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Sample records for air oxidation cwao

  1. Active carbon-ceramic sphere as support of ruthenium catalysts for catalytic wet air oxidation (CWAO) of resin effluent.

    PubMed

    Liu, Wei-Min; Hu, Yi-Qiang; Tu, Shan-Tung

    2010-07-15

    Active carbon-ceramic sphere as support of ruthenium catalysts were evaluated through the catalytic wet air oxidation (CWAO) of resin effluent in a packed-bed reactor. Active carbon-ceramic sphere and ruthenium catalysts were characterized by N(2) adsorption and chemisorption measurements. BET surface area and total pore volume of active carbon (AC) in the active carbon-ceramic sphere increase with increasing KOH-to-carbon ratio, and AC in the sample KC-120 possesses values as high as 1100 m(2) g(-1) and 0.69 cm(3) g(-1) (carbon percentage: 4.73 wt.%), especially. Active carbon-ceramic sphere supported ruthenium catalysts were prepared using the RuCl(3) solution impregnation onto these supports, the ruthenium loading was fixed at 1-5 wt.% of AC in the support. The catalytic activity varies according to the following order: Ru/KC-120>Ru/KC-80>Ru/KC-60>KC-120>without catalysts. It is found that the 3 wt.% Ru/KC-120 catalyst displays highest stability in the CWAO of resin effluent during 30 days. Chemical oxygen demand (COD) and phenol removal were about 92% and 96%, respectively at the reaction temperature of 200 degrees C, oxygen pressure of 1.5 MPa, the water flow rate of 0.75 L h(-1) and the oxygen flow rate of 13.5 L h(-1). PMID:20362394

  2. [Effect of temperature on decomposition of leachates by WAO/CWAO].

    PubMed

    Li, Hai-sheng; Liu, Liang; Li, Yu; Liu, Guang-hui; Wang, Jian; Liu, Hong-liang

    2004-07-01

    Catalytic wet air oxidation (CWAO) is a very effective physical chemistry method to treat organic wastewater. In this experiment, CWAO is employed to reduce the organic compounds in the landfill leachates. Temperature is an important factor in treating leachates by CWAO, so the effect of temperature on the reduction efficiency and decomposition rate of organic pollutants is investigated emphatically and the quantificational relationship is established between the decomposition rates and temperatures used in this study. The function of Co/Bi catalyst for the reduction of landfill leachates is also discussed. The influence of temperature on the degradation of landfill leachates by CWAO is carried out in a sealed environment using catalyst. The resulted information shows that the reduction rate of total organic carbon (TOC) and chemical oxygen demand (COD) increases notably with increase in temperature with or without the catalyst, and that the Elovich equation can describe dynamics course of landfill leachates degradation well. Rate constant k also increases with increase in temperature and the quantificational relationship is established between the rate constant k and temperature; the main reason of pH value reducing rapidly at first and later rising slowly is that a large amount of organic acid is produced in the early period in the reaction and the organic acid is degraded gradually later. Degradation of landfill leachates by CWAO can reach better treatment efficiency in gentle condition with catalyst Co/Bi in this study. The temperature's relatively great impact on the reaction using CWAO is discussed only in the paper and the effects of the other reaction conditions such as oxidant and catalyst dosage and the concentration of wastewater on degrading efficiency by CWAO are to be focused on. PMID:15515953

  3. Catalytic and non-catalytic wet air oxidation of sodium dodecylbenzene sulfonate: kinetics and biodegradability enhancement.

    PubMed

    Suárez-Ojeda, María Eugenia; Kim, Jungkwon; Carrera, Julián; Metcalfe, Ian S; Font, Josep

    2007-06-18

    Wet air oxidation (WAO) and catalytic wet air oxidation (CWAO) were investigated as suitable precursors for the biological treatment of industrial wastewater containing sodium dodecylbenzene sulfonate (DBS). Two hours WAO semi-batch experiments were conducted at 15 bar of oxygen partial pressure (P(O2)) and at 180, 200 and 220 degrees C. It was found that the highest temperature provides appreciable total organic carbon (TOC) and chemical oxygen demand (COD) abatement of about 42 and 47%, correspondingly. Based on the main identified intermediates (acetic acid and sulfobenzoic acid) a reaction pathway for DBS and a kinetic model in WAO were proposed. In the case of CWAO experiments, seventy-two hours tests were done in a fixed bed reactor in continuous trickle flow regime, using a commercial activated carbon (AC) as catalyst. The temperature and P(O2) were 140-160 degrees C and 2-9 bar, respectively. The influence of the operating conditions on the DBS oxidation, the occurrence of oxidative coupling reactions over the AC, and the catalytic activity (in terms of substrate removal) were established. The results show that the AC without any supported active metal behaves bi-functional as adsorbent and catalyst, giving TOC conversions up to 52% at 160 degrees C and 2 bar of P(O2), which were comparable to those obtained in WAO experiments. Respirometric tests were completed before and after CWAO and to the main intermediates identified through the WAO and CWAO oxidation route. Then, the readily biodegradable COD (COD(RB)) of the CWAO and WAO effluents were found. Taking into account these results it was possible to compare whether or not the CWAO or WAO effluents were suitable for a conventional activated sludge plant inoculated with non adapted culture. PMID:17363148

  4. Treatment of refractory nano-filtration reject from a tannery using Pd-catalyzed wet air oxidation.

    PubMed

    Tripathi, Pranav K; Rao, Nageswara N; Chauhan, Chetan; Pophali, Girish R; Kashyap, Sanjay M; Lokhande, Satish K; Gan, Lihua

    2013-10-15

    We attempted catalytic wet air oxidation (CWAO) of nanofiltration (NF)-reject using Pd based catalyst viz., Pd/activated charcoal (AC) and PdCl2 with the objective of degradation of refractory organic pollutants. Refractory organic pollutants in NF-reject before and after WAO and CWAO were confirmed by GC-MS analysis. Experiments were conducted to investigate the effects of temperature, catalyst dosage and air partial pressure on the rate of removal of total organic carbon (TOC). The reaction kinetics can be conveniently described by considering two-stage first order kinetics. The use of Pd/AC afforded 85% TOC removal, the corresponding rate constant (k) was 2.90 ± 0.075 × 10(-3)min(-1) (Pd/AC, 100mg/L; T, 473.15K; Pair, 0.69 MPa). On the other hand, 75% TOC was removed with k=2.31 ± 0.075 × 10(-3)min(-1) using Pd(2+) catalyst (Pd(2+), 16.66 mg/L; T, 473.15K; Pair, 0.69 MPa). The observed rate of mineralization under Pd-catalyzed conditions was significantly higher than that of the uncatalyzed oxidation (41%) under the similar experimental conditions. Catalyst stability experiments were performed and TEM, SEM, XRD, Raman and XPS characterization data collected. Despite some morphological transformation of support, Pd catalyst was stable under CWAO conditions. PMID:23911829

  5. Treatment of aniline by catalytic wet air oxidation: comparative study over CuO/CeO2 and NiO/Al2O3.

    PubMed

    Ersöz, Gülin; Atalay, Süheyda

    2012-12-30

    The treatment of aniline by catalytic wet air oxidation (CWAO) was studied in a bubble reactor. The experiments were performed to investigate the effects of catalyst loading, temperature, reaction time, air flow rate, and pressure on aniline removal. The catalytic effects of the prepared nanostructured catalysts, CuO/CeO(2) (10% wt) and NiO/Al(2)O(3) (10% wt), on the CWAO treatment efficiency were also examined and compared. The prepared catalysts seem to be active having an aniline removal of 45.7% with CuO/CeO(2) and 41.9% with NiO/Al(2)O(3). The amount of N(2) formed was approximately the same for both of the catalysts. PMID:23041516

  6. Novel Na2Mo4O13/α-MoO3 hybrid material as highly efficient CWAO catalyst for dye degradation at ambient conditions

    NASA Astrophysics Data System (ADS)

    Zhang, Zhang; Yang, Ruoyan; Gao, Yanshan; Zhao, Yufei; Wang, Junyang; Huang, Liang; Guo, Jiang; Zhou, Tuantuan; Lu, Peng; Guo, Zhanhu; Wang, Qiang

    2014-10-01

    We report a novel hybrid material Na2Mo4O13/α-MoO3 as highly efficient catalytic wet air oxidation (CWAO) catalyst, which showed the highest ever activity at room temperature and atmosphere pressure for the degradation of cationic red GTL. SEM and TEM analyses indicated that this hybrid catalyst has bamboo-shaped nanofiber morphology. In view of practical applications, the influence of some key parameters including operation temperature, catalyst calcination temperature, and the volume of dye wastewater have been optimized. The mechanism for the superior catalytic performance was investigated. XRD, XPS, and ESR suggested the Na2Mo4O13/α-MoO3 hybrid catalyst possesses more O2- ions in the oxygen deficient regions than neat α-MoO3, promoting the formation of active .OH radicals and resulting in a higher activity. Considering the facile preparation and its superior activity, this novel catalyst is promising for practical dye wastewater treatment.

  7. Supported noble metal catalysts in the catalytic wet air oxidation of industrial wastewaters and sewage sludges.

    PubMed

    Besson, M; Descorme, C; Bernardi, M; Gallezot, P; di Gregorio, F; Grosjean, N; Minh, D Pham; Pintar, A

    2010-12-01

    This paper reviews some catalytic wet air oxidation (CWAO) investigations of industrial wastewaters over platinum and ruthenium catalysts supported on TiO2 and ZrO2 formulated to be active and resistant to leaching, with particular focus on the stability of the catalyst. Catalyst recycling experiments were performed in batch reactors and long-term stability tests were conducted in trickle-bed reactors. The catalyst did not leach upon treatment of Kraft bleaching plant and olive oil mill effluents, and could be either recycled or used for long periods of time in continuous reactors. Conversely, these catalysts were rapidly leached when used to treat effluents from the production of polymeric membranes containing N,N-dimethylformamide. The intermediate formation of amines, such as dimethylamine and methylamine with a high complexing capacity for the metal, was shown to be responsible for the metal leaching. These heterogeneous catalysts also deactivated upon CWAO of sewage sludges due to the adsorption of the solid organic matter. Pre-sonication of the sludge to disintegrate the flocs and improve solubility was inefficient. PMID:21214003

  8. Degradation process analysis of the azo dyes by catalytic wet air oxidation with catalyst CuO/γ-Al2O3.

    PubMed

    Hua, Li; Ma, Hongrui; Zhang, Lei

    2013-01-01

    Three azo dyes (Methyl Orange, Direct Brown and Direct Green) were treated by catalytic wet air oxidation (CWAO) with the catalysts CuO/γ-Al(2)O(3) prepared by consecutive impregnation. The relationship of decolorization extent, chemical oxygen demand (COD) removal extent and total organic carbon (TOC) in dye solution were investigated. The results indicated that the CuO/γ-Al(2)O(3) catalyst had excellent catalytic activity in treating azo dyes. Almost 99% of color and 70% of TOC were removed in 2h. The high removal extent of color and TOC indicated that the CWAO obtained perfect decomposition for pollutants. The degradation pathway of azo dyes was analyzed by UV-Vis, FTIR and MS. According to the examined results, the hydroxyl ((·)OH) radicals induced strong oxidizing effects in the target solution and destroyed the chromophoric groups of azo-benzene conjugated of the molecular structure. Considering characteristics of the dye structure, the azo bond (-N=N-) would first be attacked by the hydroxyl radical and other free radicals. With the continuous oxidization and the long reaction time at high temperature, these intermediates could be oxidized to the final oxidation products, such as water and carbon dioxide. PMID:22795071

  9. Novel Na2Mo4O13/α-MoO3 hybrid material as highly efficient CWAO catalyst for dye degradation at ambient conditions

    PubMed Central

    Zhang, Zhang; Yang, Ruoyan; Gao, Yanshan; Zhao, Yufei; Wang, Junyang; Huang, Liang; Guo, Jiang; Zhou, Tuantuan; Lu, Peng; Guo, Zhanhu; Wang, Qiang

    2014-01-01

    We report a novel hybrid material Na2Mo4O13/α-MoO3 as highly efficient catalytic wet air oxidation (CWAO) catalyst, which showed the highest ever activity at room temperature and atmosphere pressure for the degradation of cationic red GTL. SEM and TEM analyses indicated that this hybrid catalyst has bamboo-shaped nanofiber morphology. In view of practical applications, the influence of some key parameters including operation temperature, catalyst calcination temperature, and the volume of dye wastewater have been optimized. The mechanism for the superior catalytic performance was investigated. XRD, XPS, and ESR suggested the Na2Mo4O13/α-MoO3 hybrid catalyst possesses more O2− ions in the oxygen deficient regions than neat α-MoO3, promoting the formation of active ·OH radicals and resulting in a higher activity. Considering the facile preparation and its superior activity, this novel catalyst is promising for practical dye wastewater treatment. PMID:25348943

  10. Unexpected toxicity to aquatic organisms of some aqueous bisphenol A samples treated by advanced oxidation processes.

    PubMed

    Tišler, Tatjana; Erjavec, Boštjan; Kaplan, Renata; Şenilă, Marin; Pintar, Albin

    2015-01-01

    In this study, photocatalytic and catalytic wet-air oxidation (CWAO) processes were used to examine removal efficiency of bisphenol A from aqueous samples over several titanate nanotube-based catalysts. Unexpected toxicity of bisphenol A (BPA) samples treated by means of the CWAO process to some tested species was determined. In addition, the CWAO effluent was recycled five- or 10-fold in order to increase the number of interactions between the liquid phase and catalyst. Consequently, the inductively coupled plasma mass spectrometry (ICP-MS) analysis indicated higher concentrations of some toxic metals like chromium, nickel, molybdenum, silver, and zinc in the recycled samples in comparison to both the single-pass sample and the photocatalytically treated solution. The highest toxicity of five- and 10-fold recycled solutions in the CWAO process was observed in water fleas, which could be correlated to high concentrations of chromium, nickel, and silver detected in tested samples. The obtained results clearly demonstrated that aqueous samples treated by means of advanced oxidation processes should always be analyzed using (i) chemical analyses to assess removal of BPA and total organic carbon from treated aqueous samples, as well as (ii) a battery of aquatic organisms from different taxonomic groups to determine possible toxicity. PMID:26114268

  11. ZnO/MoO 3 mixed oxide nanotube: A highly efficient and stable catalyst for degradation of dye by air under room conditions

    NASA Astrophysics Data System (ADS)

    Huang, Jiguo; Wang, Xiaohong; Li, Sen; Wang, Yu

    2010-10-01

    As a continuation of our work to develop catalysts with high activity for catalytic air wet oxidation process under mild conditions, degradation of wastewater containing 0.3 g/L Safranin-T (ST) by air oxidation over ZnO/MoO 3 nanotube catalyst was studied. It was found the decolorization efficiency and the chemical oxygen demand (COD) removal of ST reached above 98% and 95%, respectively, within 18 min at room temperature and atmospheric pressure. And the organic pollutants were totally mineralized to simple inorganic species such as HCO 3-, Cl - and NO 3-, while the total organic carbon (TOC) decreased 99.3%. The structure and morphology of the catalyst after ten cycling runs showed that the catalyst was stable under such operating condition and the leaching test showed negligible leaching effect. This ZnO/MoO 3 nanotube is proved to be an active and stable heterogeneous catalyst in CWAO of ST under extremely mild conditions.

  12. Toxicity to Daphnia magna and Vibrio fischeri of Kraft bleach plant effluents treated by catalytic wet-air oxidation.

    PubMed

    Pintar, Albin; Besson, Michèle; Gallezot, Pierre; Gibert, Janine; Martin, Dominique

    2004-01-01

    Two Kraft-pulp bleaching effluents from a sequence of treatments which include chlorine dioxide and caustic soda were treated by catalytic wet-air oxidation (CWAO) at T=463 K in trickle-bed and batch-recycle reactors packed with either TiO2 extrudates or Ru(3 wt%)/TiO2 catalyst. Chemical analyses (TOC removal, color, HPLC) and bioassays (48-h and 30-min acute toxicity tests using Daphnia magna and Vibrio fischeri, respectively) were used to get information about the toxicity impact of the starting effluents and of the treated solutions. Under the operating conditions, complex organic compounds are mostly oxidized into carbon dioxide and water, along with short-chain carboxylic acids. Bioassays were found as a complement to chemical analyses for ensuring the toxicological impact on the ecosystem. In spite of a large decrease of TOC, the solutions of end products were all more toxic to Daphnia magna than the starting effluents by factors ranging from 2 to 33. This observation is attributed to the synergistic effects of acetic acid and salts present in the solutions. On the other hand, toxicity reduction with respect to Vibrio fischeri was achieved: detoxification factors greater than unity were measured for end-product solutions treated in the presence of the Ru(3 wt%)/TiO2 catalyst, suggesting the absence of cumulative effect for this bacteria, or a lower sensitivity to the organic acids and salts. Bleach plant effluents treated by the CWAO process over the Ru/TiO2 catalyst were completely biodegradable. PMID:14675640

  13. Comparative study of supported CuOx and MnOx catalysts for the catalytic wet air oxidation of β-naphthol

    NASA Astrophysics Data System (ADS)

    Liu, Jie; Yu, Chaoying; Zhao, Peiqing; Chen, Gexin

    2012-09-01

    MnOx/nano-TiO2, MnOx/Al2O3-TiO2 (Al-Ti), CuOx/nano-TiO2 and CuOx/Al-Ti were prepared and their application in catalytic wet air oxidation (CWAO) of β-naphthol were investigated. The catalysts had been characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and temperature-programmed reduction (TPR) measurements. Phases of CuO, Cu2O, CuAl2O4, MnO2 and Mn2O3 could be found on the surface of the aforementioned catalysts. Significant differences in activities were observed among the prepared catalysts. Compared to CuOx/nano-TiO2, the combined action of highly dispersed CuO as well as CuAl2O4 of CuOx/Al-Ti helped to achieve higher activity for the CWAO of β-naphthol, while the Cu2O component lead to lower efficiency of CuOx/nano-TiO2. On the surface of MnOx/nano-TiO2, both the larger amount of highly dispersed MnO2 and the stronger electron transfer between MnO2 and Mn2O3 were helpful to promote the activity for the degradation of β-naphthol. However, the higher amount of bulk MnO2 and the weaker electron transfer for MnOx/Al-Ti were unfavorable to increase its efficiency. Among the four catalysts as-prepared, MnOx/nano-TiO2 was identified the highest activity with 93.7% COD removal.

  14. Catalytic behaviour and copper leaching of Cu0.10Zn0.90Al1.90Fe0.10O4 spinel for catalytic wet air oxidation of phenol.

    PubMed

    Xu, Aihua; Sun, Chenglin

    2012-06-01

    A Cu0.10Zn0.90Al1.90Fe0.10O4 spinel catalyst prepared by the sol-gel method was tested for catalytic wet air oxidation (CWAO) of phenol. The catalyst showed high activity for phenol degradation. During successive test at 170 degrees C, 100% phenol conversion and 95% chemical oxygen demand (COD) removal were observed. Results from scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) indicated that the catalyst structure remained unchanged during reaction. From the analysis of temperature programmed reduction (TPR), diffuse reflectance UV-Vis spectra (DR UV-Vis) and activity assay at basic solution pH, it can be suggested that the highly dispersed copper ions on the catalyst surface were almost completely dissolved into the reaction solution, whereas the tetra-coordinated copper ions were not only stable against leaching but also active towards phenol degradation. PMID:22856307

  15. Al 2O 3 supported Ru catalysts prepared by thermolysis of Ru 3(CO) 12 for catalytic wet air oxidation

    NASA Astrophysics Data System (ADS)

    Yu, Chaoying; Zhao, Peiqing; Chen, Gexin; Hu, Bin

    2011-06-01

    Low loading catalysts Ru/γ-Al 2O 3 and Ru-Ce/γ-Al 2O 3 were prepared by thermolysis of Ru 3(CO) 12 on γ-Al 2O 3. The catalysts were characterized by XPS, XRD and SEM. Two new Ru species (Ru A and Ru B) were detected during the Ru 3(CO) 12 decomposition process due to chemical interaction with the active OH groups on the surface of Al 2O 3 support, and the reduction of them can lead to more dispersed metallic phases. The sample was completely decomposed at 673 K in H 2, and RuO 2 was formed with minor amounts of Ru 0. When the temperature was increased to 773 K to heat the sample, the ratio of Ru 0 to RuO 2 increased. However, after the addition of CeO 2, only RuO 2 was detected on surface. The catalysts exhibited high activities in Catalytic Wet Air Oxidation (CWAO) of different organic compounds at high concentration such as isopropyl alcohol, phenol, acetic acids and N,N-dimethylformamide, which is attributed to the better dispersion of Ru particles and the addition of CeO 2 further enhanced number of effectively active sites on the cluster-derived catalyst surface.

  16. DESTRUCTION OF AIR EMISSIONS USING CATALYTIC OXIDATION

    EPA Science Inventory

    The paper discusses key emission stream characteristics and hazardous air pollutant (HAP) characteristics that affect the applicability of catalytic oxidation as an air pollution control technique in which volatile organic compounds (VOCs) and vapor-phase air toxics in an air emi...

  17. Degradation of phenol via wet-air oxidation over CuO/CeO2-ZrO2 nanocatalyst synthesized employing ultrasound energy: physicochemical characterization and catalytic performance.

    PubMed

    Parvas, Mohsen; Haghighi, Mohammad; Allahyari, Somaiyeh

    2014-01-01

    Catalytic wet air oxidation (CWAO) of phenol was carried out under atmospheric pressure of oxygen at 160 degrees C in a stirred batch reactor over copper catalysts supported by CeO2-ZrO2. The copper with different loadings were impregnated over the composite support by a sonication process. The catalysts were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy dispersive X-ray analysis (EDX), Brunauer-Emmett-Teller (BET) specific surface area and Fourier-transformed infrared analyses. Characteristic peaks attributed to copper were not found in XRD patterns even at high loadings, but based on EDX results, the existence of copper particles was confirmed. It means that sonochemical synthesis method even at high loadings produced small copper particles with low crystallinity and excellent dispersion over the CeO2-ZrO2 composite. FESEM micrographs indicated just slight enhancement in particle size at high loadings of Cu. Blank CWAO experiments illustrated low conversion of phenol using bare CeO2-ZrO2 support. Although some agglomeration of particles was found at high loadings of copper but owning to the fact that almost all ZrO2 particles incorporated into the CeO2 lattice at high contents of Cu, catalyst activity not only did not decrease but also the phenol conversion reached to the higher values. The optimal catalyst loading for phenol degradation was found to be 9 g/l. Complete conversion of phenol was achieved using CuO/CeO2-ZrO2 in 9 g/l catalyst loading with initial phenol concentration of 1000 ppm after 3 h of reaction. PMID:24701909

  18. Carbon and nitrogen removal from glucose-glycine melanoidins solution as a model of distillery wastewater by catalytic wet air oxidation.

    PubMed

    Phuong Thu, Le; Michèle, Besson

    2016-06-01

    Sugarcane molasses distillery wastewater contains melanoidins, which are dark brown recalcitrant nitrogenous polymer compounds. Studies were carried out in batch mode to evaluate Pt and Ru supported catalysts in the Catalytic Wet Air Oxidation (CWAO) process of a synthetic melanoidins solution, prepared by stoichiometric reaction of glucose with glycine. The addition of a catalyst slightly improved TOC removal compared with the non-catalytic reaction, and especially promoted the conversion of ammonium produced from organically-bound nitrogen in melanoidins to molecular nitrogen and nitrate. The selectivity to N2 attained 89% in the presence of the Pt catalysts in the reaction conditions used (TOC=2200mgL(-1), TN=280mgL(-1), 0.5g catalyst loaded with 3% metal, 210°C, 70bar total air pressure). To avoid leaching of the active metal by organically-bound nitrogen, the reaction was very efficiently performed in a two-step reaction consisting in WAO to convert nitrogen into ammonium, before the introduction of a catalyst. PMID:26900982

  19. Oxidative Stress and Air Pollution Exposure

    PubMed Central

    Lodovici, Maura; Bigagli, Elisabetta

    2011-01-01

    Air pollution is associated with increased cardiovascular and pulmonary morbidity and mortality. The mechanisms of air pollution-induced health effects involve oxidative stress and inflammation. As a matter of fact, particulate matter (PM), especially fine (PM2.5, PM < 2.5 μm) and ultrafine (PM0.1, PM < 0.1 μm) particles, ozone, nitrogen oxides, and transition metals, are potent oxidants or able to generate reactive oxygen species (ROS). Oxidative stress can trigger redox-sensitive pathways that lead to different biological processes such as inflammation and cell death. However, it does appear that the susceptibility of target organ to oxidative injury also depends upon its ability to upregulate protective scavenging systems. As vehicular traffic is known to importantly contribute to PM exposure, its intensity and quality must be strongly relevant determinants of the qualitative characteristics of PM spread in the atmosphere. Change in the composition of this PM is likely to modify its health impact. PMID:21860622

  20. Nitric oxide flow tagging in unseeded air.

    PubMed

    Dam, N; Klein-Douwel, R J; Sijtsema, N M; Meulen, J J

    2001-01-01

    A scheme for molecular tagging velocimetry is presented that can be used in air flows without any kind of seeding. The method is based on the local and instantaneous creation of nitric oxide (NO) molecules from N(2) and O(2) in the waist region of a focused ArF excimer laser beam. This NO distribution is advected by the flow and can be visualized any time later by laser-induced fluorescence in the gamma bands. The creation of NO is confirmed by use of an excitation spectrum. Two examples of the application of the new scheme for air-flow velocimetry are given in which single laser pulses are used for creation and visualization of NO. PMID:18033499

  1. Specific features of aluminum nanoparticle water and wet air oxidation

    SciTech Connect

    Lozhkomoev, Aleksandr S. Glazkova, Elena A. Svarovskaya, Natalia V. Bakina, Olga V. Kazantsev, Sergey O. Lerner, Marat I.

    2015-10-27

    The oxidation processes of the electrically exploded aluminum nanopowders in water and in wet air are examined in the paper. The morphology of the intermediate reaction products of aluminum oxidation has been studied using the transmission electron microscopy. It was shown that the aluminum nanopowder water oxidation causes the formation of the hollow spheres with mesoporous boehmite nanosheets coating. The wedge-like bayerite particles are formed during aluminum nanopowder wet air oxidation.

  2. Specific features of aluminum nanoparticle water and wet air oxidation

    NASA Astrophysics Data System (ADS)

    Lozhkomoev, Aleksandr S.; Glazkova, Elena A.; Svarovskaya, Natalia V.; Bakina, Olga V.; Kazantsev, Sergey O.; Lerner, Marat I.

    2015-10-01

    The oxidation processes of the electrically exploded aluminum nanopowders in water and in wet air are examined in the paper. The morphology of the intermediate reaction products of aluminum oxidation has been studied using the transmission electron microscopy. It was shown that the aluminum nanopowder water oxidation causes the formation of the hollow spheres with mesoporous boehmite nanosheets coating. The wedge-like bayerite particles are formed during aluminum nanopowder wet air oxidation.

  3. ANALYSIS OF MODIFIED WET-AIR OXIDATION FOR SOIL DETOXIFICATION

    EPA Science Inventory

    The report presents the results of research on wet-air oxidation as a method for the destruction of hazardous wastes. For organics in the presence of large amounts of water, the water need not be vaporized during wet-air oxidation, an attractive characteristic for energy conserva...

  4. AIR QUALITY CRITERIA FOR OZONE AND RELATED PHOTOCHEMICAL OXIDANTS

    EPA Science Inventory

    The Clean Air Act requires periodic (5-year) update revision of criteria and National Ambient Air Quality Standards (NAAQS) for Ozone. The previous revision of the criteria contained in the Air Quality Criteria Document (AQCD) for Ozone and Related Photochemical Oxidants was co...

  5. Oxide modified air electrode surface for high temperature electrochemical cells

    DOEpatents

    Singh, Prabhakar; Ruka, Roswell J.

    1992-01-01

    An electrochemical cell is made having a porous cermet electrode (16) and a porous lanthanum manganite electrode (14), with solid oxide electrolyte (15) between them, where the lanthanum manganite surface next to the electrolyte contains a thin discontinuous layer of high surface area cerium oxide and/or praseodymium oxide, preferably as discrete particles (30) in contact with the air electrode and electrolyte.

  6. Air pollution and circulating biomarkers of oxidative stress

    PubMed Central

    Staimer, Norbert; Vaziri, Nosratola D.

    2013-01-01

    Chemical components of air pollutant exposures that induce oxidative stress and subsequent inflammation may be partly responsible for associations of cardiovascular morbidity and mortality with airborne particulate matter and combustion-related pollutant gasses. However, epidemiologic evidence regarding this is limited. An exposure-assessment approach is to measure the oxidative potential of particle mixtures because it is likely that hundreds of correlated chemicals are involved in overall effects of air pollution on health. Oxidative potential likely depends on particle composition and size distribution, especially ultrafine particle concentration, and on transition metals and certain semivolatile and volatile organic chemicals. For health effects, measuring systemic oxidative stress in the blood is one feasible approach, but there is no universal biomarker of oxidative stress and there are many potential target molecules (lipids, proteins, DNA, nitric oxide, etc.), which may be more or less suitable for specific study goals. Concurrent with the measurement of oxidative stress, it is important to measure gene and/or protein expression of endogenous antioxidant enzymes because they can modify relations between oxidative stress biomarkers and air pollutants. Conversely, the expression and activities of these enzymes are modified by oxidative stress. This interplay will likely determine the observed effects of air pollutants on systemic inflammatory and thrombotic mediators and related clinical outcomes. Studies are needed to assess the reliability and validity of oxidative stress biomarkers, evaluate differences in associations between oxidative stress biomarkers and various pollutant measurements (mass, chemical components, and oxidative potential), and evaluate impacts of antioxidant responses on these relations. PMID:23626660

  7. Wet-air oxidation cleans up black wastewater

    SciTech Connect

    Not Available

    1993-09-01

    Sterling Organics produces the analgesic paracetamol (acetaminophen) at its Dudley, England, plant. The wastewater from the batch process contains intermediates such as para-aminophenol (PAP) and byproducts such as thiosulfates, sulfites and sulfides. To stay ahead of increasingly strict environmental legislation, Sterling Organics installed a wet-air oxidation system at the Dudley facility in August 1992. The system is made by Zimpro Environmental Inc. (Rothschild, Wis.). Zimpro's wet-air oxidation system finds a way around the limitations of purely chemical or physical processes. In the process, compressed air at elevated temperature and pressure oxidizes the process intermediates and byproducts and removes the color from the wastewater.

  8. NEXAFS Study of Air Oxidation for Mg Nanoparticle Thin Film

    NASA Astrophysics Data System (ADS)

    Ogawa, S.; Murakami, S.; Shirai, K.; Nakanishi, K.; Ohta, T.; Yagi, S.

    2013-03-01

    The air oxidation reaction of Mg nanoparticle thin film has been investigated by Mg K-edge NEXAFS technique. It is revealed that MgO is formed on the Mg nanoparticle surfaces at the early stage of the air oxidation for Mg nanoparticle thin film. The simulation of NEXAFS spectrum using standard spectra indicates the existence of complex magnesium carbonates (x(MgCO3).yMg(OH2).z(H2O)) in addition to MgO at the early stage of the air oxidation.

  9. Air Quality Criteria for Sulfur Oxides.

    ERIC Educational Resources Information Center

    National Air Pollution Control Administration (DHEW), Washington, DC.

    Included is a literature review which comprehensively discusses knowledge of the sulfur oxides commonly found in the atmosphere. The subject content is represented by the 10 chapter titles: Physical and Chemical Properties and the Atmospheric Reactions of the Oxides of Sulfur; Sources and Methods of Measurements of Sulfur Oxides in the Atmosphere;…

  10. OXIDANT AIR POLLUTION AND WORK PERFORMANCE OF CITRUS HARVEST LABOR

    EPA Science Inventory

    The project assesses the effect of photochemical oxidants on the work performance of twelve individual citrus pickers in the South Coast Air Basin of southern California. A model of the picker's decision problem is constructed in which oxidants influence the individual's picking ...

  11. The Oxides of Nitrogen in Air Pollution.

    ERIC Educational Resources Information Center

    California State Air Resources Board, Sacramento.

    Research on the health effects of oxides of nitrogen and on the role of oxides of nitrogen in producing photochemical smog effects is presented in this report. Prepared by the California State Department of Public Health at the request of the State Legislature, it gives a comprehensive review of available information, as well as the need for air…

  12. AIR POLLUTION, OXIDATIVE STRESS AND NEUROTOXICITY.

    EPA Science Inventory

    Increased incidents of classic and variant forms of neurodegenerative diseases suggest that environmental chemicals and susceptibility factors (e.g., genetics, diseased states, obesity, etc.) may be contributory. Particulate matter (PM) is a type of air pollution that is associat...

  13. Lithium oxides precipitation in nonaqueous Li-air batteries.

    PubMed

    Hou, Junbo; Yang, Min; Ellis, Michael W; Moore, Robert B; Yi, Baolian

    2012-10-21

    Lithium-air/oxygen battery is a rising star in the field of electrochemical energy storage as a promising alternative to lithium ion batteries. Nevertheless, this alluring system is still at its infant stage, and the breakthrough of lithium-air batteries into the energy market is currently constrained by a combination of scientific and technical challenges. Targeting at the air electrode in nonaqueous lithium-air batteries, this review attempts to summarize the knowledge about the fundamentals related to lithium oxides precipitation, which has been one of the vital and attractive aspects of the research communities of science and technology. PMID:22968061

  14. Effect of fuel/air nonuniformity on nitric oxide emissions

    NASA Technical Reports Server (NTRS)

    Lyons, V. J.

    1979-01-01

    A flame tube combustor holding jet A fuel was used in experiments performed at a pressure of .3 Mpa and a reference velocity of 25 meters/second for three inlet air temperatures of 600, 700, and 800 K. The gas sample measurements were taken at locations 18 cm and 48 cm downstream of the perforated plate flameholder. Nonuniform fuel/air profiles were produced using a fuel injector by separately fueling the inner five fuel tubes and the outer ring of twelve fuel tubes. Six fuel/air profiles were produced for nominal overall equivalence ratios of .5 and .6. An example of three of three of these profiles and their resultant nitric oxide NOx emissions are presented. The uniform fuel/air profile cases produced uniform and relatively low profile levels. When the profiles were either center-peaked or edge-peaked, the overall mass-weighted nitric oxide levels increased.

  15. Practical Aspects for Characterizing Air Oxidation of Graphite

    SciTech Connect

    Contescu, Cristian I; Azad, Samina; Miller, Doug; Lance, Michael J; Baker, Frederick S; Burchell, Timothy D

    2008-01-01

    The efforts for designing of a meaningful and acceptable standard test method for characterization of kinetic parameters of air oxidation of graphite helped identify several practical issues that must be considered for the development of such a test. Using standard size (and shape) specimens, large enough in size to accommodate the inherent local microstructure differences between graphite samples, resulted in non-uniform oxidation profiles and preferential binder oxidation; this was not expected based on the linearity of Arrhenius plots and the (large) values of activation energy. It was found that the transition between the regimes 1 and 2 of graphite oxidation occurs gradually, depending both on the oxidation temperature and rate of oxygen supply. Nevertheless, measuring oxidation rates obtained on standard size samples provides a basis for a meaningful comparison among materials, which may serve as much needed information for predictive models.

  16. Oxidation of oleic acid monolayers at air/liquid interfaces

    NASA Astrophysics Data System (ADS)

    Voss, L. F.; Bazerbashi, M. F.; Beekman, C. P.; Hadad, C. M.; Allen, H. C.

    2006-12-01

    Field studies of marine and continental aerosols find that fatty acid films form on aqueous tropospheric aerosols. Oxidation of the acyl chains is thought to be key to aerosol growth. Oxidation of oleic acid monolayers by ozone was studied to understand the fate of fat-coated aerosols from both fresh and salt water sources. Using vibrational sum frequency generation spectroscopy and reflection absorption infrared spectroscopy, we present a molecular-level investigation of fatty acid monolayers at the air-water and air- sodium chloride solution interface and explore reactions with atmospheric oxidants by these model systems. Using sum frequency generation spectroscopy coupled with a Langmuir trough, concurrent spectroscopic and thermodynamic data were collected to obtain a molecular picture of the monolayers. No substantial difference was observed between oxidation of monolayers spread on water and on 0.6 molar sodium chloride solutions. Results indicate that depending on the size of the aerosol and the extent of oxidation, the subsequent oxidation products may not remain at the surface of these films, but instead be dissolved in the aqueous sub-phase of the aerosol particle. Results also indicate that oxidation of oleic acid could produce monolayers containing species that have no oxidized acyl chains.

  17. Oxidation of oleic acid at air/liquid interfaces

    NASA Astrophysics Data System (ADS)

    Voss, Laura F.; Bazerbashi, Mohamad F.; Beekman, Christopher P.; Hadad, Christopher M.; Allen, Heather C.

    2007-03-01

    Oxidation of oleic acid monolayers by ozone was studied to understand the fate of fat-coated aerosols from both freshwater and saltwater sources. Oleic acid monolayers at the air/water interface and at the air/sodium chloride solution interface were investigated using surface-specific, broad-bandwidth, sum frequency generation spectroscopy. Complementary techniques of infrared reflection adsorption spectroscopy and surface pressure measurements taken during monolayer oxidation confirmed the sum frequency results. Using this nonlinear optical technique coupled with a Langmuir trough, concurrent spectroscopic and thermodynamic data were collected to obtain a molecular picture of the monolayers. No substantial difference was observed between oxidation of monolayers spread on water and on 0.6 M sodium chloride solutions. Results indicate that depending on the size of the aerosol and the extent of oxidation, the subsequent oxidation products may not remain at the surface of these films, but instead be dissolved in the aqueous subphase of the aerosol particle. Results also indicate that oxidation of oleic acid could produce monolayers containing species that have no oxidized acyl chains.

  18. Oxidation of oleic acid monolayers at air/liquid interfaces

    NASA Astrophysics Data System (ADS)

    Voss, Laura

    2008-03-01

    Field studies of marine and continental aerosols find that fatty acid films form on aqueous tropospheric aerosols. Oxidation of oleic acid monolayers by ozone was studied to understand the fate of fat-coated aerosols from both fresh and salt water sources. Using vibrational sum frequency generation spectroscopy and reflection absorption infrared spectroscopy, we present a molecular-level investigation of fatty acid monolayers at the air-water and air-sodium chloride solution interface and explore reactions with atmospheric oxidants by these model systems. Coupling sum frequency generation spectroscopy with a Langmuir trough, concurrent spectroscopic and thermodynamic data were collected to obtain a molecular picture of the monolayers. No substantial difference was observed between oxidation of monolayers spread on water and on 0.6 molar sodium chloride solutions. Results indicate that depending on the size of the aerosol and the extent of oxidation, the subsequent oxidation products may not remain at the surface of these films, but instead be dissolved in the aqueous sub-phase of the aerosol particle. Results also indicate that oxidation of oleic acid could produce monolayers containing species that have no oxidized acyl chains.

  19. HOMOGENEOUS AIR OXIDATION OF HYDROCARBONS UTILIZING MN AND CO CATALYSTS

    EPA Science Inventory

    Homogeneous Air Oxidation of Hydrocarbons Utilizing Mn and Co Catalysts

    Thomas M. Becker and Michael A. Gonzalez*, Sustainable Technology Division, Office of Research and Development; United States Environmental Protection Agency, 26 West Martin Luther King Drive, Mail Sto...

  20. AIR QUALITY CRITERIA FOR OXIDES OF NITROGEN (Final, 1982)

    EPA Science Inventory

    This document is an evaluation and assessment of scientific information relative to determining the health and welfare effects associated with exposure to various concentrations of nitrogen oxides in ambient air. The document is not intended as a complete, detailed literature rev...

  1. INTEGRATION OF PHOTOCATALYTIC OXIDATION WITH AIR STRIPPING OF CONTAMINATED AQUIFERS

    EPA Science Inventory

    Bench scale laboratory studies and pilot scale studies in a simulated field-test situation were performed to evaluate the integration of gas-solid ultaviolet (UV) photocatalytic oxidation (PCO) downstream if an air stripper unit as a technology for cost-effectively treating water...

  2. 75 FR 20595 - Review of the Secondary National Ambient Air Quality Standards for Oxides of Nitrogen and Oxides...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-04-20

    ... for Oxides of Nitrogen and Oxides of Sulfur: First External Review Draft (75 FR 11877; March 12, 2010... AGENCY Review of the Secondary National Ambient Air Quality Standards for Oxides of Nitrogen and Oxides... a proposal addressing the nitrogen oxides (NO X ) and sulfur oxides (SO X ) secondary...

  3. Catalytic oxidative desulfurization of liquid hydrocarbon fuels using air

    NASA Astrophysics Data System (ADS)

    Sundararaman, Ramanathan

    Conventional approaches to oxidative desulfurization of liquid hydrocarbons involve use of high-purity, expensive water soluble peroxide for oxidation of sulfur compounds followed by post-treatment for removal of oxidized sulfones by extraction. Both are associated with higher cost due to handling, storage of oxidants and yield loss with extraction and water separation, making the whole process more expensive. This thesis explores an oxidative desulfurization process using air as an oxidant followed by catalytic decomposition of sulfones thereby eliminating the aforementioned issues. Oxidation of sulfur compounds was realized by a two step process in which peroxides were first generated in-situ by catalytic air oxidation, followed by catalytic oxidation of S compounds using the peroxides generated in-situ completing the two step approach. By this technique it was feasible to oxidize over 90% of sulfur compounds present in real jet (520 ppmw S) and diesel (41 ppmw S) fuels. Screening of bulk and supported CuO based catalysts for peroxide generation using model aromatic compound representing diesel fuel showed that bulk CuO catalyst was more effective in producing peroxides with high yield and selectivity. Testing of three real diesel fuels obtained from different sources for air oxidation over bulk CuO catalyst showed different level of effectiveness for generating peroxides in-situ which was consistent with air oxidation of representative model aromatic compounds. Peroxides generated in-situ was then used as an oxidant to oxidize sulfur compounds present in the fuel over MoO3/SiO2 catalyst. 81% selectivity of peroxides for oxidation of sulfur compounds was observed on MoO3/SiO2 catalyst at 40 °C and under similar conditions MoO3/Al2O3 gave only 41% selectivity. This difference in selectivity might be related to the difference in the nature of active sites of MoO3 on SiO2 and Al2O 3 supports as suggested by H2-TPR and XRD analyses. Testing of supported and bulk Mg

  4. Oxidation and Volatilization from Tantalum Alloy During Air Exposure

    SciTech Connect

    Smolik, Galen Richard; Petti, David Andrew; Schuetz, Stanley Thomas

    2000-10-01

    Tantalum alloys are one of the refractory metals with renewed consideration for high temperatures in fusion reactor applications. Tantalum alloys perform well in protective environments but are oxidized readily in gases containing higher oxygen levels. In addition, the radioactive isotope Ta-182 would be produced in tantalum and could be a significant contributor to dose if mobilized. Other isotopes of importance are produced from tungsten and hafnium. Mobilization of activated products during an accident with air ingress is therefore a safety issue. In this study, we measured the extent of oxidation and mobilization from tantalum alloy T-222 oxidized in flowing air between 500 and 1200 degrees C. This alloy nominally contains 10 wt% tungsten, 2.5 wt% hafnium and 0.01 wt% carbon. We found that the mobilization of Ta and Hf was closely linked to the occurrence of oxide spalling. These elements showed no migration from the test chamber. Some W was mobilized by volatilization as evidenced by transport from the chamber. Tungsten volatilization could occur primarily during initial stages of oxidation before the formation of an oxide scale impedes the process. The mobilization of Ta and W are presented in terms of the mass flux (g/m2-h) as a function of test temperature. These measurements along with specific designs, activation calculations, and accident scenarios provide information useful for dose calculations of future fusion devices.

  5. Initial oxidation of brass induced by humidified air

    PubMed Central

    Qiu, Ping; Leygraf, Christofer

    2011-01-01

    Complementary surface and near-surface analytical techniques have been used to explore a brass (Cu–20Zn) surface before, during, and after exposure in air at 90% relative humidity. Volta potential variations along the unexposed surface are attributed to variations in surface composition and resulted in an accelerated localized growth of ZnO and a retarded more uniform growth of an amorphous Cu2O-like oxide. After 3 days the duplex oxide has a total mass of 1.3 μg/cm2, with improved corrosion protective properties compared to the oxides grown on pure Cu or Zn. A schematic model for the duplex oxide growth on brass is presented. PMID:23471205

  6. Initial oxidation of brass induced by humidified air.

    PubMed

    Qiu, Ping; Leygraf, Christofer

    2011-11-15

    Complementary surface and near-surface analytical techniques have been used to explore a brass (Cu-20Zn) surface before, during, and after exposure in air at 90% relative humidity. Volta potential variations along the unexposed surface are attributed to variations in surface composition and resulted in an accelerated localized growth of ZnO and a retarded more uniform growth of an amorphous Cu2O-like oxide. After 3 days the duplex oxide has a total mass of 1.3 μg/cm(2), with improved corrosion protective properties compared to the oxides grown on pure Cu or Zn. A schematic model for the duplex oxide growth on brass is presented. PMID:23471205

  7. Surface-catalyzed air oxidation of hydrazines: Environmental chamber studies

    NASA Technical Reports Server (NTRS)

    Kilduff, Jan E.; Davis, Dennis D.; Koontz, Steven L.

    1988-01-01

    The surface-catalyzed air oxidation reactions of fuel hydrazines were studied in a 6500-liter fluorocarbon-film chamber at 80 to 100 ppm concentrations. First-order rate constants for the reactions catalyzed by aluminum, water-damaged aluminum (Al/Al2O3), stainless steel 304L, galvanized steel and titanium plates with surface areas of 2 to 24 sq m were determined. With 23.8 sq m of Al/Al2O3 the surface-catalyzed air oxidation of hydrazine had a half-life of 2 hours, diimide (N2H2) was observed as an intermediate and traces of ammonia were present in the final product mixture. The Al/Al2O3 catalyzed oxidation of monomethylhydrazine yielded methyldiazine (HN = NCH3) as an intermediate and traces of methanol. Unsymmetrical dimethylhydrazine gave no detectable products. The relative reactivities of hydrazine, MMH and UDMH were 130 : 7.3 : 1.0, respectively. The rate constants for Al/Al2O3-catalyzed oxidation of hydrazine and MMH were proportional to the square of the surface area of the plates. Mechanisms for the surface-catalyzed oxidation of hydrazine and diimide and the formation of ammonia are proposed.

  8. Biodegradation of air-oxidized Illinois No. 6 coal

    SciTech Connect

    Linehan, J.C.; Fredrickson, J.K.; Wilson, B.W.; Bean, R.M.; Stewart, D.L.; Thomas, B.L.; Campbell, J.A.; Franz, J.A.

    1988-09-01

    We have found that Illinois No. 6 coal, after an air-oxidation pretreatment, can be substantially biodegraded by Penicillium sp. to a product largely soluble in dilute base. It is the purpose of this paper to describe the chemical nature of the biotreated Illinois No. 6 coal and to compare it with the corresponding material from leonardite biosolubilization. 12 refs., 7 figs., 3 tabs.

  9. Cyclic Oxidation of High-Temperature Alloy Wires in Air

    NASA Technical Reports Server (NTRS)

    Reigel, Marissa M.

    2004-01-01

    High-temperature alloy wires are proposed for use in seal applications for future re-useable space vehicles. These alloys offer the potential for improved wear resistance of the seals. The wires must withstand the high temperature environments the seals are subjected to as well as maintain their oxidation resistance during the heating and cooling cycles of vehicle re-entry. To model this, the wires were subjected to cyclic oxidation in stagnant air. of this layer formation is dependent on temperature. Slow growing oxides such as chromia and alumina are desirable. Once the oxide is formed it can prevent the metal from further reacting with its environment. Cyclic oxidation models the changes in temperature these wires will undergo in application. Cycling the temperature introduces thermal stresses which can cause the oxide layer to break off. Re-growth of the oxide layer consumes more metal and therefore reduces the properties and durability of the material. were used for cyclic oxidation testing. The baseline material, Haynes 188, has a Co base and is a chromia former while the other two alloys, Kanthal A1 and PM2000, both have a Fe base and are alumina formers. Haynes 188 and Kanthal A1 wires are 250 pm in diameter and PM2000 wires are 150 pm in diameter. The coiled wire has a total surface area of 3 to 5 sq cm. The wires were oxidized for 11 cycles at 1204 C, each cycle containing a 1 hour heating time and a minimum 20 minute cooling time. Weights were taken between cycles. After 11 cycles, one wire of each composition was removed for analysis. The other wire continued testing for 70 cycles. Post-test analysis includes X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and Energy Dispersive Spectroscopy (EDS) for phase identification and morphology.

  10. Air electrode composition for solid oxide fuel cell

    DOEpatents

    Kuo, L.; Ruka, R.J.; Singhal, S.C.

    1999-08-03

    An air electrode composition for a solid oxide fuel cell is disclosed. The air electrode material is based on lanthanum manganite having a perovskite-like crystal structure ABO{sub 3}. The A-site of the air electrode composition comprises a mixed lanthanide in combination with rare earth and alkaline earth dopants. The B-site of the composition comprises Mn in combination with dopants such as Mg, Al, Cr and Ni. The mixed lanthanide comprises La, Ce, Pr and, optionally, Nd. The rare earth A-site dopants preferably comprise La, Nd or a combination thereof, while the alkaline earth A-site dopant preferably comprises Ca. The use of a mixed lanthanide substantially reduces raw material costs in comparison with compositions made from high purity lanthanum starting materials. The amount of the A-site and B-site dopants is controlled in order to provide an air electrode composition having a coefficient of thermal expansion which closely matches that of the other components of the solid oxide fuel cell. 3 figs.

  11. Air electrode composition for solid oxide fuel cell

    DOEpatents

    Kuo, Lewis; Ruka, Roswell J.; Singhal, Subhash C.

    1999-01-01

    An air electrode composition for a solid oxide fuel cell is disclosed. The air electrode material is based on lanthanum manganite having a perovskite-like crystal structure ABO.sub.3. The A-site of the air electrode composition comprises a mixed lanthanide in combination with rare earth and alkaline earth dopants. The B-site of the composition comprises Mn in combination with dopants such as Mg, Al, Cr and Ni. The mixed lanthanide comprises La, Ce, Pr and, optionally, Nd. The rare earth A-site dopants preferably comprise La, Nd or a combination thereof, while the alkaline earth A-site dopant preferably comprises Ca. The use of a mixed lanthanide substantially reduces raw material costs in comparison with compositions made from high purity lanthanum starting materials. The amount of the A-site and B-site dopants is controlled in order to provide an air electrode composition having a coefficient of thermal expansion which closely matches that of the other components of the solid oxide fuel cell.

  12. Prototypical experiments relating to air oxidation of Zircaloy-4 at high temperatures

    NASA Astrophysics Data System (ADS)

    Steinbrück, Martin

    2009-08-01

    The mechanism of the reaction between Zircaloy-4 and air at temperatures from 800 to 1500 °C was studied. Air attack under prototypical conditions with air ingress during a hypothetic severe nuclear reactor accident was investigated. Oxidation in air and in air and nitrogen-containing atmospheres leads to a major degradation of the cladding material. The main mechanism is the formation of zirconium nitride and its re-oxidation. Pre-oxidation in steam prevents air attack as long as the oxide scale is intact. Under steam/oxygen starvation conditions, the oxide scale is reduced and significant external nitride formation takes place. When modeling air ingress in severe accident computer codes, parabolic correlations for oxidation in air may be applied only for high temperatures (>1400 °C) and for pre-oxidized cladding (⩾1100 °C). Under all other conditions, faster, rather linear reaction kinetics should be applied.

  13. Exergy parametric study of carbon monoxide oxidation in moist air

    NASA Astrophysics Data System (ADS)

    Souidi, Ferhat; Benmalek, Toufik; Yesaad, Billel; Baik, Mouloud

    2015-12-01

    This study aims to analyze the oxidation of carbon monoxide in moist air from the second thermodynamic law aspect. A mathematical model of laminar premixed flame in a stagnation point flow has been achieved by numerical solution of the boundary layer equation using a self-made code. The chemical kinetic mechanism for flameless combustion of fuel, which is a mixture of carbon monoxide, oxygen, and water vapor, is modeled by 34 elementary reactions that incorporate (09) nine chemical species: CO, O, CO2, O2, H2O, H, H2, HO2, and OH. The salient point is that for all the parameters we considered, the exergy of the process is completely destroyed by irreversibilities. From the chemical viewpoint, the OH radical plays an essential role in CO oxidation. This latter point has already been mentioned by previous investigators.

  14. 40 CFR 50.17 - National primary ambient air quality standards for sulfur oxides (sulfur dioxide).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... standards for sulfur oxides (sulfur dioxide). 50.17 Section 50.17 Protection of Environment ENVIRONMENTAL....17 National primary ambient air quality standards for sulfur oxides (sulfur dioxide). (a) The level of the national primary 1-hour annual ambient air quality standard for oxides of sulfur is 75...

  15. 40 CFR 50.5 - National secondary ambient air quality standard for sulfur oxides (sulfur dioxide).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... standard for sulfur oxides (sulfur dioxide). 50.5 Section 50.5 Protection of Environment ENVIRONMENTAL....5 National secondary ambient air quality standard for sulfur oxides (sulfur dioxide). (a) The level... than 0.05 ppm shall be rounded up). (b) Sulfur oxides shall be measured in the ambient air as...

  16. 40 CFR 50.4 - National primary ambient air quality standards for sulfur oxides (sulfur dioxide).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... standards for sulfur oxides (sulfur dioxide). 50.4 Section 50.4 Protection of Environment ENVIRONMENTAL....4 National primary ambient air quality standards for sulfur oxides (sulfur dioxide). (a) The level...). (c) Sulfur oxides shall be measured in the ambient air as sulfur dioxide by the reference...

  17. 40 CFR 50.17 - National primary ambient air quality standards for sulfur oxides (sulfur dioxide).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... standards for sulfur oxides (sulfur dioxide). 50.17 Section 50.17 Protection of Environment ENVIRONMENTAL....17 National primary ambient air quality standards for sulfur oxides (sulfur dioxide). (a) The level of the national primary 1-hour annual ambient air quality standard for oxides of sulfur is 75...

  18. 40 CFR 50.17 - National primary ambient air quality standards for sulfur oxides (sulfur dioxide).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... standards for sulfur oxides (sulfur dioxide). 50.17 Section 50.17 Protection of Environment ENVIRONMENTAL....17 National primary ambient air quality standards for sulfur oxides (sulfur dioxide). (a) The level of the national primary 1-hour annual ambient air quality standard for oxides of sulfur is 75...

  19. 40 CFR 50.17 - National primary ambient air quality standards for sulfur oxides (sulfur dioxide).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... standards for sulfur oxides (sulfur dioxide). 50.17 Section 50.17 Protection of Environment ENVIRONMENTAL....17 National primary ambient air quality standards for sulfur oxides (sulfur dioxide). (a) The level of the national primary 1-hour annual ambient air quality standard for oxides of sulfur is 75...

  20. 40 CFR 50.4 - National primary ambient air quality standards for sulfur oxides (sulfur dioxide).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... standards for sulfur oxides (sulfur dioxide). 50.4 Section 50.4 Protection of Environment ENVIRONMENTAL....4 National primary ambient air quality standards for sulfur oxides (sulfur dioxide). (a) The level...). (c) Sulfur oxides shall be measured in the ambient air as sulfur dioxide by the reference...

  1. 40 CFR 50.5 - National secondary ambient air quality standard for sulfur oxides (sulfur dioxide).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... standard for sulfur oxides (sulfur dioxide). 50.5 Section 50.5 Protection of Environment ENVIRONMENTAL....5 National secondary ambient air quality standard for sulfur oxides (sulfur dioxide). (a) The level... than 0.05 ppm shall be rounded up). (b) Sulfur oxides shall be measured in the ambient air as...

  2. 40 CFR 50.5 - National secondary ambient air quality standard for sulfur oxides (sulfur dioxide).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... standard for sulfur oxides (sulfur dioxide). 50.5 Section 50.5 Protection of Environment ENVIRONMENTAL....5 National secondary ambient air quality standard for sulfur oxides (sulfur dioxide). (a) The level... than 0.05 ppm shall be rounded up). (b) Sulfur oxides shall be measured in the ambient air as...

  3. 40 CFR 50.4 - National primary ambient air quality standards for sulfur oxides (sulfur dioxide).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... standards for sulfur oxides (sulfur dioxide). 50.4 Section 50.4 Protection of Environment ENVIRONMENTAL....4 National primary ambient air quality standards for sulfur oxides (sulfur dioxide). (a) The level...). (c) Sulfur oxides shall be measured in the ambient air as sulfur dioxide by the reference...

  4. 40 CFR 50.17 - National primary ambient air quality standards for sulfur oxides (sulfur dioxide).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... standards for sulfur oxides (sulfur dioxide). 50.17 Section 50.17 Protection of Environment ENVIRONMENTAL....17 National primary ambient air quality standards for sulfur oxides (sulfur dioxide). (a) The level of the national primary 1-hour annual ambient air quality standard for oxides of sulfur is 75...

  5. 40 CFR 50.5 - National secondary ambient air quality standard for sulfur oxides (sulfur dioxide).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... standard for sulfur oxides (sulfur dioxide). 50.5 Section 50.5 Protection of Environment ENVIRONMENTAL....5 National secondary ambient air quality standard for sulfur oxides (sulfur dioxide). (a) The level... than 0.05 ppm shall be rounded up). (b) Sulfur oxides shall be measured in the ambient air as...

  6. 40 CFR 50.4 - National primary ambient air quality standards for sulfur oxides (sulfur dioxide).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... standards for sulfur oxides (sulfur dioxide). 50.4 Section 50.4 Protection of Environment ENVIRONMENTAL....4 National primary ambient air quality standards for sulfur oxides (sulfur dioxide). (a) The level...). (c) Sulfur oxides shall be measured in the ambient air as sulfur dioxide by the reference...

  7. USING WET AIR OXIDATION TECHNOLOGY TO DESTROY TETRAPHENYLBORATE

    SciTech Connect

    Adu-Wusu, K; Daniel McCabe, D; Bill Wilmarth, B

    2007-04-04

    A bench-scale feasibility study on the use of a Wet Air Oxidation (WAO) process to destroy a slurry laden with tetraphenylborate (TPB) compounds has been undertaken. WAO is an aqueous phase process in which soluble and/or insoluble waste constituents are oxidized using oxygen or oxygen in air at elevated temperatures and pressures ranging from 150 C and 1 MPa to 320 C and 22 MPa. The products of the reaction are CO{sub 2}, H{sub 2}O, and low molecular weight oxygenated organics (e.g. acetate, oxalate). Test results indicate WAO is a feasible process for destroying TPB, its primary daughter products [triphenylborane (3PB), diphenylborinic acid (2PB), and phenylboronic acid (1PB)], phenol, and most of the biphenyl byproduct. The required conditions are a temperature of 300 C, a reaction time of 3 hours, 1:1 feed slurry dilution with 2M NaOH solution, the addition of CuSO{sub 4}.5H{sub 2}O solution (500 mg/L Cu) as catalyst, and the addition of 2000 mL/L of antifoam. However, for the destruction of TPB, its daughter compounds (3PB, 2PB, and 1PB), and phenol without consideration for biphenyl destruction, less severe conditions (280 C and 1-hour reaction time with similar remaining above conditions) are adequate.

  8. Oxidative Allylic Esterification of Alkenes by Cooperative Selenium-Catalysis Using Air as the Sole Oxidant.

    PubMed

    Ortgies, Stefan; Depken, Christian; Breder, Alexander

    2016-06-17

    A new metal-free catalysis protocol for the oxidative coupling of nonactivated alkenes with simple carboxylic acids has been established. This method is predicated on the cooperative interaction of a diselane and a photoredox catalyst, which allows for the use of ambient air or pure O2 as the terminal oxidant. Under the title conditions, a range of both functionalized and nonfunctionalized alkenes can be readily converted into the corresponding allylic ester products with good yields (up to 89%) and excellent regioselectivity as well as good functional group tolerance. PMID:27257803

  9. Alveolar macrophage cytokine response to air pollution particles: Oxidant mechanisms

    SciTech Connect

    Imrich, Amy; Ning Yaoyu; Lawrence, Joy; Coull, Brent; Gitin, Elena; Knutson, Mitchell; Kobzik, Lester . E-mail: lkobzik@hsph.harvard.edu

    2007-02-01

    Alveolar macrophages (AMs) primed with LPS and treated with concentrated ambient air particles (CAPs) showed enhanced release of tumor necrosis factor (TNF) and provide an in vitro model for the amplified effects of air pollution particles seen in people with preexisting lung disease. To investigate the mechanism(s) by which CAPs mediate TNF release in primed rat AMs, we first tested the effect of a panel of antioxidants. N-Acetyl-L-cysteine (20 mM), dimethyl thiourea (20 mM) and catalase (5 {mu}M) significantly inhibited TNF release by primed AMs incubated with CAPs. Conversely, when LPS-primed AMs were treated with CAPs in the presence of exogenous oxidants (H{sub 2}O{sub 2} generated by glucose oxidase, 10 {mu}M/h), TNF release and cell toxicity was significantly increased. The soluble fraction of CAPs suspensions caused most of the increased bioactivity in the presence of exogenous H{sub 2}O{sub 2}. The metal chelator deferoxamine (DFO) strongly inhibited the interaction of the soluble fraction with H{sub 2}O{sub 2} but had no effect on the bioactivity of the insoluble CAPs fraction. We conclude that CAPs can mediate their effects in primed AMs by acting on oxidant-sensitive cytokine release in at least two distinct ways. In the primed cell, insoluble components of PM mediate enhanced TNF production that is H{sub 2}O{sub 2}-dependent (catalase-sensitive) yet independent of iron (DFO-insensitive). In the presence of exogenous H{sub 2}O{sub 2} released by AMs, PMNs, or other lung cells within an inflamed alveolar milieu, soluble iron released from air particles can also mediate cytokine release and cell toxicity.

  10. Alveolar macrophage cytokine response to air pollution particles: oxidant mechanisms

    PubMed Central

    Imrich, Amy; Ning, YaoYu; Lawrence, Joy; Coull, Brent; Gitin, Elena; Knutson, Mitchell; Kobzik, Lester

    2007-01-01

    Alveolar macrophages (AMs) primed with LPS and treated with concentrated ambient air particles (CAPs) showed enhanced release of tumor necrosis factor (TNF) and provide an in vitro model for the amplified effects of air pollution particles seen in people with preexisting lung disease. To investigate the mechanism(s) by which CAPs mediate TNF release in primed rat AMs, we first tested the effect of a panel of antioxidants. N-acetyl cysteine (20mM), dimethyl thiourea (20 mM) and catalase (5 uM) significantly inhibited TNF release by primed AMs incubated with CAPs. Conversely, when LPS-primed AMs were treated with CAPs in the presence of exogenous oxidants (H2O2 generated by glucose oxidase, 10 uM/hr), TNF release and cell toxicity was significantly increased. The soluble fraction of CAPs suspensions caused most of the increased bioactivity in the presence of exogenous H2O2. The metal chelator deferoxamine (DFO) strongly inhibited the interaction of the soluble fraction with H2O2 but had no effect on the bioactivity of the insoluble CAPs fraction. We conclude that CAPs can mediate their effects in primed AMs by acting on oxidant-sensitive cytokine release in at least two distinct ways. In the primed cell, insoluble components of PM mediate enhanced TNF production that is H2O2-dependent (catalase-sensitive) yet independent of iron (DFO-insensitive). In the presence of exogenous H2O2 released by AMs, PMNs, or other lung cells within an inflamed alveolar milieu, soluble iron released from air particles can also mediate cytokine release and cell toxicity. PMID:17222881

  11. Air Flow and Pressure Drop Measurements Across Porous Oxides

    NASA Technical Reports Server (NTRS)

    Fox, Dennis S.; Cuy, Michael D.; Werner, Roger A.

    2008-01-01

    This report summarizes the results of air flow tests across eight porous, open cell ceramic oxide samples. During ceramic specimen processing, the porosity was formed using the sacrificial template technique, with two different sizes of polystyrene beads used for the template. The samples were initially supplied with thicknesses ranging from 0.14 to 0.20 in. (0.35 to 0.50 cm) and nonuniform backside morphology (some areas dense, some porous). Samples were therefore ground to a thickness of 0.12 to 0.14 in. (0.30 to 0.35 cm) using dry 120 grit SiC paper. Pressure drop versus air flow is reported. Comparisons of samples with thickness variations are made, as are pressure drop estimates. As the density of the ceramic material increases the maximum corrected flow decreases rapidly. Future sample sets should be supplied with samples of similar thickness and having uniform surface morphology. This would allow a more consistent determination of air flow versus processing parameters and the resulting porosity size and distribution.

  12. Composition of air pollution particles modifies oxidative stress in cells, tissues, and living systems

    EPA Science Inventory

    Epidemiological studies demonstrate an association between increased levels of ambient air pollution particles and human morbidity and mortality. Production of oxidants, either directly by the air pollution particles or by the host response to the particles, appears to be fundame...

  13. 40 CFR 50.4 - National primary ambient air quality standards for sulfur oxides (sulfur dioxide).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 2 2010-07-01 2010-07-01 false National primary ambient air quality... PROTECTION AGENCY (CONTINUED) AIR PROGRAMS NATIONAL PRIMARY AND SECONDARY AMBIENT AIR QUALITY STANDARDS § 50.4 National primary ambient air quality standards for sulfur oxides (sulfur dioxide). Link to...

  14. AIR QUALITY CRITERIA FOR PARTICULATE MATTER AND SULFUR OXIDES (Final, 1982)

    EPA Science Inventory

    Particulate matter and sulfur oxides are two of six major air pollutants regulated by National Ambient Air Quality Standards (NAAQS) under the U.S. Clean Air Act. As mandated by the Clean Air Act, the U.S. Environmental Protection Agency (EPA) must periodically review the scienti...

  15. Evaluation of a Combined Ultraviolet Photocatalytic Oxidation(UVPCO)/Chemisorbent Air Cleaner for Indoor Air Applications

    SciTech Connect

    Hodgson, Alfred T.; Destaillats, Hugo; Hotchi, Toshifumi; Fisk,William J.

    2007-02-01

    We previously reported that gas-phase byproducts of incomplete oxidation were generated when a prototype ultraviolet photocatalytic oxidation (UVPCO) air cleaner was operated in the laboratory with indoor-relevant mixtures of VOCs at realistic concentrations. Under these conditions, there was net production of formaldehyde and acetaldehyde, two important indoor air toxicants. Here, we further explore the issue of byproduct generation. Using the same UVPCO air cleaner, we conducted experiments to identify common VOCs that lead to the production of formaldehyde and acetaldehyde and to quantify their production rates. We sought to reduce the production of formaldehyde and acetaldehyde to acceptable levels by employing different chemisorbent scrubbers downstream of the UVPCO device. Additionally, we made preliminary measurements to estimate the capacity and expected lifetime of the chemisorbent media. For most experiments, the system was operated at 680-780 m{sup 3}/h (400-460 cfm). A set of experiments was conducted with common VOCs introduced into the UVPCO device individually and in mixture. Compound conversion efficiencies and the production of formaldehyde and acetaldehyde were determined by comparison of compound concentrations upstream and downstream of the reactor. There was general agreement between compound conversions efficiencies determined individually and in the mixture. This suggests that competition among compounds for active sites on the photocatalyst surface will not limit the performance of the UVPCO device when the total VOC concentration is low. A possible exception was the very volatile alcohols, for which there were some indications of competitive adsorption. The results also showed that formaldehyde was produced from many commonly encountered VOCs, while acetaldehyde was generated by specific VOCs, particularly ethanol. The implication is that formaldehyde concentrations are likely to increase when an effective UVPCO air cleaner is used in

  16. Air trichloroethylene oxidation in a corona plasma-catalytic reactor

    NASA Astrophysics Data System (ADS)

    Masoomi-Godarzi, S.; Ranji-Burachaloo, H.; Khodadadi, A. A.; Vesali-Naseh, M.; Mortazavi, Y.

    2014-08-01

    The oxidative decomposition of trichloroethylene (TCE; 300 ppm) by non-thermal corona plasma was investigated in dry air at atmospheric pressure and room temperature, both in the absence and presence of catalysts including MnOx, CoOx. The catalysts were synthesized by a co-precipitation method. The morphology and structure of the catalysts were characterized by BET surface area measurement and Fourier Transform Infrared (FTIR) methods. Decomposition of TCE and distribution of products were evaluated by a gas chromatograph (GC) and an FTIR. In the absence of the catalyst, TCE removal is increased with increases in the applied voltage and current intensity. Higher TCE removal and CO2 selectivity is observed in presence of the corona and catalysts, as compared to those with the plasma alone. The results show that MnOx and CoOx catalysts can dissociate the in-plasma produced ozone to oxygen radicals, which enhances the TCE decomposition.

  17. Wet air oxidation of solid waste made of polymers

    SciTech Connect

    Krisner, E.; Ambrosio, M.; Massiani, C.

    2000-03-01

    Wet air oxidation was attempted on synthetic (mixture of plastics of various compositions) and natural (cellulose substances) solid polymers. The temperature was maintained at 270 C and the oxygen pressure varied from 0 to 2 MPa (from understoichiometric conditions to oxygen excess). No valorizable compounds were found, even in runs carried out under an oxygen deficit. Suitable conditions for the total destruction of the initial polymers were temperatures above 270 C, an excess of oxygen, and a residence time of less than 1 h. Only such degradable compounds as acetic and benzoic acids are found at low concentrations. Formation of chlorine and gaseous hydrochloric acid can be limited by adding CaCO{sub 3} as a neutralizing agent.

  18. Photocatalyzed oxidation of ethanol and acetaldehyde in humidified air

    SciTech Connect

    Sauer, M.L.; Ollis, D.F.

    1996-02-01

    Photocatalysis is considered as a potential air treatment and purification technology. Photocatalyzed oxidation of ethanol and acetaldehyde in humidified air was carried out to establish a first complete kinetic model for a photocatalyzed multispecies network. Two photocatalysts were examined in a batch, recirculation reactor, near-UV illuminated TiO{sub 2} (anatase) coated (i) on the surface of a nonporous quartz glass plate and (ii) on a porous ceramic honeycomb monolith. The former contained only illuminated (active) surfaces, the latter consisted of substantial {open_quotes}dark{close_quotes} surfaces coated with a thin layer of illuminated (active) catalyst. Ethanol was photooxidized to acetaldehyde and formaldehyde intermediates, and eventually to carbon dioxide and water products. The catalyst and monolith surfaces adsorbed appreciable fractions of the trace ethanol, acetaldehyde, formaldehyde, carbon dioxide and water present. Ethanol, acetaldehyde, and carbon dioxide adsorption isotherms were measured on both catalysts; the formaldehyde adsorption isotherms were assumed identical to those of acetaldehyde. On the fully illuminated glass plate reactor, all four species were accounted for, and closure of a transient carbon mass balance was demonstrated. Completion of a transient carbon mass balance on the monolith reactor required inclusion of additional reaction intermediates (acetic and formic acids), which appear to reversibly accumulate on only the dark surfaces. The ethanol and acetaldehyde photocatalyzed oxidation kinetic networks were modeled using Langmuir-Hinshelwood rate forms combined with adsorption isotherms for reactant, intermediates, and product CO{sub 2}. For both the quartz plate and monolith catalysts, satisfactory kinetic models were developed to predict the entire time course of ethanol and acetaldehyde multicomponent batch conversions. 43 refs., 16 figs.

  19. Air contamination with nitric oxide: effect on exhaled nitric oxide response.

    PubMed

    Therminarias, A; Flore, P; Favre-Juvin, A; Oddou, M F; Delaire, M; Grimbert, F

    1998-03-01

    This study examines the response of exhaled nitric oxide (NO) concentration (ECNO) and quantity of exhaled NO over time (EVNO) in 10 healthy subjects breathing into five polyethylene bags, one in which synthetic air was free of NO and four in which NO was diluted to concentrations of 20 +/- 0.6, 49 +/- 0.8, 98 +/- 2, and 148 +/- 2 ppb, respectively. Each subject was connected to each bag for 10 min at random. Minute ventilation and ECNO were measured continuously, and EVNO was calculated continuously. ECNO and EVNO values were significantly higher for an inhaled NO concentration of 20 ppb than for NO-free air. Above 20 ppb, ECNO and EVNO increased linearly with inhaled NO concentration. It is reasonable to assume that a share of the quantity of inspired NO over time (InspVNO) because of air contamination by pollution is rejected by the ventilatory pathway. Insofar as InspVNO does not affect endogenous production or the metabolic fate of NO in the airway, this share may be estimated as being approximately one third of InspVNO, the remainder being taken by the endogenous pathway. Thus, air contamination by the NO resulting from pollution greatly increases the NO response in exhaled air. PMID:9517592

  20. Increased amount of nitric oxide in exhaled air of asthmatics.

    PubMed

    Alving, K; Weitzberg, E; Lundberg, J M

    1993-10-01

    The presence of nitric oxide (NO) in the exhaled air of humans has recently been described. We wanted to assess at what level exhaled NO originates in normal airways, and to determine whether airway inflammation induces changes in the levels of exhaled NO. Exhaled NO was continuously measured by chemiluminescence technique during normal tidal breathing through the nose or mouth, with a detection limit of 1 part per billion (ppb). Twelve control subjects were compared to eight patients with mild atopic asthma and rhinitis caused by occupational allergen. In control subjects, the major part of NO in exhaled air (up to 30 ppb) seemed to originate in the nasal airways, with only minor contribution from the lower airways and the oral cavity. However, in mild asthmatics, the level of exhaled NO during oral breathing, indicating the involvement of the lower airways, was increased 2-3 fold. Since increased production of NO in the lower airways may involve activated macrophages or neutrophils, we suggest that exhaled NO may be used to instantly monitor ongoing bronchial inflammation, at least when involving inducible NO synthase. PMID:7507065

  1. Treatment of hydraulic fracturing wastewater by wet air oxidation.

    PubMed

    Wang, Wei; Yan, Xiuyi; Zhou, Jinghui; Ma, Jiuli

    2016-01-01

    Wastewater produced by hydraulic fracturing for oil and gas production is characterized by high salinity and high chemical oxygen demand (COD). We applied a combination of flocculation and wet air oxidation technology to optimize the reduction of COD in the treatment of hydraulic fracturing wastewater. The experiments used different values of flocculant, coagulant, and oxidizing agent added to the wastewater, as well as different reaction times and treatment temperatures. The use of flocculants for the pretreatment of fracturing wastewater was shown to improve treatment efficiency. The addition of 500 mg/L of polyaluminum chloride (PAC) and 20 mg/L of anionic polyacrylamide (APAM) during pretreatment resulted in a COD removal ratio of 8.2% and reduced the suspended solid concentration of fracturing wastewater to 150 mg/L. For a solution of pretreated fracturing wastewater with 12 mL of added H2O2, the COD was reduced to 104 mg/L when reacted at 300 °C for 75 min, and reduced to 127 mg/L when reacted at the same temperature for 45 min while using a 1 L autoclave. An optimal combination of these parameters produced treated wastewater that met the GB 8978-1996 'Integrated Wastewater Discharge Standard' level I emission standard. PMID:26942530

  2. 76 FR 46083 - Secondary National Ambient Air Quality Standards for Oxides of Nitrogen and Sulfur

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-01

    ...This proposed rule is being issued as required by a consent decree governing the schedule for completion of this review of the air quality criteria and the secondary national ambient air quality standards (NAAQS) for oxides of nitrogen and oxides of sulfur. Based on its review, EPA proposes to retain the current nitrogen dioxide (NO2) and sulfur dioxide (SO2) secondary......

  3. Oxidation resistance of selected mechanical carbons at 650 deg C in dry flowing air

    NASA Technical Reports Server (NTRS)

    Allen, G. P.; Wisander, D. W.

    1973-01-01

    Oxidation experiments were conducted with several experimental mechanical carbons at 650 C in air flowing at 28 cu cm/sec (STP). Experiments indicate that boron carbide addition and zinc phosphate treatment definitely improved oxidation resistance. Impregnation with coal tar pitch before final graphitization had some beneficial effect on oxidation resistance and it markedly improved flexure strength and hardness. Graphitization temperature alone did not affect oxidation resistance, but with enough added boron carbide the oxidation resistance was increased although the hardness greatly decreased.

  4. The study of leachate treatment by using three advanced oxidation process based wet air oxidation

    PubMed Central

    2013-01-01

    Wet air oxidation is regarded as appropriate options for wastewater treatment with average organic compounds. The general purpose of this research is to determine the efficiency of three wet air oxidation methods, wet oxidation with hydrogen peroxide and absorption with activated carbon in removing organic matter and nitrogenous compounds from Isfahan's urban leachate. A leachate sample with the volume of 1.5 liters entered into a steel reactor with the volume of three liters and was put under a 10-bar pressure, at temperatures of 100, 200, and 300° as well as three retention times of 30, 60, and 90 minutes. The sample was placed at 18 stages of leachate storage ponds in Isfahan Compost Plant with the volume of 20 liters, using three WPO, WAO methods and a combination of WAO/GAC for leachate pre-treatment. Thirty percent of pure oxygen and hydrogen peroxide were applied as oxidation agents. The COD removal efficiency in WAO method is 7.8-33.3%, in BOD is 14.7-50.6%, the maximum removal percentage (efficiency) for NH4-N is 53.3% and for NO3-N is 56.4-73.9%. The removal efficiency of COD and BOD5 is 4.6%-34 and 24%-50 respectively in WPO method. Adding GAC to the reactor, the removal efficiency of all parameters was improved. The maximum removal efficiency was increased 48% for COD, 31%-43.6 for BOD5 by a combinational method, and the ratio of BOD5/COD was also increased to 90%. In this paper, WAO and WPO process was used for Leachate pre-treatment and WAO/GAC combinational process was applied for improving the organic matter removal and leachate treatment; it was also determined that the recent process is much more efficient in removing resistant organic matter. PMID:23369258

  5. 40 CFR 50.5 - National secondary ambient air quality standard for sulfur oxides (sulfur dioxide).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 2 2010-07-01 2010-07-01 false National secondary ambient air quality standard for sulfur oxides (sulfur dioxide). 50.5 Section 50.5 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS NATIONAL PRIMARY AND SECONDARY AMBIENT AIR QUALITY STANDARDS §...

  6. 78 FR 54813 - Approval and Promulgation of Air Quality Implementation Plans; Maine; Oxides of Nitrogen...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-09-06

    ... AGENCY 40 CFR Parts 52 Approval and Promulgation of Air Quality Implementation Plans; Maine; Oxides of... comment period on our proposed Approval and Promulgation of Air Quality Implementation Plans; Maine... materials are available either electronically in www.regulations.gov or in hard copy at Air Quality...

  7. Catalytic air oxidation of biomass-derived carbohydrates to formic acid.

    PubMed

    Li, Jiang; Ding, Dao-Jun; Deng, Li; Guo, Qing-Xiang; Fu, Yao

    2012-07-01

    An efficient catalytic system for biomass oxidation to form formic acid was developed. The conversion of glucose to formic acid can reach up to 52% yield within 3 h when catalyzed by 5 mol% of H(5)PV(2)Mo(10)O(40) at only 373 K using air as the oxidant. Furthermore, the heteropolyacid can be used as a bifunctional catalyst in the conversion of cellulose to formic acid (yield=35%) with air as the oxidant. PMID:22499553

  8. Air feed tube support system for a solid oxide fuel cell generator

    DOEpatents

    Doshi, Vinod B.; Ruka, Roswell J.; Hager, Charles A.

    2002-01-01

    A solid oxide fuel cell generator (12), containing tubular fuel cells (36) with interior air electrodes (18), where a supporting member (82) containing a plurality of holes (26) supports oxidant feed tubes (51), which pass from an oxidant plenum (52") into the center of the fuel cells, through the holes (26) in the supporting member (82), where a compliant gasket (86) around the top of the oxidant feed tubes and on top (28) of the supporting member (82) helps support the oxidant feed tubes and center them within the fuel cells, and loosen the tolerance for centering the air feed tubes.

  9. Laboratory flammability studies of mixtures of hydrogen, nitrous oxide, and air

    SciTech Connect

    Cashdollar, K L; Hertzberg, M; Zlochower, I A; Lucci, C E; Green, G M; Thomas, R A

    1992-06-26

    At the request of the Department of Energy and the Westinghouse Hanford Company, the Bureau of Mines has investigated the flammability of mixtures of hydrogen, nitrous oxide, and air. This work is relevant to the possible hazards of flammable gas generation from nuclear waste tanks at Hanford, WA. The tests were performed in a 120-L spherical chamber under both quiescent and turbulent conditions using both electric spark and pyrotechnic ignition sources. The data reported here for binary mixtures of hydrogen in air generally confirm the data of previous investigators, but they are more comprehensive than those reported previously. The results clarify to a greater extent the complications associated with buoyancy, turbulence, and selective diffusion. The data reported here for ternary mixtures of hydrogen and nitrous oxide in air indicate that small additions of nitrous oxide (relative to the amount of air) have little effect, but that higher concentrations of nitrous oxide (relative to air) significantly increase the explosion hazard.

  10. 40 CFR Appendix S to Part 50 - Interpretation of the Primary National Ambient Air Quality Standards for Oxides of Nitrogen...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

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

  11. 40 CFR Appendix S to Part 50 - Interpretation of the Primary National Ambient Air Quality Standards for Oxides of Nitrogen...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

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

  12. 40 CFR Appendix S to Part 50 - Interpretation of the Primary National Ambient Air Quality Standards for Oxides of Nitrogen...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

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

  13. 40 CFR Appendix S to Part 50 - Interpretation of the Primary National Ambient Air Quality Standards for Oxides of Nitrogen...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

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

  14. Leaf photosynthetic and water-relations responses for 'Valencia' orange trees exposed to oxidant air pollution

    SciTech Connect

    Olszyk, D.M.; Takemoto, B.K.; Poe, M.

    1991-01-01

    Leaf responses were measured to test a hypothesis that reduced photosynthetic capacity and/or altered water relations were associated with reductions in yield for 'Valencia' orange trees (Citrus sinensis (L.), Osbeck) exposed to ambient oxidant air pollution. Exposures were continuous for 4 years to three levels of oxidants (in charcoal-filtered, half-filtered, and non-filtered air). Oxidants had no effect on net leaf photosynthetic rates or on photosynthetic pigment concentrations. A single set of measurements indicated that oxidants increased leaf starch concentrations (24%) prior to flowering, suggesting a change in photosynthate allocation. Leaves exposed to oxidants had small, but consistent, changes in water relations over the summer growing season, compared to trees growing in filtered air. Other changes included decreased stomatal conductance (12%) and transpiration (9%) rates, and increased water pressure potentials (5%). While all responses were subtle, their cumulative impact over 4 years indicated that 'Valencia' orange trees were subject to increased ambient oxidant stress.

  15. Pressurized solid oxide fuel cell integral air accumular containment

    DOEpatents

    Gillett, James E.; Zafred, Paolo R.; Basel, Richard A.

    2004-02-10

    A fuel cell generator apparatus contains at least one fuel cell subassembly module in a module housing, where the housing is surrounded by a pressure vessel such that there is an air accumulator space, where the apparatus is associated with an air compressor of a turbine/generator/air compressor system, where pressurized air from the compressor passes into the space and occupies the space and then flows to the fuel cells in the subassembly module, where the air accumulation space provides an accumulator to control any unreacted fuel gas that might flow from the module.

  16. PHOTOCHEMICAL OXIDANT AIR POLLUTION EFFECTS ON A MIXED CONIFER FOREST FOREST ECOSYSTEM - A PROGRESS REPORT

    EPA Science Inventory

    Since 1972, twelve scientists representing several research disciplines have collaborated in integrated studies to determine the chronic effects of photochemical oxidant air pollutants on a western mixed conifer forest ecosystem. An enormous amount of data has been collected, des...

  17. Reaction rate constant for dry air oxidation of K Basin fuel

    SciTech Connect

    Trimble, D.J.

    1998-04-29

    The rate of oxidation of spent nuclear fuel stored in the K Basin water is an important parameter when assessing the processes and accident scenarios for preparing the fuel for dry storage. The literature provides data and rate laws for the oxidation of unirradiated uranium in various environments. Measurement data for the dry air oxidation of K Basin fuel is compared to the literature data for linear oxidation in dry air. Equations for the correlations and statistical bounds to the K Basin fuel data and the literature data are selected for predicting nominal and bounding rates for the dry air oxidation of the K Basin fuel. These rate equations are intended for use in the Spent Nuclear Fuel Project Technical Data book.

  18. Air Quality Criteria for Ozone and Related Photochemical Oxidants (Second External Review Draft)

    EPA Science Inventory

    This second external review draft of the Air Quality Criteria for Ozone and Related Photochemical Oxidants, Volumes I-III (Ozone Criteria Document) is being released for public comment and for review by EPA's Clean Air Scientific Advisory Committee (CASAC) r...

  19. AIR QUALITY CRITERIA FOR OXIDES OF NITROGEN (External Review Draft, 1991)

    EPA Science Inventory

    The revised air quality criteria document for oxides of nitrogen (NOx) reviews and evaluates the scientific information on the health and welfare effects associated with exposure to concentrations of NO2 found in ambient air. Although the document is not intended to be an exhaust...

  20. Effect of fuel-air-ratio nonuniformity on emissions of nitrogen oxides

    NASA Technical Reports Server (NTRS)

    Lyons, V. J.

    1981-01-01

    The inlet fuel-air ratio nonuniformity is studied to deterine how nitrogen oxide (NOx) emissions are affected. An increase in NOx emissions with increased fuel-air ratio nonuniformity for average equivalence ratios less than 0.7 and a decrease in NOx emissions for average equivalence ratios near stoichiometric is predicted. The degree of uniformityy of fuel-air ratio profiles that is necessary to achieve NOx emissions goals for actual engines that use lean, premixed, prevaporized combustion systems is determined.

  1. DEVELOPMENT OF TRANSITION METAL OXIDE-ZEOLITE CATALYSTS TO CONTROL CHLORINATED VOC AIR EMISSIONS

    EPA Science Inventory

    The paper discusses the development of transition metal oxide (TMO)-zeolite oxidation catalysts to control chlorinated volatile organic compound (CVOC) air emissions. esearch has been initiated to enhance the utility of these catalysts by the development of a sorption-catalyst sy...

  2. Heterogeneous photochemical reactions of a propylene-nitrogen dioxide-metal oxide-dry air system

    NASA Astrophysics Data System (ADS)

    Takeuchi, Koji; Ibusuki, Takashi

    Photochemical reactions of a C 3H 6-NO 2-air system in the presence of metal oxide were investigated. The metal oxides showing strong photooxidation activity were found to be n-type semiconductor oxides with the energy band gap around 3 eV. Formation of cyano-compounds (HCN and CH 3CN) was also observed and the activity can be explained in terms of the adsorptivity of NO onto metal oxides. Coalfired fly ash as a model of mixed metal oxides was also examined and their photocatalytic action was discussed.

  3. AIR QUALITY CRITERIA FOR OXIDES OF NITROGEN (Final, 1993)

    EPA Science Inventory

    This criteria document focuses on a review and assessment of the effects on human health and welfare of the nitrogen oxides, nitric oxide (NO) and nitrogen dioxide (NO2), and the related compounds, nitrites, nitrates, nitrogenous acids, and nitrosamines. Although the emphasis is ...

  4. CONCENTRATED AMBIENT AIR POLLUTION CREATES OXIDATIVE STRESS IN CNS MICROGLIA.

    EPA Science Inventory

    Nanometer size particles carry free radical activity on their surface and can produce oxidative stress (OS)-mediated damage upon impact to target cells. The initiating event of phage cell activation (i.e., the oxidative burst) is unknown, although many proximal events have been i...

  5. Development of a Catalytic Wet Air Oxidation Method to Produce Feedstock Gases from Waste Polymers

    NASA Technical Reports Server (NTRS)

    Kulis, Michael J.; Guerrero-Medina, Karen J.; Hepp, Aloysius F.

    2012-01-01

    Given the high cost of space launch, the repurposing of biological and plastic wastes to reduce the need for logistical support during long distance and long duration space missions has long been recognized as a high priority. Described in this paper are the preliminary efforts to develop a wet air oxidation system in order to produce fuels from waste polymers. Preliminary results of partial oxidation in near supercritical water conditions are presented. Inherent corrosion and salt precipitation are discussed as system design issues for a thorough assessment of a second generation wet air oxidation system. This work is currently being supported by the In-Situ Resource Utilization Project.

  6. Nitric oxide density measurements in air and air/fuel nanosecond pulse discharges by laser induced fluorescence

    NASA Astrophysics Data System (ADS)

    Uddi, M.; Jiang, N.; Adamovich, I. V.; Lempert, W. R.

    2009-04-01

    Laser induced fluorescence is used to measure absolute nitric oxide concentrations in air, methane-air and ethylene-air non-equilibrium plasmas, as a function of time after initiation of a single pulse, 20 kV peak voltage, 25 ns pulse duration discharge. A mixture of NO and nitrogen with known composition (4.18 ppm NO) is used for calibration. Peak NO density in air at 60 Torr, after a single pulse, is ~8 × 1012 cm-3 (~4.14 ppm) occurring at ~250 µs after the pulse, with decay time of ~16.5 ms. Peak NO atom mole fraction in a methane-air mixture with equivalence ratio of phiv = 0.5 is found to be approximately equal to that in air, with approximately the same rise and decay rate. In an ethylene-air mixture (also with equivalence ratio of phiv = 0.5), the rise and decay times are comparable to air and methane-air, but the peak NO concentration is reduced by a factor of approximately 2.5. Spontaneous emission measurements show that excited electronic states N2(C 3Π) and NO(A 2Σ) in air at P = 60 Torr decay within ~20 ns and ~1 µs, respectively. Kinetic modelling calculations incorporating air plasma kinetics complemented with the GRI Mech 3.0 hydrocarbon oxidation mechanism are compared with the experimental data using three different NO production mechanisms. It is found that NO concentration rise after the discharge pulse is much faster than predicted by Zel'dovich mechanism reactions, by two orders of magnitude, but much slower compared with reactions of electronically excited nitrogen atoms and molecules, also by two orders of magnitude. It is concluded that processes involving long lifetime (~100 µs) metastable states, such as N2(X 1Σ,v) and O2(b 1Σ), formed by quenching of the metastable N2(A 3Σ) state by ground electronic state O2, may play a dominant role in NO formation. NO decay, in all cases, is found to be dominated by the reverse Zel'dovich reaction, NO + O → N + O2, as well as by conversion into NO2 in a reaction of NO with ozone.

  7. 40 CFR 50.11 - National primary and secondary ambient air quality standards for oxides of nitrogen (with...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... air quality standards for oxides of nitrogen (with nitrogen dioxide as the indicator). 50.11 Section... quality standards for oxides of nitrogen (with nitrogen dioxide as the indicator). (a) The level of the national primary annual ambient air quality standard for oxides of nitrogen is 53 parts per billion...

  8. 40 CFR 50.11 - National primary and secondary ambient air quality standards for oxides of nitrogen (with...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... air quality standards for oxides of nitrogen (with nitrogen dioxide as the indicator). 50.11 Section... quality standards for oxides of nitrogen (with nitrogen dioxide as the indicator). (a) The level of the national primary annual ambient air quality standard for oxides of nitrogen is 53 parts per billion...

  9. 40 CFR 50.11 - National primary and secondary ambient air quality standards for oxides of nitrogen (with...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... air quality standards for oxides of nitrogen (with nitrogen dioxide as the indicator). 50.11 Section... quality standards for oxides of nitrogen (with nitrogen dioxide as the indicator). (a) The level of the national primary annual ambient air quality standard for oxides of nitrogen is 53 parts per billion...

  10. 40 CFR 50.11 - National primary and secondary ambient air quality standards for oxides of nitrogen (with...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... air quality standards for oxides of nitrogen (with nitrogen dioxide as the indicator). 50.11 Section... quality standards for oxides of nitrogen (with nitrogen dioxide as the indicator). (a) The level of the national primary annual ambient air quality standard for oxides of nitrogen is 53 parts per billion...

  11. Air Oxidation of Activated Carbon to Synthesize a Biomimetic Catalyst for Hydrolysis of Cellulose.

    PubMed

    Shrotri, Abhijit; Kobayashi, Hirokazu; Fukuoka, Atsushi

    2016-06-01

    Oxygenated carbon catalyzes the hydrolysis of cellulose present in lignocellulosic biomass by utilizing the weakly acidic functional groups on its surface. Here we report the synthesis of a biomimetic carbon catalyst by simple and economical air-oxidation of a commercially available activated carbon. Air- oxidation at 450-500 °C introduced 2000-2400 μmol g(-1) of oxygenated functional groups on the material with minor changes in the textural properties. Selectivity towards the formation of carboxylic groups on the catalyst surface increased with the increase in oxidation temperature. The degree of oxidation on carbon catalyst was found to be proportional to its activity for hydrolysis of cellulose. The hydrolysis of eucalyptus in the presence of carbon oxidized at 475 °C afforded glucose yield of 77 % and xylose yield of 67 %. PMID:27115288

  12. A review of wet air oxidation and Thermal Hydrolysis technologies in sludge treatment.

    PubMed

    Hii, Kevin; Baroutian, Saeid; Parthasarathy, Raj; Gapes, Daniel J; Eshtiaghi, Nicky

    2014-03-01

    With rapid world population growth and strict environmental regulations, increasingly large volumes of sludge are being produced in today's wastewater treatment plants (WWTP) with limited disposal routes. Sludge treatment has become an essential process in WWTP, representing 50% of operational costs. Sludge destruction and resource recovery technologies are therefore of great ongoing interest. Hydrothermal processing uses unique characteristics of water at elevated temperatures and pressures to deconstruct organic and inorganic components of sludge. It can be broadly categorized into wet oxidation (oxidative) and thermal hydrolysis (non-oxidative). While wet air oxidation (WAO) can be used for the final sludge destruction and also potentially producing industrially useful by-products such as acetic acid, thermal hydrolysis (TH) is mainly used as a pre-treatment method to improve the efficiency of anaerobic digestion. This paper reviews current hydrothermal technologies, roles of wet air oxidation and thermal hydrolysis in sludge treatment, and challenges faced by these technologies. PMID:24457302

  13. Quantitative Analysis of Major Phytochemicals in Orthodox tea (Camellia sinensis), Oxidized under Compressed Air Environment.

    PubMed

    Panda, Brajesh Kumar; Datta, Ashis Kumar

    2016-04-01

    This study describes major changes in phytochemical composition of orthodox tea (Camellia sinensis var. Assamica) oxidized under compressed air (CA). The experiments for oxidation were conducted under air pressure (101, 202, and 303 kPa) for 150 min. Relative change in the concentrations of caffeine, catechins, theaflavins (TF), and thearubigins (TR) were analyzed. Effect of CA pressure was found to be nonsignificant in regulating caffeine concentration during oxidation. But degradation in different catechins as well as formation of different TF was significantly affected by CA pressure. At high CA pressure, TF showed highest peak value. TR was found to have slower rate of formation during initial phase of oxidation than TF. Even though the rate of TR formation was significantly influenced by CA, a portion of catechins remained unoxidized at end of oxidation. Except caffeine, the percent change in rate of formation or degradation were more prominent at 202 kPa. PMID:26970442

  14. Investigating the air oxidation of V(II) ions in a vanadium redox flow battery

    NASA Astrophysics Data System (ADS)

    Ngamsai, Kittima; Arpornwichanop, Amornchai

    2015-11-01

    The air oxidation of vanadium (V(II)) ions in a negative electrolyte reservoir is a major side reaction in a vanadium redox flow battery (VRB), which leads to electrolyte imbalance and self-discharge of the system during long-term operation. In this study, an 80% charged negative electrolyte solution is employed to investigate the mechanism and influential factors of the reaction in a negative-electrolyte reservoir. The results show that the air oxidation of V(II) ions occurs at the air-electrolyte solution interface area and leads to a concentration gradient of vanadium ions in the electrolyte solution and to the diffusion of V(II) and V(III) ions. The effect of the ratio of the electrolyte volume to the air-electrolyte solution interface area and the concentrations of vanadium and sulfuric acid in an electrolyte solution is investigated. A higher ratio of electrolyte volume to the air-electrolyte solution interface area results in a slower oxidation reaction rate. The high concentrations of vanadium and sulfuric acid solution also retard the air oxidation of V(II) ions. This information can be utilized to design an appropriate electrolyte reservoir for the VRB system and to prepare suitable ingredients for the electrolyte solution.

  15. Influence of fission products on ruthenium oxidation and transport in air ingress nuclear accidents

    NASA Astrophysics Data System (ADS)

    Vér, N.; Matus, L.; Kunstár, M.; Osán, J.; Hózer, Z.; Pintér, A.

    2010-01-01

    In separate effect tests at 1000-1200 °C Ru oxidation rate and content of Ru in escaping air flow have been studied with special emphasis on effects of other fission product elements on the Ru oxidation and transport. The results showed that in the decreasing temperature section (1100-600 °C) most of the RuO3 and RuO4 (≈95%) decomposed and formed RuO2 crystals; while the partial pressure of RuO4 in the escaping air was in the range of 10-6 bar. The re-evaporation of deposited RuO2 resulted in about 10-6 bar partial pressure in the outlet gas as well. Measurements demonstrated the importance of surface quality in the decreasing temperature area on the heterogeneous phase decomposition of ruthenium oxides to RuO2. On the other hand water or molybdenum oxide vapour in air appears to decrease the surface catalyzed decomposition of RuOx to RuO2 and increases RuO4 concentration in the escaping air. High temperature reaction with caesium changed the form of the released ruthenium and caused a time delay in appearance of maximum concentration of ruthenium oxides in the ambient temperature escaping gas, while reaction with barium and rare earth oxides extended Ru escape from the high temperature area.

  16. Air-Impregnated Nanoporous Anodic Aluminum Oxide Layers for Enhancing the Corrosion Resistance of Aluminum.

    PubMed

    Jeong, Chanyoung; Lee, Junghoon; Sheppard, Keith; Choi, Chang-Hwan

    2015-10-13

    Nanoporous anodic aluminum oxide layers were fabricated on aluminum substrates with systematically varied pore diameters (20-80 nm) and oxide thicknesses (150-500 nm) by controlling the anodizing voltage and time and subsequent pore-widening process conditions. The porous nanostructures were then coated with a thin (only a couple of nanometers thick) Teflon film to make the surface hydrophobic and trap air in the pores. The corrosion resistance of the aluminum substrate was evaluated by a potentiodynamic polarization measurement in 3.5 wt % NaCl solution (saltwater). Results showed that the hydrophobic nanoporous anodic aluminum oxide layer significantly enhanced the corrosion resistance of the aluminum substrate compared to a hydrophilic oxide layer of the same nanostructures, to bare (nonanodized) aluminum with only a natural oxide layer on top, and to the latter coated with a thin Teflon film. The hydrophobic nanoporous anodic aluminum oxide layer with the largest pore diameter and the thickest oxide layer (i.e., the maximized air fraction) resulted in the best corrosion resistance with a corrosion inhibition efficiency of up to 99% for up to 7 days. The results demonstrate that the air impregnating the hydrophobic nanopores can effectively inhibit the penetration of corrosive media into the pores, leading to a significant improvement in corrosion resistance. PMID:26393523

  17. Air

    MedlinePlus

    ... do to protect yourself from dirty air . Indoor air pollution and outdoor air pollution Air can be polluted indoors and it can ... this chart to see what things cause indoor air pollution and what things cause outdoor air pollution! Indoor ...

  18. Nano-textured copper oxide nanofibers for efficient air cooling

    NASA Astrophysics Data System (ADS)

    An, Seongpil; Jo, Hong Seok; Al-Deyab, Salem S.; Yarin, Alexander L.; Yoon, Sam S.

    2016-02-01

    Ever decreasing of microelectronics devices is challenged by overheating and demands an increase in heat removal rate. Herein, we fabricated highly efficient heat-removal coatings comprised of copper oxide-plated polymer nanofiber layers (thorny devil nanofibers) with high surface-to-volume ratio, which facilitate heat removal from the underlying hot surfaces. The electroplating time and voltage were optimized to form fiber layers with maximal heat removal rate. The copper oxide nanofibers with the thorny devil morphology yielded a superior cooling rate compared to the pure copper nanofibers with the smooth surface morphology. This superior cooling performance is attributed to the enhanced surface area of the thorny devil nanofibers. These nanofibers were characterized with scanning electron microscopy, X-ray diffraction, atomic force microscopy, and a thermographic camera.

  19. Effect of Gadolinium Doping on the Air Oxidation of Uranium Dioxide

    SciTech Connect

    Scheele, Randall D.; Hanson, Brady D.; Cumblidge, Stephen E.; Jenson, Evan D.; Kozelisky, Anne E.; Sell, Rachel L.; MacFarlan, Paul J.; Snow, Lanee A.

    2004-12-04

    Researchers at the Pacific Northwest National Laboratory (PNNL) investigated the effects of gadolinia concentration on the air oxidization of gadolinia-doped uranium dioxide using thermogravimetry and differential scanning calorimetry to determine if such doping could improve uranium dioxide's stability as a nuclear fuel during potential accident scenarios in a nuclear reactor or during long-term disposal. We undertook this study to determine whether the resistance of the uranium dioxide to oxidation to the orthorhombic U3O8 with its attendant crystal expansion could be prevented by addition of gadolinia. Our studies found that gadolinium has little effect on the thermal initiation of the first step of the reported two-step air oxidation of UO2; however, increasing gadolinia content does stabilize the initial tetragonal or cubic product allowing significant oxidation before the second expansive step to U3O8 begins.

  20. Air oxidation of d-limonene (the citrus solvent) creates potent allergens.

    PubMed

    Karlberg, A T; Magnusson, K; Nilsson, U

    1992-05-01

    Products containing as much as 95% of d-limonene are used for, e.g., degreasing metal before industrial painting and for cleaning assemblies. Experimental studies on the sensitizing potential of limonene show diverging results. In a previous study, we found that the sensitizing potential of d-limonene increased with prolonged air exposure. The aim of this study was to make further chemical analyses, to identify compounds formed by air exposure of d-limonene and to study their allergenic potential. d-limonene was found to be a sensitizer after prolonged exposure to air according to 2 Freund's complete adjuvant test (FCAT) experiments and 1 guinea pig maximization test (GPMT) study. No significant response was obtained to d-limonene not air exposed, even if the animals were sensitized to oxidized d-limonene. 5 main oxidation products of d-limonene were identified. (R)-(-)-carvone and a mixture of cis and trans isomers of (+)-limonene oxide were found to be potent sensitizers, while no significant reactions were obtained in the animals induced with a mixture of cis and trans isomers of (-)-carveol. It can be concluded that air oxidation of d-limonene is essential for its sensitizing potential, and that potent allergens are created. PMID:1395597

  1. Mild and selective vanadium-catalyzed oxidation of benzylic, allylic, and propargylic alcohols using air.

    PubMed

    Hanson, Susan K; Wu, Ruilian; Silks, L A Pete

    2011-04-15

    Transition metal-catalyzed aerobic alcohol oxidation is an attractive method for the synthesis of carbonyl compounds, but most catalytic systems feature precious metals and require pure oxygen. The vanadium complex (HQ)(2)V(V)(O)(O(i)Pr) (2 mol %, HQ = 8-quinolinate) and NEt(3) (10 mol %) catalyze the oxidation of benzylic, allylic, and propargylic alcohols with air. The catalyst can be easily prepared under air using commercially available reagents and is effective for a wide range of primary and secondary alcohols. PMID:21434606

  2. Effects of ambient oxidant air pollution in the San Joaquin Valley on Thompson seedless grapes

    SciTech Connect

    Brewer, R.F.; Ashcroft, R.

    1984-01-01

    Mature Thompson seedless grape vines were enclosed in specially constructed plastic covered chambers supplied with carbon filtered and non-filtered (ambient) air from time of bud break through leaf drop. Effects on vegetative growth and fruiting were determined for three seasons. No effects on fruit production were measured the first season after covering but vegetative growth increased 12% in chambers supplied with filtered air. By the third season fruit yields were 27.5% higher in the filtered as compared with ambient chambers. The only visible symptoms associated with exposure to the oxidants was accelerated senescence which appeared 3 weeks to 1 month earlier on vines receiving ambient or nonfiltered air.

  3. Experimental Validation of Stratified Flow Phenomena, Graphite Oxidation, and Mitigation Strategies of Air Ingress Accidents

    SciTech Connect

    Chang Ho Oh; Eung Soo Kim; Hee Cheon No; Nam Zin Cho

    2008-12-01

    The US Department of Energy is performing research and development (R&D) that focuses on key phenomena that are important during challenging scenarios that may occur in the Next Generation Nuclear Plant (NGNP) Program / GEN-IV Very High Temperature Reactor (VHTR). Phenomena identification and ranking studies (PIRT) to date have identified the air ingress event, following on the heels of a VHTR depressurization, as very important (Schultz et al., 2006). Consequently, the development of advanced air ingress-related models and verification and validation (V&V) are very high priority for the NGNP program. Following a loss of coolant and system depressurization, air will enter the core through the break. Air ingress leads to oxidation of the in-core graphite structure and fuel. The oxidation will accelerate heat-up of the bottom reflector and the reactor core and will cause the release of fission products eventually. The potential collapse of the bottom reflector because of burn-off and the release of CO lead to serious safety problems. For estimation of the proper safety margin we need experimental data and tools, including accurate multi-dimensional thermal-hydraulic and reactor physics models, a burn-off model, and a fracture model. We also need to develop effective strategies to mitigate the effects of oxidation. The results from this research will provide crucial inputs to the INL NGNP/VHTR Methods R&D project. This project is focused on (a) analytical and experimental study of air ingress caused by density-driven, stratified, countercurrent flow, (b) advanced graphite oxidation experiments, (c) experimental study of burn-off in the bottom reflector, (d) structural tests of the burnt-off bottom reflector, (e) implementation of advanced models developed during the previous tasks into the GAMMA code, (f) full air ingress and oxidation mitigation analyses, (g) development of core neutronic models, (h) coupling of the core neutronic and thermal hydraulic models, and (i

  4. Synthesis and characterization of carbon black/manganese oxide air cathodes for zinc-air batteries

    NASA Astrophysics Data System (ADS)

    Li, Po-Chieh; Hu, Chi-Chang; Lee, Tai-Chou; Chang, Wen-Sheng; Wang, Tsin Hai

    2014-12-01

    Due to the poor electric conductivity but the excellent catalytic ability for the oxygen reduction reaction (ORR), manganese dioxide in the α phase (denoted as α-MnO2) anchored onto carbon black powders (XC72) has been synthesized by the reflux method. The specific surface area and electric conductivity of the composites are generally enhanced by increasing the XC72 content while the high XC72 content will induce the formation of MnOOH which shows a worse ORR catalytic ability than α-MnO2. The ORR activity of such air cathodes have been optimized at the XC72/α-MnO2 ratio equal to 1 determined by the thermogravimetric analysis. By using this optimized cathode under the air atmosphere, the quasi-steady-state full-cell discharge voltages are equal to 1.353 and 1.178 V at 2 and 20 mA cm-2, respectively. Due to the usage of ambient air rather than pure oxygen, this Zn-air battery shows a modestly high discharge peak power density (67.51 mW cm-2) meanwhile the power density is equal to 47.22 mW cm-2 and the specific capacity is more than 750 mAh g-1 when this cell is operated at 1 V.

  5. Unusually high soil nitrogen oxide emissions influence air quality in a high-temperature agricultural region

    NASA Astrophysics Data System (ADS)

    Oikawa, P. Y.; Ge, C.; Wang, J.; Eberwein, J. R.; Liang, L. L.; Allsman, L. A.; Grantz, D. A.; Jenerette, G. D.

    2015-11-01

    Fertilized soils have large potential for production of soil nitrogen oxide (NOx=NO+NO2), however these emissions are difficult to predict in high-temperature environments. Understanding these emissions may improve air quality modelling as NOx contributes to formation of tropospheric ozone (O3), a powerful air pollutant. Here we identify the environmental and management factors that regulate soil NOx emissions in a high-temperature agricultural region of California. We also investigate whether soil NOx emissions are capable of influencing regional air quality. We report some of the highest soil NOx emissions ever observed. Emissions vary nonlinearly with fertilization, temperature and soil moisture. We find that a regional air chemistry model often underestimates soil NOx emissions and NOx at the surface and in the troposphere. Adjusting the model to match NOx observations leads to elevated tropospheric O3. Our results suggest management can greatly reduce soil NOx emissions, thereby improving air quality.

  6. Unusually high soil nitrogen oxide emissions influence air quality in a high-temperature agricultural region.

    PubMed

    Oikawa, P Y; Ge, C; Wang, J; Eberwein, J R; Liang, L L; Allsman, L A; Grantz, D A; Jenerette, G D

    2015-01-01

    Fertilized soils have large potential for production of soil nitrogen oxide (NOx=NO+NO2), however these emissions are difficult to predict in high-temperature environments. Understanding these emissions may improve air quality modelling as NOx contributes to formation of tropospheric ozone (O3), a powerful air pollutant. Here we identify the environmental and management factors that regulate soil NOx emissions in a high-temperature agricultural region of California. We also investigate whether soil NOx emissions are capable of influencing regional air quality. We report some of the highest soil NOx emissions ever observed. Emissions vary nonlinearly with fertilization, temperature and soil moisture. We find that a regional air chemistry model often underestimates soil NOx emissions and NOx at the surface and in the troposphere. Adjusting the model to match NOx observations leads to elevated tropospheric O3. Our results suggest management can greatly reduce soil NOx emissions, thereby improving air quality. PMID:26556236

  7. Unusually high soil nitrogen oxide emissions influence air quality in a high-temperature agricultural region

    PubMed Central

    Oikawa, P. Y.; Ge, C.; Wang, J.; Eberwein, J. R.; Liang, L. L.; Allsman, L. A.; Grantz, D. A.; Jenerette, G. D.

    2015-01-01

    Fertilized soils have large potential for production of soil nitrogen oxide (NOx=NO+NO2), however these emissions are difficult to predict in high-temperature environments. Understanding these emissions may improve air quality modelling as NOx contributes to formation of tropospheric ozone (O3), a powerful air pollutant. Here we identify the environmental and management factors that regulate soil NOx emissions in a high-temperature agricultural region of California. We also investigate whether soil NOx emissions are capable of influencing regional air quality. We report some of the highest soil NOx emissions ever observed. Emissions vary nonlinearly with fertilization, temperature and soil moisture. We find that a regional air chemistry model often underestimates soil NOx emissions and NOx at the surface and in the troposphere. Adjusting the model to match NOx observations leads to elevated tropospheric O3. Our results suggest management can greatly reduce soil NOx emissions, thereby improving air quality. PMID:26556236

  8. Soot Surface Oxidation in Laminar Hydrocarbon/Air Diffusion Flames at Atmospheric Pressure. Appendix I

    NASA Technical Reports Server (NTRS)

    Xu, F.; El-Leathy, A. M.; Kim, C. H.; Faeth, G. M.; Yuan, Z.-G. (Technical Monitor); Urban, D. L. (Technical Monitor); Yuan, Z.-G. (Technical Monitor)

    2003-01-01

    Soot surface oxidation was studied experimentally in laminar hydrocarbon/air diffusion flames at atmospheric pressure. Measurements were carried out along the axes of round fuel jets burning in coflowing dry air considering acetylene-nitrogen, ethylene, propyiene-nitrogen, propane and acetylene-benzene-nitrogen in the fuel stream. Measurements were limited to the initial stages of soot oxidation (carbon consumption less than 70%) where soot oxidation occurs at the surface of primary soot particles. The following properties were measured as a function of distance above the burner exit: soot concentrations by deconvoluted laser extinction, soot temperatures by deconvoluted multiline emission, soot structure by thermophoretic sampling and analysis using Transmission Electron Microscopy (TEM), concentrations of major stable gas species (N2, H2O, H2, O2, CO, CO2, CH4, C2H2, C2H6, C3H6, C3H8, and C6H6) by sampling and gas chromatography, concentrations of some radical species (H, OH, O) by deconvoluted Li/LiOH atomic absorption and flow velocities by laser velocimetry. For present test conditions, it was found that soot surface oxidation rates were not affected by fuel type, that direct rates of soot surface oxidation by O2 estimated from Nagle and Strickland-Constable (1962) were small compared to observed soot surface oxidation rates because soot surface oxidation was completed near the flame sheet where O2 concentrations were less than 3% by volume, and that soot surface oxidation rates were described by the OH soot surface oxidation mechanism with a collision efficiency of 0.14 and an uncertainty (95% confidence) of +/- 0.04 when allowing for direct soot surface oxidation by O2, which is in reasonably good agreement with earlier observations of soot surface oxidation rates in both premixed and diffusion flames at atmospheric pressure.

  9. Isothermal and cyclic oxidation of an air plasma-sprayed thermal barrier coating system

    SciTech Connect

    Haynes, J.A.; Ferber, M.K.; Porter, W.D.; Rigney, E.D.

    1996-08-01

    Thermogravimetric methods for evaluating bond coat oxidation in plasma-sprayed thermal barrier coating (TBC) systems were assessed by high-temperature testing of TBC systems with air plasma-sprayed (APS) Ni-22Cr-10Al-1Y bond coatings and yttria-stabilized zirconia top coatings. High-mass thermogravimetric analysis (at 1150{sup degrees}C) was used to measure bond coat oxidation kinetics. Furnace cycling was used to evaluate APS TBC durability. This paper describes the experimental methods and relative oxidation kinetics of the various specimen types. Characterization of the APS TBCs and their reaction products is discussed.

  10. Air-Driven Potassium Iodide-Mediated Oxidative Photocyclization of Stilbene Derivatives.

    PubMed

    Matsushima, Tomoya; Kobayashi, Sayaka; Watanabe, Soichiro

    2016-09-01

    A new method has been developed for the potassium iodide-mediated oxidative photocyclization of stilbene derivatives. Compared with conventional iodine-mediated oxidative photocyclization reactions, this new method requires shorter reaction times and affords cyclized products in yields of 45-97%. This reaction proceeds with a catalytic amount of potassium iodide and works in an air-driven manner without the addition of an external scavenger. The radical-mediated oxidative photocyclization of stilbene derivatives using TEMPO was also investigated. PMID:27508401

  11. Solid oxide fuel cell power plant having a fixed contact oxidation catalyzed section of a multi-section cathode air heat exchanger

    DOEpatents

    Saito, Kazuo; Lin, Yao

    2015-02-17

    The multi-section cathode air heat exchanger (102) includes at least a first heat exchanger section (104), and a fixed contact oxidation catalyzed section (126) secured adjacent each other in a stack association. Cool cathode inlet air flows through cool air channels (110) of the at least first (104) and oxidation catalyzed sections (126). Hot anode exhaust flows through hot air channels (124) of the oxidation catalyzed section (126) and is combusted therein. The combusted anode exhaust then flows through hot air channels (112) of the first section (104) of the cathode air heat exchanger (102). The cool and hot air channels (110, 112) are secured in direct heat exchange relationship with each other so that temperatures of the heat exchanger (102) do not exceed 800.degree. C. to minimize requirements for using expensive, high-temperature alloys.

  12. AIR PARTICULATE POLLUTION EXPOSURE INDUCES SYSTEMIC OXIDATIVE STRESS IN HEALTHY MICE

    EPA Science Inventory

    Air particulate pollution exposure induces systemic oxidative stress in healthy mice

    Elizabeth S Roberts1 and Kevin L Dreher2. 1 College or Veterinary Medicine, NC State University, Raleigh, NC , 2US Environmental Protection Agency, NHEERL, RTP, NC

    Epidemiological s...

  13. IN VITRO CARDIOTOXICITY OF AIR POLLUTION PARTICLES: ROLE OF BIOAVAILABLE CONSTITUENTS, OXIDATIVE STRESS AND TYROSINE PHOSPHORYLATION

    EPA Science Inventory

    IN VITRO CARDIOTOXICITY OF AIR POLLUTION PARTICLES: ROLE OF BIOAVAILABLE CONSTITUENTS, OXIDATIVE STRESS AND TYROSINE PHOSPHORYLATION.

    T. L. Knuckles1 R. Jaskot2, J. Richards2, and K.Dreher2.
    1Department of Molecular and Biomedical Sciences, College of Veterinary Medicin...

  14. PHOTOCHEMICAL OXIDANT AIR POLLUTION EFFECTS ON A MIXED CONIFER FOREST ECOSYSTEM

    EPA Science Inventory

    EPA contract 68-03-2442 provided support for three years of the studies to determine the chronic effects of photochemical oxidant air pollutants on a western mixed conifer forest ecosystem. This report deals with the year 1976-77 and is the final publication on EPA contract 68-03...

  15. COST ANALYSIS OF ACTIVATED CARBON VERSUS PHOTOCATALYTIC OXIDATION FOR REMOVING ORGANIC COMPOUNDS FROM INDOOR AIR

    EPA Science Inventory

    A cost comparison has been conducted of 1 m3/s indoor air cleaners using granular activated carbon (GAC) vs. photocatalytic oxidation (PCO) for treating a steady-state inlet volatile organic compound (VOC) concentration of 0.3 mg/m3. The commercial GAC unit was costed assuming t...

  16. Air Quality Criteria for Ozone and Related Photochemical Oxidants (First External Review Draft)

    EPA Science Inventory

    This first external review draft of the Air Quality Criteria for Ozone and Related Photochemical Oxidants (Ozone Criteria Document) is being released in January 2005 for public comment and for review by EPA's Clean A...

  17. Spectroscopic Studies On Powdered CeNi5 Oxidized In Air

    SciTech Connect

    Coldea, M.; Pacurariu, R.; Pascut, L. G.; Rednic, V.; Neumann, M.

    2007-04-23

    The synthesis, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy. X-ray diffraction (XRD) and transmission electron microscopy (TEM) of Ni isolated single domain particles, obtained from powdered CeNi5 oxidized in air at different temperatures up to 800 deg. C, are reported.

  18. LEAF PHOTOSYNTHETIC AND WATER RELATIONS RESPONSES FOR "VALENCIA" ORANGE TREES EXPOSED TO OXIDANT AIR POLLUTION

    EPA Science Inventory

    Leaf responses were measured to test a hypothesis that reduced photosynthetic capacity and/or altered water relations were associated with reductions in yield for "Valencia" orange trees exposed to ambient oxidant air pollution. xposures were continuous for four years to three le...

  19. OXIDANT AIR POLLUTANT EFFECTS ON A WESTERN CONIFEROUS FOREST ECOSYSTEM: TASK A, PLANNING CONFERENCE

    EPA Science Inventory

    This is a report on a planning conference to develop a protocol for a study on the impact of oxidant air pollution from an urban area on a forest ecosystem and recreational area. The conference was held July 21-23, 1971 at the Arrowhead Conference Center in California to discuss ...

  20. THE EFFECTS OF OXIDANT AIR POLLUTANTS ON SOYBEANS, SNAP BEANS AND POTATOES

    EPA Science Inventory

    During the past 5 years the impact of photochemical oxidants on soybeans and snap beans in Maryland and on potatoes in Virginia and Delaware was assessed with open-top chambers. The mean yields of four selected soybean varieties grown in open-top chambers with carbon-filtered air...

  1. OXIDATION OF CYCLOHEXANE WITH AIR CATALYZED BY A STERICALLY HINDERED IRON (II) COMPLEX

    EPA Science Inventory

    Oxidation of Cyclohexane with Air Catalyzed by a Sterically Hindered Iron(II) Complex.


    Thomas M. Becker, Michael A. Gonzalez*

    United States Environmental Protection Agency; National Risk Management Research Laboratory; Sustainable Technology Division; Clean Pr...

  2. Effects of air oxidation on the dissolution rate of LWR spent fuel

    SciTech Connect

    Gray, W.J.; Thomas, L.E.; Einziger, R.E.

    1993-12-31

    Dissolution rates for air-oxidized spent fuel were measured in flowthrough tests where U concentrations were kept well below the solubility limit. Results from two types of specimens, separated grains and coarse particles, both in oxidized (U{sub 4}O{sub 9+x}) and unoxidized (UO{sub 2}) conditions indicated only minor effects of oxidation on the surface-area-normalized rates. Similar results were obtained for unirradiated specimens in three different oxidation states (UO{sub 2}, U{sub 3}O{sub 7}, and U{sub 3}O{sub 8}). These observations have important practical implications for disposal of spent fuel in a geologic repository as well as implications regarding the oxidative dissolution mechanism of UO{sub 2} fuel.

  3. OXIDANT AIR POLLUTION IN REMOTE FORESTED AREAS OF SOUTHWESTERN VIRGINIA. OXIDANT EFFECT ON EASTERN WHITE PINE

    EPA Science Inventory

    Total oxidants and associated oxidant injury to white pine were determined at three rural sites in Virginia: (1) Salt Pond Mountain, Giles County; (2) Rocky Knob Mountain, Floyd County; and, (3) Shenandoah Valley, Rockingham County, at 945 m, 945 m, and 426 m elevation, respectiv...

  4. Treatment of high-strength industrial wastewater by wet air oxidation--A case study

    SciTech Connect

    Lin, S.H.; Ho, S.J.

    1997-12-31

    Treatment of high concentration chemical wastewater obtained from a petrochemical company by wet air oxidation (WAO) is studied. Experiments were conducted to investigate the effects of the mixer speed, operating pressure, initial pH of wastewater and temperature on the pollutant (chemical oxygen demand or COD) removal. Both air and oxygen were tested to determine their respective effect on the COD removal. Results showed that over 50% of COD removal can be easily realized in an hour of WAO treatment. Also considered in the present study was the catalytic WAO treatment of the high concentration wastewater. Copper sulfate (CuSO{sub 4}), cobalt oxide (Co{sub 2}O{sub 3}) and zinc oxide (ZnO) were employed as the catalysts. The COD removal efficiency of the catalytic WAO process was found to vary significantly with the catalyst utilized with CuSO{sub 4} being the most effective.

  5. Impact of Air Pollutants on Oxidative Stress in Common Autophagy-Mediated Aging Diseases

    PubMed Central

    Numan, Mohamed Saber; Brown, Jacques P.; Michou, Laëtitia

    2015-01-01

    Atmospheric pollution-induced cellular oxidative stress is probably one of the pathogenic mechanisms involved in most of the common autophagy-mediated aging diseases, including neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS), Alzheimer’s, disease, as well as Paget’s disease of bone with or without frontotemporal dementia and inclusion body myopathy. Oxidative stress has serious damaging effects on the cellular contents: DNA, RNA, cellular proteins, and cellular organelles. Autophagy has a pivotal role in recycling these damaged non-functional organelles and misfolded or unfolded proteins. In this paper, we highlight, through a narrative review of the literature, that when autophagy processes are impaired during aging, in presence of cumulative air pollution-induced cellular oxidative stress and due to a direct effect on air pollutant, autophagy-mediated aging diseases may occur. PMID:25690002

  6. INVESTIGATION OF A NOVEL AIR BRAZING COMPOSITION FOR HIGH-TEMPERATURE, OXIDATION-RESISTANT CERAMIC JOINING

    SciTech Connect

    Weil, K. Scott; Hardy, John S.; Darsell, Jens T.

    2004-01-30

    One of the challenges in developing a useful ceramic joining technique is in producing a joint that offers good strength under high temperature and highly oxidizing operating conditions. Unfortunately many of the commercially available active metal ceramic brazing alloys exhibit oxidation behaviors which are unacceptable for use in a high temperature application. We have developed a new approach to ceramic brazing, referred to as air brazing, that employs an oxide wetting agent dissolved in a molten noble metal solvent, in this case CuO in Ag, such that acceptable wetting behavior occurs on a number of ceramic substrates. In an effort to explore how to increase the operating temperature of this type of braze, we have investigated the effect of ternary palladium additions on the wetting characteristics of our standard Ag-CuO air braze composition

  7. Interim results from UO/sub 2/ fuel oxidation tests in air

    SciTech Connect

    Campbell, T.K.; Gilbert, E.R.; Thornhill, C.K.; White, G.D.; Piepel, G.F.; Griffin, C.W.j

    1987-08-01

    An experimental program is being conducted at Pacific Northwest Laboratory (PNL) to extend the characterization of spent fuel oxidation in air. To characterize oxidation behavior of irradiated UO/sub 2/, fuel oxidation tests were performed on declad light-water reactor spent fuel and nonirradited UO/sub 2/ pellets in the temperature range of 135 to 250/sup 0/C. These tests were designed to determine the important independent variables that might affect spent fuel oxidation behavior. The data from this program, when combined with the test results from other programs, will be used to develop recommended spent fuel dry-storage temperature limits in air. This report describes interim test results. The initial PNL investigations of nonirradiated and spent fuels identified the important testing variables as temperature, fuel burnup, radiolysis of the air, fuel microstructure, and moisture in the air. Based on these initial results, a more extensive statistically designed test matrix was developed to study the effects of temperature, burnup, and moisture on the oxidation behavior of spent fuel. Oxidation tests were initiated using both boiling-water reactor and pressurized-water reactor fuels from several different reactors with burnups from 8 to 34 GWd/MTU. A 10/sup 5/ R/h gamma field was applied to the test ovens to simulate dry storage cask conditions. Nonirradiated fuel was included as a control. This report describes experimental results from the initial tests on both the spent and nonirradiated fuels and results to date on the tests in a 10/sup 5/ R/h gamma field. 33 refs., 51 figs., 6 tabs.

  8. Synthesis and characterization of carbon black/manganese oxide air cathodes for zinc-air batteries: Effects of the crystalline structure of manganese oxides

    NASA Astrophysics Data System (ADS)

    Li, Po-Chieh; Hu, Chi-Chang; Noda, Hiroyuki; Habazaki, Hiroki

    2015-12-01

    Manganese oxides (MnOx) in α-, β-, γ-, δ-MnO2 phases, Mn3O4, Mn2O3, and MnOOH are synthesized for systematically comparing their electrocatalytic activity of the oxygen reduction reaction (ORR) in the Zn-air battery application. The optimal MnOx/XC-72 mass ratio for the ORR is equal to 1 and the oxide crystalline structure effect on the ORR is compared. The order of composites with respect to decreasing the ORR activity is: α-MnO2/XC-72 > γ-MnO2/XC-72 > β-MnO2/XC-72 > δ-MnO2/XC-72 > Mn2O3/XC-72 > Mn3O4/XC-72 > MnOOH/XC-72. The textural properties of MnOx are investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), N2 adsorption/desorption isotherms with Brunauer-Emmett-Teller (BET) analysis, X-ray diffraction (XRD), and thermogravimetric analysis (TGA). Electrochemical studies include linear sweep voltammetry (LSV), rotating ring-disk electrode (RRDE) voltammetry, and the full-cell discharge test. The discharge peak power density of Zn-air batteries varies from 61.5 mW cm-2 (α-MnO2/XC-72) to 47.1 mW cm-2 (Mn3O4/XC-72). The maximum peak power density is 102 mW cm-2 for the Zn-air battery with an air cathode containing α-MnO2/XC-72 under an oxygen atmosphere when the carbon paper is 10AA. The specific capacity of all full-cell tests is higher than 750 mAh g-1 at all discharge current densities.

  9. Oxidation and Volatilization from Tantalum Alloy T-222 During Air Exposure

    SciTech Connect

    Smolik, G.R.; Petti, D.A.; Sharpe, J.P.; Schuetz, S.T.

    2000-10-31

    Tantalum alloys are one of the refractory metals with renewed consideration for high temperatures in fusion reactor applications. Tantalum alloys perform well in protective environments but oxidized readily in gases containing higher oxygen levels. In addition, the radioactive isotope Ta-182 would be produced in tantalum and could be a significant contributor to dose if mobilized. Other isotopes of importance are produced from tungsten and hafnium. Mobilization of activated products during an accident with air ingress is therefore a safety issue. In this study, we measured the extent of oxidation and mobilization from tantalum alloy T-222 oxidized in flowing air between 500 and 1200 C. This alloy nominally contains 10 wt% tungsten, 2.5 wt% hafnium and 0.01 wt% carbon. We found that the mobilization of Ta and Hf was closely linked to the occurrence of oxide spalling. These elements showed no migration from the test chamber. Some W was mobilized by volatilization as evidenced by transport from the chamber. Tungsten volatilization could occur primarily during initial stages of oxidation before an oxide scale forms and impedes the process. The mobilization of Ta and W are presented in terms of the mass flux (g/m 2 -h) as a function of test temperature. These measurements along with specific designs, activation calculations, and accident scenarios provide information useful for dose calculations of future fusion devices.

  10. Oxidation and Volatilization from Tantalum Alloy T-222 During Air Exposure

    SciTech Connect

    Smolik, Galen Richard; Petti, David Andrew; Sharpe, John Phillip; Schuetz, Stanley Thomas

    2000-10-01

    Tantalum alloys are one of the refractory metals with renewed consideration for high temperatures in fusion reactor applications. Tantalum alloys perform well in protective environments but oxidized readily in gases containing higher oxygen levels. In addition, the radioactive isotope Ta-182 would be produced in tantalum and could be a significant contributor to dose if mobilized. Other isotopes of importance are produced from tungsten and hafnium. Mobilization of activated products during an accident with air ingress is therefore a safety issue. In this study, we measured the extent of oxidation and mobilization from tantalum alloy T-222 oxidized in flowing air between 500 and 1200°C. This alloy nominally contains 10 wt% tungsten, 2.5 wt% hafnium and 0.01 wt% carbon. We found that the mobilization of Ta and Hf was closely linked to the occurrence of oxide spalling. These elements showed no migration from the test chamber. Some W was mobilized by volatilization as evidenced by transport from the chamber. Tungsten volatilization could occur primarily during initial stages of oxidation before an oxide scale forms and impedes the process. The mobilization of Ta and W are presented in terms of the mass flux (g/m 2 -h) as a function of test temperature. These measurements along with specific designs, activation calculations, and accident scenarios provide information useful for dose calculations of future fusion devices

  11. Soot Oxidation in Laminar Hydrocarbon/Air Diffusion Flames at Atmospheric Pressure. Appendix D

    NASA Technical Reports Server (NTRS)

    Xu, F.; El-Leathy, A. M.; Faeth, G. M.

    2000-01-01

    Soot oxidation was studied experimentally in laminar hydrocarbon/air diffusion flames at atmospheric pressure. Measurements were carried out along the axes of round jets burning in coflowing air considering acetylene, ethylene, proplyene and propane as fuels. Measurements were limited to the initial stages of soot oxidation (carbon consumption less than 70%) where soot oxidation mainly occurs at the surface of primary soot particles. The following properties were measured as a function of distance above the burner exit: soot concentrations by deconvoluted laser extinction, soot temperatures by deconvoluted multiline emission, soot structure by thermophoretic sampling and analysis using Transmission Electron Microscopy (TEM), concentrations of stable major gas species (N2, H2O, H2, 02, CO, CO2, CH4, C2H2, C2H4, C2H6, C3H6, and C3H8) by sampling and gas chromatography, concentrations of some radical species (H, OH, O) by the deconvoluted Li/LiOH atomic absorption technique and flow velocities by laser velocimetry. It was found that soot surface oxidation rates are not particularly affected by fuel type for laminar diffusion flames and are described reasonably well by the OH surface oxidation mechanism with a collision efficiency of 0.10, (standard deviation of 0.07) with no significant effect of fuel type in this behavior; these findings are in good agreement with the classical laminar premixed flame measurements of Neoh et al. Finally, direct rates of surface oxidation by O2 were small compared to OH oxidation for present conditions, based on estimated O2 oxidation rates due to Nagle and Strickland-Constable, because soot oxidation was completed near the flame sheet where O2 concentrations were less than 1.2% by volume.

  12. Soot Oxidation in Hydrocarbon/Air Diffusion Flames at Atmospheric Pressure. Appendix K

    NASA Technical Reports Server (NTRS)

    Xu, F.; El-Leathy, A. M.; Faeth, G. M.; Urban, D. L. (Technical Monitor); Yuan, Z.-G. (Technical Monitor)

    2001-01-01

    Soot oxidation was studied experimentally in laminar hydrocarbon/air diffusion flames at atmospheric pressure. Measurements were carried out along the axes of round jets burning in coflowing air considering acetylene, ethylene, propylene and propane as fuels. Measurements were limited to the initial stages of soot oxidation (carbon consumption less than 70%) where soot oxidation mainly occurs at the surface of primary soot particles. The following properties were measured as a function of distance above the burner exit: soot concentrations by deconvoluted laser extinction, soot temperatures by deconvoluted multiline emission, soot structure by thermophoretic sampling and analysis using Transmission Electron Microscopy (TEM), concentrations of stable major gas species (N2, H2O, H2, O2, CO, CO2, CH4, C2H2,C2H4, C2H6, C3H6, and C3H8) by sampling and gas chromatography, concentrations of some radical species (H, OH, O) by the deconvoluted Li/LiOH atomic absorption technique and flow velocities by laser velocimetry. It was found that soot surface oxidation rates are not particularly affected by fuel type for laminar diffusion flames and are described reasonably well by the OH surface oxidation mechanism with a collision efficiency of 0.10, (standard deviation of 0.07) with no significant effect of fuel type in this behavior; these findings are in good agreement with the classical laminar premixed flame measurements of Neoh et al. Finally, direct rates of surface oxidation by O2 were small compared to OH oxidation for present conditions, based on estimated O2 oxidation rates due to Nagle and Strickland-Constable (1962), because soot oxidation was completed near the flame sheet where O2 concentrations were less than 1.2% by volume.

  13. Oxidation kinetics of some nickel-based superalloy foils and electronic resistance of the oxide scale formed in air. Part 1

    SciTech Connect

    England, D.M.; Virkar, A.V.

    1999-09-01

    Haynes 230, Inconel 625, Inconel 718, and Hastelloy X foil specimens were oxidized in air for several thousand hours in the temperature range of 800--1,100 C. The oxidation kinetics of alloys studied obeyed the parabolic rate law. Haynes 230 exhibited the slowest oxidation kinetics of the alloys studied. X-ray diffraction, scanning electron microscopy, and electron probe microanalysis (EPMA) were the principal characterization tools employed. Chromium oxide, Cr{sub 2}O{sub 3}, was the predominant oxide phase in the oxide scale of all alloys studied. Manganese chromate was also detected in the oxide scales of Haynes 230, Hastelloy X, and Inconel 625. EPMA showed that the concentration of Mn in the oxide scale was much higher than in the alloy, indicating selective oxidation of Mn. The electronic resistance of the oxide scale was measured in air at temperatures up to 800 C on samples oxidized in air for up to several thousand hours. The oxide scale on Haynes 230 exhibited the lowest area-specific resistance, consistent with its slower oxidation kinetics.

  14. 40 CFR 50.11 - National primary and secondary ambient air quality standards for oxides of nitrogen (with...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 2 2010-07-01 2010-07-01 false National primary and secondary ambient... PRIMARY AND SECONDARY AMBIENT AIR QUALITY STANDARDS § 50.11 National primary and secondary ambient air... national primary annual ambient air quality standard for oxides of nitrogen is 53 parts per billion...

  15. 40 CFR Appendix S to Part 50 - Interpretation of the Primary National Ambient Air Quality Standards for Oxides of Nitrogen...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... Ambient Air Quality Standards for Oxides of Nitrogen (Nitrogen Dioxide) S Appendix S to Part 50 Protection... SECONDARY AMBIENT AIR QUALITY STANDARDS Pt. 50, App. S Appendix S to Part 50—Interpretation of the Primary... be submitted to EPA's Air Quality System (AQS), or otherwise available to EPA, meeting...

  16. Lichen communities on conifers in Southern California mountains: an ecological survey relative to oxidant air pollution

    SciTech Connect

    Sigal, L.L.; Nash, T.H. III

    1983-01-01

    In comparison with collections from the early 1900's when oxidant air pollution was essentially absent, 50% fewer lichen species were found on conifers during 3 yr (1976-1979) of collecting and sampling in the mountains of Southern California. Among the five mountain ranges studied, the San Bernardino Mountains, the region with the highest oxidant levels, had lower lichen frequency and cover values. Within the San Bernardino study sites, lichen cover was inversely related to estimated oxidant doses. Furthermore, at sites with high oxidant levels, marked morphological deterioration of the common species Hypogymnia enteromorpha was documented. Transplants of this species from the relatively unpolluted Cuyamaca Rancho State Park into the San Bernardino Mountains exhibited similar deterioration after a year's exposure. 4 figures, 9 tables.

  17. Lichen communities on conifers in Southern California mountains: an ecological survey relative to oxidant air pollution

    SciTech Connect

    Sigal, L.L.; Nash T.H. III

    1983-01-01

    In comparison with collections from the early 1900's when oxidant air pollution was essentially absent, 50% fewer lichen species were found on conifers during 3 yr (1976-1979) of collecting and sampling in the mountains of Southern California. Among the five mountain ranges studied, the San Bernardino Mountains, the region with the highest oxidant levels, had lower lichen frequency and cover values. Within the San Bernardino study sites, lichen cover was inversely related to estimated oxidant doses. Furthermore, at sites with high oxidant levels, marked morphological deterioration of the common species Hypogymnia enteromorpha was documented. Transplants of this species from the relatively unpolluted Cuyamaca Rancho State Park in the San Bernardino Mountains exhibited similar deterioration after a year's exposure.

  18. Air Oxidation Behavior of Two Ti-Base Alloys Synthesized by HIP

    NASA Astrophysics Data System (ADS)

    Liu, S.; Guo, Q. Q.; Liu, L. L.; Xu, L.; Liu, Y. Y.

    2016-04-01

    The oxidation behavior of Ti-5Al-2.5Sn and Ti-6Al-4V produced by hot isostatic pressing (HIP) has been studied at 650-850°C in air for 24 h. The oxidation kinetics of both alloys followed the parabolic law with good approximation, except for Ti-5Al-2.5Sn oxidized at 850°C. Multi-layered scales formed on both alloys at 750°C and 850°C. Ternary additions of Sn and V accounted for the different morphology of the scales formed on these two alloys. In addition, the oxidation behavior of HIP alloys is compared with that of the corresponding cast alloys and the scaling mechanism is discussed.

  19. Surface-catalyzed air oxidation reactions of hydrazines: Tubular reactor studies

    NASA Technical Reports Server (NTRS)

    Kilduff, Jan E.; Davis, Dennis D.; Koontz, Steven L.

    1988-01-01

    The surface-catalyzed air oxidation reactions of hydrazine, monomethylhydrazine, unsymmetrical dimethylhydrazine, symmetrical dimethylhydrazine, trimethylhydrazine and tetramethylhydrazine were investigated in a metal-powder packed turbular flow reactor at 55 plus or minus 3 C. Hydrazine was completely reacted on all surfaces studied. The major products of monomethylhydrazine (MMH) oxidation were methanol, methane and methyldiazene. The di-, tri- and tetra-methyl hydrazines were essentially unreactive under these conditions. The relative catalytic reactivities toward MMH are: Fe greater than Al2O3 greater than Ti greater than Zn greater than 316 SS greater than Cr greater than Ni greater than Al greater than 304L SS. A kinetic scheme and mechanism involving adsorption, oxidative dehydrogenation and reductive elimination reactions on a metal oxide surface are proposed.

  20. Effects of different surfaces on the transport and deposition of ruthenium oxides in high temperature air

    NASA Astrophysics Data System (ADS)

    Vér, N.; Matus, L.; Pintér, A.; Osán, J.; Hózer, Z.

    2012-01-01

    In order to understand the behaviour of ruthenium oxides in the reactor coolant system during an air ingress accident, new tests were performed in the frame of the RUSET (RUthenium Separate Effect Test) experimental program. These aimed to ascertain the effects of different surfaces (quartz, stainless steel (SS), zirconium alloy, alumina, oxidised metal, and surfaces with Mo or Cs deposits) on the transport and decomposition of ruthenium oxides in air stream along the temperature gradient zone (1100-100 °C). The results demonstrated that the heterogeneous phase decomposition of RuO 3 and RuO 4 to RuO 2 is catalysed more efficiently by the quartz surface than by the SS or alumina surfaces. The presence of MoO 3 layers decreased the RuO x precipitation extent on all investigated surfaces. The trapping effect of Cs deposit on Ru in the temperature gradient zone was proved in the case of the SS surface. On the contrary, presence of Cs precipitate on alumina and especially on quartz surfaces was found to decrease their catalytic effect on the decomposition of ruthenium oxides, and thus increased the RuO 4 concentration in the outlet air. Similarly to the effect observed for Cs deposition, the presence of other fission products in the evaporation area (at 1100 °C) decreased the partial pressure of RuO 4 in the outlet air at the SS surface and increased it at quartz and alumina surfaces. When zirconium (E110) cladding material was placed in the temperature gradient zone, no Ru transmittance occurred until the high temperature end of the zirconium tube was completely oxidised. After the intense oxidation of E110, Ru release occurred only in the presence of other fission product species. Pre-oxidation of SS surfaces in steam had no significant effect on the Ru passage.

  1. The Measurement of Fuel-Air Ratio by Analysis for the Oxidized Exhaust Gas

    NASA Technical Reports Server (NTRS)

    Gerrish, Harold C.; Meem, J. Lawrence, Jr.

    1943-01-01

    An investigation was made to determine a method of measuring fuel-air ratio that could be used for test purposes in flight and for checking conventional equipment in the laboratory. Two single-cylinder test engines equipped with typical commercial engine cylinders were used. The fuel-air ratio of the mixture delivered to the engines was determined by direct measurement of the quantity of air and of fuel supplied and also by analysis of the oxidized exhaust gas and of the normal exhaust gas. Five fuels were used: gasoline that complied with Army-Navy fuel Specification No. AN-VV-F-781 and four mixtures of this gasoline with toluene, benzene, and xylene. The method of determining the fuel-air ratio described in this report involves the measurement of the carbon-dioxide content of the oxidized exhaust gas and the use of graphs for the presented equation. This method is considered useful in aircraft, in the field, or in the laboratory for a range of fuel-air ratios from 0.047 to 0.124.

  2. The Measurement of Fuel-air Ratio by Analysis of the Oxidized Exhaust Gas

    NASA Technical Reports Server (NTRS)

    Memm, J. Lawrence, Jr.

    1943-01-01

    An investigation was made to determine a method of measuring fuel-air ratio that could be used for test purposes in flight and for checking conventional equipment in the laboratory. Two single-cylinder test engines equipped with typical commercial engine cylinders were used. The fuel-air ratio of the mixture delivered to the engines was determined by direct measurement of the quantity of air and of fuel supplied and also by analysis of the oxidized exhaust gas and of the normal exhaust gas. Five fuels were used: gasoline that complied with Army-Navy Fuel Specification, No. AN-VV-F-781 and four mixtures of this gasoline with toluene, benzene, and xylene. The method of determining the fuel-air ratio described in this report involves the measurement of the carbon-dioxide content of the oxidized exhaust gas and the use of graphs or the presented equation. This method is considered useful in aircraft, in the field, or in the laboratory for a range of fuel-air ratios from 0.047 to 0.124

  3. Oxidation of spent fuel in air at 175 degree to 195 degree C

    SciTech Connect

    Einziger, R.E.; Buchanan, H.C.; Thomas, L.E. ); Stout, R.B. )

    1992-04-01

    Oxidation tests in dry air were conducted on four LWR spent fuels at 175{degrees} and 195{degrees}C to determine the effect of the fuel characteristics on the oxidation state likely to exist at the time leaching occurs in a potential repository. Weight changes were measured and samples were examined by XRD, ceramography, TEM, and TGA. Despite local variations in the grain boundary susceptibility to oxidation, all four fuels progressed toward an apparent endpoint at an oxygen-to-metal (O/M) ratio of 2.4. The sole oxidation product was U{sub 4}O{sub 9+x,} a cubic phase structurally related to UO{sub 2} but with a slightly smaller lattice constant. The growth of the U{sub 4}O{sub 9+x} from the grain boundaries into the UO{sub 2} grains followed parabolic kinetics and had an activation energy of 26.6 kcal/mol. Based on the kinetics, the time required at 95{degrees}C to completely oxidize LWR spent fuel to U{sub 4}O{sub 9+x} would be at least 2000 yr. The next oxidation product to form after the U{sub 4}O{sub 9+x} phase may be U{sub 3}O{sub 8,} but no U{sub 3}O{sub 8} or other dilatational oxidation product has been detected in these accelerated tests conducted up to 25,000 h.

  4. Oxidation of spent fuel in air at 175{degree} to 195{degree}C

    SciTech Connect

    Einziger, R.E.; Buchanan, H.C.; Thomas, L.E.; Stout, R.B.

    1992-04-01

    Oxidation tests in dry air were conducted on four LWR spent fuels at 175{degrees} and 195{degrees}C to determine the effect of the fuel characteristics on the oxidation state likely to exist at the time leaching occurs in a potential repository. Weight changes were measured and samples were examined by XRD, ceramography, TEM, and TGA. Despite local variations in the grain boundary susceptibility to oxidation, all four fuels progressed toward an apparent endpoint at an oxygen-to-metal (O/M) ratio of 2.4. The sole oxidation product was U{sub 4}O{sub 9+x,} a cubic phase structurally related to UO{sub 2} but with a slightly smaller lattice constant. The growth of the U{sub 4}O{sub 9+x} from the grain boundaries into the UO{sub 2} grains followed parabolic kinetics and had an activation energy of 26.6 kcal/mol. Based on the kinetics, the time required at 95{degrees}C to completely oxidize LWR spent fuel to U{sub 4}O{sub 9+x} would be at least 2000 yr. The next oxidation product to form after the U{sub 4}O{sub 9+x} phase may be U{sub 3}O{sub 8,} but no U{sub 3}O{sub 8} or other dilatational oxidation product has been detected in these accelerated tests conducted up to 25,000 h.

  5. Oxidation Behavior and Mechanism of Pentlandite at 973 K (700 °C) in Air

    NASA Astrophysics Data System (ADS)

    Zhu, Huihui; Chen, Jun; Deng, Jinxia; Yu, Ranbo; Xing, Xianran

    2012-06-01

    The oxidation behavior of synthetic pentlandite at 973 K (700 °C) under isothermal conditions was investigated. The pentlandite sample (Ni,Fe)9S8 was synthesized from pure components and oxidized at 973 K (700 °C) in air in a muffle furnace. The phase identification and components analysis of the oxidation products were performed by using the Rietveld quantitative analysis method based on the powder X-ray diffraction (XRD) profiles and scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM-EDX). The magnetic hysteresis loops were determined by a vibrating sample magnetometer. Fe2O3, Ni x Fe3- x O4, and NiO were dominant oxidation products, and their weight fractions changed in different ways along with the oxidation time. The nickel-rich phase and sulfur-rich phase were observed as intermediate phases in unreacted cores during oxidation, which led to the formation of gaps and holes. The oxidation reaction rate was rapid in the first 2 hours, and then it slowed down sharply.

  6. In situ characterization of Zircaloy-4 oxidation at 500 °C in dry air

    NASA Astrophysics Data System (ADS)

    Vermoyal, J. J.; Dessemond, L.; Hammou, A.; Frichet, A.

    2001-10-01

    The in situ oxidation of Zircaloy-4 at 500 °C in dry air was investigated by thermogravimetric analysis (TGA) and electrochemical impedance spectroscopy (EIS). The coating of the alloy by a platinum film as electrode material was observed as not to modify the oxidation kinetic properties. After an initial cubic rate law, a transition to a quasi-linear curve occurs. The independence of the oxidation behavior to the Pt coupling is compatible with oxygen diffusion as the rate-determining step. During the pre-transition step, the rest potential of the cell Pt/oxide/Zy-4, the color of the oxide and the modulus of the single EIS signature indicate the high non-stoichiometry of the oxide. The kinetic transition was proposed to be correlated to the degradation of the film into a partially porous layer. This alteration of the oxide is associated to the appearance of a 1.2 V constant rest potential and the modification of the impedance diagrams in two high modulus contributions. The Cole-Cole representation has been used to demonstrate that the time variation of impedance spectra is related to the oxide growth. An equivalent circuit including two RC loops in series, whose capacitances are frequency dispersed, was proposed to be related to the film structure. Fitted data show that the thickness of the assumed protective layer of the film, close to the metal-oxide interface, is time independent in agreement with a constant oxidation rate. Finally, electrical properties of this inner layer were found to be quite different in pre- and post-transition stage.

  7. Laser Cladding to Improve Oxidation Behavior of Air Plasma-Sprayed Ni-20Cr Coating on Stainless Steel Substrate

    NASA Astrophysics Data System (ADS)

    Rauf, M. Mudassar; Shahid, Muhammad; Nusair Khan, A.; Mehmood, K.

    2015-09-01

    Air plasma-sprayed Ni-20Cr coating on stainless steel (AISI-304) substrate was re-melted using CO2 laser to remove the inherent defects, i.e., porosity, splat boundaries, and oxides of air plasma-sprayed coating. The (1) uncoated, (2) air plasma-sprayed, and (3) laser-re-melted specimens were exposed to cyclic oxidation at 900 °C for a hundred cycles run. The oxidation products were characterized using XRD and SEM. Weight changes were determined after every 4th cycle; Uncoated samples showed severe oxidation indicated by substantial weight loss, whereas air plasma-coated samples demonstrated noticeable weight gain. However, oxidation resistance of laser-cladded samples was found to be significantly improved as the samples showed negligible weight change; porosity within the coating was minimized with an improvement in interface quality causing reduction in delamination damage.

  8. Air oxidation behavior of fuel for the High Temperature Engineering Test Reactor (HTTR)

    NASA Astrophysics Data System (ADS)

    Kikuchi, Hironobu; Hayashi, Kimio; Fukuda, Kousaku

    1992-08-01

    The oxidation behavior of the HTTR fuel was studied with respect to the scenario of an air ingress accident which had been assessed in the HTTR safety analysis. The coated fuel particles were heated under a sufficient air flow in the temperature range of 900-1400 C for maximum duration of 600 h (at 1300 C). Failure fractions of the SiC coating layer after the heat treatments remained within the fraction at the fuel production. And the failure behavior of the SiC layer did not depend on such heating conditions as the temperature and the duration in the present experiment. It was confirmed by scanning electron microscopy (SEM), X-ray diffraction, and laser Raman spectroscopy that a thin oxide film was formed on the SiC layer by the heat treatments.

  9. Highly enantioselective oxidative couplings of 2-naphthols catalyzed by chiral bimetallic oxovanadium complexes with either oxygen or air as oxidant.

    PubMed

    Guo, Qi-Xiang; Wu, Zhi-Jun; Luo, Zhi-Bin; Liu, Quan-Zhong; Ye, Jian-Liang; Luo, Shi-Wei; Cun, Lin-Feng; Gong, Liu-Zhu

    2007-11-14

    The chiral bimetallic oxovanadium complexes have been designed for the enantioselective oxidative coupling of 2-naphthols bearing various substituents at C6 and/or C7. The chirality transferring from the amino acid to the axis of the biphenyl in oxovanadium complexes 2 was found to occur with the use of UV and CD spectra and DFT calculation. The homo-coupling reaction with oxygen as the oxidant was promoted by 5 mol % of an oxovanadium complex derived from L-isoleucine and achiral biphenol to afford binaphthols in nearly quantitative yields with high enantioselectivities of up to 98% ee. An oxovanadium complex derived from L-isoleucine and H8-binaphthol is highly efficient at catalyzing the air-oxidized coupling of 2-naphthols with excellent enantioselectivities of up to 97% ee. 51V NMR study shows that the oxovanadium complexes have two vanadium(V) species. Kinetic studies, the cross-coupling reaction, and HRMS spectral studies on the reaction have been carried out and illustrate that two vanadium(V) species are both involved in catalysis and that the coupling reaction undergoes a radical-radical mechanism in an intramolecular manner. Quantum mechanical calculations rationalize the importance of the cooperative effects of the axial chirality matching S-amino acids on the stereocontrol of the oxidative coupling reaction. The application of the transformation in the preparation of chiral ligands and conjugated polymers confirms the importance of the current process in organic synthesis. PMID:17956093

  10. 40 CFR Appendix T to Part 50 - Interpretation of the Primary National Ambient Air Quality Standards for Oxides of Sulfur (Sulfur...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Ambient Air Quality Standards for Oxides of Sulfur (Sulfur Dioxide) T Appendix T to Part 50 Protection of... Ambient Air Quality Standards for Oxides of Sulfur (Sulfur Dioxide) 1. General (a) This appendix explains... ambient air quality standards for Oxides of Sulfur as measured by Sulfur Dioxide (“SO2 NAAQS”)...

  11. 40 CFR Appendix T to Part 50 - Interpretation of the Primary National Ambient Air Quality Standards for Oxides of Sulfur (Sulfur...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... Ambient Air Quality Standards for Oxides of Sulfur (Sulfur Dioxide) T Appendix T to Part 50 Protection of... Ambient Air Quality Standards for Oxides of Sulfur (Sulfur Dioxide) 1. General (a) This appendix explains... ambient air quality standards for Oxides of Sulfur as measured by Sulfur Dioxide (“SO2 NAAQS”)...

  12. 40 CFR Appendix T to Part 50 - Interpretation of the Primary National Ambient Air Quality Standards for Oxides of Sulfur (Sulfur...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Ambient Air Quality Standards for Oxides of Sulfur (Sulfur Dioxide) T Appendix T to Part 50 Protection of... Ambient Air Quality Standards for Oxides of Sulfur (Sulfur Dioxide) 1. General (a) This appendix explains... ambient air quality standards for Oxides of Sulfur as measured by Sulfur Dioxide (“SO2 NAAQS”)...

  13. 40 CFR Appendix T to Part 50 - Interpretation of the Primary National Ambient Air Quality Standards for Oxides of Sulfur (Sulfur...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... Ambient Air Quality Standards for Oxides of Sulfur (Sulfur Dioxide) T Appendix T to Part 50 Protection of... Ambient Air Quality Standards for Oxides of Sulfur (Sulfur Dioxide) 1. General (a) This appendix explains... ambient air quality standards for Oxides of Sulfur as measured by Sulfur Dioxide (“SO2 NAAQS”)...

  14. Pyrrhotite Oxidation as an Indicator of Air Entrainment into Eruption Columns

    NASA Astrophysics Data System (ADS)

    Matsumoto, K.; Nakamura, M.

    2015-12-01

    Fragmented magmas in eruption columns obtain buoyancy by entrainment and heating of cold air. Theoretically, the proportion of the entrained air and temperature change of the magma fragments can be calculated through rigorous fluid dynamics, but these factors have not been evaluated from natural pyroclasts. In this study, we developed a new method for quantifying the degree of air entrainment based on pyrrhotite (Po) oxidation reactions, whose time scale corresponds to the typical duration of (sub-) Plinian eruptions (i.e., tens of seconds to a few hours). We examined pumice clasts and lava flows from the 1914-15 eruption of Sakurajima. During this event, various types of eruption were observed: Plinian eruptions with intermittent generation of clastogenic lava flow, followed by voluminous effusive lava flow. The products of Po oxidation consisted of magnetite (Mt), hematite (Hm), and their composites. The occurrence of Po and the oxides were systematically correlated with the types of eruption. In Plinian pumices, unreacted Po ± porous Mt-Hm composite reaction rims were dominant, whereas in the clastogenic lava, porous Hm occurred predominantly with scarce unreacted Po and porous Mt. In the effusive lava, a variety of Po, Mt, and Hm assemblage was observed, but Po did not coexist with Hm-rims. The porous Mt crystals in the pumice clasts were found to be Ti-free, whereas those in the effusive lava had Ti-enriched rims. These correlations were explained by considering two factors: the achieved fO2, which was controlled by the extent of fragmentation (i.e., surface area exposed to air), and duration of the maintenance of a high-T and high-fO2 condition. This study has demonstrated that the cooling timescale of pumice clasts in eruption columns can be estimated through the rate of Po oxidation reactions Po→Mt and Mt→Hm. Lavas of clastogenic origin may also be recognized from the reaction.

  15. Resistance Measurements and Activation Energies Calculations of Pure and Platinum Doped Stannic Oxide Ceramics in Air

    SciTech Connect

    Ibrahim, Zuhairi; Othman, Zulkafli; Karim, Mohd Mustamam Abd; Holland, Diane

    2007-05-09

    Pure SnO2 and Pt-SnO2 ceramics were fabricated by the dry pressing method using a pressure of 40 Mpa and sintered at 1000 deg. C. Electrical resistance measurements were made using an impedance analyzer, in air and temperatures between 25 deg. C and 450 deg. C. The change in resistance in both pure and platinum-doped stannic oxide ceramics was discussed.

  16. Air, aqueous and thermal stabilities of Ce3+ ions in cerium oxide nanoparticle layers with substrates.

    PubMed

    Naganuma, Tamaki; Traversa, Enrico

    2014-06-21

    Abundant oxygen vacancies coexisting with Ce(3+) ions in fluorite cerium oxide nanoparticles (CNPs) have the potential to enhance catalytic ability, but the ratio of unstable Ce(3+) ions in CNPs is typically low. Our recent work, however, demonstrated that the abundant Ce(3+) ions created in cerium oxide nanoparticle layers (CNPLs) by Ar ion irradiation were stable in air at room temperature. Ce valence states in CNPs correlate with the catalytic ability that involves redox reactions between Ce(3+) and Ce(4+) ions in given application environments (e.g. high temperature in carbon monoxide gas conversion and immersion conditions in biomedical applications). To better understand the mechanism by which Ce(3+) ions achieve stability in CNPLs, we examined (i) extra-long air-stability, (ii) thermal stability up to 500 °C, and (iii) aqueous stability of Ce(3+) ions in water, buffer solution and cell culture medium. It is noteworthy that air-stability of Ce(3+) ions in CNPLs persisted for more than 1 year. Thermal stability results showed that oxidation of Ce(3+) to Ce(4+) occurred at 350 °C in air. Highly concentrated Ce(3+) ions in ultra-thin CNPLs slowly oxidized in water within 1 day, but stability was improved in the cell culture medium. Ce(3+) stability of CNPLs immersed in the medium was associated with phosphorus adsorption on the Ce(3+) sites. This study also illuminates the potential interaction mechanisms of stable Ce(3+) ions in CNPLs. These findings could be utilized to understand catalytic mechanisms of CNPs with abundant oxygen vacancies in their application environments. PMID:24812662

  17. Amine-Oxide Hybrid Materials for CO2 Capture from Ambient Air.

    PubMed

    Didas, Stephanie A; Choi, Sunho; Chaikittisilp, Watcharop; Jones, Christopher W

    2015-10-20

    Oxide supports functionalized with amine moieties have been used for decades as catalysts and chromatographic media. Owing to the recognized impact of atmospheric CO2 on global climate change, the study of the use of amine-oxide hybrid materials as CO2 sorbents has exploded in the past decade. While the majority of the work has concerned separation of CO2 from dilute mixtures such as flue gas from coal-fired power plants, it has been recognized by us and others that such supported amine materials are also perhaps uniquely suited to extract CO2 from ultradilute gas mixtures, such as ambient air. As unique, low temperature chemisorbents, they can operate under ambient conditions, spontaneously extracting CO2 from ambient air, while being regenerated under mild conditions using heat or the combination of heat and vacuum. This Account describes the evolution of our activities on the design of amine-functionalized silica materials for catalysis to the design, characterization, and utilization of these materials in CO2 separations. New materials developed in our laboratory, such as hyperbranched aminosilica materials, and previously known amine-oxide hybrid compositions, have been extensively studied for CO2 extraction from simulated ambient air (400 ppm of CO2). The role of amine type and structure (molecular, polymeric), support type and structure, the stability of the various compositions under simulated operating conditions, and the nature of the adsorbed CO2 have been investigated in detail. The requirements for an effective, practical air capture process have been outlined and the ability of amine-oxide hybrid materials to meet these needs has been discussed. Ultimately, the practicality of such a "direct air capture" process is predicated not only on the physicochemical properties of the sorbent, but also how the sorbent operates in a practical process that offers a scalable gas-solid contacting strategy. In this regard, the utility of low pressure drop monolith

  18. A study of mercuric oxide and zinc-air battery life in hearing aids.

    PubMed

    Sparkes, C; Lacey, N K

    1997-09-01

    The requirement to phase out mercuric oxide (mercury) batteries on environmental grounds has led to the widespread introduction of zinc-air technology. The possibility arises that high drain hearing aids may not be adequately catered for by zinc-air cells, leading to poor performance. This study investigated the hearing aid user's ability to perceive differences between zinc-air and mercury cells in normal everyday usage. The data was collected for 100 experienced hearing aid users in field trials. Users report 50 per cent greater life for zinc-air cells in high power aids and 28 per cent in low power aids. The average life of the zinc-air cells range from 15 days in high power to 34 days in low power aids. Users are able to perceive a difference in sound quality in favour of zinc-air cells for low and medium power aids. The hearing aid population is not disadvantaged by phasing out mercury cells. PMID:9373545

  19. Using advanced oxidation treatment for biofilm inactivation by varying water vapor content in air plasma

    NASA Astrophysics Data System (ADS)

    Ryota, Suganuma; Koichi, Yasuoka

    2015-09-01

    Biofilms are caused by environmental degradation in food factories and medical facilities. The inactivation of biofilms involves making them react with chemicals including chlorine, hydrogen peroxide, and ozone, although inactivation using chemicals has a potential problem because of the hazardous properties of the residual substance and hydrogen peroxide, which have slow reaction velocity. We successfully performed an advanced oxidation process (AOP) using air plasma. Hydrogen peroxide and ozone, which were used for the formation of OH radicals in our experiment, were generated by varying the amount of water vapor supplied to the plasma. By varying the content of the water included in the air, the main product was changed from air plasma. When we increased the water content in the air, hydrogen peroxide was produced, while ozone peroxide was produced when we decreased the water content in the air. By varying the amount of water vapor, we realized a 99.9% reduction in the amount of bacteria in the biofilm when we discharged humidified air only. This work was supported by JSPS KAKENHI Grant Number 25630104.

  20. Formation and growth of indoor air aerosol particles as a result of D-limonene oxidation

    NASA Astrophysics Data System (ADS)

    Vartiainen, E.; Kulmala, M.; Ruuskanen, T. M.; Taipale, R.; Rinne, J.; Vehkamäki, H.

    Oxidation of D-limonene, which is a common monoterpene, can lead to new aerosol particle formation in indoor environments. Thus, products containing D-limonene, such as citrus fruits, air refresheners, household cleaning agents, and waxes, can act as indoor air aerosol particle sources. We released D-limonene into the room air by peeling oranges and measured the concentration of aerosol particles of three different size ranges. In addition, we measured the concentration of D-limonene, the oxidant, and the concentration of ozone, the oxidizing gas. Based on the measurements we calculated the growth rate of the small aerosol particles, which were 3-10 nm in diameter, to be about 6300nmh-1, and the losses of the aerosol particles that were due to the coagulation and condensation processes. From these, we further approximated the concentration of the condensable vapour and its source rate and then calculated the formation rate of the small aerosol particles. For the final result, we calculated the nucleation rate and the maximum number of molecules in a critical cluster. The nucleation rate was in the order of 105cm-3s-1 and the number of molecules in a critical-sized cluster became 1.2. The results were in agreement with the activation theory.

  1. Solid oxide fuel cells, and air electrode and electrical interconnection materials therefor

    DOEpatents

    Bates, J.L.

    1992-09-01

    In one aspect of the invention, an air electrode material for a solid oxide fuel cell comprises Y[sub 1[minus]a]Q[sub a]MnO[sub 3], where Q is selected from the group consisting of Ca and Sr or mixtures thereof and a' is from 0.1 to 0.8. Preferably, a' is from 0.4 to 0.7. In another aspect of the invention, an electrical interconnection material for a solid oxide fuel cell comprises Y[sub 1[minus]b]Ca[sub b]Cr[sub 1[minus]c]Al[sub c]O[sub 3], where b' is from 0.1 to 0.6 and c' is from 0 to 9.3. Preferably, b' is from 0.3 to 0.5 and c' is from 0.05 to 0.1. A composite solid oxide electrochemical fuel cell incorporating these materials comprises: a solid oxide air electrode and an adjacent solid oxide electrical interconnection which commonly include the cation Y, the air electrode comprising Y[sub 1[minus]a]Q[sub a]MnO[sub 3], where Q is selected from the group consisting of Ca and Sr or mixtures thereof and a' is from 0.1 to 0.8, the electrical interconnection comprising Y[sub 1[minus]b]Ca[sub b]Cr[sub 1[minus]c]Al[sub c]O[sub 3], where b' is from 0.1 to 0.6 and c' is from 0.0 to 0.3; a yttrium stabilized solid electrolyte comprising (1[minus]d)ZrO[sub 2]-(d)Y[sub 2]O[sub 3] where d' is from 0.06 to 0.5; and a solid fuel electrode comprising X-ZrO[sub 2], where X' is an elemental metal. 5 figs.

  2. Solid oxide fuel cells, and air electrode and electrical interconnection materials therefor

    DOEpatents

    Bates, J. Lambert

    1992-01-01

    In one aspect of the invention, an air electrode material for a solid oxide fuel cell comprises Y.sub.1-a Q.sub.a MnO.sub.3, where "Q" is selected from the group consisting of Ca and Sr or mixtures thereof and "a" is from 0.1 to 0.8. Preferably, "a" is from 0.4 to 0.7. In another aspect of the invention, an electrical interconnection material for a solid oxide fuel cell comprises Y.sub.1-b Ca.sub.b Cr.sub.1-c Al.sub.c O.sub.3, where "b" is from 0.1 to 0.6 and "c" is from 0 to 9.3. Preferably, "b" is from 0.3 to 0.5 and "c" is from 0.05 to 0.1. A composite solid oxide electrochemical fuel cell incorporating these materials comprises: a solid oxide air electrode and an adjacent solid oxide electrical interconnection which commonly include the cation Y, the air electrode comprising Y.sub.1-a Q.sub.a MnO.sub.3, where "Q" is selected from the group consisting of Ca and Sr or mixtures thereof and "a" is from 0.1 to 0.8, the electrical interconnection comprising Y.sub.1-b Ca.sub.b Cr.sub.1-c Al.sub.c O.sub.3, where "b" is from 0.1 to 0.6 and "c" is from 0.0 to 0.3; a yttrium stabilized solid electrolyte comprising (1-d)ZrO.sub.2 -(d)Y.sub.2 O.sub.3 where "d" is from 0.06 to 0.5; and a solid fuel electrode comprising X-ZrO.sub.2, where "X" is an elemental metal.

  3. Mortality from asthma and chronic bronchitis associated with changes in sulfur oxides air pollution

    SciTech Connect

    Imai, M.; Yoshida, K.; Kitabatake, M.

    1986-01-01

    Death certificates issued in Yokkaichi, Japan, during the 21 yr from 1963 until 1983 were surveyed to determine the relationship between changes in air pollution and mortality due to bronchial asthma and chronic bronchitis. The following results were obtained. In response to worsening air pollution, mortality for bronchial asthma and chronic bronchitis began to increase. Mortality due to bronchial asthma decreased immediately in response to improvement of pollution, whereas mortality due to chronic bronchitis decreased to the level in the control area 4 to 5 yr after the concentration of sulfur dioxide (SO/sub 2/) began to satisfy the ambient air quality standard. In the polluted area, mortality due to bronchial asthma in subjects who were 20 yr of age was higher during the period in which higher concentrations of sulfur oxides were prevalent.

  4. Evaluation of Ultra-Violet Photocatalytic Oxidation for Indoor AirApplications

    SciTech Connect

    Hodgson, A.T.; Sullivan, D.P.; Fisk, W.J.

    2006-02-01

    Acceptable indoor air quality in office buildings may be achieved with less energy by combining effective air cleaning systems for volatile organic compounds (VOCs) with particle filtration then by relying solely on ventilation. For such applications, ultraviolet photocatalytic oxidation (UVPCO) systems are being developed for VOC destruction. An experimental evaluation of a UVPCO system is reported. The evaluation was unique in that it employed complex mixtures of VOCs commonly found in office buildings at realistically low concentrations. VOC conversion efficiencies varied over a broad range, usually exceeded 20%, and were as high as {approx}80%. Conversion efficiency generally diminished with increased air flow rate. Significant amounts of formaldehyde and acetaldehyde were produced due to incomplete mineralization. The results indicate that formaldehyde and acetaldehyde production rates may need to be reduced before such UVPCO systems can be deployed safely in occupied buildings.

  5. Low cost stable air electrode material for high temperature solid oxide electrolyte electrochemical cells

    DOEpatents

    Kuo, L.J.H.; Singh, P.; Ruka, R.J.; Vasilow, T.R.; Bratton, R.J.

    1997-11-11

    A low cost, lanthanide-substituted, dimensionally and thermally stable, gas permeable, electrically conductive, porous ceramic air electrode composition of lanthanide-substituted doped lanthanum manganite is provided which is used as the cathode in high temperature, solid oxide electrolyte fuel cells and generators. The air electrode composition of this invention has a much lower fabrication cost as a result of using a lower cost lanthanide mixture, either a natural mixture or an unfinished lanthanide concentrate obtained from a natural mixture subjected to incomplete purification, as the raw material in place of part or all of the higher cost individual lanthanum. The mixed lanthanide primarily contains a mixture of at least La, Ce, Pr, and Nd, or at least La, Ce, Pr, Nd and Sm in its lanthanide content, but can also include minor amounts of other lanthanides and trace impurities. The use of lanthanides in place of some or all of the lanthanum also increases the dimensional stability of the air electrode. This low cost air electrode can be fabricated as a cathode for use in high temperature, solid oxide fuel cells and generators. 4 figs.

  6. Low cost stable air electrode material for high temperature solid oxide electrolyte electrochemical cells

    DOEpatents

    Kuo, Lewis J. H.; Singh, Prabhakar; Ruka, Roswell J.; Vasilow, Theodore R.; Bratton, Raymond J.

    1997-01-01

    A low cost, lanthanide-substituted, dimensionally and thermally stable, gas permeable, electrically conductive, porous ceramic air electrode composition of lanthanide-substituted doped lanthanum manganite is provided which is used as the cathode in high temperature, solid oxide electrolyte fuel cells and generators. The air electrode composition of this invention has a much lower fabrication cost as a result of using a lower cost lanthanide mixture, either a natural mixture or an unfinished lanthanide concentrate obtained from a natural mixture subjected to incomplete purification, as the raw material in place of part or all of the higher cost individual lanthanum. The mixed lanthanide primarily contains a mixture of at least La, Ce, Pr, and Nd, or at least La, Ce, Pr, Nd and Sm in its lanthanide content, but can also include minor amounts of other lanthanides and trace impurities. The use of lanthanides in place of some or all of the lanthanum also increases the dimensional stability of the air electrode. This low cost air electrode can be fabricated as a cathode for use in high temperature, solid oxide fuel cells and generators.

  7. Impact of clay mineral on air oxidation of PAH-contaminated soils.

    PubMed

    Biache, Coralie; Kouadio, Olivier; Lorgeoux, Catherine; Faure, Pierre

    2014-09-01

    This work investigated the impact of a clay mineral (bentonite) on the air oxidation of the solvent extractable organic matters (EOMs) and the PAHs from contaminated soils. EOMs were isolated from two coking plant soils and mixed with silica sand or bentonite. These samples, as well as raw soils and bentonite/soil mixtures, were oxidized in air at 60 and 100 °C for 160 days. Mineralization was followed by measuring the CO2 produced over the experiments. EOM, polycyclic aromatic compound (PAC), including PAH, contents were also determined. Oxidation led to a decrease in EOM contents and PAH concentrations, these diminutions were enhanced by the presence of bentonite. Transfer of carbon from EOM to insoluble organic matter pointed out a condensation phenomenon leading to a stabilization of the contamination. Higher mineralization rates, observed during the oxidation of the soil/bentonite mixtures, seem to indicate that this clay mineral had a positive influence on the transformation of PAC into CO2. PMID:24816462

  8. Removal of ammonia from air on molybdenum and tungsten oxide modified activated carbons.

    PubMed

    Petit, Camille; Bandosz, Teresa J

    2008-04-15

    Microporous coconut-based activated carbon was impregnated with solutions of ammonium metatungstate or ammonium molybdate and then calcined in air in order to convert the salts into their corresponding oxides. The surface of those materials was characterized using adsorption of nitrogen, potentiometric titration, Fourier-transform infrared spectroscopy, X-ray diffraction, and thermal analysis. The results indicated a significant increase in surface acidity related to the presence of tungsten or molybdenum oxides. On the materials obtained, adsorption of ammonia from either dry or moist air was carried out. The oxides distributed on the surface provided Lewis and/or Brønsted centers for interactions with ammonia molecules or ammonium ions. Water on the surface of carbon or in the gas phase increased the amount of ammonia adsorbed via involvement of Brønsted-type interactions and/or by leading to the formation of molybdate or tungstate salts on the surface. Although the amount of ammonia adsorbed is closely related to the number of moles of oxides and their acidic centers, the carbon surface also contributes to the adsorption via providing small pores where ammonia can be dissolved in the water film. PMID:18497162

  9. In situ secondary organic aerosol formation from ambient pine forest air using an oxidation flow reactor

    NASA Astrophysics Data System (ADS)

    Palm, B. B.; Campuzano-Jost, P.; Ortega, A. M.; Day, D. A.; Kaser, L.; Jud, W.; Karl, T.; Hansel, A.; Hunter, J. F.; Cross, E. S.; Kroll, J. H.; Peng, Z.; Brune, W. H.; Jimenez, J. L.

    2015-11-01

    Ambient air was oxidized by OH radicals in an oxidation flow reactor (OFR) located in a montane pine forest during the BEACHON-RoMBAS campaign to study biogenic secondary organic aerosol (SOA) formation and aging. High OH concentrations and short residence times allowed for semi-continuous cycling through a large range of OH exposures ranging from hours to weeks of equivalent (eq.) atmospheric aging. A simple model is derived and used to account for the relative time scales of condensation of low volatility organic compounds (LVOCs) onto particles, condensational loss to the walls, and further reaction to produce volatile, non-condensing fragmentation products. More SOA production was observed in the OFR at nighttime (average 4 μg m-3 when LVOC fate corrected) compared to daytime (average 1 μg m-3 when LVOC fate corrected), with maximum formation observed at 0.4-1.5 eq. days of photochemical aging. SOA formation followed a similar diurnal pattern to monoterpenes, sesquiterpenes, and toluene + p-cymene concentrations, including a substantial increase just after sunrise at 07:00 LT. Higher photochemical aging (> 10 eq. days) led to a decrease in new SOA formation and a loss of preexisting OA due to heterogeneous oxidation followed by fragmentation and volatilization. When comparing two different commonly used methods of OH production in OFRs (OFR185 and OFR254), similar amounts of SOA formation were observed. We recommend the OFR185 mode for future forest studies. Concurrent gas-phase measurements of air after OH oxidation illustrate the decay of primary VOCs, production of small oxidized organic compounds, and net production at lower ages followed by net consumption of terpenoid oxidation products as photochemical age increased. New particle formation was observed in the reactor after oxidation, especially during times when precursor gas concentrations and SOA formation were largest. Approximately 6 times more SOA was formed in the reactor from OH oxidation than

  10. Investigation of Room Temperature Oxidation of Cu in Air by Yoneda-XAFS

    SciTech Connect

    Keil, P.; Luetzenkirchen-Hecht, D.; Frahm, R.

    2007-02-02

    The structure of thin copper oxide layers which are formed on metallic Cu due to the exposure to air are investigated with Yoneda-XAFS and ReflEXAFS. The measured Yoneda-XAFS data were compared to quantitative model calculations in the framework of the distorted wave Born approximation (DWBA) assuming different model structures for the oxide layer. Yoneda-XAFS fine structure spectra measured for various different grazing angles show that the experimental data are best described by a model structure consisting of a duplex type oxide layer with an outer layer of CuO (tenorite) in direct contact with the gas atmosphere and an inner Cu2O (cuprite) layer at the interface to the underlying Cu metal.

  11. Carbon catalysis in the aqueous oxidation of SO2 by NO2 and air

    NASA Technical Reports Server (NTRS)

    Schryer, D. R.; Schryer, J.; Cofer, W. R., III; Vay, S. A.

    1984-01-01

    Sulfur dioxide and an oxidant gas (air or NO2) were bubbled through aqueous suspensions of both washed and unwashed carbon black as well as through samples of wash water, which contained whatever soluble species were originally present on the carbon, and high-purity water. The sulfate yields obtained showed the washed and unwashed carbon to be equally catalytic for the oxidation of SO2 to sulfate by both oxidants, whereas little sulfate was generated in either the wash water or high-purity water in the absence of carbon. These results indicate that the sulfate yields produced in aqueous suspensions of the carbon studied are due to catalysis by the carbon particles rather than by soluble species dissolved from them.

  12. Laboratory validation and field verification of a new passive air monitoring badge for sampling ethylene oxide in air.

    PubMed

    Kring, E V; Damrell, D J; Basilio, A N; McGibney, P D; Douglas, J J; Henry, T J; Ansul, G R

    1984-10-01

    A new diffusion colorimetric air monitoring badge for sampling ethylene oxide is described. The Du Pont Pro-Tek C-70 badge has been laboratory validated over the range of 4-375 ppm-hours (0.5-47 ppm on an 8-hour TWA) using standard spectrophotometer readout in 1 centimeter (10 mm) cells. The lower range can be extended to 2 ppm-hours (0.25 ppm) by using 4 cm (40 mm) cells. The badge has an overall sampling and analytical method accuracy of +/- 13.5%. It meets NIOSH accuracy criteria and has a mean coefficient of variation CVT = 0.059. The badge has no temperature, pressure, relative humidity or face velocity effects over practical ranges. The response time is adequate to sample peak concentrations over short time periods. The badge may be used to determine ambient formaldehyde levels if suspected to be present along with ethylene oxide. Badges are shown to agree very well with the industry accepted and proposed ASTM pump/charcoal tube method in three extensive plant field tests. Badges were more precise than the charcoal tube/pump method in all field tests conducted. PMID:6496316

  13. Cast Stone Oxidation Front Evaluation: Preliminary Results For Samples Exposed To Moist Air

    SciTech Connect

    Langton, C. A.; Almond, P. M.

    2013-11-26

    The rate of oxidation is important to the long-term performance of reducing salt waste forms because the solubility of some contaminants, e.g., technetium, is a function of oxidation state. TcO{sub 4}{sup -} in the salt solution is reduced to Tc(IV) and has been shown to react with ingredients in the waste form to precipitate low solubility sulfide and/or oxide phases. Upon exposure to oxygen, the compounds containing Tc(IV) oxidize to the pertechnetate ion, Tc(VII)O{sub 4}{sup -}, which is very soluble. Consequently the rate of technetium oxidation front advancement into a monolith and the technetium leaching profile as a function of depth from an exposed surface are important to waste form performance and ground water concentration predictions. An approach for measuring contaminant oxidation rate (effective contaminant specific oxidation rate) based on leaching of select contaminants of concern is described in this report. In addition, the relationship between reduction capacity and contaminant oxidation is addressed. Chromate (Cr(VI) was used as a non-radioactive surrogate for pertechnetate, Tc(VII), in Cast Stone samples prepared with 5 M Simulant. Cast Stone spiked with pertechnetate was also prepared and tested. Depth discrete subsamples spiked with Cr were cut from Cast Stone exposed to Savannah River Site (SRS) outdoor ambient temperature fluctuations and moist air. Depth discrete subsamples spiked with Tc-99 were cut from Cast Stone exposed to laboratory ambient temperature fluctuations and moist air. Similar conditions are expected to be encountered in the Cast Stone curing container. The leachability of Cr and Tc-99 and the reduction capacities, measured by the Angus-Glasser method, were determined for each subsample as a function of depth from the exposed surface. The results obtained to date were focused on continued method development and are preliminary and apply to the sample composition and curing / exposure conditions described in this report. The

  14. Flow mechanism for the long-range transport of air pollutants by the sea breeze causing inland nighttime high oxidants

    SciTech Connect

    Ueda, H.; Mitsumoto, S.; Kurita, H.

    1988-02-01

    Flow mechanism causing nightttime smog was investigated by analyzing 1) continuous records of meteorological data and concentration of oxidants (Ox) for 15 days and 2) aircraft data along the transportation route of a polluted air mass.

  15. DETECTION AND MOLECULAR ANALYSIS OF PARTICULATE AIR POLLUTION INDUCED CARDIOPULMONARY OXIDATIVE STRESS USING A TRANSGENIC MOUSE MODEL AND EMERGING TECHNOLOGIES

    EPA Science Inventory


    Identification of particle characteristics and biological mechanism(s) responsible for the adverse pulmonary and cardiovascular responses associated with particulate air pollution exposure remains a critical research activity. We have employed an oxidative stress sensitive an...

  16. Planar solid oxide fuel cell with staged indirect-internal air and fuel preheating and reformation

    DOEpatents

    Geisbrecht, Rodney A; Williams, Mark C

    2003-10-21

    A solid oxide fuel cell arrangement and method of use that provides internal preheating of both fuel and air in order to maintain the optimum operating temperature for the production of energy. The internal preheat passes are created by the addition of two plates, one on either side of the bipolar plate, such that these plates create additional passes through the fuel cell. This internal preheat fuel cell configuration and method reduce the requirements for external heat exchanger units and air compressors. Air or fuel may be added to the fuel cell as required to maintain the optimum operating temperature through a cathode control valve or an anode control valve, respectively. A control loop comprises a temperature sensing means within the preheat air and fuel passes, a means to compare the measured temperature to a set point temperature and a determination based on the comparison as to whether the control valves should allow additional air or fuel into the preheat or bypass manifolds of the fuel cell.

  17. Determination of hexavalent chromium in ambient air: A story of method induced Cr(III) oxidation

    NASA Astrophysics Data System (ADS)

    Tirez, Kristof; Silversmit, Geert; Bleux, Nico; Adriaensens, Elke; Roekens, Edward; Servaes, Kelly; Vanhoof, Chris; Vincze, Laszlo; Berghmans, Patrick

    2011-09-01

    The accuracy of the determination of Cr(VI) in ambient particulate matter remains a challenge from the point of view of minimal Cr species interconversion. Knowledge of this method induced oxidation and reduction is particularly relevant for the determination of Cr(VI) in ambient particulate matter, as the level of observed Cr(III) oxidation (average of 1.7% in this study) can contribute significantly to the monitored range of measured Cr(VI) in PM 10. For Cr concentrations in PM 10 > 10 ng Cr m -3, this method induced oxidation could lead to false positive exceeding of an air quality guideline value of 0.2 ng Cr(VI) m -3 in PM 10. The median daily Cr(VI) concentration in PM 10 measured over a monitoring period of more than 2 months at two locations close to a stainless steel factory amounted to 0.9 ng Cr(VI) m -3 and 0.27 ng Cr(VI) m -3. Average daily Cr(VI)/Cr ratios in PM 10 of 3.5% and 2.6% were measured at these locations. The described monitoring for the determination of Cr(VI) in ambient air via alkaline impregnated filters is sensitive (method detection limit of 0.015 ng Cr(VI) m -3) and reproducible (precision of the method ˜25%). The average Cr(VI) recovery of 75% strongly indicates the effects of ambient sampling conditions and ambient particles on the Cr(VI) recoveries. The stability of the Cr(VI) and the Cr(III) spike on 0.12 M NaHCO 3 impregnated filters observed with XANES, indicates that the alkaline extraction of the filter in combination with the sampled air matrix is likely to induce the Cr conversions. The XANES spectra shows further that a Cr-spinel is the predominant component of Cr in ambient air PM 10 at the monitored locations.

  18. OXIDATION OF INCONEL 718 IN AIR AT TEMPERATURES FROM 973K TO 1620K.

    SciTech Connect

    GREENE,G.A.; FINFROCK,C.C.

    2000-10-01

    As part of the APT project, it was necessary to quantify the release of tungsten from the APT spallation target during postulated accident conditions in order to develop accident source terms for accident consequence characterization. Experiments with tungsten rods at high temperatures in a flowing steam environment characteristic of postulated accidents revealed that considerable vaporization of the tungsten occurred as a result of reactions with the steam and that the aerosols which formed were readily transported away from the tungsten surfaces, thus exposing fresh tungsten to react with more steam. The resulting tungsten release fractions and source terms were undesirable and it was decided to clad the tungsten target with Inconel 718 in order to protect it from contact with steam during an accident and mitigate the accident source term and the consequences. As part of the material selection criteria, experiments were conducted with Inconel 718 at high temperatures to evaluate the rate of oxidation of the proposed clad material over as wide a temperature range as possible, as well as to determine the high-temperature failure limit of the material. Samples of Inconel 718 were inserted into a preheated furnace at temperatures ranging from 973 K to 1620 K and oxidized in air for varying periods of time. After oxidizing in air at a constant temperature for the prescribed time and then being allowed to cool, the samples would be reweighed to determine their weight gain due to the uptake of oxygen. From these weight gain measurements, it was possible to identify three regimes of oxidation for Inconel 718: a low-temperature regime in which the samples became passivated after the initial oxidation, an intermediate-temperature regime in which the rate of oxidation was limited by diffusion and exhibited a constant parabolic rate dependence, and a high-temperature regime in which material deformation and damage accompanied an accelerated oxidation rate above the parabolic

  19. Effect of inlet-air humidity on the formation of oxides of nitrogen in a gas-turbine combustor

    NASA Technical Reports Server (NTRS)

    Marchionna, N. R.

    1973-01-01

    Tests were conducted to determine the effect of inlet-air humidity on the formation of oxides of nitrogen from a gas-turbine combustor. Combustor inlet-air temperature ranged from 450 F to 1050 F. The tests were run at a constant pressure of 6 atmospheres and reference Mach number of 0.065. The NO sub x emission index was found to decrease with increasing inlet-air humidity at a constant exponential rate of 19 percent per mass percent water vapor in the air. This decrease of NO sub x emission index with increasing humidity was found to be independent of inlet-air temperature.

  20. Final report on international comparison CCQM-K68: Nitrous oxide in synthetic air

    NASA Astrophysics Data System (ADS)

    Lee, Jinbok; Lee, Jeongsoon; Moon, Dongmin; Seog Kim, Jin; Wessel, Rob; Aoki, Nobuyuki; Kato, Kenji; Guenther, Frank; Rhoderick, George; Konopelko, L. A.; Han, Qiao; Hall, Brad

    2011-01-01

    Nitrous oxide (N2O) is one of six greenhouse gases that are regulated by the Kyoto Protocol and has a Global Warming Potential (GWP) that is 296 times that of carbon dioxide. Global levels of nitrous oxide have increased at a rate of 0.25%/yr (0.8 ppb/yr) during the last ten years. In order to monitor levels of nitrous oxide in the atmosphere, it is necessary to use measurement standards with demonstrated equivalence at the highest level of accuracy. This report describes the results of a key comparison of standard gas mixtures of nitrous oxide in synthetic air at an amount fraction of 320 nmol/mol. This key comparison is part of the programme of the Gas Analysis Working Group (GAWG) of the CCQM to demonstrate the equivalence of the standards and measurement capabilities of the NMIs for greenhouse gases. It will support the development of measurement capability at the NMIs for nitrous oxide with uncertainties within the target set by the Global Atmospheric Watch (GAW) programme of the WMO for its global monitoring networks. Main text. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the CCQM, according to the provisions of the CIPM Mutual Recognition Arrangement (MRA).

  1. Exposure to Ultrafine Particles from Ambient Air and Oxidative Stress–Induced DNA Damage

    PubMed Central

    Bräuner, Elvira Vaclavik; Forchhammer, Lykke; Møller, Peter; Simonsen, Jacob; Glasius, Marianne; Wåhlin, Peter; Raaschou-Nielsen, Ole; Loft, Steffen

    2007-01-01

    Background Particulate matter, especially ultrafine particles (UFPs), may cause health effects through generation of oxidative stress, with resulting damage to DNA and other macromolecules. Objective We investigated oxidative damage to DNA and related repair capacity in peripheral blood mononuclear cells (PBMCs) during controlled exposure to urban air particles with assignment of number concentration (NC) to four size modes with average diameters of 12, 23, 57, and 212 nm. Design Twenty-nine healthy adults participated in a randomized, two-factor cross-over study with or without biking exercise for 180 min and with exposure to particles (NC 6169-15362/cm3) or filtered air (NC 91-542/cm3) for 24 hr. Methods The levels of DNA strand breaks (SBs), oxidized purines as formamidopyrimidine DNA glycolase (FPG) sites, and activity of 7,8-dihydro-8-oxoguanine-DNA glycosylase (OGG1) in PBMCs were measured by the Comet assay. mRNA levels of OGG1, nucleoside diphosphate linked moiety X-type motif 1 (NUDT1), and heme oxygenase-1 (HO1) were determined by real-time reverse transcriptase–polymerase chain reaction. Results Exposure to UFPs for 6 and 24 hr significantly increased the levels of SBs and FPG sites, with a further insignificant increase after physical exercise. The OGG1 activity and expression of OGG1, NUDT1, and HO1 were unaltered. There was a significant dose–response relationship between NC and DNA damage, with the 57-nm mode as the major contributor to effects. Concomitant exposure to ozone, nitrogen oxides, and carbon monoxide had no influence. Conclusion Our results indicate that UFPs, especially the 57-nm soot fraction from vehicle emissions, causes systemic oxidative stress with damage to DNA and no apparent compensatory up-regulation of DNA repair within 24 hr. PMID:17687444

  2. Impact of air pollution on oxidative DNA damage and lipid peroxidation in mothers and their newborns.

    PubMed

    Ambroz, Antonin; Vlkova, Veronika; Rossner, Pavel; Rossnerova, Andrea; Svecova, Vlasta; Milcova, Alena; Pulkrabova, Jana; Hajslova, Jana; Veleminsky, Milos; Solansky, Ivo; Sram, Radim J

    2016-08-01

    Ambient air particulate matter (PM) represents a class of heterogeneous substances that form one component of air pollution. Oxidative stress has been implicated as an important action mechanism for PM on the human organism. Oxidative damage induced by reactive oxygen species (ROS) may affect any cellular macromolecule. The aim of our study was to investigate the impact of air pollution on oxidative DNA damage [8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG)] and lipid peroxidation [15-F2t-isoprostane (15-F2t-IsoP)] in the urine and blood from mothers and newborns from two localities with different levels of air pollution: Ceske Budejovice (CB), a locality with a clean air, and Karvina, a locality with high air pollution. The samples from normal deliveries (38-41 week+) of nonsmoking mothers and their newborns were collected in the summer and winter seasons. Higher PM2.5 concentrations were found in Karvina than in CB in the summer 2013 (mean±SD: 20.41±6.28 vs. 9.45±3.62μg/m(3), P<0.001), and in the winter 2014 (mean±SD: 53.67±19.76 vs. 27.96±12.34μg/m(3), P<0.001). We observed significant differences in 15-F2t-IsoP levels between the summer and winter seasons in Karvina for newborns (mean±SD: 64.24±26.75 vs. 104.26±38.18pg/ml plasma, respectively) (P<0.001). Levels of 8-oxodG differed only in the winter season between localities, they were significantly higher (P<0.001) in newborns from Karvina in comparison with CB (mean±SD: 5.70±2.94 vs. 4.23±1.51 nmol/mmol creatinine, respectively). The results of multivariate regression analysis in newborns from Karvina showed PM2.5 concentrations to be a significant predictor for 8-oxodG excretion, PM2.5 and B[a]P (benzo[a]pyrene) concentrations to be a significant predictor for 15-F2t-IsoP levels. The results of multivariate regression analysis in mothers showed PM2.5 concentrations to be a significant predictor of 8-oxodG levels. PMID:27321041

  3. Airway inflammation and oxidative potential of air pollutant particles in a pediatric asthma panel

    PubMed Central

    Delfino, Ralph J.; Staimer, Norbert; Tjoa, Thomas; Gillen, Daniel L.; Schauer, James J.; Shafer, Martin M.

    2014-01-01

    Airborne particulate matter (PM) components from fossil fuel combustion can induce oxidative stress initiated by reactive oxygen species (ROS). Reported associations between worsening asthma and PM2.5 mass could be related to PM oxidative potential to induce airway oxidative stress and inflammation (hallmarks of asthma pathology). We followed 45 schoolchildren with persistent asthma in their southern California homes daily over 10 days with offline fractional exhaled nitric oxide (FENO), a biomarker of airway inflammation. Ambient exposures included daily average PM2.5, PM2.5 elemental and organic carbon (EC, OC), NO2, O3, and endotoxin. We assessed PM2.5 oxidative potential using both an abiotic and an in vitro bioassay on aqueous extracts of daily particle filters: (1) dithiothreitol (DTT) assay (abiotic), representing chemically produced ROS; and (2) ROS generated intracellularly in a rat alveolar macrophage model using the fluorescent probe 2′7′-dicholorohidroflourescin diacetate. We analyzed relations of FENO to air pollutants in mixed linear regression models. FENO was significantly positively associated with lag 1-day and 2-day averages of traffic-related markers (EC, OC, and NO2), DTT and macrophage ROS, but not PM2.5 mass. DTT associations were nearly twice as strong as other exposures per interquartile range: median FENO increased 8.7–9.9% per 0.43 nmole/min/m3 DTT. Findings suggest that future research in oxidative stress-related illnesses such as asthma and PM exposure would benefit from assessments of PM oxidative potential and composition. PMID:23673461

  4. Gas chromatograph analysis on closed air and nitrogen oxide storage atmospheres of recalcitrant seeds of Quercus Alba

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Storage of recalcitrant seeds remains an unsolved problem. This study investigated the quantitative gas analysis of nitrous oxide (N2O) and air atmospheres on the recalcitrant seeds of Quercus alba by using gas chromatograph. Ten seeds were placed in each sealed atmospheric system of air and 98/2% N...

  5. 77 FR 63827 - Request for Nominations of Experts for the Clean Air Scientific Advisory Committee (CASAC) Oxides...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-10-17

    ... of Nitrogen Primary National Ambient Air Quality Standards (NAAQS) Review Panel AGENCY: Environmental... the chartered CASAC on primary (human health-based) air quality standards for oxides of nitrogen (NO X... panel membership include: (a) Scientific and/or technical expertise, knowledge, and experience...

  6. Ruthenium-based electrocatalysts supported on reduced graphene oxide for lithium-air batteries.

    PubMed

    Jung, Hun-Gi; Jeong, Yo Sub; Park, Jin-Bum; Sun, Yang-Kook; Scrosati, Bruno; Lee, Yun Jung

    2013-04-23

    Ruthenium-based nanomaterials supported on reduced graphene oxide (rGO) have been investigated as air cathodes in non-aqueous electrolyte Li-air cells using a TEGDME-LiCF3SO3 electrolyte. Homogeneously distributed metallic ruthenium and hydrated ruthenium oxide (RuO2·0.64H2O), deposited exclusively on rGO, have been synthesized with average size below 2.5 nm. The synthesized hybrid materials of Ru-based nanoparticles supported on rGO efficiently functioned as electrocatalysts for Li2O2 oxidation reactions, maintaining cycling stability for 30 cycles without sign of TEGDME-LiCF3SO3 electrolyte decomposition. Specifically, RuO2·0.64H2O-rGO hybrids were superior to Ru-rGO hybrids in catalyzing the OER reaction, significantly reducing the average charge potential to ∼3.7 V at the high current density of 500 mA g(-1) and high specific capacity of 5000 mAh g(-1). PMID:23540570

  7. In situ secondary organic aerosol formation from ambient pine forest air using an oxidation flow reactor

    NASA Astrophysics Data System (ADS)

    Palm, Brett B.; Campuzano-Jost, Pedro; Ortega, Amber M.; Day, Douglas A.; Kaser, Lisa; Jud, Werner; Karl, Thomas; Hansel, Armin; Hunter, James F.; Cross, Eben S.; Kroll, Jesse H.; Peng, Zhe; Brune, William H.; Jimenez, Jose L.

    2016-03-01

    An oxidation flow reactor (OFR) is a vessel inside which the concentration of a chosen oxidant can be increased for the purpose of studying SOA formation and aging by that oxidant. During the BEACHON-RoMBAS (Bio-hydro-atmosphere interactions of Energy, Aerosols, Carbon, H2O, Organics & Nitrogen-Rocky Mountain Biogenic Aerosol Study) field campaign, ambient pine forest air was oxidized by OH radicals in an OFR to measure the amount of SOA that could be formed from the real mix of ambient SOA precursor gases, and how that amount changed with time as precursors changed. High OH concentrations and short residence times allowed for semicontinuous cycling through a large range of OH exposures ranging from hours to weeks of equivalent (eq.) atmospheric aging. A simple model is derived and used to account for the relative timescales of condensation of low-volatility organic compounds (LVOCs) onto particles; condensational loss to the walls; and further reaction to produce volatile, non-condensing fragmentation products. More SOA production was observed in the OFR at nighttime (average 3 µg m-3 when LVOC fate corrected) compared to daytime (average 0.9 µg m-3 when LVOC fate corrected), with maximum formation observed at 0.4-1.5 eq. days of photochemical aging. SOA formation followed a similar diurnal pattern to monoterpenes, sesquiterpenes, and toluene+p-cymene concentrations, including a substantial increase just after sunrise at 07:00 local time. Higher photochemical aging (> 10 eq. days) led to a decrease in new SOA formation and a loss of preexisting OA due to heterogeneous oxidation followed by fragmentation and volatilization. When comparing two different commonly used methods of OH production in OFRs (OFR185 and OFR254-70), similar amounts of SOA formation were observed. We recommend the OFR185 mode for future forest studies. Concurrent gas-phase measurements of air after OH oxidation illustrate the decay of primary VOCs, production of small oxidized organic

  8. In situ secondary organic aerosol formation from ambient pine forest air using an oxidation flow reactor

    DOE PAGESBeta

    Palm, Brett B.; Campuzano-Jost, Pedro; Ortega, Amber M.; Day, Douglas A.; Kaser, Lisa; Jud, Werner; Karl, Thomas; Hansel, Armin; Hunter, James F.; Cross, Eben S.; et al

    2016-03-08

    An oxidation flow reactor (OFR) is a vessel inside which the concentration of a chosen oxidant can be increased for the purpose of studying SOA formation and aging by that oxidant. During the BEACHON-RoMBAS (Bio-hydro-atmosphere interactions of Energy, Aerosols, Carbon, H2O, Organics & Nitrogen–Rocky Mountain Biogenic Aerosol Study) field campaign, ambient pine forest air was oxidized by OH radicals in an OFR to measure the amount of SOA that could be formed from the real mix of ambient SOA precursor gases, and how that amount changed with time as precursors changed. High OH concentrations and short residence times allowed formore » semicontinuous cycling through a large range of OH exposures ranging from hours to weeks of equivalent (eq.) atmospheric aging. A simple model is derived and used to account for the relative timescales of condensation of low-volatility organic compounds (LVOCs) onto particles; condensational loss to the walls; and further reaction to produce volatile, non-condensing fragmentation products. More SOA production was observed in the OFR at nighttime (average 3 µg m–3 when LVOC fate corrected) compared to daytime (average 0.9 µg m–3 when LVOC fate corrected), with maximum formation observed at 0.4–1.5 eq. days of photochemical aging. SOA formation followed a similar diurnal pattern to monoterpenes, sesquiterpenes, and toluene+p-cymene concentrations, including a substantial increase just after sunrise at 07:00 local time. Higher photochemical aging (>10 eq. days) led to a decrease in new SOA formation and a loss of preexisting OA due to heterogeneous oxidation followed by fragmentation and volatilization. When comparing two different commonly used methods of OH production in OFRs (OFR185 and OFR254-70), similar amounts of SOA formation were observed. We recommend the OFR185 mode for future forest studies. Concurrent gas-phase measurements of air after OH oxidation illustrate the decay of primary VOCs, production of small

  9. In situ secondary organic aerosol formation from ambient pine forest air using an oxidation flow reactor

    DOE PAGESBeta

    Palm, Brett B.; Campuzano-Jost, Pedro; Ortega, Amber M.; Day, Douglas A.; Kaser, Lisa; Jud, Werner; Karl, Thomas; Hansel, Armin; Hunter, James F.; Cross, Eben S.; et al

    2016-03-08

    An oxidation flow reactor (OFR) is a vessel inside which the concentration of a chosen oxidant can be increased for the purpose of studying SOA formation and aging by that oxidant. During the BEACHON-RoMBAS (Bio-hydro-atmosphere interactions of Energy, Aerosols, Carbon, H2O, Organics & Nitrogen–Rocky Mountain Biogenic Aerosol Study) field campaign, ambient pine forest air was oxidized by OH radicals in an OFR to measure the amount of SOA that could be formed from the real mix of ambient SOA precursor gases, and how that amount changed with time as precursors changed. High OH concentrations and short residence times allowed formore » semicontinuous cycling through a large range of OH exposures ranging from hours to weeks of equivalent (eq.) atmospheric aging. A simple model is derived and used to account for the relative timescales of condensation of low-volatility organic compounds (LVOCs) onto particles; condensational loss to the walls; and further reaction to produce volatile, non-condensing fragmentation products. More SOA production was observed in the OFR at nighttime (average 3 µg m−3 when LVOC fate corrected) compared to daytime (average 0.9 µg m−3 when LVOC fate corrected), with maximum formation observed at 0.4–1.5 eq. days of photochemical aging. SOA formation followed a similar diurnal pattern to monoterpenes, sesquiterpenes, and toluene+p-cymene concentrations, including a substantial increase just after sunrise at 07:00 local time. Higher photochemical aging (> 10 eq. days) led to a decrease in new SOA formation and a loss of preexisting OA due to heterogeneous oxidation followed by fragmentation and volatilization. When comparing two different commonly used methods of OH production in OFRs (OFR185 and OFR254-70), similar amounts of SOA formation were observed. We recommend the OFR185 mode for future forest studies. Concurrent gas-phase measurements of air after OH oxidation illustrate the decay of primary VOCs, production of

  10. In situ secondary organic aerosol formation from ambient pine forest air using an oxidation flow reactor

    SciTech Connect

    Palm, Brett B.; Campuzano-Jost, Pedro; Ortega, Amber M.; Day, Douglas A.; Kaser, Lisa; Jud, Werner; Karl, Thomas; Hansel, Armin; Hunter, James F.; Cross, Eben S.; Kroll, Jesse H.; Peng, Zhe; Brune, William H.; Jimenez, Jose L.

    2016-01-01

    An oxidation flow reactor (OFR) is a vessel inside which the concentration of a chosen oxidant can be increased for the purpose of studying SOA formation and aging by that oxidant. During the BEACHON-RoMBAS (Bio-hydro-atmosphere interactions of Energy, Aerosols, Carbon, H2O, Organics & Nitrogen–Rocky Mountain Biogenic Aerosol Study) field campaign, ambient pine forest air was oxidized by OH radicals in an OFR to measure the amount of SOA that could be formed from the real mix of ambient SOA precursor gases, and how that amount changed with time as precursors changed. High OH concentrations and short residence times allowed for semicontinuous cycling through a large range of OH exposures ranging from hours to weeks of equivalent (eq.) atmospheric aging. A simple model is derived and used to account for the relative timescales of condensation of low-volatility organic compounds (LVOCs) onto particles; condensational loss to the walls; and further reaction to produce volatile, non-condensing fragmentation products. More SOA production was observed in the OFR at nighttime (average 3 µg m−3 when LVOC fate corrected) compared to daytime (average 0.9 µg m−3 when LVOC fate corrected), with maximum formation observed at 0.4–1.5 eq. days of photochemical aging. SOA formation followed a similar diurnal pattern to monoterpenes, sesquiterpenes, and toluene+p-cymene concentrations, including a substantial increase just after sunrise at 07:00 local time. Higher photochemical aging (> 10 eq. days) led to a decrease in new SOA formation and a loss of preexisting OA due to heterogeneous oxidation followed by fragmentation and volatilization. When comparing two different commonly used methods of OH production in OFRs (OFR185 and OFR254-70), similar amounts of SOA formation were observed. We recommend the OFR185 mode for future forest studies. Concurrent gas-phase measurements of air after OH oxidation illustrate the

  11. Alternative materials for solid oxide fuel cells: Factors affecting air-sintering of chromite interconnections

    SciTech Connect

    Chick, L.A.; Bates, J.L.

    1992-07-01

    The purpose of this research is to develop alternative materials for solid oxide fuel cell (SOFC) interconnections and electrodes with improved electrical, thermal and electrochemical properties. Another objective is to develop synthesis and fabrication processes for these materials whereby they can be consolidated in air into SOFCs. The approach is to (1) develop modifications of the current, state-of-the-art materials used in SOFCs, (2) minimize the number of cations used in the SOFC materials to reduce potential deleterious interactions, (3) improve thermal, electrical, and electrochemical properties, (4) develop methods to synthesize both state-of-the-art and alternative materials for the simultaneous fabrication and consolidation in air of the interconnections and electrodes with the solid electrolyte, and (5) understand electrochemical reactions at materials interfaces and the effects of component compositions and processing on those reactions.

  12. Retrieval of the Nitrous Oxide Profiles using the AIRS Data in China

    NASA Astrophysics Data System (ADS)

    Chen, L.; Ma, P.; Tao, J.; Li, X.; Zhang, Y.; Wang, Z.; Li, S.; Xiong, X.

    2014-12-01

    As an important greenhouse gas and ozone-depleting substance, the 100-year global warming potential of Nitrous Oxide (N2O) is almost 300 times higher than that of carbon dioxide. However, there are still large uncertainties about the quantitative N2O emission and its feedback to climate change due to the coarse ground-based network. This approach attempts to retrieve the N2O profiles from the Atmospheric InfraRed Sounder (AIRS) data. First, the sensitivity of atmospheric temperature and humidity profiles and surface parameters between two spectral absorption bands were simulated by using the radiative transfer model. Second, the eigenvector regression algorithm is used to construct a priori state. Third, an optimal estimate method was developed based on the band selection of N2O. Finally, we compared our retrieved AIRS profiles with HIPPO data, and analyzed the seasonal and annual N2O distribution in China from 2004 to 2013.

  13. Thin porous indium tin oxide nanoparticle films: effects of annealing in vacuum and air

    NASA Astrophysics Data System (ADS)

    Ederth, J.; Hultåker, A.; Niklasson, G. A.; Heszler, P.; van Doorn, A. R.; Jongerius, M. J.; Burgard, D.; Granqvist, C. G.

    2005-11-01

    Electrical and optical properties were investigated in porous thin films consisting of In2O3:Sn (indium tin oxide; ITO) nanoparticles. The temperature-dependent resistivity was successfully described by a fluctuation-induced tunneling model, indicating a sample morphology dominated by clusters of ITO nanoparticles separated by insulating barriers. An effective-medium model, including the effect of ionized impurity scattering, was successfully fitted to measured reflectance and transmittance. Post-deposition treatments were carried out at 773 K for 2 h in both air and vacuum. It is shown that vacuum annealing increases either the barrier width or the area between two conducting clusters in the samples and, furthermore, an extra optical absorption occurs close to the band gap. A subsequent air annealing then reduces the effect of the barriers on the electrical properties and diminishes the absorption close to the band gap.

  14. Microleakage on Class V glass ionomer restorations after cavity preparation with aluminum oxide air abrasion.

    PubMed

    Corona, Silmara Aparecida Milori; Borsatto, Maria Cristina; Rocha, Renata Andréa Salvitti de Sá; Palma-Dibb, Regina Guenka

    2005-01-01

    This in vitro study assessed the marginal microleakage on class V cavities prepared with aluminum oxide air abrasion and restored with different glass ionomer cements. The cavities were prepared on the buccal and lingual surfaces of 15 sound third molars with an air- abrasion device (Kreativ Mach 4.1; New Image) using a 27.5-microm aluminum oxide particle stream, and were assigned to 3 groups of 10 cavities each. The restorative materials were: group I, a conventional glass ionomer cement (Ketac-Fil); groups II and III, resin-modified glass ionomer cements (Vitremer R and Fuji II LC, respectively). After placement of the restorations, the teeth were stored in distilled water at 37 degrees C for 24 h, polished and then submitted to a thermocycling regimen of 500 cycles, isolated, immersed in 0.2% Rhodamine B solution for 24 h, included and serially sectioned. Microleakage was assessed by viewing the specimens under an optical microscope connected to a color video camera and a computer. The images obtained were digitized and analyzed for microleakage using software that allows for a standard quantitative assessment of dye penetration in millimeters. Statistical analysis was done using the Kruskall-Wallis and Wilcoxon tests. Means of dye penetration (%) were: occlusal - I: 25.76 +/- 34.35, II: 20.00 +/- 42.16, III: 28.25 +/- 41.67; cervical - I: 23.72 +/- 41.84; II: 44.22 +/- 49.69, III: 39.27 +/- 50.74. No statistically significant differences (p>0.05) were observed among either the glass ionomer cements or the margins. In conclusion, class V cavities restored with either conventional or resin-modified glass ionomer cements after preparation with aluminum oxide air abrasion did not show complete sealing at the enamel and dentin/cementum margins. PMID:16113931

  15. Lanthanum manganite-based air electrode for solid oxide fuel cells

    DOEpatents

    Ruka, Roswell J.; Kuo, Lewis; Li, Baozhen

    1999-01-01

    An air electrode material for a solid oxide fuel cell is disclosed. The electrode material is based on lanthanum manganite having a perovskite-like crystal structure ABO.sub.3. The A-site of the air electrode material preferably comprises La, Ca, Ce and at least one lanthanide selected from Sm, Gd, Dy, Er, Y and Nd. The B-site of the electrode material comprises Mn with substantially no dopants. The ratio of A:B is preferably slightly above 1. A preferred air electrode composition is of the formula La.sub.w Ca.sub.x Ln.sub.y Ce.sub.z MnO.sub.3, wherein Ln comprises at least one lanthanide selected from Sm, Gd, Dy, Er, Y and Nd, w is from about 0.55 to about 0.56, x is from about 0.255 to about 0.265, y is from about 0.175 to about 0.185, and z is from about 0.005 to about 0.02. The air electrode material possesses advantageous chemical and electrical properties as well as favorable thermal expansion and thermal cycle shrinkage characteristics.

  16. Lanthanum manganite-based air electrode for solid oxide fuel cells

    DOEpatents

    Ruka, R.J.; Kuo, L.; Li, B.

    1999-06-29

    An air electrode material for a solid oxide fuel cell is disclosed. The electrode material is based on lanthanum manganite having a perovskite-like crystal structure ABO[sub 3]. The A-site of the air electrode material preferably comprises La, Ca, Ce and at least one lanthanide selected from Sm, Gd, Dy, Er, Y and Nd. The B-site of the electrode material comprises Mn with substantially no dopants. The ratio of A:B is preferably slightly above 1. A preferred air electrode composition is of the formula La[sub w]Ca[sub x]Ln[sub y]Ce[sub z]MnO[sub 3], wherein Ln comprises at least one lanthanide selected from Sm, Gd, Dy, Er, Y and Nd, w is from about 0.55 to about 0.56, x is from about 0.255 to about 0.265, y is from about 0.175 to about 0.185, and z is from about 0.005 to about 0.02. The air electrode material possesses advantageous chemical and electrical properties as well as favorable thermal expansion and thermal cycle shrinkage characteristics. 10 figs.

  17. Incipient oxidation kinetics of alloy 617 and residual stress of the oxide scale formed in air at temperatures between 850 and 1000 °C

    NASA Astrophysics Data System (ADS)

    Tung, Hsiao-Ming; Stubbins, James F.

    2012-05-01

    The purpose of this study was to investigate incipient oxidation of alloy 617 in air in the temperature range of 850-1000 °C. Alloy 617 exhibited a two-stage oxidation kinetics and followed Wagner's parabolic law. The activation energy for the first stage and the second stage are 271.2 and 318 kJ/mol, respectively. The transition time between the two stages decreased as the oxidation temperature increased. X-ray diffraction (XRD) revealed that the oxide phase is chromium oxide, Cr2O3, over the entire temperature range. The results of residual stress measurements showed that the grown-in stresses of the scale are tensile in nature. This may be due to the crystallite coalescence during the growth of the oxide. The measured residual stress of the substrate decreases with increasing oxidation temperature which may be attributed to the formation of pores or voids within the substrate after exposure to high temperatures.

  18. SPONTANEOUS CATALYTIC WET AIR OXIDATION DURING PRE-TREATMENT OF HIGH-LEVEL RADIOACTIVE WASTE SLUDGE

    SciTech Connect

    Koopman, D.; Herman, C.; Pareizs, J.; Bannochie, C.; Best, D.; Bibler, N.; Fellinger, T.

    2009-10-01

    Savannah River Remediation, LLC (SRR) operates the Defense Waste Processing Facility for the U.S. Department of Energy at the Savannah River Site. This facility immobilizes high-level radioactive waste through vitrification following chemical pretreatment. Catalytic destruction of formate and oxalate ions to carbon dioxide has been observed during qualification testing of non-radioactive analog systems. Carbon dioxide production greatly exceeded hydrogen production, indicating the occurrence of a process other than the catalytic decomposition of formic acid. Statistical modeling was used to relate the new reaction chemistry to partial catalytic wet air oxidation of both formate and oxalate ions driven by the low concentrations of palladium, rhodium, and/or ruthenium in the waste. Variations in process conditions led to increases or decreases in the total oxidative destruction, as well as partially shifting the preferred species undergoing destruction from oxalate ion to formate ion.

  19. Carbon-catalyzed oxidation of SO2 by NO2 and air

    NASA Technical Reports Server (NTRS)

    Rogowski, R. S.; Schryer, D. R.; Cofer, W. R., III; Edahl, R. A., Jr.; Munavalli, S.

    1982-01-01

    A series of experiments was performed using carbon particles (commercial furnace black) as a surrogate for soot particles. Carbon particles were suspended in water, and gas mixtures were bubbled into the suspensions to observe the effect of carbon particles on the oxidation of SO2 by air and NO2. Identical gas mixtures were bubbled into a blank containing only pure water. After exposure each solution was analyzed for pH and sulfate. It was found that NO2 greatly enhances the oxidation of SO2 to sulfate in the presence of carbon particles. The amount of sulfate found in the blanks was significantly less. Under the conditions of these experiments no saturation of the reaction was observed and SO2 was converted to sulfate even in a highly acid medium (pH or = 1.5).

  20. Oxidation of SO2 by NO2 and air in an aqueous suspension of carbon

    NASA Technical Reports Server (NTRS)

    Rogowski, R. S.; Schryer, D. R.; Cofer, W. R., III; Edahl, R. A., Jr.; Munavalli, S.

    1982-01-01

    A series of experiments has been performed using carbon black as a surrogate for soot particles. Carbon black was suspended in water and gas mixtures were bubbled into the suspensions to observe the effect of carbon particles on the oxidation of SO2 by air and NO2. Identical gas mixtures were bubbled into a black containing only pure water. After exposure each solution was analyzed for pH and sulfate. It was found that NO2 greatly enhances the oxidation of SO2 to sulfate in the presence of carbon black. The amount of sulfate in the blanks was significantly less. Under the conditions of the experiments no saturation of the reaction was observed and SO2 was converted to sulfate even in a highly acid medium (pH not less than 1.5).

  1. Oxidative Nitration of Styrenes for the Recycling of Low-Concentrated Nitrogen Dioxide in Air.

    PubMed

    Hofmann, Dagmar; de Salas, Cristina; Heinrich, Markus R

    2015-09-21

    The oxidative nitration of styrenes in ethyl acetate represents a metal-free, environmentally friendly, and sustainable technique to recover even low concentrations of NO2 in air. Favorable features are that the product mixture comprising nitroalcohols, nitroketones, and nitro nitrates simplifies at lower concentrations of NO2 . Experiments in a miniplant-type 10 L wet scrubber demonstrated that the recycling technique is well applicable on larger scales at which initial NO2 concentrations of >10 000 ppm were reliably reduced to less than 40 ppm. PMID:26284827

  2. Budgets for nocturnal VOC oxidation by nitrate radicals aloft during the 2006 Texas Air Quality Study

    NASA Astrophysics Data System (ADS)

    Brown, Steven S.; Dubé, William P.; Peischl, Jeff; Ryerson, Thomas B.; Atlas, Elliot; Warneke, Carsten; de Gouw, Joost A.; Te Lintel Hekkert, Sacco; Brock, Charles A.; Flocke, Frank; Trainer, Michael; Parrish, David D.; Feshenfeld, Frederick C.; Ravishankara, A. R.

    2011-12-01

    Industrial emissions in Houston, Texas, and along the U.S. Gulf Coast are a large source of highly reactive anthropogenic volatile organic compounds (VOCs), principally alkenes, that affect air quality in that region. Nighttime oxidation by either O3 or NO3 removes these VOCs. This paper presents a regional analysis of nighttime P-3 flights during the 2006 Texas Air Quality Study (TexAQS) to quantify the loss rates and budgets for both NO3 and highly reactive VOC. Mixing ratios and production rates of NO3 were large, up to 400 parts per trillion by volume (pptv) and 1-2 parts per billion by volume (ppbv) per hour, respectively. Budgets for NO3 show that it was lost primarily to reaction with VOCs, with the sum of anthropogenic VOCs (30-54%) and isoprene (10-50%) being the largest contributors. Indirect loss of NO3 to N2O5 hydrolysis was of lesser importance (14-28%) but was the least certain due to uncertainty in the aerosol uptake coefficient for N2O5. Reaction of NO3 with peroxy radicals was a small but nonzero contribution to NO3 loss but was also uncertain because there were no direct measurements of peroxy radicals. Net VOC oxidation rates were rapid (up to 2 ppbv VOC h-1 in industrial plumes) and were dominated by NO3, which was 3-5 times more important as an oxidant than O3. Plumes of high NO3 reactivity (i.e., short steady state lifetimes, on the order of 1 min) identified the presence of concentrated emissions of highly reactive VOCs from the Houston Ship Channel (HSC), which, depending on the particular VOC, may be efficiently oxidized during overnight transport.

  3. Air oxidation of Zircaloy-4 in the 600-1000 °C temperature range: Modeling for ASTEC code application

    NASA Astrophysics Data System (ADS)

    Coindreau, O.; Duriez, C.; Ederli, S.

    2010-10-01

    Progress in the treatment of air oxidation of zirconium in severe accident (SA) codes are required for a reliable analysis of severe accidents involving air ingress. Air oxidation of zirconium can actually lead to accelerated core degradation and increased fission product release, especially for the highly-radiotoxic ruthenium. This paper presents a model to simulate air oxidation kinetics of Zircaloy-4 in the 600-1000 °C temperature range. It is based on available experimental data, including separate-effect experiments performed at IRSN and at Forschungszentrum Karlsruhe. The kinetic transition, named "breakaway", from a diffusion-controlled regime to an accelerated oxidation is taken into account in the modeling via a critical mass gain parameter. The progressive propagation of the locally initiated breakaway is modeled by a linear increase in oxidation rate with time. Finally, when breakaway propagation is completed, the oxidation rate stabilizes and the kinetics is modeled by a linear law. This new modeling is integrated in the severe accident code ASTEC, jointly developed by IRSN and GRS. Model predictions and experimental data from thermogravimetric results show good agreement for different air flow rates and for slow temperature transient conditions.

  4. Raman spectroscopy analysis of air grown oxide scale developed on pure zirconium substrate

    NASA Astrophysics Data System (ADS)

    Kurpaska, L.; Favergeon, J.; Lahoche, L.; El-Marssi, M.; Grosseau Poussard, J.-L.; Moulin, G.; Roelandt, J.-M.

    2015-11-01

    Using Raman spectroscopy technique, external and internal parts of zirconia oxide films developed at 500 °C and 600 °C on pure zirconium substrate under air at normal atmospheric pressure have been examined. Comparison of Raman peak positions of tetragonal and monoclinic zirconia phases, recorded during the oxide growth at elevated temperature, and after cooling at room temperature have been presented. Subsequently, Raman peak positions (or shifts) were interpreted in relation with the stress evolution in the growing zirconia scale, especially closed to the metal/oxide interface, where the influence of compressive stress in the oxide is the biggest. Reported results, for the first time show the presence of a continuous layer of tetragonal zirconia phase developed in the proximity of pure zirconium substrate. Based on the Raman peak positions we prove that this tetragonal layer is stabilized by the high compressive stress and sub-stoichiometry level. Presence of the tetragonal phase located in the outer part of the scale have been confirmed, yet its Raman characteristics suggest a stress-free tetragonal phase, therefore different type of stabilization mechanism. Presented study suggest that its stabilization could be related to the lattice defects introduced by highstoichiometry of zirconia or presence of heterovalent cations.

  5. One-dimensional manganese-cobalt oxide nanofibres as bi-functional cathode catalysts for rechargeable metal-air batteries

    PubMed Central

    Jung, Kyu-Nam; Hwang, Soo Min; Park, Min-Sik; Kim, Ki Jae; Kim, Jae-Geun; Dou, Shi Xue; Kim, Jung Ho; Lee, Jong-Won

    2015-01-01

    Rechargeable metal-air batteries are considered a promising energy storage solution owing to their high theoretical energy density. The major obstacles to realising this technology include the slow kinetics of oxygen reduction and evolution on the cathode (air electrode) upon battery discharging and charging, respectively. Here, we report non-precious metal oxide catalysts based on spinel-type manganese-cobalt oxide nanofibres fabricated by an electrospinning technique. The spinel oxide nanofibres exhibit high catalytic activity towards both oxygen reduction and evolution in an alkaline electrolyte. When incorporated as cathode catalysts in Zn-air batteries, the fibrous spinel oxides considerably reduce the discharge-charge voltage gaps (improve the round-trip efficiency) in comparison to the catalyst-free cathode. Moreover, the nanofibre catalysts remain stable over the course of repeated discharge-charge cycling; however, carbon corrosion in the catalyst/carbon composite cathode degrades the cycling performance of the batteries. PMID:25563733

  6. One-dimensional manganese-cobalt oxide nanofibres as bi-functional cathode catalysts for rechargeable metal-air batteries.

    PubMed

    Jung, Kyu-Nam; Hwang, Soo Min; Park, Min-Sik; Kim, Ki Jae; Kim, Jae-Geun; Dou, Shi Xue; Kim, Jung Ho; Lee, Jong-Won

    2015-01-01

    Rechargeable metal-air batteries are considered a promising energy storage solution owing to their high theoretical energy density. The major obstacles to realising this technology include the slow kinetics of oxygen reduction and evolution on the cathode (air electrode) upon battery discharging and charging, respectively. Here, we report non-precious metal oxide catalysts based on spinel-type manganese-cobalt oxide nanofibres fabricated by an electrospinning technique. The spinel oxide nanofibres exhibit high catalytic activity towards both oxygen reduction and evolution in an alkaline electrolyte. When incorporated as cathode catalysts in Zn-air batteries, the fibrous spinel oxides considerably reduce the discharge-charge voltage gaps (improve the round-trip efficiency) in comparison to the catalyst-free cathode. Moreover, the nanofibre catalysts remain stable over the course of repeated discharge-charge cycling; however, carbon corrosion in the catalyst/carbon composite cathode degrades the cycling performance of the batteries. PMID:25563733

  7. One-dimensional manganese-cobalt oxide nanofibres as bi-functional cathode catalysts for rechargeable metal-air batteries

    NASA Astrophysics Data System (ADS)

    Jung, Kyu-Nam; Hwang, Soo Min; Park, Min-Sik; Kim, Ki Jae; Kim, Jae-Geun; Dou, Shi Xue; Kim, Jung Ho; Lee, Jong-Won

    2015-01-01

    Rechargeable metal-air batteries are considered a promising energy storage solution owing to their high theoretical energy density. The major obstacles to realising this technology include the slow kinetics of oxygen reduction and evolution on the cathode (air electrode) upon battery discharging and charging, respectively. Here, we report non-precious metal oxide catalysts based on spinel-type manganese-cobalt oxide nanofibres fabricated by an electrospinning technique. The spinel oxide nanofibres exhibit high catalytic activity towards both oxygen reduction and evolution in an alkaline electrolyte. When incorporated as cathode catalysts in Zn-air batteries, the fibrous spinel oxides considerably reduce the discharge-charge voltage gaps (improve the round-trip efficiency) in comparison to the catalyst-free cathode. Moreover, the nanofibre catalysts remain stable over the course of repeated discharge-charge cycling; however, carbon corrosion in the catalyst/carbon composite cathode degrades the cycling performance of the batteries.

  8. Traffic-related air pollution and alveolar nitric oxide in southern California children.

    PubMed

    Eckel, Sandrah P; Zhang, Zilu; Habre, Rima; Rappaport, Edward B; Linn, William S; Berhane, Kiros; Zhang, Yue; Bastain, Theresa M; Gilliland, Frank D

    2016-05-01

    Mechanisms for the adverse respiratory effects of traffic-related air pollution (TRAP) have yet to be established. We evaluated the acute effects of TRAP exposure on proximal and distal airway inflammation by relating indoor nitric oxide (NO), a marker of TRAP exposure in the indoor microenvironment, to airway and alveolar sources of exhaled nitric oxide (FeNO).FeNO was collected online at four flow rates in 1635 schoolchildren (aged 12-15 years) in southern California (USA) breathing NO-free air. Indoor NO was sampled hourly and linearly interpolated to the time of the FeNO test. Estimated parameters quantifying airway wall diffusivity (DawNO) and flux (J'awNO) and alveolar concentration (CANO) sources of FeNO were related to exposure using linear regression to adjust for potential confounders.We found that TRAP exposure indoors was associated with elevated alveolar NO. A 10 ppb higher indoor NO concentration at the time of the FeNO test was associated with 0.10 ppb higher average CANO (95% CI 0.04-0.16) (equivalent to a 7.1% increase from the mean), 4.0% higher J'awNO (95% CI -2.8-11.3) and 0.2% lower DawNO (95% CI -4.8-4.6).These findings are consistent with an airway response to TRAP exposure that was most marked in the distal airways. PMID:26797034

  9. Oxidation, volatilization, and redistribution of molybdenum from TZM alloy in air

    SciTech Connect

    Smolik, G.R.; Petti, D.A.; McCarthy, K.A.; Schuetz, S.T.

    2000-01-01

    The excellent high temperature strength and thermal conductivity of molybdenum-base alloys provide attractive features for components in advanced magnetic and inertial fusion devices. Refractory metal alloys react readily with oxygen and other gases. Oxidized molybdenum in turn is susceptible to losses from volatile molybdenum trioxide species, MoO{sub 3}(m), in air and the hydroxide, MoO{sub 2}(OH){sub 2}, formed from water vapor. Transport of radioactivity by the volatilization, migration, and re-deposition of these volatile species during a potential accident involving a loss of vacuum or inert environment represents a safety issue. In this report the authors present experimental results on the oxidation, volatilization and re-deposition of molybdenum from TZM in flowing air between 400 and 800 C. These results are compared with calculations obtained from a vaporization mass transfer model using chemical thermodynamic data for vapor pressures of MoO{sub 3}(g) over pure solid MoO{sub 3} and an expression for the vapor pressures of MoO{sub 2}(OH){sub 2} from the literature. Calculations correlate well with experimental data.

  10. Oxidation, Volatilization, and Redistribution of Molybdenum from TZM Alloy in Air

    SciTech Connect

    Smolik, Galen Richard; Petti, David Andrew; Mccarthy, Kathryn Ann; Schuetz, Stanley Thomas

    2000-01-01

    The excellent high temperature strength and thermal conductivity of molybdenum-base alloys provide attractive features for components in advanced magnetic and inertial fusion devices. Refractory metal alloys react readily with oxygen and other gases. Oxidized molybdenum in turn is susceptible to losses from volatile molybdenum trioxide species, (MoO3)m, in air and the hydroxide, MoO2(OH)2, formed from water vapor. Transport of radioactivity by the volatilization, migration, and re-deposition of these volatile species during a potential accident involving a loss of vacuum or inert environment represents a safety issue. In this report we present experimental results on the oxidation, volatilization and re-deposition of molybdenum from TZM in flowing air between 400 and 800°C. These results are compared with calculations obtained from a vaporization mass transfer model using chemical thermodynamic data for vapor pressures of MoO3(g) over pure solid MoO3 and an expression for the vapor pressures of MoO2(OH)2 from the literature. Calculations correlate well with experimental data.

  11. Novel Molten Oxide Membrane for Ultrahigh Purity Oxygen Separation from Air.

    PubMed

    Belousov, Valery V; Kulbakin, Igor V; Fedorov, Sergey V; Klimashin, Anton A

    2016-08-31

    We present a novel solid/liquid Co3O4-36 wt % Bi2O3 composite that can be used as molten oxide membrane, MOM ( Belousov, V. V. Electrical and Mass Transport Processes in Molten Oxide Membranes. Ionics 22 , 2016 , 451 - 469 ), for ultrahigh purity oxygen separation from air. This membrane material consists of Co3O4 solid grains and intergranular liquid channels (mainly molten Bi2O3). The solid grains conduct electrons, and the intergranular liquid channels predominantly conduct oxygen ions. The liquid channels also provide the membrane material gas tightness and ductility. This last property allows us to deal successfully with the problem of thermal incompatibility. Oxygen and nitrogen permeation fluxes, oxygen ion transport number, and conductivity of the composite were measured by the gas flow, volumetric measurements of the faradaic efficiency, and four-probe dc techniques, accordingly. The membrane material showed the highest oxygen selectivity jO2/jN2 > 10(5) and sufficient oxygen permeability 2.5 × 10(-8) mol cm(-1) s(-1) at 850 °C. In the range of membrane thicknesses 1.5-3.3 mm, the oxygen permeation rate was controlled by chemical diffusion. The ease of the MOM fabrication, combined with superior oxygen selectivity and competitive oxygen permeability, shows the promise of the membrane material for ultrahigh purity oxygen separation from air. PMID:27482771

  12. Increasing the Upper Temperature Oxidation Limit of Alumina Forming Austenitic Stainless Steels in Air with Water Vapor

    SciTech Connect

    Brady, Michael P; Unocic, Kinga A; Lance, Michael J; Santella, Michael L; Yamamoto, Yukinori; Walker, Larry R

    2011-01-01

    A family of alumina-forming austenitic (AFA) stainless steels is under development for use in aggressive oxidizing conditions from {approx}600-900 C. These alloys exhibit promising mechanical properties but oxidation resistance in air with water vapor environments is currently limited to {approx}800 C due to a transition from external protective alumina scale formation to internal oxidation of aluminum with increasing temperature. The oxidation behavior of a series of AFA alloys was systematically studied as a function of Cr, Si, Al, C, and B additions in an effort to provide a basis to increase the upper-temperature oxidation limit. Oxidation exposures were conducted in air with 10% water vapor environments from 800-1000 C, with post oxidation characterization of the 900 C exposed samples by electron probe microanalysis (EPMA), scanning and transmission electron microscopy, and photo-stimulated luminescence spectroscopy (PSLS). Increased levels of Al, C, and B additions were found to increase the upper-temperature oxidation limit in air with water vapor to between 950 and 1000 C. These findings are discussed in terms of alloy microstructure and possible gettering of hydrogen from water vapor at second phase carbide and boride precipitates.

  13. Vacuum-arc chromium-based coatings for protection of zirconium alloys from the high-temperature oxidation in air

    NASA Astrophysics Data System (ADS)

    Kuprin, A. S.; Belous, V. A.; Voyevodin, V. N.; Bryk, V. V.; Vasilenko, R. L.; Ovcharenko, V. D.; Reshetnyak, E. N.; Tolmachova, G. N.; V'yugov, P. N.

    2015-10-01

    Multilayer Cr-Zr/Cr/Cr-N coatings for protection of zirconium alloys from the high-temperature oxidation in air have been obtained by the vacuum-arc evaporation technique with application of filters for plasma cleaning from macroparticles. The effect of the coatings on the corrosion resistance of zirconium alloys at test temperatures between 660 and 1100 °C for 3600 s has been investigated. The thickness, structure, phase composition, mechanical properties of the coatings and oxide layers before and after oxidation tests were examined by scanning electron microscopy, X-ray diffraction analysis and nanoindentation technique. It is shown that the hard multilayer coating effectively protects zirconium from the oxidation in air for 1 h at test temperatures. As a result of the oxidation in the coating the CrO and Cr2O3 oxides are formed which reduce the oxygen penetration through the coating. At maximum test temperature of 1100 °C the oxide layer thickness in the coating is about 5 μm. The tube shape remains unchanged independent of alloy type. It has been found that uncoated zirconium oxidizes rapidly throughout the temperature range under study. At 1100 °C a porous monoclinic ZrO2 oxide layer of ≥120 μm is formed that leads to the deformation of the samples, cracking and spalling of the oxide layer.

  14. Nanoscale metal oxide and supported metal catalysts for Li-air battery

    NASA Astrophysics Data System (ADS)

    Huang, Kan

    The dissertation work focuses on research and development of durable nanoscale catalysts and supports for rechargeable Li-air batteries that use aqueous catholytes. Transition metal oxides, TiO2 and Nb2 O5 in particular, were prepared from a sol-gel process in the form of nanocoatings (5˜50 nm) on carbon nanotubes (CNTs) and studied as catalyst supports. Carbon doping in the oxides and post annealing significantly increased their electronic conductivity. Pt catalyst on the support with TiO 2 (Pt/c-TiO2/CNTs) showed a much better oxygen reduction reaction (ORR) activity than a commercial Pt on carbon black (Pt/C). Negligible loss (< 3%) in ORR activity was found in Pt/c-TiO2/CNTs as compared to more than 50% loss in Pt/C, demonstrating a significantly improved durability in the developed catalysts. However, Pt/c-Nb2O5/CNTs was found to be worse in ORR activity and durability, suggesting that c-Nb 2O5/CNTs may not be a good support. CNTs have fibrous shape and would provide a unique porous structure as electrode. Their buckypapers were made and used to support catalysts of Pt and IrO2 in the cathodes of Li-air batteries with sulfuric acid catholyte. At low Pt loading (5 wt.%) without IrO2 on the buckypaper cathode, the Li-air cell achieved a discharging capacity of 306 mAh/g and a specific energy of 1067 Wh/kg at 0.2 mA/cm2. A significant charge overpotential reduction (˜ 0.3 V) was achieved when IrO2 was also used to form a bifunctional catalyst with Pt on the buckypapers. The round trip efficiency was increased from 72% to 81% with the bifunctional cathode, demonstrating a higher energy conversion efficiency.

  15. Soil air carbon dioxide and nitrous oxide concentrations in profiles under tallgrass prairie and cultivation

    SciTech Connect

    Sotomayor, D.; Rice, C.W.

    1999-05-01

    Assessing the dynamics of gaseous production in soils is of interest because they are important sources and sinks of greenhouse gases. Changes in soil air carbon dioxide (CO{sub 2}) and nitrous oxide (N{sub 2}O) concentrations were studied in a Reading silt loam under prairie and cultivation. Concentrations were measured in situ over a 17-mo period to a depth of 3 m. Multilevel samples permitted collection of gases with subsequent measurement by gas chromatography in the laboratory. Soil air N{sub 2}O concentrations were near atmospheric levels for a majority of the study period in the prairie site but were significantly higher in the cultivated site. Annual mean N{sub 2}O concentrations were 0.403 and 1.09 {micro}L L{sup {minus}1} in the prairie and cultivated sites, respectively. Soil air CO{sub 2} annual mean concentrations were 1.56 {times} 10{sup 4} and 1.10 {times} 10{sup 4} {micro}L L{sup {minus}1} and ranged from 0.096 {times} 10{sup 4} to 6.45 {times} 10{sup 4} {micro}L L{sup {minus}1} and 0.087 {times} 10{sup 4} to 3.59 {times} 10{sup 4} {micro}L L{sup {minus}1} in the prairie and cultivated sites, respectively. Concentrations generally increased with depth, with maximum soil air N{sub 2}O and CO{sub 2} concentrations at 1.0 m in the prairie site and 0.5 m in the cultivated site. Nitrous oxide in the cultivated site and CO{sub 2} at both sites did not change markedly over winter months, but CO{sub 2} and N{sub 2}O concentrations reached maximums during the summer months and decreased as the year progressed. Although soil air concentrations peaked and decreased faster at shallower depths, deeper depths exhibited relative maximum concentrations for longer time periods.

  16. Treatment of biomass gasification wastewater using a combined wet air oxidation/activated sludge process

    SciTech Connect

    English, C.J.; Petty, S.E.; Sklarew, D.S.

    1983-02-01

    A lab-scale treatability study for using thermal and biological oxidation to treat a biomass gasification wastewater (BGW) having a chemical oxygen demand (COD) of 46,000 mg/l is described. Wet air oxidation (WA0) at 300/sup 0/C and 13.8 MPa (2000 psi) was used to initially treat the BGW and resulted in a COD reduction of 74%. This was followed by conventional activated sludge treatment using operating conditions typical of municipal sewage treatment plants. This resulted in an additional 95% COD removal. Overall COD reduction for the combined process was 99%. A detailed chemical analysis of the raw BGW and thermal and biological effluents was performed using gas chromatography/mass spectrometry (GC/MS). These results showed a 97% decrease in total extractable organics with WA0 and a 99.6% decrease for combined WA0 and activated sludge treatment. Components of the treated waters tended to be fewer in number and more highly oxidized. An experiment was conducted to determine the amount of COD reduction caused by volatilization during biological treatment. Unfortunately, this did not yield conclusive results. Treatment of BGW using WA0 followed by activated sludge appears to be very effective and investigations at a larger scale are recommended.

  17. Treatment of desizing wastewater containing poly(vinyl alcohol) by wet air oxidation

    SciTech Connect

    Chen, G.; Lei, L.; Yue, P.L.; Cen, P.

    2000-05-01

    The effectiveness of wet air oxidation (WAO) is studied in a 2-L autoclave for the treatment of desizing wastewater from man-made fiber textile plants. At an oxygen pressure of less than 2 MPa, over 30-min, chemical oxygen demand (COD) removal was found to increase from 15 to 65% when the temperature was raised from 150 to 250 C. The biodegradability of the wastewater was also simultaneously increased. Up to 90% of the COD could be removed within 120 min. A simplified reaction mechanism is proposed which involves a direct mineralization step in parallel with a step in which an intermediate is formed prior to mineralization. A kinetic model for COD removal was developed based on this reaction mechanism. The model was tested with experimental COD results over the temperature range of the experiments. The dependence of the specific reaction rate constants was found to follow the Arrhenius type of equation. The direct oxidation of poly(vinyl alcohol) (PVA) to carbon dioxide and water is the dominant reaction step. The intermediates formed are not likely to be the acetic acid but may be short segments of PVA that are easily oxidized.

  18. Oxidation Resistance of Materials Based on Ti3AlC2 Nanolaminate at 600 °C in Air

    NASA Astrophysics Data System (ADS)

    Ivasyshyn, Andrij; Ostash, Orest; Prikhna, Tatiana; Podhurska, Viktoriya; Basyuk, Tatiana

    2016-08-01

    The oxidation behavior of Ti3AlC2-based materials had been investigated at 600 °C in static air for 1000 h. It was shown that the intense increase of weight gain per unit surface area for sintered material with porosity of 22 % attributed to oxidation of the outer surface of the specimen and surfaces of pores in the bulk material. The oxidation kinetics of the hot-pressed Ti3AlC2-based material with 1 % porosity remarkably increased for the first 15 h and then slowly decreased. The weight gain per unit surface area for this material was 1.0 mg/cm2 after exposition for 1000 h. The intense initial oxidation of Ti3AlC2-based materials can be eliminated by pre-oxidation treatment at 1200 °C in air for 2 h. As a result, the weight gain per unit surface area for the pre-oxidized material did not exceed 0.11 mg/cm2 after 1000 h of exposition at 600 °C in air. It was demonstrated that the oxidation resistance of Ti3AlC2-based materials can be significantly improved by niobium addition.

  19. Secondary Organic Aerosol Formation from Ambient Air in an Oxidation Flow Reactor at GoAmazon2014/5

    NASA Astrophysics Data System (ADS)

    Palm, Brett B.; de Sa, Suzane S.; Campuzano-Jost, Pedro; Day, Douglas A.; Hu, Weiwei; Seco, Roger; Park, Jeong-Hoo; Guenther, Alex; Kim, Saewung; Brito, Joel; Wurm, Florian; Artaxo, Paulo; Yee, Lindsay; Isaacman-VanWertz, Gabrial; Goldstein, Allen; Newburn, Matt K.; Lizabeth Alexander, M.; Martin, Scot T.; Brune, William H.; Jimenez, Jose L.

    2016-04-01

    During GoAmazon2014/5, ambient air was exposed to controlled concentrations of OH or O3 in situ using an oxidation flow reactor (OFR). Oxidation ranged from hours-several weeks of aging. Oxidized air was sampled by several instruments (e.g., HR-AMS, ACSM, PTR-TOF-MS, SMPS, CCN) at both the T3 site (IOP1: Feb 1-Mar 31, 2014, and IOP2: Aug 15-Oct 15, 2014) and T2 site (between IOPs and into 2nd IOP). The oxidation of ambient air in the OFR led to substantial and variable secondary organic aerosol (SOA) formation from any SOA-precursor gases, known and unknown, that entered the OFR. In general, more SOA was produced during the nighttime than daytime, suggesting that SOA-precursor gases were found in relatively higher concentrations at night. Similarly, more SOA was formed in the dry season (IOP2) than wet season (IOP1). The maximum amount of SOA produced during nighttime from OH oxidation ranged from less than 1 μg/m3 on some nights to greater than 10 μg/m3 on other nights. O3 oxidation of ambient air also led to SOA formation, although several times less than from OH oxidation. The amount of SOA formation sometimes, but not always, correlated with measured gas-phase biogenic and/or anthropogenic SOA precursors (e.g., SV-TAG sesquiterpenes, PTR-TOFMS aromatics, isoprene, and monoterpenes). The SOA mass formed in the OFR from OH oxidation was up to an order of magnitude larger than could be explained from aerosol yields of measured primary VOCs. This along with measurements from previous campaigns suggests that most SOA was formed from intermediate S/IVOC sources (e.g., VOC oxidation products, evaporated POA, or direct emissions). To verify the SOA yields of VOCs under OFR experimental conditions, atmospherically-relevant concentrations of several VOCs were added individually into ambient air in the OFR and oxidized by OH or O3. SOA yields in the OFR were similar to published chamber yields. Preliminary PMF factor analysis showed production of secondary factors in

  20. High temperature silver-palladium-copper oxide air braze filler metal

    NASA Astrophysics Data System (ADS)

    Darsell, Jens Tommy

    The Ag-CuO system is currently being investigated as the basis for an air braze filler metal alloy to be used in SOFC components. The system is of interest because unlike most braze alloys, it is capable of wetting a variety of ceramic materials while being applied in an air. This thesis work examined modification of Ag-CuO filler metal system by alloying with palladium to increase the use temperature of the resulting air braze alloy. Thermal analysis was performed to track changes in the solidus and liquidus temperatures for these alloys and determine equilibrium phase present as a function of temperature and composition. Sessile drop experiments were performed to investigate the effect of palladium addition on braze wetability. The influence of copper-oxide and palladium contents on brazed joint strength was characterized by a combination of four-point bend testing and fractography. From combined thermal analysis and quenched data it was found that both the liquidus and solidus increase with increasing palladium content, and the silver-rich miscibility gap boundary could be shifted by the addition of palladium. This was employed as a tool to study the effects of two-liquid phase formation on wetting behavior. In addition, a mass loss likely attributable to silver volatilization is observed in the Pd-modified filler metals when heated over ˜1100°C. As volatilization should be avoided, the ternary alloys should be limited to 15mol% Pd. It was found by sessile drop wetting experiments that there is a definitive change in wetting behavior that corresponds directly to the miscibility gap boundary for the Pd-Ag-CuO system. The first order transition tracks with changes in the miscibility gap boundary that can be induced by increasing palladium content. This is the first experimental evidence of critical point wetting behavior reported for a metal-oxide system and further confirms that critical point wetting theory is universal. Four-point bend testing and

  1. FINAL REPORT on Experimental Validation of Stratified Flow Phenomena, Graphite Oxidation, and Mitigation Strategies of Air Ingress Accidents

    SciTech Connect

    Chang H. Oh; Eung S. Kim; Hee C. NO; Nam Z. Cho

    2011-01-01

    The U.S. Department of Energy is performing research and development that focuses on key phenomena that are important during challenging scenarios that may occur in the Next Generation Nuclear Plant (NGNP)/Generation IV very high temperature reactor (VHTR). Phenomena Identification and Ranking studies to date have identified the air ingress event, following on the heels of a VHTR depressurization, as very important. Consequently, the development of advanced air ingress-related models and verification & validation are of very high priority for the NGNP Project. Following a loss of coolant and system depressurization incident, air ingress will occur through the break, leading to oxidation of the in-core graphite structure and fuel. This study indicates that depending on the location and the size of the pipe break, the air ingress phenomena are different. In an effort to estimate the proper safety margin, experimental data and tools, including accurate multidimensional thermal-hydraulic and reactor physics models, a burn-off model, and a fracture model are required. It will also require effective strategies to mitigate the effects of oxidation, eventually. This 3-year project (FY 2008–FY 2010) is focused on various issues related to the VHTR air-ingress accident, including (a) analytical and experimental study of air ingress caused by density-driven, stratified, countercurrent flow, (b) advanced graphite oxidation experiments, (c) experimental study of burn-off in the core bottom structures, (d) structural tests of the oxidized core bottom structures, (e) implementation of advanced models developed during the previous tasks into the GAMMA code, (f) full air ingress and oxidation mitigation analyses, (g) development of core neutronic models, (h) coupling of the core neutronic and thermal hydraulic models, and (i) verification and validation of the coupled models.

  2. Oxidation rate of nuclear-grade graphite IG-110 in the kinetic regime for VHTR air ingress accident scenarios

    NASA Astrophysics Data System (ADS)

    Lee, Jo Jo; Ghosh, Tushar K.; Loyalka, Sudarshan K.

    2014-03-01

    The oxidation rates of nuclear-grade graphite IG-110 in the kinetically-controlled temperature regime of graphite oxidation were predicted and compared in Very High Temperature Reactor air ingress accident scenarios. The oxidative mass loss of graphite was measured thermogravimetrically from 873 to 1873 K in 100% air (21 mol%). The activation energy was found to be 222.07 kJ/mol, and the order of reaction with respect to oxygen concentration is 0.76. The surfaces of the samples were characterized by Scanning Electron Microscopy, Energy Dispersive Spectroscopy, Fourier Transform Infrared Spectroscopy and X-ray Photoelectron Spectroscopy before and after oxidation. These results are compared with those available in the literature, and our recently reported results for NBG-18 nuclear-grade graphite using the same technique.

  3. Decomposition of nitric oxide in a hot nitrogen stream to synthesize air for hypersonic wind tunnel combustion testing

    NASA Technical Reports Server (NTRS)

    Zumdieck, J. F.; Zlatarich, S. A.

    1974-01-01

    A clean source of high enthalpy air was obtained from the exothermic decomposition of nitric oxide in the presence of strongly heated nitrogen. A nitric oxide jet was introduced into a confined coaxial nitrogen stream. Measurements were made of the extent of mixing and reaction. Experimental results are compared with one- and two-dimensional chemical kinetics computations. Both analyses predict much lower reactivity than was observed experimentally. Inlet nitrogen temperatures above 2400 K were sufficient to produce experimentally a completely reacted gas stream of synthetic air.

  4. The NASA Lightning Nitrogen Oxides Model (LNOM): Application to Air Quality Modeling

    NASA Technical Reports Server (NTRS)

    Koshak, William; Peterson, Harold; Khan, Maudood; Biazar, Arastoo; Wang, Lihua

    2011-01-01

    Recent improvements to the NASA Marshall Space Flight Center Lightning Nitrogen Oxides Model (LNOM) and its application to the Community Multiscale Air Quality (CMAQ) modeling system are discussed. The LNOM analyzes Lightning Mapping Array (LMA) and National Lightning Detection Network(TradeMark)(NLDN) data to estimate the raw (i.e., unmixed and otherwise environmentally unmodified) vertical profile of lightning NO(x) (= NO + NO2). The latest LNOM estimates of lightning channel length distributions, lightning 1-m segment altitude distributions, and the vertical profile of lightning NO(x) are presented. The primary improvement to the LNOM is the inclusion of non-return stroke lightning NOx production due to: (1) hot core stepped and dart leaders, (2) stepped leader corona sheath, K-changes, continuing currents, and M-components. The impact of including LNOM-estimates of lightning NO(x) for an August 2006 run of CMAQ is discussed.

  5. Wear and friction of oxidation-resistant mechanical carbon graphites at 650 C in air

    NASA Technical Reports Server (NTRS)

    Allen, G. P.; Wisnader, D. W.

    1975-01-01

    Studies were conducted to determine the friction and wear properties of experimental carbon-graphites. Hemispherically tipped carbon-graphite rider specimens were tested in sliding contact with rotating Inconel X-750 disks in air. A surface speed of 1.33 m/sec, a load of 500 g, and a specimen temperature of 650 C were used. Results indicate: (1) hardness is not a major factor in determining friction and wear under the conditions of these studies. (2) Friction and wear as low as or lower than those observed for a good commercial seal material were attained with some of the experimental materials studied. (3) The inclusion of boron carbide (as an oxidation inhibitor) has a strong influence on wear rate. (4) Phosphate treatment reduces the friction coefficient when boron carbide is not present in the base material.

  6. Investigation of hydrogen-air ignition sensitized by nitric oxide and by nitrogen dioxide

    NASA Technical Reports Server (NTRS)

    Slack, M.; Grillo, A.

    1977-01-01

    The sensitization of stoichiometric hydrogen-air ignition by NO, NO2 and a mixture of NO and NO2 was investigated behind reflected shock waves in a shock tube. Induction times were measured in pressure range 0.27 to 2.0 atm, temperature range 800 to 1500 K, and for NO or NO2 mole percent between 0.0 and 4.5. Addition of both NO and NO2 reduced the measured induction times. The experimental data are interpreted in terms of H2-O2-NO(x) oxidation reaction mechanisms. The influence of NO(x) upon a supersonic combustion ramjet combustor test, conducted in an arc-heated facility, is assessed.

  7. Homogeneous catalytic wet-air oxidation for the treatment of textile wastewater

    SciTech Connect

    Lei, L. Chen, G.; Hu, X.; Yue, P.L.

    2000-04-01

    An extensive series of experiments was performed to identify suitable catalysts to increase the reaction rate of wet-air oxidation of textile wastewater t relatively mild temperatures an pressures. Wastewater types treated included natural-fiber desizing wastewater, synthetic-fiber desizing wastewater, and printing and dyeing wastewater. Experimental results indicated that all catalysts tested in this investigation significantly increased the chemical oxygen demand (COD) and total organic carbon (TOC) removal rates and total COD and TOC removals. Of all catalysts tested, copper salts were the most effective. Anions in the slat solutions played a role in the catalytic process. Nitrate ions were more effective than sulfate ions. Similarly, copper nitrates were more effective than copper sulfates. A mixture of salts containing different metals performed better than any single salt.

  8. Air/water oxidative desulfurization of coal and sulfur-containing compounds

    NASA Astrophysics Data System (ADS)

    Warzinski, R. P.; Freidman, S.; LaCount, R. B.

    1981-02-01

    Air/water Oxydesulfurization has been demonstrated in autoclave experiments at the Pittsburgh Energy Technology Center for various coals representative of the major U. S. coal basins. The applicability at present of this treatment for producing an environmentally acceptable coal has been restricted by recently proposed SO2 emission standards for utility boilers. The product would, however, be attractive to the many smaller industrial coal users who cannot afford to operate and maintain flue gas desulfurization systems. It is also possible that the utility industry could realize a benefit by using chemically cleaned coal with partial flue gas scrubbing. The higher cost of the cleaned coal would be offset by the reduction in capital and operating costs resulting from decreased FGD requirements. The susceptibility of sulfur in coal to oxidative removal varies with the nature of the sulfur-containing species. The inorganic sulfur compounds, primarily pyrite, marcasite, and iron sulfate, are more amenable to treatment than the organically bound sulfur which exhibits varying degrees of resistance depending on its chemical environment. Air/water Oxydesulfurization consistently removes in excess of 90 percent of the pyritic sulfur; the extent and efficiency of organic sulfur removal however, depends on the type of coal and severity of treatment used. In general, the organic sulfur of the higher rank coals exhibits more resistance to treatment than that of the lower rank coals; however, the accompanying heating value is greater for the latter. Similar treatment of sulfur-containing model compounds further illustrates the relative susceptibilities of different chemical species to oxidation. Application of these data to the understanding of the complex chemistry involved in the treatment of coal is a preliminary step toward improving the efficiency of Oxydesulfurization.

  9. Nitrous oxide supersaturation at the liquid/air interface of animal waste.

    PubMed

    Makris, Konstantinos C; Andra, Syam S; Hardy, Michael; Sarkar, Dibyendu; Datta, Rupali; Bach, Stephan B H; Mullens, Conor P

    2009-12-01

    Concentrated animal feeding operations around the globe generate large amounts of nitrous oxide (N(2)O) in the surrounding atmosphere. Liquid animal waste systems have received little attention with respect to N(2)O emissions. We hypothesized that the solution chemistry of animal waste aqueous suspensions would promote conditions that lead to N(2)O supersaturation at the liquid/air interface. The concentration of dissolved N(2)O in poultry litter (PL) aqueous suspensions at 25 degrees C was 0.36 microg N(2)O mL(-1), at least an order of magnitude greater than that measured in water in equilibrium with ambient air, suggesting N(2)O supersaturation. There was a nonlinear increase in the N(2)O Henry constants of PL from 2810 atm/mole fraction at 35 degrees C to 17 300 atm/mole fraction at 41 degrees C. The extremely high N(2)O Henry constants were partially ascribed to N(2)O complexation with aromatic moieties. Complexed N(2)O structures were unstable at temperatures > 35 degrees C, supplying the headspace with additional free N(2)O concentrations. PMID:19573962

  10. A new class of solid oxide metal-air redox batteries for advanced stationary energy storage

    NASA Astrophysics Data System (ADS)

    Zhao, Xuan

    Cost-effective and large-scale energy storage technologies are a key enabler of grid modernization. Among energy storage technologies currently being researched, developed and deployed, rechargeable batteries are unique and important that can offer a myriad of advantages over the conventional large scale siting- and geography- constrained pumped-hydro and compressed-air energy storage systems. However, current rechargeable batteries still need many breakthroughs in material optimization and system design to become commercially viable for stationary energy storage. This PhD research project investigates the energy storage characteristics of a new class of rechargeable solid oxide metal-air redox batteries (SOMARBs) that combines a regenerative solid oxide fuel cell (RSOFC) and hydrogen chemical-looping component. The RSOFC serves as the "electrical functioning unit", alternating between the fuel cell and electrolysis mode to realize discharge and charge cycles, respectively, while the hydrogen chemical-looping component functions as an energy storage unit (ESU), performing electrical-chemical energy conversion in situ via a H2/H2O-mediated metal/metal oxide redox reaction. One of the distinctive features of the new battery from conventional storage batteries is the ESU that is physically separated from the electrodes of RSOFC, allowing it to freely expand and contract without impacting the mechanical integrity of the entire battery structure. This feature also allows an easy switch in the chemistry of this battery. The materials selection for ESU is critical to energy capacity, round-trip efficiency and cost effectiveness of the new battery. Me-MeOx redox couples with favorable thermodynamics and kinetics are highly preferable. The preliminary theoretical analysis suggests that Fe-based redox couples can be a promising candidate for operating at both high and low temperatures. Therefore, the Fe-based redox-couple systems have been selected as the baseline for this

  11. Intrinsic catalytic properties of extruded clay honeycomb monolith toward complete oxidation of air pollutants.

    PubMed

    Assebban, Mhamed; El Kasmi, Achraf; Harti, Sanae; Chafik, Tarik

    2015-12-30

    The present work highlights the intrinsic catalytic properties of extruded clay honeycomb monolith toward complete oxidation of various air pollutants namely CO, methane, propane, acetylene, propene, n-butene, methanol, ethanol, n-propanol, n-butanol, acetone, dimethyl ether, benzene, toluene, o-xylene, monochlorobenzene and 1,2-dichlorobenzene. Total catalytic conversion was achieved for all tested compounds with different behaviors depending on pollutants' structural and chemical nature. The comparison of T50 values obtained from light-off curves allowed the establishment of the following reactivity sequence: ketone>alcohol>ether>CO>alkyne>aromatic>alkene>chlorinated aromatic>alkane. The intrinsic catalytic performances of the natural clay was ascribed to the implication of a quite complex mixture constituted by OH groups (Brønsted acids) and coordinately-unsaturated cations, such as Al(3+), Fe(3+) and Fe(2+) (Lewis acids). Hence, the combination of the clay's intrinsic catalytic performances and easier extrudability suggests a promissory potential for application in air pollution control. PMID:26259164

  12. Disrupted Nitric Oxide Metabolism from Type II Diabetes and Acute Exposure to Particulate Air Pollution

    PubMed Central

    Pettit, Ashley P.; Kipen, Howard; Laumbach, Robert; Ohman-Strickland, Pamela; Kelly-McNeill, Kathleen; Cepeda, Clarimel; Fan, Zhi-Hua; Amorosa, Louis; Lubitz, Sara; Schneider, Stephen; Gow, Andrew

    2015-01-01

    Type II diabetes is an established cause of vascular impairment. Particulate air pollution is known to exacerbate cardiovascular and respiratory conditions, particularly in susceptible populations. This study set out to determine the impact of exposure to traffic pollution, with and without particle filtration, on vascular endothelial function in Type II diabetes. Endothelial production of nitric oxide (NO) has previously been linked to vascular health. Reactive hyperemia induces a significant increase in plasma nitrite, the proximal metabolite of NO, in healthy subjects, while diabetics have a lower and more variable level of response. Twenty type II diabetics and 20 controls (ages 46–70 years) were taken on a 1.5hr roadway traffic air pollution exposure as passengers. We analyzed plasma nitrite, as a measure of vascular function, using forearm ischemia to elicit a reactive hyperemic response before and after exposure to one ride with and one without filtration of the particle components of pollution. Control subjects displayed a significant increase in plasma nitrite levels during reactive hyperemia. This response was no longer present following exposure to traffic air pollution, but did not vary with whether or not the particle phase was filtered out. Diabetics did not display an increase in nitrite levels following reactive hyperemia. This response was not altered following pollution exposure. These data suggest that components of acute traffic pollution exposure diminish vascular reactivity in non-diabetic individuals. It also confirms that type II diabetics have a preexisting diminished ability to appropriately respond to a vascular challenge, and that traffic pollution exposure does not cause a further measureable acute change in plasma nitrite levels in Type II diabetics. PMID:26656561

  13. Producing nitric oxide by pulsed electrical discharge in air for portable inhalation therapy.

    PubMed

    Yu, Binglan; Muenster, Stefan; Blaesi, Aron H; Bloch, Donald B; Zapol, Warren M

    2015-07-01

    Inhalation of nitric oxide (NO) produces selective pulmonary vasodilation and is an effective therapy for treating pulmonary hypertension in adults and children. In the United States, the average cost of 5 days of inhaled NO for persistent pulmonary hypertension of the newborn is about $14,000. NO therapy involves gas cylinders and distribution, a complex delivery device, gas monitoring and calibration equipment, and a trained respiratory therapy staff. The objective of this study was to develop a lightweight, portable device to serve as a simple and economical method of producing pure NO from air for bedside or portable use. Two NO generators were designed and tested: an offline NO generator and an inline NO generator placed directly within the inspiratory line. Both generators use pulsed electrical discharges to produce therapeutic range NO (5 to 80 parts per million) at gas flow rates of 0.5 to 5 liters/min. NO was produced from air, as well as gas mixtures containing up to 90% O2 and 10% N2. Potentially toxic gases produced in the plasma, including nitrogen dioxide (NO2) and ozone (O3), were removed using a calcium hydroxide scavenger. An iridium spark electrode produced the lowest ratio of NO2/NO. In lambs with acute pulmonary hypertension, breathing electrically generated NO produced pulmonary vasodilation and reduced pulmonary arterial pressure and pulmonary vascular resistance index. In conclusion, electrical plasma NO generation produces therapeutic levels of NO from air. After scavenging to remove NO2 and O3 and filtration to remove particles, electrically produced NO can provide safe and effective treatment of pulmonary hypertension. PMID:26136478

  14. Improved air stability of perovskite solar cells via solution-processed metal oxide transport layers

    NASA Astrophysics Data System (ADS)

    You, Jingbi; Meng, Lei; Song, Tze-Bin; Guo, Tzung-Fang; Yang, Yang (Michael); Chang, Wei-Hsuan; Hong, Ziruo; Chen, Huajun; Zhou, Huanping; Chen, Qi; Liu, Yongsheng; De Marco, Nicholas; Yang, Yang

    2016-01-01

    Lead halide perovskite solar cells have recently attracted tremendous attention because of their excellent photovoltaic efficiencies. However, the poor stability of both the perovskite material and the charge transport layers has so far prevented the fabrication of devices that can withstand sustained operation under normal conditions. Here, we report a solution-processed lead halide perovskite solar cell that has p-type NiOx and n-type ZnO nanoparticles as hole and electron transport layers, respectively, and shows improved stability against water and oxygen degradation when compared with devices with organic charge transport layers. Our cells have a p-i-n structure (glass/indium tin oxide/NiOx/perovskite/ZnO/Al), in which the ZnO layer isolates the perovskite and Al layers, thus preventing degradation. After 60 days storage in air at room temperature, our all-metal-oxide devices retain about 90% of their original efficiency, unlike control devices made with organic transport layers, which undergo a complete degradation after just 5 days. The initial power conversion efficiency of our devices is 14.6 ± 1.5%, with an uncertified maximum value of 16.1%.

  15. Improved air stability of perovskite solar cells via solution-processed metal oxide transport layers.

    PubMed

    You, Jingbi; Meng, Lei; Song, Tze-Bin; Guo, Tzung-Fang; Yang, Yang Michael; Chang, Wei-Hsuan; Hong, Ziruo; Chen, Huajun; Zhou, Huanping; Chen, Qi; Liu, Yongsheng; De Marco, Nicholas; Yang, Yang

    2016-01-01

    Lead halide perovskite solar cells have recently attracted tremendous attention because of their excellent photovoltaic efficiencies. However, the poor stability of both the perovskite material and the charge transport layers has so far prevented the fabrication of devices that can withstand sustained operation under normal conditions. Here, we report a solution-processed lead halide perovskite solar cell that has p-type NiO(x) and n-type ZnO nanoparticles as hole and electron transport layers, respectively, and shows improved stability against water and oxygen degradation when compared with devices with organic charge transport layers. Our cells have a p-i-n structure (glass/indium tin oxide/NiO(x)/perovskite/ZnO/Al), in which the ZnO layer isolates the perovskite and Al layers, thus preventing degradation. After 60 days storage in air at room temperature, our all-metal-oxide devices retain about 90% of their original efficiency, unlike control devices made with organic transport layers, which undergo a complete degradation after just 5 days. The initial power conversion efficiency of our devices is 14.6 ± 1.5%, with an uncertified maximum value of 16.1%. PMID:26457966

  16. The oxidation behavior of a model molybdenum/tungsten-containing alloy in air alone and in air with trace levels of NaCl(g)

    NASA Technical Reports Server (NTRS)

    Smeggil, J. G.; Bornstein, N. S.

    1983-01-01

    Thermogravimetric, metallographic, and X-ray studies of a model alloy, Ni-(17 a/o)Al-(10 a/o)Mo+W, oxidized in dry air at 600-1200 C and in air with 10 ppm NaCl gas at 900 C, are reported. The alloy was melted under Ar and pretreated in flowing H2 for 24 h at 1300 C. Polished 1.3 x 1.3 x 0.2-cm specimens were washed and degreased prior to oxidation in a quartz tube within a furnace for up to 120 hr. The oxidation activation energy of the alloy is determined to be about 30 kcal/mole. The specimens oxidized at 900 C and hotter exhibited oxidized and nitrided phases covered by complex NiMoO4, NiWO4, and NiAl2O4 scales and a porous, nonprotective outer layer of NiO. The oxidation behavior is found to be determined by the formation and growth of the scale, especially the (Mo,W)O2 component. Al2O3 scale layers were not formed, and further runs with pure O2 or Ar-(20 percent)O2 ruled out an explanation of this phenomenon based on aluminum nitride formation. The oxidation was accelerated by the addition of NaCl gas, a finding attributed to the reaction of NaCl with external locally protective Al2O3 scales and with the internal(Mo, W)O2 layers.

  17. Biomarkers of occupational exposure to air pollution, inflammation and oxidative damage in taxi drivers.

    PubMed

    Brucker, Natália; Moro, Angela M; Charão, Mariele F; Durgante, Juliano; Freitas, Fernando; Baierle, Marília; Nascimento, Sabrina; Gauer, Bruna; Bulcão, Rachel P; Bubols, Guilherme B; Ferrari, Pedro D; Thiesen, Flávia V; Gioda, Adriana; Duarte, Marta M M F; de Castro, Iran; Saldiva, Paulo H; Garcia, Solange C

    2013-10-01

    Exposure to environmental pollutants has been recognised as a risk factor for cardiovascular events. 1-hydroxypyrene (1-OHP) is a biomarker of exposure to polycyclic aromatic hydrocarbons (PAHs) from traffic-related air pollution. Experimental studies indicate that PAH exposure could be associated with inflammation and atherogenesis. Thus, the purpose of this study was to evaluate whether the biomarker of PAH exposure is associated with biomarkers of inflammation and oxidative stress and if these effects modulate the risk of developing cardiovascular diseases in workers exposed to air pollution. This study included 60 subjects, comprising 39 taxi drivers and 21 non-occupationally exposed persons. Environmental PM2.5 and benzo[a]pyrene (BaP) levels, in addition to biomarkers of exposure and oxidative damage, were determined. Inflammatory cytokines (IL-1β, IL-6, IL-10, TNF-α, IFN-γ and hs-CRP) and serum levels of oxidised LDL (ox-LDL), auto-antibodies (ox-LDL-Ab) and homocysteine (Hcy) were also evaluated. PM2.5 and BaP exhibited averages of 12.4±6.9 μg m(-3) and 1.0±0.6 ng m(-3), respectively. Urinary 1-OHP levels were increased in taxi drivers compared to the non-occupationally exposed subjects (p<0.05) and were positively correlated with pro-inflammatory cytokines and negatively correlated with antioxidants. Furthermore, taxi drivers had elevated pro-inflammatory cytokines, biomarkers of oxidative damage, and ox-LDL, ox-LDL-Ab and Hcy levels, although antioxidant enzymes were decreased compared to the non-occupationally exposed subjects (p<0.05). In summary, our findings indicate that taxi drivers showed major exposure to pollutants, such as PAHs, in relation to non-occupationally exposed subjects. This finding was associated with higher inflammatory biomarkers and Hcy, which represent important predictors for cardiovascular events. These data suggest a contribution of PAHs to cardiovascular diseases upon occupational exposure. PMID:23872245

  18. Workshop in Support of the Secondary National Ambient Air Quality Standards for Nitrogen (NOx) and Sulfur Oxides (SOx)

    EPA Science Inventory

    EPA is announcing a workshop to discuss policy-relevant science to Inform EPA’s "Review of the Secondary National Ambient Air Quality Standards (NAAQS) for Oxides of Nitrogen and Sulfur" report. The workshop is being organized by EPA’s Office of Research and Development’s, Nation...

  19. What Is Happening when the Blue Bottle Bleaches: An Investigation of the Methylene Blue-Catalyzed Air Oxidation of Glucose

    ERIC Educational Resources Information Center

    Anderson, Laurens; Wittkopp, Stacy M.; Painter, Christopher J.; Liegel, Jessica J.; Schreiner, Rodney; Bell, Jerry A.; Shakhashiri, Bassam Z.

    2012-01-01

    An investigation of the Blue Bottle Experiment, a well-known lecture demonstration reaction involving the dye-catalyzed air oxidation of a reducing sugar in alkaline solution, has delineated the sequence of reactions leading to the bleaching of the dye, the regeneration of color, and so forth. Enolization of the sugar is proposed as a key step in…

  20. Oxidation Behavior of Germanium- and/or Silicon-Bearing Near-α Titanium Alloys in Air

    NASA Astrophysics Data System (ADS)

    Kitashima, Tomonori; Yamabe-Mitarai, Yoko

    2015-06-01

    The effect of germanium (Ge) and/or silicon (Si) addition on the oxidation behavior of the near-α alloy Ti-5Al-2Sn-4Zr-2Mo was investigated in air at 973 K (700 °C). Ge addition decreased the oxidation resistance because of the formation of a Ge-rich layer in the substrate at the TiO2/substrate interface, enhancing Sn segregation at the interface. In addition, a small amount of Ge dissolved in the external Al2O3 layer. These results reduced the aluminum activity at the interface, suppressed the formation of Al2O3, and increased the diffusivity of oxygen in the oxide scales. The addition of 0.2 and 0.9 wt pct Si was beneficial for improving oxidation resistance. The effect of germanide and silicide precipitates in the matrix on the oxide growth process was also discussed.

  1. 75 FR 61486 - Review of the Secondary National Ambient Air Quality Standards for Oxides of Nitrogen and Oxides...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-10-05

    ... Standards for Oxides of Nitrogen and Oxides of Sulfur: Second External Review Draft (75 FR 57463, September... an atmospheric chemistry perspective as well as from an environmental effects perspective,...

  2. Oxidation Behavior of Mo-Si-B Alloys in Wet Air

    SciTech Connect

    M. Kramer; A. Thom; O. Degirmen; V. Behrani; M. Akinc

    2002-04-22

    Multiphase composite alloys based on the Mo-Si-B system are candidate materials for ultra-high temperature applications. In non load-bearing uses such as thermal barrier coatings or heat exchangers in fossil fuel burners, these materials may be ideally suited. The present work investigated the effect of water vapor on the oxidation behavior of Mo-Si-B phase assemblages. Three alloys were studied: Alloy 1 = Mo{sub 5}Si{sub 3}B{sub x} (T1)- MoSi{sub 2}- MoB, Alloy 2 = T1- Mo{sub 5}SiB{sub 2} (T2)- Mo{sub 3}Si, and Alloy 3 = Mo- T2- Mo{sub 3}Si. Tests were conducted at 1000 and 1100C in controlled atmospheres of dry air and wet air nominally containing 18, 55, and 150 Torr H{sub 2}O. The initial mass loss of each alloy was approximately independent of the test temperature and moisture content of the atmosphere. The magnitude of these initial losses varied according to the Mo content of the alloys. All alloys formed a continuous, external silica scale that protected against further mass change after volatilization of the initially formed MoO{sub 3}. All alloys experienced a small steady state mass change, but the calculated rates cannot be quantitatively compared due to statistical uncertainty in the individual mass measurements. Of particular interest is that Alloy 3, which contains a significant volume fraction of Mo metal, formed a protective scale. All alloys formed varying amounts of subscale Mo and MoO{sub 2}. This implies that oxygen transport through the external silica scale has been significantly reduced. For all alloys, water vapor accelerated the growth of a multiphase interlayer at the silica scale/unoxidized alloy interface. This interlayer is likely composed of fine Mo and MoO{sub 2} that is dispersed within a thin silica matrix. Alloy 3 was particularly sensitive to water accelerated growth of this interlayer. At 1100 C, the scale thickness after 300 hours increased from about 20 mm in dry air to nearly 100 mm in wet air.

  3. Atomic structure and thermophysical properties of molten silver-copper oxide air braze alloys

    NASA Astrophysics Data System (ADS)

    Hardy, John Steven

    The Ag-CuOx materials system is the basis for a family of filler alloys used in a recently developed ceramic-metal joining technique referred to as air brazing, which is a brazing process that can be carried out in ambient air rather than under the vacuum or inert to reducing gas conditions required for conventional brazing methods. This research was conducted to elucidate the atomic coordination and selected thermophysical properties of these materials as a function of temperature when they are in the salient liquid state in air, since this is when the critical steps of wetting and spreading occur in the joining process. A series of alloys was selected spanning the entire length of the phase diagram including the pure end members, Ag and CuOx; alloys that form the two constituent single phase liquids; and alloys for which the two liquid phases coexist in the miscibility gap of the phase diagram. The oxygen content of the liquid alloys in air was measured using thermogravimetry. The oxidative weight gain of 99.999% pure metallic precursors was measured while simultaneously accounting for the concurrent silver volatility using a method that was developed in the course of the study. The surface tension and mass density were measured using the maximum bubble pressure method. The number density was calculated based on the information gained from the oxygen content and mass density measurements. For compositions that were amenable to laser heating, containerless high energy x-ray scattering measurements of the liquid atomic coordination were performed using a synchrotron beamline, an aerodynamic levitator, and laser heating. For the remaining compositions x-ray scattering measurements were performed in a beamline-compatible furnace. The two liquid phases that form in this materials system have distinct atomic coordinations characterized by an average of nearly two-fold coordinated ionic metal-oxygen pairs in the CuOx-rich liquid and nearly eight-fold coordinated atomic

  4. Preparation, certification and interlaboratory analysis of workplace air filters spiked with high-fired beryllium oxide.

    PubMed

    Oatts, Thomas J; Hicks, Cheryl E; Adams, Amy R; Brisson, Michael J; Youmans-McDonald, Linda D; Hoover, Mark D; Ashley, Kevin

    2012-02-01

    Occupational sampling and analysis for multiple elements is generally approached using various approved methods from authoritative government sources such as the National Institute for Occupational Safety and Health (NIOSH), the Occupational Safety and Health Administration (OSHA) and the Environmental Protection Agency (EPA), as well as consensus standards bodies such as ASTM International. The constituents of a sample can exist as unidentified compounds requiring sample preparation to be chosen appropriately, as in the case of beryllium in the form of beryllium oxide (BeO). An interlaboratory study was performed to collect analytical data from volunteer laboratories to examine the effectiveness of methods currently in use for preparation and analysis of samples containing calcined BeO powder. NIST SRM(®) 1877 high-fired BeO powder (1100 to 1200 °C calcining temperature; count median primary particle diameter 0.12 μm) was used to spike air filter media as a representative form of beryllium particulate matter present in workplace sampling that is known to be resistant to dissolution. The BeO powder standard reference material was gravimetrically prepared in a suspension and deposited onto 37 mm mixed cellulose ester air filters at five different levels between 0.5 μg and 25 μg of Be (as BeO). Sample sets consisting of five BeO-spiked filters (in duplicate) and two blank filters, for a total of twelve unique air filter samples per set, were submitted as blind samples to each of 27 participating laboratories. Participants were instructed to follow their current process for sample preparation and utilize their normal analytical methods for processing samples containing substances of this nature. Laboratories using more than one sample preparation and analysis method were provided with more than one sample set. Results from 34 data sets ultimately received from the 27 volunteer laboratories were subjected to applicable statistical analyses. The observed

  5. Catechol oxidation by ozone and hydroxyl radicals at the air-water interface.

    PubMed

    Pillar, Elizabeth A; Camm, Robert C; Guzman, Marcelo I

    2014-12-16

    Anthropogenic emissions of aromatic hydrocarbons promptly react with hydroxyl radicals undergoing oxidation to form phenols and polyphenols (e.g., catechol) typically identified in the complex mixture of humic-like substances (HULIS). Because further processing of polyphenols in secondary organic aerosols (SOA) can continue mediated by a mechanism of ozonolysis at interfaces, a better understanding about how these reactions proceed at the air-water interface is needed. This work shows how catechol, a molecular probe of the oxygenated aromatic hydrocarbons present in SOA, can contribute interfacial reactive species that enhance the production of HULIS under atmospheric conditions. Reactive semiquinone radicals are quickly produced upon the encounter of 40 ppbv-6.0 ppmv O3(g) with microdroplets containing [catechol] = 1-150 μM. While the previous pathway results in the instantaneous formation of mono- and polyhydroxylated aromatic rings (PHA) and chromophoric mono- and polyhydroxylated quinones (PHQ), a different channel produces oxo- and dicarboxylic acids of low molecular weight (LMW). The cleavage of catechol occurs at the 1,2 carbon-carbon bond at the air-water interface through the formation of (1) an ozonide intermediate, (2) a hydroperoxide, and (3) cis,cis-muconic acid. However, variable [catechol] and [O3(g)] can affect the ratio of the primary products (cis,cis-muconic acid and trihydroxybenzenes) and higher order products observed (PHA, PHQ, and LMW oxo- and dicarboxylic acids). Secondary processing is confirmed by mass spectrometry, showing the production of crotonic, maleinaldehydic, maleic, glyoxylic, and oxalic acids. The proposed pathway can contribute precursors to aqueous SOA (AqSOA) formation, converting aromatic hydrocarbons into polyfunctional species widely found in tropospheric aerosols with light-absorbing brown carbon. PMID:25423038

  6. Diagnostic significance of nitric oxide concentrations in exhaled air from the airways in allergic rhinitis patients

    PubMed Central

    Krzych-Fałta, Edyta; Samoliński, Bolesław K; Zalewska, Marta

    2016-01-01

    Introduction The effect of nitric oxide (NO) on the human body is very important due its physiological regulation of the following functions of airways: modulation of ciliary movement and maintenance of sterility in sinuses. Aim To evaluate the diagnostic significance of NO concentrations in exhaled air from the upper and lower airways in patients diagnosed with allergic rhinitis (AR). Material and methods The subjects included in the study were a group of 30 people diagnosed with sensitivity to environmental allergens and a control group consisting of 30 healthy subjects. The measurement of NO in the air exhaled from the lower and upper airways was performed using an on-line method by means of Restricted Exhaled Breath (REB), as well as using the measurement procedure (chemiluminescence) set out in the guidelines prepared in 2005 by the American Thoracic Society and the European Respiratory Society. Results In the late phase of the allergic reaction, higher values of the level of exhaled NO concentration from the lower airways were observed in the groups of subjects up to the threshold values of 25.17 ppb in the group of subjects with year-round allergic rhinitis and 21.78 ppb in the group with diagnosed seasonal allergic rhinitis. The difference in the concentration of NO exhaled from the lungs between the test group and the control group in the 4th h of the test was statistically significant (p = 0.045). Conclusions Exhaled NO should be considered as a marker of airway inflammation. It plays an important role in the differential diagnosis of allergy. PMID:27279816

  7. The 17O Excess of Stratospheric Nitrous Oxide in Mid-latitude Air

    NASA Astrophysics Data System (ADS)

    Ridley, A.; Kaiser, J.; Laube, J. C.

    2015-12-01

    Tropospheric nitrous oxide (N2O) has a 17O excess of (0.9±0.1) ‰ relative to Vienna Standard Mean Ocean Water (VSMOW). The origin of this 17O excess is under debate: tropospheric and stratospheric in-situ sources as well as isotope fractionation and isotope exchange during biological N2O production are all considered to make a contribution, as might the stratospheric photolysis sink. To constrain the relative contributions of the different processes and to improve our understanding of the underlying atmospheric chemical and microbial processes, more measurements are required. We have measured the 17O excess of stratospheric samples from mid-latitudes, from altitudes between 8 and 26 km. N2O was extracted cryogenically, separated from CO2 and CHF3 by a PoraPlotQ pre-column and then thermally decomposed in a gold furnace at 900 ºC. The precision for the 17O excess of a single 5 nmol N2O aliquot was ±0.3 ‰. This dataset significantly enhances the limited range of oxygen triple isotope measurements in mostly lower stratospheric samples reported by Cliff et al. (1999). The average 17O excess of the stratospheric samples analysed was (-0.19 ±0.46) ‰ relative to tropospheric N2O. Since the 17O excess of the first measurements of stratospheric air is not significantly different to that in tropospheric air, this data suggests that the 17O excess is not of stratospheric origin. This confirms the idea that the origin of the 17O excess is not due to either stratospheric photolysis or reaction with electronically excited oxygen atoms. It suggests that the origin of the 17O excess may therefore be related to tropospheric in situ sources, e.g. NH2+NO2 as proposed by Röckmann et al., 2001, or to microbial nitrogen conversion reactions as suggested by Kaiser and Röckmann, 2005.

  8. Thermodynamic and kinetic study of phenol degradation by a non-catalytic wet air oxidation process.

    PubMed

    Lefèvre, Sébastien; Boutin, Olivier; Ferrasse, Jean-Henry; Malleret, Laure; Faucherand, Rémy; Viand, Alain

    2011-08-01

    This work is dedicated to an accurate evaluation of thermodynamic and kinetics aspects of phenol degradation using wet air oxidation process. Phenol is a well known polluting molecule and therefore it is important having data of its behaviour during this process. A view cell is used for the experimental study, with an internal volume of 150 mL, able to reach pressures up to 30 MPa and temperatures up to 350°C. Concerning the thermodynamic phase equilibria, experimental and modelling results are obtained for different binary systems (water/nitrogen, water/air) and ternary system (water/nitrogen/phenol). The best model is the Predictive Soave Redlich Kwong one. This information is necessary to predict the composition of the gas phase during the process. It is also important for an implementation in a process simulation. The second part is dedicated to kinetics evaluation of the degradation of phenol. Different compounds have been detected using GC coupled with a MS. A kinetic scheme is deduced, taking into account the evolution of phenol, hydroquinones, catechol, resorcinol and acetic acid. The kinetic parameters are calculated for this scheme. These data are important to evaluate the evolution of the concentration of the different polluting molecules during the process. A simplified kinetic scheme, which can be easily implemented in a process simulation, is also determined for the direct degradation of phenol into H(2)O and CO(2). The Arrhenius law data obtained for the phenol disappearance are the following: k=1.8×10(6)±3.9×10(5)M(-1)s(-1) (pre-exponential factor) and E(a)=77±8 kJ mol(-1) (activation energy). PMID:21700312

  9. Temperature-modulated graphene oxide resistive humidity sensor for indoor air quality monitoring

    NASA Astrophysics Data System (ADS)

    de Luca, A.; Santra, S.; Ghosh, R.; Ali, S. Z.; Gardner, J. W.; Guha, P. K.; Udrea, F.

    2016-02-01

    In this paper we present a temperature-modulated graphene oxide (GO) resistive humidity sensor that employs complementary-metal-oxide-semiconductor (CMOS) micro-electro-mechanical-system (MEMS) micro-hotplate technology for the monitoring and control of indoor air quality (IAQ). GO powder is obtained by chemical exfoliation, dispersed in water and deposited via ink-jet printing onto a low power micro-hotplate. Atomic force microscopy (AFM) and transmission electron microscopy (TEM) show the typical layered and wrinkled morphology of the GO. Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and Fourier transform infra-red (FTIR) spectroscopy indicate that the GO flakes possess a significant number of oxygen containing functional groups (epoxy, carbonyl, hydroxyl) extremely attractive for humidity detection. Electro-thermal characterisation of the micro-hotplates shows a thermal efficiency of 0.11 mW per °C, resulting in a sensor DC power consumption of only 2.75 mW at 50 °C. When operated in an isothermal mode, the sensor response is detrimentally affected by significant drift, hysteretic behaviour, slow response/recovery times and hence poor RH level discrimination. Conversely, a temperature modulation technique coupled with a differential readout methodology results in a significant reduction of the sensor drift, improved linear response with a sensitivity of 0.14 mV per %, resolution below 5%, and a maximum hysteresis of +/-5% response and recovery times equal to 189 +/- 49 s and 89 +/- 5 s, respectively. These performance parameters satisfy current IAQ monitoring requirements. We have thus demonstrated the effectiveness of integrating GO on a micro-hotplate CMOS-compatible platform enabling temperature modulation schemes to be easily applied in order to achieve compact, low power, low cost humidity IAQ monitoring.In this paper we present a temperature-modulated graphene oxide (GO) resistive humidity sensor that employs complementary-metal-oxide

  10. Temperature-modulated graphene oxide resistive humidity sensor for indoor air quality monitoring.

    PubMed

    De Luca, A; Santra, S; Ghosh, R; Ali, S Z; Gardner, J W; Guha, P K; Udrea, F

    2016-02-28

    In this paper we present a temperature-modulated graphene oxide (GO) resistive humidity sensor that employs complementary-metal-oxide-semiconductor (CMOS) micro-electro-mechanical-system (MEMS) micro-hotplate technology for the monitoring and control of indoor air quality (IAQ). GO powder is obtained by chemical exfoliation, dispersed in water and deposited via ink-jet printing onto a low power micro-hotplate. Atomic force microscopy (AFM) and transmission electron microscopy (TEM) show the typical layered and wrinkled morphology of the GO. Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and Fourier transform infra-red (FTIR) spectroscopy indicate that the GO flakes possess a significant number of oxygen containing functional groups (epoxy, carbonyl, hydroxyl) extremely attractive for humidity detection. Electro-thermal characterisation of the micro-hotplates shows a thermal efficiency of 0.11 mW per °C, resulting in a sensor DC power consumption of only 2.75 mW at 50 °C. When operated in an isothermal mode, the sensor response is detrimentally affected by significant drift, hysteretic behaviour, slow response/recovery times and hence poor RH level discrimination. Conversely, a temperature modulation technique coupled with a differential readout methodology results in a significant reduction of the sensor drift, improved linear response with a sensitivity of 0.14 mV per %, resolution below 5%, and a maximum hysteresis of ±5%; response and recovery times equal to 189 ± 49 s and 89 ± 5 s, respectively. These performance parameters satisfy current IAQ monitoring requirements. We have thus demonstrated the effectiveness of integrating GO on a micro-hotplate CMOS-compatible platform enabling temperature modulation schemes to be easily applied in order to achieve compact, low power, low cost humidity IAQ monitoring. PMID:26842731

  11. Nitric Oxide and Oxygen Air-Contamination Effects on Extinction Limits of Non-Premixed Hydrocarbon-Air Flames for a HIFiRE Scramjet

    NASA Technical Reports Server (NTRS)

    Pellett, Gerald L.; Dawson, Lucy C.; Vaden, Sarah N.; Wilson, Lloyd G.

    2009-01-01

    Unique nitric oxide (NO) and oxygen air-contamination effects on the extinction Flame Strength (FS) of non-premixed hydrocarbon (HC) vs. air flames are characterized for 7 gaseous HCs, using a new idealized 9.3 mm straight-tube Opposed Jet Burner (OJB) at 1 atm. FS represents a laminar strain-induced extinction limit based on cross-section-average air jet velocity, Uair, that sustains combustion of a counter jet of gaseous fuel just before extinction. Besides ethane, propane, butane, and propylene, the HCs include ethylene, methane, and a 64 mole-% ethylene / 36 % methane mixture, the writer s previously recommended gaseous surrogate fuel for HIFiRE scramjet tests. The HC vs. clean air part of the work is an extension of a May 2008 JANNAF paper that characterized surrogates for the HIFiRE project that should mimic the flameholding of reformed (thermally- or catalytically-cracked) endothermic JP-like fuels. The new FS data for 7 HCs vs. clean air are thus consolidated with the previously validated data, normalized to absolute (local) axial-input strain rates, and co-plotted on a dual kinetically dominated reactivity scale. Excellent agreement with the prior data is obtained for all 7 fuels. Detailed comparisons are also made with recently published (Univ. Va) numerical results for ethylene extinction. A 2009-revised ethylene kinetic model (Univ. Southern Cal) led to predicted limits within approx. 5 % (compared to 45 %, earlier) of this writer s 2008 (and present) ethylene FSs, and also with recent independent data (Univ. Va) obtained on a new OJB system. These +/- 5 % agreements, and a hoped-for "near-identically-performing" reduced kinetics model, would greatly enhance the capability for accurate numerical simulations of surrogate HC flameholding in scramjets. The measured air-contamination effects on normalized FS extinction limits are projected to assess ongoing Arc-Heater-induced "facility test effects" of NO production (e.g., 3 mole-%) and resultant oxygen

  12. Oxidation kinetics of Haynes 230 alloy in air at temperatures between 650 and 850 °C

    NASA Astrophysics Data System (ADS)

    Jian, Li; Jian, Pu; Bing, Hua; Xie, Guangyuan

    Haynes 230 alloy was oxidized in air at temperatures between 650 and 850 °C. Thermogravimetry was used to measure the kinetics of oxidation. The formed oxides were identified by the thin film (small angle) X-ray diffraction technique. Cr 2O 3 and MnCr 2O 4 were found in the oxide scale. Multi-stage oxidation kinetics was observed, and each stage follows Wagner's parabolic law. The first slow oxidation stage corresponded to the growth of an Cr 2O 3 layer, controlled by Cr ions diffusion through the dense Cr 2O 3 scale. The faster second stage was a result of rapid diffusion of Mn ions passing through the established Cr 2O 3 scale to form MnCr 2O 4 on top of the Cr 2O 3 layer. A duplex oxide scale is expected. The third stage, with a rate close to that of the first stage, only appeared for oxidation in the intermediate temperature range, i.e., 750-800 °C, which can be explained by the interruption of the Mn flux that forms MnCr 2O 4.

  13. Air Quality Criteria for Ozone and Related Photochemical Oxidants (2006 Final)

    EPA Science Inventory

    Tropospheric or surface-level ozone (O3) is one of six major air pollutants regulated by National Ambient Air Quality Standards (NAAQS) under the U.S. Clean Air Act. As mandated by the Clean Air Act, the U.S. Environmental Protection Agency (EPA) must periodically review t...

  14. AIR QUALITY CRITERIA FOR OZONE AND RELATED PHOTOCHEMICAL OXIDANTS (External Review Draft, 1995)

    EPA Science Inventory

    The U.S. Environmental Protection Agency (EPA) promulgates the National Ambient Air Quality Standards (NAAQS) on the basis of scientific information contained in air quality criteria issued under Section 108 of the Clean Air Act. The previous ozone (03) criteria document, Air Qua...

  15. Acute effects of motor vehicle traffic-related air pollution exposures on measures of oxidative stress in human airways

    PubMed Central

    Laumbach, Robert J.; Kipen, Howard M.

    2014-01-01

    Epidemiological studies have linked exposure to traffic-related air pollutants to increased respiratory and cardiovascular morbidity and mortality. Evidence from human, animal, and in vitro studies supports an important role for oxidative stress in the pathophysiological pathways underlying the adverse health effects of air pollutants. In controlled-exposure studies of animals and humans, emissions from diesel engines, a major source of traffic-related air pollutants, cause pulmonary and systemic inflammation that is mediated by redox-sensitive signaling pathways. Assessment of human responses to traffic-related air pollution under realistic conditions is challenging due to the complex, dynamic nature of near-roadway exposure. Noninvasive measurement of biomarkers in breath and breath condensate may be particularly useful for evaluating the role of oxidative stress in acute responses to exposures that occur in vehicles or during near-roadway activities. Promising biomarkers include nitric oxide in exhaled breath, and nitrite/nitrate, malondialdehyde, and F2-isoprostanes in exhaled breath condensate. PMID:20716291

  16. Effects of Post-Pyrolysis Air Oxidation of Biomass Chars on Adsorption of Neutral and Ionizable Compounds.

    PubMed

    Xiao, Feng; Pignatello, Joseph J

    2016-06-21

    This study was conducted to understand the effects of thermal air oxidation of biomass chars experienced during formation or production on their adsorptive properties toward various compounds, including five neutral nonpolar and polar compounds and seven weak acids and bases (pKa = 3-5.2) selected from among industrial chemicals and the triazine and phenoxyacetic acid herbicide classes. Post-pyrolysis air oxidation (PPAO) at 400 °C of anoxically prepared wood and pecan shell chars for up to 40 min enhanced the mass-normalized adsorption at pH ∼ 7.4 of all test compounds, especially the weak acids and bases, by up to 100-fold. Both general and specific effects were identified. The general effect results from "reaming" of pores by the oxidative removal of pore wall matter and/or tarry deposits generated during the pyrolysis step. Reaming creates new surface area and enlarges nanopores, which helps relieve steric hindrance to adsorption. The specific effect results from creation of new acidic functionality that provides sites for the formation of very strong, charge-assisted hydrogen bonds (CAHB) with solutes having comparable pKa. The CAHB hypothesis was supported by competition experiments and the finding that weak acid anion adsorption increased with surface carboxyl content, despite electrostatic repulsion from the growing negative charge. The results provide insight into the effects of air oxidation on pollutant retention. PMID:27152745

  17. Short-Term Oxidation Studies on Nicrofer- 6025HT in Air at Elevated Temperatures for Advanced Coal Based Power Plants

    SciTech Connect

    Joshi, Vineet V.; Meier, Alan; Darsell, Jens T.; Nachimuthu, Ponnusamy; Bowden, Mark E.; Weil, K. Scott

    2013-04-01

    Several advanced air separation unit (ASU) designs being considered for use in coal gasification rely on the use of solid state mixed ionic and electronic conductors. Nicrofer-6025HT, a nickel-based alloy, has been identified as a potential manifold material to transport the hot gases into the ASUs. In the current study, isothermal oxidation tests were conducted on Nicrofer-6025HT in the temperature range of 700–900 °C for up to 24 h. The evolution of oxide scale was evaluated using SEM, XRD, and XPS. The composite surface oxide layer that formed consisted of an outer chromia-rich scale and an inner alumina scale. For the longer times at the higher temperatures evaluated, a NiCr2O4 spinel phase was located at the interface between the alumina and chromia. Based on the experimental results a four-step oxidation model was proposed.

  18. Air oxidation and seawater corrosion of Hastelloy S and Hastelloy C-4

    SciTech Connect

    Fullam, H.T.

    1980-03-01

    A program is currently under way at the Pacific Northwest Laboratory (PNL) to develop the data and technology needed to permit the licensing of /sup 90/SrF/sub 2/ as a radioisotope heat source fuel for terrestrial applications. The WESF /sup 90/SrF/sub 2/ storage capsule consists of a Hastelloy C-276 inner capsule (2 in. I.D. x 19 in. long) and a 316L stainless steel outer capsule (2-3/8 in. I.D. x 20 in. long). Preliminary experimental tests and theoretical calculations show that the WESF storage capsule is incapable of meeting current licensing requirements for heat sources that are to be used for terrestrial applications. Therefore, the DOE decision was to develop a new heat source design that would retain the existing WESF Hastelloy C-276 inner capsule and replace the current WESF outer capsule with a new outer capsule capable of meeting current licensing requirements. Based on a number of factors, Hastelloy S was selected as the outer capsule material. Hastelloy C-4 was selected as a backup material in case the Hastelloy S had to be rejected for any reason. This report summarizes the results of studies carried out to determine the effects of both air oxidation at heat source operating temperatures and seawater corrosion on the tensile properties of the outer capsule materials.

  19. Nitric Oxide PLIF Visualization of Simulated Fuel-Air Mixing in a Dual-Mode Scramjet

    NASA Technical Reports Server (NTRS)

    Cantu, Luca M. L.; Gallo, Emanuela C. A.; Cutler, Andrew D.; Bathel, Brett F.; Danehy, Paul M.; Rockwell, Robert D.; Goyne, Christopher P.; McDaniel, James C.

    2015-01-01

    Nitric oxide (NO) planar induced laser fluorescence (PLIF) measurements have been performed in a small scale scramjet combustor at the University of Virginia Aerospace Research Laboratory at nominal simulated Mach 5 flight. A mixture of NO and N2 was injected at the upstream end of the inlet isolator as a surrogate for ethylene fuel, and the mixing of this fuel simulant was studied with and without a shock train. The shock train was produced by an air throttle, which simulated the blockage effects of combustion downstream of the cavity flame holder. NO PLIF signal was imaged in a plane orthogonal to the freestream at the leading edge of the cavity. Instantaneous planar images were recorded and analyzed to identify the most uniform cases, which were achieved by varying the location of the fuel injection and shock train. This method was used to screen different possible fueling configurations to provide optimized test conditions for follow-on combustion measurements using ethylene fuel. A theoretical study of the selected NO rotational transitions was performed to obtain a LIF signal that is linear with NO mole fraction and approximately independent of pressure and temperature.

  20. Layered perovskite oxide: a reversible air electrode for oxygen evolution/reduction in rechargeable metal-air batteries.

    PubMed

    Takeguchi, Tatsuya; Yamanaka, Toshiro; Takahashi, Hiroki; Watanabe, Hiroshi; Kuroki, Tomohiro; Nakanishi, Haruyuki; Orikasa, Yuki; Uchimoto, Yoshiharu; Takano, Hiroshi; Ohguri, Nobuaki; Matsuda, Motofumi; Murota, Tadatoshi; Uosaki, Kohei; Ueda, Wataru

    2013-07-31

    For the development of a rechargeable metal-air battery, which is expected to become one of the most widely used batteries in the future, slow kinetics of discharging and charging reactions at the air electrode, i.e., oxygen reduction reaction (ORR) and oxygen evolution reaction (OER), respectively, are the most critical problems. Here we report that Ruddlesden-Popper-type layered perovskite, RP-LaSr3Fe3O10 (n = 3), functions as a reversible air electrode catalyst for both ORR and OER at an equilibrium potential of 1.23 V with almost no overpotentials. The function of RP-LaSr3Fe3O10 as an ORR catalyst was confirmed by using an alkaline fuel cell composed of Pd/LaSr3Fe3O10-2x(OH)2x·H2O/RP-LaSr3Fe3O10 as an open circuit voltage (OCV) of 1.23 V was obtained. RP-LaSr3Fe3O10 also catalyzed OER at an equilibrium potential of 1.23 V with almost no overpotentials. Reversible ORR and OER are achieved because of the easily removable oxygen present in RP-LaSr3Fe3O10. Thus, RP-LaSr3Fe3O10 minimizes efficiency losses caused by reactions during charging and discharging at the air electrode and can be considered to be the ORR/OER electrocatalyst for rechargeable metal-air batteries. PMID:23802735

  1. FY-09 Report: Experimental Validation of Stratified Flow Phenomena, Graphite Oxidation, and Mitigation Strategies of Air Ingress Accidents

    SciTech Connect

    Chang H. Oh; Eung S. Kim

    2009-12-01

    The Idaho National Laboratory (INL), under the auspices of the U.S. Department of Energy, is performing research and development that focuses on key phenomena important during potential scenarios that may occur in the Next Generation Nuclear Plant (NGNP)/Gen-IV very high temperature reactor (VHTR). Phenomena Identification and Ranking Studies to date have identified that an air ingress event following on the heels of a VHTR depressurization is a very important incident. Consequently, the development of advanced air ingress-related models and verification and validation data are a very high priority for the NGNP Project. Following a loss of coolant and system depressurization incident, air will enter the core through the break, leading to oxidation of the in-core graphite structure and fuel. If this accident occurs, the oxidation will accelerate heat-up of the bottom reflector and the reactor core and will eventually cause the release of fission products. The potential collapse of the core bottom structures causing the release of CO and fission products is one of the concerns. Therefore, experimental validation with the analytical model and computational fluid dynamic (CFD) model developed in this study is very important. Estimating the proper safety margin will require experimental data and tools, including accurate multidimensional thermal-hydraulic and reactor physics models, a burn-off model, and a fracture model. It will also require effective strategies to mitigate the effects of oxidation. The results from this research will provide crucial inputs to the INL NGNP/VHTR Methods Research and Development project. The second year of this three-year project (FY-08 to FY-10) was focused on (a) the analytical, CFD, and experimental study of air ingress caused by density-driven, stratified, countercurrent flow; (b) advanced graphite oxidation experiments and modeling; (c) experimental study of burn-off in the core bottom structures, (d) implementation of advanced

  2. Kaolinite-catalyzed air oxidation of hydrazine: Consideration of several compositional, structural and energetic factors in surface activation

    NASA Technical Reports Server (NTRS)

    Coyne, L. M.; Mariner, R.; Rice, A.

    1991-01-01

    Clay minerals have been shown to have numerous, curious, energetic properties by virtue of ultra-violet light release which can be triggered by gentle environmental changes such as wetting and dewetting by a variety of liquids, unique among them water and hydrazine. Since both water and hydrazine play multiple key roles in the air-oxidation of hydrazine on kaolinite surfaces, this reaction would seem to have prime potential for studying interrelationships of energy storage, release and chemical reactivity of clay surfaces, capacities basic to either the Bernal or Cairns-Smith roles of minerals in the origin of life. Establishment of the capacity for stored electronic energy to significantly alter surface chemistry is important, regardless of the reaction chosen to demonstrate it. Hydrazine air oxidation is overawingly complex, given the possibilities for step-wise control and monitoring of parameters. In the light of recently extended characterization of the kaolinite and model sheet catalysts we used to study hydrazine oxidation and gamma-irradiated silica, previous studies of hydrazine air-oxidation on aluminosilicate surfaces have been reevaluated. Our former conclusion remains intact that, whereas trace structural and surface contaminants do play some role in the catalysis of oxidation, they are not the only, nor even the dominant, catalytic centers. Initial intermediates in the oxidation can now be proposed which are consistent with production via O(-)-centers as well as ferric iron centers. The greater than square dependence of the initial reaction rate on the weight of the clay is discussed in the light of these various mechanistic possibilities.

  3. Effects of Wet Air and Synthetic Combustion Gas Atmospheres on the Oxidation Behavior of Mo-Si-B Alloys

    SciTech Connect

    Kramer, M.J.; Thom, A.J.; Mandal, P.; Behrani, V.; Akinc, M.

    2003-04-24

    Continuing our work on understanding the oxidation behavior of multiphase composite alloys based on the Mo-Si-B system, we investigated three alloys in the Mo-Si-B system, designated as A1, A2, and A3. The nominal phase assemblages of these alloys are: A1 = Mo{sub 5}Si{sub 3}B{sub x} (T1)-MoSi{sub 2}-MoB, A2 = T1-Mo{sub 5}SiB{sub 2} (T2)-Mo{sub 3}Si, and A3 = Mo-T2-Mo{sub 3}Si. Our previous work showed that for exposures to 1100 C, all alloys formed a protective oxide scale in dry air. Exposures to wet air containing about 150 Torr water promoted the formation of a multiphase layer near the scale/alloy interface composed of Mo and MoO{sub 2}. Interrupted mass loss measurements indicated a near zero mass change. In the present study, isothermal mass measurements were conducted in order to quantitatively determine the oxidation rate constants at 1000 C in both dry and wet air. These measurements are critical for understanding the nature of scale development during the initial exposure, as well as the nature of scale stability during the long-term exposure. Isothermal measurements were also conducted at 1600 C in dry air to make an initial determination of alloy stability with respect to Vision 21 goals. We also conducted alloy oxidation testing in a synthetic oxidizing combustion atmosphere. Alloys were exposed up to 300 hours at 1100 C to a gas mixture having an approximate gas composition of N{sub 2} - 13 CO{sub 2} - 10 H{sub 2}O - 4 O{sub 2}. This gas composition simulates oxidizing flue gas, but does not contain a sulfidizing agent that would also be present in flue gas. The oxidized samples were carefully analyzed by SEM/EDS. This analysis will be discussed to provide an understanding of the role of water vapor and the synthetic combustion atmosphere on the oxidative stability of Mo-Si-B alloys.

  4. Oxidation Behavior of a Pd43Cu27Ni10P20 Bulk Metallic Glass and Foam in Dry Air

    NASA Astrophysics Data System (ADS)

    Kai, W.; Ren, I. F.; Barnard, B.; Liaw, P. K.; Demetriou, M. D.; Johnson, W. L.

    2010-07-01

    The oxidation behavior of both Pd43Cu27Ni10P20 bulk metallic glass (Pd4-BMG) and its amorphous foam containing 45 pct porosity (Pd4-AF) was investigated over the temperature range of 343 K (70 °C) to 623 K (350 °C) in dry air. The results showed that virtually no oxidation occurred in the Pd4-BMG at T < 523 K (250 °C), revealing the alloy’s favorable oxidation resistance in this temperature range. In addition, the oxidation kinetics at T ≥ 523 K (250 °C) followed a parabolic-rate law, and the parabolic-rate constants ( k p values) generally increased with temperature. It was found that the oxidation k p values of the Pd4-AF are slightly lower than those of the Pd4-BMG, indicating that the porous structure contributes to improving the overall oxidation resistance. The scale formed on the alloys was composed exclusively of CuO at T ≥ 548 K (275 °C), whose thickness gradually increased with increasing temperature. In addition, the amorphous structure remained unchanged at T ≤ 548 K (275 °C), while a triplex-phase structure developed after the oxidation at higher temperatures, consisting of Pd2Ni2P, Cu3P, and Pd3P.

  5. ESR investigation of the oxidative damage in lungs caused by asbestos and air pollution particles

    NASA Astrophysics Data System (ADS)

    Kadiiska, M. B.; Ghio, A. J.; Mason, R. P.

    2004-05-01

    Exposure to asbestos and air pollution particles can be associated with increased human morbidity and mortality. However, the molecular mechanism of lung injuries remains unknown. It has been postulated that the in vivo toxicity results from the catalysis of free radical generation. Using electron spin resonance (ESR) in conjunction with the spin trap α-(4-pyridyl-1-oxide)- N- tert-butylnitrone (4-POBN) we previously investigated in vivo free radical production by rats treated with intratracheal instillation of asbestos (crocidolite fibers) and an emission source air pollution particle (oil fly ash). In this report we compare the effect of two different exposures on the type of free radicals they induce in in vivo animal model. Twenty-four hours after the exposure, ESR spectroscopy of the chloroform extract from lungs of animals exposed to either asbestos or oil fly ash gave a spectrum consistent with a carbon-centered radical adduct ( aN=15.01 G and aH=2.46 G). To test whether free radical formation occurred in vivo and not in vitro, a number of control experiments were performed. Combinations (both individually and together) of asbestos or oil fly ash and 4-POBN were added to lung homogenate of unexposed rats prior to chloroform extraction. No detectable ESR signal resulted. To exclude the possibility of ex vivo free radical generation, asbestos or oil fly ash was added to lung homogenate of an animal treated with 4-POBN. Also, 4-POBN was added to lung homogenate from rats instilled with asbestos or oil fly ash. Neither system produced radical adducts, indicating that the ESR signal detected in the lung extracts of the treated animals must be produced in vivo and not ex vivo or in vitro. In conclusion, ESR analysis of lung tissue demonstrated that both exposures produce lipid-derived radical metabolites despite their different composition and structure. Analogously, both exposures provide evidence of in vivo enhanced lipid peroxidation. Furthermore, it is

  6. Oxidation of orthorhombic titanium aluminide Tl-22AL-25NB in air between 650 and 1000 °C

    NASA Astrophysics Data System (ADS)

    Leyens, C.

    2001-04-01

    The oxidation behavior of orthorhombic titanium aluminide alloy Ti-22Al-25Nb was studied in air between 650 and 1000 °C by isothermal thermogravimetry and postoxidation scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and x-ray diffraction. Microhardness measurements were performed after exposure to gage hardening due to nitrogen and oxygen ingress. The parabolic rate constant of Ti-22Al-25Nb was of the same order as conventional titanium alloys and Ti3Al-based titanium aluminides at and below 750 °C. Between 800 and 1000 °C, the oxidation resistance of Ti-22Al-25Nb was as good as that of γ-TiAl based aluminides; however, the growth rate changed from parabolic to linear after several tens of hours at 900 and 1000 °C. The mixed oxide scale consisted of TiO2, AlNbO4, and Al2O3, with TiO2 being the dominant oxide phase. Underneath the oxide scale, a nitride-containing layer formed in the temperature range investigated, and at 1000 °C, internal oxidation was observed below this layer. In all cases, oxygen diffused deeply into the subsurface zone and caused severe embrittlement. Microhardness measurements revealed that Ti-22Al-25Nb was hardened in a zone as far as 300 µm below the oxide scale when exposed to air at 900 °C for 500 h. The peak hardness depended on exposure time and reached five times the average hardness of the bulk material under the above conditions.

  7. Exfoliation at the liquid/air interface to assemble reduced graphene oxide ultrathin films for a flexible noncontact sensing device.

    PubMed

    Wang, Xuewen; Xiong, Zuoping; Liu, Zheng; Zhang, Ting

    2015-02-25

    Reduced graphene oxide ultrathin films are fabricated by a reproducible exfoliation method at the liquid/air interface, and they show high transparency, tunable sheet resistance, uniform electric conductivity, and structural homogeneity over a large area. A flexible relative humidity sensing matrix is demonstrated and it is shown to be excellent for close proximity sensing without touching it. This method opens up a novel avenue for future human-machine interaction applications. PMID:25522328

  8. Integration of photocatalytic oxidation with air stripping of contaminated aquifers. Report for 1 October 1993--30 June 1997

    SciTech Connect

    Changrani, R.; Raupp, G.B.; Turchi, C.

    1998-12-01

    The global objective of this work was to evaluate the integration of gas-solid ultraviolet (UV) photocatalytic oxidation (PCO) downstream of an air stripper as a technology for cost-effectively treating water pumped from an aquifer contaminated with chlorinated volatile organic compounds (VOCs). Experimental work was performed at the bench-scale in the laboratory during the first phase of the project, and at the pilot-scale in a simulated field-test situation during the second phase.

  9. Carvedilol alleviates adjuvant-induced arthritis and subcutaneous air pouch edema: Modulation of oxidative stress and inflammatory mediators

    SciTech Connect

    Arab, Hany H.; El-Sawalhi, Maha M.

    2013-04-15

    Rheumatoid arthritis (RA) is a systemic inflammatory disease with cardiovascular complications as the leading cause of morbidity. Carvedilol is an adrenergic antagonist which has been safely used in treatment of several cardiovascular disorders. Given that carvedilol has powerful antioxidant/anti-inflammatory properties, we aimed to investigate its protective potential against arthritis that may add further benefits for its clinical usefulness especially in RA patients with concomitant cardiovascular disorders. Two models were studied in the same rat; adjuvant arthritis and subcutaneous air pouch edema. Carvedilol (10 mg/kg/day p.o. for 21 days) effectively suppressed inflammation in both models with comparable efficacy to the standard anti-inflammatory diclofenac (5 mg/kg/day p.o.). Notably, carvedilol inhibited paw edema and abrogated the leukocyte invasion to air pouch exudates. The latter observation was confirmed by the histopathological assessment of the pouch lining that revealed mitigation of immuno-inflammatory cell influx. Carvedilol reduced/normalized oxidative stress markers (lipid peroxides, nitric oxide and protein thiols) and lowered the release of inflammatory cytokines (TNF-α and IL-6), and eicosanoids (PGE{sub 2} and LTB{sub 4}) in sera and exudates of arthritic rats. Interestingly, carvedilol, per se, didn't present any effect on assessed biochemical parameters in normal rats. Together, the current study highlights evidences for the promising anti-arthritic effects of carvedilol that could be mediated through attenuation of leukocyte migration, alleviation of oxidative stress and suppression of proinflammatory cytokines and eicosanoids. - Highlights: ► Carvedilol possesses promising anti-arthritic properties. ► It markedly suppressed inflammation in adjuvant arthritis and air pouch edema. ► It abrogated the leukocyte invasion to air pouch exudates and linings. ► It reduced/normalized oxidative stress markers in sera and exudates of

  10. Analysis of effect of flameholder characteristics on lean, premixed, partially vaporized fuel-air mixtures quality and nitrogen oxides emissions

    NASA Technical Reports Server (NTRS)

    Cooper, L. P.

    1981-01-01

    An analysis was conducted of the effect of flameholding devices on the precombustion fuel-air characteristics and on oxides of nitrogen (NOx) emissions for combustion of premixed partially vaporized mixtures. The analysis includes the interrelationships of flameholder droplet collection efficiency, reatomization efficiency and blockage, and the initial droplet size distribution and accounts for the contribution of droplet combustion in partially vaporized mixtures to NOx emissions. Application of the analytical procedures is illustrated and parametric predictions of NOx emissions are presented.

  11. AIR QUALITY CRITERIA FOR OZONE AND RELATED PHOTOCHEMICAL OXIDANTS VOLUME I OF III (Final, 1996)

    EPA Science Inventory

    The U.S. Environmental Protection Agency (EPA) promulgates the National Ambient Air Quality Standards (NAAQS) on the basis of scientific information contained in air quality criteria documents. The previous ozone (O3) criteria document, Air Quality Criteria for Ozone and Other Ph...

  12. Characterization of predominantly hydrophobic poly(styrene)-poly(ethylene oxide) copolymers at air/water and cyclohexane/water interfaces

    SciTech Connect

    Gragson, D.E.; Jensen, J.M.; Baker, S.M.

    1999-09-14

    Interfacial tension measurements are employed to explore the spreading behavior of predominantly hydrophobic poly(styrene)--poly(ethylene oxide), PS-PEO, diblock copolymers at air/water and cyclohexane/water interfaces. Two copolymers with 7%- and 15.5%-PEO are examined in this study. The former is expected to have a PS block limiting area in air roughly equal to the limiting PEO pancake area, whereas the latter is expected to have a limiting PS block area in air approximately 3 times smaller than the limiting PEO pancake area. At the air/water interface, the 7%-PEO copolymer does not spread well, which is attributed to interference from the hydrophobic PS block. In contrast, the 7%-PEO copolymer spreads well at the cyclohexane/water interface, producing an isotherm with a terminating mean molecular area 3 times smaller than that obtained at the air/water interface. The 15.5%-PEO copolymer spreads well at both the air/water ad cyclohexane/water interfaces due to less interference from the smaller hydrophobic PS block. These observations are compared to compression isotherms, and the results are discussed in terms of the solvating nature of the adjacent cyclohexane phase for the PS block.

  13. Multi-generational oxidation model to simulate secondary organic aerosol in a 3-D air quality model

    NASA Astrophysics Data System (ADS)

    Jathar, S. H.; Cappa, C. D.; Wexler, A. S.; Seinfeld, J. H.; Kleeman, M. J.

    2015-08-01

    Multi-generational gas-phase oxidation of organic vapors can influence the abundance, composition and properties of secondary organic aerosol (SOA). Only recently have SOA models been developed that explicitly represent multi-generational SOA formation. In this work, we integrated the statistical oxidation model (SOM) into SAPRC-11 to simulate the multi-generational oxidation and gas/particle partitioning of SOA in the regional UCD/CIT (University of California, Davis/California Institute of Technology) air quality model. In the SOM, evolution of organic vapors by reaction with the hydroxyl radical is defined by (1) the number of oxygen atoms added per reaction, (2) the decrease in volatility upon addition of an oxygen atom and (3) the probability that a given reaction leads to fragmentation of the organic molecule. These SOM parameter values were fit to laboratory smog chamber data for each precursor/compound class. SOM was installed in the UCD/CIT model, which simulated air quality over 2-week periods in the South Coast Air Basin of California and the eastern United States. For the regions and episodes tested, the two-product SOA model and SOM produce similar SOA concentrations but a modestly different SOA chemical composition. Predictions of the oxygen-to-carbon ratio qualitatively agree with those measured globally using aerosol mass spectrometers. Overall, the implementation of the SOM in a 3-D model provides a comprehensive framework to simulate the atmospheric evolution of organic aerosol.

  14. Multi-generational oxidation model to simulate secondary organic aerosol in a 3-D air quality model

    NASA Astrophysics Data System (ADS)

    Jathar, S. H.; Cappa, C. D.; Wexler, A. S.; Seinfeld, J. H.; Kleeman, M. J.

    2015-02-01

    Multi-generational gas-phase oxidation of organic vapors can influence the abundance, composition and properties of secondary organic aerosol (SOA). Only recently have SOA models been developed that explicitly represent multi-generational SOA formation. In this work, we integrated the statistical oxidation model (SOM) into SAPRC-11 to simulate the multi-generational oxidation and gas/particle partitioning of SOA in the regional UCD/CIT air quality model. In SOM, evolution of organic vapors by reaction with the hydroxyl radical is defined by (1) the number of oxygen atoms added per reaction, (2) the decrease in volatility upon addition of an oxygen atom and (3) the probability that a given reaction leads to fragmentation of the organic molecule. These SOM parameter values were fit to laboratory "smog chamber" data for each precursor/compound class. The UCD/CIT model was used to simulate air quality over two-week periods in the South Coast Air Basin of California and the eastern United States. For the regions and episodes tested, the traditional two-product SOA model and SOM produce similar SOA concentrations but a modestly different SOA chemical composition. Predictions of the oxygen-to-carbon ratio qualitatively agree with those measured globally using aerosol mass spectrometers. Overall, the implementation of the SOM in a 3-D model provides a comprehensive framework to simulate the atmospheric evolution of OA.

  15. Air plasma-material interactions at the oxidized surface of the PM1000 nickel-chromium superalloy

    NASA Astrophysics Data System (ADS)

    Panerai, Francesco; Marschall, Jochen; Thömel, Jan; Vandendael, Isabelle; Hubin, Annick; Chazot, Olivier

    2014-10-01

    Nickel-based superalloys are promising options for the thermal protection systems of hypersonic re-entry vehicles operating under moderate aerothermal heating conditions. We present an experimental study on the interactions between PM1000, an oxide dispersion strengthened nickel-chromium superalloy, and air plasma at surface temperatures between 1000 and 1600 K and pressures of 1500, 7500 and 10,000 Pa. Pre-oxidized PM1000 specimens are tested in high-enthalpy reactive air plasma flows generated by the Plasmatron wind tunnel at the von Karman Institute for Fluid Dynamics. Microscopic analysis of plasma-exposed specimens shows enhanced damage to the chromia scale at the lowest plasma pressure. Elemental surface analysis reveals the loss of Cr and the enhancement of Ni at the scale surface. A thermodynamic analysis supports the accelerated volatilization of Cr2O3 and the relative stability of NiO in the presence of atomic oxygen. Changes in the reflectance and emissivity of the oxidized surfaces due to plasma-exposure are presented. The catalytic efficiencies for dissociated air species recombination are determined as a function of surface temperature and pressure through a numerical rebuilding procedure and are compared with values presented in the literature for the same material.

  16. Review of research results for the photocatalytic oxidation of hazardous wastes in air

    SciTech Connect

    Nimlos, M R; Wolfrum, E J; Gratson, D A; Watt, A S; Jacoby, W A; Turchi, C

    1995-01-01

    Laboratory experiments of gas-phase photocatalytic oxidation (PCO) at NREL have focused on measurements that can help commercialize this technology for treating gaseous air streams. This effort proceeds earlier NREL work and studies conducted elsewhere which demonstrated the general applicability of PCO. The more recent work has concentrated on: (1) the kinetics of the PCO process; (2) the formation and destruction of intermediates; and (3) possible enhancements to improve the destruction rates. The results from these studies will be used to help design large scale PCO equipment and they will be used to evaluate the economics of the PCO process. For trichloroethylene and ethanol, extensive studies of the rates of destruction have yielded kinetic parameters for the destruction of intermediates as well as the substrate. The kinetics of intermediates is essential for sizing a large scale reactor, as complete conversion to carbon dioxide is often desired. The kinetic data from these laboratory studies has been used for analyzing IT`s pilot PCO reactor and has been used to suggest modifications to this unit. For compounds that are more difficult to destroy (such as the components of BTEX), rate enhancement experiments have been conducted. These compounds represent a very large market for this technology and improvement of the rate of the process should make it competitive. Towards this goal, the enhancement of the destruction of BTEX components have been studied. Experiments have demonstrated that there is a significant increase in the rates of destruction of BTEX with the addition of ozone. Preliminary economic assessments have shown that PCO with ozone may be cost competitive. Future laboratory experiments of PCO will focus on refinements of what has been learned. Rate measurements will also be expanded to include other compounds representing significant markets for the PCO technology.

  17. Surface activation of air oxidation of hydrazine on kaolinite. 2. Consideration of oxidizing/reducing entities in relationship to other compositional, structural, and energetic factors

    NASA Technical Reports Server (NTRS)

    Coyne, L. M.; Summers, D. P.

    1991-01-01

    The rates (previously reported) for the air oxidation of hydrazine on kaolinite and substituent oxides of kaolinite showed a complex dependence on the relative amounts of several structural oxidizing/reducing entities within the reaction-promoting solids. The rates indicated an important role of the clay but no dominant role of any one of the oxidizing/reducing entities. In this paper we review (a) the reaction-promoting activity of these centers as studied in other systems, (b) various spectroscopic results showing interaction between these entities in clays, and (c) reported spectroscopic studies of the complexation between hydrazine and aluminosilicate surfaces as a whole, in an effort to propose a mechanism for the reaction. Whereas some uncertainties remain, the present synthesis concludes that a mechanism operating through single electron/hole transfers and hydrogen atom transfers by discrete centers is adequate to explain the observed rate behaviors including the observed second order dependence of the oxidation rate on catalyst amount. The effects of these operations on the catalyst can result in no alteration of, or complete or partial electronic relaxation of its contingent of trapped separated charge pairs. The degree to which surface complexation as a whole, intercalation, or luminescent processes may also be associated with the reaction cannot be adequately assessed with the information in hand.

  18. Investigation of low temperature solid oxide fuel cells for air-independent UUV applications

    NASA Astrophysics Data System (ADS)

    Moton, Jennie Mariko

    Unmanned underwater vehicles (UUVs) will benefit greatly from high energy density (> 500 Wh/L) power systems utilizing high-energy-density fuels and air-independent oxidizers. Current battery-based systems have limited energy densities (< 400 Wh/L), which motivate development of alternative power systems such as solid oxide fuel cells (SOFCs). SOFC-based power systems have the potential to achieve the required UUV energy densities, and the current study explores how SOFCs based on gadolinia-doped ceria (GDC) electrolytes with operating temperatures of 650°C and lower may operate in the unique environments of a promising UUV power plant. The plant would contain a H 2O2 decomposition reactor to supply humidified O2 to the SOFC cathode and exothermic aluminum/H2O combustor to provide heated humidified H2 fuel to the anode. To characterize low-temperature SOFC performance with these unique O2 and H2 source, SOFC button cells based on nickel/GDC (Gd0.1Ce0.9O 1.95) anodes, GDC electrolytes, and lanthanum strontium cobalt ferrite (La0.6Sr0.4Co0.2Fe0.8O3-δ or LSCF)/GDC cathodes were fabricated and tested for performance and stability with humidity on both the anode and the cathode. Cells were also tested with various reactant concentrations of H2 and O2 to simulate gas depletion down the channel of an SOFC stack. Results showed that anode performance depended primarily on fuel concentration and less on the concentration of the associated increase in product H2O. O 2 depletion with humidified cathode flows also caused significant loss in cell current density at a given voltage. With the humidified flows in either the anode or cathode, stability tests of the button cells at 650 °C showed stable voltage is maintained at low operating current (0.17 A/cm2) at up to 50 % by mole H2O, but at higher current densities (0.34 A/cm2), irreversible voltage degradation occurred at rates of 0.8-3.7 mV/hour depending on exposure time. From these button cell results, estimated average

  19. Detection of nitric oxide in exhaled air using cavity enhanced absorption spectroscopy

    NASA Astrophysics Data System (ADS)

    Medrzycki, R.; Wojtas, J.; Rutecka, B.; Bielecki, Z.

    2013-07-01

    The article describes an application one of the most sensitive optoelectronic method - Cavity Enhanced Absorption Spectroscopy in investigation of nitric oxide in exhaled breath. Measurement of nitric oxide concentration in exhaled breath is a quantitative, non-invasive, simple, and safe method of respiratory inflammation and asthma diagnosis. For detection of nitric oxide by developed optoelectronic sensor the vibronic molecular transitions were used. The wavelength ranges of these transitions are situated in the infrared spectral region. A setup consists of the optoelectronic nitric oxide sensor integrated with sampling and sample conditioning unit. The constructed detection system provides to measure nitric oxide in a sample of 0-97% relative humidity.

  20. OH-Radical Oxidation of Surface-Active cis-Pinonic Acid at the Air-Water Interface.

    PubMed

    Enami, Shinichi; Sakamoto, Yosuke

    2016-05-26

    Gaseous biogenic volatile organic compounds (BVOCs) are immediately oxidized by gaseous oxidants to form BVOC-acids that rapidly condense onto aqueous aerosol phase and thus contribute to the growth of atmospheric particles. Because BVOC-acids are highly hydrophobic and hence surface-active in nature, it seems critical to study the oxidation by gaseous hydroxyl radical (·OH(g)) at the air-water interface. Here we report on the fast (≤10 μs) oxidation of aqueous cis-pinonic acid (C10H16O3, CPA, cis-pinonate anion's m/z = 183), a representative BVOC-acid, by ·OH(g) at the air-water interface for the first time. We find that cis-pinonate anion is more enriched at the air-water interface by ∼4 and ∼14 times than n-octanoate anion at 10 and 100 μM, respectively, as revealed by an interface-specific mass spectrometry of the equimolar mixture of microjets. Exposure of aqueous CPA microjets to ·OH(g) pulses from the 266 nm laser photolysis of O3(g)/O2(g)/H2O(g)/N2(g) mixtures yields pinonic peroxyl radicals (m/z = 214) that lead to the functionalization products carbonyls (m/z = 197), alcohols (m/z = 199), and pinonic hydroperoxides (m/z = 215) in addition to smaller-mass products including carbonyls (m/z = 155 and 157). We confirmed the formation of the corresponding alcohols, aldehydes, and hydroperoxides in experiments performed in D2O solvent. The analysis of total mass balance implies a significant amount (>70%) of products would be emitted into the gas-phase during the heterogeneous ·OH-oxidations. Our results suggest ·OH-oxidations of amphiphilic BVOC-acids at the air-water interface may play a far more significant role in photochemical aging process of aqueous aerosols than previously assumed. PMID:27098046

  1. Mechanism of the Initial Oxidation of Hydrogen andHalogen Terminated Ge(111) Surfaces in Air

    SciTech Connect

    Sun, Shiyu; Sun, Yun; Liu, Zhi; Lee, Dong-Ick; Pianetta, Piero; /SLAC, SSRL

    2006-08-23

    The initial stage of the oxidation of Ge(111) surfaces etched by HF, HCl and HBr solutions is systematically studied using synchrotron radiation photoelectron spectroscopy (SR-PES). We perform controlled experiments to differentiate the effects of different oxidation factors. SR-PES results show that both moisture and oxygen contribute to the oxidation of the surfaces; however, they play different roles in the oxidation process. Moisture effectively replaces the hydrogen and halogen termination layers with hydroxyl (OH), but hardly oxidizes the surfaces further. On the other hand, dry oxygen does not replace the termination layers, but breaks the Ge-Ge back bonds and oxidizes the substrates with the aid of moisture. In addition, room light enhances the oxidation rate significantly.

  2. 75 FR 57463 - Review of the Secondary National Ambient Air Quality Standards for Oxides of Nitrogen and Oxides...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-09-21

    ....'' The air quality criteria are to ``accurately reflect the latest scientific knowledge useful in... advances in scientific knowledge on the effects of the pollutant on public health or welfare. The EPA is... Scientific Advisory Committee (CASAC) and to solicit public comment on the overall structure, framing of...

  3. Synthesis of air-stable, volatile uranium(IV) and (VI) compounds and their gas-phase conversion to uranium oxide films.

    PubMed

    Appel, Linus; Leduc, Jennifer; Webster, Christopher L; Ziller, Joseph W; Evans, William J; Mathur, Sanjay

    2015-02-01

    Four air-stable, volatile uranium heteroarylalkenolates have been synthesized and characterized by three synthetic approaches and their gas phase deposition to uranium oxide films has been examined. PMID:25537920

  4. Inflammatory and Oxidative Stress Responses of Healthy Young Adults to Changes in Air Quality during the Beijing Olympics

    PubMed Central

    Huang, Wei; Wang, Guangfa; Lu, Shou-En; Kipen, Howard; Wang, Yuedan; Hu, Min; Lin, Weiwei; Rich, David; Ohman-Strickland, Pamela; Diehl, Scott R.; Zhu, Ping; Tong, Jian; Gong, Jicheng; Zhu, Tong

    2012-01-01

    Rationale: Unprecedented pollution control actions during the Beijing Olympics provided a quasi-experimental opportunity to examine biologic responses to drastic changes in air pollution levels. Objectives: To determine whether changes in levels of biomarkers reflecting pulmonary inflammation and pulmonary and systemic oxidative stress were associated with changes in air pollution levels in healthy young adults. Methods: We measured fractional exhaled nitric oxide, a number of exhaled breath condensate markers (H+, nitrite, nitrate, and 8-isoprostane), and urinary 8-hydroxy-2-deoxyguanosine in 125 participants twice in each of the pre- (high pollution), during- (low pollution), and post-Olympic (high pollution) periods. We measured concentrations of air pollutants near where the participants lived and worked. We used mixed-effects models to estimate changes in biomarker levels across the three periods and to examine whether changes in biomarker levels were associated with changes in pollutant concentrations, adjusting for meteorologic parameters. Measurements and Main Results: From the pre- to the during-Olympic period, we observed significant and often large decreases (ranging from −4.5% to −72.5%) in levels of all the biomarkers. From the during-Olympic to the post-Olympic period, we observed significant and larger increases (48–360%) in levels of these same biomarkers. Moreover, increased pollutant concentrations were consistently associated with statistically significant increases in biomarker levels. Conclusions: These findings support the important role of oxidative stress and that of pulmonary inflammation in mediating air pollution health effects. The findings demonstrate the utility of novel and noninvasive biomarkers in the general population consisting largely of healthy individuals. PMID:22936356

  5. Stabilized three-stage oxidation of DME/air mixture in a micro flow reactor with a controlled temperature profile

    SciTech Connect

    Oshibe, Hiroshi; Nakamura, Hisashi; Tezuka, Takuya; Hasegawa, Susumu; Maruta, Kaoru

    2010-08-15

    Ignition and combustion characteristics of a stoichiometric dimethyl ether (DME)/air mixture in a micro flow reactor with a controlled temperature profile which was smoothly ramped from room temperature to ignition temperature were investigated. Special attention was paid to the multi-stage oxidation in low temperature condition. Normal stable flames in a mixture flow in the high velocity region, and non-stationary pulsating flames and/or repetitive extinction and ignition (FREI) in the medium velocity region were experimentally confirmed as expected from our previous study on a methane/air mixture. In addition, stable double weak flames were observed in the low velocity region for the present DME/air mixture case. It is the first observation of stable double flames by the present methodology. Gas sampling was conducted to obtain major species distributions in the flow reactor. The results indicated that existence of low-temperature oxidation was conjectured by the production of CH{sub 2}O occured in the upstream side of the experimental first luminous flame, while no chemiluminescence from it was seen. One-dimensional computation with detailed chemistry and transport was conducted. At low mixture velocities, three-stage oxidation was confirmed from profiles of the heat release rate and major chemical species, which was broadly in agreement with the experimental results. Since the present micro flow reactor with a controlled temperature profile successfully presented the multi-stage oxidations as spatially separated flames, it is shown that this flow reactor can be utilized as a methodology to separate sets of reactions, even for other practical fuels, at different temperature. (author)

  6. 75 FR 70258 - Review of the Secondary National Ambient Air Quality Standards for Oxides of Nitrogen and Oxides...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-11-17

    ... Nitrogen and Oxides of Sulfur: Second External Review Draft (75 FR 57463, September 21, 2010). The EPA... a later date (75 FR 61486, October 5, 2010). The supplementary materials were: an errata sheet for... an atmospheric chemistry perspective as well as from an environmental effects perspective,...

  7. A perovskite oxide with high conductivities in both air and reducing atmosphere for use as electrode for solid oxide fuel cells.

    PubMed

    Lan, Rong; Cowin, Peter I; Sengodan, Sivaprakash; Tao, Shanwen

    2016-01-01

    Electrode materials which exhibit high conductivities in both oxidising and reducing atmospheres are in high demand for solid oxide fuel cells (SOFCs) and solid oxide electrolytic cells (SOECs). In this paper, we investigated Cu-doped SrFe0.9Nb0.1O3-δ finding that the primitive perovskite oxide SrFe0.8Cu0.1Nb0.1O3-δ (SFCN) exhibits a conductivity of 63 Scm(-1)and 60 Scm(-1) at 415 °C in air and 5%H2/Ar respectively. It is believed that the high conductivity in 5%H2/Ar is related to the exsolved Fe (or FeCu alloy) on exposure to a reducing atmosphere. To the best of our knowledge, the conductivity of SrFe0.8Cu0.1Nb0.1O3-δ in a reducing atmosphere is the highest of all reported oxides which also exhibit a high conductivity in air. Fuel cell performance using SrFe0.8Cu0.1Nb0.1O3-δ as the anode, (Y2O3)0.08(ZrO2)0.92 as the electrolyte and La0.8Sr0.2FeO3-δ as the cathode achieved a power density of 423 mWcm(-2) at 700 °C indicating that SFCN is a promising anode for SOFCs. PMID:27545200

  8. A perovskite oxide with high conductivities in both air and reducing atmosphere for use as electrode for solid oxide fuel cells

    PubMed Central

    Lan, Rong; Cowin, Peter I.; Sengodan, Sivaprakash; Tao, Shanwen

    2016-01-01

    Electrode materials which exhibit high conductivities in both oxidising and reducing atmospheres are in high demand for solid oxide fuel cells (SOFCs) and solid oxide electrolytic cells (SOECs). In this paper, we investigated Cu-doped SrFe0.9Nb0.1O3−δ finding that the primitive perovskite oxide SrFe0.8Cu0.1Nb0.1O3−δ (SFCN) exhibits a conductivity of 63 Scm−1and 60 Scm−1 at 415 °C in air and 5%H2/Ar respectively. It is believed that the high conductivity in 5%H2/Ar is related to the exsolved Fe (or FeCu alloy) on exposure to a reducing atmosphere. To the best of our knowledge, the conductivity of SrFe0.8Cu0.1Nb0.1O3−δ in a reducing atmosphere is the highest of all reported oxides which also exhibit a high conductivity in air. Fuel cell performance using SrFe0.8Cu0.1Nb0.1O3−δ as the anode, (Y2O3)0.08(ZrO2)0.92 as the electrolyte and La0.8Sr0.2FeO3−δ as the cathode achieved a power density of 423 mWcm−2 at 700 °C indicating that SFCN is a promising anode for SOFCs. PMID:27545200

  9. Trends of nitrogen oxides in ambient air in nine European cities between 1999 and 2010

    NASA Astrophysics Data System (ADS)

    Henschel, Susann; Le Tertre, Alain; Atkinson, Richard W.; Querol, Xavier; Pandolfi, Marco; Zeka, Ariana; Haluza, Daniela; Analitis, Antonis; Katsouyanni, Klea; Bouland, Catherine; Pascal, Mathilde; Medina, Sylvia; Goodman, Patrick G.

    2015-09-01

    Legislation controlling vehicle emissions has been credited with a general downward trend in NOx (NO2+NO) concentrations in Europe since the 1990's. However, recent studies suggest that traffic (roadside) (TR) NO2 concentrations have not decreased as expected, and in some cases increased, most likely due to the use of oxidation catalysts and particle filters in diesel vehicles (EURO III, IV, V, VI). In this study we describe the time trends in NOx, NO2 and NO concentrations in 9 European cities comparing TR and urban background (UB) monitoring locations. In each city, we collected hourly city-specific NOx, NO, and NO2 data from one TR and one UB monitoring site for each year. We describe hourly, weekly, seasonal and inter-annual patterns for periods corresponding to the implementation dates of various EURO vehicle emission standards regulating NOx emissions. The diurnal patterns in all 9 cities strongly reflected morning and evening traffic. In addition, lower weekend concentrations were observed. The NOx concentrations from the TR sites remain unchanged in the majority of the cities over the study period. When stratified by 3 time periods according to the implementation of the EURO standards, an increasing NO2/NOx ratio in 7/9 cities with time was noted. However, over the same time period the NO/NO2 ratio decreased in 8/9 cities. A permanent inversion of the NO/NO2 ratio was observed to occur in 2003 in 5/9 cities. Our analyses of temporal and diurnal patterns of NOx in European cities show reductions in concentrations consistent with reductions in primary emissions likely arising from the implementation of successive EURO standards. The generally constant or increasing NO2 concentrations in the majority of the cities assessed over the study period underline the need of further regulative measures to meet the air quality standards and consequently to minimise adverse effects on human health. The ongoing collection and analysis of pollution concentrations across

  10. Measurement of offline exhaled nitric oxide in a study of community exposure to air pollution.

    PubMed Central

    Koenig, J Q; Jansen, K; Mar, T F; Lumley, T; Kaufman, J; Trenga, C A; Sullivan, J; Liu, L-J S; Shapiro, G G; Larson, T V

    2003-01-01

    As part of a large panel study in Seattle, Washington, we measured levels of exhaled nitric oxide (eNO) in children's homes and fixed-site particulate matter with aerodynamic diameters of 2.5 micro m or less (PM(2.5)) outside and inside the homes as well as personal PM(2.5) during winter and spring sessions of 2000-2001. Nineteen subjects 6-13 years of age participated; 9 of the 19 were on inhaled corticosteroid (ICS) therapy. Exhaled breath measurements were collected offline into a Mylar balloon for up to 10 consecutive days. Mean eNO values were 19.1 (SD +/- 11.4) ppb in winter sessions and 12.5 +/- 6.6 ppb in spring sessions. Fixed-site PM(2.5) mean concentrations were 10.1 +/- 5.7 microg/m(3) outside homes and 13.3 +/- 1.4 inside homes; the personal PM(2.5) mean was 13.4 +/- 3.2 microg/m(3). We used a linear mixed-effects model with random intercept and an interaction term for medications to test for within-subject-within-session associations between eNO and various PM(2.5) values. We found a 10 microg/m(3) increase in PM(2.5) from the outdoor, indoor, personal, and central-site measurements that was associated with increases in eNO in all subjects at lag day zero. The effect was 4.3 ppb [95% confidence interval (CI), 1.4-7.29] with the outdoor monitor, 4.2 ppb (95% CI, 1.02-7.4) for the indoor monitor, 4.5 ppb (95% CI, 1.02-7.9) with the personal monitor, and 3.8 ppb (95% CI, 1.2-6.4) for the central monitors. The interaction term for medication category (ICS users vs. nonusers) was significant in all analyses. These findings suggest that eNO can be used as an assessment tool in epidemiologic studies of health effects of air pollution. PMID:14527842

  11. Sliding durability of two carbide-oxide candidate high temperature fiber seal materials in air to 900 C

    NASA Technical Reports Server (NTRS)

    Dellacorte, Christopher; Steinetz, Bruce M.

    1992-01-01

    A test program to determine the friction and wear properties of two complex carbide oxide ceramic fibers for high temperature sliding seal applications is described. The fibers are based on Si, C, O, and Ti or Si, C, N, and O ceramic systems. Pin on disk tests using ceramic fiber covered pins and Inconel 718 disks, were conducted in air from 25 to 900 C to evaluate potential seal materials. This testing procedure was used in a previous study of oxide ceramic fibers which were found to exhibit wear behavior based predominantly on their mechanical properties. Like the oxide fibers tested previously, these carbide oxide ceramic fibers, show an increase in friction and wear with increased test temperature. At room temperature, the wear behavior seems to be based upon mechanical properties, namely tensile strength. At 500 and especially 900 C, the fibers wear by both mechanical fracture and by oxidative type wear. Based upon post test microscopic and x ray analyses, interaction between the fiber constituents and elements transferred from the counterface, namely Ni and Cr, may have occurred enhancing the tribochemical wear process. These results are interpreted.

  12. Oxidation rate of nuclear-grade graphite NBG-18 in the kinetic regime for VHTR air ingress accident scenarios

    NASA Astrophysics Data System (ADS)

    Lee, Jo Jo; Ghosh, Tushar K.; Loyalka, Sudarshan K.

    2013-07-01

    One of the most severe accident scenarios anticipated for VHTRs is an air ingress accident caused by a pipe break. Graphite oxidation could be severe under these conditions. In this work, the oxidation rate of NBG-18 nuclear-grade graphite was studied thermogravimetrically for different oxygen concentrations and with temperatures from 873 to 1873 K. A semi-empirical Arrhenius rate equation was developed for the temperature range of 873-1023 K. The activation energy of NBG-18 was 187 kJ/mol and the order of reaction was 1.25. The penetration depth of oxidant was about 3-4 mm for NBG-18 oxidized at 973 K. Increased porosity and changes in external geometry became more prominent at higher temperatures from about 1173 to 1873 K. The surface of oxidized NBG-18 was characterized by SEM, EDS, FTIR and XPS. Diffusion of oxygen to the graphite surface and walls of open volume pores. Adsorption of oxygen atoms on the graphite surface free active sites and complexes inducing the simultaneous forming of Csbnd O and Csbnd H bonds and breaking of Csbnd C bonds (dissociative chemisorption). Chemical reactions occur at the surface. Desorption of gaseous products, CO and CO2, from the graphite surface and transport to the bulk gas mixture.

  13. Developing Oxidized Nitrogen Atmospheric Deposition Source Attribution from CMAQ for Air-Water Trading for Chesapeake Bay

    NASA Astrophysics Data System (ADS)

    Dennis, R. L.; Napelenok, S. L.; Linker, L. C.; Dudek, M.

    2012-12-01

    Estuaries are adversely impacted by excess reactive nitrogen, Nr, from many point and nonpoint sources, including atmospheric deposition to the watershed and the estuary itself as a nonpoint source. For effective mitigation, trading among sources of Nr is being considered. The Chesapeake Bay Program is working to bring air into its trading scheme, which requires some special air computations. Airsheds are much larger than watersheds; thus, wide-spread or national emissions controls are put in place to achieve major reductions in atmospheric Nr deposition. The tributary nitrogen load reductions allocated to the states to meet the TMDL target for Chesapeake Bay are large and not easy to attain via controls on water point and nonpoint sources. It would help the TMDL process to take advantage of air emissions reductions that would occur with State Implementation Plans that go beyond the national air rules put in place to help meet national ambient air quality standards. There are still incremental benefits from these local or state-level controls on atmospheric emissions. The additional air deposition reductions could then be used to offset water quality controls (air-water trading). What is needed is a source to receptor transfer function that connects air emissions from a state to deposition to a tributary. There is a special source attribution version of the Community Multiscale Air Quality model, CMAQ, (termed DDM-3D) that can estimate the fraction of deposition contributed by labeled emissions (labeled by source or region) to the total deposition across space. We use the CMAQ DDM-3D to estimate simplified state-level delta-emissions to delta-atmospheric-deposition transfer coefficients for each major emission source sector within a state, since local air regulations are promulgated at the state level. The CMAQ 4.7.1 calculations are performed at a 12 km grid size over the airshed domain covering Chesapeake Bay for 2020 CAIR emissions. For results, we first present

  14. Oxidation chemistry of chloric acid in NOx/SOx and air toxic metal removal from gas streams

    SciTech Connect

    Kaczur, J.J.

    1996-12-31

    Chloric acid, HClO{sub 3}, is a new oxidizer which has recently been shown to be an effective agent in the simultaneous removal of NOx and/or SOx from combustion flue gases and various chemical processes, including nitrations and metal pickling. Aqueous chloric acid readily reacts with NO and SO{sub 2} even in dilute solutions at ambient temperatures. Chlorine dioxide, ClO{sub 2}, is formed as a chemical intermediate in the solution phase oxidation reactions. The oxidation by-products of NO include NO{sub 2} and nitric acid. The ClO{sub 2} generated from the solution phase reactions also participates in gas phase oxidation reactions with NO and NO{sub 2}. The combined solution phase and fast gas phase reaction chemistries provide the means for creating a new type of high performance NOx/SOx removal process. Wet scrubber based pilot plant tests have demonstrated up to 99% removal of NO. Additional recent research work has shown that chloric acid is an effective reagent for the removal of air toxic metals, such as elemental mercury, which are present in the waste gas output streams from incinerators, hydrogen from mercury cell chlor-alkali plants, and flue gases of coal-fired power plants. Work in this area is being conducted by Argonne National Laboratories and Olin. This paper discusses the oxidation chemistry of chloric acid and its unique solution and gas phase reactions with NO, SO{sub 2}, and air toxics in wet scrubber type process equipment. 32 refs., 16 figs., 5 tabs.

  15. Experimental and theoretical study of the oxidation of ventilation air methane over Fe2O3 and CuO.

    PubMed

    Jin, Yonggang; Sun, Chenghua; Su, Shi

    2015-07-01

    Coal mine ventilation air methane (VAM) is an important contributor to methane emissions from the energy sector. Although various technologies are under development, treatment of the VAM with an efficient and cost-effective approach has been an ongoing challenge due to massive flow rates of the ventilation air and low and variable methane concentrations. Recently a new concept based on the principle of chemical looping combustion (CLC) has been proposed for VAM abatement (Appl. Energy, 2014, 113, 1916), in which oxidation of low-concentration CH4 balanced by N2 with Fe2O3 or CuO as the oxygen carrier was studied. Here, we thoroughly examined the feasibility of CLC of VAM based on experimental study and theoretical calculations. Reduction of Fe2O3 and CuO and evolution of gas products during CH4 oxidation were investigated using TGA-MS under two reaction atmospheres: 1 vol% CH4 balanced by N2 and the simulated VAM containing 1 vol% CH4, 20 vol% O2, 0.4 vol% CO2 and balance N2. It was found that the CLC of VAM is fundamentally infeasible because the reduced phase of Fe2O3 and CuO cannot be formed for chemical looping when reacting with the simulated VAM containing abundant oxygen. Theoretical calculations revealed that Fe2O3 and CuO remain stable without the transition to the reduced phase as the generated oxygen vacancy on the surface of metal oxides during CH4 oxidation can recover quickly with O2 adsorption and dissociation. Calculations confirmed that both Fe2O3 and CuO play a role of surface catalyst in VAM oxidation. More importantly, it was found that the low-coordinated metal atoms and oxygen vacancies can stabilize CHx radicals to promote the dissociation of CH4, which is generally the rate-determining step for CH4 oxidation. Such findings are useful for new development and understanding of high-performance and low-cost metal oxide catalysts for CH4 oxidation. PMID:26028316

  16. Wet air oxidation for the treatment of industrial wastes. Chemical aspects, reactor design and industrial applications in Europe

    SciTech Connect

    Debellefontaine, H.; Foussard, J.N.

    2000-07-01

    Aqueous wastes containing organic pollutants can be efficiently treated by wet air oxidation (WAO), i.e., oxidation (or combustion) by molecular oxygen in the liquid phase, at high temperature (200--325 C) and pressure (up to 175 bar). This method is suited to the elimination of special aqueous wastes from the chemical industry as well as to the treatment of domestic sludge. It is an enclosed process, with a limited interaction with the environment, as opposed to incineration. Usually, the operating cost is lower than 95 Euro M{sup {minus}3} and the preferred COD load ranges from 10 to 80 kg m{sup {minus}3}. Only a handful of industrial reactors are in operation world-wide, mainly because of the high capital investment they require. This paper reviews the major results obtained with the WAO process and assess its field of possible application to industrial wastes. In addition, as only a very few studies have been devoted to the scientific design of such reactors (bubble columns), what needs to be known for this scientific design is discussed. At present, a computer program aimed at determining the performance of a wet air oxidation reactor depending on the various operating parameters has been implemented at the laboratory. Some typical results are presented, pointing out the most important parameters and the specific behavior of these units.

  17. Mechanical performance of reactive-air-brazed (RAB) ceramic/metal joints for solid oxide fuel cells at ambient temperature

    NASA Astrophysics Data System (ADS)

    Kuhn, B.; Wetzel, F. J.; Malzbender, J.; Steinbrech, R. W.; Singheiser, L.

    Mechanical integrity of the sealants in planar SOFC stacks is a key prerequisite for reliable operation. In this respect joining with metals rather than brittle glass-ceramics is considered to have advantages. Hence, as one of the joining solutions for SOFCs of planar design, reactive air brazing of ceramic cells into metallic frames gains increasing interest. Fracture experiments are carried out to characterize fracture energy and failure mechanisms of silver-based reactive-air-brazes, used for joining the zirconia electrolytes of anode supported planar cells with metallic Crofer22APU frames. The specimens are mechanically tested in notched beam bending geometry. In-situ observation in optical and SEM resolution reveals specific failure mechanisms. The influence of braze formulation and associated interfacial reactions on the crack path location is addressed. Discussion of the results focuses in particular on the role of oxide scale formation.

  18. Oxidation mechanisms of CF2Br2 and CH2Br2 induced by air nonthermal plasma.

    PubMed

    Schiorlin, Milko; Marotta, Ester; Dal Molin, Marta; Paradisi, Cristina

    2013-01-01

    Oxidation mechanisms in air nonthermal plasma (NTP) at room temperature and atmospheric pressure were investigated in a corona reactor energized by +dc, -dc, or +pulsed high voltage.. The two bromomethanes CF(2)Br(2) and CH(2)Br(2) were chosen as model organic pollutants because of their very different reactivities with OH radicals. Thus, they served as useful mechanistic probes: they respond differently to the presence of humidity in the air and give different products. By FT-IR analysis of the postdischarge gas the following products were detected and quantified: CO(2) and CO in the case of CH(2)Br(2), CO(2) and F(2)C ═ O in the case of CF(2)Br(2). F(2)C ═ O is a long-lived oxidation intermediate due to its low reactivity with atmospheric radicals. It is however removed from the NTP processed gas by passage through a water scrubber resulting in hydrolysis to CO(2) and HF. Other noncarbon containing products of the discharge were also monitored by FT-IR analysis, including HNO(3) and N(2)O. Ozone, an important product of air NTP, was never detected in experiments with CF(2)Br(2) and CH(2)Br(2) because of the highly efficient ozone depleting cycles catalyzed by BrOx species formed from the bromomethanes. It is concluded that, regardless of the type of corona applied, CF(2)Br(2) reacts in air NTP via a common intermediate, the CF(2)Br radical. The possible reactions leading to this radical are discussed, including, for -dc activation, charge exchange with O(2)(-), a species detected by APCI mass spectrometry. PMID:23190335

  19. Stressed-Oxidation Lifetime of Different SiC Fiber, CVI Matrix SiC Minicomposites in Air

    NASA Technical Reports Server (NTRS)

    Morscher, Gregory N.; Martinez-Fernandez, Julian

    1998-01-01

    The stressed-oxidation lifetime properties of several minicomposites composed of single fiber tows with a CVI SiC matrix were compared. The minicomposites were made up of Nicalon(Tm) and Hi-Nicalon(Tm) SiC fibers with carbon or BN interphases. Constant load stress-rupture tests were performed between 600 and 13000 C in air for all of the minicomposite systems. Cyclic load testing was performed on the Hi-Nicalon minicomposite systems. The factors controlling the different lifetime behaviors: fiber rupture properties, interphase oxidation, fiber degradation, and fiber-matrix bonding, are discussed in light of different minicomposite constituents. All of the systems were subject to intermediate temperature embrittlement. The Hi-Nicalon fiber, BN interphase system, performed the best for constant load conditions. For cyclic load conditions, both the BN- interphase and C-interphase minicomposites displayed poor, but different failure behavior.

  20. Nanoporous silicon prepared through air-oxidation demagnesiation of Mg2Si and properties of its lithium ion batteries.

    PubMed

    Liang, Jianwen; Li, Xiaona; Hou, Zhiguo; Guo, Cong; Zhu, Yongchun; Qian, Yitai

    2015-04-28

    Nanoporous silicon has been prepared through the air-oxidation demagnesiation of Mg2Si at 600 °C for 10 hours (Mg2Si + O2 → Si + MgO), followed by HCl washing. Mg2Si was prepared from 200 mesh commercial Si at 500 °C for 5 h in an autoclave. The as-prepared Si exhibits a reversible capacity of 1000 mA h g(-1) at 36 A g(-1) and ∼1200 mA h g(-1) at 1.8 A g(-1) over 400 cycles. PMID:25812916

  1. National emission standards for hazardous air pollutants for ethylene oxide commercial sterilization and fumigation operations--EPA. Interim final rule.

    PubMed

    1998-12-01

    Today's action suspends the National Emission Standards for Hazardous Air Pollutants for Ethylene Oxide Commercial Sterilization and Fumigation Operations (EO NESHAP) requirements for chamber exhaust and aeration room vents. The suspension allows affected sources subject to the EO NESHAP to defer compliance with the NESHAP requirements for chamber exhaust and aeration room vents for one year until December 6, 1999. This suspension does not affect the requirement for sources subject to the EO NESHAP to comply with provisions for sterilizer vents by December 6, 1998. This action does not change the level of the standards or the intent of the NESHAP promulgated in 1994. PMID:10338881

  2. Prediction of hydrodynamics and chemistry of confined turbulent methane-air flames with attention to formation of oxides of nitrogen

    NASA Technical Reports Server (NTRS)

    Elghobashi, S.; Spalding, D. B.; Srivatsa, S. K.

    1977-01-01

    A formulation of the governing partial differential equations for fluid flow and reacting chemical species in a tubular combustor is presented. A numerical procedure for the solution of the governing differential equations is described, and models for chemical equilibrium and chemical kinetics calculations are presented. The chemical equilibrium model is used to characterize the hydrocarbon reactions. The chemical kinetics model is used to predict the concentrations of the oxides of nitrogen. The combustor consists of a cylindrical duct of varying cross sections with concentric streams of gaseous fuel and air entering the duct at one end. Four sample cases with specified inlet and boundary conditions are considered, and the results are discussed

  3. OXIDATIVE STRESS MEDIATES AIR POLLUTION PARTICLE-INDUCED ACUTE LUNG INJURY AND MOLECULAR PATHOLOGY

    EPA Science Inventory

    Abstract
    Insight into the mechanism(s) by which ambient air particulate matter (PM) mediates adverse health effects is needed to provide biological plausibility to epidemiological studies demonstrating associations between PM exposure and increased morbidity and mortality. Alt...

  4. Comparison of Short-Term Oxidation Behavior of Model and Commercial Chromia-Forming Ferritic Stainless Steels in Air with Water Vapor

    SciTech Connect

    Brady, Michael P; Keiser, James R; More, Karren Leslie; Fayek, Mostafa; Walker, Larry R; Meisner, Roberta Ann; Anovitz, Lawrence {Larry} M; Wesolowski, David J; Cole, David R

    2012-01-01

    A high-purity Fe-20Cr and commercial type 430 ferritic stainless steel were exposed at 700 and 800 C in dry air and air with 10% water vapor (wet air) and characterized by SEM, XRD, STEM, SIMS, and EPMA. The Fe-20Cr alloy formed a fast growing Fe-rich oxide scale at 700 C in wet air after 24 h exposure, but formed a thin chromia scale at 700 C in dry air and at 800 C in both dry air and wet air. In contrast, thin spinel + chromia base scales with a discontinuous silica subscale were formed on 430 stainless steel under all conditions studied. Extensive void formation was observed at the alloy-oxide interface for the Fe-20Cr in both dry and wet conditions, but not for the 430 stainless steel. The Fe-20Cr alloy was found to exhibit a greater relative extent of subsurface Cr depletion than the 430 stainless steel, despite the former's higher Cr content. Depletion of Cr in the Fe-20Cr after 24 h exposure was also greater at 700 C than 800 C. The relative differences in oxidation behavior are discussed in terms of the coarse alloy grain size of the high-purity Fe-20Cr material, and the effects of Mn, Si, and C on the oxide scale formed on the 430 stainless steel.

  5. Oxidation rate of graphitic matrix material in the kinetic regime for VHTR air ingress accident scenarios

    NASA Astrophysics Data System (ADS)

    Lee, Jo Jo; Ghosh, Tushar K.; Loyalka, Sudarshan K.

    2014-08-01

    Data on oxidation rates of matrix-grade graphite in the kinetically-controlled temperature regime of graphite oxidation are needed for safety analysis of High Temperature Gas Cooled Reactors and Very High Temperature Reactors. In this work, the oxidation rate of graphitic matrix material GKrS was measured thermogravimetrically for various oxygen concentrations and with temperatures from 873 to 1873 K. A semi-empirical Arrhenius rate equation was also developed for this temperature range. The activation energy of the graphitic material is found to be about 111.5 kJ/mol. The order of reaction was found to be about 0.89. The surface of oxidized GKrS was characterized by Scanning Electron Microscopy, Electron Dispersive Spectroscopy, Fourier Transform Infrared Spectroscopy and X-ray Photoelectron Spectroscopy.

  6. AIR QUALITY CRITERIA FOR OZONE AND OTHER PHOTOCHEMICAL OXIDANTS. VOLUME 3.

    EPA Science Inventory

    Selected scientific information through early 1985 is presented and evaluated relative to the health and welfare effects associated with exposure to ozone and other photochemical oxidants. Data on health and welfare effects are emphasized; additional information is provided for u...

  7. CATALYTIC OXIDATION OF AIR POLLUTANTS FROM PULP AND PAPER INDUSTRY USING OZONE

    EPA Science Inventory

    Major pollutants from pulp and paper mills include volatile organic compounds (VOCs) such as methanol and total reduced sulfur compounds (TRS) such as dimethyl sulfide. The conventional treatment technologies including incineration or catalytic thermal oxidation are energy intens...

  8. Air oxidation of hydrazine. 1. Reaction kinetics on natural kaolinites, halloysites, and model substituent layers with varying iron and titanium oxide and O- center contents

    NASA Technical Reports Server (NTRS)

    Coyne, L.; Mariner, R.; Rice, A.

    1991-01-01

    Air oxidation of hydrazine was studied by using a group of kaolinites, halloysites, and substituent oxides as models for the tetrahedral and octahedral sheets. The rate was found to be linear with oxygen. The stoichiometry showed that oxygen was the primary oxidant and that dinitrogen was the only important nitrogen-containing product. The rates on kaolinites were strongly inhibited by water. Those on three-dimensional silica and gibbsite appeared not to be. That on a supposedly layered silica formed from a natural kaolinite by acid leaching showed transitional behavior--slowed relative to that expected from a second-order reaction relative to that on the gibbsite and silica but faster than those on the kaolinites. The most striking result of the reaction was the marked increase in the rate of reaction of a constant amount of hydrazine as the amount of clay was increased. The increase was apparent (in spite of the water inhibition at high conversions) over a 2 order of magnitude variation of the clay weight. The weight dependence was taken to indicate that the role of the clay is very important, that the number of reactive centers is very small, or that they may be deactivated over the course of the reaction. In contrast to the strong dependence on overall amount of clay, the variation of amounts of putative oxidizing centers, such as structural Fe(III), admixed TiO2 or Fe2O3, or O- centers, did not result in alteration of the rate commensurate with the degree of variation of the entity in question. Surface iron does play some role, however, as samples that were pretreated with a reducing agent were less active as catalysts than the parent material. These results were taken to indicate either that the various centers interact to such a degree that they cannot be considered independently or that the reaction might proceed by way of surface complexation, rather than single electron transfers.

  9. Enhanced oxidation of air contaminants on an ultra-low density UV-accessible aerogel photocatalyst

    SciTech Connect

    Dreyer, M.; Newman, G.K.; Lobban, L.; Kersey, S.J.; Wang, R.; Harwell, J.H.

    1997-12-31

    This research developed new forms of photocatalysts that could potentially move photocatalytic degradation of air contaminants into the main stream of industrially used remediation technologies. Tests of the photocatalytic activity of the TiO{sub 2} aerogel catalysts have been carried out using both acetone and methane as the air contaminant. For comparison, the same tests were carried out on a standard (non-aerogel) anatase powder. Despite having very low crystallinity, the aerogel decontaminates the air far more effectively than an equal volume of the anatase powder which indicates that a much larger fraction of the aerogel is activated by the UV light. Experimental data were used to determine adsorption equilibrium constants for acetone, and to determine reaction rate constants assuming a Langmuir-Hinshelwood type rate expression.

  10. Impact of Air Filter Material on Metal Oxide Semiconductor (MOS) Device Characteristics in HF Vapor Environment

    NASA Astrophysics Data System (ADS)

    Hsiao, Chih-Wen; Lou, Jen-Chung; Yeh, Ching-Fa; Hsieh, Chih-Ming; Lin, Shiuan-Jeng; Kusumi, Toshio

    2004-05-01

    Airborne molecular contamination (AMC) is becoming increasingly important as devices are scaled down to the nanometer generation. Optimum ultra low penetration air (ULPA) filter technology can eliminate AMC. In a cleanroom, however, the acid vapor generated from the cleaning process may degrade the ULPA filter, releasing AMC to the air and the surface of wafers, degrading the electrical characteristics of devices. This work proposes the new PTFE ULPA filter, which is resistant to acid vapor corrosion, to solve this problem. Experimental results demonstrate that the PTFE ULPA filter can effectively eliminate the AMC and provide a very clean cleanroom environment.

  11. A dose-controlled system for air-liquid interface cell exposure and application to zinc oxide nanoparticles

    PubMed Central

    2009-01-01

    Background Engineered nanoparticles are becoming increasingly ubiquitous and their toxicological effects on human health, as well as on the ecosystem, have become a concern. Since initial contact with nanoparticles occurs at the epithelium in the lungs (or skin, or eyes), in vitro cell studies with nanoparticles require dose-controlled systems for delivery of nanoparticles to epithelial cells cultured at the air-liquid interface. Results A novel air-liquid interface cell exposure system (ALICE) for nanoparticles in liquids is presented and validated. The ALICE generates a dense cloud of droplets with a vibrating membrane nebulizer and utilizes combined cloud settling and single particle sedimentation for fast (~10 min; entire exposure), repeatable (<12%), low-stress and efficient delivery of nanoparticles, or dissolved substances, to cells cultured at the air-liquid interface. Validation with various types of nanoparticles (Au, ZnO and carbon black nanoparticles) and solutes (such as NaCl) showed that the ALICE provided spatially uniform deposition (<1.6% variability) and had no adverse effect on the viability of a widely used alveolar human epithelial-like cell line (A549). The cell deposited dose can be controlled with a quartz crystal microbalance (QCM) over a dynamic range of at least 0.02-200 μg/cm2. The cell-specific deposition efficiency is currently limited to 0.072 (7.2% for two commercially available 6-er transwell plates), but a deposition efficiency of up to 0.57 (57%) is possible for better cell coverage of the exposure chamber. Dose-response measurements with ZnO nanoparticles (0.3-8.5 μg/cm2) showed significant differences in mRNA expression of pro-inflammatory (IL-8) and oxidative stress (HO-1) markers when comparing submerged and air-liquid interface exposures. Both exposure methods showed no cellular response below 1 μg/cm2 ZnO, which indicates that ZnO nanoparticles are not toxic at occupationally allowed exposure levels. Conclusion The ALICE

  12. Studies on the regeneration of sulfided iron oxide sorbent with steam-air mixtures. Final technical report

    SciTech Connect

    Tamhankar, S.S.

    1982-10-01

    The work reported here was performed as a continuation of studies conducted previously at West Virginia University (WVU), Department of Chemical Engineering on a hot-fuel-gas desulfurization process using a regenerable iron oxide-silica sorbent. The overall process consists of two stages: the absorption or the H/sub 2/S removal stage and the sorbent regeneration stage. In the absorption stage the iron oxide reacts with H/sub 2/S to form iron sulfide. For regeneration of the sulfided sorbent, various schemes have been proposed. Studies at WVU have been aimed at identifying the important reactions involved in absorption and regeneration stages, elucidating their mechanisms and investigating detailed kinetics. In the first two phases of the study, reactions in H/sub 2/S absorption and in sorbent regeneration by air/SO/sub 2/ were investigated. This report addresses regeneration of the sulfided sorbent using steam-air mixtures. Experiments were conducted in a thermo-gravimetric analyzer (TGA) apparatus. The weight changes were recorded as a function of time during the reactions of iron sulfide (in the presulfided sorbent) with nitrogen-stream and air-steam mixtures. In addition, several solid samples at different conversion levels were anlayzed by LECO sulfur anlaysis technique and by Mossbauer spectroscopy. Based on these results, a reaction mechanism has been postulated. Additional work is necessary to investigate the gas-phase reactions which may be taking place simultaneously in a fixed - or a fluidized-bed reactor, and to formulate the overall reaction scheme. 14 figures, 3 tables.

  13. Introduction of thiol moieties, including their thiol-ene reactions and air oxidation, onto polyelectrolyte multilayer substrates.

    PubMed

    Madaan, Nitesh; Romriell, Naomi; Tuscano, Joshua; Schlaad, Helmut; Linford, Matthew R

    2015-12-01

    We describe the derivatization of uncross-linked and cross-linked layer-by-layer (LbL) assemblies of polyelectrolytes (polyallylamine hydrochloride and polyacrylic acid) with sulfydryl groups via Traut's reagent (2-iminothiolane). This thiolation was optimized with regards to temperature, concentration, and pH. The stability of the resulting -SH groups in the air was determined by X-ray photoelectron spectroscopy (XPS). This air oxidation has obvious implications for the use of thiol-ene reactions in materials chemistry, and there appears to be little on this topic in the literature. Three main S 2s signals were observed by XPS: at 231.5 eV (oxidized sulfur), 227.6 eV (thiol groups), and 225.4 eV (thiolate groups). Due to their rapid oxidation, we recommend that thiolated surfaces be used immediately after they are prepared. As driven by 254 nm UV light, thiol groups on polyelectrolyte multilayers react with 1,2-polybutadiene (PBd), and residual carbon-carbon double bonds on adsorbed PBd similarly react with another thiol. In the case of a fluorinated thiol, surfaces with high water contact angles (ca. 120°) are obtained. Modest exposures to light result in derivatization, while longer exposures damage the assemblies. Polyelectrolyte-thiol-PBd-thiol assemblies delaminate from their substrates when immersed for long periods of time in water. Surface silanization with an amino silane prevents this delamination and leads to stable assemblies. These assemblies withstand various stability tests. Techniques used to analyze the materials in this study include X-ray photoelectron spectroscopy (XPS), spectroscopic ellipsometry (SE), atomic force microscopy (AFM), and contact angle goniometry. PMID:26295196

  14. 78 FR 47253 - Approval and Promulgation of Air Quality Implementation Plans; Maine; Oxides of Nitrogen...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-08-05

    ... (69 FR 23951) requires areas to request a separate section 182(f) NO X exemption request under the...: (1) The NO X SIP call (63 FR 57356: October 27, 1998); (2) the Clean Air Interstate Rule (CAIR) (70..., 1996 (61 FR 5690). If EPA takes final action to approve Maine's section 182(f) NO X exemption...

  15. High-Temperature Oxidation and Decarburization of 14.55 wt pct Cr-Cast Iron in Dry Air Atmosphere

    NASA Astrophysics Data System (ADS)

    Efremenko, V. G.; Chabak, Yu. G.; Lekatou, A.; Karantzalis, A. E.; Efremenko, A. V.

    2016-04-01

    The oxidation and decarburization behavior of 14.55 wt pct Cr-cast iron at 1273 K to 1423 K (1000 °C to 1150 °C) in a dry air atmosphere was studied. A gravimetric investigation showed that intensive oxidation of cast iron takes place at temperatures above 1273 K (1000 °C). It is found that oxidizing heating is accompanied by decarburization, which manifests itself in secondary and eutectic carbide dissolution. The volume fraction of carbides decreases with temperature and holding duration increasing. Decarburization results in the formation of a decarburized layer up to 4 mm in depth. A carbide-free layer in depth up to 100 μm appears in the free surface after 6 to 8 hours holding at 1373 K to 1423 K (1100 °C to 1150 °C). Preliminary activation energy calculations suggested that the eutectic carbide dissolution at the depths of 50 to 400 μm is controlled by carbon diffusion in austenite. The dissolution of eutectic carbides involves a capillarity-induced mechanism, which consists of formation and growth of capillary cavities inside carbides.

  16. Speciation and Fate of Trace Metals in Estuarine Sediments Under Reduced and Oxidized Conditions, Seaplane Lagoon, Alameda Naval Air Station

    SciTech Connect

    Carroll, S A; Day, P A; Esser, B; Randall, S

    2002-10-18

    We have identified important chemical reactions that control the fate of metal-contaminated estuarine sediments if they are left undisturbed (in situ) or if they are dredged. We combined information on the molecular bonding of metals in solids from X-ray absorption spectroscopy (XAS) with thermodynamic and kinetic driving forces obtained from dissolved metal concentrations to deduce the dominant reactions under reduced and oxidized conditions. We evaluated the in situ geochemistry of metals (cadmium, chromium, iron, lead, manganese and zinc) as a function of sediment depth (to 100 cm) from a 60-year record of contamination at the Alameda Naval Air Station, California. Results from XAS and thermodynamic modeling of porewaters show that cadmium and most of the zinc form stable sulfide phases, and that lead and chromium are associated with stable carbonate, phosphate, phyllosilicate, or oxide minerals. Therefore, there is minimal risk associated with the release of these trace metals from the deeper sediments contaminated prior to the Clean Water Act (1975) as long as reducing conditions are maintained. Increased concentrations of dissolved metals with depth were indicative of the formation of metal HS- complexes. The sediments also contain zinc, chromium, and manganese associated with detrital iron-rich phyllosilicates and/or oxides. These phases are recalcitrant at near-neutral pH and do not undergo reductive dissolution within the 60-year depositional history of sediments at this site. The fate of these metals during dredging was evaluated by comparing in situ geochemistry with that of sediments oxidized by seawater in laboratory experiments. Cadmium and zinc pose the greatest hazard from dredging because their sulfides were highly reactive in seawater. However, their dissolved concentrations under oxic conditions were limited eventually by sorption to or co-precipitation with an iron (oxy)hydroxide. About 50% of the reacted CdS and 80% of the reacted ZnS were

  17. Parametric Evaluation of an Innovative Ultra-Violet PhotocatalyticOxidation (UVPCO) Air Cleaning Technology for Indoor Applications

    SciTech Connect

    Hodgson, Alfred T.; Sullivan, Douglas P.; Fisk, William J.

    2005-10-31

    An innovative Ultra-Violet Photocatalytic Oxidation (UVPCO) air cleaning technology employing a semitransparent catalyst coated on a semitransparent polymer substrate was evaluated to determine its effectiveness for treating mixtures of volatile organic compounds (VOCs) representative of indoor environments at low, indoor-relevant concentration levels. The experimental UVPCO contained four 30 by 30-cm honeycomb monoliths irradiated with nine UVA lamps arranged in three banks. A parametric evaluation of the effects of monolith thickness, air flow rate through the device, UV power, and reactant concentrations in inlet air was conducted for the purpose of suggesting design improvements. The UVPCO was challenged with three mixtures of VOCs. A synthetic office mixture contained 27 VOCs commonly measured in office buildings. A building product mixture was created by combining sources including painted wallboard, composite wood products, carpet systems, and vinyl flooring. The third mixture contained formaldehyde and acetaldehyde. Steady state concentrations were produced in a classroom laboratory or a 20-m{sup 3} chamber. Air was drawn through the UVPCO, and single-pass conversion efficiencies were measured from replicate samples collected upstream and downstream of the reactor. Thirteen experiments were conducted in total. In this UVPCO employing a semitransparent monolith design, an increase in monolith thickness is expected to result in general increases in both reaction efficiencies and absolute reaction rates for VOCs oxidized by photocatalysis. The thickness of individual monolith panels was varied between 1.2 and 5 cm (5 to 20 cm total thickness) in experiments with the office mixture. VOC reaction efficiencies and rates increased with monolith thickness. However, the analysis of the relationship was confounded by high reaction efficiencies in all configurations for a number of compounds. These reaction efficiencies approached or exceeded 90% for alcohols, glycol

  18. MIXTURE EFFECTS IN THE CATALYTIC OXIDATION OF VOCS (VOLATILE ORGANIC COMPOUNDS) IN AIR

    EPA Science Inventory

    The report gives results of a study of the deep oxidation of organic mixtures over a heterogeneous catalyst in an attempt to explain earlier observations concerning the apparent inhibition or enhancement of destruction of some components to establish a scientific basis for the de...

  19. Differences between the oxidation behaviour of A3 fuel element matrix graphites in air and in steam and its relevance on accident progress in HTRs

    SciTech Connect

    Kuehn, K.; Hinssen, H-K.; Moormann, R.

    2004-07-01

    The fuel element matrix graphites A3-3 and A3-27 were used in High Temperature Reactor fuel pebbles for many years. However, these materials show as other graphites a limited oxidation resistance in contact to oxidising gases (air and steam), which even decreases with increasing temperatures: In HTRs, having in normal operation a non-oxidising environment, an ingress of air or steam leads to corrosion of graphite with the potential of enhanced fission product release Matrix graphites differ by its coked binder content from standard nuclear graphites (e.g. V483T, ASR-1RG, IG110, H-451), where both filler and binder are completely graphitized. The influence of this coked binder content on the oxidation behaviour will be discussed in this paper. Experimental investigations with A3-3 and A3-27 were done in oxygen (air) at temperatures between 673 - 1023 K and in steam between 1173 - 1253 K. These experiments took place under isothermal conditions in the chemical regime, where the chemical reaction itself is the rate limiting step and a homogeneous oxidation inside of the sample occurs. The experiments reveal different oxidation behaviour as well between binder and filler component as between oxidation behaviour in oxygen (air) and steam. In air at low temperatures two rate maxima are observed: The first maximum attend in all experiments at {approx} 5 % burn off, a second one at higher burn off values (35 - 45 % burn off). These rate maxima can be explained by a selective binder-filler oxidation: The first peak at 5 % burn off is due to the oxidation of the binder, the second peak at higher burn off values is caused by the oxidation of the remaining filler. At higher temperatures in air the filler peak becomes more pronounced and the binder peak vanishes, which is due to the lower activation energy of binder oxidation compared to the filler. In steam this behaviour appears contrary: A maximum at 5 % burn off, which is probably also connected to the binder, is observed

  20. Synergistic bifunctional catalyst design based on perovskite oxide nanoparticles and intertwined carbon nanotubes for rechargeable zinc-air battery applications.

    PubMed

    Lee, Dong Un; Park, Hey Woong; Park, Moon Gyu; Ismayilov, Vugar; Chen, Zhongwei

    2015-01-14

    Advanced morphology of intertwined core-corona structured bifunctional catalyst (IT-CCBC) is introduced where perovskite lanthanum nickel oxide nanoparticles (LaNiO3 NP) are encapsulated by high surface area network of nitrogen-doped carbon nanotubes (NCNT) to produce highly active and durable bifunctional catalyst for rechargeable metal-air battery applications. The unique composite morphology of IT-CCBC not only enhances the charge transport property by providing rapid electron-conduction pathway but also facilitates in diffusion of hydroxyl and oxygen reactants through the highly porous framework. Confirmed by electrochemical half-cell testing, IT-CCBC in fact exhibits very strong synergy between LaNiO3 NP and NCNT demonstrating bifunctionality with significantly improved catalytic activities of oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Furthermore, when compared to the state-of-art catalysts, IT-CCBC outperforms Pt/C and Ir/C in terms of ORR and OER, respectively, and shows improved electrochemical stability compared to them after cycle degradation testing. The practicality of the catalyst is corroborated by testing in a realistic rechargeable zinc-air battery utilizing atmospheric air in ambient conditions, where IT-CCBC demonstrates superior charge and discharge voltages and long-term cycle stability with virtually no battery voltage fading. These improved electrochemical properties of the catalyst are attributed to the nanosized dimensions of LaNiO3 NP controlled by simple hydrothermal technique, which enables prolific growth of and encapsulation by highly porous NCNT network. The excellent electrochemical results presented in this study highlight IT-CCBC as highly efficient and commercially viable bifunctional catalyst for rechargeable metal-air battery applications. PMID:25494945

  1. Oxidation Resistance of Materials Based on Ti3AlC2 Nanolaminate at 600 °C in Air.

    PubMed

    Ivasyshyn, Andrij; Ostash, Orest; Prikhna, Tatiana; Podhurska, Viktoriya; Basyuk, Tatiana

    2016-12-01

    The oxidation behavior of Ti3AlC2-based materials had been investigated at 600 °C in static air for 1000 h. It was shown that the intense increase of weight gain per unit surface area for sintered material with porosity of 22 % attributed to oxidation of the outer surface of the specimen and surfaces of pores in the bulk material. The oxidation kinetics of the hot-pressed Ti3AlC2-based material with 1 % porosity remarkably increased for the first 15 h and then slowly decreased. The weight gain per unit surface area for this material was 1.0 mg/cm(2) after exposition for 1000 h. The intense initial oxidation of Ti3AlC2-based materials can be eliminated by pre-oxidation treatment at 1200 °C in air for 2 h. As a result, the weight gain per unit surface area for the pre-oxidized material did not exceed 0.11 mg/cm(2) after 1000 h of exposition at 600 °C in air. It was demonstrated that the oxidation resistance of Ti3AlC2-based materials can be significantly improved by niobium addition. PMID:27506531

  2. Response of ozone to changes in hydrocarbon and nitrogen oxide concentrations in outdoor smog chambers filled with Los Angeles air

    NASA Astrophysics Data System (ADS)

    Kelly, Nelson A.; Gunst, Richard F.

    During the summer portion of the 1987 Southern California Air Quality Study (SCAQS), outdoor smog chamber experiments were performed on Los Angeles air to determine the response of maximum ozone levels, O 3(max), to changes in the initial concentrations of hydrocarbons, HC, and nitrogen oxides, NO x. These captive-air experiments were conducted in downtown Los Angeles and in the downwind suburb of Claremont. Typically, eight chambers were filled with LA air in the morning. In some chambers the initial HC and/or NO x concentrations were changed by 25% to 50% by adding various combinations of a mixture of HC, clean air, or NO x. The O 3 concentration in each chamber was monitored throughout the day to determine O 3(max). An empirical mathematical model for O 3(max) was developed from regression fits to the initial HC and NO x concentrations and to the average daily temperature at both sites. This is the first time that a mathematical expression for the O 3-precursor relationship and the positive effect of temperature on O 3(max) have been quantified using captive-air experiments. An ozone isopleth diagram prepared from the empirical model was qualitatively similar to those prepared from photochemical mechanisms. This constitutes the first solely empirical corroboration of the O 3 contour shape for Los Angeles. To comply with the Federal Ozone Standard in LA, O 3(max) must be reduced by approximately 50%. Several strategies for reducing O 3(max) by 50% were evaluated using the empirical model. For the average initial conditions that we measured in LA, the most efficient strategy is one that reduces HC by 55-75%, depending on the ambient HC/NO x ratio. Any accompanying reduction in NO x would be counter-productive to the benefits of HC reductions. In fact, reducing HC and NO x simultaneously requires larger percentage reductions for both than the reduction required when HC alone is reduced. The HC-reduction strategy is the most efficient on average, but no single

  3. Gas phase formation of extremely oxidized pinene reaction products in chamber and ambient air

    NASA Astrophysics Data System (ADS)

    Ehn, M.; Kleist, E.; Junninen, H.; Petäjä, T.; Lönn, G.; Schobesberger, S.; Dal Maso, M.; Trimborn, A.; Kulmala, M.; Worsnop, D. R.; Wahner, A.; Wildt, J.; Mentel, Th. F.

    2012-06-01

    High molecular weight (300-650 Da) naturally charged negative ions have previously been observed at a boreal forest site in Hyytiälä, Finland. The long-term measurements conducted in this work showed that these ions are observed practically every night between spring and autumn in Hyytiälä. The ambient mass spectral patterns could be reproduced in striking detail during additional measurements of α-pinene (C10H16) oxidation at low-OH conditions in the Jülich Plant Atmosphere Chamber (JPAC). The ions were identified as clusters of the nitrate ion (NO3-) and α-pinene oxidation products reaching oxygen to carbon ratios of 0.7-1.3, while retaining most of the initial ten carbon atoms. Attributing the ions to clusters instead of single molecules was based on additional observations of the same extremely oxidized organics in clusters with HSO4- (Hyytiälä) and C3F5O2- (JPAC). The most abundant products in the ion spectra were identified as C10H14O7, C10H14O9, C10H16O9, and C10H14O11. The mechanism responsible for forming these molecules is still not clear, but the initial reaction is most likely ozone attack at the double bond, as the ions are mainly observed under dark conditions. β-pinene also formed highly oxidized products under the same conditions, but less efficiently, and mainly C9 compounds which were not observed in Hyytiälä, where β-pinene on average is 4-5 times less abundant than α-pinene. Further, to explain the high O/C together with the relatively high H/C, we propose that geminal diols and/or hydroperoxide groups may be important. We estimate that the night-time concentration of the sum of the neutral extremely oxidized products is on the order of 0.1-1 ppt (~106-107 molec cm-3). This is in a similar range as the amount of gaseous H2SO4 in Hyytiälä during day-time. As these highly oxidized organics are roughly 3 times heavier, likely with extremely low vapor pressures, their role in the initial steps of new aerosol particle formation and

  4. Gas phase formation of extremely oxidized pinene reaction products in chamber and ambient air

    NASA Astrophysics Data System (ADS)

    Ehn, M.; Kleist, E.; Junninen, H.; Petäjä, T.; Lönn, G.; Schobesberger, S.; Dal Maso, M.; Trimborn, A.; Kulmala, M.; Worsnop, D. R.; Wahner, A.; Wildt, J.; Mentel, Th. F.

    2012-02-01

    High molecular weight (300-650 Da) naturally charged negative ions have previously been observed at a boreal forest site in Hyytiälä, Finland. The long-term measurements conducted in this work showed that these ions are observed practically every night during spring and summer in Hyytiälä. The ambient mass spectral patterns could be reproduced in striking detail during additional measurements of α-pinene (C10H16) oxidation at low-OH conditions in the Jülich Plant Atmosphere Chamber (JPAC). The ions were identified as clusters of the nitrate ion (NO3-) and α-pinene oxidation products reaching oxygen to carbon ratios of 0.7-1.3, while retaining most of the initial ten carbon atoms. Attributing the ions to clusters instead of single molecules was based on additional observations of the same extremely oxidized organics in clusters with HSO4- (Hyytiälä) and C3F5O2- (JPAC). The most abundant products in the ion spectra were identified as C105H14O7, C10H14O9, C10H16O9, and C10H14O11. The mechanism responsible for forming these molecules is still not clear, but the initial reaction is most likely ozone attack at the double bond, as the ions are mainly observed under dark conditions. β-pinene also formed highly oxidized products under the same conditions, but less efficiently, and mainly C9 compounds which were not observed in Hyytiälä, where β-pinene on average is 4-5 times less abundant than α-pinene. Further, to explain the high O/C together with the relatively high H/C, we propose that geminal diols and/or hydroperoxide groups may be important. We estimate that the night-time concentration of the sum of the neutral extremely oxidized products is on the order of 0.1-1 ppt (~106-107 molec cm-3). This is in a similar range as the amount of gaseous H2SO4 in Hyytiälä during day-time. As these highly oxidized organics are roughly 3 times heavier, likely with extremely low vapor pressures, their role in the initial steps of new aerosol particle formation and

  5. Neutrophilic inflammatory response and oxidative stress in premenopausal women chronically exposed to indoor air pollution from biomass burning.

    PubMed

    Banerjee, Anirban; Mondal, Nandan Kumar; Das, Debangshu; Ray, Manas Ranjan

    2012-04-01

    The possibility of inflammation and neutrophil activation in response to indoor air pollution (IAP) from biomass fuel use has been investigated. For this, 142 premenopausal, never-smoking women (median age, 34 years) who cook exclusively with biomass (wood, dung, crop wastes) and 126 age-matched control women who cook with cleaner fuel liquefied petroleum gas (LPG) were enrolled. The neutrophil count in blood and sputum was significantly higher (p < 0.05) in biomass users than the control group. Flow cytometric analysis revealed marked increase in the surface expression of CD35 (complement receptor-1), CD16 (F(C)γ receptor III), and β(2) Mac-1 integrin (CD11b/CD18) on circulating neutrophils of biomass users. Besides, enzyme-linked immunosorbent assay showed that they had 72%, 67%, and 54% higher plasma levels of the proinflammatory cytokines tumor necrosis factor-alpha, interleukin-6, and interleukin-12, respectively, and doubled neutrophil chemoattractant interleukin-8. Immunocytochemical study revealed significantly higher percentage of airway neutrophils expressing inducible nitric oxide synthase, while the serum level of nitric oxide was doubled in women who cooked with biomass. Spectrophotometric analysis documented higher myeloperoxidase activity in circulating neutrophils of biomass users, suggesting neutrophil activation. Flow cytometry showed excess generation of reactive oxygen species (ROS) by leukocytes of biomass-using women, whereas their erythrocytes contained a depleted level of antioxidant enzyme superoxide dismutase (SOD). Indoor air of biomass-using households had two to four times more particulate matter with diameters of <10 μm (PM(10)) and <2.5 μm (PM(2.5)) as measured by real-time laser photometer. After controlling potential confounders, rise in proinflammatory mediators among biomass users were positively associated with PM(10) and PM(2.5) in indoor air, suggesting a close relationship between IAP and neutrophil activation. Besides

  6. Rate-ratio asymptotic analysis of methane-air diffusion-flame structure for predicting production of oxides of nitrogen

    SciTech Connect

    Hewson, J.C.; Williams, F.A.

    1999-05-01

    Production rates of oxides of nitrogen in laminar methane-air diffusion flames are addressed, with thermal, prompt, and nitrous oxide mechanisms taken into account, as well as consumption processes collectively termed reburn. For this purpose, it is necessary to extend the well-known four-step flame-chemistry description to six steps, with acetylene taken out of steady-state and one-step production of nitric oxide included. Emission indices are calculated as functions of the rate of scalar dissipation at the stoichiometric mixture fraction for near-atmospheric pressures and shown to be in reasonable agreement with results obtained from numerical integrations. The various mechanisms of NO{sub x} production and consumption are verified to be strongly dependent on the flame temperature and on superequilibrium concentrations of radicals, both fuel-derived and from hydrogen-oxygen chemistry; the flame-structure analysis was extended to provide sufficient accuracy in the prediction of these quantities. It was found that for flames in near-normal ambient atmospheres, the prompt mechanism usually is most important. For longer residence times, and especially for ambient pressures and temperatures above standard, the thermal mechanism was found to increase in importance, but this increase was calculated to be offset almost entirely by NO consumption through reburn reactions. Conditions that favor reburn were observed to be those where the ratio of radical concentrations to NO concentrations is small. Longer residence times and higher pressures were demonstrated to lead both to more complete heat release and to smaller superequilibrium radical concentrations whence the correspondence between thermal production and reburn. The nitrous oxide mechanism was found to be generally less important for the conditions considered here.

  7. Contribution to the understanding of the ZrNb(l%)O(0.13%) oxidation mechanism at 500 °C in dry air

    NASA Astrophysics Data System (ADS)

    Vermoyal, J. J.; Frichet, A.; Dessemond, L.

    2004-06-01

    The oxidation of ZrNb(l%)O(0.13%) at 500 °C in dry air was investigated in situ by thermogravimetric analyses and electrochemical impedance spectroscopy. Sheets of the alloy were coated with different noble metals (Pt, Au, Ag) as electrode material. After an initial sub-parabolic rate law, the kinetics of ZrNb(l%)O(0.13%) oxidation are characterized by a transition to another decreasing rate law for different times and thicknesses. Noble metals were observed to clearly modify the oxidation rate, even when a pre-oxidized zirconia film was formed before the deposit and the increase in the oxidation rate was always monitored for thick oxides (30 μm). The kinetic transition is hypothesized to be associated with the microstructural degradation of the oxide film. Localized oxidation rate increases were revealed by scanning electron microscopy at the tip of radial cracks distributed on more than 2% of the total area of the sample. Catalytic effects observed on the oxidation rate after the noble metal deposition suggest that the mechanism controlling the oxidation rate is not a solely one of oxygen diffusion through the oxide layer. The reaction of oxygen reduction at the oxide/metal/gas interface partially controls the oxidation kinetics of ZrNb(l%)O(0.13%). Complex electrical signatures monitored during the oxide growth corroborate this assumption and hence indicate that oxygen reduction is still partially controlling the oxidation rate when noble metal are present on ZrNb(l%)O(0.13%) surface. Finally, a mixed process of interfacial-diffusion mechanism is proposed to be the rate determining step for ZrNb(l%)O(0.13%) oxidation in this environment.

  8. Assessment of potato losses caused by oxidant air pollution in New Jersey

    SciTech Connect

    Clarke, B.B.; Henninger, M.R.; Brennan, E.

    1983-01-01

    During 1978 and 1980, three potato cultivars were grown in the field and harvested according to standard commercial practices. A drench of EDU, (N-(2-((oxo-1-imidazolidinyl)ethyl)N'-phenylurea), an antioxidant, was applied to one-half the plants to protect against oxidant injury. The order of foliar sensitivity of these cultivars to oxidant was Norland > Norchip > Green Mountain. Generally, foliar injury was a function of the cumulative oxidant dose, and the time of maximum plant susceptibility was cultivar-dependent. When over 60% of the foliage was injured, tuber yield was reduced 25 and 31% in plants of cultivars Norland and Norchip, respectively. Yield reduction was traced to smaller sized potatoes in the Norland cultivar and to fewer tubers in the Norchip cultivar. The specific gravity of Norland tubers was significantly reduced in both years. When the two cultivars showed equally severe foliar injury, tuber yield of Norchip showed a greater reduction than Norland. 18 references, 3 figures, 3 tables.

  9. Cyclic Oxidation of Ti-48%Al-2%Cr-2%Nb-(0~1%)W Alloys Between 800 and 1000°C in Air

    NASA Astrophysics Data System (ADS)

    Bak, Sang-Hwan; Seo, Dong Yi; Kim, Seon-Jin; Lee, Jae Chun; Lee, Dong Bok

    Ti-48%Al-2%Cr-2%Nb-(0, 0.5, 1) at.%W alloys were synthesized via the powder metallurgical route, and cyclically oxidized at 800, 900, or 1000°C in air for up to 100 h in order to find the effects of W on their oxidation characteristics. At 800°C, they oxidized relatively slowly, and the scales were thin and adherent. At 900°C, the scales began to spall locally. At 1000°C, they spalled repetitively during oxidation. Cr, Nb, and W improved the cyclic oxidation resistance of TiAl alloys. The oxides formed were TiO2 and Al2O3, which contained the alloying elements of Cr, Nb, and W. Nitrides formed were TiN and Ti2AlN.

  10. [The modelling of the composition of the thermal oxidative breakdown products of aviation oils determined in the cabin air of aircraft].

    PubMed

    Belkin, B I; Filippov, A F; Kozlovskaia, N N

    1994-01-01

    The authors suggested a method to obtain a mixture of chemicals from splitting thermo-oxidation of aviation oil. The qualitative and quantitative aspects of the mixture correspond to the concentration of the chemicals in the air of aircraft cabins. The possibility to obtain such mixtures helps to assess in hygienic laboratory conditions a level of air pollution with aviation oil in aircraft cabins. PMID:7834229

  11. Association between changes in exposure to air pollution and biomarkers of oxidative stress in children before and during the Beijing Olympics.

    PubMed

    Lin, Weiwei; Zhu, Tong; Xue, Tao; Peng, Wei; Brunekreef, Bert; Gehring, Ulrike; Huang, Wei; Hu, Min; Zhang, Yuanhang; Tang, Xiaoyan

    2015-04-15

    It is not known whether exposure to air pollutants causes systemic oxidative stress in children. We investigated the association between exposure to air pollution and biomarkers of oxidative stress in relation to a governmental air quality intervention implemented during the 2008 Beijing Olympic Games. We studied 36 schoolchildren during 5 time periods before and during the Olympic Games in Beijing (June 2007-September 2008). The oxidative stress biomarkers 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG) and malondialdehyde were measured in urine samples collected daily during each period. Generalized estimating equations were used to examine the relationship between repeated biomarker measurements and ambient air pollutant levels. During the Olympic intervention period, substantial reductions in air pollution (-19% to -72%), urinary 8-oxodG concentrations (-37.4%; 95% confidence interval: -53.5, -15.7), and urinary malondialdehyde concentrations (-25.3%; 95% confidence interval: -34.3, -15.1) were found. Malondialdehyde and 8-oxodG were significantly associated with concentrations of black carbon, fine particulate matter with an aerodynamic with diameter less than 2.5 μm, sulfur dioxide, nitrogen dioxide, and carbon monoxide. Biomarker changes per each interquartile-range increase in pollutants were largest at lag 0 or lag 1. In a 2-pollutant model, the most robust associations were for black carbon. These findings suggest that exposure to black carbon leads to systemic oxidative stress in children. PMID:25770981

  12. Air/surface exchange of nitric oxide between two typical vegetable lands and the atmosphere in the Yangtze Delta, China

    NASA Astrophysics Data System (ADS)

    Fang, Shuangxi; Mu, Yujing

    Few researches had been carried out so far to study Air/surface exchange of nitric oxide between vegetable lands and the atmosphere. In this study, NO fluxes from two kinds of widely cultivated vegetable fields in the Yangtze Delta, China were measured with static chamber method. The average NO fluxes were 11.5 and 34.2 ng N m -2 s -1 for cabbage (CA) and potato (PO) fields, respectively. The volatile NO sbnd N from the applied fertilizer approximately amounted to 0.6% and 3.6% for CA and PO fields, respectively. The total amount of NO emitted from the vegetable lands in this area during the investigated period was roughly estimated to be 9.1 Gg N, which accounted for about 6.5% of the total emissions from uplands in China. These results indicated that the vegetable fields acted as an important source of atmospheric NO in this area.

  13. Pd@Cu(II)-MOF-Catalyzed Aerobic Oxidation of Benzylic Alcohols in Air with High Conversion and Selectivity.

    PubMed

    Chen, Gong-Jun; Wang, Jing-Si; Jin, Fa-Zheng; Liu, Ming-Yang; Zhao, Chao-Wei; Li, Yan-An; Dong, Yu-Bin

    2016-03-21

    A new 3D porous Cu(II)-MOF (1) was synthesized based on a ditopic pyridyl substituted diketonate ligand and Cu(OAc)2 in solution, and it features a 3D NbO motif which is determined by the X-ray crystallography. Furthermore, the Pd NPs-loaded hybrid material Pd@Cu(II)-MOF (2) was prepared based on 1 via solution impregnation, and its structure was confirmed by HRTEM, SEM, XRPD, gas adsorption-desorption, and ICP measurement. 2 exhibits excellent catalytic activity (conversion, 93% to >99%) and selectivity (>99% to benzaldehydes) for various benzyl alcohol substrates (benzyl alcohol and its derivatives with electron-withdrawing and electron-donating groups) oxidation reactions in air. In addition, 2 is a typical heterogeneous catalyst, which was confirmed by hot solution leaching experiment, and it can be recycled at least six times without significant loss of its catalytic activity and selectivity. PMID:26959340

  14. Numerical Modeling of Oxidized 2D C/SiC Composites in Air Environments Below 900 °C: Microstructure and Elastic Properties

    NASA Astrophysics Data System (ADS)

    Sun, Zhigang; Chen, Xihui; Shao, Hongyan; Song, Yingdong

    2016-08-01

    A numerical model is presented for simulation of the oxidation-affected behaviors of two dimensional carbon fiber-reinforced silcon carbide matrix composite (2D C/SiC) exposed to air oxidizing environments below 900 °C, which incorporates the modeling of oxidized microstructure and computing of degraded elastic properties. This model is based upon the analysis of the representative volume cell (RVC) of the composite. The multi-scale model of 2D C/SiC composites is concerned in the present study. Analysis results of such a composite can provide a guideline for the real 2D C/SiC composite. The micro-structure during oxidation process is firstly modeled in the RVC. The elastic moduli of oxidized composite under non-stress oxidation environment is computed by finite element analysis. The elastic properties of 2D-C/SiC composites in air oxidizing environment are evaluated and validated in comparison to experimental data. The oxidation time, temperature and fiber volume fractions of C/SiC composite are investigated to show their influences upon the elastic properties of 2D C/SiC composites.

  15. Numerical Modeling of Oxidized 2D C/SiC Composites in Air Environments Below 900 °C: Microstructure and Elastic Properties

    NASA Astrophysics Data System (ADS)

    Sun, Zhigang; Chen, Xihui; Shao, Hongyan; Song, Yingdong

    2016-04-01

    A numerical model is presented for simulation of the oxidation-affected behaviors of two dimensional carbon fiber-reinforced silcon carbide matrix composite (2D C/SiC) exposed to air oxidizing environments below 900 °C, which incorporates the modeling of oxidized microstructure and computing of degraded elastic properties. This model is based upon the analysis of the representative volume cell (RVC) of the composite. The multi-scale model of 2D C/SiC composites is concerned in the present study. Analysis results of such a composite can provide a guideline for the real 2D C/SiC composite. The micro-structure during oxidation process is firstly modeled in the RVC. The elastic moduli of oxidized composite under non-stress oxidation environment is computed by finite element analysis. The elastic properties of 2D-C/SiC composites in air oxidizing environment are evaluated and validated in comparison to experimental data. The oxidation time, temperature and fiber volume fractions of C/SiC composite are investigated to show their influences upon the elastic properties of 2D C/SiC composites.

  16. Plasma-surface modification vs air oxidation on carbon obtained from peach stone: Textural and chemical changes and the efficiency as adsorbents

    NASA Astrophysics Data System (ADS)

    De Velasco Maldonado, Paola S.; Hernández-Montoya, Virginia; Montes-Morán, Miguel A.

    2016-10-01

    Carbons were prepared from peach stones (Prunus persica) using different carbonization temperatures (600, 800 and 1000 °C). A selected sample was modified by oxidation using conventional oxidation techniques (thermal treatment in air atmosphere) and with cold oxygen plasma oxidation, under different conditions. Samples were characterized using elemental analysis, FT-IR spectroscopy, nitrogen adsorption isotherms at -196 °C, SEM/EDX analysis, potentiometric titration and XPS analysis. Carbons with and without oxidation were employed in the adsorption of Pb2+ in aqueous solution. Results obtained indicated that the materials with high contents of acidic oxygen groups were more efficient in the removal of Pb2+, values as high as approx. 40 mg g-1 being obtained for the best performing carbon. Textural properties of the original, un-oxidized carbon were significantly altered only after oxidation under air atmosphere at 450 °C. On the other hand, the samples oxidized with plasma show little changes in the textural parameters and a slight increase in the specific surface was observed for the sample treated at high RF power (100 W). Additionally, a significant increment of the oxygen content was observed for the plasma oxidized samples, as measured by XPS.

  17. Oxidative DNA damage estimated by urinary 8-hydroxydeoxyguanosine and indoor air pollution among non-smoking office employees.

    PubMed

    Lu, Chung-Yen; Ma, Yee-Chung; Lin, Jia-Min; Chuang, Chun-Yu; Sung, Fung-Chang

    2007-03-01

    This study investigated whether urinary 8-hydroxydeoxyguanosine (8-OHdG), a biomarker of oxidative stress, was associated with indoor air quality for non-smokers in high-rise building offices. With informed consents, urine samples from 344 non-smoking employees in 86 offices were collected to determine 8-OHdG concentrations. The concentrations of carbon dioxide (CO(2)) and total volatile organic compounds (TVOCs) in each office and outside of the building were simultaneously measured for eight office hours. The average workday difference between indoor and outdoor CO(2) concentrations (dCO(2)) was used as a surrogate measure of the ventilation efficiency for each office unit. The CO(2) levels in the offices ranged 467-2810ppm with a mean of 1170ppm, or 2.7 times higher than that in the outside air. The average urinary 8-OHdG levels among employees increased from 3.10 micro g/g creatinine, for those at the lowest tertile levels of both dCO(2) and TVOCs, to 6.27 micro g/g creatinine, for those at the highest tertile levels. Multivariate logistic regression analysis showed that the risk of having the urinary 8-OHdG level of greater than the median, 4.53 micro g/g creatinine, for participants was increased significantly at the highest tertile dCO(2) level of >680ppm (odds ratio (OR)=3.37, 95% confidence interval (CI)=1.20-9.46). The effect was significant at the middle tertile TVOCs level of 114-360ppb (OR=2.62, 95% CI=1.43-4.79), but not at the highest tertile. Inadequate ventilation in office increases the risk of building-related oxidative stress in non-smoking employees. PMID:17034784

  18. Oxidative Stress and Systemic Inflammation as Modifiers of Cardiac Autonomic Responses to Particulate Air Pollution

    PubMed Central

    Lee, Mi-Sun; Eum, Ki-Do; Fang, Shona C.; Rodrigues, Ema G.; Modest, Geoffrey A.; Christiani, David C.

    2014-01-01

    Background The role of oxidative stress and systemic inflammation on the association between personal exposures to ambient fine particulate matter ≤ 2.5 μm in diameter (PM2.5) and cardiac autonomic dysfunction, indicated by reduction in heart rate variability (HRV), has not been examined. Methods We performed a repeated measures study on community adults in a densely populated inner city neighborhood in Boston, Massachusetts. Continuous ambulatory electrocardiogram (ECG) monitoring and personal exposure to PM2.5 were measured for up to two consecutive days. Peripheral blood and spot urine samples were collected at 12-hour intervals for the measurements of markers of inflammation including C-reactive protein (CRP), fibrinogen, white blood cell (WBC) and platelet counts as well as for the analysis of urinary 8-hydroxy-2′-deoxyguanosine (8-OHdG), a marker of oxidative DNA damage. Results After adjusting for confounders, we found a pronounced decrease in nighttime standard deviation of normal-to normal intervals (SDNN): an interquartile range (IQR) increase in PM2.5 (13.6 μg/m3) was associated with an 8.4% decrease in SDNN (95% CI: −11.3 to −5.5). Compared with the lower eightieth percentile, significantly greater PM2.5 associated nighttime SDNN reductions were observed among subjects in the upper twentieth percentile of 8-OHdG by −25.3%, CRP by −24.9%, fibrinogen by −28.7%, WBC by −23.4%, and platelet counts by −24.0% (all P < 0.0001; all Pinteraction <0.01). Conclusions These data suggest that oxidative stress and systemic inflammation exacerbate the adverse effects of PM2.5 on the cardiac autonomic function even at ambient levels of exposure. PMID:25074558

  19. Final report on the oxidation of energetic materials in supercritical water. Final Air Force report

    SciTech Connect

    Buelow, S.J.; Allen, D.; Anderson, G.K.

    1995-04-03

    The objective of this project was to determine the suitability of oxidation in supercritical fluids (SCO), particularly water (SCWO), for disposal of propellants, explosives, and pyrotechnics (PEPs). The SCO studies of PEPs addressed the following issues: The efficiency of destruction of the substrate. The products of destruction contained in the effluents. Whether the process can be conducted safely on a large scale. Whether energy recovery from the process is economically practicable. The information essential for process development and equipment design was also investigated, including issues such as practical throughput of explosives through a SCWO reactor, reactor materials and corrosion, and models for process design and optimization.

  20. Band gap shift in the indium-tin-oxide films on polyethylene napthalate after thermal annealing in air

    NASA Astrophysics Data System (ADS)

    Han, H.; Mayer, J. W.; Alford, T. L.

    2006-10-01

    Indium-tin-oxide (ITO) thin films on polyethylene napthalate (PEN) with high carrier concentration (˜1021/cm3) have been grown by electron-beam deposition without the introduction of oxygen into the chamber. The electrical properties of the ITO films (such as, carrier concentration, electrical mobility, and resistivity) abruptly changed after annealing in the air atmospheres. In addition, optical transmittance and optical band gap values significantly changed after heat treatment. The optical band gap narrowing behavior is observed in the as-deposited sample because of impurity band and heavy carrier concentration. The influence of annealing in air on the electrical and optical properties of ITO/PEN samples can be explained by the change in the free electron concentration, which is evaluated in terms of the oxygen content. Rutherford backscattering spectrometry and x-ray photoelectron spectroscopy analyses are used to determine the oxygen content in the film. Hall effect measurements are used to determine the dependence of electrical properties on oxygen content.

  1. Polystyrene-poly(ethylene oxide) diblock copolymer: the effect of polystyrene and spreading concentration at the air/water interface.

    PubMed

    Glagola, Cameron P; Miceli, Lia M; Milchak, Marissa A; Halle, Emily H; Logan, Jennifer L

    2012-03-20

    Polystyrene-block-poly(ethylene oxide) (PS-PEO) is an amphiphilic diblock copolymer that undergoes microphase separation when spread at the air/water interface, forming nanosized domains. In this study, we investigate the impact of PS by examining a series of PS-PEO samples containing constant PEO (~17,000 g·mol(-1)) and variable PS (from 3600 to 200,000 g·mol(-1)) through isothermal characterization and atomic force microscopy (AFM). The polymers separated into two categories: predominantly hydrophobic and predominantly hydrophilic with a weight percent of PEO of ~20% providing the boundary between the two. AFM results indicated that predominantly hydrophilic PS-PEO forms dots while more hydrophobic samples yield a mixture of dots and spaghetti with continent-like structures appearing at ~7% PEO or less. These structures reflect a blend of polymer spreading, entanglement, and vitrification as the solvent evaporates. Changing the spreading concentration provides insight into this process with higher concentrations representing earlier kinetic stages and lower concentrations demonstrating later ones. Comparison of isothermal results and AFM analysis shows how polymer behavior at the air/water interface correlates with the observed nanostructures. Understanding the impact of polymer composition and spreading concentration is significant in leading to greater control over the nanostructures obtained through PS-PEO self-assembly and their eventual application as polymer templates. PMID:22339480

  2. Preliminary study on zinc-air battery using zinc regeneration electrolysis with propanol oxidation as a counter electrode reaction

    NASA Astrophysics Data System (ADS)

    Wen, Yue-Hua; Cheng, Jie; Ning, Shang-Qi; Yang, Yu-Sheng

    A zinc-air battery using zinc regeneration electrolysis with propanol oxidation as a counter electrode reaction is reported in this paper. It possesses functions of both zincate reduction and electrochemical preparation, showing the potential for increasing the electronic energy utilization. Charge/discharge tests and scanning electron microscopy (SEM) micrographs reveal that when a nickel sheet plated with the high-H 2-overpotential metal, cadmium, was used as the negative substrate electrode, the dendritic formation and hydrogen evolution are suppressed effectively, and granular zinc deposits become larger but relatively dense with the increase of charge time. The performance of batteries is favorable even if the charge time is as long as 5 h at the current density of 20 mA cm -2. Better discharge performance is achieved using a 'cavity-opening' configuration for the discharge cell rather than a 'gas-introducing' configuration. The highest energy efficiency is up to 59.2%. That is, the energy consumed by organic electro-synthesis can be recovered by 59.2%. Cyclic voltammograms show that the sintered nickel electrode exhibits a good electro-catalysis activity for the propanol oxidation. The increase of propanol concentration conduces to an enhancement in the organic electro-synthesis efficiency. The organic electro-synthesis current efficiency of 82% can be obtained.

  3. Steam Methane Reformation Testing for Air-Independent Solid Oxide Fuel Cell Systems

    NASA Technical Reports Server (NTRS)

    Mwara, Kamwana N.

    2015-01-01

    Recently, NASA has been looking into utilizing landers that can be propelled by LOX-CH (sub 4), to be used for long duration missions. Using landers that utilize such propellants, also provides the opportunity to use solid oxide fuel cells as a power option, especially since they are able to process methane into a reactant through fuel reformation. One type of reformation, called steam methane reformation, is a process to reform methane into a hydrogen-rich product by reacting methane and steam (fuel cell exhaust) over a catalyst. A steam methane reformation system could potentially use the fuel cell's own exhaust to create a reactant stream that is hydrogen-rich, and requires less internal reforming of the incoming methane. Also, steam reformation may hold some advantages over other types of reforming, such as partial oxidation (PROX) reformation. Steam reformation does not require oxygen, while up to 25 percent can be lost in PROX reformation due to unusable CO (sub 2) reformation. NASA's Johnson Space Center has conducted various phases of steam methane reformation testing, as a viable solution for in-space reformation. This has included using two different types of catalysts, developing a custom reformer, and optimizing the test system to find the optimal performance parameters and operating conditions.

  4. Influences of flame-vortex interactions on formation of oxides of nitrogen in curved methane-air diffusion flamelets

    SciTech Connect

    Card, J.M.; Ryden, R.; Williams, F.A.

    1994-01-01

    To improve knowledge of production rates of nitrogen oxides in turbulent diffusion flames in reaction-sheet regimes, an analytical investigation is made of the structure of a parabolic flamelet. The mixture-fraction field, scalar dissipation rate and gas velocity relative to the flamelet in the vortex are related to flame curvature at the parabolic tip. Flame structure for major species and temperature is described by rate-ratio asymptotics based on two-step and three-step reduced chemical-kinetic mechanisms. Production rates by prompt, thermal and nitrous-oxide mechanisms are obtained from one-step reduced-chemistry approximations that employ steady states for all reaction intermediaries. For sufficiently large streamwise separation distances between isoscalar surfaces, it is found that equilibrium conditions are closely approached near the flame tip, and the thermal mechanism dominates there, but the prompt mechanism always dominates in the wings, away from the tip, where the highest rates of scalar dissipation occur. Increasing the tip curvature increases the Peclet number and the prompt contribution while decreasing the thermal contribution. At 1 atm and ambient temperatures of 300 K, the prompt mechanism always dominates the total production rate in the parabolic flamelet, and, perhaps surprisingly, the rate of the nitrous-oxide mechanism is faster than that of the thermal mechanism and varies with the tip curvature and with scalar dissipation in the same manner as that of the prompt mechanism, different from that of the thermal mechanism. Conclusion reached is that Zel`dovich NO is relatively insignificant in hydrocarbon-air mixtures in reaction-sheet regimes.

  5. The effect of fission products on the rate of U3O8 formation in SIMFUEL oxidized in air at 250°C

    NASA Astrophysics Data System (ADS)

    Choi, Jong-Won; McEachern, Rod J.; Taylor, Peter; Wood, Donald D.

    1996-06-01

    The effect of fission products on the rate of U3O8 formation was investigated by oxidizing UO2-based SIMFUEL (simulated high burnup nuclear fuel) and unirradiated UO2 fuel specimens in air at 250°C for different times (1-317 days). The progress of oxidation was monitored by X-ray diffraction, revealing that the rate of U3O8 formation declines with increasing burnup. An expression was derived to describe quantitatively the time for U3O8 powder formation as a function of simulated burnup. These findings were supported by additional isochronal oxidation experiments conducted between 200 and 300°C.

  6. Increased nitric oxide in exhaled air: an early marker of asthma in non-smoking aluminium potroom workers?

    PubMed Central

    Lund, M; Oksne, P; Hamre, R; Kongerud, J

    2000-01-01

    OBJECTIVES—To study exhaled nitric oxide (NO) as a marker of airway inflammation caused by potroom exposure, hypothesising that (a) workers exposed to potroom pollutants would have higher concentrations of NO in expired air than control subjects employed at the same plant but working outside of the potroom atmosphere, and (b) that concentrations of exhaled NO in potroom employees might be positively associated with concentrations of fluoride and exposure to dust.
METHODS—A study group comprising 186 male subjects (aged 24-63 years), employed in the potrooms of one Norwegian aluminium smelter, and 40 comparable control subjects (aged 25-60 years) recruited from the same plant, were examined by measurements of exhaled and nasal concentrations of NO, spirometry, and a questionnaire on respiratory symptoms as a part of an annual health surveillance programme. Estimates of exposure to fluorides and dust for selected job categories were obtained by means of personal samplers carried by the workers.
RESULTS—In the non-smokers, the concentrations of exhaled NO were higher in the potroom workers than in the controls (median (interquartile range) 9.3 (6.2-15.6) v 5.7 (4.6-8.3) ppb, p=0.001). The two groups did not differ in spirometry and asthma-like symptoms. Non-smoking potroom workers with asthma-like symptoms had higher concentrations of exhaled NO than those with no symptoms (median (interquartile range) 21.0 (19.3-41.4) v 8.5 (5.9-12.8) ppb, p=0.001), but had comparable spirometric values. In subjects who smoked, the concentrations of exhaled NO did not differ significantly between potroom workers and controls (median (interquartile range) 4.6 (3.3-8.0) v 4.0 (3.4-5.1) ppb. Exhaled NO was not significantly associated with either duration of employment or routine measurements of dust and fluorides.
CONCLUSIONS—Exposure to potroom pollutants is associated with increased concentrations of exhaled NO in non-smoking subjects. Nitric oxide in exhaled

  7. Oxidative Stress of Office Workers Relevant to Tobacco Smoking and Inner Air Quality

    PubMed Central

    Lu, Chung-Yen; Ma, Yee-Chung; Chen, Pei-Chun; Wu, Chin-Ching; Chen, Yi-Chun

    2014-01-01

    Studies have used 8-hydroxydeoxyguanosine (8-OHdG) as a biomarker to detect systemic oxidative DNA damage associated with oxidative stress. However, studies on the association between exposure to tobacco smoking and urinary 8-OHdgG give inconsistent results. Limited studies have estimated the oxidative stress among office workers. This study assessed the association between urinary 8-OHdG and cotinine for office workers. Workers (389) including smokers, ex-smokers and non-smokers from 87 offices at high-rise buildings in Taipei participated in this study with informed consent. Each participant completed a questionnaire and provided a spot urine specimen at the end of work day for measuring urinary 8-OHdG and cotinine. The carbon dioxide (CO2) levels in workers’ offices were also measured. The questionnaire reported socio-demographic characteristics, life styles and allergic history. The urinary 8-OHdG level increased with the cotinine level among participants (Spearmans’ rho = 0.543, p < 0.001). The mean of urinary 8-OHdG and cotinine was 5.81 ± 3.53 μg/g creatinine and 3.76 ± 4.06 μg/g creatinine, respectively. Comparing with non-smokers, the adjusted odds ratio (OR) of having urinary 8-OHdG greater than the median level of 4.99 μg/g creatinine was 5.30 (95% confidence intervals (CI) = 1.30–21.5) for current smokers and 0.91 (95% CI = 0.34–2.43) for former smokers. We also found workers exposed to 1,000 ppm of CO2 at offices had an adjusted OR of 4.28 (95% CI = 1.12–16.4) to have urinary 8-OHdG greater than 4.99 μg/g creatinine, compared to those exposed to indoor CO2 under 600 ppm. In conclusion, urinary 8-OHdG could represent a suitable marker for measuring smoking and CO2 exposure for office workers. PMID:24865395

  8. Mild and selective vanadium-catalyzed oxidation of benzylic, allylic, and propargylic alcohols using air

    DOEpatents

    Hanson, Susan Kloek; Silks, Louis A; Wu, Ruilian

    2013-08-27

    The invention concerns processes for oxidizing an alcohol to produce a carbonyl compound. The processes comprise contacting the alcohol with (i) a gaseous mixture comprising oxygen; and (ii) an amine compound in the presence of a catalyst, having the formula: ##STR00001## where each of R.sup.1-R.sup.12 are independently H, alkyl, aryl, CF.sub.3, halogen, OR.sup.13, SO.sub.3R.sup.14, C(O)R.sup.15, CONR.sup.16R.sup.17 or CO.sub.2R.sup.18; each of R.sup.13-R.sup.18 is independently alkyl or aryl; and Z is alkl or aryl.

  9. OXIDATIVE STRESS PARTICIPATES IN ACUTE LUNG INJURY AND ACTIVATION OF MITOGEN ACTIVATED PROTEIN KINASES (MAPK) FOLLOWING AIR POLLUTION PARTICLE EXPOSURE (PM)

    EPA Science Inventory

    OXIDATIVE STRESS PARTICIPATES IN ACUTE LUNG INJURY AND ACTIVATION OF MITOGEN ACTIVATED PROTEIN KINASES (MAPK) FOLLOWING AIR POLLUTION PARTICLE EXPOSURE (PM). E S Roberts1, R Jaskot2, J Richards2, and K L Dreher2. 1College of Veterinary Medicine, NC State University, Raleigh, NC a...

  10. Investigation of the impact of imposed air inlet velocity oscillations on the formation and oxidation of soot using simultaneous 2-Colour-TIRE-LII

    NASA Astrophysics Data System (ADS)

    Aleksandrov, A.; Suntz, R.; Bockhorn, H.

    2015-05-01

    The response of non-premixed swirling flames to acoustic perturbations at various frequencies (0-350 Hz) and the impact of imposed air inlet velocity oscillations on the formation and oxidation of soot are investigated. The results obtained from these flames are of special interest for "rich-quenched-lean" (RQL) combustion concepts applied in modern gas turbines. In RQL combustion, the fuel is initially oxidized by air under fuel-rich conditions in a first stage followed by a fuel-lean combustion step in a second stage. To mimic soot formation and oxidation in RQL combustion, soot particle measurements in highly turbulent, non-premixed swirling natural gas/ethylene-confined flames at imposed air inlet velocity oscillations are performed using simultaneous 2-Colour-Time-Resolved-Laser-Induced Incandescence (simultaneous 2-Colour-TIRE-LII). The latter technique is combined with line-of-sight averaged OH*-chemiluminescence imaging, measurements of the velocity field by high-speed particle imaging velocimetry under reactive combustion conditions and measurements of the mean temperature field obtained by a thermocouple. A natural gas/ethylene mixture (Φ = 1.56, 42 % C2H4, 58 % natural gas, P th = 17.6 kW at atmospheric pressure) is used as a fuel, which is oxidized by air under fuel-rich conditions in the first combustion chamber.

  11. Deep Desulfurization of Diesel Fuels with Plasma/Air as Oxidizing Medium, Diperiodatocuprate (III) as Catalyzer and Ionic Liquid as Extraction Solvent

    NASA Astrophysics Data System (ADS)

    Ban, Lili; Liu, Ping; Ma, Cunhua; Dai, Bin

    2013-12-01

    In this paper, the oxidative desulfurization (ODS) system is directly applied to deal with the catalytic oxidation of sulfur compounds of sulfur-containing model oil by dielectric barrier discharge (DBD) plasma in the presence of air plus an extraction step with the oxidation-treated fuel put over ionic liquid [BMIM]FeCl4 (1-butyl-3-methylimidazolium tetrachloroferrate). This new system exhibited an excellent desulfurization effect. The sulfur content of DBT in diesel oil decreased from 200 ppm to 4.92 ppm (S removal rate up to 97.5%) under the following optimal reaction conditions: air flow rate (ν) of 60 mL/min, amplitude of applied voltage (U) on DBD of 16 kV, input frequency (f) of 79 kHz, catalyst amount (ω) of 1.25 wt%, reaction time (t) of 10 min. Moreover, a high desulfurization rate was obtained during oxidation of benzothiophene (BT) or 4,6-DMDBT (4,6-dimethyl-dibenzothiophene) under the aforementioned conditions. The oxidation reactivity of different S compounds was decreased in the order of DBT, 4,6-DMDBT and BT. The remarkable advantage of the novel ODS system is that the desulfurization condition applies in the presence of air at ambient conditions without peroxides, aqueous solvent or biphasic oil-aqueous solution system.

  12. Oxygen reduction and evolution reactions of air electrodes using a perovskite oxide as an electrocatalyst

    NASA Astrophysics Data System (ADS)

    Nishio, Koji; Molla, Sergio; Okugaki, Tomohiko; Nakanishi, Shinji; Nitta, Iwao; Kotani, Yukinari

    2015-03-01

    The oxygen reduction reaction (ORR) and the oxygen evolution reaction (OER) of air electrodes consisting of La0.5Sr0.5CoO3 and/or carbon in the electrocatalyst layer are studied by using two types of gas diffusion electrodes. Cyclic voltammetry and square wave voltammetry studies reveal very low ORR activity of carbon-free perovskite and remarkably enhanced ORR of perovskite-carbon composites. The ORR current density at -0.5 V vs. Hg/HgO is higher than 200 mA cm-2 in a wide range of perovskite-carbon composition, suggesting good peroxide reducing capability of the perovskite. The ORR mechanisms of perovskite-carbon composites are consistent with the 2+2-electron mechanisms. The ORR and OER properties of perovskite-carbon composite electrodes are significantly influenced by the carbon species. The electrode exhibits a higher ORR current density, but inferior cycling performances when a carbon material with a higher specific surface area is used, and vice versa. Under a current density of 20 mA cm-2 and ORR and OER durations of 30 min, a gas diffusion type electrode consists of La0.5Sr0.5CoO3 and a low surface area carbon are capable of more than 150 cycles.

  13. Dairy Biomass-Wyoming Coal Blends Fixed Gasification Using Air-Steam for Partial Oxidation

    DOE PAGESBeta

    Gordillo, Gerardo; Annamalai, Kalyan

    2012-01-01

    Concenmore » trated animal feeding operations such as dairies produce a large amount of manure, termed as dairy biomass (DB), which could serve as renewable feedstock for thermal gasification. DB is a low-quality fuel compared to fossil fuels, and hence the product gases have lower heat content; however, the quality of gases can be improved by blending with coals. This paper deals with air-steam fixed-bed counterflow gasification of dairy biomass-Wyoming coal blend (DBWC). The effects of equivalence ratio ( 1.6 < Φ < 6.4 ) and steam-to-fuel ratio ( 0.4 < S : F < 0.8 ) on peak temperatures, gas composition, gross heating value of the products, and energy recovery are presented. According to experimental results, increasing Φ and ( S : F ) ratios decreases the peak temperature and increases the H 2 and CO 2 production, while CO production decreases. On the other hand, the concentrations of CH 4 and C 2 H 6 were lower compared to those of other gases and almost not affected by Φ.« less

  14. Particulate air pollution induces arrhythmia via oxidative stress and calcium calmodulin kinase II activation

    SciTech Connect

    Kim, Jin-Bae; Kim, Changsoo; Choi, Eunmi; Park, Sanghoon; Park, Hyelim; Pak, Hui-Nam; Lee, Moon-Hyoung; Shin, Dong Chun; Hwang, Ki-Chul; Joung, Boyoung

    2012-02-15

    Ambient particulate matter (PM) can increase the incidence of arrhythmia. However, the arrhythmogenic mechanism of PM is poorly understood. This study investigated the arrhythmogenic mechanism of PM. In Sprague–Dawley rats, QT interval was increased from 115.0 ± 14.0 to 142.1 ± 18.4 ms (p = 0.02) after endotracheal exposure of DEP (200 μg/ml for 30 min, n = 5). Ventricular premature contractions were more frequently observed after DEP exposure (100%) than baseline (20%, p = 0.04). These effects were prevented by pretreatment of N-acetylcysteine (NAC, 5 mmol/L, n = 3). In 12 Langendorff-perfused rat hearts, DEP infusion of 12.5 μg/ml for 20 min prolonged action potential duration (APD) at only left ventricular base increasing apicobasal repolarization gradients. Spontaneous early afterdepolarization (EAD) and ventricular tachycardia (VT) were observed in 8 (67%) and 6 (50%) hearts, respectively, versus no spontaneous triggered activity or VT in any hearts before DEP infusion. DEP-induced APD prolongation, EAD and VT were successfully prevented with NAC (5 mmol/L, n = 5), nifedipine (10 μmol/L, n = 5), and active Ca{sup 2+}/calmodulin-dependent protein kinase II (CaMKII) blockade, KN 93 (1 μmol/L, n = 5), but not by thapsigargin (200 nmol/L) plus ryanodine (10 μmol/L, n = 5) and inactive CaMKII blockade, KN 92 (1 μmol/L, n = 5). In neonatal rat cardiomyocytes, DEP provoked ROS generation in dose dependant manner. DEP (12.5 μg/ml) induced apoptosis, and this effect was prevented by NAC and KN 93. Thus, this study shows that in vivo and vitro exposure of PM induced APD prolongation, EAD and ventricular arrhythmia. These effects might be caused by oxidative stress and CaMKII activation. -- Highlights: ► The ambient PM consistently prolonged repolarization. ► The ambient PM induced triggered activity and ventricular arrhythmia. ► These effects were prevented by antioxidants, I{sub CaL} blockade and CaMKII blockade. ► The ambient PM can induce

  15. Research on oxidation by air and tempering of Raney nickel electrocatalysts for the H2 anodes of alkali combustion materials cells. Thesis - Braunschweig Technische Univ., 1982

    NASA Technical Reports Server (NTRS)

    Selbach, H. J.

    1984-01-01

    The controlled oxidation in air of Raney nickel electrocatalysts was studied, with special attention paid to the quantitative analysis of nickel hydroxide. The content of the latter was determined through X-ray studies, thermogravimetric measurements, and spectral photometric examinations. The dependence of the content on the drying of activated catalyst is determined. The influence of nickel hydroxide on the electrochemical parameters of the catalyst, such as diffusion polarization, is studied, including a measurement of the exchange current density using the potential drop method. Conservation by oxidation in air with ancillary stabilization of the oxide in an H2 flow at 300 C is explored, including reduction by H2, the influence of tempering time, and structural studies on conserved and stabilized catalyst, long term research on the catalyst, including the influence of aging on the reduced catalyst, and the results of impedance measurements are presented.

  16. Air-Independent Solid Oxide Fuel Cells for NASA's LOX-CH4 Landers

    NASA Technical Reports Server (NTRS)

    Ryan, Abigail C.; Araghi, Koorosh R.; Farmer, Serene C.

    2013-01-01

    Gemini, Apollo, and Space Shuttle used fuel cells as main power source for vehicle and water source for life support and thermal PEM (Gemini) and Alkaline (Apollo, Shuttle) fuel cells were used Ideal for short (less than 3 weeks) missions when the required O2 and H2 can be launched with the vehicle. New missions that might require long-duration stays in orbit or at a habitat, cannot rely on the availability of pure reactants but should also aim to be sun-independent - a problem for which Solid Oxide Fuel Cells might be the answer. Recently, NASA has investigated & developed LOX/CH4-propelled landers (Altair, MORPHEUS). In order to preserve mission flexibility, fuel cells are being studied as a potential power source. Much of NASA's fuel cell development has been focused on creating a dead-headed, non-flow through PEM fuel cells which would weigh less and be more reliable than the existing Alkaline and PEM technology; however, LOX/CH4 as a propellant introduces SOFCs as a power option due to their ability to accept those reactants without much reforming.

  17. Investigation into the optoelectrical properties of tungsten oxide thin films annealed in an oxygen air

    SciTech Connect

    Arfaoui, A.; Ouni, B. Touihri, S.; Mannoubi, T.

    2014-12-15

    Tungsten oxide (WO{sub x}) thin film have been deposited onto glass substrates using the thermal vacuum evaporation technique, monitored by an annealing process in a variable oxygen atmosphere. Analysis by X-ray diffraction and Raman spectroscopy showed the structural changes from orthorhombic to monoclinic which depend on the annealing temperature and the oxygen content. AFM study shows that the increase of oxygen content leads to a decrease of the root-mean-square from 94.64 nm to 2 nm. Ellipsometric measurements have been used to evaluate the optical constants. Further, it is found that when the oxygen content increases, the band gap of the annealed layer varies from 3.01 eV to 3.52 eV by against, the Urbach energy decreases. The AC conductivity plot showed a universal power law according to the Jonscher model. Moreover, at high frequency semiconductor-to-metallic behavior has been observed. Finally, the effect of annealing in oxygen atmosphere on their structural modifications, morphological, optical properties and electrical conductivity are reported.

  18. Formation of formaldehyde and peroxides by air oxidation of high purity polyoxyethylene surfactants.

    PubMed

    Bergh, M; Magnusson, K; Nilsson, J L; Karlberg, A T

    1998-07-01

    Ethoxylated alcohols are non-ionic surfactants. The majority are used in household cleaners, laundry products, toiletries and in industrial and institutional cleaners. In previous studies, an ethoxylated non-ionic surfactant of technical quality showed allergenic activity in guinea pig experiments. Chemical analysis revealed a content of formaldehyde, a well-known contact allergen, and peroxides in the surfactant. Most cases of occupational contact dermatitis are considered to be of irritant origin, caused by contact with water and surfactants, but if allergenic autoxidation products can be formed, allergic contact dermatitis cannot be excluded. The sensitizing potential of a chemically defined high purity ethoxylated alcohol was investigated and oxidation under various storage and handling conditions was studied for this and a homologous product. The pure surfactant showed no significant allergenic activity on predictive testing in guinea pigs. When ethoxylated alcohols were stored in the refrigerator, their deterioration was limited. At room temperature, their content of peroxides and formaldehyde increased with time. Levels of formaldehyde above those capable of causing positive patch test reactions were found. Since such surfactants have wide applications, resulting exposure to formaldehyde could be more frequent than is generally realized, contributing to persistence of dermatitis in individuals allergic to formaldehyde. PMID:9686972

  19. Health Effects of a Mixture of Indoor Air Volatile Organics, Their Ozone Oxidation Products, and Stress

    PubMed Central

    Fiedler, Nancy; Laumbach, Robert; Kelly-McNeil, Kathie; Lioy, Paul; Fan, Zhi-Hua; Zhang, Junfeng; Ottenweller, John; Ohman-Strickland, Pamela; Kipen, Howard

    2005-01-01

    In our present study we tested the health effects among women of controlled exposures to volatile organic compounds (VOCs), with and without ozone (O3), and psychological stress. Each subject was exposed to the following three conditions at 1-week intervals (within-subject factor): VOCs (26 mg/m3), VOCs + O3 (26 mg/m3 + 40 ppb), and ambient air with a 1-min spike of VOCs (2.5 mg/m3). As a between-subjects factor, half the subjects were randomly assigned to perform a stressor. Subjects were 130 healthy women (mean age, 27.2 years; mean education, 15.2 years). Health effects measured before, during, and after each 140-min exposure included symptoms, neurobehavioral performance, salivary cortisol, and lung function. Mixing VOCs with O3 was shown to produce irritating compounds including aldehydes, hydrogen peroxide, organic acids, secondary organic aerosols, and ultrafine particles (particulate matter with aerodynamic diameter < 0.1 μm). Exposure to VOCs with and without O3 did not result in significant subjective or objective health effects. Psychological stress significantly increased salivary cortisol and symptoms of anxiety regardless of exposure condition. Neither lung function nor neurobehavioral performance was compromised by exposure to VOCs or VOCs + O3. Although numerous epidemiologic studies suggest that symptoms are significantly increased among workers in buildings with poor ventilation and mixtures of VOCs, our acute exposure study was not consistent with these epidemiologic findings. Stress appears to be a more significant factor than chemical exposures in affecting some of the health end points measured in our present study. PMID:16263509

  20. Metal-free porphyrin-sensitized mesoporous titania films for visible-light indoor air oxidation.

    PubMed

    Ismail, Adel A; Bahnemann, Detlef W

    2010-09-24

    Transparent cubic mesoporous TiO2 films coated on soda-lime glass have been developed. A metal free meso-tetrakis(4-sulfonatophenyl) porphyrin (TPPS) has been adsorbed on these TiO2 films from aqueous solutions. The results indicated that the obtained mesoporous TiO2 and 3D TPPS/TiO2 films are optically transparent and crack free (thickness ca. 200±20 nm). The introduction of the TPPS molecules has only a very small influence on the pore system and some limited pore blocking seems to occur. Transmission electron microscopy (TEM) images revealed that the adsorption of TPPS does not disrupt the meso order of TPPS/TiO2. The particle size of these TiO2 nanocrystals has been measured to be approximately 5-8 nm. TPPS/TiO2 photocatalysts, exhibiting regularly ordered mesopores, large surface area (ca. 102.5 cm(2) cm(-2)), and specific pore volume of about 0.1 mm(3) cm(-2), show improved light-harvesting efficiency as compared with other transparent TiO2 films. Employing the 3D TPPS/TiO2 photocatalyst, a quantum efficiency of 0.059 % has been obtained for the photodegradation of CH3CHO in the gas phase under visible-light illumination. Recycling tests demonstrated that the newly synthesized photocatalyst was quite stable during this gas-solid heterogeneous photocatalytic process because no significant decrease in photocatalytic activity was observed even after being used repetitively up to five times. Therefore, the newly synthesized transparent 3D TPPS/TiO2 photocatalysts can potentially be applied for low-cost air purification and self-cleaning applications. PMID:20806316

  1. Induction of Inducible Nitric Oxide Synthase by Lipopolysaccharide and the Influences of Cell Volume Changes, Stress Hormones and Oxidative Stress on Nitric Oxide Efflux from the Perfused Liver of Air-Breathing Catfish, Heteropneustes fossilis.

    PubMed

    Choudhury, Mahua G; Saha, Nirmalendu

    2016-01-01

    The air-breathing singhi catfish (Heteropneustes fossilis) is frequently being challenged by bacterial contaminants, and different environmental insults like osmotic, hyper-ammonia, dehydration and oxidative stresses in its natural habitats throughout the year. The main objectives of the present investigation were to determine (a) the possible induction of inducible nitric oxide synthase (iNOS) gene with enhanced production of nitric oxide (NO) by intra-peritoneal injection of lipopolysaccharide (LPS) (a bacterial endotoxin), and (b) to determine the effects of hepatic cell volume changes due to anisotonicity or by infusion of certain metabolites, stress hormones and by induction of oxidative stress on production of NO from the iNOS-induced perfused liver of singhi catfish. Intra-peritoneal injection of LPS led to induction of iNOS gene and localized tissue specific expression of iNOS enzyme with more production and accumulation of NO in different tissues of singhi catfish. Further, changes of hydration status/cell volume, caused either by anisotonicity or by infusion of certain metabolites such as glutamine plus glycine and adenosine, affected the NO production from the perfused liver of iNOS-induced singhi catfish. In general, increase of hydration status/cell swelling due to hypotonicity caused decrease, and decrease of hydration status/cell shrinkage due to hypertonicity caused increase of NO efflux from the perfused liver, thus suggesting that changes in hydration status/cell volume of hepatic cells serve as a potent modulator for regulating the NO production. Significant increase of NO efflux from the perfused liver was also observed while infusing the liver with stress hormones like epinephrine and norepinephrine, accompanied with decrease of hydration status/cell volume of hepatic cells. Further, oxidative stress, caused due to infusion of t-butyl hydroperoxide and hydrogen peroxide separately, in the perfused liver of singhi catfish, resulted in

  2. Induction of Inducible Nitric Oxide Synthase by Lipopolysaccharide and the Influences of Cell Volume Changes, Stress Hormones and Oxidative Stress on Nitric Oxide Efflux from the Perfused Liver of Air-Breathing Catfish, Heteropneustes fossilis

    PubMed Central

    Choudhury, Mahua G.; Saha, Nirmalendu

    2016-01-01

    The air-breathing singhi catfish (Heteropneustes fossilis) is frequently being challenged by bacterial contaminants, and different environmental insults like osmotic, hyper-ammonia, dehydration and oxidative stresses in its natural habitats throughout the year. The main objectives of the present investigation were to determine (a) the possible induction of inducible nitric oxide synthase (iNOS) gene with enhanced production of nitric oxide (NO) by intra-peritoneal injection of lipopolysaccharide (LPS) (a bacterial endotoxin), and (b) to determine the effects of hepatic cell volume changes due to anisotonicity or by infusion of certain metabolites, stress hormones and by induction of oxidative stress on production of NO from the iNOS-induced perfused liver of singhi catfish. Intra-peritoneal injection of LPS led to induction of iNOS gene and localized tissue specific expression of iNOS enzyme with more production and accumulation of NO in different tissues of singhi catfish. Further, changes of hydration status/cell volume, caused either by anisotonicity or by infusion of certain metabolites such as glutamine plus glycine and adenosine, affected the NO production from the perfused liver of iNOS-induced singhi catfish. In general, increase of hydration status/cell swelling due to hypotonicity caused decrease, and decrease of hydration status/cell shrinkage due to hypertonicity caused increase of NO efflux from the perfused liver, thus suggesting that changes in hydration status/cell volume of hepatic cells serve as a potent modulator for regulating the NO production. Significant increase of NO efflux from the perfused liver was also observed while infusing the liver with stress hormones like epinephrine and norepinephrine, accompanied with decrease of hydration status/cell volume of hepatic cells. Further, oxidative stress, caused due to infusion of t-butyl hydroperoxide and hydrogen peroxide separately, in the perfused liver of singhi catfish, resulted in

  3. Distributions and sea-to-air fluxes of nitrous oxide in the South China Sea and the West Philippines Sea

    NASA Astrophysics Data System (ADS)

    Tseng, Hsiao-Chun; Chen, Chen-Tung Arthur; Borges, Alberto V.; DelValls, T. Angel; Lai, Chao-Ming; Chen, Ting-Yu

    2016-09-01

    Approximately 600 water samples from the South China Sea (SCS) and 250 water samples from the West Philippines Sea (WPS) were collected during seven cruises from August 2003 to July 2007 to determine nitrous oxide (N2O) distributions between the surface and a maximum depth of 4250 m. In the SCS, the average surface N2O concentration exceeded the atmospheric equilibrium concentration (on average 132±23%); however in the WPS, the surface N2O concentration was lower than the atmospheric equilibrium concentration (on average 90±22%). The N2O concentration reached a maximum (~23 nmol L-1) in the WPS at 800-1000 m, and (~28 nmol L-1) at a shallower depth of around 600-800 m in the SCS, owing to vertical mixing and intensive upwelling in the SCS. In the SCS, the surface N2O concentration was 7.59±1.32 nmol L-1 and the calculated sea-to-air flux was 5.5±3.9 μmol m-2 d-1. The surface N2O concentration in the WPS, 5.19±1.26 nmol L-1, was lower than that in the SCS. The WPS is a sink for N2O and the calculated sea-to-air flux was -1.7±3.9 μmol m-2 d-1. The SCS emitted 19.3×106 mol d-1 N2O to the atmosphere and exported 8.5×106 mol d-1 N2O to the WPS during the wet season.

  4. Effect of inlet-air humidity, temperature, pressure, and reference Mach number on the formation of oxides of nitrogen in a gas turbine combustor

    NASA Technical Reports Server (NTRS)

    Marchionna, N. R.; Diehl, L. A.; Trout, A. M.

    1973-01-01

    Tests were conducted to determine the effect of inlet air humidity on the formation of oxides of nitrogen (NOx) from a gas turbine combustor. Combustor inlet air temperature ranged from 506 K (450 F) to 838 K (1050 F). The tests were primarily run at a constant pressure of 6 atmospheres and reference Mach number of 0.065. The NOx emission index was found to decrease with increasing inlet air humidity at a constant exponential rate: NOx = NOx0e-19H (where H is the humidity and the subscript 0 denotes the value at zero humidity). the emission index increased exponentially with increasing normalized inlet air temperature to the 1.14 power. Additional tests made to determine the effect of pressure and reference Mach number on NOx showed that the NOx emission index varies directly with pressure to the 0.5 power and inversely with reference Mach number.

  5. Elemental composition and oxidative properties of PM(2.5) in Estonia in relation to origin of air masses - results from the ECRHS II in Tartu.

    PubMed

    Orru, Hans; Kimmel, Veljo; Kikas, Ulle; Soon, Argo; Künzli, Nino; Schins, Roel P F; Borm, Paul J A; Forsberg, Bertil

    2010-03-01

    Fine particulate matter (PM(2.5)) was sampled at an urban background site in Tartu, Estonia over one-year period during the ECRHS II study. The elemental composition of 71 PM(2.5) samples was analyzed for different chemical elements using energy-dispersive X-ray fluorescence spectrometry (ED-XRF). The oxidative activity of 36 samples was assessed by measuring their ability to generate hydroxyl radicals in the presence of hydrogen peroxide. The origin of air masses was determined by computing 96-hour back trajectories of air masses with the HYSPLIT Model. The trajectories of air masses were divided into four sectors according to geographical patterns: "Russia," "Eastern Europe," "Western Europe," and "Scandinavia." During the study period, approximately 30% of air masses originated from "Scandinavia." The other three sectors had slightly lower values (between 18 and 22%). In spring, summer, and winter, higher total PM levels originated from air masses from continental areas, namely "Russia" and "Eastern Europe" (18.51+/-7.33 and 19.96+/-9.23microg m(-3), respectively). In autumn, the PM levels were highest in "Western Europe". High levels of Fe, Ti, and AlCaSi (Al, Ca, and Si) were also detected in air masses from the Eurasian continent. The oxidative properties were correlated to the origin of air masses. The OH values were approximately 1.5 times higher when air masses originated from the direction of "Eastern Europe" or "Russia." The origin of measured particles was evaluated using principal component factor analysis. When comparing the PM(2.5) elemental composition with seasonal variation, factor scores, and other studies, the factors represent: (1) combustion of biomass; (2) crustal dust; (3) traffic; and (4) power plants and industrial processes associated with oil burning. The total PM(2.5) is driven mainly by biomass and industrial combustion (63%) and other unidentified sources (23%). Other sources of PM, such as crustal dust and traffic, contribute a total

  6. Treatment of municipal landfill leachate by catalytic wet air oxidation: Assessment of the role of operating parameters by factorial design

    SciTech Connect

    Anglada, Angela; Urtiaga, Ane; Ortiz, Inmaculada; Diamadopoulos, Evan

    2011-08-15

    Highlights: > Landfill leachates can be treated effectively by catalytic wet oxidation. > Addition of H{sub 2}O{sub 2} in the presence of transition metals promotes degradation. > Factorial design evaluates the statistically significant operating conditions. > H{sub 2}O{sub 2}, reaction time and temperature are critical in determining performance. - Abstract: The wet air oxidation (WAO) of municipal landfill leachate catalyzed by cupric ions and promoted by hydrogen peroxide was investigated. The effect of operating conditions such as WAO treatment time (15-30 min), temperature (160-200 deg. C), Cu{sup 2+} concentration (250-750 mg L{sup -1}) and H{sub 2}O{sub 2} concentration (0-1500 mg L{sup -1}) on chemical oxygen demand (COD) removal was investigated by factorial design considering a two-stage, sequential process comprising the heating-up of the reactor and the actual WAO. The leachate, at an initial COD of 4920 mg L{sup -1}, was acidified to pH 3 leading to 31% COD decrease presumably due to the coagulation/precipitation of colloidal and other organic matter. During the 45 min long heating-up period of the WAO reactor under an inert atmosphere, COD removal values up to 35% (based on the initial COD value) were recorded as a result of the catalytic decomposition of H{sub 2}O{sub 2} to reactive hydroxyl radicals. WAO at 2.5 MPa oxygen partial pressure advanced treatment further; for example, 22 min of oxidation at 200 deg. C, 250 mg L{sup -1} Cu{sup 2+} and 0-1500 mg L{sup -1} H{sub 2}O{sub 2} resulted in an overall (i.e. including acidification and heating-up) COD reduction of 78%. Amongst the operating variables in question, temperature had the strongest influence on both the heating-up and WAO stages, while H{sub 2}O{sub 2} concentration strongly affected the former and reaction time the latter. Nonetheless, the effects of temperature and H{sub 2}O{sub 2} concentration were found to depend on the concentration levels of catalyst as suggested by the

  7. An experimental and numerical study of nitrogen oxide formation mechanisms in ammonia-hydrogen-air flames

    NASA Astrophysics Data System (ADS)

    Kumar, Praveen

    quantitatively. The NOx predictions by all the three chemical mechanisms are observed to be in fairly good agreement with the measured NOx, qualitatively, however predictions are found to be 3 to 4 times higher than the measurements for both lean and rich H 2/NH3 premixed flames. For laminar H2/NH3 diffusion flames, detailed 2-D comparisons of in-situ NO measurements with the 2-D simulated NO using the Tian, GRI-Mech3.0 and modified GRI-Mech chemical mechanisms are performed and found to differ from the measured NO by approximately an order of magnitude. For NH3 seeded H2/air diffusion flames, GRI-Mech3.0 seemed to overpredict NO by more than an order of magnitude and failed to capture the fundamental flame characteristics, such as the flame length variation with increasing NH3 in the fuel mixture. On the other hand, the predicted NO profiles by the Tian mechanism were not only found to be in better agreement with the measured NO, but they also captured the in-flame NO distribution as well, both qualitatively and quantitatively. Overall, the Tian mechanism is found to be the superior chemical mechanism to capture the NOx formation chemistry in NH3 seeded flames.

  8. In-situ, in air, high-temperature phase transformations in rare-earth niobates and titanium oxides (dysprosium and yttrium) using a thermal-image furnace

    NASA Astrophysics Data System (ADS)

    Siah, Lay Foong

    Thermal-image furnaces afford two major advantages over the conventional resistance heating systems for high-temperature studies of oxides in air, namely: (i) the highly localized heating allows temperatures in excess of 2500°C to be reached in air or in an oxidizing atmosphere, and (ii) no sample contamination from volatile furnace components since the sample is heated by absorption of a focused, high intensity light beam. In this work, we developed a compact furnace powered by four halogen infrared reflector lamps (150 W each), for in-situ high-temperature studies using synchrotron radiation. The primary objective was to evaluate the feasibility of the thermal-image technique for in-situ, in air, studies of high-temperature phase transformations in oxide ceramics. Specifically, the issues of temperature measurement and reliability of results obtained in comparison with published literature were addressed. The use of a co-existent "in-situ thermometer" was found to be a viable method to monitor the sample temperature in the image "hot-spot". Studies of YNbO4 and DyNbO4 revealed the existence of a new cubic phase at elevated temperatures beyond the commonly known ferroelastic monoclinic-to-paraelastic tetragonal transformations. A series of high-temperature powder patterns of the pure hexagonal phase of DY2TiO5 was also collected in-situ, in air.

  9. Characterization of air-formed surface oxide film on a Co-Ni-Cr-Mo alloy (MP35N) and its change in Hanks' solution

    NASA Astrophysics Data System (ADS)

    Nagai, Akiko; Tsutsumi, Yusuke; Suzuki, Yuta; Katayama, Keiichi; Hanawa, Takao; Yamashita, Kimihiro

    2012-05-01

    The air-formed surface oxide films used for stents were characterized to determine their composition and chemical state on a Co-Ni-Cr-Mo alloy. The change of the films in Hanks' solution was used to estimate the reconstruction of the film in the human body. Angle-resolved X-ray photoelectron spectroscopy was used to characterize the composition of the film and substrate, as well as the film's thickness. The surface oxide film on the Co-Ni-Cr-Mo alloy (when mechanically polished) consists of oxide species of cobalt, nickel, chromium, and molybdenum, contains a large amount of OH-, and has a thickness of approximately 2.5 nm. Cations exist in the oxide as Co2+, Ni2+, Cr3+, Mo4+, Mo5+, and Mo6+. Chromium is enriched and cobalt and nickel are depleted in the oxide; however, nickel is enriched and cobalt is depleted in the substrate alloy just under the surface oxide film. Concentration of chromium was low and that of nickel was high at small take-off angles. This indicates that distribution of chromium is greater in the inner layer, but nickel is distributed more in the outer layer of the surface oxide film. During immersion in Hanks' solution, cobalt and nickel dissolved, and the film composition changed to mostly chromium oxide (Cr3+), along with small amounts of cobalt, nickel, and molybdenum oxides, and calcium phosphate containing magnesium, potassium, and carbonate. After immersion in Hanks' solution, the thickness of the surface layer containing calcium phosphate increased to more than 4 nm, while the amount of OH- increased. The amount of cobalt and nickel in the surface oxide film and in the substrate alloy just below the oxide decreased during immersion.

  10. Ozonolysis of methyl oleate monolayers at the air-water interface: oxidation kinetics, reaction products and atmospheric implications.

    PubMed

    Pfrang, Christian; Sebastiani, Federica; Lucas, Claire O M; King, Martin D; Hoare, Ioan D; Chang, Debby; Campbell, Richard A

    2014-07-14

    Ozonolysis of methyl oleate monolayers at the air-water interface results in surprisingly rapid loss of material through cleavage of the C=C bond and evaporation/dissolution of reaction products. We determine using neutron reflectometry a rate coefficient of (5.7 ± 0.9) × 10(-10) cm(2) molecule(-1) s(-1) and an uptake coefficient of ∼3 × 10(-5) for the oxidation of a methyl ester monolayer: the atmospheric lifetime is ∼10 min. We obtained direct experimental evidence that <2% of organic material remains at the surface on atmospheric timescales. Therefore known long atmospheric residence times of unsaturated fatty acids suggest that these molecules cannot be present at the interface throughout their ageing cycle, i.e. the reported atmospheric longevity is likely to be attributed to presence in the bulk and viscosity-limited reactive loss. Possible reaction products were characterized by ellipsometry and uncertainties in the atmospheric fate of organic surfactants such as oleic acid and its methyl ester are discussed. Our results suggest that a minor change to the structure of the molecule (fatty acid vs. its methyl ester) considerably impacts on reactivity and fate of the organic film. PMID:24870051

  11. Flexible high power-per-weight perovskite solar cells with chromium oxide-metal contacts for improved stability in air.

    PubMed

    Kaltenbrunner, Martin; Adam, Getachew; Głowacki, Eric Daniel; Drack, Michael; Schwödiauer, Reinhard; Leonat, Lucia; Apaydin, Dogukan Hazar; Groiss, Heiko; Scharber, Markus Clark; White, Matthew Schuette; Sariciftci, Niyazi Serdar; Bauer, Siegfried

    2015-10-01

    Photovoltaic technology requires light-absorbing materials that are highly efficient, lightweight, low cost and stable during operation. Organolead halide perovskites constitute a highly promising class of materials, but suffer limited stability under ambient conditions without heavy and costly encapsulation. Here, we report ultrathin (3 μm), highly flexible perovskite solar cells with stabilized 12% efficiency and a power-per-weight as high as 23 W g(-1). To facilitate air-stable operation, we introduce a chromium oxide-chromium interlayer that effectively protects the metal top contacts from reactions with the perovskite. The use of a transparent polymer electrode treated with dimethylsulphoxide as the bottom layer allows the deposition-from solution at low temperature-of pinhole-free perovskite films at high yield on arbitrary substrates, including thin plastic foils. These ultra-lightweight solar cells are successfully used to power aviation models. Potential future applications include unmanned aerial vehicles-from airplanes to quadcopters and weather balloons-for environmental and industrial monitoring, rescue and emergency response, and tactical security applications. PMID:26301766

  12. Wet air oxidation of resorcinol as a model treatment for refractory organics in wastewaters from the wood processing industry.

    PubMed

    Weber, Bernd; Chavez, Alma; Morales-Mejia, Julio; Eichenauer, Sabrina; Stadlbauer, Ernst A; Almanza, Rafael

    2015-09-15

    Wastewater treatment systems are important tools to enhance sustainability in terms of reducing environmental impact and complying with sanitary requirements. This work addresses the wet air oxidation (WAO) process for pre-treatment of phenolic wastewater effluents. The aim was to increase biodegradability prior to a subsequent anaerobic stage. In WAO laboratory experiments using a micro-autoclave, the model compound resorcinol was degraded under different oxygen availability regims within the temperature range 150 °C-270 °C. The activation energy was determined to be 51.5 kJ/mol. Analysis of the products revealed that after 3 h of reaction at 230 °C, 97.5% degradation of resorcinol was achieved. At 250 °C and the same reaction time complete removal of resorcinol was observed. In this case the total organic carbon content was reduced down to 29%, from 118.0 mg/L down to 34.4 mg/L. Under these process conditions, the pollutant was only partially mineralized and the ratio of the biological oxygen demand relative to the chemical oxygen demand, which is 0.07 for resorcinol, was increased to a value exceeding 0.5. The main by-product acetic acid, which is a preferred compound for methanogenic bacteria, was found to account for 33% of the total organic carbon. PMID:26164636

  13. Flexible high power-per-weight perovskite solar cells with chromium oxide-metal contacts for improved stability in air

    NASA Astrophysics Data System (ADS)

    Kaltenbrunner, Martin; Adam, Getachew; Głowacki, Eric Daniel; Drack, Michael; Schwödiauer, Reinhard; Leonat, Lucia; Apaydin, Dogukan Hazar; Groiss, Heiko; Scharber, Markus Clark; White, Matthew Schuette; Sariciftci, Niyazi Serdar; Bauer, Siegfried

    2015-10-01

    Photovoltaic technology requires light-absorbing materials that are highly efficient, lightweight, low cost and stable during operation. Organolead halide perovskites constitute a highly promising class of materials, but suffer limited stability under ambient conditions without heavy and costly encapsulation. Here, we report ultrathin (3 μm), highly flexible perovskite solar cells with stabilized 12% efficiency and a power-per-weight as high as 23 W g-1. To facilitate air-stable operation, we introduce a chromium oxide-chromium interlayer that effectively protects the metal top contacts from reactions with the perovskite. The use of a transparent polymer electrode treated with dimethylsulphoxide as the bottom layer allows the deposition--from solution at low temperature--of pinhole-free perovskite films at high yield on arbitrary substrates, including thin plastic foils. These ultra-lightweight solar cells are successfully used to power aviation models. Potential future applications include unmanned aerial vehicles--from airplanes to quadcopters and weather balloons--for environmental and industrial monitoring, rescue and emergency response, and tactical security applications.

  14. Characterization of Binary Ag-Cu Ion Mixtures in Zeolites: Their Reduction Products and Stability to Air Oxidation

    SciTech Connect

    Fiddy, Steven; Petranovskii, Vitalii; Ogden, Steve; Iznaga, Inocente Rodriguez

    2007-02-02

    A series of Ag+-Cu2+ binary mixtures with different Ag/Cu ratios were supported on mordenite with different Si/Al ratios and were subsequently reduced under hydrogen in the temperature range 323K - 473K. Ag and Cu K-edge X-ray Absorption Spectroscopy (XAS) was conducted on these systems in-situ to monitor the reduction species formed and the kinetics of their reduction. In-situ XANES clearly demonstrates that the formation of silver particles is severely impeded by the addition of copper and that the copper is converted from Cu(II) to Cu(I) during reduction and completely reverts back to Cu(II) during cooling. There are no indications at any stage of the formation of bimetallic Ag-Cu clusters. Interestingly, the Ag/Cu ratio appears to have no influence of the reduction kinetics and reduction products formed with only the highest Si/Al ratio (MR = 128) investigated during this study having an influence on the reduction and stability to air oxidation.

  15. Influences of Different Components on Agglomeration Behavior of MoS2 During Oxidation Roasting Process in Air

    NASA Astrophysics Data System (ADS)

    Wang, Lu; Zhang, Guo-Hua; Wang, Jing-Song; Chou, Kuo-Chih

    2016-08-01

    An agglomeration of the furnace charge always takes place during the oxidation roasting process of molybdenite concentrate (with the main component of MoS2) in multiple hearth furnaces, which greatly affects the production process and furnace service life. In the present work, a preliminary study about the influence of various components on the agglomeration phenomenon of pure MoS2 have been carried out. The results show that reaction temperature, impurity content, and air flow rate have significant effects on the agglomeration extent. Meanwhile, the impurity type added into the pure MoS2 plays a crucial role. It was found that CaO and MgO have a stronger sulfur-fixing effect and that the desulphurization of the roasted product was uncompleted. It was also concluded that the agglomeration is due to the formation of low-melting-point eutectics, including that between MoO3 and impurities and that between MoO3 and Mo4O11. It is suggested that decreasing the impurities contents, especially K, Cu, Pb, and Fe, is an effective method for reducing the extent of agglomeration.

  16. Tailoring indium oxide nanocrystal synthesis conditions for air-stable high-performance solution-processed thin-film transistors.

    PubMed

    Swisher, Sarah L; Volkman, Steven K; Subramanian, Vivek

    2015-05-20

    Semiconducting metal oxides (ZnO, SnO2, In2O3, and combinations thereof) are a uniquely interesting family of materials because of their high carrier mobilities in the amorphous and generally disordered states, and solution-processed routes to these materials are of particular interest to the printed electronics community. Colloidal nanocrystal routes to these materials are particularly interesting, because nanocrystals may be formulated with tunable surface properties into stable inks, and printed to form devices in an additive manner. We report our investigation of an In2O3 nanocrystal synthesis for high-performance solution-deposited semiconductor layers for thin-film transistors (TFTs). We studied the effects of various synthesis parameters on the nanocrystals themselves, and how those changes ultimately impacted the performance of TFTs. Using a sintered film of solution-deposited In2O3 nanocrystals as the TFT channel material, we fabricated devices that exhibit field effect mobility of 10 cm(2)/(V s) and an on/off current ratio greater than 1 × 10(6). These results outperform previous air-stable nanocrystal TFTs, and demonstrate the suitability of colloidal nanocrystal inks for high-performance printed electronics. PMID:25915094

  17. Influences of Different Components on Agglomeration Behavior of MoS2 During Oxidation Roasting Process in Air

    NASA Astrophysics Data System (ADS)

    Wang, Lu; Zhang, Guo-Hua; Wang, Jing-Song; Chou, Kuo-Chih

    2016-05-01

    An agglomeration of the furnace charge always takes place during the oxidation roasting process of molybdenite concentrate (with the main component of MoS2) in multiple hearth furnaces, which greatly affects the production process and furnace service life. In the present work, a preliminary study about the influence of various components on the agglomeration phenomenon of pure MoS2 have been carried out. The results show that reaction temperature, impurity content, and air flow rate have significant effects on the agglomeration extent. Meanwhile, the impurity type added into the pure MoS2 plays a crucial role. It was found that CaO and MgO have a stronger sulfur-fixing effect and that the desulphurization of the roasted product was uncompleted. It was also concluded that the agglomeration is due to the formation of low-melting-point eutectics, including that between MoO3 and impurities and that between MoO3 and Mo4O11. It is suggested that decreasing the impurities contents, especially K, Cu, Pb, and Fe, is an effective method for reducing the extent of agglomeration.

  18. Numerical studies of nitric oxide formation in nanosecond-pulsed discharge-stabilized flames of premixed methane/air.

    PubMed

    Bak, Moon Soo; Cappelli, Mark A

    2015-08-13

    A simulation is developed to investigate the kinetics of nitric oxide (NO) formation in premixed methane/air combustion stabilized by nanosecond-pulsed discharges. The simulation consists of two connected parts. The first part calculates the kinetics within the discharge while considering both plasma/combustion reactions and species diffusion, advection and thermal conduction to the surrounding flow. The second part calculates the kinetics of the overall flow after mixing the discharge flow with the surrounding flow to account for the effect that the discharge has on the overall kinetics. The simulation reveals that the discharge produces a significant amount of atomic oxygen (O) as a result of the high discharge temperature and dissociative quenching of excited state nitrogen by molecular oxygen. This atomic oxygen subsequently produces hydroxyl (OH) radicals. The fractions of these O and OH then undergo Zel'dovich reactions and are found to contribute to as much as 73% of the total NO that is produced. The post-discharge simulation shows that the NO survives within the flow once produced. PMID:26170428

  19. Air Pollution Upregulates Endothelial Cell Procoagulant Activity Via Ultrafine Particle-Induced Oxidant Signaling and Tissue Factor Expression

    EPA Science Inventory

    Air pollution exposure is associated with cardiovascular events triggered by clot formation. Endothelial activation and initiation of coagulation are pathophysiological mechanisms that could link inhaled air pollutants to vascular events. Here we investigated the underlying mecha...

  20. Distribution and Sea-to-air Flux of Nitrous Oxide in the East China Sea during the Summer of 2013

    NASA Astrophysics Data System (ADS)

    Wang, Lan; Zhang, Guiling; Zhu, Zhuoyi; Li, Jia; Liu, Sumei; Ye, Wangwang; Han, Yu

    2016-07-01

    Dissolved nitrous oxide (N2O) at different depths of 73 stations in the Changjiang (Yangtze River) Estuary and the East China Sea (ECS) were determined from August 4 to 31 of 2013, and the sea-to-air fluxes of N2O were also estimated in this study. N2O concentrations in the surface waters ranged from 6.33 to 44.40 nmol L-1 with an average of (9.27±4.30) nmol L-1 and the values in the bottom waters ranged from 5.19 to 26.98 nmol L-1 with an average of (11.87±3.71) nmol L-1. The concentrations of N2O decreased with distance from the Changjiang Estuary to the open sea. The vertical distributions of N2O indicated great spatial variations. A region of significant bottom-water hypoxia, with oxygen concentration less than 1.5 mg L-1, occurred at the north of the ECS, and increased bottom N2O concentrations was observed. Frequent vertical mixing may enhance the emission of N2O from this hypoxic area. N2O in the surface waters of all stations were over-saturated, and the N2O saturations ranged from 106% to 658%, with an average of (149±62)%. We estimated the sea-to-air fluxes of N2O as (30.6±59.1) μmol m-2 d-1 from the Changjiang Estuary, (9.8±8.8) μmol m-2 d-1 from the coastal and shelf, and (21.0±12.7) μmol m-2 d-1 from the continental slope using the Wanninkhof 1992 equation, (24.9±47.2) μmol m-2 d-1, (8.0±6.7) μmol m-2 d-1 and (16.5±9.6) μmol m-2 d-1 using the Nightingale 2000 equation, respectively. N2O emission from the ECS was estimated to be about (8.2-16.0)×10-2 Tg-N2O yr-1, suggesting that the ECS was a significant net source of atmospheric N2O.

  1. Alpha B-crystallin prevents the arrhythmogenic effects of particulate matter isolated from ambient air by attenuating oxidative stress

    SciTech Connect

    Park, Hyelim; Park, Sanghoon; Jeon, Hyunju; Song, Byeong-Wook; Kim, Jin-Bae; Kim, Chang-Soo; Pak, Hui-Nam; Hwang, Ki-Chul; Lee, Moon-Hyoung; Chung, Ji Hyung; Joung, Boyoung

    2013-01-15

    Ca{sup 2+}/calmodulin-dependent protein kinase II (CaMKII) is activated by particulate matter (PM) isolated from ambient air and linked to prolonged repolarization and cardiac arrhythmia. We evaluated whether alpha B-crystallin (CryAB), a heat shock protein, could prevent the arrhythmogenic effects of PM by preventing CaMKII activation. CryAB was delivered into cardiac cells using a TAT-protein transduction domain (TAT-CryAB). ECGs were measured before and after tracheal exposure of diesel exhaust particles (DEP) and each intervention in adult Sprague–Dawley rats. After endotracheal exposure of DEP (200 μg/mL for 30 minutes, n = 11), QT intervals were prolonged from 115 ± 14 ms to 144 ± 20 ms (p = 0.03), and premature ventricular contractions were observed more frequently (0% vs. 44%) than control (n = 5) and TAT-Cry (n = 5). However, DEP-induced arrhythmia was not observed in TAT-CryAB (1 mg/kg) pretreated rats (n = 5). In optical mapping of Langendorff-perfused rat heats, compared with baseline, DEP infusion of 12.5 μg/mL (n = 12) increased apicobasal action potential duration (APD) differences from 2 ± 6 ms to 36 ± 15 ms (p < 0.001), APD restitution slope from 0.26 ± 0.07 to 1.19 ± 0.11 (p < 0.001) and ventricular tachycardia (VT) from 0% to 75% (p < 0.001). DEP infusion easily induced spatially discordant alternans. However, the effects of DEP were prevented by TAT-CryAB (1 mg/kg, n = 9). In rat myocytes, while DEP increased reactive oxygen species (ROS) generation and phosphated CaMKII, TAT-CryAB prevented these effects. In conclusion, CryAB, a small heat shock protein, might prevent the arrhythmogenic effects of PM by attenuating ROS generation and CaMKII activation. -- Highlights: ► Particulate matter (PM) increases arrhythmia. ► PM induced arrhythmias are related with oxidative stress and CaMKII activation. ► Alpha B-crystallin (CryAB) could attenuate the arrhythmogenic effect of PM. ► CryAB decreases oxidative stress and CaMKII activation

  2. Combined hydrolysis acidification and bio-contact oxidation system with air-lift tubes and activated carbon bioreactor for oilfield wastewater treatment.

    PubMed

    Guo, Chunmei; Chen, Yi; Chen, Jinfu; Wang, Xiaojun; Zhang, Guangqing; Wang, Jingxiu; Cui, Wenfeng; Zhang, Zhongzhi

    2014-10-01

    This paper investigated the enhancement of the COD reduction of an oilfield wastewater treatment process by installing air-lift tubes and adding an activated carbon bioreactor (ACB) to form a combined hydrolysis acidification and bio-contact oxidation system with air-lift tubes (HA/air-lift BCO) and an ACB. Three heat-resistant bacterial strains were cultivated and subsequently applied in above pilot plant test. Installing air-lift tubes in aerobic tanks reduced the necessary air to water ratio from 20 to 5. Continuous operation of the HA/air-lift BCO system for 2 months with a hydraulic retention time of 36 h, a volumetric load of 0.14 kg COD/(m(3)d) (hydrolysis-acidification or anaerobic tank), and 0.06 kg COD/(m(3)d) (aerobic tanks) achieved an average reduction of COD by 60%, oil and grease by 62%, total suspended solids by 75%, and sulfides by 77%. With a COD load of 0.56 kg/(m(3)d), the average COD in the ACB effluent was 58 mg/L. PMID:25105268

  3. Toxicity of copper oxide nanoparticles in lung epithelial cells exposed at the air-liquid interface compared with in vivo assessment

    PubMed Central

    Jing, Xuefang; Park, Jae Hong; Peters, Thomas M.; Thorne, Peter S.

    2015-01-01

    The toxicity of spark-generated copper oxide nanoparticles (CuONPs) was evaluated in human bronchial epithelial cells (HBEC) and lung adenocarcinoma cells (A549 cells) using an in vitro air-liquid interface (ALI) exposure system. Dose-response results were compared to in vivo inhalation and instillation studies of CuONP. Cells were exposed to particle-free clean air (controls) or spark-generated CuONPs. The number median diameter, geometric standard deviation and total number concentration of CuONPs were 9.2 nm, 1.48 and 2.27×107 particles/cm3, respectively. Outcome measures included cell viability, cytotoxicity, oxidative stress and proinflammatory chemokine production. Exposure to clean air (2 or 4 hr) did not induce toxicity in HBEC or A549 cells. Compared with controls, CuONP exposures significantly reduced cell viability, increased lactate dehydrogenase (LDH) release and elevated levels of reactive oxygen species (ROS) and IL-8 in a dose-dependent manner. A549 cells were significantly more susceptible to CuONP effects than HBEC. Antioxidant treatment reduced CuONP-induced cytotoxicity. When dose was expressed per area of exposed epithelium there was good agreement of toxicity measures with murine in vivo studies. This demonstrates that in vitro ALI studies can provide meaningful data on nanotoxicity of metal oxides. PMID:25575782

  4. Evaluation of retrofit crankcase ventilation controls and diesel oxidation catalysts for reducing air pollution in school buses

    NASA Astrophysics Data System (ADS)

    Trenbath, Kim; Hannigan, Michael P.; Milford, Jana B.

    2009-12-01

    This study evaluates the effect of retrofit closed crankcase ventilation filters (CCFs) and diesel oxidation catalysts (DOCs) on the in-cabin air quality in transit-style diesel school buses. In-cabin pollution levels were measured on three buses from the Pueblo, CO District 70 fleet. Monitoring was conducted while buses were driven along their regular routes, with each bus tested three times before and three times after installation of control devices. Ultrafine number concentrations in the school bus cabins were 33-41% lower, on average, after the control devices were installed. Mean mass concentrations of particulate matter less than 2.5 μm in diameter (PM2.5) were 56% lower, organic carbon (OC) 41% lower, elemental carbon (EC) 85% lower, and formaldehyde 32% lower after control devices were installed. While carbon monoxide concentrations were low in all tests, mean concentrations were higher after control devices were installed than in pre-retrofit tests. Reductions in number, OC, and formaldehyde concentrations were statistically significant, but reductions in PM2.5 mass were not. Even with control devices installed, during some runs PM2.5 and OC concentrations in the bus cabins were elevated compared to ambient concentrations observed in the area. OC concentrations inside the bus cabins ranged from 22 to 58 μg m -3 before and 13 to 33 μg m -3 after control devices were installed. OC concentrations were correlated with particle-bound organic tracers for lubricating oil emissions (hopanes) and diesel fuel and tailpipe emissions (polycyclic aromatic hydrocarbons (PAH) and aliphatic hydrocarbons). Mean concentrations of hopanes, PAH, and aliphatic hydrocarbons were lower by 37, 50, and 43%, respectively, after the control devices were installed, suggesting that both CCFs and DOCs were effective at reducing in-cabin OC concentrations.

  5. Long-Term Oxidation of Candidate Cast Iron and Advanced Austenitic Stainless Steel Exhaust System Alloys from 650-800 C in Air with Water Vapor

    DOE PAGESBeta

    Brady, Michael P; Muralidharan, Govindarajan; Leonard, Donovan N; Haynes, James A

    2014-01-01

    The oxidation behavior of SiMo cast iron, Ni-resist D5S cast iron, cast chromia-forming austenitic stainless steels of varying Cr/Ni content based on CF8C plus, HK, and HP, and a developmental cast alumina-forming austenitic (AFA) stainless steel of interest for diesel exhaust system components were studied for up to 5000 h at 650-800 C in air with 10% H2O. At 650 C, the Ni-resist D5S exhibited moderately better oxidation resistance than did the SiMo cast iron. However, the D5S suffered from oxide scale spallation issues at 700 C and higher, whereas the oxide scales formed on SiMo cast iron remained adherentmore » from 700-800 C despite oxide scales hundreds of microns thick. The oxidation of the SiMo cast iron exhibited unusual temperature dependence, with periods of slower oxidation kinetics at 750-800 C compared to 650-700 C due to continuous silica-rich scale formation at the higher temperatures. The oxidation of the cast chromia-forming austenitics trended with the level of Cr and Ni additions, with small mass losses consistent with Cr oxy-hydroxide volatilization processes for the higher 25Cr/25-35Ni HK and HP type alloys, and transition to rapid Fe-base oxide formation and scale spallation in the lower 19Cr/12Ni CF8C plus type alloy. In contrast, small positive mass changes consistent with protective alumina scale formation were observed for the cast AFA alloy under all conditions studied. Implications of these findings for diesel exhaust system components are discussed.« less

  6. Long-term oxidation of candidate cast iron and stainless steel exhaust system alloys from 650 to 800 °C in air with water vapor

    SciTech Connect

    Brady, Michael P.; Muralidharan, Govindarajan; Leonard, Donovan .; Haynes, James A.; Weldon, R. G.; England, R. D.

    2014-08-29

    Here, the oxidation behavior of SiMo cast iron, Ni-resist D5S cast iron, cast chromia-forming austenitic stainless steels of varying Cr/Ni content based on CF8C plus, HK, and HP, and a developmental cast alumina-forming austenitic (AFA) stainless steel of interest for diesel exhaust system components were studied for up to 5000 h at 650-800 °C in air with 10% H2O. At 650 °C, the Ni-resist D5S exhibited moderately better oxidation resistance than did the SiMo cast iron. However, the D5S suffered from oxide scale spallation issues at 700 °C and higher, whereas the oxide scales formed on SiMo cast iron remained adherent from 700-800 °C despite oxide scales hundreds of microns thick. The oxidation of the SiMo cast iron exhibited unusual temperature dependence, with periods of slower oxidation kinetics at 750-800 °C compared to 650-700 °C due to continuous silica-rich scale formation at the higher temperatures. The oxidation of the cast chromia-forming austenitics trended with the level of Cr and Ni additions, with small mass losses consistent with Cr oxy-hydroxide volatilization processes for the higher 25Cr/25-35Ni HK and HP type alloys, and transition to rapid Fe-base oxide formation and scale spallation in the lower 19Cr/12Ni CF8C plus type alloy. In contrast, small positive mass changes consistent with protective alumina scale formation were observed for the cast AFA alloy under all conditions studied. Implications of these findings for diesel exhaust system components are discussed.

  7. Long-term oxidation of candidate cast iron and stainless steel exhaust system alloys from 650 to 800 °C in air with water vapor

    DOE PAGESBeta

    Brady, Michael P.; Muralidharan, Govindarajan; Leonard, Donovan .; Haynes, James A.; Weldon, R. G.; England, R. D.

    2014-08-29

    Here, the oxidation behavior of SiMo cast iron, Ni-resist D5S cast iron, cast chromia-forming austenitic stainless steels of varying Cr/Ni content based on CF8C plus, HK, and HP, and a developmental cast alumina-forming austenitic (AFA) stainless steel of interest for diesel exhaust system components were studied for up to 5000 h at 650-800 °C in air with 10% H2O. At 650 °C, the Ni-resist D5S exhibited moderately better oxidation resistance than did the SiMo cast iron. However, the D5S suffered from oxide scale spallation issues at 700 °C and higher, whereas the oxide scales formed on SiMo cast iron remainedmore » adherent from 700-800 °C despite oxide scales hundreds of microns thick. The oxidation of the SiMo cast iron exhibited unusual temperature dependence, with periods of slower oxidation kinetics at 750-800 °C compared to 650-700 °C due to continuous silica-rich scale formation at the higher temperatures. The oxidation of the cast chromia-forming austenitics trended with the level of Cr and Ni additions, with small mass losses consistent with Cr oxy-hydroxide volatilization processes for the higher 25Cr/25-35Ni HK and HP type alloys, and transition to rapid Fe-base oxide formation and scale spallation in the lower 19Cr/12Ni CF8C plus type alloy. In contrast, small positive mass changes consistent with protective alumina scale formation were observed for the cast AFA alloy under all conditions studied. Implications of these findings for diesel exhaust system components are discussed.« less

  8. Graphene oxide electrocatalyst on MnO2 air cathode as an efficient electron pump for enhanced oxygen reduction in alkaline solution

    PubMed Central

    Basirun, Wan Jeffrey; Sookhakian, Mehran; Baradaran, Saeid; Endut, Zulkarnain; Mahmoudian, Mohammad Reza; Ebadi, Mehdi; Yousefi, Ramin; Ghadimi, Hanieh; Ahmed, Sohail

    2015-01-01

    Graphene oxide (GO) was deposited on the surface of a MnO2 air cathode by thermal evaporation at 50°C from a GO colloidal suspension. Fourier transformed infrared spectroscopy and field emission scanning electron microscopy confirmed the presence of GO on the MnO2 air cathode (GO-MnO2). Voltammetry and chrono-amperometry showed increased currents for the oxygen reduction reaction (ORR) in 6 M KOH solution for GO-MnO2 compared to the MnO2 cathode. The GO-MnO2 was used as an air cathode in an alkaline tin-air cell and produced a maximum power density of 13 mW cm−2, in contrast to MnO2, which produced a maximum power density of 9.2 mW cm−2. The electrochemical impedance spectroscopy results suggest that the chemical step for the ORR is the rate determining step, as proposed earlier by different researchers. It is suggested that the presence of GO and electrochemically reduced graphene oxide (ERGO) on the MnO2 surface are responsible for the increased rate of this step, whereby GO and ERGO accelerate the process of electron donation to the MnO2 and to adsorbed oxygen atoms. PMID:25765731

  9. Anomalous Oxide Charge Variation Identified by Alternating Current Surface Photovoltage Method in Cr-Aqueous-Solution-Rinsed p-Type Si(001) Wafers Exposed to Air

    NASA Astrophysics Data System (ADS)

    Shimizu, Hirofumi; Sanada, Yuji

    2011-11-01

    Chromium (Cr)-aqueous-solution-rinsed and/or hydrofluoric acid (HF)-solution-dipped p-type silicon (Si) (001) wafer surfaces are investigated by the frequency-dependent alternating current (AC) surface photovoltage (SPV) method. At the Cr(OH)3/p-type Si interface, in principle, a Schottky barrier could not possibly be generated. The Cr ion (Cr3+) is considered to forcibly deprive a p-type Si substrate of electrons during metallization (Cr3++3e-→Cr). Thus, at an early stage of air exposure, a positive fixed oxide charge may be compensated for by electrons, indicating the disappearance of AC SPV. With air exposure time, AC SPV emerges again and increases gradually in a Cr-deposited p-type Si(001) surface. This is because the native oxide between the Cr atom layer and the p-type Si substrate grows with time. As a result, a positive fixed oxide charge exceeds the overall charge state of the Cr-deposited p-type Si surface. Thus, AC SPV appears again and gradually increases with the fixed oxide charge in p-type Si. The saturated value is in a good agreement with that of the HF aqueous-solution-dipped p-type Si surface.

  10. Effects of oxidation on the impact energy of Hastelloy S and Hastelloy C-4 Charpy V-notch specimens heated in air at 600 to 800

    SciTech Connect

    Fullam, H.T.

    1981-01-01

    The /sup 90/SrF/sub 2/ heat source being developed at PNL utilizes a Hastelloy S or Hastelloy C-4 outer capsule having a 0.5-in.-thick wall to contain the Hastelloy C-276 inner capsule. The primary objective of the study was to demonstrate that the air oxidation of the outer capsule that could occur during heat-source service would not degrade the ductility and Charpy impact strength of the capsule below the licensing requirements given in Section 1.1. The /sup 90/SrF/sub 2/ heat source under development is intended for general-purpose use. Compatibility considerations limit the interface temperature between the /sup 90/SrF/sub 2/ and Hastelloy C-276 inner capsule to a maximum of 800/sup 0/C. The outer capsule surface temperature will be somewhat less than 800/sup 0/C, and depending on the service, may be substantially lower. The oxidation tests were therefore carried out at 600/sup 0/ to 800/sup 0/C for exposures up to 10,000h to cover the range of temperature the outer capsule might expect to encounter in service. The results showed that the oxidation of Hastelloy S and Hastelloy C-4 in air at 600/sup 0/ to 800/sup 0/C is very slow, and both alloys form adherent oxide layers that serve to protect the underlying metal. Subsurface attack of Hastelloy S and Hastelloy C-4 due to oxidation was greater than expected, considering the slow oxidation rates of the two alloys at 600/sup 0/ to 800/sup 0/C. Estimates of subsurface attack, determined from micrographs of the oxidized specimens, showed erratic results and it was impossible to assign any type of rate equation to the subsurface attack. A conservative estimate of long-term effects can be made using a linear extrapolation of the test results. There were no significant differences between the room-temperature Charpy impact energy of Hastelloy S and Hastelloy C-4 specimens oxidized in air at 600/sup 0/ to 800/sup 0/C and control specimens heated in vacuum.

  11. A convenient N2-CCl4 mixture plasma treatment to improve TiO2 photocatalytic oxidation of aromatic air contaminants under both UV and visible light

    NASA Astrophysics Data System (ADS)

    Hu, Shaozheng; Li, Fayun; Fan, Zhiping

    2013-12-01

    A convenient N2-CCl4 mixture plasma treatment to improve TiO2 photocatalytic oxidation of aromatic air contaminants under both UV and visible light was reported. X-ray diffraction (XRD), N2 adsorption, UV-vis spectroscopy, photoluminescence (PL), and X-ray photoelectron spectroscopy (XPS) were used to characterize the prepared TiO2 catalysts. The microstructures of the TiO2 catalysts were preserved after plasma treatments. Chlorine ions did not doped into TiO2 lattice but located on TiO2 surface via the coordination with Ti4+ sites. The doping N content of prepared TiO2 catalyst increased obviously by using this N2-CCl4 mixture plasma method. The activities were tested in the photocatalytic oxidation of benzene and toluene under both UV and visible light. Chlorine radicals which formed under illumination are effective in oxidizing aromatic side groups, but ineffective in reactions with the aromatic ring.

  12. Gaseous and Particulate Oxidation Products Analysis of a Mixture of a-pinene + b-pinene/O3/Air in the Absence of Light and a-pinene + b-pinene/NOx/Air in the Presence of Natural Sunlight

    NASA Astrophysics Data System (ADS)

    Jaoui, M.; Kamens, R.

    2001-12-01

    The gas and particle phase reaction products of a mixture of the atmospherically important terpenes a-pinene and b-pinene with the atmospheric oxidants O3 and OHNOx were investigated using both gas chromatography-mass spectrometry (GC-MS) and high performance liquid chromatography (HPLC) for identification and quantification of reaction products. The nighttime oxidation of a mixture of a-pinene and b-pinene in the presence of O3air, and the daytime oxidation of a mixture of a-pinene + b-pinene with NOx/air in the presence of natural sunlight were carried out in the University of North Carolina's large outdoor smog chamber (190 m3) located in Chatham County, North Carolina. Mass balances for gaseous and aerosol reaction products are reported over the course of the reaction. More than twenty-nine products were identified and/or quantified in this study. On average, measured gas and particle phase products accounted for ~74 to ~80% of the reacted a-pineneb-pinene mixture carbon. Measurements show that a number of reaction products were found in both O3 and NOx system [pinonaldehyde, pinic acid, pinonic acid, pinalic-3-acid, 4-hydroxypinalic-3-acid, 4-oxonopinone, 1-hydroxy-nopinone, 3-hydroxy-nopinone, and nopinone]. Pinonic acid, pinic acid, pinalic-3-acid, 4-hydroxypinalic-3-acid, and 10-hydroxypinonic acid were observed in the early stage in the aerosol phase and may play an important role in the early formation of secondary aerosols.

  13. High-Temperature Oxidation Resistance of a Nanoceria Spray-Coated 316L Stainless Steel Under Short-Term Air Exposure

    NASA Astrophysics Data System (ADS)

    Lopez, Hugo F.; Mendoza, Humberto; Church, Ben

    2013-10-01

    Nanoceria coatings using a spray method were implemented on a 316L stainless steel (SS). Coated and uncoated coupons were exposed to dry air at 1073 K to 1273 K (800 °C to 1000 °C) for short time periods (up to 24 hours) and in situ measurements of oxidation were carried out using a highly sensitive thermogravimetric balance. From the experimental outcome, activation energies were determined in both, coated and uncoated 316 SS coupons. The estimated exhibited activation energies for oxidation in the coated and uncoated conditions were 174 and 356 kJ/mol, respectively. In addition, the developed scales were significantly different. In the coated steel, the dominant oxide was an oxide spinel (Fe, Mn)3O4 and the presence of Fe2O3 was sharply reduced, particularly at 1273 K (1000 °C). In contrast, no spinel was found in the uncoated 316L SS, and Fe2O3 was always present in the scale at all the investigated oxidation temperatures. The coated steels developed a highly adherent fine-grained scale structure. Apparently, the nanoceria particles enhanced nucleation of the newly formed scale while restricting coarsening. Coarse grain structures were found in the uncoated steels with scale growth occurring at grain ledges. Moreover, the oxidation rates for the coated 316L SS were at least an order of magnitude lower than those exhibited by the steel in the uncoated condition. The reduction in oxidation rates is attributed to a shift in the oxidation mechanism from outward cation diffusion to inward oxygen diffusion.

  14. Assessing the air quality impact of nitrogen oxides and benzene from road traffic and domestic heating and the associated cancer risk in an urban area of Verona (Italy)

    NASA Astrophysics Data System (ADS)

    Schiavon, Marco; Redivo, Martina; Antonacci, Gianluca; Rada, Elena Cristina; Ragazzi, Marco; Zardi, Dino; Giovannini, Lorenzo

    2015-11-01

    Simulations of emission and dispersion of nitrogen oxides (NOx) are performed in an urban area of Verona (Italy), characterized by street canyons and typical sources of urban pollutants. Two dominant source categories are considered: road traffic and, as an element of novelty, domestic heaters. Also, to assess the impact of urban air pollution on human health and, in particular, the cancer risk, simulations of emission and dispersion of benzene are carried out. Emissions from road traffic are estimated by the COPERT 4 algorithm, whilst NOx emission factors from domestic heaters are retrieved by means of criteria provided in the technical literature. Then maps of the annual mean concentrations of NOx and benzene are calculated using the AUSTAL2000 dispersion model, considering both scenarios representing the current situation, and scenarios simulating the introduction of environmental strategies for air pollution mitigation. The simulations highlight potentially critical situations of human exposure that may not be detected by the conventional network of air quality monitoring stations. The proposed methodology provides a support for air quality policies, such as planning targeted measurement campaigns, re-locating monitoring stations and adopting measures in favour of better air quality in urban planning. In particular, the estimation of the induced cancer risk is an important starting point to conduct zoning analyses and to detect the areas where population is more directly exposed to potential risks for health.

  15. CONDENSED MATTER: ELECTRONIC STRUCTURE, ELECTRICAL, MAGNETIC, AND OPTICAL PROPERTIES: A Novel Fully Depleted Air AlN Silicon-on-Insulator Metal-Oxide-Semiconductor Field Effect Transistor

    NASA Astrophysics Data System (ADS)

    Yang, Yuan; Gao, Yong; Gong, Peng-Liang

    2008-08-01

    A novel fully depleted air AlN silicon-on-insulator (SOI) metal-oxide-semiconductor field effect transistor (MOS-FET) is presented, which can eliminate the self-heating effect and solve the problem that the off-state current of SOI MOSFETs increases and the threshold voltage characteristics become worse when employing a high thermal conductivity material as a buried layer. The simulation results reveal that the lattice temperature in normal SOI devices is 75 K higher than the atmosphere temperature, while the lattice temperature is just 4K higher than the atmosphere temperature resulting in less severe self-heating effect in air AlN SOI MOSFETs and AlN SOI MOSFETs. The on-state current of air AlN SOI MOSFETs is similar to the AlN SOI structure, and improves 12.3% more than that of normal SOI MOSFETs. The off-state current of AlN SOI is 6.7 times of normal SOI MOSFETs, while the counterpart of air AlN SOI MOSFETs is lower than that of SOI MOSFETs by two orders of magnitude. The threshold voltage change of air AlN SOI MOSFETs with different drain voltage is much less than that of AlN SOI devices, when the drain voltage is biased at 0.8 V, this difference is 28mV, so the threshold voltage change induced by employing high thermal conductivity material is cured.

  16. Improvement of performance in low temperature solid oxide fuel cells operated on ethanol and air mixtures using Cu-ZnO-Al2O3 catalyst layer

    NASA Astrophysics Data System (ADS)

    Morales, M.; Espiell, F.; Segarra, M.

    2015-10-01

    Anode-supported single-chamber solid oxide fuel cells with and without Cu-ZnO-Al2O3 catalyst layers deposited on the anode support have been operated on ethanol and air mixtures. The cells consist of gadolinia-doped ceria electrolyte, Ni-doped ceria anode, and La0.6Sr0.4CoO3-δ-doped ceria cathode. Catalyst layers with different Cu-ZnO-Al2O3 ratios are deposited and sintered at several temperatures. Since the performance of single-chamber fuel cells strongly depends on catalytic properties of electrodes for partial oxidation of ethanol, the cells are electrochemically characterized as a function of the temperature, ethanol-air molar ratio and gas flow rate. In addition, catalytic activities of supported anode, catalytic layer-supported anode and cathode for partial oxidation of ethanol are analysed. Afterwards, the effect of composition and sintering temperature of catalyst layer on the cell performance are determined. The results indicate that the cell performance can be significantly enhanced using catalyst layers of 30:35:35 and 40:30:30 wt.% Cu-ZnO-Al2O3 sintered at 1100 °C, achieving power densities above 50 mW cm-2 under 0.45 ethanol-air ratio at temperatures as low as 450 °C. After testing for 15 h, all cells present a gradual loss of power density, without carbon deposition, which is mainly attributed to the partial re-oxidation of Ni at the anode.

  17. TASK TECHNICAL AND QUALITY ASSURANCE PLAN FOR OUT-OF-TANK DESTRUCTION OF TETRAPHENYLBORATE VIA WET AIR OXIDATION TECHNOLOGY: PHASE I - BENCH SCALE TESTS

    SciTech Connect

    Adu-Wusu, K

    2006-03-31

    Tank 48H return to service is critical to the processing of high level waste (HLW) at Savannah River Site (SRS). Liquid Waste Disposition (LWD) management has the goal of returning Tank 48H to routine service by January 2010 or as soon as practical. Tank 48H currently holds legacy material containing organic tetraphenylborate (TPB) compounds from the operation of the In-Tank Precipitation process. This material is not compatible with the waste treatment facilities at SRS and must be removed or undergo treatment to destroy the organic compounds before the tank can be returned to Tank Farm service. Tank 48H currently contains {approx}240,000 gallons of alkaline slurry with about 2 wt % potassium and cesium tetraphenylborate (KTPB and CsTPB). The main radioactive component in Tank 48H is {sup 137}Cs. The waste also contains {approx}0.15 wt % Monosodium Titanate (MST) which has adsorbed {sup 90}Sr, U, and Pu isotopes. A System Engineering Evaluation of technologies/ideas for the treatment of TPB identified Wet Air Oxidation (WAO) as a leading alternative technology to the baseline aggregation approach. Over 75 technologies/ideas were evaluated overall. Forty-one technologies/ideas passed the initial screening evaluation. The 41 technologies/ideas were then combined to 16 complete solutions for the disposition of TPB and evaluated in detail. Wet Air Oxidation (WAO) is an aqueous phase process in which soluble or suspended waste components are oxidized using molecular oxygen contained in air. The process operates at elevated temperatures and pressures ranging from 150 to 320 C and 7 to 210 atmospheres, respectively. The products of the reaction are CO{sub 2}, H{sub 2}O, and low molecular weight oxygenated organics (e.g. acetate, oxalate). The basic flow scheme for a typical WAO system is as follows. The waste solution or slurry is pumped through a high-pressure feed pump. An air stream containing sufficient oxygen to meet the oxygen requirements of the waste stream is

  18. Assessment of the impact of oxidation processes on indoor air pollution using the new time-resolved INCA-Indoor model

    NASA Astrophysics Data System (ADS)

    Mendez, Maxence; Blond, Nadège; Blondeau, Patrice; Schoemaecker, Coralie; Hauglustaine, Didier A.

    2015-12-01

    INCA-Indoor, a new indoor air quality (IAQ) model, has been developed to simulate the concentrations of volatile organic compounds (VOC) and oxidants considering indoor air specific processes such as: emission, ventilation, surface interactions (sorption, deposition, uptake). Based on the detailed version of SAPRC-07 chemical mechanism, INCA-Indoor is able to analyze the contribution of the production and loss pathways of key chemical species (VOCs, oxidants, radical species). The potential of this model has been tested through three complementary analyses: a comparison with the most detailed IAQ model found in the literature, focusing on oxidant species; realistic scenarios covering a large range of conditions, involving variable OH sources like HONO; and the investigation of alkenes ozonolysis under a large range of indoor conditions that can increase OH and HO2 concentrations. Simulations have been run changing nitrous acid (HONO) concentrations, NOx levels, photolysis rates and ventilation rates, showing that HONO can be the main source of indoor OH. Cleaning events using products containing D-limonene have been simulated at different periods of the day. These scenarios show that HOX concentrations can significantly increase in specific conditions. An assessment of the impact of indoor chemistry on the potential formation of secondary species such as formaldehyde (HCHO) and acetaldehyde (CH3CHO) has been carried out under various room configuration scenarios and a study of the HOx budget for different realistic scenarios has been performed. It has been shown that, under the simulation conditions, formaldehyde can be affected by oxidant concentrations via chemical production which can account for more than 10% of the total production, representing 6.5 ppb/h. On the other hand, acetaldehyde production is affected more by oxidation processes. When the photolysis rates are high, chemical processes are responsible for about 50% of the total production of

  19. PROJECT WORK PLAN FOR REVISED AIR QUALITY CRITERIA FOR OZONE AND RELATED PHOTOCHEMICAL OXIDANTS (CASAC REVIEW DRAFT)

    EPA Science Inventory

    The U.S. Environmental Protection Agency (EPA) promulgates the National Ambient Air Quality Standards (NAAQS) on the basis of scientific information contained in criteria documents. The previous ozone (O3) criteria document, Air Quality Criteria for Ozone and Related Phot...

  20. PROJECT WORK PLAN FOR REVISED AIR QUALITY CRITERIA FOR OZONE AND RELATED PHOTOCHEMICAL OXIDANTS (EXTERNAL REVIEW DRAFT)

    EPA Science Inventory

    The U.S. Environmental Protection Agency (EPA) promulgates the National Ambient Air Quality Standards (NAAQS) on the basis of scientific information contained in criteria documents. The previous ozone (O3 ) criteria document, Air Quality Criteria for Ozone and Related Photochemi...

  1. Short-Term Oxidation Studies on Nicrofer-6025HT in Air at Elevated Temperatures for Advanced Coal Based Power Plants

    SciTech Connect

    Joshi, Vineet; Meier, Alan M.; Darsell, Jens T.; Nachimuthu, Ponnusamy; Bowden, Mark; Weil, K. Scott

    2013-01-26

    Isothermal oxidation studies were conducted on Nicrofer-6025HT alloy in the temperature range of 700°C to 900°C up to 24 hours. Surface analysis using SEM revealed that the growth of chromia occurred along the grain and twin boundaries. The surface also contained reactive element oxides along the twin and grain boundaries. XRD analysis of the oxide scale indicated the presence of Al2O3, Cr2O3 and NiCr2O4. Cross sectional SEM analysis revealed a composite oxide scale formation on Nicrofer-6025HT, consisting of an outer rich chromia scale and an inner oxide scale of alumina. Traces of titanium and silicon were also identified in the oxide scale while NiCr2O4 spinel phase was located at the interface for the longer times at high temperatures evaluated. Establishment of compact layer of Cr2O3 resulted in a decrease in its own thickening rate but accelerated the formation of Al2O3 at the interface. XPS analysis revealed the presence of iron oxide and nickel oxide in minor quantities on the oxide surface.

  2. Cobaltite oxide nanosheets anchored graphene nanocomposite as an efficient oxygen reduction reaction (ORR) catalyst for the application of lithium-air batteries

    NASA Astrophysics Data System (ADS)

    Gnana kumar, G.; Christy, Maria; Jang, Hosaeng; Nahm, Kee Suk

    2015-08-01

    The graphene/cubic cobaltite oxide nanosheets (rGO/Co3O4) with a face centered cubic crystalline structure are synthesized and are exploited as effective cathode catalysts in high performance Lithium-air batteries. The morphological images enunciate that 220 nm average diameter of Co3O4 nanosheets are effectively anchored over the graphene sheets and the diameter of individual nanoparticles that construct the cubic nanosheets is 5 nm. The growth and composite formation mechanisms of prepared nanostructures are identified from Raman and FT-IR spectroscopic techniques. rGO/Co3O4 composite exhibits a lower voltage, high discharge capacity of 4150 mAh g-1 and displays superior cyclability without any capacity losses, signifying the excellent rechargeability of the fabricated electrodes. The post mortem analysis of electrodes specify the existence of lithium peroxide (Li2O2), lithium oxide (Li2O) and lithium carbonate (Li2CO3) discharge products, revealing the involved electrochemical reaction of Lithium-air batteries. The excellent electrochemical properties of rGO/Co3O4 composite is due to the combination of rapid electrokinetics of electron transport and high electrocatalytic activity toward oxygen reduction reaction given via the synergetic effects of rGO and cubic Co3O4 nanosheets. These findings provide fundamental knowledge on understanding the influence of morphological and structural properties of graphene based nanostructures toward Lithium-air battery performances.

  3. Benefits and technological challenges in the implementation of TiO2-based ultraviolet photocatalytic oxidation (UVPCO) air cleaners

    SciTech Connect

    Hodgson, Al; Destaillats, Hugo; Hotchi, Toshifumi; Fisk, William J.

    2008-10-01

    Heating, ventilating, and cooling classrooms in California consume substantial electrical energy. Indoor air quality (IAQ) in classrooms affects student health and performance. In addition to airborne pollutants that are emitted directly by indoor sources and those generated outdoors, secondary pollutants can be formed indoors by chemical reaction of ozone with other chemicals and materials. Filters are used in nearly all classroom heating, ventilation and air-conditioning (HVAC) systems to maintain energy-efficient HVAC performance and improve indoor air quality; however, recent evidence indicates that ozone reactions with filters may, in fact, be a source of secondary pollutants. This project quantitatively evaluated ozone deposition in HVAC filters and byproduct formation, and provided a preliminary assessment of the extent to which filter systems are degrading indoor air quality. The preliminary information obtained will contribute to the design of subsequent research efforts and the identification of energy efficient solutions that improve indoor air quality in classrooms and the health and performance of students.

  4. AIR POLLUTION CONTROL TECHNOLOGIES

    EPA Science Inventory

    This is a chapter for John Wiley & Son's Mechanical Engineers' Handbook, and covers issues involving air pollution control. Various technologies for controlling sulfur oxides is considered including fuel desulfurization. It also considers control of nitrogen oxides including post...

  5. Volatile organic compound conversion by ozone, hydroxyl radicals, and nitrate radicals in residential indoor air: Magnitudes and impacts of oxidant sources

    NASA Astrophysics Data System (ADS)

    Waring, Michael S.; Wells, J. Raymond

    2015-04-01

    Indoor chemistry may be initiated by reactions of ozone (O3), the hydroxyl radical (OH), or the nitrate radical (NO3) with volatile organic compounds (VOC). The principal indoor source of O3 is air exchange, while OH and NO3 formation are considered as primarily from O3 reactions with alkenes and nitrogen dioxide (NO2), respectively. Herein, we used time-averaged models for residences to predict O3, OH, and NO3 concentrations and their impacts on conversion of typical residential VOC profiles, within a Monte Carlo framework that varied inputs probabilistically. We accounted for established oxidant sources, as well as explored the importance of two newly realized indoor sources: (i) the photolysis of nitrous acid (HONO) indoors to generate OH and (ii) the reaction of stabilized Criegee intermediates (SCI) with NO2 to generate NO3. We found total VOC conversion to be dominated by reactions both with O3, which almost solely reacted with D-limonene, and also with OH, which reacted with D-limonene, other terpenes, alcohols, aldehydes, and aromatics. VOC oxidation rates increased with air exchange, outdoor O3, NO2 and D-limonene sources, and indoor photolysis rates; and they decreased with O3 deposition and nitric oxide (NO) sources. Photolysis was a strong OH formation mechanism for high NO, NO2, and HONO settings, but SCI/NO2 reactions weakly generated NO3 except for only a few cases.

  6. Volatile organic compound conversion by ozone, hydroxyl radicals, and nitrate radicals in residential indoor air: Magnitudes and impacts of oxidant sources

    PubMed Central

    Waring, Michael S.; Wells, J. Raymond

    2016-01-01

    Indoor chemistry may be initiated by reactions of ozone (O3), the hydroxyl radical (OH), or the nitrate radical (NO3) with volatile organic compounds (VOC). The principal indoor source of O3 is air exchange, while OH and NO3 formation are considered as primarily from O3 reactions with alkenes and nitrogen dioxide (NO2), respectively. Herein, we used time-averaged models for residences to predict O3, OH, and NO3 concentrations and their impacts on conversion of typical residential VOC profiles, within a Monte Carlo framework that varied inputs probabilistically. We accounted for established oxidant sources, as well as explored the importance of two newly realized indoor sources: (i) the photolysis of nitrous acid (HONO) indoors to generate OH and (ii) the reaction of stabilized Criegee intermediates (SCI) with NO2 to generate NO3. We found total VOC conversion to be dominated by reactions both with O3, which almost solely reacted with d-limonene, and also with OH, which reacted with d-limonene, other terpenes, alcohols, aldehydes, and aromatics. VOC oxidation rates increased with air exchange, outdoor O3, NO2 and d-limonene sources, and indoor photolysis rates; and they decreased with O3 deposition and nitric oxide (NO) sources. Photolysis was a strong OH formation mechanism for high NO, NO2, and HONO settings, but SCI/NO2 reactions weakly generated NO3 except for only a few cases. PMID:26855604

  7. Synthesis of free-standing carbon nanohybrid by directly growing carbon nanotubes on air-sprayed graphene oxide paper and its application in supercapacitor

    SciTech Connect

    Wei, Li; Jiang, Wenchao; Yuan, Yang; Goh, Kunli; Yu, Dingshan; Wang, Liang; Chen, Yuan

    2015-04-15

    We report the synthesis of a free-standing two dimensional carbon nanotube (CNT)-reduced graphene oxide (rGO) hybrid by directly growing CNTs on air-sprayed GO paper. As a result of the good integration between CNTs and thermally reduced GO film during chemical vapor deposition, excellent electrical conductivity (2.6×10{sup 4} S/m), mechanical flexibility (electrical resistance only increases 1.1% after bent to 90° for 500 times) and a relatively large surface area (335.3 m{sup 2}/g) are achieved. Two-electrode supercapacitor assembled using the CNT–rGO hybrids in ionic liquid electrolyte (1-ethyl-3-methylimidazolium tetrafluoroborate) shows excellent stability upon 500 bending cycles with the gravimetric energy density measuring 23.7 Wh/kg and a power density of 2.0 kW/kg. Furthermore, it shows an impedance phase angle of −64.4° at a frequency of 120 Hz, suggesting good potentials for 120 Hz alternating current line filtering applications. - Graphical abstract: Flexible and highly conductive carbon nanotube-reduced graphene oxide nanohybrid. - Highlights: • Direct growth of carbon nanotubes by chemical vapor deposition on air-sprayed graphene oxide paper. • Two-dimensional carbon nanohybrid with excellent conductivity and mechanical flexibility. • Supercapacitor with excellent performance stability upon mechanical deformation for flexible electronics applications. • Supercapacitor with high impedance phase angle for 120 Hz alternating current line filtering applications.

  8. Electrocatalytic performances of LaNi1-xMgxO3 perovskite oxides as bi-functional catalysts for lithium air batteries

    NASA Astrophysics Data System (ADS)

    Du, Zhenzhen; Yang, Peng; Wang, Long; Lu, Yuhao; Goodenough, J. B.; Zhang, Jian; Zhang, Dawei

    2014-11-01

    Mg-doped perovskite oxides LaNi1-xMgxO3 (x = 0, 0.08, 0.15) electrocatalysts are synthesized by a sol-gel method using citric acid as complex agent and ethylene glycol as thickening agent. The intrinsic oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) activity of as-prepared perovskite oxides in aqueous electrolyte are examined on a rotating disk electrode (RDE) set up. Li-air primary batteries on the basis of Mg-doped perovskite oxides LaNi1-xMgxO3 (x = 0, 0.08, 0.15) and nonaqueous electrolyte are also fabricated and tested. In terms of the ORR current densities and OER current densities, the performance is enhanced in the order of LaNiO3, LaNi0.92Mg0.08O3 and LaNi0.85Mg0.15O3. Most notably, partially substituting nickel with magnesium suppresses formation of Ni2+ and ensures high concentration of both OER and ORR reaction energy favorable Ni3+ (eg = 1) on the surface of perovskite catalysts. Nonaqueous Li-air primary battery using LaNi0.92Mg0.08O3 and LaNi0.85Mg0.15O3 as the cathode catalysts exhibit improved performances compared with LaNiO3 catalyst, which are consistent with the ORR current densities.

  9. Enhanced effect of water vapor on complete oxidation of formaldehyde in air with ozone over MnOx catalysts at room temperature.

    PubMed

    Zhao, De-Zhi; Shi, Chuan; Li, Xiao-Song; Zhu, Ai-Min; Jang, Ben W-L

    2012-11-15

    At room temperature, the enhanced effect of water vapor on ozone catalytic oxidation (OZCO) of formaldehyde to CO2 over MnOx catalysts and the reaction stability was reported. In a dry air stream, only below 20% of formaldehyde could be oxidized into CO2 by O3. In humid air streams (RH≥55%), ∼100% of formaldehyde were oxidized into CO2 by O3 and the reaction stability was significantly enhanced. Meanwhile, in situ Diffuse Reflectance Infrared Fourier Transform (DRIFT) spectra of OZCO of HCHO demonstrate that the amount of both monodentate and bidentate carbonate species on MnOx, in the dry stream, increased gradually with time on stream (TOS). However, in the humid stream, almost no accumulation of carbonate species on the catalysts was observed. To clarify the enhanced mechanism, formaldehyde surface reactions and CO2 adsorption/desorption on the fresh, O3 and O3+H2O treated MnOx catalysts were examined comparatively. PMID:23021101

  10. A simple way to obtain high saturation magnetization for superparamagnetic iron oxide nanoparticles synthesized in air atmosphere: Optimization by experimental design

    NASA Astrophysics Data System (ADS)

    Karaagac, Oznur; Kockar, Hakan

    2016-07-01

    Orthogonal design technique was applied to obtain superparamagnetic iron oxide nanoparticles with high saturation magnetization, Ms. Synthesis of the nanoparticles were done in air atmosphere according to the orthogonal table L934. Magnetic properties of the synthesized nanoparticles were measured by a vibrating sample magnetometer. Structural analysis of the nanoparticles was also carried out by X-ray diffraction technique (XRD), Fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). After the analysis of magnetic data, the optimized experimental parameters were determined as [Fe+2]/[Fe+3]=6/6, iron ion concentration=1500 mM, base concentration=6.7 M and reaction time=2 min. Magnetic results showed that the synthesis carried out according to the optimized conditions gave the highest Ms of 69.83 emu/g for the nanoparticles synthesized in air atmosphere. Magnetic measurements at 10 K and 300 K showed the sample is superparamagnetic at room temperature. Structural analysis by XRD, FTIR and selected area electron diffraction showed that the sample had the inverse spinel crystal structure of iron oxide. The particle size of the optimized sample determined from the TEM image is 7.0±2.2 nm. The results indicated that the Ms of superparamagnetic iron oxide nanoparticles can be optimized by experimental design with the suitable choice of the synthesis parameters.

  11. Real-time measurements of secondary organic aerosol formation and aging from ambient air in an oxidation flow reactor in the Los Angeles area

    NASA Astrophysics Data System (ADS)

    Ortega, A. M.; Hayes, P. L.; Peng, Z.; Palm, B. B.; Hu, W.; Day, D. A.; Li, R.; Cubison, M. J.; Brune, W. H.; Graus, M.; Warneke, C.; Gilman, J. B.; Kuster, W. C.; de Gouw, J. A.; Jimenez, J. L.

    2015-08-01

    Field studies in polluted areas over the last decade have observed large formation of secondary organic aerosol (SOA) that is often poorly captured by models. The study of SOA formation using ambient data is often confounded by the effects of advection, vertical mixing, emissions, and variable degrees of photochemical aging. An Oxidation Flow Reactor (OFR) was deployed to study SOA formation in real-time during the CalNex campaign in Pasadena, CA, in 2010. A high-resolution aerosol mass spectrometer (AMS) and a scanning mobility particle sizer (SMPS) alternated sampling ambient and reactor-aged air. The reactor produced OH concentrations up to 4 orders of magnitude higher than in ambient air, achieving equivalent atmospheric aging from hours up to several weeks in 3 min of processing. OH radical concentration was continuously stepped, obtaining measurements of real-time SOA formation and oxidation at multiple equivalent ages from 0.8 days-6.4 weeks. Enhancement of OA from aging showed a maximum net SOA production between 0.8-6 days of aging with net OA mass loss beyond 2 weeks. Reactor SOA mass peaked at night, in the absence of ambient photochemistry, and correlated with trimethylbenzene concentrations. Reactor SOA formation was inversely correlated with ambient SOA and Ox, which along with the short-lived VOC correlation, indicates the importance of relatively reactive (τOH ∼ 0.3 day) SOA precursors in the LA-Basin. Evolution of the elemental composition in the reactor was similar to trends observed in the atmosphere (O : C vs. H : C slope ∼ -0.65). Oxidation state of carbon (OSC) in reactor SOA increased steeply with age and remained elevated (OSC ∼ 2) at the highest photochemical ages probed. The ratio of OA in the reactor output to excess CO (ΔCO, ambient CO above regional background) vs. photochemical age is similar to previous studies at low to moderate ages and also extends to higher ages where OA loss dominates. The mass added at low

  12. Oxalate-assisted oxidative degradation of 4-chlorophenol in a bimetallic, zero-valent iron-aluminum/air/water system.

    PubMed

    Fan, Jinhong; Wang, Hongwu; Ma, Luming

    2016-08-01

    The reaction of zero-valent iron and aluminum with oxygen produced reactive oxidants that can oxidize 4-chlorophenol (4-CP). However, oxidant yield without metal surface cleaning to dissolve the native oxide layer or in the absence of ligands was too low for practical applications. The addition of oxalate (ox) to dissolved oxygen-saturated solution of Fe(0)-Al(0) significantly increased oxidant yield because of the dissolution, pH buffer, and complexing characteristics of ox. Ox-enhanced reactive oxidant generation was affected by ox concentration and solution pH. The critical effect of ox dosing was confirmed with the reactive species of [Fe(II)(ox)0] and [Fe(II)(ox)2 (2-)]. Systematic studies on the effect of the initial and in situ solution pH revealed that 4-CP oxidation was controlled by the continuous release of dissolved Fe(2+) and Al(3+), their fate, and the activation mechanisms of O2 reduction. The degradation pathway of 4-CP in ox-enhanced Fe(0)-Al(0)/O2 may follow the 4-chlorocatechol pathway. The robustness of the ox-enhanced Al(0)-Fe(0)-O2 process was determined with one-time dosing of ox. Therefore, ox is an ideal additive to enhancing the Fe(0)-Al(0)/O2 system for the oxidative degradation of aqueous organic pollutants. PMID:27180839

  13. In vitro comparative bond strength of contemporary self-adhesive resin cements to zirconium oxide ceramic with and without air-particle abrasion.

    PubMed

    Blatz, Markus B; Phark, Jin-Ho; Ozer, Fusun; Mante, Francis K; Saleh, Najeed; Bergler, Michael; Sadan, Avishai

    2010-04-01

    This study compared shear bond strengths of six self-adhesive resin cements to zirconium oxide ceramic with and without air-particle abrasion. One hundred twenty zirconia samples were air-abraded (group SB; n = 60) or left untreated (group NO). Composite cylinders were bonded to the zirconia samples with either BisCem (BC), Maxcem (MC), G-Cem (GC), RelyX Unicem Clicker (RUC), RelyX Unicem Applicator (RUA), or Clearfil SA Cement (CSA). Shear bond strength was tested after thermocycling, and data were analyzed with analysis of variance and Holm-Sidak pairwise comparisons. Without abrasion, RUA (8.0 MPa), GC (7.9 MPa), and CSA (7.6 MPa) revealed significantly higher bond strengths than the other cements. Air-particle abrasion increased bond strengths for all test cements (p < 0.001). GC (22.4 MPa) and CSA (18.4 MPa) revealed the highest bond strengths in group SB. Bond strengths of self-adhesive resin cements to zirconia were increased by air-particle abrasion. Cements containing adhesive monomers (MDP/4-META) were superior to other compositions. PMID:19415350

  14. Solving widespread low-concentration VOC air pollution problems: Gas-phase photocatalytic oxidation answers the needs of many small businesses

    SciTech Connect

    Lyons, C; Turchi, C; Gratson, D

    1995-04-01

    Many small businesses are facing new regulations under the 1990 Amendments to the Clean Air Act. Regulators, as well as the businesses themselves, face new challenges to control small point-source air pollution emissions. An individual business-such as a dry cleaner, auto repair shop, bakery, coffee roaster, photo print shop, or chemical company-may be an insignificant source of air pollution, but collectively, the industry becomes a noticeable source. Often the businesses are not equipped to respond to new regulatory requirements because of limited resources, experience, and expertise. Also, existing control strategies may be inappropriate for these businesses, having been developed for major industries with high volumes, high pollutant concentrations, and substantial corporate resources. Gas-phase photocatalytic oxidation (PCO) is an option for eliminating low-concentration, low-flow-rate emissions of volatile organic compounds (VOCs) from small business point sources. The advantages PCO has over other treatment techniques are presented in this paper. This paper also describes how PCO can be applied to specific air pollution problems. We present our methodology for identifying pollution problems for which PCO is applicable and for reaching the technology`s potential end users. PCO is compared to other gas-phase VOC control technologies.

  15. Effects of Thermal Cycling and Thermal Aging on the Hermeticity and Strength of Silver-Copper Oxide Air-Brazed Seals

    SciTech Connect

    Weil, K. Scott; Coyle, Christopher A.; Darsell, Jens T.; Xia, Gordon; Hardy, John S.

    2005-12-01

    Thermal cycle and exposure tests were conducted on ceramic-to-metal joints prepared by a new sealing technique. Known as reactive air brazing, this joining method is currently being considered for use in sealing various high-temperature solid-state electrochemical devices, including planar solid oxide fuel cells (pSOFC). In order to simulate a typical pSOFC application, test specimens were prepared by joining ceramic anode/electrolyte bilayers to washers, of the same composition as the common frame materials employed in pSOFC stacks, using a filler metal composed of 4mol% CuO in silver. The brazed samples were exposure tested at 750°C for 200, 400, and 800hrs in both simulated fuel and air environments and thermally cycled at rapid rate (75°C/min) between room temperature and 750°C for as many as fifty cycles. Subsequent joint strength testing and microstructural analysis indicated that the samples exposure tested in air displayed little degradation with respect to strength, hermeticity, or microstructure out to 800hrs of exposure. Those tested in fuel showed no change in rupture strength or loss in hermeticity after 800hrs of high-temperature exposure, but did undergo microstructural change due to the dissolution of hydrogen into the silver-based braze material. Air brazed specimens subjected to rapid thermal cycling exhibited no loss in joint strength or hermeticity, but displayed initial signs of seal delamination along the braze/electrolyte interface after 50 cycles.

  16. Simulating secondary organic aerosol in a regional air quality model using the statistical oxidation model - Part 1: Assessing the influence of constrained multi-generational ageing

    NASA Astrophysics Data System (ADS)

    Jathar, S. H.; Cappa, C. D.; Wexler, A. S.; Seinfeld, J. H.; Kleeman, M. J.

    2016-02-01

    Multi-generational oxidation of volatile organic compound (VOC) oxidation products can significantly alter the mass, chemical composition and properties of secondary organic aerosol (SOA) compared to calculations that consider only the first few generations of oxidation reactions. However, the most commonly used state-of-the-science schemes in 3-D regional or global models that account for multi-generational oxidation (1) consider only functionalization reactions but do not consider fragmentation reactions, (2) have not been constrained to experimental data and (3) are added on top of existing parameterizations. The incomplete description of multi-generational oxidation in these models has the potential to bias source apportionment and control calculations for SOA. In this work, we used the statistical oxidation model (SOM) of Cappa and Wilson (2012), constrained by experimental laboratory chamber data, to evaluate the regional implications of multi-generational oxidation considering both functionalization and fragmentation reactions. SOM was implemented into the regional University of California at Davis / California Institute of Technology (UCD/CIT) air quality model and applied to air quality episodes in California and the eastern USA. The mass, composition and properties of SOA predicted using SOM were compared to SOA predictions generated by a traditional two-product model to fully investigate the impact of explicit and self-consistent accounting of multi-generational oxidation.Results show that SOA mass concentrations predicted by the UCD/CIT-SOM model are very similar to those predicted by a two-product model when both models use parameters that are derived from the same chamber data. Since the two-product model does not explicitly resolve multi-generational oxidation reactions, this finding suggests that the chamber data used to parameterize the models captures the majority of the SOA mass formation from multi-generational oxidation under the conditions

  17. From ketones to esters by a Cu-catalyzed highly selective C(CO)-C(alkyl) bond cleavage: aerobic oxidation and oxygenation with air.

    PubMed

    Huang, Xiaoqiang; Li, Xinyao; Zou, Miancheng; Song, Song; Tang, Conghui; Yuan, Yizhi; Jiao, Ning

    2014-10-22

    The Cu-catalyzed aerobic oxidative esterification of simple ketones via C-C bond cleavage has been developed. Varieties of common ketones, even inactive aryl long-chain alkyl ketones, are selectively converted into esters. The reaction tolerates a wide range of alcohols, including primary and secondary alcohols, chiral alcohols with retention of the configuration, electron-deficient phenols, as well as various natural alcohols. The usage of inexpensive copper catalyst, broad substrate scope, and neutral and open air conditions make this protocol very practical. (18)O labeling experiments reveal that oxygenation occurs during this transformation. Preliminary mechanism studies indicate that two novel pathways are mainly involved in this process. PMID:25251943

  18. Ligand-free Cu-catalyzed [3 + 2] cyclization for the synthesis of pyrrolo[1,2-a]quinolines with ambient air as a terminal oxidant.

    PubMed

    Yu, Yang; Liu, Yuan; Liu, Aoxia; Xie, Hexin; Li, Hao; Wang, Wei

    2016-08-21

    A ligand-free Cu-catalyzed [3 + 2] cycloaddition of ethyl 2-(quinolin-2-yl)acetates, ethyl 2-(isoquinolin-1-yl)acetates, and ethyl 2-(pyridin-2-yl)acetates with (E)-chalcones for a "one-pot" synthesis of pyrrolo[1,2-a]quinolines, pyrrolo[2,1-a]isoquinolines and indolizines has been developed. The annulation products were isolated in moderate to good yields with air as the sole oxidant under mild conditions. PMID:27452813

  19. The double perovskite oxide Sr2CrMoO(6-δ) as an efficient electrocatalyst for rechargeable lithium air batteries.

    PubMed

    Ma, Zhong; Yuan, Xianxia; Li, Lin; Ma, Zi-Feng

    2014-12-01

    A double perovskite oxide Sr2CrMoO6-δ (SCM), synthesized using the sol-gel and annealing method with the assistance of citric acid and ethylene diamine tetraacetic acid, was investigated for the first time as an efficient catalyst for rechargeable lithium air batteries. The SCM cathode enables higher specific capacity, lower overpotential and a much better cyclability compared to the pure Super P electrode owing to its excellent electrocatalytic activity towards the formation/decomposition of Li2O2. PMID:25325080

  20. Effect of nitric oxide on photochemical ozone formation in mixtures of air with molecular chlorine and with trichlorofluoromethane

    NASA Technical Reports Server (NTRS)

    Bittker, D. A.; Wong, E. L.

    1978-01-01

    Ozone formation in a reaction chamber at room temperature and atmospheric pressure were studied for the photolysis of mixtures of NO with either Cl2 or CFCl3 in air. Both Cl2 + NO and CFCl3 + NO in air strongly inhibited O3 formation during the entire 3 to 4 hour reaction. A chemical mechanism that explains the results was presented. An important part of this mechanism was the formation and destruction of chlorine nitrate. Computations were performed with this same mechanism for CFCl3-NO-air mixtures at stratospheric temperatures, pressures, and concentrations. Results showed large reductions in steady-state O3 concentrations in these mixtures as compared with pure air.

  1. Evaluation of Ultra-Violet Photocatalytic Oxidation (UVPCO) forIndoor Air Applications: Conversion of Volatile Organic Compounds at LowPart-per-Billion Concentrations

    SciTech Connect

    Hodgson, Alfred T.; Sullivan, Douglas P.; Fisk, William J.

    2005-09-30

    Efficient removal of indoor generated airborne particles and volatile organic compounds (VOCs) in office buildings and other large buildings may allow for a reduction in outdoor air supply rates with concomitant energy savings while still maintaining acceptable indoor air quality in these buildings. Ultra-Violet Photocatalytic Oxidation (UVPCO) air cleaners have the potential to achieve the necessary reductions in indoor VOC concentrations at relatively low cost. In this study, laboratory experiments were conducted with a scaled, prototype UVPCO device designed for use in a duct system. The experimental UVPCO contained two 30 by 30-cm honeycomb monoliths coated with titanium dioxide and 3% by weight tungsten oxide. The monoliths were irradiated with 12 UVC lamps arranged in four banks. The UVPCO was challenged with four mixtures of VOCs typical of mixtures encountered in indoor air. A synthetic office mixture contained 27 VOCs commonly measured in office buildings. A cleaning product mixture contained three cleaning products with high market shares. A building product mixture was created by combining sources including painted wallboard, composite wood products, carpet systems, and vinyl flooring. A fourth mixture contained formaldehyde and acetaldehyde. Steady-state concentrations were produced in a classroom laboratory or a 20-m{sup 3} environmental chamber. Air was drawn through the UVPCO, and single pass conversion efficiencies were measured from replicate air samples collected upstream and downstream of the reactor section. Concentrations of the mixtures were manipulated, with concentrations of individual VOCs mostly maintained below 10 ppb. Device flow rates were varied between 165 and 580 m{sup 3}/h. Production of formaldehyde, acetaldehyde, acetone, formic acid, and acetic acid as reaction products was investigated. Conversion efficiency data were generated for 48 individual VOCs or groups of closely related compounds. Alcohols and glycol ethers were the

  2. Magnetron sputtered Si-B-C-N films with high oxidation resistance and thermal stability in air at temperatures above 1500 deg. C

    SciTech Connect

    Vlcek, Jaroslav; Hreben, Stanislav; Kalas, Jiri; Capek, Jiri; Zeman, Petr; Cerstvy, Radomir; Perina, Vratislav; Setsuhara, Yuichi

    2008-09-15

    Novel quaternary Si-B-C-N materials are becoming increasingly attractive because of their possible high-temperature and harsh-environment applications. In the present work, amorphous Si-B-C-N films were deposited on Si and SiC substrates by reactive dc magnetron cosputtering using a single C-Si-B or B{sub 4}C-Si target in nitrogen-argon gas mixtures. A fixed 75% Si fraction in the target erosion areas, a rf induced negative substrate bias voltage of -100 V, a substrate temperature of 350 deg. C, and a total pressure of 0.5 Pa were used in the depositions. The corresponding discharge and deposition characteristics (such as the ion-to-film-forming particle flux ratio, ion energy per deposited atom, and deposition rate) are presented to understand complex relationships between process parameters and film characteristics. Films deposited under optimized conditions (B{sub 4}C-Si target, 50% N{sub 2}+50% Ar gas mixture), possessing a composition (in at. %) Si{sub 32-34}B{sub 9-10}C{sub 2-4}N{sub 49-51} with a low (less than 5 at. %) total content of hydrogen and oxygen, exhibited extremely high oxidation resistance in air at elevated temperatures (even above 1500 deg. C). Formation of protective surface layers (mainly composed of Si and O) was proved by high-resolution transmission electron microscopy, Rutherford backscattering spectrometry, and x-ray diffraction measurements after oxidization. Amorphous structure of the Si-B-C-N films was maintained under the oxidized surface layers after annealing in air up to 1700 deg. C (a limit imposed by thermogravimetric analysis in oxidative atmospheres)

  3. No oxidative stress or DNA damage in peripheral blood mononuclear cells after exposure to particles from urban street air in overweight elderly

    PubMed Central

    Hemmingsen, Jette Gjerke; Jantzen, Kim; Møller, Peter; Loft, Steffen

    2015-01-01

    Exposure to traffic-related particulate matter (PM) has been associated with increased risk of lung disease, cancer and cardiovascular disease especially in elderly and overweight subjects. The proposed mechanisms involve intracellular production of reactive oxygen species (ROS), inflammation and oxidation-induced DNA damage studied mainly in young normal-weight subjects. We performed a controlled cross-over, randomised, single-blinded, repeated-measure study where 60 healthy subjects (25 males and 35 females) with age 55–83 years and body mass index above 25kg/m2 were exposed for 5h to either particle-filtered or sham-filtered air from a busy street with number of concentrations and PM2.5 levels of 1800/cm3 versus 23 000/cm3 and 3 µg/m3 versus 24 µg/m3, respectively. Peripheral blood mononuclear cells (PBMCs) were collected and assayed for production of ROS with and without ex vivo exposure to nanosized carbon black as well as expression of genes related to inflammation (chemokine (C-C motif) ligand 2, interleukin-8 and tumour necrosis factor), oxidative stress response (heme oxygenase (decycling)-1) and DNA repair (oxoguanine DNA glycosylase). DNA strand breaks and oxidised purines were assayed by the alkaline comet assay. No statistically significant differences were found for any biomarker immediately after exposure to PM from urban street air although strand breaks and oxidised purines combined were significantly associated with the particle number concentration during exposure. In conclusion, 5h of controlled exposure to PM from urban traffic did not change the gene expression related to inflammation, oxidative stress or DNA repair, ROS production or oxidatively damaged DNA in PBMCs from elderly overweight human subjects. PMID:25904586

  4. No oxidative stress or DNA damage in peripheral blood mononuclear cells after exposure to particles from urban street air in overweight elderly.

    PubMed

    Hemmingsen, Jette Gjerke; Jantzen, Kim; Møller, Peter; Loft, Steffen

    2015-09-01

    Exposure to traffic-related particulate matter (PM) has been associated with increased risk of lung disease, cancer and cardiovascular disease especially in elderly and overweight subjects. The proposed mechanisms involve intracellular production of reactive oxygen species (ROS), inflammation and oxidation-induced DNA damage studied mainly in young normal-weight subjects. We performed a controlled cross-over, randomised, single-blinded, repeated-measure study where 60 healthy subjects (25 males and 35 females) with age 55-83 years and body mass index above 25 kg/m(2) were exposed for 5h to either particle-filtered or sham-filtered air from a busy street with number of concentrations and PM2.5 levels of 1800/cm(3) versus 23 000/cm(3) and 3 µg/m(3) versus 24 µg/m(3), respectively. Peripheral blood mononuclear cells (PBMCs) were collected and assayed for production of ROS with and without ex vivo exposure to nanosized carbon black as well as expression of genes related to inflammation (chemokine (C-C motif) ligand 2, interleukin-8 and tumour necrosis factor), oxidative stress response (heme oxygenase (decycling)-1) and DNA repair (oxoguanine DNA glycosylase). DNA strand breaks and oxidised purines were assayed by the alkaline comet assay. No statistically significant differences were found for any biomarker immediately after exposure to PM from urban street air although strand breaks and oxidised purines combined were significantly associated with the particle number concentration during exposure. In conclusion, 5h of controlled exposure to PM from urban traffic did not change the gene expression related to inflammation, oxidative stress or DNA repair, ROS production or oxidatively damaged DNA in PBMCs from elderly overweight human subjects. PMID:25904586

  5. High temperature air oxidation resistance of TiAlCr-Y coated Ti45Al8Nb between 750 °C - 950 °C

    NASA Astrophysics Data System (ADS)

    Dudziak, Tomasz; Datta, Prasanta; Du, Hailiang; Ross, Ian

    2013-12-01

    This study is concerned with air oxidation of TiAlCr-Y coated Ti45Al-8Nb (at%) alloy between 750 °C-950 °C for 500 hours. It was shown in these tests that at 750 °C, 850 °C and 950 °C, the oxidation degradation increased with temperature: at 750 °C the oxide scale consisted of TiO2/Al2O3/Cr2O3 phases, whilst at 850 °C the oxide scale consisted of TiO2/Al2O3 phases with a small amount of Cr2O3, and larger number of voids. The material exposed at 950 °C showed a significant formation of TiO2 with a small amount of Al2O3 and high number of voids; the formation of Cr2O3 at 950 °C was inhibited mainly due to the formation of volatile CrO3 or CrO2(OH)2 phase.

  6. [Photometric method of the detection of magnesium oxide in the working zone air after using magnesium caustic dust].

    PubMed

    Putilina, O N; Makarevskaia, V V

    1991-01-01

    The contributors proposed a new highly sensitive selective technique of magnesium oxide detection, based on the Congo red and salicylic acid reaction. The minimal detection level is 0.25 mg of magnesium oxide in the analyzed sample volume. The range of measured concentrations varies from 0.01 to 0.4 mcg/ml. The express technique is simple and selective with Ca (II), Fe (III), AI (III). PMID:2060814

  7. Designing a Cu(II)-ArCu(II)-ArCu(III)-Cu(I) catalytic cycle: Cu(II)-catalyzed oxidative arene C-H bond azidation with air as an oxidant under ambient conditions.

    PubMed

    Yao, Bo; Liu, Yang; Zhao, Liang; Wang, De-Xian; Wang, Mei-Xiang

    2014-11-21

    On the basis of our recent discovery of high valent organocopper compounds, we have designed and achieved efficient copper(II)-catalyzed oxidative arene C-H bond azidation under very mild aerobic conditions by using NaN3 as an azide source. In the presence of a Cu(II) catalyst, a number of azacalix[1]arene[3]pyridines underwent direct arene C-H bond cupration through an electrophilic aromatic metalation pathway to form an arylcopper(II) intermediate. Oxidized by a free copper(II) ion, the arylcopper(II) intermediate was transformed into an arylcopper(III) species that subsequently cross-coupled with azide to furnish the formation of aryl azide products with the release of a copper(I) ion. Under ambient catalytic reaction conditions, the copper(I) species generated was oxidized by air into copper(II), which entered into the next catalytic cycle. Application of the method was demonstrated by the synthesis of functional azacalix[1]arene[3]pyridines by means of simple and practical functional group transformations of azide. The showcase of the Cu(II)-ArCu(II)-ArCu(III)-Cu(I) catalytic cycle would provide a new strategy for the design of copper(II)-catalyzed aerobic oxidative arene C-H bond activation and transformations. PMID:25350606

  8. Numerical prediction of system round-trip efficiency and feasible operating conditions of small-scale solid oxide iron-air battery

    NASA Astrophysics Data System (ADS)

    Ohmori, Hiroko; Iwai, Hiroshi; Itakura, Kotaro; Saito, Motohiro; Yoshida, Hideo

    2016-03-01

    A simulation model of a small-scale solid oxide iron-air battery system was developed to clarify its fundamental characteristics and feasibility from the view point of energy efficiency. The energy flow in one cycle of charge/discharge operations was evaluated under a quasi-state assumption with 0-dimensional models of the system components, i.e., a solid oxide electrochemical cell, an iron (Fe) box and heat exchangers. Special care was taken when considering thermal aspects; not only a simple system but also a more complicated system with thermal recirculation by three heat exchangers was investigated. It was found that the system round-trip efficiency reaches 61% under the base conditions in this study. The results also show that several limitations exist for the operation parameters and conditions in view of practical applications. In particular, higher and lower limits exist for the fuel and air utilization factors under which the system operates effectively because of constraints such as the maximum allowable fuel-blower temperature and no heat input during the discharge operation.

  9. Removal of organic pollutants from 2,2',5,5'-tetrachlorobenzidine (TCB) industrial wastewater by micro-electrochemical oxidation and air-stripping.

    PubMed

    Shibin, Xia; Shuichun, Xia; Changqing, Zhu

    2007-06-01

    A feasible method for treatment of the wastewater from the two-staged neutralization in 2,2',5,5'-tetrachlorobenzidine (TCB) manufacturing processes, a refractory dye intermediate effluents, based on combined micro-electrochemical oxidation or iron-chipping filtration (ICF) and air-stripping reactor (ASR), was developed. On conditions of HRT 1h, pH 3.0 in ICF and HRT 38 h, gas-liquid ratio 15, pH 6.0-8.65, temperature 26 degrees C in ASR, the overall COD, color, TCB and NH(4)(+)-N removal were 96.8%, 91%, 87.61% and 62%, respectively, during the treatment of TCB wastewater from the two-staged neutralization dissolved by methanol. The averaged 18.3%, 81.7% of the total degraded COD, 35.2%, 64.8% of TCB were carried out in ICF and ASR, respectively. NH(4)(+)-N removal was finished mainly in ASR. The experimental results indicated that the combined micro-electrochemical oxidation and air-stripping process performed good treatment of COD, color, TCB and NH(4)(+)-N removal in TCB wastewater from the two-staged neutralization dissolved by ethanol or acetone, came up the discharge standard in China. But the TCB wastewater from the two-staged neutralization dissolved by methanol should be deeply treated before discharged. PMID:17118553

  10. Integrating NiCo Alloys with Their Oxides as Efficient Bifunctional Cathode Catalysts for Rechargeable Zinc-Air Batteries.

    PubMed

    Liu, Xien; Park, Minjoon; Kim, Min Gyu; Gupta, Shiva; Wu, Gang; Cho, Jaephil

    2015-08-10

    The lack of high-efficient, low-cost, and durable bifunctional electrocatalysts that act simultaneously for the oxygen reduction reaction (ORR) and the oxygen evolution reaction (OER) is currently one of the major obstacles to commercializing the electrical rechargeability of zinc-air batteries. A nanocomposite CoO-NiO-NiCo bifunctional electrocatalyst supported by nitrogen-doped multiwall carbon nanotubes (NCNT/CoO-NiO-NiCo) exhibits excellent activity and stability for the ORR/OER in alkaline media. More importantly, real air cathodes made from the bifunctional NCNT/CoO-NiO-NiCo catalysts further demonstrated superior performance to state-of-the-art Pt/C or Pt/C+IrO2 catalysts in primary and rechargeable zinc-air batteries. PMID:26118973

  11. Effect excess air as an oxidizer in the flame assisted spray dryer using computational fluid dynamics approach

    NASA Astrophysics Data System (ADS)

    Septiani, Eka Lutfi; Widiyastuti, W.; Nurtono, Tantular; Winardi, Sugeng

    2016-02-01

    The size distribution of silica particles as a model material from colloidal silica solution precursor in the flame assisted spray dryer method were studied numerically using Computational Fluid Dynamics (CFD). CFD has ability to solve the momentum, energy and mass transfer equation well. k-ɛ model was used to describe the turbulence model and non-premixed combustion model was used to combustion model. Collision and break-up model were also considered to predict the final particles size distribution. For validation, LPG with flow rate of 0.5 L/minute LPG and 200% excess air were used as energy sources. At this condition, numerical solution agreed well to the experimental work resulting in polydisperse size distribution. Therefore, others excess air, 100% and 150% were also observed using CFD and evaluated their contribution to their particles size distribution. Monodisperse particles size distribution were obtained when the combustion used 150% excess air.

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

    NASA Astrophysics Data System (ADS)

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

    2012-04-01

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

  13. Interfacial redox reaction-directed synthesis of silver@cerium oxide core-shell nanocomposites as catalysts for rechargeable lithium-air batteries

    NASA Astrophysics Data System (ADS)

    Liu, Ying; Wang, Man; Cao, Lu-Jie; Yang, Ming-Yang; Ho-Sum Cheng, Samson; Cao, Chen-Wei; Leung, Kwan-Lan; Chung, Chi-Yuen; Lu, Zhou-Guang

    2015-07-01

    A facile oxidation-reduction reaction method has been implemented to prepare pomegranate-like Ag@CeO2 multicore-shell structured nanocomposites. Under Ar atmosphere, redox reaction automatically occurs between AgNO3 and Ce(NO3)3 in an alkaline solution, where Ag+ is reduced to Ag nanopartilces and Ce3+ is simultaneously oxidized to form CeO2, followed by the self-assembly to form the pomegranate-like multicore-shell structured Ag@CeO2 nanocomposites driven by thermodynamic equilibrium. No other organic amines or surfactants are utilized in the whole reaction system and only NaOH instead of organic reducing agent is used to prevent the introduction of a secondary reducing byproduct. The as-obtained pomegranate-like Ag@CeO2 multicore-shell structured nanocomposites have been characterized as electro-catalysts for the air cathode of lithium-air batteries operated in a simulated air environment. Superior electrochemical performance with high discharge capacity of 3415 mAh g-1 at 100 mA g-1, stable cycling and small charge/discharge polarization voltage is achieved, which is much better than that of the CeO2 or simple mixture of CeO2 and Ag. The enhanced properties can be primarily attributed to the synergy effect between the Ag core and the CeO2 shell resulting from the unique pomegranate-like multicore-shell nanostructures possessing plenty of active sites to promote the facile formation and decomposition of Li2O2.

  14. Simultaneous stripping recovery of ammonia-nitrogen and precipitation of manganese from electrolytic manganese residue by air under calcium oxide assist.

    PubMed

    Chen, Hongliang; Liu, Renlong; Shu, Jiancheng; Li, Wensheng

    2015-01-01

    Leaching tests of electrolytic manganese residue (EMR) indicated that high contents of soluble manganese and ammonia-nitrogen posed a high environmental risk. This work reports the results of simultaneous stripping recovery of ammonia-nitrogen and precipitation of manganese by air under calcium oxide assist. The ammonia-nitrogen stripping rate increased with the dosage of CaO, the air flow rate and the temperature of EMR slurry. Stripped ammonia-nitrogen was absorbed by a solution of sulfuric acid and formed soluble (NH4)2SO4 and (NH4)3H(SO4)3. The major parameters that effected soluble manganese precipitation were the dosage of added CaO and the slurry temperature. Considering these two aspects, the efficient operation conditions should be conducted with 8 wt.% added CaO, 60°C, 800 mL min(-1) air flow rate and 60-min reaction time. Under these conditions 99.99% of the soluble manganese was precipitated as Mn3O4, which was confirmed by XRD and SEM-EDS analyses. In addition, the stripping rate of ammonia-nitrogen was 99.73%. Leaching tests showed the leached toxic substances concentrations of the treated EMR met the integrated wastewater discharge standard of China (GB8978-1996). PMID:26301855

  15. Study on the Catalytic Activity of Noble Metal Nanoparticles on Reduced Graphene Oxide for Oxygen Evolution Reactions in Lithium-Air Batteries.

    PubMed

    Jeong, Yo Sub; Park, Jin-Bum; Jung, Hun-Gi; Kim, Jooho; Luo, Xiangyi; Lu, Jun; Curtiss, Larry; Amine, Khalil; Sun, Yang-Kook; Scrosati, Bruno; Lee, Yun Jung

    2015-07-01

    Among many challenges present in Li-air batteries, one of the main reasons of low efficiency is the high charge overpotential due to the slow oxygen evolution reaction (OER). Here, we present systematic evaluation of Pt, Pd, and Ru nanoparticles supported on rGO as OER electrocatalysts in Li-air cell cathodes with LiCF3SO3-tetra(ethylene glycol) dimethyl ether (TEGDME) salt-electrolyte system. All of the noble metals explored could lower the charge overpotentials, and among them, Ru-rGO hybrids exhibited the most stable cycling performance and the lowest charge overpotentials. Role of Ru nanoparticles in boosting oxidation kinetics of the discharge products were investigated. Apparent behavior of Ru nanoparticles was different from the conventional electrocatalysts that lower activation barrier through electron transfer, because the major contribution of Ru nanoparticles in lowering charge overpotential is to control the nature of the discharge products. Ru nanoparticles facilitated thin film-like or nanoparticulate Li2O2 formation during oxygen reduction reaction (ORR), which decomposes at lower potentials during charge, although the conventional role as electrocatalysts during OER cannot be ruled out. Pt-and Pd-rGO hybrids showed fluctuating potential profiles during the cycling. Although Pt- and Pd-rGO decomposed the electrolyte after electrochemical cycling, no electrolyte instability was observed with Ru-rGO hybrids. This study provides the possibility of screening selective electrocatalysts for Li-air cells while maintaining electrolyte stability. PMID:26115340

  16. Oxidation of UO 2 fuel pellets in air at 503 and 543 K studied using X-ray photoelectron spectroscopy and X-ray diffraction

    NASA Astrophysics Data System (ADS)

    Tempest, P. A.; Tucker, P. M.; Tyler, J. W.

    1988-02-01

    An understanding of the low temperature oxidation behaviour of UO 2 pellets in air is important in the unlikely event of gas ingress to a fuel can during handling or storage. The main parameter of concern is the production time of U 3O 8 particulate as a function of temperature. Factors which affect the UO2 → U3O8 transformation have been investigated by sequentially oxidising UO 2 fuel pellets in air at 503 and 543 K and monitoring the growth of U 3O and U 3O 7 using X-ray photoelectron spectroscopy, X-ray diffraction and scanning electron microscopy. Initially oxidation proceeded at a linear rate by the inward diffusion of oxygen to form a complete layer of substoichiometric U 3O 7. This phase was tetragonal with a {c}/{a} ratio of 1.015, significantly less than the value of 1.03 measured on UO 2 powder when oxidised under identical conditions. This difference and the preferred orientation exhibited by surface grains were caused by growth stresses induced in the pellet surface. Both intergranular and transgranular cracking occurred and became nucleation sites for the growth of U 3O 8. The linear oxidation period associated with U 3O 7 growth was much shorter at 543 than at 503 K and U 3O 8 nucleated earlier. Spallation and the production of particulate were only observed during the formation of U 3O 8 when a 30% increase in volume arose from the U3O7 → U3O8 phase change.

  17. Cycle analysis of an integrated solid oxide fuel cell and recuperative gas turbine with an air reheating system

    NASA Astrophysics Data System (ADS)

    Zhang, Xiongwen; Li, Jun; Li, Guojun; Feng, Zhenping

    Cycle simulation and analysis for two kinds of SOFC/GT hybrid systems were conducted with the help of the simulation tool: Aspen Custom Modeler. Two cycle schemes of recuperative heat exchanger (RHE) and exhaust gas recirculated (EGR) were described according to the air reheating method. The system performance with operating pressure, turbine inlet temperature and fuel cell load were studied based on the simulation results. Then the effects of oxygen utilization, fuel utilization, operating temperature and efficiencies of the gas turbine components on the system performance of the RHE cycle and the EGR cycle were discussed in detail. Simulation results indicated that the system optimum efficiency for the EGR air reheating cycle scheme was higher than that of the RHE cycle system. A higher pressure ratio would be available for the EGR cycle system in comparison with the RHE cycle. It was found that increasing fuel utilization or oxygen utilization would decrease fuel cell efficiency but improve the system efficiency for both of the RHE and EGR cycles. The efficiency of the RHE cycle hybrid system decreased as the fuel cell air inlet temperature increased. However, the system efficiency of EGR cycle increased with fuel cell air inlet temperature. The effect of turbine efficiency on the system efficiency was more obvious than the effect of the compressor and recuperator efficiencies among the gas turbine components. It was also indicated that improving the gas turbine component efficiencies for the RHE cycle increased system efficiency higher than that for the EGR cycle.

  18. /Air Atmospheres

    NASA Astrophysics Data System (ADS)

    Emami, Samar; Sohn, Hong Yong; Kim, Hang Goo

    2014-08-01

    Molten magnesium oxidizes rapidly when exposed to air causing melt loss and handling difficulties. The use of certain additive gases such as SF6, SO2, and CO2 to form a protective MgO layer over a magnesium melt has been proposed. The oxidation behavior of molten magnesium in air containing various concentrations of SF6 was investigated. Measurements of the kinetics of the oxide layer growth at various SF6 concentrations in air and temperatures were made. Experiments were performed using a thermogravimetric analysis unit in the temperature range of 943 K to 1043 K (670 °C to 770 °C). Results showed that a thin, coherent, and protective MgF2 layer was formed under SF6/Air mixtures, with a thickness ranging from 300 nm to 3 μm depending on SF6 concentration, temperature, and exposure time. Rate parameters were calculated and a model for the process was developed. The morphology and composition of the surface films were studied using scanning electron microscope and energy-dispersive spectroscope.

  19. Air quality at Santiago, Chile: a box modeling approach—I. Carbon monoxide, nitrogen oxides and sulfur dioxide

    NASA Astrophysics Data System (ADS)

    Jorquera, Héctor

    Ambient monitored data at Santiago, Chile, are analyzed using box models with the goal of assessing contributions of different economic activities to air pollution levels. The period analyzed is 1990-2000, characterized by the introduction of air pollution emissions standards, shift to unleaded gasoline and compressed natural gas, and steady growth of the private and public fleet and the associated fuel consumption growth. The box models explicitly include the seasonal behavior of meteorological variables; the results show that dispersion conditions in fall and winter seasons are 20-30% of the summertime values. This result explains the poor air quality in those seasons and shows that significant emissions reductions are required in order to improve air quality in wintertime. Emissions of CO, NO x and SO 2 are estimated from data on fuel consumption in the city; the estimated parameters are thus fleet-average or industry-average emission factors. In terms of contributions to ambient concentrations, older cars and diesel vehicles are the major contributors to CO and NO x impacts, with more than 60% and 50%, respectively. Ambient concentrations of SO 2 are largely dominated by stationary sources, although long range contributions are not negligible. By contrast, CO and NO x pollution is dominated by local sources within the city boundaries. The box models can be used for forecasting purposes, and they can predict annual average concentrations within 20% of the observed values. The methodology requires data on ambient air quality measurements and fuel consumption statistics, and produces quantitative results, which can be combined with economic models to analyze environmental regulation and public policies.

  20. Formation of gas-phase carbonyls from heterogeneous oxidation of polyunsaturated fatty acids at the air-water interface and of the sea surface microlayer

    NASA Astrophysics Data System (ADS)

    Zhou, S.; Gonzalez, L.; Leithead, A.; Finewax, Z.; Thalman, R.; Vlasenko, A.; Vagle, S.; Miller, L. A.; Li, S.-M.; Bureekul, S.; Furutani, H.; Uematsu, M.; Volkamer, R.; Abbatt, J.

    2014-02-01

    Motivated by the potential for reactive heterogeneous chemistry occurring at the ocean surface, gas-phase products were observed when a reactive sea surface microlayer (SML) component, i.e. the polyunsaturated fatty acids (PUFA) linoleic acid (LA), was exposed to gas-phase ozone at the air-seawater interface. Similar oxidation experiments were conducted with SML samples collected from two different oceanic locations, in the eastern equatorial Pacific Ocean and from the west coast of Canada. Online proton-transfer-reaction mass spectrometry (PTR-MS) University of Colorado light-emitting diode cavity-enhanced differential optical absorption spectroscopy (LED-CE-DOAS) were used to detect oxygenated gas-phase products from the ozonolysis reactions. The LA studies indicate that oxidation of a PUFA monolayer on seawater gives rise to prompt and efficient formation of gas-phase aldehydes. The products are formed via the decomposition of primary ozonides which form upon the initial reaction of ozone with the carbon-carbon double bonds in the PUFA molecules. In addition, two highly reactive dicarbonyls, malondialdehyde (MDA) and glyoxal, were also generated, likely as secondary products. Specific yields relative to reactant loss were 78%, 29%, 4% and < 1% for n-hexanal, 3-nonenal, MDA and glyoxal, respectively, where the yields for MDA and glyoxal are likely lower limits. Heterogeneous oxidation of SML samples confirm for the first time that similar carbonyl products are formed via ozonolysis of environmental samples.

  1. Speciation and fate of trace metals in estuarine sediments under reduced and oxidized conditions, Seaplane Lagoon, Alameda Naval Air Station (USA)

    PubMed Central

    Carroll, Susan; O'Day, Peggy A; Esser, Brad; Randall, Simon

    2002-01-01

    We have identified important chemical reactions that control the fate of metal-contaminated estuarine sediments if they are left undisturbed (in situ) or if they are dredged. We combined information on the molecular bonding of metals in solids from X-ray absorption spectroscopy (XAS) with thermodynamic and kinetic driving forces obtained from dissolved metal concentrations to deduce the dominant reactions under reduced and oxidized conditions. We evaluated the in situ geochemistry of metals (cadmium, chromium, iron, lead, manganese and zinc) as a function of sediment depth (to 100 cm) from a 60 year record of contamination at the Alameda Naval Air Station, California. Results from XAS and thermodynamic modeling of porewaters show that cadmium and most of the zinc form stable sulfide phases, and that lead and chromium are associated with stable carbonate, phosphate, phyllosilicate, or oxide minerals. Therefore, there is minimal risk associated with the release of these trace metals from the deeper sediments contaminated prior to the Clean Water Act (1975) as long as reducing conditions are maintained. Increased concentrations of dissolved metals with depth were indicative of the formation of metal HS- complexes. The sediments also contain zinc, chromium, and manganese associated with detrital iron-rich phyllosilicates and/or oxides. These phases are recalcitrant at near-neutral pH and do not undergo reductive dissolution within the 60 year depositional history of sediments at this site. The fate of these metals during dredging was evaluated by comparing in situ geochemistry with that of sediments oxidized by seawater in laboratory experiments. Cadmium and zinc pose the greatest hazard from dredging because their sulfides were highly reactive in seawater. However, their dissolved concentrations under oxic conditions were limited eventually by sorption to or co-precipitation with an iron (oxy)hydroxide. About 50% of the reacted CdS and 80% of the reacted ZnS were

  2. Mesostructured amorphous manganese oxides: facile synthesis and highly durable elimination of low-concentration NO at room temperature in air.

    PubMed

    Du, Yanyan; Hua, Zile; Huang, Weimin; Wu, Meiying; Wang, Min; Wang, Jin; Cui, Xiangzhi; Zhang, Lingxia; Chen, Hangrong; Shi, Jianlin

    2015-04-01

    At a high space velocity of 120 000 mL g(-1) h(-1) and a relative humidity of 50-90%, 98% removal of 10 ppm NO has been achieved for over 237 h and no sign of deactivation was observed with mesostructured amorphous manganese oxides (AMO), due to the prevention of the catalyst active sites from deactivation. PMID:25728967

  3. Regional Air Quality Model Application of the Aqueous-Phase Photo Reduction of Atmospheric Oxidized Mercury by Dicarboxylic Acids

    EPA Science Inventory

    In most ecosystems, atmospheric deposition is the primary input of mercury. The total wet deposition of mercury in atmospheric chemistry models is sensitive to parameterization of the aqueous-phase reduction of divalent oxidized mercury (Hg2+). However, most atmospheric chemistry...

  4. Highlights from Faraday Discussion 182: Solid Oxide Electrolysis: Fuels and Feedstocks from Water and Air, York, UK, July 2015.

    PubMed

    Stefan, Elena; Norby, Truls

    2016-01-31

    The rising importance of converting high peak electricity from renewables to fuels has urged field specialists to organize this Faraday Discussion on Solid Oxide Electrolysis. The topic is of essential interest in order to achieve a greater utilization of renewable energy and storage at higher densities. PMID:26758816

  5. CONTROL OF AIR POLLUTION EMISSIONS FROM MOLYBDENUM ROASTING. VOLUME 3. PILOT SCALE TEST RESULTS FOR MAGNESIUM OXIDE SCRUBBING

    EPA Science Inventory

    A research project was conducted to determine the feasibility of applying the magnesium oxide (MgO) scrubbing system to smelter off-gas streams containing approximately one percent SO2. Pilot scale (4000 cu Nm/hr) tests of the MgO system using a packed tower absorber with no rege...

  6. Comparison of effects of ProSeal LMA™ laryngeal mask airway cuff inflation with air, oxygen, air:oxygen mixture and oxygen:nitrous oxide mixture in adults: A randomised, double-blind study

    PubMed Central

    Sharma, Mona; Sinha, Renu; Trikha, Anjan; Ramachandran, Rashmi; Chandralekha, C

    2016-01-01

    Background and Aims: Laryngeal mask airway (LMA) cuff pressure increases when the air is used for the cuff inflation during oxygen: nitrous oxide (O2:N2O) anaesthesia, which may lead to various problems. We compared the effects of different gases for ProSeal LMA™ (PLMA) cuff inflation in adult patients for various parameters. Methods: A total of 120 patients were randomly allocated to four groups, according to composition of gases used to inflate the PLMA cuff to achieve 40 cmH2 O cuff pressure, air (Group A), 50% O2 :air (Group OA), 50% O2:N2O (Group ON) and 100% O2 (Group O). Cuff pressure, cuff volume and ventilator parameters were monitored intraoperatively. Pharyngolaryngeal parameters were assessed at 1, 2 and 24 h postoperatively. Statistical analysis was performed using ANOVA, Fisher's exact test and step-wise logistic regression. Results: Cuff pressure significantly increased at 10, 15 and 30 min in Group A, OA and O from initial pressure. Cuff pressure decreased at 5 min in Group ON (36.6 ± 3.5 cmH2 O) (P = 0.42). PLMA cuff volume increased in Group A, OA, O, but decreased in Group ON (6.16 ± 2.8 ml [P < 0.001], 4.7 ± 3.8 ml [P < 0.001], 1.4 ± 3.19 ml [P = 0.023] and − 1.7 ± 4.9 ml [P = 0.064], respectively), from basal levels. Ventilatory parameters were comparable in all four groups. There was no significant association between sore throat and cuff pressure, with odds ratio 1.002. Conclusion: Cuff inflation with 50% O2:N2O mixture provided more stable cuff pressure in comparison to air, O2 :air, 100% O2 during O2:N2O anaesthesia. Ventilatory parameters did not change with variation in PLMA cuff pressure. Post-operative sore throat had no correlation with cuff pressure. PMID:27601739

  7. Real-time measurements of secondary organic aerosol formation and aging from ambient air in an oxidation flow reactor in the Los Angeles area

    DOE PAGESBeta

    Ortega, Amber M.; Hayes, Patrick L.; Peng, Zhe; Palm, Brett B.; Hu, Weiwei; Day, Douglas A.; Li, Rui; Cubison, Michael J.; Brune, William H.; Graus, Martin; et al

    2016-06-15

    Field studies in polluted areas over the last decade have observed large formation of secondary organic aerosol (SOA) that is often poorly captured by models. The study of SOA formation using ambient data is often confounded by the effects of advection, vertical mixing, emissions, and variable degrees of photochemical aging. An oxidation flow reactor (OFR) was deployed to study SOA formation in real-time during the California Research at the Nexus of Air Quality and Climate Change (CalNex) campaign in Pasadena, CA, in 2010. A high-resolution aerosol mass spectrometer (AMS) and a scanning mobility particle sizer (SMPS) alternated sampling ambient andmore » reactor-aged air. The reactor produced OH concentrations up to 4 orders of magnitude higher than in ambient air. OH radical concentration was continuously stepped, achieving equivalent atmospheric aging of 0.8 days–6.4 weeks in 3 min of processing every 2 h. Enhancement of organic aerosol (OA) from aging showed a maximum net SOA production between 0.8–6 days of aging with net OA mass loss beyond 2 weeks. Reactor SOA mass peaked at night, in the absence of ambient photochemistry and correlated with trimethylbenzene concentrations. Reactor SOA formation was inversely correlated with ambient SOA and Ox, which along with the short-lived volatile organic compound correlation, indicates the importance of very reactive (τOH ~ 0.3 day) SOA precursors (most likely semivolatile and intermediate volatility species, S/IVOCs) in the Greater Los Angeles Area. Evolution of the elemental composition in the reactor was similar to trends observed in the atmosphere (O : C vs. H : C slope ~ –0.65). Oxidation state of carbon (OSc) in reactor SOA increased steeply with age and remained elevated (OSC ~ 2) at the highest photochemical ages probed. The ratio of OA in the reactor output to excess CO (ΔCO, ambient CO above regional background) vs. photochemical age is similar to previous studies at low to moderate ages and

  8. Real-time measurements of secondary organic aerosol formation and aging from ambient air in an oxidation flow reactor in the Los Angeles area

    NASA Astrophysics Data System (ADS)

    Ortega, Amber M.; Hayes, Patrick L.; Peng, Zhe; Palm, Brett B.; Hu, Weiwei; Day, Douglas A.; Li, Rui; Cubison, Michael J.; Brune, William H.; Graus, Martin; Warneke, Carsten; Gilman, Jessica B.; Kuster, William C.; de Gouw, Joost; Gutiérrez-Montes, Cándido; Jimenez, Jose L.

    2016-06-01

    Field studies in polluted areas over the last decade have observed large formation of secondary organic aerosol (SOA) that is often poorly captured by models. The study of SOA formation using ambient data is often confounded by the effects of advection, vertical mixing, emissions, and variable degrees of photochemical aging. An oxidation flow reactor (OFR) was deployed to study SOA formation in real-time during the California Research at the Nexus of Air Quality and Climate Change (CalNex) campaign in Pasadena, CA, in 2010. A high-resolution aerosol mass spectrometer (AMS) and a scanning mobility particle sizer (SMPS) alternated sampling ambient and reactor-aged air. The reactor produced OH concentrations up to 4 orders of magnitude higher than in ambient air. OH radical concentration was continuously stepped, achieving equivalent atmospheric aging of 0.8 days-6.4 weeks in 3 min of processing every 2 h. Enhancement of organic aerosol (OA) from aging showed a maximum net SOA production between 0.8-6 days of aging with net OA mass loss beyond 2 weeks. Reactor SOA mass peaked at night, in the absence of ambient photochemistry and correlated with trimethylbenzene concentrations. Reactor SOA formation was inversely correlated with ambient SOA and Ox, which along with the short-lived volatile organic compound correlation, indicates the importance of very reactive (τOH ˜ 0.3 day) SOA precursors (most likely semivolatile and intermediate volatility species, S/IVOCs) in the Greater Los Angeles Area. Evolution of the elemental composition in the reactor was similar to trends observed in the atmosphere (O : C vs. H : C slope ˜ -0.65). Oxidation state of carbon (OSc) in reactor SOA increased steeply with age and remained elevated (OSC ˜ 2) at the highest photochemical ages probed. The ratio of OA in the reactor output to excess CO (ΔCO, ambient CO above regional background) vs. photochemical age is similar to previous studies at low to moderate ages and also extends to

  9. Nitric oxide formation in a lean, premixed-prevaporized jet A/air flame tube: An experimental and analytical study

    NASA Technical Reports Server (NTRS)

    Lee, Chi-Ming; Bianco, Jean; Deur, John M.; Ghorashi, Bahman

    1992-01-01

    An experimental and analytical study was performed on a lean, premixed-prevaporized Jet A/air flame tube. The NO(x) emissions were measured in a flame tube apparatus at inlet temperatures ranging from 755 to 866 K (900 to 1100 F), pressures from 10 to 15 atm, and equivalence ratios from 0.37 to 0.62. The data were then used in regressing an equation to predict the NO(x) production levels in combustors of similar design. Through an evaluation of parameters it was found that NO(x) is dependent on adiabatic flame temperature and combustion residence time, yet independent of pressure and inlet air temperature for the range of conditions studied. This equation was then applied to experimental data that were obtained from the literature, and a good correlation was achieved.

  10. Hydrogen oxidation mechanism with applications to (1) the chaperon efficiency of carbon dioxide and (2) vitiated air testing

    NASA Technical Reports Server (NTRS)

    Brabbs, Theodore A.; Lezberg, Erwin A.; Bittker, David A.; Robertson, Thomas F.

    1987-01-01

    Ignition delay times for the hydrogen/oxygen/carbon dioxide/argon system were obtained behind reflected shock waves. A detailed kinetic mechanism modeled the experimental hydrogen/oxygen data, Skinner and Ringrose's high-pressure data, and Slack and Grillo's hydrogen/air data. A carbon dioxide chaperon efficiency of 7.0 +/- 0.2 was determined. The reaction pathway H2O yields H2O2 yields OH yields H was required to model the high-pressure data. It is suggested that some of the lowest temperature data points (1.0 and 0.5 atm) for Slack and Grillo's hydrogen/air experiments are in error. It was found that the technique of simplifying a detailed kinetic mechanism for a limited range of experimental data may render the model useless for other test conditions.

  11. Air pollution upregulates endothelial cell procoagulant activity via ultrafine particle-induced oxidant signaling and tissue factor expression.

    PubMed

    Snow, S J; Cheng, W; Wolberg, A S; Carraway, M S

    2014-07-01

    Air pollution exposure is associated with cardiovascular events triggered by clot formation. Endothelial activation and initiation of coagulation are pathophysiological mechanisms that could link inhaled air pollutants to vascular events. Here we investigated the underlying mechanisms of increased endothelial cell procoagulant activity following exposure to soluble components of ultrafine particles (soluble UF). Human coronary artery endothelial cells (HCAEC) were exposed to soluble UF and assessed for their ability to trigger procoagulant activity in platelet-free plasma. Exposed HCAEC triggered earlier thrombin generation and faster fibrin clot formation, which was abolished by an anti-tissue factor (TF) antibody, indicating TF-dependent effects. Soluble UF exposure increased TF mRNA expression without compensatory increases in key anticoagulant proteins. To identify early events that regulate TF expression, we measured endothelial H2O2 production following soluble UF exposure and identified the enzymatic source. Soluble UF exposure increased endothelial H2O2 production, and antioxidants attenuated UF-induced upregulation of TF, linking the procoagulant responses to reactive oxygen species (ROS) formation. Chemical inhibitors and RNA silencing showed that NOX-4, an important endothelial source of H2O2, was involved in UF-induced upregulation of TF mRNA. These data indicate that soluble UF exposure induces endothelial cell procoagulant activity, which involves de novo TF synthesis, ROS production, and the NOX-4 enzyme. These findings provide mechanistic insight into the adverse cardiovascular effects associated with air pollution exposure. PMID:24752501

  12. Smoking and Cerebral Oxidative Stress and Air Pollution: A Dreadful Equation with Particulate Matter Involved and One More Powerful Reason Not to Smoke Anything!

    PubMed

    Calderón-Garcidueñas, Lilian

    2016-07-22

    Smoking has serious health effects. Cigarettes, including tobacco, marijuana, and electronic nicotine delivery systems are very effective ways to inhale harmful amounts of fine and ultrafine particulate matter. Does size matter? Yes, indeed! The smaller the particle you inhale, the higher the ability to produce reactive oxygen species and to readily access the brain. In this issue of the Journal of Alzheimer's Disease, Durazzo provides evidence of an association between active cigarette tobacco smoking in cognitively-normal elders and increased cerebral oxidative stress, while in actively smoking Alzheimer's disease (AD) patients, the association was also seen with smaller left and total hippocampal volumes. This paper has highly relevant results of interest across the US and the world because millions of people are active smokers and they have other genetic and environmental risk factors that could play a key role in the development/worsening of brain oxidative stress and neurodegeneration. Smoking basically anything producing aerosols with particulate matter in the fine and ultrafine size range is detrimental to your brain. Marijuana and e-cigarette use has grown steadily among adolescents and young adults. Smoking-related cerebral oxidative stress is a potential mechanism promoting AD pathology and increased risk for AD. Current knowledge also relates fine and ultrafine particles exposures influencing neurodevelopmental processes in utero. The results from Durazzo et al. should be put in a broader context, a context that includes evaluating the oxidative stress of nano-aerosols associated with cigarette emissions and their synergistic effects with air pollution exposures. AD is expected to increase in the US threefold by the year 2050, and some of these future AD patients are smoking and vaping right now. Understanding the impact of everyday exposures to long-term harmful consequences for brain health is imperative. PMID:27447427

  13. Air Pollution, Causes and Cures.

    ERIC Educational Resources Information Center

    Manufacturing Chemists Association, Washington, DC.

    This commentary on sources of air pollution and air purification treatments is accompanied by graphic illustrations. Sources of carbon monoxide, sulfur oxides, nitrogen oxides, and hydrocarbons found in the air are discussed. Methods of removing these pollutants at their source are presented with cut-away diagrams of the facilities and technical…

  14. A high-fidelity multiphysics model for the new solid oxide iron-air redox battery. part I: Bridging mass transport and charge transfer with redox cycle kinetics

    NASA Astrophysics Data System (ADS)

    Jin, Xinfang; Zhao, Xuan; Huang, Kevin

    2015-04-01

    A high-fidelity two-dimensional axial symmetrical multi-physics model is described in this paper as an effort to simulate the cycle performance of a recently discovered solid oxide metal-air redox battery (SOMARB). The model collectively considers mass transport, charge transfer and chemical redox cycle kinetics occurring across the components of the battery, and is validated by experimental data obtained from independent research. In particular, the redox kinetics at the energy storage unit is well represented by Johnson-Mehl-Avrami-Kolmogorov (JMAK) and Shrinking Core models. The results explicitly show that the reduction of Fe3O4 during the charging cycle limits the overall performance. Distributions of electrode potential, overpotential, Nernst potential, and H2/H2O-concentration across various components of the battery are also systematically investigated.

  15. Field emission in air and space-charge-limited currents from iridium-iridium oxide tips with gaps below 100 nm

    NASA Astrophysics Data System (ADS)

    Brimley, Scott; Miller, Mark S.; Hagmann, Mark J.

    2011-05-01

    Field emission diodes made with Ir/IrO2 tips separated by gaps below 100 nm and operating in air gave currents of up to 1 μA just above 10 V and largely survived potentials up to 200 V. The current-voltage characteristics included signatures of Fowler-Nordheim emission and both coherent and incoherent space-charge limited emission, where both behaviors implied molecular-scale effective emission areas. The significant, nanoampere currents that flowed at biases below the expected bulk work functions corroborate the 0.1 eV work functions from Fowler-Nordheim analysis, and are attributed to molecular scale oxide structures and adsorbates shifting the surface Fermi level. Electron transit time analysis indicates that on average only one electron crossed the gap at a time, implying that the space-charge effects are due to self-interactions.

  16. A high-fidelity multiphysics model for the new solid oxide iron-air redox battery part I: Bridging mass transport and charge transfer with redox cycle kinetics

    SciTech Connect

    Jin, XF; Zhao, X; Huang, K

    2015-04-15

    A high-fidelity two-dimensional axial symmetrical multi-physics model is described in this paper as an effort to simulate the cycle performance of a recently discovered solid oxide metal-air redox battery (SOMARB). The model collectively considers mass transport, charge transfer and chemical redox cycle kinetics occurring across the components of the battery, and is validated by experimental data obtained from independent research. In particular, the redox kinetics at the energy storage unit is well represented by Johnson-Mehl-Avrami-Kolmogorov (JIVIAK) and Shrinking Core models. The results explicitly show that the reduction of Fe3O4 during the charging cycle limits the overall performance. Distributions of electrode potential, overpotential, Nernst potential, and H-2/H2O-concentration across various components of the battery are also systematically investigated. (C) 2015 Elsevier B.V. All rights reserved.

  17. Evaluation of chromium oxide and molybdenum disulfide coatings in self-acting stops of an air-lubricated Rayleigh step thrust bearing

    NASA Technical Reports Server (NTRS)

    Nemeth, Z. N.

    1974-01-01

    Two coatings for a Rayleigh step thrust bearing were tested when coasting down and stopping under self-acting operation in air. The thrust bearing had an outside diameter of 8.9 cm (3.5 in.), an inside diameter of 5.4 cm (2.1 in.), and nine sectors. The load was 73 N (16.4 lbf). The load pressure was 19.1 kN/per square meter (2.77 lbf/per square inch) on the total thrust bearing area. The chromium oxide coating was good to 150 stops without bearing deterioration, and the molybdenum disulfide coating was good for only four stops before bearing deterioration. The molybdenum disulfide coated bearing failed after nine stops.

  18. Bioleaching of heavy metals from contaminated sediment by indigenous sulfur-oxidizing bacteria in an air-lift bioreactor: effects of sulfur concentration.

    PubMed

    Chen, Shen-Yi; Lin, Jih-Gaw

    2004-01-01

    The effects of sulfur concentration on the bioleaching of heavy metals from the sediment by indigenous sulfur-oxidizing bacteria were investigated in an air-lift reactor. Increasing the sulfur concentration from 0.5 to 5 g/l enhanced the rates of pH reduction, sulfate production and metal solubilization. A Michaelis-Menten type equation was used to explain the relationships between sulfur concentration, sulfate production and metal solubilization in the bioleaching process. After 8 days of bioleaching, 97-99% of Cu, 96-98% of Zn, 62-68% of Mn, 73-87% of Ni and 31-50% of Pb were solubilized from the sediment, respectively. The efficiency of metal solubilization was found to be related to the speciation of metal in the sediment. From economical consideration, the recommended sulfur dosage for the bioleaching of metals from the sediment is 3g/l. PMID:15276736

  19. Health effects from the inhalation of oxidant air pollutants as related to the immune system. Final report. Research report

    SciTech Connect

    Osebold, J.W.; Zee, Y.C.

    1985-07-01

    The investigations dealt with links between ozone inhalation and lung diseases. Mice exposed to ozone both continuously and intermittently in four-day cycles showed allergic sensitization to the test antigen (ovalbumin) when compaired to mice maintained in ambeint air. An adjuvant (inactivated Bordetella pertussis cells) administered to mice augmented the immunological response to the test antigen with periodic exposure to ozone. Guinea pigs were tested for allergic sensitization from ozone exposure similar to human asthma, but this trial was not definitive. Ozone inhalation reduced the severity of pneumonia in mice from influenza virus infection, even when ozone and virus exposures were timed to produce maximal edema in the lung.

  20. Comparing universal kriging and land-use regression for predicting concentrations of gaseous oxides of nitrogen (NO x) for the Multi-Ethnic Study of Atherosclerosis and Air Pollution (MESA Air)

    NASA Astrophysics Data System (ADS)

    Mercer, Laina D.; Szpiro, Adam A.; Sheppard, Lianne; Lindström, Johan; Adar, Sara D.; Allen, Ryan W.; Avol, Edward L.; Oron, Assaf P.; Larson, Timothy; Liu, L.-J. Sally; Kaufman, Joel D.

    2011-08-01

    BackgroundEpidemiological studies that assess the health effects of long-term exposure to ambient air pollution are used to inform public policy. These studies rely on exposure models that use data collected from pollution monitoring sites to predict exposures at subject locations. Land-use regression (LUR) and universal kriging (UK) have been suggested as potential prediction methods. We evaluate these approaches on a dataset including measurements from three seasons in Los Angeles, CA. MethodsThe measurements of gaseous oxides of nitrogen (NO x) used in this study are from a "snapshot" sampling campaign that is part of the Multi-Ethnic Study of Atherosclerosis and Air Pollution (MESA Air). The measurements in Los Angeles were collected during three two-week periods in the summer, autumn, and winter, each with about 150 sites. The design included clusters of monitors on either side of busy roads to capture near-field gradients of traffic-related pollution. LUR and UK prediction models were created using geographic information system (GIS)-based covariates. Selection of covariates was based on 10-fold cross-validated (CV) R2 and root mean square error (RMSE). Since UK requires specialized software, a computationally simpler two-step procedure was also employed to approximate fitting the UK model using readily available regression and GIS software. ResultsUK models consistently performed as well as or better than the analogous LUR models. The best CV R2 values for season-specific UK models predicting log(NO x) were 0.75, 0.72, and 0.74 (CV RMSE 0.20, 0.17, and 0.15) for summer, autumn, and winter, respectively. The best CV R2 values for season-specific LUR models predicting log(NO x) were 0.74, 0.60, and 0.67 (CV RMSE 0.20, 0.20, and 0.17). The two-stage approximation to UK also performed better than LUR and nearly as well as the full UK model with CV R2 values 0.75, 0.70, and 0.70 (CV RMSE 0.20, 0.17, and 0.17) for summer, autumn, and winter, respectively

  1. Inducible Nitric Oxide Synthase Promoter Haplotypes and Residential Traffic-Related Air Pollution Jointly Influence Exhaled Nitric Oxide Level in Children

    PubMed Central

    Salam, Muhammad T.; Lin, Pi-Chu; Eckel, Sandrah P.; Gauderman, W. James; Gilliland, Frank D.

    2015-01-01

    Background Exhaled nitric oxide (FeNO), a biomarker of airway inflammation, predicts asthma risk in children. We previously found that the promoter haplotypes in inducible nitric oxide synthase (NOS2) and exposure to residential traffic independently influence FeNO level. Because NOS2 is inducible by environmental exposures such as traffic-related exposure, we tested the hypothesis that common NOS2 promoter haplotypes modulate the relationship between residential traffic-related exposure and FeNO level in children. Methods In a cross-sectional population-based study, subjects (N = 2,457; 7–11 year-old) were Hispanic and non-Hispanic white children who participated in the Southern California Children’s Health Study and had FeNO measurements. For residential traffic, lengths of local roads within circular buffers (50m, 100m and 200m radii around homes) around the subjects’ homes were estimated using geographic information system (GIS) methods. We interrogated the two most common NOS2 promoter haplotypes that were found to affect FeNO level. Results The relationship between local road lengths within 100m and 200m circular buffers and FeNO level varied significantly by one of the NOS2 promoter haplotypes (P-values for interaction between road length and NOS2 promoter haplotype = 0.02 and 0.03, respectively). In children who had ≤250m of local road lengths within 100m buffer around their homes, those with two copies of the haplotype had significantly lower FeNO (adjusted geometric mean = 11.74ppb; 95% confidence intervals (CI): 9.99 to 13.80) than those with no copies (adjusted geometric mean = 15.28ppb; 95% CI: 14.04 to 16.63) with statistically significant trend of lower FeNO level with increasing number of haplotype copy (P-value for trend = 0.002). In contrast, among children who had >250m of local road lengths within 100m buffer, FeNO level did not significantly differ by the haplotype copy-number (P-value for trend = 0.34). Similar interactive effects of

  2. Modeling the oxidative capacity of the atmosphere of the south coast air basin of California. 2. HOx radical production.

    PubMed

    Griffin, Robert J

    2004-02-01

    The production of HOx radicals in the South Coast Air Basin of California is investigated during the smog episode of September 9, 1993 using the California Institute of Technology (CIT) air-quality model. Sources of HOx(hydroxyl, hydroperoxy, and organic peroxy radicals) incorporated into the associated gas-phase chemical mechanism include the combination of excited-state singlet oxygen (formed from ozone (O3) photolysis (hv)) with water, the photolysis of nitrous acid, hydrogen peroxide (H2O2), and carbonyl compounds (formaldehyde (HCHO) or higher aldehydes and ketones), the consumption of aldehydes and alkenes (ALK) by the nitrate radical, and the consumption of alkenes by O3 and the oxygen atom (O). At a given time or location for surface cells and vertical averages, each route of HOx formation may be the greatest contributor to overall formation except HCHO-hv, H2O2-hv, and ALK-O, the latter two of which are insignificant pathways in general. The contribution of the ALK-O3 pathway is dependent on the stoichiometric yield of OH, but this pathway, at least for the studied smog episode, may not be as generally significant as previous research suggests. Future emissions scenarios yield lower total HOx production rates and a shift in the relative importance of individual pathways. PMID:14968860

  3. Simplified Two-Time Step Method for Calculating Combustion Rates and Nitrogen Oxide Emissions for Hydrogen/Air and Hydorgen/Oxygen

    NASA Technical Reports Server (NTRS)

    Molnar, Melissa; Marek, C. John

    2005-01-01

    A simplified single rate expression for hydrogen combustion and nitrogen oxide production was developed. Detailed kinetics are predicted for the chemical kinetic times using the complete chemical mechanism over the entire operating space. These times are then correlated to the reactor conditions using an exponential fit. Simple first order reaction expressions are then used to find the conversion in the reactor. The method uses a two-time step kinetic scheme. The first time averaged step is used at the initial times with smaller water concentrations. This gives the average chemical kinetic time as a function of initial overall fuel air ratio, temperature, and pressure. The second instantaneous step is used at higher water concentrations (> 1 x 10(exp -20) moles/cc) in the mixture which gives the chemical kinetic time as a function of the instantaneous fuel and water mole concentrations, pressure and temperature (T4). The simple correlations are then compared to the turbulent mixing times to determine the limiting properties of the reaction. The NASA Glenn GLSENS kinetics code calculates the reaction rates and rate constants for each species in a kinetic scheme for finite kinetic rates. These reaction rates are used to calculate the necessary chemical kinetic times. This time is regressed over the complete initial conditions using the Excel regression routine. Chemical kinetic time equations for H2 and NOx are obtained for H2/air fuel and for the H2/O2. A similar correlation is also developed using data from NASA s Chemical Equilibrium Applications (CEA) code to determine the equilibrium temperature (T4) as a function of overall fuel/air ratio, pressure and initial temperature (T3). High values of the regression coefficient R2 are obtained.

  4. Summary of Simplified Two Time Step Method for Calculating Combustion Rates and Nitrogen Oxide Emissions for Hydrogen/Air and Hydrogen/Oxygen

    NASA Technical Reports Server (NTRS)

    Marek, C. John; Molnar, Melissa

    2005-01-01

    A simplified single rate expression for hydrogen combustion and nitrogen oxide production was developed. Detailed kinetics are predicted for the chemical kinetic times using the complete chemical mechanism over the entire operating space. These times are then correlated to the reactor conditions using an exponential fit. Simple first order reaction expressions are then used to find the conversion in the reactor. The method uses a two time step kinetic scheme. The first time averaged step is used at the initial times with smaller water concentrations. This gives the average chemical kinetic time as a function of initial overall fuel air ratio, temperature, and pressure. The second instantaneous step is used at higher water concentrations (greater than l x 10(exp -20)) moles per cc) in the mixture which gives the chemical kinetic time as a function of the instantaneous fuel and water mole concentrations, pressure and temperature (T(sub 4)). The simple correlations are then compared to the turbulent mixing times to determine the limiting properties of the reaction. The NASA Glenn GLSENS kinetics code calculates the reaction rates and rate constants for each species in a kinetic scheme for finite kinetic rates. These reaction rates are used to calculate the necessary chemical kinetic times. This time is regressed over the complete initial conditions using the Excel regression routine. Chemical kinetic time equations for H2 and NOx are obtained for H2/Air fuel and for H2/O2. A similar correlation is also developed using data from NASA's Chemical Equilibrium Applications (CEA) code to determine the equilibrium temperature (T(sub 4)) as a function of overall fuel/air ratio, pressure and initial temperature (T(sub 3)). High values of the regression coefficient R squared are obtained.

  5. Life cycle inventory analysis of regenerative thermal oxidation of air emissions from oriented strand board facilities in Minnesota - a perspective of global climate change

    SciTech Connect

    Nicholson, W.J.

    1997-12-31

    Life cycle inventory analysis has been applied to the prospective operation of regenerative thermal oxidation (RTO) technology at oriented strand board plants at Bemidji (Line 1) and Cook, Minnesota. The net system destruction of VOC`s and carbon monoxide, and at Cook a small quantity of particulate, has a very high environmental price in terms of energy and water use, global warming potential, sulfur and nitrogen oxide emissions, solids discharged to water, and solid waste deposited in landfills. The benefit of VOC destruction is identified as minor in terms of ground level ozone at best and possibly slightly detrimental. Recognition of environmental tradeoffs associated with proposed system changes is critical to sound decision-making. There are more conventional ways to address carbon monoxide emissions than combustion in RTO`s. In an environment in which global warming is a concern, fuel supplemental combustion for environmental control does not appear warranted. Consideration of non-combustion approaches to address air emission issues at the two operations is recommended. 1 ref., 5 tabs.

  6. Synthesis and characterization of poly(divinylbenzene)-coated magnetic iron oxide nanoparticles as precursor for the formation of air-stable carbon-coated iron crystalline nanoparticles.

    PubMed

    Boguslavsky, Yonit; Margel, Shlomo

    2008-01-01

    Maghemite (gamma-Fe2O3) nanoparticles of 15 +/- 3 nm diameter were prepared by nucleation of gelatin/iron oxide followed by growth of gamma-Fe2O3 films onto these nuclei. The gamma-Fe2O3 nanoparticles were coated with polydivinylbenzene (PDVB) by emulsion polymerization of divinylbenzene (DVB) in an aqueous continuous phase containing the gamma-Fe2O3 nanoparticles. The PDVB-coated gamma-Fe2O3 nanoparticles, dispersed in water, were separated from homo-PDVB nanoparticles using the high gradient magnetic field (HGMF) technique. The influence of DVB concentration on the amount of PDVB coating, on the size and size distribution of the coated gamma-Fe2O3 nanoparticles and on their magnetic properties, has been investigated. Air-stable carbon-coated iron (alpha-Fe/C) crystalline nanoparticles of 41 +/- 12 nm diameter have been prepared by annealing the PDVB-coated gamma-Fe2O3 nanoparticles at 1050 degrees C in an inert atmosphere. These nanoparticles exhibit high saturation magnetization value (83 emu g(-1)) and excellent resistance to oxidation. Characterization of the PDVB-coated gamma-Fe2O3 and of the alpha-Fe/C nanoparticles has been accomplished by TEM, HRTEM, DLS, FTIR, XRD, thermal analysis, zeta-potential, and magnetic measurements. PMID:17927999

  7. The impact of the congestion charging scheme on air quality in London. Part 2. Analysis of the oxidative potential of particulate matter.

    PubMed

    Kelly, Frank; Anderson, H Ross; Armstrong, Ben; Atkinson, Richard; Barratt, Ben; Beevers, Sean; Derwent, Dick; Green, David; Mudway, Ian; Wilkinson, Paul

    2011-04-01

    There is growing scientific consensus that the ability of inhaled particulate matter (PM*) to elicit oxidative stress both at the air-lung interface and systemically might underpin many of the acute and chronic respiratory and cardiovascular responses observed in exposed populations. In the current study (which is part two of a two-part HEI study of a congestion charging scheme [CCS] introduced in London, United Kingdom, in 2003), we tested the hypothesis that the reduction in vehicle numbers and changes in traffic composition resulting from the introduction of the CCS would result in decreased concentrations of traffic-specific emissions, both from vehicle exhaust and other sources (brake wear and tire wear), and an associated reduction in the oxidative potential of PM with an aerodynamic diameter < or = 10 microm (PM10). To test this hypothesis, we obtained, extracted, and analyzed tapered element oscillating microbalance (TEOM) PM10 filters from six monitoring sites within, bordering, or outside the area of the congestion charging zone (CCZ) for the 3 years before and after the introduction of the scheme. In addition, from January 2005, TEOM PM10 filters were obtained from an additional 10 sites outside the zone in order to perform the first-ever assessment of within-city spatial variability in the oxidative potential of PM10. Although London's PM10 was found to have remarkably high oxidative potential, it varied markedly between the studied sites, with evidence of increased potential at roadside locations compared with urban background locations. This difference appeared to reflect increased concentrations of copper (Cu), barium (Ba), and bioavailable iron (Fe) in PM10 collected at the roadside sites. PM10's oxidative potential after the introduction of the CCS did not change at the one urban background site within the zone. Yet compositional changes in PM10 were noted at the same site, including significant decreases in Cu and zinc (Zn) content, probably

  8. Effect of Silicon on Hot Shortness in Fe-Cu-Ni-Sn-Si Alloys During Isothermal Oxidation in Air

    NASA Astrophysics Data System (ADS)

    Sampson, Erica; Sridhar, Seetharaman

    2013-10-01

    Residual Cu in scrap-based EAF steel leads to a surface-cracking phenomenon known as surface hot shortness. Si is known to provide a potential reduction in hot shortness; however, the mechanisms involved are not fully understood for low Si quantities. The current study aims to determine a window of Si contents with a given Ni content needed to counteract the negative effects of Sn and Cu to reduce hot shortness and to determine the mechanism. Thermogravimetric analysis (TG), SEM-EDS, XRD, and TEM were used to study the hot shortness behavior of Fe containing 0.2 pct Cu, 0.05 pct Ni, 0.01 pct Sn and with varying Si-content (0.02 pct, 0.1 pct, 0.15 pct, and 0.2 pct Si). It was found that the fayalite formation resulting in a reduction of oxidation and consequently liquid Cu formation occurred for all Si contents examined. The range of Si contents between 0.1 and 0.2 wt pct Si exhibited a mechanism that was a combination of fayalite formation impeding oxidation as well as occlusion of the Cu-rich liquid. This range was acceptable to alleviate hot shortness.

  9. Formation of gas-phase carbonyls from heterogeneous oxidation of polyunsaturated fatty acids at the air-water interface and of the sea surface microlayer

    NASA Astrophysics Data System (ADS)

    Zhou, S.; Gonzalez, L.; Leithead, A.; Finewax, Z.; Thalman, R.; Vlasenko, A.; Vagle, S.; Miller, L.; Li, S.-M.; Bureekul, S.; Furutani, H.; Uematsu, M.; Volkamer, R.; Abbatt, J.

    2013-07-01

    Motivated by the potential for reactive heterogeneous chemistry occurring at the ocean surface, gas-phase products were observed when a reactive sea surface microlayer (SML) component, i.e. the polyunsaturated fatty acid (PUFA) linoleic acid (LA), was exposed to gas-phase ozone at the air-seawater interface. Similar oxidation experiments were conducted with SML samples collected from two different oceanic locations, in the eastern equatorial Pacific Ocean and from the west coast of Canada. Online proton-transfer-reaction mass spectrometry (PTR-MS) and light-emitting diode cavity enhanced differential optical absorption spectroscopy (LED-CE-DOAS) were used to detect oxygenated gas-phase products from the ozonolysis reactions. The LA studies indicate that oxidation of a PUFA monolayer on seawater gives rise to prompt and efficient formation of gas phase aldehydes. The products are formed via the decomposition of primary ozonides which form upon the initial reaction of ozone with the carbon-carbon double bonds in the PUFA molecules. In addition, two highly reactive di-carbonyls, malondialdehyde (MDA) and glyoxal, were also generated, likely as secondary products. Specific yields relative to reactant loss were 78%, 29%, 4% and <1% for n-hexanal, 3-nonenal, MDA and glyoxal, respectively, where the yields for MDA and glyoxal are likely lower limits. Heterogeneous oxidation of SML samples confirm for the first time that similar carbonyl products are formed via ozonolysis of environmental samples. The potential impact of such chemistry on the atmosphere of the marine boundary layer is discussed.

  10. Perspective: Maintaining surface-phase purity is key to efficient open air fabricated cuprous oxide solar cells

    SciTech Connect

    Hoye, Robert L. Z. E-mail: jld35@cam.ac.uk; Ievskaya, Yulia; MacManus-Driscoll, Judith L. E-mail: jld35@cam.ac.uk; Brandt, Riley E.; Buonassisi, Tonio; Heffernan, Shane; Musselman, Kevin P.

    2015-02-01

    Electrochemically deposited Cu{sub 2}O solar cells are receiving growing attention owing to a recent doubling in efficiency. This was enabled by the controlled chemical environment used in depositing doped ZnO layers by atomic layer deposition, which is not well suited to large-scale industrial production. While open air fabrication with atmospheric pressure spatial atomic layer deposition overcomes this limitation, we find that this approach is limited by an inability to remove the detrimental CuO layer that forms on the Cu{sub 2}O surface. Herein, we propose strategies for achieving efficiencies in atmospherically processed cells that are equivalent to the high values achieved in vacuum processed cells.

  11. Inflammatory and Oxidative Stress Responses of an Alveolar Epithelial Cell Line to Airborne Zinc Oxide Nanoparticles at the Air-Liquid Interface: A Comparison with Conventional, Submerged Cell-Culture Conditions

    PubMed Central

    Lenz, Anke-Gabriele; Karg, Erwin; Brendel, Ellen; Hinze-Heyn, Helga; Maier, Konrad L.; Eickelberg, Oliver; Stoeger, Tobias; Schmid, Otmar

    2013-01-01

    The biological effects of inhalable nanoparticles have been widely studied in vitro with pulmonary cells cultured under submerged and air-liquid interface (ALI) conditions. Submerged exposures are experimentally simpler, but ALI exposures are physiologically more realistic and hence potentially biologically more meaningful. In this study, we investigated the cellular response of human alveolar epithelial-like cells (A549) to airborne agglomerates of zinc oxide (ZnO) nanoparticles at the ALI, compared it to the response under submerged culture conditions, and provided a quantitative comparison with the literature data on different types of particles and cells. For ZnO nanoparticle doses of 0.7 and 2.5 μg ZnO/cm2 (or 0.09 and 0.33 cm2 ZnO/cm2), cell viability was not mitigated and no significant effects on the transcript levels of oxidative stress markers (HMOX1, SOD-2 and GCS) were observed. However, the transcript levels of proinflammatory markers (IL-8, IL-6, and GM-CSF) were induced to higher levels under ALI conditions. This is consistent with the literature data and it suggests that in vitro toxicity screening of nanoparticles with ALI cell culture systems may produce less false negative results than screening with submerged cell cultures. However, the database is currently too scarce to draw a definite conclusion on this issue. PMID:23484138

  12. Twenty years of ambient observations of nitrogen oxides and specified hydrocarbons in air masses dominated by traffic emissions in Germany.

    PubMed

    Ehlers, Christian; Klemp, Dieter; Rohrer, Franz; Mihelcic, Djuro; Wegener, Robert; Kiendler-Scharr, Astrid; Wahner, Andreas

    2016-07-18

    The analysis of the individual composition of hydrocarbon (VOC) mixtures enables us to transform observed VOC-concentrations into their respective total VOC-reactivity versus OH radicals (RVOC = Σ(kOH+VOCi × [VOCi])). This is particularly useful because local ozone production essentially depends on this single parameter rather than on the details of the underlying hydrocarbon mixture (Klemp et al., Schriften des Forschungszentrums Jülich, Energy & Environment, 2012, 21). The VOC composition also enables us to pin down the major emission source of hydrocarbons in urban areas to be petrol cars with temporarily reduced catalyst efficiency (the so-called cold-start situation) whereas the source of nitrogen oxides (NOx = NO + NO2) is expected to be nowadays dominated by diesel cars. The observations in the vicinity of main roads in German cities show a decrease in the ratio of OH reactivities of VOC and NO2 (RVOC/RNO2) by a factor of 7.5 over the time period 1994-2014. This is larger than the expected decrease of a factor of 2.9 taking estimated trends of VOC and NOx traffic emissions in Germany (Umweltbundesamt Deutschland, National Trend Tables for the German Atmospheric Emission Reporting, 2015), during this time period. The observed reduction in the RVOC/RNO2 ratio leads to a drastic decrease in local ozone production driven by the reduction in hydrocarbons. The analysis reveals that the overall reduction of ozone production benefits from the low decrease of NOx emissions from road traffic which is a consequence of the eventual absence of catalytic converters for nitrogen oxide removal in diesel cars up to now. PMID:27117015

  13. Supplement to the Second Addendum (1986) to Air Quality Criteria for Particulate Matter and Sulfur Oxides (1982): Assessment of New Findings on Sulfur Dioxide and Acute Exposure Health Effects in Asthmatic Individuals (1994)

    EPA Science Inventory

    The present Supplement to the Second Addendum (1986) to the document Air Quality Criteria for Particulate Matter and Sulfur Oxides (1982) focuses on evaluation of newly available controlled human exposure studies of acute (a\\1h) sulfur dioxide (SO2) exposure effects on pulmonary ...

  14. Characterization and Oxidation Behaviour of Al2O3 Coating Deposited on Ti-Al-Nb Alloy in Air and in 9%O2 + 0.2%HCl + 0.08%SO2 + N2 Atmosphere

    NASA Astrophysics Data System (ADS)

    Małecka, Joanna

    2015-02-01

    The paper presents research results of isothermal oxidation of Ti-46Al-7Nb-0.7Cr-0.1Si-0.1Ni intermetallic alloy with Al2O3 coating. Oxidation was carried out in air and in the atmosphere with the content 9%O2 + 0.2%HCl + 0.08%SO2 + N2 at 750 °C. Mass changes of the specimens were recorded after 50, 100, 300 and 500 hours. The surface morphology of the oxidized samples were studied using Scanning Electron Microscopy (SEM), Wavelength Dispersive Spectroscopy (WDS) and Energy Dispersive Spectroscopy (EDS). The results obtained showed that the corrosion resistance of the examined alloy is better in air. The oxidation in the atmosphere of 9%O2 + 0.2%HCl + 0.08%SO2 + N2 causes the formation of eruptions of Al2O3 and TiO2 mixture, however, in air the forming oxide layer is suppressed by the deposited protective Al2O3 coating.

  15. Oxidation kinetics and microstructure of V-(4-5) Wt.%Cr-(4-5) Wt.%Ti alloys exposed to air at 300-650{degrees}C

    SciTech Connect

    Natesan, K.; Uz, M.

    1996-10-01

    A systematic study was conducted to determine the effects of time and temperature of air exposure on the oxidation behavior and microstructure of V-4Cr-4Ti (44) and V-5Cr-5Ti (55) alloys. All samples were from 1-mm-thick cold-rolled sheets, and each was annealed in vacuum at 1050{degrees}C for 1 h prior to high-temperature exposure. Different samples from each alloy were heated in ambient air at 500{degrees}C for times ranging from 24 to {approx}2000 h, and in a thermogravimetric analysis (TGA) apparatus at 300 to 650{degrees}C. Models describing the oxidation kinetics, the oxide type and its thickness, alloy grain size, and the depth of oxygen diffusion in the substrate alloy were determined for the two alloys and compared. The results showed that the oxide layers that formed on the surfaces of both alloys in air in the temperature range of 300-650{degrees}C are protective, and that the 55 alloy is slightly more oxidation-resistant than the 44 alloy.

  16. Modeling the oxidative capacity of the atmosphere of the south coast air basin of California. 1. Ozone formation metrics.

    PubMed

    Griffin, Robert J; Revelle, Meghan K; Dabdub, Donald

    2004-02-01

    Metrics associated with ozone (O3) formation are investigated using the California Institute of Technology (CIT) three-dimensional air-quality model. Variables investigated include the O3 production rate (P(O3)), O3 production efficiency (OPE), and total reactivity (the sum of the reactivity of carbon monoxide (CO) and all organic gases that react with the hydroxyl radical). Calculations are spatially and temporally resolved; surface-level and vertically averaged results are shown for September 9, 1993 for three Southern California locations: Central Los Angeles, Azusa, and Riverside. Predictions indicate increasing surface-level O3 concentrations with distance downwind, in line with observations. Surface-level and vertically averaged P(O3) values peak during midday and are highest downwind; surface P(O3) values are greater than vertically averaged values. Surface OPEs generally are highest downwind and peak during midday in downwind locations. In contrast, peaks occur in early morning and late afternoon in the vertically averaged case. Vertically averaged OPEs tend to be greater than those for the surface. Total reactivities are highest in upwind surface locations and peak during rush hours; vertically averaged reactivities are smaller and tend to be more uniform temporally and spatially. Total reactivity has large contributions from CO, alkanes, alkenes, aldehydes, unsubstituted monoaromatics, and secondary organics. Calculations using estimated emissions for 2010 result in decreases in P(O3) values and reactivities but increases in OPEs. PMID:14968859

  17. Adsorption energies of poly(ethylene oxide)-based surfactants and nanoparticles on an air-water surface.

    PubMed

    Zell, Zachary A; Isa, Lucio; Ilg, Patrick; Leal, L Gary; Squires, Todd M

    2014-01-14

    The self-assembly of polymer-based surfactants and nanoparticles on fluid-fluid interfaces is central to many applications, including dispersion stabilization, creation of novel 2D materials, and surface patterning. Very often these processes involve compressing interfacial monolayers of particles or polymers to obtain a desired material microstructure. At high surface pressures, however, even highly interfacially active objects can desorb from the interface. Methods of directly measuring the energy which keeps the polymer or particles bound to the interface (adsorption/desorption energies) are therefore of high interest for these processes. Moreover, though a geometric description linking adsorption energy and wetting properties through the definition of a contact angle can be established for rigid nano- or microparticles, such a description breaks down for deformable or aggregating objects. Here, we demonstrate a technique to quantify desorption energies directly, by comparing surface pressure-density compression measurements using a Wilhelmy plate and a custom-microfabricated deflection tensiometer. We focus on poly(ethylene oxide)-based polymers and nanoparticles. For PEO-based homo- and copolymers, the adsorption energy of PEO chains scales linearly with molecular weight and can be tuned by changing the subphase composition. Moreover, the desorption surface pressure of PEO-stabilized nanoparticles corresponds to the saturation surface pressure for spontaneously adsorbed monolayers, yielding trapping energies of ∼10(3) k(B)T. PMID:24328531

  18. Air stripping, oxidation, and activated-carbon adsorption studies for removal of taste and odor organics from water

    SciTech Connect

    Lalezary-Craig, S.

    1987-01-01

    A major class of water-consumer complaints are attributed to naturally occurring causatives of tastes and odors, among which a subgroup - the earthy-musty taste and odor compounds, documented to be spread worldwide - provides a special challenge to the scientific community and water utilities. The study was designed and executed to develop a firm basis for an understanding of the problem, as well as for optimization of process parameters for different-treatment techniques. The investigation began with determination of the physicochemical properties of a group of five earthy-musty taste and odor compounds including geosmin, 2-isobutyl-3-methoxy pyrazine (IBMP), 2-isopropyl-3-methoxy pyrazine (IPMP), 2-methylisoborneol (MIB), and 2, 3, 6-trichloroanisole (TCA). The second phase of the study investigated aeration, the application of oxidants such as chlorine, chlorine dioxide, and potassium permanganate, and several absorbents including manganese dioxide, kaolinite, and bentonite, for the mitigation of taste-and-odor problem. Other treatment processes investigated were ozonation and activated carbon adsorption. To investigate the efficiency of powdered activated carbon and closely simulate full-scale treatment operations, pilot-plant studies were conducted at one of the several plants operated by the Metropolitan Water District of Southern California.

  19. Identification of the Dinuclear and Tetranuclear Air-Oxidized Products Derived from Labile Phenolate-Bridged Dimanganese(II) Pyridyl-Chelate Compounds

    SciTech Connect

    Larsen,F.; Boisen, A.; Berry, K.; Moubaraki, B.; Murray, K.; McKee, V.; Scarrow, R.; McKenzie, C.

    2006-01-01

    Dioxygen-sensitive dinuclear manganese complexes of the phenoxo-hinged dinucleating ligand 2,6-bis{l_brace}[N,N{prime}-bis(2-picolyl)amino]methyl{r_brace}-4-tert-butylphenolato (bpbp{sup -}) containing exogenous labile THF, water and perchlorato ligands are described. The manganese(II) complexes [Mn{sub 2}(bpbp)(ClO{sub 4}){sub 2}(THF)]{sup +} (1) and [Mn{sub 2}(bpbp)(ClO{sub 4})(H{sub 2}O){sub 2}]{sup 2+} (2) have been isolated as the salts 1{center_dot}ClO{sub 4}{center_dot}THF{center_dot}3H{sub 2}O, 1{center_dot}B(C{sub 6}H{sub 5}){sub 4}{center_dot}4THF and 2{center_dot}(ClO{sub 4})2{center_dot}H{sub 2}O. Complexes 1 and 2 are spontaneously oxidised in air in solution and the solid state. The reaction products of the air oxidation in THF, water and methanol solutions are labile dinuclear Mn{sup II}-Mn{sup III}, Mn{sup III}{sub 2} and Mn{sup III}-Mn{sup IV} complexes containing water- and methanol-derived exogenous ligands. In addition, a Mn{sub 4} complex has been isolated. Magnetic susceptibility data confirm the Mn{sup II}-Mn{sup III} oxidation state assignment with an S = 2/S = 5/2 model with weak antiferromagnetic coupling (J = -3.7 cm{sup -1}) in [Mn{sub 2}(bpbp)(CH{sub 3}O){sub 2}(H{sub 2}O){sub 2}](ClO{sub 4}){sub 2} [3{center_dot}(ClO{sub 4}){sub 2}]. A tetranuclear complex, [Mn{sub 4}(O){sub 4-n}(OH){sub n}(bpbp){sub 2}](ClO{sub 4}){sub 4} [n = 1 or 2; 7{center_dot}(ClO{sub 4}){sub 4}], recovered from THF shows a Mn{sub 4}O{sub 6} adamantane-type core with the O bridges furnished by the two phenolato groups and four hydroxide/oxide bridges. We have arrived at two feasible formulations for the core metal oxidation states and oxo-bridge protonation states, namely [Mn{sup III}{sub 4}(O){sub 2}(OH){sub 2}(bpbp){sub 2}]{sup 4+} and [Mn{sup III}{sub 3}Mn{sup IV}(O){sub 3}(OH)(bpbp){sub 2}]{sup 4+}, for 7, on the basis of a bond valence sum analysis of the crystal structure, elemental analysis and XANES. Thus, complex 7 is at least two oxidation state levels

  20. Electronic environments in Ni{sub 3}Pb{sub 2}S{sub 2} (shandite) and its initial oxidation in air

    SciTech Connect

    Skinner, William M.; Qian, Gujie; Buckley, Alan N.

    2013-10-15

    Polycrystalline Ni{sub 3}Pb{sub 2}S{sub 2} (shandite) was synthesised as a non-porous ingot to enable representative surfaces prepared by fracture under UHV to be characterised by X-ray photoelectron spectroscopy (XPS) before and after exposure to air. For an unoxidised surface, the S 2p{sub 3/2} binding energy was found to be significantly lower than those reported previously for shandite itself and other sulfides having shandite structure, and consistent with the physical and chemical properties of the shandites. The core electron binding energies for the three constituent elements were in agreement with the formal oxidation state representation Ni{sup 0}{sub 3}Pb{sup II}{sub 2}S{sup −II}{sub 2}, analogous to that deduced previously for Ni{sub 3}Sn{sub 2}S{sub 2}. Shandite surfaces were found to oxidise rapidly when initially exposed to air under ambient conditions, and concomitant with the formation of the Ni–O and Pb–O species, to restructure to NiS- and PbS-like surface phases having S core electron binding energies no higher than those for shandite. - Graphical abstract: Shandite ingot fracture surface in sample holder. Display Omitted - Highlights: • Shandite synthesised as ingot so that fracture surfaces were representative of bulk. • Surfaces prepared by fracture in vacuum characterised by XPS. • S 2p{sub 3/2} binding energy in range expected and lower than reported previously. • Ni, Pb and S core electron binding energies consistent with Ni{sup 0}{sub 3}Pb{sup II}{sub 2}S{sup −II}{sub 2}.