting Partnership (SNPP) satellite. In this study, we demonstrate that it is possible, using our state-of-the-art principal component analysis (PCA) retrieval technique, to continue the long-term global SO2 pollution monitoring started by OMI with the current and future OMPS instruments that will fly on the NOAA Joint Polar Satellite System (JPSS) 1, 2, 3, and 4 satellites in addition to SNPP, with a very good consistency of retrievals from these instruments. Since OMI SO2 data have been primarily used for (1) providing regional context on air pollution and long-range transport on a daily basis and (2) providing information on point emission sources on an annual basis after data averaging, we focused on these two aspects in our OMI-OMPS comparisons. Four years of retrievals (2012-2015) have been compared for three regions: eastern China, Mexico, and South Africa. In general, the comparisons show relatively high correlations (r = 0. 79-0.96) of daily regional averaged SO2 mass between the two instruments and near-unity regression slopes (0.76-0.97). The annual averaged SO2 loading differences between OMI and OMPS are small (used.

  13. Heat generation in lithium-thionyl chloride and lithium-SO2 cells

    Science.gov (United States)

    Cohen, R.; Melman, A.; Livne, N.; Peled, E.

    1992-09-01

    The effects of current density, temperature, depth of discharge (DOD), and storage on the heat generation rate and faradaic efficiency of Li/Tc and Li/SO2 cells have been determined. Several C-size commercial cells from different manufacturers have been tested. The faradaic efficiency for both systems was found to be very high, typically 96-100 percent even at high current density and high temperatures (55 C). It does not change much with DOD and decreases only slightly with the increase of current density and high temperature (tested up to 4.5 mA/sq cm at 50 percent DOD and 55 C). A performance degradation problem was found for some Li/TC cells. The heat factor, the ratio between the useful electric power and the thermal power generated by the cell, is about the same for fresh Li/TC cells and Li/SO2 cells. However, some Li/TC cells stored for 3 years showed a poor heat factor. It was confirmed that the maximum thermoneutral voltage for the Li/TC and Li/SO2 cells is 3.80 and 3.22 V, respectively.

  14. Lignite-fired thermal power plants and SO2 pollution in Turkey

    International Nuclear Information System (INIS)

    Say, Nuriye Peker

    2006-01-01

    About 80% of the electric energy production in Turkey is provided by thermal power plants which use fossil fuels. Lignite, the most abundant domestic energy source, is consumed in most of these plants. Turkey has approximately 0.85% of the world's lignite reserves; however, the Turkish lignites have low calorific value and contain relatively higher amounts of ash, moisture, and sulfur. Nearly 80% of the lignite mined in Turkey is consumed in the thermal power plants since it is not appropriate for use in other types of industry and heating. In Turkey, 13 large-scale lignite-fired thermal power plants are responsible for a considerable amount of air pollution. Therefore, it is crucial to decide on the optimal place and technology for the future thermal power plants, and to equip the currently operating plants with newer technologies that will reduce amount of contaminants released into the air. In this study, the effects of the lignite-fired thermal power plants which have an important place in the energy politics in Turkey on the air pollution are investigated. We focused on SO 2 pollution and the regions in which the SO 2 emissions were concentrated and diffused. The pollutant diffusion areas were projected and mapped based on parameters such as wind data, isotherm curves, population density, and topographic features by using Geographical Information System (GIS) software, ArcView. The contribution of the thermal power plants to SO 2 pollution was also examined

  15. Sodium bicarbonate in-duct injection with sodium sulfate recovery for SO2/NOx control

    International Nuclear Information System (INIS)

    Bennett, R.; Darmstaedter, E.

    1991-01-01

    Dry sodium injection with sodium bicarbonate has been used commercially at industrial sites since the mid 1980's. In the past three years, five full scale commercial demonstrations have been completed on electric utility coal fired units. Up to 75% SO 2 removal with 0-40% NO x removal has been achieved on units equipped with ESPs. Recent slip stream studies have proven up to 90% SO 2 removal and 25% NO x removal when injection is ahead of a baghouse. If dry sodium bicarbonate sorbent injection technology is used prior to a retrofitted baghouse, but after an existing ESP the sodium sulfate by-product/flyash mixture in the baghouse is over 90% Na 2 SO 4 . Simple filtration and crystallization will yield a high value 99% + pure Na 2 SO 4 for sale. In this application, no liquid discharge occurs and potentially no solids discharge, since flyash recovered from the filter is either recycled to the boiler with the coal stream or reinjected into the boiler. EPA IAPCS model Version 4 is modified to project costs for this SO 2 /NO x removal technology when couples with Na 2 SO 4 recovery. In this paper an example is used to show hardware requirements, consumables accountability, by-product recovery rates, capital costs and levelized costs

  16. Rate constant for the reaction SO + BrO yields SO2 + Br

    Science.gov (United States)

    Brunning, J.; Stief, L.

    1986-01-01

    The rate of the radical-radical reaction SO + BrO yields SO2 + Br has been determined at 298 K in a discharge flow system near 1 torr pressure with detection of SO and BrO via collision-free sampling mass spectrometry. The rate constant was determined using two different methods: measuring the decay of SO radicals in the presence of an excess of BrO and measuring the decay of BrO radicals in excess SO. The results from the two methods are in reasonable agreement and the simple mean of the two values gives the recommended rate constant at 298 K, k = (5.7 + or - 2.0) x 10 to the -11th cu cm/s. This represents the first determination of this rate constant and it is consistent with a previously derived lower limit based on SO2 formation. Comparison is made with other radical-radical reactions involving SO or BrO. The reaction SO + BrO yields SO2 + Br is of interest for models of the upper atmosphere of the earth and provides a potential coupling between atmospheric sulfur and bromine chemistry.

  17. OMPS/NPP PCA SO2 Total Column 1-Orbit L2 Swath 50x50km NRT

    Data.gov (United States)

    National Aeronautics and Space Administration — The OMPS-NPP L2 NM Sulfur Dioxide (SO2) Total and Tropospheric Column swath orbital collection 2 version 2.0 product contains the retrieved sulfur dioxide (SO2)...

  18. Sulfur Isotopic Fractionation During Vacuum Ultraviolet Photolysis of SO2: Implication for Meteorites and Early Earth

    Science.gov (United States)

    Chakraborty, S.; Jackson, T. L.; Rude, B.; Ahmed, M.; Thiemens, M. H.

    2016-12-01

    Several sulfur bearing gas phase species existed in the solar nebula, including H2S, SO2, SiS, OCS, CS2, CS, NS and SO as a consequence of multiple available chemical valence states (S2- to S6+). Sulfur directly condensed into refractory phases in the solar nebula under reducing conditions. Mass independent (MI) sulfur isotopic compositions have been measured in chondrules and organics from chondritic meteorites. Large 33S excesses in sulfides from achondrite meteoritic groups have also been found suggesting that refractory sulfide minerals condensed from a nebular gas with an enhanced carbon to oxygen ratio. Photochemical reactions in the early solar nebula have been inferred to be a leading process in generating MI sulfur compositions. Previously, we have reported wavelength dependent mass-independent sulfur isotopic compositions (with a varying degree in D33S and D36S) in the product elemental sulfur during vacuum ultraviolet (VUV) photodissociation of H2S. Recently we performed photodissociation of SO2 experiments in the wavelength region 98 to 200 nm at low pressures (0.5 torr) using the VUV photons from the Advanced Light Source Synchrotron in a differentially pumped reaction chamber. To our knowledge, this is the first ever experiment to determine the isotopic fractionation in VUV photodissociation of SO2. At VUV energy region, SO2 is mostly predissociative. The measured sulfur isotopic compositions in the product elemental sulfur are MI and dependent on the wavelength. These new results support the previous finding from photodissociation of other di- and tri-atomic molecules (CO, N2, H2S) that predissociative photodissociation produces MI isotopic products and is a quantum mechanically driven selective phenomenon. These new results are useful because (i) they are important in interpreting meteoritic data and decipher sulfur chemistry in the early nebula which is indicative of the redox condition of the nebula (ii) SO2 photolysis in the atmosphere of early

  19. 40 CFR 75.33 - Standard missing data procedures for SO2, NOX, Hg, and flow rate.

    Science.gov (United States)

    2010-07-01

    ... SO2, NOX, Hg, and flow rate. 75.33 Section 75.33 Protection of Environment ENVIRONMENTAL PROTECTION... Procedures § 75.33 Standard missing data procedures for SO2, NOX, Hg, and flow rate. (a) Following initial...—Missing Data Procedure for SO2 CEMS, CO2 CEMS, Moisture CEMS, Hg CEMS, and Diluent (CO2 or O2) Monitors...

  20. Effects of NOx and SO2 on the secondary organic aerosol formation from photooxidation of α-pinene and limonene

    Science.gov (United States)

    Zhao, Defeng; Schmitt, Sebastian H.; Wang, Mingjin; Acir, Ismail-Hakki; Tillmann, Ralf; Tan, Zhaofeng; Novelli, Anna; Fuchs, Hendrik; Pullinen, Iida; Wegener, Robert; Rohrer, Franz; Wildt, Jürgen; Kiendler-Scharr, Astrid; Wahner, Andreas; Mentel, Thomas F.

    2018-02-01

    Anthropogenic emissions such as NOx and SO2 influence the biogenic secondary organic aerosol (SOA) formation, but detailed mechanisms and effects are still elusive. We studied the effects of NOx and SO2 on the SOA formation from the photooxidation of α-pinene and limonene at ambient relevant NOx and SO2 concentrations (NOx: biogenic volatile organic compounds (VOCs) with anthropogenic emissions.

  1. Lyman Alpha Camera for Io's SO2 atmosphere and Europa's water plumes

    Science.gov (United States)

    McEwen, Alfred S.; Sandel, Bill; Schneider, Nick

    2014-05-01

    The Student Lyman-Alpha Mapper (SLAM) was conceived for the Io Volcano Observer (IVO) mission proposal (McEwen et al., 2014) to determine the spatial and temporal variations in Io's SO2 atmosphere by recording the H Ly-α reflection over the disk (Feldman et al., 2000; Feaga et al., 2009). SO2 absorbs at H Ly-α, thereby modulating the brightness of sunlight reflected by the surface, and measures the density of the SO2 atmosphere and its variability with volcanic activity and time of day. Recently, enhancements at the Ly-α wavelength (121.57 nm) were seen near the limb of Europa and interpreted as active water plumes ~200 km high (Roth et al., 2014). We have a preliminary design for a very simple camera to image in a single bandpass at Ly-α, analogous to a simplified version of IMAGE EUV (Sandel et al. 2000). Our goal is at least 50 resolution elements across Io and/or Europa (~75 km/pixel), ~3x better than HST STIS, to be acquired at a range where the radiation noise is below 1E-4 hits/pixel/s. This goal is achieved with a Cassegrain-like telescope with a 10-cm aperture. The wavelength selection is achieved using a simple self-filtering mirror in combination with a solar-blind photocathode. A photon-counting detector based on a sealed image intensifier preserves the poisson statistics of the incoming photon flux. The intensifier window is coated with a solar-blind photocathode material (CsI). The location of each photon event is recorded by a position-sensitive anode based on crossed delay-line or wedge-and-strip technology. The sensitivity is 0.01 counts/pixel/sec/R, sufficient to estimate SO2 column abundances ranging from 1E15 to 1E17 per cm2 in a 5 min (300 sec) exposure. Sensitivity requirements to search for and image Europa plumes may be similar. Io's Ly-α brightness of ~3 kR exceeds the 0.8 kR brightness of Europa's plume reported by Roth et al. (2014), but the plume brightness is a direct measurement rather than inferring column abundance from

  2. Regional and Global Climate Response to Anthropogenic SO2 Emissions from China in Three Climate Models

    Science.gov (United States)

    Kasoar, M.; Voulgarakis, Apostolos; Lamarque, Jean-Francois; Shindell, Drew T.; Bellouin, Nicholas; Collins, William J.; Faluvegi, Greg; Tsigaridis, Kostas

    2016-01-01

    We use the HadGEM3-GA4, CESM1, and GISS ModelE2 climate models to investigate the global and regional aerosol burden, radiative flux, and surface temperature responses to removing anthropogenic sulfur dioxide (SO2) emissions from China. We find that the models differ by up to a factor of 6 in the simulated change in aerosol optical depth (AOD) and shortwave radiative flux over China that results from reduced sulfate aerosol, leading to a large range of magnitudes in the regional and global temperature responses. Two of the three models simulate a near-ubiquitous hemispheric warming due to the regional SO2 removal, with similarities in the local and remote pattern of response, but overall with a substantially different magnitude. The third model simulates almost no significant temperature response. We attribute the discrepancies in the response to a combination of substantial differences in the chemical conversion of SO2 to sulfate, translation of sulfate mass into AOD, cloud radiative interactions, and differences in the radiative forcing efficiency of sulfate aerosol in the models. The model with the strongest response (HadGEM3-GA4) compares best with observations of AOD regionally, however the other two models compare similarly (albeit poorly) and still disagree substantially in their simulated climate response, indicating that total AOD observations are far from sufficient to determine which model response is more plausible. Our results highlight that there remains a large uncertainty in the representation of both aerosol chemistry as well as direct and indirect aerosol radiative effects in current climate models, and reinforces that caution must be applied when interpreting the results of modelling studies of aerosol influences on climate. Model studies that implicate aerosols in climate responses should ideally explore a range of radiative forcing strengths representative of this uncertainty, in addition to thoroughly evaluating the models used against

  3. Ozone variations related to volcanic activity and disappearance of SO2

    Science.gov (United States)

    Roldugin, V. C.; Henriksen, K.

    The long-term trend analysis of the total ozone data for the period 1973-1989 was made for three regions of the USSR. A common negative trend is explained by the eruptions of Fuego and El Chichon as one of two considered reasons, and comparison of the ozone and sulphur dioxide data for Murmansk gives further evidence to the study of De Muer and De Backer, finding that an ozone decrease vanishes when correction for tropospheric SO2 decrease is carried out. The well-known hypothesis about anthropogenic induced depletion of the ozone layer is not confirmed by these data.

  4. Feulgen type staining of mammalian tissues with Dahlia-SO2.

    Science.gov (United States)

    Dutt, M K

    1977-01-01

    The use of the basic dye, Dahlia, which belongs to triphenylmethane group but without a primary amino group in its molecule has been described as useful in the staining of aldehyde groups of acid hydrolysed DNA in tissue sections following the conventional Feulgen procedure. Dahlia-SO2 prepared with sodium hydrosulphite is highly suitable when used at pH 4-0 to 5-0. The absorption characteristics of the stained nuclei indicate on the peak of maximum absorption at 560 nm, whereas, that of the aqueous dye solution is at 590 nm.

  5. Formaldehyde and its relation to CO, PAN, and SO2 in the Houston-Galveston airshed

    Directory of Open Access Journals (Sweden)

    Q. Li

    2010-03-01

    Full Text Available The Houston-Galveston Airshed (HGA is one of the major metropolitan areas in the US that is classified as a nonattainment area of federal ozone standards. Formaldehyde (HCHO is a key species in understanding ozone related air pollution; some of the highest HCHO concentrations in North America have been reported for the HGA. We report on HCHO measurements in the HGA from summer 2006. Among several sites, maximum HCHO mixing ratios were observed in the Houston Ship Channel (HSC, a region with a very high density of industrial/petrochemical operations. HCHO levels at the Moody Tower (MT site close to downtown were dependent on the wind direction: southerly maritime winds brought in background levels (0.5–1 ppbv while trajectories originating in the HSC resulted in high HCHO (up to 31.5 ppbv. Based on the best multiparametric linear regression model fit, the HCHO levels at the MT site can be accounted for as follows: 38.5±12.3% from primary vehicular emissions (using CO as an index of vehicular emission, 24.1±17.7% formed photochemically (using peroxyacetic nitric anhydride (PAN as an index of photochemical activity and 8.9±11.2% from industrial emissions (using SO2 as an index of industrial emissions. The balance 28.5±12.7% constituted the residual which cannot be easily ascribed to the above categories and/or which is transported into the HGA. The CO related HCHO fraction is dominant during the morning rush hour (06:00–09:00 h, all times are given in CDT; on a carbon basis, HCHO emissions are up to 0.7% of the CO emissions. The SO2 related HCHO fraction is significant between 09:00–12:00 h. After 12:00 h HCHO is largely formed through secondary processes. The HCHO/PAN ratios are dependent on the SO2 levels. The SO2 related HCHO fraction at the downtown site originates in the ship channel. Aside from traffic-related primary HCHO emissions, HCHO of industrial origin serves as an appreciable source for OH in the morning.

  6. Modelling of limestone injection for SO2 capture in a coal fired utility boiler

    International Nuclear Information System (INIS)

    Kovacik, G.J.; Reid, K.; McDonald, M.M.; Knill, K.

    1997-01-01

    A computer model was developed for simulating furnace sorbent injection for SO 2 capture in a full scale utility boiler using TASCFlow TM computational fluid dynamics (CFD) software. The model makes use of a computational grid of the superheater section of a tangentially fired utility boiler. The computer simulations are three dimensional so that the temperature and residence time distribution in the boiler could be realistically represented. Results of calculations of simulated sulphur capture performance of limestone injection in a typical utility boiler operation were presented

  7. Lichens as bioindicators of air pollution by SO2 in the Veneto Region

    OpenAIRE

    Nimis, P.L.; Lazzarin, G.; Gasparo, D.

    2017-01-01

    This paper presents the results of a study on air pollution by SO2 in the Veneto Region (North Eastern Italy), using the "Calibrated Lichen lndex of Air Quality" (I.A.P.) proposed by Liebendoerfer et al. (1988). This index, based on the frequency of epiphytic lichen species within a sampling grid of 10 units, has been tested by the authors in two preliminary studies carried out in two different areas of Northern ltaly (the town of La Spezia and the northern part of the province of Vicenza), r...

  8. The Relationship Between Emissions and Economic Growth for SO2, CO2, and BC

    Science.gov (United States)

    Ru, M.; Shindell, D. T.; Tao, S.; Zhong, Q.; Seltzer, K.

    2017-12-01

    We characterize the relationship between per person emissions of SO2, CO2, and black carbon (BC) and income using a global country-level emission inventory. Pollutant emissions of SO2 and BC from the power, industry, and transportation sectors largely follow an Environmental Kuznets Curve (EKC) pattern with peak emissions at income levels between 10,000 and 100,000 USD per capita. However, for CO2, any estimated turnover income is extremely high and unlikely to be reached in the near future in power, industry, and transportation. Residential emissions show a negatively sloped linear relationship for BC, a small positive slope for CO2, and a fairly flat trajectory for SO2. For the EKC-like trajectories, "turning point" incomes for each sector and pollutant are related to technological advances and the effectiveness of emission controls. These results suggest that policy targeting technological advances and emission controls could change future pathways by affecting the "turning point" incomes. For the linear trajectories in the residential sector, we show that transitions from biomass fuel to coal in low-income countries and from coal to natural gas in middle and high-income countries, in concert with electrification levels, are the main factors governing slopes. Thus, the three pollutants show different income-emission trajectories based on the sum of the four major sectors, and the residential sector in particular has a unique relationship with income growth. As one of the first studies to analyze historical emission trajectories of BC, we find that BC differs from SO2 and CO2 because of its significantly earlier turnover in the power and industry sectors due to control policies. Total BC emissions trajectories follow a unique shape due to the combination of linearly decreasing residential emissions with EKC-like patterns in industry and transportation. We compare these trajectories to those in three Integrated Assessment Models (IAMs), GCAM, AIM, and MESSAGE

  9. Quantitative observation of boundary-layer NO2/SO2 from total-column measurements. New possibilities for space-based observations?

    Science.gov (United States)

    Knepp, T.; Pippin, M. R.; Cowen, L.; Murray, J.; Fishman, J.; Neil, D. O.; Martin, R.; Sorkin, A.; Jennings, T.; Szykamn, J.; Martins, D. K.; Thompson, A. M.; Stauffer, R. M.; Herman, J. R.; Cede, A.; Abuhassan, N.

    2011-12-01

    NO2 and SO2 are criteria pollutants that play key roles in the formation of O3 and particulate matter. NO2 is significantly associated with mortality, has far reaching effects on crop yield/photosynthesis (Fishman et al. 2010), atmospheric oxidative capacity, and radiation balance either directly or via its role in ozone/radical chemistry. Major sources of NOx (NO + NO2) and SO2 include motor vehicles, power plants, fossil fuel combustion, burning biomass fuel, and natural sources (e.g. wildfires and volcanoes). GEO-CAPE (Geostationary Coastal and Air Pollution Events mission) will be in a geo-stationary orbit over the United States with improved resolution allowing observation of hourly city-scale emissions. However, estimation of surface NO2/SO2 from total-column data is complicated due to meteorological dynamics and dimensional incongruities. NASA's Chemistry And Physics of the Atmospheric Boundary Layer Experiment (CAPABLE; Langley Research Center, Hampton VA) was established to improve our understanding of these relationships. Collocated at CAPABLE are a direct-sun spectrometer (Pandora), which has previously been shown to have good agreement with OMI's NO2 retrieval, from which column NO2 and SO2 are retrieved with two-minute resolution, and surface NO2/SO2 instruments. Using the EDAS40 model for mixed-depth height we present a methodology for estimating surface NO2 from column observations that accounts for approximately 75% of the variability. Furthermore, Pandora is capable of detecting SO2 emissions from a small power plant approximately 10km NNE of the site, while OMI consistently detects no change in its corresponding pixel. Herein we present our methodology and discuss its applicability to future remote sensing missions and space-based emissions monitoring/regulation.

  10. Enhancement of removal of SO2 and NOx by powdery materials in radiation treatment of exhaust gases

    International Nuclear Information System (INIS)

    Tokunaga, Okihiro; Namba, Hideki; Suzuki, Nobutake

    1985-01-01

    We studied the effect of powdery silica on radiation removal of SO 2 and NOx from mixtures of SO 2 , NOx, water vapour, oxygen and nitrogen under irradiation by electron beams of 1.5 MeV at 120 0 C. The SO 2 and NOx concentrations decreased when powdery silica was fed without irradiation. Decrements of SO 2 and NOx concentrations were markedly enhanced when powdery silica was fed together with the irradiation. The enhancement of SO 2 - and NOx-removal is attributed to the adsorption of SO 2 and NO on the water-covered surface of powdery silica, and the effective removal of NO 2 due to the reaction with water adsorbed on the surface of powdery silica. The results obtained show that the addition of powdery silica under irradiation is an effective method of enhancing the removal of SO 2 and NOx. (author)

  11. Acidic gases (CO2, NO2 and SO2) capture and dissociation on metal decorated phosphorene

    Science.gov (United States)

    Kuang, Anlong; Kuang, Minquan; Yuan, Hongkuan; Wang, Guangzhao; Chen, Hong; Yang, Xiaolan

    2017-07-01

    Density functional theory is employed to investigate the adsorption and dissociation of several acidic gases (CO2, NO2 and SO2) on metal (Li, Al, Ni and Pt) decorated phosphorene. The results show that light metal (Li, Al) decorated phosphorene exhibits a strong adsorption of acidic gases, i.e., the adsorption energy of CO2 on Li decorated phosphorene is 0.376 eV which is the largest in all adsorption of CO2 on metal decorated phosphorene and Al decorated phosphorene is most effective for capture of NO2 and SO2 due to large adsorption energies of 3.951 and 3.608 eV, respectively. Moreover, Li and Al light metals have stronger economic effectiveness and more friendly environment compared with the transition metals, the strong adsorption ability of acidic gases and low price suggest that Li, Al decorated phosphorene may be useful and promising for collection and filtration of exhaust gases. The reaction energy barriers of acidic gases dissociated process on Pt decorated phosphorene are relatively low and the reaction processes are significantly exothermic, indicating that the dissociation process is favorable.

  12. Quantifying the direct effects of SO2 and O3 on forest growth

    International Nuclear Information System (INIS)

    Mohren, G.M.J.; Jorritsma, I.T.M.; Vermetten, A.W.M.; Kropff, M.J.; Smeets, W.L.M.; Tiktak, A.

    1992-01-01

    The direct effects of sulphur dioxide (SO 2 ) and ozone (O 3 ) on the growth of two Douglas-fir stands are quantified from continuous measurements of the concentration of air pollution above the canopy combined with a quantitative description of the direct effects of gaseous uptake of pollutants on photosynthesis and respiration. Effects at the leaf level are scaled up to the stand level, using a deterministic model of forest growth that uses time steps of 1 day. This approach enables total uptake of gaseous air pollutants and their effects on canopy assimilation and growth to be quantified, taking ambient weather conditions and stand structure into account. By using a description of water balance in the model, the influence of limitations in oil moisture availability can also be incorporated, and the combined effects of air pollution and water shortage can be accounted for. Under Dutch conditions, with average daily concentrations of 10 μg m -1 for SO 2 and 50 μg m -3 for O 3 , the short-term effects on tree growth appear to be minor, except near local sources, and during episodes of high concentrations under stable weather conditions. The possible magnitude of long-term effects of exposure to O 3 is assessed using a hypothetical relationship between dose (exposure multiplied by duration) and foliage loss. From this it is concluded that long-term effects may be significant in stands with a low leaf area index

  13. Correlation of SO2 Gas Emissions, Seismicity and Thermal Signals at Santiaguito, Guatemala

    Science.gov (United States)

    Branan, Y. K.; Watson, I.; Harris, A. J.; Rose, W.; Bluth, G. J.; Chigna, G.; Mota, M.

    2003-12-01

    With vertical explosions occurring approximately every 40-50 minutes, the Santiaguito dome at Santa Maria Volcano is an ideal system for examining short-term data patterns. A 3-week long field experiment was performed in January 2003 at the Santiaguito Volcano Observatory in order to record high temporal resolution measurements of volcanic activity. We collected digital seismic data from a single vertical component seismometer located approximately 4 km southeast of the active Caliente vent. A portable infrared thermal monitoring unit was deployed daily to record the temperature of the plume as it left the vent at an acquisition rate of 300 measurements per minute. A miniature ultraviolet spectrometer (MUSE) was also deployed daily to measure the SO2 gas emissions just above the vent. This instrument is based on the differential optical absorption spectroscopy (DOAS) technique and allowed for continuous readings at a rate of 36 measurements per minute from approximately 6.5 km south of the Caliente vent. At abstract time, the seismic data is not analyzed, but there is a strong correlation between the SO2 emission and thermal data showing that the expulsed gas heats the dome extensively as it is emitted, with a possibility of different signatures indicating certain types of activity such as pyroclastic flows. It is expected that, with the addition of seismic data and the application of analysis of periodicity using Fourier Transforms, the data will elucidate conduit processes, providing additional vital constraints to sub-surface models.

  14. A field evaluation of a SO 2 passive sampler in tropical industrial and urban air

    Science.gov (United States)

    Cruz, Lícia P. S.; Campos, Vânia P.; Silva, Adriana M. C.; Tavares, Tania M.

    Passive samplers have been widely used for over 30 years in the measurement of personal exposure to vapours and gases in the workplace. These samplers have just recently been applied in the monitoring of ambient air, which presents concentrations that are normally much smaller than those found in occupational environments. The locally constructed passive sampler was based on gas molecular diffusion through static air layer. The design used minimizes particle interference and turbulent diffusion. After exposure, the SO 2 trapped in impregnated filters with Na 2CO 3 was extracted by means of an ultrasonic bath, for 15 min, using 1.0×10 -2 mol L -1 H 2O 2. It was determined as SO 4-2 by ion chromatography. The performance of the passive sampler was evaluated at different exposure periods, being applied in industrial and urban areas. Method precision as relative standard deviation for three simultaneously applied passive samplers was within 10%. Passive sampling, when compared to active monitoring methods under real conditions, used in urban and industrial areas, showed an overall accuracy of 15%. A statistical comparison with an active method was performed to demonstrate the validity of the passive method. Sampler capacity varied between 98 and 421 μg SO 2 m -3 for exposure periods of one month and one week, respectively, which allows its use in highly polluted areas.

  15. Reduction of sulphate content from coated alumina SO 2+ 4 Al 2 O 3 ...

    African Journals Online (AJOL)

    The aim of this study was to reduce the anion (sulphate) content from such· oxide layer wing spillover phenomena. Three catalysts were used for this purpose as a spillover hydrogen generator. From the three used catalysts PdlAIPJ is the only catalyst that can reduce anion from this oxide layer:. The result showed the ...

  16. Ship emissions of SO2 and NO2: DOAS measurements from airborne platforms

    Directory of Open Access Journals (Sweden)

    J.-P. Jalkanen

    2012-05-01

    Full Text Available A unique methodology to measure gas fluxes of SO2 and NO2 from ships using optical remote sensing is described and demonstrated in a feasibility study. The measurement system is based on Differential Optical Absorption Spectroscopy using reflected skylight from the water surface as light source. A grating spectrometer records spectra around 311 nm and 440 nm, respectively, with the telescope pointed downward at a 30° angle from the horizon. The mass column values of SO2 and NO2 are retrieved from each spectrum and integrated across the plume. A simple geometric approximation is used to calculate the optical path. To obtain the total emission in kg h−1 the resulting total mass across the plume is multiplied with the apparent wind, i.e. a dilution factor corresponding to the vector between the wind and the ship speed. The system was tested in two feasibility studies in the Baltic Sea and Kattegat, from a CASA-212 airplane in 2008 and in the North Sea outside Rotterdam from a Dauphin helicopter in an EU campaign in 2009. In the Baltic Sea the average SO2 emission out of 22 ships was (54 ± 13 kg h−1, and the average NO2 emission was (33 ± 8 kg h−1, out of 13 ships. In the North Sea the average SO2 emission out of 21 ships was (42 ± 11 kg h−1, NO2 was not measured here. The detection limit of the system made it possible to detect SO2 in the ship plumes in 60% of the measurements when the described method was used. A comparison exercise was carried out by conducting airborne optical measurements on a passenger ferry in parallel with onboard measurements. The comparison shows agreement of (−30 ± 14% and (−41 ± 11%, respectively, for two days, with equal measurement precision of about 20%. This gives an idea of the measurement uncertainty caused by errors in the simple geometric approximation for the optical light path neglecting scattering of the light in ocean waves and direct and multiple scattering in the exhaust plume under

  17. Trust management in cloud services

    CERN Document Server

    Noor, Talal H; Bouguettaya, Athman

    2014-01-01

    This book describes the design and implementation of Cloud Armor, a novel approach for credibility-based trust management and automatic discovery of cloud services in distributed and highly dynamic environments. This book also helps cloud users to understand the difficulties of establishing trust in cloud computing and the best criteria for selecting a service cloud. The techniques have been validated by a prototype system implementation and experimental studies using a collection of real world trust feedbacks on cloud services.The authors present the design and implementation of a novel pro

  18. Response of SO2 and Particulate Air Pollution to Local and Regional Emission Controls: A Case Study in Maryland

    Science.gov (United States)

    He, Hao; Vinnikov, Konstantin Y.; Li, Can; Krotkov, Nickolay Anatoly; Jongeward, Andrew R.; Li, Zhanqing; Stehr, Jeffrey W.; Hains, Jennifer; Dickerson, RUssell R.

    2016-01-01

    This paper addresses the questions of what effect local regulations can have on pollutants with different lifetimes and how surface observations and remotely sensed data can be used to determine the impacts. We investigated the decadal trends of tropospheric sulfur dioxide (SO2) and aerosol pollution over Maryland and its surrounding states, using surface, aircraft, and satellite measurements. Aircraft measurements indicated fewer isolated SO2 plumes observed in summers, a 40 decrease of column SO2, and a 20 decrease of atmospheric optical depth (AOD) over Maryland after the implementation of local regulations on sulfur emissions from power plants (90 reduction from 2010). Surface observations of SO2 and particulate matter (PM) concentrations in Maryland show similar trends. OMI SO2 and MODIS AOD observations were used to investigate the column contents of air pollutants over the eastern U.S.; these indicate decreasing trends in column SO2 (60 decrease) and AOD (20 decrease). The decrease of upwind SO2 emissions also reduced aerosol loadings over the downwind Atlantic Ocean near the coast by 20, while indiscernible changes of the SO2 column were observed. A step change of SO2 emissions in Maryland starting in 20092010 had an immediate and profound benefit in terms of local surface SO2 concentrations but a modest impact on aerosol pollution, indicating that short-lived pollutants are effectively controlled locally, while long-lived pollutants require regional measures.

  19. Comparison and evaluation of anthropogenic emissions of SO2 and NOx over China

    Science.gov (United States)

    Li, Meng; Klimont, Zbigniew; Zhang, Qiang; Martin, Randall V.; Zheng, Bo; Heyes, Chris; Cofala, Janusz; Zhang, Yuxuan; He, Kebin

    2018-03-01

    Bottom-up emission inventories provide primary understanding of sources of air pollution and essential input of chemical transport models. Focusing on SO2 and NOx, we conducted a comprehensive evaluation of two widely used anthropogenic emission inventories over China, ECLIPSE and MIX, to explore the potential sources of uncertainties and find clues to improve emission inventories. We first compared the activity rates and emission factors used in two inventories and investigated the reasons of differences and the impacts on emission estimates. We found that SO2 emission estimates are consistent between two inventories (with 1 % differences), while NOx emissions in ECLIPSE's estimates are 16 % lower than those of MIX. The FGD (flue-gas desulfurization) device penetration rate and removal efficiency, LNB (low-NOx burner) application rate and abatement efficiency in power plants, emission factors of industrial boilers and various vehicle types, and vehicle fleet need further verification. Diesel consumptions are quite uncertain in current inventories. Discrepancies at the sectorial and provincial levels are much higher than those of the national total. We then examined the impacts of different inventories on model performance by using the nested GEOS-Chem model. We finally derived top-down emissions by using the retrieved columns from the Ozone Monitoring Instrument (OMI) compared with the bottom-up estimates. High correlations were observed for SO2 between model results and OMI columns. For NOx, negative biases in bottom-up gridded emission inventories (-21 % for MIX, -39 % for ECLIPSE) were found compared to the satellite-based emissions. The emission trends from 2005 to 2010 estimated by two inventories were both consistent with satellite observations. The inventories appear to be fit for evaluation of the policies at an aggregated or national level; more work is needed in specific areas in order to improve the accuracy and robustness of outcomes at finer spatial

  20. Intercomparison of Metop-A SO2 measure- ments during the 2010- 2011 Icelandic eruptions

    Directory of Open Access Journals (Sweden)

    Maria Elissavet Koukouli

    2015-03-01

    Full Text Available The European Space Agency project Satellite Monitoring of Ash and Sulphur Dioxide for the mitigation of Avi­ ation Hazards, was introduced after the eruption of the Icelandic volcano Eyjafjallajökull in the spring of 2010 to facilitate the development of an optimal End­to­End System for Volcanic Ash Plume Monitoring and Predic­ tion. The Eyjafjallajökull plume drifted towards Europe and caused major disruptions of European air traffic for several weeks affecting the everyday life of millions of people. The limitations in volcanic plume monitoring and prediction capabilities gave birth to this observational system which is based on comprehensive satellite­derived ash plume and sulphur dioxide [SO2] level estimates, as well as a widespread validation using supplementary satellite, aircraft and ground­based measurements. Inter­comparison of the volcanic total SO2 column and plume height observed by GOME­2/Metop­A and IASI/Metop­A are shown before, during and after the Eyjaf­ jallajökull 2010 eruptions as well as for the 2011 Grímsvötn eruption. Co­located ground­based Brewer Spectro­ photometer data extracted from the World Ozone and Ultraviolet Radiation Data Centre for de Bilt, the Nether­ lands, are also compared to the different satellite estimates. Promising agreement is found for the two different types of instrument for the SO2 columns with linear regression coefficients ranging around from 0.64 when comparing the different instruments and 0.85 when comparing the two different IASI algorithms. The agree­ ment for the plume height is lower, possibly due to the major differences between the height retrieval part of the GOME2 and IASI algorithms. The comparisons with the Brewer ground­based station in de Bilt, The Nether­ lands show good qualitative agreement for the peak of the event however stronger eruptive signals are required for a longer quantitative comparison. 

  1. Comparison and evaluation of anthropogenic emissions of SO2 and NOx over China

    Directory of Open Access Journals (Sweden)

    M. Li

    2018-03-01

    Full Text Available Bottom-up emission inventories provide primary understanding of sources of air pollution and essential input of chemical transport models. Focusing on SO2 and NOx, we conducted a comprehensive evaluation of two widely used anthropogenic emission inventories over China, ECLIPSE and MIX, to explore the potential sources of uncertainties and find clues to improve emission inventories. We first compared the activity rates and emission factors used in two inventories and investigated the reasons of differences and the impacts on emission estimates. We found that SO2 emission estimates are consistent between two inventories (with 1 % differences, while NOx emissions in ECLIPSE's estimates are 16 % lower than those of MIX. The FGD (flue-gas desulfurization device penetration rate and removal efficiency, LNB (low-NOx burner application rate and abatement efficiency in power plants, emission factors of industrial boilers and various vehicle types, and vehicle fleet need further verification. Diesel consumptions are quite uncertain in current inventories. Discrepancies at the sectorial and provincial levels are much higher than those of the national total. We then examined the impacts of different inventories on model performance by using the nested GEOS-Chem model. We finally derived top-down emissions by using the retrieved columns from the Ozone Monitoring Instrument (OMI compared with the bottom-up estimates. High correlations were observed for SO2 between model results and OMI columns. For NOx, negative biases in bottom-up gridded emission inventories (−21 % for MIX, −39 % for ECLIPSE were found compared to the satellite-based emissions. The emission trends from 2005 to 2010 estimated by two inventories were both consistent with satellite observations. The inventories appear to be fit for evaluation of the policies at an aggregated or national level; more work is needed in specific areas in order to improve the accuracy and robustness of

  2. Aqueous-phase mechanism for secondary organic aerosol formation from isoprene: application to the southeast United States and co-benefit of SO2 emission controls

    Directory of Open Access Journals (Sweden)

    E. A. Marais

    2016-02-01

    Full Text Available Isoprene emitted by vegetation is an important precursor of secondary organic aerosol (SOA, but the mechanism and yields are uncertain. Aerosol is prevailingly aqueous under the humid conditions typical of isoprene-emitting regions. Here we develop an aqueous-phase mechanism for isoprene SOA formation coupled to a detailed gas-phase isoprene oxidation scheme. The mechanism is based on aerosol reactive uptake coefficients (γ for water-soluble isoprene oxidation products, including sensitivity to aerosol acidity and nucleophile concentrations. We apply this mechanism to simulation of aircraft (SEAC4RS and ground-based (SOAS observations over the southeast US in summer 2013 using the GEOS-Chem chemical transport model. Emissions of nitrogen oxides (NOx  ≡  NO + NO2 over the southeast US are such that the peroxy radicals produced from isoprene oxidation (ISOPO2 react significantly with both NO (high-NOx pathway and HO2 (low-NOx pathway, leading to different suites of isoprene SOA precursors. We find a mean SOA mass yield of 3.3 % from isoprene oxidation, consistent with the observed relationship of total fine organic aerosol (OA and formaldehyde (a product of isoprene oxidation. Isoprene SOA production is mainly contributed by two immediate gas-phase precursors, isoprene epoxydiols (IEPOX, 58 % of isoprene SOA from the low-NOx pathway and glyoxal (28 % from both low- and high-NOx pathways. This speciation is consistent with observations of IEPOX SOA from SOAS and SEAC4RS. Observations show a strong relationship between IEPOX SOA and sulfate aerosol that we explain as due to the effect of sulfate on aerosol acidity and volume. Isoprene SOA concentrations increase as NOx emissions decrease (favoring the low-NOx pathway for isoprene oxidation, but decrease more strongly as SO2 emissions decrease (due to the effect of sulfate on aerosol acidity and volume. The US Environmental Protection Agency (EPA projects 2013–2025 decreases in

  3. Research progress of SO2 removal from flue gas by functionalized ionic liquids

    Directory of Open Access Journals (Sweden)

    Xinle SHI

    2017-02-01

    Full Text Available Functionalized ionic liquids are receiving increasing attention in the field of flue gas desulfurization due to its unique physical and chemical properties. Research progress on the field of SO2 removal by ionic liquids (ILs including guanidinium-based, amines-based and ether-based ILs is summarized. Industrial application of polymerization ILs and loaded ILs to desulfurization is reviewed. Relevant suggestions on industrial application of ionic liquids based on fundamental research are put forward. The first thing is to develop functional ionic liquid for desulfurization,and thus investigate and propose its desulfurization mechanism and model; the second is to carry out the research work on immobilized ionic liquid, and explore its recycling properties, thus prolonging its service life.

  4. Recent advances in ground-based ultraviolet remote sensing of volcanic SO2 fluxes

    Directory of Open Access Journals (Sweden)

    Euripides P. Kantzas

    2011-06-01

    Full Text Available Measurements of volcanic SO2 emission rates have been the mainstay of remote-sensing volcanic gas geochemistry for almost four decades, and they have contributed significantly to our understanding of volcanic systems and their impact upon the atmosphere. The last ten years have brought step-change improvements in the instrumentation applied to these observations, which began with the application of miniature ultraviolet spectrometers that were deployed in scanning and traverse configurations, with differential optical absorption spectroscopy evaluation routines. This study catalogs the more recent empirical developments, including: ultraviolet cameras; wide-angle field-of-view differential optical absorption spectroscopy systems; advances in scanning operations, including tomography; and improved understanding of errors, in particular concerning radiative transfer. Furthermore, the outcomes of field deployments of sensors during the last decade are documented, with respect to improving our understanding of volcanic dynamics and degassing into the atmosphere.

  5. Efficient capture of SO2 by a binary mixture of caprolactam tetrabutyl ammonium bromide ionic liquid and water.

    Science.gov (United States)

    Duan, Erhong; Guo, Bin; Zhang, Miaomiao; Guan, Yanan; Sun, Hua; Han, Jing

    2011-10-30

    The solubility of SO(2) in a binary mixture of water and caprolactam tetrabutyl ammonium bromide ionic liquid (CPL-TBAB IL) was investigated. Though the ionic liquid and water were fully miscible, a phase separation occurred when SO(2) was introduced into the mixture. The SO(2) concentrated in the lower layer, and it could be released by heating the solution under reduced pressure (382.2K, 10.1 kPa). After desorption, the mixture could be reused to absorb SO(2). It was found that SO(2) acts as a switch to cause the water and CPL-TBAB IL to phase separate, and the mechanics of this phase separation process was studied by gas chromatography-mass spectrometry, fourier transform-infrared spectroscopy and Karl-Fisher titration. The absorption and desorption of SO(2) in the CPL-TBAB/water mixtures were reversible. Copyright © 2011 Elsevier B.V. All rights reserved.

  6. NO and H2O2 contribute to SO2 toxicity via Ca2+ signaling in Vicia faba guard cells.

    Science.gov (United States)

    Yi, Min; Bai, Heli; Xue, Meizhao; Yi, Huilan

    2017-04-01

    NO and H 2 O 2 have been implicated as important signals in biotic and abiotic stress responses of plants to the environment. Previously, we have shown that SO 2 exposure increased the levels of NO and H 2 O 2 in plant cells. We hypothesize that, as signaling molecules, NO and H 2 O 2 mediate SO 2 -caused toxicity. In this paper, we show that SO 2 hydrates caused guard cell death in a concentration-dependent manner in the concentration range of 0.25 to 6 mmol L -1 , which was associated with elevation of intracellular NO, H 2 O 2 , and Ca 2+ levels in Vicia faba guard cells. NO donor SNP enhanced SO 2 toxicity, while NO scavenger c-PTIO and NO synthesis inhibitors L-NAME and tungstate significantly prevented SO 2 toxicity. ROS scavenger ascorbic acid (AsA) and catalase (CAT), Ca 2+ chelating agent EGTA, and Ca 2+ channel inhibitor LaCl 3 also markedly blocked SO 2 toxicity. In addition, both c-PTIO and AsA could completely block SO 2 -induced elevation of intracellular Ca 2+ level. Moreover, c-PTIO efficiently blocked SO 2 -induced H 2 O 2 elevation, and AsA significantly blocked SO 2 -induced NO elevation. These results indicate that extra NO and H 2 O 2 are produced and accumulated in SO 2 -treated guard cells, which further activate Ca 2+ signaling to mediate SO 2 toxicity. Our findings suggest that both NO and H 2 O 2 contribute to SO 2 toxicity via Ca 2+ signaling.

  7. Numerical simulation of flue gas purification from NOx, SO2 by electron beam

    International Nuclear Information System (INIS)

    Morgunov, V.V.; Shkilko, A.M.; Fainchtein, O.L.

    2011-01-01

    received: NO - 99.97%, NO 2 - -17.53% (the concentration growth was observed), SO 2 - 77.32% (without taking into consideration direct reaction SO 2 and NH 3 ); amount of selected species - 111; amount of selected reactions - 941. Elaborated computer code can be used for optimization of the EB flue gases purification technology, modeling kinetic mechanism of radiation-chemical processes in the flue gases, carry out numerical experiments.

  8. Smog chamber study on aging of combustion soot in isoprene/SO2/NOx system: Changes of mass, size, effective density, morphology and mixing state

    Science.gov (United States)

    Li, Kangwei; Chen, Linghong; Han, Ke; Lv, Biao; Bao, Kaiji; Wu, Xuecheng; Gao, Xiang; Cen, Kefa

    2017-02-01

    Atmospheric soot aging process is always accompanied by secondary particle formation, which is a comprehensive environmental issue that deserves great attention. On one hand, aging of primary soot could change its own physicochemical properties; on the other hand, complex air pollution caused by pollutant emission from various sources (e.g., vehicle exhausts, coal-fired flue gases and biogenic VOCs emission) may contribute to secondary particle formation onto primary particle surface. In this study, aging of combustion soot in isoprene/SO2/NOx system was investigated under controlled laboratory conditions in several smog chamber experiments. During the evolution of soot, several physical properties such as mass, size, effective density, morphology and mixing state were determined simultaneously by an integrated aerosol analytical system of Scanning Mobility Particle Sizer (SMPS), Differential Mobility Analyzer-Aerosol Particle Mass Analyzer-Condensation Particle Counter (DMA-APM-CPC) and Transmission Electron Microscopy coupled with Energy-dispersive X-ray Spectrometry (TEM/EDX) techniques. Here, based on the experimental results of soot aging under different gas-phase composition and relative humidity (RH), we firstly proposed possible aging pathways of soot in isoprene/SO2/NOx system. A synergetic effect was speculated to exist between SO2 and isoprene on soot aging process, which led to more secondary particle formation. At the same time, TEM/EDX analysis showed that a competitive mechanism between H2SO4(g) and isoprene oxidation vapor may exist: H2SO4(g) firstly condensed onto fresh soot, then an acceleration of isoprene oxidation products formed onto H2SO4 pre-coated soot. In isoprene/SO2/NOx system, high RH conditions could contribute to soot aging and new particle formation. The changes of effective density and dynamic shape factor of soot also indicated that high RH conditions could accelerate soot aging process, and led chain-like soot into more spherical

  9. A kinetic sensitivity analysis for the SO2 and NOx removal using the electron beam technology

    Science.gov (United States)

    Zwolińska, Ewa; Gogulancea, Valentina; Sun, Yongxia; Lavric, Vasile; Chmielewski, Andrzej

    2017-09-01

    The mathematical modeling of the phenomena taking place during the electron beam flue gas treatment is a complex endeavor due to the different time scales of the processes occurring as accelerated electrons are bombarding the flue gas. The paper presents a complex kinetic model for these gas phase interactions, consisting of 1034 chemical reactions with the participation of 115 reactive species. The mathematical model couples the complex gas phase kinetics with a liquid phase kinetic model, taking into account the nucleation and condensation phenomena occurring due to the presence of sulfuric acid. The modeling results for both coupled and uncoupled gas phase kinetics are validated against a set of literature experimental data with satisfactory outcome. The work aims to identify the most important chemical reactions influencing the pollutants removal, proposing a sensitivity analysis using the concept of generated entropy. To the best of the authors' knowledge a sensitivity analysis of this extent has not been performed for the electron beam flue gas treatment. The results of this analysis emphasize the link between the removal efficiencies of NOx and SO2, the importance of hydroxyl radicals and can aid in future model reduction efforts.

  10. Anthropogenic SO2/NOx committee summary of current status--annual inventory

    International Nuclear Information System (INIS)

    Benkovitz, C.M.

    1992-06-01

    At the First GEIA Workshop on Global Emissions Inventories, held in Baltimore, MD on December 1--2, 1991, data on anthropogenic emissions of sulfur and nitrogen developed by Dignon (1992) were selected to form the basis for the GEIA SO 2 and NO x annual inventories. The Dignon data include emissions from fuel combustion only and currently extend to 1980. The methodology used was detailed in Dignon and Hameed (1985) and consists of statistical regression models based on available emissions data from the U.S and some other member countries of the Organization of Economic Cooperation and Development (OECD), which includes Australia, Canada, Japan and western European countries. Control regulations are incorporated via the use of different statistical parameter The grid definition from these inventories was also adopted for the GEIA grid: origin at 180 degree W, 90 degree S, 1 degree x 1 degree resolution (i.e., 360 cells in the longitude direction, 180 cells in the latitude direction). To upgrade the basic GEIA inventories, data for the different geographic regions being solicited from researchers located within these areas. This paper contains the upgrades which have been accomplished to date

  11. Can China’s Industrial SO2 Emissions Trading Pilot Scheme Reduce Pollution Abatement Costs?

    Directory of Open Access Journals (Sweden)

    Zhengge Tu

    2014-10-01

    Full Text Available This paper evaluates the effects of China’s industrial SO2 emissions trading pilot scheme (SETPS on the pollution abatement costs (PAC from the past and future perspective. We apply the kernel-based propensity score difference-in-difference method to examine the effects of SETPS on the average pollution abatement costs (APAC and the marginal pollution abatement costs (MPAC based on the environment data from the industrial sector of 29 provinces in China over the period of 1998 to 2011. Our findings are that SETPS failed to reduce PAC as a whole. During 2002 to 2011, SETPS increased APAC by 1310 RMB per ton on average and had an insignificant negative effect on MPAC. Nevertheless, the conclusions would be markedly different if we separately investigated the effects of SETPS each year of the pilot period. The positive effects of SETPS on PAC started to appear since 2009, and SETPS significantly reduced both APAC and MPAC, especially in 2009 and 2011.

  12. Emission spectrum and relaxation kinetics of SO2 induced by 266 nm laser.

    Science.gov (United States)

    Zhang, Guiyin; Zhang, Lianshui; Jin, Yidong

    2010-09-15

    Laser induced fluorescence (LIF) emission spectrum of SO(2) in the range of 270.0-470.0 nm has been obtained with the quadruple harmonic output (266 nm) of a pulsed Nd:YAG laser as excitation source. The spectrum is composed of a continuous envelope in the short wavelength side, while it shows the character of banded structure superimposed on a continuous one in the long wavelength region. Fluorescence emission from the hybrid states of A(1)A(2)+B(1)B(1) and X(1)A(1)+B(1)B(1) forms the continuous envelope and phosphorescence emission from the triplet state a(3)B(1) forms the banded progression. It is also found that direct emission from laser excited states is very weak. The primary portion of the emission is from the energy levels populated by collision relaxation or collision induced intersystem crossing process. The harmonic frequencies and inharmonic coefficients of the symmetric stretching vibration and the bending vibration of X(1)A(1) state are derived from the ascription of the phosphorescence progression. Copyright 2010 Elsevier B.V. All rights reserved.

  13. Waterberg coal characteristics and SO2 minimum emissions standards in South African power plants.

    Science.gov (United States)

    Makgato, Stanford S; Chirwa, Evans M Nkhalambayausi

    2017-10-01

    Key characteristics of coal samples from the supply stock to the newly commissioned South African National Power Utility's (Eskom's) Medupi Power Station - which receives its supply coal from the Waterberg coalfield in Lephalale (Limpopo Province, South Africa) - were evaluated. Conventional coal characterisation such as proximate and ultimate analysis as well as determination of sulphur forms in coal samples were carried out following the ASTM and ISO standards. Coal was classified as medium sulphur coal when the sulphur content was detected in the range 1.15-1.49 wt.% with pyritic sulphur (≥0.51 wt.%) and organic sulphur (≥0.49 wt.%) accounted for the bulk of the total sulphur in coal. Maceral analyses of coal showed that vitrinite was the dominant maceral (up to 51.8 vol.%), whereas inertinite, liptinite, reactive semifusinite and visible minerals occurred in proportions of 22.6 vol.%, 2.9 vol.%, 5.3 vol.% and 17.5 vol.%, respectively. Theoretical calculations were developed and used to predict the resultant SO 2 emissions from the combustion of the Waterberg coal in a typical power plant. The sulphur content requirements to comply with the minimum emissions standards of 3500 mg/Nm 3 and 500 mg/Nm 3 were found to be ≤1.37 wt.% and ≤0.20 wt.%, respectively. Copyright © 2017 Elsevier Ltd. All rights reserved.

  14. Dry deposition of O3 and SO2 estimated from gradient measurements above a temperate mixed forest.

    Science.gov (United States)

    Wu, Zhiyong; Staebler, Ralf; Vet, Robert; Zhang, Leiming

    2016-03-01

    Vertical profiles of O3 and SO2 concentrations were monitored at the Borden Forest site in southern Ontario, Canada from May 2008 to April 2013. A modified gradient method (MGM) was applied to estimate O3 and SO2 dry deposition fluxes using concentration gradients between a level above and a level below the canopy top. The calculated five-year mean (median) dry deposition velocity (Vd) were 0.35 (0.27) and 0.59 (0.54) cm s(-1), respectively, for O3 and SO2. Vd(O3) exhibited large seasonal variations with the highest monthly mean of 0.68 cm s(-1) in August and the lowest of 0.09 cm s(-1) in February. In contrast, seasonal variations of Vd(SO2) were smaller with monthly means ranging from 0.48 (May) to 0.81 cm s(-1) (December). The different seasonal variations between O3 and SO2 were caused by the enhanced SO2 uptake by snow surfaces in winter. Diurnal variations showed a peak value of Vd in early morning in summer months for both O3 and SO2. Canopy wetness increased the non-stomatal uptake of O3 while decreasing the stomatal uptake. This also applied to SO2, but additional factors such as surface acidity also played an important role on the overall uptake. Crown Copyright © 2015. Published by Elsevier Ltd. All rights reserved.

  15. 40 CFR 53.32 - Test procedures for methods for SO2, CO, O3, and NO2.

    Science.gov (United States)

    2010-07-01

    ..., O3, and NO2. 53.32 Section 53.32 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... for SO2, CO, O3, and NO2. (a) Comparability. Comparability is shown for SO2, CO, O3, and NO2 methods... twenty-four (24) sequential 1-hour measurements. (6) For O3 and CO, no more than six 1-hour measurements...

  16. Highly Accurate Semi-Empirical IR Line Lists of Asymmetric SO2 Isotopologues: SO18O and SO17O

    Science.gov (United States)

    Huang, X.; Schwenke, D.; Lee, T. J.

    2015-12-01

    Atmosphere models and simulations of Venus, Mars, and Exo-planets will greatly benefit from complete and accurate Infrared spectra data of important molecules such as SO2 and CO2. Currently, high resolution spectra data for SO2 is very limited at 296K and mainly for the primary isotopologue 626. It cannot effectively support the observed data analysis and simulations. Recently we published a semi-empirically refined potential energy surface, denoted Ames-1, and Ames-296K IR line lists for SO2 626 and a few symmetric isotopologues including 646, 636, 666 and 828. The accuracy of line positions is around 0.01 - 0.03 cm-1 for most transitions. For intensities, most deviations are less than 5-15%. Now we have carried out new potential energy surface refinements by including latest experimental data and those of isotopologues. On the newly fitted surface, for the first time we have computed 296K line lists for the two most abundant asymmetric isotopologues, SO2 628 and SO2 627. We will present the spectra simulations of SO2 628 and SO2 627, and compare it with latest high resolution experimental spectroscopy of SO2 628. A composite "natural" line list at 296K is also available with terrestial abundances. These line lists will be available to download at http://huang.seti.org.

  17. Mechanistic Aspects of the Reversible Binding of SO2 on Arylplatinum Complexes: Experimental and ab Initio Studies

    NARCIS (Netherlands)

    Koten, G. van; Albrecht, M.A.; Gossage, R.A.; Frey, H.; Ehlers, A.W.; Baerends, E.J.; Merbach, A.E.

    2001-01-01

    The detailed mechanism of the reversible binding and fast exchange of SO2 on the organoplatinum(II) complex [PtI(NCN)], 1, has been studied experimentally in solution (C2F4Br2) using low-temperature NMR spectroscopy and theoretically by ab initio calculations. Direct bonding of SO2 and formation of

  18. PHYSIOLOGICAL-EFFECTS OF LONG-TERM EXPOSURE TO LOW CONCENTRATIONS OF SO2 AND NH3 ON POPLAR LEAVES

    NARCIS (Netherlands)

    VANHOVE, LWA; VANKOOTEN, O; VANWIJK, KJ; VREDENBERG, WJ; ADEMA, EH; PIETERS, GA

    Shoots of poplar (Populus euramericana L. cv. Flevo) were exposed to filtered air, SO2, NH3 or a mixture of SO2 and NH3 for 7 weeks in fumigation chambers. After this exposure gas exchange measurements were carried out using a leaf chamber. As compared to leaves exposed to filtered air, leaves

  19. Volcanic SO2 fluxes derived from satellite data: a survey using OMI, GOME-2, IASI and MODIS

    Directory of Open Access Journals (Sweden)

    N. Theys

    2013-06-01

    Full Text Available Sulphur dioxide (SO2 fluxes of active degassing volcanoes are routinely measured with ground-based equipment to characterize and monitor volcanic activity. SO2 of unmonitored volcanoes or from explosive volcanic eruptions, can be measured with satellites. However, remote-sensing methods based on absorption spectroscopy generally provide integrated amounts of already dispersed plumes of SO2 and satellite derived flux estimates are rarely reported. Here we review a number of different techniques to derive volcanic SO2 fluxes using satellite measurements of plumes of SO2 and investigate the temporal evolution of the total emissions of SO2 for three very different volcanic events in 2011: Puyehue-Cordón Caulle (Chile, Nyamulagira (DR Congo and Nabro (Eritrea. High spectral resolution satellite instruments operating both in the ultraviolet-visible (OMI/Aura and GOME-2/MetOp-A and thermal infrared (IASI/MetOp-A spectral ranges, and multispectral satellite instruments operating in the thermal infrared (MODIS/Terra-Aqua are used. We show that satellite data can provide fluxes with a sampling of a day or less (few hours in the best case. Generally the flux results from the different methods are consistent, and we discuss the advantages and weaknesses of each technique. Although the primary objective of this study is the calculation of SO2 fluxes, it also enables us to assess the consistency of the SO2 products from the different sensors used.

  20. Non-isothermal effects on SO2 absorption by water droplets. I - Model development. II - Results and discussion

    Science.gov (United States)

    Reda, M.; Carmichael, G. R.

    1982-01-01

    An analytic model of SO2 absorption in a falling water droplet is developed and a simulation of SO2 washout is performed. Nonisothermic effects on drop growth, droplet physical parameters, reaction rates, and multicomponent diffusion are treated in the model. The gas-liquid interface is assumed to be at equilibrium, and interfacial resistance is negligible. Raindrops are simulated as falling from a 2 km height through an atmospheric region containing SO2. The droplets decrease in size from evaporation and cooling, and their slightly basic pH aids SO2 absorption. The simulation indicates higher SO2 absorption at higher altitudes, and desorption may occur at ground level. Isothermal effects are concluded to be significant, and quantification of effects will depend on further modelling.

  1. An analysis of SO2 emission compliance under the 1990 Clean Air Act Amendments

    International Nuclear Information System (INIS)

    Hanson, D.A.; Cilek, C.M.; Pandola, G.; Taxon, T.

    1992-01-01

    The effectiveness of SO 2 emission allowance trading under Title 4 of the 1990 Amendments to the Clean Air Act (CAA) is of great interest due to the innovative nature of this market incentive approach. However, it may be a mistake to frame the compliance problem for a utility as a decision to trade or not. Trading of allowances should be the consequence, not the decision. The two meaningful decision variables for a utility are the control approaches chosen for its units and the amount of allowances to hold in its portfolio of assets for the future. The number allowances to be bought or sold (i.e. traded) is determined by the emission reduction and banking decisions. Our preferred approach is to think of the problem in terms of ABC's of the 1990 CAA Amendments: abatement strategy, banking, and cost competitiveness. The implications of the general principles presented in this paper on least cost emission reductions and emissions banking to hedge against risk are being simulated with version 2 of the ARGUS model representing the electric utility sector and regional coal supplies and transportation rates. A rational expectations forecast for allowances prices is being computed. The computed allowance price path has the property that demand for allowances by electric utilities for current use or for banking must equal the supply of allowances issued by the federal government or provided as forward market contracts in private market transactions involving non-utility speculators. From this rational expectations equilibrium forecast, uncertainties are being explored using sensitivity tests. Some of the key issues are the amount of scrubbing and when it is economical to install it, the amount of coal switching and how much low sulfur coal premiums will be bid up; and the amount of emission trading within utilities and among different utilities

  2. Formation of secondary aerosols from the ozonolysis of styrene: Effect of SO2 and H2O

    Science.gov (United States)

    Díaz-de-Mera, Yolanda; Aranda, Alfonso; Martínez, Ernesto; Rodríguez, Ana Angustias; Rodríguez, Diana; Rodríguez, Ana

    2017-12-01

    In this work we report the study of the ozonolysis of styrene and the reaction conditions leading to the formation of secondary aerosols. The reactions have been carried out in a Teflon chamber filled with synthetic air mixtures at atmospheric pressure and room temperature. We have found that the ozonolysis of styrene in the presence of low concentrations of SO2 readily produces new particles under concentrations of reactants lower than those required in experiments in the absence of SO2. Thus, nucleation events occur at concentrations around (5.6 ± 1.7) × 108molecule cm-3 (errors are 2σ±20%) and SO2 is consumed during the experiments. The reaction of the Criegee intermediates with SO2 to produce SO3 and then H2SO4 may explain (together with OH reactions' contribution) the high capacity of styrene to produce particulate matter in polluted atmospheres. The formation of secondary aerosols in the smog chamber is inhibited under high H2O concentrations. So, the potential formation of secondary aerosols under atmospheric conditions depends on the concentration of SO2 and relative humidity, with a water to SO2 rate constants ratio kH2O/kSO2 = (2.8 ± 0.7) × 10-5 (errors are 2σ±20%).

  3. Optimization of CO2 Absorption Characteristic under the Influence of SO2 in Flue Gas by Hollow Fiber Membrane Contactor

    Directory of Open Access Journals (Sweden)

    Ziyi Qu

    2016-01-01

    Full Text Available Hollow fiber membrane contactor is a new, highly efficient, and the most promising technology for CO2 absorption in flue gas. There is still SO2 that exists in the flue gas after desulfurization tower of power plant. This paper studied the influence of SO2 on CO2 absorption characteristic in flue gas by hollow fiber membrane contactor with absorbent of EDA, EDA + MEA (0.6 : 0.4, and EDA + MEA + PZ (0.4 : 0.4 : 0.2. The influences of SO2 concentration, cycle absorption and desorption characteristic of absorbent, absorbent concentration, and liquid-gas flow rate ratio are studied to analyze the influence of SO2 on CO2 absorption characteristic. The appropriate absorbent composition ratio and appropriate parameter range that can inhibit the influence of SO2 are proposed by studying the hybrid sorbent with activating agent, appropriate absorbent concentration, and ratio of liquid-gas flow rate. Among the three kinds of absorbents, EDA + MEA + PZ (0.4 : 0.4 : 0.2 had the best tolerance ability to SO2 and the highest efficiency. With comprehensive consideration of CO2 removal efficiency and operating cost, under the condition of 1000 ppm SO2, the appropriate concentration and liquid-gas flow rate ratio of EDA, EDA + MEA, and EDA + MEA + PZ are proposed.

  4. Infrared Spectra of Novel NgBeSO2 Complexes (Ng = Ne, Ar, Kr, Xe) in Low Temperature Matrixes.

    Science.gov (United States)

    Yu, Wenjie; Liu, Xing; Xu, Bing; Xing, Xiaopeng; Wang, Xuefeng

    2016-11-03

    The novel noble-gas complexes NgBeSO 2 (Ng = Ne, Ar, Kr, Xe) have been prepared in the laser-evaporated beryllium atom reactions with SO 2 in low-temperature matrixes. Doped with heavier noble gas, the guest (Ar, Kr, Xe) atom can substitute neon to form more stable complex. Infrared spectroscopy and theoretical calculations are used to confirm the band assignment. The dissociation energies are calculated at 0.9, 4.0, 4.7, and 6.0 kcal/mol for NeBeSO 2 , ArBeSO 2 , KrBeSO 2 , and XeBeSO 2 , respectively, at the CCSD(T) level. Quantum chemical calculations demonstrate that the Ng-Be bonds in NgBeSO 2 could be formed by the combination of electron-donation and ion-induced dipole interactions. The Wiberg bond index (WBI) values of Ng-Be bonds and LOL (localized orbital locator) profile indicate that the Ng-Be bond exhibits a gradual increase in covalent character along Ne to Xe.

  5. TOMS/N7 MS SO2 Vertical Column 1-Orbit L2 Swath 50x50 km V2.00 (TOMSN7SO2) at GES DISC

    Data.gov (United States)

    National Aeronautics and Space Administration — The goal of this data set is to create and archive a Level 2 SO2 Earth Science Data Record (ESDR) from backscatter Ultraviolet (BUV) measurements from Total Ozone...

  6. Multi-source SO2 emission retrievals and consistency of satellite and surface measurements with reported emissions

    Directory of Open Access Journals (Sweden)

    V. Fioletov

    2017-10-01

    Full Text Available Reported sulfur dioxide (SO2 emissions from US and Canadian sources have declined dramatically since the 1990s as a result of emission control measures. Observations from the Ozone Monitoring Instrument (OMI on NASA's Aura satellite and ground-based in situ measurements are examined to verify whether the observed changes from SO2 abundance measurements are quantitatively consistent with the reported changes in emissions. To make this connection, a new method to link SO2 emissions and satellite SO2 measurements was developed. The method is based on fitting satellite SO2 vertical column densities (VCDs to a set of functions of OMI pixel coordinates and wind speeds, where each function represents a statistical model of a plume from a single point source. The concept is first demonstrated using sources in North America and then applied to Europe. The correlation coefficient between OMI-measured VCDs (with a local bias removed and SO2 VCDs derived here using reported emissions for 1° by 1° gridded data is 0.91 and the best-fit line has a slope near unity, confirming a very good agreement between observed SO2 VCDs and reported emissions. Having demonstrated their consistency, seasonal and annual mean SO2 VCD distributions are calculated, based on reported point-source emissions for the period 1980–2015, as would have been seen by OMI. This consistency is further substantiated as the emission-derived VCDs also show a high correlation with annual mean SO2 surface concentrations at 50 regional monitoring stations.

  7. Removal of SO2 and NO/sub x/ from flue gas by means of a spray dryer/electron beam combination: a feasibility study

    International Nuclear Information System (INIS)

    Helfritch, D.J.; Feldman, P.L.; Ray, A.B.; Morgan, J.R.; Hildreth, G.A.

    1982-04-01

    This study examines the feasibility of adding an electron beam between the spray dryer and the fabric filter of dry scrubber flue gas desulfurization (FGD) systems. The beam promises effective removal of nitrogen oxides (NO/sub x/) and sulfur dioxide (SO 2 ), even at higher coal-sulfur levels than usually economic for dry scrubbers. The beam excites gas molecules, promoting reactions that convert SO 2 and NO/sub x/ to acids that then react with calcium compounds and are removed by the filter. Concerns examined here are feasibility and waste disposal. The cost findings are promising for both manufacture and operation. The system uses commercially available components. The relatively low temperatures and high humidity downstream of the spray dryer favor economic beam operation. The beam removes SO 2 , so the dryer can be run for economy, not high removal. The beam's incidental heating effect reduces reheat cost. Safe landfilling of the nitrate-rich waste appears practical, with leachate carrying no more nitrate than natural rain and dustfall. We expect natural pozzolanic reactions between alumina-silica compounds in the fly ash and lime compounds from the spray dryer to form an impermeable concrete-like material within 10 days after landfilling. Dry scrubber with electron beam appears competitive with commercial FGD systems, and we recommend a pilot scale operation

  8. Effect of SO2 on the performance of Ag-Pd/Al2O3 for the selective catalytic reduction of NOx with C2H5OH.

    Science.gov (United States)

    Xie, Shu-xia; Yu, Yun-bo; Wang, Jin; He, Hong

    2006-01-01

    The influence of SO2 on the performance of Ag-Pd/Al2O3 for the selective catalytic reduction (SCR) of NOx with C2H5OH was investigated experimentally. The activity test results suggest that Ag-Pd/Al203 shows a small activity loss in the presence of SO2 when using C2H5OH as a reductant. In situ DRIFTS spectra show that the activity loss originates from the formation of surface sulphate species on the Ag-Pd/Al2O3. The surface sulphate species formation inhibits the formation of nitrate, whereas hardly changes the partial oxidation of C2HsOH. Compared with the NOx reduction by C3H6 an obvious suppression of the surface sulphate species formation was observed by DRIFTS experiment when using C2H50H as a reductant. This phenomenon reveals the better catalytic performance and strong SO2 tolerance of Ag-Pd/Al2O3-C2H5OH system.

  9. Validating the accuracy of SO2 gas retrievals in the thermal infrared (8-14 μm)

    Science.gov (United States)

    Gabrieli, Andrea; Porter, John N.; Wright, Robert; Lucey, Paul G.

    2017-11-01

    Quantifying sulfur dioxide (SO2) in volcanic plumes is important for eruption predictions and public health. Ground-based remote sensing of spectral radiance of plumes contains information on the path-concentration of SO2. However, reliable inversion algorithms are needed to convert plume spectral radiance measurements into SO2 path-concentrations. Various techniques have been used for this purpose. Recent approaches have employed thermal infrared (TIR) imaging between 8 μm and 14 μm to provide two-dimensional mapping of plume SO2 path-concentration, using what might be described as "dual-view" techniques. In this case, the radiance (or its surrogate brightness temperature) is computed for portions of the image that correspond to the plume and compared with spectral radiance obtained for adjacent regions of the image that do not (i.e., "clear sky"). In this way, the contribution that the plume makes to the measured radiance can be isolated from the background atmospheric contribution, this residual signal being converted to an estimate of gas path-concentration via radiative transfer modeling. These dual-view approaches suffer from several issues, mainly the assumption of clear sky background conditions. At this time, the various inversion algorithms remain poorly validated. This paper makes two contributions. Firstly, it validates the aforementioned dual-view approaches, using hyperspectral TIR imaging data. Secondly, it introduces a new method to derive SO2 path-concentrations, which allows for single point SO2 path-concentration retrievals, suitable for hyperspectral imaging with clear or cloudy background conditions. The SO2 amenable lookup table algorithm (SO2-ALTA) uses the MODTRAN5 radiative transfer model to compute radiance for a variety (millions) of plume and atmospheric conditions. Rather than searching this lookup table to find the best fit for each measured spectrum, the lookup table was used to train a partial least square regression (PLSR) model

  10. Measurement of sulfur dioxide oxidation rates in wintertime orographic clouds

    International Nuclear Information System (INIS)

    Snider, J.R.

    1990-01-01

    SO2-reaction studies in the clouds are examined and summarized to experimentally confirm model predictions and previous field studies regarding dominant SO2-reaction pathways. Controlled amounts of SO2 were released into nonprecipitating orographic clouds, and sulfate yields are compared to oxidant depletions. The sulfate yields were taken from cloud-water samples and liquid-water-concentration measurements, and oxidant-depletion data were generated from continuous gas-phase measurements. Comparisons of Y sub SO4 and D sub H2O2 suggest that H2O2 is the dominant oxidant, and the in-cloud reaction between H2O2 and the bisulfite ion can be expressed by a simple rate that agrees with predictions and laboratory results. The rate measurements are found to be inconsistent with the rate law proposed by Hegg and Hobbs (1982) and with some observational data. The present conclusions are of interest to evaluating the effects of sulfur dioxide emissions on sulfuric acid deposition. 30 refs

  11. Long-term trends in airborne SO2in an air quality monitoring station in Seoul, Korea, from 1987 to 2013.

    Science.gov (United States)

    Khan, Azmatullah; Kim, Ki-Hyun; Szulejko, Jan E; Brown, Richard J C; Jeon, Eui-Chan; Oh, Jong-Min; Shin, Yong Soon; Adelodun, Adedeji A

    2017-08-01

    Atmospheric concentration of sulfur dioxide (SO 2 ) was intermittently measured at an air quality monitoring (AQM) station in the Yong-san district of Seoul, Korea, between 1987 and 2013. The SO 2 level was compared with other important pollutants concurrently measured, including methane (CH 4 ), carbon monoxide (CO), nitric oxide (NO), nitrogen dioxide (NO 2 ), ozone (O 3 ), and particulate matter (PM 10 ). If split into three different periods (period 1, 1987-1988, period 2, 1999-2000, and period 3, 2004-2013), the respective mean [SO 2 ] values (6.57 ± 4.29, 6.30 ± 2.44, and 5.29 ± 0.63 ppb) showed a slight reduction across the entire study period. The concentrations of SO 2 are found to be strongly correlated with other pollutants such as CO (r = 0.614, p = 0.02), which tracked reductions in reported emissions due to tighter emissions standards enacted by the South Korean government. There was also a clear seasonal trend in the SO 2 level, especially in periods 2 and 3, reflecting the combined effects of domestic heating by coal briquettes and meteorological conditions. Although only a 16% concentration reduction was achieved during the 27-year study duration, this is significant if one considers rapid urbanization, an 83.2% increase in population, and rapid industrialization that took place during that period. Since 1970, a network of air quality monitoring (AQM) stations has been operated by the Korean Ministry of Environment (KMOE) for routine nationwide monitoring of air pollutant concentrations in urban/suburban areas. To date, the information obtained from these stations has provided a platform for analyzing long-term trends of major pollutant species. In this study, we examined the long-term trends of SO 2 levels and relevant environmental parameters monitored continuously in the Yong-san district of Seoul between 1987 and 2013. The data were analyzed over various time scales (i.e., monthly, seasonal, and annual intervals). The results obtained from

  12. The effect of coal-fired power-plant SO2 and NOx control technologies on aerosol nucleation in the source plumes

    Directory of Open Access Journals (Sweden)

    E. M. Knipping

    2012-12-01

    Full Text Available Nucleation in coal-fired power-plant plumes can greatly contribute to particle number concentrations near source regions. The changing emissions rates of SO2 and NOx due to pollution-control technologies over recent decades may have had a significant effect on aerosol formation and growth in the plumes with ultimate implications for climate and human health. We use the System for Atmospheric Modeling (SAM large-eddy simulation model with the TwO-Moment Aerosol Sectional (TOMAS microphysics algorithm to model the nucleation in plumes of coal-fired plants. We test a range of cases with varying emissions to simulate the implementation of emissions-control technologies between 1997 and 2010. We start by simulating the W. A. Parish power plant (near Houston, TX during this time period, when NOx emissions were reduced by ~90% and SO2 emissions decreased by ~30%. Increases in plume OH (due to the reduced NOx produced enhanced SO2 oxidation and an order-of-magnitude increase in particle nucleation in the plume despite the reduction in SO2 emissions. These results suggest that NOx emissions could strongly regulate particle nucleation and growth in power-plant plumes. Next, we test a range of cases with varying emissions to simulate the implementation of SO2 and NOx emissions-control technologies. Particle formation generally increases with SO2 emission, while NOx shows two different regimes: increasing particle formation with increasing NOx under low-NOx emissions and decreasing particle formation with increasing NOx under high-NOx emissions. Next, we compare model results with airborne measurements made in the W. A. Parish power-plant plume in 2000 and 2006, confirming the importance of NOx emissions on new particle formation and highlighting the substantial effect of background aerosol loadings on this process (the more polluted background of the 2006 case caused more than an order-of-magnitude reduction in particle formation in the plume compared to

  13. Smog chamber studies on the air chemistry of biogenic hydrocarbons in the presence of ozone, NOx and SO2

    International Nuclear Information System (INIS)

    Nolting, F.; Zetzsch, C.

    1990-01-01

    The influence of SO 2 on the photochemical degradation processes of the biogenic hydrocarbon α-pinene was studied with respect to the present forest decline. For that purpose premixed air was irradiated with simulated sunlight in laboratory experiments using a modified smog chamber. The performance of a novel semi continuous analyzer for H 2 SO 4 /sulfate was tested for smog chamber studies of the transformation of SO 2 to sulfuric acid and sulfur containing aerosol. An influence of SO 2 on the formation of ozone was not detected. The rates of degradation cannot be described by gas phase reactions alone, and, in addition, they are faster in the presence of humidity. Depending on humidity, 30-50% of the consumed SO 2 can be recovered in the suspended aerosol. In the presence of 60% relative humidity the nearly exclusive product is sulfur aerosol that needs further characterization. (orig.) With 9 figs., 42 refs [de

  14. Continuing global monitoring of anthropogenic and volcanic SO2 sources from Aura/OMI to SNPP/OMPS

    Science.gov (United States)

    Li, C.; Krotkov, N. A.; Carn, S. A.; Joiner, J.; McLinden, C. A.; Fioletov, V.

    2017-12-01

    Sulfur dioxide (SO2) is an important trace gas that has significant impacts on air quality, the climate, and stratospheric ozone. It is predominantly emitted from anthropogenic sources such as coal-fired power plants and smelters, but also has sizable sources from volcanic activity. The Ozone Monitoring Instrument (OMI) aboard NASA's Earth Observing System (EOS) Aura spacecraft has been providing global observations of both anthropogenic and volcanic SO2 since its launch in 2004. The Ozone Mapping and Profiler Suite (OMPS) nadir mapper, launched aboard the NASA/NOAA Suomi National Polar-orbiting Partnership (SNPP) satellite in 2011, will continue the 13+ year OMI SO2 time series. However, it is a significant challenge to build a coherent data record between OMI and OMPS, as the SO2 signal is relatively weak and its retrieval is subject to a number of interferences such as ozone absorption. Additionally, the two instruments also have different spectral and spatial resolutions that result in different sensitivities to SO2. Even a relatively small error in retrievals, due to either algorithmic or instrumental factors, may lead to a large inter-instrument bias in SO2. In this presentation, we report on our latest effort and progress in developing EOS continuity SNPP/OMPS SO2 products. We have applied a consistent retrieval technique based on principal component analysis (PCA) of measured radiance data to both OMI and OMPS. We show that the PCA retrieval technique, which extracts principal components (PCs) from measured radiances and applies these PCs in spectral fitting to minimize the effects of various interfering processes, is capable of producing highly consistent OMI and OMPS SO2 data for both anthropogenic sources and large volcanic eruptions. To gain a quantitative understanding of the two instruments' capabilities of monitoring SO2 sources, we have also applied a new emission estimation technique that combines satellite SO2 and wind information to both of them

  15. Integrated Dry NOx/SO2 Emissions Control System, A DOE Assessment

    Energy Technology Data Exchange (ETDEWEB)

    National Energy Technology Laboratory

    2001-10-01

    The goal of the U.S. Department of Energy's (DOE) Clean Coal Technology (CCT) Program is to furnish the energy marketplace with a number of advanced, more efficient, and environmentally responsible coal utilization technologies through demonstration projects. These projects seek to establish the commercial feasibility of the most promising advanced coal technologies that have developed beyond the proof-of-concept stage. This document serves as a DOE post-project assessment (PPA) of a project selected in CCT Round III, the Integrated Dry NO{sub x}/SO{sub 2} Emissions Control System (IDECS), as described in a Report to Congress (U.S. Department of Energy 1991). The desire to reduce emissions of nitrogen oxides (NO, nitric oxide, and NO{sub 2}, nitrogen dioxide, collectively referred to as NO{sub x}) and sulfur dioxide (SO{sub 2}) by up to 70 percent at a minimum capital expenditure, while limiting waste production to dry solids that can be handled by conventional ash-removal equipment, prompted Public Service Company of Colorado (PSCC) to submit the proposal for the IDECS project. In March 1991, PSCC entered into a cooperative agreement with DOE to conduct the study. The project was sited at PSCC's Arapahoe Steam Electric Generating Station in Denver, Colorado. The purpose of this CCT project was to demonstrate the reduction of NO{sub x} and SO{sub 2} emissions by installing a combination of existing and emerging technologies, which were expected to work synergistically to reduce emissions. The technologies were low-NO{sub x} burners (LNBS), overfire air (OFA), and selective noncatalytic reduction (SNCR) for NO{sub x} reduction; and dry sorbent injection (DSI), both with and without flue-gas humidification (FGH), for SO{sub 2} reduction. DOE provided 50 percent of the total project funding of $26.2 million.

  16. Study on the Removal of SO2 from Simulated Flue Gas Using Dry Calcium-Spray with DBD Plasma

    International Nuclear Information System (INIS)

    Yi Chengwu; Wu Chundu; Chen Zhigang; Ou Hongxiang; Shao Xuejun

    2008-01-01

    In this study, lime-hydrate (Ca(OH) 2 ) desulfurizer was treated by plasma with strong ionization discharge of a dielectric barrier. The removal of SO 2 from simulated flue gas was investigated. The principles of SO 2 removal are discussed. Several factors affecting the efficiency of SO 2 removal were studied. They included the ratio of calcium to sulfur (Ca/S), desulfurizer granularity, residence time of the flue gas, voltage applied to the discharge electrode in the plasma generator, and energy consumption. Experimental results indicate that the increase in Ca/S ratio, the applied voltage and discharge power, the residence time, and the reduction in the desulfurizer granularity all can raise the SO 2 removal efficiency. The SO 2 removal efficiency was up to 91.3% under the following conditions, namely a primary concentration of SO2 of 2262 x 10 -6 (v/v) in the emission gas, 21%(v/v) of oxygen, 1.8% (v/v) of water, a Ca/S ratio of 1.48, a residence time of 2.8 s, a 3.4 kV voltage and a 10 kHz frequency power applied to the discharge electrodes in the plasma generator, and a flow rate of 100 m 3 /h for emission gas.

  17. Volcanic SO2 by UV-TIR satellite retrievals: validation by using ground-based network at Mt. Etna

    Directory of Open Access Journals (Sweden)

    Claudia Spinetti

    2015-03-01

    Full Text Available Mt. Etna volcano in Italy is one of the most active degassing volcanoes worldwide, emitting a mean of 1.7 Mt/year of Sulphur Dioxide (SO2 in quiescent periods. In this work, SO2 measurements retrieved by Moderate Resolution Imaging Spectroradiometer (MODIS, hyper-spectral Infrared Atmospheric Sounding Interferometer (IASI and the second Global Ozone Monitoring Experiment (GOME-2 data are compared with the ground-based data from the FLux Automatic MEasurement monitoring network (FLAME. Among the eighteen lava fountain episodes occurring at Mt. Etna in 2011, the 10 April paroxysmal event has been selected as a case-study for the simultaneous observation of the SO2 cloud by satellite and ground-based sensors. For each data-set two retrieval techniques were adopted and the measurements of SO2 mass and flux with their respective uncertainty were obtained. With respect to the FLAME SO2 mass of 4.5 Gg, MODIS, IASI and GOME-2 differ by about 10%, 15% and 30%, respectively. The SO2 flux correlation coefficient between MODIS and FLAME is 0.84. All the retrievals within the respective errors are in agreement with the ground-based measurements supporting the validity of these space measurements. 

  18. SO2 EMISSION MEASUREMENT BY DOAS (DIFFERENTIAL OPTICAL ABSORPTION SPECTROSCOPY AND COSPEC (CORRELATION SPECTROSCOPY AT MERAPI VOLCANO (INDONESIA

    Directory of Open Access Journals (Sweden)

    Hanik Humaida

    2010-06-01

    Full Text Available The SO2 is one of the volcanic gases that can use as indicator of volcano activity. Commonly, SO2 emission is measured by COSPEC (Correlation Spectroscopy. This equipment has several disadvantages; such as heavy, big in size, difficulty in finding spare part, and expensive. DOAS (Differential Optical Absorption Spectroscopy is a new method for SO2 emission measurement that has advantages compares to the COSPEC. Recently, this method has been developed. The SO2 gas emission measurement of Gunung Merapi by DOAS has been carried out at Kaliadem, and also by COSPEC method as comparation. The differences of the measurement result of both methods are not significant. However, the differences of minimum and maximum result of DOAS method are smaller than that of the COSPEC. It has range between 51 ton/day and 87 ton/day for DOAS and 87 ton/day and 201 ton/day for COSPEC. The measurement of SO2 gas emission evaluated with the seismicity data especially the rockfall showed the presence of the positive correlation. It may cause the gas pressure in the subsurface influencing instability of 2006 eruption lava.   Keywords: SO2 gas, Merapi, DOAS, COSPEC

  19. First Observations of SO2 from the Satellite Suomi NPP OMPS: Widespread Air Pollution Events Over China

    Science.gov (United States)

    Yang, Kai; Dickerson, Russell R.; Carn, Simon A.; Ge, Cui; Wang, Jun

    2013-01-01

    Severe smog episodes over China in January 2013 received worldwide attention. This air pollution was distinguished by heavy loadings of fine particulate matter and SO2. To characterize these episodes, we employed the Ozone Mapping and Profiler Suite, Nadir Mapper (OMPS NM), an ultraviolet (UV) spectrometer flying on the Suomi National Polar-orbiting Partnership (SNPP) spacecraft since October 2011. We developed an advanced algorithm to quantify SO2 in the lower troposphere and achieved high-quality retrievals from OMPS NM, which are characterized by high precision, approx. 0.2 Dobson Units (DU; 1 DU = 2.69 x 10(exp 16) molecules/sq cm) for instantaneous field of view SO2 data and low biases (within +/-0.2 DU). Here we report SO2 retrievals and UV aerosol index data for these pollution events. The SO2 columns and the areas covered by high pollutant concentrations are quantified; the results reveal for the first time the full extent (an area of approx. 10(exp 6) sq km containing up to 60 kt of SO2) of these episodes.

  20. Improvement of SO2 removal by the solubility change of Ca(OH)2 in the spray dryer system.

    Science.gov (United States)

    Song, H C; Park, J W

    2001-09-01

    Experiments were carried out to verify the effect of the solubility change of the Ca(OH)2 sorbent on the removal of SO2 in a lab-scale spray dryer system. First, to identify the solubility effect, HNO3 was added into Ca(OH)2 slurry to increase the solubility of Ca(OH)2 by neutralization. The improvement of SO2 removal by 5-10% occurred under the condition of both 50% relative solubility and constant pH of slurry. But SO2 removal efficiency decreased steeply when the relative solubility approached 100% and the pH of the slurry decreased rapidly. For the practical application of the solubility effect, NH4Cl and NH4OH were selected as additives. Ammonium chloride (NH4Cl) which could improved Ca(OH)2 solubility removed more SO2 by 5-10% than NH4OH which showed no change in solubility. The optimal result was obtained when the slurry was fed at the ratio of 0.25mol NH4Cl/mol Ca(OH)2. The Ca(OH),/NH4Cl sorbent could remove more SO2 and improve Ca(OH)2 utilization than Ca(OH)2 sorbent in the Ca/S stoichiometric range of 1.0-1.4. It was concluded that the increase of sorbent solubility made the improvement in SO2 removal efficiency and Ca(OH)2 utilization.

  1. A two-photon fluorescent turn-on probe for imaging of SO2 derivatives in living cells and tissues

    International Nuclear Information System (INIS)

    Zhu, Xiaoyan; Zhu, Longming; Liu, Hong-wen; Hu, Xiaoxiao; Peng, Rui-zi; Zhang, Jing; Zhang, Xiao-Bing; Tan, Weihong

    2016-01-01

    SO 2 and its derivatives (bisulfite/sulfite) play crucial roles in several physiological processes. Therefore, development of reliable analytical methods for monitoring SO 2 and its derivatives in biological systems is very significant. In this paper, a FRET-based two-photon fluorescent turn-on probe, A-HCy, was proposed for specific detection of SO 2 derivatives through the bisulfite/sulfite-promoted Michael addition reaction. In this FRET system, an acedan (2-acetyl-6-dialkylaminonaphthalene) moiety was selected as a two-photon donor and a hemicyanine derivative served as both the quencher and the recognition unit for bisulfite/sulfite. A-HCy exhibited excellent selectivity and rapid response to HSO 3 − with a detection limit of 0.24 μM. More importantly, probe A-HCy was first successfully applied in two-photon fluorescence imaging of biological SO 2 derivatives in living cells and tissues, suggesting its great potential for practical application in biological systems. - Highlights: • A FRET-based two-photon fluorescent probe for detecting SO 2 derivatives was proposed. • The probe shows high sensitivity, excellent selectivity, rapid response as well as low cytotoxicity. • The probe was capable of detecting SO 2 derivatives up to 170 μm depth in tissues.

  2. In-situ functionalization of mesoporous hexagonal ZnO synthesized in task specific ionic liquid as a photocatalyst for elimination of SO2, NOx, and CO

    Science.gov (United States)

    Kowsari, Elaheh; Abdpour, Soheil

    2017-12-01

    A novel mesoporous structure of zinc oxide was synthesized in hydrothermal autocalve in the presence of a functional ionic liquid (FIL) {[CH2CH2] O2 (mm)2}. This FIL with ether groups was used simultaneously as a designer templating agent and a source of the hydroxyl radical. The presence of this ionic liquid led to producing ethylene glycol in the reaction media, which adsorb on the surface of mesoporous hexagonal ZnO plates. These mesoporous structures can adsorb pollutant gases and increase photocatalytic oxidation of pollutant gases in compare with commercial ZnO nanoparticles and agglomerated nanoparticles synthesized in this work. XPS data confirmed ethylene glycol production by the ionic liquid, which could prove a role for ionic liquids as designers. The estimated BET surface area values of ZnO hexagonal mesoporous plates and agglomerated particles were 84 m2/g and 12 m2/g respectively. Optical properties of the mesoporous structures were analyzed by photoluminescence spectroscopy and diffuse reflectance UV-visible spectroscopy. The performance of these structures as efficient photocatalysts was further demonstrated by their removal of NOx, SO2, and CO under UV irradiation. The removal of NOx, SO2, and CO under UV irradiation was 56%, 81%, and 35% respectively, after 40 min of irradiation time. Reusability of the photocatalyst was determined; the results show no significant decrease of activity of photocatalyst. after five cycles.

  3. Detailed Information Security in Cloud Computing

    OpenAIRE

    Pavel Valerievich Ivonin

    2013-01-01

    The object of research in this article is technology of public clouds, structure and security system of clouds. Problems of information security in clouds are considered, elements of security system in public clouds are described.

  4. Increases to Biogenic Secondary Organic Aerosols from SO2 and NOx in the Southeastern US

    Science.gov (United States)

    Russell, L. M.; Liu, J.; Ruggeri, G.; Takahama, S.; Claflin, M. S.; Ziemann, P. J.; Lee, A.; Murphy, B.; Pye, H. O. T.; Ng, N. L.; McKinney, K. A.; Surratt, J. D.

    2017-12-01

    During the 2013 Southern Oxidant and Aerosol Study, Fourier Transform Infrared Spectroscopy (FTIR) and Aerosol Mass Spectrometer (AMS) measurements of submicron mass were collected at Look Rock, Tennessee, and Centreville, Alabama. The low NOx, low wind, little rain, and increased daytime isoprene emissions led to multi-day stagnation events at Look Rock that provided clear evidence of particle-phase sulfate enhancing biogenic secondary organic aerosol (bSOA) by selective uptake. Organic mass (OM) sources were apportioned as 42% "vehicle-related" and 54% bSOA, with the latter including "sulfate-related bSOA" that correlated to sulfate (r=0.72) and "nitrate-related bSOA" that correlated to nitrate (r=0.65). Single-particle mass spectra showed three composition types that corresponded to the mass-based factors with spectra cosine similarity of 0.93 and time series correlations of r>0.4. The vehicle-related OM with m/z 44 was correlated to black carbon, "sulfate-related bSOA" was on particles with high sulfate, and "nitrate-related bSOA" was on all particles. The similarity of the m/z spectra (cosine similarity=0.97) and the time series correlation (r=0.80) of the "sulfate-related bSOA" to the sulfate-containing single-particle type provide evidence for particle composition contributing to selective uptake of isoprene oxidation products onto particles that contain sulfate from power plants. Since Look Rock had much less NOx than Centreville, comparing the bSOA at the two sites provides an evaluation of the role of NOx for bSOA. CO and submicron sulfate and OM concentrations were 15-60 % higher at Centreville than at Look Rock but their time series had moderate correlations of r= 0.51, 0.54, and 0.47, respectively. However, NOx had no correlation (r=0.08) between the two sites. OM correlated with the higher NOx levels at Centreville but with O3 at Look Rock. OM sources identified by Positive Matrix Factorization had three very similar factors at both sites from FTIR

  5. Synergetic formation of secondary inorganic and organic aerosol: effect of SO2 and NH3 on particle formation and growth

    Directory of Open Access Journals (Sweden)

    B. Chu

    2016-11-01

    Full Text Available The effects of SO2 and NH3 on secondary organic aerosol formation have rarely been investigated together, while the interactive effects between inorganic and organic species under highly complex pollution conditions remain uncertain. Here we studied the effects of SO2 and NH3 on secondary aerosol formation in the photooxidation system of toluene∕NOx in the presence or absence of Al2O3 seed aerosols in a 2 m3 smog chamber. The presence of SO2 increased new particle formation and particle growth significantly, regardless of whether NH3 was present. Sulfate, organic aerosol, nitrate, and ammonium were all found to increase linearly with increasing SO2 concentrations. The increases in these four species were more obvious under NH3-rich conditions, and the generation of nitrate, ammonium, and organic aerosol increased more significantly than sulfate with respect to SO2 concentration, while sulfate was the most sensitive species under NH3-poor conditions. The synergistic effects between SO2 and NH3 in the heterogeneous process contributed greatly to secondary aerosol formation. Specifically, the generation of NH4NO3 was found to be highly dependent on the surface area concentration of suspended particles, and increased most significantly with SO2 concentration among the four species under NH3-rich conditions. Meanwhile, the absorbed NH3 might provide a liquid surface layer for the absorption and subsequent reaction of SO2 and organic products and, therefore, enhance sulfate and secondary organic aerosol (SOA formation. This effect mainly occurred in the heterogeneous process and resulted in a significantly higher growth rate of seed aerosols compared to without NH3. By applying positive matrix factorisation (PMF analysis to the AMS data, two factors were identified for the generated SOA. One factor, assigned to less-oxidised organic aerosol and some oligomers, increased with increasing SO2 under NH3-poor conditions, mainly due to the well

  6. Synergetic formation of secondary inorganic and organic aerosol: effect of SO2 and NH3 on particle formation and growth

    Science.gov (United States)

    Chu, Biwu; Zhang, Xiao; Liu, Yongchun; He, Hong; Sun, Yele; Jiang, Jingkun; Li, Junhua; Hao, Jiming

    2016-11-01

    The effects of SO2 and NH3 on secondary organic aerosol formation have rarely been investigated together, while the interactive effects between inorganic and organic species under highly complex pollution conditions remain uncertain. Here we studied the effects of SO2 and NH3 on secondary aerosol formation in the photooxidation system of toluene/NOx in the presence or absence of Al2O3 seed aerosols in a 2 m3 smog chamber. The presence of SO2 increased new particle formation and particle growth significantly, regardless of whether NH3 was present. Sulfate, organic aerosol, nitrate, and ammonium were all found to increase linearly with increasing SO2 concentrations. The increases in these four species were more obvious under NH3-rich conditions, and the generation of nitrate, ammonium, and organic aerosol increased more significantly than sulfate with respect to SO2 concentration, while sulfate was the most sensitive species under NH3-poor conditions. The synergistic effects between SO2 and NH3 in the heterogeneous process contributed greatly to secondary aerosol formation. Specifically, the generation of NH4NO3 was found to be highly dependent on the surface area concentration of suspended particles, and increased most significantly with SO2 concentration among the four species under NH3-rich conditions. Meanwhile, the absorbed NH3 might provide a liquid surface layer for the absorption and subsequent reaction of SO2 and organic products and, therefore, enhance sulfate and secondary organic aerosol (SOA) formation. This effect mainly occurred in the heterogeneous process and resulted in a significantly higher growth rate of seed aerosols compared to without NH3. By applying positive matrix factorisation (PMF) analysis to the AMS data, two factors were identified for the generated SOA. One factor, assigned to less-oxidised organic aerosol and some oligomers, increased with increasing SO2 under NH3-poor conditions, mainly due to the well-known acid catalytic effect of

  7. [Characterizing spatial patterns of NO(x), SO2 and O3 in Pearl River Delta by passive sampling].

    Science.gov (United States)

    Zhao, Yang; Shao, Min; Wang, Chen; Wang, Bo-Guang; Lu, Si-Hua; Zhong, Liu-Ju

    2011-02-01

    Concentrations of NO(x), SO2 and O3 were measured by passive sampling within 200km x 200km grid in Pearl River Delta (PRD). Sampling period was two weeks in November, 2009. Spatial distributions of NO(x), SO2 and O3 were obtained by Kriging interpolation method. The results were compared with emission inventories and modeling results. The transportations of O3 were evaluated by using backward trajectories of air parcels. During the sampling period, the mean concentrations of NO(x), SO2 and O3 were 75.9 microg/m3, 37.3 microg/m3 and 36.2 microg/m3, respectively. And the highest concentrations of NO(x), SO2 and O3 were 195.7 microg/m3, 95.9 microg/m3 and 81.8 microg/m3. Comparing with routine measurements from the regional monitoring network in PRD, the results by passive method were 18.6%, 33.5% and 37.5% lower for NO(x), SO2 and O3, respectively. The spatial patterns demonstrated that higher NO(x) concentrations often appeared in cities such as Guangzhou, Foshan and Shenzhen. SO2 concentrations were higher in west and lower in east. High SO2 concentrations are mainly from emission of power plants and industrial sources. Concentrations of O3 showed the highest levels in the south of PRD. Backward trajectory analysis for higher ozone areas indicated that 53% of the air masses were from the region with high concentration of NO(x). The horizontal transportation caused higher ozone in the south while lower in north in PRD.

  8. VizieR Online Data Catalog: Collisional excitation of sulfur dioxide, SO2, in cold molecular c

    Science.gov (United States)

    Cernicharo, J.; Spielfiedel, A.; Balanca, C.; Dayou, F.; Senent, M.-L.; Feautrier, N.; Faure, A.; Cressiot-Vincent, L.; Wiesenfeld, L.; Pardo, J. R.

    We present collisional rate coefficients for SO2 with ortho an molecular hydrogen for the physical conditions prevailing in dark molecular clouds. Rate coefficients for the first 31 rotational levels of this species (energies up to 55K) and for temperatures between 5 and 30K are provided. We have found that these rate coefficients are about ten times more than those previously computed for SO2 with helium. We calculated the expected emission of the centimeter wavelength lines of SO2. We find that the transition connecting the metastable 202 level with the 111 one is in absorption against the cosmic background for a wide range of densities. The 404-313 line is found to be inverted for densities below a few 104cm-3. We observed the 111-202 transition with the 100m Green Bank Telescope towards some dark clouds. The line is observed, as expected, in absorption and provides an abundance of SO2 in these objects of a few 10-10^. The potential use of millimeter lines of SO2 as tracers of the physical conditions of dark clouds is discussed. (3 data files).

  9. A performance study of simultaneous microbial removal of no and SO2 in a biotrickling-filter under anaerobic condition

    Directory of Open Access Journals (Sweden)

    Yaqiong Han

    2011-06-01

    Full Text Available The behaviors of simultaneous removal of NO and SO2 using the coculture of anaerobic denitrifying bacteria and sulfate reducing bacteria was investigated in a bench-scale biotrickling-filter. When the combined NO/SO2 removal biotrickling-filter was operated at an empty bed residence time of 76 s with NO and SO2 feed concentrations of 2 and 2 g/m3, respectively, the SO2 removal efficiency was always above 95%, while NO removal exhibited an evident periodicity of 5-6 days for the initial 60 days after the attachment phase. A steady-state NO-removal efficiency of around 90% was obtained after 130 days of continuous operation. Experimental results indicated that the coculture in the combined NO/SO2 removal biotrickling-filter showed a higher resistance to shock NO-loadings and a better tolerance to starvation than the single denitrifying bacteria in the NO removal biotrickling-filter.

  10. Study of meteorological aspects and urban concentration of SO2 in atmospheric environment of La Plata, Argentina.

    Science.gov (United States)

    Ratto, Gustavo; Videla, Fabián; Almandos, J Reyna; Maronna, Ricardo; Schinca, Daniel

    2006-10-01

    This article presents and discusses SO(2) (ppbv) concentration measurements combined with meteorological data (mainly wind speed and direction) for a five-year campaign (1996 to 2000), in a site near an oil refinery plant close to the city of La Plata and surroundings (aprox. 740.000 inh.), considered one of the six most affected cities by air pollution in the country. Since there is no monitoring network in the area, the obtained results should be considered as medium term accumulated data that enables to determine trends by analyzing together gas concentrations and meteorological parameters. Preliminary characterization of the behaviour of the predominant winds of the region in relation with potential atmospheric gas pollutants from seasonal wind roses is possible to carry out from the data. These results are complemented with monthly averaged SO(2) measurements. In particular, for year 2000, pollutant roses were determined which enable predictions about contamination emission sources. As a general result we can state that there is a clear increase in annual SO(2) concentration and that the selected site should be considered as a key site for future survey monitoring network deployment. Annual SO(2) average concentration and prevailing seasonal winds determined in this work, together with the potential health impact of SO(2) reveals the need for a comprehensive and systematic study involving particulate matter an other basic pollutant gases.

  11. Volcanic Ash and SO2 retrievals using synthetic MODIS TIR data: comparison between inversion procedures and sensitivity analysis

    Directory of Open Access Journals (Sweden)

    Stefano Corradini

    2015-02-01

    Full Text Available In this work the volcanic ash and SO2 retrievals obtained by applying three different procedures (LUT - Look Up Table, NN - Neural Network and VPR - Volcanic Plume Removal on MODIS Thermal InfraRed (TIR synthetic measurements have been compared. The synthetic measurements are generated using MODTRAN Radiative Transfer Model (RTM for defined volcanic cloud configurations. The results, presented as the percentage difference between the retrieved ash and SO2 total masses and the true values used for the synthetic data generation, indicate maximum differences of +/- 15% and +/- 10% for all the procedures and for ash and SO2 retrievals respectively. A sensitivity analysis has been also realized to investigate the influence of volcanic cloud altitude and water vapour profile on SO2 retrievals at 7.3 and 8.6 μm. Results confirm the high sensitivity of the 7.3 μm retrieval to the volcanic cloud altitude and show that the SO2 total masses estimated at 7.3 and 8.6 μm separately can be used to improve the information on the plume height. Finally, the water vapour profile is used to compute the minimum altitude over which the 7.3 μm retrieval is effective. 

  12. CHARACTERIZATION TESTING AND ANALYSIS OF SINGLE CELL SO2 DEPOLARIZED ELECTROLYZER

    Energy Technology Data Exchange (ETDEWEB)

    Steimke, J; Timothy Steeper, T

    2006-09-15

    This document reports work performed at the Savannah River National Laboratory (SRNL) that further develops the use of a proton exchange membrane or PEM-type electrochemical cell to produce hydrogen via SO{sub 2}-depolarized water electrolysis. This work was begun at SRNL in 2005. This research is valuable in achieving the ultimate goal of an economical hydrogen production process based on the Hybrid Sulfur (HyS) Cycle. The HyS Process is a hybrid thermochemical cycle that may be used in conjunction with advanced nuclear reactors or centralized solar receivers to produce hydrogen by water-splitting. Like all other sulfur-based cycles, HyS utilizes the high temperature thermal decomposition of sulfuric acid to produce oxygen. The unique aspect of HyS is the generation of hydrogen in a water electrolyzer that is operated under conditions where dissolved sulfur dioxide depolarizes the anodic reaction, resulting in substantial voltage reduction. Sulfur dioxide is oxidized at the anode, producing sulfuric acid that is sent to the acid decomposition portion of the cycle. The focus of this work was to conduct single cell electrolyzer tests in order to prove the concept of SO{sub 2}-depolarization and to determine how the results can be used to evaluate the performance of key components of the HyS Process. A test facility for conducting SO{sub 2}-depolarized electrolyzer (SDE) testing was designed, constructed and commissioned. The maximum cell current is 50 amperes, which is equivalent to a hydrogen production rate of approximately 20 liters per hour. Feed to the anode of the electrolyzer is sulfuric acid solutions containing dissolved sulfur dioxide. The partial pressure of sulfur dioxide may be varied in the range of 1 to 6 atm (15 to 90 psia). Temperatures may be controlled in the range from ambient to 80 C. Hydrogen generated at the cathode of the cell is collected for the purpose of flow measurement and composition analysis. The test facility proved to be easy to

  13. Gaseous (DMS, MSA, SO2, H2SO4 and DMSO and particulate (sulfate and methanesulfonate sulfur species over the northeastern coast of Crete

    Directory of Open Access Journals (Sweden)

    H. Bardouki

    2003-01-01

    Full Text Available A detailed study of the levels, the temporal and diurnal variability of the main compounds involved in the biogenic sulfur cycle was carried out in Crete (Eastern Mediterranean during the Mediterranean Intensive Oxidant Study (MINOS field experiment in July-August 2001. Intensive measurements of gaseous dimethylsulfide (DMS, dimethylsulfoxide (DMSO, sulfur dioxide (SO2, sulfuric (H2SO4 and methanesulfonic acids (MSA and particulate sulfate (SO42- and methanesulfonate (MS- have been performed during the campaign. Dimethylsulfide (DMS levels ranged from 2.9 to 136 pmol·mol-1 (mean value of 21.7 pmol·mol-1 and showed a clear diurnal variation with daytime maximum. During nighttime DMS levels fall close or below the detection limit of 2 pmol·mol-1. Concurrent measurements of OH and NO3 radicals during the campaign indicate that NO3 levels can explain most of the observed diurnal variation of DMS. Dimethylsulfoxide (DMSO ranged between 0.02 and 10.1 pmol·mol-1 (mean value of 1.7 pmol·mol-1 and presents a diurnal variation similar to that of DMS. SO2 levels ranged from 220 to 2970 pmol·mol-1 (mean value of 1030 pmol·mol-1, while nss-SO42- and MS- ranged from 330 to 7100 pmol·mol-1, (mean value of 1440 pmol·mol-1 and 1.1 to 37.5 pmol·mol-1 (mean value of 11.5 pmol·mol-1 respectively. Of particular interest are the measurements of gaseous MSA and H2SO4. MSA ranged from below the detection limit (3x104 to 3.7x107 molecules cm-3, whereas H2SO4 ranged between 1x105 and 9.0x107 molecules cm-3. The measured H2SO4 maxima are among the highest reported in literature and can be attributed to high insolation, absence of precipitation and increased SO2 levels in the area. From the concurrent SO2, OH, and H2SO4 measurements a sticking coefficient of 0.52±0.28 was calculated for H2SO4. From the concurrent MSA, OH, and DMS measurements the yield of gaseous MSA from the OH-initiated oxidation of DMS was calculated to range between 0.1-0.4%. This low MSA

  14. Electric utility strategies for controlling SO2 under Title IV (acid deposition control) of the 1990 Clean Air Act Amendments

    International Nuclear Information System (INIS)

    Kinsman, J.D.; Evans, J.E.; Clendenin, J.H.

    1992-01-01

    The Clean Air Act Amendments of 1990 call for U.S. electric utility to further control emissions of SO 2 and NO x . This article describes Title IV requirements and the status of rulemaking; Title IV costs; uncertainties with SO 2 control decisions; state regulatory activities; and compliance options and actions to date. Some of the conclusions of the paper are: (1) a functioning SO 2 allowance trading market would allow great flexibility and a national solution approaching least-cost, but it is unclear whether the allowance market will be allowed to work in an unconstrained manner; (2) to date, the market has not developed due to uncertainties related to engineer/fuel issues and, more importantly, state and Federal regulatory activities (and inactivity); and (3) coal switching appears to be the compliance strategy of choice in Phase I, along with intracompany allowance transactions

  15. Experimental and mechanism research of SO(2) removal by cast iron scraps in a magnetically fixed bed.

    Science.gov (United States)

    Jiang, Ju-Hui; Li, Ya-Hong; Cai, Wei-Min

    2008-05-01

    Sulfur dioxide can be effectively removed by cast iron scraps corrosion process in a DC magnetically fixed bed, and iron sulfate compounds are gained as an available byproduct. At approximate 50 degrees C, when magnetic field intensity was at 15 mT and height of scraps was about 25 mm, the SO(2) removal efficiency can be kept above 80%. As the deposited rusts accumulated, the corrosion rate and desulfurization efficiency gradually decreased. The results show SO(2) removal efficiency depends on corrosion rate, and it can be obviously enhanced by DC magnetic field. With the XRD and SEM research, it can be found that DC magnetic field cannot change the crystal structure of rusts, but can make the surface morphologies on the surface of scraps looser which means easily to be removed. Consequently, the corrosion resistance can be lessened and SO(2) removal efficiency is improved significantly.

  16. Oorlewing van die skerpioen Opistophthalmus pugnax (Scorpionidae ná blootstelling aan ’n letale dosis SO2-gas

    Directory of Open Access Journals (Sweden)

    Willie J. van Aardt

    2013-02-01

    Full Text Available Skerpioene is bekend vir hul aanpasbaarheid by toestande in ’n droë habitat, min voedsel en radioaktiewe bestraling. Niks is bekend oor hul aanpasbaarheid by skadelike gasse nie. Resultate van hierdie eksperiment by Opistophthalmus pugnax bewys dat hulle ’n hoë dosis van 1000 dele per miljoen SO2 kan oorleef wat nie die geval is by die mens nie. Byvoorbeeld, die suurstofverbruikskoers neem eerder toe van 4.16 µmol/g-1 uur-1 na 7.69 µmol/g-1uur-1, een uur ná blootstelling aan SO2. Veertig minute na blootstelling was die ṀO2 steeds bykans twee keer hoër in vergelyking met die ṀO2 aan die begin. Hierdie bevinding moet deur verdere eksperimente nagevors word, veral wat die rol van spirakulumsluiting speel by blootstelling aan SO2.

  17. Profiling the SO2 Plume from Volcan Turrialba: Ticosonde Balloon Measurements Compared with OMI and OMPS Retrievals

    Science.gov (United States)

    Selkirk, Henry; Krotkov, Nickolay; Li, Can; Morris, Gary (Inventor); Diaz, Jorge Andres; Carn, Simon; Vomel, Holger; Corrales, Ernesto; Nord, Paul; Larson, Kelsey

    2014-01-01

    The summit of Volcan Turrialba (elev. 3340 m) lies less than 50 km upstream in the prevailing easterlies from the Ticosonde balloon launch site at San Jose, Costa Rica, where ECC ozone sondes have been launched regularly since 2005. In 2006 we began to see telltale notches in the ozone profiles in the altitude range between 2 and 6 km. Given the proximity of Turrialba, it seemed likely that SO2 in the volcano's plume was interfering in the chemical reaction in the ECC ozone sonde used to detect ozone. In early 2010, fumarolic activity in the Turrialba crater increased strongly, and the profile notches in our soundings increased in frequency as well, consistent with this hypothesis. In February 2012 we tested a dual ECC sonde system, where an additional sonde is flown on the same payload using a selective SO2 filter. The difference of the measurements in the dual sonde is a direct measure of the amount of SO2 encountered. This first dual sonde passed through the plume, and the data indicated a tropospheric SO2 column of 1.4 DU, comparing favorably with a total column of 1.7 DU in the OMI 3-km linear fit (LF) product at the sonde profile location and at nearly the same time. We are now launching dual sondes on a regular basis with 18 launches in the first 12 months through July 2014; 11 of these have detectable SO2 signals. These soundings have great potential for validation of the Aura OMI and the Suomi-NPP OMPS retrievals of SO2. Here we present the sonde measurements and compare them with two satellite datasets: the Aura OMI Linear Fit (LF) product and the Suomi-NPP OMPS Principal Components Analysis (PCA) boundary layer product. The PCA algorithm reduces retrieval noise and artifacts by more accurately accounting for various interferences in SO2 retrievals such as O3 absorption and rotational Raman scattering. The comparisons with the in situ observations indicate a significant improvement of the PCA algorithm in capturing relatively weak volcanic SO2 signals.

  18. Representations of the q-deformed algebras Uq (so2,1) and Uq (so3,1)

    International Nuclear Information System (INIS)

    Gavrilik, O.M.; Klimyk, A.U.

    1993-01-01

    Representations of algebra U q (so 2 ,1) are studied. This algebra is a q-deformation of the universal enveloping algebra U(so 2 ,1) of the Lie algebra of the group SO 0 (2,1) and differs from the quantum algebra U q (SU 1 ,1). Classifications of irreducible representations and of infinitesimally irreducible representations of U q (SU 1 ,1). The sets of irreducible representations and of infinitesimally unitary irreducible representations of the algebra U q (so 3 ,1) are given. We also consider representations of U q (so n ,1) which are of class 1 with respect to subalgebra U q (so n ). (author). 22 refs

  19. Characterization of the chemistry at the anode and cathode in the Li/SO2 battery system

    Science.gov (United States)

    Kilroy, W. P.; Anderson, C. R.

    1983-05-01

    The discharge product of Li/SO2 cells discharged at 25 C at 1-2 mA/sq cm was quantitatively analyzed for sulfite, thiosulfate, and dithionite. Analysis of the lithium anodes of commercial Li/SO2 batteries by XPS, SAM, SEM, and mass spectroscopy techniques determined the passive film chemistry to be complex, but generally dominated by lithium sulfite and sulfate formation. The anode micostructure and chemistry is inhomogeneous and sensitively dependent upon the state of discharge and the discharge temperature.

  20. Theoretical description of functionality, applications, and limitations of SO2 cameras for the remote sensing of volcanic plumes

    Directory of Open Access Journals (Sweden)

    U. Platt

    2010-06-01

    Full Text Available The SO2 camera is a novel device for the remote sensing of volcanic emissions using solar radiation scattered in the atmosphere as a light source for the measurements. The method is based on measuring the ultra-violet absorption of SO2 in a narrow wavelength window around 310 nm by employing a band-pass interference filter and a 2 dimensional UV-sensitive CCD detector. The effect of aerosol scattering can in part be compensated by additionally measuring the incident radiation around 325 nm, where the absorption of SO2 is about 30 times weaker, thus rendering the method applicable to optically thin plumes. For plumes with high aerosol optical densities, collocation of an additional moderate resolution spectrometer is desirable to enable a correction of radiative transfer effects. The ability to deliver spatially resolved images of volcanic SO2 distributions at a frame rate on the order of 1 Hz makes the SO2 camera a very promising technique for volcanic monitoring and for studying the dynamics of volcanic plumes in the atmosphere. This study gives a theoretical basis for the pertinent aspects of working with SO2 camera systems, including the measurement principle, instrument design, data evaluation and technical applicability. Several issues are identified that influence camera calibration and performance. For one, changes in the solar zenith angle lead to a variable light path length in the stratospheric ozone layer and therefore change the spectral distribution of scattered solar radiation incident at the Earth's surface. The varying spectral illumination causes a shift in the calibration of the SO2 camera's results. Secondly, the lack of spectral resolution inherent in the measurement technique leads to a non-linear relationship between measured weighted average optical density and the SO2 column density. Thirdly, as is the case with all remote sensing techniques that use scattered solar radiation as a light source, the radiative transfer

  1. Effect of SO2 concentration as an impurity on carbon steel corrosion under subcritical CO2 environment

    Science.gov (United States)

    Mahlobo, MGR; Premlall, K.; Olubambi, PA

    2017-12-01

    Carbon dioxide (CO2) is considered to be easier to transport over moderate distances when turned into supercritical state (dense phase) than at any other state. Because of this reason, the transportation of CO2 during carbon capture and storage requires CO2 to be at its supercritical state. CO2 temperature profile from different regions causes CO2 to deviate between supercritical and subcritical state (gas/liquid phase). In this study the influence of sulphur dioxide (SO2) on the corrosion of carbon steel was evaluated under different SO2 concentrations (0.5, 1.5 and 5%) in combination with subcritical CO2. Scanning Electron Microscopy (SEM), X-Ray Diffraction (XRD) and Energy-Dispersive X-ray Spectroscopy (EDS) were used to characterize the CO2 corrosion product layer formed on the carbon steel surface. The weight loss results showed that corrosion rate increased with SO2 concentration with corrosion rate up to 7.45 mm/year while at 0% SO2 the corrosion rate was 0.067 mm/year.

  2. Physicochemical effects of discrete CO2-SO2 mixtures on injection and storage in a sandstone aquifer

    NARCIS (Netherlands)

    Waldmann, S.; Hofstee, C.; Koenen, M.; Loeve, D.

    2016-01-01

    Geological storage of captured CO2, which typically will contain certain amounts of impurities, in salineaquifers is of potential to reduce greenhouse gas emissions into the atmosphere. The co-injection of theimpurity SO2has an effect on the chemical reactivity of the fluid and solid phases as well

  3. High-Power Short Pulsed Corona: Investigation of Electrical Parameters, Abatement of SO2 and Ozone Generation

    International Nuclear Information System (INIS)

    Pokryvailo, A.; Yankelevich, Y.

    2001-01-01

    Electrical performance and chemical activity of a 50 MW, 100 kV, 22ns pulsed corona was studied in simulated air-SO 2 gas mixture in a coaxial reactor. Infrared and mass spectrometers and electrochemical sensors were used for gas diagnostics; solid byproducts were identified using X-ray fluorescent spectrometry. Electrochemical methods of gas diagnostics were not sufficiently reliable in view of the cross-influence of different gases, especially in ozone presence. The removal efficiency of SO 2 decreased at lower pollutant concentration and higher frequency, while the pulse energy was kept invariant. Removal efficiency in dry mixture was 25 g/kWh; in humid air, it was several times greater, which is attributed to the influence of OH radicals. In dry SO 2 -air mixture, the removal efficiency was much higher at positive polarity. Traces of many compounds were found and identified in treated gas. The precipitation of a yellowish powder identified as sulfur was observed. This effect was not previously noted in literature. It is ascribed to direct breaking of atomic bonds of the SO 2 molecule by energetic species. PSpice-based engineering model of corona-generator system is proposed. It was found that preliminary simulation results are in fair agreement with experimental data. The simulation revealed that surprisingly small part of the energy is coupled to plasma

  4. A case study of Asian dust storm particles: chemical composition, reactivity to SO2 and hygroscopic properties.

    Science.gov (United States)

    Ma, Qingxin; Liu, Yongchun; Liu, Chang; Ma, Jinzhu; He, Hong

    2012-01-01

    Mineral dust comprises a great fraction of the global aerosol loading, but remains the largest uncertainty in predictions of the future climate due to its complexity in composition and physico-chemical properties. In this work, a case study characterizing Asian dust storm particles was conducted by multiple analysis methods, including SEM-EDS, XPS, FT-IR, BET, TPD/mass and Knudsen cell/mass. The morphology, elemental fraction, source distribution, true uptake coefficient for SO2, and hygroscopic behavior were studied. The major components of Asian dust storm particles are aluminosilicate, SiO2 and CaCO3, with organic compounds and inorganic nitrate coated on the surface. It has a low reactivity towards SO2 with a true uptake coefficient, 5.767 x 10(-6), which limits the conversion of SO2 to sulfate during dust storm periods. The low reactivity also means that the heterogeneous reactions of SO2 in both dry and humid air conditions have little effect on the hygroscopic behavior of the dust particles.

  5. An experimental study on effect of coke ratio on SO2 and NOx emissions in sintering process

    Science.gov (United States)

    Wang, Hui; Zhang, Pu; Yang, Jingling

    2018-02-01

    By using the sinter cup experiment, the effects of different coke ratios of 0%, 25%, 50%, 75%, and 100% on the formation and total emissions of SO2 and NOx in the sintering process were studied with the Testo350 flue gas analyzer. The experimental results show that the emissions of SO2 and NOx are closely related to sintering process. With the increase of the coke proportion, the sintering temperature changes and the maximum peak time appears earlier. SO2 concentration has a bimodal distribution and NOx concentration has a triple peak. Besides, the both maximum peaks appear at the end of sintering. In addition, due to the increasing of the S and N contents in the fuel with the coke ratios from 0% to 100%, the amounts of SO2 and NOx emissions are raised respectively at 10.82 mg, 11.42 mg, 13.84 mg, 13.69 mg, 20.36 mg and 3.11 mg, 3.39 mg, 4.44 mg, 4.31 mg, 6.16 mg.

  6. 78 FR 47191 - Air Quality Designations for the 2010 Sulfur Dioxide (SO2) Primary National Ambient Air Quality...

    Science.gov (United States)

    2013-08-05

    ... Fallon, Acting Unit Chief, Air Colorado, Montana, North Quality Planning Unit, EPA Region Dakota, South Dakota, Utah and VIII, 1595 Wynkoop Street, Denver, CO Wyoming. 80202-1129, (303) 312-6281. Doris Lo, Air... measures that reduce SO 2 can generally be expected to reduce people's exposures to all gaseous SO X . This...

  7. Using CATS Near-Real-time Lidar Observations to Monitor and Constrain Volcanic Sulfur Dioxide (SO2) Forecasts

    Science.gov (United States)

    Hughes, E. J.; Yorks, J.; Krotkov, N. A.; da Silva, A. M.; Mcgill, M.

    2016-01-01

    An eruption of Italian volcano Mount Etna on 3 December 2015 produced fast-moving sulfur dioxide (SO2) and sulfate aerosol clouds that traveled across Asia and the Pacific Ocean, reaching North America in just 5 days. The Ozone Profiler and Mapping Suite's Nadir Mapping UV spectrometer aboard the U.S. National Polar-orbiting Partnership satellite observed the horizontal transport of the SO2 cloud. Vertical profiles of the colocated volcanic sulfate aerosols were observed between 11.5 and 13.5 km by the new Cloud Aerosol Transport System (CATS) space-based lidar aboard the International Space Station. Backward trajectory analysis estimates the SO2 cloud altitude at 7-12 km. Eulerian model simulations of the SO2 cloud constrained by CATS measurements produced more accurate dispersion patterns compared to those initialized with the back trajectory height estimate. The near-real-time data processing capabilities of CATS are unique, and this work demonstrates the use of these observations to monitor and model volcanic clouds.

  8. Air Pollution Inequality and Its Sources in SO2 and NOX Emissions among Chinese Provinces from 2006 to 2015

    Directory of Open Access Journals (Sweden)

    Mohaddeseh Azimi

    2018-01-01

    Full Text Available This paper investigates inequality in SO2 and NOX emissions, by observing their extraordinary levels and uneven distribution in China during the period of the 11th and 12th Five-Year Plans (FYPs, 2006–2015. This provincial and regional analysis utilizing the Theil index and Kaya factors help us to find the trajectory of inequality and its primary sources. Based on our analysis, we conclude the driving factors behind emissions inequalities are as follows. There are four economic factors of per capita SO2 emission: SO2 emission intensity of coal consumption, coal intensity of power generation, power intensity of GDP, and per capita GDP. Additionally, there are four urban development factors of per capita NOX emission: NOX emission intensity of gasoline consumption, proportion of gasoline vehicles, vehicle use in urban population, and urbanization rate. The SO2 emission results represent an increase of 6% in overall inequality where the inequality of power intensity of GDP is the main contributor. In terms of NOX emission, the 3% growth in total inequality is related to the high effect of NOX emission intensity of gasoline consumption. We also examine the effect of other factors affecting the trajectory of inequalities. To apply these results in practice, we compare the 11th and 12th FYPs and give some policy suggestions.

  9. Using Himawari-8, estimation of SO2 cloud altitude at Aso volcano eruption, on October 8, 2016

    Science.gov (United States)

    Ishii, Kensuke; Hayashi, Yuta; Shimbori, Toshiki

    2018-02-01

    It is vital to detect volcanic plumes as soon as possible for volcanic hazard mitigation such as aviation safety and the life of residents. Himawari-8, the Japan Meteorological Agency's (JMA's) geostationary meteorological satellite, has high spatial resolution and sixteen observation bands including the 8.6 μm band to detect sulfur dioxide (SO2). Therefore, Ash RGB composite images (RED: brightness temperature (BT) difference between 12.4 and 10.4 μm, GREEN: BT difference between 10.4 and 8.6 μm, BLUE: 10.4 μm) discriminate SO2 clouds and volcanic ash clouds from meteorological clouds. Since the Himawari-8 has also high temporal resolution, the real-time monitoring of ash and SO2 clouds is of great use. A phreatomagmatic eruption of Aso volcano in Kyushu, Japan, occurred at 01:46 JST on October 8, 2016. For this eruption, the Ash RGB could detect SO2 cloud from Aso volcano immediately after the eruption and track it even 12 h after. In this case, the Ash RGB images every 2.5 min could clearly detect the SO2 cloud that conventional images such as infrared and split window could not detect sufficiently. Furthermore, we could estimate the height of the SO2 cloud by comparing the Ash RGB images and simulations of the JMA Global Atmospheric Transport Model with a variety of height parameters. As a result of comparison, the top and bottom height of the SO2 cloud emitted from the eruption was estimated as 7 and 13-14 km, respectively. Assuming the plume height was 13-14 km and eruption duration was 160-220 s (as estimated by seismic observation), the total emission mass of volcanic ash from the eruption was estimated as 6.1-11.8 × 108 kg, which is relatively consistent with 6.0-6.5 × 108 kg from field survey. [Figure not available: see fulltext.

  10. Degassing of CO2, SO2, and H2S associated with the 2009 eruption of Redoubt Volcano, Alaska

    Science.gov (United States)

    Werner, Cynthia; Kelly, Peter J.; Doukas, Michael; Lopez, Taryn; Pfeffer, Melissa; McGimsey, Robert; Neal, Christina

    2013-06-01

    The 2009 eruption of Redoubt Volcano, Alaska was particularly well monitored for volcanic gas emissions. We report 35 airborne measurements of CO2, SO2, and H2S emission rates that span from October 2008 to August 2010. The magmatic system degassed primarily as a closed system although minor amounts of open system degassing were observed in the 6 months prior to eruption on March 15, 2009 and over 1 year following cessation of dome extrusion. Only 14% of the total CO2 was emitted prior to eruption even though high emissions rates (between 3630 and 9020 t/d) were observed in the final 6 weeks preceding the eruption. A minor amount of the total SO2 was observed prior to eruption (4%), which was consistent with the low emission rates at that time (up to 180 t/d). The amount of the gas emitted during the explosive and dome growth period (March 15-July 1, 2009) was 59 and 66% of the total CO2 and SO2, respectively. Maximum emission rates were 33,110 t/d CO2, 16,650 t/d SO2, and 1230 t/d H2S. Post-eruptive passive degassing was responsible for 27 and 30% of the total CO2 and SO2, respectively. SO2 made up on average 92% of the total sulfur degassing throughout the eruption. Magmas were vapor saturated with a C- and S-rich volatile phase, and regardless of composition, the magmas appear to be buffered by a volatile composition with a molar CO2/SO2 ratio of ~ 2.4. Primary volatile contents calculated from degassing and erupted magma volumes range from 0.9 to 2.1 wt.% CO2 and 0.27-0.56 wt.% S; whole-rock normalized values are slightly lower (0.8-1.7 wt.% CO2 and 0.22-0.47 wt.% S) and are similar to what was calculated for the 1989-90 eruption of Redoubt. Such contents argue that primary arc magmas are rich in CO2 and S. Similar trends between volumes of estimated degassed magma and observed erupted magma during the eruptive period point to primary volatile contents of 1.25 wt.% CO2 and 0.35 wt.% S. Assuming these values, up to 30% additional unerupted magma degassed in the

  11. One year observations of atmospheric reactive gases (O3, CO, NOx, SO2) at Jang Bogo base in Terra Nova Bay, Antarctica

    Science.gov (United States)

    Siek Rhee, Tae; Seo, Sora

    2016-04-01

    Antarctica is a remote area surrounded by the Southern Ocean and far from the influence of human activities, giving us unique opportunity to investigate the background variation of trace gases which are sensitive to the human activities. Korean Antarctic base, Jang Bogo, was established as a unique permanent overwintering base in Terra Nova Bay in February, 2014. One year later, we installed a package of instruments to monitor atmospheric trace gases at the base, which includes long-lived greenhouse gases, CO2, CH4, and N2O, and reactive gases, O3, CO, NOx, and SO2. The atmospheric chemistry observatory, where these scientific instruments were installed, is located ca. 1 km far from the main building and power plant, minimizing the influence of pollution that may come from the operation of the base. Here we focus on the reactive gases measured in-situ at the base; O3 displays a typical seasonal variation with high in winter and low in summer with seasonal amplitude of ~18 ppb, CO was high in September at ~56 ppb, probably implying the invasion of lower latitude air mass with biomass burning, and low in late summer due to photochemical oxidation. NO did not show clear seasonal variation, but SO2 reveals larger values in summer than in winter. We will discuss potential atmospheric processes behind these first observations of reactive gases in Terra Nova Bay, Antarctica.

  12. Atmospheric measurements of gas-phase HNO3 and SO2 using chemical ionization mass spectrometry during the MINATROC field campaign 2000 on Monte Cimone

    Directory of Open Access Journals (Sweden)

    M. Hanke

    2003-01-01

    Full Text Available The EU-project MINATROC (MINeral dust And TROpospheric Chemistry aims at enabling an estimation of the influence of mineral dust, a major, but to date largely ignored component of tropospheric aerosol, on tropospheric oxidant cycles. Within the scope of this project continuous atmospheric measurements of gas-phase HNO3 and SO2 were conducted in June and July 2000 at the CNR WMO station, situated on Monte Cimone (MTC (44°11' N --10°42' E, 2165 m asl, Italy. African air transporting dust is occasionally advected over the Mediterranean Sea to the site, thus mineral aerosol emitted from Africa will encounter polluted air masses and provide ideal conditions to study their interactions. HNO3 and SO2 were measured with an improved CIMS (chemical ionization mass spectrometry system for ground-based measurements that was developed and built at MPI-K Heidelberg. Since HNO3  is a very sticky compound special care was paid for the air-sampling and background-measurement system. Complete data sets could be obtained before, during and after major dust intrusions. For the first time these measurements might provide a strong observational indication of efficient uptake of gas-phase HNO3 by atmospheric mineral-dust aerosol particles.

  13. Cognitive Approaches for Medicine in Cloud Computing.

    Science.gov (United States)

    Ogiela, Urszula; Takizawa, Makoto; Ogiela, Lidia

    2018-03-03

    This paper will present the application potential of the cognitive approach to data interpretation, with special reference to medical areas. The possibilities of using the meaning approach to data description and analysis will be proposed for data analysis tasks in Cloud Computing. The methods of cognitive data management in Cloud Computing are aimed to support the processes of protecting data against unauthorised takeover and they serve to enhance the data management processes. The accomplishment of the proposed tasks will be the definition of algorithms for the execution of meaning data interpretation processes in safe Cloud Computing. • We proposed a cognitive methods for data description. • Proposed a techniques for secure data in Cloud Computing. • Application of cognitive approaches for medicine was described.

  14. Security model for VM in cloud

    Science.gov (United States)

    Kanaparti, Venkataramana; Naveen K., R.; Rajani, S.; Padmvathamma, M.; Anitha, C.

    2013-03-01

    Cloud computing is a new approach emerged to meet ever-increasing demand for computing resources and to reduce operational costs and Capital Expenditure for IT services. As this new way of computation allows data and applications to be stored away from own corporate server, it brings more issues in security such as virtualization security, distributed computing, application security, identity management, access control and authentication. Even though Virtualization forms the basis for cloud computing it poses many threats in securing cloud. As most of Security threats lies at Virtualization layer in cloud we proposed this new Security Model for Virtual Machine in Cloud (SMVC) in which every process is authenticated by Trusted-Agent (TA) in Hypervisor as well as in VM. Our proposed model is designed to with-stand attacks by unauthorized process that pose threat to applications related to Data Mining, OLAP systems, Image processing which requires huge resources in cloud deployed on one or more VM's.

  15. MODELING POTENTIAL IMPACTS OF SO2 CO-INJECTED WITH CO2 ON THE KNOX GROUP, WESTERN KENTUCKY

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Junfeng; Harris, David; Leetaru, Hannes

    2014-09-30

    Understanding potential long-term impacts of CO2 impurities, such as sulfur and nitrogen compounds, on deep carbon storage reservoirs is of considerable interest because co-injection of the impurities with CO2 can bring significant economic and environmental benefits. The Cambrian–Ordovician Knox Group, a thick sequence of dolostone (Beekmantown Dolomite) with minor dolomitic sandstone (Gunter Sandstone), in western Kentucky, USA, has been evaluated as a prospective CO2 sequestration target. In this study, TOUGHREACT was used to build 1-D radial models to simulate the potential impacts of co-injected CO2 and SO2 on minerals, pore fluids, and porosity and permeability in the Beekmantown Dolomite and the Gunter Sandstone. Co-injection of a mass ratio of 2.5 percent SO2 and 97.5 percent CO2, representative of flue gas from coal-fired plants, was simulated and the co-injection simulations were compared to models with CO2 only injections. The model results suggest that the major impacts of added SO2 for both the Beekmantown and the Gunter rocks were significant enhancement of dissolution of dolomite and precipitation of anhydrite, leading to noticeable increases in porosity and permeability. The Gunter Sandstone appeared to be more active with SO2 than the Beekmantown Dolomite. More dolomite was dissolved in the Gunter than in the Beekmantown with the same SO2 impurity. Consequently, porosity was raised more in the Gunter than in the Beekmantown. On the other hand, the impacts on aluminosilicate minerals appeared to be insignificant in both reservoirs, slightly changing the rates of precipitation/dissolution but the overall reaction paths remained the same.

  16. Sulfur chemistry in the envelope of VY Canis Majoris: Detailed analysis of SO and SO2 emission

    International Nuclear Information System (INIS)

    Adande, G. R.; Edwards, J. L.; Ziurys, L. M.

    2013-01-01

    Detailed radiative transfer modeling has been carried out for SO 2 and SO originating in the envelope of the O-rich supergiant star VY Canis Majoris (VY CMa). A total of 27 transitions of SO 2 and 7 transitions of SO lying in the energy range 3.0-138.2 cm –1 were analyzed using a new non-LTE radiative transfer code that incorporates non-spherical geometries. The spectra were primarily obtained from the Arizona Radio Observatory (ARO) 1 mm spectral survey of VY CMa, conducted with the Submillimeter Telescope; additional lines were measured with the ARO 12 m antenna at 2 and 3 mm. SO 2 and SO were found to arise from five distinct outflows within the envelope, four which are asymmetric with respect to the star. Three flows arise from high-velocity red-shifted material, one from a blue-shifted wind, and the final from a classic 'spherical' expansion. In the spherical component, the peak fractional abundance, relative to H 2 , of both molecules is f ∼ 2.5 × 10 –7 at r ∼ 25 R * , and steadily decreases outward. SO 2 appears to be a 'parent' molecule, formed near the stellar photosphere. In the asymmetric outflows, both SO and SO 2 are more prominent at large stellar radii in dense (10 6 -10 7 cm –3 ), clumpy material, achieving their maximum abundance between 200 and 600 R * with f ∼ 3.0 × 10 –8 -1.5 × 10 –7 . These results suggest that in the collimated outflows, both species are either produced by shock chemistry or are remnant inner shell material swept up in the high-velocity winds.

  17. SO2 emissions from Popocatépetl volcano: emission rates and plume imaging using optical remote sensing techniques

    Science.gov (United States)

    Grutter, M.; Basaldud, R.; Rivera, C.; Harig, R.; Junkerman, W.; Caetano, E.; Delgado-Granados, H.

    2008-11-01

    Sulfur dioxide emissions from the Popocatépetl volcano in central Mexico were measured during the MILAGRO field campaign in March 2006. A stationary scanning DOAS (Differential Optical Absorption Spectrometer) was used to monitor the SO2 emissions from the volcano and the results were compared with traverses done with a COSPEC from the ground and a DOAS instrument on board an ultra-light aircraft. Daytime evolutions as well as day-to-day variation of the SO2 emissions are reported. A value of 2.45±1.39 Gg/day of SO2 is reported from all the daily averages obtained during the month of March 2006, with large variation in maximum and minimum daily averages of 5.97 and 0.56 Gg/day, respectively. The large short-term fluctuations in the SO2 emissions obtained could be confirmed through 2-D visualizations of the SO2 plume measured with a scanning imaging infrared spectrometer. This instrument, based on the passive detection of thermal radiation from the volcanic gas and analysis with FTIR spectrometry, is used for the first time for plume visualization of a specific volcanic gas. A 48-h forward trajectory analysis indicates that the volcanic plume was predominantly directed towards the Puebla/Tlaxcala region (63%), followed by the Mexico City and Cuernavaca/Cuautla regions with 19 and 18% occurrences, respectively. 25% of the modeled trajectories going towards the Puebla region reached altitudes lower than 4000 m a.s.l. but all trajectories remained over this altitude for the other two regions.

  18. Behaviour of volcanogenic S-bearing compounds (H2S and SO2) in air at Vulcano Island (Aeolian Archipelago, southern Italy)

    Science.gov (United States)

    Caponi, Chiara; Tassi, Franco; Ricci, Andrea; Capecchiacci, Francesco; Venturi, Stefania; Cabassi, Jacopo; Vaselli, Orlando

    2017-04-01

    The main sources of SO2 and H2S in air consist of both natural fluid emissions related to active/quiescent volcanoes and hydrothermal systems, and anthropogenic activities (e.g. gas and oil refineries, steel industries, urban traffic). These gas compounds have a strong impact on air quality, since they are strong toxic and climate forcing agents. Notwithstanding, the behaviour of these S-compounds in air once they are released from the contaminant source(s) is poorly known, due to the scarce available data from thermodynamics and direct measurements. Hydrogen sulfide is considered to be relatively reactive in the atmosphere, being easily oxidized to SO2 by photochemical reactions, even though the efficiency of the H2S to SO2 conversion is significantly lowered under dark, dry and relatively cold conditions, leading to a residence time of H2S in air up to 42 days in winter. In this work, H2S and SO2 measurements in air carried out at the Levante beach (Vulcano Island, Aeolian Archipelago), where a number of hydrothermal fluid discharges consisting of fumaroles and submarine emissions occur, are presented and discussed. These volcanic fluids, characterized by an H2S-rich chemical composition, are released in a close proximity to the touristic village of Vulcano Porto. The measurements were carried out using a Thermo Scientific™ Model 450i Analyzer coupled with a Davis® Vantage Vue weather station (air humidity and temperature, wind direction and speed) in 34 fixed spots and along 8 pathways, selected according to: (i) distance from the contaminant source, (ii) wind direction and (iii) accessibility by car (where the instrument was installed). The main aim was to provide empirical insights on the behavior of these air pollutants in relation to the physical and chemical processes controlling their spatial distribution. The measured data were elaborated using a statistical approach to construct spatial distribution maps and conceptual models able to forecast the

  19. Structural evolution of derived species on FeAl surface exposed to a N2 + SO2 atmosphere: Experimental and theoretical study

    International Nuclear Information System (INIS)

    Espinosa-Medina, M.A.; Liu, H.B.; Canizal, G.; Ascencio, J.A.

    2007-01-01

    Characterizations were performed by scanning electron microscopy analysis with energy dispersive spectrometry and scanning probe microscope for structural evolution of derived species on FeAl surface exposed to a N 2 + SO 2 atmosphere at high temperature. First principle calculations were also employed in order to clarify the formation of new product on the surface and its mechanism. The results demonstrate that the tendency of the structure with oxygen atoms involve a stronger interaction and lower energy to be formed with the surface and consequently the possible production of oxide-species is more probable and multiple aggregates with different shapes can be generated for the temperatures of 625 and 700 deg. C, with no preferential crystal habit. Sample treated at 775 deg. C denotes the production of hexagonal crystals, which is externally characterized by polyhedrons growing in axial direction as fibbers with flat faces that match with the alumina

  20. Estimation of transboundary SO2 fluxes in Siberia and Russian Far East using EANET and OMI observations

    Science.gov (United States)

    Trifonova-Yakovleva, Alisa; Gromov, Sergey S.; Gromov, Sergey A.

    2017-04-01

    Air pollution caused by emissions from industrial and other anthropogenic sources is a long-standing issue for the East Asian region, and will likely remain so in the near future. Being moderately to long-lived, some pollutants survive long-range atmospheric transport and thus are capable of affecting air quality in regions remote to the emission sources. One of problems one may address to quantify this important potential is studying transboundary fluxes of species of interest. Recently the approaches to such problems became more deterministic due to increasingly available data products providing large spatiotemporal coverage, e.g. 3D models and satellite observations. In this study, we quantify the transboundary fluxes of sulphur dioxide (SO2) over the Asian segment of Russian border (shared with Mongolia and China) in 2015. Using the meteorological fields from the ERA INTERIM (EI) re-analysis [1], we calculate the amounts of air transported every 6h in different vertical domains across the border. We reckon that about 5.5•1018 moles of air was transported (net) outwards Russia in the EI-simulated dynamic planetary boundary layer (PBL). We further use the SO2 retrievals products available from the Ozone Monitoring Instrument (OMI, [2]) and the EI data to reconstruct the concomitant mixing ratios of SO2 in the PBL. The convolution of these terms allows to quantify the net transport of SO2 within the PBL, which amounts to not less than (180-190)•103 tons transported inwards Russia in 2015. We find that this result is robust (within ±5•103 tons) when less certain data (e.g. at radiative cloud fraction > 0.2) from OMI PBL SO2 product are included. Similar robustness is seen when the SO2 transport is calculated for the periods when only concomitant satellite data is available (around noon, corresponds to about 17% of total net air transport) and when nearest in time SO2 columns are used for the remaining periods (e.g., night time, about 91% of total net air

  1. SO2 Nonattainment Areas

    Data.gov (United States)

    U.S. Environmental Protection Agency — This data layer identifies areas in the U.S. where air pollution levels have not met the National Ambient Air Quality Standards (NAAQS) for Sulfur dioxide and have...

  2. Analysis of ambient SO2 concentrations and winds in the complex surrounding of a thermal power plant

    International Nuclear Information System (INIS)

    Mlakar, P.

    2004-01-01

    SO 2 pollution is still a significant problem in Slovenia, especially around large thermal power plants (TPPs), like the one at Sostanj. The Sostanj TPP is the exclusive source of SO 2 in the area and is therefore a perfect example for air pollution studies. In order to understand air pollution around the Sostanj TPP in detail, some analyses of emissions and ambient concentrations of SO 2 at six automated monitoring stations in the surrounding of the TPP were made. The data base from 1991 to 1993 was used when there were no desulfurization plants in operations. Statistical analyses of the influence of the emissions from the three TPP stacks at different measuring points were made. The analyses prove that the smallest stack (100 m) mainly pollutes villages and towns near the TPP within a radius of a few kilometers. The medium stack's (150 m) influence is noticed at shorter as well as at longer distances up to more than ten kilometers. The highest stack (230 m) pollutes mainly at longer distances, where the plume reaches the higher hills. Detailed analyses of ambient SO 2 concentrations were made. They show the temporal and spatial distribution of different classes of SO 2 concentrations from very low to alarming values. These analyses show that pollution patterns at a particular station remain the same if observed on a yearly basis, but can vary very much if observed on a monthly basis, mainly because of different weather patterns. Therefore the winds in the basin (as the most important feature influencing air pollution dispersion) were further analysed in detail to find clusters of similar patterns. For cluster analysis of ground-level winds patterns in the basin around the Sostanj Thermal Power Plant, the Kohonen neural network and Leaders' method were used. Furthermore the dependence of ambient SO 2 concentrations on the clusters obtained was analysed. The results proved that effective cluster analysis can be a useful tool for compressing a huge wind data base in

  3. New Insights into the Seismicity and SO2 Degassing at Cotopaxi Volcano (Ecuador) During the 2015 Unrest and Eruptive Period

    Science.gov (United States)

    Hidalgo, S.; Battaglia, J.

    2017-12-01

    Cotopaxi (5897 m) had an unrest and eruption between April and November 2015. Seismic signals and SO2 emissions were recorded by the monitoring network of the Instituto Geofísico. The network includes 11 seismic stations, 6 broad band and 5 short period; and 4 NOVAC-Type 1 DOAS permanent instruments.We reviewed the seismic records to better understand the link between seismicity and SO2 emissions. Transient events detected include Volcano-Tectonic (VT), Long-Period (LP) events and Explosion Quakes (EQ), but also Ice Quakes (IQ) with various spectral signatures related to the glacier covering the volcano summit. An event-per-event exhaustive identification is, however, impossible because of the very large number of events and the wide range of signals, with variable spectral characteristics. Therefore, to identify the different types of events activated previous and during the eruption, we choose an approach based on the search of families of repeating events. Looking at the temporal evolution of these families, we determined 4 characteristic types. The first and more frequent, Type 1, is mainly composed by IQ. Type 2, mainly LPs appeared only in April and May 2015. Interestingly, its rate of occurrence starts increasing the first days of April, is maximum about mid-May when SO2 appears and then progressively drops to totally stop on June 4, replaced by tremor. Since then, and until the hydromagmatic explosions opening the system, SO2 emissions between 3000 and 5000 t/day were directly linked to seismic tremor. Type 3 families, are dominated by VTs, and are only active on 13 and 14 August, before and during the hydromagmatic explosions. These events should be considered as short term seismic precursors. Type 4 families starts at the beginning of September and included only few VTs. Nevertheless, since September, most of the observed events belong to Type 1 families, mainly IQ, hence the seismicity related to volcanic activity after the hydromagmatic explosions was

  4. O3, SO2, NO2, and UVB measurements in Beijing and Baseline Station of northwestern part of China

    Science.gov (United States)

    Guo, Song; Zhou, Xiuji; Zhang, Xiachun

    1994-01-01

    A MKII Brewer ozone spectrometer was used in Beijing from Oct. 1990 to June 1991 to measure O3, SO2 and UVB radiation. And since Nov. 1991 a new MKIV Brewer spectrometer, which can take the measurements of O3, SO2, NO2 and UVB radiation, has been set up in Beijing. The MKII Brewer spectrometer was moved to Qinghai baseline station which is on the Qinghai-tibetean plateau in the northwestern part of China. Both the data in Beijing and Qinghai baseline station has been analyzed and some results will be shown here along with the ozone profiles botained through the Umkehr program given by AES of Canada for the Brewer ozone spectrometer.

  5. Structural Characterization of 1,1,3,3-Tetramethylguanidinium Chloride Ionic Liquid by Reversible SO2 Gas Absorption

    DEFF Research Database (Denmark)

    Berg, Rolf W.; Harris, Pernille; Riisager, Anders

    2013-01-01

    A unique new ionic liquid−gas adduct solid state compound formed between 1,1,3,3-tetramethylguanidinium chloride ([tmgH]Cl) and sulfur dioxide has been characterized by X-ray diffraction and Raman spectroscopy. The structure contains SO2 molecules of near normal structure kept at their positions...... by Cl−S interactions. The crystals belong in the orthorhombic system, space group Pbcn, with unit cell dimensions of a = 15.6908(10) Å, b = 9.3865(6) Å, and c = 14.1494(9) Å, angles α = β = γ = 90°, and Z = 8 at 120 K. The [tmgH]Cl has a very high absorption capacity of nearly 3 mol of SO2 per mol...

  6. Energy Efficiency in Cloud Software Architectures

    NARCIS (Netherlands)

    Procaccianti, G.; Bevini, S.; Lago, P.; Bernd Page, B. P.; Andreas G. Fleischer, A. G. F.; Johannes Gobel, J. G.; Volker Wohlgemuth, V. W.

    2013-01-01

    Cloud-based software is often considered as providing a greener, more energy-efficient solution. At the same time, it introduces more complexity and demands for new investments in cloud services, technologies, and competencies for migration, maintenance, and evolution of the underlying software

  7. Improved Satellite Retrievals of NO2 and SO2 over the Canadian Oil Sands and Comparisons with Surface Measurements

    Science.gov (United States)

    McLinden, C. A.; Fioletov, V.; Boersma, K. F.; Kharol, S. K.; Krotkov, N.; Lamsal, L.; Makar, P. A.; Martin, R. V.; Veefkind, J. P.; Yang, K.

    2014-01-01

    Satellite remote sensing is increasingly being used to monitor air quality over localized sources such as the Canadian oil sands. Following an initial study, significantly low biases have been identified in current NO2 and SO2 retrieval products from the Ozone Monitoring Instrument (OMI) satellite sensor over this location resulting from a combination of its rapid development and small spatial scale. Air mass factors (AMFs) used to convert line-of-sight "slant" columns to vertical columns were re-calculated for this region based on updated and higher resolution input information including absorber profiles from a regional-scale (15 km × 15 km resolution) air quality model, higher spatial and temporal resolution surface reflectivity, and an improved treatment of snow. The overall impact of these new Environment Canada (EC) AMFs led to substantial increases in the peak NO2 and SO2 average vertical column density (VCD), occurring over an area of intensive surface mining, by factors of 2 and 1.4, respectively, relative to estimates made with previous AMFs. Comparisons are made with long-term averages of NO2 and SO2 (2005-2011) from in situ surface monitors by using the air quality model to map the OMI VCDs to surface concentrations. This new OMI-EC product is able to capture the spatial distribution of the in situ instruments (slopes of 0.65 to 1.0, correlation coefficients of greater than 0.9). The concentration absolute values from surface network observations were in reasonable agreement, with OMI-EC NO2 and SO2 biased low by roughly 30%. Several complications were addressed including correction for the interference effect in the surface NO2 instruments and smoothing and clear-sky biases in the OMI measurements. Overall these results highlight the importance of using input information that accounts for the spatial and temporal variability of the location of interest when performing retrievals.

  8. Cleaning up the air: effectiveness of air quality policy for SO2 and NOx emissions in China

    Science.gov (United States)

    van der A, Ronald J.; Mijling, Bas; Ding, Jieying; Elissavet Koukouli, Maria; Liu, Fei; Li, Qing; Mao, Huiqin; Theys, Nicolas

    2017-02-01

    Air quality observations by satellite instruments are global and have a regular temporal resolution, which makes them very useful in studying long-term trends in atmospheric species. To monitor air quality trends in China for the period 2005-2015, we derive SO2 columns and NOx emissions on a provincial level with improved accuracy. To put these trends into perspective they are compared with public data on energy consumption and the environmental policies of China. We distinguish the effect of air quality regulations from economic growth by comparing them relatively to fossil fuel consumption. Pollutant levels, per unit of fossil fuel, are used to assess the effectiveness of air quality regulations. We note that the desulfurization regulations enforced in 2005-2006 only had a significant effect in the years 2008-2009, when a much stricter control of the actual use of the installations began. For national NOx emissions a distinct decreasing trend is only visible from 2012 onwards, but the emission peak year differs from province to province. Unlike SO2, emissions of NOx are highly related to traffic. Furthermore, regulations for NOx emissions are partly decided on a provincial level. The last 3 years show a reduction both in SO2 and NOx emissions per fossil fuel unit, since the authorities have implemented several new environmental regulations. Despite an increasing fossil fuel consumption and a growing transport sector, the effects of air quality policy in China are clearly visible. Without the air quality regulations the concentration of SO2 would be about 2.5 times higher and the NO2 concentrations would be at least 25 % higher than they are today in China.

  9. Particulate sulfate ion concentration and SO2 emission trends in the United States from the early 1990s through 2010

    Directory of Open Access Journals (Sweden)

    W. C. Malm

    2012-11-01

    Full Text Available We examined particulate sulfate ion concentrations across the United States from the early 1990s through 2010 using remote/rural data from the Interagency Monitoring of Protected Visual Environments (IMPROVE network and from early 2000 through 2010 using data from the Environmental Protection Agency's (EPA urban Chemical Speciation Network (CSN. We also examined measured sulfur dioxide (SO2 emissions from power plants from 1995 through 2010 from the EPA's Acid Rain Program. The 1992–2010 annual mean sulfate concentrations at long-term rural sites in the United States have decreased significantly and fairly consistently across the United States at a rate of −2.7% yr−1 (p −1 (p −1 (p 2 emissions from power plants across the United States have decreased at a similar rate as sulfate concentrations from 2001 to 2010 (−6.2% yr−1, p 2 emissions and average sulfate concentrations. This linearity was strongest in the eastern United States and weakest in the West where power plant SO2 emissions were lowest and sulfate concentrations were more influenced by non-power-plant and perhaps international SO2 emissions. In addition, annual mean, short-term sulfate concentrations decreased more rapidly in the East relative to the West due to differences in seasonal trends at certain regions in the West. Specifically, increased wintertime concentrations in the central and northern Great Plains and increased springtime concentrations in the western United States were observed. These seasonal and regional positive trends could not be explained by changes in known local and regional SO2 emissions, suggesting other contributing influences. This work implies that on an annual mean basis across the United States, air quality mitigation strategies have been successful in reducing the particulate loading of sulfate in the atmosphere; however, for certain seasons and regions, especially in the West, current mitigation strategies appear insufficient.

  10. Simulations of the Holuhraun eruption 2014 with WRF-Chem and evaluation with satellite and ground based SO2 measurements

    Science.gov (United States)

    Hirtl, Marcus; Arnold-Arias, Delia; Flandorfer, Claudia; Maurer, Christian; Mantovani, Simone; Natali, Stefano

    2016-04-01

    Volcanic eruptions, with gas or/and particle emissions, directly influence our environment, with special significance when they either occur near inhabited regions or are transported towards them. In addition to the well-known affectation of air traffic, with large economic impacts, the ground touching plumes can lead directly to an influence of soil, water and even to a decrease of air quality. The eruption of Holuhraun in August 2014 in central Iceland is the country's largest lava and gas eruption since the Lakagígar eruption in 1783. Nevertheless, very little volcanic ash was produced. The main atmospheric threat from this event was the SO2 pollution that frequently violated the Icelandic National Air Quality Standards in many population centers. However, the SO2 affectation was not limited to Iceland but extended to mainland Europe. The on-line coupled model WRF-Chem is used to simulate the dispersion of SO2 for this event that affected the central European regions. The volcanic emissions are considered in addition to the anthropogenic and biogenic ground sources at European scale. A modified version of WRF-Chem version 4.1 is used in order to use time depending injection heights and mass fluxes which were obtained from in situ observations. WRF-Chem uses complex gas- (RADM2) and aerosol- (MADE-SORGAM) chemistry and is operated on a European domain (12 km resolution), and a nested grid covering the Alpine region (4 km resolution). The study is showing the evaluation of the model simulations with satellite and ground based measurement data of SO2. The analysis is conducted on a data management platform, which is currently developed in the frame of the ESA-funded project TAMP "Technology and Atmospheric Mission Platform": it provides comprehensive functionalities to visualize and numerically compare data from different sources (model, satellite and ground-measurements).

  11. Dynamical symmetry as a tool to understanding properties of supersymmetric partner potentials. Example of so(2,1) symmetry

    International Nuclear Information System (INIS)

    Wehrhahn, R.F.; Cooper, I.L.

    1992-05-01

    Analysis of the dynamical symmetry of a system is used to predict properties arising from its supersymmetric quantum mechanical treatment. Two applications of the so(2,1) algebra, the Coulomb potential and Morse oscillator potential which display different structure with respect to the dynamical symmetry, are studied. This difference is shown to be responsible for the behaviour of the respective supersymmetric partner potentials. (orig.)

  12. A risk assessment of potential agricultural losses due to ambient SO2 in the central regions of Chile

    International Nuclear Information System (INIS)

    Garcia-Huidobro, T.; Marshall, F.M.; Bell, J.N.B.

    2001-01-01

    A risk assessment of the potential impacts of sulphur dioxide (SO 2 ) on the agriculture of central Chile was carried out, using Critical Levels (threshold values above which chronic effects may occur) set by the United Nations Economic Commission for Europe (UNECE, 1993; Sanders et al., 1995), crop sensitivity studies, agricultural land-use data, and air quality data for several years. Ambient SO 2 concentrations around three copper smelters in this region were found to pose a significant risk to crops (such as cereals, staples and legumes) on both local and regional scales. Adverse effects on yield, growth and fruit production were considered possible. Frequent high exposure periods during winter months may also give rise to acute injury in sensitive species and/or crops maintained under optimum water conditions. This study identified high-risk areas, where additional monitoring as well as field studies would be beneficial, and has important policy implications, given the secondary SO 2 air quality standard currently in force in Chile. (Author)

  13. Effects of SO2 on selective catalytic reduction of NO with NH3 over a TiO2 photocatalyst

    International Nuclear Information System (INIS)

    Yamamoto, Akira; Teramura, Kentaro; Hosokawa, Saburo; Tanaka, Tsunehiro

    2015-01-01

    The effect of SO 2 gas was investigated on the activity of the photo-assisted selective catalytic reduction of nitrogen monoxide (NO) with ammonia (NH 3 ) over a TiO 2 photocatalyst in the presence of excess oxygen (photo-SCR). The introduction of SO 2 (300 ppm) greatly decreased the activity of the photo-SCR at 373 K. The increment of the reaction temperature enhanced the resistance to SO 2 gas, and at 553 K the conversion of NO was stable for at least 300 min of the reaction. X-ray diffraction, FTIR spectroscopy, thermogravimetry and differential thermal analysis, x-ray photoelectron spectroscopy (XPS), elemental analysis and N 2 adsorption measurement revealed that the ammonium sulfate species were generated after the reaction. There was a strong negative correlation between the deposition amount of the ammonium sulfate species and the specific surface area. Based on the above relationship, we concluded that the deposition of the ammonium sulfate species decreased the specific surface area by plugging the pore structure of the catalyst, and the decrease of the specific surface area resulted in the deactivation of the catalyst. (focus issue paper)

  14. Effects of SO2 on selective catalytic reduction of NO with NH3 over a TiO2 photocatalyst

    Science.gov (United States)

    Yamamoto, Akira; Teramura, Kentaro; Hosokawa, Saburo; Tanaka, Tsunehiro

    2015-04-01

    The effect of SO2 gas was investigated on the activity of the photo-assisted selective catalytic reduction of nitrogen monoxide (NO) with ammonia (NH3) over a TiO2 photocatalyst in the presence of excess oxygen (photo-SCR). The introduction of SO2 (300 ppm) greatly decreased the activity of the photo-SCR at 373 K. The increment of the reaction temperature enhanced the resistance to SO2 gas, and at 553 K the conversion of NO was stable for at least 300 min of the reaction. X-ray diffraction, FTIR spectroscopy, thermogravimetry and differential thermal analysis, x-ray photoelectron spectroscopy (XPS), elemental analysis and N2 adsorption measurement revealed that the ammonium sulfate species were generated after the reaction. There was a strong negative correlation between the deposition amount of the ammonium sulfate species and the specific surface area. Based on the above relationship, we concluded that the deposition of the ammonium sulfate species decreased the specific surface area by plugging the pore structure of the catalyst, and the decrease of the specific surface area resulted in the deactivation of the catalyst.

  15. A quasi-classical study of energy transfer in collisions of hyperthermal H atoms with SO2 molecules.

    Science.gov (United States)

    da Silva, Ramon S; Garrido, Juan D; Ballester, Maikel Y

    2017-08-28

    A deep understanding of energy transfer processes in molecular collisions is at central attention in physical chemistry. Particularly vibrational excitation of small molecules colliding with hot light atoms, via a metastable complex formation, has shown to be an efficient manner of enhancing reactivity. A quasi-classical trajectory study of translation-to-vibration energy transfer (T-V ET) in collisions of hyperthermal H( 2 S) atoms with SO 2 (X̃ 1 A ' ) molecules is presented here. For such a study, a double many-body expansion potential energy surface previously reported for HSO 2 ( 2 A) is used. This work was motivated by recent experiments by Ma et al. studying collisions of H + SO 2 at the translational energy of 59 kcal/mol [J. Ma et al., Phys. Rev. A 93, 040702 (2016)]. Calculations reproduce the experimental evidence that during majority of inelastic non-reactive collision processes, there is a metastable intermediate formation (HOSO or HSO 2 ). Nevertheless, the analysis of the trajectories shows that there are two distinct mechanisms in the T-V ET process: direct and indirect. Direct T-V processes are responsible for the high population of SO 2 with relatively low vibrational excitation energy, while indirect ones dominate the conversion from translational energy to high values of the vibrational counterpart.

  16. A Decade of Change in NO2 and SO2 over the Canadian Oil Sands As Seen from Space

    Science.gov (United States)

    Mclinden, Chris A.; Fioletov, Vitali; Krotkov, Nickolay A.; Li, Can; Boersma, K. Folkert; Adams, Cristen

    2015-01-01

    A decade (20052014) of observations from the Ozone Monitoring Instrument (OMI) were used to examine trends in nitrogen dioxide(NO2) and sulfur dioxide (SO2) over a large region of western Canada and the northern United States, with a focus on the Canadian oil sands. In the oil sands, primarily over an area of intensive surface mining, NO2 tropospheric vertical column densities (VCDs) are seen to be increasing by as much as 10year, with the location of the largest trends in a newly developing NO2 lobe well removed from surface monitoring stations. SO2 VCDs in the oil sands have remained approximately constant. The only other significant increase in the region was seen in NO2 over Bakken gas fields in North Dakota which showed increases of up to5yr. By contrast, other locations in the region show substantial declines in both pollutants, providing strong evidence to the efficacy of environmental pollution control measures implemented by both nations. The OMI-derived trends were found to be consistent with those from the Canadian surface monitoring network, although in the case of SO2, it was necessary to apply a correction in order to remove the residual signal from volcanic eruptions present in the OMI data.

  17. SO 2 flux from Stromboli during the 2007 eruption: Results from the FLAME network and traverse measurements

    Science.gov (United States)

    Burton, M. R.; Caltabiano, T.; Murè, F.; Salerno, G.; Randazzo, D.

    2009-05-01

    SO 2 fluxes emitted by Stromboli during the 27th February-2nd April 2007 effusive eruption were regularly measured both by an automatic network of scanning ultraviolet spectrometers and by traverse measurements conducted by boat and helicopter. The results from both methodologies agree reasonably well, providing a validation for the automatic flux calculations produced by the network. Approximately 22,000 t of SO 2 were degassed during the course of the 35 day eruption at an average rate of 620 t per day. Such a degassing rate is much higher than that normally observed (150-200 t/d), because the cross-sectional area occupied by ascending degassed magma is much greater than normal during the effusion, as descending, degassed magma that would normally occupy a large volume of the conduit is absent. We propose that the hydrostatically controlled magma level within Stromboli's conduit is the main control on eruptive activity, and that a high effusion rate led to the depressurisation of an intermediate magma reservoir, creating a decrease in the magma level until it dropped beneath the eruptive fissure, causing the rapid end of the eruption. A significant decrease in SO 2 flux was observed prior to a paroxysm on 15th March 2007, suggesting that choking of the gas flowing in the conduit may have induced a coalescence event, and consequent rapid ascent of gas and magma that produced the explosion.

  18. OMPS-NPP L2 NM Sulfur Dioxide (SO2) Total and Tropospheric Column swath orbital V2 (OMPS_NPP_NMSO2_L2) at GES DISC

    Data.gov (United States)

    National Aeronautics and Space Administration — The OMPS-NPP L2 NM Sulfur Dioxide (SO2) Total and Tropospheric Column swath orbital collection 2 version 2.0 product contains the retrieved sulfur dioxide (SO2)...

  19. Adoption of Emissions Abating Technologies by U.S. Electricity Producing Firms Under the SO2 Emission Allowance Market

    Science.gov (United States)

    Creamer, Gregorio Bernardo

    The objective of this research is to determine the adaptation strategies that coal-based, electricity producing firms in the United States utilize to comply with the emission control regulations imposed by the SO2 Emissions Allowance Market created by the Clean Air Act Amendment of 1990, and the effect of market conditions on the decision making process. In particular, I take into consideration (1) the existence of carbon contracts for the provision of coal that may a affect coal prices at the plant level, and (2) local and geographical conditions, as well as political arrangements that may encourage firms to adopt strategies that appear socially less efficient. As the electricity producing sector is a regulated sector, firms do not necessarily behave in a way that maximizes the welfare of society when reacting to environmental regulations. In other words, profit maximization actions taken by the firm do not necessarily translate into utility maximization for society. Therefore, the environmental regulator has to direct firms into adopting strategies that are socially efficient, i.e., that maximize utility. The SO 2 permit market is an instrument that allows each firm to reduce marginal emissions abatement costs according to their own production conditions and abatement costs. Companies will be driven to opt for a cost-minimizing emissions abatement strategy or a combination of abatement strategies when adapting to new environmental regulations or markets. Firms may adopt one or more of the following strategies to reduce abatement costs while meeting the emission constraints imposed by the SO2 Emissions Allowance Market: (1) continue with business as usual on the production site while buying SO2 permits to comply with environmental regulations, (2) switch to higher quality, lower sulfur coal inputs that will generate less SO2 emissions, or (3) adopting new emissions abating technologies. A utility optimization condition is that the marginal value of each input

  20. Emission of gas and atmospheric dispersion of SO2 during the December 2013 eruption at San Miguel volcano (El Salvador)

    Science.gov (United States)

    Salerno, Giuseppe G.; Granieri, Domenico; Liuzzo, Marco; La Spina, Alessandro; Giuffrida, Giovanni B.; Caltabiano, Tommaso; Giudice, Gaetano; Gutierrez, Eduardo; Montalvo, Francisco; Burton, Michael; Papale, Paolo

    2016-04-01

    San Miguel volcano, also known as Chaparrastique, is a basaltic volcano along the Central American Volcanic Arc (CAVA). Volcanism is induced by the convergence of the Cocos Plate underneath the Caribbean Plate, along a 1200-km arc, extending from Guatemala to Costa Rica and parallel to the Central American Trench. The volcano is located in the eastern part of El Salvador, in proximity to the large communities of San Miguel, San Rafael Oriente, and San Jorge. Approximately 70,000 residents, mostly farmers, live around the crater and the city of San Miguel, the second largest city of El Salvador, ten km from the summit, has a population of ~180,000 inhabitants. The Pan-American and Coastal highways cross the north and south flanks of the volcano.San Miguel volcano has produced modest eruptions, with at least 28 VEI 1-2 events between 1699 and 1967 (datafrom Smithsonian Institution http://www.volcano.si.edu/volcano.cfm?vn=343100). It is characterized by visible milddegassing from a summit vent and fumarole field, and by intermittent lava flows and Strombolian activity. Since the last vigorous fire fountaining of 1976, San Miguel has only experienced small steam explosions and gas emissions, minor ash fall and rock avalanches. On 29 December 2013 the volcano erupted producing an eruption that has been classified as VEI 2. While eruptions tend to be low-VEI, the presence of major routes and the dense population in the surrounding of the volcano increases the risk that weak explosions with gas and/or ash emission may pose. In this study, we present the first inventory of SO2, CO2, HCl, and HF emission rates on San Miguel volcano, and an analysis of the hazard from volcanogenic SO2 discharged before, during, and after the December 2013 eruption. SO2 was chosen as it is amongst the most critical volcanogenic pollutants, which may cause acute and chronicle disease to humans. Data were gathered by the geochemical monitoring network managed by the Ministerio de Medio Ambiente

  1. Degassing of CO2, SO2, and H2S associated with the 2009 eruption of Redoubt Volcano, Alaska

    Science.gov (United States)

    Werner, Cynthia A.; Kelly, Peter; Doukas, Michael P.; Lopez, Taryn; Pfeffer, Melissa; McGimsey, Robert G.; Neal, Christina

    2013-01-01

    The 2009 eruption of Redoubt Volcano, Alaska was particularly well monitored for volcanic gas emissions. We report 35 airborne measurements of CO2, SO2, and H2S emission rates that span from October 2008 to August 2010. The magmatic system degassed primarily as a closed system although minor amounts of open system degassing were observed in the 6 months prior to eruption on March 15, 2009 and over 1 year following cessation of dome extrusion. Only 14% of the total CO2 was emitted prior to eruption even though high emissions rates (between 3630 and 9020 t/d) were observed in the final 6 weeks preceding the eruption. A minor amount of the total SO2 was observed prior to eruption (4%), which was consistent with the low emission rates at that time (up to 180 t/d). The amount of the gas emitted during the explosive and dome growth period (March 15–July 1, 2009) was 59 and 66% of the total CO2and SO2, respectively. Maximum emission rates were 33,110 t/d CO2, 16,650 t/d SO2, and 1230 t/d H2S. Post-eruptive passive degassing was responsible for 27 and 30% of the total CO2 and SO2, respectively. SO2 made up on average 92% of the total sulfur degassing throughout the eruption. Magmas were vapor saturated with a C- and S-rich volatile phase, and regardless of composition, the magmas appear to be buffered by a volatile composition with a molar CO2/SO2 ratio of ~ 2.4. Primary volatile contents calculated from degassing and erupted magma volumes range from 0.9 to 2.1 wt.% CO2 and 0.27–0.56 wt.% S; whole-rock normalized values are slightly lower (0.8–1.7 wt.% CO2 and 0.22–0.47 wt.% S) and are similar to what was calculated for the 1989–90 eruption of Redoubt. Such contents argue that primary arc magmas are rich in CO2 and S. Similar trends between volumes of estimated degassed magma and observed erupted magma during the eruptive period point to primary volatile contents of 1.25 wt.% CO2 and 0.35 wt.% S. Assuming these values, up to 30% additional

  2. Ozone Monitoring Instrument Observations of Interannual Increases in SO2 Emissions from Indian Coal-fired Power Plants During 2005-2012

    Science.gov (United States)

    Lu, Zifeng; Streets, David D.; de Foy, Benjamin; Krotkov, Nickolay A.

    2014-01-01

    Due to the rapid growth of electricity demand and the absence of regulations, sulfur dioxide (SO2) emissions from coal-fired power plants in India have increased notably in the past decade. In this study, we present the first interannual comparison of SO2 emissions and the satellite SO2 observations from the Ozone Monitoring Instrument (OMI) for Indian coal-fired power plants during the OMI era of 2005-2012. A detailed unit-based inventory is developed for the Indian coal-fired power sector, and results show that its SO2 emissions increased dramatically by 71 percent during 2005-2012. Using the oversampling technique, yearly high-resolution OMI maps for the whole domain of India are created, and they reveal a continuous increase in SO2 columns over India. Power plant regions with annual SO2 emissions greater than 50 Gg year-1 produce statistically significant OMI signals, and a high correlation (R equals 0.93) is found between SO2 emissions and OMI-observed SO2 burdens. Contrary to the decreasing trend of national mean SO2 concentrations reported by the Indian Government, both the total OMI-observed SO2 and average SO2 concentrations in coal-fired power plant regions increased by greater than 60 percent during 2005-2012, implying the air quality monitoring network needs to be optimized to reflect the true SO2 situation in India.

  3. Model study of multiphase DMS oxidation with a focus on halogens

    Directory of Open Access Journals (Sweden)

    R. von Glasow

    2004-01-01

    Full Text Available We studied the oxidation of dimethylsulfide (DMS in the marine boundary layer (MBL with a one-dimensional numerical model and focused on the influence of halogens. Our model runs show that there is still significant uncertainty about the end products of the DMS addition pathway, which is especially caused by uncertainty in the product yield of the reaction of the intermediate product methyl sulfinic acid (MSIA with OH. BrO strongly increases the importance of the addition branch in the oxidation of DMS even when present at mixing ratios smaller than 0.5pmol mol-1. The inclusion of halogen chemistry leads to higher DMS oxidation rates and smaller DMS to SO2 conversion efficiencies. The DMS to SO2 conversion efficiency is also drastically reduced under cloudy conditions. In cloud-free model runs between 5 and 15% of the oxidized DMS reacts further to particulate sulfur, in cloudy runs this fraction is almost 100%. Sulfate production by HOClaq and HOBraq is important in cloud droplets even for small Br- deficits and related small gas phase halogen concentrations. In general, more particulate sulfur is formed when halogen chemistry is included. A possible enrichment of HCO3- in fresh sea salt aerosol would increase pH values enough to make the reaction of S(IV* (=SO2,aq+HSO3-+SO32- with O3 dominant for sulfate production. It leads to a shift from methyl sulfonic acid (MSA to non-sea salt sulfate (nss-SO42- production but increases the total nss-SO42- only somewhat because almost all available sulfur is already oxidized to particulate sulfur in the base scenario. We discuss how realistic this is for the MBL. We found the reaction MSAaq+OH to contribute about 10% to the production of nss-SO42- in clouds. It is unimportant for cloud-free model runs. Overall we find that the presence of halogens leads to processes that decrease the albedo of stratiform clouds in the MBL.

  4. Control of SO2 and NOx emissions from fossil fuel-fired power plants: Research and practice of TPRI

    International Nuclear Information System (INIS)

    Ming-Chuan Zhang.

    1993-01-01

    The generation of electric power in China has been dominated by coal for many years. By the end of 1990, total installed generating capacity reached 135 GW, of which fossil fuel-fired plants accounted for 74 percent. The total electricity generated reached 615 TWh, with fossil fuels accounting for 80.5 percent. About 276 million tons of raw coal are consumed in these fossil fuel-burning units per year, accounting for about 25 percent of the total output of the country. According to the government, by the year 2000, the total installed capacity of Chinese power systems should be at least 240 GW, of which fossil fuels will account for about 77 percent. The coal required for power generation will increase to about 530 million tons per year, accounting for about 38 percent of the total coal output. So, it is obvious that coal consumed in coal-fired power plants occupies a very important place in the national fuel balance. The current environmental protection standards, which are based on ground-level concentrations of pollutants, do not effectively lead to the control of pollution emission concentrations or total SO 2 emissions. Due to the practical limitations of the Chinese economy, there is a limited capability to introduce advanced sulfur emission control technologies. Thus, except for the two 360 MW units imported from Japan for the Luohuang Power Plant in Shichuan province, all the other fossil fuel-fired units have not yet adopted any kind of SO 2 removal measures. The Luohuang units are equipped with Mitsubishi limestone flue gas desulfurization systems. Because of the lack of effective pollution control technologies, large areas of the country have been seriously polluted by SO 2 , and some of them even by acid rain

  5. Exploring atmospheric boundary layer characteristics in a severe SO2 episode in the north-eastern Adriatic

    Directory of Open Access Journals (Sweden)

    Z. B. Klaić

    2009-07-01

    Full Text Available Stable atmospheric conditions are often connected with the occurrence of high pollution episodes especially in urban or industrial areas. In this work we investigate a severe SO2 episode observed on 3–5 February 2002 in a coastal industrial town of Rijeka, Croatia, where very high daily mean concentrations (up to 353.5 μg m−3 were measured. The episode occurred under high air pressure conditions, which were accompanied with a fog and low wind speeds. Three air quality models (50-km EMEP model, 10-km EMEP4HR model and 1-km CAMx model were used to simulate SO2 concentrations fields and to evaluate the relative contribution of distant and local pollution sources to observed concentrations. Results suggest that the episode was caused predominately by local sources. Furthermore, using three-dimensional, higher-order turbulence closure mesoscale meteorological model (WRF, the wind regimes and thermo-dynamical structure of the lower troposphere above the greater Rijeka area (GRA were examined in detail. Modelled atmospheric fields suggest several factors whose simultaneous acting was responsible for elevated SO2 concentrations. Established small scale wind directions supported the transport of air from nearby industrial areas with major pollution sources towards Rijeka. This transport was associated with strong, ground-based temperature inversion and correspondingly, very low mixing layer (at most up to about 140 m. Additionally, the surface winds in Rijeka were light or almost calm thus, preventing ventilation of polluted air. Finally, a vertical circulation cell formed between the mainland and a nearby island, supported the air subsidence and the increase of static stability.

  6. UV photoabsorption cross sections of CO, N2, and SO2 for studies of the ISM and planetary atmospheres

    Science.gov (United States)

    Smith, Peter L.; Rufus, J.; Yoshino, K.; Parkinson, W. H.; Stark, Glenn; Pickering, Juliet C.; Thorne, A. P.

    2002-01-01

    We report high-resolution laboratory measurements of photoabsorption cross sections of CO, N2, and SO2 in the wavelength range 80 to 320 nm. The motivation is to provide the quantitative data that are needed to analyze observations of absorption by, and to model photochemical processes in, the interstellar medium and a number of planetary atmospheres. Because of the high resolution of the spectrometers used, we can minimize distortion of the spectrum that occurs when instrument widths are greater than the widths of spectral features being measured. In many cases, we can determine oscillator strengths of individual rotational lines - a unique feature of our work.

  7. Corrosion of Pipeline and Wellbore Steel by Liquid CO2 Containing Trace Amounts of Water and SO2

    Science.gov (United States)

    McGrail, P.; Schaef, H. T.; Owen, A. T.

    2009-12-01

    Carbon dioxide capture and storage in deep saline formations is currently considered the most attractive option to reduce greenhouse gas emissions with continued use of fossil fuels for energy production. Transporting captured CO2 and injection into suitable formations for storage will necessarily involve pipeline systems and wellbores constructed of carbon steels. Industry standards currently require nearly complete dehydration of liquid CO2 to reduce corrosion in the pipeline transport system. However, it may be possible to establish a corrosion threshold based on H2O content in the CO2 that could allow for minor amounts of H2O to remain in the liquid CO2 and thereby eliminate a costly dehydration step. Similarly, trace amounts of sulfur and nitrogen compounds common in flue gas streams are currently removed through expensive desulfurization and catalytic reduction processes. Provided these contaminants could be safely and permanently transported and stored in the geologic reservoir, retrofits of existing fossil-fuel plants could address comprehensive emissions reductions, including CO2 at perhaps nearly the same capital and operating cost. Because CO2-SO2 mixtures have never been commercially transported or injected, both experimental and theoretical work is needed to understand corrosion mechanisms of various steels in these gas mixtures containing varying amounts of water. Experiments were conducted with common tool steel (AISI-01) and pipeline steel (X65) immersed in liquid CO2 at room temperature containing ~1% SO2 and varying amounts of H2O (0 to 2500 ppmw). A threshold concentration of H2O in the liquid CO2-SO2 mixture was established based on the absence of visible surface corrosion. For example, experiments exposing steel to liquid CO2-SO2 containing ~300 ppmw H2O showed a delay in onset of visible corrosion products and minimal surface corrosion was visible after five days of testing. However increasing the water content to 760 ppmw produced extensive

  8. Finding regions of influence on SO2 and SO=4 daily concentration measurements at four sites in Spain

    Directory of Open Access Journals (Sweden)

    E. Hernández

    1996-08-01

    Full Text Available Contamination by the pollutants SO2 and SO=4 was analyzed for the 1989–1992 period at four regional stations in Spain under the auspices of the EMEP-BAPMON program. The evolution of the time series of the daily pollution has also been assessed, and high mean concentrations at La Cartuja and Logroño observed, with values of 3.8 and 4.5 μg m–3 for SO2, respectively. Maximum annual concentrations were recorded in 1989, when SO2 reached values of 6.24, 5.39, 5.71, and 9.30 μg m–3 for the stations of La Cartuja, San Pablo de los Montes, Roquetas, and Logroño, respectively. This work attempts to establish a relationship between the concentrations of the pollutants – both SO2 gas and SO=4 aerosol – and the zones of emission or persistence of these long-range transported pollutants. In this way, those regions showing a greater impact on the air quality in each season have been determined. To achieve this, the trajectories of the air masses carrying away the pollution to each of the receiving stations were considered and followed by a sectorial analysis. Nonparametric statistical methods were implemented to contrast the chemical homogeneity among the different sectors. The criterion that several homogeneous sectors form a chemically homogeneous region was used. To improve this sectorial analysis, we have proposed a new technique based on the Potential-Source-Contribution Function (PSCF. Starting out from a set of specified regions, considered to be chemically homogeneous domains, it is possible to determine the likelihood that an air mass with particular characteristics (e.g., that a value of the daily concentration higher than the mean recorded at the station has been obtained will arrive at a given station after having crossed one of the previously defined regions. Using this technique, it is possible to determine the source regions through which the air masses circulate and bring high pollution concentrations to the studied stations

  9. Privacy and legal issues in cloud computing

    CERN Document Server

    Weber, Rolf H

    2015-01-01

    Adopting a multi-disciplinary and comparative approach, this book focuses on emerging and innovative attempts to tackle privacy and legal issues in cloud computing, such as personal data privacy, security and intellectual property protection. Leading international academics and practitioners in the fields of law and computer science examine the specific legal implications of cloud computing pertaining to jurisdiction, biomedical practice and information ownership. This collection offers original and critical responses to the rising challenges posed by cloud computing.

  10. MULTI TENANCY SECURITY IN CLOUD COMPUTING

    OpenAIRE

    Manjinder Singh*, Charanjit Singh

    2017-01-01

    The word Cloud is used as a metaphor for the internet, based on standardised use of a cloud like shape to denote a network. Cloud Computing is advanced technology for resource sharing through network with less cost as compare to other technologies. Cloud infrastructure supports various models IAAS, SAAS, PAAS. The term virtualization in cloud computing is very useful today. With the help of virtualization, more than one operating system is supported with all resources on single H/W. We can al...

  11. Pricing Schemes in Cloud Computing: An Overview

    OpenAIRE

    Artan Mazrekaj; Isak Shabani; Besmir Sejdiu

    2016-01-01

    Cloud Computing is one of the technologies with rapid development in recent years where there is increasing interest in industry and academia. This technology enables many services and resources for end users. With the rise of cloud services number of companies that offer various services in cloud infrastructure is increased, thus creating a competition on prices in the global market. Cloud Computing providers offer more services to their clients ranging from infrastructure as a service (IaaS...

  12. IP Telephony Applicability in Cloud Computing

    Directory of Open Access Journals (Sweden)

    Francisco Palacios

    2018-02-01

    Full Text Available This paper carries out a research related to the applicability of VoIP over Cloud Computing to guarantee service stability and elasticity of the organizations. In this paper, Elastix is used as an open source software that allows the management and control of a Private Branch Exchange (PBX; and for developing, it is used the services given Amazon Web Services due to their leadership and experience in cloud computing providing security, scalability, backup service and feasibility for the users.

  13. The effect of pre-treatments to the nickel limonite leaching using dissolved gaseous SO2-air

    Science.gov (United States)

    Wulandari, W.; Soerawidjaja, T. H.; Alifiani, D.; Rangga, D. A.

    2018-01-01

    Nickel limonite leaching has been subjected to a number of studies, one of the method is by using dissolved gaseous SO2-air. The selectivity of nickel over iron extracted from leaching using dissolved gaseous SO2-air is advantageous, however the nickel that can be recovered is limited. This paper studies pre-treatments that is applied to the nickel ore prior leaching in order to increase the recovery of dissolved nickel from nickel limonite ore. There two pre-treatments that were carried out in this research, roasting and alkali-roasting using Na2CO3. The extraction was carried out for 180 min with pH 2, 3, 4, and 5 and temperature 30, 55, and 80 °C. It is found that the highest yield is achieved at pH 2 and 80 °C with nickel recovery of 61.39%. At pH 2, for alkali-roasting pre-treatment, the nickel yield raised from 28.17% to 100% and for roasting pre-treatment the nickel yield increased from 20.42% to 61.39%. However, at pH 2, the nickel to iron selectivity decreased from 96272 to 534 for roasting pre-treatment and from 1.8 to 1 for alkali-roasting pre-treatment.

  14. A technical and economic assessment of fuel oil hydrotreating technology for steam power plant SO2 and NOx emissions control

    Directory of Open Access Journals (Sweden)

    peiman pourmoghaddam

    2016-12-01

    Full Text Available This work presents a simulation approach to the design and economic evaluation of fuel oil hydrotreating processes for the control of SO2 and NOx emission in an Iranian steam power plant. The percent of fuel oil desulphurization was estimated from the SO2 emissions standards for power plants. Based on two different scenarios according to (I European and (II Iranian standards, the design and simulation of hydrodesulphurization reactors, separation, heat recovery, and amine gas sweetening sections were performed and an economic assessment of the plant was investigated for each scenario. The results indicated the following: the cost price of each barrel of low sulfur fuel oil produced in such plants was estimated at  4.24 US$ for scenario (I and 3.17 US$ for scenario (II; the levelized cost of desulfurization in power production was estimated at 0.618 c/kWh for (I and 0.463 c/kWh for (II; and the social cost savings of replacing every barrel of low sulfur fuel oil instead of one barrel of high sulfur fuel oil were estimated at 26.7 US$ for (I and 13.6 US$ (II.

  15. The influence of the SO2ageing on the graffiti cleaning effectiveness with chemical procedures on a granite substrate.

    Science.gov (United States)

    Gomes, Vera; Dionísio, Amélia; Santiago Pozo-Antonio, J

    2018-06-01

    Graffiti are one of the most severe threats to Stone Cultural Heritage and are most of the times removed after long periods of environmental exposure. This research intends to evaluate the influence of the ageing of the graffitis on the effectiveness of their cleaning. So, comparative studies on unaged and on artificially SO 2 aged samples were conducted. Four graffiti spray colours were applied on a granite stone and cleaned with two chemical commercial cleaners: a solution of KOH and a solution of n-butyl acetate, xylene and alcohol isobutyl. The spray paints (unaged and aged) and cleaning effectiveness were characterized by stereomicroscopy, colour spectrophotometry, adhesion tests, SEM, μEDXRF, XRD and FTIR. The cleaning effectiveness was also evaluated through surface roughness and static contact angle measurements. The alkyd graffiti paints presented greatest resistance under SO 2 rich environments than the polyethylene paint. The aged polyethylene paint showed chemical modifications that resulted in graffiti losses and neo formed mineralogical phases in the surface of the paint. After ageing, the paints became more difficult to clean, showed higher global colour changes and higher residue percentages. No significant roughness variations were detected after chemical cleaning. After the cleaning procedures aged surfaces became more water repellent comparatively to unaged and reference samples. The best cleaning effectiveness was mainly achieved with the potassium hydroxide solution. Copyright © 2017 Elsevier B.V. All rights reserved.

  16. Impact of external industrial sources on the regional and local SO2 and O3 levels of the Mexico megacity

    Science.gov (United States)

    Almanza, V. H.; Molina, L. T.; Li, G.; Fast, J.; Sosa, G.

    2014-08-01

    The air quality of megacities can be influenced by external emission sources on both global and regional scales. At the same time their outflow emissions can exert an impact to the surrounding environment. The present study evaluates an SO2 peak observed on 24 March 2006 at the suburban supersite T1 and at ambient air quality monitoring stations located in the northern region of the Mexico City Metropolitan Area (MCMA) during the Megacity Initiative: Local and Global Research Observations (MILAGRO) field campaign. We found that this peak could be related to an important episodic emission event coming from Tizayuca region, northeast of the MCMA. Back-trajectory analyses suggest that the emission event started in the early morning at 04:00 LST and lasted for about 9 h. The estimated emission rate is about 2 kg s-1. To the best of our knowledge, sulfur dioxide emissions from the Tizayuca region have not been considered in previous studies. This finding suggests the possibility of "overlooked" emission sources in this region that could influence the air quality of the MCMA. This further motivated us to study the cement plants, including those in the state of Hidalgo and in the State of Mexico. It was found that they can contribute to the SO2 levels in the northeast (NE) region of the basin (about 42%), at the suburban supersite T1 (41%) and that at some monitoring stations their contribution can be even higher than the contribution from the Tula Industrial Complex (TIC). The contribution of the Tula Industrial Complex to regional ozone levels is estimated. The model suggests low contribution to the MCMA (1 to 4 ppb) and slightly higher contribution at the suburban T1 (6 ppb) and rural T2 (5 ppb) supersites. However, the contribution could be as high as 10 ppb in the upper northwest region of the basin and in the southwest and south-southeast regions of the state of Hidalgo. In addition, the results indicated that the ozone plume could also be transported to northwest

  17. Corrosion behavior of Fe3Al intermetallics with addition of lithium, cerium and nickel in 2.5 % SO2+N2 at 900 °C

    Directory of Open Access Journals (Sweden)

    González-Rodríguez, J. G.

    2012-12-01

    Full Text Available The corrosion behavior of Fe3Al-type intermetallic alloys with addition of 1 at. % cerium, lithium and nickel at high temperature has been studied. The various alloys were exposed to an environment composed of 2.5 % SO2+N2 at 900 °C for 48 h. For all the intermetallic tested, the corrosion kinetics showed a parabolic behavior. The alloy, which showed less corrosion rate, was the Fe3AlNi alloy, being Fe3AlCeLi the alloy with the highest corrosion rate. For the various alloys, energy dispersive X-ray spectroscopy analysis, EDS, on the developed scale only detected aluminum, oxygen, and traces of iron and cerium, suggesting the formation of alumina as main component. The intermetallic alloys showed oxide cracking and spalling. The intermetallic chemical composition played an important role in defining the oxide scale morphology and the extent of damage.Se estudió el comportamiento a la corrosión a alta temperatura de intermetálicos tipo Fe3Al con adición de 1at. % de cerio, litio y níquel. Las diferentes aleaciones fueron expuestas bajo un ambiente compuesto de 2,5 % SO2+N2 a 900 °C durante 48 h. Para todos los intermetálicos ensayados, la cinética de corrosión presentó un comportamiento parabólico. La aleación que mostró la menor velocidad de corrosión fue el intermetálico Fe3AlNi, siendo el intermetálico Fe3AlCeLi el de mayor velocidad de corrosión. Los análisis mediante espectroscopía de dispersión de rayos X, EDS, sobre la costra formada identificaron únicamente aluminio, oxígeno y trazas de hierro y cerio, lo que sugiere la formación de alúmina como el componente principal. Los intermetálicos mostraron agrietamiento y desprendimiento de la costra de óxido. La composición química de los intermetálicos tuvo un papel importante en la definición de la morfología del óxido formado y el grado de daño.

  18. Determination of the Rate Coefficients of the SO2 plus O plus M yields SO3 plus M Reaction

    Science.gov (United States)

    Hwang, S. M.; Cooke, J. A.; De Witt, K. J.; Rabinowitz, M. J.

    2010-01-01

    Rate coefficients of the title reaction R(sub 31) (SO2 +O+M yields SO3 +M) and R(sub 56) (SO2 + HO2 yields SO3 +OH), important in the conversion of S(IV) to S(VI),were obtained at T =970-1150 K and rho (sub ave) = 16.2 micro mol/cubic cm behind reflected shock waves by a perturbation method. Shock-heated H2/ O2/Ar mixtures were perturbed by adding small amounts of SO2 (1%, 2%, and 3%) and the OH temporal profiles were then measured using laser absorption spectroscopy. Reaction rate coefficients were elucidated by matching the characteristic reaction times acquired from the individual experimental absorption profiles via simultaneous optimization of k(sub 31) and k(sub 56) values in the reaction modeling (for satisfactory matches to the observed characteristic times, it was necessary to take into account R(sub 56)). In the experimental conditions of this study, R(sub 31) is in the low-pressure limit. The rate coefficient expressions fitted using the combined data of this study and the previous experimental results are k(sub 31,0)/[Ar] = 2.9 10(exp 35) T(exp ?6.0) exp(?4780 K/T ) + 6.1 10(exp 24) T(exp ?3.0) exp(?1980 K/T ) cm(sup 6) mol(exp ?2)/ s at T = 300-2500 K; k(sub 56) = 1.36 10(exp 11) exp(?3420 K/T ) cm(exp 3)/mol/s at T = 970-1150 K. Computer simulations of typical aircraft engine environments, using the reaction mechanism with the above k(sub 31,0) and k(sub 56) expressions, gave the maximum S(IV) to S(VI) conversion yield of ca. 3.5% and 2.5% for the constant density and constant pressure flow condition, respectively. Moreover, maximum conversions occur at rather higher temperatures (?1200 K) than that where the maximum k(sub 31,0) value is located (approximately 800 K). This is because the conversion yield is dependent upon not only the k(sup 31,0) and k(sup 56) values (production flux) but also the availability of H, O, and HO2 in the system (consumption flux).

  19. A theoretical investigation of gaseous absorption by water droplets from SO2-HNO3-NH3-CO2-HCl mixtures

    Science.gov (United States)

    Adewuyi, Y. G.; Carmichael, G. R.

    1982-01-01

    A physical-chemical model is developed and used to investigate gaseous absorption by water droplets from trace gas mixtures. The model is an extension of that of Carmichael and Peters (1979) and includes the simultaneous absorption of SO2, NH3, HNO3, CO2, and HCl. Gas phase depletion is also considered. Presented results demonstrate that the absorption behavior of raindrops is strongly dependent on drop size, fall distance, trace gas concentrations, and the chemical and physical properties of the constituents of the mixture. In addition, when gas phase depletion is considered, the absorption rates and equilibrium values are also dependent on the precipitation rate itself. Also, the trace constituents liquid phase concentrations may be a factor of six or more lower when gas depletion is considered then when the depletion is ignored. However, the hydrogen ion concentration may be insensitive to the gas phase depletion.

  20. Federal NOx Budget Trading Program and CAIR NOx and SO2 Trading Programs (40 CFR Part 97)

    Science.gov (United States)

    This part establishes general provisions and the applicability, permitting, allowance, excess emissions, monitoring, and opt-in provisions for the federal NOx Budget Trading Program as a means of mitigating interstate transport of ozone and nitrogen oxides

  1. Adsorption behavior of Co anchored on graphene sheets toward NO, SO2, NH3, CO and HCN molecules

    International Nuclear Information System (INIS)

    Tang, Yanan; Chen, Weiguang; Li, Chenggang; Pan, Lijun; Dai, Xianqi; Ma, Dongwei

    2015-01-01

    Graphical abstract: - Highlights: • In contrast to the pristine graphene, a vacancy defect in graphene strongly stabilizes the Co atom. • The positively charged of Co atom on graphene can regulate the stability of gas molecules. • Different gas molecules can modulate the electronic structure of Co–graphene systems. • The adsorbed NO on Co–graphene can effectively regulate the magnetic properties of systems. - Abstract: Based on the first-principles of density-functional theory (DFT), the effects of gas adsorption on the change in geometric stability, electronic structure and magnetic properties of graphene with anchored Co (Co–graphene) systems were investigated. A single Co adatom interacts much weaker with pristine graphene (Co/pri–graphene) than with the graphene containing a single vacancy (Co/SV–graphene). The Co dopant provides more electrons to the dangling bonds of carbon atom at defective site and exhibits more positive charges, which makes Co/SV–graphene less prone to be adsorbed by gas molecules in comparison to Co/pri–graphene. It is found that the electronic structure and magnetic properties of Co–graphene systems can be modulated by adsorbing gas molecules. Except the NH 3 molecule, the adsorbed NO, SO 2 , CO or HCN as electron acceptors on the Co/pri–graphene can exhibit semiconducting properties. Among the gas molecules, the strong adsorption of NO molecule can effectively regulate the magnetic properties of Co–graphene systems. Moreover, the stable configuration of Co/SV–graphene is more likely to be the gas sensor for detecting NO and SO 2 . The results validate that the reactivity of atomic-scale catalyst is supported on graphene sheets, which is expected to be potentially efficient in the gas sensors and electronic device

  2. Molten V2O5/Cs0.9K0.9Na0.2S2O7 and V2O5/K2S2O7 catalysts as electrolytes in an electrocatalytic membrane separation device for SO2 removal

    DEFF Research Database (Denmark)

    Rasmussen, Søren Birk; Eriksen, Kim Michael; Fehrmann, Rasmus

    2002-01-01

    Bench scale fuel cell tests have been carried out on the SO2 oxidation catalyst systems V2O5/M2S2O7 (M = alkali) used as electrolytes in a standard molten carbonate fuel cell (MCFC) fuel cell setup for removal of SO2 from power plant flue gases. Porous LixNi(1-x)O electrodes were used both as anode...

  3. Highly sensitive and selective SO2 MOF sensor: the integration of MFM-300 MOF as a sensitive layer on a capacitive interdigitated electrode

    KAUST Repository

    Chernikova, Valeriya

    2018-03-05

    We report on the fabrication of an advanced chemical capacitive sensor for the detection of sulfur dioxide (SO2) at room temperature. The sensing layer based on an indium metal–organic framework (MOF), namely MFM-300, is coated solvothermally on a functionalized capacitive interdigitated electrode. The fabricated sensor exhibits significant detection sensitivity to SO2 at concentrations down to 75 ppb, with the lower detection limit estimated to be around 5 ppb. The MFM-300 MOF sensor demonstrates highly desirable detection selectivity towards SO2 vs. CH4, CO2, NO2 and H2, as well as an outstanding SO2 sensing stability.

  4. OMS, OM(η2-SO), and OM(η2-SO)(η2-SO2) molecules (M = Ti, Zr, Hf): infrared spectra and density functional calculations.

    Science.gov (United States)

    Liu, Xing; Wang, Xuefeng; Wang, Qiang; Andrews, Lester

    2012-07-02

    Infrared spectra of the matrix isolated OMS, OM(η(2)-SO), and OM(η(2)-SO)(η(2)-SO(2)) (M = Ti, Zr, Hf) molecules were observed following laser-ablated metal atom reactions with SO(2) during condensation in solid argon and neon. The assignments for the major vibrational modes were confirmed by appropriate S(18)O(2) and (34)SO(2) isotopic shifts, and density functional vibrational frequency calculations (B3LYP and BPW91). Bonding in the initial OM(η(2)-SO) reaction products and in the OM(η(2)-SO)(η(2)-SO(2)) adduct molecules with unusual chiral structures is discussed.

  5. Reaction characteristics of Ca(OH)2, HCl and SO2 at low temperature in a spray dryer integrated with a fabric filter.

    Science.gov (United States)

    Liu, Zhen-Shu; Wey, Ming-Yen; Lin, Chiou-Liang

    2002-12-02

    The objective of this research was to evaluate the reaction characteristics of CaOH2, HCl and SO2 in the flue gas emitted by a laboratory incinerator. The amount of sulfur retained in the residues (including the spray dryer ash and baghouse ash) was also evaluated in this study. The experimental parameters included HCl concentration (500-2000 ppm), SO2 concentration (500-2000 ppm), relative humidity (40-80% RH), and the addition of CaCl2 (30 wt.%). The results indicated that an HCl concentration of 500-2000 ppm did not affect HCl removal efficiency in the spray dryer at 150 degrees C and 45+/-5% RH. On the other hand, increase in SO2 concentration from 500 to 2000 ppm enhanced SO2 removal at 150 degrees C and 75+/-5% RH. Moreover, increase in removal efficiency of SO2 was more obvious when the relative humidity was greater than 80%. When the flue gas contained both HCl and SO2 simultaneously, the removal efficiency of SO2 could increase from 56.7 to 90.33% at HCl concentration of 236 ppm. However, when the concentration of HCl exceeded 535 ppm, the removal efficiency of SO2 decreased with increasing concentration of HCl. The removal efficiency of SO2 could be increase to 97.7% with the addition of CaCl2.

  6. Highly-stable and -flexible graphene/(CF3SO2)2NH/graphene transparent conductive electrodes for organic solar cells

    Science.gov (United States)

    Seo, Sang Woo; Lee, Ha Seung; Shin, Dong Hee; Kim, Ju Hwan; Jang, Chan Wook; Kim, Jong Min; Kim, Sung; Choi, Suk-Ho

    2017-10-01

    We first employ highly-stable and -flexible (CF3SO2)2NH-doped graphene (TFSA/GR) and GR-encapsulated TFSA/GR (GR/TFSA/GR) transparent conductive electrodes (TCEs) prepared on polyethylene terephthalate substrates for flexible organic solar cells (OSCs). Compared to conventional indium tin oxide (ITO) TCEs, the TFSA-doped-GR TCEs show higher optical transmittance and larger sheet resistance. The TFSA/GR and GR/TFSA/GR TCEs show work functions of 4.89 ± 0.16 and 4.97 ± 0.18 eV, respectively, which are not only larger than those of the ITO TCEs but also indicate p-type doping of GR, and are therefore more suitable for anode TCEs of OSCs. In addition, typical GR/TFSA/GR-TCE OSCs are much more mechanically flexible than the ITO-TCE ones with their photovoltaic parameters being similar, as proved by bending tests as functions of cycle and curvature.

  7. Security, privacy and trust in cloud systems

    CERN Document Server

    Nepal, Surya

    2013-01-01

    The book compiles technologies for enhancing and provisioning security, privacy and trust in cloud systems based on Quality of Service requirements. It is a timely contribution to a field that is gaining considerable research interest, momentum, and provides a comprehensive coverage of technologies related to cloud security, privacy and trust. In particular, the book includes - Cloud security fundamentals and related technologies to-date, with a comprehensive coverage of evolution, current landscape, and future roadmap. - A smooth organization with introductory, advanced and specialist content

  8. Current and future trends in cloud CRM

    OpenAIRE

    Nemček, Sebastian

    2011-01-01

    The diploma thesis is committed to mapping CRM applications available in cloud and trends within. The goal is to describe what CRM is, how it evolved into Cloud CRM, analyze main differences between the two approaches and analyze trends that can be observed in CRM market and CRM applications. This is coupled with description of the most common CRM solutions and products available both on-premises as well as on-demand. In the first part, the thesis introduces theory behind Customer Relationshi...

  9. Increased incidence of allergic rhinitis, bronchitis and asthma, in children living near a petrochemical complex with SO2pollution.

    Science.gov (United States)

    Chiang, Tzu-Ying; Yuan, Tzu-Hsuen; Shie, Ruei-Hao; Chen, Chen-Fang; Chan, Chang-Chuan

    2016-11-01

    This study aims to investigate incidence of allergic rhinitis, bronchitis and asthma, in children living near a petrochemical complex with SO 2 pollution obtained by air monitoring stations. A total of 587 children aged 11 to 14 were recruited and classified into high and low exposure groups based on a radius of 10km from the complex. To study the influence of health on children since the operation of complex in 1999 and observe the difference of these diseases' short-term and long-term impact, we obtained the incidence rates of allergic rhinitis (ICD-9: 477), bronchitis (490-491) and asthma (493) from the Taiwan Health Insurance Database for three periods: 1999-2002, 1999-2006, and 1999-2010. Since 2001, the mean and 99th percentile of SO 2 concentrations in the high exposure area have been significantly higher than those in low exposure area. There were significant differences between the high and low exposure groups in the percentage of smoking, alcohol consumption, passive smoking exposure and incense burning habits. The incidence rates of three intervals were 26.9%, 35.7%, 41.7%; 8.3%, 8.8%, 10.2%; 18.5%, 25.0%, 26.9% for allergic rhinitis, bronchitis and asthma in high exposure group. Significant differences were found between groups for allergic rhinitis in all periods, bronchitis in the first two periods, and asthma in the first period using Student's t-test. After we adjusted age, gender, group, living near roads, incense burning and passive smoking exposure, the hazard ratios between exposure groups were 3.05, 2.74, and 1.93 for allergic rhinitis with significant difference in three periods, and 2.53, 1.92 and 1.72 for bronchitis with significant difference in first period and 1.60, 1.28 and 1.29 for asthma with significant difference in first period by Cox regression. The higher incidence of allergic rhinitis was related to boys and living near roads and the higher incidence of asthma was also related to younger children, boys, and passive smoking

  10. Detection of SO2, HCl and CO2 in Arenal Volcano Eruptive Plume Using MASTER Multispectral Images

    Science.gov (United States)

    Bonatti, J.; Berrocal, M.; Malavassi, E.

    2004-12-01

    The Costa Rica Airborne Research and Technology Applications (CARTA) Mission developed in March-April, 2003 was a join effort between the National Program for Airtransported Missions of the National Center for High Technology of Costa Rica formed by the four public universities in Costa Rica, and NASA. This mission took aerial infrared photography and multiespectral images using the MASTER sensor of 70% of the national territory of Costa Rica. Multiespectral images were taken from Arenal volcano at high (13780 m) and at low (3450 m) altitude. The MASTER images have an aperture ranging between 0.44 micrometers in the visible and 13 micrometers in the thermic infrared. In addition, the distribution of the 50 channels of the MASTER sensor, have been arranged to avoid the influence of water vapor, always present in large quantities in the atmosphere and also in volcanic gases. We determined that SO2 is clearly visible between 8.5-9.3 micrometers (LWIR), and CO2, H2S and HCl in a smaller bandwidth 3.5-4.4 micrometers (MWIR). Another gas detected at Arenal volcanic plumes is methane, in a bandwidth between 7.7-8.1 micrometers (LWIR). When both multispectral images were taken, Arenal volcano had an active lava flow descending its NE flank and no significative winds were blowing, so the eruptive plume was rising almost vertically from the active vent. Profiles of gas concentration collected from the above mentioned bands were performed on the image using the software ENVI to detect different species present in volcanic gases. The concentration of volcanic gases in the multiespectral image was largest above the active crater (north vent of Crater C), and lower on the short active lava flow whose blocks were cascading down up to 1 km on the NE flank. Significant amounts of SO2 were measured above the lava flow and the fan of cascading blocks suggesting that the cooling lava continues to release magmatic gases as their cascading blocks move down flank of the volcano. The

  11. Pre-hospital portable monitoring of cerebral regional oxygen saturation (rSO2) in seven patients with out-of-hospital cardiac arrest.

    Science.gov (United States)

    Hirose, Tomoya; Shiozaki, Tadahiko; Nomura, Junji; Hamada, Yasuto; Sato, Keiichi; Katsura, Kazuya; Ehara, Naoki; Wakai, Akinori; Shimizu, Kentaro; Ohnishi, Mitsuo; Hayashida, Sumito; Sadamitsu, Daikai; Shimazu, Takeshi

    2016-08-31

    In recent years, measurement of cerebral regional oxygen saturation (rSO2) has attracted attention during resuscitation. However, serial changes of cerebral rSO2 in pre-hospital settings are unclear. The objective of this study was to clarify serial changes in cerebral rSO2 of patients with out-of-hospital cardiac arrest (OHCA) in the pre-hospital setting. We recently developed a portable rSO2 monitor that is small (170 × 100 × 50 mm in size and 600 g in weight) enough to carry in pre-hospital settings. The sensor is attached to the patient's forehead by the ELT (Emergency Life-saving Technician), and it monitors rSO2 continuously. From June 2013 through August 2014, serial changes in cerebral rSO2 in seven patients were evaluated. According to the results of the serial changes in rSO2, four patterns of rSO2 change were found, as follows. Type 1: High rSO2 (around about 60 %) type (n = 1). Initial electrocardiogram was ventricular fibrillation and ROSC (return of spontaneous circulation) could be diagnosed in pre-hospital setting. Her outcome at discharge was Good Recovery (GR). Type 2: Low rSO2 (around about 45-50 %) type (n = 3). They did not get ROSC even once. Type 3: Gradually decreasing rSO2 type (n = 2): ROSC could be diagnosed in hospital, but not in pre-hospital setting. Their outcomes at discharge were not GR. Type 4: other type (n = 1). In this patient with ROSC when ELT started cerebral rSO2 measurement, cerebral rSO2 was 67.3 % at measurement start, it dropped gradually to 54.5 %, and then rose to 74.3 %. The cerebral oxygenation was impaired due to possible cardiac arrest again, and after that, ROSC led to the recovery of cerebral blood flow. We could measure serial changes in cerebral rSO2 in seven patients with OHCA in the pre-hospital setting. Our data suggest that pre-hospital monitoring of cerebral rSO2 might lead to a new resuscitation strategy.

  12. SU-E-T-326: The Oxygen Saturation (SO2) and Breath-Holding Time Variation Applied Active Breathing Control (ABC)

    Energy Technology Data Exchange (ETDEWEB)

    Gong, G; Yin, Y [Shandong Cancer Hospital, Jinan, Shandong (China)

    2014-06-01

    Purpose: To study the oxygen saturation (SO2) and breath-holding time variation applied active breathing control (ABC) in radiotherapy of tumor. Methods: 24 volunteers were involved in our trials, and they all did breath-holding motion assisted by ELEKTA Active Breathing Coordinator 2.0 for 10 times respectively. And the patient monitor was used to observe the oxygen saturation (SO2) variation. The variation of SO2, and length of breath-holding time and the time for recovering to the initial value of SO2 were recorded and analyzed. Results: (1) The volunteers were divided into two groups according to the SO2 variation in breath-holding: A group, 14 cases whose SO2 reduction were more than 2% (initial value was 97% to 99%, while termination value was 91% to 96%); B group, 10 cases were less than 2% in breath-holding without inhaling oxygen. (2) The interfraction breath holding time varied from 8 to 20s for A group compared to the first breath-holding time, and for B group varied from 4 to 14s. (3) The breathing holding time of B group prolonged mean 8s, compared to A group. (4) The time for restoring to the initial value of SO2 was from 10s to 30s. And the breath-holding time shortened obviously for patients whose SO2 did not recover to normal. Conclusion: It is very obvious that the SO2 reduction in breath-holding associated with ABC for partial people. It is necessary to check the SO2 variation in breath training, and enough time should be given to recover SO2.

  13. Sulfate Formation Enhanced by a Cocktail of High NOx, SO2, Particulate Matter, and Droplet pH during Haze-Fog Events in Megacities in China: An Observation-Based Modeling Investigation.

    Science.gov (United States)

    Xue, Jian; Yuan, Zibing; Griffith, Stephen M; Yu, Xin; Lau, Alexis K H; Yu, Jian Zhen

    2016-07-19

    In recent years in a few Chinese megacities, fog events lasting one to a few days have been frequently associated with high levels of aerosol loading characterized by high sulfate (as high as 30 μg m(-3)), therefore termed as haze-fog events. The concomitant pollution characteristics include high gas-phase mixing ratios of SO2 (up to 71 ppbv) and NO2 (up to 69 ppbv), high aqueous phase pH (5-6), and smaller fog droplets (as low as 2 μm), resulting from intense emissions from fossil fuel combustion and construction activities supplying abundant Ca(2+). In this work, we use an observation-based model for secondary inorganic aerosols (OBM-SIA) to simulate sulfate formation pathways under conditions of haze-fog events encountered in Chinese megacities. The OBM analysis has identified, at a typical haze-fogwater pH of 5.6, the most important pathway to be oxidation of S(IV) by dissolved NO2, followed by the heterogeneous reaction of SO2 on the aerosol surface. The aqueous phase oxidation of S(IV) by H2O2 is a very minor formation pathway as a result of the high NOx conditions suppressing H2O2 formation. The model results indicate that the unique cocktail of high fogwater pH, high concentrations of NO2, SO2, and PM, and small fog droplets are capable of greatly enhancing sulfate formation. Such haze-fog conditions could lead to rapid sulfate production at night and subsequently high PM2.5 in the morning when the fog evaporates. Sulfate formation is simulated to be highly sensitive to fogwater pH, PM, and precursor gases NO2 and SO2. Such insights on major contributing factors imply that reduction of road dust and NOx emissions could lessen PM2.5 loadings in Chinese megacities during fog events.

  14. Initiation of secondary ice production in clouds

    Science.gov (United States)

    Sullivan, Sylvia C.; Hoose, Corinna; Kiselev, Alexei; Leisner, Thomas; Nenes, Athanasios

    2018-02-01

    Disparities between the measured concentrations of ice-nucleating particles (INPs) and in-cloud ice crystal number concentrations (ICNCs) have led to the hypothesis that mechanisms other than primary nucleation form ice in the atmosphere. Here, we model three of these secondary production mechanisms - rime splintering, frozen droplet shattering, and ice-ice collisional breakup - with a six-hydrometeor-class parcel model. We perform three sets of simulations to understand temporal evolution of ice hydrometeor number (Nice), thermodynamic limitations, and the impact of parametric uncertainty when secondary production is active. Output is assessed in terms of the number of primarily nucleated ice crystals that must exist before secondary production initiates (NINP(lim)) as well as the ICNC enhancement from secondary production and the timing of a 100-fold enhancement. Nice evolution can be understood in terms of collision-based nonlinearity and the phasedness of the process, i.e., whether it involves ice hydrometeors, liquid ones, or both. Ice-ice collisional breakup is the only process for which a meaningful NINP(lim) exists (0.002 up to 0.15 L-1). For droplet shattering and rime splintering, a warm enough cloud base temperature and modest updraft are the more important criteria for initiation. The low values of NINP(lim) here suggest that, under appropriate thermodynamic conditions for secondary ice production, perturbations in cloud concentration nuclei concentrations are more influential in mixed-phase partitioning than those in INP concentrations.

  15. Modeling global persistent organic chemicals in clouds

    Science.gov (United States)

    Mao, Xiaoxuan; Gao, Hong; Huang, Tao; Zhang, Lisheng; Ma, Jianmin

    2014-10-01

    A cloud model was implemented in a global atmospheric transport model to simulate cloud liquid water content and quantify the influence of clouds on gas/aqueous phase partitioning of persistent organic chemicals (POCs). Partitioning fractions of gas/aqueous and particle phases in clouds for three POCs α-hexachlorocyclohexane (α-HCH), polychlorinated biphenyl-28 (PCB-28), and PCB-138 in a cloudy atmosphere were estimated. Results show that the partition fraction of these selected chemicals depend on cloud liquid water content (LWC) and air temperature. We calculated global distribution of water droplet/ice particle-air partitioning coefficients of the three chemicals in clouds. The partition fractions at selected model grids in the Northern Hemisphere show that α-HCH, a hydrophilic chemical, is sorbed strongly onto cloud water droplets. The computed partition fractions at four selected model grids show that α-HCH tends to be sorbed onto clouds over land (source region) from summer to early fall, and over ocean from late spring to early fall. 20-60% of α-HCH is able to be sorbed to cloud waters over mid-latitude oceans during summer days. PCB-138, one of hydrophobic POCs, on the other hand, tends to be sorbed to particles in the atmosphere subject to air temperature. We also show that, on seasonal or annual average, 10-20% of averaged PCB-28 over the Northern Hemisphere could be sorbed onto clouds, leading to reduction of its gas-phase concentration in the atmosphere.

  16. Global simulations of aerosol processing in clouds

    Directory of Open Access Journals (Sweden)

    C. Hoose

    2008-12-01

    Full Text Available An explicit and detailed representation of in-droplet and in-crystal aerosol particles in stratiform clouds has been introduced in the global aerosol-climate model ECHAM5-HAM. The new scheme allows an evaluation of the cloud cycling of aerosols and an estimation of the relative contributions of nucleation and collision scavenging, as opposed to evaporation of hydrometeors in the global aerosol processing by clouds. On average an aerosol particle is cycled through stratiform clouds 0.5 times. The new scheme leads to important changes in the simulated fraction of aerosol scavenged in clouds, and consequently in the aerosol wet deposition. In general, less aerosol is scavenged into clouds with the new prognostic treatment than what is prescribed in standard ECHAM5-HAM. Aerosol concentrations, size distributions, scavenged fractions and cloud droplet concentrations are evaluated and compared to different observations. While the scavenged fraction and the aerosol number concentrations in the marine boundary layer are well represented in the new model, aerosol optical thickness, cloud droplet number concentrations in the marine boundary layer and the aerosol volume in the accumulation and coarse modes over the oceans are overestimated. Sensitivity studies suggest that a better representation of below-cloud scavenging, higher in-cloud collision coefficients, or a reduced water uptake by seasalt aerosols could reduce these biases.

  17. A methodology for the economic assessment of material damage caused by SO2 and NOx emissions in Europe

    International Nuclear Information System (INIS)

    Mayerhofer, P.; Weltschev, M.; Trukenmueller, A.; Friedrich, R.

    1995-01-01

    Damage to materials causes high economic losses in Europe. A large part of this damage can be attributed to the emissions caused by the energy and the transport sector. In the paper, the procedure for the economic assessment of material damages caused by SO 2 and NO x emissions in Europe is described. Model and data requirements are outlined, and gaps and uncertainties of the quantification are discussed. Two types of results are presented. First, the marginal (additional) costs of damage to material caused by an additional power plant are assessed. The analysis covers plants with different technologies. Results for the fossil power plants are in the range of 0.0062 to 0.12 mECU/kWh. In addition, the total economic material damage due to the present air pollution was assessed. It is in the range of 2.9 to 5.3 x 10 9 ECU/year. However, the analysis has many uncertainties. Most noteworthy are the material inventories and partially the damage functions and input data. 15 refs., 1 fig., 1 tab

  18. Emissions of Volatile Inorganic Halogens, Carboxylic Acids, NH3, and SO2 From Experimental Burns of Southern African Biofuels

    Science.gov (United States)

    Keene, W. C.; Lobert, J. M.; Lobert, J. M.; Maben, J. R.; Scharffe, D. H.; Crutzen, P. J.; Crutzen, P. J.

    2001-12-01

    As part of SAFARI 2000, biofuels (savanna grasses, shrubs, woody plants, litter, agricultural waste, and charcoal) were sampled during late summer and early autumn in the savannah of Kruger National Park, the Kalahari of Etosha National Park, and the Miombo woodlands in Zambia and Malawi. Sixty subsamples were experimentally burned under semi-controlled conditions at the Max Planck Institute for Chemistry in Mainz, Germany. Emissions were sampled with tandem mist chambers to quantify HCl, CH3COOH, HCOOH, NH3, and SO2 and with a high-volume filter pack to quantify volatile inorganic Cl, Br, and I. The elemental compositions of the fuel and ash from each burn were also analyzed. Molar emission ratios of these species relative to CO, CO2, and the elemental composition of the fuel will be calculated and used to estimate regional emissions from biomass burning over southern Africa. The relative contributions of each species to elemental mass balances during burns will also be assessed. >http://jurgenlobert.org/projects/mpi_safari/ and

  19. Heterogeneous reaction of SO2 with soot: The roles of relative humidity and surface composition of soot in surface sulfate formation

    Science.gov (United States)

    Zhao, Yan; Liu, Yongchun; Ma, Jinzhu; Ma, Qingxin; He, Hong

    2017-03-01

    The conversion of SO2 to sulfates on the surface of soot is still poorly understood. Soot samples with different fractions of unsaturated hydrocarbons and oxygen-containing groups were prepared by combusting n-hexane under well-controlled conditions. The heterogeneous reaction of SO2 with soot was investigated using in situ attenuated total internal reflection infrared (ATR-IR) spectroscopy, ion chromatography (IC) and a flow tube reactor at the ambient pressure and relative humidity (RH). Water promoted SO2 adsorption and sulfate formation at the RH range from 6% to 70%, while exceeded water condensed on soot was unfavorable for sulfate formation due to inhibition of SO2 adsorption when RH was higher than 80%. The surface composition of soot, which was governed by combustion conditions, also played an important role in the heterogeneous reaction of SO2 with soot. This effect was found to greatly depend on RH. At low RH of 6%, soot with the highest fuel/oxygen ratio of 0.162 exhibited a maximum uptake capacity for SO2 because it contained a large amount of aromatic Csbnd H groups, which acted as active sites for SO2 adsorption. At RH of 54%, soot produced with a fuel/oxygen ratio of 0.134 showed the highest reactivity toward SO2 because it contained appropriate amounts of aromatic Csbnd H groups and oxygen-containing groups, subsequently leading to the optimal surface concentrations of both SO2 and water. These results suggest that variation in the surface composition of soot from different sources and/or resulting from chemical aging in the atmosphere likely affects the conversion of SO2 to sulfates.

  20. The operational eEMEP model version 10.4 for volcanic SO2 and ash forecasting

    Science.gov (United States)

    Steensen, Birthe M.; Schulz, Michael; Wind, Peter; Valdebenito, Álvaro M.; Fagerli, Hilde

    2017-05-01

    This paper presents a new version of the EMEP MSC-W model called eEMEP developed for transportation and dispersion of volcanic emissions, both gases and ash. EMEP MSC-W is usually applied to study problems with air pollution and aerosol transport and requires some adaptation to treat volcanic eruption sources and effluent dispersion. The operational set-up of model simulations in case of a volcanic eruption is described. Important choices have to be made to achieve CPU efficiency so that emergency situations can be tackled in time, answering relevant questions of ash advisory authorities. An efficient model needs to balance the complexity of the model and resolution. We have investigated here a meteorological uncertainty component of the volcanic cloud forecast by using a consistent ensemble meteorological dataset (GLAMEPS forecast) at three resolutions for the case of SO2 emissions from the 2014 Barðarbunga eruption. The low resolution (40 × 40 km) ensemble members show larger agreement in plume position and intensity, suggesting that the ensemble here does not give much added value. To compare the dispersion at different resolutions, we compute the area where the column load of the volcanic tracer, here SO2, is above a certain threshold, varied for testing purposes between 0.25 and 50 Dobson units. The increased numerical diffusion causes a larger area (+34 %) to be covered by the volcanic tracer in the low resolution simulations than in the high resolution ones. The higher resolution (10 × 10 km) ensemble members show higher column loads farther away from the volcanic eruption site in narrower clouds. Cloud positions are more varied between the high resolution members, and the cloud forms resemble the observed clouds more than the low resolution ones. For a volcanic emergency case this means that to obtain quickly results of the transport of volcanic emissions, an individual simulation with our low resolution is sufficient; however, to forecast peak

  1. Evaluation of the SO2 and NOx offset ratio method to account for secondary PM2.5 formation.

    Science.gov (United States)

    Guerra, Sergio A; Olsen, Shannon R; Anderson, Jared J

    2014-03-01

    The U.S. Environmental Protection Agency (EPA), state and local agencies have focused their efforts in assessing secondary fine particulate matter (aerodynamic diameter Pollution Control Agency (MPCA) have developed area-specific offset ratios for SO2 and NOx based on Comprehensive Air Quality Model with Extensions (CAMx) evaluations for air dispersion modeling analyses. The current study evaluates the effect on American Meteorological Society/Environmental Protection Agency Regulatory Model (AERMOD) predicted concentrations from the use of EPA and MPCA developed ratios. The study assesses the effect of these ratios on an electric generating utility (EGU), taconite mine, food processing plant, and a pulp and paper mill. The inputs used for these four scenarios are based on common stack parameters and emissions based on available data. The effect of background concentrations also evaluates these scenarios by presenting results based on uniform annual PM2.5 background values. This evaluation study helps assess the viability of the offset ratio method developed by NACAA in estimating primary and secondary PM2.5 concentrations. An alternative Tier 2 approach to combine modeled and monitored concentrations is also presented. On January 4, 2012, the EPA committed to engage in rulemaking to evaluate updates to the Guideline on Air Quality Models (Appendix W of 40 CFR 51) and, as appropriate, incorporate new analytical techniques or models for secondary PM2.5. As a result, the National Association of Clean Air Agencies (NACAA) developed a screening method involving offset ratios to account for secondary PM2.5 formation. The use of this method is promising to evaluate total (direct and indirect) PM2.5 impacts for permitting purposes. Therefore, the evaluation of this method is important to determine its viability for widespread use.

  2. The (2'S,7'S)-O-(2-methylbutanoyl)-columbianetin as a novel allergic rhinitis-control agent.

    Science.gov (United States)

    Nam, Sun-Young; Kim, Min-Ho; Seo, Youngwan; Choi, Youngjin; Jang, Jae-Bum; Kang, In-Cheol; Kim, Myong-Jo; Pak, Sok Cheon; Kim, Hyung-Min; Jeong, Hyun-Ja

    2014-03-11

    The (2'S,7'S)-O-(2-methylbutanoyl)-columbianetin (OMC) is a novel secondary metabolite extracted from Corydalis heterocarpa, which has long been used as a folk medicine for various inflammatory diseases in Korea. We examined the effect of OMC on allergic rhinitis (AR). We assessed the therapeutic effects and regulatory mechanisms of OMC on the phorbol 12-myristate 13-acetate plus A23187-stimulated mast cell line, HMC-1 cells and ovalbumin (OVA)-induced AR models. OMC significantly decreased the releases of histamine and tryptase from stimulated HMC-1 cells. The degranulation process, characterized by morphological extension of the filopodia on the surface and membrane ruffling, was strongly induced in the stimulated-HMC-1 cell, however OMC suppressed the morphological changes in stimulated-HMC-1 cells. OMC reduced the production and mRNA expression of inflammatory cytokines. These inhibitory actions by OMC were dependent on the regulation of mitogen-activated protein kinases, nuclear factor-κB, and caspapase-1 signaling pathways. In the AR animal model, the increased rub scores and AR biomarkers (histamine and IgE) in ovalbumin (OVA)-sensitized mice were significantly reduced by the administration of OMC. Furthermore, eosinophils and mast cell infiltrations in nasal mucosa tissue were also blocked through the regulation of macrophage-inflammatory protein and intercellular adhesion molecule-1 levels. OMC showed the possibility to regulate AR in activated mast cells and OVA-induced AR models. Hence, we suggest that OMC is a powerful and feasible new agent to suppress AR. Copyright © 2014 Elsevier Inc. All rights reserved.

  3. Validation Studies of the Accuracy of Various SO2 Gas Retrievals in the Thermal InfraRed (8-14 μm)

    Science.gov (United States)

    Gabrieli, A.; Wright, R.; Lucey, P. G.; Porter, J. N.; Honniball, C.; Garbeil, H.; Wood, M.

    2016-12-01

    Quantifying hazardous SO2 in the atmosphere and in volcanic plumes is important for public health and volcanic eruption prediction. Remote sensing measurements of spectral radiance of plumes contain information on the abundance of SO2. However, in order to convert such measurements into SO2 path-concentrations, reliable inversion algorithms are needed. Various techniques can be employed to derive SO2 path-concentrations. The first approach employs a Partial Least Square Regression model trained using MODTRAN5 simulations for a variety of plume and atmospheric conditions. Radiances at many spectral wavelengths (8-14 μm) were used in the algorithm. The second algorithm uses measurements inside and outside the SO2 plume. Measurements in the plume-free region (background sky) make it possible to remove background atmospheric conditions and any instrumental effects. After atmospheric and instrumental effects are removed, MODTRAN5 is used to fit the SO2 spectral feature and obtain SO2 path-concentrations. The two inversion algorithms described above can be compared with the inversion algorithm for SO2 retrievals developed by Prata and Bernardo (2014). Their approach employs three wavelengths to characterize the plume temperature, the atmospheric background, and the SO2 path-concentration. The accuracy of these various techniques requires further investigation in terms of the effects of different atmospheric background conditions. Validating these inversion algorithms is challenging because ground truth measurements are very difficult. However, if the three separate inversion algorithms provide similar SO2 path-concentrations for actual measurements with various background conditions, then this increases confidence in the results. Measurements of sky radiance when looking through SO2 filled gas cells were collected with a Thermal Hyperspectral Imager (THI) under various atmospheric background conditions. These data were processed using the three inversion approaches

  4. DATA SECURITY ISSUES IN CLOUD COMPUTING: REVIEW

    Directory of Open Access Journals (Sweden)

    Hussam Alddin Shihab Ahmed

    2016-02-01

    Full Text Available Cloud computing is an internet based model that empower on demand ease of access and pay for the usage of each access to shared pool of networks. It is yet another innovation that fulfills a client's necessity for computing resources like systems, stockpiling, servers, administrations and applications. Securing the Data is considered one of the principle significant challenges and concerns for cloud computing. This persistent problem is getting more affective due to the changes in improving cloud computing technology. From the perspective of the Clients, cloud computing is a security hazard especially when it comes to assurance affirmation issues and data security, remain the most basically which backs off for appropriation of Cloud Computing administrations. This paper audits and breaks down the essential issue of cloud computing and depicts the information security and protection of privacy issues in cloud.

  5. Initiation of secondary ice production in clouds

    Directory of Open Access Journals (Sweden)

    S. C. Sullivan

    2018-02-01

    Full Text Available Disparities between the measured concentrations of ice-nucleating particles (INPs and in-cloud ice crystal number concentrations (ICNCs have led to the hypothesis that mechanisms other than primary nucleation form ice in the atmosphere. Here, we model three of these secondary production mechanisms – rime splintering, frozen droplet shattering, and ice–ice collisional breakup – with a six-hydrometeor-class parcel model. We perform three sets of simulations to understand temporal evolution of ice hydrometeor number (Nice, thermodynamic limitations, and the impact of parametric uncertainty when secondary production is active. Output is assessed in terms of the number of primarily nucleated ice crystals that must exist before secondary production initiates (NINP(lim as well as the ICNC enhancement from secondary production and the timing of a 100-fold enhancement. Nice evolution can be understood in terms of collision-based nonlinearity and the phasedness of the process, i.e., whether it involves ice hydrometeors, liquid ones, or both. Ice–ice collisional breakup is the only process for which a meaningful NINP(lim exists (0.002 up to 0.15 L−1. For droplet shattering and rime splintering, a warm enough cloud base temperature and modest updraft are the more important criteria for initiation. The low values of NINP(lim here suggest that, under appropriate thermodynamic conditions for secondary ice production, perturbations in cloud concentration nuclei concentrations are more influential in mixed-phase partitioning than those in INP concentrations.

  6. Supply- and demand-side effects of power sector planning with demand-side management options and SO2 emission constraints

    International Nuclear Information System (INIS)

    Shrestha, R.M.; Marpaung, C.O.P.

    2005-01-01

    This paper examines the implications of SO 2 emission mitigation constraints in the power sector planning in Indonesia--a developing country--during 2003-2017 from a long term integrated resource planning perspective. A decomposition model is developed to assess the contributions of supply- and demand-side effects to the total changes in CO 2 , SO 2 and NO x emissions from the power sector due to constraints on SO 2 emissions. The results of the study show that both the supply- and demand-side effects would act towards the reduction of CO 2 , SO 2 and NO x emissions. However, the supply-side effect would play the dominant role in emission mitigations from the power sector in Indonesia. The average incremental SO 2 abatement cost would increase from US$ 970 to US$ 1271 per ton of SO 2 , while electricity price would increase by 2-18% if the annual SO 2 emission reduction target is increased from 10% to 25%

  7. Determination of the photolysis rate coefficient of monochlorodimethyl sulfide (MClDMS) in the atmosphere and its implications for the enhancement of SO2 production from the DMS + Cl2 reaction.

    Science.gov (United States)

    Copeland, G; Lee, E P F; Williams, R G; Archibald, A T; Shallcross, D E; Dyke, J M

    2014-01-01

    In this work, the photolysis rate coefficient of CH3SCH2Cl (MClDMS) in the lower atmosphere has been determined and has been used in a marine boundary layer (MBL) box model to determine the enhancement of SO2 production arising from the reaction DMS + Cl2. Absorption cross sections measured in the 28000-34000 cm(-1) region have been used to determine photolysis rate coefficients of MClDMS in the troposphere at 10 solar zenith angles (SZAs). These have been used to determine the lifetimes of MClDMS in the troposphere. At 0° SZA, a photolysis lifetime of 3-4 h has been obtained. The results show that the photolysis lifetime of MClDMS is significantly smaller than the lifetimes with respect to reaction with OH (≈ 4.6 days) and with Cl atoms (≈ 1.2 days). It has also been shown, using experimentally derived dissociation energies with supporting quantum-chemical calculations, that the dominant photodissocation route of MClDMS is dissociation of the C-S bond to give CH3S and CH2Cl. MBL box modeling calculations show that buildup of MClDMS at night from the Cl2 + DMS reaction leads to enhanced SO2 production during the day. The extra SO2 arises from photolysis of MClDMS to give CH3S and CH2Cl, followed by subsequent oxidation of CH3S.

  8. THE DETERMINATION THE POLLUTION EMISSIONS OF SO2, NOX, CO, CO2 AND O2 FROM THE CHANNELS OF BURNT GAS ON BOILER OF 420 T/H - STEAM, IN THE SIGHT APPLICATION PROCEEDING TO REDUCE OF THESE

    Directory of Open Access Journals (Sweden)

    Valentin Nedeff

    2007-03-01

    Full Text Available The work present the results obtained after dynamic analyze the pollution emissions of SO2, NOx, CO, CO2 and O2 on evacuation channels of burnt gas on boiler of 420 t/h steam, having right the basic combustible the lignite, and auxiliary combustible the fuel oil and the natural gas. The values of pollution emission was analyze beside the admissible maxims values required by European legislation for Romania in the year 2005. The conclusion elaborated it adverted to: the values of oxides azoth, carry they frame in the limits provide in Environmental Authorization, under 60 mg/Nmc on 6% oxygen, the concentration values of SO2 which was bigger in report with one authorized comprised between 3500-3900 mg/Nmc confronted by 3400 mg/Nm. For integration in the foresee Government Decision 541/2003 aren't sufficient just proceeding of below reduce SO2, must take and another measures such as: get the fuel with quantity of sulphur 0.5% and with a content of ash below 35%.

  9. First-principles study of SO2 sensors based on phosphorene and its isoelectronic counterparts: GeS, GeSe, SnS, SnSe

    Science.gov (United States)

    Guo, Shiying; Yuan, Lu; Liu, Xuhai; Zhou, Wenhan; Song, Xiufeng; Zhang, Shengli

    2017-10-01

    Phosphorene and its isoelectronic counterparts, such as GeS, GeSe, SnS and SnSe monolayers, show great potential in electrical and sensing applications. Here, we study the SO2 sensing properties of phosphorene and its isoelectronic counterparts by first-principles calculations. Results predict that the SO2 molecule as electron acceptor holds high adsorption strength with the five monolayer substrates, especially for SnS and SnSe monolayers. Moreover, the electronic properties of the five substrates can be modified by the SO2 molecule, together with distinct charge transfer, rendering them promising for application as a high-performance gas sensor.

  10. Degassing patterns of Tungurahua volcano (Ecuador) during the 1999-2006 eruptive period, inferred from remote spectroscopic measurements of SO2 emissions

    OpenAIRE

    Arellano, S. R.; Hall, M.; Samaniego, Pablo; Le Pennec, Jean-Luc; Ruiz, A.; Molina, I.; Yepes, H.

    2008-01-01

    This paper presents the results of 7 years (Aug. 1999-Oct. 2006) of SO2 gas measurements during the ongoing eruption of Tungurahua volcano, Ecuador. From 2004 onwards, the operation of scanning spectrometers has furnished high temporal resolution measurements of SO2 flux, enabling this dataset to be correlated with other datasets, including seismicity. The emission rate of SO2 during this period ranges from less than 100 to 35,000 tonnes/day (t d(-1)) with a mean daily emission rate of 1458 t...

  11. Fuel-based inventory of NOx and SO2 emissions from motor vehicles in the Hiroshima Prefecture, Japan

    International Nuclear Information System (INIS)

    Nurrohim, Agus; Sakugawa, Hiroshi

    2005-01-01

    In order to attain the 2010 target of reducing national greenhouse gases by 6% to the 1990 level, with reference to the Kyoto Protocol, the Government of Japan has planned and implemented some measures, as well as related policies. This paper discusses the possible impact of these measures on the nitrogen-oxide and sulfur-dioxide emissions from road vehicles in the Hiroshima Prefecture (ca. 3 million population). The number of road vehicles based on vehicle and fuel types in the Hiroshima Prefecture for 1990-2000 are presented, as well as projections for the years 2005 and 2010 using the Gompertz model. Three scenarios were developed to assess the emissions, referring to the possible achievement of related measures and policies as well as new vehicle technologies. Prediction results show that nitrogen-oxide emissions may be decreased from 14.7 kton in 1990 to 9.3 kton in 2010 if Japanese energy-policy and new vehicle developments are successfully implemented. If they are less successfully implemented, the emissions will decrease slightly to 14 kton, in which the decrease of emissions was mostly from gasoline vehicle. The emission of sulfur dioxide was projected to decrease from 1.2 kton in 1990 to within the range 0.45-0.49 kton by 2010, as a result of measures to reduce sulfur content in diesel oil

  12. Surface interaction of H2S, SO2, and SO3 on fullerene-like gallium nitride (GaN) nanostructure semiconductor

    Science.gov (United States)

    Salimifard, M.; Rad, A. Shokuhi; Mahanpoor, K.

    2017-10-01

    Density functional theory (DFT) using MPW1PW91 and B3LYP hybrid functionals was utilized for quantum-based investigations of three major sulfur compounds (H2S, SO2, and SO3) adsorption onto fullerene-like Ga12N12 nanocluster. All chemicals showed high chemisorption with the order of SO3>SO2>>H2S. Results of charge analysis showed that during adsorption, transfer of charge is from H2S to nanocluster while reverse direction of charge transfer is found for SO2 and SO3 molecules. Partial dissociation is found for adsorbates especially for SO2 and SO3 molecules. Results of thermochemistry analysis show negative values for enthalpy and Gibbs free energy of adsorption, confirming exothermic spontaneous process. Analysis of frontier molecular orbital (FMO) showed important role of orbital hybridizing towards formation of new bonds upon adsorption. As a result, we introduce Ga12N12 nanocluster as a strong adsorbent for sulfur compounds.

  13. OMI/Aura Sulfur Dioxide (SO2) Total Column Daily L3 Best Pixel Global 0.25deg Lat/Lon Grid V003

    Data.gov (United States)

    National Aeronautics and Space Administration — The OMI/Aura Level-3e SO2 Data Product OMSO2e (Version 003) is now available from the NASA Goddard Earth Sciences Data and Information Services Center (GES DISC) for...

  14. Fermentative high-titer ethanol production from Douglas-fir forest residue without detoxification using SPORL: high SO2 loading at low temperature

    Science.gov (United States)

    Feng Gu; William Gilles; Roland Gleisner; J.Y. Zhu

    2016-01-01

    This study evaluated high sulfur dioxide (SO2) loading in applying Sulfite Pretreatment to Overcome the Recalcitrance of Lignocelluloses (SPORL) to Douglas-fir forest residue (FS-10) for ethanol production through yeast fermentation. Three pretreatments were conducted at 140

  15. Spatial and Temporal Distribution of NO2 and SO2 in Inner Mongolia Urban Agglomeration Obtained from the Combination of Satellite Remote Sensing and Ground Observations

    Science.gov (United States)

    Zheng, C.; Zhao, C.

    2017-12-01

    Nitrogen dioxide (NO2) and sulfur dioxide (SO2) are important influential factors to the urban air quality, atmospheric chemistry and climate change. Based on the combination of tropospheric NO2 and SO2 column density product derived from OMI satellite with the ground station observations, this study analyzed the spatial-temporal distribution characteristic of NO2 and SO2 in Inner Mongolia urban agglomerations. In terms of long-term changing trend, NO2 increased continually from 2005 to 2011 at 14.3% per year and then decreased from 2011 to 2016 (8.1% per year). As for SO2, there is a consistent increase from 2005 to 2007 at 9.7% per year. During the period of 2007 to 2016, despite of a peak value in 2011, it showed a decreasing trend (1.6% per year) as a whole. With regard to the spatial pattern of NO2, the highest levels of pollution occur in Hohhot and Baotou, followed by Wuhai and Ordos, the least polluted area is in Bayannur. Compared with NO2, the SO2 spatial distribution is slightly different. The pollution of SO2 is the most serious in Wuhai, followed by Hohhot and Baotou, and it is the lightest in Ordos and Bayannur. The diurnal variation of NO2 and SO2 is basically the same, which shows a decrease from 0:00 to 6:00, then rises, and reaches a peak at 8:00, and decreases from 8:00 to 15:00, which is highly related to the diurnal variation of anthropogenic emission and boundary layer height. The long-term spatial-temporal distribution of NO2 and SO2 are closely related to human activities, while meteorology also plays an important role for their diurnal and seasonal variations.

  16. Regional oxygen saturation index (rSO2) in brachioradialis and deltoid muscle. Correlation and prognosis in patients with respiratory sepsis.

    Science.gov (United States)

    Rodríguez, A; Claverias, L; Marín, J; Magret, M; Rosich, S; Bodí, M; Trefler, S; Pascual, S; Gea, J

    2015-03-01

    To compare oxygen saturation index (rSO2) obtained simultaneously in two different brachial muscles. Prospective and observational study. Intensive care unit. Critically ill patients with community-acquired pneumonia. Two probes of NIRS device (INVOS 5100) were simultaneously placed on the brachioradialis (BR) and deltoid (D) muscles. rSO2 measurements were recorded at baseline (ICU admission) and at 24h. Demographic and clinical variables were registered. Pearson's correlation coefficient was used to assess the association between continuous variables. The consistency of the correlation was assessed using the intraclass correlation coefficient (ICC) and Bland-Altman plot. The predictive value of the rSO2 for mortality was calculated by ROC curve. Nineteen patients were included with an ICU mortality of 21.1%. The rSO2 values at baseline and at 24h were significantly higher in D than in BR muscle. Values obtained simultaneously in both limbs showed a strong correlation and adequate consistency: BR (r=0.95; p0.001) but a wide limit of agreement. Non-survivors had rSO2 values significantly lower than survivors at all times of the study. No patient with rSO2 >60% in BR died, and only 17.6% died with an rSO2 value >60% in D. Both muscles showed consistent discriminatory power for mortality. Both BR and D muscles were appropriate for measuring rSO2. Copyright © 2013 Elsevier España, S.L.U. and SEMICYUC. All rights reserved.

  17. Complete Genome Sequence of Salmonella enterica Serovar Typhimurium Strain SO2 (Sequence Type 302) Isolated from an Asymptomatic Child in Mexico

    Science.gov (United States)

    Calva, Edmundo; Puente, José L.; Zaidi, Mussaret B.

    2016-01-01

    The complete genome sequence of Salmonella enterica serovar Typhimurium strain SO2, isolated from an asymptomatic child in Mexico, was determined using PacBio single-molecule real-time technology. Strain SO2 has six complete chromosomal prophages, namely, ST104, Gifsy-2, ST64B, Gifsy-1, ELPhiS, and FSL SP-004, and carries a Salmonella virulence plasmid. PMID:27081133

  18. An automated SO2 camera system for continuous, real-time monitoring of gas emissions from Kīlauea Volcano's summit Overlook Crater

    Science.gov (United States)

    Kern, Christoph; Sutton, Jeff; Elias, Tamar; Lee, Lopaka; Kamibayashi, Kevan; Antolik, Loren; Werner, Cynthia

    2015-07-01

    SO2 camera systems allow rapid two-dimensional imaging of sulfur dioxide (SO2) emitted from volcanic vents. Here, we describe the development of an SO2 camera system specifically designed for semi-permanent field installation and continuous use. The integration of innovative but largely ;off-the-shelf; components allowed us to assemble a robust and highly customizable instrument capable of continuous, long-term deployment at Kīlauea Volcano's summit Overlook Crater. Recorded imagery is telemetered to the USGS Hawaiian Volcano Observatory (HVO) where a novel automatic retrieval algorithm derives SO2 column densities and emission rates in real-time. Imagery and corresponding emission rates displayed in the HVO operations center and on the internal observatory website provide HVO staff with useful information for assessing the volcano's current activity. The ever-growing archive of continuous imagery and high-resolution emission rates in combination with continuous data from other monitoring techniques provides insight into shallow volcanic processes occurring at the Overlook Crater. An exemplary dataset from September 2013 is discussed in which a variation in the efficiency of shallow circulation and convection, the processes that transport volatile-rich magma to the surface of the summit lava lake, appears to have caused two distinctly different phases of lake activity and degassing. This first successful deployment of an SO2 camera for continuous, real-time volcano monitoring shows how this versatile technique might soon be adapted and applied to monitor SO2 degassing at other volcanoes around the world.

  19. O3 and SO2 sensing concept on extended surface of B12N12 nanocages modified by Nickel decoration: A comprehensive DFT study

    Science.gov (United States)

    Rad, Ali Shokuhi; Ayub, Khurshid

    2017-07-01

    Adsorption of SO2 and O3 molecules on pristine boron nitride (B12N12) and Ni-decorated B12N12 nano-cages has been systemically investigated through density functional theory (DFT) methods. Adsorption energies (thermodynamics), bond distances, charge analysis, dipole moments, orbital analysis and density of states are calculated by van der Waals DFT method (MPW1PW91) functional. The adsorption energies of O3 and SO2 on pristine B12N12 are about -143.8 and -14.0 kJ mol-1, respectively. The interaction energies of O3 and SO2 with pristine B12N12 are indicative of chemisorption and physisorption, respectively. Ni-decorated B12N12 (Ni@BN) enhances adsorption of both O3 and SO2 species. The interaction energies for adsorption of SO2 are about -166 and -277 kJ mol-1 whereas the corresponding energies for O3 are -362 and -396 kJ mol-1 for configuration A and B, respectively. These observations show that functionalized B12N12 are highly sensitive toward SO2 and O3 molecules.

  20. On Elasticity Measurement in Cloud Computing

    Directory of Open Access Journals (Sweden)

    Wei Ai

    2016-01-01

    Full Text Available Elasticity is the foundation of cloud performance and can be considered as a great advantage and a key benefit of cloud computing. However, there is no clear, concise, and formal definition of elasticity measurement, and thus no effective approach to elasticity quantification has been developed so far. Existing work on elasticity lack of solid and technical way of defining elasticity measurement and definitions of elasticity metrics have not been accurate enough to capture the essence of elasticity measurement. In this paper, we present a new definition of elasticity measurement and propose a quantifying and measuring method using a continuous-time Markov chain (CTMC model, which is easy to use for precise calculation of elasticity value of a cloud computing platform. Our numerical results demonstrate the basic parameters affecting elasticity as measured by the proposed measurement approach. Furthermore, our simulation and experimental results validate that the proposed measurement approach is not only correct but also robust and is effective in computing and comparing the elasticity of cloud platforms. Our research in this paper makes significant contribution to quantitative measurement of elasticity in cloud computing.

  1. Modeling study of cloud droplet nucleation and in-cloud sulfate production during the Sanitation of the Atmosphere (SANA) 2 campaign

    Science.gov (United States)

    Liu, Xiaohong; Seidl, Winfried

    1998-01-01

    Based upon the measurements of vertical profiles of gaseous SO2, H2O2, O3, and meteorological parameters from aircraft and of the aerosol chemical composition and gaseous NH3, HNO3, and SO2 at the surface in southeastern Germany (Melpitz) during the Sanitation of the Atmosphere (SANA) 2 campaign, realistic modeling of cloud droplet nucleation and in-cloud sulfate production was performed with an explicit microphysical cloud model with size-resolved chemistry and cloud top entrainment. For the fair weather cumulus observed during the measurements, the calculated cloud droplet number concentrations could be as high as 2000 cm-3 (and precloud aerosol sulfate up to 9.1 μg m-3), indicating strong sulfur pollution at Melpitz during the campaign. The in-cloud sulfate production is within 1.5-5.0 μg m-3, depending on the initial gaseous NH3 concentration in the parcel. This result shows the necessity of gaseous NH3 vertical profile measurements. Entrainment can reduce the cloud droplet number concentration and cause the distribution of in-cloud produced sulfate to shift toward larger particle sizes. Under the cases we studied, we do not find a significant effect of cloud top gaseous H2O2 entrainment on the in-cloud sulfate production. For the adiabatic cases the departure of bulk water H2O2 from the Henry's law equilibrium is very small. When entrainment included, however, bulk water H2O2 concentrations could be clearly less than the equilibrium values, and the deficiencies are higher (>20%) for droplets larger than 10 μm radius. Our results suggest that entrainment could be one of the important factors to account for the measured H2O2 deficiency in cloud water.

  2. Estimation of Diseases and Mortality Attibuted to Atmospheric NO2 and SO2 Using AirQ Model in Hamadan City, Iran

    Directory of Open Access Journals (Sweden)

    Leili M

    2017-03-01

    Full Text Available Introduction: NO 2 and SO2 as gaseous air pollutants are involved in many global air accidents, and are respiratory tract irritants that can cause numerous health effcts in humans. Threfore, due to the necessity of studies in this fild and the absence of any similar study in the city of Hamadan, the aim of this study was quantifiation of health effcts attibuted to NO 2 and SO2 in Hamadan city of Iran during years 2014 and 2015. Methods: Ths was a cross-sectional study. Primarily, required criteria pollutants and meteorological data were obtained from the environmental protection agency and meteorological agency of Hamadan city, respectively. Th obtained data were validated using the World Health Organization WHO( criteria. Required statistical indices were calculated and according to baseline incidence, relative risk and exposed populations, the diffrent effcts of pollutants were assessed. Results: According to the results, the average annual concentration of NO2 and SO2 was 1.7 and 1.6 times more than the standard, respectively. With central relative risk, the estimated attibuted portion for total mortality attibuted to NO2 and SO2 was 1.74 and 0.92, respectively, which is equal to death of 51.9 and 27.3 individuals during years 2014 and 2015, respectively. Conclusion: As a result, it should be stated that most of the adverse health effcts attibuted to SO 2 and NO2 were observed in concentration ranges from 20 to 49 and 40 to 89 micrograms per cubic meter, respectively. Ths indicated that the concentration distribution of NO2 was wider than SO 2. It can also be concluded that investigated pollutants NO2 and SO2( had signifiant adverse effcts on the residents of Hamadan city and before further increase in the effcts, preventive measures should be taken by relevant authorities

  3. Mortality and morbidity due to exposure to Ambient NO2, SO2, and O3in Isfahan in 2013–2014

    Directory of Open Access Journals (Sweden)

    Ali Abdolahnejad

    2018-01-01

    Full Text Available Background: The presence of air pollutants such as CO, NO2, SO2, O3, and PM in the ambient air mainly emitted from fossil fuels combustion has become a major health concern. The aims of this study were to estimate the attribution of NO2, SO2, and O3 in the premature deaths and prevalence of cardiovascular and respiratory diseases in Isfahan in 2013–2014. Methods: In this study, short-term health effects (total mortality, cardiovascular and respiratory mortality, chronic obstructive pulmonary disease, and acute myocardial infarction of exposure NO2, SO2, and O3 on the population of Isfahan were assessed using AirQ 2.2.3 software suggested by the World Health Organization (WHO. Results: The result showed that from nonaccident total mortality in 2013–2014 in Isfahan, the attributable proportion related to NO2, SO2, and O3 were 1.03% (109 cases, 3.46% (365 cases, and 1.29% (136 cases, respectively. The percentage of days that people were exposed to the highest concentration of NO2 (40–49 μg/m3, SO2 (60–69 μg/m3, and O3 (40–49 μg/m3 was 34.46%, 16.85%, and 42.74% of a year, respectively. Total mortality attributed to NO2, SO2, and O3exposure was 0.36%, 0.79%, and 0.83%, respectively. Conclusions: The concentrations of NO2and SO2were upper than the WHO guidelines. The Air-Q software in spite of its limitations can provide useful information regarding the health outcome of the air pollutants. The results estimated in this study were considerable. This information can help the health authorities and policy makers to draw suitable strategies and fulfill effective emission control programs.

  4. Improved optical flow velocity analysis in SO2 camera images of volcanic plumes - implications for emission-rate retrievals investigated at Mt Etna, Italy and Guallatiri, Chile

    Science.gov (United States)

    Gliß, Jonas; Stebel, Kerstin; Kylling, Arve; Sudbø, Aasmund

    2018-02-01

    Accurate gas velocity measurements in emission plumes are highly desirable for various atmospheric remote sensing applications. The imaging technique of UV SO2 cameras is commonly used to monitor SO2 emissions from volcanoes and anthropogenic sources (e.g. power plants, ships). The camera systems capture the emission plumes at high spatial and temporal resolution. This allows the gas velocities in the plume to be retrieved directly from the images. The latter can be measured at a pixel level using optical flow (OF) algorithms. This is particularly advantageous under turbulent plume conditions. However, OF algorithms intrinsically rely on contrast in the images and often fail to detect motion in low-contrast image areas. We present a new method to identify ill-constrained OF motion vectors and replace them using the local average velocity vector. The latter is derived based on histograms of the retrieved OF motion fields. The new method is applied to two example data sets recorded at Mt Etna (Italy) and Guallatiri (Chile). We show that in many cases, the uncorrected OF yields significantly underestimated SO2 emission rates. We further show that our proposed correction can account for this and that it significantly improves the reliability of optical-flow-based gas velocity retrievals. In the case of Mt Etna, the SO2 emissions of the north-eastern crater are investigated. The corrected SO2 emission rates range between 4.8 and 10.7 kg s-1 (average of 7.1 ± 1.3 kg s-1) and are in good agreement with previously reported values. For the Guallatiri data, the emissions of the central crater and a fumarolic field are investigated. The retrieved SO2 emission rates are between 0.5 and 2.9 kg s-1 (average of 1.3 ± 0.5 kg s-1) and provide the first report of SO2 emissions from this remotely located and inaccessible volcano.

  5. Workshop on Learning Technology for Education in Cloud

    CERN Document Server

    Rodríguez, Emilio; Santana, Juan; Prieta, Fernando

    2012-01-01

    Learning Technology for Education in Cloud investigates how cloud computing can be used to design applications to support real time on demand learning using technologies. The workshop proceedings provide opportunities for delegates to discuss the latest research in TEL (Technology Enhanced Learning) and its impacts for learners and institutions, using cloud.   The Workshop on Learning Technology for Education in Cloud (LTEC '12) is a forum where researchers, educators and practitioners came together to discuss ideas, projects and lessons learned related to the use of learning technology in cloud, on the 11th-13th July at Salamanca in Spain.

  6. Sulfur dioxide (SO2 as observed by MIPAS/Envisat: temporal development and spatial distribution at 15–45 km altitude

    Directory of Open Access Journals (Sweden)

    M. Höpfner

    2013-10-01

    Full Text Available We present a climatology of monthly and 10° zonal mean profiles of sulfur dioxide (SO2 volume mixing ratios (vmr derived from MIPAS/Envisat measurements in the altitude range 15–45 km from July 2002 until April 2012. The vertical resolution varies from 3.5–4 km in the lower stratosphere up to 6–10 km at the upper end of the profiles, with estimated total errors of 5–20 pptv for single profiles of SO2. Comparisons with the few available observations of SO2 up to high altitudes from ATMOS for a volcanically perturbed situation from ACE-FTS and, at the lowest altitudes, with stratospheric in situ observations reveal general consistency of the datasets. The observations are the first empirical confirmation of features of the stratospheric SO2 distribution, which have only been shown by models up to now: (1 the local maximum of SO2 at around 25–30 km altitude, which is explained by the conversion of carbonyl sulfide (COS as the precursor of the Junge layer; and (2 the downwelling of SO2-rich air to altitudes of 25–30 km at high latitudes during winter and its subsequent depletion on availability of sunlight. This has been proposed as the reason for the sudden appearance of enhanced concentrations of condensation nuclei during Arctic and Antarctic spring. Further, the strong increase of SO2 to values of 80–100 unit{pptv} in the upper stratosphere through photolysis of H2SO4 has been confirmed. Lower stratospheric variability of SO2 could mainly be explained by volcanic activity, and no hints of a strong anthropogenic influence have been found. Regression analysis revealed a QBO (quasi-biennial oscillation signal of the SO2 time series in the tropics at about 30–35 km, an SAO (semi-annual oscillation signal at tropical and subtropical latitudes above 32 km and annual periodics predominantly at high latitudes. Further, the analysis indicates a correlation with the solar cycle in the tropics and southern subtropics above 30 km

  7. The effect of wind velocity, air temperature and humidity on NH 3 and SO 2 transfer into bean leaves ( phaseolus vulgaris L.)

    Science.gov (United States)

    van Hove, L. W. A.; Vredenberg, W. J.; Adema, E. H.

    The influence of wind velocity, air temperature and vapour pressure deficit of the air (VPD) on NH 3 and SO 2 transfer into bean leaves ( Phaseolus vulgaris L.) was examined using a leaf chamber. The measurements suggested a transition in the properties of the leaf boundary layer at a wind velocity of 0.3-0.4 ms -1 which corresponds to a Recrit value of about 2000. At higher wind velocities the leaf boundary layer resistance ( rb) was 1.5-2 times lower than can be calculated from the theory. Nevertheless, the assessed relationships between rb and wind velocity appeared to be similar to the theoretical derived relationship for rb. The NH 3 flux and in particular the SO 2 flux into the leaf strongly increased at a VPD decline. The increase of the NH 3 flux could be attributed to an increase of the stomatal conductance ( gs). However, the increase of the SO 2 flux could only partly be explained by an increase of gs. An apparent additional uptake was also observed for the NH 3 uptake at a low temperature and VPD. The SO 2 flux was also influenced by air temperature which could be explained by a temperature effect on gs. The results suggest that calculation of the NH 3 and SO 2 flux using data of gs gives a serious understimation of the real flux of these gases into leaves at a low temperature and VPD.

  8. THE EFFECT OF IRRADIATION DOSE AND AMMONIA CONCENTRATION ON THE APPLICATION OF ELECTRON BEAM FOR TREATMENT GASES POLLUTION OF SO2AND NOX

    Directory of Open Access Journals (Sweden)

    Erizal Erizal

    2010-06-01

    Full Text Available The application of electron beam for treatment gases pollution of SO2 and NOx has been studied.  The simulated SO2 and NOx gases stream produced from diesel fuel burning boiler were flown into electron beam chamber. Irradiation was conducted using 1000 keV electron beam machine at the dose up to 8.8 kGy, while   water vapour and the ammonia gas with variation concentration flew into the system during irradiation. The concentrations of the gases change were observed during processes. After evaluation, it was found that by increasing irradiation dose, the concentration of SO2 and NOx gases removal increases.  The efficiency of gases removal may reach 98 % for SO2 and 88 % for NOX at a dose of 8.8 kGy. By increasing ammonia concentration, the efficiency gas removal increases. Besides, by-products from the irradiation yield were sulfate and nitrate salt compound which are possible to be used as a fertilizer.      Keywords: radiation, electron beam, gas pollution, SO2, NOx, ammonia

  9. OMI-measured SO2 in a large-scale national energy industrial base and its effect on the capital city of Xinjiang, Northwest China

    Science.gov (United States)

    Wang, Jinxiang; Mo, Jingyue; Li, Jixiang; Ling, Zaili; Huang, Tao; Zhao, Yuan; Zhang, Xiaodong; Mao, Xiaoxuan; Gao, Hong; Shen, Yanjie; Ma, Jianmin

    2017-10-01

    Although considerable efforts have been made to improve air quality in Urumqi city, the capital of Xinjiang-Uyghur Autonomous Region in northwestern China and one of the ten cities with worst air quality in China, this city is still experiencing heavy air pollution during the wintertime. The satellite remote sensing of air quality using Ozone Monitoring Instrument (OMI) measured data discerned an increasing trend of the planetary boundary layer (PBL) columns of sulfur dioxide (SO2) in Midong national petrochemical and coal chemical industry base from 2005 to 2016, located in the northeast of Urumqi. The increasing trend of OMI columnar SO2 in this area is in contrast to the widespread decreases in SO2 emissions in eastern and southern China. This is mainly induced by rapid development in the energy industry in this region over the past decade under the national strategy for energy industry expansion and relocation to northwestern China. We observed a significant correlation of OMI columnar SO2 between this energy industrial base and Urumqi city in winter (R = 0.504, p modeling confirms that the occurrence of heavy smog in this capital city during the wintertime was attributed primarily to strong emissions of air contaminants from the energy industrial base under favorable winds. A numerical case study with and without taking the Midong Industry Base into consideration revealed that this industry base contributed 38% to the SO2 level in Urumqi city, offsetting the considerable efforts made by the local government to improve air quality in this city.

  10. The Effect of Deposit Temperature on the Catalytic SO2-to-SO3 Conversion in a Copper Flash Smelting Heat Recovery Boiler

    Science.gov (United States)

    Lehmusto, Juho; Vainio, Emil; Laurén, Tor; Lindgren, Mari

    2018-02-01

    The aim of the work was to study the catalytic role of copper flash smelter deposit in the SO2-to-SO3 conversion. In addition, the effect of process gas temperature at 548 K to 1173 K (275 °C to 900 °C) on the amount of SO3 formed was addressed both in the absence and presence of genuine copper flash smelter deposit. The SO3 conversion rate changed as a function of process gas temperature, peaking at 1023 K (750 °C). A dramatic increase in the SO2-to-SO3 conversion was observed when process dust was present, clearly indicating that process dust catalyzes the SO2-to-SO3 conversion. Based on these results, the catalytic ability of the deposit may lead to sulfuric acid dew point corrosion.

  11. Dynamics and Evolution of SO 2 Gas Condensation around Prometheus-like Volcanic Plumes on Io as Seen by the Near Infrared Mapping Spectrometer

    Science.gov (United States)

    Douté, Sylvain; Lopes, Rosaly; Kamp, Lucas W.; Carlson, Robert; Schmitt, Bernard; Galileo NIMS Team

    2002-08-01

    We analyze a series of spectral image cubes acquired by the Galileo Near Infrared Mapping Spectrometer (NIMS) over the Prometheus region of Io. We use SO 2 frost, a volatile compound ubiquitous on the surface, as a tracer to understand various thermodynamic and volcanic processes acting in this equatorial region. Here we develop a new method to derive, from the 12-wavelength NIMS products, the distribution and physical properties of solid SO 2. This method is based on the inversion of a bidirectional reflectance model on two observed spectral ratios sensitive to (1) the areal abundance of SO 2 and (2) its mean grain size. As a result, reliable and consistent maps of SO 2 abundance and granularity are obtained which can be correlated to distinguish four different physical units. The distribution of these SO 2 units indicates zones of condensation, metamorphism, and sublimation linked with the thermodynamic and volcanic processes of interest. Our maps depict equatorial plains undisturbed by any kind of vigorous volcanic activity over 35-40% of their surface. Elsewhere, 10-20% of the equatorial plains display abnormally low frost coverage which may imply the recent presence of positive thermal anomalies with temperatures in the range 110-200 K. Hot-spots such as Prometheus, Culann, Surya, and Tupan (to mention the most persistent) emit a great variety of gases, some of which will condense at Io's surface near their source regions. Associated fields of freshly condensed SO 2 are easily observed, and deposits of more refractory compounds with higher (e.g., S 8) or lower (e.g., NaCl) molecular weight must also be present (although their exact nature is unknown). Three different mechanisms of emission are proposed for the volatile compounds and supported by the distribution maps. These are (a) the interaction between flowing lava and preexisting volatile deposits on the surface, (b) direct degassing from the lava, an d (c) the eruption of a liquid aquifer from underground

  12. Atmospheric processes affecting the separation of volcanic ash and SO2 in volcanic eruptions: inferences from the May 2011 Grímsvötn eruption

    Directory of Open Access Journals (Sweden)

    F. Prata

    2017-09-01

    Full Text Available The separation of volcanic ash and sulfur dioxide (SO2 gas is sometimes observed during volcanic eruptions. The exact conditions under which separation occurs are not fully understood but the phenomenon is of importance because of the effects volcanic emissions have on aviation, on the environment, and on the earth's radiation balance. The eruption of Grímsvötn, a subglacial volcano under the Vatnajökull glacier in Iceland during 21–28 May 2011 produced one of the most spectacular examples of ash and SO2 separation, which led to errors in the forecasting of ash in the atmosphere over northern Europe. Satellite data from several sources coupled with meteorological wind data and photographic evidence suggest that the eruption column was unable to sustain itself, resulting in a large deposition of ash, which left a low-level ash-rich atmospheric plume moving southwards and then eastwards towards the southern Scandinavian coast and a high-level predominantly SO2 plume travelling northwards and then spreading eastwards and westwards. Here we provide observational and modelling perspectives on the separation of ash and SO2 and present quantitative estimates of the masses of ash and SO2 that erupted, the directions of transport, and the likely impacts. We hypothesise that a partial column collapse or sloughing fed with ash from pyroclastic density currents (PDCs occurred during the early stage of the eruption, leading to an ash-laden gravity intrusion that was swept southwards, separated from the main column. Our model suggests that water-mediated aggregation caused enhanced ash removal because of the plentiful supply of source water from melted glacial ice and from entrained atmospheric water. The analysis also suggests that ash and SO2 should be treated with separate source terms, leading to improvements in forecasting the movement of both types of emissions.

  13. An automated SO2 camera system for continuous, real-time monitoring of gas emissions from Kīlauea Volcano's summit Overlook Crater

    Science.gov (United States)

    Kern, Christoph; Sutton, Jeff; Elias, Tamar; Lee, Robert Lopaka; Kamibayashi, Kevan P.; Antolik, Loren; Werner, Cynthia A.

    2015-01-01

    SO2 camera systems allow rapid two-dimensional imaging of sulfur dioxide (SO2) emitted from volcanic vents. Here, we describe the development of an SO2 camera system specifically designed for semi-permanent field installation and continuous use. The integration of innovative but largely “off-the-shelf” components allowed us to assemble a robust and highly customizable instrument capable of continuous, long-term deployment at Kīlauea Volcano's summit Overlook Crater. Recorded imagery is telemetered to the USGS Hawaiian Volcano Observatory (HVO) where a novel automatic retrieval algorithm derives SO2 column densities and emission rates in real-time. Imagery and corresponding emission rates displayed in the HVO operations center and on the internal observatory website provide HVO staff with useful information for assessing the volcano's current activity. The ever-growing archive of continuous imagery and high-resolution emission rates in combination with continuous data from other monitoring techniques provides insight into shallow volcanic processes occurring at the Overlook Crater. An exemplary dataset from September 2013 is discussed in which a variation in the efficiency of shallow circulation and convection, the processes that transport volatile-rich magma to the surface of the summit lava lake, appears to have caused two distinctly different phases of lake activity and degassing. This first successful deployment of an SO2 camera for continuous, real-time volcano monitoring shows how this versatile technique might soon be adapted and applied to monitor SO2 degassing at other volcanoes around the world.

  14. Atmospheric processes affecting the separation of volcanic ash and SO2 in volcanic eruptions: inferences from the May 2011 Grímsvötn eruption

    Science.gov (United States)

    Prata, Fred; Woodhouse, Mark; Huppert, Herbert E.; Prata, Andrew; Thordarson, Thor; Carn, Simon

    2017-09-01

    The separation of volcanic ash and sulfur dioxide (SO2) gas is sometimes observed during volcanic eruptions. The exact conditions under which separation occurs are not fully understood but the phenomenon is of importance because of the effects volcanic emissions have on aviation, on the environment, and on the earth's radiation balance. The eruption of Grímsvötn, a subglacial volcano under the Vatnajökull glacier in Iceland during 21-28 May 2011 produced one of the most spectacular examples of ash and SO2 separation, which led to errors in the forecasting of ash in the atmosphere over northern Europe. Satellite data from several sources coupled with meteorological wind data and photographic evidence suggest that the eruption column was unable to sustain itself, resulting in a large deposition of ash, which left a low-level ash-rich atmospheric plume moving southwards and then eastwards towards the southern Scandinavian coast and a high-level predominantly SO2 plume travelling northwards and then spreading eastwards and westwards. Here we provide observational and modelling perspectives on the separation of ash and SO2 and present quantitative estimates of the masses of ash and SO2 that erupted, the directions of transport, and the likely impacts. We hypothesise that a partial column collapse or sloughing fed with ash from pyroclastic density currents (PDCs) occurred during the early stage of the eruption, leading to an ash-laden gravity intrusion that was swept southwards, separated from the main column. Our model suggests that water-mediated aggregation caused enhanced ash removal because of the plentiful supply of source water from melted glacial ice and from entrained atmospheric water. The analysis also suggests that ash and SO2 should be treated with separate source terms, leading to improvements in forecasting the movement of both types of emissions.

  15. Evaluation of gases, condensates, and SO2 emissions from Augustine volcano, Alaska: the degassing of a Cl-rich volcanic system

    Science.gov (United States)

    Symonds, R.B.; Rose, William I.; Gerlach, T.M.; Briggs, P.H.; Harmon, R.S.

    1990-01-01

    After the March-April 1986 explosive eruption a comprehensive gas study at Augustine was undertaken in the summers of 1986 and 1987. Airborne COSPEC measurements indicate that passive SO2 emission rates declined exponentially during this period from 380??45 metric tons/day (T/D) on 7/24/86 to 27??6 T/D on 8/24/87. These data are consistent with the hypothesis that the Augustine magma reservoir has become more degassed as volcanic activity decreased after the spring 1986 eruption. Gas samples collected in 1987 from an 870??C fumarole on the andesitic lava dome show various degrees of disequilibrium due to oxidation of reduced gas species and condensation (and loss) of H2O in the intake tube of the sampling apparatus. Thermochemical restoration of the data permits removal of these effects to infer an equilibrium composition of the gases. Although not conclusive, this restoration is consistent with the idea that the gases were in equilibrium at 870??C with an oxygen fugacity near the Ni-NiO buffer. These restored gas compositions show that, relative to other convergent plate volcanoes, the Augustine gases are very HCl rich (5.3-6.0 mol% HCl), S rich (7.1 mol% total S), and H2O poor (83.9-84.8 mol% H2O). Values of ??D and ??18O suggest that the H2O in the dome gases is a mixture of primary magmatic water (PMW) and local seawater. Part of the Cl in the Augustine volcanic gases probably comes from this shallow seawater source. Additional Cl may come from subducted oceanic crust because data by Johnston (1978) show that Cl-rich glass inclusions in olivine crystals contain hornblende, which is evidence for a deep source (>25km) for part of the Cl. Gas samples collected in 1986 from 390??-642??C fumaroles on a ramp surrounding the inner summit crater have been oxidized so severely that restoration to an equilibrium composition is not possible. H and O isotope data suggest that these gases are variable mixtures of seawater, FMW, and meteoric steam. These samples are much

  16. The primary volcanic aerosol emission from Mt Etna: Size-resolved particles with SO2 and role in plume reactive halogen chemistry

    Science.gov (United States)

    Roberts, T. J.; Vignelles, D.; Liuzzo, M.; Giudice, G.; Aiuppa, A.; Coltelli, M.; Salerno, G.; Chartier, M.; Couté, B.; Berthet, G.; Lurton, T.; Dulac, F.; Renard, J.-B.

    2018-02-01

    Volcanoes are an important source of aerosols to the troposphere. Within minutes after emission, volcanic plume aerosol catalyses conversion of co-emitted HBr, HCl into highly reactive halogens (e.g. BrO, OClO) through chemical cycles that cause substantial ozone depletion in the dispersing downwind plume. This study quantifies the sub-to-supramicron primary volcanic aerosol emission (0.2-5 μm diameter) and its role in this process. An in-situ ground-based study at Mt Etna (Italy) during passive degassing co-deployed an optical particle counter and Multi-Gas SO2 sensors at high time resolution (0.1 Hz) enabling to characterise the aerosol number, size-distribution and emission flux. A tri-modal volcanic aerosol size distribution was found, to which lognormal distributions are fitted. Total particle volume correlates to SO2 (as a plume tracer). The measured particle volume:SO2 ratio equates to a sulfate:SO2 ratio of 1-2% at the observed meteorological conditions (40% Relative Humidity). A particle mass flux of 0.7 kg s-1 is calculated for the measured Mt Etna SO2 flux of 1950 tonnes/day. A numerical plume atmospheric chemistry model is used to simulate the role of the hygroscopic primary aerosol surface area and its humidity dependence on volcanic plume BrO and OClO chemistry. As well as predicting volcanic BrO formation and O3 depletion, the model achieves OClO/SO2 in broad quantitative agreement with recently reported Mt Etna observations, with a predicted maximum a few minutes downwind. In addition to humidity - that enhances aerosols surface area for halogen cycling - background ozone is predicted to be an important control on OClO/SO2. Dependence of BrO/SO2 on ambient humidity is rather low near-to-source but increases further downwind. The model plume chemistry also exhibits strong across-plume spatial variations between plume edge and centre.

  17. Determination of empirical models of NOx and SO2 removal efficiency for two steps of combustion gas irradiation system basing on results obtained at EPS Kaweczyn pilot plant

    International Nuclear Information System (INIS)

    Chmielewski, A.G.; Tyminski, B.; Dobrowolski, A.; Licki, J.

    1998-01-01

    A multidimensional regression method has been applied to construct empirical models equations of NO x and SO 2 removal efficiency in e-b process for two stage irradiation system basing on results achieved for EPS Kaweczyn pilot plant. Model equations describe with satisfactory accuracy experimental results, therefore obtained model equations can be used for prediction of NO x and SO 2 removal efficiency in e-b process during two stages irradiation of flue gases particularly in case of scale-up. (author)

  18. The effect of broadband soft X-rays in SO2-containing ices: Implication on the photochemistry of ices towards young stellar objects

    OpenAIRE

    Pilling, S.; Bergantini, A.

    2015-01-01

    We investigate the effects produced mainly by broadband soft X-rays up to 2 keV (plus fast (keV) photoelectrons and low-energy (eV) induced secondary electrons) in the ice mixtures containing H2O:CO2:NH3:SO2 (10:1:1:1) at two different temperatures (50 K and 90 K). The experiments are an attempt to simulate the photochemical processes induced by energetic photons in SO2-containing ices present in cold environments in the ices surrounding young stellar objects (YSO) and in molecular clouds in ...

  19. Low-Temperature Thermal Reactions Between SO2 and H2O2 and Their Relevance to the Jovian Icy Satellites

    Science.gov (United States)

    Loeffler, Mark J.; Hudson, Reggie L.

    2013-01-01

    Here we present first results on a non-radiolytic, thermally-driven reaction sequence in solid H2O +SO2 + H2O2 mixtures at 50-130 K, which produces sulfate (SO(-2)/(4)), and has an activation energy of 53 kJ/mole. We suspect that these results may explain some of the observations related to the presence and distribution of H2O2 across Europa's surface as well as the lack of H2O2 on Ganymede and Callisto.

  20. Spatial and temporal evaluation of long term trend (2005-2014) of OMI retrieved NO2 and SO2 concentrations in Henan Province, China

    Science.gov (United States)

    Zhang, Leishi; Lee, Chih Sheng; Zhang, Ruiqin; Chen, Liangfu

    2017-04-01

    Tropospheric NO2 and SO2 concentrations are of great importance with regard to air quality, atmospheric chemistry, and climate change. Due to lack of surface monitoring stations, this study analyzes long term trend of NO2 and SO2 levels (2005-2014), retrieved from Ozone Monitoring Instrument (OMI) board on the NASA's Aura satellite, in an important region of China - Henan Province. Henan Province, located in North China Plain, has encountered serious air pollution problems including extremely high PM2.5 concentrations and as one of the most polluted region in China. The satellite spatial images clearly show that high levels of both NO2 and SO2 are concentrated in north and northeastern regions with much lower levels observed in other parts of Henan. Both pollutants exhibit the highest levels in winter with the least in summer/spring. The temporal trend analysis based on moving average of deseasonalized and decyclic data indicates that for NO2, there is a continuous increasing pattern from 2005 to 2011 at 6.4% per year, thereafter, it shows a decreasing trend (10.6% per year). As for SO2, the increasing trend is about 16% per year from 2005 to 2007 with decreasing rate 7% per year from 2007 to 2014. The economic development with incredible annual 11% GDP growth in Henan is responsible for increasing levels of NO2 and SO2. The observed decreasing SO2 level starting in 2007 is due to reduced SO2 emission, utilization of flue gas desulfurization (FGD) devices and to some extent, in preparation of Beijing 2008 Olympic Games. On the other hand, increasing vehicle numbers (155% from 2006 to 2012) and coal consumption (37% during the same span), along with the lack of denitration process for removing flue/exhaust gas NOx are responsible for increasing NO2 trend until 2011. The ratio of SO2/NO2 started decreasing in 2007 and dropped significantly from 2011 to 2013 indicating good performance of FGD and ever increasing NOx contribution from mobile sources. Unlike those

  1. What Determines the Ice Polymorph in Clouds?

    Science.gov (United States)

    Hudait, Arpa; Molinero, Valeria

    2016-07-20

    vapor in the tropical tropopause layer, and in polar stratospheric and noctilucent clouds. Our findings support and explain the evolution of the morphology of ice crystals from hexagonal to trigonal symmetry with decreasing temperature, as reported by experiments and in situ measurements in clouds. We conclude that selective growth of the elusive cubic ice polymorph by manipulation of the interfacial properties can likely be achieved at the ice-liquid interface but not at the ice-vapor interface.

  2. Molten V2O5/Cs0.9K0.9Na0.2S2O7 and V2O5/K2S2O7 catalysts as electrolytes in an electrocatalytic membrane separation device for SO2 removal

    DEFF Research Database (Denmark)

    Rasmussen, Søren Birk; Eriksen, Kim Michael; Fehrmann, Rasmus

    2002-01-01

    Bench scale fuel cell tests have been carried out on the SO2 oxidation catalyst systems V2O5/M2S2O7 (M = alkali) used as electrolytes in a standard molten carbonate fuel cell (MCFC) fuel cell setup for removal of SO2 from power plant flue gases. Porous LixNi(1-x)O electrodes were used both as anode...... at approximately 5 mA cm(-2). However, the data obtained during the experiments explain the current limitations of the process, especially in terms of electrolyte wetting capability and acid/base chemistry of the electrolyte....

  3. 40 CFR 60.104 - Standards for sulfur oxides.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standards for sulfur oxides. 60.104... Refineries § 60.104 Standards for sulfur oxides. Each owner or operator that is subject to the requirements... device to reduce SO2 emission, maintain sulfur oxides emissions calculated as SO2 to the atmosphere less...

  4. Study on the adsorption properties of O3, SO2, and SO3 on B-doped graphene using DFT calculations

    International Nuclear Information System (INIS)

    Rad, Ali Shokuhi; Shabestari, Sahand Sadeghi; Mohseni, Soheil; Aghouzi, Samaneh Alijantabar

    2016-01-01

    We investigated the structure, adsorption, electronic states, and charge transfer of O 3 , SO 2 and SO 3 molecules on the surface of a B-doped graphene using density functional theory (DFT). We found weak physisorption of SO 2 (−10.9 kJ/mole, using B3LYP-D) and SO 3 (−15.7 kJ/mole, using B3LYP-D) on the surface of B-doped graphene while there is strong chemisorption for O 3 (−96.3 kJ/mole, using B3LYP-D ) on this surface. Our results suggest the potential of B-doped graphene as a selective sensor/adsorbent for O 3 molecule. We noticed some change in hybridizing of boron from sp 2 to sp 3 upon adsorption of O 3 which cases transformation of the adsorbent from 2D to 3D. - Graphical abstract: The electronic property of B-doped graphene is responsible to highly adsorption of O 3 molecules while the adsorption of SO 2 and SO 3 molecules on this surface exhibits only a weak interaction. - Highlights: • B-doped graphene clearly is n-type semiconductor. • High negatively charge of C-atoms neighboring the boron dopant. • Chemisorption of O 3 and physisorption of SO 2 and SO 3 on the surface of B-doped graphene.

  5. Atmospheric H2S and SO2 as sulfur sources for Brassica juncea and Brassica rapa: Regulation of sulfur uptake and assimilation

    NARCIS (Netherlands)

    Aghajanzadeh, T.; Hawkesford, M.J.; De Kok, L.J.

    2016-01-01

    Brassica juncea and Brassica rapa were able to utilize foliarly absorbed H2S and SO2 as sulfur source for growth and resulted in a decreased sink capacity of the shoot for sulfur supplied by the root and subsequently in a partial decrease in sulfate uptake capacity of the roots. Sulfate-deprived

  6. Atmospheric H2S and SO2 as sulfur source for Brassica juncea and Brassica rapa: Impact on the glucosinolate composition

    NARCIS (Netherlands)

    Aghajanzadeh, T.; Kopriva, S; Hawkesford, M.J.; Koprivova, A.; De Kok, L.J.

    2015-01-01

    The impact of sulfate deprivation and atmospheric H2S and SO2 nutrition on the content and composition of glucosinolates was studied in Brassica juncea and Brasscia rapa. Both species contained a number of aliphatic and indolic glucosinolates. The total glucosinolate content was more than 5.5-fold

  7. OMI/Aura Sulphur Dioxide (SO2) Total Column Daily L2 Global 0.125 deg Lat/Lon Grid V003

    Data.gov (United States)

    National Aeronautics and Space Administration — The OMI/Aura Level-2G SO2 Data Product OMSO2G (Version 003) is now available http://disc.gsfc.nasa.gov/Aura/OMI/omso2g_v003.shtml ) from the NASA Goddard Earth...

  8. The utility of biochemical, physiological and morphological biomarkers of leaf sulfate levels in establishing Brachylaena discolor leaves as a bioindicator of SO2pollution.

    Science.gov (United States)

    Areington, Candyce Ann; Varghese, Boby; Sershen

    2017-09-01

    The negative impacts of air pollution have made monitoring of air quality increasingly important, especially in heavily industrialized areas such as the South Durban Basin (SDB), in South Africa. Bioindicators such as trees can complement conventional air quality monitoring and be used to prioritise vulnerable areas. This study assessed the utility of Brachylaena discolor DC. tree leaves as a bioindicator of sulfur dioxide pollution. This involved correlating ground level sulfur dioxide concentrations ([SO 2 ]) with B. discolor leaf sulfate concentrations ([sulfate]) at three industrial (treatment) sites within the SBD and control site at which [SO 2 ] was significantly lower for all four seasons. Based on this significant positive correlation between the aforementioned (p = 0.005; ρ = 0.667) leaf sulfate levels were related to various biochemical (intracellular hydrogen peroxide production, total aqueous [TAA] and enzymic antioxidants [superoxide dismutase and catalase], lipid peroxidation [LPO] and electrolyte leakage), physiological (leaf chlorophyll fluorescence [LCF] and relative chlorophyll content) and morphological (leaf area [LA]) biomarkers of stress measured on leaves from trees at the treatment and control sites. Annual [SO 2 ] and leaf [sulfate] at the treatments were significantly (p bioindicator of SO 2 pollution. Copyright © 2017 Elsevier Masson SAS. All rights reserved.